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

FEM1B

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs1043378	snp	A/C			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68291300	AAAGGACTTTTAATC[A/C]CAGACAGTAGAATTA	10116
rs1227308	snp	A/G	0	0	intron-variant	FEM1B	GRCh38.p7	15:68285956	tggtattctgttcca[A/G]aaattgtgatcaaca	10116
rs1228663	snp	G/T	0	0	intron-variant	FEM1B	GRCh38.p7	15:68286044	tataggtctatactg[G/T]gtctctaatttttgt	10116
rs1228664	snp	G/T	0	0	intron-variant	FEM1B	GRCh38.p7	15:68286068	tttttgtatgtactg[G/T]gaggtaggaatcaag	10116
rs1236841	snp	A/G	0	0	intron-variant	FEM1B	GRCh38.p7	15:68285985	cactaaattcattaa[A/G]aatagtctatggctt	10116
rs3759822	snp	A/G	0.100588	0.200439	upstream-variant-2KB	FEM1B	GRCh38.p7	15:68275974	TAGAGATATGGAGAG[A/G]CAGAGAGAGATAGAA	10116
rs3837688	in-del	-/AGTCC			upstream-variant-2KB	FEM1B	GRCh38.p7	15:68276443	AGCCGAGCCCAGTCC[-/AGTCC]CTTGGAGCCACATAA	10116
rs3837689	in-del	-/GTTT			intron-variant	FEM1B	GRCh38.p7	15:68288883	AAAGTGAACATATTT[-/GTTT]ACTAGAGTCCCCTTT	10116
rs6494729	snp	C/T	6.58892e-05	0.00573936	synonymous-codon	FEM1B	GRCh38.p7	15:68290837	GCATCTGGCTGTCAA[C/T]TCCAATACTCCAGTT	10116
rs6494730	snp	G/T	0.368119	0.220336	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68292218	AAGGAACCAGGATAT[G/T]TTTGAATTTTTTCAC	10116
rs7172290	snp	A/T			intron-variant	FEM1B	GRCh38.p7	15:68280209	GTGGCAATTAAAAGA[A/T]CCTGAAATGACTAGA	10116
rs7172340	snp	A/G	0.0498117	0.149749	intron-variant	FEM1B	GRCh38.p7	15:68288463	CTAGCACAGTAGACT[A/G]TCTCCAGCAAAAATC	10116
rs7174574	snp	C/T	0.299411	0.245069	intron-variant	FEM1B	GRCh38.p7	15:68289052	tgttatctgttcata[C/T]tgtgtgtggagcagt	10116
rs7174848	snp	A/G	0.02016	0.0983543	intron-variant	FEM1B	GRCh38.p7	15:68283776	AATCAGTTTGGAAAC[A/G]TTCTTTAAATTGAAA	10116
rs7175297	snp	A/G	0.368938	0.219895	intron-variant	FEM1B	GRCh38.p7	15:68284190	gtgcccagccCTCAT[A/G]TAAACTTTTTAGTTA	10116
rs8027628	snp	G/T	0.271702	0.249056	intron-variant	FEM1B	GRCh38.p7	15:68285991	attcattaagaatag[G/T]ctatggctttttttt	10116
rs10152450	snp	G/T	0.368529	0.220116	intron-variant	FEM1B	GRCh38.p7	15:68279141	AGTGGGCTGCTGGGC[G/T]TTAATGTCAAAATAA	10116
rs11630865	snp	A/G	0.299664	0.245017	intron-variant, utr-variant-5-prime	FEM1B	GRCh38.p7	15:68278826	CACTTCATCTTCCAG[A/G]GCTAATAATCCATCC	10116
rs11632503	snp	C/T	0	0	intron-variant	FEM1B	GRCh38.p7	15:68280332	aacacctactgcgtg[C/T]taggttctgtGGTAG	10116
rs11636081	snp	A/G	0.0314385	0.121371	intron-variant	FEM1B	GRCh38.p7	15:68287727	tcaaggtgccagtag[A/G]ttcagttgtctggtg	10116
rs12594282	snp	A/T	0.00199481	0.0315187	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68295329	CAAGCTTGCCAAATG[A/T]TGAAATGAACAAGAT	10116
rs12909277	snp	A/G	0.445724	0.155538	intron-variant	FEM1B	GRCh38.p7	15:68288574	GATCAGACTCTAGCA[A/G]TAGTCTAATTTTGTA	10116
rs16951723	snp	C/T	0.368324	0.220226	upstream-variant-2KB	FEM1B	GRCh38.p7	15:68277673	AGCAGAACCTTTCTC[C/T]ACCGGGCCCGCGTGT	10116
rs28498450	snp	C/T			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68294590	TAAGCAGAAGCGTTT[C/T]TTTTTTTTTTTTGGA	10116
rs28728467	snp	C/G			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68294902	GCTGTGTGTCCATTC[C/G]TACTCTGAAAATGCA	10116
rs34021140	snp	C/T	0.0367231	0.130434	synonymous-codon	FEM1B	GRCh38.p7	15:68291044	TAGCCTAGTTGAAGC[C/T]GGAGCTCACACTGAC	10116
rs34503084	in-del	-/T			intron-variant	FEM1B	GRCh38.p7	15:68286682	TAGAAGTCTTGTGCA[-/T]TTTTTCATTAGATTT	10116
rs34601322	in-del	-/C	0.0279526	0.114869	intron-variant	FEM1B	GRCh38.p7	15:68285785	CAGTCCTCTTCTTAG[-/C]CCCCCCCGCAGTGCT	10116
rs34693034	snp	C/T	0.299664	0.245017	intron-variant	FEM1B	GRCh38.p7	15:68282497	TGAACCAGGCATTTC[C/T]ATTTCAGATTGAACC	10116
rs34728807	in-del	-/C			intron-variant	FEM1B	GRCh38.p7	15:68284875	TGTAAGGGGGAGATT[-/C]CCCTGCACAAGCTCA	10116
rs34917142	snp	A/C/G	0.00683764	0.0580695	synonymous-codon	FEM1B	GRCh38.p7	15:68290021	TGGCCATGGGATGAC[A/C/G]CCATTGAAAGTAGCT	10116
rs34999248	in-del	-/T			intron-variant	FEM1B	GRCh38.p7	15:68285928	TTTAACGGTTAATGC[-/T]TTTTTTTTTTTTTGG	10116
rs35187853	in-del	-/T	0.32955	0.237006	intron-variant	FEM1B	GRCh38.p7	15:68283886	TAATCTCACGTAAAC[-/T]TTTTTTTTTTTTTTT	10116
rs35242796	snp	A/C			intron-variant	FEM1B	GRCh38.p7	15:68286162	TTCTACCTGAATTTC[A/C]CTGGAGCCTTTGTCA	10116
rs35278866	in-del	-/C			utr-variant-5-prime, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278302	GCGGCGGCGACGGCG[-/C]CCCTGTTGAATGGGC	10116
rs35445025	in-del	-/G			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68293430	TTATTTATAAAATGA[-/G]GAATAATGATTATAT	10116
rs35486786	in-del	-/A			intron-variant	FEM1B	GRCh38.p7	15:68288932	TCACTACCTCTCCCC[-/A]AAAGTAACCAGTATC	10116
rs35525989	snp	C/G/T	0.00675318	0.0577161	synonymous-codon, utr-variant-5-prime	FEM1B	GRCh38.p7	15:68289730	AACTAATTCAACCCC[C/G/T]CTGCGGGCAGCATGC	10116
rs35576212	snp	C/T	0.163892	0.234703	intron-variant	FEM1B	GRCh38.p7	15:68286789	ACATAATCATGACAA[C/T]AAAAACATAACAAAA	10116
rs35599421	snp	A/G	0	0	utr-variant-5-prime, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68277949	AGGGCGGAAAGCGCA[A/G]GAGGAGGCAGTGTTA	10116
rs35606342	snp	C/T	0.00927954	0.0674808	synonymous-codon, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278456	ATACAAGGCGGCCAG[C/T]GAGGGCAAGGTGCTG	10116
rs35616110	in-del	-/C			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68292108	TTGTCCCCTTTTCCC[-/C]TTTTTCTCCTGTATC	10116
rs35616559	in-del	-/T			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68294500	AATTAAAATTTCAAG[-/T]TGAGCAACACCCTGT	10116
rs35629462	in-del	-/C			intron-variant	FEM1B	GRCh38.p7	15:68283808	AATGTTTGAACAATG[-/C]ATGTGTACTATGTTT	10116
rs35888855	in-del	-/A			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68292366	AAATTTTTCAACCAC[-/A]AAAATGTCACTTATT	10116
rs35987978	in-del	-/A			frameshift-variant, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278449	CTATGTATACAAGGC[-/A]GGCCAGCGAGGGCAA	10116
rs55700060	snp	A/G	0.368733	0.220005	intron-variant	FEM1B	GRCh38.p7	15:68282112	AGGGGGAGGTGTCAT[A/G]TGACCATGAAACATT	10116
rs55722829	snp	A/G	0.0209421	0.100162	intron-variant	FEM1B	GRCh38.p7	15:68282024	AAGTCACATGAGTGG[A/G]AATGAAAGAAGATCC	10116
rs55941639	snp	A/G	0.368324	0.220226	utr-variant-5-prime, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68277828	GGAGCGTTCCGCATC[A/G]CCCCGGGGGCCCCTA	10116
rs57074540	snp	A/G	0.00953873	0.0683987	intron-variant	FEM1B	GRCh38.p7	15:68289528	AGTGAGGTCTTGGTC[A/G]GTGGGAGTGAATACA	10116
rs57128886	snp	A/G	0.113685	0.209567	intron-variant	FEM1B	GRCh38.p7	15:68287937	CTCCCAGGTTCAAGC[A/G]ATTCTCTTGCCTCAG	10116
rs58268546	in-del	-/CACA	0.5	0	intron-variant	FEM1B	GRCh38.p7	15:68286495	ACACACACACACACA[-/CACA]TATACCACACAACCT	10116
rs58402939	snp	C/T	0.0479149	0.147179	intron-variant	FEM1B	GRCh38.p7	15:68279447	TTTTTGGGTATTTGA[C/T]CAGAATTGTCAGGTT	10116
rs58984440	in-del	-/AG	0.112631	0.208878	intron-variant	FEM1B	GRCh38.p7	15:68281806	ATTTTTAGTAGAGAC[-/AG]GGTTTCACCGTGTTA	10116
rs59231560	snp	A/G	0.093417	0.194889	upstream-variant-2KB	FEM1B	GRCh38.p7	15:68277461	CCCTTCCCTAACCCC[A/G]GCTCAGGGGCAGAAG	10116
rs59705963	snp	G/T	0.0376037	0.131863	intron-variant	FEM1B	GRCh38.p7	15:68284542	GTATATCATATCTAG[G/T]AAAGTACATGAATCT	10116
rs60111545	in-del	-/T			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68292649	TAGCTTTTTTTTTTT[-/T]CTTTAATGAAAAGCA	10116
rs60432847	in-del	-/A			intron-variant	FEM1B	GRCh38.p7	15:68283532	AAAAAAAAAAAAAAA[-/A]GGTAGTATGCAGGAG	10116
rs60647108	snp	A/C	0.0482946	0.147699	intron-variant	FEM1B	GRCh38.p7	15:68280580	GCTGTGTTTTAAAGA[A/C]TAGTAGTAGGACATG	10116
rs60705177	snp	A/G	0.0991586	0.199366	downstream-variant-500B	FEM1B	GRCh38.p7	15:68296231	TTTCTATATGTATAG[A/G]TTTTTAAAACAACTT	10116
rs62003787	snp	C/T	0.5	0	intron-variant	FEM1B	GRCh38.p7	15:68279964	AACTCCTTGCATTCC[C/T]GCACCTAGAGAAGGA	10116
rs66989829	snp	G/T	0.272241	0.249009	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68292880	GAGGGGACAGAAGGG[G/T]GGACTATCCCCCAAG	10116
rs67342571	snp	A/G	0.368938	0.219895	intron-variant	FEM1B	GRCh38.p7	15:68281419	TCTTAGCTTCATCCC[A/G]TGTAATTATGGGTTT	10116
rs71455588	in-del	-/C	0.5	0	intron-variant	FEM1B	GRCh38.p7	15:68285792	CTTCTTAGCCCCCCC[-/C]GCAGTGCTGGGATTA	10116
rs71455589	in-del	-/T	0.5	0	intron-variant	FEM1B	GRCh38.p7	15:68287852	TTTTTTTTTTTTTTT[-/T]GAGATGAAGTTTTGC	10116
rs71726193	in-del	-/CA			intron-variant	FEM1B	GRCh38.p7	15:68286475	TCGACCTCTTGGACT[-/CA]CACACACACACACAC	10116
rs72038688	in-del	-/TAACA			intron-variant	FEM1B	GRCh38.p7	15:68286797	ATGACAATAAAAACA[-/TAACA]AAAAAATAACAAAAG	10116
rs72741150	snp	C/T	0.00517822	0.0506191	intron-variant	FEM1B	GRCh38.p7	15:68279472	CAGGTTTGACATTAT[C/T]CTCTTTTCTATGCTG	10116
rs72741151	snp	A/G	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68281309	GCTTCATAATTTTTG[A/G]CCAAATTGTTCACTA	10116
rs72741152	snp	A/G	0.0103295	0.0711199	intron-variant	FEM1B	GRCh38.p7	15:68282514	TTTCAGATTGAACCA[A/G]GTAATAGATGAGCTC	10116
rs73427899	snp	A/T	0.0726307	0.176182	upstream-variant-2KB	FEM1B	GRCh38.p7	15:68276204	GCTACCAGTAGAATC[A/T]TACCTTCAGCCCTTA	10116
rs74019863	snp	C/T	0.0185938	0.0946107	upstream-variant-2KB	FEM1B	GRCh38.p7	15:68276635	TTGCCTTCCAGAGTT[C/T]ATTCTCCATACAGCA	10116
rs74019864	snp	C/T	0.0217236	0.101931	upstream-variant-2KB	FEM1B	GRCh38.p7	15:68276927	ACCGTCTGTTCTTGT[C/T]ACTTGTCATAGAGGT	10116
rs74019865	snp	A/G	0.112983	0.209108	intron-variant	FEM1B	GRCh38.p7	15:68279271	TATATTGGCTACTAA[A/G]ATGGCATTGGACCTG	10116
rs74019866	snp	C/T	0.112983	0.209108	intron-variant	FEM1B	GRCh38.p7	15:68279934	TTTCCTTACTGGCTT[C/T]CGTGTCTTCTCTGTA	10116
rs74019867	snp	A/G	0.112983	0.209108	intron-variant	FEM1B	GRCh38.p7	15:68280013	TGAACCTCCAGTACC[A/G]TTCCACCTGTATAGG	10116
rs74019868	snp	C/T	0.112983	0.209108	intron-variant	FEM1B	GRCh38.p7	15:68280031	CCACCTGTATAGGCA[C/T]ATGAAGTCATTGAGA	10116
rs74019869	snp	C/T	0.113685	0.209567	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68292113	CCCCTTTTCCCTTTT[C/T]CTCCTGTATCTTTTA	10116
rs74019870	snp	A/G	0.113334	0.209338	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68292187	CTAATAAGGTATTTT[A/G]CTTATGACAGATGAA	10116
rs74019871	snp	G/T	0.113334	0.209338	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68293541	TGAAATGCTGACAGG[G/T]TGGAGAACGAATTTG	10116
rs74019872	snp	C/T	0.0539704	0.155153	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68294252	CTAGTAGCCCACAGC[C/T]CAATCACGTTAAGGT	10116
rs74370426	snp	G/T	0.112983	0.209108	intron-variant	FEM1B	GRCh38.p7	15:68283533	AAAAAAAAAAAAAAA[G/T]GTAGTATGCAGGAGG	10116
rs74483643	snp	C/T	0.0349115	0.127424	intron-variant	FEM1B	GRCh38.p7	15:68288888	GAACATATTTGTTTA[C/T]TAGAGTCCCCTTTGT	10116
rs74521321	snp	C/T	0.00398564	0.0444627	utr-variant-5-prime, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278200	CCGCCTTCCTCCCTG[C/T]GCGGGCTGGGTCGCG	10116
rs75191224	snp	C/T	0.107341	0.205301	intron-variant	FEM1B	GRCh38.p7	15:68285071	ATACAGCTTCTGTCA[C/T]CACAGATTAGTTTTG	10116
rs75471612	snp	C/T	0.0209421	0.100162	intron-variant	FEM1B	GRCh38.p7	15:68285020	TAAGTTGCCCAGTTT[C/T]GGGTATGCCTTTATC	10116
rs75545657	snp	C/T	0	0	intron-variant	FEM1B	GRCh38.p7	15:68285704	GTCTTTTTTTTTTTT[C/T]CTTAAATTGAGTAGA	10116
rs75571734	snp	A/G	0.0283406	0.115616	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68293457	ATATGTACATATTCA[A/G]ACATCAAAATTTAAT	10116
rs75959834	snp	C/T	0.0165278	0.0893908	intron-variant, utr-variant-5-prime	FEM1B	GRCh38.p7	15:68278987	AGGTGGCTGCCTTTC[C/T]AGGTTTTACTTTTAG	10116
rs76552257	snp	G/T	0.00636936	0.0560724	intron-variant	FEM1B	GRCh38.p7	15:68287688	ATTTATTTCTCATAT[G/T]TCTGGAAGCTGGAAT	10116
rs77020709	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68292367	AAATTTTTCAACCAC[A/T]AAATGTCACTTATTC	10116
rs77026141	snp	A/G	0.00953873	0.0683987	intron-variant	FEM1B	GRCh38.p7	15:68285897	TTAATGAAATCCAAT[A/G]AATACTTTCTTTTTC	10116
rs77594247	snp	A/C			missense	FEM1B	GRCh38.p7	15:68290481	GCCCTGCACCTCAGA[A/C]AAAAAGGTAACAGGA	10116
rs77747303	snp	C/T	0.00835141	0.0640778	upstream-variant-2KB	FEM1B	GRCh38.p7	15:68277528	TCCTTAGCCCATCAG[C/T]TTAGCGCCCTCACTC	10116
rs77832887	snp	C/T	0.5	0	intron-variant	FEM1B	GRCh38.p7	15:68285705	TCTTTTTTTTTTTTT[C/T]TTAAATTGAGTAGAG	10116
rs78230835	snp	A/C	0.0119091	0.0762411	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68295023	TGCCCAAATCTTTAG[A/C]TGGGCTGGGTTATAC	10116
rs78238174	snp	A/G	0.0562307	0.157967	upstream-variant-2KB	FEM1B	GRCh38.p7	15:68277604	AGGAGGAGGTTCCAG[A/G]AGTCAAGGACATTGA	10116
rs78511923	snp	G/T	0.0287284	0.116357	intron-variant	FEM1B	GRCh38.p7	15:68288621	TAGCACATATCAGAT[G/T]TTTAGTAAGTAAGTG	10116
rs78587299	snp	C/T	0.5	0	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68292649	GTAGCTTTTTTTTTT[C/T]CTTTAATGAAAAGCA	10116
rs79213461	in-del	-/TGTTT			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68291517	GGAACAGATATAAAA[-/TGTTT]TGTTTATGTAACAAG	10116
rs79452366	snp	A/G	0.00795532	0.062565	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68295806	AATTTGAAACTAACA[A/G]TCTTGCTGTGTAAAA	10116
rs79638346	snp	A/C	0.113334	0.209338	intron-variant	FEM1B	GRCh38.p7	15:68281520	CTATTCTACCTAAAA[A/C]CTTCTATAATACCTT	10116
rs79699752	snp	C/T	0.0629771	0.165899	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68294949	GTCATCTCTTGAAAG[C/T]AGAAAACTCCTATGT	10116
rs79731779	snp	A/G	0.0295035	0.117819	intron-variant	FEM1B	GRCh38.p7	15:68288307	TTTTCCACTTCATGG[A/G]GGATATAATTTGACC	10116
rs79903143	snp	C/T	0.0349115	0.127424	intron-variant	FEM1B	GRCh38.p7	15:68288295	AGCATTATTCTCTTT[C/T]CCACTTCATGGGGGA	10116
rs80042059	snp	A/G/T	0.0299138	0.118727	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68294437	AGTAAAATATGATTT[A/G/T]GGGGCAGCAGCTTTC	10116
rs80143225	snp	G/T	0.02016	0.0983543	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68292923	TTTTTACAGTTGCTA[G/T]CATTATACTTTGTCT	10116
rs80174561	snp	A/C	0.00835141	0.0640778	upstream-variant-2KB	FEM1B	GRCh38.p7	15:68277215	AGATTCCTGCTCTGT[A/C]TGAACGCGGGACTCG	10116
rs80224911	snp	A/G	0.0271762	0.113356	intron-variant	FEM1B	GRCh38.p7	15:68279293	TTGGACCTGATGTGG[A/G]AGATGATGCCATTCT	10116
rs111294065	snp	A/C	0.0217236	0.101931	intron-variant	FEM1B	GRCh38.p7	15:68283358	TGTTTCCTGGCATAT[A/C]ATAATTATATGTTTT	10116
rs111343207	snp	A/G			splice-acceptor-variant	FEM1B	GRCh38.p7	15:68289605	ATTCTTTTCATGTGT[A/G]GGTATGTCATTGATG	10116
rs111367704	in-del	-/C	0.113334	0.209338	intron-variant	FEM1B	GRCh38.p7	15:68288408	GAATATTCCTTTGAT[-/C]AACCTTTCTTCTTAA	10116
rs111535011	snp	A/G	0.0356815	0.128715	intron-variant	FEM1B	GRCh38.p7	15:68283019	CAATAGAAATAGGTA[A/G]TTGGAACTTTTTTGA	10116
rs111558288	snp	C/T	0.5	0	missense	FEM1B	GRCh38.p7	15:68290059	GCTGTAAAGCTGATG[C/T]CGTAGAACTGTTACT	10116
rs111662065	snp	C/T	0.5	0	synonymous-codon	FEM1B	GRCh38.p7	15:68291131	AATACTGCTTAAAAC[C/T]CAAATGAAGATGAGT	10116
rs111677476	in-del	-/CAT	0.112631	0.208878	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68294311	AACCCCAAAGCAGAC[-/CAT]CATCTGTAAGCTTTG	10116
rs112104100	in-del	-/AT	0.107341	0.205301	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68293773	TAGAATTGTTTGAAA[-/AT]ATGTTTAGCCAGACC	10116
rs112190675	snp	C/T	0.5	0	intron-variant	FEM1B	GRCh38.p7	15:68289557	CATCCCTTAAACATA[C/T]GTTAGGCTGTGGCCT	10116
rs112281402	snp	A/C	0.5	0	upstream-variant-2KB	FEM1B	GRCh38.p7	15:68277127	AATATTCATTGGATA[A/C]ACGATCGTTTCAAAT	10116
rs112285240	snp	C/T	0.5	0	synonymous-codon	FEM1B	GRCh38.p7	15:68290621	GGAAATAGAACAAAG[C/T]ATGAACAGAGTGAAA	10116
rs112320487	in-del	-/A	0.112983	0.209108	intron-variant	FEM1B	GRCh38.p7	15:68279676	GCTAAAACTCGACTG[-/A]AAAAAACATTTCTTC	10116
rs112492149	snp	A/G/T	0.00199481	0.0315187	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68292480	TGTGATTATCTTTTA[A/G/T]GCATTACAGAAATTC	10116
rs112773498	in-del	-/T	0.5	0	intron-variant	FEM1B	GRCh38.p7	15:68285927	TTTAACGGTTAATGC[-/T]TTTTTTTTTTTTTTG	10116
rs112808051	snp	C/G/T	0.5	0	upstream-variant-2KB	FEM1B	GRCh38.p7	15:68277055	TCATTTGTTGACTTA[C/G/T]TTGTTCCATTACTGA	10116
rs112963437	snp	C/T	0.5	0	missense	FEM1B	GRCh38.p7	15:68291121	GGGTATCTGAAATAC[C/T]GCTTAAAACTCAAAT	10116
rs112967560	in-del	-/TTTG	0.113334	0.209338	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68293602	ATGGTAATTAGATTT[-/TTTG]TTTGTTTGTTTAGTA	10116
rs113167440	snp	C/T	0.5	0	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68293912	TGGTCATTTGATGTT[C/T]ACTATTGGTATACTT	10116
rs113170705	snp	A/G	0.5	0	intron-variant	FEM1B	GRCh38.p7	15:68289375	AGGTTTGTTTTTTAG[A/G]GTTATATACTCTAGT	10116
rs113503896	snp	A/G	0.00279162	0.0372561	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68295264	CAGCTTTTATTCAGG[A/G]TGAGTCATGTGATGA	10116
rs113521146	snp	A/C	0.0551013	0.156571	intron-variant	FEM1B	GRCh38.p7	15:68287014	TGCCTCAGCCTCCTG[A/C]GTAGCTGGGATTACA	10116
rs113550016	in-del	-/T	0.126909	0.217598	intron-variant	FEM1B	GRCh38.p7	15:68281624	TGAGTTCTTGTTCAC[-/T]TTTTTTTTTTTGAGA	10116
rs113911201	snp	C/T	0.5	0	intron-variant	FEM1B	GRCh38.p7	15:68284026	GAGTAGCTGGGATTA[C/T]AGACATGCGCCACCA	10116
rs113968932	snp	A/C	0.5	0	intron-variant	FEM1B	GRCh38.p7	15:68284620	AGTCACTCTCTAGAT[A/C]AATGTGTAGAACACT	10116
rs114115920	snp	C/T	0.02016	0.0983543	intron-variant, utr-variant-5-prime	FEM1B	GRCh38.p7	15:68278868	GCCCGTCCTCATCAG[C/T]CCCTACCCCTCATTC	10116
rs114194564	snp	C/T	0.0168055	0.0901129	upstream-variant-2KB	FEM1B	GRCh38.p7	15:68277282	AGCGCAGCTCCCCTT[C/T]GCTCCCATCTTTCTC	10116
rs114499684	snp	C/T	0.0205511	0.0992634	intron-variant	FEM1B	GRCh38.p7	15:68287186	ATAAGCCACCGCACC[C/T]GGCCTGATTCATTCT	10116
rs114824392	snp	A/G	0.0174175	0.0916809	upstream-variant-2KB	FEM1B	GRCh38.p7	15:68277360	CCTTCTCAGAGCCTG[A/G]TGTTGTGGCTCTCAA	10116
rs115117264	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	FEM1B	GRCh38.p7	15:68275947	AGAGGGAGGGTGGTA[A/G]GGAGACGGAGTTAGA	10116
rs115243221	snp	C/T	0.02016	0.0983543	intron-variant	FEM1B	GRCh38.p7	15:68283635	GCAGTGATTGTGCCA[C/T]TGTACTTAGCCGGTA	10116
rs115301451	snp	C/G	0.0209421	0.100162			GRCh38.p7	15:68275766	AGAAGGGGCCTGTGT[C/G]TGGACTTTTTTACAT	10116
rs115389215	snp	A/G	0.00716266	0.059414	intron-variant	FEM1B	GRCh38.p7	15:68280987	TACAAATTAATTAAT[A/G]AAAGAGATATTGAAG	10116
rs115820186	snp	C/T	0.0189856	0.0955633	intron-variant	FEM1B	GRCh38.p7	15:68288133	CCATGCCAGGCCTAA[C/T]GCCTCTTGTGTGTGG	10116
rs116437536	snp	A/G	0.00358779	0.0422022	intron-variant	FEM1B	GRCh38.p7	15:68286757	TTTTGACAATAAATA[A/G]ATGTTTATTGAACTT	10116
rs116529867	snp	G/T	0.299158	0.245119	utr-variant-5-prime, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68277820	CTCTTGCGGGAGCGT[G/T]CCGCATCGCCCCGGG	10116
rs116622280	snp	A/G	0.0209421	0.100162	intron-variant	FEM1B	GRCh38.p7	15:68285895	TTTTAATGAAATCCA[A/G]TAAATACTTTCTTTT	10116
rs117016386	snp	A/T	0.0178098	0.0926698	intron-variant	FEM1B	GRCh38.p7	15:68284207	AAACTTTTTAGTTAT[A/T]TATCTGCATAATAGT	10116
rs117027713	snp	G/T	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68281288	TTTTTAGTCATTCAC[G/T]TGCTAGCTTCATAAT	10116
rs117112835	snp	C/G	0.00517822	0.0506191	intron-variant, utr-variant-5-prime	FEM1B	GRCh38.p7	15:68278877	CATCAGCCCCTACCC[C/G]TCATTCCCTCTGTGG	10116
rs117261438	snp	A/G	0.0165278	0.0893908	intron-variant	FEM1B	GRCh38.p7	15:68283727	AACTATGTAATTGTT[A/G]CTATGTATTAACTTT	10116
rs117429382	snp	A/C	0.00914312	0.0669923	intron-variant	FEM1B	GRCh38.p7	15:68289242	CTGGGAAGGAGGAAC[A/C]TGCTGTTCTCCTAGT	10116
rs117462645	snp	C/T	0.0165278	0.0893908	intron-variant	FEM1B	GRCh38.p7	15:68280522	AAGTGCTGTTTTATC[C/T]GGGGGGAATCTAGAA	10116
rs117515767	snp	C/G	0.0271762	0.113356	intron-variant	FEM1B	GRCh38.p7	15:68284794	CCTGGTGGGAGGCAA[C/G]TGAATCATGGAAGCA	10116
rs117810047	snp	C/G	0.00398564	0.0444627	intron-variant	FEM1B	GRCh38.p7	15:68282661	ATAATAGAGAACTTG[C/G]ATTGTAATTTTGGAC	10116
rs137978210	snp	C/T	0.000992145	0.0222506	synonymous-codon, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278579	CCTCATCATCGCAGC[C/T]CGCAATGGACACGCA	10116
rs138024522	snp	A/G	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68281098	AAAAAAGAGTGTGAT[A/G]ATTTCACTTTGCATT	10116
rs138070159	snp	A/T	0.00279162	0.0372561	intron-variant	FEM1B	GRCh38.p7	15:68289465	TGCTTTCCTTAAATT[A/T]CCTGTTTTTATTTTC	10116
rs138222642	snp	C/T	0.00835141	0.0640778	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68293901	TGCAGCCACTTTGGT[C/T]ATTTGATGTTTACTA	10116
rs138242609	snp	C/T	0.000798403	0.0199641	intron-variant	FEM1B	GRCh38.p7	15:68279915	AACCTGATTCATGTT[C/T]GCTTTTCCTTACTGG	10116
rs138661188	snp	C/T			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68295550	CATCCTGCAATCCTC[C/T]GTGCAGAGGAACTAC	10116
rs138848316	snp	C/G	0.00119737	0.0244387	intron-variant	FEM1B	GRCh38.p7	15:68284665	GTTTCCCTTGTGCCC[C/G]TTCTCAGTTTCCTCC	10116
rs138874263	in-del	-/TATA	0.0271762	0.113356	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68294807	GTTTTTCTCACTGAC[-/TATA]TAACATTAAAAAGGG	10116
rs138890248	snp	C/T	0.0205511	0.0992634	intron-variant	FEM1B	GRCh38.p7	15:68287816	GGCAAGCCAGCGGAA[C/T]GTTGCTAACGTCTCT	10116
rs138980106	snp	A/C/T	9.90171e-05	0.00703561	missense	FEM1B	GRCh38.p7	15:68289986	GAGCTGATAAAATGG[A/C/T]GTGCTGCTATAGTAG	10116
rs139049383	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	FEM1B	GRCh38.p7	15:68276540	CTTTCATATTGAGTT[C/T]TTTGAGACTGTCCCA	10116
rs139084362	snp	C/T	0.00636936	0.0560724	downstream-variant-500B	FEM1B	GRCh38.p7	15:68296321	CTTTTAGATTTTCAG[C/T]TTTTGATATTTCAAA	10116
rs139085346	in-del	-/ATTTGGTATAAATTACCAAAGTA	0.039522	0.134904	intron-variant	FEM1B	GRCh38.p7	15:68284348	AGTGCTTGGCACTGT[-/ATTTGGTATAAATTACCAAAGTA]ATTTGGTATAAATTA	10116
rs139115473	snp	C/G	0.0566069	0.158427	intron-variant	FEM1B	GRCh38.p7	15:68281836	AGCCAGGATGGTCTC[C/G]ATCTCCTGACCTCGT	10116
rs139322594	snp	A/G	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68279348	TTGTGGGGAAGCTTG[A/G]TCATTTACTGTTAGT	10116
rs139474050	snp	C/T	0.0205511	0.0992634	utr-variant-5-prime, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68277861	CGAGGATCTCCGGGG[C/T]CGTTGGCAGCGCCTG	10116
rs139755237	snp	A/G	0.000131913	0.00812029	missense	FEM1B	GRCh38.p7	15:68290082	CTGTTACTCTCTCAT[A/G]CTGATTGCGACCGAA	10116
rs140096080	snp	C/G	1.65507e-05	0.00287664	missense, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278562	GGGCAGCGCTCCACG[C/G]CCCTCATCATCGCAG	10116
rs140169831	snp	A/G	0.00105477	0.0229406	synonymous-codon	FEM1B	GRCh38.p7	15:68290486	GCACCTCAGACAAAA[A/G]GGTAACAGGAACACC	10116
rs140387651	snp	A/G	0.000798403	0.0199641	intron-variant	FEM1B	GRCh38.p7	15:68286413	AGAGGTTCTCGCACT[A/G]TTGCTCAGGCAAGAG	10116
rs140441270	snp	A/G	1.66843e-05	0.00288823	missense	FEM1B	GRCh38.p7	15:68289906	CTGATCCCAATGCCA[A/G]AGCACATTGTGGAGC	10116
rs140469089	snp	A/T	0.00199481	0.0315187	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68291476	ATTTGCATATTGGTT[A/T]CCTATTTGTCTTTCT	10116
rs140609546	snp	A/G	0.00676609	0.0577691	intron-variant	FEM1B	GRCh38.p7	15:68287817	GCAAGCCAGCGGAAC[A/G]TTGCTAACGTCTCTT	10116
rs140986731	in-del	-/T	0.0193772	0.0965046	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68294904	GTGTGTCCATTCCTA[-/T]CTCTGAAAATGCATA	10116
rs141134172	snp	C/T	0.00119737	0.0244387	downstream-variant-500B	FEM1B	GRCh38.p7	15:68295911	AGTGTGCCTTAGTTG[C/T]GATGTTCTTTTGTTG	10116
rs141136497	in-del	-/T	0.0174175	0.0916809	intron-variant	FEM1B	GRCh38.p7	15:68283126	ACCAAGTAGTTTCCA[-/T]TATAAAAACCAAGTG	10116
rs141165548	snp	A/T	0.00636936	0.0560724	intron-variant	FEM1B	GRCh38.p7	15:68284264	ATAATAGGGCATAAT[A/T]ATAGTACCTACCTCA	10116
rs141232900	snp	A/G	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68288523	GAAATTTAGAAATTA[A/G]GGTTGGGGAAAAATT	10116
rs141234260	snp	C/T	0.00636936	0.0560724	intron-variant	FEM1B	GRCh38.p7	15:68287360	TTCCCTAAATATCCA[C/T]GTGGCTGCTACCCAG	10116
rs141272774	snp	C/T	0.00676609	0.0577691	upstream-variant-2KB	FEM1B	GRCh38.p7	15:68276974	AACTAAATGAGTGCC[C/T]CCATCATTCTATTTC	10116
rs141424379	snp	C/T	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68279353	GGGAAGCTTGATCAT[C/T]TACTGTTAGTTGAGG	10116
rs142077319	snp	A/G	0.0174175	0.0916809	intron-variant	FEM1B	GRCh38.p7	15:68281507	AGTTTTAAAAAGTCT[A/G]TTCTACCTAAAACCT	10116
rs142144377	snp	C/T	0.000164736	0.0090742	synonymous-codon	FEM1B	GRCh38.p7	15:68290873	TTTCCACACCAATGA[C/T]GTCTGCAGCTTTCCA	10116
rs142496932	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	FEM1B	GRCh38.p7	15:68278810	CTGCCCCACTAATGC[C/T]CACTTCATCTTCCAG	10116
rs142530350	snp	C/T	0.00795532	0.062565	intron-variant	FEM1B	GRCh38.p7	15:68281256	AGCTGTGTGCTGAAG[C/T]AGATTAGTGTTTCTA	10116
rs142597284	snp	C/T	0.0138799	0.0821421	intron-variant	FEM1B	GRCh38.p7	15:68284889	TTCCCTGCACAAGCT[C/T]ACTTTGCCTGCTGCC	10116
rs142755987	snp	A/G	0.00123696	0.0248385	missense	FEM1B	GRCh38.p7	15:68289987	AGCTGATAAAATGGC[A/G]TGCTGCTATAGTAGT	10116
rs142803256	snp	C/T	1.64904e-05	0.00287139	synonymous-codon	FEM1B	GRCh38.p7	15:68290060	CTGTAAAGCTGATGT[C/T]GTAGAACTGTTACTC	10116
rs142905378	snp	A/G	8.2464e-05	0.00642069	missense	FEM1B	GRCh38.p7	15:68290095	ATGCTGATTGCGACC[A/G]AAGAAGTCGGATTGA	10116
rs142985848	in-del	-/TGTT	0.02016	0.0983543	intron-variant	FEM1B	GRCh38.p7	15:68284511	GTTTTTAATTATATC[-/TGTT]TTTTTAGTGGAGGTA	10116
rs143176785	in-del	-/C	0.0023933	0.0345097	intron-variant	FEM1B	GRCh38.p7	15:68279761	CAATAAAAGCTTTTT[-/C]TTCTATTTTAGATGA	10116
rs143444897	snp	A/T	0.000153988	0.00877328	missense	FEM1B	GRCh38.p7	15:68290659	CAGATGCTGATGTCC[A/T]CAATGCTATGGACAA	10116
rs143456679	snp	C/T	0.0115649	0.0751578	intron-variant	FEM1B	GRCh38.p7	15:68289560	CCCTTAAACATATGT[C/T]AGGCTGTGGCCTCTG	10116
rs143544235	snp	C/T	0.00636936	0.0560724	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68293870	GCCCTCTGTGAACTC[C/T]AGGCTGTCTCCATTT	10116
rs143637660	snp	C/G	0.0118072	0.0759221	synonymous-codon	FEM1B	GRCh38.p7	15:68290834	GCTGCATCTGGCTGT[C/G]AATTCCAATACTCCA	10116
rs143677381	snp	C/T	0.00318978	0.0398085	intron-variant	FEM1B	GRCh38.p7	15:68283946	GCTAAAGTGCAATGG[C/T]GTGATCTTGGCTCAC	10116
rs143728777	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68293953	TTGTAAATCTTCATT[A/G]ATGGTATTACAGATT	10116
rs144092522	snp	C/T	0.00795532	0.062565	upstream-variant-2KB	FEM1B	GRCh38.p7	15:68276031	GAGGTGCATGCTTGC[C/T]GTATGGAGCCAGAAA	10116
rs144153679	snp	C/T	0.00676609	0.0577691	upstream-variant-2KB	FEM1B	GRCh38.p7	15:68277776	GTCTGCGAAAGCTCG[C/T]CTTCCTCCCCGCCCA	10116
rs144375722	in-del	-/AACAT	0.298651	0.24522	intron-variant	FEM1B	GRCh38.p7	15:68286793	AATCATGACAATAAA[-/AACAT]AACAAAAAAATAACA	10116
rs144468118	snp	A/G	1.64822e-05	0.00287068	missense	FEM1B	GRCh38.p7	15:68290377	TTTTAGGTGCTGACA[A/G]TATTGATGTTTCTCA	10116
rs144468787	snp	C/G	0.00164766	0.0286551	synonymous-codon	FEM1B	GRCh38.p7	15:68290075	CGTAGAACTGTTACT[C/G]TCTCATGCTGATTGC	10116
rs144579746	snp	C/T	0.00557542	0.0525036	intron-variant	FEM1B	GRCh38.p7	15:68285391	CAAGGAGTGGAATTG[C/T]TGGGTCATCAGGTAG	10116
rs144745637	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	FEM1B	GRCh38.p7	15:68276701	CTTGTCACTTCCCTC[C/T]TTAAAACCCTTCAAA	10116
rs144854183	snp	C/T	0.00597247	0.0543191	intron-variant	FEM1B	GRCh38.p7	15:68286584	GACATCTTAACATTA[C/T]AGAGTCTTCTGGATC	10116
rs145066007	snp	A/G	0.00597247	0.0543191	intron-variant	FEM1B	GRCh38.p7	15:68284531	TTTTAGTGGAGGTAT[A/G]TCATATCTAGTAAAG	10116
rs145141929	snp	C/T	0.00636936	0.0560724	intron-variant	FEM1B	GRCh38.p7	15:68282232	GGAGAATAGGACCTC[C/T]GAGAATTTTGAGGCT	10116
rs145232632	snp	C/T	0.00517822	0.0506191	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68291950	GATGGACTCTGCCTT[C/T]AGGCTTGAATTCTTC	10116
rs145390601	snp	C/T	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68287180	ACAGGCATAAGCCAC[C/T]GCACCCGGCCTGATT	10116
rs145530056	snp	C/T	0.00716266	0.059414	utr-variant-5-prime, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278196	CTGACCGCCTTCCTC[C/T]CTGCGCGGGCTGGGT	10116
rs145992598	snp	C/G	0.0123036	0.0774623	intron-variant	FEM1B	GRCh38.p7	15:68284907	TTTGCCTGCTGCCAT[C/G]CATGTAAGATGTGAC	10116
rs146034870	snp	C/G	0.0146672	0.084371	intron-variant	FEM1B	GRCh38.p7	15:68281431	CCCATGTAATTATGG[C/G]TTTGCTGTGTGTTTT	10116
rs146070259	snp	A/G	0.00953873	0.0683987	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68294280	GGTTCTTTGCTGTGG[A/G]AATTTTAAATAAACC	10116
rs146078795	snp	A/C	0.00993419	0.0697739	intron-variant	FEM1B	GRCh38.p7	15:68280373	TGCAGAGATGAATAA[A/C]ATACTCTTTTGTCTT	10116
rs146114767	snp	A/C	0.00065925	0.0181436	synonymous-codon, utr-variant-5-prime	FEM1B	GRCh38.p7	15:68289734	AATTCAACCCCCCTG[A/C]GGGCAGCATGCTTTG	10116
rs146122343	in-del	-/G	0.02016	0.0983543	intron-variant	FEM1B	GRCh38.p7	15:68286070	TTGTATGTACTGTGA[-/G]GGTAGGAATCAAGGT	10116
rs146241560	snp	C/G	0.00755907	0.0610114	upstream-variant-2KB	FEM1B	GRCh38.p7	15:68277217	ATTCCTGCTCTGTCT[C/G]AACGCGGGACTCGCT	10116
rs146447031	snp	C/G	0.00676609	0.0577691	upstream-variant-2KB	FEM1B	GRCh38.p7	15:68276291	GATCTGCAATAAGTG[C/G]GTAAAGCTGAGCTGT	10116
rs146502335	snp	A/C	0.0626037	0.165477	utr-variant-5-prime, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68277822	CTTGCGGGAGCGTTC[A/C]GCATCGCCCCGGGGG	10116
rs146784770	snp	G/T	0.000798403	0.0199641	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68291328	TTATGTGTTCATAAA[G/T]TCTGCTTTTCTTTCC	10116
rs146906047	snp	A/G	0.00358779	0.0422022	intron-variant, utr-variant-5-prime	FEM1B	GRCh38.p7	15:68278960	ATAGTCTGTGAACAA[A/G]CCATTTGGAGGAGGT	10116
rs146933937	in-del	-/TGT	0.272511	0.248984	intron-variant	FEM1B	GRCh38.p7	15:68282258	AGGCTTTTTGTTGAG[-/TGT]TGTTCTTTTAAAGTC	10116
rs147100682	snp	A/G/T	0.00275255	0.0369959	utr-variant-5-prime, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278411	GGTGTTGGAGTTGGC[A/G/T]GCGGCCATGGAGGGC	10116
rs147134863	snp	A/C	1.64963e-05	0.00287192	missense, utr-variant-5-prime	FEM1B	GRCh38.p7	15:68289695	GTCAGCCATGGAGCC[A/C]ACGTGAACCATACCA	10116
rs147171339	snp	C/T	0.0166325	0.0896639	intron-variant	FEM1B	GRCh38.p7	15:68286360	TCTTTTTTGAATTGG[C/T]CTGTCAGTTCTTTCT	10116
rs147577178	snp	A/G	0.0174175	0.0916809	intron-variant	FEM1B	GRCh38.p7	15:68282426	TTAAGGACTTTGGTT[A/G]AAATAAAGTGTGGAT	10116
rs147717192	snp	A/G	1.6549e-05	0.0028765	missense, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278616	GTACGCTTGCTCTTA[A/G]AACATTACCGGGTGC	10116
rs148088686	snp	C/T	0.0240643	0.107019	intron-variant	FEM1B	GRCh38.p7	15:68284164	TGTTGGGATTACAGA[C/T]GTGAGCCACTGTGCC	10116
rs148249211	snp	A/G	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68288286	AGCACCAGGAGCATT[A/G]TTCTCTTTTCCACTT	10116
rs148403753	snp	A/G	0.00199481	0.0315187	intron-variant	FEM1B	GRCh38.p7	15:68285829	TGAGCCACTGCACCT[A/G]GCCACTTAATCGCTT	10116
rs148495013	snp	C/G	0.000153988	0.00877328	missense	FEM1B	GRCh38.p7	15:68290045	AGTAGCTGCCGAAAG[C/G]TGTAAAGCTGATGTC	10116
rs148525584	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	FEM1B	GRCh38.p7	15:68276794	GCATCCTCTGACTTC[A/C]TCTATCATTCTTACT	10116
rs148564851	snp	A/C	0.00329293	0.0404428	synonymous-codon	FEM1B	GRCh38.p7	15:68290094	CATGCTGATTGCGAC[A/C]GAAGAAGTCGGATTG	10116
rs148686181	snp	A/G	0.00119737	0.0244387	intron-variant	FEM1B	GRCh38.p7	15:68281468	GTGCGTGAGAAAGAC[A/G]TACATTAAAATAAAT	10116
rs148913869	snp	C/T	3.30038e-05	0.00406212	synonymous-codon	FEM1B	GRCh38.p7	15:68290550	TCACAAATGATACAT[C/T]TGAATGAAACTGTGA	10116
rs149005836	snp	A/G	0.00636936	0.0560724	intron-variant	FEM1B	GRCh38.p7	15:68283806	ACAAATGTTTGAACA[A/G]TGATGTGTACTATGT	10116
rs149321811	snp	C/T	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68285299	GTTTCCAGTGTTTGA[C/T]TGTTATGAATAAAAC	10116
rs149585582	snp	A/G	0.00119737	0.0244387	intron-variant	FEM1B	GRCh38.p7	15:68280142	AGAGTTAAGAATTTC[A/G]AAAGGTTTTGCTTAT	10116
rs149621885	snp	G/T	0.00636936	0.0560724	downstream-variant-500B	FEM1B	GRCh38.p7	15:68296344	ATTTCAAATAATGCT[G/T]CAGTCAACATCCTTA	10116
rs149652183	snp	A/G	9.89544e-05	0.00703331	synonymous-codon	FEM1B	GRCh38.p7	15:68291110	AAGTACAACTGGGGT[A/G]TCTGAAATACTGCTT	10116
rs149657294	snp	A/G	0.00676609	0.0577691	utr-variant-5-prime, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68277953	CGGAAAGCGCAGGAG[A/G]AGGCAGTGTTAGGCC	10116
rs149984660	in-del	-/TAAAAAAAAAA			intron-variant	FEM1B	GRCh38.p7	15:68283502	GACCTCATCTCTACC[-/TAAAAAAAAAA]AAAAAAAAAAAAAAA	10116
rs150061886	snp	A/G	0.00279162	0.0372561	intron-variant	FEM1B	GRCh38.p7	15:68287134	GACCTCCGGTGATCC[A/G]CCTGCTTTGGCCTCC	10116
rs150312899	snp	C/T	8.27452e-05	0.00643162	synonymous-codon, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278564	GCAGCGCTCCACGCC[C/T]CTCATCATCGCAGCC	10116
rs150382848	snp	G/T	0.0174175	0.0916809	intron-variant	FEM1B	GRCh38.p7	15:68289144	TTTATTTTTTTCTTC[G/T]TAAAGCAGTGTCTAA	10116
rs150399040	snp	C/T	0.0260105	0.111035	intron-variant	FEM1B	GRCh38.p7	15:68279457	TTTGACCAGAATTGT[C/T]AGGTTTGACATTATC	10116
rs150430252	snp	G/T	0.00597247	0.0543191	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68291748	TTCCATTATTTATAC[G/T]GAGTGATGCAGCACA	10116
rs150452261	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	FEM1B	GRCh38.p7	15:68275891	CCAGGCACTCCTCCA[C/G]GTCAGCTTGTGCCCA	10116
rs150718403	snp	A/G	0.0626037	0.165477	intron-variant	FEM1B	GRCh38.p7	15:68281698	TCTCGGCTCACTGCA[A/G]GCTCTGCCTTCCGGG	10116
rs150748620	snp	G/T	0.000798403	0.0199641	downstream-variant-500B	FEM1B	GRCh38.p7	15:68296043	CCCGCCTCCTATTTG[G/T]ACTCTGCAGAGACAA	10116
rs150749745	in-del	-/TGGATCCCT	0.02016	0.0983543	intron-variant	FEM1B	GRCh38.p7	15:68283559	GGAGGCTGAGGTGGA[-/TGGATCCCT]TGAGCCTGGGAGATC	10116
rs151125509	snp	C/T	0.00350694	0.0417274	synonymous-codon	FEM1B	GRCh38.p7	15:68290183	AAAGACATACCACTA[C/T]CTATATTTAGCCATG	10116
rs151297468	snp	A/T	0.0263992	0.111815	intron-variant	FEM1B	GRCh38.p7	15:68286925	GGAGTTTTGCTCTTG[A/T]CACCCAGGCTGGATT	10116
rs181098440	snp	C/T			intron-variant, utr-variant-5-prime	FEM1B	GRCh38.p7	15:68278941	TAGTCGTCTTCTCTA[C/T]TAGATAGTCTGTGAA	10116
rs181131583	snp	A/G	0.00358779	0.0422022	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68292886	ACAGAAGGGGGGACT[A/G]TCCCCCAAGGATGCA	10116
rs181265233	snp	A/G	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68283928	CTCACTCTTGTTGCC[A/G]AGGCTAAAGTGCAAT	10116
rs181503697	snp	A/C	0.000798403	0.0199641	intron-variant	FEM1B	GRCh38.p7	15:68280575	TTCGAGCTGTGTTTT[A/C]AAGAATAGTAGTAGG	10116
rs181515066	snp	C/G	8.23689e-05	0.00641698	synonymous-codon	FEM1B	GRCh38.p7	15:68290876	CCACACCAATGACGT[C/G]TGCAGCTTTCCAAAT	10116
rs181727460	snp	A/G	0.00159617	0.0282053	intron-variant	FEM1B	GRCh38.p7	15:68282719	GTGCTTCTCCTTTAG[A/G]AACTTAGTAAATACT	10116
rs182017307	snp	C/T	0.00119737	0.0244387	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68294512	CAAGTGAGCAACACC[C/T]TGTTAAGAGTTTTCA	10116
rs182191282	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB	FEM1B	GRCh38.p7	15:68277559	CGCCCCCACTCCCTG[A/G]CTGGAGACCCTCAGG	10116
rs182392610	snp	A/G			intron-variant	FEM1B	GRCh38.p7	15:68281156	CTGAGTACATTAACA[A/G]TAGAAAGCTGACTTG	10116
rs182483704	snp	C/T	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68279720	GGGAAATGTTCTGTT[C/T]CGGTTGATTCTTTTT	10116
rs182567984	snp	G/T			intron-variant	FEM1B	GRCh38.p7	15:68284782	TTGTGGGAGGGACCT[G/T]GTGGGAGGCAACTGA	10116
rs182624883	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	FEM1B	GRCh38.p7	15:68276790	TGTTGCATCCTCTGA[A/C]TTCATCTATCATTCT	10116
rs183055238	snp	A/G	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68281807	ATTTTTAGTAGAGAC[A/G]GTTTCACCGTGTTAG	10116
rs183127866	snp	A/T	0.0023933	0.0345097	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68295289	TGATGAATGGCCTAA[A/T]CAGAAAAGTGAAGGA	10116
rs183268937	snp	A/C	0.00636936	0.0560724	intron-variant	FEM1B	GRCh38.p7	15:68285768	TGAACTCTTAGGTTC[A/C]AACAGTCCTCTTCTT	10116
rs183395662	snp	A/C/T	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68287278	TAGGAGGCTTCTGAT[A/C/T]TTTTCTGAGGTATGT	10116
rs183415859	snp	A/G	0	0	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68295030	ATCTTTAGATGGGCT[A/G]GGTTATACAGCATGC	10116
rs183834847	snp	A/C			intron-variant, utr-variant-5-prime	FEM1B	GRCh38.p7	15:68279102	TTTTTACTCCCTTCA[A/C]GTGAGTGGTTCCGTA	10116
rs184186511	snp	A/G	0.00159617	0.0282053	intron-variant	FEM1B	GRCh38.p7	15:68281229	GAGACACATGGCCAT[A/G]TAGGGATTAACAGCT	10116
rs184318443	snp	G/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	FEM1B	GRCh38.p7	15:68278898	CCCTCTGTGGGAAGA[G/T]AACCACACCCTCGGC	10116
rs184359529	snp	C/T	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68288299	TTATTCTCTTTTCCA[C/T]TTCATGGGGGATATA	10116
rs184597238	snp	C/G	0.00318978	0.0398085	intron-variant	FEM1B	GRCh38.p7	15:68289045	AGGTTTATGTTATCT[C/G]TTCATATTGTGTGTG	10116
rs184644513	snp	G/T	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68282017	AGAAGAAAAGTCACA[G/T]GAGTGGGAATGAAAG	10116
rs185418232	snp	C/T	0.00676609	0.0577691	utr-variant-5-prime, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278251	CGGCCTCCTCTGCGT[C/T]TCCGCCTTCCCTGGG	10116
rs185654481	snp	A/G	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68281072	CCCAGTCATTTTAGG[A/G]TTTTAGAACCAAAAA	10116
rs185842450	snp	C/T	0.00398564	0.0444627	intron-variant	FEM1B	GRCh38.p7	15:68282528	AGGTAATAGATGAGC[C/T]CAGCCTTGTGATCAG	10116
rs185897567	snp	A/T	0.00358779	0.0422022	intron-variant	FEM1B	GRCh38.p7	15:68283823	GATGTGTACTATGTT[A/T]CCTTACGTTTGATGC	10116
rs185901540	snp	A/C	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68284981	CCATGTGGAACTGTA[A/C]GTCCAGTAAACCTCT	10116
rs186023604	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68293525	AAGTAAAACTGTTGA[C/T]TGAAATGCTGACAGG	10116
rs186145707	snp	A/T			intron-variant	FEM1B	GRCh38.p7	15:68281201	ACCTTTGAAAAACAC[A/T]TAGCCAGCACTTGAG	10116
rs186293579	snp	C/T	0.00199481	0.0315187	intron-variant	FEM1B	GRCh38.p7	15:68284676	GCCCCTTCTCAGTTT[C/T]CTCCCTTTCCTTGCC	10116
rs186380567	snp	G/T	0.000798403	0.0199641	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68294618	GGAATGGGGTGGGAT[G/T]AGGAGTGAGTTGCCA	10116
rs186758386	snp	C/T	0.000399281	0.0141238	synonymous-codon	FEM1B	GRCh38.p7	15:68291155	GATGAGTCTCAAGTG[C/T]CTGGCTGCCCGAGCA	10116
rs186938560	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	FEM1B	GRCh38.p7	15:68276877	ACTGTTCCCTCCTCA[C/G]GACTTTTATATTAGC	10116
rs187037405	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	FEM1B	GRCh38.p7	15:68276197	CAGAGACGCTACCAG[C/T]AGAATCTTACCTTCA	10116
rs187090777	snp	C/T	0.000798403	0.0199641	intron-variant	FEM1B	GRCh38.p7	15:68280049	GAAGTCATTGAGATA[C/T]GAATTTCTGTAATAA	10116
rs187389448	snp	C/T	0.0023933	0.0345097	intron-variant	FEM1B	GRCh38.p7	15:68281871	CGCATGCCTCGGCCT[C/T]CCTAAGTGCTGGGAT	10116
rs187440823	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	FEM1B	GRCh38.p7	15:68277709	CCGGTCGGCTTAGGC[A/G]GAGACACCCCACTTA	10116
rs187600233	snp	C/T	0.00597247	0.0543191	intron-variant	FEM1B	GRCh38.p7	15:68286259	ATATTATTCTGTCCC[C/T]GTGCCAGCACTTATT	10116
rs187936808	snp	A/G			intron-variant	FEM1B	GRCh38.p7	15:68287533	TTAAATTATTATAAA[A/G]TGAGTATTTTCAGTA	10116
rs187983708	snp	G/T	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68288490	AATCTACTTATCAGG[G/T]CTTTTGGTTAGTGGT	10116
rs188467310	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68295231	TGTGTATAGGGGTAA[A/G]TATTGCTAAATTATT	10116
rs188667388	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	FEM1B	GRCh38.p7	15:68278917	CACACCCTCGGCCTT[C/G]AAATCTAATAGTCGT	10116
rs188742753	snp	G/T	0.00279162	0.0372561	intron-variant	FEM1B	GRCh38.p7	15:68281252	TAACAGCTGTGTGCT[G/T]AAGTAGATTAGTGTT	10116
rs188776003	snp	A/G	0.00279162	0.0372561	utr-variant-5-prime, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278271	CCTTCCCTGGGCCGC[A/G]CTGCTGCCTGGGCGC	10116
rs188804247	snp	C/G/T	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68283830	ACTATGTTTCCTTAC[C/G/T]TTTGATGCATTTTAT	10116
rs189046576	snp	A/G	0.000798403	0.0199641	intron-variant	FEM1B	GRCh38.p7	15:68279332	ATCTTATCCCGTGAT[A/G]TTGTGGGGAAGCTTG	10116
rs189074615	snp	C/T	0.00119737	0.0244387	intron-variant	FEM1B	GRCh38.p7	15:68289466	GCTTTCCTTAAATTA[C/T]CTGTTTTTATTTTCA	10116
rs189559613	snp	C/G	0.00199481	0.0315187	intron-variant	FEM1B	GRCh38.p7	15:68282104	ACAGAACAAGGGGGA[C/G]GTGTCATATGACCAT	10116
rs189587944	snp	A/G			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68292191	TAAGGTATTTTACTT[A/G]TGACAGATGAAAAGG	10116
rs189745872	snp	A/G	0.0023933	0.0345097	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68293582	AATAAACTATGAACT[A/G]TGCTAATGGTAATTA	10116
rs189865537	snp	A/C	0.000798403	0.0199641	upstream-variant-2KB	FEM1B	GRCh38.p7	15:68277032	ACCAGTTCAACTGAT[A/C]TTGTCTATCATTTGT	10116
rs190113480	snp	G/T	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68281150	GTTAGCCTGAGTACA[G/T]TAACAATAGAAAGCT	10116
rs190363701	snp	A/T	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68282558	GAAATGTTATCTCTT[A/T]TTGTGAAAAGTTTCC	10116
rs190698288	snp	A/C	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68281225	ACTTGAGACACATGG[A/C]CATATAGGGATTAAC	10116
rs190785049	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68294739	AGATTTTCTGTAAGA[A/G]TCTTAAATGTTCCTT	10116
rs191080336	snp	A/C	0.000798403	0.0199641	intron-variant	FEM1B	GRCh38.p7	15:68285471	CAACCAAATTACATT[A/C]CTACTTGCAGTTTCC	10116
rs191189698	snp	C/T	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68284763	TATCTTGAATTCCCA[C/T]GTGTTGTGGGAGGGA	10116
rs191460155	snp	A/T	0.000798403	0.0199641	upstream-variant-2KB	FEM1B	GRCh38.p7	15:68276757	ACCCTTTGCTATGGG[A/T]TATTAGGCCCTAACG	10116
rs191843768	snp	C/T	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68281909	TTGAGCCACTGTGCG[C/T]GGCCTCTTGTTCACA	10116
rs192013868	snp	A/G	0.000798403	0.0199641	intron-variant	FEM1B	GRCh38.p7	15:68280264	GGCTTATCTTGCCCA[A/G]TGTTCTGTACTGGCC	10116
rs192081746	snp	A/G	0.00438332	0.0466095	intron-variant	FEM1B	GRCh38.p7	15:68286672	AGTTTTCAGTGTAGA[A/G]GTCTTGTGCATTTTT	10116
rs192340158	snp	A/C	0.0185938	0.0946107	intron-variant	FEM1B	GRCh38.p7	15:68281692	GCGCGATCTCGGCTC[A/C]CTGCAAGCTCTGCCT	10116
rs192563532	snp	C/T	0.00159617	0.0282053	intron-variant	FEM1B	GRCh38.p7	15:68288820	TAAATTGGAGCATAA[C/T]GTAACTTAGAGAAAA	10116
rs192804259	snp	C/G	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68288141	GGCCTAACGCCTCTT[C/G]TGTGTGGTCCTTAAT	10116
rs192875500	snp	C/G	0.000798403	0.0199641	intron-variant, utr-variant-5-prime	FEM1B	GRCh38.p7	15:68278856	CCATGTTTTGCTGCC[C/G]GTCCTCATCAGCCCC	10116
rs193261445	snp	A/G	0.00835141	0.0640778	utr-variant-5-prime, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68277955	GAAAGCGCAGGAGGA[A/G]GCAGTGTTAGGCCTT	10116
rs199597830	snp	A/G	6.65757e-05	0.00576918	missense	FEM1B	GRCh38.p7	15:68291175	CTGCCCGAGCAGTTC[A/G]GGCTAATGACATTAA	10116
rs199702117	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68293802	ACCCTTCCCCAACTT[A/C]ATTTTTTTTTAAAAA	10116
rs199722163	snp	A/G	3.31791e-05	0.00407289	missense, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278526	ATCCGCTATCTGCTT[A/G]GCTATGTCAGCCAGC	10116
rs199906667	snp	A/G	1.65636e-05	0.00287776	synonymous-codon, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278546	TGTCAGCCAGCAGGG[A/G]GGGCAGCGCTCCACG	10116
rs199942439	in-del	-/AGGAA	0.029116	0.117091	intron-variant	FEM1B	GRCh38.p7	15:68285274	TTCCTATTAATTAAT[-/AGGAA]ATTTTGGTTGTTTCC	10116
rs199982589	snp	A/G	0.00199792	0.0315431	missense	FEM1B	GRCh38.p7	15:68290397	GATGTTTCTCATCCC[A/G]TCATTTACAGAGGAG	10116
rs200277973	in-del	-/ACTATT	0.00279162	0.0372561	downstream-variant-500B	FEM1B	GRCh38.p7	15:68296061	TCTGCAGAGACAATC[-/ACTATT]AATAGTTTTTTGAGT	10116
rs200618455	snp	C/G	0.00199804	0.0315441	intron-variant, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278683	AGGTACATCCCAAGC[C/G]AGCCTCTCTCCGACG	10116
rs200723170	in-del	-/C			intron-variant	FEM1B	GRCh38.p7	15:68286800	ACAATAAAAACATAA[-/C]AAAAAAATAACAAAA	10116
rs200735664	snp	A/G	2.6355e-05	0.00362999	utr-variant-5-prime, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278395	CGGTGGCGACCAAAC[A/G]GGTGTTGGAGTTGGC	10116
rs200910706	snp	A/G	0.00199792	0.0315431	missense	FEM1B	GRCh38.p7	15:68290869	ATGATTTCCACACCA[A/G]TGACGTCTGCAGCTT	10116
rs201133680	snp	A/C	0.00168186	0.02895	missense	FEM1B	GRCh38.p7	15:68290560	TACATTTGAATGAAA[A/C]TGTGAAGGCCCCAGA	10116
rs201268065	snp	A/G	0.00199798	0.0315436	missense	FEM1B	GRCh38.p7	15:68291141	AAAACTCAAATGAAG[A/G]TGAGTCTCAAGTGCC	10116
rs201342450	snp	C/T			upstream-variant-2KB	FEM1B	GRCh38.p7	15:68276443	GAGCCGAGCCCAGTC[C/T]CTTGGAGCCACATAA	10116
rs201703543	snp	C/G	0.000428597	0.0146327	synonymous-codon, utr-variant-5-prime	FEM1B	GRCh38.p7	15:68289727	AGTAACTAATTCAAC[C/G]CCCCTGCGGGCAGCA	10116
rs201888200	snp	C/T			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68291862	AAATTTAAATCCATT[C/T]GAAATTGTTGCATTA	10116
rs367665442	snp	A/G	5.74707e-05	0.00536023	intron-variant	FEM1B	GRCh38.p7	15:68289582	TGGCCTCTGTTATCT[A/G]ACTGCTTATTCTTTT	10116
rs367887087	snp	A/G			missense	FEM1B	GRCh38.p7	15:68290154	GCAAATGACCGTGAG[A/G]ACTATGACATCATAA	10116
rs367982979	snp	A/G	0.000798403	0.0199641	intron-variant	FEM1B	GRCh38.p7	15:68289513	ATTAATGTTCTGGAG[A/G]GTGAGGTCTTGGTCG	10116
rs368055837	in-del	-/TCTT	0.00478085	0.0486577	downstream-variant-500B	FEM1B	GRCh38.p7	15:68296200	TTTTCATGTAATATA[-/TCTT]AGGCATTTTCCATTT	10116
rs368263455	snp	C/T			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68291603	TATTTCTGTTAAGCC[C/T]ATGTCAGCATGTTAT	10116
rs368375615	snp	A/C			intron-variant	FEM1B	GRCh38.p7	15:68279160	ATGTCAAAATAAGCA[A/C]CTAGAACCAGCAGCA	10116
rs368483635	snp	C/G			utr-variant-5-prime, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278331	GCTGTGAGGGCCCAG[C/G]TTTAAAGCGCTGGCG	10116
rs368492318	snp	C/T			intron-variant	FEM1B	GRCh38.p7	15:68288624	CACATATCAGATGTT[C/T]AGTAAGTAAGTGATA	10116
rs368864440	in-del	-/ATAA			intron-variant	FEM1B	GRCh38.p7	15:68286807	AAACATAACAAAAAA[-/ATAA]CAAAAGTGAATTTTA	10116
rs368926800	snp	A/C/G	9.89355e-05	0.00703271	missense	FEM1B	GRCh38.p7	15:68290488	ACCTCAGACAAAAAG[A/C/G]TAACAGGAACACCCA	10116
rs369015177	snp	A/G			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68292913	TGCAAGATACTTTTT[A/G]CAGTTGCTATCATTA	10116
rs369702955	snp	C/T	5.65979e-05	0.00531937	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68291262	CTGGATATGTAAAGT[C/T]GTTTAATGTGGTGCT	10116
rs369816669	snp	A/T			intron-variant	FEM1B	GRCh38.p7	15:68280394	CTTTTGTCTTGGAGG[A/T]TGTCAGTCTGGGTGG	10116
rs369902682	in-del	-/ATTCA			intron-variant	FEM1B	GRCh38.p7	15:68285976	TGTGATCAACACTAA[-/ATTCA]TTAAGAATAGTCTAT	10116
rs369950571	snp	G/T	1.64936e-05	0.00287168	missense	FEM1B	GRCh38.p7	15:68290207	AGCCATGTTAGAGAG[G/T]TTCCAAGATGGTGAT	10116
rs370211339	snp	A/G			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68295354	CAAGATTTTGTATCT[A/G]TTTTTTATCAGGTGT	10116
rs370392761	snp	A/G			intron-variant	FEM1B	GRCh38.p7	15:68287623	TATATGTCTTAGTCT[A/G]TTCTGTGGTGTTATA	10116
rs370707411	snp	C/G/T	1.65542e-05	0.00287695	missense, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278557	AGGGAGGGCAGCGCT[C/G/T]CACGCCCCTCATCAT	10116
rs370712020	in-del	-/G			intron-variant	FEM1B	GRCh38.p7	15:68279675	GCTAAAACTCGACTG[-/G]AAAAAAACATTTCTT	10116
rs371104171	snp	C/T			upstream-variant-2KB	FEM1B	GRCh38.p7	15:68277730	ACCCCACTTAGCGTC[C/T]CTCCCGCTCCCGCCC	10116
rs371110892	in-del	-/ATC			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68294312	CCAAAGCAGACCATC[-/ATC]TGTAAGCTTTGGTCT	10116
rs371369808	snp	A/T			intron-variant	FEM1B	GRCh38.p7	15:68289544	GTGGGAGTGAATACA[A/T]CCCTTAAACATATGT	10116
rs371468348	in-del	-/T			intron-variant	FEM1B	GRCh38.p7	15:68286217	AATCTATTTCTGGAG[-/T]TTTTTTTTTTTTTTG	10116
rs371578342	snp	C/T			intron-variant	FEM1B	GRCh38.p7	15:68287830	ACGTTGCTAACGTCT[C/T]TTTTTTTTTTTTTTT	10116
rs371624753	snp	C/G	0.000153988	0.00877328	missense	FEM1B	GRCh38.p7	15:68290918	AAAGCTCCTGCTGGA[C/G]TGTGGTGCTGAGGTG	10116
rs371697589	in-del	-/GTTT			intron-variant	FEM1B	GRCh38.p7	15:68284512	TTTTTAATTATATCT[-/GTTT]TTTTAGTGGAGGTAT	10116
rs371858178	snp	A/C	0.00119737	0.0244387	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68291838	ATTTAATAATAGTTA[A/C]AAATTTATAAATTTA	10116
rs372215057	snp	C/T	0.000153988	0.00877328	intron-variant	FEM1B	GRCh38.p7	15:68289602	CTTATTCTTTTCATG[C/T]GTAGGTATGTCATTG	10116
rs372323856	snp	A/T	1.64977e-05	0.00287203	synonymous-codon	FEM1B	GRCh38.p7	15:68289994	AAAATGGCGTGCTGC[A/T]ATAGTAGTGAATGGC	10116
rs372561452	snp	G/T	4.45147e-05	0.00471756	utr-variant-5-prime, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278415	TTGGAGTTGGCGGCG[G/T]CCATGGAGGGCCTGG	10116
rs372786121	snp	C/T	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68281142	GTGAAAATGTTAGCC[C/T]GAGTACATTAACAAT	10116
rs373504463	snp	A/G	1.65002e-05	0.00287225	missense	FEM1B	GRCh38.p7	15:68290622	GAAATAGAACAAAGT[A/G]TGAACAGAGTGAAAA	10116
rs373528730	in-del	-/T	0.00676609	0.0577691	utr-variant-5-prime, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278280	GGCCGCACTGCTGCC[-/T]GGGCGCGGCGGCGGC	10116
rs373579495	snp	C/G			intron-variant	FEM1B	GRCh38.p7	15:68280563	GAGGAGGTGACGTTC[C/G]AGCTGTGTTTTAAAG	10116
rs373696952	snp	C/T			intron-variant	FEM1B	GRCh38.p7	15:68286110	TCCATATAGATTATC[C/T]TGTTGCTCCATAACT	10116
rs373808088	snp	C/T			downstream-variant-500B	FEM1B	GRCh38.p7	15:68296165	CTTCTACCTTTGCAA[C/T]GCTATTCTGTATCTT	10116
rs373846418	snp	A/G/T	6.03662e-05	0.00549364	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68291290	GCTAAAAAGTAAAGG[A/G/T]CTTTTAATCACAGAC	10116
rs374091554	in-del	-/A			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68292064	TTTCTTATGAAACAA[-/A]TTGTCACAGTGTAGT	10116
rs374112768	snp	A/G			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68293919	TTGATGTTTACTATT[A/G]GTATACTTATGCTTT	10116
rs374147985	in-del	-/TTTG	0.00676609	0.0577691	intron-variant	FEM1B	GRCh38.p7	15:68288880	CACAAAGTGAACATA[-/TTTG]TTTACTAGAGTCCCC	10116
rs374305651	in-del	-/GATCCCTTG			intron-variant	FEM1B	GRCh38.p7	15:68283561	AGGCTGAGGTGGATG[-/GATCCCTTG]AGCCTGGGAGATCTA	10116
rs374555915	in-del	-/AAA	0.0543475	0.155628	intron-variant	FEM1B	GRCh38.p7	15:68287208	ATTCATTCTTTAGTT[-/AAA]AAAAATCAATTAACA	10116
rs374580566	snp	C/T	0.000153988	0.00877328	synonymous-codon	FEM1B	GRCh38.p7	15:68291194	TAATGACATTAACTA[C/T]CAAGACCAGATCCCC	10116
rs374607196	snp	A/T			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68294363	GTTTTATTTCATTAT[A/T]CTAATAGTGGACTAA	10116
rs374653124	snp	A/C	5.01333e-05	0.00500641	intron-variant, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278694	AAGCCAGCCTCTCTC[A/C]GACGCGCGCGGACTC	10116
rs374792610	snp	C/T			utr-variant-5-prime, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278169	CCGGCGCCTGGGACC[C/T]GGCGGGCGGCCCTGA	10116
rs375126766	snp	A/G			intron-variant	FEM1B	GRCh38.p7	15:68281987	GAATACCATGTTGAT[A/G]TAGATGAGTGGACAA	10116
rs375170532	snp	C/T	6.6024e-05	0.00574523	synonymous-codon, utr-variant-5-prime	FEM1B	GRCh38.p7	15:68289796	TGAAAATAATGCCAA[C/T]ATCAGCATTGCCAAC	10116
rs375373890	snp	A/C	0.000319766	0.0126404	utr-variant-5-prime, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278413	TGTTGGAGTTGGCGG[A/C]GGCCATGGAGGGCCT	10116
rs375513455	in-del	-/GATTT			intron-variant	FEM1B	GRCh38.p7	15:68286693	GTGCATTTTTCATTA[-/GATTT]ATTACTATTTATTGG	10116
rs375876991	snp	A/G	3.29995e-05	0.00406185	synonymous-codon	FEM1B	GRCh38.p7	15:68290540	TCAAGTTTTCTCACA[A/G]ATGATACATTTGAAT	10116
rs375920632	snp	A/G	1.64901e-05	0.00287137	missense	FEM1B	GRCh38.p7	15:68290091	TCTCATGCTGATTGC[A/G]ACCGAAGAAGTCGGA	10116
rs375949403	snp	A/G	8.24151e-05	0.00641878	synonymous-codon	FEM1B	GRCh38.p7	15:68290423	AGGAGCTGTTTATGC[A/G]GATAATATGGAATTT	10116
rs376014855	snp	C/T			intron-variant	FEM1B	GRCh38.p7	15:68288275	ATTCAAACTATAGCA[C/T]CAGGAGCATTATTCT	10116
rs376135215	snp	A/G			upstream-variant-2KB	FEM1B	GRCh38.p7	15:68277793	TTCCTCCCCGCCCAA[A/G]TTCCGGCGCCGCTCT	10116
rs376316886	snp	C/T	0.000153988	0.00877328	synonymous-codon, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278516	TGAAAGCGACATCCG[C/T]TATCTGCTTGGCTAT	10116
rs376504470	snp	C/T			upstream-variant-2KB	FEM1B	GRCh38.p7	15:68276883	CCCTCCTCAGGACTT[C/T]TATATTAGCTGTCCC	10116
rs376526441	in-del	-/GTTT			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68293613	ATTTTTTGTTTGTTT[-/GTTT]AGTATAGTGGTAAAT	10116
rs376663504	snp	C/T			upstream-variant-2KB	FEM1B	GRCh38.p7	15:68275953	AGGGTGGTAGGGAGA[C/T]GGAGTTAGAGATATG	10116
rs376986851	snp	A/T	1.65007e-05	0.00287229	missense	FEM1B	GRCh38.p7	15:68290623	AAATAGAACAAAGTA[A/T]GAACAGAGTGAAAAA	10116
rs377002244	in-del	-/T			intron-variant	FEM1B	GRCh38.p7	15:68288729	TGTTAGTATTTTTTT[-/T]CCTGTAGTGGTTGAT	10116
rs377014502	in-del	-/GTT			intron-variant	FEM1B	GRCh38.p7	15:68282262	TTTTTGTTGAGTGTT[-/GTT]CTTTTAAAGTCAGTG	10116
rs377070193	in-del	-/GTT			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68293604	GGTAATTAGATTTTT[-/GTT]TGTTTGTTTAGTATA	10116
rs377458193	snp	C/G	0.00091891	0.0214152	intron-variant, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278698	CAGCCTCTCTCCGAC[C/G]CGCGCGGACTCGTTA	10116
rs398027774	in-del	-/AT/TG	0.00199481	0.0315187	intron-variant	FEM1B	GRCh38.p7	15:68286498	AGGTTGTGTGGTATA[-/AT/TG]TGTGTGTGTGTGTGT	10116
rs398057788	in-del	-/TGTTT			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68291522	AGATATAAAATGTTT[-/TGTTT]ATGTAACAAGGGACA	10116
rs527318681	snp	C/T	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68285263	CAGTTTATCCATTTC[C/T]TATTAATTAATATTT	10116
rs527528532	snp	A/C/G	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68279277	GGCTACTAAGATGGC[A/C/G]TTGGACCTGATGTGG	10116
rs527641349	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	FEM1B	GRCh38.p7	15:68276839	TGCAGCCACACTGAC[A/C]TTTCTGTTTCCGAGC	10116
rs528063212	in-del	-/A	0.00119737	0.0244387	intron-variant	FEM1B	GRCh38.p7	15:68286801	CAATAAAAACATAAC[-/A]AAAAAATAACAAAAG	10116
rs528591880	snp	A/G	0.000798403	0.0199641	downstream-variant-500B	FEM1B	GRCh38.p7	15:68295976	TGGGAAAAAATTCAC[A/G]TAGTAAAGAAAAATT	10116
rs528801476	snp	C/T	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68288188	GGAGCCCTCATGACC[C/T]AATCACCTCTTCAAG	10116
rs528821401	snp	A/G	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68287226	AAAAATCAATTAACA[A/G]ATGCATTTTTAAAAA	10116
rs528826990	in-del	-/TTA	0.00318978	0.0398085	intron-variant	FEM1B	GRCh38.p7	15:68285528	CATCTTGCTCAACAC[-/TTA]TTATTGCCCTGTCAG	10116
rs528996153	snp	C/T			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68295038	ATGGGCTGGGTTATA[C/T]AGCATGCCCTCCCCC	10116
rs529881834	snp	C/G			intron-variant, utr-variant-5-prime	FEM1B	GRCh38.p7	15:68279025	GGTGATGTAACTGAT[C/G]AGAAATTAAGGAGGT	10116
rs529918869	in-del	-/AGGGAGGAAG			upstream-variant-2KB	FEM1B	GRCh38.p7	15:68276502	TTTGTCCTTTGGGGA[-/AGGGAGGAAG]AGGGAGGAAGTCACT	10116
rs530038726	snp	A/T			intron-variant	FEM1B	GRCh38.p7	15:68284415	ACTTGAAATTGAAAT[A/T]ACTTGAAATGAAAGT	10116
rs530239331	snp	C/G	0.00318978	0.0398085	intron-variant	FEM1B	GRCh38.p7	15:68288912	CCTTTGTGCTTTCTC[C/G]CATTTCACTACCTCT	10116
rs530280385	snp	C/T	0.00119737	0.0244387	intron-variant	FEM1B	GRCh38.p7	15:68281728	GTTCATGCCATTCTC[C/T]TGCCTCAGCCTCCCG	10116
rs530727510	snp	A/T	1.6546e-05	0.00287624	missense	FEM1B	GRCh38.p7	15:68289956	GCTGAAGCTGGGCAC[A/T]TAGATATTGTGAAAG	10116
rs531079088	snp	A/T	0.00119737	0.0244387	intron-variant	FEM1B	GRCh38.p7	15:68288265	GTGGGAACACATTCA[A/T]ACTATAGCACCAGGA	10116
rs531169881	snp	C/T	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68288805	ACATTTTAAAACTTT[C/T]AAATTGGAGCATAAC	10116
rs531484880	snp	A/C/T	3.38921e-05	0.00411645	intron-variant, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278674	TCGACGGGTAGGTAC[A/C/T]TCCCAAGCCAGCCTC	10116
rs531550559	snp	C/T	8.25035e-05	0.00642222	synonymous-codon	FEM1B	GRCh38.p7	15:68290589	GACATAGAATGTGTT[C/T]TGAGATGCAGTGTTT	10116
rs531574868	snp	C/G	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68285759	GGCTGGTCTTGAACT[C/G]TTAGGTTCAAACAGT	10116
rs531771199	snp	C/G	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68283426	CCCAGCACTTTGGGA[C/G]GCCTAGGTGGGGATA	10116
rs531775362	snp	C/G	0.00159617	0.0282053	upstream-variant-2KB	FEM1B	GRCh38.p7	15:68277462	CCTTCCCTAACCCCG[C/G]CTCAGGGGCAGAAGC	10116
rs532498635	snp	C/T			intron-variant	FEM1B	GRCh38.p7	15:68279276	TGGCTACTAAGATGG[C/T]ATTGGACCTGATGTG	10116
rs532571603	snp	A/G	0.000330077	0.0128425	missense, utr-variant-5-prime	FEM1B	GRCh38.p7	15:68289797	GAAAATAATGCCAAC[A/G]TCAGCATTGCCAACA	10116
rs532712613	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	FEM1B	GRCh38.p7	15:68275815	GGTTCGGAATAGAAT[A/G]TAGAATGATTCAGGA	10116
rs532800904	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB	FEM1B	GRCh38.p7	15:68276718	TAAAACCCTTCAAAT[A/G]CCCCCATCACAGAGT	10116
rs533141310	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278132	GGGCGGCGTCCGCCA[C/T]GGAGATCCCCTCGGT	10116
rs533334475	snp	A/G			intron-variant	FEM1B	GRCh38.p7	15:68281735	CCATTCTCCTGCCTC[A/G]GCCTCCCGAGTAGCT	10116
rs533764155	snp	A/G	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68284580	AATACTGTACAATGA[A/G]TTTTTAATATGTTTA	10116
rs533893343	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278270	GCCTTCCCTGGGCCG[C/T]ACTGCTGCCTGGGCG	10116
rs534338022	snp	A/G			intron-variant	FEM1B	GRCh38.p7	15:68280116	ATAAGGGAGAATAGT[A/G]GGGAGAAAAAAGAGT	10116
rs534474219	snp	A/G	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68283547	AGGTAGTATGCAGGA[A/G]GCTGAGGTGGATGGA	10116
rs534545592	snp	C/T	0.00119737	0.0244387	intron-variant	FEM1B	GRCh38.p7	15:68287857	TTTTTTTTTTTGAGA[C/T]GAAGTTTTGCTCTGT	10116
rs534739900	snp	A/T	0.00398564	0.0444627	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68295024	GCCCAAATCTTTAGA[A/T]GGGCTGGGTTATACA	10116
rs534824801	snp	A/G	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68286181	GAGCCTTTGTCAGAA[A/G]TCAAGGGATTCTGTA	10116
rs534920624	snp	C/T	0.00358779	0.0422022	intron-variant	FEM1B	GRCh38.p7	15:68279518	TTTTACAGATTACAA[C/T]TGTATAACGATTTTG	10116
rs535282205	snp	C/T	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68288791	ACACATATACATATA[C/T]ATTTTAAAACTTTTA	10116
rs535537431	in-del	-/GAA	0.00119737	0.0244387	upstream-variant-2KB	FEM1B	GRCh38.p7	15:68277340	TCAGGCCGTACTTCC[-/GAA]AGTCCCTTCTCAGAG	10116
rs535565071	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68293929	CTATTGGTATACTTA[C/T]GCTTTGAATTGTAAA	10116
rs535573040	snp	C/G			intron-variant	FEM1B	GRCh38.p7	15:68285093	TTAGTTTTGCCTGTA[C/G]TTGAACTTCCTATAA	10116
rs535686928	snp	G/T	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68285933	CGGTTAATGCTTTTT[G/T]TTTTTTTTGGTATTC	10116
rs536032790	snp	A/G	0.00438332	0.0466095	intron-variant	FEM1B	GRCh38.p7	15:68281908	CTTGAGCCACTGTGC[A/G]CGGCCTCTTGTTCAC	10116
rs536045767	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68294767	CTTTTCAAATTAGAT[A/G]TGTTGATGCACACAT	10116
rs536075003	snp	A/C	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68282657	ATACATAATAGAGAA[A/C]TTGCATTGTAATTTT	10116
rs536423687	snp	C/G			intron-variant	FEM1B	GRCh38.p7	15:68279608	TTTTGAAGTCAGTAG[C/G]GTCTGAGCATAAAAA	10116
rs536461256	snp	A/G			utr-variant-5-prime, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278021	TCTTTCGCCATCCGG[A/G]GTGCGCGAGGTCCTC	10116
rs536645569	snp	C/T	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68287748	TTGTCTGGTGAGGGC[C/T]GCATCCTCCAGAGGG	10116
rs536959924	snp	A/G	0.00159617	0.0282053	upstream-variant-2KB	FEM1B	GRCh38.p7	15:68276887	CCTCAGGACTTTTAT[A/G]TTAGCTGTCCCCTTT	10116
rs537164233	snp	C/T	0.00159617	0.0282053	intron-variant	FEM1B	GRCh38.p7	15:68279592	TAGCATTTTTTTTTT[C/T]TTTTGAAGTCAGTAG	10116
rs537431383	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	FEM1B	GRCh38.p7	15:68296166	TTCTACCTTTGCAAC[A/G]CTATTCTGTATCTTA	10116
rs537468147	snp	C/T	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68286838	TTAATTAAACTGAAT[C/T]GTTTGCAAAACATAT	10116
rs537602216	snp	A/G	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68280527	CTGTTTTATCCGGGG[A/G]GAATCTAGAAAGGCT	10116
rs537674605	snp	A/G			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68295555	TGCAATCCTCCGTGC[A/G]GAGGAACTACACTGT	10116
rs537839159	snp	A/G	7.301e-05	0.0060415	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68291249	TTTCATTAAGTGACT[A/G]GATATGTAAAGTCGT	10116
rs537891920	snp	A/G	0.00159617	0.0282053	upstream-variant-2KB	FEM1B	GRCh38.p7	15:68275930	AAGTGTGTTGGCAGA[A/G]GAGAGGGAGGGTGGT	10116
rs537962085	snp	C/G	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68284512	TTTTTAATTATATCT[C/G]TTTTTTTAGTGGAGG	10116
rs538550896	snp	C/T	1.64874e-05	0.00287113	synonymous-codon	FEM1B	GRCh38.p7	15:68290258	TCTTCCACCAATCCA[C/T]GCTTATGGGAATAGA	10116
rs538744576	snp	C/T	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68282724	TCTCCTTTAGGAACT[C/T]AGTAAATACTGCATT	10116
rs539614764	in-del	-/TTTTA			intron-variant	FEM1B	GRCh38.p7	15:68286004	AGTCTATGGCTTTTT[-/TTTTA]TTTTGAGAAGCTTTT	10116
rs539635279	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68292605	ATGCCTTAGCTACTC[A/G]TAGTGCATGGTACTG	10116
rs539673018	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68293874	TCTGTGAACTCTAGG[C/G]TGTCTCCATTTTGCA	10116
rs539732677	in-del	-/ATTT	0.00119737	0.0244387	intron-variant	FEM1B	GRCh38.p7	15:68287673	AATTTATGAACAGAA[-/ATTT]ATTTCTCATATTTCT	10116
rs539746007	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68295169	CTTTGTGTTAATGTG[C/T]AGGGAAGAGACAGTG	10116
rs539758509	snp	C/T	0.00119737	0.0244387	intron-variant	FEM1B	GRCh38.p7	15:68285373	TAGTTATCTGGTATA[C/T]ATCAAGGAGTGGAAT	10116
rs540487830	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68292085	ACAGTGTAGTTATAC[A/G]TTCTATTTTTGTCCC	10116
rs540735559	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68295606	TGATTTATAACAAAC[C/T]GGTGATGTCATTCTA	10116
rs540774270	snp	A/T	0.00119737	0.0244387	intron-variant	FEM1B	GRCh38.p7	15:68286444	TGCAGTGGCCTGATC[A/T]TGGCTCATTGTAGCC	10116
rs540820618	snp	A/C	0.0023933	0.0345097	intron-variant	FEM1B	GRCh38.p7	15:68282292	GTGCTAGTACTAATA[A/C]TTCTGATAAATGTTG	10116
rs540859120	snp	C/T	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68283078	GGAAAAAAATGGAAA[C/T]TATTAGACTATACCA	10116
rs541060550	snp	A/T	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68284821	AGCAGGTCTTTCCCG[A/T]GCTGTTCTCTTGATA	10116
rs541211412	snp	C/T	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68287110	TGGCCAGGTTGGTCT[C/T]GAACTCCTGACCTCC	10116
rs541231283	in-del	-/AACTTAATTTTTTTTTAAAA	0.00199481	0.0315187	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68293797	GCCAGACCCTTCCCC[-/AACTTAATTTTTTTTTAAAA]AAGGAAAATAGGTAA	10116
rs541257984	snp	C/G	0.000798403	0.0199641	intron-variant	FEM1B	GRCh38.p7	15:68279990	AAGGAGTGAAGCACA[C/G]TGACCTCTGAACCTC	10116
rs541406783	snp	C/T			intron-variant	FEM1B	GRCh38.p7	15:68284242	ATTATAACTATAATA[C/T]AATAGTATAATAGGG	10116
rs541445935	snp	G/T	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68285583	GCTGGGTGTGTATAT[G/T]GGTAAACTGGTTTTA	10116
rs541605631	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68294440	AAAATATGATTTGGG[A/G]GCAGCAGCTTTCTAA	10116
rs541673808	snp	A/G			intron-variant	FEM1B	GRCh38.p7	15:68286689	TCTTGTGCATTTTTC[A/G]TTAGATTTATTACTA	10116
rs541805946	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68291848	AGTTACAAATTTATA[A/G]ATTTAAATCCATTTG	10116
rs541891846	snp	C/T	0.000798403	0.0199641	intron-variant	FEM1B	GRCh38.p7	15:68284084	GAGATGGGGTTTTTC[C/T]GTGTTGGTCAGGCTG	10116
rs541893848	snp	A/G/T	0.000399281	0.0141238	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68292878	GGGAGGGGACAGAAG[A/G/T]GGGGACTATCCCCCA	10116
rs542115998	snp	C/T	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68286383	TTCTTTCTTTCTCTC[C/T]TTCCCATTTTAGAGA	10116
rs542152350	snp	C/T	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68279267	TAGATATATTGGCTA[C/T]TAAGATGGCATTGGA	10116
rs542316480	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	FEM1B	GRCh38.p7	15:68277492	CAGGACCCGCACCGT[C/T]TATAGTAAAATAGGG	10116
rs542324030	snp	C/G	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68281524	TCTACCTAAAACCTT[C/G]TATAATACCTTAGGA	10116
rs542327301	snp	A/G	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68288643	AAGTAAGTGATAAGT[A/G]TGAAGCCACAAGTCC	10116
rs542430000	in-del	-/T			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68293803	CCTTCCCCAACTTAA[-/T]TTTTTTTTTAAAAAA	10116
rs543037725	snp	A/G	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68279830	TAGCCCATGGGCAAT[A/G]GCTTATATCACGGGT	10116
rs543124225	snp	A/G	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68288011	ATTTCTGTATTTTTG[A/G]TAGAGATGGGGTTTC	10116
rs543409514	snp	C/T			intron-variant	FEM1B	GRCh38.p7	15:68289225	TTGCTACCTGGAGGC[C/T]ACTGGGAAGGAGGAA	10116
rs543441950	snp	A/G	1.66203e-05	0.00288268	missense, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278649	ACTCAGCAGACTGGC[A/G]CCGTCCGCTTCGACG	10116
rs543753099	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68295816	TAACAATCTTGCTGT[A/G]TAAAAGGAAAAAATG	10116
rs543904533	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	FEM1B	GRCh38.p7	15:68276537	TCACTTTCATATTGA[G/T]TTTTTTGAGACTGTC	10116
rs544224515	snp	C/T	0.00119737	0.0244387	intron-variant	FEM1B	GRCh38.p7	15:68282950	ACCAGTCTTGTGAAA[C/T]ATTCTGCATTGAATT	10116
rs544553519	snp	C/T	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68281707	ACTGCAAGCTCTGCC[C/T]TCCGGGTTCATGCCA	10116
rs544600450	snp	C/T			synonymous-codon, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278525	CATCCGCTATCTGCT[C/T]GGCTATGTCAGCCAG	10116
rs544892664	snp	A/G	4.95381e-05	0.0049766	missense, utr-variant-5-prime	FEM1B	GRCh38.p7	15:68289672	ATTTTGAAGTTGTTA[A/G]ACTTCTAGTCAGCCA	10116
rs544901777	snp	A/G	0.000798403	0.0199641	intron-variant	FEM1B	GRCh38.p7	15:68282164	GTCTGACTGCTCTCT[A/G]CCAGAGTTTGTGGAG	10116
rs544977424	snp	C/T	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68281659	GTCTCGCTCTGTCGC[C/T]GGGGCTGGAGTGCAG	10116
rs545342206	snp	A/C	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68288205	ATCACCTCTTCAAGA[A/C]ATCACCTCTTAATGC	10116
rs545378787	snp	A/G			intron-variant	FEM1B	GRCh38.p7	15:68287187	TAAGCCACCGCACCC[A/G]GCCTGATTCATTCTT	10116
rs545408128	snp	C/T			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68291946	TCTTGATGGACTCTG[C/T]CTTTAGGCTTGAATT	10116
rs545685577	snp	A/T	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68288715	CTAATTATTTCCTGC[A/T]GTTAGTATTTTTTTC	10116
rs545780308	snp	A/G	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68285675	GGATATCTTTTGTGA[A/G]GTATACTTGTTCAGT	10116
rs545856799	snp	C/T	1.65031e-05	0.00287251	missense	FEM1B	GRCh38.p7	15:68290569	ATGAAACTGTGAAGG[C/T]CCCAGACATAGAATG	10116
rs545895527	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68291711	TCTGCACATGCCAAA[A/C]TGCTGTAGATAGTTT	10116
rs546071077	snp	C/G/T	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68284010	TCTGCCTCAGCCTCC[C/G/T]GAGTAGCTGGGATTA	10116
rs546082746	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68294410	GAACTTAGGTATGAT[A/C]ACATTGTTTGAAGTA	10116
rs546455893	snp	C/G	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68283775	TAATCAGTTTGGAAA[C/G]GTTCTTTAAATTGAA	10116
rs546542067	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	FEM1B	GRCh38.p7	15:68295992	TAGTAAAGAAAAATT[C/T]AAATATATATTTTAA	10116
rs546745167	snp	C/T	0.00358779	0.0422022	intron-variant	FEM1B	GRCh38.p7	15:68288995	TGTAATAATATAATA[C/T]GTGCTGTGTTCATCT	10116
rs546773112	snp	C/T			intron-variant	FEM1B	GRCh38.p7	15:68283031	GTAATTGGAACTTTT[C/T]TGAGGCTCCTGTCAA	10116
rs547055579	snp	A/G	0.029116	0.117091	intron-variant	FEM1B	GRCh38.p7	15:68285280	ATTAATTAATATTTT[A/G]GTTGTTTCCAGTGTT	10116
rs547085045	snp	A/G	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68281332	GTTCACTAACCTGCT[A/G]TTTACTTAATAAATA	10116
rs547119848	snp	C/T	0.00636936	0.0560724	intron-variant	FEM1B	GRCh38.p7	15:68281774	AGGTGCCCACAACCA[C/T]GCCTGGCTATTTTTT	10116
rs547347539	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68294586	TATTTAAGCAGAAGC[A/G]TTTCTTTTTTTTTTT	10116
rs547381025	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB	FEM1B	GRCh38.p7	15:68277536	CCATCAGCTTAGCGC[C/T]CTCACTCCGCCCCCA	10116
rs547434597	snp	A/G	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68285838	GCACCTGGCCACTTA[A/G]TCGCTTTGTTTATAA	10116
rs547815009	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68293836	AAAATAGGTAAGAAA[A/G]TGATAGTTCTATATC	10116
rs548065777	snp	C/G	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278212	CTGCGCGGGCTGGGT[C/G]GCGGACGTGCCCTTC	10116
rs548310875	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	FEM1B	GRCh38.p7	15:68277680	CCTTTCTCTACCGGG[C/T]CCGCGTGTGCCCGCC	10116
rs548348660	snp	C/G	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68285099	TTGCCTGTACTTGAA[C/G]TTCCTATAAGCAGAA	10116
rs548363346	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	FEM1B	GRCh38.p7	15:68276808	CATCTATCATTCTTA[C/T]TGTGGCCCACTCTGC	10116
rs548474903	snp	A/C	0.000798403	0.0199641	intron-variant, utr-variant-5-prime	FEM1B	GRCh38.p7	15:68278799	TGTACCACCTCCTGC[A/C]CCACTAATGCCCACT	10116
rs548679172	in-del	-/TTGA			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68291932	ACTTTTCAGAGAATC[-/TTGA]TTGATGGACTCTGCC	10116
rs548679316	in-del	-/TA			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68295232	GTGTATAGGGGTAAG[-/TA]TTGCTAAATTATTTA	10116
rs548874630	snp	A/T			intron-variant	FEM1B	GRCh38.p7	15:68287782	GAATCCTGTGTCCTC[A/T]CATGGTGGAAGGTGA	10116
rs549049151	in-del	-/TTAGA	0.00279162	0.0372561	intron-variant	FEM1B	GRCh38.p7	15:68286626	TATTTTCCCATTTAT[-/TTAGA]TTAGATTTACTTATC	10116
rs549232714	snp	A/G	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68286698	TTTTTCATTAGATTT[A/G]TTACTATTTATTGGT	10116
rs549350934	snp	G/T	0.00159617	0.0282053	intron-variant	FEM1B	GRCh38.p7	15:68286601	GAGTCTTCTGGATCA[G/T]GAACATGGAATATTT	10116
rs549535889	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	FEM1B	GRCh38.p7	15:68295951	AAGTTGTCAAAGTTA[C/T]ATATGTGCATGGGAA	10116
rs549870375	snp	C/T			intron-variant	FEM1B	GRCh38.p7	15:68281678	GCTGGAGTGCAGTGG[C/T]GCGATCTCGGCTCAC	10116
rs550020994	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68294654	TTGATTAGTTTGCTG[G/T]TTTAGAAACAGCCAG	10116
rs550377342	snp	G/T			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68295336	GCCAAATGATGAAAT[G/T]AACAAGATTTTGTAT	10116
rs550380569	snp	C/T	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68289250	GAGGAACATGCTGTT[C/T]TCCTAGTAACCAGTG	10116
rs550505779	snp	C/G	0.00119737	0.0244387	intron-variant	FEM1B	GRCh38.p7	15:68282533	ATAGATGAGCTCAGC[C/G]TTGTGATCAGAAATG	10116
rs550507679	snp	G/T	1.64838e-05	0.00287083	missense	FEM1B	GRCh38.p7	15:68290682	ATGGACAATTATGAA[G/T]GTAATCTCTATACCT	10116
rs550640211	snp	A/G			intron-variant	FEM1B	GRCh38.p7	15:68288228	CTTAATGCTATTCAC[A/G]TTTGGCAACACCTGA	10116
rs550840467	snp	C/T	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68280558	TCACAGAGGAGGTGA[C/T]GTTCGAGCTGTGTTT	10116
rs550967721	in-del	-/AAAT	0.00557542	0.0525036	intron-variant	FEM1B	GRCh38.p7	15:68286805	AAAAACATAACAAAA[-/AAAT]AACAAAAGTGAATTT	10116
rs551302256	snp	C/G	0.000798403	0.0199641	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68292011	TGCAGCAGTCTATTT[C/G]ATTCAGCTCATAGAC	10116
rs551333878	snp	A/T			intron-variant	FEM1B	GRCh38.p7	15:68289153	TTCTTCTTAAAGCAG[A/T]GTCTAACACAGCTTT	10116
rs551351769	snp	A/G			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68293591	TGAACTATGCTAATG[A/G]TAATTAGATTTTTTG	10116
rs551353780	snp	C/T			downstream-variant-500B	FEM1B	GRCh38.p7	15:68296168	CTACCTTTGCAACGC[C/T]ATTCTGTATCTTATC	10116
rs551621597	snp	C/T	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68286770	TAAATGTTTATTGAA[C/T]TTTACATAATCATGA	10116
rs551702742	snp	A/G	0.00199481	0.0315187	intron-variant	FEM1B	GRCh38.p7	15:68289123	GCTTAGGGGAAACTT[A/G]CCTGCTTTATTTTTT	10116
rs551926593	snp	C/T	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68287402	GGACATTTCCAGTAC[C/T]TTCAAGTCTCTTCCC	10116
rs552004396	snp	A/G	0.00119737	0.0244387	intron-variant, utr-variant-5-prime	FEM1B	GRCh38.p7	15:68279065	ACATTGAAGAACTCC[A/G]AAAGAGTTATTTGGG	10116
rs552016479	snp	A/G	0.000798403	0.0199641	intron-variant	FEM1B	GRCh38.p7	15:68280409	ATGTCAGTCTGGGTG[A/G]GGGGAGAGAAATTAA	10116
rs552159162	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	FEM1B	GRCh38.p7	15:68277593	GTTTAGGGGCCAGGA[A/G]GAGGTTCCAGGAGTC	10116
rs552265211	snp	A/G	0.000399281	0.0141238	missense	FEM1B	GRCh38.p7	15:68289857	GCATATAAGGGACAC[A/G]CTGATGTGGTCAGAT	10116
rs552299455	snp	C/T	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68283819	CAATGATGTGTACTA[C/T]GTTTCCTTACGTTTG	10116
rs552350033	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68292156	TACTTTTCCAGAAGG[C/T]ATTATTTATGCCTCC	10116
rs552456623	snp	A/C	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278172	GCGCCTGGGACCTGG[A/C]GGGCGGCCCTGACCG	10116
rs552525266	snp	C/T			intron-variant	FEM1B	GRCh38.p7	15:68285123	AGCAGAATTATGTAG[C/T]ATGTACTCTTTTTGT	10116
rs552874326	snp	A/T	0.00159617	0.0282053	intron-variant	FEM1B	GRCh38.p7	15:68283826	GTGTACTATGTTTCC[A/T]TACGTTTGATGCATT	10116
rs552948814	snp	A/G	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68288694	CTGCTTGGTTTTCCA[A/G]AAGTGCTAATTATTT	10116
rs553383332	snp	A/G	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68280896	TTATTAAATGCTTGT[A/G]ATGGGCCTAGCCTGT	10116
rs554085582	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68291595	TACAAAAGTATTTCT[C/G]TTAAGCCTATGTCAG	10116
rs554122008	snp	A/G	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68283941	CCGAGGCTAAAGTGC[A/G]ATGGCGTGATCTTGG	10116
rs554334821	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	FEM1B	GRCh38.p7	15:68277046	TCTTGTCTATCATTT[A/G]TTGACTTATTTGTTC	10116
rs554486995	snp	C/T	0.000798403	0.0199641	intron-variant	FEM1B	GRCh38.p7	15:68284654	TCACTCTAAAAGTTT[C/T]CCTTGTGCCCCTTCT	10116
rs554655496	snp	C/G			intron-variant	FEM1B	GRCh38.p7	15:68282275	TTGTTCTTTTAAAGT[C/G]AGTGCTAGTACTAAT	10116
rs554876974	in-del	-/T	0.00119737	0.0244387	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68292409	CAGAGGTCTTTATGG[-/T]TTTTTTTGTTTTGTT	10116
rs555227182	in-del	-/TTCTT			intron-variant	FEM1B	GRCh38.p7	15:68289014	CTGTGTTCATCTGAC[-/TTCTT]TTCTCAGCATCAGGT	10116
rs555257375	snp	G/T	9.88794e-05	0.00703064	missense	FEM1B	GRCh38.p7	15:68290347	ATATGGAAGGCCTTA[G/T]AGTTCGGGAACGGAT	10116
rs555314964	in-del	-/A	0.00795532	0.062565	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68293812	ACTTAATTTTTTTTT[-/A]AAAAAAGGAAAATAG	10116
rs555481504	snp	C/T	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68285475	CAAATTACATTCCTA[C/T]TTGCAGTTTCCACCA	10116
rs555522629	snp	A/G	3.31609e-05	0.00407177	missense, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278530	GCTATCTGCTTGGCT[A/G]TGTCAGCCAGCAGGG	10116
rs555653055	snp	A/G	0.000798403	0.0199641	intron-variant	FEM1B	GRCh38.p7	15:68287015	GCCTCAGCCTCCTGC[A/G]TAGCTGGGATTACAA	10116
rs556273091	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68292608	CCTTAGCTACTCATA[A/G]TGCATGGTACTGTAA	10116
rs556483121	in-del	-/T	0.0209421	0.100162	intron-variant	FEM1B	GRCh38.p7	15:68287831	CGTTGCTAACGTCTC[-/T]TTTTTTTTTTTTTTT	10116
rs556500605	snp	A/C	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68284744	CTATGTCCCACCCAA[A/C]TCTTATCTTGAATTC	10116
rs556528623	snp	C/T	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68286273	CCGTGCCAGCACTTA[C/T]TTTAATTACTGTAGT	10116
rs556593620	snp	C/T	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68288109	TACTGAGATGATAGG[C/T]GTGAGCCACCATGCC	10116
rs556776903	snp	A/G	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68285384	TATATATCAAGGAGT[A/G]GAATTGCTGGGTCAT	10116
rs556796726	snp	A/G	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68281877	CCTCGGCCTCCCTAA[A/G]TGCTGGGATTACAGG	10116
rs556864855	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278400	GCGACCAAACGGGTG[C/T]TGGAGTTGGCGGCGG	10116
rs557075280	snp	G/T			intron-variant	FEM1B	GRCh38.p7	15:68285905	ATCCAATAAATACTT[G/T]CTTTTTCTTTAACGG	10116
rs557098299	snp	C/T	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68279146	GCTGCTGGGCTTTAA[C/T]GTCAAAATAAGCACC	10116
rs557366042	snp	A/G	0.00119737	0.0244387	intron-variant	FEM1B	GRCh38.p7	15:68288410	ATATTCCTTTGATCA[A/G]CCTTTCTTCTTAACA	10116
rs557382398	snp	C/T	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68279658	GTGATTAGAAACTGC[C/T]TGGCTAAAACTCGAC	10116
rs557412210	snp	C/T	0.00279162	0.0372561	intron-variant	FEM1B	GRCh38.p7	15:68286877	TCACTGATGTAGTGT[C/T]TTATTTTCTTGATTC	10116
rs557815603	snp	G/T	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68281448	TTGCTGTGTGTTTTG[G/T]GTGTGTGCGTGAGAA	10116
rs557891347	snp	G/T	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68285608	GTTTTAATTTGCATT[G/T]CCCTGTTAACTAATT	10116
rs557956809	snp	A/T	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68287908	GCACGATGTCAGCTC[A/T]CGGCAACCTCTGCCT	10116
rs557991532	snp	G/T	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68281017	GTTCCTGGTACTCTC[G/T]GTGCATTCACACCTT	10116
rs558038941	snp	A/G			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68293499	TTGAGAAGGGAAGAC[A/G]ATGCTGAAGAAAGTA	10116
rs558046515	snp	G/T	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68279562	GGTTGACTTGTGGTA[G/T]TACATAAGCTATTTT	10116
rs558183988	snp	G/T	0.000798403	0.0199641	intron-variant	FEM1B	GRCh38.p7	15:68286236	TTTTTTTTTTTGGTC[G/T]GTTGATAATATTATT	10116
rs558330915	snp	A/G	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68282895	TATTTTGATTTAGAT[A/G]TAGAAATTCTAAATT	10116
rs558416602	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	FEM1B	GRCh38.p7	15:68276477	CATTTGTTCTTTCTC[G/T]ATGGTAAATTTTGTC	10116
rs558607860	snp	C/T	0.000164919	0.00907921	synonymous-codon	FEM1B	GRCh38.p7	15:68290231	TGGTGATAACATTCT[C/T]GAAAAAGAGGTTCTT	10116
rs558702389	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	FEM1B	GRCh38.p7	15:68276929	CGTCTGTTCTTGTCA[C/T]TTGTCATAGAGGTCT	10116
rs558973244	snp	A/C	0.00119737	0.0244387	intron-variant	FEM1B	GRCh38.p7	15:68281622	ATTTGAGTTCTTGTT[A/C]ACTTTTTTTTTTTGA	10116
rs559402686	snp	A/G			intron-variant	FEM1B	GRCh38.p7	15:68281221	CAGCACTTGAGACAC[A/G]TGGCCATATAGGGAT	10116
rs559646811	snp	C/T	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68280278	AATGTTCTGTACTGG[C/T]CAGAGAAATTAATGA	10116
rs559653732	snp	C/T	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68287637	TGTTCTGTGGTGTTA[C/T]AACAAAATACCTGAC	10116
rs559984814	snp	A/G	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68287288	CTGATCTTTTCTGAG[A/G]TATGTCTTACATACA	10116
rs559990345	snp	A/G			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68294812	TCTCACTGACTATAT[A/G]ACATTAAAAAGGGGT	10116
rs560100347	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68292088	GTGTAGTTATACATT[C/G]TATTTTTGTCCCCTT	10116
rs560395551	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68293220	CAGATCAGACCCTTT[A/G]TTTTTCAAACTACAA	10116
rs560416090	snp	A/T			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68293744	ACATGCCTGTTTTTT[A/T]AAAATGTTTTTGGTA	10116
rs560595988	snp	A/G	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68282288	GTCAGTGCTAGTACT[A/G]ATACTTCTGATAAAT	10116
rs560604592	snp	A/G	0.000798403	0.0199641	intron-variant	FEM1B	GRCh38.p7	15:68282323	AGGCGGAGGAAAGGC[A/G]TGAGGGGCATGCCAG	10116
rs560690495	snp	A/G	0.00279162	0.0372561	upstream-variant-2KB	FEM1B	GRCh38.p7	15:68275806	CAGAAAGTTGGTTCG[A/G]AATAGAATGTAGAAT	10116
rs560751146	snp	C/T	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68283170	TAATTTTTACTCTTA[C/T]ATCATAGATTCTGAG	10116
rs560906565	snp	G/T	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68284353	TTGGCACTGTATTTG[G/T]TATAAATTACCAAAG	10116
rs561485550	snp	A/C	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68281710	GCAAGCTCTGCCTTC[A/C]GGGTTCATGCCATTC	10116
rs561528969	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68293630	GTATAGTGGTAAATT[A/G]TGTAGTATCTTGCTG	10116
rs561763757	snp	A/T	0.00279162	0.0372561	intron-variant	FEM1B	GRCh38.p7	15:68284114	GGTCTTGAACTACCC[A/T]CCTCAGGTGATCCAC	10116
rs561794745	snp	C/G/T	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68285792	TCTTCTTAGCCCCCC[C/G/T]GCAGTGCTGGGATTA	10116
rs561800763	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	FEM1B	GRCh38.p7	15:68277522	GTGGTCTCCTTAGCC[C/T]ATCAGCTTAGCGCCC	10116
rs561812120	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68294475	CAACTCTGTTTGACA[A/G]ATGTTTTGAAAATTA	10116
rs561845635	in-del	-/ATGTT	0.00119737	0.0244387	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68291516	AGGAACAGATATAAA[-/ATGTT]TTGTTTATGTAACAA	10116
rs561877693	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	FEM1B	GRCh38.p7	15:68278800	GTACCACCTCCTGCC[C/G]CACTAATGCCCACTT	10116
rs561879584	snp	C/T	0.00318978	0.0398085	intron-variant	FEM1B	GRCh38.p7	15:68286407	TTAGAGAGAGGTTCT[C/T]GCACTGTTGCTCAGG	10116
rs561889622	snp	A/C	0.000798403	0.0199641	utr-variant-5-prime, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68277886	CGCCTGGCACTTCTG[A/C]GCTCGGCGGACGAGA	10116
rs561987461	in-del	-/AT	0.00874735	0.0655527	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68294209	ACTGACACTGAAAAC[-/AT]AGCTTTTTCAGTCCA	10116
rs562220205	snp	A/G			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68293847	GAAAATGATAGTTCT[A/G]TATCTCAGCCCTCTG	10116
rs562364123	snp	A/G			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68291454	TGTTTTGGTGTAACT[A/G]TAAGGTATTTGCATA	10116
rs562550117	snp	C/G	1.65034e-05	0.00287253	missense	FEM1B	GRCh38.p7	15:68290574	ACTGTGAAGGCCCCA[C/G]ACATAGAATGTGTTT	10116
rs562759354	in-del	-/TT	0.0023933	0.0345097	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68291423	TGATTTCAGACAGAC[-/TT]TAACAAAACCACATT	10116
rs562766248	snp	C/T	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68285738	AGGATCTTGCTGTGT[C/T]GCGCAGGCTGGTCTT	10116
rs562834285	snp	C/T	0.00127781	0.0252442	synonymous-codon, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278651	TCAGCAGACTGGCAC[C/T]GTCCGCTTCGACGGG	10116
rs562834979	snp	A/T	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68283421	GTAATCCCAGCACTT[A/T]GGGAGGCCTAGGTGG	10116
rs563033867	snp	A/G	0.0023933	0.0345097	intron-variant	FEM1B	GRCh38.p7	15:68284031	GCTGGGATTACAGAC[A/G]TGCGCCACCACACCT	10116
rs563037645	in-del	-/TG			intron-variant	FEM1B	GRCh38.p7	15:68283052	CTCCTGTCAAATGAC[-/TG]TAGCTCAAGGGAAAA	10116
rs563280936	snp	A/T	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68281073	CCAGTCATTTTAGGA[A/T]TTTAGAACCAAAAAA	10116
rs563419894	snp	C/T			intron-variant	FEM1B	GRCh38.p7	15:68287133	TGACCTCCGGTGATC[C/T]GCCTGCTTTGGCCTC	10116
rs563632467	snp	G/T	0.000399281	0.0141238	downstream-variant-500B	FEM1B	GRCh38.p7	15:68295873	AAAAACTACTTTGAG[G/T]TTTGTGTCTTTATTA	10116
rs563670536	snp	A/G	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68286655	TCTCAGGAGTGTTTT[A/G]TAGTTTTCAGTGTAG	10116
rs563709753	snp	A/T	0.00279162	0.0372561	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68294616	TTGGAATGGGGTGGG[A/T]TGAGGAGTGAGTTGC	10116
rs563748477	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68295655	CCATTTATGTGACTT[C/T]AATAAACATAGTAAA	10116
rs564060731	snp	C/T	0.00159617	0.0282053	intron-variant	FEM1B	GRCh38.p7	15:68287125	CGAACTCCTGACCTC[C/T]GGTGATCCGCCTGCT	10116
rs564151117	snp	C/G	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68280011	TCTGAACCTCCAGTA[C/G]CGTTCCACCTGTATA	10116
rs564161785	snp	C/T	0.00517822	0.0506191	utr-variant-5-prime, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278014	GCGCCCATCTTTCGC[C/T]ATCCGGGGTGCGCGA	10116
rs564202155	snp	A/G	1.65444e-05	0.00287609	missense, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278581	TCATCATCGCAGCCC[A/G]CAATGGACACGCAAA	10116
rs564207080	snp	C/T	0.000798403	0.0199641	intron-variant	FEM1B	GRCh38.p7	15:68286568	ATTTTGAGGGAGAAT[C/T]GACATCTTAACATTA	10116
rs564242738	snp	C/T	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68279305	TGGGAGATGATGCCA[C/T]TCTTAAATTACATCT	10116
rs564506822	snp	A/G			upstream-variant-2KB	FEM1B	GRCh38.p7	15:68277565	CACTCCCTGGCTGGA[A/G]ACCCTCAGGGCCGTT	10116
rs565484278	snp	C/T	0.00159617	0.0282053	intron-variant	FEM1B	GRCh38.p7	15:68288227	TCTTAATGCTATTCA[C/T]GTTTGGCAACACCTG	10116
rs565648577	in-del	-/GCGGCG	0.00478085	0.0486577	utr-variant-5-prime, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278284	CACTGCTGCCTGGGC[-/GCGGCG]GCGGCGGCGGCGACG	10116
rs565909385	snp	C/G	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68286019	TTTTATTTTGAGAAG[C/G]TTTTCACACTATAGG	10116
rs566116870	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	FEM1B	GRCh38.p7	15:68295975	ATGGGAAAAAATTCA[C/T]GTAGTAAAGAAAAAT	10116
rs566153609	snp	C/T	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68286718	TATTTATTGGTATTT[C/T]CTGATGCTGTTGCAA	10116
rs566466114	snp	A/C	0.000798403	0.0199641	upstream-variant-2KB	FEM1B	GRCh38.p7	15:68277552	CTCACTCCGCCCCCA[A/C]TCCCTGGCTGGAGAC	10116
rs566596774	snp	A/G			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68292347	TAATTGTGTCTGAGA[A/G]CTGCAAATTTTTCAA	10116
rs566968778	snp	A/G	0.0023933	0.0345097	intron-variant	FEM1B	GRCh38.p7	15:68281779	CCCACAACCATGCCT[A/G]GCTATTTTTTGTATT	10116
rs567126778	snp	A/G	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68281898	GGATTACAGGCTTGA[A/G]CCACTGTGCGCGGCC	10116
rs568011586	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68292238	AATTTTTTCACTTTC[G/T]TAGTCTGTGACAAGA	10116
rs568149640	snp	C/T	0.000798403	0.0199641	intron-variant	FEM1B	GRCh38.p7	15:68285150	TTGTTTGGCTTTTTT[C/T]GCTTAACACAGTGTC	10116
rs568151539	snp	C/G	0.000798403	0.0199641	upstream-variant-2KB	FEM1B	GRCh38.p7	15:68277682	TTTCTCTACCGGGCC[C/G]GCGTGTGCCCGCCGG	10116
rs568455704	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	FEM1B	GRCh38.p7	15:68276836	TGCTGCAGCCACACT[A/G]ACCTTTCTGTTTCCG	10116
rs568646077	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68291467	CTATAAGGTATTTGC[A/C]TATTGGTTACCTATT	10116
rs568802734	snp	A/G	0.00159617	0.0282053	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68293228	ACCCTTTATTTTTCA[A/G]ACTACAAGGCCTGCT	10116
rs568876101	snp	C/T	1.66366e-05	0.0028841	missense	FEM1B	GRCh38.p7	15:68291174	GCTGCCCGAGCAGTT[C/T]GGGCTAATGACATTA	10116
rs568964152	snp	C/T	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68284505	ATTTTTGTTTTTAAT[C/T]ATATCTGTTTTTTTA	10116
rs568967252	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68292171	CATTATTTATGCCTC[A/C]CTAATAAGGTATTTT	10116
rs569128260	snp	C/G	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68281847	TCTCGATCTCCTGAC[C/G]TCGTGATCCGCATGC	10116
rs569329301	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	FEM1B	GRCh38.p7	15:68275923	GTAATCAAAGTGTGT[A/T]GGCAGAGGAGAGGGA	10116
rs569674067	in-del	-/A	0.00517822	0.0506191	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68292062	GTTTTCTTATGAAAC[-/A]AATTGTCACAGTGTA	10116
rs569881342	snp	A/G/T	0.000399281	0.0141238	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68293916	CATTTGATGTTTACT[A/G/T]TTGGTATACTTATGC	10116
rs569891439	in-del	-/TAGGCGTGTGC	0.00199481	0.0315187	intron-variant	FEM1B	GRCh38.p7	15:68287970	TCCTATCTGGGATTA[-/TAGGCGTGTGC]CACCATGCCCGGCTA	10116
rs569943657	snp	C/G	0.000399281	0.0141238	downstream-variant-500B	FEM1B	GRCh38.p7	15:68296280	TGATGGATTGAAAAT[C/G]TATTTAACTAGATTT	10116
rs569958085	in-del	-/CTGA	0.000798403	0.0199641	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68295492	GTTGGGGAGTAAAAT[-/CTGA]CTGGCCTAATCGATG	10116
rs570004170	in-del	-/GCTTTTCCTTACTG			intron-variant	FEM1B	GRCh38.p7	15:68279916	ACCTGATTCATGTTT[-/GCTTTTCCTTACTG]GCTTTCGTGTCTTCT	10116
rs570006003	snp	C/T	0.00159617	0.0282053	intron-variant	FEM1B	GRCh38.p7	15:68285902	GAAATCCAATAAATA[C/T]TTTCTTTTTCTTTAA	10116
rs570331567	snp	A/C	0.0103295	0.0711199	intron-variant	FEM1B	GRCh38.p7	15:68281231	GACACATGGCCATAT[A/C]GGGATTAACAGCTGT	10116
rs570358613	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	FEM1B	GRCh38.p7	15:68278869	CCCGTCCTCATCAGC[C/T]CCTACCCCTCATTCC	10116
rs570361646	snp	A/G	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68285841	CCTGGCCACTTAATC[A/G]CTTTGTTTATAATGT	10116
rs570453155	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	FEM1B	GRCh38.p7	15:68278829	TTCATCTTCCAGGGC[C/T]AATAATCCATCCCAT	10116
rs570469364	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278319	CCTGTTGAATGGGCT[A/G]TGAGGGCCCAGGTTT	10116
rs570585723	in-del	-/TGTT	0.00557542	0.0525036	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68291562	ATTTCAAGTTGATAA[-/TGTT]TGTTTTAAACAGCTG	10116
rs571003036	snp	G/T	0.000798403	0.0199641	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68292508	TTCAAGTGAAAGTTA[G/T]ATGCTTATTTCTATT	10116
rs571115429	snp	A/G	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68288519	GTAAGAAATTTAGAA[A/G]TTAAGGTTGGGGAAA	10116
rs571152744	in-del	-/TT			intron-variant	FEM1B	GRCh38.p7	15:68283886	TAATCTCACGTAAAC[-/TT]TTTTTTTTTTTTTTT	10116
rs571720506	snp	G/T	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68287562	TAGAAGTGATAAAGG[G/T]TATTGTTTTTTGTGG	10116
rs571754718	snp	A/G	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68280523	AGTGCTGTTTTATCC[A/G]GGGGGAATCTAGAAA	10116
rs571784769	snp	A/G	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68279578	TACATAAGCTATTTT[A/G]GCATTTTTTTTTTCT	10116
rs572127256	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68295487	ACACAGTTGGGGAGT[A/G]AAATCTGACTGGCCT	10116
rs572183257	in-del	-/CCT	0.00119737	0.0244387	downstream-variant-500B	FEM1B	GRCh38.p7	15:68296032	TTTCATCTCTCCCCG[-/CCT]CCTATTTGGACTCTG	10116
rs572195134	snp	G/T	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68287066	TGGCTAATTTTTGTA[G/T]TATTGGTAGAGACGG	10116
rs572195570	snp	A/C	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68285530	TCTTGCTCAACACTT[A/C]TTATTGCCCTGTCAG	10116
rs572398922	snp	A/G	0.00199481	0.0315187	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68294148	AGGAATGGGCGGCAA[A/G]CCCATCCCCTCGATT	10116
rs572548429	snp	A/G	0.00279162	0.0372561	intron-variant	FEM1B	GRCh38.p7	15:68281641	TTTTTTTTTTGAGAC[A/G]GAGTCTCGCTCTGTC	10116
rs572710154	snp	C/T	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68288710	AAGTGCTAATTATTT[C/T]CTGCTGTTAGTATTT	10116
rs572860005	snp	A/G			intron-variant	FEM1B	GRCh38.p7	15:68281011	ATTGAAGTTCCTGGT[A/G]CTCTCTGTGCATTCA	10116
rs573248922	snp	A/G	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68280910	TGATGGGCCTAGCCT[A/G]TGTCATGTTCTGGAG	10116
rs573339987	snp	C/G	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68288110	ACTGAGATGATAGGC[C/G]TGAGCCACCATGCCA	10116
rs573941866	snp	C/T	0.000798403	0.0199641	intron-variant	FEM1B	GRCh38.p7	15:68279199	ATCATGAGGGATTGT[C/T]ACGCAGCCAGACATC	10116
rs574450615	snp	C/T	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68283862	GTATTCCAAGTACTT[C/T]TGTATTTTTAATCTC	10116
rs574458753	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	FEM1B	GRCh38.p7	15:68276600	CCATCCTAATCCAAG[A/G]CCTGTCCCCCTATCT	10116
rs574487193	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	FEM1B	GRCh38.p7	15:68277207	TCAGGATGAGATTCC[C/T]GCTCTGTCTGAACGC	10116
rs574613745	in-del	-/T			intron-variant	FEM1B	GRCh38.p7	15:68280379	ATGAATAACATACTC[-/T]TTTTGTCTTGGAGGA	10116
rs574903632	snp	C/G	0.00755907	0.0610114	intron-variant	FEM1B	GRCh38.p7	15:68284760	TCTTATCTTGAATTC[C/G]CACGTGTTGTGGGAG	10116
rs575025283	snp	C/T	1.64836e-05	0.0028708	synonymous-codon	FEM1B	GRCh38.p7	15:68290420	CAGAGGAGCTGTTTA[C/T]GCGGATAATATGGAA	10116
rs575172167	snp	A/G	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68283065	ACTGTAGCTCAAGGG[A/G]AAAAAATGGAAATTA	10116
rs575201838	snp	C/T	0.000798403	0.0199641	intron-variant	FEM1B	GRCh38.p7	15:68282923	ATTTACCAAGGCTAA[C/T]GTTTCTGAAGGACCA	10116
rs575277852	snp	A/G	6.59663e-05	0.00574272	synonymous-codon	FEM1B	GRCh38.p7	15:68290240	CATTCTCGAAAAAGA[A/G]GTTCTTCCACCAATC	10116
rs575290524	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	FEM1B	GRCh38.p7	15:68276502	TTTGTCCTTTGGGGA[A/G]GGGAGGAAGAGGGAG	10116
rs575667771	snp	C/G	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68289361	GTTCGTGATTTTTCA[C/G]GTTTGTTTTTTAGGG	10116
rs575989227	snp	A/G	0.000399281	0.0141238	missense, utr-variant-5-prime	FEM1B	GRCh38.p7	15:68289641	ACTGCTCTTTGGTGT[A/G]CAGCTGGAGCAGGAC	10116
rs576104676	snp	A/G	0.00119737	0.0244387	intron-variant	FEM1B	GRCh38.p7	15:68284076	TTTTAGTAGAGATGG[A/G]GTTTTTCCGTGTTGG	10116
rs576106272	snp	C/T	0.00119737	0.0244387	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68292689	TGTAGCAGCATCAGA[C/T]ATAAACTTAAAAAAA	10116
rs576195127	snp	C/G	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68284759	ATCTTATCTTGAATT[C/G]CCACGTGTTGTGGGA	10116
rs576355982	snp	A/G			synonymous-codon, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278450	CTATGTATACAAGGC[A/G]GCCAGCGAGGGCAAG	10116
rs576877081	snp	A/C	0.000798403	0.0199641	utr-variant-5-prime, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68277803	CCCAAGTTCCGGCGC[A/C]GCTCTTGCGGGAGCG	10116
rs577141810	in-del	-/AG	0.0023933	0.0345097	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68293538	GATTGAAATGCTGAC[-/AG]GGTGGAGAACGAATT	10116
rs577180581	snp	G/T			intron-variant	FEM1B	GRCh38.p7	15:68289350	GCTAGTAGAAAGTTC[G/T]TGATTTTTCAGGTTT	10116
rs577191180	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68294315	CCCAAAGCAGACCAT[C/T]TGTAAGCTTTGGTCT	10116
rs577325208	snp	A/T	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68283203	GTTTGAGATCAGAAA[A/T]ATATTTTAATCACTT	10116
rs577325645	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68291604	ATTTCTGTTAAGCCT[A/G]TGTCAGCATGTTATC	10116
rs577596852	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	FEM1B	GRCh38.p7	15:68277291	CCCCTTCGCTCCCAT[C/G]TTTCTCTCACACTTA	10116
rs577764882	snp	A/T	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68281068	TTATCCCAGTCATTT[A/T]AGGATTTTAGAACCA	10116
rs577861201	snp	C/T	0.000798403	0.0199641	intron-variant	FEM1B	GRCh38.p7	15:68281456	TGTTTTGTGTGTGTG[C/T]GTGAGAAAGACATAC	10116
rs577936528	snp	A/T	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68285662	TTATGGGCCATTTGG[A/T]TATCTTTTGTGAAGT	10116
rs577993109	snp	C/T	0.000399281	0.0141238	intron-variant	FEM1B	GRCh38.p7	15:68286239	TTTTTTTTGGTCTGT[C/T]GATAATATTATTCTG	10116
rs578020857	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	FEM1B	GRCh38.p7	15:68279080	GAAAGAGTTATTTGG[A/G]CATCCATTTTTACTC	10116
rs578039059	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68295100	TTGATAGTGGAGATA[C/T]ATTAATTTTTAAAAC	10116
rs745343555	snp	A/G			intron-variant	FEM1B	GRCh38.p7	15:68279522	ACAGATTACAACTGT[A/G]TAACGATTTTGCTAC	10116
rs745422772	snp	C/T			intron-variant, utr-variant-5-prime	FEM1B	GRCh38.p7	15:68279053	GGTCAGCGGTTAACA[C/T]TGAAGAACTCCGAAA	10116
rs745493809	snp	G/T	1.67206e-05	0.00289137	intron-variant, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278700	GCCTCTCTCCGACGC[G/T]CGCGGACTCGTTAAT	10116
rs745539219	snp	C/T	9.89642e-05	0.00703365	synonymous-codon, utr-variant-5-prime	FEM1B	GRCh38.p7	15:68289697	CAGCCATGGAGCCAA[C/T]GTGAACCATACCACA	10116
rs745611308	snp	C/T			intron-variant	FEM1B	GRCh38.p7	15:68287049	TGTGCCACCACCACT[C/T]CTGGCTAATTTTTGT	10116
rs745751102	snp	C/G			intron-variant	FEM1B	GRCh38.p7	15:68287349	TGGTGAGTTTTTTCC[C/G]TAAATATCCATGTGG	10116
rs745809434	snp	A/G			upstream-variant-2KB	FEM1B	GRCh38.p7	15:68276189	AGCTATTTCAGAGAC[A/G]CTACCAGTAGAATCT	10116
rs745838677	snp	C/T	1.6476e-05	0.00287014	missense	FEM1B	GRCh38.p7	15:68290733	TCTACCAAAACACAG[C/T]GCAGCGAAGAAGATC	10116
rs745899938	snp	A/G			intron-variant	FEM1B	GRCh38.p7	15:68282198	ACCTGTCCTTGAAGG[A/G]GTTTGCTGATGTGGA	10116
rs745995263	snp	C/T	1.64732e-05	0.0028699	synonymous-codon	FEM1B	GRCh38.p7	15:68290969	AAACAGTGCCCTTCA[C/T]ATTATCGTTCAGTAC	10116
rs746085028	snp	C/G	1.67987e-05	0.00289811	missense, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278475	GGCAAGGTGCTGACT[C/G]TGGCCGCCTTGCTTC	10116
rs746099220	snp	A/C			intron-variant	FEM1B	GRCh38.p7	15:68283993	CAGGTTCAAGCAATT[A/C]TTCTGCCTCAGCCTC	10116
rs746155763	snp	A/G			intron-variant	FEM1B	GRCh38.p7	15:68281649	TTGAGACGGAGTCTC[A/G]CTCTGTCGCCGGGGC	10116
rs746211167	snp	A/C			intron-variant	FEM1B	GRCh38.p7	15:68284144	CCCACCTTGGCCTCC[A/C]AAAGTGTTGGGATTA	10116
rs746375298	snp	C/G	3.2987e-05	0.00406108	synonymous-codon	FEM1B	GRCh38.p7	15:68290123	TGAAGCTTTGGAACT[C/G]TTGGGTGCCTCCTTT	10116
rs746564988	snp	A/C			intron-variant	FEM1B	GRCh38.p7	15:68280739	TGGTGATCCCTGTAT[A/C]AAGTACTAAGAGTAA	10116
rs746655946	snp	A/C	1.65116e-05	0.00287324	missense	FEM1B	GRCh38.p7	15:68289977	ATTGTGAAAGAGCTG[A/C]TAAAATGGCGTGCTG	10116
rs746733838	in-del	-/AAC	5.79022e-05	0.00538031	intron-variant	FEM1B	GRCh38.p7	15:68289581	TGGCCTCTGTTATCT[-/AAC]AACTGCTTATTCTTT	10116
rs746742290	snp	A/C			upstream-variant-2KB	FEM1B	GRCh38.p7	15:68277375	GTGTTGTGGCTCTCA[A/C]GCCCTCCCACATTTC	10116
rs746786246	snp	A/G			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68291263	TGGATATGTAAAGTC[A/G]TTTAATGTGGTGCTA	10116
rs746831997	snp	A/G			intron-variant	FEM1B	GRCh38.p7	15:68288751	GTGGTTGATTGAGGA[A/G]CACACAGACAAGCAG	10116
rs746907604	snp	A/G	1.6473e-05	0.00286988	missense	FEM1B	GRCh38.p7	15:68290986	TTATCGTTCAGTACA[A/G]CAGGCCCATCAGTGA	10116
rs746922168	snp	A/G	1.66418e-05	0.00288455	missense, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278502	CTTCTCAACCGGTCT[A/G]AAAGCGACATCCGCT	10116
rs746966709	snp	A/G	1.64958e-05	0.00287187	synonymous-codon	FEM1B	GRCh38.p7	15:68291107	CAAAAGTACAACTGG[A/G]GTATCTGAAATACTG	10116
rs746968672	snp	A/G			utr-variant-5-prime, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68277952	GCGGAAAGCGCAGGA[A/G]GAGGCAGTGTTAGGC	10116
rs747008030	snp	C/T			intron-variant	FEM1B	GRCh38.p7	15:68285432	AACTAACAGATATTG[C/T]CAAATAGTTTCCCCA	10116
rs747060338	snp	C/T	1.65468e-05	0.00287631	synonymous-codon, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278573	CACGCCCCTCATCAT[C/T]GCAGCCCGCAATGGA	10116
rs747171766	in-del	-/TATAA			intron-variant	FEM1B	GRCh38.p7	15:68284235	AGTTAATATTATAAC[-/TATAA]TATAATAGTATAATA	10116
rs747264002	snp	C/T	1.64942e-05	0.00287173	missense	FEM1B	GRCh38.p7	15:68290134	AACTCTTGGGTGCCT[C/T]CTTTGCAAATGACCG	10116
rs747331493	snp	A/C			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68293799	CAGACCCTTCCCCAA[A/C]TTAATTTTTTTTTAA	10116
rs747427324	snp	A/C	3.29582e-05	0.00405931	missense	FEM1B	GRCh38.p7	15:68290307	CAGGAACTGGAGTCC[A/C]TTCGGCAAGACAGAG	10116
rs747489511	in-del	-/AA			intron-variant	FEM1B	GRCh38.p7	15:68286812	TAACAAAAAAATAAC[-/AA]AAGTGAATTTTAATT	10116
rs747511055	snp	A/T	1.64879e-05	0.00287118	missense	FEM1B	GRCh38.p7	15:68290480	TGCCCTGCACCTCAG[A/T]CAAAAAGGTAACAGG	10116
rs747511058	snp	A/G			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68294781	TGTGTTGATGCACAC[A/G]TGACTATTCTGTTTT	10116
rs747596297	snp	C/G			intron-variant	FEM1B	GRCh38.p7	15:68288831	ATAACGTAACTTAGA[C/G]AAAAATGCACTAATT	10116
rs747664228	snp	A/G	1.64939e-05	0.0028717	missense	FEM1B	GRCh38.p7	15:68290104	GCGACCGAAGAAGTC[A/G]GATTGAAGCTTTGGA	10116
rs747831755	snp	C/G	1.64735e-05	0.00286993	synonymous-codon	FEM1B	GRCh38.p7	15:68291011	CAGTGATTTTTTGAC[C/G]TTGCACTCCATCATC	10116
rs747986377	snp	C/G			utr-variant-5-prime, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68277996	GGCCGGGTCAGGAGA[C/G]ACGCGCCCATCTTTC	10116
rs748025889	snp	A/G	1.65425e-05	0.00287593	missense, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278584	TCATCGCAGCCCGCA[A/G]TGGACACGCAAAGGT	10116
rs748103951	snp	A/T	1.69691e-05	0.00291278	intron-variant, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278680	GGTAGGTACATCCCA[A/T]GCCAGCCTCTCTCCG	10116
rs748174240	in-del	-/CTT	2.01227e-05	0.0031719	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68291290	CTAAAAAGTAAAGGA[-/CTT]CTTTTAATCACAGAC	10116
rs748286036	snp	A/G			intron-variant	FEM1B	GRCh38.p7	15:68286750	TGTTATTTTTTGACA[A/G]TAAATAAATGTTTAT	10116
rs748386645	snp	A/G	3.29598e-05	0.00405941	missense	FEM1B	GRCh38.p7	15:68290325	CGGCAAGACAGAGAT[A/G]CTCTTCATATGGAAG	10116
rs748496828	snp	C/G			intron-variant	FEM1B	GRCh38.p7	15:68281021	CTGGTACTCTCTGTG[C/G]ATTCACACCTTCTGT	10116
rs748584893	snp	A/G			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68294934	AGCTTTGTTCTGGAT[A/G]TCATCTCTTGAAAGT	10116
rs748599497	snp	A/C			upstream-variant-2KB	FEM1B	GRCh38.p7	15:68277735	ACTTAGCGTCCCTCC[A/C]GCTCCCGCCCTCTCC	10116
rs748606352	snp	A/G			intron-variant	FEM1B	GRCh38.p7	15:68281857	CTGACCTCGTGATCC[A/G]CATGCCTCGGCCTCC	10116
rs748722330	snp	G/T			intron-variant	FEM1B	GRCh38.p7	15:68279278	GCTACTAAGATGGCA[G/T]TGGACCTGATGTGGG	10116
rs748744787	snp	G/T			utr-variant-5-prime, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278205	TTCCTCCCTGCGCGG[G/T]CTGGGTCGCGGACGT	10116
rs748781328	snp	A/G			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68291681	AACATTAAGAGGAAT[A/G]GGATATCCAGGTGTT	10116
rs748786453	snp	A/C			missense	FEM1B	GRCh38.p7	15:68290273	TGCTTATGGGAATAG[A/C]ACTGAATGTAGAAAT	10116
rs748839135	snp	A/G	5.26422e-05	0.00513014	synonymous-codon	FEM1B	GRCh38.p7	15:68291224	CAGAACTCTTGAAGA[A/G]TTTGTTGGATTTCAT	10116
rs748841725	in-del	-/TCTATA			cds-indel	FEM1B	GRCh38.p7	15:68293844	TAAGAAAATGATAGT[-/TCTATA]TCTCAGCCCTCTGTG	10116
rs748961956	in-del	-/CCCAT			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68295533	CCCTGTCCTTTTCAC[-/CCCAT]CCTGCAATCCTCCGT	10116
rs749232785	snp	A/G			intron-variant	FEM1B	GRCh38.p7	15:68285462	AAAGTTCAACAACCA[A/G]ATTACATTCCTACTT	10116
rs749233078	snp	A/G	1.65184e-05	0.00287384	synonymous-codon, utr-variant-5-prime	FEM1B	GRCh38.p7	15:68289664	AGCAGGACATTTTGA[A/G]GTTGTTAAACTTCTA	10116
rs749307890	snp	A/G			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68295039	TGGGCTGGGTTATAC[A/G]GCATGCCCTCCCCCA	10116
rs749413928	snp	C/T	1.64991e-05	0.00287215	synonymous-codon	FEM1B	GRCh38.p7	15:68290534	ATTTGCTCAAGTTTT[C/T]TCACAAATGATACAT	10116
rs749441709	snp	A/G			upstream-variant-2KB	FEM1B	GRCh38.p7	15:68276967	TCACCCAAACTAAAT[A/G]AGTGCCCCCATCATT	10116
rs749448338	in-del	-/T			intron-variant	FEM1B	GRCh38.p7	15:68282407	TCATGTAATACATGA[-/T]TTTTTAAGGACTTTG	10116
rs749576410	snp	A/C			intron-variant	FEM1B	GRCh38.p7	15:68283639	TGATTGTGCCACTGT[A/C]CTTAGCCGGTACAAC	10116
rs750001867	snp	C/T			upstream-variant-2KB	FEM1B	GRCh38.p7	15:68276549	TGAGTTTTTTGAGAC[C/T]GTCCCAGAAGCTTCA	10116
rs750099001	in-del	-/AT	2.12121e-05	0.00325662	intron-variant	FEM1B	GRCh38.p7	15:68289554	ATACATCCCTTAAAC[-/AT]ATGTTAGGCTGTGGC	10116
rs750134925	snp	A/T	1.66693e-05	0.00288693	missense	FEM1B	GRCh38.p7	15:68289912	CCAATGCCAAAGCAC[A/T]TTGTGGAGCCACAGC	10116
rs750301832	snp	C/T			intron-variant	FEM1B	GRCh38.p7	15:68281656	GGAGTCTCGCTCTGT[C/T]GCCGGGGCTGGAGTG	10116
rs750340461	snp	G/T	1.64898e-05	0.00287135	missense	FEM1B	GRCh38.p7	15:68290076	GTAGAACTGTTACTC[G/T]CTCATGCTGATTGCG	10116
rs750604592	snp	C/T	1.64928e-05	0.00287161	missense	FEM1B	GRCh38.p7	15:68291085	AACAGAATAAGACTC[C/T]GCTAGACAAAAGTAC	10116
rs750666942	in-del	-/AA			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68294555	AGCTACTTTATGAAT[-/AA]AAGACCACTTTGGGT	10116
rs750939676	snp	A/G			upstream-variant-2KB	FEM1B	GRCh38.p7	15:68275937	TTGGCAGAGGAGAGG[A/G]AGGGTGGTAGGGAGA	10116
rs751042625	snp	G/T	1.65627e-05	0.00287769	missense, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278548	TCAGCCAGCAGGGAG[G/T]GCAGCGCTCCACGCC	10116
rs751070328	snp	A/G			intron-variant	FEM1B	GRCh38.p7	15:68281743	CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC	10116
rs751140114	in-del	-/AA			intron-variant	FEM1B	GRCh38.p7	15:68280178	TCTTTTTCAGTCGTC[-/AA]AGAGATGTTTTGAGG	10116
rs751162214	snp	G/T			downstream-variant-500B	FEM1B	GRCh38.p7	15:68296066	AGAGACAATCACTAT[G/T]AATAGTTTTTTGAGT	10116
rs751178175	snp	G/T			intron-variant	FEM1B	GRCh38.p7	15:68280606	ACATGAAGAAGAGGG[G/T]CAGCAGCTTGGTGCC	10116
rs751270545	snp	A/G			intron-variant	FEM1B	GRCh38.p7	15:68282988	CATAGAATATCTTTA[A/G]AATTTTTAATTGCCT	10116
rs751308243	snp	A/G	1.64933e-05	0.00287165	missense	FEM1B	GRCh38.p7	15:68290205	TTAGCCATGTTAGAG[A/G]GGTTCCAAGATGGTG	10116
rs751332836	snp	C/T			synonymous-codon, utr-variant-5-prime	FEM1B	GRCh38.p7	15:68289610	TTTCATGTGTAGGTA[C/T]GTCATTGATGGTGCC	10116
rs751466645	in-del	-/CT			intron-variant	FEM1B	GRCh38.p7	15:68288898	GTTTACTAGAGTCCC[-/CT]TTGTGCTTTCTCCCA	10116
rs751519168	in-del	-/A/C			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68295360	TTGTATCTATTTTTT[-/A/C]ATCAGGTGTTGTAAA	10116
rs751697708	snp	C/T	1.67579e-05	0.00289459	intron-variant, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278671	GCTTCGACGGGTAGG[C/T]ACATCCCAAGCCAGC	10116
rs751807595	snp	C/G			intron-variant	FEM1B	GRCh38.p7	15:68286408	TAGAGAGAGGTTCTC[C/G]CACTGTTGCTCAGGC	10116
rs751824133	snp	A/G	0.000232266	0.010774	intron-variant	FEM1B	GRCh38.p7	15:68289554	ATACATCCCTTAAAC[A/G]TATGTTAGGCTGTGG	10116
rs751898145	snp	C/T			intron-variant	FEM1B	GRCh38.p7	15:68286499	ACACACACACACACA[C/T]ATACCACACAACCTG	10116
rs752018023	snp	C/T			upstream-variant-2KB	FEM1B	GRCh38.p7	15:68276004	AAGGCAGAGAGGAGA[C/T]AGATGGTAGATGAGG	10116
rs752123071	snp	C/T	1.64904e-05	0.00287139	missense	FEM1B	GRCh38.p7	15:68290658	TCAGATGCTGATGTC[C/T]ACAATGCTATGGACA	10116
rs752310700	snp	C/T			intron-variant	FEM1B	GRCh38.p7	15:68283339	TTGAAGTAGTTTAGA[C/T]TCCTGTTTCCTGGCA	10116
rs752405463	snp	A/G			downstream-variant-500B	FEM1B	GRCh38.p7	15:68296031	TTTTCATCTCTCCCC[A/G]CCTCCTATTTGGACT	10116
rs752447501	snp	C/T			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68293150	GCAACTCTCAGTGGC[C/T]TGAAAGAGAAAATGC	10116
rs752638042	in-del	-/AG			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68293537	GATTGAAATGCTGAC[-/AG]AGGGTGGAGAACGAA	10116
rs752938528	snp	A/G	1.67036e-05	0.0028899	missense	FEM1B	GRCh38.p7	15:68289888	ACCTTTTAGAACAAC[A/G]TGCTGATCCCAATGC	10116
rs752953381	snp	C/G			downstream-variant-500B	FEM1B	GRCh38.p7	15:68296312	ATTGATGGACTTTTA[C/G]ATTTTCAGTTTTTGA	10116
rs752980430	snp	A/G			upstream-variant-2KB	FEM1B	GRCh38.p7	15:68276919	CCTAGAATACCGTCT[A/G]TTCTTGTCACTTGTC	10116
rs753338246	snp	C/T	1.64846e-05	0.0028709	missense	FEM1B	GRCh38.p7	15:68290431	TTTATGCGGATAATA[C/T]GGAATTTGAGCAGTG	10116
rs753416814	snp	A/G			intron-variant	FEM1B	GRCh38.p7	15:68286060	GTCTCTAATTTTTGT[A/G]TGTACTGTGAGGTAG	10116
rs753724678	snp	C/T			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68294579	TTTGGGTTATTTAAG[C/T]AGAAGCGTTTCTTTT	10116
rs753784214	snp	G/T			upstream-variant-2KB	FEM1B	GRCh38.p7	15:68276274	ACTCGTGTTTCTGTA[G/T]GGATCTGCAATAAGT	10116
rs753839082	snp	C/T	1.6703e-05	0.00288985	missense	FEM1B	GRCh38.p7	15:68289903	GTGCTGATCCCAATG[C/T]CAAAGCACATTGTGG	10116
rs753925908	snp	C/G	3.29473e-05	0.00405864	missense	FEM1B	GRCh38.p7	15:68290961	AATGAGGGAAACAGT[C/G]CCCTTCATATTATCG	10116
rs753926574	snp	C/T			intron-variant	FEM1B	GRCh38.p7	15:68289476	AATTACCTGTTTTTA[C/T]TTTCATGAGAACTGA	10116
rs754065123	snp	C/G	1.64741e-05	0.00286998	synonymous-codon	FEM1B	GRCh38.p7	15:68290939	TGCTGAGGTGAATGC[C/G]GTGGACAATGAGGGA	10116
rs754184266	snp	C/T	1.85348e-05	0.00304419	synonymous-codon, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278438	GGGCCTGGCTGGCTA[C/T]GTATACAAGGCGGCC	10116
rs754251114	in-del	-/A			upstream-variant-2KB	FEM1B	GRCh38.p7	15:68277351	TTCCAGTCCCTTCTC[-/A]AGAGCCTGGTGTTGT	10116
rs754301466	snp	A/T			intron-variant	FEM1B	GRCh38.p7	15:68283641	ATTGTGCCACTGTAC[A/T]TAGCCGGTACAACAG	10116
rs754498471	snp	A/G			intron-variant	FEM1B	GRCh38.p7	15:68279194	GCAGCATCATGAGGG[A/G]TTGTCACGCAGCCAG	10116
rs754622000	snp	A/G			intron-variant	FEM1B	GRCh38.p7	15:68280786	ATCTCAAATGTTTCC[A/G]TCATTTAAGATTTCA	10116
rs754779164	snp	A/G	3.31895e-05	0.00407353	synonymous-codon	FEM1B	GRCh38.p7	15:68289841	CTGCCTAATGATTGC[A/G]GCATATAAGGGACAC	10116
rs754859235	snp	G/T			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68295842	AAATGGTGTTTGTGT[G/T]CAGTAAATGTTTGAA	10116
rs754920588	snp	C/T			intron-variant, utr-variant-5-prime	FEM1B	GRCh38.p7	15:68278811	TGCCCCACTAATGCC[C/T]ACTTCATCTTCCAGG	10116
rs754936165	snp	C/T			utr-variant-5-prime, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68277983	CTTAGGCCGGGTGGG[C/T]CGGGTCAGGAGAGAC	10116
rs754972176	snp	C/T			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68291316	CAGACAGTAGAATTA[C/T]GTGTTCATAAATTCT	10116
rs755018325	in-del	-/AACAT			intron-variant	FEM1B	GRCh38.p7	15:68286792	AATCATGACAATAAA[-/AACAT]AACATAACAAAAAAA	10116
rs755130217	snp	A/T			upstream-variant-2KB	FEM1B	GRCh38.p7	15:68276012	GAGGAGACAGATGGT[A/T]GATGAGGTGCATGCT	10116
rs755222191	snp	C/G			intron-variant	FEM1B	GRCh38.p7	15:68286416	GGTTCTCGCACTGTT[C/G]CTCAGGCAAGAGTGC	10116
rs755398901	snp	C/T			upstream-variant-2KB	FEM1B	GRCh38.p7	15:68276809	ATCTATCATTCTTAC[C/T]GTGGCCCACTCTGCT	10116
rs755443852	snp	A/G	3.29766e-05	0.00406045	missense	FEM1B	GRCh38.p7	15:68290669	TGTCCACAATGCTAT[A/G]GACAATTATGAATGT	10116
rs755561777	snp	A/G			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68294810	TTTCTCACTGACTAT[A/G]TAACATTAAAAAGGG	10116
rs755637386	snp	A/G	8.24695e-05	0.0064209	missense	FEM1B	GRCh38.p7	15:68290232	GGTGATAACATTCTC[A/G]AAAAAGAGGTTCTTC	10116
rs755726730	snp	A/G	1.64838e-05	0.00287083	missense	FEM1B	GRCh38.p7	15:68290427	GCTGTTTATGCGGAT[A/G]ATATGGAATTTGAGC	10116
rs755732277	snp	A/T			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68291559	TATAATTTCAAGTTG[A/T]TAATGTTTTAAACAG	10116
rs755922689	snp	A/C			intron-variant, utr-variant-5-prime	FEM1B	GRCh38.p7	15:68278876	TCATCAGCCCCTACC[A/C]CTCATTCCCTCTGTG	10116
rs755924740	snp	G/T			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68293179	GCACTTCTTCAAGGT[G/T]AGTGAATCATGCTTT	10116
rs756082611	snp	C/T	6.6798e-05	0.0057788	intron-variant, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278686	TACATCCCAAGCCAG[C/T]CTCTCTCCGACGCGC	10116
rs756197087	snp	A/G			intron-variant	FEM1B	GRCh38.p7	15:68289389	GGGTTATATACTCTA[A/G]TAGTAACAGTAATAG	10116
rs756242139	snp	A/G	1.86045e-05	0.0030499	intron-variant	FEM1B	GRCh38.p7	15:68289586	CTCTGTTATCTAACT[A/G]CTTATTCTTTTCATG	10116
rs756282009	snp	A/G			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68292828	GGCCTTAAATAAAAT[A/G]GAGATACCCCACAAA	10116
rs756406918	snp	A/C	4.94515e-05	0.00497225	missense	FEM1B	GRCh38.p7	15:68290688	AATTATGAATGTAAT[A/C]TCTATACCTTTCTGT	10116
rs756558254	snp	A/G			intron-variant	FEM1B	GRCh38.p7	15:68283406	CAGTGGCTCACACCT[A/G]TAATCCCAGCACTTT	10116
rs756580056	snp	C/G	3.76166e-05	0.00433669	synonymous-codon, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278435	GGAGGGCCTGGCTGG[C/G]TATGTATACAAGGCG	10116
rs756658552	snp	C/T			intron-variant	FEM1B	GRCh38.p7	15:68281418	TTCTTAGCTTCATCC[C/T]ATGTAATTATGGGTT	10116
rs756709306	snp	C/T			intron-variant	FEM1B	GRCh38.p7	15:68281907	GCTTGAGCCACTGTG[C/T]GCGGCCTCTTGTTCA	10116
rs756806236	snp	A/G	9.88989e-05	0.00703134	synonymous-codon	FEM1B	GRCh38.p7	15:68290456	GCAGTGTATCAAGTT[A/G]TGGCTTCATGCCCTG	10116
rs756839355	snp	C/T			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68294624	GGGTGGGATGAGGAG[C/T]GAGTTGCCAGACCTT	10116
rs757001949	snp	A/G			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68293342	AAAACTTAAAATATC[A/G]GATAATGTTGCATGT	10116
rs757037936	snp	A/G			intron-variant	FEM1B	GRCh38.p7	15:68280408	GATGTCAGTCTGGGT[A/G]GGGGGAGAGAAATTA	10116
rs757074864	snp	C/T	1.67005e-05	0.00288963	synonymous-codon	FEM1B	GRCh38.p7	15:68289904	TGCTGATCCCAATGC[C/T]AAAGCACATTGTGGA	10116
rs757124718	in-del	-/A			intron-variant	FEM1B	GRCh38.p7	15:68280627	GCTTGGTGCCCTTGC[-/A]GTGACTAGTGTTTCA	10116
rs757136767	snp	C/T			upstream-variant-2KB	FEM1B	GRCh38.p7	15:68277301	CCCATCTTTCTCTCA[C/T]ACTTAACCCCTTTCT	10116
rs757277752	in-del	-/TTCTC			intron-variant	FEM1B	GRCh38.p7	15:68289019	TTCATCTGACTTCTT[-/TTCTC]AGCATCAGGTTTATG	10116
rs757432489	snp	A/G	1.64743e-05	0.00287	missense	FEM1B	GRCh38.p7	15:68290940	GCTGAGGTGAATGCC[A/G]TGGACAATGAGGGAA	10116
rs757540393	snp	A/G	7.33003e-05	0.00605349	synonymous-codon, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278441	CCTGGCTGGCTATGT[A/G]TACAAGGCGGCCAGC	10116
rs757594246	snp	A/G	1.64855e-05	0.00287097	missense	FEM1B	GRCh38.p7	15:68291075	ATGACGAATAAACAG[A/G]ATAAGACTCCGCTAG	10116
rs757641402	snp	C/G			intron-variant	FEM1B	GRCh38.p7	15:68283656	TTAGCCGGTACAACA[C/G]AGCAAGACCCTGTTT	10116
rs758007621	snp	C/T			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68294751	AGAATCTTAAATGTT[C/T]CTTTTCAAATTAGAT	10116
rs758058919	in-del	-/CTAA			intron-variant	FEM1B	GRCh38.p7	15:68289579	TGTGGCCTCTGTTAT[-/CTAA]CTAACTGCTTATTCT	10116
rs758186768	snp	C/T	6.667e-05	0.00577326	synonymous-codon	FEM1B	GRCh38.p7	15:68289913	CAATGCCAAAGCACA[C/T]TGTGGAGCCACAGCA	10116
rs758259773	in-del	-/T			intron-variant	FEM1B	GRCh38.p7	15:68281783	AACCATGCCTGGCTA[-/T]TTTTTTGTATTTTTA	10116
rs758369187	snp	A/G			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68293430	CTTATTTATAAAATG[A/G]GAATAATGATTATAT	10116
rs758414083	in-del	-/CAAA			intron-variant	FEM1B	GRCh38.p7	15:68285766	TTGAACTCTTAGGTT[-/CAAA]CAAACAGTCCTCTTC	10116
rs758563201	snp	C/G	3.29826e-05	0.00406082	missense	FEM1B	GRCh38.p7	15:68291092	TAAGACTCCGCTAGA[C/G]AAAAGTACAACTGGG	10116
rs758640118	snp	C/T	1.66065e-05	0.00288149	synonymous-codon, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278654	GCAGACTGGCACCGT[C/T]CGCTTCGACGGGTAG	10116
rs758866923	snp	C/T			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68295222	ATCTTGATGTGTGTA[C/T]AGGGGTAAGTATTGC	10116
rs758932225	snp	C/T	1.6486e-05	0.00287102	synonymous-codon	FEM1B	GRCh38.p7	15:68290270	CCATGCTTATGGGAA[C/T]AGAACTGAATGTAGA	10116
rs759127129	snp	C/T	1.6552e-05	0.00287676	missense, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278622	TTGCTCTTAGAACAT[C/T]ACCGGGTGCAGACTC	10116
rs759248903	snp	A/G			intron-variant	FEM1B	GRCh38.p7	15:68284647	CACTTTATCACTCTA[A/G]AAGTTTCCCTTGTGC	10116
rs759357686	in-del	-/G			downstream-variant-500B	FEM1B	GRCh38.p7	15:68296010	ATATATATTTTAAAA[-/G]TTCCCTTTTCATCTC	10116
rs759411118	snp	C/T	1.65037e-05	0.00287256	synonymous-codon	FEM1B	GRCh38.p7	15:68290549	CTCACAAATGATACA[C/T]TTGAATGAAACTGTG	10116
rs759561935	snp	C/T			utr-variant-5-prime, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278380	GCACGGCAGCTGCAG[C/T]GGTGGCGACCAAACG	10116
rs759653999	snp	A/G			intron-variant	FEM1B	GRCh38.p7	15:68281385	ATTTGCTTGATAGTT[A/G]TCTTCAGAATGTTTT	10116
rs759742414	snp	C/T			intron-variant	FEM1B	GRCh38.p7	15:68279626	CTGAGCATAAAAATA[C/T]ATATCTTTAGTTTTT	10116
rs759759344	snp	A/G			upstream-variant-2KB	FEM1B	GRCh38.p7	15:68277621	GTCAAGGACATTGAG[A/G]ACATCCAGGCCCAAA	10116
rs759829239	snp	A/G	1.6684e-05	0.00288821	synonymous-codon	FEM1B	GRCh38.p7	15:68289886	ATACCTTTTAGAACA[A/G]CGTGCTGATCCCAAT	10116
rs759860096	snp	A/G	4.94792e-05	0.00497365	synonymous-codon	FEM1B	GRCh38.p7	15:68290003	TGCTGCTATAGTAGT[A/G]AATGGCCATGGGATG	10116
rs759901104	in-del	-/AGGG			upstream-variant-2KB	FEM1B	GRCh38.p7	15:68276502	TTTGTCCTTTGGGGA[-/AGGG]AGGAAGAGGGAGGAA	10116
rs759924854	snp	C/T			missense	FEM1B	GRCh38.p7	15:68290698	GTAATCTCTATACCT[C/T]TCTGTATTTAGTGTG	10116
rs760133837	in-del	-/ATATC			intron-variant	FEM1B	GRCh38.p7	15:68284529	TTTTTTAGTGGAGGT[-/ATATC]ATATCTAGTAAAGTA	10116
rs760249163	snp	A/G			intron-variant	FEM1B	GRCh38.p7	15:68285563	TTGTTAAATTTAGCT[A/G]TTCTGCTGGGTGTGT	10116
rs760265671	snp	A/G			intron-variant	FEM1B	GRCh38.p7	15:68284822	GCAGGTCTTTCCCGT[A/G]CTGTTCTCTTGATAG	10116
rs760453726	snp	A/G			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68294425	AACATTGTTTGAAGT[A/G]AAATATGATTTGGGG	10116
rs760518376	snp	C/T			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68295506	TCTGACTGGCCTAAT[C/T]GATGGAAAAGACCCT	10116
rs760568108	snp	A/C			upstream-variant-2KB	FEM1B	GRCh38.p7	15:68276203	CGCTACCAGTAGAAT[A/C]TTACCTTCAGCCCTT	10116
rs760646274	snp	A/G	1.66649e-05	0.00288655	utr-variant-5-prime, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278367	GGCCTCCGGGGGCGC[A/G]CGGCAGCTGCAGCGG	10116
rs760904212	snp	C/T	0.000133547	0.00817041	synonymous-codon	FEM1B	GRCh38.p7	15:68289892	TTTAGAACAACGTGC[C/T]GATCCCAATGCCAAA	10116
rs760922686	snp	C/T	1.64925e-05	0.00287158	synonymous-codon	FEM1B	GRCh38.p7	15:68290025	CATGGGATGACGCCA[C/T]TGAAAGTAGCTGCCG	10116
rs761022409	snp	A/C	1.64727e-05	0.00286986	missense	FEM1B	GRCh38.p7	15:68291055	AAGCCGGAGCTCACA[A/C]TGACATGACGAATAA	10116
rs761074123	snp	A/G			intron-variant	FEM1B	GRCh38.p7	15:68279187	AGCAGCTGCAGCATC[A/G]TGAGGGATTGTCACG	10116
rs761110543	snp	C/G	1.65614e-05	0.00287757	missense, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278550	AGCCAGCAGGGAGGG[C/G]AGCGCTCCACGCCCC	10116
rs761162059	snp	A/C			missense, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278538	CTTGGCTATGTCAGC[A/C]AGCAGGGAGGGCAGC	10116
rs761166179	snp	A/G			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68292555	ATGAAAGCAAAATTA[A/G]CTGTATCTGTAATTT	10116
rs761169628	snp	C/T			upstream-variant-2KB	FEM1B	GRCh38.p7	15:68276348	CCACACCTCCACCAA[C/T]AGCTGCAATGGAAGT	10116
rs761267600	snp	G/T	1.99181e-05	0.00315574	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68291288	GTGCTAAAAAGTAAA[G/T]GACTTTTAATCACAG	10116
rs761340682	snp	A/T			intron-variant	FEM1B	GRCh38.p7	15:68287389	AGATGAAAATGTAGG[A/T]CATTTCCAGTACCTT	10116
rs761400696	snp	C/T	2.66237e-05	0.00364844	utr-variant-5-prime, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278394	GCGGTGGCGACCAAA[C/T]GGGTGTTGGAGTTGG	10116
rs761495243	snp	A/G	1.64738e-05	0.00286995	missense	FEM1B	GRCh38.p7	15:68290790	AACCTGATTCACCTT[A/G]ATCCCAGAACTCGTG	10116
rs761540507	in-del	-/ATTA			intron-variant	FEM1B	GRCh38.p7	15:68285265	GTTTATCCATTTCCT[-/ATTA]ATTAATATTTTGGTT	10116
rs761614920	snp	C/T			intron-variant	FEM1B	GRCh38.p7	15:68281473	TGAGAAAGACATACA[C/T]TAAAATAAATATTAC	10116
rs761702577	snp	C/T			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68295794	AATAACTCAGCTAAT[C/T]TGAAACTAACAATCT	10116
rs761831445	snp	A/T	1.6489e-05	0.00287128	synonymous-codon	FEM1B	GRCh38.p7	15:68290063	TAAAGCTGATGTCGT[A/T]GAACTGTTACTCTCT	10116
rs761833966	snp	C/T	0.000115307	0.00759211	synonymous-codon	FEM1B	GRCh38.p7	15:68290975	TGCCCTTCATATTAT[C/T]GTTCAGTACAACAGG	10116
rs762112500	snp	C/T			intron-variant	FEM1B	GRCh38.p7	15:68279258	TGCTCGGTGTAGATA[C/T]ATTGGCTACTAAGAT	10116
rs762124297	snp	C/T			intron-variant	FEM1B	GRCh38.p7	15:68279851	TATCACGGGTATCAC[C/T]ATTATACACATTAAG	10116
rs762230327	snp	A/T	1.66502e-05	0.00288527	utr-variant-3-prime	FEM1B	GRCh38.p7	15:68291292	TAAAAAGTAAAGGAC[A/T]TTTAATCACAGACAG	10116
rs762248448	snp	A/G	3.31351e-05	0.00407019	synonymous-codon, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278630	AGAACATTACCGGGT[A/G]CAGACTCAGCAGACT	10116
rs762297583	snp	A/G			intron-variant	FEM1B	GRCh38.p7	15:68286122	ATCTTGTTGCTCCAT[A/G]ACTATTTATTAAAAA	10116
rs762338209	snp	G/T	0.000117072	0.00764997	intron-variant, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278705	TCTCCGACGCGCGCG[G/T]ACTCGTTAATTCACG	10116
rs762595379	snp	C/T	1.6476e-05	0.00287014	synonymous-codon	FEM1B	GRCh38.p7	15:68291023	GACCTTGCACTCCAT[C/T]ATCATTAGCCTAGTT	10116
rs762691926	in-del	-/CTAT			intron-variant	FEM1B	GRCh38.p7	15:68288460	TTCTAGCACAGTAGA[-/CTAT]CTGTCTCCAGCAAAA	10116
rs762729208	snp	A/G	1.65414e-05	0.00287583	synonymous-codon, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278600	TGGACACGCAAAGGT[A/G]GTACGCTTGCTCTTA	10116
rs762774520	snp	G/T			intron-variant	FEM1B	GRCh38.p7	15:68284402	TTGAATTGAAATTAC[G/T]TGAAATTGAAATTAC	10116
rs762868787	snp	C/T			intron-variant	FEM1B	GRCh38.p7	15:68282556	CAGAAATGTTATCTC[C/T]TATTGTGAAAAGTTT	10116
rs762888118	snp	C/T	1.64939e-05	0.0028717	missense	FEM1B	GRCh38.p7	15:68290197	ATCTATATTTAGCCA[C/T]GTTAGAGAGGTTCCA	10116
rs763253674	in-del	-/AT			intron-variant	FEM1B	GRCh38.p7	15:68286499	CACACACACACACAT[-/AT]ATACCACACAACCTG	10116
rs763344530	snp	A/G	2.11499e-05	0.00325185	intron-variant	FEM1B	GRCh38.p7	15:68289552	GAATACATCCCTTAA[A/G]CATATGTTAGGCTGT	10116
rs763535044	in-del	-/AAAAAAAAAA			intron-variant	FEM1B	GRCh38.p7	15:68283503	ACCTCATCTCTACCT[-/AAAAAAAAAA]AAAAAAAAAAAAAAA	10116
rs763542049	snp	A/G	1.64844e-05	0.00287087	missense	FEM1B	GRCh38.p7	15:68290430	GTTTATGCGGATAAT[A/G]TGGAATTTGAGCAGT	10116
rs763598515	snp	A/G			intron-variant	FEM1B	GRCh38.p7	15:68283437	GGGAGGCCTAGGTGG[A/G]GATATCATTTGAGCT	10116
rs763605572	snp	C/G			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68291880	AATTGTTGCATTATG[C/G]TGGGTAGTATATACA	10116
rs763628417	in-del	-/T			intron-variant	FEM1B	GRCh38.p7	15:68284557	TAAAGTACATGAATC[-/T]TGTGTACAATACTGT	10116
rs763668304	snp	A/G			intron-variant	FEM1B	GRCh38.p7	15:68286025	TTTGAGAAGCTTTTC[A/G]CACTATAGGTCTATA	10116
rs763808050	snp	G/T	2.80761e-05	0.00374663	utr-variant-5-prime, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278381	CACGGCAGCTGCAGC[G/T]GTGGCGACCAAACGG	10116
rs763865567	snp	A/G			upstream-variant-2KB	FEM1B	GRCh38.p7	15:68275870	GGAGATGGTTTTTCT[A/G]AAGAGCCAGGCACTC	10116
rs764071267	snp	A/G			intron-variant	FEM1B	GRCh38.p7	15:68280294	CAGAGAAATTAATGA[A/G]TTCGGTAAGTAAACA	10116
rs764142515	snp	A/C			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68295602	ACTGTGATTTATAAC[A/C]AACCGGTGATGTCAT	10116
rs764256411	snp	A/G	8.35164e-05	0.00646152	missense	FEM1B	GRCh38.p7	15:68289893	TTAGAACAACGTGCT[A/G]ATCCCAATGCCAAAG	10116
rs764266300	snp	A/G			intron-variant	FEM1B	GRCh38.p7	15:68289429	ATTGAGCTTTATATT[A/G]GGTACAAGTACTATG	10116
rs764272821	snp	G/T	1.64906e-05	0.00287142	missense	FEM1B	GRCh38.p7	15:68290055	GAAAGCTGTAAAGCT[G/T]ATGTCGTAGAACTGT	10116
rs764372616	snp	A/G	1.65663e-05	0.002878	missense, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278542	GCTATGTCAGCCAGC[A/G]GGGAGGGCAGCGCTC	10116
rs764398817	in-del	-/T			intron-variant	FEM1B	GRCh38.p7	15:68285692	TATACTTGTTCAGTC[-/T]TTTTTTTTTTTTCTT	10116
rs764459828	snp	G/T			intron-variant	FEM1B	GRCh38.p7	15:68284848	GATAGTAAGTGTCAC[G/T]GGATCTGATGATTGT	10116
rs764464606	snp	A/G			missense	FEM1B	GRCh38.p7	15:68290947	TGAATGCCGTGGACA[A/G]TGAGGGAAACAGTGC	10116
rs764474695	snp	A/G/T	4.94599e-05	0.00497272	synonymous-codon	FEM1B	GRCh38.p7	15:68291065	TCACACTGACATGAC[A/G/T]AATAAACAGAATAAG	10116
rs764568921	snp	C/T			intron-variant	FEM1B	GRCh38.p7	15:68279216	CGCAGCCAGACATCT[C/T]AAGACATGATTCTGA	10116
rs764711464	snp	C/G/T	3.31133e-05	0.00406887	synonymous-codon, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278555	GCAGGGAGGGCAGCG[C/G/T]TCCACGCCCCTCATC	10116
rs764729391	snp	C/G			upstream-variant-2KB	FEM1B	GRCh38.p7	15:68276515	GAAGGGAGGAAGAGG[C/G]AGGAAGTCACTTTCA	10116
rs764842630	snp	A/G	4.94214e-05	0.00497074	missense	FEM1B	GRCh38.p7	15:68290803	TTGATCCCAGAACTC[A/G]TGAAGGTTTCACCTT	10116
rs764985259	snp	C/G			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68294733	TATGATAGATTTTCT[C/G]TAAGAATCTTAAATG	10116
rs765302188	in-del	-/TTCA			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68294354	TGAGAAGGGTTTTAT[-/TTCA]TTCATTATACTAATA	10116
rs765351213	snp	C/G	1.64942e-05	0.00287173	missense	FEM1B	GRCh38.p7	15:68290184	AAGACATACCACTAT[C/G]TATATTTAGCCATGT	10116
rs765353250	snp	C/T			intron-variant, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278723	TCGTTAATTCACGGG[C/T]CCTCCCCTCCCTCAC	10116
rs765481777	snp	A/T	1.64898e-05	0.00287135	synonymous-codon	FEM1B	GRCh38.p7	15:68291083	TAAACAGAATAAGAC[A/T]CCGCTAGACAAAAGT	10116
rs765680142	snp	C/G	1.67545e-05	0.0028943	intron-variant, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278709	CGACGCGCGCGGACT[C/G]GTTAATTCACGGGCC	10116
rs765694329	snp	A/G			upstream-variant-2KB	FEM1B	GRCh38.p7	15:68275935	TGTTGGCAGAGGAGA[A/G]GGAGGGTGGTAGGGA	10116
rs765742295	in-del	-/T			intron-variant	FEM1B	GRCh38.p7	15:68285902	AAATCCAATAAATAC[-/T]TTTCTTTTTCTTTAA	10116
rs765769539	in-del	-/AAGT			intron-variant	FEM1B	GRCh38.p7	15:68281252	AACAGCTGTGTGCTG[-/AAGT]AAGTAGATTAGTGTT	10116
rs765784335	snp	C/G			intron-variant	FEM1B	GRCh38.p7	15:68286183	GCCTTTGTCAGAAAT[C/G]AAGGGATTCTGTATG	10116
rs765970150	snp	G/T			downstream-variant-500B	FEM1B	GRCh38.p7	15:68296040	CTCCCCGCCTCCTAT[G/T]TGGACTCTGCAGAGA	10116
rs766038209	snp	C/T			missense, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278553	CAGCAGGGAGGGCAG[C/T]GCTCCACGCCCCTCA	10116
rs766077199	snp	A/G			intron-variant	FEM1B	GRCh38.p7	15:68282809	CAGTATAGTCTTACA[A/G]TTTTAGCTAGATTTT	10116
rs766133819	in-del	-/TTGA			intron-variant	FEM1B	GRCh38.p7	15:68288739	TTTTTCCTGTAGTGG[-/TTGA]TTGATTGAGGAACAC	10116
rs766196005	snp	C/T	1.64942e-05	0.00287173	synonymous-codon	FEM1B	GRCh38.p7	15:68290199	CTATATTTAGCCATG[C/T]TAGAGAGGTTCCAAG	10116
rs766357393	snp	C/G	1.64841e-05	0.00287085	missense	FEM1B	GRCh38.p7	15:68290399	TGTTTCTCATCCCAT[C/G]ATTTACAGAGGAGCT	10116
rs766550983	snp	C/T			upstream-variant-2KB	FEM1B	GRCh38.p7	15:68275967	ACGGAGTTAGAGATA[C/T]GGAGAGACAGAGAGA	10116
rs766644809	snp	C/T			intron-variant	FEM1B	GRCh38.p7	15:68289553	AATACATCCCTTAAA[C/T]ATATGTTAGGCTGTG	10116
rs766669511	snp	A/G	1.66599e-05	0.00288611	splice-donor-variant, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278666	CGTCCGCTTCGACGG[A/G]TAGGTACATCCCAAG	10116
rs766761555	snp	C/T			intron-variant	FEM1B	GRCh38.p7	15:68288038	TTTCACCATGTTGGC[C/T]AGGCTCGTCTTGAAC	10116
rs766916243	snp	C/T			upstream-variant-2KB	FEM1B	GRCh38.p7	15:68276712	CCTCTTTAAAACCCT[C/T]CAAATGCCCCCATCA	10116
rs766931623	snp	C/T			intron-variant	FEM1B	GRCh38.p7	15:68283227	ATCACTTTTTGTCTC[C/T]TTTCATCTCTAAAAT	10116
rs766933648	snp	C/T	1.65545e-05	0.00287697	synonymous-codon, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278624	GCTCTTAGAACATTA[C/T]CGGGTGCAGACTCAG	10116
rs766963544	in-del	-/TC			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68291970	TTGAATTCTTCAAAG[-/TC]TATTTTAATGAAATT	10116
rs767201907	snp	C/T	1.64939e-05	0.0028717	synonymous-codon	FEM1B	GRCh38.p7	15:68290225	CCAAGATGGTGATAA[C/T]ATTCTCGAAAAAGAG	10116
rs767246262	snp	C/G			intron-variant	FEM1B	GRCh38.p7	15:68284689	TTCCTCCCTTTCCTT[C/G]CCAGAGGTAATGATT	10116
rs767331756	snp	C/T	1.64844e-05	0.00287087	missense	FEM1B	GRCh38.p7	15:68290422	GAGGAGCTGTTTATG[C/T]GGATAATATGGAATT	10116
rs767436234	snp	A/G			intron-variant	FEM1B	GRCh38.p7	15:68279286	GATGGCATTGGACCT[A/G]ATGTGGGAGATGATG	10116
rs767482251	snp	C/T			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68292960	TTCAGTTAGGAAGGT[C/T]TTGATGGTAAATTCT	10116
rs767589043	in-del	-/C			intron-variant	FEM1B	GRCh38.p7	15:68288407	GAATATTCCTTTGAT[-/C]CAACCTTTCTTCTTA	10116
rs767669277	snp	C/T	5.84311e-05	0.00540483	intron-variant	FEM1B	GRCh38.p7	15:68289580	TGTGGCCTCTGTTAT[C/T]TAACTGCTTATTCTT	10116
rs767682173	snp	C/T	0.000116929	0.00764531	missense	FEM1B	GRCh38.p7	15:68289887	TACCTTTTAGAACAA[C/T]GTGCTGATCCCAATG	10116
rs767799750	snp	C/T			intron-variant	FEM1B	GRCh38.p7	15:68289253	GAACATGCTGTTCTC[C/T]TAGTAACCAGTGAAT	10116
rs767891756	snp	C/T			intron-variant	FEM1B	GRCh38.p7	15:68288146	AACGCCTCTTGTGTG[C/T]GGTCCTTAATTTCAT	10116
rs767988389	in-del	-/ATG			cds-indel	FEM1B	GRCh38.p7	15:68294405	TGTGAGAACTTAGGT[-/ATG]ATAACATTGTTTGAA	10116
rs768111476	snp	C/T	1.64741e-05	0.00286998	synonymous-codon	FEM1B	GRCh38.p7	15:68290852	TTCCAATACTCCAGT[C/T]GATGATTTCCACACC	10116
rs768172728	snp	A/G			upstream-variant-2KB	FEM1B	GRCh38.p7	15:68277583	CCTCAGGGCCGTTTA[A/G]GGGCCAGGAGGAGGT	10116
rs768330591	snp	A/T	1.64741e-05	0.00286998	missense	FEM1B	GRCh38.p7	15:68290751	AGCGAAGAAGATCAG[A/T]GCAAAATTAACAAGC	10116
rs768506639	snp	C/T	8.23621e-05	0.00641672	synonymous-codon	FEM1B	GRCh38.p7	15:68290987	TATCGTTCAGTACAA[C/T]AGGCCCATCAGTGAT	10116
rs768520107	snp	C/T			upstream-variant-2KB	FEM1B	GRCh38.p7	15:68277404	TCGGGAACTCAGAAA[C/T]GCCGCCCTTTTCCTG	10116
rs768528246	in-del	-/ACAACCTGATTC	1.64749e-05	0.00287005	cds-indel	FEM1B	GRCh38.p7	15:68290772	TTAACAAGCAGATCT[-/ACAACCTGATTC]ACAACCTGATTCACC	10116
rs768595497	snp	C/G	1.66291e-05	0.00288345	missense, upstream-variant-2KB	FEM1B	GRCh38.p7	15:68278508	AACCGGTCTGAAAGC[C/G]ACATCCGCTATCTGC	10116
rs768622802	snp	G/T			intron-variant	FEM1B	GRCh38.p7	15:68284527	GTTTTTTTAGTGGAG[G/T]TATATCATATCTAGT	10116
rs768790046	snp	A/G			intron-variant	FEM1B	GRCh38.p7	15:68285434	CTAACAGATATTGCC[A/G]AATAGTTTCCCCAAA	10116
rs768885930	snp	A/T			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68292569	AGCTGTATCTGTAAT[A/T]TTCTCTCTAGTGCCA	10116
rs768950392	snp	A/G	1.6492e-05	0.00287154	missense	FEM1B	GRCh38.p7	15:68290163	CGTGAGAACTATGAC[A/G]TCATAAAGACATACC	10116
rs769109903	snp	C/T	1.64792e-05	0.00287042	missense	FEM1B	GRCh38.p7	15:68290310	GAACTGGAGTCCATT[C/T]GGCAAGACAGAGATG	10116
rs769250884	in-del	-/TG			utr-variant-3-prime	FEM1B	GRCh38.p7	15:68292244	TTCACTTTCTTAGTC[-/TG]TGACAAGAAGTAGAA	10116
rs769254664	snp	A/G			intron-variant	FEM1B	GRCh38.p7	15:68280817	TCTCCTTGATTCTGT[A/G]TATCAGTTTAGCTTA	10116
rs769317241	snp	A/G	1.64942e-05	0.00287173	synonymous-codon	FEM1B	GRCh38.p7	15:68290105	CGACCGAAGAAGTCG[A/G]ATTGAAGCTTTGGAA	10116
rs769342748	snp	G/T			intron-variant	FEM1B	GRCh38.p7	15:68279722	GAAATGTTCTGTTTC[G/T]GTTGATTCTTTTTTA	10116
rs769480659	in-del	-/CAAAA			intron-variant	FEM1B	GRCh38.p7	15:68283672	AGCAAGACCCTGTTT[-/CAAAA]CAAAACAAAACAAAT	10116

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