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

FCHSD2

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs1620	snp	A/G	0.0318976	0.122194	intron-variant	FCHSD2	GRCh38.p7	11:73009815	catgctttttttctt[A/G]ctgttttttgaattc	9873
rs152997	snp	A/G	0.0988009	0.199095	intron-variant	FCHSD2	GRCh38.p7	11:72909380	ggtggaggttgtagc[A/G]agccgagatcacgcc	9873
rs429574	snp	A/G/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72909351	GCTCAATGTTGCCCA[A/G/T]GCTGGAGTGCAGTGG	9873
rs479093	snp	C/T	0.00755907	0.0610114	intron-variant	FCHSD2	GRCh38.p7	11:72974529	AGCACTgctgttcaa[C/T]agagttttctaagat	9873
rs493315	snp	A/G	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72970906	AAGGCAATACCAAGA[A/G]GCCAAGTGCAGAAGC	9873
rs494413	snp	C/T	0.00914312	0.0669923	intron-variant	FCHSD2	GRCh38.p7	11:72977628	ctgccgaagcgagca[C/T]GCtctcacaccagtt	9873
rs508532	snp	A/C	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72981137	TACTGTACATTAACT[A/C]ATTTTCTTCCTCATG	9873
rs509597	snp	C/G	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:72975511	taggagagaagattt[C/G]gaaatgttctcaaca	9873
rs537980	snp	C/T	0.00716266	0.059414	intron-variant	FCHSD2	GRCh38.p7	11:72980199	CCCCCTCTTCAAACC[C/T]CAAACTTACCCCTTC	9873
rs555773	snp	A/G	0.0988009	0.199095	intron-variant	FCHSD2	GRCh38.p7	11:72973166	TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGACCA	9873
rs560258	snp	A/G	0.00716266	0.059414	intron-variant	FCHSD2	GRCh38.p7	11:72973637	GGGGTCACCTGGGAG[A/G]TTTCCACTGTACTGA	9873
rs573529	snp	G/T	0.137187	0.223099	intron-variant	FCHSD2	GRCh38.p7	11:72976504	aggctggtctcaaac[G/T]cttggactcaagtga	9873
rs593301	snp	C/T	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:72980296	AAGCAGTGTTGAAAC[C/T]GCTGCACTGGTTTCT	9873
rs593753	snp	C/T	0.297128	0.245518	intron-variant	FCHSD2	GRCh38.p7	11:72980395	CAGATTATCCAGTTA[C/T]GGGGGCTCATCAGAG	9873
rs640283	snp	C/T	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:72971714	TCTTCCCCAGAATCT[C/T]CAGATAAGAATGCAG	9873
rs658164	snp	A/G	0.00716266	0.059414	intron-variant	FCHSD2	GRCh38.p7	11:72977623	atgtgctgccgaagc[A/G]agcatgctctcacac	9873
rs671766	snp	A/G	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:72972713	ACCAATGTAGCAGGG[A/G]AAGAATCTATTACCC	9873
rs724673	snp	C/T	0.333952	0.235483	intron-variant	FCHSD2	GRCh38.p7	11:73084663	CCCATGCCAGTAATC[C/T]CAATGCTTTGGGAGG	9873
rs898384	snp	C/T	0.0854556	0.188216	intron-variant	FCHSD2	GRCh38.p7	11:72985604	CTTCTATTATTTCCA[C/T]CATTAAAAGTACTTC	9873
rs975261	snp	A/G	0.0869089	0.189476	intron-variant	FCHSD2	GRCh38.p7	11:72953443	TGTTTTACAAGGAGT[A/G]CTAGTGTCAAATAAG	9873
rs994305	snp	A/G	0.0178098	0.0926698	intron-variant	FCHSD2	GRCh38.p7	11:72886273	GTATTTCCCAATACT[A/G]AACTCACATCTCCTT	9873
rs1025411	snp	C/G	0.0178098	0.0926698	intron-variant	FCHSD2	GRCh38.p7	11:72955104	gttagcagtctgtga[C/G]acctgacgctctcca	9873
rs1031706	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72975044	TTTTTGGAATTAATG[C/T]TTAGCCAGAAAAACC	9873
rs1045315	snp	C/G	0	0	missense, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841516	ACCAGCCTCCCAGCA[C/G]CCCCTACCCCAGCCC	9873
rs1045372	snp	A/C	0	0	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72836863	ATGGAATCCAGCACC[A/C]CAGTGCACAGGTCAG	9873
rs1062909	snp	G/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838452	CAGTCCCTAAATTAC[G/T]GATCATGTGCACTCG	9873
rs1062910	snp	G/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838373	TCTTCAAGTGGCTTT[G/T]GCTCATCTGATTGAG	9873
rs1065100	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73078633	TTTTTTTTTTTTATC[A/G]GAATAGTTGTTATTT	9873
rs1290092	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72857649	cagcctggccaacat[A/G]gtgaaacccccgtct	9873
rs1298094	snp	A/C	0	0	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838251	AGTCCAATTTTTCCC[A/C]ATAAGGTTTCACTTT	9873
rs1299173	snp	G/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72890947	TTCATTCTACAATTT[G/T]GCTGCTTTCTATATT	9873
rs1367698	snp	C/G	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:72863831	CCTTATCAGTACTTA[C/G]TATAGTCAGTCTTTT	9873
rs1367699	snp	A/C	0.225005	0.248747	intron-variant	FCHSD2	GRCh38.p7	11:72863755	TTTTAATTTCCATTT[A/C]TCTGATAATGTTGAT	9873
rs1380574	snp	C/T	0.097727	0.198275	intron-variant	FCHSD2	GRCh38.p7	11:73085166	CCTTAAACCTAAAGA[C/T]TCATGCTTATTCAAG	9873
rs1380575	snp	C/T	0.0482946	0.147699	intron-variant	FCHSD2	GRCh38.p7	11:73085383	TAACCATTTTGGAAC[C/T]AGGAGTCAACTGAAA	9873
rs1460035	snp	A/G	0.0284301	0.115788	intron-variant	FCHSD2	GRCh38.p7	11:73015315	ATAATACTTATTTTA[A/G]AAAAATATATGTGTT	9873
rs1612659	snp	A/G	0.42574	0.177808	intron-variant	FCHSD2	GRCh38.p7	11:73124258	gtccccccatcccac[A/G]ataggccctggtgtg	9873
rs1614447	snp	G/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72890881	AAAAACAAACTTTAT[G/T]GAGATAATTAGGaat	9873
rs1619988	snp	C/G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73128398	CACCACTACCTTTTT[C/G/T]GTTTGTTGGCAAGGA	9873
rs1783598	snp	A/G	0.342806	0.232136	intron-variant, upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73140418	TAGGAAGACCTAGAC[A/G]TGGATTGAGCTTGTG	9873
rs1785207	snp	C/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72898275	ATAAAATGTAACTCT[C/T]CTGATGATTTTCATA	9873
rs1785208	snp	C/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72897337	CAGACACAACTATCC[C/T]TTTTTTTTTTTTTTT	9873
rs1785209	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72882282	cctgtcttttattac[A/C]agtaaaaaaattagc	9873
rs1785215	snp	A/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72890838	AGAATTTAGAGAGAA[A/T]TAAAATAGTTTTGTG	9873
rs1785216	snp	G/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72888504	ATCCGTCTCATTCTT[G/T]GCCTTCACATCCTGC	9873
rs1785217	snp	A/C	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72920955	CAAGAATATATATAC[A/C]AGAGGCATTCAGGAT	9873
rs1785218	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72851980	ctcctgggctcaagc[A/C]atcttcctgcctcag	9873
rs1785219	snp	A/G	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:72852002	CTGCCTCAGCCTCCC[A/G]AATAGATGGGACTAT	9873
rs1790279	snp	A/C	0.00716266	0.059414	intron-variant	FCHSD2	GRCh38.p7	11:72977390	ACAATCAACAAAGTG[A/C]AGAGACAGCCCATGG	9873
rs1790285	snp	A/G	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72924821	TACATAATTACATGG[A/G]AATCATAGTAATAAT	9873
rs1790286	snp	A/G	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72918344	aattgaaaaagaaga[A/G]ttaaaattacctctc	9873
rs1791053	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73134430	caagctggagcacag[G/T]ggtgtgatcatggct	9873
rs1791054	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73134317	atgcctggctaattt[G/T]gtattttttgtagag	9873
rs1801886	snp	G/T			utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838230	AAATTGGACTGCCCT[G/T]AATTTAGCACCAATT	9873
rs1835644	snp	C/G	0.0988009	0.199095	intron-variant	FCHSD2	GRCh38.p7	11:72948162	AAATTTGCCAGGTCT[C/G]GTGGCACATGCCTGT	9873
rs1982038	snp	A/G	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:72844500	TCCCTGACAGCAGCA[A/G]TCCACCAGCATCAGC	9873
rs1982585	snp	C/T	0.499053	0.0217445	intron-variant	FCHSD2	GRCh38.p7	11:73071429	GGGCGCAGTGGCTCA[C/T]GCCTGTAATCCCAGC	9873
rs1989449	snp	C/T	0.282105	0.24793	intron-variant	FCHSD2	GRCh38.p7	11:73084945	CCTCCTTCTTACTCT[C/T]ATGTCTTTGGTCTTT	9873
rs2003368	snp	A/G	0.377582	0.214995	intron-variant	FCHSD2	GRCh38.p7	11:73129061	ACATGGTGAAATCTC[A/G]TCTCTACTAAAAATA	9873
rs2032351	snp	C/G/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73045152	ttttttcatgtgttt[C/G/T]ttggctgcataaatg	9873
rs2043156	snp	C/G	0.00636936	0.0560724	intron-variant	FCHSD2	GRCh38.p7	11:72874614	AGAATGTAGTGAATA[C/G]TTCTCTCTTTTCTGC	9873
rs2060071	snp	A/T	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:72932315	CCAACTCATTTCCAC[A/T]CTGCAGCTAGGAGGA	9873
rs2060072	snp	C/T	0.0588605	0.161139	intron-variant	FCHSD2	GRCh38.p7	11:72896192	ACTAAATTTCTGATG[C/T]ATGATCTTTCCCTGT	9873
rs2060073	snp	C/T	0.00716266	0.059414	intron-variant	FCHSD2	GRCh38.p7	11:72857572	acacacctgtagtcc[C/T]agctactccggaggc	9873
rs2187494	snp	A/G	0.443195	0.158668	intron-variant	FCHSD2	GRCh38.p7	11:73094558	TATTTATTCTTAAAT[A/G]GAGTAAAGCTCAGTA	9873
rs2276379	snp	A/G	0.499053	0.0217445	intron-variant	FCHSD2	GRCh38.p7	11:73047308	CTTCCCTATCATTTA[A/G]GTATGTAGCTTCTAC	9873
rs2365906	snp	A/G	0.0178098	0.0926698	intron-variant	FCHSD2	GRCh38.p7	11:72854437	TCTGTCTACCTATCT[A/G]TCTATCTGGTTAgag	9873
rs2365907	snp	G/T	0.00756178	0.0610554	intron-variant	FCHSD2	GRCh38.p7	11:72878553	ctgtgatagcttgtt[G/T]tactaggaagaaagt	9873
rs2365908	snp	A/G	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:72880991	atttttatggctgag[A/G]ctttaaggccacagg	9873
rs2365909	snp	A/C	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:72881074	cagcaaaggaaacaa[A/C]agagttaacagatga	9873
rs2366252	snp	C/G	0.0123036	0.0774623	intron-variant	FCHSD2	GRCh38.p7	11:73034956	GCAGGTGACATTTAT[C/G]CTATAGTACTTTAGC	9873
rs2366256	snp	A/G	0.369754	0.219451	intron-variant	FCHSD2	GRCh38.p7	11:73109675	ACTTTTTCCCTTTCC[A/G]CTTTGGATGCTCTTT	9873
rs2446746	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72981874	TGGTCCTAGCTACAT[A/G]GGAGGCTGAGGCAAG	9873
rs2886599	snp	A/C	0.190205	0.242744	intron-variant	FCHSD2	GRCh38.p7	11:73010226	TTCATTCAATGAATT[A/C]TTCCATTACAGAATT	9873
rs3018279	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73131701	ttttttttttttgga[A/G]acatagtctgggttg	9873
rs3018280	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73131691	ttggaaacatagtct[G/T]ggttggtggcctaaa	9873
rs3018281	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73131550	tgcccAGATATTTTT[G/T]GTAGTAAtttttatt	9873
rs3039677	in-del	-/CT	0.0341408	0.126114	intron-variant	FCHSD2	GRCh38.p7	11:72985692	GAGAAAGTCCTGGGA[-/CT]CTCTGCCCTGTATGA	9873
rs3040733	in-del	-/TATTA			intron-variant	FCHSD2	GRCh38.p7	11:73033994	GGTATTAAAATTGTC[-/TATTA]TATTTTCATGATTTC	9873
rs3133221	snp	A/C	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73128012	GAAAAAGACCATTTC[A/C]AAAAAAAAAAAAAAA	9873
rs3207374	snp	A/G	0.0429648	0.14013	intron-variant	FCHSD2	GRCh38.p7	11:72924833	CTCTGGTTATGTTAC[A/G]TAATTACATGGAAAT	9873
rs3207375	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72924762	AATGGTGTCATCTAG[C/T]GGTGTAAGCACTATA	9873
rs3217361	in-del	-/GGG	0.372547	0.217904	intron-variant, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72843362	CAAAACAAGTTTACA[-/GGG]CACACAATTTAGACA	9873
rs3223742	microsatellite	(CA)20/21/22/23/24/27	0.683178	0.165982	intron-variant	FCHSD2	GRCh38.p7	11:72959855	GGTATATTGATATNA[(CA)20/21/22/23/24/27]CCTAGAAACTTAAAA	9873
rs3814729	snp	C/T	0.00279162	0.0372561	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838441	AATATACTGTACGAG[C/T]GCACATGATCAGTAA	9873
rs3814730	snp	A/G	0.222333	0.248464	intron-variant	FCHSD2	GRCh38.p7	11:72844508	AGCAGCAATCCACCA[A/G]CATCAGCCACCCACA	9873
rs3862796	snp	C/T	0.297128	0.245518	intron-variant	FCHSD2	GRCh38.p7	11:72994477	TTAAATAATTTACTC[C/T]GAGTCACACGGCAAG	9873
rs3903492	snp	A/G	0.0178098	0.0926698	intron-variant	FCHSD2	GRCh38.p7	11:72956524	agagaaattaatgct[A/G]ttgattataagtcaa	9873
rs4102512	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72994592	CTcacggtgaaaccc[C/T]gtctctactaaaaat	9873
rs4329714	snp	A/T	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:72965562	AAACTCAATATTTTC[A/T]TGTATTTATTTCTGA	9873
rs4373969	snp	A/G	0.0182019	0.0936463	intron-variant	FCHSD2	GRCh38.p7	11:72914101	ctcgctgcaaactgc[A/G]cttcctgggttcaag	9873
rs4394861	snp	C/T	0.457271	0.139781	intron-variant	FCHSD2	GRCh38.p7	11:73089925	AAAAGCCTACCCTTA[C/T]CAGATGTTAAAAATT	9873
rs4400839	snp	G/T	0.361474	0.223771	intron-variant	FCHSD2	GRCh38.p7	11:72964620	CTTCTATCATCATCA[G/T]CAGCAGCAGAATCTT	9873
rs4465389	snp	A/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72954197	cagtagatgtgggga[A/T]ttttttttttttttt	9873
rs4480564	snp	C/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72932177	TTATTGATTCCACTT[C/T]TTAAATATTTACCAA	9873
rs4515995	snp	A/G	0.404035	0.196909	intron-variant	FCHSD2	GRCh38.p7	11:72976750	cagaatcaaatccat[A/G]catctacagtgaact	9873
rs4578418	snp	G/T	0.143284	0.226079	intron-variant	FCHSD2	GRCh38.p7	11:72980647	CTAATTTGCAATCAT[G/T]TATATATGTATGTGT	9873
rs4594026	snp	A/G	0.0178098	0.0926698	intron-variant	FCHSD2	GRCh38.p7	11:72964552	TTTTGTTGCCTTTTC[A/G]TCTGGAGTCTAGCAG	9873
rs4643105	snp	C/T	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:72964505	AACAGTACACATCTG[C/T]CTTCTTCATTCCTTA	9873
rs4944015	snp	A/G	0.0178098	0.0926698	intron-variant	FCHSD2	GRCh38.p7	11:72846162	TACTCATGATGAGTA[A/G]GCTGCTCCTCCTTTT	9873
rs4944016	snp	C/T	0.348794	0.229651	intron-variant	FCHSD2	GRCh38.p7	11:72886393	ATACTATTCATCTGC[C/T]AGCATTCATCTTAAG	9873
rs4944017	snp	C/T	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:72903144	GAGGTTACACTCTAA[C/T]TACCATCTTACAGCA	9873
rs4944018	snp	C/T	0.0998734	0.199905	intron-variant	FCHSD2	GRCh38.p7	11:72903317	CGCCTCCCGGGTTCA[C/T]GCCATTCTCCTGCCT	9873
rs4944019	snp	A/G	0.0984431	0.198823	intron-variant	FCHSD2	GRCh38.p7	11:72904495	aaacatccccttatg[A/G]ccaatattctttcat	9873
rs4944020	snp	C/T	0.00394476	0.0442359	intron-variant	FCHSD2	GRCh38.p7	11:72943402	AGAATTCCAAGATGT[C/T]TGATGGAGAGGTTTG	9873
rs4944811	snp	A/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72866038	AAAGTCAGATGGTAT[A/G]TGGCCCCTCAATTGA	9873
rs4944812	snp	A/C	0.00517822	0.0506191	intron-variant	FCHSD2	GRCh38.p7	11:72873943	ATGATCCAAAAAAGG[A/C]TACTACCGTGCCACT	9873
rs4944813	snp	C/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72880303	gaaccacaaaagtcc[C/T]tgaatagccaaagca	9873
rs4944814	snp	C/T	0.0980852	0.198549	intron-variant	FCHSD2	GRCh38.p7	11:72894411	ATACCTGTAGTCCTA[C/T]CTATGGGAGGCTGAG	9873
rs4944815	snp	A/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72903207	TATTTATTTATTTAT[A/T]TATTTATTTATTTAT	9873
rs4944816	snp	A/G	0.498794	0.0245311	intron-variant	FCHSD2	GRCh38.p7	11:72903374	GGCGCCCGCCACTGC[A/G]CCCAGCTAATTTTTT	9873
rs4944817	snp	C/T	0.0178098	0.0926698	intron-variant	FCHSD2	GRCh38.p7	11:72931904	ATTCTGGGTCAATGC[C/T]ATTGTTTCATTGTTG	9873
rs4944818	snp	A/G	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:72949063	accattaagttaatc[A/G]ttttaaagtatacaa	9873
rs4944820	snp	C/G	0.0283406	0.115616	intron-variant	FCHSD2	GRCh38.p7	11:73096196	TGCTGTCATGAAAGA[C/G]ATAATATGTAACCAA	9873
rs4944822	snp	G/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73118503	aattctggagtatag[G/T]atacagtatatattc	9873
rs4944823	snp	A/G	0.454544	0.143743	intron-variant	FCHSD2	GRCh38.p7	11:73120169	tccctcccacaacac[A/G]tgggaattatgggaa	9873
rs4944824	snp	C/T	0.0170251	0.090679	intron-variant	FCHSD2	GRCh38.p7	11:73124928	TAGAGCAAGGGAAAG[C/T]ACATTCCATAGATGT	9873
rs5792604	in-del	-/AT			intron-variant	FCHSD2	GRCh38.p7	11:72887128	TTGATATATAAGGAG[-/AT]ATATATATATATATC	9873
rs5792606	in-del	-/T	0.0244538	0.107838	intron-variant	FCHSD2	GRCh38.p7	11:72892908	GGTAATTTTTTTTTT[-/T]AAGACAGTGATATTA	9873
rs5792607	in-del	-/A	0.220544	0.248259	intron-variant	FCHSD2	GRCh38.p7	11:72953628	GGGGGAAAAAAAAAA[-/A]CACAAAAACTCTTGC	9873
rs6421714	snp	A/G	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:72914352	aatgctattcccatt[A/G]aactaccattgacat	9873
rs6592492	snp	A/G	0.00557542	0.0525036	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72837551	ACAGGAGCGGACAGC[A/G]GACAGTCAGCACCTG	9873
rs6592493	snp	C/T	0.00557542	0.0525036	intron-variant	FCHSD2	GRCh38.p7	11:72851219	gaaaaaacaacctgt[C/T]cactgaaattaaaaa	9873
rs6592494	snp	A/G	0.102014	0.201495	intron-variant	FCHSD2	GRCh38.p7	11:72851263	tgatctagcaattcc[A/G]cttttatgaatacat	9873
rs6592495	snp	C/T	0.0471551	0.14613	intron-variant	FCHSD2	GRCh38.p7	11:72912360	tatcataaggggagg[C/T]taaattttatcaaat	9873
rs6592497	snp	A/G	0.0178098	0.0926698	intron-variant	FCHSD2	GRCh38.p7	11:72929169	GCTATTGTGAATAAT[A/G]CCGCTATAAACATAC	9873
rs6592498	snp	C/T	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:72936960	CTTGCCTCCTTTTAT[C/T]CCTGTGTATGGGCTA	9873
rs6592499	snp	C/T	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:72936999	TGTTTCTTTATATGC[C/T]TCATAATCTTGTTAA	9873
rs6592500	snp	A/G	0.456803	0.140473	intron-variant	FCHSD2	GRCh38.p7	11:72940660	CGACCAGGCTGCAAG[A/G]CCAAGCAAGGTTACA	9873
rs6592501	snp	C/T	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:72943094	CCTCCCGGGTTCAAG[C/T]GATTCTCCTTCCTTG	9873
rs6592502	snp	C/T	0.0984431	0.198823	intron-variant	FCHSD2	GRCh38.p7	11:72946677	TTTACCTTTAAAATA[C/T]GATGGTATAAACAGA	9873
rs6592504	snp	C/T	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:72968004	GCTGAGGCAGGAGAA[C/T]GGCGTGAACCTGGGA	9873
rs6592505	snp	C/T	0.367913	0.220446	intron-variant	FCHSD2	GRCh38.p7	11:73000570	TTAGTCAAAATGTGT[C/T]AATTTCCTTTAAATT	9873
rs6592506	snp	A/G	0.281313	0.248031	intron-variant	FCHSD2	GRCh38.p7	11:73035078	gtatactggttaaga[A/G]cacagacacacattc	9873
rs6592507	snp	A/C	0.0223435	0.103308	intron-variant	FCHSD2	GRCh38.p7	11:73045539	tccaacaatgataga[A/C]tggattaagaaaatg	9873
rs6592508	snp	A/G	0.499918	0.00638925	intron-variant	FCHSD2	GRCh38.p7	11:73073628	CCTCACAAACGCTCA[A/G]TCTTTTTAGTCAATC	9873
rs6592509	snp	C/T	0.372592	0.217879	intron-variant	FCHSD2	GRCh38.p7	11:73073864	TGAGCATTGCTGTAA[C/T]CACAGTACCTAGAAG	9873
rs6592510	snp	C/T	0.373598	0.21731	intron-variant	FCHSD2	GRCh38.p7	11:73077778	GAGGGATTATAAGGA[C/T]ACACAGGAAAACTCT	9873
rs7101418	snp	C/T	0.0119091	0.0762411	intron-variant	FCHSD2	GRCh38.p7	11:72948084	gcgatctcggctcac[C/T]gcaacctccacctct	9873
rs7101936	snp	C/G	0.00716266	0.059414	intron-variant	FCHSD2	GRCh38.p7	11:72928117	CATTGGCCACATATT[C/G]ATAATGGTTAAAGCT	9873
rs7102253	snp	C/T	0.298398	0.245271	intron-variant	FCHSD2	GRCh38.p7	11:73081652	ctgcctcagcctccc[C/T]actagctgggattac	9873
rs7102424	snp	G/T	0.0437281	0.141251	intron-variant	FCHSD2	GRCh38.p7	11:72911598	acattttaagaatat[G/T]tattctcccaatcca	9873
rs7104158	snp	A/G	0.499515	0.0155675	intron-variant	FCHSD2	GRCh38.p7	11:73055152	tcgaaagaactcact[A/G]tcatgagaacaacag	9873
rs7105776	snp	A/G	0.107341	0.205301	intron-variant	FCHSD2	GRCh38.p7	11:73013058	AGTAAAGATGATAAT[A/G]TGATTCCTCTCATGG	9873
rs7106212	snp	C/T	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:72912145	gctctttctttcttt[C/T]gtctgactgctgtag	9873
rs7107376	snp	G/T	0.281577	0.247998	intron-variant	FCHSD2	GRCh38.p7	11:72929946	AAACTGAGAAGGGTC[G/T]GAGCTACAAAAGCAG	9873
rs7107817	snp	C/T	0.0966517	0.197444	intron-variant	FCHSD2	GRCh38.p7	11:73138161	GTGTGCCACATCtca[C/T]atgtattgtcatttg	9873
rs7108924	snp	C/T	0.0256215	0.110247	intron-variant	FCHSD2	GRCh38.p7	11:73108875	cgcgcccagcctaga[C/T]ttaagtttttaacac	9873
rs7108955	snp	C/T	0.343477	0.231866	intron-variant	FCHSD2	GRCh38.p7	11:73035205	gtatgtatgtatgta[C/T]gtactaagacaaggt	9873
rs7109082	snp	A/C	0.212425	0.24716	intron-variant	FCHSD2	GRCh38.p7	11:72996396	AACCACAATATTTCA[A/C]GGATGGTAAGTAAAC	9873
rs7110183	snp	C/T	0.221439	0.248363	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72839990	gaggaagaaagcaaa[C/T]gaggcaaatgtagAG	9873
rs7110585	snp	A/G	0.0134861	0.0810011	intron-variant	FCHSD2	GRCh38.p7	11:73127190	ATGGTAACACTTTTC[A/G]TAACACCAGAAATAA	9873
rs7113404	snp	A/G	0.00716266	0.059414	intron-variant	FCHSD2	GRCh38.p7	11:72909594	taggaagtgaggagc[A/G]tctctgcctggctgt	9873
rs7115321	snp	C/T	0.0182019	0.0936463	intron-variant	FCHSD2	GRCh38.p7	11:72871720	GTGAATAGATAGCCA[C/T]TGCACTCCAGTGACA	9873
rs7116176	snp	G/T	0.282369	0.247896	intron-variant	FCHSD2	GRCh38.p7	11:73057127	aaTAAAATCCATAGG[G/T]TGACAATTGATTTGC	9873
rs7117220	snp	A/T	0.0279526	0.114869	intron-variant	FCHSD2	GRCh38.p7	11:73020631	AGGAAAGTTTTAAAA[A/T]ATTCTTCATTGTTCT	9873
rs7117334	snp	C/G	0.0150606	0.0854603	intron-variant	FCHSD2	GRCh38.p7	11:72854794	gaggctgcatgatgg[C/G]gagttattgcttaat	9873
rs7117786	snp	A/T	0.0482946	0.147699	intron-variant	FCHSD2	GRCh38.p7	11:73134074	TGTAACTTACATGAT[A/T]TGTACATTGTATATA	9873
rs7117812	snp	C/T	0.00517822	0.0506191	intron-variant	FCHSD2	GRCh38.p7	11:73133922	atggggagcgactgc[C/T]aatgggtaccaagtt	9873
rs7118144	snp	G/T	0.0930568	0.194599	intron-variant	FCHSD2	GRCh38.p7	11:72987737	GCTGTGGCTAAATTA[G/T]TTGTTTATACATGCT	9873
rs7118154	snp	A/C	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73081794	aactgttgctatttc[A/C]caggtttgaaaggat	9873
rs7120191	snp	A/G	0.00716266	0.059414	intron-variant	FCHSD2	GRCh38.p7	11:72946313	aaaaaaccaaacacc[A/G]catgttctcactcat	9873
rs7121707	snp	C/G/T	0.0821764	0.185298	intron-variant	FCHSD2	GRCh38.p7	11:73038082	ATATTAAAAACAAAA[C/G/T]CATCTATCACTAAAA	9873
rs7122166	snp	A/C	0.0126979	0.078662	intron-variant	FCHSD2	GRCh38.p7	11:72964699	CCAGGTCTTTATGGT[A/C]ATAGCCTTACTGGTA	9873
rs7122194	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73038515	gtggatactatgcag[C/T]catgaaaagaatgaa	9873
rs7122196	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73038516	tggatactatgcagc[C/G]atgaaaagaatgaaa	9873
rs7122566	snp	C/T	0.0494327	0.149241	intron-variant	FCHSD2	GRCh38.p7	11:72951553	TGTGGGATTGTAAAA[C/T]TTATCACCATTTTCC	9873
rs7122570	snp	A/G	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:72934915	TGTTTTAATGACTCC[A/G]CAATATTTTTAAACA	9873
rs7123525	snp	G/T	0.0441095	0.141807	intron-variant	FCHSD2	GRCh38.p7	11:73109629	tttccccaaatataa[G/T]atcaaatcatctgca	9873
rs7124419	snp	A/G	0.00755907	0.0610114	intron-variant	FCHSD2	GRCh38.p7	11:72882169	GAGCAGAggctgggc[A/G]tggtggctcatgcct	9873
rs7124622	snp	C/G	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:72868265	agaaaaccaaacact[C/G]catgttctcacttgt	9873
rs7124723	snp	A/G	0.369142	0.219784	intron-variant	FCHSD2	GRCh38.p7	11:73120189	aattatgggaattca[A/G]gatgagatttgggtg	9873
rs7125633	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72965011	AGCCAGGATGGTCTC[A/G]ATTTCCCAACCTCAT	9873
rs7126070	snp	C/T	0.326976	0.237854	intron-variant	FCHSD2	GRCh38.p7	11:72929026	TGGTTTCCAGCTTCA[C/T]CCATGTCCCTACAAA	9873
rs7127235	snp	A/G	0.0182019	0.0936463	intron-variant	FCHSD2	GRCh38.p7	11:72939712	CAACCCCCGCCTCCC[A/G]GGTTCAAGTGATTCT	9873
rs7127601	snp	C/G	0.00159617	0.0282053	intron-variant, downstream-variant-500B	FCHSD2, ATG16L2	GRCh38.p7	11:72844202	GGAAGCAAAGGCAAA[C/G]GAGAAGGCACTGAAT	9873
rs7128514	snp	A/T	0.446249	0.154875	intron-variant	FCHSD2	GRCh38.p7	11:73035696	actgaaATGTTCAGt[A/T]tttatttatttattt	9873
rs7128993	snp	C/G	0.0825414	0.185628	intron-variant	FCHSD2	GRCh38.p7	11:72980764	TATATATATGTGTAT[C/G]TATATATATACATCT	9873
rs7129171	snp	A/G	0.00636936	0.0560724	intron-variant	FCHSD2	GRCh38.p7	11:72853478	ggagtgtagtggcgc[A/G]atcttgactcactgc	9873
rs7129851	snp	A/G	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:72887659	TTTACATAATTCAAA[A/G]GGCTTTAGTGACTAG	9873
rs7129860	snp	C/T	0.00557542	0.0525036	intron-variant	FCHSD2	GRCh38.p7	11:72847912	TGGTTGGGCCAGTCT[C/T]GAACTCCTAACCTCA	9873
rs7129921	snp	G/T	0.493107	0.0583	intron-variant	FCHSD2	GRCh38.p7	11:72965829	CTTGTGATAAGATTC[G/T]GTTGCTCTACCTCAT	9873
rs7130559	snp	C/T	0.0912534	0.193131	intron-variant	FCHSD2	GRCh38.p7	11:73091631	TTCACATGTTATGCC[C/T]CAGCTAAgtttctta	9873
rs7131604	snp	G/T	0.0123036	0.0774623	intron-variant	FCHSD2	GRCh38.p7	11:72947987	GACATCGTTTGGGTA[G/T]CATACATTttttgtt	9873
rs7350535	snp	C/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73020007	TTTATTTATATTTAC[C/T]TAAGCATCACTGATG	9873
rs7350539	snp	C/T	0.00332778	0.0406548	intron-variant	FCHSD2	GRCh38.p7	11:73020271	GACTGATGGCTTAAC[C/T]TTTGGCCAATTTATT	9873
rs7358314	snp	C/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72951724	ACAAAATTTTTCTTC[C/T]TAAGAGTCTCAATGT	9873
rs7395081	snp	C/T	0.0980852	0.198549	intron-variant	FCHSD2	GRCh38.p7	11:72860078	tccaacctagatccc[C/T]tacatgtgaagttca	9873
rs7478836	snp	A/G	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73046299	ccccagccTCTGTAA[A/G]AATTTTTGAAAAGCC	9873
rs7925155	snp	C/G	0.34146	0.23267	intron-variant	FCHSD2	GRCh38.p7	11:73021385	tgcagccataaaaaa[C/G]aatgagatcatgtcc	9873
rs7925466	snp	A/C	0.487305	0.0786545	intron-variant	FCHSD2	GRCh38.p7	11:73067068	tattcacaatagcaa[A/C]gacttggaaccaacc	9873
rs7925928	snp	A/G	0.487621	0.0776941	intron-variant	FCHSD2	GRCh38.p7	11:73037339	agtgctgtacagtct[A/G]tgtgtctggacaaac	9873
rs7926133	snp	C/T	0.387074	0.209071	intron-variant	FCHSD2	GRCh38.p7	11:72936251	TCCCTTGTAAGCCTA[C/T]AGTAAGGAATTTTGG	9873
rs7930023	snp	C/G	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73123334	TCCTGGAATCCCTGA[C/G]GTCAGGAAAAGTATC	9873
rs7930059	snp	A/C/G	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73123405	TCCTGGAAAagtagc[A/C/G]ctcatccttaattac	9873
rs7930169	snp	C/G	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73123457	gctttttatatatgc[C/G]caggcctctcccaaa	9873
rs7930535	snp	A/G	0.0991586	0.199366	intron-variant	FCHSD2	GRCh38.p7	11:73065214	caacatatgcaaatc[A/G]ataaatgtaatctat	9873
rs7930752	snp	C/T	0.0126979	0.078662	intron-variant	FCHSD2	GRCh38.p7	11:72937749	GAACCTGGGCAAGCA[C/T]TGGAAACAAACAAAC	9873
rs7930893	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73123404	CTCCTGGAAAagtag[C/T]gctcatccttaatta	9873
rs7931372	snp	C/G	0.00557542	0.0525036	intron-variant	FCHSD2	GRCh38.p7	11:72859446	ggccccaaagcacta[C/G]agtagtgctgctggc	9873
rs7931657	snp	A/G	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73052942	accaccgcctcctag[A/G]ttcaggtgattctcc	9873
rs7932028	snp	G/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73053299	tcatacaaaagaaat[G/T]tgtggatctacaacc	9873
rs7932152	snp	A/G	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73053345	aatttaaatttaact[A/G]taattccacaggata	9873
rs7933548	snp	C/T	0.281313	0.248031	intron-variant	FCHSD2	GRCh38.p7	11:73038888	GTAATAAGGCCAATA[C/T]CCATATAAATTATGA	9873
rs7933734	snp	G/T	0.0287284	0.116357	intron-variant	FCHSD2	GRCh38.p7	11:73011396	CCTAGGCTAGCAGGT[G/T]GGGAATACTTGCCCC	9873
rs7935563	snp	A/C	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73057680	caagactcccagttt[A/C]ttcatcatcaacaaa	9873
rs7935982	snp	C/T	0.0448719	0.142907	intron-variant	FCHSD2	GRCh38.p7	11:73112156	aagaactccctttag[C/T]atttcttataggaca	9873
rs7936751	snp	G/T	0.488846	0.0738428	intron-variant	FCHSD2	GRCh38.p7	11:73009154	AACAATTTAAAAGAC[G/T]GATTACATGCACTGT	9873
rs7936855	snp	C/T	0.230603	0.249246	intron-variant	FCHSD2	GRCh38.p7	11:72906272	cccactttttgatgg[C/T]gttgtttttttcttg	9873
rs7936863	snp	A/G	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:72957685	tttcctgatttggat[A/G]gctaggtaagggagt	9873
rs7937701	snp	A/G	0.499954	0.00479211	intron-variant	FCHSD2	GRCh38.p7	11:73121632	CAATAAAGTCTTAAC[A/G]AAGAATCAGTAATTG	9873
rs7937866	snp	A/G	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:72954757	gtatgatgaaagcca[A/G]atttatcaatggtaa	9873
rs7938980	snp	C/T	0.0119091	0.0762411	intron-variant	FCHSD2	GRCh38.p7	11:72962881	ttcagcaggcatCAG[C/T]GGAAGTGACTCTGGA	9873
rs7939641	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73128000	gcctgggcaacagaa[C/T]aagaccatctcaaaa	9873
rs7939736	snp	C/T	0.0441095	0.141807	intron-variant	FCHSD2	GRCh38.p7	11:73015247	TCATTACAATTCGTA[C/T]GTGGGATATTAACTA	9873
rs7939746	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73128048	TCACTGAGAACACAA[C/T]TGCCTGCGGGCCCTT	9873
rs7939875	snp	C/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73128162	ACTCCTAACCTGACA[C/T]ACTTAATTCAAAAGG	9873
rs7940683	snp	C/T	0.0444908	0.142359	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842035	CAAGATCGGCAAACA[C/T]GTTCCTTCTTCCTCT	9873
rs7941209	snp	C/T	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:72850394	ttttttattttattt[C/T]tgagacggagtctcg	9873
rs7941434	snp	C/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72945631	tacagaatgggagaa[C/T]atttttgcaatctac	9873
rs7943424	snp	C/T	0.496937	0.0390173	intron-variant	FCHSD2	GRCh38.p7	11:72898074	GAACAAAGCTTGCCA[C/T]TGGTCACTGTCACTT	9873
rs7944201	snp	A/G	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73052878	ttgagatggagtctc[A/G]ctctgttgcccagac	9873
rs7944277	snp	G/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73026330	gttcatagtatactg[G/T]attcaggattttgct	9873
rs7944808	snp	C/T	0.226188	0.248863	intron-variant	FCHSD2	GRCh38.p7	11:72851055	gtgagccaagaaaga[C/T]tgcaccactgcacta	9873
rs7945119	snp	G/T	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:72888672	CACCCAGTCTGGAGT[G/T]CAGAGGCATGATCTT	9873
rs7945307	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73123260	GACTATCCAATTGAT[A/G]ATTTTATACATCTTG	9873
rs7946019	snp	A/C	0.0973687	0.197999	intron-variant	FCHSD2	GRCh38.p7	11:73065301	gcctttgacaaaatt[A/C]aacagcgcttcatgc	9873
rs7946651	snp	C/T	0.278399	0.248382	intron-variant	FCHSD2	GRCh38.p7	11:73014395	cggcctcccaaagtg[C/T]taggattacaggcat	9873
rs7946861	snp	A/G	0.381891	0.212379	intron-variant	FCHSD2	GRCh38.p7	11:72846941	TTATATGTTATGGCT[A/G]TAGTATATGAATGTC	9873
rs7947165	snp	A/G	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73053008	cccgccaccacacct[A/G]gctaatttttgtatt	9873
rs7947513	snp	A/T	0.00716266	0.059414	intron-variant	FCHSD2	GRCh38.p7	11:73053262	taaaaacattttcaa[A/T]ttttttccaccaaaa	9873
rs7948114	snp	A/G	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73057301	AAGCATGGGCACTGA[A/G]GCCACTAGGAGAAGC	9873
rs7948361	snp	G/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73123250	ATTCAATGTTGACTA[G/T]CCAATTGATAATTTT	9873
rs7948749	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73123568	CGTTCTTGGCATCTA[C/T]ATTTGAATAAGCTAT	9873
rs7948950	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73057252	ATGTCTTTAAGTGAC[C/T]GGCATAGTACCTAGG	9873
rs7948960	snp	C/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73057276	ACCTAGGACACAGTA[C/T]ACAGGTTCGAAGCAT	9873
rs7949675	snp	A/G	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73128111	GAAGTGGTAAGATTG[A/G]GAGGAGAATCCTAAG	9873
rs7951007	snp	C/T	0.00874735	0.0655527	intron-variant	FCHSD2	GRCh38.p7	11:73075898	ccaacgcagtcggat[C/T]gcttgagtccaggag	9873
rs7951253	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73054088	actaaataaagtttg[A/T]ctggaagacagtcac	9873
rs7951491	snp	A/G	0.00438332	0.0466095	intron-variant	FCHSD2	GRCh38.p7	11:72994115	TCACTTGGAGGACCA[A/G]ACAGAATAACTGGTC	9873
rs7951562	snp	C/G	0.0991586	0.199366	intron-variant	FCHSD2	GRCh38.p7	11:72945925	ggatgtggagaaata[C/G]gaacacttttacact	9873
rs7951614	snp	A/G	0.0425829	0.139564	intron-variant	FCHSD2	GRCh38.p7	11:73033753	TTGAGTTTGAGTACT[A/G]TACTGCCTTTGCTGT	9873
rs9645708	snp	C/T	0.480064	0.0978296	intron-variant	FCHSD2	GRCh38.p7	11:73108273	TCTTTTCCTATGAAG[C/T]TGTTTAAGCTCATTA	9873
rs9733917	snp	G/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72944358	TCAACAACGCTTCAT[G/T]CTAAAAACTCTCAAT	9873
rs9733925	snp	C/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72944505	AAGACAGGGATGCCC[C/T]CTCTCACCACTCCTA	9873
rs9733935	snp	C/T	0.00755907	0.0610114	intron-variant	FCHSD2	GRCh38.p7	11:72944655	TCTAGAAAACCCCAT[C/T]GTCTCAGCTCAAAAT	9873
rs9795303	snp	A/G	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:72905736	GAATATTGGTTTCCA[A/G]CTTCATCAATGTCCC	9873
rs10400326	snp	C/T	0.0119091	0.0762411	intron-variant	FCHSD2	GRCh38.p7	11:73088327	ataggctatatcata[C/T]agcttaggtgtgtag	9873
rs10400329	snp	C/T	0.0123036	0.0774623	intron-variant	FCHSD2	GRCh38.p7	11:73088576	TAATTTCTGGTGTTT[C/T]AGTAAACATATAATG	9873
rs10437750	snp	A/G	0.499035	0.0219437	intron-variant	FCHSD2	GRCh38.p7	11:73043000	catgtcatctgcaaa[A/G]aaggacaatttgact	9873
rs10531783	in-del	-/ATAA			intron-variant	FCHSD2	GRCh38.p7	11:72864618	TTAAAAAATAAATAA[-/ATAA]GAGTAAGGAAATACA	9873
rs10579880	in-del	-/TTT			intron-variant	FCHSD2	GRCh38.p7	11:72850078	TTTTTTTTTTTTTTT[-/TTT]GAGATGGAATTTCGC	9873
rs10657358	in-del	-/GAA/GAT	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72846094	ATAGATAGATAGATA[-/GAA/GAT]AGTAGTTACGATTAC	9873
rs10664954	in-del	-/CAAA	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72880087	AAACAAACAAACAAA[-/CAAA]AACCACCCAAAAAAC	9873
rs10670606	in-del	-/AAA			intron-variant	FCHSD2	GRCh38.p7	11:72968105	AAAAAAAAAAAAAAA[-/AAA]GAAGTGGGCAGAGAA	9873
rs10674308	in-del	-/AA/AAA	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72899758	AAAAAAAAAAAAAAA[-/AA/AAA]GACTTTTTAAATGAT	9873
rs10688506	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:72962601	CCCCCTTTTTTTTTT[-/T]AAACTAAGAATGTTC	9873
rs10732893	snp	C/T	0.0872718	0.189788	intron-variant	FCHSD2	GRCh38.p7	11:72905205	GCTTGTAGTTGGCCA[C/T]CTTCTTCTGGTATCT	9873
rs10736787	snp	C/T	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:72863028	TCTGGGTTCAAGATA[C/T]CTTCTTGCTTTAGCC	9873
rs10736788	snp	A/G	0.101301	0.200969	intron-variant	FCHSD2	GRCh38.p7	11:72900963	TAATAATGCCAATGC[A/G]TGCCTTCTCATTTTG	9873
rs10736789	snp	A/C	0.0178098	0.0926698	intron-variant	FCHSD2	GRCh38.p7	11:72901660	tggttaaaaatggta[A/C]tttttgtgttatgtg	9873
rs10736790	snp	A/G	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:72934549	ATGTTGGCCAGGCTG[A/G]TCTCAAACTCCTGAC	9873
rs10736791	snp	A/G	0.0879971	0.190408	intron-variant	FCHSD2	GRCh38.p7	11:72969074	TCAATTTAAAATAGT[A/G]TACCTGGGGTATCAC	9873
rs10751217	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72856912	CATATTCTAGGAAAG[G/T]TTACAGGCATTTAAA	9873
rs10751218	snp	C/G	0.00279162	0.0372561	intron-variant	FCHSD2	GRCh38.p7	11:72857166	CAGTGCCAGCAATAG[C/G]GGTCACTGTCATATG	9873
rs10751219	snp	C/T	0.102014	0.201495	intron-variant	FCHSD2	GRCh38.p7	11:72857193	TATGCTTCTGCATTG[C/T]TCTAGCTGCTTTCCA	9873
rs10751220	snp	A/T	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:72863261	AATGATGCAAAGGCA[A/T]TTCAGTGGCGAAAGG	9873
rs10751221	snp	C/G	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:72891207	AAAGTGTTCAAATTA[C/G]AGGGATGAGCCAGTA	9873
rs10751223	snp	C/T	0.0178098	0.0926698	intron-variant	FCHSD2	GRCh38.p7	11:72917135	GACTACAGGCACCCA[C/T]CACCACGCCCAGCCA	9873
rs10751224	snp	A/G	0.0182019	0.0936463	intron-variant	FCHSD2	GRCh38.p7	11:72917176	TTTTAGTAGAGATGA[A/G]GTTTCACCATATTGG	9873
rs10793048	snp	C/T	0.443195	0.158668	intron-variant	FCHSD2	GRCh38.p7	11:72869353	CTTCCCTGGCACAGA[C/T]GCTAATTTTTCACTT	9873
rs10793049	snp	C/T	0.49975	0.0111793	intron-variant	FCHSD2	GRCh38.p7	11:72883195	AAATGTTTAGGACCA[C/T]AGTCCACAAAGAAAA	9873
rs10793052	snp	A/G	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72910338	CTCCGAAGAGACAGC[A/G]ACCATCGAGAACGGG	9873
rs10793054	snp	A/C	0.483923	0.0882034	intron-variant	FCHSD2	GRCh38.p7	11:72951767	AATCTGTTATTTTCC[A/C]ATTGATTTGAGGTTT	9873
rs10793055	snp	C/T	0.489434	0.0719116	intron-variant	FCHSD2	GRCh38.p7	11:72999716	GGTAGTTAAACTCTC[C/T]AAATATTCTGATATT	9873
rs10793056	snp	C/T	0.499923	0.00618962	intron-variant	FCHSD2	GRCh38.p7	11:73049120	GATTTAATAGCAAGA[C/T]ATGTAAAAAGACGTA	9873
rs10898884	snp	A/G	0.418491	0.184691	intron-variant	FCHSD2	GRCh38.p7	11:72848523	TTTCACACTTGTTCT[A/G]TTTTCCAGTTTAATA	9873
rs10898885	snp	C/T	0.442385	0.15965	intron-variant	FCHSD2	GRCh38.p7	11:72860230	CAGGCCATGGACCGG[C/T]AAAAGGTTCGTTCCA	9873
rs10898887	snp	C/T	0.429987	0.173507	intron-variant	FCHSD2	GRCh38.p7	11:72870249	CTAAAGCACTCTATA[C/T]AGATCTAATTACAAT	9873
rs10898888	snp	A/G	0.0581099	0.160244	intron-variant	FCHSD2	GRCh38.p7	11:72881846	taattatagaagtag[A/G]gagtagaGGCTGGgg	9873
rs10898889	snp	C/G	0.301429	0.244653	intron-variant	FCHSD2	GRCh38.p7	11:72894337	ACTGCTTGAGGCCAG[C/G]AGTTTGAGACCAGCC	9873
rs10898890	snp	A/C	0.0532157	0.154195	intron-variant	FCHSD2	GRCh38.p7	11:72913835	AACCCAAAAAAAaaa[A/C]aaaaaaaaaaaccct	9873
rs10898892	snp	G/T	0.0984431	0.198823	intron-variant	FCHSD2	GRCh38.p7	11:72949745	tattccactgtatgg[G/T]tttaccacatcttgt	9873
rs10898893	snp	C/T	0.398354	0.201224	intron-variant	FCHSD2	GRCh38.p7	11:72965654	CTTGGGTAATTACCA[C/T]CCAGATCAAGATTTA	9873
rs10898894	snp	C/T	0.498714	0.0253268	intron-variant	FCHSD2	GRCh38.p7	11:72989734	ACTCTTATAACACAC[C/T]GGGGCCAAGCAACAC	9873
rs10898895	snp	A/T	0.479583	0.0989539	intron-variant	FCHSD2	GRCh38.p7	11:73030353	ATGCAATAGAGAGAT[A/T]ATACTAAATAAAAAA	9873
rs10898896	snp	C/T	0.499937	0.0055907	intron-variant	FCHSD2	GRCh38.p7	11:73080844	AGCTACTCAGGAAGC[C/T]GAGGCAGGAGAATCA	9873
rs10898897	snp	A/G	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73113553	TCTCTATTTTTAGTA[A/G]AAACGGGGTTTCGCC	9873
rs10898898	snp	A/G	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73113627	TGTCCAGGCATTGAA[A/G]AGTTTGGTATTTATT	9873
rs10898899	snp	A/G	0.00848641	0.0645847	intron-variant	FCHSD2	GRCh38.p7	11:73113760	TGTCAGGTATCTGAA[A/G]AAACTTGGGTGTTGT	9873
rs10898900	snp	A/T	0.499087	0.0213463	intron-variant	FCHSD2	GRCh38.p7	11:73133347	ATTATTAATAATAGT[A/T]AAAAGTAGAAACAAC	9873
rs10898901	snp	G/T	0.00597247	0.0543191	intron-variant	FCHSD2	GRCh38.p7	11:73137026	gagcgagactttgtc[G/T]caaaaacaaacaaaa	9873
rs11235607	snp	A/G	0.0142736	0.0832652	intron-variant	FCHSD2	GRCh38.p7	11:72845377	agggaggcagaggtt[A/G]cagtgagccgagatc	9873
rs11235608	snp	C/G	0.097727	0.198275	intron-variant	FCHSD2	GRCh38.p7	11:72861643	ATCAATATATAGAAA[C/G]GATAGGCCGGGCGCG	9873
rs11235609	snp	A/G	0.00557542	0.0525036	intron-variant	FCHSD2	GRCh38.p7	11:72873188	caaaaaattagccgg[A/G]cacggtggcgggtgc	9873
rs11235610	snp	C/T	0.00755907	0.0610114	intron-variant	FCHSD2	GRCh38.p7	11:72884997	TTTTGTATAGGTATT[C/T]ATAATAAATAAAGTA	9873
rs11235611	snp	C/G	0.227664	0.249	intron-variant	FCHSD2	GRCh38.p7	11:72898960	gtgttgcccaggctg[C/G]tctcgaactcctggg	9873
rs11235612	snp	A/G	0.481087	0.0953875	intron-variant	FCHSD2	GRCh38.p7	11:72902228	GGTACAACATAAAAA[A/G]TTTCAGGGAAAATAT	9873
rs11235613	snp	A/C	0.0532157	0.154195	intron-variant	FCHSD2	GRCh38.p7	11:72913834	AAACCCAAAAAAAAA[A/C]caaaaaaaaaaaccc	9873
rs11235614	snp	G/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72917201	TATTGGCCAGGCTGG[G/T]CTTGAACTCCTGATC	9873
rs11235617	snp	C/T	0.281577	0.247998	intron-variant	FCHSD2	GRCh38.p7	11:72933586	ATGATACCCAACTTA[C/T]ATTAGCCATATCCAA	9873
rs11235618	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72949241	GATCACCTGAGGTCA[A/G]GAGTTCAAGGCCAGC	9873
rs11235619	snp	A/G	0.00734384	0.0601497	intron-variant	FCHSD2	GRCh38.p7	11:72959886	tgtgtgtgtgtgtgt[A/G]tgtgtgATATCAATA	9873
rs11235620	snp	A/T	0.295343	0.245854	intron-variant	FCHSD2	GRCh38.p7	11:72969886	AAATACACACAAGTG[A/T]GACCTGACCCTCATT	9873
rs11235621	snp	C/T	0.00762378	0.061268	intron-variant	FCHSD2	GRCh38.p7	11:72971443	AAGGGAGATTATCTG[C/T]GATTACCTAATCACA	9873
rs11235622	snp	C/T	0.0414363	0.137845	intron-variant	FCHSD2	GRCh38.p7	11:72975708	TTGATCAAAAAAAGT[C/T]TGCAAAAGATAAGTC	9873
rs11235623	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72981000	CTTAACATTAATTCA[C/G]AAAAACAGATATTTT	9873
rs11235624	snp	C/G	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72981226	CTCTATTTTTAATCA[C/G]TTTAGTACCCCACAA	9873
rs11235625	snp	C/G	0.278399	0.248382	intron-variant	FCHSD2	GRCh38.p7	11:72982154	GGGATTTCAGGCAGT[C/G]AACAAAAAGGAAAGA	9873
rs11235626	snp	A/G	0.0554779	0.157039	intron-variant	FCHSD2	GRCh38.p7	11:72983304	gtctcaaaaaaaaaa[A/G]aaaataaataaaaga	9873
rs11235627	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72995080	tggaatcaaataata[A/T]gtggccttatgtttc	9873
rs11235628	snp	C/T	0.27893	0.24832	intron-variant	FCHSD2	GRCh38.p7	11:73002403	AAAGCACTGATGAAG[C/T]TAAGAGCAGCAAAAC	9873
rs11235629	snp	A/G	0.0142736	0.0832652	intron-variant	FCHSD2	GRCh38.p7	11:73009641	ATTTACTTCTCCTTC[A/G]TTTATGAAGGATAAT	9873
rs11235630	snp	C/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73013959	GCAAGCAATCTTCTT[C/T]TTAGGCTGATTTCCT	9873
rs11235631	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73014188	ccaggctggagggta[A/G]tggtgcattcatagc	9873
rs11235632	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73014250	gatcgtcctgcctta[A/G]cctcctgagtagctg	9873
rs11235633	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73014274	gtagctgggactaca[C/T]gcacgtaccaccaca	9873
rs11235634	snp	A/G	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73014414	gattacaggcatgaA[A/G]AAAATCTATTAATAT	9873
rs11235635	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73015717	AGGAAAGAAGTAATT[C/T]TTTTAAAAACTAGAG	9873
rs11235636	snp	C/T	0.279991	0.248195	intron-variant	FCHSD2	GRCh38.p7	11:73021896	GCAACACAAGGAGAC[C/T]CCTGTCTCTGTAAAT	9873
rs11235637	snp	C/T	0.0058139	0.0536018	intron-variant	FCHSD2	GRCh38.p7	11:73024207	ACCGAAGATAGAATG[C/T]AGACTGTGACAAATC	9873
rs11235638	snp	C/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73031741	CCCGTTATTCTATTT[C/T]TCACCATTGATATGA	9873
rs11235639	snp	C/T	0.404035	0.196909	intron-variant	FCHSD2	GRCh38.p7	11:73033785	AATTAGTTATGAGTA[C/T]TCTTGGATAAGACAC	9873
rs11235640	snp	A/G	0.281577	0.247998	intron-variant	FCHSD2	GRCh38.p7	11:73039293	gaagcagaggtgggc[A/G]gatcacttgaggtca	9873
rs11235641	snp	A/G	0.330947	0.236533	intron-variant	FCHSD2	GRCh38.p7	11:73044721	TATATAGAAAACAGT[A/G]CACATAGTACATGCA	9873
rs11235642	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73049547	ggtggggtcggggga[A/G]gggggagggatagca	9873
rs11235643	snp	A/G	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73049787	GGGCTACCATTTTTA[A/G]AGGGTACGTTCTTAC	9873
rs11235644	snp	C/G	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73049971	AGAAACTAACTATAA[C/G]CTGAATGCTTTGAGA	9873
rs11235645	snp	C/T	0.0414363	0.137845	intron-variant	FCHSD2	GRCh38.p7	11:73053229	GTTGAAAAATTATCA[C/T]TAACCTTACAAATTT	9873
rs11235646	snp	G/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73067412	TGCAACAAACCACCA[G/T]GGCACATTACACCTA	9873
rs11235647	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73071535	tttctactaaaaata[A/C]aaaaaaaaaaaaaaa	9873
rs11235648	snp	C/T	0.0429648	0.14013	intron-variant	FCHSD2	GRCh38.p7	11:73071840	ATCCCTCAAAGGTTA[C/T]AGGGAAAACATAAAT	9873
rs11235650	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73082210	ggcgtgatggcgtgt[C/G]cctgtcatcccagct	9873
rs11235651	snp	A/G	0.498964	0.02274	intron-variant	FCHSD2	GRCh38.p7	11:73090468	CTGACCTCGTGATCC[A/G]CCCGCCTCGGCCTCC	9873
rs11235652	snp	A/G	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73092977	aatgtgatttcatca[A/G]gggtgggtgggatga	9873
rs11235653	snp	A/G	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73093011	gccttgggtcactca[A/G]tatcatctcaacctc	9873
rs11235654	snp	A/G	0.363985	0.222503	intron-variant	FCHSD2	GRCh38.p7	11:73094817	AGGTATTATTACAGT[A/G]AATACTGCAATAGCA	9873
rs11235655	snp	C/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73099346	AACCCTCATGCATTG[C/T]TGGTGAGAACATAAA	9873
rs11235656	snp	G/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73101583	GCTGGGGCTACAGAT[G/T]CACATACCATGCCCA	9873
rs11235659	snp	A/G	0.0425829	0.139564	intron-variant	FCHSD2	GRCh38.p7	11:73105508	AATAGAGAAGAAATC[A/G]TAAGATCTAAATCTT	9873
rs11235661	snp	A/G	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73113413	TCACTCTGTCACCTA[A/G]ATTGGAGTGCAGTGA	9873
rs11235662	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73114588	CCCAAGACCCACAGC[A/G]TACTAACTAGGTATT	9873
rs11235663	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73126173	ggtgaaatcccatct[C/T]tactaaaaatacaaa	9873
rs11235664	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73126337	agggcaagattccat[C/T]ttaaaaaaaaaaaaa	9873
rs11235665	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73133458	AATGAAGTAATGATA[C/T]TACAACCTGATGAAT	9873
rs11274372	in-del	-/ATGCTCA	0.0113471	0.0744635	intron-variant	FCHSD2	GRCh38.p7	11:72947756	AAACATAATTTTCTC[-/ATGCTCA]ATAAAGAAAATTAAA	9873
rs11289761	in-del	-/T	0.397452	0.201886	intron-variant	FCHSD2	GRCh38.p7	11:73045989	CAATAATTTCAGTAA[-/T]TTTTTTTTTTTTTTT	9873
rs11299720	in-del	-/A	0.447291	0.153545	intron-variant	FCHSD2	GRCh38.p7	11:73055344	TGAGACCCTGTCTCG[-/A]AAAAAAAAAAAAATT	9873
rs11358083	in-del	-/G	0.0182019	0.0936463	intron-variant	FCHSD2	GRCh38.p7	11:72871605	CAAGTTGGAGCTGGT[-/G]CAGTGGCTTGTACCT	9873
rs11400132	in-del	-/T	0.113685	0.209567	intron-variant	FCHSD2	GRCh38.p7	11:72948671	TTCTTTTTTTTTTTT[-/T]GAGAGGCAGTCTCGC	9873
rs11403113	in-del	-/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72948683	TTCTTTTTTTTTTTT[-/T]GAGAGGCAGTCTCGC	9873
rs11408216	in-del	-/TTT	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72959237	TTTTTTTTTTTTTTT[-/TTT]GAGACGGAGTCTCGC	9873
rs11561004	snp	A/G	0.375	0.216506	intron-variant	FCHSD2	GRCh38.p7	11:73113389	TTTTTTTTTTTCTGA[A/G]ACAAGGTCTCACTCT	9873
rs11600265	snp	G/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73103522	CAAAGCACATATCTG[G/T]CTTATTGCTAACTAT	9873
rs11600585	snp	A/G	0.19646	0.2442	intron-variant	FCHSD2	GRCh38.p7	11:73016795	AATAAACTGTTTTAC[A/G]AAGAAATTTGCCCAC	9873
rs11601531	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73080074	gaggctgagacagga[A/G]aattacttgaaccca	9873
rs11602688	snp	C/T	0.488965	0.0734569	intron-variant	FCHSD2	GRCh38.p7	11:72888711	gtaacctccacctcc[C/T]gggctcaagcaattc	9873
rs11602858	snp	C/G	0.225893	0.248835	intron-variant	FCHSD2	GRCh38.p7	11:72904024	TTTATAATCTGGGAA[C/G]TGGGCGAACCAAACA	9873
rs11603032	snp	C/T	0.375	0.216506	intron-variant	FCHSD2	GRCh38.p7	11:73113365	ggtcttttttttttt[C/T]ttttttttttttttt	9873
rs11603313	snp	A/G	0.242488	0.249887	intron-variant	FCHSD2	GRCh38.p7	11:72877132	GCTGGGACTACAGGC[A/G]TGCACCACCATGCCC	9873
rs11603605	snp	C/T	0.00716266	0.059414	intron-variant	FCHSD2	GRCh38.p7	11:73061713	gaagttcgaactggg[C/T]ggagcccactgcagc	9873
rs11603656	snp	A/G	0.00397613	0.0444101	intron-variant	FCHSD2	GRCh38.p7	11:72923652	ctcatttttaaatta[A/G]gttgtcaggttgggt	9873
rs11604494	snp	C/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72942524	ATATGTAATACATGC[C/T]TAGGAAAGATTAGAA	9873
rs11604996	snp	A/G	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:73031269	gattgctagagccaa[A/G]tttgagaccagcctg	9873
rs11605166	snp	C/T	0.237882	0.249706	intron-variant	FCHSD2	GRCh38.p7	11:72958732	AAGTTTTATCTATAG[C/T]CACTTAAAAGTAATC	9873
rs11606064	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73045034	gagatcgctccactg[C/G]actccagcctgggcg	9873
rs11607217	snp	G/T	0.0115144	0.0749975	intron-variant	FCHSD2	GRCh38.p7	11:72937040	tttaaataGCAGATT[G/T]CTGCTCATCAACCCT	9873
rs11607724	snp	C/T	0.0286	0.116112	intron-variant	FCHSD2	GRCh38.p7	11:73083649	TCTGTCCTTAAGCCA[C/T]GGAAAAGAAGTATAC	9873
rs11607937	snp	C/G	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73048849	AATCTACCATAAACT[C/G]TAAGAAAAATTCCCA	9873
rs11820561	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73126273	tgaacctgggaggca[A/G]aggttgcagtgagct	9873
rs11821121	snp	C/T	0.00755907	0.0610114	intron-variant	FCHSD2	GRCh38.p7	11:72901267	ccaggcacagtggtg[C/T]gtgcctgtggcccca	9873
rs11821583	snp	C/T	0.00399732	0.0445273	intron-variant	FCHSD2	GRCh38.p7	11:73077641	caacaggaaaatgga[C/T]aaactgtggtatatc	9873
rs11822039	snp	A/C	0.349233	0.229462	intron-variant	FCHSD2	GRCh38.p7	11:72927659	TGCATTTTCTAACAA[A/C]TTGCCACTGGCCTGG	9873
rs11822262	snp	C/T	0.0482946	0.147699	intron-variant	FCHSD2	GRCh38.p7	11:73033471	AATCTCTAAGGTCTC[C/T]GCTTATAAACATACT	9873
rs11822441	snp	C/T	0.0444908	0.142359	intron-variant	FCHSD2	GRCh38.p7	11:73028252	gcagagccacaagga[C/T]agagatgcttaaggc	9873
rs11822832	snp	A/G	0.0154538	0.0865337	intron-variant	FCHSD2	GRCh38.p7	11:72851729	gcctggtgacagagc[A/G]agactctgtctcaaa	9873
rs11823266	snp	C/T	0.0142736	0.0832652	intron-variant	FCHSD2	GRCh38.p7	11:72929190	ataaacatacgtgtg[C/T]gtgtgtctttatagc	9873
rs11823409	snp	C/T	0.0146672	0.084371	intron-variant	FCHSD2	GRCh38.p7	11:72889102	tgggactacaggtgc[C/T]cgccaccacactcgg	9873
rs11824657	snp	C/T	0.0829062	0.185956	intron-variant	FCHSD2	GRCh38.p7	11:73042208	gggactacaggcatg[C/T]gccactgcacccggc	9873
rs11825680	snp	A/T	0.0150606	0.0854603	intron-variant	FCHSD2	GRCh38.p7	11:72928909	cccgatgtgtgatgt[A/T]ccccttcctgtgtcc	9873
rs11826158	snp	A/G	0.0138799	0.0821421	intron-variant	FCHSD2	GRCh38.p7	11:73002407	CACTGATGAAGTTAA[A/G]AGCAGCAAAACGAAT	9873
rs11826537	snp	C/T	0.0146672	0.084371	intron-variant	FCHSD2	GRCh38.p7	11:73118262	aggcagagactgcgg[C/T]gagccgagactgtgc	9873
rs11827636	snp	A/T	0.0209421	0.100162	intron-variant	FCHSD2	GRCh38.p7	11:73131721	aaaaaaaaaaaaatt[A/T]aaaaatttaaaaaat	9873
rs11828012	snp	A/T	0.0138799	0.0821421	intron-variant	FCHSD2	GRCh38.p7	11:73131001	TTGAAAGAATACTAA[A/T]TGAGAAGCAACTATG	9873
rs11828852	snp	C/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:72883542	acttataaaaagatg[C/T]tcagcatagttagtt	9873
rs11828873	snp	A/G	0.0138799	0.0821421	intron-variant	FCHSD2	GRCh38.p7	11:72990419	tcttctcagcaccac[A/G]ctgcacttattccaa	9873
rs12099370	snp	A/T	0.0494327	0.149241	intron-variant	FCHSD2	GRCh38.p7	11:72967952	aaaaattagccgggt[A/T]tggtggcgggcacct	9873
rs12225691	snp	A/C	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72845462	AAAAAAAAAAAAAAA[A/C]AACAACAAACAAACA	9873
rs12226295	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72913833	AAAACCCAAAAAAAA[A/C]Acaaaaaaaaaaacc	9873
rs12226301	snp	A/G	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72910206	tgggaggtgaggagc[A/G]cctctgcctggctgc	9873
rs12269846	snp	A/G	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72980677	TATGTGTGTGTGTGT[A/G]TATATATATATATAT	9873
rs12271446	snp	A/G	0.0142736	0.0832652	intron-variant	FCHSD2	GRCh38.p7	11:72967874	aggcgggcggatcac[A/G]aggtcaggagattga	9873
rs12272713	snp	G/T	0.0146672	0.084371	intron-variant	FCHSD2	GRCh38.p7	11:72991719	tcaacaacgcttcat[G/T]ctaaaaactctcaat	9873
rs12273962	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73097234	gtcttaaacttctga[A/G]ctcaagctatccacc	9873
rs12277770	snp	C/T	0.0142736	0.0832652	intron-variant	FCHSD2	GRCh38.p7	11:72863061	ctgagtagctaggac[C/T]gcaggaatgtaccac	9873
rs12278657	snp	C/T	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:72924316	agagtcttgctctat[C/T]gcccaggctggagtg	9873
rs12279812	snp	C/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72929422	ACATGAACTCATTTT[C/T]TGGTGGGTAAGATAG	9873
rs12279856	snp	C/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72929449	ATAGCTGGAGGCCTT[C/T]TGGCCTGGGTGGATT	9873
rs12283235	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72954336	aactcagcctcctga[A/G]tagctgggaccacag	9873
rs12283244	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72954393	attttattttttgta[A/G]agatggggtctcaca	9873
rs12283360	snp	C/G	0.0146672	0.084371	intron-variant	FCHSD2	GRCh38.p7	11:72924520	atctcctgatctcgt[C/G]atccgcccaccttgg	9873
rs12288050	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72914355	gctattcccattgaa[A/C]taccattgacattct	9873
rs12288464	snp	A/G	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73027727	atcacaggcccagga[A/G]gcctaggaaggaaaa	9873
rs12288580	snp	A/G	0.499477	0.0161657	intron-variant	FCHSD2	GRCh38.p7	11:72997843	gtagctgggactgca[A/G]gcatgaaccaccaca	9873
rs12289752	snp	C/T	0.499693	0.0123764	intron-variant	FCHSD2	GRCh38.p7	11:72850093	TTTGAGATGGAATTT[C/T]GCTCTTGTCACCCCG	9873
rs12290337	snp	A/G	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73130776	CCAACATAACTGACC[A/G]TAATATGGAAGTATA	9873
rs12291530	snp	C/G	0.0146672	0.084371	intron-variant	FCHSD2	GRCh38.p7	11:73099688	GCTTAGCGGCGCTCA[C/G]CACCCTGGTTCTTCT	9873
rs12293726	snp	C/T	0.499741	0.0113788	intron-variant	FCHSD2	GRCh38.p7	11:72882713	aaaggaaaCAGAGTG[C/T]ctaaataaatagaga	9873
rs12294037	snp	A/T	0.326035	0.238157	intron-variant	FCHSD2	GRCh38.p7	11:73096586	ggaTGAAAGAAAGCA[A/T]ATACCACTTCCAGAT	9873
rs12294101	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73053063	gttggccagactagt[C/T]tcaaactcctggcct	9873
rs12294533	snp	C/T	0.49925	0.0193545	intron-variant	FCHSD2	GRCh38.p7	11:72973853	acatagccacattca[C/T]GGCTGCACTGCAACA	9873
rs12295119	snp	A/G	0.0138799	0.0821421	intron-variant	FCHSD2	GRCh38.p7	11:73094906	AACAACTGAAGCTAT[A/G]TTGTAAGTCTGGCAG	9873
rs12295496	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72911761	cgcttttgttgccta[A/G]gctggagtgcactgg	9873
rs12361657	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72892617	ttgttttgttttttg[G/T]tttttgagacagagt	9873
rs12362045	snp	A/G	0.281313	0.248031	intron-variant	FCHSD2	GRCh38.p7	11:73107418	acatgagatattttg[A/G]tacaggcatgcaatg	9873
rs12362488	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72933942	agcaagactccatct[C/T]tacaaagaatacaaa	9873
rs12362637	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72892616	tttgttttgtttttt[G/T]ttttttgagacagag	9873
rs12364310	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73132656	ggcaaaaccccatct[C/T]tacaaaaaaatacaa	9873
rs12364319	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73132798	cccctgcactccagt[C/T]tgggtgacagaatga	9873
rs12364876	snp	A/G	0.00874735	0.0655527	intron-variant	FCHSD2	GRCh38.p7	11:72871365	CTTTGTTCAGAGTCA[A/G]TGTGTTTTGTGTCAT	9873
rs12365275	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73099641	gtaaaacactgatac[C/T]GCCCAGGCACCCCTG	9873
rs12417882	snp	A/C	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72983728	CAATAATTTATTGAA[A/C]CCATGACATGAGTCT	9873
rs12418389	snp	C/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73024308	ttctgtaaaataatg[C/T]gtttataaatggatt	9873
rs12418398	snp	G/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73024405	aacattgtacactag[G/T]tgataaagttgtttc	9873
rs12418521	snp	C/T	0.00571424	0.0531457	intron-variant	FCHSD2	GRCh38.p7	11:73117189	acatattaacttatt[C/T]aatcttcacaaacct	9873
rs12418733	snp	A/T	0.143284	0.226079	intron-variant	FCHSD2	GRCh38.p7	11:72959970	TTAAAAGCACAGATA[A/T]ATAGGAAGAAACCTA	9873
rs12418930	snp	C/T	0.332106	0.236133	intron-variant	FCHSD2	GRCh38.p7	11:72970521	TTTTAGAATTCTTTC[C/T]TCAAGGTCAAATTTT	9873
rs12419074	snp	A/C	0.0517044	0.152246	intron-variant	FCHSD2	GRCh38.p7	11:72905483	tagggtacataggca[A/C]aacgtgcaggtttgt	9873
rs12419767	snp	A/T	0.0445173	0.142534	intron-variant	FCHSD2	GRCh38.p7	11:72887065	ATGGGGGAGATTTCC[A/T]AAGCTCTGAAAATAT	9873
rs12419915	snp	G/T	0.318174	0.240525	intron-variant	FCHSD2	GRCh38.p7	11:73116716	AATTGCTTTTTATTT[G/T]TATTAGGGACAGGAT	9873
rs12421091	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73021499	acttataaatgggag[A/C]taaatgatgagaaca	9873
rs12421489	snp	A/C	0.0364509	0.129988	intron-variant	FCHSD2	GRCh38.p7	11:73038099	ATCTATCACTAAAAA[A/C]TTCTTATGAcgaggt	9873
rs12421713	snp	A/G	0.444444	0.157135	intron-variant	FCHSD2	GRCh38.p7	11:72910861	AAAAtttcctataga[A/G]ttgtttgagctcctt	9873
rs12421979	snp	A/C	0.00938946	0.0678717	intron-variant	FCHSD2	GRCh38.p7	11:73069887	CAAAGAATCTAAATC[A/C]CTTATCAGATTATAT	9873
rs12574340	snp	C/G	0.00961516	0.0686668	intron-variant	FCHSD2	GRCh38.p7	11:73038902	ATCCATATAAATTAT[C/G]ACATGCCTCCCACTT	9873
rs12577122	snp	G/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73028374	ccctgttacgtttca[G/T]acttgcatggggcct	9873
rs12786299	snp	C/T	0.0611083	0.163768	intron-variant	FCHSD2	GRCh38.p7	11:72994581	TATAGTGTAAACTca[C/T]ggtgaaaccccgtct	9873
rs12787405	snp	C/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73115768	aggcaaaatttcttc[C/T]tcttccagatacctc	9873
rs12788845	snp	A/T	0.0618563	0.164627	intron-variant	FCHSD2	GRCh38.p7	11:73049651	TAACTAACCTGCACA[A/T]TGTGCACATGTACCC	9873
rs12790346	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72949333	tgggtgcctgtaatc[A/T]cagctactcaggagg	9873
rs12792581	snp	G/T	0.00991711	0.0697152	intron-variant	FCHSD2	GRCh38.p7	11:72887764	ACTACAGACAGTCCC[G/T]TCAGTGGGGAAGCCA	9873
rs12793115	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72858510	tccttagcaaactaa[C/T]acaggaacagaagac	9873
rs12793125	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72858518	aaactaacacaggaa[A/C]agaagaccaaatacc	9873
rs12793835	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72858511	ccttagcaaactaac[A/G]caggaacagaagacc	9873
rs12793874	snp	C/T	0.0490535	0.14873	intron-variant	FCHSD2	GRCh38.p7	11:73110024	aaccatccttgcatc[C/T]ctgggatatatctca	9873
rs12795254	snp	A/G	0.0117874	0.0758601	intron-variant	FCHSD2	GRCh38.p7	11:72958965	TTCGGCACTCCTACA[A/G]GATATTACATATACT	9873
rs12796371	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73096376	tgaaaccctgcctct[A/C]caaaaaaaaaaaaaa	9873
rs12796487	snp	A/G	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73082362	aaaaaaaaaaaaaaa[A/G]gaaAAGAAAAAGCAT	9873
rs12799184	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72858499	ggaggccattatcct[C/T]agcaaactaacacag	9873
rs12799199	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72976972	gctctgttgcccagg[A/C]tggagtgcagtggca	9873
rs12799445	snp	G/T	0.383439	0.21141	intron-variant	FCHSD2	GRCh38.p7	11:72881461	aaattagtacagcta[G/T]tatggaaaacagcat	9873
rs12801447	snp	C/T	0.00517822	0.0506191	intron-variant	FCHSD2	GRCh38.p7	11:73089506	cagcagcattattca[C/T]aatatccaaacagta	9873
rs12803589	snp	A/C	0.0629771	0.165899	intron-variant	FCHSD2	GRCh38.p7	11:72856122	TACATTAATTAATTA[A/C]AGTATCAAATATCTA	9873
rs12803782	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73097664	atcccttcacttgtt[A/G]ttgagaatttctatt	9873
rs12805492	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:73115770	gcaaaatttcttctt[C/G]ttccagatacctcag	9873
rs12805658	snp	A/C	0.296873	0.245566	intron-variant	FCHSD2	GRCh38.p7	11:72844255	CCATGGACAAGCATG[A/C]AGTGAAAATGCAAAG	9873
rs12807905	snp	A/G	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73084435	ttgttctgttgccta[A/G]gcttgagtgcggcgg	9873
rs12808211	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73090220	TAATTACAATACttc[C/T]ttttttttttttttt	9873
rs12808472	snp	G/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73097540	ttttagtaggattgg[G/T]gttaattcatcatta	9873
rs12808516	snp	C/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73097604	agtcctattatttct[C/T]gtgaggtgttctttt	9873
rs12808517	snp	C/T	0.167809	0.236103	intron-variant	FCHSD2	GRCh38.p7	11:72890231	ATGGACTTATCTTTC[C/T]GAGTGGGAAGGAAGC	9873
rs12808532	snp	C/T	0.0246875	0.108325	splice-acceptor-variant, intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840960	CATGAAGGCTTTTTT[C/T]TAAGGGAGAAAACCA	9873
rs17131809	snp	C/G	0.00891185	0.0661552	intron-variant	FCHSD2	GRCh38.p7	11:72984069	AGTAAAATTACCATA[C/G]ATATGAAAGCTGTAT	9873
rs17131810	snp	C/T	0.0228947	0.104514	intron-variant	FCHSD2	GRCh38.p7	11:72988541	AGTGCTTTTGTTCAC[C/T]TGATGTGTTCATGGA	9873
rs17131814	snp	C/T	0.0119091	0.0762411	intron-variant	FCHSD2	GRCh38.p7	11:73009116	TAATGACATTAAATG[C/T]TGCATGTATCATCAG	9873
rs17131835	snp	C/T	0.0225045	0.103662	intron-variant	FCHSD2	GRCh38.p7	11:73117926	ATTTGCTTATCTTTT[C/T]ATGTAAAACTACTTA	9873
rs17131839	snp	C/T	0.144296	0.226554	intron-variant	FCHSD2	GRCh38.p7	11:73119451	AGGTGTGTTAAAATC[C/T]CCTACTATGATGACA	9873
rs17244499	snp	A/G	0.213333	0.247296	intron-variant	FCHSD2	GRCh38.p7	11:72918901	AATACCTATGACAAC[A/G]TCTGCTTCAGTTACA	9873
rs17310235	snp	A/G	0.279461	0.248258	intron-variant	FCHSD2	GRCh38.p7	11:72896031	AAATTTTTGCCAAAT[A/G]TTTTTTTAATAGATG	9873
rs17310277	snp	C/G	0.0501905	0.150254	intron-variant	FCHSD2	GRCh38.p7	11:73050365	AATAAGTGAAAAAGA[C/G]GTATTTAGATTGATA	9873
rs28576960	snp	C/G	0.00717793	0.0594764	intron-variant	FCHSD2	GRCh38.p7	11:72887449	ACCTGGGCAAAATGC[C/G]ACAATTAGCTGCCAC	9873
rs28836317	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73108573	TTTTTGTTTGTTTTT[G/T]GTTTTTGAGACGGAG	9873
rs33927802	in-del	-/A/G			intron-variant	FCHSD2	GRCh38.p7	11:72966206	CTGTCGCCCAGGAAG[-/A/G]AGGAGTGCAGTGGTG	9873
rs34032042	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73120749	AATAATAATAATAAA[A/C]CAAAAATTAAAAAAA	9873
rs34035620	in-del	-/G			intron-variant	FCHSD2	GRCh38.p7	11:72950206	TATTTGTTTTTATTG[-/G]AATTGTAAAGCTTCT	9873
rs34040239	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:72899758	AAAAAAAAAAAAAAA[-/A]GACTTTTTAAATGAT	9873
rs34046234	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:72914500	AACTATACCACAGGG[-/T]CCACAGCAACCAAAC	9873
rs34071391	in-del	-/G			intron-variant	FCHSD2	GRCh38.p7	11:72935856	CAAAACCAGGAAAGG[-/G]AAAATTTCAATGCTG	9873
rs34079336	in-del	-/G			intron-variant	FCHSD2	GRCh38.p7	11:72948747	TCGGCTCACTGCAAG[-/G]CTCCATCTCCCAGGT	9873
rs34104790	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:73138076	TGCAAGCAAAATGTG[-/T]ATGGATCAGCAATAA	9873
rs34132603	in-del	-/G			intron-variant	FCHSD2	GRCh38.p7	11:72961027	GACCTAGGAATGGGG[-/G]AGGTAACACACATGT	9873
rs34145074	in-del	-/C			intron-variant	FCHSD2	GRCh38.p7	11:72961710	CAAAATGCAATGATC[-/C]TCTAAAGATTGCTGT	9873
rs34152540	snp	A/G	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:72983155	AAAAATTAGCTGGGC[A/G]TAGTGGCGGGCGCCT	9873
rs34171649	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72907596	ATTGAGATAATCACG[G/T]GGGTTTTTTTTTTTT	9873
rs34222566	in-del	-/GT			upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73142870	TGTGTGTGTGTGTGT[-/GT]CGGGGGGCGCGGGGG	9873
rs34243814	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73004222	ATTTATCATATCATT[A/T]AATCCTCATCGTAAT	9873
rs34272235	in-del	-/AT			intron-variant	FCHSD2	GRCh38.p7	11:73039929	TATTCATGAGGATAT[-/AT]CACAAAAGCAGTTAT	9873
rs34281399	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:72958071	CCATTTAACTACTTT[-/T]AATGTACTCTGTTGT	9873
rs34289658	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73004234	ATTTAATCCTCATCG[A/T]AATTCTGTAAGATAG	9873
rs34337477	in-del	-/G			intron-variant	FCHSD2	GRCh38.p7	11:73113321	TTCCCTGGTACCTTA[-/G]TTTGGTTGATCATCA	9873
rs34355434	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:72931411	CATGCCCAGCCTTAA[-/A]TTTTTTTTTTAAATA	9873
rs34368733	snp	C/T	0.0333695	0.124785	intron-variant	FCHSD2	GRCh38.p7	11:73051776	TAGTGAATTGCAAAG[C/T]CAACAGAAGCAAATG	9873
rs34375600	in-del	-/C			intron-variant	FCHSD2	GRCh38.p7	11:72996219	TATATTCAAGTTCCC[-/C]ACTCTGTTATTTACT	9873
rs34381314	in-del	-/AC			intron-variant	FCHSD2	GRCh38.p7	11:73121175	TATACACATACACAT[-/AC]ACACACACACACACA	9873
rs34409474	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73113349	TCATGCTTCCCAAGA[A/T]GGTCTTTTTTTTTTT	9873
rs34423603	in-del	-/G			intron-variant	FCHSD2	GRCh38.p7	11:72875660	CATTTTATAGATGAG[-/G]AAAAATGATTTAATC	9873
rs34434620	in-del	-/AG			intron-variant	FCHSD2	GRCh38.p7	11:72908346	TGCAATCAACATGAG[-/AG]TGCAGATATCTCTTT	9873
rs34457446	in-del	-/C			intron-variant	FCHSD2	GRCh38.p7	11:72852915	ATACTGCATGTTCTC[-/C]ACTAATAAGTGGGAG	9873
rs34469455	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:72848433	ATCATGACCTACTTT[-/T]AAATGCCACCTCATC	9873
rs34479848	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:72934248	ATTTAAATGAGCAAA[-/A]CACAAGAATGTTCTT	9873
rs34480047	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:72878792	CTATGAACTGAAAAA[-/A]TTCCTAGAGCTTGTA	9873
rs34484683	in-del	-/A	0.277067	0.24853	intron-variant	FCHSD2	GRCh38.p7	11:72861396	TATTTAAAAACTTCC[-/A]AAAAAAAAAAAAAAC	9873
rs34543987	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:73105842	TTAACCATAATATTT[-/T]GAATCTATTAAGTCT	9873
rs34545128	in-del	-/TT	0.0138799	0.0821421	intron-variant	FCHSD2	GRCh38.p7	11:72982989	AACATAGCAAGACTC[-/TT]GTTTCTAAAAATAAA	9873
rs34545515	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:73109517	CTTTTTCAGATTGTT[-/A]CACTGTTGGCATACA	9873
rs34549459	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:72972584	AGTTTGTTTTAAAAA[-/A]GTTGTTCAACTGCTA	9873
rs34549479	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:72910849	AAAAAAAAAAAAAAA[-/A]TTTCCTATAGAGTTG	9873
rs34568857	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:72986642	CAGTTCTCCTTTTTT[-/T]ACAGTCATTACCCAA	9873
rs34596105	in-del	-/G			intron-variant	FCHSD2	GRCh38.p7	11:72948715	CTGTCGCCCAGGCTG[-/G]AGTGCAGTGGCACAA	9873
rs34606566	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:73027211	ATGGTTTTGACCAAA[-/A]CCATTGATCACTGAT	9873
rs34618970	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:72855326	CAAAAAAGACCAAAA[-/A]GTTGCTGGGTGTGGT	9873
rs34621889	in-del	-/G			intron-variant	FCHSD2	GRCh38.p7	11:73082204	AGCTGGGCGTGATGG[-/G]CGTGTGCCTGTCATC	9873
rs34629501	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:72932407	TTAGGAAAAGGCTTT[-/T]AAAAAAATCATTACA	9873
rs34645477	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72931247	TTACAGGCTTGCACC[A/C]CCAAGCACAAATAAT	9873
rs34649170	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73035082	ACTGGTTAAGAGCAC[A/G]GACACACATTCTCAG	9873
rs34688695	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72931223	GGTCAACCTCCTGAA[A/T]AACTGGGATTACAGG	9873
rs34721324	in-del	-/GT			intron-variant	FCHSD2	GRCh38.p7	11:72924111	GTACAAAAGTTTTAC[-/GT]TTTTTTAAAAAAAGT	9873
rs34730764	in-del	-/G			intron-variant	FCHSD2	GRCh38.p7	11:73094325	CATGCCATTGGTGGG[-/G]AATGTAAAATGGTAC	9873
rs34734980	in-del	-/G			intron-variant	FCHSD2	GRCh38.p7	11:72888151	GAATCTGAGAAACTG[-/G]AATATTTCATTGTGG	9873
rs34760422	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73004245	ATCGTAATTCTGTAA[A/G]ATAGGTATTATTCCC	9873
rs34778607	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:72887315	ACTGCCTTCCACAGA[-/A]GCAGGTACTCAACAA	9873
rs34789461	in-del	-/A			utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72837346	TACTTTTGGTCAAAA[-/A]TCCCATGGGGACATT	9873
rs34801939	in-del	-/C			intron-variant	FCHSD2	GRCh38.p7	11:72894291	GCTCACACTTACAAT[-/C]CCCAGTGTTCTGGTA	9873
rs34802040	in-del	-/A	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73033302	CAAAAAAAAAAAAAA[-/A]GTAGTTAGACTACAG	9873
rs34802367	in-del	-/CG			intron-variant	FCHSD2	GRCh38.p7	11:73029691	GCTGAAGTGACTTCC[-/CG]GGGGAACTTAAAGGG	9873
rs34805873	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:73108055	CTGAGGGTCCCCTTT[-/T]CTCCACATCCTTGCC	9873
rs34809010	snp	C/G	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73065338	TGTGTTCCATCAATA[C/G]CTAATTTATTGAGAG	9873
rs34826105	in-del	-/G			intron-variant	FCHSD2	GRCh38.p7	11:72995675	TGCCACTGCACTCTA[-/G]CAGGGGTGACAGAGC	9873
rs34831733	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:73065322	CTAATTTATTGAGAG[-/T]TTTTAGCATGAAGGG	9873
rs34877807	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:72979038	AATTTTTTGTATTTT[-/T]AGTAGAGATGGATTT	9873
rs34907660	in-del	-/AT	0.0150606	0.0854603	intron-variant	FCHSD2	GRCh38.p7	11:72941221	GGGACCAGAGGCCAC[-/AT]GAGTCTTGTTCACTA	9873
rs34961521	in-del	-/G			intron-variant	FCHSD2	GRCh38.p7	11:73116115	TCTATTTCTAGTTTG[-/G]CTAATAAGAGTTTTT	9873
rs34983470	snp	A/C	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72913825	AACCAAAAAAAACCC[A/C]AAAAAAAAACAAAAA	9873
rs34998210	in-del	-/A	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72883949	AAAAAAAAAAAAAAA[-/A]TTTTTTTTAATGAGG	9873
rs35004484	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:72869851	TCCATCTTTTACAGT[-/A]CTGTGAATGACCTCA	9873
rs35014261	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:72865814	AGAGAAGTGACTTTT[-/T]CCAAGGTGTGCAGAT	9873
rs35023664	in-del	-/C			intron-variant	FCHSD2	GRCh38.p7	11:73128334	CTGGAAATGGGTCCC[-/C]TGCAGCAAATCAGGC	9873
rs35046728	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:72924108	GATGTACAAAAGTTT[-/A]TACTTTTTTAAAAAA	9873
rs35070702	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73124352	TAATATGGCACATGT[A/G]TACATATATAACAAA	9873
rs35072169	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72931202	CGGGTTCAACTGATT[C/T]TCCTGGGTCAACCTC	9873
rs35073299	in-del	-/C			intron-variant	FCHSD2	GRCh38.p7	11:72894891	CACAGGTGCTTCCCC[-/C]ATACATTGCTCAGGG	9873
rs35075086	in-del	-/C			intron-variant	FCHSD2	GRCh38.p7	11:73110016	TATGTTGAACCATCC[-/C]TTGCATCCCTGGGAT	9873
rs35079354	in-del	-/G			intron-variant	FCHSD2	GRCh38.p7	11:73099447	AATTCCACCCCAAGG[-/G]TATATACTCGAGAGA	9873
rs35079551	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:72907619	TTTTTTTTTTTTTTT[-/T]CTTGAGACGGAGTCT	9873
rs35094799	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:73085249	TGTTTATTCAAAAAA[-/A]GTCTCCAGTGCATTC	9873
rs35095680	snp	G/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73097310	CCCACTTGGTCGTGG[G/T]GGATAATCCTTTTAA	9873
rs35096374	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72931251	AGGCTTGCACCCCCA[A/T]GCACAAATAATTTTT	9873
rs35097783	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72931258	CACCCCCAAGCACAA[A/C]TAATTTTTTTGGGTT	9873
rs35116516	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:72973972	TAAGTAAAGACCTAG[-/T]AGTGCAAATGAAGGA	9873
rs35118990	in-del	-/T	0.140919	0.224948	intron-variant	FCHSD2	GRCh38.p7	11:72898729	TTGCTTTTCTTTCTA[-/T]TTTTTTTTTTTTTTT	9873
rs35125566	in-del	-/C			intron-variant	FCHSD2	GRCh38.p7	11:73021481	AAATAATATATGTTC[-/C]TCACTTATAAATGGG	9873
rs35132766	in-del	-/C			intron-variant	FCHSD2	GRCh38.p7	11:72990280	AGACACAATGTCAGC[-/C]TGTGTTATTAGGCAA	9873
rs35141012	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:72865104	TCCACAAGGCACTTT[-/T]CAGTTGCACTATTAA	9873
rs35147758	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:73117672	GAAAGCTTCAACAGA[-/A]TTATTGCAAAATTTT	9873
rs35175051	in-del	-/C			intron-variant	FCHSD2	GRCh38.p7	11:72933236	AAATTAGGTCATCCC[-/C]TGGGATAGAGGCTGA	9873
rs35180337	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:72908385	TGATTTCCTTTCTTT[-/T]GGGTGTATACCTAGC	9873
rs35200645	in-del	-/T	0.399073	0.200692	intron-variant	FCHSD2	GRCh38.p7	11:73108552	GATTTTAGATTTAAG[-/T]TTTTTTTTTTGTTTG	9873
rs35241897	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:72985376	AAAAAAAAAAAAAAA[-/A]CTTGACCAAAAAAAA	9873
rs35245866	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:72932287	TTGCCCTGCATCCAA[-/A]CTCTCCCTCTCACCA	9873
rs35247532	in-del	-/G			intron-variant	FCHSD2	GRCh38.p7	11:72990014	AACTTAACCATATGA[-/G]CATACAGGCTAGACT	9873
rs35256045	in-del	-/C			intron-variant	FCHSD2	GRCh38.p7	11:73057327	GAAGCAAAACAGAAG[-/C]TAAAGAATCACAAGG	9873
rs35265426	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72931267	GCACAAATAATTTTT[G/T]TGGGTTTTTTTTTTT	9873
rs35280672	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:72964807	TTTTTTTTTTTTTTT[-/T]GAGATGGAGTCTTGC	9873
rs35295400	in-del	-/T	0.168135	0.236216	intron-variant	FCHSD2	GRCh38.p7	11:72871773	TTTTTTTTTTTTTTT[-/T]AGAGCCAGAGTGGTT	9873
rs35298009	in-del	-/TA			intron-variant	FCHSD2	GRCh38.p7	11:72980676	GTATGTGTGTGTGTG[-/TA]TATATATATATATAT	9873
rs35308563	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73004141	AAAAAAAAAAGGGAT[A/T]TCAAGCATATACGGT	9873
rs35333793	in-del	-/C			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72842134	TAAAGGCTGTTTCCC[-/C]TGTGATGAACTAAGT	9873
rs35355618	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:72854459	GGTTAGAGACAGGGT[-/A]CTCGCTCTGCTGCCC	9873
rs35362137	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:72912000	TTGTATGTTGATTTT[-/T]GTATCCTGCAACTTT	9873
rs35372802	in-del	-/GA	0.00716266	0.059414	intron-variant	FCHSD2	GRCh38.p7	11:72885237	AAGTGGAAACCAAGT[-/GA]GAGATTATTTTATGC	9873
rs35396245	in-del	-/C			intron-variant	FCHSD2	GRCh38.p7	11:72882268	CAACATGGTAAAACC[-/C]TGTCTTTTATTACAA	9873
rs35402140	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:72869444	GGGGGAGGGAAGAAG[-/T]AGAGAGAGAGAGACA	9873
rs35412486	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:73132825	TGAAACGGTAACAGA[-/A]AAAAAAAAAAAAAAA	9873
rs35415377	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72931225	TCAACCTCCTGAAAA[A/G]CTGGGATTACAGGCT	9873
rs35425292	in-del	-/A/G			intron-variant	FCHSD2	GRCh38.p7	11:72966208	TGTCGCCCAGGAAGA[-/A/G]GGAGTGCAGTGGTGC	9873
rs35440732	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:72996276	TTTAGTTTTATCATT[-/T]GTAAAATAATAATAC	9873
rs35445043	in-del	-/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73129892	TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTCGC	9873
rs35446068	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72931196	GCCTCCCGGGTTCAA[C/G]TGATTTTCCTGGGTC	9873
rs35454108	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:72873285	GTGAACCGAGATCGC[-/T]GCCACTGCACTCCAG	9873
rs35454508	in-del	-/G			intron-variant	FCHSD2	GRCh38.p7	11:73090515	AGGCGTGAGCCACCG[-/G]CGCGCGGCCTACAAT	9873
rs35471658	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:73104748	AATTTTTGTATTTTT[-/T]AGTAGAGACGGGGTT	9873
rs35472110	in-del	-/G			intron-variant	FCHSD2	GRCh38.p7	11:72948689	TTTTTTTTTGAGAGG[-/G]CAGTCTCGCTCTGTC	9873
rs35483502	in-del	-/CT			intron-variant	FCHSD2	GRCh38.p7	11:72985693	AGAAAGTCCTGGGAC[-/CT]TCTGCCCTGTATGAT	9873
rs35496888	snp	A/C	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72998761	ATACAGATCAAAGCC[A/C]CAATAAAATATTAAT	9873
rs35499071	in-del	-/T			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840268	ACTCAATACATATTT[-/T]GCTGAATGAATGAAG	9873
rs35532363	in-del	-/C			intron-variant	FCHSD2	GRCh38.p7	11:72881068	CTATGCAGCAAAGGA[-/C]AACAACAGAGTTAAC	9873
rs35549383	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:73117430	ATATTTTGGGTTTTT[-/T]CCTAATTTATTGAGA	9873
rs35619417	in-del	-/A/ATA			intron-variant	FCHSD2	GRCh38.p7	11:73039928	ATATTCATGAGGATA[-/A/ATA]TCACAAAAGCAGTTA	9873
rs35623691	in-del	-/ATTT	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73035739	TTTATTTATTTATTT[-/ATTT]GAGATGGAGTCTCGC	9873
rs35637378	in-del	-/G			intron-variant	FCHSD2	GRCh38.p7	11:73138364	TACAGACAACAGGGG[-/G]AAAAATGGAGACAAA	9873
rs35645976	in-del	-/G			intron-variant	FCHSD2	GRCh38.p7	11:73004138	AAAAAAAAAAAAAGG[-/G]ATATCAAGCATATAC	9873
rs35661348	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:72913840	AAACAAAAAAAAAAA[-/A]CCCTAGAAATACAGC	9873
rs35694513	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73004289	GAAAATTGAGGCTCA[A/G]AAGGTTGTGAAATTT	9873
rs35708688	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:72846198	TTTTTTTTTTTTTTT[-/T]GAGACGGAGTCTCAC	9873
rs35716158	snp	A/G	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73004274	CCATTTTACAGAGGA[A/G]AAAATTGAGGCTCAG	9873
rs35716767	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:72856016	TATTTGGCTGCTTTT[-/T]CCCATATTCAAACAT	9873
rs35727459	in-del	-/C			intron-variant	FCHSD2	GRCh38.p7	11:72983178	GGCGCCTGTAGTCCC[-/C]AGCTACTTGGGAGGC	9873
rs35731919	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:72853541	GCCTCAGCCTCCCAA[-/A]GTAGCTGGGACTACA	9873
rs35732826	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:72923278	TTGTGTACAAGGTTT[-/T]GTTTGAGCACCTGTT	9873
rs35768116	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:73078808	CTGCAGCCTTGAAAT[-/T]CCTGGACTCACGTGA	9873
rs35807934	in-del	-/G			intron-variant	FCHSD2	GRCh38.p7	11:72882167	AGAGCAGAGGCTGGG[-/G]CATGGTGGCTCATGC	9873
rs35809991	in-del	-/TA			intron-variant	FCHSD2	GRCh38.p7	11:72931070	ATATATATATATATA[-/TA]CCTACTATATACCCA	9873
rs35814650	in-del	-/C			intron-variant	FCHSD2	GRCh38.p7	11:73053964	TTCACTTTTATTGTA[-/C]TTTTACAAAAATGTC	9873
rs35842462	in-del	-/G			intron-variant	FCHSD2	GRCh38.p7	11:73015114	TCCCCAAGTGCTGGG[-/G]ATTACAGGCGTAAGC	9873
rs35846965	in-del	-/G			intron-variant	FCHSD2	GRCh38.p7	11:72893533	TTGCCTAGGCCATCT[-/G]CAAACTCCTGGCCTC	9873
rs35848613	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:73124926	TTAGAGCAAGGGAAA[-/A]GCACATTCCATAGAT	9873
rs35870886	in-del	-/AC			intron-variant	FCHSD2	GRCh38.p7	11:72907593	CTATTGAGATAATCA[-/AC]CGTGGGTTTTTTTTT	9873
rs35891768	in-del	-/C			intron-variant	FCHSD2	GRCh38.p7	11:72924324	CTCTATTGCCCAGGC[-/C]TGGAGTGCAGTGGCA	9873
rs35907738	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:73138787	TAATTTTTGTATTTT[-/T]AGTAGAGACAGGGTT	9873
rs35943868	in-del	-/T	0.466308	0.125343	intron-variant	FCHSD2	GRCh38.p7	11:73111464	TATCTTTCTCCATCC[-/T]TTTTTTTTTTTTCAG	9873
rs35950358	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:72856116	GCCATTACATTAATT[-/T]AATTAAAGTATCAAA	9873
rs35950708	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73004242	CTCATCGTAATTCTG[A/T]AAGATAGGTATTATT	9873
rs35950986	in-del	-/G			intron-variant	FCHSD2	GRCh38.p7	11:72989606	AGCACGAAACCTGGG[-/G]TACCACATAACAATT	9873
rs35955797	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:72895422	TGCGTCTAACACTTT[-/T]GAGAACATACCTAGA	9873
rs35979371	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:73113384	TTTTTTTTTTTTTTT[-/T]CTGAGACAAGGTCTC	9873
rs35985525	in-del	-/G			intron-variant	FCHSD2	GRCh38.p7	11:72893587	CCAAAGTGCTGGGAT[-/G]TAGAGGCATGAGCCA	9873
rs35987613	in-del	-/C			intron-variant	FCHSD2	GRCh38.p7	11:73043531	TTTAAAAACTGACCC[-/C]AATGTACACAGTATA	9873
rs36007050	snp	A/G	0.368529	0.220116	intron-variant	FCHSD2	GRCh38.p7	11:73094032	CCTGGCCAACATGGT[A/G]AAACCCCGTCTCTAC	9873
rs36027531	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:73112097	AGTTTTGTACCTTTA[-/A]GATAATTTCTTATTG	9873
rs36079363	in-del	-/G			intron-variant	FCHSD2	GRCh38.p7	11:72977966	GCATATACACCATGG[-/G]AATACTATGCAGTCA	9873
rs36082894	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72879463	AAAAAGAATGAAATG[A/C]CAGAGATGATGGAAT	9873
rs36085500	in-del	-/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72964790	TTTTTTTTTTTTTTT[-/T]GAGATGGAGTCTTGC	9873
rs36087102	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:73074453	ATATCACATACGAAA[-/A]TTTACTTCAGAAAGA	9873
rs36098721	in-del	-/C			intron-variant	FCHSD2	GRCh38.p7	11:73082221	TGTGCCTGTCATCCC[-/C]AGCTACTCAGGAGGC	9873
rs36113290	in-del	-/CCC	0.0178098	0.0926698	intron-variant	FCHSD2	GRCh38.p7	11:72901319	GGAGGATCACTTGAG[-/CCC]AGGAGAGGGGGGCTG	9873
rs36120997	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:72890110	AGAAAGTTACCAGAA[-/A]GAGTAAGATCAGCAT	9873
rs36148418	in-del	-/C			intron-variant	FCHSD2	GRCh38.p7	11:72938082	GGGAAATACATCCCC[-/C]AGCACCCTCAATGGC	9873
rs55633850	snp	A/G	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:73052599	GGAGAAACACTGTCG[A/G]AAATAAACAATGAAA	9873
rs55669705	snp	A/C	0.0379877	0.132479	intron-variant	FCHSD2	GRCh38.p7	11:72887346	ATACTACTGTGGACA[A/C]GAATGAAGACGGTGA	9873
rs55671951	snp	C/G	0.49917	0.0203505	intron-variant	FCHSD2	GRCh38.p7	11:72924063	CTCCCATTTTGTGGG[C/G]TGTCTTTTCACTTTC	9873
rs55691089	snp	A/G	0.0535932	0.154675	intron-variant	FCHSD2	GRCh38.p7	11:73136893	AAAAATTAGCCGGGC[A/G]TGGTGGCAGGTGTGG	9873
rs55702223	snp	C/T	0.00398564	0.0444627	intron-variant	FCHSD2	GRCh38.p7	11:72942703	TTGACAAACATGCTA[C/T]AGAATGTTATGGTAT	9873
rs55715883	in-del	-/TA			intron-variant	FCHSD2	GRCh38.p7	11:72980697	ATATATATATATATA[-/TA]ATGTATGTATGTATA	9873
rs55742663	snp	A/C	0.0441095	0.141807	intron-variant	FCHSD2	GRCh38.p7	11:72883143	AAAAAACCAAACATG[A/C]CCCTTAACTCATACC	9873
rs55744506	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:73110161	TCTTCTTTTTTTTTT[-/T]GATGTGTCTTTGGTC	9873
rs55755311	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:73131379	AAAAAAAAAAAAAAA[-/A]TTAGCCAGGCATGGT	9873
rs55787543	snp	C/T	0.0498117	0.149749	intron-variant	FCHSD2	GRCh38.p7	11:72918187	ATTTTCTTAACCTTC[C/T]TTTTGGATCATTCAT	9873
rs55810963	snp	C/T	0.0298908	0.118541	intron-variant	FCHSD2	GRCh38.p7	11:72916956	GGGTTCACAACTTCA[C/T]TGAACTTCATTCTTT	9873
rs55823053	snp	A/G	0.0755793	0.179102	intron-variant	FCHSD2	GRCh38.p7	11:72879719	TCAAACTGAGACTGA[A/G]ATAAAAAATAAGGCC	9873
rs55827213	in-del	-/A/AA			intron-variant	FCHSD2	GRCh38.p7	11:72870921	AAAAAAAAAAAAAAA[-/A/AA]GAATTCCCCCTTTGA	9873
rs55838097	snp	C/T	0.0372196	0.131242	intron-variant	FCHSD2	GRCh38.p7	11:73034933	TTAAAAAGGTCACTC[C/T]ACAGGCAGCTAAAGT	9873
rs55872828	snp	C/T	0.0150606	0.0854603	intron-variant	FCHSD2	GRCh38.p7	11:73110836	ACTTCGTACTGCTGT[C/T]GTTGTATCTCATGGG	9873
rs55888199	snp	C/T	0.0980852	0.198549	intron-variant	FCHSD2	GRCh38.p7	11:72998806	TAGGTGGCTATTATT[C/T]TTTAAAAGGATAACA	9873
rs55905425	snp	C/T	0.228547	0.249078	intron-variant	FCHSD2	GRCh38.p7	11:72870065	TCCATCATGTGCTTG[C/T]GTGCCTGTGTGCGTG	9873
rs55916551	in-del	-/A/AA	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72851124	AAAAAAAAAAAAAAA[-/A/AA]GGTTGCTAAGTGCTA	9873
rs55949049	snp	A/G	0.0418186	0.138422	intron-variant	FCHSD2	GRCh38.p7	11:72951401	GATAACACAGCAAAC[A/G]AGAGCGACAGATTAC	9873
rs55978850	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72923402	GTGACTGCAACATTT[A/T]ACCTTTCTACTAGCA	9873
rs56027064	snp	G/T	0.279991	0.248195	intron-variant	FCHSD2	GRCh38.p7	11:72852059	TTTTTGTTTTTGGTG[G/T]TTTTTTTTTGGTAGA	9873
rs56060052	snp	G/T	0.020002	0.0979842	intron-variant, downstream-variant-500B	FCHSD2, ATG16L2	GRCh38.p7	11:72836507	CGTATTTCTTTTTTT[G/T]CCCATGGGAAAAGCA	9873
rs56061370	in-del	-/TT	0.0295035	0.117819	intron-variant	FCHSD2	GRCh38.p7	11:72857454	TAAAATGCTTACTCC[-/TT]TTTTTTTTTTTTTTT	9873
rs56101807	in-del	-/TT	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72851878	ATCAGTCAGAGTGGC[-/TT]TTTTTTTTTTTTTTT	9873
rs56104404	in-del	-/GTT			intron-variant	FCHSD2	GRCh38.p7	11:73100378	GTTGTTGTTGTTGTT[-/GTT]TTGAGATGGAGTTTC	9873
rs56104779	in-del	-/A	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73133815	AAAAAAAAAAAAAAA[-/A]GTAACCATTATGCCA	9873
rs56133665	snp	C/T	0.0494327	0.149241	intron-variant	FCHSD2	GRCh38.p7	11:72964203	AGAAACAAAAACAAA[C/T]ATATCCTGACTATAA	9873
rs56166008	snp	A/T	0.281577	0.247998	intron-variant	FCHSD2	GRCh38.p7	11:73100223	AATGTACCAAGGACC[A/T]TTCCTCTTCGCGTCC	9873
rs56198813	in-del	-/A	0.334642	0.235236	intron-variant	FCHSD2	GRCh38.p7	11:73116952	TTTCCATTTTTCCCC[-/A]AAAAAAATCACTATT	9873
rs56200651	snp	A/C	0.0248432	0.108648	intron-variant	FCHSD2	GRCh38.p7	11:72990374	AATATCTGATAGGAA[A/C]CCTCCACCCCAAATC	9873
rs56271335	snp	C/T	0.225597	0.248806	intron-variant	FCHSD2	GRCh38.p7	11:72852254	TATGGAAAAAAGGGA[C/T]GCTTATACACTGCTG	9873
rs56281436	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:72846094	GATAGATAGATAGAT[-/A]AGTAGTTACGATTAC	9873
rs56283764	snp	A/G	0.0372196	0.131242	intron-variant	FCHSD2	GRCh38.p7	11:73048805	TCAAGAGAAAGGGTG[A/G]GGAATGAATATTTGC	9873
rs56294550	snp	C/T	0.00953873	0.0683987	intron-variant	FCHSD2	GRCh38.p7	11:72910535	TTACCCCCAACCCCA[C/T]GCTCTTTGAAACATG	9873
rs56316448	snp	C/G	0.0486741	0.148216	intron-variant	FCHSD2	GRCh38.p7	11:73099207	GCAATGGAGCAAGAC[C/G]CTGCTTCCAAAAATA	9873
rs56847486	in-del	-/CT			intron-variant	FCHSD2	GRCh38.p7	11:72968335	CTATAATTTATCATT[-/CT]GTTTCCTAGAAAATA	9873
rs56903801	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72968014	GAGAACGGCGTGAAC[C/T]TGGGAGGTGGAGCTT	9873
rs57018545	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72899702	GATTATGCCATTGCA[A/C]TTCAGTCTGGGTGAC	9873
rs57050252	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:73048072	AAAAGGCAGGAAGTT[-/A]AAAAAAAAATACAGG	9873
rs57079825	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72916183	GTTTACCTACATAAT[C/T]TGCACATCCTGCACA	9873
rs57081131	snp	A/G	0.0142736	0.0832652	intron-variant	FCHSD2	GRCh38.p7	11:72854956	CAGCCTGGCCAACAT[A/G]GTGAAACCCTATCTC	9873
rs57111296	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72896594	CGTTGATGAGATCCT[C/T]TTTGTGGAATAAGTA	9873
rs57248794	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72923658	TTTAAATTAGGTTGT[C/G]AGGTTGGGTGTGGTG	9873
rs57304246	in-del	-/A	0.444666	0.15686	intron-variant	FCHSD2	GRCh38.p7	11:72956825	ATGATTTCATAGTGG[-/A]AAAAAAAAAAAAACC	9873
rs57347063	in-del	-/TT	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72907619	TTTTTTTTTTTTTTT[-/TT]CTTGAGACGGAGTCT	9873
rs57436707	in-del	-/TT			intron-variant	FCHSD2	GRCh38.p7	11:72871772	TTTTTTTTTTTTTTT[-/TT]AGAGCCAGAGTGGTT	9873
rs57489704	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72971489	AGAGTTTTCTCTAGC[C/T]AGTAGCAAAAAAGTC	9873
rs57492987	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:72971375	AATCCCCTTTCCTTT[-/T]GAGTGTCAGTAGAAC	9873
rs57517075	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:72954223	TTTTTTTTTTTTTTT[-/T]GAGACAGGGTCTCAC	9873
rs57560627	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72861926	ACAAAAGCGAAACGC[C/T]GTCTCAAAAAAAAAA	9873
rs57566526	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:73048352	TAGTACTGGCTTGTT[-/T]ATTTACAGGTACTAG	9873
rs57571079	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72880068	AACCAAAACAAGACA[A/C]AAACAAACAAACAAA	9873
rs57731198	snp	G/T	0.0425829	0.139564	intron-variant	FCHSD2	GRCh38.p7	11:72980214	AGGTTTGAAGAGGGG[G/T]GAAAAGTTGAAATAA	9873
rs57741648	snp	C/T	0.0441095	0.141807	intron-variant	FCHSD2	GRCh38.p7	11:73116809	CTCAAAGTGCACGGA[C/T]TACAGGCATGAGCCA	9873
rs57864696	in-del	-/AT			intron-variant	FCHSD2	GRCh38.p7	11:73107052	TATATATATATATAT[-/AT]TTTTAAATGGAGTCT	9873
rs57890374	snp	A/T	0.00478085	0.0486577	intron-variant	FCHSD2	GRCh38.p7	11:73104697	CCTCAGCCTCCCAAG[A/T]AGCTGGGACCACAGG	9873
rs57926217	in-del	-/ATATTTATTTAT			intron-variant	FCHSD2	GRCh38.p7	11:72903207	TATTTATTTATTTAT[-/ATATTTATTTAT]TTATTTATTTATTTT	9873
rs57953662	snp	C/T	0.0829062	0.185956	intron-variant	FCHSD2	GRCh38.p7	11:73119358	TAGAATTCTGTATTA[C/T]GTAACTAGTGTATTA	9873
rs57970812	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72859891	GCACCCAGTAGAGTA[C/T]TAACATTAGTAAGGA	9873
rs58006230	snp	C/T	0.115438	0.210697	intron-variant	FCHSD2	GRCh38.p7	11:72897255	ATAGTTGTCCTTCCA[C/T]ATCTGTGGGTTCTGT	9873
rs58050555	snp	C/T	0.0825414	0.185628	intron-variant	FCHSD2	GRCh38.p7	11:73117731	TAACATCCATATAGC[C/T]GCCATTAGATTCTGC	9873
rs58059528	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73097719	TTTGTGTGTTTCTAA[A/G]ATTTATCTATTTCAC	9873
rs58159831	in-del	-/A	0.493477	0.0567349	intron-variant	FCHSD2	GRCh38.p7	11:72896790	AAAAAAAAAAAAAAA[-/A]GAAAGAAATATGCTT	9873
rs58432383	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:73063624	GAAAGCAAAAAAAAA[-/A]GCAGGAGTTGCAATC	9873
rs58451717	in-del	-/GT/GTGTGT	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72959885	TGTGTGTGTGTGTGT[-/GT/GTGTGT]ATGTGTGATATCAAT	9873
rs58496020	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72922643	TATAGATGACAAGTA[C/T]GTATCAAATAATTTT	9873
rs58773322	in-del	-/AAA			intron-variant	FCHSD2	GRCh38.p7	11:73004134	AAAAAAAAAAAAAAA[-/AAA]GGATATCAAGCATAT	9873
rs58891110	snp	A/C	0.00636936	0.0560724	intron-variant	FCHSD2	GRCh38.p7	11:73108623	CCGGACTGCGGACTG[A/C]AGTGGCGCAATCTCG	9873
rs58955891	in-del	-/TA	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72980696	ATATATATATATATA[-/TA]ATGTATGTATGTATA	9873
rs59059938	snp	C/T	0.0825414	0.185628	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72840778	CATCCTTGTTTGGCA[C/T]AGTCAGTAACAACAC	9873
rs59090297	snp	C/T	0.0271762	0.113356	intron-variant	FCHSD2	GRCh38.p7	11:72915690	GGGCGCGGTGGTGGG[C/T]GCCTATAATCCCAGC	9873
rs59105217	snp	G/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73087931	TCTCCCAAGCTGGAG[G/T]GCAGTGATGCAATCA	9873
rs59339008	in-del	-/GT/GTGT	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72959026	TGTGTGTGTGTGTGT[-/GT/GTGT]ACATCCATGCGTGCA	9873
rs59339955	snp	A/G	0.0916144	0.193427	intron-variant	FCHSD2	GRCh38.p7	11:72925513	CCTGGGCAACAGAGC[A/G]AGACCCTATCTTTAA	9873
rs59376387	in-del	-/C	0.0995161	0.199636	intron-variant	FCHSD2	GRCh38.p7	11:72959479	TGACCTCATGATCCG[-/C]CCGCCTCGGCCTCCC	9873
rs59486746	in-del	-/TT	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72872303	TTTTTTTTTTTTTTT[-/TT]AGAACCACACAATTC	9873
rs59566812	snp	A/G	0.0818113	0.184966	intron-variant	FCHSD2	GRCh38.p7	11:73012484	TACTTGATAAAAAAC[A/G]TGTATTACTTGGATA	9873
rs59574482	snp	C/T	0.0150606	0.0854603	intron-variant	FCHSD2	GRCh38.p7	11:72856833	GCCACATAAAAGAAT[C/T]ATGCTAGAAATTGCC	9873
rs59603567	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:73090243	TTTTTTTTTTTTTTT[-/T]GAGACGGAGTCTCGC	9873
rs59672416	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73061102	TTTCTGCATGTCCAA[C/T]TGAGGTACCTGGTTC	9873
rs59694859	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73097022	TTTTTTTTTTGATGA[A/G]ACAGGGTCTCACTCT	9873
rs59718560	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:72978874	TTTTTTTTTTTTTTT[-/T]GAGATGAAGTCTCAC	9873
rs59748827	in-del	-/A			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841364	AAAAAAAAAAAAAAA[-/A]GCAAATGCAGTTTTT	9873
rs59822793	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72847828	CTCCCTAGTAGCTGA[A/G]ATTACAGGCGCCCGC	9873
rs59887161	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:72906291	GTTTTTTTCTTGTAA[-/A]TTTGTTTAAGTCCTT	9873
rs59906199	in-del	-/GCTCAAT/TATAGAATACATGCTCAAT			intron-variant	FCHSD2	GRCh38.p7	11:72947758	ACATAATTTTCTCAT[-/GCTCAAT/TATAGAATACATGCTCAAT]AAAGAAAATTAAATA	9873
rs59925945	snp	C/G	0.0372196	0.131242	intron-variant	FCHSD2	GRCh38.p7	11:73031415	CGGGAGGTGGAGGCT[C/G]CATTGAGTTGTGACT	9873
rs60087749	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73081623	TCTCCGGCTCCAGGG[A/C]TCAAGCAACTCTCCT	9873
rs60091261	in-del	-/A			intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841341	GAGACTCTGTCTCCA[-/A]AAAAAAAAAAAAAAA	9873
rs60152221	in-del	-/C			intron-variant	FCHSD2	GRCh38.p7	11:72845462	AAAAAAAAAAAAAAA[-/C]AACAACAAACAAACA	9873
rs60219481	snp	C/T	0.0980852	0.198549	intron-variant	FCHSD2	GRCh38.p7	11:72997210	ATCAGAGCAGCTACA[C/T]GATGTTGAGAAGACA	9873
rs60223064	in-del	-/TTT	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73097016	TTTTTTTTTTTTTTT[-/TTT]GATGAGACAGGGTCT	9873
rs60281079	in-del	-/AGGA	0.00716266	0.059414	intron-variant	FCHSD2	GRCh38.p7	11:72966202	GTCGCCCAGGAAGGA[-/AGGA]GTGCAGTGGTGCGAT	9873
rs60288681	snp	C/G	0.0399052	0.1355	intron-variant	FCHSD2	GRCh38.p7	11:72862056	AGACTAAAAAAGAAC[C/G]ATTTGACAAGATCCA	9873
rs60355221	snp	A/G	0.498852	0.0239341	intron-variant	FCHSD2	GRCh38.p7	11:72854880	CGGTGGCTCATGCCT[A/G]TAATCCCAGCACTTT	9873
rs60386383	in-del	-/GATTATAGAATA			intron-variant	FCHSD2	GRCh38.p7	11:72947755	AAAACATAATTTTCT[-/GATTATAGAATA]CATAAAGAAAATTAA	9873
rs60397765	snp	C/T			upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73143683	TGAGATCCCAGACAG[C/T]TGTTCTCAGAAGTGC	9873
rs60470955	snp	A/G	0.0588605	0.161139	intron-variant	FCHSD2	GRCh38.p7	11:72866462	TTTAGTAGAGACAGC[A/G]TTTCACCATGTTGGC	9873
rs60568866	snp	A/C	0.0821764	0.185298	intron-variant	FCHSD2	GRCh38.p7	11:73037780	AATATAGGAGTCCTC[A/C]TTACCTTGTAACCCT	9873
rs60627587	snp	C/T	0.0399052	0.1355	intron-variant	FCHSD2	GRCh38.p7	11:72900688	ATTAAAAAAAAAAAG[C/T]ACTACTATAAAGGGC	9873
rs60656498	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72873514	GATTTGCAAATATTT[C/T]CCCCCATTCTGTGGG	9873
rs60718050	snp	C/G	0.0391387	0.134304	intron-variant	FCHSD2	GRCh38.p7	11:73006304	GTAGGCACCTTTACA[C/G]CTAACATGTACAAAA	9873
rs60755272	in-del	-/TTTTATATTCCCCACTCTATTTTATAT	0.349452	0.229367	intron-variant	FCHSD2	GRCh38.p7	11:72941468	TAGTATAAAATATAG[-/TTTTATATTCCCCACTCTATTTTATAT]ACTCCCAACTCTATT	9873
rs60812177	snp	C/T	0.0372196	0.131242	intron-variant	FCHSD2	GRCh38.p7	11:72999552	CTTGAATTCCTGACC[C/T]CAGGTGATCCACCCG	9873
rs60814034	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:72941405	ATTTATATAATTTTT[-/T]ATATTTATAAAAATA	9873
rs60877622	snp	C/T	0.0482946	0.147699	intron-variant	FCHSD2	GRCh38.p7	11:73026478	TATACCTTAAATATA[C/T]GCAATAAAATTTATT	9873
rs60886878	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:72879406	AACTTAGTAGGTATT[-/T]GAAAAGCAGAAAAAC	9873
rs60956838	snp	C/T			intron-variant, upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73140528	ATGGGGGCTGGGAGC[C/T]TAAGAGTGCCTGATA	9873
rs60989366	in-del	-/TT			intron-variant	FCHSD2	GRCh38.p7	11:72847709	TTTTTTTTTTTTTTT[-/TT]GAGACAGAGTCTCGC	9873
rs61049260	snp	C/T	0.0387552	0.1337	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841137	CCCACCACTGCACTC[C/T]AGCCTGGGTGACAGA	9873
rs61105502	in-del	-/AA/AAA	0.0115144	0.0749975	intron-variant	FCHSD2	GRCh38.p7	11:72900675	GATTAAAAAAAAAAA[-/AA/AAA]GCACTACTATAAAGG	9873
rs61212971	in-del	-/T			intron-variant	FCHSD2	GRCh38.p7	11:73005923	TTTTTTTTTTTTTTT[-/T]AAAGAGGCAGGGTCT	9873
rs61319356	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:72935715	ATCAGTTGATATAAA[-/A]GTAAAATCAGAAACA	9873
rs61424140	snp	C/T	0.0360663	0.129354	intron-variant	FCHSD2	GRCh38.p7	11:72997444	AGCCTCTACAGTTTT[C/T]ATCCACAATGTCCAA	9873
rs61440286	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72907565	CTAAATTTTGTTGAA[A/G]GCCTTTTCTGCATCT	9873
rs61450188	snp	A/C/T	0.0825414	0.185628	intron-variant	FCHSD2	GRCh38.p7	11:72931023	TTCACATTGCATGCC[A/C/T]GTATCAAAACATCTC	9873
rs61477672	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72918550	TTCCCTTCTATTCTA[A/G]TTTGCTGAGTGTTTA	9873
rs61511109	in-del	-/ACAC			intron-variant	FCHSD2	GRCh38.p7	11:73051913	CACACACACACACAC[-/ACAC]CCCACACACACTGAC	9873
rs61568147	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72944133	ATCCCTGATGAACAT[C/T]GATGCAAAAATCCTC	9873
rs61580317	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73051330	TAAAAAATAAAAAAA[A/T]AAAAAATTTAAATCT	9873
rs61586562	in-del	-/AAAAAA/AAAAAAAAAAAA	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73126370	AAAAAAAAAAAAAAA[-/AAAAAA/AAAAAAAAAAAA]TTCCACAATACAGAA	9873
rs61628747	snp	C/T	0.0345262	0.126772	intron-variant	FCHSD2	GRCh38.p7	11:72954073	TCACTTTGGCTATTA[C/T]GCAGAGAATAGACAT	9873
rs61753291	snp	C/T	0.0094476	0.0680775	synonymous-codon, nc-transcript-variant	FCHSD2	GRCh38.p7	11:72902630	CTGAAGATTGTAGTC[C/T]CGGACCACCTAAAGA	9873
rs61753292	snp	A/G	1.7967e-05	0.0029972	synonymous-codon, nc-transcript-variant	FCHSD2	GRCh38.p7	11:72889838	ACTTACCCGTTGTTG[A/G]TGAACAATGTTTTTA	9873
rs61894256	snp	A/G	0.5	0	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72837464	TGATTTCTTAACCAA[A/G]GAAAAAAAAAAAAAA	9873
rs61894258	snp	C/G	0.0107246	0.0724382	intron-variant	FCHSD2	GRCh38.p7	11:72856400	AAGTTTTAAAACTGA[C/G]TCTCCTCTTAACCAC	9873
rs61895228	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72864791	TCTTGGTATGGCTTT[G/T]GAATAAGAGAAGCAG	9873
rs61895229	snp	G/T	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:72870472	ATTCTTTCAAGATTG[G/T]CTCTACCAATCTTGA	9873
rs61895230	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72871776	TTTTTTTTTTTTTAG[A/T]GCCAGAGTGGTTGCT	9873
rs61895231	snp	A/C	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72893747	AGGGAGACTCTGTCT[A/C]CAAAAAAAAAAAAAA	9873
rs61895232	snp	A/G	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72897339	AAAAAAAAAAAAAAG[A/G]ATAGTTGTGTCTGTA	9873
rs61895233	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:72905900	GCCGCAATAAACATA[C/T]GTGTGCATGTGTCTT	9873
rs61895234	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:72910852	AAAAAAAAAAAAATT[A/T]CCTATAGAGTTGTTT	9873
rs61895235	snp	A/G	0.0252325	0.109451	intron-variant	FCHSD2	GRCh38.p7	11:72915388	TGACCCAGCAATCCC[A/G]TTACTGAGTATAACC	9873
rs61895236	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72917988	TCTGTAGATCACTTT[G/T]GGGAATATTACAATA	9873
rs61895238	snp	C/T	0.0158469	0.0875917	intron-variant	FCHSD2	GRCh38.p7	11:72924260	AGTTTTAAATTTTGA[C/T]GCAGTCTAATTTAGC	9873
rs61896228	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:72934042	TGAGCCTGGGAGGTT[G/T]AGGCTGCAGTGAGCC	9873
rs61896229	snp	G/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72941468	TTAGTATAAAATATA[G/T]ACTCCCAACTCTATT	9873
rs61896230	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72956840	AAAAAAAAAAAAAAC[A/C]AACCCTAGAAGACAC	9873
rs61896231	snp	A/G	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72971907	ACTGCAAAGGAACGA[A/G]AGATAAAAGTTTGGG	9873
rs61896232	snp	C/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72990044	TTTCCCAGAAGCTGT[C/T]AGGTGTTAAGAAAGG	9873
rs61896233	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:73003580	CAAGCTCCACCTCCC[A/G]GGTTCACGCCATTCT	9873
rs61896982	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73014150	TTTTTTTTTTTTTGG[G/T]AGACAGAGTCTCACT	9873
rs61896983	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:73036339	CAAAAAAAAAAAACC[A/C]AAGCTTCATAATCAC	9873
rs61896984	snp	C/T	0.0170251	0.090679	intron-variant	FCHSD2	GRCh38.p7	11:73039408	CTGTAGTCCTAGCTA[C/T]TCCAGAGGCAGAGGT	9873
rs61896985	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73045986	CTACAATAATTTCAG[A/T]AATTTTTTTTTTTTT	9873
rs61896986	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73046010	TTTTTTTTTTTTTAG[A/T]GACAGGGTCTCATTT	9873
rs61896987	snp	A/C	0.0225045	0.103662	intron-variant	FCHSD2	GRCh38.p7	11:73054801	CCCACCTCGGCCTCT[A/C]GAGTAGCTAGGACTA	9873
rs61896989	snp	A/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73095909	CTGACTGGCTGAGGA[A/T]TAAAAAAAAAAAAAG	9873
rs61896990	snp	C/T	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:73113976	CTAGGGCTCTACAAT[C/T]AGCAGGTGATAAAGC	9873
rs61896991	snp	A/G	0.0170251	0.090679	intron-variant	FCHSD2	GRCh38.p7	11:73118675	TCATTACTGATTTCT[A/G]TTTTCATTGCATGTG	9873
rs61896992	snp	C/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73121826	GCTGGGCTCCACTCT[C/T]AGAGTTCCTGATGCA	9873
rs61896993	snp	A/G	0.0142736	0.0832652	intron-variant	FCHSD2	GRCh38.p7	11:73138982	AAATACAGAATTAAA[A/G]TTGTAATTTTCAGTC	9873
rs66565959	in-del	-/ACTTGAGGT	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73039298	AGAGGTGGGCGGATC[-/ACTTGAGGT]CAGGAGTTGGAGACC	9873
rs67691008	in-del	-/ATTATAGAATACATGCTCA			intron-variant	FCHSD2	GRCh38.p7	11:72947757	AACATAATTTTCTCA[-/ATTATAGAATACATGCTCA]TAAAGAAAATTAAAT	9873
rs67901943	in-del	-/AAA	0.029116	0.117091	intron-variant	FCHSD2	GRCh38.p7	11:72938177	AAAAAAAAAAAAAAA[-/AAA]CTCCTTCATAATCTG	9873
rs68076887	in-del	-/TG			intron-variant	FCHSD2	GRCh38.p7	11:72959875	TGTGTGTGTGTGTGT[-/TG]GTGTGTGTGTATGTG	9873
rs71062793	in-del	-/AAAAAAAAAAAAAAAAA	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72916969	AAAAAAAAAAAAAAA[-/AAAAAAAAAAAAAAAAA]GAATGAAGTTCAATG	9873
rs71062794	in-del	-/C	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72956381	TTCCTTGTCAGACCT[-/C]CCACTCACCAGCCTT	9873
rs71458287	multinucleotide-polymorphism	AC/CA	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72913835	AAACCCCAAAAAAAA[AC/CA]AAAAAAAAAAACCCT	9873
rs71469444	in-del	-/G	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72902103	GGTCTTGAACTCCTG[-/G]ACCTCAGGTCATCCA	9873
rs71469445	in-del	-/C	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72902106	TCTTGAACTCCTGAC[-/C]TCAGGTCATCCACCT	9873
rs71469446	in-del	-/G	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72948711	CGCTCTGTCGCCCAG[-/G]CTGGAGTGCAGTGGC	9873
rs71469447	in-del	-/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73044315	AGTGTGGTGTCTTAT[-/T]ATCTGTAATCCCAAT	9873
rs71469448	multinucleotide-polymorphism	CC/GT	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73081365	GCTTGAACTTGGGAG[CC/GT]GGAGGGTGCAGTGAG	9873
rs71469449	in-del	-/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73126339	GCAAGATTCCATCTT[-/T]AAAAAAAAAAAAAAA	9873
rs71479508	snp	C/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72847370	ATTTGTTCATGCCTT[C/T]CATCATTCAAGTATT	9873
rs71479509	snp	A/C	0.277778	0.248452	intron-variant	FCHSD2	GRCh38.p7	11:72896762	AATTAGGGGGAAAAT[A/C]CTAAAAAAAAAAAAA	9873
rs71479510	snp	A/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72896800	AAAAAAGAAAGAAAT[A/T]TGCTTGCCTTGTGGA	9873
rs71479512	snp	A/G	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72961019	GAAAATGGTGACCTA[A/G]GAATGGGGAGGTAAC	9873
rs71479513	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72971300	AAATTTAACAAAATA[C/T]GTGAAGACTGCTGAA	9873
rs71479514	snp	A/C	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73042663	AGAATGGTCATGTTA[A/C]CAATGTTCATTCTTC	9873
rs71479515	snp	A/G	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73097188	TTGTATTTTTTCGTA[A/G]AGATGGGGTTTCACC	9873
rs71479516	snp	A/G	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73126383	AAATTCCACAATACA[A/G]AAAGAAAGGAATACA	9873
rs71479517	snp	A/G	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73126465	CAATCACTTTATGAA[A/G]AAAAGTTTGTAAATC	9873
rs71588180	in-del	-/A	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73063615	AAGCAAATGGAAAGC[-/A]AAAAAAAAAGAAAAA	9873
rs71686837	in-del	-/AA/AAA			intron-variant	FCHSD2	GRCh38.p7	11:72899757	TAAGACCCTATCTTA[-/AA/AAA]AAAAAAAAAAAAAAA	9873
rs71928324	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:73133793	GAGAAACTCCGTCTC[-/A]AAAAAAAAAAAAAAA	9873
rs72053185	in-del	-/A	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73083570	ATCTCAGAAAAAAAG[-/A]AAAAAAAAAAAACAA	9873
rs72054328	in-del	-/A			intron-variant	FCHSD2	GRCh38.p7	11:73039518	CTCCAAAAAAAAAAA[-/A]GAAAGAAAGAAAAGA	9873
rs72055490	in-del	-/ATA			intron-variant	FCHSD2	GRCh38.p7	11:73039926	TAATATTCATGAGGA[-/ATA]TATCACAAAAGCAGT	9873
rs72245982	in-del	-/AT			intron-variant	FCHSD2	GRCh38.p7	11:72980687	TGTGTATATATATAT[-/AT]ATATATATAATGTAT	9873
rs72270596	in-del	-/AAAC			intron-variant	FCHSD2	GRCh38.p7	11:72880069	AGACAAAAACAAACA[-/AAAC]AACAAACAAAAACCA	9873
rs72477723	snp	C/T	0.0379877	0.132479	intron-variant	FCHSD2	GRCh38.p7	11:73043975	AATTTTGGCAACAAA[C/T]TATTAGGTGAGTGAG	9873
rs72497002	snp	A/G	0.32	0.24	intron-variant	FCHSD2	GRCh38.p7	11:73065153	gcttgatcatgttgg[A/G]taagctttctgatgt	9873
rs72969821	snp	A/C	0.0154538	0.0865337	intron-variant, downstream-variant-500B	FCHSD2, ATG16L2	GRCh38.p7	11:72836438	CTCCCTCCTCAGCTG[A/C]CTCTATGCTATCTGC	9873
rs72969826	snp	C/T	0.0130921	0.0798413	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838284	CAGTCTGGGGACTAA[C/T]CTTGGGGAGGAGCCA	9873
rs72969835	snp	C/T	0.0138799	0.0821421	intron-variant	FCHSD2	GRCh38.p7	11:72854847	TAGATGAAAAGAATA[C/T]TAGAAATGGGCCAGG	9873
rs72969841	snp	C/G	0.0142736	0.0832652	intron-variant	FCHSD2	GRCh38.p7	11:72858706	AATAATCTGTACAAC[C/G]CCCCCATGACACAAG	9873
rs72969847	snp	C/T	0.0154538	0.0865337	intron-variant	FCHSD2	GRCh38.p7	11:72862394	GTGAGTTTAGCAAGA[C/T]TGCAGGATATAAGAT	9873
rs72969855	snp	C/G			intron-variant	FCHSD2	GRCh38.p7	11:72866127	TCCTGCTGTAGAAGC[C/G]CAAATCAAGTGGGCC	9873
rs72969865	snp	A/G	0.0154538	0.0865337	intron-variant	FCHSD2	GRCh38.p7	11:72873571	ATTTGAAACATGAAA[A/G]TTTTAAATTTTGATG	9873
rs72969872	snp	C/T	0.0479149	0.147179	intron-variant	FCHSD2	GRCh38.p7	11:72876986	CTTCATTTTTTTTTT[C/T]TTTAGACAGGGTCTG	9873
rs72969874	snp	C/T	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:72877589	AGTCTCTTAGAGATA[C/T]ATTTATTCTACATTC	9873
rs72969876	snp	C/G	0.284471	0.247612	intron-variant	FCHSD2	GRCh38.p7	11:72878733	GTGGAACTCCAGGAG[C/G]AGAGGCAAACAATAA	9873
rs72969880	snp	A/C	0.00874735	0.0655527	intron-variant	FCHSD2	GRCh38.p7	11:72880431	TGGAACAGAACAGAC[A/C]TCCCAGAAATAATGT	9873
rs72969893	snp	C/T	0.230603	0.249246	intron-variant	FCHSD2	GRCh38.p7	11:72883100	AACTGGCTATCTGTA[C/T]AGGAAAAAACAAAAC	9873
rs72969899	snp	C/T	0.228253	0.249052	intron-variant	FCHSD2	GRCh38.p7	11:72883460	AACTCAGTAATAAGA[C/T]CAATCTAAATTTGGG	9873
rs72977485	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72904682	GTTCTCAAATTTCCC[C/T]GATTGTTTCTTTTTT	9873
rs72977499	snp	A/G	0.0138799	0.0821421	intron-variant	FCHSD2	GRCh38.p7	11:72916709	TATCAGATATGTGAT[A/G]TGCAAATATTTTCTC	9873
rs72977501	snp	C/T	0.0471551	0.14613	intron-variant	FCHSD2	GRCh38.p7	11:72916807	CAGTCTAATTATCTA[C/T]GTTTTCTTTCGTTAC	9873
rs72979412	snp	C/T	0.281577	0.247998	intron-variant	FCHSD2	GRCh38.p7	11:72928351	GTCCCAACATAACTC[C/T]CTCTCATTAGCACCA	9873
rs72979428	snp	G/T	0.0150606	0.0854603	intron-variant	FCHSD2	GRCh38.p7	11:72935344	GGCACAGATTCTTCA[G/T]CAATAAAGTTTTGCT	9873
rs72979433	snp	C/G	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72936551	AGGCCAAGATGGGAG[C/G]CTTGCTTGAGGCCAG	9873
rs72981516	snp	G/T	0.152778	0.230321	intron-variant	FCHSD2	GRCh38.p7	11:72959855	TTTAAGTTTCTAGGG[G/T]GTGTGTGTGTGTGTG	9873
rs72981525	snp	A/G	0.0142736	0.0832652	intron-variant	FCHSD2	GRCh38.p7	11:72965138	AGATCCCCATTGCCT[A/G]TAGAACAATTCTTAA	9873
rs72981528	snp	A/T	0.0150606	0.0854603	intron-variant	FCHSD2	GRCh38.p7	11:72967612	CCAGGAACTAGGGAG[A/T]AGGGAGAACACAAAA	9873
rs72981532	snp	A/G	0.0142736	0.0832652	intron-variant	FCHSD2	GRCh38.p7	11:72973561	ATACTATCTAAGACA[A/G]CACTATCTATTGTCA	9873
rs72981539	snp	A/G	0.0146672	0.084371	intron-variant	FCHSD2	GRCh38.p7	11:72973985	TAGAGTGCAAATGAA[A/G]GAGCAATTAATTGTG	9873
rs72981540	snp	A/C	0.0154538	0.0865337	intron-variant	FCHSD2	GRCh38.p7	11:72976046	GAACAAATTATCTCA[A/C]CACAAACCAGCTGAG	9873
rs72981544	snp	A/G	0.0150606	0.0854603	intron-variant	FCHSD2	GRCh38.p7	11:72981002	TAACATTAATTCAGA[A/G]AAACAGATATTTTCA	9873
rs72982843	snp	A/G	0.0482946	0.147699	intron-variant	FCHSD2	GRCh38.p7	11:72999210	AGGTATACCCAATAT[A/G]TACTGAATATTTAAC	9873
rs72982844	snp	A/C	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72999878	TCAGACACACACACA[A/C]ACACACACAAACACA	9873
rs72982846	snp	A/C	0.381503	0.21262	intron-variant	FCHSD2	GRCh38.p7	11:72999888	ACACACACACACACA[A/C]ACACACACACACACA	9873
rs72982850	snp	C/T	0.278664	0.248351	intron-variant	FCHSD2	GRCh38.p7	11:73006240	TTCCTGCCCAGACAC[C/T]TTCCCTAAACCCTAA	9873
rs72982852	snp	A/G	0.279991	0.248195	intron-variant	FCHSD2	GRCh38.p7	11:73010783	AGTAGAGGCAGTGGT[A/G]AGTTGGCACTAGTAG	9873
rs72982854	snp	G/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:73012473	TACTGTTTACCTACT[G/T]GATAAAAAACATGTA	9873
rs72982856	snp	C/T	0.00874735	0.0655527	intron-variant	FCHSD2	GRCh38.p7	11:73015277	AGCCACGTCTAAATC[C/T]TTTGTTTATATTCAA	9873
rs72982858	snp	A/G	0.0146672	0.084371	intron-variant	FCHSD2	GRCh38.p7	11:73023467	TGTCATTACGGAAAT[A/G]CAAACTAAAATAATG	9873
rs72982860	snp	A/C	0.0146672	0.084371	intron-variant	FCHSD2	GRCh38.p7	11:73023468	GTCATTACGGAAATG[A/C]AAACTAAAATAATGT	9873
rs72982862	snp	C/G	0.0326105	0.123535	intron-variant	FCHSD2	GRCh38.p7	11:73024364	TAGCTAGAAACTGTA[C/G]GACTAAAGACAAAAA	9873
rs72982867	snp	C/T	0.281841	0.247964	intron-variant	FCHSD2	GRCh38.p7	11:73028582	GCATGAGTTAAGACT[C/T]TGGTGGACTGTTGAG	9873
rs72982879	snp	A/G	0.0138799	0.0821421	intron-variant	FCHSD2	GRCh38.p7	11:73036559	ACTAGCATACTGCAA[A/G]TCCCTGATAAATTAT	9873
rs72982892	snp	A/C	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:73047231	ATTTGAATTGTTAAA[A/C]CTACCATTTTTTTTT	9873
rs72982894	snp	C/T	0.0146672	0.084371	intron-variant	FCHSD2	GRCh38.p7	11:73060040	CTATCCTTACTAAAA[C/T]GTTCTTTTTAAAAGC	9873
rs72984904	snp	C/T	0.0146672	0.084371	intron-variant	FCHSD2	GRCh38.p7	11:73098684	GAAAGAATAGTCTCT[C/T]CAACAAATGGTGCCA	9873
rs72984908	snp	A/T	0.281313	0.248031	intron-variant	FCHSD2	GRCh38.p7	11:73106862	TTTGTGTAAGTACAT[A/T]CTATGATGTTGATAC	9873
rs72984911	snp	C/G	0.0146672	0.084371	intron-variant	FCHSD2	GRCh38.p7	11:73115551	CACTGGAGGGTGCAT[C/G]CATCAAGGTTCTTCA	9873
rs72984914	snp	A/G	0.0146672	0.084371	intron-variant	FCHSD2	GRCh38.p7	11:73115914	TCATGGCAACATGTA[A/G]ATTAACATTTGATTA	9873
rs72984920	snp	A/T	0.0325976	0.123435	intron-variant	FCHSD2	GRCh38.p7	11:73129629	GATTCTACAGTATAC[A/T]GGGTTGCATAATTGT	9873
rs72984921	snp	C/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:73134301	CATAGTGAAACCCTC[C/T]CTCTACAAAAAATAC	9873
rs72984922	snp	A/G	0.0138799	0.0821421	intron-variant	FCHSD2	GRCh38.p7	11:73137480	ATAGCTCCCCTACAG[A/G]GTGTATACAGTATCT	9873
rs72984924	snp	A/G	0.0482946	0.147699	intron-variant	FCHSD2	GRCh38.p7	11:73138974	AGGAAGACAAATACA[A/G]AATTAAAATTGTAAT	9873
rs72984927	snp	A/G	0.0134861	0.0810011	intron-variant, upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73141661	TTAGAGGACGGACGA[A/G]CCCCGGCGGCCCCTC	9873
rs73532927	snp	C/T	0.039522	0.134904	intron-variant	FCHSD2	GRCh38.p7	11:72913163	GATTTAATTACCTCC[C/T]ACTGGCCCCTCCTCC	9873
rs73532992	snp	C/T	0.0832709	0.186283	intron-variant	FCHSD2	GRCh38.p7	11:72927118	CCCTCTCTTCTTTTC[C/T]GGGTAGGCAAAAAAC	9873
rs73534926	snp	C/T	0.0456336	0.143994	intron-variant	FCHSD2	GRCh38.p7	11:72960942	ACACATACCTCTCAC[C/T]TACTATGTTTTCCTA	9873
rs73534943	snp	A/G	0.0821764	0.185298	intron-variant	FCHSD2	GRCh38.p7	11:73036263	AGTATTGGAGCCAAC[A/G]TAATAATTTTGAAAT	9873
rs73534945	snp	C/T	0.0119091	0.0762411	intron-variant	FCHSD2	GRCh38.p7	11:73036755	ACAAGGTACTAACAT[C/T]TCAACCCTCAAGAAG	9873
rs73536825	snp	A/G	0.105214	0.203807	intron-variant	FCHSD2	GRCh38.p7	11:73136417	ACACAAAAATTAGCC[A/G]CGCACCTGGAGTCTC	9873
rs74236680	snp	A/G			intron-variant	FCHSD2	GRCh38.p7	11:72862900	ATAGAACAGAACAAA[A/G]TGTCAAGAAACAGAC	9873
rs74236685	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73125769	GGAATAGCTAACAAA[C/T]GCAAAAAGAAAAAGA	9873
rs74236686	snp	A/G	0.0517044	0.152246	intron-variant	FCHSD2	GRCh38.p7	11:73130380	AAGGACTACAGGCAC[A/G]TGCTATGGTGCCAGA	9873
rs74388037	snp	A/G	0.0414363	0.137845	intron-variant	FCHSD2	GRCh38.p7	11:73002615	AAAAAATGAAAAAGA[A/G]CCATTATAAATTGTG	9873
rs74403126	snp	A/C	0.02016	0.0983543	intron-variant	FCHSD2	GRCh38.p7	11:73106493	TGCTTGTTAAAGAAC[A/C]CTGAAGTGCAAACTG	9873
rs74413406	snp	A/G	0.0322114	0.122752	intron-variant	FCHSD2	GRCh38.p7	11:72845270	TATGAAAAATACAAA[A/G]AATTGGTGGGTGTGG	9873
rs74439784	snp	A/T	0.24019	0.249807	intron-variant	FCHSD2	GRCh38.p7	11:72938351	AGTCGAGACTATTAG[A/T]CAAGGCTATTAGCAG	9873
rs74454619	snp	C/T	0.0275645	0.114116	intron-variant	FCHSD2	GRCh38.p7	11:72953732	ATGAAGAAAAGATGC[C/T]GCCTTATGTTGTGTA	9873
rs74454974	snp	A/G	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:73138346	ATAAGCTCCTGCACC[A/G]AGCTACAGACAACAG	9873
rs74458233	snp	A/G	0.0225045	0.103662	intron-variant	FCHSD2	GRCh38.p7	11:73023497	GTGGTACCACTACAC[A/G]TGTATTAGAATGCTA	9873
rs74502080	snp	G/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73092320	TTTTGTTTTTTTTTT[G/T]GTAGAGATGGGGTCT	9873
rs74534079	snp	A/C	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73122178	GCTAACTTAAAAGGC[A/C]AAAAAAAAAAATGTA	9873
rs74535400	snp	C/T	0.0279526	0.114869	intron-variant	FCHSD2	GRCh38.p7	11:73022417	CTGAGTTTAGCAAAG[C/T]TGCACAATACAACGT	9873
rs74540190	snp	A/G	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:72896642	GACTTTTAGTGATCA[A/G]TCCAATAAGGGAGTT	9873
rs74565092	snp	C/T	0.00914312	0.0669923	intron-variant	FCHSD2	GRCh38.p7	11:73095471	CAGACTCTCCCCTCT[C/T]CTCCAGTCAGAAATC	9873
rs74572269	snp	C/T	0.0441095	0.141807	intron-variant	FCHSD2	GRCh38.p7	11:72897136	CCACGCCCGGCCGTC[C/T]TGTGGAAAGATTTTA	9873
rs74593893	snp	C/T	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72897751	GTCAGCTGAATGACT[C/T]TAACATTGAGATCCT	9873
rs74597531	snp	A/G	0.0248432	0.108648	intron-variant	FCHSD2	GRCh38.p7	11:72963749	AGGGTTCTTACACCT[A/G]TGATAATCTAATTCT	9873
rs74597570	snp	C/T	0.000371035	0.0136154	intron-variant	FCHSD2	GRCh38.p7	11:72900242	CCTCCCGCCCTTGAC[C/T]CACACCCCATATACC	9873
rs74622394	snp	A/G	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73004137	AAAAAAAAAAAAAAA[A/G]GATATCAAGCATATA	9873
rs74641607	snp	A/G	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73132827	GAAACGGTAACAGAA[A/G]AAAAAAAAAAAAAAA	9873
rs74669541	snp	A/G	0.145642	0.227177	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72837090	GAACTGCTCTATTTA[A/G]TAAGCATTTGAAGAT	9873
rs74689480	snp	C/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73065304	TTTGACAAAATTCAA[C/T]AGCCCTTCATGCTAA	9873
rs74694323	snp	C/G	0.0138799	0.0821421	upstream-variant-2KB, nc-transcript-variant	FCHSD2	GRCh38.p7	11:73142663	GCCCTCCCTCCCCCA[C/G]GCTGGGAGCCAGCCG	9873
rs74697501	snp	A/G	0.00159617	0.0282053	intron-variant, utr-variant-3-prime, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72843613	ATGACAAAAACTGGG[A/G]ATCAAAATATTGAAA	9873
rs74703494	snp	A/G	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72895761	ATTGCTAATTCTAAA[A/G]CGCAACACTCATGTC	9873
rs74704910	snp	G/T	0.0479149	0.147179	intron-variant	FCHSD2	GRCh38.p7	11:73088692	ATTGGACTAAGAAAT[G/T]ATTATGACCAGCACT	9873
rs74740840	snp	C/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73025499	TCTCTCTCCTCCCAC[C/T]GTCCACCCTCAAGTA	9873
rs74790604	snp	A/C	0.00159617	0.0282053	intron-variant	FCHSD2	GRCh38.p7	11:72984951	TGAGTCAGTGACTTT[A/C]AAATGCTTCTCTAAG	9873
rs74810815	snp	C/T	0.0498117	0.149749	intron-variant	FCHSD2	GRCh38.p7	11:72918787	AAATGAACTTTGTTA[C/T]TAATTGGAAGGCATT	9873
rs74832985	snp	C/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73100876	GGATTTTTTTTTTTT[C/T]CCTTAATGCTGTTTA	9873
rs74833390	snp	G/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72871771	TTTTTTTTTTTTTTT[G/T]TTAGAGCCAGAGTGG	9873
rs74868804	snp	G/T	0.0539704	0.155153	intron-variant	FCHSD2	GRCh38.p7	11:72896368	TTTTGTGGACATGCA[G/T]GTTTCCCATATTATT	9873
rs74889640	snp	C/T	0.0267878	0.112589	intron-variant	FCHSD2	GRCh38.p7	11:73056632	TTAAATAAACATTCA[C/T]CATGCATTTAACACA	9873
rs74918179	snp	C/T	0.00716266	0.059414	intron-variant	FCHSD2	GRCh38.p7	11:72862259	TATTCAGCAATTTTA[C/T]AGTAAGAAGGAAAAA	9873
rs74933154	in-del	-/CAT			intron-variant	FCHSD2	GRCh38.p7	11:72914359	TTCCCATTGAACTAC[-/CAT]TGACATTCTTTGCAG	9873
rs74961842	snp	A/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72885127	TGGTCTAGTCCATCC[A/T]AAAATTTTATTATGA	9873
rs74977573	snp	C/T	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:73091765	CTAGCTGATGCTGGG[C/T]GTGGTGGCTCATGCC	9873
rs74977946	snp	C/T			intron-variant	FCHSD2	GRCh38.p7	11:73046211	TGCCCAGGCTACAAT[C/T]GAATTCCTGTGCTCA	9873
rs74999880	snp	C/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72966168	TCTTTGAACTGAGCC[C/T]TTTTTTTTTTTCAGT	9873
rs75013468	snp	C/T	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73017291	GCCAACGTATTACTT[C/T]TGGATAGGAATATAT	9873
rs75016670	snp	A/C	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72851105	TGACTCTGTCTCAAA[A/C]AAAAAAAAAAAAAAA	9873
rs75028414	snp	C/T	0.0498117	0.149749	intron-variant	FCHSD2	GRCh38.p7	11:72931014	TGTGCTTATTTCACA[C/T]TGCATGCCTGTATCA	9873
rs75028716	snp	A/G	0.00517822	0.0506191	intron-variant	FCHSD2	GRCh38.p7	11:73067610	ATCCCTGAAGCATTT[A/G]TAAGACCTGGTTCTA	9873
rs75029744	snp	A/G	0.0410537	0.137264	intron-variant	FCHSD2	GRCh38.p7	11:72979684	AAACATAGTATCTCA[A/G]AAAACTTACTTCCCA	9873
rs75037960	snp	G/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72851892	CTTTTTTTTTTTTTT[G/T]TTGAGATAGGGTCTT	9873
rs75058813	snp	A/G	0.32	0.24	intron-variant	FCHSD2	GRCh38.p7	11:73065160	GAAGCCAACTTGATC[A/G]TGTTGGGTAAGCTTT	9873
rs75065749	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:72956899	TCACCAGGGGTGAGA[C/T]AGTTTGACATCATGC	9873
rs75089889	snp	C/G	0.00716266	0.059414	intron-variant	FCHSD2	GRCh38.p7	11:72871320	ATCCCTGACATTCAA[C/G]CTTCTCAAAACCCTA	9873
rs75099005	snp	C/T	0.0513262	0.151752	intron-variant	FCHSD2	GRCh38.p7	11:73016861	CAGAATGTTTATCTA[C/T]AACAGGTGTCAGGGA	9873
rs75143804	snp	A/C	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72855476	GTGAGACTCCATCTC[A/C]AAAAAAAAAGAGTTC	9873
rs75147296	snp	A/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72887684	GACTAGTAGCCATAA[A/T]TTTTTTTCATTTATT	9873
rs75154584	snp	A/G	0.00835141	0.0640778	intron-variant	FCHSD2	GRCh38.p7	11:73098781	ATGGCTCAAAGACCT[A/G]AATGTAACAGCTAAA	9873
rs75171900	snp	C/T	0.0271762	0.113356	intron-variant	FCHSD2	GRCh38.p7	11:72998971	TATAAATCTGGCACA[C/T]TGGGGGTCACCATGT	9873
rs75187730	snp	A/C	0.000798403	0.0199641	intron-variant	FCHSD2	GRCh38.p7	11:72883217	CAAAGAAAAGCTTGA[A/C]CTATAACACTTCTAG	9873
rs75217445	snp	G/T	0.0444908	0.142359	intron-variant	FCHSD2	GRCh38.p7	11:72973366	GAGGAAAGCTCCATC[G/T]CAAAAAAAAAAGAAA	9873
rs75232987	snp	A/C	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73025481	TCCACTCTCAAGAGG[A/C]CCAAGTGTCTGTTGT	9873
rs75270017	snp	C/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73065293	GGCTGTTGAATTTTG[C/T]TGAAGGCCTTTTCTG	9873
rs75285179	snp	C/T	0.030278	0.119257	intron-variant	FCHSD2	GRCh38.p7	11:73132118	TGCATGAAGAGGCAA[C/T]GACAACTGCATCACA	9873
rs75287045	snp	A/G	0.0337553	0.125452	intron-variant	FCHSD2	GRCh38.p7	11:72846051	AAGGGATTACAAATA[A/G]ATAGATAGATAGATA	9873
rs75327146	snp	A/T	0.0023933	0.0345097	intron-variant	FCHSD2	GRCh38.p7	11:72905349	ATTTTGATACAGGAC[A/T]ACAATGTGTAATAAT	9873
rs75373975	snp	G/T	0.00318978	0.0398085	intron-variant	FCHSD2	GRCh38.p7	11:72957624	AACATCTCGTAAAAA[G/T]GTGTATTGGGTCTGT	9873
rs75379126	in-del	-/TA			intron-variant	FCHSD2	GRCh38.p7	11:73048781	CAGGGATGTATGTAT[-/TA]AGTTCACCTCAAGAG	9873
rs75391788	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:72970920	AAGCCAAGTGCAGAA[A/G]CTCCAGCTGACAGCC	9873
rs75401749	snp	G/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73004138	AAAAAAAAAAAAAAG[G/T]ATATCAAGCATATAC	9873
rs75407017	snp	C/T	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:73073606	GCTCACCTGTATGCT[C/T]TGTAAACCTCACAAA	9873
rs75409252	snp	C/T	0.0225045	0.103662	intron-variant	FCHSD2	GRCh38.p7	11:72857775	CTCTTATTGCAGAGG[C/T]AGGAAAGATGATCTT	9873
rs75428668	snp	C/T	0.0437281	0.141251	intron-variant	FCHSD2	GRCh38.p7	11:72911976	TCACATATAGAAATG[C/T]TACTTATTTTTGTAT	9873
rs75432004	snp	C/T	0.0123036	0.0774623	intron-variant	FCHSD2	GRCh38.p7	11:72981667	AAGTCTGAAGCACTA[C/T]GTAATACCTAATACG	9873
rs75460794	snp	A/C	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73045070	GCAAGACTCCATCTC[A/C]AAAAAAAAAAAAAAG	9873
rs75487611	snp	A/G	0.0414363	0.137845	intron-variant	FCHSD2	GRCh38.p7	11:73044696	AATTAGGCAAATGCT[A/G]GGTAAATACTATATA	9873
rs75516546	snp	C/G	0.0482946	0.147699	intron-variant	FCHSD2	GRCh38.p7	11:73001665	TATATAAACTGACGC[C/G]GCTGGAAAAATATAT	9873
rs75545303	snp	C/T	0.00716266	0.059414	intron-variant	FCHSD2	GRCh38.p7	11:73044317	GTGTGGTGTCTTATA[C/T]CTGTAATCCCAATGC	9873
rs75563167	snp	C/T	0.0399052	0.1355	intron-variant	FCHSD2	GRCh38.p7	11:72969059	AGATTTTCTTTGAAA[C/T]CAATTTAAAATAGTA	9873
rs75575551	snp	A/C	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73044271	CTCAATTAAAAAAAA[A/C]CTTATGAATATTTCC	9873
rs75578981	snp	A/G	0.0142736	0.0832652	intron-variant	FCHSD2	GRCh38.p7	11:73123683	GATCTTCTTAATTGC[A/G]TAACCATCCCCCTCC	9873
rs75589131	snp	A/G	0.00199481	0.0315187	intron-variant	FCHSD2	GRCh38.p7	11:73040306	GTTTCGCAGTCATGT[A/G]GAAAAACAAAAAGAG	9873
rs75590143	snp	A/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73081535	TAGACTTTTTTTCTA[A/T]TTTTTTTTTAGACAG	9873
rs75600642	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73104869	GGCCAACTTTACTAA[C/T]TGAAAGCAAGAGAGC	9873
rs75608106	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73092962	ATAGTCTATGCTAAC[A/T]ATGTGATTTCATCAG	9873
rs75614960	snp	G/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72888635	TTTCTTTTTTTTTTT[G/T]GGAGACAGGGTCTTT	9873
rs75629822	snp	C/T	0.0111196	0.0737302	intron-variant	FCHSD2	GRCh38.p7	11:72903966	GATAAGGGGGATATA[C/T]AGATGAATAAGACAA	9873
rs75634820	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73055179	AATTGAATCATGGGG[G/T]TGTTTTCCCCCATGC	9873
rs75645317	snp	C/T	0.0437281	0.141251	intron-variant	FCHSD2	GRCh38.p7	11:73127367	TGAAATTAACAAAAA[C/T]ACCAGCTAAGGTTCC	9873
rs75682240	snp	C/T	0.0482946	0.147699	intron-variant	FCHSD2	GRCh38.p7	11:73131839	TTTCATTTATACTTA[C/T]TAAAAGAGTTCTTTT	9873
rs75689385	snp	A/T			intron-variant	FCHSD2	GRCh38.p7	11:73066732	AACAGACATGAAAAA[A/T]TGCTCATCATCATTG	9873
rs75706799	snp	A/G	0.0379877	0.132479	intron-variant	FCHSD2	GRCh38.p7	11:73028849	CCTTTCGTTCTCTCC[A/G]TCTCTCCTGCCACCA	9873
rs75712846	snp	A/C	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72851101	AGCGTGACTCTGTCT[A/C]AAAAAAAAAAAAAAA	9873
rs75745992	snp	A/T	0.0111196	0.0737302	intron-variant	FCHSD2	GRCh38.p7	11:72870224	GTTAATAATTCCTTT[A/T]TCTCTGCTCCTAAAG	9873
rs75746175	snp	A/G	0.0566069	0.158427	upstream-variant-2KB	FCHSD2	GRCh38.p7	11:73143543	CGGGGGAGTTTATCG[A/G]CCTCCCTTGGGGTCC	9873
rs75772023	snp	A/C/G/T	0.0196033	0.0970431	intron-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841600	TGCAGCAAAGGGAAG[A/C/G/T]GAGGTTACCCGGTGC	9873
rs75792944	snp	A/G	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73126508	TACTTGTACATATTA[A/G]AAATAAATTTTAAAG	9873
rs75817245	snp	C/G	0.0107246	0.0724382	intron-variant	FCHSD2	GRCh38.p7	11:73071341	GCATGATTTCCAACC[C/G]CACCACCAACTTTGG	9873
rs75824287	snp	A/C	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73021247	ATAAAAAAAAAAAAA[A/C]ACAGGCACACATACG	9873
rs75829877	snp	C/T	0.0456336	0.143994	intron-variant	FCHSD2	GRCh38.p7	11:73112205	TTCCCCAGCTTTTGT[C/T]TGTCTGGAAAAGCCT	9873
rs75835200	snp	A/T	0.00358779	0.0422022	intron-variant	FCHSD2	GRCh38.p7	11:72927063	TAGTTTTTACTATCT[A/T]AACAATTCACAAGCA	9873
rs75838105	snp	A/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73064488	CTTCAAAAAAAAAAA[A/T]CAATGAATCCAGGAG	9873
rs75841466	snp	A/G	0.0429648	0.14013	intron-variant	FCHSD2	GRCh38.p7	11:72878564	TGTTTTACTAGGAAG[A/G]AAGTATTCAAGGACT	9873
rs75875624	snp	A/C	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72968091	GCAAGACTCTGTCTC[A/C]AAAAAAAAAAAAAAG	9873
rs75911233	snp	C/G	0.0298908	0.118541	utr-variant-3-prime, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72838731	GTGCCTAAAAAACAA[C/G]ACTGGCCAAACTCCA	9873
rs75960712	snp	A/G	0.0329836	0.124112	intron-variant	FCHSD2	GRCh38.p7	11:72856060	TGTTTACACATTTAA[A/G]GTTACAAAGAATGGA	9873
rs75964225	snp	A/G	0.0111196	0.0737302	intron-variant	FCHSD2	GRCh38.p7	11:72952795	TATTTACAATTCATG[A/G]AAAGGATATTGTTCA	9873
rs75983652	snp	G/T			intron-variant	FCHSD2	GRCh38.p7	11:73086246	AAACTCCGTCTCTAC[G/T]AAAAATACAAAAATT	9873
rs75998165	snp	A/G	0.0298908	0.118541	intron-variant	FCHSD2	GRCh38.p7	11:73027797	GCAGCCTTGGGACAC[A/G]GTGCCCTGCACCCCA	9873
rs76001876	snp	C/T	0.00265634	0.0363472	intron-variant	FCHSD2	GRCh38.p7	11:72984233	TAAAACATAGCAAAA[C/T]AAAATAATCAGTGCA	9873
rs76022679	in-del	-/TTTTTTTTTTTTTTTTTT			intron-variant	FCHSD2	GRCh38.p7	11:72916969	CATTGAACTTCATTC[-/TTTTTTTTTTTTTTTTTT]TTTTTTTTTTTTTTT	9873
rs76070544	snp	C/T	0.0372196	0.131242	intron-variant	FCHSD2	GRCh38.p7	11:73009946	TGGATGTCTAAATCT[C/T]GTTAGACTTGGGAAG	9873
rs76079323	snp	A/G			missense, intron-variant, nc-transcript-variant	FCHSD2, ATG16L2	GRCh38.p7	11:72841556	GCAGTGGAGGCAGGG[A/G]GGCGTGTGGCTTGGG	9873
rs76107225	snp	C/T	0.00517822	0.0506191	intron-variant	FCHSD2	GRCh38.p7	11:72851422	CTGATGTATCCATAT[C/T]ATAGATTAATAACAC	9873
rs76113203	snp	A/G	0.46875	0.121031	intron-variant	FCHSD2	GRCh38.p7	11:73065170	CACCACGATCAAGTC[A/G]GCTTCATCCCTGGGA	9873
rs76130853	snp	G/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:73129891	TTTTTTTTTTTTTTT[G/T]TGAGACAGAGTCTCG	9873
rs76139598	snp	C/T	0.0232847	0.105357	intron-variant	FCHSD2	GRCh38.p7	11:73121269	TTATCCCAGAAGGAG[C/T]TCTGGTAAATGCAAT	9873
rs76143439	snp	C/T	0.0103295	0.0711199	intron-variant	FCHSD2	GRCh38.p7	11:73015482	TCACCGTCACAATAA[C/T]GTGTTTCATCATAGG	9873
rs76144216	snp	C/T	0.0482946	0.147699	intron-variant	FCHSD2	GRCh38.p7	11:73103390	CATTGTTTCTGAAAA[C/T]TTAACCTGCTTCCAT	9873
rs76146800	snp	C/T	0.00755907	0.0610114	intron-variant	FCHSD2	GRCh38.p7	11:73047040	TATTTTTATCAATGA[C/T]AAAAAATACTATTAA	9873
rs76151517	snp	A/C	0.0479149	0.147179	intron-variant	FCHSD2	GRCh38.p7	11:73022211	GATAGAGATAAGGCA[A/C]AGATTTTCTCTGTTA	9873
rs76192428	snp	G/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:72876991	TTTTTTTTTTTTTTA[G/T]ACAGGGTCTGGACTT	9873
rs76212699	snp	A/G	0.0170251	0.090679	intron-variant	FCHSD2	GRCh38.p7	11:73081688	TGTGCCACTGCACTT[A/G]GCTAAAATAGCGTAT	9873
rs76217534	snp	A/T	0.0111196	0.0737302	intron-variant	FCHSD2	GRCh38.p7	11:73115158	TGCTCCCTCCATGAG[A/T]GGTCATTGGCTAAGT	9873
rs76221272	snp	G/T	0.00676609	0.0577691	intron-variant	FCHSD2	GRCh38.p7	11:73012717	AATTCTTCATCTCTC[G/T]CCCCCTGCTTCATTC	9873
rs76229346	snp	C/T	0.00119737	0.0244387	intron-variant	FCHSD2	GRCh38.p7	11:72851339	ATGTTTACTGCAACA[C/T]TGCCTGTAGTGACAA	9873
rs76256213	snp	G/T	0.5	0	intron-variant	FCHSD2	GRCh38.p7	11:73130502	CATGTCTATGAATCA[G/T]AAACTATCTTCACCT	9873
rs76266669	snp	C/T	0.000399281	0.0141238	intron-variant	FCHSD2	GRCh38.p7	11:73005419	TATCAGCAACACTGA[C/T]CTAGTTTATCCTTCT	9873
rs76276314	snp	A/G	0.0479149	0.147179	intron-variant	FCHSD2	GRCh38.p7	11:73072908	GTAAAAATAGCAAAA[A/G]ATTTTAGGTGCAACA	9873
rs76314706	snp	C/T	0	0	intron-variant	FCHSD2	GRCh38.p7	11:72934332	ATGAAGAGCCATGCC[C/T]TTTTTTTTTTTTTTT	9873
rs76365480	snp	C/G	0.0240643	0.107019	intron-variant	FCHSD2	GRCh38.p7	11:72942220	AAAAGAGCCTGGCAG[C/G]TCCCTCCTCTCTTGC	9873
rs76387017	snp	C/T	0.030278	0.119257	intron-variant	FCHSD2	GRCh38.p7	11:73012588	TAAGCTCCAAATAAA[C/T]AAAAACACTGGCAAT	9873
rs76404487	snp	C/T	0.0322114	0.122752	intron-variant	FCHSD2	GRCh38.p7	11:72936503	ATCTCGACCAGGTGC[C/T]ATGGCTCATGCCTGT	9873
rs76419506	snp	A/C			intron-variant	FCHSD2	GRCh38.p7	11:72881100	GCAAATATTTTCTCC[A/C]ATTTTACAGGTTGTC	9873
rs76426780	snp	A/T	0.0279526	0.114869	intron-variant	FCHSD2	GRCh38.p7	11:72861140	TAGAGATCCATATAA[A/T]TAATAAACCTCTAGC	9873
rs76437648	snp	C/T	0.0414363	0.137845	intron-variant	FCHSD2	GRCh38.p7	11:72959065	ACATCTCCTTACATA[C/T]CAGAATCTTGGGAGG	9873
rs76472077	snp	A/G	0.0126979	0.078662	intron-variant	FCHSD2	GRCh38.p7	11:73040022	TTCTCCCAGCAAAAT[A/G]GAGGACTTACGTTGA	9873
rs76518939	snp	A/G	0.0178098	0.0926698	intron-variant	FCHSD2	GRCh38.p7	11:73032014	TAAATTATGGTCATC[A/G]GTATGCTGCAATGTT	9873

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