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

ANKRD13B

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs13723	snp	C/T	0.494774	0.0508504	utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant	CORO6, ANKRD13B	GRCh38.p7	17:29614868	CTCCTGGGCTCAGGG[C/T]CCATCAGGCAGCCTC	124930
rs191315	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29609947	catggcctctcaaag[C/T]gctgggattacaggc	124930
rs330159	snp	A/G	0.4928	0.0595664	intron-variant	ANKRD13B	GRCh38.p7	17:29609976	aaactcctgacctca[A/G]gtgatccgctcacct	124930
rs330160	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29609931	gctgggattacaggc[A/G]tgagccaccatgccc	124930
rs1064133	snp	A/G	0	0	downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	CORO6, ANKRD13B	GRCh38.p7	17:29614729	TTTATTTGTGCCTCA[A/G]AATCAGTCTGGTGCC	124930
rs1443346	snp	C/T	0.161267	0.233723	upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29592507	CCTCCACCCAGCTGG[C/T]CCTTCAGGAAGGGAA	124930
rs1529421	snp	C/G	0	0	intron-variant	ANKRD13B	GRCh38.p7	17:29608580	ACTCTTTCatccatt[C/G]tttcaacaaatattt	124930
rs1971157	snp	C/G	0.442926	0.158996	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29598325	GCATGACCATGAACT[C/G]CATTGTCAAAAATGA	124930
rs2016002	snp	A/C	0	0	intron-variant	ANKRD13B	GRCh38.p7	17:29606882	ggtgaaaacccatct[A/C]tactaaaaatacaaa	124930
rs2114877	snp	C/G	0.29046	0.246704	intron-variant	ANKRD13B	GRCh38.p7	17:29603900	tttttttttgagatg[C/G]agtctctctctctgt	124930
rs2321204	snp	C/T	0	0	intron-variant	ANKRD13B	GRCh38.p7	17:29602675	ttaagttaaggatct[C/T]aagatgaaataatcc	124930
rs3098944	snp	C/T	0.474723	0.109542	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29598794	ggaggccaaagtagg[C/T]ggatcacttgagctc	124930
rs3098945	snp	A/G	0.368733	0.220005	intron-variant	ANKRD13B	GRCh38.p7	17:29597161	GTATGGACTAAACAC[A/G]GTGCTTGCGAGGAAG	124930
rs3098946	snp	G/T	0.123452	0.215605	intron-variant	ANKRD13B	GRCh38.p7	17:29594884	CAGCCTGCTCAGTCC[G/T]ATGGCCTGCCCTCCA	124930
rs3110492	snp	A/G	0.449599	0.150533	intron-variant	ANKRD13B	GRCh38.p7	17:29595257	GCAAGTGTGAACAGG[A/G]AATTCCAGGGTGATG	124930
rs7220401	snp	C/T	0.499908	0.00678851	intron-variant	ANKRD13B	GRCh38.p7	17:29608670	GTCCCGACCTCAGGT[C/T]GCTCTTCTGTGTGAG	124930
rs7226173	snp	G/T	0	0	intron-variant	ANKRD13B	GRCh38.p7	17:29595452	CCTGAGGGTGGGTGG[G/T]CCTTTTACTGCAGAG	124930
rs7406075	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29607562	CTGTCTTTCCGTTGC[C/T]CATAGTGTCTGTCTT	124930
rs8065982	snp	A/G	0.0360663	0.129354	utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant	CORO6, ANKRD13B	GRCh38.p7	17:29614801	GGGGGGAACGCCTAC[A/G]GTGTGGGTTGGGGTC	124930
rs9674809	snp	A/G	0.0535932	0.154675	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29599200	cctggagaacgttcc[A/G]gggaaggCCATTGGC	124930
rs9709449	snp	C/G/T	0	0	intron-variant	ANKRD13B	GRCh38.p7	17:29606612	TAACAAACATGCTTT[C/G/T]TAAgccaggtgcagg	124930
rs9894979	snp	C/G/T	0.0134861	0.0810011	utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant	CORO6, ANKRD13B	GRCh38.p7	17:29614787	ACCTAACTTTACTTG[C/G/T]GGGGAACGCCTACGG	124930
rs9901272	snp	C/T	0.0905309	0.192535	intron-variant	ANKRD13B	GRCh38.p7	17:29605435	acacacacacacaca[C/T]acacacacacatata	124930
rs9911167	snp	C/T	0.46865	0.121211	intron-variant	ANKRD13B	GRCh38.p7	17:29608528	TCTTTTTCACTGTTG[C/T]ATTCCCAGTGGCTGG	124930
rs11080107	snp	C/T	0.495818	0.0455352	intron-variant	ANKRD13B	GRCh38.p7	17:29611406	GGCCCTGGCCCCTGG[C/T]CCTTGAAGCACTCAG	124930
rs11436597	in-del	-/C	0.0955749	0.196603	upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29592886	CGACCTAGGCCCGTG[-/C]CCCCCCCACTTCCCC	124930
rs11447635	in-del	-/A	0.503626	0.064491	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29599386	TAGAGCCTGGCAACC[-/A]GGGGAGCAGCAAAGA	124930
rs11553124	snp	C/T	0	0	downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	CORO6, ANKRD13B	GRCh38.p7	17:29614728	GGGCACCAGACTGAT[C/T]CTGAGGCACAAATAA	124930
rs11651605	snp	G/T	0	0	intron-variant	ANKRD13B	GRCh38.p7	17:29605040	CTCCTTTTTGTGtgg[G/T]cttactgagtttcac	124930
rs12452244	snp	C/T	0.00358779	0.0422022	upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29593043	CTCTTCGGCCACCTG[C/T]CACCCCCAGTTTCAC	124930
rs12601861	snp	A/G	0.444444	0.157135	intron-variant	ANKRD13B	GRCh38.p7	17:29604393	tttgtattttttgta[A/G]acatggggttttggt	124930
rs12943142	snp	C/G			intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29598422	CACCTCCCCAGCACT[C/G]TGGACTCCTTTTGTC	124930
rs12943198	snp	A/C			intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29598475	AATATATTGTTTATA[A/C]TGccctctcccctcc	124930
rs12951819	snp	A/T			intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29598441	ACTCCTTTTGTCATT[A/T]ACCTCCCTAATTATA	124930
rs28699506	snp	A/G	0.0172401	0.0912295	intron-variant	ANKRD13B	GRCh38.p7	17:29600268	TTGGGTCATATTTAA[A/G]AATGGGGCTGGGGAG	124930
rs34249921	in-del	-/G			intron-variant	ANKRD13B	GRCh38.p7	17:29597309	CACACACGTTACACA[-/G]GGAGTGGACTCCTGC	124930
rs34261270	in-del	-/A			intron-variant	ANKRD13B	GRCh38.p7	17:29607063	CCCCAAAAAAAACAC[-/A]AAAAAAAAACCCCAA	124930
rs34361929	snp	C/G			missense, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29612246	TTCATCACCCTGCGT[C/G]TGCCTCCTGGCTTCC	124930
rs34391066	in-del	-/G			intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612843	GGCGCGCGGGGCCAC[-/G]GGGACTCCGCGCCGC	124930
rs34435725	in-del	-/C			intron-variant	ANKRD13B	GRCh38.p7	17:29603398	CTGCTTGCCACCATG[-/C]CCCAGCTAATGTAAA	124930
rs35184780	snp	C/G	0.427879	0.175668	intron-variant	ANKRD13B	GRCh38.p7	17:29601604	ATCTGGGATCATTTT[C/G]TTTCCACCTGAAGAA	124930
rs35204464	in-del	-/G			intron-variant	ANKRD13B	GRCh38.p7	17:29607910	CCCAGCCCCACAGCC[-/G]GGGGCCTCCCCAGCA	124930
rs35244918	snp	A/G	0.00230126	0.0338428	synonymous-codon, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29610753	TTCAGAACAGCACAA[A/G]GGCAAGGTCAAAGGT	124930
rs35416264	in-del	-/T			intron-variant	ANKRD13B	GRCh38.p7	17:29602186	GATCACGAGGTCAGG[-/T]AGATCGAGACCATGC	124930
rs35418248	in-del	-/AC			intron-variant	ANKRD13B	GRCh38.p7	17:29605416	TATATACACACACAA[-/AC]ACACACACACACACA	124930
rs35481781	snp	C/T	0.00523276	0.0508822	synonymous-codon, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29609234	GCTTACCGCGCCCGT[C/T]GTCACCACTCAGCTT	124930
rs35600194	in-del	-/T			intron-variant	ANKRD13B	GRCh38.p7	17:29599865	TTAGCATCTAATTTG[-/T]TTTTTTTTTTTTTTT	124930
rs35831588	in-del	-/T	0.5	0	intron-variant	ANKRD13B	GRCh38.p7	17:29600923	AAATATTTTACTGAC[-/T]TTTTTTTTTTTTTTT	124930
rs35876636	in-del	-/A			intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29599387	AGAGCCTGGCAACCG[-/A]GGGAGCAGCAAAGAG	124930
rs36001900	in-del	-/G			downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	CORO6, ANKRD13B	GRCh38.p7	17:29614659	GACACAAAGAGGGAT[-/G]GGAAGAAAAGAACAA	124930
rs56350121	snp	A/G			upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29593034	GTGCAGACCCTCTTC[A/G]GCCACCTGCCACCCC	124930
rs56988993	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29606722	ATAGTGAGACCCTGT[C/T]TCAAGTAAAAAAAAA	124930
rs57453204	snp	A/C	0.00795532	0.062565	intron-variant	ANKRD13B	GRCh38.p7	17:29597099	CTCGTGGGCTGGGGA[A/C]GGGGCTGAGCAGGCA	124930
rs57541684	snp	A/T	0.5	0	intron-variant	ANKRD13B	GRCh38.p7	17:29606759	AAAAAAAAAAAAAAA[A/T]ATCTTTTGTCTGGGC	124930
rs58154361	snp	A/C	0.0248432	0.108648	intron-variant	ANKRD13B	GRCh38.p7	17:29611208	CTACCTCACAGGGGA[A/C]CAACATGAAATCATG	124930
rs58200244	snp	A/G	0.000798403	0.0199641	intron-variant	ANKRD13B	GRCh38.p7	17:29600090	ACCGTGTTAGCCAGG[A/G]TGGTCTCGATCTCCT	124930
rs58659678	snp	C/T			intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29597632	AGCTAGAGGCCTCTG[C/T]TGAGGAGAAGCTGGA	124930
rs59887630	in-del	-/CTTGCCAC			intron-variant	ANKRD13B	GRCh38.p7	17:29611107	AGAAAGTCAGGGGAC[-/CTTGCCAC]AGATTCTGTATGCCC	124930
rs60464414	in-del	-/TTTTTTTTTT			intron-variant	ANKRD13B	GRCh38.p7	17:29599885	TTTTTTTTTTTTTTT[-/TTTTTTTTTT]GATACGGAGTCTCGC	124930
rs61476683	in-del	-/A			intron-variant	ANKRD13B	GRCh38.p7	17:29602395	TGAGATTCCATCTCA[-/A]AAAAAAAAAAAAAAA	124930
rs62068576	snp	C/G	0.474544	0.10991	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29597550	GGGATAAGGAATCTC[C/G]GTTCTCTTGGTGGGG	124930
rs62068577	snp	G/T	0.475081	0.108804	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29597860	GAGGAGCACCCTGCT[G/T]GCAAGGAAGTGCCAG	124930
rs62068578	snp	A/G	0	0	intron-variant, utr-variant-5-prime	ANKRD13B	GRCh38.p7	17:29599444	GGGGGGGCAACAGCT[A/G]CAAGGTAGTGGAAAC	124930
rs62068579	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29606017	TCCCGGGTTCAAGCG[A/G]TTCTCTTGCCTCAGC	124930
rs62068580	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29606023	GTTCAAGCGGTTCTC[C/T]TGCCTCAGCCTCCTG	124930
rs71138837	in-del	-/A	0.496105	0.0439572	intron-variant	ANKRD13B	GRCh38.p7	17:29603878	AAAAAAAAAAAAAAA[-/A]GAAAGAAAATATAAC	124930
rs71371123	snp	A/G	0.0107246	0.0724382	intron-variant	ANKRD13B	GRCh38.p7	17:29599496	TTGGAGGCAGAGCCT[A/G]CAAGTTTTTCTGATG	124930
rs71371124	snp	A/G	0.5	0	intron-variant	ANKRD13B	GRCh38.p7	17:29600182	CACCCAGCCGTCTTA[A/G]CATCTAATTTGTATG	124930
rs71376569	snp	A/G	0.5	0	intron-variant	ANKRD13B	GRCh38.p7	17:29600062	TTTGTATTTTTAGTA[A/G]AGACGGGGTTTCACC	124930
rs73278696	snp	G/T	0.0103295	0.0711199	intron-variant, utr-variant-5-prime	ANKRD13B	GRCh38.p7	17:29594429	CTGCGCACCAGGTGG[G/T]CTCCCTGGTTTCTGC	124930
rs73280605	snp	A/G	0.0150606	0.0854603	intron-variant	ANKRD13B	GRCh38.p7	17:29600590	CCTGTGGTGAGGAAG[A/G]GGGGCATCTCCCAGC	124930
rs73280611	snp	C/G	0.0573587	0.15934	utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant	CORO6, ANKRD13B	GRCh38.p7	17:29615224	CTCTGCAGCAAACGG[C/G]TTGTGTATGTGTCTG	124930
rs74267071	in-del	-/AA			intron-variant	ANKRD13B	GRCh38.p7	17:29601776	AGAGAAAAAAAAAAA[-/AA]GAATTCTAGGTTGAA	124930
rs74481278	snp	A/G	0.0244538	0.107838	intron-variant	ANKRD13B	GRCh38.p7	17:29609722	AGTCCTTTCCTTGGC[A/G]TCCCATTTACTCTTC	124930
rs74534021	snp	C/T	0.021333	0.101051	intron-variant	ANKRD13B	GRCh38.p7	17:29601644	ACATTTCCTGCACAT[C/T]TGGCAATAAATTCCC	124930
rs74772596	snp	A/C/G	0.0170614	0.0910698	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29598190	AGGGGCCACAGCTCA[A/C/G]AGGCCAACAGGGGCC	124930
rs75662431	snp	A/G	0.0130921	0.0798413	intron-variant	ANKRD13B	GRCh38.p7	17:29595666	GAAACAAGGTCCCAG[A/G]TTCACCCCTACCCCT	124930
rs75784428	snp	A/G	0.0295035	0.117819	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29599387	TAGAGCCTGGCAACC[A/G]GGGAGCAGCAAAGAG	124930
rs75933092	snp	A/G			upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29592923	AGGCAAAATGCCAGC[A/G]GGGGAGGTGCGTCCC	124930
rs76015836	snp	A/C	0.5	0	intron-variant	ANKRD13B	GRCh38.p7	17:29602396	TGAGATTCCATCTCA[A/C]AAAAAAAAAAAAAAA	124930
rs76427692	snp	A/C	0.5	0	intron-variant	ANKRD13B	GRCh38.p7	17:29602395	GTGAGATTCCATCTC[A/C]AAAAAAAAAAAAAAA	124930
rs76738011	snp	C/T	0.000798403	0.0199641	intron-variant	ANKRD13B	GRCh38.p7	17:29600883	TCATCTGCTGACATC[C/T]CTTCTCTTTATTCTT	124930
rs76837021	snp	C/T	0.00953873	0.0683987	upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29591778	TCAACCGCGCCAGCC[C/T]CCTCCCCTGCACTGG	124930
rs77231603	snp	A/C	0.5	0	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29613015	AGGATCCTGTCTCCC[A/C]TAAGCCAGGACACAG	124930
rs77506374	snp	C/T	0.0103295	0.0711199	intron-variant	ANKRD13B	GRCh38.p7	17:29595040	TGGGTGGCCACTTCC[C/T]GTTACCTGTGCCTAT	124930
rs77960128	snp	A/G	0.0298908	0.118541	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29597945	TGGAGCCCTGAGGCC[A/G]GGCAGCGGCCTGCCA	124930
rs78169718	snp	C/T	0.0569829	0.158885	intron-variant	ANKRD13B	GRCh38.p7	17:29605058	TACTGAGTTTCACTA[C/T]ACACATGTGAAGTTT	124930
rs78361036	snp	C/T	0.00318978	0.0398085	intron-variant	ANKRD13B	GRCh38.p7	17:29602579	TCTAGTCTCTGCCTC[C/T]GTCTTCACATGGCCT	124930
rs78918512	snp	C/T	0.00119737	0.0244387	intron-variant	ANKRD13B	GRCh38.p7	17:29606430	TGGCATAGTGGTGCT[C/T]GCCTGTAATCCCAGC	124930
rs78990004	snp	A/G	0.0146672	0.084371	intron-variant	ANKRD13B	GRCh38.p7	17:29611164	CTCTGGGTACCAGAT[A/G]CCGTGTCCGAGGTGA	124930
rs79415967	snp	C/T	0.0267878	0.112589	intron-variant	ANKRD13B	GRCh38.p7	17:29608561	CACTCAGTAGGTGTT[C/T]CATAAATATTTGTTG	124930
rs79449326	snp	A/G	0.0111196	0.0737302	intron-variant	ANKRD13B	GRCh38.p7	17:29596335	AAGGGGCACCCAGCA[A/G]TGCTGTGATGCCAGC	124930
rs79823758	snp	C/T	0.0174175	0.0916809	upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29592750	TTGGTACTGATGCCC[C/T]ACACCTTTCTCAGGA	124930
rs79872689	snp	A/G	0.134802	0.221877	intron-variant	ANKRD13B	GRCh38.p7	17:29594769	CTGGGGGTGGTTAGC[A/G]CAGTTGCCCGCTGTG	124930
rs79996304	snp	C/T	0.0998734	0.199905	downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	CORO6, ANKRD13B	GRCh38.p7	17:29614493	GACTCTAAAACCCTT[C/T]ATCCAATGGTGCTAA	124930
rs80035288	snp	A/G	0.0433465	0.140692	intron-variant	ANKRD13B	GRCh38.p7	17:29610988	GTTCAGTGGAGAGCC[A/G]TGCTGCAAGTGATTA	124930
rs80181893	snp	C/T	0.0074412	0.0605411	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29607837	TGTGCTCCTGGCGCA[C/T]GGCGCAGACGTGGGC	124930
rs80290325	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29592766	ACACCTTTCTCAGGA[A/G]TTCCCAATCAGACGC	124930
rs111430893	snp	G/T	0.5	0	intron-variant	ANKRD13B	GRCh38.p7	17:29601056	CAGCCTCCCAGTAGC[G/T]GGGACGATAGGCATG	124930
rs111487344	snp	G/T	0.5	0	utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant	CORO6, ANKRD13B	GRCh38.p7	17:29614765	CTTCATACCGGAGGC[G/T]TTTGCTACCTAACTT	124930
rs111684891	snp	C/T	0.00939981	0.0679084	intron-variant	ANKRD13B	GRCh38.p7	17:29610656	TAAGACCAGAACTGC[C/T]TATGAGCCCTTTCTT	124930
rs111762441	in-del	-/T	0.5	0	intron-variant	ANKRD13B	GRCh38.p7	17:29604216	TGACCTTTTTGAGGC[-/T]TTTTTTTTTTGAGAC	124930
rs112142287	snp	G/T	0	0	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29599211	TTCCGGGGAAGGCCA[G/T]TGGCGAAGGGTGGAG	124930
rs112151193	snp	A/T	0.5	0	intron-variant	ANKRD13B	GRCh38.p7	17:29609809	CTTAGAGTGGTTCTG[A/T]GACCTGTACAAGGTC	124930
rs112227194	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29596352	GCTGTGATGCCAGCC[C/T]GGTGCCCTGCTTGCC	124930
rs112434381	snp	A/C/T	0.00358779	0.0422022	upstream-variant-2KB, intron-variant	GIT1, ANKRD13B	GRCh38.p7	17:29591582	AAACTTTGTTTCCCC[A/C/T]AGCCCCGTCACAGCC	124930
rs112674011	snp	A/G	0.0130921	0.0798413	intron-variant	ANKRD13B	GRCh38.p7	17:29599940	AGAGTGCAGTGGCGC[A/G]ATCTCGGCTCACTGC	124930
rs112792495	snp	C/T	0.0162398	0.0886349	intron-variant	ANKRD13B	GRCh38.p7	17:29611493	GAACCGGCCTCCTCC[C/T]TAGGTCTTGGGTGCT	124930
rs112896844	snp	A/G	0	0	intron-variant	ANKRD13B	GRCh38.p7	17:29606078	CCACCACGCCTGGCT[A/G]ATTTTGTATTTTTAG	124930
rs113166355	snp	C/T	0.5	0	upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29591677	CCCAGGAAGCAGGAC[C/T]GCTACAGTGGAATCA	124930
rs113310349	snp	A/T	0.5	0	intron-variant	ANKRD13B	GRCh38.p7	17:29595379	AGAACTTCCCAGGGG[A/T]CCAAGGATCACTAGG	124930
rs113343445	snp	C/T	0.5	0	intron-variant	ANKRD13B	GRCh38.p7	17:29601080	AGGCATGCACCACCA[C/T]GCCTGGCTAATTTTA	124930
rs113592129	snp	C/T	0.5	0	synonymous-codon, downstream-variant-500B, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29612451	CACCTTCGGGAACCT[C/T]AACGGCTGCGACGAA	124930
rs113644003	snp	C/T	0.5	0	intron-variant	ANKRD13B	GRCh38.p7	17:29596107	TCAGGAGCCAGGTTT[C/T]CCTGGTCTTGGCTTG	124930
rs114148991	snp	A/G	0.00835141	0.0640778	intron-variant	ANKRD13B	GRCh38.p7	17:29597398	CCTATGAGCGTACGA[A/G]TGTGTATCTGTATGG	124930
rs114300952	snp	C/T	0.0763149	0.179815	intron-variant	ANKRD13B	GRCh38.p7	17:29610148	AGTGTGCAGCGATCC[C/T]GCCACAGCACTCCAG	124930
rs114339079	snp	C/T	0.0429648	0.14013	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29599062	CACTTGGACGGGCAG[C/T]GGATAGAGCCATAGC	124930
rs114355910	snp	A/G	0.0550013	0.156817	intron-variant	ANKRD13B	GRCh38.p7	17:29609467	GCTGCACTCTTGCCT[A/G]CAGCAAGCTGTACAG	124930
rs114797199	snp	A/G	0.00993419	0.0697739	utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant	CORO6, ANKRD13B	GRCh38.p7	17:29615121	TTCGCGGGGGCTGCC[A/G]CGAGGAAGCAGCCCT	124930
rs114946151	snp	C/T	0.00597247	0.0543191	intron-variant	ANKRD13B	GRCh38.p7	17:29605800	CAATAATTTTCTCAT[C/T]GTTTATGGTGGCAGA	124930
rs115297703	snp	A/C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29599074	CAGTGGATAGAGCCA[A/C/T]AGCAGCTGTTACCTC	124930
rs115505409	snp	C/T	0.00914312	0.0669923	intron-variant	ANKRD13B	GRCh38.p7	17:29594783	CGCAGTTGCCCGCTG[C/T]GGGAATTTACCTTCT	124930
rs115688312	snp	C/G	0.0626037	0.165477	intron-variant	ANKRD13B	GRCh38.p7	17:29606985	AACCTGGGAGACGGA[C/G]GTTACAGCGAGCTGA	124930
rs115794994	snp	A/G	0.00914312	0.0669923	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29597718	ACTTACACTGCAGGC[A/G]GCACTCTGGGCTTGT	124930
rs115900863	snp	A/C	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29599077	TGGATAGAGCCATAG[A/C]AGCTGTTACCTCAGA	124930
rs116395945	snp	A/G	0.077417	0.180873	intron-variant	ANKRD13B	GRCh38.p7	17:29609664	GCAACCCTTTCTGGT[A/G]GGTGCTGTTCTGTTA	124930
rs116633125	snp	C/T	0.00993419	0.0697739	intron-variant	ANKRD13B	GRCh38.p7	17:29596170	CCCGCAGAGGCCCTC[C/T]GTGGGCAGGCTTGGC	124930
rs116634534	snp	A/G	0.00598423	0.0543719	intron-variant	ANKRD13B	GRCh38.p7	17:29609075	CCCCTGTGCTGTTCC[A/G]TGTCTGGCAGACACA	124930
rs117421059	snp	C/T	0.0197687	0.0974348	intron-variant	ANKRD13B	GRCh38.p7	17:29596825	GTAAGCTAGGAAGCT[C/T]GGGAGAGGGAGCCAC	124930
rs117566858	snp	A/G	0.0221141	0.102801	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29597899	TGGAGCCTGGAGCTG[A/G]GGCACCTGATGGGGA	124930
rs117661862	snp	C/T	0.0335799	0.125149	intron-variant	ANKRD13B	GRCh38.p7	17:29609328	CGGTGGGGTGCCTGC[C/T]TCACCTGGACCACTC	124930
rs117762713	snp	A/G	0.00318978	0.0398085	intron-variant	ANKRD13B	GRCh38.p7	17:29606230	AGTTCACTGTTCTTA[A/G]CCAGAAGTCCTAGAC	124930
rs138014603	snp	A/G	1.65195e-05	0.00287393	missense, downstream-variant-500B, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29612264	CCTCCTGGCTTCCCA[A/G]TTAAGATTGGTGAGA	124930
rs138062489	snp	C/T	0.00398564	0.0444627	intron-variant	ANKRD13B	GRCh38.p7	17:29611482	CCCCACCCCAGGAAC[C/T]GGCCTCCTCCCTAGG	124930
rs138152044	snp	C/T	0.00438332	0.0466095	intron-variant	ANKRD13B	GRCh38.p7	17:29603560	AGCCAACTTTATTTT[C/T]CAGTACTGTTTTTCT	124930
rs138222022	snp	C/T	0.000798403	0.0199641	intron-variant	ANKRD13B	GRCh38.p7	17:29600470	GGGGCTGGGGTTTCA[C/T]GGATCACTGGCTTTC	124930
rs138484452	snp	C/T	0.000798403	0.0199641	intron-variant, missense	ANKRD13B	GRCh38.p7	17:29594589	ACAGGTCACAGATTG[C/T]CACTTCTGCCCTTGG	124930
rs138638393	snp	C/G	4.96611e-05	0.00498278	missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29608913	AAGAGCGGCCAGAAC[C/G]TGAGGGTAGACACCA	124930
rs138672413	snp	C/T	0.00993419	0.0697739	intron-variant	ANKRD13B	GRCh38.p7	17:29597170	AAGCACTGTGTTTAG[C/T]CCATACATGAGATGT	124930
rs138719192	snp	A/G	3.51198e-05	0.0041903	missense, utr-variant-5-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29607769	CAGCTGGATCCCCGC[A/G]GCCGGACTCCCCTGC	124930
rs138885113	in-del	-/ACCTTGCC	0.0252325	0.109451	intron-variant	ANKRD13B	GRCh38.p7	17:29611105	GTAGAAAGTCAGGGG[-/ACCTTGCC]ACAGATTCTGTATGC	124930
rs139188920	snp	C/G			intron-variant	ANKRD13B	GRCh38.p7	17:29600034	GGCGCCCGCCACCAC[C/G]CCCAGCTAATTTTTT	124930
rs139305337	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29597677	AGATTAATGAATTCT[C/T]CTACCTGGGCCCAGG	124930
rs139389888	snp	C/T	0.00316293	0.0396417	synonymous-codon, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29609120	GGAGATTGACCACGA[C/T]CGCCGGGTGGTGTAC	124930
rs139413611	snp	A/G	0.00318978	0.0398085	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29599195	AGGATCCTGGAGAAC[A/G]TTCCGGGGAAGGCCA	124930
rs139479733	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29601609	GGATCATTTTCTTTC[C/T]ACCTGAAGAACTCCC	124930
rs139540682	snp	C/T	0.0569829	0.158885	intron-variant	ANKRD13B	GRCh38.p7	17:29601473	GTGACCTGCCCGCCT[C/T]GGCCTCCCAAAGTGC	124930
rs139544977	snp	A/G	0.00438332	0.0466095	intron-variant	ANKRD13B	GRCh38.p7	17:29606567	TGTCTCAAAAAACAA[A/G]CAAACAAACAAACAA	124930
rs139619456	in-del	-/GGGG			frameshift-variant, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29613514	AGCAGGAGGAGAGGC[-/GGGG]GGCGGCGCGCGCGCC	124930
rs139851635	snp	G/T			intron-variant	ANKRD13B	GRCh38.p7	17:29606109	TAGAGATGGGGTTTC[G/T]CCATGTTGTCAGGCT	124930
rs140086609	in-del	-/CA			intron-variant	ANKRD13B	GRCh38.p7	17:29609620	GGGCACGTGCACACG[-/CA]CACACACACACACAT	124930
rs140351736	snp	A/C	0.000430656	0.0146677	synonymous-codon, missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29611977	CCGTGATATGGGCCG[A/C]CCCATGGAACTGACC	124930
rs140421720	snp	A/C	0.00358779	0.0422022	intron-variant	ANKRD13B	GRCh38.p7	17:29610417	GAGATTGTAAGTCTC[A/C]GGAGGGCAGGGATCA	124930
rs140506698	snp	A/G	0.000100194	0.0070772	missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29610703	TATGGGGCATCTAAC[A/G]TGGAGCTCATCACCC	124930
rs140528270	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29602719	GACCCTTTTTTGAAA[C/T]AAGGTCTCATTCATA	124930
rs140730026	snp	A/G	0.00358779	0.0422022	upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29592401	TGAGAGGCCAATTCA[A/G]CTTTTACCACACCCT	124930
rs141001115	snp	A/G	0.0123036	0.0774623	intron-variant	ANKRD13B	GRCh38.p7	17:29602468	AGATGTTGGCAGGGT[A/G]GCAGTCCTTCCAAAG	124930
rs141232549	snp	G/T	0.00119737	0.0244387	intron-variant	ANKRD13B	GRCh38.p7	17:29603246	TAATGTCTTACAGAT[G/T]ATGAGGCTCCATAGA	124930
rs141243340	snp	A/G	0.0581099	0.160244	intron-variant	ANKRD13B	GRCh38.p7	17:29604691	GGATTACAGGCACCC[A/G]TCACCAAGCCCGGCT	124930
rs141285986	snp	A/G	0.00398564	0.0444627	intron-variant	ANKRD13B	GRCh38.p7	17:29609695	GTATTCCCATTTTAC[A/G]CATGTTTATTGAGTC	124930
rs141435253	snp	A/G	0.000798403	0.0199641	intron-variant	ANKRD13B	GRCh38.p7	17:29596319	GGTGCCTGGTGAAGG[A/G]AAGGGGCACCCAGCA	124930
rs141666210	snp	C/T	0.000241109	0.0109771	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29608086	GCTGGCGGGCATCCC[C/T]GTGCTCCTGGAGAAG	124930
rs141834188	snp	A/G	0.00517822	0.0506191	intron-variant, utr-variant-5-prime	ANKRD13B	GRCh38.p7	17:29594398	GGGGCCCTGGCTGCT[A/G]GAAGGACTTGAGGTT	124930
rs141839830	snp	A/C/T	0.0023933	0.0345097	intron-variant	ANKRD13B	GRCh38.p7	17:29597291	GTTCCTGTGCAAATA[A/C/T]GCACACACACGTTAC	124930
rs142075575	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29599071	GGGCAGTGGATAGAG[A/C]CATAGCAGCTGTTAC	124930
rs142430364	snp	G/T			intron-variant	ANKRD13B	GRCh38.p7	17:29602549	CACAACCCTCTTGGC[G/T]TGTGGCTGCAGAACT	124930
rs142490734	snp	A/C	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29595428	GAATGCCTCAGTCCC[A/C]CTCCCTTGCCTGAGG	124930
rs142597451	snp	C/G	0.00119737	0.0244387	intron-variant	ANKRD13B	GRCh38.p7	17:29601162	CTCCTGGGCTCAAGT[C/G]ATCTGCCCACCTCGG	124930
rs142904329	snp	A/G	0.000373914	0.0136681	intron-variant	ANKRD13B	GRCh38.p7	17:29609314	CCCTTGAGCCAGCCC[A/G]GTGGGGTGCCTGCCT	124930
rs143163561	snp	A/G	0.00119737	0.0244387	intron-variant	ANKRD13B	GRCh38.p7	17:29604025	GGATTACAGGCTCAC[A/G]TGAGCCACCGCACCC	124930
rs143366280	snp	C/T	1.67713e-05	0.00289575	synonymous-codon, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29609093	TCTGGCAGACACAAG[C/T]GCCGTGGTCATGGAG	124930
rs143448815	snp	C/G	0.0267878	0.112589	intron-variant	ANKRD13B	GRCh38.p7	17:29606593	AACAAACAAAACTTA[C/G]GTTTAACAAACATGC	124930
rs143524581	snp	A/G	0.000153988	0.00877328	missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29610712	TCTAACGTGGAGCTC[A/G]TCACCCGCACACGGA	124930
rs143637888	snp	C/G	0.000798403	0.0199641	intron-variant	ANKRD13B	GRCh38.p7	17:29609860	AGTTGGGGTTCAGAT[C/G]CTGGCTGGCCTGACC	124930
rs143677360	snp	A/G	0.00119737	0.0244387	intron-variant	ANKRD13B	GRCh38.p7	17:29600410	GGTAGATAGGGTGGT[A/G]GTGGTGTGACCTGGC	124930
rs143781424	in-del	-/A	0.00914312	0.0669923	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29597457	TGCCTGAGTGGAGGT[-/A]AGGGAGGCTCTCTGC	124930
rs143960252	snp	A/C	0.00716266	0.059414	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29598690	AGGAGCTAGGACTAC[A/C]GGTGGTGCCACCATG	124930
rs144081842	snp	C/T	0.0111196	0.0737302	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29598081	GCCCTCTCCCACTCC[C/T]GCTGCCGGGCTCAGG	124930
rs144323477	snp	A/C/G/T	0.000438492	0.0148008	synonymous-codon, missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29609166	CTGGCTGGGCAGGAC[A/C/G/T]GGGAGCTGCTGCTGG	124930
rs144471450	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29601592	ATTCAAGTTTCTATC[C/T]GGGATCATTTTCTTT	124930
rs144781865	snp	A/C			intron-variant	ANKRD13B	GRCh38.p7	17:29606119	GTTTCTCCATGTTGT[A/C]AGGCTGGTCTCGAAC	124930
rs144969418	snp	G/T	0.0569829	0.158885	intron-variant	ANKRD13B	GRCh38.p7	17:29603299	CAGGCTGGAGTGCAG[G/T]GGCGTGATCATAGCT	124930
rs144992907	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29602003	TGGTGTAGTTTACTT[C/T]GTGTTTGTCTTACTT	124930
rs145581152	snp	A/C	0.0577344	0.159793	intron-variant	ANKRD13B	GRCh38.p7	17:29600944	TTTTTTTTTTTTTTG[A/C]GACAGGGTCTGGCTT	124930
rs145777071	snp	C/T	0.0111196	0.0737302			GRCh38.p7	17:29599977	CGCCTCCCGGGTTCA[C/T]ACCATTCTCCTGCCT	124930
rs145870428	snp	C/T	0.00252555	0.0354457	synonymous-codon, downstream-variant-500B, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29612418	AATCCCGATCTTCCA[C/T]ATCCTCAACGCCCGC	124930
rs145883028	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29593044	TCTTCGGCCACCTGC[C/T]ACCCCCAGTTTCACG	124930
rs146259821	snp	C/T	0.0138799	0.0821421	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29597549	TGGGATAAGGAATCT[C/T]CGTTCTCTTGGTGGG	124930
rs146568401	snp	A/G	0.00318978	0.0398085	intron-variant	ANKRD13B	GRCh38.p7	17:29603139	CAGGCGTGAGCCACC[A/G]CACCCGGCCTATTTC	124930
rs146587445	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29609533	CAGAAGCAATGCAGC[A/G]TGGTCAAGCACTTAT	124930
rs146596993	snp	C/T	0.0170251	0.090679	intron-variant	ANKRD13B	GRCh38.p7	17:29595519	TCTCCAGCAGGCCTC[C/T]CTGCTGATAATCCTG	124930
rs146784185	snp	C/T	0.000798403	0.0199641	intron-variant	ANKRD13B	GRCh38.p7	17:29610400	TTTATTGTCTCCTTA[C/T]AGAGATTGTAAGTCT	124930
rs146795223	snp	G/T	3.36961e-05	0.0041045	missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29609385	CCTGGGCTGGCGCAG[G/T]GAAAAGACGGAGATG	124930
rs146978452	snp	C/T	0.00159617	0.0282053	intron-variant	ANKRD13B	GRCh38.p7	17:29611312	ACTGTCCAGGGTCAC[C/T]GAGCTGGAGAGGAGC	124930
rs147140187	snp	C/G	0.00517822	0.0506191	intron-variant	ANKRD13B	GRCh38.p7	17:29607645	GAGCAGCCCCAGCAG[C/G]GGGTGGGGGTTGCTG	124930
rs147149998	snp	C/T	9.94909e-05	0.00705235	synonymous-codon, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29608879	CAAGATCTGCCCTAG[C/T]GACACCTACAAAGTG	124930
rs147156385	snp	A/C/G	0.00161583	0.0283783	synonymous-codon, downstream-variant-500B, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29612409	ATCCTCAGAAATCCC[A/C/G]ATCTTCCACATCCTC	124930
rs147534314	snp	A/C/G	0.000150877	0.00868433	missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29609097	GCAGACACAAGCGCC[A/C/G]TGGTCATGGAGATTG	124930
rs147677310	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29606118	GGTTTCTCCATGTTG[C/T]CAGGCTGGTCTCGAA	124930
rs147738152	snp	C/G	0.0162398	0.0886349	intron-variant	ANKRD13B	GRCh38.p7	17:29599858	CTGGGTTCTTAGCAT[C/G]TAATTTGTTTTTTTT	124930
rs147754766	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29602027	CTTACTTGGGGTTCA[C/T]TGAATTTCTTGGTTC	124930
rs148007819	snp	C/T	0.000267134	0.011554	missense, utr-variant-5-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29608039	GTGCAGCTGGTGCTT[C/T]GGTACCGGGACTACC	124930
rs148193762	snp	A/G	0.0166325	0.0896639	utr-variant-3-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29613782	GCCAGGGCCCTGGAG[A/G]CAACTGGCACGGCCT	124930
rs148247479	snp	A/G	0.0162398	0.0886349	intron-variant	ANKRD13B	GRCh38.p7	17:29604245	ACAGAGTCTTGCTCT[A/G]TCACCCAGGCTTGAG	124930
rs148316748	snp	G/T	0.000798403	0.0199641	intron-variant	ANKRD13B	GRCh38.p7	17:29596301	AGTGATGGGCAGATA[G/T]GAGGTGCCTGGTGAA	124930
rs148565151	snp	A/G	5.08066e-05	0.00503991	intron-variant	ANKRD13B	GRCh38.p7	17:29609294	GGTGGACATGGCCTT[A/G]GTCACCCTTGAGCCA	124930
rs148747929	snp	C/T	0.000285986	0.0119545	synonymous-codon, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29609225	GCTGAGCCGGCTTAC[C/T]GCGCCCGTCGTCACC	124930
rs148873780	snp	A/G	0.00168032	0.0289368	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29607834	CCGTGTGCTCCTGGC[A/G]CACGGCGCAGACGTG	124930
rs148886113	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29610889	ATGCTTTATTCAGGC[C/T]GATAGATTTCAATTC	124930
rs148954809	snp	C/T	0.0513262	0.151752	intron-variant	ANKRD13B	GRCh38.p7	17:29600155	AGCTGGGATTACAGG[C/T]GTGAGCCACTGCACC	124930
rs149274095	snp	A/G	0.00358779	0.0422022	intron-variant	ANKRD13B	GRCh38.p7	17:29601582	CTTTGTACAGATTCA[A/G]GTTTCTATCTGGGAT	124930
rs149535620	snp	A/G	0.000798403	0.0199641	intron-variant	ANKRD13B	GRCh38.p7	17:29603643	TTTAAATTGTGCAGT[A/G]TCTAATCTGCTGTTA	124930
rs149562910	in-del	-/AG	0.00557542	0.0525036	utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant	CORO6, ANKRD13B	GRCh38.p7	17:29615161	CGGTGGAAAGAAGGA[-/AG]AGAGTTCTCTACCAC	124930
rs149853652	snp	A/G	0.000798403	0.0199641	intron-variant	ANKRD13B	GRCh38.p7	17:29608671	TCCCGACCTCAGGTT[A/G]CTCTTCTGTGTGAGT	124930
rs150036930	snp	A/T	0.000153988	0.00877328	missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29609142	GTGGTGTACACAGAG[A/T]CTCTGGCACTGGCTG	124930
rs150172789	snp	G/T	0.00676609	0.0577691	intron-variant	ANKRD13B	GRCh38.p7	17:29610541	AATGAATGAATGAAT[G/T]ACCTCATATATTCAC	124930
rs150249107	in-del	-/TGGGAGCGGGCCCTGCCCGC/TGGGAGCGGGCCCTGCCCGCT	0.495868	0.0452663	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29593895	ACCGGGAAAGGGTGA[lengthTooLong]TCCCCTCCGGCCGGG	124930
rs150355023	snp	A/G	6.59337e-05	0.0057413	synonymous-codon, utr-variant-3-prime, intron-variant, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29612161	GCATCCCCTGTCCCT[A/G]TGTGAGCAGGTGGCC	124930
rs150429632	snp	C/G	0.00438332	0.0466095	intron-variant	ANKRD13B	GRCh38.p7	17:29603002	ACTACAGGTGCCCAC[C/G]ACCACGCCTGGCTAA	124930
rs150749605	snp	C/T	0.00597247	0.0543191	intron-variant	ANKRD13B	GRCh38.p7	17:29606387	AACATATCAAAACCC[C/T]GTCTCTACTAAAATA	124930
rs150908445	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant	CORO6, ANKRD13B	GRCh38.p7	17:29615033	TCTGAGAGAGGCAAC[A/G]GCAGAGGGTTGGGGG	124930
rs150944594	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29592217	GGTAGTATCTAGATT[C/T]TCATTTTGAAGGGGA	124930
rs180717079	snp	A/G	0.00119737	0.0244387	intron-variant	ANKRD13B	GRCh38.p7	17:29605814	TTGTTTATGGTGGCA[A/G]AGTAATTTCATTTAT	124930
rs180720298	snp	A/C	0.00279162	0.0372561	intron-variant	ANKRD13B	GRCh38.p7	17:29594849	GAGGAGCTGTGCAAT[A/C]GCCAAGGGAAGCATG	124930
rs181260354	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29604655	CAAGTGATTCTTGTG[C/T]CTCAGCCTCCTGAGT	124930
rs181271605	snp	C/G	0.00159617	0.0282053	intron-variant	ANKRD13B	GRCh38.p7	17:29595750	GCCAGGGGGAATATA[C/G]GGCACTGGTGGAGGT	124930
rs181293455	snp	C/T	0.000367181	0.0135446	intron-variant	ANKRD13B	GRCh38.p7	17:29612042	GGGAAGGTGGGGGGC[C/T]GGGGCTCCAGGAGAT	124930
rs181501222	snp	C/T	0.00199481	0.0315187	intron-variant	ANKRD13B	GRCh38.p7	17:29601084	ATGCACCACCACGCC[C/T]GGCTAATTTTAGTAT	124930
rs181518764	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29610047	AATACAAAAAATTAG[C/T]CGGGTGTGGTAGCAG	124930
rs181554868	snp	G/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29599411	CAAAGAGGCAGTAGG[G/T]GGCTGCCAGTGAGAG	124930
rs182000166	snp	A/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29604720	CTAATTTTTTGTATT[A/T]TTAGTAGAGATGTGG	124930
rs182094305	snp	C/T	0.00279162	0.0372561	intron-variant	ANKRD13B	GRCh38.p7	17:29596558	AGGGACATGTGTGGG[C/T]TGGGCCTGGGGAGCA	124930
rs182387453	snp	G/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29610302	GTGTGGCATCTCCTC[G/T]GAAAGCCTCCCCTGC	124930
rs182494843	snp	A/C	0.00159617	0.0282053	intron-variant	ANKRD13B	GRCh38.p7	17:29606159	CAGGTGATCTACCCG[A/C]CTCGGCCTCCCAAAG	124930
rs182723230	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29602952	CCCTTCCCGGGTTCA[A/G]GCGATTCTCCTGCCT	124930
rs182913922	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29597836	GTGCTCCTGAGGTGT[A/G]GGGATGGGGAGGAGC	124930
rs183288956	snp	A/C			downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	CORO6, ANKRD13B	GRCh38.p7	17:29614745	TGAGGCACAAATAAA[A/C]GAGGCTTCATACCGG	124930
rs183331448	snp	A/C	0.00159617	0.0282053	intron-variant	ANKRD13B	GRCh38.p7	17:29601622	TCCACCTGAAGAACT[A/C]CCTTTAACATTTCCT	124930
rs183349614	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29602322	ATGGCGTGAACCGGG[A/G]AAGCGGAGCTTACAG	124930
rs183507891	snp	A/C			intron-variant	ANKRD13B	GRCh38.p7	17:29596508	TCCCTGGGGTGGGAA[A/C]AGGGGGAAGGGTTAG	124930
rs183797622	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29599363	AGCTGCCATAGGTGA[A/G]GTGGACAATAGAGCC	124930
rs184527223	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29607149	TTATTCACAAAATTA[C/T]AGGATTTGTACAAAT	124930
rs184617534	snp	C/T	0.00279162	0.0372561	upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29592614	GGACCATCTTTCCCG[C/T]GTTACTGGACATTCT	124930
rs184680227	snp	G/T	0.0023933	0.0345097	intron-variant	ANKRD13B	GRCh38.p7	17:29604676	CCTCCTGAGTAGCTG[G/T]GATTACAGGCACCCA	124930
rs184761410	snp	C/T	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29598398	CAGTGCTCCTTGCTC[C/T]GCCTCTCCCACCTCC	124930
rs184957348	snp	A/G	0.00279162	0.0372561	intron-variant	ANKRD13B	GRCh38.p7	17:29604113	TTGGACATTGTAAAT[A/G]TGATGTTAAGCATCT	124930
rs185234037	snp	A/G	0.0023933	0.0345097	intron-variant	ANKRD13B	GRCh38.p7	17:29610907	TAGATTTCAATTCAG[A/G]TGCCAAGCCCTAAGG	124930
rs185362222	snp	C/T	0.00119737	0.0244387	utr-variant-3-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29613960	CCGCATTTCTGTTCA[C/T]TAACCCCACTCCAGG	124930
rs185468167	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29592330	GACATCACAGTCCCC[C/T]CCCTCCAGGGACTGG	124930
rs185497920	snp	A/G	0.00119737	0.0244387	intron-variant	ANKRD13B	GRCh38.p7	17:29603926	TCTGTTGCCCAGGCT[A/G]GAGTGCAGGGGCGCC	124930
rs185512758	snp	A/G	0.00119737	0.0244387	intron-variant	ANKRD13B	GRCh38.p7	17:29595376	GGAAGAACTTCCCAG[A/G]GGTCCAAGGATCACT	124930
rs185722910	snp	G/T	0.00159617	0.0282053	intron-variant	ANKRD13B	GRCh38.p7	17:29610057	ATTAGCCGGGTGTGG[G/T]AGCAGGCGCCTGTAA	124930
rs186213475	snp	C/G	0.00159617	0.0282053	intron-variant	ANKRD13B	GRCh38.p7	17:29601623	CCACCTGAAGAACTC[C/G]CTTTAACATTTCCTG	124930
rs186272462	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29599938	CTAGAGTGCAGTGGC[A/G]CAATCTCGGCTCACT	124930
rs186356389	snp	C/T	0.00119737	0.0244387	intron-variant	ANKRD13B	GRCh38.p7	17:29596537	AGCCTGTGCAGCTCC[C/T]GTGGGAGGGACATGT	124930
rs186440646	snp	C/G	0.00358779	0.0422022	intron-variant	ANKRD13B	GRCh38.p7	17:29601429	GTTTCACCATGTTGG[C/G]CAGGCTGGTCTCAAA	124930
rs186566626	snp	A/G	0.00199481	0.0315187	intron-variant	ANKRD13B	GRCh38.p7	17:29605893	GAAGAGGAGGGAGTT[A/G]CATGCATGTGGTCAG	124930
rs186745243	snp	A/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29607532	TGTCTTCTAAGCCCC[A/T]TTCCATCCACGTGTC	124930
rs187069208	snp	A/G	0.00636936	0.0560724	intron-variant	ANKRD13B	GRCh38.p7	17:29605065	TTTCACTATACACAT[A/G]TGAAGTTTAGTATTC	124930
rs187135994	snp	A/C	0.000798403	0.0199641	intron-variant	ANKRD13B	GRCh38.p7	17:29596114	CCAGGTTTCCCTGGT[A/C]TTGGCTTGGCATAGC	124930
rs187357118	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29603214	GGATTCCAATAGATA[C/T]ATGTTACAATGCTTG	124930
rs187417457	snp	A/G	0.00716266	0.059414	utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant	CORO6, ANKRD13B	GRCh38.p7	17:29615166	GAAAGAAGGAAGAGA[A/G]TTCTCTACCACAGAC	124930
rs187490023	snp	A/G	0.00358779	0.0422022	intron-variant	ANKRD13B	GRCh38.p7	17:29606201	CAGGCGTGAGCTACC[A/G]CGCCTGGCCTGTCAG	124930
rs187575699	snp	A/G	0.00835141	0.0640778	intron-variant	ANKRD13B	GRCh38.p7	17:29596884	TCTGGGATGAGGGGG[A/G]GGGGCTGCAAGGGCA	124930
rs187845047	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29602469	GATGTTGGCAGGGTG[A/G]CAGTCCTTCCAAAGG	124930
rs187988479	snp	C/G	0.00119737	0.0244387	intron-variant	ANKRD13B	GRCh38.p7	17:29603927	CTGTTGCCCAGGCTG[C/G]AGTGCAGGGGCGCCA	124930
rs188240668	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29594648	CAGAGATGACCCCCC[A/G]CCTCCAGGGTGGGCT	124930
rs188527468	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29604603	CCAGAGTGTAGTGGT[A/G]CAGTCTTGGCTCACT	124930
rs188651449	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29606536	GCACTCTAGCCTGGG[C/T]GACACAGTGAGACTC	124930
rs188767262	snp	C/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29597877	CAAGGAAGTGCCAGC[C/G]GCTCTCTGGAGCCTG	124930
rs189004725	snp	C/G/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29604696	ACAGGCACCCATCAC[C/G/T]AAGCCCGGCTAATTT	124930
rs189137329	snp	A/C			intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29599370	ATAGGTGAGGTGGAC[A/C]ATAGAGCCTGGCAAC	124930
rs189154384	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29609765	GGAAGTAGGGATGAT[C/T]GGTCCATTTTATGAT	124930
rs189657752	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29611128	ACAGATTCTGTATGC[C/T]CATTGATGCCACACC	124930
rs189667363	snp	A/G	0.00398564	0.0444627	intron-variant	ANKRD13B	GRCh38.p7	17:29595664	CAGAAACAAGGTCCC[A/G]GATTCACCCCTACCC	124930
rs189919035	snp	C/T	0.000798403	0.0199641	intron-variant	ANKRD13B	GRCh38.p7	17:29596548	CTCCCGTGGGAGGGA[C/T]ATGTGTGGGCTGGGC	124930
rs189940941	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29592549	CACCTGCTGCTTTTT[A/C]TGTCCAACCTCACTC	124930
rs190199352	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29610277	AACTAACAAATGCCA[C/T]GGGTTTTGTGTGTGG	124930
rs190294059	snp	A/G	0.00119737	0.0244387	intron-variant	ANKRD13B	GRCh38.p7	17:29606070	GGCATGGGCCACCAC[A/G]CCTGGCTAATTTTGT	124930
rs190336666	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29600379	TTCTGAGGTCTTTGG[A/G]ACAACTTCCTACTCG	124930
rs190420610	snp	C/T	0.0275645	0.114116	intron-variant	ANKRD13B	GRCh38.p7	17:29606415	ATACAAAAATTAGCC[C/T]GGCATAGTGGTGCTC	124930
rs190535245	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29602686	TCTTGAGATCCTTAA[C/T]TTAATTATGTCTGCA	124930
rs190570300	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29614188	CTCAGGGTGGTTCCA[C/G]CTTCTCCTTGGGCAG	124930
rs190690194	snp	G/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29602088	CAAATTACTACAAAC[G/T]AGGTGGGTTAAAACA	124930
rs191087020	snp	A/C	0.00119737	0.0244387	intron-variant	ANKRD13B	GRCh38.p7	17:29605812	CATTGTTTATGGTGG[A/C]AGAGTAATTTCATTT	124930
rs191205288	snp	A/C			intron-variant	ANKRD13B	GRCh38.p7	17:29601556	TTAACATTTTTTGGC[A/C]CTCTTCAATCCTTTG	124930
rs191295983	snp	C/T	0.0126979	0.078662	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29599194	GAGGATCCTGGAGAA[C/T]GTTCCGGGGAAGGCC	124930
rs191525020	snp	C/T	0.00279162	0.0372561	intron-variant	ANKRD13B	GRCh38.p7	17:29596391	TGTTCTCTGCCAGGT[C/T]GGGGGGGACAGGGTT	124930
rs191886582	snp	A/G	0.000397463	0.0140916	intron-variant	ANKRD13B	GRCh38.p7	17:29608186	GCCTCTCTCCCCTTC[A/G]TCCTCCAGGCCCAGG	124930
rs191964828	snp	A/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29598082	CCCTCTCCCACTCCC[A/G]CTGCCGGGCTCAGGA	124930
rs192086816	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant	CORO6, ANKRD13B	GRCh38.p7	17:29615196	CCGCTGTGGGTGTAG[C/T]CACTGGGTCCGGCTC	124930
rs192219068	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29603963	GCTCACTGCAAGCTC[A/G]ATCTCCTGACCTCGT	124930
rs192670509	snp	A/T	0.00119737	0.0244387	intron-variant	ANKRD13B	GRCh38.p7	17:29603925	CTCTGTTGCCCAGGC[A/T]GGAGTGCAGGGGCGC	124930
rs192739545	snp	A/G	0.0138799	0.0821421	intron-variant	ANKRD13B	GRCh38.p7	17:29606715	GGGTGACATAGTGAG[A/G]CCCTGTCTCAAGTAA	124930
rs192989543	snp	A/G			intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29597573	TGGTGGGGAGGGCTG[A/G]GTGTTGGGTTTCATG	124930
rs193286639	snp	C/T	0.00159617	0.0282053	upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29592552	CTGCTGCTTTTTCTG[C/T]CCAACCTCACTCTGG	124930
rs199606091	in-del	-/TA			intron-variant	ANKRD13B	GRCh38.p7	17:29605472	ACACACACGCATATG[-/TA]TATATATATATTTGA	124930
rs199706963	snp	A/G	0.000580821	0.0170315	intron-variant	ANKRD13B	GRCh38.p7	17:29609008	AGGTCAGGCAGGCAG[A/G]AAGTGGGGCAGGGTG	124930
rs199779863	snp	C/G	0.0010923	0.0233443	missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29613535	CGCGCGCGCCAGGAG[C/G]AGGAGGAGCTGGAGC	124930
rs199786495	snp	C/T	0.000157766	0.00888021	missense, upstream-variant-2KB, intron-variant, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29593671	CCGAGGGCAAGTATC[C/T]GCTGCACTACCTCGT	124930
rs199786725	snp	C/T	1.68821e-05	0.0029053	missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29609393	GGCGCAGTGAAAAGA[C/T]GGAGATGGTGAATGG	124930
rs199911781	snp	A/G	1.65367e-05	0.00287543	intron-variant	ANKRD13B	GRCh38.p7	17:29611693	ATGTGGATGTGGCTC[A/G]GGAGGAGGCTTGGGA	124930
rs199997513	snp	C/G/T	0.0380707	0.132614	missense, utr-variant-5-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29608076	TGGTGAAGCGGCTGG[C/G/T]GGGCATCCCCGTGCT	124930
rs200009445	snp	C/T	0.00299549	0.0385846	intron-variant	ANKRD13B	GRCh38.p7	17:29607902	CCTGCTCACCCCAGC[C/T]CCACAGCCGGGGCCT	124930
rs200129442	in-del	-/A			intron-variant	ANKRD13B	GRCh38.p7	17:29601765	CATACTGGATTAGAG[-/A]AAAAAAAAAAAAGAA	124930
rs200188306	in-del	-/G	0.0170251	0.090679	intron-variant, utr-variant-5-prime	ANKRD13B	GRCh38.p7	17:29594265	CCCAGCCCCAGCTCA[-/G]GAACAGGGAGTGGAG	124930
rs200201604	snp	C/T	5.00171e-05	0.0050006	intron-variant	ANKRD13B	GRCh38.p7	17:29608261	CGGGCTGCAGCAGGT[C/T]GCTTCTGGGCTCTCC	124930
rs200279578	snp	C/T	4.92393e-05	0.00496157	synonymous-codon, downstream-variant-500B, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29612710	CCCGCGCGGCTACAG[C/T]ATGATGGGCGGCCAG	124930
rs200339501	in-del	-/GAG			intron-variant	ANKRD13B	GRCh38.p7	17:29607348	CCCTTAGGGTAGGTC[-/GAG]TGGTCCCAGGTGAGC	124930
rs200348157	snp	A/C			intron-variant	ANKRD13B	GRCh38.p7	17:29605417	ATATACACACACAAA[A/C]ACACACACACACACA	124930
rs200525661	in-del	-/CAGA	0.00914312	0.0669923	utr-variant-3-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29613639	CCCAGGGCCAGGAGC[-/CAGA]CAAACCCCGGCCTGC	124930
rs200671034	snp	C/T	1.68272e-05	0.00290057	synonymous-codon, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29609261	GCTTGACACCAAGAA[C/T]ATCTCCTTTGAGAGG	124930
rs200745766	snp	A/C	0.000124293	0.00788233	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612565	CACGAGTGAGGCCCC[A/C]CGCGAGAACGCCTGC	124930
rs200959557	snp	A/C	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29607053	AGACTCCGTCCCCCC[A/C]AAAAAAACACAAAAA	124930
rs200991847	snp	C/T	0.000123024	0.00784199	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29607768	GCAGCTGGATCCCCG[C/T]GGCCGGACTCCCCTG	124930
rs201124075	snp	C/T	4.95397e-05	0.00497668	synonymous-codon, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29611625	AATCGCTGAGCAGCA[C/T]GGGGGCCCCCAAAAT	124930
rs201249702	in-del	-/A			intron-variant	ANKRD13B	GRCh38.p7	17:29607052	AGACTCCGTCCCCCC[-/A]AAAAAAAACACAAAA	124930
rs201268799	snp	A/G	1.68168e-05	0.00289967	intron-variant	ANKRD13B	GRCh38.p7	17:29608137	CCTCTCAGCCTCCAC[A/G]GGAGCCCTTGAGCCC	124930
rs201309202	snp	A/G	0.000306166	0.0123689	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612358	GGCTGAGGCTGAGGT[A/G]TGAGGGGCTGAGTGG	124930
rs201590854	snp	C/T	0.000133425	0.00816667	intron-variant	ANKRD13B	GRCh38.p7	17:29609042	ACGATGGGAGGCAGC[C/T]CCAGGCCACCCCTGA	124930
rs201684708	snp	C/T	0.00506326	0.0500599	intron-variant	ANKRD13B	GRCh38.p7	17:29609466	AGCTGCACTCTTGCC[C/T]ACAGCAAGCTGTACA	124930
rs201911935	snp	G/T	1.80595e-05	0.0030049	intron-variant	ANKRD13B	GRCh38.p7	17:29607728	TTTATCTTCCACTCC[G/T]CCTCCTCCTCCAGGT	124930
rs201968159	snp	A/C/G	0	0	intron-variant	ANKRD13B	GRCh38.p7	17:29607685	GGGCTGTCTGGCTCC[A/C/G]GAGGGCTGCCTCCGA	124930
rs202011846	in-del	-/CAAA			intron-variant	ANKRD13B	GRCh38.p7	17:29606587	AAACAAACAAACAAA[-/CAAA]ACTTACGTTTAACAA	124930
rs202186985	snp	C/T	7.19683e-05	0.00599825	intron-variant	ANKRD13B	GRCh38.p7	17:29607896	GGCAGCCCTGCTCAC[C/T]CCAGCCCCACAGCCG	124930
rs202213583	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612356	GGGGCTGAGGCTGAG[A/G]TGTGAGGGGCTGAGT	124930
rs367551105	snp	C/G	0.000153988	0.00877327	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612882	ACGCCCACGCCTCCC[C/G]GCAGGTCACCATCTG	124930
rs367578278	snp	C/T	0.000569827	0.0168698	intron-variant	ANKRD13B	GRCh38.p7	17:29610657	AAGACCAGAACTGCT[C/T]ATGAGCCCTTTCTTC	124930
rs367658953	snp	A/G	1.88589e-05	0.00307068	intron-variant	ANKRD13B	GRCh38.p7	17:29610642	GGTAAGACACAGGGT[A/G]AGACCAGAACTGCTT	124930
rs367990384	snp	C/T	3.33084e-05	0.00408082	synonymous-codon, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29610711	ATCTAACGTGGAGCT[C/T]ATCACCCGCACACGG	124930
rs367994677	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29613349	CATTCCTTCCCCACC[C/T]CCAGGAGCGCCCCGC	124930
rs368106806	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29599970	CAAGCTCCGCCTCCC[A/G]GGTTCACACCATTCT	124930
rs368225471	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29609766	GAAGTAGGGATGATC[A/G]GTCCATTTTATGATG	124930
rs368295187	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29604119	ATTGTAAATATGATG[C/T]TAAGCATCTGGATTT	124930
rs368597241	snp	A/G	1.68895e-05	0.00290593	intron-variant	ANKRD13B	GRCh38.p7	17:29609286	GAGAGGTGGGTGGAC[A/G]TGGCCTTGGTCACCC	124930
rs368667865	snp	A/G	4.95356e-05	0.00497648	synonymous-codon, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29611622	GGGAATCGCTGAGCA[A/G]CACGGGGGCCCCCAA	124930
rs368732176	snp	C/T			intron-variant, synonymous-codon	ANKRD13B	GRCh38.p7	17:29594543	CATGCTTCAGGATGT[C/T]TTCTGGCCATGCTTC	124930
rs368970918	snp	C/T	1.75302e-05	0.00296054	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29607780	CCGCGGCCGGACTCC[C/T]CTGCACCTGGCCACC	124930
rs369145197	snp	C/T	0.00358779	0.0422022	intron-variant	ANKRD13B	GRCh38.p7	17:29606153	CAACCTCAGGTGATC[C/T]ACCCGCCTCGGCCTC	124930
rs369225050	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29604164	AAGAGTGTTGGGCTT[C/T]GTTCAGGCAGACTAG	124930
rs369275090	snp	A/G	1.6661e-05	0.00288621	intron-variant	ANKRD13B	GRCh38.p7	17:29612021	AGTGAGGCCCCTGCC[A/G]GTGCTGGGAAGGTGG	124930
rs369494016	snp	C/T	0.000414859	0.0143964	intron-variant	ANKRD13B	GRCh38.p7	17:29607958	GCTGAAGGGTCCTGC[C/T]CTGTGACCTTGCCTC	124930
rs369742035	snp	A/G			intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29597700	GGCCCAGGGCAAGGT[A/G]CCACTTACACTGCAG	124930
rs369846246	snp	A/G	3.36922e-05	0.00410426	synonymous-codon, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29609355	ACTCTGCTTCCCCAG[A/G]AACAAGACTGGCATC	124930
rs369866283	snp	A/G	0.00119737	0.0244387	intron-variant	ANKRD13B	GRCh38.p7	17:29602118	AACAAATATTTGGCC[A/G]GGTGTGGTGGCTCAC	124930
rs369982555	snp	C/G			intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29598388	TAATGAAAAGCAGTG[C/G]TCCTTGCTCCGCCTC	124930
rs370033767	snp	A/C/G	7.38789e-05	0.0060774	intron-variant	ANKRD13B	GRCh38.p7	17:29607702	AGGGCTGCCTCCGAC[A/C/G]TGACTGGGGCTTTAT	124930
rs370135938	in-del	-/T	0	0	intron-variant	ANKRD13B	GRCh38.p7	17:29607072	AAGCTTTTTTTGGGG[-/T]TTTTTTTTTGTGTTT	124930
rs370348552	snp	A/T	0.000566683	0.0168232	intron-variant	ANKRD13B	GRCh38.p7	17:29610668	TGCTTATGAGCCCTT[A/T]CTTCATCTGTCCCCA	124930
rs370396715	snp	A/G			intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29594030	GTGTCGGTGTTCCAT[A/G]TGGTGGGAGAGTCCG	124930
rs370416808	snp	C/G/T	5.04684e-05	0.00502315	synonymous-codon, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29609231	CCGGCTTACCGCGCC[C/G/T]GTCGTCACCACTCAG	124930
rs370492389	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29605224	CTCAGGAAGAGCACC[A/G]TGCTCTGCTCGGGCT	124930
rs370546318	snp	C/T			intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29598077	TGTGGCCCTCTCCCA[C/T]TCCCGCTGCCGGGCT	124930
rs370548766	in-del	-/AAAAA			intron-variant	ANKRD13B	GRCh38.p7	17:29606756	AAAAAAAAAAAAAAA[-/AAAAA]TCTTTTGTCTGGGCA	124930
rs370617698	snp	A/G	5.34202e-05	0.00516791	intron-variant	ANKRD13B	GRCh38.p7	17:29607922	AGCCGGGGCCTCCCC[A/G]GCATCATAGACCTAT	124930
rs370723205	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29610427	GTCTCAGGAGGGCAG[A/G]GATCATGTTTGGCTT	124930
rs370819588	snp	A/G	5.06034e-05	0.00502983	missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29609167	TGGCTGGGCAGGACC[A/G]GGAGCTGCTGCTGGC	124930
rs371147023	snp	G/T	0.00398564	0.0444627	intron-variant	ANKRD13B	GRCh38.p7	17:29595600	CCGCTGCAGGTAGAG[G/T]TGTTGGGGGCTGCTC	124930
rs371201901	snp	A/G	0.00517822	0.0506191	intron-variant	ANKRD13B	GRCh38.p7	17:29605712	GGGCTCAAGCAATCC[A/G]CCAACCTTTGCCTCC	124930
rs371236478	snp	A/C	4.94972e-05	0.00497455	missense, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29612243	GACTTCATCACCCTG[A/C]GTCTGCCTCCTGGCT	124930
rs371351432	snp	A/G	0.000512837	0.0160049	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612282	AAGATTGGTGAGACC[A/G]CACGGCCATTTCTCC	124930
rs371378084	snp	G/T			intron-variant	ANKRD13B	GRCh38.p7	17:29597273	CACATGGGTGTGAGG[G/T]GTGTTCCTGTGCAAA	124930
rs371389990	snp	A/G	0.00186422	0.0304735	missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29613497	TGGAACTGTCGGCGC[A/G]GGAGCAGGAGGAGAG	124930
rs371420286	snp	C/T	0.000437904	0.0147905	intron-variant	ANKRD13B	GRCh38.p7	17:29608305	GCGCTTGCTCCCCTG[C/T]CTGGAATGTGTTCTC	124930
rs371478891	snp	C/G/T	0.000283851	0.0119101	intron-variant	ANKRD13B	GRCh38.p7	17:29609059	CAGGCCACCCCTGAT[C/G/T]CCCCTGTGCTGTTCC	124930
rs371863320	snp	A/C/G	0.000135656	0.00823476	intron-variant	ANKRD13B	GRCh38.p7	17:29609323	CAGCCCGGTGGGGTG[A/C/G]CTGCCTCACCTGGAC	124930
rs371896718	snp	C/G			utr-variant-3-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29613803	GGCACGGCCTGGTCC[C/G]CCTGCTTTGCTGTAT	124930
rs371910809	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29596436	ATGCCAGTTCCCCCT[C/T]GCCTGGCATGGCCAG	124930
rs372020367	snp	A/G			intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29599026	GGGCTTCTGTTCGAG[A/G]TGCAGGAGGTGCTCA	124930
rs372062091	snp	C/G	1.69006e-05	0.00290689	intron-variant	ANKRD13B	GRCh38.p7	17:29609339	CTGCCTCACCTGGAC[C/G]ACTCTGCTTCCCCAG	124930
rs372116363	snp	C/T	0.000177436	0.00941735	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612827	CCAGGTGCGTCTCCG[C/T]GGGCGCGCGGGGCCA	124930
rs372192642	snp	C/T	1.67649e-05	0.0028952	synonymous-codon, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29609096	GGCAGACACAAGCGC[C/T]GTGGTCATGGAGATT	124930
rs372218696	snp	A/G	5.42304e-05	0.00520694	intron-variant	ANKRD13B	GRCh38.p7	17:29610810	GTGTTGCAGGACTGC[A/G]GGAACCAGCTCCCAC	124930
rs372428129	snp	A/G	0.000351938	0.0132607	synonymous-codon, upstream-variant-2KB, intron-variant, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29593687	GCTGCACTACCTCGT[A/G]TGGCACAACCGCCAC	124930
rs372467290	snp	C/G	0.000153988	0.00877328	missense, intron-variant, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29611888	CAGACCCTGATCACT[C/G]AGACTCTGAGCCAAG	124930
rs372550699	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29604547	TTTTTCTTTTCTTTT[C/T]TTTTTTTTTTTTGAG	124930
rs372695970	snp	C/T	0.000125611	0.007924	intron-variant	ANKRD13B	GRCh38.p7	17:29607910	CCCCAGCCCCACAGC[C/T]GGGGCCTCCCCAGCA	124930
rs372774044	snp	C/G	0.000166928	0.00913434	intron-variant	ANKRD13B	GRCh38.p7	17:29609051	GGCAGCCCCAGGCCA[C/G]CCCTGATCCCCCTGT	124930
rs372774750	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29606594	ACAAACAAAACTTAC[A/G]TTTAACAAACATGCT	124930
rs373028767	snp	G/T			intron-variant	ANKRD13B	GRCh38.p7	17:29611306	CGTTTTACTGTCCAG[G/T]GTCACCGAGCTGGAG	124930
rs373085942	snp	A/G			utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant	CORO6, ANKRD13B	GRCh38.p7	17:29615115	GATTTCTTCGCGGGG[A/G]CTGCCGCGAGGAAGC	124930
rs373104400	snp	C/T	3.80539e-05	0.00436182	intron-variant	ANKRD13B	GRCh38.p7	17:29610636	CTTAGGGGTAAGACA[C/T]AGGGTAAGACCAGAA	124930
rs373460828	snp	A/C			intron-variant	ANKRD13B	GRCh38.p7	17:29604349	AGTAGCTGAGGCTAC[A/C]GGCACATGCTACCAT	124930
rs373493420	snp	A/G	1.8334e-05	0.00302765	intron-variant	ANKRD13B	GRCh38.p7	17:29607716	CGTGACTGGGGCTTT[A/G]TCTTCCACTCCTCCT	124930
rs373543908	snp	A/G	3.46057e-05	0.00415952	missense, utr-variant-5-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29608087	CTGGCGGGCATCCCC[A/G]TGCTCCTGGAGAAGC	124930
rs373758478	snp	A/C	0.000798403	0.0199641	intron-variant	ANKRD13B	GRCh38.p7	17:29607077	ACAAAAAAAAACCCC[A/C]AAAAAAGCTTTTATC	124930
rs374046551	snp	A/C	1.77002e-05	0.00297486	intron-variant	ANKRD13B	GRCh38.p7	17:29609448	GCTCCCAGCTGCCAG[A/C]CCAGCTGCACTCTTG	124930
rs374118186	snp	C/T	0.000437904	0.0147905	intron-variant	ANKRD13B	GRCh38.p7	17:29610821	CTGCGGGAACCAGCT[C/T]CCACTTCAGTGCTTC	124930
rs374175298	snp	C/T	0.00159617	0.0282053	intron-variant	ANKRD13B	GRCh38.p7	17:29599630	TTATGGGGGCAGGTG[C/T]AGCTGTCCAGGAATG	124930
rs374207268	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29602457	ATACAAATTTGAGAT[A/G]TTGGCAGGGTGGCAG	124930
rs374216804	snp	C/G/T	3.85611e-05	0.00439082	missense, stop-gained, nc-transcript-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612813	GGCAGTGAGTATGAC[C/G/T]AGGTGCGTCTCCGCG	124930
rs374236380	snp	A/G	3.32967e-05	0.0040801	intron-variant	ANKRD13B	GRCh38.p7	17:29609032	CAGGGTGGGGACGAT[A/G]GGAGGCAGCCCCAGG	124930
rs374533644	in-del	-/C			intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29598499	CCCCTCCCCTTCTCC[-/C]TCCCTCCCTCCCTTC	124930
rs374594772	snp	C/T	0.00108458	0.0232621	intron-variant	ANKRD13B	GRCh38.p7	17:29609058	CCAGGCCACCCCTGA[C/T]CCCCCTGTGCTGTTC	124930
rs374598375	snp	C/T	0.000153988	0.00877328	intron-variant	ANKRD13B	GRCh38.p7	17:29608847	CAACCTCCGCTTCCA[C/T]CAGTGCCCCTGGTGT	124930
rs374614115	snp	A/G/T	0.0024183	0.0346892	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612844	GGCGCGCGGGGCCAC[A/G/T]GGACTCCGCGCCGCC	124930
rs374719276	snp	C/T			intron-variant, utr-variant-5-prime	ANKRD13B	GRCh38.p7	17:29594291	TGGAGAAAGACCCTC[C/T]TGGGAGGCCCCAAGG	124930
rs374732691	snp	A/G	1.77021e-05	0.00297502	intron-variant	ANKRD13B	GRCh38.p7	17:29609451	CCCAGCTGCCAGCCC[A/G]GCTGCACTCTTGCCT	124930
rs374807459	snp	C/G/T	0.000301841	0.0122813	synonymous-codon, missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29609111	CGTGGTCATGGAGAT[C/G/T]GACCACGACCGCCGG	124930
rs374816066	snp	C/T	3.3134e-05	0.00407012	missense, synonymous-codon, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29611978	CGTGATATGGGCCGC[C/T]CCATGGAACTGACCA	124930
rs374823174	snp	C/T	5.10104e-05	0.00505001	intron-variant	ANKRD13B	GRCh38.p7	17:29609313	ACCCTTGAGCCAGCC[C/T]GGTGGGGTGCCTGCC	124930
rs374863654	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29603303	CTGGAGTGCAGTGGC[A/G]TGATCATAGCTCACT	124930
rs374863665	snp	A/G			intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29598097	GCTGCCGGGCTCAGG[A/G]CCCCACCCAGGTTGC	124930
rs374976780	snp	C/G	0.000798403	0.0199641	intron-variant	ANKRD13B	GRCh38.p7	17:29600002	CTGCCTCAGCCTCCC[C/G]AGTAGCTGTGACTAC	124930
rs375133123	snp	C/T	0.000664452	0.0182149	intron-variant	ANKRD13B	GRCh38.p7	17:29610672	TATGAGCCCTTTCTT[C/T]ATCTGTCCCCAGGTG	124930
rs375318309	snp	C/G	3.46476e-05	0.00416204	intron-variant	ANKRD13B	GRCh38.p7	17:29607946	GACCTATGGTTGGCT[C/G]AAGGGTCCTGCCCTG	124930
rs375363344	in-del	-/A/AA	0.486266	0.0817214	intron-variant	ANKRD13B	GRCh38.p7	17:29602394	GTGAGATTCCATCTC[-/A/AA]AAAAAAAAAAAAAAA	124930
rs375412050	snp	C/G			upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29593058	CCACCCCCAGTTTCA[C/G]GAGGCGGACTACAAA	124930
rs375444481	snp	A/G	0.000165185	0.00908655	intron-variant	ANKRD13B	GRCh38.p7	17:29611666	TGTGCAGGGGTACCC[A/G]TAAGTGGAGGGATGT	124930
rs375446982	snp	C/G/T	0.000354475	0.0133086	intron-variant	ANKRD13B	GRCh38.p7	17:29609278	TCTCCTTTGAGAGGT[C/G/T]GGTGGACATGGCCTT	124930
rs375508741	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29610178	GCCTGGGCAACAGAG[C/T]GAGACTCCATCTAAA	124930
rs375514948	snp	C/T	4.96093e-05	0.00498018	intron-variant	ANKRD13B	GRCh38.p7	17:29611564	GTGTCCTCTGAGATG[C/T]CACATTTCTTGTAGG	124930
rs375621568	snp	C/T	0.000153988	0.00877327	intron-variant	ANKRD13B	GRCh38.p7	17:29607730	TATCTTCCACTCCTC[C/T]TCCTCCTCCAGGTGG	124930
rs375658354	snp	A/G	0.000203562	0.0100866	intron-variant	ANKRD13B	GRCh38.p7	17:29607699	CGGAGGGCTGCCTCC[A/G]ACGTGACTGGGGCTT	124930
rs375780472	snp	C/T	0.00119737	0.0244387	intron-variant	ANKRD13B	GRCh38.p7	17:29597293	TCCTGTGCAAATACG[C/T]ACACACACGTTACAC	124930
rs375840069	snp	A/G	0.00199481	0.0315187	intron-variant	ANKRD13B	GRCh38.p7	17:29599963	CTCACTGCAAGCTCC[A/G]CCTCCCGGGTTCACA	124930
rs376027733	snp	A/C	1.65732e-05	0.00287859	missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29608884	TCTGCCCTAGTGACA[A/C]CTACAAAGTGTGGAA	124930
rs376039079	snp	C/T	0.00186354	0.030468	intron-variant	ANKRD13B	GRCh38.p7	17:29610634	CCCTTAGGGGTAAGA[C/T]ACAGGGTAAGACCAG	124930
rs376461322	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29606981	CTTGAACCTGGGAGA[C/T]GGAGGTTACAGCGAG	124930
rs376484013	snp	C/T	8.27219e-05	0.00643072	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612281	TAAGATTGGTGAGAC[C/T]GCACGGCCATTTCTC	124930
rs376492662	snp	A/C	0.00438332	0.0466095	intron-variant	ANKRD13B	GRCh38.p7	17:29604830	TTACAGGCATGAGCC[A/C]CTGCACCCGGCCTGA	124930
rs376640359	snp	C/T	1.6483e-05	0.00287076	synonymous-codon, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29612200	TGACCTCATGGCCGT[C/T]AGCAATGCGCTTTTT	124930
rs376855975	snp	C/G/T			intron-variant	ANKRD13B	GRCh38.p7	17:29607648	CAGCCCCAGCAGGGG[C/G/T]TGGGGGTTGCTGCCT	124930
rs376863719	snp	C/T	1.65712e-05	0.00287843	intron-variant	ANKRD13B	GRCh38.p7	17:29608180	GACTTAGCCTCTCTC[C/T]CCTTCGTCCTCCAGG	124930
rs376939849	snp	A/G			intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29597601	ATGGGAAACCTTTTC[A/G]TTCCAGCAATTAAAT	124930
rs376969268	snp	C/G			intron-variant	ANKRD13B	GRCh38.p7	17:29603663	ATCTGCTGTTATTTC[C/G]ATTCAGTGAATTTTT	124930
rs376995271	snp	A/G	5.04299e-05	0.0050212	synonymous-codon, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29609204	TCAGCCCACTGAGGA[A/G]CAGGTGCTGAGCCGG	124930
rs377075825	snp	A/G	6.69848e-05	0.00578688	missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29609125	TTGACCACGACCGCC[A/G]GGTGGTGTACACAGA	124930
rs377281777	snp	G/T	0.000153988	0.00877328	missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29609163	GCACTGGCTGGGCAG[G/T]ACCGGGAGCTGCTGC	124930
rs377406629	snp	A/C/T	3.71666e-05	0.00431071	intron-variant	ANKRD13B	GRCh38.p7	17:29610653	GGGTAAGACCAGAAC[A/C/T]GCTTATGAGCCCTTT	124930
rs377553091	snp	C/T			upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29593222	GGGACCCGGGGGCTG[C/T]GGGCGCGCGTCCCTG	124930
rs377560958	snp	A/G	0.00636936	0.0560724	intron-variant	ANKRD13B	GRCh38.p7	17:29602834	GGAAAAATTTTGGAC[A/G]TTCTTTCTTTCTTTT	124930
rs377675322	snp	C/T	1.7203e-05	0.00293278	intron-variant	ANKRD13B	GRCh38.p7	17:29607973	CCTGTGACCTTGCCT[C/T]GCCCTCCCCCAGTGC	124930
rs386385871	in-del	-/TT			intron-variant	ANKRD13B	GRCh38.p7	17:29599866	TAGCATCTAATTTGT[-/TT]TTTTTTTTTTTTTTT	124930
rs397741966	in-del	-/A	0	0	intron-variant	ANKRD13B	GRCh38.p7	17:29602412	AAAAAAAAAAAAAAA[-/A]TTTATTCTGTCACAG	124930
rs527486359	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29591695	TACAGTGGAATCACA[C/T]ACAAGGTTCGAAAAA	124930
rs527683671	snp	G/T	0.00358779	0.0422022	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29594029	TGTGTCGGTGTTCCA[G/T]GTGGTGGGAGAGTCC	124930
rs527684286	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29608334	TCATAGTTCTTCCGG[C/T]GGTTCCCTCTATGCC	124930
rs527694500	snp	A/G	0.000798403	0.0199641	intron-variant	ANKRD13B	GRCh38.p7	17:29594670	GGGTGGGCTGCAAGA[A/G]CCAGAGCTGGGCCCG	124930
rs528011050	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29601052	ACCTCAGCCTCCCAG[C/T]AGCTGGGACGATAGG	124930
rs528064854	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29605441	ACACACACATACACA[C/T]ACACATATATATATA	124930
rs528082605	snp	A/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29596929	ACATGGAGGGAGAAG[A/T]CCAGGGTGCGGTCCC	124930
rs528224858	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29610042	CTAACAATACAAAAA[A/G]TTAGCCGGGTGTGGT	124930
rs528394200	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29608584	ATTTGTTGAAAGAAT[A/G]GATGAAAGAGTGAGT	124930
rs528413477	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29604651	GGTTCAAGTGATTCT[C/T]GTGCCTCAGCCTCCT	124930
rs528456853	snp	A/C	0.00128415	0.0253067	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612647	CCCAGCCCCCGCGCC[A/C]CCAGCCTCCTGCCGC	124930
rs528508387	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29613671	GCGCGCCTGCAGAGC[A/G]GCGGCTGGAGACTGG	124930
rs529080158	snp	C/G			intron-variant	ANKRD13B	GRCh38.p7	17:29609320	AGCCAGCCCGGTGGG[C/G]TGCCTGCCTCACCTG	124930
rs529324235	snp	C/G			intron-variant	ANKRD13B	GRCh38.p7	17:29595158	GAGAAGCCTGTTAAA[C/G]AGAGTGGGTCACAGT	124930
rs529446074	snp	G/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29595712	TGTCTCCTTGAAATG[G/T]ACACTGCCTGTCCTG	124930
rs529477394	snp	C/T	0.00199481	0.0315187	intron-variant	ANKRD13B	GRCh38.p7	17:29602770	GATGTGGACATGTCT[C/T]AGGAGGGGCACCATT	124930
rs529756909	snp	A/C			intron-variant	ANKRD13B	GRCh38.p7	17:29604315	CTGGGCTTAAGGGAT[A/C]CTCCTGCCTCAGTCA	124930
rs529903620	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29599215	GGGGAAGGCCATTGG[C/T]GAAGGGTGGAGCAAA	124930
rs529945472	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29605935	TTTTTTTTTTGAGAC[A/G]GAGTTTTGCTCTTGT	124930
rs530110300	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29600056	TAATTTTTTGTATTT[C/T]TAGTAGAGACGGGGT	124930
rs530122819	snp	A/T	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29592833	TGGGACCCAAGCTCA[A/T]TTCTGAAGACCACAC	124930
rs530185173	snp	G/T	0.00716266	0.059414	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29593800	GTCCGGCCTGGGGAG[G/T]GGGTGCGGCGCGGGC	124930
rs530267540	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29614164	CCAGCCCCCACACCC[A/G]TCCTGGGTCTCAGGG	124930
rs530352798	snp	A/G	0.000798403	0.0199641	intron-variant	ANKRD13B	GRCh38.p7	17:29607442	CACTGGGCCCTGGAG[A/G]AGAGGACCCAGCCAG	124930
rs530416643	snp	C/G	0.000798403	0.0199641	intron-variant	ANKRD13B	GRCh38.p7	17:29610408	CTCCTTATAGAGATT[C/G]TAAGTCTCAGGAGGG	124930
rs530509162	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29603547	ACTATAGAAGCCCAG[C/T]CAACTTTATTTTTCA	124930
rs530524732	snp	A/C	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29604617	TGCAGTCTTGGCTCA[A/C]TGCAACCTCCGCCTC	124930
rs530524737	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29596340	GCACCCAGCAGTGCT[A/G]TGATGCCAGCCCGGT	124930
rs530587216	snp	A/G	0.00119737	0.0244387	intron-variant	ANKRD13B	GRCh38.p7	17:29596826	TAAGCTAGGAAGCTC[A/G]GGAGAGGGAGCCACA	124930
rs530844670	snp	A/G			intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29597606	AAACCTTTTCATTCC[A/G]GCAATTAAATAGCTA	124930
rs530952021	snp	A/G	0.000798403	0.0199641	intron-variant	ANKRD13B	GRCh38.p7	17:29611273	ACATGCACACCCCAC[A/G]GTGCCTGCCGGGGCA	124930
rs531098491	snp	C/G			upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29592748	CCTTGGTACTGATGC[C/G]CCACACCTTTCTCAG	124930
rs531161351	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29592653	TGACATGTGTGGAAG[A/G]TGGAGTTTAATTTTC	124930
rs531250057	snp	C/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29597622	GCAATTAAATAGCTA[C/G]AGGCCTCTGCTGAGG	124930
rs531594103	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29602267	GGGCGTGGTGGTGGG[C/T]GCCTGTAATCCCAGC	124930
rs531727272	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29595622	GGGCTGCTCATGTGT[C/T]TCTCTCTCCCACCCC	124930
rs531748889	snp	A/G	0.000798403	0.0199641	intron-variant	ANKRD13B	GRCh38.p7	17:29608640	TAGGGACTTAGTGGT[A/G]ACAGAAACATGCCCG	124930
rs531780262	snp	A/G	0.000798403	0.0199641	intron-variant	ANKRD13B	GRCh38.p7	17:29601145	CCCACGCTGGTTTCA[A/G]ACTCCTGGGCTCAAG	124930
rs531882480	snp	A/G	0.000798403	0.0199641	intron-variant	ANKRD13B	GRCh38.p7	17:29605952	AGTTTTGCTCTTGTC[A/G]CCCAGGCTGGAGTGC	124930
rs531945397	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29594786	AGTTGCCCGCTGTGG[A/G]AATTTACCTTCTGAG	124930
rs532010487	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29598287	AAAAATTATATAAAT[A/G]ATCTTAAATTATTTA	124930
rs532133818	snp	A/C	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29611231	AAATCATGCCTATGG[A/C]AGTGCCTGAAGCAAA	124930
rs532195209	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29605628	CAGGCCATCATACCC[A/G]GCTAATTCTTTTGTA	124930
rs532453265	snp	A/C			intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612876	CGGCTAACGCCCACG[A/C]CTCCCCGCAGGTCAC	124930
rs532469124	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29597678	GATTAATGAATTCTC[A/C]TACCTGGGCCCAGGG	124930
rs532504350	snp	A/G			intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29613036	CAGGACACAGCCGGA[A/G]AACCCGCGGGGCCCT	124930
rs532504987	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29606824	GAGCCCGAGCCAGGT[A/G]GATCACCTGAGGTCA	124930
rs532557215	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29604707	TCACCAAGCCCGGCT[A/G]ATTTTTTGTATTTTT	124930
rs532572394	snp	C/T	0.000798403	0.0199641	intron-variant	ANKRD13B	GRCh38.p7	17:29607329	TTCCTGAAGGTGGCC[C/T]GGGACCCTTAGGGTA	124930
rs532671591	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29591793	CCCTCCCCTGCACTG[A/G]CTGCAGCCACGACAC	124930
rs532822682	snp	A/C	4.23343e-05	0.00460058	missense, downstream-variant-500B, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29612679	GCTGCGAGATCTCCC[A/C]AGCGTTGTTCGAGGC	124930
rs532922766	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29595761	TATAGGGCACTGGTG[A/G]AGGTTAACCCTTGTT	124930
rs533096345	snp	G/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29603363	CCTCCTGCCTCAGCT[G/T]CAGAGGAGCTGGGAC	124930
rs533394178	snp	A/C			intron-variant	ANKRD13B	GRCh38.p7	17:29601931	ACCTCATTTCTTTGA[A/C]TGCTTTTAGGATTTT	124930
rs533516579	snp	A/G	0.000307267	0.0123911	synonymous-codon, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29613489	GCTGGCGATGGAACT[A/G]TCGGCGCAGGAGCAG	124930
rs533570455	snp	A/G	0.00119737	0.0244387	intron-variant	ANKRD13B	GRCh38.p7	17:29596305	ATGGGCAGATAGGAG[A/G]TGCCTGGTGAAGGGA	124930
rs533617237	snp	G/T			utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant	CORO6, ANKRD13B	GRCh38.p7	17:29615090	TAACTCCTCATGCCA[G/T]TTCTCTCGAGATTTC	124930
rs533627149	snp	C/T	0.000798403	0.0199641	downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	CORO6, ANKRD13B	GRCh38.p7	17:29614284	TGTCCAACGTAGCCC[C/T]CTGGCCTGTGCAAGC	124930
rs533868233	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29606440	GTGCTCGCCTGTAAT[C/T]CCAGCTACTCAGAAG	124930
rs534187378	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29606278	ATACTTATGCTTAAG[A/G]CCGGGCGTGGTGGCT	124930
rs534531653	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29603646	AAATTGTGCAGTGTC[C/T]AATCTGCTGTTATTT	124930
rs534544901	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29592911	TTCCCCAGCAAAAGG[C/T]AAAATGCCAGCGGGG	124930
rs534601119	in-del	-/T			intron-variant	ANKRD13B	GRCh38.p7	17:29601225	CCAGCCTGACATTCT[-/T]TTTTTTTTTTTTTTG	124930
rs534836343	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29595996	TAACATCATGAGAAA[A/G]GCACTGTGGAACCCT	124930
rs535199996	snp	C/G	0.000798403	0.0199641	intron-variant, utr-variant-5-prime	ANKRD13B	GRCh38.p7	17:29594343	GCGCTCTCCTGCCCT[C/G]TGGTGCTGGGGCCTG	124930
rs535321324	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29610940	GGGTAGTGGCTGCCT[A/G]GAGTACTAAGAAGTT	124930
rs535378889	snp	A/C	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29604956	TTAAATATGCATCTC[A/C]ACTCTAGGAGGCTGG	124930
rs535380654	snp	C/T	8.61764e-05	0.0065636	intron-variant	ANKRD13B	GRCh38.p7	17:29607970	TGCCCTGTGACCTTG[C/T]CTCGCCCTCCCCCAG	124930
rs535390004	snp	C/T	0.000798403	0.0199641	intron-variant	ANKRD13B	GRCh38.p7	17:29611400	CACAGAGGCCCTGGC[C/T]CCTGGTCCTTGAAGC	124930
rs535422262	snp	C/G	0.00279162	0.0372561	intron-variant	ANKRD13B	GRCh38.p7	17:29607672	GCTGCCTGCTCCAGG[C/G]CTGTCTGGCTCCGGA	124930
rs535448507	snp	A/C	0.00119737	0.0244387	intron-variant	ANKRD13B	GRCh38.p7	17:29601277	CCCAGGCTGGAGTGC[A/C]GTGGTGCGATCTCTG	124930
rs535722916	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant	CORO6, ANKRD13B	GRCh38.p7	17:29615255	CAGAACTGGGGTGAC[A/G]CCCATCTGGTTTACC	124930
rs535994428	snp	C/G	1.74558e-05	0.00295425	intron-variant	ANKRD13B	GRCh38.p7	17:29609436	GGTGAGGCTGCAGCT[C/G]CCAGCTGCCAGCCCA	124930
rs536002337	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29613282	CCGCCCTGGAGCCTC[C/T]ACGCCGTGTCCCGGC	124930
rs536386603	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29606005	GCAACCTCCGCCTCC[C/T]GGGTTCAAGCGGTTC	124930
rs536510237	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29602833	TGGAAAAATTTTGGA[C/T]GTTCTTTCTTTCTTT	124930
rs536635410	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29592200	CTTAGCTCACCCCAG[G/T]AGGTAGTATCTAGAT	124930
rs536762266	in-del	-/TT			intron-variant, utr-variant-5-prime	ANKRD13B	GRCh38.p7	17:29594309	GAGGCCCCAAGGGCC[-/TT]TTGTCCAGGTGCTGA	124930
rs536920398	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29595839	AAAAAGAGGAATGCC[A/G]CTCCGTGTAGGTGGG	124930
rs536972810	snp	G/T	0.00119737	0.0244387	intron-variant	ANKRD13B	GRCh38.p7	17:29599567	CAGTTTTAAAGTTGG[G/T]TTTTTTTTCCACCTG	124930
rs537000008	snp	C/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29610816	CAGGACTGCGGGAAC[C/G]AGCTCCCACTTCAGT	124930
rs537000406	snp	C/T	0.000798403	0.0199641	intron-variant	ANKRD13B	GRCh38.p7	17:29604020	TGCTGGGATTACAGG[C/T]TCACGTGAGCCACCG	124930
rs537035133	snp	C/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29595880	AGCTGTCTCCCCTCT[C/G]GAGGACTGGCCCAGA	124930
rs537060880	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29596608	CAGAACCCTGAAGTG[A/G]GCAGATTGTGGTCCC	124930
rs537262601	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29602138	TGGTGGCTCACGCCT[A/G]TAATCCCAGCATTTT	124930
rs537373304	snp	A/G	0.000798403	0.0199641	intron-variant	ANKRD13B	GRCh38.p7	17:29595191	CCCCAGGAAACAGAT[A/G]AACAAACAGGGCATC	124930
rs537404083	snp	A/G	0.00199481	0.0315187	intron-variant	ANKRD13B	GRCh38.p7	17:29607045	ACAGAGTGAGACTCC[A/G]TCCCCCCAAAAAAAA	124930
rs537466481	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29607630	GAGGTTGGTGAGGCA[A/G]AGCAGCCCCAGCAGG	124930
rs537579908	snp	C/T	0.000798403	0.0199641	intron-variant	ANKRD13B	GRCh38.p7	17:29600116	CTCCTGACCTCGTGA[C/T]CCGCCCACCTCGGCC	124930
rs537793790	snp	C/T	0.00159617	0.0282053	downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	CORO6, ANKRD13B	GRCh38.p7	17:29614443	TGCTGCTAGCCTCTG[C/T]GGTTGTACATCCCAC	124930
rs537912883	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29606911	AAAAATTAGCCAGAC[A/G]TGTTGGCGAATGTCT	124930
rs538046813	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29593004	CCGCCCACTCTCCCA[A/C]GAGATCCGGGGACAG	124930
rs538454168	snp	A/C	0.000798403	0.0199641	intron-variant, utr-variant-5-prime	ANKRD13B	GRCh38.p7	17:29594241	GGCAGATCCTTGGAT[A/C]TCTCAGAGCCCAGCC	124930
rs538781818	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29610993	GTGGAGAGCCATGCT[A/G]CAAGTGATTACTAAT	124930
rs538782129	snp	C/G			intron-variant	ANKRD13B	GRCh38.p7	17:29602947	ACCTCCCCTTCCCGG[C/G]TTCAAGCGATTCTCC	124930
rs538817182	snp	C/G			intron-variant	ANKRD13B	GRCh38.p7	17:29606462	ACTCAGAAGGCTGAG[C/G]CACAAGAATCGCTTG	124930
rs539020656	snp	A/G	0.00159617	0.0282053	intron-variant, utr-variant-5-prime	ANKRD13B	GRCh38.p7	17:29594465	AGTAAGGCCACGTGG[A/G]TCACCAGCTTTGGGC	124930
rs539088465	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29605266	AATTACAGTCTGGAA[C/T]GTTCCTCCAGGCAGA	124930
rs539089616	in-del	-/T			intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29598557	TTCTTCTTTTTTTTC[-/T]TTTTTTCATGAGACA	124930
rs539205155	snp	C/T	0.000798403	0.0199641	intron-variant	ANKRD13B	GRCh38.p7	17:29611469	TTGGGTGAGCAGGCC[C/T]CACCCCAGGAACCGG	124930
rs539322901	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29605951	GAGTTTTGCTCTTGT[C/T]GCCCAGGCTGGAGTG	124930
rs539375893	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29602085	CAACAAATTACTACA[A/G]ACTAGGTGGGTTAAA	124930
rs539385440	snp	C/T	0.000798403	0.0199641	intron-variant	ANKRD13B	GRCh38.p7	17:29606296	GGGCGTGGTGGCTCA[C/T]GCCTGTAATCCCAAC	124930
rs539396610	snp	A/T	0.00119737	0.0244387	intron-variant	ANKRD13B	GRCh38.p7	17:29601438	TGTTGGCCAGGCTGG[A/T]CTCAAACTCCTGACC	124930
rs539438467	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29595039	CTGGGTGGCCACTTC[C/T]TGTTACCTGTGCCTA	124930
rs539530876	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29603138	ACAGGCGTGAGCCAC[C/T]GCACCCGGCCTATTT	124930
rs539729660	snp	C/T	5.04868e-05	0.00502403	intron-variant	ANKRD13B	GRCh38.p7	17:29608136	GCCTCTCAGCCTCCA[C/T]GGGAGCCCTTGAGCC	124930
rs539765251	snp	C/T			intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29599266	GGGCCATTGGATTCC[C/T]TGCTACCTACGATGG	124930
rs539788844	snp	A/C	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29608781	CGGATCCCAAACCCC[A/C]TGCCCTGAGCTGGTC	124930
rs540133401	snp	A/G	0.00517822	0.0506191	intron-variant	ANKRD13B	GRCh38.p7	17:29611216	CAGGGGAACAACATG[A/G]AATCATGCCTATGGA	124930
rs540144063	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29611750	GGACCTCCTTTCCAC[A/G]ATGCCCAAGGCCATG	124930
rs540486369	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29600540	AGTCCAGAGCATCTC[A/G]TGCCCAATTTCTACA	124930
rs540526802	snp	C/T	0.000798403	0.0199641	intron-variant	ANKRD13B	GRCh38.p7	17:29605447	ACATACACACACACA[C/T]ATATATATACACACA	124930
rs540610418	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29607374	TGAGCTCCTTGGCCA[A/G]CAGCCTCTTTGCCAC	124930
rs540661688	snp	G/T	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29613677	CTGCAGAGCGGCGGC[G/T]GGAGACTGGAGCCAC	124930
rs540685246	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29599717	GGGCAGGAGACGTCA[C/T]GGAAAGCCAGGCTGT	124930
rs540724570	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant	CORO6, ANKRD13B	GRCh38.p7	17:29614902	ATCGCCAGGTCTCCC[A/G]GGAGCCTGGGGGTAG	124930
rs540736819	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29607219	GAAATTGTATTAATA[C/T]CATGAACTTGTTATT	124930
rs540869939	snp	C/G			intron-variant	ANKRD13B	GRCh38.p7	17:29600581	CCCTGGTGTCCTGTG[C/G]TGAGGAAGGGGGGCA	124930
rs540875927	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29604499	GAGGTGTGAGCCACC[A/G]TGCCTGGCCTTTGAT	124930
rs541409637	snp	A/G	0.000798403	0.0199641	intron-variant	ANKRD13B	GRCh38.p7	17:29596670	CTCCACCGTGGGCTT[A/G]CTTCCTGCTTTCCCT	124930
rs541437935	snp	A/G			upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29592240	GAAGGGGAGTGGACC[A/G]AGAAAGTCGGAAAAA	124930
rs541439316	snp	A/G	0.00199481	0.0315187	upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29593094	TGATGCCGCGGGGCT[A/G]AGCTGACAAGCTCTA	124930
rs541586972	snp	C/G	0.00119737	0.0244387	intron-variant	ANKRD13B	GRCh38.p7	17:29603276	AGACAGGGTCTTGCT[C/G]TGTTGCCCAGGCTGG	124930
rs541612267	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29610247	CCCCTATGTTGCCCA[C/T]GACATGAAAGCAGGA	124930
rs541633044	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29606606	TACGTTTAACAAACA[C/T]GCTTTCTAAGCCAGG	124930
rs541698185	snp	G/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29596266	GCCCCAAATTGCTCT[G/T]CTGGAGGCTGGAAGC	124930
rs541769433	snp	C/G	0	0	intron-variant	ANKRD13B	GRCh38.p7	17:29599916	GAGTCTCGCTCTGTC[C/G]CCCGCGCTAGAGTGC	124930
rs541832417	snp	G/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29600915	TGGGTTTTAAATATT[G/T]TACTGACTTTTTTTT	124930
rs542169693	snp	C/G	8.75128e-05	0.00661428	missense, utr-variant-5-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29607808	ACCACGCTGGGGCAC[C/G]TTGAGTGTGCCCGTG	124930
rs542182466	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29608332	TCTCATAGTTCTTCC[A/G]GCGGTTCCCTCTATG	124930
rs542294101	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29601587	TACAGATTCAAGTTT[C/T]TATCTGGGATCATTT	124930
rs542335406	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29605200	TGAATCCTGTCTCCA[C/T]CTTCTCAACTCAGGA	124930
rs542574065	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29604627	GCTCACTGCAACCTC[C/T]GCCTCCTGGGTTCAA	124930
rs542765427	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29613647	CAGGAGCCAGACAAA[A/C]CCCGGCCTGCGCGCC	124930
rs542774337	snp	C/G			intron-variant	ANKRD13B	GRCh38.p7	17:29605728	CCAACCTTTGCCTCC[C/G]AAATTGCTGGGATTA	124930
rs543202795	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29593777	GGACCCCGCGGCCGG[G/T]CACGCCCGTCCGGCC	124930
rs543364438	snp	A/G	0.000798403	0.0199641	intron-variant	ANKRD13B	GRCh38.p7	17:29596171	CCGCAGAGGCCCTCC[A/G]TGGGCAGGCTTGGCA	124930
rs543659998	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	ANKRD13B	GRCh38.p7	17:29594505	GTCTCCAGAAAACAG[A/G]GGAAGGGGGGATGTC	124930
rs543736228	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29609622	GCACGTGCACACGCA[C/T]ACACACACACACATT	124930
rs543745173	snp	C/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29603210	TTTGGGATTCCAATA[C/G]ATATATGTTACAATG	124930
rs543785435	snp	C/T			upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29592660	TGTGGAAGATGGAGT[C/T]TAATTTTCTAACAGG	124930
rs544143930	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29598319	AATGTTTCATTTTTG[A/G]CAATGGAGTTCATGG	124930
rs544324211	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29592529	GGGTGGAGGAACGGA[A/G]CTGCCACCTGCTGCT	124930
rs544583208	snp	C/T	0.00159617	0.0282053	intron-variant	ANKRD13B	GRCh38.p7	17:29607343	CTGGGACCCTTAGGG[C/T]AGGTCTGGTCCCAGG	124930
rs544685822	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29601485	CCTCGGCCTCCCAAA[A/G]TGCTGGGATTACAGG	124930
rs544693930	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29607715	ACGTGACTGGGGCTT[C/T]ATCTTCCACTCCTCC	124930
rs544756960	snp	C/G	0.000798403	0.0199641	intron-variant	ANKRD13B	GRCh38.p7	17:29600775	TGTGGACGTTTCCCT[C/G]TGTGGCTGCTTTAGT	124930
rs544970178	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29600098	AGCCAGGATGGTCTC[A/G]ATCTCCTGACCTCGT	124930
rs544986780	snp	A/G	0	0	intron-variant	ANKRD13B	GRCh38.p7	17:29609708	ACGCATGTTTATTGA[A/G]TCCTTTCCTTGGCAT	124930
rs545093898	snp	A/G	0.00318978	0.0398085	intron-variant	ANKRD13B	GRCh38.p7	17:29599900	TTTTTTTTTTGATAC[A/G]GAGTCTCGCTCTGTC	124930
rs545106014	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29610324	CTCCCCTGCTTCTGT[A/G]GTCTGGGAAGGCCTC	124930
rs545165468	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29604395	TGTATTTTTTGTAGA[C/T]ATGGGGTTTTGGTAT	124930
rs545288526	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29597410	CGAGTGTGTATCTGT[A/G]TGGTACCAGTGTGTA	124930
rs545538461	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29596819	CAGCTGGTAAGCTAG[A/G]AAGCTCGGGAGAGGG	124930
rs545651395	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29599946	CAGTGGCGCAATCTC[A/G]GCTCACTGCAAGCTC	124930
rs545938797	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29604789	CTCAGGTGATCTGCC[C/T]GCCTCCGCCTCCCAA	124930
rs546047310	snp	C/G			intron-variant	ANKRD13B	GRCh38.p7	17:29596861	CCAGAAACCAAAAAT[C/G]AATGTGTTCTGGGAT	124930
rs546096254	snp	A/G	1.6795e-05	0.0028978	missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29609118	ATGGAGATTGACCAC[A/G]ACCGCCGGGTGGTGT	124930
rs546124464	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29593188	CCGCTCGGGCTGAGG[C/G]CCGGGCTATGCAGCT	124930
rs546421025	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29610550	ATGAATGACCTCATA[C/T]ATTCACTTACCCAAA	124930
rs546545231	snp	A/T	0.00716266	0.059414	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29597647	CTGAGGAGAAGCTGG[A/T]GGCCTCTGCTGAGGA	124930
rs546587309	snp	A/C	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29596986	TGAGGATGCATCCTG[A/C]CTCCCTCCCCTTGAA	124930
rs546757154	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29598723	TGGCTAATTTTTGTA[A/T]TTTTTTTTGTAGAGA	124930
rs546866941	in-del	-/CTTGCCTCA			intron-variant	ANKRD13B	GRCh38.p7	17:29606022	GGTTCAAGCGGTTCT[-/CTTGCCTCA]GCCTCCTGATTAGCT	124930
rs546983198	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29606249	GAAGTCCTAGACTCT[C/T]GAAATATATTTAAAT	124930
rs547078769	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	ANKRD13B	GRCh38.p7	17:29599431	GCCAGTGAGAGATGG[A/G]GGGGCAACAGCTGCA	124930
rs547097879	snp	A/G	0.000798403	0.0199641	intron-variant	ANKRD13B	GRCh38.p7	17:29594885	GGAGGGCAGGCCATC[A/G]GACTGAGCAGGCTGG	124930
rs547101127	snp	A/G			intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29597986	GTCTTATTAGCTGCA[A/G]CGGCTGCGGCTGCAG	124930
rs547111576	snp	G/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29606778	TTTTGTCTGGGCACT[G/T]CGGCTCACACCTGTA	124930
rs547184163	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29602826	TCAAGTTTGGAAAAA[C/T]TTTGGACGTTCTTTC	124930
rs547231661	in-del	-/GGGCTGA	0.00159617	0.0282053	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612342	GATGAGGTCGGGGTG[-/GGGCTGA]GGCTGAGGTGTGAGG	124930
rs547252050	in-del	-/AAAAA			intron-variant	ANKRD13B	GRCh38.p7	17:29606754	AAAAAAAAAAAAAAA[-/AAAAA]AATCTTTTGTCTGGG	124930
rs547323288	snp	A/G	7.89235e-05	0.00628136	missense, downstream-variant-500B, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29612661	CCCCAGCCTCCTGCC[A/G]CGGCTGCGAGATCTC	124930
rs547394705	snp	A/G	5.04944e-05	0.00502441	missense, utr-variant-5-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29608010	AGGCTGTGAGTACCC[A/G]GGACCTGGAGCTGGT	124930
rs547403874	snp	C/G	0.000798403	0.0199641	intron-variant	ANKRD13B	GRCh38.p7	17:29608750	TCTTCAGTTCCCTCC[C/G]CTGTTCCTGGCCACA	124930
rs547462969	snp	A/G	0.000798403	0.0199641	intron-variant	ANKRD13B	GRCh38.p7	17:29602004	GGTGTAGTTTACTTC[A/G]TGTTTGTCTTACTTG	124930
rs547555632	snp	A/G	0.000798403	0.0199641	intron-variant	ANKRD13B	GRCh38.p7	17:29595713	GTCTCCTTGAAATGG[A/G]CACTGCCTGTCCTGG	124930
rs547955396	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29598599	TGTCACCCAGGCTGG[A/G]GTGCAGTAGTGTGAT	124930
rs548008465	snp	A/G	0.000399281	0.0141238	downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	CORO6, ANKRD13B	GRCh38.p7	17:29614566	ACAGACCCCGCCAGG[A/G]GCAGGGGCCCACCGC	124930
rs548305215	snp	C/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29605155	TTCCAGAACTGTGCT[C/G]TGCTGCAACCTTTAA	124930
rs548409211	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant	CORO6, ANKRD13B	GRCh38.p7	17:29615125	CGGGGGCTGCCGCGA[A/G]GAAGCAGCCCTCGCC	124930
rs548533243	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29606918	AGCCAGACGTGTTGG[C/T]GAATGTCTGTAATCC	124930
rs548576945	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29592855	AGACCACACCTCCAC[A/C]CCGTCTCCCAAACGC	124930
rs548689031	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29593910	ATCCCCTCCGGCCGG[A/G]ACGGGCGGGACCACA	124930
rs548861157	snp	A/G	0.000798403	0.0199641	intron-variant	ANKRD13B	GRCh38.p7	17:29607446	GGGCCCTGGAGGAGA[A/G]GACCCAGCCAGGGGC	124930
rs548875085	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29600077	GAGACGGGGTTTCAC[C/T]GTGTTAGCCAGGATG	124930
rs549076794	snp	A/G	0.000798403	0.0199641	intron-variant	ANKRD13B	GRCh38.p7	17:29596862	CAGAAACCAAAAATC[A/G]ATGTGTTCTGGGATG	124930
rs549077150	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29597838	GCTCCTGAGGTGTGG[A/G]GATGGGGAGGAGCAC	124930
rs549198487	snp	A/G	3.37758e-05	0.00410935	synonymous-codon, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29609394	GCGCAGTGAAAAGAC[A/G]GAGATGGTGAATGGG	124930
rs549466427	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29606200	ACAGGCGTGAGCTAC[C/T]GCGCCTGGCCTGTCA	124930
rs549610763	snp	G/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29608651	TGGTGACAGAAACAT[G/T]CCCGTCCCGACCTCA	124930
rs549633287	in-del	-/CGGCAGGG	0.000139655	0.00835512	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29613052	AACCCGCGGGGCCCT[-/CGGCAGGG]ACCCTCCTGGTATCG	124930
rs549661373	in-del	-/GAACCCGCGGGGCCC	0.000192641	0.00981241	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29613036	CAGGACACAGCCGGA[-/GAACCCGCGGGGCCC]TCGGCAGGGACCCTC	124930
rs549831876	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant	CORO6, ANKRD13B	GRCh38.p7	17:29615227	TGCAGCAAACGGGTT[G/T]TGTATGTGTCTGCAG	124930
rs549836605	snp	C/T	1.77225e-05	0.00297673	intron-variant	ANKRD13B	GRCh38.p7	17:29607929	GCCTCCCCAGCATCA[C/T]AGACCTATGGTTGGC	124930
rs549927396	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-5-prime	ANKRD13B	GRCh38.p7	17:29594282	AACAGGGAGTGGAGA[A/G]AGACCCTCTTGGGAG	124930
rs550039193	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29594842	TCAGTCTGAGGAGCT[A/G]TGCAATCGCCAAGGG	124930
rs550090262	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29607285	AAACCTCACTCAGTG[A/G]TAATGTCAGTGATCT	124930
rs550487733	snp	A/C			intron-variant	ANKRD13B	GRCh38.p7	17:29602365	ACGCCACTGCACTCC[A/C]GCCTGGGCGACAGAG	124930
rs550773264	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29591993	AAGAAACCTGAGAGA[C/G]TTTGCAAGCTTTTGC	124930
rs550957928	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29599514	AGTTTTTCTGATGGG[C/T]TAGATGTGGAGGGTG	124930
rs551070741	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29600001	CCTGCCTCAGCCTCC[C/T]GAGTAGCTGTGACTA	124930
rs551091680	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29592757	TGATGCCCCACACCT[G/T]TCTCAGGAGTTCCCA	124930
rs551154880	in-del	-/G	0.00438332	0.0466095	upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29592588	CTGGGGACAGTGTGC[-/G]GGGGGGAAAGGGACC	124930
rs551209822	snp	A/G			upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29593102	CGGGGCTGAGCTGAC[A/G]AGCTCTACCCGGGGC	124930
rs551257285	in-del	-/GAG			intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29597658	CTGGAGGCCTCTGCT[-/GAG]GAGATTAATGAATTC	124930
rs551283646	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29606325	ACACTTTGGGAGGCC[A/G]AGGCAGGCGAATCAC	124930
rs551299735	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29606836	GGTGGATCACCTGAG[A/G]TCAGGAGTTCAAGAC	124930
rs551363586	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29602856	CTTTCTTTTATTATT[C/T]ATTTACTTATTTTGA	124930
rs551436102	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29595837	CCAAAAAGAGGAATG[C/T]CACTCCGTGTAGGTG	124930
rs551462827	snp	A/C	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29604700	GCACCCATCACCAAG[A/C]CCGGCTAATTTTTTG	124930
rs551483176	snp	A/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29603397	AGCTGCTTGCCACCA[A/T]GCCCAGCTAATGTAA	124930
rs551693449	snp	C/T	1.66302e-05	0.00288355	synonymous-codon, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29608856	CTTCCACCAGTGCCC[C/T]TGGTGTCCAAGATCT	124930
rs551781962	snp	A/C			intron-variant	ANKRD13B	GRCh38.p7	17:29602323	TGGCGTGAACCGGGG[A/C]AGCGGAGCTTACAGT	124930
rs551855031	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29611253	TGAAGCAAACACACA[C/T]ACGCACATGCACACC	124930
rs551862016	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29607542	GCCCCTTTCCATCCA[C/T]GTGTCTGTCTTTCCG	124930
rs552096730	snp	C/T			upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29591779	CAACCGCGCCAGCCC[C/T]CTCCCCTGCACTGGC	124930
rs552212579	snp	C/T	0.000798403	0.0199641	intron-variant	ANKRD13B	GRCh38.p7	17:29601087	CACCACCACGCCTGG[C/T]TAATTTTAGTATTTT	124930
rs552319985	snp	A/C	0.00199481	0.0315187	upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29591766	CCTAGATGCCCCTCA[A/C]CCGCGCCAGCCCCCT	124930
rs552321075	snp	C/T	8.78356e-05	0.00662647	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29607846	GGCGCACGGCGCAGA[C/T]GTGGGCAGGGAGAAT	124930
rs552459618	snp	A/G	0.000143688	0.00847488	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29613024	TCTCCCCTAAGCCAG[A/G]ACACAGCCGGAGAAC	124930
rs552461933	snp	A/C	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29600099	GCCAGGATGGTCTCG[A/C]TCTCCTGACCTCGTG	124930
rs552875321	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29594069	AGTTGAGCGGCGACA[C/T]CTCCCGAGTGAGGGT	124930
rs552911222	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29602895	CTCCCTCTGTCGCCC[A/G]AGCTGGAGTGCAGTG	124930
rs552925578	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29595998	ACATCATGAGAAAAG[C/T]ACTGTGGAACCCTGG	124930
rs552978032	in-del	-/T	0.00597247	0.0543191	intron-variant	ANKRD13B	GRCh38.p7	17:29604383	GGCTAATTTTTTGTA[-/T]TTTTTTGTAGACATG	124930
rs553059192	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29595743	GATCCAGGCCAGGGG[A/G]AATATAGGGCACTGG	124930
rs553065249	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29599465	TAGTGGAAACTGGGC[A/G]GCTTCTAGGTCTGTT	124930
rs553228754	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29596458	CATGGCCAGCTGGGC[A/G]TGGTCCTGGTTCTGG	124930
rs553298307	snp	A/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29597888	CAGCCGCTCTCTGGA[A/G]CCTGGAGCTGAGGCA	124930
rs553384833	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29593118	AGCTCTACCCGGGGC[G/T]CCTGGTCCCCTTCCT	124930
rs553520963	snp	A/T	0.000798403	0.0199641	intron-variant	ANKRD13B	GRCh38.p7	17:29601386	CCCACCACGCCCAGC[A/T]AATTTTTGTATTTTT	124930
rs553562162	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29604193	AGGTAAATTACTTGC[A/G]AATCAGTTTGACCTT	124930
rs553633183	snp	A/G	0.000798403	0.0199641	intron-variant	ANKRD13B	GRCh38.p7	17:29605903	GAGTTACATGCATGT[A/G]GTCAGTTCACTGTTC	124930
rs553633699	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29610957	AGTACTAAGAAGTTT[C/T]TAAGGACTCATCTGG	124930
rs553990449	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29607678	TGCTCCAGGGCTGTC[C/T]GGCTCCGGAGGGCTG	124930
rs553994971	snp	C/T	0.00119737	0.0244387	intron-variant	ANKRD13B	GRCh38.p7	17:29603055	GGGGTTTCACCATAT[C/T]GGCCAGGCTGGTCTC	124930
rs554055948	snp	C/T	0.000798403	0.0199641	intron-variant	ANKRD13B	GRCh38.p7	17:29600386	GTCTTTGGGACAACT[C/T]CCTACTCGGGTAGAT	124930
rs554202299	snp	A/G	0.000595888	0.0172508	synonymous-codon, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29613396	GCCTGCGCCCCCGGC[A/G]TCAGTGCCCAGCCCT	124930
rs554231688	snp	C/G	0.00159617	0.0282053	intron-variant	ANKRD13B	GRCh38.p7	17:29602352	GTGAGCTGAGATCAC[C/G]CCACTGCACTCCAGC	124930
rs554243918	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29595437	AGTCCCACTCCCTTG[C/T]CTGAGGGTGGGTGGT	124930
rs554324552	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29606014	GCCTCCCGGGTTCAA[A/G]CGGTTCTCTTGCCTC	124930
rs554443977	snp	G/T			intron-variant	ANKRD13B	GRCh38.p7	17:29607624	CCTTGTGAGGTTGGT[G/T]AGGCAGAGCAGCCCC	124930
rs554489645	in-del	-/G	0.00119737	0.0244387	utr-variant-3-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29613887	GCCAGGCGGTCCTGA[-/G]GGGGGAGATGAATCC	124930
rs554517543	snp	A/T			intron-variant	ANKRD13B	GRCh38.p7	17:29603833	TTTCTGAGTTTTGTT[A/T]CTATGAAATTATTTT	124930
rs554725183	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29598178	CCCTTCTCTGTGAGG[A/G]GCCACAGCTCAGAGG	124930
rs555021703	in-del	-/T	0.089084	0.191327	intron-variant	ANKRD13B	GRCh38.p7	17:29604548	TTTTCTTTTCTTTTC[-/T]TTTTTTTTTTTGAGA	124930
rs555378786	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29596622	GGGCAGATTGTGGTC[C/T]CAGAGAATCATTTTC	124930
rs555637001	snp	A/G	0.000798403	0.0199641	intron-variant	ANKRD13B	GRCh38.p7	17:29602167	TTGGGAGGCCGAGGC[A/G]GGCGGATCACGAGGT	124930
rs555701169	in-del	-/TTTC	0.0166325	0.0896639	intron-variant	ANKRD13B	GRCh38.p7	17:29604544	TTCTTTTTCTTTTCT[-/TTTC]TTTTTTTTTTTTGAG	124930
rs555710021	snp	C/T	0.000798403	0.0199641	intron-variant	ANKRD13B	GRCh38.p7	17:29595890	CCTCTCGAGGACTGG[C/T]CCAGAGTGAGGCTTG	124930
rs555767847	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29604822	TGCTGGGATTACAGG[C/T]ATGAGCCACTGCACC	124930
rs555922778	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29607635	TGGTGAGGCAGAGCA[A/G]CCCCAGCAGGGGGTG	124930
rs555972561	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29609642	ACACACACATTTATT[C/T]CTCACAGCAACCCTT	124930
rs555982514	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29592533	GGAGGAACGGAGCTG[C/T]CACCTGCTGCTTTTT	124930
rs556062677	snp	A/C	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29607052	GAGACTCCGTCCCCC[A/C]AAAAAAAACACAAAA	124930
rs556254328	snp	A/G			missense, downstream-variant-500B, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29612750	GCGACCCGGGACGAC[A/G]ACGACGACCTGCTGC	124930
rs556338630	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29610840	CTTCAGTGCTTCCAT[C/T]AGTATTCCCACTGGC	124930
rs556384866	in-del	-/T	0.295854	0.245759	utr-variant-3-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29614236	ATCCCCCAAGGCACA[-/T]TTTTTTTTTTTTTTT	124930
rs556405117	snp	C/G	6.65259e-05	0.00576702	intron-variant	ANKRD13B	GRCh38.p7	17:29609025	AGTGGGGCAGGGTGG[C/G]GACGATGGGAGGCAG	124930
rs556580817	snp	A/T	1.68267e-05	0.00290053	intron-variant	ANKRD13B	GRCh38.p7	17:29608286	CTCTCCCACTTTAGG[A/T]CCTGCGCTTGCTCCC	124930
rs556719958	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29601474	TGACCTGCCCGCCTC[A/G]GCCTCCCAAAGTGCT	124930
rs556743141	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29611016	TTACTAATGTTGCTG[C/T]TGAATTTGGGAGAGG	124930
rs556827388	snp	C/T			intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29599382	GACAATAGAGCCTGG[C/T]AACCGGGGAGCAGCA	124930
rs557116226	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29605177	AACCTTTAATACCTT[A/G]GCTTCCCTGAATCCT	124930
rs557677364	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29597959	CAGGCAGCGGCCTGC[C/T]AGCTCCCTAGGGTCT	124930
rs557689624	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29598854	CCCGGCATAAACAAT[A/G]TACTTCTGCAATGAT	124930
rs557757496	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29610084	GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG	124930
rs558072300	snp	C/T	0.000798403	0.0199641	intron-variant	ANKRD13B	GRCh38.p7	17:29601468	CTCTGGTGACCTGCC[C/T]GCCTCGGCCTCCCAA	124930
rs558158841	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29606491	TGAACCTGGGAGGCG[A/G]AAGTTGCAATGAGCC	124930
rs558160459	snp	C/T	0.000399281	0.0141238	downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	CORO6, ANKRD13B	GRCh38.p7	17:29614307	GTGCAAGCCCTGACT[C/T]CCTCATGGTGCCTCG	124930
rs558221176	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29596136	TGGCATAGCTGCCTC[C/T]TCTTCACTCCAAGAA	124930
rs558361576	snp	C/T	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29599130	CTAAGGAGGTGACAT[C/T]TGAGCAGCAGCCTGA	124930
rs558444029	snp	C/G	0.000153292	0.00875343	synonymous-codon, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29613492	GGCGATGGAACTGTC[C/G]GCGCAGGAGCAGGAG	124930
rs558491019	in-del	-/A	0.00716266	0.059414	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29593798	CCGTCCGGCCTGGGG[-/A]GGGGGTGCGGCGCGG	124930
rs558563630	snp	C/T	0.00199481	0.0315187	intron-variant, utr-variant-5-prime	ANKRD13B	GRCh38.p7	17:29594467	TAAGGCCACGTGGGT[C/T]ACCAGCTTTGGGCTG	124930
rs558625234	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29599783	ATTTTTCCTGAGGAT[A/G]TAAATTACTGTTTTC	124930
rs558685451	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29602977	CTGCCTCAGCCCCCA[A/G]GTAGCTGGGACTACA	124930
rs558722131	in-del	-/AAAC			intron-variant	ANKRD13B	GRCh38.p7	17:29606561	AGACTCTGTCTCAAA[-/AAAC]AAACAAACAAACAAA	124930
rs558965669	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29592933	CCAGCGGGGGAGGTG[C/T]GTCCCAGCCCACCTG	124930
rs559075779	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29592461	CACCCTGGGGTCATT[C/G]AGGAAGGAGACAGTC	124930
rs559179424	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29597135	TTGAGCACAGGCTCT[A/G]CGTCCCTCACCTTCC	124930
rs559355258	snp	G/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29602827	CAAGTTTGGAAAAAT[G/T]TTGGACGTTCTTTCT	124930
rs559369654	snp	A/G	0.00517822	0.0506191	intron-variant	ANKRD13B	GRCh38.p7	17:29602945	CAACCTCCCCTTCCC[A/G]GGTTCAAGCGATTCT	124930
rs559446147	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29609694	AGTATTCCCATTTTA[C/T]GCATGTTTATTGAGT	124930
rs559988836	snp	G/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29596686	CTTCCTGCTTTCCCT[G/T]TTCACCCTTCTGACC	124930
rs560006267	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29591630	ACTGGAGATAAAAGG[A/G]TTTCTGGATTCCCCC	124930
rs560037866	snp	G/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29592579	CTGGTTCTTGCTGGG[G/T]ACAGTGTGCGGGGGG	124930
rs560291663	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant	CORO6, ANKRD13B	GRCh38.p7	17:29615144	GCAGCCCTCGCCCCT[A/G]TCGGTGGAAAGAAGG	124930
rs560501895	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29593948	CGGACTCACCTAGAT[G/T]AGAGTAGAGGCCTCT	124930
rs560559477	snp	A/G	0.00159617	0.0282053	intron-variant	ANKRD13B	GRCh38.p7	17:29594660	CCCGCCTCCAGGGTG[A/G]GCTGCAAGAGCCAGA	124930
rs560639606	snp	C/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29608348	GCGGTTCCCTCTATG[C/G]CTTAGCTCAGCTCAG	124930
rs560705373	snp	A/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29604631	ACTGCAACCTCCGCC[A/T]CCTGGGTTCAAGTGA	124930
rs560708626	snp	G/T			intron-variant	ANKRD13B	GRCh38.p7	17:29600705	CCATCCCCATTGCCT[G/T]CAGGTCCTACCTACA	124930
rs560861259	in-del	-/AAAC	0.00119737	0.0244387	intron-variant	ANKRD13B	GRCh38.p7	17:29606560	AGACTCTGTCTCAAA[-/AAAC]AAACAAACAAACAAA	124930
rs560920620	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29611175	AGATACCGTGTCCGA[A/G]GTGAAAAAGCATAAT	124930
rs560994808	snp	A/G	0.000798403	0.0199641	intron-variant	ANKRD13B	GRCh38.p7	17:29610511	AAAAATGTTTGTTGA[A/G]TGAATAAGTGAATGA	124930
rs561186491	in-del	-/C	0.00953873	0.0683987	intron-variant	ANKRD13B	GRCh38.p7	17:29600022	CTGTGACTACAGGCG[-/C]CCCGCCACCACGCCC	124930
rs561190292	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29605934	CTTTTTTTTTTGAGA[C/T]GGAGTTTTGCTCTTG	124930
rs561321755	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29613650	GAGCCAGACAAACCC[A/C]GGCCTGCGCGCCTGC	124930
rs561403354	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29600119	CTGACCTCGTGATCC[A/G]CCCACCTCGGCCTCC	124930
rs561451070	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29606637	TGCAGGGGCTTGTAA[C/T]CCCAGCTGCTTGGGA	124930
rs561900244	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	ANKRD13B	GRCh38.p7	17:29594515	AACAGGGGAAGGGGG[C/G]ATGTCTTCTGGCCAT	124930
rs561944719	snp	C/T	1.67789e-05	0.00289641	intron-variant	ANKRD13B	GRCh38.p7	17:29608282	TGGGCTCTCCCACTT[C/T]AGGTCCTGCGCTTGC	124930
rs561988207	snp	G/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29602744	TTCATAGGCTGTGAG[G/T]GTCAGAATGTGATGT	124930
rs562063547	snp	C/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29596183	TCCGTGGGCAGGCTT[C/G]GCAGTGCAGCTGGCT	124930
rs562250850	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29597375	ACACTTAAGGGCACA[C/T]GTGAGTACCTATGAG	124930
rs562392739	snp	C/T	0.00398564	0.0444627	intron-variant	ANKRD13B	GRCh38.p7	17:29606157	CTCAGGTGATCTACC[C/T]GCCTCGGCCTCCCAA	124930
rs562619178	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29604946	TGAGGTCTGATTAAA[C/T]ATGCATCTCCACTCT	124930
rs562706819	snp	C/T	1.72513e-05	0.0029369	missense, utr-variant-5-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29608105	CTCCTGGAGAAGCTG[C/T]GCAAGGTGAGGCCCA	124930
rs562714140	snp	A/G	0.00279162	0.0372561	utr-variant-3-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29613754	TCGGCATGGCCGCGG[A/G]GTACCTTCCCAGGCC	124930
rs562884665	snp	C/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29607381	CTTGGCCAACAGCCT[C/G]TTTGCCACCCCACTT	124930
rs562908331	in-del	-/A	0.00159617	0.0282053	intron-variant	ANKRD13B	GRCh38.p7	17:29606892	ATCTCTACTAAAAAT[-/A]ACAAAAAATTAGCCA	124930
rs562932712	snp	C/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29600810	GCTTCCTCTGCTCCC[C/G]TAAGTCAGTTGTGAG	124930
rs562996169	snp	C/G	0.00716266	0.059414	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29593799	CGTCCGGCCTGGGGA[C/G]GGGGTGCGGCGCGGG	124930
rs563169232	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant	CORO6, ANKRD13B	GRCh38.p7	17:29615106	TTCTCTCGAGATTTC[C/T]TCGCGGGGGCTGCCG	124930
rs563319345	snp	A/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29603460	GAGACAGAGTCTTGC[A/T]GTATTGCCTGGGCTG	124930
rs563333464	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29604429	GCCCAGGCTGGTCTT[A/G]AACTCCTAGGCTCAA	124930
rs563604762	snp	A/G	0.000798403	0.0199641	intron-variant	ANKRD13B	GRCh38.p7	17:29611256	AGCAAACACACACAC[A/G]CACATGCACACCCCA	124930
rs563907000	snp	C/T	0.00119737	0.0244387	intron-variant	ANKRD13B	GRCh38.p7	17:29597417	GTATCTGTATGGTAC[C/T]AGTGTGTACTAGAGT	124930
rs564151205	snp	A/G	0.00159617	0.0282053	intron-variant	ANKRD13B	GRCh38.p7	17:29600560	CAATTTCTACAAAGA[A/G]TAAACCCCTGGTGTC	124930
rs564213867	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29593319	CCGAGCGGCGTCTTT[C/G]TGTGCGGGGGTGTGG	124930
rs564293284	snp	C/T			intron-variant, synonymous-codon	ANKRD13B	GRCh38.p7	17:29594586	GGCACAGGTCACAGA[C/T]TGCCACTTCTGCCCT	124930
rs564332461	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29592719	GGGGCCAGACCCCTG[A/G]CTGCTCCAATGACCC	124930
rs564354544	snp	A/G	0.00119737	0.0244387	intron-variant	ANKRD13B	GRCh38.p7	17:29597153	TCCCTCACCTTCCTC[A/G]CAAGCACTGTGTTTA	124930
rs564446910	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29612064	CCAGGAGATGCTGGG[A/G]GGCCATGGCTTCCTG	124930
rs564454215	snp	C/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29602541	GACTGGGCCACAACC[C/G]TCTTGGCTTGTGGCT	124930
rs564778232	snp	C/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29611223	ACAACATGAAATCAT[C/G]CCTATGGAAGTGCCT	124930
rs564788442	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29605627	ACAGGCCATCATACC[C/T]GGCTAATTCTTTTGT	124930
rs564790307	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29611824	CAACAAATGAGTTGG[C/T]CTGGCATTAGGAACT	124930
rs564885598	snp	G/T			intron-variant	ANKRD13B	GRCh38.p7	17:29600011	CCTCCCGAGTAGCTG[G/T]GACTACAGGCGCCCG	124930
rs564921209	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29598263	GAAGAAATTCCAGGA[C/T]AAGGCTATAAAAATT	124930
rs565316441	snp	A/G	0.000798403	0.0199641	intron-variant	ANKRD13B	GRCh38.p7	17:29606815	GCACTTTGGGAGCCC[A/G]AGCCAGGTGGATCAC	124930
rs565318023	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant	CORO6, ANKRD13B	GRCh38.p7	17:29614943	GGCTGGGGGTCTCGT[A/T]CCCCTCACTCCCACC	124930
rs565328562	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29607315	TAAATTGGTAGCTCT[C/T]CCTGAAGGTGGCCTG	124930
rs565589743	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29595021	GCAGGCCTCTGGGCC[A/G]GTCTGGGTGGCCACT	124930
rs565656956	snp	C/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29608753	TCAGTTCCCTCCCCT[C/G]TTCCTGGCCACACGG	124930
rs565799040	snp	A/C	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29610048	ATACAAAAAATTAGC[A/C]GGGTGTGGTAGCAGG	124930
rs565945797	snp	C/T	3.37348e-05	0.00410685	intron-variant	ANKRD13B	GRCh38.p7	17:29608133	CCAGCCTCTCAGCCT[C/T]CACGGGAGCCCTTGA	124930
rs566134631	snp	C/T	0.000399281	0.0141238	missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29613403	CCCCCGGCGTCAGTG[C/T]CCAGCCCTCGGCCCA	124930
rs566196337	snp	A/G	0.000798403	0.0199641	downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	CORO6, ANKRD13B	GRCh38.p7	17:29614279	GAGTGTGTCCAACGT[A/G]GCCCCCTGGCCTGTG	124930
rs566310645	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29609705	TTTACGCATGTTTAT[C/T]GAGTCCTTTCCTTGG	124930
rs566721992	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29606281	CTTATGCTTAAGACC[A/G]GGCGTGGTGGCTCAC	124930
rs566994058	snp	A/G	0.00119737	0.0244387	intron-variant	ANKRD13B	GRCh38.p7	17:29607518	GTTACTTTCTGTCCT[A/G]TCTTCTAAGCCCCTT	124930
rs567033842	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29606982	TTGAACCTGGGAGAC[A/G]GAGGTTACAGCGAGC	124930
rs567096546	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29599686	GTCACTTCCAGAATG[A/G]AGAAGGCAAGAGAAA	124930
rs567157658	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29606203	GGCGTGAGCTACCGC[A/G]CCTGGCCTGTCAGTT	124930
rs567189808	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29592891	CTAGGCCCGTGCCCC[C/T]CCACTTCCCCAGCAA	124930
rs567329432	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29609432	CTAAGGTGAGGCTGC[A/G]GCTCCCAGCTGCCAG	124930
rs567390763	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29602984	AGCCCCCAAGTAGCT[A/G]GGACTACAGGTGCCC	124930
rs567496901	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29609969	GAGGCCGAGGTGAGC[A/G]GATCACCTGAGGTCA	124930
rs567521019	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29595927	GATGTACACTGCCTA[C/T]TCCCCAGGGCACCAG	124930
rs567581640	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29596362	CAGCCCGGTGCCCTG[C/T]TTGCCGCTATGCATG	124930
rs567643788	snp	G/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29611374	TTCCTTTTAGTGTTT[G/T]AAGCTGTGCTCACAG	124930
rs567671071	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29598613	GAGTGCAGTAGTGTG[A/G]TCACAGCTCAGTGCA	124930
rs567786820	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29601170	CTCAAGTGATCTGCC[C/T]ACCTCGGCCTCCCAA	124930
rs567971677	snp	A/G	1.72579e-05	0.00293746	intron-variant	ANKRD13B	GRCh38.p7	17:29607963	AGGGTCCTGCCCTGT[A/G]ACCTTGCCTCGCCCT	124930
rs568010594	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29609867	GTTCAGATCCTGGCT[A/G]GCCTGACCCTAGAGC	124930
rs568098076	in-del	-/TG			intron-variant	ANKRD13B	GRCh38.p7	17:29608437	TTATTCTCTTCACTC[-/TG]TCATGATTTGCTTAC	124930
rs568299266	snp	C/T	0.000798403	0.0199641	intron-variant, utr-variant-5-prime	ANKRD13B	GRCh38.p7	17:29594342	AGCGCTCTCCTGCCC[C/T]CTGGTGCTGGGGCCT	124930
rs568299360	snp	A/C	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29601876	GTTTCTGATGAGAAG[A/C]ATATAGTATTTCCTG	124930
rs568313195	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant	CORO6, ANKRD13B	GRCh38.p7	17:29615247	TGTGTCTGCAGAACT[G/T]GGGTGACGCCCATCT	124930
rs568412654	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29605806	TTTTCTCATTGTTTA[C/T]GGTGGCAGAGTAATT	124930
rs568698364	snp	A/G	0.00119737	0.0244387	intron-variant	ANKRD13B	GRCh38.p7	17:29605748	TGCTGGGATTACAGG[A/G]GTGAGCCTCTGTGCC	124930
rs568761780	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29597766	AGCTTGGCTGAGTGT[A/G]TGGGGTTCTGCATGG	124930
rs568989988	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29606796	GCTCACACCTGTAAT[C/T]CCAGCACTTTGGGAG	124930
rs569256494	snp	G/T	0.000798403	0.0199641	intron-variant	ANKRD13B	GRCh38.p7	17:29599566	ACAGTTTTAAAGTTG[G/T]TTTTTTTTTCCACCT	124930
rs569319152	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29592060	TTTAAGTAGGGCCGG[C/T]GTGGAATCCCTTATT	124930
rs569360066	snp	A/T	0.00119737	0.0244387	utr-variant-3-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29614027	CTCCTGGGGGGCAGC[A/T]GAGCTCCCCGCGTGC	124930
rs569421468	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29606861	CAAGACTAGCCTGGC[C/T]AACATGGTGAAAACC	124930
rs569440951	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29606353	CACTTGAGGTCAGGA[A/G]TTAGAGACCAGCCTG	124930
rs569540837	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29599031	TCTGTTCGAGGTGCA[A/G]GAGGTGCTCAACAGG	124930
rs569599451	snp	A/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29595860	TGTAGGTGGGAGAGT[A/T]CCCTAGCTGTCTCCC	124930
rs569656229	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29602944	GCAACCTCCCCTTCC[C/T]GGGTTCAAGCGATTC	124930
rs569785282	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29604702	ACCCATCACCAAGCC[C/T]GGCTAATTTTTTGTA	124930
rs569876749	snp	C/T	0.000463499	0.0152163	synonymous-codon, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29608903	CAAAGTGTGGAAGAG[C/T]GGCCAGAACCTGAGG	124930
rs569937779	snp	C/T	3.36587e-05	0.00410222	synonymous-codon, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29609370	GAACAAGACTGGCAT[C/T]CTGGGCTGGCGCAGT	124930
rs569947329	snp	C/G	0.000798403	0.0199641	intron-variant	ANKRD13B	GRCh38.p7	17:29610123	CTTGAACCTGGGAGG[C/G]GGAGCTTGCAGTGTG	124930
rs570041164	snp	A/C	1.67624e-05	0.00289498	synonymous-codon, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29610762	GCACAAGGGCAAGGT[A/C]AAAGGTAATGAGGCA	124930
rs570123461	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29607044	AACAGAGTGAGACTC[C/T]GTCCCCCCAAAAAAA	124930
rs570187812	snp	A/G	0.00279162	0.0372561	intron-variant	ANKRD13B	GRCh38.p7	17:29607543	CCCCTTTCCATCCAC[A/G]TGTCTGTCTTTCCGT	124930
rs570363958	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant	CORO6, ANKRD13B	GRCh38.p7	17:29615208	TAGCCACTGGGTCCG[G/T]CTCTGCAGCAAACGG	124930
rs570426092	snp	C/T	0.000399281	0.0141238	downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	CORO6, ANKRD13B	GRCh38.p7	17:29614335	TCGGAGAGTGGGGAG[C/T]ATATTGGGCTGGGGT	124930
rs570454023	in-del	-/T			intron-variant	ANKRD13B	GRCh38.p7	17:29596049	GGCCTCTAGTCCCCC[-/T]GGTACCAGCCGCCAC	124930
rs570695700	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29600112	CGATCTCCTGACCTC[A/G]TGATCCGCCCACCTC	124930
rs571017339	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29594077	GGCGACACCTCCCGA[A/G]TGAGGGTGCGGAGGT	124930
rs571073602	snp	A/C	0.00438332	0.0466095	upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29592980	CGCGTCTGGGCCAGG[A/C]CTGACTCCCCGCCCA	124930
rs571391537	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29596478	CCTGGTTCTGGAGTC[A/G]TGAGTTCCTGGTGTT	124930
rs571470263	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29597034	GCCCCTGCACCCCAC[A/G]CTGGGCAGGAGAGGT	124930
rs571535978	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29607586	CTGTCTTTCCGTTGC[C/T]CATAGTGTCTGTCTT	124930
rs571645316	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29606270	ATATTTAAATACTTA[C/T]GCTTAAGACCGGGCG	124930
rs571654737	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29598775	AGGCTGGTCTCGAAC[C/T]CCTGAGCTCAAGTGA	124930
rs571683899	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29593119	GCTCTACCCGGGGCG[C/T]CTGGTCCCCTTCCTC	124930
rs571881949	snp	C/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29611425	TGAAGCACTCAGTCC[C/G]CTTCAGGTGAAGGTG	124930
rs571932725	snp	A/G	7.01681e-05	0.00592276	missense, downstream-variant-500B, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29612663	CCAGCCTCCTGCCGC[A/G]GCTGCGAGATCTCCC	124930
rs572106601	snp	C/G	0.00068698	0.0185207	missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29609092	GTCTGGCAGACACAA[C/G]CGCCGTGGTCATGGA	124930
rs572192958	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29607162	TATAGGATTTGTACA[A/G]ATTTTAATGCATAGT	124930
rs572207159	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29599945	GCAGTGGCGCAATCT[C/T]GGCTCACTGCAAGCT	124930
rs572270274	snp	C/G	0.00199481	0.0315187	intron-variant	ANKRD13B	GRCh38.p7	17:29607681	TCCAGGGCTGTCTGG[C/G]TCCGGAGGGCTGCCT	124930
rs572421198	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29595502	CCCTGGGAGAAAAGA[C/T]TTCTCCAGCAGGCCT	124930
rs572441217	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29608370	TCAGCTCAGGGCCAC[C/T]GCCTCAGCTAGGCCT	124930
rs572467702	snp	C/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29603090	TCCTGATGTTGTGAT[C/G]CACCCGCCTTGGCCT	124930
rs573356638	snp	C/T	0.00119737	0.0244387	intron-variant	ANKRD13B	GRCh38.p7	17:29597154	CCCTCACCTTCCTCG[C/T]AAGCACTGTGTTTAG	124930
rs573451146	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29600299	CTCAGGGATGTGTGG[A/G]TGCTACTGTAAGGTG	124930
rs573679590	snp	A/G	0.00199481	0.0315187	intron-variant	ANKRD13B	GRCh38.p7	17:29596652	CCTTCTCCCTGGGGC[A/G]TTCTCCACCGTGGGC	124930
rs573739221	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29597226	AAGGATTCTGCTCAT[A/G]CTAAAGGAGTTTGGA	124930
rs573758107	snp	A/G	0.00795532	0.062565	intron-variant	ANKRD13B	GRCh38.p7	17:29602223	ACACGGTGAAACCCC[A/G]TCTCTACTAAAAATA	124930
rs573859674	snp	A/G	0.000399281	0.0141238	intron-variant, synonymous-codon	ANKRD13B	GRCh38.p7	17:29594552	GGATGTCTTCTGGCC[A/G]TGCTTCAGAACAAAG	124930
rs574073863	snp	A/T	0.000798403	0.0199641	intron-variant	ANKRD13B	GRCh38.p7	17:29599904	TTTTTTGATACGGAG[A/T]CTCGCTCTGTCCCCC	124930
rs574104146	snp	A/G	0.000798403	0.0199641	intron-variant	ANKRD13B	GRCh38.p7	17:29600307	TGTGTGGGTGCTACT[A/G]TAAGGTGATCAGGTG	124930
rs574142547	snp	A/G	0.00159617	0.0282053	intron-variant	ANKRD13B	GRCh38.p7	17:29609662	CAGCAACCCTTTCTG[A/G]TAGGTGCTGTTCTGT	124930
rs574181860	snp	A/T	0.00398564	0.0444627	intron-variant	ANKRD13B	GRCh38.p7	17:29610188	CAGAGCGAGACTCCA[A/T]CTAAAAAAAAAAAAA	124930
rs574243242	snp	A/C	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29604034	GCTCACGTGAGCCAC[A/C]GCACCCTGCCTATAA	124930
rs574335178	snp	A/G	0.0023933	0.0345097	intron-variant	ANKRD13B	GRCh38.p7	17:29607007	GCGAGCTGATATCAC[A/G]TCATTGTACTCCAGC	124930
rs574567497	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29613608	CGGGACCCTCGCCAG[C/T]GCCACGCGCGCCACG	124930
rs574744744	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29608331	TTCTCATAGTTCTTC[C/T]GGCGGTTCCCTCTAT	124930
rs575216103	snp	C/G	0.00318978	0.0398085	intron-variant	ANKRD13B	GRCh38.p7	17:29611127	CACAGATTCTGTATG[C/G]CCATTGATGCCACAC	124930
rs575275889	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29611483	CCCACCCCAGGAACC[A/G]GCCTCCTCCCTAGGT	124930
rs575305096	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29600078	AGACGGGGTTTCACC[A/G]TGTTAGCCAGGATGG	124930
rs575443818	snp	A/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29605199	CTGAATCCTGTCTCC[A/T]TCTTCTCAACTCAGG	124930
rs575905163	snp	C/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29605973	GCTGGAGTGCAGTGG[C/T]ATGATCTCGGCTCAC	124930
rs575905186	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29597517	GACTCCACCTTTTGA[C/T]TCCAGCTGAGGCCTG	124930
rs575978207	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29595182	TCACAGTGCCCCCAG[A/G]AAACAGATGAACAAA	124930
rs576022107	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29603150	CACCGCACCCGGCCT[A/G]TTTCTCTAAATTTGT	124930
rs576149203	snp	C/G			intron-variant	ANKRD13B	GRCh38.p7	17:29608173	CAGTGCAGACTTAGC[C/G]TCTCTCCCCTTCGTC	124930
rs576186589	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29611077	CATTCTAGTCTAGTG[A/G]GACATATCCTAGGTA	124930
rs576192435	snp	G/T	0.000399281	0.0141238	missense, upstream-variant-2KB, intron-variant, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29593730	AAGGAGGTCCGCGCG[G/T]GCCAGGTAGGAGCGC	124930
rs576232137	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	ANKRD13B	GRCh38.p7	17:29594497	GGGCAGTGGTCTCCA[A/G]AAAACAGGGGAAGGG	124930
rs576315467	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29601469	TCTGGTGACCTGCCC[A/G]CCTCGGCCTCCCAAA	124930
rs576428698	snp	G/T	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29606532	CACTGCACTCTAGCC[G/T]GGGTGACACAGTGAG	124930
rs576707433	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29609594	TATATGGATGTATGG[A/G]TGTATACACAGGGCA	124930
rs576761594	snp	A/G	0.00119737	0.0244387	synonymous-codon, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29613495	GATGGAACTGTCGGC[A/G]CAGGAGCAGGAGGAG	124930
rs576763552	snp	G/T	0.000798403	0.0199641	intron-variant	ANKRD13B	GRCh38.p7	17:29606084	CGCCTGGCTAATTTT[G/T]TATTTTTAGTAGAGA	124930
rs576803524	snp	A/G	0.00478085	0.0486577	intron-variant	ANKRD13B	GRCh38.p7	17:29596207	GCTGGCTGAGGAGGG[A/G]GCCAGCATGGCCACC	124930
rs576837873	snp	A/G	0.00159617	0.0282053	intron-variant	ANKRD13B	GRCh38.p7	17:29599804	TACTGTTTTCCCCCA[A/G]AGAGTTTTCTTTTAT	124930
rs577126644	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant	CORO6, ANKRD13B	GRCh38.p7	17:29614998	CTTAGTAAAATATTT[C/T]ATTCAGTACGTCTTG	124930
rs577133990	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29610603	GGACCCTTTGCTACA[A/G]GGAGTGTTCCCAGTG	124930
rs577448158	snp	C/T	0.000129067	0.00803223	intron-variant	ANKRD13B	GRCh38.p7	17:29607706	CTGCCTCCGACGTGA[C/T]TGGGGCTTTATCTTC	124930
rs577744421	snp	C/T	0.000798403	0.0199641	intron-variant	ANKRD13B	GRCh38.p7	17:29596059	CCCCCTGGTACCAGC[C/T]GCCACAGAAACAGCT	124930
rs578117585	snp	A/G	0.000399281	0.0141238	intron-variant	ANKRD13B	GRCh38.p7	17:29596743	GCCCAGGATGTGCGA[A/G]GAGCACCTCAGACCC	124930
rs578135631	snp	A/T			intron-variant	ANKRD13B	GRCh38.p7	17:29607153	TCACAAAATTATAGG[A/T]TTTGTACAAATTTTA	124930
rs745329282	snp	A/T	1.65211e-05	0.00287407	synonymous-codon, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29611589	TGTAGGCTGTAAGAC[A/T]CCTTTGCAGTCCTTC	124930
rs745521454	snp	A/G	2.84823e-05	0.00377364	missense, downstream-variant-500B, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29612455	TTCGGGAACCTCAAC[A/G]GCTGCGACGAACCGG	124930
rs745773883	snp	A/G	9.15206e-05	0.00676402	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29613033	AGCCAGGACACAGCC[A/G]GAGAACCCGCGGGGC	124930
rs745774464	snp	G/T			intron-variant	ANKRD13B	GRCh38.p7	17:29610826	GGAACCAGCTCCCAC[G/T]TCAGTGCTTCCATCA	124930
rs745819151	snp	A/C	0.0001753	0.00936052	missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29613526	AGGCGGCGGCGCGCG[A/C]GCCAGGAGGAGGAGG	124930
rs745828917	snp	C/T	1.70863e-05	0.00292281	intron-variant	ANKRD13B	GRCh38.p7	17:29610781	GGTAATGAGGCAGAG[C/T]TGGATGGGGAGAGGT	124930
rs746009537	snp	A/G	6.67913e-05	0.00577851	intron-variant	ANKRD13B	GRCh38.p7	17:29612043	GGAAGGTGGGGGGCC[A/G]GGGCTCCAGGAGATG	124930
rs746064530	snp	C/T	1.65061e-05	0.00287277	synonymous-codon, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29612254	CCTGCGTCTGCCTCC[C/T]GGCTTCCCAGTTAAG	124930
rs746094787	snp	G/T			intron-variant	ANKRD13B	GRCh38.p7	17:29610063	CGGGTGTGGTAGCAG[G/T]CGCCTGTAATCCCAG	124930
rs746123964	snp	C/G			intron-variant	ANKRD13B	GRCh38.p7	17:29604582	AGTCTTGCTCTGTCA[C/G]CCAGGCCAGAGTGTA	124930
rs746160687	in-del	-/C	1.83656e-05	0.00303026	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612366	CTGAGGTGTGAGGGG[-/C]TGAGTGGTGGCGCCT	124930
rs746211211	snp	A/G	0.00013569	0.00823568	intron-variant	ANKRD13B	GRCh38.p7	17:29608292	CACTTTAGGTCCTGC[A/G]CTTGCTCCCCTGCCT	124930
rs746317648	snp	C/T			upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29592045	TTCTTGGATTGTTGT[C/T]TTAAGTAGGGCCGGT	124930
rs746344270	snp	C/G	3.49969e-05	0.00418297	missense, utr-variant-5-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29607811	ACGCTGGGGCACCTT[C/G]AGTGTGCCCGTGTGC	124930
rs746467491	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29602931	ATCTCGGCTCATTGC[A/G]ACCTCCCCTTCCCGG	124930
rs746480489	snp	A/G			intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29598575	TTTTCATGAGACAGC[A/G]TCTCACTCTGTCACC	124930
rs746582065	snp	A/C	5.73839e-05	0.00535618	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29613017	GATCCTGTCTCCCCT[A/C]AGCCAGGACACAGCC	124930
rs746582156	snp	A/G	1.74233e-05	0.0029515	intron-variant	ANKRD13B	GRCh38.p7	17:29610673	ATGAGCCCTTTCTTC[A/G]TCTGTCCCCAGGTGT	124930
rs746857392	snp	A/G			utr-variant-3-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29613878	CTAGGGCGGAGCCAG[A/G]CGGTCCTGAGGGGGA	124930
rs746896344	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29597301	AAATACGCACACACA[C/T]GTTACACAGGAGTGG	124930
rs746953808	snp	A/C	3.82424e-05	0.00437261	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612879	CTAACGCCCACGCCT[A/C]CCCGCAGGTCACCAT	124930
rs746995710	snp	A/G/T	7.00444e-05	0.0059176	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29607798	GCACCTGGCCACCAC[A/G/T]CTGGGGCACCTTGAG	124930
rs747113285	snp	A/C			downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	CORO6, ANKRD13B	GRCh38.p7	17:29614489	GACTGACTCTAAAAC[A/C]CTTCATCCAATGGTG	124930
rs747179406	snp	A/G	1.65567e-05	0.00287716	missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29611940	CAGAAGAATACTTCA[A/G]CCCCAACTTTGAGCT	124930
rs747287589	snp	A/G	1.66801e-05	0.00288787	intron-variant	ANKRD13B	GRCh38.p7	17:29612040	CTGGGAAGGTGGGGG[A/G]CCGGGGCTCCAGGAG	124930
rs747400330	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29595136	AAAGGCAGTGCTCTG[C/T]AGCCACGAGAAGCCT	124930
rs747437888	snp	A/C	1.94037e-05	0.00311472	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612561	GCTCCACGAGTGAGG[A/C]CCCCCGCGAGAACGC	124930
rs747543951	snp	A/C	1.74351e-05	0.0029525	intron-variant	ANKRD13B	GRCh38.p7	17:29609434	AAGGTGAGGCTGCAG[A/C]TCCCAGCTGCCAGCC	124930
rs747775489	snp	G/T	0.00014092	0.00839287	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612854	GCCACGGGACTCCGC[G/T]CCGCCACGGCTAACG	124930
rs747799243	snp	A/C			intron-variant	ANKRD13B	GRCh38.p7	17:29609343	CTCACCTGGACCACT[A/C]TGCTTCCCCAGGAAC	124930
rs747813610	snp	C/G	1.79293e-05	0.00299405	intron-variant	ANKRD13B	GRCh38.p7	17:29609460	CAGCCCAGCTGCACT[C/G]TTGCCTACAGCAAGC	124930
rs747833118	snp	A/G			upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29593115	ACAAGCTCTACCCGG[A/G]GCGCCTGGTCCCCTT	124930
rs747959522	in-del	-/AAAAA			intron-variant	ANKRD13B	GRCh38.p7	17:29606729	GACCCTGTCTCAAGT[-/AAAAA]AAAAAAAAAAAAAAA	124930
rs747998489	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29595935	CTGCCTACTCCCCAG[A/G]GCACCAGGCTCTGTT	124930
rs748013926	snp	C/T	1.71176e-05	0.00292549	missense, intron-variant, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29611886	TACAGACCCTGATCA[C/T]TCAGACTCTGAGCCA	124930
rs748036366	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29599784	TTTTTCCTGAGGATG[C/T]AAATTACTGTTTTCC	124930
rs748065309	snp	C/G	1.65537e-05	0.0028769	missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29608909	GTGGAAGAGCGGCCA[C/G]AACCTGAGGGTAGAC	124930
rs748067463	snp	C/T	3.3345e-05	0.00408306	intron-variant	ANKRD13B	GRCh38.p7	17:29612025	AGGCCCCTGCCGGTG[C/T]TGGGAAGGTGGGGGG	124930
rs748120012	snp	C/G	3.37775e-05	0.00410945	intron-variant	ANKRD13B	GRCh38.p7	17:29609279	CTCCTTTGAGAGGTG[C/G]GTGGACATGGCCTTG	124930
rs748120455	snp	C/T	4.99388e-05	0.00499669	intron-variant	ANKRD13B	GRCh38.p7	17:29609028	GGGGCAGGGTGGGGA[C/T]GATGGGAGGCAGCCC	124930
rs748170622	snp	G/T	0.000158894	0.00891189	missense, upstream-variant-2KB, intron-variant, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29593661	AGGAAGGGGCCCGAG[G/T]GCAAGTATCCGCTGC	124930
rs748368660	snp	G/T	1.84106e-05	0.00303397	intron-variant	ANKRD13B	GRCh38.p7	17:29607709	CCTCCGACGTGACTG[G/T]GGCTTTATCTTCCAC	124930
rs748478687	snp	C/G	1.66438e-05	0.00288472	intron-variant	ANKRD13B	GRCh38.p7	17:29608155	AGCCCTTGAGCCCTT[C/G]TCCAGTGCAGACTTA	124930
rs748567318	snp	G/T			intron-variant	ANKRD13B	GRCh38.p7	17:29604938	AACCCTTCTGAGGTC[G/T]GATTAAATATGCATC	124930
rs748634943	snp	A/C	1.69433e-05	0.00291056	missense, downstream-variant-500B, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29612525	CCCCAGGCAGCGACT[A/C]CTCCAGCGTCAGCAG	124930
rs748661842	snp	G/T			intron-variant	ANKRD13B	GRCh38.p7	17:29606642	GGGCTTGTAATCCCA[G/T]CTGCTTGGGAGGCTG	124930
rs748722070	snp	A/G	1.68069e-05	0.00289882	synonymous-codon, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29609213	TGAGGAACAGGTGCT[A/G]AGCCGGCTTACCGCG	124930
rs748869297	snp	G/T	1.65225e-05	0.00287419	intron-variant	ANKRD13B	GRCh38.p7	17:29611673	GGGTACCCGTAAGTG[G/T]AGGGATGTGGATGTG	124930
rs748892667	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29596651	TCCTTCTCCCTGGGG[C/T]GTTCTCCACCGTGGG	124930
rs748907749	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29595602	GCTGCAGGTAGAGGT[A/G]TTGGGGGCTGCTCAT	124930
rs748952627	snp	G/T	0.00100654	0.0224111	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612600	CGGCTCTCCCCGGGG[G/T]GGGTGGGAGGGGCGC	124930
rs749011112	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29600711	CCATTGCCTGCAGGT[C/T]CTACCTACACCTTTC	124930
rs749056908	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29599959	TCGGCTCACTGCAAG[C/T]TCCGCCTCCCGGGTT	124930
rs749139132	snp	C/T	6.75699e-05	0.00581209	synonymous-codon, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29613552	GGAGGAGCTGGAGCG[C/T]ATCCTGAGGCTCTCA	124930
rs749211266	snp	C/T	3.31109e-05	0.00406871	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29608206	CCAGGCCCAGGACTT[C/T]TACGTGGAGATGAAA	124930
rs749267731	snp	C/T	1.77313e-05	0.00297747	intron-variant	ANKRD13B	GRCh38.p7	17:29611857	GGGGAGCTCCTGGGC[C/T]CCTCCCCATGTGGTA	124930
rs749329666	in-del	-/GGGAG			intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29593896	CCGGGAAAGGGTGAT[-/GGGAG]CCCCTCCGGCCGGGA	124930
rs749359791	in-del	-/T	1.64849e-05	0.00287092	frameshift-variant, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29612210	CCGTCAGCAATGCGC[-/T]TTTTTGCCAAGCTCC	124930
rs749367550	snp	C/T			upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29591941	GCTGGGGCCTGGCAC[C/T]ACAGGGTGTGGAGGA	124930
rs749384279	snp	C/T	2.00411e-05	0.00316546	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612395	CTAAAGGTTTCCTCA[C/T]CCTCAGAAATCCCGA	124930
rs749423956	snp	A/G	0.000151076	0.00868996	missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29609112	GTGGTCATGGAGATT[A/G]ACCACGACCGCCGGG	124930
rs749479395	snp	G/T	1.68604e-05	0.00290343	synonymous-codon, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29609177	GGACCGGGAGCTGCT[G/T]CTGGCTGCTGCTCAG	124930
rs749529986	snp	A/G	1.85865e-05	0.00304843	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29613053	ACCCGCGGGGCCCTC[A/G]GCAGGGACCCTCCTG	124930
rs749530257	snp	A/G	2.36326e-05	0.0034374	missense, upstream-variant-2KB, intron-variant, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29593652	GCCTCCGCCAGGAAG[A/G]GGCCCGAGGGCAAGT	124930
rs749601495	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29606989	TGGGAGACGGAGGTT[A/G]CAGCGAGCTGATATC	124930
rs749724945	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29606924	ACGTGTTGGCGAATG[C/T]CTGTAATCCCAGCTA	124930
rs749743386	snp	A/G			synonymous-codon, utr-variant-5-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29608041	GCAGCTGGTGCTTCG[A/G]TACCGGGACTACCAG	124930
rs749795431	snp	C/T	1.69006e-05	0.00290689	missense, utr-variant-5-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29608069	CAGCGGGTGGTGAAG[C/T]GGCTGGCGGGCATCC	124930
rs749857310	snp	A/G	1.75792e-05	0.00296467	missense, utr-variant-5-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29607767	AGCAGCTGGATCCCC[A/G]CGGCCGGACTCCCCT	124930
rs750008687	snp	A/G	1.77644e-05	0.00298025	intron-variant	ANKRD13B	GRCh38.p7	17:29611854	TGAGGGGAGCTCCTG[A/G]GCCCCTCCCCATGTG	124930
rs750096228	snp	A/G	5.07954e-05	0.00503936	intron-variant	ANKRD13B	GRCh38.p7	17:29608803	GAGCTGGTCCAGGCC[A/G]TGTAGGCCAGACCAG	124930
rs750136335	in-del	-/C	0.000109335	0.00739295	intron-variant	ANKRD13B	GRCh38.p7	17:29610815	GCAGGACTGCGGGAA[-/C]CAGCTCCCACTTCAG	124930
rs750157893	snp	A/T	3.32336e-05	0.00407624	missense, downstream-variant-500B, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29612497	CGAGGCAGCCCCAGC[A/T]GCGAGACGCCTTCCC	124930
rs750367093	snp	C/T	3.36247e-05	0.00410015	missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29609247	GTCGTCACCACTCAG[C/T]TTGACACCAAGAATA	124930
rs750422688	snp	C/T	5.55859e-05	0.00527161	intron-variant	ANKRD13B	GRCh38.p7	17:29607698	CCGGAGGGCTGCCTC[C/T]GACGTGACTGGGGCT	124930
rs750448867	snp	C/T	1.65581e-05	0.00287728	intron-variant	ANKRD13B	GRCh38.p7	17:29611547	GTGTGTGTGGAGTTG[C/T]GGTGTCCTCTGAGAT	124930
rs750653055	snp	C/G			intron-variant	ANKRD13B	GRCh38.p7	17:29600388	CTTTGGGACAACTTC[C/G]TACTCGGGTAGATAG	124930
rs750657150	snp	C/T	1.69109e-05	0.00290778	intron-variant	ANKRD13B	GRCh38.p7	17:29608130	GGCCCAGCCTCTCAG[C/T]CTCCACGGGAGCCCT	124930
rs750671651	snp	C/T	1.843e-05	0.00303556	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612367	TGAGGTGTGAGGGGC[C/T]GAGTGGTGGCGCCTA	124930
rs750862743	snp	A/C	4.8048e-05	0.0049012	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612966	GCCGACAGGACAGGT[A/C]AGTGCCCGCTGGGCC	124930
rs750876478	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29610191	AGCGAGACTCCATCT[A/G]AAAAAAAAAAAAAAA	124930
rs750915980	snp	C/T	1.6654e-05	0.00288561	missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29610740	GGACAGAACATCTTT[C/T]AGAACAGCACAAGGG	124930
rs750918021	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29611283	CCCACAGTGCCTGCC[A/G]GGGCAGGCGTTTTAC	124930
rs750963844	snp	A/G	0.000134515	0.00819996	missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29609235	CTTACCGCGCCCGTC[A/G]TCACCACTCAGCTTG	124930
rs750991118	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29595014	TGTGCCCGCAGGCCT[C/T]TGGGCCGGTCTGGGT	124930
rs751116833	snp	A/T			intron-variant	ANKRD13B	GRCh38.p7	17:29601999	ACCTTGGTGTAGTTT[A/T]CTTCGTGTTTGTCTT	124930
rs751150890	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29599464	GTAGTGGAAACTGGG[C/T]GGCTTCTAGGTCTGT	124930
rs751229177	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29611237	TGCCTATGGAAGTGC[C/T]TGAAGCAAACACACA	124930
rs751238483	snp	C/T	1.65288e-05	0.00287474	intron-variant	ANKRD13B	GRCh38.p7	17:29611572	TGAGATGCCACATTT[C/T]TTGTAGGCTGTAAGA	124930
rs751242188	snp	C/T	0.000165886	0.00910578	intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29593743	CGGGCCAGGTAGGAG[C/T]GCCTTCGGGGCGCCG	124930
rs751257805	snp	A/C	0.000131976	0.00812223	synonymous-codon, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29612239	CCGGGACTTCATCAC[A/C]CTGCGTCTGCCTCCT	124930
rs751259426	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29603694	CATTTCAGTTACTGT[A/G]CTTACTATCTTTAGA	124930
rs751487948	snp	A/C/T			upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29591776	CCTCAACCGCGCCAG[A/C/T]CCCCTCCCCTGCACT	124930
rs751628705	snp	C/T	1.87841e-05	0.00306459	synonymous-codon, nc-transcript-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612931	CAAGCCAGGCACCCA[C/T]CCCATGTCCTACGAG	124930
rs751777513	snp	A/G	1.67652e-05	0.00289522	missense, utr-variant-5-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29608018	AGTACCCGGGACCTG[A/G]AGCTGGTGCAGCTGG	124930
rs751805246	snp	C/G			missense, utr-variant-5-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29607763	ATCGAGCAGCTGGAT[C/G]CCCGCGGCCGGACTC	124930
rs751825001	snp	A/G	1.66427e-05	0.00288462	missense, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29610719	TGGAGCTCATCACCC[A/G]CACACGGACAGAACA	124930
rs751850436	snp	C/G	1.6591e-05	0.00288015	intron-variant	ANKRD13B	GRCh38.p7	17:29608997	TTCAGGGGCCAAGGT[C/G]AGGCAGGCAGGAAGT	124930
rs751932192	in-del	-/T			intron-variant	ANKRD13B	GRCh38.p7	17:29600922	AAATATTTTACTGAC[-/T]TTTTTTTTTTTTTTT	124930
rs751956122	snp	C/T			utr-variant-3-prime, intron-variant, downstream-variant-500B, nc-transcript-variant	CORO6, ANKRD13B	GRCh38.p7	17:29614944	GCTGGGGGTCTCGTT[C/T]CCCTCACTCCCACCC	124930
rs752050744	snp	A/G			intron-variant	ANKRD13B	GRCh38.p7	17:29596444	TCCCCCTTGCCTGGC[A/G]TGGCCAGCTGGGCAT	124930
rs752190284	snp	C/T	1.67413e-05	0.00289316	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612318	CCGTGGCGGGCCGAC[C/T]GGGGTTTAGATGAGG	124930
rs752290723	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29611756	CCTTTCCACAATGCC[C/T]AAGGCCATGTCAGCG	124930
rs752298910	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29603996	TCCACCCGCCTCAGC[C/T]TCCCAAAATGCTGGG	124930
rs752377917	snp	A/G	3.07744e-05	0.00392253	intron-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612982	AGTGCCCGCTGGGCC[A/G]GAGAGAATCCTCCGG	124930
rs752384763	snp	A/G	1.67374e-05	0.00289282	synonymous-codon, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29609132	CGACCGCCGGGTGGT[A/G]TACACAGAGACTCTG	124930
rs752449750	snp	C/T	1.79335e-05	0.0029944	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29607867	CAGGGAGAATCGCAG[C/T]GGCTGGACAGGTGGG	124930
rs752479337	snp	G/T			intron-variant, utr-variant-5-prime	ANKRD13B	GRCh38.p7	17:29594526	GGGGGATGTCTTCTG[G/T]CCATGCTTCAGGATG	124930
rs752707834	snp	C/T			intron-variant	ANKRD13B	GRCh38.p7	17:29602295	AGCTACTTGGGAGGC[C/T]GAGGCAGGAGAATGG	124930
rs752741460	in-del	-/TCTCT			intron-variant	ANKRD13B	GRCh38.p7	17:29600881	TCTCATCTGCTGACA[-/TCTCT]TCTCTTTATTCTTGT	124930
rs752789986	snp	A/G	0.000125133	0.00790891	missense, utr-variant-5-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29607863	TGGGCAGGGAGAATC[A/G]CAGCGGCTGGACAGG	124930
rs752902708	snp	C/T	0.00013367	0.00817417	intron-variant	ANKRD13B	GRCh38.p7	17:29609068	CCTGATCCCCCTGTG[C/T]TGTTCCGTGTCTGGC	124930
rs752914703	snp	A/G	3.80431e-05	0.0043612	intron-variant	ANKRD13B	GRCh38.p7	17:29610638	TAGGGGTAAGACACA[A/G]GGTAAGACCAGAACT	124930
rs752965424	snp	G/T	1.90987e-05	0.00309015	missense, nc-transcript-variant, downstream-variant-500B	ANKRD13B	GRCh38.p7	17:29612802	TGCTTGAGGCGGGCA[G/T]TGAGTATGACCAGGT	124930
rs752970572	snp	A/G	1.75323e-05	0.00296072	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29607783	CGGCCGGACTCCCCT[A/G]CACCTGGCCACCACG	124930
rs752990994	snp	C/T			upstream-variant-2KB, intron-variant	ANKRD13B	GRCh38.p7	17:29591840	GGTGCAGGCGGGCAG[C/T]GGTCCCGGGCCCCCG	124930
rs752991406	in-del	-/GCAGCACGG	1.65119e-05	0.00287327	cds-indel, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29611618	CCTGGGAATCGCTGA[-/GCAGCACGG]GCAGCACGGGGGCCC	124930
rs752995277	snp	A/C	8.90813e-05	0.00667328	intron-variant	ANKRD13B	GRCh38.p7	17:29611830	ATGAGTTGGCCTGGC[A/C]TTAGGAACTGAGGGG	124930
rs753056640	in-del	-/C			intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29598115	CACCCAGGTTGCAAG[-/C]CCCCGGAGTCCAGCC	124930
rs753062630	in-del	-/GA			intron-variant	ANKRD13B	GRCh38.p7	17:29595143	GTGCTCTGCAGCCAC[-/GA]GAAGCCTGTTAAAGA	124930
rs753081116	in-del	-/AGG	2.6419e-05	0.00363439	cds-indel, nc-transcript-variant	ANKRD13B	GRCh38.p7	17:29613503	TGTCGGCGCAGGAGC[-/AGG]AGGAGAGGCGGCGGC	124930
rs753095723	snp	C/T			intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29598087	TCCCACTCCCGCTGC[C/T]GGGCTCAGGACCCCA	124930
rs753185551	snp	C/T			intron-variant, upstream-variant-2KB	ANKRD13B	GRCh38.p7	17:29599199	TCCTGGAGAACGTTC[C/T]GGGGAAGGCCATTGG	124930

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