iUUCD 2.0 - integrated annotations for ubiquitin and ubiquitin-like conjugation database

NEBL

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs11012539	snp	C/T	0.039522	0.134904	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21129428	CTTATTCTTAATTGA[C/T]CTTACAGAATTTTGT	10529
rs11012540	snp	C/T	0.185472	0.241529	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21129554	gcacactcatatatg[C/T]ttttgtataagtgaa	10529
rs11012541	snp	A/G	0.123105	0.215401	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21130834	CTTTAAGAAACTGGA[A/G]AAAGAAGAGCCAATT	10529
rs11012542	snp	C/G	0.189576	0.242588	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21135542	GCCAACAATCAGCCT[C/G]CTGCAACTCCAGGAA	10529
rs11012543	snp	A/G	0.190519	0.242821	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21139896	TGGCTCACGCCTGTA[A/G]TCCCAGCACTTTGGG	10529
rs11012545	snp	C/G/T	0.0023933	0.0345097	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21143373	agaatagcttgaacc[C/G/T]gggacgtggaggttg	10529
rs11012546	snp	A/G			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21144380	GCCCTACAAGGTAAC[A/G]CACCCTCCTTGGCCA	10529
rs11012547	snp	A/G	0.127599	0.217986	intron-variant	NEBL	GRCh38.p7	10:21154416	atgagctgaaatcgc[A/G]ccactgcactccatc	10529
rs11012548	snp	G/T	0.127254	0.217792	intron-variant	NEBL	GRCh38.p7	10:21157104	GTGAAAGAAGAGAAG[G/T]TTATTACTCCTTGAA	10529
rs11012549	snp	C/T	0.211212	0.246973	intron-variant	NEBL	GRCh38.p7	10:21157610	ATTGAATTTGTTTTA[C/T]AAAATTCTTCAGTTC	10529
rs11012550	snp	A/G	0.205417	0.245993	intron-variant	NEBL	GRCh38.p7	10:21161999	TTGGGGCTTTGAGCC[A/G]GATGAGATCAGCTGA	10529
rs11012551	snp	A/G	0.188946	0.24243	intron-variant	NEBL	GRCh38.p7	10:21162818	AATATCTTCACAAAG[A/G]TAGGCATAGCCTTAC	10529
rs11012552	snp	G/T	0.338069	0.233974	intron-variant	NEBL	GRCh38.p7	10:21164528	CCATGATTGAGGAGA[G/T]ATCTGCTGAGCTTCA	10529
rs11012553	snp	C/T	0.110872	0.20771	intron-variant	NEBL	GRCh38.p7	10:21166870	AGATAACTCAAGTCC[C/T]TGGAGTGTTCTAGAA	10529
rs11012554	snp	C/T	0.201418	0.245234	intron-variant	NEBL	GRCh38.p7	10:21168823	ggaggctgaggcggg[C/T]ggatcacaaggtcag	10529
rs11012555	snp	A/T	0.346811	0.230494	intron-variant	NEBL	GRCh38.p7	10:21170203	CCTTATCCAATTCTC[A/T]CTCATTGTTGTAATT	10529
rs11012556	snp	C/G	0.193028	0.243422	upstream-variant-2KB, intron-variant	NEBL, NEBL-AS1	GRCh38.p7	10:21175042	CCAAACCAGAAGAGC[C/G]AGAAAATCAAGTAGA	10529
rs11286684	in-del	-/A	0	0	intron-variant	NEBL	GRCh38.p7	10:20792124	CCAAATTCCAAATAG[-/A]AAAAAAAAAAAAAGA	10529
rs11289396	in-del	-/A			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21140007	AAAAAAAAAAAAAAA[-/A]TACAAAAATTAGGCG	10529
rs11298619	in-del	-/A	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20805853	GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAGT	10529
rs11307223	in-del	-/G	0.365646	0.221644	intron-variant	NEBL	GRCh38.p7	10:21153379	AGGCTGGAGTGCAAT[-/G]GTGAGATCTCAGCTC	10529
rs11311853	in-del	-/C	0.128632	0.218563	intron-variant	NEBL	GRCh38.p7	10:20933589	AAATACAAAAATTAG[-/C]CGGGTGTGGTGGCAC	10529
rs11314209	in-del	-/A	0.499642	0.0133738	intron-variant	NEBL	GRCh38.p7	10:21160865	CTTATTTCCAGGGGG[-/A]AAAAAAAAAAAAACA	10529
rs11315155	in-del	-/A	0.0298908	0.118541	intron-variant	NEBL	GRCh38.p7	10:21047641	TACATAGCATTGACC[-/A]AAAAAATGTGCAGGA	10529
rs11340674	in-del	-/G	0.0626037	0.165477	intron-variant	NEBL	GRCh38.p7	10:20802452	TGTTCTTAAATCAAA[-/G]TAACACAGTAGAGAT	10529
rs11342075	in-del	-/A	0.498034	0.0312882	intron-variant	NEBL	GRCh38.p7	10:21112742	AACTTAAAGTATAAT[-/A]AAAAAAAAAAAAGAA	10529
rs11345723	in-del	-/A	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20951398	GAAGAAAATATGAGC[-/A]AAAAAAAAAAAAGAA	10529
rs11345784	in-del	-/T			intron-variant	NEBL	GRCh38.p7	10:21074484	TTCTGAATTTTTTTC[-/T]TTTTTTTTTTTTTGA	10529
rs11353377	in-del	-/G	0.49533	0.0480965	intron-variant	NEBL	GRCh38.p7	10:21097220	CACTTTGGGAGGTCC[-/G]GGGGGGGGGTGGGGC	10529
rs11377677	in-del	-/T			intron-variant	NEBL	GRCh38.p7	10:20980316	AAAAAAGTTTTTTTT[-/T]GTTCCAGAACAAAAA	10529
rs11388003	in-del	-/A	0.316	0.241131	intron-variant	NEBL	GRCh38.p7	10:20955911	CAAAAAAAAAAAAAA[-/A]GTCATATGTGTTAAT	10529
rs11392907	in-del	-/A	0.436834	0.166111	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20868052	ATTTTATCTATATTA[-/A]AAAAAAAAAAAAAAC	10529
rs11399003	in-del	-/A	0.499363	0.0178419	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20898444	ACTGTAAAAAAAAAA[-/A]TGCCTTGGCCTTACC	10529
rs11400101	in-del	-/A	0.460252	0.135255	intron-variant	NEBL	GRCh38.p7	10:21089847	ACAGATGGGTTTTCC[-/A]AAAAACATGTCCATA	10529
rs11400880	in-del	-/G/T	0.375	0.216506	intron-variant	NEBL	GRCh38.p7	10:21091525	CCAATTAGCTATCAG[-/G/T]TACCTCAAGTTTCCT	10529
rs11410847	in-del	-/A	0	0	intron-variant	NEBL	GRCh38.p7	10:20909151	TTTGAGTTACAAACA[-/A]TCCAACTACACTCTT	10529
rs11413698	in-del	-/A	0.447926	0.169346	intron-variant, upstream-variant-2KB	NEBL, NEBL-AS1	GRCh38.p7	10:21172481	AATACTGGAAAAAAA[-/A]AAAAAAACATTTAAA	10529
rs11445710	in-del	-/T	0.129664	0.219133	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20851988	GCTGGAACTGACATC[-/T]TTTGCAACTATTTAA	10529
rs11450021	in-del	-/T	0.0410537	0.137264	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20783628	TATTTAGTCTGAAAA[-/T]TTTAATCAACAACTA	10529
rs11453441	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:20798110	AAAAAAAAAAAAAAA[-/A]TGTAGCATGGGCATA	10529
rs11453507	in-del	-/A	0.426966	0.176587	intron-variant	NEBL	GRCh38.p7	10:21064217	TTAACGTCAAAAAAA[-/A]TTGAATTCAAATGAA	10529
rs11492535	snp	A/C	0	0	intron-variant	NEBL	GRCh38.p7	10:20940284	GGATTAAGAAACTCA[A/C]TCAAAACCGCTCAAC	10529
rs11492536	snp	A/G	0.194902	0.243853	intron-variant	NEBL	GRCh38.p7	10:20940349	TACTGGGTACATAAC[A/G]AAATGAAGGCAGAAA	10529
rs11498224	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21077232	TTCTTCAAAAAAAAT[A/T]AAAAATCAAAGGAAT	10529
rs11511160	snp	C/T	0	0	intron-variant	NEBL	GRCh38.p7	10:20939437	CTCCTGAAGGAAGCA[C/T]GAAACTTGGAAAGGA	10529
rs11511164	snp	G/T	0.455383	0.142541	intron-variant	NEBL	GRCh38.p7	10:20941621	ATAAAGGGTATTCAA[G/T]TAGGAAAAGAGGAAG	10529
rs11523372	snp	G/T	0.18325	0.240924	intron-variant	NEBL	GRCh38.p7	10:21108013	TGGGATCGGTGGTGA[G/T]ATCCCCTTTATCATT	10529
rs11523840	snp	A/G	0.180383	0.240111	intron-variant	NEBL	GRCh38.p7	10:21107800	ATCCATCTGGTCTTG[A/G]CCTATTTTTGGTTGG	10529
rs11525254	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:20910828	GTGTTTTTCGTTTTT[G/T]TTTTTTTTTTTTTGG	10529
rs11556881	snp	A/T			utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20782212	CTATTCTATAGTAAT[A/T]TTTTATTACACATGA	10529
rs11556882	snp	A/G	0.103438	0.202533	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20782543	GATCTGGTTTTTCCA[A/G]TGTGCCACAGTCTTT	10529
rs11591355	snp	C/T	0.257918	0.249875	missense, intron-variant, utr-variant-3-prime	C10orf113, NEBL	GRCh38.p7	10:21126077	CCCCAACCAGCTTCC[C/T]GGGAGGCCTCAGGCC	10529
rs11591548	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21067218	ccttgtgatccgccc[A/G]cctcggcctcccaaa	10529
rs11591968	snp	G/T	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21097230	GGTCCGGGGGGGGGG[G/T]GGGGCAGATCACAAG	10529
rs11593484	snp	A/G			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21127368	aGTTTGTGACTTCTA[A/G]AGAAGTCCATTGCAA	10529
rs11594006	snp	A/G	0	0	intron-variant	NEBL	GRCh38.p7	10:20976375	gagatttctcaaaga[A/G]ctgaaaaatagaatt	10529
rs11594295	snp	A/T	0.133435	0.221162	intron-variant	NEBL	GRCh38.p7	10:20931270	TGCAATGAGATTTTT[A/T]AAAAAAAATCTTTGG	10529
rs11594318	snp	A/G	0.3744	0.216852	intron-variant	NEBL	GRCh38.p7	10:20806158	AGAGGTGATTAACTA[A/G]CAGCAGCAGGTTTTT	10529
rs11594954	snp	A/C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20807409	CATGTATTTTTACCC[A/C/G]CAATAAAACAACCAG	10529
rs11595730	snp	C/T	0.424193	0.179323	intron-variant	NEBL	GRCh38.p7	10:21002995	TCACAGGTATTTTCA[C/T]TATGTGGCTTTTTTT	10529
rs11595943	snp	A/C	0	0	intron-variant	NEBL	GRCh38.p7	10:21034527	CCTTGCAATACATAG[A/C]CTCTACTTATTTGAC	10529
rs11596224	snp	A/G	0.131038	0.219882	intron-variant	NEBL	GRCh38.p7	10:20931205	AAGTATGACAAAGAC[A/G]CACCATAATTCTCAA	10529
rs11597232	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:20816327	TACTTAAAGGTATTC[A/T]CCGTAGACTGGTACT	10529
rs11597712	snp	C/T	0.409041	0.192888	intron-variant	NEBL	GRCh38.p7	10:20786410	ATATAGGTTTCTGTA[C/T]CACTATGAGAGAAAT	10529
rs11598110	snp	C/G	0	0	intron-variant	NEBL	GRCh38.p7	10:21061997	TGAAATTTCCTACTG[C/G]CCAACACGCACAATG	10529
rs11598437	snp	A/G	0	0	intron-variant	NEBL	GRCh38.p7	10:20980156	TGGCTTAACTTGCTA[A/G]CAAATATTTGTGTGT	10529
rs11599453	snp	A/C	0.26818	0.249338	intron-variant	NEBL	GRCh38.p7	10:21064191	AAAATAGAAACACAG[A/C]ACATACTTAAATATA	10529
rs11599589	snp	A/G	0.308661	0.24302	intron-variant	NEBL	GRCh38.p7	10:21160848	GAAATGAAGCCATCA[A/G]ACTTATTTCCAGGGG	10529
rs11599771	snp	G/T	0	0	intron-variant	NEBL	GRCh38.p7	10:21114933	agtttaaatatatcg[G/T]catgctatttgtttt	10529
rs11812369	snp	A/T	0.02016	0.0983543	intron-variant	NEBL	GRCh38.p7	10:21162055	ggagattgaacaatc[A/T]catcaccaatgagtc	10529
rs11812577	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21166928	AAGGAAAATAGATGG[G/T]GGGAATACTCTCAGG	10529
rs11813157	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20977338	TTCGTTCCCCCATTT[C/T]TTAACCAATGTTTGA	10529
rs11813930	snp	A/G	0.0232847	0.105357	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21140503	TGTAATTAAGTTACA[A/G]ATTGAATGGATTAAT	10529
rs11813945	snp	C/T	0.298651	0.24522	intron-variant	NEBL	GRCh38.p7	10:20973650	GCCTCTTTCTCTTCA[C/T]GTAGACTTTGTCAAG	10529
rs11813989	snp	C/T	0.0142736	0.0832652	intron-variant	NEBL	GRCh38.p7	10:21039637	TAACTTAAAATGgtg[C/T]ttttaaaactttgat	10529
rs11814556	snp	A/G	0.0115144	0.0749975	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21131401	tcttacgacaccctc[A/G]ttgccctaatgccaa	10529
rs11815419	snp	C/G	0.0524604	0.153226	intron-variant	NEBL	GRCh38.p7	10:21151859	ATCTCTTCCCCTGCT[C/G]CATTTTTCTCTATAG	10529
rs11815878	snp	A/G	0.0501905	0.150254	intron-variant	NEBL	GRCh38.p7	10:21078808	CAGAGATATTTGGGC[A/G]AAGCACTAGAAGTTG	10529
rs11815973	snp	C/T	0.0622301	0.165053	intron-variant	NEBL	GRCh38.p7	10:20802512	ACATTGAAAAGTAGA[C/T]TGACAAGTAAAGAAA	10529
rs11816129	snp	A/G	0.0962929	0.197165	intron-variant	NEBL	GRCh38.p7	10:20799872	ATGGGATACATATAC[A/G]TGGTAAAATGGTTAC	10529
rs11816130	snp	A/G	0.367503	0.220665	intron-variant	NEBL	GRCh38.p7	10:21009392	ATCATGGATTCCTGT[A/G]AATAAGAAAAATTCC	10529
rs11816800	snp	A/G	0.0325976	0.123435	intron-variant	NEBL	GRCh38.p7	10:20801727	CCAGGGCAATTGGCC[A/G]CACAGTTGATGCACT	10529
rs11817086	snp	A/C/G	0.188631	0.242351	intron-variant	NEBL	GRCh38.p7	10:21148704	ctaatttttgtattc[A/C/G]tagtagagacagggt	10529
rs11817287	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20977804	AGTTTGCCCTAATAC[A/G]TTGCCAGGTTATGAA	10529
rs11817617	snp	A/C	0	0	intron-variant	NEBL	GRCh38.p7	10:21082173	agagtcgtgaaagtc[A/C]ccaagcaacgaagga	10529
rs11817725	snp	G/T	0.271162	0.249103	intron-variant	NEBL	GRCh38.p7	10:21079143	CAGCCTCTCTCTCTC[G/T]GAAACCTTCTCTATT	10529
rs11817951	snp	A/G	0.396727	0.202413	intron-variant	NEBL	GRCh38.p7	10:21009420	TCCACAGAAACAGGA[A/G]CTCAGTGTCAGTCAA	10529
rs11818498	snp	C/G	0.0182019	0.0936463	intron-variant	NEBL	GRCh38.p7	10:21156159	TGGCATTCATTTATT[C/G]GGGGACAGGAGGAAT	10529
rs11818826	snp	A/C	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20938499	ggggagacaccagag[A/C]agaaaagctgaaaat	10529
rs11819097	snp	A/G	0.140919	0.224948	intron-variant	NEBL	GRCh38.p7	10:21155287	agttacaaacaatcc[A/G]attatattctattag	10529
rs12098600	snp	G/T	0.179425	0.239831	intron-variant	NEBL	GRCh38.p7	10:20833419	AACATTGGTTGAAAA[G/T]GATCTGAGCCTGTCA	10529
rs12098681	snp	A/T	0.0509478	0.151255	intron-variant	NEBL	GRCh38.p7	10:20835355	AAGCAAAAACTGTAA[A/T]TTTTCAAACTGGCAT	10529
rs12217205	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21082812	ctgtcaccaaggcta[A/G]aatgcagtggcatat	10529
rs12217348	snp	A/G	0.170084	0.236883	intron-variant	NEBL	GRCh38.p7	10:20791743	TGGAAAAGAGGAAAT[A/G]TACGTAAATACACAA	10529
rs12217391	snp	C/G	0	0	intron-variant	NEBL	GRCh38.p7	10:20946714	TCCCGTTTTATTATT[C/G]TTTAAACTGGACATA	10529
rs12217594	snp	C/T	0	0	intron-variant	NEBL	GRCh38.p7	10:20946804	CTTAATATCAGGAGG[C/T]TGGAATCAGGGATTC	10529
rs12217637	snp	C/T	0.133093	0.220981	intron-variant	NEBL	GRCh38.p7	10:20947306	AGTATTCAGGCAGCA[C/T]AGATTTAAGATGAGA	10529
rs12218142	snp	G/T	0.204803	0.245881	intron-variant	NEBL	GRCh38.p7	10:21124227	GAGGAGGTAAAGCTT[G/T]TAGCATATTGATAGA	10529
rs12219100	snp	C/T	0.155987	0.23165	intron-variant	NEBL	GRCh38.p7	10:20977435	TCAAATTTCTAGTTA[C/T]AGTACAAATAGAGGT	10529
rs12219269	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21100743	TTTCCTTGTTGAACA[G/T]AGCTACTTCATTCTA	10529
rs12220495	snp	C/T	0.124837	0.216412	intron-variant	NEBL	GRCh38.p7	10:20820977	TCTGGCCTCTTTCCT[C/T]GATATGTAACTTTCT	10529
rs12220884	snp	C/G	0.275197	0.248727	intron-variant	NEBL	GRCh38.p7	10:21015783	CTCCCGAAGTGCTGG[C/G]ATTACAGGCATAAGC	10529
rs12220955	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:20992941	cgccaccacacccgg[C/G]taattttgtttttgt	10529
rs12220994	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21023393	TTCTTCTGCCATTTA[C/T]CTTTAATTTAAAATT	10529
rs12221281	snp	G/T	0.0452528	0.143452	intron-variant	NEBL	GRCh38.p7	10:21112429	aaaagttgagttcat[G/T]tcctttgcagggaca	10529
rs12240662	snp	C/T	0.0341408	0.126114	intron-variant	NEBL	GRCh38.p7	10:21015285	GCTCCCCTGCTTCAA[C/T]CACGGTAGCTCCATG	10529
rs12240878	snp	A/G	0.0707826	0.174302	intron-variant	NEBL	GRCh38.p7	10:20987968	gttacttccttatga[A/G]atgatataccatctt	10529
rs12240966	snp	C/T	0.13446	0.221699	intron-variant	NEBL	GRCh38.p7	10:20985707	TTATTTCCCACAATC[C/T]ACTAGTATGCAGCTA	10529
rs12241164	snp	A/T			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21126972	agagggagaccctgt[A/T]tcaaaaaaaaaaaaa	10529
rs12241391	snp	C/T	0.0325976	0.123435	intron-variant	NEBL	GRCh38.p7	10:21121185	CTCAAATGGCTTCAG[C/T]TCAAAGAAGGAAATG	10529
rs12241951	snp	C/T	0.0737376	0.17729	intron-variant	NEBL	GRCh38.p7	10:21100968	TCCATTCCCACACAT[C/T]GACCTTTCACGGGAA	10529
rs12242106	snp	A/G/T	0.0333695	0.124785	intron-variant	NEBL	GRCh38.p7	10:20821705	AGTAAGCCACATAAT[A/G/T]TCTACCGGAATGCCA	10529
rs12242114	snp	A/G	0.0295035	0.117819	intron-variant	NEBL	GRCh38.p7	10:20787896	GTTTTATGAAGGAGT[A/G]ATATTCAGCTGACTT	10529
rs12242158	snp	A/G	0.0329836	0.124112	intron-variant	NEBL	GRCh38.p7	10:20818075	TACTGTCTTCTGACC[A/G]TGGGGCTTCTCCCTT	10529
rs12242272	snp	A/G	0.0217236	0.101931	intron-variant, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20853151	ATTGAGAGGCACAAG[A/G]AAAATGTAAGAGAAA	10529
rs12243039	snp	A/C	0.113685	0.209567	upstream-variant-2KB, intron-variant	C10orf113, NEBL	GRCh38.p7	10:21147293	CTCAAAAACTAGGAA[A/C]CTTCGCCCAGTTTCT	10529
rs12243918	snp	A/G	0.0225045	0.103662	intron-variant	NEBL	GRCh38.p7	10:21123230	ACTGTTCTAGATCTT[A/G]CTCTGTACAAAGTCA	10529
rs12244585	snp	A/G	0.229136	0.249128	intron-variant	NEBL	GRCh38.p7	10:20789548	TGTTTTCTCATTTTG[A/G]CTTTCAAAAAATAAG	10529
rs12244707	snp	A/G	0.154661	0.231107	intron-variant	NEBL	GRCh38.p7	10:21023375	ATGCTTTGGGGAACA[A/G]CCTTCTTCTGCCATT	10529
rs12245833	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21123791	tatataattttatat[A/T]ttatataaatataCA	10529
rs12245978	snp	C/G	0.0217236	0.101931	intron-variant	NEBL	GRCh38.p7	10:20890399	ACCAATTAAGAAGTA[C/G]AGGCGAAATTAAATG	10529
rs12246471	snp	A/T	0.0248432	0.108648	intron-variant	NEBL	GRCh38.p7	10:21094647	agattgccctaatcc[A/T]ctccagcctggATTT	10529
rs12246854	snp	C/T	0.0146672	0.084371	intron-variant	NEBL	GRCh38.p7	10:21033110	GATCACGGGAATACA[C/T]AAACAAGGAAATGTG	10529
rs12247240	snp	A/G	0.0973687	0.197999	intron-variant	NEBL	GRCh38.p7	10:20893796	AGAGGGCAGAAAACT[A/G]CAGATTAGATCTAGC	10529
rs12247681	snp	A/G	0.496999	0.0386216	intron-variant	NEBL	GRCh38.p7	10:20829557	TAACCTGCACATTGT[A/G]CACATGTACCCTGAA	10529
rs12247910	snp	A/G	0.0298908	0.118541	intron-variant	NEBL	GRCh38.p7	10:20796133	ttttgggaggctgag[A/G]cgggcggatcatttg	10529
rs12247993	snp	C/G	0.029116	0.117091	intron-variant	NEBL	GRCh38.p7	10:20802774	GAACGAAAACTGTGA[C/G]TCTCATAACTGCCCA	10529
rs12248713	snp	C/T	0.292008	0.246445	intron-variant	NEBL	GRCh38.p7	10:21003804	TAGCCTTTGCTTAAA[C/T]TATTCAATTATTTTA	10529
rs12248941	snp	A/T	0.0737376	0.17729	intron-variant	NEBL	GRCh38.p7	10:21025529	AATATAGGAAAAGTT[A/T]TATGCAAATCACTAG	10529
rs12249267	snp	A/G	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:21046433	cattacatagtgtac[A/G]catgtatcaaaacat	10529
rs12250741	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21093177	TTTTCCATTTTAGCA[A/G]AGCCAAATGAAGATT	10529
rs12250750	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21093243	TGCCTGGGTGACTCA[A/G]AGGATAAGTATTTGG	10529
rs12250790	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21093263	TAAGTATTTGGGAAA[A/G]ACATGAATGGTAGTG	10529
rs12250797	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21093297	GGGTCCACCAGCCCA[A/G]AAGCATTGGACGCAT	10529
rs12250854	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21093375	AAGAAATGGGCTGGA[A/G]AAGGGAGACTGTCAT	10529
rs12251227	snp	A/G	0.141596	0.225274	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20897809	TATTAGCTGATTAGA[A/G]GCTACTTATTTATTA	10529
rs12251286	snp	A/G	0.141258	0.225111	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20897933	AACATCATTAAACAT[A/G]AGAAGTTGCAGTTAA	10529
rs12251534	snp	A/C	0.107341	0.205301	intron-variant	NEBL	GRCh38.p7	10:20934923	TCTAGGACAGTATCA[A/C]GATAGGTCAAGAGTT	10529
rs12252643	snp	C/T	0.0158469	0.0875917	intron-variant	NEBL	GRCh38.p7	10:20901230	TCACTTGCTTATTTA[C/T]AATTCAGAAGTCTTC	10529
rs12252686	snp	A/G	0.0248432	0.108648	intron-variant	NEBL	GRCh38.p7	10:21093944	AGAAAACATTTTGTC[A/G]TTTTTGTGAAAGACT	10529
rs12252931	snp	A/G	0.0298908	0.118541	intron-variant	NEBL	GRCh38.p7	10:20806798	AATGATGGACTGAGG[A/G]GGATAGACATGAAGT	10529
rs12253841	snp	C/G	0	0	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21140263	ATTTTAGATGTGATT[C/G]AGTAAACAGTGAAAA	10529
rs12254313	snp	A/G	0.0236746	0.106192	intron-variant	NEBL	GRCh38.p7	10:20829427	aacatcacactctgg[A/G]gactgttgtggggta	10529
rs12255059	snp	C/T	0	0	intron-variant	NEBL	GRCh38.p7	10:20952616	CACTAAAGAAACTAG[C/T]TCATCTGTCAgggta	10529
rs12255274	snp	A/G	0.0452528	0.143452	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21143978	AAAAAAGAAATGATG[A/G]TTATTCGAATAAGAT	10529
rs12255487	snp	C/T	0.0217236	0.101931	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20852312	AATTATGTGAATTAA[C/T]GGTTATTTTACAAAA	10529
rs12255640	snp	A/G	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20802929	TTCTTGTTCTGCGCC[A/G]TTCTTATGACAGATG	10529
rs12255917	snp	A/G	0.112983	0.209108	intron-variant	NEBL	GRCh38.p7	10:20900691	AAAAAAAAATTAGCC[A/G]AGTGTGATGGCAGTA	10529
rs12256471	snp	A/G	0.0722614	0.17581	intron-variant	NEBL	GRCh38.p7	10:21006258	catccttgtacttac[A/G]ctttctatgctgata	10529
rs12257507	snp	C/G	0.379942	0.213577	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20846687	CTCTAGGCTAAAAAG[C/G]ACTCTTTAAATGGTG	10529
rs12257662	snp	A/C	0.0333695	0.124785	intron-variant	NEBL	GRCh38.p7	10:20818558	AGAATGCCAGTCAAG[A/C]CAGGTCTTCTTTTGC	10529
rs12257745	snp	A/G	0.140919	0.224948	intron-variant	NEBL	GRCh38.p7	10:20901336	CTCAGAGACACAGCC[A/G]TGGCCAAGGGAACGT	10529
rs12258051	snp	A/G	0.039522	0.134904	intron-variant	NEBL	GRCh38.p7	10:20806681	TAAGCCCCTTACAGC[A/G]GATGCATGTTTCTTT	10529
rs12258290	snp	C/T	0.0726307	0.176182	intron-variant	NEBL	GRCh38.p7	10:20989263	TACCTAGTTTAAAAA[C/T]ATATTTAATCCAACT	10529
rs12259297	snp	C/T	0.0217236	0.101931	intron-variant	NEBL	GRCh38.p7	10:20833979	GGCGCCATTTGAAGA[C/T]TGGGGAAAGCTAACC	10529
rs12259450	snp	A/C	0.148996	0.228688	intron-variant	NEBL	GRCh38.p7	10:20914203	TAGCTGTGGATAATT[A/C]GATGTCAGTAAGTGC	10529
rs12259657	snp	A/T	0.0916144	0.193427	intron-variant	NEBL	GRCh38.p7	10:20804518	CAAGCACCGTTCCAC[A/T]TAAGAGAGGGTGAAT	10529
rs12260294	snp	C/T	0.0236746	0.106192	intron-variant	NEBL	GRCh38.p7	10:21020303	TTTTCCCAACCCCAT[C/T]ACAGTGGAAGAGGGA	10529
rs12260634	snp	C/T	0.0225045	0.103662	intron-variant	NEBL	GRCh38.p7	10:21086447	ACTGCAGCCAATGAA[C/T]GATATAGAGAATTTC	10529
rs12260681	snp	A/T	0.0894459	0.191631	intron-variant	NEBL	GRCh38.p7	10:20935031	CGTTAAAACACTTAC[A/T]GAAGGCCAATACATG	10529
rs12260966	snp	C/T	0.021333	0.101051	intron-variant, upstream-variant-2KB	NEBL, LOC102725112	GRCh38.p7	10:20845179	GAAACACTGAATTAG[C/T]AGAGAATTAGGTAAA	10529
rs12261038	snp	C/T	0.0437281	0.141251	intron-variant	NEBL	GRCh38.p7	10:20935577	GCAATGAGAGACTGA[C/T]TCTGGAATCTGTGCC	10529
rs12261143	snp	A/G	0	0	intron-variant	NEBL	GRCh38.p7	10:21003169	TTCATAAAATCCCTA[A/G]ACCACAGCTCTTCTG	10529
rs12261351	snp	A/G	0	0	intron-variant	NEBL	GRCh38.p7	10:21003512	CTATTTTCTGAACCA[A/G]ATTATTCTTCAAAGA	10529
rs12261588	snp	A/G	0.305186	0.243833	intron-variant	NEBL	GRCh38.p7	10:21149480	atttttagtagatac[A/G]gggtttcaccatgtt	10529
rs12262319	snp	C/T	0.0225045	0.103662	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20850983	TGCTGAATTTTTTCA[C/T]AGACACTGAGTAAAA	10529
rs12262915	snp	C/T			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21126914	cagggcggggaagtt[C/T]tagtgagcagagatc	10529
rs12263258	snp	A/T	0.37138	0.218556	intron-variant	NEBL	GRCh38.p7	10:21058489	GGAAAGAAAAAGAAC[A/T]AGTTGAAAACCTATA	10529
rs12263514	snp	C/T	0.0240643	0.107019	intron-variant	NEBL	GRCh38.p7	10:21091844	gctatcttaccctgg[C/T]tgatcttgaactcct	10529
rs12263824	snp	C/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21092322	ATATCTAGTACTATC[C/T]CACTGTTTGCCTGTG	10529
rs12265374	snp	C/G	0.0162398	0.0886349	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20862496	GTGAGTCACATCACT[C/G]ACCTTCGGACTTGTT	10529
rs12265433	snp	C/T	0.030665	0.119967	intron-variant	NEBL	GRCh38.p7	10:20892672	CCCTCACCCACAAAT[C/T]CCACGTCTCCATTAC	10529
rs12265517	snp	A/G	0	0	intron-variant	NEBL	GRCh38.p7	10:21056006	GTTCATCCCAATGCA[A/G]ACCAGTGAACTATAT	10529
rs12265978	snp	A/C	0.107341	0.205301	intron-variant	NEBL	GRCh38.p7	10:20989534	GATGAATAAACAACC[A/C]AAAGAAACCATAAAT	10529
rs12266286	snp	C/T	0.0217236	0.101931	intron-variant	NEBL	GRCh38.p7	10:20888730	TCTAAAGACAAACAC[C/T]CTTTCCTCTTGGGAA	10529
rs12266414	snp	C/T	0	0	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20867829	atcatatattaaatt[C/T]ttatacatactggaa	10529
rs12266744	snp	A/G	0.0217236	0.101931	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20855793	CTCTTTAGAGTTTGG[A/G]TTAAAATAAAAGTAA	10529
rs12267369	snp	A/G	0.0441095	0.141807	intron-variant	NEBL	GRCh38.p7	10:20815903	cctcccaggtagctg[A/G]gattacaggcacctg	10529
rs12268357	snp	G/T	0.0792508	0.182605	intron-variant	NEBL	GRCh38.p7	10:20987155	CTATCTGTACCGACC[G/T]TTATGGGTAAACCTA	10529
rs12268405	snp	C/T	0.0517044	0.152246	intron-variant	NEBL	GRCh38.p7	10:21023878	TTGGATAGTAATGAA[C/T]TTCACTTGCTGCCCA	10529
rs12268690	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20869107	TAGCTTTTATAGTTT[C/T]GTTTATTCTCAGGAA	10529
rs12268894	snp	A/G	0.0248432	0.108648	intron-variant	NEBL	GRCh38.p7	10:21096537	tgtgtgttttgagac[A/G]gggtctcagtctgtc	10529
rs12269702	snp	A/C/G	0.0197687	0.0974348	intron-variant	NEBL	GRCh38.p7	10:20912406	caatgcgctacgatc[A/C/G]tgccactgcactcca	10529
rs12354449	snp	C/T	0.481319	0.0948228	intron-variant	NEBL	GRCh38.p7	10:20919921	CAGGGGGAAATTGCA[C/T]CATGAAGGGCTAAGA	10529
rs12354597	snp	A/T	0	0	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20860686	TTTGTTCTCTCATAA[A/T]ATTTTTCTGATGTTA	10529
rs12355488	snp	A/T	0.116488	0.211364	intron-variant	NEBL	GRCh38.p7	10:21098741	AGAAAACAAAAAAAA[A/T]TAAGGAAGTCCTCCT	10529
rs12355662	snp	A/G	0	0	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20860633	ACTTACTGTAGCCAG[A/G]AAAGGGTGTATTGAT	10529
rs12355782	snp	A/G	0.499017	0.0221427	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20855553	AAGGAAAACTTAATT[A/G]AATTAAGATCTGCAA	10529
rs12355975	snp	C/T	0.118933	0.212888	intron-variant	NEBL	GRCh38.p7	10:20793120	CTCTAGATTTTAGTT[C/T]GCAGATTCTTAATTA	10529
rs12355998	snp	A/G	0	0	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20860781	AGGCTCTGCTTTGCA[A/G]AAGACTTTATTAAAA	10529
rs12355999	snp	A/G	0	0	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20860784	CTCTGCTTTGCAGAA[A/G]ACTTTATTAAAAAGC	10529
rs12356048	snp	A/G	0.468349	0.121752	intron-variant	NEBL	GRCh38.p7	10:20921354	AGACCCTGAACCTGA[A/G]CACTGCATCTCCTGG	10529
rs12356151	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21121938	ATATACCAATATTAA[A/G]GAAGTTAACAGGTAA	10529
rs12356574	snp	C/T	0.126909	0.217598	intron-variant	NEBL	GRCh38.p7	10:21075231	TAATATTTTGTGCTA[C/T]AAACCCAAGAACGGC	10529
rs12356595	snp	A/G	0.0681886	0.171594	intron-variant	NEBL	GRCh38.p7	10:20792072	AAAGGTGAAGGTTTT[A/G]AAGGCCCCTCAATGA	10529
rs12357297	snp	A/G	0	0	intron-variant	NEBL	GRCh38.p7	10:20923830	TATCAACACAAGGCA[A/G]ACCCTTGACTTAGAG	10529
rs12358463	snp	A/T	0.334642	0.235236	intron-variant	NEBL	GRCh38.p7	10:21111677	ttcaggacataggca[A/T]gggcaaagactccat	10529
rs12358511	snp	C/G	0	0	intron-variant	NEBL	GRCh38.p7	10:21114862	tctgacagagcctgt[C/G]ttttaattgacagag	10529
rs12358522	snp	C/T	0	0	intron-variant	NEBL	GRCh38.p7	10:21114957	ttgttttctattttt[C/T]caagctgttctttgt	10529
rs12358829	snp	A/T	0	0	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20781326	GCAAATTAATCATCA[A/T]CCACAATTCTACATA	10529
rs12358990	snp	C/G	0	0	intron-variant	NEBL	GRCh38.p7	10:21049498	CACCACATCACTCCA[C/G]AGCCTAGAATGTCAT	10529
rs12359024	snp	A/G	0.416055	0.186885	intron-variant	NEBL	GRCh38.p7	10:20952387	GGTTGCCATGAGCCG[A/G]AATTGTACCACTGCA	10529
rs12359123	snp	A/G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21044451	CTGCAAGATTTCTCA[A/G/T]ATTTGGTCCTCTTTT	10529
rs12359138	snp	C/T	0.298651	0.24522	intron-variant	NEBL	GRCh38.p7	10:20921132	AAGTTATGCCTTTTC[C/T]TAACTCAGGAAACAA	10529
rs12359172	snp	C/T	0.14665	0.227637	intron-variant	NEBL	GRCh38.p7	10:20796239	GTAGTGGTGGGCGCC[C/T]GTTATCCCAGCTTCT	10529
rs12359227	snp	A/G	0.131038	0.219882	intron-variant	NEBL	GRCh38.p7	10:20811982	GGATTTCTCCTGACT[A/G]TAAGGAACAGATAGC	10529
rs12411391	snp	A/G	0.0150606	0.0854603	intron-variant	NEBL	GRCh38.p7	10:20812201	TCAACAGAACAACAC[A/G]TCAACCAAGCAGAAA	10529
rs12411671	snp	C/T	0.0908922	0.192833	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20961387	CTTAACTTTCAAGTT[C/T]CTTATTTTAATTATA	10529
rs12412142	snp	C/T	0.00943375	0.0680285	intron-variant	NEBL	GRCh38.p7	10:20947655	GCTATTTACAAATCA[C/T]AGCCATTGACATTTT	10529
rs12414264	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21033856	TAAAACTACATCTTC[A/C]AATAAATTATTTCTT	10529
rs12414680	snp	G/T	0.188316	0.242271	intron-variant	NEBL	GRCh38.p7	10:20944667	AGGCTTGTATCACAG[G/T]TGGAGCGTGAGCACA	10529
rs12569976	snp	A/T	0.385359	0.210185	intron-variant	NEBL	GRCh38.p7	10:20836830	tctgcaagcctaaat[A/T]ttcatggccatggga	10529
rs12570186	snp	A/T	0	0	intron-variant	NEBL	GRCh38.p7	10:20828359	AAATAATGAAAAATG[A/T]TAATTTGTAAAAATT	10529
rs12570525	snp	A/T	0.00966161	0.0688292	intron-variant	NEBL	GRCh38.p7	10:20999602	agaccctgtctcacc[A/T]cacaaaagaaaaaag	10529
rs12571375	snp	A/C			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21143409	agctgagatagcacc[A/C]ctgcactccagctgg	10529
rs12571783	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20894880	cttgcagtgagccga[A/G]atcgtgccactgccc	10529
rs12571856	snp	C/T	0.394904	0.203722	intron-variant	NEBL	GRCh38.p7	10:20807916	ACAGAAAACAGAAGA[C/T]ACAGGAAAAGAGTGG	10529
rs12572453	snp	C/T	0.00952359	0.0683454	intron-variant	NEBL	GRCh38.p7	10:21085917	AAAAATGTTTAGATA[C/T]ACAGGAGGAGCTTTT	10529
rs12572902	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21067110	cccgagtagctggga[C/T]tacaggcgcccgcca	10529
rs12573237	snp	C/G	0.459574	0.136304	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21128677	AAAAAAAAGGAAGAC[C/G]AACAAGAGAACATCA	10529
rs12573542	snp	A/C	0	0	intron-variant	NEBL	GRCh38.p7	10:21019940	TCAGGACAATTCAAG[A/C]CCGGGAACAGTACAG	10529
rs12762307	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20921484	caccctcccttctct[A/G]gagttctttctctgc	10529
rs12764367	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:20820152	TTTAGTGATAGACTA[G/T]TACTGTATAAAGAAA	10529
rs12766176	snp	C/T	0	0	intron-variant	NEBL	GRCh38.p7	10:20997279	CCCTGCCCTCTCAAT[C/T]TCTGACCACAGCCAG	10529
rs12766177	snp	C/T	0	0	intron-variant	NEBL	GRCh38.p7	10:20997281	CTGCCCTCTCAATCT[C/T]TGACCACAGCCAGTA	10529
rs12766546	snp	A/T	0	0	intron-variant	NEBL	GRCh38.p7	10:21076480	aaaaaaaaaagaatt[A/T]ccacacaacccaaca	10529
rs12766953	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20997287	TCTCAATCTCTGACC[A/C]CAGCCAGTAACAGTC	10529
rs12768678	snp	A/T	0	0	intron-variant	NEBL	GRCh38.p7	10:20795852	AATATATGAAAGATT[A/T]AGTTGAAAATACAAT	10529
rs12769129	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20900862	aaaaaaaagaaaaaa[A/G]aaaaaaattagccgg	10529
rs12770568	snp	C/T	0.47614	0.106587	intron-variant	NEBL	GRCh38.p7	10:20930973	AAACATAGAAACAAA[C/T]GCCTGTACCTTTACT	10529
rs12771271	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20900863	aaaaaaagaaaaaag[A/G]aaaaaattagccggg	10529
rs12771560	snp	G/T	0	0	intron-variant	NEBL	GRCh38.p7	10:21116293	ccaattcatttcctg[G/T]tgagagccctctttt	10529
rs12771970	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21100828	TGCTTCACAAAATTG[G/T]AAAAGTGAAGTACTC	10529
rs12772787	snp	A/T	0	0	intron-variant	NEBL	GRCh38.p7	10:20792122	GGCCAAATTCCAAAT[A/T]Gaaaaaaaaaaaaaa	10529
rs12773526	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21071982	tgccaccacacccag[C/T]taatttttgtgtttt	10529
rs12774314	snp	A/G	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:20963548	ATTCTAGAATCATAG[A/G]TATTTTTGGTTTTTT	10529
rs12776873	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:20901026	ccctcttaaaaaaaa[A/T]aaaaagaaaaaGCAC	10529
rs12777460	snp	A/G	0	0	intron-variant	NEBL	GRCh38.p7	10:20950752	CATCAAAGGCCTCAC[A/G]CAATTACACAACAAA	10529
rs12777530	snp	C/T	0.202959	0.245534	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20856052	GTATACAGCTTTATA[C/T]AATGTACACAACTTT	10529
rs12777608	snp	A/C	0	0	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20847655	GGGCAGGGGAGGAAA[A/C]TAGAAGGAGGTCCAG	10529
rs12779051	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:21166139	gcaggagaatggcgt[C/G]aatccgggaggcgga	10529
rs12779119	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21071752	aacaacagaaattta[G/T]tcttttgcagttcca	10529
rs12779334	snp	G/T	0	0	intron-variant	NEBL	GRCh38.p7	10:21116398	cttcttcttataaag[G/T]tattaatcttatcat	10529
rs12782552	snp	A/T	0.0256215	0.110247	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21139612	TGGACATATGGTTCC[A/T]CAACCCCAAATCTCT	10529
rs12783594	snp	C/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20847656	GGCAGGGGAGGAAAC[C/T]AGAAGGAGGTCCAGC	10529
rs12784374	snp	A/C	0.00980368	0.0693234	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20878709	AAACACTTTCTAAAT[A/C]CTATTATATGTACAA	10529
rs12784785	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20895789	AAGAGCCAGTCATAT[C/T]TAAATTGTGATTGGA	10529
rs12784899	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20952434	agcgtgagactctgt[C/T]tgaaggaaaaaaaaa	10529
rs12784926	snp	A/C	0.00318978	0.0398085	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20785161	TAAATAGATACCAGT[A/C]AGCCTAGGGAACAAG	10529
rs16905928	snp	A/G	0.126564	0.217402	intron-variant	NEBL	GRCh38.p7	10:20951889	TGCACTGGAAATTGA[A/G]ACGTGAAGCTAGTCT	10529
rs16916070	snp	A/C	0.273856	0.248859	intron-variant	NEBL	GRCh38.p7	10:21057389	TCAAAGGGACCTTGC[A/C]CATATCAAAGAAACA	10529
rs16921055	snp	A/G	0.030665	0.119967	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20782056	ATAGCTCAACTCTAT[A/G]TAAATCCACAAAGAA	10529
rs16921056	snp	C/T	0.0295035	0.117819	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20784259	TCACAGTAAACGGCA[C/T]AATCAGAAAAACACA	10529
rs16921058	snp	C/T	0.0869089	0.189476	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20785091	GAACTGAGCATAGAC[C/T]TGGGTCCATAGAATA	10529
rs16921130	snp	A/G	0.0821764	0.185298	intron-variant	NEBL	GRCh38.p7	10:20825933	AGCAGAAGGTAAAAC[A/G]GGCTGGAAAGAAGAA	10529
rs16921131	snp	G/T	0.00914312	0.0669923	intron-variant	NEBL	GRCh38.p7	10:20842447	AATGCAATGTCAATG[G/T]AAAAACCACAAAGTA	10529
rs16921139	snp	A/G	0.381308	0.21274	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20847515	ATTTATCAGTGAAAG[A/G]AAAGTTATCCACAGA	10529
rs16921160	snp	A/T	0.00953873	0.0683987	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20856397	GAAATTACCACCATG[A/T]TATTTTTATTGGCTT	10529
rs16921162	snp	C/T	0.00953873	0.0683987	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20856445	CATGTCCCTAGGAAA[C/T]TGAATTTAAGTATGG	10529
rs16921165	snp	C/T	0.0170251	0.090679	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20857775	TGACAAGACTAAAAG[C/T]GATGTGTCAATGCAG	10529
rs16921170	snp	A/G	0.0166325	0.0896639	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20862299	TCAGTACAGTGAGTG[A/G]TTTGATTCAAGATGC	10529
rs16921209	snp	C/G	0.0955749	0.196603	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20879174	ACTAATTGACAGTAA[C/G]CTTTAAGGTGGAGAC	10529
rs16921211	snp	A/G	0.00874735	0.0655527	intron-variant, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20879922	CATGCAAACCTTGAT[A/G]CAACTGCTAACTTTT	10529
rs16921213	snp	G/T	0.126909	0.217598	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20880994	AGGACTTTATATATT[G/T]GAATACCACCACTGA	10529
rs16921216	snp	A/G	0.039522	0.134904	intron-variant, downstream-variant-500B	NEBL, LOC102725112	GRCh38.p7	10:20885279	AGGTAAACTCTAAGA[A/G]TCACAATTTTAACAA	10529
rs16921218	snp	A/G	0.0402882	0.136092	intron-variant, downstream-variant-500B	NEBL, LOC102725112	GRCh38.p7	10:20885361	ATCTTTGAAGTAGCC[A/G]CCTTATTCAAAGTCT	10529
rs16921221	snp	A/T	0.039522	0.134904	intron-variant	NEBL	GRCh38.p7	10:20885895	CGTTGACATCATATA[A/T]TTTAAGCTGCATGTT	10529
rs16921225	snp	C/T	0.0810805	0.184299	intron-variant	NEBL	GRCh38.p7	10:20887831	TTTCATCCATGTAAG[C/T]TGTCTAAATGAGATT	10529
rs16921227	snp	C/T	0.103082	0.202275	intron-variant	NEBL	GRCh38.p7	10:20889339	TAGCGTATTCCTCAG[C/T]CTGTGATTTTATAAT	10529
rs16921232	snp	C/T	0.13875	0.223883	intron-variant, synonymous-codon, nc-transcript-variant	NEBL	GRCh38.p7	10:20897191	TTTTATATCCTCAAA[C/T]ACAGGGACCCTCATT	10529
rs16921240	snp	C/T	0.209084	0.246629	intron-variant	NEBL	GRCh38.p7	10:20907637	TCACCAGGAAGTATA[C/T]GAGATTTTTAATAAA	10529
rs16921248	snp	C/G	0.181659	0.240478	intron-variant	NEBL	GRCh38.p7	10:20910523	GAGATGTGAAGGCAG[C/G]TAAACCCTCACTGCA	10529
rs16921251	snp	C/T	0.152001	0.229992	intron-variant	NEBL	GRCh38.p7	10:20912669	AGCATTTCCTACTTA[C/T]GTTGCACCTAGATTA	10529
rs16921283	snp	A/G	0.0554779	0.157039	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20958171	AGAAAAGGGTGTTTC[A/G]TTTTTTTTAATGCCC	10529
rs16921284	snp	A/G	0.0193772	0.0965046	intron-variant	NEBL	GRCh38.p7	10:20962553	TTTTACTGTTTCCTC[A/G]GAGGACTGGAACAGC	10529
rs16921286	snp	C/T	0.151668	0.229849	intron-variant	NEBL	GRCh38.p7	10:20970254	ACACATGTTGACTCA[C/T]TCACTCATCATAACT	10529
rs16921300	snp	A/T	0.0528381	0.153711	intron-variant	NEBL	GRCh38.p7	10:20975512	TACATCAGTAGCAAG[A/T]GCTATTATAGGGATT	10529
rs16921329	snp	C/T	0.081446	0.184634	intron-variant	NEBL	GRCh38.p7	10:20982117	ATCAACGTTCAATTA[C/T]CCACCCTAACAGAAA	10529
rs16921338	snp	C/G	0.0726307	0.176182	intron-variant	NEBL	GRCh38.p7	10:20983271	AAATTAACCATGAAA[C/G]ATAGAACAATTATCT	10529
rs16921350	snp	A/G	0.0501905	0.150254	intron-variant	NEBL	GRCh38.p7	10:20986208	ATATAACCAGGAAAT[A/G]TCATACCATATATAT	10529
rs16921362	snp	A/G	0.0387552	0.1337	intron-variant	NEBL	GRCh38.p7	10:20995127	TTTGAAGCAAAGTCT[A/G]AACGTCAGGACAGGG	10529
rs16921366	snp	A/G	0.0718919	0.175435	intron-variant	NEBL	GRCh38.p7	10:20998694	GCACACAGCAATAAT[A/G]CTATCCAATCTGCAT	10529
rs16921398	snp	C/T	0.163892	0.234703	intron-variant	NEBL	GRCh38.p7	10:21002079	GAGATGAAAGGTACT[C/T]GCTCGATGTAAATGT	10529
rs16921408	snp	A/G	0.0584853	0.160693	intron-variant	NEBL	GRCh38.p7	10:21006886	ATTTTAAGAAGGAGC[A/G]AGTTCTATAAATAGT	10529
rs16921415	snp	A/C	0.396	0.202938	intron-variant	NEBL	GRCh38.p7	10:21010131	AATAGTTCCCTAATG[A/C]GCCTGTTAATTTAAT	10529
rs16921434	snp	A/G	0.0471551	0.14613	intron-variant	NEBL	GRCh38.p7	10:21025633	AAGAACATGACTGGG[A/G]AGAGCGAGAACCCAG	10529
rs16921469	snp	A/G	0.00676609	0.0577691	intron-variant	NEBL	GRCh38.p7	10:21048404	AAATCTCCCGGGGCG[A/G]TCTTCTTCCAAGGGC	10529
rs16921472	snp	A/G	0.0341408	0.126114	intron-variant	NEBL	GRCh38.p7	10:21049381	GAAGAAAGTTTATCA[A/G]TTCATTGTAGATTTG	10529
rs16921476	snp	A/G	0.0726307	0.176182	intron-variant	NEBL	GRCh38.p7	10:21052901	CCACATAAATAATTC[A/G]CTGACATACAATTAA	10529
rs16921489	snp	C/T	0.463018	0.130857	intron-variant	NEBL	GRCh38.p7	10:21054649	TGAAAGGAAGGACCA[C/T]AGCACAAATGTATTT	10529
rs16921507	snp	C/T	0.0341408	0.126114	intron-variant	NEBL	GRCh38.p7	10:21057077	AAAGCAAAATAGTCA[C/T]ATATACAAGTGGCCA	10529
rs16921520	snp	A/G	0.0341408	0.126114	intron-variant	NEBL	GRCh38.p7	10:21060407	AGATTACCTGGAATG[A/G]TGGTTCTCAAACTTG	10529
rs16921538	snp	A/G	0.0752113	0.178743	intron-variant	NEBL	GRCh38.p7	10:21077892	TGGGCTTCCCACACT[A/G]TTCATGACCACGAGA	10529
rs16921580	snp	C/T	0.40733	0.194287	intron-variant	NEBL	GRCh38.p7	10:21099821	TTGCACACTCCTCTG[C/T]TGAACAAGGCCAAAG	10529
rs16921632	snp	C/T	0.0228947	0.104514	intron-variant	NEBL	GRCh38.p7	10:21161398	GGCTAAGCTGTATCA[C/T]TCAGACAGCCAAAAG	10529
rs17738142	snp	C/T	0.0569829	0.158885	intron-variant	NEBL	GRCh38.p7	10:20980246	TCATCAGTGAATGGG[C/T]TAAGCCATACTTTTG	10529
rs17797263	snp	A/G	0.00755907	0.0610114	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20863292	CTGTGACTCAGAATC[A/G]CAAAAAGCCAGCAAA	10529
rs17810580	snp	C/T	0.00835141	0.0640778	intron-variant	NEBL	GRCh38.p7	10:20964149	TCCAATCTCATGTGG[C/T]CCCTTTGCCCTCACA	10529
rs17810616	snp	A/G	0.0150606	0.0854603	intron-variant	NEBL	GRCh38.p7	10:20968568	TCATAGAAGTTCAAG[A/G]GGATGCGTCGCATGT	10529
rs17811177	snp	G/T	0.0562307	0.157967	intron-variant	NEBL	GRCh38.p7	10:20983227	TAGAATGCTGAGACT[G/T]TACGATTCATTCCAG	10529
rs17813705	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21084964	TTTAGAAAAGAGACC[A/G]GTGGGTTAGTGCGGA	10529
rs17813896	snp	C/T	0.0197687	0.0974348	intron-variant	NEBL	GRCh38.p7	10:21090721	AGGAAGCTGAATGGC[C/T]GCCCTATCGCCACCT	10529
rs17814015	snp	A/C	0.0240643	0.107019	intron-variant	NEBL	GRCh38.p7	10:21102180	TACTTAAATGTTTCA[A/C]CAAAGGCAGAAGTTA	10529
rs28364728	snp	A/G	0.0189856	0.0955633	intron-variant	NEBL	GRCh38.p7	10:20786741	AAACTTGGAAGAAGT[A/G]TTCAACATTTGCTAG	10529
rs28380212	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20789939	TGTGTATATGTGTAT[A/G]TATATATGTGTGTGT	10529
rs28411207	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21061292	TTATGTGATATGTAA[C/T]ATATTACATATTATG	10529
rs28425649	snp	A/G	0.489665	0.0711382	intron-variant	NEBL	GRCh38.p7	10:20789929	TATATATGTGTGTGT[A/G]TATGTGTATATATAT	10529
rs28577237	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21061329	GTAATATATTACATA[A/T]TATGTGATATGTAAT	10529
rs28608182	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21061432	TCATATATTGCATGG[G/T]GTATGATATATATCG	10529
rs28613816	snp	C/T	0.021333	0.101051	intron-variant	NEBL	GRCh38.p7	10:20910673	CTACACTGTAAAAAA[C/T]TAGACCAATCTTCCT	10529
rs28710249	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20980391	AAGAACCAGAAAAAG[A/G]AAAAAAAATATATTT	10529
rs28848250	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21109491	TCTGCCAGGTTTTGG[G/T]GTCAGGATGATGCTG	10529
rs33932343	snp	A/G	0.498908	0.0233371	intron-variant	NEBL	GRCh38.p7	10:20955158	AATTAGAGAGGTGAC[A/G]AGAAATGCAAAGTAT	10529
rs33962406	in-del	-/A	0.476052	0.106772	intron-variant	NEBL	GRCh38.p7	10:20800716	AGGTTGCGATATTTG[-/A]AAAAAAAAATCTACC	10529
rs34007668	in-del	-/T			intron-variant	NEBL	GRCh38.p7	10:21165637	CCCAATCTCGTCTAC[-/T]GTGCCAGGCTTGGGG	10529
rs34016284	in-del	-/C			intron-variant	NEBL	GRCh38.p7	10:20990919	ATCCTGCTTTTCTCC[-/C]TTCCCTTTCTTCCTG	10529
rs34018340	in-del	-/G			intron-variant	NEBL	GRCh38.p7	10:20985892	GAATGGGCCTACAGG[-/G]TGAGTTCAGATTTTT	10529
rs34028730	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:20830276	TCTGCATAAACTCCA[-/A]TTAATCAAATTAAAT	10529
rs34036235	in-del	-/A	0	0	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21144957	AAGCCCCTTCAAATT[-/A]AAAAAAAAAAAAAGA	10529
rs34045905	in-del	-/C			intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20961067	CAGGTGTGAATTACC[-/C]AAAACTTAGAAGAGC	10529
rs34049869	snp	C/T	0.375	0.216506	intron-variant	NEBL	GRCh38.p7	10:21079387	GGCAGGTGCTTTCAT[C/T]TAAACCTCCCAGCAC	10529
rs34054865	in-del	-/C			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21128685	GAAGACCAACAAGAG[-/C]AACATCATCAACACC	10529
rs34054881	in-del	-/T			intron-variant	NEBL	GRCh38.p7	10:21151529	AAAAACTTAAAACCT[-/T]AAATCACACATCACG	10529
rs34059594	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:20997726	TTATAATAGCTTCAG[G/T]GGTAATGTTCTGATC	10529
rs34064520	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:21047548	TTTTAAAAAAAAAAA[-/A]GATTTTTTTTAACAC	10529
rs34064580	snp	G/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20871394	TATTCATATATCTTG[G/T]TAGTTTCCTTTCAAT	10529
rs34075344	in-del	-/G			intron-variant	NEBL	GRCh38.p7	10:21023370	GGGCATGCTTTGGGG[-/G]AACAACCTTCTTCTG	10529
rs34118064	in-del	-/CA			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20867436	AGTATTTTCAAAGTC[-/CA]AAAAAAACTATAAAT	10529
rs34133056	in-del	-/A	0.417034	0.18601	intron-variant	NEBL	GRCh38.p7	10:20919970	TATCTAAAAATTGAG[-/A]AAAAAAATCAACAAC	10529
rs34139031	in-del	-/A/AA			intron-variant	NEBL	GRCh38.p7	10:20924524	AAAAAAAAAAAAAAA[-/A/AA]TCCCAGCAGGTAGCT	10529
rs34154647	in-del	-/C			intron-variant	NEBL	GRCh38.p7	10:20913605	AAAAACCAAGTGTAC[-/C]GAAATATCGTATCAG	10529
rs34159675	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:21019574	TGATGTGTTTCACCA[-/A]TATTGAAGGCAAGTT	10529
rs34160015	in-del	-/C			intron-variant	NEBL	GRCh38.p7	10:21089768	CTCCTTCCCCTGCCC[-/C]AGATAAACATCAAAT	10529
rs34186944	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:20803477	ATCTTGAACCAAAAA[-/A]TTTTAACTACATTTT	10529
rs34200837	in-del	-/C			intron-variant	NEBL	GRCh38.p7	10:20956249	AGAAATACTTTTCCC[-/C]GAGGAGCGGTTGTTC	10529
rs34205144	in-del	-/G	0.419616	0.183658	intron-variant	NEBL	GRCh38.p7	10:21162353	AATTATCAAATCTGA[-/G]GGGGGTCGTGGGAAC	10529
rs34205265	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21082246	GTACAAGGCATCATT[C/T]TAGATTGGATCCTTT	10529
rs34236522	in-del	-/T			intron-variant	NEBL	GRCh38.p7	10:20919233	AAATTATATACTTTT[-/T]AGAAAATTATGCAAC	10529
rs34245405	in-del	-/T			intron-variant	NEBL	GRCh38.p7	10:21026084	ACATGAAAAAGTTTT[-/T]ATAAATGGAAAACTA	10529
rs34273585	in-del	-/G			intron-variant	NEBL	GRCh38.p7	10:20974682	TTAACCTTTAATGGT[-/G]TACACATACTACCAA	10529
rs34275029	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21118665	TGTATTTAGACACTG[G/T]TTTAGATATGCCATG	10529
rs34284427	in-del	-/C			utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20784931	TTCAATAATAGGAAC[-/C]GCGCAGTGCAGCTGC	10529
rs34292255	in-del	-/T			intron-variant	NEBL	GRCh38.p7	10:21036717	ACGTTCCTCCAGCAG[-/T]AAGAGGCATCTACCC	10529
rs34295157	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:21086040	ACTTTGAAAAAAAAA[-/A]TCCATAAATATGTGT	10529
rs34347929	in-del	-/G			intron-variant	NEBL	GRCh38.p7	10:20789761	GAAGGCTGAGGTGGG[-/G]AGGATTGCTTGTATC	10529
rs34368396	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:20983339	CAGTGTACTGCAAAA[-/A]GTATGTGCTAAACTT	10529
rs34386607	in-del	-/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20852032	AAAAATAACGACTTT[-/T]AAAGTATGCTAGAGA	10529
rs34388336	in-del	-/G			intron-variant	NEBL	GRCh38.p7	10:21169260	TAAAAAGTGACAGGG[-/G]AAGACGAAGAGTTGT	10529
rs34393866	in-del	-/C			intron-variant	NEBL	GRCh38.p7	10:21163374	CAGTGCAGGTTATCC[-/C]AAACAGGCCATCAAA	10529
rs34410523	in-del	-/C			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20882239	AAAAAAGGAAGGAAG[-/C]GAAGGAAAAGGAAAA	10529
rs34413299	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:20986792	ACTTGAAAATGTAAA[-/A]TGAAATGAGACTGAC	10529
rs34415549	in-del	-/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20869974	CTTAAGTTGGCTTTT[-/T]GTGCATCTATTTGTA	10529
rs34426551	in-del	-/C			intron-variant, upstream-variant-2KB	NEBL, NEBL-AS1	GRCh38.p7	10:21173171	GAGGGGCCCGGCTAC[-/C]AGAACTACTTCCCCT	10529
rs34427653	in-del	-/G			intron-variant	NEBL	GRCh38.p7	10:20908270	TGCTAGGCCATAGGG[-/G]CAGTAGAACATTGAA	10529
rs34432407	in-del	-/C			intron-variant	NEBL	GRCh38.p7	10:21113693	AATGGAACTCCTCCC[-/C]TTTCCTTGGTTTTTA	10529
rs34433650	in-del	-/T			intron-variant	NEBL	GRCh38.p7	10:20842942	TTTTAGATTCCACAT[-/T]AAAAGTGAGAATATG	10529
rs34445606	in-del	-/G			intron-variant	NEBL	GRCh38.p7	10:20837520	CATCTCCATCATATG[-/G]AAAGTGCAAGGTGAA	10529
rs34445762	in-del	-/G			utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20785496	ATAGCCAATCAAAGG[-/G]AAACCATGAACACAA	10529
rs34470051	in-del	-/AT			intron-variant	NEBL	GRCh38.p7	10:21029942	CGTGCAGCTCCAGAG[-/AT]GATTTCTCTCGGGAT	10529
rs34473359	in-del	-/T			intron-variant	NEBL	GRCh38.p7	10:20957372	AGAGAGATTACTTTT[-/T]GGTATACTTTTTTAA	10529
rs34512601	in-del	-/C			intron-variant	NEBL	GRCh38.p7	10:21162137	ATTGGTGGAGATCCC[-/C]TGGTTGATGATTGCA	10529
rs34527446	in-del	-/C			intron-variant	NEBL	GRCh38.p7	10:20903157	ATATTATGTTTTTCC[-/C]TATACATACATACCT	10529
rs34533049	in-del	-/C			intron-variant	NEBL	GRCh38.p7	10:20976986	GGAACATAGCCAACC[-/C]AAAAACACTAGGCTT	10529
rs34539930	in-del	-/A			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20879195	GGTGGAGACAGCAAA[-/A]GTGGAACAGAAAGAG	10529
rs34556362	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20928361	TACCATGCTACACAG[A/C]TGAGTGCTAAGGTAA	10529
rs34566532	in-del	-/A	0.478437	0.10157	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21130122	TTCAAAACAGGGTAG[-/A]ACTTCAAAACAGGGA	10529
rs34595479	in-del	-/G			intron-variant	NEBL	GRCh38.p7	10:21168323	GCATATTCTTAATAT[-/G]TTATTTTAAAGGTTC	10529
rs34616036	in-del	-/C			intron-variant	NEBL	GRCh38.p7	10:21096100	TCCATTTATTTTCCC[-/C]TAAAGAGAAATGTAA	10529
rs34623754	snp	A/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20875090	GCTTCCAACGAATAT[A/T]TGAATTCCATCAAAA	10529
rs34636190	in-del	-/G			intron-variant	NEBL	GRCh38.p7	10:21150466	GGCTCCAACCACGGG[-/G]CTTGCACAACTACAA	10529
rs34636220	in-del	-/T			intron-variant	NEBL	GRCh38.p7	10:21078325	GAATGTATTCTTTTT[-/T]AAAGTAATAAGCCTT	10529
rs34663088	in-del	-/T			intron-variant	NEBL	GRCh38.p7	10:20972140	ACAGGATAAACCCAG[-/T]AATCAAGCAAATATA	10529
rs34672409	in-del	-/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20857690	GGGCAGTGCACCCAG[-/T]ATATTTTCATCAAGA	10529
rs34681227	in-del	-/C			intron-variant	NEBL	GRCh38.p7	10:21071548	GTACATTACAATCAC[-/C]TAGGACACTTTTAAA	10529
rs34685634	in-del	-/A/AA	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21010606	CCATTCAAAAAAAAA[-/A/AA]TAAGAAAGCATTAGG	10529
rs34695545	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:20834438	TGATCAGGAAACCTA[-/A]TACCATCTCCACTTC	10529
rs34699596	in-del	-/C			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21144475	CACGCCTGTAATCCC[-/C]AGCACTTTGGGAGGC	10529
rs34700082	in-del	-/A	0.19646	0.2442	intron-variant	NEBL	GRCh38.p7	10:21076112	TGGTACAGCTATTAC[-/A]AAAAAAAACTGTATA	10529
rs34701031	in-del	-/G			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21131765	ACCACAAAGTTTGGG[-/G]AAAAGGAATAAGGAG	10529
rs34710843	in-del	-/G			intron-variant	NEBL	GRCh38.p7	10:21061906	TTGCTGCACTTTAGG[-/G]TTAACATAAGCTATA	10529
rs34713711	in-del	-/A/AA/AAA			intron-variant	NEBL	GRCh38.p7	10:20952904	GTGAGACCCTGTCTC[-/A/AA/AAA]AAAAAAAAAAAAAAA	10529
rs34722144	in-del	-/G			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20871091	TGCAAAGTGTACAGT[-/G]CATGGACATTCTTAA	10529
rs34724538	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:20814310	CTATCTAGTCTGTAA[-/A]CCTGCGCAAGCCCGA	10529
rs34729529	in-del	-/ATATATATATATATA	0	0	intron-variant	NEBL	GRCh38.p7	10:21169068	AAAAAAAAAAAAAAA[-/ATATATATATATATA]TATATATATATATAT	10529
rs34733062	in-del	-/G			intron-variant	NEBL	GRCh38.p7	10:20977853	TCTTGCAATGCAAGG[-/G]AATACTAAATACAGC	10529
rs34739583	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:20986380	ATAATTAAGCCAAAA[-/A]TAATTCAGCAACTCT	10529
rs34771372	in-del	-/T			intron-variant	NEBL	GRCh38.p7	10:20952167	CGGGGCCAGGCGGGG[-/T]GGCTCACACCTATAA	10529
rs34777547	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20999370	GGGAGGGTAAGGTGG[A/G]AGGGTTGCTTGACCC	10529
rs34788823	in-del	-/C			utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20782973	GTATCAAACTGTTCC[-/C]TTGTGCTTCTGTCAG	10529
rs34801954	in-del	-/T			intron-variant	NEBL	GRCh38.p7	10:21095780	TTCCCTTCAGCTTTT[-/T]GAGAAAATGACAAGG	10529
rs34825490	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:21023300	AATGTGTTACAGAAA[-/A]GTTTAGCCCGTTGAG	10529
rs34836918	in-del	-/C			intron-variant	NEBL	GRCh38.p7	10:20841001	GCTTTTTTCCTACAG[-/C]ACACTTCATTTTCCC	10529
rs34851028	in-del	-/C			intron-variant	NEBL	GRCh38.p7	10:20834454	ACCATCTCCACTTCC[-/C]TTTGTCTTATTCAAT	10529
rs34867473	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21075131	TTTTTAAAAAGAAGA[A/C]CAATAACCAGAAAGA	10529
rs34875753	in-del	-/C			intron-variant	NEBL	GRCh38.p7	10:21097860	AATAGTCACAGCTCC[-/C]ATGAGAAAGACTCTA	10529
rs34885917	snp	A/G	0.0314385	0.121371	intron-variant	NEBL	GRCh38.p7	10:20916352	CTAGAGTTCTATTAC[A/G]AAATATTTCTTAGAT	10529
rs34924296	snp	A/C			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20860256	AGCATGACGTGTACC[A/C]CAGTTTTTCTCATCA	10529
rs34927229	in-del	-/G			intron-variant	NEBL	GRCh38.p7	10:20935475	CCCCCAAGAACATGC[-/G]TCCCCTCGGTAGTGA	10529
rs34933486	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21075137	AAAAGAAGAACAATA[A/C]CCAGAAAGAAGAAAG	10529
rs34947663	snp	G/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20854747	TTTCTTTATTTTTTG[G/T]GGAGCTAGGGTCCCA	10529
rs34949716	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:20826188	TTCAAAGAGATGAAA[-/A]TCTAACCCTAGGTTT	10529
rs34974239	in-del	-/AA			intron-variant	NEBL	GRCh38.p7	10:20976353	AAAAAAAAAAAAAAA[-/AA]GTTTGGAGATTTCTC	10529
rs35020371	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20969351	CATGTCCATAGATTT[C/T]TAAGCTTTCAATTAA	10529
rs35031266	in-del	-/ACAC	0.469148	0.120308	intron-variant	NEBL	GRCh38.p7	10:20963004	AAGCTTGAAAGAAAA[-/ACAC]ACACACACACACACA	10529
rs35034577	snp	C/T	0.0240643	0.107019	intron-variant	NEBL	GRCh38.p7	10:20926087	GCCTCTTATGAAATC[C/T]TATAGGCCATATAAA	10529
rs35042528	multinucleotide-polymorphism	AA/GG	0	0	intron-variant	NEBL	GRCh38.p7	10:20931284	TAAAAAAAAATCTTT[AA/GG]CACATCTTTAAACTG	10529
rs35046645	in-del	-/G			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20855584	AGAACTTCGAATGCG[-/G]TGTCTTTCCTTATAT	10529
rs35067415	in-del	-/A	0.479583	0.0989539	intron-variant	NEBL	GRCh38.p7	10:21027302	TAACGTATTATCTTT[-/A]AAAAAAAAACAACAA	10529
rs35075796	in-del	-/T			intron-variant	NEBL	GRCh38.p7	10:20815102	TGAAGCCCTGATATT[-/T]CACTAAGAGGAAGCA	10529
rs35104609	in-del	-/GA			intron-variant	NEBL	GRCh38.p7	10:20828782	AGAGAGAGAGAGAGA[-/GA]GGTGGAGAGACAGAG	10529
rs35120095	in-del	-/C			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21139300	AAGGTTTTGAAAGAA[-/C]AATGTAAAATCCAAT	10529
rs35126162	in-del	-/G			intron-variant	NEBL	GRCh38.p7	10:20900309	GCCATGTCCTCTAGG[-/G]CAAATTATTCAACCC	10529
rs35138083	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21044500	AACTGGTACACTTCA[A/G]AACATATCCTGAGAA	10529
rs35138107	in-del	-/A	0	0	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20870326	AAAAAAAAAAAAAAA[-/A]CTTGAACTGAATTTA	10529
rs35140193	in-del	-/G			intron-variant	NEBL	GRCh38.p7	10:21065219	GCCTTAGTTACAAGG[-/G]AATACAGCAGTCTTT	10529
rs35142286	in-del	-/A	0	0	intron-variant	NEBL	GRCh38.p7	10:20925714	AATTAAAAAAAAAAA[-/A]GGCAGAACAGAAGCT	10529
rs35149709	in-del	-/T			intron-variant	NEBL	GRCh38.p7	10:21038100	CAAAACTATGCCTTT[-/T]AAGGTTTTGAGGGCA	10529
rs35204600	in-del	-/G			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21128663	AGAGAACAAAAGCAA[-/G]AAAAAAGGAAGACCA	10529
rs35213426	in-del	-/GG	0.0486741	0.148216	intron-variant	NEBL	GRCh38.p7	10:20828766	TGACTTACACTCCCA[-/GG]GAGAGAGAGAGAGAG	10529
rs35228806	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20967339	AAAGCAAGAAATGTA[A/G]ACACAGGGCTGGGCA	10529
rs35250062	in-del	-/G			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20876904	AAAAACTGGCAGGGG[-/G]TATGTCCCTTAAGGT	10529
rs35253917	in-del	-/TG	0.475789	0.107327	intron-variant	NEBL	GRCh38.p7	10:21038497	TTAGTTTGCTAAGAC[-/TG]ATGGCTTACAGCTTC	10529
rs35255678	in-del	-/T			intron-variant	NEBL	GRCh38.p7	10:20800741	CTACCAATACTATTT[-/T]CTACATCATTAATCC	10529
rs35275601	in-del	-/C			intron-variant	NEBL	GRCh38.p7	10:20977871	ACTAAATACAGCCCC[-/C]GGTTTTATCTGTAAC	10529
rs35281592	in-del	-/ATAA			intron-variant	NEBL	GRCh38.p7	10:21037825	TGAAGAGTAGAAAGA[-/ATAA]TAGACAAAATGAGAG	10529
rs35293466	in-del	-/C			intron-variant	NEBL	GRCh38.p7	10:21091048	TCTCCTCCATGCCCC[-/C]AAGGTCAACTCCACC	10529
rs35311871	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:20834071	TTGCAGACAACAAAA[-/A]GATAAATGGTCACAT	10529
rs35312464	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:20975250	AAATAAGATCTTAAA[-/A]GTACTAGAAGTGGGA	10529
rs35313485	in-del	-/A	0.0162398	0.0886349	intron-variant	NEBL	GRCh38.p7	10:21093483	TCGGCACTGAAAAAA[-/A]TCCATCAGTGTTCAT	10529
rs35376055	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21082349	ATAAATATTAGTGTT[C/T]TGATTTGGATGGTTA	10529
rs35384674	in-del	-/G			intron-variant	NEBL	GRCh38.p7	10:20799949	TGTGTGTGTGTGTGT[-/G]AGACGGAGAAAGAGA	10529
rs35387771	in-del	-/T			utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20784188	TGCAGTTTTGCTTTT[-/T]CGGTTTTGTCATAGC	10529
rs35388534	in-del	-/AAC	0.499551	0.0149693	intron-variant	NEBL	GRCh38.p7	10:20904045	ATGTCATAGCAAGAG[-/AAC]AACTAGTAATAAAAT	10529
rs35397786	in-del	-/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20866222	TTCTGGGAAGGGGGC[-/T]GTTGGGGAGTTATTA	10529
rs35408978	in-del	-/G			intron-variant	NEBL	GRCh38.p7	10:21056817	TAAAAGAAAGCAAGG[-/G]AAATTATAACCACAA	10529
rs35412364	in-del	-/A	0.441043	0.161253	intron-variant	NEBL	GRCh38.p7	10:21067980	GATGCCGTCTCAAAG[-/A]AAAAAAAATGTAATA	10529
rs35413279	in-del	-/T			intron-variant	NEBL	GRCh38.p7	10:21027339	CAACAACTTTTTTTG[-/T]TTTTTTTTTTTTAAT	10529
rs35422327	snp	C/T	0.00318978	0.0398085	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20781754	TTGATCAACAGTTGA[C/T]AGTTAGTTGCGAGGA	10529
rs35424818	in-del	-/C			intron-variant	NEBL	GRCh38.p7	10:20932068	TCATTACAAACATTT[-/C]ATTCTTCAGCATGTT	10529
rs35436080	in-del	-/T			intron-variant	NEBL	GRCh38.p7	10:20989269	GTTTAAAAACATATT[-/T]AATCCAACTTTACTT	10529
rs35445738	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21066692	ACCATTGCTTAAAAC[A/C]CAGCAATACAAGAGA	10529
rs35454751	snp	A/C			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21143444	AAAGAGTGAAACTTC[A/C]TCTCAAAAAAAAAAA	10529
rs35474832	in-del	-/C			intron-variant	NEBL	GRCh38.p7	10:20820798	CCACTGCACTCCAGC[-/C]TGGGTGACAGAGTAA	10529
rs35479659	in-del	-/G			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20851500	TTGTGAAATGGCCGG[-/G]TGCAGTGGCTCACAC	10529
rs35507662	in-del	-/T	0.460702	0.134554	intron-variant	NEBL	GRCh38.p7	10:21103741	TCTCTGGCTCCCTAG[-/T]TCATGACATGCGATT	10529
rs35521478	in-del	-/G			intron-variant	NEBL	GRCh38.p7	10:20995828	TATTTCTGAGTGGGG[-/G]AAGGCCCGCTCTGAG	10529
rs35536129	in-del	-/T			intron-variant	NEBL	GRCh38.p7	10:20799948	GTGTGTGTGTGTGTG[-/T]GAGACGGAGAAAGAG	10529
rs35540567	in-del	-/T			intron-variant	NEBL	GRCh38.p7	10:21119267	TTCTTCCTAACTTTT[-/T]ATTTTGAAAAATTTC	10529
rs35544464	in-del	-/A	0.485596	0.0836329	intron-variant	NEBL	GRCh38.p7	10:20931117	TTCCTTTCCCATAAG[-/A]AAAAAAAAATAAACT	10529
rs35546213	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:20801661	ATACAAGAGATACTA[-/A]GATAAATGTTTGATG	10529
rs35551853	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21082040	GCCACCTGATAGGAT[A/C]CCATGAAAAGAACAT	10529
rs35564579	in-del	-/G			intron-variant	NEBL	GRCh38.p7	10:20920741	TTTGGAAAATCATGG[-/G]AAACTTTTATACAAT	10529
rs35574671	in-del	-/A	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21024516	CCAAAAAAAAAAAAA[-/A]GAAGGCTTAACTATT	10529
rs35575100	in-del	-/G			intron-variant	NEBL	GRCh38.p7	10:20795243	AAGTGAGAAAGAGGG[-/G]AAAGGTAAAGAAAAA	10529
rs35580647	in-del	-/T			intron-variant	NEBL	GRCh38.p7	10:20903465	AATATGAAGCTTTTT[-/T]AAAGAACTAAAAGTA	10529
rs35584123	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:20992793	TTTTTTTTTTTTTTT[A/T]TTGAGGCGGAGTCTC	10529
rs35588316	in-del	-/C			intron-variant	NEBL	GRCh38.p7	10:20930692	CCTTCTGCCTTGAGC[-/C]TAAATAGACGGCTTC	10529
rs35591590	in-del	-/T			intron-variant	NEBL	GRCh38.p7	10:20995384	TGCTTGGTCACCTTT[-/T]CGGTGCAGGACAATC	10529
rs35595108	in-del	-/T	0.0314385	0.121371	intron-variant	NEBL	GRCh38.p7	10:20886540	TCTTAAAAAAAGAAA[-/T]TCTGGGGAAAGAAGT	10529
rs35600698	in-del	-/G			intron-variant	NEBL	GRCh38.p7	10:21067955	GCACTCCAGCCTGGG[-/G]TGACAACAAGATGCC	10529
rs35606192	in-del	-/A			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21130691	ATTTTGAACTGAATG[-/A]AAAATGAAAATACAA	10529
rs35610875	in-del	-/A	0.499722	0.0117779	downstream-variant-500B	NEBL	GRCh38.p7	10:20779572	GCAGATTATATGAAG[-/A]AAAAAAAAAATCCCC	10529
rs35616178	snp	A/G			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21130692	ATTTTGAACTGAATG[A/G]AAATGAAAATACAAC	10529
rs35624079	in-del	-/A	0.463018	0.130857	intron-variant	NEBL	GRCh38.p7	10:21056412	AAAAGCTGGACCTGC[-/A]AAAAAAGATAGACTG	10529
rs35627113	in-del	-/T			intron-variant	NEBL	GRCh38.p7	10:20992766	TGCAACTACAAAGTC[-/T]TTTTTTTTTTTTTTT	10529
rs35635365	in-del	-/TT			intron-variant	NEBL	GRCh38.p7	10:21010433	AATTTTTTTTTTTTT[-/TT]GCAAGAACAGGGTTT	10529
rs35643559	in-del	-/C			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21145098	CACAACCATTAGATA[-/C]TTACTTTTCATCCAG	10529
rs35644345	in-del	-/T			intron-variant	NEBL	GRCh38.p7	10:20956762	ATAATTTTTACCTTT[-/T]CTCATATTTAAAAAA	10529
rs35658545	in-del	-/C			intron-variant	NEBL	GRCh38.p7	10:21122323	AGCCACCACGCCCAG[-/C]CCGGGATCTCTCCCA	10529
rs35676602	in-del	-/A			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21135448	TAAAAAAAAAAAAAA[-/A]TCTGGCAATGATGCT	10529
rs35681648	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:21048387	GATGGTTGCCACTCA[C/G]AAAATCTCCCGGGGC	10529
rs35690834	in-del	-/G			intron-variant, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20880123	TCCCAGCACTTTGGG[-/G]AGGTTGAGGCAGGTG	10529
rs35715474	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:20926137	CAGATGCACAAAAAA[-/A]TGGCTTGAGTCGCTA	10529
rs35717312	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21082310	AAACTTTAATGGGGT[C/T]TGAGGATTAGATCAC	10529
rs35721319	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:20804207	GAAGGAAAAAATTCA[C/G]AGAAAAGGGACAGAT	10529
rs35727161	in-del	-/C			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21136494	CCACCATGCCCAGCC[-/C]TTTTTACTTCTTATT	10529
rs35730966	in-del	-/C			intron-variant	NEBL	GRCh38.p7	10:21038457	TGAGTGAGAACATGC[-/C]AGTGTTTGGTTTTCT	10529
rs35740302	in-del	-/G			intron-variant	NEBL	GRCh38.p7	10:21104961	TAGTAAAATGCTTTT[-/G]CTACACCAATTAAGA	10529
rs35742813	in-del	-/G			intron-variant, upstream-variant-2KB	NEBL, NEBL-AS1	GRCh38.p7	10:21172100	ACGTTCTCAGTGGGG[-/G]AAGTTCAGCAGCTTC	10529
rs35747096	in-del	-/G			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20865506	TTTCTTAACCACTAG[-/G]ACCAAACCATACTGC	10529
rs35751532	in-del	-/T			intron-variant	NEBL	GRCh38.p7	10:20833281	CTAAAGAAAGTCACA[-/T]GGTCAAGCCCAGAGA	10529
rs35756166	in-del	-/T			intron-variant	NEBL	GRCh38.p7	10:21047970	GAACCTTCCCTTTTT[-/T]GTGGGGGTACACAGC	10529
rs35763710	in-del	-/G			intron-variant	NEBL	GRCh38.p7	10:21014259	TTCCAAAACACTGGG[-/G]ATTACAGGAGTGAGC	10529
rs35764221	in-del	-/C			intron-variant	NEBL	GRCh38.p7	10:20908184	GTCACTAGGATTTAG[-/C]ACTGATAACTTGCCC	10529
rs35775412	in-del	-/A	0.462034	0.132445	intron-variant	NEBL	GRCh38.p7	10:21035737	ATCCTTATTACCTTC[-/A]AAAATCATACACATT	10529
rs35779316	in-del	-/C			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21142380	ACAGGACACCACCCC[-/C]AGAAGTTCCAGATCA	10529
rs35809150	in-del	-/A	0.42574	0.177808	intron-variant	NEBL	GRCh38.p7	10:20798111	CCTGTTTCTAATTAC[-/A]AAAAAAAAAAAAAAA	10529
rs35829852	in-del	-/C			intron-variant	NEBL	GRCh38.p7	10:21164365	ATCTCTCTTACTCCC[-/C]TGATGTCCTAGGAAC	10529
rs35841488	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21165957	TTTCAATCACCACTT[C/T]CAATAAAAAATATTT	10529
rs35842534	in-del	-/C			intron-variant	NEBL	GRCh38.p7	10:20930678	TCCCACTTGCTACCC[-/C]TTCTGCCTTGAGCCT	10529
rs35844920	in-del	-/G			utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20780798	AGACCACTTGCAGGG[-/G]AACACATTAAAGCCA	10529
rs35856892	snp	A/G	0.35445	0.227135	intron-variant, upstream-variant-2KB	NEBL, NEBL-AS1	GRCh38.p7	10:21172303	TGACACAGTGAGTCA[A/G]TTCTTCAAAACAGGC	10529
rs35874521	in-del	-/C			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20849190	TTGTGTGTCTGATCC[-/C]TGAAAAGGTAAGAAG	10529
rs35877653	in-del	-/C			intron-variant	NEBL	GRCh38.p7	10:21108277	ACATTAGATCTTTCC[-/C]TTCTTTCTCTTGTGG	10529
rs35897508	in-del	-/C			intron-variant, downstream-variant-500B	NEBL	GRCh38.p7	10:20815433	ATCTGGAAATAACAA[-/C]AGAGTTGCAAAATAA	10529
rs35900455	in-del	-/A/AAA			intron-variant	NEBL	GRCh38.p7	10:21154474	AAAAAAAAAAAAAAA[-/A/AAA]GTGAGCCACAATGTA	10529
rs35903606	in-del	-/T			intron-variant	NEBL	GRCh38.p7	10:20801722	AACACCAGGGCAATT[-/T]GGCCGCACAGTTGAT	10529
rs35932109	in-del	-/CCTA	0.255	0.24995	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20865242	AAACTATTTTGAATA[-/CCTA]AAGTAAAATTATTCC	10529
rs35935078	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:20945682	ATGCAGATCCCAAAA[-/A]TGCCGTTTAAGAACA	10529
rs35937796	in-del	-/AA/AAA			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21141074	CAAAAAAAAAAAAAA[-/AA/AAA]CCTGCTCTATGCTCT	10529
rs35938506	in-del	-/A	0	0	intron-variant	NEBL	GRCh38.p7	10:20894751	AAAAAAAAAAAAAAA[-/A]TACAAAAAAATTAGC	10529
rs35943625	in-del	-/TT	0.195526	0.243993	intron-variant	NEBL	GRCh38.p7	10:20794333	GACTCTCATATTATC[-/TT]TGTTTTAATTTTCTA	10529
rs35961495	in-del	-/G			intron-variant	NEBL	GRCh38.p7	10:21063496	TAATGAAATCCATGG[-/G]AAACATGACAGAAAT	10529
rs35969284	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21082324	TCTGAGGATTAGATC[A/C]CAGTGATAAATAAAT	10529
rs35972559	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:20946763	GTATGTGTAATATAG[G/T]TCACAATCTAAAAGT	10529
rs35982918	in-del	-/G			intron-variant	NEBL	GRCh38.p7	10:21040471	TGAAGGGGGAGCAGG[-/G]TATGTTACCTGGTGA	10529
rs35992547	in-del	-/G			intron-variant	NEBL	GRCh38.p7	10:21061681	TTCAGAGACCCTGGG[-/G]AAAAAAGAAGCATGC	10529
rs35995810	snp	A/C/T	3.30006e-05	0.00406192	missense, upstream-variant-2KB	NEBL, NEBL-AS1	GRCh38.p7	10:21172419	TCATAGCCTTTGTAG[A/C/T]TGTTCATGTTGAGTG	10529
rs35998876	in-del	-/C			intron-variant	NEBL	GRCh38.p7	10:20999430	GCAAGACCCCATCCC[-/C]TACTAAAAATTTAAA	10529
rs36004930	multinucleotide-polymorphism	CA/TG			intron-variant	NEBL	GRCh38.p7	10:21038365	GTCTCTCCCCTTTAC[CA/TG]CCAGCCCCTGGCAGG	10529
rs36026113	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:21118134	CACTACCAATGAAAA[-/A]CTACAGCCTACACCT	10529
rs36029996	in-del	-/A/AAAAA			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20868067	AAAAAAAAAAAAAAA[-/A/AAAAA]CGCTGTTGGAGTCTA	10529
rs36031138	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21082192	AGCAACGAAGGAACT[C/T]TTGCAGGTTAGTGGA	10529
rs36034071	in-del	-/TT	0.498323	0.0289051	intron-variant	NEBL	GRCh38.p7	10:20887435	TTTTTTTTTTTTTTT[-/TT]GAGACAGAGGCTCAC	10529
rs36070477	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:20978988	AGGCATCAGTTAAAA[-/A]TTAAGTAAGTAAATA	10529
rs36108166	in-del	-/T	0.47666	0.105476	intron-variant	NEBL	GRCh38.p7	10:20926406	TATGTGAAATTTTGC[-/T]TCTTTTATGATCTCA	10529
rs36114108	in-del	-/T			intron-variant	NEBL	GRCh38.p7	10:20965715	TATCCTGCAAACTCC[-/T]TTGGAAGTGTGCAGG	10529
rs36115290	in-del	-/C			intron-variant	NEBL	GRCh38.p7	10:21015769	CTGCCACCTCAGCCT[-/C]CCCGAAGTGCTGGGA	10529
rs36157999	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20997405	GGGAAGGAAGTGGCC[A/C]CAGTCACCATTAGGT	10529
rs36183011	snp	A/C	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21044385	CTGGGTGACTGGATG[A/C]CAGAGTAAGAATAAA	10529
rs41277358	snp	A/G	0.00159617	0.0282053	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20780375	ATGATGCATTGTTGC[A/G]GTACTTTGATATAAA	10529
rs41277360	snp	A/G	0.00358779	0.0422022	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20782883	CTTACAACAAAAGCA[A/G]TATATTCTGTTGCTA	10529
rs41277362	snp	C/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20784027	AAAAGCATGTGCTAA[C/G]TTTTCTAAAGTGGAA	10529
rs41277364	snp	A/G	0.00014766	0.00859116	intron-variant	NEBL	GRCh38.p7	10:20787183	CAGCTAAGGAGGAAC[A/G]TATCAAATGGACACT	10529
rs41277366	snp	G/T	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:20823139	CATTTGACCTGTACA[G/T]GTTTTATGCTGTCAT	10529
rs41277368	snp	C/T	0.0858192	0.188533	intron-variant	NEBL	GRCh38.p7	10:20840659	AAAGTTATAGATGTA[C/T]AGAACCTTTGAGAAA	10529
rs41277370	snp	C/G	0.121904	0.214693	intron-variant, missense, nc-transcript-variant, upstream-variant-2KB	NEBL, LOC102725112	GRCh38.p7	10:20845353	TCTCCTTCTCAAAAT[C/G]CTCTTTGTAAACTTT	10529
rs41277372	snp	A/G	0.0236746	0.106192	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20852469	TCAGTTAAGACGCAC[A/G]GCAGTGAGCGGCGGG	10529
rs41277374	snp	C/G	0.00768213	0.0614984	intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20889923	ACACTTATCCTTGGA[C/G]TTTTTAAACTCTTCT	10529
rs41277376	snp	A/G/T	0.00572767	0.0532081	intron-variant	NEBL	GRCh38.p7	10:20889960	CGGATCTAAAAAAGA[A/G/T]AATGATTTACATAAG	10529
rs41307495	snp	C/G/T	0.00218505	0.0329819	missense, intron-variant, utr-variant-3-prime	C10orf113, NEBL	GRCh38.p7	10:21125835	CATTTACAAAAAAGT[C/G/T]ATTTTCAGCACCTTC	10529
rs41334046	snp	C/T	0.0260105	0.111035	intron-variant, upstream-variant-2KB	NEBL, LOC102725112	GRCh38.p7	10:20844176	CTAAAACCAGTTAAA[C/T]GGTATGACCAGTTAG	10529
rs45442995	snp	C/T	0.0189856	0.0955633	intron-variant	NEBL	GRCh38.p7	10:20948430	AAAATATTATTTTCT[C/T]CCTTAAGTAAATCAA	10529
rs45446496	snp	A/G	0.0166325	0.0896639	intron-variant	NEBL	GRCh38.p7	10:20954768	CAAGGCTCTACCCTA[A/G]TGGGCAGGCTGGTTG	10529
rs45447800	snp	C/G	0.0540123	0.155206	intron-variant	NEBL	GRCh38.p7	10:20983621	GATAACTAGCGCAGT[C/G]TAATTGTGTACAAGG	10529
rs45448294	snp	A/G	0.00755907	0.0610114	intron-variant	NEBL	GRCh38.p7	10:21118744	AAATTACATATGTGC[A/G]AAATGAGTCTTAATA	10529
rs45449796	snp	C/T	0.0103295	0.0711199	intron-variant	NEBL	GRCh38.p7	10:21002605	AGGCTGTACAGGAAG[C/T]ATGGATGGAGAGGTC	10529
rs45450201	snp	C/T	0.00597247	0.0543191	intron-variant	NEBL	GRCh38.p7	10:20995612	AGGACGCTGGAGAAA[C/T]GAAATGAACTCCCAA	10529
rs45452396	snp	C/T	0.0134861	0.0810011	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20854655	CTGCAGCCTTGACCT[C/T]CTGGGCTCAAGCAAT	10529
rs45454397	snp	G/T	0.00398564	0.0444627	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20780685	AAATGTGTAGAGATA[G/T]GAAATTAATGTGTTA	10529
rs45459693	snp	C/T	0.00478085	0.0486577	intron-variant	NEBL	GRCh38.p7	10:21097980	CGTGAAATGAACATT[C/T]GTAATAATCTCCTTT	10529
rs45461595	snp	C/T	6.59924e-05	0.00574385	intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20831487	CCTGGCTGGCCATCT[C/T]GGATGCTTTCTTAGC	10529
rs45463591	snp	G/T	0.0854556	0.188216	intron-variant	NEBL	GRCh38.p7	10:20826021	TGAACTGGTACTATT[G/T]GCCTTTTCAAATCTA	10529
rs45470096	snp	A/G	0.00597247	0.0543191	intron-variant	NEBL	GRCh38.p7	10:21091775	ATACTACAGATGCAC[A/G]CAACTACACAAGGCA	10529
rs45470794	snp	C/T	0.267091	0.249415	intron-variant	NEBL	GRCh38.p7	10:21003842	ATGAAAATCTCAAAA[C/T]GTATCTAAATTTCTT	10529
rs45471295	snp	C/T	0.0295035	0.117819	intron-variant	NEBL	GRCh38.p7	10:20950224	TCCTAGCAATGTGCG[C/T]GGCACATAGTAAACA	10529
rs45473194	snp	C/G	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:20937444	GTCACTTCAAAAGTT[C/G]AAAGAGCCAGGGGGT	10529
rs45480806	snp	A/C	0.0603597	0.1629	intron-variant	NEBL	GRCh38.p7	10:20963003	CAAGCTTGAAAGAAA[A/C]ACACACACACACACA	10529
rs45482791	in-del	-/ATC	0.18	0.24	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20898008	AAAATCATCATCATC[-/ATC]TTTGAATTCTGCAGT	10529
rs45489504	snp	A/C	0.0540123	0.155206	intron-variant, upstream-variant-2KB	NEBL, NEBL-AS1	GRCh38.p7	10:21172544	CAGGATGGGCACAGA[A/C]GGAAGGCTTTTTAGT	10529
rs45498799	snp	A/G	0.02016	0.0983543	intron-variant	NEBL	GRCh38.p7	10:20951877	AAATCTGCATCATGC[A/G]CTGGAAATTGAGACG	10529
rs45503098	snp	A/C	0.115788	0.21092	intron-variant	NEBL	GRCh38.p7	10:21018876	CTACTAAAAATACAA[A/C]AATTAGCCGGGTGTG	10529
rs45503797	in-del	-/AT	0.0512465	0.151648	intron-variant	NEBL	GRCh38.p7	10:20904655	TGTGCTTGTACATAT[-/AT]GTACATTCACACATG	10529
rs45505198	snp	A/G	0.0540123	0.155206	intron-variant, upstream-variant-2KB	NEBL, NEBL-AS1	GRCh38.p7	10:21172502	AAAAAAAAACATTTA[A/G]AAATACAGTACAATG	10529
rs45507192	snp	A/G	0.00478085	0.0486577	intron-variant	NEBL	GRCh38.p7	10:21015242	GAGGAGAGTCGGGGG[A/G]GTTTGGAGATGCCAG	10529
rs45513591	snp	A/C	0.0726307	0.176182	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20858682	TACAGTATTTCAACT[A/C]TGCTTTGTGGAGATC	10529
rs45515393	snp	C/T	0.119978	0.213528	intron-variant	NEBL	GRCh38.p7	10:20950792	TTCAATCACTTTGTT[C/T]ATGGGAAATTGATTC	10529
rs45516596	snp	C/T	0.137527	0.223271	intron-variant	NEBL	GRCh38.p7	10:20890316	CCTTGACACATAAGC[C/T]TTTGGCCAAACAGAA	10529
rs45516994	snp	A/G	0.00716266	0.059414	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20869314	AGAAACAGTTACGCC[A/G]TGTAGGAAGTGGACA	10529
rs45518036	snp	C/T	0.0115144	0.0749975	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20878939	AATTTCATTGAATTA[C/T]AGAGTTGGAAAGAGC	10529
rs45523038	in-del	-/CAGACCAAA	0.0512465	0.151648	intron-variant, downstream-variant-500B	NEBL	GRCh38.p7	10:20813633	TTTATGACAGGCAAA[-/CAGACCAAA]TTTTGTCTTAGAATT	10529
rs45525632	snp	G/T	0.161596	0.233848	intron-variant	NEBL	GRCh38.p7	10:21001922	TTTTTCCACCAACAC[G/T]TATTTCTCATTTGTG	10529
rs45526740	snp	C/T	0.00517822	0.0506191	intron-variant	NEBL	GRCh38.p7	10:20953878	TGCATTTATTGAGTA[C/T]GTGCTCTGTACTGAG	10529
rs45530234	snp	C/G	0.104938	0.20361	intron-variant	NEBL	GRCh38.p7	10:21159696	GTTTCCCTTCTTTTC[C/G]TTCTCACTCAAATGT	10529
rs45535836	snp	A/G	0.099723	0.199792	intron-variant	NEBL	GRCh38.p7	10:20995297	TTTCCAGTCCCTGGG[A/G]GTGGGGACAGCAGCT	10529
rs45541137	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21169809	CTCAGAATTCAACTT[A/G]AAACTAAAAATAATG	10529
rs45543632	snp	C/T	0.0182019	0.0936463	intron-variant	NEBL	GRCh38.p7	10:20786394	TCATAACATACTCAC[C/T]ATATAGGTTTCTGTA	10529
rs45544535	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20891596	TGACACATGCAGAAC[A/G]TTCAGGACAGGAGGA	10529
rs45546236	in-del	-/ACTC	0.39875	0.200931	frameshift-variant, intron-variant	C10orf113, NEBL	GRCh38.p7	10:21146413	TAGTAAAGCACAAAC[-/ACTC]TCTCTCATATAAGCT	10529
rs45547136	snp	C/T	0.0166325	0.0896639	intron-variant	NEBL	GRCh38.p7	10:20935594	CTGGAATCTGTGCCT[C/T]TTAATGAAATGGAAG	10529
rs45549131	snp	A/G	0.159951	0.233219	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20960030	GTTGGTAAAATGATC[A/G]GTATTTTTTAATTAA	10529
rs45551638	snp	A/G	0.00199481	0.0315187	intron-variant, downstream-variant-500B	NEBL	GRCh38.p7	10:20817350	CCAGTCTGGGTGACA[A/G]AGCAAGACCCTGTCT	10529
rs45553047	snp	C/T	0.00438332	0.0466095	intron-variant	NEBL	GRCh38.p7	10:21155963	ACTGATTATTGCCAC[C/T]GCTCAAAAGCAATAT	10529
rs45553737	snp	A/G	0.0573587	0.15934	intron-variant	NEBL	GRCh38.p7	10:21016480	GAAAATTTTTTAAAG[A/G]AAGAGATAACAGTGG	10529
rs45558231	in-del	-/CTTA	0	0	intron-variant	NEBL	GRCh38.p7	10:21066822	TTCTTACATTGTTCT[-/CTTA]GCGGTTTTTCTATTT	10529
rs45558639	snp	C/T	0.0444908	0.142359	intron-variant	NEBL	GRCh38.p7	10:20983894	TCCTATTTAAAATGC[C/T]TCAGGGAACTGGTAT	10529
rs45559637	snp	C/T	0.00517822	0.0506191	intron-variant	NEBL	GRCh38.p7	10:20926577	TCACATTCTATTCCT[C/T]AGGGGCATATTACTA	10529
rs45559734	snp	A/G	0.0023933	0.0345097	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20872318	ACAAGAGGACACCAC[A/G]GAGCCACACAGAAAA	10529
rs45560533	snp	G/T	0.0138799	0.0821421	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20782761	GGGCTACACTGCAAG[G/T]GTGTAAACAATAACA	10529
rs45561033	snp	C/T	0.02016	0.0983543	intron-variant	NEBL	GRCh38.p7	10:21088307	GGAGGTGGTGATCAG[C/T]CTGGGCAACATAGCA	10529
rs45562133	snp	G/T	0.124444	0.216185	intron-variant	NEBL	GRCh38.p7	10:21085145	CCTTCTAAACTCGCT[G/T]GATTTTCATGTGAGG	10529
rs45562145	snp	C/T	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:20949227	TGCATGTTCTCATTC[C/T]TAAGTGGGAGTCATA	10529
rs45564943	snp	G/T	0.110727	0.207612	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21138727	GTAACTTGCCCAGAG[G/T]CACACAGCTAAAAAA	10529
rs45567138	snp	G/T	0.158962	0.232835	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20959675	TGGTAATATTATGAA[G/T]TCTATATTTTTTACA	10529
rs45567340	snp	A/T	0.0267878	0.112589	intron-variant	NEBL	GRCh38.p7	10:20895469	TACTGAACCTCTCTG[A/T]GCCTCTATCTCCTCG	10529
rs45578138	snp	C/T	0.0689305	0.172377	intron-variant	NEBL	GRCh38.p7	10:20890664	GCTTAGCTAAACCTG[C/T]TCATCTCTTCTCTGC	10529
rs45578840	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21167525	TAATATAACTTGACA[A/T]TTGGTGAGAACACAT	10529
rs45581434	snp	C/T	0.0512465	0.151648	intron-variant	NEBL	GRCh38.p7	10:21122920	TCTCATCTTCCTAAG[C/T]TCTGTAGGATCAAGA	10529
rs45586437	snp	A/G	0.0543475	0.155628	intron-variant	NEBL	GRCh38.p7	10:20978034	AACACACATCCTTTT[A/G]AAAATCTTTTTTGTT	10529
rs45586536	snp	C/G	0.172028	0.23753	intron-variant	NEBL	GRCh38.p7	10:20905183	AAAACTAGATGATTT[C/G]GCACTTTTTGGAGAA	10529
rs45586736	snp	A/C	0.0479149	0.147179	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20859476	ATTTCCACTCTTGAA[A/C]AGATATAATAACTTC	10529
rs45586831	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21167231	CTGCTGTTTTATTTT[G/T]TAAAGTCTTCGGAAA	10529
rs45587543	snp	C/G	0.00597247	0.0543191	intron-variant	NEBL	GRCh38.p7	10:20977598	TGCCCAGATGAAAGG[C/G]TAATTCCACCAAATC	10529
rs45588131	snp	A/C	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20961184	AACTATATTAATAAA[A/C]AAGGCACAGCTTCAA	10529
rs45592638	snp	C/T	0.095	0.19615	intron-variant	NEBL	GRCh38.p7	10:20935556	CCTCCTTTGCAAGGA[C/T]ACTGTGCAATGAGAG	10529
rs45594837	snp	A/G	0.0524604	0.153226	intron-variant	NEBL	GRCh38.p7	10:20889128	TATGAAACACTAGAG[A/G]TCAGTCATTTACAAC	10529
rs45596338	snp	C/T	0.00557542	0.0525036	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21138720	AGGTTTGGTAACTTG[C/T]CCAGAGTCACACAGC	10529
rs45600533	snp	C/T	0.0512465	0.151648	intron-variant	NEBL	GRCh38.p7	10:21060055	AGTCCCTGTGACACT[C/T]TCTTCACTATGCTAG	10529
rs45601832	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21124613	ATGGGGAATGTAGAG[C/T]TTGGAAAAGAGCAAT	10529
rs45603138	snp	C/T	0.04875	0.148319	intron-variant	NEBL	GRCh38.p7	10:21101139	GCCACATGACTCAAG[C/T]CTCCCCTCTGTGTCA	10529
rs45603437	snp	G/T	0.00358779	0.0422022	intron-variant, upstream-variant-2KB	NEBL, LOC102725112	GRCh38.p7	10:20845067	TTCTCGCAACTTTAA[G/T]GGGAAATGTTAACAC	10529
rs45606741	snp	A/G	0.190833	0.242898	intron-variant	NEBL	GRCh38.p7	10:20954600	CTGGGTGAAAGGAAG[A/G]AAAGGGGGAAACAGG	10529
rs45607232	snp	C/G	0.0349115	0.127424	intron-variant	NEBL	GRCh38.p7	10:20994517	ACTCAAAGATAATTA[C/G]TTCCATTGGCCGTAA	10529
rs45612634	snp	C/T	0.00636936	0.0560724	intron-variant	NEBL	GRCh38.p7	10:20819954	ATTATTTATTGGTGG[C/T]CTCTCTGAGTTTGAT	10529
rs45616141	snp	C/T	0.191147	0.242974	intron-variant	NEBL	GRCh38.p7	10:21089858	TTTCCAAAAACATGT[C/T]CATAGTTCCAATATT	10529
rs45617835	snp	A/C	0.0512465	0.151648	intron-variant	NEBL	GRCh38.p7	10:21167163	AGTCAATAAATATTC[A/C]CGAGAGGGAATGTGA	10529
rs45628140	snp	A/C	0.00276761	0.0370964	intron-variant	NEBL	GRCh38.p7	10:20831592	AGTCTTTCTGCAGAA[A/C]ATGAAACATACAGTT	10529
rs55645433	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20792152	AGAAAGAAAGAAAAA[A/G]AAAAAGAAAAAAATG	10529
rs55647529	snp	A/G	0.402982	0.197728	intron-variant	NEBL	GRCh38.p7	10:21011462	AAACAGTCAGCTTAG[A/G]TCAATTCCCATTTCC	10529
rs55652844	snp	C/T	0.0962929	0.197165	intron-variant	NEBL	GRCh38.p7	10:20987881	ACTGACTCCACCTAC[C/T]GGAATTGCCCACCAG	10529
rs55687305	snp	A/G	0.390464	0.206809	intron-variant	NEBL	GRCh38.p7	10:21011744	CAGGAACAGCCTAGC[A/G]GTACCCCCTGAAGAC	10529
rs55712388	in-del	-/AAAAAAAAAAAAA			intron-variant	NEBL	GRCh38.p7	10:20997502	AAAAAAAAAAAAAAA[-/AAAAAAAAAAAAA]CAGAACTCCTGAAGA	10529
rs55713931	snp	A/T	0.0633504	0.166319	intron-variant	NEBL	GRCh38.p7	10:21165487	GCCTTCCCAAAAGAA[A/T]CTAGCCTGGGCCTTA	10529
rs55716025	snp	A/G	0.204803	0.245881	intron-variant	NEBL	GRCh38.p7	10:21114754	GCTGTATCTTTTTCC[A/G]TCCTTTAACTTTTAC	10529
rs55725603	snp	A/G	0.36606	0.221428	intron-variant	NEBL	GRCh38.p7	10:20829540	ATGTATACATATGTA[A/G]CTAACCTGCACATTG	10529
rs55763641	snp	A/T	0.296109	0.245711	intron-variant	NEBL	GRCh38.p7	10:20942008	TGTGAAAATGGCCAC[A/T]CTGCCCAAGGTAATT	10529
rs55772855	snp	C/T	0.0581099	0.160244	intron-variant, upstream-variant-2KB	NEBL, NEBL-AS1	GRCh38.p7	10:21173126	GCTGTTCATCTCCGT[C/T]CCTGCCCGGGAAGGG	10529
rs55778842	snp	C/T	0.364609	0.222182	intron-variant	NEBL	GRCh38.p7	10:20829558	AACCTGCACATTGTA[C/T]ACATGTACCCTGAAA	10529
rs55787617	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:21097264	AGGGGTTCGAGACCA[C/G]CCTGACCAACATTGT	10529
rs55814393	snp	C/T	0.117886	0.21224	intron-variant	NEBL	GRCh38.p7	10:20970049	CATATACAAAATATG[C/T]GTAATTTTAGTACAA	10529
rs55822856	in-del	-/A	0.242488	0.249887	intron-variant	NEBL	GRCh38.p7	10:21077222	TTTCTTCAAAAAAAA[-/A]TAAAAAATCAAAGGA	10529
rs55858607	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21043868	ATCTATTATAAAATT[A/T]AAAAAGTTGCCAATT	10529
rs55861136	snp	C/T	0.206336	0.246157	intron-variant	NEBL	GRCh38.p7	10:20903041	AATGATTCTTATCCA[C/T]AGAAATGCAAATTAT	10529
rs55883304	in-del	-/A			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21126997	AAAAAAAAAAAAAAA[-/A]CTCCACTGGCCAAAG	10529
rs55907432	snp	C/G	0.0115144	0.0749975	intron-variant	NEBL	GRCh38.p7	10:21169794	TCCTAGGGTGCTACC[C/G]TCAGAATTCAACTTA	10529
rs55931617	snp	A/G	0.172028	0.23753	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20960512	AAAGAGCAAAAAACA[A/G]TGTGTACTTTGCATC	10529
rs55938640	in-del	-/T			intron-variant	NEBL	GRCh38.p7	10:20910828	TGTTTTTTTTTTTTT[-/T]GGCCAAAGGGGGATA	10529
rs55945604	in-del	-/G/GAAGAAGAAGAAGAAGAAGAAGAAG/GAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAG			intron-variant	NEBL	GRCh38.p7	10:21028254	AAAAAAAAAAAAAAA[lengthTooLong]AAGAAGAAGAAGAAG	10529
rs55997015	snp	A/T	0.461703	0.132974	intron-variant	NEBL	GRCh38.p7	10:20803816	TCTGTACGAAAAATA[A/T]ATATATATATATATA	10529
rs56006104	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20792158	AAAGAAAAAGAAAAA[A/G]AAAAAAATGGTACTT	10529
rs56013237	in-del	-/AAA			intron-variant	NEBL	GRCh38.p7	10:21076472	AAAAAAAAAAAAAAA[-/AAA]GAATTACCACACAAC	10529
rs56014396	snp	C/T	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:20983189	AGTGAGAAAATCAAA[C/T]TAGATAATCTCCATA	10529
rs56029294	snp	A/T	0.275464	0.2487	intron-variant	NEBL	GRCh38.p7	10:20978446	AAAAAAAAAAACGAG[A/T]TATTTGATTAAATCA	10529
rs56070435	snp	A/G	0.399073	0.200692	intron-variant	NEBL	GRCh38.p7	10:21009775	CCCCCAGAGAATTCC[A/G]GTGGGAAGGTCCTTC	10529
rs56080635	in-del	-/TGGCATCTGT	0.318174	0.240525	intron-variant	NEBL	GRCh38.p7	10:21011685	ATCTGTTGGCATCTG[-/TGGCATCTGT]TGGCATCTGTTGGCA	10529
rs56097275	snp	A/G	0.0379877	0.132479	intron-variant	NEBL	GRCh38.p7	10:21026982	GAGCTTCACTGGTTG[A/G]CAGTGTTTGACATAG	10529
rs56106008	snp	A/G	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21047815	CTGTTAAAAGCAACC[A/G]GAATCTTCCCCGCAT	10529
rs56111406	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:20823181	ATACAATAAAATTTT[A/T]AAAAAATACTTAAGA	10529
rs56125221	snp	C/T	0.271162	0.249103	intron-variant	NEBL	GRCh38.p7	10:21044328	CTTGAACCCGGGAGG[C/T]GGAGGTTGAAGTGAG	10529
rs56131253	snp	C/T	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:20920480	AGGCAGATTTCTGCA[C/T]ACCGCTAAGGAGTCC	10529
rs56137796	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:20894950	AAAAAAAAAAAAAAA[-/A]TTAAGGCAGAATAAT	10529
rs56146667	snp	C/T			intron-variant, upstream-variant-2KB	NEBL, NEBL-AS1	GRCh38.p7	10:21172340	ACTGGCTCTCAAGCT[C/T]TGAGGCTGTGCCACA	10529
rs56167606	snp	C/T	0.0298908	0.118541	intron-variant	NEBL	GRCh38.p7	10:21150993	TTAATGACCACCACT[C/T]AGAAATATACAGATT	10529
rs56201636	snp	C/G	0.0111196	0.0737302	intron-variant	NEBL	GRCh38.p7	10:21156258	CATCTTTTTGGTGTG[C/G]TTGTAAGCACGGGGC	10529
rs56262080	snp	A/C	0.179425	0.239831	intron-variant	NEBL	GRCh38.p7	10:20978716	GCCGTGATTGTGCCA[A/C]TGCACTCCAGCCTGG	10529
rs56267980	snp	C/T	0.380529	0.213219	intron-variant	NEBL	GRCh38.p7	10:20829509	AGTTAGTGGGTGCAG[C/T]GCACCAGCATAGCAC	10529
rs56276562	in-del	-/GAGAA	0	0	intron-variant	NEBL	GRCh38.p7	10:21095336	AAGAAAAGCAGATAA[-/GAGAA]AAGATAAGACGAACA	10529
rs56293124	in-del	-/A	0.362523	0.223246	intron-variant	NEBL	GRCh38.p7	10:21024820	CTCCACCTCTCCAGC[-/A]AAAAAAGAAAAAGAA	10529
rs56325502	snp	C/T	0.0402882	0.136092	intron-variant	NEBL	GRCh38.p7	10:21094494	GAGACAGCGAGACTC[C/T]GTCTCAAAAAAAAAA	10529
rs56329139	snp	C/T	0.172028	0.23753	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20960513	AAGAGCAAAAAACAA[C/T]GTGTACTTTGCATCC	10529
rs56340002	snp	A/C	0.031825	0.122064	intron-variant	NEBL	GRCh38.p7	10:20892179	AGAGGACAAGCTGAT[A/C]TAAACCAGGCATGGT	10529
rs56343457	in-del	-/A/AA	0	0	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20860587	AAAAAAAAAAAAAAA[-/A/AA]CCTAGCTATTCACAT	10529
rs56352671	in-del	-/TTTT/TTTTT	0	0	intron-variant	NEBL	GRCh38.p7	10:21066990	TTTTTTTTTTTTTTT[-/TTTT/TTTTT]GAGACAGAGTCTTGC	10529
rs56366013	in-del	-/AAAAAAAA/AAAAAAAAAAA/AAGAAAAAAAAAAAAAAAAA			intron-variant	NEBL	GRCh38.p7	10:21113306	AAAAAAAAAAAAAAA[lengthTooLong]CCAGGAAAAAACTCC	10529
rs56366109	in-del	-/GAAGAAGAAGAAGAAGAAGAAGAAGAAGAAGAAG			intron-variant	NEBL	GRCh38.p7	10:21028252	AAAAAAAAAAAAAAA[lengthTooLong]AAAAGAAGAAGAAGA	10529
rs56408946	snp	A/G	0.34659	0.230587	intron-variant	NEBL	GRCh38.p7	10:21068468	ACCTTGGAGCTTTCA[A/G]TCAAACTATGGGGGG	10529
rs56409914	snp	A/G	0.0341408	0.126114	intron-variant	NEBL	GRCh38.p7	10:20983059	TAACCCTTGGGAACC[A/G]AAGAGGGGAGTATGG	10529
rs56412811	snp	A/G	0.0391387	0.134304	intron-variant	NEBL	GRCh38.p7	10:21095099	GTTTGTTTCCAATTC[A/G]CATTCCAAGGCCTCA	10529
rs56688407	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21081643	AGACGGTTGGTTTCC[A/C]AAGACTGTTCTTCAC	10529
rs56754569	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20787804	CATAACGTATGTTTA[A/G]CAACACGTTTGTTCG	10529
rs56764741	snp	C/T	0.136847	0.222927	intron-variant	NEBL	GRCh38.p7	10:21009487	TTTGTGTTGCCTTAA[C/T]TTCTGATTTAGCATC	10529
rs56782629	snp	A/C	0.0123036	0.0774623	intron-variant	NEBL	GRCh38.p7	10:21154105	AAAGGAACTTCTCAT[A/C]TTATTAATACCATAC	10529
rs56787413	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:20915608	TTTTATGGCTGCATA[C/G]TATTCCATGGTGTAT	10529
rs56790751	in-del	-/A	0.496968	0.0388195	intron-variant	NEBL	GRCh38.p7	10:20843548	AAAAGATTCTCCTTT[-/A]AAAAAATTAACATAA	10529
rs56797826	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20970591	GAGGTGAAGGCTGCA[A/G]TGAGCTGTGATCATG	10529
rs56821805	snp	C/G	0.0146672	0.084371	intron-variant	NEBL	GRCh38.p7	10:20931494	GTTCCTCTAAACTAA[C/G]AAAGATATGGGATGA	10529
rs56824304	snp	C/T	0.0494327	0.149241	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20783429	TTTGCTATGCAAACA[C/T]TATTACGTGAAGCTT	10529
rs56853312	snp	A/T	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21142834	TAATGCCTGAAGATC[A/T]GAGGTGGGACAGTGT	10529
rs56853452	snp	A/T	0.0792508	0.182605	intron-variant	NEBL	GRCh38.p7	10:20832612	AAGAAAAATGTTATT[A/T]AAAAAAACTATTAAC	10529
rs56861971	snp	C/T	0.167158	0.235875	upstream-variant-2KB, intron-variant	C10orf113, NEBL	GRCh38.p7	10:21147374	CTTTCTGGAATTCTT[C/T]TCTGACCCTGTTTCT	10529
rs56882453	in-del	-/CA			intron-variant	NEBL	GRCh38.p7	10:21125250	ACACACACACACACA[-/CA]GCCACTGTGCACATT	10529
rs56933922	snp	C/T	0.0372196	0.131242	intron-variant	NEBL	GRCh38.p7	10:20952046	ATAATTCAACCAAGA[C/T]CTGGAAAACTTAAAA	10529
rs56980548	in-del	-/TGTTTTT			intron-variant	NEBL	GRCh38.p7	10:20989304	AGGTTTTTTGTTTTT[-/TGTTTTT]GTTTTTGGAGGAAAT	10529
rs57019719	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20894959	AAAAAAATTAAGGCA[A/G]AATAATCATGTCCTA	10529
rs57043695	in-del	-/GTGTGTGTGTGT/TA			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20868341	TGTGTGTGTGTGTGT[-/GTGTGTGTGTGT/TA]AGGTTAAAACACAAT	10529
rs57087711	snp	A/C	0.0345262	0.126772	intron-variant	NEBL	GRCh38.p7	10:20794814	CTGCTTTTCAGGAAC[A/C]TCCTTAGTCTCGGGC	10529
rs57091318	snp	A/C	0.171057	0.237209	intron-variant	NEBL	GRCh38.p7	10:21163188	GTGAAAGGCTCTGAA[A/C]GTCTGCTAGAAACCC	10529
rs57099882	snp	C/T	0.0221141	0.102801	intron-variant	NEBL	GRCh38.p7	10:20914880	TTTTGTTTTTTGAGG[C/T]GGAGTCTCACTCTGT	10529
rs57149647	in-del	-/TT			intron-variant	NEBL	GRCh38.p7	10:21039085	TTTTTTTTTTTTTTT[-/TT]GTAAATTTGTTTAAG	10529
rs57155418	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20793545	GGTGTCTTATTTTTC[C/T]TTCTTTCTTTTCTTT	10529
rs57174011	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20793814	ATCCACCTTGGCCTC[A/C]CAAAATGCTGGGATT	10529
rs57176129	in-del	-/AAA	0	0	intron-variant	NEBL	GRCh38.p7	10:21044427	AAAAAAAAAAAAAAA[-/AAA]GCTCCTAACTGCAAG	10529
rs57182022	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21171342	TTCTGTCTCAAAAAA[A/T]AAAAAAAGAAAAAAA	10529
rs57183869	snp	C/T	0.0267878	0.112589	intron-variant	NEBL	GRCh38.p7	10:21060512	TTGCCTACTCAAAGA[C/T]ATCACTCTACAAACT	10529
rs57204715	snp	G/T	0.0260105	0.111035	intron-variant	NEBL	GRCh38.p7	10:20908648	TTAAGAAATAAATTT[G/T]TAATTAAAAAACAAT	10529
rs57233495	snp	A/T	0.2768	0.248559	intron-variant	NEBL	GRCh38.p7	10:20976923	TCCTGAATCTACATT[A/T]AAAAAAAAAAAAAAA	10529
rs57286177	snp	A/G	0.0678174	0.1712	intron-variant	NEBL	GRCh38.p7	10:21007767	AGCCTCTTGAATTAC[A/G]TCTGTGCTTGTTATA	10529
rs57289458	in-del	-/ATATATAT/ATATATATAT	0	0	intron-variant	NEBL	GRCh38.p7	10:20896517	TATATATATATATAT[-/ATATATAT/ATATATATAT]GCATTTTCCTGTTCT	10529
rs57298100	snp	A/C	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20943569	TGTTGTGCACATGTA[A/C]CCTAAAAGTTAAAGT	10529
rs57356285	snp	A/G	0.0611083	0.163768	intron-variant	NEBL	GRCh38.p7	10:21082602	GGAATAAATGGTCCA[A/G]CTCAGCAATGGGCTA	10529
rs57399126	in-del	-/GT			intron-variant	NEBL	GRCh38.p7	10:21096527	TGTGTGTGTGTGTGT[-/GT]TTTGAGACAGGGTCT	10529
rs57427509	in-del	-/AA			intron-variant	NEBL	GRCh38.p7	10:20825675	CTCAAAAAAAAAAAA[-/AA]GAAACTCAATGTACT	10529
rs57452633	in-del	-/AT			intron-variant	NEBL	GRCh38.p7	10:20929278	TATATATATATATAT[-/AT]TCCTATCACTGATTA	10529
rs57472807	snp	C/T	0.362313	0.223351	intron-variant	NEBL	GRCh38.p7	10:20988314	AAAACCCTTTCCACA[C/T]TACTCTGCCTCCTCA	10529
rs57485525	snp	A/T	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21166261	GAAAAGAAAAAAAAA[A/T]TTTCTACATCATGAT	10529
rs57536382	snp	C/G	0.0603597	0.1629	intron-variant	NEBL	GRCh38.p7	10:20937283	TTTATTTAACAGCAA[C/G]TTTCTTCTGAGTCAC	10529
rs57560890	snp	A/G	0.0228947	0.104514	intron-variant	NEBL	GRCh38.p7	10:20912664	ATTTCAGCATTTCCT[A/G]CTTACGTTGCACCTA	10529
rs57587942	in-del	-/G	0.00557542	0.0525036	intron-variant	NEBL	GRCh38.p7	10:20941937	CTCAATGAAATAAAA[-/G]AGGATACAAACAAAT	10529
rs57700147	in-del	-/AATAAT	0	0	intron-variant	NEBL	GRCh38.p7	10:21092624	AATAATAATAATAAT[-/AATAAT]GGCTCACCACCAGAG	10529
rs57738141	snp	A/C	0.077417	0.180873	intron-variant	NEBL	GRCh38.p7	10:20895042	TATGCCTATCTGTTT[A/C]ATTTTACCTACGTGG	10529
rs57773122	snp	A/G	0.115438	0.210697	intron-variant	NEBL	GRCh38.p7	10:20836334	TTCAAGCGATTCTCC[A/G]GCCTCAGCCTCCCGA	10529
rs57789027	in-del	-/T	0.190205	0.242744	intron-variant	NEBL	GRCh38.p7	10:21153329	AATTAATTTTTTTTT[-/T]AAGATGGAGTTTTGC	10529
rs57844177	in-del	-/AAA			intron-variant	NEBL	GRCh38.p7	10:20796392	AAAAAAAAAAAAAAA[-/AAA]CTTCTCTAAAATATT	10529
rs57918610	in-del	-/A	0	0	intron-variant	NEBL	GRCh38.p7	10:20888223	TGGGGGAAAAAAAAA[-/A]CAGGAAAAAAATAAA	10529
rs57959816	snp	C/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21000688	GCAAACAGAAATAAG[C/G]CTCCCAAAACGAGAA	10529
rs58005377	snp	C/T	0.00638864	0.0561561	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20858214	GCCACAAGGCAACTA[C/T]GGTTGCCGCTAGATG	10529
rs58009474	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:21160878	GGAAAAAAAAAAAAA[-/A]CATGATATGCAAGTA	10529
rs58019523	snp	A/C	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21168225	TCCATTAAAGAATGC[A/C]CTCAGGTAGCGATTA	10529
rs58040209	snp	A/G	0.122758	0.215196	intron-variant	NEBL	GRCh38.p7	10:21165267	TTAGAAAGATGTCAC[A/G]TTTTGAAACCAGACC	10529
rs58052801	snp	A/T	0.030665	0.119967	intron-variant	NEBL	GRCh38.p7	10:21115011	CTTTTTAATTAAGTG[A/T]TTTTTATGATTCCTT	10529
rs58058853	snp	C/G	0.136506	0.222754	intron-variant	NEBL	GRCh38.p7	10:20799538	CAAATGTAAACACAA[C/G]AGCATTTTTGGGACA	10529
rs58062029	snp	C/T	0.00478085	0.0486577	intron-variant	NEBL	GRCh38.p7	10:20954841	TAGCCTCTGAGCCAG[C/T]GTGGATGGGGAGAGG	10529
rs58068430	snp	A/T	0.0150606	0.0854603	intron-variant	NEBL	GRCh38.p7	10:20935555	TCCTCCTTTGCAAGG[A/T]TACTGTGCAATGAGA	10529
rs58080530	snp	C/T	0.0707826	0.174302	intron-variant	NEBL	GRCh38.p7	10:20973260	TTCTTTTTTTTTTTT[C/T]TTAAGAGACAGAGTA	10529
rs58113651	snp	A/C	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20978917	GCACAGTGAAATCTG[A/C]AATCTAAATGTCTCA	10529
rs58156548	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20807023	AAATCAGTGACCCCA[C/T]GTCCAAAAAAAGTAA	10529
rs58157498	snp	C/T	0.200182	0.244986	intron-variant	NEBL	GRCh38.p7	10:21044171	GGAGGCCAAGGCGGG[C/T]GGATCACCTGAGGTC	10529
rs58201221	snp	A/G	0.0425829	0.139564	intron-variant	NEBL	GRCh38.p7	10:21004421	CAAATATTAACAAGC[A/G]TAAATAAGAATCACC	10529
rs58214792	snp	C/T	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:20980445	ACACTGAAAGAAAAG[C/T]AGAGAAGAAAGAAAA	10529
rs58215047	snp	A/G	0.116838	0.211584	intron-variant	NEBL	GRCh38.p7	10:20804686	GGGGGAAGCATTCTT[A/G]GAAAGTTTGAGTAAA	10529
rs58238335	snp	A/C	0.0524604	0.153226	intron-variant	NEBL	GRCh38.p7	10:21171356	AAAAAAAAAGAAAAA[A/C]AAAAAAGAAAGAAAG	10529
rs58241639	in-del	-/GTGTGTGT			intron-variant	NEBL	GRCh38.p7	10:21096528	TGTGTGTGTGTGTGT[-/GTGTGTGT]TTTGAGACAGGGTCT	10529
rs58260079	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20935360	ACTGTGAGCCTACAA[C/G]TGACGCTAATATCAA	10529
rs58275105	snp	A/G	0.276267	0.248616	intron-variant	NEBL	GRCh38.p7	10:20978458	GAGTTATTTGATTAA[A/G]TCAAAAATTTAGAAA	10529
rs58275699	in-del	-/A	0.430136	0.173352	intron-variant	NEBL	GRCh38.p7	10:21166064	TAAAAATACAAAAAA[-/A]TTAGCCGGGCCTGGT	10529
rs58290483	snp	A/G	0.0770498	0.180522	intron-variant	NEBL	GRCh38.p7	10:21162872	CACTCCAATGCCAGA[A/G]GGCATAAGAACAGCA	10529
rs58384368	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21085091	CCACCAACCAATACC[A/G]CTTGGAAGACAAACC	10529
rs58401847	snp	C/T	0.357877	0.225527	intron-variant	NEBL	GRCh38.p7	10:20946791	AGTGGGGTAGAGTCT[C/T]AATATCAGGAGGCTG	10529
rs58448284	snp	G/T	0.277067	0.24853	intron-variant	NEBL	GRCh38.p7	10:21007042	GGAAAAGAGTCACTT[G/T]GGGGTTTCTTTCAAA	10529
rs58474800	snp	C/T	0.101301	0.200969	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20877029	AAACATTTCTTAACA[C/T]AAATTTCACATTGAT	10529
rs58488328	snp	G/T	0.123798	0.215808	intron-variant	NEBL	GRCh38.p7	10:20909574	TTAAAACTTAAAATT[G/T]TCTTTAAGTAGGATC	10529
rs58509168	snp	A/G	0.0193772	0.0965046	intron-variant	NEBL	GRCh38.p7	10:21104847	ACCATCAAGTAAGAC[A/G]TTAGCTTTACATTTT	10529
rs58537154	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:20805866	TCAAAAAAAAAAAAA[-/A]GTCAACTTTTTCTTA	10529
rs58547343	in-del	-/TTTA			intron-variant	NEBL	GRCh38.p7	10:21120424	ATATATATATATATA[-/TTTA]AATTTGATCACTGGT	10529
rs58569619	snp	A/G	0.248471	0.249995	intron-variant	NEBL	GRCh38.p7	10:20990369	AAGGTGATGGCCTTC[A/G]GGAGGTAATTAGATC	10529
rs58576465	snp	C/T	0.360632	0.224189	intron-variant	NEBL	GRCh38.p7	10:20988081	ATCCTCAAATACTCT[C/T]CCCTTCTGCTGTCTG	10529
rs58660607	snp	G/T	0.181978	0.240568	intron-variant	NEBL	GRCh38.p7	10:21105648	ACTGCAGTAAACATA[G/T]GTGTGCATGTGTCTT	10529
rs58849551	snp	C/T	0.0482946	0.147699	intron-variant	NEBL	GRCh38.p7	10:21109652	TTTTGTTTGGTAGGC[C/T]ATTAATTACTGCCTC	10529
rs58854201	snp	C/G	0.0123036	0.0774623	intron-variant	NEBL	GRCh38.p7	10:21108947	TGTCATCTGCAAACA[C/G]AGACAATTTGACTTC	10529
rs58854250	in-del	-/CTTTT			intron-variant	NEBL	GRCh38.p7	10:21105199	ATTTCTTTTTCTTTT[-/CTTTT]ATATTTTAAGTTCGG	10529
rs58878956	in-del	-/AT	0.478603	0.101197	intron-variant	NEBL	GRCh38.p7	10:20921794	CACACACACACATAT[-/AT]GTATACACACATGCA	10529
rs58937756	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20981414	ATCTCATAAAAAAAA[A/C]ACACACAAAATTATA	10529
rs59021345	snp	C/T	0.0197687	0.0974348	intron-variant	NEBL	GRCh38.p7	10:20993560	TCTGCTCCACATGTC[C/T]CCACACCCTGCTAGA	10529
rs59024329	in-del	-/AG	0.116838	0.211584	intron-variant	NEBL	GRCh38.p7	10:20799966	GACGGAGAAAGAGAG[-/AG]CGCACGCGTGTGAGA	10529
rs59118016	in-del	-/A			intron-variant, upstream-variant-2KB	NEBL, LOC102725112	GRCh38.p7	10:20844525	CATAAAAAAAAAAAA[-/A]GCTTTTAAAGGTGGA	10529
rs59128414	in-del	-/AC/ACACACAC			intron-variant	NEBL	GRCh38.p7	10:20963047	CACACACACACACAC[-/AC/ACACACAC]GGAAATCTAGATACT	10529
rs59153800	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21112478	ATCATTCTAAGCAAA[C/T]TATCACAAGGACAGA	10529
rs59197119	in-del	-/GTGT			intron-variant	NEBL	GRCh38.p7	10:21096489	GCAACTTGGTTTTGA[-/GTGT]GTGTGTGTGTGTGTG	10529
rs59225360	snp	C/T	0.135143	0.222054	intron-variant	NEBL	GRCh38.p7	10:21105256	TGTTACATAGGTATA[C/T]ATGTGCCATGTTTGT	10529
rs59247787	snp	C/T	0.113685	0.209567	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20846455	CTCACTTAGCACATG[C/T]GTTCCATACAGCAAT	10529
rs59257677	in-del	-/AA			intron-variant	NEBL	GRCh38.p7	10:21171362	AAGAAAAAAAAAAAA[-/AA]GAAAGAAAGGAAAAG	10529
rs59267074	snp	C/T	0.188946	0.24243	intron-variant	NEBL	GRCh38.p7	10:21102925	GCTGTACCTATCAAC[C/T]CATCACCTAGGTATT	10529
rs59275380	in-del	-/AA			intron-variant	NEBL	GRCh38.p7	10:20796393	AAAAAAAAAAAAAAA[-/AA]CTTCTCTAAAATATT	10529
rs59276470	snp	G/T	0.0119091	0.0762411	intron-variant	NEBL	GRCh38.p7	10:21097227	GGAGGTCCGGGGGGG[G/T]GGTGGGGCAGATCAC	10529
rs59284447	in-del	-/AC/TA	0.253404	0.249977	intron-variant	NEBL	GRCh38.p7	10:21125227	TGCACACATGCATAT[-/AC/TA]ACACACACACACACA	10529
rs59308558	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:20909006	GGCACTCTTTTTTTT[A/T]ATTTTTAATTTTTTG	10529
rs59361250	snp	C/T	0.00914312	0.0669923	intron-variant	NEBL	GRCh38.p7	10:20914242	AATGCTGGGTAAATT[C/T]GGGTGGGTCGCTATT	10529
rs59373848	snp	C/T	0.0543475	0.155628	intron-variant	NEBL	GRCh38.p7	10:20828004	GCGTGACAAAATAAT[C/T]GTACAACAAACCCCT	10529
rs59375122	in-del	-/T			intron-variant	NEBL	GRCh38.p7	10:21087482	TCTCTCCTCTTTTTT[-/T]CAGACTTTCTCTTCT	10529
rs59440829	in-del	-/ACACACAC			intron-variant	NEBL	GRCh38.p7	10:20963040	CACACACACACACAC[-/ACACACAC]GGAAATCTAGATACT	10529
rs59527608	in-del	-/TA			intron-variant	NEBL	GRCh38.p7	10:21051870	TTAAGTATTTAATTT[-/TA]AACTGAAAACTTCAC	10529
rs59528207	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20793558	TCTTTCTTTCTTTTC[C/T]TTTTTTTTTTTTTAA	10529
rs59559502	snp	C/T	0.0287284	0.116357	intron-variant	NEBL	GRCh38.p7	10:21116980	CCCAACCTGAATGAC[C/T]GGTAATTTTTATTGG	10529
rs59565983	snp	A/C/T	0.0275645	0.114116	intron-variant	NEBL	GRCh38.p7	10:20804654	AGGCTGGGGGAACAG[A/C/T]GTGTGCAAAAGCCCT	10529
rs59609079	in-del	-/A/AA	0	0	intron-variant	NEBL	GRCh38.p7	10:20952925	AAAAAAAAAAAAAAA[-/A/AA]GAAAAAGAAAAAAGA	10529
rs59636166	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:20793539	CATAATGGTGTCTTA[A/T]TTTTCTTTCTTTCTT	10529
rs59676170	snp	A/G	0.195526	0.243993	intron-variant	NEBL	GRCh38.p7	10:20895484	TGCCTCTATCTCCTC[A/G]CTTCAGAAATGAGAA	10529
rs59694641	snp	C/T	0.030278	0.119257	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21129009	GTGTGTGGTTCCACA[C/T]GTAAGCAGTTTGGAA	10529
rs59738464	snp	G/T	0.148661	0.22854	intron-variant	NEBL	GRCh38.p7	10:21154032	CTGATTCAGTGTTTT[G/T]GGGAAACTGTTTCCT	10529
rs59793024	snp	C/T	0.0486741	0.148216	intron-variant	NEBL	GRCh38.p7	10:21109896	GATTCTTCTCTCTTA[C/T]CTTCTTTACTAGTCC	10529
rs59817688	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:21044427	AAAAAAAAAAAAAAA[-/A]GCTCCTAACTGCAAG	10529
rs59843794	snp	C/T	0.206336	0.246157	intron-variant	NEBL	GRCh38.p7	10:20902141	GGGCGCGGTGGCTCA[C/T]GCTTGTAATCCCAGC	10529
rs59879931	snp	C/T	0.0441095	0.141807	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20899024	CAAGCATGCTGAACT[C/T]GGAAACCACAACTCT	10529
rs59891843	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20935121	AAGAACCACAGTCTA[C/T]CTGGCTAGAAAGAGA	10529
rs59914326	in-del	-/A			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21126997	AAAAAAAAAAAAAAA[-/A]CTCCACTGGCCAAAG	10529
rs59942130	in-del	-/T			intron-variant	NEBL	GRCh38.p7	10:20909260	ATTTTTTTTTTTTTT[-/T]ACCCTTTAACAGTTC	10529
rs59952920	snp	C/T	0.0349115	0.127424	intron-variant	NEBL	GRCh38.p7	10:20942434	ACCTTATACAAAAAT[C/T]AATTCAAGATGGATT	10529
rs60063476	snp	A/G	0.105924	0.204309	intron-variant	NEBL	GRCh38.p7	10:20788235	GGGTATTTTCGTAGC[A/G]TGCCCTTCATTGTCT	10529
rs60137449	snp	G/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20790537	ACCCAGGAGGAGGAG[G/T]TTGCAATGAACCGAG	10529
rs60149599	snp	C/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20936687	CTGAATCTAAATAAA[C/T]AATGCAGTGTTTTCT	10529
rs60174274	in-del	-/AACT	0.162253	0.234095	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20848621	ACCCTATTATGAACT[-/AACT]GTGCATGCAAGGGAT	10529
rs60213612	in-del	-/A			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21138839	AAAAAAAAAAAAAAA[-/A]GATTAATGGGACAGA	10529
rs60226954	snp	C/T	0.402982	0.197728	intron-variant	NEBL	GRCh38.p7	10:20992455	CACCATGCAGAATTC[C/T]TCTTTTGAGTGACGA	10529
rs60270033	in-del	-/A	0.21695	0.247806	intron-variant	NEBL	GRCh38.p7	10:20984125	CCTGAAAAAAAAAAA[-/A]GCTCCAAACTTCTAA	10529
rs60280860	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:20978755	CAAAAAAAAAAAAAA[-/A]GTTTGGAAAGGTGTG	10529
rs60300897	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:20969470	GGGGTTCTTTTACTT[-/A]AAAAAAAAAAAATGA	10529
rs60333655	snp	A/G	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:21103510	GAGCCACCGCACCAG[A/G]CCTTTTTCAACTCTT	10529
rs60365283	snp	C/T	0.186421	0.24178	intron-variant	NEBL	GRCh38.p7	10:21109436	TCGCATCAATGTTCA[C/T]CAGGGATACTGGCCT	10529
rs60375467	snp	C/T	0.356597	0.226135	intron-variant	NEBL	GRCh38.p7	10:20979860	TACAAGCACATGCCA[C/T]CATGGTCATCTAATT	10529
rs60416925	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21050470	TTGCCTCTAAATGGC[C/T]TTCCCTCTCCACATT	10529
rs60474131	in-del	-/TT			intron-variant	NEBL	GRCh38.p7	10:20794334	ACTCTCATATTATCT[-/TT]GTTTTAATTTTCTAG	10529
rs60554170	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:20902407	CAAAGACACTGTCTC[-/A]AAAAAAAAAAAATTT	10529
rs60557755	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:21051879	TAATTTAACTGAAAA[-/A]CTTCACCTATGAGGG	10529
rs60625264	snp	A/G			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20856756	CCTGTTCAATAGCCT[A/G]GGAACATTAATGTAC	10529
rs60656950	in-del	-/AA			intron-variant	NEBL	GRCh38.p7	10:20919976	AAAATTGAGAAAAAA[-/AA]TCAACAACCCAATAT	10529
rs60657589	snp	G/T	0.093777	0.195178	intron-variant	NEBL	GRCh38.p7	10:20944317	AAGCAGGAGAATCAC[G/T]TGAACCTGGGAGGCG	10529
rs60695829	snp	A/G	0.0298908	0.118541	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21142917	AAACCTGTCCCTGGT[A/G]CCAAAAAGGTTGGGG	10529
rs60755026	in-del	-/G	0.349671	0.229272	intron-variant	NEBL	GRCh38.p7	10:21149327	ACAGAGTCTGTCTCT[-/G]TCACCCAAGCTGGAG	10529
rs60757944	snp	A/G	0.0240643	0.107019	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20856682	AGCCAGCATGATGTA[A/G]GTGTCCTGGAACTGA	10529
rs60806384	in-del	-/AA			intron-variant	NEBL	GRCh38.p7	10:20894949	AAAAAAAAAAAAAAA[-/AA]TTAAGGCAGAATAAT	10529
rs60861134	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:21090201	TATTTATCACCCCAA[-/A]GAACCACTGCCTACT	10529
rs60881269	in-del	-/T	0.232943	0.249417	intron-variant	NEBL	GRCh38.p7	10:21071809	ACAATAGTGTTGGGC[-/T]TTTTGTTTTTGATTT	10529
rs60902235	in-del	-/AATAATAAT			intron-variant	NEBL	GRCh38.p7	10:21092621	AATAATAATAATAAT[-/AATAATAAT]GGCTCACCACCAGAG	10529
rs60905445	snp	A/C	0.341235	0.232758	intron-variant	NEBL	GRCh38.p7	10:20990625	TCTTGTTGTAACAAC[A/C]CAAACTAAGACACTT	10529
rs60953894	snp	A/G	0.0387552	0.1337	intron-variant	NEBL	GRCh38.p7	10:20928574	AAGCAGAAGCAATCC[A/G]TTGTGGGTGTCTCAC	10529
rs61000049	snp	C/G	0.089084	0.191327	intron-variant	NEBL	GRCh38.p7	10:20970482	TGTCTCTGCTCCCCC[C/G]ACCAAAAAAAAAAAT	10529
rs61057597	snp	C/G	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:20988807	TTGGCAAAGCCACCA[C/G]TGAACTCCACATTGC	10529
rs61096067	in-del	-/AA			intron-variant	NEBL	GRCh38.p7	10:20980063	CCACAAAAAAAAAAA[-/AA]CAAACCATAAAATTC	10529
rs61105648	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21064225	TTAACGTCAAAAAAA[A/T]TGAATTCAAATGAAT	10529
rs61142579	snp	C/G	0.0322114	0.122752	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20846307	AAGTAAATAAATTCT[C/G]CATGAAATTGTTATT	10529
rs61146312	snp	A/C	0.122411	0.214991	intron-variant	NEBL	GRCh38.p7	10:20814345	TCGTATCTGTAATCA[A/C]AGCACTTTGGAAAGC	10529
rs61153696	snp	C/T			utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20780313	AAAATTAGAATTGTA[C/T]TATTGAGGACATATG	10529
rs61187380	snp	C/T	0.0345262	0.126772	intron-variant	NEBL	GRCh38.p7	10:20805288	TAATCATTTGAATAC[C/T]GACATCAGGTGCCAA	10529
rs61188943	snp	A/C	0.335101	0.23507	intron-variant	NEBL	GRCh38.p7	10:21119484	ATATATAGTTATATT[A/C]ATATACTGAATATAA	10529
rs61230563	snp	C/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20856750	CCATTCCCTGTTCAA[C/T]AGCCTGGGAACATTA	10529
rs61234594	in-del	-/AA			intron-variant	NEBL	GRCh38.p7	10:21082564	AAAAAAAAAAAAAAA[-/AA]TTAAGACTGTGTAGA	10529
rs61269902	snp	A/C	0.0869089	0.189476	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20878082	TTACTGTTTGGAGAT[A/C]ATTTAATTTTGGGGT	10529
rs61375387	snp	G/T	0.0275645	0.114116	intron-variant	NEBL	GRCh38.p7	10:20804770	ATTAGTTCAGAGCAG[G/T]GACCGGGGCCCAAGA	10529
rs61392565	snp	C/T	0.00795532	0.062565	downstream-variant-500B	NEBL	GRCh38.p7	10:20779489	TTGACACGTGTGGAT[C/T]ATGGAGATTATAGGG	10529
rs61436063	snp	C/T	0.0387552	0.1337	intron-variant	NEBL	GRCh38.p7	10:21026060	CTCTCATGAAGTTGC[C/T]GCTGGAATCACATGA	10529
rs61477654	in-del	-/A	0.197393	0.244402	intron-variant	NEBL	GRCh38.p7	10:21040338	AGTAAGACTCCATTC[-/A]AAAAAAAAAGAAAGA	10529
rs61495623	snp	A/G	0.00517822	0.0506191	intron-variant	NEBL	GRCh38.p7	10:21035687	AAGAAGAACTTTGTG[A/G]AAGGTCTGAACTAGA	10529
rs61503787	snp	C/T	0.0170251	0.090679	intron-variant	NEBL	GRCh38.p7	10:21051897	TCACCTATGAGGGTG[C/T]GGTGGTGTGCTGGCC	10529
rs61505666	snp	C/T	0.112631	0.208878	intron-variant	NEBL	GRCh38.p7	10:21159348	AGAACCTAAGATTTC[C/T]TGAACAAGCACAGCC	10529
rs61509314	snp	C/G	0.0685596	0.171987	intron-variant	NEBL	GRCh38.p7	10:20814471	AAAAATTAGTTGGGC[C/G]TGTGCCTGTAGTCCC	10529
rs61561923	snp	C/T	0.0689305	0.172377	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21138846	AAAAAAAAAGATTAA[C/T]GGGACAGAATATCTG	10529
rs61567239	in-del	-/CAG/CAGT			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21132034	AATGTATAATTCAGT[-/CAG/CAGT]TTTAGTATATTCTCA	10529
rs61585587	in-del	-/AATTAAAAGG			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21127740	GCAACAAATAAAGGG[-/AATTAAAAGG]GGGAAAGGAGTGGAA	10529
rs61612063	snp	A/G	0.131381	0.220067	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20784190	CAGTTTTGCTTTTTC[A/G]GTTTTGTCATAGCTG	10529
rs61617198	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21058083	AGCTCAGCATGTTTT[C/T]TCAGAAATGATACTA	10529
rs61617438	in-del	-/AC	0.503416	0.0663629	intron-variant	NEBL	GRCh38.p7	10:21046006	CACACACACACACAC[-/AC]GTGTGTGCACTGGAA	10529
rs61642724	in-del	-/TTTTT	0	0	intron-variant	NEBL	GRCh38.p7	10:21003019	TTTTTTTTTTTTTTT[-/TTTTT]CAAATTTAGCCCTAA	10529
rs61676887	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21034049	GCACACACCTGTAGT[C/T]TCAGCTACTAGGGGG	10529
rs61686788	in-del	-/TAATATAACATATATAGTTATATTAATATACT			intron-variant	NEBL	GRCh38.p7	10:21119428	TATTTGTAATATACT[lengthTooLong]GAATATAACATATAT	10529
rs61711648	snp	A/T	0.49263	0.0602539	intron-variant	NEBL	GRCh38.p7	10:20803814	CTTCTGTACGAAAAA[A/T]ATATATATATATATA	10529
rs61849059	snp	A/C			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20877819	AACCGACTCCTCAAG[A/C]CTGTCTATAAAATCC	10529
rs61849664	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:20934038	TCATTAATGTTGAAA[A/T]TTAAAAAAAAAGGCC	10529
rs61849666	snp	C/T	0.0633504	0.166319	intron-variant	NEBL	GRCh38.p7	10:20964782	ATAATGAAGTCAACA[C/T]AGAGGCAAGCAAAAG	10529
rs61849667	snp	C/T	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20972344	TATTGATCAGGCAAA[C/T]ACCAACTGTTTTTCT	10529
rs61849668	snp	C/T	0.304937	0.243889	intron-variant	NEBL	GRCh38.p7	10:20972346	TTGATCAGGCAAACA[C/T]CAACTGTTTTTCTAT	10529
rs61849669	snp	C/T	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20981208	TAAAGATAGAGAACA[C/T]ATAAAGTTCAAAATA	10529
rs61849670	snp	C/T	0.0637235	0.166737	intron-variant	NEBL	GRCh38.p7	10:20982198	GGTTTAGGAATGCAT[C/T]GTGTAGTTACAGAAA	10529
rs61849671	snp	G/T	0.046775	0.145601	intron-variant	NEBL	GRCh38.p7	10:20992804	TTTTTTTGAGGCGGA[G/T]TCTCGCTCTGTCACC	10529
rs61849672	snp	A/G	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20993035	TGATCTGCCCGCCTC[A/G]GCCTCCCAAAGTGCT	10529
rs61849674	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21012496	TCCTAAGTAGCTGGG[A/G]CTACAAGCATGAGCC	10529
rs61849675	snp	C/T	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21014354	CCTGAGAGTAAGGGC[C/T]TCATCTGGTTTCACT	10529
rs61849676	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21017841	TTTTTTTTTTTTCCC[C/T]AAAATAGAGTCTTGC	10529
rs61849677	snp	A/G	0	0	intron-variant	NEBL	GRCh38.p7	10:21024065	AAAAAGTGTTACTCT[A/G]GGGAAAAAAAAAAAA	10529
rs61849813	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21026381	GTCAACAGTGCTGAG[A/G]TTAATAAGTCTTGTT	10529
rs61849814	snp	A/C	0.299664	0.245017	intron-variant	NEBL	GRCh38.p7	10:21029743	GGCCCATGCCGGGAT[A/C]TGGATCGATATGGCT	10529
rs61849830	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21071899	TCTTGGCTCACTGCA[A/G]CCTCTGTCTCCTGGG	10529
rs61849831	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21071904	GCTCACTGCAGCCTC[C/T]GTCTCCTGGGTTCAA	10529
rs61849832	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21071917	TCTGTCTCCTGGGTT[C/T]AAGCAATTCTCATGC	10529
rs61851466	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21095334	CCTAAGAAAAGCAGA[G/T]AAAAGATAAGACGAA	10529
rs61851468	snp	C/T	0.174932	0.238463	intron-variant	NEBL	GRCh38.p7	10:21104943	CAAGAATTGATGTTG[C/T]GCATAGTAAAATGCT	10529
rs61851469	snp	A/G	0.203882	0.245709	intron-variant	NEBL	GRCh38.p7	10:21112108	GATGCTGGAGAGGAT[A/G]TGGAGAAATAGGAAT	10529
rs61851471	snp	G/T	0.19459	0.243782	intron-variant	NEBL	GRCh38.p7	10:21115418	AGCCTTCTGTTAACA[G/T]TTCCTGTACTGATGG	10529
rs61851472	snp	A/G	0.0158469	0.0875917	intron-variant	NEBL	GRCh38.p7	10:21118423	AGTAAAATCCTGAAC[A/G]CATACTTAAAAAGAA	10529
rs61851473	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21125079	GAAACATCTCAAAAG[C/T]AAGCCATAAGGAACA	10529
rs61851474	snp	A/T			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21138820	CACCAAACTAAACTA[A/T]TTAAAAAAAAAAAAA	10529
rs61851501	snp	G/T			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21142999	TTAAGTGTGTGTGGG[G/T]TGTGTGTGTGTGTGG	10529
rs61851502	snp	C/G	0.5	0	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21143348	CAGCTACTTGGGAGG[C/G]TGAGGCAGGAGAATA	10529
rs61851503	snp	A/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21163751	AGACCACCAGTCTGG[A/T]TATTGATCAGATGCT	10529
rs61851760	snp	A/C	0.5	0	intron-variant, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20879876	ATTACTCTTCTAGGC[A/C]ACCAGGATGGTGGTG	10529
rs61851776	snp	A/G	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20933930	ATTAGGAGTTTCTCA[A/G]TTCAGTATATGGCCA	10529
rs61855728	snp	A/G	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20809252	ATCAAGCCATCATTC[A/G]TACCCCAACTATTCA	10529
rs61855729	snp	C/T	0.0558544	0.157504	intron-variant	NEBL	GRCh38.p7	10:20809315	AAGTTAAAAGCCAAC[C/T]ATGCTTGCCATGTAA	10529
rs61855730	snp	A/T	0.0562307	0.157967	intron-variant	NEBL	GRCh38.p7	10:20829184	TCTGATTCCAAAATC[A/T]GTGAAGTTAATTATT	10529
rs61855731	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:20830967	ACTCAAAACAAGGAG[C/G]CCCGACAGAGAGGCT	10529
rs61855732	snp	A/C	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20836332	GGTTCAAGCGATTCT[A/C]CAGCCTCAGCCTCCC	10529
rs61855733	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20841428	TGGTACTTGAAAGCA[A/G]ATACTTCAAGCACTA	10529
rs61855734	snp	G/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20849808	TCATGATTTTGACCA[G/T]GTGCTAAAACATTAA	10529
rs66476160	in-del	-/T	0.455263	0.142713	intron-variant	NEBL	GRCh38.p7	10:21120681	ATAGGTGGTCCTGGG[-/T]TTTTTTTTTTTTTTT	10529
rs66906835	snp	C/T	0.351418	0.228505	intron-variant	NEBL	GRCh38.p7	10:21069010	CCTCCCATCTCACTC[C/T]CCCGAGTAGCTGGGA	10529
rs66971038	in-del	-/A			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21141068	ATTCGACAAAAAAAA[-/A]AAAAAACCTGCTCTA	10529
rs67003579	snp	C/T	0.346368	0.23068	intron-variant	NEBL	GRCh38.p7	10:21068933	CTCTGTCACCCAGAC[C/T]ACAGTGTACAAGTGG	10529
rs67139133	snp	G/T	0.32885	0.23724	intron-variant	NEBL	GRCh38.p7	10:21119428	TATTTGTAATATACT[G/T]AATATAACATATATA	10529
rs67214625	in-del	-/C			intron-variant	NEBL	GRCh38.p7	10:20900855	ATTTTTTTCTTTTTT[-/C]TTTTTTTTTCGGGAT	10529
rs67288319	in-del	-/A	0.474716	0.109556	intron-variant	NEBL	GRCh38.p7	10:20888228	GGAAAAAAAAACAGG[-/A]AAAAAATAAATAAAT	10529
rs67403859	snp	G/T	0.15665	0.231917	intron-variant	NEBL	GRCh38.p7	10:20967281	TAAGTGAATCATGGA[G/T]CTATGTGGATGAGTC	10529
rs67559061	in-del	-/AAGAG/AG/AGAGC			intron-variant	NEBL	GRCh38.p7	10:21095335	TAAGAAAAGCAGATA[-/AAGAG/AG/AGAGC]AAAGATAAGACGAAC	10529
rs67586893	in-del	-/CTCA	0.43978	0.162738	intron-variant	NEBL	GRCh38.p7	10:21098215	ACATACACACACATT[-/CTCA]CTCACACGTGCACAC	10529
rs67817499	snp	C/T	0.275464	0.2487	intron-variant	NEBL	GRCh38.p7	10:20978373	TAATATACAAGGCCA[C/T]TTGTGAGTCTATCCT	10529
rs67902595	snp	C/G	0.308661	0.24302	intron-variant	NEBL	GRCh38.p7	10:20989948	TTACTGCTGAAATAT[C/G]AGCAGAACCTGTGAT	10529
rs67955617	snp	C/T	0.356383	0.226236	intron-variant	NEBL	GRCh38.p7	10:20979749	TCTCACTCTGTCACC[C/T]GCGCTGGAATACAGT	10529
rs68140601	snp	C/G	0.15665	0.231917	intron-variant	NEBL	GRCh38.p7	10:20964807	CAAAAGAGTGATTGA[C/G]AGAGAGTCCTGACAT	10529
rs68150492	in-del	-/CTTA			intron-variant	NEBL	GRCh38.p7	10:21066823	TCTTACATTGTTCTG[-/CTTA]CGGTTTTTCTATTTA	10529
rs71390794	in-del	-/A	0	0	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20854562	AGCAAGACCCTGTCC[-/A]AAAAAAAAAAAAAAA	10529
rs71390795	in-del	-/TG/TTG	0	0	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20855523	TCGTTTTTTTTTTGT[-/TG/TTG]TTTGTTTTGTTTTCT	10529
rs71390796	in-del	-/T	0	0	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20855534	TAAGTTTTCCTTCGT[-/T]TTTTTTTTGTTTGTT	10529
rs71390798	in-del	-/AAAAAAAAAA	0	0	intron-variant	NEBL	GRCh38.p7	10:20914983	AAACCCCATCTCTCC[-/AAAAAAAAAA]AAAAAAAAAAAAAAT	10529
rs71390799	in-del	-/TTTTTTT	0	0	intron-variant	NEBL	GRCh38.p7	10:20923696	TCAAGAAACCATTTC[-/TTTTTTT]TTTTTTTTTTTTTTT	10529
rs71390800	in-del	-/T	0	0	intron-variant	NEBL	GRCh38.p7	10:20924438	AGGAAAGGTGTAGCC[-/T]TTTTTTTTTTTTTTT	10529
rs71390801	in-del	-/T	0	0	intron-variant	NEBL	GRCh38.p7	10:20952459	TCCTATTTCCAGTTC[-/T]TTTTTTTTTTTTTTT	10529
rs71392103	in-del	-/TTT	0	0	intron-variant	NEBL	GRCh38.p7	10:20997512	TCTTCAGGAGTTCTG[-/TTT]TTTTTTTTTTTTTTT	10529
rs71392105	in-del	-/TTTT	0	0	intron-variant	NEBL	GRCh38.p7	10:21028247	TCTTCTTCTTCTTTT[-/TTTT]TTTTTTTTTTTTTGA	10529
rs71392106	in-del	-/TTCTTCTTCTTCTTCTTCTTCTTCTTCTTC	0	0	intron-variant	NEBL	GRCh38.p7	10:21028274	TTTTATTTCTCATTC[lengthTooLong]TTCTTCTTCTTCTTC	10529
rs71392108	in-del	-/CT/TC	0	0	intron-variant	NEBL	GRCh38.p7	10:21033754	TTTCTTTTCTTTCTT[-/CT/TC]TTTTTTTTTTTTTCG	10529
rs71392110	in-del	-/TATTTA	0	0	intron-variant	NEBL	GRCh38.p7	10:21061572	AACTTAAGACAATGC[-/TATTTA]TATTTATATTTATAT	10529
rs71392111	in-del	-/TTTATA	0	0	intron-variant	NEBL	GRCh38.p7	10:21063913	TGCTAATTTTTTTTG[-/TTTATA]TTTATATTTATATTT	10529
rs71392112	in-del	-/TTTTTTTTTTTTT	0.0486741	0.148216	intron-variant	NEBL	GRCh38.p7	10:21082536	TTTTTTTTTTTTTTT[-/TTTTTTTTTTTTT]AGTGGTGGTGGGGAA	10529
rs71392113	in-del	-/AAAAA	0	0	intron-variant	NEBL	GRCh38.p7	10:21082780	GTGAGACTCTGTCTC[-/AAAAA]AAAAAAAAAAAAAAA	10529
rs71486474	snp	A/C	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20789973	TATATATATATACAC[A/C]CACACACATACAAGT	10529
rs71486475	snp	A/C	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20796363	GAAACTCAGTCTAAA[A/C]CAAGAAAAAAAAAAA	10529
rs71486476	snp	A/G	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20796368	TCAGTCTAAAACAAG[A/G]AAAAAAAAAAAAAAA	10529
rs71486477	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20800204	TTTCAGATTCCACAT[A/G]TAAGTGGGATCATGC	10529
rs71486478	snp	A/C	0.5	0	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20851466	GAAGTATAATAACAC[A/C]CAACACTAGGATAGA	10529
rs71486479	snp	A/C	0.5	0	intron-variant, utr-variant-5-prime, upstream-variant-2KB	NEBL	GRCh38.p7	10:20959120	CTAAGAAAGAGCCAC[A/C]CAATATTCAGAGATA	10529
rs71486480	snp	C/G	0.00279258	0.0372817	intron-variant	NEBL	GRCh38.p7	10:20982122	CGTTCAATTACCCAC[C/G]CTAACAGAAAAGTGG	10529
rs71486481	snp	C/T	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20997466	AAATAAACGCACAGT[C/T]TCAGTAAAAAAAAAA	10529
rs71486482	snp	C/T	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21022002	CAAACATTCAGCGGC[C/T]TCTTATGTTCACAGA	10529
rs71486483	snp	C/T	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21076276	GGCAAAACCCCATCT[C/T]TACTAAAAATACAAA	10529
rs71486484	snp	A/C	0.0193772	0.0965046	intron-variant	NEBL	GRCh38.p7	10:21090808	CTGGCCCCTGCTGTT[A/C]ACTTCCTGTTTGTGG	10529
rs71486485	snp	C/T	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21095320	CAGGGAAATTCTAGC[C/T]TAAGAAAAGCAGATA	10529
rs71486486	snp	A/G	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21153460	TCAGCCTCCTGAATA[A/G]CTGGGATTACAGGTG	10529
rs71486487	snp	C/T	0.0189856	0.0955633	intron-variant	NEBL	GRCh38.p7	10:21168733	GATGTATGAAACCAA[C/T]TTGATGTATGAAATG	10529
rs71509085	in-del	-/C	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20818039	GTGAAGTCCATTCCC[-/C]TGTCACCCTAGAAGG	10529
rs71509086	in-del	-/C	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21071979	CCTGCCACCACACCC[-/C]AGCTAATTTTTGTGT	10529
rs71509087	multinucleotide-polymorphism	AA/TC	0.5	0	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21139985	TTGAAACCCTGTCTC[AA/TC]CAAAAAAAAAAAAAA	10529
rs71524337	snp	A/G	0.00914312	0.0669923	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20857980	AAGGGAAAGAAGAAT[A/G]ATGGAAAGGCCACTG	10529
rs71524341	snp	A/G			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20857681	CTGACCACGTGGGCA[A/G]TGCACCCAGATATTT	10529
rs71524343	snp	A/G	0.00279162	0.0372561	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20852482	ACGGCAGTGAGCGGC[A/G]GGCCTCAGGATGGTT	10529
rs71526495	snp	C/T	0.0107246	0.0724382	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20857836	AAAATACAGTTTAGA[C/T]TAAGACAATTTTTCA	10529
rs71534253	snp	A/G	0.00286854	0.0377629	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20852541	CGTACGGGCAAGTGT[A/G]TACCTGACTTTGGAG	10529
rs71535728	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20831688	TCTTTTGGAATGAAG[C/T]TGAATCCTTATTTCT	10529
rs71535729	snp	C/T	0.000916628	0.0213886	intron-variant	NEBL	GRCh38.p7	10:20831166	TGACATTGGAATACA[C/T]GATTCTGAGCATCTT	10529
rs71535731	snp	A/G	0.0618563	0.164627	intron-variant	NEBL	GRCh38.p7	10:20819852	GACTCGGCCTCCCAA[A/G]GTGCTGGGATTACAG	10529
rs71535732	snp	C/T	0.0322266	0.122779	intron-variant, missense, synonymous-codon, nc-transcript-variant	NEBL	GRCh38.p7	10:20815684	GAGTTACACTTAAAG[C/T]GGTAGCTCTTCCCAG	10529
rs71535733	snp	C/T	0.00199481	0.0315187	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20783026	AGAAAGTCAGGTGCA[C/T]GCTCTCTGTGCTTGG	10529
rs71541562	snp	C/T	0.000280355	0.0118363	intron-variant, missense, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20869799	GTCGGTCAAGTTCTG[C/T]ACTGTACGTGTGGGT	10529
rs71541563	snp	C/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20869503	ATACCTAAATAGTAT[C/T]TATTTCTCTAAAAGT	10529
rs71541564	snp	A/T	0	0	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20868849	CAAAAAAAAAAAAAA[A/T]AACAGACCTTCATCT	10529
rs71541566	snp	C/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20860190	TTTAGAAAATAGATT[C/T]TAGGCCCCAGAATTT	10529
rs71541567	snp	A/T	0.00557542	0.0525036	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20860131	TTTCTATAATCTATG[A/T]TCAGTTAGAAACCTA	10529
rs71541568	snp	C/T	0.00557542	0.0525036	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20858596	GTAATGTCAATAGAA[C/T]AAAGTAATTTTCACA	10529
rs71541569	snp	A/G/T	3.56011e-05	0.00421892	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20858376	GAACAAAATACCATC[A/G/T]AGGAGAAGAAAATAT	10529
rs71578938	snp	A/C	0.00380012	0.0434237	intron-variant, upstream-variant-2KB	NEBL, LOC102725112	GRCh38.p7	10:20845374	TGTAAACTTTCTGTT[A/C]AATAAGACCACATAA	10529
rs71578939	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NEBL, LOC102725112	GRCh38.p7	10:20845087	AATGTTAACACACAC[G/T]TTCTTGTTTCTAATG	10529
rs71578940	snp	C/T			intron-variant, upstream-variant-2KB	NEBL, LOC102725112	GRCh38.p7	10:20845051	AAATCTGGGTAATTT[C/T]TTCTCGCAACTTTAA	10529
rs71578941	snp	C/T	0.00676609	0.0577691	intron-variant	NEBL	GRCh38.p7	10:20835323	AGCTTTCTTGATATA[C/T]TGGAAGGATATGAGC	10529
rs71578942	snp	A/G	0.00597247	0.0543191	intron-variant	NEBL	GRCh38.p7	10:20831398	AAAGCCACCCATGTG[A/G]AAAGAAAACTTATGC	10529
rs71578943	snp	C/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20828311	AACTGTCATTTATAC[C/T]GAAGAGGAAATTTTG	10529
rs71578944	snp	A/C	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20826704	ATCCATTCAGATAAT[A/C]CATGAAAACTTTGGT	10529
rs71578946	snp	A/G	0.0199855	0.0979469	intron-variant	NEBL	GRCh38.p7	10:20826418	TGGTTTGCTTTTAGA[A/G]AAGATAATTAATGCT	10529
rs71578947	snp	A/C	0.0256215	0.110247	intron-variant	NEBL	GRCh38.p7	10:20826296	ACAGTTTTTGTTCTG[A/C]AAGTTAGATCTTTGA	10529
rs71578949	snp	C/T	0.0839998	0.186933	intron-variant	NEBL	GRCh38.p7	10:20819777	TTGTCCAGGCTGGAG[C/T]GCAGTGGCGTCATCA	10529
rs71578950	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:20819576	TACGTCCCAAAACAT[G/T]GCAACAGATTTTTTT	10529
rs71578951	snp	A/C/G/T	0.000148479	0.00861513	intron-variant	NEBL	GRCh38.p7	10:20819563	TATGGGAAATAAATA[A/C/G/T]GTCCCAAAACATTGC	10529
rs71578953	snp	C/T	0.0528381	0.153711	intron-variant, nc-transcript-variant	NEBL	GRCh38.p7	10:20819299	TTTAGCTCTCATTAT[C/T]ATGCAGTATTTGGTT	10529
rs71578954	snp	C/G	0.00119737	0.0244387	intron-variant, downstream-variant-500B	NEBL	GRCh38.p7	10:20817477	TCTTTCAAATAAGTT[C/G]TTAGTCAAATGAGAA	10529
rs71578955	snp	C/T	0.0410537	0.137264	intron-variant	NEBL	GRCh38.p7	10:20815856	TCACCACAGCCTCGA[C/T]CTCCCAGGCTCAGGC	10529
rs71578956	snp	C/T	0.0150112	0.0853245	NEBL	10	allele_origin=T(germline)/C(germline)	10:20815722	CTGTAATAAACCTAT[C/T]ATTTCAGAGAACAAA	10529
rs71578957	snp	A/G	0.000165169	0.0090861	intron-variant, missense, utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20815626	AGAAAACCACTTGCC[A/G]AGCTAATATTTTCTT	10529
rs71578958	snp	A/G	0.0486741	0.148216	intron-variant, downstream-variant-500B	NEBL	GRCh38.p7	10:20815557	ATTTTCACAAGCAAA[A/G]GAGGACCGCAAGTAA	10529
rs71578959	snp	C/T	0.0391387	0.134304	intron-variant	NEBL	GRCh38.p7	10:20814323	AAACCTGCGCAAGCC[C/T]GAGGACTCGTATCTG	10529
rs71578960	snp	A/G	0.0391387	0.134304	intron-variant	NEBL	GRCh38.p7	10:20814319	CTGTAAACCTGCGCA[A/G]GCCCGAGGACTCGTA	10529
rs71578961	snp	A/T	0.0337553	0.125452	intron-variant	NEBL	GRCh38.p7	10:20814238	TCCACCGCCTACTGC[A/T]AAATGACCTAAATCT	10529
rs71578962	snp	C/G	0.0131001	0.0798652	intron-variant, nc-transcript-variant	NEBL	GRCh38.p7	10:20813895	CGTGCACTGGATCCG[C/G]CCATTCCTTAGCATG	10529
rs71578963	snp	C/T	0.0360663	0.129354	intron-variant	NEBL	GRCh38.p7	10:20812579	AAAGACTTGAGATGA[C/T]ACCAGGTGAATGCCA	10529
rs71578966	snp	C/T	0.029116	0.117091	intron-variant	NEBL	GRCh38.p7	10:20812481	CCCCCTCCCCCCACC[C/T]CACAACAGGCCCTGG	10529
rs71578967	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20812475	TCCCTCCCCCCTCCC[C/T]CCACCTCACAACAGG	10529
rs71578968	snp	A/C/G	3.33524e-05	0.00408354	intron-variant	NEBL	GRCh38.p7	10:20809924	AAGGAAGAAATCAAC[A/C/G]CTCATCAAGAAGGAA	10529
rs71578969	snp	C/T	0.0383715	0.133092	intron-variant	NEBL	GRCh38.p7	10:20809746	AACCTCTACAGTTCA[C/T]AGTGGTTCACTTTTG	10529
rs71578971	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20783079	CTCAATTTTTAAAAT[A/C]TTCTTTAGCTGTCAG	10529
rs71578974	snp	A/G	0.00119737	0.0244387	intron-variant, utr-variant-5-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20897289	CCTTGAGATGCTGAC[A/G]TCTCTGGTGCTCTGG	10529
rs71578975	snp	C/T	0.00487112	0.0491104	intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20889912	GTCACAAATGTACAC[C/T]TATCCTTGGACTTTT	10529
rs71578977	snp	A/G	0.127944	0.218179	intron-variant	NEBL	GRCh38.p7	10:20889601	AGGAATCGTATATAA[A/G]TAAGAAAGATTTAGA	10529
rs71578979	in-del	-/A	0.00852008	0.0647105	NEBL	10	allele_origin=A(germline)/(germline)	10:20888215	TATTTTGCCTGGGGG[-/A]AAAAAAAACAGGAAA	10529
rs71578981	snp	C/T	0.00914312	0.0669923	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20881132	GTCCTTGACCAAAGA[C/T]GAAATTTCCATTTTT	10529
rs71578983	snp	C/T	0.00647296	0.0565206	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20880791	AGAAATGCGCTTCCT[C/T]ACATTACTCTGGTGT	10529
rs71701700	in-del	-/A	0.135143	0.222054	downstream-variant-500B	NEBL	GRCh38.p7	10:20779749	ATTATTTTTTGTCAG[-/A]AAAAAAAAAATCTAA	10529
rs71747504	in-del	-/TTG			intron-variant	NEBL	GRCh38.p7	10:21074796	TAGATATATATATTT[-/TTG]TTGTTGTTGTTGTTG	10529
rs71857534	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:20796394	AAAAAAAAAAAAAAA[-/A]CTTCTCTAAAATATT	10529
rs72021692	in-del	-/AA			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21143448	GTGAAACTTCATCTC[-/AA]AAAAAAAAAAAAAAA	10529
rs72062179	in-del	-/AT			intron-variant	NEBL	GRCh38.p7	10:21125224	CACATGCACACATGC[-/AT]ATACACACACACACA	10529
rs72102767	in-del	-/CACT	0.336311	0.234628	frameshift-variant, intron-variant	C10orf113, NEBL	GRCh38.p7	10:21146412	TTAGTAAAGCACAAA[-/CACT]CTCTCTCATATAAGC	10529
rs72230657	in-del	-/GTGTGT			intron-variant	NEBL	GRCh38.p7	10:21096489	GCAACTTGGTTTTGA[-/GTGTGT]GTGTGTGTGTGTGTG	10529
rs72278772	in-del	-/A	0	0	intron-variant	NEBL	GRCh38.p7	10:21094532	AAAAAAAAAAAAAAA[-/A]TTAGCCAGATGTGGT	10529
rs72447354	in-del	-/TTTTT			intron-variant	NEBL	GRCh38.p7	10:21066986	TGAAATAATTTAACT[-/TTTTT]TTTTTTTTTTTTTTT	10529
rs72481156	snp	A/T	0.0236746	0.106192	intron-variant	NEBL	GRCh38.p7	10:20929443	TTGAAAATTGTAACC[A/T]CAGCAATCCCTAACT	10529
rs72481157	snp	C/T	0.0236746	0.106192	intron-variant	NEBL	GRCh38.p7	10:20930253	CAAAATTCTAGGAGA[C/T]GTTCTTGTTTTCCCT	10529
rs72513862	in-del	-/G	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21091524	TCCAATTAGCTATCA[-/G]GTACCTCAAGTTTCC	10529
rs72648287	snp	A/T			utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20784359	CAGCAAGGGCTAGCA[A/T]AAAGCCTGCAAAGTC	10529
rs72785552	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20791257	ATGTCTCTTCTACTG[C/T]ACAATAAAGTACTTC	10529
rs72785555	snp	A/G	0.117188	0.211804	intron-variant	NEBL	GRCh38.p7	10:20794401	TCCTGTTTATAGTAT[A/G]TACTATATCCTGCTT	10529
rs72785564	snp	C/T	0.370365	0.219117	intron-variant	NEBL	GRCh38.p7	10:20805348	TTAAATTAGCATATT[C/T]CAATGTATCCTAAAA	10529
rs72785566	snp	A/G	0.067446	0.170804	intron-variant	NEBL	GRCh38.p7	10:20806548	TGACATCAAGGCCAG[A/G]TGCAGCTGCGCTGTT	10529
rs72785567	snp	C/G	0.123798	0.215808	intron-variant	NEBL	GRCh38.p7	10:20806721	CTGTGTGCATTGCCA[C/G]ATCTAAGCTCTTGGC	10529
rs72785575	snp	C/T	0.00478085	0.0486577	intron-variant	NEBL	GRCh38.p7	10:20822408	TTTCATAAATATATA[C/T]ATTCATAGATATCTA	10529
rs72785577	snp	A/G	0.00993419	0.0697739	intron-variant	NEBL	GRCh38.p7	10:20825854	GTCTAAAGGTTACTG[A/G]AAGCTAAGTTATTTC	10529
rs72785580	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20832141	TGATTTGCCACTGGA[A/C]AAGTCAATGTTCCCC	10529
rs72785594	snp	C/T	0.0441095	0.141807	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20865518	CTAGACCAAACCATA[C/T]TGCTTCTCCGGGATT	10529
rs72789322	snp	C/T	0.0437281	0.141251	intron-variant	NEBL	GRCh38.p7	10:20951604	CCCTTGACTTATGAC[C/T]CTCCAATAAGCTAAA	10529
rs72789340	snp	C/T	0.121369	0.214369	intron-variant	NEBL	GRCh38.p7	10:20964551	CACGTGAACTCATTG[C/T]TGTGGGGAGGGCAAA	10529
rs72789344	snp	C/T	0.119978	0.213528	intron-variant	NEBL	GRCh38.p7	10:20968449	CCAGAAGTTCAAGGC[C/T]GCAGTGAGCTATGTT	10529
rs72789349	snp	A/T	0.00993419	0.0697739	intron-variant	NEBL	GRCh38.p7	10:20975382	CCTACATTTCATAGT[A/T]CATGAGAGTACAGCT	10529
rs72789353	snp	C/T	0.116488	0.211364	intron-variant	NEBL	GRCh38.p7	10:20978273	TCCTCTAAGACTGAA[C/T]AGTCTAATCAGAACA	10529
rs72789354	snp	A/C	0.116488	0.211364	intron-variant	NEBL	GRCh38.p7	10:20978279	AAGACTGAATAGTCT[A/C]ATCAGAACACCAAAT	10529
rs72790523	snp	A/C	0.0283406	0.115616	intron-variant	NEBL	GRCh38.p7	10:20982729	TATGGCCTTCCCCCC[A/C]AAAAAATTTCTCACT	10529
rs72790526	snp	C/T	0.11228	0.208646	intron-variant	NEBL	GRCh38.p7	10:20986401	CAGCAACTCTTCGCT[C/T]CCCTTCAAAATTCCC	10529
rs72790536	snp	A/G	0.133777	0.221342	intron-variant	NEBL	GRCh38.p7	10:20992725	TTTACTTTCTCCGTA[A/G]GCCAACTACAATGAA	10529
rs72790553	snp	C/T	0.106278	0.204558	intron-variant	NEBL	GRCh38.p7	10:21006522	ACCAGTCCTTCTTCC[C/T]TGTTCCTTCCCTTGG	10529
rs72790555	snp	A/G	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:21009190	AAAGAATCAGTATTG[A/G]GGCTCTATGACTGCC	10529
rs72790563	snp	A/G	0.0894459	0.191631	intron-variant	NEBL	GRCh38.p7	10:21013059	TTTGTCTCTTACATC[A/G]TTTTATCCAGGGGTA	10529
rs72790573	snp	C/T	0.140919	0.224948	intron-variant	NEBL	GRCh38.p7	10:21024629	TCATACTGCCTTATA[C/T]TGAAAATGAAAATTA	10529
rs72790575	snp	C/T	0.0887219	0.191022	intron-variant	NEBL	GRCh38.p7	10:21024794	CAATCTCAACTTCCA[C/T]TCACCCACCACTCCA	10529
rs72790576	snp	A/G	0.0640965	0.167152	intron-variant	NEBL	GRCh38.p7	10:21025520	GTTGTTAAAAATATA[A/G]GAAAAGTTATATGCA	10529
rs72790578	snp	A/T	0.0626037	0.165477	intron-variant	NEBL	GRCh38.p7	10:21025594	CATAAGCAAATGGCA[A/T]CCTCCATGGAGATGG	10529
rs72790586	snp	C/T	0.0422008	0.138995	intron-variant	NEBL	GRCh38.p7	10:21039564	GGACATTTTCTATGA[C/T]GACAAGAAGATTCAA	10529
rs72791975	snp	G/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20868435	ATTGAAAAATGTTCA[G/T]ATTTATGCCTGGAGA	10529
rs72791983	snp	C/T	0.00478085	0.0486577	intron-variant	NEBL	GRCh38.p7	10:20890438	TATTACCGTTATTAC[C/T]TAGACATGCTTGATT	10529
rs72793911	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:20910835	TCGTTTTTGTTTTTT[G/T]TTTTTTGGCCAAAGG	10529
rs72793917	snp	C/T	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20914931	GGCACAATCTTGACT[C/T]ATGCAATTCTCCTAC	10529
rs72793932	snp	C/T	0.116138	0.211142	intron-variant	NEBL	GRCh38.p7	10:20924190	TCATGATTAGAGGCT[C/T]TTATTGGCATTTCAT	10529
rs72796554	snp	C/G	0.0244538	0.107838	intron-variant	NEBL	GRCh38.p7	10:21090273	GGATATCTTCTAAAT[C/G]ACAAGGGCACAAGTA	10529
rs72796574	snp	A/G	0.0151789	0.085785	missense, intron-variant, synonymous-codon	C10orf113, NEBL	GRCh38.p7	10:21126107	CCTTCTCGGCTCTCC[A/G]TTCTGCCTTACCAGG	10529
rs72796576	snp	C/T	0.0162398	0.0886349	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21129124	TAAAGGAATTTGTTG[C/T]CAATACACCTGCCTT	10529
rs72796582	snp	C/T	0.00597247	0.0543191	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21142675	TCAGGGGCCCCCAAC[C/T]CCCAGGGCGGCAGAC	10529
rs72796590	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21149670	TAGCAAATTAACAGA[A/C]TCCAAGGACAGAGTT	10529
rs72798503	snp	C/T	0.245346	0.249957	intron-variant	NEBL	GRCh38.p7	10:21165986	TTTCTATTGGGAGGC[C/T]GATGTGGGAGGATCA	10529
rs73607513	snp	A/G	0.0170251	0.090679	intron-variant	NEBL	GRCh38.p7	10:20789795	GAGGTCAAGGCTGCC[A/G]TGTGATCTCACCACT	10529
rs73607514	snp	C/T	0.0166325	0.0896639	intron-variant	NEBL	GRCh38.p7	10:20799824	TCTTCTTAAATAAAG[C/T]TCATGTATATTTGAA	10529
rs73607515	snp	G/T	0.0441095	0.141807	intron-variant	NEBL	GRCh38.p7	10:20803857	CACATACTGGGAATG[G/T]TTTCACTTTAGAGTA	10529
rs73607516	snp	A/C	0.0298908	0.118541	intron-variant	NEBL	GRCh38.p7	10:20805122	TGGGGTATGAGTGAA[A/C]GACAAGCGTCAGGGA	10529
rs73607518	snp	A/T	0.0283406	0.115616	intron-variant	NEBL	GRCh38.p7	10:20808230	TAACTCCTGTGAAAC[A/T]GACTCAAGCAGCAAG	10529
rs73607519	snp	C/T	0.0685596	0.171987	intron-variant	NEBL	GRCh38.p7	10:20816816	GCCCCTTATTAAGTG[C/T]CCCCAAAATGGTCCT	10529
rs73607520	snp	C/T	0.0225045	0.103662	intron-variant	NEBL	GRCh38.p7	10:20828160	TTAAGAATGAGTAAA[C/T]GGTTAGACATATTAT	10529
rs73607521	snp	C/T	0.0414363	0.137845	intron-variant	NEBL	GRCh38.p7	10:20834256	GTGTACATGTGTATG[C/T]TTATCTATATAAACA	10529
rs73607522	snp	A/G	0.0486741	0.148216	intron-variant	NEBL	GRCh38.p7	10:20834355	TAGGAAAGGGATAAA[A/G]CAGGTTTTCAAGTTC	10529
rs73607523	snp	C/T	0.0252325	0.109451	intron-variant	NEBL	GRCh38.p7	10:20834737	TTCACATACACTTTT[C/T]ATAAAATCATCACAT	10529
rs73607524	snp	G/T	0.0260105	0.111035	intron-variant	NEBL	GRCh38.p7	10:20837151	ACTGAGCTTAGTGAG[G/T]AAAGGATGTCAAAAG	10529
rs73607525	snp	C/T	0.0267878	0.112589	intron-variant	NEBL	GRCh38.p7	10:20839240	GTCTGTACTTTGCCA[C/T]TGAGAGAATAAAACA	10529
rs73607526	snp	C/T	0.0225045	0.103662	intron-variant, upstream-variant-2KB	NEBL, LOC102725112	GRCh38.p7	10:20844990	TATAGAGCTTCTGAG[C/T]TACAACTAAAACAAA	10529
rs73607527	snp	A/G	0.0452528	0.143452	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20845940	ATGGTGTTTGATATG[A/G]ATGAAGTTGTGCTGT	10529
rs73607528	snp	A/G	0.0295035	0.117819	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20847710	ATGTTCTCAGAAAAG[A/G]AAAGTGATTTTTGAT	10529
rs73607529	snp	C/G	0.0232847	0.105357	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20849252	TCTCGCTGGAACAGA[C/G]AAAAAAAAAGTGTGG	10529
rs73607530	snp	C/G	0.0228947	0.104514	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20851116	TTCGGTTTATAAAAT[C/G]AGTGATATTTTTTAT	10529
rs73607533	snp	A/G	0.0275645	0.114116	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20859044	GTATATTTCATCTCT[A/G]TTTCTAAGAAAGCAA	10529
rs73607534	snp	A/T	0.0379877	0.132479	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20862567	TTTTCAATCTAGAGT[A/T]CATACATCTGTGTGT	10529
rs73607535	snp	C/T	0.0448719	0.142907	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20864271	TACTTAAATCTGAGA[C/T]ACATATGCACCAATC	10529
rs73607536	snp	A/T	0.0414363	0.137845	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20867273	TTTAGGATGTTTAGT[A/T]TCAAGGCTCTTTCAC	10529
rs73607537	snp	A/G	0.0240643	0.107019	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20875980	TAGCAAAACTCTCAC[A/G]TTAGAGAAGCCCTCC	10529
rs73607538	snp	C/T	0.0551013	0.156571	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20877323	ATCCAGGGTCATCCA[C/T]GCAACGTGTGCCCAA	10529
rs73607539	snp	C/T	0.0524604	0.153226	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20877387	CTTTCCTAGTATATG[C/T]TACTGATATAGGAGT	10529
rs73607540	snp	A/G	0.138546	0.223781	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20878444	GTAATTCCACTAGTA[A/G]ATTCTCTGCAATGAG	10529
rs73607542	snp	C/G	0.0134861	0.0810011	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20883560	GAGTTTCATGGGTAC[C/G]CAAGTCTACAAAGCT	10529
rs73607543	snp	A/G	0.0134861	0.0810011	intron-variant	NEBL	GRCh38.p7	10:20886249	GGGGAAAGGTAGGGC[A/G]CAATGGCTCACACCT	10529
rs73607545	snp	A/C	0.141258	0.225111	intron-variant	NEBL	GRCh38.p7	10:20896595	AAAAAAATGACTATT[A/C]ATTTAGATAGAGGGC	10529
rs73607546	snp	A/G	0.039522	0.134904	intron-variant	NEBL	GRCh38.p7	10:20903104	GTTCCAAGCCCCCCA[A/G]TAGAAGCCTGAAAGT	10529
rs73607547	snp	G/T	0.318174	0.240525	intron-variant	NEBL	GRCh38.p7	10:20903820	TGGCAGCTAAGCTAC[G/T]GGTATGCAAAGGCAC	10529
rs73607548	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20905929	AGTTATAACAATTCC[C/T]AGTCAATTAACTGTG	10529
rs73607551	snp	C/T	0.0209421	0.100162	intron-variant	NEBL	GRCh38.p7	10:20927457	ATAGTAAATAAGACA[C/T]ATAAAAGAGTTGACT	10529
rs73607552	snp	C/T	0.0232847	0.105357	intron-variant	NEBL	GRCh38.p7	10:20927639	GTGTTCGTGTAAATA[C/T]CCTTTGCCAGTGTAA	10529
rs73607553	snp	A/C	0.0189856	0.0955633	intron-variant	NEBL	GRCh38.p7	10:20927930	CACCCAACAGAGATA[A/C]AATGTGAGCCACATA	10529
rs73607554	snp	C/T	0.0185938	0.0946107	intron-variant	NEBL	GRCh38.p7	10:20928055	ATTGTCATTTCAACA[C/T]GTTATTGATATAAAA	10529
rs73607555	snp	A/G	0.0221141	0.102801	intron-variant	NEBL	GRCh38.p7	10:20949247	TGGGAGTCATACAAC[A/G]AGAACACACGGACAC	10529
rs73607557	snp	A/G	0.0166325	0.0896639	intron-variant	NEBL	GRCh38.p7	10:20950581	TTCTGAAATCCACAC[A/G]GCCTGATGCAATGTC	10529
rs73607558	snp	A/G	0.00835141	0.0640778	intron-variant	NEBL	GRCh38.p7	10:20954954	CACTAAGCCAGGGAC[A/G]GCCTCACATTCCAGG	10529
rs73607559	snp	A/C	0.0611083	0.163768	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20961994	TTAAGCAAGTTCTTT[A/C]ACCACTCTGTGCTCA	10529
rs73607560	snp	A/G	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20963513	TTTCCAAAGACAGAG[A/G]TGAAAAGAAAAACCA	10529
rs73607562	snp	A/G	0.0225045	0.103662	intron-variant	NEBL	GRCh38.p7	10:20968842	GATGGTGAGGGTCGC[A/G]ATATTTTAAAACTAC	10529
rs73607563	snp	A/T	0.0995161	0.199636	intron-variant	NEBL	GRCh38.p7	10:20970141	GGCTCCTGTGTTCCA[A/T]GCATAGTAATGAGTG	10529
rs73607564	snp	A/C/T	0.0236882	0.106316	intron-variant	NEBL	GRCh38.p7	10:20970148	GTGTTCCAAGCATAG[A/C/T]AATGAGTGTTTTACA	10529
rs73607565	snp	A/G	0.0517044	0.152246	intron-variant	NEBL	GRCh38.p7	10:20973372	CCCACCTCAGCCCCC[A/G]GCATAGCTAGGACTT	10529
rs73607566	snp	A/G	0.0722614	0.17581	intron-variant	NEBL	GRCh38.p7	10:20989932	AAATTTAGCATACCA[A/G]TTACTGCTGAAATAT	10529
rs73607567	snp	C/T	0.0228947	0.104514	intron-variant	NEBL	GRCh38.p7	10:20990274	ACCCCTGCTTTGAAA[C/T]GTTAACAACACTTAC	10529
rs73607568	snp	C/T	0.0228947	0.104514	intron-variant	NEBL	GRCh38.p7	10:20990878	CTGATTTTCTCATTA[C/T]CAATCTGACTGCAAA	10529
rs73607569	snp	A/G	0.0115144	0.0749975	intron-variant	NEBL	GRCh38.p7	10:21004974	TGGAGAAACTGGTGA[A/G]TTAAGGGTAGGCCAT	10529
rs73607570	snp	C/T	0.0115144	0.0749975	intron-variant	NEBL	GRCh38.p7	10:21005945	TATTAATCCATATTT[C/T]TCTACCTATACATAT	10529
rs73607571	snp	A/G	0.0379877	0.132479	intron-variant	NEBL	GRCh38.p7	10:21011382	TCTTTACAAGTCCGT[A/G]CCACACGGAAGTGGA	10529
rs73607572	snp	A/G	0.030665	0.119967	intron-variant	NEBL	GRCh38.p7	10:21016965	TTAATGCCAAATTCT[A/G]CCTTTACATACATTG	10529
rs73607573	snp	C/G/T	0.0197687	0.0974348	intron-variant	NEBL	GRCh38.p7	10:21022253	CCTTTCTGGTATCCA[C/G/T]GTGTGTCTCTTCCTG	10529
rs73607576	snp	C/T	0.00993419	0.0697739	intron-variant	NEBL	GRCh38.p7	10:21030345	CTGGGACCTCCGCCA[C/T]ACCCGGCAAAAGTCA	10529
rs73607577	snp	A/G	0.0103295	0.0711199	intron-variant	NEBL	GRCh38.p7	10:21030974	GCACTGATGACCATC[A/G]CCCTGCCTCCAACAG	10529
rs73607578	snp	C/T	0.0376037	0.131863	intron-variant	NEBL	GRCh38.p7	10:21033183	CGGCACTGTTGATTA[C/T]AGCCAAGAGAAACAC	10529
rs73607579	snp	C/T	0.0379877	0.132479	intron-variant	NEBL	GRCh38.p7	10:21035348	GCCCCCCAAAATTAG[C/T]ATATTTTACAACAGT	10529
rs73607580	snp	C/T	0.0364509	0.129988	intron-variant	NEBL	GRCh38.p7	10:21037911	AGGGAGTAAGAACCA[C/T]TTGCATCTTCACCTC	10529
rs73607581	snp	A/G	0.182296	0.240658	intron-variant	NEBL	GRCh38.p7	10:21043926	GAGTGGAGAGATCCT[A/G]GTCTACAACTCTAAA	10529
rs73607582	snp	C/G	0.0345262	0.126772	intron-variant	NEBL	GRCh38.p7	10:21046081	AATCCCGTCATTTGT[C/G]ACAACATGGATAAAA	10529
rs73607583	snp	C/G	0.104859	0.203554	intron-variant	NEBL	GRCh38.p7	10:21048307	AAGGAGAGTCACAGA[C/G]CCACAGCATGCTGGG	10529
rs73607584	snp	A/G	0.00993419	0.0697739	intron-variant	NEBL	GRCh38.p7	10:21052156	CCAAGAAGTGTTTGC[A/G]CTTTTTCCTTCAGAA	10529
rs73607586	snp	C/T	0.271162	0.249103	intron-variant	NEBL	GRCh38.p7	10:21078586	AGTTTTTATAAATGA[C/T]CTGTATACACGTATG	10529
rs73607587	snp	C/G	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:21083880	AGCTACACTCTTACA[C/G]GTCTGCCTATGACTG	10529
rs73607588	snp	A/G	0.270892	0.249126	intron-variant	NEBL	GRCh38.p7	10:21090482	GCGTGTAGGTTATAT[A/G]AAAACACTTTGCCAT	10529
rs73607589	snp	A/G	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:21093746	CTGGAAGAGGAGAAC[A/G]ATATTTTATCCTGAA	10529
rs73607590	snp	A/G	0.00438332	0.0466095	intron-variant	NEBL	GRCh38.p7	10:21099148	TAAAAATAAAAATAA[A/G]ATCAAAACAGAGTGA	10529
rs73607591	snp	C/G	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:21102153	AGACTTCTACCACAA[C/G]TGTTAATAAGCTACT	10529
rs73607593	snp	A/G	0.136166	0.22258	intron-variant	NEBL	GRCh38.p7	10:21114420	GAGATAGGACGTTCT[A/G]TAAATGTCAATTTGA	10529
rs73607594	snp	C/T	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:21120618	TAAAATACCGGTTCT[C/T]TCTCCCATCATCCTT	10529
rs73607595	snp	C/T	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:21121539	TCAATGTATGCCTAT[C/T]ACGTGCACACTATAT	10529
rs73607596	snp	A/G	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:21122523	ATCTACTCACAATCC[A/G]GAATAAGTGGCCATG	10529
rs73607597	snp	C/T	0.00636936	0.0560724	intron-variant	NEBL	GRCh38.p7	10:21122776	TAGCAGTTGAAAATA[C/T]GACAGATCAATTTCC	10529
rs73607598	snp	C/T	0.00438332	0.0466095	intron-variant	NEBL	GRCh38.p7	10:21124344	TTATTAATGCAGGAA[C/T]GAAAAGAAATCCAAT	10529
rs73607599	snp	C/T	0.118933	0.212888	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21125479	ATTTAAGGCTTCCCT[C/T]GAAATCTAGCATCAT	10529
rs73607600	snp	A/C	0.0341408	0.126114	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21128812	TAACATTGAAAAAAA[A/C]CAGAAAAGATGGTCC	10529
rs73607601	snp	C/T	0.0700422	0.173537	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21130071	AAGATATCATGATAA[C/T]ACTAACCAAAAGAAA	10529
rs73607602	snp	A/G	0.0980852	0.198549	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21131223	AAGAAGCCCATATCT[A/G]TTCAAGAAATTGGAT	10529
rs73609203	snp	C/T	0.0704125	0.17392	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21132433	AGCTGTTATGCATAA[C/T]GCTTCTGTGAACATT	10529
rs73609204	snp	G/T	0.0607341	0.163335	intron-variant	NEBL	GRCh38.p7	10:21153878	TTTACATCTTAAAAG[G/T]TAAGATGTAGGACCT	10529
rs73609206	snp	C/T	0.0777841	0.181223	intron-variant	NEBL	GRCh38.p7	10:21157718	CTGTTGGAGTTGAAT[C/T]GTATATGTATTGGAG	10529
rs73609207	snp	A/G	0.077417	0.180873	intron-variant	NEBL	GRCh38.p7	10:21158369	CAGTGTCTACTCTAT[A/G]TCAACTATTTACATA	10529
rs73609208	snp	C/T	0.0777841	0.181223	intron-variant	NEBL	GRCh38.p7	10:21158437	AGCAAATACTATTAT[C/T]ATCAGCAACTGAGAC	10529
rs73609209	snp	A/G	0.0659589	0.169201	intron-variant	NEBL	GRCh38.p7	10:21162649	CTCCAGGCTGAGAAT[A/G]TCTATGGTCCAATTT	10529
rs73609210	snp	C/T	0.0770498	0.180522	intron-variant	NEBL	GRCh38.p7	10:21162997	CTGCTAAGCTCATTA[C/T]TAGATTGGATATTCC	10529
rs73609211	snp	C/T	0.0770498	0.180522	intron-variant	NEBL	GRCh38.p7	10:21163628	ATTTCTCCAAGTTCT[C/T]TGTGTTTGGTTGCAC	10529
rs73609212	snp	C/T	0.114387	0.210022	intron-variant	NEBL	GRCh38.p7	10:21163970	AACAATCATTGCCAC[C/T]TAAACCTGGTCCTTC	10529
rs73609213	snp	A/G	0.0905309	0.192535	intron-variant	NEBL	GRCh38.p7	10:21167042	GAGAGGCAGCGGAGC[A/G]CTGGCCTCGATAATC	10529
rs73609214	snp	C/T	0.0633504	0.166319	intron-variant	NEBL	GRCh38.p7	10:21167362	CATTTGACTAAGATA[C/T]AAGGTATAGTAAATG	10529
rs73609215	snp	C/T	0.0652144	0.168387	intron-variant	NEBL	GRCh38.p7	10:21169471	GATTGACATGCACCA[C/T]GTGAATTAGAGCCAA	10529
rs73609216	snp	G/T	0.0535932	0.154675	intron-variant	NEBL	GRCh38.p7	10:21169905	AGTATTAAAAATAAG[G/T]TTAAGACCTATGAAA	10529
rs73609217	snp	A/G	0.0711525	0.174681	intron-variant	NEBL	GRCh38.p7	10:21169946	GGATGTTTCTTTTTC[A/G]TAAGTAGAATCATTT	10529
rs73609218	snp	C/T	0.0115144	0.0749975	upstream-variant-2KB, intron-variant	NEBL, NEBL-AS1	GRCh38.p7	10:21174478	TCCCTCTTCTCTTCC[C/T]CAGCCGGGGGCACCC	10529
rs73609219	snp	A/G	0.0872718	0.189788	upstream-variant-2KB, intron-variant	NEBL, NEBL-AS1	GRCh38.p7	10:21174979	CACCGCAAAGATCTG[A/G]GAAAAGTTCTTCACC	10529
rs73609220	snp	C/T	0.0607341	0.163335	upstream-variant-2KB, intron-variant	NEBL, NEBL-AS1	GRCh38.p7	10:21175287	GCAGCTACCGAACAG[C/T]TTCTACTCTCCTGCT	10529
rs73609221	snp	C/G	0.0678174	0.1712	upstream-variant-2KB	NEBL	GRCh38.p7	10:21175661	CCAAATTCAACAGCC[C/G]CTGAGCCACTCACTC	10529
rs74120503	snp	A/G	0.0189856	0.0955633	intron-variant	NEBL	GRCh38.p7	10:20893606	TCTATGGAGAATTCT[A/G]AGCAGTGCAGGCTTC	10529
rs74120504	snp	C/T	0.0376037	0.131863	intron-variant	NEBL	GRCh38.p7	10:20895031	TAAACAGAAAGTATG[C/T]CTATCTGTTTCATTT	10529
rs74120507	snp	C/T	0.0901694	0.192235	intron-variant	NEBL	GRCh38.p7	10:20901655	TCTTATTATAAAATA[C/T]TCATTCCAAATGGTT	10529
rs74120518	snp	A/G	0.0475351	0.146656	intron-variant	NEBL	GRCh38.p7	10:20905716	AAGAGCATTTGCAAA[A/G]ACCCAGAGACAAGAG	10529
rs74120522	snp	C/T	0.0232847	0.105357	intron-variant	NEBL	GRCh38.p7	10:20911789	GAAATTAAATTCTGA[C/T]AGAGCCAAGAGTATG	10529
rs74120524	snp	A/G	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20913564	AATGAAAAAATGTTC[A/G]GTTTACTGGAAATAG	10529
rs74120525	snp	C/T	0.14933	0.228835	intron-variant	NEBL	GRCh38.p7	10:20914597	TCCTCAAGTCTATTT[C/T]GGTAGTTTATATATT	10529
rs74120528	snp	A/G	0.0391387	0.134304	intron-variant	NEBL	GRCh38.p7	10:20927192	AATGAAGAAGAATAA[A/G]AGGAATGGACCATGA	10529
rs74120532	snp	A/G	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:20930782	TTCTAATCCTCTTTT[A/G]CCACACAGGAGCATG	10529
rs74120534	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20935406	ATTATCAGCATCTCT[G/T]CATCGAATTCACTAA	10529
rs74120536	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20935510	TAAAATATTTGCATC[A/G]CCTGGAAATCACACG	10529
rs74120565	snp	C/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20936849	TATGAATAAGCTTGG[C/G]TCGATTCCTTTTCAG	10529
rs74120566	snp	G/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20937304	TCTGAGTCACGCAAA[G/T]GGCTTTTCCATCATG	10529
rs74120567	snp	A/C/G	0.0174175	0.0916809	intron-variant	NEBL	GRCh38.p7	10:20949761	TTTTCTGCTGAGGAC[A/C/G]TCTTTATTTCCTTAT	10529
rs74120573	snp	C/T	0.0337553	0.125452	intron-variant	NEBL	GRCh38.p7	10:20963039	ACACACACACACACA[C/T]ACACACACGGAAATC	10529
rs74120574	snp	A/C	0.0562307	0.157967	intron-variant	NEBL	GRCh38.p7	10:20965100	AAGAGCATTGCTTTC[A/C]TGGACAATCCTTTGC	10529
rs74120575	snp	A/G	0.0345262	0.126772	intron-variant	NEBL	GRCh38.p7	10:20966303	CTAAAGCAAGAATCA[A/G]GAAACCTGAATTTAA	10529
rs74120576	snp	C/T	0.0799831	0.183287	intron-variant	NEBL	GRCh38.p7	10:20967164	ACATGTTCTTAATAA[C/T]GTTGTTTCTATTTTC	10529
rs74120584	snp	A/T	0.0325976	0.123435	intron-variant	NEBL	GRCh38.p7	10:20980398	AGAAAAAGAAAAAAA[A/T]ATATATTTAGGTGCT	10529
rs74120585	snp	C/T	0.00914312	0.0669923	intron-variant	NEBL	GRCh38.p7	10:20981728	CTTCCACTGGACTGA[C/T]AGCTACAAGGATGTA	10529
rs74120586	snp	C/G	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:20981814	AGTTGTCACAGAAGA[C/G]ATGAATTGAGAGATA	10529
rs74120588	snp	C/T	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:20987516	CTCACTCCTCAATCC[C/T]TAACCCCCTCTCCCA	10529
rs74120589	snp	C/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20992571	GACCTCTTATCAGCA[C/G]ATTTAATAGGGTCCT	10529
rs74120592	snp	C/T	0.031825	0.122064	intron-variant	NEBL	GRCh38.p7	10:20995798	CTCTGCAGATGCTGC[C/T]CGGCTTGAAAATAAT	10529
rs74120597	snp	A/G	0.0391387	0.134304	intron-variant	NEBL	GRCh38.p7	10:21006502	CCGTGAGACCTGTAA[A/G]TCCAACCAGTCCTTC	10529
rs74120599	snp	A/G	0.039522	0.134904	intron-variant	NEBL	GRCh38.p7	10:21006770	GATATTGTTTACGAC[A/G]TGATTTAATTTTGCC	10529
rs74120602	snp	C/T	0.0391387	0.134304	intron-variant	NEBL	GRCh38.p7	10:21010178	AGATCAGCTCCTCTG[C/T]ATAAGGGATCACAGA	10529
rs74120659	snp	C/T	0.110519	0.207473	intron-variant	NEBL	GRCh38.p7	10:20794241	GGAGGAAGTGTACAG[C/T]CTAAAATATCTTTGC	10529
rs74120660	snp	C/T	0.0193772	0.0965046	intron-variant	NEBL	GRCh38.p7	10:20794268	TTGCAAAATCAAAAA[C/T]CCTCTCTCAAGCCAA	10529
rs74120663	snp	A/T	0.0854556	0.188216	intron-variant	NEBL	GRCh38.p7	10:20796464	CACAACATTAGTTGT[A/T]TTTTTAATTTTCCAC	10529
rs74120665	snp	C/T	0.0618563	0.164627	intron-variant	NEBL	GRCh38.p7	10:20798756	ATTTTTAATGTTGTA[C/T]TGTTTCTAGTTTAAG	10529
rs74120667	snp	A/G	0.00591954	0.0540808	intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20817691	TCTCCCTTATATTTT[A/G]CCTAAGAAGGATAAA	10529
rs74120668	snp	G/T	0.084728	0.187577	intron-variant	NEBL	GRCh38.p7	10:20822929	TTTCACCTCTCATCC[G/T]GCTCTCACCCTCCTA	10529
rs74120683	snp	C/T	0.0551013	0.156571	intron-variant	NEBL	GRCh38.p7	10:20823989	CTACTTCACTCAAAA[C/T]CTCCCCCATCACATA	10529
rs74120684	snp	C/T	0.0547245	0.156101	intron-variant	NEBL	GRCh38.p7	10:20824971	CATCTACCAGGCTAA[C/T]ACAGGCTCTCACCAT	10529
rs74120685	snp	C/G	0.107341	0.205301	intron-variant	NEBL	GRCh38.p7	10:20825034	ATCCACACCTTAAGC[C/G]TAGGTCCTCCTTACA	10529
rs74120687	snp	A/G	0.0111196	0.0737302	intron-variant	NEBL	GRCh38.p7	10:20829053	CTAAATACTTAACAC[A/G]CACTAACTCATTTAA	10529
rs74120689	snp	A/G	0.196149	0.244131	intron-variant	NEBL	GRCh38.p7	10:20830619	GCCACTGTTAGCTTT[A/G]TTTGGAACTATTTTA	10529
rs74120694	snp	A/G	0.0509478	0.151255	intron-variant	NEBL	GRCh38.p7	10:20834664	TCCACTGAAGCCCCC[A/G]CCTAACCAACCTTGA	10529
rs74120695	snp	A/G	0.0429648	0.14013	intron-variant	NEBL	GRCh38.p7	10:20835833	GCATGCAAAGCTCCA[A/G]AAATGTTTAGTATAC	10529
rs74120696	snp	A/G	0.115088	0.210473	intron-variant	NEBL	GRCh38.p7	10:20838853	AGCACTATTATAAAT[A/G]AAGTACTTTAAATTA	10529
rs74120697	snp	C/T	0.0433465	0.140692	intron-variant	NEBL	GRCh38.p7	10:20843219	CAGTACAAAGGTGTC[C/T]GCAAGCCGGTAAGAG	10529
rs74120698	snp	A/G	0.0433465	0.140692	intron-variant, upstream-variant-2KB	NEBL, LOC102725112	GRCh38.p7	10:20843902	CCATATTCACCTTAC[A/G]GTGCTGCAGAACACC	10529
rs74120699	snp	A/G	0.0551013	0.156571	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20846083	ACCATTAGCCTTTTT[A/G]AAACACTGAGCCACT	10529
rs74120700	snp	A/G	0.113685	0.209567	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20846291	ATCCCTGAAATGATA[A/G]AAGTAAATAAATTCT	10529
rs74120701	snp	A/G	0.0551013	0.156571	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20846677	TCTAGGGCATCTCTA[A/G]GCTAAAAAGGACTCT	10529
rs74120702	snp	C/T	0.0551013	0.156571	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20847238	CTGGCCTTTAGCATA[C/T]GAATTGGGTCCAAAG	10529
rs74121007	snp	C/T	0.0633504	0.166319	intron-variant	NEBL	GRCh38.p7	10:21074447	ACATCTCTTGTAAAA[C/T]GCTGCTCCTCATTGA	10529
rs74121008	snp	A/G	0.0263992	0.111815	intron-variant	NEBL	GRCh38.p7	10:21080187	TAAAGTAATGAAAGC[A/G]ATTTCTTAACAGCAC	10529
rs74121019	snp	C/T	0.0387552	0.1337	intron-variant	NEBL	GRCh38.p7	10:21093310	CAGAAGCATTGGACG[C/T]ATTTTATCATAGGAC	10529
rs74121021	snp	A/T	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21105026	ATGGAAAACATTGAT[A/T]GATCTTTTTTAAGGT	10529
rs74121023	snp	A/G	0.0383715	0.133092	intron-variant	NEBL	GRCh38.p7	10:21119959	TTGCGGATTTATCTA[A/G]TTGTTTCCTCATGAT	10529
rs74121025	snp	A/C	0.0387552	0.1337	intron-variant	NEBL	GRCh38.p7	10:21121243	GCTTATGGAGAGACA[A/C]CCTGAGCCCTTAACA	10529
rs74121026	snp	C/T	0.0566069	0.158427	intron-variant	NEBL	GRCh38.p7	10:21123101	ACAATGAAGACTGCC[C/T]TCTACAGGTGGCCTG	10529
rs74121053	snp	A/G	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21134744	AATATAATTAGATGG[A/G]GAAACCTTCTGGGAT	10529
rs74121055	snp	C/T	0.0298908	0.118541	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21139132	AGATGTTAAGAGTCA[C/T]GGCTGGCCTAGGAAT	10529
rs74121073	snp	C/T	0.0236746	0.106192	intron-variant	NEBL	GRCh38.p7	10:21160900	ATGCAAGTAAATGTG[C/T]ATATGGTCTGATGTC	10529
rs74121075	snp	A/G	0.0901694	0.192235	intron-variant	NEBL	GRCh38.p7	10:21161603	TTATATTAAGAATCC[A/G]CCCATAATTAGTGAC	10529
rs74121076	snp	A/C	0.0134861	0.0810011	intron-variant	NEBL	GRCh38.p7	10:21163573	TAACTCCCGCTCCAC[A/C]TCCCAGATCTATAGA	10529
rs74121084	snp	C/G/T	0.0146672	0.084371	intron-variant	NEBL	GRCh38.p7	10:21170684	TTCTGTTCAATGCCC[C/G/T]CATTTTCTGATTTCT	10529
rs74122503	snp	A/G	0.0441095	0.141807	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20847723	AGGAAAGTGATTTTT[A/G]ATCCCTGTCTCTTTC	10529
rs74122603	snp	C/G	0.0391387	0.134304	intron-variant	NEBL	GRCh38.p7	10:21014601	AAGATGCAACTCCCC[C/G]CTGAGAAAGGTTCTG	10529
rs74122604	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21015465	GGGAATGCTTTCTAC[C/T]ACATGATATTAAAAT	10529
rs74122605	snp	C/G	0.0391387	0.134304	intron-variant	NEBL	GRCh38.p7	10:21016073	GGGCTGCTGCGGGCC[C/G]GTGGGGGCGTCTAAC	10529
rs74122607	snp	C/T	0.103082	0.202275	intron-variant	NEBL	GRCh38.p7	10:21029459	CCCTGCTCAGTGCCC[C/T]GAGTCTCAATTAAGA	10529
rs74122609	snp	C/T	0.0103295	0.0711199	intron-variant	NEBL	GRCh38.p7	10:21038155	AAAAGCATGACATTT[C/T]CAATCAAGTAGCAAC	10529
rs74122610	snp	A/T	0.00953873	0.0683987	intron-variant	NEBL	GRCh38.p7	10:21041434	CATCATCATCACCAC[A/T]AACAACCAAGGGAAG	10529
rs74122613	snp	C/T	0.00953873	0.0683987	intron-variant	NEBL	GRCh38.p7	10:21047252	AGTAACAGACACTGA[C/T]TATGGTCATGAATAA	10529
rs74122615	snp	G/T	0.00953873	0.0683987	intron-variant	NEBL	GRCh38.p7	10:21050865	GCTCTCTGTCTCCAG[G/T]ACACAGCACTGTTTC	10529
rs74122629	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21060402	CCTAGAGATTACCTG[A/G]AATGGTGGTTCTCAA	10529
rs74123503	snp	A/G	0.162581	0.234218	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20848265	CAGTGTTTACAAACT[A/G]TTATCTAAAGGAAGA	10529
rs74123506	snp	A/G	0.162253	0.234095	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20849107	AGACCAGCATCCACT[A/G]TTTCTATCCCTTTGC	10529
rs74123508	snp	A/T	0.112631	0.208878	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20861027	ACTGATTTTAAGTAA[A/T]CAGCAAGAACTCTTT	10529
rs74123509	snp	C/G	0.0444908	0.142359	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20861605	GTGGACTCTTCAACA[C/G]CCTTCCGCTGGAATG	10529
rs74123510	snp	A/G	0.141687	0.225598	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20867248	ATTAACTTTGAAAGA[A/G]TTAACATTTTTTAGG	10529
rs74123511	snp	C/T	0.100588	0.200439	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20874341	CTGCCAGATACCCCA[C/T]CCATTTGGAAACCAT	10529
rs74123513	snp	C/T	0.0952156	0.196321	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20879468	TATGTTAGAAAAGTG[C/T]TCTGCTTTTGGCATA	10529
rs74123514	snp	A/T	0.0952156	0.196321	intron-variant, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20879637	TCAGCCAAGCACCAT[A/T]CCATAAAGGGACTAA	10529
rs74123530	snp	C/G	0.0456336	0.143994	intron-variant, splice-acceptor-variant	NEBL, LOC102725112	GRCh38.p7	10:20884649	ATTTTATATGACACA[C/G]GTAAATGTGCTGTTA	10529
rs74123531	snp	C/T	0.117886	0.21224	intron-variant	NEBL	GRCh38.p7	10:20886088	TTAATACCTAGGGGA[C/T]GGGTTCATATTAAAT	10529
rs74123532	snp	C/T	0.093417	0.194889	intron-variant	NEBL	GRCh38.p7	10:20887210	ATTACTCCTAAACCC[C/T]TCTGGATTCAAAATG	10529
rs74123533	snp	G/T	0.0930568	0.194599	intron-variant	NEBL	GRCh38.p7	10:20887213	ACTCCTAAACCCTTC[G/T]GGATTCAAAATGAGT	10529
rs74123535	snp	A/T	0.0356815	0.128715	intron-variant	NEBL	GRCh38.p7	10:20890019	CCTTTTTTGAATGAT[A/T]ATTAGGTTGATAAAG	10529
rs74194246	snp	A/G	0.0150606	0.0854603	intron-variant	NEBL	GRCh38.p7	10:20909232	GCTATCAAATAGTAG[A/G]TTTCGTTCATTCTAT	10529
rs74229939	snp	G/T	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:20819941	TCCTTCAGATTATAT[G/T]ATTTATTGGTGGCCT	10529
rs74229943	snp	C/T	0.0232847	0.105357	intron-variant	NEBL	GRCh38.p7	10:20896392	TCACAACAAAAATAC[C/T]CCTTGCACTAATATC	10529
rs74229945	snp	C/T	0.0240643	0.107019	intron-variant	NEBL	GRCh38.p7	10:20918564	AATAAATGCATAATA[C/T]TGGGGCCGGGCACGG	10529
rs74229950	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20980065	ACAAAAAAAAAAAAA[A/C]AAACCATAAAATTCA	10529
rs74261069	in-del	-/AA			intron-variant	NEBL	GRCh38.p7	10:20967193	TCAAAGAAAAAAAAA[-/AA]TAGGAAACAACCTAA	10529
rs74326867	snp	G/T	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20826623	AAAGACAATTTCTCA[G/T]GTTTTATAATAATAT	10529
rs74333822	snp	A/G	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:20981697	AGACCCACTGACACC[A/G]GTGATAGGGGCCTCT	10529
rs74336381	snp	C/T	0.0178098	0.0926698	intron-variant	NEBL	GRCh38.p7	10:20930297	AAACATTTCATCCTT[C/T]GACACGTTTTATTGG	10529
rs74338502	snp	C/G	0.5	0	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20872220	CTTTGAATAGGGCCC[C/G]ATCATCCATGTAAAT	10529
rs74379842	snp	A/T	0.0232847	0.105357	intron-variant	NEBL	GRCh38.p7	10:21015302	ACGGTAGCTCCATGT[A/T]GTTGTCTTCTCAGTA	10529
rs74405548	snp	A/C	0.084364	0.187256	intron-variant	NEBL	GRCh38.p7	10:21150987	GGAAAATTAATGACC[A/C]CCACTCAGAAATATA	10529
rs74409520	snp	C/T	0.0236746	0.106192	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20849847	GGATACAGAATTTCA[C/T]CTAAGACAATTTCAG	10529
rs74415341	snp	C/T	0.0205511	0.0992634	intron-variant	NEBL	GRCh38.p7	10:20935845	TCAATACATGAGAAT[C/T]ATTATAGGCCCAACT	10529
rs74415627	snp	G/T	0.0726307	0.176182	intron-variant	NEBL	GRCh38.p7	10:21055432	CAGATCTTTTAACTT[G/T]GGTGTCAATGCTGTA	10529
rs74416827	snp	A/C	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:21019398	CCTTCTCCCCTCTTC[A/C]GTCCTTACTTCACCA	10529
rs74461164	snp	A/G	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21067981	ATGCCGTCTCAAAGA[A/G]AAAAAAATGTAATAT	10529
rs74463331	snp	G/T	0.0733688	0.176922	intron-variant	NEBL	GRCh38.p7	10:20838934	AGTATGGTATAAACA[G/T]AACATGTATATGTAT	10529
rs74478440	snp	A/G	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21034192	AAAAAAAAAAAAAAG[A/G]CCCAAACAAAACTAG	10529
rs74479831	snp	C/G	0.0252325	0.109451	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21141921	ACTCCACCTCCCACG[C/G]CTTCAGCAGAACTCC	10529
rs74500083	snp	C/T	0.0240643	0.107019	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20870239	GCTGAGGAAGGAAAA[C/T]CGCTCAAACCCGAGA	10529
rs74511201	snp	C/T	0	0	intron-variant	NEBL	GRCh38.p7	10:20912884	AGTATGCCAATTCTT[C/T]TTTTTTTTTTTTTTT	10529
rs74516804	snp	C/G	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:21152110	TGCATTTCCGCTATC[C/G]GGAAATGGGACAGAG	10529
rs74571893	snp	A/C	0.0547245	0.156101	intron-variant	NEBL	GRCh38.p7	10:21010049	GAGACAGTAGTGTCT[A/C]AGTAGTGTCCTCCTT	10529
rs74577799	snp	A/G	0.0287284	0.116357	intron-variant	NEBL	GRCh38.p7	10:20800680	CTCTTCTGCATAAAC[A/G]ACAAATGCTCACAAT	10529
rs74603047	snp	C/T	0.084364	0.187256	intron-variant	NEBL	GRCh38.p7	10:21071718	GCCATAAAGAATTAC[C/T]ATAAATTTGGTGGCT	10529
rs74612862	snp	A/G	0.00478085	0.0486577	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20958369	CAGTTGTGAAAATCC[A/G]TAAGGCAGGGCTTTC	10529
rs74619267	snp	C/G	0.0678174	0.1712	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20860999	AATTTCTGATATTCT[C/G]AATACCTTACAAACT	10529
rs74620590	snp	A/T	0.0482946	0.147699	intron-variant	NEBL	GRCh38.p7	10:21084608	TCCCAAAAAAAAAAT[A/T]AAAAAATAAAAATAA	10529
rs74621501	snp	C/T	0.0260105	0.111035	intron-variant	NEBL	GRCh38.p7	10:21118278	AACATGGTTTTCTTC[C/T]AGTCAGGATCAAAGT	10529
rs74658699	snp	C/T	0.0356815	0.128715	intron-variant	NEBL	GRCh38.p7	10:20904618	AGGTGGGGTCTCATT[C/T]GACTACTGGCAAATG	10529
rs74689835	snp	A/C	0.0119091	0.0762411	upstream-variant-2KB	NEBL	GRCh38.p7	10:21176129	CGTCTCAGTCTCCTG[A/C]GTACCTGCGACCACA	10529
rs74693012	snp	A/G	0.0146672	0.084371	intron-variant	NEBL	GRCh38.p7	10:20931128	TAAGAAAAAAAAAAT[A/G]AACTCTCTAGCATTT	10529
rs74697606	snp	A/C	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:20963729	GAGCTGACTACTGTT[A/C]AACAATCCTTTCCAC	10529
rs74704549	snp	A/G	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:21055582	CCAGCTATGCCACTT[A/G]GGGATGTTATTTAAC	10529
rs74707828	snp	C/T	0.0448719	0.142907	intron-variant	NEBL	GRCh38.p7	10:21095001	TGCCTATATCCATAG[C/T]AGTGTATTCAAAATC	10529
rs74721974	snp	A/T	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20969186	TTTTTAAGGTGAAGT[A/T]AATTTTAGCAAATGT	10529
rs74735085	snp	A/G	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20981318	AAAGAAAAAAAAAAA[A/G]GACATTCTAATGTTG	10529
rs74755162	snp	C/T	0.0178098	0.0926698	intron-variant	NEBL	GRCh38.p7	10:21093584	ACAGGAGAAAGAATA[C/T]GCAACCAGATGGGGG	10529
rs74758473	snp	A/C/G	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20836298	CGTGATCTCGGCTCA[A/C/G]TGCAACTTGTGCCTC	10529
rs74758826	snp	A/G	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:20911646	TATAAATAAGAAAGT[A/G]TAAGTGGATTTTATA	10529
rs74761701	snp	G/T	0.0126979	0.078662	intron-variant	NEBL	GRCh38.p7	10:20827414	ATCTGACCAGCTTAC[G/T]CTGAGAGCTGGCGCT	10529
rs74782690	snp	A/C	0.0460142	0.144533	intron-variant	NEBL	GRCh38.p7	10:21150068	TATTATTGACTTCTA[A/C]ACTAAATAAAGGCTC	10529
rs74791548	snp	C/G	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21078053	TATTCTGAAAGCTGG[C/G]TTGTGTGCAGAATGG	10529
rs74802570	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20981603	ATAACATGACTTGGG[A/G]CTGGCTAATCAGAGT	10529
rs74807419	snp	C/G	0.00557542	0.0525036	intron-variant	NEBL	GRCh38.p7	10:21051164	TCAACCTCAACCTGA[C/G]TATGACCACATCATA	10529
rs74808940	snp	A/C	0.0244538	0.107838	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20853913	CCTAACAGAAAGAAA[A/C]GACAAATGCTTGAAC	10529
rs74812452	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20798110	CCCTGTTTCTAATTA[A/C]AAAAAAAAAAAAAAA	10529
rs74822947	snp	A/G	0.0733688	0.176922	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20882169	AAGATCCTGCAAAAG[A/G]AAGAAAGAAGGAAAG	10529
rs74840848	snp	A/G	0.0429648	0.14013	intron-variant	NEBL	GRCh38.p7	10:21086392	CTATAGCTGCTCCCT[A/G]TAGGTTTCCTCTCAA	10529
rs74865003	snp	A/G	0.0475351	0.146656	intron-variant	NEBL	GRCh38.p7	10:21116536	GTAAAGATGAGGAGG[A/G]TCACAATTCAGTCCA	10529
rs74870833	snp	C/G	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20968621	AGAACTATGCAAGGA[C/G]GGAAGGTATATATAG	10529
rs74873818	snp	A/C	0.0425829	0.139564	intron-variant	NEBL	GRCh38.p7	10:21088489	ATTCTGTCTCTTAAA[A/C]AACAAAACAAAACCT	10529
rs74877699	snp	A/G	0.5	0	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20959795	TTTTTTTTTTAAAAA[A/G]AGATGTTGTCTAAGT	10529
rs74888649	snp	A/G	0.0539704	0.155153	intron-variant	NEBL	GRCh38.p7	10:21158353	ATAGCCAACATTTAT[A/G]CAGTGTCTACTCTAT	10529
rs74896090	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20965722	GCAAACTCCTTGGAA[C/G]TGTGCAGGACAGACG	10529
rs74898268	snp	C/T	0.0142736	0.0832652	intron-variant	NEBL	GRCh38.p7	10:21087030	TCTCTTAACCTACCA[C/T]CCTCCCTCACCAAGA	10529
rs74914676	snp	A/G	0.5	0	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20781969	AGTTCATCTTGTGTA[A/G]TGAATCCAGCCTCAC	10529
rs74941965	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:20818452	GAGTAGCGCTGCCTT[C/G]TTAACTATTTTTGCT	10529
rs74943054	snp	A/G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20835703	GATACTAAAAAAAAA[A/G/T]TAGTTAGACATATTT	10529
rs74960967	snp	C/G	0.0399052	0.1355	intron-variant, utr-variant-5-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20897371	TTATCTCAGTGGTGT[C/G]TGAGTGAACAGAAAA	10529
rs74965982	in-del	-/T	0.226779	0.248919	intron-variant	NEBL	GRCh38.p7	10:20807667	TGCTCAACCTCAAAA[-/T]TTCCTACCTTTGGGA	10529
rs74977492	snp	G/T	0.0248432	0.108648	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20878457	TAAATTCTCTGCAAT[G/T]AGTTTCATTTGGCTG	10529
rs74982127	snp	A/G	0.00951936	0.0683305	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21126207	ACATTTGGAATAATA[A/G]CAACTACATTGCTGG	10529
rs74991364	snp	A/T	0.206947	0.246265	intron-variant	NEBL	GRCh38.p7	10:20903485	AACTAAAAGTAGAGC[A/T]ACCATAGGATTCAGC	10529
rs74993384	snp	C/G	0.077417	0.180873	intron-variant	NEBL	GRCh38.p7	10:21066555	TTAACTAAAGGAAAA[C/G]AAGACTGATCCAGAA	10529
rs74994550	snp	C/T	0.02016	0.0983543	intron-variant	NEBL	GRCh38.p7	10:21098772	CTGGCCAGCTTTCCC[C/T]CATGGCCTCTCACTT	10529
rs75001682	snp	A/G	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20948861	TCCCAGTGGTTTGTC[A/G]TTAACACAGACTGGG	10529
rs75003365	snp	A/C	0.375	0.216506	intron-variant	NEBL	GRCh38.p7	10:21040869	GCAGGAAGAAGAGAA[A/C]GCTAAGGGGGAGGTG	10529
rs75017280	snp	C/T	0.0228947	0.104514	intron-variant	NEBL	GRCh38.p7	10:20841409	CTCACCACAGCCTGA[C/T]AGATGGTACTTGAAA	10529
rs75021525	snp	C/T	0.00953873	0.0683987	intron-variant	NEBL	GRCh38.p7	10:21025198	CACATTCATAAGTTT[C/T]ATGGAAAACAAAACA	10529
rs75032915	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21045767	CATTGTTGATGAAAA[C/T]GTAAATTAGTATAGC	10529
rs75051967	snp	A/G	0.0547245	0.156101	intron-variant	NEBL	GRCh38.p7	10:21161546	GAATGTAATTTGCCA[A/G]TAGGACAGACTCGTG	10529
rs75064947	snp	C/T	0.0236746	0.106192	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20851804	AAAAATTTTGTGAAA[C/T]AAATGAAATGAAAAT	10529
rs75065776	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21033753	TCCGAAAAAAAAAAA[A/G]AAAGAAAGAAAAGAA	10529
rs75067084	snp	C/T	0.0652144	0.168387	intron-variant	NEBL	GRCh38.p7	10:20956597	GACTTACAATAAAAA[C/T]AACATTCATTCTCCC	10529
rs75074306	snp	G/T	0.0372196	0.131242	intron-variant	NEBL	GRCh38.p7	10:21006779	TACGACATGATTTAA[G/T]TTTGCCAAGGATAAC	10529
rs75082340	in-del	-/AA			downstream-variant-500B	NEBL	GRCh38.p7	10:20779581	ATGAAGAAAAAAAAA[-/AA]TCCCCTTTTACCTAC	10529
rs75098478	snp	C/T	0.0240643	0.107019	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20866559	ACAACTATATCCTCT[C/T]GCCCAGAGGCTCTGC	10529
rs75103346	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20935532	AATCACACGGACTTT[A/G]GCAGATCTCCTCCTT	10529
rs75106452	snp	A/C	0.0185938	0.0946107	intron-variant	NEBL	GRCh38.p7	10:21046365	AATTGCTAGGAAAAT[A/C]GATTTTGTAGTGTTA	10529
rs75123427	snp	C/T	0.00676609	0.0577691	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20845902	TTAATGATTTTGGAG[C/T]TGAGAATATTTCTCT	10529
rs75131703	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20825183	CACTTTCTTCACAAA[C/T]GCTGACCCACACTGA	10529
rs75137269	snp	A/G	0.0926964	0.194308	intron-variant	NEBL	GRCh38.p7	10:20805130	GAGTGAAAGACAAGC[A/G]TCAGGGATGACTCCA	10529
rs75158109	snp	C/G	0.0329836	0.124112	intron-variant	NEBL	GRCh38.p7	10:21016377	ATAGATTCCAAAAAA[C/G]CTTGAGAGGATTTAG	10529
rs75162597	snp	A/G	0.0372196	0.131242	intron-variant	NEBL	GRCh38.p7	10:21006601	GATGGAGTTCACTAT[A/G]CCCTGAACTTCTGCA	10529
rs75167492	in-del	-/AAGT			intron-variant	NEBL	GRCh38.p7	10:21073636	AAAAAAAAAAAAAAA[-/AAGT]CTTTATTTCAATCAT	10529
rs75170688	snp	A/C	0.0418818	0.138851	intron-variant	NEBL	GRCh38.p7	10:20992660	TAGCTCTCCTACCCT[A/C]GCCTTGAGCTGCCTT	10529
rs75197968	snp	A/G	0	0	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20850015	TGAAAAAAAAAGGGG[A/G]CCAGGTAAATAAAGC	10529
rs75209953	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20890194	GCATCAACACCAGGC[A/G]TGCTGGCTACGGGTG	10529
rs75218895	snp	A/C	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20991348	AGTTTGAAAATTTTT[A/C]TGACAGTGTTATAAA	10529
rs75237567	snp	C/T	0.0345262	0.126772	intron-variant	NEBL	GRCh38.p7	10:21036949	TGCTTTTGTTTGTTT[C/T]GTTTTGTTTATTCCA	10529
rs75247952	snp	A/G	0.0185938	0.0946107	intron-variant	NEBL	GRCh38.p7	10:21001050	CCTCAGGAAACCAAT[A/G]CAGGTCCCCATGAGC	10529
rs75248234	snp	A/C	0.0505692	0.150756	intron-variant	NEBL	GRCh38.p7	10:20824010	CCATCACATATATTT[A/C]GAGGAAGATCAATCA	10529
rs75251494	snp	A/C	0.0244538	0.107838	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20862756	TTAAGACACAATGTT[A/C]CTCCTTATACCTACA	10529
rs75259436	snp	C/G	0.0275645	0.114116	intron-variant	NEBL	GRCh38.p7	10:20802491	CAAACCCTTTGGTAA[C/G]TTAATACATTGAAAA	10529
rs75275670	snp	C/T	0.00438332	0.0466095	intron-variant	NEBL	GRCh38.p7	10:21115581	TGCTCCATTGTCTTC[C/T]GACTTGCATTGTTTC	10529
rs75301590	snp	C/G/T	0.000313407	0.0125144	intron-variant, synonymous-codon, missense, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20869761	TATGATCTTAGAGAT[C/G/T]TGGGTTGCCATCTTG	10529
rs75319006	snp	C/T	0.0752113	0.178743	intron-variant	NEBL	GRCh38.p7	10:21090758	GTCATTAGCCAGTTT[C/T]CTCCTGGCTCAGAAG	10529
rs75324054	snp	A/C/T	6.61139e-05	0.00574919	intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20831255	GGATATCCATGCTCA[A/C/T]TTGCATTCCTTTCCC	10529
rs75328612	snp	A/C	0.0130921	0.0798413	intron-variant	NEBL	GRCh38.p7	10:20987781	GGAAGGAGATTTTCC[A/C]GGGCTCCTTCTGTAC	10529
rs75349059	snp	A/G	0.00835141	0.0640778	intron-variant	NEBL	GRCh38.p7	10:20918969	GGAAAATTCTGGAAG[A/G]AATTGACCCAAGTAA	10529
rs75354282	snp	A/G/T	0.0154538	0.0865337	intron-variant	NEBL	GRCh38.p7	10:21095754	ATCTTGATGCAATGA[A/G/T]ATGTAATATATTCCC	10529
rs75380627	snp	A/G	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20840381	CTGGGAGAGTCAGTT[A/G]GGTTATGAGTGGCAA	10529
rs75391344	snp	C/T	0.0520825	0.152737	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20858683	ACAGTATTTCAACTA[C/T]GCTTTGTGGAGATCT	10529
rs75393811	snp	A/G	0.0678174	0.1712	intron-variant	NEBL	GRCh38.p7	10:20804390	TAGTTTTCTTGATAA[A/G]TGGATCATTTGCTTT	10529
rs75398527	snp	G/T	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20972184	AACACAAAACAGTCA[G/T]GAAAGTGAAAATAAC	10529
rs75416746	snp	G/T	0.031825	0.122064	intron-variant	NEBL	GRCh38.p7	10:20896127	AAACAACCAGTATTG[G/T]GCTCATCTCTCTAAA	10529
rs75446260	snp	C/T	0.0236746	0.106192	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20849666	GTGAATCCTTGGATT[C/T]TGAACTTCCAGCCTC	10529
rs75495343	snp	C/T	0.00478085	0.0486577	intron-variant	NEBL	GRCh38.p7	10:21060696	ACCTCTCTATGCTTG[C/T]CTTCTCTAACTCCTC	10529
rs75497678	snp	A/C	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21154459	GTGAGACTCTGCTTC[A/C]AAAAAAAAAAAAAAA	10529
rs75532653	snp	C/T	0.0138799	0.0821421	intron-variant	NEBL	GRCh38.p7	10:21072222	CTTACAGACAGGTCA[C/T]TTCAATCCCTATCTT	10529
rs75534676	snp	C/T	0.0441095	0.141807	intron-variant	NEBL	GRCh38.p7	10:20804513	CTAACCAAGCACCGT[C/T]CCACTTAAGAGAGGG	10529
rs75537796	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20971591	CCCAATGCTATCCCT[C/T]CCCCCTCCCCCAACC	10529
rs75541222	snp	A/G	0.0189856	0.0955633	intron-variant	NEBL	GRCh38.p7	10:20787795	GACGGCAAACATAAC[A/G]TATGTTTAGCAACAC	10529
rs75542464	snp	A/T	0	0	intron-variant	NEBL	GRCh38.p7	10:20894541	AGAAAAAGGAAAAAA[A/T]TCTAAAAATTAAATA	10529
rs75559916	snp	A/C	0.0240643	0.107019	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20879449	TCTCCTAGCAATCTT[A/C]AACTATGTTAGAAAA	10529
rs75562535	snp	G/T	0.0799831	0.183287	intron-variant	NEBL	GRCh38.p7	10:20978519	TTCAGTGCTTTCAGA[G/T]GCCAAGGTGGAAGGA	10529
rs75564309	snp	G/T	0.0626037	0.165477	intron-variant	NEBL	GRCh38.p7	10:20996734	AGTATCATATGGACT[G/T]CCTAAAAACAGCCAG	10529
rs75565603	snp	A/G	0.171704	0.237423	intron-variant	NEBL	GRCh38.p7	10:20789254	TGAATCTATTTGTAA[A/G]GTTTGAAAGATTAAA	10529
rs75569440	snp	A/G	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:21002276	TTGTAGCAGAACTTC[A/G]TGTCCTATGCAGGAA	10529
rs75609245	snp	C/G	0.0119091	0.0762411	intron-variant	NEBL	GRCh38.p7	10:21036871	AGACACCAGGTAGGG[C/G]GAGCAACACTACTCA	10529
rs75624041	snp	C/G	0.0379877	0.132479	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20859158	TGCTGTTTTTATACT[C/G]TAATTCTAACAAGAA	10529
rs75625090	snp	C/G	0.00795532	0.062565	intron-variant	NEBL	GRCh38.p7	10:20830076	CGAACACTGAGAACA[C/G]AACACACACTTCAGG	10529
rs75626630	snp	C/G	0.0158469	0.0875917	intron-variant	NEBL	GRCh38.p7	10:21066388	AGATGATAGCAATTC[C/G]TTGTTGATAAAATGT	10529
rs75626936	snp	G/T	0.0711525	0.174681	intron-variant	NEBL	GRCh38.p7	10:21162040	GGAAGAGAGGGGGCT[G/T]GAGATTGAACAATCA	10529
rs75631381	snp	C/T	0.000798403	0.0199641	intron-variant, downstream-variant-500B	NEBL	GRCh38.p7	10:20815179	CAACTGAATTCTACG[C/T]TAACTGTATTTAAGG	10529
rs75660171	snp	C/T	0.0138799	0.0821421	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20881155	CCATTTTTATTCATC[C/T]AGCTTAAACCTCGGG	10529
rs75675804	snp	A/G	0.343254	0.231956	intron-variant	NEBL	GRCh38.p7	10:21005515	CAAGATGGGGGGATC[A/G]CTTGAGCCCAAGAGT	10529
rs75677374	snp	C/T	0.00557542	0.0525036	intron-variant	NEBL	GRCh38.p7	10:21104985	ATTAAGATAAACATA[C/T]TGTTTTTCCTTTTTA	10529
rs75683112	snp	A/T	0.0295035	0.117819	intron-variant	NEBL	GRCh38.p7	10:20900255	TGAGACCAAGAGACA[A/T]CACTTATGGCTAAAC	10529
rs75685820	snp	C/T	0.0232847	0.105357	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20865638	AGTGATGCCCATATC[C/T]CCTGTCTCTTCAACT	10529
rs75686078	snp	C/T	0.0240643	0.107019	intron-variant	NEBL	GRCh38.p7	10:20953644	TTTACTGAGGAAATG[C/T]TGCTACAATCCTTTG	10529
rs75699492	snp	A/C	0.078151	0.181571	intron-variant	NEBL	GRCh38.p7	10:21035668	GATAATGGCATAGGA[A/C]GAAAAGAAGAACTTT	10529
rs75701750	snp	A/G	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20999177	GAAAAAAAAAAAAAA[A/G]GGCTGTCAGGGAAGA	10529
rs75714135	snp	C/T	0.00557542	0.0525036	intron-variant, upstream-variant-2KB	NEBL, NEBL-AS1	GRCh38.p7	10:21172730	GAACTGTCAAGGTTC[C/T]GTCGAAACAGCACTT	10529
rs75717235	snp	C/T	0.0352966	0.128072	intron-variant	NEBL	GRCh38.p7	10:21043369	TGAAAGCCTGCAATC[C/T]TACAAAAATCCAAGA	10529
rs75722039	snp	A/G	0.0256215	0.110247	intron-variant	NEBL	GRCh38.p7	10:21006325	TTGCCAGAACAAAAC[A/G]TATTTGTGTCTTTCA	10529
rs75749825	snp	C/T	0.00398564	0.0444627	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20856323	TAAAATAAAGGTCAA[C/T]GTTCTTGAAAAGCAA	10529
rs75753510	snp	C/T	0.00795532	0.062565	intron-variant	NEBL	GRCh38.p7	10:21113673	AAATGTCATTTAGTT[C/T]GTAAAAATGGAACTC	10529
rs75761766	snp	A/G	0.00478085	0.0486577	intron-variant	NEBL	GRCh38.p7	10:20791930	ATTACTGCAACAACT[A/G]TCTAAAACAGATACC	10529
rs75769816	snp	C/T	0.0150606	0.0854603	intron-variant	NEBL	GRCh38.p7	10:20946658	GTAGAGACGAGGTTT[C/T]ACCACGCTGTTGGCC	10529
rs75779565	snp	A/G	0.030278	0.119257	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21133092	TTTTCCTCTTAGAGT[A/G]TTTTAGCTTTCACAT	10529
rs75789887	snp	A/G	0.00438332	0.0466095	intron-variant	NEBL	GRCh38.p7	10:21013969	GATCCGGAGCTGAGC[A/G]GGATACAGCAGACTG	10529
rs75800451	snp	C/T	0.0865458	0.189163	intron-variant	NEBL	GRCh38.p7	10:21015457	CCGAAAAAGGGAATG[C/T]TTTCTACCACATGAT	10529
rs75803264	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20926479	AACCATGTGCCTGAT[A/G]CTCTGCCTATACCTA	10529
rs75810557	snp	C/T	0.0865458	0.189163	intron-variant	NEBL	GRCh38.p7	10:20902082	AGCAACCTAAACATG[C/T]GTCACCATGACCAAG	10529
rs75810674	snp	C/G	0.021333	0.101051	intron-variant	NEBL	GRCh38.p7	10:21050605	AAGAAAGTGAGGAAC[C/G]GGTGCAGCGTGGGCG	10529
rs75813485	snp	A/G	0.0744748	0.178019	intron-variant	NEBL	GRCh38.p7	10:21040503	CGAAGGAGAAATAGA[A/G]GAGAGAAGGAGATGC	10529
rs75820862	snp	A/G	0.0252325	0.109451	intron-variant	NEBL	GRCh38.p7	10:21039621	CAGTAACCACTGAAC[A/G]TAACTTAAAATGGTG	10529
rs75821346	snp	C/T	0.00755907	0.0610114	intron-variant	NEBL	GRCh38.p7	10:20825043	TTAAGCCTAGGTCCT[C/T]CTTACACTTTATTCA	10529
rs75824647	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21019443	GCAATGTAGTTGCTC[C/T]GTGTCTTACTATGGG	10529
rs75829958	snp	C/G	0.0517044	0.152246	upstream-variant-2KB, intron-variant	C10orf113, NEBL	GRCh38.p7	10:21148275	TACATTGGTTTCCAT[C/G]CACGTTCATGGCTCA	10529
rs75839660	snp	A/T	0.0205511	0.0992634	intron-variant	NEBL	GRCh38.p7	10:20933426	GAGTGGCAGGTAAAT[A/T]TAAACCTTAAAAAGT	10529
rs75844366	snp	A/G	0.0854556	0.188216	intron-variant	NEBL	GRCh38.p7	10:20822237	CAGGGCATACCTCTC[A/G]TCTTTAAAATCCCCC	10529
rs75880934	snp	A/G	0	0	intron-variant	NEBL	GRCh38.p7	10:21095337	AAGAAAAGCAGATAA[A/G]AGATAAGACGAACAT	10529
rs75885498	snp	G/T	0.5	0	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20854071	AAAATAATTATTTCA[G/T]GATTTCTATCATTGG	10529
rs75903914	snp	A/G/T	0.00911567	0.0668952	NEBL, LOC102725112	10	allele_origin=G(germline)/A(germline)	10:20852527	GGGAGGGTAGGTACC[A/G/T]TACGGGCAAGTGTGT	10529
rs75907214	snp	C/T	0.0524604	0.153226	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21145782	CAAGGCTAACCTGCA[C/T]GCAAACCCTGTAGGG	10529
rs75912838	snp	A/C	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20823985	GCTTCTACTTCACTC[A/C]AAATCTCCCCCATCA	10529
rs75921255	snp	C/T	0.00716266	0.059414	intron-variant	NEBL	GRCh38.p7	10:20804342	TAGCCCAAACAATTC[C/T]ATACAAAGTTCCCCT	10529
rs75932093	snp	C/T	0.0182019	0.0936463	intron-variant	NEBL	GRCh38.p7	10:21093308	CCCAGAAGCATTGGA[C/T]GCATTTTATCATAGG	10529
rs75938474	snp	A/G	0.0869089	0.189476	intron-variant	NEBL	GRCh38.p7	10:20822995	GTATGTCTGAATAAT[A/G]TGTGTCTTTAATAAA	10529
rs75945401	snp	C/T	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:20839320	GGATTGGACATGTCA[C/T]GGCAACAGAAGAATT	10529
rs75947047	in-del	-/A	0.0221141	0.102801	intron-variant	NEBL	GRCh38.p7	10:20830718	AAAAGCATTTGAGCC[-/A]AGTGTCCAATAGGGT	10529
rs75968091	snp	A/G	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:20791083	TTAAAGCCACAAATA[A/G]TAGTTTTAGTTATAC	10529
rs75998910	snp	A/G	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20808362	TTTAAAAAAAAAAAA[A/G]GACTATTAACTTTCT	10529
rs76005264	snp	A/G	0.0115144	0.0749975	intron-variant	NEBL	GRCh38.p7	10:21068424	GCTACAGGGATGGCC[A/G]TGTGACTAGAATCAG	10529
rs76011673	in-del	-/A	0.186105	0.241697	intron-variant	NEBL	GRCh38.p7	10:21152727	CACTCTGAATTTAAG[-/A]ACCTCAGAACAGTAA	10529
rs76016750	snp	A/C/G	0.0236746	0.106192	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20850118	AATTAACATTTGAAA[A/C/G]TGTCAGTTATATTAT	10529
rs76032558	snp	C/T	0.0482946	0.147699	intron-variant	NEBL	GRCh38.p7	10:20828745	GAGAGTAAAAAACTG[C/T]TTTTACTGACTTACA	10529
rs76040518	snp	A/G	0.0839998	0.186933	intron-variant	NEBL	GRCh38.p7	10:21011559	GGGACCCATGCCCAC[A/G]TTCCCTCCTTCTCTC	10529
rs76047773	snp	A/C	0.0460142	0.144533	intron-variant	NEBL	GRCh38.p7	10:21084597	GCAAGACTCTGTCCC[A/C]AAAAAAAAATAAAAA	10529
rs76071321	snp	C/G	0.0402882	0.136092	intron-variant	NEBL	GRCh38.p7	10:21005325	GCAGGGAGACCCCCA[C/G]CTGGTCAAATTGGCC	10529
rs76074823	snp	A/G	0.0221141	0.102801	intron-variant	NEBL	GRCh38.p7	10:20832407	TATTCAATCATAAGA[A/G]CAACAAATAAGTTAT	10529
rs76077902	snp	A/G	0.0189856	0.0955633	downstream-variant-500B	NEBL	GRCh38.p7	10:20779913	CAGTGTGCTTGATTC[A/G]TAATACTATTAAAAT	10529
rs76082434	snp	C/T	0.00279162	0.0372561	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20869279	TGGTATTAACTAAAG[C/T]GGGCACCTTAGAGAA	10529
rs76091611	snp	A/T	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21004292	ATCATTAATAAAAAA[A/T]TAAAAATTCAAAGCC	10529
rs76098498	snp	G/T	0.0748431	0.178382	intron-variant	NEBL	GRCh38.p7	10:20810340	ATAGGAAACAATTGA[G/T]AAGTTTATGTTTAAA	10529
rs76116418	snp	A/C	0.030665	0.119967	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21139990	ACCCTGTCTCAACAA[A/C]AAAAAAAAAAAAAAA	10529
rs76126182	snp	A/T	0.0722614	0.17581	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20855308	ACTTTATAATTTGAT[A/T]AGAAGTTATCTTGTA	10529
rs76167663	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21064896	GGAAATTAGGTGGTT[C/T]GGACAAGCAGGAAAA	10529
rs76168516	snp	A/G	0.0271762	0.113356	intron-variant	NEBL	GRCh38.p7	10:21017665	TGGAATGCACTGAAG[A/G]CATCTATAACCACTA	10529
rs76168538	snp	C/T	0.0524604	0.153226	intron-variant	NEBL	GRCh38.p7	10:21070089	GAAAGAATAATACTG[C/T]ATCCACTAGTAGCTG	10529
rs76172221	snp	C/T	0.0221141	0.102801	intron-variant	NEBL	GRCh38.p7	10:20956123	AAGTTCTGCTCTACA[C/T]GGAAAAATAAAGCAA	10529
rs76177254	snp	G/T	0.0236746	0.106192	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20848184	CTGCTGCAGAAAAAA[G/T]TGCTGCTGCAGTGGA	10529
rs76183781	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21040338	AGTAAGACTCCATTC[A/C]AAAAAAAAAGAAAGA	10529
rs76214694	snp	A/C	0.0146672	0.084371	intron-variant	NEBL	GRCh38.p7	10:20937049	GTGTGATCTGGAAGG[A/C]TTTAAAATTGCACCT	10529
rs76222543	snp	A/G	0.0134861	0.0810011	intron-variant	NEBL	GRCh38.p7	10:21045243	GAATCAAAAGAAAAT[A/G]TATGCTCAGAGATGA	10529
rs76227060	snp	C/T	0.0236746	0.106192	intron-variant	NEBL	GRCh38.p7	10:20931491	AATGTTCCTCTAAAC[C/T]AACAAAGATATGGGA	10529
rs76227705	snp	G/T	0.0236746	0.106192	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20851895	TTAAAACCAATGAAG[G/T]TGAGTACGAAATTAT	10529
rs76231356	snp	A/G	0	0	intron-variant	NEBL	GRCh38.p7	10:20976937	TAAAAAAAAAAAAAA[A/G]AAGTGCTTCAGGTCC	10529
rs76243466	snp	C/T	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:20894128	CCAAAGAGTAACAAT[C/T]AGGCTGCACCATGAA	10529
rs76252762	snp	A/G	0.0103295	0.0711199	intron-variant	NEBL	GRCh38.p7	10:20980475	AATAAACAGGCAGAT[A/G]TACAAACACCTGCAG	10529
rs76260072	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21015035	TGCCCTCATAAATTA[A/C]ACATACTCCATTTAA	10529
rs76261504	snp	A/G	0.226484	0.248892	intron-variant	NEBL	GRCh38.p7	10:20808192	TTCTCCTATGACTGT[A/G]TAGTGTGTATATTTA	10529
rs76262755	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20936763	CTGCCTGTTCTAATT[A/G]TTGCCTTTTCTGACC	10529
rs76264397	snp	C/T	0.0185938	0.0946107	intron-variant	NEBL	GRCh38.p7	10:20824610	TTAAAAGGGCAACTT[C/T]CCATTTGAATACTAA	10529
rs76277321	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21045232	GTAAATTAATAGAAT[C/T]AAAAGAAAATGTATG	10529
rs76296059	snp	C/T	0.00478085	0.0486577	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20883064	ACCTTACATGCTCTC[C/T]TCAGCCCAAATCCGA	10529
rs76301843	snp	A/T	0.0471551	0.14613	intron-variant	NEBL	GRCh38.p7	10:21012528	CCATGCCTAGCTTAT[A/T]TATTTTTATTTGTTA	10529
rs76309993	snp	A/C	0.0134861	0.0810011	intron-variant	NEBL	GRCh38.p7	10:21056437	AGACTGACTGTCCTC[A/C]CGGAACTTTAAAAGC	10529
rs76315559	snp	A/G	0.0729998	0.176553	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21144081	TTCTCTGGTCTCTGT[A/G]ATGAGAGGCATCTGC	10529
rs76333139	snp	A/G	0.0111196	0.0737302	intron-variant	NEBL	GRCh38.p7	10:21043991	CCTTTCTACAGATTC[A/G]TCTAAAAACAGGGTA	10529
rs76334890	snp	C/T	0.0232847	0.105357	intron-variant	NEBL	GRCh38.p7	10:20892401	CCACCATACTAATGA[C/T]GACAGAATAGAAGGA	10529
rs76376228	snp	C/T	0.148996	0.228688	intron-variant	NEBL	GRCh38.p7	10:20990401	TGAGGACAGGGACCT[C/T]GTGATTGGGATTAGT	10529
rs76390638	snp	A/G	0.0729998	0.176553	intron-variant, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20879635	GGTCAGCCAAGCACC[A/G]TTCCATAAAGGGACT	10529
rs76392216	snp	A/C	0.0240643	0.107019	intron-variant, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20879689	GAGATGGCAACTGTA[A/C]TTCAGGTACTTTTCC	10529
rs76400717	snp	A/T	0.0217236	0.101931	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20861814	GCATATGCTCTCCCA[A/T]GTAAATGTTACAGAC	10529
rs76424622	snp	A/G	0.0134861	0.0810011	intron-variant	NEBL	GRCh38.p7	10:21045035	AGAACGTTAATTATA[A/G]ACTATTTTGCTAAAA	10529
rs76444897	snp	C/T	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20912881	CATAGTATGCCAATT[C/T]TTTTTTTTTTTTTTT	10529
rs76464362	snp	A/G	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20954026	AAACTCTTCTTAAGG[A/G]AAAAAAAAAAAAAAA	10529
rs76465430	snp	A/C	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21024081	GGGAAAAAAAAAAAA[A/C]ACATTGAAAAGCTTC	10529
rs76473813	snp	A/G	0.5	0	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21128139	TTATAACCAAATTCA[A/G]AGGAAACACAAACAG	10529
rs76494147	snp	C/G	0.0471551	0.14613	intron-variant	NEBL	GRCh38.p7	10:20995179	TCTTGAAAAGAAATG[C/G]TTATTCCCCTCTGAG	10529
rs76496987	snp	C/G	0.02016	0.0983543	intron-variant	NEBL	GRCh38.p7	10:20948938	TCTCTTTTCCTTTCA[C/G]TAGCTCTGTCCTCAA	10529
rs76508636	snp	A/C			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20845919	GAGAATATTTCTCTA[A/C]CATCTATGGTGTTTG	10529
rs76545977	snp	C/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21101448	TTCTGCTACCCCTTC[C/T]TGTTAGAGGGAAAGT	10529
rs76546614	snp	C/T	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20793574	TTTTTTTTTTTTTAA[C/T]ACAGGATCTGGCTCT	10529
rs76552001	snp	A/C	0.0232847	0.105357	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20855828	GATGTTGCTAAAGAC[A/C]TCTAGGGGTCTTTAA	10529
rs76558365	snp	C/T	0.0256215	0.110247	intron-variant	NEBL	GRCh38.p7	10:21006243	CGGTGCTGTCATAGA[C/T]ATCCTTGTACTTACG	10529
rs76575400	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21169118	TATATTTGGACATAT[A/T]ATTAGATCAAAATAT	10529
rs76575526	snp	C/G	0.0182019	0.0936463	intron-variant	NEBL	GRCh38.p7	10:21163038	TAATCCTAAGAGATA[C/G]AGTCTATTATACCCA	10529
rs76577880	snp	C/T	0.00597247	0.0543191	intron-variant	NEBL	GRCh38.p7	10:21099515	CCCAACCACCACCCC[C/T]TTCAATTTCCTCTCT	10529
rs76585556	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21112961	AACTGGAAAGTGATC[C/T]GCCCCTGGAAGTGGT	10529
rs76590732	snp	A/C	0.0142736	0.0832652	intron-variant	NEBL	GRCh38.p7	10:20836779	TTTTCTTCCTTTACA[A/C]CCAATAAAACTCTGC	10529
rs76605508	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20802236	CACATTGCAGGCAAT[A/G]AACTAGAGGCAAACA	10529
rs76634629	snp	A/G	0.0123036	0.0774623	intron-variant	NEBL	GRCh38.p7	10:20969367	TAAGCTTTCAATTAA[A/G]CTTCCACTGCATTCC	10529
rs76638898	snp	A/G	0.0158469	0.0875917	intron-variant	NEBL	GRCh38.p7	10:20810655	ATTTTAATAACTTCT[A/G]AATTCACCAGTCTCT	10529
rs76654330	snp	C/G	0.0189856	0.0955633	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20781686	ATGGGTTCAAGTAGT[C/G]TAAGCATCACAGAAT	10529
rs76662732	snp	A/T	0.0263992	0.111815	intron-variant	NEBL	GRCh38.p7	10:21005756	AATAATAAATTAAAT[A/T]AAATCACTATTTTAT	10529
rs76665596	snp	A/C	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:21152109	GTGCATTTCCGCTAT[A/C]CGGAAATGGGACAGA	10529
rs76692699	snp	G/T	0.0248432	0.108648	intron-variant	NEBL	GRCh38.p7	10:20928366	TGCTACACAGCTGAG[G/T]GCTAAGGTAAAAAAA	10529
rs76712169	snp	C/T	0.0596104	0.162024	intron-variant	NEBL	GRCh38.p7	10:21090540	ACCTACCCCCACAGA[C/T]ATTGAGGGACTGTAT	10529
rs76712171	snp	C/T	0.0158469	0.0875917	intron-variant	NEBL	GRCh38.p7	10:21086274	TTATCCAAAACTGCA[C/T]GATTTGTGTAAGGAG	10529
rs76718496	snp	A/C/T	0.0183498	0.0940143	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21126185	CATAGAAAGGAAAAA[A/C/T]AATACCACATTTGGA	10529
rs76725479	snp	A/T	0.0364509	0.129988	intron-variant	NEBL	GRCh38.p7	10:20954478	GCAGCTAGGGAAAGA[A/T]GGTGTTGCAGGACTT	10529
rs76751597	snp	C/G	0.00597247	0.0543191	intron-variant	NEBL	GRCh38.p7	10:20999703	TTTTCCCTACACTCA[C/G]TGGGACCTATCTAAG	10529
rs76767397	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21169116	TATATATTTGGACAT[A/T]TAATTAGATCAAAAT	10529
rs76774966	snp	C/T	0.0283406	0.115616	intron-variant	NEBL	GRCh38.p7	10:21167607	AATTTTAAGAACCGA[C/T]GTATATTTTAAAAAG	10529
rs76775554	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21041423	AGCAAAGACAACATC[A/C]TCATCACCACTAACA	10529
rs76786441	snp	A/C	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21166219	AGCGAGACTGTGTCT[A/C]AAAAAAAAAAAAAAA	10529
rs76824049	snp	A/G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20976938	AAAAAAAAAAAAAAA[A/G/T]AGTGCTTCAGGTCCT	10529
rs76833805	snp	A/G	0.0352966	0.128072	intron-variant	NEBL	GRCh38.p7	10:21085382	ATCCCAGAAGTTTGG[A/G]AAGCCGAGGCGGAAG	10529
rs76839105	snp	A/G	0.0267878	0.112589	intron-variant	NEBL	GRCh38.p7	10:21082635	TCCTCACCTAATTCC[A/G]ATGCCCATTTTGATC	10529
rs76843659	snp	A/C	0.00438332	0.0466095	intron-variant	NEBL	GRCh38.p7	10:20842250	ATCTGAGTCAAATGA[A/C]CCGAGTGAAAGTCAG	10529
rs76849059	snp	C/T	0.030665	0.119967	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21127064	CTGATTCAATACACT[C/T]AAACGCATCCATGGT	10529
rs76850921	snp	A/G	0.00716266	0.059414	intron-variant	NEBL	GRCh38.p7	10:20805911	AGTCACTGAGTCATC[A/G]CTGCTGTCCAAAATC	10529
rs76852065	snp	C/G	0.0341408	0.126114	intron-variant	NEBL	GRCh38.p7	10:20823374	GAGAATTCTTCAATT[C/G]TAACTATTGCATAAT	10529
rs76857674	snp	C/T	0.00835141	0.0640778	intron-variant	NEBL	GRCh38.p7	10:21090985	AGCGTCCCACCACCA[C/T]CCACCCAGCCACCCC	10529
rs76859638	snp	C/T	0.0854556	0.188216	intron-variant	NEBL	GRCh38.p7	10:21163307	TGTGGTGGCAGGAAA[C/T]GCATGAAGCTCAGGA	10529
rs76874340	snp	C/T	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20821982	ACTCCAACGTTACCC[C/T]TTCCCCAAGGCTCTT	10529
rs76877420	snp	G/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21159183	TCAATCAGGATTTTA[G/T]TTTTCAAAGTCTTCT	10529
rs76886011	snp	A/G	0.030665	0.119967	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20784521	AAAATGGAAAAGGAC[A/G]TCTTTTGATTAACCC	10529
rs76923986	snp	C/T	0.0123036	0.0774623	intron-variant	NEBL	GRCh38.p7	10:20807719	GTTGAAAGGGAAATT[C/T]AGTATTGCTTTTGTT	10529
rs76954003	snp	C/T	0.0410537	0.137264	intron-variant, downstream-variant-500B	NEBL	GRCh38.p7	10:20815438	GGAAATAACAAAGAG[C/T]TGCAAAATAATGTAA	10529
rs76958219	snp	C/T	0.111606	0.2082	intron-variant	NEBL	GRCh38.p7	10:20838753	TCAGCAGCCACCATC[C/T]TGATCAGTCGGCAGC	10529
rs76960798	snp	A/G	0.0271762	0.113356	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20846236	ATATCTACTAAACAA[A/G]GGCCCAGATTTTACC	10529
rs76967061	snp	C/T	0.0158469	0.0875917	intron-variant	NEBL	GRCh38.p7	10:21078037	ACTCTCAATACCAGA[C/T]TATTCTGAAAGCTGG	10529
rs76972125	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21046905	CCGCGCCCGGCCCCT[A/C]ACCTCAATATTTTTA	10529
rs76983495	snp	A/T	0.046775	0.145601	intron-variant	NEBL	GRCh38.p7	10:21089666	GGAGGCTGCTCTCAA[A/T]GATTGATAGGTGAAT	10529
rs77002191	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21098046	GTGCTGATAACAACA[A/G]TTATCTAAATGTTGC	10529
rs77009558	snp	A/C	0.0174175	0.0916809	intron-variant	NEBL	GRCh38.p7	10:20829134	ACTGAAGTACTAGAT[A/C]GTAAGTATCAGAGCC	10529
rs77023742	snp	C/G	0.129664	0.219133	intron-variant	NEBL	GRCh38.p7	10:20816363	GTCGTGGTTTCTTAG[C/G]AATTAACTGCGGCAG	10529
rs77059895	snp	C/T	0.0271762	0.113356	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20873312	CATGACAATGTGGTG[C/T]TCTATAAATCTTGTT	10529
rs77078981	snp	A/G	0.0509478	0.151255	intron-variant	NEBL	GRCh38.p7	10:21049473	AGAACCAAACTCAAC[A/G]GGGATGAGACACCAC	10529
rs77079781	snp	A/T	0.0225045	0.103662	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21127918	ACCAATAAAATGTGA[A/T]CATGAACTGTGTTAA	10529
rs77088207	snp	A/T	0.0103295	0.0711199	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20872370	TGTCAGATCTTCCAG[A/T]ATATCACTCCTTGGG	10529
rs77100476	snp	A/C	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20980344	CAGAACAAAAAGAAC[A/C]AAAAAAAAAGTTTCT	10529
rs77105855	snp	A/G/T	0.0166325	0.0896639	intron-variant	NEBL	GRCh38.p7	10:21110999	CCATTCACAATTGCT[A/G/T]CAAAGAGAATAAAAC	10529
rs77136151	snp	A/T	0.00923755	0.0673308	intron-variant	NEBL	GRCh38.p7	10:20889998	AAAGAAAAACAATTC[A/T]AATGGCCTTTTTTGA	10529
rs77141181	snp	C/T	0.0352966	0.128072	intron-variant	NEBL	GRCh38.p7	10:21041029	AGTCTCAGGTAGTTC[C/T]TTATAGCAATGTAAA	10529
rs77148485	snp	A/T	3.3066e-05	0.00406595	intron-variant	NEBL	GRCh38.p7	10:20817724	AGAACTTTAACAGAT[A/T]GCACAATGGGCTCCA	10529
rs77168119	snp	C/G/T	0.0240737	0.107104	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21136862	ACATAACTTCTTACT[C/G/T]GTCTCTGGATGGAGG	10529
rs77170454	snp	A/G	0.0126979	0.078662	intron-variant	NEBL	GRCh38.p7	10:20894976	ATAATCATGTCCTAA[A/G]TTTAAGTAGTACATT	10529
rs77179112	snp	A/G	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21064908	GTTTGGACAAGCAGG[A/G]AAAAAAAAATATTTA	10529
rs77201584	snp	A/G	0.0479149	0.147179	intron-variant	NEBL	GRCh38.p7	10:21097966	AATTTGTGACCCTAC[A/G]TGAAATGAACATTCG	10529
rs77207008	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20996400	CGAAGTGAAAATGCA[A/G]AGTATCCTGAAGACA	10529
rs77207874	snp	A/G	0.0337553	0.125452	intron-variant	NEBL	GRCh38.p7	10:21102593	GAGTGCAGTTGTCTT[A/G]CTGGCATGCTTGACA	10529
rs77224094	snp	A/C	0.0252325	0.109451	intron-variant	NEBL	GRCh38.p7	10:20924388	ATGTGTATCAAATGC[A/C]TATAGCTCTCGATCA	10529
rs77236112	snp	C/G	0.0737376	0.17729	intron-variant	NEBL	GRCh38.p7	10:20832799	TTTGCCTCCTATCTT[C/G]CACTCATAATCCTTC	10529
rs77245635	snp	C/G	0.0547245	0.156101	intron-variant	NEBL	GRCh38.p7	10:21156307	TTTTGTACAAATGGA[C/G]AAAGAGTTATCAAAA	10529
rs77251977	snp	A/C/T	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:21042677	GAGTATTTTTCACCA[A/C/T]AGAAAATCGCAAACA	10529
rs77261719	snp	A/T	0.0444908	0.142359	intron-variant	NEBL	GRCh38.p7	10:20805114	ACTAGACATGGGGTA[A/T]GAGTGAAAGACAAGC	10529
rs77263204	snp	A/T	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20912879	GCCATAGTATGCCAA[A/T]TCTTTTTTTTTTTTT	10529
rs77270987	snp	C/T	0.0486741	0.148216	intron-variant	NEBL	GRCh38.p7	10:21087442	GATATGTACAGAATG[C/T]CACCTAGAATCCCAA	10529
rs77275970	snp	C/T	0.0448719	0.142907	intron-variant	NEBL	GRCh38.p7	10:21022827	CACACAGCATTCGGT[C/T]CTGCCTCATCTTCTC	10529
rs77283698	snp	C/T	0.00953873	0.0683987	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20877964	TTCCTTGTGTGTGTC[C/T]GTGTCCTTAATTTTC	10529
rs77288884	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:20795125	TGAATTCAGAAAAGT[G/T]TAAGAGTACTATGGC	10529
rs77295246	snp	C/T	0.00676609	0.0577691	intron-variant	NEBL	GRCh38.p7	10:21065951	ACCAGCAGCTGCACA[C/T]CTCTCTTCAACCTGG	10529
rs77299961	snp	A/C	0.483995	0.0880135	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20855525	GAAAACAAAACAAAA[A/C]AAAAAAAAAACGAAG	10529
rs77314108	snp	G/T	0.0448719	0.142907	intron-variant	NEBL	GRCh38.p7	10:20994398	CCAAAAAGAGTAATT[G/T]CGTCTATAATATACA	10529
rs77319174	snp	C/T	0.0263992	0.111815	intron-variant	NEBL	GRCh38.p7	10:21165601	TGCCAGGCTCATCTA[C/T]GGCCATACCACCCTG	10529
rs77320324	snp	A/G	0.0244538	0.107838	intron-variant	NEBL	GRCh38.p7	10:21081290	CACCATTTGAGTTGT[A/G]GGGAGCTCCAGCAGC	10529
rs77321185	snp	A/G	0.00279162	0.0372561	upstream-variant-2KB, intron-variant	C10orf113, NEBL	GRCh38.p7	10:21146905	AGCTCTGGGAGATAG[A/G]CCTTAGGGTTTTAGT	10529
rs77322342	snp	A/G	0.0460142	0.144533	intron-variant	NEBL	GRCh38.p7	10:20903705	AAAGAACAAAATAAC[A/G]TATTTTGTAGCAACT	10529
rs77325185	snp	C/T	0.0573587	0.15934	intron-variant	NEBL	GRCh38.p7	10:21085807	AAATGTAGGACCTCA[C/T]GGCAACAGGACAAAA	10529
rs77352066	snp	A/C	0.0174175	0.0916809	intron-variant	NEBL	GRCh38.p7	10:20814321	GTAAACCTGCGCAAG[A/C]CCGAGGACTCGTATC	10529
rs77369206	snp	A/C	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20985522	ACCAGAACATGGATC[A/C]AAAAAACTCATTACC	10529
rs77370480	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:20818453	AGTAGCGCTGCCTTG[G/T]TAACTATTTTTGCTT	10529
rs77381907	snp	A/C	0.021333	0.101051	intron-variant	NEBL	GRCh38.p7	10:20821450	TATCCAAATTTCCCA[A/C]ATTTCTGCCATTTGC	10529
rs77385250	snp	A/T	0.5	0	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20959789	AAAAAGTTTTTTTTT[A/T]AAAAAAAGATGTTGT	10529
rs77390379	snp	C/T	0.081446	0.184634	intron-variant	NEBL	GRCh38.p7	10:20979710	TTTTTAATTCATTTA[C/T]GTGTTTGTTTAGTAG	10529
rs77393904	snp	C/T	0.0138799	0.0821421	intron-variant	NEBL	GRCh38.p7	10:20931952	GCATATTCTTTCATG[C/T]ATTCCTTCCCTGGTC	10529
rs77396928	snp	A/T	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21121122	CCCTGAAACTTTTTT[A/T]AACAGTATCTACCAA	10529
rs77408923	snp	A/G	0.0471551	0.14613	intron-variant	NEBL	GRCh38.p7	10:21120346	CACAACTGCACTCAA[A/G]CCTGGGCAACAGAGT	10529
rs77424929	snp	A/C	0.00597247	0.0543191	intron-variant	NEBL	GRCh38.p7	10:20964622	TCCCATTAGTGCATA[A/C]CTTCAATGCTCAGGA	10529
rs77428179	snp	A/G	0.143959	0.226396	intron-variant	NEBL	GRCh38.p7	10:20968090	GCAGAAAGTTAAATC[A/G]GCCACTCTGAGTTTC	10529
rs77428407	snp	C/T	0.0162398	0.0886349	intron-variant	NEBL	GRCh38.p7	10:21089609	TGGTGTACTGGTACC[C/T]GGCAAAAAGTGGGTG	10529
rs77434336	snp	A/C	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20902408	AAAGACACTGTCTCA[A/C]AAAAAAAAAAATTTA	10529
rs77445663	snp	G/T	8.31373e-05	0.00644684	intron-variant	NEBL	GRCh38.p7	10:20831184	TTCTGAGCATCTTCA[G/T]TCATGACCAACCTGG	10529
rs77456781	snp	A/G	0.0402882	0.136092	intron-variant	NEBL	GRCh38.p7	10:21006166	GCAGATTATCAAAAT[A/G]TAACTCACTATTCTC	10529
rs77463307	snp	A/G	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20989249	ATTTCCCCCCAACTT[A/G]CCTAGTTTAAAAACA	10529
rs77463910	snp	A/G	0.00993419	0.0697739	intron-variant	NEBL	GRCh38.p7	10:20974025	AGTTAATGAGCATTG[A/G]GTACTTTTATCACTT	10529
rs77464128	snp	A/T	0.0460142	0.144533	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20898587	GGGAAAAAAGCAGGT[A/T]TCTTAAACAAATATG	10529
rs77485933	snp	C/G	0.0551013	0.156571	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21141307	ATGGTATTTATGTAA[C/G]GGAATGCCTTCGTTT	10529
rs77492055	snp	A/G	0.0170251	0.090679	intron-variant	NEBL	GRCh38.p7	10:20930105	AGTTTCACACTAGTA[A/G]AGAGAACAGCTTAAC	10529
rs77500119	snp	A/G	0.00874735	0.0655527	intron-variant	NEBL	GRCh38.p7	10:21104886	GCCCGATATCAGGAT[A/G]AAGAAGTTTCCATCT	10529
rs77520476	snp	G/T	0.0146672	0.084371	intron-variant	NEBL	GRCh38.p7	10:21030457	TCCAACTTCTAAATC[G/T]ACCAAAACTGATCAG	10529
rs77534163	snp	C/T	0.0433465	0.140692	intron-variant	NEBL	GRCh38.p7	10:21017116	CCAAGACCTATTCCG[C/T]ACCAGCTAAGTGTGA	10529
rs77546965	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21169117	ATATATTTGGACATA[G/T]AATTAGATCAAAATA	10529
rs77559905	snp	C/G	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:21027706	TAGCTCCTCCTCTCT[C/G]AGTTAGGAGAGAGAC	10529
rs77562352	snp	A/T	0.0138799	0.0821421	intron-variant	NEBL	GRCh38.p7	10:21045784	TAAATTAGTATAGCC[A/T]TTATGGAAAACAGCA	10529
rs77565979	snp	A/T	0	0	intron-variant	NEBL	GRCh38.p7	10:20830916	TCTCTAAAATTTAAA[A/T]AAAAAAAAAAAAAAA	10529
rs77568544	snp	A/C	0.0460142	0.144533	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21140598	TTGTTCTTATTTCCT[A/C]CTCTACTTTCTAGAT	10529
rs77568868	snp	A/C	0.0678174	0.1712	intron-variant	NEBL	GRCh38.p7	10:21007891	ACAGTTTTTCACATT[A/C]GCTATTTCTTAAAAC	10529
rs77577043	snp	G/T	0.0165278	0.0893908	intron-variant	NEBL	GRCh38.p7	10:20902654	CTACATTAACATAGC[G/T]CCCATTGAGCTGAAA	10529
rs77614538	snp	C/T	0.0341408	0.126114	intron-variant	NEBL	GRCh38.p7	10:21051496	TACCCCCAAAGAAAA[C/T]ATCTACATAATATAC	10529
rs77627056	snp	A/G	0.0333695	0.124785	intron-variant	NEBL	GRCh38.p7	10:21009950	TACCGCAGGCTGCTG[A/G]TTACCCCTAGAGTTA	10529
rs77639453	snp	C/T	0.0111196	0.0737302	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20851405	ACCTATTTGTAGACA[C/T]AATTTTGTTGCAAAG	10529
rs77643565	snp	A/C	0.0248432	0.108648	intron-variant	NEBL	GRCh38.p7	10:20818641	TTCTCCATTAACTGC[A/C]TTTTTTTAAAGAGAT	10529
rs77676481	snp	G/T	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20912900	TTTTTTTTTTTTTTT[G/T]TAGACAGAGTCTCTC	10529
rs77679113	snp	C/T	0.0383715	0.133092	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20862366	ACCACAATAGTAACA[C/T]AACTACATTATATAA	10529
rs77685592	snp	A/G	0.0429648	0.14013	intron-variant	NEBL	GRCh38.p7	10:21054103	GGCAAAATGGACAAA[A/G]TAGGAGAAAAATTGA	10529
rs77686523	snp	A/G	0.00953873	0.0683987	intron-variant	NEBL	GRCh38.p7	10:21046898	TGAGCCACCGCGCCC[A/G]GCCCCTAACCTCAAT	10529
rs77696664	snp	C/T	0.0444908	0.142359	intron-variant	NEBL	GRCh38.p7	10:20805263	ACTTATAAGGTTTGA[C/T]ATATGTCACTAATCA	10529
rs77698507	snp	C/T	0.135143	0.222054	intron-variant	NEBL	GRCh38.p7	10:20804402	TAAGTGGATCATTTG[C/T]TTTATCAACCCTCAT	10529
rs77752304	snp	A/G	0.0283406	0.115616	intron-variant	NEBL	GRCh38.p7	10:20912211	TGTTTTATAGTTTCC[A/G]TTGTATTACCATGTC	10529
rs77778702	snp	C/T	0.0341408	0.126114	intron-variant	NEBL	GRCh38.p7	10:20805352	ATTAGCATATTCCAA[C/T]GTATCCTAAAATCTT	10529
rs77779178	in-del	-/A	0.272511	0.248984	intron-variant	NEBL	GRCh38.p7	10:20995932	TTACAGTTTATTATG[-/A]AAAAAAAAATCTGCA	10529
rs77787818	snp	A/G	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20994884	AGGAGGAGGAGGTAG[A/G]GGGGGGGGTTGGTCT	10529
rs77799099	snp	A/T	0.5	0	upstream-variant-2KB	NEBL	GRCh38.p7	10:21175508	TGTCATTTCAAAAAA[A/T]TATCATGGCTGCAGC	10529
rs77803502	snp	G/T	0.00557542	0.0525036	intron-variant	NEBL	GRCh38.p7	10:21054920	ATAAACACAAAGACA[G/T]ATTTCAATGCTTTAG	10529
rs77818446	snp	A/T	0.0217236	0.101931	intron-variant	NEBL	GRCh38.p7	10:21005504	GTTTGCAAGGTCAAG[A/T]TGGGGGGATCGCTTG	10529
rs77844991	snp	C/T	0.0142736	0.0832652	intron-variant	NEBL	GRCh38.p7	10:21065619	TCTTAATGCAAAACC[C/T]GTCACATCCACCTCT	10529
rs77845879	snp	A/G	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:20918578	ATTGGGGCCGGGCAC[A/G]GCTGGCTCATGCCTG	10529
rs77854178	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20958211	GTATTCCTCAATTCA[C/T]ATTTGGACACTGTCC	10529
rs77889422	snp	A/G	0.0588605	0.161139	intron-variant	NEBL	GRCh38.p7	10:20962913	TGTTTCTGTTGAATC[A/G]TGTCTGTATTTAAAT	10529
rs77904949	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21009138	TGGTTTTAATTTTAA[C/T]GGTTTATAAGCATTA	10529
rs77911366	snp	C/T	0.0433465	0.140692	intron-variant	NEBL	GRCh38.p7	10:21005089	TCCATTTTGCACGCT[C/T]ACAACCAAATAAACA	10529
rs77932198	snp	C/G	0.0232847	0.105357	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20780035	ATCAATTTACAATTA[C/G]GAAGGATTATGAGCC	10529
rs77962718	snp	A/G	0.0166325	0.0896639	intron-variant	NEBL	GRCh38.p7	10:21041124	GGTAGACTGTATGTC[A/G]TGGGGGTTTGGTGTA	10529
rs77963533	snp	A/G	0.00318978	0.0398085	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21133747	CTCAAAATAATAGCC[A/G]TGTAGGGTTTGGTTG	10529
rs77967318	snp	G/T	0.0240643	0.107019	intron-variant	NEBL	GRCh38.p7	10:20885981	GTAATAGTGAAACAC[G/T]TAAAGGTGTTCTGCA	10529
rs77974098	snp	C/T	0.0479149	0.147179	intron-variant	NEBL	GRCh38.p7	10:21098132	GATATGAATTTATAA[C/T]AGCAATAGGGCTAAA	10529
rs77975629	snp	C/G	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20964479	GGAGCCAGCGTGTCA[C/G]ATGGCAAGACAGGGA	10529
rs77980334	snp	A/G	0.00199481	0.0315187	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21134775	CAAATCACGTCTTGG[A/G]TGATTACTGAGTTCT	10529
rs77984789	snp	A/G	0.0707826	0.174302	intron-variant	NEBL	GRCh38.p7	10:21006153	CATATTCTTTGGTGC[A/G]GATTATCAAAATGTA	10529
rs78036926	snp	C/T	0.0126979	0.078662	intron-variant	NEBL	GRCh38.p7	10:20965516	AAGGTCAAGGAAGGC[C/T]GCTCTGTCTGGAGCA	10529
rs78066637	snp	A/C	0	0	intron-variant	NEBL	GRCh38.p7	10:20967627	AGCGAGACTCCATCT[A/C]AAAAAAAAAAAAACA	10529
rs78068421	snp	C/T	0.0134861	0.0810011	intron-variant	NEBL	GRCh38.p7	10:20922913	CAAACACACAGAAAC[C/T]GATGACTTCAGGCAG	10529
rs78069317	snp	A/G	0.0174175	0.0916809	intron-variant	NEBL	GRCh38.p7	10:20996362	GTCATTTTCAACACT[A/G]ATCAATGTCACTTTA	10529
rs78074189	snp	A/G	0.0189856	0.0955633	intron-variant	NEBL	GRCh38.p7	10:21151671	CCCTTCCTCCTTTCC[A/G]CACAGGCTTCCTGCC	10529
rs78077945	snp	C/T	0.0189856	0.0955633	intron-variant	NEBL	GRCh38.p7	10:20903783	AAAAACCAAATACTG[C/T]ATGTTGTCTGTCACT	10529
rs78082104	snp	A/G	0.0535932	0.154675	intron-variant	NEBL	GRCh38.p7	10:20822549	GGTAGTAGTCTAACT[A/G]GATATAGAAAGACTA	10529
rs78104890	snp	C/T	0.0158469	0.0875917	intron-variant	NEBL	GRCh38.p7	10:21096981	CAAAAATCTCCAAGG[C/T]ATCCTTAAAAAAAAA	10529
rs78105141	snp	A/T	0.181022	0.240296	intron-variant	NEBL	GRCh38.p7	10:21119402	GTGTATATGTGCAGG[A/T]ATAAAGCAAATATTT	10529
rs78106113	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20973540	TAGACATAAGCCATC[G/T]CTCCCAGACTACCAT	10529
rs78123564	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20974682	ATTAACCTTTAATGG[C/T]TACACATACTACCAA	10529
rs78153109	snp	A/G	0.0325976	0.123435	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20860925	ATACAGCATTTGGTA[A/G]ATATTTTGAGATGGT	10529
rs78164859	snp	A/G	0.00755907	0.0610114	intron-variant	NEBL	GRCh38.p7	10:21102035	AAAATGTAGCATTCC[A/G]TTAAGGGCTTAATTA	10529
rs78181668	snp	A/G	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21053377	TCTGTGAGTCCCTGC[A/G]TACTCATCCACACTC	10529
rs78191737	snp	A/G	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:20828120	CCTCTTCCTCAAAAT[A/G]AAAATATAGAAGTTT	10529
rs78219874	snp	A/C	0	0	intron-variant	NEBL	GRCh38.p7	10:20951388	GAAGAAAATATGAGC[A/C]AAAAAAAAAAAAGAA	10529
rs78220302	snp	C/T	0.0221141	0.102801	intron-variant	NEBL	GRCh38.p7	10:20890429	GGGGATCACTATTAC[C/T]GTTATTACCTAGACA	10529
rs78222648	in-del	-/AAA			intron-variant	NEBL	GRCh38.p7	10:20976352	TAAAAAAAAAAAAAA[-/AAA]GTTTGGAGATTTCTC	10529
rs78227077	snp	A/T	0.00199481	0.0315187	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20865060	ACATGGGGGAATTTT[A/T]GTGGATTGAATTTGA	10529
rs78233073	snp	A/C	0	0	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20846495	AACGTGGATATAGCC[A/C]CAAGGAGAGAAACAA	10529
rs78237499	snp	A/T	0.0134861	0.0810011	intron-variant	NEBL	GRCh38.p7	10:20901855	TGGTATCTTCCCAGA[A/T]CAGAACTTTACTGAT	10529
rs78246976	snp	C/T	0.0158469	0.0875917	intron-variant	NEBL	GRCh38.p7	10:21116669	AATGCCTGGTAATTT[C/T]TTTTTCTTTTTACTT	10529
rs78275073	snp	A/G	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:21165347	CGTGAGACTATCCCA[A/G]CAGCAGGATACTTTA	10529
rs78286187	snp	A/G	0.0205511	0.0992634	intron-variant	NEBL	GRCh38.p7	10:20947864	CAGAAGTCTGCAATC[A/G]GACAATCTAACAAAC	10529
rs78288227	snp	A/C/G	0.0402882	0.136092	intron-variant	NEBL	GRCh38.p7	10:21010506	CCATCCTCCCACCTC[A/C/G]AACTCCCAAAGCACT	10529
rs78289343	snp	A/G	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20994882	TGAGGAGGAGGAGGT[A/G]GAGGGGGGGGTTGGT	10529
rs78341406	snp	A/T	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21170702	TTTTCTGATTTCTTG[A/T]AAAGTTTCTGGTCTA	10529
rs78344925	snp	G/T	0.0236746	0.106192	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20882232	AAGGAAAGAAAAAAG[G/T]AAGGAAGGAAGGAAA	10529
rs78370492	snp	A/G	0.0475351	0.146656	intron-variant	NEBL	GRCh38.p7	10:21036292	GACCTCCTTTCTACA[A/G]AAAATTCTCAAATTA	10529
rs78371009	snp	G/T	0.00597247	0.0543191	upstream-variant-2KB, intron-variant	C10orf113, NEBL	GRCh38.p7	10:21148121	CCTGTTGACAGTTGA[G/T]GCCTAAAGGACAAAA	10529
rs78373003	snp	A/G	0.000798403	0.0199641	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21130468	TCTTTTCAAACCCAC[A/G]TGAGACATTCACCAA	10529
rs78379893	snp	G/T	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20912903	TTTTTTTTTTTTTTA[G/T]ACAGAGTCTCTCTCT	10529
rs78392040	snp	A/G			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20872908	GAAATAACCATAACA[A/G]TGGGTAACCAGCAGC	10529
rs78401427	snp	A/T	0.0232847	0.105357	intron-variant	NEBL	GRCh38.p7	10:20900190	TTGGGCACTTCTTTT[A/T]TGTTGTTTACTTTTC	10529
rs78401567	snp	C/G	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21050934	ACACACCCTGTTTCA[C/G]TGACTTTCATCCTTT	10529
rs78402629	snp	A/T	0.0123036	0.0774623	intron-variant	NEBL	GRCh38.p7	10:20821516	ACAAATAACACCTAC[A/T]ATGTTATACTTTTTC	10529
rs78404089	snp	A/C	0.031825	0.122064	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20873095	TAGGTTTAAGGGAAG[A/C]TCATCTGACATTTCT	10529
rs78410682	snp	A/G	0.0271762	0.113356	intron-variant	NEBL	GRCh38.p7	10:21088635	GTAAATGGAAATACA[A/G]TCTACTATAATGACT	10529
rs78437737	snp	A/C	0	0	intron-variant	NEBL	GRCh38.p7	10:21160201	AAAGAAAAAAAAAAA[A/C]CTAATATGCTTTTCT	10529
rs78460358	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21046904	ACCGCGCCCGGCCCC[C/T]AACCTCAATATTTTT	10529
rs78464194	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21040337	GAGTAAGACTCCATT[C/T]AAAAAAAAAAGAAAG	10529
rs78476532	in-del	-/TGTAGAACCTCTGGTGTGTATGACAGGTCATGACATAGAACACTGCTTCAAGATTGAAACAGAAGCAGCATCTTTTTTCTCCCCGCTGAACTAGTT			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21131645	TTGTTTTCAAATCCA[lengthTooLong]ATTTCCTCCAACCAC	10529
rs78483041	snp	A/T	0.00874735	0.0655527	intron-variant	NEBL	GRCh38.p7	10:21159772	CACCTCCTAGACATG[A/T]TTCTCTTTTAGCATA	10529
rs78556338	snp	A/C	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20793573	TTTTTTTTTTTTTTA[A/C]CACAGGATCTGGCTC	10529
rs78557186	snp	A/C	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21075973	ATGCAAATCAAAACC[A/C]CAATGAGATACGACT	10529
rs78569554	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21064149	CTGTGTCTGTTGTTT[A/T]AATAATCACAGCAGT	10529
rs78574276	snp	A/G	0.077417	0.180873	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20874331	TTAGGCTGTCCTGCC[A/G]GATACCCCATCCATT	10529
rs78592181	snp	C/T	0.0737376	0.17729	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20847928	GTTGAAAATCAGGTC[C/T]GATTTGCTTCAGCCC	10529
rs78605337	snp	C/T	0.0158469	0.0875917	intron-variant	NEBL	GRCh38.p7	10:21095527	ATCACTAAACTGCTA[C/T]TTAAACTGTTAAGCT	10529
rs78608110	snp	A/T	0.0644693	0.167566	intron-variant	NEBL	GRCh38.p7	10:21016111	CATGCTATTTCTTTG[A/T]AGCAGTTCATGCTGG	10529
rs78608854	snp	A/C	0.0970103	0.197722	intron-variant	NEBL	GRCh38.p7	10:21026303	TGGTCAGGAGGCCAG[A/C]AATGAGGCTATCCTA	10529
rs78633885	snp	A/T	0.5	0	intron-variant, upstream-variant-2KB	NEBL, LOC102725112	GRCh38.p7	10:20844638	ATGTTTTTGGGGAAA[A/T]TTTTGCAGAGAATAA	10529
rs78641926	snp	A/G	0.0123036	0.0774623	intron-variant	NEBL	GRCh38.p7	10:21018359	ACCCTAACTTGACGA[A/G]AAGAAAGGCACATTG	10529
rs78648207	snp	C/T			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21130430	GTATAGACTACTTTA[C/T]CCAACAACAGCAGAA	10529
rs78689866	snp	C/T	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21074485	TCTGAATTTTTTTCT[C/T]TTTTTTTTTTTTGAG	10529
rs78714308	snp	A/G	0.0962929	0.197165	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20883278	CAGTCCTGCCCAGCC[A/G]TGTTCCTACCTCCAA	10529
rs78728646	snp	A/T	0.5	0	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20780643	GTGAACCATTTTTTT[A/T]ATATCCTGCATTTAT	10529
rs78753056	snp	C/T	0.0217236	0.101931	intron-variant	NEBL	GRCh38.p7	10:21124690	GAGCATAGTGGGTCA[C/T]AGCTGGAATCGCAGC	10529
rs78773557	snp	A/C	0.00716266	0.059414	intron-variant	NEBL	GRCh38.p7	10:20907912	AAAATACTGTTGTGC[A/C]GAATGATATTCAAGG	10529
rs78774958	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21026338	ACACTGTACAGCCCC[C/T]CCCTGACAGACTTAT	10529
rs78779479	snp	A/G	0.0729998	0.176553	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20875428	AGTTCTGGGTTAGAC[A/G]TGGCCAATAAGAGAA	10529
rs78782609	snp	C/T	0.0236746	0.106192	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20846626	CTTTCCTCTTCCTTA[C/T]GTGGAATTAGTAGAG	10529
rs78795009	snp	C/T	0.0205511	0.0992634	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21141230	TTAGTGAAATCTGAA[C/T]GAGGTCTGTAGATTA	10529
rs78797604	snp	A/G	0	0	intron-variant	NEBL	GRCh38.p7	10:20923843	CAGACCCTTGACTTA[A/G]AGCTCCTCATATCTA	10529
rs78806491	snp	C/T	0.154329	0.23097	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20781728	AAGCAACATACAATG[C/T]CTTGACTTTTTTGAT	10529
rs78837118	snp	C/G	0.0142736	0.0832652	intron-variant	NEBL	GRCh38.p7	10:21000687	TGCAAACAGAAATAA[C/G]GCTCCCAAAACGAGA	10529
rs78837996	snp	A/G	0.00716266	0.059414	intron-variant	NEBL	GRCh38.p7	10:20985540	AAAACTCATTACCAT[A/G]AAATCTCAATCTAAG	10529
rs78839771	snp	A/G	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:21023310	CAGAAAGTTTAGCCC[A/G]TTGAGAGATCCCCTT	10529
rs78855800	snp	C/T	0.0505692	0.150756	intron-variant	NEBL	GRCh38.p7	10:20825984	TAAAAAGCTTAGAGA[C/T]GTGACTGACATCGGT	10529
rs78867193	snp	A/G	0.030665	0.119967	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21143121	AATGTAGAAAAAGAG[A/G]AGTTTTCATAAACAT	10529
rs78889057	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21041424	GCAAAGACAACATCA[C/T]CATCACCACTAACAA	10529
rs78897325	snp	A/T	0.00874735	0.0655527	intron-variant, upstream-variant-2KB	NEBL, LOC102725112	GRCh38.p7	10:20844336	TTTCATATGTATGTA[A/T]GTAATATACATTCCG	10529
rs78899022	snp	C/T	0.0479149	0.147179	intron-variant	NEBL	GRCh38.p7	10:21026382	TCAACAGTGCTGAGG[C/T]TAATAAGTCTTGTTT	10529
rs78900586	snp	C/G	0.5	0	upstream-variant-2KB	NEBL	GRCh38.p7	10:21175933	AGAGCAAGAATGTTG[C/G]TGATATGTGACATTA	10529
rs78908479	snp	C/T	0.0023933	0.0345097	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20874194	ATTCTCCTATCTAAT[C/T]CCTTTGTAGTGGGCA	10529
rs78911131	snp	C/T	0.0240643	0.107019	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20871100	GTACAGTCATGGACA[C/T]TCTTAAAACCCATCT	10529
rs78937391	snp	C/T	0.00795532	0.062565	intron-variant	NEBL	GRCh38.p7	10:20930073	ACATTTATGCCTCTT[C/T]TCTGCCTTCTCCCCT	10529
rs78964235	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20921794	ACATGCACACACACA[C/T]ATATGTATACACACA	10529
rs78972282	snp	G/T	0.0310518	0.120672	intron-variant	NEBL	GRCh38.p7	10:21068160	TTTTTTCCTTCTTTT[G/T]ACAGATATTAATTAC	10529
rs78988959	in-del	-/CAAAA			intron-variant	NEBL	GRCh38.p7	10:21120680	AGTATTTCATGACAG[-/CAAAA]AAAAAAAAAAAAAAA	10529
rs78993744	snp	A/G	0.0402882	0.136092	intron-variant	NEBL	GRCh38.p7	10:21005333	ACCCCCAGCTGGTCA[A/G]ATTGGCCAGATTAGT	10529
rs79005415	snp	A/T	0.0134861	0.0810011	intron-variant	NEBL	GRCh38.p7	10:21051843	TATACAACTCAATGA[A/T]CACATTTGTTCCTTA	10529
rs79018643	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21121317	CACTTTAATGTCACG[G/T]TCATGCCAATCCCCG	10529
rs79020785	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21059190	GCACCCTGCACCTGC[A/G]TCTGTCATTGCTCTT	10529
rs79027451	snp	C/T	0.0232847	0.105357	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20855745	AAACTTTAATTAGAA[C/T]GATTTTACACAGTAA	10529
rs79062092	snp	A/T	0.046775	0.145601	intron-variant	NEBL	GRCh38.p7	10:21028472	CGCATGCACAGGCAC[A/T]CACACAAACACACAT	10529
rs79066944	snp	C/T	0.00874735	0.0655527	intron-variant	NEBL	GRCh38.p7	10:20991352	TGAAAATTTTTATGA[C/T]AGTGTTATAAACACT	10529
rs79069625	snp	A/G	0.0228947	0.104514	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21130557	TTCTCTCAGATCACA[A/G]TGAAATTAAACTAGA	10529
rs79071021	snp	A/T	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20898413	GCATAATTTTTTCTC[A/T]TGATATCATATCTAG	10529
rs79107431	snp	C/T	0.00755907	0.0610114	intron-variant	NEBL	GRCh38.p7	10:20826051	AATCCTTCACTTAAG[C/T]TGCCAAATAAATGTT	10529
rs79108668	snp	A/G	0.029116	0.117091	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20854201	GATAGCTGCTTATTA[A/G]ACAATGGGGTACCAG	10529
rs79109983	snp	A/C	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20980343	CCAGAACAAAAAGAA[A/C]AAAAAAAAAAGTTTC	10529
rs79143959	snp	A/G	0.0228947	0.104514	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20898916	TGTTGTGTTCTAGAA[A/G]GAGCTGTTGGTCTTG	10529
rs79145685	snp	C/T	0.0182019	0.0936463	intron-variant	NEBL	GRCh38.p7	10:20983584	CAAAATATCTGTCCA[C/T]AGGTATTCACAAGCA	10529
rs79148406	snp	A/G	0.0134861	0.0810011	intron-variant	NEBL	GRCh38.p7	10:20889172	CGTTTCTTTTCAAAC[A/G]TATCTCTTCTAAGTG	10529
rs79150812	snp	A/C	0.5	0	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20855524	AGAAAACAAAACAAA[A/C]CAAAAAAAAAACGAA	10529
rs79170499	snp	A/G	0.0414363	0.137845	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21128345	GGTTTTCTGCACTGG[A/G]TGAGTTAACCTAAAT	10529
rs79173137	snp	C/T	0.0741063	0.177655	intron-variant	NEBL	GRCh38.p7	10:21050571	CATGAGAACAATGAA[C/T]CAGCAGTAAAGCAAA	10529
rs79187684	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:20955339	GTGGTACAAATGATA[G/T]TGTTATAGCACAAAG	10529
rs79197535	snp	A/T	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20912898	TTTTTTTTTTTTTTT[A/T]TTTAGACAGAGTCTC	10529
rs79208256	snp	C/T	0.140242	0.224618	intron-variant	NEBL	GRCh38.p7	10:20947395	TTGTATGAGGGCAGG[C/T]TAGAAAGTGTCAAAC	10529
rs79210268	snp	C/T	0.0154538	0.0865337	intron-variant	NEBL	GRCh38.p7	10:21164032	TGCCCTATCTAGGTT[C/T]GACCAGAGAGGCCTG	10529
rs79224221	snp	A/T	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21095341	AAAGCAGATAAAAGA[A/T]AAGACGAACATGGTC	10529
rs79225043	snp	C/T	0.0228947	0.104514	intron-variant	NEBL	GRCh38.p7	10:20889495	ATCATTTATCTCTGA[C/T]ATATCTATTAGGAAA	10529
rs79245442	snp	C/G	0.00755907	0.0610114	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20850200	CCAATTCACCAATGA[C/G]AGAAGCTAAGGACCA	10529
rs79249696	snp	C/T	0.0170251	0.090679	intron-variant	NEBL	GRCh38.p7	10:20954551	ATGAAAATTCAGGCT[C/T]GCAGACAATTTGAAT	10529
rs79269131	snp	A/G	0.0166325	0.0896639	intron-variant	NEBL	GRCh38.p7	10:20908016	AAATGATGGGAGGCA[A/G]CCATGAAGTCTTCGA	10529
rs79272555	snp	A/G	0.0733688	0.176922	intron-variant	NEBL	GRCh38.p7	10:20838935	GTATGGTATAAACAT[A/G]ACATGTATATGTATG	10529
rs79274475	snp	C/T	0.0244538	0.107838	intron-variant	NEBL	GRCh38.p7	10:20842580	TAACTATTTTTTAAG[C/T]TAATTTTTAAAAAAT	10529
rs79301401	snp	G/T	0.0287284	0.116357	intron-variant	NEBL	GRCh38.p7	10:21023822	GTCTCTTCACTATGT[G/T]TGCACAAATTTCCTC	10529
rs79315402	snp	C/T	0.0154538	0.0865337	intron-variant	NEBL	GRCh38.p7	10:20948063	AAAGCTGTCCTGGGT[C/T]GCATGTGGCCCAAGG	10529
rs79328263	snp	C/T	0.0733688	0.176922	intron-variant	NEBL	GRCh38.p7	10:20838129	ATACATTTCATAGGG[C/T]TATACCTGTCATAGA	10529
rs79332448	snp	A/C	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21024083	GAAAAAAAAAAAAAA[A/C]ATTGAAAAGCTTCTA	10529
rs79340549	in-del	-/TT			intron-variant	NEBL	GRCh38.p7	10:20976336	GACTGAGACTCTATA[-/TT]AAAAAAAAAAAAAAA	10529
rs79356083	snp	A/G	0.0197687	0.0974348	intron-variant	NEBL	GRCh38.p7	10:20947820	AGGTAAGGGGCACCC[A/G]AAATAGAAAAGAATT	10529
rs79358035	snp	C/T	0.00795532	0.062565	intron-variant	NEBL	GRCh38.p7	10:20831092	AGAGTACACTAGCTC[C/T]GAATGCAATGCCCTC	10529
rs79386070	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21068764	AGGGAGAAGGAAAGC[C/T]TGAATATCTAAATAG	10529
rs79395726	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:20976764	ATAGACACTGGGGAC[A/T]TCAAAAGGGAGGAGG	10529
rs79410742	snp	C/G	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:21151431	ACAGTAAATATGTGA[C/G]TGTCCCTTTAGCACA	10529
rs79416472	snp	C/T	0.108048	0.20579	intron-variant	NEBL	GRCh38.p7	10:21063128	GCGGGTGCTCCATTG[C/T]TCAGAGGACTGAAAA	10529
rs79423213	snp	A/T	0.0271762	0.113356	intron-variant	NEBL	GRCh38.p7	10:20797574	TCAAGATACAGAAAT[A/T]CGAGAAAGTAAATGT	10529
rs79450707	snp	A/T	0.0614824	0.164198	intron-variant	NEBL	GRCh38.p7	10:20799950	GTGTGTGTGTGTGTG[A/T]GACGGAGAAAGAGAG	10529
rs79458098	snp	C/T	0.0422008	0.138995	intron-variant	NEBL	GRCh38.p7	10:20795176	TAGGAGTAAGAAGAC[C/T]GGATCTGAAGTTTGA	10529
rs79522691	snp	A/G/T	0.00119737	0.0244387	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21143866	GATAAGACAAGAAAA[A/G/T]AAAAAAAAAAAGCTT	10529
rs79561704	snp	C/T	0.0678174	0.1712	intron-variant	NEBL	GRCh38.p7	10:21007071	AAGAAAGGATAAACA[C/T]TTCAGTGGAGAATGA	10529
rs79562500	snp	A/T	0.5	0	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20959774	ACATTAAGACATCGC[A/T]AAAAGTTTTTTTTTT	10529
rs79563318	snp	A/C	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21024510	AGAATAAGATCTTCC[A/C]AAAAAAAAAAAAGAA	10529
rs79574302	snp	C/T	0.046775	0.145601	intron-variant	NEBL	GRCh38.p7	10:21043990	TCCTTTCTACAGATT[C/T]GTCTAAAAACAGGGT	10529
rs79580430	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21049307	TCCTATGAGGGTTGC[A/T]ACCATCTAGCAGGCC	10529
rs79585176	snp	C/T	0.0333695	0.124785	intron-variant	NEBL	GRCh38.p7	10:21098859	TCTAGCCAGGCATGG[C/T]GGCTCACACCTGTAA	10529
rs79621822	snp	A/T	0	0	intron-variant	NEBL	GRCh38.p7	10:20976340	GAGACTCTATATTAA[A/T]AAAAAAAAAAAAAAG	10529
rs79629357	snp	C/T	0.0189856	0.0955633	intron-variant	NEBL	GRCh38.p7	10:21117775	CTCAAATATCAACTT[C/T]AGAGAATCAGTTGAG	10529
rs79653691	snp	A/G	0.0722614	0.17581	intron-variant	NEBL	GRCh38.p7	10:21154015	TCAGAAATCTATTCC[A/G]CCTGATTCAGTGTTT	10529
rs79663677	snp	A/G	0.0244538	0.107838	intron-variant	NEBL	GRCh38.p7	10:20887578	TGCATGCCAACAAAC[A/G]GCTAATTTTTGTATT	10529
rs79688104	snp	C/T	0.0741063	0.177655	intron-variant	NEBL	GRCh38.p7	10:21053710	CAACATGAAGGGTCG[C/T]GTGTGAGTGTGATAA	10529
rs79692876	snp	A/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20891013	CCCTAATTATAACCC[A/T]AAAGTGGAGCTGAAT	10529
rs79694220	snp	A/T	0.5	0	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20851343	CCCAAGAGAAATTTT[A/T]CAAACTTAGAACTTT	10529
rs79703717	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20825676	CTCAAAAAAAAAAAA[A/G]AAACTCAATGTACTA	10529
rs79709336	snp	C/G	0.00597247	0.0543191	intron-variant	NEBL	GRCh38.p7	10:20908455	AACAAGCCCCCATGG[C/G]CGTTAGAAGCAACAG	10529
rs79718972	snp	C/T	0.0029818	0.0384969	intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20826455	AACTTACTGAACTAA[C/T]ATTCTGCTGATTTTT	10529
rs79727025	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21016845	GTATTACCATTAGGA[C/T]AGATACCTACCCACG	10529
rs79737221	snp	C/T	0.046775	0.145601	intron-variant	NEBL	GRCh38.p7	10:21025275	ATGTGGGGAATATGC[C/T]GAAATGTTTAGCATC	10529
rs79740314	snp	A/C	0.0228947	0.104514	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20898998	AACAAAATACCAAAA[A/C]GAAATTGCCTCAAGC	10529
rs79747119	snp	A/G	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21160860	TCAAACTTATTTCCA[A/G]GGGGAAAAAAAAAAA	10529
rs79747943	snp	A/G	0.00953873	0.0683987	intron-variant	NEBL	GRCh38.p7	10:21036637	CCAGGCTATTCAAAA[A/G]GTGCATTCAGATCAG	10529
rs79751788	snp	A/C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20943997	TTAATGAACAAGAGG[A/C/T]GGTTAAGTTTTGGAG	10529
rs79774471	snp	A/G	0.0158469	0.0875917	intron-variant	NEBL	GRCh38.p7	10:21170079	AATCAGATTGAACTC[A/G]AACTAAGCAATAAGC	10529
rs79776746	snp	A/G	0	0	intron-variant	NEBL	GRCh38.p7	10:21035374	ACAGTATGTGTTAAA[A/G]AAAATGAACTAAGCA	10529
rs79808256	snp	A/C	0.5	0	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21139987	GAAACCCTGTCTCAA[A/C]AAAAAAAAAAAAAAA	10529
rs79839401	snp	C/T	0.0138799	0.0821421	intron-variant	NEBL	GRCh38.p7	10:21164729	ATTAGATGTTGCCAA[C/T]GGTCCAATACGGTGA	10529
rs79863963	snp	C/G	0.00716266	0.059414	intron-variant	NEBL	GRCh38.p7	10:20904861	CAAGAGCCAGAAAGA[C/G]AGCAGGCTTGATCAC	10529
rs79872330	snp	A/G	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20952441	GACTCTGTCTGAAGG[A/G]AAAAAAAAAAAAAAA	10529
rs79906846	snp	C/T	0.0441095	0.141807	intron-variant	NEBL	GRCh38.p7	10:20805902	CATTATTTGAGTCAC[C/T]GAGTCATCGCTGCTG	10529
rs79919864	snp	G/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20867246	ACATTAACTTTGAAA[G/T]AGTTAACATTTTTTA	10529
rs79935982	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20824393	ATCTGTGGATTTCAT[A/G]TAAGTAACAATGCCA	10529
rs79961633	in-del	-/T	0.143622	0.226238	intron-variant	NEBL	GRCh38.p7	10:20968028	AGCCAAAGACTTGGG[-/T]TTTTTCGTAAATGGC	10529
rs80017829	snp	A/T	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20886372	TACTAAAAAAAAAAA[A/T]ACAAAAATTAGCTGG	10529
rs80018324	snp	A/G	0.0410537	0.137264	intron-variant	NEBL	GRCh38.p7	10:20814844	TTCTTCTAAGCAGCC[A/G]CAACTTAAAGGTAAT	10529
rs80020861	snp	A/C	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21024082	GGAAAAAAAAAAAAA[A/C]CATTGAAAAGCTTCT	10529
rs80026203	snp	A/G	0.0383715	0.133092	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20859141	AATCAATTTTTTGAT[A/G]TTGCTGTTTTTATAC	10529
rs80027810	snp	A/C	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20978754	AGCGAGACCCTATCT[A/C]AAAAAAAAAAAAAAG	10529
rs80034259	snp	G/T	0.0310518	0.120672	intron-variant	NEBL	GRCh38.p7	10:21152165	AGGAATGCAGGCGGA[G/T]TCAAGTCTGAGCTTA	10529
rs80045616	snp	A/C	0	0	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20868067	TAAAAAAAAAAAAAA[A/C]CGCTGTTGGAGTCTA	10529
rs80050390	snp	G/T	0.5	0	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20854633	GCAGTGGAGGGATCA[G/T]GGCTCACTGCAGCCT	10529
rs80053609	snp	A/G	0.0349115	0.127424	intron-variant	NEBL	GRCh38.p7	10:20906131	AAGGGAAATTCATTC[A/G]TATTATGTAGACCCT	10529
rs80057495	snp	A/T	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20924536	TATAAAAAAAAAAAA[A/T]AATCCCAGCAGGTAG	10529
rs80063760	snp	C/T	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21160202	AAGAAAAAAAAAAAA[C/T]TAATATGCTTTTCTT	10529
rs80087960	snp	A/G	0.0225045	0.103662	intron-variant	NEBL	GRCh38.p7	10:21158410	TTTATCCTTGCAGTA[A/G]CCAGAAGAGGTAGCA	10529
rs80088629	snp	C/T	0.00874735	0.0655527	intron-variant	NEBL	GRCh38.p7	10:20821979	CTAACTCCAACGTTA[C/T]CCCTTCCCCAAGGCT	10529
rs80123190	snp	A/G	0.0209421	0.100162	intron-variant	NEBL	GRCh38.p7	10:20933595	AAAAATTAGCCGGGT[A/G]TGGTGGCACGTGCCT	10529
rs80137388	snp	A/G	0.0240643	0.107019	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20878240	GCACAAGAGAGAGAC[A/G]TCTTGGTTCACTAAA	10529
rs80141802	snp	C/G	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20923867	ATATCTAGGAACCCA[C/G]CAGGAATAAAAGGAG	10529
rs80160833	snp	A/T	0.0150606	0.0854603	intron-variant	NEBL	GRCh38.p7	10:21159294	ATGACTAGACCAGTC[A/T]CAGGGGTATGGCACA	10529
rs80164320	snp	A/G	0.0228947	0.104514	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21129864	AAAAAATTTAAAATA[A/G]TAATAAATACGGCAG	10529
rs80169688	snp	A/G/T	0.00119737	0.0244387	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21143867	ATAAGACAAGAAAAG[A/G/T]AAAAAAAAAAGCTTA	10529
rs80170622	snp	C/G	0.0123036	0.0774623	intron-variant	NEBL	GRCh38.p7	10:20923890	AAAAGGAGGGGAGAG[C/G]TGGAGGATGAAACCC	10529
rs80182205	snp	A/C	0.0325976	0.123435	intron-variant	NEBL	GRCh38.p7	10:20810107	TATCTGTTAAGAAAT[A/C]TTTGTAATCAGATTG	10529
rs80186448	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20947578	AATCGATGGAGTAAT[C/G]TGCAAAAGTAAAACA	10529
rs80191733	snp	C/T	0.029116	0.117091	intron-variant	NEBL	GRCh38.p7	10:20991645	TATATTCAGGGGTAC[C/T]GGTGCAGTTTGTTAC	10529
rs80208855	snp	A/G	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:20886876	ACTATGTAAAAGGAA[A/G]CATATCCTTAGAAAG	10529
rs80215098	snp	A/G	0.0271762	0.113356	intron-variant	NEBL	GRCh38.p7	10:21085114	GACAAACCTACCAGC[A/G]ATTTTGAAAGAATTG	10529
rs80221462	snp	A/G	0.0475351	0.146656	intron-variant	NEBL	GRCh38.p7	10:21052431	TAACAATAAGACTCC[A/G]GAGAGCCTGGCAGCA	10529
rs80226645	snp	A/T	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20980400	AAAAAGAAAAAAAAA[A/T]ATATTTAGGTGCTTG	10529
rs80245404	snp	A/G	0.0486741	0.148216	intron-variant	NEBL	GRCh38.p7	10:21094807	GCTTCTAAGTCTCAC[A/G]TTGTAAAATTAATTT	10529
rs80246415	snp	C/T	0.00874735	0.0655527	intron-variant	NEBL	GRCh38.p7	10:20796736	CTCAGATTTGTTTCT[C/T]ATTTTATCTCTCTTA	10529
rs80254866	snp	C/T	0.0209421	0.100162	intron-variant	NEBL	GRCh38.p7	10:21054831	TACAATCATAGTATC[C/T]AAAAATGCCCAAATT	10529
rs80289095	snp	C/T	0.0333695	0.124785	intron-variant	NEBL	GRCh38.p7	10:21010151	GTTAATTTAATGAAA[C/T]GGGATTGCTTTAGAT	10529
rs80311269	snp	A/G	0.0225045	0.103662	intron-variant	NEBL	GRCh38.p7	10:21152389	TCCCAAAGTTATACA[A/G]TGCCCCTGGGCTATT	10529
rs80318171	snp	C/T	0.0562307	0.157967	intron-variant	NEBL	GRCh38.p7	10:20943278	AAATTGATGAGTTCA[C/T]GTCCTTTGTAGGGAC	10529
rs80318930	snp	C/T	0.00478085	0.0486577	intron-variant	NEBL	GRCh38.p7	10:20900077	AAAATCCCCTATCGA[C/T]TTTTCCAAAAACCAA	10529
rs80320329	snp	A/C	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:20980872	TTCCTTCTAACAGGC[A/C]AGAATTTAATATTCT	10529
rs80332707	snp	A/G			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20868053	CATTTTATCTATATT[A/G]AAAAAAAAAAAAAAC	10529
rs80333144	snp	G/T	0.158962	0.232835	intron-variant	NEBL	GRCh38.p7	10:20992055	ATGTCTTTGCCATTG[G/T]GAATGGTGCTGTGAT	10529
rs111075657	snp	C/T	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21061344	TTATGTGATATGTAA[C/T]ATGTTACATAATATA	10529
rs111236006	snp	C/T	0.0707826	0.174302	intron-variant	NEBL	GRCh38.p7	10:21097170	AATGAGCTCAATATC[C/T]GGCCAGGTGCGGTGG	10529
rs111239379	snp	C/T	0.0869089	0.189476	intron-variant	NEBL	GRCh38.p7	10:20900626	CTCAGGAGTTCGAGA[C/T]CAGCCTAGGCAACAT	10529
rs111243967	snp	C/T	0.0314385	0.121371	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21137999	GGAACTGGAAGTGGA[C/T]GGAGAGGAGCCCAGC	10529
rs111246152	snp	C/T	0.0365491	0.130703	intron-variant	NEBL	GRCh38.p7	10:20807222	ACCCACCTACTCAGG[C/T]GGCTGAGGCACAAGA	10529
rs111263479	in-del	-/C	0.464735	0.128019	intron-variant	NEBL	GRCh38.p7	10:21035327	TCTGATGCTCTCCTT[-/C]CCCCCGCCCCCCAAA	10529
rs111263742	in-del	-/ATA	0.0377422	0.132086	intron-variant	NEBL	GRCh38.p7	10:21017184	GTTACCTAAATAGAG[-/ATA]ATAATAAACACCTGT	10529
rs111265878	snp	A/C	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20807167	CCCGTCTCTATAAAA[A/C]ATACAAAAATTAGCT	10529
rs111270708	snp	A/G	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21074060	AGCCTGGGCGACAGA[A/G]TGAGACTCCGTCTCA	10529
rs111302888	snp	C/T	0.02016	0.0983543	intron-variant	NEBL	GRCh38.p7	10:21096190	AAGAAACAAACACTA[C/T]TGTGGACTTCAATAC	10529
rs111309876	snp	C/T	0.0115144	0.0749975	intron-variant	NEBL	GRCh38.p7	10:20811409	TCAGAACCCCTGCAC[C/T]ATCCCTTAAGATAGT	10529
rs111319540	snp	A/C	0.0718919	0.175435	intron-variant	NEBL	GRCh38.p7	10:21094032	AGCATCACTACTCAA[A/C]TTAATTTGTTCTTAT	10529
rs111332229	snp	C/T	0.0260105	0.111035	intron-variant	NEBL	GRCh38.p7	10:20829378	ACTCATAGGTGGGAA[C/T]TGAACAATGAGAACA	10529
rs111346650	in-del	-/T	0.478685	0.10101	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20784359	CAGCAAGGGCTAGCA[-/T]AAAGCCTGCAAAGTC	10529
rs111349591	snp	A/G	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20952934	AAAAAAAGAAAAAGA[A/G]AAAAGAAAAGAAAAG	10529
rs111353953	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20999082	TTGAATTATTTATTT[C/T]TATCTGCGGCACCAA	10529
rs111381594	snp	A/G	0.00517822	0.0506191	intron-variant	NEBL	GRCh38.p7	10:21004188	TACATTAAGAATGCA[A/G]TGGATATTTGGTAAC	10529
rs111416384	snp	G/T	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:21002357	CAGTCATCTAGCACT[G/T]ACTCACCACCTACTA	10529
rs111420847	in-del	-/A	0.252181	0.24999	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20898444	TTTTCAATGTACTGT[-/A]AAAAAAAAATGCCTT	10529
rs111427669	snp	G/T	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21000386	TGCTGCACTATGGTA[G/T]GGGGGATTCTGGTCC	10529
rs111431315	snp	C/G	0.00636936	0.0560724	upstream-variant-2KB, nc-transcript-variant	NEBL, NEBL-AS1	GRCh38.p7	10:21174869	CGACTGGTCATTTTA[C/G]GCCCGAGTCGAGCCT	10529
rs111439670	in-del	-/A	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21112412	ATACTATACAACCAT[-/A]AAAAAGTTGAGTTCA	10529
rs111442157	in-del	-/A	0	0	intron-variant	NEBL	GRCh38.p7	10:20979701	ACACAGTTTTTTTTA[-/A]TTCATTTATGTGTTT	10529
rs111452932	snp	C/T	0.5	0	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21126689	TAGAAGAAGCCTCCA[C/T]TGGGCCAGGTGCGGT	10529
rs111457062	snp	A/G	0.0115144	0.0749975	intron-variant	NEBL	GRCh38.p7	10:20919536	CCGATAGAATGAGAT[A/G]AACAGTCCAGAGATA	10529
rs111476721	snp	C/T	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21095207	AAGATTTCAGAACCC[C/T]TGCCCTGAAAGCTGA	10529
rs111480547	snp	A/G	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:20814318	TCTGTAAACCTGCGC[A/G]AGCCCGAGGACTCGT	10529
rs111494090	snp	A/G	0.0260105	0.111035	intron-variant	NEBL	GRCh38.p7	10:20819973	TCTGAGTTTGATCTT[A/G]TCAGTAATAATGAAT	10529
rs111507734	snp	A/C/G	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:21165959	TCAATCACCACTTCC[A/C/G]ATAAAAAATATTTTC	10529
rs111507858	snp	G/T	0.5	0	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21130369	AAATCAGCAAGGACA[G/T]AGTTGAATTCAACAC	10529
rs111513556	snp	A/G	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21087763	TGCAGCCCTGACCTC[A/G]GTATAATTGAGATTT	10529
rs111517338	snp	A/T	0.00438332	0.0466095	intron-variant	NEBL	GRCh38.p7	10:20796751	CATTTTATCTCTCTT[A/T]GGATAAACTCTGCAA	10529
rs111518365	snp	A/G	0.0126979	0.078662	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20854793	TGGTCTCAAACTCCT[A/G]GCCTCAAGCCATCCT	10529
rs111527824	snp	C/T	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:21013568	TTAGAAGTCTGAAGT[C/T]GTCCAATGAGATAAG	10529
rs111533005	snp	A/G	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20836222	GTTATGGTGCTTTGT[A/G]ATCAGTGATTTTTTT	10529
rs111556747	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20985963	TAAAAAGTTTAAAAA[C/T]ATATCCCTTTAGGTT	10529
rs111560687	snp	C/T	0.0670745	0.170406	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20855160	GCTTGAACCTGGGAG[C/T]GGAGGTTGCAGTGAG	10529
rs111563144	snp	A/G	0.5	0	intron-variant, downstream-variant-500B	NEBL	GRCh38.p7	10:20813581	AAACACACATTTTTA[A/G]AAACACAGCTTTAAA	10529
rs111569391	snp	C/T	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20796902	GTATATGTCTGTGTG[C/T]ACATGAACACGTGTG	10529
rs111577922	snp	A/C	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20826260	ATGAAACACTGCTTC[A/C]GAGTCAAGGGGAACA	10529
rs111579657	snp	G/T	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21072393	TCTTACTCCAAAGAG[G/T]GTCACATTCTGAGGT	10529
rs111581655	snp	C/T	0.5	0	intron-variant, upstream-variant-2KB	NEBL, LOC102725112	GRCh38.p7	10:20845597	GTAAATCATTCTAAG[C/T]GAGGCTTCCTAACAT	10529
rs111608296	in-del	-/T	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21001631	CAATATACTCACAAC[-/T]TTTTTTTTTTTTGTC	10529
rs111613814	in-del	-/A	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21071013	ACACTCTGCCTCTAC[-/A]AAAAAAAAAAGGAGC	10529
rs111620640	in-del	-/CGTCCCC	0.46014	0.13543	intron-variant	NEBL	GRCh38.p7	10:21029980	AGGTATAATGATAGA[-/CGTCCCC]CGTCCCCCTCAAAGA	10529
rs111621207	snp	A/C	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20816026	ACCCACCTCAGCCTC[A/C]CAAAGTGCTGGGATG	10529
rs111633784	snp	G/T	0.0134861	0.0810011	intron-variant	NEBL	GRCh38.p7	10:20948178	TGGAATTTAGAGTCT[G/T]TAATGGTTTGCATCT	10529
rs111648516	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21007547	TCTTTCTATTTCATT[C/T]CATACATTATCACCC	10529
rs111659741	snp	A/C	0.0486741	0.148216	intron-variant	NEBL	GRCh38.p7	10:21086503	CAGTGTCTAGTCGGG[A/C]ATGGTGGCTCACACC	10529
rs111661595	snp	C/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21109298	TTATGTGATGGATTA[C/T]GTTTATTGATTTGCG	10529
rs111665451	snp	A/G	0.00993419	0.0697739	intron-variant	NEBL	GRCh38.p7	10:20926702	GGGGGAGAGTGTGTC[A/G]TCTCGCATTCAGCAA	10529
rs111681971	snp	G/T	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:20938782	TCGCACAACAACTAC[G/T]TGACGAATGCACGAG	10529
rs111685230	snp	A/G	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:21114507	TTTGTTCTACCAATT[A/G]TCAAGAGTAAGGTGT	10529
rs111693100	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21090119	GCTCCAGGAGAATGG[A/G]AAGAATGAAAGTCCT	10529
rs111700349	in-del	-/A	0.161267	0.233723	intron-variant	NEBL	GRCh38.p7	10:20810368	AAAAACAAAACAAAC[-/A]AAAAAAAAAGTCCCT	10529
rs111709959	snp	A/G	0.0103295	0.0711199	intron-variant	NEBL	GRCh38.p7	10:20946267	GAAATTGGATTTTCA[A/G]ATAATCTTTTCATCT	10529
rs111722267	snp	A/G	0.0134861	0.0810011	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21136674	TGCTTTCTACCCTAC[A/G]GCTGGACAAAGCTCG	10529
rs111732038	snp	A/G	0.0115144	0.0749975	intron-variant	NEBL	GRCh38.p7	10:21076209	GCACTTTAGGAGGCC[A/G]AGGAGGGTGGATCAC	10529
rs111764557	snp	C/T	0.0349115	0.127424	intron-variant	NEBL	GRCh38.p7	10:20887492	GGCATGATCTTGGTT[C/T]GCTGCAGCCTCAACT	10529
rs111764914	snp	C/G	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:21155182	CCAGCCTCGGCGACA[C/G]AGCAAGACTCCCTCA	10529
rs111772740	snp	A/G	0.105924	0.204309	intron-variant	NEBL	GRCh38.p7	10:21062399	GGTGTAGTGGCTCTC[A/G]CCTGTAATCCCAGCA	10529
rs111787836	snp	A/G	0.0298908	0.118541	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20851970	ATATTTTATCTTAAC[A/G]GATGCTGGAACTGAC	10529
rs111789191	snp	C/T	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20796696	TTCTACATTTAGATT[C/T]GAATTGCCACTTCCA	10529
rs111805100	snp	C/T	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21046537	ATATGACTTTTCATT[C/T]GTTTTCTGCTTTAAA	10529
rs111805825	snp	C/T	0.00636936	0.0560724	intron-variant	NEBL	GRCh38.p7	10:21015165	TTCATTTTAAGCAGC[C/T]TTTTTCAAAACCATG	10529
rs111843659	snp	C/G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20827968	AGAAAAAATAACTAA[C/G/T]GGGTACTAGGCTTAA	10529
rs111848874	snp	A/G	0.0107246	0.0724382	intron-variant	NEBL	GRCh38.p7	10:21027440	TCAGGTGATCCTCCC[A/G]TCTCAGCCTCCTGAG	10529
rs111854914	snp	A/G	0.000576858	0.0169734	intron-variant, synonymous-codon, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20868724	TCTTCCAATTACAGC[A/G]GGCTCTTTATTCATT	10529
rs111859285	snp	C/T	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:21098405	ATCAATAAATGCTCA[C/T]TGAATTGAAATATGG	10529
rs111890733	snp	A/C	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20831747	ACTTGTGGTAGGAAT[A/C]CGACTTAGTATAACT	10529
rs111895045	snp	G/T	0.0185938	0.0946107	intron-variant	NEBL	GRCh38.p7	10:20910147	CTTTTCAGATGGATA[G/T]ATTTAGAAGAAATGA	10529
rs111897661	snp	C/G	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20906331	GGAATCCTTCTTCCT[C/G]AAATCATGATTTCAT	10529
rs111901646	snp	G/T	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21166465	AAACCTTTTAATAGG[G/T]GTGAGTGAGTTCTTA	10529
rs111931977	snp	A/T	0.00636936	0.0560724	intron-variant	NEBL	GRCh38.p7	10:20842687	GGAATAATTAAATCA[A/T]TCTAAATAATATATC	10529
rs111932157	snp	A/C	0.0244538	0.107838	intron-variant	NEBL	GRCh38.p7	10:21103788	AAGAAAAAGGTTTTC[A/C]TTTTCATAAAGTCAA	10529
rs111933179	snp	A/G	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20826374	AGCCATCAGTTGAGT[A/G]AAGAACTAAAAACAT	10529
rs111944506	snp	A/C	0.00716266	0.059414	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20859624	CAAATTACTTGGAAG[A/C]TAAGTATCAGTAATT	10529
rs111949309	snp	C/T	0.0349115	0.127424	intron-variant	NEBL	GRCh38.p7	10:21062398	TGGTGTAGTGGCTCT[C/T]GCCTGTAATCCCAGC	10529
rs111963054	snp	C/T	0	0	intron-variant	NEBL	GRCh38.p7	10:21055765	GTGACAAGCCTGTAG[C/T]GCAGATAATCCAGCC	10529
rs111995041	snp	C/T	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21037655	GTTTGTCAAAACTCA[C/T]AGAATCATATTCCAA	10529
rs111997042	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21098238	CACGTGCACACATAC[A/G]TACACACACTTGTAC	10529
rs111998215	snp	A/G	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20890430	GGGATCACTATTACC[A/G]TTATTACCTAGACAT	10529
rs112010030	snp	C/T			intron-variant, splice-acceptor-variant	NEBL	GRCh38.p7	10:20823301	TTCTTTGTATTTCAC[C/T]TGCATAATTTATAAG	10529
rs112013284	snp	C/T	0.0236746	0.106192	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20872317	AACAAGAGGACACCA[C/T]GGAGCCACACAGAAA	10529
rs112027371	snp	C/T	0.089084	0.191327	intron-variant	NEBL	GRCh38.p7	10:21109811	TATAGTATTTTCTGA[C/T]GGTAGTTTGTATTTC	10529
rs112033636	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20822373	TATAGGTCTATCTAT[A/G]GATAGATATCTATAC	10529
rs112059883	in-del	-/A	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20978755	GCGAGACCCTATCTC[-/A]AAAAAAAAAAAAAGT	10529
rs112063870	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20964611	ATCCAAACACCTCCC[A/G]TTAGTGCATACCTTC	10529
rs112069620	snp	G/T	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20999158	ACCCAGAGGTGTGTG[G/T]GGGGAAAAAAAAAAA	10529
rs112083950	snp	C/T	0.00993419	0.0697739	intron-variant	NEBL	GRCh38.p7	10:20932750	TTTGTCGATACTAAT[C/T]GTTGTGCTATTTCTT	10529
rs112099773	snp	C/T	0.0418186	0.138422	intron-variant, downstream-variant-500B	NEBL	GRCh38.p7	10:20817320	TGCAGTGAGTCAAGA[C/T]TGTGCCACTGCATTC	10529
rs112101379	snp	C/T	0.00795532	0.062565	intron-variant	NEBL	GRCh38.p7	10:21152138	GAGAAGGCAAGTCTT[C/T]CAGGGCCTGCGAGGA	10529
rs112107727	in-del	-/TG	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21057296	GGTAAGGCAGAGTAA[-/TG]TGTGTGTAAGTAGTA	10529
rs112117075	snp	C/T	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20931703	AGCCACCTGACATGA[C/T]ATGGACGAGGGTCTC	10529
rs112125167	in-del	-/TC	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21034959	TATTTATTTATTTAT[-/TC]TTATTTATTTATTTA	10529
rs112134201	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20784209	TTGTCATAGCTGTGA[A/G]GTCAGACCCTAAGTG	10529
rs112140504	snp	C/T	6.93001e-05	0.00588602	intron-variant	NEBL	GRCh38.p7	10:20889797	CTTTCATCTATATAA[C/T]AAGAAAAAGATAAAT	10529
rs112150815	snp	A/G	0.5	0	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20858479	TTACAAGGAGCCACT[A/G]GATGGTGCTGATTTA	10529
rs112152143	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21108580	GAGTGTTTTACTTCC[A/T]ATTATGTGGTCAATT	10529
rs112155930	snp	A/G	0.5	0	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21133728	TTTCCAAGGAAACCT[A/G]TGTCTCAAAATAATA	10529
rs112165628	snp	C/T	0.00914312	0.0669923	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20877281	TTACAGATGAGAAAA[C/T]GGAGATTTAGAGACA	10529
rs112166149	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20786902	CATGCTCCTAAGGCA[C/T]GAGTAAAGAGCATAA	10529
rs112171555	snp	A/G	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21069914	TGCAATTTTCCCCTG[A/G]TAGCGCAAGTCATGT	10529
rs112177736	snp	A/G	0.00199481	0.0315187	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21126868	TAATCCCAGCTACTC[A/G]GGAGGCTAAGGCAGG	10529
rs112196078	snp	A/T	0.00993419	0.0697739	intron-variant	NEBL	GRCh38.p7	10:20938338	AAACACGGTCTGGAG[A/T]GGACCTCCAGTAAAC	10529
rs112200276	snp	C/T	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21100659	TCTCCAAAAGAAATA[C/T]GACCTGATGGGCAAA	10529
rs112205494	snp	A/G	0.030665	0.119967	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21141002	TCCCATCAATAACGG[A/G]AACCCTGAATCTAAT	10529
rs112225028	snp	A/G			intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20809847	TGAATATTGTCTTCC[A/G]GGGGATCAAGGTCGA	10529
rs112236094	snp	A/G	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21052658	AAATGGCATGATCTT[A/G]AAAGAGCATGGATAA	10529
rs112244109	snp	C/G	0.121022	0.21416	intron-variant	NEBL	GRCh38.p7	10:21048936	AATTGCTTGAACCCG[C/G]GAGGTGGAGGTTGCA	10529
rs112271866	snp	C/T	0.0103295	0.0711199	intron-variant	NEBL	GRCh38.p7	10:20946440	TAGCTACGTGGCTAC[C/T]CATTTTATTATTTTT	10529
rs112298896	snp	A/G	0.0659589	0.169201	intron-variant	NEBL	GRCh38.p7	10:20807221	GACCCACCTACTCAG[A/G]CGGCTGAGGCACAAG	10529
rs112324891	snp	C/T	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20822209	CCTTGAGGATGCCCA[C/T]GACCCCTAATCTCAG	10529
rs112335697	snp	C/T	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21118390	CAGACATTGACTCCA[C/T]TTTACATTTAGTCTA	10529
rs112339267	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21032645	AAGCAGACTTATGAG[A/C]GCTGCTGATAGATAA	10529
rs112340187	snp	A/G	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21171350	CAAAAAAAAAAAAAA[A/G]AAAAAAAAAAAAGAA	10529
rs112356472	snp	A/G	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21067034	CTGTAGTGCAGTGGC[A/G]CGATCTCCACTCACT	10529
rs112376824	snp	C/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21109304	GATGGATTATGTTTA[C/T]TGATTTGCGTATGTT	10529
rs112383189	snp	C/T	0.0376037	0.131863	intron-variant	NEBL	GRCh38.p7	10:21093700	GTATCCACAGATCTC[C/T]GTCTTGTTCAGGTAT	10529
rs112386700	snp	A/C	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21095127	TCATCTCAGACCAAC[A/C]AACCATATCAGAATC	10529
rs112404095	snp	C/T	0.0103295	0.0711199	intron-variant	NEBL	GRCh38.p7	10:20944195	ACCTGAGGTCTGGAG[C/T]TCAAGACCAGCCTTG	10529
rs112412276	snp	C/G	0.5	0	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21131293	TAGATTAGTTCACTG[C/G]TGAAGTCTACCAGAC	10529
rs112412623	snp	A/C	0.0256215	0.110247	intron-variant	NEBL	GRCh38.p7	10:20823005	ATAATATGTGTCTTT[A/C]ATAAATAAATGCTGA	10529
rs112414379	snp	C/T	0.000153988	0.00877328	intron-variant	NEBL	GRCh38.p7	10:20831178	ACACGATTCTGAGCA[C/T]CTTCATTCATGACCA	10529
rs112419366	snp	C/T	0	0	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20860287	TTTCCTATACTTCAT[C/T]TGCTCAAAAATTTAG	10529
rs112438326	snp	C/G	0.00119737	0.0244387	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20784337	TGGATGAAATTTCAA[C/G]ACCCACCAGCAAGGG	10529
rs112475831	snp	A/G	0.00279162	0.0372561	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21144444	ATAAAATCAGAATGG[A/G]GCCGGGTGCTGTGGC	10529
rs112479393	in-del	-/A	0.0681886	0.171594	intron-variant	NEBL	GRCh38.p7	10:20994884	AGGAGGAGGAGGTAG[-/A]GGGGGGGGTTGGTCT	10529
rs112483616	in-del	-/TAA	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21005745	AAACAATAATAATAA[-/TAA]TAAATTAAATAAAAT	10529
rs112495822	in-del	-/A	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21034003	AAAACTCATCTCTAC[-/A]AAAAAATACAAAAAT	10529
rs112496684	in-del	-/A	0.0341777	0.126177	intron-variant, upstream-variant-2KB	NEBL, NEBL-AS1	GRCh38.p7	10:21172482	TTATGCCAATACTGG[-/A]AAAAAAAAAAAAACA	10529
rs112501572	snp	C/T	0.5	0	intron-variant, downstream-variant-500B	NEBL	GRCh38.p7	10:20815336	AAGGCTTTACCACCT[C/T]CAAAGACACGGCTAA	10529
rs112511628	snp	A/T	0.00993419	0.0697739	intron-variant	NEBL	GRCh38.p7	10:21043869	TCTATTATAAAATTT[A/T]AAAAGTTGCCAATTC	10529
rs112513911	snp	C/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20831848	AAGGGGAAAATTTAA[C/G]ATTTCAATATGATAA	10529
rs112519422	snp	G/T	0.00953873	0.0683987	intron-variant	NEBL	GRCh38.p7	10:21071474	ATTTTGCTGAGTCTT[G/T]GTTTTCTTATCTGCA	10529
rs112545336	snp	C/T	0.5	0	intron-variant, synonymous-codon, nc-transcript-variant	NEBL	GRCh38.p7	10:20828542	CACCGCACTAATGTT[C/T]TGTTGAGTTGTCTTA	10529
rs112547163	snp	C/T	0.0505692	0.150756	intron-variant	NEBL	GRCh38.p7	10:20836371	GGGACTACAGGCATG[C/T]GCCACCACATCCAGC	10529
rs112558295	snp	A/G	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20840430	CTGCAGTTACTGATG[A/G]ACCATAATAACATAC	10529
rs112559213	snp	C/T	0.0103295	0.0711199	intron-variant	NEBL	GRCh38.p7	10:20990983	ATTTTGCACGCTGTC[C/T]ATCAATCAAGCTCTG	10529
rs112570699	snp	A/C	0.0170251	0.090679	intron-variant	NEBL	GRCh38.p7	10:20954777	ACCCTAGTGGGCAGG[A/C]TGGTTGGAGTTTTTC	10529
rs112589914	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21106698	CCATATGAACTTTAA[A/T]GTAGTTTTTTCCAAT	10529
rs112622575	snp	C/T	0.0228947	0.104514	intron-variant	NEBL	GRCh38.p7	10:20932564	CCTGCACATTCTGCA[C/T]ATGTATCCCAGAACT	10529
rs112634254	snp	C/T	0.0134861	0.0810011	intron-variant, downstream-variant-500B	NEBL, LOC102725112	GRCh38.p7	10:20880242	GGTGGGCACCTGTAA[C/T]CCCAGCTACTCGGGA	10529
rs112640716	snp	C/T	0.0505692	0.150756	intron-variant	NEBL	GRCh38.p7	10:21075330	TAAAATGGCTGGAGA[C/T]GGACTGAGAGGGTCA	10529
rs112664806	snp	A/T	0.5	0	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20862976	CAGTGCATAATAATC[A/T]CATCAGGGAAATAAC	10529
rs112679780	snp	A/G	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20903692	AACTCAGGCAGAAAA[A/G]GAACAAAATAACGTA	10529
rs112685548	in-del	-/AAGAG	0	0	intron-variant	NEBL	GRCh38.p7	10:21095334	CTAAGAAAAGCAGAT[-/AAGAG]AAAAGATAAGACGAA	10529
rs112689549	snp	C/T	0.0494327	0.149241	intron-variant	NEBL	GRCh38.p7	10:21073482	ATTAGGCAGGCTTGG[C/T]GGCACGCACTTGTAA	10529
rs112700976	snp	C/T	0.5	0	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21130657	GTTCAAAGAATAAAT[C/T]TCAAGATAAATTATA	10529
rs112701084	snp	A/G	0	0	intron-variant	NEBL	GRCh38.p7	10:21150294	AAGCTTTCGCTTCTC[A/G]TCAACTTTCTGACAA	10529
rs112701521	snp	A/C	0.0248432	0.108648	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20785662	GTAAAATAATGGCCA[A/C]GTTGTCTTAAAAGTA	10529
rs112715564	snp	A/G	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20814062	CAAAGTAAATAGTAG[A/G]CATAAGACAATGATA	10529
rs112739062	snp	A/G	0.5	0	intron-variant, upstream-variant-2KB	NEBL, NEBL-AS1	GRCh38.p7	10:21173392	GGATCTGTGGGGCGG[A/G]GGGCGGGGGTATTGT	10529
rs112740535	snp	A/C	0.5	0	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20883205	TCCACGGACCACAAC[A/C]TTTTTCTTTTGATGG	10529
rs112743242	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21061003	GATTTGTTGAAGTCC[C/T]AACACCAGGTGCCTG	10529
rs112757413	in-del	-/CA	0.375	0.216506	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20852541	GTACGGGCAAGTGTG[-/CA]TACCTGACTTTGGAG	10529
rs112771870	snp	A/C	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20810372	AACAAAACAAACAAA[A/C]AAAAAGTCCCTTTCT	10529
rs112774637	snp	C/T	0.00914312	0.0669923	intron-variant, downstream-variant-500B	NEBL	GRCh38.p7	10:20817391	AAAAGAAAAAAGTCA[C/T]CCTGATGAGTCACTG	10529
rs112796520	snp	C/T	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:21049560	TTGTTCTCCCACCCA[C/T]CTATTTATTGAAATC	10529
rs112828630	snp	A/G	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20830407	TATTTGCTAATGAAT[A/G]TTTTTGCCCAAGTCA	10529
rs112846574	in-del	-/GTTTTTT	0.245061	0.249951	intron-variant	NEBL	GRCh38.p7	10:20989291	CTTTACTTTGGGGAG[-/GTTTTTT]GTTTTTTGTTTTTGT	10529
rs112848303	snp	A/G	0.0314385	0.121371	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21145783	AAGGCTAACCTGCAC[A/G]CAAACCCTGTAGGGA	10529
rs112851298	snp	C/T	0.0490535	0.14873	intron-variant	NEBL	GRCh38.p7	10:21086499	AAATCAGTGTCTAGT[C/T]GGGCATGGTGGCTCA	10529
rs112853221	in-del	-/TCTT	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21122055	TTTTGAGACACAGTC[-/TCTT]TCTATCACCCAGACT	10529
rs112869184	snp	C/T	0.164219	0.234823	intron-variant	NEBL	GRCh38.p7	10:20968472	GCTATGTTCACACCA[C/T]TGCACTCCAGCCTGG	10529
rs112872486	snp	C/T	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20920355	ATACAAGACTATTCA[C/T]TACAATACTAGCAAT	10529
rs112874134	snp	C/G	0.0260105	0.111035	intron-variant	NEBL	GRCh38.p7	10:20823730	GTCTGGGGAGCACTG[C/G]TTGTCTGACTGAGAG	10529
rs112883469	snp	A/G	0.00358779	0.0422022	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20884091	AACCTGGAGACAGGA[A/G]TCCACTTGCAATAGT	10529
rs112886429	snp	A/G	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21097577	TTTGTATATTGCCAG[A/G]CCCTGGGCTCTGCCT	10529
rs112913690	snp	C/T	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20799015	ATGAACGAATACTTG[C/T]GAACAATGTACAATG	10529
rs112916267	snp	C/T	0.00914312	0.0669923	intron-variant	NEBL	GRCh38.p7	10:21117900	TATCTAACCTGAGTC[C/T]ACCTGATCTATAAAA	10529
rs112919813	snp	C/G	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21100946	TTTGTTTGTTTTAAT[C/G]GAAGTTTCCATTCCC	10529
rs112934765	snp	C/T	0.0325976	0.123435	intron-variant	NEBL	GRCh38.p7	10:20928594	GGGTGTCTCACTTTC[C/T]CCTGCCCAAAACTGT	10529
rs112957077	snp	G/T	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21057626	GTGAACTTGGCTCAC[G/T]GCAACCTCTGCCTCC	10529
rs112971260	snp	A/T	0.0629771	0.165899	intron-variant	NEBL	GRCh38.p7	10:21166098	GGTGGCGGGCGCCTG[A/T]AGTCCCAGCTACTCC	10529
rs112975180	snp	A/G	0.0248432	0.108648	intron-variant	NEBL	GRCh38.p7	10:20938571	CTCCTCACCAACAAC[A/G]GAACAAAGCTGGATG	10529
rs112978628	snp	C/T	0.00953873	0.0683987	intron-variant	NEBL	GRCh38.p7	10:21076345	AGCTACTCAGAAGGC[C/T]GAGGCAGGAGAATCG	10529
rs112981415	snp	A/G	0.0178098	0.0926698	intron-variant	NEBL	GRCh38.p7	10:20815833	AAGTGCAGTGGTACA[A/G]TCTTTGCTCACCACA	10529
rs113012374	snp	A/G	0.0103295	0.0711199	intron-variant	NEBL	GRCh38.p7	10:20946692	CTGGTCTCAAACACC[A/G]CGCCAGTCCCGTTTT	10529
rs113026151	in-del	-/AAAACAA	0.248755	0.249997	intron-variant	NEBL	GRCh38.p7	10:21054033	GCAAGACTCCATCTC[-/AAAACAA]AAAACAAAAAACAAA	10529
rs113040664	snp	A/T	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21010129	GGAATAGTTCCCTAA[A/T]GAGCCTGTTAATTTA	10529
rs113041537	snp	A/T	0.0479149	0.147179	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20859077	GATCAATAATACATA[A/T]TTTTTATACTTGAGA	10529
rs113043384	snp	A/G	0.0260105	0.111035	intron-variant	NEBL	GRCh38.p7	10:20822279	CAGAGAAGACATTCA[A/G]TAACACATTTCATGT	10529
rs113043946	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20840913	TTCAGTGTGCTATTC[C/T]ACATGTTTTCTAGAG	10529
rs113053520	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20974759	ACTACTTAAAATGAC[C/T]TGTAAAATAACTGCA	10529
rs113067010	snp	G/T	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20799893	AAATGGTTACTATAG[G/T]GAAGCAAATTATCAT	10529
rs113071729	snp	A/C	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20788291	GTAAAACTTATAGTC[A/C]TATGTGCTATAAAAT	10529
rs113083361	snp	C/G	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20823075	TGTGTAAAATGCTAG[C/G]TCCACTTTTAAGGAA	10529
rs113095160	snp	A/G	0	0	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20860386	AATTCCACTAAATTC[A/G]GCAGGAAAACCATCT	10529
rs113108680	snp	G/T	0.00597247	0.0543191	intron-variant	NEBL	GRCh38.p7	10:21026258	TCATTTGGGAGTGAG[G/T]AGGGAGGGGAAAATA	10529
rs113112162	in-del	-/A	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20820824	GTAAGACTCTATCTC[-/A]AAAAAACAAAACAAA	10529
rs113113534	snp	C/T	0.0221141	0.102801	intron-variant	NEBL	GRCh38.p7	10:20949369	TTAAAACCTAGGTGA[C/T]GGATTGATAGGTACA	10529
rs113117610	in-del	-/AG/GA	0.463126	0.13068	intron-variant	NEBL	GRCh38.p7	10:21033753	CCGAAAAAAAAAAAA[-/AG/GA]AAAGAAAGAAAAGAA	10529
rs113131794	snp	A/T	0.0217236	0.101931	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20851839	AATTTTTAGAAATGA[A/T]GTATATTTCCAAACT	10529
rs113149472	in-del	-/G	0.376195	0.215812	intron-variant	NEBL	GRCh38.p7	10:21005505	TTGCAAGGTCAAGAT[-/G]GGGGGGATCGCTTGA	10529
rs113154945	snp	C/G/T	0	0	splice-donor-variant	NEBL	GRCh38.p7	10:20787201	TCAAATGGACACTTA[C/G/T]TAGATTTGGTGAATG	10529
rs113157938	snp	G/T	0.0142736	0.0832652	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20874755	CATTTTTTTTCTTTT[G/T]TGAAGATGAAGTCTT	10529
rs113167743	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20826316	TAGATCTTTGATATA[C/T]GATGAAATAGCATTT	10529
rs113179128	snp	A/G	0.00953873	0.0683987	intron-variant	NEBL	GRCh38.p7	10:20964801	GGCAAGCAAAAGAGT[A/G]ATTGAGAGAGAGTCC	10529
rs113210711	snp	C/T	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21158545	GGCAAAGTAACTCAA[C/T]GTCAGCCCCAGAAGG	10529
rs113238784	snp	C/T	0.00914312	0.0669923	intron-variant	NEBL	GRCh38.p7	10:21093723	TCAGGTATATCTAAG[C/T]TCATCCACTGGAAGA	10529
rs113241460	snp	C/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20791588	TCCCTACAGACAGGA[C/T]CTTGCTACATTGCCC	10529
rs113263429	snp	A/G	0.5	0	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20858453	ATTTAGTGGTAAATG[A/G]ACAGACGAATTTACA	10529
rs113279397	snp	A/C	0.0244538	0.107838	intron-variant	NEBL	GRCh38.p7	10:20924839	TTAGTTAACCATAAT[A/C]CGGCTGGCGCTATAA	10529
rs113307055	snp	C/T	0.0879971	0.190408	intron-variant	NEBL	GRCh38.p7	10:20894998	TAGTACATTCTACCA[C/T]GCCACAAAAATCTGT	10529
rs113310195	in-del	-/A	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20970648	GCGAGACCTCATCTT[-/A]AAAAAAAAAAAATTA	10529
rs113316961	snp	C/T	3.30486e-05	0.00406487	intron-variant, splice-donor-variant, utr-variant-3-prime	NEBL	GRCh38.p7	10:20815624	GAAGAAAACCACTTG[C/T]CGAGCTAATATTTTC	10529
rs113325859	snp	C/T	0.084728	0.187577	intron-variant	NEBL	GRCh38.p7	10:21067901	GGAGGATCACTTGAG[C/T]GCAGGAGGTCAAGGC	10529
rs113359337	snp	A/G/T	0.0107367	0.0726029	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20876612	TCTTTCATTTCCCAC[A/G/T]CTGAATACTTCTTTC	10529
rs113370481	snp	C/T	0	0	intron-variant	NEBL	GRCh38.p7	10:20977558	AGCTGGCCTGTGAGC[C/T]CACAGGAGGAGGAGG	10529
rs113372903	snp	A/G	0.00993419	0.0697739	intron-variant	NEBL	GRCh38.p7	10:20991690	TGATGCAGAGGTTTG[A/G]GCTTTTAATGACCTC	10529
rs113378754	snp	A/C	0.0146672	0.084371	intron-variant	NEBL	GRCh38.p7	10:20916526	ACTCTCCTACCTCAG[A/C]CTCCCAAGTAGCTGG	10529
rs113380076	snp	G/T	0.0134861	0.0810011	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20869287	ACTAAAGCGGGCACC[G/T]TAGAGAAGGTAAGAA	10529
rs113384071	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20783705	TAAATATATACTTAG[C/T]AAAATAAAATTGAGC	10529
rs113394390	snp	A/C	0.0633504	0.166319	utr-variant-5-prime, upstream-variant-2KB	NEBL, NEBL-AS1	GRCh38.p7	10:21173940	CAGGCGGGAGGGCTG[A/C]GGGCGGCGGGCGCCG	10529
rs113404858	in-del	-/A	0.298651	0.24522	intron-variant	NEBL	GRCh38.p7	10:20900669	TCTCTACTAAAATAC[-/A]AAAAAAAAAAAAAAA	10529
rs113405517	snp	C/T	0.0678174	0.1712	intron-variant	NEBL	GRCh38.p7	10:21008159	TGTATAGGTAGATGT[C/T]ATACAAATGTATGTA	10529
rs113406843	snp	C/T	1.71361e-05	0.00292707	intron-variant, synonymous-codon, nc-transcript-variant	NEBL	GRCh38.p7	10:20828530	GTAATGGCTACTCAC[C/T]GCACTAATGTTTTGT	10529
rs113407871	snp	A/C	0.00874735	0.0655527	intron-variant	NEBL	GRCh38.p7	10:20979410	ATGAAAGAGAAGATG[A/C]AAAAGGTGGTCAAGA	10529
rs113408801	snp	C/G	0.00533576	0.0513752	intron-variant	NEBL	GRCh38.p7	10:20817740	GCACAATGGGCTCCA[C/G]TGAAATACCACAAAG	10529
rs113419832	snp	C/G	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21003320	GGAAACAGCTTTATG[C/G]ATTAAGCTCACACTT	10529
rs113435169	snp	A/T	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20999578	CACTCCAGCATGGGC[A/T]ACAGAGTGAGACCCT	10529
rs113451828	snp	A/G	0.00014872	0.00862193	synonymous-codon, intron-variant, utr-variant-3-prime	C10orf113, NEBL	GRCh38.p7	10:21125859	CACCTTCTTAGATAC[A/G]TTGAACTTTTCTTTT	10529
rs113453202	snp	A/G	0.101301	0.200969	intron-variant	NEBL	GRCh38.p7	10:20992801	TTTTTTTTTTGAGGC[A/G]GAGTCTCGCTCTGTC	10529
rs113459292	snp	A/C	0.00636936	0.0560724	intron-variant	NEBL	GRCh38.p7	10:21166936	TAGATGGTGGGAATA[A/C]TCTCAGGTTTCAATT	10529
rs113464107	in-del	-/ATAA	0.463774	0.129618	intron-variant	NEBL	GRCh38.p7	10:21037824	ATGAAGAGTAGAAAG[-/ATAA]ATAGACAAAATGAGA	10529
rs113465582	snp	A/G	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:21073238	TGAAGCAGGGGGATC[A/G]GTTGAGCCCAGGAGT	10529
rs113475213	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:20944260	CAAAAATTAGCCAGG[C/G]CTGGTGACGGGTGCC	10529
rs113491557	in-del	-/A/AA	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21007111	CCGAATGAAATACAG[-/A/AA]AAAAAAAAAACTGTT	10529
rs113515307	snp	A/C	0.0185938	0.0946107	intron-variant	NEBL	GRCh38.p7	10:20912070	TTACGGTTATAATAA[A/C]TTTTCTTATTCTTCA	10529
rs113525323	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20808998	ACTATCACCAGATAT[A/G]TAGTATGTGTTGCCT	10529
rs113584021	in-del	-/C	0.0236746	0.106192	intron-variant	NEBL	GRCh38.p7	10:21024660	CAATATCTGTAGGAA[-/C]CTAATTAATTTCAAA	10529
rs113585500	snp	A/T	0.0402882	0.136092	intron-variant	NEBL	GRCh38.p7	10:21005824	TACAATGAATTACTG[A/T]CATACTAACACTTTT	10529
rs113589758	snp	C/T	0.097727	0.198275	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20851497	ACTTTGTGAAATGGC[C/T]GGGTGCAGTGGCTCA	10529
rs113590560	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20974043	ACTTTTATCACTTGT[A/G]ACCAAGAATTCTAAC	10529
rs113599360	snp	A/C	0.0170251	0.090679	intron-variant	NEBL	GRCh38.p7	10:20893105	CTAAACAGCCTTGAA[A/C]TAAACACTGAGAGGC	10529
rs113604229	snp	A/G	0.0298908	0.118541	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21144669	GAGTTGGAGGTTGCA[A/G]TGAGCCGAGATCATG	10529
rs113607194	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20803831	TATATATATATATAT[A/C]TATATATGCACACAT	10529
rs113613364	in-del	-/TG	0.438386	0.164349	intron-variant	NEBL	GRCh38.p7	10:20795560	AGTGTGCGTGTGCAA[-/TG]TGTGTGTGTGTGTGT	10529
rs113615067	snp	C/T	0.0252325	0.109451	intron-variant	NEBL	GRCh38.p7	10:20786366	ACTATGTAAAACAAA[C/T]GAAAGAAAAAACTCA	10529
rs113627047	snp	C/G	0.0376037	0.131863	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20864893	CTTGTGAGTTTTATA[C/G]AGCTTATAAAATCTT	10529
rs113640261	snp	A/G	0.0236746	0.106192	intron-variant	NEBL	GRCh38.p7	10:20830908	GACCTCCATCTCTAA[A/G]ATTTAAAAAAAAAAA	10529
rs113644293	in-del	-/A	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21070630	AACCAAGACACACTT[-/A]AAAAAAAATTACTCT	10529
rs113647668	snp	A/G	0.0626037	0.165477	upstream-variant-2KB, nc-transcript-variant	NEBL, NEBL-AS1	GRCh38.p7	10:21174696	GGAGACCTGCGTCCC[A/G]GAGGGGCCGAGGGTT	10529
rs113650237	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20840674	TAGAACCTTTGAGAA[A/G]GATTGACAAATAAGA	10529
rs113653793	snp	C/G	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20998988	TATGCTGGGTGTTCA[C/G]GGTTAGGCAAGGCCT	10529
rs113660269	snp	A/G	0.0154538	0.0865337	intron-variant	NEBL	GRCh38.p7	10:20938834	ACTGGAAGAAAGGAT[A/G]TCAGTGATGCAACAT	10529
rs113675805	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:20900981	CAAGATCGCGCCACT[G/T]CACTCCAGCCTGGGT	10529
rs113678622	snp	C/G	0.5	0	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21128501	TTGATTACTGTATCA[C/G]ATTAAATTTAATCTA	10529
rs113697310	snp	G/T	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21111317	AAGAACAAAGTGGGA[G/T]GCATCGTGCTACCTG	10529
rs113729422	in-del	-/T	0.0524604	0.153226	intron-variant	NEBL	GRCh38.p7	10:21151713	CCCACACGCCCCAGG[-/T]TTCACTCCGTGCCCT	10529
rs113743677	snp	C/G	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20963228	TCACCCTCCATCTCC[C/G]AGCATGGGTAAAGAT	10529
rs113747484	snp	C/T	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21169984	GGGCCCACATCTCAA[C/T]GTTTCTGGGCACTCA	10529
rs113762795	snp	C/T	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21108398	AAGAACATCTTTATT[C/T]CTGCCTTCGTTTCAT	10529
rs113763844	snp	A/C/T	0	0	splice-donor-variant	NEBL	GRCh38.p7	10:20787200	ATCAAATGGACACTT[A/C/T]CTAGATTTGGTGAAT	10529
rs113790766	in-del	-/A	0.276534	0.248588	intron-variant	NEBL	GRCh38.p7	10:20978431	CAAGAAAAGCTAACC[-/A]AAAAAAAAAACGAGT	10529
rs113792293	snp	A/G	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21056098	GCTCTGACACAGGCT[A/G]GACACTAGGTCAGAT	10529
rs113798484	snp	C/T	0.162909	0.23434	intron-variant	NEBL	GRCh38.p7	10:20829244	ATATACACCATGGAA[C/T]ACTATGCAGCCATAA	10529
rs113812586	snp	C/T	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:21108743	TGTCTCATTGATCTG[C/T]CTAATATTAGCAGTG	10529
rs113830620	snp	A/G	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21115811	GTTCCTTCCCAATCC[A/G]CTCTTAATTTTTTAG	10529
rs113833271	snp	C/G	0.0310518	0.120672	intron-variant	NEBL	GRCh38.p7	10:21155916	TGCATGACAAGAACA[C/G]AGGCCCCAAGAGGTG	10529
rs113833790	snp	A/G	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21121771	CCCTAATTGACAGTA[A/G]CACATTAGACAGCCT	10529
rs113848122	snp	A/G	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21112615	ACTGGGGGAGGGATA[A/G]CATTAGGAAAATACC	10529
rs113853425	snp	C/T	0.5	0	intron-variant	NEBL	GRCh38.p7	10:21058596	AAAGAAACAACATTA[C/T]TTAATGGCATGTTTA	10529
rs113873684	snp	A/C	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21068641	GGCTCTGGTCTTTTC[A/C]GCTGTCAGCTACTAA	10529
rs113881821	in-del	-/A	0.0252325	0.109451	intron-variant	NEBL	GRCh38.p7	10:21023260	TTTTAACCATTTTTT[-/A]AAACTGTAATTAGAA	10529
rs113896048	snp	A/C	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20970955	AGAAGTGAAAGTGGA[A/C]CCAATTGAATATTTC	10529
rs113903402	snp	C/G	0.00993419	0.0697739	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21136554	AAGAATCCTCAGAGT[C/G]AGCAAAAGCAGGAGA	10529
rs113913446	snp	A/G	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20787157	ACATGCTTGAGGGGA[A/G]ATGGGAAGACCAGCT	10529
rs113913461	in-del	-/GT	0.375	0.216506	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20852537	GTACCGTACGGGCAA[-/GT]GTGTACCTGACTTTG	10529
rs113918473	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21081538	GATATTTAACACACA[C/T]ATATAAACACATACA	10529
rs114008159	snp	A/T	0.00597247	0.0543191	intron-variant	NEBL	GRCh38.p7	10:20980785	TAACAAAAGTGAGAC[A/T]GATTTTCTTTGTAAG	10529
rs114010699	snp	G/T	0.0142736	0.0832652	intron-variant	NEBL	GRCh38.p7	10:20996375	CTGATCAATGTCACT[G/T]TATAGACAGCGAAGT	10529
rs114019613	snp	A/G	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21060194	AGTACAGCTGATTAA[A/G]CCTCTCAGTGTAAAG	10529
rs114021440	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21043346	TAGAAGCAGCCCTGT[C/T]AGAATTTTGAAAGCC	10529
rs114050789	snp	A/C	0.0193772	0.0965046	intron-variant	NEBL	GRCh38.p7	10:21170668	CCAAGAAAGTCCTGA[A/C]TTCTGTTCAATGCCC	10529
rs114053180	snp	A/T	0.0314385	0.121371	intron-variant	NEBL	GRCh38.p7	10:21012356	TGTGTATATATATAT[A/T]TATTTATTTATTTTA	10529
rs114071767	snp	A/G	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:20796999	CCTGATAAGAACTAC[A/G]TAATTCTGGGCAGTT	10529
rs114078330	snp	A/C	0.0182019	0.0936463	intron-variant	NEBL	GRCh38.p7	10:21158519	TAGGTGAGGAAACCG[A/C]GGGATGGTGAGGCAA	10529
rs114085205	snp	A/T	0.00156682	0.0279455	intron-variant	NEBL	GRCh38.p7	10:20835656	TTACAACATTCAAAC[A/T]CTCAGTGGGCAAACA	10529
rs114089295	snp	A/C	0.0275645	0.114116	intron-variant	NEBL	GRCh38.p7	10:20797977	GCATGGTGGAGGATG[A/C]CTGTCCTCCCAGTGA	10529
rs114095315	snp	A/G	0.0228947	0.104514	intron-variant	NEBL	GRCh38.p7	10:20989264	ACCTAGTTTAAAAAC[A/G]TATTTAATCCAACTT	10529
rs114097089	snp	C/G	0.0236746	0.106192	intron-variant, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20879992	CGTTTTGGCTTTAAA[C/G]TCAGCCATTAGGCAT	10529
rs114136458	snp	G/T	0.0142736	0.0832652	intron-variant	NEBL	GRCh38.p7	10:21165885	ACAGGTAACTTTCAG[G/T]GCTCTCTGATGTATG	10529
rs114138971	snp	C/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21054866	AATTTCATGAAACTT[C/G]AGAGTTAATTACCCA	10529
rs114144131	snp	C/T	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:21050373	AATTCTCACAGCCAA[C/T]GTGTAAAATCCCTAT	10529
rs114144708	snp	C/G	0.0372196	0.131242	intron-variant	NEBL	GRCh38.p7	10:21006695	TTTCCACAGTGGTCC[C/G]AGACCCGAAAAGCAT	10529
rs114167085	snp	C/T	0.0283406	0.115616	intron-variant	NEBL	GRCh38.p7	10:20802715	ACGAAATGAGTTGAT[C/T]GTTCAACCCTTTGTC	10529
rs114173989	snp	C/G	0.0372196	0.131242	intron-variant	NEBL	GRCh38.p7	10:20910615	GGTGGGCAGTGGAAA[C/G]CATGCAACACAGAAG	10529
rs114174978	snp	A/C	0.0221141	0.102801	intron-variant	NEBL	GRCh38.p7	10:20948568	ACAGGGGTGGACAAG[A/C]ACAAGTTTTGGAGAA	10529
rs114175770	snp	C/T	0.00993419	0.0697739	intron-variant	NEBL	GRCh38.p7	10:20975517	CAGTAGCAAGAGCTA[C/T]TATAGGGATTGTGTA	10529
rs114181489	snp	C/T	0.089084	0.191327	intron-variant	NEBL	GRCh38.p7	10:21049247	CATGGCCTAGCCAAG[C/T]TGACATATCACATTG	10529
rs114198157	snp	A/T	0.00557542	0.0525036	intron-variant	NEBL	GRCh38.p7	10:20904977	ATGAAAACACAGCAA[A/T]GTAAATAGTTTCCTA	10529
rs114214529	snp	C/T	0.00318978	0.0398085	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21135811	ATTTTCAGTGGTCAC[C/T]CTACTTTTCTTGGCT	10529
rs114257749	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20901743	ACTCATTTTTTGTTG[C/T]CTGGTTTTTGTTTTG	10529
rs114258352	snp	C/T	0.0263992	0.111815	intron-variant	NEBL	GRCh38.p7	10:20821099	CAAGCTTGAAAGAAA[C/T]CACTCTGGCTAAAGC	10529
rs114259521	snp	C/T	0.0158469	0.0875917	intron-variant	NEBL	GRCh38.p7	10:21072667	CTCAGTTGTTGGTCA[C/T]CTCTATTCAAGTGAC	10529
rs114264869	snp	A/G	0.00993419	0.0697739	intron-variant	NEBL	GRCh38.p7	10:20985752	TATTCAGGATGGAGA[A/G]TAGCTCTGTCTAAAA	10529
rs114272328	snp	A/G	0.0310518	0.120672	intron-variant	NEBL	GRCh38.p7	10:21153523	TATTAAAACAAATAT[A/G]TATATTATATATGTA	10529
rs114289069	snp	A/G	0.00597247	0.0543191	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20855379	ACATAGTCCATTACT[A/G]AGTTAAAATCCACAA	10529
rs114328008	snp	C/T	0.00755907	0.0610114	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21145506	CCTGACACTTAGGAA[C/T]CACTCGGTAAGTATC	10529
rs114331050	snp	A/C	0.00557542	0.0525036	intron-variant	NEBL	GRCh38.p7	10:20814257	TGACCTAAATCTATC[A/C]ACTCTAAACAAATGT	10529
rs114348887	snp	A/C	0.0166325	0.0896639	intron-variant	NEBL	GRCh38.p7	10:20914912	ACCCAGGCCGGAATG[A/C]AGTGGCACAATCTTG	10529
rs114355498	snp	C/T	0.00517822	0.0506191	intron-variant	NEBL	GRCh38.p7	10:20895532	TCGCAAGCTGCAATC[C/T]CTGGCACACAATAGT	10529
rs114373101	snp	C/T	0.0162398	0.0886349	intron-variant	NEBL	GRCh38.p7	10:20799080	GGTAAAATATAATCA[C/T]ATGATAGCCTACACA	10529
rs114378225	snp	C/T	0.0134861	0.0810011	intron-variant	NEBL	GRCh38.p7	10:21045842	AGAATTACTATGTAA[C/T]CCAGCAATCCCACTA	10529
rs114390265	snp	A/G	0.00517822	0.0506191	intron-variant	NEBL	GRCh38.p7	10:20902562	GCACAACAATTTCCA[A/G]GTTGGGTGTGGTGGG	10529
rs114397410	snp	C/G	0.0248432	0.108648	intron-variant	NEBL	GRCh38.p7	10:20791206	TAAGCATTTCAGGCT[C/G]TATATGGAATATTCT	10529
rs114400155	snp	A/G	0.0162398	0.0886349	upstream-variant-2KB	NEBL	GRCh38.p7	10:21176148	CCTGCGACCACAGGC[A/G]TATGCCACTATGCCC	10529
rs114401575	snp	C/T	0.00189573	0.030729	synonymous-codon, intron-variant	C10orf113, NEBL	GRCh38.p7	10:21146464	TTCAGAAATTTCAGG[C/T]GCCATGCTTTCCATA	10529
rs114404725	snp	C/T	0.0205511	0.0992634	intron-variant	NEBL	GRCh38.p7	10:21095864	CTGTTCAAAAGATGA[C/T]GGAACTAGAATGTAA	10529
rs114405399	snp	C/T	0.00795532	0.062565	intron-variant	NEBL	GRCh38.p7	10:21098352	TATGACTCTTTCCTC[C/T]TTGCAGCCCTACAAC	10529
rs114408160	snp	C/T	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:20834423	AAAATGGAACACTTA[C/T]TGATCAGGAAACCTA	10529
rs114444220	snp	C/T	0.0399052	0.1355	intron-variant	NEBL	GRCh38.p7	10:21102291	AATTGGCTCACAATA[C/T]AATGCATATATTTAG	10529
rs114448763	snp	C/T	0.0166325	0.0896639	intron-variant	NEBL	GRCh38.p7	10:21048717	TCTAAAGGTCTAGGC[C/T]GGGCACAGAGGCTCA	10529
rs114452742	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20794882	AGCCCTGCGCTTAGG[A/C]TGTCACATGCTTTAG	10529
rs114458077	snp	C/G	0.0271762	0.113356	intron-variant	NEBL	GRCh38.p7	10:21093596	ATATGCAACCAGATG[C/G]GGGTCACAGCATTTT	10529
rs114475775	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20876415	TTTTAATGCTAAATC[C/T]TAAAGCACTATTATT	10529
rs114479565	snp	A/C/T	0.0178257	0.0928375	intron-variant	NEBL	GRCh38.p7	10:20908966	ACTGATCACCAGACA[A/C/T]TGAGATCATAAAATT	10529
rs114487089	snp	C/T	0.0142736	0.0832652	intron-variant	NEBL	GRCh38.p7	10:20789265	GTAAAGTTTGAAAGA[C/T]TAAATATAAACATCT	10529
rs114492652	snp	A/C	0.0414363	0.137845	intron-variant	NEBL	GRCh38.p7	10:20955311	AAAGTGGAGAATATG[A/C]TGTGTGAAATGAGTG	10529
rs114505194	snp	A/G	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:21063197	TAACCCCATGCACAC[A/G]CAGTTCCGATCTTGC	10529
rs114517968	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20860677	GTAAGCTGTTTTGTT[C/T]TCTCATAATATTTTT	10529
rs114528683	snp	A/G	0.0134861	0.0810011	intron-variant	NEBL	GRCh38.p7	10:21039515	TGTCAGGTTTGTTGA[A/G]GATCAGATGGTTATA	10529
rs114534996	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21053328	CTATAATCCCACTTC[C/T]CACTCTTTTAAAATC	10529
rs114545555	snp	A/G	0.0185938	0.0946107	intron-variant	NEBL	GRCh38.p7	10:20935253	ACAACATGGGTATCA[A/G]TAACAAAGATCACAA	10529
rs114581286	snp	C/T	0.02016	0.0983543	intron-variant	NEBL	GRCh38.p7	10:21155786	GGTGCGTTGGAAAAG[C/T]ACTATCACATGGTCA	10529
rs114584294	snp	C/G	0.00597247	0.0543191	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20899493	AATGCACAAACTTTT[C/G]AAAACAAAAACCAAA	10529
rs114591546	snp	A/G	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:20912296	TATGTTTGAAATAAA[A/G]ATGCATTAGCTGGGT	10529
rs114594350	snp	C/G/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21167024	AGCAGCGAAATGGTA[C/G/T]GTGAGAGGCAGCGGA	10529
rs114596164	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21159289	AGCTAATGACTAGAC[C/T]AGTCACAGGGGTATG	10529
rs114617209	snp	A/C	0.0562307	0.157967	intron-variant	NEBL	GRCh38.p7	10:20972770	AATAAAAATTAAAAA[A/C]AAAATGTAAATGCAT	10529
rs114618279	snp	A/G	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:20893041	TTTACCCACAACAAC[A/G]TTCATTTGCCTGGAA	10529
rs114620380	snp	A/G	0.0023933	0.0345097	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20851495	GAACTTTGTGAAATG[A/G]CCGGGTGCAGTGGCT	10529
rs114662789	snp	C/T	0.0217236	0.101931	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20875083	CTTTGTTGCTTCCAA[C/T]GAATATTTGAATTCC	10529
rs114674192	snp	A/G	0.0205511	0.0992634	intron-variant	NEBL	GRCh38.p7	10:21149148	CCTATCCGGTGAAGC[A/G]TCCCAAAAAGGCCCA	10529
rs114674711	snp	G/T	0.0799831	0.183287	intron-variant	NEBL	GRCh38.p7	10:21027237	CCCAGCACAGGCCCC[G/T]TTGTGCGTAACAGGC	10529
rs114678832	snp	C/T	0.0744748	0.178019	intron-variant	NEBL	GRCh38.p7	10:21074393	CTAATATCATCCACT[C/T]CACAGAGGATGCTGT	10529
rs114690361	snp	C/G	0.0142736	0.0832652	intron-variant	NEBL	GRCh38.p7	10:21059294	ACCACTTGTGCTGGG[C/G]ACAGGCACTCTATCT	10529
rs114694270	snp	C/T	0.0325976	0.123435	intron-variant	NEBL	GRCh38.p7	10:20992270	CTTTTGAATGCCATT[C/T]CTAAGTTTCATCAAT	10529
rs114705621	snp	C/T	0.0115144	0.0749975	intron-variant	NEBL	GRCh38.p7	10:21148817	AGGTGTGAGCCACCA[C/T]GCCCGGCCCCTGTCC	10529
rs114714698	snp	A/G	0.00795532	0.062565	intron-variant	NEBL	GRCh38.p7	10:21078856	CTTGCTTATTAGCTG[A/G]CTGCCACTTGGTGGC	10529
rs114725202	snp	A/G	0.00795532	0.062565	intron-variant	NEBL	GRCh38.p7	10:20975697	GGTGGCAAAAGACTG[A/G]AAGCCTGCCTCCAAC	10529
rs114731102	snp	C/T	0.030665	0.119967	intron-variant	NEBL	GRCh38.p7	10:20987543	CCCAAACACTATATC[C/T]TCCACTCAGCTCTGC	10529
rs114742012	snp	A/C	0.0197687	0.0974348	intron-variant	NEBL	GRCh38.p7	10:20830464	TAAATTTTTGTGGTC[A/C]CTACTTCTCCCACAT	10529
rs114752859	snp	A/G	0.030278	0.119257	intron-variant	NEBL	GRCh38.p7	10:20905022	AAAGCTGTTTTTGTC[A/G]TGTTTCTAGGAGGAA	10529
rs114762423	snp	A/G	0.0130921	0.0798413	intron-variant	NEBL	GRCh38.p7	10:20977326	TGGCAGGTCGTCTTC[A/G]TTCCCCCATTTCTTA	10529
rs114774317	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21054483	GCTGTACTGCCTCTC[A/G]GACAGGCATCGGGGA	10529
rs114792331	snp	C/T	0.0185938	0.0946107	intron-variant	NEBL	GRCh38.p7	10:21017477	GATCTTTGGACATCT[C/T]GCCATTAGCTCTTGT	10529
rs114800560	snp	C/G	0.0134861	0.0810011	intron-variant	NEBL	GRCh38.p7	10:21166409	ATTCTGGTTACAACT[C/G]TCTAATGGGTAGCAG	10529
rs114803934	snp	G/T	0.00795532	0.062565	intron-variant	NEBL	GRCh38.p7	10:20914318	AGAGAACAAGAGCCA[G/T]AGAAACCTTAAAAGA	10529
rs114821984	snp	C/G	0.0142736	0.0832652	intron-variant	NEBL	GRCh38.p7	10:21002023	TAAGGTGATTTGTTA[C/G]TTAGTTGGGTTTTTC	10529
rs114824385	snp	A/G	0.0322114	0.122752	intron-variant	NEBL	GRCh38.p7	10:21014130	TTTTTTATTATTATT[A/G]ATATTATTTTAGATT	10529
rs114853097	snp	C/T	0.0314385	0.121371	intron-variant	NEBL	GRCh38.p7	10:21012203	AGTAGGGTAGGTGCC[C/T]CCCTTCAAGTGGGAC	10529
rs114865594	snp	A/T	0.0356815	0.128715	intron-variant	NEBL	GRCh38.p7	10:21032366	AAGGCATAATTATAA[A/T]GACTATAAGCCTGAT	10529
rs114866317	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21105119	TTGTTGAATTTTATT[A/G]GCTAAAAGTCTGTTA	10529
rs114869640	snp	A/T	0.0126979	0.078662	intron-variant	NEBL	GRCh38.p7	10:21163791	TGCACACATCGAACT[A/T]GTTCTCTTCTGGCTC	10529
rs114872087	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20839017	AGAGTGGTCTGGAAC[C/T]GAACCCATAGTATCT	10529
rs114874951	snp	C/T	0.0168055	0.0901129	intron-variant	NEBL	GRCh38.p7	10:21071671	CTGAACTGGGATCTC[C/T]AGGATTCATCCAGGA	10529
rs114875104	snp	A/G	0.000395498	0.0140568	intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20817668	AAATTGCAGTTCCCC[A/G]TTGAAGTTCTCCCTT	10529
rs114883079	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20913183	GTCATGATTAGAGCA[C/T]TGACTCAGCTTAGAG	10529
rs114886765	snp	C/T	0.00597247	0.0543191	intron-variant	NEBL	GRCh38.p7	10:20988881	TGAGCAGAGTTGAAC[C/T]GACCCTTCTTGAATG	10529
rs114890394	snp	A/C/T	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:20887577	GTGCATGCCAACAAA[A/C/T]GGCTAATTTTTGTAT	10529
rs114894183	snp	C/T	0.00676609	0.0577691	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20864031	ATTTTCATGGCAATT[C/T]ATAATGTGATTTTTA	10529
rs114899055	snp	C/T	0.00755907	0.0610114	intron-variant	NEBL	GRCh38.p7	10:20946665	CGAGGTTTCACCACG[C/T]TGTTGGCCAGGCTGG	10529
rs114904489	snp	A/G	0.0482946	0.147699	intron-variant	NEBL	GRCh38.p7	10:21076162	AACATAGAATTACCA[A/G]CCAGGCACGGTGGCT	10529
rs114918858	snp	A/G	0.00337613	0.0409471	intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20897195	ATATCCTCAAATACA[A/G]GGACCCTCATTTTTA	10529
rs114919253	snp	G/T	0.030278	0.119257	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21133145	GTTAATTTTGTATGT[G/T]TGTGAGGTGGGAGTC	10529
rs114922796	snp	C/T	0.00557542	0.0525036	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20860990	ATAATAAAAAATTTC[C/T]GATATTCTCAATACC	10529
rs114937558	snp	C/T	0.0154538	0.0865337	intron-variant, downstream-variant-500B	NEBL	GRCh38.p7	10:20815271	GCATTTAACAATCCA[C/T]GTTCAATGAAATATT	10529
rs114946953	snp	C/T	0.0248432	0.108648	intron-variant	NEBL	GRCh38.p7	10:20927291	CTTTAAAATTTATAT[C/T]AACTTTAAATTATTC	10529
rs114953165	snp	C/T	0.0130921	0.0798413	intron-variant	NEBL	GRCh38.p7	10:20978836	AAAGTTGGAGCCACT[C/T]GAGAGCAAGAGGAGT	10529
rs114965148	snp	A/C	0.0379877	0.132479	intron-variant	NEBL	GRCh38.p7	10:21114892	GTTTAGACCATTTAC[A/C]TTTAATGTGGCTATT	10529
rs114965393	snp	C/T	0.0185938	0.0946107	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21136247	CCAATTCTCTAGTAA[C/T]ATATTTCCAAAATCT	10529
rs114966199	snp	C/G/T	0.0123103	0.0775472	intron-variant	NEBL	GRCh38.p7	10:20837642	TTGATGCAGACAAAC[C/G/T]AGCCTTCTATTGGAA	10529
rs114985052	snp	A/G	0.00636936	0.0560724	intron-variant	NEBL	GRCh38.p7	10:20810975	AAGGTTACACAGCTC[A/G]TAAGAAGTAGCAGAG	10529
rs114999839	snp	A/G	0.0158469	0.0875917	intron-variant	NEBL	GRCh38.p7	10:21049143	AAAGTGATCCGTACT[A/G]AAAGTGTACTGATTA	10529
rs115008697	snp	A/C	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21021439	GCCAGGCCTCTGCAG[A/C]CTTCTCACTGTGAAA	10529
rs115034474	snp	C/G	0.00557542	0.0525036	intron-variant	NEBL	GRCh38.p7	10:20807653	CCAAGGTGTTAAGTT[C/G]CTCAACCTCAAAATT	10529
rs115042607	snp	A/G	0.00478085	0.0486577	intron-variant	NEBL	GRCh38.p7	10:21086864	TACCAGTTTGCTGAA[A/G]AGTTCAGTCATGTCT	10529
rs115042784	snp	A/T	0.0193772	0.0965046	intron-variant	NEBL	GRCh38.p7	10:21102453	ACCCAAACCCAGGGA[A/T]CCAACAATATGCTTT	10529
rs115082239	snp	A/C/G	0.0174548	0.0920773	intron-variant	NEBL	GRCh38.p7	10:20806586	CCCTCATTCCACCCC[A/C/G]TCACAGGCCTGATTC	10529
rs115122175	snp	G/T	0.0209421	0.100162	intron-variant	NEBL	GRCh38.p7	10:21110794	TTATCTTTAAGAACA[G/T]TCAGGTTAGGGACTC	10529
rs115123140	snp	C/G	0.0360663	0.129354	intron-variant	NEBL	GRCh38.p7	10:20887025	CTCACGTAGCTGAGA[C/G]AGCTAAAGAATAGAT	10529
rs115163736	snp	A/C	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:20791957	TACCATTCCCACTTT[A/C]CAGAACAAAATACAA	10529
rs115191718	snp	A/C	0.0452528	0.143452	intron-variant	NEBL	GRCh38.p7	10:20937759	TACAGCACTTTTCCG[A/C]CGGTTTTAGCAAACG	10529
rs115202568	snp	G/T	0.0130921	0.0798413	intron-variant	NEBL	GRCh38.p7	10:20989051	TGAATTTACAGTAAA[G/T]GTCAAAACCATGATT	10529
rs115210407	snp	C/T	0.0182019	0.0936463	intron-variant	NEBL	GRCh38.p7	10:20832225	TAAATCATTATACCC[C/T]ATCACCCACACTGCA	10529
rs115223938	snp	C/G	0.00636936	0.0560724	intron-variant	NEBL	GRCh38.p7	10:20904864	GAGCCAGAAAGAGAG[C/G]AGGCTTGATCACTCT	10529
rs115235780	snp	A/T	0.00795532	0.062565	intron-variant	NEBL	GRCh38.p7	10:20907837	AGCCAGCACAATTGG[A/T]ACTTTAAAACTGCTG	10529
rs115252545	snp	C/G	0.00953873	0.0683987	intron-variant	NEBL	GRCh38.p7	10:21100934	AGTTTTTGTTTCTTT[C/G]TTTGTTTTAATCGAA	10529
rs115254514	snp	C/T	0.0197687	0.0974348	intron-variant	NEBL	GRCh38.p7	10:21085419	TTGAAGCCAGGAGTT[C/T]GAGACCAGTCTGGGC	10529
rs115256029	snp	A/G	0.00557542	0.0525036	intron-variant	NEBL	GRCh38.p7	10:20904973	TTTTATGAAAACACA[A/G]CAATGTAAATAGTTT	10529
rs115261348	snp	A/G	0.0174175	0.0916809	intron-variant	NEBL	GRCh38.p7	10:21027933	TATCTTTAAAGAATG[A/G]GAAATAGGCCAAGTG	10529
rs115277987	snp	C/T	0.0111196	0.0737302	intron-variant	NEBL	GRCh38.p7	10:21038200	CATGCACTCCCTCCA[C/T]ATATTTTTTTTATTT	10529
rs115300837	snp	A/G	0.0103295	0.0711199	intron-variant	NEBL	GRCh38.p7	10:21076067	TGTGGAGAAATTGGA[A/G]CTTTTATGCATTATC	10529
rs115301870	snp	A/T	0.0456336	0.143994	intron-variant	NEBL	GRCh38.p7	10:21150596	AAATATAAAAATGAG[A/T]TGTGAAAACTTCAGA	10529
rs115302239	snp	C/T	0.0205511	0.0992634	intron-variant	NEBL	GRCh38.p7	10:21104601	TTCTCACTAAACTCA[C/T]GTATTAGTTCAGTTG	10529
rs115313923	snp	A/T	0.00478085	0.0486577	intron-variant	NEBL	GRCh38.p7	10:20947352	CATCCTCATATCCTC[A/T]TTGGCTAGAACAGCA	10529
rs115321210	snp	A/T	0.00835141	0.0640778	intron-variant	NEBL	GRCh38.p7	10:21096719	GAAGTCTCACTATGT[A/T]GCCCAAGCTAGTCTC	10529
rs115350637	snp	C/T	0.0763149	0.179815	intron-variant	NEBL	GRCh38.p7	10:21095346	AGATAAAAGATAAGA[C/T]GAACATGGTCAGAGT	10529
rs115369018	snp	C/T	0.0115144	0.0749975	intron-variant	NEBL	GRCh38.p7	10:21115489	AAGGTCTTTATTTCA[C/T]CTATTCTTTAATTTT	10529
rs115378097	snp	C/T	0.0463947	0.145069	intron-variant	NEBL	GRCh38.p7	10:20974685	AACCTTTAATGGTTA[C/T]ACATACTACCAATTA	10529
rs115378522	snp	A/G	0.0174175	0.0916809	intron-variant	NEBL	GRCh38.p7	10:20922686	AGAGTCAAGGAGGCC[A/G]TCCAGAATGCAGCCC	10529
rs115379925	snp	A/G	0.00517822	0.0506191	intron-variant	NEBL	GRCh38.p7	10:20977436	CAAATTTCTAGTTAT[A/G]GTACAAATAGAGGTA	10529
rs115384039	snp	A/G	0.00953873	0.0683987	intron-variant	NEBL	GRCh38.p7	10:20988704	CTCAAATAGTTATCC[A/G]GATTCACAGCTTTGA	10529
rs115384345	snp	C/G	0.0142736	0.0832652	intron-variant	NEBL	GRCh38.p7	10:21002617	AAGCATGGATGGAGA[C/G]GTCTCAGGAAACTCA	10529
rs115385706	snp	A/G	0.00438332	0.0466095	intron-variant	NEBL	GRCh38.p7	10:20913829	CAATCATATATATGA[A/G]ACAATGAATATTTAT	10529
rs115395832	snp	A/G	0.00914312	0.0669923	intron-variant	NEBL	GRCh38.p7	10:20955428	GGATCAGGGGGCTGG[A/G]CTGTCATTTACAGAT	10529
rs115400216	snp	C/T	0.00953873	0.0683987	intron-variant	NEBL	GRCh38.p7	10:21118484	CACAGTATGTAACTC[C/T]GAGCTTTTCTCTACT	10529
rs115404852	snp	A/G	0.029116	0.117091	intron-variant	NEBL	GRCh38.p7	10:20913226	GTTCAGACAGCCACA[A/G]GCAATTCCTAGAGTA	10529
rs115434180	snp	C/T	0.0217236	0.101931	intron-variant	NEBL	GRCh38.p7	10:20995035	AAAAATGCTTACAAA[C/T]ACCTCTCCCAAAAGC	10529
rs115434294	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21063402	ATAGTCACGAGATGC[C/T]TACTATTTGAGACTC	10529
rs115434655	snp	C/T	0.0119091	0.0762411	intron-variant	NEBL	GRCh38.p7	10:21095490	ACGGTGCTATTAGCA[C/T]AACTGTACCTTTTAA	10529
rs115449554	snp	A/G	0.00199481	0.0315187	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20884381	AGCATCTGGCCAAAT[A/G]TGGCATTGAAATTGG	10529
rs115469238	snp	C/T	0.030665	0.119967	intron-variant	NEBL	GRCh38.p7	10:20985343	AATGGATCACAGCAA[C/T]TCTAACCTCATAGGC	10529
rs115499380	snp	C/T	0.00676609	0.0577691	intron-variant	NEBL	GRCh38.p7	10:20832791	TGGAGTATTTTGCCT[C/T]CTATCTTCCACTCAT	10529
rs115511905	snp	C/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20799354	AGATACCAGGTCTCA[C/T]CATGTTGGCCAAGCT	10529
rs115515592	snp	A/T	0.0150606	0.0854603	intron-variant	NEBL	GRCh38.p7	10:21064494	TAACTCAACCTTCAG[A/T]AAAAATGAGCAATAT	10529
rs115518885	snp	C/G	0.00159617	0.0282053	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20876079	GCTGTGCATAAAAAC[C/G]TACTAAATTATTAAA	10529
rs115523390	snp	C/T	0.0115144	0.0749975	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20881165	TCATCTAGCTTAAAC[C/T]TCGGGTGTAGTTTTG	10529
rs115528595	snp	A/G	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:21040980	GCATGTGGAACCAAG[A/G]GCCAATTAAGCCCAT	10529
rs115550513	snp	A/G	0.0517044	0.152246	intron-variant	NEBL	GRCh38.p7	10:20978443	ACCAAAAAAAAAAAC[A/G]AGTTATTTGATTAAA	10529
rs115555704	snp	A/G	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:21032901	ATAAAAGAAGGCATT[A/G]TCAAAGGGATTATAC	10529
rs115597111	snp	C/T	0.0267878	0.112589	intron-variant	NEBL	GRCh38.p7	10:21014253	CTCAGCCTTCCAAAA[C/T]ACTGGGATTACAGGA	10529
rs115600826	snp	C/T	0.0818113	0.184966	intron-variant	NEBL	GRCh38.p7	10:21089426	CTGGGACACGCAGCA[C/T]GGAGGATTTCCATCA	10529
rs115611932	snp	A/C	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:20893044	ACCCACAACAACGTT[A/C]ATTTGCCTGGAAAAT	10529
rs115628926	snp	C/T	0.0322114	0.122752	intron-variant	NEBL	GRCh38.p7	10:21015994	AAAGCCTGATGCCCC[C/T]GCAGGTGAACTATAA	10529
rs115630327	snp	A/C	0.00755907	0.0610114	intron-variant	NEBL	GRCh38.p7	10:20824949	ATACTTCTCTCCCAA[A/C]CTAATTCATCTACCA	10529
rs115639800	snp	G/T	0.0182019	0.0936463	intron-variant	NEBL	GRCh38.p7	10:21008735	CCTGTGCCTAATTTA[G/T]AAATTAAGCTTTATT	10529
rs115640992	snp	C/G	0.0310518	0.120672	intron-variant	NEBL	GRCh38.p7	10:21012156	TCCGATTTTCTGCTT[C/G]CTTCGTACAATCTAC	10529
rs115663559	snp	C/T	0.00953873	0.0683987	intron-variant	NEBL	GRCh38.p7	10:21077059	GTAACCTTTATGTTA[C/T]GTATATCTTACCACA	10529
rs115687256	snp	A/T	0.0217236	0.101931	intron-variant	NEBL	GRCh38.p7	10:20919890	AAAACCACCACTGCA[A/T]GCAAAAGCAAGGTAG	10529
rs115693223	snp	C/T	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:20839762	TGCCAGGTGTAAGCA[C/T]AGGATAGAGATTAAT	10529
rs115699899	snp	A/G	0.00795532	0.062565	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20847660	GGGGAGGAAACTAGA[A/G]GGAGGTCCAGCCTGA	10529
rs115707814	snp	C/T	0.0130921	0.0798413	intron-variant	NEBL	GRCh38.p7	10:21102822	CATGTTTTTTGTTTG[C/T]TTGTTTTATTTTTAT	10529
rs115708584	snp	A/G	0.00438937	0.0466414	synonymous-codon, upstream-variant-2KB	NEBL	GRCh38.p7	10:20961672	TAAACAGGCACCTAC[A/G]TTACTGATTTGCTCC	10529
rs115728323	snp	A/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21162344	TGTTCCAGCTAATTA[A/T]CAAATCTGAGGGGGT	10529
rs115745376	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21056565	AGAAATGTTGAACAT[A/G]CATAGAGAACGAGCC	10529
rs115745902	snp	A/G	0.00438332	0.0466095	intron-variant	NEBL	GRCh38.p7	10:20841154	AGATCTTAAGAACAC[A/G]TGTTCCTTATTAATT	10529
rs115751438	snp	G/T	0.00636936	0.0560724	intron-variant	NEBL	GRCh38.p7	10:20828688	TGTGTGCGCACATGT[G/T]AGAGGGAGGGAGGGA	10529
rs115795896	snp	C/T	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:20831669	TTTTGACATTAAGAC[C/T]ATGTCTTTTGGAATG	10529
rs115800000	snp	C/T	0.00953873	0.0683987	intron-variant	NEBL	GRCh38.p7	10:21118785	TTAAGTTTCTCTTTC[C/T]TATGAATGCATAGTC	10529
rs115800293	snp	C/T	0.00438332	0.0466095	intron-variant	NEBL	GRCh38.p7	10:20793534	AATTGCATAATGGTG[C/T]CTTATTTTTCTTTCT	10529
rs115802060	snp	A/T	0.00676609	0.0577691	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20875276	TCGTGCAGAGCATCC[A/T]AGGTGCCCGGCTATC	10529
rs115804934	snp	A/G	0.0158469	0.0875917	intron-variant	NEBL	GRCh38.p7	10:20836220	CTGTTATGGTGCTTT[A/G]TGATCAGTGATTTTT	10529
rs115809731	snp	A/T	0.0232847	0.105357	intron-variant	NEBL	GRCh38.p7	10:21068651	TTTTCAGCTGTCAGC[A/T]ACTAAGCCAGTACAC	10529
rs115828476	snp	C/T	0.00914312	0.0669923	intron-variant	NEBL	GRCh38.p7	10:20976871	GCCAAACCTCAGCAT[C/T]ACACAATATACCCAT	10529
rs115833259	snp	A/G	0.031825	0.122064	intron-variant	NEBL	GRCh38.p7	10:21005054	GGTTCTTACTGGCCT[A/G]AGAGTAACACCTTAT	10529
rs115834109	snp	C/T	0.0333695	0.124785	intron-variant	NEBL	GRCh38.p7	10:21010383	CTGAGTAGGTGGGAC[C/T]ACAGGTGTGTGCTAC	10529
rs115838974	snp	C/T	0.00597247	0.0543191	intron-variant	NEBL	GRCh38.p7	10:21027677	TGTGACTTCACATCA[C/T]GAAACTGGCTTTTTA	10529
rs115867736	snp	A/G	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:20798306	GCACGTGGAAATATT[A/G]AAGAGTTCCTCTAAA	10529
rs115872320	snp	C/G	0.0182019	0.0936463	intron-variant	NEBL	GRCh38.p7	10:21154222	CCAGCACTTTGGAAG[C/G]CCGAAGCAGGAAGAT	10529
rs115873743	snp	C/T	0.00993419	0.0697739	intron-variant	NEBL	GRCh38.p7	10:21104442	CCAGTGTAGAAGTTT[C/T]ACACATTTTTCCTCA	10529
rs115908077	snp	C/T	0.0107246	0.0724382	intron-variant	NEBL	GRCh38.p7	10:21085483	ACAAACAAAAAAACT[C/T]AATTAGCCAAGCATA	10529
rs115912857	snp	C/T	0.00993419	0.0697739	intron-variant	NEBL	GRCh38.p7	10:21088098	CATGCTACATGTCCA[C/T]CAGGAATCACCCCTG	10529
rs115914225	snp	C/T	0.0279526	0.114869	intron-variant	NEBL	GRCh38.p7	10:21068006	TAATATACTTCCCTA[C/T]GAAGTAATAAATACA	10529
rs115922291	snp	C/T	0.0252325	0.109451	intron-variant	NEBL	GRCh38.p7	10:20787604	AAATTTTTCATACTC[C/T]CTTAATGAAATCATG	10529
rs115936686	snp	C/T	0.0314385	0.121371	intron-variant	NEBL	GRCh38.p7	10:21000719	AGCAACACCCCAAAA[C/T]GACAAAGTGAGCAAA	10529
rs115959829	snp	C/T	0.0130921	0.0798413	intron-variant	NEBL	GRCh38.p7	10:20994726	GCTCTATATTATATA[C/T]TGTGTTCTTACAATA	10529
rs115976061	snp	A/T	0.00716266	0.059414	intron-variant	NEBL	GRCh38.p7	10:20795524	AGTCATTTTAGCATC[A/T]GACAAGTCTCTGGGG	10529
rs115977793	snp	A/G	0.00993419	0.0697739	intron-variant	NEBL	GRCh38.p7	10:21048072	CAATGCAAAGTGAGC[A/G]GTTCTCCAAGACAAA	10529
rs116007437	snp	C/T	0.0217236	0.101931	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20871508	AACAGGCTCCCTGTG[C/T]GTTATGTTATTTTAT	10529
rs116015764	snp	A/G	0.00318978	0.0398085	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21139538	AAAGAAATTATATGA[A/G]GTTTAGCCTCATGTT	10529
rs116054193	snp	A/C	0.0182019	0.0936463	intron-variant	NEBL	GRCh38.p7	10:20833354	AGATCCATTGACTTT[A/C]TTTGAAAAATAAACT	10529
rs116058144	snp	A/G	0.031825	0.122064	intron-variant	NEBL	GRCh38.p7	10:21025624	GGAATGAGAAAGAAC[A/G]TGACTGGGGAGAGCG	10529
rs116116554	snp	C/T	0.0146672	0.084371	intron-variant	NEBL	GRCh38.p7	10:20998598	ACCATAAAAATGCTA[C/T]GTCTACATCTCATAC	10529
rs116122805	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21056154	TTATCTGCTTTTAAC[A/G]GTAGAGAATATTTTG	10529
rs116138360	snp	C/T	0.031825	0.122064	intron-variant	NEBL	GRCh38.p7	10:21005064	GGCCTGAGAGTAACA[C/T]CTTATGCCCTCCATT	10529
rs116154181	snp	A/G	0.00716266	0.059414	intron-variant	NEBL	GRCh38.p7	10:20802178	AGAAAACTGCAAGTT[A/G]AGGAAAACCAAAGAA	10529
rs116157103	snp	A/G	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:21152466	CCTCAGCATAAATCC[A/G]CAGGACACTGAAGTG	10529
rs116158048	snp	A/T	0.039522	0.134904	intron-variant	NEBL	GRCh38.p7	10:21102901	GGTAAGAGTGTGCCA[A/T]AGCGGTTTGCTGTAC	10529
rs116176285	snp	A/C/T	0.0142791	0.083329	intron-variant	NEBL	GRCh38.p7	10:21056757	AAAAGCAAAATACTG[A/C/T]GAGAAAGAAAGCAAA	10529
rs116177506	snp	A/G	0.00557542	0.0525036	intron-variant	NEBL	GRCh38.p7	10:20826730	TTGGTTTTATATCCC[A/G]TAATCTCACAAATAA	10529
rs116177707	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21054039	CTCCATCTCAAAACA[A/C]AAAACAAAAAACAAA	10529
rs116178411	snp	A/C/G	0.0322114	0.122752	intron-variant	NEBL	GRCh38.p7	10:21022645	TTCTTAGAGTATAAA[A/C/G]GAATCTAGTTATATT	10529
rs116187316	snp	C/T	0.0170251	0.090679	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20961993	TTTAAGCAAGTTCTT[C/T]AACCACTCTGTGCTC	10529
rs116188549	snp	A/G	0.0142736	0.0832652	intron-variant	NEBL	GRCh38.p7	10:20996685	GCTAGACTGTAATGT[A/G]AAGCTATTAAACTGC	10529
rs116190320	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21057501	TTCAAATCTGAAATT[A/C]TGTTAAGAATCTAAA	10529
rs116195514	snp	A/G	0.0119091	0.0762411	intron-variant	NEBL	GRCh38.p7	10:21012185	ACCATGGCCAGAAGT[A/G]GGAGTAGGGTAGGTG	10529
rs116208556	snp	A/G	0.0295035	0.117819	intron-variant	NEBL	GRCh38.p7	10:21123046	TTTTTGAAATATCTC[A/G]TATCAGTGGGATTTC	10529
rs116209989	snp	C/T	0.00953873	0.0683987	intron-variant	NEBL	GRCh38.p7	10:21117852	GTTCAAGTAGCAACT[C/T]GGCCGCTATTATCTC	10529
rs116212108	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21044599	AAATTCACATGGCTG[C/T]TCACAGATTCTTCCC	10529
rs116223992	snp	A/C	0.00953873	0.0683987	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20863747	TCTCCATGGAGCCTG[A/C]CTTGTGGGAAGTGAA	10529
rs116242601	snp	A/C	0.0134861	0.0810011	intron-variant	NEBL	GRCh38.p7	10:21155204	ACTCCCTCACACACA[A/C]AAAAAAATTTTTTAG	10529
rs116244125	snp	A/T	0.0197687	0.0974348	intron-variant	NEBL	GRCh38.p7	10:21100474	TGCACCCTGTGTAAA[A/T]GATAAAGAGTGCAAA	10529
rs116245017	snp	C/T	0.0138799	0.0821421	intron-variant	NEBL	GRCh38.p7	10:21069178	ACAGTCATGAGCCAC[C/T]ACACCTGGCCCATCA	10529
rs116248841	snp	C/G	0.0325976	0.123435	intron-variant	NEBL	GRCh38.p7	10:20809247	GTCAAATCAAGCCAT[C/G]ATTCGTACCCCAACT	10529
rs116282032	snp	A/G	0.0217236	0.101931	intron-variant	NEBL	GRCh38.p7	10:20832138	CTCTGATTTGCCACT[A/G]GACAAGTCAATGTTC	10529
rs116289363	snp	A/C	0.0310518	0.120672	intron-variant	NEBL	GRCh38.p7	10:21013197	GAAGGAAATGTACCA[A/C]ATCCAGTGAATTCAT	10529
rs116312027	snp	A/T	0.0154538	0.0865337	intron-variant	NEBL	GRCh38.p7	10:20822573	AAGACTATATAGAGA[A/T]ATATACAGACTATCT	10529
rs116348608	snp	C/T	0.00874735	0.0655527	intron-variant	NEBL	GRCh38.p7	10:20919787	ACTCAAAATCCGGAA[C/T]CTACAGGAAAAATAA	10529
rs116349488	snp	C/T	0.0425829	0.139564	intron-variant	NEBL	GRCh38.p7	10:21157240	AACACTGATCTTTTA[C/T]AAGCTTTATTGAGGT	10529
rs116351021	snp	C/G	0.0205511	0.0992634	intron-variant	NEBL	GRCh38.p7	10:21108895	CTTGGTGAATCGATC[C/G]CTTTACCAACAATGG	10529
rs116367088	snp	C/T	0.0182019	0.0936463	intron-variant	NEBL	GRCh38.p7	10:21093976	TTTTCCATTCTAAGC[C/T]TTCCATAGAAAACTA	10529
rs116367943	snp	A/C	0.0205511	0.0992634	intron-variant	NEBL	GRCh38.p7	10:21060025	CTTTGGGTTCTGCCA[A/C]ATACAAATATTTTAA	10529
rs116371193	snp	A/G	0.030665	0.119967	intron-variant	NEBL	GRCh38.p7	10:20974075	AATATGAGAAACTGA[A/G]GCTTAGTGGTTTAGT	10529
rs116378787	snp	G/T	0.0486741	0.148216	intron-variant	NEBL	GRCh38.p7	10:20907291	TAAGGGTTTAAATTT[G/T]TATTATAAATAATGA	10529
rs116395454	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20801792	GAGTTCCAGAATGTA[C/T]TGAAGCATCTCTTGC	10529
rs116402585	snp	A/G	0.0923359	0.194016	intron-variant	NEBL	GRCh38.p7	10:21055085	ACCATAGTTCATTAT[A/G]TCTGGGGGAGTTGTT	10529
rs116403433	snp	A/C/G	0.088204	0.19271	intron-variant	NEBL	GRCh38.p7	10:21050547	ATGTCACTGCAGTAC[A/C/G]GGGAGAAGCATGAGA	10529
rs116409309	snp	C/T	0.0333695	0.124785	intron-variant	NEBL	GRCh38.p7	10:21016304	AGAGCTAACTCTTGG[C/T]TTGTTTGTTTATTCA	10529
rs116429640	snp	C/T	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21142839	CCTGAAGATCTGAGG[C/T]GGGACAGTGTCATCC	10529
rs116433893	snp	A/T	0.0232847	0.105357	intron-variant	NEBL	GRCh38.p7	10:20902475	AGATGTAGATCCCAC[A/T]CACAAATGAGAGCTA	10529
rs116466623	snp	G/T	0.0217236	0.101931	intron-variant	NEBL	GRCh38.p7	10:20886201	AATTTTTTTTAATAA[G/T]ATTATCTAGGTATCT	10529
rs116466943	snp	C/T	0.0126979	0.078662	intron-variant	NEBL	GRCh38.p7	10:20803224	TATAGTTAGCAAGAA[C/T]ATATTATACAGTTTC	10529
rs116468869	snp	A/G	0.00874735	0.0655527	intron-variant	NEBL	GRCh38.p7	10:20910875	GTAACCTATGCTAAA[A/G]AGTAGGCACTGGCCA	10529
rs116524169	snp	A/G	0.0205511	0.0992634	intron-variant	NEBL	GRCh38.p7	10:20905585	ATACGGATTACAATT[A/G]GAGCTGAGATTTGGG	10529
rs116535576	snp	C/T	0.0263992	0.111815	intron-variant	NEBL	GRCh38.p7	10:21001402	TTCCTATCAGAAAGA[C/T]TTTTCCAACTTGTAA	10529
rs116551035	snp	C/T	0.00557542	0.0525036	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20859391	ATAGCCATAATTACA[C/T]GAGGTAACTACTGTC	10529
rs116556909	snp	A/G	0.00953873	0.0683987	intron-variant	NEBL	GRCh38.p7	10:21101393	ACAATCCACGCAGAA[A/G]TGATGGGTAGAAATT	10529
rs116559922	snp	C/T	0.0138799	0.0821421	intron-variant	NEBL	GRCh38.p7	10:21064292	CACAGATTTGTTCAC[C/T]TCTTTGAAAACTTTT	10529
rs116588125	snp	A/G	0.00676609	0.0577691	intron-variant	NEBL	GRCh38.p7	10:20889732	GTAGCTATTACTAAC[A/G]TTCAGTAGTGCTTTT	10529
rs116589164	snp	A/C	0.0322114	0.122752	intron-variant, utr-variant-5-prime	NEBL	GRCh38.p7	10:20958155	GCCCAGTAGCAGCCA[A/C]AGAAAAGGGTGTTTC	10529
rs116592455	snp	A/G	0.0189856	0.0955633	intron-variant	NEBL	GRCh38.p7	10:20999319	AATACAAGCCAGGCT[A/G]GATGCAGTGGCTCAC	10529
rs116593439	snp	A/C	0.093777	0.195178	intron-variant	NEBL	GRCh38.p7	10:21056825	AAGCAAGGAAATTAT[A/C]ACCACAAAATTCAGG	10529
rs116597023	snp	A/G	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20953317	CATGCACACACCAAC[A/G]AAAGGCCACATGAGG	10529
rs116608031	snp	C/T	0.0130921	0.0798413	intron-variant	NEBL	GRCh38.p7	10:21121159	TAAAATTATACTCTT[C/T]CATTCCTTATCTCAA	10529
rs116609183	snp	C/T	0.0325976	0.123435	intron-variant	NEBL	GRCh38.p7	10:21115942	TCCGTTAATTCTTTT[C/T]AGTCTTCTTTTTTCA	10529
rs116612983	snp	A/G	0.00636936	0.0560724	intron-variant	NEBL	GRCh38.p7	10:20834794	CTTTTATATTCTCAG[A/G]TTTTCTGGGGAAGTT	10529
rs116619494	snp	A/G	0.00557542	0.0525036	intron-variant	NEBL	GRCh38.p7	10:20824015	ACATATATTTAGAGG[A/G]AGATCAATCAGGCAA	10529
rs116647769	snp	A/G	0.00795532	0.062565	intron-variant	NEBL	GRCh38.p7	10:21071777	GTTCCAAAGATCAGA[A/G]GTCCAAAATCAAAGT	10529
rs116675054	snp	C/T	0.067446	0.170804	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20853415	AGCAACCTAAGTGTC[C/T]ATCAACAGATGAATG	10529
rs116683576	snp	C/T	0.0364509	0.129988	intron-variant	NEBL	GRCh38.p7	10:20972127	ACTAGCTTAAAGAAA[C/T]AGGATAAACCCAGAA	10529
rs116684157	snp	A/G	0.0142736	0.0832652	intron-variant	NEBL	GRCh38.p7	10:20997242	AATGGTGGGGTTGCA[A/G]AGATAATGGGATCAG	10529
rs116689826	snp	C/T	0.0134861	0.0810011	intron-variant	NEBL	GRCh38.p7	10:20954639	GCAAGGCCAGAGTCC[C/T]CTGCTAGAGAGCTTC	10529
rs116714054	snp	A/C	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:21088939	AGTTAATGAACCACG[A/C]GAGGCAGGAAAGATT	10529
rs116730101	snp	A/T	0.00517822	0.0506191	intron-variant	NEBL	GRCh38.p7	10:21079834	ATTTGTTCTTTGTAC[A/T]CTGCCCCACCACCCA	10529
rs116731874	snp	A/G	0.0372196	0.131242	intron-variant	NEBL	GRCh38.p7	10:21103725	CAAATATTTTCTCCT[A/G]TTCTCTGGCTCCCTA	10529
rs116780903	snp	G/T	0.0221141	0.102801	intron-variant	NEBL	GRCh38.p7	10:20909831	TACAATGGCTTTAAG[G/T]CTTAAATTAAGGAAC	10529
rs116782704	snp	C/T	0.0486741	0.148216	intron-variant	NEBL	GRCh38.p7	10:20957245	TAAATCAGCAGTATC[C/T]GTGTGAGCTTATTAA	10529
rs116798162	snp	A/C/G	0.0174175	0.0916809	intron-variant	NEBL	GRCh38.p7	10:21164343	GTGTCATGCATGGCT[A/C/G]TGTCTGTATCTCTCT	10529
rs116831926	snp	A/G	0.0364509	0.129988	intron-variant	NEBL	GRCh38.p7	10:20900388	GAAGTTAATAAAAAG[A/G]AAGCACTGGCTGGGT	10529
rs116837617	snp	A/G	0.0517044	0.152246	intron-variant	NEBL	GRCh38.p7	10:21115499	TTTCATCTATTCTTT[A/G]ATTTTTTTTTCACTT	10529
rs116838703	snp	C/T	0.0368353	0.130617	intron-variant	NEBL	GRCh38.p7	10:21076072	AGAAATTGGAACTTT[C/T]ATGCATTATCAGCGG	10529
rs116839937	snp	A/C	0.0547245	0.156101	intron-variant	NEBL	GRCh38.p7	10:21009030	TTCTAGAATAAAAAG[A/C]TTCAAAGCCTTGGAA	10529
rs116864244	snp	A/G	0.0275645	0.114116	intron-variant	NEBL	GRCh38.p7	10:20792076	GTGAAGGTTTTGAAG[A/G]CCCCTCAATGACTAT	10529
rs116887975	snp	A/T	0.0111196	0.0737302	intron-variant	NEBL	GRCh38.p7	10:20989792	TACAGGAGTAAATCT[A/T]TTGGAGCAGGGGTCC	10529
rs116894706	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21105025	TATGGAAAACATTGA[C/T]TGATCTTTTTTAAGG	10529
rs116937144	snp	A/C	0.0471551	0.14613	intron-variant	NEBL	GRCh38.p7	10:21058099	TCAGAAATGATACTA[A/C]TAACAGCTACTATCA	10529
rs116956181	snp	A/G	0.11228	0.208646	intron-variant	NEBL	GRCh38.p7	10:20929780	GGGATGACAGATGAA[A/G]AGTTACGAAATGAGT	10529
rs116960318	snp	C/G	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:20944915	AGAGGCCACAAGATC[C/G]CATATGACAATTAGA	10529
rs116972894	snp	A/G	0.221141	0.248329	intron-variant	NEBL	GRCh38.p7	10:21081047	TTTAGTACAAACAGT[A/G]TTTCACCATGTTGGC	10529
rs116973001	snp	G/T	0.000798403	0.0199641	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20861149	TTTATACAGTAGGTG[G/T]CACAAAAGCAATGAT	10529
rs116981297	snp	A/G	0.0193772	0.0965046	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21136863	CATAACTTCTTACTC[A/G]TCTCTGGATGGAGGA	10529
rs116983900	snp	A/G	0.00159617	0.0282053	intron-variant, downstream-variant-500B	NEBL	GRCh38.p7	10:20817108	AAGTCACCCAGGCCC[A/G]GTGGCACACATCTGT	10529
rs116985638	snp	A/G	0.0189856	0.0955633	intron-variant	NEBL	GRCh38.p7	10:20787943	TCAGCTAAATACGTT[A/G]CAAAAGCCTGAGAAA	10529
rs117000172	snp	A/G	0.0463947	0.145069	intron-variant	NEBL	GRCh38.p7	10:21066428	TAATGATTAAAAAAT[A/G]AAAGTTAAGAAGTAA	10529
rs117005614	snp	A/G	0.0360663	0.129354	intron-variant	NEBL	GRCh38.p7	10:20825395	GGCACAGTAGCTTAT[A/G]CCTGTAATCCCAGCA	10529
rs117006349	snp	A/G	0.00478085	0.0486577	upstream-variant-2KB, nc-transcript-variant	NEBL, NEBL-AS1	GRCh38.p7	10:21174707	TCCCAGAGGGGCCGA[A/G]GGTTGCACCGCGCCC	10529
rs117006608	snp	A/C	0.00478085	0.0486577	intron-variant	NEBL	GRCh38.p7	10:21158279	AACTTGGGATGTTTT[A/C]TCATCCCCAAAGCTT	10529
rs117007251	snp	A/G	0.0244538	0.107838	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21140521	TGAATGGATTAATGG[A/G]AATATAGTCTGTCCA	10529
rs117011338	snp	C/T	0.0707826	0.174302	intron-variant	NEBL	GRCh38.p7	10:21061023	CCAGGTGCCTGGAAA[C/T]GTGACCTTATTTGGA	10529
rs117012803	snp	A/G	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:21053203	GAATTCACTGACAAC[A/G]TTCTTTCCCCCCTAC	10529
rs117015293	snp	C/T	0.0170251	0.090679	intron-variant	NEBL	GRCh38.p7	10:20914470	GTCATTCCTTGGAAG[C/T]AAACATTCCTAATAC	10529
rs117023276	snp	A/G	0.152001	0.229992	intron-variant	NEBL	GRCh38.p7	10:20984754	CCACGGACTGGTACC[A/G]GTCCATGGCCTGCTA	10529
rs117036471	snp	G/T	0.0162398	0.0886349	intron-variant	NEBL	GRCh38.p7	10:21065601	AATGTCTTAACTCAT[G/T]ATTCTTAATGCAAAA	10529
rs117036966	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20963959	ACATAGGGAAACTCC[A/G]AGCCATTCATCAGCT	10529
rs117041269	snp	A/T	0.00636936	0.0560724	intron-variant	NEBL	GRCh38.p7	10:21077707	GTCTGTTGGTTCCTG[A/T]TATCTTTTTCCCTTC	10529
rs117050323	snp	C/T	0.0162398	0.0886349	intron-variant	NEBL	GRCh38.p7	10:21023136	AAGCTATAGTAACAA[C/T]TGAGCATGTTTTCTT	10529
rs117064248	snp	C/T	0.00517822	0.0506191	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20855577	TCTGCAAAAGAACTT[C/T]GAATGCGTGTCTTTC	10529
rs117070825	snp	A/G	0.00597247	0.0543191	intron-variant	NEBL	GRCh38.p7	10:21094885	GACTAGAACCCTCTC[A/G]TCATAGTTTCCCAGG	10529
rs117076342	snp	A/T	0.000798403	0.0199641	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20878081	TTTACTGTTTGGAGA[A/T]CATTTAATTTTGGGG	10529
rs117079045	snp	A/G	0.0185938	0.0946107	intron-variant	NEBL	GRCh38.p7	10:21054778	AAACTCTGCATTAAA[A/G]GAAATGTATGACTTG	10529
rs117079425	snp	A/C	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:21034530	TGCAATACATAGACT[A/C]TACTTATTTGACAAT	10529
rs117088537	snp	A/T	0.021333	0.101051	intron-variant	NEBL	GRCh38.p7	10:21123788	ACATATATAATTTTA[A/T]ATATTATATAAATAT	10529
rs117090480	snp	C/T	0.0193772	0.0965046	intron-variant	NEBL	GRCh38.p7	10:21018517	ACAAACACCAGCATT[C/T]TACACAAACTAAAAA	10529
rs117090993	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21107282	CAAAGGGTGCCCATT[C/T]GCTATGATATTGGCT	10529
rs117094896	snp	A/G	0.0189856	0.0955633	intron-variant	NEBL	GRCh38.p7	10:20788765	ATTTAAATATTTGAT[A/G]TCAACAGATGTTAAA	10529
rs117099501	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20950002	TATGACTCGTGTTCA[A/G]TTCCTTTCCCTCCTA	10529
rs117106387	snp	C/G	0.0154538	0.0865337	intron-variant	NEBL	GRCh38.p7	10:20818112	AAGCTAAAGCTCTCT[C/G]ACTCCTACCACCTCC	10529
rs117108791	snp	C/T	0.00398564	0.0444627	upstream-variant-2KB, intron-variant	C10orf113, NEBL	GRCh38.p7	10:21148193	AGAAAGGGAATAACA[C/T]GTGCAAATGTCCCAG	10529
rs117109958	snp	C/T	0.0310518	0.120672	intron-variant	NEBL	GRCh38.p7	10:21046099	AACATGGATAAAACC[C/T]GGAGGGCATTAAGTG	10529
rs117143564	snp	G/T	0.0111196	0.0737302	intron-variant	NEBL	GRCh38.p7	10:21071318	CCTTTTCTTAGTCAT[G/T]ACCACCCACAAAACC	10529
rs117148104	snp	A/G	0.0471551	0.14613	intron-variant	NEBL	GRCh38.p7	10:21047155	CATTTAAACTATGGG[A/G]GAAAAGCAGATCATC	10529
rs117148880	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21070824	TATTTTAAACTGGCA[C/T]ACATGTCTAAGAAGG	10529
rs117151191	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21118337	CTTCCCTGAGAAGGG[A/G]CAAAATGTTCACTCT	10529
rs117167205	snp	A/G	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:20965651	TGGAGGTTTGTATGC[A/G]GAACAGCGGTATGCC	10529
rs117173421	snp	A/C	0.0741063	0.177655	intron-variant	NEBL	GRCh38.p7	10:20838293	AAGAAGTTGATTTCA[A/C]CTCTCATGGATGACT	10529
rs117174695	snp	C/T	0.00993419	0.0697739	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20872082	AAATGGAAACCCTTA[C/T]TTTTTGAAAAGAACC	10529
rs117183409	snp	G/T	0.00716266	0.059414	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20856237	GTAACGTATGACTTT[G/T]CTGTGTTTTCTCTGT	10529
rs117185779	snp	C/T	0.0460142	0.144533	intron-variant	NEBL	GRCh38.p7	10:21065970	TCTTCAACCTGGTTA[C/T]GTGTTAGCTGTCCTC	10529
rs117193526	snp	A/T	0.0368353	0.130617	intron-variant	NEBL	GRCh38.p7	10:20952475	GAACTGGAAATAGGA[A/T]ATAGGAGGAAGTTTT	10529
rs117258655	snp	G/T	0.0260105	0.111035	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21137359	TAGCCACAGCTATTC[G/T]TGCATGCTTAGTCTT	10529
rs117266296	snp	A/G	0.0165278	0.0893908	intron-variant	NEBL	GRCh38.p7	10:20804805	ATATGGGTCTTGTAC[A/G]CAATGATGAAAATTT	10529
rs117272444	snp	A/T	0.0364509	0.129988	intron-variant	NEBL	GRCh38.p7	10:21025108	TAAGAATGTAGGAAG[A/T]AGACACAGGGCATGA	10529
rs117275901	snp	C/T	0.0271762	0.113356	intron-variant	NEBL	GRCh38.p7	10:20799719	GTCACCAATCAGTAG[C/T]CAGAAAACCGAAGCA	10529
rs117284331	snp	C/T	0.00597247	0.0543191	intron-variant	NEBL	GRCh38.p7	10:21072610	AGCACAGGAAGGGTA[C/T]GCCCAGGGGGATCCA	10529
rs117285068	snp	A/C	0.0444908	0.142359	intron-variant	NEBL	GRCh38.p7	10:21042194	AGGACTCTGTATTTA[A/C]CGTCTCATTTAATCC	10529
rs117292765	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20834482	AATCATGGCAATCCC[A/G]TTTCCCTGGCCAGTG	10529
rs117294960	snp	A/G	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:21163289	AAGTTTTCAGAAAAT[A/G]ACTGTGGTGGCAGGA	10529
rs117305326	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20799016	TGAACGAATACTTGC[A/G]AACAATGTACAATGT	10529
rs117305544	snp	A/G	0.00636936	0.0560724	intron-variant	NEBL	GRCh38.p7	10:20837769	AGCTGCTGACTTTAA[A/G]TTGCAGCCAATGCTC	10529
rs117339904	snp	A/G	0.0150606	0.0854603	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20898670	GCATATTGACATACT[A/G]GAAGTTCTGAGAAGA	10529
rs117347142	snp	A/G	0.0275645	0.114116	upstream-variant-2KB, nc-transcript-variant	NEBL, NEBL-AS1	GRCh38.p7	10:21174656	CGCACCCAGGCCCAA[A/G]GGCCGGGAGATCCGC	10529
rs117365503	snp	A/C	0.046775	0.145601	intron-variant	NEBL	GRCh38.p7	10:21056029	AACTATATTCAGAGT[A/C]CTGCCTTAACATTAG	10529
rs117367216	snp	A/G	0.021333	0.101051	intron-variant, nc-transcript-variant	NEBL	GRCh38.p7	10:20818937	ATCTGGAGATATTCC[A/G]TTTATCATCATCGTT	10529
rs117367962	snp	A/G	0.0448719	0.142907	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21134025	GGATGTCAGGAGTTC[A/G]AGGTCAGCCTGCCTA	10529
rs117394109	snp	A/G	0.0162398	0.0886349	intron-variant	NEBL	GRCh38.p7	10:21100512	TCTGAGGATGAGGCC[A/G]TCCAGTTTCCCGTGA	10529
rs117401705	snp	A/T	0.021333	0.101051	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21140844	ATATCTAACGCATGC[A/T]TGGCTTAAAACCTAG	10529
rs117406371	snp	A/G	0.0111196	0.0737302	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21139880	CATGGTCAGGCACTG[A/G]TGGCTCACGCCTGTA	10529
rs117417416	snp	C/T	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:20913943	TACATATTTTGGAAA[C/T]GGTCATTCTTGAAAA	10529
rs117435074	snp	C/T	0.0360663	0.129354	intron-variant	NEBL	GRCh38.p7	10:20811356	GGCCTGGAAGTAAGC[C/T]GTACAGACTTTAGCA	10529
rs117450293	snp	A/G	0.00914312	0.0669923	intron-variant	NEBL	GRCh38.p7	10:21110498	AGTAATGTCATTTCT[A/G]TCATCCCTGGTATTG	10529
rs117469307	snp	C/G	0.0744748	0.178019	intron-variant	NEBL	GRCh38.p7	10:20836559	CTATTGAGACAGACA[C/G]ATAGGAGGGGGTCAC	10529
rs117488867	snp	A/G	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:21151884	CTATAGAACATATCC[A/G]TTTCTAATATTTTAC	10529
rs117494757	snp	A/G	0.00993419	0.0697739	intron-variant	NEBL	GRCh38.p7	10:21010034	GTTTAAGGCCATTAC[A/G]AGACAGTAGTGTCTA	10529
rs117516140	snp	A/G	0.0345262	0.126772	intron-variant	NEBL	GRCh38.p7	10:20799276	TTCTCCTGCCTCAGC[A/G]TCCTAAGTAGTGGGG	10529
rs117523887	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21020384	ATTCTCATGGCTCTG[C/T]CGCCCAGACATCCTC	10529
rs117535559	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21082207	CTTGCAGGTTAGTGG[A/C]AACTGAAGGAACATG	10529
rs117541443	snp	A/C/T	0.0349115	0.127424	intron-variant	NEBL	GRCh38.p7	10:20798334	AAAGTCAGGAACCAA[A/C/T]CCCCACAACCTACAC	10529
rs117549860	snp	A/G	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21133584	GGGAATCTTCATAGA[A/G]TTGGAAGGATTATGT	10529
rs117552075	snp	A/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20822964	TTGGAGTCTCCAATG[A/T]CTATGATTCCACTCT	10529
rs117567360	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21117459	CCTCTGAACTCTGTC[G/T]CCTCAACTTAGGGTA	10529
rs117580595	snp	C/T	0.0142736	0.0832652	intron-variant	NEBL	GRCh38.p7	10:20936415	CTATTGCAAATGGAA[C/T]CTAAAAAATGGTGGA	10529
rs117583060	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20947418	TGTCAAACTCACCTG[C/T]TCCCCTCTTCTTGTG	10529
rs117588303	snp	A/G	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:21168067	TCGTTCTATCAAAAG[A/G]TCAAAATTTAAATAT	10529
rs117595353	snp	A/T	0.0463947	0.145069	intron-variant	NEBL	GRCh38.p7	10:21066423	CATGCTAATGATTAA[A/T]AAATAAAAGTTAAGA	10529
rs117597682	snp	C/T	0.0142736	0.0832652	intron-variant	NEBL	GRCh38.p7	10:21115539	GTCTAGGTGAGAGTT[C/T]TTTTTCTTTCAGTGC	10529
rs117612551	snp	A/C	0.0471551	0.14613	intron-variant	NEBL	GRCh38.p7	10:21040427	CTGTTTCTGGTGAGG[A/C]CTCAGTAAGCTTCCA	10529
rs117617957	snp	A/T	0.0711525	0.174681	intron-variant	NEBL	GRCh38.p7	10:21061495	ACATCATATATGATA[A/T]ATCATATATTACATT	10529
rs117646116	snp	C/T	0.029116	0.117091	intron-variant	NEBL	GRCh38.p7	10:20803487	AAAAAATTTTAACTA[C/T]ATTTTGTTTTTAAAA	10529
rs117647472	snp	C/T	0.0123036	0.0774623	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20864536	ACTCTCTGTTCCCAT[C/T]CTTTCATCAGACAGG	10529
rs117651577	snp	A/C	0.0103295	0.0711199	intron-variant	NEBL	GRCh38.p7	10:20929556	ATACATATACACATA[A/C]ACCATGGAATACTAC	10529
rs117659071	snp	A/T	0.046775	0.145601	intron-variant	NEBL	GRCh38.p7	10:21060995	CCGAGAAAGATTTGT[A/T]GAAGTCCTAACACCA	10529
rs117660503	snp	C/T	0.00874735	0.0655527	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20866421	TGGGGAAAAATTACA[C/T]ATATGAACACATTAT	10529
rs117686649	snp	A/G	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:21105173	GAAGAATATTGGCCT[A/G]TAATAATCTTCATTT	10529
rs117688245	snp	A/C	0.00318978	0.0398085	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21134405	AACAGTGTTAAAAAC[A/C]TTTTGTAATGCTAAA	10529
rs117692689	snp	A/G	0.00755907	0.0610114	intron-variant	NEBL	GRCh38.p7	10:21024362	TTCAATTTAGTATTA[A/G]TAACGAAAATAATAA	10529
rs117693196	snp	A/C	0.00438332	0.0466095	intron-variant	NEBL	GRCh38.p7	10:20903668	TGGTATGCATACACC[A/C]CGGAATACAACTCAG	10529
rs117698119	snp	A/T	0.0146672	0.084371	intron-variant	NEBL	GRCh38.p7	10:21075102	TGAGCCACGACACCC[A/T]GCCCAGAATTATTTT	10529
rs117705632	snp	C/T	0.0399052	0.1355	intron-variant	NEBL	GRCh38.p7	10:20968394	TACATACCCATAGTC[C/T]CAGCTACTAGGGAAG	10529
rs117706487	snp	C/T	0.021333	0.101051	intron-variant	NEBL	GRCh38.p7	10:21123778	AAAATCTTCAACATA[C/T]ATAATTTTATATATT	10529
rs117719529	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20867368	ACCTTTCATCATTTA[C/T]ATCTCTCCACTTTGA	10529
rs117724340	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20899544	CAAATTTTCCATTTG[A/G]GATTCTAGAATCAGA	10529
rs117725304	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20780849	CATTCCTGGTTTGCC[A/G]TCATTTAAGTAGTTT	10529
rs117737226	snp	A/G	0.00835141	0.0640778	intron-variant	NEBL	GRCh38.p7	10:21081371	CCATGGGGATGTGAG[A/G]CTTGTTATGCACAGG	10529
rs117744561	snp	C/T	0.0337553	0.125452	intron-variant	NEBL	GRCh38.p7	10:21056638	CATGTACACCCATAT[C/T]GTCATGTCAAAAGAA	10529
rs117754139	snp	C/T	0.0327778	0.123752	intron-variant	NEBL	GRCh38.p7	10:20801416	TGGCCAGGCTAGTCT[C/T]GAACTCCTGACCTCA	10529
rs117756100	snp	A/G	0.095934	0.196885	intron-variant	NEBL	GRCh38.p7	10:21036374	TGGGAGGGTCATTTG[A/G]TCCTGGGAGGTCGAG	10529
rs117800812	snp	A/G	0.00874735	0.0655527	intron-variant	NEBL	GRCh38.p7	10:21017115	TCCAAGACCTATTCC[A/G]TACCAGCTAAGTGTG	10529
rs117818160	snp	C/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21159852	CGTTGGCAAAACTCC[C/T]GGATCTTACGTATCT	10529
rs117820715	snp	C/T	0.0479149	0.147179	intron-variant	NEBL	GRCh38.p7	10:21029003	CCGCTCCCAACATGG[C/T]GGCCTCAGCAAAAAA	10529
rs117843784	snp	A/G	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:21046384	TTTGTAGTGTTATAC[A/G]AGGTAATACATATGT	10529
rs117850381	snp	A/G	0.077417	0.180873	intron-variant	NEBL	GRCh38.p7	10:21047102	TTCCAGATGTACTGA[A/G]AGTCAATCACTGACT	10529
rs117850894	snp	C/T	0.0715223	0.175059	intron-variant	NEBL	GRCh38.p7	10:21122441	AGTCTCACTTCATTT[C/T]CTTCTCTCCTCCATA	10529
rs117859219	snp	A/T	0.0107246	0.0724382	intron-variant	NEBL	GRCh38.p7	10:21021039	CCACCCCTCCATAAC[A/T]CAAGTTCCTCCCCTG	10529
rs117862654	snp	G/T	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:21171724	CTAATTGCTATTCTA[G/T]GCTAGCAGCATGCCT	10529
rs117863732	snp	A/G	0.0197687	0.0974348	intron-variant	NEBL	GRCh38.p7	10:20932741	ACCATTTTATTTGTC[A/G]ATACTAATCGTTGTG	10529
rs117870370	snp	A/G	0.0130921	0.0798413	intron-variant	NEBL	GRCh38.p7	10:21110208	CTTGTGCCCACTTCT[A/G]TTTACTGAAAGAGTC	10529
rs117880040	snp	A/G	0.0356815	0.128715	intron-variant	NEBL	GRCh38.p7	10:21032593	TTTTTTTAAAAGACG[A/G]TGAATTAGAGCACGT	10529
rs117880291	snp	C/T	0.0119091	0.0762411	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20866442	AACACATTATTCCTA[C/T]TATGTTCTCTAAGCA	10529
rs117907337	snp	A/C	0.0345262	0.126772	intron-variant	NEBL	GRCh38.p7	10:20795157	TGTTGAGCAGAGAAG[A/C]TTCTAGGAGTAAGAA	10529
rs117907421	snp	A/G	0.0103295	0.0711199	intron-variant	NEBL	GRCh38.p7	10:20893871	GGTCCTAAGCTATCA[A/G]CTACAGGTCAGAAAT	10529
rs117934241	snp	G/T	0.0314385	0.121371	intron-variant	NEBL	GRCh38.p7	10:20810301	TTTGATTATAGTTTC[G/T]GATTCAGGACATGTG	10529
rs117937050	snp	G/T	0.0146672	0.084371	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20876631	AATACTTCTTTCTAA[G/T]ACACATTGAATCGAC	10529
rs117984816	snp	A/G	0.0150606	0.0854603	intron-variant, upstream-variant-2KB	NEBL, NEBL-AS1	GRCh38.p7	10:21173269	GCAGGGATTATTCTT[A/G]GCAATGCGGCAGCGG	10529
rs117988232	snp	C/T	0.0729998	0.176553	intron-variant	NEBL	GRCh38.p7	10:21049231	ACCAAAGGCTGGGTA[C/T]CATGGCCTAGCCAAG	10529
rs118001445	snp	C/G	0.0244538	0.107838	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21133139	TTTTGAGTTAATTTT[C/G]TATGTGTGTGAGGTG	10529
rs118002542	snp	C/G	0.00438332	0.0466095	intron-variant	NEBL	GRCh38.p7	10:21084595	GAGCAAGACTCTGTC[C/G]CAAAAAAAAAATAAA	10529
rs118010113	snp	A/G	0.0119135	0.0762987	intron-variant	NEBL	GRCh38.p7	10:20984893	TTCAGATCAGCGGTG[A/G]CATTAGATTCTCATA	10529
rs118012287	snp	A/G	0.0225045	0.103662	intron-variant	NEBL	GRCh38.p7	10:21156751	ATCTGAGAAACTTTC[A/G]TGAGAAAATTAATAA	10529
rs118027505	snp	C/T	0.0228947	0.104514	intron-variant	NEBL	GRCh38.p7	10:20890956	CCATAAATACTTAAA[C/T]TGAAAAAGTGTTCCT	10529
rs118039142	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21121700	TGAAATAGCGATGCC[A/G]TCTCCGTTTAAATGT	10529
rs118046652	snp	A/G	0.031825	0.122064	intron-variant	NEBL	GRCh38.p7	10:21088929	GAGGATGGGCAGTTA[A/G]TGAACCACGCGAGGC	10529
rs118084218	snp	A/C	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:21057942	TCAGTAAATCATATA[A/C]TCGTGAACACCAGCT	10529
rs118089052	snp	A/T	0.0165278	0.0893908	upstream-variant-2KB, intron-variant	C10orf113, NEBL	GRCh38.p7	10:21148365	AAAGTATGTGGACTT[A/T]GGTCCGTGGTTCCCA	10529
rs118100017	snp	A/G	0.0123036	0.0774623	intron-variant	NEBL	GRCh38.p7	10:21048302	CCTTCAAGGAGAGTC[A/G]CAGACCCACAGCATG	10529
rs118105259	snp	A/C	0.021333	0.101051	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20873666	GTATGACGGTATGAA[A/C]TTTTTCAAACAATCA	10529
rs118112465	snp	C/T	0.0162398	0.0886349	intron-variant	NEBL	GRCh38.p7	10:21042258	TTCCTCACTTTGGGA[C/T]TGAGGAACGTACGTC	10529
rs118113810	snp	C/T	0.046775	0.145601	intron-variant	NEBL	GRCh38.p7	10:21052270	CACTTCATGAGTCAA[C/T]ACTGGGAAGAGAGAG	10529
rs118126704	snp	A/G	0.0221141	0.102801	intron-variant	NEBL	GRCh38.p7	10:20934559	GTGCTATCCACGATG[A/G]GCCCGCTCTTTGCCT	10529
rs118130458	snp	A/G	0.0475351	0.146656	intron-variant	NEBL	GRCh38.p7	10:21032946	ACCCTACTATGAAAT[A/G]CTTATCGGCTATTGA	10529
rs118131868	snp	C/T	0.077417	0.180873	intron-variant	NEBL	GRCh38.p7	10:21036840	GGCCTGGAGGTGACT[C/T]GGGTATCTCCACATC	10529
rs118132570	snp	A/G	0.0547245	0.156101	intron-variant	NEBL	GRCh38.p7	10:21155992	ATTGGGAACAGCCCT[A/G]CAGTCTCCAGCAGGG	10529
rs118134181	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20795443	GAAATTCACCCACTT[C/T]TGGAAAAGCAAACTC	10529
rs118143296	snp	G/T	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20919412	TACCATTTCAAACTT[G/T]ATGTTTCTATAATCA	10529
rs118144590	snp	C/T	0.0158469	0.0875917	intron-variant	NEBL	GRCh38.p7	10:21076658	AATGTGATATACACA[C/T]ATGATCAGCTACTAT	10529
rs118159357	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21162578	TAAAGTAGTCCCTTC[A/G]AGGAGCAAAGCTCTT	10529
rs118162870	snp	C/G	0.0103295	0.0711199	intron-variant	NEBL	GRCh38.p7	10:20936504	CCATGTCTTTTCTGT[C/G]CTGAATCACATAATT	10529
rs118163915	snp	G/T	0.0165278	0.0893908	intron-variant	NEBL	GRCh38.p7	10:21067480	AAGAGAAAGCAGGAG[G/T]AGGGAGGAGAACAAG	10529
rs118187770	snp	C/T	0.0759472	0.179459	intron-variant	NEBL	GRCh38.p7	10:21033992	GCAAAATAGCGAAAA[C/T]TCATCTCTACAAAAA	10529
rs118188230	snp	C/T	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:21085204	ATGCTAATCTTGAAA[C/T]ATTTATATTTCTTCC	10529
rs137875835	snp	C/T	0.00914312	0.0669923	intron-variant	NEBL	GRCh38.p7	10:20946660	AGAGACGAGGTTTCA[C/T]CACGCTGTTGGCCAG	10529
rs137875841	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20912834	CTCCTTCACTTTCCC[A/T]ATGCCATGCTGAACT	10529
rs137890117	snp	A/G	0.00199481	0.0315187	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20856227	CATGAAATAAGTAAC[A/G]TATGACTTTGCTGTG	10529
rs137893238	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20792410	GGACAAAGAACCCCT[A/G]TTTAGACAATCAGAG	10529
rs137903071	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21107260	ATTCTTGTCTTGTGA[C/T]GGTTTTCAAAGGGTG	10529
rs137912499	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20974407	TACAGGCATGCTCCA[C/T]CACATCCAGCTAATT	10529
rs137913074	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20866971	CAAAAATAAATTCCT[C/T]TTCAAGAATGTTTAT	10529
rs137917266	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20916161	TTGATGAGTGCAGAC[C/T]GCTAAATGTGAGAAT	10529
rs137923051	in-del	-/C	0.039522	0.134904	intron-variant, downstream-variant-500B	NEBL, LOC102725112	GRCh38.p7	10:20885253	TCTTCTACTTTCTTG[-/C]CCCGCTTATTAGGTA	10529
rs137923638	snp	C/G	0.00358779	0.0422022	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20858694	ACTATGCTTTGTGGA[C/G]ATCTGAGGATTTTGA	10529
rs137939345	snp	A/G	0.00874735	0.0655527	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21144663	CCCGGGGAGTTGGAG[A/G]TTGCAATGAGCCGAG	10529
rs137939380	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21104910	TCCATCTATGCCCAG[C/T]TTGCTCAGAGTTATT	10529
rs137948799	snp	A/G	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:21035553	TCCTGGCCATCGATT[A/G]TATAATTAAACTAAA	10529
rs137973321	snp	C/T	0.00424773	0.0458893	intron-variant, missense, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20868744	CTTTATTCATTATTC[C/T]TTGTCCTTTCTTGTA	10529
rs137978366	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20977989	AAGGGAATAGATTAC[A/G]TTGAAAATTAATCTT	10529
rs137996321	snp	G/T	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:20950468	CTCTTCCCTTCCTTC[G/T]GCCTCTTCTCCCTCA	10529
rs138006805	snp	C/G	0.00517822	0.0506191	intron-variant	NEBL	GRCh38.p7	10:21048429	AAGGGCCATTCTACT[C/G]TTAGACATAATAAAT	10529
rs138007135	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21007384	AGATTTCTTTGCTAG[C/T]AAAGGTTTGAAACCA	10529
rs138010324	snp	C/T	0.00438332	0.0466095	intron-variant	NEBL	GRCh38.p7	10:21019942	AGGACAATTCAAGAC[C/T]GGGAACAGTACAGAT	10529
rs138011657	snp	C/T	0.00478085	0.0486577	intron-variant	NEBL	GRCh38.p7	10:21084844	CGGTTGCTGCCAAGA[C/T]TCAACATGACTTTAC	10529
rs138040818	snp	C/T	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:20920450	AGCGACACACTGGAG[C/T]TGTCAAAATGTATAA	10529
rs138045393	snp	C/T	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:20836629	GCGCTGGGGTGGAGC[C/T]ACAGAAGTTCCGGCA	10529
rs138045639	snp	C/T	0.00279162	0.0372561	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20863123	GTTAAGCTACAGTGA[C/T]GGCATTGTAGCTCCC	10529
rs138046620	snp	C/G	0.0119091	0.0762411	intron-variant	NEBL	GRCh38.p7	10:20943291	CACGTCCTTTGTAGG[C/G]ACATGGATGAAGCTG	10529
rs138050042	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20799728	CAGTAGTCAGAAAAC[C/T]GAAGCAGTGGCTAAA	10529
rs138053288	in-del	-/TTTTC	0.182614	0.240747	intron-variant	NEBL	GRCh38.p7	10:21105190	ATAATCTTCATTTCT[-/TTTTC]TTTTCTTTTATATTT	10529
rs138077240	in-del	-/AT	0.219049	0.248077	intron-variant, downstream-variant-500B	NEBL, LOC102725112	GRCh38.p7	10:20885068	ATTGACTTTAAGATA[-/AT]AGTTTGTTTTAATAA	10529
rs138107810	snp	A/G	0.00835141	0.0640778	intron-variant	NEBL	GRCh38.p7	10:21052584	CACCGATTGGTCAGC[A/G]GGGTATAGAAGCTCT	10529
rs138110708	snp	C/G	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:20807897	TTAATCCATCAGCCT[C/G]GATACAGAAAACAGA	10529
rs138118635	snp	C/T	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:20982679	GGGATATCTTTTAAT[C/T]ACTTAGCATACCATA	10529
rs138122667	snp	A/G/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20954380	TGGGTCTGTATAGAA[A/G/T]AAAAGACACAGCCCA	10529
rs138139264	snp	C/T	0.00795532	0.062565	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20878958	GTTGGAAAGAGCCTC[C/T]CGGGGATCCGTGTAA	10529
rs138142742	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20811663	TTAGCACCCTGGTTT[G/T]GTAAAGACATTACCC	10529
rs138143925	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21054653	AGGAAGGACCATAGC[A/C]CAAATGTATTTTTTC	10529
rs138148717	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20987456	TCACCTTTCTTTGTG[C/T]TTTCTCAGTGACCTC	10529
rs138148754	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20924597	GCTCTGGTCATTTCT[C/G]ATGAAATGAGTGAGA	10529
rs138157265	snp	G/T	0.00159617	0.0282053	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20868276	AAGCACTTGAAAATT[G/T]GGAAAATTAATATTT	10529
rs138159238	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20947765	AGCAGATGGAAGGAC[A/G]GCTTCATAGCAGACT	10529
rs138160972	snp	A/C	0.0103295	0.0711199	intron-variant	NEBL	GRCh38.p7	10:20892327	CATTCTGTCTTCCAC[A/C]TTTTTCTTTCTCAAT	10529
rs138168672	snp	C/T	0.0150606	0.0854603	intron-variant	NEBL	GRCh38.p7	10:20805836	CCAGGCTGAGTGACA[C/T]AGCGAGACTCCGTCT	10529
rs138174414	in-del	-/TGAG	0.0240643	0.107019	intron-variant	NEBL	GRCh38.p7	10:21089162	TTTGAGTTTTCTGCT[-/TGAG]CGGAGTCTAGAGGAT	10529
rs138174512	snp	A/G	0.0107246	0.0724382	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21145806	TGTAGGGAAATGCCA[A/G]GGGCTCCGGCAGCTG	10529
rs138176832	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21113459	TCTGGATGACTGACC[A/G]GGAGGCTATTCAGAT	10529
rs138206930	snp	A/C/G	3.31138e-05	0.00406891	intron-variant, synonymous-codon, nc-transcript-variant	NEBL	GRCh38.p7	10:20809894	TGTGCGCCAAACTTT[A/C/G]AGGTCTTTTGCCAAA	10529
rs138218835	snp	C/T	0.00260955	0.0360273	intron-variant, splice-acceptor-variant	C10orf113, NEBL	GRCh38.p7	10:21126159	GTCCGTTCTTCAAGC[C/T]TGGTACCCCCCATAG	10529
rs138227957	snp	A/G	0.0142736	0.0832652	intron-variant	NEBL	GRCh38.p7	10:21061231	GAGATGTGGCATTAT[A/G]TATTGTGATATATTA	10529
rs138244344	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20908131	GAGCTTTATATACAG[A/T]AACCCATGTGATCTT	10529
rs138253500	in-del	-/TTT			intron-variant	NEBL	GRCh38.p7	10:21003004	TTTTCATTATGTGGC[-/TTT]TTTTTTTTTTTTTTT	10529
rs138254350	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20958556	CCTAACATTCAATTT[C/G]ATAAGCAACCAAACC	10529
rs138256095	snp	C/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20903799	ATGTTGTCTGTCACT[C/G]ATAAGTGGCAGCTAA	10529
rs138258992	snp	A/G	0.0349115	0.127424	intron-variant	NEBL	GRCh38.p7	10:21049029	AAATAAATAAATAAA[A/G]AGACTGTCTAGAAGA	10529
rs138264025	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20935002	AAGCAAAGTGCCACA[A/C]GATTTTATTTATTCG	10529
rs138265758	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20816208	AGAGAGTACATGTGT[C/T]CAAATCACTGTGGAT	10529
rs138266971	snp	G/T	0.00676609	0.0577691	intron-variant	NEBL	GRCh38.p7	10:21158681	AGATGCCACCCTCTG[G/T]ATGGACAGATTCCAA	10529
rs138269177	snp	A/G	0.00358779	0.0422022	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20850790	ATATAGATATGTATC[A/G]TATATATGGGGTTAT	10529
rs138273932	snp	C/T	0.00993419	0.0697739	intron-variant	NEBL	GRCh38.p7	10:20900327	AATTATTCAACCCCT[C/T]ACTACCTCTAATTCT	10529
rs138282037	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20838097	AATTTTTACTTTCAA[A/G]GCTTATTATTTAAGA	10529
rs138302427	snp	C/T	0.00199481	0.0315187	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20855629	CCTCCTAGTGGGAGA[C/T]ACACGGAGTAACACA	10529
rs138310534	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21171741	CTAGCAGCATGCCTA[C/T]ACAAAAGCCTTCCAA	10529
rs138313883	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20802992	CTTTGATAACCCGGA[C/G]CAAGTCGTGAGAGCA	10529
rs138318287	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20841752	AAGATTGAGTTATTG[C/T]CCAGTTGGAATTCAC	10529
rs138319608	snp	C/T	3.30945e-05	0.0040677	intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20831203	TGACCAACCTGGCTA[C/T]AGATTTCAGATGTCC	10529
rs138319856	snp	C/T	0.00716266	0.059414	intron-variant	NEBL	GRCh38.p7	10:21104799	AACATCCTCACCCTG[C/T]TCCTCATCTCAGGGG	10529
rs138323077	snp	A/T	0.00716266	0.059414	intron-variant	NEBL	GRCh38.p7	10:21086730	TGCAGTGAGCCATGA[A/T]CGTGCCACTGCACTC	10529
rs138323633	in-del	-/C	0.121717	0.214577	intron-variant, downstream-variant-500B	NEBL	GRCh38.p7	10:20813391	AGGTAACAATATATA[-/C]CACTTTTAATATAAT	10529
rs138327181	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21155581	TATACATAAGTACTT[C/T]GGAAATCTTGAGTAC	10529
rs138333140	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21159671	GGTCTGCCATGCAGC[A/G]GGGCCACCTGTTTCC	10529
rs138341019	snp	C/T	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:21065962	CACACCTCTCTTCAA[C/T]CTGGTTACGTGTTAG	10529
rs138345278	snp	A/G	0.0107246	0.0724382	intron-variant	NEBL	GRCh38.p7	10:20999771	CCCGCTTTAACTGCC[A/G]TGGAGGCTGTGAAGC	10529
rs138348210	snp	A/G	0.0107246	0.0724382	intron-variant	NEBL	GRCh38.p7	10:20912245	GAGGAATGCTCACAG[A/G]CGTGGCTTGCAAGAA	10529
rs138371852	snp	A/C	0.00517822	0.0506191	intron-variant	NEBL	GRCh38.p7	10:21099691	AGCACATGTTCTTCC[A/C]TTTTATCTCCATGAA	10529
rs138392507	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21032591	AATTTTTTTAAAAGA[C/T]GGTGAATTAGAGCAC	10529
rs138392598	snp	A/C	0.0107246	0.0724382	intron-variant	NEBL	GRCh38.p7	10:20989627	TATTACAAAAACTTC[A/C]TGAAGTACTAGCATG	10529
rs138393670	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20937372	TATTATCATTCCCAT[C/G]AGAGATGTAGGAGAA	10529
rs138399191	snp	C/T	0.00119737	0.0244387	intron-variant, downstream-variant-500B	NEBL, LOC102725112	GRCh38.p7	10:20880615	CAACATAAAGGCATT[C/T]GGCAAGGTGTTAATG	10529
rs138421324	snp	C/T	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20796704	TTAGATTCGAATTGC[C/T]ACTTCCATTTTTTTC	10529
rs138424319	in-del	-/AT	0.105214	0.203807	intron-variant	NEBL	GRCh38.p7	10:21043800	TTATATTTATTCAAC[-/AT]AGATGCATCAGACTA	10529
rs138426084	snp	G/T	0.00874735	0.0655527	intron-variant	NEBL	GRCh38.p7	10:20993359	AATGTAAAAGGAGCT[G/T]ATTAATCCAAATGAA	10529
rs138427051	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20847322	AACATCTAATAGTCA[A/G]TGACTATAATTAAAG	10529
rs138432675	snp	A/T	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:21039119	CCTTGTAGATTCTGG[A/T]TATTAGACCTTTGTC	10529
rs138433669	snp	A/G	0.0119091	0.0762411	intron-variant	NEBL	GRCh38.p7	10:21107592	TTATTGAGGATTTTT[A/G]CATCGATGTTCATCA	10529
rs138434020	snp	C/T	0.0240643	0.107019	intron-variant	NEBL	GRCh38.p7	10:20932169	TCCAAACCACCATAT[C/T]GTACCTGTCTCCCGT	10529
rs138438052	snp	C/G	0.0158469	0.0875917	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20784323	TGGACTGCAGACTCT[C/G]GATGAAATTTCAAGA	10529
rs138474409	snp	G/T	0.00557542	0.0525036	intron-variant	NEBL	GRCh38.p7	10:20966623	CCAAGTTCATGCAGG[G/T]TGACAGCCTGGACAC	10529
rs138475178	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20795615	TCCCATTGCCAATAC[C/T]AACCTATTTTATCCA	10529
rs138475771	snp	A/G	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21035303	ATGCCCAGCCCCCAA[A/G]CTATTTATTCTGATG	10529
rs138477324	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21003528	ATTATTCTTCAAAGA[C/T]GGAAACCATGAATTT	10529
rs138493196	snp	C/G	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20969326	AACATAATTAAAAAG[C/G]ATTAAAAATCATGTC	10529
rs138495120	snp	C/G	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:21038166	ATTTTCAATCAAGTA[C/G]CAACTCAAGGTTATA	10529
rs138498325	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20879337	TGCATGGCTGTGCTC[A/G]GTAAGTGGTAGTTAT	10529
rs138502854	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21096736	CCCAAGCTAGTCTCA[C/T]ACTCCTGGTCTCAAG	10529
rs138507474	snp	A/G	0.00676609	0.0577691	intron-variant	NEBL	GRCh38.p7	10:21073744	AACCTGTTAACATAC[A/G]TGGCTAAAAGGAAGA	10529
rs138516643	snp	C/G	0.00478085	0.0486577	intron-variant	NEBL	GRCh38.p7	10:20791832	AAAGAAGTTCACTGG[C/G]GGGGATGTACGCAGA	10529
rs138521414	snp	A/T	0.00199481	0.0315187	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21127346	ATGATGGAATTAAAA[A/T]ATTTCCAGTTTGTGA	10529
rs138544538	snp	A/T	0.000798403	0.0199641	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21133848	AGCTTAGGAACCACT[A/T]GATGCTGATGGTCAT	10529
rs138550719	snp	A/G	0.00318978	0.0398085	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21141357	TTATTTAGGGGCAAC[A/G]AGACATCTTATCTGC	10529
rs138556214	snp	C/G/T	0.000798403	0.0199641	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20860245	TCCAAATAAAGAGCA[C/G/T]GACGTGTACCACAGT	10529
rs138558829	snp	A/G	0.00597247	0.0543191	intron-variant	NEBL	GRCh38.p7	10:21051753	TCCTAACTATATGTT[A/G]TCTACAGGAGACTCT	10529
rs138571776	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20982041	TAGAGTCTTCCAGAT[C/T]ACATTTCTCCTGTAT	10529
rs138589848	snp	C/T	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:20947184	GTGAGTTTCAAAGAG[C/T]CATATGTCGAAAACA	10529
rs138594873	snp	C/T	0.00914312	0.0669923	intron-variant	NEBL	GRCh38.p7	10:20892228	GCCTGGGGAGCCACA[C/T]TCTCTGTGACTTTAG	10529
rs138596697	snp	G/T	0.00358779	0.0422022	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21138401	AGAGGGAAGAAATCT[G/T]TATAATAAATGGACT	10529
rs138604318	snp	A/G	0.00018655	0.00965609	intron-variant	NEBL	GRCh38.p7	10:21069971	CGGCTTAGGGACTGC[A/G]CCCCTGGAGCCAGAA	10529
rs138607010	snp	A/G	0.0174175	0.0916809	intron-variant	NEBL	GRCh38.p7	10:20805722	GCCAAGTGTGGTGGC[A/G]TGCACCTGTAATCCC	10529
rs138608099	in-del	-/AC			intron-variant	NEBL	GRCh38.p7	10:21098180	TGTAGGAGGATAGCA[-/AC]ACACACACACACTCA	10529
rs138616930	snp	C/T	0.00358779	0.0422022	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21145179	TATTCTCTTACATTT[C/T]GTCTGGGACAGTAGG	10529
rs138636379	snp	A/C	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20919900	CTGCAAGCAAAAGCA[A/C]GGTAGCAGGGGGAAA	10529
rs138638432	snp	C/G	0.00199481	0.0315187	intron-variant, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20884719	TCCTGTGACCACCGT[C/G]GATGAAACATAGACT	10529
rs138644815	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20821475	ATTTGCATGCCCCTT[C/T]CTCTATGTCATACCA	10529
rs138647563	snp	G/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20924114	TCTAAATTGGTGATT[G/T]TCAGCTAGGGAGATT	10529
rs138658414	snp	A/T	0.00159617	0.0282053	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20867607	CTGTTATCCTTATGT[A/T]GTATATAGAGTCTCC	10529
rs138679057	snp	A/T	0.00438332	0.0466095	intron-variant	NEBL	GRCh38.p7	10:20888779	CACAATAGATTGCTC[A/T]CTTCCAATATTTTGC	10529
rs138681968	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20824332	CCATGCAGACTGTCA[C/T]AAAGAAACAGTACCT	10529
rs138693895	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20927081	GAGGAGTTTCAACGC[A/G]ACTGCATGTGGAGAG	10529
rs138699882	snp	A/T	0.0123036	0.0774623	intron-variant	NEBL	GRCh38.p7	10:20905629	CCAAACCATGTCACC[A/T]ATAAATGACCAGATC	10529
rs138711805	snp	C/T	0.0352966	0.128072	intron-variant	NEBL	GRCh38.p7	10:21080530	CAATATGAAGTTAGC[C/T]TTGGATCTTAGGGTC	10529
rs138714118	snp	A/G	0.0107246	0.0724382	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20846036	ATGAAAGGTGGATGC[A/G]ACGGTGATAGCTGGG	10529
rs138715725	snp	C/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20971200	TTGCCAAAATGGTAG[C/G]ACTGGCAAAAATACT	10529
rs138722717	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21015380	GAGAAGGCTCCAGAG[C/T]CCTGGTTCAGAGTAC	10529
rs138728687	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20833967	TATGCTTTGGTTGGC[A/G]CCATTTGAAGATTGG	10529
rs138735770	snp	C/G	0.00597247	0.0543191	intron-variant	NEBL	GRCh38.p7	10:21150001	TTTTTCCACTCAGAA[C/G]TCTCCCCTTAGAGAG	10529
rs138736457	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20807992	CATTTAAAAAAAAAA[A/G]AAAACCCTCTCATAT	10529
rs138745639	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21082104	CCTAACCTGAATATA[A/G]CCATGAAGAAACATC	10529
rs138756056	snp	A/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20950622	CCAATGTTTCATGAA[A/T]AAAGGTGTATACGTG	10529
rs138757991	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21020708	GTCCTCCTCTTGGGC[A/G]GCCTCCCTCCATCTT	10529
rs138763862	in-del	-/TAATATACTTAATATAACATATATAGTTATAT			intron-variant	NEBL	GRCh38.p7	10:21119419	TAAAGCAAATATTTG[lengthTooLong]TAATATACTGAATAT	10529
rs138776204	snp	G/T	0.0111196	0.0737302	intron-variant	NEBL	GRCh38.p7	10:20921036	CTGGAGTAATGACAG[G/T]AGGAACAGGGAATCA	10529
rs138776770	snp	C/T	0.0232847	0.105357	intron-variant	NEBL	GRCh38.p7	10:20953776	TTGAGAAACTAAAAA[C/T]ATCCTTGCAAAGAGG	10529
rs138777383	snp	C/T	0.0271762	0.113356	intron-variant	NEBL	GRCh38.p7	10:21011310	TATTTACGATGTACT[C/T]GTATTCTGATACAAA	10529
rs138785162	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20863345	ATGAAGGTGTTTCAC[C/T]ATAGCCACATAAACA	10529
rs138786863	snp	A/G	0.000798403	0.0199641	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21133357	GAGGCCAGGCTTAGC[A/G]GAGGGGGCTCCTTAC	10529
rs138791462	snp	G/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21055604	TTATTTAACCTCTGT[G/T]TCTCGGTTCTGTCAT	10529
rs138810324	snp	A/C	0.00119737	0.0244387	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20784012	AAATCACAGATTTTC[A/C]AAAGCATGTGCTAAC	10529
rs138823295	snp	A/G	0.0182019	0.0936463	intron-variant	NEBL	GRCh38.p7	10:21028135	AGGAGGTTGAGGCAG[A/G]AGAATTGCTTGAACC	10529
rs138829580	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21095958	TAGGTTGCAGCTTCC[C/T]AGTCAGTAAAATGAA	10529
rs138835279	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21120505	TCCAAGGGTTGATAC[A/T]TGGAGAATACTCTAT	10529
rs138842278	snp	C/G	0.00914312	0.0669923	intron-variant, downstream-variant-500B	NEBL, LOC102725112	GRCh38.p7	10:20880343	CCAGCCTGGGTGACA[C/G]AGCGAGGCTCTGTGT	10529
rs138843407	snp	C/G	0.00716266	0.059414	intron-variant	NEBL	GRCh38.p7	10:20816058	CAATCCTGAGCCACA[C/G]TGCCTGGCTCACAGT	10529
rs138845734	snp	A/C	0.0107246	0.0724382	downstream-variant-500B	NEBL	GRCh38.p7	10:20779746	TAAATTATTTTTTGT[A/C]AGAAAAAAAAAAATC	10529
rs138848631	snp	A/G	0.00478085	0.0486577	intron-variant	NEBL	GRCh38.p7	10:21159125	CCACCCTTTTTTTAA[A/G]GATGTATTCCCCCTT	10529
rs138867670	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21163392	ACAGGCCATCAAAAA[G/T]ACATCTACTTATAGG	10529
rs138868419	snp	C/T	0.00953873	0.0683987	intron-variant	NEBL	GRCh38.p7	10:21118237	TTATGTTTGTTGTTC[C/T]ATAATCCCTTCCTTA	10529
rs138871110	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21076797	CCCACTTATATTTGG[A/C]CCTAGAGTAGTCAAA	10529
rs138871736	snp	A/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20932611	TAAAATTTTTAAGAA[A/T]AGAATAAGTATTCTT	10529
rs138877807	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:20837634	ACAGATTTTTGATGC[A/T]GACAAACCAGCCTTC	10529
rs138882665	snp	A/C	0.000798403	0.0199641	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20851117	TCGGTTTATAAAATG[A/C]GTGATATTTTTTATC	10529
rs138886453	snp	C/T	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:21053136	ACAAATATTATATCA[C/T]GATAAATGAAAATAA	10529
rs138887907	snp	C/T	0.00438332	0.0466095	intron-variant	NEBL	GRCh38.p7	10:20788290	AGTAAAACTTATAGT[C/T]ATATGTGCTATAAAA	10529
rs138895473	snp	A/G/T	0.0115144	0.0749975	intron-variant	NEBL	GRCh38.p7	10:21110055	TGCTAGCTTTTGAAT[A/G/T]TGTCTGCTCCTGCTT	10529
rs138931099	snp	A/C	0.0379877	0.132479	intron-variant	NEBL	GRCh38.p7	10:21112629	AGCATTAGGAAAATA[A/C]CTAATGTAAATGACG	10529
rs138931763	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21069205	ATCATAACTATTTTC[A/G]AGTTTGCATGGAACC	10529
rs138932199	snp	C/T	1.74296e-05	0.00295204	NEBL	10	allele_origin=T(germline)/C(germline)	10:20840808	ATTAAGTTCCATTCC[C/T]TTCCCTTTTATCTCA	10529
rs138936148	snp	A/G	0.0271762	0.113356	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21137962	GGAAGGGAAGGGAAG[A/G]GAATGGAAAGGAAGA	10529
rs138940616	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20965659	TGTATGCGGAACAGC[A/G]GTATGCCCTGACTTG	10529
rs138948220	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20908933	AGATTTCAAACTTAT[G/T]TGTGCTACACTTTTT	10529
rs138957953	snp	C/G	0.00755907	0.0610114	intron-variant	NEBL	GRCh38.p7	10:20963853	GAGTGTTGCAGGATT[C/G]CTATTTCTTTTGAAT	10529
rs138971916	snp	A/G	0.00398564	0.0444627	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20879066	AAATACTGGAAACTC[A/G]GGATTTCTCTGTCAT	10529
rs138997555	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20955488	GACTCATGCAAAAGC[C/T]CAGAACAGAGTAAGT	10529
rs139005664	snp	A/G	0.000798403	0.0199641	intron-variant, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20879600	AAAACACTCTGCACA[A/G]TGGGACTATGGGGGC	10529
rs139010589	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20872380	TCCAGAATATCACTC[C/T]TTGGGAATATTCCAT	10529
rs139011034	in-del	-/AAAAAAAAACC/AAAAC			intron-variant	NEBL	GRCh38.p7	10:21036565	GATAGAAAAACAAAA[-/AAAAAAAAACC/AAAAC]CAGCCAATGATATCA	10529
rs139015833	snp	A/C/G	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21002741	AAACAACCAGATCTC[A/C/G]GGAGAACTCACTTAC	10529
rs139016784	snp	A/G	1.64836e-05	0.0028708	intron-variant, missense, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20868696	AAGCTTCCACGGCAT[A/G]TTCAAAATCTGGTCT	10529
rs139035935	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21005287	TAGAGCAATAAGTCA[C/T]AGAATACCCATCTAA	10529
rs139039342	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20905992	TTATGTGCCTTGAAC[A/G]TAATTTTTCCTTCTT	10529
rs139049256	snp	A/C	0.00557542	0.0525036	intron-variant	NEBL	GRCh38.p7	10:20931671	AGTCTCCGGCCCATG[A/C]AGGGCGCAGAAGTTA	10529
rs139051323	snp	C/T	0.0146672	0.084371	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20875908	AAATCATGTAACTGG[C/T]ATATAGTGGTAATCT	10529
rs139060367	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20936290	AGTGAATGAAACAGA[A/T]TCACTTTATTACTCT	10529
rs139060522	snp	A/G	0.0372196	0.131242	intron-variant	NEBL	GRCh38.p7	10:20900975	GTGAGCCAAGATCGC[A/G]CCACTGCACTCCAGC	10529
rs139062879	snp	C/T	0.00636936	0.0560724	intron-variant	NEBL	GRCh38.p7	10:20839363	CTAATGTAGGGTTAA[C/T]GTGATGACAATGTTA	10529
rs139079386	snp	C/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21169728	AATTCCTATTTCCCC[C/G]TATTTATCTGCTCAA	10529
rs139098744	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20903915	ATTGGGAACAATTAC[A/G]CTACTCAAGTGACAA	10529
rs139099292	snp	C/T	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21128251	TTTGAAGACCATAGA[C/T]ATTTTCTTCCTCTTG	10529
rs139101243	snp	C/T	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20843146	ACTCCCTTGATAAGA[C/T]TAATATCTCTAAAGG	10529
rs139110851	snp	C/T	0.0217236	0.101931	intron-variant	NEBL	GRCh38.p7	10:20967239	GAGAATGAATAAATC[C/T]AATGTAATATTATTT	10529
rs139114461	in-del	-/AA			intron-variant	NEBL	GRCh38.p7	10:21160877	CTTATTTCCAGGGGG[-/AA]AAAAAAAAAAAACAT	10529
rs139119803	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21065139	TATAAACATGGAAAT[G/T]GGTGTAAGGAACAAA	10529
rs139129696	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20998394	GCAAACAACTGGCTC[A/G]TCGTTAACTCCCAGT	10529
rs139134086	snp	A/T	0.000798403	0.0199641	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20882149	TCTATCCTGGGTGAT[A/T]GAGCAAGATCCTGCA	10529
rs139137124	snp	C/G	0.0158469	0.0875917	intron-variant	NEBL	GRCh38.p7	10:20818320	GGGGGCTGGGGGTGG[C/G]AGGCCAGCATGTCCT	10529
rs139146047	snp	C/G	1.65056e-05	0.00287272	intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20826488	TCACTCGTTCGATCT[C/G]TGGGCTATCTTTCAC	10529
rs139156783	snp	A/G	3.30038e-05	0.00406212	utr-variant-3-prime, synonymous-codon, nc-transcript-variant	NEBL	GRCh38.p7	10:20785813	TCTCTGCACTGTGCC[A/G]TACATCCAGCCATCG	10529
rs139165271	snp	G/T	0.00755907	0.0610114	intron-variant	NEBL	GRCh38.p7	10:21101984	AAGGTAGACAGGGCA[G/T]GCCTGTCTTCCATAA	10529
rs139174571	snp	A/G	0.00835141	0.0640778	intron-variant	NEBL	GRCh38.p7	10:21033302	CACAAGAAGGATCAC[A/G]TTCGATTCCTTTGAT	10529
rs139177766	snp	A/G	0.00398564	0.0444627	intron-variant, utr-variant-5-prime	NEBL	GRCh38.p7	10:20958031	GAATGTCTGGCGATG[A/G]TTGTGCTTTGAGATC	10529
rs139181160	snp	C/T	0.0376037	0.131863	intron-variant	NEBL	GRCh38.p7	10:21105587	AATCCAGTCTATCAT[C/T]GATGGACATTTGGGT	10529
rs139189309	snp	A/G	0.0119091	0.0762411	intron-variant	NEBL	GRCh38.p7	10:21011930	ATCGCCTTCCACACT[A/G]TGGGAGAGACTAAGA	10529
rs139196145	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20993832	ACAATTACAGAGGCA[C/T]CTACTCCCTGATCTG	10529
rs139196791	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:20828081	CTTAAAATAAAAGTT[-/A]AAAAAAAAAAGTGCT	10529
rs139211769	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21001545	AAAGCTCAATTTTCA[A/G]TAATTAGGAGGTAAC	10529
rs139212886	snp	C/T	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20996194	AATGTGCCACTACGA[C/T]GTGATACGCTTTCAA	10529
rs139225439	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20829037	TGTAATGGGTATTGT[C/T]CTAAATACTTAACAC	10529
rs139230777	snp	A/G	0.0244538	0.107838	intron-variant	NEBL	GRCh38.p7	10:20934108	TGATTGCAAGTTCTC[A/G]CTCCCTGCTTCAGAC	10529
rs139279276	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20860972	CTGTTCTGGTTCCAT[A/T]TGATAATAAAAAATT	10529
rs139286511	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21104432	TTTGTAGTTTCCAGT[C/G]TAGAAGTTTTACACA	10529
rs139290132	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20797188	TACTACTGTCCATGT[C/T]GTATAAATCAATATT	10529
rs139294325	snp	A/G	0.0115144	0.0749975	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21135534	GTGACGCTGCCAACA[A/G]TCAGCCTCCTGCAAC	10529
rs139294499	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21017794	TGGCACAAAGCACTA[C/T]GGAGTCCAATCCACA	10529
rs139297826	snp	A/C	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21041175	GTAATCAGCATAATA[A/C]CTGATAGTTTTTCAG	10529
rs139300057	snp	C/G	0.046775	0.145601	intron-variant	NEBL	GRCh38.p7	10:20820783	TGAACTGAGATCACG[C/G]CACTGCACTCCAGCC	10529
rs139316596	snp	C/T	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:21164331	TCGAGGACAAGGGTG[C/T]CATGCATGGCTATGT	10529
rs139317871	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21069385	CATGTCACATAAACC[A/C]CAGCCAGTAGAGCAC	10529
rs139320127	snp	A/G	0.0341408	0.126114	intron-variant	NEBL	GRCh38.p7	10:20918776	GAATGGTGTAAACCC[A/G]GGAGGTAGAGCTTGC	10529
rs139328392	snp	A/T	0.00119737	0.0244387	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20861938	CCAAACATCACAGCT[A/T]CGCCTGGCCTACCTT	10529
rs139331136	snp	C/T	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:21097833	TGAAGACATTGGACT[C/T]TTTTATGGATGTAAT	10529
rs139335971	snp	A/G	0.00835141	0.0640778	intron-variant	NEBL	GRCh38.p7	10:21098860	CTAGCCAGGCATGGC[A/G]GCTCACACCTGTAAT	10529
rs139338531	snp	A/G	1.69519e-05	0.0029113	utr-variant-3-prime, synonymous-codon, nc-transcript-variant	NEBL	GRCh38.p7	10:20785756	AAATAATTAATTAAC[A/G]AACTCAATGTAATTC	10529
rs139346039	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21031179	AAGGAAACAGCATGT[C/G]ACTAGGGTGGAGGCA	10529
rs139356765	snp	C/G	0.00835141	0.0640778	intron-variant	NEBL	GRCh38.p7	10:21168173	GAGAATATAAACAAG[C/G]AACATATTTAAACTG	10529
rs139358259	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20793267	TAAAGACATGCCTAA[A/T]CATCGTGATACAAAA	10529
rs139362605	snp	A/G	0.00755907	0.0610114	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20872746	AACCAAGATGGCGAC[A/G]AGAGTGACCTCTGGT	10529
rs139366954	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20806683	AGCCCCTTACAGCGG[A/G]TGCATGTTTCTTTTG	10529
rs139372665	snp	A/G	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:21100524	GCCGTCCAGTTTCCC[A/G]TGAACCCTGGGGGGC	10529
rs139375311	snp	G/T	1.70799e-05	0.00292227	utr-variant-5-prime, intron-variant	C10orf113, NEBL	GRCh38.p7	10:21146542	GAAAATGGTGAAAAT[G/T]GTGCTGTGTTTGGGC	10529
rs139378482	snp	A/G	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:21053633	AATAATCCCCAAGAA[A/G]TTATGAAAATCAAGG	10529
rs139407188	snp	A/G	0.00557542	0.0525036	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20897793	AAAAATACCCACTTT[A/G]TATTAGCTGATTAGA	10529
rs139408605	snp	C/G	0.0115144	0.0749975	intron-variant	NEBL	GRCh38.p7	10:20944354	GCACTGAGCCAAGAT[C/G]ACGTGACTGCACTCC	10529
rs139440501	snp	A/G	0.00517822	0.0506191	intron-variant	NEBL	GRCh38.p7	10:20990939	CTTTCTTCCTGCCCC[A/G]CTACTCAGTCCACAA	10529
rs139449262	snp	C/G/T	0.0091479	0.0670627	intron-variant	NEBL	GRCh38.p7	10:20906829	AATCTCTCCAGTCAA[C/G/T]GAACAAAACCAACAA	10529
rs139450033	snp	C/T	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:21157013	TCCTACAAGCAAGAA[C/T]AATCTATCAGAGAAC	10529
rs139452780	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20849140	TAAGAACCCAGCTGC[A/G]CCCACAAAACTTTGA	10529
rs139456681	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21165190	GGTGGGAATTATTTT[C/T]CCATTGTACAGATTA	10529
rs139464132	snp	A/G	0.00716266	0.059414	intron-variant	NEBL	GRCh38.p7	10:20979156	GGCACGGTGGCTCAC[A/G]CCTGTTATCCCAACA	10529
rs139469852	snp	G/T	0.00755907	0.0610114	intron-variant	NEBL	GRCh38.p7	10:20809504	AAACAAACCTCCTTT[G/T]GTCTCAGCACTTTAG	10529
rs139481324	snp	A/T	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:21153682	CACCACAACCAGCTA[A/T]TTTTTGTATTTTCAG	10529
rs139491846	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21160628	AGAGAGAAAGAGAAA[C/T]GGAGAGATAGTGGGG	10529
rs139503167	snp	A/G	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:21093446	TCAAGGGAACCAGAC[A/G]CCCAAAGCCAAGTTC	10529
rs139532800	snp	A/C			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20855526	AAAACAAAACAAAAC[A/C]AAAAAAAAACGAAGG	10529
rs139553985	snp	C/T	0.00557542	0.0525036	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20853453	AAAATGTGGCACATA[C/T]ACACAACGGAATACT	10529
rs139559775	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20790773	AGGTAAATAAAACAA[A/G]CAAAAGGAAATCTAA	10529
rs139567419	snp	G/T	0.00438332	0.0466095	intron-variant	NEBL	GRCh38.p7	10:21088857	TCCAAGCTTCAGGGT[G/T]AAGGGAAGTCTTTCT	10529
rs139581346	snp	C/T	0.000115707	0.00760528	intron-variant, splice-donor-variant	NEBL	GRCh38.p7	10:20889844	GCTTTTGATACCTTA[C/T]CTCAGAAATAAAAGC	10529
rs139591701	snp	A/G	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20996669	CACTAGTTCTCAGGG[A/G]GCTAGACTGTAATGT	10529
rs139603518	snp	A/C	0.00914312	0.0669923	intron-variant	NEBL	GRCh38.p7	10:21082627	GGGCTATTTCCTCAC[A/C]TAATTCCGATGCCCA	10529
rs139608088	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20852683	AAATCAACTTAGAAT[C/T]AAAGAGACTGATTAG	10529
rs139609418	snp	C/G			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21139437	TCCACTCAAATCAGA[C/G]GAAAGAAGAACATAA	10529
rs139610204	snp	C/T	0.000276582	0.0117565	intron-variant, missense, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20852645	AAGAGCTTTTTATAT[C/T]CTCGCTAAAATACAG	10529
rs139611319	snp	G/T	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:21044931	TACTAAAAGACTGAT[G/T]AACTGAAAGAATGAT	10529
rs139620622	snp	A/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20975666	CCTACAGTCATTACA[A/T]AACTTTACAAAACAA	10529
rs139625541	snp	G/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21102597	GCAGTTGTCTTACTG[G/T]CATGCTTGACATTTC	10529
rs139632891	snp	C/G	0.0111196	0.0737302	intron-variant	NEBL	GRCh38.p7	10:20976141	GGAGTTCAAGACCAG[C/G]CTAGCCAACATGGTG	10529
rs139650432	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20885877	ACAGTCACCCATGCA[A/G]AACGTTGACATCATA	10529
rs139670621	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20842951	TCCACATAAAAGTGA[C/G]AATATGCAGGATTTG	10529
rs139675939	snp	C/G	0.00478085	0.0486577	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20849439	CAACGCAACACTGTT[C/G]GGGGGTGGGAACTCT	10529
rs139681077	snp	A/G	0.00318978	0.0398085	downstream-variant-500B	NEBL	GRCh38.p7	10:20779864	GTAGTGAATTCTTCA[A/G]ATAAATAACTGTGCT	10529
rs139730450	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21078104	GATGGAAATGCATTC[C/T]ATGGGGGATCGAAAA	10529
rs139739131	snp	C/T	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:21075608	TGAGAGGTTGGCCAC[C/T]GGTCTGCAGCGTGGA	10529
rs139744509	snp	G/T	0.000906163	0.0212664	missense, intron-variant, utr-variant-3-prime	C10orf113, NEBL	GRCh38.p7	10:21125989	GCTGCCTGGATGGGC[G/T]GCTTGTAGAGACTGA	10529
rs139748260	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21077315	GTACATTTTAAATTG[A/C]TTTTGCTGGCCGGGC	10529
rs139752215	snp	C/T	0.00755907	0.0610114	intron-variant	NEBL	GRCh38.p7	10:21036286	TAGCAAGACCTCCTT[C/T]CTACAAAAAATTCTC	10529
rs139763712	snp	C/T	0.00993419	0.0697739	intron-variant	NEBL	GRCh38.p7	10:21115386	TTCCATCTGGTATCA[C/T]TTTCTTTCTGTCTAA	10529
rs139772258	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20921864	ATCCATACATCCACA[C/T]ACTCACATTCATATA	10529
rs139784284	snp	C/T	0.00716266	0.059414	intron-variant	NEBL	GRCh38.p7	10:20839154	CTTATTCTCCTAGGC[C/T]GGTTCTTCCTTCTCC	10529
rs139785336	snp	C/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20972180	AACTAACACAAAACA[C/G]TCATGAAAGTGAAAA	10529
rs139787423	snp	C/T	0.0733688	0.176922	intron-variant	NEBL	GRCh38.p7	10:21039445	GTTTCTGCATATGGC[C/T]AGCCAGTTTTCCCAG	10529
rs139791007	snp	A/T	0.0150606	0.0854603	intron-variant	NEBL	GRCh38.p7	10:20928787	CTCCTACTCTACCAG[A/T]CCAATTCCATCAACG	10529
rs139791706	snp	C/G	0.00557542	0.0525036	intron-variant	NEBL	GRCh38.p7	10:21033233	GTATCTAAGATATGA[C/G]TATACTCTGAAAAAT	10529
rs139798051	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20874629	GCCTGAAGATAGCTT[A/G]GATTTGTCAATTACA	10529
rs139809958	snp	A/C/T	0.00042859	0.0146333	intron-variant, missense, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20880891	GCAGCATCATGTTTC[A/C/T]GCTTGTAGGCCACCT	10529
rs139818399	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20877181	GCAACTTTTAAGATG[C/G]AGGCTCTGCTGTGAA	10529
rs139819724	snp	C/T	0.000117346	0.00765894	missense, intron-variant	C10orf113, NEBL	GRCh38.p7	10:21146367	CTGGAATGTACATTT[C/T]AGCCACACAAGAAAA	10529
rs139838222	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21021340	TGCAAATCTGATCAC[A/G]TCACTCCCCTGAGTA	10529
rs139850282	snp	A/G	0.00517822	0.0506191	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21134327	TCTCCTAGACTCAAA[A/G]CTGCTTTATAAAGAC	10529
rs139852813	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20800638	TTTCTAATAGGTTTT[C/T]CTGGTTATCTAATTT	10529
rs139856456	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21026764	CATTCATTTGAAAGG[C/T]CTGCTTAGAAGGATG	10529
rs139864931	snp	C/T	0.000798403	0.0199641	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21139710	ACCCAACTCCCATTA[C/T]AGACCTGCTTTCCAC	10529
rs139876568	snp	G/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20959306	TAATTTTCAGGATTA[G/T]AATTTCCCAGCATCT	10529
rs139882736	in-del	-/CA			intron-variant	NEBL	GRCh38.p7	10:21046008	ATGTGGTACACACAC[-/CA]ACACACACACGTGTG	10529
rs139887121	snp	A/G	1.65132e-05	0.00287339	intron-variant, splice-donor-variant	NEBL	GRCh38.p7	10:20808508	CAGTGAATGTTTGAT[A/G]CCTCCTTCATCAGAC	10529
rs139900114	snp	G/T	0.00914312	0.0669923	intron-variant	NEBL	GRCh38.p7	10:20838585	GCAATGGGTTTGAGA[G/T]GTTGGTCTCTAATCT	10529
rs139903100	snp	A/G	0.0197687	0.0974348	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21142779	TGCTATGAACTGCGC[A/G]TGTGAGGGATCCCAG	10529
rs139909124	snp	A/G	0.0107246	0.0724382	intron-variant	NEBL	GRCh38.p7	10:20825778	AAAAACAATTTATCC[A/G]TAATATTAAGCACCT	10529
rs139914727	snp	A/C	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21170094	GAACTAAGCAATAAG[A/C]ACTAAATAATTTTCA	10529
rs139932630	snp	G/T	0.00874735	0.0655527	intron-variant	NEBL	GRCh38.p7	10:21086956	CAATCCCAATCAATT[G/T]GGTTGTCTGCTCAAC	10529
rs139933937	snp	G/T	0.00478085	0.0486577	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21128901	GTTTAAGGCTGTCAG[G/T]GGGCTAAGTAAGAGC	10529
rs139936796	snp	C/T	0.0209421	0.100162	intron-variant, upstream-variant-2KB	NEBL, NEBL-AS1	GRCh38.p7	10:21173087	TCAGTCACTCCGGAT[C/T]GCTCCTGGGTGTCTC	10529
rs139942900	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21063193	CTCTTAACCCCATGC[A/G]CACGCAGTTCCGATC	10529
rs139969365	snp	A/G	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:20918197	AACCCTGTCGCTACT[A/G]AAATACAAAAATTAG	10529
rs139979367	in-del	-/ATATATAGATATATAGAGACTATAG			intron-variant	NEBL	GRCh38.p7	10:20822653	TATCTAATATAGGCT[-/ATATATAGATATATAGAGACTATAG]ATATATAGATATATA	10529
rs139986505	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20925686	CTAAGTTGAACTCAT[C/T]ATTGGAATTCCAGAG	10529
rs139995138	snp	G/T	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20822414	AAATATATATATTCA[G/T]AGATATCTATACCTA	10529
rs140003979	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21016763	AGATATCAAAACTCT[A/G]AGGAAATGCTCTCAT	10529
rs140005186	in-del	-/CTT			intron-variant	NEBL	GRCh38.p7	10:21016933	AAGAAACCATAATGA[-/CTT]CTTCCTACTTATACT	10529
rs140007865	snp	C/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20914134	GAGAGGAAACACACT[C/G]GTCATTTGGTGACCA	10529
rs140008008	snp	C/G	0.0232847	0.105357	intron-variant	NEBL	GRCh38.p7	10:20948079	GCATGTGGCCCAAGG[C/G]CCATGGGTTGGACAA	10529
rs140011102	snp	G/T	0.0107246	0.0724382	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20857583	ATGTGTCTTAGGGCT[G/T]TCAGTTACGAGAGCT	10529
rs140022920	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20895901	TTCAGCATTTATATG[C/T]ATTACCATTATTTAA	10529
rs140030639	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20861476	GAGCCACCGCGCCCA[A/G]CCACAGTCTTATTGC	10529
rs140030947	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20798237	AGGGCCACAGATAAC[A/G]GGCAAGCAAAATGCA	10529
rs140043013	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20984248	TTTCCACCATCATTG[C/T]AAAACAAACTATCGT	10529
rs140051010	snp	C/T	0.0205511	0.0992634	intron-variant	NEBL	GRCh38.p7	10:20925191	ATACTCAAACATATA[C/T]ATGCATATATGCATG	10529
rs140059333	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21115070	TATCTCTTTATATTG[C/T]TTCTTTAGGCATTTC	10529
rs140071169	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21049917	CAACGGGCTAGAAAA[A/G]TGGTCTCTCCAGAAT	10529
rs140078169	snp	A/G/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21113130	GAAGTGGAGGAGGAG[A/G/T]GAAGAGGAGGAGGAG	10529
rs140087097	snp	G/T	0.0103295	0.0711199	intron-variant	NEBL	GRCh38.p7	10:20892778	AGGCTGAAATCGGAT[G/T]ACAGACATGGAGATG	10529
rs140087459	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20927333	ATCTTTTCTTCACAA[A/G]GATTCTTTATGAAAT	10529
rs140088913	snp	A/G	0.00835141	0.0640778	intron-variant	NEBL	GRCh38.p7	10:21012726	ACTATATATTGAAAC[A/G]CCTAATACAAGGGCC	10529
rs140094146	snp	A/G	0.00755907	0.0610114	intron-variant	NEBL	GRCh38.p7	10:20944593	GGCATACATATTTAT[A/G]TGGGTTTGCACTCTC	10529
rs140099841	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20870216	CTGTAATCCCAGCTA[C/T]TCGGGAGGCTGAGGA	10529
rs140118858	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20877069	TATAAATTGAACTTC[A/C]TTTACTTGTTTCAAA	10529
rs140122816	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20809191	GACATAGCTATCTAT[C/T]GTTTAACATAACTGC	10529
rs140125935	snp	A/C	0.0107246	0.0724382	intron-variant	NEBL	GRCh38.p7	10:21152317	CAGTGTAATATTTTA[A/C]ATCCGTTAGTCCCAA	10529
rs140127572	snp	A/G	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:21115610	TCCAACAAGGAGTTC[A/G]CTCAATATCACCTTT	10529
rs140154452	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21047079	TGAATGTTACTGCCA[C/T]GCAGACTTTCCAGAT	10529
rs140175793	snp	C/T	0.00438332	0.0466095	intron-variant	NEBL	GRCh38.p7	10:21021834	CTATATCGCTAGCAC[C/T]TGCTAGTGTCTGCCT	10529
rs140182569	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20950064	CAGCATTTCCCTCTA[C/T]CTGGCATTTCTCCCA	10529
rs140192833	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20874888	GGGATTACAGGTGAA[C/T]ACCACCACACCCAGA	10529
rs140206774	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20806880	ACATCAATTCCAGTA[G/T]GCTGAACTGAGTAAC	10529
rs140216100	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20981132	TCACTAAAATTCCAC[C/T]TAAACACACAGGTTA	10529
rs140216107	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21025750	CATCTGTGTGCCTTT[A/G]GGTTAGGTTTCTTAA	10529
rs140220019	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20802209	ACACAAAGTAATACC[A/G]GGAAGCAGATACACA	10529
rs140221408	snp	C/T	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:20919916	GGTAGCAGGGGGAAA[C/T]TGCATCATGAAGGGC	10529
rs140221620	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20863057	TTTTTAAAGAATTAT[A/G]AGAGACAGCAGGATT	10529
rs140240431	snp	C/T	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:20804727	CAGAAATGGTGAGAG[C/T]GGACAGATATACTTG	10529
rs140241442	snp	C/T	0.000798403	0.0199641	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21144156	GGGGCTGTCACTCTA[C/T]TCCTCCTTTGTCTTT	10529
rs140245727	snp	A/G	0.000824973	0.020293	intron-variant, synonymous-codon, nc-transcript-variant	NEBL	GRCh38.p7	10:20808586	GATTTCTGACCTGTC[A/G]TCTCCGAGACCTGTA	10529
rs140249442	snp	A/T	0.0154538	0.0865337	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20959886	ATACTGCTGTCTATA[A/T]AACATATTATATATG	10529
rs140276042	snp	C/T	0.0228947	0.104514	intron-variant	NEBL	GRCh38.p7	10:20991740	TAGTACCCAATACTT[C/T]GTCAACCTTTGCTCC	10529
rs140281057	snp	A/G			utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20785039	AATTTGCCCTTTGCA[A/G]AGTAGCTGTGAAGTT	10529
rs140282211	snp	C/T	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:20894306	GAGACTCCATCTCTA[C/T]GAAAAAGAAAATGAA	10529
rs140282617	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20930354	TCATCTTCTTTTCTC[C/T]ATTTCTATGGCCACC	10529
rs140284605	snp	A/G	0.0146672	0.084371	intron-variant	NEBL	GRCh38.p7	10:21119240	ACTACCTCATCTCTA[A/G]CACAAAGTTCTTTCT	10529
rs140295266	snp	C/T	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:21162654	GGCTGAGAATATCTA[C/T]GGTCCAATTTCAGCA	10529
rs140302928	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20898514	CTACACAGTCATCAC[A/G]TATAAATTATTTCTG	10529
rs140305246	snp	A/G	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20807748	TTCTCATATGCTTCA[A/G]TCCTTTCCCCCTCCT	10529
rs140310759	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21060422	GTGGTTCTCAAACTT[A/G]AGCGTGTATCAGAAT	10529
rs140312871	in-del	-/A	0.0209421	0.100162	intron-variant	NEBL	GRCh38.p7	10:21055319	AGAGACATTGTAAAG[-/A]GGGAAATATTCAGCT	10529
rs140320137	snp	G/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20789250	TACTTGAATCTATTT[G/T]TAAAGTTTGAAAGAT	10529
rs140322323	snp	A/T	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:21123697	ATAGTTCCCCTTCTC[A/T]GAATTCTGATGATCA	10529
rs140327544	snp	A/C	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:21054310	CAAAAAGTGCCAGTT[A/C]AGGTAGAGCCAGGCC	10529
rs140337024	snp	C/T	0.00835141	0.0640778	intron-variant	NEBL	GRCh38.p7	10:21094704	AGAAGACCAGAAGTC[C/T]GCTCCTTTGTAAATG	10529
rs140337415	snp	C/T	0.00676609	0.0577691	intron-variant	NEBL	GRCh38.p7	10:21119330	TGAAGATACCCTTCA[C/T]CTAGATTCACCAATC	10529
rs140343003	snp	C/T	0.00716266	0.059414	intron-variant	NEBL	GRCh38.p7	10:20833018	GGCACTGATAACAGA[C/T]AGCCACCAAGGTCTG	10529
rs140348868	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21161623	TAATTAGTGACCCCC[C/T]ACCCCCTGTTCCTGT	10529
rs140356778	in-del	-/TTAAAAAAAAAAAAAAAAAAAAAAAA			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21138820	ACCAAACTAAACTAT[-/TTAAAAAAAAAAAAAAAAAAAAAAAA]TTAAAAAAAAAAAAA	10529
rs140362065	snp	A/G	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:20987096	TAAAAATATTAATGT[A/G]TTTTTCTAAGCTATT	10529
rs140369252	snp	C/T	0.00398564	0.0444627	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21130643	CTAAATAACACATGG[C/T]TCAAAGAATAAATCT	10529
rs140407263	snp	C/T	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:21027234	GACCCCAGCACAGGC[C/T]CCTTTGTGCGTAACA	10529
rs140425168	snp	A/G	0.00993419	0.0697739	intron-variant	NEBL	GRCh38.p7	10:20907984	GACATTTTTTGGGAA[A/G]GAGGAACTCCATATA	10529
rs140427634	snp	C/T	0.0111196	0.0737302	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20850323	TCCAGACCCACTGAA[C/T]ATTCTGCGTCCTTTC	10529
rs140434508	snp	C/T	0.0162398	0.0886349	intron-variant	NEBL	GRCh38.p7	10:21166963	AATTTAATTTCCTTC[C/T]GTGTCCTCTGATTAC	10529
rs140434528	snp	C/T	0.0154538	0.0865337	intron-variant	NEBL	GRCh38.p7	10:20822958	TACCTTTTGGAGTCT[C/T]CAATGTCTATGATTC	10529
rs140440030	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21099295	TAACCTCACACACTG[A/C]GTAGCCCACCCACCG	10529
rs140445401	snp	A/G	0.00716266	0.059414	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20881646	TTAATTACTTTGTTT[A/G]GTTTATGTATAATTA	10529
rs140454659	in-del	-/CAC			intron-variant	NEBL	GRCh38.p7	10:21015037	TGCCCTCATAAATTA[-/CAC]CACATACTCCATTTA	10529
rs140455213	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20967867	TGATCAACTATCTCA[C/T]GATAAGAATATTTTC	10529
rs140458822	snp	C/G	0.00438332	0.0466095	intron-variant	NEBL	GRCh38.p7	10:21060462	TGCTTGTTAAACCAG[C/G]CTTATTCTGCACAGC	10529
rs140468030	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20911033	ACTGGCTGTAGTGTT[A/G]TGAGCTTGTAGTTCC	10529
rs140471684	snp	C/G	0.0221141	0.102801	intron-variant	NEBL	GRCh38.p7	10:20993002	GTTAGCCAGGATGGT[C/G]TTGATCTCCTGACCT	10529
rs140484376	snp	C/G	0.00716266	0.059414	intron-variant	NEBL	GRCh38.p7	10:20787475	GTGATCTCTAGATTA[C/G]TAGAAATCTTAGTAA	10529
rs140507662	snp	A/T	0.0107246	0.0724382	intron-variant, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20880064	CTGTTCTTACAAACA[A/T]CCTAAAAGAAACAAT	10529
rs140509078	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21004443	AGAATCACCTGGGCC[A/G]GGCACGGTGGCTCAC	10529
rs140510061	snp	A/T	0.00557542	0.0525036	intron-variant	NEBL	GRCh38.p7	10:20913080	AATTGTTTTGAACAG[A/T]GGGTGAAATAGGCTT	10529
rs140510183	snp	C/T	0.116488	0.211364	intron-variant	NEBL	GRCh38.p7	10:20938384	CCTGAGGGTCCTGAC[C/T]GTTAGAAGGAAAACT	10529
rs140515621	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20814905	AGAAATGTCACTAGG[A/G]AGCTGTAAATTGCAA	10529
rs140526764	snp	C/G/T	1.64795e-05	0.00287045	missense, intron-variant, utr-variant-3-prime	C10orf113, NEBL	GRCh38.p7	10:21125965	CAGTTGCCTGGATCT[C/G/T]GTTCAGGAGCTGCCT	10529
rs140530772	snp	A/C	0.000247209	0.011115	stop-gained, intron-variant	C10orf113, NEBL	GRCh38.p7	10:21146418	AAGCACAAACACTCT[A/C]TCTCATATAAGCTAG	10529
rs140534422	snp	A/T	0.00119737	0.0244387	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20855299	ATAATACAGACTTTA[A/T]AATTTGATTAGAAGT	10529
rs140536533	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20791752	GGAAATATACGTAAA[C/T]ACACAAAGATTAGAG	10529
rs140549583	snp	A/G	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:21104680	TCTGTGAATGAAGGT[A/G]GTTGTATCCTTCTTT	10529
rs140576250	snp	G/T	0.067446	0.170804	intron-variant	NEBL	GRCh38.p7	10:21072099	CTGGGATTACAGGTA[G/T]GAGCCACCGTGCCTG	10529
rs140587357	snp	A/C	0.00914312	0.0669923	intron-variant	NEBL	GRCh38.p7	10:21047418	AATACATGTGGGGTT[A/C]TGCAATGCTTTAGTT	10529
rs140591320	snp	G/T	0.031825	0.122064	intron-variant	NEBL	GRCh38.p7	10:20973817	TAAAACTCTAAGACA[G/T]CAAACTTTAGAACTA	10529
rs140591364	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20977346	CCCATTTCTTAACCA[A/G]TGTTTGACTTGTCAA	10529
rs140603405	snp	A/G	0.00953873	0.0683987	intron-variant	NEBL	GRCh38.p7	10:20914881	TTTGTTTTTTGAGGC[A/G]GAGTCTCACTCTGTC	10529
rs140605195	snp	A/G	0.00159617	0.0282053	intron-variant, downstream-variant-500B	NEBL, LOC102725112	GRCh38.p7	10:20880427	AATGATCCTTCTGTG[A/G]GCCATTGATTCCTGA	10529
rs140610212	snp	A/G	0.0138799	0.0821421	intron-variant	NEBL	GRCh38.p7	10:21034758	TGGTTTTTCAGGATC[A/G]ATGCACTGAGGGAGG	10529
rs140615039	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21074749	TCCCAAAGTGCTGGG[A/G]TTATAGGCGTGAGCC	10529
rs140623559	snp	C/T	0.00438332	0.0466095	intron-variant	NEBL	GRCh38.p7	10:21007781	CATCTGTGCTTGTTA[C/T]ATAGTAGAATGAGTG	10529
rs140623942	snp	A/G	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20964943	ACATAACCAGCCCCC[A/G]TGTCCATGTGTTGTA	10529
rs140633038	snp	C/T	6.75504e-05	0.00581125	intron-variant	NEBL	GRCh38.p7	10:20888052	GCTTTTTTCCAGTTA[C/T]ATGTTTTATCTACAA	10529
rs140635118	snp	C/T	0.0287284	0.116357	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20866381	GTAAATTTTATGTTA[C/T]ATAAATCTTATCACG	10529
rs140636680	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:21119475	GAATATAACATATAT[-/A]GTTATATTAATATAC	10529
rs140638478	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20911783	CAGTGGGAAATTAAA[C/T]TCTGATAGAGCCAAG	10529
rs140651137	snp	C/T	0.0174175	0.0916809	intron-variant	NEBL	GRCh38.p7	10:20802016	TGCATCTGTTTTTCA[C/T]TCCCCATCACACTCC	10529
rs140664314	snp	A/G	0.00517822	0.0506191	intron-variant	NEBL	GRCh38.p7	10:20816122	TAGGAAACTACAAAA[A/G]ATATTTTCAGAGGTT	10529
rs140685798	snp	A/T	0.00953873	0.0683987	intron-variant	NEBL	GRCh38.p7	10:20969115	CAGAAAATTGATTAA[A/T]CTCACAATGTTAGAC	10529
rs140699108	snp	C/T	0.0189856	0.0955633	intron-variant	NEBL	GRCh38.p7	10:21005626	GTGATCCCCGCTACT[C/T]GGGAGGCTCAGGTGG	10529
rs140703047	snp	G/T	0.0329836	0.124112	intron-variant	NEBL	GRCh38.p7	10:21111279	AAAAAAGAGCCCACA[G/T]AGCCAAGATAATCCT	10529
rs140703715	snp	C/G	0.0221141	0.102801	intron-variant	NEBL	GRCh38.p7	10:21105699	TCCTTTGGGTATATA[C/G]CCAATAAGGGGATCA	10529
rs140707301	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	NEBL	GRCh38.p7	10:21175424	GAAGCGAACACATTC[C/T]GTTGCTAGCGCACAG	10529
rs140720151	snp	A/T	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:21010186	TCCTCTGTATAAGGG[A/T]TCACAGAGACATGCT	10529
rs140734883	snp	A/G	0.00388112	0.0438805	intron-variant, synonymous-codon, nc-transcript-variant	NEBL	GRCh38.p7	10:20897002	CCAATTCCATGCTTA[A/G]GTCTTCAATAACAGG	10529
rs140738452	snp	G/T	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:21083270	TAAGCAATAGTCGAT[G/T]TAAATTGATTTCACA	10529
rs140752249	in-del	-/AA	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:21082155	ACTTAACTGGGCTTC[-/AA]AAGAGTCGTGAAAGT	10529
rs140766708	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20803423	AAAGAAAAATCAATC[C/T]TTAAAATAGTCCATT	10529
rs140768280	snp	A/T	0.0387552	0.1337	intron-variant	NEBL	GRCh38.p7	10:20923453	GGAGGCTGAGGTGGG[A/T]GGATCACGAGGTCAG	10529
rs140769354	snp	G/T	0.00795532	0.062565	intron-variant	NEBL	GRCh38.p7	10:20981826	AGACATGAATTGAGA[G/T]ATAGAAATAAACAGC	10529
rs140787973	snp	A/C	0.0107246	0.0724382	intron-variant	NEBL	GRCh38.p7	10:20892057	CATGTCTACATCTTA[A/C]AATTTCGGGTTGACA	10529
rs140799071	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20805573	GAGTCAACTTTTTGG[C/T]CAGGCACAGTGGCTC	10529
rs140803920	snp	C/T	8.3082e-05	0.0064447	intron-variant, synonymous-codon, nc-transcript-variant	NEBL	GRCh38.p7	10:20808652	TCGCCTATAGTGACT[C/T]GCCTTTTCTATATTG	10529
rs140808343	snp	C/G	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20934365	TGTGCTTTTTGATCA[C/G]AGAGTGTGCCACAGG	10529
rs140810972	snp	A/G	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:20836262	GAGTCTTGCTCTCTC[A/G]CGCAGGCTGGAGTGC	10529
rs140824289	snp	A/G	0.0126979	0.078662	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21125411	TGTTTTAAATTGGGG[A/G]TTGGGGAGAAGAAAT	10529
rs140830231	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20839722	TCAGCACATTCTACT[C/T]CCCCAATCCCAGACA	10529
rs140844428	snp	C/T	0.0115144	0.0749975	intron-variant	NEBL	GRCh38.p7	10:21090468	GTATACAGGAGGATG[C/T]GTGTAGGTTATATGA	10529
rs140855772	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21022785	TATGCTTGTATAACC[A/G]CTGGACTGTCAAGAG	10529
rs140861015	in-del	-/T	0.0626037	0.165477	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20783175	TGTTCAGGCATGTCA[-/T]TTTTTTTTTAAATGA	10529
rs140877887	snp	C/T	0.0158469	0.0875917	intron-variant	NEBL	GRCh38.p7	10:20951869	AAAGTTCTAAATCTG[C/T]ATCATGCACTGGAAA	10529
rs140883897	snp	C/T	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20896779	GCTCTAGCAGAAATT[C/T]TCTGTATAGGTGACC	10529
rs140885123	snp	A/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20955886	ATCTTCACAGATTGT[A/T]CACTGAATCCCTCAT	10529
rs140888177	in-del	-/AT	0.361053	0.22398	intron-variant	NEBL	GRCh38.p7	10:21123725	TCATATATCATCAGA[-/AT]ATATATATATATATC	10529
rs140902800	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20867332	TCGGGACTTATTTTA[C/T]GCTCTTCAATCAGAC	10529
rs140909841	snp	C/T	0.0244538	0.107838	intron-variant	NEBL	GRCh38.p7	10:20936797	CAAATGACCTGGTAA[C/T]CCAACACTGTTCAAC	10529
rs140924561	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20865230	ATGTAGAACAGAAAA[C/T]TATTTTGAATACCTA	10529
rs140925070	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20793599	GGCTCTGTCACCCAG[A/G]CTGGAGTGCAGTGAT	10529
rs140925541	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20926025	TGCCACCAGTAAATT[C/G]AGAAAGAGCAGAAAA	10529
rs140933195	snp	C/T			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21131836	GCTGGGTCCCAGTGC[C/T]CTTGGGTGCCCAAAG	10529
rs140935007	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20801810	AAGCATCTCTTGCAA[A/C]TCTTGAATACGTATT	10529
rs140937723	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20845934	CCATCTATGGTGTTT[C/G]ATATGAATGAAGTTG	10529
rs140941809	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20782645	GTGCTTGTGGAAACT[A/G]TGCTTACAAATGCCT	10529
rs140942012	snp	A/C	0.00279162	0.0372561	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20870641	TTCAACTACACACTT[A/C]TCTCCCTTCAAATGT	10529
rs140943705	snp	A/G	4.94499e-05	0.00497217	intron-variant, synonymous-codon, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20868691	TTTAGAAGCTTCCAC[A/G]GCATGTTCAAAATCT	10529
rs140960995	snp	C/T	0.00557542	0.0525036	intron-variant	NEBL	GRCh38.p7	10:21027790	ATTTTACCCAATGAC[C/T]AAGACCATAACTAAC	10529
rs140962045	snp	C/T	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:20957647	ACATACACAGATATA[C/T]GCACACACAGACAAG	10529
rs140967244	snp	A/C	0.00795532	0.062565	intron-variant	NEBL	GRCh38.p7	10:21170766	ATTAAACAGTCTTCA[A/C]CAGATAAAATTTTTT	10529
rs140991490	snp	C/T	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:21037043	TGACACCCCTGGCCA[C/T]GCACAGCACTTGTAG	10529
rs140995058	snp	C/T	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:21064730	AACTGTAGATGTCCA[C/T]AATTAGAAATGCAAT	10529
rs141001026	snp	A/T	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:20985162	GTACTTGAATTATCC[A/T]GAAACCATCCTGTGC	10529
rs141006909	snp	A/G	0.0126979	0.078662	intron-variant	NEBL	GRCh38.p7	10:21053804	TTGGGAGGCCGAGGC[A/G]GGTGGATCACTTGAG	10529
rs141020845	snp	A/C	0.00874735	0.0655527	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20883387	GTCCACCAACATACT[A/C]CATCAAGATATCTCC	10529
rs141028757	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20820448	TCACAGGGACAGTTT[C/T]AGTGTCTTTTTAGAC	10529
rs141038685	snp	A/G	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:20990714	AAAATTACTCACTAA[A/G]TGCAGCTTAGCCAGC	10529
rs141040103	snp	A/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21069001	TCAAGCAATCCTCCC[A/T]TCTCACTCTCCCGAG	10529
rs141044585	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20948629	AGACACACACTCACG[C/T]TGGAGGACACAAAAA	10529
rs141044602	snp	A/G	0.00438332	0.0466095	intron-variant	NEBL	GRCh38.p7	10:21056892	GGAGGGCTCCATGCA[A/G]TACAGCTAATCCCTT	10529
rs141056963	snp	A/G	0.0232847	0.105357	intron-variant	NEBL	GRCh38.p7	10:20953368	TCTGCAAGCCAGGAA[A/G]AGAGCCCTCACCAGC	10529
rs141074316	snp	C/T	0.180702	0.240204	intron-variant	NEBL	GRCh38.p7	10:21106791	CAGTATGGCCATTTT[C/T]AGGATATTGATTCTT	10529
rs141082880	snp	C/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21078632	CTATGACCTGCTCAT[C/T]TGAGTGGGACTTTAA	10529
rs141087453	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21099130	AGAGAAAGACCCTGT[C/T]TCTAAAAATAAAAAT	10529
rs141087494	snp	A/G	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21054882	AGAGTTAATTACCCA[A/G]GCACTGCAAGATAAG	10529
rs141089714	snp	A/C	0.00478085	0.0486577	intron-variant	NEBL	GRCh38.p7	10:21014449	GTTTAAGATTGGGCA[A/C]TCATACAGAGTGGGA	10529
rs141095591	snp	G/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20987975	CCTTATGAGATGATA[G/T]ACCATCTTCATGGAC	10529
rs141109088	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20974156	TCAAACCCAGATCTG[C/T]TGTCCCCAAAGTCTT	10529
rs141118366	snp	C/T	0.00636936	0.0560724	intron-variant	NEBL	GRCh38.p7	10:20829652	CACCAGGCTTCATTA[C/T]ACCCTCGTAAGTATC	10529
rs141126868	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:21059677	CAGGTTATTTACTGC[C/G]TTGATTAAAACTCTT	10529
rs141133486	snp	A/C	0.00914312	0.0669923	intron-variant	NEBL	GRCh38.p7	10:20824804	CAAAGGGACTCTAAT[A/C]AAAATGGCACAGTTA	10529
rs141143367	snp	A/G	0.0166325	0.0896639	intron-variant	NEBL	GRCh38.p7	10:21168942	TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGC	10529
rs141153708	snp	A/G	0.000297476	0.0121922	intron-variant, synonymous-codon, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20869833	CTGCACGTCTTTCCT[A/G]TAAGAAATCTGATCA	10529
rs141158982	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21061776	CAGAGTGGATAAGGA[C/T]TGAGCCACCTAAATA	10529
rs141170379	snp	A/G	0.00438332	0.0466095	intron-variant	NEBL	GRCh38.p7	10:20981204	GTCCTAAAGATAGAG[A/G]ACACATAAAGTTCAA	10529
rs141174244	snp	A/G	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:20909959	ATTAAAATAGTGAAT[A/G]AATATGTCCTTTGTA	10529
rs141175263	snp	G/T	0.00795532	0.062565	intron-variant	NEBL	GRCh38.p7	10:20966632	TGCAGGGTGACAGCC[G/T]GGACACCGGAGCAGT	10529
rs141182878	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21154415	AATGAGCTGAAATCG[C/T]GCCACTGCACTCCAT	10529
rs141192919	snp	A/G	0.0193772	0.0965046	intron-variant	NEBL	GRCh38.p7	10:20815817	TCTGTCACCCAGGCT[A/G]AAGTGCAGTGGTACA	10529
rs141197558	snp	C/T	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:21084436	AGCAAATATAAAAGG[C/T]CAATGTTAAAACTAA	10529
rs141209807	snp	A/G	0.02016	0.0983543	intron-variant	NEBL	GRCh38.p7	10:21007075	AAGGATAAACATTTC[A/G]GTGGAGAATGAGAGG	10529
rs141224763	snp	C/T	0.00835141	0.0640778	intron-variant	NEBL	GRCh38.p7	10:20819614	CACATGGCTACAGAA[C/T]ATTCATTAATAAGAT	10529
rs141236502	snp	A/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21163015	GATTGGATATTCCAA[A/T]GAATCCTTAATCCTA	10529
rs141237260	snp	A/G	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:21048388	ATGGTTGCCACTCAG[A/G]AAATCTCCCGGGGCG	10529
rs141253990	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21095016	TAGTGTATTCAAAAT[C/G]TGACACCACTAAGCA	10529
rs141285752	snp	A/G	9.92556e-05	0.007044	intron-variant, missense, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20858316	GAAACTGGATCATGC[A/G]TATTTTGAATGTCTT	10529
rs141291321	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21009265	TTTTTGTATAAGTAA[A/G]TCGCTTGGAATTGGT	10529
rs141292689	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20913190	TTAGAGCATTGACTC[A/G]GCTTAGAGAAGGGAG	10529
rs141293387	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20908373	AGGAATTGTCATTAC[A/G]GATGCTTATATAAAG	10529
rs141294379	snp	A/G	0.0240643	0.107019	intron-variant	NEBL	GRCh38.p7	10:20942321	TTTGACAAACCTGAC[A/G]AAAACAAGAAATGGG	10529
rs141295357	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20850989	ATTTTTTCATAGACA[C/T]TGAGTAAAACACTCA	10529
rs141306151	snp	C/G	0.0134861	0.0810011	intron-variant, upstream-variant-2KB	NEBL, LOC102725112	GRCh38.p7	10:20845438	AAGAGATTTGAACAA[C/G]AGTTCCCAGAACAAA	10529
rs141311959	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20781580	AACTGGATACCATGT[A/G]TCAAGCACAAAAAAT	10529
rs141313893	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20911660	TATAAGTGGATTTTA[C/T]ATGTACATAAAATAG	10529
rs141314080	snp	A/G	0.0146672	0.084371	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20854846	CTGGAATTACAGACA[A/G]GAGCTACTGCACCTA	10529
rs141325592	snp	A/C	0.127254	0.217792	intron-variant	NEBL	GRCh38.p7	10:20938619	GTTGAGAGAAGAAGG[A/C]TTCAGACAATCAAAC	10529
rs141339367	snp	A/C	0.00318978	0.0398085	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20899603	TCAATACACCTAAAG[A/C]CCTCTCTTTCACAGA	10529
rs141346867	in-del	-/ATC	0.0310518	0.120672	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20897996	AACATCGTTTCAAAA[-/ATC]ATCATCATCATCTTT	10529
rs141347111	snp	A/G	0.0115144	0.0749975	intron-variant	NEBL	GRCh38.p7	10:21108609	TTTTAGAATAAGTGT[A/G]ATGTGGTGCTAAGAA	10529
rs141351768	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21149182	GAACACTGTAGTGAG[A/T]ACTTCGGGGCAGCTG	10529
rs141355206	snp	A/G	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:21011451	TTCAACAACTGAAAC[A/G]GTCAGCTTAGGTCAA	10529
rs141358908	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20943847	AGCAAGCATCCTCAT[A/C]AGCTGGCAAAACATG	10529
rs141372265	snp	A/G	0.00755907	0.0610114	intron-variant	NEBL	GRCh38.p7	10:21080768	ATGGAATGATTATAT[A/G]CCCTCCCAACAGTGC	10529
rs141374990	snp	A/G	0.0402882	0.136092	intron-variant	NEBL	GRCh38.p7	10:21004677	GTGAGTCGAGATTGC[A/G]CCACTGCACTCCAGC	10529
rs141376023	snp	C/T	0.00279162	0.0372561	upstream-variant-2KB, intron-variant	C10orf113, NEBL	GRCh38.p7	10:21147953	GTCTTTAGGCAGTGA[C/T]GATACAATAATGTCC	10529
rs141377484	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20867863	ATTTCAGGACTCCCT[A/G]TTCTATCCTACTGAT	10529
rs141381455	snp	C/T	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:20802887	GTTTATTTAGGGCAC[C/T]TAGCTGAGGAAATGT	10529
rs141384401	snp	A/G	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21142684	CCCAACCCCCAGGGC[A/G]GCAGACGGTATGGCG	10529
rs141393863	in-del	-/AGACTTATGAGA	0.462034	0.132445	intron-variant	NEBL	GRCh38.p7	10:21032634	TGCCCTTCAGAAAGC[-/AGACTTATGAGA]GCTGCTGATAGATAA	10529
rs141400323	snp	A/G	0.046775	0.145601	intron-variant	NEBL	GRCh38.p7	10:21038532	CATGTCCCTGCAAAA[A/G]ACATGAACTCATTCT	10529
rs141424704	snp	A/C	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21155344	TTATTGACTATAATC[A/C]CCTTGTTGTGCTATC	10529
rs141432086	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20934562	CTATCCACGATGGGC[C/T]CGCTCTTTGCCTGAC	10529
rs141436990	snp	A/C	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:21041845	GAGGGTTCCTCCCCA[A/C]TTTAGACCATATATA	10529
rs141437666	snp	C/T	0.00636936	0.0560724	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20878549	CACTGAACCAAGAGA[C/T]GTACTTTCAAGACCT	10529
rs141444491	snp	A/G	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:21053304	AGTGATGTTAAGCAG[A/G]CTTCTTGGCTATAAT	10529
rs141454759	snp	C/T	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:20984092	ATGAAGTTTTGCAGG[C/T]AAACATCCAAAAATC	10529
rs141466950	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:20842626	ACAATTTATGGTTGC[A/T]TATATTTATGGGGTA	10529
rs141468745	snp	A/G	0.00835141	0.0640778	intron-variant	NEBL	GRCh38.p7	10:20948119	TTGAGTGTTGTTCCT[A/G]TTTTTAAATTTCTTT	10529
rs141478419	snp	G/T	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20840247	ATACAAGGATTACAG[G/T]ACTGAAAACACTTCA	10529
rs141486430	snp	C/G	0.0170251	0.090679	intron-variant	NEBL	GRCh38.p7	10:20806265	CAAGCAGAGGCCCTC[C/G]GAATTCCTGATCTCT	10529
rs141498166	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20931709	CTGACATGACATGGA[C/T]GAGGGTCTCAACAGT	10529
rs141499897	snp	A/G	0.00517822	0.0506191	intron-variant	NEBL	GRCh38.p7	10:20965234	CTTATGTTAATTACA[A/G]TGCAAGAGATGAAAA	10529
rs141505233	snp	A/G	0.00398564	0.0444627	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21141660	TTAAAAGCTGAAAAA[A/G]TAAAACTAAGAGACT	10529
rs141517547	snp	A/T	0.0352966	0.128072	intron-variant	NEBL	GRCh38.p7	10:21033257	GAAAAATATCAAAAC[A/T]AAGTTTATAAGAAAA	10529
rs141519477	snp	A/G	0.00795532	0.062565	intron-variant	NEBL	GRCh38.p7	10:21074070	ACAGAGTGAGACTCC[A/G]TCTCAAAAAAAAAAG	10529
rs141531477	snp	A/G	0.00120096	0.0244753	intron-variant	NEBL	GRCh38.p7	10:21091186	CAGTCAAGAAAACAA[A/G]TTCGTGTTTCACATT	10529
rs141533472	snp	A/C	0.00835141	0.0640778	intron-variant	NEBL	GRCh38.p7	10:21159363	TTGAACAAGCACAGC[A/C]TTTCCTTCTTCCCCT	10529
rs141546898	snp	A/G	0.0244538	0.107838	intron-variant	NEBL	GRCh38.p7	10:20935537	CACGGACTTTGGCAG[A/G]TCTCCTCCTTTGCAA	10529
rs141546991	snp	A/G	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:20998934	CAAGTTCTGGGGGCC[A/G]CCAACAAAACAGGAT	10529
rs141558769	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21035409	GTACAACCTTGTCAA[C/G]TACTGTGACCCCGAC	10529
rs141569654	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20848873	AAATTAAACAATTTT[A/G]TCTATTCAGTAAACC	10529
rs141574784	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20784994	GCAACAGGGTAAATG[C/T]TACTAGGGAAATTAT	10529
rs141585606	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21070224	TAATGCCCTTGAGTC[A/G]TCAGGACCTCAGTTT	10529
rs141594630	snp	C/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21034061	AGTCTCAGCTACTAG[C/G]GGGGCTGAGGTGGAA	10529
rs141602984	snp	C/G	0.0205511	0.0992634	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21137135	GTCTTAGTCCTGACT[C/G]TATCACTTACTGGCC	10529
rs141603509	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20881524	GAAGTAGATGTAACC[A/G]AACTCAACCACAAAG	10529
rs141612777	snp	A/G	0.0275645	0.114116	intron-variant	NEBL	GRCh38.p7	10:20796264	GCTTCTCAGGAGGCT[A/G]AGGAGAATCGCTTGA	10529
rs141617717	snp	A/G/T	0.0241112	0.107442	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21134123	CCCAGCTACTCAGGA[A/G/T]GCTGAGGCAGGAGAA	10529
rs141621075	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21068209	GTTGAACACTTTTAT[A/G]AAGTTAAAAAAGCAT	10529
rs141637099	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21098156	GGCTAAAGCTGCAGG[G/T]CCCTTTCATGTAGGA	10529
rs141647001	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21029783	GATCGCTATGATGAC[C/T]GAGGCAGCAGAGACT	10529
rs141649218	snp	C/T	0.00993419	0.0697739	intron-variant	NEBL	GRCh38.p7	10:20964752	AGTTGCTGACTACCA[C/T]GTGGCCACTGTCCAA	10529
rs141655771	snp	C/T	0.0244538	0.107838	intron-variant	NEBL	GRCh38.p7	10:20937516	TCCCAGTGTGAGTGA[C/T]GCAGAAAACAGATGA	10529
rs141658187	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21076640	GAATGAATCAGAAAA[C/T]AGAATGTGATATACA	10529
rs141660360	snp	C/T	0.00953873	0.0683987	intron-variant	NEBL	GRCh38.p7	10:21072851	CAAAAGTTAGCCAGG[C/T]GTGGTGGCAGGCACC	10529
rs141664885	snp	A/C	0.0221141	0.102801	intron-variant	NEBL	GRCh38.p7	10:20962254	AAGCCTCATTTTGAG[A/C]CTAAACTGCCCTATG	10529
rs141681076	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20799648	CTCTTGCTGAATGCA[A/C]ATTCTTTACAGAAGT	10529
rs141693144	snp	A/C/G	0.00358938	0.0422398	intron-variant	NEBL	GRCh38.p7	10:20892306	AGATGCTGCACAACC[A/C/G]TGTGACATTCTGTCT	10529
rs141699718	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20828098	AAAAAAAAGTGCTGA[C/T]GCAATTCCTCTTCCT	10529
rs141707642	snp	A/G/T	0.016574	0.0895128	utr-variant-5-prime, upstream-variant-2KB	NEBL, NEBL-AS1	GRCh38.p7	10:21173840	GGGGTTCATGATCGC[A/G/T]GTTCCCGGGGGCGGC	10529
rs141707690	snp	A/G	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:20828372	TGATAATTTGTAAAA[A/G]TTATCAGTATTCTTA	10529
rs141711606	snp	A/G	0.00914312	0.0669923	intron-variant	NEBL	GRCh38.p7	10:20885676	GGAAACATCGGAAAA[A/G]TTACCTTCCCAAGGA	10529
rs141718287	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20891228	CAGATGCCTACCACA[C/T]TAAACATTTGCTTTA	10529
rs141724224	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20827244	AATCCAGTGGCCCCC[A/G]CGTGGGTGGGAGAGC	10529
rs141725844	snp	A/T	0.00279162	0.0372561	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21139085	AGAACACGCTCAGTC[A/T]TCTCTAGTTACAATA	10529
rs141742724	in-del	-/AAC/AC			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20855521	TAAGAAAACAAAACA[-/AAC/AC]AAACAAAAAAAAAAC	10529
rs141761525	snp	C/T	0.130694	0.219696	intron-variant	NEBL	GRCh38.p7	10:21080999	AGCTGGGTCTACAGG[C/T]ATGCACCACCACGCC	10529
rs141764161	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20795041	ACCCAAACTCTTGAC[A/T]ATACTAAACCTAAAT	10529
rs141770352	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	NEBL	GRCh38.p7	10:21176026	ACAGGGTCTAACTCT[G/T]TCACCCAGGCTGGAG	10529
rs141770489	snp	C/T	0.00119737	0.0244387	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21133394	TGAAATGTGACCTGT[C/T]ACAATTTCTCTATGA	10529
rs141772225	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21016068	TGAATGGGCTGCTGC[A/G]GGCCCGTGGGGGCGT	10529
rs141788959	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21065819	CACTCCATCTGGCAC[A/G]TCTTTCCTGGAACAG	10529
rs141796433	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20917389	GGCAAAGAATTTTTC[A/G]TCTTTTTCACTGATA	10529
rs141802033	snp	A/G	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:20833403	CTATGGCAAAGTCCC[A/G]AACATTGGTTGAAAA	10529
rs141813108	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20978480	ATTTAGAAAGGGCTG[A/G]GTGCAGTGGCTCACA	10529
rs141819325	in-del	-/C	0.0283406	0.115616	intron-variant	NEBL	GRCh38.p7	10:20800347	GTATGTGTATATATA[-/C]CACATTTTCTTTACC	10529
rs141824968	snp	A/G	0.0252325	0.109451	intron-variant	NEBL	GRCh38.p7	10:20921156	GAAACAAATGCTGAT[A/G]TTTTATTTAAACTGT	10529
rs141849321	snp	C/T	0.0197687	0.0974348	intron-variant	NEBL	GRCh38.p7	10:20919773	GGAAACCATTCCTAA[C/T]TCAAAATCCGGAACC	10529
rs141849538	snp	G/T	0.00835141	0.0640778	intron-variant	NEBL	GRCh38.p7	10:21118060	ATTATGATTTCCTCA[G/T]GTGCCCACTGAGAAG	10529
rs141866716	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20924332	ACAACTTACAGTACC[C/T]ATCTGCTTTGTATCC	10529
rs141877196	snp	C/T	0.0107246	0.0724382	intron-variant	NEBL	GRCh38.p7	10:20951027	GTAATCCCAGCACTT[C/T]AGGAAGCTGAGATGG	10529
rs141877394	snp	A/C	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:21021149	CCAATCACTCGTTCA[A/C]CAAATCTATTGATCT	10529
rs141882833	in-del	-/TGAGTTTACC	0.377385	0.215112	intron-variant	NEBL	GRCh38.p7	10:20887224	CTTCTGGATTCAAAA[-/TGAGTTTACC]TGATGACAATTCTTA	10529
rs141888058	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20922314	ACCCATGGCTGTTGT[G/T]AGGCTCTGAATGCAC	10529
rs141889320	snp	G/T	0.000798403	0.0199641	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20876401	ACTAATATATCTAAT[G/T]TTAATGCTAAATCCT	10529
rs141895668	snp	C/T	0.00597247	0.0543191	intron-variant	NEBL	GRCh38.p7	10:20824215	ATATGAAAGCATAGG[C/T]TCAACTTAAGAGGCC	10529
rs141907640	snp	C/G	0.0236746	0.106192	intron-variant	NEBL	GRCh38.p7	10:20838437	AATCAAACTTGAATG[C/G]ATAAGGAGTTGCTTC	10529
rs141913799	snp	A/G	0.0107246	0.0724382	intron-variant	NEBL	GRCh38.p7	10:20916302	CAGAAGCAAACTATC[A/G]CTTAAAAATTAAATA	10529
rs141936641	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21164080	TTAGCAGGACTTTGC[G/T]GAATTCAAATAGCCA	10529
rs141949297	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20787819	GCAACACGTTTGTTC[A/G]GTAGTTAACAAAAAG	10529
rs141949599	snp	A/G	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:21017344	TTCTTGAATTGCATT[A/G]AATTTCCCCATGTTG	10529
rs141954107	snp	A/G	0.0134861	0.0810011	intron-variant	NEBL	GRCh38.p7	10:21120599	TTAATTACTAGGGCA[A/G]TCATAAAATACCGGT	10529
rs141956727	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21121831	ACCAGGATACCAAAA[C/T]GAAGTGATAGAAAAT	10529
rs141963172	snp	A/G	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:21056727	TGCAACATTAAAGCT[A/G]TATGGATGCATCTCA	10529
rs141982885	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21020779	GCTGCTCCCTCTAGT[A/G]GTTCCTTCCCTGTCT	10529
rs141986063	snp	A/C	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:21086290	GATTTGTGTAAGGAG[A/C]AATCAATGACATAAC	10529
rs141999054	snp	C/G	0.000798403	0.0199641	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20879460	TCTTAAACTATGTTA[C/G]AAAAGTGCTCTGCTT	10529
rs142000151	snp	C/T	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:21118254	TAATCCCTTCCTTAT[C/T]GTTCTTTCAACATGG	10529
rs142006176	snp	A/G	0.0410537	0.137264	intron-variant	NEBL	GRCh38.p7	10:20812444	TCATTTACATTAGGT[A/G]TATCTCCTAATGCTA	10529
rs142013514	snp	A/G	0.00478085	0.0486577	intron-variant	NEBL	GRCh38.p7	10:21115784	AGCCACTATTTCTTT[A/G]GATTTTTTTCTGTTC	10529
rs142027786	snp	A/T	0.0115144	0.0749975	intron-variant	NEBL	GRCh38.p7	10:21051293	CTGTATGATTTAAAA[A/T]ACAAATGCATAAAAT	10529
rs142063402	snp	A/G	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:21156896	CCCCTTCTTTTTAAA[A/G]TAAAACAAGAACTAT	10529
rs142064954	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21014894	CTTCCTATGAACCAC[A/G]TTTTCATGCCTCTGC	10529
rs142066242	in-del	-/ATA	0.0410537	0.137264	intron-variant	NEBL	GRCh38.p7	10:20822646	TACAGACTATCTAAT[-/ATA]GGCTATATATAGATA	10529
rs142067613	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21053904	CAGGCATGGTGGTTC[A/G]CACCTGTAATCCCAG	10529
rs142088931	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20986417	CCCTTCAAAATTCCC[A/C]AAGTACTTTTCAATT	10529
rs142094437	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:20807982	TAGTATTTCTCATTT[-/A]AAAAAAAAAAAAAAC	10529
rs142103601	snp	C/T	0.00358779	0.0422022	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20879096	TTCTTTCCTGCAGTG[C/T]GTTTGAAATCTGAAG	10529
rs142104081	snp	A/G/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20904795	TGGAAAAACTTGAAT[A/G/T]TGAGAGTGGATTTAT	10529
rs142105680	snp	A/C	0.0314385	0.121371	intron-variant	NEBL	GRCh38.p7	10:20812350	ATTATACTTGAAGTT[A/C]TAGGGTACATGTGCA	10529
rs142110233	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20817979	AATCATAAGGCAACA[C/T]GCTTTAAAAGAAACG	10529
rs142116662	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20780842	CATCTGTCATTCCTG[C/G]TTTGCCGTCATTTAA	10529
rs142124335	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20807142	CCAGCATGGACAACA[C/T]TGCGAGACCCCCGTC	10529
rs142131159	snp	C/T	0.00557542	0.0525036	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20878085	CTGTTTGGAGATCAT[C/T]TAATTTTGGGGTGGC	10529
rs142138590	snp	A/C/T	8.24287e-05	0.00641931	NEBL, LOC102725112	10	allele_origin=A(germline)/C(germline)	10:20868723	GTCTTCCAATTACAG[A/C/T]GGGCTCTTTATTCAT	10529
rs142144637	snp	A/C	0.00953873	0.0683987	downstream-variant-500B	NEBL	GRCh38.p7	10:20779833	GGAAAAAAAAAAAGT[A/C]TCAGAGGGAAAAAAG	10529
rs142145772	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20811094	AGCTGGCTCATTGGA[A/C]AGTTTAATGTTGGCC	10529
rs142147440	snp	C/T	0.0314385	0.121371	intron-variant	NEBL	GRCh38.p7	10:21155031	TGGTGAAACCCCATA[C/T]CTACTACAAATACAA	10529
rs142157051	snp	G/T	6.59924e-05	0.00574385	intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20826452	GAGAACTTACTGAAC[G/T]AATATTCTGCTGATT	10529
rs142164649	snp	A/G	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:21036069	TCAGGGAGCCGAGGC[A/G]GGAGAATCACTTGAA	10529
rs142167688	snp	C/G/T	0.000167938	0.00916215	missense, intron-variant	C10orf113, NEBL	GRCh38.p7	10:21126106	CCCTTCTCGGCTCTC[C/G/T]GTTCTGCCTTACCAG	10529
rs142168409	snp	C/T	0.0197687	0.0974348	intron-variant	NEBL	GRCh38.p7	10:21094100	GGTAGCTCACGCTTG[C/T]AATGCCAACACTTTG	10529
rs142169654	in-del	-/A	0.104859	0.203554	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20863714	CCATAATAGTGGATC[-/A]AAGGCATATGAGCCC	10529
rs142170561	snp	C/T	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:21162154	GGTTGATGATTGCAC[C/T]AATGTGCCAGGAAGA	10529
rs142182267	snp	A/C	0.00478085	0.0486577	intron-variant	NEBL	GRCh38.p7	10:21157816	TTGCTGAGGTAATCA[A/C]GTGAGAATGAGGTCA	10529
rs142185098	snp	C/T	0.0185938	0.0946107	intron-variant	NEBL	GRCh38.p7	10:21001015	GAATTCGCTCCTGCA[C/T]ACCCAATCATCTGCA	10529
rs142189805	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20936527	ACATAATTAACTATG[C/T]CTGTTCCCCACTTCC	10529
rs142216997	snp	C/T	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:20963977	CCATTCATCAGCTCT[C/T]TCTTTTCCACACTCC	10529
rs142230302	in-del	-/AT	0.0275645	0.114116	intron-variant	NEBL	GRCh38.p7	10:20798474	GACAGGTAAGTATGC[-/AT]ATATCTGTTCAGTCT	10529
rs142232529	snp	C/G	0.00676609	0.0577691	intron-variant	NEBL	GRCh38.p7	10:20906376	GGGAAAACAATACTA[C/G]TGATGCTCAGAAGTT	10529
rs142253096	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20797564	CAACATGATCTCAAG[A/G]TACAGAAATACGAGA	10529
rs142253402	snp	C/T	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21136604	AGCTTCCCCACCTCT[C/T]CTTCTGTATCCCTGT	10529
rs142259011	snp	A/G	0.0126979	0.078662	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20960681	TATTTATATATAAAT[A/G]CATATATAATATATA	10529
rs142261177	snp	C/G	0.0123036	0.0774623	intron-variant	NEBL	GRCh38.p7	10:20905184	AAACTAGATGATTTG[C/G]CACTTTTTGGAGAAA	10529
rs142268237	snp	C/T	0.0150606	0.0854603	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20877140	AAAGTAGAAGGAGGA[C/T]GAAATAGAACCAGTA	10529
rs142270288	snp	C/G	0.00993419	0.0697739	intron-variant	NEBL	GRCh38.p7	10:20908970	ATCACCAGACACTGA[C/G]ATCATAAAATTTGTG	10529
rs142271514	snp	C/T	0.0119091	0.0762411	intron-variant	NEBL	GRCh38.p7	10:21040248	GCGGGTGCCTGTAAT[C/T]CCAGCTACTTGGGAG	10529
rs142275960	snp	C/T	0.00438332	0.0466095	intron-variant	NEBL	GRCh38.p7	10:21099187	TACCTTTTTCATAGA[C/T]ATATCATTTTTTAAA	10529
rs142279732	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20809440	TTCTACTGTTCTATA[C/T]ATAATTCTTTAAATC	10529
rs142291211	snp	C/T	0.0162398	0.0886349	intron-variant	NEBL	GRCh38.p7	10:20938284	TTTGCTGCTCACCAA[C/T]GTCTGCTGTTCTGCA	10529
rs142298454	snp	C/G	0.0111196	0.0737302	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20882920	ATCTATCTCCCCCTA[C/G]CTGCGTCTATGTGGC	10529
rs142300825	snp	G/T	0.0123036	0.0774623	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20875196	TTTAATCTCAGCTTG[G/T]TCTCTCCTTATAATC	10529
rs142302895	snp	A/G	0.0166325	0.0896639	intron-variant	NEBL	GRCh38.p7	10:20907714	TTTTCCTATTTTAAA[A/G]GAAATTTAAAAATTT	10529
rs142304319	snp	C/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21078021	TCCAGAGCACGGATT[C/G]ACTCTCAATACCAGA	10529
rs142310070	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20807947	GTATATAAAATAGTG[A/G]CAAGATTATTAACAA	10529
rs142345751	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21000807	TGCTGTTTTTGCAGT[C/G]TAAGATATGGAAGAA	10529
rs142345889	snp	A/C	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:21107381	TTTTAGCATGAAGAC[A/C]TGTTGAATTTTGTCG	10529
rs142346030	snp	A/G	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:21066783	TAATTCCCATCTACA[A/G]AATCATTGTTCTCTT	10529
rs142359061	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21067757	TGAGGCAGGCAGATC[A/G]CTTGAGCCCAAGAAT	10529
rs142360473	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20892595	AACACCAAAAGACAA[A/C]AAGGGCAAAATTGAT	10529
rs142369372	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21001766	TCAAAAACCTGCAAC[C/T]TCAGACATGAATGGA	10529
rs142374960	snp	A/G	0.00119737	0.0244387	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21146256	CTCTTACAGCTGCAC[A/G]TGTCAGGCAGCATCA	10529
rs142381939	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20801839	TTACATGGGATGAAA[C/T]GCCGGAAGCATAGCC	10529
rs142384588	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21002889	TAAACCATATCATCA[A/G]TTAGTGAGGTCTCTT	10529
rs142387654	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21069242	GCTCCCAGCTTTCTG[C/T]GCTGGTTGCCCTTAG	10529
rs142397649	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20976676	ATGTAGAAACAGAAA[A/G]CCAAATACCACATGT	10529
rs142401270	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21103993	AGTGCTCAGGTTTTG[C/T]TTTGTTTTCTTTTCA	10529
rs142406839	in-del	-/AAAAAAAAAAC			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20875618	CAGAGAAAAGCAAAA[-/AAAAAAAAAAC]CCTCCACAGACTCTC	10529
rs142417379	snp	A/G	0.00517822	0.0506191	intron-variant	NEBL	GRCh38.p7	10:21105081	GAAACCCCACTTGGC[A/G]ATGATATTATCTTTT	10529
rs142431040	snp	A/T	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:21018563	CTATTCATGGCATTA[A/T]TAACCAACAGTAAAT	10529
rs142436574	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20998128	CATATCACTGATACG[A/G]TACGGTATGGAAATC	10529
rs142442241	snp	C/T	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:20990742	AGCCTAGCAAAATGA[C/T]ATTTTTCTTTCTGTC	10529
rs142451855	in-del	-/AT	0.0146672	0.084371	intron-variant	NEBL	GRCh38.p7	10:20904651	CATGTGTGCTTGTAC[-/AT]ATATGTACATTCACA	10529
rs142458643	snp	A/G	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20919078	CAAATGCCTTAAGAT[A/G]CAATATGATAATTAA	10529
rs142461920	snp	G/T	0.000298285	0.0122087	intron-variant, utr-variant-5-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20897239	TTATATTTTTAAAAT[G/T]TACTCATGTGGCGTC	10529
rs142469959	snp	A/C	0.0329836	0.124112	intron-variant	NEBL	GRCh38.p7	10:20836127	TGCTTGTCAAGCAAG[A/C]CTATCGGTGCTATTT	10529
rs142479366	snp	C/T	0.0452528	0.143452	intron-variant	NEBL	GRCh38.p7	10:21082793	TTTGAGACAGAGTCT[C/T]ACTCTGTCACCAAGG	10529
rs142499645	snp	C/T	0.00914312	0.0669923	intron-variant, upstream-variant-2KB	NEBL, NEBL-AS1	GRCh38.p7	10:21172087	ACTTCAGAGCCCACA[C/T]GTTCTCAGTGGGGAA	10529
rs142505137	snp	C/T	1.65075e-05	0.00287289	intron-variant, synonymous-codon, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20852551	AGTGTGTACCTGACT[C/T]TGGAGGACGGCATTG	10529
rs142508967	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20862067	ATACTGTAATGAAAG[C/T]GAAAGGCAGAATCAT	10529
rs142511523	snp	G/T	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:21118984	TCTTACAACAATCTT[G/T]TGAGCTAAGGACTTG	10529
rs142513078	snp	C/G/T	0.00398691	0.0444912	intron-variant	NEBL	GRCh38.p7	10:20798800	TCCTTCACACACATA[C/G/T]GGAACCCTTTGACTG	10529
rs142522957	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20863291	TCTGTGACTCAGAAT[C/T]GCAAAAAGCCAGCAA	10529
rs142525399	snp	C/T	0.0154538	0.0865337	intron-variant	NEBL	GRCh38.p7	10:20799782	TTAAATGAAGATACA[C/T]AGTTCTAAATCAGGA	10529
rs142525758	in-del	-/AC			intron-variant	NEBL	GRCh38.p7	10:21005169	CCCTGACTTGTGCAG[-/AC]ACACACACACACTCA	10529
rs142534615	in-del	-/GAGAA			intron-variant	NEBL	GRCh38.p7	10:21095332	GCCTAAGAAAAGCAG[-/GAGAA]ATAAAAGATAAGACG	10529
rs142535006	snp	C/G	0.000798403	0.0199641	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21137603	GTTACTACCTCCTTG[C/G]CCACTTCTGATAGGT	10529
rs142542513	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21022407	AGCCTACCCAAAGCA[C/T]GCTAGCACTTGCGAA	10529
rs142548743	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20934174	CACAGACAGGTCTAC[A/G]GTCAAAACAAAAGGC	10529
rs142551783	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20877591	TTGTGACAATAGGAA[A/C]AGGCTGCCTGGGAGT	10529
rs142560415	snp	A/C	0.00835141	0.0640778	intron-variant	NEBL	GRCh38.p7	10:20789972	ATATATATATATACA[A/C]ACACACACATACAAG	10529
rs142567026	snp	C/T	0.00478085	0.0486577	intron-variant	NEBL	GRCh38.p7	10:21169881	AACATTCTATACAGG[C/T]ATGTTGAGAGTATTA	10529
rs142570624	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20839620	TAGCTGAGATTAAGG[C/T]CATGTTTTAAACACA	10529
rs142573044	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21099853	AGCCAGCCCAAGATA[C/T]TACAGTCACTGAAGT	10529
rs142596544	snp	C/T	0.0111196	0.0737302	intron-variant	NEBL	GRCh38.p7	10:20821696	AAGATTGTCAGTAAG[C/T]CACATAATATCTACC	10529
rs142614670	snp	A/C	0.00914312	0.0669923	intron-variant	NEBL	GRCh38.p7	10:21071368	AAAATTTTAATTTAC[A/C]CACACACTCCTTTGT	10529
rs142619510	snp	C/T	0.0111196	0.0737302	intron-variant	NEBL	GRCh38.p7	10:21124683	CAAGGCCGAGCATAG[C/T]GGGTCATAGCTGGAA	10529
rs142625859	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21033321	GATTCCTTTGATAAA[A/G]ATAATAAATAAGTAT	10529
rs142629899	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21058067	ACAGCCAGTTGCAAT[C/G]AGCTCAGCATGTTTT	10529
rs142636682	snp	A/C	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:20891566	TGCTTGTGGCTACAG[A/C]CTCCTGATAAAGTCT	10529
rs142647547	snp	C/T	0.00914312	0.0669923	intron-variant	NEBL	GRCh38.p7	10:20892337	TCCACATTTTTCTTT[C/T]TCAATCAAAGGGAAG	10529
rs142662266	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20893090	ATGCAGATGAACACC[C/G]TAAACAGCCTTGAAC	10529
rs142663426	snp	C/T	0.00597247	0.0543191	intron-variant	NEBL	GRCh38.p7	10:20795782	AGTCACTGTGTACAA[C/T]GCTGCCTGAAAAAGA	10529
rs142670478	snp	A/G	0.00119737	0.0244387	intron-variant, downstream-variant-500B	NEBL, LOC102725112	GRCh38.p7	10:20880190	AGATGGTGAAAACCC[A/G]TCTCTACTAAAAATA	10529
rs142675080	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20888806	TTGCTCTGCAATTAA[C/T]TCCTTCAGGAAACAT	10529
rs142676001	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20852265	CATGTGGTTTGACCA[C/T]AGTTTAATTAATTCC	10529
rs142680356	snp	C/T	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20789448	TCTCACACTCTGTAA[C/T]ACATTTAGGTTCACC	10529
rs142682003	snp	A/G	0.00953873	0.0683987	intron-variant	NEBL	GRCh38.p7	10:20950485	CCTCTTCTCCCTCAT[A/G]AACACTTTTACATCC	10529
rs142682153	snp	A/C	0.00795532	0.062565	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20861054	CTTTAAAAAAAGAAA[A/C]ACTGACTTTTTTTAT	10529
rs142687497	snp	G/T	0.0539704	0.155153	intron-variant	NEBL	GRCh38.p7	10:20894820	TGTGGTCCCGGCTAC[G/T]CGGGTGGCTGAGGCA	10529
rs142692026	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20797380	GACCCTTAGACAATA[C/T]CATCAATCCATAAGG	10529
rs142693565	snp	C/T	0.000428421	0.0146297	missense, intron-variant, utr-variant-3-prime	C10orf113, NEBL	GRCh38.p7	10:21125887	TTTATGCCCTGGAAT[C/T]TAAATCCATGCTTCC	10529
rs142700931	snp	C/G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20791842	ACTGGGGGGGATGTA[C/G/T]GCAGAGTGCGTGAAA	10529
rs142701449	in-del	-/G	0.0130921	0.0798413	intron-variant	NEBL	GRCh38.p7	10:21047035	GTGTTATATTTTCAA[-/G]GAAGTATGGTTTACA	10529
rs142711691	snp	A/G	0.000798403	0.0199641	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21127634	TTTATATGAAACATG[A/G]GGATAGAGGCACAAA	10529
rs142734400	snp	C/T	0.0134861	0.0810011	intron-variant	NEBL	GRCh38.p7	10:20974705	ACTACCAATTAGATG[C/T]TCAGTAGGTGTCCAT	10529
rs142737420	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21043013	AGAGAAGGTGGAAAA[G/T]TCTGCTGTGTATGCA	10529
rs142744485	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21159039	ACACTCAGTGATCCA[C/T]CTTTTAAACTGTGTG	10529
rs142754277	in-del	-/ATAAAT	0.431473	0.171952	intron-variant	NEBL	GRCh38.p7	10:21063890	TAAATAAACAAATAA[-/ATAAAT]ATAAATATAAATATA	10529
rs142762603	snp	C/T	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:21049192	TTAAAAAAATCTTCA[C/T]AGCAACATATAGACA	10529
rs142764583	snp	C/T	0.00517822	0.0506191	intron-variant, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20884729	ACCGTGGATGAAACA[C/T]AGACTCTCATTAAGC	10529
rs142767702	snp	C/T	0.00795532	0.062565	intron-variant	NEBL	GRCh38.p7	10:21170433	TTCACTTTCCTTTAA[C/T]CAAAGAACAATTATC	10529
rs142775031	snp	A/C			intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20898087	ATTACTCAATGGGCA[A/C]CCCACATTCAGAAAA	10529
rs142776455	snp	A/G	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21075200	GAATGGCAAACCCAC[A/G]GTGGAAACACAATGG	10529
rs142777593	snp	A/T	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:21031654	CCACATCAAGAACAG[A/T]ACAGAGTCAGCCACT	10529
rs142779440	in-del	-/T	0.0134861	0.0810011	intron-variant	NEBL	GRCh38.p7	10:20993240	TCATGCAACCTCTGG[-/T]CATGAAAGTTTTGCT	10529
rs142802364	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21052985	AACAATATATTGTCT[A/G]TTTCAAAACAGCTAG	10529
rs142805538	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21077168	AGTTATTGGGGTCTA[G/T]CTTGGTTTTTATTCT	10529
rs142814950	in-del	-/C	0.0543475	0.155628	intron-variant	NEBL	GRCh38.p7	10:20981088	AGCCACTGTGCCCAG[-/C]CCCAACAAATTATTT	10529
rs142826473	snp	A/T	0.00716266	0.059414	intron-variant	NEBL	GRCh38.p7	10:21086794	AAATAAAAATAAAAA[A/T]AAATTACTGGAAATC	10529
rs142832161	snp	C/T	0.0103295	0.0711199	intron-variant	NEBL	GRCh38.p7	10:20968507	CAGAGCAAGACCCCA[C/T]CTCTAAAATAATTAA	10529
rs142835442	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20971397	CTTTATATGATTATA[A/G]TTTTTAAATATAAAT	10529
rs142836209	snp	A/G	0.00914312	0.0669923	intron-variant	NEBL	GRCh38.p7	10:20911470	ACATTTCAGAAACTA[A/G]CCAGGTATGCCTGAA	10529
rs142850200	snp	A/C	0.0383715	0.133092	intron-variant	NEBL	GRCh38.p7	10:20809130	TTCTATTCACATCAA[A/C]AATTAAATATAGAGT	10529
rs142853031	snp	A/G	0.00835141	0.0640778	intron-variant	NEBL	GRCh38.p7	10:21074758	GCTGGGATTATAGGC[A/G]TGAGCCACTGCACCT	10529
rs142860463	snp	C/G	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20979507	TACTCGTATAATTCT[C/G]AGAAGAGATCTAATA	10529
rs142864999	in-del	-/TAATAA			intron-variant	NEBL	GRCh38.p7	10:21092587	TTTACCTCTATAATT[-/TAATAA]TAATAATAATAATAA	10529
rs142876078	snp	G/T	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:20921559	CCTCCCACAATTCCA[G/T]TTCTCCATGGGCTTC	10529
rs142886021	snp	A/T	0.00874735	0.0655527	intron-variant	NEBL	GRCh38.p7	10:20837706	GGAGAAGTCAATGTC[A/T]GCTTCAATTCTTCAA	10529
rs142890577	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20811808	TATTCTTTAAGCTAC[A/G]TAACTACATAATTCA	10529
rs142893610	snp	G/T	0.00478085	0.0486577	intron-variant	NEBL	GRCh38.p7	10:21110547	TTTTTTCTTAATCAT[G/T]CTGCCTATTCAGCGA	10529
rs142897488	snp	A/G	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:21155805	ATCACATGGTCATTC[A/G]TGTTTCCACTTATTG	10529
rs142908049	snp	A/G	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:20905846	GGAGAGCTACATGAC[A/G]GAAATGTATAGAAAT	10529
rs142913849	snp	C/G	0.0103295	0.0711199	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20847389	AGAGTGAGAGAAGAA[C/G]TTGGGTGAAGAAAAG	10529
rs142920810	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20945918	ATTAAATAATTCATT[C/T]ATCCTCTCTAAATGC	10529
rs142928659	snp	C/G			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20881303	TTTTCAAATGATTGG[C/G]TCTGATTTTATGTAG	10529
rs142953403	snp	C/G	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:21050598	CAAAATAAAGAAAGT[C/G]AGGAACGGGTGCAGC	10529
rs142954785	snp	A/C	0.00636936	0.0560724	intron-variant	NEBL	GRCh38.p7	10:20835016	AGACCTCCATCCAAA[A/C]TGCTGACTGTGTAGA	10529
rs142961628	snp	A/G	0.00517822	0.0506191	intron-variant	NEBL	GRCh38.p7	10:20955431	TCAGGGGGCTGGGCT[A/G]TCATTTACAGATAGT	10529
rs142986983	snp	C/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20804510	AAACTAACCAAGCAC[C/G]GTTCCACTTAAGAGA	10529
rs142991876	snp	G/T	0.00159617	0.0282053	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20780042	TACAATTAGGAAGGA[G/T]TATGAGCCAAAGAGA	10529
rs142996845	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21115462	AATTCTTTCAGCTTT[C/T]GTGTGTCTGGGAAGG	10529
rs143003054	snp	A/G	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21138214	CTGTCCCAACTCACC[A/G]TAAACACTGCAAAAT	10529
rs143007421	in-del	-/AAAAAAC			intron-variant	NEBL	GRCh38.p7	10:21069382	ACCATGTCACATAAA[-/AAAAAAC]CCACAGCCAGTAGAG	10529
rs143012792	snp	C/T	4.95503e-05	0.00497722	intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20813959	AAATATGATTTTGTG[C/T]TTCTTTAACATGTCT	10529
rs143020667	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:21042664	TTTACCATGGTGGGA[C/G]TATTTTTCACCACAG	10529
rs143024608	snp	C/G	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21110191	ATCAAGGTCATGCTG[C/G]CCTTGTGCCCACTTC	10529
rs143026145	snp	A/T	0.02016	0.0983543	intron-variant	NEBL	GRCh38.p7	10:20949403	AACCACCATGGCACA[A/T]GTATACCTATGTAAC	10529
rs143029785	in-del	-/A			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21134235	ATCTCAAGAAAAAAA[-/A]AAAAAAATCTAAGTA	10529
rs143038646	snp	A/C	0.0205511	0.0992634	intron-variant	NEBL	GRCh38.p7	10:20936103	AAAGCATTTCCATGC[A/C]AAAATCTTTCCTCCA	10529
rs143039229	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21006229	TGTGCTACTACAAAC[G/T]GTGCTGTCATAGACA	10529
rs143072630	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21002523	TTAGTCCATTCTCAC[A/G]CTGCTATAAAGAACT	10529
rs143076739	snp	A/G	0.0236746	0.106192	intron-variant	NEBL	GRCh38.p7	10:20937428	TGTTCAGCTGAAACA[A/G]GTCACTTCAAAAGTT	10529
rs143082694	snp	G/T	0.0221141	0.102801	intron-variant	NEBL	GRCh38.p7	10:20843027	AACTAAATGTTTCTG[G/T]CCCACCAAAACCCGT	10529
rs143083526	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21028604	TAAGATCTTTCTATC[C/T]TTCATGAGAAAGGTT	10529
rs143086012	snp	A/G	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:20925088	AGCCCCGGAAATAAA[A/G]TAATACCTCAGACCC	10529
rs143087890	snp	C/T			intron-variant, utr-variant-5-prime	NEBL	GRCh38.p7	10:20958077	TGAATGCATTGCTTG[C/T]AAACTTGAAGGTGGG	10529
rs143095396	snp	C/T	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:21148604	GATCTCAGCTCACTG[C/T]AACTTCCACCTCCTG	10529
rs143116496	snp	C/T	0.00953873	0.0683987	intron-variant	NEBL	GRCh38.p7	10:20836263	AGTCTTGCTCTCTCG[C/T]GCAGGCTGGAGTGCA	10529
rs143120150	snp	A/C	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20978165	GCTAAAAGACAGACC[A/C]GAAATGAGATTCAAG	10529
rs143127533	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20927083	GGAGTTTCAACGCGA[A/C]TGCATGTGGAGAGAC	10529
rs143129743	snp	C/T	0.00874735	0.0655527	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20872421	GCTTATGTTGGGGGA[C/T]ATTCAAGAGGGTGAC	10529
rs143149169	snp	A/C/G	0.000247477	0.0111213	intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20808524	CCTCCTTCATCAGAC[A/C/G]GTCTTGTTACCTCAC	10529
rs143157555	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20802751	AATCAGAACTTACTC[A/G]AAAGAAGGAACGAAA	10529
rs143159372	in-del	-/T			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21132933	ATTCTACGGGTAGTC[-/T]TTACACTTTCTTGAG	10529
rs143167286	snp	C/T	0.0170251	0.090679	intron-variant	NEBL	GRCh38.p7	10:20931569	GCCATGGCTGTGGCC[C/T]GGAAAAAGTCCAGGC	10529
rs143179922	snp	A/G	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:20786901	CCATGCTCCTAAGGC[A/G]TGAGTAAAGAGCATA	10529
rs143189381	snp	C/G	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20837422	ACCCTCCTCATTTCT[C/G]TGAAGGCTGAGAGAG	10529
rs143202981	snp	C/T	0.0134861	0.0810011	intron-variant	NEBL	GRCh38.p7	10:21155038	ACCCCATATCTACTA[C/T]AAATACAAAAATTAG	10529
rs143207533	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20933283	AAAGAAAGTGTCAAT[A/T]TTTTAAGCCATCAGA	10529
rs143209133	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21085192	ACGCTCCATCACATG[C/T]TAATCTTGAAACATT	10529
rs143220860	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21030663	TAAAGTAGGTGTGGT[C/G]AATGTCCCAAAAGAC	10529
rs143232031	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20959310	TTTCAGGATTATAAT[C/T]TCCCAGCATCTCTAG	10529
rs143238765	in-del	-/AG	0.00438332	0.0466095	intron-variant	NEBL	GRCh38.p7	10:20902850	CAGCTTGACTCCCAC[-/AG]AGTGTCCCTTTCCTA	10529
rs143249531	snp	A/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21025535	GGAAAAGTTATATGC[A/T]AATCACTAGACCTCG	10529
rs143265801	snp	C/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21056981	TCAATTTAAAGCTTT[C/T]TGCATATATGATATA	10529
rs143267268	snp	A/C	0.0209421	0.100162	intron-variant	NEBL	GRCh38.p7	10:20935241	TTTGTATAATACACA[A/C]CATGGGTATCAATAA	10529
rs143272673	snp	A/T	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:20929725	ACATACAGAGTGGAA[A/T]AATAGACACTAGAGA	10529
rs143275311	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20879014	GACCACCTTCTAACC[C/T]GTGGCCTTTTGTGTG	10529
rs143282407	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20791684	ATGGGCGTGAGCACT[A/G]CACCATGCTAAGAAC	10529
rs143283705	snp	C/T	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21126669	AAAGAGACACACAAG[C/T]CAATTAGAAGAAGCC	10529
rs143305827	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21091057	ATGCCCCAAGGTCAA[C/T]TCCACCTCCTGAACC	10529
rs143314527	snp	A/C/T	0.0103295	0.0711199	intron-variant	NEBL	GRCh38.p7	10:20821252	ATCCCTTCACAAACA[A/C/T]GCTGTGTGCTTCACA	10529
rs143324240	snp	A/T	0.000798403	0.0199641	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21140524	ATGGATTAATGGGAA[A/T]ATAGTCTGTCCAGCC	10529
rs143332515	snp	C/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21072954	CGAGATCATGCCACT[C/G]TACAACAGCCTGGGC	10529
rs143339269	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20792841	CTGTCTAGTCCATGA[A/G]CAAGGTGGCTGTGCT	10529
rs143339289	snp	A/G	0.00835141	0.0640778	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21129275	TTTTTTAACTTTTTT[A/G]TTTTATTTTATTTTA	10529
rs143350888	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21063365	TTAATGCTCTAAGTT[A/C]CCAATTAATAGTTAA	10529
rs143351351	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20965572	GGACTGCAGAGAGTG[A/G]TCACACGGGGCTTTG	10529
rs143352732	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21034515	CAGGATAAGCCTCCT[G/T]GCAATACATAGACTC	10529
rs143355833	snp	A/G	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:21123388	AATTTGAGGATAATC[A/G]CTACTTCATATCTGT	10529
rs143355982	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21168236	ATGCCCTCAGGTAGC[A/G]ATTAAAATGAGAAAT	10529
rs143362547	snp	G/T	0.00874735	0.0655527	intron-variant	NEBL	GRCh38.p7	10:20887598	ATTTTTGTATTTTTG[G/T]TAGAGACCAGCTTTT	10529
rs143376693	snp	G/T	0.0158469	0.0875917	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20858850	TATATGTATTAAGTA[G/T]TGAATCTCCACAATA	10529
rs143378417	snp	A/T	0.0166325	0.0896639	intron-variant, downstream-variant-500B	NEBL	GRCh38.p7	10:20817332	AGATTGTGCCACTGC[A/T]TTCCAGTCTGGGTGA	10529
rs143379379	snp	A/C	0.000798403	0.0199641	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21135043	GGGCAACGTTTGTCC[A/C]GGTTCCAGTACACTC	10529
rs143391322	snp	G/T	0.079617	0.182947	intron-variant	NEBL	GRCh38.p7	10:21067022	GTGTTGCCCAGGCTG[G/T]AGTGCAGTGGCGCGA	10529
rs143393221	snp	G/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21026939	CCCACTCCCCCTCTT[G/T]GCCACCCATGGGCAC	10529
rs143403054	in-del	-/T	0.093777	0.195178	intron-variant	NEBL	GRCh38.p7	10:20832427	AATAAGTTATCTCTG[-/T]TTTTTTTTTTAAGCC	10529
rs143407130	snp	A/C	0.00953873	0.0683987	intron-variant	NEBL	GRCh38.p7	10:20956238	AGTAATCCTTATAGA[A/C]ATACTTTTCCCGAGG	10529
rs143418067	snp	A/C	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21164780	TATATACACTGGAAC[A/C]TTTTTATTGGCTCAA	10529
rs143421393	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21171828	CCGGTCTACTTCAGT[C/G]GGTCTACTACAAACG	10529
rs143427770	snp	C/T	0.00438332	0.0466095	intron-variant	NEBL	GRCh38.p7	10:21076393	GAGGTTGCAGTGAGC[C/T]GAGATCGTGCCACTG	10529
rs143459763	snp	C/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20885987	GTGAAACACTTAAAG[C/G]TGTTCTGCAAAGAAT	10529
rs143460330	snp	A/G	0.0107246	0.0724382	intron-variant	NEBL	GRCh38.p7	10:20912741	ACGTTGTGACTTGAG[A/G]TTTCTGAATGAATTA	10529
rs143468758	snp	G/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20827798	GGAGCTAGATGCCAT[G/T]ATACTTAGCAAACTA	10529
rs143471912	snp	G/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20822450	AGAAATAGGTATAGA[G/T]AAAAGAAATAGAAAA	10529
rs143483044	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21010888	CTTCCAATGTGAAAC[C/T]GATTTGCCCATCAAC	10529
rs143500335	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20910738	CCTATCTACTAATCA[A/C]CAGGGTACAAGGAAT	10529
rs143500746	snp	C/T	0.0252325	0.109451	intron-variant	NEBL	GRCh38.p7	10:20923099	TATGAGACAGGGTCT[C/T]GCTCTGTCACCCAGG	10529
rs143532917	snp	A/G	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21125419	ATTGGGGGTTGGGGA[A/G]AAGAAATGGGAAGTT	10529
rs143533039	snp	A/C	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21170149	CTACTTCAGTAGAAC[A/C]TTTTTCTGTCCTTTT	10529
rs143539623	snp	C/G	0.00557542	0.0525036	intron-variant	NEBL	GRCh38.p7	10:20912870	CTCATGGGGGCCATA[C/G]TATGCCAATTCTTTT	10529
rs143544310	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21015709	TAGAAACAGGAGTCT[A/C]CCTATGGCGCCCAGA	10529
rs143547042	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20947643	GTGCCAGGCTTTGCT[A/G]TTTACAAATCACAGC	10529
rs143554055	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20856324	AAAATAAAGGTCAAC[A/G]TTCTTGAAAAGCAAT	10529
rs143569091	snp	A/G	0.00182451	0.0301484	missense, intron-variant	C10orf113, NEBL	GRCh38.p7	10:21146388	CACAAGAAAAAAATG[A/G]CTGGTTGATTAGTAA	10529
rs143572248	snp	C/G	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20833146	TTGTTGTCTGCATAA[C/G]AAAACACACCAAAAC	10529
rs143581642	snp	G/T	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:20957570	TGTCTATAGACATTA[G/T]TCTATACTGATCTAG	10529
rs143584663	snp	A/G	0.0044037	0.0467168	intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20808617	CCGAAAGTACTGCTG[A/G]AATGGGATCGAGACC	10529
rs143595437	snp	A/G	0.00199481	0.0315187	intron-variant, downstream-variant-500B	NEBL	GRCh38.p7	10:20815558	TTTTCACAAGCAAAG[A/G]AGGACCGCAAGTAAA	10529
rs143599291	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21158510	ACCATTTTGTAGGTG[A/G]GGAAACCGAGGGATG	10529
rs143601092	snp	C/G	0.00914312	0.0669923	intron-variant	NEBL	GRCh38.p7	10:21166417	TACAACTCTCTAATG[C/G]GTAGCAGCCCATAGT	10529
rs143604286	snp	C/T	0.00279162	0.0372561	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20871941	TGTGTAAACAAAAAC[C/T]GGCTCTCAGGTGAAA	10529
rs143606020	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21109880	TTTATTGTGTCTATT[C/T]GATTCTTCTCTCTTA	10529
rs143615704	snp	C/T	0.00358779	0.0422022	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20782483	AGAAAAAGTCTTGTT[C/T]CTCATTCCCAGAGTG	10529
rs143616178	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21044727	CACCCTGCTCAAATG[C/T]CCCTGCTCCGTAAGC	10529
rs143619443	snp	A/G	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20975745	ATGTTAACCATTCAC[A/G]AGGTAACTACTGCCC	10529
rs143619572	snp	A/G	0.00993419	0.0697739	intron-variant	NEBL	GRCh38.p7	10:21116820	GACTACAGGTGTGCC[A/G]CACCAATCCCAGCAA	10529
rs143619885	in-del	-/TTAT	0.0205511	0.0992634	intron-variant	NEBL	GRCh38.p7	10:20997001	TCTATAAAATGTGGG[-/TTAT]TTATCCATAATCATA	10529
rs143627921	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21052361	AAGAAGCTAAGCTTT[C/G]CACCTCAATTCTCCA	10529
rs143631423	snp	A/G	0.00517822	0.0506191	intron-variant	NEBL	GRCh38.p7	10:20918231	GACATGGTGACAAGC[A/G]CTTGTAATCCCAGCT	10529
rs143644290	snp	C/G	0.000164859	0.00907756	intron-variant, missense, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20868666	ACTAAAGCCTTACTT[C/G]ACTAGAAAGTTTAGA	10529
rs143645819	snp	G/T	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:21013078	TATCCAGGGGTACAA[G/T]GGGGGCGTGGGGGCA	10529
rs143657852	snp	A/C	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21007560	TTTCATACATTATCA[A/C]CCTTATCATCTGACG	10529
rs143657973	snp	C/G	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:21048782	GGGTGGATCACCTTA[C/G]GTCAGGAGTACGAGA	10529
rs143667598	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21063807	CCCGGGAGGCGGAGC[C/T]TGTAGTGAGCCAAGG	10529
rs143670296	snp	A/T	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:20939781	AAAGGCAGGGGTTGC[A/T]ATCCTAGTCTCTGAT	10529
rs143679509	in-del	-/TCAG			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21132030	TTAAAATGTATAATT[-/TCAG]CAGTTTTAGTATATT	10529
rs143689693	snp	A/G	0.00795532	0.062565	intron-variant	NEBL	GRCh38.p7	10:20962881	AGAAAAGTTCACTTC[A/G]TTGAACATGGAATGG	10529
rs143690206	snp	A/G	0.0174175	0.0916809	intron-variant	NEBL	GRCh38.p7	10:21107770	CTTTGTACCTCTGGT[A/G]GAATTCAGCTGTGAA	10529
rs143690821	snp	C/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20905729	AAGACCCAGAGACAA[C/G]AGTTGAAAGAACCAA	10529
rs143700899	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20820135	AAATCCTGTACCTGA[A/G]CTTTAGTGATAGACT	10529
rs143702233	snp	C/T	1.64961e-05	0.00287189	stop-gained, intron-variant, utr-variant-3-prime	C10orf113, NEBL	GRCh38.p7	10:21126021	GCTGACTCTCCGCAG[C/T]CACCTGGCAAGCGTT	10529
rs143708503	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20914338	ACCTTAAAAGATACA[A/G]TGAACAAGATTTGCT	10529
rs143712487	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20876113	TAAATATTATTTTTC[C/T]GTAAGAGAATATAAG	10529
rs143715171	snp	A/G	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20808195	TCCTATGACTGTGTA[A/G]TGTGTATATTTATCA	10529
rs143721932	snp	A/G	0.00318978	0.0398085	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20872181	TGAAGAGAGGTGAAC[A/G]GCACAAAGGCAGCAG	10529
rs143734230	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21056292	TTCATAAAACCTAAT[A/G]TAGAGTACTTCAAAG	10529
rs143746354	snp	A/G	0.0115144	0.0749975	intron-variant	NEBL	GRCh38.p7	10:21106723	TCCAATTCTGTGAAG[A/G]AAGTCAGTAGTAGCT	10529
rs143766851	snp	C/G	0.00795532	0.062565	intron-variant	NEBL	GRCh38.p7	10:21068493	GGGGGGAGGAACATT[C/G]TTTCCCCTGAGATGG	10529
rs143767029	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21096238	CTCGTCCTTCCCTCT[C/T]TCTTCCCACTGTCCT	10529
rs143770179	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21002259	AAGTTATTCCTAAAT[A/T]ATTGTAGCAGAACTT	10529
rs143772876	snp	C/G	0.0232847	0.105357	intron-variant	NEBL	GRCh38.p7	10:21149510	TGGCCAGGCTTGTCT[C/G]AAACTCCAGACCTCA	10529
rs143780161	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21047208	CAGCTTGTTGATTTA[A/C]TCAAGAACAAAAATA	10529
rs143782776	snp	C/G/T	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:20903299	TCAGATAAATGCAAA[C/G/T]TAAAACCACAATAAG	10529
rs143784635	snp	C/T	0.00795532	0.062565	intron-variant	NEBL	GRCh38.p7	10:21110970	AAATAGGGAGCCAAA[C/T]CATGAGTGAACTCCC	10529
rs143790393	snp	C/G	0.00279162	0.0372561	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20858092	TGGGATTTCTGCAAG[C/G]AGAGGACTGTTTTTC	10529
rs143798071	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20803157	TTTATCATGTAAATT[A/G]CAGCTAGACAGGAGA	10529
rs143800767	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20909137	CTCAAGCATTTATCG[C/T]TTGAGTTACAAACAT	10529
rs143814949	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21009665	TCAGAATACAATACA[A/G]TTGTCCCAAACGGAA	10529
rs143816983	snp	C/G	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:21050056	GGGGGAGGAAGACTA[C/G]GTAATATCTAAGGTC	10529
rs143822902	snp	C/T	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:21115188	TGACACTTTTTCCCT[C/T]TTGCCCCTTCCTGGC	10529
rs143826889	in-del	-/A	0.02016	0.0983543	intron-variant	NEBL	GRCh38.p7	10:21057018	AATAAAGTATTATTT[-/A]AAAAAAACAGGTAGA	10529
rs143836320	snp	A/G	0.00953873	0.0683987	intron-variant	NEBL	GRCh38.p7	10:20806074	ACATTTTCTCATTCA[A/G]TTTGGCTTAGGATAG	10529
rs143856552	snp	A/G	0.00398564	0.0444627	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21145923	TCTGGACCGCAGCTC[A/G]GGCCCATTGGGCATC	10529
rs143874524	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21033132	GGAAATGTGTGACAT[C/T]GAGCAGCCCTGTGAT	10529
rs143886727	snp	A/C	0.000798403	0.0199641	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20873113	ATCTGACATTTCTCA[A/C]TAAGTATTTGCTCCA	10529
rs143892258	snp	C/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20806907	TAACATTAAATAAGG[C/T]TGATCAACATTAGTT	10529
rs143895735	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20993441	CCACAATTATACTGC[A/G]TAGCAAACTAGCCCA	10529
rs143901451	in-del	-/G	0.00914312	0.0669923	intron-variant	NEBL	GRCh38.p7	10:20810378	ACAAACAAAAAAAAA[-/G]TCCCTTTCTATAACA	10529
rs143906130	snp	C/T	0.031825	0.122064	intron-variant	NEBL	GRCh38.p7	10:20896018	GTTGACTTTGGAGGA[C/T]GTGCCAGACCACTAC	10529
rs143921441	snp	C/T	0.00636936	0.0560724	intron-variant	NEBL	GRCh38.p7	10:20900551	GGCATGGGCTGGGTG[C/T]GGTGGTTCACGCCTG	10529
rs143926096	snp	C/T	0.00953873	0.0683987	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20856359	CATAGGAGTGGCACG[C/T]TTTCTTCCAGCCACC	10529
rs143930021	snp	C/T	0.00217567	0.0329105	missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20812805	TGTCCATCTCCACGA[C/T]GTGAGGGTGGACCCC	10529
rs143939431	snp	A/G	0.00874735	0.0655527	intron-variant	NEBL	GRCh38.p7	10:20792530	GTCCTGGCCGGGCAT[A/G]GTGGCTCACGCCTGT	10529
rs143950311	snp	C/G	0.00517822	0.0506191	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21128705	TCATCAACACCTTTT[C/G]CAAATCTCAACTCTC	10529
rs143953771	snp	A/C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21152322	TAATATTTTAAATCC[A/C/G]TTAGTCCCAAGAATT	10529
rs143957419	snp	C/T	0.00795532	0.062565	intron-variant	NEBL	GRCh38.p7	10:20804735	GTGAGAGTGGACAGA[C/T]ATACTTGGAATGGCA	10529
rs143962290	snp	C/T	9.89772e-05	0.00703412	intron-variant, synonymous-codon, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20869806	AAGTTCTGCACTGTA[C/T]GTGTGGGTGTCCTGC	10529
rs143964236	in-del	-/TTG	0.0741063	0.177655	intron-variant	NEBL	GRCh38.p7	10:20819714	CCTTGTCAAGTGGTT[-/TTG]TTGTTGTTGTTGTTG	10529
rs143978719	in-del	-/T	0.116138	0.211142	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20861060	AAAAGAAAAACTGAC[-/T]TTTTTTTATTATTTT	10529
rs143983323	snp	A/G	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:21029460	CCTGCTCAGTGCCCT[A/G]AGTCTCAATTAAGAG	10529
rs143985714	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20955532	AGAAATCGAAGAACA[C/G]AGGTGAAAAGTAGTG	10529
rs143987423	snp	C/T	0.0310518	0.120672	intron-variant	NEBL	GRCh38.p7	10:21097383	AGAATCACTTGAACC[C/T]GGGAGGTGGAGGTTG	10529
rs143991504	snp	A/G	0.00478085	0.0486577	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21142559	CAAAATGAGCATCTA[A/G]GGGAAATTGTGGGAT	10529
rs143995648	snp	C/T	0.0138799	0.0821421	upstream-variant-2KB, intron-variant	C10orf113, NEBL	GRCh38.p7	10:21148248	TATACTCCTGTGATA[C/T]TATGAAACATGTACA	10529
rs143998663	in-del	-/A	0.030665	0.119967	upstream-variant-2KB, intron-variant	C10orf113, NEBL	GRCh38.p7	10:21146720	ATGCCCTGGTAAAGT[-/A]AAAAATTTTTTTTAA	10529
rs144005068	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20796358	AGAGTGAAACTCAGT[C/T]TAAAACAAGAAAAAA	10529
rs144006037	snp	A/G	0.00358779	0.0422022	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20958689	CCCAGCCATTTAGTC[A/G]ATTCTGAAATACTGC	10529
rs144009531	snp	C/T	0.0197687	0.0974348	intron-variant	NEBL	GRCh38.p7	10:21074697	GTTAGCCAGGATGAT[C/T]TTGATCTCCTGACCT	10529
rs144014129	snp	C/T	0.00597247	0.0543191	intron-variant	NEBL	GRCh38.p7	10:20904233	TTCTTGGGAAGGCAA[C/T]TGAGTACTGTCCATG	10529
rs144015045	snp	C/T	0.00517822	0.0506191	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20870417	ATCTTAAAGGGTCTT[C/T]GTATCTACCACTTTA	10529
rs144018464	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20996195	ATGTGCCACTACGAT[A/G]TGATACGCTTTCAAG	10529
rs144021408	snp	A/C	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:21062845	TGGAAGGTAACAATG[A/C]TGTGATATCAATTTT	10529
rs144023135	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21032938	CCTGACCTACCCTAC[C/T]ATGAAATGCTTATCG	10529
rs144024787	snp	A/G/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20989733	ATGACCATTATATCT[A/G/T]AGGGATTCTTGTTCC	10529
rs144045282	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20927820	TATGTTTCCTAAACT[A/G]TTTCTGCTTCTCGTG	10529
rs144048184	snp	A/C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20901685	TAGGTGAAAGAAGAA[A/C/T]TTGTTTGCCTGATTT	10529
rs144053702	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21092883	AGCCTGTCCATCAGA[G/T]ACCCATGCCAAGCAA	10529
rs144055823	snp	A/G	0.00398564	0.0444627	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21133945	ATTCTTAAAAGGGCC[A/G]GGCACAGTGGCTTAC	10529
rs144058895	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20967691	CTTGATAACAACTTT[C/T]AGGGGAGTGGTGACA	10529
rs144066723	snp	G/T	0.00993419	0.0697739	intron-variant	NEBL	GRCh38.p7	10:20889662	ATGAAGCATACATAG[G/T]AAAATCTGTCAATCT	10529
rs144089900	snp	C/G	0.00835141	0.0640778	intron-variant	NEBL	GRCh38.p7	10:21098871	TGGCGGCTCACACCT[C/G]TAATCTCATAATCCC	10529
rs144092569	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20855746	AACTTTAATTAGAAT[G/T]ATTTTACACAGTAAT	10529
rs144099209	in-del	-/CTT	0.0189856	0.0955633	intron-variant	NEBL	GRCh38.p7	10:20811580	AACATGTTTGGAATC[-/CTT]CTTCAGAAAATACTT	10529
rs144112897	snp	A/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20797382	CCCTTAGACAATACC[A/T]TCAATCCATAAGGAG	10529
rs144113605	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20991978	CTGTGTACCATTCCA[C/T]GGTGTATGTGTACCA	10529
rs144139914	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20857076	TCAGGTGATCCACCC[A/G]CCTCCCACAGTGCTG	10529
rs144147330	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20793269	AAGACATGCCTAATC[A/T]TCGTGATACAAAATA	10529
rs144180595	snp	A/G	0.00874735	0.0655527	intron-variant	NEBL	GRCh38.p7	10:20791382	AGAAGATGAAAAGGG[A/G]GGAAGAAAAGTTTTG	10529
rs144182130	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21018908	TAGCAGGCGCCTGTA[A/C]TCCCAGCTATTGGGG	10529
rs144188474	snp	C/T	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:21084142	GTCCCAGATTGGGTA[C/T]TAAATTCTGCAGTCC	10529
rs144206569	snp	A/C	0.00279162	0.0372561	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21130951	AAATGTCAATGAAAC[A/C]AAAAACTGGTCCTTT	10529
rs144217055	snp	A/G/T	0.0047834	0.0487097	intron-variant	NEBL	GRCh38.p7	10:21012352	TGATTGTGTATATAT[A/G/T]TATTTATTTATTTAT	10529
rs144218105	snp	C/T	0.00795532	0.062565	intron-variant	NEBL	GRCh38.p7	10:21077903	CACTATTCATGACCA[C/T]GAGAAAGTACTTTAG	10529
rs144220385	snp	A/C	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20983201	AAATTAGATAATCTC[A/C]ATAAGTCTTGTAGAA	10529
rs144220803	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21021889	TGTGGACAGAAGAAA[C/T]GAAGGGATGGAGGGA	10529
rs144222666	snp	A/C	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:21088523	GCCCAGAAGTGACAC[A/C]CATCACTCTGACCTT	10529
rs144229798	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20924804	AACGGTCGTTCAGTT[C/G]CAGGTCAGCCCAGAA	10529
rs144231628	snp	A/C	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:20944534	ACTAATGTAGCATTT[A/C]TCTCTATATTTGTAT	10529
rs144233596	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20890315	GCCTTGACACATAAG[A/C]CTTTGGCCAAACAGA	10529
rs144233701	snp	A/G	0.0123036	0.0774623	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20854776	CACTACGCTGCCCAC[A/G]CTGGTCTCAAACTCC	10529
rs144249479	snp	C/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20892537	TTGTGTTAGAGTTTT[C/G]CTGTTTTTACAGTCA	10529
rs144251710	snp	A/G	0.0748431	0.178382	intron-variant	NEBL	GRCh38.p7	10:21046894	GGCATGAGCCACCGC[A/G]CCCGGCCCCTAACCT	10529
rs144252404	snp	A/T	0.0178098	0.0926698	intron-variant	NEBL	GRCh38.p7	10:20829077	CATTTAATCAACCTG[A/T]CAAGCAGATACTATT	10529
rs144262167	snp	C/T	0.0368353	0.130617	intron-variant	NEBL	GRCh38.p7	10:20976320	GCACTCCAGCCTGGG[C/T]GACTGAGACTCTATA	10529
rs144280648	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21171351	AAAAAAAAAAAAAAG[A/G]AAAAAAAAAAAGAAA	10529
rs144291846	snp	G/T	0.00358779	0.0422022	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20881756	ATTTGTTCAGTGAAT[G/T]AATAAATAAATAAGT	10529
rs144297434	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20780859	TTGCCGTCATTTAAG[C/T]AGTTTCAATAGATAA	10529
rs144300228	snp	C/T	0.0209421	0.100162	intron-variant	NEBL	GRCh38.p7	10:20942119	GAACCAAAAAAGAGC[C/T]CACCTTGCCAAGTCA	10529
rs144302275	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20886987	AGACCAGAGCAAGGA[A/G]CGAGACAGATGAGGT	10529
rs144305061	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21114328	AATTGATTAAGATTT[G/T]TTTTATGGCCCAAAA	10529
rs144306003	snp	C/T	0.00835141	0.0640778	intron-variant	NEBL	GRCh38.p7	10:21025336	AAGAATTGGCTGAAG[C/T]GTGTGTATCAAGACT	10529
rs144336187	snp	A/G	0.0232847	0.105357	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20785177	AGCCTAGGGAACAAG[A/G]AAATTTCTCTGTTTA	10529
rs144337477	snp	C/T	0.00398564	0.0444627	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20872872	CATGAATAATCCACC[C/T]CTTGTTTAGCATATC	10529
rs144346263	in-del	-/AAT	0.0414363	0.137845	intron-variant	NEBL	GRCh38.p7	10:21005734	CAAGTGTCTCAAAAC[-/AAT]AATAATAATAATAAA	10529
rs144352590	snp	C/G	0.00716266	0.059414	intron-variant	NEBL	GRCh38.p7	10:21119247	CATCTCTAACACAAA[C/G]TTCTTTCTTCCTAAC	10529
rs144357111	snp	A/G	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20835789	TTCTGAACTGCTTAG[A/G]ATGATAATCTCATTC	10529
rs144361238	in-del	-/TA			intron-variant	NEBL	GRCh38.p7	10:20789954	ATATATATGTGTGTG[-/TA]TATATATATATATAC	10529
rs144364627	snp	C/T	0.00636936	0.0560724	upstream-variant-2KB, intron-variant	C10orf113, NEBL	GRCh38.p7	10:21147294	TCAAAAACTAGGAAC[C/T]TTCGCCCAGTTTCTC	10529
rs144367294	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20958591	CTGAATATTAATATA[C/T]TCAATGAGATGAAGA	10529
rs144377750	snp	C/T	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:21160270	CTGGGCAGCAGCCCC[C/T]GTGTGCAAATCTTGA	10529
rs144385619	snp	C/T	0.00318978	0.0398085	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21134001	GGAGGCTGAGGTAGG[C/T]GGATCACTGGATGTC	10529
rs144398669	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20784814	TTCAAAACTAGAGTG[C/T]GATGCAGCAGGAAAA	10529
rs144399350	snp	A/G	0.0146672	0.084371	intron-variant	NEBL	GRCh38.p7	10:21118747	TTACATATGTGCGAA[A/G]TGAGTCTTAATAAAG	10529
rs144402571	snp	C/T	8.23825e-05	0.00641751	intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20835596	CTTTCCCTTTAATTA[C/T]TGACTCCAGGTCTTT	10529
rs144415419	snp	A/G	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21041310	GAACATGCGGTATTT[A/G]GTTTTCTGTTCCAGC	10529
rs144424778	snp	A/C	0.016652	0.0898765	intron-variant	NEBL	GRCh38.p7	10:21082634	TTCCTCACCTAATTC[A/C]GATGCCCATTTTGAT	10529
rs144463910	snp	C/T	0.0240643	0.107019	intron-variant, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20880102	GCACGGTGGCTCGTG[C/T]CTGTAATCCCAGCAC	10529
rs144469430	snp	C/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20907166	AAACCTTTAAAATTA[C/T]ATTTAAGATAATGAT	10529
rs144485241	snp	C/T	0.00755907	0.0610114	intron-variant	NEBL	GRCh38.p7	10:21165800	GGAAAGGTGTGGGGT[C/T]GGGTGTGATGGGCAC	10529
rs144485769	snp	C/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20965123	TCCTTTGCTCATTCA[C/G]CAAATCTTTACTGAG	10529
rs144485812	snp	C/T	0.0189856	0.0955633	intron-variant	NEBL	GRCh38.p7	10:21008802	AGGTTCGGTACTATC[C/T]GCAGTTTTCAGACAT	10529
rs144486044	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20907725	TAAAAGAAATTTAAA[A/C]ATTTTCAAGTGTTCA	10529
rs144489225	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20839211	TGCCGCCATCCTGCC[A/G]TTCAACTGCATCTGT	10529
rs144500561	in-del	-/CAGA	0.0287284	0.116357	intron-variant	NEBL	GRCh38.p7	10:21117825	AACAGGCTCTAGAGT[-/CAGA]CAAACTGGGTTCAAG	10529
rs144516463	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20964755	TGCTGACTACCATGT[A/G]GCCACTGTCCAATAA	10529
rs144525190	snp	C/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20967939	ACTGAGGAACCCAGA[C/G]ATTAGACAAAAAACA	10529
rs144525309	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20878135	AGAAAACTCTTGCCC[A/G]GGAACTCCATTACTC	10529
rs144525483	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20911072	GGGAGGATGAAGTGG[A/G]AGAATTGCTTGAGCC	10529
rs144532549	snp	G/T	0.0287284	0.116357	intron-variant	NEBL	GRCh38.p7	10:21107690	AGCCTCATAAAATGA[G/T]TTAGGGAGGATTCCC	10529
rs144535136	snp	A/G	0.0126979	0.078662	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21144014	TGAAAACTCCAACAA[A/G]GAGAGAAGGATTTTT	10529
rs144538235	in-del	-/C			intron-variant	NEBL	GRCh38.p7	10:21029742	GGCCCATGCCGGGAT[-/C]ATGGATCGATATGGC	10529
rs144544054	in-del	-/CCCCCCCC			intron-variant	NEBL	GRCh38.p7	10:21118115	TGGTGCAGCACCCCA[-/CCCCCCCC]CAGCCACTACCAATG	10529
rs144549976	snp	A/G	0.00874735	0.0655527	intron-variant	NEBL	GRCh38.p7	10:21003626	TGACTGAGGGATGAC[A/G]TCATGAGTTTCTTGA	10529
rs144552860	snp	A/G	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:21070337	TATGCTTTAATCACT[A/G]TCAGATTGCCCTGGT	10529
rs144564894	snp	A/G	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:20917218	GTCCTCACCCAGCAT[A/G]CACACAAACACAAAA	10529
rs144565313	snp	A/G	0.0119091	0.0762411	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20860906	AGAGAAAATCTTGGT[A/G]GGAATACAGCATTTG	10529
rs144603604	snp	C/T	0.367297	0.220775	intron-variant	NEBL	GRCh38.p7	10:21108116	TTCAAAAAAACAGCT[C/T]CTGGATTCAATGATT	10529
rs144638436	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20926053	AAAGAACATTTTGTT[C/T]AACTAAACTCTCCAT	10529
rs144640791	snp	A/G	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21072453	ATTCAGCCACTACAT[A/G]AGAGGTGCCACTTTT	10529
rs144650437	snp	C/G	0.00755907	0.0610114	intron-variant	NEBL	GRCh38.p7	10:21004137	GTTGATTTTTTTAAA[C/G]CATTCTAGCCTTTAA	10529
rs144653401	snp	C/T	0.00398564	0.0444627	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20870796	CATGTTAGACACAAA[C/T]CAAAGTATGGTAAGT	10529
rs144654262	snp	A/G	0.00438332	0.0466095	intron-variant	NEBL	GRCh38.p7	10:21110249	ATACTTTTTCCTTCA[A/G]TCTTTGTTAGAACTC	10529
rs144659321	snp	C/T	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:21045366	ACAATCTCAATCTCG[C/T]GATACTAACTGCTAA	10529
rs144677239	snp	G/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20895900	ATTCAGCATTTATAT[G/T]CATTACCATTATTTA	10529
rs144679169	snp	A/G	0.0189856	0.0955633	intron-variant	NEBL	GRCh38.p7	10:21008855	TTCCCTGCAAATAAG[A/G]GGTGTCTACTGTATG	10529
rs144687319	snp	A/G	0.0244538	0.107838	intron-variant	NEBL	GRCh38.p7	10:20941249	CACCATGATCAAGTG[A/G]GCTTCATCCCTGGGA	10529
rs144688785	snp	A/G	0.00113449	0.0237899	intron-variant	NEBL	GRCh38.p7	10:20831355	TTAAGCTTTAATAGC[A/G]ATGTTGAAATTTACA	10529
rs144697584	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20864189	CAAGTAACAAGATGA[C/T]CTATGGATATATTAA	10529
rs144700461	snp	A/G	0.00795532	0.062565	intron-variant	NEBL	GRCh38.p7	10:21107396	CTGTTGAATTTTGTC[A/G]GAGGCCTTTTCTGCA	10529
rs144702224	snp	A/C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20800395	GCATTTAAGTTGTTT[A/C/T]CATATCTTGGCTATT	10529
rs144703350	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20869323	TACGCCATGTAGGAA[C/G]TGGACAAAGGTAAGT	10529
rs144705759	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20826665	CTATTTATGAGTGCC[A/G]GAATTATAGGAACAA	10529
rs144748059	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	NEBL	GRCh38.p7	10:21175707	AGTCCACCTCAAAAG[A/C]AAATAAAATGAGAAT	10529
rs144753129	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21022887	AAATACCAGAGTTAT[A/T]GATTCAAACGAGTAA	10529
rs144755790	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20989517	ATGCAGTAATTTATA[C/T]GGATGAATAAACAAC	10529
rs144765263	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20953576	CCCTATGATATATTA[A/G]GATAGGGGAAGTCCT	10529
rs144770461	snp	C/T	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:21105823	GTAAAAGCGTTCCTA[C/T]TTCTCTACATCCTCT	10529
rs144772303	snp	C/T	0.00716266	0.059414	intron-variant	NEBL	GRCh38.p7	10:21050189	AGTCTCTCTTTTGCC[C/T]GGACATCATTAGATA	10529
rs144805063	snp	C/T	0.29278	0.246313	intron-variant	NEBL	GRCh38.p7	10:20923661	TCCAGAGCAAGACTC[C/T]GTCTCAAAAAAAAAA	10529
rs144807780	snp	C/T	0.0107246	0.0724382	intron-variant	NEBL	GRCh38.p7	10:20803846	ATATATATGCACACA[C/T]ACTGGGAATGTTTTC	10529
rs144811221	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21021367	AGTAAAACCTTTCAA[C/T]GGCTTCCAGTTGATC	10529
rs144814190	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20932740	AACCATTTTATTTGT[C/T]GATACTAATCGTTGT	10529
rs144815863	snp	A/G	0.000247572	0.0111232	intron-variant, synonymous-codon, nc-transcript-variant	NEBL	GRCh38.p7	10:20813978	TTTAACATGTCTCAT[A/G]GCAGGTGTATCTAAA	10529
rs144824535	snp	A/G	0.00557542	0.0525036	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20867437	AGTATTTTCAAAGTC[A/G]AAAAAACTATAAATG	10529
rs144841635	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20838947	CATAACATGTATATG[C/T]ATGGAGAAACCAAAA	10529
rs144848590	snp	A/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21156632	CCATTACTTATATAT[A/T]AAAAATGGCAATTAC	10529
rs144859899	snp	C/G	0.0107246	0.0724382	intron-variant	NEBL	GRCh38.p7	10:21088109	TCCATCAGGAATCAC[C/G]CCTGGGTCTACATTC	10529
rs144861051	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20994225	AGTCATTTATTTTAT[A/G]TCATACTTAATTGCT	10529
rs144865823	snp	A/G	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:20922096	TTGTATGGACACTGT[A/G]TGACAGAGCAAAAAC	10529
rs144871465	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20865688	AGAGCTTAGAGTCAC[C/T]GCCCTTTAATGCAAG	10529
rs144872222	snp	C/T	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:21079346	AGCACAAATCTTTGG[C/T]AGGCTCTCATTTCTG	10529
rs144874496	snp	A/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20985281	CTGTAATGCCCTTCA[A/T]TCTCAAACAGATCAC	10529
rs144880561	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20925968	AGGTGTGGGCCATTC[A/G]TAAACAGGTGTCCAT	10529
rs144889805	snp	G/T	0.00676609	0.0577691	intron-variant, upstream-variant-2KB	NEBL, LOC102725112	GRCh38.p7	10:20843644	AATAATTATTAAACA[G/T]TTTTCTTCCAAAAAG	10529
rs144900822	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20893627	TGCAGGCTTCCTAGG[G/T]CTGATCTCTAGGCCA	10529
rs144916093	snp	C/T	0.00755907	0.0610114	upstream-variant-2KB, intron-variant	C10orf113, NEBL	GRCh38.p7	10:21148278	ATTGGTTTCCATCCA[C/T]GTTCATGGCTCATCA	10529
rs144921744	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21059976	ATTTGATACAATAGC[A/T]TTGGGGTACTGAGAC	10529
rs144925755	snp	C/T	0.0107246	0.0724382	intron-variant	NEBL	GRCh38.p7	10:21020282	CATTGTTTTGCACAT[C/T]CCCCCTTTTCCCAAC	10529
rs144946187	snp	A/G	0.000445306	0.0149149	utr-variant-3-prime, synonymous-codon, nc-transcript-variant	NEBL	GRCh38.p7	10:20785828	GTACATCCAGCCATC[A/G]TCAATAGGCTGCACG	10529
rs144959952	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21163189	TGAAAGGCTCTGAAA[C/G]TCTGCTAGAAACCCA	10529
rs144960266	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21118128	CCACAGCCACTACCA[A/G]TGAAAACTACAGCCT	10529
rs144962641	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21026576	ATCTTCTCCCTCCTG[A/G]GCACTTAAGTCCACC	10529
rs144992348	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20875075	AATCTGTTCTTTGTT[A/G]CTTCCAACGAATATT	10529
rs144993622	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21054999	CAGAACTGATGAAAG[A/T]TCTGTTTCTGTTAAG	10529
rs145002876	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21051234	TATATTCGGAGATCA[C/T]ATTTTTTATTGTAAT	10529
rs145015123	in-del	-/TAAT	0.149999	0.229128	intron-variant	NEBL	GRCh38.p7	10:20975923	TGAGAAACTTAAACC[-/TAAT]TAATCAGAGGCCCTA	10529
rs145025995	snp	C/T	0.000153988	0.00877328	intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20889942	TTAAACTCTTCTTTA[C/T]AACGGATCTAAAAAA	10529
rs145041113	snp	A/C/T	0.0205511	0.0992634	intron-variant	NEBL	GRCh38.p7	10:20911662	TAAGTGGATTTTATA[A/C/T]GTACATAAAATAGGG	10529
rs145041513	snp	A/G	0.0228947	0.104514	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20855070	CTCTACTACAAATAC[A/G]AAATTAGCTGGGAGT	10529
rs145044486	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20812111	GGAGTACCATCAGAA[C/T]GCCCATGGCGTGTCT	10529
rs145049147	snp	C/T	0.00953873	0.0683987	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20882535	ATCCTGTGCCTAACA[C/T]AGTGAATGACAGAGT	10529
rs145074212	snp	C/G	0.0111196	0.0737302	intron-variant	NEBL	GRCh38.p7	10:21159114	ATGCTTTTCCTCCAC[C/G]CTTTTTTTAAAGATG	10529
rs145077579	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20796394	AAAAAAAAAAAAAAA[A/C]CTTCTCTAAAATATT	10529
rs145081507	snp	A/G	0.00636936	0.0560724	intron-variant	NEBL	GRCh38.p7	10:21067683	AGAGAACACCTTCCT[A/G]TTAAAATGGAATACA	10529
rs145086068	snp	C/G/T	4.94265e-05	0.00497104	intron-variant, synonymous-codon, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20819457	GTTTCGCCTCACTCT[C/G/T]TCTATCTCCGGGGTC	10529
rs145093887	in-del	-/AAATAT			intron-variant	NEBL	GRCh38.p7	10:21061562	ACATATATAAATATA[-/AAATAT]AATATAAATAGCATT	10529
rs145098713	snp	A/T	0.00795532	0.062565	intron-variant	NEBL	GRCh38.p7	10:21004907	ATCTCACCTTTCTTT[A/T]TCCTCTAAAACCCTT	10529
rs145116659	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21119589	CATACATGTTTTAGA[A/T]AATTTACATGTATAA	10529
rs145118763	snp	A/G	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:21031508	GCAGCAACTTCAGGC[A/G]GAAACATGAACTGGT	10529
rs145119675	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20810403	ATAACAGAAATGAAT[A/G]TTTAAAATGTGGAAT	10529
rs145121729	snp	A/C	0.00100387	0.0223814	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20852690	CTTAGAATCAAAGAG[A/C]CTGATTAGAGCAATA	10529
rs145129141	snp	A/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20908701	GGAGTCGGGAAGAGA[A/T]GAACACACTCTGCTC	10529
rs145134919	snp	A/C	0.0107246	0.0724382	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20960503	TGTCCATTTAAAGAG[A/C]AAAAAACAATGTGTA	10529
rs145141524	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20937465	GCCAGGGGGTGGAGA[C/T]AAGATGGTCGAATAG	10529
rs145160547	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20812637	TAATACTTTACCTGC[A/G]GTCCATTTTAAATTG	10529
rs145160550	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21157264	TTGAGGTGTCATTGA[A/T]ATACAAAAAATTAAC	10529
rs145172559	snp	G/T	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:21088906	CTGGAAGAACTGCCC[G/T]CTGCCGTGAGGATGG	10529
rs145185081	snp	C/G	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:21041911	TCATGGTGCTGGTGG[C/G]AGTGTCTTTTAGCAT	10529
rs145188546	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20849614	GTCTTTCCACCTTCT[C/G]CCATGGGATGATTCA	10529
rs145208891	snp	C/T	0.00636936	0.0560724	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21144364	TTCAACCATCCAAAT[C/T]GCCCTACAAGGTAAC	10529
rs145215398	snp	C/T	0.0111196	0.0737302	upstream-variant-2KB, nc-transcript-variant	NEBL, NEBL-AS1	GRCh38.p7	10:21174811	AGAGCCTTCTCTCAC[C/T]GGCTCCCAGACCCCG	10529
rs145221267	snp	A/C	1.64961e-05	0.00287189	intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20888157	TGTGGCTGGCATCCG[A/C]TTATAAAGAGAATTA	10529
rs145224776	snp	C/T	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:21003683	TGTGAAGCTAAAAGG[C/T]TCTCAGGCAGGATCT	10529
rs145229341	snp	A/T	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:21167662	ATACACACAACAAAT[A/T]AAATAATTTATTTGA	10529
rs145229370	snp	A/C	0.00149658	0.0273139	intron-variant	NEBL	GRCh38.p7	10:20823329	AAGAATATAACGTTA[A/C]CTTTATTCTATGCAA	10529
rs145236275	in-del	-/T			intron-variant	NEBL	GRCh38.p7	10:21033227	CTCGAGTATCTAAGA[-/T]TATGAGTATACTCTG	10529
rs145243777	snp	C/T	0.0402882	0.136092	intron-variant	NEBL	GRCh38.p7	10:21004667	GGAGCTTGCAGTGAG[C/T]CGAGATTGCACCACT	10529
rs145246977	snp	C/G	0.00517822	0.0506191	intron-variant	NEBL	GRCh38.p7	10:21072894	TACTTGGGAGGCTGA[C/G]GCATGAGAATTGCTT	10529
rs145256556	snp	C/T	0.0178098	0.0926698	intron-variant	NEBL	GRCh38.p7	10:21107159	TTCCTCTTTTCCTAA[C/T]TGAATACCCTTTATT	10529
rs145265253	snp	C/G	0.0103295	0.0711199	intron-variant	NEBL	GRCh38.p7	10:20907516	CAAATAGTGAAATAT[C/G]TTCCATCGATACTCC	10529
rs145269711	snp	A/G	0.000153988	0.00877328	intron-variant, missense, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20859751	GCTGATTCTGCCTAA[A/G]AGAAGCACTTTCAAG	10529
rs145272030	snp	A/G	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:21001729	CTGCTCAAGGTCATC[A/G]CCAAGGTCTGATTGC	10529
rs145273435	snp	A/G	0.00993419	0.0697739	intron-variant	NEBL	GRCh38.p7	10:20965315	AGAGAGAAAAATAGC[A/G]AGACAAGGGGACGTG	10529
rs145276859	snp	C/G	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20936694	TAAATAAATAATGCA[C/G]TGTTTTCTGTGTTTC	10529
rs145311587	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21017984	CGCCACCACTCCCAG[C/T]TAATTTTTGTATTTT	10529
rs145314639	snp	C/G	0.0232847	0.105357	intron-variant	NEBL	GRCh38.p7	10:20952984	TAGCTCATGATAGCA[C/G]CTTATATTATAATTA	10529
rs145320707	snp	C/T			intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20898702	CTTCAACCAAAAAAC[C/T]TGCTTAGGCTTGCTT	10529
rs145325199	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20799684	TAGCAAGGAGTTGGA[C/T]TGGGGAGTGATCTTG	10529
rs145338854	snp	G/T	0.0138799	0.0821421	intron-variant	NEBL	GRCh38.p7	10:21034064	CTCAGCTACTAGGGG[G/T]GCTGAGGTGGAAGGA	10529
rs145340865	snp	A/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21103821	TATCCATTTTTTTCA[A/T]TTATAGTTATACTTT	10529
rs145342662	snp	A/G	0.00159617	0.0282053	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21142797	TGAGGGATCCCAGTT[A/G]TGCTCCTTATGAGAA	10529
rs145359432	snp	C/T	0.00358779	0.0422022	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20866876	GAATTATCTATTTCA[C/T]TGACCCCTTTTTCTA	10529
rs145362453	snp	G/T	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:21036525	GGAAGACCCCTTAGT[G/T]GATAGTCAATGAATA	10529
rs145381143	snp	C/T	0.00318978	0.0398085	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21142027	AACATCAACTCCAGC[C/T]TGGCCGGGATTAAAG	10529
rs145388124	in-del	-/TTC	0.0146672	0.084371	upstream-variant-2KB, intron-variant	C10orf113, NEBL	GRCh38.p7	10:21147369	TGTATCTTTCTGGAA[-/TTC]TTCTCTGACCCTGTT	10529
rs145401829	snp	A/C	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:21010408	TGCTACCATGCCCAG[A/C]GAATTTTTTAATTTT	10529
rs145410692	snp	A/G	0.000132059	0.00812478	missense, intron-variant	C10orf113, NEBL	GRCh38.p7	10:21146468	GAAATTTCAGGTGCC[A/G]TGCTTTCCATAGAGT	10529
rs145435685	snp	A/G	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:21048330	ATGCTGGGGAAACAC[A/G]GCTGGAAAACATGTA	10529
rs145439466	snp	A/G	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21111373	AGTAAAAACAGGCTG[A/G]TACTGGTACCAAAAC	10529
rs145441867	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20798447	ATGACTCTACTGTTT[C/T]GCACATGAGACAGAC	10529
rs145442025	snp	A/T	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:20835702	TGATACTAAAAAAAA[A/T]ATAGTTAGACATATT	10529
rs145447223	snp	C/T	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:20987145	TGCATATGTACTATC[C/T]GTACCGACCGTTATG	10529
rs145449809	snp	A/G	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20952816	ACACTGAGGCACGAG[A/G]ATTACTTGAACCCCG	10529
rs145454831	snp	A/T	0.00597247	0.0543191	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20877297	GGAGATTTAGAGACA[A/T]TAAGTAACTCATCCA	10529
rs145475198	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20800808	AGGAGTCAATTTCTT[A/G]GTAAAAATCTAAACA	10529
rs145513363	snp	A/C	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20810200	CACACAACACAGGAG[A/C]ACATGGGGCAGCTAT	10529
rs145514868	snp	A/C/G	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:21027468	GAGTAGCTGGGACCA[A/C/G]AGGCAACTGCCACCA	10529
rs145516886	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20982465	TTTAAAAGTACACTA[C/T]AATATCACTAAAATG	10529
rs145524892	snp	C/G	0.00438332	0.0466095	intron-variant	NEBL	GRCh38.p7	10:21154395	ACCTGGGAGGTGGAG[C/G]TTGCAATGAGCTGAA	10529
rs145531679	snp	A/G/T	0.0138882	0.0821658	intron-variant	NEBL	GRCh38.p7	10:21057997	TCTGACTTTCCATCT[A/G/T]TTTTTTCTGAGAGAT	10529
rs145546772	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20984645	AAGTCTTCCCCCATT[C/T]ATTCTCTGTGCACTT	10529
rs145550258	snp	G/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20957146	TCTTTTAATAGCCCA[G/T]AGACACTACTATTCA	10529
rs145564166	snp	A/C			intron-variant, downstream-variant-500B	NEBL	GRCh38.p7	10:20815338	GGCTTTACCACCTTC[A/C]AAGACACGGCTAACA	10529
rs145576533	snp	A/G	0.00597247	0.0543191	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20870932	ACTGGCATAATGTCC[A/G]ATGGCCCATGTTTCA	10529
rs145593777	snp	A/G	0.0119091	0.0762411	intron-variant	NEBL	GRCh38.p7	10:20911090	AATTGCTTGAGCCTG[A/G]GAGGTGGAGGTTGCA	10529
rs145606889	snp	A/T	0.00517822	0.0506191	intron-variant	NEBL	GRCh38.p7	10:20892862	TCTTCACAAGTGAAA[A/T]CATACAAGTTAAATT	10529
rs145610120	snp	A/G	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:21094827	AAAATTAATTTCACC[A/G]AACCAGATTCAGCAA	10529
rs145614525	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20981164	TTCACTGTCTTACAA[C/T]GTAGTACCTGGTCAA	10529
rs145614751	snp	A/C	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21025905	AAATGTCTACCATTA[A/C]TTATAATATTATTAT	10529
rs145625967	snp	A/G	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:21157934	ACACAGGGAGAAGAC[A/G]GCTAGCCATCTATTC	10529
rs145632977	snp	C/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20922666	GATAACTTATAAATA[C/T]AGGCAGAGTCAAGGA	10529
rs145640331	snp	A/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21090519	TCAGGGACTTGATGT[A/T]CTGGAACCTACCCCC	10529
rs145642401	in-del	-/C	0.0298908	0.118541	intron-variant	NEBL	GRCh38.p7	10:20809719	TTAAAATTTACATTA[-/C]ACAGTACAATGAACC	10529
rs145643592	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21090789	GCACCACAGCTCATC[A/G]TTGCTGGCCCCTGCT	10529
rs145649868	snp	C/T	0.0134861	0.0810011	intron-variant	NEBL	GRCh38.p7	10:21024925	GCATCTAACACGAAT[C/T]GGTAGCACCATACAA	10529
rs145654179	snp	C/T	0.0134861	0.0810011	intron-variant	NEBL	GRCh38.p7	10:20997437	CCCCCATCCCTACAG[C/T]CGCAAACCACACCAA	10529
rs145656336	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21063394	AATCACTAATAGTCA[C/T]GAGATGCCTACTATT	10529
rs145671509	snp	A/C	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:20891259	TTCATGAAATCAACA[A/C]GAGAACATATTTATC	10529
rs145673123	snp	C/T	0.140919	0.224948	intron-variant	NEBL	GRCh38.p7	10:20938459	ACCATCATCAAAGAC[C/T]AAAGGTAGATAAAAC	10529
rs145675376	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20925340	GATGGAATATTTGTA[C/T]CAACATTAGGATGGC	10529
rs145676143	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20846315	AAATTCTGCATGAAA[C/T]TGTTATTCAGGCAAA	10529
rs145676258	snp	A/G	0.0138799	0.0821421	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20883203	CATCCACGGACCACA[A/G]CATTTTTCTTTTGAT	10529
rs145681948	snp	G/T	0.00597247	0.0543191	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20784184	TTTTTGCAGTTTTGC[G/T]TTTTCGGTTTTGTCA	10529
rs145700894	snp	A/G	3.30376e-05	0.0040642	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20850370	AATTTACATTAAACA[A/G]TTAGTAACAAACTAA	10529
rs145715141	snp	G/T	0.0252325	0.109451	intron-variant	NEBL	GRCh38.p7	10:20787636	TTTTATTCGACCATG[G/T]GATCCTTTTTGGCAT	10529
rs145724162	in-del	-/TAAGCTC	0.149665	0.228982	intron-variant	NEBL	GRCh38.p7	10:20924478	CTTCGTTCACCAAAA[-/TAAGCTC]TAAGCTCCTCGGAAG	10529
rs145727703	snp	G/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21120617	ATAAAATACCGGTTC[G/T]CTCTCCCATCATCCT	10529
rs145743631	snp	A/G	0.00716266	0.059414	intron-variant	NEBL	GRCh38.p7	10:20794167	GAGGCGAGGGGAAGC[A/G]GACCCCATTTCCTTG	10529
rs145745570	in-del	-/G	0.00557542	0.0525036	intron-variant	NEBL	GRCh38.p7	10:21160653	TAGTGGGGTTGGGGA[-/G]GGTGGGTTGGGGGAG	10529
rs145750576	snp	C/T	0.0279526	0.114869	intron-variant	NEBL	GRCh38.p7	10:21106566	GTTTTGGTACCAGTA[C/T]CAGCCTGTTTTGGTT	10529
rs145756670	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21037622	CTTGATTGTGGCAGT[C/G]GTTACTCAACTATAT	10529
rs145761341	snp	A/T	0.00755907	0.0610114	intron-variant	NEBL	GRCh38.p7	10:20974593	ATTATTTTTCAAAAG[A/T]CTAGATTCTAAACAA	10529
rs145765590	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:20916472	GGTGCAGTGGCACGA[A/T]CTTGGCTCACCACAA	10529
rs145770601	snp	A/G	4.79065e-05	0.00489397	intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20897192	TTTATATCCTCAAAT[A/G]CAGGGACCCTCATTT	10529
rs145770694	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21038048	AGAGAGAGAGAAAAG[A/T]TTGCCTCTAAAGTTA	10529
rs145775005	snp	C/G/T	0.00279242	0.0372774	intron-variant	NEBL	GRCh38.p7	10:21001900	ATATAAGCAAAACTG[C/G/T]TCTCTGTTTTTCCAC	10529
rs145782063	snp	C/T	0.0023933	0.0345097			GRCh38.p7	10:20936950	TTTCATCAAACATCC[C/T]GTTTTTTGCCTGGTA	10529
rs145787811	snp	A/G	0.000399281	0.0141238			GRCh38.p7	10:20977535	GGGAGAGGCATCACA[A/G]ATAGGCGAGCTGGCC	10529
rs145793014	snp	A/G/T	0.00994647	0.0699473	intron-variant	NEBL	GRCh38.p7	10:20969146	GGGAATTAAACAGTC[A/G/T]AAAGGAAAATCTGAT	10529
rs145796830	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20981093	CTGTGCCCAGCCCCA[A/G]CAAATTATTTATTCA	10529
rs145806161	snp	C/T	0.0023933	0.0345097	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20884619	CGATCAGAATAATAA[C/T]ATAACTTACATTATA	10529
rs145813231	in-del	-/A	0.0562307	0.157967	intron-variant	NEBL	GRCh38.p7	10:21168419	GAGATTCTGTAAATC[-/A]GTAGAAATAATAGCA	10529
rs145816965	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20944976	GACCACAGGACTAGA[A/T]TAAGCACTCTCAATA	10529
rs145826219	snp	A/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20890874	AACTATGACTCATTG[A/T]GAAGATGCAGGTAAT	10529
rs145826584	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21015376	CTTTGAGAAGGCTCC[A/G]GAGCCCTGGTTCAGA	10529
rs145830933	snp	A/G	0.00279162	0.0372561	intron-variant, downstream-variant-500B	NEBL, LOC102725112	GRCh38.p7	10:20880507	TTCAGCATCAAGTCA[A/G]GGAAGCTCTGGAAAT	10529
rs145834162	snp	C/T	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21143582	AAAGAAAGGAGAACA[C/T]AGACAAATATCAGAA	10529
rs145846999	snp	C/T	0.00478085	0.0486577	intron-variant	NEBL	GRCh38.p7	10:20798943	TTCATTCCATTTCTA[C/T]TGAGACTAGGAATAC	10529
rs145855470	in-del	-/AACCCCC			intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20899046	ACAACTCTAAGATTA[-/AACCCCC]CAGCCATATCATGCT	10529
rs145858854	snp	A/G	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:20965860	CCTCAGGGCCCTGGC[A/G]TCCCCGAAAGACCCC	10529
rs145863273	in-del	-/GT	0.408017	0.193729	intron-variant	NEBL	GRCh38.p7	10:20799924	CCTACCATCTGGCAC[-/GT]GTGTGTGTGTGTGTG	10529
rs145864502	snp	C/T	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:21042195	GGACTCTGTATTTAA[C/T]GTCTCATTTAATCCT	10529
rs145907604	snp	C/T	0.0123036	0.0774623	intron-variant	NEBL	GRCh38.p7	10:21080328	TTTGATATTGCATTC[C/T]GTGCATGAGACATAT	10529
rs145916622	snp	C/G	0.0103295	0.0711199	intron-variant	NEBL	GRCh38.p7	10:21076349	ACTCAGAAGGCTGAG[C/G]CAGGAGAATCGCTTG	10529
rs145929011	snp	C/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21069718	ACCAGGGTGAGGATA[C/G]AAATCTCATTGCTAA	10529
rs145932528	snp	C/T	0.00597247	0.0543191	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20958786	GTATTTAACAAATCT[C/T]CCATGTTCAATATGT	10529
rs145935415	snp	C/G	0.00438332	0.0466095	intron-variant	NEBL	GRCh38.p7	10:21003261	CTGGGGAACACAGAC[C/G]CACTTGCCTGACCTC	10529
rs145937610	snp	A/G	0.00993419	0.0697739	intron-variant	NEBL	GRCh38.p7	10:20904369	TGGGTACCCTCATTT[A/G]TTAATGAGTTAAAAA	10529
rs145948853	snp	G/T	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20906659	GTGTTGGGGGTGTGG[G/T]TGTGTCTATGTTCAT	10529
rs145968014	snp	C/T	0.0115144	0.0749975	intron-variant	NEBL	GRCh38.p7	10:21116077	TGCATGTCTATTTTA[C/T]ATCTTCCATGACTCT	10529
rs145969390	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NEBL, NEBL-AS1	GRCh38.p7	10:21172308	CAGTGAGTCAGTTCT[A/T]CAAAACAGGCAGGTC	10529
rs145977248	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21066814	ACATCGATTTTCTTA[C/T]ATTGTTCTGCGGTTT	10529
rs145977923	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21076710	ATTCTGATGCATACT[A/G]CAACATGGATGAAAC	10529
rs145984200	snp	C/T	0.0185938	0.0946107	intron-variant	NEBL	GRCh38.p7	10:21000881	AAAAAGGTAGGATGG[C/T]CAGGAAGGGCCACAT	10529
rs145986129	snp	A/T	0.00478085	0.0486577	intron-variant	NEBL	GRCh38.p7	10:21102076	AACTATCCTGAACAA[A/T]TCATTTTACTTCTCT	10529
rs145987579	snp	A/G	0.00953873	0.0683987	intron-variant	NEBL	GRCh38.p7	10:21170022	CAAGTCAAAGTGCAA[A/G]ATAGCTCTTCCCAAC	10529
rs145993524	snp	A/C	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21011269	TTACCCAATAAAATC[A/C]AAGCGTATACAACAG	10529
rs145996137	snp	A/G	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:20920826	ATCAAATGGTACATA[A/G]CTGAAATAAATGGAA	10529
rs146011311	snp	A/G	0.0130921	0.0798413	intron-variant	NEBL	GRCh38.p7	10:20825743	CAATTATCCACAGCA[A/G]ATGTCAAACACTCAA	10529
rs146015390	in-del	-/T	0.00199481	0.0315187	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20873398	AGGGCCAATAATTGC[-/T]TTTACATTATTTTCC	10529
rs146018969	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20917804	TCACTTTCAAGATAC[C/T]TCTTTGAGAAGCCAA	10529
rs146030597	snp	C/T	0.00874735	0.0655527	intron-variant	NEBL	GRCh38.p7	10:20822190	TCTCTGTTTCTCCTA[C/T]AAACCTTGAGGATGC	10529
rs146037349	in-del	-/CTTA/TC			intron-variant	NEBL	GRCh38.p7	10:21066819	ATTTTCTTACATTGT[-/CTTA/TC]TCTGCGGTTTTTCTA	10529
rs146050526	snp	A/G	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:21053119	ATGCCCCATAAATAT[A/G]TACAAATATTATATC	10529
rs146055579	in-del	-/TAAC			intron-variant	NEBL	GRCh38.p7	10:21034328	AATTAACAATAAAAA[-/TAAC]AAGAACAACCACTAC	10529
rs146055855	snp	A/G	0.0244538	0.107838	intron-variant	NEBL	GRCh38.p7	10:20944587	GCTAAAGGCATACAT[A/G]TTTATATGGGTTTGC	10529
rs146060869	snp	A/G	0.00993419	0.0697739	intron-variant	NEBL	GRCh38.p7	10:21016486	TTTTTAAAGAAAGAG[A/G]TAACAGTGGGTAACT	10529
rs146067076	snp	C/T	0.0236746	0.106192	intron-variant	NEBL	GRCh38.p7	10:20948025	TTTTAAGAAAGTTGA[C/T]GGATTTGTGCTGGGC	10529
rs146091016	snp	C/T	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:21155894	CTCTGCAGAGATTAA[C/T]GCCCACTGCATGACA	10529
rs146091668	snp	A/T	0.000798403	0.0199641	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20875332	CTCACTTCATCCCTG[A/T]TGTGTCTTGACTCAA	10529
rs146100004	snp	A/G	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21049257	CCAAGCTGACATATC[A/G]CATTGAACATCACAG	10529
rs146108017	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21082715	AAAGGACTTGAAAAT[A/G]CATTTATTTAAGAAG	10529
rs146119205	snp	C/T	0.0314385	0.121371	intron-variant	NEBL	GRCh38.p7	10:20807967	ATTATTAACAATCAA[C/T]AGTATTTCTCATTTA	10529
rs146122307	snp	C/G	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:20905963	GCAGCACTACCACAG[C/G]TTCTCTATTCCCTTT	10529
rs146131123	in-del	-/AAAA			intron-variant	NEBL	GRCh38.p7	10:21076471	AAAAAAAAAAAAAAA[-/AAAA]GAATTACCACACAAC	10529
rs146136141	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20809162	GAAATCAGGGGTTAG[A/G]GCAAGATCTAAATGA	10529
rs146141362	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20903866	GGCCAATGGAGACTC[A/G]GAAGGGAGAAGGGTA	10529
rs146142401	snp	C/G	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:20843045	CACCAAAACCCGTAT[C/G]TTGAAGCCCTAGCCC	10529
rs146153496	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20847747	CTCTTTCAGTGAAAA[C/T]GTATGTTAACAGCTT	10529
rs146154731	snp	A/G	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:20806876	AGAGACATCAATTCC[A/G]GTATGCTGAACTGAG	10529
rs146177298	snp	A/G	0.00953873	0.0683987	intron-variant	NEBL	GRCh38.p7	10:20996063	TTTAGAGAACAGCGC[A/G]TTCTGGCTCCTAACT	10529
rs146177673	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21035530	AGCTCTTCTTTAAAT[A/G]TACTTATTCCTGGCC	10529
rs146188354	snp	C/T	0.0126979	0.078662	intron-variant	NEBL	GRCh38.p7	10:21000589	GAAGGAGCAAAACAT[C/T]TGTAGAAAAATAAAA	10529
rs146189097	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20936135	TTTCAGTTTATTGCA[C/T]AATAATAACAAAACT	10529
rs146197615	snp	C/G	0.00874735	0.0655527	intron-variant	NEBL	GRCh38.p7	10:20811176	CTGACTTCTGGATTG[C/G]CAAGTAAGTAAATAA	10529
rs146198369	snp	G/T	0.00207506	0.0321438	intron-variant, missense, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20850403	GACCTACTTCACTTT[G/T]CATCTTTTGAGCCTC	10529
rs146211712	snp	C/T	0.00119737	0.0244387	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21138529	TCAATAAAATGTCAT[C/T]GGGAGAGGTGAGGAA	10529
rs146218038	snp	A/G	0.00060942	0.0174453	intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20819425	CAGAAACGACTTGCC[A/G]CACTCAGCTGCTCCT	10529
rs146224621	snp	C/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21101762	CTAAAACAACTTTGT[C/G]CCCAGAGGAAACTCC	10529
rs146226792	snp	C/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21033292	ACATTAGAAGCACAA[C/G]AAGGATCACATTCGA	10529
rs146230816	snp	C/T	0.00517822	0.0506191	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21135334	CTCCCTTAACTCCTT[C/T]GTGTGGTACTTCCCC	10529
rs146241465	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20892308	ATGCTGCACAACCCT[A/G]TGACATTCTGTCTTC	10529
rs146256517	snp	A/C	0.00438332	0.0466095	intron-variant	NEBL	GRCh38.p7	10:20797184	TGAATACTACTGTCC[A/C]TGTTGTATAAATCAA	10529
rs146260489	snp	A/G	0.00914312	0.0669923	intron-variant	NEBL	GRCh38.p7	10:20890103	GTTAAATAAACGGCT[A/G]TCCAGCACAGGATTG	10529
rs146264175	snp	A/G	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20825961	GAAATGGGCAGAAGC[A/G]TGTCTGATAAAAAGC	10529
rs146275785	snp	A/G/T	0.000598727	0.0172927	NEBL	10	allele_origin=G(germline)/T(germline)	10:20828531	TAATGGCTACTCACC[A/G/T]CACTAATGTTTTGTT	10529
rs146275867	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20792987	ATAAGTGGGAGTTAA[A/G]TCCACAAAGTTTATA	10529
rs146293964	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21086303	AGAAATCAATGACAT[A/T]ACAGATTTCTCATTT	10529
rs146296419	snp	A/C	0.0221141	0.102801	intron-variant	NEBL	GRCh38.p7	10:20918591	ACGGCTGGCTCATGC[A/C]TGTAATCCCAGCACT	10529
rs146296811	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21021085	TTATTATATTAGTGC[C/T]CCGTAGCCCAAGTCA	10529
rs146297105	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20975867	GAGATTTAGATAGAG[A/G]TGTTATTTAATCAGT	10529
rs146308690	snp	A/G	0.0178098	0.0926698	intron-variant	NEBL	GRCh38.p7	10:20921260	AATTCACACACACAC[A/G]CACCTACCTGAGTAT	10529
rs146330302	snp	C/T	0.00755907	0.0610114	intron-variant	NEBL	GRCh38.p7	10:21118301	ATCAAAGTGTCACCA[C/T]TTTACAGATATTCTG	10529
rs146340959	snp	A/C	0.00557542	0.0525036	intron-variant	NEBL	GRCh38.p7	10:21082624	AATGGGCTATTTCCT[A/C]ACCTAATTCCGATGC	10529
rs146346114	snp	A/T	0.0162398	0.0886349	intron-variant	NEBL	GRCh38.p7	10:21017394	TTGCTTCTAAAGAAC[A/T]CGACATTTGAGCAAA	10529
rs146349307	snp	A/T	0.00438332	0.0466095	intron-variant	NEBL	GRCh38.p7	10:21115376	CAGATTCAGTTTCCA[A/T]CTGGTATCATTTTCT	10529
rs146353027	snp	C/T	0.000798403	0.0199641	intron-variant, utr-variant-5-prime	NEBL	GRCh38.p7	10:20957900	TTTGACTTCACCATT[C/T]TATTTCACAATTTAT	10529
rs146354268	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20903571	ATCTGCATGTGTTAT[A/G]TTTCTCACAGCACAA	10529
rs146355224	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21001806	ATTTGTTTTGTTTTC[A/T]AATGGAAAATAAGAA	10529
rs146374708	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20842727	AAATATTTACTTTTT[C/T]GTGGCGAGAACATTT	10529
rs146377953	snp	C/T	0.00557542	0.0525036	downstream-variant-500B	NEBL	GRCh38.p7	10:20779853	AGGGAAAAAAGGTAG[C/T]GAATTCTTCAAATAA	10529
rs146384270	snp	A/G	0.00358779	0.0422022	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20877147	AAGGAGGACGAAATA[A/G]AACCAGTAATGTATG	10529
rs146394826	snp	G/T	0.0023933	0.0345097	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20879156	ACTGCATTTAAAACC[G/T]TGACTAATTGACAGT	10529
rs146415247	in-del	-/TT			intron-variant	NEBL	GRCh38.p7	10:20953527	TTTTTTTTTTTTTTT[-/TT]GTAGGCTCTTGGATT	10529
rs146417978	snp	C/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20821521	TAACACCTACAATGT[C/T]ATACTTTTTCATTAA	10529
rs146420935	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20870480	TATATTCATAAGCAG[A/G]ATATCCTCATCAAGA	10529
rs146423130	snp	C/T	0.00676609	0.0577691	intron-variant	NEBL	GRCh38.p7	10:20805131	AGTGAAAGACAAGCG[C/T]CAGGGATGACTCCAA	10529
rs146427052	snp	A/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20960873	TATAAGTGACGCACA[A/T]AATACAGTTCTCGTG	10529
rs146431502	snp	A/T	0.00279162	0.0372561	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20873122	TTCTCAATAAGTATT[A/T]GCTCCAATCTACCAT	10529
rs146434407	snp	A/G	0.00557542	0.0525036	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20872344	GAAAAAAGCTTCCGC[A/G]CCTGATCACTTGTCA	10529
rs146434756	snp	A/G	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:20807064	GGTACAGTGGCTCAC[A/G]CCTCTGATCCCCGCA	10529
rs146440722	snp	C/T	0.00993419	0.0697739	intron-variant	NEBL	GRCh38.p7	10:20902100	CACCATGACCAAGTA[C/T]GCTATTAAGATTTAA	10529
rs146465335	snp	A/T	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:20955855	ATATGGGAAAAAAGG[A/T]TTTCATGAAAAAAGG	10529
rs146469322	snp	A/G	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20998334	TCATGCTAACCTAAG[A/G]AAGGTATGGGGAAGA	10529
rs146471913	snp	A/G/T	0.000610381	0.0174606	intron-variant, synonymous-codon, stop-gained, nc-transcript-variant	NEBL	GRCh38.p7	10:20826479	GATTTTTCTTCACTC[A/G/T]TTCGATCTCTGGGCT	10529
rs146473013	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21059248	TTTTCTGGGTGCCAT[A/T]CCACCAACCCAGGCA	10529
rs146475588	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20992202	ACGTTGGTTTAAAAA[C/T]AGATATTACAGATGT	10529
rs146479748	in-del	-/GA			intron-variant	NEBL	GRCh38.p7	10:20828722	AGGAAAGGAGGAAGG[-/GA]GAGAGAGAGAGTAAA	10529
rs146489574	snp	C/T	0.00914312	0.0669923	intron-variant	NEBL	GRCh38.p7	10:20996480	GGTCTACTGGATCGA[C/T]GCCTTATCACCAACC	10529
rs146489618	snp	A/G	0.00597247	0.0543191	intron-variant	NEBL	GRCh38.p7	10:20953114	CCTGGTATGGACTGA[A/G]CTGTGTACCACCCCA	10529
rs146491098	snp	A/C	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20898782	CCAATTTAATCTAAT[A/C]TACCTACCTACCTAT	10529
rs146511704	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21095010	CCATAGTAGTGTATT[C/T]AAAATCTGACACCAC	10529
rs146513594	snp	C/T	0.00517822	0.0506191	intron-variant	NEBL	GRCh38.p7	10:21162963	AATTTTATTAATTCC[C/T]TACCATGTGCCTGAA	10529
rs146522560	snp	A/C	0.0130921	0.0798413	intron-variant	NEBL	GRCh38.p7	10:21099067	GAGCCCAGGAGCTCA[A/C]GGCTTCAGTGAGCCA	10529
rs146526695	snp	A/G	0.0134861	0.0810011	intron-variant	NEBL	GRCh38.p7	10:21171165	ACATGGAGAAACCCC[A/G]TCTCTACTAAAAATA	10529
rs146554106	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:20914011	CAATAAATTCACCAG[A/T]GCAAACTACACTCAG	10529
rs146554453	snp	G/T	0.00557542	0.0525036	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20857458	TATTCAATAAATTAT[G/T]ATTAATTTTGAGCAA	10529
rs146591266	snp	A/C	0.00597247	0.0543191	intron-variant	NEBL	GRCh38.p7	10:20942286	CAGAAATAATGCCGC[A/C]TATCTACAACCATCT	10529
rs146596138	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20974120	ACCAGCATTGCCATC[C/T]GTGAATAGTAGAGTC	10529
rs146599275	in-del	-/AAA			intron-variant	NEBL	GRCh38.p7	10:20952441	GACTCTGTCTGAAGG[-/AAA]AAAAAAAAAAAAAAA	10529
rs146601168	snp	A/C	0.000153988	0.00877328	missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20812820	TGTGAGGGTGGACCC[A/C]TTTATAGGCAGCATC	10529
rs146607715	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20976522	ATGGAATCAACCCAG[C/G]TGTTCATCAATGGTG	10529
rs146611084	snp	G/T	0.00557542	0.0525036	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20883250	CTGTCAACTGATACC[G/T]TTAAGTCTTATTCAG	10529
rs146625732	snp	A/C	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20804515	AACCAAGCACCGTTC[A/C]ACTTAAGAGAGGGTG	10529
rs146630552	snp	A/G	0.00318978	0.0398085	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21144095	TAATGAGAGGCATCT[A/G]CAGCACTGTTTGTGC	10529
rs146634655	snp	A/G	0.0252424	0.109538	intron-variant	NEBL	GRCh38.p7	10:21076360	TGAGGCAGGAGAATC[A/G]CTTGAACCTGAGAGG	10529
rs146636304	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21064892	GAAAGGAAATTAGGT[A/G]GTTTGGACAAGCAGG	10529
rs146640211	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21078597	ATGACCTGTATACAC[A/G]TATGCAGAGGTATCT	10529
rs146640880	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	C10orf113, NEBL	GRCh38.p7	10:21147880	TCAATTCACTCACAG[A/G]TTCCTTCATGAAACA	10529
rs146659999	snp	A/G	0.00318978	0.0398085	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20898471	CCTTGGCCTTACCTA[A/G]ACTGAAAATCCTGAC	10529
rs146660708	snp	C/T	0.0170251	0.090679	intron-variant	NEBL	GRCh38.p7	10:21168115	ATACATGTTCTCCTT[C/T]GCATGAAATCAAACA	10529
rs146673556	snp	A/G	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:20839316	ATGTGGATTGGACAT[A/G]TCACGGCAACAGAAG	10529
rs146673676	snp	A/T	0.00056076	0.0167352	intron-variant, synonymous-codon, nc-transcript-variant	NEBL	GRCh38.p7	10:20808547	TACCTCACTGCAGCA[A/T]GAAAAGCTAGGGTAA	10529
rs146673922	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20802123	CAAGGCAGGTAAACA[C/T]CAGGTGAGATTGCAA	10529
rs146698857	snp	A/G	0.0138799	0.0821421	intron-variant	NEBL	GRCh38.p7	10:21099916	AACACTTATAACTCA[A/G]TAAGAAACTGTTGAA	10529
rs146708590	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20991411	AGTCACATTTATTAT[C/T]ATAAATTTTGAACAA	10529
rs146708815	snp	C/T	0.0244538	0.107838	intron-variant	NEBL	GRCh38.p7	10:20929878	CCACTGTGCAATATA[C/T]GTATTTAACAAAACT	10529
rs146717111	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21027059	TCTGCTGGAACAAGC[A/G]TCTTGCTTCCTCCTG	10529
rs146722329	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20792237	ATGGGCTTACTTTTT[G/T]AAAAAATCCAGAAAA	10529
rs146727493	snp	C/G	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21030732	GAACAAAGACCACTG[C/G]AAGGAGTCAGATAGG	10529
rs146728104	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20926200	AACTGGTTCCCTTTC[A/G]CCAGGGACAGGATTG	10529
rs146747192	snp	A/C/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20791045	AGAGTTTGAGTTTGA[A/C/T]AGGTTGTTTTATGTC	10529
rs146750078	snp	C/G	0.0023933	0.0345097	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21125536	GCCTCAAAGTAAGAG[C/G]AATGCAAAGGTTGAA	10529
rs146751430	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21170178	TTATTTTTGATCATT[C/T]CTTTTTCTCCCTTAT	10529
rs146755034	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21060083	TAGGGTTTAATGCCC[A/G]GTCATCTAAAAAATA	10529
rs146769214	snp	A/G	0.00835141	0.0640778	intron-variant	NEBL	GRCh38.p7	10:21104010	TTGTTTTCTTTTCAT[A/G]CTTCTGGATATAAAA	10529
rs146781992	snp	A/G	0.00557542	0.0525036	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20882973	TGAGACAGAACTTCC[A/G]ATGTGGGAAGACACC	10529
rs146793598	snp	G/T	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:20886620	ATAGCATAGTGTGTG[G/T]TTAAAAACCTAGACT	10529
rs146796283	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20787033	TCAACAGTTTACCTC[G/T]GTAAGTTTTTTGCTT	10529
rs146796708	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20822623	CTAATATAGACTATA[G/T]AGAGATATACAGACT	10529
rs146812604	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21078043	AATACCAGATTATTC[G/T]GAAAGCTGGGTTGTG	10529
rs146819997	in-del	-/T	0.0748431	0.178382	intron-variant	NEBL	GRCh38.p7	10:21027502	TTTTTGTATTTTTTT[-/T]GTTGAGATGGGGTTT	10529
rs146823462	in-del	-/TCAG	0.437259	0.165632	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21132029	TTTAAAATGTATAAT[-/TCAG]TCAGTTTTAGTATAT	10529
rs146831040	snp	A/G	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:20973063	GCTTCTTAGCTAACC[A/G]TAAGAGCTCCACATT	10529
rs146832532	snp	C/G	0.00795532	0.062565	intron-variant	NEBL	GRCh38.p7	10:21076106	TGTAAAATGGTACAG[C/G]TATTACAAAAAAAAC	10529
rs146838805	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21009893	TTAAGCACACATATA[C/T]GTACTTCATGAGAGT	10529
rs146850533	snp	G/T	0.00676609	0.0577691	intron-variant	NEBL	GRCh38.p7	10:20968823	CCACATTTCTTTAAA[G/T]GGAGATGGTGAGGGT	10529
rs146850708	snp	C/T	0.0267878	0.112589	intron-variant	NEBL	GRCh38.p7	10:21013167	TTAACATCTGCTTAG[C/T]ACGCTGTGCTCCCTG	10529
rs146852977	snp	C/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20911734	TCCTTAGTGTATTCA[C/T]GACTATGTGTTCCAA	10529
rs146861669	in-del	-/ATATAA	0.421842	0.181577	intron-variant	NEBL	GRCh38.p7	10:21061551	ATATATTTTATACAT[-/ATATAA]ATATAAATATAAATA	10529
rs146863169	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21067988	CTCAAAGAAAAAAAA[A/T]TGTAATATACTTCCC	10529
rs146865490	snp	A/G	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:20823772	TAAGGAAATAAATAA[A/G]GAAATAAGGAATTCC	10529
rs146871081	in-del	-/T	0.00914312	0.0669923	intron-variant	NEBL	GRCh38.p7	10:21079285	GTGAAGAGGCAGTAG[-/T]ACCACCATCTTGAGA	10529
rs146871238	snp	A/G	0.0174175	0.0916809	intron-variant	NEBL	GRCh38.p7	10:21109014	TTGCCCGATTGCCCT[A/G]GCCAGAACTTCCAAT	10529
rs146874652	snp	A/G	6.58903e-05	0.00573941	intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20896995	TTTCTGGCCAATTCC[A/G]TGCTTAAGTCTTCAA	10529
rs146898370	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20858571	TTTGTTGTTCACATA[C/T]TCAGGAAGGGTAATG	10529
rs146906814	snp	A/G/T	0.0107391	0.0726353	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20862116	ATGGTTTCTACTAAA[A/G/T]GTGTATCACTTCCAC	10529
rs146930574	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20981772	GCAGCCACCTTGCGA[A/C]CATGAGGTAAGCCTG	10529
rs146938017	snp	C/T	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:20946639	GATAACATTTGTATG[C/T]TTGGTAGAGACGAGG	10529
rs146942028	snp	C/G	0.00517822	0.0506191	intron-variant	NEBL	GRCh38.p7	10:20891659	TAGGCAGACAAATAG[C/G]TCAGTCTTAATTGTA	10529
rs146954588	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21154544	TGGGTCTCAATAACA[C/T]CTGTGTTTAGAAATT	10529
rs146958309	snp	C/T	0.00597247	0.0543191	intron-variant	NEBL	GRCh38.p7	10:20888847	TGAGAACATCAAGTA[C/T]TTATCTGCACGGGAG	10529
rs146970780	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20807779	TGCTGTACTAAAATA[C/T]AACTGCAATGAGGTG	10529
rs146973913	snp	A/G	0.0205511	0.0992634	intron-variant	NEBL	GRCh38.p7	10:21080893	TGGAGTATCACTCTC[A/G]CCCAGGCTGGAGTGT	10529
rs146984044	snp	G/T	0.0103295	0.0711199	intron-variant	NEBL	GRCh38.p7	10:21084482	CCTAGCTACTGGGGA[G/T]GCTGAGGCATGGGAA	10529
rs147000604	snp	C/G	0.00517822	0.0506191	intron-variant	NEBL	GRCh38.p7	10:20903068	TTATAGTAGCCCCCA[C/G]ACCTTATCCATAGAG	10529
rs147004964	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20840980	AATCACACAGCTAAG[C/T]ATTCATGCTTTTTTC	10529
rs147013750	snp	C/T	0.0441095	0.141807	intron-variant	NEBL	GRCh38.p7	10:20805777	AGAACCGTTTGAACC[C/T]GGGAGGCAGAGGTTG	10529
rs147014588	snp	C/T	0.00597247	0.0543191	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20845836	TGCAAATTTAGGAAA[C/T]ATCACTTCTAAAATG	10529
rs147034956	in-del	-/AAAGGAAAAGGGGAAGGG	0.0948562	0.196037	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20882340	GGAGAGGAGAGAGGA[-/AAAGGAAAAGGGGAAGGG]AAAGGGAAAGTAAAA	10529
rs147035842	snp	G/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20931821	CTGGAAGGAGGTAAA[G/T]AAAGTCCCACACTAA	10529
rs147040425	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20997648	ATAATTGGGTACTTT[A/C]TATGATCAGATCTAC	10529
rs147042977	snp	A/C	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20934660	AGAAGGGGCCTGGAT[A/C]CCTGAATGACTGCAT	10529
rs147072939	snp	C/G	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:21032463	TCTATTCATGAATTT[C/G]CTTCCACAGCCATCG	10529
rs147076965	snp	A/G	0.00676609	0.0577691	intron-variant	NEBL	GRCh38.p7	10:20795296	GTGCCAGCCAGGCTT[A/G]TTAGGCTCATAGAGG	10529
rs147079437	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21065932	CAACCTTTCTAGTCT[A/T]ACCACCAGCAGCTGC	10529
rs147081744	snp	A/G	0.00119737	0.0244387	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21133829	AAATCCGAGAACCTT[A/G]AGGAGCTTAGGAACC	10529
rs147086851	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:20927029	AGGCAGTGGTGGTGG[G/T]GGAAAGAAAGGATGG	10529
rs147089790	snp	A/G	0.00953873	0.0683987	intron-variant	NEBL	GRCh38.p7	10:21029327	ATGATGTGACAGAAG[A/G]GTCAATTAAGGAATT	10529
rs147091051	snp	C/T	0.000798403	0.0199641	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21137300	TTGGCATTATAAGAG[C/T]CTGTATATAACAAAT	10529
rs147100940	in-del	-/A	0.120326	0.21374	intron-variant	NEBL	GRCh38.p7	10:20832612	AAGAAAAATGTTATT[-/A]AAAAAAACTATTAAC	10529
rs147103969	in-del	-/T	0.00478085	0.0486577	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20864788	TGCTGCCCAAATTTC[-/T]GTTATAATTGATATA	10529
rs147107642	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20888408	ATTTATCATAGAGAA[C/T]GCTTTCAATGAGACA	10529
rs147109013	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20824287	TTTCAGAAATCACCT[A/G]GTAATGTTTAAAATG	10529
rs147112844	snp	A/G	0.0248432	0.108648	intron-variant	NEBL	GRCh38.p7	10:21168777	ACAGTGGCCGGGCGC[A/G]GTGGCTCATGCCTGT	10529
rs147118746	snp	C/G	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20827653	CACTATTTACAATAG[C/G]AAAGACATGGAATCA	10529
rs147118893	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20791823	AGTACTCAAAAAGAA[A/G]TTCACTGGGGGGGAT	10529
rs147123662	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21171624	GTCCCCTAACTCGTA[A/G]GGTCGTTGTAAAGAT	10529
rs147129041	snp	A/G	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:21164844	TATAACCCAAAAAGA[A/G]AAAAGAAAACTGTCA	10529
rs147138836	snp	C/T	0.00478085	0.0486577	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20881589	AAGTTATCCCCTTGG[C/T]CTCCACTGATACTAT	10529
rs147147865	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:21169050	GAGACTCCGTCTACA[-/A]AAAAAAAAAAAAAAA	10529
rs147151061	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20821411	AGGATCCAGGGTTCA[C/T]GTTCTTTTCCACCAC	10529
rs147151207	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20784998	CAGGGTAAATGCTAC[C/T]AGGGAAATTATATCA	10529
rs147155190	snp	C/T	0.00438332	0.0466095	intron-variant	NEBL	GRCh38.p7	10:20971044	ACGGATCCTGTAGTG[C/T]CACAAAAGAGACAAA	10529
rs147155389	snp	A/T	0.00597247	0.0543191	intron-variant	NEBL	GRCh38.p7	10:20912930	CTCTGTTACCCAGGC[A/T]TTAAGGTTTTTGGTA	10529
rs147160117	in-del	-/GTTGTTGTT	0.0898077	0.191933	intron-variant	NEBL	GRCh38.p7	10:21122003	TGGGGATTTCTCCTG[-/GTTGTTGTT]GTTGTTGTTGTTGTT	10529
rs147169890	in-del	-/GA			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21138001	AACTGGAAGTGGATG[-/GA]GAGGAGCCCAGCATG	10529
rs147171574	snp	A/G	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:21161559	CAATAGGACAGACTC[A/G]TGTATCAATAAAAAC	10529
rs147188012	snp	A/G	0.00597247	0.0543191	intron-variant	NEBL	GRCh38.p7	10:21007738	CACAGAGAAAGACCC[A/G]CTAAAACAGGTAAAG	10529
rs147198252	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20910971	CTAGGAGTTCAAGAA[C/T]AGCCTGGGCAACACA	10529
rs147216835	in-del	-/AAC	0.00438332	0.0466095	intron-variant	NEBL	GRCh38.p7	10:20946005	AAAAATAAGTGAAAT[-/AAC]AAACATGAAAGATGG	10529
rs147218210	snp	A/G	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21107957	TAGTTTATTTGCATA[A/G]AGTTATTTATGGTAT	10529
rs147223120	snp	A/G	1.65091e-05	0.00287303	missense, intron-variant, utr-variant-3-prime	C10orf113, NEBL	GRCh38.p7	10:21126028	CTCCGCAGCCACCTG[A/G]CAAGCGTTGGCCAGC	10529
rs147228225	snp	G/T	0.0741063	0.177655	intron-variant	NEBL	GRCh38.p7	10:21109943	ATGTTGTTAGTCTTT[G/T]CAAAAAACCAGCTCC	10529
rs147231203	snp	A/G	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:21003783	AATTCTGCTTTTCAT[A/G]GGAACTAGCCTTTGC	10529
rs147244633	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20869127	ATTCTCAGGAACTGT[C/T]CTGGCCATACTTGAT	10529
rs147257623	snp	A/G	0.00438332	0.0466095	intron-variant	NEBL	GRCh38.p7	10:20806182	GGTTTTTACAGCCTT[A/G]GAGGAGAGAATGCAA	10529
rs147259591	snp	A/G	0.00557542	0.0525036	intron-variant	NEBL	GRCh38.p7	10:20954725	CCCCACCACCACCCC[A/G]CCCCCTCTGCAAACA	10529
rs147260982	snp	C/T	0.0221141	0.102801	intron-variant	NEBL	GRCh38.p7	10:20900557	GGCTGGGTGCGGTGG[C/T]TCACGCCTGTAATCC	10529
rs147261018	snp	A/T	0.00398564	0.0444627	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20864946	CGATAGCTATAATGT[A/T]AGTTAAAAATTAAAA	10529
rs147263249	in-del	-/G	0.121369	0.214369	intron-variant	NEBL	GRCh38.p7	10:21117882	TATGACCTTACATAA[-/G]GTTATCTAACCTGAG	10529
rs147274457	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20803206	ATACCACTGTAGGAT[G/T]ACTATAGTTAGCAAG	10529
rs147276749	snp	A/G	0.00398564	0.0444627	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21143224	GAGGCCAAGGTGGGC[A/G]GATCACTTGAAGTCA	10529
rs147278809	in-del	-/CACA			intron-variant	NEBL	GRCh38.p7	10:20947682	TTTTTACTGAGAAAT[-/CACA]CACACACACACACAC	10529
rs147295044	snp	C/T	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:20990308	TATGTTTGTGTCCTC[C/T]CCAAATTCATATGTT	10529
rs147303096	snp	A/G	0.00835141	0.0640778	intron-variant	NEBL	GRCh38.p7	10:20951437	ACATAATCCTTCCAG[A/G]AAAATGCAAAGTAAA	10529
rs147304546	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20896057	CCAGGACTGACTTCC[A/G]TTAGAAAACAAACGT	10529
rs147305131	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20993587	TAGACGGCAGCTATA[A/C]AGAACATGTTCTCAC	10529
rs147322727	snp	A/C	0.0182019	0.0936463	intron-variant	NEBL	GRCh38.p7	10:21093346	GTTGGACAAAATTTT[A/C]TAGGTGAGAAAAAAA	10529
rs147329912	snp	A/G	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:21164263	GAACTGAAACAGAAC[A/G]GAAACGTAATTGATT	10529
rs147332648	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21053799	GCACTTTGGGAGGCC[A/G]AGGCAGGTGGATCAC	10529
rs147333064	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21097797	CATTCCCCTGAAACA[C/G]GACAGGAACCGCCCA	10529
rs147362530	in-del	-/G	0.181659	0.240478	intron-variant	NEBL	GRCh38.p7	10:21051701	ATTAAATTCCCCAGT[-/G]AAAAGACACAGATTG	10529
rs147363334	snp	A/T	0.00874735	0.0655527	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20855883	ATAATTTTGGCAGAA[A/T]ATCTCTTATTGAGCA	10529
rs147365241	snp	G/T	0.0232847	0.105357	intron-variant	NEBL	GRCh38.p7	10:20792019	AAAAAAATTATTTGT[G/T]CAGTGAAGCCACAGT	10529
rs147369670	snp	C/T			intron-variant, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20884747	ACTCTCATTAAGCTG[C/T]AGTTCCAATGCCTGA	10529
rs147379763	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20852427	TTAATATTCTCAGGA[C/T]TTATTCTTTTCTGCA	10529
rs147396244	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21039365	TGGTTTTGGGTTTTA[C/T]GTTTAAGTCTTTAAT	10529
rs147399252	in-del	-/GT			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21142999	TTAAGTGTGTGTGGG[-/GT]GTGTGTGTGTGTGGG	10529
rs147408240	snp	C/T	0.0689305	0.172377	intron-variant	NEBL	GRCh38.p7	10:20937874	GATCAAACTGCAAGG[C/T]GGCAGCAAGGGTGGA	10529
rs147413104	snp	A/G	0.00676609	0.0577691	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20882086	GGGAGGCTGAGGCAG[A/G]AGGATTGCCTGATCC	10529
rs147430928	snp	A/G	0.00398564	0.0444627	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21142699	GGCAGACGGTATGGC[A/G]AGCATTACTGCTACT	10529
rs147430943	snp	C/G	3.29544e-05	0.00405908	intron-variant, missense, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20880844	TAACCTCAGGGGGCT[C/G]CTTCATGTGGGCATA	10529
rs147438706	snp	A/G	0.00438332	0.0466095	intron-variant	NEBL	GRCh38.p7	10:21036179	AAAAAAGAAAGAAAA[A/G]GACAGGCACAGTGGC	10529
rs147439249	snp	A/G	0.0763149	0.179815	intron-variant	NEBL	GRCh38.p7	10:21077254	CAAAGGAATTGGGGG[A/G]AGAAAAGCTTTGTTC	10529
rs147440467	snp	A/G	0.000798403	0.0199641	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21145726	AGAATCAGATCTACC[A/G]GTCAGTACTCTTTGG	10529
rs147468667	snp	A/G	0.0119091	0.0762411	intron-variant	NEBL	GRCh38.p7	10:20837981	TAATGTTCAGTTACA[A/G]TGCACCTGGTCACCA	10529
rs147473463	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20927128	GGAGGATAACTAAGT[C/T]TCTACTCTGGCCACT	10529
rs147473966	snp	C/T	0.00557542	0.0525036	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20872559	GAACCACAGCAACTC[C/T]ATCTTGAGAAGGGAA	10529
rs147498277	in-del	-/C	0.0298908	0.118541	intron-variant	NEBL	GRCh38.p7	10:20806093	GGCTTAGGATAGGGT[-/C]CTCTTGCTAGAAATA	10529
rs147500979	snp	C/T	0.00835141	0.0640778	intron-variant	NEBL	GRCh38.p7	10:21025579	AAATGCAGGAAGCGA[C/T]ATAAGCAAATGGCAA	10529
rs147506484	in-del	-/C	0.0569829	0.158885	intron-variant, upstream-variant-2KB	NEBL, NEBL-AS1	GRCh38.p7	10:21173472	GGTGCCCAGCCTGGT[-/C]CCCTCCGGGGTCCGG	10529
rs147507087	in-del	-/T	0.00438682	0.0466279	intron-variant	NEBL	GRCh38.p7	10:20803549	AGAAGAAAAATAGCG[-/T]TTCTAAATATTTATA	10529
rs147516110	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20925114	GACCCAGATCCCCCA[G/T]GCTCCTTTTGTAGAG	10529
rs147516483	snp	A/T	0.00358779	0.0422022	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20958281	ATGTGATGTACAAAG[A/T]TATTTCTGCCATTTC	10529
rs147517166	snp	C/T	3.32436e-05	0.00407685	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20869713	GTAAGAAATCATTTC[C/T]GTTCAAGGTTTAGAA	10529
rs147530694	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20789027	ACTGTCCACTATGTT[C/T]AAGGCATGCCAGGAA	10529
rs147534757	snp	A/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21123448	TATCATCAACTTTAT[A/T]CATACACTGAAGATA	10529
rs147535381	in-del	-/T	0.0146672	0.084371	intron-variant	NEBL	GRCh38.p7	10:20817912	GTCTTCAATAAATGC[-/T]TTCCTCTTCAATATC	10529
rs147544047	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21021410	CTGGCCTCCTGTCTG[C/G]CAAGGCCCCCATGGC	10529
rs147551221	snp	C/T	0.00676609	0.0577691	intron-variant	NEBL	GRCh38.p7	10:21119140	TATTTTTGTGGATAC[C/T]ATGTCTTCTAGCTTT	10529
rs147554168	snp	C/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21014835	TGTTCCCTATAAAAA[C/G]AAATCACTTTTACTT	10529
rs147564343	snp	A/G	0.00438332	0.0466095	intron-variant	NEBL	GRCh38.p7	10:21018806	AGGCCGAGGCAGGTG[A/G]ATCACAAAGTCAGGA	10529
rs147564884	snp	A/G	0.0111196	0.0737302	intron-variant	NEBL	GRCh38.p7	10:20949166	GATTGCCCTGGCCAG[A/G]ACTTCCATTCTCAGC	10529
rs147581181	snp	A/C	0.00597247	0.0543191	intron-variant	NEBL	GRCh38.p7	10:20814293	TGACCAATAGTAACT[A/C]TCTATCTAGTCTGTA	10529
rs147584483	snp	A/T	0.0310518	0.120672	intron-variant	NEBL	GRCh38.p7	10:21157431	AAAAATTAGCTGGGT[A/T]TGGTGGCACGTGCCT	10529
rs147594105	snp	A/C	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21115776	TATTTTTCAGCCACT[A/C]TTTCTTTAGATTTTT	10529
rs147597660	snp	G/T	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:21051256	TATTGTAATTCTCAT[G/T]TGTAATCCATGCTTT	10529
rs147610771	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20907552	TTACCTCAGATAACC[A/G]AATTTAAGCAAACCA	10529
rs147614398	snp	A/G	0.0103295	0.0711199	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20849696	CCAGAACTGAAAGAA[A/G]TTAATCTCTGTTCTT	10529
rs147622517	snp	C/G	0.00259108	0.0359002	intron-variant, stop-gained, nc-transcript-variant	NEBL	GRCh38.p7	10:20888199	TTTAATGGTGCCTTT[C/G]TATTTTGCCTGGGGG	10529
rs147624038	snp	A/G	0.00557542	0.0525036	intron-variant	NEBL	GRCh38.p7	10:20810697	GCATCAGATCCTAAA[A/G]TAAGCTGTTTACAGC	10529
rs147627047	snp	C/T	0.0107246	0.0724382	intron-variant	NEBL	GRCh38.p7	10:21154955	CCTGTAATCCCAGCA[C/T]TTTGGGAGGCCGAGG	10529
rs147652933	snp	C/T	0.0193772	0.0965046	intron-variant	NEBL	GRCh38.p7	10:20905137	CATATTGCAAACAAC[C/T]ATTAGAACTATAACT	10529
rs147653406	snp	C/G	0.00597247	0.0543191	intron-variant	NEBL	GRCh38.p7	10:20938194	AGGCACCCCCCAGTA[C/G]GGGCAGACTGACACC	10529
rs147655230	snp	A/C	0.0107246	0.0724382	intron-variant	NEBL	GRCh38.p7	10:21105685	AGCATGATTTATAAT[A/C]CTTTGGGTATATACC	10529
rs147659824	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21036817	GAGGCCAGAGATGAG[C/G]AATATTAGGCCTGGA	10529
rs147660271	snp	C/T	0.00557542	0.0525036	intron-variant	NEBL	GRCh38.p7	10:20997765	AGCAATAACTGAAAA[C/T]ATTAGATGCTTGAGA	10529
rs147669416	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20936732	TTTAGGATTACCACT[A/C]ATTATAGTTTAATTT	10529
rs147669794	snp	A/G	0.0322114	0.122752	intron-variant	NEBL	GRCh38.p7	10:21001753	TGATTGCAAAAATTC[A/G]AAAACCTGCAACCTC	10529
rs147685791	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20801759	CCCTCTTGATATATG[C/T]TATGAACAATAAACT	10529
rs147688228	snp	C/T	0.0111196	0.0737302	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21140036	CGTGGTTTCAGGTGC[C/T]TGTAATCCCAGCTAC	10529
rs147697345	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21103982	GCTGTGAGGTAAGTG[A/C]TCAGGTTTTGTTTTG	10529
rs147702792	snp	C/T	0.00676609	0.0577691	intron-variant	NEBL	GRCh38.p7	10:21034383	CTAGCTTATGGGCTA[C/T]CTCCTGTGCTCAGAG	10529
rs147713650	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20948599	AATGAGGGGAATAAA[C/T]GGTTAACTGCCAACA	10529
rs147717325	snp	A/G	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20892904	GGAAGGAAAAACAAT[A/G]GCTCCATCATTATTT	10529
rs147726802	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20862032	TTTACACACGTTGAA[C/T]ATCTCATATAATTTG	10529
rs147727818	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20798572	AATGTTCAACCATCC[A/G]ATAAGCAGGAATATT	10529
rs147730469	snp	A/G	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21137509	GTTTGCTCCTGCTCC[A/G]TGTCTAAGAACACTA	10529
rs147733065	in-del	-/CCATC	0.0452528	0.143452	intron-variant	NEBL	GRCh38.p7	10:20922762	TTCTGAGCACTCGAG[-/CCATC]CCATCCCTTCCGTTG	10529
rs147745538	in-del	-/C	0.0236746	0.106192	intron-variant	NEBL	GRCh38.p7	10:21161033	ATTGCATGTCAGTGA[-/C]CCGTAATCCAGCTGC	10529
rs147758423	snp	A/G	0.0115144	0.0749975	intron-variant	NEBL	GRCh38.p7	10:21088597	CCAGGTACTTCCTGC[A/G]GGGATGGAAACTAGA	10529
rs147764807	snp	C/T	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20977684	TGGGGTGAAAAAAAA[C/T]TGTGAAATCAGTGGT	10529
rs147764902	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21021914	GAGGGAGCAGAACAA[C/T]CACACAAGGAGCCCA	10529
rs147774417	snp	C/T	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20981166	CACTGTCTTACAACG[C/T]AGTACCTGGTCAAAC	10529
rs147791122	snp	A/C	2.07587e-05	0.00322164	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20785722	GGATACATTAGAATA[A/C]AGCTCAAAGGGCAGG	10529
rs147791301	snp	A/G	0.0221141	0.102801	intron-variant	NEBL	GRCh38.p7	10:21119284	TTTTGAAAAATTTCA[A/G]ACCTGCAGAACAGCT	10529
rs147801352	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21084246	GTGTGGTTTATGCGT[C/T]GAGTGTTGAATGCAG	10529
rs147802640	snp	A/C	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:21124468	TGCTTACAGAGTGGC[A/C]GTTTCTCCCTGAGCT	10529
rs147820681	snp	G/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20936555	TCCTTTTACAATTAG[G/T]TCTGGCCTTAGAGCA	10529
rs147820888	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20840141	CAGAGTTTCAAAATA[C/T]GGGGACAAGGCTTTA	10529
rs147822117	snp	C/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20880158	ACAAAGTCAGGAGCT[C/G]AAGACCAGCCTGGCC	10529
rs147833312	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20781000	AATGCTGTTGTACAT[G/T]ATGCAGGGGAAATAA	10529
rs147834097	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21116389	CTCTCTCTTCTTCTT[C/G]TTATAAAGTTATTAA	10529
rs147837364	snp	A/T	0.000798403	0.0199641	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20878248	GAGAGACATCTTGGT[A/T]CACTAAAAGATATTA	10529
rs147847870	snp	C/T	0.00438332	0.0466095	intron-variant	NEBL	GRCh38.p7	10:21033708	TTGCACCACTGCACT[C/T]CAGCCTGGCAACAAG	10529
rs147853461	in-del	-/TCTC	0.00478085	0.0486577	intron-variant	NEBL	GRCh38.p7	10:20988601	TCCATCATCAAATTG[-/TCTC]TCTCTATTGGGTCAC	10529
rs147853594	snp	C/T	3.3018e-05	0.00406299	intron-variant, missense, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20858271	CTGGCTTTCAAAACA[C/T]GGTCTAAAAACAACA	10529
rs147860335	snp	A/C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20968233	ATTAGGGCCAGGCAC[A/C/T]GTGGCTCCTGCCTGC	10529
rs147863071	snp	A/G	0.0158469	0.0875917	intron-variant	NEBL	GRCh38.p7	10:20934504	CTGTGGAATATGGAT[A/G]GACGTGACGTGCATG	10529
rs147865027	snp	A/C	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21032358	ATCAGCCAAAGGCAT[A/C]ATTATAATGACTATA	10529
rs147869691	snp	C/T	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20960926	GTTTGCTCATACTTT[C/T]ATGTCACTCACACAT	10529
rs147876978	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20965152	AGCACCTACTATGGG[C/T]CAAGAGCTGTTCCAG	10529
rs147889547	in-del	-/TT	0.104859	0.203554	intron-variant	NEBL	GRCh38.p7	10:21049101	TAAAGCCCTCAACTC[-/TT]TAAATGAGACTTACC	10529
rs147899744	snp	A/G	0.00835141	0.0640778	upstream-variant-2KB	NEBL	GRCh38.p7	10:21175756	AGCTGTCTTTTAAAA[A/G]TATTTCAGAGCTCAT	10529
rs147901148	snp	C/T	0.000116359	0.00762667	intron-variant, missense, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20859771	GCACTTTCAAGAGGA[C/T]TGTAATGATGTTTCT	10529
rs147926272	snp	A/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20922210	ATCAGCCAGGCTGTG[A/T]CTCTGGCTGAGAATT	10529
rs147927388	snp	A/G	0.00795532	0.062565	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20866223	TTCTGGGAAGGGGGC[A/G]TTGGGGAGTTATTAT	10529
rs147943936	snp	C/T	0.0154538	0.0865337	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20862131	TGTGTATCACTTCCA[C/T]GCCATGGTAAGGTTA	10529
rs147946782	in-del	-/AGTGC	0.0209421	0.100162	intron-variant	NEBL	GRCh38.p7	10:21125011	ATCAGTCTCCACTGA[-/AGTGC]AGTGTTGAGAGGTGA	10529
rs147963505	in-del	-/TTTG	0.0368353	0.130617	intron-variant	NEBL	GRCh38.p7	10:21102814	TTTGCACACATGTTT[-/TTTG]TTTGTTTGTTTTATT	10529
rs147969608	snp	A/T	0.0134861	0.0810011	intron-variant	NEBL	GRCh38.p7	10:20952020	CATGTGAAGTCCACA[A/T]TCTGAACTACATAAT	10529
rs147969789	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20919162	TGTGGCAAGAGAAGG[C/T]ATCTGAGCTATAGTT	10529
rs147970541	snp	C/T	0.00636936	0.0560724	intron-variant	NEBL	GRCh38.p7	10:21038611	TTATCCAGTCTATCA[C/T]TGATGGGCATTTGGG	10529
rs147973263	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20970240	ACTCCTTACTGTACA[C/T]ACATGTTGACTCACT	10529
rs147974969	snp	A/C	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20891814	GTTAGAAGTCACACA[A/C]AATCATGTGTGATTT	10529
rs147978374	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20827915	CAACACACACAGGGG[C/T]CTATCAGAGGGTGAA	10529
rs147982517	snp	C/T	0.00676609	0.0577691	intron-variant	NEBL	GRCh38.p7	10:20937474	TGGAGACAAGATGGT[C/T]GAATAGGAACAGCTC	10529
rs147983108	snp	A/G	0.0130921	0.0798413	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20881455	CCATCCATTACCACC[A/G]TGTTGAATTTCCTCC	10529
rs147988015	snp	C/T	0.0275645	0.114116	intron-variant	NEBL	GRCh38.p7	10:20796228	ATTAGCAGGGCGTAG[C/T]GGTGGGCGCCCGTTA	10529
rs147992558	snp	A/G	0.00874735	0.0655527	intron-variant	NEBL	GRCh38.p7	10:21066630	TTATTTTAAGCCTCC[A/G]AATTTGCTTTAAAAA	10529
rs147993968	snp	A/G	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21134002	GAGGCTGAGGTAGGC[A/G]GATCACTGGATGTCA	10529
rs148010303	snp	A/C	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:21171846	TCTACTACAAACGAC[A/C]TACTACTAACCAGCC	10529
rs148013446	snp	A/G	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21076577	CATGGTCATAGCAGC[A/G]TTGACCACAACAGAT	10529
rs148027536	snp	A/G	0.00438332	0.0466095	intron-variant	NEBL	GRCh38.p7	10:20917284	CTAACAATCACTAAT[A/G]TTGTATTTTCACATT	10529
rs148029865	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20833350	AATAAGATCCATTGA[A/C]TTTATTTGAAAAATA	10529
rs148065204	snp	C/T	0.0115144	0.0749975	intron-variant	NEBL	GRCh38.p7	10:21015844	AGGGGTCTTTCATCT[C/T]GCCTGGATGTTTTAA	10529
rs148070879	snp	A/C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20926602	TTACTATAGGACTTA[A/C/T]GCTCCAGGAAAGAAA	10529
rs148072440	snp	A/G	0.00199481	0.0315187	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20871957	GGCTCTCAGGTGAAA[A/G]CAAACCCAAATTATC	10529
rs148079637	snp	C/T	8.24219e-05	0.00641905	intron-variant, missense, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20868678	CTTGACTAGAAAGTT[C/T]AGAAGCTTCCACGGC	10529
rs148104273	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21120831	ACACAACTCTGCGTC[A/G]GCTGCTATGAAGATA	10529
rs148107151	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21056596	AATCCACTCCTAGGT[A/G]TATCTTCTAGAGTTG	10529
rs148117675	snp	C/T	0.0107246	0.0724382	intron-variant	NEBL	GRCh38.p7	10:21021099	CCCCGTAGCCCAAGT[C/T]AGAAAGCTGGGAGTA	10529
rs148126554	snp	C/T	0.00557542	0.0525036	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20876194	AAAGTTTTCAGTCTT[C/T]CAAAAGAAGGAGTAA	10529
rs148130222	snp	C/T	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:21068957	CAAGTGGCAAGATCA[C/T]GGCTCACTGCAGACT	10529
rs148141774	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20963457	AGAGAAGGCACAATC[A/C]CATATTATTTTTGTT	10529
rs148143056	snp	G/T	0.00517822	0.0506191	intron-variant	NEBL	GRCh38.p7	10:20905747	TTGAAAGAACCAAAA[G/T]TTCTATGTCACTGGA	10529
rs148147399	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20820431	TCTCATTAGAAGAAA[C/T]TTCACAGGGACAGTT	10529
rs148147449	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21163933	TAAATAAAATTAATA[C/T]GGGATTTCCAGTGAT	10529
rs148175522	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21045685	ATCGCCTCACACTTG[G/T]TAGGATGGATGTTAT	10529
rs148179937	snp	C/G	3.30235e-05	0.00406333	intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20814010	TCAGACTTGGTCTAC[C/G]TTTCATCTGTTTATG	10529
rs148181577	snp	A/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21006659	CTTTTCCAAAGGAGG[A/T]GTTGCATGGCTTTCA	10529
rs148189033	snp	C/T	0.0111196	0.0737302	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20862673	CCATGGAACAAGGCA[C/T]AACCCTTTCAGTTTT	10529
rs148198345	snp	A/T	0.00398564	0.0444627	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20852164	CACTTATAATTGAAA[A/T]AAGAAATTATAATAA	10529
rs148206494	snp	A/G	0.0126979	0.078662	intron-variant	NEBL	GRCh38.p7	10:21101110	ATGGGGTAGAAAGGT[A/G]AGCCTGTCTCCTAGC	10529
rs148224900	snp	C/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21042757	GACCAGCAAACCTCT[C/G]GATTCTTCCTGCAGA	10529
rs148237609	snp	A/G	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:20943758	ACGTAAAACTAAGTC[A/G]TTCAAAACTATTCAG	10529
rs148238258	in-del	-/A	0.0479149	0.147179	intron-variant	NEBL	GRCh38.p7	10:21064908	GTTTGGACAAGCAGG[-/A]AAAAAAAAATATTTA	10529
rs148244898	snp	C/T	0.00478085	0.0486577	intron-variant	NEBL	GRCh38.p7	10:20802762	ACTCGAAAGAAGGAA[C/T]GAAAACTGTGACTCT	10529
rs148263288	snp	A/T	0.0267878	0.112589	intron-variant	NEBL	GRCh38.p7	10:21155309	TTCTATTAGTTATTT[A/T]TAAATGTACAATTAA	10529
rs148267116	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21085859	CATTTACATCTCACT[C/T]GGCAGGGCAGGCAAG	10529
rs148278297	in-del	-/AA	0.235854	0.249599	intron-variant	NEBL	GRCh38.p7	10:20977265	TACTGACCTAAAGTT[-/AA]AAGAGAAAGAAAGTG	10529
rs148281822	snp	A/G	0.00795532	0.062565	intron-variant	NEBL	GRCh38.p7	10:20978292	CTAATCAGAACACCA[A/G]ATCTTTTTAGTTTTC	10529
rs148285275	snp	C/T	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20899069	ATCATGCTGGCCCAG[C/T]GTAGTGGATTCCACA	10529
rs148296540	snp	C/T	0.0166325	0.0896639	intron-variant	NEBL	GRCh38.p7	10:20806264	CCAAGCAGAGGCCCT[C/T]CGAATTCCTGATCTC	10529
rs148308393	in-del	-/CT	0.0659589	0.169201	intron-variant	NEBL	GRCh38.p7	10:20814763	AATGCATACAAGCTA[-/CT]CTCTATTTCTTTTTA	10529
rs148321393	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21091065	AGGTCAACTCCACCT[C/T]CTGAACCTCTCTCGG	10529
rs148323668	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21025506	CTCTGTGAGATTCAG[C/T]TGTTAAAAATATAGG	10529
rs148338645	snp	G/T	0.0349115	0.127424	intron-variant	NEBL	GRCh38.p7	10:21034651	TAAAGAACTGTCCTT[G/T]GGGAGAGGAGGAAAC	10529
rs148351497	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20935271	ACAAAGATCACAACA[C/T]AGATTCATTTCTGGA	10529
rs148358227	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20791735	TCTGAAACTGGAAAA[C/G]AGGAAATATACGTAA	10529
rs148362515	snp	C/T	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21126701	CCACTGGGCCAGGTG[C/T]GGTGGCTCATGCCTG	10529
rs148368042	in-del	-/TCCCTACCTC	0.0123036	0.0774623	intron-variant	NEBL	GRCh38.p7	10:21121348	TCTTCCAAGGTTCAG[-/TCCCTACCTC]TCCCTACCTCTTGAG	10529
rs148417425	snp	A/G	0.031825	0.122064	intron-variant	NEBL	GRCh38.p7	10:20789911	TGTATAGATATATGT[A/G]TATATATATGTGTGT	10529
rs148420869	snp	A/G	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21058025	GATACATCACTTTGA[A/G]AACAGGGCAAATTTC	10529
rs148422335	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21124494	GAGCTGTCTAAAGAC[C/T]CTAATGCAATGAAAC	10529
rs148422933	in-del	-/GTT/GTTGTT/GTTGTTGTT			intron-variant	NEBL	GRCh38.p7	10:21122002	GTTGTTGTTGTTGTT[-/GTT/GTTGTT/GTTGTTGTT]TTGAGACACAGTCTC	10529
rs148427760	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20907265	GTCTTCAGTGTGGAA[A/T]TGTATTTTATTAAGG	10529
rs148428319	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20964833	GACATCACCATCTGA[C/G]CACCTGAATTTAACT	10529
rs148438237	snp	A/T	0.0146672	0.084371	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20877485	AAAGCAGCCCCGAAG[A/T]CTTTTTCTTTTCTAA	10529
rs148441223	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20810255	AATCCCCAGTCACTC[C/T]TGCTCTCCACAGGCT	10529
rs148444501	snp	C/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21003650	TTCTTGAATCGACTT[C/T]GGTTGTACACATCCT	10529
rs148458122	snp	C/T	0.02016	0.0983543	intron-variant, downstream-variant-500B	NEBL, LOC102725112	GRCh38.p7	10:20884961	CTCTCTCTCTTTTTC[C/T]GGCATTTCTTCCTTT	10529
rs148460235	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20821535	TTATACTTTTTCATT[A/G]AATTAATTCACTGTT	10529
rs148465314	snp	A/T	0.00795532	0.062565	intron-variant	NEBL	GRCh38.p7	10:21165940	CTAGTGTTTCTCATA[A/T]CTTTCAATCACCACT	10529
rs148465848	snp	C/T	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:21070431	CTCAATAATATATCA[C/T]GTATGTATTTTTTCA	10529
rs148481274	snp	A/G	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:20911341	ATCTTCTATGTTGAT[A/G]TATACACCTGTTGTG	10529
rs148482502	snp	A/G	0.030278	0.119257	intron-variant	NEBL	GRCh38.p7	10:21107696	ATAAAATGAGTTAGG[A/G]AGGATTCCCTCTTTT	10529
rs148483451	in-del	-/ACTC			intron-variant	NEBL	GRCh38.p7	10:20806004	ACCCATCCATGTGTT[-/ACTC]ACTCAAATTCTAGTA	10529
rs148498924	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20921421	AATGGAGGCAGGAAC[A/G]GGAGATCAGATGACA	10529
rs148502279	snp	C/T	0.00279162	0.0372561	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20864399	GAAAGTTTACAACTA[C/T]GGGAGCAAAGCTATT	10529
rs148506474	in-del	-/GCATAGTCTATGCGT	0.0197687	0.0974348	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20961539	TACCAGATGAAATTG[-/GCATAGTCTATGCGT]GCACTGAGTACTGCT	10529
rs148511822	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21170197	TTTCTCCCTTATCCA[A/G]TTCTCTCTCATTGTT	10529
rs148526359	snp	A/C	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21151853	AAACTTATCTCTTCC[A/C]CTGCTCCATTTTTCT	10529
rs148537202	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21110503	TGTCATTTCTGTCAT[C/T]CCTGGTATTGGTTCT	10529
rs148539432	snp	A/G	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21045932	CGCATGTTTATCACA[A/G]CACTATTCACAATAG	10529
rs148541027	snp	C/T	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20951018	CTCATACCTGTAATC[C/T]CAGCACTTTAGGAAG	10529
rs148551893	snp	A/G	9.96843e-05	0.00705919	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20869714	TAAGAAATCATTTCC[A/G]TTCAAGGTTTAGAAA	10529
rs148555761	snp	A/C	0.00835141	0.0640778	intron-variant	NEBL	GRCh38.p7	10:20803997	TACTTATATATATTT[A/C]TGCATGTGGTCCTTG	10529
rs148557663	in-del	-/T	0.0807149	0.183963	intron-variant	NEBL	GRCh38.p7	10:20982219	TTACAGAAAATTCGG[-/T]AAACATCGTCAAATG	10529
rs148573370	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20812389	AGGTTTGTTACATAC[A/G]TATACATGTGCCACG	10529
rs148577673	snp	C/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21088304	CCAGGAGGTGGTGAT[C/G]AGTCTGGGCAACATA	10529
rs148578613	snp	A/G	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:21156873	AAGGTCACAATCATG[A/G]GTTTTTCCCCCTTCT	10529
rs148581852	snp	G/T	0.0217236	0.101931	intron-variant	NEBL	GRCh38.p7	10:21061517	TATTACATTATATAT[G/T]ATATATCACATATTA	10529
rs148584471	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20994592	GGCATTGACCCCCCC[A/G]TACACTCAAAAATCT	10529
rs148587116	snp	A/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21050356	TTAAACACATTAAAA[A/T]CAATTCTCACAGCCA	10529
rs148588810	in-del	-/C	0.354665	0.227036	intron-variant	NEBL	GRCh38.p7	10:20981414	ATCTCATAAAAAAAA[-/C]ACACACAAAATTATA	10529
rs148594079	snp	A/G	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20900693	AAAAAAATTAGCCGA[A/G]TGTGATGGCAGTAGA	10529
rs148601756	snp	C/T	1.65261e-05	0.0028745	intron-variant, missense, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20869832	CCTGCACGTCTTTCC[C/T]ATAAGAAATCTGATC	10529
rs148628803	snp	C/T	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:21094073	GAGTCTAAAAAAGAC[C/T]GGGCTGGGTGTGGTA	10529
rs148632920	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21000890	GGATGGCCAGGAAGG[A/G]CCACATTGGGATTTA	10529
rs148637703	snp	G/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20936390	AAATCAGCTGTTTAT[G/T]CCTAACAGGCTATTG	10529
rs148647782	snp	A/G	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:20904395	AAAAATCTTTGAAAC[A/G]TGTTTATGTTTTATG	10529
rs148647953	snp	C/T	0.00438332	0.0466095	intron-variant, upstream-variant-2KB	NEBL, LOC102725112	GRCh38.p7	10:20844135	TCAGCACATTACATA[C/T]TACAACACTGAATCA	10529
rs148669513	snp	G/T	0.0115144	0.0749975	intron-variant	NEBL	GRCh38.p7	10:20792612	TTCGAGACCAGCCTG[G/T]CCAATATGGTGAAAC	10529
rs148675827	snp	C/G	0.00438332	0.0466095	intron-variant	NEBL	GRCh38.p7	10:21036063	AGCTACTCAGGGAGC[C/G]GAGGCAGGAGAATCA	10529
rs148676091	snp	C/G	0.00159649	0.0282165	intron-variant	NEBL	GRCh38.p7	10:21105295	TACACCCATCAACTC[C/G]TCATTTACATTAGGT	10529
rs148687859	snp	C/T	0.0166325	0.0896639	intron-variant	NEBL	GRCh38.p7	10:20938253	AAACTTGCAGAGGAA[C/T]GATCAAGCAGCAACA	10529
rs148710363	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20892550	TTCCTGTTTTTACAG[C/T]CATCTGCACTCCTAC	10529
rs148714752	snp	C/T	0.00557542	0.0525036	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21146234	GCAGAGGGTACTCCG[C/T]TCACCCCTCTTACAG	10529
rs148718489	snp	A/G	0.0240643	0.107019	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20882799	CCTCTCTGGACTGCC[A/G]TCTAGTTTTTCAAAA	10529
rs148725524	snp	A/G	0.00398564	0.0444627	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21136296	CAAATACAACTGGCG[A/G]CTGTTGAAATCCAAG	10529
rs148744089	snp	C/G	0.00755907	0.0610114	intron-variant	NEBL	GRCh38.p7	10:21077974	CCGATGGATACTGCA[C/G]AGCTGGCTGTCACAG	10529
rs148752186	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20983283	AAAGATAGAACAATT[A/G]TCTTGAGACCATTTA	10529
rs148765147	snp	C/T	0.00835141	0.0640778	intron-variant	NEBL	GRCh38.p7	10:20835885	ATCTTCACTGACAAT[C/T]TTCTTTGGGGCTGGA	10529
rs148786098	snp	G/T	0.00517822	0.0506191	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20784844	ATCTCAAGCATCTTT[G/T]CAAAGTATGTTTTTC	10529
rs148789208	in-del	-/AA/AAAAAA			intron-variant	NEBL	GRCh38.p7	10:20803808	CTTCTGTACGAAAAA[-/AA/AAAAAA]TATATATATATATAT	10529
rs148789430	snp	A/T	0.0221141	0.102801	intron-variant	NEBL	GRCh38.p7	10:21118788	AGTTTCTCTTTCCTA[A/T]GAATGCATAGTCATT	10529
rs148791819	snp	A/C	0.0256215	0.110247	intron-variant	NEBL	GRCh38.p7	10:21029538	GGATACAGACAGGGA[A/C]GATCGTTCTTTTGGC	10529
rs148793989	snp	C/G	0.00597247	0.0543191	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20958659	CTTTATTTTAGAAGC[C/G]AAGTTCTTTTTCTTC	10529
rs148800166	snp	A/G	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21082734	TTATTTAAGAAGGGA[A/G]AATTATGGGATATGC	10529
rs148802432	snp	C/T	0.00438332	0.0466095	intron-variant	NEBL	GRCh38.p7	10:21018041	TGGCCAGGCTGGTCT[C/T]GAACTCCTGACCTCA	10529
rs148804254	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20928083	AAATTATTAATGGAA[G/T]AGTTTACATATTTTT	10529
rs148808962	snp	G/T	0.00557542	0.0525036	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20873072	TCAGGACCCGTTTCC[G/T]GTAACACTAGGTTTA	10529
rs148809325	snp	A/G	0.0103295	0.0711199	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20848541	GGTGAGCAAGGGTGA[A/G]GGAGCATTCCTGCCT	10529
rs148813678	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20922884	CTGAAAAATGTAAAA[C/T]GAAATGATAATACCA	10529
rs148814196	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20866637	GGCCTTCCCCTTGAG[G/T]AGAGTTTACTTCTCC	10529
rs148821465	snp	A/C	0.0205511	0.0992634	intron-variant	NEBL	GRCh38.p7	10:21111500	TGGGGAAAGGATGCC[A/C]TATTTAATAAATGCT	10529
rs148825535	snp	A/C	0.00953873	0.0683987	intron-variant	NEBL	GRCh38.p7	10:20827737	CCACAGAATACCATG[A/C]AGTCATAAAAAAGAA	10529
rs148825941	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21029986	AATGATAGACGTCCC[A/C]CGTCCCCCTCAAAGA	10529
rs148836188	snp	C/T	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:21010505	GCCATCCTCCCACCT[C/T]GAACTCCCAAAGCAC	10529
rs148851442	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21022154	ACACCTTTAGCTGCT[A/G]TGACCCCATGGTCAC	10529
rs148856703	snp	A/G	0.0441095	0.141807	intron-variant	NEBL	GRCh38.p7	10:20952865	AGCCGAGATTGCACC[A/G]CTGTACTCCAGCCTG	10529
rs148863316	in-del	-/C/CC			intron-variant	NEBL	GRCh38.p7	10:21029743	GCCCATGCCGGGATA[-/C/CC]TGGATCGATATGGCT	10529
rs148867903	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20871623	ACTTATAATCATGAA[C/T]CTGTCTGACAAGTGA	10529
rs148868526	snp	A/G	0.0142736	0.0832652	intron-variant	NEBL	GRCh38.p7	10:20805768	TGACGCAGGAGAACC[A/G]TTTGAACCTGGGAGG	10529
rs148874609	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21051960	GACAATCACTGGAGC[C/T]CAGGAGTTTGAAACC	10529
rs148875120	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21116644	TGGGTCACATTTTCC[C/T]GCTTCTTTGAATGCC	10529
rs148880427	in-del	-/GGGGGG			intron-variant	NEBL	GRCh38.p7	10:21165831	AACAGAAAAGTGGCT[-/GGGGGG]GTTATGATTCACAAA	10529
rs148891883	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21158367	TACAGTGTCTACTCT[A/T]TGTCAACTATTTACA	10529
rs148899177	snp	C/T	0.0134861	0.0810011	intron-variant	NEBL	GRCh38.p7	10:20997438	CCCCATCCCTACAGC[C/T]GCAAACCACACCAAA	10529
rs148906827	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20957267	GCTTATTAATGGGCA[C/T]ATAATTTATTTTACA	10529
rs148910799	snp	C/T	0.0410537	0.137264	intron-variant	NEBL	GRCh38.p7	10:20902213	TCGAGATCATCCTGG[C/T]TAACACTGTGAAACC	10529
rs148929575	snp	A/C	0.00398564	0.0444627	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20854148	TAGTAAATGGTAGCT[A/C]TTAAAGACTCAAGGC	10529
rs148935828	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21103661	TGGGTTTTTGTCTTC[C/T]TCCTGCTGAGTTTCA	10529
rs148944854	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21163550	TCCAACATTGGCAGG[A/C]AACCTTCTAACTCCC	10529
rs148950484	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21002043	TTGGGTTTTTCTACA[C/T]GTATTTCTTTTTCTT	10529
rs148950911	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20936951	TTCATCAAACATCCC[A/G]TTTTTTGCCTGGTAT	10529
rs148960508	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20905694	CAAAATGATGATAAG[G/T]CATCCAAAGAGCATT	10529
rs148964433	snp	C/T	1.77062e-05	0.00297536	intron-variant, missense, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20859801	TTATCCTTCATTTCA[C/T]TATCAAATTTTTCTT	10529
rs148968241	snp	A/T	0.0185938	0.0946107	intron-variant	NEBL	GRCh38.p7	10:20945446	GAGAATGGAGGAACA[A/T]GTAAAGTAAGCATAT	10529
rs148979994	snp	C/T	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21143803	AATACATCTAGATTT[C/T]CTATTCTAGGACTTA	10529
rs148982423	snp	A/G	0.00199481	0.0315187	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20857861	TTTTCATGCTACTGA[A/G]GGCGTACTAAATACA	10529
rs148990300	snp	A/T	0.0205511	0.0992634	intron-variant	NEBL	GRCh38.p7	10:21106591	TTGGTTACTATAGCC[A/T]TGTAGTATAGTTTGA	10529
rs148992539	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21037915	AGTAAGAACCATTTG[C/T]ATCTTCACCTCTGAA	10529
rs149022252	snp	C/T	0.0103295	0.0711199	intron-variant	NEBL	GRCh38.p7	10:20893688	GACAAGGGGATGATA[C/T]AGCAGTGTCTACAGG	10529
rs149030323	in-del	-/T			intron-variant	NEBL	GRCh38.p7	10:21017821	ACACTGATTCTTCTC[-/T]CTTTTTTTTTTTTTT	10529
rs149031327	snp	A/G	0.00676609	0.0577691	intron-variant	NEBL	GRCh38.p7	10:21080304	TCAAAACTCTGTGAA[A/G]ATTCCTCTTTTGATA	10529
rs149035468	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20799153	TTAGATTCATCGCAG[A/G]AATTTATTTATTTTA	10529
rs149041191	snp	C/T	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:21042266	TTTGGGACTGAGGAA[C/T]GTACGTCTTGGAGAG	10529
rs149042932	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20974466	GCCATGCTGCTTCTC[A/G]AACTCCTGAGGTGGG	10529
rs149075710	snp	A/G	0.00676609	0.0577691	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20898902	CTATTCTCCTAAAAT[A/G]TTGTGTTCTAGAAGG	10529
rs149083012	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21085174	GGACCCATTATATTT[C/T]TCACGCTCCATCACA	10529
rs149100000	snp	A/G	0.0209421	0.100162	intron-variant	NEBL	GRCh38.p7	10:21120319	GGTCAAGGCTACAGT[A/G]AGCTGTGATAGCACA	10529
rs149103332	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21031582	TGTTAACAGATTTGT[A/T]TAAGGAAGACCTCCT	10529
rs149113310	snp	G/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20992213	AAAATAGATATTACA[G/T]ATGTATATGAACATT	10529
rs149114420	snp	C/T	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:21019974	TTCAACACTTTCACC[C/T]GGAATTCCCACACAG	10529
rs149117657	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20931087	CACCTCAGTCATTCA[C/T]AATTTTCTCAACCTT	10529
rs149122869	snp	G/T	0.00438332	0.0466095	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20849758	TAGCAACACAAAATG[G/T]ACTAAAATATAAACT	10529
rs149123785	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20786710	AAGAAATTTCTGCAT[A/G]AGAAGCCAAGTATAA	10529
rs149153606	in-del	-/A			intron-variant, upstream-variant-2KB	NEBL, LOC102725112	GRCh38.p7	10:20844457	TCCCTTAATATAAAG[-/A]GTATATAAGCAGATT	10529
rs149153705	snp	G/T	0.0130921	0.0798413	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21126419	GAGAGAGAAACAAAA[G/T]CATTCCATATTTTCA	10529
rs149155361	snp	A/G	0.00755907	0.0610114	intron-variant	NEBL	GRCh38.p7	10:21034416	GACATTACTAATCAC[A/G]CCACTCTCAGCAGAG	10529
rs149161384	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20965418	AGGCCTCAAAGAGGG[A/T]GGAAGAAAGCCACAC	10529
rs149163458	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20887499	TCTTGGTTCGCTGCA[A/G]CCTCAACTTCCCAGG	10529
rs149168587	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20935017	CGATTTTATTTATTC[A/G]TTAAAACACTTACTG	10529
rs149173036	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20878960	TGGAAAGAGCCTCCC[A/G]GGGATCCGTGTAACA	10529
rs149176047	snp	C/G	0.00438332	0.0466095	intron-variant	NEBL	GRCh38.p7	10:20791440	ATGGGGTCTCACTCT[C/G]TCACCCAGGCTGTAG	10529
rs149180388	snp	A/T	0.00835141	0.0640778	intron-variant	NEBL	GRCh38.p7	10:20919059	ACTCATTTCAGAAAG[A/T]TTCCAAATGCCTTAA	10529
rs149192514	snp	C/G	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20823634	ATGATTATTTTCTAT[C/G]CAAAAATCAGTTTCT	10529
rs149197379	snp	A/G	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:21168054	TACTATACTTTGATC[A/G]TTCTATCAAAAGATC	10529
rs149198564	snp	C/T	0.0111196	0.0737302	intron-variant	NEBL	GRCh38.p7	10:21072939	GAGGTTGCAGTGAGT[C/T]GAGATCATGCCACTG	10529
rs149200918	snp	A/C	0.0228947	0.104514	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21140209	TGTATGGAATGGTTG[A/C]GAATCTGATATCTTT	10529
rs149214045	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20969362	ATTTCTAAGCTTTCA[A/G]TTAAACTTCCACTGC	10529
rs149249591	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21104883	GATGCCCGATATCAG[C/G]ATGAAGAAGTTTCCA	10529
rs149251564	snp	C/T	0.0111196	0.0737302	intron-variant	NEBL	GRCh38.p7	10:21171779	TTACCTTTTTTAATC[C/T]CCACCTACTACAGCA	10529
rs149263265	snp	A/G	0.0111196	0.0737302	intron-variant	NEBL	GRCh38.p7	10:20937853	ATTGCTAGCACAGCA[A/G]TCTGAGATCAAACTG	10529
rs149264293	snp	A/G	0.00914312	0.0669923	intron-variant	NEBL	GRCh38.p7	10:21003599	AACCAACTCTATTCA[A/G]TCAATGATTATTGAC	10529
rs149267205	snp	A/G	0.0107246	0.0724382	intron-variant	NEBL	GRCh38.p7	10:20917037	AGTGAAAGGGACTGT[A/G]TACTGAAAAAAAATA	10529
rs149268230	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20860774	CATCTAAAGGCTCTG[C/T]TTTGCAGAAGACTTT	10529
rs149279206	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20821508	TAAATACTACAAATA[A/G]CACCTACAATGTTAT	10529
rs149287609	in-del	-/TAAAG	0.0505692	0.150756	intron-variant	NEBL	GRCh38.p7	10:21085742	GAAGTGTATATGTGT[-/TAAAG]TAAAGTTTTGTTCTA	10529
rs149292132	snp	C/T	0.0142736	0.0832652	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21145329	GTTATTTGTATAAAG[C/T]TGTTCAATGCAGCAC	10529
rs149300648	in-del	-/G	0.0134861	0.0810011	intron-variant	NEBL	GRCh38.p7	10:21060326	ATTCAAAACAAAAGA[-/G]GGGGTTTCATTTTCA	10529
rs149301475	snp	A/G	0.0205511	0.0992634	intron-variant	NEBL	GRCh38.p7	10:21107597	GAGGATTTTTGCATC[A/G]ATGTTCATCAAGGAT	10529
rs149307370	snp	C/T	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:21039295	TTAGTCATGAAGTCT[C/T]TGCCTATCCCTATGT	10529
rs149310273	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20947621	TTCATAGTTGTTTAT[C/T]ATCATTGTGCCAGGC	10529
rs149321738	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20863468	ATCAATCCCCAGCAA[A/T]CTTGGATGAAATCAA	10529
rs149323613	snp	C/G	0.00597247	0.0543191	intron-variant	NEBL	GRCh38.p7	10:20799898	GTTACTATAGTGAAG[C/G]AAATTATCATACCTA	10529
rs149338180	snp	A/C	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:20895537	AGCTGCAATCCCTGG[A/C]ACACAATAGTCACTA	10529
rs149341574	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20808063	CTGTCTGCAAGTTTA[C/T]ATTAATATTTAAAAT	10529
rs149345768	snp	C/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21151032	AATTCCCTGACCTCT[C/G]AGCATCACTGAAAGG	10529
rs149347586	snp	C/T	0.00597247	0.0543191	intron-variant	NEBL	GRCh38.p7	10:21055833	TGTTCAGGGGGCTCC[C/T]GCGTGAGAATGAAAA	10529
rs149349283	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21082513	AAATTTTTTGTAAGT[C/T]TGAAGTGTTCCCCAC	10529
rs149359593	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21045269	GATGAAATCTGACCA[C/T]TCAAGTATTGAACAA	10529
rs149360821	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20950732	GATCAAGAAATGCCA[C/T]TTATCATCAAAGGCC	10529
rs149364004	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21096010	CTGGCTCTAACATTC[A/G]AAATGTAACATTACA	10529
rs149370808	in-del	-/CCCCCC			intron-variant	NEBL	GRCh38.p7	10:21019324	ACTGGCCTAAGGCCA[-/CCCCCC]CAGCCAATGAACAGA	10529
rs149380192	snp	C/T	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20988831	ACATTGCTAAATCCA[C/T]TGGGCAATTCTGCCA	10529
rs149384673	snp	C/T	0.0023933	0.0345097	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20846112	CTCTTTGGCTATGAC[C/T]CTCTAAATTCTAACA	10529
rs149398468	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21087239	CAACAATAAATATTT[G/T]CTCACTAAATAAATG	10529
rs149422393	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21120739	GAGTGTTAGAGTGAA[A/G]AAGTTCCCTGTGGAG	10529
rs149423100	snp	A/G	0.00557542	0.0525036	intron-variant	NEBL	GRCh38.p7	10:21033130	AAGGAAATGTGTGAC[A/G]TCGAGCAGCCCTGTG	10529
rs149428942	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20884305	TGGTCTTCAACTCCC[A/G]GGCTCAAGAGATCTG	10529
rs149433032	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20994076	AATGTTACATAACTC[A/C]AATTACTGAACCTCA	10529
rs149441387	in-del	-/T	0.030278	0.119257	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21132622	TGTGTGAGAGTTCCA[-/T]TTTGTCCACATTCTC	10529
rs149458013	snp	A/G	0.0689305	0.172377	intron-variant	NEBL	GRCh38.p7	10:20894731	CATCCTAACTAACAC[A/G]GTGAAACCCCGTCTC	10529
rs149463297	snp	C/T	0.00318978	0.0398085	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21138171	TAGAAACCAAAACAG[C/T]CTTATATTATTGGGA	10529
rs149472285	snp	C/T	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:21035631	GAGAAAGATGTCCAG[C/T]TTTAAGCCTTTTCCA	10529
rs149474674	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20967357	ACAGGGCTGGGCATG[A/G]TGGCTCACGCCTGTG	10529
rs149481807	snp	C/T	0.0138799	0.0821421	intron-variant	NEBL	GRCh38.p7	10:20889271	CAACATAAACTGTAG[C/T]TCTAAATGCTCTCAG	10529
rs149482445	snp	G/T	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:20825412	CTGTAATCCCAGCAC[G/T]TTGGGAGGCTGAAGC	10529
rs149486641	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20936315	TACTCTATTTCCTAC[A/G]GTAAAAGGGGCAATA	10529
rs149490493	snp	C/T	1.64923e-05	0.00287156	intron-variant, synonymous-codon, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20869794	GTCTGGTCGGTCAAG[C/T]TCTGCACTGTACGTG	10529
rs149492506	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20792524	TGTCTAGTCCTGGCC[A/G]GGCATGGTGGCTCAC	10529
rs149511519	snp	C/T	0.00478085	0.0486577	intron-variant	NEBL	GRCh38.p7	10:20802750	CAATCAGAACTTACT[C/T]GAAAGAAGGAACGAA	10529
rs149514665	snp	C/T	0.0205511	0.0992634	intron-variant	NEBL	GRCh38.p7	10:21074668	TACTTTCAGTAGAGA[C/T]GGGGTTTCACTGTGT	10529
rs149515290	snp	C/T	0.00199481	0.0315187	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21142279	TGACTTCACCCTGGG[C/T]TGCACCAGCCCTGTC	10529
rs149522882	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20978075	CTCTGGGCTCCTAAC[A/G]CTTCAGGAAATACTG	10529
rs149550279	snp	G/T	0.00199481	0.0315187	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20868481	TTATGCTTAAAATTA[G/T]ACTTAATTTTTTTCC	10529
rs149554039	snp	A/G	0.0123036	0.0774623	intron-variant	NEBL	GRCh38.p7	10:20842018	TTGCGTATGAAAATC[A/G]TAAATATCTTATTCC	10529
rs149557616	snp	A/G	0.0146672	0.084371	intron-variant	NEBL	GRCh38.p7	10:21113583	GGCTGTCCTTTTTAT[A/G]ATGCAGAGTGAGAAC	10529
rs149565951	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21077836	GGGGTCAACATTGTC[A/T]GGCACAGCAGAACTG	10529
rs149572307	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21012319	ATGATTTATGTGAGA[C/G]AAAGATGAAAAATGC	10529
rs149574547	snp	C/T	0.0256215	0.110247	intron-variant	NEBL	GRCh38.p7	10:20924768	AACACTGTAGAGCTT[C/T]CCCCATAGAAAGAGA	10529
rs149590364	snp	C/T	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:21025238	AAATATGACATGTAA[C/T]GCATTCAGAGCTGGT	10529
rs149590976	snp	C/T	0.00597247	0.0543191	intron-variant	NEBL	GRCh38.p7	10:20954652	CCCCTGCTAGAGAGC[C/T]TCCTGCCTCATAGTT	10529
rs149596017	in-del	-/AC	0.0490535	0.14873	intron-variant	NEBL	GRCh38.p7	10:21033010	AGGTGAGAAATTAAT[-/AC]ACACACACACACACA	10529
rs149602977	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20872836	TCAGGCCGGTACCCT[A/G]CATGGTCTAAAAAGG	10529
rs149607328	snp	A/G	0.0023933	0.0345097	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20784609	CCAGATCATCTCTGT[A/G]TGGAATTGGTAACTT	10529
rs149620381	in-del	-/CCT	0.222928	0.24853	upstream-variant-2KB, nc-transcript-variant	NEBL, NEBL-AS1	GRCh38.p7	10:21174563	CCAGGGTGCGCCCTC[-/CCT]CCTCCTCCAGCCAGT	10529
rs149629151	snp	A/G	0.00438332	0.0466095	intron-variant	NEBL	GRCh38.p7	10:21066307	AAATGTTAATTATTG[A/G]TGAATTTTTCATGAA	10529
rs149630841	snp	A/C	0.131038	0.219882	intron-variant	NEBL	GRCh38.p7	10:21000218	GGGGTATAGAGGGGG[A/C]ATGGGGGGCCAGAGG	10529
rs149635643	snp	C/T	0.00557542	0.0525036	intron-variant	NEBL	GRCh38.p7	10:20912606	GTCTTTATCTCTTGC[C/T]GGCCTCTAGGTCATT	10529
rs149643565	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20958564	TCAATTTCATAAGCA[A/C]CCAAACCCCATCTGA	10529
rs149644898	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20903850	CATAGAGTACTGTAA[C/T]GGCCAATGGAGACTC	10529
rs149647815	snp	A/C/G	0.00014907	0.00863231	intron-variant, missense, stop-gained, nc-transcript-variant	NEBL	GRCh38.p7	10:20831228	ATGTCCTCTTGGCTC[A/C/G]AAGGATATCTGGGAT	10529
rs149649244	snp	C/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20816360	ATGGTCGTGGTTTCT[C/T]AGGAATTAACTGCGG	10529
rs149655456	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20809735	ACAGTACAATGAACC[C/T]CTACAGTTCACAGTG	10529
rs149663858	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20991021	CAACAAATTAGCATC[C/T]CTAACACATACTCTG	10529
rs149676446	snp	C/T	0.0103295	0.0711199	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20898186	TAAAAAAAAATTTCT[C/T]AAAACAAATATTTTA	10529
rs149694745	snp	C/T	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:20906864	CTCTAACTTTCTCTC[C/T]TATTTCAATCATACA	10529
rs149698639	in-del	-/A	0.0130921	0.0798413	intron-variant	NEBL	GRCh38.p7	10:21003954	AACCAAAAGTCGTCC[-/A]AAAAAATCAAGAATC	10529
rs149703726	snp	C/T	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:21098308	AAGGAGACATTTTCA[C/T]GCATCCACACAAAAG	10529
rs149705806	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21165636	TGCCCAATCTCGTCT[A/G]CGTGCCAGGCTTGGG	10529
rs149706969	snp	G/T	0.00119737	0.0244387	intron-variant, downstream-variant-500B	NEBL	GRCh38.p7	10:20815155	TGTACACCACTGGAC[G/T]TTGGTGAGCAACTGA	10529
rs149718922	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20997044	TTTCAAAAATCCATC[C/T]TTCTACACTGTAACT	10529
rs149735449	snp	C/T	0.00835141	0.0640778	intron-variant	NEBL	GRCh38.p7	10:21033533	CTCTCAAAATTCATC[C/T]ATGTAGAACAGAAAT	10529
rs149737043	snp	A/C/G	0.000265213	0.0115128	intron-variant, missense, stop-gained, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20852649	GCTTTTTATATTCTC[A/C/G]CTAAAATACAGAATG	10529
rs149737880	snp	G/T	0.0532157	0.154195	intron-variant	NEBL	GRCh38.p7	10:20941173	CCTGATGAACATTGA[G/T]GCAAAAATCCTCAAT	10529
rs149746748	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20934408	TGCACTAACGCAGAC[C/T]CATTAGTCATTCTCC	10529
rs149749478	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20853616	AAAATAGTGAGACCC[C/T]AGTTCTACAAAAAAT	10529
rs149755451	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21102842	TTTATTTTTATTTTT[A/G]TAGTTCCAGGGTACA	10529
rs149773584	snp	A/C/T	0.00119737	0.0244387	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21139558	AGCCTCATGTTGTCA[A/C/T]AGCAATGATGAAATG	10529
rs149786468	snp	A/C	0.00676609	0.0577691	intron-variant	NEBL	GRCh38.p7	10:20968688	AATATGTTTAACAGA[A/C]GCCTAAAATCTCAGG	10529
rs149787587	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21037504	AAAATAAAAATATAT[A/G]TGTTGAAATTAGTGG	10529
rs149791668	snp	A/G	0.00517822	0.0506191	intron-variant	NEBL	GRCh38.p7	10:20944793	AATTGGCATTGCTTC[A/G]ACATACAGAGATACA	10529
rs149793273	snp	C/G	0.00835141	0.0640778	intron-variant	NEBL	GRCh38.p7	10:20890740	CCAGAATTGTTATGC[C/G]GGGGGAAGACCCGGG	10529
rs149803458	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20857674	TGCAGGACTGACCAC[A/G]TGGGCAGTGCACCCA	10529
rs149804343	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20793991	CCCCAATTCCCTCTT[G/T]TCCCCCAGTGCTTTG	10529
rs149814553	snp	A/G	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20838933	CAGTATGGTATAAAC[A/G]TAACATGTATATGTA	10529
rs149821906	in-del	-/ATATATATATATATATAT			intron-variant	NEBL	GRCh38.p7	10:20896484	ATAAATATTATATGC[-/ATATATATATATATATAT]ATATATATATATATA	10529
rs149827535	snp	C/T	0.0221141	0.102801	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21143477	AAAAAAAAAATCAAA[C/T]GTGAAAAGTGCTTTA	10529
rs149830160	snp	C/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21075941	AAAGATGTTCTACAT[C/G]AAGAATCATTAGGGA	10529
rs149846972	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20830295	ATCAAATTAAATGCT[A/G]TGGTCAATTTTAAAT	10529
rs149865408	snp	C/G	0.00676609	0.0577691	intron-variant	NEBL	GRCh38.p7	10:20843299	AGTCTCCAGAACTTT[C/G]AGAAAAGTCTGTTGG	10529
rs149868956	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21115615	CAAGGAGTTCGCTCA[A/G]TATCACCTTTGTTCT	10529
rs149868974	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20780577	ATTATTAGGGTGCAT[C/T]GCTTGCATCTAACAA	10529
rs149872097	snp	A/G	0.00716266	0.059414	intron-variant	NEBL	GRCh38.p7	10:21093477	ATCAGTCCCTCCATC[A/G]GCACTGAAAAAATCC	10529
rs149877659	snp	A/T	0.00597247	0.0543191	intron-variant	NEBL	GRCh38.p7	10:21026561	ATTATATCCATCTCC[A/T]TCTTCTCCCTCCTGA	10529
rs149878829	snp	C/T	4.94262e-05	0.00497098	intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20819453	CCTGGTTTCGCCTCA[C/T]TCTCTCTATCTCCGG	10529
rs149879516	snp	C/T	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:21078732	TACAAGATCATTCTC[C/T]CTATATCCACCCTAG	10529
rs149886987	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20925812	GAAAATCTGGACATA[C/G]AGCTTTCTCTAATTA	10529
rs149887562	snp	C/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20985239	AAAAAGGTTGGTGAC[C/T]GCTATGGTGAAGAAA	10529
rs149908128	snp	G/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20879694	GGCAACTGTACTTCA[G/T]GTACTTTTCCAAGAA	10529
rs149915861	snp	A/T	0.00557542	0.0525036	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21128470	TGGAAGGAATGACAC[A/T]CTGAGCCACATAACC	10529
rs149920825	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20786150	AAAGTCACTAAATAC[A/G]ACAGGTAGCCCATCA	10529
rs149929630	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21031253	CTATGGGGGTCACCC[A/G]TCACCTGCTCACCAT	10529
rs149930196	snp	C/T	0.00953873	0.0683987	intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20959927	ATTAATACATACCTG[C/T]GTGATAAGGGTATTT	10529
rs149940445	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20930645	TGACACACCATCCTC[C/T]TTTTCACTGCAGAAC	10529
rs149946391	snp	A/G	0.0364509	0.129988	intron-variant	NEBL	GRCh38.p7	10:21067122	GGACTACAGGCGCCC[A/G]CCACCACGCCCGGCT	10529
rs149946753	in-del	-/T			intron-variant	NEBL	GRCh38.p7	10:21058801	ATAATTTAGTTCATT[-/T]CAGAACCAATTCTGA	10529
rs149950674	snp	C/T	0.00517822	0.0506191	intron-variant	NEBL	GRCh38.p7	10:20972415	AGAAGAAAAAAACTC[C/T]GTAAACAGCAAAAGA	10529
rs149952543	snp	C/G	0.0103295	0.0711199	intron-variant	NEBL	GRCh38.p7	10:20913882	TGTTCAAAAACTGGA[C/G]TTTTCTTTTTCAGGC	10529
rs149961632	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20882156	TGGGTGATAGAGCAA[A/G]ATCCTGCAAAAGAAA	10529
rs149963811	snp	C/T	0.0126979	0.078662	intron-variant	NEBL	GRCh38.p7	10:20819603	TTTTTAAATGTCACA[C/T]GGCTACAGAACATTC	10529
rs149965221	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21162739	TGATAGGTGATATAA[C/T]TGAGGCATAAAAAGT	10529
rs149966925	in-del	-/A	0.0295035	0.117819	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21139178	ACATAGCACTAGTGG[-/A]ACTTTTTCTGGGAAT	10529
rs149969003	snp	C/T	0.00199481	0.0315187	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21135620	AAGAAACAGCTCCTA[C/T]GGGTGCACCAAATCT	10529
rs149985087	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB, nc-transcript-variant	NEBL, NEBL-AS1	GRCh38.p7	10:21174485	TCTCTTCCCCAGCCG[A/G]GGGCACCCTCATCCC	10529
rs150000482	snp	G/T	0.000115436	0.00759637	intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20889889	CATGGTTTAGCATAG[G/T]ACTGTCAGTCACAAA	10529
rs150002129	snp	A/G	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20918790	CGGGAGGTAGAGCTT[A/G]CAGTGAGCCGAGATT	10529
rs150005921	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20861944	ATCACAGCTTCGCCT[A/G]GCCTACCTTAAACAT	10529
rs150020783	snp	A/G	0.00716266	0.059414	intron-variant	NEBL	GRCh38.p7	10:21072852	AAAAGTTAGCCAGGC[A/G]TGGTGGCAGGCACCT	10529
rs150025642	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20806864	ATTGCCTTTGGGAGA[G/T]ACATCAATTCCAGTA	10529
rs150028940	in-del	-/C	0.0383715	0.133092	intron-variant	NEBL	GRCh38.p7	10:20995890	GTACCCACCAACTTA[-/C]CCTTTGTGGGACTAA	10529
rs150037266	snp	C/T	0.0142736	0.0832652	intron-variant	NEBL	GRCh38.p7	10:21108467	TTCCACATAGTTGTG[C/T]GCTTTTGAGGGAGTT	10529
rs150044436	snp	G/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20948456	ATCAAGTAAATAATG[G/T]CTTACCCTTCACAGT	10529
rs150055622	snp	C/T	0.00318978	0.0398085	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20866479	TATACTCAAAATCAA[C/T]ACACATTGACCCATT	10529
rs150081398	in-del	-/AT			intron-variant	NEBL	GRCh38.p7	10:20929260	ATGTGAGAGATATAA[-/AT]ATATATATATATATA	10529
rs150094100	snp	A/G	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:21048059	TATCAACACATTGCA[A/G]TGCAAAGTGAGCGGT	10529
rs150103686	snp	C/T	0.00597247	0.0543191	intron-variant	NEBL	GRCh38.p7	10:20946712	AGTCCCGTTTTATTA[C/T]TCTTTAAACTGGACA	10529
rs150105145	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20892184	ACAAGCTGATCTAAA[C/G]CAGGCATGGTCATGC	10529
rs150110895	snp	C/T	0.0275645	0.114116	intron-variant	NEBL	GRCh38.p7	10:20805718	ATTAGCCAAGTGTGG[C/T]GGCGTGCACCTGTAA	10529
rs150112240	snp	A/T	0.00279162	0.0372561	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21145073	TGGATAGAACAAGAA[A/T]CCAAAAATAACACAA	10529
rs150132407	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21157876	GTGTCCTTAGAAAAC[A/G]AGATTAGGACACAGA	10529
rs150136407	snp	C/T	0.00676609	0.0577691	intron-variant	NEBL	GRCh38.p7	10:21090479	GATGCGTGTAGGTTA[C/T]ATGAAAACACTTTGC	10529
rs150144520	snp	C/T	0.00993419	0.0697739	intron-variant	NEBL	GRCh38.p7	10:20982013	TAGCATTAAAACATA[C/T]CTCAATGGGTTTTAG	10529
rs150146074	snp	A/G	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:21051746	TTAAATGTCCTAACT[A/G]TATGTTATCTACAGG	10529
rs150151992	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20902170	GCACTTTGGGAGACC[A/G]AGACAGGCGGATCAT	10529
rs150152264	snp	G/T	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20840105	CACCATCGTCATCGC[G/T]ATCATCATCATCATT	10529
rs150152361	snp	C/G	4.96339e-05	0.00498142	intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20809829	ATATGGAGACTTCTA[C/G]ACTGAATATTGTCTT	10529
rs150180427	snp	A/T			utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20783790	TCAGTTTATTTTTGT[A/T]GGTTTGTGTACAATA	10529
rs150184985	snp	C/T	0.00835141	0.0640778	intron-variant	NEBL	GRCh38.p7	10:21095562	GATTTTGAAGCTAAT[C/T]GGATTATTTAGGATG	10529
rs150189554	snp	A/C	0.021333	0.101051	intron-variant	NEBL	GRCh38.p7	10:21027961	GTGCAGTGGCTCACA[A/C]CTGTAATCCCAGCAC	10529
rs150192061	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20936851	TGAATAAGCTTGGGT[C/T]GATTCCTTTTCAGCA	10529
rs150199531	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20988610	AAATTGTCTCTCTCT[A/G]TTGGGTCACTGCCAT	10529
rs150200844	snp	C/T	0.0154538	0.0865337	intron-variant	NEBL	GRCh38.p7	10:20926706	GAGAGTGTGTCGTCT[C/T]GCATTCAGCAATGGC	10529
rs150205442	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20846028	AACAAGAAATGAAAG[A/G]TGGATGCGACGGTGA	10529
rs150225871	snp	C/T	0.00597247	0.0543191	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21132631	GTTCCATTTTGTCCA[C/T]ATTCTCACCAACATT	10529
rs150232879	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20788093	TGTTTTGAAGAACTC[A/G]GAATTCTAGAGAAGC	10529
rs150241602	snp	A/C	0.00636936	0.0560724	intron-variant	NEBL	GRCh38.p7	10:21033025	TACACACACACACAC[A/C]CCTACATATTGTTTA	10529
rs150258455	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20974184	CTTTGCTCTTCCCAT[C/T]CTATCATGCTACAAA	10529
rs150262040	snp	C/G	0.0256215	0.110247	intron-variant	NEBL	GRCh38.p7	10:20915811	GTATTTCTAGTTCTA[C/G]ATCCCTGAGGAATCA	10529
rs150275086	snp	A/C	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20820454	GGACAGTTTTAGTGT[A/C]TTTTTAGACTTTAAA	10529
rs150276039	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20798829	TGAATCTTGGCACAT[C/T]GATGAAAGACACATG	10529
rs150283828	snp	A/G	0.00835141	0.0640778	intron-variant	NEBL	GRCh38.p7	10:21069089	AGACAGTGTCTCACT[A/G]TGTGGCCCAGGCTGG	10529
rs150297259	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:20798108	ACCCTGTTTCTAATT[-/A]ACAAAAAAAAAAAAA	10529
rs150300572	snp	C/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21014524	TCTTTGGACAGTCAA[C/T]GGAGTTCTTCAGTCA	10529
rs150315229	snp	A/G	0.0115144	0.0749975	intron-variant	NEBL	GRCh38.p7	10:20919997	CAACCCAATATGGAC[A/G]AAAGATGAATAGTTC	10529
rs150317563	snp	G/T	0.030665	0.119967	intron-variant	NEBL	GRCh38.p7	10:20836428	AGGTTTCACCACGTT[G/T]GCCAGGCCGGTCACG	10529
rs150326806	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20825143	TTGAAGTATACTTTA[C/T]TATTGCATTCTCTTA	10529
rs150335748	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21074387	TAGAAACTAATATCA[C/T]CCACTTCACAGAGGA	10529
rs150345963	snp	C/T	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:21054338	GCCAAATCTGTTTAA[C/T]GGTTATTTTTCCCAG	10529
rs150356409	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21019835	TTTAAATATTTAGGA[A/C]CAAATAAGTCAAGAT	10529
rs150357967	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20950161	AGGCTAACTACAAGC[C/T]GCAGGGCATCGGGGG	10529
rs150358534	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:20981093	TGTGCCCAGCCCCAA[-/A]CAAATTATTTATTCA	10529
rs150360306	snp	C/T	0.0107246	0.0724382	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20874988	AAGTGATCCTCTCAC[C/T]TTGGCCTCCCAACGT	10529
rs150389866	snp	C/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21155416	CATTAACATCCCCAC[C/T]TCCTCACCACCCTCC	10529
rs150397150	snp	A/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20993116	TAGGGAGTTTTTCAA[A/T]GTCTTTTTAAAACAA	10529
rs150397941	snp	A/T	0.021333	0.101051	intron-variant	NEBL	GRCh38.p7	10:21060604	TTATCTCATTTTTTT[A/T]AAAAATCCCCTGGAA	10529
rs150399419	snp	A/G	0.00438332	0.0466095	intron-variant	NEBL	GRCh38.p7	10:20965296	ATGTTAGTGGGAAGC[A/G]CTAAGAGAGAAAAAT	10529
rs150408264	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20954372	CTAGGCCCTGGGTCT[A/G]TATAGAAAAAAAGAC	10529
rs150412104	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20899740	ATAAATGTTGTTATG[A/C]CAGGCACTGTGCTTG	10529
rs150413689	snp	C/T	3.38989e-05	0.00411683	intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20828583	TTTCAGGAGTATCTG[C/T]TATGGTAGAATAGTT	10529
rs150413888	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20878835	GCTTTATACTCTATT[C/G]CCTCAATCCCTCAAT	10529
rs150415348	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20811643	TACTTAGTGCTGCTC[C/T]GACTTTAGCACCCTG	10529
rs150430383	snp	C/T	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:20908059	CTCCACTGACCTATA[C/T]CAGGTACCGAGAAAA	10529
rs150437990	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21167389	AATGTAGGCAGGTCA[C/G]AGGAAATGTTCAGCC	10529
rs150449588	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20999269	TATGTGTGAGAAGAC[C/G]TGCAGTGATGCTATA	10529
rs150454615	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20911942	GTTGCAAAAATTTCT[C/T]GGCAGTTTGACTCAA	10529
rs150468221	snp	C/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20816205	ATAAGAGAGTACATG[C/T]GTCCAAATCACTGTG	10529
rs150472307	snp	G/T	0.0267878	0.112589	intron-variant	NEBL	GRCh38.p7	10:21010284	AGGTATAGCTCTGTC[G/T]ACCAGGCTGGAGTGC	10529
rs150480036	snp	C/T	0.0103295	0.0711199	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21140837	AGGACAAATATCTAA[C/T]GCATGCATGGCTTAA	10529
rs150480345	snp	A/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20802071	GAAAACAGAAACACA[A/T]AGCATACCTGAAGCA	10529
rs150485878	snp	C/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20855618	AGTCTCTGCTACCTC[C/T]TAGTGGGAGATACAC	10529
rs150490702	snp	G/T	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:21104706	TCTTTTCTAATCTGT[G/T]TGCTTTTTATTACTT	10529
rs150493006	snp	C/T	0.0119091	0.0762411	intron-variant	NEBL	GRCh38.p7	10:21035142	TAGCTGGATTGCAGG[C/T]GCCTGCCACCACGCC	10529
rs150500265	snp	A/G	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:21030325	AGGAAGTGAGTCATC[A/G]CACACTGGGACCTCC	10529
rs150507525	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20937525	GAGTGACGCAGAAAA[C/T]AGATGATTTCTGCAT	10529
rs150510299	snp	C/T	0.00676609	0.0577691	intron-variant	NEBL	GRCh38.p7	10:20990756	ACATTTTTCTTTCTG[C/T]CTCACCCAGTGTGAC	10529
rs150513051	snp	A/G	0.0130921	0.0798413	intron-variant	NEBL	GRCh38.p7	10:20928734	CTTCTCTAGAACTTT[A/G]CTCCTGCTGTAATCC	10529
rs150518025	snp	C/G	0.00358779	0.0422022	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20848952	TCAACAAATAGCATA[C/G]TTAATGCTTACAAAA	10529
rs150518045	snp	C/T	0.000660142	0.0181559	intron-variant, missense, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20852559	CCTGACTTTGGAGGA[C/T]GGCATTGCCTTTATG	10529
rs150540073	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20796447	TAAATATTGAAAAAA[A/C]ACACAACATTAGTTG	10529
rs150545228	snp	A/C	0.00358779	0.0422022	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21134302	ACAGTTGAATTAAGT[A/C]ATGTCCTACTCTCCT	10529
rs150555447	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21033345	TAAGTATCATACCTA[C/T]AGCAAATGTGCAATA	10529
rs150572829	snp	A/G	0.0295035	0.117819	intron-variant	NEBL	GRCh38.p7	10:20790422	AGCCTAGCCAACATG[A/G]TGAAACCATCTCTAC	10529
rs150580534	snp	A/G	0.0134861	0.0810011	intron-variant	NEBL	GRCh38.p7	10:20895235	CAAGTTAGCTCAGCT[A/G]TAATTGCACTTCAAT	10529
rs150581139	snp	A/G	0.00557542	0.0525036	intron-variant	NEBL	GRCh38.p7	10:20833830	GGTTAGGAAGCTATG[A/G]CAATGATCTAGAGGA	10529
rs150591638	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20799802	CTAAATCAGGAGTGT[A/G]TTTTCTTCTTCTTAA	10529
rs150592437	snp	A/G	0.0111196	0.0737302	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21139266	ATTTTCATTAGCATG[A/G]AGCTTTGGAGTTGTG	10529
rs150599785	snp	G/T	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:20975388	TTTCATAGTTCATGA[G/T]AGTACAGCTATTTGA	10529
rs150600426	snp	C/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21044890	GAGGAGGAGAATTGA[C/T]AAAAATACTTAATGA	10529
rs150608690	in-del	-/C			upstream-variant-2KB	NEBL	GRCh38.p7	10:21175655	ATTCACCAAATTCAA[-/C]CAGCCCCTGAGCCAC	10529
rs150616905	snp	A/G	0.00795532	0.062565	intron-variant	NEBL	GRCh38.p7	10:21081139	GGAATACAGGCATGA[A/G]CCACCACACCTGGCT	10529
rs150628563	snp	A/G	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:20921608	GACTTCCTGAATCTC[A/G]GGGCACCTCACTATC	10529
rs150634204	snp	A/G	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:20838550	ATTTAGGATACTACA[A/G]AAACTTTGTCATTAA	10529
rs150638783	snp	A/G	0.00676609	0.0577691	intron-variant	NEBL	GRCh38.p7	10:21086850	ATGACAAAGACAGAT[A/G]CCAGTTTGCTGAAGA	10529
rs150639411	snp	C/T	0.00676609	0.0577691	intron-variant	NEBL	GRCh38.p7	10:21110683	TATGCCACCACCCCA[C/T]GGAAGGCTCAGTGGA	10529
rs150651116	snp	C/T	0.00636936	0.0560724	intron-variant	NEBL	GRCh38.p7	10:20980115	AGAAATTCCATAGGG[C/T]TTGTATTCAAAGAAC	10529
rs150654596	snp	C/G	0.0162398	0.0886349	intron-variant	NEBL	GRCh38.p7	10:21122160	CCTGCCAAGTAGCTG[C/G]GATTACAGGCACCTA	10529
rs150667007	snp	A/G	0.0154538	0.0865337	intron-variant	NEBL	GRCh38.p7	10:21021250	CATTTTTTAATTGTC[A/G]GCCACATTTATCGTT	10529
rs150672283	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20932587	CCAGAACTTAAAGTA[A/T]AATTTTTTTAAAATT	10529
rs150676143	snp	C/T	0.000153988	0.00877328	intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20817604	GATGATCACACATTG[C/T]TGATGTTTTTCTGGT	10529
rs150676602	snp	C/G	0.00597247	0.0543191	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20876950	TTGGCTGTTTTTAAT[C/G]ATTTTCTGATTATAG	10529
rs150687182	snp	C/G	0.00279162	0.0372561	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20780331	TTGAGGACATATGAG[C/G]AATTTATTCTTGAAA	10529
rs150707205	snp	C/G	0.000798403	0.0199641	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21127893	TTGCAATTTGCAATT[C/G]AAAGAGATAACCAAT	10529
rs150712173	snp	C/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21062084	GAAGATTCTAGTCGT[C/G]TTCTGTGTGTACACA	10529
rs150713071	snp	C/T	0.0402882	0.136092	intron-variant	NEBL	GRCh38.p7	10:20967167	TGTTCTTAATAACGT[C/T]GTTTCTATTTTCAAA	10529
rs150715784	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20910068	CTCAGGGTAGGACTC[C/T]ACTTTAAAAAGTTGA	10529
rs150721357	snp	A/C	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:21025935	TCACTATTACTATTA[A/C]TATTATGGCTACTAA	10529
rs150723624	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20955449	ATTTACAGATAGTGT[A/G]AAATTGTCCTAAACA	10529
rs150726180	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20879576	CAAATAACAGTTGCC[A/G]TTCTGCGGAAAACAC	10529
rs150729189	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20812568	CCAATAATAGAAAAG[A/G]CTTGAGATGATACCA	10529
rs150750126	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21169522	GCAATCCATACTGCC[C/T]AGCCAGTTTACATGG	10529
rs150755700	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21007098	ATGAGAGGAGAAAGC[C/T]GAATGAAATACAGAA	10529
rs150764117	snp	C/T	0.0217236	0.101931	intron-variant	NEBL	GRCh38.p7	10:21067063	CTGAAAGCTCCGCCT[C/T]CCGGGTTCACGCCAT	10529
rs150769296	snp	C/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20913318	GCACTGCCGATCCTT[C/G]ACATTGAACATCAGA	10529
rs150770309	snp	C/T	0.00398564	0.0444627	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20856585	AGCATATCTATGAGT[C/T]GTGGAGAAAAAAGAC	10529
rs150790727	snp	C/G/T	0.0023933	0.0345097	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20868098	ACAGAAGTTGCATGA[C/G/T]GTTTATATAATTCTG	10529
rs150794885	snp	A/G	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:21113026	GCCACTCCTGAAGAA[A/G]AAGGAGGAGGAGAGG	10529
rs150803707	snp	A/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	NEBL, NEBL-AS1	GRCh38.p7	10:21174475	CCCTCCCTCTTCTCT[A/T]CCCCAGCCGGGGGCA	10529
rs150811035	snp	A/C	0.00795532	0.062565	intron-variant	NEBL	GRCh38.p7	10:21011689	TTGGCATCTGTTGGC[A/C]TCTGTGGCTGGTAAC	10529
rs150841195	snp	A/C	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20892676	CACCCACAAATCCCA[A/C]GTCTCCATTACAATT	10529
rs150843894	snp	A/G	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20806266	AAGCAGAGGCCCTCC[A/G]AATTCCTGATCTCTA	10529
rs150845080	snp	C/T	0.000763308	0.019521	missense, intron-variant	C10orf113, NEBL	GRCh38.p7	10:21146393	GAAAAAAATGACTGG[C/T]TGATTAGTAAAGCAC	10529
rs150865857	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21159496	CAACTGCTACCCCAT[C/T]GACCAATTCTTTTCC	10529
rs150869754	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21091687	CTGAAGTACAGTGGC[A/G]CAATTATAGCTCACT	10529
rs150879546	snp	A/G	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:20984179	ATATTAAAAACAGGT[A/G]CACCAAAAACACATA	10529
rs150879957	snp	A/C	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21053609	CCTCATCCAATGTTC[A/C]CTTATTATAATAATC	10529
rs150885264	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20903796	TGCATGTTGTCTGTC[A/G]CTCATAAGTGGCAGC	10529
rs150897897	snp	C/T	0.0103295	0.0711199	intron-variant	NEBL	GRCh38.p7	10:20809454	ATATAATTCTTTAAA[C/T]CTACCTTTAAAAAAT	10529
rs150909263	in-del	-/AC	0.144296	0.226554	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20960710	ACACATGTATTTTAT[-/AC]ACACACACACACATA	10529
rs150946379	snp	C/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20839702	GGGTGACCATGAGAG[C/G]ATAATCAGCACATTC	10529
rs150955323	snp	A/G	0.0287284	0.116357	intron-variant	NEBL	GRCh38.p7	10:21022428	CACTTGCGAAATAAA[A/G]ATTAAATATTGTAGC	10529
rs150956488	snp	A/C	0.00517822	0.0506191	intron-variant	NEBL	GRCh38.p7	10:21090205	TTATCACCCCAAGAA[A/C]CACTGCCTACTAAAA	10529
rs150967744	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20923253	TTGTATTTCTTGTAG[A/T]GATGAGGTTTTGCCA	10529
rs150973634	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21125104	GGAACAGTCCTATGG[C/T]GGCAAAGAAGAGACA	10529
rs150979487	snp	C/T	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20964942	AACATAACCAGCCCC[C/T]GTGTCCATGTGTTGT	10529
rs150988270	snp	A/T	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:20934300	AAGCATCTCAGGAGC[A/T]GAAGGGATATATAAA	10529
rs150995065	in-del	-/GGAATTAAAA	0.00557542	0.0525036	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21127738	CTGCAACAAATAAAG[-/GGAATTAAAA]GGGGGAAAGGAGTGG	10529
rs151001552	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20782516	GTCAAGCTCAGCATG[C/G]AGAGGATAAGGAAAG	10529
rs151003899	in-del	-/C	0.0232847	0.105357	intron-variant	NEBL	GRCh38.p7	10:21001501	CTCCAGGGAAAGAAA[-/C]CCCCAAGGAACATCA	10529
rs151007067	snp	C/T	0.00557542	0.0525036	intron-variant	NEBL	GRCh38.p7	10:21027789	CATTTTACCCAATGA[C/T]CAAGACCATAACTAA	10529
rs151012132	snp	A/G	4.96233e-05	0.00498088	intron-variant, stop-gained, nc-transcript-variant	NEBL	GRCh38.p7	10:20808627	TGCTGGAATGGGATC[A/G]AGACCAGTGTCGCCT	10529
rs151024067	snp	A/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21064599	TTAAATGTATGTTGC[A/T]CCTTTATTAAGTGTT	10529
rs151028038	snp	C/T	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:20968556	AGGAGGGAGGAATCA[C/T]AGAAGTTCAAGGGGA	10529
rs151033141	snp	A/G	0.00953873	0.0683987	intron-variant	NEBL	GRCh38.p7	10:20911496	CTGAATGGCCAATAA[A/G]GTATAGGACATTTAT	10529
rs151035799	snp	C/T	0.000527913	0.0162382	intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20826478	TGATTTTTCTTCACT[C/T]GTTCGATCTCTGGGC	10529
rs151042481	snp	G/T	0.0399052	0.1355	intron-variant, downstream-variant-500B	NEBL, LOC102725112	GRCh38.p7	10:20880216	AAATACAAAAATTAG[G/T]CCGGTGTGGTGGTGG	10529
rs151045950	snp	A/G	0.0142736	0.0832652	intron-variant	NEBL	GRCh38.p7	10:20793584	TTTAACACAGGATCT[A/G]GCTCTGTCACCCAGG	10529
rs151046826	snp	A/G	0.00557542	0.0525036	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21131697	GAACACTGCTTCAAG[A/G]TTGAAACAGAAGCAG	10529
rs151063320	snp	C/T	0.00795532	0.062565	intron-variant	NEBL	GRCh38.p7	10:21170761	CACATATTAAACAGT[C/T]TTCACCAGATAAAAT	10529
rs151071772	snp	G/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21075600	CCCAAAAGTGAGAGG[G/T]TGGCCACCGGTCTGC	10529
rs151087770	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20858165	AAGGAAGCAGGTGAG[C/T]ACATGAACGCTGCAG	10529
rs151104436	snp	A/C	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20925386	GAAACAGCAAAAGTT[A/C]ATCTTTCCCCTCTTA	10529
rs151106272	snp	G/T	0.00557542	0.0525036	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20869998	ATTTGTATAGCTATA[G/T]TAACTCTTTATACTA	10529
rs151110574	snp	C/T	0.00795532	0.062565	intron-variant	NEBL	GRCh38.p7	10:21115577	GTGCTGCTCCATTGT[C/T]TTCCGACTTGCATTG	10529
rs151113543	in-del	-/GGGTTTTT			intron-variant	NEBL	GRCh38.p7	10:21071611	CTAATGCAGTGGCTG[-/GGGTTTTT]TTCTTTTTAAATGTT	10529
rs151122878	snp	G/T	0.0115144	0.0749975	intron-variant	NEBL	GRCh38.p7	10:21106754	TGATGGGGATAGTAT[G/T]GAATGTATAAATTAC	10529
rs151123662	snp	C/T	0.0279526	0.114869	intron-variant	NEBL	GRCh38.p7	10:21014170	ACTCTGTCACCCAGG[C/T]TGGAGTGCAGTAGTG	10529
rs151126796	snp	C/G	0.0107246	0.0724382	intron-variant	NEBL	GRCh38.p7	10:20946191	AGGCAGCCCTCATAG[C/G]CTGTATGAGCAAGGA	10529
rs151132572	snp	C/G	0.00716266	0.059414	intron-variant	NEBL	GRCh38.p7	10:21157010	TTCTCCTACAAGCAA[C/G]AACAATCTATCAGAG	10529
rs151158982	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20874818	GATCTCAGCTCACTG[C/T]AACCTCCACCTCCTG	10529
rs151159657	snp	A/T	0.0170251	0.090679	intron-variant	NEBL	GRCh38.p7	10:20807183	ATACAAAAATTAGCT[A/T]GGTGTGGTGGCACAC	10529
rs151168793	snp	A/C	0.0166325	0.0896639	intron-variant	NEBL	GRCh38.p7	10:21054181	AATAGTGCTGTGAGA[A/C]ATGAACTAGAAACAG	10529
rs151185013	snp	A/C	0.00755907	0.0610114	intron-variant	NEBL	GRCh38.p7	10:21094138	GAAGTGGGAGGATCA[A/C]TTGAGGTCAGGAGTT	10529
rs151187008	snp	C/G	0.0263992	0.111815	intron-variant	NEBL	GRCh38.p7	10:21001054	AGGAAACCAATGCAG[C/G]TCCCCATGAGCTTGT	10529
rs151197850	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20986833	CATACTCTCTCCAAA[C/T]AGCATCAGAATAATA	10529
rs151197900	snp	A/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20959483	AAAACTGGACTTGCC[A/G]AAGTACTACTTTTTG	10529
rs151201785	snp	A/G	0.00438332	0.0466095	intron-variant	NEBL	GRCh38.p7	10:20904842	TTGGCTGTCAACACC[A/G]TATCAAGAGCCAGAA	10529
rs151205839	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21162257	GTGTCTCTTCATCTG[A/G]CTGGTCTTGATTTGT	10529
rs151211299	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20811237	ACAATCATAATTTCA[A/G]CCTCAATGGTTTTGA	10529
rs151236878	snp	A/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21099254	AGTGACGGGTATGAA[A/T]TCAATGATTCCCATT	10529
rs151238367	snp	C/G	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:21004223	GTGTTGTTTGAAGAA[C/G]TTTCTTCTTCATGAA	10529
rs151242221	snp	C/T	0.0138799	0.0821421	intron-variant	NEBL	GRCh38.p7	10:20938298	ATGTCTGCTGTTCTG[C/T]AGCCTCCGCTGCTGA	10529
rs151247825	snp	A/C			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20861663	ACACTGTATTAGCTA[A/C]ATGGTAAAAGTAGGT	10529
rs151251928	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20907949	ATTTTATTTGTGTTA[C/T]ACCTCATCCAAGCTA	10529
rs151275892	snp	A/G	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:20797843	GGTGGTTCCATGCCT[A/G]TAATCCCAGCAACTC	10529
rs151277895	in-del	-/GTAGAAC			intron-variant	NEBL	GRCh38.p7	10:20982375	CCTATTTTTTTATTT[-/GTAGAAC]GTTGAACTTGAGCAA	10529
rs151278846	snp	C/T	0.230896	0.249269	intron-variant	NEBL	GRCh38.p7	10:21108264	ATGTTAGGGTGTCAA[C/T]ATTAGATCTTTCCTT	10529
rs151281521	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21040924	CCTCTTCACTTTCCA[C/G]CTAAGTTTCCCGAAG	10529
rs151295472	snp	C/T	0.0482946	0.147699	intron-variant	NEBL	GRCh38.p7	10:20942593	AATTGGCAAATGGGA[C/T]CTAATTAAACTAAAG	10529
rs151296753	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20887990	CTTTCAACTTTCATT[C/T]GGTATTTAACACCCA	10529
rs151313912	snp	C/G	0.00159617	0.0282053	intron-variant, utr-variant-5-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20897566	CATAAAAAGGACTTA[C/G]AGATTCTGGGAAAAC	10529
rs151317503	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20836181	GTGTCTCGGTGTCAC[A/T]TTTTGGTAATACAAT	10529
rs151321114	snp	C/T	0.00993419	0.0697739	intron-variant	NEBL	GRCh38.p7	10:21153133	GTTTATATGCATTAT[C/T]TCATGTAAACCTCTC	10529
rs151325882	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21083181	GCCTTAAAGATTCTT[C/T]AGAGAATAGAAACAC	10529
rs151326593	snp	C/T	0.0103295	0.0711199	intron-variant	NEBL	GRCh38.p7	10:20801929	AGGGCTAGGCCATCC[C/T]CATAAGACTCTCTCA	10529
rs151326720	snp	G/T	0.000798403	0.0199641	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21140597	TTTGTTCTTATTTCC[G/T]ACTCTACTTTCTAGA	10529
rs151337578	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20977316	TTTCTTCTAGTGGCA[A/G]GTCGTCTTCGTTCCC	10529
rs180675660	snp	A/G	0.00438332	0.0466095	intron-variant	NEBL	GRCh38.p7	10:21112040	CAAAACCACAATGAG[A/G]TACCATCTCACGCCA	10529
rs180676399	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21075902	CTTCAAAGAAAATAG[A/C]CAAATGACCAAGAAG	10529
rs180681109	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21098245	ACACATACGTACACA[C/T]ACTTGTACACATTCA	10529
rs180682636	snp	G/T	0.000798403	0.0199641	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21131378	AGAGGGAATACTTCC[G/T]AACTCATTCTTACGA	10529
rs180694621	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21090156	TTAGGCCAAGAGCTA[C/T]GGTCTTCCCAGTGAA	10529
rs180695607	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21150812	CTTCAGATGTTTTCC[A/T]AGGTGTCCAAATTGT	10529
rs180705423	snp	C/T	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:21122177	ATTACAGGCACCTAC[C/T]ACCATGCCTGGCTAG	10529
rs180712775	snp	C/T	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:21034833	AAGTTCCAGGGTACA[C/T]GTGCAGGATGTGCAG	10529
rs180715199	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21105888	ACCATTCTAACTGGC[A/G]TGAGATGGTACCTCA	10529
rs180715215	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21167941	ATGAAAACATGGCAC[A/G]CACTCAAGTACACCA	10529
rs180718773	snp	A/G	0.00716266	0.059414	intron-variant	NEBL	GRCh38.p7	10:20989983	ACATTGATAAAAATC[A/G]GAAATATTTTCCTGT	10529
rs180718857	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21007574	ACCCTTATCATCTGA[C/T]GGCACAATATCATCC	10529
rs180727298	snp	C/T			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21143580	TAAAAGAAAGGAGAA[C/T]ATAGACAAATATCAG	10529
rs180728923	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20974692	AATGGTTACACATAC[C/T]ACCAATTAGATGCTC	10529
rs180745400	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21082267	TGGATCCTTTTGCAA[C/T]AAAGAATATTTATTT	10529
rs180747599	snp	G/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21067263	GGTGTGAGCCACCGC[G/T]CCCAGCCGAAATAAT	10529
rs180747671	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21028053	CCAATGTGGTGAAAC[A/C]CTGTCTCTACTAAAA	10529
rs180751425	snp	A/T	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:21016450	GAAGAGAGGGGGGGA[A/T]ATAAAAAGAAAAGAG	10529
rs180755391	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21042072	ACTGTATCTTGTGCC[A/G]ACCTCCTATCTCATC	10529
rs180762927	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21060713	TTCTCTAACTCCTCT[C/G]TTTCCATTCTCTCTT	10529
rs180783780	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20877280	TTTACAGATGAGAAA[A/G]TGGAGATTTAGAGAC	10529
rs180785299	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20890015	ATGGCCTTTTTTGAA[G/T]GATAATTAGGTTGAT	10529
rs180791531	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20852758	AAGAGCTGCAAAGCT[A/G]TTGCCAAGTCCCCAT	10529
rs180793344	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20904445	TTAAAAAATTCTTTA[A/G]TGATGCAAGTGATTT	10529
rs180796510	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20803978	TATTTTATAAAAATA[A/G]TTATACTTATATATA	10529
rs180801266	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20790543	GAGGAGGAGGTTGCA[A/G]TGAACCGAGATCATG	10529
rs180802729	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20827147	TTTATGAGTGCCCTC[A/G]TTATGAGTACTCTGC	10529
rs180809306	snp	A/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20835412	AACTGTTAAACCAGC[A/T]GCAATGCTTTGAGAA	10529
rs180809583	snp	A/G/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20819564	ATGGGAAATAAATAC[A/G/T]TCCCAAAACATTGCA	10529
rs180819044	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20857776	GACAAGACTAAAAGC[A/G]ATGTGTCAATGCAGT	10529
rs180819164	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20842549	AAAAGTCCTCTTTTT[C/G]AAATTAGACAAGCTA	10529
rs180834654	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20796460	AACACACAACATTAG[C/T]TGTATTTTTAATTTT	10529
rs180850975	snp	A/G	0.000214849	0.0103624	intron-variant, synonymous-codon, nc-transcript-variant	NEBL	GRCh38.p7	10:20809870	AAGGTCGAAGATGGA[A/G]CCAGGATCTGTGCGC	10529
rs180860486	snp	A/G			downstream-variant-500B	NEBL	GRCh38.p7	10:20779856	GAAAAAAGGTAGTGA[A/G]TTCTTCAAATAAATA	10529
rs180879544	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20830102	TCAGGATCATCCCAG[C/T]GGCTGTGTCGGCTGC	10529
rs180887400	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21108856	CTGTATTGGGTGCAT[A/G]TATATTTAGGATAAT	10529
rs180898865	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20799672	CAGAAGTCAGGCTAG[A/C]AAGGAGTTGGATTGG	10529
rs180899158	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20793627	GATGCCATCTCAGCT[C/T]ACCGCAGCCTCCATC	10529
rs180902398	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20814755	GTGTTAAAAAATGCA[C/T]ACAAGCTACTCTATT	10529
rs180911754	snp	C/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20846612	ACAACGACTAGAAAC[C/T]TTCCTCTTCCTTATG	10529
rs180914175	snp	C/G	0.0107246	0.0724382	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21126958	CCAGCCTGGGTGACA[C/G]AGGGAGACCCTGTAT	10529
rs180947866	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	C10orf113, NEBL	GRCh38.p7	10:21147981	TCCAGAAAAAATAAC[A/G]GAACTCTTCGTTATC	10529
rs180956279	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20784040	AACTTTTCTAAAGTG[A/G]AAATAAATTAGCTTT	10529
rs180959837	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20955157	AAATTAGAGAGGTGA[C/T]GAGAAATGCAAAGTA	10529
rs180968066	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20945485	AGAAAAAGCATCAAC[C/T]CTTAATAACATCATG	10529
rs180988975	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21163500	TTCACACTCTGGATC[A/T]ATTAATGGATACAGA	10529
rs181006051	snp	A/G	0.00874735	0.0655527	intron-variant	NEBL	GRCh38.p7	10:20917481	GTTGAGACTGTTCAG[A/G]GGATGTCTATTTATT	10529
rs181006589	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20931944	TACTAACAGCATATT[C/G]TTTCATGTATTCCTT	10529
rs181007757	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20873039	TGTGAGATCCAAGAA[C/T]GTCTTTTGGGGTCTG	10529
rs181010502	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20981971	AACAAAAAGAATTCC[C/T]AACTGATACACTCAT	10529
rs181026408	snp	A/G	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20998177	TGACAATGCTGAGAT[A/G]GCTAATAAGAAACAT	10529
rs181047673	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20861289	TTCACGCCATTCTCC[A/T]GCCTCAGCCTCCCAA	10529
rs181049769	snp	A/G	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:20901911	TGAAAGAAGAAATGT[A/G]AGCACTCTAGGACAA	10529
rs181060508	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20839575	CTAAAGTGCCTTTTA[A/G]ATGTTTCCTTTATTT	10529
rs181060789	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20822854	CATATTGCATAGTGG[C/T]GATGTCTGGGCTTTT	10529
rs181076148	snp	G/T	0.00398564	0.0444627	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20854686	CTTCCCATCTTAGCC[G/T]CCCAAGTAGCTGGGG	10529
rs181082041	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:20905441	CATGGTGGCAGGCAA[G/T]AGAGAGCCAGCAAGA	10529
rs181088886	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20919560	AGAGATAGACCCATG[C/T]CCACAGGACAAACGT	10529
rs181093806	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20803051	CCAGTTCAGGGTTCC[A/G]GCCACCGCAGGACAC	10529
rs181104949	snp	A/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21031190	ATGTCACTAGGGTGG[A/T]GGCAGAGAGATAGGA	10529
rs181109949	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21044634	CACTGAGATTTCCAA[A/G]CAAATCCATTTGCTT	10529
rs181110241	snp	A/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20934041	TTAATGTTGAAATTT[A/T]AAAAAAAAGGCCCCA	10529
rs181112819	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20897642	CTCAAAGATTCCTTG[C/T]CTCTGTCTAAATAAA	10529
rs181115245	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20858528	AAAGTTATTTCTATA[C/T]GGGCTTGAGAATACT	10529
rs181123017	snp	C/T	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:20890721	CTTCCCCTTTGGGGA[C/T]AGGCCAGAATTGTTA	10529
rs181124168	snp	A/C	0.00597247	0.0543191	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20877486	AAGCAGCCCCGAAGT[A/C]TTTTTCTTTTCTAAC	10529
rs181141524	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20827295	CTCCAAAGGCTAGAA[C/T]TACAGAACACTATAG	10529
rs181146261	snp	A/G	0.0138799	0.0821421	intron-variant	NEBL	GRCh38.p7	10:21064005	TGAGCCCGGGAGGCA[A/G]AGGTTGCAATGAACT	10529
rs181150289	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21080244	CATCACTTTCTAAAT[A/G]GATACTTTGGATATG	10529
rs181150650	snp	C/G	0.00636936	0.0560724	intron-variant	NEBL	GRCh38.p7	10:20810476	TAAGTGTATCTTAGG[C/G]AATGCATATCTTATT	10529
rs181154511	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20843072	GCCCCCATTGTGACC[A/G]TACTTGAAGGTGGGA	10529
rs181183494	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20796809	ATAAGCAGGATTGTC[A/G]GTGAGGGAAAAGAAA	10529
rs181186058	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20780479	ATATCTTGACTGATT[A/C]ACCAATGTAAATGCA	10529
rs181204964	snp	A/G	0.00953873	0.0683987	intron-variant	NEBL	GRCh38.p7	10:21053985	TTGCAGTGAGCCAAG[A/G]TCACACCACTGCACT	10529
rs181217822	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21013466	GGCGTTCAAAGAAAA[C/G]AGAAAGTTAGGAGGC	10529
rs181217955	snp	A/G	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:20985131	TAATAGACATAAAGT[A/G]TACAATAAATGTAAT	10529
rs181222509	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21085239	GTAGAATGCCCTTCT[A/G]AGATTTTACTAAGTC	10529
rs181223831	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21071144	CCACTGCACTCCAGC[A/C]TGGGTGACAGTGACA	10529
rs181227647	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20969445	TTCACAATCCAACTT[G/T]ACCAGATTTGGGGTT	10529
rs181233799	snp	C/G	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:21102983	CTCCCTCCCCCCACC[C/G]CACTTCCAGACAGGC	10529
rs181242365	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20927249	CAGATGCCCACAGAA[C/T]ATCATAGCCGACTAT	10529
rs181252033	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20949846	CTGGAATACTGATAG[A/G]CAAATAGTGAATAAA	10529
rs181256337	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20994132	CGTAATTTAAACTGT[C/T]TTTCAGTTCAGCCAG	10529
rs181257822	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21020919	TTGGGGCCTCTCTGT[A/G]AGCTGACTACTCCGA	10529
rs181264056	snp	A/C	0.00478085	0.0486577	intron-variant	NEBL	GRCh38.p7	10:20942414	AAACTGGATCCCTTC[A/C]TTACACCTTATACAA	10529
rs181277374	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20959611	AATAATAAATTCACC[A/G]GACCTCAGAGCACTT	10529
rs181279046	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21001415	GATTTTTCCAACTTG[C/T]AAGGTGGACATCATT	10529
rs181280346	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20982338	ACACAAATTTTAAAA[A/G]GTCTCAATTTCAGCA	10529
rs181283149	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21151242	TGTAATTCACCCTGC[C/T]TCAGTCAACAGTCAT	10529
rs181283753	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21005705	TGCCACTGCACTTCA[A/G]CCTGGGTGACAGAGC	10529
rs181284274	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21168770	TGGCTCAACAGTGGC[C/T]GGGCGCGGTGGCTCA	10529
rs181284412	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21025994	CAAAGTAATTTAACC[C/T]CTGTGTCTCACGACC	10529
rs181292039	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:20964376	TTTATTTGGCTTATG[G/T]TTCTGTAAGCTGTAC	10529
rs181294708	snp	C/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20789840	GTGACAGAGAGCAAT[C/G]TTATCTCAAATTTTA	10529
rs181296823	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20945617	GAGAAGAAAGTCTGG[A/T]TCCCAGTGTTAAGAA	10529
rs181296844	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20988437	TTTCCCACCAAAAAA[A/T]AATTGACCAACCCTC	10529
rs181299853	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21059268	CAACCCAGGCACTCC[A/G]TATGGTCTGCACCAC	10529
rs181303810	snp	C/T	0.0364509	0.129988	intron-variant	NEBL	GRCh38.p7	10:21035173	TGGCTAATTTTTGTA[C/T]TTTTAGCTGAGACAG	10529
rs181309314	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21041053	ATGTAAAGAACTAAC[A/G]CACTTTCCAACTTTT	10529
rs181315425	snp	A/G	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20914538	TTGTTTAATAATATT[A/G]TTCAATGCTTTCCTT	10529
rs181321342	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20902675	TGAGCTGAAAGTCTT[C/T]GGTTTCATTTACAGC	10529
rs181327359	snp	C/T	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:20917533	CGAACTATTCACATG[C/T]TGGCCACACATTACT	10529
rs181334535	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20979255	AGACCTTGTCTCTAC[A/T]ATAATAATAATGATA	10529
rs181336269	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21037420	ATCAAGTTAGATCAA[G/T]AAAGTAAGAACAAAT	10529
rs181341356	snp	A/T	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:20932597	AAGTAAAATTTTTTT[A/T]AAATTTTTAAGAAAA	10529
rs181343419	snp	G/T	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:20974005	CAAAATTCTCATTTT[G/T]TTCAAGTTAATGAGC	10529
rs181346635	snp	C/G/T	0.00557542	0.0525036	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20854999	GGAGGCAGAGACAGG[C/G/T]GGATCATGAGGTCAA	10529
rs181349814	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20888798	CCAATATTTTGCTCT[A/G]CAATTAACTCCTTCA	10529
rs181351808	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20908516	GGATCCTTGATCTAG[C/T]AGGAACCTAATTTGA	10529
rs181357587	snp	C/T	0.00119737	0.0244387	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21131872	TTGGTAAAAGTTTCC[C/T]GCTGTTGTATTTTTT	10529
rs181358497	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20938737	CCAATGCAAAGAAGT[A/C]CTCAAAGGACCTGAT	10529
rs181397661	snp	C/T	0.00199481	0.0315187	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21127530	AGATATACTGGAAAG[C/T]ACATAGCACCAACTA	10529
rs181398274	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21016854	TTAGGATAGATACCT[A/T]CCCACGTTTTTGCAA	10529
rs181402807	snp	A/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21109218	CATGAAGGGCTGTTG[A/T]ATTTTATCAAAGGCC	10529
rs181414557	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21159119	TTTCCTCCACCCTTT[C/T]TTTAAAGATGTATTC	10529
rs181424760	snp	G/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21067787	TTCAAGACCAGCCTG[G/T]GCAACATAATGAGAA	10529
rs181426673	snp	A/C	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20922231	GCTGAGAATTAAATG[A/C]TTCTGTGCCTCACTG	10529
rs181441069	snp	G/T	0.00517822	0.0506191	intron-variant	NEBL	GRCh38.p7	10:21085322	ATTTTCAGTTAATTT[G/T]TTTTAAAACAGCACG	10529
rs181450398	snp	A/C	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21098865	CAGGCATGGCGGCTC[A/C]CACCTGTAATCTCAT	10529
rs181458337	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20848091	ACCTTTCTCTGGGCT[A/G]TGGGTCAGTGACAAT	10529
rs181460285	snp	C/T	0.0023933	0.0345097	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20862344	CACAAGTTTCCCTCA[C/T]TAATGAACCACAATA	10529
rs181467397	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20894060	TGTACCACTCTGCAC[A/G]GTTCTGATTATTACA	10529
rs181477063	snp	C/T	0.000798403	0.0199641	intron-variant, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20873608	TATTATGTACCATAT[C/T]AAGGACTTAACATTC	10529
rs181479963	snp	A/G	0.00795532	0.062565	intron-variant	NEBL	GRCh38.p7	10:20814974	GTATGCTAAGAAAAG[A/G]GCCTGTGTTCTTCAC	10529
rs181481900	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20953579	TATGATATATTAAGA[C/T]AGGGGAAGTCCTGGC	10529
rs181489880	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21103252	GAGTCTCACTCTGTT[A/G]CCCAGGCTGGAGTGC	10529
rs181491072	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21022553	TCCAGGTAATTGGAG[A/T]TAACCCCATAACTGC	10529
rs181494308	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20830673	GTTAAAAGACAAAAC[A/G]TTTGTAATTTATTTT	10529
rs181499197	snp	A/G	0.00318978	0.0398085	upstream-variant-2KB, intron-variant	C10orf113, NEBL	GRCh38.p7	10:21148351	GTATCTCTTCTGTTA[A/G]AGTATGTGGACTTTG	10529
rs181499619	snp	A/G	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:21002534	TCACGCTGCTATAAA[A/G]AACTGAGACGGGGTA	10529
rs181501083	snp	C/T	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:20985242	AAGGTTGGTGACCGC[C/T]ATGGTGAAGAAAATG	10529
rs181501609	snp	A/G	0.00159617	0.0282053	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21138624	TTTTAAAAAAACTAT[A/G]CTCCAGGTGCTATGT	10529
rs181502468	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20784255	CAGGTCACAGTAAAC[A/G]GCACAATCAGAAAAA	10529
rs181515113	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20799865	TGATGGTATGGGATA[C/T]ATATACGTGGTAAAA	10529
rs181515575	snp	A/G	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:21071553	TTACAATCACCTAGG[A/G]CACTTTTAAAAATAT	10529
rs181517043	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21038023	TAGATTCTTCAGAAA[A/C]CTTCTAGAGAGAGAG	10529
rs181535059	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21165093	AGTAAAAGAGTGGAC[A/T]GACATTTGGGTCCTG	10529
rs181570829	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21082643	TAATTCCGATGCCCA[C/T]TTTGATCCTATACCA	10529
rs181572051	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21049998	GAACATGAAAGGTTA[A/C]TGAAGAGCATAGGAT	10529
rs181599636	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21112463	ATGAAGCTGGAAGTG[A/G]TCATTCTAAGCAAAC	10529
rs181616420	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21117609	CTGTCTGTGCTGCTT[C/G]CCTAATGTCTGACAA	10529
rs181618168	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20958600	AATATATTCAATGAG[A/T]TGAAGACATCTTCTG	10529
rs181631026	snp	A/C	0.00716266	0.059414	intron-variant	NEBL	GRCh38.p7	10:20941324	CATAAACAGAACCAA[A/C]GACAAAAACCACATG	10529
rs181636848	snp	A/G	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:21153521	TATATTAAAACAAAT[A/G]TATATATTATATATG	10529
rs181638713	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20926149	AAAATGGCTTGAGTC[A/G]CTACTGGCATCTTTT	10529
rs181648614	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20880029	CTGTCATATTCCCCA[C/T]GGGTCTTAGGTTGGA	10529
rs181649380	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21083317	GAAACTGTGTAGTTG[C/T]TGTATTTGACTATCC	10529
rs181650402	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21121632	ATCTTAGAATGAGTC[A/G]TAGAGAGCAAATCCA	10529
rs181655782	snp	A/G	0.00199481	0.0315187	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21143357	GGGAGGCTGAGGCAG[A/G]AGAATAGCTTGAACC	10529
rs181657007	snp	G/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21157526	CAGTGAGCCGAGATG[G/T]TGCTACTGTACTCTA	10529
rs181663756	snp	C/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20884118	TAGTCATATACACTT[C/T]GTTTATATAAGTGAT	10529
rs181676822	snp	A/C/G	1.64827e-05	0.00287073	intron-variant	NEBL	GRCh38.p7	10:20897090	GTCAATTTAGAGGAA[A/C/G]AAACGCTGGTCTGAG	10529
rs181680280	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20913523	AAGAGGTTTTAAACA[A/T]CTTTGATATATTGTC	10529
rs181687672	snp	G/T	0.00238245	0.0344318	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20852517	GTTGCTGGCAGGGAG[G/T]GTAGGTACCGTACGG	10529
rs181689145	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20812112	GAGTACCATCAGAAC[A/G]CCCATGGCGTGTCTG	10529
rs181711318	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20867701	GAATTCATTTTTGTA[C/T]ATGGTTTAAGATTTG	10529
rs181714123	snp	G/T	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:20843416	GCATGTATTCTGAAT[G/T]AATAAATTAAGACTC	10529
rs181714334	snp	A/G	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:20827784	GCAGGGACATGGATG[A/G]AGCTAGATGCCATTA	10529
rs181725154	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20803246	TACAGTTTCAAATAG[C/T]TAGAAGGATGTTTAA	10529
rs181727435	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20894264	CACTTAAAGCCAAGA[C/G]CTTGAGACCAGCCTG	10529
rs181733735	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20909632	AATGCTAATTGAAAA[C/T]AGTATTATAGTAGTG	10529
rs181737212	snp	A/C	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:20834822	GTTCAAGAGGTGTAG[A/C]GAAAGTTCTAGGGTA	10529
rs181739872	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20922767	AGCACTCGAGCCATC[A/C]CATCCCTTCCGTTGC	10529
rs181745861	snp	C/T	0.00636936	0.0560724	intron-variant	NEBL	GRCh38.p7	10:20945266	TAAGCCATCTGGGAC[C/T]GTCACCAAACCCCAG	10529
rs181748956	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20848582	TCCTGTCAGATCAGC[A/G]GTGGCATTAGATTCT	10529
rs181755349	snp	G/T	0.000798403	0.0199641	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20863940	GGAGGAGGGAGTGCT[G/T]GCCAGGATGGGAGAA	10529
rs181758933	snp	A/G	0.00159617	0.0282053	intron-variant, downstream-variant-500B	NEBL, LOC102725112	GRCh38.p7	10:20880347	CCTGGGTGACAGAGC[A/G]AGGCTCTGTGTCAAA	10529
rs181789906	snp	A/G	0.00716266	0.059414	intron-variant	NEBL	GRCh38.p7	10:21113436	CATCAATTATGTGAA[A/G]AGTTGCTTCTGGATG	10529
rs181802273	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21151716	CACACGCCCCAGGTT[A/C]ACTCCGTGCCCTTGC	10529
rs181831171	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20792759	GAGCTGAGATCGTGC[A/C]TTTTCACTCCAGCCT	10529
rs181836472	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20822303	TTCATGTTTAGTTTT[A/G]TCACTTGTTTTGTTT	10529
rs181840241	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20806347	ACTGACCTCGGGTGC[A/G]GCCTCCTCTTCTAAA	10529
rs181850749	snp	C/T	0.0197687	0.0974348	intron-variant	NEBL	GRCh38.p7	10:20938896	TTAGAGAAAAAAGAA[C/T]AAAAAGAAATGAACA	10529
rs181853036	snp	A/G	0.00636936	0.0560724	intron-variant	NEBL	GRCh38.p7	10:20890940	GTTTATCCTCCCAAG[A/G]CCATAAATACTTAAA	10529
rs181858355	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21011926	TGCCATCGCCTTCCA[C/T]ACTATGGGAGAGACT	10529
rs181859506	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20950409	TGGGATCTCTCCCTG[A/C]ACTCTAACAAGGAGA	10529
rs181862674	snp	C/T	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:20919982	GAGAAAAAAAATCAA[C/T]AACCCAATATGGACA	10529
rs181867692	snp	C/T	0.00636936	0.0560724	intron-variant	NEBL	GRCh38.p7	10:20978323	TAAATGAAGACAGAT[C/T]AATAATATCCCGAAG	10529
rs181871570	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21089976	CGTACAAATGGCCTC[C/T]ATGTTGATGACTCCC	10529
rs181874280	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21068096	GTGAATTTCTCTACT[A/G]GGTGGGAAAAAAGGC	10529
rs181880125	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21105781	TTTTCCACAATGGTT[C/G]AACTAATTTATACTC	10529
rs181880208	snp	C/T	0.00716266	0.059414	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20858832	CACTTTTCTAAATTC[C/T]TTTATATGTATTAAG	10529
rs181887831	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20993488	AATAATAGGCATTCA[C/T]GCGTCTTGCTCATGA	10529
rs181888855	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21050205	GGACATCATTAGATA[C/T]GTGCTGATAAATTCT	10529
rs181890999	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20979146	CGTAGGACTGGGCAC[A/G]GTGGCTCACGCCTGT	10529
rs181899078	snp	G/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21044374	CGCACTCCAGCCTGG[G/T]TGACTGGGTGACAGA	10529
rs181906430	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21012406	ACTCTGTCACCCAGG[C/T]TGGAGTGCAGTGGCA	10529
rs181938557	snp	C/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	NEBL	GRCh38.p7	10:20818850	CTTCAACAAGGAAAT[C/G]TGAAAAGGAACATCC	10529
rs181945502	snp	A/G	0.00119737	0.0244387	intron-variant, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	NEBL	GRCh38.p7	10:20958856	CTCACCTCGTTCATC[A/G]CACTCAATTTGAAAT	10529
rs181947937	snp	A/C	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20942194	CTTCAAACTATACTA[A/C]AAGGCTACAGTAACC	10529
rs181949951	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20930834	ATACCATAAGGTTTG[A/C]CTAGAATGATGCTAA	10529
rs181951359	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20901409	CACCTTCCTTGAGGT[C/T]GCCTATGACAAGACT	10529
rs181958911	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20838368	GTGGAAATAGCAAGA[G/T]AACTAGAATTAGAAG	10529
rs181973263	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20872572	TCCATCTTGAGAAGG[A/G]AATGGGTAAAATGAG	10529
rs181975081	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20816272	CTGTAATAAATATTT[A/G]ACCACAAAAGGAAAT	10529
rs181983299	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20785997	CAATCACAACACACC[A/G]ACCCACACATAAAGT	10529
rs182001361	snp	C/T	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21139213	GTCAAGCTCTAAAGC[C/T]TATAATTCAAAGTAA	10529
rs182002788	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21117849	TGGGTTCAAGTAGCA[A/G]CTCGGCCGCTATTAT	10529
rs182010859	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20790463	AAAAATTAGCTGGGC[A/G]TGGGGTGTGTGCCTG	10529
rs182014138	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21026480	TAAACTTTGTTTTCA[C/T]TCCTGTCTCCTGGTG	10529
rs182019031	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21154653	GCTAAAGAGATGCTG[G/T]ATGTGCACTTTCCTC	10529
rs182027908	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21100237	AGCGTGTGTGGGATG[C/T]GTGGTACCCGACCAT	10529
rs182053826	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20954947	CAGCTAGCACTAAGC[C/G]AGGGACAGCCTCACA	10529
rs182065109	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21085486	AACAAAAAAACTTAA[A/T]TAGCCAAGCATAGTG	10529
rs182065910	snp	A/G	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21133374	AGGGGGCTCCTTACT[A/G]TGGGTGAAATGTGAC	10529
rs182075194	snp	A/C/G	0.00914918	0.0670815	intron-variant	NEBL	GRCh38.p7	10:21170386	GCCTGATGGAAACAG[A/C/G]CTGCCCACTGAAACA	10529
rs182080741	snp	C/T	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:21072107	ACAGGTATGAGCCAC[C/T]GTGCCTGGCCCATTG	10529
rs182089361	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21103395	ATTTTTTGTATTTCT[C/T]GTAGAGATGGGGTTT	10529
rs182096860	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20988958	ACACATTAGGTACTC[A/G]ATACATATTTGCTGA	10529
rs182111571	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21061780	GTGGATAAGGACTGA[A/G]CCACCTAAATAATAT	10529
rs182114659	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20905845	GGGAGAGCTACATGA[C/T]GGAAATGTATAGAAA	10529
rs182116851	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21083674	ACATGGCAAAATCCC[A/G]TCTCTACTAAAAATA	10529
rs182118005	snp	C/T	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20970459	GCCTGGGCAACACAG[C/T]GAGACCTTGTCTCTG	10529
rs182124589	snp	G/T	0.0256215	0.110247	intron-variant	NEBL	GRCh38.p7	10:20992905	ACCTCAGCCTCCCCA[G/T]TAGCTGGGACTACAG	10529
rs182127635	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21043326	GCCGTCAACATTGAC[A/G]AATTTAGAAGCAGCC	10529
rs182127748	snp	C/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21114043	TTCTAATATAATACA[C/T]TTTTAATGCTATTAA	10529
rs182128887	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20828469	ACAATGAGGAAAAAA[C/G]ACCATTTCTTACAAA	10529
rs182129854	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21100552	GGCTGACCTCTGTGC[A/C]ATCAACAGAAAAATG	10529
rs182131357	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20934513	ATGGATGGACGTGAC[A/G]TGCATGACTTCCAGA	10529
rs182135332	snp	A/C	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20791652	ATCTTGTCTCAGACT[A/C]CCAAAGCACTGGGAT	10529
rs182146463	snp	A/T	0.000798403	0.0199641	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20877831	AAGCCTGTCTATAAA[A/T]TCCGATGCACTCTGC	10529
rs182153378	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21002596	CAGTTCTGCAGGCTG[C/T]ACAGGAAGCATGGAT	10529
rs182195794	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20916384	GCTCTGAAGAAGAAG[A/C]AAAAGACTTAATTTT	10529
rs182198880	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20884492	CAAGGAGGTCAAGTA[C/T]GCAAATTAAAATAAT	10529
rs182218036	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20913892	CTGGAGTTTTCTTTT[A/T]CAGGCTGTTAGCCTT	10529
rs182219800	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21163210	TAGAAACCCAGTTTT[C/T]TTTCCTATAAGCAAT	10529
rs182226167	snp	C/T	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:20887751	CTTTTAACAAGCTAT[C/T]CAAATATTCTCTACT	10529
rs182252305	snp	C/T	0.000798403	0.0199641	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21134858	AGGTACGCTACTCTG[C/T]AATGCTGCCGTGCTT	10529
rs182257417	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20830999	TAGCTCTCCATAATG[C/T]CTGTTGCATTGAATC	10529
rs182261108	snp	G/T	0.00159617	0.0282053	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20854399	CTGCCACAAGAGAGC[G/T]ACCCTTTCTAGTGGG	10529
rs182264910	snp	C/G	0.00597247	0.0543191	intron-variant	NEBL	GRCh38.p7	10:21151969	GGCAGGAATTTTCCT[C/G]TACTTTGCTCACTGC	10529
rs182279260	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21170638	GTTTGGGGAATATCT[A/G]TGGACTTCCCCTCTC	10529
rs182284613	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20889483	AAATGATATTCAATC[A/G]TTTATCTCTGATATA	10529
rs182289156	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20903469	TGAAGCTTTTTTAAA[A/G]AACTAAAAGTAGAGC	10529
rs182297344	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20918156	TTGAGGTCAGGAGTT[A/G]AAGACCAGCCTGGCC	10529
rs182303054	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21063103	GCATGGGGATGCCTG[A/C]AACATAACTGCGGGT	10529
rs182304703	snp	A/G	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:21094330	ATACGGTGAAACCCC[A/G]TCTCTACTAAAAATA	10529
rs182307157	snp	C/G	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:21041457	AAGGGAAGATGCAGA[C/G]AACATGGAAAAAAGC	10529
rs182307371	snp	C/T	1.90725e-05	0.00308802	intron-variant	NEBL	GRCh38.p7	10:20840714	AAAAACATATTCATC[C/T]AAGGTGTTAAATAAA	10529
rs182307938	snp	A/G	0.00398564	0.0444627	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21128920	CTAAGTAAGAGCCGA[A/G]TATCATATAAGCCAC	10529
rs182308975	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20855894	AGAATATCTCTTATT[A/G]AGCAATCTTATTCAA	10529
rs182309328	snp	A/C	0.0310518	0.120672	intron-variant	NEBL	GRCh38.p7	10:20939625	AAATGCTCCAATTAA[A/C]AGGCACAGACTGGCA	10529
rs182311040	snp	C/T	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:21038586	ATGGTGCATATGTGC[C/T]ACATTTTCTTTATCC	10529
rs182311820	snp	C/G			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20875215	CTCCTTATAATCCTC[C/G]CACTTCTGTTTCATA	10529
rs182313087	snp	G/T	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:21149308	CTTTTTTTTTCTTTT[G/T]GAGACAGAGTCTGTC	10529
rs182318513	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20922989	CCTGGTAGAATGTTT[C/G]TTAAATGAATATAAA	10529
rs182319267	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21074730	TGATCCGCCTGCCTC[A/G]GCCTCCCAAAGTGCT	10529
rs182321216	snp	C/T	0.00159617	0.0282053	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21125688	AGAAATAAAAGCACA[C/T]TCCTTCCTCCCTGCA	10529
rs182341498	snp	A/C	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20824640	AGCAGGAGTTTATGG[A/C]CCAACCTCATGCAGA	10529
rs182345728	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21050731	TGGGTGGGAGAACAA[G/T]AGTAGAAGAAAAGCT	10529
rs182346193	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21065583	ACTGTGCTAAAACAC[A/T]TTAATGTCTTAACTC	10529
rs182367310	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21081106	GTGATCCACCCACCT[C/T]GACCTCCCAAAGTGC	10529
rs182373116	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21006645	GCAGGCTACCATAAC[G/T]TTTCCAAAGGAGGAG	10529
rs182376338	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21110532	CTTTGTTCCCTATCT[A/T]TTTTTCTTAATCATT	10529
rs182376763	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21154856	TGTATAGTAGGTGTA[C/T]ATACTTGTGGGGCAC	10529
rs182380497	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21095798	GAAAATGACAAGGAA[G/T]ACTTGGGGTTATCTC	10529
rs182388484	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21077326	ATTGCTTTTGCTGGC[C/T]GGGCGCAGTGGCTCA	10529
rs182394525	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20974540	AAGCATGAGCCACTG[C/T]ACCCAGCCTTGAAAT	10529
rs182425659	snp	A/G	0.00636936	0.0560724	intron-variant	NEBL	GRCh38.p7	10:21023014	CAATAGACAGAGGAA[A/G]TTAGGCAGACAACTC	10529
rs182436753	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20948246	GAAGCAATGTAAATA[A/T]TCTTAACCATCTGTC	10529
rs182451136	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21017396	GCTTCTAAAGAACAC[A/G]ACATTTGAGCAAAAT	10529
rs182453575	snp	A/G	0.0130921	0.0798413	intron-variant	NEBL	GRCh38.p7	10:21003951	AACAAACCAAAAGTC[A/G]TCCAAAAAATCAAGA	10529
rs182457991	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20985788	AGTGAAAGCTATAAC[A/G]AAAATTATGTTTTTA	10529
rs182463025	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20971428	AGCTTAATTCACACA[C/T]AGAATAGAATTTTTT	10529
rs182467642	snp	A/C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20983263	TGCCTGGAAAATTAA[A/C/T]CATGAAAGATAGAAC	10529
rs182468034	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20801369	AACCAGCTAATTTTT[A/G]TATTTTTAGTAGAGA	10529
rs182475221	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21023411	TTAATTTAAAATTCT[A/G]GGCCAGGCACAGTGG	10529
rs182476882	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20897434	AGTGGAAATAACATA[C/T]TCTTAAGCAAAATTT	10529
rs182479041	snp	A/G	0.00636936	0.0560724	intron-variant	NEBL	GRCh38.p7	10:20786794	TCTTCAAGATTTCCA[A/G]TGGGGGATTTGAAGA	10529
rs182481330	snp	A/T	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:20926960	AAGAGATCACAGATG[A/T]GTGGGGAGGAAAAAT	10529
rs182484781	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20798646	TCTTCCCGAAAAGCT[C/T]TCTCATTTGACACAC	10529
rs182485300	snp	C/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20920438	AAATTGTAGTCCAGC[C/G]ACACACTGGAGCTGT	10529
rs182496655	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20869583	ACCCAAATAATTAAC[A/G]TAATAAAATAGATAA	10529
rs182500098	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20884835	AATGAGAAGGATCTC[A/G]CCACCTCATGGCATG	10529
rs182509383	snp	C/G	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:20952047	TAATTCAACCAAGAT[C/G]TGGAAAACTTAAAAA	10529
rs182518263	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20937501	GCTCCAGTCTACAGC[G/T]CCCAGTGTGAGTGAC	10529
rs182519730	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20836133	TCAAGCAAGCCTATC[A/G]GTGCTATTTTTCCAA	10529
rs182526625	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20819919	TAAGTCACACTTTTT[A/G]TTGTTTTCCTTCAGA	10529
rs182538673	snp	G/T	0.00119737	0.0244387	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20852964	GGACATGCGGAAAAA[G/T]GTAAAGTGGGGAAAA	10529
rs182540285	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21171077	GCGGTGGCTCACGCC[A/G]GTAATTCCAGCACCT	10529
rs182543262	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21106909	TCCTTCACATCCCTT[A/G]TAAGTTAAATTCCTC	10529
rs182543522	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20790992	ATCAGATACCATTAG[C/T]ATTGCTACAAATGGG	10529
rs182548900	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21078933	ACTGATCCAACCTTA[A/T]TAAGCACGTGCGGCT	10529
rs182554460	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21055945	TGCCCTGAGGCTACA[C/T]GGGCAAATGCTTTGT	10529
rs182555346	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20948957	CTCTGTCCTCAAACA[C/G]ATATGTGCACTCTAC	10529
rs182557346	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20804407	GGATCATTTGCTTTA[C/T]CAACCCTCATCACTA	10529
rs182558105	snp	C/T	0.00478085	0.0486577	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21146105	TTCATTTGAGTCTTC[C/T]TTTACAAATCTCCAA	10529
rs182562266	snp	C/T	0.00478085	0.0486577	intron-variant	NEBL	GRCh38.p7	10:20933590	AATACAAAAATTAGC[C/T]GGGTGTGGTGGCACG	10529
rs182585291	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21108407	TTTATTTCTGCCTTC[A/G]TTTCATTATTTACCC	10529
rs182600577	snp	C/T	0.00159617	0.0282053	upstream-variant-2KB, intron-variant	C10orf113, NEBL	GRCh38.p7	10:21147453	GCCTCCCTTCACTGG[C/T]TTTCCCTTCTCACTT	10529
rs182619355	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21035767	TTTCTTCTCAAATGG[C/T]AAACCTCCCACCCAA	10529
rs182630001	snp	C/T	0.00953873	0.0683987	intron-variant	NEBL	GRCh38.p7	10:21106230	GCTTTTGTTGCCATG[C/T]TTTTGGTGTTTTAGT	10529
rs182633329	snp	A/C	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:21033348	GTATCATACCTATAG[A/C]AAATGTGCAATATGA	10529
rs182640056	snp	A/G	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:21122722	CAGTGTCTGGGTAGC[A/G]GATCCAGAAGAGATA	10529
rs182642261	snp	A/G	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:21085872	CTCGGCAGGGCAGGC[A/G]AGTCTCTCAGATATC	10529
rs182645082	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21119387	TATACATACACAAAC[A/G]TGTATATGTGCAGGT	10529
rs182657805	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:20966457	TAACATGTGAAAATA[C/G]CAAGCAAGGATATGA	10529
rs182665084	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21000010	TTTACTACAAAGCAC[A/T]TCCTCCTCTGATGGA	10529
rs182673739	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21042366	GCTCACACTGGCTCA[C/T]GGGAGCTGACTGTGC	10529
rs182681821	snp	A/C	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20983560	TATCAAATTGCAAAT[A/C]GTTGTACCCAAAATA	10529
rs182681845	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21008889	ATTGTATGTAATGTA[C/T]GTATATTATATGTAT	10529
rs182682287	snp	C/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20933361	TTTTCAGAAAATAGC[C/T]TCAAAACTTACCCGT	10529
rs182684818	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20967430	GTCAGGAGTTTGAGA[A/C]CAGCCTGGCCAACAT	10529
rs182694318	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20999550	GCTGCAGTGAGCTGT[A/G]ATTGCATCAATGCAC	10529
rs182703194	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21061274	TATGTAACATATTAC[A/G]TATTATGTGATATGT	10529
rs182705091	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21090526	CTTGATGTTCTGGAA[C/T]CTACCCCCACAGATA	10529
rs182705578	snp	C/G	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:20894816	CGCCTGTGGTCCCGG[C/G]TACTCGGGTGGCTGA	10529
rs182710468	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21076545	AAAGTGGGAACTCAA[C/G]CAAATATTTATACAT	10529
rs182715390	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21040030	ACCAACTGTTAGTCT[A/G]TTTGTGTTGATATAA	10529
rs182723748	snp	A/G	0.000838632	0.02046	intron-variant	NEBL	GRCh38.p7	10:20831349	CTTTGCTTAAGCTTT[A/G]ATAGCGATGTTGAAA	10529
rs182726011	snp	C/T	0.00478085	0.0486577	intron-variant	NEBL	GRCh38.p7	10:21004209	ATTTGGTAACAACAG[C/T]GTTGTTTGAAGAAGT	10529
rs182727673	snp	A/G	0.00676609	0.0577691	intron-variant	NEBL	GRCh38.p7	10:21024553	GAGAAAGAGTGGGAT[A/G]GCCTCATGAGTTGAG	10529
rs182730532	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20881659	TTAGTTTATGTATAA[C/T]TACTTATCTATCTTC	10529
rs182734594	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21072818	CAACATGATAAAACT[C/T]CGTCTCTACTAAAAA	10529
rs182741646	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20864405	TTACAACTACGGGAG[C/G]AAAGCTATTGTAGAA	10529
rs182745765	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21057354	GGTAAAACAAAAAAG[C/T]AAGATGTGGAAAACA	10529
rs182745991	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21086201	GTTATCATTTAGGCC[A/C]ACATGAAATAGAGCC	10529
rs182760164	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20864880	GCTTTCCCCTTTTCT[C/T]GTGAGTTTTATACAG	10529
rs182762276	snp	G/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20849579	CATCTCCTCCTCTAA[G/T]GCATGTGCAAGCACT	10529
rs182763613	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20782503	TTCCCAGAGTGTTGT[C/T]AAGCTCAGCATGGAG	10529
rs182776171	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NEBL, LOC102725112	GRCh38.p7	10:20845093	AACACACACTTTCTT[C/G]TTTCTAATGAAAATG	10529
rs182787408	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21092009	ATTTAACCCTATAAC[A/G]TATCTTTTTCTTCTA	10529
rs182805388	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21152285	TCTCATAGATTGGAC[C/T]CCAAGGACAGTGACG	10529
rs182814393	snp	G/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	NEBL	GRCh38.p7	10:20813312	AGTATGCAATAAAGT[G/T]ATATCTATTTCCAGG	10529
rs182817304	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21124053	AAACCACTGAAATAC[C/T]TCTTGGTATTTGTAG	10529
rs182836278	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21112663	TGATGGGTGTAGCAA[A/G]CCAACAAACATGGCA	10529
rs182842123	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21161805	TGAAGCATGCCTGTT[G/T]TATAATAAAGAATTT	10529
rs182849330	snp	A/C	0.00874735	0.0655527	intron-variant	NEBL	GRCh38.p7	10:21103844	TATACTTTTTGAGAC[A/C]TATTCTTAAAATGTT	10529
rs182873971	snp	A/G	0.00478085	0.0486577	intron-variant	NEBL	GRCh38.p7	10:21166651	TCATACAGCCCTGTG[A/G]GTTTAGTATTACTGT	10529
rs182887353	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20781801	TGGAATACTTCAGAG[A/G]CTTTTATTTTAGCAT	10529
rs182891912	snp	A/C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21160771	ATTCTTCCACAAGAG[A/C/T]CTGTTAAGACCTTTT	10529
rs182893458	snp	A/G	0.00199481	0.0315187	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21144742	AAAAAATGAAAAAAG[A/G]AAAAAAGGCAGATTG	10529
rs182896797	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20797951	CAAAAAAACAAAAAA[A/G]TACTCACCAGGCATG	10529
rs182906215	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21072288	CCTCTTTTCCAGTTC[C/T]GTCTTTTATAATGTC	10529
rs182911998	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21103502	ACAGGCATGAGCCAC[C/T]GCACCAGGCCTTTTT	10529
rs182912961	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20979882	CATCTAATTTTTAAA[C/T]AAAATTTTAATATAG	10529
rs182913178	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20960072	GACTAAATTTGAATA[A/G]AAATTAAAAGGCTTA	10529
rs182919778	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21056427	AAAAAAAGATAGACT[A/G]ACTGTCCTCCCGGAA	10529
rs182921904	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20943242	GGCACATATACACCA[C/T]GGAATACTATGCAGC	10529
rs182947848	snp	A/T	0.00358779	0.0422022	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21140236	CTTTGAAAATGTGCC[A/T]GATTTGAATTGATTT	10529
rs182951749	snp	A/T	0.00438332	0.0466095	intron-variant	NEBL	GRCh38.p7	10:20787574	TTGCAGATGCTCAGT[A/T]AAAAACATAAACAAA	10529
rs182952601	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21106724	CCAATTCTGTGAAGA[A/C]AGTCAGTAGTAGCTT	10529
rs182959246	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:21122846	CATCCACTTATACCC[C/G]CTTCAAGTATTCCCT	10529
rs182965275	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20801761	CTCTTGATATATGCT[A/G]TGAACAATAAACTGA	10529
rs182974344	snp	A/G	0.000527792	0.0162363	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20880762	ACTTAACTACAGTTC[A/G]CTAGAAAATCATGAG	10529
rs182977388	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20878503	CAGGTTTATGGGAGA[C/T]TGTCTTTTATAGAGA	10529
rs182989482	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20906865	TCTAACTTTCTCTCC[C/T]ATTTCAATCATACAT	10529
rs182998195	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20911288	ATCAGGATCCCCAAA[C/T]TGAAGTTCAAAGTTA	10529
rs183005362	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20849153	GCACCCACAAAACTT[C/T]GATATAGGCTGCAGA	10529
rs183010725	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20794703	ACTCTACTTCCCCAG[C/G]AATACTGAATCTGCA	10529
rs183032096	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20911383	CAGTTAAATGTATAT[A/G]CCCGTTGTGAGCATT	10529
rs183048081	snp	A/G	0.00517822	0.0506191	intron-variant	NEBL	GRCh38.p7	10:20974838	GACTTTTAAAAATTA[A/G]CGTGAATTTTCAACA	10529
rs183051034	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20816761	TCAACAACAGGGAAT[C/T]GGAGCAGGCCACAAG	10529
rs183076565	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20860335	TCTGAAATGTCCTGG[A/G]TCAACTTAATGTCAA	10529
rs183089627	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20808409	TCTCAAATACAGCCA[A/G]GATAGATGTTCATGC	10529
rs183095752	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20840506	TCTCATTAAACTATT[A/T]TCGTTTATTATATGG	10529
rs183099284	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20798801	CCTTCACACACATAC[A/G]GAACCCTTTGACTGA	10529
rs183100462	snp	A/C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20824225	ATAGGCTCAACTTAA[A/C/G]AGGCCGTGTTGAAAT	10529
rs183109151	snp	A/C	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21141225	TTCATTTAGTGAAAT[A/C]TGAACGAGGTCTGTA	10529
rs183113057	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21155514	TTTTTAGATCCCACA[G/T]ATAAGTGATAACATA	10529
rs183114768	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20829286	TTCATGTCCTTTGTA[A/G]GGACATGGATGAAAT	10529
rs183121582	snp	A/G	0.0103295	0.0711199	intron-variant	NEBL	GRCh38.p7	10:21069327	ATGGGGCCGTTTATG[A/G]CAGGCACACAATTCT	10529
rs183122505	snp	A/C	0.00438332	0.0466095	intron-variant	NEBL	GRCh38.p7	10:21101348	CAGATCACGTGCAGG[A/C]AATGTGGTCAAGTAA	10529
rs183126625	snp	A/G	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:20794330	CTAGACTCTCATATT[A/G]TCTTTGTTTTAATTT	10529
rs183131201	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20914898	AGTCTCACTCTGTCA[C/T]CCAGGCCGGAATGCA	10529
rs183147737	snp	A/C	0.00119737	0.0244387	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21136673	ATGCTTTCTACCCTA[A/C]GGCTGGACAAAGCTC	10529
rs183151049	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20929064	AAGGTTGGAGATCTT[C/T]GAGAAACCTCCATAC	10529
rs183152948	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20870454	TGTCTTTGTATCTAA[A/G]TGCATATATTTATAT	10529
rs183159580	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	NEBL, LOC102725112	GRCh38.p7	10:20885125	ATTAGAACCCAGAAT[A/G]TCATTAAATTTCTGA	10529
rs183163622	snp	C/T	0.00676609	0.0577691	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20898890	GGAAACATTGCTCTA[C/T]TCTCCTAAAATGTTG	10529
rs183195544	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21039510	GTTTTTGTCAGGTTT[A/G]TTGAAGATCAGATGG	10529
rs183220669	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20980633	CTAGAACAGAGAGAG[C/T]CTCTATACCTCAAGA	10529
rs183227250	snp	A/G	0.00557542	0.0525036	intron-variant	NEBL	GRCh38.p7	10:21036032	GCTGGGCATGGTGGC[A/G]CGCACCTGTAATCCC	10529
rs183240180	snp	A/G	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21045126	TAAAATTAAAACTGT[A/G]TCTTTAAAATTGCTG	10529
rs183243450	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21080432	CATTTGGGACTAACT[C/G]TGGCATATAAGCTGG	10529
rs183262781	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20935483	GAACATGCTCCCCTC[A/G]GTAGTGAGCCTTAAA	10529
rs183263109	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20891670	ATAGCTCAGTCTTAA[C/T]TGTAGACTCTATTTT	10529
rs183288859	snp	G/T	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:20923537	CACAAAAATTAGCCG[G/T]GCATAGTGGCACAAG	10529
rs183292282	snp	G/T	0.0138799	0.0821421	intron-variant	NEBL	GRCh38.p7	10:20952313	GTGGTGCCAGGCACC[G/T]GTAGTCCCAGCTACT	10529
rs183294135	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21016873	ACGTTTTTGCAAAAA[A/T]GGAAATATTCTTACA	10529
rs183296503	snp	G/T	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20990973	TGGGCACTCTATTTT[G/T]CACGCTGTCCATCAA	10529
rs183302203	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20956157	CAGGTGTAAGGGAAA[C/T]CACAGATTTGGAAAC	10529
rs183304834	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20982645	GCAAGAACTGACAAG[C/T]ATCTTACTTATACCT	10529
rs183306568	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20999273	TGTGAGAAGACCTGC[A/G]GTGATGCTATATTCT	10529
rs183314860	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20921182	ACTGTGAAGCCAACA[C/T]AGAGTAGTGCTGATC	10529
rs183315025	snp	A/T	0.00557542	0.0525036	intron-variant	NEBL	GRCh38.p7	10:20955382	TCAGAGATGAGACAC[A/T]TCACTGTAGCTGGGT	10529
rs183317775	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20986837	CTCTCTCCAAATAGC[A/G]TCAGAATAATAAATC	10529
rs183318432	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21035364	ATATTTTACAACAGT[A/C]TGTGTTAAAGAAAAT	10529
rs183324965	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21014123	TTTCCTATTTTTTAT[C/T]ATTATTAATATTATT	10529
rs183325963	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20891211	CTGTGACTCTTGGAT[A/G]TCAGATGCCTACCAC	10529
rs183328178	snp	A/T	0.00245847	0.0349741	intron-variant	NEBL	GRCh38.p7	10:20823176	TTGATATACAATAAA[A/T]TTTTTAAAAAATACT	10529
rs183331485	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20911754	ATGTGTTCCAAAATC[A/G]ATATAAACATCATCA	10529
rs183332609	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20906583	TGAGAACTAGTTTAA[C/T]GTATATTGGGGTGAT	10529
rs183337607	snp	C/T	0.0883596	0.190715	intron-variant	NEBL	GRCh38.p7	10:20894927	GAGCGAGACTCTGTC[C/T]AAAAAAAAAAAAAAA	10529
rs183341553	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20920091	AAGAGAAATATAAAT[C/T]AAAAGAACATGACAT	10529
rs183347239	snp	A/C	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20940125	ACCCCAAATCAACAG[A/C]ATATACATTCTTCTC	10529
rs183350398	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20865870	AGCAGTTGTGTCCAC[C/T]TCATTTTCATTCCTA	10529
rs183352229	snp	A/G	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:20820594	AGTTTGGAAGGCCGA[A/G]GCAGGTGGATCAACT	10529
rs183354094	snp	A/T	0.00199481	0.0315187	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20859099	TACTTGAGAAGGAAA[A/T]CTAAATATTTTCAAC	10529
rs183355819	snp	A/T	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20805088	GTCCAGCTGACAAGA[A/T]TTGCCAATGAACTAG	10529
rs183357433	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20924067	TCGATATACAGCAAT[A/T]CTTGGACAATGAATA	10529
rs183357851	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20965376	GGTGGTCAGGGAAGT[C/T]CCCAGTAAGAAGGTG	10529
rs183358091	snp	G/T			intron-variant, upstream-variant-2KB	NEBL, LOC102725112	GRCh38.p7	10:20844389	TTATATTGTGTATAA[G/T]ATATATATACAAATA	10529
rs183362548	snp	A/G/T	0.00398564	0.0444627	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20882497	ATGAGCTCCTTGGGC[A/G/T]CATGTCTGTCTCACA	10529
rs183364694	snp	A/C	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:20895205	ACCACTTTAGTCCTG[A/C]TGGTTTATGTAACAC	10529
rs183369071	snp	A/G	0.0023933	0.0345097	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20878215	TTTCTGCTTACTCAC[A/G]TTACTAAAGGCACAA	10529
rs183370913	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21084022	ATCTTGGGAAAAAAA[A/C]CCTAGTATAAATAAC	10529
rs183373773	snp	C/G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20793815	TCCACCTTGGCCTCC[C/G/T]AAAATGCTGGGATTA	10529
rs183383880	snp	C/G			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21144414	GAGCCTCCCAAATAA[C/G]CCCCTCTTGCTCAAA	10529
rs183388268	snp	C/G	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:21087525	TAAAACTGCCTCTAA[C/G]AGAATTCACAATCCA	10529
rs183394554	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20980531	CATGTACATATATAG[C/T]GTGCATGGTACAAAC	10529
rs183397710	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20960867	TGACTTTATAAGTGA[C/T]GCACAAAATACAGTT	10529
rs183398130	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21104828	GGAAAACTTTCTGTC[C/T]TTCACCATCAAGTAA	10529
rs183399339	snp	A/G	0.00716266	0.059414	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21140764	CATGGACACAGAGAG[A/G]GGAACATCACACATG	10529
rs183404696	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21115423	TCTGTTAACATTTCC[C/T]GTACTGATGGTCAGC	10529
rs183416285	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21120387	CTCAAAAAAAAAAAA[A/T]AAATACATATATATA	10529
rs183445910	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21051226	CGAGGATTTATATTC[A/G]GAGATCACATTTTTT	10529
rs183458411	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21018091	CCTCCCAAAGTGCTC[A/G]GATTACAGGCATGAG	10529
rs183461471	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21152383	TCCATTTCCCAAAGT[C/T]ATACAATGCCCCTGG	10529
rs183484931	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21064691	GTACAAGCCATGTTT[A/T]TACCATATCAAAATG	10529
rs183491937	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21094755	GAATATTACAGACTC[C/T]TGTTAACATCAGATG	10529
rs183513238	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20937782	AGCAAACGGCACACC[A/G]GGAGATCATATCCTG	10529
rs183515191	snp	A/G	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:21061447	TGTATGATATATATC[A/G]TATATTACATGATAT	10529
rs183527392	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21091079	TCCTGAACCTCTCTC[A/G]GATTCGTCTGTGTAT	10529
rs183534448	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21014369	CTCATCTGGTTTCAC[C/T]CACTGCAGGATATCC	10529
rs183537531	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21032606	CGGTGAATTAGAGCA[C/T]GTAAATGGGGAATGC	10529
rs183549250	snp	A/G	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:20994891	GGAGGTAGAGGGGGG[A/G]GTTGGTCTTGCTGTC	10529
rs183553541	snp	C/G/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21031749	CGGGAGCCCAAGTTG[C/G/T]AGAAGACCTGAACCC	10529
rs183556287	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20892713	AATTTAGTGCAGGGT[C/T]GCTTCCTCCTCCTGG	10529
rs183557338	snp	A/G	0.00597247	0.0543191	intron-variant	NEBL	GRCh38.p7	10:20972608	AAAAATTAGCTGGGC[A/G]TGGCAGTGCGCACCT	10529
rs183559361	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21152867	CTTGAAAAAAACAAC[C/T]GTACATCAATTTCCT	10529
rs183561022	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20994529	TTACTTCCATTGGCC[A/G]TAATATAAAAAGCCA	10529
rs183563031	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	NEBL, NEBL-AS1	GRCh38.p7	10:21172841	TCCAGTTCAAAGTGT[C/T]TAAATGCAGGGTTTG	10529
rs183586302	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20840029	TGAGTGAAGACATCT[C/T]CTTTGATGCCTACCC	10529
rs183596121	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21085051	GGCTTGTCACATTCA[C/T]TGTGCCTGAATAGCT	10529
rs183599561	snp	C/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21010183	AGCTCCTCTGTATAA[C/G]GGATCACAGAGACAT	10529
rs183602493	snp	A/G	0.00636936	0.0560724	intron-variant	NEBL	GRCh38.p7	10:20807787	TAAAATATAACTGCA[A/G]TGAGGTGAGGAAACA	10529
rs183607273	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20836616	CTGGGAAGAGCATGC[A/G]CTGGGGTGGAGCCAC	10529
rs183610012	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21102481	TTTCTGTTGCTATAG[A/G]TTCAATTGCATTTCC	10529
rs183610526	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21029389	TTACCACGTGAACCC[A/C]GCAATCCAGAGAGGT	10529
rs183615495	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21119877	TATCTCTTCAATCTC[C/T]TTTAAACAGCTCCCC	10529
rs183616020	snp	C/T	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21138181	AACAGTCTTATATTA[C/T]TGGGACAACGGACAG	10529
rs183617715	snp	C/G	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21116560	CAGTCCATAGCAGTC[C/G]TTGTCTAGTAATTCT	10529
rs183620424	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20991613	TGTTTTTAATTTTTT[A/T]AATTTTTTTCTATTT	10529
rs183632553	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20804641	GCAGAAGTATTCCAG[G/T]CTGGGGGAACAGTGT	10529
rs183635749	snp	G/T	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:21082345	ATAAATAAATATTAG[G/T]GTTCTGATTTGGATG	10529
rs183638700	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21067267	TGAGCCACCGCGCCC[A/G]GCCGAAATAATTTAA	10529
rs183642759	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21112140	CTTTTACATGGTTGG[C/T]GGGAGTGTAGATTAG	10529
rs183644377	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21098430	ATATGGTACCAAATG[C/T]AGACTCAGGAAACCC	10529
rs183650004	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21155238	TCACATCATGGAAAA[C/T]GGGGTATCCATCCCC	10529
rs183651776	snp	C/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20850642	AGGTTGAGCACTGGG[C/T]TCCCTTTGGTTAATG	10529
rs183652526	snp	A/C	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21131652	CAAATCCATGTAGAA[A/C]CTCTGGTGTGTATGA	10529
rs183653141	snp	A/C	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:20905156	AGAACTATAACTTAC[A/C]CAAACACATGAAAAA	10529
rs183653740	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20874342	TGCCAGATACCCCAT[A/C]CATTTGGAAACCATG	10529
rs183664186	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20919206	GAGATTAGTCTCTCA[C/T]GATTTCCGAGAAAAT	10529
rs183676912	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20977203	ATAGAAGCCGGAAGT[C/T]AGCACGTCACATTCA	10529
rs183680631	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20933784	TACAATAAAGCCTCA[C/T]GGTTTGGTGAATTCA	10529
rs183683191	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20877432	TTAGGCAGATAGTGA[A/G]GGTAAGGAAGTCCTT	10529
rs183686388	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:20957128	ACCGAACTTTGAATC[A/T]AATCTTTTAATAGCC	10529
rs183687618	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20890257	ATTAGCAAGCATGTG[C/T]CATCTCGCTCCTACA	10529
rs183691713	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20940842	AAAATCTAGAAGAAA[C/T]GGATAAATTCCTCAA	10529
rs183702573	snp	C/T	0.000798403	0.0199641	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21137522	CCGTGTCTAAGAACA[C/T]TACGGCTACTGCTGC	10529
rs183707365	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NEBL, NEBL-AS1	GRCh38.p7	10:21172241	ACAAAGTACATGGCC[C/T]CAGAGTCTGTGATAT	10529
rs183737432	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21042832	AGTACACATTCATTT[C/T]GATTAACAAAAACAA	10529
rs183738057	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20817836	CACGCTTACATATAC[A/G]CCCACATTCCGATGG	10529
rs183742909	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21076677	ATCAGCTACTATTCA[A/G]CCTTAAAAAGGAAAG	10529
rs183754437	snp	C/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21150871	CACCAACTTCTTCAA[C/G]CCTGGCTGAAGAACA	10529
rs183764229	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20802159	TACGAATACTTTCAA[C/T]ACCAGAAAACTGCAA	10529
rs183766104	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21168051	GTGTACTATACTTTG[A/T]TCGTTCTATCAAAAG	10529
rs183770506	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20789075	ACAATTGCTCTCCTG[G/T]AGCACCGAGGGTCTT	10529
rs183778907	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20991209	TTGGCTCTCTGACTT[A/G]ATGAAGAATGTATAT	10529
rs183786824	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20907375	ATGCTATCTTGTTTC[A/C]TTAATGAAATGACGT	10529
rs183799006	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21028780	CAATATAATTTAAAA[A/G]AAAAAATGAAGACAG	10529
rs183804061	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20784128	TTCCTTGAATATAAC[A/C]TATAAGGCAGATATC	10529
rs183807113	snp	C/T	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:20805279	ATATGTCACTAATCA[C/T]TTGAATACTGACATC	10529
rs183814738	snp	A/G	0.00716266	0.059414	intron-variant	NEBL	GRCh38.p7	10:20799729	AGTAGTCAGAAAACC[A/G]AAGCAGTGGCTAAAA	10529
rs183815601	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20932923	TGCCCTTGCATTGAT[C/T]TGAATACTTGCATAA	10529
rs183816084	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20837353	GTCAAACCAGACAAA[A/C]CATTCCAGACACAAC	10529
rs183816301	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20821019	TATGTAGTTTGAGAT[A/G]TTACGCAGATTCTTG	10529
rs183819789	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20820071	AAATTGCCATTTTAT[A/G]TTTAAAAATAATAAT	10529
rs183823956	snp	C/T	0.00119737	0.0244387	intron-variant, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20853106	AAGGAATAAAAAAGT[C/T]CTATACAAAAAGACT	10529
rs183847252	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20902936	ATAGAAAACAAATTA[C/T]TGAGTGTTCCCTTCA	10529
rs183852233	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21025560	ACCTCGTCAGAGCTC[A/G]TCAAAATGCAGGAAG	10529
rs183857568	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20791506	ACTCCTGGACTCAAG[C/T]GATCCTCCTGCCTCA	10529
rs183859576	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20855204	ACTGCACTCCATCCT[A/G]GAGACAGAGCGAGAG	10529
rs183860428	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20987927	TTCTTTCACATGAAA[C/T]TTATATTCCATGGTA	10529
rs183860597	snp	G/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21005069	GAGAGTAACACCTTA[G/T]GCCCTCCATTTTGCA	10529
rs183862365	snp	C/T	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:20833709	TGCAGTGAGCCGAGA[C/T]TGCACCACTGCACTC	10529
rs183872697	snp	A/T	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:20889229	TCACCACAGAAATCA[A/T]CATCGTTAACATTGT	10529
rs183874852	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21040645	CACCTCCCACCAAAC[C/T]CCACTACCAACCTTA	10529
rs183878846	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20970885	AAAAAAATGCCAAAG[C/T]GAAAAATATCAAAGT	10529
rs183889743	snp	C/G	0.0322114	0.122752	intron-variant, upstream-variant-2KB	NEBL, NEBL-AS1	GRCh38.p7	10:21173283	TAGCAATGCGGCAGC[C/G]GCCGCCCCATGACAT	10529
rs183898857	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20858017	CACTTTGAAGTATAG[C/T]TGTATGCAGGAGATA	10529
rs183924659	snp	C/T	0.00517822	0.0506191	intron-variant	NEBL	GRCh38.p7	10:20915306	CATGTGCACATTGTG[C/T]AGGTTAGTTACATAT	10529
rs183930943	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20943357	AAAAAACCAAACACC[A/G]CATGTTCTCATTCAT	10529
rs183943206	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20853606	TGTGGGAGCTAAAAT[A/G]GTGAGACCCCAGTTC	10529
rs183944013	snp	A/C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20885881	TCACCCATGCAGAAC[A/C/G]TTGACATCATATATT	10529
rs183947583	snp	C/T	0.0107246	0.0724382	intron-variant	NEBL	GRCh38.p7	10:20900793	TAGGTTGCAGTGAGC[C/T]AAGATCCTGCCACTG	10529
rs183956818	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20885583	GTTAAGTTCTATGTT[G/T]CAGGGATTTGTGTAT	10529
rs183957730	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20915484	TTGTTCAATTCCCAC[C/T]TATGAGTGAGAATAC	10529
rs183962415	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20976108	GGGAGGCCAAGGGAG[A/G]CAAATCACTTGAGGT	10529
rs183969580	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20853657	GCTGGGCATGGTGAC[A/G]TGCACCTATAGCCCC	10529
rs183980045	snp	C/T	0.0023933	0.0345097	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20871690	AACATCTGTTTTCTT[C/T]CACATTTATATTTTC	10529
rs183998936	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21095563	ATTTTGAAGCTAATC[G/T]GATTATTTAGGATGT	10529
rs184004974	snp	G/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21009296	ATATTTAGTTGTGTG[G/T]TGTCTAAAATACTGT	10529
rs184020626	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20851903	AATGAAGGTGAGTAC[A/G]AAATTATTATGGACT	10529
rs184026365	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20903898	GGGATTAAAATCTAC[A/G]GATTGGGAACAATTA	10529
rs184026492	snp	C/T	0.00199481	0.0315187	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20867313	AGTACGTCTTTTCAT[C/T]TGTTCGGGACTTATT	10529
rs184027995	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20883676	TTTATTTTGTACTTT[A/C]GACCTACTAACATAT	10529
rs184028560	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21124482	CAGTTTCTCCCTGAG[A/C]TGTCTAAAGACCCTA	10529
rs184031179	snp	A/C	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:20918355	AGAGCAAGACTCTGT[A/C]TCAAAAAAAAGAATC	10529
rs184034711	snp	A/T	0.0154538	0.0865337	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21128158	AAACACAAACAGTAA[A/T]TTTTTTTAATTCTTA	10529
rs184036011	snp	C/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20803057	CAGGGTTCCGGCCAC[C/T]GCAGGACACCACTGC	10529
rs184038073	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20917989	ATAAAATAACAGGAT[C/T]CAAAATGATATATGC	10529
rs184038726	snp	A/G	0.00159617	0.0282053	upstream-variant-2KB, intron-variant	C10orf113, NEBL	GRCh38.p7	10:21146752	TACAAAAGTATTCAC[A/G]AAACTTGGGCTATGA	10529
rs184041425	snp	G/T	0.0162398	0.0886349	intron-variant	NEBL	GRCh38.p7	10:20946470	TGTTTTTTGTTTGTT[G/T]GTTGGTTTTGAGACA	10529
rs184047485	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21165801	GAAAGGTGTGGGGTC[A/G]GGTGTGATGGGCACA	10529
rs184050883	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20834577	CCTCTGGCCTTCCAG[A/G]TTTCCTGTAAGGTGT	10529
rs184055589	snp	G/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20929699	GGGAGCTAAATAATG[G/T]GTACACGTGGACATA	10529
rs184057135	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20818443	CCCAGCACAGAGTAG[C/T]GCTGCCTTGTTAACT	10529
rs184062115	snp	C/T	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20951254	ATTTCACAAAAGCAA[C/T]AGGTCCTTCAGACAG	10529
rs184082341	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20900053	CCTCATGGACAGCTA[C/T]CATGTTTCAAAATCC	10529
rs184091887	snp	A/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20985533	GATCAAAAAAACTCA[A/T]TACCATGAAATCTCA	10529
rs184099962	snp	C/T	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:20984387	GAATGGAATGTTGTT[C/T]ATGTTTTTCATGTAG	10529
rs184103694	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20973563	ACTACCATTTTTTTA[C/T]ATAGAAAAAATGTAT	10529
rs184106121	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20871012	ATATTTGCCAGATGT[A/G]GTTCTATTTGGCAAT	10529
rs184110440	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20953167	ACCACCAATGTGACT[A/G]TATTTGGAGAGGGTG	10529
rs184114790	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20938667	GGAAGTTCGAACCCA[C/T]GGCAAAGAAGTTAAA	10529
rs184130519	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20949735	TTTGATTTCCTTTTG[C/T]GTTTTGTTTTTTTTC	10529
rs184130959	snp	A/G	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20836712	TTCAAACTGTGAGGT[A/G]GGAAGCACTCTAGCA	10529
rs184147072	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21018905	TGGTAGCAGGCGCCT[A/G]TAATCCCAGCTATTG	10529
rs184162565	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21080720	ACAGATCTAGAAGGA[A/G]GTGTCCAACCTGTTT	10529
rs184163404	snp	A/C	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20924883	GAGGGGTACATGGTC[A/C]CTGAGGTTTGTAACT	10529
rs184170121	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20996383	TGTCACTTTATAGAC[A/G]GCGAAGTGAAAATGC	10529
rs184172060	snp	C/T	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:21109661	GTAGGCTATTAATTA[C/T]TGCCTCAATTTCAGA	10529
rs184178575	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20895741	GTATGATTTCCACCA[C/G]CATCCTTTGTGCTTG	10529
rs184179418	snp	A/G	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20981272	AGGCACAGTCTACCC[A/G]AAATGGCTTCAAACA	10529
rs184182361	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21148606	TCTCAGCTCACTGCA[A/G]CTTCCACCTCCTGCG	10529
rs184232415	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20962224	TTCTCCTCCTGTGCC[C/T]GCCTGTCAGTGAAAA	10529
rs184238722	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20944697	ACCATTGCCCAATTT[A/T]CAAACCACACAGACA	10529
rs184241861	snp	A/C	0.0123036	0.0774623	intron-variant	NEBL	GRCh38.p7	10:20900990	GCCACTGCACTCCAG[A/C]CTGGGTGACAGAGCG	10529
rs184243005	snp	A/G	0.00199481	0.0315187	upstream-variant-2KB, intron-variant	C10orf113, NEBL	GRCh38.p7	10:21147648	CCACGGTTCAAGCCT[A/G]CATCCCTGAGTAAGA	10529
rs184244358	snp	C/G	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:20930609	TTCCCCTTTTGCTCA[C/G]TCCAGCTTTCTCTCC	10529
rs184247102	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20915920	ATCCAGGTATTCAAC[A/G]AACATTCTATTTAAA	10529
rs184267920	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20968606	TAGACAAGTGCAGTG[A/C]GAACTATGCAAGGAC	10529
rs184268040	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21022047	GTGAGGAGATGGCAT[A/T]TCCTCCCTGTGTGCA	10529
rs184272784	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21062319	TGAGGTAGAAAGAGA[C/T]GATATTTTAAATGAA	10529
rs184278641	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21037373	CCATTCAAGAGGATA[A/T]GACATTACATGATTT	10529
rs184284559	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21043952	CTAAATAGATCCACA[A/G]TGTGCATATGGCCAC	10529
rs184285652	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21001202	GCCAGCCGACAGACC[A/G]CCAGAGACAAAAAGC	10529
rs184287554	snp	A/G	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:21092708	TAGTTCCAGTTCTTC[A/G]AAGCACTTTTTAACT	10529
rs184292414	snp	A/G	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:21077692	AGAATTCAGCTGATG[A/G]TCTGTTGGTTCCTGA	10529
rs184295563	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21107361	ATACCTAGTTTATTG[A/G]GAGTTTTTAGCATGA	10529
rs184297266	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21037542	GGGTCGGGTGACAGT[C/T]AGGGCAGGTTCACCA	10529
rs184316314	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21053332	AATCCCACTTCCCAC[C/T]CTTTTAAAATCCTGG	10529
rs184337560	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20912352	GCTACTCCAGGAGGC[C/T]GAAGTGGGAGGATCA	10529
rs184342321	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21101536	GGGAAAAAAGAAAAC[A/G]AGCCTGGGTCCCTAA	10529
rs184358132	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21088885	TCTAGAAGAGCTGGA[G/T]ACTTTCTGGAAGAAC	10529
rs184363887	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21120782	CTGAGGAAGAACACA[C/T]GCCCAAGTGAGGTCT	10529
rs184375448	snp	C/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21026202	ACTGTCCTCAGAGGA[C/T]ATTTGGCAATAGGCA	10529
rs184380918	snp	A/G	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21125703	CTCCTTCCTCCCTGC[A/G]CCCTACAGAGCTGCC	10529
rs184384866	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21036540	TGATAGTCAATGAAT[A/G]GGAGCAGATTGATAG	10529
rs184390600	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21156308	TTTGTACAAATGGAC[A/G]AAGAGTTATCAAAAA	10529
rs184390801	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21052962	CACAGTAGGGTGACT[A/G]TAGTCACAACAATAT	10529
rs184396054	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21163412	CTACTTATAGGGCAC[A/G]TCTTTCTGCACTGAG	10529
rs184398616	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21018786	TGTAATCCCAGCACT[C/T]TGGGAGGCCGAGGCA	10529
rs184418224	snp	C/T	0.000190749	0.00976412	intron-variant	NEBL	GRCh38.p7	10:21069918	ATTTTCCCCTGATAG[C/T]GCAAGTCATGTAAAT	10529
rs184419968	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21084814	AGGGGCATACGCACT[A/G]GCACAGAGAGAACCC	10529
rs184422278	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21070506	TGGACTAAATCATGC[A/T]GTTTTAAAGAGTACA	10529
rs184439363	snp	A/G	0.00914312	0.0669923	intron-variant	NEBL	GRCh38.p7	10:21167106	CGTTCTGGGTGACTC[A/G]TCACGAGATGCACCC	10529
rs184448442	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21058829	TGAAATCAATCATAG[C/T]TCATTTCCTTAACTA	10529
rs184461799	snp	A/G	0.00478085	0.0486577	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20867036	TTAAAATATTAAAAT[A/G]TTCTCATCAAATGCA	10529
rs184489501	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21059461	AATCACTTTCTAGTA[C/T]CAAAAGGCACTTCAA	10529
rs184498575	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21105136	CTAAAAGTCTGTTAA[A/T]AACTTTTACATACGT	10529
rs184499999	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20833966	CTATGCTTTGGTTGG[C/T]GCCATTTGAAGATTG	10529
rs184506041	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21041121	ATGGGTAGACTGTAT[A/G]TCATGGGGGTTTGGT	10529
rs184512447	snp	C/T	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21142065	AATCACTCTCTGTAA[C/T]AGGACAAAAGACCTC	10529
rs184514987	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21089902	TTGTAGCACTGTGCC[C/T]TCTTTTAAATTTAAA	10529
rs184515083	snp	C/T	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21129601	AATGAGAGGGAGGAA[C/T]TAGAAGAATTAGAAT	10529
rs184521305	snp	G/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21074589	TTCAAGCGATTCTCC[G/T]GCCTCAGCCTCCCTA	10529
rs184532603	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21105383	GATGTTTCCCACCCT[A/G]GGTCCATGTGTTCTC	10529
rs184533774	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21149921	AAAATCCCTCACACA[A/T]CTGGTCACAGAATTC	10529
rs184559684	snp	C/T	0.00159617	0.0282053	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21125405	AACAACTGTTTTAAA[C/T]TGGGGGTTGGGGAGA	10529
rs184570308	snp	C/T	0.00159617	0.0282053	upstream-variant-2KB, intron-variant	C10orf113, NEBL	GRCh38.p7	10:21147321	TCTCAGAAGAAGGGG[C/T]CCTCATCAGCAGAGA	10529
rs184573151	snp	A/C	0.02016	0.0983543	intron-variant	NEBL	GRCh38.p7	10:21073614	AGAGCAAGACTCTGT[A/C]GTCAAAAAAAAAAAA	10529
rs184582428	snp	C/G	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20827202	AGGTAAATGAGGATA[C/G]AATTACTCCCTTTCT	10529
rs184586514	snp	A/C	0.00199481	0.0315187	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20851576	ATCAGGAGTTTGAGA[A/C]CAGCCTGGCCAATAT	10529
rs184587899	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20792067	AAAGAAAAGGTGAAG[A/G]TTTTGAAGGCCCCTC	10529
rs184592972	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20883061	AACACCTTACATGCT[C/T]TCTTCAGCCCAAATC	10529
rs184598704	snp	G/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21103012	GCCCCAGTGCATATT[G/T]TTCCCCTCCTTGTGT	10529
rs184620929	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21162207	GCAAGGACAGGGAAG[C/G]CCCATATCCAGGATC	10529
rs184631799	snp	A/T	0.00119737	0.0244387	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21138597	AATGGGAAGTGTGAA[A/T]AATAAACATTATTTT	10529
rs184634843	snp	A/G			intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20958826	AGCTACCCAGAAAAG[A/G]CAAGTTCACCCACTC	10529
rs184642343	snp	C/T	0.0185938	0.0946107	intron-variant	NEBL	GRCh38.p7	10:21001056	GAAACCAATGCAGGT[C/T]CCCATGAGCTTGTAT	10529
rs184642528	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20983961	AAAGTAATGACCCTA[A/C]TATATCTATTTTGCA	10529
rs184650274	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20962065	CTATTTAAGAGGTTG[C/T]AGGGATGGGATCAGA	10529
rs184653174	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20913565	ATGAAAAAATGTTCA[A/G]TTTACTGGAAATAGC	10529
rs184655308	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20926620	TCCAGGAAAGAAATC[C/T]GTCCCTCATTCATTG	10529
rs184666036	snp	G/T	0.00835141	0.0640778	intron-variant	NEBL	GRCh38.p7	10:20829449	TGTGGGGTAGGGGGA[G/T]GGGGGAGGGATAGCA	10529
rs184672858	snp	A/C	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	NEBL, LOC102725112	GRCh38.p7	10:20845610	AGTGAGGCTTCCTAA[A/C]ATCTTACTAGCCTAG	10529
rs184673359	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20930397	ACCACCCTATCTCAC[A/G]TGTCTCCTGTACTCA	10529
rs184675548	snp	A/G	0.00199481	0.0315187	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20860393	CTAAATTCAGCAGGA[A/G]AACCATCTCCAATAC	10529
rs184680395	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20799006	CGTAACAGAATGAAC[A/G]AATACTTGCGAACAA	10529
rs184682525	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20908323	TTCTGGTAGTGATAT[C/T]ACTTTCTCTCATCTC	10529
rs184686082	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21163121	AAAGCTAGCAGCCCA[G/T]TGTGGCTGGAGAGAA	10529
rs184693623	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20783034	AGGTGCATGCTCTCT[A/G]TGCTTGGACATTTAC	10529
rs184696072	snp	C/G	0.00011715	0.00765253	intron-variant, nc-transcript-variant	NEBL	GRCh38.p7	10:20813906	TCCGCCCATTCCTTA[C/G]CATGTTTTAAGAATG	10529
rs184717879	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20879463	TAAACTATGTTAGAA[A/T]AGTGCTCTGCTTTTG	10529
rs184724575	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20796328	TGCACCATTGCACTC[C/T]AGCCTGGGGTGACAA	10529
rs184739390	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20809470	CTACCTTTAAAAAAT[C/T]ATAACAATGTATTTC	10529
rs184742827	snp	C/T	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:21085262	ACTAAGTCATAGCTA[C/T]TTTCTTCTCATTGTT	10529
rs184745965	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20814882	AAATACACACAGCAT[C/T]TCTGGACAGAAATGT	10529
rs184747073	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21117015	CAGAAATATACATGT[C/T]ACTTTGTTGGTGCTG	10529
rs184753999	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20846886	ATGCTTTTTGAAGAA[A/C]GCAGTATTTGTGAAA	10529
rs184772264	snp	A/G	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:21153056	TCCACCCCACATCAC[A/G]AGCCTTCTAGCTCAC	10529
rs184784074	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20912954	TTTGGTAGACACAGG[G/T]TCTCACTATGTTGCC	10529
rs184792808	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21034547	ACTTATTTGACAATT[C/T]GCAGATCAGTTATTT	10529
rs184800658	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21048882	GGCATGGTGGCAGGT[A/G]CCTGTAATCCGAGGT	10529
rs184801552	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21016042	GAAGCAGTTTTACTT[C/T]TGCTTCTTGTTGAAT	10529
rs184802387	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20921875	CACACACTCACATTC[A/G]TATATACACAAACAT	10529
rs184806210	snp	A/C	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:20944409	CTGTCTCATAATAAA[A/C]TAAAATAAATTATAT	10529
rs184807215	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20889593	TTTTCAAGAGGAATC[A/G]TATATAAATAAGAAA	10529
rs184826119	snp	A/G	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21067178	GGGTTTCACCGTGTT[A/G]GCCAGGATGGTCTCG	10529
rs184828970	snp	A/G	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21082137	CCAAACCGAAACTGA[A/G]GAACTTAACTGGGCT	10529
rs184840437	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20856616	AGAAATAGAGACACT[C/T]AAGGAATAGAGGAAT	10529
rs184848903	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20861612	CTTCAACAGCCTTCC[A/G]CTGGAATGACACTTC	10529
rs184857162	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20893737	TCTCAGTAAGGGAAA[C/T]GGCAAACTGAGATGA	10529
rs184859480	snp	A/C	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:20795713	AATGTGACTTCAACC[A/C]CATTCCCACTGAGTG	10529
rs184866064	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20996854	TAACTGTTTTTGTGC[A/C]AATATTTTTTCTCTG	10529
rs184870023	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20826203	ATCTAACCCTAGGTT[A/T]CATTAAAATGACCTA	10529
rs184873345	snp	C/T	0.00478085	0.0486577	intron-variant	NEBL	GRCh38.p7	10:20981769	CTGGCAGCCACCTTG[C/T]GACCATGAGGTAAGC	10529
rs184879883	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20830111	TCCCAGCGGCTGTGT[C/T]GGCTGCGGAGGCTGA	10529
rs184895390	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20842296	TTCGTGGTGTGACCT[A/T]CGGGAGTACTTTTAA	10529
rs184898909	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20826604	TCCTAGATCCGCTTC[C/T]TAGAAAGACAATTTC	10529
rs184910248	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20925601	AAAGAAAGCAATCTG[A/T]TTTCACACTAATTAT	10529
rs184913143	snp	C/G/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20857601	AGTTACGAGAGCTAG[C/G/T]GAAGTCAGGGTCCTG	10529
rs184914668	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20951716	TATATGGCCTAATTA[C/T]TAATGATAGTCACAT	10529
rs184915382	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20907843	CACAATTGGTACTTT[A/C]AAACTGCTGGAATCT	10529
rs184916084	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20891284	TTTATCTTATCTGAG[C/T]ACTAAATTACTTTTT	10529
rs184918460	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20993590	ACGGCAGCTATACAG[A/G]ACATGTTCTCACAAT	10529
rs184919896	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21071409	GTTGTTTTTCCCCTT[C/T]CAAAGCCCTACAAAA	10529
rs184920539	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20906670	GTGGGTGTGTCTATG[C/T]TCATTCAATCATTCA	10529
rs184924163	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:20979175	GTTATCCCAACACTT[A/T]GTGAGACAGAGGTGG	10529
rs184924540	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20935544	TTTGGCAGATCTCCT[C/T]CTTTGCAAGGATACT	10529
rs184926695	snp	C/T			intron-variant, utr-variant-5-prime, upstream-variant-2KB	NEBL	GRCh38.p7	10:20958984	GAAAAAATTTCAAAA[C/T]ATTGACATAGACATA	10529
rs184929932	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20920148	TCCAAAGTTTAACAA[C/T]GTATTCTGTTGGACT	10529
rs184941909	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:20938393	CCTGACTGTTAGAAG[C/G]AAAACTAACAAACAG	10529
rs184942567	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20941299	ACGCAAATCAATAAA[C/T]GTAATCCAGCATAAA	10529
rs184944883	snp	C/T	0.00517822	0.0506191	intron-variant	NEBL	GRCh38.p7	10:20841961	AATACTTACATACAA[C/T]TTATTTTTCTCTGCT	10529
rs184945343	snp	A/G	0.0023933	0.0345097	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20879170	CTTGACTAATTGACA[A/G]TAACCTTTAAGGTGG	10529
rs184950063	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21011825	CATCCACCCCTGGCC[A/C]CAGGGCCACACTGTT	10529
rs184951449	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20921691	CCAATAAGTGGGTTT[A/C]CTTTGTTTCCTGCTG	10529
rs184955152	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20875956	CCATCTCAGGAAAAC[C/T]TTTGTCTTTAGCAAA	10529
rs184959111	snp	C/T	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:20893030	CATTGAAAGGATTTA[C/T]CCACAACAACGTTCA	10529
rs184970255	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20977759	ACAAAAGCATCAGAA[C/T]GGTACCTTTGAAAGT	10529
rs184976104	snp	A/T	0.0119091	0.0762411	intron-variant	NEBL	GRCh38.p7	10:20789853	ATCTTATCTCAAATT[A/T]TATATATATATATAC	10529
rs184980350	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20809223	TAACTGTCAGAGAAA[A/T]TTTGAAATGTCAAAT	10529
rs184981976	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21015667	CAGGTATGCACTATC[A/G]TGCCCTAATTTTTTA	10529
rs184985201	snp	C/T	0.00835141	0.0640778	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20846359	TCCAGGTTGATTATT[C/T]ATTCATTATAGAGAT	10529
rs185000983	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21030517	AAAGGAGAATGCTTG[A/G]TGAAGTGAGGTTCTA	10529
rs185001841	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21048188	GTCTTGTTCTCCCCT[C/T]GCACGCTGTCCTCAA	10529
rs185010944	snp	C/G	0.00517822	0.0506191	intron-variant	NEBL	GRCh38.p7	10:20988709	ATAGTTATCCAGATT[C/G]ACAGCTTTGACTTCT	10529
rs185029047	snp	A/G	0.00597247	0.0543191	intron-variant	NEBL	GRCh38.p7	10:21054143	AAAAATGTGTTTCAA[A/G]TAAATTTTTTAATGA	10529
rs185040888	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21044554	GCCAAGTATTTAAAT[A/T]GGAGAGGGGTGCTTA	10529
rs185045880	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	NEBL	GRCh38.p7	10:20957966	ATATTAGTGGGTAAA[C/G]AGCCAGAATGAAACA	10529
rs185047126	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21012519	CATGAGCCACCATGC[A/C]TAGCTTATTTATTTT	10529
rs185051294	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21031045	TATGGAATGAGAACA[C/G]AGTAGTAGAAAGAAT	10529
rs185055554	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21079724	TTCCTTTATTTATTT[C/T]TCCTCCTTTGAGATG	10529
rs185069590	snp	G/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21063267	GGCCCACGTGCTCAC[G/T]TGTCATATTCATGGC	10529
rs185082484	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21042120	CAACTTCCAAAGCTC[G/T]AATGCTAAAAATTAC	10529
rs185083150	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20952679	GGAAGACGAGGTGGG[C/T]GGATCACTTGAGGAC	10529
rs185102779	snp	C/T	0.00478085	0.0486577	intron-variant	NEBL	GRCh38.p7	10:21028063	GAAACCCTGTCTCTA[C/T]TAAAAATACAAAAAT	10529
rs185111509	snp	C/T	0	0	intron-variant	NEBL	GRCh38.p7	10:21005707	CCACTGCACTTCAGC[C/T]TGGGTGACAGAGCAA	10529
rs185115164	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21060982	TTGAACTGTGCCCCC[A/G]AGAAAGATTTGTTGA	10529
rs185121912	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21081496	GGGAACTCATTTTTA[A/G]TAGTACCTATAATAG	10529
rs185128939	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20955265	GTTAAGGAGGTCAGA[C/T]ATATAGACACATAAA	10529
rs185131728	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21033932	GCATTTTGGGAGGCC[A/G]AGGCGGGTGGATTGC	10529
rs185151446	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21110710	TGGACATGGACATGA[C/G]CCCCCTGAGGCCCCA	10529
rs185157977	snp	A/G	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20886546	AAAAAGAAATTCTGG[A/G]GAAAGAAGTAAACTG	10529
rs185159106	snp	C/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21007958	TAATTCACAGATGGG[C/G]AACTTAAATTGCAAT	10529
rs185162323	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20990665	CCAAAGATATCTCAG[A/G]GAACCAACACTGTGC	10529
rs185165599	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20974712	ATTAGATGCTCAGTA[A/G]GTGTCCATCAAATGA	10529
rs185175272	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21115980	TTTTAGATAATTGCT[A/G]TATCTTCAAGTTTAC	10529
rs185201785	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20835447	CATATAGTAATCAAG[C/T]TGCTAATACGATTTG	10529
rs185208953	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21156843	ACACTAGAATCTCTA[C/T]ATTGAACTACAGCCA	10529
rs185228119	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:20992988	CGGGGTTTCACTGTG[A/T]TAGCCAGGATGGTCT	10529
rs185232849	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21103405	TTTCTCGTAGAGATG[C/G]GGTTTCACCATGTTA	10529
rs185247497	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21066803	ATTGTTCTCTTACAT[C/T]GATTTTCTTACATTG	10529
rs185251372	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21117857	AGTAGCAACTCGGCC[A/G]CTATTATCTCTATGA	10529
rs185254682	snp	C/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21062570	TGTGCACCTGTGGTC[C/T]CAGCTACACCAGATG	10529
rs185255897	snp	A/C	0.00755907	0.0610114	intron-variant	NEBL	GRCh38.p7	10:21096384	TGTTGAGGCTAGTAT[A/C]TTAGATTAGCCTGAA	10529
rs185258646	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21030873	ACGACTTAACACCTG[A/T]ACATCATGGCACTCA	10529
rs185259425	snp	A/G	0.000798403	0.0199641	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21139782	AAATATAGAAATGCC[A/G]AAGTCTATGAAAGCC	10529
rs185263464	snp	A/T	0.00597247	0.0543191	intron-variant	NEBL	GRCh38.p7	10:21154746	CTTACTCCAAATCCA[A/T]ATCTTACACAAAATC	10529
rs185271864	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	C10orf113, NEBL	GRCh38.p7	10:21148263	TTATGAAACATGTAC[A/C]TTGGTTTCCATCCAC	10529
rs185273981	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21164029	CTGTGCCCTATCTAG[G/T]TTCGACCAGAGAGGC	10529
rs185279515	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20838117	ATTATTTAAGAAATA[C/T]ATTTCATAGGGCTAT	10529
rs185290351	snp	C/T	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:21078523	CACTCCTGGTTAATA[C/T]ACTTTGGAAATCTTC	10529
rs185292298	snp	A/G			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20872342	CAGAAAAAAGCTTCC[A/G]CGCCTGATCACTTGT	10529
rs185296608	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20806250	GGGAGTAGAGGCATC[C/T]AAGCAGAGGCCCTCC	10529
rs185300125	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21108025	TGATATCCCCTTTAT[C/T]ATTTTTATTGCATCT	10529
rs185339537	snp	A/C/G	0.00358923	0.042236	intron-variant	NEBL	GRCh38.p7	10:21064254	ATTTTCTAAAAATAC[A/C/G]TACATATTTCCTTTT	10529
rs185340700	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21080329	TTGATATTGCATTCC[A/G]TGCATGAGACATATA	10529
rs185343328	snp	A/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21011984	CTTACTTTGCCTGCC[A/T]TGCTGCAGAGGCCCC	10529
rs185349182	snp	A/G	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:21108984	TCCTATTGGAATACC[A/G]TTTATTTCTTTCTCT	10529
rs185352142	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21094566	GGAGTGCCTGTAATC[A/C]CAGCTACTCGGAGGC	10529
rs185359993	snp	C/T	0.0123036	0.0774623	intron-variant	NEBL	GRCh38.p7	10:21044194	CTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC	10529
rs185366462	snp	C/T	0.00159617	0.0282053	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21127068	TTCAATACACTCAAA[C/T]GCATCCATGGTTTTA	10529
rs185378692	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20817702	TTTTACCTAAGAAGG[A/G]TAAATAAGAACTTTA	10529
rs185386223	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20879045	AATTTCGTCTCTTCA[A/G]TGTCAAAATACTGGA	10529
rs185390932	snp	A/T	0.000798403	0.0199641	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20854313	TTTTGATCTTAGGGG[A/T]TACTCCAGGGATTTC	10529
rs185392482	snp	A/G	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20788205	TCTGTGACCAGAAAC[A/G]TGAGCTATAAATGAG	10529
rs185416659	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21170667	TCCAAGAAAGTCCTG[A/C]ATTCTGTTCAATGCC	10529
rs185419915	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20790628	ACAAAACAAACAAAC[A/C]AAAAAACAAAGACAA	10529
rs185423300	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20819686	TTTTATCTTCTTGGC[A/G]ATGCCAGTCTTTTCC	10529
rs185424016	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20792523	CTGTCTAGTCCTGGC[C/T]GGGCATGGTGGCTCA	10529
rs185428162	snp	C/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20821977	ATCTAACTCCAACGT[C/T]ACCCCTTCCCCAAGG	10529
rs185429871	snp	A/G	0.00119737	0.0244387	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21130093	CAAAAGAAAGCAGGA[A/G]TAGCTATGTTAATTT	10529
rs185433332	snp	C/G	0.00716266	0.059414	intron-variant	NEBL	GRCh38.p7	10:20804317	GTACTCATTAGCGCA[C/G]TTCAAGCAGTAGCCC	10529
rs185444011	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21167775	ATAGAAATATTAGCT[A/G]TGTTTTTTGTCTAAT	10529
rs185469598	snp	A/G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20933675	GGAGGCAGAGGTTGC[A/G/T]GTGAGCCAAGATCAC	10529
rs185505046	snp	A/G/T	0.00438332	0.0466095	intron-variant	NEBL	GRCh38.p7	10:20967790	ATGGCGAATTCACAC[A/G/T]TTATCTTTTTACTAT	10529
rs185506920	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21152096	AATGAAGGAGTGAGT[G/T]CATTTCCGCTATCCG	10529
rs185508399	snp	A/G			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20876722	CACATTACTTACAAA[A/G]CTTAAAATAGAGTTT	10529
rs185524574	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20904102	AATAAAAGTTATGTG[C/T]ATGTGTTCTCTTTCT	10529
rs185531340	snp	A/C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20802044	TCCCATATCCTTTTA[A/C/T]GTTTTCCGGAGGAAA	10529
rs185531845	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21159215	TCTCACTTGAGCCAC[A/C]TTTTTTTCTTATTCC	10529
rs185538219	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20797224	TGAAGATTCATTACT[C/T]GAGTACAATGAAAGA	10529
rs185539681	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21110973	TAGGGAGCCAAATCA[C/T]GAGTGAACTCCCATT	10529
rs185544685	snp	A/C/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20780616	CCAAGAAACCACGGT[A/C/G]AGAGCCAAGAAGTGA	10529
rs185556153	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21150143	TGAAGTATGAAATAA[C/T]GAAGGCCTCACTTTT	10529
rs185560838	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20887780	CTTAGGGATCATATA[C/T]CAAATTAGAGAACAG	10529
rs185588973	snp	C/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20949256	TACAACGAGAACACA[C/G]GGACACAGGGAGGGG	10529
rs185609252	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20830003	CTATTTGTTGTTTAA[A/T]GCATTGACTTAGGAT	10529
rs185612696	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20917509	ATTTCTCAATGTATG[C/T]AAAAAGTCCGAACTA	10529
rs185617065	snp	C/T	0.00478085	0.0486577	intron-variant	NEBL	GRCh38.p7	10:20918743	ATAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG	10529
rs185632055	snp	A/G	0.00318978	0.0398085	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20873306	TCTTCTCATGACAAT[A/G]TGGTGCTCTATAAAT	10529
rs185640107	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20931965	TGTATTCCTTCCCTG[C/G]TCTTCCTCATCTAAG	10529
rs185648568	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20888325	GATTTTAAAATCTGC[A/C]GACCATTTTAATTTT	10529
rs185649570	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20799597	TGCAAATAACACTCA[A/G]ATATAGTTGGGAAGT	10529
rs185654244	snp	C/T	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20902456	TGTATATTCCCCTTT[C/T]CACAGATGTAGATCC	10529
rs185666403	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20823092	CCACTTTTAAGGAAC[C/T]GATCCTCTCGCAATG	10529
rs185673751	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21073258	AGCCCAGGAGTTTGA[A/G]GCTACAGTGAGCCAT	10529
rs185674546	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20839594	TTTCCTTTATTTAAA[G/T]AATGTGAATATAGCT	10529
rs185676130	snp	A/T	0.000798403	0.0199641	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20854932	ATGTTTTTTTAAAAA[A/T]GCCTTTTTTTGGCTA	10529
rs185691040	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21097807	AAACACGACAGGAAC[C/T]GCCCAATAAATGAAG	10529
rs185692112	snp	G/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20872841	CCGGTACCCTACATG[G/T]TCTAAAAAGGGGAGG	10529
rs185703958	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20901555	AATAAACAATTAAAA[C/T]AGATCCAAATTCAGT	10529
rs185704859	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20836276	CGCGCAGGCTGGAGT[A/G]CAGTGGCGTGATCTC	10529
rs185705921	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20945307	GTGCCTTACTCTGTA[A/C]TCCAAAAATTCCCAC	10529
rs185709380	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20819952	ATATTATTTATTGGT[A/G]GCCTCTCTGAGTTTG	10529
rs185712244	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20973016	AAAAATAAATATATT[A/G]GAAGTGTTGAAGAGT	10529
rs185715586	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20852984	AGTGGGGAAAAATAA[A/T]AGCAATTTGTCTTGC	10529
rs185722245	snp	C/T	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:20894103	AGGATATATGAAAGC[C/T]GGAAGAAGTCCAAAG	10529
rs185730618	snp	A/G	0.0103295	0.0711199	intron-variant	NEBL	GRCh38.p7	10:20916412	TTTTTGTTTTCTTTT[A/G]TTTCTTGGGAAAGGG	10529
rs185739116	snp	C/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21040285	GCAGGAGAATCGCTC[C/G]AACCCAGGAGGTGGA	10529
rs185742861	snp	C/G	0.0107246	0.0724382	intron-variant	NEBL	GRCh38.p7	10:21004521	GTCAGGAGATCGAGA[C/G]CACCCTGGCTAACAC	10529
rs185746282	snp	C/G	0.00874735	0.0655527	intron-variant	NEBL	GRCh38.p7	10:20814359	ACAGCACTTTGGAAA[C/G]CTAAGGTGGGAGGAT	10529
rs185750707	snp	C/T	0.00199481	0.0315187	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20862486	AATGGTTGCAGTGAG[C/T]CACATCACTCACCTT	10529
rs185753072	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20848223	AAGCAATGAAAAGAA[C/T]GTATAAAATACTTTA	10529
rs185765623	snp	A/G	0.00478085	0.0486577	intron-variant, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20880099	CAGGCACGGTGGCTC[A/G]TGCCTGTAATCCCAG	10529
rs185771267	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20926978	GGGGAGGAAAAATCA[C/T]TGAACAATCACAACT	10529
rs185782247	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21090533	TTCTGGAACCTACCC[C/T]CACAGATATTGAGGG	10529
rs185782725	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20783834	ATGGGGTTTTATCAC[C/T]TTAATCACGACTGGC	10529
rs185786489	snp	C/T	0.00597247	0.0543191	intron-variant	NEBL	GRCh38.p7	10:21061413	ACATGGTACATGATA[C/T]GTATCATATATTGCA	10529
rs185791804	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21076573	CATCCATGGTCATAG[C/T]AGCGTTGACCACAAC	10529
rs185795869	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21106269	CTTTGCCCATGCCTA[C/T]GTCCTGAATGGTATT	10529
rs185807067	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21169535	CCCAGCCAGTTTACA[C/T]GGCAACACGTATCCT	10529
rs185807185	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21058302	TAGATATAATCCATT[C/T]TTGCTCTTTTGGACT	10529
rs185816420	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21122743	AGAAGAGATATCTAT[C/T]TGAGTCACCAGTAGA	10529
rs185820177	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21002458	TATTTTATTACAGAA[A/C]TAAATTCTTAAATTA	10529
rs185823135	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20897601	CAGCTCTAACACTCA[A/G]GATAGCACAGTCCAA	10529
rs185838228	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20987492	CACTTATGCAATGCA[C/T]TCCACATCCTCACTC	10529
rs185848424	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20934316	GAAGGGATATATAAA[G/T]TGTTTGGGACTATTT	10529
rs185849030	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20930925	AATCGACATCTGCTG[C/T]GTGGACAGTCACAGC	10529
rs185849663	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20869063	GGGAAATTTTCTGGG[G/T]AATTGAGACCCTGTA	10529
rs185850297	snp	A/C	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20914620	TATATATTTCTTTTA[A/C]AACTCCATTTATATT	10529
rs185853654	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21042488	AGCAAAGGTAATAAA[C/T]GTTCAAATCTCTTCA	10529
rs185855778	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21085505	CCAAGCATAGTGGTG[C/T]ACACCGATGGTCCCA	10529
rs185867636	snp	G/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21025134	CATGAGAAATGGATG[G/T]TCAAAGAGAATCAGG	10529
rs185873503	snp	A/G	0.000314016	0.0125263	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20869731	TCAAGGTTTAGAAAG[A/G]GAAGTTACATTGCTT	10529
rs185875622	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20985137	ACATAAAGTGTACAA[C/T]AAATGTAATGTACTT	10529
rs185878761	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20969750	AGGGTTTTGCCATGT[A/T]GCCAGGCTGGTCTCA	10529
rs185879163	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20884926	ATAGCTAATAAAATG[A/G]CCTCCTAAAAACTCT	10529
rs185885583	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20919715	TGCAGAATATGAAAC[C/T]GTGGAACAAAACATA	10529
rs185886037	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20962842	AATATGATTGTTAGT[A/G]TAGTGTAGTCTTCTG	10529
rs185888010	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20950223	CTCCTAGCAATGTGC[A/G]CGGCACATAGTAAAC	10529
rs185890347	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20897894	TAGTATTATACTGGC[A/G]AGTATGGTATTGTAT	10529
rs185895634	snp	G/T	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20942266	ATGGAACAGAACAGA[G/T]CCCTCAGAAATAATG	10529
rs185900416	snp	G/T	0.00953873	0.0683987	intron-variant	NEBL	GRCh38.p7	10:20932629	AATAAGTATTCTTGC[G/T]GAAAACTGCTACACA	10529
rs185920828	snp	C/G	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:20985712	TCCCACAATCTACTA[C/G]TATGCAGCTATACTG	10529
rs185923819	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20982480	TAATATCACTAAAAT[G/T]GTATTTAAAACAATT	10529
rs185935066	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20917792	CTATTTTATATTTCA[C/T]TTTCAAGATACTTCT	10529
rs185936807	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21056057	TAGAGTAGAGTGAAA[C/T]AGAAAGAGCAACTAG	10529
rs185941867	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20945950	AGTTTGCTCATCAGT[A/G]AAATGAGAATAATGA	10529
rs185945616	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21023226	TCTACAATGATTAAT[C/T]TGAAAATTTTACATA	10529
rs185946192	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20884670	TGTGCTGTTAACCCC[A/G]TAGCATAGACACCTC	10529
rs185959207	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20914285	ACAGGCTAAGAAAAC[A/G]TGTATTTGGAGAAAA	10529
rs185965176	snp	A/G	0.00119737	0.0244387	intron-variant, downstream-variant-500B	NEBL	GRCh38.p7	10:20815565	AAGCAAAGGAGGACC[A/G]CAAGTAAATAATAAA	10529
rs185973320	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20799958	GTGTGTGAGACGGAG[A/C]AAGAGAGAGCGCACG	10529
rs185977663	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20830894	GGGTGAAAGAGTGAG[A/T]CCTCCATCTCTAAAA	10529
rs185980543	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20852862	TCAGCATATGAAACA[C/T]GCAAGAGAGGCAGAG	10529
rs185993546	snp	C/T	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:21072120	ACCGTGCCTGGCCCA[C/T]TGGTTTTTTTTTCAG	10529
rs185994865	snp	A/C	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20784773	ATTTACTAGAGTATA[A/C]ATGTTATTTCCTAAG	10529
rs186000466	snp	C/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21090215	AAGAACCACTGCCTA[C/G]TAAAACTACACACAA	10529
rs186015633	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20939845	GACAAAGAAGGCCAT[C/T]ACATAATGGTAAAGG	10529
rs186019283	snp	G/T	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:20963557	TCATAGGTATTTTTG[G/T]TTTTTTCTTTTTGTT	10529
rs186031866	snp	C/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21034934	CCCAGCATGCACTAG[C/T]TATTTATTCTTATTT	10529
rs186035483	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21002744	CAACCAGATCTCGGG[A/G]GAACTCACTTACCAT	10529
rs186047993	snp	A/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20998326	GAGAACAATCATGCT[A/T]ACCTAAGAAAGGTAT	10529
rs186048638	snp	A/T			upstream-variant-2KB, intron-variant	C10orf113, NEBL	GRCh38.p7	10:21148376	ACTTTGGTCCGTGGT[A/T]CCCAAAGCAGCTTTG	10529
rs186051165	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21016859	ATAGATACCTACCCA[C/T]GTTTTTGCAAAAATG	10529
rs186054517	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21165638	CCCAATCTCGTCTAC[A/G]TGCCAGGCTTGGGGG	10529
rs186055571	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20971022	ATTAGTTAATTTATT[A/G]TCTGTAACGGATCCT	10529
rs186057524	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20999133	TTTACCATACAAAAA[C/T]TGTACAGAAACCCAG	10529
rs186078593	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21094434	GTGAACCACAGAGGC[A/G]GAGCTTGCAGTGAGC	10529
rs186084669	snp	A/C	0.0185938	0.0946107	intron-variant	NEBL	GRCh38.p7	10:21039149	CCAATGGGTTACTTG[A/C]ATAAATTTTCTCCCA	10529
rs186091282	snp	A/G	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:20810349	AATTGAGAAGTTTAT[A/G]TTTAAAAAACAAAAC	10529
rs186093655	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21055506	ATGAAAACCCACCCA[C/T]CTGTTTTGCTACTTT	10529
rs186096222	snp	C/T	0.00119737	0.0244387	downstream-variant-500B	NEBL	GRCh38.p7	10:20779903	ATTTCAAATACAGTG[C/T]GCTTGATTCATAATA	10529
rs186098676	snp	A/G	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:21049764	TCTTTGCAGGCAAAG[A/G]CTGTGTTTCTGCATC	10529
rs186108454	snp	G/T	0.0130921	0.0798413	intron-variant	NEBL	GRCh38.p7	10:21071749	TAAAACAACAGAAAT[G/T]TATTCTTTTGCAGTT	10529
rs186108643	snp	A/C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20994616	AAAATCTGCATATAA[A/C/T]ATTTGGTCCCCCAAA	10529
rs186108983	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21122461	TCTCCTCCATACTTG[C/G]TTTGCATATTTAGGC	10529
rs186110438	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21038415	TCCTCCCTGTGTCCA[C/T]GTGTTCTCATTGTTC	10529
rs186112735	snp	G/T	0.00438332	0.0466095	intron-variant	NEBL	GRCh38.p7	10:21014145	AATATTATTTTAGAT[G/T]TAGGGTCTCACTCTG	10529
rs186122286	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21085393	TTGGGAAGCCGAGGC[A/G]GAAGGACTGCTTGAA	10529
rs186129554	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21158711	ATTTCCTTAATCCAA[C/T]GCAAAACGACTTGAT	10529
rs186134760	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:21117726	ACGCATCTCTCTATA[C/G]CTAAAAAGCTTCCAC	10529
rs186143097	snp	G/T	0.0166325	0.0896639	intron-variant	NEBL	GRCh38.p7	10:21103290	GCAATCTCGGCCCAC[G/T]GCAAGCTCCGCCTTC	10529
rs186145517	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20982097	ACTTAACACAGCTGT[G/T]TGTGATCAACGTTCA	10529
rs186153904	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20923138	CAGTGGTGCCATCAC[A/G]GCTCACTGCAGCCTT	10529
rs186177310	snp	C/T	0.00119737	0.0244387	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21140640	ATAACAAGACATTTA[C/T]GGTAAAATAAAATCA	10529
rs186177880	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21022772	CATACAAGATGATTA[C/T]GCTTGTATAACCGCT	10529
rs186180825	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21016631	AAAGATTTCAGAATT[C/T]GAAAACTTGGAGCTA	10529
rs186183742	snp	C/T	0.00438332	0.0466095	upstream-variant-2KB	NEBL	GRCh38.p7	10:21176005	ATCTTTTTTTTTTTT[C/T]CTGAGACAGGGTCTA	10529
rs186190475	snp	A/G	0.00398564	0.0444627	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20884340	CCTCGGCCTTCCAAA[A/G]TTCTGGGATTACAGG	10529
rs186190890	snp	C/T	0.00318978	0.0398085	intron-variant, upstream-variant-2KB	NEBL, LOC102725112	GRCh38.p7	10:20843870	CTTATTAAAAACATC[C/T]AATCAATTATAGTTA	10529
rs186194588	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20859037	CCTTTAAGTATATTT[C/G]ATCTCTATTTCTAAG	10529
rs186194700	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20897284	AGTGCCCTTGAGATG[C/T]TGACGTCTCTGGTGC	10529
rs186198926	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20877925	CTCTTTCTTTTGCCT[A/G]GTAAACCTCCACTCC	10529
rs186213356	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20812416	CACGTTGGTGTGCTG[C/T]ACCCTTAACTCGTCA	10529
rs186230587	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20828133	ATAAAAATATAGAAG[C/T]TTAGAAATTTATTAA	10529
rs186231888	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20796553	CAACTGCTTTTTCTC[C/T]AGAAAAAATTAGTCT	10529
rs186234608	snp	A/G	0.00835141	0.0640778	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20782028	AAATCCCAAATCTAA[A/G]GTTAATGTTTATATA	10529
rs186242065	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21106041	TGGGGTTGTTTGTTT[G/T]TTTTCTGGTAAATTT	10529
rs186244834	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20798176	AGATCAGGCAGTAAT[A/G]AGTAGCAAATCTCGC	10529
rs186248240	snp	C/T	0.00119737	0.0244387	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21143995	TATTCGAATAAGATA[C/T]CACTGAAAACTCCAA	10529
rs186270561	snp	A/T	0.0023933	0.0345097	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20864023	ACTACTAAATTTTCA[A/T]GGCAATTTATAATGT	10529
rs186275321	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20911319	GCATGAACAAACTTA[A/G]AATAAGATCTTCTAT	10529
rs186280813	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20849215	AAGAAGGAAAACACA[C/T]ACACATACACACACA	10529
rs186295706	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21119519	TATAGTTATATTGAG[C/T]AATATACTGAATATA	10529
rs186320822	snp	C/G	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:21068202	CAAATGTGTTGAACA[C/G]TTTTATAAAGTTAAA	10529
rs186324008	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21035605	CTGCTGTGTTCAGTG[C/T]CTTGAATCAGGAGAA	10529
rs186326621	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20793659	CCCAGGCTCAAGCGA[C/T]CCTCCCACCACAGCC	10529
rs186327836	snp	C/T	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:21105789	AATGGTTGAACTAAT[C/T]TATACTCCCACCAAC	10529
rs186332014	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21050593	TAAAGCAAAATAAAG[A/G]AAGTGAGGAACGGGT	10529
rs186333793	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21155115	GAGGGAGGAGAATTG[C/T]TTGAACCCAGGAGGC	10529
rs186342964	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21083392	ACCCCAGTAGCAGCA[A/C]CCCACCTCCTTGTAG	10529
rs186344993	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21121777	TTGACAGTAGCACAT[C/T]AGACAGCCTGGAGAT	10529
rs186352589	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21157613	GAATTTGTTTTATAA[A/G]ATTCTTCAGTTCACT	10529
rs186356061	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21100250	TGTGTGGTACCCGAC[C/T]ATTCCCCACCATCAG	10529
rs186366881	snp	G/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20890819	AGTATAATCACACTG[G/T]CACACTAATTGCTGC	10529
rs186374292	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20827422	AGCTTACTCTGAGAG[C/G]TGGCGCTTGCCAACT	10529
rs186386703	snp	C/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20974572	TAATTTAAATAAAAA[C/T]ATATCATTATTTTTC	10529
rs186389335	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20804470	TGGCCTCTAGCTGTA[A/G]CATGATTTATTTCAA	10529
rs186427067	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20894910	CTCCAGCCTGGGTGA[C/T]AGAGCGAGACTCTGT	10529
rs186435685	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20945502	TTAATAACATCATGC[A/G]TCACGTGAATAAACC	10529
rs186437962	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20955056	TCAGATGTGCATTTT[A/G]GGAAAACCTTGCAAG	10529
rs186438146	snp	A/G	0.00318978	0.0398085	intron-variant, downstream-variant-500B	NEBL, LOC102725112	GRCh38.p7	10:20880576	CTTGTACAAAGCAAA[A/G]TTCCAATGCCTGAAA	10529
rs186439770	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20894430	GTGAGCTGCAGTCAC[A/G]TGACAGAACTCCAGC	10529
rs186449245	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20910544	CCTCACTGCATGAAC[A/C]ATGGTCAGAGAGACA	10529
rs186454254	snp	G/T	0.0150606	0.0854603	intron-variant	NEBL	GRCh38.p7	10:20922770	ACTCGAGCCATCCCA[G/T]CCCTTCCGTTGCTCC	10529
rs186458258	snp	C/T	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:20838826	CACTTGCTGAAGGAT[C/T]AGATGATCATTAGCA	10529
rs186461863	snp	C/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20864510	ATAAAAGGTGAGAAT[C/T]CTGCCCATTCACTCT	10529
rs186476502	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20979509	CTCGTATAATTCTCA[C/G]AAGAGATCTAATATT	10529
rs186476978	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	NEBL, NEBL-AS1	GRCh38.p7	10:21175382	CGGAAGAGTCAGCTA[A/G]GATTATTATAAATTG	10529
rs186479721	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20792786	GCCTAGGTGACAAGA[A/G]CAAAATAATTCTGTC	10529
rs186493225	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20806882	ATCAATTCCAGTATG[A/C]TGAACTGAGTAACAT	10529
rs186493532	snp	A/G	0.0138799	0.0821421	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20853630	CCAGTTCTACAAAAA[A/G]TAAAGAAATCAGCTG	10529
rs186494363	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21044702	TGGTCAACATCTATG[C/T]ACCCTTTATCACCCT	10529
rs186503345	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21013744	TTAGCTAGGCGTAGT[G/T]GTGCGCACCTATAAT	10529
rs186519613	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20942588	GCCAAAATTGGCAAA[C/T]GGGACCTAATTAAAC	10529
rs186524057	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20820624	TGAGGTCATGAGTTC[A/G]AGACCAGCCTGACCA	10529
rs186531660	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20805106	GCCAATGAACTAGAC[A/G]TGGGGTATGAGTGAA	10529
rs186538828	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21016981	CCTTTACATACATTG[C/T]ATCAACCCTTGTATT	10529
rs186541666	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20837266	ACAGTGCTACCCCAG[A/T]GAACACATGAATTAT	10529
rs186544025	snp	A/C	0.00636936	0.0560724	intron-variant	NEBL	GRCh38.p7	10:20807589	AATTACACAATTATA[A/C]AATCTTTCGCAGCTT	10529
rs186545161	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20953920	GCATAACCGATCTTG[C/T]ATTGAAGGGGTAGAC	10529
rs186546432	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20859409	GGTAACTACTGTCCT[A/G]ACCACTAATTTGTGT	10529
rs186547831	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20878300	GGAAACATAAAAAAG[C/T]TAGGCAAAGATGTTG	10529
rs186551168	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20999335	GATGCAGTGGCTCAC[A/G]CCTGTAATCTCAGCA	10529
rs186567076	snp	C/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20791653	TCTTGTCTCAGACTC[C/G]CAAAGCACTGGGATT	10529
rs186572135	snp	G/T	0.0119091	0.0762411	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20877498	AGTCTTTTTCTTTTC[G/T]AACAAAGAGCAGCCT	10529
rs186595036	snp	A/G	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:20810900	ATTTAAGTTTCATAC[A/G]TATTATCCTCATTTT	10529
rs186597368	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20873887	TGGTATATTCCTCCA[C/T]TTCTTCGAATATTTT	10529
rs186599369	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20843114	TGATTAGGGTTAGAT[A/G]GGATTGTGAGAGTGG	10529
rs186630243	snp	C/T	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:20922266	CTCTCTGTGTCATAG[C/T]GACCCAAATATAGGC	10529
rs186636116	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20807821	TAGTCTTAACCTTTA[A/G]AAACAGATTTATAAG	10529
rs186647072	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20840056	ACCCTAGTTTGAGTT[A/G]GGTTTCTGTCATTTG	10529
rs186664958	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20994319	TCCATATAAGAGAAG[C/T]TAGAGGCAAAGTACA	10529
rs186676309	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21112680	CAACAAACATGGCAC[A/G]TGTATACCTATATAA	10529
rs186684955	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21151705	ATTGCTTTTCCCACA[C/T]GCCCCAGGTTCACTC	10529
rs186693421	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21065065	CAATAATGAGGCATC[A/G]TGACCTTTTACTGAA	10529
rs186696332	snp	A/C			intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20959614	AATAAATTCACCAGA[A/C]CTCAGAGCACTTAAC	10529
rs186698118	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21031236	GAGGATGATGATGAA[C/T]CCTATGGGGGTCACC	10529
rs186707699	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21033022	TAATACACACACACA[C/T]ACACCTACATATTGT	10529
rs186717780	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21046762	CCTGCCACCACGCCC[A/G]ACTAATTTTTTTTAT	10529
rs186719274	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20889501	TATCTCTGATATATC[C/T]ATTAGGAAACAAAAT	10529
rs186721668	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21095761	TGCAATGAGATGTAA[G/T]ATATTCCCTTCAGCT	10529
rs186728236	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20948540	TAGTTATGGAAGTGT[C/T]TACAATAAAGGCACA	10529
rs186731252	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21080745	CTGTTTGAGTAAATG[C/T]AACTTTGATGGAATG	10529
rs186732278	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20903706	AAGAACAAAATAACG[A/T]ATTTTGTAGCAACTG	10529
rs186735515	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20933375	CCTCAAAACTTACCC[A/G]TACACTACTAGACTA	10529
rs186738072	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20918265	CAGGAGGCTGAGGCA[A/G]GAGAATCGCTTGAAC	10529
rs186741536	snp	A/G	0.00874735	0.0655527	intron-variant	NEBL	GRCh38.p7	10:20905461	AGCCAGCAAGAGCAG[A/G]GAAAACTGCCTTATA	10529
rs186745860	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21082832	CAGTGGCATATTCTC[A/G]GCTCACTGCAACCTC	10529
rs186750550	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20980540	ATATAGCGTGCATGG[G/T]ACAAACAGTGCAGGT	10529
rs186751521	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20928189	ATACTTGGTACAGTT[A/G]AAAAAGTAGATTCAC	10529
rs186752698	snp	A/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21050081	AAGGTCCTTTTCATC[A/T]CTAAGTTCTAGATAA	10529
rs186765687	snp	G/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21032397	ATTCTTCTGGGATTT[G/T]GGGGTCTAAGATGCT	10529
rs186770902	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21014403	ATCTGACATGCAATC[A/G]GTATCCAGTGGCAAA	10529
rs186775858	snp	C/T	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:20987716	TAAGACCAAGGCTAA[C/T]TTCTGCATGGTGAGG	10529
rs186777971	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20973343	CCTCCAATCTCCTAA[A/G]CTCAAGCAATCCTCC	10529
rs186780937	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21064692	TACAAGCCATGTTTT[C/T]ACCATATCAAAATGA	10529
rs186786308	snp	A/G	0.0425829	0.139564	intron-variant	NEBL	GRCh38.p7	10:20938795	ACGTGACGAATGCAC[A/G]AGCCTCAGTAGCCGA	10529
rs186792810	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20995087	GGTTGGAGAAAACAC[A/G]GAGGGCATGGGGACC	10529
rs186799568	snp	A/G	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:20977267	CTGACCTAAAGTTAA[A/G]AGAGAAAGAAAGTGA	10529
rs186804014	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20970546	AGCTACTCAGGAGGC[C/T]TCTGAGGTGTGAGGA	10529
rs186819696	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21010676	GTATACAAATATATA[A/G]AGTTACTCTACTTCT	10529
rs186822196	snp	A/G	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:21030428	ACACTCAGTAAGGAG[A/G]AAGACTGTCACTCTC	10529
rs186830137	snp	G/T	0.0240643	0.107019	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20855166	ACCTGGGAGCGGAGG[G/T]TGCAGTGAGCTGAGA	10529
rs186833672	snp	C/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20992009	CATTTCTTTACACAA[C/T]CCACCACTGAAACGA	10529
rs186838215	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20909520	TGTACCCAAATAGAG[A/C]CTGCCTTTTCTACAT	10529
rs186839789	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20935014	ACACGATTTTATTTA[C/T]TCGTTAAAACACTTA	10529
rs186844336	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20888874	GGAGAATGGAACATA[C/G]CTAAGACAAACAAAC	10529
rs186847758	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21002543	TATAAAGAACTGAGA[C/T]GGGGTAATTTATAAA	10529
rs186851083	snp	C/G	0.000135142	0.00821905	intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20823300	CTTCTTTGTATTTCA[C/G]CTGCATAATTTATAA	10529
rs186870429	snp	A/C	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:21039578	ACGACAAGAAGATTC[A/C]AGAGAGAACTAAATT	10529
rs186872962	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21099744	CTGTGAGCCAGGAAA[C/T]GAGGGTATTTCCAAC	10529
rs186882557	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21056902	ATGCAGTACAGCTAA[C/T]CCCTTTCTTAAGCTC	10529
rs186884171	snp	A/G	0.0391387	0.134304	intron-variant	NEBL	GRCh38.p7	10:21023610	TGAGGCAGGAGAATC[A/G]CTGGAACCCAGGAGG	10529
rs186897515	snp	C/T	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21132061	CTCAAAGTTATGCAA[C/T]AATAACCATTATATA	10529
rs186920671	snp	A/T	0.000798403	0.0199641	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20855955	ATTTTTTACATTAAA[A/T]TGTTAAAGTAGGCTA	10529
rs186929120	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21035223	GGCTGTTTTCAAACT[A/C]CTGGCCTCAAGTGAT	10529
rs186935829	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:21094880	GGAGAGACTAGAACC[C/G]TCTCGTCATAGTTTC	10529
rs186936837	snp	A/G			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20875419	TCCTTAAATAGTTCT[A/G]GGTTAGACATGGCCA	10529
rs186940233	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21061809	ATGACTGCTTGGCAG[A/G]GGTTTCTCCCCTGCA	10529
rs186942167	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21083932	TCCAGAGGCAGCGTA[C/T]CTTTTCTTACTGAAG	10529
rs186943793	snp	A/G	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:21153671	CAGATGCACACCACC[A/G]CAACCAGCTAATTTT	10529
rs186944026	snp	A/T	0.0225045	0.103662	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21127747	ATAAAGGGAATTAAA[A/T]GGGGGAAAGGAGTGG	10529
rs186945443	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21067789	CAAGACCAGCCTGGG[C/T]AACATAATGAGAACT	10529
rs186948860	snp	A/G	0.0162398	0.0886349	intron-variant	NEBL	GRCh38.p7	10:21077500	TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG	10529
rs186955451	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21043548	ATTTTGTGCATACAG[A/G]CACACATACATGATT	10529
rs186955473	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21100587	TTCTGTTAATACAGG[A/G]CTTGGGGAGGAAAGT	10529
rs186964368	snp	A/T	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21134930	TCCGTTTGTGGTCTA[A/T]GTACACACATCACAC	10529
rs186967936	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21114333	ATTAAGATTTGTTTT[A/G]TGGCCCAAAATATGG	10529
rs186987600	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21081264	CTAAGCTGGCCTAAA[A/G]TCAATGGGGCCACCA	10529
rs186992090	snp	G/T	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21134297	AGACTACAGTTGAAT[G/T]AAGTCATGTCCTACT	10529
rs186996055	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21110657	CATCCATCTTCTCTC[C/T]TACCTAAGCATATGC	10529
rs186998339	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21170456	CAATTATCCCGTTTA[C/T]GGGTGCTTGGGGCCC	10529
rs187001966	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21096269	TTGATTCCCTGCCTT[C/T]CCCTATTCTCATCCT	10529
rs187002206	snp	C/T	0.000798403	0.0199641	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21129065	TGCTAAATTATCCTT[C/T]AGAAGTGAGGGAGAA	10529
rs187010358	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21080587	TATACATAAATCATT[A/G]TAATAAAAATAATTT	10529
rs187013714	snp	A/G	0.00517822	0.0506191	intron-variant	NEBL	GRCh38.p7	10:21046072	AAAGAAGAAAATCCC[A/G]TCATTTGTGACAACA	10529
rs187020059	snp	C/T	0	0	intron-variant	NEBL	GRCh38.p7	10:21149666	ACTCTAGCAAATTAA[C/T]AGAATCCAAGGACAG	10529
rs187032223	snp	A/T	0.00438332	0.0466095	intron-variant	NEBL	GRCh38.p7	10:20950819	ATTCTATCAAAAATG[A/T]CAGTGTTAAGAATAA	10529
rs187042063	snp	C/G	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:21074776	AGCCACTGCACCTGG[C/G]CATATAGATATATAT	10529
rs187064113	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20985380	GTCAAGGAAACCTCC[G/T]TTACCCACTCACAAA	10529
rs187095205	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20794162	GCCACGAGGCGAGGG[A/G]AAGCGGACCCCATTT	10529
rs187105603	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20952254	CCAGCCTGGCCAACA[C/T]GGTAAAACCCCGTCT	10529
rs187108746	snp	C/T	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:20906302	ATCAAGTTACTAACA[C/T]CTATGTTCACTGAGG	10529
rs187110517	snp	C/T	0.00636936	0.0560724	intron-variant	NEBL	GRCh38.p7	10:20937760	ACAGCACTTTTCCGA[C/T]GGTTTTAGCAAACGG	10529
rs187116971	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20801587	GTTCACCTAACAGAA[C/T]GTGAGCTCTCTAAAA	10529
rs187119566	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21167054	AGCACTGGCCTCGAT[A/G]ATCACACTCAACAGG	10529
rs187125699	snp	A/C	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21138625	TTTAAAAAAACTATA[A/C]TCCAGGTGCTATGTT	10529
rs187126245	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20787474	AGTGATCTCTAGATT[A/C]GTAGAAATCTTAGTA	10529
rs187127788	snp	A/G	0.00795532	0.062565	intron-variant	NEBL	GRCh38.p7	10:20816890	CCTAGACTTTGCCCA[A/G]AAATGGAGTCATGAT	10529
rs187141808	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20886202	ATTTTTTTTAATAAG[A/G]TTATCTAGGTATCTC	10529
rs187143334	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20985983	CCCTTTAGGTTAAGG[A/G]GATTTGATCTACTCT	10529
rs187144865	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21003995	TCAAATGTGTATCAC[A/G]GCTAAAAATTCTGGT	10529
rs187146135	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21109364	TGACTTGATCGTGGC[A/G]GATAAGCTTTTTGAT	10529
rs187148188	snp	A/G	0.00716266	0.059414	intron-variant	NEBL	GRCh38.p7	10:20900828	CCAGCCTAGGTGACA[A/G]AGTGAGACTCCATCC	10529
rs187152578	snp	G/T			upstream-variant-2KB, nc-transcript-variant	NEBL, NEBL-AS1	GRCh38.p7	10:21174484	TTCTCTTCCCCAGCC[G/T]GGGGCACCCTCATCC	10529
rs187152864	snp	C/G	0.0119091	0.0762411	intron-variant	NEBL	GRCh38.p7	10:20915740	TGTGTCTTTATAGCA[C/G]CATGATTTATAGTCC	10529
rs187155764	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:20930570	ATGGCCCTGCCTAGT[C/G]TCTCCTACTAAATCC	10529
rs187155786	snp	C/T	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:20971460	TTCTTTTTTTTTTTA[C/T]TATACTTTAAGTTTT	10529
rs187171760	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20790464	AAAATTAGCTGGGCG[C/T]GGGGTGTGTGCCTGT	10529
rs187176447	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:21109497	AGGTTTTGGTGTCAG[C/G]ATGATGCTGGCCTCA	10529
rs187178980	snp	A/G	0.00119737	0.0244387	intron-variant, nc-transcript-variant	NEBL	GRCh38.p7	10:20819021	ACTTTTTCATGTTAT[A/G]ATGATATGATTCATC	10529
rs187179910	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20798973	CAAGTTTCGCTGCCC[A/G]AAACTTTTTCTTAGG	10529
rs187185988	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20782933	AGGATCCCTATACAG[A/C]TTTGTTTTCAGAACC	10529
rs187192569	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	NEBL	GRCh38.p7	10:20813711	AGTTTACAGTAGTCA[C/T]GTTAGAAATAAAGAC	10529
rs187204166	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21151910	TTTACTGATTGTTTG[A/G]TTTTGGGTTTTGTCT	10529
rs187209967	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20800242	TTCTTTCTATGTCTG[G/T]CTTATTTCACTTAGT	10529
rs187217734	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20831061	AATCAAGTTTGGCCA[A/G]TGGTTTCTTAGTGAA	10529
rs187230861	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20854554	ACATGAAAATGTTCA[C/T]ATAGTACTTTTTTTT	10529
rs187250571	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21089993	TGTTGATGACTCCCC[A/G]GTTTGTATTTCCAGC	10529
rs187252395	snp	A/G	0.0111196	0.0737302	intron-variant	NEBL	GRCh38.p7	10:21124684	AAGGCCGAGCATAGT[A/G]GGTCATAGCTGGAAT	10529
rs187254692	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	C10orf113, NEBL	GRCh38.p7	10:21147023	CAAGATTTCTGAAGG[A/G]CCTGAGGCTTCTAGT	10529
rs187257783	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21162487	TTGATGCTAACTCCA[C/T]ATGGTTGGCATCAGA	10529
rs187262422	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21113610	GAACTTTCCTTACCA[G/T]GTTTGATAAATGTTG	10529
rs187271643	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20890971	CTGAAAAAGTGTTCC[C/T]GTTTCAGATGATAAA	10529
rs187286262	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20920054	AGTGTAAGAGAGGAC[A/G]CCCAAGCTTCTTACT	10529
rs187288189	snp	A/T	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:21036316	CAAATTAGCCAGGCG[A/T]GCTGGTGTACACCTC	10529
rs187295888	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21018407	TCCAGATTCTGGTAC[C/T]CCTGGGGGTGTGAAT	10529
rs187322062	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21006924	AAGGCACAGGTGTTG[G/T]GTGGGGAAAGAAAAA	10529
rs187325719	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20949173	CTGGCCAGAACTTCC[A/G]TTCTCAGCAAACTAA	10529
rs187326703	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20946703	CACCGCGCCAGTCCC[A/G]TTTTATTATTCTTTA	10529
rs187345806	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20834987	TGAATGAACATGGTC[A/G]TTCAGGTTATATCAG	10529
rs187348418	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21041850	TTCCTCCCCACTTTA[C/G]ACCATATATAGTAAT	10529
rs187350462	snp	C/T	0.0107246	0.0724382	intron-variant	NEBL	GRCh38.p7	10:20911426	AATGGCTGAAACCCA[C/T]ATTTTAAAACTCTCT	10529
rs187355791	snp	A/C	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:21000405	GGATTCTGGTCCCCC[A/C]ATTAGTCCCCTGTCA	10529
rs187360555	snp	A/C	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20983673	GGTGTGTCCAGGGAC[A/C]GAACCCAAAACTTGG	10529
rs187361685	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20967623	ACAGAGCGAGACTCC[A/G]TCTCAAAAAAAAAAA	10529
rs187362350	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20982692	ATCACTTAGCATACC[A/G]TAGGTATTCAAAAGT	10529
rs187365299	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20867826	TTTATCATATATTAA[A/G]TTCTTATACATACTG	10529
rs187370381	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20803338	TGATCACTATATGGT[A/G]TATATATCGAAACAT	10529
rs187378944	snp	A/C	0.000798403	0.0199641	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20865780	TTTATAAGTGAAAGT[A/C]CCTTGTTAACTGTAA	10529
rs187379809	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20882110	CTGATCCCAGGAGGT[C/T]GAGGCTGCAGTGAGC	10529
rs187386216	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20848600	GGCATTAGATTCTCA[C/T]AGAAGCACAAACCCT	10529
rs187387064	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20894943	AAAAAAAAAAAAAAA[A/T]AAAAAAATTAAGGCA	10529
rs187392346	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20832209	GATCTGCTGGACTCA[A/G]TAAATCATTATACCC	10529
rs187401438	snp	C/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21040230	AATTAGCTGGGTATG[C/G]TGGCGGGTGCCTGTA	10529
rs187408840	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20850250	ACAAGATCCCAGGCA[G/T]TGGGTGGCTGGGTCT	10529
rs187423602	snp	A/G	0.00028172	0.0118651	intron-variant, downstream-variant-500B	NEBL	GRCh38.p7	10:20817549	TCCCTTCATTCACAC[A/G]TGGACAATGCATTTG	10529
rs187427531	snp	C/T	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:20801874	TAGGGTGGGTTAAAC[C/T]GCTACAAAATTCAGA	10529
rs187433373	snp	A/C	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20900275	TATGGCTAAACTCTC[A/C]AAGTCCAGGTCTGGC	10529
rs187433713	snp	A/G			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21134230	GACTCCATCTCAAGA[A/G]AAAAAAAAAAAATCT	10529
rs187438028	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20816735	TTCTTGAACTGCATC[C/T]GTGAATTATTTCAAC	10529
rs187452158	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20930076	TTTATGCCTCTTCTC[C/T]GCCTTCTCCCCTGAG	10529
rs187462729	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20786319	ATGTACTTTTCTTAA[G/T]TTGATGCTAAAAATG	10529
rs187466308	snp	C/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20871251	CATCATTTAGGGGTA[C/T]TTATTAAAGATTTAG	10529
rs187485423	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	NEBL, LOC102725112	GRCh38.p7	10:20844574	TAGTTTTAAGGTCTT[A/G]ATATTAAGAAAATTT	10529
rs187495385	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21072819	AACATGATAAAACTC[C/T]GTCTCTACTAAAAAT	10529
rs187514835	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21058076	TGCAATCAGCTCAGC[A/G]TGTTTTCTCAGAAAT	10529
rs187516757	snp	A/G	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:21086570	ATCACTTGAGCTCAG[A/G]AATTTGAGACCAGCC	10529
rs187517104	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20813221	GAGCTTGTAAAAATA[C/T]ATATTCTCAAATCCT	10529
rs187521574	snp	A/G/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21025239	AATATGACATGTAAC[A/G/T]CATTCAGAGCTGGTT	10529
rs187526045	snp	A/G	0.00993419	0.0697739	intron-variant	NEBL	GRCh38.p7	10:21104447	GTAGAAGTTTTACAC[A/G]TTTTTCCTCAAATTT	10529
rs187532086	snp	A/G	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21140895	GCAAACCACCATGGC[A/G]CATGTATACCTAGGT	10529
rs187536486	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21120167	CTTGAGACCAGAATT[C/T]GAAACCAGCCTGGCC	10529
rs187548788	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21052972	TGACTATAGTCACAA[C/T]AATATATTGTCTATT	10529
rs187549668	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21109757	CCAGGAATTCATCCA[A/T]TTCTTGTAGATTATC	10529
rs187550353	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21122909	CCAGTGAATACTCTC[A/G]TCTTCCTAAGTTCTG	10529
rs187553572	snp	A/G	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:21084979	AGTGGGTTAGTGCGG[A/G]AAAATGTGAAAGGGT	10529
rs187555206	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21070151	TACTTGAGTTGGAAT[A/T]TGGCCAGGACACTGG	10529
rs187555321	snp	C/T	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:21058488	AGGAAAGAAAAAGAA[C/T]AAGTTGAAAACCTAT	10529
rs187557592	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20929103	TTGATCCAGCAATCC[C/T]GCTACTGGGTATCTA	10529
rs187559820	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21116230	TTAAACAACAGATAT[C/T]TATTTCTTACCATTC	10529
rs187565693	snp	A/G	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21144865	TGTAAAATAGTGGTT[A/G]GCATGGGCTCTCTCC	10529
rs187567066	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21101890	TCAGTTTAGGAAACA[C/T]CACGCTTTGACTAGC	10529
rs187567506	snp	A/G	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21137699	GCACTTTGGGAGGCT[A/G]AAGCAGAAGGATTGC	10529
rs187570527	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21161690	TCTATTGACTGACTG[A/G]GGATGGTGGATTTTA	10529
rs187583303	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20980033	GTGAATATATTCTTT[C/T]AAAGTGTCTCATTTC	10529
rs187584001	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20899115	TATTTTATTTGTTCC[A/G]TAAAAGGAAAGAATG	10529
rs187587154	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20965508	CCTTTAGAAAGGTCA[A/G]GGAAGGCCGCTCTGT	10529
rs187589467	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20879048	TTCGTCTCTTCAGTG[C/T]CAAAATACTGGAAAC	10529
rs187590708	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20915082	TGCTGAGATTACAGA[C/T]ATAAGCCACCATGCC	10529
rs187591986	snp	A/C	0.00636936	0.0560724	intron-variant	NEBL	GRCh38.p7	10:20989277	ACATATTTAATCCAA[A/C]TTTACTTTGGGGAGG	10529
rs187595533	snp	A/G			intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20960679	CATATTTATATATAA[A/G]TGCATATATAATATA	10529
rs187596719	snp	A/G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20892845	AAAGTATCTGGAAAG[A/G/T]CTCTTCACAAGTGAA	10529
rs187597460	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20999586	CATGGGCAACAGAGT[A/G]AGACCCTGTCTCACC	10529
rs187601509	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20943304	GGGACATGGATGAAG[C/T]TGGAAACCCATCATT	10529
rs187610548	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21060568	CCCTCTACTGGCTCA[C/T]ATATTTTAAAATGGT	10529
rs187614210	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21027404	AGGATCACACATCAC[C/T]GCAGCCTCGACCTCC	10529
rs187621537	snp	C/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21167347	CCATAATTAAAGATA[C/T]ATTTGACTAAGATAC	10529
rs187632207	snp	A/G	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21036784	ACCATCCGCCTGAGC[A/G]TGGACATACCCTGTC	10529
rs187632819	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21035841	ACATGTACATACATA[C/G]AGAGACAGGAAGAAA	10529
rs187663799	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:20966560	TTTCTGCCAAAGTGT[G/T]CACCCTTAGTGACAG	10529
rs187685462	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20782561	GAAAAACCAGATCTG[C/T]ATCTTCTTCAAGAAA	10529
rs187689989	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21161961	CTCAGTGCACCAGAA[A/G]AACCAACTCTGTGAT	10529
rs187727672	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20885685	GGAAAAGTTACCTTC[C/T]CAAGGAAGTATAAAA	10529
rs187741622	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21068687	TTTCTGCTCTAGGTA[C/G]TTGGTGTTGAGTTTC	10529
rs187755075	snp	A/T	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:20798677	ATGCTAGAGCCACAT[A/T]TATGTTCTTCCTGAA	10529
rs187765402	snp	C/G	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:20991399	GACAATCAATTTAGT[C/G]ACATTTATTATCATA	10529
rs187765873	snp	A/G	0.00597247	0.0543191	intron-variant	NEBL	GRCh38.p7	10:21092073	TACAGAGTATCAGCA[A/G]CTACAGGCAATCTGA	10529
rs187771338	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20840573	CATCACATAGAAAGG[A/G]GATTTTAAAAAAAAT	10529
rs187775262	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20824345	CATAAAGAAACAGTA[C/T]CTAAATATCTCAGAT	10529
rs187777806	snp	A/C	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21040399	AACTGCACAGGGTGC[A/C]TGGCACCAGCATCTG	10529
rs187791699	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21004685	AGATTGCACCACTGC[A/C]CTCCAGCCTGGGGCA	10529
rs187798020	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20794412	GTATATACTATATCC[C/T]GCTTACTGCTGACCA	10529
rs187806028	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20829623	GAAAGGTAACTACTA[C/T]TCATGTTGAAATGCA	10529
rs187813167	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21073337	CAAAAAAAAAAAAAG[C/T]CAGACACGGTGGCTC	10529
rs187815558	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20860499	ACTATATTTTTCTCC[A/G]TGTATAGAGAAATAT	10529
rs187815737	snp	C/G	0.00279162	0.0372561	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20845717	CAAGGTGAGTGGATC[C/G]ACTGACTGGGGGAAA	10529
rs187828251	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21120389	CAAAAAAAAAAAAAA[A/C]ATACATATATATATA	10529
rs187832244	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20814196	GTTCTAGAATAGCAA[A/C]CTAAAATTTTACAAT	10529
rs187835415	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20943618	GTTGAAAGAGCCTTA[C/T]GAATTTATCACATAA	10529
rs187838503	snp	C/T	0.000798403	0.0199641	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21141781	AATCTTTCCTCTGCC[C/T]TGAACCCAAAATTGA	10529
rs187838592	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21156238	CAGGAGAGTTTTCCA[C/T]TTGGCATCTTTTTGG	10529
rs187843363	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21015483	ATGATATTAAAATAA[C/T]CAGTAAATTTATTTT	10529
rs187844341	snp	A/G	0.00716266	0.059414	intron-variant	NEBL	GRCh38.p7	10:20799192	GCAGAGTCTTGCTCC[A/G]TCACCCAGGCTGGAG	10529
rs187856031	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20981020	ATCTCAAACTCCTGG[C/T]CCCAAGCGATCCTAC	10529
rs187858233	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21047918	ACTTTGCCAAGAAGA[C/T]CACTTTCACCCTACA	10529
rs187863951	snp	G/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21072394	CTTACTCCAAAGAGG[G/T]TCACATTCTGAGGTT	10529
rs187875270	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21017470	TCCCACAGATCTTTG[C/G]ACATCTCGCCATTAG	10529
rs187875288	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:20957386	TTGGTATACTTTTTT[A/T]AAAGTGTCACTCTTA	10529
rs187879491	snp	C/T	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:20983309	ATTTATAATAATCAC[C/T]AAATACACATAAAAT	10529
rs187895945	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21051081	GAAACCCAGCCAGGA[C/T]GAAAAAAGAAGAAAT	10529
rs187915414	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20795015	TTTAATGCCAAAAAT[A/C]TGACTTCAGAACCCA	10529
rs187920133	snp	C/T	0.0111196	0.0737302	intron-variant	NEBL	GRCh38.p7	10:20825558	TGTAATCCCAGCTAC[C/T]CGGGAGGCTGAGACA	10529
rs187942199	snp	G/T	0.00279162	0.0372561	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20855327	AGTTATCTTGTAATA[G/T]GTATTTATAAAATAA	10529
rs187946488	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20875074	AAATCTGTTCTTTGT[C/T]GCTTCCAACGAATAT	10529
rs187946888	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20925128	AGGCTCCTTTTGTAG[A/G]GACAAAGTCACTGTT	10529
rs187976257	snp	C/T	3.45596e-05	0.00415676	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21146337	GCCCCCAACACATAC[C/T]CTACCTGTTCATGTC	10529
rs188001338	snp	A/G	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20924546	AAAAAAAATCCCAGC[A/G]GGTAGCTAAGCACCA	10529
rs188022702	snp	C/T	0.00716266	0.059414	intron-variant	NEBL	GRCh38.p7	10:20912127	AAATATGAATGTAAA[C/T]GTAAAAACATGAAAA	10529
rs188029769	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20976554	ACTGAAGAAAGAAAA[C/G]GTGCTACATATACAC	10529
rs188031581	snp	A/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20956270	GCGGTTGTTCAGAGG[A/T]TCTAATTAAACAGGG	10529
rs188032634	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21115529	TTGTATGGAAGTCTA[A/G]GTGAGAGTTTTTTTT	10529
rs188049291	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21152299	CCCCAAGGACAGTGA[C/T]GCCAGTGTAATATTT	10529
rs188062174	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21106925	TAAGTTAAATTCCTC[A/G]GTGTTTTATTCTCTT	10529
rs188064844	snp	A/C	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20895238	GTTAGCTCAGCTATA[A/C]TTGCACTTCAATAAA	10529
rs188085465	snp	A/G	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:21034692	AGGAAACTGTCTAAC[A/G]CACTTCAATTTATTA	10529
rs188089485	snp	C/T	0.00438332	0.0466095	intron-variant	NEBL	GRCh38.p7	10:21048927	GGCAGGGAGAATTGC[C/T]TGAACCCGGGAGGTG	10529
rs188093204	snp	A/G	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:20839469	CCATGATTTCCTTTT[A/G]GGAAATGACCTCTAA	10529
rs188097257	snp	A/G	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:20822574	AGACTATATAGAGAT[A/G]TATACAGACTATCTA	10529
rs188097341	snp	A/G	0.00557542	0.0525036	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20879290	GTTTTCATGAGAATC[A/G]GAAATGATCAAAGTC	10529
rs188101415	snp	G/T	0.00716266	0.059414	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20854596	TTTGGACAGGGTCTT[G/T]CTCTGTCACCCAGGC	10529
rs188103643	snp	A/G	0.00438332	0.0466095	intron-variant	NEBL	GRCh38.p7	10:21016110	TCATGCTATTTCTTT[A/G]AAGCAGTTCATGCTG	10529
rs188108258	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20920631	ATAAAGACAAACAAA[A/G]ACTAATAAAAAGAAG	10529
rs188109449	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20893231	TGACTCCCCATCAGA[A/G]GACTACTAGATCCAG	10529
rs188117249	snp	C/G	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:20793041	TTTTTTAATCTGAAA[C/G]GATTCTTAGCACTAC	10529
rs188118814	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20944414	TCATAATAAAATAAA[A/G]TAAATTATATAAATA	10529
rs188119765	snp	G/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20995687	CACATCAAAACATCC[G/T]TGAATTCCTTTTTAA	10529
rs188135664	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20806964	TCTCTTTAAATATCA[A/G]TATTATTCTGCATCT	10529
rs188138682	snp	A/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20891717	ATTAAAAAGATACAC[A/T]TATTTGTATATTTTA	10529
rs188150636	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21066242	AATTTCCTCTTCCAC[A/G]TACTTTTACAGACCC	10529
rs188154699	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21033698	TGAGTCAAGATTGCA[C/T]CACTGCACTCCAGCC	10529
rs188159015	snp	A/G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21086157	ATTTTCACAATTTCC[A/G/T]TAGGAATTAAAGAGT	10529
rs188174800	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20860343	GTCCTGGGTCAACTT[A/C]ATGTCAATGTAAAAC	10529
rs188179686	snp	G/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20876069	GTCTAGGCATGCTGT[G/T]CATAAAAACCTACTA	10529
rs188190061	snp	A/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20808874	GCTCTTTTAAGTCTC[A/T]ATTTTAAAGGACGGG	10529
rs188191600	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20904009	CCCCCAAAAACCATC[A/G]AAATAAAAATAAATT	10529
rs188200025	snp	G/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20841966	TTACATACAACTTAT[G/T]TTTCTCTGCTAATGA	10529
rs188215190	snp	C/G	0.0111196	0.0737302	intron-variant	NEBL	GRCh38.p7	10:20923578	CAGCTACTCAGGAGG[C/G]TGAGTCAGGAGAATC	10529
rs188236549	snp	A/G	0.0236746	0.106192	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20851603	ATATAGTGAAACCCC[A/G]TCTTTACTAAAAATA	10529
rs188248204	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20921714	TCCTGCTGCACCTTA[A/G]TATGTGACAACACAC	10529
rs188255145	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21102731	GTTGGAATTCTGGAT[G/T]GTTTGTAGTTTAGAG	10529
rs188257456	snp	C/T	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:20787828	TTGTTCGGTAGTTAA[C/T]AAAAAGTCCATACCC	10529
rs188265263	snp	C/T	0.0119091	0.0762411	intron-variant	NEBL	GRCh38.p7	10:21094491	TGGGAGACAGCGAGA[C/T]TCCGTCTCAAAAAAA	10529
rs188266786	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20872930	ACCAGCAGCCTTCGG[G/T]GCTGCTCTGTCTACG	10529
rs188268758	snp	A/G	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:20908030	AGCCATGAAGTCTTC[A/G]AAGTTCTTGAACTCT	10529
rs188269218	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21063555	AATCAACAGTGGTTA[G/T]ATTTTTCTTCTGATT	10529
rs188269417	snp	A/G	0.00279162	0.0372561	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21138195	ATTGGGACAACGGAC[A/G]GCACTGTCCCAACTC	10529
rs188274997	snp	A/C	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21080224	TAGATACAACAAAAG[A/C]ATGTCATCACTTTCT	10529
rs188275045	snp	G/T	0.00874735	0.0655527	intron-variant	NEBL	GRCh38.p7	10:21116662	TTCTTTGAATGCCTG[G/T]TAATTTCTTTTTCTT	10529
rs188278486	snp	G/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21108834	GGCTTTACGAATCTG[G/T]GTGCTCCTGTATTGG	10529
rs188282858	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20952712	GAATTTGAGGCCAGC[C/T]TGGTCAATATGGCGA	10529
rs188285335	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21152950	TTATGTACTTAGAAC[A/C]AAAGTCTTGGTCTCC	10529
rs188285854	snp	A/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21051233	TTATATTCGGAGATC[A/T]CATTTTTTATTGTAA	10529
rs188289321	snp	A/G			intron-variant, upstream-variant-2KB	NEBL, NEBL-AS1	GRCh38.p7	10:21172993	CCGGGATGACTGTCA[A/G]GATGGCAGCTTGTTC	10529
rs188290993	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20791054	GTTTGACAGGTTGTT[C/T]TATGTCAACAAGATT	10529
rs188292350	snp	C/T	0.00636936	0.0560724	intron-variant	NEBL	GRCh38.p7	10:20933902	TTAAGAAGCCATTTC[C/T]TTATCACCAACTATT	10529
rs188310779	snp	A/G	0.00517822	0.0506191	intron-variant	NEBL	GRCh38.p7	10:20905286	CAAGTGTATTAGCCC[A/G]TTTTCACATTGCTAT	10529
rs188321032	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20919525	TGAAACATTAACCGA[C/T]AGAATGAGATAAACA	10529
rs188327840	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21084617	AAAAATAAAAAAATA[A/C]AAATAAAAAACAGCA	10529
rs188328377	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21031062	GTAGTAGAAAGAATG[A/G]ACAATTCTCTCTGTT	10529
rs188329056	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20949793	TAAATGGCTGTTAAG[C/T]GATTTAGATGGTTTG	10529
rs188329867	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20991049	CTGACATTTGACAGC[A/T]TTTCTCTACAGGGAC	10529
rs188332517	snp	A/T	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:21044592	AGAAAATAAATTCAC[A/T]TGGCTGTTCACAGAT	10529
rs188332989	snp	A/C/T			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21136757	TTCTCCTTCCCAAAC[A/C/T]AGCAAATATTTTATT	10529
rs188340365	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21013309	ACCTTGAAAATAAAC[A/G]TGCTGAAGCTTCTCC	10529
rs188341577	snp	A/C	0.000798403	0.0199641	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20877440	ATAGTGAGGGTAAGG[A/C]AGTCCTTCGTAAGAC	10529
rs188346984	snp	C/T	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:21171467	GTGGAGAAACATATG[C/T]CCCTGGGCAGCAAGG	10529
rs188348444	snp	G/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20955683	TTAGTGGGTCATAAT[G/T]AGGGTCTTGATGAAA	10529
rs188349793	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20890551	ATCCTCCTCCTGAGC[A/G]CAGAGAAGAACTGAA	10529
rs188358702	snp	A/G	0.00438332	0.0466095	intron-variant	NEBL	GRCh38.p7	10:21028274	AGAAGAAGAAGAAGA[A/G]GAATGAGAAATAAAA	10529
rs188390329	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20962093	AGACTACTTGATGCA[C/T]GAATCTGGCTGACAG	10529
rs188394028	snp	A/G	0.0352966	0.128072	intron-variant	NEBL	GRCh38.p7	10:20972704	GTGAGCCAAGATCAC[A/G]CCACTGCACTCCAGC	10529
rs188416640	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21004299	ATAAAAAAATAAAAA[A/T]TCAAAGCCATTGAAA	10529
rs188419474	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20878777	GTATAAGTAAACACA[A/G]CCTTCTCCCATAAGT	10529
rs188433091	snp	C/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20907066	GTGGTGACCATGTTG[C/G]ACAGTATAGCTCTAT	10529
rs188443850	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NEBL, LOC102725112	GRCh38.p7	10:20845434	TGAAAAGAGATTTGA[A/C]CAAGAGTTCCCAGAA	10529
rs188448292	snp	C/T	0.00874735	0.0655527	intron-variant	NEBL	GRCh38.p7	10:20818042	GAAGTCCATTCCCTG[C/T]CACCCTAGAAGGCTT	10529
rs188457806	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20937827	GGTCCTACACCCATG[A/G]AGCCTCGCTCATTGC	10529
rs188460306	snp	G/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20802966	TTAAGCCTAATAAGG[G/T]TAAATGACCCCTTTG	10529
rs188469690	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20834323	ACAATGACTATCTCT[C/T]AGGACGAGAACAGAA	10529
rs188474823	snp	A/G	0.00636936	0.0560724	intron-variant	NEBL	GRCh38.p7	10:20907450	CTGATACATACTTAT[A/G]TGACTGAATAATAAA	10529
rs188475304	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20889663	TGAAGCATACATAGT[A/G]AAATCTGTCAATCTA	10529
rs188476937	snp	C/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21155296	CAATCCAATTATATT[C/T]TATTAGTTATTTTTA	10529
rs188480643	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21058901	ATTAGGTTTGGCTCC[C/T]ACTAATTGTGTAAAG	10529
rs188491149	snp	A/G	0.0528381	0.153711	intron-variant	NEBL	GRCh38.p7	10:20940098	ACTTAATAGACATCT[A/G]CAGAACTCTCCACCC	10529
rs188492135	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20789797	GGTCAAGGCTGCCAT[A/G]TGATCTCACCACTAC	10529
rs188494939	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21073778	AGGAGATGAATGCTA[C/T]GAAATGCCTACTATA	10529
rs188495973	snp	A/T	0.0130921	0.0798413	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21129793	CATATAAAATGCACA[A/T]TTAAAACCGTAAAAA	10529
rs188497052	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21040729	AATCTCATGTCAAAT[C/T]GTAATCCCCAATGTT	10529
rs188501623	snp	A/G	0.00636936	0.0560724	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20856634	GGAATAGAGGAATGT[A/G]AAAAGAGGTGTGGGA	10529
rs188504618	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21098615	AAATTCCTCCCTTCC[C/T]AATCAATCCATGAAG	10529
rs188512798	snp	A/G	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21131667	CCTCTGGTGTGTATG[A/G]CAGGTCATGACATAG	10529
rs188518563	snp	C/T	0.00914312	0.0669923	intron-variant	NEBL	GRCh38.p7	10:21112231	TTGACCCAGTGATCC[C/T]ATTACTGGGTATATA	10529
rs188522654	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21150941	TCGATGCTCAAAAGA[A/G]GTGAGAGGAATGTTT	10529
rs188529864	snp	C/G	0.000313503	0.0125161	intron-variant	NEBL	GRCh38.p7	10:20826439	AATTAATGCTGTAGA[C/G]AACTTACTGAACTAA	10529
rs188531492	snp	C/T	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:20973652	CTCTTTCTCTTCACG[C/T]AGACTTTGTCAAGAG	10529
rs188539302	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21168501	TTCATAACAGCTAAA[G/T]GTAAAGTATGAGCGC	10529
rs188543696	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20953442	GAGAAAAATTTCTGT[C/G]GCTTTACGCTGCCCA	10529
rs188566270	snp	C/T	0.0107246	0.0724382	intron-variant	NEBL	GRCh38.p7	10:21025921	TTATAATATTATTAT[C/T]ACTATTACTATTAAT	10529
rs188567808	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21096826	GTGTATATCTTTTTA[A/G]CATAGATTTTGGCTA	10529
rs188573008	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20963675	GCTGGGATTGCAGGT[A/G]TCAGCCACCACCACA	10529
rs188576440	snp	A/G	0.00557542	0.0525036	intron-variant	NEBL	GRCh38.p7	10:20988278	ACTTGTCCTGAGTCC[A/G]TGACTTTCCCATTCC	10529
rs188581092	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21106760	GGATAGTATTGAATG[A/T]ATAAATTACCTTGGG	10529
rs188598419	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21101456	CCCCTTCTTGTTAGA[C/G]GGAAAGTGGACATGA	10529
rs188603116	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21069614	ATTGAAGCATTCTGC[A/C]CTTTGGAGCATTTAA	10529
rs188627038	snp	C/T	0.0111196	0.0737302	intron-variant	NEBL	GRCh38.p7	10:20975499	TCAGCACCATCAATA[C/T]ATCAGTAGCAAGAGC	10529
rs188637125	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20918389	GCTCCACTGTTCACC[A/G]AGTTTGTGAGTTTGG	10529
rs188647240	snp	A/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21009742	ATTTCTTGAGCCTGT[A/T]TTTATCCTTTTGCAA	10529
rs188665700	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21042873	CAGAGAGCCTTTGCT[G/T]TCACTTAAAGAATTA	10529
rs188669661	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21076824	CAAATTCATAGAGAC[A/G]GAAACTAGGCAAAGG	10529
rs188672365	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20987243	TTCTAACCAAACCCT[A/G]AGTGGGTATTTCCTA	10529
rs188682263	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20952334	CCCAGCTACTAGGGA[A/G]GCTGAGGCAGGAGAA	10529
rs188689463	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	NEBL, LOC102725112	GRCh38.p7	10:20885157	TTCATCCAATACTCC[A/G]AGTTAGGACATCACA	10529
rs188696153	snp	A/G	0.00517822	0.0506191	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20853788	GAGTGCAAAAATACC[A/G]TTAGAGAGAATGAGT	10529
rs188698000	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20814940	TAAATGCTGATTCTC[A/G]GGCAAACAGCTATTC	10529
rs188700271	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20837740	ACAAGCTGACTCTTA[C/T]TAGGGTCTAACACAG	10529
rs188703604	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20820411	AGTAGAGCTGGAGGT[G/T]AAGATCTCATTAGAA	10529
rs188705387	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21024654	AAATTACAATATCTG[G/T]AGGAACCTAATTAAT	10529
rs188707337	snp	C/T	0.0023933	0.0345097	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20872287	ATATTAAGATTGACA[C/T]GAACTGCAAATTCAA	10529
rs188716703	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20921296	ATTTGCCTCCGGCCC[A/C]GCTCCATTATTCCTC	10529
rs188717658	snp	A/C/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20830552	GAAAACCTCACTGTT[A/C/G]CCTTAATTTTTACCT	10529
rs188718227	snp	A/G			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20853450	AAGAAAATGTGGCAC[A/G]TATACACAACGGAAT	10529
rs188720432	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20784212	TCATAGCTGTGAAGT[C/G]AGACCCTAAGTGAAT	10529
rs188732915	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20799860	CAACATGATGGTATG[C/G]GATACATATACGTGG	10529
rs188733574	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21077729	TTTCCCTTCTTCATT[C/T]TCTGTCCTCCCTTCC	10529
rs188734294	snp	A/G	0.0119091	0.0762411	intron-variant, upstream-variant-2KB	NEBL, NEBL-AS1	GRCh38.p7	10:21172777	ACGATTTCTGAGCTC[A/G]GTTAATGAAGAAACG	10529
rs188737739	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21107497	ATATGTTGAATCAGC[C/T]TTGCATCCCAGGGAT	10529
rs188739455	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21037988	TAAGACATACCCTAG[A/G]GAGATTTCAGAATCA	10529
rs188743000	snp	C/T	0.00398564	0.0444627	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20852478	ACGCACGGCAGTGAG[C/T]GGCGGGCCTCAGGAT	10529
rs188747715	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21054494	TCTCGGACAGGCATC[A/G]GGGAATTGTTTTTGT	10529
rs188749020	snp	C/T	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:20791567	TGCCCAGCTGATTTT[C/T]TTTTTTCCCTACAGA	10529
rs188749597	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21093057	TTGTACAATTTATTG[C/T]ATTTTATTTTTGTTC	10529
rs188759380	snp	A/G			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20867422	GCAACTTGAGAAATG[A/G]GTATTTTCAAAGTCA	10529
rs188763805	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20883750	TGGGTTATCACAGAA[A/G]TGATGAGTCAGCAAG	10529
rs188771284	snp	A/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21110887	AAAGTAACACTGCCA[A/T]CTTTGAAAATGTCTG	10529
rs188781818	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21150039	ACTTAAGTTATGTTC[C/T]TTTTTTAGCATATTA	10529
rs188786668	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20834653	TCTCAGGATACTCCA[A/C]TGAAGCCCCCACCTA	10529
rs188791997	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20802066	CGGAGGAAAACAGAA[A/G]CACATAGCATACCTG	10529
rs188792492	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20818462	GCCTTGTTAACTATT[C/T]TTGCTTTATTCACAA	10529
rs188831768	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21081769	AGTAAGGATGTACCC[A/G]AAGAATGATGGAATT	10529
rs188833826	snp	A/G	0.0130921	0.0798413	intron-variant	NEBL	GRCh38.p7	10:21148767	CTGACCTTAAGTGAT[A/G]CACCCGCCTCAGCCT	10529
rs188836000	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21087762	TTGCAGCCCTGACCT[C/T]GGTATAATTGAGATT	10529
rs188863732	snp	G/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21091506	AAAATACTTCACTTC[G/T]TTATCCAATTAGCTA	10529
rs188908260	snp	G/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21028940	CCACTAAAAAATAGC[G/T]ATACTAATATGAGAC	10529
rs188920374	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20897037	TAGAAGACCTATTTG[A/G]AAAAAAAGAAAAGAA	10529
rs188927573	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20913399	TTCTGTTTCTTAATA[A/T]TTCTCAAAAACCAGA	10529
rs188927940	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20866445	ACATTATTCCTATTA[C/T]GTTCTCTAAGCAATG	10529
rs188928706	snp	C/T	0.00478085	0.0486577	intron-variant	NEBL	GRCh38.p7	10:20795864	ATTTAGTTGAAAATA[C/T]AATTAATTCCATGAG	10529
rs188935977	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20925750	AAGCTATCAAGAGTA[C/T]ACAATTTGGAGTAGA	10529
rs188941623	snp	C/G	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:20918007	AAATGATATATGCAT[C/G]ACACAATGAAAATAG	10529
rs188944721	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20944914	AAGAGGCCACAAGAT[A/C]CCATATGACAATTAG	10529
rs188953962	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21061543	TATTACATCATATAT[A/T]TTATACATATATAAA	10529
rs188955670	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20930666	ACTGCAGAACTTTCC[C/T]ACTTGCTACCCCTTC	10529
rs188964199	snp	A/C/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20996505	CCAACCTCACAATAA[A/C/T]CTTTTGGGAGAGATA	10529
rs188965732	snp	C/T	0.00438332	0.0466095	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20870783	CTCCTTCTGAATGCA[C/T]GTTAGACACAAACCA	10529
rs188966283	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20894181	TCTCATCTACAGAAA[C/T]GAAGCAGGGCCAGCC	10529
rs188970291	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20889287	TCTAAATGCTCTCAG[A/G]AAGAAACTACATAAT	10529
rs188970328	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20833766	GTCTCAAAAAAAAAA[A/G]AAAAGAAAAAAAGAA	10529
rs188976785	snp	A/C	0.00795532	0.062565	intron-variant	NEBL	GRCh38.p7	10:20981419	ATAAAAAAAACACAC[A/C]CAAAATTATAAAACA	10529
rs188978496	snp	A/C	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20909525	CCAAATAGAGCCTGC[A/C]TTTTCTACATAGCTG	10529
rs188983014	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20962302	ATTGACAGCTAGCCC[C/T]GTCCAAGAAGTTTTT	10529
rs188986764	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20970322	CATTTAGGAGCTCCT[C/T]CAGTCCTTTTTGGAT	10529
rs188991134	snp	C/T	0.00716266	0.059414	intron-variant	NEBL	GRCh38.p7	10:20950231	AATGTGCGCGGCACA[C/T]AGTAAACACTTTAAA	10529
rs188996167	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20783174	GTTGTTCAGGCATGT[A/C]ATTTTTTTTTAAATG	10529
rs189001015	snp	G/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21022463	ACGGAGTCAGATTCG[G/T]GGTAGGAAAATGTAC	10529
rs189003345	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20836641	AGCCACAGAAGTTCC[A/G]GCAGTTTGCAAGAGG	10529
rs189003897	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20863701	CTAATCTGTTTTCCC[A/G]TAATAGTGGATCAAA	10529
rs189005720	snp	A/G	0.00279162	0.0372561	intron-variant, downstream-variant-500B	NEBL, LOC102725112	GRCh38.p7	10:20880219	TACAAAAATTAGGCC[A/G]GTGTGGTGGTGGGCA	10529
rs189006812	snp	C/T	0.00438332	0.0466095	intron-variant	NEBL	GRCh38.p7	10:21062491	CATAGAGAAACCCTG[C/T]CTCTACAAAAAAAAT	10529
rs189007439	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21152388	TTCCCAAAGTTATAC[A/G]ATGCCCCTGGGCTAT	10529
rs189009829	snp	C/T	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:20916351	GCTAGAGTTCTATTA[C/T]GAAATATTTCTTAGA	10529
rs189010788	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20814465	AAAAAAAAAAATTAG[C/T]TGGGCGTGTGCCTGT	10529
rs189012695	snp	A/G	0.00835141	0.0640778	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20846514	GGAGAGAAACAAAGG[A/G]TGTTCTGAAAGTCTA	10529
rs189016496	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20985212	TCTTCCACAAAATTG[C/G]TCCCTGGTGCCAAAA	10529
rs189017550	snp	C/G/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20804804	GATATGGGTCTTGTA[C/G/T]GCAATGATGAAAATT	10529
rs189018682	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21002522	ATTAGTCCATTCTCA[C/T]GCTGCTATAAAGAAC	10529
rs189032412	snp	A/G	0.00517822	0.0506191	intron-variant	NEBL	GRCh38.p7	10:21163432	TCTGCACTGAGGTAT[A/G]CGTTTGCTGCAGTGT	10529
rs189044813	snp	C/G			utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20783863	GCCATTTCAGTGAGA[C/G]AAAACCAGCCAAACC	10529
rs189055949	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:20788398	GTTTTTATAATAAAA[G/T]AAATAAGATTTAATT	10529
rs189081836	snp	A/C	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20997948	TTTACTACATAACTT[A/C]ATTAAAAGTATTAAA	10529
rs189099290	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21015809	TAAGCCACAGCACCC[A/G]GCTAGAAATTTCTTT	10529
rs189103307	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21034457	ATCCAACATTCTTCT[C/G]AGCACAGTAACGCAG	10529
rs189104547	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21104879	TGTAGATGCCCGATA[C/T]CAGGATGAAGAAGTT	10529
rs189112148	snp	A/T	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21128387	GAAGAGGCTCTCCAG[A/T]CCAAAAATGTCACAC	10529
rs189130082	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21165953	TATCTTTCAATCACC[A/G]CTTCCAATAAAAAAT	10529
rs189158289	snp	A/C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20931173	CTAACCAAAATTTCA[A/C/T]TGGGAAGATGTTATC	10529
rs189168978	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21089913	TGCCTTCTTTTAAAT[C/T]TAAAAATGATTACAC	10529
rs189169316	snp	C/T	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:20901771	TTGATGACCGTCTTC[C/T]GGAAGGTTCCTGCTT	10529
rs189179707	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21074688	TTTCACTGTGTTAGC[C/T]AGGATGATCTTGATC	10529
rs189180482	snp	G/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20933169	GATTTGAAGCCTTTA[G/T]ATTACTTATGGTTCA	10529
rs189183837	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21105539	TTTTATGGCTGTATA[A/G]TATTCCGTGGTGCAT	10529
rs189185243	snp	A/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	NEBL	GRCh38.p7	10:20958847	TCACCCACTCTCACC[A/T]CGTTCATCACACTCA	10529
rs189193565	snp	G/T	0.0150606	0.0854603	intron-variant	NEBL	GRCh38.p7	10:20942124	AAAAAAGAGCCCACC[G/T]TGCCAAGTCAATCCT	10529
rs189200062	snp	A/G	0.00119737	0.0244387	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21143005	GTGTGTGGGGTGTGT[A/G]TGTGTGTGGGTATGT	10529
rs189200628	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20926783	AATAAGCTTTGCTAA[C/G]AGTATTCAGGAGAAA	10529
rs189202077	snp	C/G	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:21121614	TCAAGTTAGAAAATC[C/G]TAATCTTAGAATGAG	10529
rs189213209	snp	A/G	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:21012281	CTCTCTGGGGCCACA[A/G]GTGTGAAGCAGGATG	10529
rs189214144	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20902953	GAGTGTTCCCTTCAG[A/G]ACTATACTGTTCTTT	10529
rs189214809	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20993275	AAGGACATTACCACA[C/T]TGCAGGCAAAAGATA	10529
rs189215822	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21156917	CAAGAACTATGTCAT[C/T]TTCTATAAAAATTTA	10529
rs189218489	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20978862	GGAGTATGTCTCCAT[A/G]TCTACCCCTAGAAAG	10529
rs189226808	snp	A/G	0.00279162	0.0372561	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20882590	ACAGATGAATAAATG[A/G]GTTTACTAAACATTC	10529
rs189228177	snp	C/T	0.00755907	0.0610114	intron-variant	NEBL	GRCh38.p7	10:21018871	TGTCCCTACTAAAAA[C/T]ACAAAAATTAGCCGG	10529
rs189232367	snp	A/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20912596	TCCAGTATAAGTCTT[A/T]ATCTCTTGCCGGCCT	10529
rs189240470	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20817746	TGGGCTCCACTGAAA[C/T]ACCACAAAGGACAAG	10529
rs189246067	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20827239	TTGGTAATCCAGTGG[C/T]CCCCGCGTGGGTGGG	10529
rs189249465	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21060082	CTAGGGTTTAATGCC[C/T]GGTCATCTAAAAAAT	10529
rs189250286	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20850991	TTTTTCATAGACACT[A/G]AGTAAAACACTCACA	10529
rs189260836	snp	A/C/T	0.00597247	0.0543191	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20860836	AATATTTTAGGCATG[A/C/T]ATAGGGTGATGGTCT	10529
rs189269864	snp	A/G	0.00199481	0.0315187	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20883275	ATTCAGTCCTGCCCA[A/G]CCATGTTCCTACCTC	10529
rs189287687	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20830008	TGTTGTTTAATGCAT[G/T]GACTTAGGATTTTAG	10529
rs189318680	snp	C/G	0.00119737	0.0244387	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21126582	AAAAGGAATCATAAA[C/G]ACCAACTAACCCAAT	10529
rs189328481	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20799601	AATAACACTCAAATA[C/T]AGTTGGGAAGTACAA	10529
rs189334512	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21037417	AAAATCAAGTTAGAT[C/T]AATAAAGTAAGAACA	10529
rs189336836	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21001386	AACACAGCCAGAGTT[C/T]TTCCTATCAGAAAGA	10529
rs189351469	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21070510	CTAAATCATGCTGTT[C/T]TAAAGAGTACATAAT	10529
rs189362999	snp	A/G	0.0103295	0.0711199	intron-variant	NEBL	GRCh38.p7	10:20981815	GTTGTCACAGAAGAC[A/G]TGAATTGAGAGATAG	10529
rs189376750	snp	A/G	0.0103295	0.0711199	intron-variant	NEBL	GRCh38.p7	10:20792525	GTCTAGTCCTGGCCG[A/G]GCATGGTGGCTCACG	10529
rs189392663	snp	A/G	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:21067240	CCTCCCAAAGTGCTG[A/G]GATTACAGGTGTGAG	10529
rs189392769	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21082182	AAAGTCACCAAGCAA[C/T]GAAGGAACTCTTGCA	10529
rs189394062	snp	C/T	0.00199529	0.0315338	intron-variant	NEBL	GRCh38.p7	10:21016851	CCATTAGGATAGATA[C/T]CTACCCACGTTTTTG	10529
rs189397422	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21111474	TTGATAAACCTGACA[A/G]AAACAAGCAATGGGG	10529
rs189409086	snp	C/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20916448	CTCTGTTGCCCAGAC[C/T]GGAGTGCAGGTGCAG	10529
rs189412125	snp	G/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21082383	TGTGGTTATGTAAGA[G/T]AATGCCTTGTTTGTG	10529
rs189414103	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21049991	CCAAAGTGAACATGA[A/C]AGGTTACTGAAGAGC	10529
rs189416207	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21105150	ATAACTTTTACATAC[A/G]TGTTCATGAAGAATA	10529
rs189437817	snp	G/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	NEBL	GRCh38.p7	10:20945375	ATTGACGGCTGTGCT[G/T]AGATCTTGTACCCTC	10529
rs189440246	snp	C/T	0.000462336	0.0151972	intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20888099	AGAAAAACCCTACCT[C/T]ACTCTGGAGCTGTGT	10529
rs189442938	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20913751	ACCCTGCATTCTTGG[A/G]TTAAATACTATTTGC	10529
rs189444395	snp	C/T	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21138944	CAAAAGTAAATAGCA[C/T]ATCGTAATAAATAAC	10529
rs189446328	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21163142	CTGGAGAGAAGGAGG[C/T]TAAATGGAAGTGGAT	10529
rs189450423	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21117797	TCAGTTGAGTATAGC[A/G]TGGTGGTTATAAAAC	10529
rs189456430	snp	A/C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21154527	TCATGACTTTGTGCT[A/C/T]GTGGGTCTCAATAAC	10529
rs189457100	snp	C/T	0.00557542	0.0525036	intron-variant	NEBL	GRCh38.p7	10:20982172	CGGGTACTCAAAAAT[C/T]ATTTGCATATGGTTT	10529
rs189484999	snp	C/T	0.0134861	0.0810011	intron-variant	NEBL	GRCh38.p7	10:20984742	CCAACCCCCAGGCCA[C/T]GGACTGGTACCGGTC	10529
rs189488776	snp	G/T	0.00795532	0.062565	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21143386	CCCGGGACGTGGAGG[G/T]TGCAGAGAGCTGAGA	10529
rs189491633	snp	A/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20796785	GTAACTATAATTCAA[A/T]CCACAAATATAAGCA	10529
rs189496604	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21157798	TATTTGGAGATAGGG[C/T]CTTTGCTGAGGTAAT	10529
rs189511629	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20896192	TACCCTTTCTCTGGA[C/T]CAGCAATCCTCTTAG	10529
rs189520923	snp	G/T	0.00119737	0.0244387	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21142561	AAATGAGCATCTAAG[G/T]GAAATTGTGGGATCC	10529
rs189540584	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20867247	CATTAACTTTGAAAG[A/T]GTTAACATTTTTTAG	10529
rs189555686	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20842696	AAATCAATCTAAATA[A/G]TATATCCATTACCTC	10529
rs189588042	snp	A/C	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21153353	TAAGATGGAGTTTTG[A/C]TCTGTCATCCAGGCT	10529
rs189590926	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20877225	AATGTTTCATTTAAT[A/G]CTTGTGAGAATCTTC	10529
rs189600120	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	C10orf113, NEBL	GRCh38.p7	10:21147721	CGAGCACCTGTCCAG[A/G]ACATTCTATCTGGTT	10529
rs189605629	snp	A/C/G	0.000155901	0.00882768	intron-variant	NEBL	GRCh38.p7	10:20889975	GAATGATTTACATAA[A/C/G]AAGAGAAAAAGAAAA	10529
rs189619723	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20826747	AATCTCACAAATAAC[C/T]CTCTCCTGCTCTAGG	10529
rs189621095	snp	A/C	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20955064	GCATTTTAGGAAAAC[A/C]TTGCAAGAAACTGTA	10529
rs189623705	snp	G/T	0.00636936	0.0560724	intron-variant	NEBL	GRCh38.p7	10:20842403	GGGATCATAGGAAAT[G/T]AAGTATAAAATGATA	10529
rs189624822	snp	A/G	0.00517822	0.0506191	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20857636	GCTATGGGTTGAAAC[A/G]GCATTCAGCGTAGTG	10529
rs189626594	snp	A/G	0.00953873	0.0683987	intron-variant	NEBL	GRCh38.p7	10:20796356	CAAGAGTGAAACTCA[A/G]TCTAAAACAAGAAAA	10529
rs189631750	snp	A/G	0.00557542	0.0525036	intron-variant	NEBL	GRCh38.p7	10:20939433	AGAGCTCCTGAAGGA[A/G]GCACGAAACTTGGAA	10529
rs189638077	snp	A/G	0.00716266	0.059414	intron-variant	NEBL	GRCh38.p7	10:20922846	AAGGGAAAGGGAAGA[A/G]AAGATTTTGTGCTAG	10529
rs189640666	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20809779	ACAAAACCACATAAA[C/T]GGGATGAACTAAAAA	10529
rs189644362	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21085178	CCATTATATTTCTCA[C/T]GCTCCATCACATGCT	10529
rs189645963	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20889475	TATTTCCAAAATGAT[A/G]TTCAATCATTTATCT	10529
rs189648035	snp	C/G	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:20989657	GGGACTAGATAAATT[C/G]ATCAACAGAACAAAG	10529
rs189648650	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21053709	CCAACATGAAGGGTC[A/G]CGTGTGAGTGTGATA	10529
rs189651578	snp	C/T	0.00755907	0.0610114	intron-variant	NEBL	GRCh38.p7	10:21007168	AGGGGACCCAATAAA[C/T]ACCTCTAAGTCAGGG	10529
rs189665068	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21085273	GCTACTTTCTTCTCA[C/T]TGTTTTAGAGATGTG	10529
rs189665286	snp	A/G	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21034998	TTTATTTTTGAGACA[A/G]AGTCTCACTCCATTG	10529
rs189666308	snp	A/T	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:20974639	AAATAATTTTTAAAT[A/T]GTTCTTACATGTTAC	10529
rs189669280	snp	C/G	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:21117194	TGAGACCCACCAGGA[C/G]ACAATGGTTCCCTGA	10529
rs189669764	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20998405	GCTCATCGTTAACTC[C/T]CAGTAAATAATGTCT	10529
rs189676777	snp	A/C	0.00557542	0.0525036	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20855531	AAAACAAAACAAAAA[A/C]AAAACGAAGGAAAAC	10529
rs189676882	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20894634	ATTAAGCCAGAATAG[A/G]CCGGGCATGGTGGCT	10529
rs189682119	snp	A/G	0.00279162	0.0372561	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20875164	TGAGCTCATATTTTT[A/G]TCTTATTTTATTGTC	10529
rs189686605	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20893932	ATTATCAAGCTGATC[C/T]AACAGCTTTCTGCAG	10529
rs189686686	snp	C/T	0.0107246	0.0724382	intron-variant	NEBL	GRCh38.p7	10:20911039	TGTAGTGTTGTGAGC[C/T]TGTAGTTCCAGCTGC	10529
rs189693930	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21121154	TGCCTTAAAATTATA[C/T]TCTTTCATTCCTTAT	10529
rs189698027	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21067458	AAGCTTTCTTTATAT[C/T]ATAAAAAAGAGAAAG	10529
rs189703007	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20840642	ACAATCACTTACATA[C/T]AAAAGTTATAGATGT	10529
rs189704257	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21095763	CAATGAGATGTAATA[C/T]ATTCCCTTCAGCTTT	10529
rs189715365	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21109768	TCCATTTCTTGTAGA[C/T]TATCTAGTTTATTTG	10529
rs189718923	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20938712	TTAGACGAATGGCTA[A/G]CTAGAATAACCAATG	10529
rs189720541	snp	A/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20891328	ATTAGCCATAATTTT[A/T]GGTTCCTGCAAATCA	10529
rs189721677	snp	C/T	0.000798403	0.0199641	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21140068	CTGGAGACTGAGGCA[C/T]GAGAATCACTTGAAC	10529
rs189721855	snp	A/G	0.0119091	0.0762411	intron-variant	NEBL	GRCh38.p7	10:21154844	AACCTTTGTGGGTGT[A/G]TAGTAGGTGTATATA	10529
rs189724091	snp	A/G	0.00517822	0.0506191	intron-variant	NEBL	GRCh38.p7	10:20922113	GACAGAGCAAAAACC[A/G]CAAACACAAAGAAGC	10529
rs189728117	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20861795	TCCTTTGTTATTAAA[C/T]CTTGCATATGCTCTC	10529
rs189728748	snp	C/T	0.00438332	0.0466095	intron-variant	NEBL	GRCh38.p7	10:20906737	ATGAATTATAACAAA[C/T]ATAATTCAACAAATT	10529
rs189734800	snp	A/G	0.0146672	0.084371	upstream-variant-2KB	NEBL	GRCh38.p7	10:21175691	CACTGCCATGTTCAC[A/G]AGTCCACCTCAAAAG	10529
rs189734849	snp	A/T	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21128397	TCCAGACCAAAAATG[A/T]CACACACACACCCCC	10529
rs189761140	snp	C/T	0.00438332	0.0466095	intron-variant	NEBL	GRCh38.p7	10:20810421	TAAAATGTGGAATGG[C/T]GGCAAGCCTAGTTTT	10529
rs189767036	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20780174	GGGGGGAGAAAAGCA[A/G]TTGTGTTCTGTGATA	10529
rs189774599	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20805721	AGCCAAGTGTGGTGG[C/T]GTGCACCTGTAATCC	10529
rs189810261	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21156324	AAGAGTTATCAAAAA[A/C]TTAACTCAACAGTAT	10529
rs189855311	snp	C/T			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21138606	TGTGAATAATAAACA[C/T]TATTTTAAAAAAACT	10529
rs189857420	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20792182	GGTACTTTAACTATA[A/G]ATGTAATGTGAAAAG	10529
rs189858042	snp	A/G	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:20790039	TGAAAGGGAACCTGT[A/G]CTACTGTTAAATATA	10529
rs189863033	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21169694	TATCAGCTGTCTACA[C/T]ATTCATTCACTAAGG	10529
rs189863422	snp	C/T	0.00755907	0.0610114	intron-variant	NEBL	GRCh38.p7	10:20809339	CATGTAAACTATTCA[C/T]TTTACATTATATAAA	10529
rs189863762	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20993760	AGAGTCACATGGCAA[A/G]GATGTGGGCATACGA	10529
rs189864240	snp	A/G/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	NEBL, NEBL-AS1	GRCh38.p7	10:21173706	GTGCCAAAACTTCTC[A/G/T]AAGCAGGTGCAGCCC	10529
rs189876992	snp	A/C	0.00119737	0.0244387	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20869132	CAGGAACTGTTCTGG[A/C]CATACTTGATTGACA	10529
rs189879853	snp	G/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20936083	TCAAAATGACATGAC[G/T]AATTAAAGCATTTCC	10529
rs189887602	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20920437	GAAATTGTAGTCCAG[C/T]GACACACTGGAGCTG	10529
rs189904382	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20985787	AAGTGAAAGCTATAA[C/T]GAAAATTATGTTTTT	10529
rs189905599	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:20992834	CCAGGCTGGAGTGCA[C/G]TGGTGTGATCTCTGC	10529
rs189906071	snp	C/T	0.00676609	0.0577691	intron-variant	NEBL	GRCh38.p7	10:20971063	AAAAGAGACAAATAA[C/T]CTCCCAAGGTAAAGT	10529
rs189912436	snp	A/T	0.00795532	0.062565	intron-variant	NEBL	GRCh38.p7	10:21071421	CTTTCAAAGCCCTAC[A/T]AAAGGACTTTTCAAA	10529
rs189920796	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20852952	AAGCTAGCGCTAGGA[C/T]ATGCGGAAAAAGGTA	10529
rs189921980	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20990684	CCAACACTGTGCAGA[A/G]AATTTATGCAAGTTA	10529
rs189922517	snp	C/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21103170	AATAAAATGTATGTA[C/T]AGGAGCATATGAGAG	10529
rs189928944	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20790790	AAAAGGAAATCTAAA[G/T]CAATGGCTTCACATT	10529
rs189931647	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21030560	CATCTCAGAGCTCAG[A/G]CACACAGCACGAATA	10529
rs189937673	snp	C/T	0.00438332	0.0466095	intron-variant	NEBL	GRCh38.p7	10:20819836	CTCCAGCGATCCTCC[C/T]GACTCGGCCTCCCAA	10529
rs189943842	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21042188	CCTCCAAGGACTCTG[C/T]ATTTAACGTCTCATT	10529
rs189944655	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20905708	GGCATCCAAAGAGCA[A/T]TTGCAAAGACCCAGA	10529
rs189947077	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20804392	GTTTTCTTGATAAGT[C/G]GATCATTTGCTTTAT	10529
rs189952314	snp	G/T	0.00716266	0.059414	intron-variant	NEBL	GRCh38.p7	10:21008412	TTAGTTATTGTTGTG[G/T]TTTTTTATTTTTAAA	10529
rs189954300	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21028218	GCCAACAGAGCGAGA[A/C]TCCATCTCAAACATC	10529
rs189955714	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20908331	GTGATATTACTTTCT[C/T]TCATCTCCTTCAATT	10529
rs189963899	snp	A/C	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20934475	GAAGTGAGTCCGCAA[A/C]ACTGAATTCTAGCCT	10529
rs189972090	snp	A/C/G	0.00438332	0.0466095	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20958350	GGATGGCAATTAAGC[A/C/G]ACACAGTTGTGAAAA	10529
rs189981863	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20880014	ATTAGGCATCTATTG[C/T]TGTCATATTCCCCAT	10529
rs190012344	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20847776	TTCATACTGTCTTAA[C/T]CCATTTCCGTTTTGC	10529
rs190015715	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20974488	TGAGGTGGGCAAGTA[A/T]TCTGTCCACCTCAAC	10529
rs190030351	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20938891	GAAGTTTAGAGAAAA[A/G]AGAATAAAAAGAAAT	10529
rs190043375	snp	A/G	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:20821406	AGTCCAGGATCCAGG[A/G]TTCATGTTCTTTTCC	10529
rs190047287	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20887009	AGATGAGGTCCCTGC[A/T]CTCACGTAGCTGAGA	10529
rs190058227	snp	A/G	0.0119091	0.0762411	intron-variant	NEBL	GRCh38.p7	10:21076400	CAGTGAGCCGAGATC[A/G]TGCCACTGCACTCCA	10529
rs190071104	snp	A/T	0.00597247	0.0543191	intron-variant	NEBL	GRCh38.p7	10:21061187	TATATATATCATATG[A/T]TGTATTATTATAGAT	10529
rs190073033	snp	G/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21090471	TACAGGAGGATGCGT[G/T]TAGGTTATATGAAAA	10529
rs190075947	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20803169	ATTACAGCTAGACAG[A/G]AGAAATAAATTCTAG	10529
rs190082643	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20854356	GAAGAAAGCTCAGTG[C/T]TAGGAATGGAACAGA	10529
rs190103681	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20931985	CCTCATCTAAGCTAA[C/T]TGGCCACACCACTCA	10529
rs190109380	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21072549	AGGTCATACAGGCCA[C/T]GGGGCTGTCGGCTGC	10529
rs190109527	snp	A/G	0.00636936	0.0560724	intron-variant	NEBL	GRCh38.p7	10:21109114	AGCTTTTGCCCATTC[A/G]GTATGATATTGGCTG	10529
rs190115913	snp	A/G	0.00438332	0.0466095	intron-variant	NEBL	GRCh38.p7	10:21094611	CACTTGAGCCTGGGA[A/G]GCAGAGGTTTCAGTG	10529
rs190117945	snp	A/G	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21127161	TTCCTGATCCCCACC[A/G]AGGGAGGCTGCCAGG	10529
rs190119684	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21057160	CAGATCTTATGCCGG[A/G]CTTTCACATCTAAAA	10529
rs190126083	snp	C/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21086174	AGGAATTAAAGAGTT[C/G]GACTCCGTGTTGTTA	10529
rs190130357	snp	C/T	0.0232847	0.105357	intron-variant	NEBL	GRCh38.p7	10:20917518	TGTATGCAAAAAGTC[C/T]GAACTATTCACATGC	10529
rs190131172	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	C10orf113, NEBL	GRCh38.p7	10:21148337	GACTGAAACAATAAG[C/T]ATCTCTTCTGTTAAA	10529
rs190136656	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21165079	CATTCACTATTATAA[A/G]TAAAAGAGTGGACTG	10529
rs190139726	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21006504	GTGAGACCTGTAAAT[C/T]CAACCAGTCCTTCTT	10529
rs190143331	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20945577	GCACATAAAGGAACA[C/T]CTGAGTGAGATTCTC	10529
rs190151682	snp	A/G			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21135026	GCTCCACCCTCCATC[A/G]AGGGCAACGTTTGTC	10529
rs190153472	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21115152	TTATTATACCACTTT[A/G]TATATATTATAATAA	10529
rs190153980	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21011918	ATTGCAGCTGCCATC[A/G]CCTTCCACACTATGG	10529
rs190161142	snp	C/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21004057	ATTGTAACCTGAAAT[C/T]TTTTCTTATACGCAT	10529
rs190161434	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20977855	CTTGCAATGCAAGGA[A/G]TACTAAATACAGCCC	10529
rs190162978	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20986259	ACAGTTCAAAGGTTG[A/G]TTCCGCTGTTGCAAT	10529
rs190169642	snp	A/C	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21152271	TGATCATCAACGAAT[A/C]TCATAGATTGGACCC	10529
rs190171704	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:21170840	CCAAAAATATACTGT[C/G]TATGATAACATACTG	10529
rs190178774	snp	C/T	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:21067020	CTGTGTTGCCCAGGC[C/T]GTAGTGCAGTGGCGC	10529
rs190181265	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21041148	TGGTGTACAGATAAT[A/T]TTGTTAACCAGGTAA	10529
rs190183516	snp	A/C	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21040017	ATATTTTTGAAATAC[A/C]AACTGTTAGTCTGTT	10529
rs190187866	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21043980	CACCTGAAGCTCCTT[C/T]CTACAGATTCGTCTA	10529
rs190192816	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21044278	GGTGGGCGCCTGTAA[G/T]CCCAGCAGCTCAGGA	10529
rs190198359	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21080345	TGCATGAGACATATA[G/T]TTTTGACTCTTCTCA	10529
rs190202590	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21023901	GCTGCCCATACCACT[A/G]AGTTTGAAGTATCAT	10529
rs190206131	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20919782	TCCTAACTCAAAATC[C/T]GGAACCTACAGGAAA	10529
rs190215740	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21078610	ACGTATGCAGAGGTA[G/T]CTACTCCTATGACCT	10529
rs190232803	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20941319	TCCAGCATAAACAGA[A/G]CCAAAGACAAAAACC	10529
rs190242654	snp	A/C/T			intron-variant	NEBL	GRCh38.p7	10:20922387	TATTCTCCATTTATC[A/C/T]GGGATGTGTACAGTG	10529
rs190246651	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20984072	GGGAAAGGTACTTTT[C/T]AATAATGAAGTTTTG	10529
rs190276518	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20954507	TTTTCCTTAGTTCAG[C/G]TAAAGATGGGGTCCT	10529
rs190291526	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	NEBL, NEBL-AS1	GRCh38.p7	10:21174828	GCTCCCAGACCCCGC[G/T]CTTTTTAATACCTGT	10529
rs190299413	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20822127	GCACCCAACAAATAA[C/T]AGTTATTGTAATGGA	10529
rs190301402	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20901109	AAAGGTACACAGTGA[C/T]GTGAAAAACATTTGG	10529
rs190312365	snp	C/T	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:20811508	ATCCATCCAACTTAA[C/T]GTGATCCTTTTAAGT	10529
rs190323494	snp	G/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20827423	GCTTACTCTGAGAGC[G/T]GGCGCTTGCCAACTA	10529
rs190325001	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20838324	TTGAGGGGTTCAAGA[C/T]TTCAGTGGAGGAAGC	10529
rs190332976	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20872500	CAACATGGCTTCTCA[C/T]ACAGATTCCTACACG	10529
rs190342278	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20797820	ACCAGAATGAAAAAT[A/G]TAGACATGGTGGTTC	10529
rs190345355	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21108317	GCTATAAATTTCCCT[C/G]TACACACTGCTTTAA	10529
rs190351583	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20781310	TCTCAAAGTTAGTCT[C/T]GCAAATTAATCATCA	10529
rs190351847	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21106619	TGAAGTCAGGTAGCA[C/T]GATGCCTCCCACTTT	10529
rs190353004	snp	A/C/G/T	0.000132157	0.00812795	intron-variant	NEBL	GRCh38.p7	10:20831458	TTTAAACTTTGTATC[A/C/G/T]TGCTGCTGTCTTACC	10529
rs190356740	snp	C/T	0.00676609	0.0577691	intron-variant, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20873598	AATTTTAGACTATTA[C/T]GTACCATATTAAGGA	10529
rs190356979	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20888409	TTTATCATAGAGAAC[A/G]CTTTCAATGAGACAT	10529
rs190361973	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21090637	AACACTTTTATTTTG[A/G]TACTTATCCAACTCA	10529
rs190365498	snp	A/G	0.00398564	0.0444627	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20849371	TCAATCAAATACGCC[A/G]CCTATGCTTTGAATG	10529
rs190367555	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20902653	TCTACATTAACATAG[C/T]GCCCATTGAGCTGAA	10529
rs190384220	snp	A/G	0.00279162	0.0372561	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21144545	AGCCTGGCCAACCTG[A/G]CAAAACCTTGTCTGG	10529
rs190384404	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21160068	CCCAGAGAAAGAAGC[C/G]AGACTTGGGAAGCTT	10529
rs190385432	snp	A/T	0.00914312	0.0669923	intron-variant	NEBL	GRCh38.p7	10:20787503	TAATTAGGGACACAT[A/T]AAGAAACTCAGCTTA	10529
rs190385833	snp	G/T	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:21122005	GGGATTTCTCCTGGT[G/T]GTTGTTGTTGTTGTT	10529
rs190387943	snp	A/G	0.00795532	0.062565	intron-variant	NEBL	GRCh38.p7	10:20816903	CAAAAATGGAGTCAT[A/G]ATTGTGGGAAGTGGA	10529
rs190389171	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21150734	ACAAAAGTCACACCC[A/G]AAGCCAACAGCATGG	10529
rs190389835	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20854952	TTTTTTGGCTAGGCG[C/T]GGTGGCTCACACCTG	10529
rs190392285	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20801653	ATCTCACACATACAA[C/G]AGATACTAGATAAAT	10529
rs190395799	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21048500	AGAAACAATAGATTT[A/G]GCACCACATGAGTTT	10529
rs190401957	snp	A/G	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20988744	TCTTACTTGGGCATG[A/G]GCACACTGCAAGCAG	10529
rs190425314	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21026257	CTCATTTGGGAGTGA[A/G]TAGGGAGGGGAAAAT	10529
rs190446444	snp	A/C	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21060663	TTTTCTCTTCCCTGT[A/C]TGCAAAACTCTTCAA	10529
rs190456226	snp	C/G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21030953	ACCATTAGGACACAC[C/G/T]GGTGTGCACTGATGA	10529
rs190474281	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21062923	AAGAGAACAGAGAAG[A/G]ACACGAGCGGCCAAG	10529
rs190483657	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21090019	CCAGCCCAGATCTCT[A/G]CCCCAAGTCCCAGCT	10529
rs190492138	snp	G/T	0.0103295	0.0711199	intron-variant	NEBL	GRCh38.p7	10:20918818	ATTGCACCACTGCAC[G/T]CCAGCCTGGGTGACA	10529
rs190493236	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21001071	CCCCATGAGCTTGTA[C/T]AGATCCTCCCTTCTC	10529
rs190500874	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20968091	CAGAAAGTTAAATCG[C/G]CCACTCTGAGTTTCT	10529
rs190512660	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20949338	CATTAGGACAAATAC[C/T]TAATGCATGCGGGGT	10529
rs190518654	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20835379	CTGGCATAATGCTTC[A/G]GAATAGTCTCCATTC	10529
rs190541111	snp	A/T	0.00874735	0.0655527	intron-variant	NEBL	GRCh38.p7	10:20942762	AAACAAACAACCCCA[A/T]CAAAAAGTGGGTGAA	10529
rs190547997	snp	G/T	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:20928634	TTCTGCTTTCCCTTC[G/T]GATCCAATGGAAGGA	10529
rs190558986	snp	C/T	0.00398564	0.0444627	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20848359	CCAAATTCACTAGTA[C/T]CAATTCACTTGAAAC	10529
rs190559436	snp	C/T	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:20807900	ATCCATCAGCCTGGA[C/T]ACAGAAAACAGAAGA	10529
rs190559779	snp	A/T	0.00716266	0.059414	intron-variant	NEBL	GRCh38.p7	10:20806304	TCATTTAGGACCTAA[A/T]TCATAGACTTGGATG	10529
rs190569836	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20914830	GGTAATGGTTCTCAA[G/T]ATGTATTTTTCATAT	10529
rs190576583	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20816151	TTGAGTTGTATTTAA[A/C]ATGCTGGCATCTTAA	10529
rs190586748	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20830951	GGTTTAATGTCCTTG[C/G]ACTCAAAACAAGGAG	10529
rs190587237	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20869920	TAGTGTTCATAACAT[G/T]ATTTATTCTCATAAT	10529
rs190590210	snp	A/T	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21125453	GAGGGGACTACTTAA[A/T]GAACTGGGCTATTTA	10529
rs190592915	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20794179	AGCGGACCCCATTTC[C/G]TTGGGGTGGAGCAGA	10529
rs190602843	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	NEBL, LOC102725112	GRCh38.p7	10:20885109	GTTAAAGAGACTTTT[C/T]ATTAGAACCCAGAAT	10529
rs190603397	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20816736	TCTTGAACTGCATCC[A/G]TGAATTATTTCAACA	10529
rs190610780	snp	A/T	0.00795532	0.062565	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20898628	CTGTACCCCAGTCTC[A/T]GTCCCTGCCACTTAG	10529
rs190621520	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20786434	GAGAAATTTAGCATA[C/T]AAGTGTCCTGAATGT	10529
rs190627577	snp	A/C	0.000798403	0.0199641	intron-variant, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20853075	AAAAAGAACAGAGGA[A/C]AAGAAACCCAGAGGC	10529
rs190642626	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21076621	AACCCACGTGTCCAT[C/T]AATGAATGAATCAGA	10529
rs190644856	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21167811	AGTGTTATTTTCTCG[A/G]CACCTCTTAGTGATA	10529
rs190664343	snp	G/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20932738	AAAACCATTTTATTT[G/T]TCGATACTAATCGTT	10529
rs190677896	snp	G/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21166607	CAGACACCAGGCTAC[G/T]GCCTATCCTAGTGTT	10529
rs190708138	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20966301	CGCTAAAGCAAGAAT[C/T]AAGAAACCTGAATTT	10529
rs190716633	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21075848	CAAAATAACGAACAA[C/T]CCCATTTAAAAAAGG	10529
rs190718555	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20903064	CAAATTATAGTAGCC[C/T]CCAGACCTTATCCAT	10529
rs190726986	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21105882	ATGATCACCATTCTA[A/C]CTGGCATGAGATGGT	10529
rs190729500	snp	A/T	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20933194	GGTTCACCATTTGCA[A/T]CAGTCCCTCCTGACC	10529
rs190734565	snp	C/G	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21130425	GACATGTATAGACTA[C/G]TTTACCCAACAACAG	10529
rs190736527	snp	A/G			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20884359	TGGGATTACAGGCAC[A/G]AGCCACAGCATCTGG	10529
rs190737775	snp	A/G	0.00199481	0.0315187	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20880736	GCAAAATAAACATAA[A/G]CCCTAATATGACTTA	10529
rs190754474	snp	C/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21050169	TCTTTGGTTTCACCA[C/G]GTAGAGTCTCTCTTT	10529
rs190759963	snp	C/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20849013	CATTTCTGCCTGTTT[C/T]GATGTTGTTATTGGG	10529
rs190771615	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20933695	GCCAAGATCACACCA[C/T]TGCATTGCATCCAGA	10529
rs190779653	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20906553	GCTTTAAAATAACTG[C/G]TACTCTCTGAAGAGT	10529
rs190782574	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20914422	TTCTATGAGATTACC[C/T]TCTATGTTTCCTATA	10529
rs190784097	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20904296	CATTTCAGCATTCCT[C/T]ACTATGCATTTATAT	10529
rs190789339	snp	C/T	0.00874735	0.0655527	intron-variant	NEBL	GRCh38.p7	10:20940118	ACTCTCCACCCCAAA[C/T]CAACAGAATATACAT	10529
rs190791047	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20982590	ATTTCTGTTGAAAAG[A/G]TGTTTTCTGGATTAT	10529
rs190793062	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20965314	AAGAGAGAAAAATAG[C/T]GAGACAAGGGGACGT	10529
rs190801052	snp	A/G	0.000798403	0.0199641	intron-variant, nc-transcript-variant	NEBL	GRCh38.p7	10:20819165	TGACTTCATCACCCC[A/G]GCATTAAGCCCAGTA	10529
rs190806473	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20946333	GAAGCTGTGGCCCTC[A/G]TGCTACTGGTAGTTA	10529
rs190810016	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20942282	CCCTCAGAAATAATG[C/T]CGCATATCTACAACC	10529
rs190812426	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21016860	TAGATACCTACCCAC[A/G]TTTTTGCAAAAATGG	10529
rs190818077	snp	C/T	0.00755907	0.0610114	intron-variant, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20884776	GAGTAGCGTGAATTG[C/T]TTCTATGATAAGGCA	10529
rs190820655	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21035234	AACTCCTGGCCTCAA[A/G]TGATCTGCCCGCTTC	10529
rs190826573	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21089855	GGTTTTCCAAAAACA[C/T]GTCCATAGTTCCAAT	10529
rs190834909	snp	C/T	0.00517822	0.0506191	intron-variant	NEBL	GRCh38.p7	10:20999256	TTGATTGCCCAATTA[C/T]GTGTGAGAAGACCTG	10529
rs190836398	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20798729	AAATCAACTCAGCCT[C/T]ACAGGAAATGTATTT	10529
rs190837314	snp	A/C	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20980067	AAAAAAAAAAAAACA[A/C]ACCATAAAATTCACC	10529
rs190838971	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20800488	TTTGGGTTGGGTATA[C/T]ACCAGAAGAGGAACT	10529
rs190846523	snp	A/C	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20828719	GGCAGGAAAGGAGGA[A/C]GGGAGAGAGAGAGAG	10529
rs190851293	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20960817	CTGGAAATTAAGGCT[A/G]CATCAGTTATAACAC	10529
rs190855439	snp	A/G	0.00835141	0.0640778	intron-variant	NEBL	GRCh38.p7	10:20943334	TCTCAGCAAACTATC[A/G]CAAGGACAAAAAACC	10529
rs190863873	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21055544	CCATTCTGCATGTAA[C/T]CACATCCTGGCTCTA	10529
rs190865717	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21014197	AGTGTGATCGTAGCT[C/T]ACTACAACCTCAAAT	10529
rs190865986	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21032451	GTTGATGCGATGTCT[A/G]TTCATGAATTTCCTT	10529
rs190871655	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21071969	GACTACAGGTGCCTG[A/C]CACCACACCCAGCTA	10529
rs190873889	snp	A/C/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20994886	GAGGAGGAGGTAGAG[A/C/G]GGGGGGTTGGTCTTG	10529
rs190880341	snp	A/T	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:21038451	CCACTTATGAGTGAG[A/T]ACATGCAGTGTTTGG	10529
rs190900910	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21039341	CTAGGTTTTCTTCTA[G/T]GGTTTTTATGGTTTT	10529
rs190912334	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21072232	GGTCACTTCAATCCC[C/T]ATCTTAGTCTCCTCA	10529
rs190913654	snp	C/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20929683	GTTCTCATTTACAAG[C/T]GGGAGCTAAATAATG	10529
rs190922044	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21103473	CCACCTTGGCCTCCC[A/G]AAGTTCTGGGATTAC	10529
rs190927291	snp	C/G	0.00478085	0.0486577	intron-variant	NEBL	GRCh38.p7	10:21148932	AAATTCTCTGATGTC[C/G]ATTGTCTGACTGTGG	10529
rs190946459	snp	A/T	0.00636936	0.0560724	intron-variant	NEBL	GRCh38.p7	10:20979213	GCTTGAGACCAGGAG[A/T]TGGAGACCAGCCTGG	10529
rs190967003	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21003171	CATAAAATCCCTAGA[C/G]CACAGCTCTTCTGCA	10529
rs190969753	snp	A/G	0.0103295	0.0711199	intron-variant	NEBL	GRCh38.p7	10:20946836	AGATGTGGAAATCCT[A/G]GCAGCATTTAACAAA	10529
rs190975114	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20918085	AGCTCCAGGCCAGGT[A/G]CAGTGACTCATGCCT	10529
rs190987511	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21085451	ACAAAATGAGAACCT[A/G]TCTCTACAAACAACA	10529
rs190996042	snp	C/G	0.0111196	0.0737302	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20859065	AAGAAAGCAACAGAT[C/G]AATAATACATAATTT	10529
rs190996266	snp	C/T	0.00398564	0.0444627	intron-variant, upstream-variant-2KB	NEBL, LOC102725112	GRCh38.p7	10:20844304	TCCTCAGTTCAAAAA[C/T]TCAAAATGAAATGAA	10529
rs191003236	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20955309	CCAAAGTGGAGAATA[C/T]GATGTGTGAAATGAG	10529
rs191006987	snp	C/T	0.00835141	0.0640778	intron-variant	NEBL	GRCh38.p7	10:21103299	GCCCACTGCAAGCTC[C/T]GCCTTCCGGGTTCAT	10529
rs191009836	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20878173	GAAATTCATCCATAC[A/T]GTCACATGAGCCCTC	10529
rs191012033	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:20812482	CCCCTCCCCCCACCT[C/G]ACAACAGGCCCTGGT	10529
rs191012363	snp	A/G	0.000264603	0.0114992	intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20831215	CTATAGATTTCAGAT[A/G]TCCTCTTGGCTCGAA	10529
rs191016583	snp	A/G	0.00597247	0.0543191	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20864298	AATCCCTTCATCTTC[A/G]CATAGGAGATTTTTG	10529
rs191024087	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20798433	GTGGAGATCACATTA[C/T]GACTCTACTGTTTTG	10529
rs191043136	snp	G/T	0.0115144	0.0749975	intron-variant	NEBL	GRCh38.p7	10:21083656	TCGAGAACAGCCTGG[G/T]CAACATGGCAAAATC	10529
rs191052536	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21113977	CTTGCTCTTCTTTTT[C/G]TAGTTTCTTATGGTT	10529
rs191052700	snp	G/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21161755	TCAGGATGTAAAGAG[G/T]CAACCCATCAAAGGT	10529
rs191055282	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NEBL, LOC102725112	GRCh38.p7	10:20844767	CAGACCTTCACATGT[A/G]AGCATCTTATTTCTG	10529
rs191058437	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21100375	AAAATGAGGAGCTCA[A/C]TCGCAAACTCTGCTC	10529
rs191060670	snp	G/T	0.00119737	0.0244387	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21134360	TGTATTCTTATTTTC[G/T]ACAGTATTTTTGTTT	10529
rs191068167	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20927113	CAGAAGCTCAGGAGC[A/G]GAGGATAACTAAGTT	10529
rs191069016	snp	A/G	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:20894916	CCTGGGTGATAGAGC[A/G]AGACTCTGTCTAAAA	10529
rs191070089	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20897637	GTTATCTCAAAGATT[C/T]CTTGTCTCTGTCTAA	10529
rs191073160	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20923177	ATCTCAATCGATCCT[C/T]CAGCCTCAGCCTCCC	10529
rs191074411	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20878484	GCTGAACTTTTACAG[A/G]AGACAGGTTTATGGG	10529
rs191094515	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21156274	TTGTAAGCACGGGGC[A/C]AAAAAGTACAAATGT	10529
rs191100897	snp	A/G	0.00716266	0.059414	intron-variant	NEBL	GRCh38.p7	10:20794701	AGACTCTACTTCCCC[A/G]GGAATACTGAATCTG	10529
rs191103295	snp	C/T	0.00199481	0.0315187	intron-variant, downstream-variant-500B	NEBL	GRCh38.p7	10:20813245	AAATCCTGGTTACTT[C/T]CTAAAATATACTAAT	10529
rs191110518	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21050639	GGCTTAATTTGACTG[C/T]GTAGATTCCAAGGGC	10529
rs191116422	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21068239	TTTGTCAGCACTTTT[C/G]AATAAACAGGTTTAA	10529
rs191123897	snp	C/T	0.00716266	0.059414	intron-variant	NEBL	GRCh38.p7	10:21035764	CATTTTCTTCTCAAA[C/T]GGCAAACCTCCCACC	10529
rs191134786	snp	A/C	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21051197	CCTTACACAAGAAGC[A/C]AATCAGAGCTTTGCG	10529
rs191137571	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21056373	ACAATCAGGAGTTAC[C/T]AAATTTGCGCAAAGT	10529
rs191144254	snp	G/T	0.00438332	0.0466095	intron-variant	NEBL	GRCh38.p7	10:21023306	GTTACAGAAAGTTTA[G/T]CCCGTTGAGAGATCC	10529
rs191160080	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21083941	AGCGTACCTTTTCTT[A/G]CTGAAGAGCCTATGG	10529
rs191168341	snp	A/G	0.0260105	0.111035	intron-variant	NEBL	GRCh38.p7	10:21106175	TTCTTTTGCTGTGCA[A/G]AAGATCTTTAGTTTA	10529
rs191172305	snp	A/G	0.00358779	0.0422022	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21144023	CAACAAGGAGAGAAG[A/G]ATTTTTGCTTCAAGT	10529
rs191175464	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21085672	AAATAAAACAACATA[C/T]ATACAAAAGCTCATT	10529
rs191195865	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20959420	CAAAAAATATCTGTT[C/T]GGGTTTTAGCCAATA	10529
rs191214535	snp	C/T	0.0103295	0.0711199	intron-variant	NEBL	GRCh38.p7	10:21119616	ATAAATGTGAACTGC[C/T]TGAAAGTTAGTAGCA	10529
rs191235000	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21031734	TTCTTTCTTTCCCAC[C/T]GGGAGCCCAAGTTGT	10529
rs191240094	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20974728	GTGTCCATCAAATGA[A/G]TAAATAACTAAGATA	10529
rs191259903	snp	A/G	0.000214903	0.0103636	intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20808621	AAGTACTGCTGGAAT[A/G]GGATCGAGACCAGTG	10529
rs191280465	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21064537	TTACAAGTCTCGTTT[C/T]ATTAACCATTTAAAA	10529
rs191281236	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20789069	ACAAAAACAATTGCT[C/T]TCCTGGAGCACCGAG	10529
rs191281411	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20824376	ATCATCTATGTCTTA[A/G]TATCTGTGGATTTCA	10529
rs191285343	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21081054	CAAACAGTATTTCAC[C/T]ATGTTGGCCAGGCTG	10529
rs191293827	snp	A/C/G	0.00239393	0.0345281	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20853635	TCTACAAAAAATAAA[A/C/G]AAATCAGCTGGGCAT	10529
rs191296290	snp	C/T	0.00318978	0.0398085	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20871625	TTATAATCATGAATC[C/T]GTCTGACAAGTGAAC	10529
rs191301473	snp	C/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20885710	ATAAAAGCAATAATA[C/G]ATTGTTTTCCTTTTC	10529
rs191305425	snp	C/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20864675	CCTGTTATTAAATCC[C/T]TAAATCATTTGCCTT	10529
rs191306893	snp	A/C	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20939949	GCAAGTCCTTAGAGA[A/C]CCAGAAAGAGAATTA	10529
rs191310316	snp	A/T	0.000798403	0.0199641	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20881104	TCTACCTCTTTGTTG[A/T]TTACTTCAAAATGTC	10529
rs191314375	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20805252	GGTGGTATTGAACTT[A/G]TAAGGTTTGATATAT	10529
rs191322582	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20837274	ACCCCAGTGAACACA[C/T]GAATTATAAGAATGT	10529
rs191324033	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20911375	ATTCAACACAGTTAA[A/T]TGTATATACCCGTTG	10529
rs191324330	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21158772	TTAATTTCTTAATGA[A/C]GTTTTGGATCTTTTC	10529
rs191324920	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20820854	AAATAAAAAAGAAAG[A/G]AAGAAAAGAAAAAGA	10529
rs191329807	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20839831	AAAAAGGGATGTTCA[C/T]TTCCCATTGGGATTA	10529
rs191335595	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20912184	CAACACAACTATTTT[G/T]TATATTGCTTCTGTT	10529
rs191337023	snp	C/T	0.0023933	0.0345097	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21138578	AGGACAGAAACACGA[C/T]AAAAATGGGAAGTGT	10529
rs191337178	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21153005	CTTGGTGGATTTTAT[A/C]TGGCTGAGAAACTCC	10529
rs191337929	snp	C/T	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:21155137	CCAGGAGGCAGAGGT[C/T]GCAGTGAGCTGAGAT	10529
rs191347039	snp	C/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20791843	CTGGGGGGGATGTAC[C/G]CAGAGTGCGTGAAAG	10529
rs191348009	snp	C/G	0.00636936	0.0560724	intron-variant	NEBL	GRCh38.p7	10:20807662	TAAGTTGCTCAACCT[C/G]AAAATTTCCTACCTT	10529
rs191353126	snp	G/T			intron-variant, upstream-variant-2KB	NEBL, NEBL-AS1	GRCh38.p7	10:21173016	GCTTGTTCTAAGGAA[G/T]CATTTGTATCTTCAG	10529
rs191360963	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20924791	GAAAGAGATTACAAA[C/T]GGTCGTTCAGTTCCA	10529
rs191382158	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20791123	GAAAATACACAGAAG[C/T]GTGACTCAACTTTCA	10529
rs191397650	snp	G/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20843380	TACAATACAGTGTTC[G/T]GAGCCCTTTCCTACC	10529
rs191411093	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21069320	AAATGAAATGGGGCC[A/G]TTTATGGCAGGCACA	10529
rs191412982	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21101068	TCCTTCATTCACAGG[C/T]CTGAAGCAGAAGTGG	10529
rs191417129	snp	A/C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21122704	GGATGGTGCAAAAAT[A/C/T]CTCAGTGTCTGGGTA	10529
rs191441455	snp	A/G	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21132102	ATTTTCATCACCCCA[A/G]AAAGAAACTCAGTAC	10529
rs191456800	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21103580	AGTGGTTTTACTTTG[C/T]ATCTACTTAATGACT	10529
rs191459408	snp	G/T	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21140684	TATAGTTTTCAACTT[G/T]AATAAATCAATACTA	10529
rs191482449	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20967229	CCATCCACATGAGAA[G/T]GAATAAATCCAATGT	10529
rs191486418	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20948625	CAACAGACACACACT[C/T]ACGCTGGAGGACACA	10529
rs191492453	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21013890	TAAAACAAAAAGAAC[A/C]CAATGAAGAGCAGAG	10529
rs191497740	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20933384	TTACCCGTACACTAC[C/T]AGACTATATGACTGA	10529
rs191510349	snp	A/G	0.00438332	0.0466095	intron-variant	NEBL	GRCh38.p7	10:20994479	TGTAACTAATTCAAC[A/G]TCTTTTTGCATTCAA	10529
rs191512536	snp	A/G	0.00478085	0.0486577	intron-variant	NEBL	GRCh38.p7	10:21044984	CTAGTGAAAATAAAA[A/G]AAGTATAATTGGCTT	10529
rs191517582	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20983503	AAAACCTCTCTTTCC[A/G]TAAGTATTCCAATTT	10529
rs191518382	snp	A/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20959772	TAACATTAAGACATC[A/G]CAAAAAGTTTTTTTT	10529
rs191527814	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21014525	CTTTGGACAGTCAAT[A/G]GAGTTCTTCAGTCAG	10529
rs191530437	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20889592	CTTTTCAAGAGGAAT[C/T]GTATATAAATAAGAA	10529
rs191534601	snp	A/G/T	0.00517822	0.0506191	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20867303	CCAACAGAATAGTAC[A/G/T]TCTTTTCATTTGTTC	10529
rs191535886	snp	A/C	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20973471	CCCAGGCTGGTCTCA[A/C]ATTCCGGGCCTCAAG	10529
rs191536748	snp	C/T	0.00755907	0.0610114	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20851677	GTAATCTCTGCTACT[C/T]GGGAGGCTGAGGCAG	10529
rs191540660	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20903856	GTACTGTAACGGCCA[A/G]TGGAGACTCAGAAGG	10529
rs191541990	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20952864	AAGCCGAGATTGCAC[C/T]GCTGTACTCCAGCCT	10529
rs191550851	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20918272	CTGAGGCAGGAGAAT[C/T]GCTTGAACCCAGAAG	10529
rs191553790	snp	A/G	0.0134861	0.0810011	intron-variant	NEBL	GRCh38.p7	10:20818364	GACTCAGTTTCCCAC[A/G]TCTACCAACCAGAGA	10529
rs191556758	snp	A/G	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20823105	ACCGATCCTCTCGCA[A/G]TGAGGTTCATTGTGA	10529
rs191557086	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21065089	TACTGAACAATAAGA[C/T]TTTCTTCTTGATAGC	10529
rs191566425	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20820034	GAATTCATTTCTTCA[C/T]AGCACTAAAGCAACA	10529
rs191567283	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20834430	AACACTTATTGATCA[A/G]GAAACCTATACCATC	10529
rs191567840	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21033153	GCCCTGTGATTTGTG[C/T]CCAGGAACACCAACC	10529
rs191569714	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20987791	TTTCCAGGGCTCCTT[A/C]TGTACCAGCACCCCT	10529
rs191571639	snp	A/G	0.00676609	0.0577691	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20875521	ACACATGTGCAGCTG[A/G]AGGATTCACAGTGGC	10529
rs191572233	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21004994	GGGTAGGCCATTTAA[C/T]AGAGGCAAAAAAGGA	10529
rs191572646	snp	C/T	0.00557542	0.0525036	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20877659	CTTTCCAACCATGTG[C/T]GCAGTAGGGAGCAGA	10529
rs191574106	snp	A/C	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21047176	GCAGATCATCTATTT[A/C]GTCACTTTTACTCAA	10529
rs191581165	snp	C/T	0.00478085	0.0486577	intron-variant	NEBL	GRCh38.p7	10:20908057	CTCTCCACTGACCTA[C/T]ACCAGGTACCGAGAA	10529
rs191593074	snp	G/T	0.00676609	0.0577691	intron-variant	NEBL	GRCh38.p7	10:20917900	TTAATTGTGTTAAAA[G/T]AAAGATGATATTATA	10529
rs191595660	snp	A/G	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:20938530	TCTAAAAATCAGAGC[A/G]CCTCTTCTCCTTAAA	10529
rs191597140	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20793744	TGTTTTTCATAGAGA[C/T]GGGGTTTTTCCATGT	10529
rs191604155	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20921724	CCTTAATATGTGACA[A/G]CACACACACAACACA	10529
rs191608228	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20855183	GCAGTGAGCTGAGAT[C/T]GTGCCACTGCACTCC	10529
rs191631320	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20889000	CCTTCTGCTACCACA[A/C]TCTTTGGATTTTGGT	10529
rs191637714	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20824011	CATCACATATATTTA[A/G]AGGAAGATCAATCAG	10529
rs191646365	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20804586	AGGCCCACTGAAACA[C/T]AAAGAAAAATGGCAC	10529
rs191671939	snp	C/T	0.00438332	0.0466095	intron-variant	NEBL	GRCh38.p7	10:20799968	CGGAGAAAGAGAGAG[C/T]GCACGCGTGTGAGAG	10529
rs191691067	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21151715	CCACACGCCCCAGGT[A/T]CACTCCGTGCCCTTG	10529
rs191691953	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21092097	AATCTGATAATGGAA[A/G]AGTTCTGTTCTCAAT	10529
rs191695215	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21067927	AAGGCTGCAGTGAGC[C/T]GTGACTGCACCATGC	10529
rs191698990	snp	A/C	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21042613	CACTGTTCTTTCCAA[A/C]TTCAGATCATGTAAT	10529
rs191701543	snp	C/T	0.0479149	0.147179	intron-variant	NEBL	GRCh38.p7	10:21077569	CCGAGATGGCACCAC[C/T]GCACTCCAGCCTGGG	10529
rs191711397	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21106980	ACTCATGATTTGGCT[C/G]TCTGTCTGTTATTGG	10529
rs191712719	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21009267	TTTGTATAAGTAAAT[C/T]GCTTGGAATTGGTAT	10529
rs191715716	snp	C/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21100029	TTCCCTTAAAAACAC[C/G]CCCAATAACCTGGCC	10529
rs191737223	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21010781	AGGTTACTGAAGCTC[A/G]ACAACTGAGTTAAAT	10529
rs191740532	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20962169	ATACCATTACTACTG[C/T]GAAAGGAAAGAAAAT	10529
rs191744807	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:20944511	AGATTTTCTGTGTTT[G/T]CATGAGAACTAATGT	10529
rs191745065	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21030465	CTAAATCTACCAAAA[C/G]TGATCAGCCCCAAAA	10529
rs191749364	snp	G/T	0.0162398	0.0886349	intron-variant	NEBL	GRCh38.p7	10:20972548	AGGAGATCAAGACCA[G/T]CCTGGCCAACATGGT	10529
rs191754500	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20930608	GTTCCCCTTTTGCTC[A/G]GTCCAGCTTTCTCTC	10529
rs191764833	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21062167	GTGCCAAGTTTTTAG[C/G]ATTTCAGCAGGTGCA	10529
rs191769461	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20975783	CACTAGCAAAATGAG[G/T]AATTTTCTGCTGAGG	10529
rs191772861	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20979748	CTCTCACTCTGTCAC[A/C]TGCGCTGGAATACAG	10529
rs191777295	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21043801	TATATTTATTCAACA[C/T]AGATGCATCAGACTA	10529
rs191793532	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21022791	TGTATAACCGCTGGA[C/G]TGTCAAGAGATAATT	10529
rs191810767	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20985484	GTCTCTAACATTCTA[A/G]TAAGATTATCTTCAT	10529
rs191812869	snp	A/C	0.00676609	0.0577691	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20858730	CCCATCCTATCACCA[A/C]AGGCTTTTTTAAAGC	10529
rs191816010	snp	A/C/G	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21073936	AAAAATTAGCCGGAC[A/C/G]TGGTGGCGGGTGCCT	10529
rs191835227	snp	A/C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20899514	AAAAACCAAACACCA[A/C/T]GTGCAATGTGAACAC	10529
rs191850358	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20890923	CTCTGTAATATGCTC[A/G]TGTTTATCCTCCCAA	10529
rs191863213	snp	C/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20902853	CTTGACTCCCACAGA[C/G]TGTCCCTTTCCTAGA	10529
rs191876827	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20920084	TGGTGATAAGAGAAA[C/T]ATAAATTAAAAGAAC	10529
rs191891672	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21148569	TCTCACTCTGTTGCC[A/G]GGCTGGAGTGCAGTG	10529
rs191904082	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21089396	GGACTCCAAGACTGC[A/G]TTGGAACAAAGTGAC	10529
rs191904228	snp	C/T	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21129181	AAAGAAAGAAAATGA[C/T]GAAGGTCAGGAACTT	10529
rs191908320	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20874084	TGGTTTCTTCCATAG[A/G]AACACCTAGAATTAT	10529
rs191911643	snp	A/G	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:21110685	TGCCACCACCCCATG[A/G]AAGGCTCAGTGGACA	10529
rs191915088	snp	C/G	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:21149673	CAAATTAACAGAATC[C/G]AAGGACAGAGTTCTG	10529
rs191927122	snp	C/T	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:21105350	CAGTCCCCTACCCCC[C/T]GACAGGCCCCAGTGT	10529
rs191932335	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21167073	ACACTCAACAGGGGC[C/T]GGCAGAACTGTGCTG	10529
rs191936408	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21080653	ACTAGGACTACAATG[C/G]AAAAGAAGCAAGGCT	10529
rs191939772	snp	A/T	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:21046374	GAAAATAGATTTTGT[A/T]GTGTTATACGAGGTA	10529
rs191940412	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20840379	GACTGGGAGAGTCAG[A/T]TGGGTTATGAGTGGC	10529
rs191949874	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21069809	ATTATTGTATTCATC[C/T]GATCATTATCTAACT	10529
rs191955088	snp	A/G	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:21125011	ATCAGTCTCCACTGA[A/G]GTGCAGTGTTGAGAG	10529
rs191964192	snp	A/G	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:21109496	CAGGTTTTGGTGTCA[A/G]GATGATGCTGGCCTC	10529
rs191970393	snp	A/C	0.00318978	0.0398085	upstream-variant-2KB, intron-variant	C10orf113, NEBL	GRCh38.p7	10:21147173	ACTACATCCACGCAC[A/C]TCTTCCCCAAAGCAA	10529
rs191975644	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21162745	GTGATATAATTGAGG[C/G]ATAAAAAGTACAATG	10529
rs191984597	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21028629	AAGGTTAGAATATTA[C/T]TGAATTTTAGATTTT	10529
rs191987330	snp	A/G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20886395	TTAGCTGGGTGTGGT[A/G/T]GTGTGCGCCTGTAAT	10529
rs191996180	snp	A/G	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:21151959	GCTCCACGAGGGCAG[A/G]AATTTTCCTCTACTT	10529
rs191998551	snp	A/G	0.00914312	0.0669923	intron-variant	NEBL	GRCh38.p7	10:20900878	AAAAAAATTAGCCGG[A/G]CATGGTGGCACACAC	10529
rs192009644	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20915855	CCCAAGGGCAGGCTC[C/T]GAAATTTTTAAACTT	10529
rs192016962	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21027906	AAATGGTTGTTTTAT[A/G]TCATTCAAAATTATC	10529
rs192020309	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20999528	CACTTGAGCCCAGGA[A/G]GTTGAGGCTGCAGTG	10529
rs192020481	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21082936	CCTGGCTAATTTTTG[A/C]ATTTTTTTAGAGACG	10529
rs192027307	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21061430	TATCATATATTGCAT[A/G]GTGTATGATATATAT	10529
rs192031823	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21112730	CATGTACCCTAGAAC[A/T]TAAAGTATAATAAAA	10529
rs192050211	snp	A/G	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:21107728	CTACAGATTGAAATA[A/G]TTTTGGAAGGAATGG	10529
rs192055120	snp	C/G	0.00676609	0.0577691	intron-variant	NEBL	GRCh38.p7	10:21093521	AGCTGCTAAGCTTGT[C/G]TAAACTGAATGCCAT	10529
rs192065973	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20991094	TTAATAAACAAAACC[C/T]ATAGAGAAGTATGAG	10529
rs192083003	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20955745	GTGTTTTAGATGCAA[C/T]GAAAGGAACAGAAGG	10529
rs192086840	snp	A/G	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20803525	AATTTAAAAGAATCA[A/G]CAACATCCAGAAGAA	10529
rs192090287	snp	A/G			utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20782098	TAGATGGAAGAAGTC[A/G]GCATTTTCTAAAGTT	10529
rs192092240	snp	A/G	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:21002544	ATAAAGAACTGAGAC[A/G]GGGTAATTTATAAAG	10529
rs192114548	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	NEBL, LOC102725112	GRCh38.p7	10:20845559	CCAAACAAAGGAGAA[C/T]TATTAAGTGGACTCT	10529
rs192114818	snp	G/T	0.133435	0.221162	intron-variant	NEBL	GRCh38.p7	10:20829439	TGGGGACTGTTGTGG[G/T]GTAGGGGGAGGGGGG	10529
rs192135215	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20798991	ACTTTTTCTTAGGGA[A/C]GTAACAGAATGAACG	10529
rs192144519	snp	C/T	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21141904	TCCAGGATTATTCTC[C/T]CACTCCACCTCCCAC	10529
rs192147193	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20782974	GTATCAAACTGTTCC[G/T]TGTGCTTCTGTCAGG	10529
rs192147583	snp	A/C/G	0.000134804	0.00820885	intron-variant, nc-transcript-variant	NEBL	GRCh38.p7	10:20813894	CCGTGCACTGGATCC[A/C/G]CCCATTCCTTAGCAT	10529
rs192148901	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20915211	CACCAACAAATACTT[A/G]TTAGACATTTATATA	10529
rs192159592	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20865812	ACAATTACTATGAGG[A/C]ACAATTGCATTTGGG	10529
rs192163788	snp	A/G	0.0236746	0.106192	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20882330	AAAGAAGAGGGGAGA[A/G]GAGAGAGGAAAAGGA	10529
rs192163861	snp	G/T	0.00010118	0.00711196	intron-variant	NEBL	GRCh38.p7	10:20826562	ATAAGAAAAGGAAAA[G/T]AATAACTAAGCTTGT	10529
rs192166750	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20970701	CAACAATAATTACAA[A/G]GTACATATATCATCT	10529
rs192174219	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20895067	ACGTGGGTGTGAAAT[C/G]TATGGATTTAGCTTT	10529
rs192182233	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20796037	CATTACATTTCAGCA[C/T]TTCATTGATATATTT	10529
rs192183550	snp	C/T	0.00676609	0.0577691	intron-variant	NEBL	GRCh38.p7	10:20935331	CAAGACTGTGCTTAA[C/T]ACGACAACTGGCAAC	10529
rs192184326	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20832423	CAACAAATAAGTTAT[A/C]TCTGTTTTTTTTTTA	10529
rs192193218	snp	C/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20850590	ATGTTCTAAACTAGT[C/T]ATCTTGTTGTCTAAA	10529
rs192193707	snp	A/G	9.90851e-05	0.00703795	intron-variant	NEBL	GRCh38.p7	10:20785939	CTGAGAAAGGAAGAA[A/G]GGATTATACGATGAA	10529
rs192194191	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21040542	TTTAAACAGCCAGCT[C/G]TCATGTGAACTAACA	10529
rs192197349	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21073416	GAGGTCAGGAGTTCA[A/G]GACCAACCTGGCCAA	10529
rs192200944	snp	A/G	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20809439	TTTCTACTGTTCTAT[A/G]TATAATTCTTTAAAT	10529
rs192201412	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:21165740	GTGTGGGCTCTTACT[C/G]CTGAGCTGAGACCTA	10529
rs192202786	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21104953	TGTTGCGCATAGTAA[A/G]ATGCTTTTCTACACC	10529
rs192209745	snp	C/T	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20983722	GGCCAACTGAGCAGC[C/T]CATTAGGCACAAACT	10529
rs192212385	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21001048	TCCCTCAGGAAACCA[A/G]TGCAGGTCCCCATGA	10529
rs192224565	snp	G/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20967694	GATAACAACTTTCAG[G/T]GGAGTGGTGACAAGA	10529
rs192226253	snp	A/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21036488	ATAAAGAATAAAAGC[A/T]TTGACAGTAGAAAGG	10529
rs192232919	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21051653	GAACAAATTAAGTCA[C/T]TCCCTAACAATAATC	10529
rs192238544	snp	C/T	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:21064872	GATCATAAAAAGCAA[C/T]CTGAGAAAGGAAATT	10529
rs192238820	snp	A/C	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21018510	CCAGTATACAAACAC[A/C]AGCATTTTACACAAA	10529
rs192255968	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20882990	TGTGGGAAGACACCC[A/G]TCACTGACTTCTGTT	10529
rs192268576	snp	A/C	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21095493	GTGCTATTAGCATAA[A/C]TGTACCTTTTAAAAC	10529
rs192271876	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20817823	TTACATCAACCTTCA[C/T]GCTTACATATACGCC	10529
rs192283559	snp	A/G	0.00993419	0.0697739	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20851547	TTGGGAGGCCAAGGC[A/G]GGCAGATCACAAGAT	10529
rs192283883	snp	C/G	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21127750	AAGGGAATTAAAAGG[C/G]GGAAAGGAGTGGAAG	10529
rs192315965	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20923948	ATCTAGCCCTTTTCT[A/G]ATTCATCTGGGTGTC	10529
rs192329445	snp	A/G	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20911497	TGAATGGCCAATAAA[A/G]TATAGGACATTTATA	10529
rs192341838	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21170471	TGGGTGCTTGGGGCC[C/G]TTTCCCTTCTCCTTA	10529
rs192347219	snp	A/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21041885	CGATGTTGTCATACA[A/T]TTGTAAACTGTCATG	10529
rs192358165	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21017043	GCTCTCTGAGCAAGG[A/G]GACCAGGGTACTGGT	10529
rs192370640	snp	A/C	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20983195	AAAATCAAATTAGAT[A/C]ATCTCCATAAGTCTT	10529
rs192370975	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20907694	TAAGTTTCACTGAAA[C/T]GAGATTTTCCTATTT	10529
rs192399917	snp	A/C	0.000798403	0.0199641	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20860523	GAAATATGAGAATGC[A/C]TGTCATAACTAATTA	10529
rs192400266	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21104639	TTTCAGATTCCCTAC[A/G]ATTATCCACATAGAC	10529
rs192405499	snp	A/G/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20879097	TCTTTCCTGCAGTGC[A/G/T]TTTGAAATCTGAAGA	10529
rs192408701	snp	C/T	0.00438332	0.0466095	intron-variant	NEBL	GRCh38.p7	10:20892996	CTGGAGGAGTAACCA[C/T]AGAATTTAATGTTTT	10529
rs192413373	snp	C/T	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:21067161	TATTTATAGTAGAGA[C/T]GGGGTTTCACCGTGT	10529
rs192413544	snp	A/C	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21141071	TCGACAAAAAAAAAA[A/C]AAACCTGCTCTATGC	10529
rs192415999	snp	C/G	0.00914312	0.0669923	intron-variant	NEBL	GRCh38.p7	10:21120292	AGATAGAAGGATTAC[C/G]TAAGCCTAGGAGGTC	10529
rs192418857	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21109805	GGTGTTTATAGTATT[C/T]TCTGATGGTAGTTTG	10529
rs192419006	snp	A/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20829685	AATTGTATTTCAGTG[A/T]TTAAAATCCCTTAAA	10529
rs192432034	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21155355	AATCACCTTGTTGTG[C/T]TATCAAATACCAGGT	10529
rs192438160	snp	A/T	0.00318978	0.0398085	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20846310	TAAATAAATTCTGCA[A/T]GAAATTGTTATTCAG	10529
rs192438970	snp	C/T	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20980555	TACAAACAGTGCAGG[C/T]AGCATGGAGGTGACC	10529
rs192454531	snp	A/C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20996598	ATTAAGTGGCGGAGA[A/C/T]AAATTGAAACCCAAG	10529
rs192463545	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20962325	AAGTTTTTATTCAAC[C/T]TCAGAAGGCCAACAT	10529
rs192469856	snp	A/G	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21145057	AAATAAAAGATGCTC[A/G]TGGATAGAACAAGAA	10529
rs192475655	snp	A/C	0.00597247	0.0543191	intron-variant	NEBL	GRCh38.p7	10:21048517	CACCACATGAGTTTT[A/C]AAAATATAAAAGTGG	10529
rs192481491	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21087434	TGCCTGTTGATATGT[A/G]CAGAATGCCACCTAG	10529
rs192486539	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21015905	TGTGTTCCAAAACTT[C/T]TGTTTCTAAGTCAGG	10529
rs192486713	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21058077	GCAATCAGCTCAGCA[C/T]GTTTTCTCAGAAATG	10529
rs192490605	snp	A/C	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:21034487	GGCACCTGTTGCCAG[A/C]CATCCTAGAGCACAG	10529
rs192491714	snp	C/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21073168	ACCCTGGAAAAATGT[C/G]TTCATTCATCAGGGC	10529
rs192513349	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20915389	TAGGTATATCTCCCA[A/G]TGCTATCCCTCCCCC	10529
rs192522612	snp	C/G	0.00478085	0.0486577	intron-variant	NEBL	GRCh38.p7	10:20893508	AAGCAGAAACTAGGT[C/G]GGGGGAGAAAGAGAA	10529
rs192526357	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20925505	TTCCCAAAGCGTCCA[C/T]CCTCCAAAAGCATGG	10529
rs192536946	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21053310	GTTAAGCAGACTTCT[G/T]GGCTATAATCCCACT	10529
rs192540546	snp	A/G	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:21085037	TGGTAGTGTCACTGG[A/G]CTTGTCACATTCACT	10529
rs192548003	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21070362	CCTGGTTAAAATTAA[C/T]GACAGATTAATGTAA	10529
rs192550242	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20896328	TCATTCAATAATTCT[A/G]GGATTCCCTTAAAGT	10529
rs192553071	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20957487	GATATTTGGGAAAGC[A/G]GACAGATAATTAAAA	10529
rs192565934	snp	C/T	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:20976563	AGAAAAGGTGCTACA[C/T]ATACACCATGGAATA	10529
rs192572887	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20956861	TAATTGCCTCATACA[C/T]GATAATTTTGCCACC	10529
rs192574842	snp	C/T	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:20940813	CTATAAACACCTCTA[C/T]GCAAATAAACTAGAA	10529
rs192584852	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21028990	AAGTGTTGCTTTCCC[A/G]CTCCCAACATGGCGG	10529
rs192591568	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21009796	AAGGTCCTTCTGAAG[A/C]TAATGGGTGCTCTAA	10529
rs192593114	snp	A/C	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20991462	TCATGGAAAAGATAA[A/C]ATTTTCCCTGATATT	10529
rs192602472	snp	A/C	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21058591	TTGTAAAAGAAACAA[A/C]ATTATTTAATGGCAT	10529
rs192606916	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20841939	GTAGATCCAAATGCC[C/T]TCTATGAATACTTAC	10529
rs192616503	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21088696	CACATTAGCAGCAAA[A/G]AATAGTGACAGCCAT	10529
rs192649287	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:20791605	TTGCTACATTGCCCA[A/T]CCTAGTCTCAAATTC	10529
rs192653600	snp	A/T	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	C10orf113, NEBL	GRCh38.p7	10:21146701	ACTGATGGAAAAGAA[A/T]TGCAATGCCCTGGTA	10529
rs192665216	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20866905	TACTGAGCCGTTAAT[C/T]TTTTTCATTCATGGT	10529
rs192665426	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21116721	GTCACTCAGGCTGGA[A/G]TGAAGTGGCACAATC	10529
rs192672180	snp	C/T	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:21116424	ATCATAAAGGCCCTA[C/T]TCTCATAACATCACC	10529
rs192673927	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20895618	CTTATTATTACTGCA[A/G]TTTACAGAGAACTTT	10529
rs192679524	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20992160	TTTCACTTTTTAAAA[A/G]TTACTTTGCTAATTA	10529
rs192679627	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21152786	AGACTAATGAGTCAA[A/G]CTGTAGTCCAGAAAT	10529
rs192682404	snp	A/C	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21017886	TAGAGTACAGTGGCA[A/C]GATCTCGGCTCACTG	10529
rs192697351	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20833786	GAAAAAAAGAATGTC[C/T]ACTAGGAAGGCAATA	10529
rs192708916	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20802125	AGGCAGGTAAACACC[A/T]GGTGAGATTGCAAGC	10529
rs192713138	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21066679	TTTGCTTAGATTTAC[A/C]ATTGCTTAAAACACA	10529
rs192719221	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21033899	GTCTGGGCACAGTGG[C/G]TCACGCTGGTACTCC	10529
rs192730850	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21096345	TAATACAATTTGCAT[A/G]TAAAACTCGCTTCTC	10529
rs192744430	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20996256	TTTTCCCCAGGGGGT[A/G]GGGCAAACTAACAAA	10529
rs192755630	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20809121	GGTATTCAATTCTAT[C/T]CACATCAAAAATTAA	10529
rs192758024	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20782633	TATTCCTACAAGGTG[C/T]TTGTGGAAACTGTGC	10529
rs192776294	snp	C/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20995515	ATTATGAGGGGATTT[C/G]CAGCAGCACCGCACG	10529
rs192778817	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21025532	ATAGGAAAAGTTATA[C/T]GCAAATCACTAGACC	10529
rs192787482	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21121199	GTTCAAAGAAGGAAA[C/T]GGTATTTCTTTCCAT	10529
rs192790628	snp	A/C	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20930269	GTTCTTGTTTTCCCT[A/C]CTCCCTCATTACAAA	10529
rs192798327	snp	A/C	0.0126979	0.078662	intron-variant	NEBL	GRCh38.p7	10:21156683	CTTGAAATACAGATA[A/C]AATCCTTCATTGCTT	10529
rs192807142	snp	C/T	0.00914312	0.0669923	intron-variant	NEBL	GRCh38.p7	10:20900767	GAAGAATCGCTTGAA[C/T]TTGGGAGGCGTAGGT	10529
rs192808148	snp	C/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20961536	GTTTACCAGATGAAA[C/T]TGGCATAGTCTATGC	10529
rs192809853	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21171608	TGGGGGTAATAATAG[C/T]GTCCCCTAACTCGTA	10529
rs192810405	snp	G/T	0.00119737	0.0244387	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20879338	GCATGGCTGTGCTCA[G/T]TAAGTGGTAGTTATT	10529
rs192828488	snp	A/G	0.00557542	0.0525036	intron-variant	NEBL	GRCh38.p7	10:20999659	CTATATCCAGGATCT[A/G]TATACCCAGGGTTGT	10529
rs192830191	snp	C/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21044110	AATGTTAAAAAGCCA[C/G]CATAGGCAGGGCACG	10529
rs192833564	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:20912851	TGCCATGCTGAACTT[C/G]TTCCTCATGGGGGCC	10529
rs192836185	snp	C/T	0.00478085	0.0486577	intron-variant	NEBL	GRCh38.p7	10:21101516	GGCAAGACCTAGAGA[C/T]GGTGGGGAAAAAAGA	10529
rs192837018	snp	A/C	0.0236746	0.106192	intron-variant	NEBL	GRCh38.p7	10:20941130	CTGGCAGAGACACAA[A/C]AAAAAAAGGGAATTT	10529
rs192844939	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21078511	CATCCTGAGTTTCAC[G/T]CCTGGTTAATACACT	10529
rs192850568	snp	A/G	0.00318978	0.0398085	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20883542	CAGAGGTAGGGAGAG[A/G]AGGAGTTTCATGGGT	10529
rs192853104	snp	C/T	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21137362	CCACAGCTATTCTTG[C/T]ATGCTTAGTCTTCAT	10529
rs192860044	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20856143	TCACAATTTGTCTAT[A/G]GGGAAAAAGAAATCT	10529
rs192866503	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20878967	AGCCTCCCGGGGATC[C/T]GTGTAACACCAGACC	10529
rs192868549	snp	A/G	0.00279162	0.0372561	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20854228	CCAGTAAAAATGGCA[A/G]TAGAGTGGAGGGATC	10529
rs192871326	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20937769	TTCCGACGGTTTTAG[C/T]AAACGGCACACCAGG	10529
rs192876559	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20907261	ATAAGTCTTCAGTGT[A/G]GAAATGTATTTTATT	10529
rs192880232	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21124420	ACCATTATAATCAGG[C/T]CTGGGCCTTTTTTCC	10529
rs192888200	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21161974	AAAAACCAACTCTGT[A/G]ATTAGAGGTTTGGGG	10529
rs192889805	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20821657	AGAACAATTTAATCA[C/T]GAAGTCAACTGCTCT	10529
rs192898140	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21035938	GAGGCTGAGGTGAGC[A/G]GATCACTTGAGGTCA	10529
rs192909557	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20856939	GTTTAAATGATTCTC[C/T]TGCCTCAGTCTCCTG	10529
rs192915211	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21047947	CAATGTTATTGCCAT[A/G]TAGCTTAGAACCTTC	10529
rs192927194	snp	G/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21081295	TTTGAGTTGTGGGGA[G/T]CTCCAGCAGCTGGCA	10529
rs192937215	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20801884	TAAACTGCTACAAAA[C/T]TCAGAAACTTACTTT	10529
rs192954694	snp	C/T	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:21015555	CTGTGTCAGCCAGGC[C/T]GCTGGAGCACAGTGG	10529
rs192961993	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20981207	CTAAAGATAGAGAAC[A/G]CATAAAGTTCAAAAT	10529
rs192966902	snp	A/G	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:20795237	GCAGTAGAAGTGAGA[A/G]AGAGGGAAAGGTAAA	10529
rs192969222	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:20825697	CAATGTACTAAATAT[A/T]CATGGGAGAATATCA	10529
rs192978800	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20918617	GCACTTTGGGAGGCC[A/G]ACGGGGGCAGATCAA	10529
rs192993284	snp	A/G	1.65064e-05	0.00287279	intron-variant, synonymous-codon, nc-transcript-variant	NEBL	GRCh38.p7	10:20889920	TGTACACTTATCCTT[A/G]GACTTTTTAAACTCT	10529
rs193000090	snp	C/G	0.00199481	0.0315187	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21142707	GTATGGCGAGCATTA[C/G]TGCTACTGCCTTCTG	10529
rs193014269	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21152374	CTCCCCACCTCCATT[G/T]CCCAAAGTTATACAA	10529
rs193014713	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20987322	GATGACCCCATTCCT[A/G]CCCATTGCTGCTTCC	10529
rs193026133	snp	A/C	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20952395	TGAGCCGAAATTGTA[A/C]CACTGCACTCCAGCC	10529
rs193040427	snp	A/G	0.00438332	0.0466095	intron-variant	NEBL	GRCh38.p7	10:21062525	AAAATAAAAAATAAA[A/G]ATAAAAATAAAATTA	10529
rs193042315	snp	C/G	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:21030578	CACAGCACGAATACC[C/G]TACAAGTGGTGGGGG	10529
rs193043740	snp	A/G	0.00318978	0.0398085	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20870871	TAGATCACATTCGTC[A/G]TTTAGATTAACTTGA	10529
rs193047300	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21084748	GAATGAATGAAATAA[A/C]CTTGCCTTCTCCCTC	10529
rs193048332	snp	C/T	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:21115810	TGTTCCTTCCCAATC[C/T]GCTCTTAATTTTTTA	10529
rs193062286	snp	C/G	0.00478085	0.0486577	intron-variant	NEBL	GRCh38.p7	10:20920919	TTGATGTATGATTAG[C/G]TCCATTTATTTCTAG	10529
rs193063864	snp	A/G	0.00557542	0.0525036	intron-variant	NEBL	GRCh38.p7	10:21082088	ATCCCTGCCAACCAT[A/G]CCTAACCTGAATATA	10529
rs193069602	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21110939	TCACAAGCATTCCTA[C/T]GCAGCAATAACAGAC	10529
rs193072400	snp	A/C	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20952309	GGGCGTGGTGCCAGG[A/C]ACCTGTAGTCCCAGC	10529
rs193074854	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21150041	TTAAGTTATGTTCCT[C/T]TTTTAGCATATTATT	10529
rs193076467	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20838008	ACCAAACAGTTCTGA[C/T]AGAAATGTATAAGGA	10529
rs193078976	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21024886	GCTGGTGGTCCTCAT[A/G]CGATTATAGAAGAGA	10529
rs193079542	snp	A/C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20892185	CAAGCTGATCTAAAC[A/C/T]AGGCATGGTCATGCC	10529
rs193085457	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20806242	GCTGCAGAGGGAGTA[A/G]AGGCATCCAAGCAGA	10529
rs193099807	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21037044	GACACCCCTGGCCAC[A/G]CACAGCACTTGTAGA	10529
rs193101903	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21001092	CTCCCTTCTCCACAG[A/G]AAGCAGCAGGTAAGA	10529
rs193103459	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21061743	TCCCTAAAAGTGGTT[A/G]TGACCTCCTCAGCCT	10529
rs193106940	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21091640	ATTATATTATTTGGG[G/T]GATGGGGGTCAGGGT	10529
rs193108619	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20860350	GTCAACTTAATGTCA[A/G]TGTAAAACTTTCTCT	10529
rs193109395	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21123768	ATATATTCATAAAAT[C/T]TTCAACATATATAAT	10529
rs193113693	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20933745	TCCATTTCAAAAACA[A/G]AAAAAGAAAGTTACA	10529
rs193121489	snp	A/G	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20968555	GAGGAGGGAGGAATC[A/G]TAGAAGTTCAAGGGG	10529
rs193128932	snp	C/T	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:20814350	TCTGTAATCACAGCA[C/T]TTTGGAAAGCTAAGG	10529
rs193130023	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20783465	TTTAGGAGACTTATT[C/G]CTCAAATATGTATTG	10529
rs193130804	snp	A/G	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20836656	GGCAGTTTGCAAGAG[A/G]GAGGAGCCTGGCCTC	10529
rs193135626	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20804914	TGGAGAACAGATCAG[A/G]GCAGGAGGTGGGTGG	10529
rs193155048	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20842284	TCTTTCATTTATTTC[A/G]TGGTGTGACCTTCGG	10529
rs193163659	snp	A/G	0.000395778	0.0140617	intron-variant, splice-donor-variant, downstream-variant-500B	NEBL	GRCh38.p7	10:20817596	GTTACTAAGATGATC[A/G]CACATTGCTGATGTT	10529
rs193168125	snp	A/G	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20788103	AACTCGGAATTCTAG[A/G]GAAGCCAACACAGAA	10529
rs193169767	snp	C/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21167543	GGTGAGAACACATTA[C/G]CTGGTCAGTCTTGGC	10529
rs193199527	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20876344	TTGTGTAGAAGGCAG[A/G]ATAAGTATTACTAAC	10529
rs193201490	snp	A/G	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:20933601	TAGCCGGGTGTGGTG[A/G]CACGTGCCTGTAATC	10529
rs193203241	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20904064	ACTAGTAATAAAATA[A/G]AATAATTATAACAAA	10529
rs193214275	snp	A/C	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20972783	AAAAAAATGTAAATG[A/C]ATTATACTTAGTGTG	10529
rs193224448	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20853498	ATGAACGAGATCCTG[A/C]CATTTGCAACAACAT	10529
rs193226446	snp	A/C	0.000399281	0.0141238	intron-variant, downstream-variant-500B	NEBL, LOC102725112	GRCh38.p7	10:20885184	CACAAATCTGATACT[A/C]TTTGGACACTGTAAA	10529
rs193233333	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21097446	GCTGGGCAACAGAGT[A/G]AGACTCTGTCCCCAA	10529
rs193240255	snp	C/G	0.0115144	0.0749975	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21129914	AATAATCACTTTGAA[C/G]ATCAGTGATCTAAAT	10529
rs193242681	snp	C/T	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:21040234	AGCTGGGTATGGTGG[C/T]GGGTGCCTGTAATCC	10529
rs193244992	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21004317	AAAGCCATTGAAATA[C/T]TGGAAAAATTTATTA	10529
rs193257421	snp	A/C	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21076879	AAGATAGACAAATGG[A/C]CAGAGACAGAAAGTA	10529
rs193257814	snp	A/G	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:21042979	TTCTTCAAAAATAAC[A/G]TTGCCCAAGAAATCA	10529
rs193258261	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21018900	GGGTGTGGTAGCAGG[C/T]GCCTGTAATCCCAGC	10529
rs193264836	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21106828	TATGAGCATGGAAAG[A/T]TCTTCCATTTGTTTG	10529
rs193274024	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20919079	AAATGCCTTAAGATG[A/C]AATATGATAATTAAA	10529
rs193275094	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20984175	GATTATATTAAAAAC[A/T]GGTACACCAAAAACA	10529
rs193277550	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20949527	AGATGAAGGAACCAC[A/G]GCCAGAGTTTCACTT	10529
rs193278372	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20820466	TGTCTTTTTAGACTT[C/T]AAAGCTCAGGTTAGG	10529
rs193283814	snp	C/T	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:20799396	CCTGGACTCTAGTGA[C/T]CCACCCACCTCCGCT	10529
rs193300740	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NEBL, NEBL-AS1	GRCh38.p7	10:21172834	AAAGGAATCCAGTTC[A/T]AAGTGTCTAAATGCA	10529
rs199498109	in-del	-/G	0.0279526	0.114869	intron-variant	NEBL	GRCh38.p7	10:21052440	GACTCCGGAGAGCCT[-/G]GCAGCAAAAGACACC	10529
rs199508774	in-del	-/GT			intron-variant	NEBL	GRCh38.p7	10:21097229	AGGTCCGGGGGGGGG[-/GT]GGGGCAGATCACAAG	10529
rs199523568	in-del	-/T			intron-variant	NEBL	GRCh38.p7	10:20836077	TTTGTAGATATTGCA[-/T]TTTTTTTTTACAAAC	10529
rs199526675	in-del	-/AAC			intron-variant	NEBL	GRCh38.p7	10:20980063	CCACAAAAAAAAAAA[-/AAC]AAACCATAAAATTCA	10529
rs199531054	snp	A/G/T	4.94295e-05	0.00497115	intron-variant	NEBL	GRCh38.p7	10:20897045	CTATTTGAAAAAAAA[A/G/T]AAAAGAACAGAAAGA	10529
rs199532962	snp	C/T	0.000599986	0.0173099	intron-variant	NEBL	GRCh38.p7	10:20812974	TCATACTGAATTTTG[C/T]GGATAGTTACCTCTT	10529
rs199549731	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20887233	TCAAAATGAGTTTAC[A/C]TGATGACAATTCTTA	10529
rs199567346	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20924968	ATCTGCAGACCCCCA[A/C]CCCCCTGCTCTATAC	10529
rs199572915	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20974268	TTTTTTTTTTTTTTT[C/T]TTTTAGACAGGGTCT	10529
rs199574432	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20943054	CAGGGATGTAGAACT[A/G]GAAATACCATTTGAC	10529
rs199584939	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21027311	ATCTTTAAAAAAAAA[A/C]CAACAACTTTTTTTG	10529
rs199587783	snp	G/T	0.000399281	0.0141238	intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20828539	ACTCACCGCACTAAT[G/T]TTTTGTTGAGTTGTC	10529
rs199591161	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20925751	AGCTATCAAGAGTAC[A/C]CAATTTGGAGTAGAG	10529
rs199606668	in-del	-/GTCCCCC			intron-variant	NEBL	GRCh38.p7	10:21029988	TGATAGACGTCCCCC[-/GTCCCCC]NNNNNNTCAAAGACC	10529
rs199620549	in-del	-/A			intron-variant, upstream-variant-2KB	NEBL, LOC102725112	GRCh38.p7	10:20844514	CCATTTAAAAAACAT[-/A]AAAAAAAAAAAGCTT	10529
rs199626535	in-del	-/TT	0.158302	0.232576	intron-variant	NEBL	GRCh38.p7	10:20942794	GATATGAATAGACAC[-/TT]CTCAAAAGAAGACAT	10529
rs199628586	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21122002	GTGGGGATTTCTCCT[G/T]GTTGTTGTTGTTGTT	10529
rs199650195	in-del	-/AGAACGT			intron-variant	NEBL	GRCh38.p7	10:20982377	TATTTTTTTATTTGT[-/AGAACGT]TGAACTTGAGCAAGA	10529
rs199661276	in-del	-/GT/TG			intron-variant	NEBL	GRCh38.p7	10:20795561	TGTGTGTGTGTGTGT[-/GT/TG]ATGTCAGATTAATTT	10529
rs199667295	in-del	-/AT	0.0126979	0.078662	intron-variant	NEBL	GRCh38.p7	10:21061438	ATTGCATGGTGTATG[-/AT]ATATATCGTATATTA	10529
rs199680310	in-del	-/A	0.0138799	0.0821421	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20853632	AGTTCTACAAAAAAT[-/A]AAGAAATCAGCTGGG	10529
rs199703128	snp	A/G/T	0.0111196	0.0737302	intron-variant	NEBL	GRCh38.p7	10:20814446	CTACAGGTAAAAATT[A/G/T]AAAAAAAAAAAAAAT	10529
rs199710101	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21168875	AACATGGTGAAACCC[C/T]ATCTCTACTAAAAAA	10529
rs199754613	snp	A/T	0.0023933	0.0345097	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20876947	CGATTGGCTGTTTTT[A/T]ATCATTTTCTGATTA	10529
rs199805565	snp	A/G	0.104149	0.203046	intron-variant	NEBL	GRCh38.p7	10:21028251	AAAAAAAAAAAAAAA[A/G]AAAAAGAAGAAGAAG	10529
rs199814224	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21105568	ATATGTGCCACATTT[C/T]CTTAATCCAGTCTAT	10529
rs199817316	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21054719	ATGCCAAGCTCTGCC[C/T]GAGATCCCTATTAAT	10529
rs199821922	snp	A/C	1.65452e-05	0.00287616	intron-variant, synonymous-codon, nc-transcript-variant	NEBL	GRCh38.p7	10:20809888	AGGATCTGTGCGCCA[A/C]ACTTTGAGGTCTTTT	10529
rs199822950	in-del	-/T			intron-variant	NEBL	GRCh38.p7	10:21002165	AGGGTTTTTTTTTTT[-/T]ATGGTGATGAAACAT	10529
rs199826867	in-del	-/CA			intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20960711	ATACACACACACACA[-/CA]TATATACATGTATAC	10529
rs199827353	snp	G/T	0.00438332	0.0466095	intron-variant	NEBL	GRCh38.p7	10:21112254	GGTATATACCCAAAG[G/T]ATTATAAATCATGCT	10529
rs199827432	in-del	-/TTATTTATTTATTTAT			intron-variant	NEBL	GRCh38.p7	10:21034944	ACTAGCTATTTATTC[-/TTATTTATTTATTTAT]TTATTTATTTATTTA	10529
rs199848081	in-del	-/T	0.0502101	0.15028	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20862874	ACCTTTTTTTATTAA[-/T]TTTTTTTTATTTTTA	10529
rs199853597	snp	A/T	0.32885	0.23724	intron-variant	NEBL	GRCh38.p7	10:20803818	TGTACGAAAAATATA[A/T]ATATATATATATATA	10529
rs199860020	snp	C/T	0.000115772	0.00760741	intron-variant	NEBL	GRCh38.p7	10:20785963	CGATGAATGCCGAAA[C/T]AGCTACAGCCACAAA	10529
rs199866448	in-del	-/AAGGGAAGGG			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21137939	AAAAAAAAAAAAGGA[-/AAGGGAAGGG]AAGGGAAGGGAAGGG	10529
rs199870607	snp	C/T	1.81371e-05	0.00301135	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20859672	AAAAAAAACAAGAAT[C/T]AAAAGATTTTGAAAA	10529
rs199877830	in-del	-/AAGGGA	0.0142736	0.0832652	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20882352	GAAAAGGAAAAGGGG[-/AAGGGA]AAGGGAAAGGGAAAG	10529
rs199882043	snp	A/C			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21141060	ACAAGAGGTATTCGA[A/C]AAAAAAAAAAAAAAC	10529
rs199887353	snp	A/G	0.000235339	0.010845	synonymous-codon, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20787295	TTGCTGATAGGCTCC[A/G]GGAAGAACAGGTGCT	10529
rs199919350	snp	C/T	0.00478085	0.0486577	intron-variant	NEBL	GRCh38.p7	10:21000059	CTTTCACTGCTGCCA[C/T]GAACTATTGTAGTTT	10529
rs199926622	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:20967628	GCGAGACTCCATCTC[-/A]AAAAAAAAAAAACAA	10529
rs199928134	in-del	-/T			intron-variant	NEBL	GRCh38.p7	10:20803814	CTTCTGTACGAAAAA[-/T]ATATATATATATATA	10529
rs199935965	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:20888234	AAAAACAGGAAAAAA[A/T]TAAATAAATAAACTT	10529
rs199936271	snp	C/T			intron-variant, synonymous-codon, nc-transcript-variant	NEBL	GRCh38.p7	10:20897146	TTCTTCATTTTCTTC[C/T]TCCCCTATCTTTTCT	10529
rs199938692	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21020535	TCATCCATCCTCCAA[A/C]CAAACTTCCTGACAA	10529
rs199947337	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:20999160	CAGAGGTGTGTGGGG[-/A]GGAAAAAAAAAAAAA	10529
rs199955302	in-del	-/A			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21127563	TAGAAAAAAAAAAAA[-/A]GAAAATTTGAGCCAG	10529
rs199964725	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:20980343	CAGAACAAAAAGAAC[-/A]AAAAAAAAAAGTTTC	10529
rs199978424	snp	A/C	1.65496e-05	0.00287655	intron-variant, downstream-variant-500B	NEBL	GRCh38.p7	10:20815583	AGTAAATAATAAAAG[A/C]CACATCCTTTGTGAT	10529
rs200000605	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21113308	AAAAAAAAAAAAAAC[G/T]AGGAAAAAACTCCTA	10529
rs200028536	in-del	-/C	0.0189856	0.0955633	intron-variant	NEBL	GRCh38.p7	10:20909292	ACCTCCCCACCACCA[-/C]CCCCCACTACCCTTT	10529
rs200030299	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:20829725	TTCTCACACCACACT[-/A]AAAAAAAAATCTATG	10529
rs200064013	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21089847	AACAGATGGGTTTTC[A/C]AAAAACATGTCCATA	10529
rs200080784	snp	C/T	0.000214736	0.0103596	intron-variant	NEBL	GRCh38.p7	10:20785946	AGGAAGAAGGGATTA[C/T]ACGATGAATGCCGAA	10529
rs200086494	in-del	-/ACTG	0.0425829	0.139564	intron-variant	NEBL	GRCh38.p7	10:20946967	CCAAGATCCCCAGAA[-/ACTG]ACTGACTCCAAAGAA	10529
rs200093504	in-del	-/T	0.0244538	0.107838	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20874741	CCATTTCACTTTTCA[-/T]TTTTTTTTCTTTTTT	10529
rs200103473	in-del	-/A	0.0182019	0.0936463	intron-variant	NEBL	GRCh38.p7	10:20994882	TGAGGAGGAGGAGGT[-/A]GAGGGGGGGGTTGGT	10529
rs200103716	in-del	-/A	0.0217236	0.101931	intron-variant	NEBL	GRCh38.p7	10:20901584	GTTCTGAGTGGGGGG[-/A]AAAAAGTACAGAGAT	10529
rs200137869	in-del	-/G			intron-variant	NEBL	GRCh38.p7	10:21034180	CGAAAAAAAAAAAAA[-/G]AAAAAAAAAAGACCC	10529
rs200162351	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20925706	GAATTCCAGAGAGAA[A/C]AACAATTAAAAAAAA	10529
rs200168071	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21029700	TTCAGACCAGTCTGG[A/C]CGTGGGTATTGGTAT	10529
rs200170545	in-del	-/TT			intron-variant	NEBL	GRCh38.p7	10:21074484	TTCTGAATTTTTTTC[-/TT]TTTTTTTTTTTTGAG	10529
rs200177229	snp	C/T	1.66532e-05	0.00288554	intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20831576	TCCAGATCTCTTTTA[C/T]AGTCTTTCTGCAGAA	10529
rs200196192	snp	C/T	0.00199791	0.0315431	intron-variant, upstream-variant-2KB	NEBL, NEBL-AS1	GRCh38.p7	10:21173726	AGGTGCAGCCCCTCG[C/T]CCGGCAGGTCCAGGC	10529
rs200196436	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21093167	TTTTTTTTTTTTTTC[C/T]ATTTTAGCAGAGCCA	10529
rs200209859	in-del	-/GCGCAAGCCC			intron-variant	NEBL	GRCh38.p7	10:20814314	CTAGTCTGTAAACCT[-/GCGCAAGCCC]GAGGACTCGTATCTG	10529
rs200215327	in-del	-/T			intron-variant	NEBL	GRCh38.p7	10:20974253	TTTTTTTTTTTTTTT[-/T]CTTTTAGACAGGGTC	10529
rs200216162	snp	A/T	1.64955e-05	0.00287184	intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20831512	CTTAGCTCTCTGGAC[A/T]TCAAGAGTGTCTGTG	10529
rs200226086	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20941261	GTGGGCTTCATCCCT[A/G]GGATGCAAGGCCGGT	10529
rs200226181	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20923697	AAAAAAAAAAAAAAA[C/T]AAATGGTTTCTTGAC	10529
rs200226331	in-del	-/TG			intron-variant	NEBL	GRCh38.p7	10:21010434	ATTTTTTTTTTTTTT[-/TG]CAAGAACAGGGTTTT	10529
rs200226927	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:21058562	GTTTTGTAGTGTATT[-/A]AAAAAAAAACAACTT	10529
rs200231082	snp	A/G	0.000307449	0.0123947	intron-variant	NEBL	GRCh38.p7	10:20840856	ATATTCTTTCTATGA[A/G]ACAAGAATATCACAG	10529
rs200249470	snp	C/T	0.00039672	0.0140785	intron-variant	NEBL	GRCh38.p7	10:20888092	ACACTTTAGAAAAAC[C/T]CTACCTCACTCTGGA	10529
rs200252670	in-del	-/A	0.0926964	0.194308	intron-variant	NEBL	GRCh38.p7	10:21036163	CTGGAGTCTCAAAAG[-/A]AAAAAAGAAAGAAAA	10529
rs200269733	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20916667	CACCCACCTCAGCCT[C/T]TCAAAATGCTGGGAT	10529
rs200273688	in-del	-/A	0.00914312	0.0669923	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20859235	ACACAGAATGAAAAC[-/A]AATCACATAAGGAAG	10529
rs200283864	snp	A/C	0.00213631	0.0326127	intron-variant	NEBL	GRCh38.p7	10:21020247	TAAAATATTGTGCTA[A/C]AAAACAACACTTTCA	10529
rs200289094	in-del	-/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20868050	ATCATTTTATCTATA[-/T]TTAAAAAAAAAAAAA	10529
rs200298839	in-del	-/ATT			intron-variant	NEBL	GRCh38.p7	10:20886029	CATTTTTCAAGAGTA[-/ATT]ATGTATTTTCAGACT	10529
rs200302319	snp	A/C	0.0329836	0.124112	intron-variant	NEBL	GRCh38.p7	10:20814599	AGAGACTGTGTCTCA[A/C]ACACACACATACACA	10529
rs200311632	in-del	-/A	0.00716266	0.059414	intron-variant	NEBL	GRCh38.p7	10:20790317	TCCTATAGGGGTTAT[-/A]AAAAAAAATAACTGA	10529
rs200317527	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21118115	CTGGTGCAGCACCCC[G/T]CAGCCACTACCAATG	10529
rs200334335	snp	C/T	3.30153e-05	0.00406283	intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20813975	TTCTTTAACATGTCT[C/T]ATAGCAGGTGTATCT	10529
rs200339723	snp	A/T			missense, intron-variant	C10orf113, NEBL	GRCh38.p7	10:21146413	TAGTAAAGCACAAAC[A/T]CTCTCTCTCATATAA	10529
rs200356473	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20888049	GTAGCTTTTTTCCAG[C/T]TATATGTTTTATCTA	10529
rs200391286	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21102638	ATTCTTTTGAGAGTC[A/G]TTAAATATATTGATA	10529
rs200398022	snp	A/G	8.45044e-05	0.00649962	intron-variant	NEBL	GRCh38.p7	10:20808703	GTGATTAAGTGACTC[A/G]AAAAACAAAATCAAC	10529
rs200406220	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20984125	ACAGAAAATGTACCT[A/G]AAAAAAAAAAAGCTC	10529
rs200423872	in-del	-/C	0.0221141	0.102801	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21146072	GCTATGAGCCAGGCA[-/C]CCATGAATAGGGAAA	10529
rs200449537	in-del	-/TAA			intron-variant	NEBL	GRCh38.p7	10:21092587	TTTACCTCTATAATT[-/TAA]TAATAATAATAATAA	10529
rs200473083	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21053482	CTTCTTCTTTATTGC[C/T]TTATGTTGTTTAAAC	10529
rs200485102	in-del	-/AC	0.202343	0.245416	intron-variant	NEBL	GRCh38.p7	10:20980064	CACAAAAAAAAAAAA[-/AC]AAACCATAAAATTCA	10529
rs200491365	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20982375	TCCTATTTTTTTATT[C/T]GTTGAACTTGAGCAA	10529
rs200503254	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20955911	CCTCATCTCTTGTTT[A/C]AAAAAAAAAAAAAAG	10529
rs200507639	in-del	-/AG			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20860566	AAGTTCACTACAAAA[-/AG]AAAAAAAAAAAAAAA	10529
rs200513864	in-del	-/T	0.0391387	0.134304	intron-variant	NEBL	GRCh38.p7	10:20814443	CTCTACAGGTAAAAA[-/T]TTAAAAAAAAAAAAA	10529
rs200516044	in-del	-/T	0.0205511	0.0992634	intron-variant	NEBL	GRCh38.p7	10:21114492	CTGATTTTCTGTCTA[-/T]TTGTTCTACCAATTA	10529
rs200534792	snp	C/T	1.65776e-05	0.00287898	intron-variant, missense, nc-transcript-variant, upstream-variant-2KB	NEBL, LOC102725112	GRCh38.p7	10:20845278	TCAGAAGGTTGGTGA[C/T]GTACTTTACATGTAA	10529
rs200562329	snp	A/C/G/T	0.000136798	0.00826941	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20850535	AAGCATATACAAATC[A/C/G/T]AAAGTCCTTATACAA	10529
rs200571909	in-del	-/A	0.47937	0.144001	intron-variant	NEBL	GRCh38.p7	10:20809950	AAAAAAAAAAAAAAA[-/A]GCCAGTACCCAAAAG	10529
rs200574474	snp	C/T	0.000363811	0.0134823	intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20813941	GGTTGGACCCTACCA[C/T]TGAAATATGATTTTG	10529
rs200612536	snp	A/G	0.350546	0.22889	intron-variant	NEBL	GRCh38.p7	10:20809950	AGGAATTTAAAAAAG[A/G]AAAAAAAAAAAAAAA	10529
rs200616626	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21016049	TTTTACTTTTGCTTC[G/T]TGTTGAATGGGCTGC	10529
rs200622730	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20918955	AAACATTATGCATAG[A/G]AAAATTCTGGAAGGA	10529
rs200626913	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21027326	ACAACAACTTTTTTT[G/T]TTTTTTTTTTTTTAA	10529
rs200626940	in-del	-/A	0.132751	0.2208	intron-variant	NEBL	GRCh38.p7	10:20829455	GTAGGGGGAGGGGGG[-/A]GGGATAGCATTAGGA	10529
rs200629477	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:20980225	ATCACCTATAAAACT[C/G]AAATGTCATCAGTGA	10529
rs200638590	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20926406	TATGTGAAATTTTGC[C/T]TCTTTTATGATCTCA	10529
rs200642113	in-del	-/AAAAAAA	0.318896	0.240319	intron-variant	NEBL	GRCh38.p7	10:20954026	AAACTCTTCTTAAGG[-/AAAAAAA]AAAAAAAAAAAGAAA	10529
rs200655561	snp	A/G			intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20826449	GTAGAGAACTTACTG[A/G]ACTAATATTCTGCTG	10529
rs200664378	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20904045	ATGTCATAGCAAGAG[A/G]ACAACTAGTAATAAA	10529
rs200672631	in-del	-/T			intron-variant	NEBL	GRCh38.p7	10:20886188	AGAACTTAAAAAAAA[-/T]TTTTTTTAATAAGAT	10529
rs200674866	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21035325	ATTCTGATGCTCTCC[C/T]TCCCCCCGCCCCCCA	10529
rs200705273	snp	A/G	0.00016497	0.00908063	missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20812870	TTCCTCACTCTCTCT[A/G]TCACAGGATCGTCCA	10529
rs200712707	in-del	-/A	0.00478085	0.0486577	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20898172	CGTAAAACCAAGGTT[-/A]AAAAAAAATTTCTCA	10529
rs200731667	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20952564	TGTAGAAGTTTTCCT[A/G]GAAAGGCAACAGGTA	10529
rs200732375	snp	A/C	0.00199795	0.0315434	intron-variant	NEBL	GRCh38.p7	10:20896947	AGACAAAAATTACTC[A/C]AGCCACTTACATCGC	10529
rs200735943	snp	A/C/T			intron-variant	NEBL	GRCh38.p7	10:20976630	TGCAGCCACATGGAT[A/C/T]GAGCTAGAGGCCATT	10529
rs200756166	snp	G/T	0.000902271	0.0212208	intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20823216	TGATCACATTGCTGA[G/T]GTTCTTCTGGTTTTC	10529
rs200757731	snp	A/G	4.94588e-05	0.00497262	intron-variant	NEBL	GRCh38.p7	10:20897095	TTTAGAGGAACAAAC[A/G]CTGGTCTGAGTATGT	10529
rs200763746	in-del	-/AC			intron-variant	NEBL	GRCh38.p7	10:20981413	CATCTCATAAAAAAA[-/AC]ACACACAAAATTATA	10529
rs200769319	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:20939603	TAACCTTAAACGTAA[A/T]TGGGCTAAATGCTCC	10529
rs200786173	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:20910841	TTGTTTTTTTTTTTT[G/T]GGCCAAAGGGGGATA	10529
rs200799762	snp	A/G	9.93756e-05	0.00704826	intron-variant, synonymous-codon, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20858240	AGATGAACCACTTAC[A/G]CCGCTGAGCATTTTG	10529
rs200814296	in-del	-/TTTT			intron-variant	NEBL	GRCh38.p7	10:21003004	TTTTCATTATGTGGC[-/TTTT]TTTTTTTTTTTTTTT	10529
rs200817547	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21152583	CTGTCCAAGAAAAAA[A/G]AAAAAAAAAAAATCC	10529
rs200817651	in-del	-/ACACAC			intron-variant	NEBL	GRCh38.p7	10:20963004	AAGCTTGAAAGAAAA[-/ACACAC]ACACACACACACACA	10529
rs200829162	snp	C/G	0.00199808	0.0315444	missense, upstream-variant-2KB	NEBL	GRCh38.p7	10:20961758	TCCCTTTGCTTTCTT[C/G]AAAATCTCTTTTGTA	10529
rs200834300	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21071814	AGTGTTGGGCTTTTT[G/T]TTTTTGATTTTGTCT	10529
rs200845615	in-del	-/AATA	0.0189856	0.0955633	intron-variant	NEBL	GRCh38.p7	10:20788433	GTGTTATGAATAATT[-/AATA]TTTTATAAGTAGAAA	10529
rs200858512	snp	A/G	6.6107e-05	0.00574884	intron-variant	NEBL	GRCh38.p7	10:20785949	AAGAAGGGATTATAC[A/G]ATGAATGCCGAAATA	10529
rs200862098	snp	C/T	0.000399281	0.0141238	intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20897029	CAGGCTTATAGAAGA[C/T]CTATTTGAAAAAAAA	10529
rs200866842	in-del	-/C			intron-variant	NEBL	GRCh38.p7	10:21024819	ACTCCACCTCTCCAG[-/C]AAAAAAAGAAAAAGA	10529
rs200875519	snp	A/G	3.29799e-05	0.00406065	intron-variant, missense, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20868737	GCGGGCTCTTTATTC[A/G]TTATTCCTTGTCCTT	10529
rs200877802	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21166246	AAAAAAAAAAAAAAA[A/G]AAAAGAAAAAAAAAT	10529
rs200879496	in-del	-/A			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20868231	TTTCTTCATTTTCAT[-/A]CTCCCTTTTTAAATT	10529
rs200885528	snp	A/C	0.306431	0.243548	intron-variant	NEBL	GRCh38.p7	10:21119452	ATATATAGTTATATT[A/C]ATATACTGAATATAA	10529
rs200888715	in-del	-/A	0.162253	0.234095	intron-variant	NEBL	GRCh38.p7	10:20829599	AATAATAATAAAATT[-/A]AAAAAAAAGAAAGGT	10529
rs200895451	in-del	-/G			intron-variant	NEBL	GRCh38.p7	10:20910833	TTCGTTTTTGTTTTT[-/G]TTTTTTTTGGCCAAA	10529
rs200898095	in-del	-/C			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20855525	GAAAACAAAACAAAA[-/C]AAAAAAAAAACGAAG	10529
rs200900765	in-del	-/AAAAAAAAAAAAG	0.478271	0.101943	intron-variant	NEBL	GRCh38.p7	10:21171338	AAACTTCTGTCTCAA[-/AAAAAAAAAAAAG]AAAAAAAAAAAAGAA	10529
rs200906180	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:21034974	TTTATTTATTTATTT[-/A]TTTATTTATTTATTT	10529
rs200929034	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:20888235	AAAACAGGAAAAAAA[A/T]AAATAAATAAACTTC	10529
rs200931116	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21028897	ATACTTGCCAGCTAA[A/T]AGATTGATATTGTCA	10529
rs200934881	snp	A/G	0.000150194	0.00866455	intron-variant	NEBL	GRCh38.p7	10:20808670	CTTTTCTATATTGGA[A/G]GGAAAATATTTACAC	10529
rs200966379	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20909149	TCGTTTGAGTTACAA[A/C]CATCCAACTACACTC	10529
rs200968845	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:20812327	GGAACATTCTTTTTT[A/T]TATTATTATTATACT	10529
rs200969342	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20800716	AGGTTGCGATATTTG[A/G]AAAAAAAAATCTACC	10529
rs200986422	in-del	-/TC			intron-variant	NEBL	GRCh38.p7	10:20903740	GGAGATGGAGGCCAT[-/TC]TATTCTAAGTGAAGT	10529
rs201001925	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21093168	TTTTTTTTTTTTTCC[A/T]TTTTAGCAGAGCCAA	10529
rs201002855	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:20968355	TAAAAAAAAAAAAAA[A/T]TTAAAATCAGCCAGG	10529
rs201003683	in-del	-/C			intron-variant	NEBL	GRCh38.p7	10:20926408	TGTGAAATTTTGCTT[-/C]TTTTATGATCTCATT	10529
rs201005969	in-del	-/TT	0.36955	0.219562	intron-variant	NEBL	GRCh38.p7	10:21010420	CAGCGAATTTTTTAA[-/TT]TTTTTTTTTTTTTGC	10529
rs201009353	in-del	-/T			intron-variant	NEBL	GRCh38.p7	10:20803816	TCTGTACGAAAAATA[-/T]ATATATATATATATA	10529
rs201040667	in-del	-/AAA	0.39527	0.203462	intron-variant	NEBL	GRCh38.p7	10:20969470	GGGGTTCTTTTACTT[-/AAA]AAAAAAAAAATGAAA	10529
rs201043505	snp	G/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20818304	TTTACTAGCTGGGTG[G/T]GGGGGCTGGGGGTGG	10529
rs201065598	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21033354	TACCTATAGCAAATG[C/T]GCAATATGAACAAAA	10529
rs201072548	snp	A/G	1.65886e-05	0.00287993	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20961798	ACAAGAAGGGGGAAA[A/G]GAAAAGTGAACAGAG	10529
rs201086392	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21101002	TTTGTGGCTTTTTTT[A/C]GAAGGAAATACTCAC	10529
rs201087707	in-del	-/C			intron-variant	NEBL	GRCh38.p7	10:21084593	GGAGCAAGACTCTGT[-/C]CCCAAAAAAAAAATA	10529
rs201098393	in-del	-/CTT	0.0107246	0.0724382	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20883603	CTATGAGATTTGCTC[-/CTT]CTTCTTAAATGAAAA	10529
rs201100655	in-del	-/G			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21130121	TTTCAAAACAGGGTA[-/G]AACTTCAAAACAGGG	10529
rs201103536	snp	A/C	0.000110233	0.00742324	intron-variant, stop-gained, nc-transcript-variant	NEBL	GRCh38.p7	10:20840822	CTTTCCCTTTTATCT[A/C]ATTTTCCAAATCTTT	10529
rs201105598	snp	A/G	0.000164932	0.00907958	utr-variant-3-prime, synonymous-codon, nc-transcript-variant	NEBL	GRCh38.p7	10:20785849	AGGCTGCACGTTGAC[A/G]ATGTAGTCGCCGTCT	10529
rs201107989	in-del	-/TTATTTAT			intron-variant	NEBL	GRCh38.p7	10:21034944	ACTAGCTATTTATTC[-/TTATTTAT]TTATTTATTTATTTA	10529
rs201136473	snp	C/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20878400	CATTTATAGCCATAG[C/T]GCAAAGTGACAGTCT	10529
rs201140394	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21026332	TACAGTACACTGTAC[A/G]GCCCCTCCCTGACAG	10529
rs201141089	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20952440	AGACTCTGTCTGAAG[A/G]AAAAAAAAAAAAAAA	10529
rs201143845	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21027339	TTGTTTTTTTTTTTT[A/T]AATTTTCAGATAGAG	10529
rs201150512	in-del	-/A	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:21028776	AACTCAATATAATTT[-/A]AAAAAAAAAATGAAG	10529
rs201152066	snp	G/T	1.6473e-05	0.00286988	intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20896999	TGGCCAATTCCATGC[G/T]TAAGTCTTCAATAAC	10529
rs201159572	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21015197	TCTACAGAAGACCAG[A/G]TTTCCTTAAGGCTCT	10529
rs201168676	in-del	-/A	0.0240643	0.107019	intron-variant	NEBL	GRCh38.p7	10:20953728	TTATCAAGCAGCACC[-/A]AAAAAGAAAAGAATC	10529
rs201170874	in-del	-/TTTTTT			intron-variant	NEBL	GRCh38.p7	10:21003004	TTTTCATTATGTGGC[-/TTTTTT]TTTTTTTTTTTTTTC	10529
rs201197235	snp	C/T	0.000362958	0.0134665	intron-variant, missense, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20880901	GTTTCTGCTTGTAGG[C/T]CACCTGAAAAACACA	10529
rs201210624	snp	C/T	1.64814e-05	0.00287061	intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20817665	CAGAAATTGCAGTTC[C/T]CCGTTGAAGTTCTCC	10529
rs201228873	in-del	-/T			intron-variant	NEBL	GRCh38.p7	10:20976920	ATTCCTGAATCTACA[-/T]TTAAAAAAAAAAAAA	10529
rs201233176	snp	C/T	0.00119737	0.0244387	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21125436	AGAAATGGGAAGTTG[C/T]GGAGGGGACTACTTA	10529
rs201238723	snp	A/C/G	0.000132106	0.00812639	missense, intron-variant, utr-variant-3-prime	C10orf113, NEBL	GRCh38.p7	10:21126034	AGCCACCTGGCAAGC[A/C/G]TTGGCCAGCTTTGCA	10529
rs201256382	snp	A/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20868052	TCATTTTATCTATAT[A/T]AAAAAAAAAAAAAAA	10529
rs201266355	in-del	-/A	0.0360663	0.129354	intron-variant	NEBL	GRCh38.p7	10:20812326	GGAACATTCTTTTTT[-/A]TTATTATTATTATAC	10529
rs201286912	in-del	-/AA			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21142920	CCTGTCCCTGGTGCC[-/AA]AAAGGTTGGGGATGG	10529
rs201293038	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20992240	CATTTTTTATGTTTT[A/G]TGACTATCTAGCATC	10529
rs201293813	in-del	-/TC			intron-variant	NEBL	GRCh38.p7	10:21123740	ATATATATATATATA[-/TC]ATCTCAAACTAATAT	10529
rs201296063	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20940262	AGTGCAATCAAACTA[A/G]AACTCAGGATTAAGA	10529
rs201314802	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:20919977	AAATTGAGAAAAAAA[A/T]TCAACAACCCAATAT	10529
rs201321150	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20828768	GACTTACACTCCCAG[A/G]GAGAGAGAGAGAGAG	10529
rs201325130	snp	A/G	0.000510645	0.0159707	intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20835523	CTAACCTCACTCGCT[A/G]TCTCTGCAGCCTTCT	10529
rs201351208	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21171349	TCAAAAAAAAAAAAA[A/G]GAAAAAAAAAAAAGA	10529
rs201379770	snp	A/C			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21130318	TTGGAAATTTCAACA[A/C]CCCTCTATCAGTACC	10529
rs201389478	snp	G/T	1.65002e-05	0.00287225	synonymous-codon, nc-transcript-variant	NEBL	GRCh38.p7	10:20812827	GTGGACCCCTTTATA[G/T]GCAGCATCGCTGACC	10529
rs201423708	snp	C/T	0.00199798	0.0315436	intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20896987	CCGTGCATTTTCTGG[C/T]CAATTCCATGCTTAA	10529
rs201427520	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:20982378	TATTTTTTTATTTGT[A/T]GAACTTGAGCAAGAA	10529
rs201428884	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21066824	TCTTACATTGTTCTG[A/G]GGTTTTTCTATTTAA	10529
rs201430201	in-del	-/AC			intron-variant	NEBL	GRCh38.p7	10:20829557	TAACCTGCACATTGT[-/AC]ACATGTACCCTGAAA	10529
rs201465578	in-del	-/A	0.199138	0.244771	intron-variant	NEBL	GRCh38.p7	10:20967184	AAAGAAAAAAAAAAA[-/A]TAGGAAACAACCTAA	10529
rs201470697	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:20978431	AACCAAAAAAAAAAA[-/A]CGAGTTATTTGATTA	10529
rs201482759	in-del	-/T	0.0111196	0.0737302	intron-variant	NEBL	GRCh38.p7	10:21069645	AAATCTTTATGTAGA[-/T]TTTTCTCACAAACTG	10529
rs201497107	snp	C/T	1.64751e-05	0.00287007	intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20819428	AAACGACTTGCCGCA[C/T]TCAGCTGCTCCTGGT	10529
rs201505742	in-del	-/T	0.0205511	0.0992634	intron-variant	NEBL	GRCh38.p7	10:21060558	AATATTTTCCCCCTC[-/T]ACTGGCTCATATATT	10529
rs201507270	snp	G/T			utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20785480	TTTCCCAGAAGGGTT[G/T]AATAGCCAATCAAAG	10529
rs201509611	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21027340	TGTTTTTTTTTTTTT[A/T]ATTTTCAGATAGAGT	10529
rs201511267	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21160402	TAACTGCTGTTTTAA[A/G]AAAAGACCACAGAGG	10529
rs201513089	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21035327	TCTGATGCTCTCCTT[C/T]CCCCCGCCCCCCAAA	10529
rs201513177	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21012901	AACTTTCCAGGCCTT[A/G]GGAAACAGATGAAAA	10529
rs201526111	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:20968341	AAGGCCCCATCTCTT[-/A]AAAAAAAAAAAAAAT	10529
rs201528218	in-del	-/T	0.0111196	0.0737302	intron-variant	NEBL	GRCh38.p7	10:21028773	TCTAACTCAATATAA[-/T]TTAAAAAAAAAAATG	10529
rs201528940	snp	G/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20875614	TAAACCAGAGAAAAG[G/T]AAAACCTCCACAGAC	10529
rs201530011	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:20904047	GTCATAGCAAGAGAA[C/G]AACTAGTAATAAAAT	10529
rs201534265	in-del	-/G			intron-variant	NEBL	GRCh38.p7	10:21103740	TTCTCTGGCTCCCTA[-/G]GTCATGACATGCGAT	10529
rs201539771	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21024827	TCTCCAGCAAAAAAA[C/T]AAAAAGAAAAGAAAA	10529
rs201553643	snp	A/G	0.000399281	0.0141238	intron-variant, missense, nc-transcript-variant, upstream-variant-2KB	NEBL, LOC102725112	GRCh38.p7	10:20845337	GATGACCTTCCTTTA[A/G]TCTCCTTCTCAAAAT	10529
rs201558941	in-del	-/A	0.0379877	0.132479	intron-variant	NEBL	GRCh38.p7	10:21104552	CCAGTACATAGAAAT[-/A]GCAAATGATTTTTAT	10529
rs201562096	snp	A/G	0.239037	0.24976	intron-variant	NEBL	GRCh38.p7	10:21160865	CTTATTTCCAGGGGG[A/G]AAAAAAAAAAAAACA	10529
rs201571938	snp	C/T	1.64944e-05	0.00287175	utr-variant-3-prime, synonymous-codon, nc-transcript-variant	NEBL	GRCh38.p7	10:20785837	GCCATCGTCAATAGG[C/T]TGCACGTTGACGATG	10529
rs201578679	in-del	-/AAAAAAAAAAAAGAAAAGAAAAAAAAAT			intron-variant	NEBL	GRCh38.p7	10:21166234	CAAAAAAAAAAAAAA[-/AAAAAAAAAAAAGAAAAGAAAAAAAAAT]TTTCTACATCATGAT	10529
rs201579582	snp	C/G	0.00199806	0.0315443	intron-variant, downstream-variant-500B	NEBL	GRCh38.p7	10:20817589	GAAAAAAGTTACTAA[C/G]ATGATCACACATTGC	10529
rs201590910	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20888214	GTATTTTGCCTGGGG[A/G]AAAAAAAAACAGGAA	10529
rs201591974	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21078768	TATACTTGATCTTAT[C/T]TTTAGAAAGAAAAAG	10529
rs201596190	snp	A/G			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20870199	GGGCATGGTGTGTGC[A/G]CCTGTAATCCCAGCT	10529
rs201596786	snp	A/G	0.000790988	0.0198713	intron-variant	NEBL	GRCh38.p7	10:20828680	AAACTATGTGTGTGC[A/G]CACATGTGAGAGGGA	10529
rs201628197	in-del	-/AAAT	0.0980852	0.198549	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20868846	AGCCAAAAAAAAAAA[-/AAAT]AACAGACCTTCATCT	10529
rs201669624	in-del	-/G	0.0130921	0.0798413	intron-variant	NEBL	GRCh38.p7	10:20974292	GGGTCTCACTCTGTT[-/G]GCCCAGACTGGAATG	10529
rs201679619	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21000757	AATGGAGCAGATGAC[A/G]TCAGGTAAGATGTCT	10529
rs201682188	in-del	-/A			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20882751	CCAAAAAAAAAAAAA[-/A]TGTCATCTGGTATAA	10529
rs201700566	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:21026333	ACAGTACACTGTACA[C/G]CCCCTCCCTGACAGA	10529
rs201700991	in-del	-/CATT	0.00874735	0.0655527	intron-variant	NEBL	GRCh38.p7	10:20906878	CCTATTTCAATCATA[-/CATT]CATTTATGAAATATC	10529
rs201711832	in-del	-/A/AA	1.85012e-05	0.00304143	intron-variant, upstream-variant-2KB	NEBL, NEBL-AS1	GRCh38.p7	10:21172495	GAAAAAAAAAAAAAA[-/A/AA]CATTTAAAAATACAG	10529
rs201719568	snp	C/G	1.68269e-05	0.00290055	missense, intron-variant	C10orf113, NEBL	GRCh38.p7	10:21126110	TCTCGGCTCTCCGTT[C/G]TGCCTTACCAGGCCT	10529
rs201724074	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21046371	TAGGAAAATAGATTT[G/T]GTAGTGTTATACGAG	10529
rs201725204	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20814609	TCTCAAACACACACA[C/T]ACACACATACACACA	10529
rs201749466	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21093166	TTTTTTTTTTTTTTT[C/T]CATTTTAGCAGAGCC	10529
rs201760262	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:20968357	AAAAAAAAAAAAAAT[A/T]AAAATCAGCCAGGCA	10529
rs201763188	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:21004719	TCTCAAAAAAAAAAA[-/A]GAATCACCTGGAGAA	10529
rs201784969	in-del	-/TATTTTC			intron-variant	NEBL	GRCh38.p7	10:20801220	TTTATTTTTATTTTT[-/TATTTTC]TTTTGAGGCAGGGTC	10529
rs201787734	snp	G/T	0.00119737	0.0244387	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20858160	CTTCTAAGGAAGCAG[G/T]TGAGCACATGAACGC	10529
rs201799790	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20909150	CGTTTGAGTTACAAA[A/C]ATCCAACTACACTCT	10529
rs201803330	snp	G/T			intron-variant, missense, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20859772	CACTTTCAAGAGGAT[G/T]GTAATGATGTTTCTT	10529
rs201813414	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:20973239	TAAAAAAGATATTTT[A/T]CCTTTTTCTTTTTTT	10529
rs201817693	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20989305	AGGTTTTTTGTTTTT[A/C]TTTTTGGAGGAAATG	10529
rs201822024	snp	C/T	0.000960153	0.0218896	intron-variant, nc-transcript-variant	NEBL	GRCh38.p7	10:20813933	AATGATCTGGTTGGA[C/T]CCTACCATTGAAATA	10529
rs201830841	snp	A/G	1.64822e-05	0.00287068	intron-variant	NEBL	GRCh38.p7	10:20897084	CTCATTGTCAATTTA[A/G]AGGAACAAACGCTGG	10529
rs201832837	snp	C/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20809656	CATAAATGACTAATT[C/G]TATTTAAAAGTAGCA	10529
rs201838351	snp	C/T	0.000220836	0.0105057	missense, utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20787222	TTGGTGAATGCTGCA[C/T]TGATCTCATGGATGA	10529
rs201858785	snp	A/T	0.000399281	0.0141238	intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20808518	TTGATACCTCCTTCA[A/T]CAGACGGTCTTGTTA	10529
rs201869237	snp	C/G	0.000412014	0.014347	intron-variant	NEBL	GRCh38.p7	10:21020207	CGGGTAGTGTCTGTG[C/G]GGAAATTTTTTAAAA	10529
rs201878523	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20914038	TCAGGTTCAACCTCC[C/T]CTGCACAGACTATGA	10529
rs201889441	snp	C/T	0.000399281	0.0141238	missense, upstream-variant-2KB	NEBL	GRCh38.p7	10:20961769	TCTTCAAAATCTCTT[C/T]TGTACTTGACCTAAC	10529
rs201892761	in-del	-/TA	0.029116	0.117091	intron-variant	NEBL	GRCh38.p7	10:20789910	ATGTATAGATATATG[-/TA]TATATATATGTGTGT	10529
rs201899392	snp	C/G	0.000152229	0.00872303	intron-variant	NEBL	GRCh38.p7	10:20889818	AAAGATAAATGCAAG[C/G]CAGTTTGCAAGCTTT	10529
rs201919304	in-del	-/A	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:21007985	AATAAGGTGACTGTT[-/A]AGAGTGTCCAGCAGT	10529
rs201919969	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21029993	GACGTCCCCCGTCCC[A/G]CTCAAAGACCCAAAC	10529
rs201938639	in-del	-/G			intron-variant	NEBL	GRCh38.p7	10:20994885	GGAGGAGGAGGTAGA[-/G]GGGGGGGTTGGTCTT	10529
rs201945904	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:20792818	CAAAAAAAAAAAAAA[G/T]AAAACTCCTGTCTAG	10529
rs201962574	in-del	-/TTAT			intron-variant	NEBL	GRCh38.p7	10:21034944	ACTAGCTATTTATTC[-/TTAT]TTATTTATTTATTTA	10529
rs201963477	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21097228	GAGGTCCGGGGGGGG[A/G]GTGGGGCAGATCACA	10529
rs201974015	in-del	-/T			intron-variant	NEBL	GRCh38.p7	10:20973248	TATTTTACCTTTTTC[-/T]TTTTTTTTTTTTTTA	10529
rs201982292	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21166251	AAAAAAAAAAGAAAA[A/G]AAAAAAAAATTTTCT	10529
rs201990747	snp	C/T	0.000399281	0.0141238	intron-variant, missense, nc-transcript-variant, upstream-variant-2KB	NEBL, LOC102725112	GRCh38.p7	10:20845289	GTGATGTACTTTACA[C/T]GTAAAAATTCTGGAG	10529
rs201993563	in-del	-/C			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20855536	AAAACAAAAAAAAAA[-/C]GAAGGAAAACTTAAT	10529
rs201996343	snp	A/G	0.00107781	0.0231893	missense, intron-variant, utr-variant-3-prime	C10orf113, NEBL	GRCh38.p7	10:21126067	CTTCTGGTCTCCCCA[A/G]CCAGCTTCCTGGGAG	10529
rs202003406	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21089845	AAAACAGATGGGTTT[C/T]CCAAAAACATGTCCA	10529
rs202025381	in-del	-/GA			intron-variant	NEBL	GRCh38.p7	10:21048591	AGAATCAATAAGAGG[-/GA]GAGAGAGAGAAATTC	10529
rs202038562	in-del	-/C	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20982723	TCTTAGTATGGCCTT[-/C]CCCCCCAAAAAATTT	10529
rs202048892	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:20837326	TAGAGAAAGTTTTAG[A/T]GGTCTGAATAGGTCA	10529
rs202049624	in-del	-/T			intron-variant	NEBL	GRCh38.p7	10:20931264	TCTTCTGCAATGAGA[-/T]TTTTTAAAAAAAAAT	10529
rs202056375	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20980390	AAAGAACCAGAAAAA[A/G]AAAAAAAAATATATT	10529
rs202056655	in-del	-/G			intron-variant	NEBL	GRCh38.p7	10:21086688	AAGCCAAGGTGGGTG[-/G]ATGAGTTAAGCCAGG	10529
rs202057004	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20797435	AGACATCCTAAGTGA[A/C]AAGCCACACTAAATA	10529
rs202059373	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21037443	GAACAAATTGCAAAG[C/T]AAAAAAATGGGAATC	10529
rs202060386	in-del	-/A	0.370162	0.219229	intron-variant	NEBL	GRCh38.p7	10:20976338	CTGAGACTCTATATT[-/A]AAAAAAAAAAAAAAA	10529
rs202083050	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21027341	GTTTTTTTTTTTTTA[A/T]TTTTCAGATAGAGTC	10529
rs202087654	snp	A/G	0.406986	0.194565	intron-variant	NEBL	GRCh38.p7	10:20896500	TATATATATATATAT[A/G]TATATATATATATAT	10529
rs202089400	snp	A/C			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21143858	CAGATCAGGATAAGA[A/C]AAGAAAAGAAAAAAA	10529
rs202106146	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21015662	GACTACAGGTATGCA[C/T]TATCATGCCCTAATT	10529
rs202112717	snp	C/G	0.000657268	0.0181163	NEBL	10	allele_origin=G(germline)/C(germline)	10:20840775	TCGCTTTGCTCTTTG[C/G]ATATCAAGAACTTCT	10529
rs202127185	snp	C/T	0.000676707	0.0183819	intron-variant, synonymous-codon, nc-transcript-variant	NEBL	GRCh38.p7	10:20808598	GTCGTCTCCGAGACC[C/T]GTACCGAAAGTACTG	10529
rs202130632	snp	A/G	4.94311e-05	0.00497123	intron-variant, synonymous-codon, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20880839	ATGTTTAACCTCAGG[A/G]GGCTCCTTCATGTGG	10529
rs202147389	snp	A/G	4.94597e-05	0.00497266	intron-variant, synonymous-codon, nc-transcript-variant	NEBL	GRCh38.p7	10:20817609	TCACACATTGCTGAT[A/G]TTTTTCTGGTTTTCT	10529
rs202147866	snp	A/G			upstream-variant-2KB, intron-variant	C10orf113, NEBL	GRCh38.p7	10:21146847	CTGGTCTATTATTTT[A/G]ATAATCAATTCGGAC	10529
rs202159958	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21070233	TGAGTCGTCAGGACC[C/T]CAGTTTTGTGTCTGC	10529
rs202161513	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21107492	TTTGCATATGTTGAA[C/T]CAGCCTTGCATCCCA	10529
rs202168481	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21037451	TGCAAAGAAAAAAAA[G/T]GGGAATCAGAAATAC	10529
rs202171786	snp	A/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21102287	ATATAATTGGCTCAC[A/T]ATATAATGCATATAT	10529
rs202184399	snp	A/G	0.000164897	0.00907861	stop-gained, synonymous-codon, utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20785903	CTGGGCACTGTAATC[A/G]TACATGGCTCGGTAG	10529
rs202189444	in-del	-/CCCA			intron-variant	NEBL	GRCh38.p7	10:21041348	TAGAGCTACAGATGT[-/CCCA]TCAAAAGCTTGCAAA	10529
rs202215550	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:20981405	TCTACTGCATCTCAT[-/A]AAAAAAAACACACAC	10529
rs202216448	snp	C/T	0.00199802	0.0315439	intron-variant, missense, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20859759	TGCCTAAAAGAAGCA[C/T]TTTCAAGAGGATTGT	10529
rs202223565	snp	A/G	0.0119091	0.0762411	intron-variant	NEBL	GRCh38.p7	10:20953666	AATCCTTTGATAAAA[A/G]TATAGAAGTCACTGA	10529
rs202225407	in-del	-/A	0.00676609	0.0577691	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21142500	CCTGTGAAACAAACT[-/A]AACAAGACAAAGAAG	10529
rs202237345	snp	A/C			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21135864	CTCTTCCTCCTCAAA[A/C]CCGGCCAGGATGAGA	10529
rs202239159	snp	C/T	1.65438e-05	0.00287605	intron-variant, downstream-variant-500B	NEBL	GRCh38.p7	10:20815591	ATAAAAGACACATCC[C/T]TTGTGATAGTCTAAA	10529
rs207470748	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20807801	AATGAGGTGAGGAAA[A/C]ATTTTAGTCTTAACC	10529
rs207470749	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:20890018	GCCTTTTTTGAATGA[A/T]AATTAGGTTGATAAA	10529
rs267602436	snp	C/T			utr-variant-3-prime, stop-gained, nc-transcript-variant	NEBL	GRCh38.p7	10:20785819	CACTGTGCCGTACAT[C/T]CAGCCATCGTCAATA	10529
rs267602437	snp	C/T			intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20808516	GTTTGATACCTCCTT[C/T]ATCAGACGGTCTTGT	10529
rs267602438	snp	C/T			intron-variant, synonymous-codon, nc-transcript-variant	NEBL	GRCh38.p7	10:20808565	AAAGCTAGGGTAAAT[C/T]TCGGAGATTTCTGAC	10529
rs267602439	snp	A/T			intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20835593	TTCCTTTCCCTTTAA[A/T]TATTGACTCCAGGTC	10529
rs267602440	snp	C/T			intron-variant, missense, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20850469	CAAGCATTGGCTTTC[C/T]CTTATTTTTCTCATA	10529
rs367548120	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21042592	TGCCATCAGGATGTG[C/T]CTTTGCACTGTTCTT	10529
rs367558902	snp	A/C			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20876208	TCCAAAAGAAGGAGT[A/C]AAATACAGAGTTATG	10529
rs367567398	snp	C/T	3.29506e-05	0.00405884	synonymous-codon	NEBL	GRCh38.p7	10:21020189	CGTGGTGAAGGACTG[C/T]TTCGGGTAGTGTCTG	10529
rs367569282	snp	A/G/T	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:21057282	TCTTTGACTTTTGGC[A/G/T]GTAAGGCAGAGTAAT	10529
rs367572658	snp	A/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20849356	TTTATTGAAAAAAAA[A/T]CAATCAAATACGCCG	10529
rs367574627	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20825836	AGAGGACCCCTCCCC[C/T]CAGTCTAAAGGTTAC	10529
rs367574641	snp	C/T	0.000153988	0.00877328	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20852523	GGCAGGGAGGGTAGG[C/T]ACCGTACGGGCAAGT	10529
rs367577430	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21055032	GGAGATGAACTTCTA[C/T]CCTGAAGAAGAAAAT	10529
rs367577847	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:21084345	TGTAACAGTTTTATG[C/G]GCAAGAGTCTATAGT	10529
rs367584888	snp	C/T	0.00914312	0.0669923	intron-variant	NEBL	GRCh38.p7	10:20992863	GCTCACTGCAAGCTC[C/T]GCCTCCCAGGTTCAT	10529
rs367586213	snp	C/G	1.6477e-05	0.00287024	intron-variant, missense, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20880841	GTTTAACCTCAGGGG[C/G]CTCCTTCATGTGGGC	10529
rs367588562	snp	C/G/T	1.65902e-05	0.00288008	intron-variant, splice-acceptor-variant	NEBL	GRCh38.p7	10:20815719	CCTCTGTAATAAACC[C/G/T]ATCATTTCAGAGAAC	10529
rs367617605	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20890987	GTTTCAGATGATAAA[C/T]TATATGTTCTCCCTA	10529
rs367620077	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21081530	AAGAAATTGATATTT[A/G]ACACACACATATAAA	10529
rs367623252	in-del	-/G/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20851989	CTGGAACTGACATCT[-/G/T]TTGCAACTATTTAAG	10529
rs367631839	in-del	-/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20851990	TGGAACTGACATYTT[-/T]TKCAACTATTTAAGC	10529
rs367632623	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20795080	AAGAAATGACAAAAC[A/G]GTGTGAGATTAATTT	10529
rs367637517	snp	C/G	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:20829767	ATGCAGGAAATCTGA[C/G]AGCTCAGGCACCTTC	10529
rs367638229	snp	A/C/T			intron-variant	NEBL	GRCh38.p7	10:20940026	TATTAGACAGATCAA[A/C/T]GAGACAGAAAGTTAA	10529
rs367643881	snp	A/G			upstream-variant-2KB	NEBL	GRCh38.p7	10:21175549	AAAAGAAAACCATTG[A/G]TTTCTGGGCCTCTTA	10529
rs367678869	snp	C/G			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21143737	ACGTGTTCAATAAGT[C/G]ACTTGAACCAGAGAG	10529
rs367684707	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21108707	GCTGGGTTCAAGTCC[G/T]GGATATCCTTGTTAA	10529
rs367688258	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21111540	ACTGGCTAGCCACGT[A/G]TAGAAAGCTGAAACT	10529
rs367705889	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21100279	AGCCGGTCCTTTTCC[A/G]CGCTGTGCTGTTGAC	10529
rs367719563	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:20919151	AAAAAATATTTTGTG[G/T]CAAGAGAAGGCATCT	10529
rs367767093	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20916484	CGATCTTGGCTCACC[A/G]CAACCTTCACCTCCC	10529
rs367771080	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21073731	TGTATTTCTAGGCAA[A/C]CTGTTAACATACATG	10529
rs367772718	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21122233	GTTTCACCATGTTGG[C/T]CAGGCTGGTCTCAAA	10529
rs367784222	snp	C/T			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21136921	GATTGGTAGAATTAA[C/T]GGACATCTAGAGACA	10529
rs367788442	in-del	-/G			intron-variant	NEBL	GRCh38.p7	10:20943997	TAATGAACAAGAGGC[-/G]GGTTAAGTTTTGGAG	10529
rs367798802	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:20950291	TCAAAAGTGGTATCA[G/T]CTAGAAATGTTTGTT	10529
rs367809780	snp	A/G			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21126192	AGGAAAAAAAATACC[A/G]CATTTGGAATAATAA	10529
rs367835722	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20873893	ATTCCTCCATTTCTT[C/T]GAATATTTTATTATA	10529
rs367844446	snp	C/G	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:20827634	TTAATTAATAGTGCT[C/G]ATGCACTATTTACAA	10529
rs367851566	snp	A/G			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20851734	AGGTTGCAGTGAACC[A/G]AGATCACGCCATTGC	10529
rs367852206	snp	C/G	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20820172	GTATAAAGAAACCTT[C/G]AACTTCAAAGGTTCT	10529
rs367852361	in-del	-/A/AA	0.0447077	0.143781	intron-variant	NEBL	GRCh38.p7	10:20896579	AGGCCCCAAAATGTT[-/A/AA]AAAAAAATGACTATT	10529
rs367853639	snp	G/T			intron-variant, upstream-variant-2KB	NEBL, LOC102725112	GRCh38.p7	10:20844114	TATAGAAATTACATG[G/T]CTATTTCAGCACATT	10529
rs367862225	snp	A/G			intron-variant, downstream-variant-500B	NEBL	GRCh38.p7	10:20813523	ACACTTTAAATGGGC[A/G]AACTTTATGGTAGGT	10529
rs367875839	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:20843406	CTACCCTGATGCATG[G/T]ATTCTGAATTAATAA	10529
rs367875951	snp	C/G			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20856641	AGGAATGTAAAAAGA[C/G]GTGTGGGAATGAAGA	10529
rs367901071	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20956417	ATGCTACTGACCCCA[C/T]TATTTACTGGGAATT	10529
rs367910740	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:20798933	TGACATTTCTTTCAT[G/T]CCATTTCTATTGAGA	10529
rs367918391	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20989476	AACGTAACTCCAACC[A/G]AAATTCCAAAAAATG	10529
rs367919279	snp	A/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20881857	AATATACTAAAAGCT[A/T]AATACTAAAAGGATG	10529
rs367927974	snp	C/G	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:20981501	TTGTCATTCCTTGAG[C/G]AGTCAGCAACCTACA	10529
rs367929319	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20827402	GACCCAGCAGACATC[C/T]GACCAGCTTACTCTG	10529
rs367932886	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21091526	CCAATTAGCTATCAG[G/T]ACCTCAAGTTTCCTC	10529
rs367933003	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21010887	TCTTCCAATGTGAAA[C/T]TGATTTGCCCATCAA	10529
rs367935230	in-del	-/A	0.0792508	0.182605	intron-variant	NEBL	GRCh38.p7	10:20979071	AAACAATATTAGATG[-/A]AAAAAAAAGCAAGCT	10529
rs367937711	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20810479	GTGTATCTTAGGGAA[C/T]GCATATCTTATTAGA	10529
rs367954491	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20827343	TCCTCATCCTTCCAT[A/C]AAGACTTTCCCATTT	10529
rs367957794	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21106208	TAGATCCCATTTGTC[A/T]ATTTTGGCTTTTGTT	10529
rs367972751	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21067087	ACGCCATTCCCCTGC[C/T]TCAGCCTCCCGAGTA	10529
rs367974728	snp	A/C/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21042001	TGCCATCTTGGTTTT[A/C/G]GTGGGTTTTGTCCGG	10529
rs367984353	snp	A/G	1.69069e-05	0.00290743	intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20840785	CTTTGGATATCAAGA[A/G]CTTCTGAATTAAGTT	10529
rs367986765	snp	C/T	0.000132059	0.00812478	missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20812889	CAGGATCGTCCACGA[C/T]GGGAGTAAAGCCTCT	10529
rs367990406	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20817897	GTACTGTTTAAATAT[A/G]TCTTCAATAAATGCT	10529
rs367994671	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20833204	ATCTACATTCCAAGA[A/G]GGCAAACCCTAATGC	10529
rs368009448	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21010636	AGCATTAGGAAGTAA[A/C]ACTAAAATAAGACAT	10529
rs368011083	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20976644	TCGAGCTAGAGGCCA[C/T]TATCCTAAGCAAATT	10529
rs368013979	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21056169	GGTAGAGAATATTTT[A/G]CCATCATGAAGCTAT	10529
rs368015322	in-del	-/A			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21139987	AAACCCTGTCTCAAC[-/A]AAAAAAAAAAAAAAA	10529
rs368023644	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20799975	AGAGAGAGCGCACGC[A/G]TGTGAGAGAGCGAGC	10529
rs368024997	snp	G/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20968440	TACCTCAGCCCAGAA[G/T]TTCAAGGCTGCAGTG	10529
rs368053385	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21019543	AAAACGCTGCCACTC[A/G]CAACCCTAGTCTTAA	10529
rs368054883	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20904245	CAATTGAGTACTGTC[C/T]ATGAGACAGACCCTT	10529
rs368058293	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:20839805	AAACCTAAGACTTTG[A/T]TTGGAACTATAAAAA	10529
rs368070234	snp	C/G/T			intron-variant	NEBL	GRCh38.p7	10:21041180	CAGCATAATACCTGA[C/G/T]AGTTTTTCAGTCCTC	10529
rs368077103	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21064321	TTATAATGTTTTAGG[A/T]TTTCACTGCAAAGCC	10529
rs368077159	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	NEBL	GRCh38.p7	10:20958875	GGATAAAATACAACC[A/G]TAAATTTCAAATTGA	10529
rs368077685	snp	C/T	0.000412055	0.0143477	intron-variant	NEBL	GRCh38.p7	10:21020066	TCAGAAGAGCAGCCT[C/T]GTGAAAAATCTTTAG	10529
rs368084487	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21057139	GATTTCTGGGTGCCT[A/G]TGTCCCAGATCTTAT	10529
rs368097422	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20835144	AGTTCTGCTCAGAAA[C/T]TTGGAAATACAGATA	10529
rs368105518	snp	C/T	1.6522e-05	0.00287414	intron-variant, splice-donor-variant	NEBL	GRCh38.p7	10:20888096	TTTAGAAAAACCCTA[C/T]CTCACTCTGGAGCTG	10529
rs368108159	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21101407	AGTGATGGGTAGAAA[C/T]TTCTGGTAGTAGTTT	10529
rs368137216	snp	A/T			downstream-variant-500B	NEBL	GRCh38.p7	10:20779582	TGAAGAAAAAAAAAA[A/T]TCCCCTTTTACCTAC	10529
rs368139537	snp	A/G	0.000153988	0.00877328	intron-variant	NEBL	GRCh38.p7	10:20831155	ACATGGCAACATGAC[A/G]TTGGAATACACGATT	10529
rs368142915	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21045744	GTGGAGAAAAGGAAA[A/C]CCTTGTACATTGTTG	10529
rs368152607	snp	C/G	4.95724e-05	0.00497833	missense, intron-variant, utr-variant-3-prime	C10orf113, NEBL	GRCh38.p7	10:21126039	CCTGGCAAGCGTTGG[C/G]CAGCTTTGCAGCCTT	10529
rs368168626	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21039200	CTCTGATGATAGTTT[A/C]TTTTGCTGTGCAGAA	10529
rs368201712	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21066629	TTTATTTTAAGCCTC[C/T]GAATTTGCTTTAAAA	10529
rs368235219	snp	C/T	3.5727e-05	0.00422637	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21126168	TCAAGCCTGGTACCC[C/T]CCATAGAAAGGAAAA	10529
rs368243134	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20954393	AAAAAAAGACACAGC[A/C]CATTTCTTCATAGAG	10529
rs368247886	snp	A/C			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20875037	AGTCACTGCACCCAG[A/C]CTCACATTTTTCTAC	10529
rs368253265	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20997393	GGGGGCAAGGTGGGG[A/C]AGGAAGTGGCCACAG	10529
rs368260076	in-del	-/A/AA/AAA			intron-variant	NEBL	GRCh38.p7	10:21154458	GTGAGACTCTGCTTC[-/A/AA/AAA]AAAAAAAAAAAAAAA	10529
rs368263548	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21045094	CATCCACATTCTCAT[A/G]GGCCTCCATAAATTG	10529
rs368268112	snp	C/T	0.000461232	0.015179	NEBL	10	allele_origin=T(germline)/C(germline)	10:20897033	CTTATAGAAGACCTA[C/T]TTGAAAAAAAAGAAA	10529
rs368274354	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:20906420	ACACTAATTTATGAG[C/G]CTTATTCCAATTATT	10529
rs368277520	snp	C/T	0.000437904	0.0147905	intron-variant, downstream-variant-500B	NEBL	GRCh38.p7	10:20817546	CAATCCCTTCATTCA[C/T]ACGTGGACAATGCAT	10529
rs368283236	snp	A/G			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21126907	TTGAACCCAGGGCGG[A/G]GAAGTTCTAGTGAGC	10529
rs368288014	snp	C/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21154375	GAGGCAGGAGAATCA[C/G]TTGAACCTGGGAGGT	10529
rs368298346	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21171367	AAAAAAAAAAAGAAA[A/G]AAAGGAAAAGAAAGA	10529
rs368301127	snp	C/G/T			intron-variant	NEBL	GRCh38.p7	10:20806655	AATGTCAAGGTCCCC[C/G/T]CACCAGCCTCTAAGC	10529
rs368319058	in-del	-/T			intron-variant	NEBL	GRCh38.p7	10:21002175	GAGGGTTTTTTTTTT[-/T]ATGGTGATGAAACAT	10529
rs368319806	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20925661	ACACATTTAGAAAGA[C/T]GTTTGTTAACTAAGT	10529
rs368328326	snp	C/T	0.00557542	0.0525036	intron-variant	NEBL	GRCh38.p7	10:21151030	GCAATTCCCTGACCT[C/T]TGAGCATCACTGAAA	10529
rs368338074	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21091940	CCCACCTTGTCACTT[G/T]CAGATAGTTTTTTCT	10529
rs368344185	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20794691	AGGTAACATAAGACT[C/T]TACTTCCCCAGGAAT	10529
rs368345024	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20929375	TATTAAGGGTTGTGC[C/T]ATTTCTCCACCTGCC	10529
rs368349986	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:20975771	TGCCCAACCTAGCAC[G/T]AGCAAAATGAGGAAT	10529
rs368352851	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20964538	TTAAACCAGCTCTCA[C/T]GTGAACTCATTGTTG	10529
rs368353419	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20894616	ATGTGTATACAGATA[C/T]AAATTAAGCCAGAAT	10529
rs368353856	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21113159	AGGAGATTTTGATGA[G/T]GAGGAAACTGAAGAA	10529
rs368380718	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21054801	ATGACTTGGCACTTA[C/T]TCGGAGGCATACAGT	10529
rs368399042	in-del	-/TC			intron-variant	NEBL	GRCh38.p7	10:20912880	CCATAGTATGCCAAT[-/TC]TTTTTTTTTTTTTTT	10529
rs368405954	in-del	-/GAG	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21089049	GATGGTGCAGTGACA[-/GAG]GAGACAGAAAAAGGG	10529
rs368411657	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20916875	AAGTCCTGCAGTGTA[C/T]TGACATGGGGAAAAA	10529
rs368457241	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21007847	ATCTCATTACCACAC[C/T]TCCAGAAGTAACACT	10529
rs368457929	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21025171	AAAAAAAAGGAGGAA[G/T]GGATGAATTGACACA	10529
rs368463931	snp	A/G	0.000206911	0.0101692	intron-variant, utr-variant-5-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20897252	ATTTACTCATGTGGC[A/G]TCCTTTTCCATACCA	10529
rs368470506	in-del	-/TA			intron-variant	NEBL	GRCh38.p7	10:21043801	TATATTTATTCAACA[-/TA]GATGCATCAGACTAT	10529
rs368474172	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:21163308	GTGGTGGCAGGAAAT[C/G]CATGAAGCTCAGGAG	10529
rs368478009	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21037277	GGGGGTGGAGGGGGT[A/G]GGGAGAGGGAGAGAG	10529
rs368478134	snp	C/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20965859	GCCTCAGGGCCCTGG[C/T]GTCCCCGAAAGACCC	10529
rs368479028	in-del	-/ACACACACAC			intron-variant	NEBL	GRCh38.p7	10:20814618	CACACATACACACAT[-/ACACACACAC]ACACACACACACAAC	10529
rs368484062	snp	A/T	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:20891951	ACCAAGATAACAGGA[A/T]ATGATCATTGAAAGG	10529
rs368484860	in-del	-/A			upstream-variant-2KB, intron-variant	C10orf113, NEBL	GRCh38.p7	10:21146944	ATTCTGCACAGAAAA[-/A]TCAATGGCTTCTTGA	10529
rs368486961	snp	A/G			intron-variant, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20848493	GGACCAATATCAACC[A/G]TGGCCAGTTAGCAAC	10529
rs368491819	snp	G/T	4.0914e-05	0.00452276	intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20897170	CTTTTCTTCTTCAGT[G/T]TCATCTTTTATATCC	10529
rs368494211	snp	C/T	1.65329e-05	0.0028751	intron-variant, downstream-variant-500B	NEBL	GRCh38.p7	10:20815608	TGTGATAGTCTAAAA[C/T]GAAGAAAACCACTTG	10529
rs368494929	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21038068	CTCTAAAGTTATGAT[A/G]TCACATCTTCTTATC	10529
rs368496283	snp	A/G			upstream-variant-2KB, intron-variant	C10orf113, NEBL	GRCh38.p7	10:21147298	AAACTAGGAACCTTC[A/G]CCCAGTTTCTCAGAA	10529
rs368498688	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21171290	CAGTGAGCCAAGATC[A/G]TGCCATTGCACTACA	10529
rs368513995	snp	A/C/G	4.98716e-05	0.00499333	intron-variant, missense, synonymous-codon, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20859716	ATTACAACTTACATT[A/C/G]CTCGCCAGTGTAGCA	10529
rs368520016	snp	C/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20848227	AATGAAAAGAATGTA[C/T]AAAATACTTTATATA	10529
rs368522011	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:20804187	GAAGTGGTACCAGGT[G/T]CTATGAAGGAAAAAA	10529
rs368533483	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:21119730	CACTCAGGAAATTGA[C/G]CATTGATACAATATC	10529
rs368533836	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20994720	TAGTATGCTCTATAT[C/T]ATATACTGTGTTCTT	10529
rs368536433	snp	A/G			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20853277	AATTGGATGAAGGCT[A/G]CTATTTGGACATATA	10529
rs368541073	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21100173	TTTCCCTAATTAACC[C/T]CTGCTGCTGTGATCA	10529
rs368549226	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21033903	GGGCACAGTGGCTCA[C/T]GCTGGTACTCCCAGC	10529
rs368555996	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20796367	CTCAGTCTAAAACAA[A/G]AAAAAAAAAAAAAAA	10529
rs368565177	snp	C/G	0.00914312	0.0669923	intron-variant	NEBL	GRCh38.p7	10:20793420	CTGAGGACAGAGGAA[C/G]AATCAGTTACTTGCA	10529
rs368607075	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21104991	ATAAACATATTGTTT[C/T]TCCTTTTTAGTCTGC	10529
rs368619904	snp	A/G	0.000153988	0.00877328	intron-variant	NEBL	GRCh38.p7	10:20828520	CTTAAAAGAAGTAAT[A/G]GCTACTCACCGCACT	10529
rs368619937	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21079587	TCCCAGTATAAACAT[A/C]GGGAGGCTCAACAAC	10529
rs368628022	snp	A/G	1.65811e-05	0.00287929	intron-variant	NEBL	GRCh38.p7	10:20809794	TGGGATGAACTAAAA[A/G]GTGAGTAATACCAGA	10529
rs368628865	in-del	-/TAAA			intron-variant	NEBL	GRCh38.p7	10:20918862	CTCAAAAAAATAAAT[-/TAAA]TAAATAAATAAATAA	10529
rs368629331	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21104420	TTCCAGCAACATTTT[A/G]TAGTTTCCAGTGTAG	10529
rs368640272	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21086731	GCAGTGAGCCATGAT[C/T]GTGCCACTGCACTCC	10529
rs368645671	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20972685	CCGGGAGGCAGAGGC[C/T]GCAGTGAGCCAAGAT	10529
rs368646724	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:20825673	TGTCTCAAAAAAAAA[-/A]AAGAAACTCAATGTA	10529
rs368662042	snp	A/C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21014282	GAGTGAGCCATCAGG[A/C/T]CTGGCCTATTTTTTA	10529
rs368662605	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21167116	GACTCGTCACGAGAT[A/G]CACCCAGCCCAGCCT	10529
rs368663357	snp	A/G/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20884605	AGATGCTACAAAGAC[A/G/T]ATCAGAATAATAACA	10529
rs368677619	in-del	-/A/AA/GG	0.0013285	0.0257416	intron-variant	NEBL	GRCh38.p7	10:20809949	AGGAATTTAAAAAAG[-/A/AA/GG]GAAAAAAAAAAAAAA	10529
rs368683700	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21044106	ACAGAATGTTAAAAA[G/T]CCACCATAGGCAGGG	10529
rs368689858	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20980972	TTCCTTTTTAATCAA[C/T]AGAGATGGGGCCTCA	10529
rs368700843	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20999962	GAATATAATCAAGAC[A/G]ACGCCAGTAAGTGAT	10529
rs368714187	snp	A/G	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20894742	ACACGGTGAAACCCC[A/G]TCTCTACTAAAAAAA	10529
rs368719532	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20923461	AGGTGGGTGGATCAC[A/G]AGGTCAGGAGATCAA	10529
rs368726113	snp	A/G			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20862187	AGTCAGGGACCATCT[A/G]TGCATTTCTAAGAAA	10529
rs368737349	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21001482	CTATGGCATTATCAC[A/T]GATACTCCAGGGAAA	10529
rs368737737	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20787913	TATTCAGCTGACTTA[C/T]CAAGACTAAATAAGT	10529
rs368738017	in-del	-/TTGT	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:21122003	GGGGATTTCTCCTGG[-/TTGT]TTGTTGTTGTTGTTG	10529
rs368747244	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20888648	AGAGGGGAGTGAGTG[C/T]TTTTTTGTTGTTTAT	10529
rs368753620	snp	C/T	1.64749e-05	0.00287005	intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20835563	GCATTTCAAGGGTGT[C/T]AGTGCCAGCTTGCAT	10529
rs368771320	snp	A/G	0.000153988	0.00877328	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21146307	TGTCTCAGCACACCC[A/G]TGCAGTATAAACCTG	10529
rs368778134	snp	C/T	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:21096913	TGTGGGGAGCTCAGA[C/T]GAAATAGCTGGGTCT	10529
rs368783451	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20957115	ACCCTTGCACTCAAC[C/T]GAACTTTGAATCAAA	10529
rs368790819	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20949594	AATAGTAAAAACATA[C/T]TTATGAATTTTTAAT	10529
rs368793318	snp	A/G/T	4.94279e-05	0.00497107	NEBL	10	allele_origin=G(germline)/T(germline)	10:20819417	AAAGGAAACAGAAAC[A/G/T]ACTTGCCGCACTCAG	10529
rs368795599	snp	A/C/G			intron-variant	NEBL	GRCh38.p7	10:21057642	GCAACCTCTGCCTCC[A/C/G]AGGCTCGAGCAATCC	10529
rs368813684	snp	C/T	0.000153988	0.00877328	intron-variant	NEBL	GRCh38.p7	10:21020232	TTAAAAGGACATAAT[C/T]AAAATATTGTGCTAC	10529
rs368833181	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21036241	CGAGGCAGGAGGATT[G/T]CTTGATCCCAGAGAC	10529
rs368833909	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21170416	AGTTACAGGAAGAAT[A/G]GTTCACTTTCCTTTA	10529
rs368844527	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21082981	TGGCCAGGCTGGTCT[C/T]GAACTCCTGACCTCA	10529
rs368851853	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:20838044	ATGTTTTCGAGCCTG[C/G]TACTCAACATCCATT	10529
rs368855990	snp	A/T	0.0138799	0.0821421	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20846430	GAGAATAAGAGAAGC[A/T]TGCTGTCTCCTCACT	10529
rs368856187	snp	C/G/T	3.32896e-05	0.0040797	intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20888207	TGCCTTTGTATTTTG[C/G/T]CTGGGGGAAAAAAAA	10529
rs368860618	snp	A/T	0.00517822	0.0506191	intron-variant	NEBL	GRCh38.p7	10:21115572	TAAAGGTGCTGCTCC[A/T]TTGTCTTCCGACTTG	10529
rs368865696	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21024046	GCATCAAAGTTCTAT[G/T]TGGAAAAAGTGTTAC	10529
rs368867711	snp	A/T	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:21019844	TTAGGACCAAATAAG[A/T]CAAGATTGTTGGGAA	10529
rs368873365	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20833591	TGACTGGAAACCATT[A/G]AAGAATTGCATGTGA	10529
rs368888488	snp	C/T			intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20899215	TTACATTATCTTTAT[C/T]TGGAAATAGGGAGGA	10529
rs368896271	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20891433	AAAAAGTATCTCCGT[C/T]ATATAATTAAGTGTG	10529
rs368897595	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20905516	CACTCACTGTCACAA[C/T]AGCAGCATGTGGGAA	10529
rs368905591	snp	A/G	0.00597247	0.0543191	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20882317	GAAAGGAGAAAAGAA[A/G]GAAGAGGGGAGAGGA	10529
rs368927859	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21087942	TGCCCTGAATCTGAC[A/G]ATTTGCAATACCGAA	10529
rs368928524	in-del	-/A			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20865215	GAATTCATCTAAAAA[-/A]TGTAGAACAGAAAAC	10529
rs368929846	snp	A/C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20904742	TGAAAAGCATAAAAG[A/C/G]CTTCAGTAAATGCAA	10529
rs368938105	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21171008	CTTTGCTGCCTCCAG[A/G]CTATGCCAACCACAC	10529
rs368949395	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21117299	CAATTCTTGATTCTC[A/T]CCTGCATCTTTCTCT	10529
rs368952687	snp	A/G	0.0197687	0.0974348	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20959328	CCAGCATCTCTAGCC[A/G]GAAGATTCTGGGGTC	10529
rs368953696	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20993253	GGTCATGAAAGTTTT[A/G]CTAGCAAAGGACATT	10529
rs368960899	snp	C/T	0.00676609	0.0577691	intron-variant	NEBL	GRCh38.p7	10:21160707	TTAAAGTTCTGGAAA[C/T]GTGGGAGAAAAGGCA	10529
rs368965927	snp	C/T	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:21082950	GAATTTTTTTAGAGA[C/T]GGGGTTTCACCCTGT	10529
rs368975986	snp	A/G/T	1.64749e-05	0.00287005	intron-variant, synonymous-codon, nc-transcript-variant	NEBL	GRCh38.p7	10:20835558	ATGCTGCATTTCAAG[A/G/T]GTGTCAGTGCCAGCT	10529
rs368988054	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20820902	TACTCTTAGTAGTGA[A/G]CATGAGAGTGAAGGG	10529
rs368994470	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21042626	AACTTCAGATCATGT[A/G]ATGCCAGCTTGATGG	10529
rs368999635	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21066403	GTTGTTGATAAAATG[C/T]TTTTCATGCTAATGA	10529
rs369009994	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21053409	CAAGAGTCTGAAAGG[A/C]AACAGGCAAGAATAT	10529
rs369011895	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21081340	CTTTCATGGGAAGCA[A/G]GGGAAAGGCAGTCAG	10529
rs369037243	snp	A/G/T	0.000165505	0.00909551	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20852531	GGGTAGGTACCGTAC[A/G/T]GGCAAGTGTGTACCT	10529
rs369040992	snp	A/G	0.0322114	0.122752	utr-variant-5-prime, upstream-variant-2KB	NEBL, NEBL-AS1	GRCh38.p7	10:21173949	GGGCTGCGGGCGGCG[A/G]GCGCCGGGTAGGGAG	10529
rs369054210	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21047421	ACATGTGGGGTTCTG[A/C]AATGCTTTAGTTATT	10529
rs369057065	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21099624	GGCCGTAACTGCATT[C/T]GATATGAAAGATTGT	10529
rs369067171	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20969544	GACTTTTTTTCTTTT[C/T]TTTTTTTTTTTTTTT	10529
rs369080646	snp	A/T	0.00031864	0.0126182	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20859857	AATAGTACATGTAAC[A/T]TTACATTTAAAAGTA	10529
rs369083889	in-del	-/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20874911	ACCACACCCAGATAG[-/T]TTTTTGTATTTTTAG	10529
rs369106583	snp	A/G	0.000798403	0.0199641	intron-variant, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20873566	GAGAAAAAGAAAATA[A/G]TAATAATGATAGTCT	10529
rs369125916	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21017549	CTTGCAGCTGGCCAC[A/G]TCAGGGAGAATAAAA	10529
rs369127710	in-del	-/GACA			intron-variant	NEBL	GRCh38.p7	10:21117827	CAGGCTCTAGAGTCA[-/GACA]AACTGGGTTCAAGTA	10529
rs369128417	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20791620	ACCTAGTCTCAAATT[C/T]CCAGTCTCAAGCAAT	10529
rs369128594	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20988092	CTCTCCCCTTCTGCT[A/G]TCTGTGGGACTCTCC	10529
rs369133494	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20953302	CCCTCTCTCTCTCCA[C/T]ATGCACACACCAACG	10529
rs369133964	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21078067	GGTTGTGTGCAGAAT[A/G]GACGGGAGGAGGAGA	10529
rs369143293	in-del	-/T	0	0	intron-variant	NEBL	GRCh38.p7	10:21071813	TAGTGTTGGGCTTTT[-/T]GTTTTTGATTTTGTC	10529
rs369155112	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21037822	CTAATGAAGAGTAGA[A/T]AGATAGACAAAATGA	10529
rs369156794	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21169424	CCGGAGAAATTATGG[C/T]GGCCCTCTGGCCACA	10529
rs369160787	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20799954	GTGTGTGTGTGAGAC[A/G]GAGAAAGAGAGAGCG	10529
rs369168091	snp	G/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21089051	TGGTGCAGTGACAGA[G/T]GAGACAGAAAAAGGG	10529
rs369182388	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20794159	AGTGCCACGAGGCGA[A/G]GGGAAGCGGACCCCA	10529
rs369184227	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20823140	ATTTGACCTGTACAG[A/G]TTTTATGCTGTCATT	10529
rs369185283	snp	A/G	0.0205511	0.0992634	intron-variant	NEBL	GRCh38.p7	10:20950348	CACATTTGAAACTAC[A/G]ATAACTACTCCTTCA	10529
rs369192906	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20900776	CTTGAACTTGGGAGG[C/T]GTAGGTTGCAGTGAG	10529
rs369202483	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21009868	AATTTCTGCTTAAAA[C/T]ATATAATTTTTAAGC	10529
rs369211623	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21162064	ACAATCACATCACCA[A/G]TGAGTCAATCAATCA	10529
rs369219555	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:21013253	CATTCACCCATTCCT[C/G]TATGTGAAACGTAAT	10529
rs369221899	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20941708	TCAGCCCAAAACCTC[C/T]TTAATTAAGCTAATA	10529
rs369228991	snp	A/G	0.00716266	0.059414	intron-variant	NEBL	GRCh38.p7	10:21103308	AAGCTCCGCCTTCCG[A/G]GTTCATGCCATTCTC	10529
rs369249131	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20983502	AAAAACCTCTCTTTC[C/T]GTAAGTATTCCAATT	10529
rs369251360	snp	A/C			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20851619	TCTTTACTAAAAATA[A/C]AAAAAAAAAAAAAAA	10529
rs369252519	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20936837	CATCTCCCACCTTAT[A/G]AATAAGCTTGGGTCG	10529
rs369257417	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20993930	TTAGCCACCCATCGT[C/T]ATCTCACCCAAGGGC	10529
rs369258889	snp	A/G	0.00199481	0.0315187	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20851700	TGAGGCAGGAGAATC[A/G]CTTGAACCCAGGAGG	10529
rs369264298	in-del	-/T			intron-variant	NEBL	GRCh38.p7	10:21050289	GGCAACTTTTTTTTT[-/T]ACCTTTTCTCAATTC	10529
rs369265321	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20996831	AAAGCAGTTCCAACT[C/G]TCAATACTAACTGTT	10529
rs369274241	snp	C/T	1.67767e-05	0.00289622	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20868804	GTTAAATATTTCTAC[C/T]CTCCAATGATGAACT	10529
rs369276555	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20832037	AACTCAATGTTCCCA[C/T]TCCTAAACCATCCAG	10529
rs369287849	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20806788	TAAATGAATGAATGA[C/T]GGACTGAGGAGGATA	10529
rs369291648	snp	G/T	0.000137903	0.00830254	intron-variant, synonymous-codon, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20852632	TTTGTTTTCCTCAAA[G/T]AGCTTTTTATATTCT	10529
rs369292695	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21072289	CTCTTTTCCAGTTCC[A/G]TCTTTTATAATGTCA	10529
rs369297283	snp	A/G	3.32734e-05	0.00407868	intron-variant	NEBL	GRCh38.p7	10:20815728	TAAACCTATCATTTC[A/G]GAGAACAAAAAATAG	10529
rs369302001	snp	A/G	0.000153988	0.00877328	intron-variant	NEBL	GRCh38.p7	10:21020227	ATTTTTTAAAAGGAC[A/G]TAATTAAAATATTGT	10529
rs369320902	snp	A/C			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20845770	CAAACCACCTTCAAA[A/C]CCAAGCAGCATTAAT	10529
rs369323185	snp	G/T	0.00795532	0.062565	intron-variant	NEBL	GRCh38.p7	10:21114919	TATTAAAATGATTGA[G/T]TTTAAATATATCGTC	10529
rs369330878	snp	A/G			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20860418	CAATACTCTCTCTAA[A/G]TTGTTTGTCTCCTTT	10529
rs369339302	snp	A/T	0.00597247	0.0543191	intron-variant	NEBL	GRCh38.p7	10:21001665	AGCCCATTTATGCCT[A/T]GTGTTCCATCATTGG	10529
rs369343009	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:20841572	TGGAATCATCCATAG[A/T]TAATGAAATGTGCAT	10529
rs369343968	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20976631	GCAGCCACATGGATC[A/G]AGCTAGAGGCCATTA	10529
rs369351624	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20967385	GTGATCCCAGCACTT[C/T]GGGAGGCCGGGGCAG	10529
rs369360938	snp	A/T			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21139039	GTAATTTAGCCTTCA[A/T]ATCTGTTTGAAAGCA	10529
rs369363729	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20987850	TCAACAATCCTCTGA[C/T]ATCACTAGGACTTCC	10529
rs369364145	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:21162545	TCTCAATTCCTTACA[C/G]ACTTGCTCTTTAAAA	10529
rs369389414	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21171877	AGGAATACCCATGTC[C/T]TTGGTTCCATTCTCC	10529
rs369389846	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21004107	TTAAAGACATTTGAA[C/T]TTGAGCATCAGATTG	10529
rs369391342	in-del	-/T			intron-variant	NEBL	GRCh38.p7	10:20799519	AGATAGCACTTTTTT[-/T]GGACAAATGTAAACA	10529
rs369401462	snp	A/C/G	0.00011538	0.0075946	intron-variant	NEBL	GRCh38.p7	10:20819545	TGCAAGACAGTTTGA[A/C/G]ATTATGGGAAATAAA	10529
rs369405447	snp	G/T	1.6486e-05	0.00287102	missense, intron-variant	C10orf113, NEBL	GRCh38.p7	10:21146453	CAGCCAATATCTTCA[G/T]AAATTTCAGGTGCCA	10529
rs369419593	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20984743	CAACCCCCAGGCCAC[A/G]GACTGGTACCGGTCC	10529
rs369430626	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20974839	ACTTTTAAAAATTAA[C/T]GTGAATTTTCAACAG	10529
rs369447291	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21026007	CCTCTGTGTCTCACG[A/G]CCTTCATCTATATAG	10529
rs369447763	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21040400	ACTGCACAGGGTGCA[C/T]GGCACCAGCATCTGT	10529
rs369448880	in-del	-/T			intron-variant	NEBL	GRCh38.p7	10:21027326	CAACAACTTTTTTTG[-/T]TTTTTTTTTTTTTAA	10529
rs369457713	snp	A/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20870811	CCAAAGTATGGTAAG[A/T]AGAGATTTAAAGAGA	10529
rs369462358	snp	A/C			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21137322	ATAACAAATATCCAT[A/C]CAAACAACTGCGGTA	10529
rs369466710	snp	A/G	0.000153988	0.00877328	intron-variant, nc-transcript-variant	NEBL	GRCh38.p7	10:20813908	CGCCCATTCCTTAGC[A/G]TGTTTTAAGAATGAT	10529
rs369475722	in-del	-/TAAA			intron-variant	NEBL	GRCh38.p7	10:21046511	AAAATAATTAACAAA[-/TAAA]GGCAGACATATGACT	10529
rs369476525	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21063682	GCAGATCTCTTGAGT[A/T]GAGGAGTCTGAGACT	10529
rs369515771	snp	C/T	0.00557542	0.0525036	intron-variant	NEBL	GRCh38.p7	10:20967130	TCTCCAAAGAGAGAG[C/T]ATCTGGAGACCTGGA	10529
rs369519959	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21153887	TAAAAGTTAAGATGT[A/C]GGACCTCGTTATATT	10529
rs369533383	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21047076	TGATGAATGTTACTG[C/T]CATGCAGACTTTCCA	10529
rs369540413	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21088225	AAAACTTCTGTCCAG[G/T]CACAGTGGCTCACAC	10529
rs369551975	snp	A/G	0.0146672	0.084371	intron-variant	NEBL	GRCh38.p7	10:21055971	TTTGTTTGTCCTGAG[A/G]CTTTAGTTGTCTCTG	10529
rs369556718	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:21161202	TTATTTTTATTTTTT[C/G]TTATTTTTTATTAGA	10529
rs369562737	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21080149	GCACATAATTTATAA[A/T]GCATATAAAATATGG	10529
rs369570236	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21069591	CCTGAATCTCTTCAT[A/C]CTTCCACATTGAAGC	10529
rs369578766	snp	G/T			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21141403	TTCAGGAGAAAAAAA[G/T]AGCATATAGAGAAAA	10529
rs369605717	in-del	-/A			intron-variant, downstream-variant-500B	NEBL	GRCh38.p7	10:20817373	CCTGTCTCAAAAAAA[-/A]CAAAAAGAAAAAAGT	10529
rs369617058	snp	C/T			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21144926	AAAAAGTATTAAACA[C/T]GTTCAAGTATATAAA	10529
rs369617544	snp	A/G	0.00557542	0.0525036	intron-variant	NEBL	GRCh38.p7	10:21032444	CTGTAGTGTTGATGC[A/G]ATGTCTATTCATGAA	10529
rs369619534	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20839812	AGACTTTGATTGGAA[C/T]TATAAAAAGGGATGT	10529
rs369621860	snp	A/G/T	3.3122e-05	0.00406941	intron-variant, missense, nc-transcript-variant, upstream-variant-2KB	NEBL, LOC102725112	GRCh38.p7	10:20845290	TGATGTACTTTACAT[A/G/T]TAAAAATTCTGGAGT	10529
rs369627270	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21029124	AGTCAGCTGGGCTGA[G/T]GCAACAGATGACCTG	10529
rs369639481	snp	A/C			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20854750	CTTTATTTTTTGTGG[A/C]GCTAGGGTCCCACTA	10529
rs369653081	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21071146	ACTGCACTCCAGCCT[A/G]GGTGACAGTGACACT	10529
rs369656256	snp	C/T			upstream-variant-2KB, nc-transcript-variant	NEBL, NEBL-AS1	GRCh38.p7	10:21174751	TCTTCCGAGAGGACG[C/T]TTCTCCCTCGTGTCC	10529
rs369661575	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20810048	GACAAACTCACAGTG[C/T]TGCTGACTTCAGAAG	10529
rs369663870	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:20796234	AGGGCGTAGTGGTGG[C/G]CGCCCGTTATCCCAG	10529
rs369684450	snp	A/C			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21143448	AGTGAAACTTCATCT[A/C]AAAAAAAAAAAAAAA	10529
rs369708878	in-del	-/TCC			intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20960245	ATTTGCCAAAAATAA[-/TCC]AAAGAAAGAACTGTT	10529
rs369716928	snp	C/T	0.0111196	0.0737302	intron-variant, downstream-variant-500B	NEBL	GRCh38.p7	10:20817195	GACCAGCCCAAACCC[C/T]GTCTCTACAAAAAAT	10529
rs369745503	in-del	-/GATAT			intron-variant	NEBL	GRCh38.p7	10:21056991	GCTTTTTGCATATAT[-/GATAT]ATTTATCAAATAAAG	10529
rs369760300	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20934596	ACACCAGATACAGCT[C/T]ATCCAGTGGAGAATG	10529
rs369766203	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20833406	TGGCAAAGTCCCGAA[C/T]ATTGGTTGAAAATGA	10529
rs369777507	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20907470	TGAATAATAAACATT[C/T]GATAATTCTCTATCT	10529
rs369787029	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:21067988	TCAAAGAAAAAAAAA[-/A]TGTAATATACTTCCC	10529
rs369792617	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21117818	GTTATAAAACAGGCT[C/T]TAGAGTCAGACAAAC	10529
rs369796814	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21013603	AATAAGAGGGCCAGG[C/T]GCAGTGGCTCACGCC	10529
rs369801800	snp	A/G	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:20983561	ATCAAATTGCAAATC[A/G]TTGTACCCAAAATAT	10529
rs369808366	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21047882	AATCATGAAGAGATA[A/T]ATAAATTTCAAGTAT	10529
rs369842131	snp	A/C	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21012157	CCGATTTTCTGCTTG[A/C]TTCGTACAATCTACC	10529
rs369861167	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20907037	TTTAAGTGTTCAATG[A/G]TCAGATGTAGATAGT	10529
rs369862013	snp	C/T	0.000132009	0.00812324	intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20889862	CAGAAATAAAAGCAC[C/T]GATATTTTTTACATG	10529
rs369873436	snp	A/G	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:20791923	TCATTTAATTACTGC[A/G]ACAACTATCTAAAAC	10529
rs369876097	snp	C/T	0.00066968	0.0182864	intron-variant	NEBL	GRCh38.p7	10:20808685	GGGAAAATATTTACA[C/T]GTGTGATTAAGTGAC	10529
rs369884679	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:20902937	TAGAAAACAAATTAC[A/T]GAGTGTTCCCTTCAG	10529
rs369889514	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20885764	TTGTCACATATCAAG[C/T]GTTGGGTTGTAATTA	10529
rs369890935	snp	C/T	0.00119737	0.0244387	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20783104	TGTCAGCTTCATGCA[C/T]GAGATACCTGTTGCC	10529
rs369895384	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20971763	GGACTATAGGCGCCC[A/G]CCACCACACCCAGCT	10529
rs369906146	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21018244	ACTAATTTTAAATGA[C/T]TTTGCACAGTACCAA	10529
rs369912963	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20791800	TGTACCCACAAGAAA[C/T]GTTGAAGAGTACTCA	10529
rs369914980	snp	A/G			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20857126	CCATGCCCAGCCAGA[A/G]AAAAATAAACTTTTA	10529
rs369918547	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20793271	GACATGCCTAATCAT[A/C]GTGATACAAAATAAT	10529
rs369920142	in-del	-/GTTTACCTGA			intron-variant	NEBL	GRCh38.p7	10:20887227	CTGGATTCAAAATGA[-/GTTTACCTGA]TGACAATTCTTAAGT	10529
rs369925445	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21013457	TGCCAAAATGGCGTT[C/T]AAAGAAAAGAGAAAG	10529
rs369927283	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21063204	ATGCACACGCAGTTC[C/T]GATCTTGCTCCCCCA	10529
rs369937907	snp	A/G	2.01404e-05	0.00317329	intron-variant, upstream-variant-2KB	NEBL, NEBL-AS1	GRCh38.p7	10:21172509	AACATTTAAAAATAC[A/G]GTACAATGCCAGTTC	10529
rs369953758	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21113310	AAAAAAAAAAAACCA[A/G]GAAAAAACTCCTAAA	10529
rs369959760	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21034470	CTCAGCACAGTAACG[C/T]AGGCACCTGTTGCCA	10529
rs369970176	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20807114	TGGATCACTTGAGGT[C/G]AGGAGTTCCAGACCA	10529
rs369994500	snp	A/G	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:20798838	GCACATCGATGAAAG[A/G]CACATGTGCATTCTA	10529
rs370004442	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21074323	AGGCTTCAGGAGGCT[A/G]AAAGTTCATCACAGG	10529
rs370008434	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20801633	TTTATTTTTGTGTTC[C/T]CAGTATCTCACACAT	10529
rs370011417	snp	A/C/T	4.95809e-05	0.0049788	intron-variant	NEBL	GRCh38.p7	10:20785948	GAAGAAGGGATTATA[A/C/T]GATGAATGCCGAAAT	10529
rs370015531	snp	A/G	0.000297231	0.0121872	intron-variant	NEBL	GRCh38.p7	10:20826399	AAACATTTGTCTATA[A/G]TTTTGGTTTGCTTTT	10529
rs370026081	snp	C/G/T	0.000268753	0.0115892	intron-variant, upstream-variant-2KB	NEBL, LOC102725112	GRCh38.p7	10:20845253	AATAAACACCAAGAT[C/G/T]GTACCTCCCTCAGAA	10529
rs370051745	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20944243	CGTCTCTACTATAAG[C/T]ACAAAAATTAGCCAG	10529
rs370063661	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20792956	CTCAAGTCCTATTCA[C/T]ATCTGATCACAAGAC	10529
rs370067202	in-del	-/GT			intron-variant	NEBL	GRCh38.p7	10:21057303	CAGAGTAATGTGTGT[-/GT]AAGTAGTATTAATAG	10529
rs370081436	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:20934754	AAAATAAACCTCTAT[G/T]GTACTGAGATCTGAA	10529
rs370094745	snp	C/G	0.000247572	0.0111232	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20850378	TTAAACAATTAGTAA[C/G]AAACTAATTGACCTA	10529
rs370099281	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21052501	ACAAAGCCCACACAG[A/T]TCAAAGTCAGTGGAA	10529
rs370121895	snp	C/T			downstream-variant-500B	NEBL	GRCh38.p7	10:20779583	GAAGAAAAAAAAAAA[C/T]CCCCTTTTACCTACT	10529
rs370124609	in-del	-/AAG			intron-variant	NEBL	GRCh38.p7	10:21113100	AATAAGAATAAGAAG[-/AAG]GAGGAGGCGGAGGAA	10529
rs370130361	snp	C/T	0.0197687	0.0974348	intron-variant	NEBL	GRCh38.p7	10:21094277	GGAGGCCGAGGTGGG[C/T]GGATCACGAGGTCAG	10529
rs370131225	in-del	-/AT/TA	0.5	0	intron-variant	NEBL	GRCh38.p7	10:20929261	TGTGAGAGATATAAA[-/AT/TA]TATATATATATATAT	10529
rs370153729	snp	A/G	8.24545e-05	0.00642032	intron-variant, stop-gained, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20869787	TCTTGATGTCTGGTC[A/G]GTCAAGTTCTGCACT	10529
rs370164848	snp	A/G	0.000153988	0.00877328	intron-variant	NEBL	GRCh38.p7	10:20812975	CATACTGAATTTTGC[A/G]GATAGTTACCTCTTT	10529
rs370173091	snp	A/T			intron-variant, upstream-variant-2KB	NEBL, LOC102725112	GRCh38.p7	10:20843725	AATTGTACATATTTA[A/T]GGGATACAGAGTGAT	10529
rs370183738	in-del	-/GTTGTGTAAGCTGTGGATG			intron-variant	NEBL	GRCh38.p7	10:21120916	TGTAAGCTGTGGATG[-/GTTGTGTAAGCTGTGGATG]TTTACCATATTCTTT	10529
rs370201800	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21061347	TGTGATATGTAATAT[A/G]TTACATAATATATGG	10529
rs370206734	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20897288	CCCTTGAGATGCTGA[C/T]GTCTCTGGTGCTCTG	10529
rs370213341	snp	C/T	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20887535	GCAATCCTCCCACCT[C/T]AGCCTCCTGAGTAGC	10529
rs370214717	snp	C/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20871562	TTCTACTTACTCTTT[C/T]ATGAGCTTACATTTG	10529
rs370215867	snp	A/G			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21129788	AGAATCATATAAAAT[A/G]CACAATTAAAACCGT	10529
rs370237618	snp	C/T	0.000115566	0.00760063	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20868608	AATATTCTCCTGTGC[C/T]GTTAGAAACAAAATA	10529
rs370237640	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:21106049	TTTGTTTTTTTTCTG[C/G]TAAATTTGTTTAAGT	10529
rs370244060	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21097651	AGGTTTCCATGGCAA[A/G]CTACAAGAACAAATG	10529
rs370247545	in-del	-/A			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20870326	GTGGGACTTTATCTC[-/A]AAAAAAAAAAAAAAA	10529
rs370263195	in-del	-/T			intron-variant	NEBL	GRCh38.p7	10:20809274	AACTATTCATTTTTT[-/T]GCCTTTAATTATGAA	10529
rs370266379	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21002455	TTGTATTTTATTACA[A/G]AAATAAATTCTTAAA	10529
rs370271816	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20995962	ACCTCCATACTTCCA[A/C]TTTTAATCTTATAAA	10529
rs370281878	in-del	G/TT			intron-variant	NEBL	GRCh38.p7	10:20910834	TTCGTTTTTGTTTTT[G/TT]TTTTTTGGCCAAAGG	10529
rs370296547	in-del	-/GTTT			intron-variant	NEBL	GRCh38.p7	10:20910828	GTGTTTTTCGTTTTT[-/GTTT]TTTTTTTTTTGGCCA	10529
rs370310818	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21057637	TCACGGCAACCTCTG[C/T]CTCCGAGGCTCGAGC	10529
rs370330198	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:21067731	CCTATAATCCCAGCA[C/G]TTTGGGAGGCTGAGG	10529
rs370338380	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21097555	CAGCATGGCTTAAAT[G/T]AGTCATTTTGTATAT	10529
rs370346171	snp	A/G			intron-variant, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20884913	TTGTTAACAGGGGAT[A/G]GCTAATAAAATGGCC	10529
rs370351347	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21158355	AGCCAACATTTATAC[A/G]GTGTCTACTCTATGT	10529
rs370354925	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21095396	AGATGGCCAGGACCA[A/G]CTACAGATTCCCTTC	10529
rs370361923	snp	A/T	0.00159617	0.0282053	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20867254	TTTGAAAGAGTTAAC[A/T]TTTTTTAGGATGTTT	10529
rs370364851	snp	C/T	0.0150606	0.0854603	intron-variant	NEBL	GRCh38.p7	10:20932466	ATTAGGACAAACAAC[C/T]AATGTATGAAGGGCT	10529
rs370371741	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20906144	TCGTATTATGTAGAC[A/C]CTGAAATAAAATTTA	10529
rs370386622	snp	A/G	0.0162398	0.0886349	intron-variant	NEBL	GRCh38.p7	10:20939697	GGAAACCCATCTCAC[A/G]TGCAGAGACACACAT	10529
rs370405776	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:20980443	AGACACTGAAAGAAA[A/T]GTAGAGAAGAAAGAA	10529
rs370425241	snp	C/G	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20991771	CTCCCTCCCTCCCCC[C/G]CTCCCCTTTTTGGAA	10529
rs370431561	snp	A/T			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21140251	AGATTTGAATTGATT[A/T]TAGATGTGATTGAGT	10529
rs370434686	snp	A/G	0.00438332	0.0466095	intron-variant	NEBL	GRCh38.p7	10:21027565	GAACTCCTGGGCTCA[A/G]GTGGTCCAATCAATT	10529
rs370444208	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20986184	AGGTGCTTTTTCCAA[A/C]TTAGTACAATATAAC	10529
rs370445408	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21027327	CAACAACTTTTTTTG[G/T]TTTTTTTTTTTTAAT	10529
rs370451535	snp	G/T	0.000153988	0.00877328	missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20787272	TAGCCATAGCCTTGG[G/T]AATGGCTTTGCTGAT	10529
rs370456204	in-del	-/G			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20881170	TAGCTTAAACCTCGG[-/G]TGTAGTTTTGGGAAA	10529
rs370458891	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20956179	TTTGGAAACAAGAAA[A/G]GACCAAGAGGTAATT	10529
rs370466543	snp	A/T	0.0356815	0.128715	intron-variant	NEBL	GRCh38.p7	10:21010418	CCCAGCGAATTTTTT[A/T]ATTTTTTTTTTTTTT	10529
rs370475180	snp	C/T	1.6832e-05	0.00290099	intron-variant	NEBL	GRCh38.p7	10:20808697	ACACGTGTGATTAAG[C/T]GACTCGAAAAACAAA	10529
rs370507768	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20837075	GATTAGTAACCCTAC[A/G]ATGGCCCCTAGATGG	10529
rs370515471	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20894345	AGGCATGGTAGCACA[C/G]ACCTGTAGTCCTAGC	10529
rs370517546	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20807431	AACAACCAGTTTATA[A/G]TGATTTCATTAGTTA	10529
rs370538449	snp	A/G	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20950883	ACCAGGAAAGAGAGT[A/G]TGGATTTAGAAAAAA	10529
rs370541328	in-del	-/AAT	0.0123036	0.0774623	intron-variant	NEBL	GRCh38.p7	10:21071178	TGTCTCTAAACAATA[-/AAT]AATAATAATATTTTA	10529
rs370564342	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21002929	TACCCACAGTGTTCA[C/T]TCTAATTTAAAATGC	10529
rs370587416	snp	C/T	0.00636936	0.0560724	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20863938	TTGGAGGAGGGAGTG[C/T]TTGCCAGGATGGGAG	10529
rs370592420	snp	G/T	0.00438332	0.0466095	intron-variant, upstream-variant-2KB	NEBL, NEBL-AS1	GRCh38.p7	10:21173101	TCGCTCCTGGGTGTC[G/T]CTCTCCCGGGCTGTT	10529
rs370592765	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20822238	AGGGCATACCTCTCA[C/T]CTTTAAAATCCCCCA	10529
rs370612103	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20910554	TGAACCATGGTCAGA[A/G]AGACACTGTTTGAAA	10529
rs370613582	snp	A/G	0.00755907	0.0610114	intron-variant	NEBL	GRCh38.p7	10:20794686	GAAAGAGGTAACATA[A/G]GACTCTACTTCCCCA	10529
rs370629946	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21048652	GGGGCTGGCAAGTCC[A/C]AAATCTGCAGGGTAG	10529
rs370643849	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21161783	GGTAGCTTTGATGGC[A/G]ACAGTGTGAAGCATG	10529
rs370672129	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21116149	ATGCAGTATATTTAC[A/G]ATAGTTCTTTTAATG	10529
rs370697286	snp	C/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20862377	AACATAACTACATTA[C/T]ATAAAAAAATGCACG	10529
rs370699378	snp	A/G	0.000141713	0.00841645	intron-variant	NEBL	GRCh38.p7	10:20787357	CTTAAAGTTAGCCTC[A/G]AAATACCCATCCCAA	10529
rs370705101	snp	A/G	0.104149	0.203046	intron-variant	NEBL	GRCh38.p7	10:21028248	CTCAAAAAAAAAAAA[A/G]AAAAAAAAGAAGAAG	10529
rs370708490	snp	A/G	0.0023933	0.0345097	intron-variant, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20879821	GAAGTCAGGATGAGG[A/G]GATTTTAAAAAAAAG	10529
rs370709241	snp	A/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20988289	GTCCATGACTTTCCC[A/T]TTCCTCAGAAAAACC	10529
rs370719545	snp	G/T	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:21016492	AAGAAAGAGATAACA[G/T]TGGGTAACTATAAAT	10529
rs370737493	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20894589	AGAATTCTATTCGGA[A/C]GCAAAATGTGAATGT	10529
rs370741957	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20815925	AGGCACCTGCCACCA[C/T]GCCTGGCTAATTTTT	10529
rs370751232	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20947883	AATCTAACAAACACC[A/G]AATTATTTTCAGGTT	10529
rs370752023	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:21169759	TCAAGTAGACTTCCA[C/G]GTTCAAAATGAGGCA	10529
rs370752793	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20999156	AAACCCAGAGGTGTG[C/T]GGGGGGAAAAAAAAA	10529
rs370760345	snp	A/C			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21141372	GAGACATCTTATCTG[A/C]ACTTACCTCAATGGT	10529
rs370768909	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21067223	TGATCCGCCCACCTC[A/G]GCCTCCCAAAGTGCT	10529
rs370770885	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21040770	CCTCATTAGAGCTGA[C/T]TGGATCATGGGGGGA	10529
rs370775173	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20928784	TTTCTCCTACTCTAC[C/T]AGACCAATTCCATCA	10529
rs370779604	snp	A/G	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:21056556	TCACATCCTAGAAAT[A/G]TTGAACATGCATAGA	10529
rs370783594	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21041474	ACATGGAAAAAAGCC[A/G]AGAAGAAAAAGGAGA	10529
rs370789918	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20826280	CAAGGGGAACAAGGA[C/T]ACAGTTTTTGTTCTG	10529
rs370799176	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21101644	CTGTTGTTTGGCTTC[C/T]CTGTCACTTGCAGCC	10529
rs370807599	snp	C/G/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21091319	ATTTGAACTTGGATT[C/G/T]TCATTTTCCTCAAAA	10529
rs370810580	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20796274	AGGCTGAGGAGAATC[A/G]CTTGAACCCAGGAGG	10529
rs370812626	snp	A/C	0.000153988	0.00877328	intron-variant	NEBL	GRCh38.p7	10:20812734	GCATGATCTTTTCGA[A/C]CACACACACCGGCCG	10529
rs370814791	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20838362	GATGCAGTGGAAATA[A/G]CAAGAGAACTAGAAT	10529
rs370827941	snp	C/T	0.0197687	0.0974348	intron-variant	NEBL	GRCh38.p7	10:20941199	TCAATAAAATACTGG[C/T]AAACCAAATCCAGCA	10529
rs370831174	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21148621	ACTTCCACCTCCTGC[A/G]TGGAAGCGATTGGCC	10529
rs370838950	snp	A/G	0.000198537	0.00996139	intron-variant	NEBL	GRCh38.p7	10:20785959	TATACGATGAATGCC[A/G]AAATAGCTACAGCCA	10529
rs370842458	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:20929969	CAGGCTTGGTACTGG[C/G]CCACTTCTCATTTCT	10529
rs370854227	snp	A/C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20992696	CCTGAGCTACTTACT[A/C/G]TCCTCTACTAAAATT	10529
rs370856140	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21012928	AAAAGGATGCAGGTC[A/T]TCTCAGGAGGGTTGA	10529
rs370863784	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20887407	TGTGGATCCTGAATT[C/T]AACCTTTTTTTTTTT	10529
rs370877353	snp	A/C			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20873766	AATTTTAGTCAATTC[A/C]ACAAAACAAATAACT	10529
rs370883331	snp	C/T	0.00358779	0.0422022	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20849609	TCTCTGTCTTTCCAC[C/T]TTCTGCCATGGGATG	10529
rs370906784	snp	G/T			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21133153	TGTATGTGTGTGAGG[G/T]GGGAGTCCAATTTTA	10529
rs370921218	in-del	-/TC			intron-variant	NEBL	GRCh38.p7	10:20801174	TTCTCTACTTGGCTA[-/TC]TCTCTCTCTCTCTTT	10529
rs370924106	snp	C/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20946349	TGCTACTGGTAGTTA[C/G]CAGGATGAAGCTGAG	10529
rs370924189	snp	A/G	1.64787e-05	0.00287038	synonymous-codon, upstream-variant-2KB	NEBL	GRCh38.p7	10:20961729	AGGAGTGTCCGTGAC[A/G]ATGCTGAAGCCCCTC	10529
rs370928269	snp	A/G			intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20958333	GGGGGCAAGGAGAGG[A/G]TGGATGGCAATTAAG	10529
rs370948558	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21000081	TTGTAGTTTGGAAGG[C/T]GGCCCGTGGCAGTGT	10529
rs370953249	snp	G/T	0.000461893	0.0151899	intron-variant, missense, utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20815647	ATATTTTCTTGATTC[G/T]TCTTCACTCTTTCCA	10529
rs370957821	snp	A/G	0.000197968	0.00994709	intron-variant	NEBL	GRCh38.p7	10:20835643	AAAAGACAACATTTT[A/G]CAACATTCAAACACT	10529
rs370960171	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:20904668	TATGTACATTCACAC[A/T]TGCAACACACACACA	10529
rs370960795	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21028239	CTCAAACATCTCAAA[A/G]AAAAAAAAAAAAAAA	10529
rs370986434	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:21078549	TCTTCTTGAATCCCA[-/A]CACACACAGCCCCCA	10529
rs370990811	snp	A/C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20868412	AATGTGACAACATGG[A/C/T]TAGAGACATTGAAAA	10529
rs370991757	snp	C/G	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20834331	TATCTCTCAGGACGA[C/G]AACAGAAGTAGGAAA	10529
rs371001505	snp	A/G			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20850666	GTTAATGACATACAA[A/G]GAAAGTAAACAGGTA	10529
rs371021307	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20982127	AATTACCCACCCTAA[A/C]AGAAAAGTGGTTCAG	10529
rs371023901	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21154986	CGGGTGGATCACGAG[A/G]TCAGGAGTTCGAGAC	10529
rs371027415	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20971958	AACCAGAAGGTACCA[C/T]ACAAGGTTAAAATAA	10529
rs371033291	snp	C/T	1.64963e-05	0.00287192	missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20812858	ACCTGGGTGTTCTTC[C/T]TCACTCTCTCTGTCA	10529
rs371051911	snp	C/G/T	1.71888e-05	0.00293157	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20858359	CCTATGAAAATAACA[C/G/T]GGAACAAAATACCAT	10529
rs371057873	snp	A/G			intron-variant, utr-variant-5-prime, upstream-variant-2KB	NEBL	GRCh38.p7	10:20958981	GCTGAAAAAATTTCA[A/G]AACATTGACATAGAC	10529
rs371059596	snp	A/G			upstream-variant-2KB, intron-variant	NEBL, NEBL-AS1	GRCh38.p7	10:21175129	GATGTCAGGTTATTG[A/G]ACTCACTTGATGAGA	10529
rs371069212	snp	C/T	2.49199e-05	0.00352978	intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20897193	TTATATCCTCAAATA[C/T]AGGGACCCTCATTTT	10529
rs371074320	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21169075	AAAAAAAAATATATA[A/T]ATATATATATATATA	10529
rs371086755	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21166464	TAAACCTTTTAATAG[A/G]TGTGAGTGAGTTCTT	10529
rs371089211	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:20989262	TTACCTAGTTTAAAA[-/A]CATATTTAATCCAAC	10529
rs371098712	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21013282	ATCTCTTATCATTTA[C/T]GTTGCCTCAAAACCT	10529
rs371100252	snp	A/C/G	6.69931e-05	0.00578729	missense, upstream-variant-2KB	NEBL, NEBL-AS1	GRCh38.p7	10:21173803	CGGTGGGATACACGA[A/C/G]TTTTCCGCAACGGGC	10529
rs371102262	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21083450	GAACCAAAAGAGCCC[G/T]TCTGAGTTCTTTCTG	10529
rs371105861	snp	A/G	9.90818e-05	0.00703783	intron-variant, synonymous-codon, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20869824	GTGGGTGTCCTGCAC[A/G]TCTTTCCTATAAGAA	10529
rs371108601	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20953879	GCATTTATTGAGTAC[A/G]TGCTCTGTACTGAGC	10529
rs371113679	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20967559	CTTGAACCTGGGAGG[C/T]GGAGGTTGCAGTGAG	10529
rs371117432	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21166341	ATTCTCTTTTTAGTA[C/T]TTAAATGAATTCTGA	10529
rs371123700	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21165076	TTCCATTCACTATTA[A/T]AAGTAAAAGAGTGGA	10529
rs371130698	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21088337	AAGACCCTATTTCTG[A/C]GAAAACATTTTAATT	10529
rs371131996	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20838548	AGATTTAGGATACTA[C/T]AAAAACTTTGTCATT	10529
rs371151623	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21051983	TTGAAACCAGCCTGG[A/G]CAACACAGCAAGGCC	10529
rs371153307	snp	A/G	1.64827e-05	0.00287073	intron-variant, synonymous-codon, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20850431	CTCCTTTGAAGCTTG[A/G]TATGATGGTGTCTCA	10529
rs371169080	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20934954	GTGATTGGAAATGAA[A/T]CTGGAAATAAACTGG	10529
rs371178517	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21054537	CTGGCTCAAGAACAA[G/T]CTTTTTCTGTTTTCT	10529
rs371180696	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20984656	CATTCATTCTCTGTG[C/T]ACTTGGGCCCTGCAG	10529
rs371180860	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20978721	GATTGTGCCACTGCA[C/T]TCCAGCCTGGAAGCC	10529
rs371186480	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21162164	TGCACCAATGTGCCA[A/G]GAAGAAAACACATAT	10529
rs371202438	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20791388	TGAAAAGGGAGGAAG[A/G]AAAGTTTTGTTTTTT	10529
rs371205796	snp	C/G/T			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21130815	TTAATAATCTAACTT[C/G/T]CCACTTTAAGAAACT	10529
rs371221534	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21060817	TTGCTCAATCCAACC[A/G]TCAATCTTCAGTTCT	10529
rs371222835	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21014112	CAGTTGTAATTTTTC[A/C]TATTTTTTATTATTA	10529
rs371223337	snp	C/T			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21136421	GCAGTTTCAAACTTC[C/T]GGGTCCAAGCGATCC	10529
rs371225452	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20802064	TCCGGAGGAAAACAG[A/C]AACACATAGCATACC	10529
rs371227309	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:20897099	GAGGAACAAACGCTG[C/G]TCTGAGTATGTGTTT	10529
rs371243865	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20811406	AAATCAGAACCCCTG[A/C]ACTATCCCTTAAGAT	10529
rs371248634	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21039371	TGGGTTTTACGTTTA[A/T]GTCTTTAATCCATCT	10529
rs371266812	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21101730	TCTTCCAGACCCAAG[A/G]AGTGTCAAGCACGCC	10529
rs371271339	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20901340	GAGACACAGCCGTGG[A/C]CAAGGGAACGTATCT	10529
rs371280759	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21081310	GCTCCAGCAGCTGGC[A/G]CAGGATGACAAAGGC	10529
rs371283254	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20893065	CCTGGAAAATATTCT[C/T]CCTGCTGCCATGCAG	10529
rs371287073	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21078084	ACGGGAGGAGGAGAT[C/T]GGAAGATGGAAATGC	10529
rs371290087	snp	A/G			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20853914	CTAACAGAAAGAAAC[A/G]ACAAATGCTTGAACT	10529
rs371290840	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20833642	TTAATTGCCTCAAGG[A/T]TTCTTCTCCTGCTGG	10529
rs371321978	snp	G/T			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21134124	CCAGCTACTCAGGAG[G/T]CTGAGGCAGGAGAAT	10529
rs371327952	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21112120	GATGTGGAGAAATAG[A/G]AATGCTTTTACATGG	10529
rs371329351	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20972603	CAAAAAAAAATTAGC[C/T]GGGCATGGCAGTGCG	10529
rs371335098	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21103286	GGCTGCAATCTCGGC[C/T]CACTGCAAGCTCCGC	10529
rs371337259	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21045941	ATCACAGCACTATTC[A/G]CAATAGATAAGACAC	10529
rs371339328	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20955097	GAGAATAGCCCAAGT[A/C]AAGAGACTATTCCCA	10529
rs371363358	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:20973925	CATTTGAATCCTGAC[C/G]TCCCACTGTTCCTGA	10529
rs371386703	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21037692	ATTTTACTCTACATA[A/G]AATTTAAAAAGTGAT	10529
rs371399435	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21072745	GCTGTAATCCCAGTA[A/C]TTTGGGAGGCTGAGG	10529
rs371408984	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20786891	CATCAAATATCCATG[C/T]TCCTAAGGCATGAGT	10529
rs371410298	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21078861	TTATTAGCTGGCTGC[C/T]ACTTGGTGGCACTGT	10529
rs371412093	snp	C/G			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20876174	ATACTATTCAGAAGA[C/G]AGAAAAAGTTTTCAG	10529
rs371416318	snp	C/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20849111	CAGCATCCACTATTT[C/T]TATCCCTTTGCATTA	10529
rs371445303	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20950425	ACTCTAACAAGGAGA[C/T]GCCGGGTGTTCCTAA	10529
rs371454577	snp	A/G	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20914555	TCAATGCTTTCCTTG[A/G]TTATTGCTTTGTTCA	10529
rs371467724	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20956257	CTTTTCCCGAGGAGC[A/G]GTTGTTCAGAGGATC	10529
rs371471292	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20948044	TTTGTGCTGGGCCAC[A/G]TTCAAAGCTGTCCTG	10529
rs371471962	snp	G/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20965225	TTCATGGGGCTTATG[G/T]TAATTACAATGCAAG	10529
rs371485179	in-del	AAAA/T			intron-variant	NEBL	GRCh38.p7	10:21171342	TTCTGTCTCAAAAAA[AAAA/T]AAAAGAAAAAAAAAA	10529
rs371488895	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20906842	AACGAACAAAACCAA[A/C]AAAAATCTCTAACTT	10529
rs371494020	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20842006	TTTCTTACTTAATTG[C/T]GTATGAAAATCATAA	10529
rs371495012	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20827256	CCCGCGTGGGTGGGA[A/G]AGCACGGTAGGAGAG	10529
rs371502656	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20817875	TAGCAAGCACAAGTT[A/G]TTGCTGGTACTGTTT	10529
rs371520645	snp	C/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20884431	AAGCTTCTCCCTGCC[C/T]TCGCTTTCAGAAAAT	10529
rs371529649	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21076002	CTGCACACACATTAC[A/G]ATGGTCATGATTTTA	10529
rs371537488	snp	A/G/T	6.61653e-05	0.00575143	missense, stop-gained, intron-variant, utr-variant-3-prime	C10orf113, NEBL	GRCh38.p7	10:21126047	GCGTTGGCCAGCTTT[A/G/T]CAGCCTTCTGGTCTC	10529
rs371551337	snp	G/T	0.000115358	0.0075938	intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20817647	TCTTCAGCTCTGGTG[G/T]ATCAGAAATTGCAGT	10529
rs371553787	snp	A/G	1.65146e-05	0.0028735	intron-variant, stop-gained, nc-transcript-variant	NEBL	GRCh38.p7	10:20814019	GTCTACCTTTCATCT[A/G]TTTATGGTCCTGGGT	10529
rs371559533	snp	C/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20864766	AGTGAAAATAAGAAA[C/T]TAAACTTGCTGCCCA	10529
rs371568465	in-del	-/T	0.00676609	0.0577691	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21134839	ATTGTTCTCTTCCCC[-/T]GGAAGGTACGCTACT	10529
rs371596450	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20804071	GTTGCTGAATGCCTA[C/T]TCTAAGAGCTAGAGA	10529
rs371598499	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21044737	AAATGCCCCTGCTCC[A/G]TAAGCTCTTCTCCAT	10529
rs371613777	snp	C/T	0.0115144	0.0749975	intron-variant	NEBL	GRCh38.p7	10:20971594	AATGCTATCCCTCCC[C/T]CCTCCCCCAACCCTA	10529
rs371620771	snp	A/G/T	0.000115445	0.00759673	intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20888140	GCAAAAACACTGTCA[A/G/T]TTGTGGCTGGCATCC	10529
rs371630900	snp	C/T	0.000362854	0.0134646	intron-variant	NEBL	GRCh38.p7	10:20823201	AATACTTAAGAAATA[C/T]GATCACATTGCTGAT	10529
rs371638676	snp	A/G	0.000153988	0.00877328	synonymous-codon, intron-variant	C10orf113, NEBL	GRCh38.p7	10:21146470	AATTTCAGGTGCCAT[A/G]CTTTCCATAGAGTAG	10529
rs371643013	in-del	-/T	0.02016	0.0983543	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20868849	CAAAAAAAAAAAAAA[-/T]AACAGACCTTCATCT	10529
rs371645946	in-del	-/AT			intron-variant	NEBL	GRCh38.p7	10:20832455	GCCAGTGGGAAATGG[-/AT]TACCAATTGCTTACA	10529
rs371663324	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:20900846	TGAGACTCCATCCCG[-/A]AAAAAAAAAGAAAAA	10529
rs371683472	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21153406	GCTCACTGCAACCTC[C/T]GCCTCCCGGGTTCAA	10529
rs371711563	snp	C/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20862816	CCATATGACTGGCTT[C/T]ATTTACATTATGACT	10529
rs371714152	snp	A/G	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:20805671	CAGCCTGGCCAACAC[A/G]GTGAAACCCCATCTC	10529
rs371718265	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20940080	CAGCTCTGCACCAAG[C/T]GGACTTAATAGACAT	10529
rs371720999	in-del	-/GGAAAG			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20882367	AAGGGAAAGGGAAAG[-/GGAAAG]TAAAAGAAAAAGAAA	10529
rs371724530	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21025103	TGGAGTAAGAATGTA[A/G]GAAGAAGACACAGGG	10529
rs371725297	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20959518	AACCCAAGTTTCTTA[C/T]AGAAAAAGATCCTTG	10529
rs371738305	snp	C/T	1.65351e-05	0.00287528	intron-variant	NEBL	GRCh38.p7	10:20835674	CAGTGGGCAAACATG[C/T]ATCTGCAGTCAATGA	10529
rs371760760	in-del	-/AAA			intron-variant	NEBL	GRCh38.p7	10:20830912	CCATCTCTAAAATTT[-/AAA]AAAAAAAAAAAAAAA	10529
rs371780063	snp	C/T	1.65526e-05	0.00287681	intron-variant	NEBL	GRCh38.p7	10:20897117	TGAGTATGTGTTTTC[C/T]CACTCACCTGGTCTT	10529
rs371791358	snp	A/G			upstream-variant-2KB, intron-variant	C10orf113, NEBL	GRCh38.p7	10:21147729	TGTCCAGAACATTCT[A/G]TCTGGTTGCCCAGAG	10529
rs371793018	snp	A/G	0.00148248	0.0271853	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20852500	CCTCAGGATGGTTAC[A/G]GGTTGCTGGCAGGGA	10529
rs371794944	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:21057648	TCTGCCTCCGAGGCT[C/G]GAGCAATCCTCCCAC	10529
rs371798168	in-del	-/AT			intron-variant	NEBL	GRCh38.p7	10:20814616	CACACACATACACAC[-/AT]ACACACACACACACA	10529
rs371800445	in-del	-/TAGG			intron-variant	NEBL	GRCh38.p7	10:20797672	AGATTCCCTGCCAGG[-/TAGG]GAGGTCAACAGGTTG	10529
rs371805745	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20987151	TGTACTATCTGTACC[A/G]ACCGTTATGGGTAAA	10529
rs371806289	in-del	-/GGCATCTGTTGGCATCTGT			intron-variant	NEBL	GRCh38.p7	10:21011666	TCTGTTGGCATCTGT[-/GGCATCTGTTGGCATCTGT]TGGCATCTGTGGCTG	10529
rs371822147	snp	A/C	1.73375e-05	0.00294422	intron-variant	NEBL	GRCh38.p7	10:20812964	GGAAAAATCATCATA[A/C]TGAATTTTGCGGATA	10529
rs371825705	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21108628	TGGTGCTAAGAAGAA[G/T]GTATATTCAATTGAT	10529
rs371826961	snp	A/G	0.00318978	0.0398085	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20857191	CATTAAGGAAGGAAG[A/G]CAGTGGCAGTGATAT	10529
rs371830093	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20804511	AACTAACCAAGCACC[A/G]TTCCACTTAAGAGAG	10529
rs371836531	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21089688	TAGGTGAATGGGAAG[C/T]GGGGAGGCAGAGGCA	10529
rs371840761	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21051830	TACATATTCAATGTA[C/T]ACAACTCAATGATCA	10529
rs371850901	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21050991	GGCTTCCATCTATTA[C/T]GAACACTCCACTCAG	10529
rs371862080	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20931865	TTTCTATAGGTCAAA[C/T]TCAAGCCAAAGTAAG	10529
rs371864610	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20931991	CTAAGCTAACTGGCC[A/G]CACCACTCACCCATT	10529
rs371876327	in-del	-/AATAAAAA			intron-variant	NEBL	GRCh38.p7	10:21084613	AAAAAAAAATAAAAA[-/AATAAAAA]TAAAAAACAGCAACA	10529
rs371901801	in-del	-/A	0.288646	0.246995	intron-variant	NEBL	GRCh38.p7	10:21073322	GTGAGACCCTGTCTC[-/A]AAAAAAAAAAAAAGC	10529
rs371904337	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20799849	TTTGAAGTTTACAAC[A/G]TGATGGTATGGGATA	10529
rs371911969	snp	A/C	0.000164957	0.00908026	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20868632	CAAAATATCTGAATA[A/C]AGTCATTGTGGAATC	10529
rs371929683	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:20810739	CTGGAAAAGAAAAAC[C/G]TAGTTATAGACATAC	10529
rs371936568	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20803119	CCAAATATTAAAGGA[C/T]GTCTTTCTGGGACAT	10529
rs371942768	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21039726	ATAAAATGCAAGCTT[C/T]GGAATAATACCTAGA	10529
rs371952998	snp	A/G	0.000131865	0.00811882	intron-variant	NEBL	GRCh38.p7	10:21020080	TTGTGAAAAATCTTT[A/G]GGGCCAAGGGAACAA	10529
rs371967046	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20969631	ATTCACTGCAACCAC[C/T]GCCTCCCAGATTCAA	10529
rs371974416	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20888416	TAGAGAACGCTTTCA[A/G]TGAGACATGCAAGGA	10529
rs371975934	snp	A/G	0.000132122	0.00812672	intron-variant, synonymous-codon, utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20815676	CATTTCAGGAGTTAC[A/G]CTTAAAGTGGTAGCT	10529
rs371979535	in-del	-/TCTG			intron-variant	NEBL	GRCh38.p7	10:20921020	TGTCCACTGAAAATG[-/TCTG]GAGTAATGACAGTAG	10529
rs371984765	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20973589	TGTATCAGAAACCTA[C/T]AATTTGATCTACCCA	10529
rs371987727	in-del	-/AA			intron-variant	NEBL	GRCh38.p7	10:21010613	GCCATTMAAAAAAAA[-/AA]ATAAGAAAGCATTAG	10529
rs371988784	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20828294	TTTAAAATTTAGTTA[A/G]TAACTGTCATTTATA	10529
rs372003401	snp	A/C/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20888957	CTAGATTTCAGTATT[A/C/G]ATTTATTGAGCACAG	10529
rs372017708	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21095327	ATTCTAGCCTAAGAA[A/G]AGCAGATAAAAGATA	10529
rs372025171	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20839267	AACAACTTTTACACA[C/T]GCTACTGACAAGTAA	10529
rs372041776	snp	C/T	1.81063e-05	0.00300879	intron-variant, synonymous-codon, nc-transcript-variant	NEBL	GRCh38.p7	10:20828614	AGAAAGCATCTTCTC[C/T]GCTTCATCTTTATAC	10529
rs372053968	snp	A/C/T	5.06071e-05	0.00503005	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20880944	TCCCATTTAGAGGCA[A/C/T]ATAAATTCTTGCCTG	10529
rs372054285	snp	A/G	0.0378214	0.132213	intron-variant	NEBL	GRCh38.p7	10:20809949	AAGGAATTTAAAAAA[A/G]GAAAAAAAAAAAAAA	10529
rs372056784	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20820964	GGGGTAAGGTTCCTC[C/T]GGCCTCTTTCCTCGA	10529
rs372070640	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20834777	TCTTTACTCCAGTGA[C/T]CCTTTTATATTCTCA	10529
rs372077948	snp	C/T			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21145545	AAATGAATATGTATA[C/T]ACCTTTTCATAGCAC	10529
rs372085736	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:20791397	AGGAAGAAAAGTTTT[G/T]TTTTTTTGTTTGTTT	10529
rs372089312	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:21046000	TGAATGGATAAAAAA[-/A]TGTGGTACACACACA	10529
rs372108635	snp	C/G			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21136990	CTTTCTGGTGACTTC[C/G]CTGACTGGCATAGCA	10529
rs372120655	snp	A/C			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20856673	TGAAGTGCAAGCCAG[A/C]ATGATGTAAGTGTCC	10529
rs372131020	snp	A/G			intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20959779	AAGACATCGCAAAAA[A/G]TTTTTTTTTTAAAAA	10529
rs372177329	in-del	-/TTT			intron-variant	NEBL	GRCh38.p7	10:21066971	CTGAAATAATTTAAC[-/TTT]TTTTTTTTTTTTTTT	10529
rs372183052	snp	C/G			intron-variant, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20879820	AGAAGTCAGGATGAG[C/G]AGATTTTAAAAAAAA	10529
rs372196928	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21036100	CCCAGGGGGCAGAAG[A/G]TGCAGTGAGCCAAGA	10529
rs372202310	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20937897	AGGGTGGAGGAGGGG[C/T]GCCCGCCATTGCCCA	10529
rs372205956	snp	A/C/T	8.32832e-05	0.00645256	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20868788	GAATAAATAAGACAA[A/C/T]GTTAAATATTTCTAC	10529
rs372212312	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21059260	CATTCCACCAACCCA[A/G]GCACTCCGTATGGTC	10529
rs372215039	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20900548	CCGGGCATGGGCTGG[A/G]TGCGGTGGTTCACGC	10529
rs372223050	snp	C/T	0.00557542	0.0525036	intron-variant	NEBL	GRCh38.p7	10:20905505	TCATGAGAACTCACT[C/T]ACTGTCACAACAGCA	10529
rs372255097	snp	A/C/G	0.000798403	0.0199641	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21135011	CTCGATTATTCACCC[A/C/G]CTCCACCCTCCATCG	10529
rs372255579	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20925976	GCCATTCGTAAACAG[A/G]TGTCCATAACATATG	10529
rs372256814	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21160236	ACGTCTGCCAAACTG[C/T]CATTCTGCAGGACAC	10529
rs372258395	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20793225	AAAAATGAAGTGCTC[C/T]ATAATTGAGTTAAAA	10529
rs372264013	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21071575	TAAAAATATTAATCC[A/C]TTAACTCAGCCCTCA	10529
rs372268373	snp	C/T	6.6143e-05	0.0057504	intron-variant	NEBL	GRCh38.p7	10:20808480	TAAAAAATGAATCGA[C/T]TTTCTTTGTAAGCAG	10529
rs372281217	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20999095	TTTTATCTGCGGCAC[C/T]AAAAATTTCCAAATC	10529
rs372286090	in-del	-/CACACACACA			intron-variant	NEBL	GRCh38.p7	10:20814631	ATACACACACACACA[-/CACACACACA]ACTGGTTATCATATT	10529
rs372289439	snp	A/C	0.0154538	0.0865337	intron-variant	NEBL	GRCh38.p7	10:21031461	CCACGCCTATTCCTG[A/C]CGCGATGGGAGGCCC	10529
rs372289750	snp	A/G			upstream-variant-2KB	NEBL	GRCh38.p7	10:21176138	CTCCTGAGTACCTGC[A/G]ACCACAGGCATATGC	10529
rs372290689	snp	A/G	0.00755907	0.0610114	intron-variant	NEBL	GRCh38.p7	10:21101317	TCTCAGTTCTTCCAA[A/G]GTAAGACTTCATGCC	10529
rs372297961	snp	C/G	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:21089762	TTTCTCCCTCCTTCC[C/G]CTGCCCAGATAAACA	10529
rs372298386	snp	C/T			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21128583	AATCCACAGTAAGGA[C/T]CCTTAATTATTAAAG	10529
rs372306679	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20939405	ATTTTGTCACCACCA[A/G]GCCTGCCCTAAAAGA	10529
rs372306714	snp	C/T	1.65581e-05	0.00287728	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20852525	CAGGGAGGGTAGGTA[C/T]CGTACGGGCAAGTGT	10529
rs372316079	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:21034551	ATTTGACAATTTGCA[C/G]ATCAGTTATTTCCTA	10529
rs372327826	in-del	-/C			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21136730	CTCCATGTTCCAAAA[-/C]CCACCTCCACTTTCT	10529
rs372339940	in-del	-/GACT			intron-variant	NEBL	GRCh38.p7	10:20946974	CCCCAGAAACTGACT[-/GACT]CCAAAGAATTTGGTA	10529
rs372346639	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21084546	AGGTTGCAGTGAGCC[A/G]AGATCGTGCCACTGC	10529
rs372353616	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20834545	CAACAGTAACTTCCC[C/T]AGCAGCTAAGCAGCT	10529
rs372359596	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21047445	AGTTATTTCTATAGA[A/C]GAATCTATTAATAAT	10529
rs372364915	snp	C/T	5.09334e-05	0.00504619	intron-variant, missense, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20859790	AATGATGTTTCTTAT[C/T]CTTCATTTCATTATC	10529
rs372369741	snp	A/G	1.80481e-05	0.00300395	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20859673	AAAAAAACAAGAATC[A/G]AAAGATTTTGAAAAT	10529
rs372380661	snp	A/G			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20854534	GAAAGCACCCCCCAG[A/G]AAGGACATGAAAATG	10529
rs372383667	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21061178	TATATGTATTATATA[C/T]ATCATATGATGTATT	10529
rs372396804	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21075571	CAAATCCTTCCAGAA[A/G]CACGATGCAGTTGCC	10529
rs372397612	snp	A/G	0.00795532	0.062565	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21126520	AGAGATTTAGTCGTA[A/G]AATATTAGCATACAC	10529
rs372398420	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20886390	AAAAATTAGCTGGGT[A/G]TGGTGGTGTGCGCCT	10529
rs372443132	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21085307	TTTTTCCAATTGTGC[A/C]TTTTCAGTTAATTTG	10529
rs372449328	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21107899	GGTTTAGTCTTGGGA[A/G]GGTGTATGTGTCCAG	10529
rs372467659	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21032566	TCTGGTTGCAAACCA[A/T]CAATTTTATAATTTT	10529
rs372478855	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20791119	CAATGAAAATACACA[A/G]AAGTGTGACTCAACT	10529
rs372486387	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21121541	AATGTATGCCTATCA[C/T]GTGCACACTATATAA	10529
rs372492021	snp	A/C	0.000798403	0.0199641	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20860548	TAATTAGAATATAAA[A/C]ACAAGTTCACTACAA	10529
rs372499790	snp	C/G			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20875575	AGGCAACAGTGATTT[C/G]AGACTCTCTGGTAGG	10529
rs372506360	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21089504	AAAGAGGTGGGGGGT[A/G]ACACGGGTGAGTGTG	10529
rs372511658	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20967446	CAGCCTGGCCAACAT[A/G]GCCAAACCCTAGCTG	10529
rs372526855	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21057294	GGCGGTAAGGCAGAG[C/T]AATGTGTGTAAGTAG	10529
rs372532369	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:20995507	TCAGTGTAATTATGA[C/G]GGGATTTGCAGCAGC	10529
rs372559061	snp	A/G			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21134794	TTACTGAGTTCTGAC[A/G]AACATCAGTATTCAT	10529
rs372593687	snp	C/T	3.61363e-05	0.00425051	intron-variant, upstream-variant-2KB	NEBL, LOC102725112	GRCh38.p7	10:20845418	AAATATCAGTGACCA[C/T]TGAAAAGAGATTTGA	10529
rs372593752	snp	C/T	0.00557542	0.0525036	intron-variant	NEBL	GRCh38.p7	10:21075689	ATTGCAGTCATATCA[C/T]AGGATGCTTGATTTT	10529
rs372598136	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21082685	CAAGGATGGAAAAAG[A/T]ACTGTACTTATCACA	10529
rs372603264	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20834768	CCCAAAGCTTCTTTA[C/T]TCCAGTGATCCTTTT	10529
rs372629790	snp	A/G	3.30131e-05	0.00406269	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20868613	TCTCCTGTGCTGTTA[A/G]AAACAAAATATCTGA	10529
rs372638522	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21036299	TTTCTACAAAAAATT[A/C]TCAAATTAGCCAGGC	10529
rs372641477	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:21046277	ACAAAACTTCAGTTA[C/G]GATTAGTCAGTTCTG	10529
rs372642990	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21050144	AGAGCATACCATTCT[C/T]TATAATCTATCTTTG	10529
rs372650384	snp	C/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20872153	TTATATGGTGTTCAG[C/T]CTAATGACTGCGTGA	10529
rs372684856	snp	A/G	8.86627e-05	0.00665759	intron-variant	NEBL	GRCh38.p7	10:20823325	TTATAAGAATATAAC[A/G]TTAACTTTATTCTAT	10529
rs372694440	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20935191	TATAAAAGTCACCCC[A/G]AGGAAGCATCCACCA	10529
rs372700177	in-del	-/AT			intron-variant	NEBL	GRCh38.p7	10:20921795	ATGCACACACACACA[-/AT]TATGTATACACACAT	10529
rs372703156	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21002526	GTCCATTCTCACGCT[A/G]CTATAAAGAACTGAG	10529
rs372703562	snp	C/T	0.000423744	0.0145497	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21146310	CTCAGCACACCCATG[C/T]AGTATAAACCTGCCC	10529
rs372705921	in-del	-/G			intron-variant	NEBL	GRCh38.p7	10:20999526	TCACTTGAGCCCAGG[-/G]AGGTTGAGGCTGCAG	10529
rs372713294	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21113307	AAAAAAAAAAAAAAA[A/C]CAGGAAAAAACTCCT	10529
rs372717660	snp	A/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20943076	CCATTTGACCCAGCC[A/T]TCCCATTACTGGGTA	10529
rs372720124	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20902883	AGTTTTATGTGAGAT[G/T]TGTCAGGAATAATTG	10529
rs372726051	snp	C/T	1.89141e-05	0.00307518	intron-variant, missense, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20852648	AGCTTTTTATATTCT[C/T]GCTAAAATACAGAAT	10529
rs372726445	in-del	-/CT			intron-variant	NEBL	GRCh38.p7	10:21000638	GTTTAAATTGAAACT[-/CT]GAACATTTTGAGATA	10529
rs372730898	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20956795	AAGTTTGCTAAATAT[A/G]AAAAGAAAAAAATCT	10529
rs372731618	snp	C/T	3.33884e-05	0.00408572	intron-variant	NEBL	GRCh38.p7	10:20815741	TCAGAGAACAAAAAA[C/T]AGAATACTATGAATC	10529
rs372732985	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21063681	GGCAGATCTCTTGAG[C/T]TGAGGAGTCTGAGAC	10529
rs372742588	in-del	-/GTTT			intron-variant	NEBL	GRCh38.p7	10:21102825	GTTTTTTGTTTGTTT[-/GTTT]TATTTTTATTTTTAT	10529
rs372763596	snp	A/T	0.000153988	0.00877328	missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20812807	TCCATCTCCACGATG[A/T]GAGGGTGGACCCCTT	10529
rs372767246	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:20979515	TAATTCTCAGAAGAG[A/T]TCTAATATTATTACT	10529
rs372783278	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:20989832	CGTCTGCAGAGGTTG[C/G]GGGGTGGGCTGTGGA	10529
rs372788850	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20920866	CTAAGCTGAAATAAA[C/T]GGAACTAATTATACA	10529
rs372804145	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20928494	GAAACAAATCTTAAG[C/T]GCTAAGAAAAAGGAC	10529
rs372805426	snp	C/G	0.193966	0.243639	intron-variant	NEBL	GRCh38.p7	10:20941866	GAATAAAATACCTAG[C/G]AATCCAACTTACAAG	10529
rs372810152	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:20936750	TATAGTTTAATTTCT[G/T]CCTGTTCTAATTATT	10529
rs372817480	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20951536	TTTCTCTAATTGTAT[A/G]AACTTGGCTTAGATT	10529
rs372818596	snp	A/T			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21137971	GGGAAGGGAATGGAA[A/T]GGAAGAAAGGAAGGA	10529
rs372822742	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20996303	TCCAGAATGCTTTTT[C/T]ACTTGCAATTGCCAT	10529
rs372829150	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20974434	AATTTTTGTATTTTG[C/T]GTAAAGATGGGGTTT	10529
rs372835649	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21103426	CACCATGTTAGCCAG[G/T]ATGGTCTCCATCTCC	10529
rs372837664	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21094209	TAGAAATATAAAAAT[A/T]AGCCAGGTGTAGGCC	10529
rs372838037	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21149402	TTCAAGCGATTCTCT[C/T]ACCTCAGCCTCCTGA	10529
rs372840923	in-del	-/CAAA			intron-variant	NEBL	GRCh38.p7	10:20966705	AAGACTTCTGAAAAA[-/CAAA]ATAACAGGCAGAGTG	10529
rs372842924	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20947274	GAGCATTAGGGGAGT[C/T]GTAGGGTAACTTTCA	10529
rs372861201	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20803808	TCTTTCCTTCTGTAC[A/G]AAAAATATATATATA	10529
rs372869774	snp	C/T			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21139787	TAGAAATGCCGAAGT[C/T]TATGAAAGCCACAGT	10529
rs372876090	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:20904048	TCATAGCAAGAGAAC[A/T]ACTAGTAATAAAATA	10529
rs372876689	snp	A/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20873745	TTTTCTTATTTTTAT[A/T]AGAATAATTTTAGTC	10529
rs372876854	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20881360	CATTAAGTGCACAAA[C/T]CTTTGGGAGAAAATA	10529
rs372893611	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20886351	AACATGGCGAGACCC[C/T]GTCTCTACTAAAAAA	10529
rs372895899	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20966011	GTCTTATCTCCCTAC[A/G]GTCTTATCCCTTCAA	10529
rs372898663	in-del	-/T	0.00119737	0.0244387	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20881143	AAGATGAAATTTCCA[-/T]TTTTATTCATCTAGC	10529
rs372903318	snp	A/C			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20853296	TTTGGACATATAGAC[A/C]AAAAGTTGAATTTGG	10529
rs372909923	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:20885800	TTTTTAAAGTGACCC[A/T]CATTATCAGCAAGTG	10529
rs372924804	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20836283	GCTGGAGTGCAGTGG[C/T]GTGATCTCGGCTCAC	10529
rs372933543	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21112133	AGGAATGCTTTTACA[C/T]GGTTGGTGGGAGTGT	10529
rs372934691	snp	A/G			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20854210	TTATTAGACAATGGG[A/G]TACCAGTAAAAATGG	10529
rs372935378	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:20981409	ACTGCATCTCATAAA[A/T]AAAACACACACAAAA	10529
rs372937372	snp	A/G			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20864435	AGTTAATATAAGAAG[A/G]GTTTGGTATGTGTTC	10529
rs372938074	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20871971	AACAAACCCAAATTA[C/T]CACCCACCTACAAGA	10529
rs372941996	in-del	-/GTTGTTGTT			intron-variant	NEBL	GRCh38.p7	10:21122033	GTTGTTGTTGTTGTT[-/GTTGTTGTT]TTGAGACACAGTCTC	10529
rs372946100	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:20932438	GGGGTGGGGGAGAAA[C/G]GGGAGGGAGAGCATT	10529
rs372950954	snp	A/G			intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20958318	TATGCCCTAGAGTTT[A/G]GGGGCAAGGAGAGGG	10529
rs372970065	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20807290	GAGATTGTGCCACTG[C/T]ACTCCAGCCTGGGCA	10529
rs372970750	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21096557	CTCAGTCTGTCACCC[A/G]TGCTGGAGAGCAGTG	10529
rs372987856	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21161425	AAAGAACTCACCATG[A/C]CCCCAACAAAGCTAG	10529
rs372989051	snp	C/G	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:20942391	GGCTAGCCATATGTA[C/G]AAAGCTGAAACTGGA	10529
rs372993528	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21154317	TACAAAAATTAGCCA[A/T]GCATGGTGGCATGTG	10529
rs372995236	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20814625	ACACACATACACACA[C/T]ACACACACACACACA	10529
rs372997114	snp	A/C			intron-variant, upstream-variant-2KB	NEBL, LOC102725112	GRCh38.p7	10:20845528	GTTCAACTTTGTCAT[A/C]AATTTTAGAATTCTA	10529
rs372999701	snp	A/C/T	2.15357e-05	0.00328137	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20785710	AGATTAGGTTTGGGA[A/C/T]ACATTAGAATAAAGC	10529
rs373008496	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20937480	CAAGATGGTCGAATA[C/G]GAACAGCTCCAGTCT	10529
rs373031513	snp	C/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20860676	AGTAAGCTGTTTTGT[C/T]CTCTCATAATATTTT	10529
rs373031897	snp	C/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20849071	ATGCCTAGCATGAAG[C/T]ATCAAGGTTGTATTG	10529
rs373038719	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:20795504	ACTTTTAGATTTATT[G/T]TAAGAGTCATTTTAG	10529
rs373040845	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20801025	GGTTCAGCACTGCCC[A/G]TGCTCTAGTTCCAGA	10529
rs373043594	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20972225	TCTCAAAGTCTCGTC[A/G]CAGCTGATAAAAGTG	10529
rs373055910	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21011812	CTCCCCACCTGCACA[A/T]CCACCCCTGGCCCCA	10529
rs373069314	snp	A/G	3.30049e-05	0.00406219	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20785918	GTACATGGCTCGGTA[A/G]GTCCTCTGAGAAAGG	10529
rs373074959	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20970335	CTTCAGTCCTTTTTG[A/G]ATCAAAAAAAGAATA	10529
rs373082901	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20832108	TTAAATAAATCATTA[C/T]TCCCTTCACTGGCTC	10529
rs373086685	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21095330	CTAGCCTAAGAAAAG[A/C]AGATAAAAGATAAGA	10529
rs373103270	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21020732	CCATCTTGAAATGTC[A/G]TCTCCCCGGGTTTAC	10529
rs373122561	snp	A/C			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20868211	TCTTTGATAAGACTT[A/C]AAAGTTTTCTTCATT	10529
rs373126112	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:20971664	TGTCACCCAGGCTGG[A/T]GTGCAGTGGCGCAAT	10529
rs373129570	snp	C/T	1.66452e-05	0.00288484	intron-variant, missense, nc-transcript-variant, upstream-variant-2KB	NEBL, LOC102725112	GRCh38.p7	10:20845355	TCCTTCTCAAAATCC[C/T]CTTTGTAAACTTTCT	10529
rs373130227	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20831892	TTGGGTCATATATGG[C/T]TTAGTTAAGTGTCAG	10529
rs373134143	in-del	-/CTC	0.00517822	0.0506191	intron-variant	NEBL	GRCh38.p7	10:20906861	AATCTCTAACTTTCT[-/CTC]CTATTTCAATCATAC	10529
rs373156103	in-del	-/GTT			intron-variant	NEBL	GRCh38.p7	10:20819734	GTTGTTGTTGTTGTT[-/GTT]TTATTTTTGAGACAA	10529
rs373167913	snp	C/G	1.65111e-05	0.0028732	intron-variant	NEBL	GRCh38.p7	10:20785933	GGTCCTCTGAGAAAG[C/G]AAGAAGGGATTATAC	10529
rs373168039	snp	A/G	0.000118146	0.007685	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20868810	TATTTCTACCCTCCA[A/G]TGATGAACTACATTG	10529
rs373187661	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:20893841	AATAATTCAAACTAT[A/T]ATTTAAAGATGATGG	10529
rs373196764	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20947969	CCACACAAAAAAATA[C/T]GTTAACACTAACAAA	10529
rs373199762	snp	A/G	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:21044329	TTGAACCCGGGAGGC[A/G]GAGGTTGAAGTGAGC	10529
rs373200458	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20833651	TCAAGGATTCTTCTC[C/T]TGCTGGGTTAAGAAT	10529
rs373203856	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:20988392	ATTTTACTGGAAAAA[-/A]TGGGACTACTTAGAA	10529
rs373209242	in-del	-/AAAAAA			intron-variant	NEBL	GRCh38.p7	10:21113290	AAGGATGAGAATCCT[-/AAAAAA]AAAAAAAAAAAAAAA	10529
rs373218915	snp	C/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20856365	AGTGGCACGCTTTCT[C/T]CCAGCCACCAAATGT	10529
rs373219650	snp	A/C	1.72472e-05	0.00293654	intron-variant	NEBL	GRCh38.p7	10:20889807	TATAATAAGAAAAAG[A/C]TAAATGCAAGCCAGT	10529
rs373220310	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21081590	GAAGGTCCAGGAGCA[A/G]TGACACTCCAATAGC	10529
rs373241569	snp	A/C/T	6.62771e-05	0.00575628	intron-variant	NEBL	GRCh38.p7	10:20831433	TCCAGCTATGATTCA[A/C/T]GGCATTTATTTTAAA	10529
rs373243704	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21079429	GACCTTGTTTTGGAA[A/G]TGAGAAAACTCAGGC	10529
rs373244101	snp	C/G	0.000148907	0.00862735	intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20831200	TCATGACCAACCTGG[C/G]TATAGATTTCAGATG	10529
rs373249774	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:21086628	CTAAAAATACAAAAA[-/A]TTAGTCATGTGTGGT	10529
rs373282016	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:20904649	TCACATGTGTGCTTG[G/T]ACATATGTACATTCA	10529
rs373283147	in-del	-/AC			intron-variant	NEBL	GRCh38.p7	10:20963003	AAGCTTGAAAGAAAA[-/AC]ACACACACACACACA	10529
rs373284778	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21047819	TAAAAGCAACCGGAA[C/T]CTTCCCCGCATGCCC	10529
rs373311741	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21111380	ACAGGCTGGTACTGG[G/T]ACCAAAACAGATATA	10529
rs373315909	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20796236	GGCGTAGTGGTGGGC[A/G]CCCGTTATCCCAGCT	10529
rs373319913	snp	A/G			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21145664	ATTAAAATCCAAGGA[A/G]GTTATGACCTGCCGA	10529
rs373326775	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20967835	TGCATGTACACATTA[C/T]ATATAATCTTTTGTG	10529
rs373342123	snp	A/C/T	9.00575e-05	0.00670981	intron-variant	NEBL	GRCh38.p7	10:20812985	TTTGCGGATAGTTAC[A/C/T]TCTTTCACAACATTT	10529
rs373342370	snp	C/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20880675	CTGACTGATAAGAAA[C/T]ATTAAAGTCTTTTTT	10529
rs373343854	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21039945	GTAGACCGTGACATG[G/T]GGGATGATCCTTTTG	10529
rs373360265	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21167605	GAAATTTTAAGAACC[A/G]ACGTATATTTTAAAA	10529
rs373389771	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20806954	GTTTTATTTATCTCT[G/T]TAAATATCAATATTA	10529
rs373407564	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20965590	ACACGGGGCTTTGCA[C/T]GCCCTGAGGATGTTG	10529
rs373412117	in-del	-/TA			intron-variant, downstream-variant-500B	NEBL, LOC102725112	GRCh38.p7	10:20885069	TTGACTTTAAGATAA[-/TA]GTTTGTTTTAATAAT	10529
rs373417418	snp	A/G			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21136003	ATTTCTCAAAGAGAG[A/G]AAGCCCTTCTTCAAT	10529
rs373426552	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20991263	ATAACTGTCAAGCCC[C/T]CAAAAAAAAAATGCT	10529
rs373428265	in-del	-/A			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20866405	ATCACGATAAAAAAA[-/A]TGGGGAAAAATTACA	10529
rs373449187	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20825699	ATGTACTAAATATAC[A/G]TGGGAGAATATCAAA	10529
rs373451127	snp	A/C			upstream-variant-2KB, nc-transcript-variant	NEBL, NEBL-AS1	GRCh38.p7	10:21174679	AGATCCGCGGGGAAC[A/C]CGGAGACCTGCGTCC	10529
rs373462989	snp	C/T	0.00517822	0.0506191	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20858169	AAGCAGGTGAGCACA[C/T]GAACGCTGCAGACAT	10529
rs373467309	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21163034	TCCTTAATCCTAAGA[G/T]ATAGAGTCTATTATA	10529
rs373474665	snp	C/G	3.49565e-05	0.00418055	intron-variant	NEBL	GRCh38.p7	10:20828512	GGTGGCAACTTAAAA[C/G]AAGTAATGGCTACTC	10529
rs373477985	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21158879	TTCTGTCATCGTTTA[C/T]TATCACAATTATCCT	10529
rs373483826	snp	A/G			utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20782773	AAGTGTGTAAACAAT[A/G]ACAAGAAGACATGAA	10529
rs373486422	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21050517	GAAACACAGCCTTTG[C/T]CTGCAAAGAAGCAGA	10529
rs373487573	snp	A/G	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21040235	GCTGGGTATGGTGGC[A/G]GGTGCCTGTAATCCC	10529
rs373507766	snp	C/T			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21129235	CATTTTTTTAAAAGG[C/T]GTAAGTAGAGGTAAA	10529
rs373511767	snp	A/C/G			intron-variant	NEBL	GRCh38.p7	10:20930589	CCTACTAAATCCTAC[A/C/G]CCAGTTCCCCTTTTG	10529
rs373525896	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20842728	AATATTTACTTTTTC[A/G]TGGCGAGAACATTTG	10529
rs373527846	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20790267	AACCTAGTTATCTAC[C/T]TTATACTTGGTACAA	10529
rs373538681	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:20976923	CCTGAATCTACATTA[-/A]AAAAAAAAAAAAAAA	10529
rs373553375	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21019785	CCTTGTTTTTCCCCA[C/T]ATATGCGGTGTGGAA	10529
rs373554716	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:20991264	AACTGTCAAGCCCTC[-/A]AAAAAAAAAATGCTA	10529
rs373558661	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:20827612	ATTTATTAATGGACT[C/G]AGCCTCTTAATTAAT	10529
rs373564574	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20993856	TGATCTGGGGCACTG[C/T]CACCCTAACTAACTC	10529
rs373589431	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20834120	GAACACTTAATTTTT[C/G]TATAAGAATGAGGTA	10529
rs373591934	snp	C/T	3.64518e-05	0.00426902	utr-variant-3-prime, intron-variant	C10orf113, NEBL	GRCh38.p7	10:21125794	TTTTATTGTATATGG[C/T]ATGGTATAAGACAGT	10529
rs373600904	in-del	-/A/AA			intron-variant	NEBL	GRCh38.p7	10:21007121	TACAGAAAAAAAAAA[-/A/AA]CTGTTCACAGAATTT	10529
rs373617362	snp	A/C			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20877712	AGACCCCATTTGCAT[A/C]ATATAATTAGGGCGG	10529
rs373621973	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20783368	AACTACCCTTTAGTT[A/G]AATTCTGATCAGATC	10529
rs373622081	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20790704	CAATTTAAGAAGAGG[C/T]ATAAACACTGCTTTT	10529
rs373635568	snp	C/T	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20934943	GGTCAAGAGTTGTGA[C/T]TGGAAATGAATCTGG	10529
rs373657330	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20903184	ACCTATGATAAAGTT[C/T]AATTTATAAACTAGG	10529
rs373665749	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20887675	GCCCACCTTGGCCTC[C/T]TGAAGTACTGGGATT	10529
rs373676904	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:20929316	TTCAATAGACTTATT[C/G]ACAGCTATTAAGTAT	10529
rs373691801	snp	C/T	0.00557542	0.0525036	intron-variant	NEBL	GRCh38.p7	10:21067262	AGGTGTGAGCCACCG[C/T]GCCCAGCCGAAATAA	10529
rs373699154	snp	C/T	0.000131828	0.00811768	NEBL	10	allele_origin=T(germline)/C(germline)	10:20835499	TTAAGGCCTGCATCA[C/T]GCACCCTACTAACCT	10529
rs373705013	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21169071	AAAAAAAAAAAAATA[A/T]ATATATATATATATA	10529
rs373706874	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20975312	AGTGTTTCGACTTCT[A/C]TTAAGAATCCTAATT	10529
rs373709698	snp	C/G	0.000153988	0.00877328	intron-variant	NEBL	GRCh38.p7	10:20896916	CATAATAATACCACA[C/G]GTGCAATGCAAAATA	10529
rs373712288	snp	G/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20884296	TGCCCAGGCTGGTCT[G/T]CAACTCCCGGGCTCA	10529
rs373718699	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20891922	TATTAGATACATATT[A/G]GTAGCCTTCCTACAC	10529
rs373721327	snp	A/G	1.65518e-05	0.00287674	intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20809821	CAGAGAGCATATGGA[A/G]ACTTCTAGACTGAAT	10529
rs373730822	snp	A/C	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:21014890	CGTACTTCCTATGAA[A/C]CACGTTTTCATGCCT	10529
rs373732472	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20971356	TTTGCTTCTGAACAC[A/G]TGTTCTCTTAATCCT	10529
rs373746635	snp	C/T	0.0119091	0.0762411	intron-variant, upstream-variant-2KB	NEBL, NEBL-AS1	GRCh38.p7	10:21173483	CTGGTCCCTCCGGGG[C/T]CCGGGGCTGCGCACC	10529
rs373748632	snp	C/G	0.00013957	0.00835257	intron-variant	NEBL	GRCh38.p7	10:20828515	GGCAACTTAAAAGAA[C/G]TAATGGCTACTCACC	10529
rs373760385	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20925585	GACTTACCTTATTCT[A/G]AAAGAAAGCAATCTG	10529
rs373770486	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20830188	CCCTTTTGAACTAGT[A/G]GATGGTTAATGTCCT	10529
rs373776798	snp	A/C			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20873367	AAATCATCAACTCAG[A/C]AGAGATGTGAACTTG	10529
rs373777827	snp	C/G/T			intron-variant	NEBL	GRCh38.p7	10:20805565	ACCCCAAAGAGTCAA[C/G/T]TTTTTGGCCAGGCAC	10529
rs373779476	snp	C/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20847805	GCCTCAAGAATATTC[C/T]TGTCTCTAATCCTAA	10529
rs373784448	snp	C/T	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:21031094	GACAATGGCTGTCTT[C/T]GTGGATGTCTGTCCC	10529
rs373787064	in-del	-/T			intron-variant	NEBL	GRCh38.p7	10:21104626	AGTTGATTTTTTTTT[-/T]CAGATTCCCTACGAT	10529
rs373788661	snp	C/G	1.67764e-05	0.00289619	intron-variant, upstream-variant-2KB	NEBL, NEBL-AS1	GRCh38.p7	10:21173739	CGCCCGGCAGGTCCA[C/G]GCTGGCCCGGCGCCC	10529
rs373809133	snp	A/G			intron-variant, upstream-variant-2KB	NEBL, NEBL-AS1	GRCh38.p7	10:21172934	TATGTAAGTACCCCT[A/G]CACCTGACCAGCTTC	10529
rs373810818	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20952831	AATTACTTGAACCCC[A/G]GAGGTGGAGGTTGCA	10529
rs373813159	snp	A/G	0.000117207	0.00765439	intron-variant, upstream-variant-2KB	NEBL, LOC102725112	GRCh38.p7	10:20845254	ATAAACACCAAGATC[A/G]TACCTCCCTCAGAAG	10529
rs373817028	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:20948328	GATCAGAATCCAATA[G/T]GCTAGTCAGTTTACT	10529
rs373820934	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20878218	CTGCTTACTCACATT[A/G]CTAAAGGCACAAGAG	10529
rs373826045	snp	A/G	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21140208	GTGTATGGAATGGTT[A/G]AGAATCTGATATCTT	10529
rs373826825	snp	A/G	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:21170575	TCATTTTTGCTTCAC[A/G]CTATTCCAATAGGAA	10529
rs373843402	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21067369	TTGAGCCTTCAAACT[A/G]TAATTCATTAAGAAA	10529
rs373862825	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21082330	GATTAGATCACAGTG[A/G]TAAATAAATATTAGT	10529
rs373868280	snp	C/G			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21142210	CTTAAAATATGCCAG[C/G]CTTTCTCAGAGACCA	10529
rs373869641	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20915177	GAAAATAAATGAACC[C/T]ATCACTGTAATAACA	10529
rs373873210	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20821327	AATTTAGGTTTCAAG[A/C]GGTGAATGGCTTACA	10529
rs373873697	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21151417	AATGGGATATCATTA[C/T]AGTAAATATGTGACT	10529
rs373892146	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21028219	CCAACAGAGCGAGAC[A/T]CCATCTCAAACATCT	10529
rs373901453	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21045632	ATGCTCAACATCACC[A/C]ATCATCAGGGAAATT	10529
rs373905214	snp	C/T			utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20781236	TTAGTAACATTGTAA[C/T]ATTCCGTGAAGCCCC	10529
rs373905298	in-del	-/GAAAA			intron-variant, downstream-variant-500B	NEBL, LOC102725112	GRCh38.p7	10:20880379	GAAAAGAAAAGAAAA[-/GAAAA]CAGTAGTGGGTACAA	10529
rs373910526	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:21166844	TAGCAGGAATTTCAT[C/G]AATCTCCTTGAGATA	10529
rs373943279	snp	C/G			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21133408	TTACAATTTCTCTAT[C/G]ATTCCCCAATCAGTG	10529
rs373946202	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21025718	TGCCTGGGTTTGTAC[G/T]TGGCTTGTCTACCTT	10529
rs373949864	snp	C/T	0.00716266	0.059414	intron-variant	NEBL	GRCh38.p7	10:20790053	TGCTACTGTTAAATA[C/T]AGCAAGAAAAGAAAG	10529
rs373950695	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21015801	TACAGGCATAAGCCA[C/T]AGCACCCGGCTAGAA	10529
rs373967333	snp	A/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20799454	CCCGGTTCATCACAG[A/T]CATTTAGTATTTCAA	10529
rs373968420	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21099785	CCTTGAATGTTGCAG[A/T]TCAGTTGCAAGTGTT	10529
rs373982663	snp	A/G	0.00119737	0.0244387	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21140134	CCACTACACTTCAGC[A/G]TGGTCGACAGAGCGA	10529
rs373986849	in-del	-/TC			intron-variant	NEBL	GRCh38.p7	10:20992764	TTTGCAACTACAAAG[-/TC]TTTTTTTTTTTTTTT	10529
rs374002264	snp	C/T	0.00159617	0.0282053	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21132825	TATTTTTAATTGGGT[C/T]ACTTGTCTTTTAATA	10529
rs374005089	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21046026	ACACACACACACACG[C/T]GTGTGCACTGGAATA	10529
rs374011957	snp	C/G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20969340	GCATTAAAAATCATG[C/G/T]CCATAGATTTCTAAG	10529
rs374012321	in-del	-/TACG			intron-variant	NEBL	GRCh38.p7	10:20822678	TATAGAGACTATAGA[-/TACG]TATATAGATATATAG	10529
rs374027108	snp	C/T			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21126254	ATCCATCTTCAAAAT[C/T]AGGGACTTCTTTTGT	10529
rs374032261	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21113311	AAAAAAAAAAACCAG[A/G]AAAAAACTCCTAAAA	10529
rs374038771	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21152764	TTTCTGTTTGGAGAG[A/C]AAAGAAAGACTAATG	10529
rs374045262	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21115906	TGGGCTATTTTCTAC[A/G]GTCCCACTACTCACT	10529
rs374056224	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:21025765	GGGTTAGGTTTCTTA[-/A]CCTCTCTGGCCTCAA	10529
rs374073327	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:21032141	CCATCAAATGTTTTA[-/A]GTCTCATGATAACAT	10529
rs374075372	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20901812	TCCCTAGTCATTCCA[C/T]CTTTGCCTCACCTAT	10529
rs374081573	snp	C/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20847501	TTATAAGTTTCTGGA[C/T]TTATCAGTGAAAGGA	10529
rs374083192	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20959760	TGCTACGGCTGCTAA[C/T]ATTAAGACATCGCAA	10529
rs374088031	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21022408	GCCTACCCAAAGCAC[G/T]CTAGCACTTGCGAAA	10529
rs374092177	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21012416	CCAGGCTGGAGTGCA[A/G]TGGCATGATCACAGC	10529
rs374100641	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21033727	CCTGGCAACAAGAGC[A/G]AGACTTTGTCTCCGA	10529
rs374108482	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20930112	CACTAGTAGAGAGAA[C/T]AGCTTAACGGCCACC	10529
rs374115918	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:20792081	GGTTTTGAAGGCCCC[A/T]CAATGACTATAGAGA	10529
rs374141524	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21121403	AAATAAAATCAAGAT[A/G]ATATTTATTTTAGCT	10529
rs374147107	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20840469	TCATCTGCCTTTTAC[C/T]TGCTTAAAAGATGAA	10529
rs374154151	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21028242	AAACATCTCAAAAAA[A/G]AAAAAAAAAAAAAAG	10529
rs374158464	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21117904	TAACCTGAGTCCACC[C/T]GATCTATAAAAAAAG	10529
rs374163745	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20801886	AACTGCTACAAAATT[A/C]AGAAACTTACTTTCA	10529
rs374167218	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20905456	GAGAGAGCCAGCAAG[A/G]GCAGGGAAAACTGCC	10529
rs374171919	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21115030	TTATGATTCCTTTTT[A/G]TCTTCTTTATTGGCT	10529
rs374173003	in-del	-/A			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21135448	ATAAAAAAAAAAAAA[-/A]TCTGGCAATGATGCT	10529
rs374183778	multinucleotide-polymorphism	AA/GG			intron-variant	NEBL	GRCh38.p7	10:20999162	CAGAGGTGTGTGGGG[AA/GG]AAAAAAAAAAAAAAA	10529
rs374186645	in-del	-/T			intron-variant	NEBL	GRCh38.p7	10:21041649	CTCTACTCTTTTTTT[-/T]ATTATTATTGAAAGC	10529
rs374217764	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20810199	TCACACAACACAGGA[A/G]CACATGGGGCAGCTA	10529
rs374218305	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21072490	AGCCACCAACAAAAT[A/C]TTCTGGAACAAGTGG	10529
rs374218451	snp	A/G	4.94743e-05	0.0049734	intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20889885	TTTACATGGTTTAGC[A/G]TAGGACTGTCAGTCA	10529
rs374220897	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20994572	TGAAGAATGCAGGCA[C/T]TAAGGGCATTGACCC	10529
rs374227893	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21078683	AGAAAAATCATGTAT[C/T]CAAGCTCTACAACAT	10529
rs374233691	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20893878	AGCTATCAGCTACAG[G/T]TCAGAAATTAGGAAT	10529
rs374242976	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20879376	TTACAGTCATCCTTA[A/G]GCAAACAGTTCTTAT	10529
rs374250519	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20955466	AATTGTCCTAAACAT[A/G]CAGAATGACTCATGC	10529
rs374278505	in-del	-/AGT	0.00199481	0.0315187	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20866106	GTTAACATGGCAAAA[-/AGT]AGTTCTGATGTTTAC	10529
rs374295833	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21050247	TTTACTTTTTCTGTA[C/T]TCTCACGGAAACTAT	10529
rs374314938	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20808036	CCCAATTTCTTTTGG[C/T]AAGGTCTAACTCTGT	10529
rs374317504	snp	C/G			intron-variant, upstream-variant-2KB	NEBL, LOC102725112	GRCh38.p7	10:20843854	AAATCCTCTCTTCTA[C/G]CTTATTAAAAACATC	10529
rs374319299	in-del	-/C	0.00478085	0.0486577	intron-variant	NEBL	GRCh38.p7	10:21123813	AAATATACATAATCT[-/C]CAATTGGTTGTATAT	10529
rs374330420	snp	C/T	8.24926e-05	0.0064218	intron-variant	NEBL	GRCh38.p7	10:20835644	AAAGACAACATTTTA[C/T]AACATTCAAACACTC	10529
rs374330746	snp	C/G/T	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20812200	GTCAACAGAACAACA[C/G/T]GTCAACCAAGCAGAA	10529
rs374336095	snp	G/T	1.6476e-05	0.00287014	missense, intron-variant, utr-variant-3-prime	C10orf113, NEBL	GRCh38.p7	10:21125933	CTGGTCCCAGAGACA[G/T]CCTTGGGGACTTGGC	10529
rs374337490	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:20887390	AATTGATGAAGCAGA[A/T]CTGTGGATCCTGAAT	10529
rs374337821	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21047112	ACTGAAAGTCAATCA[C/T]TGACTTCCTGATAAT	10529
rs374344424	snp	A/G	3.29832e-05	0.00406085	intron-variant, synonymous-codon, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20869788	CTTGATGTCTGGTCG[A/G]TCAAGTTCTGCACTG	10529
rs374344929	multinucleotide-polymorphism	GG/TA			intron-variant	NEBL	GRCh38.p7	10:20929764	GTGGGGAGGGTGGGA[GG/TA]GGATGACAGATGAAA	10529
rs374356062	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21041603	TAAAATCACTAGAAG[A/G]ATAGTTAGATATACA	10529
rs374359719	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21041311	AACATGCGGTATTTG[G/T]TTTTCTGTTCCAGCT	10529
rs374361615	snp	C/G			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20862459	TGCAGGTAAAATGAA[C/G]TAAGATCACCAAATG	10529
rs374371449	snp	A/C	0.00557542	0.0525036	intron-variant	NEBL	GRCh38.p7	10:21075210	CCCACGGTGGAAACA[A/C]AATGGTAATATTTTG	10529
rs374371953	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20796364	AAACTCAGTCTAAAA[A/C]AAGAAAAAAAAAAAA	10529
rs374376752	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21057247	CCTGGTTGGGAGAAC[A/G]GTCTCCCGGGAAGGG	10529
rs374378901	snp	C/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21064490	GCTCTAACTCAACCT[C/T]CAGAAAAAATGAGCA	10529
rs374380453	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:20902035	ATAGCTATTTCATTA[C/G]TCTTTAATAATCAGA	10529
rs374389652	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20828759	GTTTTTACTGACTTA[C/T]ACTCCCAGAGAGAGA	10529
rs374406935	snp	C/T			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21143892	AGCTTAAAATAAGAC[C/T]ATTCCAGAAAAACTT	10529
rs374410634	snp	C/T	1.64808e-05	0.00287057	intron-variant, missense, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20880799	GCTTCCTTACATTAC[C/T]CTGGTGTTTATTGAC	10529
rs374413743	snp	C/T	0.00478085	0.0486577	intron-variant	NEBL	GRCh38.p7	10:21171692	TTGACACACGGTGAG[C/T]GCGATATAAATGCTA	10529
rs374416141	in-del	A/GG			intron-variant	NEBL	GRCh38.p7	10:20994886	GAGGAGGAGGTAGAG[A/GG]GGGGGTTGGTCTTGC	10529
rs374418440	snp	A/G			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20853159	GCACAAGGAAAATGT[A/G]AGAGAAATAAGCAAC	10529
rs374421663	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20889608	GTATATAAATAAGAA[A/G]GATTTAGAGTCAAAA	10529
rs374426179	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21155626	GGTAACATTTCAACT[C/T]TCAAACTCACATTCA	10529
rs374443517	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20991272	AAGCCCTCAAAAAAA[A/G]AATGCTATTAGCTTG	10529
rs374448077	snp	C/T	1.70211e-05	0.00291724	intron-variant	NEBL	GRCh38.p7	10:20814086	AATGATAAGAAAACA[C/T]ATGATGTAACATTTT	10529
rs374451899	snp	A/G	6.60012e-05	0.00574423	intron-variant, synonymous-codon, nc-transcript-variant	NEBL	GRCh38.p7	10:20808568	GCTAGGGTAAATCTC[A/G]GAGATTTCTGACCTG	10529
rs374452150	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21041128	GACTGTATGTCATGG[A/G]GGTTTGGTGTACAGA	10529
rs374453075	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21124965	ACTACATCTCTAAAA[A/C]AGAAAAAGAAATAGA	10529
rs374457822	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:20924399	ATGCCTATAGCTCTC[C/G]ATCAGGCATGAAGTA	10529
rs374459752	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21097331	AGGTATGGTGGCGGG[C/T]GCCTGTAATCTCAGC	10529
rs374468821	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21066762	GTCAAATGCATATTA[A/G]AATCTTAATTCCCAT	10529
rs374474317	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21098220	CACACACATTCTCAC[A/T]CACACGTGCACACAT	10529
rs374474935	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20903595	AGCACAATTCGCAAT[A/G]GCAAGGATACGGAAC	10529
rs374483805	snp	A/C	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20911480	AACTAACCAGGTATG[A/C]CTGAATGGCCAATAA	10529
rs374488018	snp	C/T	1.66358e-05	0.00288402	intron-variant	NEBL	GRCh38.p7	10:20831182	GATTCTGAGCATCTT[C/T]ATTCATGACCAACCT	10529
rs374489588	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:20892808	GTTTGCGGATCTTTC[C/G]TTTCACAAGAATTCT	10529
rs374490532	snp	A/C	0.000153988	0.00877328	intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20808633	AATGGGATCGAGACC[A/C]GTGTCGCCTATAGTG	10529
rs374492748	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21148788	GCCTCAGCCTCCCAA[A/C]GTGCTGGGATTACAG	10529
rs374496690	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21168771	GGCTCAACAGTGGCC[G/T]GGCGCGGTGGCTCAT	10529
rs374501176	snp	C/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20847323	ACATCTAATAGTCAA[C/T]GACTATAATTAAAGG	10529
rs374510578	snp	A/G/T	0.000148447	0.00861404	synonymous-codon, missense, intron-variant, utr-variant-3-prime	C10orf113, NEBL	GRCh38.p7	10:21126017	TGAAGCTGACTCTCC[A/G/T]CAGCCACCTGGCAAG	10529
rs374517621	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20906748	CAAATATAATTCAAC[A/G]AATTTTACTTGTTAA	10529
rs374525691	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21170461	ATCCCGTTTATGGGT[A/G]CTTGGGGCCCTTTCC	10529
rs374529495	snp	A/C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21116477	AAAGTGTCCATCTCC[A/C/G]ATTATCATCACATTA	10529
rs374532763	snp	C/T			intron-variant, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	NEBL	GRCh38.p7	10:20958906	CACACCTCAGTAACA[C/T]GCAGACTGAGTGGTC	10529
rs374562139	snp	G/T	0.000798403	0.0199641	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21133683	GTTATTATCAGGAAA[G/T]ATCCCATCATATCAA	10529
rs374565548	snp	A/C	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20917806	ACTTTCAAGATACTT[A/C]TTTGAGAAGCCAAGA	10529
rs374573842	in-del	-/AAAT/AAATAAAT	0.0527055	0.154702	intron-variant	NEBL	GRCh38.p7	10:21023696	GAGACTCCATCTCAA[-/AAAT/AAATAAAT]AAATAAATAAATAAA	10529
rs374590716	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:21152862	TGACCTTGAAAAAAA[-/A]CAACTGTACATCAAT	10529
rs374595892	in-del	-/TCTAAGGTACTGAGA			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20870679	CCCATGCCTAGGAGA[-/TCTAAGGTACTGAGA]GCTTTATCACCCAAT	10529
rs374598650	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21073128	GAAGGCCTGCTAGGA[C/T]CACTCAAGAAGTGTG	10529
rs374601034	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20934979	AACTGGCATGCTGTG[C/T]AATAGTGAAGCAAAG	10529
rs374601910	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21099245	TAAACTAAAAGTGAC[A/G]GGTATGAATTCAATG	10529
rs374601926	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:20893147	GTGGTCCACCTGCTC[G/T]GCAGAAGGCTCTTTC	10529
rs374619670	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21151218	TTGCACATATAGCAA[C/T]GCACACCATGTAATT	10529
rs374622104	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20946769	GTAATATAGTTCACA[A/G]TCTAAAAGTGGGGTA	10529
rs374659780	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	C10orf113, NEBL	GRCh38.p7	10:21147258	TCAACAAGGTCTCAT[G/T]GCACGTTAGCCATTT	10529
rs374661485	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21052365	AGCTAAGCTTTCCAC[C/T]TCAATTCTCCAACCA	10529
rs374676703	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21065971	CTTCAACCTGGTTAC[A/G]TGTTAGCTGTCCTCT	10529
rs374678979	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20933360	ATTTTCAGAAAATAG[C/T]CTCAAAACTTACCCG	10529
rs374705635	snp	C/G	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:20820598	TGGAAGGCCGAGGCA[C/G]GTGGATCAACTGAGG	10529
rs374708982	in-del	-/TG			intron-variant	NEBL	GRCh38.p7	10:20953528	TTTTTTTTTTTTTTT[-/TG]GTAGGCTCTTGGATT	10529
rs374710121	snp	C/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20850695	TAATATAAAATATCT[C/T]AAGGGATAAAAATAA	10529
rs374711781	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21095587	AGGATGTGATTTTAA[C/T]GTAAGTAGAGTCCAA	10529
rs374718322	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20956199	AAGAGGTAATTTTCC[A/G]TACATTTCTCACATG	10529
rs374729042	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:20798833	TCTTGGCACATCGAT[C/G]AAAGACACATGTGCA	10529
rs374762266	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20949734	GTTTGATTTCCTTTT[A/G]TGTTTTGTTTTTTTT	10529
rs374773045	in-del	-/T			intron-variant	NEBL	GRCh38.p7	10:21041649	TCTACTCTTTTTTTT[-/T]ATTATTATTGAAAGC	10529
rs374796648	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21018981	GCAGTGAGCCGAGAC[A/G]GCACCACTGTACTCC	10529
rs374805909	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21039587	AGATTCAAGAGAGAA[C/T]TAAATTATGTAAAAG	10529
rs374816761	snp	A/G	0.000163987	0.00905353	utr-variant-5-prime, upstream-variant-2KB	NEBL, NEBL-AS1	GRCh38.p7	10:21173883	TGCTGGCTCCCAGGA[A/G]CCGCTGTGACATCCC	10529
rs374823536	snp	C/T	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:21033693	TGCAGTGAGTCAAGA[C/T]TGCACCACTGCACTC	10529
rs374851899	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20953475	CTGCAATATCTTGTT[A/G]TGGTGCCTGAGCAGA	10529
rs374859608	snp	G/T			utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	NEBL, NEBL-AS1	GRCh38.p7	10:21174048	CTCGGGCTCGCAGGC[G/T]CTGGGTCTCGGCTCC	10529
rs374866342	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20929633	TGGAGGCCATTATCG[C/T]TAAGTGAAATAACTC	10529
rs374871950	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20791987	ACAGAGGCTGAGAGA[C/T]TGAACAGGAAGGCAG	10529
rs374880575	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21088425	GGAGTTCAAGGCTGT[A/G]GTGGGCTATGATGGT	10529
rs374884126	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:20952079	TCACTACACTCTAAA[-/A]GTATCTGTGTTTCTA	10529
rs374904057	snp	A/G	3.29489e-05	0.00405874	missense	NEBL	GRCh38.p7	10:21020175	GGTGTATCTGCCACC[A/G]TGGTGAAGGACTGCT	10529
rs374919853	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:20951129	AAACAAAAAAAGAAG[C/G]TGACTTTGTTACAAT	10529
rs374923937	snp	A/C	0.000153988	0.00877328	intron-variant, stop-gained, stop-lost, nc-transcript-variant	NEBL	GRCh38.p7	10:20815680	TCAGGAGTTACACTT[A/C]AAGTGGTAGCTCTTC	10529
rs374940171	in-del	-/GA			intron-variant	NEBL	GRCh38.p7	10:20937527	GTGACGCAGAAAACA[-/GA]TGATTTCTGCATTTC	10529
rs374957174	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21018834	GGAGTTCAAGACCAG[A/C]CTGACCAAGATGGTG	10529
rs374963694	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20838472	GGACAAGCAAAGAAT[A/G]TGGTTTCTGAAGATC	10529
rs374964974	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20839999	AGTAACTCAATCTTC[A/G]GATTTTCTATTCCAT	10529
rs374971466	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21070168	GGCCAGGACACTGGG[A/G]CTAAATACCCGGACT	10529
rs374972275	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20794954	GAGCTGAAGGTTAGC[A/C]GATTAAGTAATTTGG	10529
rs374972827	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21103314	CGCCTTCCGGGTTCA[C/T]GCCATTCTCCTGCCT	10529
rs374979602	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:21004357	ATTTTGGAAAAAAAA[-/A]TGCCAGGAGTGTTCA	10529
rs374992988	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21042518	ACTTCCTAATTATGT[C/T]ACTACGTGGTATTAT	10529
rs374997467	snp	G/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20882168	CAAGATCCTGCAAAA[G/T]AAAGAAAGAAGGAAA	10529
rs375001683	snp	A/C/G	0.000649789	0.0180131	intron-variant	NEBL	GRCh38.p7	10:20831167	GACATTGGAATACAC[A/C/G]ATTCTGAGCATCTTC	10529
rs375011018	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20939505	GTAAAGACCATCGAG[A/G]CTAGGAAGAAACTGC	10529
rs375019716	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:20815770	TCAATTCAACAAAGA[C/G]ACTTATTTATTTATT	10529
rs375023123	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21098168	AGGGCCCTTTCATGT[A/G]GGAGGATAGCAACAC	10529
rs375027575	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20892472	TGAACTACCTACCTC[C/T]GGGCTTTATATGTGG	10529
rs375032381	snp	C/T	3.38478e-05	0.00411373	utr-variant-5-prime, intron-variant	C10orf113, NEBL	GRCh38.p7	10:21146525	CTACTCCTGCATTAT[C/T]AGAAAATGGTGAAAA	10529
rs375036818	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20954724	CCCCCACCACCACCC[C/T]GCCCCCTCTGCAAAC	10529
rs375039212	in-del	-/GGTGCTAAGCA			intron-variant	NEBL	GRCh38.p7	10:20969019	GTTTGGTGCTAAGCA[-/GGTGCTAAGCA]TAGATTAAAAGCTTA	10529
rs375040586	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21004077	CTTATACGCATACAC[A/G]TAAGTACGTGTATAT	10529
rs375041567	snp	C/T	0.000263965	0.0114853	synonymous-codon, intron-variant, utr-variant-3-prime	C10orf113, NEBL	GRCh38.p7	10:21126024	GACTCTCCGCAGCCA[C/T]CTGGCAAGCGTTGGC	10529
rs375060837	snp	C/T			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21141971	CTTGACATAATACTA[C/T]ATCCTTCTAGGTAGA	10529
rs375064114	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:21160634	AAAGAGAAACGGAGA[C/G]ATAGTGGGGTTGGGG	10529
rs375079046	snp	A/C/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21063258	CTCCCTAGAGGCCCA[A/C/T]GTGCTCACTTGTCAT	10529
rs375086562	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20932008	ACCACTCACCCATTT[A/G]CTAGAAACAATATTC	10529
rs375108886	snp	A/G	1.64787e-05	0.00287038	synonymous-codon, upstream-variant-2KB	NEBL	GRCh38.p7	10:20961732	AGTGTCCGTGACGAT[A/G]CTGAAGCCCCTCCCT	10529
rs375110656	snp	A/C/G	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20800694	CGACAAATGCTCACA[A/C/G]TAAGAGAGGTTGCGA	10529
rs375117092	snp	A/G	0.000792066	0.0198848	intron-variant, synonymous-codon, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20852560	CTGACTTTGGAGGAC[A/G]GCATTGCCTTTATGG	10529
rs375129247	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21068610	GTGACACCTGACCAT[A/T]GACCCCGGACCCATG	10529
rs375129534	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20915195	CACTGTAATAACACT[C/T]CACCAACAAATACTT	10529
rs375138119	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20934544	CTGAACCTGAAACCC[A/G]TGCTATCCACGATGG	10529
rs375139653	in-del	-/TCT			intron-variant	NEBL	GRCh38.p7	10:20962210	AAAGCTAAATCTTCT[-/TCT]CCTCCTGTGCCCGCC	10529
rs375140844	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20935048	AAGGCCAATACATGC[C/T]AGGTACCATGTCTGG	10529
rs375143002	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20906425	AATTTATGAGCCTTA[C/T]TCCAATTATTTCCAT	10529
rs375145690	snp	C/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20859932	ATGAATGTTGCCAAG[C/T]GTAAATTCCTGGTAT	10529
rs375151481	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20831956	CTGTAGTGAATAAGT[A/G]TTGGTTGCTTCTCTG	10529
rs375154211	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:20892232	GGGGAGCCACACTCT[C/G]TGTGACTTTAGTGGA	10529
rs375155149	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20826895	ATATTACAAAAGCCC[A/G]TTAAGCCGTTATCAC	10529
rs375166381	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:20913009	TCAAATGATCCTCCT[G/T]TCTCAGCCTCCCAAA	10529
rs375169659	in-del	-/TACAGACTAGATG			intron-variant	NEBL	GRCh38.p7	10:20799053	TTCACAGGCTAGATG[-/TACAGACTAGATG]GTAAAATATAATCAT	10529
rs375179713	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21155251	AATGGGGTATCCATC[C/T]CCTCAAGCATCTATC	10529
rs375180443	in-del	-/AAAGT			intron-variant	NEBL	GRCh38.p7	10:21085748	TATATGTGTTAAAGT[-/AAAGT]TTTGTTCTAATATAA	10529
rs375185975	in-del	-/T			intron-variant	NEBL	GRCh38.p7	10:20953528	TTTTTTTTTTTTTTT[-/T]GTAGGCTCTTGGATT	10529
rs375190077	in-del	-/AT	0.0368353	0.130617	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20868848	CCAAAAAAAAAAAAA[-/AT]AACAGACCTTCATCT	10529
rs375191003	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21074483	TTTCTGAATTTTTTT[C/T]TTTTTTTTTTTTTTG	10529
rs375197621	snp	A/G	6.58989e-05	0.00573978	intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20819473	TCTATCTCCGGGGTC[A/G]TGCTTACCGGAGTGG	10529
rs375200389	snp	A/T			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21134677	CACAACTATTCCATC[A/T]ATTAGTGTATGTTTA	10529
rs375202194	snp	C/T	1.68289e-05	0.00290072	missense, intron-variant	C10orf113, NEBL	GRCh38.p7	10:21146362	CATGTCTGGAATGTA[C/T]ATTTCAGCCACACAA	10529
rs375203185	snp	C/T	0.00557542	0.0525036	intron-variant	NEBL	GRCh38.p7	10:21111591	ATACAAAAATTAATT[C/T]AAGTTGGATTAAAGA	10529
rs375206337	snp	C/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20886270	GCTCACACCTGTAAT[C/T]CCTGCACTTTGGGAG	10529
rs375208825	snp	C/T	0.000153988	0.00877328	utr-variant-3-prime, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20785761	ATTAATTAACAAACT[C/T]AATGTAATTCGCTGG	10529
rs375213792	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21088002	TATGTATCAGTCAGA[A/G]CAGGCTTGATTATGC	10529
rs375217640	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20997410	GGAAGTGGCCACAGT[C/T]ACCATTAGGTACCCC	10529
rs375223951	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21169115	ATATATATTTGGACA[C/T]ATAATTAGATCAAAA	10529
rs375241084	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:20800054	TAACTACAGTCCACA[G/T]GCTATATGTTACATC	10529
rs375252574	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:20789844	CAGAGAGCAATCTTA[A/T]CTCAAATTTTATATA	10529
rs375252960	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:21037192	AAATGAACAAGCAGC[C/G]AGCGACCATCCAGTC	10529
rs375265257	snp	A/C/T	3.29458e-05	0.00405857	intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20896998	CTGGCCAATTCCATG[A/C/T]TTAAGTCTTCAATAA	10529
rs375300198	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21161677	ATCTTCCCCAACTTC[C/T]ATTGACTGACTGGGG	10529
rs375314274	snp	A/T	0.00318978	0.0398085	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20860103	TTTTTAAATGTCAGT[A/T]TTCATTTCTGCATTT	10529
rs375316862	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20976734	TGAGAACACCTGGAC[A/G]CAAAGATGGGAACAA	10529
rs375318691	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20835236	CCATTAAATCTGTTG[C/T]ATTCTGAAATAAGGT	10529
rs375324537	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21110254	TTTTCCTTCAATCTT[G/T]GTTAGAACTCACCAG	10529
rs375325438	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21049397	TTCATTGTAGATTTG[G/T]GTGAGAACTTAGCAA	10529
rs375331043	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21112868	GCCTGTACATATTCA[C/T]AGACAGTATTTAGTA	10529
rs375332720	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21093084	GTTCTTGGCTTCTTG[C/T]GTATCTACCAAGGAG	10529
rs375333229	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21098116	GGCAAAAATGTGAGT[G/T]GATATGAATTTATAA	10529
rs375339505	snp	A/G			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20853647	AAAGAAATCAGCTGG[A/G]CATGGTGACATGCAC	10529
rs375346280	snp	A/T	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:20795332	CTATTTGTCATTAAT[A/T]TGTGTGTATATGTGT	10529
rs375350283	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20945981	CAAGTATTTCCAGGG[A/T]TTGTTGCTAAAAATA	10529
rs375356447	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21095329	TCTAGCCTAAGAAAA[G/T]CAGATAAAAGATAAG	10529
rs375364827	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20916596	TGTAATTTTAGTAGC[A/G]ACAAGGTTTCACCAT	10529
rs375378760	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20848752	CTCGCCAGTCCATGG[A/G]AAAATTGTCTTCCAT	10529
rs375381124	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20977797	CAACCACAGTTTGCC[C/T]TAATACGTTGCCAGG	10529
rs375381276	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20967412	GCAGGTGGATCACTT[A/G]AGGTCAGGAGTTTGA	10529
rs375383000	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:20933065	ACAAGTTTGCATGAC[-/A]AAAAAAAAAGGTACA	10529
rs375398750	snp	C/T	0.000153988	0.00877328	intron-variant	NEBL	GRCh38.p7	10:20897074	GAACATTTTTCTCAT[C/T]GTCAATTTAGAGGAA	10529
rs375411761	in-del	A/CC			intron-variant	NEBL	GRCh38.p7	10:21001506	AGGGAAAGAAACCCC[A/CC]AGGAACATCATGCCA	10529
rs375413744	snp	C/G/T	3.39593e-05	0.0041205	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20850527	AAAAAGAAAAGCATA[C/G/T]ACAAATCGAAAGTCC	10529
rs375414214	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21044135	GGCACGATGGCTCAC[A/G]CCTGTAATCCCAACA	10529
rs375436297	in-del	-/ATCCC			intron-variant	NEBL	GRCh38.p7	10:20922769	CACTCGAGCCATCCC[-/ATCCC]TTCCGTTGCTCCCCT	10529
rs375438276	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21048081	GTGAGCGGTTCTCCA[A/G]GACAAAAATTTCTGC	10529
rs375448864	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21061240	CATTATATATTGTGA[C/T]ATATTACATATTATG	10529
rs375455358	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20824292	GAAATCACCTGGTAA[C/T]GTTTAAAATGATTAA	10529
rs375457143	in-del	-/GAAAGAAAAGAAA			intron-variant	NEBL	GRCh38.p7	10:20820853	AAAATAAAAAAGAAA[-/GAAAGAAAAGAAA]AAGAAATAGACTTAA	10529
rs375470013	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20922642	AGCTGACGTGCTAAC[A/G]CAATGTAGGATAACT	10529
rs375500684	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21057639	ACGGCAACCTCTGCC[A/T]CCGAGGCTCGAGCAA	10529
rs375500989	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21092482	TTTGAAGTTCGTCTG[A/C]CCTGCCTATAATTTC	10529
rs375502547	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:20827657	ATTTACAATAGGAAA[C/G]ACATGGAATCAACCT	10529
rs375515042	snp	A/G	0.000798403	0.0199641	intron-variant, nc-transcript-variant	NEBL	GRCh38.p7	10:20819242	CGTCCAACAGGCTCC[A/G]GTGTCTGTTATTCCC	10529
rs375529925	in-del	-/GG			intron-variant	NEBL	GRCh38.p7	10:20981601	GATAACATGACTTGG[-/GG]GRCTGGCTAATCAGA	10529
rs375530888	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21118778	CCACTGATTAAGTTT[A/C]TCTTTCCTATGAATG	10529
rs375547683	snp	A/T			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21140819	AAGGGGAGGGAGAGC[A/T]TTAGGACAAATATCT	10529
rs375550299	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20894894	AGATCGTGCCACTGC[A/C]CTCCAGCCTGGGTGA	10529
rs375565296	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20984760	ACTGGTACCGGTCCA[C/T]GGCCTGCTAGGAGCC	10529
rs375569032	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:20886540	TCTTAAAAAAAGAAA[A/T]TCTGGGGAAAGAAGT	10529
rs375569591	snp	G/T	0.000232042	0.0107688	NEBL, LOC102725112	10	allele_origin=G(germline)/T(germline)	10:20845280	AGAAGGTTGGTGATG[G/T]ACTTTACATGTAAAA	10529
rs375589549	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20904792	ATCTGGAAAAACTTG[A/G]ATATGAGAGTGGATT	10529
rs375596212	snp	A/G			utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20783843	TATCACTTTAATCAC[A/G]ACTGGCCATTTCAGT	10529
rs375629195	snp	A/G			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20856351	CAATATTGCATAGGA[A/G]TGGCACGCTTTCTTC	10529
rs375632428	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:20791163	GGTAAGATTTATTGA[C/G]CAAAGATCTAGAAGC	10529
rs375635703	snp	C/T	1.65119e-05	0.00287327	intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20814012	AGACTTGGTCTACCT[C/T]TCATCTGTTTATGGT	10529
rs375648906	snp	C/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20884221	TTTATGTTTCACTTA[C/T]AGATTTTTTTGGCAT	10529
rs375657791	snp	C/T	0.00358779	0.0422022	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20852941	GTGGCAACGGAAAGC[C/T]AGCGCTAGGACATGC	10529
rs375658524	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20998498	TCCACTCTTGCCAGG[A/G]CTCTCAACAATAGGC	10529
rs375675325	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20975247	TAAAAATAAGATCTT[A/C]AAAGTACTAGAAGTG	10529
rs375685379	snp	C/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20845804	CATGTCCCCATCATC[C/T]TTCTTCATCAGACTT	10529
rs375700855	snp	A/G/T	9.9424e-05	0.00705005	intron-variant	NEBL	GRCh38.p7	10:20831434	CCAGCTATGATTCAC[A/G/T]GCATTTATTTTAAAC	10529
rs375708746	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20843128	TGGGATTGTGAGAGT[A/G]GGACTCCCTTGATAA	10529
rs375714953	snp	A/G	4.94956e-05	0.00497447	synonymous-codon, nc-transcript-variant	NEBL	GRCh38.p7	10:20812836	TTTATAGGCAGCATC[A/G]CTGACCACCTGGGTG	10529
rs375720338	snp	C/G	0.0130921	0.0798413	intron-variant, nc-transcript-variant	NEBL	GRCh38.p7	10:20813810	TTAGAAATGCCCCTC[C/G]CTCAAAAGACAAGCC	10529
rs375728589	snp	C/T	9.93049e-05	0.00704575	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20852530	AGGGTAGGTACCGTA[C/T]GGGCAAGTGTGTACC	10529
rs375733969	in-del	-/AG			intron-variant	NEBL	GRCh38.p7	10:21078449	TCCTCTCCTAAATAG[-/AG]TCGTGTATGTTGTCT	10529
rs375734344	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20804033	AAAATATTCATTTGG[C/T]CATTTTATTCCCTCT	10529
rs375737068	in-del	-/CAGAAAGAAGGAAAGA			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20882186	AGAAAGAAGGAAAGA[-/CAGAAAGAAGGAAAGA]AAGAAGGAAGTAAAG	10529
rs375746184	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21025496	AATTTTTTTTCTCTG[C/T]GAGATTCAGTTGTTA	10529
rs375750984	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:20827263	GGGTGGGAGAGCACG[C/G]TAGGAGAGATGTTTT	10529
rs375770201	snp	C/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20852455	GCAACTGTACTTTCT[C/T]AGTTAAGACGCACGG	10529
rs375771045	snp	C/T	6.64165e-05	0.00576228	intron-variant, synonymous-codon, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20859719	ACAACTTACATTGCT[C/T]GCCAGTGTAGCAGCA	10529
rs375771716	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21018301	TTTGATTGCTTGATT[C/T]AGTTCTATGTCCAGT	10529
rs375782791	snp	C/T	4.97006e-05	0.00498476	intron-variant, downstream-variant-500B	NEBL	GRCh38.p7	10:20817559	CACACGTGGACAATG[C/T]ATTTGATAGTGTAAG	10529
rs375814138	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20788888	TATTAGACTCTGGAA[A/G]CCTTGTCCATTGATT	10529
rs375814395	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21084771	TCTCCCTCCTGCTCC[A/G]TTGCCAGCAACATTC	10529
rs375816280	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21067431	CCAACGATTGTCATG[A/G]AATTGGATTATAAGC	10529
rs375823144	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21009891	TTTTAAGCACACATA[C/T]ATGTACTTCATGAGA	10529
rs375857274	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20943383	TTCATAGGTGGGAAC[C/T]GAACAATGAGAACAC	10529
rs375881815	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21117778	AAATATCAACTTTAG[A/C]GAATCAGTTGAGTAT	10529
rs375889092	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21109607	ATCTTTGGTAGAATT[C/T]GGCTGTGAATCCATC	10529
rs375893063	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20992922	AGCTGGGACTACAGG[C/T]GCCCGCCACCACACC	10529
rs375895800	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20825469	TGAGACCAGCCTGGC[C/T]GACATGGTGAAACCC	10529
rs375901649	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20955002	TATCCTAAAGGCAGC[A/G]GAGAGACTTAACAGA	10529
rs375902057	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20827058	CCACTTATTTGTTAA[A/C]CCTCTCCCATGTGTC	10529
rs375913174	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20816922	GTGGGAAGTGGAAAG[C/T]GGGGCTCGGAGGAAG	10529
rs375916508	snp	A/C/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20833749	CGACAGAGCGAGACT[A/C/G]CGTCTCAAAAAAAAA	10529
rs375919201	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21057874	ATTCATAACTTAACA[C/T]GACATGAAAAGGATA	10529
rs375941605	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20791789	AAAGGAAGAAATGTA[A/C]CCACAAGAAACGTTG	10529
rs375942267	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21151633	GGTTTACAGGCCTTG[C/T]AGGGTCCCCACCGTC	10529
rs375947675	snp	A/G			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21135984	GCCTGGATTGATTAA[A/G]CACATTTCTCAAAGA	10529
rs375950119	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20914437	CTCTATGTTTCCTAT[A/C]AATCCCTTTTCCCTT	10529
rs375959480	snp	C/T	0.0318195	0.122054	intron-variant	NEBL	GRCh38.p7	10:21069956	ATCATGTACTTACAG[C/T]GGCTTAGGGACTGCG	10529
rs375964583	snp	A/G	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20794826	AACATCCTTAGTCTC[A/G]GGCAATTTGGGATGT	10529
rs375968462	snp	A/C	1.94218e-05	0.00311617	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20852654	TTATATTCTCGCTAA[A/C]ATACAGAATGGGGAA	10529
rs375982678	snp	A/G	6.59696e-05	0.00574286	utr-variant-3-prime, synonymous-codon, nc-transcript-variant	NEBL	GRCh38.p7	10:20785861	GACGATGTAGTCGCC[A/G]TCTCTAAAGGAGACC	10529
rs375985605	snp	A/C	1.88824e-05	0.00307259	intron-variant	NEBL	GRCh38.p7	10:20840716	AAACATATTCATCTA[A/C]GGTGTTAAATAAACA	10529
rs375995750	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:20902407	CAAAGACACTGTCTC[A/T]AAAAAAAAAAAATTT	10529
rs375997275	in-del	-/ACACACAC			intron-variant	NEBL	GRCh38.p7	10:20963004	AAGCTTGAAAGAAAA[-/ACACACAC]ACACACACACACACA	10529
rs376013626	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:21047293	GAGACATTCCTTTGT[C/G]AAAATGTCTGCCAAT	10529
rs376023264	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20860282	CATCATTTCCTATAC[G/T]TCATTTGCTCAAAAA	10529
rs376032752	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21164700	CTACAATGACTTAAA[A/G]GATACCAAAATGCAT	10529
rs376037872	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20808307	GAAGTAAGACGGGGG[A/G]AAAATAACATGCAAA	10529
rs376044070	snp	A/G	0.000116373	0.00762711	intron-variant	NEBL	GRCh38.p7	10:20809769	CACTTTTGGGACAAA[A/G]CCACATAAATGGGAT	10529
rs376052158	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:21116228	CTTAAACAACAGATA[-/A]TTTATTTCTTACCAT	10529
rs376063594	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20890741	CAGAATTGTTATGCC[A/G]GGGGAAGACCCGGGT	10529
rs376069735	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21032964	TATCGGCTATTGAAA[C/T]ATGTCACCTAGATTT	10529
rs376070789	snp	A/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20871741	TCATTTCAGGTAGGT[A/T]TTATGCACACAGGTA	10529
rs376079598	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:21058916	TACTAATTGTGTAAA[C/G]TTGAGCAGGTCAAAG	10529
rs376080967	snp	A/G	3.36581e-05	0.00410219	intron-variant, upstream-variant-2KB	NEBL, LOC102725112	GRCh38.p7	10:20845371	CTTTGTAAACTTTCT[A/G]TTAAATAAGACCACA	10529
rs376096233	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20937095	ATGACACAGGCTCAG[C/T]TTTCTCCTGCCCTAC	10529
rs376097780	snp	C/T	0.000153988	0.00877328	intron-variant, nc-transcript-variant	NEBL	GRCh38.p7	10:20813920	AGCATGTTTTAAGAA[C/T]GATCTGGTTGGACCC	10529
rs376098924	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:20922453	CCTCCCTCCTATACC[-/A]AAAAAGCAAACTCAT	10529
rs376124710	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20937797	AGGAGATCATATCCT[A/G]TGCCTGGCTCAGAGG	10529
rs376137479	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20807307	CTCCAGCCTGGGCAA[C/T]AGAGCAAGACTCTAT	10529
rs376137965	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20911224	GCAGTAAGTCCTTTA[C/T]ACATCTTATCTCATA	10529
rs376140041	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20918715	AACTATACAGGCGTG[A/G]TGGCGGGCGCCTATA	10529
rs376140345	in-del	-/AAAT	0.0142736	0.0832652	intron-variant	NEBL	GRCh38.p7	10:21049009	GAGAGACTCCAACTC[-/AAAT]AAATAAATAAATAAA	10529
rs376147376	in-del	-/TTTTTTT			intron-variant	NEBL	GRCh38.p7	10:21039061	TTTTTGATGGGGCTG[-/TTTTTTT]TTTTTTTTTTTTTTT	10529
rs376172657	in-del	-/GGCC			intron-variant	NEBL	GRCh38.p7	10:20903902	TAAAATCTACGGATT[-/GGCC]GGGAACAATTACACT	10529
rs376202998	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20929786	ACAGATGAAAAGTTA[C/T]GAAATGAGTACAGGG	10529
rs376204920	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21164949	GCAGGGCACATTGCA[C/G]TGGATGCTAACTAGA	10529
rs376240154	in-del	-/A	0.0912534	0.193131	intron-variant	NEBL	GRCh38.p7	10:21074074	GTGAGACTCCGTCTC[-/A]AAAAAAAAAAGAAAT	10529
rs376243175	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20821871	TCTTGAATCCTGGAA[A/C]AAGCCTTGGATCTTG	10529
rs376255795	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20962200	GTAGAAAAAGAAAGC[C/T]AAATCTTCTTCTCCT	10529
rs376257731	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20951685	CCTGCCTCTAAAACT[C/T]CATTGACATTATAAT	10529
rs376261820	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21152148	GTCTTCCAGGGCCTG[C/T]GAGGAATGCAGGCGG	10529
rs376290488	in-del	-/A			intron-variant, upstream-variant-2KB	NEBL, LOC102725112	GRCh38.p7	10:20845405	TTTTAAAGTTAGCAA[-/A]TATCAGTGACCATTG	10529
rs376292606	multinucleotide-polymorphism	CTC/TTT			intron-variant	NEBL	GRCh38.p7	10:20930475	CAGCCAAGGTAGTCT[CTC/TTT]TGAAAATGCAAATTA	10529
rs376309590	in-del	-/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20848002	CTGCACATTTTTTTT[-/T]CTAAATGGGAAATGG	10529
rs376328405	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:21090624	ATTAGTCACACTTAA[C/G]ACTTTTATTTTGGTA	10529
rs376350061	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20995217	CAGCACCCCCCAGTC[C/T]CTGAGAACAGGAGCC	10529
rs376357456	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21169073	AAAAAAAAAAATATA[A/T]ATATATATATATATA	10529
rs376382402	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20783339	TTGTTCAGTTTTAGT[C/T]TTCATTGTAAAACAA	10529
rs376396934	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21022213	CAAAGAACATCCTCC[C/T]TGTTTGCTTCTTTCT	10529
rs376405982	snp	G/T	4.0256e-05	0.00448625	intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20828632	TTCATCTTTATACTT[G/T]CTCTAAAAACATAAA	10529
rs376406827	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:20825967	GGCAGAAGCGTGTCT[C/G]ATAAAAAGCTTAGAG	10529
rs376409987	snp	A/G	0.0023933	0.0345097	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20869435	GAGAGATTATATGGG[A/G]CCATATGACTGATAA	10529
rs376429595	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21050212	ATTAGATACGTGCTG[A/C]TAAATTCTTACTTTC	10529
rs376435899	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21018975	GAGGTTGCAGTGAGC[C/G]GAGACGGCACCACTG	10529
rs376436100	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20988651	ACATACTGTGTCACC[C/T]AGATCCCTGTTTTTC	10529
rs376445700	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21096330	ATGGAATATAAACCA[A/T]AATACAATTTGCATA	10529
rs376450435	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21048195	TCTCCCCTCGCACGC[G/T]GTCCTCAAAGAGTTG	10529
rs376456870	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21048564	TGCAGTCTTAGAGTC[C/T]TTCCAAGAAACAGAA	10529
rs376458172	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20801315	CCTCCTGGGTTCAAG[C/T]GATTCTCATGCCTCA	10529
rs376466999	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20887766	TCAAATATTCTCTAC[C/T]TAGGGATCATATATC	10529
rs376472700	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20816910	GGAGTCATGATTGTG[A/G]GAAGTGGAAAGTGGG	10529
rs376487908	snp	C/T	0.000106159	0.00728479	intron-variant	NEBL	GRCh38.p7	10:20823324	TTTATAAGAATATAA[C/T]GTTAACTTTATTCTA	10529
rs376496893	snp	A/C			intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20960160	GTTTAGTTCTTTTTG[A/C]AATAAAATTCAGTGA	10529
rs376499102	snp	C/T	0.000153988	0.00877328	intron-variant, missense, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20852640	CCTCAAAGAGCTTTT[C/T]ATATTCTCGCTAAAA	10529
rs376501949	in-del	-/T			intron-variant	NEBL	GRCh38.p7	10:21091520	CTTTATCCAATTAGC[-/T]ATCAGTACCTCAAGT	10529
rs376511347	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20934063	AAGGCCCCATTTTAC[A/C]CTTCAACTTTTTGTG	10529
rs376512621	snp	A/G	0.000117348	0.00765899	intron-variant, upstream-variant-2KB	NEBL, LOC102725112	GRCh38.p7	10:20845226	TCTTTACTTTTCTTC[A/G]TAATATTTAATAATA	10529
rs376512794	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:20985618	TGCTACTCATTTCAG[G/T]CAGTCAGAAACATCT	10529
rs376531123	snp	C/T	0.00914312	0.0669923	intron-variant	NEBL	GRCh38.p7	10:20941273	CCTGGGATGCAAGGC[C/T]GGTTCAACATACGCA	10529
rs376535051	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21074720	CCTGACCTCATGATC[C/T]GCCTGCCTCGGCCTC	10529
rs376548903	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21072422	GTTGTAGGTGGACAT[G/T]TCTGTTGGGTCCCCT	10529
rs376549765	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20943842	CCTCAAGCAAGCATC[C/T]TCATAAGCTGGCAAA	10529
rs376561730	snp	A/G			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20875844	ACTGATTCTTGGTGA[A/G]AAGAAACTAGACAGG	10529
rs376563604	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21018345	GAATTACCTGATGAA[A/C]CCTAACTTGACGAGA	10529
rs376570509	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20993815	GGAAGGAAAACACTT[C/T]GACAATTACAGAGGC	10529
rs376579656	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20901761	GGTTTTTGTTTTGAT[A/G]ACCGTCTTCCGGAAG	10529
rs376596119	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:20910829	TGTTTTTCGTTTTTG[G/T]TTTTTTTTTTTTGGC	10529
rs376599033	in-del	-/AGAAACAAA			intron-variant	NEBL	GRCh38.p7	10:20818385	ACATCTACCAACCAG[-/AGAAACAAA]AGAAACAAACAGTGC	10529
rs376602722	snp	C/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20867691	AATCCACCTGGAATT[C/T]ATTTTTGTATATGGT	10529
rs376610720	snp	C/G	0.0103295	0.0711199	intron-variant	NEBL	GRCh38.p7	10:20942341	CAAGAAATGGGGAAA[C/G]GATTCCCTATTTAAT	10529
rs376613955	in-del	-/GA			intron-variant	NEBL	GRCh38.p7	10:21038043	AGAGAGAGAGAGAGA[-/GA]AAAGTTTGCCTCTAA	10529
rs376641589	snp	A/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20864293	GCACCAATCCCTTCA[A/T]CTTCGCATAGGAGAT	10529
rs376650503	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21031808	CTCACTTCTTCCAGG[A/G]CAGAGTATACACATA	10529
rs376657963	snp	A/C	0.00517822	0.0506191	intron-variant	NEBL	GRCh38.p7	10:21036043	TGGCGCGCACCTGTA[A/C]TCCCAGCTACTCAGG	10529
rs376662936	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:20822702	TATATAGAGACTATA[G/T]ATACGTATATATGTC	10529
rs376662989	snp	A/T	0.00795532	0.062565	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20863720	TAGTGGATCAAAGGC[A/T]TATGAGCCCTGTCTC	10529
rs376666481	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21059899	CCAAACTGGGGATCC[G/T]TCTTTGGGAAGGTTT	10529
rs376667875	snp	C/T	0.00517822	0.0506191	intron-variant	NEBL	GRCh38.p7	10:20799397	CTGGACTCTAGTGAT[C/T]CACCCACCTCCGCTT	10529
rs376677907	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20965742	CAGGACAGACGCGAG[A/G]AGCCCAGGTAGAGTC	10529
rs376679491	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20794122	AATTTGGAGGTTAGC[A/G]TGCAACATTCCTGGG	10529
rs376680302	snp	G/T	4.94809e-05	0.00497373	intron-variant, synonymous-codon, nc-transcript-variant	NEBL	GRCh38.p7	10:20889905	ACTGTCAGTCACAAA[G/T]GTACACTTATCCTTG	10529
rs376686844	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21094013	TCTGTGGTTTGACAC[A/C]TTAAGCATCACTACT	10529
rs376689463	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20924286	ATTGAGAAGCCCTGT[A/G]TCTTCTGAGACCCTG	10529
rs376690666	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21061717	AGTTCTTCCTTTAAA[G/T]GATGTTTTTATCCCT	10529
rs376692428	snp	A/G	0.000153988	0.00877328	intron-variant, synonymous-codon, nc-transcript-variant	NEBL	GRCh38.p7	10:20809882	GGAGCCAGGATCTGT[A/G]CGCCAAACTTTGAGG	10529
rs376692887	snp	A/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20856043	TGAGCAAATGTATAC[A/T]GCTTTATACAATGTA	10529
rs376696947	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21028442	GCAAGCAAATAAAAT[A/G]TAAATGTGCACACAC	10529
rs376697026	snp	C/G/T	8.38503e-05	0.00647448	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20961831	ATCACGAATCCCACT[C/G/T]GGGATAGGCTGGGCC	10529
rs376742884	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:21151752	CCTTGCCTATACCAG[C/G]TTTTGCTCCAATGTG	10529
rs376754098	snp	C/T	3.41676e-05	0.00413311	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20850534	AAAGCATATACAAAT[C/T]GAAAGTCCTTATACA	10529
rs376772493	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21104665	TAGACAATCATGTGG[C/T]CTGTGAATGAAGGTA	10529
rs376773307	snp	G/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20953215	TCAGGGCTTCCTTGT[G/T]ACTTCATTTAACCTT	10529
rs376780113	snp	C/T	1.77568e-05	0.00297961	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21126166	CTTCAAGCCTGGTAC[C/T]CCCCATAGAAAGGAA	10529
rs376795002	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20955953	AATTCTTTTATTACC[A/G]GGGCTCTTCTCAAAC	10529
rs376799953	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21101058	GGAGGTTATTTCCTT[C/T]ATTCACAGGCCTGAA	10529
rs376800198	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21121839	ACCAAAATGAAGTGA[C/T]AGAAAATGCAAATTT	10529
rs376828973	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21057348	ATCTCAGGTAAAACA[A/C]AAAAGCAAGATGTGG	10529
rs376842299	snp	C/G	0.000148853	0.00862578	NEBL, LOC102725112	10	allele_origin=G(germline)/C(germline)	10:20852537	GTACCGTACGGGCAA[C/G]TGTGTACCTGACTTT	10529
rs376845093	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:21053747	ATTTAAGAAGTATGC[C/G]TAGGGCTGGGCATGG	10529
rs376852606	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:20933206	GCATCAGTCCCTCCT[C/G]ACCCAAAAACTAATT	10529
rs376853655	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20971765	ACTATAGGCGCCCAC[C/T]ACCACACCCAGCTAA	10529
rs376862957	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21073918	TCTCTACTAAAAATA[A/C]AAAAAAATTAGCCGG	10529
rs376868110	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20990594	GTCTGTTGTTTAAGC[C/T]ACCCAGTCTATGGTA	10529
rs376881351	snp	C/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20852330	TTATTTTACAAAATG[C/T]CTTTAGATTGAAATA	10529
rs376881743	snp	A/C/T	0.00597247	0.0543191	intron-variant	NEBL	GRCh38.p7	10:21119210	CCTGAATTTAACAGC[A/C/T]CAACATTTTTCTCCA	10529
rs376891298	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:21026572	CTCCATCTTCTCCCT[C/G]CTGAGCACTTAAGTC	10529
rs376899604	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20912959	TAGACACAGGGTCTC[A/G]CTATGTTGCCCAGTC	10529
rs376906412	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20818001	AAAGAAACGCCAGAA[C/T]GAAGTCATTACAAGA	10529
rs376920221	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21072005	TGTGTTTTAGTAGAG[A/C]TGGGGTTTCACCATG	10529
rs376934491	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20994663	AGCCTGCTATTCACT[A/G]GAAGCTTTACTGATA	10529
rs376942792	snp	C/G	0.00478085	0.0486577	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20898032	TTCTGCAGTTCTACT[C/G]ATCATGTCAATTTTT	10529
rs376946877	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20978335	GATCAATAATATCCC[A/G]AAGAATAGAGAGCTT	10529
rs376955202	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20867190	TTTAAATTTTTTAAA[A/C]CCTCTTTTTGGATTG	10529
rs376960948	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21030954	CCATTAGGACACACC[A/G]GTGTGCACTGATGAC	10529
rs376969226	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20902231	ACACTGTGAAACCCC[A/G]TCTCTACTAAACAAA	10529
rs376971303	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20805416	TCACTTGTGTTTATG[C/T]TATACAACTTATTGG	10529
rs376975373	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20918333	ACTGCACTCCAGCCT[A/G]GGTAACAGAGCAAGA	10529
rs376984939	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21097002	TAAAAAAAAAAGGTA[A/G]TATTTCCTGGCTTAT	10529
rs376996370	snp	A/C	0.000118849	0.0077078	intron-variant	NEBL	GRCh38.p7	10:20889962	GATCTAAAAAAGAGA[A/C]TGATTTACATAAGAA	10529
rs377003645	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:21106560	ATATCTGTTTTGGTA[C/G]CAGTACCAGCCTGTT	10529
rs377011568	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20948735	TATTACAACCTGCAG[A/G]ATTCTTAATATTCTC	10529
rs377012262	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20935817	AATAATCTAAGAAGA[A/G]TTTTTTTCACCTTCA	10529
rs377015213	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20967361	GGCTGGGCATGGTGG[C/T]TCACGCCTGTGATCC	10529
rs377041157	snp	G/T	1.65693e-05	0.00287826	missense, intron-variant, utr-variant-3-prime	C10orf113, NEBL	GRCh38.p7	10:21125852	TTTTCAGCACCTTCT[G/T]AGATACGTTGAACTT	10529
rs377042319	in-del	-/AT	0.00438332	0.0466095	intron-variant	NEBL	GRCh38.p7	10:21030665	AAGTAGGTGTGGTGA[-/AT]GTCCCAAAAGACCAC	10529
rs377050977	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:20803492	ATTTTAACTACATTT[G/T]GTTTTTAAAAGTAAA	10529
rs377065610	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20965738	TGTGCAGGACAGACG[C/T]GAGAAGCCCAGGTAG	10529
rs377073927	snp	A/G	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21027413	CATCACCGCAGCCTC[A/G]ACCTCCTGGACTCAG	10529
rs377078010	snp	A/G	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:20944332	GTGAACCTGGGAGGC[A/G]GAGGGTGCACTGAGC	10529
rs377088871	snp	C/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20941826	CAAATCATGAGTGAA[C/G]TCCCATTCACAATTG	10529
rs377096872	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20973783	CCAAAGTCTGGAGTG[A/C]ATCTTTCTCTCTAGT	10529
rs377105922	in-del	-/CT			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20875221	ATAATCCTCCCACTT[-/CT]GTTTCATAAGAGCCA	10529
rs377112923	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20894223	ACCTGTAATCCCAGC[A/C]CTCTGGGAGAACGAT	10529
rs377122105	snp	C/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20861734	TGCAAACTCTGAGGT[C/T]TCCAGCATAATTACA	10529
rs377153614	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21118436	ACGCATACTTAAAAA[A/G]AAACCTAAATTGAAA	10529
rs377155142	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21058290	CCAAGGAGAGCATAG[A/G]TATAATCCATTCTTG	10529
rs377156789	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21099026	CGGTCCTATCTACTC[A/G]GAAGGCTAAGGCGGT	10529
rs377170675	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:20904050	ATAGCAAGAGAACAA[C/G]TAGTAATAAAATAGA	10529
rs377179222	snp	C/T	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20977537	GAGAGGCATCACAGA[C/T]AGGCGAGCTGGCCTG	10529
rs377186390	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21157794	GACCTATTTGGAGAT[A/G]GGGTCTTTGCTGAGG	10529
rs377222699	snp	A/G/T			intron-variant, downstream-variant-500B	NEBL, LOC102725112	GRCh38.p7	10:20885312	ATAAAATCGATGTAC[A/G/T]TAAATCTAAAGAAAT	10529
rs377226276	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:20908062	CACTGACCTATACCA[G/T]GTACCGAGAAAAGGT	10529
rs377230358	snp	A/G/T	0.000181319	0.00951998	NEBL, LOC102725112	10	allele_origin=G(germline)/T(germline)	10:20880784	AATCATGAGAAATGC[A/G/T]CTTCCTTACATTACT	10529
rs377236750	snp	A/G	6.76293e-05	0.00581464	intron-variant	NEBL	GRCh38.p7	10:20787193	GGAACGTATCAAATG[A/G]ACACTTACTAGATTT	10529
rs377237960	snp	G/T	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20912313	TGCATTAGCTGGGTG[G/T]GGTGGTGTGTGCCTG	10529
rs377240146	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21057188	AAATCTTATTTAAAA[C/T]AACAGAGAGGTTATA	10529
rs377246948	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21094226	GCCAGGTGTAGGCCG[G/T]AGACGGTGGCTCACG	10529
rs377247074	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21046556	TTCTGCTTTAAAAAA[A/T]TTGGATTCTTTAGCG	10529
rs377247460	snp	A/G			upstream-variant-2KB, intron-variant	C10orf113, NEBL	GRCh38.p7	10:21147854	ACTGGCCTTCCTGTC[A/G]CCAACCAAATTCAAT	10529
rs377253471	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21124797	CATTGTTACCAAAAA[C/T]ACACGTTTTAAAAAT	10529
rs377255257	snp	C/T	0.00755907	0.0610114	intron-variant	NEBL	GRCh38.p7	10:21116819	GGACTACAGGTGTGC[C/T]GCACCAATCCCAGCA	10529
rs377258024	snp	A/G	0.000569422	0.0168638	intron-variant	NEBL	GRCh38.p7	10:21069919	TTTTCCCCTGATAGC[A/G]CAAGTCATGTAAATA	10529
rs377262453	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20979497	ATTTATGTTTTACTC[A/G]TATAATTCTCAGAAG	10529
rs377285662	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21019943	GGACAATTCAAGACC[G/T]GGAACAGTACAGATG	10529
rs377289818	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20914933	CACAATCTTGACTCA[C/T]GCAATTCTCCTACCT	10529
rs377307039	snp	A/G			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20849476	TGATCAGGCCATAGC[A/G]CTCTGCCTCATGAAT	10529
rs377315695	snp	C/T	1.65523e-05	0.00287678	intron-variant, splice-donor-variant	NEBL	GRCh38.p7	10:20831195	TTCATTCATGACCAA[C/T]CTGGCTATAGATTTC	10529
rs377317796	snp	C/G/T	0.000133347	0.00816447	intron-variant	NEBL	GRCh38.p7	10:20808665	CTCGCCTTTTCTATA[C/G/T]TGGAGGGAAAATATT	10529
rs377350784	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21078355	TTCAAATTATTACAA[C/T]GAACACTTTTATGAT	10529
rs377359197	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:20947973	ACAAAAAAATATGTT[A/T]ACACTAACAAAAGGT	10529
rs377370120	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20993327	TGATTTACTGGTAAG[A/G]TGAGAACAAGGATCT	10529
rs377383343	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20984100	TTGCAGGCAAACATC[C/T]AAAAATCCAACAGAA	10529
rs377385301	snp	G/T	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21133544	ATCAGATCCTCCCCA[G/T]CTTAAACTAAGAAGA	10529
rs377393914	snp	G/T			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21133152	TTGTATGTGTGTGAG[G/T]TGGGAGTCCAATTTT	10529
rs377398485	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20905126	GGGTTGTAGAGCATA[C/T]TGCAAACAACCATTA	10529
rs377399053	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20924841	AGTTAACCATAATCC[A/G]GCTGGCGCTATAAAA	10529
rs377408048	snp	G/T	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:20818400	ACAGTGCTGACCTCA[G/T]GGGTTTACATAGAAC	10529
rs377410767	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21085860	ATTTACATCTCACTC[A/G]GCAGGGCAGGCAAGT	10529
rs377414261	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20833279	GGCTAAAGAAAGTCA[C/T]ATGGTCAAGCCCAGA	10529
rs377432531	in-del	-/T			intron-variant	NEBL	GRCh38.p7	10:20913601	AGTACAAAAACCAAG[-/T]GTACGAAATATCGTA	10529
rs377436400	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:21152584	GTCCAAGAAAAAAGA[-/A]AAAAAAAAAAATCCA	10529
rs377465213	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21088377	TTGTGGTCCCAGTTA[C/T]GCAGGAGGCTGAGGC	10529
rs377485549	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21168016	GCAAAATGGGTATTA[C/T]GCCCAATCTTACATC	10529
rs377490414	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21028245	CATCTCAAAAAAAAA[A/G]AAAAAAAAAAAGAAG	10529
rs377492976	snp	A/G	0.000230646	0.0107364	NEBL	10	allele_origin=G(germline)/A(germline)	10:20961724	AGCTCAGGAGTGTCC[A/G]TGACGATGCTGAAGC	10529
rs377494722	snp	A/C/G	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21142876	CATCCTCCTGCCCCC[A/C/G]ACCCCCAACATCTGT	10529
rs377505414	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21120879	TGGTTAATCTGGTTC[A/C]AAGGAATTATTCCAT	10529
rs377512096	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20798336	AGTCAGGAACCAATC[A/C]CCACAACCTACACGC	10529
rs377529626	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20968173	GTAGGAAAAATTGCA[C/T]TGAGAGAGTGTAAAA	10529
rs377541688	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20985051	CAGGAAAATAAGCTC[A/G]GGGCACTCACTGATT	10529
rs377543836	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20975015	AATTCCATGGTGTTA[C/T]AGGTACAATTATATT	10529
rs377554473	snp	C/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20999148	CTGTACAGAAACCCA[C/G]AGGTGTGTGGGGGGA	10529
rs377565559	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20812580	AAGACTTGAGATGAT[A/G]CCAGGTGAATGCCAG	10529
rs377568591	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21055910	ACATTAAAATCAGCC[A/G]GAGTATCTTGGCTCT	10529
rs377569493	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21049933	TGGTCTCTCCAGAAT[A/G]CCTCATTGATGAGGA	10529
rs377575230	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:20938581	ACAACGGAACAAAGC[G/T]GGATGGAGAATGACT	10529
rs377575441	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21097839	CATTGGACTTTTTTA[C/T]GGATGTAATAGTCAC	10529
rs377588301	snp	A/T	1.6492e-05	0.00287154	intron-variant	NEBL	GRCh38.p7	10:20835469	TACGATTTGTTAGGT[A/T]CCAAAATATGAGTCT	10529
rs377597431	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21085836	AAGAGGCAAAAATAT[A/G]CACTTCTCATTTACA	10529
rs377618156	snp	C/T	1.64939e-05	0.0028717	missense, intron-variant, utr-variant-3-prime	C10orf113, NEBL	GRCh38.p7	10:21126016	CTGAAGCTGACTCTC[C/T]GCAGCCACCTGGCAA	10529
rs377624818	snp	A/C	3.31417e-05	0.00407059	intron-variant, synonymous-codon, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20859734	CGCCAGTGTAGCAGC[A/C]AGCTGATTCTGCCTA	10529
rs377626798	snp	A/T	0.000595829	0.0172499	intron-variant, downstream-variant-500B	NEBL	GRCh38.p7	10:20817567	GACAATGCATTTGAT[A/T]GTGTAAGAAAAAAGT	10529
rs377643193	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20996191	GTTAATGTGCCACTA[A/C]GATGTGATACGCTTT	10529
rs377648518	snp	A/C	0.000335542	0.0129483	NEBL, NEBL-AS1	10	allele_origin=A(germline)/C(germline)	10:21173750	TCCAGGCTGGCCCGG[A/C]GCCCCCTCGCTCACC	10529
rs377656601	snp	C/T	6.61529e-05	0.00575083	intron-variant	NEBL	GRCh38.p7	10:20785958	TTATACGATGAATGC[C/T]GAAATAGCTACAGCC	10529
rs377658800	snp	A/G			upstream-variant-2KB, intron-variant	NEBL, NEBL-AS1	GRCh38.p7	10:21175034	CTCGTAGTCCAAACC[A/G]GAAGAGCCAGAAAAT	10529
rs377675186	snp	A/G/T			intron-variant	NEBL	GRCh38.p7	10:21022420	CACGCTAGCACTTGC[A/G/T]AAATAAAGATTAAAT	10529
rs377676673	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20971893	GCTGGGATTACAGGC[A/G]TGAGCCACCACGCCC	10529
rs377677719	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:21052185	AAGGAAATGCAAGTT[C/G]CAATGAGCTGTCACC	10529
rs377677765	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20850213	GAGAGAAGCTAAGGA[C/G]CAGATAAACTCAATG	10529
rs377683419	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20832587	TTTTCTATATGTATA[C/T]TATTCTTCAAAGAAA	10529
rs377686207	snp	C/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20876932	GGTACAAAAAGATTT[C/T]GATTGGCTGTTTTTA	10529
rs377694675	in-del	-/TA			intron-variant	NEBL	GRCh38.p7	10:21022802	TGGACTGTCAAGAGA[-/TA]ATTTCTCACACACAG	10529
rs377702958	snp	C/T	4.95626e-05	0.00497784	intron-variant, synonymous-codon, utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20815625	AAGAAAACCACTTGC[C/T]GAGCTAATATTTTCT	10529
rs377708087	snp	A/G			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20870951	GCCCATGTTTCACTG[A/G]TCAGCTCACTTCTTT	10529
rs377709797	snp	G/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21049983	CCAGGAAACCAAAGT[G/T]AACATGAAAGGTTAC	10529
rs377740554	snp	C/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20858906	AGTAGCCCCATTTTA[C/T]AGATAAGAAAACTGA	10529
rs377744847	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:21077332	TTTGCTGGCCGGGCG[C/G]AGTGGCTCACGCCTG	10529
rs377747725	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20906039	CTTCAGAATACTCTT[C/T]GTGTATGTGGACTTT	10529
rs377751546	snp	C/T			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21141041	GACATCAAATAAATA[C/T]AAAACAAGAGGTATT	10529
rs386370893	in-del	-/AA			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20860586	AAAAAAAAAAAAAAA[-/AA]ACCTAGCTATTCACA	10529
rs386370895	in-del	-/AT			intron-variant	NEBL	GRCh38.p7	10:20921797	GCACACACACACATA[-/AT]TGTATACACACATGC	10529
rs386370898	in-del	-/AAA			intron-variant	NEBL	GRCh38.p7	10:21044425	AAAAAAAAAAAAAAA[-/AAA]AAGCTCCTAACTGCA	10529
rs386370899	in-del	-/CAGT			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21132031	TAAAATGTATAATTC[-/CAGT]AGTTTTAGTATATTC	10529
rs386741733	multinucleotide-polymorphism	CC/TG			intron-variant	NEBL	GRCh38.p7	10:20806264	CCAAGCAGAGGCCCT[CC/TG]GAATTCCTGATCTCT	10529
rs386741734	multinucleotide-polymorphism	AA/GC			intron-variant	NEBL	GRCh38.p7	10:20810199	TCACACAACACAGGA[AA/GC]ACATGGGGCAGCTAT	10529
rs386741735	in-del	AA/T			intron-variant	NEBL	GRCh38.p7	10:20814749	ATAAGAGTGTTAAAA[AA/T]TGCATACAAGCTACT	10529
rs386741736	multinucleotide-polymorphism	CA/TG			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20852540	CCGTACGGGCAAGTG[CA/TG]TACCTGACTTTGGAG	10529
rs386741737	multinucleotide-polymorphism	GC/TT			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20865153	TGGAATGAATTTAAG[GC/TT]CAGAATCTCACAGAC	10529
rs386741738	multinucleotide-polymorphism	AC/GT			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20870795	GCATGTTAGACACAA[AC/GT]CAAAGTATGGTAAGT	10529
rs386741739	multinucleotide-polymorphism	CT/GA			intron-variant	NEBL	GRCh38.p7	10:20903459	GGAGACAATATGAAG[CT/GA]TTTTTAAAGAACTAA	10529
rs386741740	multinucleotide-polymorphism	AT/GC			intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20960512	AAAGAGCAAAAAACA[AT/GC]GTGTACTTTGCATCC	10529
rs386741741	multinucleotide-polymorphism	CTC/GTT			intron-variant	NEBL	GRCh38.p7	10:20977898	TAACTCAAGCCTAAC[CTC/GTT]CCTGCTCATCTCTAG	10529
rs386741742	in-del	ACG/CA			intron-variant	NEBL	GRCh38.p7	10:20978441	TAACCAAAAAAAAAA[ACG/CA]AGTTATTTGATTAAA	10529
rs386741743	multinucleotide-polymorphism	AGC/CTT			intron-variant	NEBL	GRCh38.p7	10:20978829	AAAAATAAAAGTTGG[AGC/CTT]CACTCGAGAGCAAGA	10529
rs386741744	multinucleotide-polymorphism	CAC/TAA			intron-variant	NEBL	GRCh38.p7	10:20983789	TCCAGGAAAATGCTA[CAC/TAA]ATGACATGTACAATA	10529
rs386741745	in-del	GTGTACA/TAGAC			intron-variant	NEBL	GRCh38.p7	10:20985129	AATAATAGACATAAA[GTGTACA/TAGAC]ATAAATGTAATGTAC	10529
rs386741746	multinucleotide-polymorphism	CA/TG			intron-variant	NEBL	GRCh38.p7	10:20989263	TACCTAGTTTAAAAA[CA/TG]TATTTAATCCAACTT	10529
rs386741747	multinucleotide-polymorphism	GG/TA			intron-variant	NEBL	GRCh38.p7	10:20996669	CACTAGTTCTCAGGG[GG/TA]CTAGACTGTAATGTG	10529
rs386741748	multinucleotide-polymorphism	CCT/TCC			intron-variant	NEBL	GRCh38.p7	10:21005348	AATTGGCCAGATTAG[CCT/TCC]CCAGCAGCCTGAATG	10529
rs386741749	multinucleotide-polymorphism	CA/GT			intron-variant	NEBL	GRCh38.p7	10:21017393	ATTGCTTCTAAAGAA[CA/GT]CGACATTTGAGCAAA	10529
rs386741750	multinucleotide-polymorphism	CC/TT			intron-variant	NEBL	GRCh38.p7	10:21027789	CATTTTACCCAATGA[CC/TT]AAGACCATAACTAAC	10529
rs386741751	multinucleotide-polymorphism	AA/TG			intron-variant	NEBL	GRCh38.p7	10:21032366	AAGGCATAATTATAA[AA/TG]ACTATAAGCCTGATA	10529
rs386741752	multinucleotide-polymorphism	CGCAGGCACCTGTTGCCAGACATCCTA/TGCAGGCACCTGTTGCCAGACATCCTG			intron-variant	NEBL	GRCh38.p7	10:21034468	TTCTCAGCACAGTAA[lengthTooLong]GAGCACAGGATAAGC	10529
rs386741753	in-del	ATCAAAAAACACTCCCCTAATGAAGAGTAGAAAGATAA/GTCAAAAAACACTCCCCTAATGAAGAGTAGAAAG			intron-variant	NEBL	GRCh38.p7	10:21037791	CAAGATAAATTGGAG[lengthTooLong]ATAGACAAAATGAGA	10529
rs386741755	multinucleotide-polymorphism	CCT/TCA			intron-variant	NEBL	GRCh38.p7	10:21057637	TCACGGCAACCTCTG[CCT/TCA]CCGAGGCTCGAGCAA	10529
rs386741756	multinucleotide-polymorphism	CGC/TGA			intron-variant	NEBL	GRCh38.p7	10:21088937	GCAGTTAATGAACCA[CGC/TGA]GAGGCAGGAAAGATT	10529
rs386741757	in-del	AAA/GC			intron-variant	NEBL	GRCh38.p7	10:21104553	CCAGTACATAGAAAT[AAA/GC]AAATGATTTTTATAT	10529
rs386741758	multinucleotide-polymorphism	ACC/GCT			intron-variant	NEBL	GRCh38.p7	10:21111158	AATATCATGAAAATG[ACC/GCT]ATATTTCCCAAGGTA	10529
rs386741759	multinucleotide-polymorphism	AC/GA			intron-variant	NEBL	GRCh38.p7	10:21122103	CGATCTCGGCTCACT[AC/GA]AACCTCCACCTCCCA	10529
rs386741760	multinucleotide-polymorphism	AAT/GGA			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21137962	GGAAGGGAAGGGAAG[AAT/GGA]ATGGAAAGGAAGAAA	10529
rs386741761	multinucleotide-polymorphism	CC/GG			intron-variant	NEBL	GRCh38.p7	10:21151859	ATCTCTTCCCCTGCT[CC/GG]ATTTTTCTCTATAGA	10529
rs386741762	multinucleotide-polymorphism	CGT/TGC			intron-variant	NEBL	GRCh38.p7	10:21159313	GGGTATGGCACACAT[CGT/TGC]TTATCTTAGAGTTTC	10529
rs386741763	multinucleotide-polymorphism	AAA/CAG			intron-variant	NEBL	GRCh38.p7	10:21163203	AGTCTGCTAGAAACC[AAA/CAG]TTTTTTTTCCTATAA	10529
rs386741764	in-del	C/TCCTCCTAGA			intron-variant	NEBL	GRCh38.p7	10:21163805	TAGTTCTCTTCTGGC[C/TCCTCCTAGA]ATTCAATAAGAATGA	10529
rs397517203	snp	A/G	0.00156372	0.027918	NEBL	10	allele_origin=G(germline)/A(germline)	10:20896991	AGACTTAAGCATGGA[A/G]TTGGCCAGAAAATGC	10529
rs397517204	snp	G/T	0.0036014	0.0422815	NEBL	10	allele_origin=G(germline)/T(germline)	10:20896943	TGTAAGTGGCTGGAG[G/T]AATTTTTGTCTTATT	10529
rs397517205	snp	A/G			intron-variant, missense, synonymous-codon, nc-transcript-variant	NEBL	GRCh38.p7	10:20815690	GGTCAGCTGGGAAGA[A/G]CTACCACTTTAAGTG	10529
rs397693165	in-del	-/A	0	0	intron-variant	NEBL	GRCh38.p7	10:20984136	CCTGAAAAAAAAAAA[-/A]GCTCCAAACTTCTAA	10529
rs397696495	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:21076120	CTATTACAAAAAAAA[-/A]CTGTATAGCAATTCC	10529
rs397698198	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:20843554	TTCTCCTTTAAAAAA[-/A]TTAACATAAATAGTG	10529
rs397706843	in-del	-/T	0	0	intron-variant	NEBL	GRCh38.p7	10:21064224	TTCATTTGAATTCAA[-/T]TTTTTTTGACGTTAA	10529
rs397712978	in-del	-/AT			intron-variant	NEBL	GRCh38.p7	10:20921798	CACACACACACATAT[-/AT]GTATACACACATGCA	10529
rs397717025	in-del	-/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20851991	GGAACTGACATCTTT[-/T]GCAACTATTTAAGCT	10529
rs397727487	in-del	-/T			intron-variant	NEBL	GRCh38.p7	10:20910841	TGTTTTTTTTTTTTT[-/T]GGCCAAAGGGGGATA	10529
rs397735663	in-del	-/C			intron-variant	NEBL	GRCh38.p7	10:21026337	ACACTGTACAGCCCC[-/C]TCCCTGACAGACTTA	10529
rs397739040	in-del	-/A	0	0	intron-variant	NEBL	GRCh38.p7	10:21037450	TTGCAAAGAAAAAAA[-/A]TGGGAATCAGAAATA	10529
rs397741463	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:20787591	AAAACATAAACAAAA[-/A]TTTTTCATACTCCCT	10529
rs397744657	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:21024082	GAAAAAAAAAAAAAA[-/A]CATTGAAAAGCTTCT	10529
rs397745327	in-del	-/AAC			intron-variant	NEBL	GRCh38.p7	10:20904048	TCATAGCAAGAGAAC[-/AAC]TAGTAATAAAATAGA	10529
rs397748070	in-del	-/A	0	0	intron-variant	NEBL	GRCh38.p7	10:21067988	CTCAAAGAAAAAAAA[-/A]TGTAATATACTTCCC	10529
rs397754645	in-del	-/A	0	0	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20868848	CCAAAAAAAAAAAAA[-/A]TAACAGACCTTCATC	10529
rs397765405	in-del	-/A	0.42	0.183303	intron-variant	NEBL	GRCh38.p7	10:21089852	TGGGTTTTCCAAAAA[-/A]CATGTCCATAGTTCC	10529
rs397765462	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:21077230	TTTCTTCAAAAAAAA[-/A]TAAAAAATCAAAGGA	10529
rs397766146	in-del	-/TT			intron-variant	NEBL	GRCh38.p7	10:20795126	AATTCAGAAAAGTGT[-/TT]AAGAGTACTATGGCA	10529
rs397795704	in-del	-/A			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21130123	TCAAAACAGGGTAGA[-/A]CTTCAAAACAGGGAA	10529
rs397801923	in-del	-/T			intron-variant	NEBL	GRCh38.p7	10:21103742	CTCTGGCTCCCTAGT[-/T]CATGACATGCGATTA	10529
rs397808821	in-del	-/A	0	0	intron-variant	NEBL	GRCh38.p7	10:21027311	ATCTTTAAAAAAAAA[-/A]CAACAACTTTTTTTG	10529
rs397816422	in-del	-/AC			intron-variant	NEBL	GRCh38.p7	10:21046024	CACACACACACACAC[-/AC]GTGTGTGCACTGGAA	10529
rs397819593	in-del	-/G			intron-variant	NEBL	GRCh38.p7	10:21162357	ATCAAATCTGAGGGG[-/G]GTCGTGGGAACTCTC	10529
rs397819860	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:20894769	AAAAAAAAAAAAAAA[-/A]TACAAAAAAATTAGC	10529
rs397821662	in-del	-/ACAC	0	0	intron-variant	NEBL	GRCh38.p7	10:20963044	CACACACACACACAC[-/ACAC]GGAAATCTAGATACT	10529
rs397824607	in-del	-/T	0	0	intron-variant	NEBL	GRCh38.p7	10:20886541	CTTAAAAAAAGAAAT[-/T]CTGGGGAAAGAAGTA	10529
rs397829256	in-del	-/T	0	0	intron-variant	NEBL	GRCh38.p7	10:20926407	ATGTGAAATTTTGCT[-/T]CTTTTATGATCTCAT	10529
rs397844773	in-del	-/G			intron-variant	NEBL	GRCh38.p7	10:21162358	TCAAATCTGAGGGGG[-/G]TCGTGGGAACTCTCA	10529
rs397844881	in-del	-/C			intron-variant	NEBL	GRCh38.p7	10:21160984	ATTTTTATAAACTAC[-/C]TTTGTAGACATTATT	10529
rs397845127	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:20951486	TACTTAAAAAAAAAA[-/A]GACATTCTTGTTTCT	10529
rs397845131	in-del	-/T			intron-variant	NEBL	GRCh38.p7	10:20992795	TTTTTTTTTTTTTTT[-/T]GAGGCGGAGTCTCGC	10529
rs397845282	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:20798126	AAAAAAAAAAAAAAA[-/A]TGTAGCATGGGCATA	10529
rs397845408	in-del	-/AA			intron-variant	NEBL	GRCh38.p7	10:21010614	CCATTCAAAAAAAAA[-/AA]TAAGAAAGCATTAGG	10529
rs397845446	in-del	-/T			intron-variant	NEBL	GRCh38.p7	10:20787858	TTTAAAGAAACATTT[-/T]ACTTAGAATATATGA	10529
rs397845505	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:20798126	AAAAAAAAAAAAAAA[-/A]TGTAGCATGGGCATA	10529
rs397845517	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:21160866	TTATTTCCAGGGGGA[-/A]AAAAAAAAAAAACAT	10529
rs397845667	in-del	-/A			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21144970	TTAAAAAAAAAAAAA[-/A]GATATCTCTCCAAGC	10529
rs397846529	in-del	-/T			intron-variant	NEBL	GRCh38.p7	10:21057567	TTTTTTTTTTTTTTT[-/T]GAGACGGGGTCTGGC	10529
rs397847147	in-del	-/T			intron-variant	NEBL	GRCh38.p7	10:20912901	TTTTTTTTTTTTTTT[-/T]AGACAGAGTCTCTCT	10529
rs397847419	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:21056418	TGGACCTGCAAAAAA[-/A]GATAGACTGACTGTC	10529
rs397847609	in-del	-/A			downstream-variant-500B	NEBL	GRCh38.p7	10:20779582	TGAAGAAAAAAAAAA[-/A]TCCCCTTTTACCTAC	10529
rs397897462	in-del	-/AG	0.169922	0.236828	intron-variant	NEBL	GRCh38.p7	10:20828783	GAGAGAGAGAGAGAG[-/AG]GTGGAGAGACAGAGA	10529
rs397934145	in-del	-/GG			intron-variant	NEBL	GRCh38.p7	10:20981602	ATAACATGACTTGGG[-/GG]ACTGGCTAATCAGAG	10529
rs397939963	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:20978768	CAAAAAAAAAAAAAA[-/A]GTTTGGAAAGGTGTG	10529
rs397942983	in-del	-/AACT			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20848625	ACCCTATTATGAACT[-/AACT]GTGCATGCAAGGGAT	10529
rs397959901	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:21035741	TTATTACCTTCAAAA[-/A]TCATACACATTTTCT	10529
rs397961227	in-del	-/T			intron-variant	NEBL	GRCh38.p7	10:21153338	AATTAATTTTTTTTT[-/T]AAGATGGAGTTTTGC	10529
rs397963723	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:21166070	TAAAAATACAAAAAA[-/A]TTAGCCGGGCCTGGT	10529
rs397966743	in-del	-/TG			intron-variant	NEBL	GRCh38.p7	10:20799949	GTGTGTGTGTGTGTG[-/TG]AGACGGAGAAAGAGA	10529
rs397974765	in-del	-/A			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20870345	AAAAAAAAAAAAAAA[-/A]CTTGAACTGAATTTA	10529
rs397976219	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:21024522	CCAAAAAAAAAAAAA[-/A]GAAGGCTTAACTATT	10529
rs398012973	in-del	-/TG	0	0	intron-variant	NEBL	GRCh38.p7	10:20947716	TTTGTCTCCTGACAC[-/TG]TGTGTGTGTGTGTGT	10529
rs398012974	in-del	-/A	0	0	intron-variant	NEBL	GRCh38.p7	10:21027338	TCTATCTGAAAATTA[-/A]AAAAAAAAAAACAAA	10529
rs398012976	in-del	-/C	0	0	intron-variant	NEBL	GRCh38.p7	10:21097229	TTGTGATCTGCCCCA[-/C]CCCCCCCCCGGACCT	10529
rs398054184	in-del	-/AA			intron-variant, upstream-variant-2KB	NEBL, LOC102725112	GRCh38.p7	10:20844524	AACATAAAAAAAAAA[-/AA]GCTTTTAAAGGTGGA	10529
rs398054185	in-del	-/AA			intron-variant	NEBL	GRCh38.p7	10:20978767	CTCAAAAAAAAAAAA[-/AA]GTTTGGAAAGGTGTG	10529
rs398054186	in-del	-/TTG			intron-variant	NEBL	GRCh38.p7	10:21074820	TTGTTGTTGTTGTTG[-/TTG]AGACAGGGTCTCACT	10529
rs398075000	in-del	-/A			downstream-variant-500B	NEBL	GRCh38.p7	10:20779581	ATGAAGAAAAAAAAA[-/A]ATCCCCTTTTACCTA	10529
rs398075001	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:20800724	ATATTTGAAAAAAAA[-/A]ATCTACCAATACTAT	10529
rs398075002	in-del	-/T			intron-variant	NEBL	GRCh38.p7	10:20807668	GCTCAACCTCAAAAT[-/T]TCCTACCTTTGGGAT	10529
rs398075003	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:20919976	AAAATTGAGAAAAAA[-/A]ATCAACAACCCAATA	10529
rs398075004	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:20995940	TATTATGAAAAAAAA[-/A]ATCTGCACCTCCATA	10529
rs398075005	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:21040346	TCCATTCAAAAAAAA[-/A]AGAAAGAAAGAGGGT	10529
rs398096840	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:21024826	CTCTCCAGCAAAAAA[-/A]GAAAAAGAAAAGAAA	10529
rs398114147	in-del	-/A			intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20898453	ACTGTAAAAAAAAAA[-/A]TGCCTTGGCCTTACC	10529
rs398114148	in-del	-/A/AT	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20925724	AATTAAAAAAAAAAA[-/A/AT]GGCAGAACAGAAGCT	10529
rs527245173	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20961120	ACTGAATTAATACCT[C/T]CCTAATACATTTTGA	10529
rs527260501	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20845626	ATCTTACTAGCCTAG[A/G]ATTAATATCAGCCCA	10529
rs527269988	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21162551	TTCCTTACACACTTG[C/T]TCTTTAAAAAGTAAA	10529
rs527270289	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20911272	CTGGAAAGTAAATTC[C/T]ATCAGGATCCCCAAA	10529
rs527310628	snp	A/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21088141	CACCCTGGGGCCCAG[A/T]TGTTTCTCTCCACAT	10529
rs527313489	snp	A/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20953853	TATTACCTCATTCGT[A/T]TATTCCACATGCATT	10529
rs527314572	snp	A/T	0.00279162	0.0372561	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21130938	TCCATACAGAAAAAA[A/T]TGTCAATGAAACCAA	10529
rs527325963	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21052155	ACCAAGAAGTGTTTG[C/T]GCTTTTTCCTTCAGA	10529
rs527331767	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20881991	GAGAGACTTGCTCAC[A/G]ACAAAGTGAGGCTCC	10529
rs527343556	in-del	-/AAAAATAAAAAAT			intron-variant	NEBL	GRCh38.p7	10:21062509	CTACAAAAAAAATTA[-/AAAAATAAAAAAT]AAAAATAAAAATAAA	10529
rs527345154	snp	A/C	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20799435	TGCTGGGATTGCAGG[A/C]GTGCCCGGTTCATCA	10529
rs527345824	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21045024	GCATTCTCAGAAGAA[C/T]GTTAATTATAGACTA	10529
rs527359372	snp	C/T	0.00716266	0.059414	intron-variant	NEBL	GRCh38.p7	10:20992373	GACACAGGCATGTGA[C/T]CTAGGCAGCATGAAT	10529
rs527363050	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20839577	AAAGTGCCTTTTAAA[C/T]GTTTCCTTTATTTAA	10529
rs527364696	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21094223	TTAGCCAGGTGTAGG[C/T]CGGAGACGGTGGCTC	10529
rs527366306	snp	A/C			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20870789	CTGAATGCATGTTAG[A/C]CACAAACCAAAGTAT	10529
rs527366681	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20876543	AATTGTTTACTGATA[A/G]GTTTTTATTAATTTT	10529
rs527367937	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21087492	TTTTTTCAGACTTTC[C/T]CTTCTCCCAGTTTTT	10529
rs527369970	snp	C/G	0.00398564	0.0444627	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20882624	TGAGCTTAAACTCTT[C/G]ATTGGCTTTTATAAA	10529
rs527388603	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20840015	GATTTTCTATTCCAT[A/G]AGTGAAGACATCTCC	10529
rs527390723	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:21160190	CATCACTGTATAAAG[-/A]AAAAAAAAAAACTAA	10529
rs527398968	snp	A/G	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21130049	TTAAAGTAAATGAAC[A/G]GAGAAAAAGATATCA	10529
rs527401914	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21051300	ATTTAAAAAACAAAT[A/G]CATAAAATTAGAAAT	10529
rs527413287	snp	A/T			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21141219	TATTGTTTCATTTAG[A/T]GAAATCTGAACGAGG	10529
rs527419595	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20992908	TCAGCCTCCCCAGTA[C/G]CTGGGACTACAGGCG	10529
rs527428519	snp	C/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20847767	GTTAACAGCTTCATA[C/T]TGTCTTAACCCATTT	10529
rs527431226	snp	C/T	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21144783	AGCCAGGTTCCAACC[C/T]AAGCCCCATCATATA	10529
rs527434004	snp	C/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20948853	AGGGGATGTCCCAGT[C/G]GTTTGTCGTTAACAC	10529
rs527434639	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20915490	AATTCCCACCTATGA[G/T]TGAGAATACATGGTG	10529
rs527439289	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20827411	GACATCTGACCAGCT[G/T]ACTCTGAGAGCTGGC	10529
rs527453365	snp	A/C			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20851148	TTCCAATAACAAAAA[A/C]TAATATGTAAGCCAT	10529
rs527453482	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21057241	ATGACACCTGGTTGG[A/G]AGAACAGTCTCCCGG	10529
rs527480628	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20985802	CGAAAATTATGTTTT[A/T]AAAAAAAACCAGTGT	10529
rs527495720	snp	C/G	0.00517822	0.0506191	intron-variant	NEBL	GRCh38.p7	10:20943187	AAGACTTGGAACCAA[C/G]CCAAATGTCCAACAA	10529
rs527504425	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21100033	CTTAAAAACACGCCC[A/G]ATAACCTGGCCTAAA	10529
rs527511139	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20787979	TCCTTAAAGAATTTC[A/T]TAAACATTATTCTTC	10529
rs527512728	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20794242	GAGGAAGTGTACAGC[C/G]TAAAATATCTTTGCA	10529
rs527513360	snp	C/G/T	0.00677167	0.0578647	intron-variant	NEBL	GRCh38.p7	10:21017969	GGGATTACAGGCATC[C/G/T]GCCACCACTCCCAGC	10529
rs527514623	snp	C/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20827800	AGCTAGATGCCATTA[C/T]ACTTAGCAAACTAAT	10529
rs527537569	snp	A/G	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:20935390	AGTAAGGCAGCAGAC[A/G]ATTATCAGCATCTCT	10529
rs527540875	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20823143	TGACCTGTACAGGTT[C/T]TATGCTGTCATTACG	10529
rs527542227	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20980496	ACACCTGCAGTGCAC[A/G]TACAATCGTTGGTTA	10529
rs527549266	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20903971	ATGATAAAATTCATC[C/T]ATATAACCAAAAACC	10529
rs527558623	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20943495	CCTAATGTTAATTGA[C/T]GAGTTAATGGGTGCA	10529
rs527558820	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21150286	ACGGTTGGAAGCTTT[C/T]GCTTCTCATCAACTT	10529
rs527560161	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20938452	GTACATCACCATCAT[C/T]AAAGACCAAAGGTAG	10529
rs527578962	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21069289	TCCCTTCGTTTTTCA[C/T]AATCTCTCAAGAAAG	10529
rs527583389	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20863758	CCTGCCTTGTGGGAA[A/G]TGAAATGGATTTCGA	10529
rs527583883	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21023693	GAGTGAGACTCCATC[A/T]CAAAAATAAATAAAT	10529
rs527588766	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21035463	AACTCAATAAGCAAA[G/T]CACACTTTCTTCCTA	10529
rs527599406	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21104545	GCTTATTGCCAGTAC[A/G]TAGAAATGCAAATGA	10529
rs527601814	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:21078606	ATACACGTATGCAGA[C/G]GTATCTACTCCTATG	10529
rs527604667	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20796800	ACCACAAATATAAGC[A/G]GGATTGTCGGTGAGG	10529
rs527613286	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20821767	TGTGGGAATCCATAC[G/T]ACCTTTTTGTGATCT	10529
rs527615374	in-del	-/A	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20805495	GCAATGTCCCTAAAG[-/A]CAGAGCATCTTGGCC	10529
rs527615523	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21033599	ACAAAAATTAGCCAG[G/T]CATGGCGGTGTGCAC	10529
rs527617308	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20858031	GTTGTATGCAGGAGA[C/T]ACTGGAGAGCAAGCA	10529
rs527621839	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21027240	AGCACAGGCCCCTTT[G/T]TGCGTAACAGGCTTT	10529
rs527624594	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20934023	TTTTAAAATATGTTT[A/T]CATTAATGTTGAAAT	10529
rs527642715	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21156193	ATTCATGTAATTTGC[A/G]AGAAGTAGCTTTGCC	10529
rs527642765	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21149694	CAGAGTTCTGGGAAC[C/T]CTGATTAATAGCCCG	10529
rs527662327	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20975298	GGTTGACATGGATAA[G/T]TGTTTCGACTTCTCT	10529
rs527672988	snp	C/T			intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20898324	GGGCATAAAAAATAC[C/T]CTACACTGAATAGTA	10529
rs527678199	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20893909	GAAATGGCTCTGATG[A/G]TCTACAGATTATCAA	10529
rs527684501	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21110128	TCTTTCCTGTTTTCT[C/T]CTGTGGACAATGTTC	10529
rs527687644	snp	C/G	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20934535	ACTTCCAGACTGAAC[C/G]TGAAACCCGTGCTAT	10529
rs527694420	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20810443	CCTAGTTTTCATTCT[C/G]AGTCTGTGAGTGCAA	10529
rs527701719	snp	G/T	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:21074671	TTTCAGTAGAGACGG[G/T]GTTTCACTGTGTTAG	10529
rs527704527	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20852448	CTTTTCTGCAACTGT[A/G]CTTTCTCAGTTAAGA	10529
rs527708994	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21121509	CCTTCCAAGTTGTCA[A/T]AGGAAAAGTCCAAAT	10529
rs527715768	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20894434	GCTGCAGTCACATGA[C/T]AGAACTCCAGCCTGG	10529
rs527715970	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21011068	TTTTCAAGTTCTTTT[A/G]TTGCTACATTGAGAC	10529
rs527727384	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20969131	CTCACAATGTTAGAC[A/G]GGAATTAAACAGTCG	10529
rs527736686	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21038725	CCTTTGAGTATATAC[G/T]CAGTAATGGGATTGC	10529
rs527746204	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21116265	GGTTGGAAGTCCAAA[C/T]TCAAGCTGCCAACCA	10529
rs527749194	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20917354	TCTGAACTATTTCTC[A/G]AGGGGCACAAACCCA	10529
rs527756347	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20811274	AATTCTGAGAGCCCA[C/T]GGTCTAGACAGTTTC	10529
rs527765221	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21005370	CAGCCTGAATGGTAA[A/G]GCCTCAGTGTTACTG	10529
rs527772486	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21162512	ATCAGAATTGCATTG[C/T]GGTATTGTAACACCC	10529
rs527789053	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20969714	CCACACTGAGCTAAT[C/T]TTTGAATTTTTAGTA	10529
rs527799597	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21038225	TTATTTTAAGTTCTG[G/T]GATAGATGTGCAGAA	10529
rs527799716	snp	C/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21044258	AAAAATTAGCTGGGC[C/G]TGGTGGTGGGCGCCT	10529
rs527802026	snp	C/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20882446	TCAATGAAAATAATA[C/T]ATAAAATTAAATTTA	10529
rs527803706	in-del	-/AAAAAAAAAAAAAAAAAAAAA			intron-variant	NEBL	GRCh38.p7	10:20997494	AAAAAAAAAAAAAAA[-/AAAAAAAAAAAAAAAAAAAAA]CAGAACTCCTGAAGA	10529
rs527826663	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20847119	TGGGAATAAAAAAAC[A/T]TCTCTAAGACAAATG	10529
rs527827831	snp	A/C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21086694	AGGTGGGTGGATGAG[A/C/T]TAAGCCAGGGAGGTG	10529
rs527829877	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21079955	ATCCTCAGAGAGGGG[C/T]GGAGTATAGATACTG	10529
rs527830073	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20929630	AACTGGAGGCCATTA[C/T]CGTTAAGTGAAATAA	10529
rs527833123	in-del	-/CTCCT	0.0111196	0.0737302	intron-variant	NEBL	GRCh38.p7	10:21163804	CTAGTTCTCTTCTGG[-/CTCCT]CCTAGAATTCAATAA	10529
rs527846423	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20883349	TCACATTGTTCCAAG[A/G]ATAATTCATCTTGTT	10529
rs527858916	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21159151	CCCTTTCTCTCTCTG[A/G]AATAATTAACACTTT	10529
rs527862009	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20840644	AATCACTTACATATA[A/G]AAGTTATAGATGTAT	10529
rs527867482	snp	C/T	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:20829325	ATCATTCTCAGTAAA[C/T]TATTGCAAGAACAAA	10529
rs527868990	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20805839	GGCTGAGTGACACAG[C/T]GAGACTCCGTCTCAA	10529
rs527872280	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20976973	TGTACCTAAACAAAG[A/G]AACATAGCCAACCAA	10529
rs527875378	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21122214	TATTTTTAATAGAGA[C/G]AGGGTTTCACCATGT	10529
rs527878525	in-del	-/ACTGC	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:21104733	ACTTTCTCCTGCCTT[-/ACTGC]ACTGATAAGAACTTC	10529
rs527887010	snp	A/G			utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20780154	TCAATTATGGGAAGC[A/G]TAGTGGGGGGAGAAA	10529
rs527891459	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21092558	TACTATATTTTAATT[C/T]ACATGGACTTCTTTT	10529
rs527905088	snp	C/T	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21136681	TACCCTACGGCTGGA[C/T]AAAGCTCGCCAAAGC	10529
rs527907051	snp	A/C	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21128637	AAAAGAAAGTTCAGA[A/C]TGGAAAGGGCGAGAG	10529
rs527937308	snp	C/T	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20800667	TTCAGTGTTTCTGCT[C/T]TTCTGCATAAACGAC	10529
rs527940668	in-del	-/A/AA	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:21086031	ATAAGATGTACTTTG[-/A/AA]AAAAAAAAATCCATA	10529
rs527948412	snp	A/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20801221	TTATTTTTATTTTTT[A/T]TTTTCTTTTGAGGCA	10529
rs527948895	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20841197	TTTGAAAGTTCTATA[A/T]AACATGCATTACCAA	10529
rs527951723	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20916979	TGCATATAATTTATA[A/G]TAAATATAAAATATC	10529
rs527954688	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20994342	AAAGTACAGGGAAGC[C/T]AACTCCAGGGGGATC	10529
rs527962097	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20878448	TTCCACTAGTAAATT[A/C]TCTGCAATGAGTTTC	10529
rs527972685	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20950120	ATATACAGAGCTTGT[A/T]GCTCTAACATTGTCT	10529
rs527982864	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21013074	ATTTTATCCAGGGGT[A/G]CAATGGGGGCGTGGG	10529
rs527985605	snp	C/T			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21130025	TTAAACACAAAGTCA[C/T]ATATACATTTAAAGT	10529
rs527988526	snp	A/G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21154967	GCACTTTGGGAGGCC[A/G/T]AGGCGGGTGGATCAC	10529
rs527991753	snp	A/G	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21135867	TTCCTCCTCAAACCC[A/G]GCCAGGATGAGAGAT	10529
rs527994714	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21162403	TGGTCCAAACTGTAG[A/G]TGACCTAGGGACTCC	10529
rs528010024	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20962132	AAGTACTCCATAATA[C/G]TTATTATGATTATCA	10529
rs528018152	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20987668	TCTGAGACTGAAGGG[A/T]TTATAGCAATGCGGG	10529
rs528021790	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20835389	GCTTCGGAATAGTCT[C/G]CATTCCAAACTGTTA	10529
rs528034224	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21020403	CCAGACATCCTCACT[C/T]TCTCCCACAGCTTAA	10529
rs528043561	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21072605	TGCGGAGCACAGGAA[A/G]GGTATGCCCAGGGGG	10529
rs528046564	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21013652	GGAGGCCAAGGTGGG[C/T]AGATCACTTGAGGTC	10529
rs528050149	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21153551	GTATTAATTTTGAGA[C/T]GGAGTCTCACTGTAT	10529
rs528058449	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21066285	GAATGTTGCAGTTGT[C/T]GAAAAAAAATGTTAA	10529
rs528060652	snp	A/G	6.70331e-05	0.00578896	synonymous-codon, intron-variant, missense	C10orf113, NEBL	GRCh38.p7	10:21126099	CCTCAGGCCCTTCTC[A/G]GCTCTCCGTTCTGCC	10529
rs528070096	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	NEBL	GRCh38.p7	10:20819282	TCCATGTATTCTCAT[C/T]ATTTAGCTCTCATTA	10529
rs528070880	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21114337	AGATTTGTTTTATGG[C/T]CCAAAATATGGTCTA	10529
rs528072294	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20971358	TGCTTCTGAACACAT[A/G]TTCTCTTAATCCTTT	10529
rs528078176	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20901875	ACTTTACTGATGGAC[A/G]AGGCAAGATAAATCA	10529
rs528086355	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21030589	TACCCTACAAGTGGT[A/G]GGGGAAAAGTAACTC	10529
rs528087060	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21159643	ACATTTCCAATCTGG[A/C]CAAGAGGCACATGGT	10529
rs528088804	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21107729	TACAGATTGAAATAG[C/T]TTTGGAAGGAATGGT	10529
rs528091504	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20854775	CCACTACGCTGCCCA[C/T]GCTGGTCTCAAACTC	10529
rs528095908	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21014154	TTAGATTTAGGGTCT[C/T]ACTCTGTCACCCAGG	10529
rs528096488	snp	A/C			intron-variant, downstream-variant-500B	NEBL, LOC102725112	GRCh38.p7	10:20885345	TATGACAGTTACATA[A/C]ATCTTTGAAGTAGCC	10529
rs528100142	snp	A/C	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20936374	GTCTAGTCTGTCTCT[A/C]AAATCAGCTGTTTAT	10529
rs528108852	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21047697	TAACCTGAACAACTA[C/T]TGTATGAATCAGAGG	10529
rs528121304	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21072253	AGTCTCCTCATAGCC[A/C]TCCCTTCTGCATCTG	10529
rs528126089	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21020539	CCATCCTCCAACCAA[A/G]CTTCCTGACAAAGAA	10529
rs528133707	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20972233	TCTCGTCACAGCTGA[C/T]AAAAGTGACAGATTA	10529
rs528136414	snp	G/T			intron-variant, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20879621	CTATGGGGGCACATG[G/T]TCAGCCAAGCACCAT	10529
rs528136878	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21036227	GCATTTTGGGAGGCC[A/G]AGGCAGGAGGATTGC	10529
rs528141027	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21120616	CATAAAATACCGGTT[C/G]TCTCTCCCATCATCC	10529
rs528143041	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20855161	CTTGAACCTGGGAGC[A/G]GAGGTTGCAGTGAGC	10529
rs528156133	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20809194	ATAGCTATCTATTGT[C/T]TAACATAACTGCATA	10529
rs528164655	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20831192	ATCTTCATTCATGAC[C/T]AACCTGGCTATAGAT	10529
rs528177020	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21119850	AGGATCACATCCTAC[A/G]TTTAGATGTCATATC	10529
rs528178246	in-del	-/ACTC	0.0142736	0.0832652	intron-variant	NEBL	GRCh38.p7	10:20957209	ATATTGTTGAAGCTA[-/ACTC]ACAAAATCTCAGGGA	10529
rs528188083	snp	C/G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21159146	ATTCCCCCTTTCTCT[C/G/T]TCTGAAATAATTAAC	10529
rs528199055	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20972617	CTGGGCATGGCAGTG[C/T]GCACCTGTAGTCTCA	10529
rs528205747	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21066260	CTTTTACAGACCCGA[C/T]ATAGGATAGGAATGT	10529
rs528231563	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20999334	GGATGCAGTGGCTCA[C/T]GCCTGTAATCTCAGC	10529
rs528241157	in-del	-/AAAAG	0.00199481	0.0315187	intron-variant, downstream-variant-500B	NEBL, LOC102725112	GRCh38.p7	10:20880360	CGAGGCTCTGTGTCA[-/AAAAG]AAAAGAAAAGAAAAG	10529
rs528242150	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20958831	CCCAGAAAAGGCAAG[C/T]TCACCCACTCTCACC	10529
rs528247270	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20892094	ATTGGATAGACTGGC[A/C]ACTCCCATTATCTCC	10529
rs528251564	snp	C/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21077201	ACAGTACTTAAAACT[C/G]ATGCTTAATCTACTT	10529
rs528251967	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20843225	AAAGGTGTCTGCAAG[C/T]CGGTAAGAGGGCCCT	10529
rs528255025	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20966279	CTTCCTGCAACATAG[A/G]TTAGAACGCTAAAGC	10529
rs528255944	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20886145	GTTTACCTATGTAAC[A/C]AATCTGCGCATCCTG	10529
rs528257552	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21041208	CTCACTCTCCTCCCA[C/T]GCTCCACCCTCAAGT	10529
rs528261087	snp	C/T	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21126358	GATTAGAGTGTGGAC[C/T]CCTCTCAAGCCAGTG	10529
rs528263892	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21171305	ATGCCATTGCACTAC[A/G]GCCTGGGCAACAGGA	10529
rs528266495	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21119268	TCTTCCTAACTTTTT[A/G]TTTTGAAAAATTTCA	10529
rs528283656	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20925647	CAACTCCTTAACCCA[C/T]ACATTTAGAAAGATG	10529
rs528288785	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:20841839	GGAAGGCTGTCTCCA[A/T]GCAATTTAAAGAATT	10529
rs528289232	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20919009	GGAGGTCAGTAGTAG[A/G]ATTCTGGAATATTTT	10529
rs528299711	snp	C/T	1.64798e-05	0.00287047	synonymous-codon, intron-variant, utr-variant-3-prime	C10orf113, NEBL	GRCh38.p7	10:21125958	CTTGGCCCAGTTGCC[C/T]GGATCTGGTTCAGGA	10529
rs528301650	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20952143	AGTTTTAAAGGTTCA[A/G]TTAAGAACCGGGGCC	10529
rs528306781	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20996569	TTTAAGTAACTTGTC[C/T]GAGGACACATAGTAT	10529
rs528317123	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21083555	TATATACCGCTCCTC[A/T]CAGAGAAGTCCTCGG	10529
rs528319719	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20808389	TTCTGAACTTAATTT[C/T]AAATTCTCAAATACA	10529
rs528321914	snp	C/T	0.000798403	0.0199641	intron-variant, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20880104	ACGGTGGCTCGTGCC[C/T]GTAATCCCAGCACTT	10529
rs528323425	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20933382	ACTTACCCGTACACT[A/G]CTAGACTATATGACT	10529
rs528339058	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20919611	AGGACAACCCCTTAA[C/T]AAATAATGTTACAAC	10529
rs528343594	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20886531	AAGACTCCATCTTAA[A/T]AAAAGAAATTCTGGG	10529
rs528344505	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:20887653	AACTCCTGAGCTCAA[G/T]CATTCTGCCCACCTT	10529
rs528353872	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20797793	AGGTATGGCACAAGA[A/G]TAAGATCAAGGACCA	10529
rs528362982	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20952665	ATCCCAACACTTTGG[C/G]AAGACGAGGTGGGCG	10529
rs528368293	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20997051	AATCCATCTTTCTAC[A/C]CTGTAACTGAACATA	10529
rs528372063	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	NEBL, LOC102725112	GRCh38.p7	10:20880393	AACAGTAGTGGGTAC[A/G]ATATAGCTGGTGTTC	10529
rs528420494	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20947136	TGAAAGTCTGTTTCT[A/G]AATGACTGGGAATTT	10529
rs528430650	snp	C/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20990773	TCACCCAGTGTGACT[C/G]AGTCACTAATCTTCA	10529
rs528432523	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20997819	TTTAAAAATCAGTAA[A/G]CTCAGAAAACATGAG	10529
rs528434937	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20913458	TACTTATTAAGAGAT[C/T]GTTACGTGAATTAGG	10529
rs528440424	snp	A/G	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21139800	GTCTATGAAAGCCAC[A/G]GTATTAATAACTTTG	10529
rs528462286	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20874941	GATGAGGTTTATCAT[A/G]TTGGCCAGGTTGGTC	10529
rs528466926	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21059587	AATATTCTCAAATTA[A/G]TTTTAACAGCTGGAA	10529
rs528467168	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20837647	GCAGACAAACCAGCC[C/T]TCTATTGGAAAAAGA	10529
rs528471309	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21054432	GCCCCAAGCATTTCC[A/G]GGTCATTCTGATCTA	10529
rs528475077	snp	C/T	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20807868	CCCTAAAGAAATTCA[C/T]TGAAGTTCTAGGCTT	10529
rs528492115	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20941742	AACTTCAGCAAAGTC[G/T]CAGGATACAAAATCA	10529
rs528498299	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20832024	TTTGCCACTAGACAA[C/G]TCAATGTTCCCACTC	10529
rs528516503	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20792304	GAGTCTAGGACACAA[C/T]GCAATTATTGTCATA	10529
rs528526250	snp	A/C	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20978492	CTGGGTGCAGTGGCT[A/C]ACATCTGTAATTTCA	10529
rs528529270	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21058921	ATTGTGTAAAGTTGA[A/G]CAGGTCAAAGGTTCT	10529
rs528548420	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21029914	GACCGATACAACAGA[G/T]GGGATGATGGGTCGT	10529
rs528551900	snp	C/T			intron-variant, downstream-variant-500B	NEBL	GRCh38.p7	10:20815278	ACAATCCATGTTCAA[C/T]GAAATATTTCAGGAA	10529
rs528556168	snp	A/G	0.000798403	0.0199641	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21146030	AAAATGGAGTGGGAA[A/G]GCAAAGAGGAGCATT	10529
rs528568462	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20780024	CCGCAAAGTTTATCA[A/G]TTTACAATTAGGAAG	10529
rs528569290	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21071629	CTTTTTAAATGTTCT[C/T]CAGGTGATTCTAATG	10529
rs528579521	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20786696	TTGAGGGCTTGTAGA[A/C]GAAATTTCTGCATGA	10529
rs528580194	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21094985	ATCCAAAGTGTAGGT[A/G]TGCCTATATCCATAG	10529
rs528583035	snp	A/C	5.72902e-05	0.0053518	intron-variant	NEBL	GRCh38.p7	10:20787151	GTATTTACATGCTTG[A/C]GGGGAAATGGGAAGA	10529
rs528589883	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21021956	CAGTCAAACTTCAGC[A/G]TGTCCTATAAGGCAT	10529
rs528596289	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20862251	AAATGTAATAATAAG[A/C]ATTGTATTGTGAAAT	10529
rs528600744	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:20966379	TCCTGATCCTCAGAA[A/T]ATAAAACAAGAAAAT	10529
rs528608217	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20979145	ACGTAGGACTGGGCA[C/T]GGTGGCTCACGCCTG	10529
rs528613633	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21112639	AAATACCTAATGTAA[A/G]TGACGAGTTGATGGG	10529
rs528615292	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20818107	AATAGAAGCTAAAGC[C/T]CTCTGACTCCTACCA	10529
rs528618697	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:21025274	GATGTGGGGAATATG[C/G]TGAAATGTTTAGCAT	10529
rs528623790	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20952725	GCCTGGTCAATATGG[C/T]GAAACCCCATTTCTA	10529
rs528628389	snp	C/T	0.00199481	0.0315187	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20780690	TGTAGAGATAGGAAA[C/T]TAATGTGTTATAATG	10529
rs528629794	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20820117	TTGGGAAGGAGAGTA[A/T]CAAAATCCTGTACCT	10529
rs528638768	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20973476	GCTGGTCTCAAATTC[C/T]GGGCCTCAAGTGATC	10529
rs528643509	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21070934	GTAACCCCAACACTT[C/T]GGGAGACTGAGGTGG	10529
rs528647722	snp	C/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20865670	GCATTACTGGGAATA[C/T]GTAGAGCTTAGAGTC	10529
rs528652539	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21022381	CAGTAATCATTTGTC[A/G]GTGCAGATAAAGCCT	10529
rs528652903	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21074646	CCAAGCTCGGCTAAT[C/T]TTTTTGTACTTTCAG	10529
rs528670977	in-del	-/A	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21151497	GTGCTTTATTTTTAC[-/A]AACCAGCCAAAGTGA	10529
rs528678878	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20898408	GCCAAGCATAATTTT[G/T]TCTCTTGATATCATA	10529
rs528696198	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21009429	ACAGGAGCTCAGTGT[C/T]AGTCAAAAGGGGTCC	10529
rs528700840	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20967349	ATGTAGACACAGGGC[C/T]GGGCATGGTGGCTCA	10529
rs528700961	snp	G/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20974134	CTGTGAATAGTAGAG[G/T]CAGGATTCAAACCCA	10529
rs528702162	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20891935	TTAGTAGCCTTCCTA[C/T]ACCAAGATAACAGGA	10529
rs528714275	snp	A/G	0.00835141	0.0640778	intron-variant	NEBL	GRCh38.p7	10:21016074	GGCTGCTGCGGGCCC[A/G]TGGGGGCGTCTAACC	10529
rs528729161	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20868819	CCTCCAATGATGAAC[C/T]ACATTGACATTAGCC	10529
rs528741121	snp	A/G	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:21111538	AAACTGGCTAGCCAC[A/G]TGTAGAAAGCTGAAA	10529
rs528753209	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21040489	TGTTACCTGGTGAGC[A/G]AAGGAGAAATAGAGG	10529
rs528753268	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21034486	AGGCACCTGTTGCCA[C/G]ACATCCTAGAGCACA	10529
rs528759648	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21003759	AGGAATGTAGGAAAA[C/T]TGTCATATAATTCTG	10529
rs528763404	snp	C/T	0.00953873	0.0683987	intron-variant	NEBL	GRCh38.p7	10:20831918	GTCAGTCAAGAGTGA[C/T]TGTAAAATTGCTGTT	10529
rs528796223	snp	A/G	0.000798403	0.0199641	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21125340	CACGAGCTCCTTTTT[A/G]CATCATAAGACTCCT	10529
rs528796867	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21170488	TTCCCTTCTCCTTAC[A/G]CCTGCCTTTGATCTT	10529
rs528800854	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21046210	AAAGCAGAAAATGGT[A/G]ATTACCAGAGGCTGG	10529
rs528822129	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21015027	ATCGTATCTGCCCTC[A/C]TAAATTACACATACT	10529
rs528831642	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20949468	TAAAGTAAAAAATAA[A/T]AAGAAATTCAAAAGT	10529
rs528837057	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20911057	TAGTTCCAGCTGCTC[A/G]GGAGGATGAAGTGGG	10529
rs528843501	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20834710	CCCCTTCACCTGCAC[C/T]CCGATTTTTTCTTCA	10529
rs528844850	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20927085	AGTTTCAACGCGACT[A/G]CATGTGGAGAGACAG	10529
rs528848169	snp	A/G			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20865683	TATGTAGAGCTTAGA[A/G]TCACCGCCCTTTAAT	10529
rs528848409	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20889817	AAAAGATAAATGCAA[A/G]CCAGTTTGCAAGCTT	10529
rs528848498	snp	C/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21023692	AGAGTGAGACTCCAT[C/T]TCAAAAATAAATAAA	10529
rs528862448	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21158517	TGTAGGTGAGGAAAC[C/T]GAGGGATGGTGAGGC	10529
rs528870087	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21112804	AGTGATTTCCCTTGG[G/T]GGCTTTGAAATTACA	10529
rs528877697	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20986758	TGAGTATGAATTTCT[A/G]TGATAGATCCTAAAT	10529
rs528880895	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21119648	GCATTATGACAATTA[A/G]GTCATAAATGCTTCA	10529
rs528881982	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20878372	CACACTTTTATTTTA[A/G]ATTAAATGAAGTCAT	10529
rs528886950	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21165726	TCCTGCACAGGGTGG[A/T]GTGGGCTCTTACTGC	10529
rs528892298	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20950048	CCCTCTGATATTAAC[A/G]CAGCATTTCCCTCTA	10529
rs528897147	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21077073	ACGTATATCTTACCA[A/C]AATTTAAAAATATGT	10529
rs528906011	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20835352	GCAAAGCAAAAACTG[C/T]AATTTTTCAAACTGG	10529
rs528911914	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20999579	ACTCCAGCATGGGCA[A/G]CAGAGTGAGACCCTG	10529
rs528915003	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21025559	GACCTCGTCAGAGCT[C/T]GTCAAAATGCAGGAA	10529
rs528918342	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20943744	TCGATTCCTTACACA[C/T]GTAAAACTAAGTCGT	10529
rs528918921	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20828384	AAAATTATCAGTATT[C/T]TTATTATTTTAAAGA	10529
rs528925531	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20794930	ACAATCTTCTTTTCA[C/T]CAACAAAGGAGCTGA	10529
rs528928806	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21023884	AGTAATGAACTTCAC[C/T]TGCTGCCCATACCAC	10529
rs528938451	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20795349	GTGTGTATATGTGTG[C/G]TAAACATCCAACCAG	10529
rs528941572	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20987584	CAGAGCCACAGACTG[C/G]AGCATGGTGCCAATA	10529
rs528944945	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20904642	GCAAATGTCACATGT[C/G]TGCTTGTACATATGT	10529
rs528954013	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20905753	GAACCAAAAGTTCTA[C/T]GTCACTGGAGCAATA	10529
rs528959029	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21083417	TTGTAGCAATGATCT[G/T]TTCAAGGGGTACACT	10529
rs528976249	in-del	-/TAAA	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20986712	TTCTCATTTCATGTT[-/TAAA]TAAATGACAGAGAAA	10529
rs528976351	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20783208	CTTTTAAAAATAGCA[C/G]TTTGGTTTTATACAT	10529
rs528976366	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21040586	CTCATTACCATGGGG[A/C]GGACACAAAGCCATT	10529
rs528977558	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20944261	AAAAATTAGCCAGGC[C/G]TGGTGACGGGTGCCT	10529
rs528981630	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20904985	ACAGCAATGTAAATA[C/G]TTTCCTAGTAATTTA	10529
rs528982211	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:20887844	AGCTGTCTAAATGAG[A/T]TTAAGATTTGCTCTA	10529
rs528982749	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21171697	ACACGGTGAGCGCGA[A/T]ATAAATGCTAGCTAA	10529
rs528984659	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20900323	GGCAAATTATTCAAC[A/C]CCTCACTACCTCTAA	10529
rs529007538	snp	C/T	2.17233e-05	0.00329563	intron-variant, utr-variant-5-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20897227	CCTTTAAAATATTTA[C/T]ATTTTTAAAATTTAC	10529
rs529017867	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21171265	GCTTGAACCTGGGAG[A/G]TGGTGGTTGCAGTGA	10529
rs529034019	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20889695	ATGAGTTAAATGACA[A/G]CGCATCACATTAGAT	10529
rs529034046	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20976255	CTGAGGCAGGAGAAT[C/T]GTTTGCACCCAGGAG	10529
rs529035073	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20822586	GATATATACAGACTA[C/T]CTAATATAGACTATA	10529
rs529037064	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21089184	AGTCTAGAGGATGCT[A/G]ACATTCAGGAACTAG	10529
rs529038277	snp	A/C	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21046349	GTATTTTATACTTGA[A/C]AATTGCTAGGAAAAT	10529
rs529041870	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20939048	AACTTCCCCAATCTA[G/T]CAAGGCAGGCCAACA	10529
rs529048483	in-del	-/AA/AAA	0.466618	0.124806	intron-variant	NEBL	GRCh38.p7	10:21048451	TAATAAATTTCTACC[-/AA/AAA]AAAAAAAAAAAAAAA	10529
rs529056932	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21053316	CAGACTTCTTGGCTA[C/T]AATCCCACTTCCCAC	10529
rs529059313	snp	A/C	0.000399281	0.0141238	intron-variant, nc-transcript-variant	NEBL	GRCh38.p7	10:20818930	TTATTAAATCTGGAG[A/C]TATTCCGTTTATCAT	10529
rs529065519	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20900718	AGTAGATGGGATTAC[A/G]CCTGTAATCCCAGCT	10529
rs529068567	snp	C/T			upstream-variant-2KB, intron-variant	C10orf113, NEBL	GRCh38.p7	10:21147808	AGCCCCTTCAGCATT[C/T]GGACTTGAGGCTGCA	10529
rs529076094	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20979673	ACATAATGTTTTAAG[C/T]AAACATAATATAACA	10529
rs529076136	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:20952949	AAAAAGAAAAGAAAA[G/T]AAAAGAAAAAACAAG	10529
rs529077457	in-del	-/ATTT			intron-variant	NEBL	GRCh38.p7	10:21034986	TTTATTTATTTATTT[-/ATTT]TTGAGACAGAGTCTC	10529
rs529084427	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20783861	TGGCCATTTCAGTGA[C/G]AGAAAACCAGCCAAA	10529
rs529105222	in-del	-/T	0.00557542	0.0525036	intron-variant	NEBL	GRCh38.p7	10:20886035	TTCAAGAGTAATGTA[-/T]TTTCAGACTACTTAA	10529
rs529107049	snp	A/C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21088777	TCTGGACAACCACTA[A/C/T]CAACTGGCAGAGGCC	10529
rs529107204	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21095251	TCCATCCAACAGGGA[A/G]TTATCTAGGGAGTGG	10529
rs529113700	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20900900	GGCACACACCTGTAA[C/T]CTCAGCTACTCAGGA	10529
rs529125526	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20934997	TAGTGAAGCAAAGTG[C/T]CACACGATTTTATTT	10529
rs529127393	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20969868	CACCTTTCAATTTCT[C/T]AATCAGTTAAGATAA	10529
rs529129223	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20820810	AGCCTGGGTGACAGA[A/G]TAAGACTCTATCTCA	10529
rs529140347	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20791047	AGTTTGAGTTTGACA[A/G]GTTGTTTTATGTCAA	10529
rs529141948	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20859510	TGCAACACTATTCCT[A/G]CTTATTAACTAATTA	10529
rs529158443	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21085300	TGTGGAATTTTTCCA[A/G]TTGTGCATTTTCAGT	10529
rs529159415	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21012787	ACAAACAGCCTAGAG[C/T]CTGCCCACCCAAAAT	10529
rs529171120	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21006130	TTCCTTCCTTTAAAT[A/G]ATCGCATCATATTCT	10529
rs529191645	snp	A/G	0.00358779	0.0422022	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20872649	GTCACAGAATGAGAT[A/G]GGAGGTTGGCAAAAG	10529
rs529198340	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21058736	AAGGGAACTTAAAGA[C/T]ATTTCAAACATCCTT	10529
rs529206910	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21109995	GGGTTTTTCATGCCT[C/T]TATCTCCTTCACTTC	10529
rs529212211	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20922904	TGATAATACCAAACA[C/T]ACAGAAACCGATGAC	10529
rs529217163	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21006516	AATCCAACCAGTCCT[A/T]CTTCCCTGTTCCTTC	10529
rs529241095	snp	A/G	0.00398564	0.0444627	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21145903	CATTAGGTGAGGCTC[A/G]GCTCTCTGGACCGCA	10529
rs529249190	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20884405	AAATTGGGGGTTTCA[C/T]AGATGCCCTGAAGCT	10529
rs529254224	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21029233	CCCACTGCTCCACCG[C/G]CTGCTCGGGAACCCA	10529
rs529276617	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21106550	ATTGGTCTATATATC[A/T]GTTTTGGTACCAGTA	10529
rs529282491	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20911239	CACATCTTATCTCAT[A/G]AAATACTCATAAACT	10529
rs529284275	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20841516	AAGGCCCCCTTTACT[A/C]TCTCTGATGGAATCT	10529
rs529284503	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21099012	GTGGCACACACCTGC[G/T]GTCCTATCTACTCGG	10529
rs529301344	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21112123	GTGGAGAAATAGGAA[C/T]GCTTTTACATGGTTG	10529
rs529317571	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21001369	AGAATCCAGGGAGGT[A/G]GAACACAGCCAGAGT	10529
rs529320754	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20917564	ATGCATCACGTACCT[C/T]ATTTTTAACTTGGAT	10529
rs529320791	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21105970	TCATGTGTCTGTTGG[C/T]TGCATAAATGTCTTC	10529
rs529330847	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21151845	ACCAAGTGAAACTTA[C/T]CTCTTCCCCTGCTCC	10529
rs529332192	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20954496	TGTTGCAGGACTTTT[C/T]CTTAGTTCAGCTAAA	10529
rs529332305	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20822711	ACTATAGATACGTAT[A/G]TATGTCTACAAAACA	10529
rs529336047	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20956853	GTAAGACCTAATTGC[C/T]TCATACACGATAATT	10529
rs529342502	snp	G/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21063832	CCAAGGTCACGCCAC[G/T]GCACTCCAGCCTGGG	10529
rs529350453	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21120911	CTATTGTGTAAGCTG[C/T]GGATGTTTACCATAT	10529
rs529365960	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20802171	CAATACCAGAAAACT[G/T]CAAGTTAAGGAAAAC	10529
rs529373053	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20842022	GTATGAAAATCATAA[A/T]TATCTTATTCCTATT	10529
rs529374729	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:20932578	ACATGTATCCCAGAA[C/G]TTAAAGTAAAATTTT	10529
rs529387903	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20796380	AAGAAAAAAAAAAAA[A/G]AAAAAAAAAAAAAAC	10529
rs529389678	snp	A/T	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:21074792	CATATAGATATATAT[A/T]TTTTTGTTGTTGTTG	10529
rs529395591	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20950913	TTTGCTAAACACAGG[A/C]AAATTCTAACACCTT	10529
rs529415041	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21031696	ATGACTCTGCTGCCT[A/G]GGCAGTTTCTCCTTC	10529
rs529417949	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21034445	AGTCCAGAAAAGATC[C/T]AACATTCTTCTCAGC	10529
rs529422946	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20912123	CTGCAAATATGAATG[A/T]AAATGTAAAAACATG	10529
rs529440817	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21076044	AAATAACAGGGTCTT[C/G]GTGAGGATGTGGAGA	10529
rs529440908	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20945093	ATTAGTATTTGCAGC[C/T]CATTAAACACCACAC	10529
rs529458733	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21033885	TTTAAAAAACACCAG[C/T]CTGGGCACAGTGGCT	10529
rs529464787	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20879539	TTTTTTACTTAAACA[C/T]TTGCTTACTGCAATT	10529
rs529478237	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21075555	TTTGTCCTTGCTGAG[C/T]CAAATCCTTCCAGAA	10529
rs529478304	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20945875	CTTGGACTCCAGTCC[C/T]AGCTCTGTTCTTTAC	10529
rs529483249	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21039918	ATTAACCATGAAGAA[C/T]GGGAGGATGCAGTAG	10529
rs529492347	snp	A/G	0.00517822	0.0506191	intron-variant	NEBL	GRCh38.p7	10:21007727	TGAACAAACTACACA[A/G]AGAAAGACCCACTAA	10529
rs529500403	snp	C/T	0.0142736	0.0832652	upstream-variant-2KB, intron-variant	C10orf113, NEBL	GRCh38.p7	10:21148468	CCTCAGAAAACAGAA[C/T]CTCTCAGGCAGAGTT	10529
rs529501498	snp	A/G			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20873332	TAAATCTTGTTTTGC[A/G]TAAGGACAGGGAAAA	10529
rs529502449	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21081990	ATGTCAATTACCTTC[A/G]TCAAATGATGAAAGT	10529
rs529515967	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21039318	CCCTATGTCCTGAAT[A/G]GTATTGCCTAGGTTT	10529
rs529521855	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20796883	ATGGCACAAAATCCA[C/T]ATGGTATATGTCTGT	10529
rs529522129	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20982559	TGATTTAGCTGTGTA[C/T]ATTCACTGATTCTAT	10529
rs529537936	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20940742	GACACAATAAAAAAT[G/T]ATAAAGGGGATATCA	10529
rs529548559	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21054419	AAGTCAACCGTTTGC[C/T]CCAAGCATTTCCGGG	10529
rs529557414	in-del	-/TAC			intron-variant	NEBL	GRCh38.p7	10:21153484	ACAGGTGCCCACCAC[-/TAC]ACCTGGCTAATTTTT	10529
rs529563695	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20913831	ATCATATATATGAGA[A/C]AATGAATATTTATGC	10529
rs529565998	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20901642	TGAATTCAACATTTC[C/T]TATTATAAAATATTC	10529
rs529566751	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21045712	TTATCAAAAAGACAA[C/T]ACATGTTGGCAAGGA	10529
rs529575351	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20824905	GCATTTTAAATATTA[A/T]CATTGGAAAGAGAAG	10529
rs529582304	snp	C/T	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21128730	ACTCTCAACTTATCC[C/T]GTAATTGTTAAAACA	10529
rs529583950	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21123755	TCATCTCAAACTAAT[A/G]TATTCATAAAATCTT	10529
rs529584606	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20791549	GCTGGACATACGCCA[C/T]CATGCCCAGCTGATT	10529
rs529592364	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21169367	AAATGTTTCATTTTC[A/T]GGTAGCAGTATACAT	10529
rs529594126	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20860461	AAAACAACCAAAAAG[C/G]GATTATCAACTTATT	10529
rs529597399	in-del	-/CCACTCT	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:21006480	TCTGTGACAATGCCA[-/CCACTCT]CCGTGAGACCTGTAA	10529
rs529610070	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20867292	AGGCTCTTTCACCAA[C/T]AGAATAGTACGTCTT	10529
rs529610452	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20886792	ACTGGGATAAATACA[C/G]GTGAAATGCATAGAA	10529
rs529631110	snp	G/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21104716	TCTGTGTGCTTTTTA[G/T]TACTTTCTCCTGCCT	10529
rs529631434	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21044894	AGGAGAATTGACAAA[A/C]ATACTTAATGAATAA	10529
rs529634145	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21000860	CAAGTGCATTGAAGG[G/T]AGAGAAAAAAGGTAG	10529
rs529635674	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20977617	TTCCACCAAATCCAA[C/T]TGGTACTCAAATCCT	10529
rs529635989	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NEBL, LOC102725112	GRCh38.p7	10:20844178	AAAACCAGTTAAACG[A/G]TATGACCAGTTAGCA	10529
rs529641555	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20893583	GACCTGAAAAACGGA[C/T]ATTTCTCTCTATGGA	10529
rs529641777	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20867622	AGTATATAGAGTCTC[A/C]TGGATTTTCTTTGAA	10529
rs529644839	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20808908	GGGATAGGAAATTGA[C/T]AAGGACAAAGAAAAC	10529
rs529646751	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20803699	TCACTCCACTTTTTA[C/T]AGAGTCAATCAGCAC	10529
rs529652774	snp	G/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21003682	CTGTGAAGCTAAAAG[G/T]TTCTCAGGCAGGATC	10529
rs529660760	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20784753	ATGGAACACCTAAAT[C/T]GCTTATTTACTAGAG	10529
rs529686823	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21061917	TTAGGTTAACATAAG[C/G]TATAGATGCAAGCAC	10529
rs529699568	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21149062	TGGGTTTCCCCACTC[A/G]TCTGTTAGGATTAGA	10529
rs529701319	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21107298	GCTATGATATTGGCT[A/G]TGGGTTTGTCATAAA	10529
rs529709877	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21088078	TGTTTCCCTCCCCTA[C/T]CATTCATGCTACATG	10529
rs529710142	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20804289	TGAGCACTGGACATT[C/T]AATTCAAAATATGTA	10529
rs529713840	snp	G/T			intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20831508	CTTTCTTAGCTCTCT[G/T]GACATCAAGAGTGTC	10529
rs529714349	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21104083	TGAATTAACTTGGTG[C/T]CTTTGTGGAAAATCA	10529
rs529722619	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:20966873	GCAGAAAGCCATCGC[C/G]GATGAAGGAAGAAGG	10529
rs529727049	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21166210	GGGCGACAGAGCGAG[A/G]CTGTGTCTCAAAAAA	10529
rs529731872	snp	A/T	0.0217236	0.101931	intron-variant	NEBL	GRCh38.p7	10:20887421	TCAACCTTTTTTTTT[A/T]TTTTTTTTTTTTTTT	10529
rs529739486	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20941300	CGCAAATCAATAAAC[A/G]TAATCCAGCATAAAC	10529
rs529750054	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21067849	AGCTGGGCATGGTGG[C/T]GAACCTGTGGTTCCA	10529
rs529760543	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20960367	AGAAAAATAAGGCAG[C/T]GATCTTCAGTATTCA	10529
rs529771632	snp	C/T	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20998533	AGAAACCATGGCTCC[C/T]GGCTGCTTCAAGAAA	10529
rs529781942	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20914253	AATTCGGGTGGGTCG[C/T]TATTATTCAACTATA	10529
rs529783355	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21032152	TTTAAGTCTCATGAT[A/G]ACATTAGTGCAACAA	10529
rs529785421	snp	A/G	0.00795532	0.062565	intron-variant	NEBL	GRCh38.p7	10:20943519	GGGTGCAGCACACCA[A/G]CATGGCACATGTATA	10529
rs529799960	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20832372	GTCCTAGATCAAGCC[A/G]TGCCTAGGAATTTCT	10529
rs529811206	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21067299	TTTTAAAGTGAAATA[C/T]ATAAATGCTGGAGAG	10529
rs529811876	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20839514	TACCCTTGGGAAGGA[C/T]TGATTTCCATCACCT	10529
rs529815017	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21084863	ACATGACTTTACCAC[C/T]TGGTCTGGTCATGGT	10529
rs529817457	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20978178	CCCGAAATGAGATTC[A/G]AGTTTATCCAACCAT	10529
rs529818403	snp	A/G	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:20914831	GTAATGGTTCTCAAG[A/G]TGTATTTTTCATATA	10529
rs529821568	snp	A/G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20960886	CAAAATACAGTTCTC[A/G/T]TGAAAAATGGTATGA	10529
rs529845511	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20839027	GGAACCGAACCCATA[C/G]TATCTCCACAGTGTG	10529
rs529848332	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21115105	AGTTTTGTAATAAAC[A/G]TCTTTACATTAATAC	10529
rs529864834	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20826694	AAATTAAATAATCCA[C/T]TCAGATAATCCATGA	10529
rs529871767	in-del	-/T	0.463343	0.130326	intron-variant	NEBL	GRCh38.p7	10:20953507	TAAGACAAGCCCTAA[-/T]TTTTTTTTTTTTTTT	10529
rs529888708	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20799357	TACCAGGTCTCACCA[C/T]GTTGGCCAAGCTGGT	10529
rs529905044	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20793694	AAGTAGCTGGGACTA[C/G]AGGTGCATGCTACCA	10529
rs529916814	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20869422	AGCAAGGTGAGGGGA[A/G]AGATTATATGGGACC	10529
rs529932720	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21017676	GAAGGCATCTATAAC[C/T]ACTAACTGAGCCCAA	10529
rs529934130	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21022465	GGAGTCAGATTCGTG[G/T]TAGGAAAATGTACAT	10529
rs529934712	in-del	-/AAA			intron-variant	NEBL	GRCh38.p7	10:20969480	TACTTAAAAAAAAAA[-/AAA]TGAAATTTTTTTTAT	10529
rs529934811	in-del	-/CACACA	0.00159617	0.0282053	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21128397	CCAGACCAAAAATGT[-/CACACA]CACACACACACCCCC	10529
rs529936392	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20948117	AGTTGAGTGTTGTTC[C/T]TATTTTTAAATTTCT	10529
rs529937405	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21167169	TAAATATTCACGAGA[A/G]GGAATGTGAACACAG	10529
rs529944834	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20793202	TAAGAATACCCAGAC[C/T]TCAATATAAAAATGA	10529
rs529959540	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21036793	CTGAGCATGGACATA[C/T]CCTGTCTTGAGGCCA	10529
rs529964516	in-del	-/A	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20929584	ACTCAGAGAAAGAAT[-/A]AAAATCATATCTCTT	10529
rs529971934	snp	G/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20827310	CTACAGAACACTATA[G/T]AATCACACAGCCTCT	10529
rs529973759	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20787369	CTCGAAATACCCATC[C/T]CAAACCCTCAGAGTG	10529
rs529979044	snp	A/C	1.67764e-05	0.00289619	intron-variant, upstream-variant-2KB	NEBL, NEBL-AS1	GRCh38.p7	10:21173747	AGGTCCAGGCTGGCC[A/C]GGCGCCCCCTCGCTC	10529
rs529979621	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21084918	TGGTGGGGAGTTTAC[A/G]CATGGCTAGCCCTGT	10529
rs529980379	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21078453	CTCCTAAATAGAGTC[A/G]TGTATGTTGTCTATG	10529
rs529988128	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:20900731	ACGCCTGTAATCCCA[G/T]CTACTAGGGAGGCTG	10529
rs529997664	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20937935	GTAGGTAAACAAAGC[A/G]GCCAGGAAGCTTGAA	10529
rs529999682	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:20995782	GCTGTTGCCGAGCCA[C/G]CTCTGCAGATGCTGC	10529
rs530000978	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20942708	GACAAAGGGCTAATA[C/T]CCAGAATCTACAATG	10529
rs530001691	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21016217	AGAGCAGTCCACATC[C/T]ACTGCAGTCAGAGGC	10529
rs530002964	snp	A/T	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:21120758	TTCCCTGTGGAGAAC[A/T]AAGCCCTGCTGAGGA	10529
rs530003172	snp	C/T	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:20903620	CGGAACCAGACTCAC[C/T]GGACATCAACCAATA	10529
rs530005361	snp	A/C/G	0.00199529	0.0315338	intron-variant	NEBL	GRCh38.p7	10:20943140	AAGACACATGCACAC[A/C/G]TATGTTTATTGCGGC	10529
rs530027760	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20862951	CATTATATGTTTTGA[C/T]ACAGGCATGCAGTGC	10529
rs530031823	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20903907	ATCTACGGATTGGGA[A/G]CAATTACACTACTCA	10529
rs530037624	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21042588	AAAATGCCATCAGGA[G/T]GTGCCTTTGCACTGT	10529
rs530044141	snp	C/T			intron-variant, downstream-variant-500B	NEBL, LOC102725112	GRCh38.p7	10:20880297	CCCGGCAGGCAGAGG[C/T]TGCAGTGAGCCAAGA	10529
rs530050061	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20902199	ATGAGGTCAGGAGAT[C/T]GAGATCATCCTGGCT	10529
rs530059229	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20938385	CTGAGGGTCCTGACT[A/G]TTAGAAGGAAAACTA	10529
rs530067694	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20899421	CTCATTTCCCATCAC[A/G]TAATATGTTCTTAGG	10529
rs530077290	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:20810122	CTTTGTAATCAGATT[G/T]AAGTTGCCTGCTCTA	10529
rs530094228	snp	A/C	0.000798403	0.0199641	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20857927	CCCTGACTTGAGAGC[A/C]TGAACTTCAAGTGGC	10529
rs530096825	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20898976	GGTATCACATATCCT[A/G]TTCACCAACAAAATA	10529
rs530097387	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20974327	GGTGCAGTCTTGGCT[C/T]ACTGCAGCCTCAACG	10529
rs530109808	snp	C/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20816820	CTTATTAAGTGCCCC[C/G]AAAATGGTCCTGTCC	10529
rs530115777	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20816330	TTAAAGGTATTCACC[A/G]TAGACTGGTACTACA	10529
rs530118974	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20933785	ACAATAAAGCCTCAC[A/G]GTTTGGTGAATTCAG	10529
rs530124224	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20857502	TGATTATTAAAATAG[G/T]TATGGAAATAACTTA	10529
rs530127201	in-del	-/A	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20906494	TCAAAATAAAATTAT[-/A]ATTAAAGTAAATATA	10529
rs530128262	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21016852	CATTAGGATAGATAC[C/T]TACCCACGTTTTTGC	10529
rs530140889	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20973021	TAAATATATTAGAAG[C/T]GTTGAAGAGTTACAT	10529
rs530142885	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20893261	GGATTCTGAATGCTC[A/T]ATAGAGAGGATAGGT	10529
rs530145724	snp	C/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21060859	CTCAGTCAGCAGCAT[C/G]TGATTCAGTTTATCC	10529
rs530149408	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20788416	ATAAGATTTAATTCT[A/G]AGTGTTATGAATAAT	10529
rs530154488	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20862387	CATTATATAAAAAAA[C/T]GCACGGACCAGACAC	10529
rs530160650	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21103375	CCCGCCACCATGCCC[A/G]GCTAATTTTTTGTAT	10529
rs530165997	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21048071	GCAATGCAAAGTGAG[C/T]GGTTCTCCAAGACAA	10529
rs530184211	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21011420	AAATTTAGTTCCATC[A/G]GTTGCATTGAGTCCA	10529
rs530189526	snp	G/T	1.66034e-05	0.00288122	intron-variant	NEBL	GRCh38.p7	10:20809782	AAACCACATAAATGG[G/T]ATGAACTAAAAAGTG	10529
rs530207399	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20994028	CAACTGCAGCCATCT[A/C]ACAACAGAATCATCT	10529
rs530214232	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20969016	TTTGTTTGGTGCTAA[A/G]CAGGTGCTAAGCATA	10529
rs530217930	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20968510	AGCAAGACCCCATCT[A/C]TAAAATAATTAAATA	10529
rs530224225	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21053915	GTTCGCACCTGTAAT[C/T]CCAGCTACTCAAGAG	10529
rs530230393	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:20835130	GTGTCCATATATGAA[G/T]TTCTGCTCAGAAATT	10529
rs530230877	snp	C/T	0.000798403	0.0199641	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21133964	ACAGTGGCTTACTTA[C/T]GCCTGTAATCCCAGC	10529
rs530231028	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20893867	GATGGGTCCTAAGCT[A/G]TCAGCTACAGGTCAG	10529
rs530240483	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20927753	AGCCAGGGTTCAAAT[C/T]CCAGTTTTGCAGCCC	10529
rs530262044	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21004899	CAGAAAGCATCTCAC[C/T]TTTCTTTTTCCTCTA	10529
rs530265329	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21066215	AAGAATATATGCTTC[G/T]TAAAGCTGTTCAATT	10529
rs530276882	snp	C/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20962419	TTATAAAATAGGCCA[C/T]ACCTAGAGATTAAAA	10529
rs530284937	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20922128	ACAAACACAAAGAAG[C/G]AACAGGGTCAAGAGA	10529
rs530302895	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20978074	GCTCTGGGCTCCTAA[C/T]GCTTCAGGAAATACT	10529
rs530304356	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20883300	TACCTCCAATCCTGT[A/G]GATTTGGTTGGTTAC	10529
rs530319384	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20811127	TTATGGAAATTTCAA[A/T]GGAAAACAGTTCTTC	10529
rs530327244	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20969958	AATTACACAAACTTG[C/T]CTTGGGCCCTGACTC	10529
rs530331356	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20999245	ACAATCATTTATTGA[C/T]TGCCCAATTATGTGT	10529
rs530337038	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20955066	ATTTTAGGAAAACCT[G/T]GCAAGAAACTGTAAG	10529
rs530359953	snp	G/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	C10orf113, NEBL	GRCh38.p7	10:21147263	AAGGTCTCATTGCAC[G/T]TTAGCCATTTTCACC	10529
rs530361935	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21112240	TGATCCCATTACTGG[A/G]TATATACCCAAAGTA	10529
rs530368435	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20915724	TAAACATACATGTGC[A/G]TGTGTCTTTATAGCA	10529
rs530379011	snp	A/G	0.00557542	0.0525036	intron-variant	NEBL	GRCh38.p7	10:20824034	TCAATCAGGCAAATG[A/G]TAATACAAGCATACA	10529
rs530384405	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20840110	TCGTCATCGCTATCA[C/T]CATCATCATTATCAT	10529
rs530384528	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20805802	AGGTTGCAGTGAGCC[A/G]AGATCACGTTACTGC	10529
rs530385548	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20939936	CCAGATTCATAAAGC[A/G]AGTCCTTAGAGACCC	10529
rs530388281	in-del	-/A	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21041687	TAAGAAAATAAAAAT[-/A]AAAAAAATAGCTACT	10529
rs530395016	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	C10orf113, NEBL	GRCh38.p7	10:21148547	TGTTTTTGTTTTTTA[G/T]ACAGAGTCTCACTCT	10529
rs530425640	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21031896	CATTGCACATAAAAG[A/T]TTCTGTCTGTTAGTT	10529
rs530431103	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21113430	CAAGTTCATCAATTA[C/T]GTGAAGAGTTGCTTC	10529
rs530442784	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20794411	AGTATATACTATATC[C/T]TGCTTACTGCTGACC	10529
rs530443964	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20940613	AAGGAAATAGAGACA[C/T]AAAAAACCCTTCAAA	10529
rs530448365	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21019787	TTGTTTTTCCCCACA[G/T]ATGCGGTGTGGAAAA	10529
rs530455700	snp	A/G	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:21030259	CCAGGAACCGGAGAG[A/G]CACCCAAGCTGGCGA	10529
rs530455733	snp	C/T			downstream-variant-500B	NEBL	GRCh38.p7	10:20779941	AATATTCATTTCATA[C/T]TTACGGAATATGAAA	10529
rs530459921	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20999373	AGGGTAAGGTGGGAG[A/G]GTTGCTTGACCCCAG	10529
rs530460240	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20916109	AAACACAATGAATCA[C/T]GAGGTGATTAATCAG	10529
rs530463179	snp	A/C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21065524	TTTCAGAAGAAAGAA[A/C/G]GTGTGAAGGAAGAAA	10529
rs530463462	snp	C/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20874369	CATGATTAATGAAAT[C/T]GGACAGACACGTAAC	10529
rs530466421	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:20950481	TCTGCCTCTTCTCCC[A/T]CATAAACACTTTTAC	10529
rs530473027	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21085334	TTTGTTTTAAAACAG[C/T]ACGTAGGCCAAGTAT	10529
rs530486760	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21019025	GAGCAAGACTCCGTT[C/G]TCCCACCCCTCCCCC	10529
rs530488434	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20801162	TTCCTTTCCCATTTC[C/T]CTACTTGGCTATCTC	10529
rs530488844	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21061112	CCAATACAACTGGTG[C/T]CCTCATAAAAAGGGG	10529
rs530499321	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20945797	CAATGCTCCCAAAAT[C/G]CTGGTGTAGAGGATT	10529
rs530505109	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20935622	AAGCAGAATTAAAAC[A/T]CTGTTACCTCTTTAA	10529
rs530512416	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21088499	TTAAAAAACAAAACA[A/T]AACCTTCTGCCCAGA	10529
rs530519355	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21103503	CAGGCATGAGCCACC[A/G]CACCAGGCCTTTTTC	10529
rs530521408	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20976978	CTAAACAAAGGAACA[C/T]AGCCAACCAAAAACA	10529
rs530525830	snp	C/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20906084	TGAAGAAAGTGTTTC[C/G]AGATTTATGAATCTT	10529
rs530528001	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20902274	AGCTGGGCATGGTGG[C/T]GGGTGCCTGTAGTCC	10529
rs530545317	snp	G/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21036757	ATTTAAGCTTGTCTC[G/T]ACAGAAAGTGAACCA	10529
rs530551108	snp	G/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20930718	GCTTCTACTTAGACA[G/T]GAGCCACATAAATGC	10529
rs530553045	snp	C/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21066926	TCATAGAATACTTAG[C/G]ACACAAAAGATGCTT	10529
rs530558524	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20895605	GTTGTCATTGTCACT[C/T]ATTATTACTGCAATT	10529
rs530558682	in-del	-/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20932589	GAACTTAAAGTAAAA[-/T]TTTTTTTAAAATTTT	10529
rs530561745	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21051181	ATGACCACATCATAC[C/T]CCTTACACAAGAAGC	10529
rs530568681	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:21110595	AACTAGCCCTGGTGT[C/G]ATTCTGTCCTGTACA	10529
rs530594801	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20849241	ACACAAATAAGTCTC[A/G]CTGGAACAGAGAAAA	10529
rs530607500	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21042352	GTGGGCTAGAGTTGG[C/T]TCACACTGGCTCATG	10529
rs530618376	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21160518	AACCCTTAATTATCA[C/T]GTGCCTTAAGCATCT	10529
rs530622273	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20785298	ATTTTCACTAATATT[A/G]GAAATTGCCTCATGA	10529
rs530625895	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21153617	CACTGCAACCTCCAC[C/T]CCGAGGGTTCAAGTG	10529
rs530651501	snp	A/T	1.6507e-05	0.00287284	intron-variant	NEBL	GRCh38.p7	10:20812766	CAAACGCCGTCAGCT[A/T]ACCAACAATGATTCC	10529
rs530652008	snp	A/C	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21126967	GTGACAGAGGGAGAC[A/C]CTGTATCAAAAAAAA	10529
rs530652313	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21119947	ATAACACCTCATTTG[C/T]GGATTTATCTAATTG	10529
rs530653656	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21159806	AGCCTCTCCACTGTC[A/G]CAATTTAATCATCAG	10529
rs530656923	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	NEBL	GRCh38.p7	10:20819198	CAACAGTTACTTTTC[C/T]GGATCCTCTCCCTCC	10529
rs530658050	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20885617	AGCCCTATTTATGCT[A/G]TAAGAAGTTGAGAGC	10529
rs530671590	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NEBL, NEBL-AS1	GRCh38.p7	10:21172994	CGGGATGACTGTCAG[A/G]ATGGCAGCTTGTTCT	10529
rs530680563	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20849743	TGTGGTATTCTGTTA[C/T]AGCAACACAAAATGG	10529
rs530680994	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20842827	AAAAAGTATTCCTCC[C/T]GTTTAGAGATTTTGA	10529
rs530682952	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20802385	AAGATAATTTCAAGT[A/C]ATACTATTCATGAAT	10529
rs530700278	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21090367	AGAAATTCCTTTTCT[A/T]GTCATTATTCCATAA	10529
rs530717940	snp	A/C	0.000798403	0.0199641	intron-variant, downstream-variant-500B	NEBL	GRCh38.p7	10:20813409	CTTTTAATATAATTA[A/C]AAAAACTTATACTTC	10529
rs530749226	snp	C/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21077868	TAGACCTTTCAACAG[C/T]CCGAGCTATGGGCTT	10529
rs530750234	snp	C/T			intron-variant, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20884880	CAGAAGCTTTCTTTG[C/T]AATCTGTGCTTATAA	10529
rs530752428	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20931197	TGTTATCAAAGTATG[A/T]CAAAGACGCACCATA	10529
rs530758807	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20996220	TTCAAGGTTCTCCCA[C/T]GTGAAGTTTTAGGAG	10529
rs530763757	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20974937	ATTGCATGAGTTTGT[A/G]CTTCAGTTCATCTAT	10529
rs530779271	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20965650	GTGGAGGTTTGTATG[C/T]GGAACAGCGGTATGC	10529
rs530779641	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20918305	AGAGATTGCAGTGAG[C/T]TGAGATTGAGCCACT	10529
rs530781138	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20891390	ATGGCAGTATGATAA[A/G]TAGTAGGCTATTTTG	10529
rs530787108	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21112818	GGGGCTTTGAAATTA[C/T]ACCACCCAGTCTTAC	10529
rs530788440	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20862281	TTTATCTTGTTTGAA[C/T]GTTCAGTACAGTGAG	10529
rs530789209	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20924998	CCACCTCTCTTAGAG[C/G]TAAGAGTAATCCTAG	10529
rs530790366	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21043372	AAGCCTGCAATCTTA[A/C]AAAAATCCAAGATCT	10529
rs530790640	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20797067	GCAGGTAGACAGAGA[C/T]GCTATTTCCACTCAT	10529
rs530798164	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21002013	AGGTAGTAATTAAGG[C/T]GATTTGTTAGTTAGT	10529
rs530800025	snp	C/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20883016	CTGTTCCTCCAGACT[C/T]GCAGTATGGATTAAA	10529
rs530806506	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20990008	TCCTGTCACATTAGA[A/G]TTGTTACAGATATCT	10529
rs530813031	in-del	-/A	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20954293	TTCACTCATCAAAGT[-/A]AAAAATAAAAATATT	10529
rs530815601	snp	C/G	0.000798403	0.0199641	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20874261	TTGGAAACAGCTCCC[C/G]CATCACTCCATGTGA	10529
rs530863061	snp	C/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20861847	CCCTTCCTCAACTTA[C/T]GATGGGGTTGCATCT	10529
rs530868977	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20918938	ATGATCATAATAAAG[C/T]GAAACATTATGCATA	10529
rs530871901	snp	G/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20791872	AGAAGAGAATATGAT[G/T]AAGTGTCCTTGGTGT	10529
rs530874354	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20906675	TGTGTCTATGTTCAT[C/T]CAATCATTCACTCAT	10529
rs530877015	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NEBL, NEBL-AS1	GRCh38.p7	10:21172183	TGAAGATGCATAGAC[A/G]TTACCCAACACATTA	10529
rs530879364	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21095389	CAAGGAAAGATGGCC[A/T]GGACCAACTACAGAT	10529
rs530897669	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20837507	TTAAGGAAAGAAGCC[A/G]TCTCCATCATATGAA	10529
rs530905288	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20874854	AAGTAATACTCCTGT[C/T]TTAGCCTCCTGAGTA	10529
rs530910673	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20902126	TTTAATAAGGTGGCC[A/G]GGCGCGGTGGCTCAC	10529
rs530912643	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21066116	GAGAGTGAAGTACAG[A/C]CCTGTGAGTTGGGCC	10529
rs530914125	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20802919	AAATATCTGCTTCTT[G/T]TTCTGCGCCATTCTT	10529
rs530931748	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20786105	TTACTAGTCTAGCAA[A/C]TAGCTTAATATTTTT	10529
rs530938451	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20996934	ATTGATCAATGCCTC[A/G]GCCATTTTGAAAAAT	10529
rs530939224	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20861194	CGTCCCTTAAATATA[C/T]AGTCTTAGAGTCTCA	10529
rs530940670	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21107601	ATTTTTGCATCGATG[C/T]TCATCAAGGATATTG	10529
rs530940999	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20799646	TTCTCTTGCTGAATG[C/T]ACATTCTTTACAGAA	10529
rs530941700	snp	A/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21102104	TCTGCAATGTCAAAC[A/T]TCATTCCTAAGGTCT	10529
rs530941899	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20983635	TCTAATTGTGTACAA[A/G]GCAAAGAGAAATTAA	10529
rs530944724	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21079416	ACACCTGTGTGAGGA[C/T]CTTGTTTTGGAAGTG	10529
rs530952521	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20831041	TCCTATTAATTAGTA[C/T]GGTTAATCAAGTTTG	10529
rs530960894	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20925312	TAATGACTGTGGAAC[A/C]TTCCATGGTATGGAT	10529
rs530970869	snp	A/G	0.000798403	0.0199641	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21140282	AAACAGTGAAAATAT[A/G]AGCGTTTTCAAACAA	10529
rs530973503	snp	C/T			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21141595	GTTTATTTAATGCCA[C/T]CCTTGAACATCAAAA	10529
rs530986258	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21152715	AAGCACAAACTCCAC[G/T]CTGAATTTAAGAACC	10529
rs530987161	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:20838167	TCCTCTGATGAATCT[C/G]GGCAAAGTAAATTGA	10529
rs530988419	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21072467	TGAGAGGTGCCACTT[C/T]TATCAGGAGCCACCA	10529
rs531007389	snp	A/G	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21063541	ATTCACATGTAGCAA[A/G]TCAACAGTGGTTATA	10529
rs531013806	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	C10orf113, NEBL	GRCh38.p7	10:21147230	CTCTGAGCCTGGGAC[C/T]TCCTCCTGCCTCTCA	10529
rs531025911	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20941265	GCTTCATCCCTGGGA[C/T]GCAAGGCCGGTTCAA	10529
rs531027826	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20947007	AGTGAGACATACAAA[A/G]GTCCCCTAAAAAATA	10529
rs531034746	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21014903	AACCACGTTTTCATG[C/T]CTCTGCAGAAACCTG	10529
rs531042237	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20841253	GAAAATTACAAAATC[A/G]AAAGGAGTGATGTAG	10529
rs531045559	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20786613	CCCAAAGAATTTTAG[A/G]GCAATTCAAGTTACC	10529
rs531050871	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21050037	CCTTGAGAGACCAAA[C/T]GAAGGGGGAGGAAGA	10529
rs531056277	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20810348	CAATTGAGAAGTTTA[C/T]GTTTAAAAAACAAAA	10529
rs531059728	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21118467	TTATCACAAGATAAT[A/G]GCACAGTATGTAACT	10529
rs531062786	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20825635	CGCCACTGCACTCCA[A/G]CCTAGGCAACAAAGC	10529
rs531063675	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21070645	AAAAAAAAATTACTC[C/T]GAACATTAAATCTTC	10529
rs531064530	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20868445	GTTCAGATTTATGCC[C/T]GGAGAAAAGAAAACT	10529
rs531064972	snp	A/C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20831370	GATGTTGAAATTTAC[A/C/G]TGTTTGAATCTCAAA	10529
rs531072512	snp	C/T	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:20837681	CATCTAGGACTTCCA[C/T]AGCTAGTGAGGAGAA	10529
rs531079094	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20826220	ATTAAAATGACCTAG[C/T]TCTTCTTCATTGTGA	10529
rs531091030	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20941687	TATCTAGAAAACCCC[A/T]TCGTCTCAGCCCAAA	10529
rs531097989	snp	A/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21008787	ACAACAGTATTTATA[A/T]GGTTCGGTACTATCT	10529
rs531098764	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21071076	GCTTAGGAGGCTAAG[C/T]CAGGAGGATCACTTG	10529
rs531108765	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21076994	CATTTGCACAAAAAT[A/G]TGAATATACATACTG	10529
rs531126281	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21107101	AGACGATGGGTTTTT[C/G]TAAATACACAGTCAT	10529
rs531127343	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21029998	CCCCCGTCCCCCTCA[A/G]AGACCCAAACTGAAT	10529
rs531127771	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21112265	AAAGTATTATAAATC[A/T]TGCTACTACAAAGAC	10529
rs531129803	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20966591	TTTGTGTTTGAAGTC[A/G]TCAGCAATTAGCTCT	10529
rs531132772	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20902594	AAGCCCAAATTAAAA[C/T]GATGTACTCTGCTTA	10529
rs531133874	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20892230	CTGGGGAGCCACACT[C/T]TCTGTGACTTTAGTG	10529
rs531143357	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21152256	CCCCTTGACTTCCAA[C/T]GATCATCAACGAATC	10529
rs531143884	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21165018	ACTTTTAACAATGTG[A/G]CCTTTTCTCTTGTCT	10529
rs531148246	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20861710	ACACAGAGCCCATCA[C/T]ACTGTTTTTGCAAAC	10529
rs531150385	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20820065	TTTATCAAATTGCCA[C/T]TTTATATTTAAAAAT	10529
rs531181059	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20855805	TGGGTTAAAATAAAA[A/G]TAACTCTGATGTTGC	10529
rs531191547	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21112706	TATAACAAACCTGTG[C/T]ATTGTGCACATGTAC	10529
rs531194501	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20840097	GTCACCATCACCATC[A/G]TCATCGCTATCATCA	10529
rs531207597	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21093504	ATCCATCAGTGTTCA[C/T]AAGCTGCTAAGCTTG	10529
rs531234210	snp	A/T	0.000399281	0.0141238	downstream-variant-500B	NEBL	GRCh38.p7	10:20779942	ATATTCATTTCATAC[A/T]TACGGAATATGAAAA	10529
rs531238926	snp	G/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21119098	TAGTTAATTCTGGAT[G/T]ATCTAAATCAATCTC	10529
rs531240277	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20789907	TATATGTATAGATAT[A/G]TGTATATATATATGT	10529
rs531243533	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21153454	GCCTCCTCAGCCTCC[A/T]GAATAGCTGGGATTA	10529
rs531256412	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20973403	TGGGCATGAGCAACC[A/T]TGTCCAGCTAATTTT	10529
rs531257819	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21035113	AAGTGATTATCATGT[C/T]TCAGTCTCCTGAGTA	10529
rs531264700	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20814943	ATGCTGATTCTCAGG[C/G]AAACAGCTATTCAGG	10529
rs531267660	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20794383	TTCTATTCCTATAAT[A/G]TATCCTGTTTATAGT	10529
rs531272007	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20985887	CTTAGAGAATGGGCC[A/T]ACAGGTGAGTTCAGA	10529
rs531275091	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21040573	GAGCGAGAACTCACT[C/T]ATTACCATGGGGAGG	10529
rs531275649	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20993540	GGTTTCAGGGTGGCT[C/T]TATTTCTGCTCCACA	10529
rs531277278	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:20906073	AAAATTCTTAGTGAA[C/G]AAAGTGTTTCCAGAT	10529
rs531283773	snp	C/G			intron-variant, utr-variant-5-prime	NEBL	GRCh38.p7	10:20958140	TACCCACATGAGCTA[C/G]CCCAGTAGCAGCCAC	10529
rs531290707	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20983700	TTGGCCTCATTAATA[C/T]TGGCTAGGCCAACTG	10529
rs531314841	snp	C/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20915600	TCATCATTTTTTATG[C/G]CTGCATAGTATTCCA	10529
rs531316368	snp	A/G			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21126225	ACTACATTGCTGGTT[A/G]TGTTTCAGAACCAAT	10529
rs531320018	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:20954028	ACTCTTCTTAAGGAA[-/A]AAAAAAAAAAAAAAA	10529
rs531321686	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:20823623	TCGTAAATAAAATGA[G/T]TATTTTCTATCCAAA	10529
rs531322688	snp	A/T	0.0119091	0.0762411	intron-variant	NEBL	GRCh38.p7	10:21115954	TTTTAGTCTTCTTTT[A/T]TCATGTTTCATTTTA	10529
rs531330018	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20788818	GAAGAAAAAAGAATG[A/C]AATTCCCATAGATCT	10529
rs531332390	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21100335	TTTCTTTCTTTATTC[C/T]CTCTCGCCACAGTGA	10529
rs531334101	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20986498	TAATTATTGCTCAAG[G/T]TTTGCCAGCCTTCCA	10529
rs531335735	snp	A/C	0.000798403	0.0199641	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20871488	TGACAATGCATTAAT[A/C]CATCAACAGGCTCCC	10529
rs531337714	snp	C/T			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21139180	ATAGCACTAGTGGAA[C/T]TTTTTCTGGGAATCT	10529
rs531337736	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21099135	AAGACCCTGTCTCTA[A/C]AAATAAAAATAAAAT	10529
rs531342862	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20992960	TTTTGTTTTTGTATT[C/T]TTTTAGTAGAGACGG	10529
rs531348120	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20961216	TCCAAAGCAACTACA[C/T]ATATAAATGTTTATT	10529
rs531369642	snp	C/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20858829	TGCCACTTTTCTAAA[C/T]TCCTTTATATGTATT	10529
rs531372475	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20952706	GGACAGGAATTTGAG[A/G]CCAGCCTGGTCAATA	10529
rs531382121	snp	A/T	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21137411	CCTTGGTGTTCATTT[A/T]TAACTCTGAAAAACT	10529
rs531385886	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21106344	TAAGTCTTTAATCCA[A/T]CTTGAATTAATTTTT	10529
rs531404752	snp	A/G	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:20916034	TTTCTACGATAAACC[A/G]TTATTAACTAAGTCA	10529
rs531405776	snp	A/T	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20904597	TTTTGGTTTTGTTTT[A/T]TTTTCAGGTGGGGTC	10529
rs531411058	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20834084	AAAGATAAATGGTCA[C/T]ATATTCACATCCATG	10529
rs531415785	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21149586	ATGAGCCATCGCGCC[C/T]GACCTGTAAGTCTTT	10529
rs531420846	snp	C/T	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21136883	TGGATGGAGGAGTTG[C/T]TTATTGCCCCCAATG	10529
rs531427620	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21010409	GCTACCATGCCCAGC[A/G]AATTTTTTAATTTTT	10529
rs531450988	snp	A/G			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20852893	GACAATTAACCGCAA[A/G]CATAATGTAAAGGAT	10529
rs531465252	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20863926	GGTGTGATGAGGTTG[A/G]AGGAGGGAGTGCTTG	10529
rs531465653	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21105400	GTCCATGTGTTCTCA[C/T]TGTTCAACTTCCACC	10529
rs531485374	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20821974	AAGATCTAACTCCAA[C/T]GTTACCCCTTCCCCA	10529
rs531485891	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20828332	GGAAATTTTGAATTT[G/T]TAATTCCAAAAAAAT	10529
rs531488089	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21011535	GTGAATGAAGGAAGA[A/C]GAAAGCCTGGGACCC	10529
rs531499414	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20824882	TAAACCACAGTACAT[C/T]GATGGGTGCATTTTA	10529
rs531501727	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21067992	AAGAAAAAAAAATGT[A/G]ATATACTTCCCTATG	10529
rs531501728	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21074639	CACACCACCAAGCTC[A/G]GCTAATTTTTTTGTA	10529
rs531503218	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21155535	TGATAACATACAGTG[G/T]TTCTCTTTCTGTGTC	10529
rs531504336	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21150265	TAAACTAAGGATTTA[C/T]ATCGAACGGTTGGAA	10529
rs531508539	in-del	-/A			intron-variant	NEBL	GRCh38.p7	10:21034059	GTAGTCTCAGCTACT[-/A]GGGGGGCTGAGGTGG	10529
rs531511531	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21006702	AGTGGTCCGAGACCC[A/G]AAAAGCATTAGGAGC	10529
rs531530299	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20976152	CCAGCCTAGCCAACA[C/T]GGTGAAACCCCATCT	10529
rs531534259	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	NEBL	GRCh38.p7	10:20817455	CACAATACCAAAGTC[C/T]CCGAAATCTTTCAAA	10529
rs531536747	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21032870	AGGACTCAATTGTAA[C/T]TTCTCTCATGTATTT	10529
rs531537979	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21027210	ATCAAAACTGAGGAT[A/G]TTCTTGGGGACCCCA	10529
rs531543886	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20919121	TTATGTGCTATCCTA[A/C]AAATTCAAAACTAAA	10529
rs531545520	snp	C/T	0.00795532	0.062565	intron-variant	NEBL	GRCh38.p7	10:20909791	TATACAAAAGAAATA[C/T]AGAATTGTCAGAGGA	10529
rs531549028	snp	A/C	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21074215	GTACCATGTCGGTCC[A/C]TGTGCCTCAGCATGA	10529
rs531550025	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20934971	TGGAAATAAACTGGC[A/T]TGCTGTGCAATAGTG	10529
rs531557107	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21017467	CGATCCCACAGATCT[C/T]TGGACATCTCGCCAT	10529
rs531557849	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20894912	CCAGCCTGGGTGATA[C/G]AGCGAGACTCTGTCT	10529
rs531570077	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20782568	CAGATCTGCATCTTC[G/T]TCAAGAAATAAACCC	10529
rs531575238	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:21013312	TTGAAAATAAACATG[C/G]TGAAGCTTCTCCCAA	10529
rs531577000	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21057154	ATGTCCCAGATCTTA[C/T]GCCGGGCTTTCACAT	10529
rs531584647	snp	C/T	0.00438332	0.0466095	intron-variant	NEBL	GRCh38.p7	10:20894301	ATAGTGAGACTCCAT[C/T]TCTACGAAAAAGAAA	10529
rs531589225	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20858568	CCTTTTGTTGTTCAC[A/G]TATTCAGGAAGGGTA	10529
rs531590375	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20811383	AGCAGTTCCACCCTA[A/G]GTGAGATAAATCAGA	10529
rs531591082	snp	C/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21110001	TTCATGCCTCTATCT[C/T]CTTCACTTCTGCTTT	10529
rs531593667	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20969775	GTCTCAAACTCCTGA[C/G]CTCAAGTGATCTGTC	10529
rs531597806	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20812121	CAGAACGCCCATGGC[A/G]TGTCTGTTTTTGATA	10529
rs531598883	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21033155	CCTGTGATTTGTGCC[C/T]AGGAACACCAACCGG	10529
rs531609841	snp	C/T	0.00676609	0.0577691	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21139459	AGAACATAAGGATAT[C/T]AACCCAGGAGACCAA	10529
rs531612156	snp	G/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21006005	CATAGATACGCAAAC[G/T]CAGGCACACACAGAG	10529
rs531622606	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20791636	CCAGTCTCAAGCAAT[C/T]ATCTTGTCTCAGACT	10529
rs531624139	in-del	-/GTT	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21106030	CCACTTTTTGATGGG[-/GTT]GTTTGTTTTTTTTCT	10529
rs531644107	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21122137	TTCAAGCAATTATCC[C/T]GCCTCAGCCTGCCAA	10529
rs531653160	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21109631	ATCCATCTGGTCCTG[A/G]ACTTTTTTTGTTTGG	10529
rs531654925	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21116172	TTTTAATGTCCTTGT[A/G]TTAGCTCAGGCTGCT	10529
rs531656859	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20806415	CAATGTTCTGCCCTA[C/T]CCAATGCATGCGTCT	10529
rs531664555	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20928831	GCTTTTGTAGCTCCT[A/G]TATTTAAAAACAAAG	10529
rs531670760	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21006496	CACTCTCCGTGAGAC[C/T]TGTAAATCCAACCAG	10529
rs531671779	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21059763	TAATTGACTTGAGAA[A/G]GAAAGTGTGGCCATT	10529
rs531686548	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21167719	TGTGTGGCTTGCTGG[A/G]TAGCAAAATGTTTAT	10529
rs531691261	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20889406	AAATAGTTTAAATAC[A/T]TTTAAAATTATTTAT	10529
rs531707500	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20847290	CACTCTCCTCAAGAA[A/G]TGATGGTTGAGCCTA	10529
rs531716509	snp	C/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20878450	CCACTAGTAAATTCT[C/T]TGCAATGAGTTTCAT	10529
rs531725149	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20817846	TATACGCCCACATTC[C/T]GATGGGTCTGATTTA	10529
rs531736950	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20917079	TTAAATTATAACCCT[C/G]CTGATTATGGGAACT	10529
rs531754136	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21000943	GCCCAGATAGAGCTG[A/G]AGAGCTGGTCTCCTG	10529
rs531761546	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20853291	TACTATTTGGACATA[C/T]AGACAAAAAGTTGAA	10529
rs531787138	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20963476	ATTATTTTTGTTACT[C/T]GTCTGTATTTTTTAA	10529
rs531789480	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20801326	CAAGCGATTCTCATG[C/T]CTCAGCCTCCTGAGT	10529
rs531800414	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20943431	AACATCACACACCGC[A/G]GCCTGTGGTGGGTTG	10529
rs531809649	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21000623	AGTGGGTAAGAATTT[A/G]TTTAAATTGAAACTC	10529
rs531834563	snp	A/G	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21142654	GAAAACAGGAGATAG[A/G]CTATATCAGGGGCCC	10529
rs531849219	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20807882	ATTGAAGTTCTAGGC[C/T]TAATCCATCAGCCTG	10529
rs531850175	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21043314	TACAAAAAAACAGCC[A/G]TCAACATTGACGAAT	10529
rs531860561	snp	A/C/G	0.00199529	0.0315338	intron-variant	NEBL	GRCh38.p7	10:20829220	AAACTACTTAAGAAA[A/C/G]TGTGGCACATATACA	10529
rs531870554	snp	A/T	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21141880	GTTCTACCCATAGGG[A/T]GCCTGAGGTCCAGGA	10529
rs531874050	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20994423	TATACATTAATTCAA[C/G]CCTCAAAAATCACTG	10529
rs531893736	snp	C/T	0.000798403	0.0199641	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21128074	AGGAAGTTAATGACT[C/T]GGTTGGGACTAGAAT	10529
rs531905597	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20944973	GTTGACCACAGGACT[A/T]GATTAAGCACTCTCA	10529
rs531910521	snp	A/G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21167484	ATGTTAAACTATTGC[A/G/T]TCGTTCCTTGGTGGC	10529
rs531915205	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20956740	AATGTATTTCAATGA[A/G]TGACTTTATAATTTT	10529
rs531915513	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21061369	AATATATGGGTCAGA[C/T]TTATGTTTTATATCA	10529
rs531918609	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20910884	GCTAAAGAGTAGGCA[C/T]TGGCCAGGCATGGTG	10529
rs531920198	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20829535	AGCACATGTATACAT[A/G]TGTAACTAACCTGCA	10529
rs531920362	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21025823	AGTAGCACAATTCAG[C/G]CTTGCTGCAAAATTC	10529
rs531934402	snp	A/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21014886	TTATCGTACTTCCTA[A/T]GAACCACGTTTTCAT	10529
rs531938434	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:20975533	TATAGGGATTGTGTA[G/T]GTTTCATTTCTTTAA	10529
rs531941052	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21103995	TGCTCAGGTTTTGTT[G/T]TGTTTTCTTTTCATG	10529
rs531944118	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21091085	ACCTCTCTCGGATTC[A/G]TCTGTGTATTTCCTT	10529
rs531944555	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21098223	ACACATTCTCACTCA[C/T]ACGTGCACACATACG	10529
rs531984619	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20796273	GAGGCTGAGGAGAAT[C/T]GCTTGAACCCAGGAG	10529
rs531986595	in-del	-/TGTATA	0.00279385	0.0372709	intron-variant	NEBL	GRCh38.p7	10:21123827	CCAATTGGTTGTATA[-/TGTATA]TGTATATGTATATCT	10529
rs531993049	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21008704	AATGTAAACTAGTTA[C/T]TGTTGTTAATCTCTT	10529
rs532002554	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20790496	ATCCCAGCTACTCGG[A/G]AGGCTGAGGTAGGAG	10529
rs532011366	snp	C/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20988440	CCCACCAAAAAAAAA[C/T]TGACCAACCCTCTGC	10529
rs532034013	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20850065	GTTTTTATGAACTCA[C/T]CATAGTTTTACATTA	10529
rs532035770	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21121908	ACTTTGAAAGCAAAA[C/T]GCTATCAAAATTTGA	10529
rs532035997	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20872748	CCAAGATGGCGACGA[C/G]AGTGACCTCTGGTCA	10529
rs532047367	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:20832053	TCCTAAACCATCCAG[C/G]TTCGGTGAGACTGGC	10529
rs532048181	snp	A/G			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21126773	GGGTCAGGACTTTGA[A/G]ACCACCCTGACCAAC	10529
rs532053727	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:20946671	TTCACCACGCTGTTG[G/T]CCAGGCTGGTCTCAA	10529
rs532057083	snp	A/G			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21137206	AGTGGAGATAATTAG[A/G]ATATTTGTCTCAAAG	10529
rs532062313	snp	A/G	0.00398564	0.0444627	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20960429	AACTAAGAGACAAAT[A/G]TCATGAAGTCTTAAA	10529
rs532089328	snp	G/T	0.000798403	0.0199641	intron-variant, utr-variant-5-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20897458	AAAATTTGATTTTAT[G/T]AACTTTTAAAGTCAA	10529
rs532090355	snp	A/G	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:20974995	CAAGTTTCATGATTC[A/G]ATATAATTCCATGGT	10529
rs532092443	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21106620	GAAGTCAGGTAGCAC[A/G]ATGCCTCCCACTTTG	10529
rs532101067	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20961552	TGGCATAGTCTATGC[A/G]TGCACTGAGTACTGC	10529
rs532103517	snp	C/T			utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20784449	CTGTACTAAAAAATC[C/T]CTGATGACATTCCTG	10529
rs532109192	snp	C/T			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21129474	AAACAATGTATTCAA[C/T]TATATATGCTTATAT	10529
rs532109686	in-del	-/A	0.169435	0.236663	intron-variant	NEBL	GRCh38.p7	10:20828080	CTTAAAATAAAAGTT[-/A]AAAAAAAAAAGTGCT	10529
rs532112677	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20881990	AGAGAGACTTGCTCA[C/T]GACAAAGTGAGGCTC	10529
rs532113174	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21061995	CCTGAAATTTCCTAC[G/T]GCCCAACACGCACAA	10529
rs532119988	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:20802232	GATACACATTGCAGG[C/G]AATGAACTAGAGGCA	10529
rs532121908	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20972684	CCCGGGAGGCAGAGG[A/C]TGCAGTGAGCCAAGA	10529
rs532123526	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20926374	CTAAGAGGGCTTAAA[C/G]AAACTTGTGATTTGA	10529
rs532124664	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21056656	CATGTCAAAAGAACT[C/T]GATATATTCTACATT	10529
rs532136698	snp	C/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20931937	ATTTTATTACTAACA[C/G]CATATTCTTTCATGT	10529
rs532143636	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21026534	CTTAATCTTTTGCCA[C/T]ATTCTAAATCGATTA	10529
rs532151711	snp	A/C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20997277	CTCCCTGCCCTCTCA[A/C/G]TCTCTGACCACAGCC	10529
rs532164433	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21084453	AATGTTAAAACTAAG[A/T]CTCAGCCTGTAATCC	10529
rs532175404	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21062430	CTTTGGGAGGCGGAG[A/G]TGGGAGAATTACTTG	10529
rs532186043	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21056114	GACACTAGGTCAGAT[A/G]TCTCTGCATCATGAT	10529
rs532190335	snp	A/C	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21143213	CAGCACTTTAGGAGG[A/C]CAAGGTGGGCGGATC	10529
rs532192423	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NEBL, LOC102725112	GRCh38.p7	10:20844945	TTCAAAACATTTTTT[A/T]AAAAACTGCTATAAA	10529
rs532194143	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20966411	TGCAATATGCTACAC[A/G]TTAAATGAATGTTTG	10529
rs532197658	snp	C/T	3.30699e-05	0.00406618	intron-variant	NEBL	GRCh38.p7	10:20808481	AAAAAATGAATCGAT[C/T]TTCTTTGTAAGCAGT	10529
rs532203744	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21109598	CCTCTTTGTATCTTT[C/G]GTAGAATTCGGCTGT	10529
rs532206514	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21027177	TATGCTGATTCTTGT[A/G]AAACCTCCCAGAGAA	10529
rs532211864	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20875071	GCCAAATCTGTTCTT[C/T]GTTGCTTCCAACGAA	10529
rs532218472	in-del	-/C	0.00835141	0.0640778	intron-variant	NEBL	GRCh38.p7	10:20904466	CAAGTGATTTGATTA[-/C]CCTCATTTCTTTAAC	10529
rs532228023	snp	A/G	0.000798403	0.0199641	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21142715	AGCATTACTGCTACT[A/G]CCTTCTGAGATCAGC	10529
rs532239599	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21068611	TGACACCTGACCATA[C/G]ACCCCGGACCCATGG	10529
rs532251310	snp	C/T	1.71864e-05	0.00293137	intron-variant	NEBL	GRCh38.p7	10:20831601	GCAGAAAATGAAACA[C/T]ACAGTTAGTGCTCTC	10529
rs532255082	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20804113	ACAAAACAGCCAGTA[C/T]CTCTGATCTTGTTGG	10529
rs532256427	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20967182	TGTTTCTATTTTCAA[A/T]GAAAAAAAAAAATAG	10529
rs532265120	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21115600	TTGCATTGTTTCCAA[C/T]AAGGAGTTCGCTCAA	10529
rs532268983	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20829095	AGCAGATACTATTAT[C/T]ATTTCCATCTTACAG	10529
rs532281071	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NEBL, LOC102725112	GRCh38.p7	10:20844132	ATTTCAGCACATTAC[A/G]TATTACAACACTGAA	10529
rs532291521	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:20935956	ATCTAAAACTGTAAG[C/G]GATGGTAATCAAAAT	10529
rs532307898	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21155444	TCCCACTAACCTTCC[C/T]AGCTTCTGGTAACCA	10529
rs532310295	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20803538	CAACAACATCCAGAA[A/G]AAAAATAGCGTTTCT	10529
rs532313436	snp	A/G	0.00119737	0.0244387	intron-variant, downstream-variant-500B	NEBL, LOC102725112	GRCh38.p7	10:20880535	AATGCTTGATAACCC[A/G]ATAGGTCTGAAGGAT	10529
rs532313872	snp	A/T	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:20832140	CTGATTTGCCACTGG[A/T]CAAGTCAATGTTCCC	10529
rs532327864	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20942196	TCAAACTATACTAAA[A/T]GGCTACAGTAACCAA	10529
rs532334070	in-del	-/T	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:20906471	TAACTTAAACTATAA[-/T]GATAATATCAAAATA	10529
rs532341127	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21162821	ATCTTCACAAAGGTA[A/G]GCATAGCCTTACAGA	10529
rs532344372	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21032747	GTTACAGAATCCAAA[A/C]CCCTGGCTCTCTAAA	10529
rs532352691	in-del	-/GAGATCTAAGGTACT	0.00557542	0.0525036	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20870675	AAGGCCCATGCCTAG[-/GAGATCTAAGGTACT]GAGAGCTTTATCACC	10529
rs532365204	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20953118	GTATGGACTGAACTG[C/T]GTACCACCCCAAAAT	10529
rs532366806	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20832621	GTTATTAAAAAAAAC[C/T]ATTAACTATAGCCAA	10529
rs532380644	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20862291	TTGAACGTTCAGTAC[A/C]GTGAGTGATTTGATT	10529
rs532385026	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	NEBL, NEBL-AS1	GRCh38.p7	10:21174660	CCCAGGCCCAAGGGC[A/C]GGGAGATCCGCGGGG	10529
rs532388290	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21043296	ACCAACCAGTTGTCA[C/T]CCTACAAAAAAACAG	10529
rs532393181	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21167254	TTCGGAAACCATGTT[A/C]AGTGAAACTCTTTGA	10529
rs532409930	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21032272	TACATATTGGGGTCA[A/G]TCTGGGCATTTTCCA	10529
rs532410290	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20914204	AGCTGTGGATAATTC[A/G]ATGTCAGTAAGTGCT	10529
rs532418613	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20937625	TGCACCAAGCGTGAG[C/T]TGAAGCAGGGTGAGG	10529
rs532419130	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20875446	GCCAATAAGAGAAAT[C/G]CATATGAGATTTTGA	10529
rs532421323	snp	A/C	0.000113216	0.00752298	utr-variant-5-prime, upstream-variant-2KB	NEBL, NEBL-AS1	GRCh38.p7	10:21173861	CGGGGGCGGCGGCGG[A/C]GGCGGCTGCTGGCTC	10529
rs532426363	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20919431	TTTCTATAATCATGG[A/G]AATCATGTCATGGTG	10529
rs532432053	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21073577	AGCCTAGAATGCACC[A/G]GTACACTCTAGCCTG	10529
rs532434622	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:20969388	ACTGCATTCCCAGAG[C/G]CTCTTAGTGATATTT	10529
rs532451535	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20937901	TGGAGGAGGGGCGCC[C/T]GCCATTGCCCAGGCT	10529
rs532460229	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21043789	TAATAATCATGTTAT[A/G]TTTATTCAACATAGA	10529
rs532475820	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21165196	AATTATTTTCCCATT[A/G]TACAGATTACAATTT	10529
rs532477888	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21055434	GATCTTTTAACTTTG[A/G]TGTCAATGCTGTATT	10529
rs532491676	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20826625	AGACAATTTCTCAGG[C/T]TTTATAATAATATGA	10529
rs532494142	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21085943	CTTTTATGGAAATCT[C/G]CATTTTTTTCATTTG	10529
rs532503959	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20857434	AATCTATGCCTGGCC[C/G]AAAGCAGATATTCAA	10529
rs532509586	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21017522	ATTATTTGTATATGC[C/T]ACCCTTTGAAGCTTG	10529
rs532509877	snp	C/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	NEBL, NEBL-AS1	GRCh38.p7	10:21173132	CATCTCCGTCCCTGC[C/T]CGGGAAGGGCAGGGG	10529
rs532514826	snp	G/T	0.0023933	0.0345097	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21134958	CACACACTTAATATT[G/T]TATGCCTTTTTAAAA	10529
rs532521512	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20808143	GATTTTTTTCCTTAA[C/T]GGAAATCATATAAAA	10529
rs532528796	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20820974	TCCTCTGGCCTCTTT[A/C]CTCGATATGTAACTT	10529
rs532532394	snp	A/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20882245	AGGAAGGAAGGAAGG[A/T]AAAGGAAAAGAGAGG	10529
rs532541605	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20985213	CTTCCACAAAATTGG[A/T]CCCTGGTGCCAAAAA	10529
rs532541686	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21001777	CAACCTCAGACATGA[A/G]TGGATTAATTGCCAT	10529
rs532543921	snp	G/T	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21128417	CACACACCCCCAAGA[G/T]CATTTCAAATACTCA	10529
rs532550560	snp	C/T	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21141713	ACAAAAGGGAAAATT[C/T]CCATTCTTAATAAAA	10529
rs532550592	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:20972890	TTTCCTTACTGCTGA[A/T]TTTCATTTAAAATAT	10529
rs532557484	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20820591	AACAGTTTGGAAGGC[C/T]GAGGCAGGTGGATCA	10529
rs532565487	snp	A/G	0.00126955	0.0251628	NEBL	10	allele_origin=G(germline)/A(germline)	10:20787250	TGACACACTGGTCTG[A/G]TGCATGTAGCCATAG	10529
rs532565514	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21022436	AAATAAAGATTAAAT[A/G]TTGTAGCTCCCACGG	10529
rs532572566	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20992966	TTTTGTATTTTTTTA[A/G]TAGAGACGGGGTTTC	10529
rs532582772	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20898460	AAAAAAAAATGCCTT[A/G]GCCTTACCTAAACTG	10529
rs532584375	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20903556	TTATATCAAAAAGAC[A/G]TCTGCATGTGTTATG	10529
rs532590312	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20979832	CTACCTCAGCCTCCT[A/G]AGTAGCTGGGACTAC	10529
rs532608186	snp	A/G	0.00159617	0.0282053	upstream-variant-2KB, intron-variant	C10orf113, NEBL	GRCh38.p7	10:21148371	TGTGGACTTTGGTCC[A/G]TGGTTCCCAAAGCAG	10529
rs532613316	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20947794	CTGAGCACATGCTTC[A/C]TGCGTAAGTGAGGTA	10529
rs532616581	in-del	-/T	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:20925844	CGACATTTTGGGCAG[-/T]TTTTTTGTTTCCTCT	10529
rs532617716	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20961230	ATATATAAATGTTTA[C/T]TTCAAAAGTAAGATG	10529
rs532628064	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20780808	GCAGGGAACACATTA[A/G]AGCCATTGCTGACAC	10529
rs532644108	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	C10orf113, NEBL	GRCh38.p7	10:21148128	ACAGTTGAGGCCTAA[A/G]GGACAAAAAGTCATC	10529
rs532653706	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20927732	CACAGCCTGTGGCAG[C/T]CAGACAGCCAGGGTT	10529
rs532667000	snp	A/G	0.00279162	0.0372561	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20780571	CGGGGTATTATTAGG[A/G]TGCATTGCTTGCATC	10529
rs532670662	snp	A/G	0.000798403	0.0199641	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21127197	AATTCATTATTCAGA[A/G]AATGGATCAATAACA	10529
rs532671366	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21154101	TCAGAAAGGAACTTC[C/T]CATATTATTAATACC	10529
rs532675610	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20961820	TGAACAGAGGGATCA[C/T]GAATCCCACTCGGGA	10529
rs532678730	snp	A/T	1.65132e-05	0.00287339	intron-variant, missense, utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20815662	TTCTTCACTCTTTCC[A/T]TTTCAGGAGTTACAC	10529
rs532682256	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20933251	AGTAAATTTATAAAT[A/T]GTTACCTGTGACCAT	10529
rs532684126	snp	C/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21090481	TGCGTGTAGGTTATA[C/T]GAAAACACTTTGCCA	10529
rs532694338	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20946407	GTTTTTCAAATATTC[A/C]ATTTCTTGAGCCAGG	10529
rs532699776	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21066886	ACACTTAAGAACTTT[C/T]AGCATCATGTTCAGT	10529
rs532702577	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21097563	CTTAAATGAGTCATT[C/T]TGTATATTGCCAGGC	10529
rs532704832	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21010048	CGAGACAGTAGTGTC[C/T]AAGTAGTGTCCTCCT	10529
rs532709597	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21112051	TGAGATACCATCTCA[C/T]GCCAGTTAGAATGGC	10529
rs532741452	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20816254	GGCATACCATCCGTA[A/T]AGCTGTAATAAATAT	10529
rs532761462	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20872165	CAGCCTAATGACTGC[A/G]TGAAGAGAGGTGAAC	10529
rs532762593	snp	A/G			intron-variant, upstream-variant-2KB	NEBL, LOC102725112	GRCh38.p7	10:20845057	GGGTAATTTCTTCTC[A/G]CAACTTTAATGGGAA	10529
rs532767194	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21004260	TCTAAAATGCAGACA[C/T]CGTTATGAATAAATG	10529
rs532778947	snp	C/G			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21137991	GAAAGGAAGGAACTG[C/G]AAGTGGATGGAGAGG	10529
rs532782500	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20944899	TCAACAGTCAGACAT[A/T]AGAGGCCACAAGATC	10529
rs532782627	snp	A/C	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21140922	AGGTAACAAACCTGC[A/C]TGTTCTGCACATGTT	10529
rs532785903	snp	G/T	1.72027e-05	0.00293275	utr-variant-3-prime, intron-variant	C10orf113, NEBL	GRCh38.p7	10:21125822	AGTGTCCTTCAGACA[G/T]TTACAAAAAAGTCAT	10529
rs532786377	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21164291	ATTTCTCCTTCCTCT[A/G]GAGACTTAAAGGAGT	10529
rs532786848	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20888029	ACGTTTTATTAAAAC[A/G]CTAAGTAGCTTTTTT	10529
rs532806661	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21022152	AGACACCTTTAGCTG[C/T]TGTGACCCCATGGTC	10529
rs532807680	snp	C/T	1.66424e-05	0.0028846	intron-variant, synonymous-codon, nc-transcript-variant	NEBL	GRCh38.p7	10:20823277	AATGGCTGTTGCATG[C/T]TTAATCTCTTCTTTG	10529
rs532808334	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20899748	TGTTATGCCAGGCAC[C/T]GTGCTTGGTGTTAGA	10529
rs532817542	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20790208	ATTATTCTCATTTGC[C/T]ATCTGGCTGAATTAG	10529
rs532818193	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21170602	GGAAGCACGGTGTAG[A/G]AGGATCGAAGACATC	10529
rs532819295	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20810338	TCATAGGAAACAATT[A/G]AGAAGTTTATGTTTA	10529
rs532831296	snp	A/C	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:21004701	CTCCAGCCTGGGGCA[A/C]AAAGCGAGACTCATC	10529
rs532851222	snp	A/G/T			intron-variant	NEBL	GRCh38.p7	10:20805618	GGCATTTTGGGAGGC[A/G/T]GAGGCAAGTGGAGCA	10529
rs532856108	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20839632	AGGTCATGTTTTAAA[C/T]ACATAAAAATTTAGA	10529
rs532862692	in-del	-/C	0.00517822	0.0506191	intron-variant	NEBL	GRCh38.p7	10:21002786	CAAGGGGGAAATCTG[-/C]CCCCATGATTCAATC	10529
rs532879627	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21052861	TCACCTAGTCCTACT[C/G]ATGACTCCACTAAAG	10529
rs532895688	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20859654	TACAACACAGTCGAT[C/T]CTAAAAAAAACAAGA	10529
rs532897992	snp	C/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20867606	TCTGTTATCCTTATG[C/T]AGTATATAGAGTCTC	10529
rs532906798	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21024920	GTCAAGCATCTAACA[C/T]GAATCGGTAGCACCA	10529
rs532920120	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21028457	GTAAATGTGCACACA[C/T]GCATGCACAGGCACA	10529
rs532924986	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20935307	AATAACAGAAATTTT[G/T]AATCTTCTCAAGACT	10529
rs532930783	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21088259	TAGTTCCAACACTTT[G/T]GGAGGCTGAGACAGG	10529
rs532932025	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21040537	ACTCCTTTAAACAGC[C/T]AGCTCTCATGTGAAC	10529
rs532937263	snp	A/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20970590	TGAGGTGAAGGCTGC[A/T]GTGAGCTGTGATCAT	10529
rs532940746	snp	A/C	0.000798403	0.0199641	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21131110	AAGAATACTACAAAC[A/C]ACCCTATGCTCACAC	10529
rs532951670	snp	A/G	0.00557542	0.0525036	intron-variant	NEBL	GRCh38.p7	10:21082908	GCTGGGATTACAGGC[A/G]CCTGCCACCACACCT	10529
rs532954044	snp	G/T	0.00597247	0.0543191	intron-variant	NEBL	GRCh38.p7	10:20905108	CAAAGGAAAGGGTTT[G/T]GGGGGTTGTAGAGCA	10529
rs532959870	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20829473	GATAGCATTAGGAGA[C/T]ATACCTAATGCTAGA	10529
rs532966689	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20793552	TATTTTTCTTTCTTT[A/C]TTTTCTTTTTTTTTT	10529
rs532984454	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21004539	CCCTGGCTAACACAG[C/T]GAAACCCCATCTCTA	10529
rs532996302	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21046245	TGAGAGGAATAGGGA[A/G]ATGTTGGTTGATGGG	10529
rs532999907	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20964780	CAATAATGAAGTCAA[C/T]ACAGAGGCAAGCAAA	10529
rs533000579	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20854046	AACAATTATAAATTA[G/T]AAAATTTTAAAAATA	10529
rs533002906	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21057931	TCCGAATTTCATCAG[C/T]AAATCATATAATCGT	10529
rs533018076	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21150234	AGCCTCATTTATGTG[C/T]GGCTTGCATCTTTTT	10529
rs533033302	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21088683	GGCATCAGATGCACA[C/T]ATTAGCAGCAAAGAA	10529
rs533036440	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20848663	GTGCACTCCTTATGA[C/G]AATCTAACTAAAGCC	10529
rs533037168	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20790914	TGTCAGGTTCATTTG[G/T]CAACAAACAAGGGCT	10529
rs533044776	snp	C/G	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21144875	TGGTTAGCATGGGCT[C/G]TCTCCTCTCAATGAA	10529
rs533049392	snp	A/G	0.0130921	0.0798413	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20784393	TATTCGAAAATCAAA[A/G]CATGGCAACAATTTC	10529
rs533050366	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21018910	GCAGGCGCCTGTAAT[C/T]CCAGCTATTGGGGAG	10529
rs533059437	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20965145	TTTACTGAGCACCTA[C/T]TATGGGCCAAGAGCT	10529
rs533069927	snp	A/G	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21131888	GCTGTTGTATTTTTT[A/G]AATGGTCAATGCTAA	10529
rs533087215	snp	C/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21065637	CACATCCACCTCTAG[C/G]ATCTTCACACAAAGC	10529
rs533098709	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20981667	CATGGACATGATATC[C/T]AGTCAGGGCCAGAGA	10529
rs533113615	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20885476	GTGGTGTCTATTTCA[A/G]TATAGGATAACATGC	10529
rs533114614	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21012910	GGCCTTGGGAAACAG[A/G]TGAAAAGGATGCAGG	10529
rs533131799	snp	C/T	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:21151100	AGGAACTGAAGTCAT[C/T]TTTGGAGAAATAAAC	10529
rs533134626	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:20823074	ATGTGTAAAATGCTA[G/T]CTCCACTTTTAAGGA	10529
rs533141190	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21063305	AGAGATCATTCCATG[A/G]TCACCATCAAGGACA	10529
rs533150530	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21054587	AATAAGTTTTTCTAA[A/G]CCATTTTCAATTCAT	10529
rs533154076	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20935567	AGGATACTGTGCAAT[A/G]AGAGACTGATTCTGG	10529
rs533155206	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21027904	AAAAATGGTTGTTTT[A/T]TGTCATTCAAAATTA	10529
rs533155242	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21034387	CTTATGGGCTACCTC[C/G]TGTGCTCAGAGCAGA	10529
rs533157259	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20995602	GATAAATAGGAGGAC[A/G]CTGGAGAAACGAAAT	10529
rs533157352	snp	C/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20916752	TTAAAAGCTTCTAAC[C/G]TGGCTTAGGTATAAA	10529
rs533158346	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20818444	CCAGCACAGAGTAGC[A/G]CTGCCTTGTTAACTA	10529
rs533160870	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20918258	AGCTACTCAGGAGGC[G/T]GAGGCAGGAGAATCG	10529
rs533167577	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21150442	TGATGGCTGGGAGTC[C/T]ACCCAGTGAGGCTCC	10529
rs533168612	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21101312	TCGATTCTCAGTTCT[C/T]CCAAGGTAAGACTTC	10529
rs533170107	snp	A/G	0.00517822	0.0506191	intron-variant	NEBL	GRCh38.p7	10:21006559	CAGCCACTCCTGCTA[A/G]AGCTTGAGACTTTCT	10529
rs533170224	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20956662	AAAATCAGAAGCTTT[C/T]ACATAAATGTTTCAT	10529
rs533173015	snp	A/C	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21094240	GGAGACGGTGGCTCA[A/C]GCCTGTAATCCCAGC	10529
rs533197478	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20879583	CAGTTGCCGTTCTGC[A/G]GAAAACACTCTGCAC	10529
rs533200010	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20796650	TTTAGAATTTCTGCT[A/G]TTTTACTTCAGAATA	10529
rs533211430	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21117482	TTAGGGTAATTCCTG[G/T]GCTCTGTTATATGTC	10529
rs533212762	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21101309	GTATCGATTCTCAGT[C/T]CTTCCAAGGTAAGAC	10529
rs533215556	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20796955	GAAAGAAAAGAAAGG[A/C]ATGTACAGTGCAGAC	10529
rs533223305	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20930701	TTGAGCCTAAATAGA[C/T]GGCTTCTACTTAGAC	10529
rs533223351	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20923565	AAGCCTGTAGTCCCA[G/T]CTACTCAGGAGGCTG	10529
rs533225203	snp	C/T	1.64866e-05	0.00287106	intron-variant, synonymous-codon, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20868664	TCACTAAAGCCTTAC[C/T]TGACTAGAAAGTTTA	10529
rs533232889	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20936480	ATTCAGTCTGCTTGT[C/T]ACTCTGGCCCATGTC	10529
rs533242291	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20912167	AAAATAAACTAGATA[A/G]CCAACACAACTATTT	10529
rs533252362	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20873379	CAGCAGAGATGTGAA[C/T]TTGAGGGCCAATAAT	10529
rs533259986	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21063801	CGTGAACCCGGGAGG[C/T]GGAGCTTGTAGTGAG	10529
rs533261201	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20886803	TACACGTGAAATGCA[C/T]AGAACAACTTCTGTG	10529
rs533275544	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20890861	ACTGGGAAGGCAAAA[C/T]TATGACTCATTGAGA	10529
rs533299253	snp	G/T			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21144651	GAATCACTTGAACCC[G/T]GGGAGTTGGAGGTTG	10529
rs533300011	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21163032	AATCCTTAATCCTAA[A/G]AGATAGAGTCTATTA	10529
rs533304629	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20849160	CAAAACTTTGATATA[A/G]GCTGCAGACAAAACC	10529
rs533306141	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20830246	AAATTTCACCAAATG[C/T]TGTTACACAATCCTT	10529
rs533311872	snp	G/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20842229	CTGTTTTATAATTTT[G/T]GAATGATCTGAGTCA	10529
rs533320574	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20824976	ACCAGGCTAACACAG[C/G]CTCTCACCATGAAAG	10529
rs533343243	snp	C/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21123497	AGTCTTTTATGTCAC[C/G]AGAGCCCTGAGCTCA	10529
rs533345107	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20807277	GCTGCAGTGAGCTGA[C/G]ATTGTGCCACTGCAC	10529
rs533345377	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20906608	GGTGATTTCTCTCTG[A/G]GGACTTTATCTTCTT	10529
rs533348005	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20842689	AATAATTAAATCAAT[A/C]TAAATAATATATCCA	10529
rs533352665	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21038764	ATGGGATTTCTGGCT[C/T]TAGATCCTTGAGAAA	10529
rs533366621	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21001916	TCTCTGTTTTTCCAC[C/T]AACACTTATTTCTCA	10529
rs533382076	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21096848	TTTTGGCTAGTTTCA[C/T]CACATTGGTCTTTCT	10529
rs533386520	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20785623	TACCTGTGTGTCTAA[C/T]TGTCAAAGGAAGGAT	10529
rs533390874	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20958633	ATTTCATGGGGAAAA[A/T]AATAATTTTGCTTTA	10529
rs533401623	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21055719	TGTGTTAGATAAACT[A/G]CAATTTACACAACTC	10529
rs533414959	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20802218	AATACCGGGAAGCAG[A/T]TACACATTGCAGGCA	10529
rs533432113	snp	A/G			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20873816	CACTGAATCTATAAA[A/G]TGCCTTAAAGAAAAA	10529
rs533436843	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21014217	CAACCTCAAATTCCT[A/G]GGCTCAAGTGATCCT	10529
rs533438328	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20936409	AACAGGCTATTGCAA[A/G]TGGAACCTAAAAAAT	10529
rs533455694	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20952029	TCCACATTCTGAACT[A/T]CATAATTCAACCAAG	10529
rs533458919	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21156392	GGAAAAGAGAGCAGT[A/G]TGTTTGGGATTCGTT	10529
rs533463927	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21163396	GCCATCAAAAATACA[C/T]CTACTTATAGGGCAC	10529
rs533473966	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20819696	TTGGCGATGCCAGTC[C/T]TTTCCTTGTCAAGTG	10529
rs533489238	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21080202	GATTTCTTAACAGCA[C/T]AACACATAGATACAA	10529
rs533490476	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21039187	GGTTGCCTGTTCACT[C/T]TGATGATAGTTTCTT	10529
rs533507807	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20837373	CCAGACACAACATCC[C/G]CTTAAACCAAACCTA	10529
rs533510807	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21069072	TTTTATATTTTTTGT[A/G]GAGACAGTGTCTCAC	10529
rs533513048	in-del	-/A	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20886622	GCATAGTGTGTGGTT[-/A]AAAAACCTAGACTCT	10529
rs533524115	snp	G/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21081118	CCTCGACCTCCCAAA[G/T]TGCTGGGAATACAGG	10529
rs533530848	snp	A/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20907462	TATATGACTGAATAA[A/T]AAACATTCGATAATT	10529
rs533539726	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20914331	CATAGAAACCTTAAA[A/C]GATACAGTGAACAAG	10529
rs533551998	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21123146	CTATCCCTTTGAGGT[A/T]GATACCAAAGGATGT	10529
rs533555516	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21044818	CACTCAGGATAATCC[A/T]TCATGACATTTGTGT	10529
rs533564504	snp	G/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20854124	GCCTTATTTGGAAAA[G/T]ACCTTTAGTAGTAAA	10529
rs533575639	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20933245	TTTTATAGTAAATTT[A/G]TAAATTGTTACCTGT	10529
rs533580369	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20867745	TCTTCCCATGACAGA[C/T]GGTGTGTTATGTCAG	10529
rs533581204	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21169266	GTGACAGGGGAAGAC[A/G]AAGAGTTGTTTTCAT	10529
rs533581256	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20941219	CAAATCCAGCAGCAC[A/T]TCAAAAAGCTTATCC	10529
rs533583146	snp	C/T	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:20941964	AAATGGAAGAACATT[C/T]CATGCTCATGGGTAG	10529
rs533593341	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21087251	TTTGCTCACTAAATA[A/T]ATGAGTCAGTAATTT	10529
rs533598732	snp	C/T	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:21116513	TAGGACTTCAACATA[C/T]GGATTTGGTAAAGAT	10529
rs533609977	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20890267	ATGTGCCATCTCGCT[C/T]CTACAAGTGTCCTGG	10529
rs533614828	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20907974	AAGCTATGCTGACAT[A/T]TTTTGGGAAAGAGGA	10529
rs533623196	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21080898	TATCACTCTCGCCCA[C/G]GCTGGAGTGTGATGG	10529
rs533626337	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21168512	TAAATGTAAAGTATG[A/G]GCGCTGATTGGATCC	10529
rs533631740	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20832553	AAAATTCAGAAAGCT[A/G]TACATATATAAATTT	10529
rs533644501	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21022193	CAGAGCTCAGAGCTG[A/C]TCCTCAAAGAACATC	10529
rs533648008	snp	A/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20941622	TAAAGGGTATTCAAG[A/T]AGGAAAAGAGGAAGT	10529
rs533650550	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20903392	GTGAATGTGGTGAAA[A/C]GGGAACACTTATACA	10529
rs533657304	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21096072	ATAGGATTAAATAGA[C/T]CCCATAAGCATGTCC	10529
rs533664042	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21093476	CATCAGTCCCTCCAT[C/T]GGCACTGAAAAAATC	10529
rs533665247	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20787390	CCTCAGAGTGATGTT[A/G]TGCTCTGCTAGAAGC	10529
rs533667850	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20786006	CACACCGACCCACAC[A/G]TAAAGTAACTATTAG	10529
rs533686365	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21086904	GCCACCCATAGGGAA[C/T]GTTCTCTGCCTGAAA	10529
rs533691072	snp	A/G	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:20978347	CCCGAAGAATAGAGA[A/G]CTTATTCAAGTAATA	10529
rs533691487	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20972347	TGATCAGGCAAACAC[C/G]AACTGTTTTTCTATA	10529
rs533698314	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21168717	AGGGATGAAATGTCA[C/T]GATGTATGAAACCAA	10529
rs533714527	snp	A/G			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20875654	AGTGGAAGTCAAGGA[A/G]ATGACTTTCACTTGG	10529
rs533714712	snp	G/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21022549	ATGTTCCAGGTAATT[G/T]GAGTTAACCCCATAA	10529
rs533715254	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	NEBL	GRCh38.p7	10:21176085	TCAGTGAGTGGCAGC[C/T]TCGACCTCCCAGGCT	10529
rs533721440	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21030601	GGTGGGGGAAAAGTA[A/T]CTCCAGCTCAACCGT	10529
rs533738190	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20839174	CTTCCTTCTCCTAAT[A/G]AGGCCTAATTAATGC	10529
rs533741594	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20892671	GCCCTCACCCACAAA[G/T]CCCACGTCTCCATTA	10529
rs533745486	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21086452	AGCCAATGAATGATA[C/T]AGAGAATTTCATTTC	10529
rs533748403	snp	C/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20980041	ATTCTTTTAAAGTGT[C/T]TCATTTCCACAAAAA	10529
rs533750279	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20831802	TTTTTCAGCTAATCT[C/G]AATTAAGAAGAAGAA	10529
rs533753416	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20932898	TATTTTCATCACAGA[C/T]TCAGACAGATGCCCT	10529
rs533759375	snp	A/C	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20821134	AGGGGTTACATCTGA[A/C]TAGTAAATTCACATT	10529
rs533762873	snp	A/C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20938076	TGTCCCTGTCTGACA[A/C/G]CTTTGAAGACAGTAG	10529
rs533764363	in-del	-/A	0.19607	0.244114	intron-variant	NEBL	GRCh38.p7	10:20967184	TTTCTATTTTCAAAG[-/A]AAAAAAAAAATAGGA	10529
rs533769568	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21056758	AAAGCAAAATACTGC[A/G]AGAAAGAAAGCAAAT	10529
rs533772859	snp	G/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21009801	CCTTCTGAAGCTAAT[G/T]GGTGCTCTAAACAAA	10529
rs533797088	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20794312	ATAATCAATTCTCCT[C/T]TTCTAGACTCTCATA	10529
rs533799649	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21123779	AAATCTTCAACATAT[A/G]TAATTTTATATATTA	10529
rs533801247	snp	G/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	NEBL, NEBL-AS1	GRCh38.p7	10:21175345	GAACTGCTTCAATCG[G/T]CCTGGCTCAAGGGAA	10529
rs533801914	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20947797	AGCACATGCTTCATG[C/T]GTAAGTGAGGTAAGG	10529
rs533816090	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20869061	TAGGGAAATTTTCTG[A/G]GGAATTGAGACCCTG	10529
rs533816557	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21092150	TACATTAAGCAGAAC[C/T]GGTCGTTATGTGCTA	10529
rs533821297	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20910195	TTAAAAATTATCTAT[A/C]TAGTTAAGCAAAATT	10529
rs533823917	snp	G/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20792737	CCTGTGAAGAGGAGG[G/T]TGCAGTGAGCTGAGA	10529
rs533829210	snp	A/G/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20877765	TATGTAGAAAGTCAC[A/G/T]CCTGGTCCAACCAAT	10529
rs533832819	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20926847	TCAATTTCTGAAAAG[A/C]AGAGAAACACAACCT	10529
rs533834208	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21169445	TCTGGCCACAACCAC[A/G]GGGAGCAGCTGATTG	10529
rs533839607	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21117948	TTTCTTACCTACCTC[A/G]GGGATATAGTGAGGT	10529
rs533840408	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20857567	TACAAAATGGAGCCA[A/T]ATGTGTCTTAGGGCT	10529
rs533849311	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20984859	CACAGCTCCCATTAT[C/T]GCCTGAGCTCCACCT	10529
rs533850282	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20893484	CATAATGTGGGTAGA[A/G]CAAGTGCAAAGCAGA	10529
rs533853927	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20869452	CATATGACTGATAAC[C/T]CTGACTTTCAGGCTG	10529
rs533864214	snp	C/T	3.30109e-05	0.00406256	intron-variant	NEBL	GRCh38.p7	10:20826432	AAAAGATAATTAATG[C/T]TGTAGAGAACTTACT	10529
rs533869427	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20816373	CTTAGGAATTAACTG[C/T]GGCAGAATTTTTGTA	10529
rs533873768	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:20978660	GCTACTCAGGAGGCT[C/G]AGGTGGATTGCCCGT	10529
rs533875418	snp	C/T	0.00199481	0.0315187	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20851865	AAACTTAAAGGGGAA[C/T]TGTTTCGTATATTTT	10529
rs533890183	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21062215	AGCTAAATTCTTAGC[A/C]ACTGAGCTAAGAAAA	10529
rs533891172	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21123024	TTCTAATAACAAGCC[A/G]GAAATTTTTTTGAAA	10529
rs533892535	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21121669	TACCCAATGCTAGGC[C/T]CACAACTTCAGTATC	10529
rs533893155	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20913320	ACTGCCGATCCTTCA[C/T]ATTGAACATCAGAAA	10529
rs533914261	in-del	-/CT	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21062231	ACTGAGCTAAGAAAA[-/CT]CTTTCACAACTCACA	10529
rs533928492	snp	C/T	0.000798403	0.0199641	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21129200	GGTCAGGAACTTGGA[C/T]CTACATAAGAAAGAA	10529
rs533933774	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21149339	TCTGTCACCCAAGCT[A/G]GAGTATAGTGGTGCA	10529
rs533939107	snp	A/C	1.65971e-05	0.00288067	intron-variant	NEBL	GRCh38.p7	10:20809916	TTTGCCAAAAGGAAG[A/C]AATCAACACTCATCA	10529
rs533939721	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20926176	TTTTGCTATGTTACA[A/G]GCAAAAAGAACTGGT	10529
rs533947092	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21044124	ACCATAGGCAGGGCA[C/T]GATGGCTCACGCCTG	10529
rs533949060	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20862426	AATTGTTTCTAACCT[C/T]GCTCTTTCTGTAAGG	10529
rs533951968	snp	A/G	0.00914312	0.0669923	intron-variant	NEBL	GRCh38.p7	10:21061529	TATTATATATCACAT[A/G]TTACATCATATATTT	10529
rs533952129	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21068098	GAATTTCTCTACTAG[A/G]TGGGAAAAAAGGCTA	10529
rs533955492	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20927902	ACGAAGCTTTCATCC[A/T]GTAAGATAGTGTCAC	10529
rs533956212	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21076343	CCAGCTACTCAGAAG[G/T]CTGAGGCAGGAGAAT	10529
rs533958960	in-del	-/A	0.336702	0.234484	intron-variant	NEBL	GRCh38.p7	10:21152583	TGTCCAAGAAAAAAG[-/A]AAAAAAAAAAAATCC	10529
rs533988089	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20898651	CCACTTAGAGATCTA[C/T]AAGGCATATTGACAT	10529
rs533989062	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20863017	AAAATACTGTATAGG[C/T]ATATAGGATCAAACT	10529
rs533989754	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20921772	ATCCATGCACACACA[C/T]ACATGTACATGCACA	10529
rs534002666	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20856949	TTCTCCTGCCTCAGT[C/T]TCCTGAGTAGCTGGG	10529
rs534003373	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20780886	ATAAATCGGTGATTT[A/G]CTTTTAAACAAATAT	10529
rs534003843	snp	C/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20872005	ACTGTTTCTAAGTTA[C/T]TACATTCATATGAAA	10529
rs534012123	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21067676	ATCTGAGAGAGAACA[C/T]CTTCCTATTAAAATG	10529
rs534023006	snp	A/T	0.000798403	0.0199641	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21128747	TAATTGTTAAAACAC[A/T]TTTTTTAAAAGTGTG	10529
rs534024228	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20892890	ATTCAATACACCCTG[C/G]AAGGAAAAACAATGG	10529
rs534025528	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20816374	TTAGGAATTAACTGC[A/G]GCAGAATTTTTGTAA	10529
rs534035879	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21073899	CTAACACGGTGAAAC[A/C]CCGTCTCTACTAAAA	10529
rs534036313	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20954698	ACACAGGAAGAGGAG[A/G]GGGCCTGGCTCCCCC	10529
rs534037220	snp	C/T	0.000798403	0.0199641	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21136925	GGTAGAATTAATGGA[C/T]ATCTAGAGACAATAT	10529
rs534040133	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20967550	GGAGAATCACTTGAA[C/T]CTGGGAGGCGGAGGT	10529
rs534042469	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21006157	TTCTTTGGTGCAGAT[C/T]ATCAAAATGTAACTC	10529
rs534054420	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21032400	CTTCTGGGATTTTGG[G/T]GTCTAAGATGCTTTT	10529
rs534059182	snp	A/G	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21136403	GCACCATCACAGCTC[A/G]CTGCAGTTTCAAACT	10529
rs534065500	snp	A/T	0.00159617	0.0282053	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20785503	AATCAAAGGAAACCA[A/T]GAACACAATTAGCAG	10529
rs534067036	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21099190	CTTTTTCATAGACAT[A/G]TCATTTTTTAAAATG	10529
rs534072641	snp	A/C	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20840147	TTCAAAATATGGGGA[A/C]AAGGCTTTAAGCTCT	10529
rs534076352	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21073785	GAATGCTATGAAATG[C/T]CTACTATAGCCAGGG	10529
rs534077238	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20935462	CAGAACTGAGAACAC[A/C]CCCAAGAACATGCTC	10529
rs534078006	snp	C/G	0.0126979	0.078662	intron-variant	NEBL	GRCh38.p7	10:21155006	GAGTTCGAGACCAGC[C/G]TGGCCAACATGGTGA	10529
rs534082096	in-del	-/AATACTATACAGCCACAAA	0.00159617	0.0282053	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20853463	ACATATACACAACGG[-/AATACTATACAGCCACAAA]AATGAACGAGATCCT	10529
rs534082484	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20915807	AATGGTATTTCTAGT[C/T]CTAGATCCCTGAGGA	10529
rs534093321	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20949171	CCCTGGCCAGAACTT[A/C]CATTCTCAGCAAACT	10529
rs534102665	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21103020	GCATATTGTTCCCCT[C/T]CTTGTGTCCATGGCA	10529
rs534115637	snp	A/C	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21115405	CTTTCTGTCTAAAAG[A/C]CTTCTGTTAACATTT	10529
rs534120861	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20809308	GCAATCTAAGTTAAA[A/C]GCCAACTATGCTTGC	10529
rs534129505	in-del	-/AA	0.0832709	0.186283	intron-variant	NEBL	GRCh38.p7	10:21024509	AGAATAAGATCTTCC[-/AA]AAAAAAAAAAAAAGA	10529
rs534135046	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21079262	AGAAAAAGAAAGAAA[A/C]TGAGGAGGTGAAGAG	10529
rs534138088	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21161026	TTGTTCCATTGCATG[G/T]CAGTGACCCGTAATC	10529
rs534160397	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21125105	GAACAGTCCTATGGC[A/G]GCAAAGAAGAGACAG	10529
rs534168653	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21009103	CTGTCCAATAGCAGA[A/T]ATATAGTTAAGAGCT	10529
rs534173524	snp	C/T	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20961441	GAAAGCTGAGAACCA[C/T]TCAAAATGGAATAAG	10529
rs534177860	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21167412	GTTCAGCCCAAAAAT[A/G]TGTCTGTGAATAATG	10529
rs534177947	snp	C/T	0.00874735	0.0655527	intron-variant	NEBL	GRCh38.p7	10:20789020	AATTATTACTGTCCA[C/T]TATGTTCAAGGCATG	10529
rs534178262	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20888286	ATAAGTAGAAAAGAA[G/T]AAACTTTCTCCCAAA	10529
rs534191375	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20949451	ACATGTATCCCAGAA[C/T]GTAAAGTAAAAAATA	10529
rs534194258	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21026728	GTGAAAATGAGTTAA[C/T]ATGGCAGGGCTGCCT	10529
rs534205750	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20828059	AACCTGCACAGGTAC[C/G]CCCAAACTTAAAATA	10529
rs534206817	snp	A/G			utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	NEBL, NEBL-AS1	GRCh38.p7	10:21174001	GTGCACGGGGAGGGC[A/G]ACGGGGCCTGGCGCC	10529
rs534215829	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20882326	AAAGAAAGAAGAGGG[C/G]AGAGGAGAGAGGAAA	10529
rs534218903	snp	A/T			intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20958782	TGCAGTATTTAACAA[A/T]TCTCCCATGTTCAAT	10529
rs534227354	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21024073	TTACTCTGGGGAAAA[A/G]AAAAAAAAACATTGA	10529
rs534235359	snp	A/G	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21128141	ATAACCAAATTCAAA[A/G]GAAACACAAACAGTA	10529
rs534238277	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20954111	CTATTTACTGAATAG[A/G]TATTTATTTGATAAC	10529
rs534245421	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21109689	AGAACTTGTTGTTGG[C/T]CTATTCAGAGATTCA	10529
rs534257329	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21032917	TCAAAGGGATTATAC[A/G]GTAAACCTGACCTAC	10529
rs534259323	snp	C/T	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:20915175	ATGAAAATAAATGAA[C/T]CCATCACTGTAATAA	10529
rs534273919	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20805338	TTCACTTAAATTAAA[C/T]TAGCATATTCCAATG	10529
rs534283458	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21154717	CTGGAATCTCTTTAT[G/T]GCCTTTATTAACTCT	10529
rs534288238	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21060091	AATGCCCGGTCATCT[A/G]AAAAATAGCAGCTGG	10529
rs534291132	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21148821	GTGAGCCACCACGCC[C/T]GGCCCCTGTCCTCCT	10529
rs534299022	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20964876	AGAAATACCAGGTTT[A/G]CCCGTTACGTGAGCT	10529
rs534305781	in-del	-/C	0.00358779	0.0422022	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21136469	AAAGGGCTGAGATAA[-/C]AGGCATGGGCCACCA	10529
rs534322430	snp	C/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20847912	TATATTTTATTTTCA[C/T]GTTGAAAATCAGGTC	10529
rs534325318	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21115715	TTCTAACTGGAGCTT[A/T]TTGAAATTTTGGGTC	10529
rs534327391	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21161956	GGTGGCTCAGTGCAC[C/T]AGAAAAACCAACTCT	10529
rs534328431	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20993093	TGGCCTGCAACTACA[A/G]AGTCTTTTAGGGAGT	10529
rs534329998	snp	C/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20861947	ACAGCTTCGCCTGGC[C/T]TACCTTAAACATGCT	10529
rs534345873	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20923760	TTTAATGTTGAAGCT[A/G]TCAAGCCTGCACTTC	10529
rs534346695	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21059309	CACAGGCACTCTATC[G/T]GTTGGATGCTGAGTG	10529
rs534352151	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21065678	TATTGAGCACCTGCT[A/G]TGTATGAGGATTGCC	10529
rs534352887	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:20994621	CTGCATATAACATTT[C/G]GTCCCCCAAAAAACT	10529
rs534359181	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20957446	TTATAAATGGGTATG[C/T]GAAATTGAAAGTGGT	10529
rs534365075	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20806261	CATCCAAGCAGAGGC[C/T]CTCCGAATTCCTGAT	10529
rs534378237	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20909404	AACATGCAATGTTTG[C/T]CTTTCTGGGTGGCAC	10529
rs534378306	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20799973	AAAGAGAGAGCGCAC[A/G]CGTGTGAGAGAGCGA	10529
rs534381272	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20918005	CAAAATGATATATGC[A/G]TGACACAATGAAAAT	10529
rs534381281	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21030303	AGGAACTGGAACGGT[A/G]GAGGACAGGAAGTGA	10529
rs534382445	snp	A/T			intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20831254	GGGATATCCATGCTC[A/T]CTTGCATTCCTTTCC	10529
rs534394765	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20986244	ATGCAAAGCAACCCA[A/C]CAGTTCAAAGGTTGG	10529
rs534410708	snp	C/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21152304	AGGACAGTGACGCCA[C/G]TGTAATATTTTAAAT	10529
rs534411067	snp	A/G	0.000798403	0.0199641	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21146275	CAGGCAGCATCATTT[A/G]CATCACCACGTGGCC	10529
rs534414555	snp	C/T	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:21071891	TGGTGCAATCTTGGC[C/T]CACTGCAGCCTCTGT	10529
rs534418433	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20951205	AACATGACTTCCTAC[C/T]TCTTGTCCTTGGAAC	10529
rs534424414	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20836474	GTGATCCACCCACCT[C/T]GGCCTCCCAAAATGC	10529
rs534427355	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21156661	ACAAAAGTCTATTTC[A/T]CTCACTCTTGAAATA	10529
rs534440530	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21112874	ACATATTCATAGACA[C/G]TATTTAGTATCTGTG	10529
rs534443913	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21023555	AAAAAAATAGCCAGG[C/T]ATGGTGGCGCACACC	10529
rs534449038	snp	A/C	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21152008	AAGTACTTAGAACAG[A/C]GCCTGGTTCATAGGA	10529
rs534449746	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20824557	GAGATCTTTAAATGT[C/T]AGAGAATCATATCTT	10529
rs534455223	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20842863	TTGACTATCACCTTG[C/T]CATTCCTCCCACCCT	10529
rs534457039	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21158559	ACGTCAGCCCCAGAA[A/G]GGAATGGTCCCTTCA	10529
rs534464075	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20904273	CTTTTTGCACCTATT[C/T]GTAAATGCATTTCAG	10529
rs534468422	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:20973565	TACCATTTTTTTACA[A/T]AGAAAAAATGTATCA	10529
rs534468585	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20873118	ACATTTCTCAATAAG[C/T]ATTTGCTCCAATCTA	10529
rs534483645	snp	C/T			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21142145	GGTAATATAACCCAC[C/T]ATTCCTAAGCATTCA	10529
rs534485548	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20829878	TTTCCAAGAGCAAAG[C/T]CATGTCTAGTTTTGC	10529
rs534488949	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20871529	GTTATTTTATTTCAA[C/T]GAAACATTTATATAC	10529
rs534489004	snp	A/T	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:21078660	TAAAGGTTTTGATTG[A/T]TTAATAAAGAAAAAT	10529
rs534496463	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21035331	ATGCTCTCCTTCCCC[C/T]CGCCCCCCAAAATTA	10529
rs534496804	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21017134	CAGCTAAGTGTGAAA[C/G]GGCAGGTTATCGAAA	10529
rs534497307	in-del	-/AAC	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:20895322	ACTACTAATAATAGT[-/AAC]ATAATAATAATAAGG	10529
rs534499452	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20938538	TCAGAGCGCCTCTTC[A/T]CCTTAAAAGGAATGC	10529
rs534503706	snp	C/T	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:20796654	GAATTTCTGCTATTT[C/T]ACTTCAGAATAATCT	10529
rs534504893	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20904774	GACTTAATTACTTCT[C/T]ACATCTGGAAAAACT	10529
rs534514500	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20899833	ACTCATCACTCAACA[C/T]TTGCTGGATGAAGTC	10529
rs534520615	snp	G/T	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:21049432	ATTTATTCTAACCAA[G/T]CTCATAAGAAGATTG	10529
rs534522980	snp	C/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21121028	TCCCTGGAGTAGAGA[C/G]GAGGCATCTGAAAAC	10529
rs534526253	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21091233	AAATGTCTACACATG[A/C]AATTCCATTGTTGGG	10529
rs534534227	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20946232	TTTCCTCCAAAGTCT[A/G]CATGTTGTTTCTGCA	10529
rs534540356	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21076086	TTATGCATTATCAGC[A/G]GTAATGTAAAATGGT	10529
rs534544320	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21085171	TGAGGACCCATTATA[A/T]TTCTCACGCTCCATC	10529
rs534548205	snp	A/G	0.000798403	0.0199641	utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	NEBL, NEBL-AS1	GRCh38.p7	10:21173994	CGGGTGAGTGCACGG[A/G]GAGGGCGACGGGGCC	10529
rs534549918	in-del	-/A	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:21045994	GGCAGATGAATGGAT[-/A]AAAAAATGTGGTACA	10529
rs534553157	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21040683	CATTTCTTTTTTTTT[C/T]CTTTATGGTTTGGAT	10529
rs534582416	snp	A/G	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21140032	TAGGCGTGGTTTCAG[A/G]TGCCTGTAATCCCAG	10529
rs534583223	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21018441	CAGAGGTGTTCTTGC[C/T]GGCCTCCATAATAGT	10529
rs534588112	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20982854	ATATCAGGGCAATCA[C/T]ATCTTAAGAATGCCA	10529
rs534591268	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20890497	GTGGGCTTCCTGTTA[C/T]TAATTCCTCCCAATT	10529
rs534593879	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20946663	GACGAGGTTTCACCA[C/T]GCTGTTGGCCAGGCT	10529
rs534600135	snp	A/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20806771	AGTAAACATTTGGTG[A/T]CTAAATGAATGAATG	10529
rs534603328	snp	A/G	0.00716266	0.059414	intron-variant	NEBL	GRCh38.p7	10:20941017	GAGGTACAAGAAGGA[A/G]CTGGTACCATTCCTT	10529
rs534612931	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20807078	CGCCTCTGATCCCCG[C/T]ACTTGGGAGGCTGAG	10529
rs534617097	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21001194	CAGGTCCAGCCAGCC[A/G]ACAGACCGCCAGAGA	10529
rs534621300	snp	C/G/T	0.000165021	0.00908222	utr-variant-3-prime, synonymous-codon, nc-transcript-variant	NEBL	GRCh38.p7	10:20785807	CCCTGTTCTCTGCAC[C/G/T]GTGCCGTACATCCAG	10529
rs534623910	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21046376	AAATAGATTTTGTAG[C/T]GTTATACGAGGTAAT	10529
rs534630968	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21117955	CCTACCTCGGGGATA[C/T]AGTGAGGTTTAACTG	10529
rs534634186	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21007336	GCAGCCTTATACAGA[A/T]AAGTTACAGGAAGTA	10529
rs534637435	snp	C/T	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20977900	ACTCAAGCCTAACGT[C/T]CCTGCTCATCTCTAG	10529
rs534653277	snp	C/T	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21132234	ATAAATGGAATCATA[C/T]CATATGTGGCCTTTA	10529
rs534654366	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20831064	CAAGTTTGGCCAATG[A/G]TTTCTTAGTGAAAGA	10529
rs534655137	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21125014	AGTCTCCACTGAAGT[A/G]CAGTGTTGAGAGGTG	10529
rs534656276	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20965302	GTGGGAAGCGCTAAG[A/G]GAGAAAAATAGCGAG	10529
rs534663495	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21101708	ATTTATGTTCCACTT[C/T]AGAAGCTCTTCCAGA	10529
rs534663582	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21107358	TCAATACCTAGTTTA[C/T]TGAGAGTTTTTAGCA	10529
rs534663796	snp	A/C	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20936153	TAATAACAAAACTAC[A/C]AATTATTAAGCACAA	10529
rs534672146	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20867830	TCATATATTAAATTC[C/T]TATACATACTGGAAT	10529
rs534682277	in-del	-/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20937454	AAGTTGAAAGAGCCA[-/G]GGGGTGGAGACAAGA	10529
rs534689109	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20896755	TCTGGATTAAGAATG[A/G]GGAGACTTGCTCTAG	10529
rs534698273	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21166168	GAGCTTGCAGTGAGC[C/T]GAGATCAAGCCACTG	10529
rs534715982	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20854953	TTTTTGGCTAGGCGC[A/G]GTGGCTCACACCTGT	10529
rs534720768	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20958228	TTTGGACACTGTCCC[C/T]TAAGAATATTTTCCT	10529
rs534747047	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20972482	AGGTGCAGTGGCTCA[C/T]GCCTGTAATCCCAGC	10529
rs534750990	in-del	-/A			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21135435	AGCCTCAGTGGAGAT[-/A]AAAAAAAAAAAAATC	10529
rs534756176	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:21048822	CCAACATGGTGAAAC[C/G]CTGTCTCTACTAAAA	10529
rs534757396	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20995894	CCACCAACTTACCCT[C/T]TGTGGGACTAATTCT	10529
rs534768800	snp	A/C			utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20785430	ACTACATTTAAGGGA[A/C]AATCAACTTCTCTAT	10529
rs534770576	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21071350	AAAAATGAATTTTTT[C/T]CTAAAATTTTAATTT	10529
rs534783475	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20937132	GCACACAGACTTCCC[A/C]AACTCTCCCAAACCA	10529
rs534785819	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20837060	TATTGAAATTGGGCC[A/G]ATTAGTAACCCTACA	10529
rs534798177	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20891740	ATATTTTAAATGAAG[G/T]TGTATTTAAAATTTA	10529
rs534798774	snp	A/G	0	0	intron-variant	NEBL	GRCh38.p7	10:21112510	TACCAAACACCACAT[A/G]TTCTCACTCATAGGT	10529
rs534811171	snp	A/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21051895	CTTCACCTATGAGGG[A/T]GTGGTGGTGTGCTGG	10529
rs534811551	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21067249	GTGCTGAGATTACAG[A/G]TGTGAGCCACCGCGC	10529
rs534820541	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20988325	CACATTACTCTGCCT[C/T]CTCAACATTCCATAT	10529
rs534833824	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21076743	GAGGACATTATAATT[G/T]AAATCAGCCAGTCAC	10529
rs534840576	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21157967	CATAAGCCAAGGACA[A/G]GGGCCTGAAACAGAG	10529
rs534843126	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21167817	ATTTTCTCGGCACCT[C/T]TTAGTGATAACAATT	10529
rs534843716	snp	C/T	0	0	intron-variant	NEBL	GRCh38.p7	10:21094012	ATCTGTGGTTTGACA[C/T]ATTAAGCATCACTAC	10529
rs534847033	snp	A/T			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21139557	TAGCCTCATGTTGTC[A/T]TAGCAATGATGAAAT	10529
rs534866635	snp	G/T	0.00438332	0.0466095	intron-variant	NEBL	GRCh38.p7	10:20912935	TTACCCAGGCTTTAA[G/T]GTTTTTGGTAGACAC	10529
rs534868609	snp	C/T	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:20906480	ACTATAAGATAATAT[C/T]AAAATAAAATTATAA	10529
rs534876955	snp	A/G	0.00279162	0.0372561	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21137963	GAAGGGAAGGGAAGG[A/G]AATGGAAAGGAAGAA	10529
rs534879967	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20843396	GAGCCCTTTCCTACC[C/T]TGATGCATGTATTCT	10529
rs534880112	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20892258	GTGGAAATCTTCCCA[A/G]AAGTGCTTCTAGTGT	10529
rs534882300	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21100364	GAAGAAGCTGAAAAA[C/T]GAGGAGCTCACTCGC	10529
rs534884014	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20886302	CTGAGGTGGGCAGAT[A/C]GCCTGAGGTCAGGAG	10529
rs534888005	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21106027	TTCCCACTTTTTGAT[G/T]GGGTTGTTTGTTTTT	10529
rs534891174	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20990243	AAAAGGGTCCATGGC[A/G]TACAAAAAGCTTAAA	10529
rs534899742	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21082897	CCTCCCAAATAGCTG[A/G]GATTACAGGCGCCTG	10529
rs534905071	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20815043	AGGTGTAAGATATGG[A/G]TACCACTTACTGTGG	10529
rs534919374	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21020034	GACCCAGCAGGAACA[G/T]TACGAAGACAAGAAT	10529
rs534925117	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20850592	GTTCTAAACTAGTCA[A/T]CTTGTTGTCTAAAAT	10529
rs534943446	snp	C/G	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:21105690	GATTTATAATCCTTT[C/G]GGTATATACCCAATA	10529
rs534954309	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20983291	AACAATTATCTTGAG[A/T]CCATTTATAATAATC	10529
rs534957803	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20803727	CACCTTCTCACCAGA[A/G]CCCAGCAGAGCACAC	10529
rs534962742	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21082358	AGTGTTCTGATTTGG[A/G]TGGTTAGAATGTGGT	10529
rs534968352	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20941287	CCGGTTCAACATACG[C/T]AAATCAATAAACGTA	10529
rs534975479	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20888858	AGTATTTATCTGCAC[A/G]GGAGAATGGAACATA	10529
rs534975541	in-del	-/T	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:20989736	CCATTATATCTGAGG[-/T]GATTCTTGTTCCTTG	10529
rs534983744	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21020627	TGGCTTCTGGCTTCC[A/G]TTTCTAGAAGTTTCT	10529
rs534999559	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21046550	TTTGTTTTCTGCTTT[A/G]AAAAATTTGGATTCT	10529
rs535024310	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20991036	CCTAACACATACTCT[A/G]ACATTTGACAGCTTT	10529
rs535029944	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21027414	ATCACCGCAGCCTCG[A/G]CCTCCTGGACTCAGG	10529
rs535032799	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20936668	CTTTCTTGGCAACTT[A/C]TCACTGAATCTAAAT	10529
rs535052134	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21052653	AGATTAAATGGCATG[A/G]TCTTGAAAGAGCATG	10529
rs535056765	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20920316	ACCCTCAGGGGTACT[A/G]GTAAAAAATATGAGA	10529
rs535062342	in-del	-/A	0.0144733	0.0838281	intron-variant	NEBL	GRCh38.p7	10:20980391	AGAACCAGAAAAAGA[-/A]AAAAAAAATATATTT	10529
rs535069059	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21168517	GTAAAGTATGAGCGC[C/T]GATTGGATCCTGGCT	10529
rs535072896	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:20997012	TGGGTTATTTATCCA[G/T]AATCATAAACATTTA	10529
rs535079659	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20980608	CTTGGTAAAGTATCA[G/T]CCAGGGGCCCTAGAA	10529
rs535088526	snp	A/G			intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20961905	CTCAGCCGGAGGTGC[A/G]GTTAAGAACCAGAAG	10529
rs535091089	snp	A/G	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:21004069	AATTTTTTCTTATAC[A/G]CATACACATAAGTAC	10529
rs535096268	snp	A/G	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21138522	TCAGGGTTCAATAAA[A/G]TGTCATCGGGAGAGG	10529
rs535096650	snp	A/C/G	0.00637159	0.0561118	intron-variant	NEBL	GRCh38.p7	10:20819761	ACAAGGTCTTGCTCC[A/C/G]TTGTCCAGGCTGGAG	10529
rs535097378	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21029583	GGATTCTGACAAAAC[A/G]GATACAGACTGGAGG	10529
rs535102568	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21064029	ATGAACTGAGATCGC[A/G]CCACTGTACTCCAGC	10529
rs535102867	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21071233	TAAATAATATTATTA[C/T]TATTTTTAAAAATAA	10529
rs535102917	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21065307	TTGTTTAACCCACAA[A/C]TGAATAAAACTGTTG	10529
rs535107502	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20863983	CAAACCAATTAATAC[C/G]CCTTGCAATTTAAGG	10529
rs535108399	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:20973751	CAAGTCAAGAGGTTT[C/G]ATTTAGGAACTAGAA	10529
rs535109814	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20782192	CCCTACCACAAAAAT[A/G]TCAATCATGTGTAAT	10529
rs535112787	snp	A/C	0.000798403	0.0199641	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20855530	CAAAACAAAACAAAA[A/C]AAAAACGAAGGAAAA	10529
rs535113549	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21067250	TGCTGAGATTACAGG[C/T]GTGAGCCACCGCGCC	10529
rs535118012	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21058031	TCACTTTGAAAACAG[A/G]GCAAATTTCATGTCA	10529
rs535123473	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20788939	AGCAAATATTTATCA[A/G]TTAATGCGTGCACAG	10529
rs535136435	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20782678	GTGGTGTATGGAGGT[C/T]GAGGAGACCTGGGAT	10529
rs535137684	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20894814	GGCGCCTGTGGTCCC[A/G]GCTACTCGGGTGGCT	10529
rs535141458	snp	A/C	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20938502	GAGACACCAGAGCAG[A/C]AAAGCTGAAAATTCT	10529
rs535163003	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20932135	CTTCTTTTCTCCATT[C/T]CAGTGGCCACCAGCT	10529
rs535165677	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20899724	TTCATTTGTTCAACA[A/G]ATAAATGTTGTTATG	10529
rs535166394	snp	A/G			utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20781931	GAAGCAAATCGCTAA[A/G]GTATAATTAATTTAT	10529
rs535184905	snp	A/T	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21145256	AATATATAAGCCTTC[A/T]GGCTTGGCAAAATCT	10529
rs535185987	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21063882	CTCAAAAAATAAATA[A/C]ACAAATAAATAAATA	10529
rs535189039	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21026220	TTGGCAATAGGCAAC[A/G]TCCGGAGACATTTCT	10529
rs535198682	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20966640	GACAGCCTGGACACC[A/G]GAGCAGTTCTGGACC	10529
rs535200139	snp	A/C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21157266	GAGGTGTCATTGATA[A/C/T]ACAAAAAATTAACAG	10529
rs535201655	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21021144	CACATCCAATCACTC[A/G]TTCACCAAATCTATT	10529
rs535214016	snp	A/C			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20867986	CTGGTCTTCATTTTC[A/C]TACTTTTAAAGGCTA	10529
rs535218319	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20808208	TAGTGTGTATATTTA[C/T]CACATATAACTCCTG	10529
rs535224566	snp	A/G			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20863140	GCATTGTAGCTCCCC[A/G]TAACTGCACAACTTC	10529
rs535228535	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	NEBL	GRCh38.p7	10:20817107	AAAGTCACCCAGGCC[C/T]GGTGGCACACATCTG	10529
rs535254549	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21040209	CGTCTCTACTAAAAA[A/T]ACAAAAATTAGCTGG	10529
rs535255687	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20925916	CACAATACTCTTATT[C/G]AGTAGGTGTCCTGGA	10529
rs535259281	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20959750	CTTATAAGACTGCTA[C/T]GGCTGCTAACATTAA	10529
rs535260416	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20888974	TTTATTGAGCACAGA[A/T]CCTGTGCTAGCCTTC	10529
rs535262817	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21063485	GAAATCCCTCTTTAA[C/T]GAAATCCATGGAAAC	10529
rs535265791	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20791858	GCAGAGTGCGTGAAA[A/G]AAGAGAATATGATTA	10529
rs535269508	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20977081	TCAGTTTCAGTCAAA[A/G]ATAAAGTTTCCAGTC	10529
rs535282915	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21028056	ATGTGGTGAAACCCT[A/G]TCTCTACTAAAAATA	10529
rs535303764	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20930582	AGTCTCTCCTACTAA[A/C]TCCTACACCAGTTCC	10529
rs535312145	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21045997	AGATGAATGGATAAA[A/T]AAATGTGGTACACAC	10529
rs535318592	snp	C/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20849610	CTCTGTCTTTCCACC[C/T]TCTGCCATGGGATGA	10529
rs535320817	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21069678	AAATGGTTCATGTTA[C/T]ACATTTTCATACAAC	10529
rs535333791	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21150649	TTCCATATTTCAAAA[C/G]TTTAAAAGACAGAAT	10529
rs535334105	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20962901	ACATGGAATGGCTGT[G/T]TCTGTTGAATCATGT	10529
rs535334796	snp	A/G	0.00478085	0.0486577	intron-variant	NEBL	GRCh38.p7	10:20805950	TCTTTGAAGAAGTAT[A/G]AAATTCCTCCTTTAA	10529
rs535336853	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20800165	ATTGTTTTATTTTCT[A/G]TCTCTGTAAATTTGA	10529
rs535338632	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20952917	CTCAAAAAAAAAAAA[A/G]AAAAAAAAGAAAAAG	10529
rs535341126	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20838586	CAATGGGTTTGAGAG[A/G]TTGGTCTCTAATCTT	10529
rs535349497	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20880661	ATTCAGATGTACCTC[G/T]GACTGATAAGAAATA	10529
rs535352704	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:20975522	GCAAGAGCTATTATA[G/T]GGATTGTGTATGTTT	10529
rs535354094	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21081605	ATGACACTCCAATAG[C/T]AACAAGCATACTTAA	10529
rs535373864	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20922407	TGTGTACAGTGATAC[G/T]CCAATAAATTCATAG	10529
rs535377141	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21156375	GGATCTGATTATGAG[A/G]AGGAAAAGAGAGCAG	10529
rs535394769	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21094224	TAGCCAGGTGTAGGC[C/T]GGAGACGGTGGCTCA	10529
rs535396474	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21052481	TCCAGCCTTGCTCAG[C/G]ATCTACAAAGCCCAC	10529
rs535397886	snp	A/C	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21146138	GAAAAAGAAACTGTG[A/C]ATTGTTAAACAAAGT	10529
rs535398690	snp	C/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21124124	GCTTTTAAATCATAA[C/T]ATTGCCTACTAGACC	10529
rs535401943	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20863128	GCTACAGTGACGGCA[C/T]TGTAGCTCCCCATAA	10529
rs535407570	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21000666	GATAGAAGGTTAAAT[A/G]CTTACTGCAAACAGA	10529
rs535409020	snp	A/G	0.000798403	0.0199641	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21130317	GTTGGAAATTTCAAC[A/G]CCCCTCTATCAGTAC	10529
rs535410964	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20899114	ATATTTTATTTGTTC[C/T]GTAAAAGGAAAGAAT	10529
rs535417695	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21106739	AAGTCAGTAGTAGCT[C/T]GATGGGGATAGTATT	10529
rs535437414	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21050640	GCTTAATTTGACTGC[A/G]TAGATTCCAAGGGCT	10529
rs535438325	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21151965	CGAGGGCAGGAATTT[G/T]CCTCTACTTTGCTCA	10529
rs535457966	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20816694	GAACCCAATCTATAT[A/G]TTAATGACTGTAAAA	10529
rs535466807	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20822019	TGCCACTGCATAGCC[C/G]TCCTTCTGCGTTTGC	10529
rs535471714	snp	C/T	0.00557542	0.0525036	intron-variant	NEBL	GRCh38.p7	10:20910338	TAACTCATGAGCTAT[C/T]TAATCATGTAGCTTC	10529
rs535474906	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21017074	GAAAAGTGTGGACAT[C/T]GAGGGCTCAGAGATC	10529
rs535474985	snp	G/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20860428	TCTAAATTGTTTGTC[G/T]CCTTTTAAAGCACTC	10529
rs535485735	in-del	-/AAAA	0.0111196	0.0737302	intron-variant	NEBL	GRCh38.p7	10:21151512	CAACCAGCCAAAGTG[-/AAAA]AAAACTTAAAACCTA	10529
rs535496392	snp	C/G	0.000798403	0.0199641	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21137844	GCTTCTCGGGAGGCA[C/G]AGGTAGAAGTATCAC	10529
rs535498899	snp	C/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20862025	AGCCTGTTTTACACA[C/T]GTTGAACATCTCATA	10529
rs535500544	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20801417	GGCCAGGCTAGTCTC[A/G]AACTCCTGACCTCAA	10529
rs535503500	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21106192	AGATCTTTAGTTTAA[C/T]TAGATCCCATTTGTC	10529
rs535532989	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21070773	CAGGGGATAAGGAAA[C/T]GGAGTCTTTATTGAG	10529
rs535543596	snp	C/T			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21142776	CCCTGCTATGAACTG[C/T]GCGTGTGAGGGATCC	10529
rs535543922	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20934273	CAAATTCGGCTGTCA[C/T]GAGAATATGACAAGC	10529
rs535557445	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21034573	TATTTCCTAACTTGT[A/G]TGACTACAAAAGCAA	10529
rs535561918	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20836677	GCCTGGCCTCTCCTA[C/T]TCCTGTGTGGAACCT	10529
rs535568547	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21112003	AATGCTCATCATCAC[C/T]GGTGATCAGAGAAAT	10529
rs535584103	snp	A/G	0.0134861	0.0810011	intron-variant	NEBL	GRCh38.p7	10:21041014	CTTTATTAATTACCC[A/G]GTCTCAGGTAGTTCC	10529
rs535597219	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20978673	CTGAGGTGGATTGCC[A/C]GTACCCAGGAGTTTG	10529
rs535599554	snp	G/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20829264	TGCAGCCATAAAAAA[G/T]GATGAGTTCATGTCC	10529
rs535600945	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20928233	AGTAAAATTTTTCCA[A/G]TAACTGAATTGAGTA	10529
rs535606598	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20934638	CTGGATACGAGAGGT[G/T]CTAGACAGAAGGGGC	10529
rs535609787	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20823603	GAAAAAAACCTTGTA[C/T]ATTATCGTAAATAAA	10529
rs535611119	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20981824	GAAGACATGAATTGA[A/G]AGATAGAAATAAACA	10529
rs535626537	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21117863	AACTCGGCCGCTATT[A/G]TCTCTATGACCTTAC	10529
rs535628323	snp	C/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21110943	AAGCATTCCTATGCA[C/G]CAATAACAGACAAAT	10529
rs535634565	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21062927	GAACAGAGAAGGACA[C/T]GAGCGGCCAAGCTGT	10529
rs535637036	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:20978810	AATCAAAACAATTGC[G/T]GCTAAAAATAAAAGT	10529
rs535645730	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20811588	TGGAATCCTTCTTCA[A/G]AAAATACTTCCAGAG	10529
rs535663681	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20852885	AGGCAGAGGACAATT[A/C]ACCGCAAACATAATG	10529
rs535666349	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20935150	GAGGAAATTCAATCA[A/G]TCCTTCAACACAGTG	10529
rs535666731	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21124736	GGTGGGAGGATTGCT[G/T]GAAGGCTAGGAGTTT	10529
rs535675522	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20883127	TGGTTGGACCATTCT[G/T]AATTAGAACTGTTAG	10529
rs535675593	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21114463	TAGTGTTGTTCAATT[A/C]TTCTGTATTCTTACT	10529
rs535681484	snp	A/C	0.00438332	0.0466095	intron-variant	NEBL	GRCh38.p7	10:20895324	TACTAATAATAGTAA[A/C]ATAATAATAATAAGG	10529
rs535690436	snp	C/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20818158	GATAAACAGTGTTGA[C/G]CCTCATTATCTCCAC	10529
rs535697831	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20812364	TCTAGGGTACATGTG[C/T]ACAACATGCAGGTTT	10529
rs535701146	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21170267	CCTCCTTCCCTCCCA[A/G]TCCCTTCAGGCCTAC	10529
rs535703832	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20847352	GGGAATATATGTCAG[A/G]GAAAACATGTCTCAC	10529
rs535716154	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21088338	AGACCCTATTTCTGA[G/T]AAAACATTTTAATTA	10529
rs535739664	snp	A/G			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21130368	AAAATCAGCAAGGAC[A/G]TAGTTGAATTCAACA	10529
rs535744841	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20929928	CTATAAAAAATAAAA[A/G]TAAAAAAATTGAGGT	10529
rs535746724	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21116471	ATTACCAAAGTGTCC[A/G]TCTCCAATTATCATC	10529
rs535753326	snp	A/G	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20955327	TGTGTGAAATGAGTG[A/G]TACAAATGATAGTGT	10529
rs535767481	snp	A/C			utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20785621	GGTACCTGTGTGTCT[A/C]ATTGTCAAAGGAAGG	10529
rs535776902	snp	G/T	0.00119737	0.0244387	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20848407	AAAATGGTTACTTCA[G/T]ATTTCTTTATCAGAT	10529
rs535776958	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20818648	TTAACTGCATTTTTT[A/T]AAAGAGATTTACCAA	10529
rs535778404	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21003195	TTCTGCAGTGTTTCC[C/T]TATCCTAATTAAGGA	10529
rs535779660	snp	C/T	0.00914312	0.0669923	intron-variant	NEBL	GRCh38.p7	10:21094284	GAGGTGGGCGGATCA[C/T]GAGGTCAGGAGATCG	10529
rs535791894	snp	C/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21032997	AATTATGGTGTAAAA[C/G]GTGAGAAATTAATAC	10529
rs535797191	snp	G/T	0.000798403	0.0199641	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21135141	CTATTTCATCCCAGA[G/T]CTCAAGCTGAGAGGA	10529
rs535799444	snp	A/G	0.00119737	0.0244387	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21127512	ACTATGTCTCTCCCA[A/G]TGAGATATACTGGAA	10529
rs535799903	snp	G/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20845946	TTTGATATGAATGAA[G/T]TTGTGCTGTGAGGAG	10529
rs535809800	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20812394	TGTTACATACGTATA[C/T]ATGTGCCACGTTGGT	10529
rs535812924	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20949825	CTTAATTTTTTGTGG[C/T]ATTTTCTGGAATACT	10529
rs535820234	snp	C/G	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:21120259	ATGTGCCTATATCCC[C/G]AGCTACTCTGGAGGC	10529
rs535827240	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21083067	GCACTTGACCTGAAT[G/T]CACCCTTTCTTTGGT	10529
rs535840918	in-del	-/C	0.0138799	0.0821421	intron-variant, upstream-variant-2KB	NEBL, NEBL-AS1	GRCh38.p7	10:21173450	CGGCTCGCCGAAGTG[-/C]CCCCCTGGGTGCCCA	10529
rs535842164	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21093895	AAAGTTCTCACTGAC[C/T]TTCTTTTCTACAGAG	10529
rs535842498	snp	C/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21048991	CTCCAGCCTGGATGA[C/G]AGAGAGAGACTCCAA	10529
rs535854674	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20917130	ATCCATGTGTGCCTA[A/G]CACAAAGCTGGTAAG	10529
rs535866912	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20943987	TCTGGTCTGTTTAAT[A/G]AACAAGAGGCGGTTA	10529
rs535877848	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20990437	TATAAAACCACAGCA[C/T]TAGCTCTCTCTCTCT	10529
rs535881526	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21155582	ATACATAAGTACTTC[A/G]GAAATCTTGAGTACT	10529
rs535894270	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21100246	GGGATGTGTGGTACC[C/T]GACCATTCCCCACCA	10529
rs535896558	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21002758	GAGAACTCACTTACC[A/G]TCACGAGAACAACAA	10529
rs535899307	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20913624	ATATCGTATCAGGAA[C/T]TGTTAAATTTTATCA	10529
rs535917874	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20906919	ATCTACTTCATACTA[C/T]GCACTACAATGAGAC	10529
rs535921224	snp	A/T	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21144472	GGCTCACGCCTGTAA[A/T]CCCAGCACTTTGGGA	10529
rs535927510	snp	C/T	0.000708536	0.0188087	intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20835616	TCCAGGTCTTTCTTG[C/T]ATTCTTTCTGCAAAA	10529
rs535928504	snp	A/G	1.65466e-05	0.00287628	intron-variant, synonymous-codon, nc-transcript-variant	NEBL	GRCh38.p7	10:20831202	ATGACCAACCTGGCT[A/G]TAGATTTCAGATGTC	10529
rs535937383	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20872336	GCCACACAGAAAAAA[A/G]CTTCCGCGCCTGATC	10529
rs535940125	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21097204	ACGCCTGTAATCCCA[A/G]CACTTTGGGAGGTCC	10529
rs535958922	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21056381	GAGTTACTAAATTTG[C/T]GCAAAGTTCCCTGTT	10529
rs535963168	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20790549	GAGGTTGCAATGAAC[C/T]GAGATCATGCCACTG	10529
rs535963905	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21120200	GGCAATATAGGGAGA[C/T]CCTGTCTCTACCAAA	10529
rs535964504	in-del	-/C	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20994584	CATTAAGGGCATTGA[-/C]CCCCCCCGTACACTC	10529
rs535972429	snp	A/G	0	0	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20783514	TCTGGTTTTGAAATC[A/G]GTGGATGAAATTACT	10529
rs535991146	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20889068	TGTTTCGCATTAGCA[A/G]AAATAATCCCAAGGA	10529
rs535994632	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20908960	TTTTGTACTGATCAC[C/T]AGACACTGAGATCAT	10529
rs535999878	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21103568	CATCCTAACAAAAGT[A/G]GTTTTACTTTGTATC	10529
rs536008506	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20920044	AATGGTCCTTAGTGT[A/G]AGAGAGGACGCCCAA	10529
rs536015938	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21150591	TTGGCAAATATAAAA[A/G]TGAGATGTGAAAACT	10529
rs536030362	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21016122	TTTGAAGCAGTTCAT[G/T]CTGGGATGTGTGATC	10529
rs536031263	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20866010	AGTGTCACCATGTTA[A/G]CCTTCCCTAAGTGTT	10529
rs536031882	in-del	-/TT	0.0123036	0.0774623	intron-variant	NEBL	GRCh38.p7	10:21103044	CATGGCACACATATG[-/TT]TTTATTTCTCTTCGA	10529
rs536033057	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21025007	TTCCTAAAAAATTGT[A/C]TTGAATAGAAATCTT	10529
rs536038349	snp	A/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20848241	ATAAAATACTTTATA[A/T]ACTTTATACAGTGTT	10529
rs536045501	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20910276	TTATCATGGCTCTGA[A/C]AATTCTTTATAGTAT	10529
rs536045504	snp	A/G	0.00517822	0.0506191	intron-variant	NEBL	GRCh38.p7	10:20982167	AACAGCGGGTACTCA[A/G]AAATCATTTGCATAT	10529
rs536049291	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20859890	ACATATGATTTTCAC[A/G]TAGATAAAATAAAAG	10529
rs536055128	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20984753	GCCACGGACTGGTAC[C/T]GGTCCATGGCCTGCT	10529
rs536060328	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20940001	GGAGACTTTAACAAC[C/T]CACTGTCAATATTAG	10529
rs536075054	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21022118	TACTCACTGCTCCCA[C/T]GTTCGGCTGGCGCTG	10529
rs536092056	snp	C/T	0.00636936	0.0560724	intron-variant	NEBL	GRCh38.p7	10:20942280	AGCCCTCAGAAATAA[C/T]GCCGCATATCTACAA	10529
rs536103998	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21107906	TCTTGGGAGGGTGTA[C/T]GTGTCCAGGAATTTA	10529
rs536108878	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20977164	TACCTTCCAAAGGCC[A/G]ACCTCCATTTCACTG	10529
rs536108988	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20970199	GGATGGGAAGCCCAG[C/T]GGATAAGCTGTAAGA	10529
rs536112371	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20972988	TCACGTCTTCCATAA[A/G]AAAGAAACTATTAAA	10529
rs536113682	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20901138	GGCATGAAAAGGTCT[C/T]CTCATTCTCTGTGCC	10529
rs536120599	snp	G/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20903281	GCTCAATATCACTAA[G/T]CATCAGATAAATGCA	10529
rs536121436	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20895212	TAGTCCTGATGGTTT[A/G]TGTAACACAAGTTAG	10529
rs536132666	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21094263	ATCCCAGCACTTTGG[A/G]AGGCCGAGGTGGGCG	10529
rs536135928	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21163007	CATTATTAGATTGGA[C/T]ATTCCAATGAATCCT	10529
rs536136107	snp	C/T			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21132366	TATAGATGTGCCATA[C/T]TTTGTTTATCTACTC	10529
rs536140187	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20932275	TCCTTTGCAGGGACA[C/T]GGATGAAGCTGGAAG	10529
rs536150817	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20895716	TCACATGTCAAGTAT[A/G]TGGGAAAGGGTATGA	10529
rs536160175	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20890098	GCCAAGTTAAATAAA[C/T]GGCTATCCAGCACAG	10529
rs536164791	snp	C/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21113707	CCTTTCCTTGGTTTT[C/T]AGTTTGTATGGAATG	10529
rs536177823	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21036315	TCAAATTAGCCAGGC[A/G]TGCTGGTGTACACCT	10529
rs536179587	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20854268	TATTTGAAAGGGAGC[A/G]GGAAAGAGCTGGCCA	10529
rs536182681	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21060105	TAAAAAATAGCAGCT[A/G]GAGATGCAGCCAGAT	10529
rs536184315	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21162699	ATGGGAAGACAAACA[C/T]GACCATCATACAAAG	10529
rs536185012	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20856884	CTCTTGCCTAGGCTG[G/T]AGCACATTGGTGCCA	10529
rs536195117	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21074520	AGTCTCGCTCTGTTG[C/T]CCAGGCTGGAGTGCA	10529
rs536206120	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20932751	TTGTCGATACTAATC[A/G]TTGTGCTATTTCTTC	10529
rs536216875	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20837793	AATGCTCATTTACCA[C/T]TCTGGAAATCCTAGG	10529
rs536220166	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NEBL, NEBL-AS1	GRCh38.p7	10:21173629	CGTCTTCGTTCGCGC[A/G]CCCTCCCCCCGTGCC	10529
rs536231198	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21113032	CCTGAAGAAGAAGGA[A/G]GAGGAGAGGGAGGGG	10529
rs536236424	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20959643	ACAGCCTCCCTTCTT[G/T]AAGAGTTGTTCCCTA	10529
rs536239965	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21120185	AACCAGCCTGGCCTG[A/G]GCAATATAGGGAGAC	10529
rs536251012	snp	A/G	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20997411	GAAGTGGCCACAGTC[A/G]CCATTAGGTACCCCC	10529
rs536262432	snp	A/G	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:21090655	CTTATCCAACTCACT[A/G]ACCTGTGTCACACAA	10529
rs536262768	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20851247	TCATTCAGAAATGTG[C/T]TCTTGATAAAATTTA	10529
rs536275971	snp	C/T	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21126540	TTAGCATACACCATC[C/T]TTTTTTCTGGAAGGG	10529
rs536279190	snp	C/G	0.000798403	0.0199641	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21135851	GCTGGAAATCCAGCT[C/G]TTCCTCCTCAAACCC	10529
rs536292584	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20967891	TATTTTCAAAGAAAG[C/T]AGGGACGCAGTTTTA	10529
rs536303461	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20804282	TACCATCTGAGCACT[A/G]GACATTCAATTCAAA	10529
rs536304619	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20832768	GTGGTAAACAAAAAT[C/T]TCAGTCTTGGAGTAT	10529
rs536310731	snp	A/C	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	NEBL, NEBL-AS1	GRCh38.p7	10:21172235	TCGTCAACAAAGTAC[A/C]TGGCCCCAGAGTCTG	10529
rs536314508	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20792032	GTGCAGTGAAGCCAC[A/T]GTTAAGGTTTCAAGT	10529
rs536318308	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20917413	ACTGATATACCCATT[A/G]GCGTCACAACAGAAG	10529
rs536319368	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20938005	CTCTGTAGACTCCAC[C/T]TCTCGGGGCAGGGCA	10529
rs536320666	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21158122	ACAGCAAGCCTAGCA[A/T]ACTATGACAGAACCT	10529
rs536335183	snp	C/T			upstream-variant-2KB	NEBL	GRCh38.p7	10:21175435	ATTCCGTTGCTAGCG[C/T]ACAGATTAAGACTCA	10529
rs536337513	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20927246	CCGCAGATGCCCACA[A/G]AACATCATAGCCGAC	10529
rs536357698	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20947337	AGGTACTTTGTCTGA[C/T]ATCCTCATATCCTCA	10529
rs536373810	snp	A/C	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20921202	TAGTGCTGATCCATG[A/C]CAAATTTTTCAGCTC	10529
rs536377105	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21089479	AGAAGGGGAGCAAGA[A/G]CACGTAGCCAAAGAG	10529
rs536389772	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20907427	ATATTCACCCTCTAA[C/T]TTTCTGTCTGATACA	10529
rs536395534	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20952271	GTAAAACCCCGTCTC[C/T]ACTAAAAATATAAAA	10529
rs536400111	snp	G/T	0.00072999	0.0190909	intron-variant, synonymous-codon, nc-transcript-variant	NEBL	GRCh38.p7	10:20897179	TTCAGTTTCATCTTT[G/T]ATATCCTCAAATACA	10529
rs536413727	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20953927	CGATCTTGCATTGAA[A/G]GGGTAGACTCATTCC	10529
rs536418336	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21053557	GTTTTCATTTTTCAA[C/G]TATAAAAATAAGCCT	10529
rs536422933	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20989033	AACTAAATATTATCA[A/G]TATGAATTTACAGTA	10529
rs536425907	snp	A/C/G	0.00279242	0.0372774	intron-variant	NEBL	GRCh38.p7	10:20963110	TTCTCTCTGTACTTT[A/C/G]GATTTGTAAAAGCAC	10529
rs536434368	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20786247	TAATATGTGATTTCA[C/T]ATTCTTCAGAGAACA	10529
rs536435791	in-del	-/C	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21119799	TGGACCAAGAAATGT[-/C]CTTGATAGCTATTTC	10529
rs536439209	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20829979	ACTCTTCTCCACTGA[C/T]TCAAATGTCTATTTG	10529
rs536439896	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21088985	ACAGGTGAAGCTCTA[G/T]AGGGGAGATGGGTGA	10529
rs536445889	snp	C/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20978692	CCCAGGAGTTTGAGG[C/T]TGCAGTGAGCCGTGA	10529
rs536449067	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	C10orf113, NEBL	GRCh38.p7	10:21147636	CCTTGATATTTACCA[C/T]GGTTCAAGCCTACAT	10529
rs536450220	snp	A/G			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20883317	ATTTGGTTGGTTACC[A/G]AATCAGAAGCAGCAC	10529
rs536451817	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21153736	GGTCAGGCTGGTCTC[A/G]AACTCCTGACCTCGT	10529
rs536469972	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20820290	TAGCTGGGGATCTAA[C/T]TCCATTGTTTGTGGT	10529
rs536472148	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21066452	GAAGTAAACAAAATG[C/T]AGTGAGTACACAAGA	10529
rs536484551	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20991815	TTATTCCCATCTTTG[C/T]GTCCATATGTACTCA	10529
rs536494860	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20786798	CAAGATTTCCAATGG[A/G]GGATTTGAAGATATA	10529
rs536497302	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21102152	CAGACTTCTACCACA[A/G]CTGTTAATAAGCTAC	10529
rs536509209	snp	A/T	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20780178	GGAGAAAAGCAATTG[A/T]GTTCTGTGATAAATG	10529
rs536525930	snp	C/T	0.00517822	0.0506191	upstream-variant-2KB, intron-variant	C10orf113, NEBL	GRCh38.p7	10:21146858	TTTTCATAATCAATT[C/T]GGACACAATTATCTG	10529
rs536528022	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20833742	GCCTGGGCGACAGAG[C/T]GAGACTCCGTCTCAA	10529
rs536530442	in-del	-/TCTT	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:20911439	CACATTTTAAAACTC[-/TCTT]TGTATTATGATTACA	10529
rs536532088	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20924297	CTGTGTCTTCTGAGA[A/C]CCTGAAAGTTTCACC	10529
rs536537881	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20949005	ATATGTCACATGTGC[A/G]AAGACAGCTATTTCA	10529
rs536539130	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21153190	ATTCAATATTATCTC[C/T]CATTTCACAGATAAT	10529
rs536553546	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20898573	ACAAAAGATTCTGGG[A/G]GAAAAAAGCAGGTTT	10529
rs536566612	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20788186	TGTGAATGTGTTTAA[A/G]TTATCTGTGACCAGA	10529
rs536575862	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20858143	AGGAGTGAGGCACAG[A/G]CCTTCTAAGGAAGCA	10529
rs536583077	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20980211	GTGTTGGAGTTGGTA[C/T]CACCTATAAAACTCA	10529
rs536590558	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:20997786	ATGCTTGAGATAGGA[A/T]CCTATACAGAATTTG	10529
rs536592198	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21072035	GTTGGCCAGGCTGGT[C/G]TTTAACTCCTGACTT	10529
rs536595394	in-del	-/GA	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21100927	TGTAACAGTTTTTGT[-/GA]TTCTTTGTTTGTTTT	10529
rs536608452	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:20944316	GAAGCAGGAGAATCA[C/G]GTGAACCTGGGAGGC	10529
rs536623906	snp	A/T	0.000798403	0.0199641	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21140960	ACTTAAAGTAAAATT[A/T]AAAAAAAAAGCTAAT	10529
rs536631497	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20967454	CCAACATGGCCAAAC[C/T]CTAGCTGTACTCAAA	10529
rs536633789	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21035939	AGGCTGAGGTGAGCG[A/G]ATCACTTGAGGTCAA	10529
rs536637070	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20970146	CTGTGTTCCAAGCAT[A/G]GTAATGAGTGTTTTA	10529
rs536641502	snp	C/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20808787	TAACTCAAAATCTCA[C/G]CGCTAGGCACCTATT	10529
rs536661283	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20966995	GACCATACCATTCAC[A/G]TTAAAGGAGATTCAC	10529
rs536665778	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21003914	ACCCTTTCAGTTCTT[A/G]TCTCTATTATGGAAC	10529
rs536672796	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21060605	TATCTCATTTTTTTT[A/T]AAAATCCCCTGGAAC	10529
rs536675432	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20922220	CTGTGACTCTGGCTG[A/G]GAATTAAATGATTCT	10529
rs536688569	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21041438	ATCATCACCACTAAC[A/G]ACCAAGGGAAGATGC	10529
rs536699105	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21016004	GCCCCCGCAGGTGAA[C/T]TATAATGTTGCTGAT	10529
rs536726535	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21004335	GAAAAATTTATTAAA[A/G]GAGTAAAATTTTGGA	10529
rs536738587	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20923100	ATGAGACAGGGTCTC[A/G]CTCTGTCACCCAGGC	10529
rs536741121	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20968031	CAAAGACTTGGGTTT[C/T]TTCGTAAATGGCAGG	10529
rs536746485	snp	A/T	0.00279162	0.0372561	upstream-variant-2KB, intron-variant	C10orf113, NEBL	GRCh38.p7	10:21147399	GTTTCTCCTCCGGTT[A/T]TTTTTTTTTTTTTTT	10529
rs536760568	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20884506	ATGCAAATTAAAATA[A/G]TGGCTTTGCCTCTGA	10529
rs536763378	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21036743	TACCCCAGGTACAGA[C/T]TTAAGCTTGTCTCTA	10529
rs536769168	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20914481	GAAGCAAACATTCCT[A/T]ATACAATATTTATCA	10529
rs536769784	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20956249	TAGAAATACTTTTCC[C/T]GAGGAGCGGTTGTTC	10529
rs536776615	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20881438	AGGGAAATGGACCAG[C/T]GCCATCCATTACCAC	10529
rs536779718	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21153065	CATCACGAGCCTTCT[A/G]GCTCACAAATGTGCA	10529
rs536784435	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	C10orf113, NEBL	GRCh38.p7	10:21147027	ATTTCTGAAGGGCCT[C/G]AGGCTTCTAGTGACT	10529
rs536785960	snp	C/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20841807	TTGGTTCTGTTTTCT[C/G]TATTGGCTTTGCTTT	10529
rs536790568	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20848816	CCACTGAATAAGACA[C/T]AAAAAATACAAGTAA	10529
rs536793084	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20998837	ATTCGATCACTTTGT[G/T]TGTCTATGGACTAAC	10529
rs536810177	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21165892	ACTTTCAGTGCTCTC[A/T]GATGTATGGAGCATT	10529
rs536815646	snp	C/T			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21136445	GCGATCCTCTCACCT[C/T]AGCCTCCCAAAGGGC	10529
rs536827255	snp	C/T	0	0	intron-variant	NEBL	GRCh38.p7	10:20832961	TTCAAAGCCCCAAAA[C/T]GAAATGTTTCATTTG	10529
rs536828139	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21113640	GCCCAGGTCCCATTG[C/T]CCAGAATGTGTTGTC	10529
rs536851822	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20915060	CACCCACCTCAGCCT[C/T]CCAGAGTGCTGAGAT	10529
rs536862979	snp	A/T	0	0	intron-variant	NEBL	GRCh38.p7	10:20995129	TGAAGCAAAGTCTGA[A/T]CGTCAGGACAGGGAA	10529
rs536865290	snp	C/G	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:21031307	CCCAGGAAGAGAAAG[C/G]CCAGAGCTGCAGAAG	10529
rs536870760	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21159177	ACTTTTTCAATCAGG[A/G]TTTTATTTTTCAAAG	10529
rs536878408	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20948408	CCTTTCCTTTTATAA[A/T]TACCAAAAAATATTA	10529
rs536879621	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:20970767	CATTTCACAGATGAA[C/G]GAAGTTTGCAGAAGT	10529
rs536886160	snp	C/T	0.0023933	0.0345097	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21132426	ACTTTTTAGCTGTTA[C/T]GCATAATGCTTCTGT	10529
rs536886928	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21053184	TAAAATAAAAAAATT[A/G]AAAGAATTCACTGAC	10529
rs536897837	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20908492	CAGGCCATAATGAAA[A/G]CATTATGAGGATCCT	10529
rs536903404	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21035896	GGCTGGGCACGGTAG[C/T]TTAGGCCTGTAATCC	10529
rs536911870	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20991951	AGGACAAGACTGTAT[C/T]CTTTTTTATGGCTGT	10529
rs536917187	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20988780	TGTCCCACCACACCA[C/T]GGAAACCACACTTGG	10529
rs536921823	snp	C/T	0.00119737	0.0244387	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21139464	ATAAGGATATCAACC[C/T]AGGAGACCAAGGTTG	10529
rs536925286	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20985581	AATATCCGACAAACC[A/G]GTCACATTGCTCCTT	10529
rs536941815	snp	C/G	0.0166325	0.0896639	intron-variant	NEBL	GRCh38.p7	10:20942974	GGAGAAATAGGAACA[C/G]TTTTACACTGTTGGT	10529
rs536949247	snp	A/G	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21139125	AGCTCTCAGATGTTA[A/G]GAGTCACGGCTGGCC	10529
rs536962783	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21063997	GGATTGCTTGAGCCC[A/G]GGAGGCAGAGGTTGC	10529
rs536963492	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21041267	TGTGTCCATGTGTAT[C/T]CAATGGTTAGCTCCC	10529
rs536966620	snp	C/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21101497	TGTGAAACATCTGGA[C/G]AAAGGCAAGACCTAG	10529
rs536970154	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21119335	ATACCCTTCATCTAG[A/T]TTCACCAATCACCAA	10529
rs536985734	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21083642	TTGAGCTCAGGAGTT[C/T]GAGAACAGCCTGGGC	10529
rs536989634	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20827577	TTTTTACAATTTTAG[A/G]ACAGAAGTCAAGTTT	10529
rs536999529	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20811792	TGGCATATACCAAAA[A/G]TATTCTTTAAGCTAC	10529
rs537004821	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20818098	TCTCCCTTCAATAGA[A/C]GCTAAAGCTCTCTGA	10529
rs537010034	snp	C/G	0.000798403	0.0199641	intron-variant, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20873465	GCAGAGAACAAACAA[C/G]GAGGAGGAAGAACAG	10529
rs537013669	snp	A/T	0.00557542	0.0525036	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20866930	CATGGTAAGAACAAC[A/T]TTGGACCCAAATCTT	10529
rs537017665	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20797178	CCTCAGTGAATACTA[C/T]TGTCCATGTTGTATA	10529
rs537026268	snp	C/T			utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20785187	ACAAGGAAATTTCTC[C/T]GTTTAGTAGAAGTTT	10529
rs537027952	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20901273	AGCTTGATGTTTACA[C/T]GTAAGCAAATGTATT	10529
rs537037056	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21096307	CTAATTCCCCTTGTT[A/G]GATATACATGGAATA	10529
rs537053489	snp	C/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20858459	TGGTAAATGGACAGA[C/T]GAATTTACAAGGAGC	10529
rs537054062	snp	G/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21089382	GCCATGGAAGTCCTG[G/T]ACTCCAAGACTGCGT	10529
rs537056146	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20860005	TCTTTAATAAAAAAA[A/C]CTCTGCTTCTACATT	10529
rs537072235	snp	G/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21012990	GTCGAAAACCTAGCA[G/T]TGCACAAAAATCAAA	10529
rs537094001	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20791639	GTCTCAAGCAATTAT[C/T]TTGTCTCAGACTCCC	10529
rs537094265	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20784932	TTCAATAATAGGAAC[A/G]CGCAGTGCAGCTGCC	10529
rs537101081	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20810789	CAAAAACAATTAATT[C/T]GTAAAATGGAACTGG	10529
rs537106859	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20970636	CCTGGAAAACAGAGC[A/G]AGACCTCATCTTAAA	10529
rs537127341	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21171083	GCTCACGCCGGTAAT[G/T]CCAGCACCTTGGGAG	10529
rs537127662	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20899849	TTGCTGGATGAAGTC[C/T]TTAATGGATCGTTTG	10529
rs537138323	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21060196	TACAGCTGATTAAGC[C/T]TCTCAGTGTAAAGCA	10529
rs537144572	in-del	-/TGTC	0.0119091	0.0762411	intron-variant	NEBL	GRCh38.p7	10:20921018	TCTGTCCACTGAAAA[-/TGTC]TGGAGTAATGACAGT	10529
rs537149363	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20896711	TGATTTCATGCCAGC[A/G]TGACAGCAAAACTCA	10529
rs537159741	snp	G/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21090738	CCCTATCGCCACCTG[G/T]TTTTGTCATTAGCCA	10529
rs537167608	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20978103	CTGCAGAAGAAAATA[A/G]GGAAATAGATATGAA	10529
rs537168571	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21102309	TGCATATATTTAGAG[C/T]GCACAACTTAATGGA	10529
rs537177918	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21094894	CCTCTCGTCATAGTT[A/T]CCCAGGTGATGGTGA	10529
rs537178882	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20923619	GGGAGGTGGAAATTG[A/C]AGTGAGCCGAAATCA	10529
rs537191778	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21001176	CTCTATTGCCTGCTT[A/C]CCCAGGTCCAGCCAG	10529
rs537201378	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	NEBL, LOC102725112	GRCh38.p7	10:20885023	ACTTTATCATTCTAG[C/T]TTGAATTTAAGCATC	10529
rs537206521	snp	A/G	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21007549	TTTCTATTTCATTTC[A/G]TACATTATCACCCTT	10529
rs537215864	snp	A/C	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20835876	CATGTGAAAATCTTC[A/C]CTGACAATTTTCTTT	10529
rs537227164	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20842253	TGAGTCAAATGACCC[A/G]AGTGAAAGTCAGACC	10529
rs537234173	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20807007	AGGACACTGAGGGCA[C/T]AAATCAGTGACCCCA	10529
rs537236731	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21094375	GGTGCAGTGGCAGGC[A/G]CCTGTAGTCCCAGCT	10529
rs537237467	snp	C/T	0.0225045	0.103662	intron-variant	NEBL	GRCh38.p7	10:20786628	AGCAATTCAAGTTAC[C/T]GGACAGTGTAGAAGA	10529
rs537238723	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21101428	GTAGTAGTTTTCACT[C/G]CTCCTTCTGCTACCC	10529
rs537255498	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21152343	CCCAAGAATTCCAAA[G/T]GCATCCAATGAGCAT	10529
rs537256339	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20814324	AACCTGCGCAAGCCC[A/G]AGGACTCGTATCTGT	10529
rs537273154	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20944478	ACACCCCACATTGCA[A/G]ACATTTTAGGTTAAC	10529
rs537283679	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20885784	GGTTGTAATTATCTG[C/T]TTTTTAAAGTGACCC	10529
rs537296215	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21066906	TCATGTTCAGTTGCT[C/G]CATCTCATAGAATAC	10529
rs537302220	snp	A/C	0.0189856	0.0955633	intron-variant	NEBL	GRCh38.p7	10:21106663	AGGATTATCTTGGCT[A/C]TGTGGGCTCTTTTTT	10529
rs537302753	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21100997	AACATTTTGTGGCTT[C/T]TTTTGGAAGGAAATA	10529
rs537312715	in-del	-/AAAC	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:20966702	AGGAAGACTTCTGAA[-/AAAC]AAAATAACAGGCAGA	10529
rs537317346	snp	A/G			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20860076	TGAGAATTATGCACT[A/G]AAATACCAACATTTT	10529
rs537320316	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20796574	AAATTAGTCTGCAAA[C/T]GTTCTGACAGAACTG	10529
rs537322901	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20904003	CTTGTACCCCCAAAA[A/C]CCATCGAAATAAAAA	10529
rs537337069	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20836396	TCCAGCTAATTTTTG[C/T]ATTTTTAGTAGAGAC	10529
rs537367770	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21035400	AAGCATTGTGTACAA[C/T]CTTGTCAACTACTGT	10529
rs537377736	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21012988	GGGTCGAAAACCTAG[C/T]AGTGCACAAAAATCA	10529
rs537378621	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20919165	GGCAAGAGAAGGCAT[C/T]TGAGCTATAGTTAAG	10529
rs537386174	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20833402	ACTATGGCAAAGTCC[C/T]GAACATTGGTTGAAA	10529
rs537388453	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20996690	ACTGTAATGTGAAGC[C/T]ATTAAACTGCAAAAG	10529
rs537397411	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21002967	TGAACCCATCATGAT[A/G]GGTTTAATAACATCA	10529
rs537397734	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20924972	GCAGACCCCCAACCC[A/C]CTGCTCTATACCACC	10529
rs537404695	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20830461	CCATAAATTTTTGTG[A/G]TCACTACTTCTCCCA	10529
rs537412682	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20948294	TTTCATGCCTTTCAA[C/T]CAATAACATAAAGCC	10529
rs537426764	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20908452	GAAAACAAGCCCCCA[C/T]GGGCGTTAGAAGCAA	10529
rs537427780	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20946167	CTAAATGAGGACAAC[A/G]AAGGTGAGAGGCAGC	10529
rs537427789	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21089129	TGGGAATTAAAGAAG[A/C]AGCAGTGAAAGAGGA	10529
rs537430154	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20874772	GAAGATGAAGTCTTG[C/T]TATGTCACCCAGGCT	10529
rs537432190	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20793403	GGACAGGAGATTAAG[A/G]ACTGAGGACAGAGGA	10529
rs537434931	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21040773	CATTAGAGCTGATTG[C/G]ATCATGGGGGGATTT	10529
rs537440902	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21064215	AAATATAGAGTTAAC[A/G]TCAAAAAAATTGAAT	10529
rs537448855	snp	C/T	0.00318978	0.0398085	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20870101	GGAGGCCTAGGTGGG[C/T]GGATCACTTGAGGTC	10529
rs537461895	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21171589	AATTTCATTACCCGC[C/T]ACATGGGGGTAATAA	10529
rs537463182	in-del	-/AAAAA			intron-variant	NEBL	GRCh38.p7	10:21094528	AAAAAAAAAAAAAAA[-/AAAAA]TTAGCCAGATGTGGT	10529
rs537469339	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:20917277	CTGTCCTCTAACAAT[C/G]ACTAATATTGTATTT	10529
rs537476654	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20940966	ACCAACCAAAAAAAG[C/T]CCAGGACCAGATGGA	10529
rs537484740	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21046435	TTACATAGTGTACAC[A/G]TGTATCAAAACATCA	10529
rs537485281	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:21122074	TCTATCACCCAGACT[C/G]GAATGCAGTGGCACG	10529
rs537493635	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21122391	CCACTAAGTCAAAAC[G/T]CTACCATCTGTGTCT	10529
rs537496638	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20793890	TGAGCAGCCACAATG[C/T]GGACCTACCGAACTG	10529
rs537499544	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21170980	AGCCAAAAGGCCAGG[A/G]GTCCAAAGGCCCCTT	10529
rs537500323	snp	C/G	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21125611	AACGCAATGAATTTA[C/G]AGGGAATGTAAGTTT	10529
rs537507197	snp	A/C	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20788089	TTCCTGTTTTGAAGA[A/C]CTCGGAATTCTAGAG	10529
rs537507365	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20954552	TGAAAATTCAGGCTC[A/G]CAGACAATTTGAATG	10529
rs537507946	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21086339	TCAATTGTGCTAAGA[C/T]CCTATAACTCAAACA	10529
rs537518616	snp	C/G	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:20901746	CATTTTTTGTTGCCT[C/G]GTTTTTGTTTTGATG	10529
rs537521119	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20903766	GAAGTAACTCAGGAA[A/T]GAAAAACCAAATACT	10529
rs537536043	in-del	-/AAATGTG	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20886839	ACTATTATTAACCTA[-/AAATGTG]AAATGAAGAATACAA	10529
rs537539356	snp	C/T	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21132381	CTTTGTTTATCTACT[C/T]GTCAATTAGTGGACA	10529
rs537542952	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21023352	GCAGGTTCACTCAGT[G/T]TGGGGGCATGCTTTG	10529
rs537549394	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21020512	ACCCTTCCAGCATGT[A/G]TGCCAAATCATCCAT	10529
rs537555103	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21076847	GGCAAAGGACTTGAA[C/T]GGATATTTCTCCAAA	10529
rs537572907	in-del	-/AA			intron-variant	NEBL	GRCh38.p7	10:20954042	AAAAAAAAAAAAAAA[-/AA]GAAAGAAAAAACACC	10529
rs537585943	snp	A/G	1.64765e-05	0.00287019	intron-variant, nc-transcript-variant	NEBL	GRCh38.p7	10:20819404	TTGAGAAAATATAAA[A/G]GGAAACAGAAACGAC	10529
rs537595091	snp	A/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20860019	AACTCTGCTTCTACA[A/T]TGATCACAAATGCAA	10529
rs537604543	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20816435	CCTTTAAAAAGCCAG[C/T]ATGCTTCTCACTGGT	10529
rs537605293	snp	G/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21052698	ATCACCAACACTCAG[G/T]AAGAGCAGTGCCGCT	10529
rs537605879	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21016997	ATCAACCCTTGTATT[A/G]CAATTCTTTGCTTAC	10529
rs537608892	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21010329	AGCTCACTACAACCT[C/T]GACCTTCTGGGCTCA	10529
rs537615029	snp	C/T	0.000798403	0.0199641	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21139392	AGCAGGAGGGGAAAT[C/T]GGTTACAATTTGGAT	10529
rs537618860	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21021765	CACAGTACAACGAAA[G/T]TTCTGTGGTAGCAAT	10529
rs537632706	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20972436	CAGCAAAAGAGAAAA[A/G]GAAATACAAATTTAA	10529
rs537635699	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21002546	AAAGAACTGAGACGG[G/T]GTAATTTATAAAGAC	10529
rs537640411	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20974951	TGCTTCAGTTCATCT[A/G]TTATCTTGATTGTAT	10529
rs537643938	snp	A/T	0.0134861	0.0810011	intron-variant	NEBL	GRCh38.p7	10:21091520	CTTTATCCAATTAGC[A/T]ATCAGTACCTCAAGT	10529
rs537648950	snp	C/T	0.000798403	0.0199641	intron-variant, nc-transcript-variant	NEBL	GRCh38.p7	10:20813870	GGATTAATAGTGAAG[C/T]AATGCCATCCGTGCA	10529
rs537649573	snp	A/G	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21146099	GAAAAATTCATTTGA[A/G]TCTTCCTTTACAAAT	10529
rs537655095	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20931510	AAAGATATGGGATGA[C/G]AGTCAGTAGATCATC	10529
rs537657974	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20849497	CCTCATGAATGGATT[G/T]ATGCCAATATCATGG	10529
rs537660529	snp	C/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20874713	ACGAAATCTAGAGAG[C/T]TCTAACACAGCCTCC	10529
rs537661572	snp	C/T	9.89789e-05	0.00703418	intron-variant, missense, nc-transcript-variant	NEBL	GRCh38.p7	10:20888155	ATTGTGGCTGGCATC[C/T]GCTTATAAAGAGAAT	10529
rs537668298	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20816969	CATGCTGGTAGAAAA[A/G]GGAGGGAAAATGTTT	10529
rs537668379	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20809981	AGCCAGTACCCAAAA[C/G]AGTCAAGACAAAGTC	10529
rs537672455	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21010914	TCAACTTCCCTCAAA[C/T]CTATGTGACCTCCCA	10529
rs537683427	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21009398	GATTCCTGTAAATAA[A/G]AAAAATTCCACAGAA	10529
rs537691417	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20997578	TGCACTATGGATTAA[A/C]GTGTTCAACCAGTTC	10529
rs537695047	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20850130	AAAGTGTCAGTTATA[C/T]TATCATAGAAAATTA	10529
rs537697735	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21097993	TTCGTAATAATCTCC[C/T]TTTGAATCTTGATGT	10529
rs537708446	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20968589	CGTCGCATGTATCAC[A/G]ATAGACAAGTGCAGT	10529
rs537733396	snp	A/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20884214	ATGTACATTTATGTT[A/T]CACTTATAGATTTTT	10529
rs537734785	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21005027	TCAAGACCTCACCCA[A/G]ACAAATTCTTAGGTT	10529
rs537736355	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:20892998	GGAGGAGTAACCACA[G/T]AATTTAATGTTTTTG	10529
rs537737492	snp	A/G	0.00358779	0.0422022	intron-variant	NEBL	GRCh38.p7	10:21168809	ATCTCAGCACTTTGG[A/G]AGGCTGAGGCGGGTG	10529
rs537737640	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21063991	GAAGGAGGATTGCTT[C/G]AGCCCGGGAGGCAGA	10529
rs537742538	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20928056	TTGTCATTTCAACAC[A/G]TTATTGATATAAAAT	10529
rs537761955	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20886248	TGGGGAAAGGTAGGG[C/T]GCAATGGCTCACACC	10529
rs537762506	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, upstream-variant-2KB	NEBL	GRCh38.p7	10:20959112	AAAGGCAGCTAAGAA[A/G]GAGCCACACAATATT	10529
rs537764906	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21104388	ATCTCCCCATTTCAC[C/T]AGGCCTTATTTAATT	10529
rs537768025	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21106132	TTTTCTCCCATTCTG[C/T]AGGTTGCCTGTTCAC	10529
rs537768644	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21028714	TTACATAAATTCAAA[C/T]CCTAAAAAAGGGAAA	10529
rs537773387	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20888892	AAGACAAACAAACTA[C/T]GTTCTTCCATTATCT	10529
rs537788648	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20843377	CAATACAATACAGTG[C/T]TCTGAGCCCTTTCCT	10529
rs537791239	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20935572	ACTGTGCAATGAGAG[A/G]CTGATTCTGGAATCT	10529
rs537796107	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21005510	AAGGTCAAGATGGGG[A/G]GATCGCTTGAGCCCA	10529
rs537810371	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21067606	TGTAACTCCAAAAGG[C/T]AGAAAACAGACCATT	10529
rs537811034	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21122963	ACATATTTCCTTGTA[A/G]GCTGCTGGGGTCATA	10529
rs537813149	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20826913	AAGCCGTTATCACTG[A/C]ATTCAAAAAGAAAAT	10529
rs537817185	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20869524	CTCTAAAAGTATGAT[A/G]ACACTAACCACAGCC	10529
rs537826661	snp	C/T	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:20840208	AAAGCACAGTGACAC[C/T]ATATGACCCAAAGTA	10529
rs537842779	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20805428	ATGTTATACAACTTA[C/T]TGGTACATCTTGACT	10529
rs537852673	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21122674	CAGAGTTTGGGTTTG[A/G]AGATCTGAAGTTTAG	10529
rs537856927	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20800027	TAACAAAAATCTCTA[A/G]CATAATTTTATTAAC	10529
rs537857489	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21162122	ACTCTGGATACCAAA[G/T]ATTGGTGGAGATCCC	10529
rs537861141	snp	G/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20999909	CCCCATGCTGATGTT[G/T]GAGAAAAGATCATGT	10529
rs537862709	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21073671	TTACTGCTTTCTTTT[C/T]CCCACTGCTCCCTAC	10529
rs537864169	snp	A/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21168542	CTGGCTTTTAAAAAA[A/T]ACTGTAAAGAACATT	10529
rs537871999	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20942922	TAGAATGGCGATCAG[C/T]AAAAAGTCAGGAAAC	10529
rs537896697	snp	C/T	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21129071	ATTATCCTTCAGAAG[C/T]GAGGGAGAAATAGCA	10529
rs537896711	in-del	-/TA/TATATA	0.0287284	0.116357	intron-variant	NEBL	GRCh38.p7	10:20789853	TCTTATCTCAAATTT[-/TA/TATATA]TATATATATATATAC	10529
rs537899004	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20821975	AGATCTAACTCCAAC[A/G]TTACCCCTTCCCCAA	10529
rs537905331	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	NEBL	GRCh38.p7	10:21175985	TGAACTTTAAGTTAT[A/G]TTTAATCTTTTTTTT	10529
rs537909050	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20781085	GGTTAGTCCTTTGGG[A/C]AGCACGATGTTGCTC	10529
rs537911263	snp	C/T	0.00984648	0.0694715	intron-variant	NEBL	GRCh38.p7	10:21069970	GCGGCTTAGGGACTG[C/T]GCCCCTGGAGCCAGA	10529
rs537922239	snp	C/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20876279	TAAATCTATAGTTGA[C/T]AAAAGTTGTCTTATT	10529
rs537925828	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21072982	GGCAATAGACTATGA[C/G]TCTGTCTCAGAAAAA	10529
rs537929289	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20955138	AAGGGGTAGGGAGGG[C/T]CCTAAATTAGAGAGG	10529
rs537935527	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20938184	CCTAGCTGGGAGGCA[C/T]CCCCCAGTAGGGGCA	10529
rs537949541	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21050262	TTCTCACGGAAACTA[C/T]CTGATTTCTGTTGGC	10529
rs537956079	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21102204	GAAGTTAGGATTCTT[A/G]CCCAATGCACAATCT	10529
rs537965142	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20949760	TTTTTCTGCTGAGGA[C/T]GTCTTTATTTCCTTA	10529
rs537965849	snp	C/T	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:21089348	AAATATGAACATGAG[C/T]ATCATCAGCTTAGAG	10529
rs537989320	snp	A/C	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20825021	TTCATCCACTCTCAT[A/C]CACACCTTAAGCCTA	10529
rs537992329	snp	C/T	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21136287	AGAAAGCCCCAAATA[C/T]AACTGGCGACTGTTG	10529
rs537995914	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20938463	TCATCAAAGACCAAA[A/G]GTAGATAAAACCACA	10529
rs537997769	in-del	-/TTG	0.00547608	0.0520389	intron-variant	NEBL	GRCh38.p7	10:21074798	ATATATATATTTTTG[-/TTG]TTGTTGTTGTTGTTG	10529
rs537998669	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20828106	GTGCTGATGCAATTC[C/T]TCTTCCTCAAAATAA	10529
rs537998721	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20834830	GGTGTAGAGAAAGTT[A/C]TAGGGTATTTCCTTT	10529
rs538004387	in-del	-/TAGA	0.0111196	0.0737302	intron-variant	NEBL	GRCh38.p7	10:21163811	TCTTCTGGCTCCTCC[-/TAGA]ATTCAATAAGAATGA	10529
rs538010888	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20828644	CTTTCTCTAAAAACA[A/T]AAACAGTTAATATAA	10529
rs538017649	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21056280	CCCTCTCTCTTGTTC[A/G]TAAAACCTAATATAG	10529
rs538021196	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21024206	ACATATAACAATGCT[C/T]TGTACTTTTTCCAAT	10529
rs538028464	snp	A/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20943928	GGGTCGTCTGTATCC[A/T]CTAAAATGACCTATG	10529
rs538030221	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21081446	GGTTTCTCATCATGG[C/T]TCCTAGTGGGAAAAC	10529
rs538032514	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20904841	CTTGGCTGTCAACAC[C/T]GTATCAAGAGCCAGA	10529
rs538034398	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21042787	ACCACAAGCTCTTAA[G/T]GCAACAATTTTCTCT	10529
rs538037571	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20905547	ACTGCCCCCATGATC[C/T]AATCACCTCCTTCCC	10529
rs538044113	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20893580	CTTGACCTGAAAAAC[A/G]GACATTTCTCTCTAT	10529
rs538053205	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20858122	CAATGAGTTAGTTAA[C/T]GAGGGAGGAGTGAGG	10529
rs538078100	snp	A/G	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21142806	CCAGTTGTGCTCCTT[A/G]TGAGAATCTAACTAA	10529
rs538078859	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20822939	CATCCTGCTCTCACC[C/T]TCCTACCTTTTGGAG	10529
rs538081173	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21062138	TAATTTTATCAGTCT[A/G]ACTTATATTTTATGT	10529
rs538084436	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21024926	CATCTAACACGAATC[A/G]GTAGCACCATACAAT	10529
rs538091623	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21078899	AGTTTGCTCCCAGAT[C/T]CAGGGGATGAGTGTA	10529
rs538113650	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21153552	TATTAATTTTGAGAC[A/G]GAGTCTCACTGTATC	10529
rs538114876	snp	C/G	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21142170	CATTCACTCTTGGTG[C/G]TATTCCTAATACACA	10529
rs538117233	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20783449	ACGTGAAGCTTAAAA[C/T]TTTAGGAGACTTATT	10529
rs538122399	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21149242	AGGGAAGCTCTGTAA[A/C]CCTTCCTCACCTTAC	10529
rs538137947	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20858699	GCTTTGTGGAGATCT[C/G]AGGATTTTGATGTTT	10529
rs538138163	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20965240	TTAATTACAATGCAA[A/G]AGATGAAAAACACAC	10529
rs538141775	snp	A/G	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21134552	AAGTCTTCTTCCAAG[A/G]ACTACCTTTTACACG	10529
rs538144527	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20939534	GCATCAACTAATGAG[C/T]AAAATAACCAACTAA	10529
rs538152241	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21048288	CTGAATACCAAATTC[C/T]TTCAAGGAGAGTCAC	10529
rs538169614	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20805037	GCAACAATGGAGGTA[A/G]GGCCAAGCACTCAGA	10529
rs538172140	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21026159	AAGATCTTCATGGAT[A/T]TATTTTCTGTAAAAC	10529
rs538180767	in-del	-/A	0.00199481	0.0315187	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20856100	AAGGAACACATTTTT[-/A]AGTCTTTCTCTCCCA	10529
rs538182839	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:20920613	CTTCTGTATTCAAAA[G/T]AAATAAAGACAAACA	10529
rs538186048	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20999323	CAAGCCAGGCTGGAT[G/T]CAGTGGCTCACGCCT	10529
rs538198605	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21156870	GCCAAGGTCACAATC[A/T]TGAGTTTTTCCCCCT	10529
rs538205981	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21121675	ATGCTAGGCTCACAA[C/T]TTCAGTATCTGAAAT	10529
rs538208978	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21001741	ATCGCCAAGGTCTGA[C/T]TGCAAAAATTCAAAA	10529
rs538228858	snp	C/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20826935	AAAGAAAATGACATT[C/T]TAGGCAACTTCTATG	10529
rs538233450	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21043452	TGAATGCTAAACTTT[A/C]TCATTTAAAAGGGAC	10529
rs538265718	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21085549	CTGAGGCTGGAGGAT[C/G]ATTTGAGCCCAAGAG	10529
rs538269263	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20925150	GTCACTGTTTATTAC[A/T]TTTCTTCCAGAAATA	10529
rs538274027	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:20894725	CGAGTCCATCCTAAC[G/T]AACACGGTGAAACCC	10529
rs538276681	snp	C/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20851546	TTTGGGAGGCCAAGG[C/T]GGGCAGATCACAAGA	10529
rs538281460	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21115384	GTTTCCATCTGGTAT[A/C]ATTTTCTTTCTGTCT	10529
rs538293102	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21037729	AAAAATGTGTGATTG[C/T]TGAAATAAAATAGTC	10529
rs538298445	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21049556	ACTATTGTTCTCCCA[A/C]CCATCTATTTATTGA	10529
rs538303391	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20800686	TGCATAAACGACAAA[A/T]GCTCACAATAAGAGA	10529
rs538313294	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	NEBL	GRCh38.p7	10:20817154	GGAGGCCAAGGTGGC[C/T]GGATTGCATGAGCTC	10529
rs538313509	snp	G/T	0.000798403	0.0199641	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20871060	GGCAATTAAAATATA[G/T]TCTATTAAAGTCATA	10529
rs538313844	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20794550	CCTTTTAATCGTTAA[A/G]TGTACAGTTGTTTGA	10529
rs538316858	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20843242	GGTAAGAGGGCCCTC[A/G]CTAAGAATCAAATCT	10529
rs538318793	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20803037	CAATGTCTCGTCCTC[C/T]AGTTCAGGGTTCCGG	10529
rs538319849	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20878100	TTAATTTTGGGGTGG[C/T]GCAAAAGACTACTGC	10529
rs538327778	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21153895	AAGATGTAGGACCTC[A/G]TTATATTTGTTAAAT	10529
rs538335165	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21152291	AGATTGGACCCCAAG[A/G]ACAGTGACGCCAGTG	10529
rs538336830	snp	C/T			utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20781416	TCAAGTTTCACACCA[C/T]GCCTGTAATAGACTT	10529
rs538337451	snp	A/G	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21135354	GGTACTTCCCCATCC[A/G]TATCCTCCAAAGGGC	10529
rs538340560	snp	C/G			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21127944	GTTAAAAGGAATTAA[C/G]TAATTATTATTAATG	10529
rs538344561	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21114717	TACAGCTACTCCACC[A/T]TTCTTTGATTAACGC	10529
rs538347191	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20830657	TATTCATTATGAAAT[C/G]GTTAAAAGACAAAAC	10529
rs538360280	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21121522	CATAGGAAAAGTCCA[A/C]ATCAATGTATGCCTA	10529
rs538379746	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21097952	AGTGTTACTGCTGTA[A/G]TTTGTGACCCTACGT	10529
rs538402828	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21155206	TCCCTCACACACACA[A/C]AAAAATTTTTTAGTA	10529
rs538403665	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21120972	GCACAGGATCTAAAG[G/T]AACTACATTTTCAGG	10529
rs538407843	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21117643	TTCTGTCCTATATAT[C/T]GCCTAGTTATTCTTA	10529
rs538423329	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20947208	GAAAACAAAAGGCAA[C/T]CTGGACTAGAGGTCA	10529
rs538424350	snp	A/G/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20789082	CTCTCCTGGAGCACC[A/G/T]AGGGTCTTGGGCACC	10529
rs538443126	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21104287	CCTTCTGGAATTTCA[A/G]TTGAAATCATGTTAA	10529
rs538443178	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21097252	GATCACAAGGTCAGG[A/G]GTTCGAGACCAGCCT	10529
rs538447968	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20920193	CCTGTCATATATTAC[C/T]GTTGGAAACATAACT	10529
rs538468080	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21017942	AATTCTGCTTCAGTC[C/T]CTCGAGTAGTTGGGA	10529
rs538476730	snp	G/T			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21130656	GGTTCAAAGAATAAA[G/T]CTCAAGATAAATTAT	10529
rs538479529	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20947189	TTTCAAAGAGTCATA[C/T]GTCGAAAACAAAAGG	10529
rs538484173	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:20800458	ATATATTTACAGGGT[G/T]GTGGTTTCATCTACT	10529
rs538503920	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21103590	CTTTGTATCTACTTA[A/C]TGACTAATGATGTTG	10529
rs538519667	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21025577	CAAAATGCAGGAAGC[A/G]ACATAAGCAAATGGC	10529
rs538523869	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20978188	GATTCAAGTTTATCC[A/G]ACCATAAATATTCCA	10529
rs538527523	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20934820	ACAAGGTGCAACCAC[A/G]GCACATAAAATGCAC	10529
rs538534842	snp	C/T	0.00318978	0.0398085	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20861425	CTTCATCTCCTGACC[C/T]ACCTTGGCCTCCCAA	10529
rs538541447	snp	A/C	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20941789	AGCATTCTTATACAC[A/C]AATAACAGACAAACA	10529
rs538541970	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21083556	ATATACCGCTCCTCT[A/C]AGAGAAGTCCTCGGT	10529
rs538549057	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20900777	TTGAACTTGGGAGGC[A/G]TAGGTTGCAGTGAGC	10529
rs538550587	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20936707	CAGTGTTTTCTGTGT[C/T]TCAATTTTCTTTAGG	10529
rs538550788	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20894804	CTTAGTGGCAGGCGC[C/T]TGTGGTCCCGGCTAC	10529
rs538553904	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20784075	TTTGGACTAGTAAAC[A/G]TTTCCTTAAACGATG	10529
rs538567605	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21089502	CCAAAGAGGTGGGGG[A/G]TGACACGGGTGAGTG	10529
rs538574070	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20861902	ATGTAAGTTAAAAAT[A/G]CACCATATACCCCTA	10529
rs538574787	snp	A/G	0.00174672	0.029501	intron-variant, upstream-variant-2KB	NEBL, NEBL-AS1	GRCh38.p7	10:21172482	TTATGCCAATACTGG[A/G]AAAAAAAAAAAAACA	10529
rs538580603	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20786772	TACACTGAATATATG[A/G]ACCAGTTCTTCAAGA	10529
rs538593887	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20915531	TGTTCTTGCGATAGT[C/T]TACTGAGAATGATGA	10529
rs538595004	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20826349	ATAAAGTGAAGAATA[A/G]AAGGAAAAAAGCCAT	10529
rs538596559	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20809578	AAGCATTCTTACTAA[C/T]AAAAAGCTTATTTAA	10529
rs538600564	in-del	-/AAAT	0.00835141	0.0640778	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20856802	GACCAATGATTAAAA[-/AAAT]AAATAAATTTATTTT	10529
rs538608709	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21050181	CCAGGTAGAGTCTCT[C/T]TTTTGCCTGGACATC	10529
rs538618284	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, nc-transcript-variant	NEBL, NEBL-AS1	GRCh38.p7	10:21174873	TGGTCATTTTAGGCC[A/C]GAGTCGAGCCTCTCT	10529
rs538624856	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20965813	AGAACTGTCCCAGGA[C/G]CACAGAAGAAAGCAA	10529
rs538631195	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20802662	TAATGCTCATGAAAA[C/T]CAAATGTGAACGATG	10529
rs538638253	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21114604	ACATTTAGGATTGCT[A/G]TGTTTTCTTGAGAAA	10529
rs538639493	snp	A/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21091972	ATCTTGCATTTGCTA[A/T]TGATATTTTTACCCA	10529
rs538641558	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21002275	ATTGTAGCAGAACTT[C/T]GTGTCCTATGCAGGA	10529
rs538657197	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:20917758	TTTCTGTCTCATGGT[C/G]ACCTTGTCCATAATT	10529
rs538675748	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21056270	TCCTACACAGCCCTC[C/T]CTCTTGTTCATAAAA	10529
rs538678813	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20967485	ATACAAAAATTAGCC[A/G]GGTGTGATGGTACAC	10529
rs538679078	snp	A/G	0.00398564	0.0444627	intron-variant, nc-transcript-variant	NEBL, LOC102725112	GRCh38.p7	10:20879823	AGTCAGGATGAGGAG[A/G]TTTTAAAAAAAAGCT	10529
rs538679444	snp	A/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20886195	AAAAAAAATTTTTTT[A/T]AATAAGATTATCTAG	10529
rs538683099	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21015776	CCTCAGCCTCCCGAA[A/G]TGCTGGGATTACAGG	10529
rs538693099	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20780098	ACTAGCATCCAAATC[A/G]CATAGATTTATATGA	10529
rs538701896	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20797351	TTTTTCTTGAACTAA[A/T]GTATTCTAATACTGA	10529
rs538704908	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20966871	AGGCAGAAAGCCATC[A/G]CGGATGAAGGAAGAA	10529
rs538705221	snp	C/G	0.0023933	0.0345097	upstream-variant-2KB, intron-variant	NEBL, NEBL-AS1	GRCh38.p7	10:21174227	CGAAGTGGCAGGGAA[C/G]GTGCACGTCGGGCAC	10529
rs538706847	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21166604	TGCCAGACACCAGGC[C/T]ACGGCCTATCCTAGT	10529
rs538718997	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20827588	TTAGAACAGAAGTCA[A/G]GTTTATACATTTATT	10529
rs538733251	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21077904	ACTATTCATGACCAC[A/G]AGAAAGTACTTTAGC	10529
rs538760984	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21090754	TTTTGTCATTAGCCA[A/G]TTTCCTCCTGGCTCA	10529
rs538761962	snp	C/T	0.00119737	0.0244387	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21134991	CCAGACATGGGATTA[C/T]TCAGCTCGATTATTC	10529
rs538766849	snp	A/T	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20959790	AAAAGTTTTTTTTTT[A/T]AAAAAAGATGTTGTC	10529
rs538790576	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:21079340	GCAGGGAGCACAAAT[A/C]TTTGGTAGGCTCTCA	10529
rs538792466	snp	A/G	0.00279162	0.0372561	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20874452	TCTCTTCTTTTCTCT[A/G]AGATCAGCTGCTGTA	10529
rs538792839	snp	A/C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20851172	AAGCCATCACAATGG[A/C/T]TGGCTTTTTAAGCAA	10529
rs538803529	snp	A/T	0.00953873	0.0683987	intron-variant	NEBL	GRCh38.p7	10:21061510	TATCATATATTACAT[A/T]ATATATTATATATCA	10529
rs538807050	snp	A/G	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21142067	TCACTCTCTGTAATA[A/G]GACAAAAGACCTCAT	10529
rs538826725	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21026038	TCGGAATAAAATATT[C/G]CTGGTTCTCTCATGA	10529
rs538831122	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20867988	GGTCTTCATTTTCAT[A/G]CTTTTAAAGGCTATT	10529
rs538832110	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20985727	GTATGCAGCTATACT[A/G]AACATACAATATTCA	10529
rs538833285	snp	A/G	0.00557542	0.0525036	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21141153	AGACACCAAAAAGAC[A/G]TGAAACAATAAACTG	10529
rs538833999	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20960620	AAATTATACATAATT[C/G]TATCTGCAAATTTTA	10529
rs538836516	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21048102	AAATTTCTGCTGTGG[C/T]AGCTTCACCAGGAGG	10529
rs538847838	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21148614	CACTGCAACTTCCAC[C/T]TCCTGCGTGGAAGCG	10529
rs538854378	snp	C/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20901257	CTTCTGATCTTTTGA[C/T]AGCTTGATGTTTACA	10529
rs538857440	snp	C/G	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:21067512	AGGGAACAAGTAAGA[C/G]AAACAGTTATGTATG	10529
rs538858784	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21083748	TACTTAGGAGGCTGA[C/G]GCAAGAGGATGACTT	10529
rs538872126	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20985825	ACCAGTGTGCATCTC[C/T]ATATAAAAGGACCAG	10529
rs538885508	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20791983	TACAACAGAGGCTGA[C/G]AGATTGAACAGGAAG	10529
rs538886450	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20881305	TTCAAATGATTGGGT[C/T]TGATTTTATGTAGGC	10529
rs538888216	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21054008	ACTGCACTCCAGCCT[A/G]GGCGACGAAGCAAGA	10529
rs538888604	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20786196	AATAATAAAGCCAAG[C/T]TCCCCCCAACTTCAG	10529
rs538905927	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20896909	TCTATAACATAATAA[C/T]ACCACAGGTGCAATG	10529
rs538918996	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:20987860	TCTGACATCACTAGG[A/T]CTTCCACTGACTCCA	10529
rs538923984	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21154624	CAGCACAAACTCTAC[A/G]CATTATCCAAAATGC	10529
rs538924011	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21021339	ATGCAAATCTGATCA[C/T]GTCACTCCCCTGAGT	10529
rs538928723	snp	C/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20799062	TAGATGTACAGACTA[C/G]ATGGTAAAATATAAT	10529
rs538943067	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20998697	CACAGCAATAATACT[A/G]TCCAATCTGCATATT	10529
rs538945670	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20902803	TCTGTATGTGGCTTA[A/T]ACCCAGAACCAAAGG	10529
rs538946456	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	NEBL	GRCh38.p7	10:20779549	GAACACAGCCAAACC[A/G]TATCAAAGCAGATTA	10529
rs538947157	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20943768	AAGTCGTTCAAAACT[A/G]TTCAGTTACTAGGAT	10529
rs538947304	snp	C/T	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21140526	GGATTAATGGGAATA[C/T]AGTCTGTCCAGCCTG	10529
rs538952574	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20978594	AGAACTGGTCTCTAA[C/T]AAAAATTTAAAAAAA	10529
rs538957955	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21031464	CGCCTATTCCTGCCG[A/C]GATGGGAGGCCCAGG	10529
rs538962823	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20819889	GCCACCACACCCAAC[C/G]CTTATCAAATGTTTT	10529
rs538971963	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21153845	AAATAAAAGTATATA[C/T]GGAAATAAACGTAAG	10529
rs538975424	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20953900	TGTACTGAGCTCTAT[A/T]CTAGGCATAACCGAT	10529
rs538981204	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20937257	CCACTGAGAAAGCTC[A/G]ATTTCATATTTTTAT	10529
rs538982403	snp	C/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21022638	TCCTGCCTTCTTAGA[C/G]TATAAACGAATCTAG	10529
rs538989093	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20984897	GATCAGCGGTGGCAT[C/T]AGATTCTCATAGGAG	10529
rs538990324	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20814450	AGGTAAAAATTAAAA[A/G]AAAAAAAAAATTAGT	10529
rs539003120	snp	A/T			intron-variant, utr-variant-5-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20897540	ACTAATTCTATTCAT[A/T]CATAAAAGAGCATAA	10529
rs539003728	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21108003	TGTATTTCTATGGGA[C/T]CGGTGGTGATATCCC	10529
rs539004462	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20992469	CCTCTTTTGAGTGAC[G/T]ACAGAGGCTCCTGGG	10529
rs539019609	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20858186	AACGCTGCAGACATA[C/T]TGGCTTCTTGGAGCC	10529
rs539020105	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20972865	TTTAATCAAAGCATG[C/T]AAAAGATTATTTCCT	10529
rs539042563	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20932211	AGAATAAGTGCCCTT[C/T]GTATACACCATGGAA	10529
rs539044697	snp	C/T	0.00478085	0.0486577	intron-variant	NEBL	GRCh38.p7	10:20942037	TTTGTAGATTCAATG[C/T]CATCCCCATCAAGCT	10529
rs539052115	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21015572	CTGGAGCACAGTGGT[A/G]TGATTACAGCTAACT	10529
rs539055673	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21153341	TTAATTTTTTTTTAA[A/G]ATGGAGTTTTGCTCT	10529
rs539062044	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20901154	CTCATTCTCTGTGCC[A/G]TTAATATCCTTTTAA	10529
rs539068844	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:21039132	GGATATTAGACCTTT[C/G]TCCAATGGGTTACTT	10529
rs539071040	snp	C/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21042701	GCAAACACTGCAAAT[C/G]AGGCCTTTTTGTTCT	10529
rs539075124	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20850728	TAGAACAACTAACTA[A/G]TGTAGTTCTAGGAGT	10529
rs539075722	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21069804	ACATTATTATTGTAT[C/T]CATCTGATCATTATC	10529
rs539079746	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20934706	TAAGCCCCCTCTCTG[C/T]TACCAAGCTGTGTTG	10529
rs539087121	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21036347	TGGTCCCAGCTACTC[A/G]GGAGGCTTAGGTGGG	10529
rs539101530	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20969315	TTACCTTTTTAAACA[C/T]AATTAAAAAGCATTA	10529
rs539102401	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20866707	GAACCTTCTAAGGAC[A/G]CGTCTTTCTTCTCCA	10529
rs539104285	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21111144	GGATAAGAAGAATCA[A/G]TATCATGAAAATGAC	10529
rs539118771	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21156595	TAACTATGCTGCCTT[C/T]GTGCTTTTTTTTTTT	10529
rs539119632	snp	C/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20866153	CCCTAAAATGCTTCC[C/T]ATAATTGCGCTCTGA	10529
rs539121678	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20839321	GATTGGACATGTCAC[A/G]GCAACAGAAGAATTT	10529
rs539123568	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21009662	ATTTCAGAATACAAT[A/G]CAATTGTCCCAAACG	10529
rs539133566	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:20988250	GCCCTTAGCCATGTC[G/T]GGCAACCCCATGACT	10529
rs539134172	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21075663	ATTTTCCTCAACTCT[C/T]AGCTTCAACAATTGC	10529
rs539137911	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21107969	ATAGAGTTATTTATG[A/G]TATTTTCTGATGGTA	10529
rs539139103	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20886883	AAAAGGAAGCATATC[C/T]TTAGAAAGAAAATTT	10529
rs539146971	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21082163	GGGCTTCAAAAGAGT[C/G]GTGAAAGTCACCAAG	10529
rs539149747	snp	C/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20872180	GTGAAGAGAGGTGAA[C/T]GGCACAAAGGCAGCA	10529
rs539164164	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20982806	TAGTGTTGTTTAGTA[A/G]TGTCTATTAAAAGGG	10529
rs539200154	snp	C/G/T			intron-variant	NEBL	GRCh38.p7	10:20932811	CCAAAAGGACAAAAG[C/G/T]TGAAAACTGTAACCT	10529
rs539200662	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21041502	AGAGTTTTGACCTGA[A/G]AGAGAAATTGCTTTT	10529
rs539202084	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20883848	CATTTCATTTACAGC[C/T]GCTACTAAGTACCAC	10529
rs539232756	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20843228	GGTGTCTGCAAGCCG[A/G]TAAGAGGGCCCTCGC	10529
rs539236524	snp	C/T	0.00318978	0.0398085	intron-variant	NEBL	GRCh38.p7	10:20998240	AAATATTAGCAAGGA[C/T]CCTGAGTAGCCGTGT	10529
rs539247394	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20806155	AAAAGAGGTGATTAA[C/G]TAACAGCAGCAGGTT	10529
rs539249077	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20800856	TTCTTAGAAAAGCTC[C/T]AGGAATGGATTAAAC	10529
rs539260336	snp	A/T	0.0379877	0.132479	intron-variant	NEBL	GRCh38.p7	10:21047537	AAATGAAGCTTTTTT[A/T]AAAAAAAAAAAGATT	10529
rs539260952	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20838682	GGAAGAGGCAATTAA[C/T]GTGGCAAACTTCATT	10529
rs539266370	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21038625	ATTGATGGGCATTTG[G/T]GTTGGTTCCAAGTCT	10529
rs539270459	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20953443	AGAAAAATTTCTGTC[A/G]CTTTACGCTGCCCAA	10529
rs539278134	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20914427	TGAGATTACCCTCTA[C/T]GTTTCCTATAAATCC	10529
rs539280356	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:21109126	TTCAGTATGATATTG[C/G]CTGTGGGTTTGTCAT	10529
rs539284105	snp	A/C	0.000199094	0.00997534	missense, intron-variant, utr-variant-3-prime	C10orf113, NEBL	GRCh38.p7	10:21126068	TTCTGGTCTCCCCAA[A/C]CAGCTTCCTGGGAGG	10529
rs539291008	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20884452	TTCAGAAAATTCATA[G/T]ATCTCTAAATTAAAG	10529
rs539291163	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21051439	TGATATGAATTCACA[A/G]CAGATAGTTATAGTT	10529
rs539297833	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21044628	CCACCACACTGAGAT[G/T]TCCAAACAAATCCAT	10529
rs539302383	snp	C/T	0.000798403	0.0199641	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21133567	TAAGAAGAGAAAACA[C/T]AGGGAATCTTCATAG	10529
rs539311551	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20801548	TCACAATGCTTTCCT[A/G]AGCACAATGGTTTTA	10529
rs539315637	snp	C/T	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:21037774	ATAATGGAATGAACA[C/T]TCAAGATAAATTGGA	10529
rs539327358	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20839245	TACTTTGCCATTGAG[A/G]GAATAAAACAACTTT	10529
rs539342468	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20832740	TTATTAGGAGATCCT[C/G]AAATTTAGGTAAGTG	10529
rs539348379	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21050803	TGGTGTCTCATCCTA[C/T]GTAGAATGCAGAAAA	10529
rs539361886	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20950502	ACACTTTTACATCCA[A/G]CCGAGGCCCTCATGC	10529
rs539365535	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20907993	TGGGAAAGAGGAACT[C/G]CATATAAAAATGATG	10529
rs539393222	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20822819	GATTCAAAGGTACAA[G/T]AACAGTTGTGTTACA	10529
rs539395102	snp	A/G	0.00279162	0.0372561	intron-variant, downstream-variant-500B	NEBL	GRCh38.p7	10:20817155	GAGGCCAAGGTGGCC[A/G]GATTGCATGAGCTCA	10529
rs539405351	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21017857	AAAATAGAGTCTTGC[C/T]CTGTTGCCCAGGCTA	10529
rs539421861	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21029882	ATGACTACAGAGGAG[G/T]CAGGGACCGCTATGA	10529
rs539425250	snp	C/G	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21137082	TTTGTCTACAGGGAA[C/G]TGATTAAAGCATGGT	10529
rs539435884	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20905322	CATACCCGAGACTGG[G/T]TAATTTATAAATAAA	10529
rs539444961	snp	A/G	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21143208	AATCCCAGCACTTTA[A/G]GAGGCCAAGGTGGGC	10529
rs539460511	snp	C/T	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21143773	AAGGTTGCTTCCAGC[C/T]TTTACGAACAAATAA	10529
rs539465244	snp	C/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21011754	CTAGCGGTACCCCCT[C/G]AAGACACTTCCTTCC	10529
rs539467147	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21018580	AACCAACAGTAAATT[C/G]CACTTGGAGATTATT	10529
rs539491811	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21033987	CCTGGGCAAAATAGC[A/G]AAAACTCATCTCTAC	10529
rs539498367	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20935016	ACGATTTTATTTATT[C/T]GTTAAAACACTTACT	10529
rs539513480	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20982194	ATATGGTTTAGGAAT[A/G]CATCGTGTAGTTACA	10529
rs539516032	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20905732	ACCCAGAGACAAGAG[C/T]TGAAAGAACCAAAAG	10529
rs539524320	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20974237	AACTTCAAAGACCAT[C/T]GCTTAGTTTTTTTTC	10529
rs539529096	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21012272	TCTGTTTCTCTCTCT[A/G]GGGCCACAAGTGTGA	10529
rs539534045	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21039417	ATAAGGTGTAAGGAC[A/G]GGTCCAGTTTCTGTT	10529
rs539536542	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20929210	AAAATACGGAATCAA[C/T]CTAAGTGTCCATCAA	10529
rs539540528	snp	C/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20999845	ATGTCTTTCTTCTCC[C/G]ATAATAATCTATACT	10529
rs539541142	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21149975	AAAAGCAGAGGAAAA[A/G]CAGTTTGTGTTTTTT	10529
rs539558037	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20812470	TGCTATCCCTCCCCC[A/C]TCCCCCCACCTCACA	10529
rs539561284	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21124685	AGGCCGAGCATAGTG[G/T]GTCATAGCTGGAATC	10529
rs539574198	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20922525	AAATCTAGTCTATTC[C/T]TTCTCATCAGCAGGA	10529
rs539575238	snp	G/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21026775	AAGGCCTGCTTAGAA[G/T]GATGGCCCTTCTCTG	10529
rs539596805	snp	G/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21045186	AGTGAGTAATCTTTT[G/T]TATGGTTTCTGAATT	10529
rs539598257	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21068204	AATGTGTTGAACACT[C/T]TTATAAAGTTAAAAA	10529
rs539602408	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21123999	TCACTGGCACCAATC[G/T]ATGACATTTTATGCA	10529
rs539607446	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21013085	GGGTACAATGGGGGC[A/G]TGGGGGCAGGGTGGG	10529
rs539607885	in-del	-/C	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20894893	GAGATCGTGCCACTG[-/C]CCTCCAGCCTGGGTG	10529
rs539613775	snp	A/C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21122786	AAATATGACAGATCA[A/C/G]TTTCCTAAGGAAAAG	10529
rs539626279	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21109730	GGTTTAGTCTTGGGA[A/G]AATGTATGTGTCCAG	10529
rs539630750	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21087696	AATGTGTGACAATTA[G/T]TTCCGCTGTTTGAGG	10529
rs539633347	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21032952	CTATGAAATGCTTAT[C/T]GGCTATTGAAACATG	10529
rs539634213	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20812233	ACAATTATTTTGTTT[C/T]TCTTTTTAAAGAAAA	10529
rs539642646	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20848156	TGGGTGGCTCTACTC[C/T]ATCCAAAAAGTGCTG	10529
rs539651501	snp	A/G			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21136295	CCAAATACAACTGGC[A/G]ACTGTTGAAATCCAA	10529
rs539652600	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20930551	GTAAAATCCTAGCTC[C/T]ACCATGGCCCTGCCT	10529
rs539662960	snp	C/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	NEBL	GRCh38.p7	10:20819325	TGGTTTTACGTTCCT[C/G]TGTTAGTTTGCTAAG	10529
rs539664736	snp	G/T	0.000798403	0.0199641	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21130149	GGGAAAGTCATCTGG[G/T]ACAAAGAAAGCCATT	10529
rs539670893	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21013766	ACCTATAATCCCATC[C/T]ACTCGGGAGGCTGAG	10529
rs539684803	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21094311	ATCGAGACCATCCTG[A/G]CTAATACGGTGAAAC	10529
rs539687577	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21115803	TTTTTTCTGTTCCTT[C/T]CCAATCCGCTCTTAA	10529
rs539697552	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21038286	GCCATGGTTGTTTGC[C/T]GCACCTATCAACCCG	10529
rs539704662	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21162008	TGAGCCGGATGAGAT[A/C]AGCTGACCTTTTCCA	10529
rs539748722	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:21100303	TGTTGACTGTGTTTC[G/T]TTCATCCCACTTGCC	10529
rs539765030	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21122292	CAGCCTCCCAAAGTA[C/T]TGGAATTACAGGCAT	10529
rs539765926	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20814757	GTTAAAAAATGCATA[C/T]AAGCTACTCTATTTC	10529
rs539769766	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20917738	GTCTATAAAATTAAT[A/G]TGTGTTTCTGTCTCA	10529
rs539770649	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20807141	ACCAGCATGGACAAC[A/G]TTGCGAGACCCCCGT	10529
rs539775029	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20924628	ATGTGAAAGAATAGG[C/G]CCTCCTGGAATAAAT	10529
rs539778300	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21100143	CCCGGCCATCACATT[A/C]TATTGACTCTTTAGT	10529
rs539807661	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20911575	ATAGTCTTCAAACAA[C/T]TACAAGGACATTCTC	10529
rs539810448	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20819633	CATTAATAAGATCAT[C/T]ATCAGGATTTCATAG	10529
rs539834508	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21099351	TCCCTCCTCTCCTTT[C/T]GCGTCCTCCCCTGTC	10529
rs539844621	snp	A/G	0.00279162	0.0372561	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20866130	GATGTTTACTTTTTG[A/G]AATTGAACCCTAAAA	10529
rs539880835	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21021676	GGGTCAGGAATGGCC[C/T]CTGGATGGACTTTTC	10529
rs539884367	snp	A/C	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21027302	TAACGTATTATCTTT[A/C]AAAAAAAAACAACAA	10529
rs539900885	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20786681	GACCAAGAGACTATG[C/T]TGAGGGCTTGTAGAA	10529
rs539906269	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20866815	CTACTAATAAATTTG[A/G]GCATCTTTTCACCTG	10529
rs539912497	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21068906	GTTGTTGTTGTTTAA[A/G]ACTGATTCTCACTCT	10529
rs539929754	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21067890	AGGCTGAGGCAGGAG[A/G]ATCACTTGAGCGCAG	10529
rs539932217	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20931892	TAAGGAAAGAAATAA[C/T]AAAGAAATCAAACAT	10529
rs539942516	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21015443	GTGTGCTACACAGCC[C/T]GAAAAAGGGAATGCT	10529
rs539946584	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21109484	TTGTGTCTCTGCCAG[A/G]TTTTGGTGTCAGGAT	10529
rs539950157	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20982652	CTGACAAGCATCTTA[C/T]TTATACCTTTTGGGA	10529
rs539951926	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21008441	AATTTTTTTCCACAG[A/G]TTTTTGGGGAACAGA	10529
rs539954410	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21155779	CAAGGGAGGTGCGTT[C/G]GAAAAGCACTATCAC	10529
rs539980501	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20820354	AATAAATGAGCATCA[A/G]TAGAGAAAATCAGAA	10529
rs539986973	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21019924	AACAAAACTGAGAAT[A/G]TCAGGACAATTCAAG	10529
rs539990604	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	NEBL	GRCh38.p7	10:20815380	GTTGTTTAAATGAAT[A/G]TAATTTTAACCTAAG	10529
rs539992674	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20932423	AGGGCCTGGGGCTGG[G/T]GGGTGGGGGAGAAAG	10529
rs539995469	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20940862	AAATTCCTCAACACA[C/T]ACAAACTCCCAAGAC	10529
rs539997880	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21074729	ATGATCCGCCTGCCT[C/T]GGCCTCCCAAAGTGC	10529
rs540009135	snp	C/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20925649	ACTCCTTAACCCACA[C/T]ATTTAGAAAGATGTT	10529
rs540010184	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20859889	CACATATGATTTTCA[C/T]GTAGATAAAATAAAA	10529
rs540036527	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20970819	AAGTCTCTCTGACAT[C/T]CACCTGCCCAGCATC	10529
rs540040107	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21161672	TTCTAATCTTCCCCA[A/G]CTTCTATTGACTGAC	10529
rs540044494	snp	C/G			intron-variant	NEBL	GRCh38.p7	10:21091824	TTTTGTAGAAATGGA[C/G]TCTTGCTATCTTACC	10529
rs540045471	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21162638	CTCACCTCCCACTCC[A/G]GGCTGAGAATATCTA	10529
rs540048804	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20854385	GATGACCAAGTGGCC[C/T]GCCACAAGAGAGCTA	10529
rs540050088	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20892498	TGTGGAGGCTGGGGA[A/G]ACAAAAACCTACTTG	10529
rs540053649	snp	G/T			intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20958491	GAACATTATCTTCAA[G/T]TAAACGATTTGGCTC	10529
rs540054581	snp	G/T			intron-variant, upstream-variant-2KB	NEBL, LOC102725112	GRCh38.p7	10:20844551	GTGGACTATAGACAT[G/T]ATATTTTTAGTTTTA	10529
rs540058212	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20896587	AAAATGTTAAAAAAA[A/T]GACTATTCATTTAGA	10529
rs540058910	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20935701	CTTAAATAATCTTGA[C/T]GCTTATCACAATGCT	10529
rs540059529	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21099292	CTATAACCTCACACA[C/T]TGAGTAGCCCACCCA	10529
rs540061231	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21074434	ATGATTATATTGTAC[A/C]TCTCTTGTAAAATGC	10529
rs540064451	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20850909	TCAAGAACAAGAAAG[A/G]AAACATGGGTATGAT	10529
rs540083094	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21003880	AAATGTATGAAAGGG[A/T]ATAAAAAATATCTGA	10529
rs540090232	in-del	-/TT			intron-variant	NEBL	GRCh38.p7	10:20971447	TAGAATTTTTTTTTC[-/TT]TTTTTTTTTTTATTA	10529
rs540097830	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21121748	CCACAACACATGACA[G/T]TTAACTCCCCTAATT	10529
rs540110925	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21049417	GAACTTAGCAAAATT[A/C]TTTATTCTAACCAAG	10529
rs540120479	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20930963	TAAACATACAAAACA[C/T]AGAAACAAACGCCTG	10529
rs540129016	snp	C/G	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21167576	TGCTACTTCTAAGTG[C/G]TAATACCTCTCAAGA	10529
rs540133592	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NEBL, LOC102725112	GRCh38.p7	10:20844801	TCAAATGTCAAGAAA[A/G]GGAGAGAACTCTGGT	10529
rs540145103	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21003982	ATCCATGAATGTATC[A/T]AATGTGTATCACGGC	10529
rs540158707	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20965327	AGCGAGACAAGGGGA[C/T]GTGAAGTGTCAGGCA	10529
rs540163376	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20849475	GTGATCAGGCCATAG[C/T]GCTCTGCCTCATGAA	10529
rs540168010	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21085340	TTAAAACAGCACGTA[G/T]GCCAAGTATGGTGGC	10529
rs540172351	snp	A/T	0.00159617	0.0282053	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20851163	ATAATATGTAAGCCA[A/T]CACAATGGTTGGCTT	10529
rs540176203	snp	G/T			intron-variant	NEBL	GRCh38.p7	10:20890885	ATTGAGAAGATGCAG[G/T]TAATTTGCTAAAAGT	10529
rs540181389	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20960740	ATATACATGTATACA[C/T]ACATCTCATGATGAT	10529
rs540184564	snp	A/G	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:21003342	CTCACACTTTTTCTC[A/G]TGTCTTGTTTCTGTT	10529
rs540185859	in-del	-/AA	0.00597247	0.0543191	intron-variant, utr-variant-5-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20897300	GACGTCTCTGGTGCT[-/AA]CTGGCAGAAATGCCC	10529
rs540190526	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20920494	ATACCGCTAAGGAGT[C/G]CAGGATACAGCAATA	10529
rs540191445	snp	C/G	0.00398564	0.0444627	intron-variant	NEBL	GRCh38.p7	10:20941564	CTCCTATTCAACATA[C/G]TGTTGGAAGTTCTGG	10529
rs540194755	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20868351	GTGTGTAGGTTAAAA[C/T]ACAATTATTTAGTAT	10529
rs540204401	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21094346	TCTCTACTAAAAATA[C/T]AAAAAATTAGCCGGG	10529
rs540217020	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20947604	AAACAGCACTGATGA[A/G]CTTCATAGTTGTTTA	10529
rs540219667	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21120783	TGAGGAAGAACACAC[A/G]CCCAAGTGAGGTCTG	10529
rs540223046	snp	C/G	1.67198e-05	0.0028913	missense, upstream-variant-2KB	NEBL, NEBL-AS1	GRCh38.p7	10:21173782	TATCCAGGCAGTTGA[C/G]TTTCTCGGTGGGATA	10529
rs540249439	snp	A/C	0.0119091	0.0762411	intron-variant	NEBL	GRCh38.p7	10:20953665	CAATCCTTTGATAAA[A/C]CTATAGAAGTCACTG	10529
rs540257008	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21149534	GACCTCAAGTGATCC[A/G]CCTCTCTTGGCTTCC	10529
rs540257812	in-del	-/AAA	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20985189	GTGCCCCATCCATGG[-/AAA]AACTGTCTTCCACAA	10529
rs540264180	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21092645	GGCTCACCACCAGAG[C/T]AGCACCTGCCAGTTC	10529
rs540267518	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21090961	TACCAAAAATGCCAA[C/T]TTTTTCCCAGCGTCC	10529
rs540272031	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20947992	CTAACAAAAGGTACA[C/T]GTATAAATCTCATAA	10529
rs540278875	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20861529	TTTTACCATATTTTC[A/G]TCACTGGTTCTGTCT	10529
rs540293127	snp	G/T	0.00755907	0.0610114	intron-variant	NEBL	GRCh38.p7	10:21155393	ATTCTAACTATTTTT[G/T]TGGTACCCATTAACA	10529
rs540298494	snp	A/G	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21055407	CAGAGGGTCTGTGGC[A/G]TCAAAGCCACAGATC	10529
rs540304762	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20934667	GCCTGGATCCCTGAA[C/T]GACTGCATGGAACAG	10529
rs540305225	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20972650	TACTCGGGAGGCTGA[A/G]GCAGGAGAATTGCTT	10529
rs540306016	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21074557	ATCTTGGCTCACTGC[A/C]ACCTCTTCCTCCTGG	10529
rs540310012	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20855740	TTCCAAAACTTTAAT[C/T]AGAATGATTTTACAC	10529
rs540314287	snp	A/T	0.00478085	0.0486577	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21134477	AGAATTTTCTGCATA[A/T]GTTTCCTAAATTTTA	10529
rs540320729	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20888691	CTCTAGCCTGCACTG[C/T]CTTTAAGCCATCTCA	10529
rs540322376	snp	A/C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20952000	GCTAAACTGCTAGCA[A/C/T]GGGACATGTGAAGTC	10529
rs540322572	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21061306	ACATATTACATATTA[C/T]GTGATATGTAATATA	10529
rs540325242	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21097526	TTTCTATAGCAATAG[A/G]CTGACCTCCATTTCA	10529
rs540332897	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20948531	AATGTGAAATAGTTA[C/T]GGAAGTGTTTACAAT	10529
rs540334680	snp	A/G	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20942558	TCTAAAACACCAAAA[A/G]CAATGGCAATAAAAG	10529
rs540337968	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20892108	CCACTCCCATTATCT[C/T]CTATTAAAAGAGCCC	10529
rs540360606	snp	A/C	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20833114	AGACTACATTAGACA[A/C]CCTTTGCATCAGTTA	10529
rs540362894	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20814711	CAAAGTTATTTTGTT[C/T]CTAAATTTCCCAATT	10529
rs540371132	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21162165	GCACCAATGTGCCAG[C/G]AAGAAAACACATATT	10529
rs540374035	snp	G/T	0.00517822	0.0506191	intron-variant	NEBL	GRCh38.p7	10:20901307	TTAGCAACTGTCAGG[G/T]GGGTAATTCAAGTCT	10529
rs540375409	snp	C/G	0.00279162	0.0372561	intron-variant	NEBL	GRCh38.p7	10:20808406	AATTCTCAAATACAG[C/G]CAGGATAGATGTTCA	10529
rs540382603	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21060969	TGGCTATTAAGGGTT[C/G]AACTGTGCCCCCGAG	10529
rs540382657	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21067182	TTCACCGTGTTAGCC[A/G]GGATGGTCTCGATCT	10529
rs540386732	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20862795	CTGGAAACAAATGAA[A/G]TTACTCCATATGACT	10529
rs540395551	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20850324	CCAGACCCACTGAAC[A/G]TTCTGCGTCCTTTCA	10529
rs540405352	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21027516	TATTTTTTTGTTGAG[A/G]TGGGGTTTCACCATG	10529
rs540419509	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20968916	ATGTATAGTTCTTGT[A/G]TAGTTCATCATCATC	10529
rs540425987	snp	C/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20868966	CTCAACTTTTTGCAG[C/T]AAAATAATTACTAAC	10529
rs540437581	snp	A/C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20974150	CAGGATTCAAACCCA[A/C/G]ATCTGCTGTCCCCAA	10529
rs540447633	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20787640	ATTCGACCATGTGAT[C/T]CTTTTTGGCATTTTC	10529
rs540463709	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:20901731	TGGTTTTTTCACACT[C/T]ATTTTTTGTTGCCTG	10529
rs540464043	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20887036	GAGAGAGCTAAAGAA[C/T]AGATTAACAAAATAA	10529
rs540464765	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20781602	ACAAAAAATCCTATG[C/G]CATTCCCAGGAATAT	10529
rs540468190	snp	G/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21043662	ATCACCTTTCCTAGT[G/T]AGAGAGTTGCACACG	10529
rs540470991	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20863323	GGCACAAAAAAGCAG[A/C]CCCTGAATGAAGGTG	10529
rs540473754	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20980267	CATACTTTTGTCCAG[C/G]TCTGGTGGTCACAAA	10529
rs540516564	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20920034	AACAGATACAAATGG[A/T]CCTTAGTGTAAGAGA	10529
rs540518180	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21049749	GCAGTGACATCCCCT[C/T]CTTTGCAGGCAAAGG	10529
rs540527425	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20997853	ATTTATTCAATACCA[C/G]TTAAGATGGGTACAG	10529
rs540531504	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21043155	TGTATCTTAAAAAGG[G/T]TCTCAGACGATATCC	10529
rs540536377	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21036530	ACCCCTTAGTTGATA[A/G]TCAATGAATAGGAGC	10529
rs540540734	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21051343	GTACACAATGTGTAG[A/G]GATGTAATTTGTGAT	10529
rs540541149	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20899226	TTATTTGGAAATAGG[A/G]AGGAGTAATTTCTGT	10529
rs540543039	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20953097	ATCATTCCCCATTCA[G/T]CCCTGGTATGGACTG	10529
rs540553057	snp	A/C	0.0221141	0.102801	intron-variant	NEBL	GRCh38.p7	10:21091523	TATCCAATTAGCTAT[A/C]AGTACCTCAAGTTTC	10529
rs540553236	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20914182	GCGTTTGAACTAAGA[A/G]ACATTTAGCTGTGGA	10529
rs540553471	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21072571	GTCGGCTGCCACACA[A/G]GAAAAACAAAGGACA	10529
rs540558154	in-del	-/T			intron-variant	NEBL	GRCh38.p7	10:21003023	TTTTTTTTTTTTTTT[-/T]CAAATTTAGCCCTAA	10529
rs540558942	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20968429	GACAGGAGGAATACC[C/T]CAGCCCAGAAGTTCA	10529
rs540574292	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20875395	GAACTACATCCTCCA[A/G]AGTACCTTTCCTTAA	10529
rs540579673	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20893691	AAGGGGATGATATAG[A/C]AGTGTCTACAGGTCT	10529
rs540588868	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20881564	AAAGAAGAACCTAAA[A/G]ACAGCAACCAAGTTA	10529
rs540591625	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21053224	TCCCCCCTACCATCT[G/T]GAGCATATACAATGT	10529
rs540593474	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20992302	TTCCACATTTTAAGT[C/T]TTGCCTCTCACCAGG	10529
rs540598802	snp	A/G	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21135605	TTCTGCTAAAGAAAA[A/G]AGAAACAGCTCCTAT	10529
rs540616197	snp	A/G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21170520	AACCAGTCATTTATG[A/G/T]CTCTCTGGAAGGGAA	10529
rs540619142	snp	A/C	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20798872	CAAGTGCTATTCATT[A/C]GTATTTGATCCTTTC	10529
rs540623343	snp	A/C			intron-variant	NEBL	GRCh38.p7	10:20822547	TAGGTAGTAGTCTAA[A/C]TAGATATAGAAAGAC	10529
rs540625678	snp	C/T	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21142303	CCCTGTCTACTAGCA[C/T]AGCCTGAGCCACCTA	10529
rs540630053	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:21162590	TTCAAGGAGCAAAGC[A/T]CTTGCAGGCTGACTT	10529
rs540631538	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20799229	GGCGCAATCTTGGCT[C/T]ACTGCAACCTCCACC	10529
rs540638523	snp	C/T	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21132701	TTATGAAGTGTCTCA[C/T]TGTGGTTTTGATTTG	10529
rs540639559	snp	A/G	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21134868	CTCTGCAATGCTGCC[A/G]TGCTTAAAACAGTTT	10529
rs540645495	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20841853	ATGCAATTTAAAGAA[C/T]TGGAAAACCAAAACA	10529
rs540651019	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21149580	ATAGGCATGAGCCAT[C/T]GCGCCCGACCTGTAA	10529
rs540651029	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20907766	CCTTCATCAGTGAGG[A/G]AAAACACAGTATTTC	10529
rs540657745	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20872118	CTTTCAGAAATCTAA[A/G]CTTTACATGGGTTAC	10529
rs540664828	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20878412	TAGTGCAAAGTGACA[C/G]TCTGCATTATGAAAG	10529
rs540681443	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20795387	TGTGTATGTGGTTGA[C/T]GAGGTATGCTAAAAC	10529
rs540733724	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20790201	TTTATTGATTATTCT[C/T]ATTTGCCATCTGGCT	10529
rs540737501	snp	G/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20858620	TTTCACAGTAACTCT[G/T]CTTTCAAAAAATAAA	10529
rs540761600	snp	C/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20979803	CCTCTAACTCTTGTG[C/G]TCAAGCAATCCTCCT	10529
rs540762313	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20829116	CATCTTACAGATGGA[G/T]AAACTGAAGTACTAG	10529
rs540764347	snp	A/G			intron-variant	C10orf113, NEBL	GRCh38.p7	10:21136680	CTACCCTACGGCTGG[A/G]CAAAGCTCGCCAAAG	10529
rs540764478	snp	G/T	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21145778	GCAACAAGGCTAACC[G/T]GCACGCAAACCCTGT	10529
rs540765885	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20995267	ATGCAGGGCAGACAT[C/T]ATAAAAAAATGATGT	10529
rs540775220	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20903491	AAGTAGAGCTACCAT[A/G]GGATTCAGCAATCCC	10529
rs540776211	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20944792	TAATTGGCATTGCTT[C/T]GACATACAGAGATAC	10529
rs540776772	in-del	-/GTTGTTGTTGTTGTT	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21122003	TGGGGATTTCTCCTG[-/GTTGTTGTTGTTGTT]GTTGTTGTTGTTGTT	10529
rs540779563	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20908582	ATTTATGAGCAGTAG[C/T]GAGCTGGCAAATGTT	10529
rs540782901	snp	C/T	0.00159617	0.0282053	intron-variant	NEBL	GRCh38.p7	10:21057902	ATATTTAAAGCCAGA[C/T]TTATTTTTGCATTTC	10529
rs540788436	snp	A/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20827698	CAATGATAGACTGGA[A/T]AAAGAAAATGTGGTA	10529
rs540804452	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NEBL	GRCh38.p7	10:20898874	ATGACCGACTGCTTA[A/G]GGAAACATTGCTCTA	10529
rs540812340	snp	C/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:21108890	CTCTTCTTGGTGAAT[C/T]GATCCCTTTACCAAC	10529
rs540821676	snp	C/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21062283	CAGAAGTTAAGGGGA[C/G]GGGAAAGAAGAAAAA	10529
rs540829238	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:21114147	ATTTACTTCAAAATA[C/T]TTTCTAATTTCACTT	10529
rs540835498	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20939813	AAGCAGACTTTAAAT[G/T]AACAAAGATCAAAAG	10529
rs540838400	snp	C/T	0.00557542	0.0525036	intron-variant	NEBL	GRCh38.p7	10:20976921	ATTCCTGAATCTACA[C/T]TAAAAAAAAAAAAAA	10529
rs540842992	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:20893555	TATACTGATGCCCAA[A/T]GTGAAGCCACTTGAC	10529
rs540851935	snp	A/G	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:20900973	CAGTGAGCCAAGATC[A/G]CGCCACTGCACTCCA	10529
rs540855796	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21100534	TTCCCGTGAACCCTG[A/G]GGGGCTGACCTCTGT	10529
rs540860691	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20832084	TCAAATCTCTGGACT[C/T]AGCTGGGCTTAAATA	10529
rs540866998	snp	C/T	0.00119737	0.0244387	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20784331	AGACTCTGGATGAAA[C/T]TTCAAGACCCACCAG	10529
rs540867220	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21016780	GGAAATGCTCTCATG[A/C]AGAATCAAATCATTT	10529
rs540874037	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20782220	AATAAAATATTACTA[A/T]AGAATAGGCAGCAAC	10529
rs540875537	snp	A/C	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21108181	TTCTGCTCTGATCTT[A/C]GTTATTTCTTGCCTT	10529
rs540879743	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20795535	CATCTGACAAGTCTC[C/T]GGGGAGAGAGAGTGT	10529
rs540884761	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21070589	ATAACCTAAGTGGGC[A/G]ATTAGATTTAATACC	10529
rs540893056	snp	C/G	0.00199481	0.0315187	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21144819	AAGTGACTGTAACTA[C/G]CTATTCACGTCATAT	10529
rs540909117	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20791300	ATTTTCTGCTTAATG[A/G]TTATTATTAAAATGG	10529
rs540917644	snp	C/T	0	0	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20859554	ATTAAAAATTAATTA[C/T]AATAATATATTTTTC	10529
rs540921037	snp	C/T			intron-variant	NEBL	GRCh38.p7	10:20936113	CATGCCAAAATCTTT[C/T]CTCCATTTTCAGTTT	10529
rs540927948	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21157510	TGGGAAGCAGAGGCT[A/G]CAGTGAGCCGAGATG	10529
rs540930772	snp	C/T	0.0267878	0.112589	intron-variant	NEBL	GRCh38.p7	10:21010421	AGCGAATTTTTTAAT[C/T]TTTTTTTTTTTTTGC	10529
rs540937955	snp	C/T	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20895475	ACCTCTCTGTGCCTC[C/T]ATCTCCTCGCTTCAG	10529
rs540963138	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20970977	GAATATTTCTTAGTA[C/T]AGGATGCCAAAAGAT	10529
rs540979808	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20994239	TGTCATACTTAATTG[C/T]TCTCTTTAGTCTCTC	10529
rs540984532	snp	A/G	0.00676609	0.0577691	intron-variant	NEBL	GRCh38.p7	10:21046220	ATGGTGATTACCAGA[A/G]GCTGGGAGATGAGAG	10529
rs540996620	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:20966641	ACAGCCTGGACACCG[A/G]AGCAGTTCTGGACCA	10529
rs540998549	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20956290	ATTAAACAGGGTATG[C/T]CAAAGTGTTTCAAAA	10529
rs541001521	snp	C/G			utr-variant-3-prime, nc-transcript-variant	NEBL	GRCh38.p7	10:20780054	GGATTATGAGCCAAA[C/G]AGAAAGTTTTACAAA	10529
rs541014221	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20971855	CCTGACCTCGTGATC[C/T]GCCTGCCTCGGCCTC	10529
rs541018733	snp	A/T			intron-variant	NEBL	GRCh38.p7	10:20804864	GAGTGACATGATGTC[A/T]CCAGGGTTTCAAGAA	10529
rs541019023	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21088668	AAAAGACAGAGTGCA[A/G]GCATCAGATGCACAC	10529
rs541026864	snp	A/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20800993	GTTCCCTTGAGCCCT[A/G]TCTCTGCAGAGATTG	10529
rs541034878	snp	G/T	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21131771	AAAGTTTGGGAAAAG[G/T]AATAAGGAGAAGAAA	10529
rs541037152	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20801671	ATACTAGATAAATGT[C/T]TGATGACTGAGCAGA	10529
rs541043142	snp	C/G	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:20994885	GGAGGAGGAGGTAGA[C/G]GGGGGGGTTGGTCTT	10529
rs541043727	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20917475	CTGAAAGTTGAGACT[G/T]TTCAGGGGATGTCTA	10529
rs541050454	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21019875	ACATTGACTCTGACC[A/G]GAACTCATTTACTTG	10529
rs541051727	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21052828	TACAGACAGAAAATG[C/T]TCAGCCCCAACCTGT	10529
rs541055781	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20878803	TAAGTACACAGTATT[A/G]AATGAAGGAGAAAAG	10529
rs541058011	snp	C/T	0.00557542	0.0525036	intron-variant	NEBL	GRCh38.p7	10:20943139	AAAGACACATGCACA[C/T]GTATGTTTATTGCGG	10529
rs541066960	snp	C/T	0.00119737	0.0244387	intron-variant	NEBL	GRCh38.p7	10:21039156	GTTACTTGCATAAAT[C/T]TTCTCCCATTCTGTA	10529
rs541070735	snp	C/T			intron-variant	NEBL, LOC102725112	GRCh38.p7	10:20862352	TCCCTCATTAATGAA[C/T]CACAATAGTAACATA	10529
rs541071314	snp	A/G	0.0023933	0.0345097	intron-variant	NEBL	GRCh38.p7	10:21124346	ATTAATGCAGGAACG[A/G]AAAGAAATCCAATAC	10529
rs541076997	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20924151	CCAGGAGACATTCAG[C/T]AATATCTAAAGACTT	10529
rs541078774	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21102135	CATCTGCTCTAAATG[G/T]CCAGACTTCTACCAC	10529
rs541092987	snp	A/G	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20796220	ATACAAAAATTAGCA[A/G]GGCGTAGTGGTGGGC	10529
rs541097336	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21116722	TCACTCAGGCTGGAG[G/T]GAAGTGGCACAATCA	10529
rs541097509	snp	C/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:21001379	GAGGTGGAACACAGC[C/T]AGAGTTCTTCCTATC	10529
rs541098223	in-del	-/T	0.00199481	0.0315187	intron-variant	NEBL	GRCh38.p7	10:20901184	AAGTCAAGAAGGGCC[-/T]TCTGCAACTAGACAG	10529
rs541108131	snp	A/C	0.000798403	0.0199641	intron-variant	NEBL	GRCh38.p7	10:21123454	CAACTTTATTCATAC[A/C]CTGAAGATATCAGTA	10529
rs541109912	snp	A/G			intron-variant	NEBL	GRCh38.p7	10:21167111	TGGGTGACTCGTCAC[A/G]AGATGCACCCAGCCC	10529
rs541113229	snp	G/T	0.000399281	0.0141238	intron-variant	NEBL	GRCh38.p7	10:20835895	ACAATTTTCTTTGGG[G/T]CTGGAGGATAGGGAG	10529
rs541115455	snp	C/G	0.000399281	0.0141238	intron-variant	C10orf113, NEBL	GRCh38.p7	10:21138724	TTGGTAACTTGCCCA[C/G]AGTCACACAGCTAAA	10529
rs541119635	snp	A/G	0.00119737	0.0244387	intron-variant, utr-variant-5-prime	NEBL	GRCh38.p7	10:20957944	CAGCTAATTGAAAGT[A/G]CAGCTGATATTAGTG	10529

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