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

MINDY4

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs114473008	snp	C/T	0.02016	0.0983543	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30854988	AGAAGGAGTGCTGGC[C/T]GGGGCATCGGGAGCC	84182
rs114548263	snp	A/C	0.00874735	0.0655527	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30773609	TCTGCTGAGGTGACT[A/C]TTCTGCTGCCCCAGC	84182
rs114610780	snp	A/G	0.0123036	0.0774623	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30793379	TAGCAGGTATGTTAA[A/G]TTTTTTTTTCTAGTT	84182
rs114623966	snp	C/T	0.0543475	0.155628	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30815519	CAGGTCCAGTAGCCA[C/T]GGGCTAGTGTGCAGA	84182
rs114691213	snp	A/G	0.0111196	0.0737302	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30847379	GTAGGATGAGGGGAC[A/G]GGCCCTGCCCAAGAG	84182
rs114777754	snp	C/G	0.00676609	0.0577691	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30869128	GGTTCCTCAGGCTGT[C/G]CAGAATTCTCTGAGG	84182
rs114851856	snp	C/T	0.0146672	0.084371	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30777852	CGCCAACCCCAGATT[C/T]TCCATTGCTAGAGCA	84182
rs114877561	snp	A/C	0.0244538	0.107838	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30781920	AATAGTTGTCTTTTC[A/C]ACTCTTCCCTGAAGC	84182
rs114901555	snp	C/G	0.00676609	0.0577691	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30777061	TTCATCCAGGATGGA[C/G]TGCAGTGGTGTAATC	84182
rs114919055	snp	A/G	0.00636936	0.0560724	upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30769939	TTTAAAGAAAATAAT[A/G]CATAAGTAACTGTAT	84182
rs114979047	snp	C/T	0.00676609	0.0577691	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30814178	AAAGTATTTAATTTT[C/T]GCAAATTTTCCAAAA	84182
rs115006436	snp	C/T	0.0185938	0.0946107	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30879437	CTGAGCCATCCAGTC[C/T]GTGGTATTTGTTATG	84182
rs115045276	snp	A/C	0.00478085	0.0486577	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30773311	TGAAAGATAGGTATA[A/C]GTATTCCCTTTCACA	84182
rs115045320	snp	A/G	0.00557542	0.0525036	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30818801	TCTGTTCATTTTTTC[A/G]TCAGTTTTGTGATTT	84182
rs115057870	snp	C/T	0.0236746	0.106192	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30880837	AAGAAAGGATGAGTG[C/T]GTTGTAAAGACTGTC	84182
rs115063092	snp	A/G	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30772487	TAAGACCTACTCTTT[A/G]CAGATTTATAATGAG	84182
rs115071752	snp	A/G	0.0263992	0.111815	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30808509	TTGTGCATGTGGTGT[A/G]AGCGTGGTGTTTTGT	84182
rs115160767	snp	A/G	0.0271762	0.113356	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30861061	CACACACAGAGACAC[A/G]TAGTCCAGCTGTTCT	84182
rs115348165	snp	G/T	0.0111196	0.0737302	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30887353	GCTCCAGAAGGTCTG[G/T]TTCTGCTCCCAGCCT	84182
rs115381962	snp	A/G	0.00557542	0.0525036	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30833820	AAACAAAGGGGCCCA[A/G]GCCCTACGCAAGTCC	84182
rs115408224	snp	C/T	0.0197687	0.0974348	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30773832	ACCACATCTATATTG[C/T]ATTGTTCCTGCCAAC	84182
rs115423443	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30788912	GCATGGACATTCCTC[A/G]GTGAAGTCAGCACTT	84182
rs115610411	snp	A/C	0.00914312	0.0669923	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30860518	GCTCCTGGTTTGGCT[A/C]ATTTCTGGGCTGACG	84182
rs115657024	snp	C/G	0.00993419	0.0697739	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30878248	TGAAGCCTCTCACTT[C/G]CAGCTTGTCTCCAGG	84182
rs115755814	snp	C/G	0.0168055	0.0901129	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30866182	CAGGCCACTGAAGAG[C/G]TGGGAGGTCTCAAGA	84182
rs115761307	snp	A/G	0.0236746	0.106192	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30777966	TACCAAGAGCTTCTC[A/G]TGGGCCTGGGTCCCA	84182
rs115839118	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30830011	AGGTGAAGGATAGGA[A/G]GCCATGGAACCCAGT	84182
rs115906839	snp	C/T	0.00200372	0.0315887	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852171	GGCTGGAGGGCACGC[C/T]TTCTCTCCACTCAGA	84182
rs115932897	snp	A/C	0.0221141	0.102801	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30814359	TTTACCAGTTGAGGT[A/C]GACATAATCTTATTT	84182
rs115936558	snp	A/G	0.0248432	0.108648	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30876613	CTGAGGGGGCTGGGC[A/G]GAGGAGCACTGGACC	84182
rs116077316	snp	A/T	0.0158469	0.0875917	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30843753	GTGAGGTTTTCTATC[A/T]GTCGTTGCCGGCCAG	84182
rs116184801	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30786992	GTGTCCACCTGCGCT[C/T]TCACTTACCTGCTGT	84182
rs116345294	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30849401	CAGAATCCAAGAGAA[A/G]CCTAGAAGTACACCT	84182
rs116360995	snp	A/G	0.0267878	0.112589	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30832991	AATCTATACTGTTTT[A/G]TATGCATCATTTTTA	84182
rs116407831	snp	C/G	0.00993419	0.0697739	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30862230	CCACCTGGAGCCCAG[C/G]GGAGACTCCTGAAGA	84182
rs116645171	snp	A/C	0.0399052	0.1355	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30772028	CTTAGTCATTTTAGT[A/C]AACAGTGGGAATTCC	84182
rs116664087	snp	A/G	0.0103295	0.0711199	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30837919	CAGCCCACATTTGAT[A/G]ACATGTGGACAAATG	84182
rs116792637	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30878716	TTCATTGCCATCTTC[A/C]TGAAGGGACCCACAA	84182
rs116817026	snp	C/T	0.00478085	0.0486577	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785389	CCTCTCAGTGGTGTG[C/T]GGCAAGGCTGGGCTT	84182
rs116834997	snp	C/T	0.0225045	0.103662	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30774041	GGAGAGAAACACACA[C/T]CACTATGTTGATGGT	84182
rs116860029	snp	A/G	0.00517822	0.0506191	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30849579	TGTCCATTTGATCCT[A/G]CGACTGTGTCGTGGC	84182
rs116877098	snp	A/G	0.00676609	0.0577691	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828043	TAAAGGGAGCTTTAG[A/G]AAATGCTCCCTCAAA	84182
rs116973897	snp	A/G	0.108048	0.20579	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30846842	GAGCGCGCAACCTAG[A/G]TCCCTCGCATGCACA	84182
rs117061269	snp	A/G	0.0126979	0.078662	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30861525	TCTGGCCCTAGAGCT[A/G]GCTTTTTGGGTTTGC	84182
rs117097102	snp	A/G	0.0236746	0.106192	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30883628	TCACCTCCTTGCTGT[A/G]TTCTCTGAGTGGGCC	84182
rs117108594	snp	C/G	0.0123036	0.0774623	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30807096	AGGAAATCATGTAAA[C/G]TGAAAAAGTCCCAGA	84182
rs117158008	snp	C/T	0.00795532	0.062565	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30842474	TGCCCTCAGAGGGTA[C/T]AGGGATACTGAGCAC	84182
rs117191320	snp	A/T	0.00755907	0.0610114	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30858374	GTAGGTGCTGTGATT[A/T]TTACCCTCTTTTTAC	84182
rs117203691	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30830015	GAAGGATAGGAGGCC[A/G]TGGAACCCAGTCACG	84182
rs117251651	snp	A/C	0.0256215	0.110247	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30815550	GGGGTGGAGGTGAGA[A/C]CAAGATGAAGGGAGA	84182
rs117272384	snp	A/G	0.0225476	0.104064	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30847187	CTTACCTGTCTGATC[A/G]CTGTACTTTTTCCAA	84182
rs117298884	snp	A/C	0.00478085	0.0486577	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30826582	ACGAGGCTGGGCAGT[A/C]GGTGGCCAGATCATG	84182
rs117307510	snp	A/G	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30780353	CATTGGGCTTTTAAC[A/G]TAAATGTACCTTACC	84182
rs117410997	snp	A/G	0.00993419	0.0697739	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30861289	GGTCTCATTGCCAGC[A/G]GTAAGGATAGCGTCT	84182
rs117413863	snp	C/T	0.00557542	0.0525036	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30884185	CCCACCACAGGAAAG[C/T]GAGCCCTTGAGAGGA	84182
rs117414783	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30862697	CCAGGGAAGCCCAGT[A/G]AGGTGGCAAGTCACA	84182
rs117450876	snp	C/T	0.0298908	0.118541	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778714	TGGACAGATCCCCAG[C/T]GGGAGTGGGTTTTCC	84182
rs117479033	snp	C/T	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30799785	GCCTGAGTCAGATTC[C/T]GGTACATGTAATTTG	84182
rs117506937	snp	A/G	0.0185938	0.0946107	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30881348	TCCACAAACACTTCC[A/G]CCATGTGAAATTCCC	84182
rs117525382	snp	A/G	0.0158469	0.0875917	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30802071	TAATATTTGGGAGAT[A/G]AGTGTGAGAGAGCAG	84182
rs117622734	snp	A/C	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30842534	TTCCTTGCACTGAAA[A/C]AAATGTGCAGAGTGT	84182
rs117661071	snp	A/T	0.47517	0.10862	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30796123	TTGGAGCACTGTACT[A/T]TTTTTTTTTTTGTCT	84182
rs117707423	snp	A/G	0.00676609	0.0577691	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840289	CAGGCCACAAGTGGG[A/G]CAGAAGAGAGCGCAG	84182
rs117730741	snp	C/T	0.00398564	0.0444627	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30860026	TTAATAGCGCATGAA[C/T]GGTTGTGGAAAGTAC	84182
rs117785282	snp	A/G	0.0182019	0.0936463	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30835071	CACTTCCACATTTTC[A/G]GATATCTTTTCAGCA	84182
rs117789449	snp	A/G	0.0310518	0.120672	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30835927	CTCAGTTGTCCCACT[A/G]TGAGAAAACAATATC	84182
rs117811041	snp	G/T	0.103082	0.202275	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771788	CACGGTTTGGACCCC[G/T]TCCGCTGCCCTCCTG	84182
rs117849950	snp	C/T	0.00874735	0.0655527	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30849580	GTCCATTTGATCCTA[C/T]GACTGTGTCGTGGCA	84182
rs117858355	snp	C/T	0.000603051	0.017354	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882148	CCCTTTCCCTGGGGA[C/T]GGCATTTCACATCAG	84182
rs117858971	snp	A/G/T	0.0115144	0.0749975	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30863347	TGTATGTGTACATTC[A/G/T]TGGTGGTGTGATAGT	84182
rs117925922	snp	C/G	0.00914312	0.0669923	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839598	GGATCCTCAGCAGGA[C/G]AGAGAGCAGTAGGAG	84182
rs117937146	snp	A/G	0.0209421	0.100162	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30775813	ACAGAACAAATATAT[A/G]TTTATCATAATGTCC	84182
rs117989474	snp	C/T	0.0126979	0.078662	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828186	TTCCTTTAAACACTT[C/T]GGTGCATGTCAGAGG	84182
rs117995346	snp	C/T	0.024795	0.108548	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839338	TGCTCCTAGGTTTCC[C/T]TGGGACCTTTCTGCT	84182
rs118167873	snp	G/T	0.111928	0.208413	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30835212	TTGCACATGGCTGGG[G/T]AGGCCTCACAATCAT	84182
rs137866102	snp	C/G	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30799520	GGGCAAGGTTAAATT[C/G]CACCATCCCTAACCC	84182
rs137885882	snp	C/T	0.00597247	0.0543191	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30862593	TCTGCCTGCTGCCTC[C/T]GGGGCTAGCCGCTGG	84182
rs137931968	snp	A/G	0.00318978	0.0398085	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30802459	CCTCAGTATAGAACA[A/G]TGATTTGATAACTCA	84182
rs137967557	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30855358	AGACCTGCTGTTGAT[C/G]CGGAGTGTTGTGAGA	84182
rs137973346	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30827363	GTCCTCAGCCCTTTG[A/T]TGCAGAGCAGGCGGA	84182
rs138007779	snp	G/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30858163	TGAGGCCTTCACACT[G/T]ACTTGAAGGTGGGGA	84182
rs138023075	in-del	-/C	0.00601687	0.0545182	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859245	AGCTCATTTTTCTCT[-/C]CCCCCTCCCAGTTTG	84182
rs138066399	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30890931	AATGTCAGGAATCCT[C/T]GACTTTCTGGATGTA	84182
rs138072445	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30835344	TGAGACTTATTCACT[A/G]TCATGAGAACGGCAC	84182
rs138109310	snp	C/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30784626	CGGCTGCTCCCCTGA[C/G]CACATTCTGCCTTAG	84182
rs138112353	in-del	-/CG			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30880309	CCCCCGCACCCCCCC[-/CG]CCACCCCCGACTGCG	84182
rs138114370	snp	A/C	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30849394	AAATTTGCAGAATCC[A/C]AGAGAAGCCTAGAAG	84182
rs138119447	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30780218	TGACCCAGGCAGCAG[A/G]TGCTCTGCAATCCTC	84182
rs138127356	in-del	-/G/GG			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30794727	GTGGGGGTTGTGGCT[-/G/GG]GTTTGGGGCCACCTG	84182
rs138164091	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872532	TCTGGACAGCTTTAT[A/G]TGCACTGATGTATGT	84182
rs138187392	in-del	-/AT	0.021333	0.101051	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30806503	AACAGATGGATATAT[-/AT]TCCTGAATAGATGGG	84182
rs138234355	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30876327	GGATTAAGGGCCCAC[C/T]GTACTCCAGTATGAC	84182
rs138243647	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30879670	CGTTTTGACTTAAAC[A/G]TTACTTCCTAAAAGG	84182
rs138247237	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30775373	CATTTACCAGTTTAC[G/T]ATAAAGGACACAATT	84182
rs138259591	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30867132	AGCGATTTACCAAAG[A/G]TCACGCAGTGCAGGT	84182
rs138263661	snp	A/G	0.00557542	0.0525036	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840301	GGGGCAGAAGAGAGC[A/G]CAGAGCTCATGTAAC	84182
rs138277668	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30846029	AACGGCCCTCAGAGG[C/G]GGGTGCGGATCTGAG	84182
rs138307544	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30857802	CATCCTCTTGGCACA[A/G]AAATTTCACCAATAC	84182
rs138319795	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30831170	CTCTTACCTGGGAAA[C/T]CCAATGGGTATTTCA	84182
rs138371071	snp	A/C/G	0.00107496	0.0231618	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836614	CATGTTCTGTTCTCC[A/C/G]TGAGTCATAACGAAG	84182
rs138386603	snp	A/G	0.00676609	0.0577691	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30803165	CTATACTTGGACATG[A/G]TCTGTTTCTCAGACC	84182
rs138423272	snp	C/T	0.000113488	0.00753201	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859042	CTTTGGTGGCCCCTG[C/T]ATCACCCTCGCTCTG	84182
rs138424277	in-del	-/A	0.113334	0.209338	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882728	AGTATTGTGGTAGCT[-/A]AAGTGGGACACGGGT	84182
rs138466164	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30806651	CCCTTGGGCATGTCT[C/T]TCCCCTGGGGTCAGG	84182
rs138557731	snp	A/G	0.00478085	0.0486577	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30823876	ATCTTGTTTGAACTG[A/G]TTTGTAGGAATGCTC	84182
rs138591836	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859601	CCTGGAACTGCAGTG[C/T]ATGCACACTTGAGCA	84182
rs138621153	snp	C/G	0.00795532	0.062565	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30891497	AGTAAAGCCCAGAAC[C/G]CTTACAAGTTCCTGC	84182
rs138639794	snp	C/T	0.000399281	0.0141238	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785889	TAGACAAGCTTCACT[C/T]GGAGCCTTCCTTGGA	84182
rs138653807	snp	C/T	0.00478085	0.0486577	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850267	GCACCTCCTTTGGCC[C/T]TCAGCTGTGGAGACC	84182
rs138672176	snp	A/G	0.0221141	0.102801	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30885312	ATCACCTGAGGTCGG[A/G]AGTTTGAGACCAGCC	84182
rs138673352	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30817806	TATGTCTGTCCATGT[C/G]TGAACAACTCTCTCA	84182
rs138710331	snp	C/T	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30794353	AAGCGTGGGAAAGTG[C/T]AGTGAGATGGCATCA	84182
rs138740263	snp	C/T	0.00211243	0.0324307	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853380	ACTCATCCTGAGTGT[C/T]TGTGTCTTCTCAGCT	84182
rs138745528	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30789889	GAGGATATTTGGATA[G/T]TTCAATTGACTCCTC	84182
rs138807465	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30845502	GAAATTCTAGGATTT[C/G]AGACATGATCCAGCT	84182
rs138867029	in-del	-/CCTTTCTTAAG	0.0912534	0.193131	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30800992	CCAGGCCCTACCAGA[-/CCTTTCTTAAG]CAGTCCAGGGGGAGA	84182
rs138870166	snp	C/G/T	0.00478085	0.0486577	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30810234	AAAGTTGAGGCATGT[C/G/T]GAAGAGTTGTCTGCG	84182
rs138887205	snp	A/C	0.0221141	0.102801	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30880933	CTTCAGAGCACAGCC[A/C]CTCTGTCAGAGACAT	84182
rs138909898	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872085	CTTCTGGGTGGGAGC[C/T]TCCTCCGTGGAGGGC	84182
rs138922772	snp	C/G	0.00636936	0.0560724	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30863221	CAATTGAAAACATGT[C/G]CTGGTAGCAAAAAGA	84182
rs138933963	snp	C/T	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30800018	CATCCTGGAGTGGGG[C/T]GGGCAGTGTGCAACC	84182
rs138948040	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30874749	CTACTGAAGTACCTT[C/T]CTCGGCTTTCCCTGC	84182
rs138974650	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30770339	GAAGTCCTAATGCCT[C/G]GTATTCCAGAATGTG	84182
rs138976557	snp	C/G	0.00517822	0.0506191	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840941	GCATGTGTGTTCCCT[C/G]ATATTTCCTGTCTTC	84182
rs138996699	snp	A/G	0.00438332	0.0466095	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30814927	GGGAATGCCTTATAA[A/G]TTTGAAAGGAAAATA	84182
rs139005271	snp	G/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782426	AAGAAGTTTGGCCAG[G/T]TGCAGTGGCTCACGC	84182
rs139012586	snp	C/G	0.0185938	0.0946107	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30880249	TGTGCTACATGTTCC[C/G]CCACCAGGACAAAGT	84182
rs139114308	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30883116	CTGATTCAAAGAGGT[A/G]TGGTGATTGGAAAGA	84182
rs139115748	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30775890	GGAATAAATGGCATC[C/T]CTGTCCTTCTAGTTG	84182
rs139116019	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30817170	TCCCATCCTCTCCCT[A/G]GAGCTTGGTTTCCTT	84182
rs139116981	snp	A/G	0.00358779	0.0422022	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30847139	GGCAACGGTTTTACC[A/G]GAACCTGTGAACCAG	84182
rs139134362	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30841188	CTTTCGACTGCGTCC[A/G]GGCCTCCCTTCCCTC	84182
rs139189101	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30812123	TTAAAAAGTGTTGTC[G/T]TACAAACAAACCCCA	84182
rs139203164	snp	A/G	0.00597247	0.0543191	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30815827	GAAGGGCAGGGAGGT[A/G]TGAACTGGGAGGGCC	84182
rs139238183	in-del	-/C	0.0123036	0.0774623	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30775294	TGAGGGTTCCCACAA[-/C]CCCCTCCACAGTTTT	84182
rs139281905	snp	A/G	0.00438332	0.0466095	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30860359	GGCTGCCTGCTGCTT[A/G]CTGCTTCTGACCTTA	84182
rs139282839	in-del	-/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30885702	CAGGTAAGGGCAGTG[-/C]CCCACCCCCCCCCCA	84182
rs139311248	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30826310	ACGTATCTGTGTAAT[A/G]TGTTTCTTCTGGGCA	84182
rs139413978	snp	A/G	0.00914312	0.0669923	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30820440	CATTCACAGTGTTGT[A/G]TAACCACCACCTCTG	84182
rs139429114	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30887957	ACGGGAACGGAAACT[C/T]TCACACAGGCCTATT	84182
rs139519844	in-del	-/AGA	0.00358779	0.0422022	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30826407	TGTTCTTTGGAGCTG[-/AGA]AGAAGCTGATGTTCC	84182
rs139539237	snp	C/T	0.0119091	0.0762411	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30846964	TCACCTCCTGCTGTG[C/T]GGCCTGGTTCCTAAC	84182
rs139541808	snp	C/T	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30831529	GAGACATTCTGGAGG[C/T]AGAGTGATCCAGAGG	84182
rs139580851	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30834987	AGTTTCAAACTTTCC[C/T]ACATTTTCCTGTCTT	84182
rs139596467	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30864671	TGGGCTGCACCATCA[C/T]ATATATATGGACATG	84182
rs139623033	snp	A/G	0.00517822	0.0506191	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30800279	TGGATGCCCTGGTGA[A/G]ATGGGCCAAGCAGGG	84182
rs139637351	snp	A/T	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30805054	AGAGGGATAGAAAGT[A/T]CTCTTGTGTTTTGGG	84182
rs139681722	in-del	-/AGT	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785380	TTCTCCACGCCTCTC[-/AGT]GGTGTGCGGCAAGGC	84182
rs139683865	snp	A/G	0.00398564	0.0444627	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30869316	GAGGAGGAGAAGGAT[A/G]GGACAAGCCTCCACA	84182
rs139717696	snp	C/G	0.0225045	0.103662	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872804	AGCACAGTTGCTTGT[C/G]ATCAGTCCTCTCAGT	84182
rs139759386	snp	C/G	0.00398564	0.0444627	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30804302	AAAGCCATGGGATTT[C/G]TTTCATTTCCTGTTG	84182
rs139767948	snp	C/T	0.00914312	0.0669923	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30811155	CTGCTGTTCATTCAG[C/T]GGAAAAGGGATGGAC	84182
rs139782481	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791679	TCTTAGTCTCCTTGG[C/T]CTCTCAGAACAAGCC	84182
rs139798914	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30816156	AGCTTCCAGAGGGAG[C/T]ATCCATTGAATACCA	84182
rs139822334	snp	C/G	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30883653	TGGGCCCCTGGGCTG[C/G]TGGTGCGGTAGCTGT	84182
rs139842076	snp	A/C	0.00318978	0.0398085	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30886778	TTGCTGTGACGCAAA[A/C]CTCGGCCTGAGAGAG	84182
rs139892423	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30781707	CATGCCTCTATTCCT[A/G]TCACATTTTATTCTA	84182
rs139937494	in-del	-/T	0.0325976	0.123435	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30776137	TCCTGCCTCCTACAG[-/T]TTTATTTTCAACCTA	84182
rs140012836	snp	A/C	0.000399281	0.0141238	downstream-variant-500B	FAM188B, INMT-FAM188B	GRCh38.p7	7:30892797	TCATGAAGGGGATAT[A/C]GTAGTCTGAGCCTTG	84182
rs140028122	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30851341	TGTAATCGCTCTGTT[C/T]ACTCATCTGGAAAAT	84182
rs140034140	snp	A/G	0.00993419	0.0697739	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30864244	CTGGGCAGGACCCAC[A/G]CCATGTCACTCTGTG	84182
rs140053367	snp	C/G	0.0107246	0.0724382	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30867332	GTGGTTGAGATGGCA[C/G]GAATCATGACCTCTT	84182
rs140073449	snp	C/G	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30829194	CTTAAGTGCCCTGGT[C/G]TGCATCTTCACTTCT	84182
rs140100692	snp	G/T	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30831281	AAAACCCTTGCACTC[G/T]TTCCTTTTTCAGCAC	84182
rs140103996	snp	A/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30851930	GGTGAGAGTCAGACT[A/T]CCTACTGCCAGGGCT	84182
rs140107267	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30873712	TCTTCACCATCTCAA[A/G]AAGGCTTCCTGCTAT	84182
rs140144900	snp	A/G	0.00716266	0.059414	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30855715	ACCAAGACAGGGACT[A/G]TGGAAGGGGTTCAGA	84182
rs140145973	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30835999	GGGATGGTAGAGTTA[C/G]TAGGAGTCACTCTCT	84182
rs140175577	snp	A/G	0.000220326	0.0104935	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791184	CTTTTCACAGACACT[A/G]TCTGAGACGGTCCTC	84182
rs140199320	in-del	-/AC			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30861005	TGGCCACACACAGAG[-/AC]ACACACACACAGACA	84182
rs140242076	snp	C/T	0.0023933	0.0345097	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30794829	CTGGCCCTGACTGGG[C/T]AGTCCTCTAACCCTC	84182
rs140248723	snp	C/G	0.00557542	0.0525036	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30809073	AGAAAAAAAAACAGT[C/G]TACCCTATTCCTTTA	84182
rs140260828	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30790848	TTGCCACAGGTGACA[C/G]AGTTGGTAGGTGGTG	84182
rs140355783	snp	A/G	0.00478085	0.0486577	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30832428	TGGAATTAATCACAC[A/G]TCTCTTTTCCTCCAG	84182
rs140397627	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30797632	CTGGAAGCTGCTGAA[G/T]GCATTGGCTTTTACT	84182
rs140401060	snp	C/G	0.00358779	0.0422022	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30858019	TTTTCATTGTCTGTT[C/G]CAGGAGAAACAAGTT	84182
rs140401719	snp	C/T	0.0023933	0.0345097	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30822589	AATCCAGGATCCATT[C/T]GAGGTTTGCCCATTG	84182
rs140406823	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30890322	TTGTGTCTAGACTAG[A/G]ATGAACGTGACATCC	84182
rs140435223	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30873083	TCCTGGCTCACTTGC[A/G]CCCAGCTCTGGAAAC	84182
rs140440317	snp	A/G	0.00398564	0.0444627	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30860614	GATGCCAGTCTCAGC[A/G]CCCCCATCCATGCGG	84182
rs140462837	snp	A/G	0.00636936	0.0560724	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30817278	ACCTAGAGGAGCTTG[A/G]CTGAGGAGCTACAGG	84182
rs140466553	in-del	-/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30888550	TTCCATTTCATCCCT[-/C]CCCTTTCTGTGCCTG	84182
rs140527943	snp	A/G	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30877234	GGGCCAAGAGAGGCA[A/G]CCTTGGCTAGGCTCA	84182
rs140547192	in-del	-/TTTTGTTTATA	0.48178	0.0936921	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30793156	TATATATTGTTTATT[-/TTTTGTTTATA]TAATTGTTTATATAT	84182
rs140556930	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30879271	CTCCTAAGCAGAGGA[A/G]GTTAGGACACAGATC	84182
rs140599963	snp	A/G	0.0023933	0.0345097	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30775138	CACCAATTGGGTGTC[A/G]TACAATTCAAATCAG	84182
rs140676813	snp	A/G	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30772309	GCTAGGGCGATGGGT[A/G]CTTGTCTTGTATGAA	84182
rs140716551	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839689	CAGGATTTTGCAGAT[A/G]GAGCTGGAGAAAGGG	84182
rs140727793	snp	C/G	0.000170488	0.00923121	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839185	AACCAGTAAAACTCT[C/G]TCTTCTTTTTATAGG	84182
rs140736531	snp	A/G	0.00358779	0.0422022	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30843460	TAGTGCTCCTTCAGA[A/G]TTGCTTTTGAACTTC	84182
rs140771879	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30774459	AGCACATGTTGTGCT[C/T]CTGCAGAATCCCATC	84182
rs140774399	snp	C/T	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30805161	CAGCAGGGCCCCTGC[C/T]GGGAAGGCAAGTGGG	84182
rs140790848	snp	A/G	0.00358779	0.0422022	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30858296	ACAGCTAACACAGGT[A/G]CCAGGCCCTGTTTGA	84182
rs140855163	snp	C/T	0.0023933	0.0345097	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30856263	GCCTTTCAATGCAGG[C/T]GTGTTGCCCTGTGGC	84182
rs140878240	snp	A/G	0.00438332	0.0466095	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30801179	GAGGATGTGGCATTT[A/G]CGGTTCATTGACTGT	84182
rs140899016	snp	C/T	0.00517822	0.0506191	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853204	CGACTCCAGCGGTAC[C/T]GGCCAGCCTTTCACT	84182
rs140946970	snp	C/T	0.0023933	0.0345097	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30821218	AATTGTTTTTATTGT[C/T]GGTTCTCATTTAGGT	84182
rs140952635	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30784274	CAGTTACCCAAGCCA[A/G]AAATTTGGGTGTTCT	84182
rs140974842	snp	A/G	0.0263992	0.111815	utr-variant-3-prime, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30892202	CCCAGTGTGTTGCTG[A/G]GTCCCCTCCCAGCTG	84182
rs141005246	snp	A/G	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30884547	CCTTCCTGCAGGTGG[A/G]CCTGTTGAGCAGGGC	84182
rs141010224	snp	C/T	0.00398564	0.0444627	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30825766	AGAGAATACTGCAGT[C/T]GTTTCTTCTTCCTTG	84182
rs141015205	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30891361	GTTATTCAGTTGTCT[C/T]TAACCCTGGACCACA	84182
rs141024371	snp	C/T	0.00358779	0.0422022	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30787094	GTCCTCTCCCTGCCC[C/T]TGGCTCTATCTTATG	84182
rs141052324	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30844838	AGCATCACTTTCTCC[A/G]TTTGTGAACTAGGAA	84182
rs141057795	snp	C/G	0.00636936	0.0560724	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30779060	AAAGCAAATGGAACT[C/G]TGTTTTCTTGGGCGG	84182
rs141112932	snp	A/G	0.00636936	0.0560724	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30826744	TTGCTGTGTAACCCT[A/G]GGAAAATTACTAAAC	84182
rs141125214	snp	A/C	0.0166325	0.0896639	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30789060	TTGTGCACAAAGTCA[A/C]CACAGTGGAAAAAGG	84182
rs141127097	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30829781	AAACCCTTTTTGTGC[A/G]CCACTGCACTTTAAG	84182
rs141135035	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30855566	GGGTGATTGCTCAAA[G/T]GACCACAGATCCTGA	84182
rs141141905	snp	G/T	0.0260105	0.111035	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30833865	CAGTCAAATCTTAAA[G/T]CTCCAAAGTGATCTC	84182
rs141173304	snp	A/C	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30819594	AAATTTTCTATTATG[A/C]TCACGGATTGAAGAG	84182
rs141241436	snp	C/G	0.0023933	0.0345097	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30802182	TCCAGCAGTTCCTGG[C/G]TACCAGAATCCCATA	84182
rs141259132	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30865314	GGAACTTCCTCAATA[A/C]ACTCCAGCCGAACTT	84182
rs141259278	snp	C/T	0.00478085	0.0486577	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30881740	ATGCAGGCTGTCCAA[C/T]GGTAAGCAAGCTCTA	84182
rs141270012	in-del	-/CAGTT			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30856220	TCTAGACCCTGATGG[-/CAGTT]CAGTTTTCAGGCCAG	84182
rs141284567	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30815608	GAACTGCATACCCCA[A/G]GCCAGAGTGGTTACT	84182
rs141296837	snp	C/T	0.0123036	0.0774623	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30776672	GAGTGAGCATGTGGA[C/T]GATGCTGAACAAATA	84182
rs141419487	snp	A/G	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840655	CTGTTGCAGAAGGCA[A/G]GGCCCCTTTACTCTA	84182
rs141422796	snp	C/G	0.0103295	0.0711199	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30874263	CTCAGTAGGCCCTTA[C/G]AGGCCACCCTTCATC	84182
rs141424907	snp	C/T	0.0287284	0.116357	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30809903	AATGTTTAGGCCGGG[C/T]GCAGTGGCTCACGTC	84182
rs141436874	snp	C/T	0.00716266	0.059414	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30812586	TAGCCCAAAACACGC[C/T]GAGGGAGCAGCTGAT	84182
rs141438703	snp	C/T	0.00199481	0.0315187	upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30770107	AACATGGTGAAACCC[C/T]GTCTCTACTAAAAGT	84182
rs141443603	snp	C/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30807797	CCCGCAGTCACGTAC[C/G]CCCTGCTTGCTCAGT	84182
rs141459059	snp	A/G	0.00398564	0.0444627	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30878426	TGCCATAAGTAACTG[A/G]TCCGGCCTGGCTGTG	84182
rs141537215	in-del	-/AA			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30858648	AAATGTTGATGTTTT[-/AA]AAAAATATATATATA	84182
rs141550013	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30802834	CCCAACCAACCAACC[A/G]TCCCAACCGACCAAC	84182
rs141553719	snp	C/T	0.00358779	0.0422022	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30884729	CTCCAGAAATTATTC[C/T]ACTGCATGACTCACC	84182
rs141570642	snp	A/G	0.00358779	0.0422022	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30866539	AAGTCCTTGCCACCT[A/G]GAGAGGCAAGACCAG	84182
rs141581205	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30886811	TCCTGTTACCTTTGC[C/T]TGTGTCAGGAATGTG	84182
rs141610593	snp	G/T			utr-variant-3-prime, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30892147	ATCCAGAGCCTCCCT[G/T]CCCCTTCCATGAAGG	84182
rs141620195	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30891574	CAGCCATATCTAGGA[C/T]TGCACAGGTGCCTCT	84182
rs141640116	snp	C/G/T	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30889552	GTTTGTCTCCAAATA[C/G/T]GGCACCAGTGTCTCT	84182
rs141642052	snp	C/T	0.00358779	0.0422022	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30845827	GTTTTTTCTGCAGGA[C/T]TGTCTGGCTTCATTA	84182
rs141642244	snp	C/T	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30779728	CAGGTAGGGATGAGG[C/T]TAGAACCAGGTGTTT	84182
rs141654682	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30783602	ATGAATTAATAGATT[C/T]TGGGGATCAGGATGT	84182
rs141679971	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30848705	GGTAACTATTTCCTC[C/T]AAGGAACATGATGGG	84182
rs141690752	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30794131	CACAACTCTACACAG[C/T]GCTCTTGATTTGAAA	84182
rs141715166	snp	A/C/G	6.66837e-05	0.00577386	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850506	CTCGTCCTGGCCCTC[A/C/G]CAGACATTGTGTGGC	84182
rs141737893	snp	A/G	0.00398564	0.0444627	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30846730	TGGCACCAGGGACTG[A/G]TTTTGTGGAAGACAA	84182
rs141757181	snp	A/G	0.00358779	0.0422022	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30854039	GCTGGGCGGGACGTG[A/G]CCAGGGCCAGACAGC	84182
rs141781579	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30790003	AGAGGCGAATTAAGA[A/G]TGACCTCTGCCATCA	84182
rs141841701	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30876098	GCTGGAAGTCCAAGA[C/T]CAAGGTGTCAGAAAG	84182
rs141888334	snp	A/G	0.000596253	0.017256	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836701	AGAGGTCATCCTGTC[A/G]CCAGTCCCATCAGTG	84182
rs141957722	snp	G/T	0.00993419	0.0697739	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30867598	CTTTAGAGCCCAAGT[G/T]CTCTTGGTTGTACCA	84182
rs142006177	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30834556	GACGTTTTCCCCATT[A/G]TCTTGTGGATTAACA	84182
rs142013680	snp	A/G	0.00478085	0.0486577	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30830399	TTAGTGTATTCTCAT[A/G]CTGCTAATAAAGACA	84182
rs142018076	snp	G/T	0.0154538	0.0865337	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30799633	GCATCTGCATCATCT[G/T]GGAACTTTTTAGAAA	84182
rs142062552	snp	A/G	0.00318978	0.0398085	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30869620	CTTTGGTGTCCCTCT[A/G]TGTGTCCAGATTTCC	84182
rs142102103	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30873151	GGTTTGTCCAGGGCA[C/T]CCACAGAGGGACCGT	84182
rs142117817	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30834825	GCAAATCTCTAGGGC[A/G]GAGGCAAAATGCTGC	84182
rs142154879	snp	C/T	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836485	TGGTTGCTTTCCTTC[C/T]GCTAAGGGTCTGGGA	84182
rs142209536	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30868951	GCCAGGGCCAAGCCT[A/G]TTCTGTGAGTTTTCA	84182
rs142255354	in-del	-/CTG	0.354235	0.227234	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30786733	ATAGTTTCATTTATT[-/CTG]CTTTTATTTTTTTCT	84182
rs142261392	snp	A/C	0	0	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30800898	GACAGTAGATGGCAG[A/C]AGATCTTCATCAATC	84182
rs142347783	in-del	-/T	0.0325976	0.123435	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30862887	GAAAACAAAATCTGA[-/T]TTTTTTTTACCCAAA	84182
rs142349217	snp	C/T	0.00557542	0.0525036	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30848996	TCTCCTTTAAAGCCA[C/T]GAGGGAGGTGCAGTG	84182
rs142363589	snp	A/T	0.00676609	0.0577691	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30795911	TTGAGGACCTTTGTG[A/T]TTACCTTGGACCCAC	84182
rs142381474	snp	A/G	0.00953873	0.0683987	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30814555	TATGCTGCTTTCTAC[A/G]CAGGACTTTCGTGAG	84182
rs142386284	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30860266	CTGGTTGGGTCTGGT[C/T]GGCGCCCTCCCTGTT	84182
rs142428339	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30848411	AGGGGAAGGGTGGGC[A/G]TGAGGTACTCAGGAT	84182
rs142455059	in-del	-/AG	0.0722614	0.17581	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859620	CACACTTGAGCACTC[-/AG]GGGGATGCCCCTGGC	84182
rs142479913	snp	C/G	0.0166325	0.0896639	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30818388	GGTAACCTCATTAAT[C/G]ATCATTATCTCAACT	84182
rs142526753	snp	C/T	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30886749	CCATCCCAGACCCCA[C/T]GTGTCTCTGCGCTTT	84182
rs142529989	snp	C/T	0.00835141	0.0640778	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30786333	GAGAGCATCTTTAGG[C/T]TGAGTGTGGTGGCTT	84182
rs142542679	snp	G/T	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30774299	TGCACCATTCACTCT[G/T]CTCTCTTTAGTGTTC	84182
rs142579979	in-del	-/CTGT	0.384401	0.210799	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30822620	TCTTGGTTGACGTGC[-/CTGT]CTATTTTATTTATTT	84182
rs142599188	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30781287	AATTTAAATCCTTGC[C/T]GTTGTGGTGTAGTAA	84182
rs142599519	snp	A/G	0.00716266	0.059414	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30823035	TTGTTGGTTTGTTTC[A/G]TTATTAGGTTTACAT	84182
rs142663668	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785166	AAATTTCCAGATGCT[C/T]TGGTAGGTCAGAAGC	84182
rs142674615	snp	C/T	0.0134861	0.0810011	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30835254	AGGAGGAGCAAGTCA[C/T]ATCTTATGTGGATGG	84182
rs142753822	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30857131	TTGAAAAGTAAATGA[G/T]GTCCTCAGGGCTCTG	84182
rs142763583	snp	A/G	0.00358779	0.0422022	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30831940	TAGCATTCTCAAACC[A/G]CTGACATTTACAGAT	84182
rs142874659	snp	C/T	0.00636936	0.0560724	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30803503	TGCTAATTGAGATGC[C/T]GTAGGAGCTTAGAGG	84182
rs142881651	snp	A/G	0.0023933	0.0345097	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840942	CATGTGTGTTCCCTG[A/G]TATTTCCTGTCTTCT	84182
rs142912491	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828790	GGCCCAAGGGGTCCT[C/T]GTTGGCTCTGTCTGG	84182
rs142926471	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30867203	CTACTCCCTCTTGGC[C/T]ATCCTGGGAAAACAG	84182
rs142944427	snp	C/T	0.00127626	0.025229	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791390	CATCTGCCCAGCAAA[C/T]GGCTGCCCCCATGGG	84182
rs142944441	snp	C/T	0.00597247	0.0543191	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30884325	GTCCATCCACCTGCC[C/T]GCCCCCTGAGCCAGG	84182
rs142967420	snp	A/C	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30880696	GGGTTTAGGCACGTC[A/C]AGCCACGTCCTGTAA	84182
rs143021048	snp	A/C	0.00318978	0.0398085	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30802663	TTAAAAGTGGTAAGT[A/C]TTTCATATAATTGAA	84182
rs143034466	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30776094	TTTGTGAATTGTTCA[A/G]TAGCCTCCTAAATGG	84182
rs143108822	snp	C/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30862143	CCTCCAGTGCTCCCT[C/G]CTGACTGTTGCATGC	84182
rs143126494	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30883842	CTCTGGAGAGAAGTC[C/G]CCTGGGTTCCAGCCC	84182
rs143150521	snp	C/T	0.00517822	0.0506191	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850160	TCACACACTTCTGGG[C/T]CCCACCAAGCCTGCA	84182
rs143210552	snp	C/T	0.00597247	0.0543191	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778177	TTCCAAATGTAGGGC[C/T]AAACCCAGGACTCCT	84182
rs143222855	snp	A/T	0.000232084	0.0107698	stop-gained, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782100	CTCTCAGTTCCAAAG[A/T]AAAATAACAAAGTGC	84182
rs143254469	snp	C/G	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30846983	CTGGTTCCTAACAGG[C/G]CACAGACCAGTGCCA	84182
rs143259818	snp	A/G	0.00716266	0.059414	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852434	AGGGTGGGGACAGAC[A/G]TGGGGTGGCTTTGGG	84182
rs143273914	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30827745	GATTTGGTACTGTGC[A/G]TCCTCTAGCTCTTCC	84182
rs143301136	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840426	GACAATTAACACCCT[A/C]AACCTGTAGACACAG	84182
rs143331869	in-del	-/A			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30809799	AAAAAAAAAAGGGGG[-/A]AAAAAAAAGGGGGGC	84182
rs143336412	snp	A/G	0.00398564	0.0444627	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30790904	CTGCTGCATGAACCT[A/G]CTCTCTGTAAGGGCT	84182
rs143390461	snp	A/G	0.0463947	0.145069	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30862983	GAGGTGGGAGGGAGA[A/G]GCCCCTGCTGCCCCC	84182
rs143394417	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30825449	TTCCCACCATCTCAG[C/T]GGGCTCATGGCCACC	84182
rs143396851	in-del	-/TCC	0.0663309	0.169604	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30878771	GTTCTGAAAGCTCCA[-/TCC]TCCTCCCATCCTCCC	84182
rs143458880	snp	A/G	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30827383	GAGCAGGCGGAGGTG[A/G]GAGAAGTGTGGCTGG	84182
rs143545235	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30830195	ACTCTTGTCAGCAAT[A/T]ACCTGCCAGCGCATA	84182
rs143551449	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30793991	GCACAGAGAATCCAA[G/T]GAACCTGACAAGGTT	84182
rs143557074	snp	A/G	0.00318978	0.0398085	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30877933	GATCCACCCACCTCA[A/G]CCTTACAAAGTGCTA	84182
rs143567874	snp	C/T	0.00517822	0.0506191	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30886092	GGATACACGTGACAT[C/T]GTGGCATGAGCTCAG	84182
rs143641582	snp	A/G	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30829390	GACCAAGGACTGGCC[A/G]TGAGAGGATGAGGCT	84182
rs143657574	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30822281	TTCCCAGATTCAAGG[A/G]ATCCTCCCACAGTCC	84182
rs143683014	snp	C/T	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30831310	ACTTACTAGGTTATG[C/T]TGTAATTTTTCAGGG	84182
rs143686395	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30811190	CACACCCAAGTCAAC[A/G]TGTTAACAGTTAACA	84182
rs143696034	snp	C/T	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30810592	ATTAAAGTAAAAACA[C/T]GACCGGTTTTTCTTA	84182
rs143719637	snp	C/T	0.0166853	0.0898011	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875623	CAGTGATATTGGCTT[C/T]TTATCTCTCTTTGAG	84182
rs143750152	snp	A/C	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30773448	GACTTCAAGTCTCTC[A/C]ATTACTTGGCTCTGG	84182
rs143756843	snp	C/T			upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30770725	CCAGGTGACTAAGTT[C/T]GGGGAAAATGTACTG	84182
rs143797561	snp	C/T	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778978	CTTAGTCTTGAGTCT[C/T]CTGTGACATATAATT	84182
rs143830029	snp	C/G	0.00716266	0.059414	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30870572	ATCTTCTCATGTGGA[C/G]CATAAACCTTCCGTG	84182
rs143872266	snp	A/G	0.0566069	0.158427	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30810768	ATAAAGGTGAAATTT[A/G]GCTTATCTGGTATAA	84182
rs143893207	snp	G/T	0.00993419	0.0697739	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30855425	GGCATCCGTGTGTGG[G/T]ATCTGGCCAGGGTGG	84182
rs143907640	in-del	-/TGTT	0.0111196	0.0737302	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30862863	TGCTTTTTTAAACTA[-/TGTT]TGTAATGAAAACAAA	84182
rs143924949	snp	A/T	0.00597247	0.0543191	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30878869	ACATGTGCCTCCCCC[A/T]GAAGTTGTTTCTCAA	84182
rs143958818	snp	C/T	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30841718	GAATTATCACAAAAC[C/T]GCACACCCATGAACA	84182
rs143959227	in-del	-/C	0.0150606	0.0854603	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30813346	GTTAAAGTGTTCAAT[-/C]CCCAGGTCCTGAATT	84182
rs143963902	in-del	-/TGAAT			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839657	GGCCTTCTTAGGCTG[-/TGAAT]ATCATTGAGAGATTC	84182
rs143969720	snp	C/G	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30847952	TGCCTGGGCTGTTCT[C/G]AAACTCCTGGCCTCA	84182
rs144020635	snp	G/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30815950	CCAGCATGGGATAGA[G/T]TAAAATAAACCAAGA	84182
rs144137725	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30860885	GGGAATGCTGCCCTG[C/G]TGGACCTTCACAGCC	84182
rs144162786	in-del	-/C	0.154993	0.231244	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30818138	TTATTTTTAAAGAAA[-/C]CATATATGGATATTT	84182
rs144171330	snp	A/C	0.0158469	0.0875917	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30815236	TTCCCTTTTGTCATG[A/C]CAAGGATGACTTTAG	84182
rs144232998	snp	C/T	0.0197687	0.0974348	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30835152	GCTGATAAAGATACT[C/T]CTGAGACTGGGCAAT	84182
rs144235389	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30796472	TGATATAGTCCATGC[A/G]ATTGAAGTCTAATTT	84182
rs144247731	snp	A/C	0.00438332	0.0466095	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30800548	GGGTGCACTGGGATG[A/C]CCTGTGTAATTGGGT	84182
rs144337538	snp	G/T	0.00716266	0.059414	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30831231	AGTTTCCCTGAGCAT[G/T]TATAGCAGAATTAAT	84182
rs144344081	snp	A/C	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30795454	GGAGCCGTGGGATCC[A/C]GGGGTACCAAGATAT	84182
rs144373832	snp	C/T	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30835605	GTGCTGTGGCTGGGT[C/T]GCCCTGGGGAGAAAG	84182
rs144400951	in-del	-/AG	0.0174175	0.0916809	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872493	CATGGAGACCCAGAA[-/AG]AGAGCTCAGTTTAGC	84182
rs144436645	in-del	-/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30885707	TAAGGGCAGTGCCCA[-/C]CCCCCCCCCAACCCT	84182
rs144449035	snp	A/G	0.00953873	0.0683987	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30824374	AGCACTCATGACTCA[A/G]TCATCTCCTGAATGC	84182
rs144475488	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30804967	CCCAGGGGATGTGTG[A/G]GTGGTGGGAAGAGGG	84182
rs144499524	snp	A/G	0.0228947	0.104514	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30877412	AATTCAGGCCCTACA[A/G]CCATCTCCCCTCCTC	84182
rs144509099	snp	A/G	0.0020018	0.0315736	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785913	CCTTGGATGTGAAGA[A/G]GATGGGAGAGAATTC	84182
rs144512461	snp	A/G/T	0.0126979	0.078662	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30812115	TCCTGGTTTTAAAAA[A/G/T]TGTTGTCGTACAAAC	84182
rs144573901	snp	C/T	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839541	GATGTTAAAATTGAA[C/T]ATGGATTTAAGGAGC	84182
rs144587387	snp	C/T	0.00398564	0.0444627	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30780288	TTTAGGAGAATTTTG[C/T]GCAGAGAGTGAGACA	84182
rs144591416	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30774492	GACCCCCAAACCCTA[A/G]CTACTGGTTTATTAT	84182
rs144621104	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872663	GGGGACCCTGGGTCC[A/G]GCTGGGGAGATGATG	84182
rs144629523	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30846450	CTTCACCTGTGAGGA[A/G]TTCGACTCTTAAAGA	84182
rs144675965	snp	A/G	0.00438332	0.0466095	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30868170	ACAAGCTGTGCCTGA[A/G]CCAGCAATGGTGGGG	84182
rs144677181	snp	A/G	0.00795532	0.062565	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30804844	GGACTGTTGAGAGCT[A/G]GCATTAGCAAGGACA	84182
rs144766311	in-del	-/TC			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30870042	AGCCACTCCTTGGCA[-/TC]TCTCTCTCTCTCGAA	84182
rs144769522	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30823537	TTTAATGTATCATCT[A/G]TCACCATTGTTATAT	84182
rs144777465	snp	C/G	0.0107246	0.0724382	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30891390	CAATTTAGTTATACT[C/G]CGTGCTTCTTCAGGT	84182
rs144782601	snp	C/G	0.00716266	0.059414	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30889007	TACTTCAGTCTTTCT[C/G]AGTGGGGAGGGTAAA	84182
rs144783758	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30826760	GGAAAATTACTAAAC[A/G]TCTTTGAGGCTCAGT	84182
rs144784246	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30863468	GTGACTTGATTGTGT[A/C]CATGTGCATGTGATT	84182
rs144794574	snp	A/C	0.00358779	0.0422022	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828549	GGGAGTATTCAAGGC[A/C]CACAGAGGCAAGGCC	84182
rs144806274	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30821457	TTGTCATTGCTATTG[A/G]GAAGTCTGCTGTAAC	84182
rs144869544	snp	A/G	0.00716266	0.059414	downstream-variant-500B	FAM188B, INMT-FAM188B	GRCh38.p7	7:30892421	ATTTGTTCTACAGCT[A/G]CAAAGAGCGTGATGT	84182
rs144871553	snp	C/T	0.00358779	0.0422022	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30825848	ACCACAAAGTGGCTT[C/T]AAACAACATGAATTT	84182
rs144871673	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30783166	CTGGAGGTTCTGAGG[A/G]GAAAATCCATTTTCT	84182
rs144885784	snp	A/T	0.0517044	0.152246	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30787638	AGCTGGCACCAGTGG[A/T]TGGAGGTTGGTATGG	84182
rs144973182	snp	C/G/T	0.00358779	0.0422022	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30826715	ATTCCTGTGCTGCCA[C/G/T]GGGATAGGGTTACTT	84182
rs144974743	snp	A/G	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30808498	TTTGTTTTGTGTTGT[A/G]CATGTGGTGTGAGCG	84182
rs145013066	snp	C/T	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30798030	ACCTGTCTCTCTCCT[C/T]GAGACTGCTGAAGTG	84182
rs145083187	snp	C/G	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872002	GCCCTGGTGCGGCTG[C/G]AGTGGAGGCCATTGC	84182
rs145129382	snp	A/G	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30874346	GAGGGAAGTCACATG[A/G]GACAGAGAGAACCAG	84182
rs145176048	snp	A/G/T	0.00199529	0.0315338	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836370	ACTCTATGTCCATGC[A/G/T]TGGAACTTTCTAGTG	84182
rs145193963	snp	A/G	0.00914312	0.0669923	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30869593	CTTCATCTTTTCCTT[A/G]TGAGTGTGCATCTTT	84182
rs145206659	snp	A/T	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30826656	ATAAGGAAGCAGTAA[A/T]TGTAGTTATTGCCCT	84182
rs145216923	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30805062	AGAAAGTTCTCTTGT[A/G]TTTTGGGTTCTGTTG	84182
rs145225621	snp	A/G	0.0158469	0.0875917	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30809175	ACCACTTTGTTGTCA[A/G]TGTAAACAAGGGTGT	84182
rs145268990	snp	A/G	0.00557542	0.0525036	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872829	CTCAGTCACCCAGGT[A/G]ACACCAGGGAAGGGA	84182
rs145391628	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30888171	TTGCAGTGATGCCTC[A/T]GGGGGGACAGGGCCT	84182
rs145401226	snp	A/G	0.00716266	0.059414	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30854652	GTTTGGTGGTAAGCC[A/G]GAGAGTGGGAGAACT	84182
rs145412670	snp	G/T	0.00557542	0.0525036	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30848087	GAAGCTTCCAACTGA[G/T]AATTACCTGCTTCAG	84182
rs145424305	snp	A/C	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782763	GACTGTAAGGGCTGG[A/C]AAGTCTGAAATCTGT	84182
rs145451718	snp	C/T	0.00358779	0.0422022	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30870298	GCCAGTGATGCTTAT[C/T]GGCCCCCCCTCAGGA	84182
rs145496632	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30858078	AAAATGTGATTACAC[A/G]TAAGGAACACTGACT	84182
rs145515838	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852028	TTAAATCCTGCTATT[A/G]GAGTTCTCTGGGCCC	84182
rs145558209	snp	A/C	0.00318978	0.0398085	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30865250	GTAAGTGTCCTTCCT[A/C]CCCAGCATGCTAAGA	84182
rs145562976	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30774046	GAAACACACACCACT[A/G]TGTTGATGGTATCAC	84182
rs145605366	snp	A/G	0.00716266	0.059414	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30830059	AAAGGAAAGGAAGGA[A/G]AAGTCTTGTGGGGGC	84182
rs145629406	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30793555	TAAGTACGTGGGACC[A/T]CAGATGCACTTATTT	84182
rs145701532	in-del	-/CCCCCACCCCACTAAGGGGATGCGAGAGCTTCTATAT			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30843599	TTTTTGTTACCCCAC[lengthTooLong]CCCCAGGCCACATCC	84182
rs145747510	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30857005	AGGAAACTGAGGGCA[A/G]CATAAATGAAGTGGC	84182
rs145749881	snp	A/C	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836487	GTTGCTTTCCTTCCG[A/C]TAAGGGTCTGGGAAC	84182
rs145827420	in-del	-/A	0.00676609	0.0577691	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30849457	GAAAGAAATACGTAT[-/A]ATTCGGCTGTTTCCC	84182
rs145840410	snp	A/G	0.0023933	0.0345097	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840188	CCTGTGCTAAGCCCC[A/G]TGATGCCTACAGAGA	84182
rs145884921	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30816317	GTAAATTTGTTCTCC[A/G]TTCCTGGAATGTTCC	84182
rs145944716	snp	A/G	0.0023933	0.0345097	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30815955	ATGGGATAGATTAAA[A/G]TAAACCAAGATGAGA	84182
rs145961374	snp	C/T	0.00597247	0.0543191	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30883268	GCACCTCTTGAAGCC[C/T]CTCCTCCCTCAAGGC	84182
rs145973509	snp	C/G	0.00636936	0.0560724	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30886768	TCTCTGCGCTTTGCT[C/G]TGACGCAAACCTCGG	84182
rs145997890	snp	A/G	0.0134861	0.0810011	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30781389	GAAAATACTGGTATC[A/G]TTTAATTCCAAAACC	84182
rs146034554	snp	C/T	0.0119091	0.0762411	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30808271	AGTCTTTGGAACTTG[C/T]CCACTCCATTTGAGT	84182
rs146064454	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30800616	GGAGCAGTTAAGGGA[C/T]GCTATTGAGGGGGCA	84182
rs146068342	snp	A/G	0.00597247	0.0543191	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30864152	CAGTCTTGAAAGTCC[A/G]GAAGAGGTGGTAGCT	84182
rs146095391	snp	A/T	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30867272	CAGCTCCATTTCAAC[A/T]GCTCGGAGGTCTCGG	84182
rs146180317	snp	A/G	0.00874735	0.0655527	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30887777	GGCCTGGGTGCTGAC[A/G]GGGACCCGCGGGTGG	84182
rs146186301	snp	A/G	1.66829e-05	0.00288811	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782145	GAGACTACACTGGTA[A/G]ATATATATGACCTTT	84182
rs146191444	snp	A/C	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30847061	AGTGTTGGAATGATG[A/C]TTTGGGGGCATCTGA	84182
rs146194441	snp	A/G	0.00636936	0.0560724	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30880823	GACACTTGAACCGTA[A/G]GAAAGGATGAGTGCG	84182
rs146216621	in-del	-/GTTTTT			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30847734	TTTTGTTGTTTGTTC[-/GTTTTT]GTTTTTGTTTTTGTT	84182
rs146218323	snp	A/T	0.00398564	0.0444627	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850842	CTGGGGTGACCCCTC[A/T]GAGGAAGCCTCTGAC	84182
rs146242060	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30815678	GATCACTTTTCCTTC[A/G]AGAAGATATTTTTCT	84182
rs146246025	snp	C/T	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30817969	TTGCTTGCCCTCTAG[C/T]ATGTATATCACCAGC	84182
rs146311807	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30831480	CATATTCCTGTAACA[G/T]TGGAGAGAGAAAGGC	84182
rs146366707	snp	A/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30802877	CCAACCCAACCAACC[A/T]TCCAACCATCCATTC	84182
rs146372588	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30814916	TGCTTACGCAGGGGA[A/G]TGCCTTATAAGTTTG	84182
rs146409184	snp	A/G	0.00478085	0.0486577	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30812351	TCACTATAAGTGAAG[A/G]GTATATGCTGGTGTG	84182
rs146419246	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30878167	GCAGCACAGACACAG[A/C]CGTGGGAAGACTGGC	84182
rs146428325	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30774308	CACTCTGCTCTCTTT[A/G]GTGTTCTTGTGGATG	84182
rs146435356	snp	A/G	0.0356815	0.128715	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30880242	CCCTAATTGTGCTAC[A/G]TGTTCCCCCACCAGG	84182
rs146462751	snp	G/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30777509	CTCTGTTTGTTTCAA[G/T]ATTGTGTTCTTTTAG	84182
rs146495565	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30775721	ATCCACTAGTCATCA[C/T]ATTAGCATACAGAAG	84182
rs146495580	snp	A/G	0.00478085	0.0486577	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30816788	CAGATTGTTTTCACA[A/G]GATTCCAAGCAGAGA	84182
rs146508907	snp	C/G	0.00557542	0.0525036	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30861732	TGGTCCAACCGTATC[C/G]CAGGAGCTCAGATGG	84182
rs146530163	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30826717	TCCTGTGCTGCCACG[A/G]GATAGGGTTACTTGC	84182
rs146532913	snp	A/C	0.0111196	0.0737302	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30796842	CTTCATGTTACAGAT[A/C]CTTTGGTTTTGGGTA	84182
rs146544214	snp	C/T	0.00676609	0.0577691	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30860576	TGAGGGGAAGCTGCA[C/T]TCTCAGGAGGGCCAG	84182
rs146557624	in-del	-/GTC	0.0150606	0.0854603	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30831979	CTTCCTGGCCAACAT[-/GTC]GTTCTGGAGTGTTTT	84182
rs146583739	in-del	-/CCTTT	0.0640965	0.167152	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30854529	GAGGAAGAACACAGA[-/CCTTT]CCTTTCTCTCCTGGT	84182
rs146591855	snp	A/G	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30884551	CCTGCAGGTGGGCCT[A/G]TTGAGCAGGGCTCCA	84182
rs146635584	snp	A/T	0.0103295	0.0711199	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30873873	TTTACAGCAGACATT[A/T]CCTCCAAATTCTTGT	84182
rs146647310	snp	A/G	0.00438332	0.0466095	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30809440	TCCCTTAACCCAGCA[A/G]GTTTCCTAACAGGGG	84182
rs146663125	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30842504	CATATGCACCTACCT[A/G]CCTACCCACCTTCCT	84182
rs146665703	snp	C/T	0.000381151	0.0137996	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778400	GGTTTTGATTTAAGA[C/T]GGTAAACAGCGATTC	84182
rs146709199	in-del	-/T	0.00112442	0.0236843	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30781953	TATATAAATTAATGA[-/T]TTTTTTTTCTCTCCC	84182
rs146728691	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30779562	AAGCAAAGAAGGGAA[A/G]ATGCCCTATTTGAAG	84182
rs146756963	snp	A/G	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30857814	ACAGAAATTTCACCA[A/G]TACAATCTTTTTAAA	84182
rs146768131	snp	C/G	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30793578	ACTTATTTCCACACA[C/G]CTGGCTAATATTTTG	84182
rs146773527	snp	C/T	0.0023933	0.0345097	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30829459	AGTTTACCTGTTGCA[C/T]CATTTGGGCAGACAA	84182
rs146826067	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30796297	ACAGGAAACCCACAG[C/G]CATGCCATCCCCAGA	84182
rs146836551	in-del	-/GAGAGAGAGAGA			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30808933	AAAGAGGGAGTCAAG[-/GAGAGAGAGAGA]GAGAGAGAGAGAGGC	84182
rs146868745	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30879061	CATTCCTTTTCTCTG[G/T]ACCCTCAGTGGTTTT	84182
rs146880240	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839676	ATTGAGAGATTCACA[A/G]GATTTTGCAGATAGA	84182
rs146880332	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30883871	CCTGGTGTTGCTGCT[G/T]CTTGGTGTGAGCCAC	84182
rs146889300	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30774624	CATCATTCCATGGAA[A/G]TAGCTCTTCTTAGGG	84182
rs146932079	snp	C/T	0.00636936	0.0560724	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30799375	CTGAGCACCTGTGGG[C/T]ATATAGTAAATGGAT	84182
rs146940780	snp	A/G	0.00398564	0.0444627	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30862546	GGTGATTCGCAGGGC[A/G]ATGATAACAGTTCTG	84182
rs146948753	snp	C/T	0.0111196	0.0737302	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30802406	CTGGTTAGCAGAGTT[C/T]GGCTGCTTTCTTTTG	84182
rs147023351	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30885079	GACAAGGCTGAGCCC[C/T]ACCATCTCCTTGAGC	84182
rs147036965	snp	C/G	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30780059	TTGAGGAGAAGTAGG[C/G]AATGGCAGCCCCGTG	84182
rs147046190	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30889790	ATGAAGGGGAGGTGG[A/G]GTTGTGGATGAACAT	84182
rs147053047	snp	A/G/T	0.0190111	0.095823	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30783629	ATGTGAAAATCTTTG[A/G/T]GGGGGTCACTATTCA	84182
rs147056105	snp	A/C	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30848747	CAAAGAAGTGTCAGG[A/C]AGTAGCTGTTTTATT	84182
rs147139119	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30827652	GAGGATGAGGACTGC[A/C]TGGGAGGGAGGGTGA	84182
rs147190507	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30873010	ATGCGTAGCATGGAC[A/G]GGCTGGACAGAGCTG	84182
rs147199665	snp	C/T	0.00636936	0.0560724	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30877077	GGTCCCAAAGACTTG[C/T]GGGAAAAAAGAATGA	84182
rs147225713	snp	C/T	0.00795532	0.062565	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30773558	AGTGTGGTCTTCCCT[C/T]GGGGGAGTCATGATA	84182
rs147243684	snp	A/G	0.02016	0.0983543	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30811035	CCCCTAGAATTTCCA[A/G]TAAACCAGCACCAGC	84182
rs147307232	snp	C/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859797	GGTGGCCAGGAGGCC[C/G]TGGAGGCAGGGAGAG	84182
rs147330421	snp	C/G	0.00716266	0.059414	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30863010	CCCCCTCCCCAGCCT[C/G]CCAATCCAGCACCAA	84182
rs147334661	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30825612	AAGCCAGCAGCCTGG[A/G]TTTGAATCCTGACTC	84182
rs147349952	snp	C/T	0.00716266	0.059414	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30794751	CCACCTGTCACTTGT[C/T]GCTGGCTTGTCAGGG	84182
rs147352176	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859563	CAACCTGAAAGACAC[A/G]CCACCAGCCCTTGAG	84182
rs147413425	snp	C/T	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30841030	TGTTAAGGGGACTTG[C/T]GCGCGTTTGTTTCTG	84182
rs147444860	snp	C/T	0.0103295	0.0711199	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840680	ACTCTATCAGGTGGG[C/T]TCTGGGGTGGGTTTG	84182
rs147454695	snp	C/T	0.0023933	0.0345097	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30776170	AGCCAAGTGATCTTT[C/T]AAAAATATGTCAGTT	84182
rs147507290	snp	A/G	0.00159617	0.0282053	downstream-variant-500B	FAM188B, INMT-FAM188B	GRCh38.p7	7:30892566	GCCAAGTAGATGTGG[A/G]AAAAGAGCCTTCCAA	84182
rs147543793	snp	C/G	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791086	AGACATCACATCATG[C/G]GCAAATGCTTGAAGT	84182
rs147589907	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30869618	ATCTTTGGTGTCCCT[C/T]TATGTGTCCAGATTT	84182
rs147612628	snp	C/T	0.00874735	0.0655527	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30832664	ACAGGCCCGTGCCAC[C/T]ACACCTGGCTAATTT	84182
rs147622503	snp	C/T	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30835383	CCCACTCCCATGATT[C/T]GGTTATCTCTCACTG	84182
rs147665114	in-del	-/TT	0.0130921	0.0798413	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30889827	GTTATCATATACCTC[-/TT]GTCACAGGTTAGACT	84182
rs147685387	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30848923	AGACAATAGTCATAC[A/G]CGCCATTGATTGAAT	84182
rs147695086	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852104	GCTCCATTTTCTCTC[C/T]GGAGCCACCTTCTTA	84182
rs147708193	snp	C/T	0.00636936	0.0560724	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30816612	TCTCCCTCCCTCCCG[C/T]CCCCCTGCCTCCCAA	84182
rs147724589	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30820650	TTTTGAGGTTCATCC[A/G]TATTGTAGCATGTAT	84182
rs147800083	snp	C/T	0.00358779	0.0422022	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30835844	TTCTGGTGAATGCAG[C/T]GGCAGCAGGTGTAAT	84182
rs147822913	snp	C/G/T	0.00557542	0.0525036	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30838421	CAGAGGAGGTTCTTA[C/G/T]GCATGGTAGAGAGTT	84182
rs147828767	snp	A/T	0.0023933	0.0345097	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30805030	CAGACCTTCTTCTCT[A/T]GGCAATAGAGAGGGA	84182
rs147894290	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30884635	GGCCTCCGTCTGACT[C/T]TGTGTCTCTCTACCC	84182
rs147904136	snp	A/G	0.0023933	0.0345097	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30889489	CAAATAGTATCAGCA[A/G]TGGGCACTCACTGCC	84182
rs147914019	snp	C/T	0.00517822	0.0506191	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30821825	AGTTAATGATGTCTT[C/T]ACTAATCTACTGTTT	84182
rs147917592	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30783552	CTGATTTTTCACTCA[C/T]GCAAAAATTTAAAAA	84182
rs147934043	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30787845	TCTCTTTATACTCTT[A/G]AAATTATTGTGGAGT	84182
rs147986802	snp	C/G	0.00159649	0.0282165	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30891732	AATGCATCACCTGCC[C/G]CCTGGCCTCTCCATT	84182
rs148023300	snp	A/G	0.00398564	0.0444627	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30794091	CACTGCCTCAGCGAG[A/G]CGTCTTTGTGTAGTG	84182
rs148040467	snp	C/G	0.00517822	0.0506191	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30886220	GGGTAGGCCAGTCTG[C/G]TGGGCAGGTAGAATT	84182
rs148050515	snp	A/G	0.00398564	0.0444627	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30846454	ACCTGTGAGGAATTC[A/G]ACTCTTAAAGAAACT	84182
rs148051200	in-del	-/T	0.0162398	0.0886349	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30823226	AAAGATAACTTTCCC[-/T]TTTGCAATTAATAAG	84182
rs148054749	snp	A/G	0.0115144	0.0749975	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30780708	ATGCCTATGTAAATT[A/G]AGATTTTGAAAAACA	84182
rs148092900	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30784075	GCTGAAGCTCAGGGT[A/G]TGGGTGTCGAGCTGC	84182
rs148103472	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875797	ATCACAGAGGGCTTG[A/G]GAAGAAGTACAGCTT	84182
rs148125105	snp	C/T	0.00517822	0.0506191	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771729	GGGGAAACTACATTT[C/T]CCACGAGGCGTTTCT	84182
rs148157111	snp	G/T	0.00676609	0.0577691	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30870996	ATGTGTGCCCCCCAG[G/T]GTCCAGTGTGACCCC	84182
rs148167334	snp	C/T	0.00597247	0.0543191	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30834086	TCTGGAGGACAGTAG[C/T]CCTCTTCTCACAGCT	84182
rs148191490	in-del	-/A			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30796121	GTTGGAGCACTGTAC[-/A]TTTTTTTTTTTTTGT	84182
rs148220424	snp	C/T	0.00716266	0.059414	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30862165	GTTGCATGCTTCCCC[C/T]GAGGGCCTGCAGGAG	84182
rs148236722	snp	C/T	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30826970	AATTTCAGCCAGGCT[C/T]CAGTGTCGTGGTCAG	84182
rs148316052	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840636	TGCCACATCAGAGGC[C/T]CTTCTGTTGCAGAAG	84182
rs148337316	snp	A/G	0.00716266	0.059414	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30807696	TCAGTTATGTTATCT[A/G]TACATTACAGACATT	84182
rs148389073	snp	A/T	0.00517822	0.0506191	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30866244	TCCACTCACCCAGGG[A/T]CCTTACATGTTCATG	84182
rs148394781	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30824465	GATATTCAAACCATA[A/G]CAGTAAGTGATCAGT	84182
rs148416090	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30877513	CTGCGGTAGGTGGAT[C/G]CTTCCTTCCTCTGCC	84182
rs148429649	snp	A/G	0.0107246	0.0724382	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30774089	GCCACTCACCCTTGT[A/G]GTGCCTTATGGGTGC	84182
rs148439278	snp	G/T	0.00636936	0.0560724	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30838474	GTGTTTTCTGTAAAG[G/T]GCTCAATAGTGTATT	84182
rs148492667	snp	G/T	0.00318978	0.0398085	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30835224	GGGGAGGCCTCACAA[G/T]CATGGCAGAAGGCAA	84182
rs148544537	snp	C/T	0.00557542	0.0525036	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30863469	TGACTTGATTGTGTA[C/T]ATGTGCATGTGATTG	84182
rs148552879	snp	G/T	1.65704e-05	0.00287836	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828763	CGGGTGCCTCTGTGC[G/T]GTGCCCATCAGGGCC	84182
rs148605439	snp	G/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30855520	AAAAGGAAGTGACTG[G/T]TGAGGCTTCAGGGGC	84182
rs148626293	snp	A/C/G	0.0115144	0.0749975	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30842027	AAGCTTGGTACTCCA[A/C/G]TGAAACACATTTCAC	84182
rs148634521	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30818876	TGAACTTATTCATAC[G/T]AGTTTCTTCTTACTG	84182
rs148640046	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30808513	GCATGTGGTGTGAGC[A/G]TGGTGTTTTGTCTTG	84182
rs148691816	snp	C/T	0.00993419	0.0697739	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30804904	GGAAGAATCCCAAGC[C/T]GAGGGGATGCTGTGA	84182
rs148709455	snp	A/G/T	0.00637439	0.0561611	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30800620	CAGTTAAGGGACGCT[A/G/T]TTGAGGGGGCAGGAG	84182
rs148761655	snp	C/G	0.00438332	0.0466095	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30795741	TTCCTTCTGGAGCCT[C/G]TAGGGGAGAATCTGT	84182
rs148764089	in-del	-/GA	0.0785177	0.181917	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30884858	TAGTCCATGCAGAGT[-/GA]GAGTCTTAGTGTGTG	84182
rs148774381	snp	C/T	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30888928	TAGATGAGTGTGACT[C/T]ACCCCTGCACTGAAG	84182
rs148776642	snp	A/G	0.00398564	0.0444627	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30860264	GCCTGGTTGGGTCTG[A/G]TCGGCGCCCTCCCTG	84182
rs148784539	snp	A/G	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30848355	GCACTGGCTGTAACA[A/G]CTGAACTGAGGGCAG	84182
rs148954173	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30822108	AAATATTTCAGCATG[C/T]GTCTCCTAAGGGCAA	84182
rs148974244	snp	A/C	0.0182019	0.0936463	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30874779	CCCTGTTAAAACCCC[A/C]CCGTCACTAATGAAG	84182
rs149008261	snp	A/G/T	8.28293e-05	0.00643495	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778448	GCTTAAAGAAGACAT[A/G/T]TGTGACCATGGACCA	84182
rs149014343	snp	A/G	0.00597247	0.0543191	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30870458	CTCCTTCCCAGGCCT[A/G]CTGGGCTGTCTGTGG	84182
rs149041081	snp	C/T	0.00318978	0.0398085	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30802516	CCTGGAATGGGGCCT[C/T]ATTTCTCTGTCTTTA	84182
rs149089362	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30861915	CCAGAGCAACCGAGA[A/G]CATCTTGTGCTGAGT	84182
rs149092946	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30798414	AAGAGGGGGGTTGCC[A/G]TTCCCTGAAATGAAG	84182
rs149162534	snp	A/G	0.0130921	0.0798413	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30788584	GTTTTCCAAAATTCT[A/G]ATTTTTACCTGACAG	84182
rs149162796	snp	C/T	0.00597247	0.0543191	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30879789	TAATTCTTTCCTTCA[C/T]AGGGCCTCCTCTGGA	84182
rs149172586	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840422	GGTAGACAATTAACA[A/C]CCTCAACCTGTAGAC	84182
rs149246791	snp	C/G	0.00597247	0.0543191	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859388	GTTCACTGCTGCCTC[C/G]CTAGAGCCCAGGATG	84182
rs149259781	snp	G/T	0.00358779	0.0422022	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30824307	AGCCACCAATCCCAC[G/T]CCCATAACAACTTGT	84182
rs149311613	snp	G/T	0.00914312	0.0669923	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30817819	GTCTGAACAACTCTC[G/T]CATTCATTATAATCT	84182
rs149321006	snp	C/T	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30886084	CAGGAAGGGGATACA[C/T]GTGACATCGTGGCAT	84182
rs149328497	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30780273	GAGTGGACTGTACAC[G/T]TTAGGAGAATTTTGC	84182
rs149381638	snp	G/T	0.0836354	0.186609	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30810415	GTAAAAGGATTATAA[G/T]GAGGCATAAGAATGT	84182
rs149404830	snp	C/T	0.00795532	0.062565	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30863401	GTGACACTGTATGGC[C/T]GGGTGTGAGATGACA	84182
rs149411646	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30770352	CTGGTATTCCAGAAT[C/G]TGACTGTGTTGGATA	84182
rs149414226	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30800110	AGCTGACATTGACAG[C/T]AGCTGGGAAGTATTT	84182
rs149471526	snp	A/G	0.00597247	0.0543191	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30790585	AGTAGCTGAGATTAC[A/G]GTCATGCACCACCAA	84182
rs149479340	snp	A/G	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30883179	CAGGTTCAGGAGTGT[A/G]TGGTCTGCAGTGGTG	84182
rs149481134	snp	C/T	0.00755907	0.0610114	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30855359	GACCTGCTGTTGATC[C/T]GGAGTGTTGTGAGAG	84182
rs149534673	snp	C/T	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850014	AATAGCACCTGCCTG[C/T]ACGTGCTACTGACTC	84182
rs149541833	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30814979	AAGCCATGCTTTGAC[A/G]TATTTAACCAAACAG	84182
rs149554283	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872606	AAGTGCTACACAGCC[C/T]GGAGCCCAGGACACA	84182
rs149563937	snp	A/G	0.02016	0.0983543	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30835089	TATCTTTTCAGCAGC[A/G]CCCCACTTTACTGGT	84182
rs149625570	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30831228	GGAAGTTTCCCTGAG[C/T]ATTTATAGCAGAATT	84182
rs149628984	snp	A/G	0.00755907	0.0610114	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30795314	CCTGGGTGTAACTGT[A/G]GTCATGAATTGAGAA	84182
rs149661279	snp	C/T	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30816267	GTTTTGCAAACTGTA[C/T]GCCCTTGAAGAAAAC	84182
rs149709954	snp	C/T	0.00557542	0.0525036	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30877376	GTTGGGGTCATCCTT[C/T]CCTTGTAATAAAATT	84182
rs149713275	snp	A/G	0.00398564	0.0444627	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30811892	TCGGTTGTTGGAGAC[A/G]TGAGTCTTGCCAAAG	84182
rs149729805	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30774024	TAGAGCTGAATGAGA[C/T]TGGAGAGAAACACAC	84182
rs149730496	snp	C/T	0.00478085	0.0486577	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30865010	GGAGGTTTAAGTGTG[C/T]TGTTCTGAACGGGAG	84182
rs149737262	snp	C/T	0.00358779	0.0422022	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30829838	TGGACACAAGAAAAG[C/T]GGTTCCTGGTCTTCA	84182
rs149782961	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30804469	GAATGGTGTTGGGGA[A/G]AGAAATGCTGAAGAT	84182
rs149788454	snp	C/G	0.00636936	0.0560724	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791793	GAATGCTCTAGACAG[C/G]GGTGTCCAACCTTTT	84182
rs149792955	snp	A/G	0.00398564	0.0444627	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30856772	TGGAAAGGGACACCG[A/G]GACCAAGAGCTTCGT	84182
rs149797092	in-del	-/AGACTT	0.0111196	0.0737302	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30879901	AGTTGATGGTGTGTC[-/AGACTT]TGACACACCTGCTTT	84182
rs149846974	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30851401	ATGGCTGTGAGACCT[A/G]AATGAGTCAGTATAA	84182
rs149866903	snp	G/T	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30873816	ACTTGCCTGAAAAAG[G/T]CTGTGCCTTTCTCAG	84182
rs149872086	snp	G/T	0.00398564	0.0444627	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782634	CCTGAGCCCAGGAGT[G/T]CAAGGCTGCAGTGAG	84182
rs149910923	snp	G/T	0.00795532	0.062565	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30777283	GTTGACAGACATAAA[G/T]AATTATCCATCAGAG	84182
rs149922924	snp	C/T	0.00636936	0.0560724	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30841573	CCCTCCCTGCAGGCC[C/T]GGTTACCAGCTTGTA	84182
rs149943780	snp	C/T	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30832601	TCCGCCCTCTGTTTC[C/T]TGGGTTCAAGTGATT	84182
rs149948114	snp	A/G/T	0.00756386	0.061089	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30797692	GAGCCTTTGGAGGTC[A/G/T]AGCAGAGACATGCTG	84182
rs150000702	snp	C/T	0.0119091	0.0762411	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30826501	GCTTATGAAAAGATA[C/T]AGAGACATGAGCTGA	84182
rs150052131	snp	A/C	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30820530	TTCTCCATTCCTCCC[A/C]CAACCCCCAGTCTCT	84182
rs150056305	snp	A/G/T	0.00517822	0.0506191	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30888066	GTCTTGTCCTGGCTG[A/G/T]CACAGGCTCTATCAG	84182
rs150066361	in-del	-/G	0.00597247	0.0543191	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30776555	GAGTGCAAGCTCCCT[-/G]AGGACTGGGACTTTC	84182
rs150072586	in-del	-/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30807158	TGAGGATTAGAGGCT[-/G]GTTTGGCAAGGCTGA	84182
rs150087881	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30805936	CATTCACAGAGGCAG[A/G]GTGCACGGGCTTGGG	84182
rs150098444	snp	C/T	0.00478085	0.0486577	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30870055	CATCTCTCTCTCTCT[C/T]GAATGCCCTGATATG	84182
rs150106631	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30794169	CAAAGTAATCCCAAT[A/G]GTAAATATATCTGCA	84182
rs150119483	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30858459	AAGGAGTGGCAGAGC[A/G]AGGATTTAAATTAGG	84182
rs150181548	snp	C/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30849164	ACTGTGGTGGGCTGG[C/G]TTCTGGTCTGGTTTC	84182
rs150234617	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30845136	CAGGAGGAAGGCTGA[A/G]GGCTCTGAGTTTTAG	84182
rs150246045	snp	C/T	0.0023933	0.0345097	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30810153	ACACTCCAGCCTGGG[C/T]GACAGAGCAAGACTC	84182
rs150255120	snp	C/T	0.00358779	0.0422022	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30834566	CCATTGTCTTGTGGA[C/T]TAACATTTGGCTTCT	84182
rs150309240	snp	A/G	0.00358779	0.0422022	upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30769668	GAGGGGAAATTGCCT[A/G]GAGATTATGGTGCAA	84182
rs150330447	snp	G/T	0.00716266	0.059414	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30827332	TGACAGACGGGATAG[G/T]CAGGGTAGAACCGAG	84182
rs150380883	snp	A/G	0.00358779	0.0422022	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30890724	CACTGACTTGAAGAA[A/G]GACAAAGAGCCGAAG	84182
rs150399900	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30817348	AAAGCTTTTCTTCCA[C/T]GGAGAACTTGGGTTT	84182
rs150452597	snp	A/G	0.00914312	0.0669923	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30813921	ATGGGGCAGTGTAGG[A/G]TGGAAGGAAGCATAG	84182
rs150465273	snp	A/G	0.0023933	0.0345097	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30866721	CAGGCAAAGGCCACT[A/G]GTGGGGGTTTGCAGG	84182
rs150469239	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30775200	TGCAGGTTAAGTCAC[A/G]CTCATGACTGCCCCC	84182
rs150508046	snp	G/T	0.0134861	0.0810011	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30786696	ACACAATAGTCAAAA[G/T]GGGCTAAACCCCCCA	84182
rs150508355	snp	A/C/T	0.00438332	0.0466095	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30851232	CATACTCTGGGGGCA[A/C/T]GTTGGTCACTGTAGC	84182
rs150542158	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30820930	GTTTTCCACAGTGGC[A/G]CTTACTTGTGAATTA	84182
rs150562111	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30846846	GCGCAACCTAGATCC[C/T]TCGCATGCACAATTC	84182
rs150566135	snp	C/T	0.0119091	0.0762411	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30811381	GATAAAAAGCTTCAT[C/T]GCTACCTTCATTCAC	84182
rs150566787	in-del	-/ACACACACAC			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785270	CTCTCTCTCTCTCTG[-/ACACACACAC]ACACACACACACACA	84182
rs150614536	snp	C/T	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30876169	GTCTCTTCTAGCTCT[C/T]GGTGTTTTCTGGCAA	84182
rs150624121	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836957	AGTCCTTGCAGCTCT[C/T]GTTCCCTCTCCAAGA	84182
rs150686362	snp	C/T	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30799985	TGTGCCCCTCTTAGT[C/T]ATTGGCTGTGGGCTG	84182
rs150770123	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882858	TCGGGAGTGGTCAGC[A/G]CTGACCTCAGGGTGA	84182
rs150827375	snp	A/G	0.00398564	0.0444627	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30807833	ACGACCCTCTCACGC[A/G]GACTCTGTTAGAATT	84182
rs150832933	in-del	-/TG			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30772259	CTGAGGGCTGCACTC[-/TG]TGTGTTTTGTCTGTC	84182
rs150853808	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30860322	GGGGAGGACAGTGGG[A/G]GCTCTGTGGCCTCGT	84182
rs150912573	snp	C/T	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30830814	GAATGGGCAAGGTCT[C/T]GTCAAATAGCGATGT	84182
rs150937897	snp	A/G	0.0166325	0.0896639	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30838715	TGGAATCACCTGGGG[A/G]AATCTTAAAACTACT	84182
rs150967311	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30805100	ACCAGGAAGATGTGC[C/T]GCAAGGTGAGTCTAG	84182
rs151011771	snp	A/G	0.00874735	0.0655527	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30864552	CCAGCTGCATTCTCA[A/G]GAAGGTCCTTCTGCA	84182
rs151018937	snp	C/T	0.00478085	0.0486577	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30800938	CCAGCGATTTAGTCT[C/T]GTTGCCCTTGTTGCA	84182
rs151025863	snp	C/T	0.0162398	0.0886349	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30822413	TGGGCTCAAGTGATC[C/T]TCCTGCCTCAGCCTC	84182
rs151031754	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30890141	TGGACACAGTTGCCC[C/T]AAACAGTGTAACATT	84182
rs151038701	in-del	-/TG	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30812262	GAAAAATAATGTGTA[-/TG]TGTGTTGAGGGGGGG	84182
rs151089199	snp	A/C/G/T	0.0018896	0.0306807	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791564	CAGGGCAGCCAGCCC[A/C/G/T]CACCTGTCAGGTGAG	84182
rs151099522	in-del	-/TAGT	0.00557542	0.0525036	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30816981	TGCTACACATTGTGA[-/TAGT]TAGTGCACGCGATGA	84182
rs151108936	snp	C/T	0.0138799	0.0821421	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30844391	GCCTCCTCCTGGTGA[C/T]GGGCCCTGGGCAGCA	84182
rs151148658	snp	A/C	0.0023933	0.0345097	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30809037	GAGAAAGAAAGAAAG[A/C]GAGAGATATATAAGT	84182
rs151161942	snp	A/G	0.00676609	0.0577691	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30873211	GAAGGCCTCACGGGG[A/G]GTGGCTACTCTTCTG	84182
rs151209590	in-del	-/TGG			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30863424	AGATGACATGGGTGT[-/TGG]TGGTTGTGTTGGAGA	84182
rs151215372	snp	A/C	0.00597247	0.0543191	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30869018	GGATTGAAATCCCAG[A/C]AAGCTCTGCTCCCTG	84182
rs151225013	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30832244	ATCCCTCCCTGACAA[C/T]CTCAGACTAAATAGA	84182
rs151236626	snp	A/G	0.0023933	0.0345097	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30788979	AAGAGGGCCTTGGGC[A/G]CTAGTGGAGTTTGTT	84182
rs151244560	snp	A/G	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852729	AGTCATACACAATCG[A/G]GGAAATAATGGAAGA	84182
rs151245172	in-del	-/A	0.0166325	0.0896639	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30858134	CAGTTCATGGTTTCC[-/A]AAAGTGGAATGAGTG	84182
rs151297590	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30848701	GCTTGGTAACTATTT[C/T]CTCCAAGGAACATGA	84182
rs151306460	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30812826	TTCTGGTTGTTTTGT[C/T]AAAACTTCTGGACCT	84182
rs180789352	snp	C/T	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30823665	AAAGTTTCTCTAATC[C/T]TTCTAATTTACAGCC	84182
rs180801101	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30890047	ATTGCCAAAAGGCCA[C/T]ACAACCTGATTTTGG	84182
rs180801510	snp	C/G	0.00517822	0.0506191	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30779830	TCAGCAGATTGGATT[C/G]GTATGGTGGTAGGAC	84182
rs180807491	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840311	AGAGCGCAGAGCTCA[C/T]GTAACCACAGGCTGT	84182
rs180809818	snp	A/G	0.00398564	0.0444627	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30854810	TTGGGTAGGCAATGG[A/G]GCCTACCCTAGGAAC	84182
rs180816205	snp	A/G	0.0023933	0.0345097	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30808232	TGGCACTTGGAGTCC[A/G]GACATCTGAAACTTG	84182
rs180831186	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30814565	TCTACACAGGACTTT[C/T]GTGAGAATTAAATTT	84182
rs180833170	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30799739	GATGTCATGCGTGTC[A/G]AGCTTTGGGAAGCAA	84182
rs180842837	snp	A/C	0.00755907	0.0610114	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872845	ACACCAGGGAAGGGA[A/C]CTTTTCAAGATGTTA	84182
rs180843635	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30792853	CTGCTCTTATTTTTA[C/T]TATTTTCTTCATTCT	84182
rs180882218	snp	A/C	0.0189856	0.0955633	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30885673	CTGCTGGTCCCAGGA[A/C]CACACTTTGAGAACC	84182
rs180898003	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30867724	AAGTGTGGTCAAGGG[C/T]CAGTTTCTGAGAGTG	84182
rs180921240	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30804377	CCCAATAAAGTAAAC[A/G]GTTTTTGATCTCAAT	84182
rs180921626	snp	G/T	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30842905	CTGGCTCCTCTCATT[G/T]CACAGAGGCCACATC	84182
rs180930799	snp	A/G/T	0.00140696	0.0264862	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785806	ATCTAAAAGGCCCCC[A/G/T]CACAAAAGTAAGCCC	84182
rs180938178	snp	G/T	0.0023933	0.0345097	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30810668	AGTCTATAAAAATCT[G/T]ACCTTATGGTCCAAC	84182
rs180948605	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852679	GTGGGGAGGAACTTT[A/G]ATAGCATGGAACACC	84182
rs180955286	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836029	TCTGCCACTTTCCAT[C/T]TGATTGATTTGGGGC	84182
rs180957913	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30819320	GGTTATTTTGGGGGA[C/G]TGTAGAGGAGCTATC	84182
rs180963711	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30827375	TTGTTGCAGAGCAGG[C/T]GGAGGTGGGAGAAGT	84182
rs181018929	snp	A/G	0.00358779	0.0422022	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30775611	CTCTTCCCTCTCTGG[A/G]AGATTGGGAGGTAGG	84182
rs181021542	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30796003	CTGCAACCTTAATCC[C/T]CCCTTGCCATGTAAC	84182
rs181079039	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30807517	TTTAAAAAAAAAAGC[C/T]GGTCTGGTCTAAGGG	84182
rs181084371	snp	C/T	0.00724849	0.0597638	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791338	GCTTAGTGAACTGAC[C/T]GTAGAAAGGCAGAAA	84182
rs181110058	snp	A/G	0.00636936	0.0560724	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839051	AAGAAGAATGAGCCT[A/G]AAAAATAAAAAGAGA	84182
rs181111373	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30770925	CAATAAATGGCAGTC[C/T]CATTACGGGAAAGCA	84182
rs181113213	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30854259	CCTCATTTGTAAAAT[A/G]TGGGTCAGAAGAACA	84182
rs181113698	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30815650	AGTGTGTTCCAGAGA[A/C]ATGCTTCATAGAGAT	84182
rs181126519	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30822886	TGGGCTCAAGCAGTC[A/G]GCCCACCTTGGCCTC	84182
rs181132237	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30801121	CTCTCTGTGTCCTGA[A/G]GGGGAATGAATTGTG	84182
rs181393003	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30889668	TCTGCTTGACACACA[C/G]AAGCCCAGTAAATAG	84182
rs181415293	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30871857	GACTGAGGCTCAGAG[G/T]TGGAAGAGGGTTCCT	84182
rs181433646	snp	A/G	0.0107246	0.0724382	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30862936	TCACTGTGTGAAGCA[A/G]ATGCAGCGGAATGAC	84182
rs181435268	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30833069	TTCTCTACCCAGCAC[C/G]ATGTTTTTAAGTCCC	84182
rs181460205	snp	A/G	0.00109257	0.0233472	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828670	ACATTGATATTTTCT[A/G]TTTTCCAGGAAAAAT	84182
rs181476124	snp	C/T	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30858706	CATGGCTGCCTCCTT[C/T]GCCTCACCAGATCCT	84182
rs181482946	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30876363	CTTAACTAATTATGC[C/T]TGCAACAACCCTGTG	84182
rs181486635	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30844535	ACAGGTTAGGGCTTC[C/T]GTCAAGTGAAGACCC	84182
rs181560779	snp	A/C	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30848842	CTTGGTGTCACTTTC[A/C]TATTAGATGTTGGAA	84182
rs181562969	snp	C/T	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30880819	AGGGGACACTTGAAC[C/T]GTAAGAAAGGATGAG	84182
rs181586460	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30803504	GCTAATTGAGATGCC[A/G]TAGGAGCTTAGAGGA	84182
rs181596961	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30881301	GCTAGCAACGTGCTG[A/G]GGGCCCTGGTGCTTA	84182
rs181597174	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785504	GGACTTGAGGGGTCC[C/T]GTTATGGATCATCAT	84182
rs181602353	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30861998	GCAGTTCAGAGGTGT[A/G]CTTGAGAAGACACCC	84182
rs181603918	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840503	TCACAGCTGACTGGT[A/T]ATGAGGAGTCACTTT	84182
rs181605482	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30824721	TGGGATTACAGGTGC[A/G]TGACACCACGCTCAA	84182
rs181608712	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30808542	TGAAGAAGCATGGGT[C/T]AGGCACAAAGTAAGC	84182
rs181617030	snp	C/G	0.00874735	0.0655527	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30848574	AGGGCCCCCTTAGTC[C/G]TTGGTGTGGGCTCTC	84182
rs181624668	snp	A/G	0.000399281	0.0141238	splice-donor-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852280	GGAGTCTTAGAAACA[A/G]TACGACTTTCTGGAA	84182
rs181658235	snp	C/T	0.00318978	0.0398085	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30798060	GGAAACATCATAGAG[C/T]GTACTTACACTGACC	84182
rs181683531	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30885384	GGGCATGGTGGCACA[C/T]GCCTATAATCTCAGC	84182
rs181721269	snp	A/C	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30811696	GTTATGTATAGATTA[A/C]AGACATTGTATAGAA	84182
rs181726736	snp	C/T	0.00636936	0.0560724	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30873263	CTCACTCCAGGCATC[C/T]GCCTGCCCCATGGGA	84182
rs181727386	snp	A/C	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30776040	TTACCACTTCTGTTG[A/C]AAACACCTTGCTCCA	84182
rs181736198	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30867467	CATTCAGTTCTCACA[G/T]CAGTCTTTAATAGAA	84182
rs181739997	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828066	CCCTCAAAGGGTCCA[C/T]CCTTAAAAGGTGGAC	84182
rs181753594	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30811225	TACATGTATTATAGT[A/G]ACTTATACTATAAGA	84182
rs181756829	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30835795	CGGCACCATTGCCTT[A/G]GCATTGTTTCTCCCT	84182
rs181758982	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30796980	TATTTAGCAAGGACC[A/G]GCAGTATGTTAAAGA	84182
rs181786809	snp	A/G	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30814885	TCGAACATGTGGCTC[A/G]CAGCTCTTATATAAA	84182
rs181849087	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30776471	CCACCCTAGCCCTCT[A/C]TGTCTCCTTATCCTA	84182
rs181852783	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30779966	AAGTAAAGGATGGAA[A/T]TTCAGGCAAACATAT	84182
rs181963104	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30855376	GAGTGTTGTGAGAGT[A/G]CAGCAGTCACAGGAG	84182
rs182010712	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30890115	CACGGAGGAGGACGC[A/G]GAGAAAGTTTTGGAC	84182
rs182011413	snp	C/T	0.0111196	0.0737302	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30843487	CTTCACCGTGGGCTT[C/T]TGGGGGAACTTGTGG	84182
rs182036261	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30832865	CCCTCTTAACTTTCT[G/T]TCCTTATTTATCTTT	84182
rs182044558	snp	A/G	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30800324	AGGATACAGACTCCA[A/G]AAGGTGAGACTGAAA	84182
rs182076864	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30886188	CTTGTCCATCTTGCT[C/T]GGTAGGTGGGGCTGC	84182
rs182087294	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30868330	CTGTGTGACCACAAA[A/G]CCACGAGTCCTTTTT	84182
rs182146940	snp	A/T	0.00755907	0.0610114	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30863416	CGGGTGTGAGATGAC[A/T]TGGGTGTTGGTGGTT	84182
rs182151301	snp	C/T	1.7263e-05	0.00293789	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882177	AGGCCTCTCCCTCAT[C/T]CAGGTTGGCTGCTTC	84182
rs182190412	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30801494	CCTGCCATTGATGCC[C/T]GATGCTCAGCCACTT	84182
rs182193746	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30783016	CTAAACAATTGGGTA[A/C]CATAGCCTAGCCACA	84182
rs182212966	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30820812	TGAACATTTACGCAC[A/G]TGTATTTGTTTGAGT	84182
rs182214516	snp	C/T	0.00517822	0.0506191	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30806221	CTTTGAAACTTGGCT[C/T]GCCATCTTTCACATA	84182
rs182230298	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30869818	TTCTCCAGGCCCCTC[G/T]TGCTGCAGGAGGGGA	84182
rs182236775	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30838034	AGGTCTGACCCAGAG[A/G]GGGGGTACAGGGAAG	84182
rs182237969	snp	A/C/G	0.000241147	0.0109781	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853419	ACAGTTTGACCTGCT[A/C/G]TGAGGACCTGGTGAC	84182
rs182243205	snp	A/G	0.00874735	0.0655527	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30816091	TGGATTAGCCTTTTC[A/G]GCCCTTCCAGCTGGA	84182
rs182247375	snp	G/T	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30833814	TGGCCAAAACAAAGG[G/T]GCCCAGGCCCTACGC	84182
rs182308854	snp	A/G	0.00478085	0.0486577	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30858555	TCTAAGGGGGTGCCA[A/G]AAATCTCAGAAATTA	84182
rs182327701	snp	C/T	0.00874735	0.0655527	downstream-variant-500B	FAM188B, INMT-FAM188B	GRCh38.p7	7:30892717	CTGGATGGGCAGAGC[C/T]TGTGGAGCCCTCACA	84182
rs182380531	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30776888	CAGGTGTTTGTTGGG[C/G]GAATGAAGTTTGAAT	84182
rs182409351	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30856529	CAGAGTTGGGGTTTA[C/T]AGTGGGTTTCTGTGT	84182
rs182466075	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30890905	GTTCCCACCCTTCTC[A/G]TCGCAGTTCCAATGT	84182
rs182497480	snp	A/C	0.00993419	0.0697739	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30887850	CTGCAGGATGGCGGA[A/C]TGGGCAGGGCCCAGC	84182
rs182508852	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30826265	AGCCTATGACACCAC[A/G]TGACATTGCATTTAG	84182
rs182515029	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30794550	AACCTGCTGAGATGT[C/T]AGGCGGTGTGAGTAT	84182
rs182594207	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852781	AAATATAAGAGCAGT[A/G]AAGTTTTTCAGCTAC	84182
rs182597069	snp	A/C	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30845649	GAGGCAGCCCCTGCA[A/C]TTTCCTGCCTGTGTG	84182
rs182597101	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30788692	CCTGCCAAATACCCA[C/T]GCTTGAGTAACCATA	84182
rs182617013	snp	C/T	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30877378	TGGGGTCATCCTTCC[C/T]TTGTAATAAAATTGA	84182
rs182637590	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30890205	TTCAACCTTTTATGC[C/T]GAGTGTTTTAACAAG	84182
rs182655985	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30812637	ATCCGCAAGCTCTTG[C/T]ACTCCAAGGAATCAG	84182
rs182674116	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30783376	CCCATTTTAAGACTC[C/T]GAATTTAATCACATC	84182
rs182676880	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30825317	CTCTGGTGATGAGAT[C/T]TATGGGAACCCGGCA	84182
rs182684409	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30841724	TCACAAAACCGCACA[C/T]CCATGAACACATTGT	84182
rs182692386	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30856213	CTTTCTAGACCCTGA[C/T]GGCAGTTTTCAGGCC	84182
rs182695977	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30874051	TCATTTTAACGATTC[A/G]GGCGAAAACACCTCT	84182
rs182702876	snp	A/C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30841156	ATCCCTTCCACCCAC[A/C/G]AGGTCGACCTGCCGA	84182
rs182704908	snp	C/T	0.00318978	0.0398085	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30817216	GGTCATGCCAGGTGA[C/T]GTCTAAGTGCCATCC	84182
rs182706482	snp	C/G	0.0119091	0.0762411	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30874776	CTGCCCTGTTAAAAC[C/G]CCACCGTCACTAATG	84182
rs182707088	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30802004	CTGGGAAGATGTTCC[A/G]TGCAGGAGAAGTAGC	84182
rs182731948	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30774430	TTTCCCTCCTCTACT[A/G]GGTTACTCCTATCAG	84182
rs182767818	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30809495	AGGCCCGACCAGACC[C/T]AGGAGGAACCCCTTC	84182
rs182800968	snp	A/C/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30773213	AGTCATTGCACCCAG[A/C/G]AGTCGTAACCAAGAG	84182
rs182801774	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30788236	TTTCAGAAAACTGAG[A/G]TATTTTTCTTTGATA	84182
rs182827389	snp	A/G	0.0178098	0.0926698	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30820197	TGAGCCACCGCGCCC[A/G]GCCAATAATTTTTAA	84182
rs182844561	snp	A/G	0.00318978	0.0398085	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30805593	AGCCAGTCTCCTGGA[A/G]GCAGGAGGTTGCATT	84182
rs182859912	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859068	CTCTGCTGTCATTGT[C/T]ATTCAGGTTGTTGCA	84182
rs182869728	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30830139	GAGGAACAACACTCC[C/T]CCTCCACCCCAGTTC	84182
rs182913110	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30846924	GACAGCAGGCAGAAC[A/G]CAGCTTCACTGGCTC	84182
rs182925239	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30878747	AGGAAAACAGCTTGA[C/T]GGGCAAGAGTTCTGA	84182
rs182931753	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30769733	TATAGGGTGAGATAG[C/T]TGCTTCCCAAGTGTG	84182
rs182931891	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30792972	CTCTGTAAGTAATGT[G/T]TTGTCTGTATTCCGT	84182
rs182935085	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30772411	ATTTGCTACTAGTTT[A/G]CAGTGTGAACCTCAG	84182
rs182940103	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30860478	AGACCATAAGCTGCA[C/T]CACCTTCTCCCCAGG	84182
rs182943820	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30798350	GATGTGCTGTGTTAG[A/G]GAAAGAAAGGAGGCA	84182
rs183058756	snp	A/G	0.00517822	0.0506191	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30883676	GTAGCTGTCAGAAGT[A/G]CTCCCCTTGCCCCGG	84182
rs183073771	snp	C/T	0.0023933	0.0345097	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30863992	CAGACCTGGGCAGCA[C/T]TGAGCATGGGCTGCT	84182
rs183126978	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30864645	CCTGGTGTGATTGCC[A/G]TGGCCAGGCCTGGGC	84182
rs183194349	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30809312	TAACAGAAAAAATTT[A/T]AAAAATAACTGTTAG	84182
rs183214111	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30834511	CTGTGATGGGAGGGC[A/G]TGCCATGAAGACCTC	84182
rs183296968	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30887299	TGCCCCCCACACACA[C/T]CTGCCCTGTGCTGGC	84182
rs183300134	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852950	GGCCTGCCTGAAAAA[A/G]CAAAGGAGACTCCTA	84182
rs183305452	snp	A/G	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30831196	TTTCAGGACCTGCCC[A/G]AATTTCACCTGTTAT	84182
rs183378421	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30883887	CTTGGTGTGAGCCAC[A/T]GGACCTCACCTTCCT	84182
rs183385657	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850161	CACACACTTCTGGGC[C/T]CCACCAAGCCTGCAG	84182
rs183387457	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30788728	TCTGTCAGTGGTTCC[A/G]TGAAAAAACCAGCAA	84182
rs183434658	snp	C/T	0.00398564	0.0444627	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30793609	TATTTTTTGTAGAGA[C/T]GGGGTTTTGTTATGT	84182
rs183435866	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30849661	TCCTTAGAGTTCCAC[A/G]GGGTTCCACCCTTGG	84182
rs183457333	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30816584	TTTCCAGGAGGATGC[A/G]GGGCCATCCGTTTCT	84182
rs183466859	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30884298	TTTGTCCGTCCGTCC[A/G]TCCATCCGTTCGTCC	84182
rs183502823	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30796645	CGGGGAAAATAGAGC[C/G]CCAGAGAACAGAAAG	84182
rs183503010	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30834938	CATACTACTATCCGC[A/G]TTTTTGTCAAAGCCA	84182
rs183504587	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30818568	AAGCTGGACACTTGC[A/C]TCTCCTGCACAGACT	84182
rs183507179	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30775804	ACCTGGGACACAGAA[C/T]AAATATATATTTATC	84182
rs183509123	snp	A/C	0.00318978	0.0398085	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30802455	CAACCCTCAGTATAG[A/C]ACAATGATTTGATAA	84182
rs183520527	snp	C/T	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30867136	ATTTACCAAAGGTCA[C/T]GCAGTGCAGGTGGCA	84182
rs183525827	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30783167	TGGAGGTTCTGAGGG[A/G]AAAATCCATTTTCTT	84182
rs183533074	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850362	AGAACAGGCCATCTG[C/T]GGAGGGGACTGCCTG	84182
rs183534293	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30813203	CAGAGGGCTTCATTC[C/T]GCCTCTGTAGAAGAT	84182
rs183550668	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30845974	AAGAGATGAAGAGCT[C/T]TTGATCCCCCTGAAG	84182
rs183555800	snp	A/C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859562	ACAACCTGAAAGACA[A/C/T]GCCACCAGCCCTTGA	84182
rs183593955	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30830346	CCCAGCAGTGCTTAA[A/G]TGCTTTAATAAGCCA	84182
rs183598653	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30837054	GTCCCTGTGGGCACC[A/G]TTAGGGTGTGATGGA	84182
rs183625882	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30799641	ATCATCTGGGAACTT[C/T]TTAGAAACAGCTTGT	84182
rs183630761	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30779266	AAATGCAGTCTTTTT[C/T]GTTCACTATTTTATC	84182
rs183685854	snp	G/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30834085	GTCTGGAGGACAGTA[G/T]CCCTCTTCTCACAGC	84182
rs183747927	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30801841	GGCTAAAGAAGTGAG[A/G]GAGTGGCCACACATC	84182
rs183896051	snp	C/G	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30787738	GTAAAAGGGAAGTTA[C/G]GTAACCCATCTGCTG	84182
rs184008636	snp	A/C/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30891435	AAACAAAAAACTGTC[A/C/G]TGTTACTGCAGTGCT	84182
rs184050664	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836419	ACTCGGCAACATCCT[C/T]GTGGTATGAACAGAG	84182
rs184115929	snp	A/C	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839914	CAGAAAATAAGCTAA[A/C]CCCAGGATCAAGAAT	84182
rs184122441	snp	C/G	0.00119737	0.0244387	utr-variant-3-prime, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30892080	AGCTGAACCCCAAGC[C/G]TCTGGGGCAGGTCTC	84182
rs184130153	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30858206	GGGGAGCAGAAGTGA[C/T]ATGGCCGATCCCAGT	84182
rs184136125	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30854289	AGTGCCTGCCTCAGA[A/G]CATCGCGCAGAGAGC	84182
rs184140366	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30823151	TTTGTTTTATTTTGA[C/T]GATGCTAAGTTGGAT	84182
rs184150868	snp	G/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30889840	TCTTGTCACAGGTTA[G/T]ACTGGGAATGGATCT	84182
rs184161675	snp	A/G/T	0.000581755	0.0170461	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872317	CACAGGTCAGGGGGC[A/G/T]CTGTGGGGCCCAGGT	84182
rs184169033	snp	A/G	0.0119091	0.0762411	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30877877	TAGAGATGGGGTTTC[A/G]CCATATTGGCCAGGC	84182
rs184183536	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30827401	GAAGTGTGGCTGGAA[G/T]AGGCTTCTGATGGAA	84182
rs184248919	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30876019	TTCCTAGTGCTGCCT[A/C]ACAAAGTACCACAGA	84182
rs184268522	snp	C/G	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30842849	AATATTCTCAAACAC[C/G]TTCCTGAGCCCTCAG	84182
rs184290624	snp	A/G	0.00676609	0.0577691	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30891622	GTCCTAGTGGAGAGC[A/G]GCTGGTCCAGATGTG	84182
rs184305804	snp	A/G	0.000579485	0.017012	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875449	CTCCACTCTTTCAGT[A/G]ACTGATTCAGACTTG	84182
rs184332210	snp	C/T	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30843127	CCAGGGCCCTGGCAT[C/T]CAGCCCTGTGTCTGG	84182
rs184355394	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30810802	TCATATAAGAAGCAT[G/T]ACTAAATATAAAATG	84182
rs184388775	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30813896	ATTTCCTGGAGGTTC[C/T]TTTTTCATGATGGGG	84182
rs184395857	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30784467	CCTGGTCTCCAGGGC[A/T]CTAGTGATCTTCCCC	84182
rs184400681	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30807180	CAAGGCTGAGAGCCA[C/T]GTCCATTATTTCATG	84182
rs184406600	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30790872	GGTGGTGATGCAGAC[A/T]GGAGCGACGGCTTCA	84182
rs184410777	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30770726	CAGGTGACTAAGTTC[A/G]GGGAAAATGTACTGG	84182
rs184432922	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30838557	ATGGTATGAACACAG[C/T]CATGGGTGGTATGGA	84182
rs184434420	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30821980	ATTTGTTCTTTCTCT[C/T]TCTTTCTCTCATCTC	84182
rs184502382	snp	C/T	0.00358779	0.0422022	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30832025	ATGGCATTCCCACCA[C/T]GTCTGGGCCCGAGGC	84182
rs184537839	snp	A/T	0.0107246	0.0724382	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30809801	AAAAAAAAGGGGGAA[A/T]AAAAAGGGGGGCAGA	84182
rs184550878	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30795162	GAGTTTCTGGACCTG[C/T]AGATGGCCACATGGA	84182
rs184554810	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30774762	AGCTTTCCTCCTACT[C/T]CTCTGGGTGCTCCCT	84182
rs184562085	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30842212	TCCGTGGCAAGATCT[C/T]ACCTGTCCTTGTTCT	84182
rs184570293	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30826978	CCAGGCTTCAGTGTC[A/G]TGGTCAGATTTGCTT	84182
rs184702035	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30884895	GGGCCTGAACCTCCT[C/T]TTCCTCTTCTATTGG	84182
rs184702588	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30879553	CTCCCACCTCAGCCC[A/G]CACCACTCTCTCCCG	84182
rs184713508	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30847726	TGTGTGTTTTTTGTT[A/G]TTTGTTCGTTTTTGT	84182
rs184797706	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30814599	AACGTGCTTAGCAAG[C/T]GCTAGGAAAAGTAGA	84182
rs184798894	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30832355	GGGTCAGTCCTCCAG[C/T]AATCTGGAATCACTC	84182
rs184810188	snp	G/T	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30799782	CAAGCCTGAGTCAGA[G/T]TCCGGTACATGTAAT	84182
rs184811610	snp	A/T	0.00716266	0.059414	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30861694	GCTCCTGGTGGGTAC[A/T]AGCCGGGAATAATGG	84182
rs184818866	snp	C/T	0.00597247	0.0543191	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30880457	GGGCAGCTTTTTTCC[C/T]TTAATCTCTCGACTG	84182
rs184823245	snp	C/T	0.0023933	0.0345097	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30848189	TCTAGGCAGAAAGTA[C/T]ACTCCAGGCACGATT	84182
rs184826236	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30888226	CTCTGTGATTTTAAG[G/T]TGACTTGAGCACCAG	84182
rs184838346	snp	C/T	0.00597247	0.0543191	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30867577	GATTTGACCAGGGCC[C/T]TCTGACTTTAGAGCC	84182
rs184853617	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30860814	GGGACTAGGGCTGCT[G/T]CTTCCCCCTCCCTAC	84182
rs184859106	snp	A/G/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30779831	CAGCAGATTGGATTC[A/G/T]TATGGTGGTAGGACC	84182
rs184894739	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30810249	CGAAGAGTTGTCTGC[A/G]AAAGTCGTGAAAGAG	84182
rs184957116	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30885431	GCAGGAGAATCGCTT[A/G]AACCTGGGAGGCGAA	84182
rs184968220	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30775259	TTGCCACCTGAACTT[C/G]TGACCAACTAGCTAT	84182
rs184997284	snp	A/C	0.00557542	0.0525036	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30889239	GCAAAGATGATGAAC[A/C]GAACAAGAAAATTGA	84182
rs185005895	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30827295	GGGGAGGATGCCTTG[C/T]CTTCATCTCCAGATG	84182
rs185057515	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30854095	CATGGCAGAGCTGTG[A/G]TATCACAGACTCTGT	84182
rs185071847	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30795831	TTTGAAGCCAGTGAC[A/G]TTGGCTGAATCCTGC	84182
rs185098754	snp	C/T	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30870913	GTGGCTGTGTGTGCC[C/T]CCCCAGGGCCATGTG	84182
rs185099164	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30798750	TGATCCGCCCGCCTC[A/G]GCCTCTCAAAGTGCT	84182
rs185120656	snp	C/T	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836267	GGGGGAATGATCTTT[C/T]GAGTCATGCCCACCT	84182
rs185120784	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852727	TAAGTCATACACAAT[C/T]GGGGAAATAATGGAA	84182
rs185137509	snp	G/T	0.0023933	0.0345097	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30819657	ATATGTTTTGAAGCT[G/T]TGTTGTTAGGAGCAT	84182
rs185154912	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30813490	GCCCTCACCTGCTGG[A/G]TTTTCCATTCACAGC	84182
rs185155131	snp	A/G	0.00597247	0.0543191	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30867811	GTCAGGTGGAGGGGG[A/G]ATAGCTGGTTGGGTC	84182
rs185196763	snp	A/G	0.00318978	0.0398085	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30818635	GGTTCCAGAGTCCGA[A/G]TGTACTCTATTTGGG	84182
rs185219934	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785066	TATTCTCACTGTCTC[C/T]TGCCTTCTTTTTTTT	84182
rs185223356	snp	C/T	6.62965e-05	0.00575707	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778410	TAAGATGGTAAACAG[C/T]GATTCAGCTTTCTTC	84182
rs185326319	snp	A/G	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30803121	ATGTTGCCTTCTTCA[A/G]GAAGCCTTTCCTGAT	84182
rs185509592	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30851627	CGGCCCTTAGGATCT[G/T]CAGGGCAGCCCTGAG	84182
rs185524078	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875164	CTCCACAGTCTAGAC[C/T]CAAAGCACATGTCAA	84182
rs185526088	snp	A/G	0.0023933	0.0345097	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30858896	TAGAGGGCAGTAATC[A/G]TAGTACTGTCCCCCA	84182
rs185561095	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30877034	CCTCTCTGGATGATA[C/G]CCCCAGCATGCCAAA	84182
rs185644693	snp	C/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30867397	ATTCTGGTTGTTATA[C/G]TAGGAAAAAGGAAGT	84182
rs185651173	snp	C/T	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30835093	TTTTCAGCAGCGCCC[C/T]ACTTTACTGGTACCA	84182
rs185658269	snp	C/T	0.00478085	0.0486577	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30815677	AGATCACTTTTCCTT[C/T]GAGAAGATATTTTTC	84182
rs185662015	snp	C/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30870307	GCTTATCGGCCCCCC[C/G]TCAGGACCCTTTTGA	84182
rs185664266	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30801340	TGACTCTTGAGACAC[A/G]CAATACCTATTTCCT	84182
rs185666002	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30838422	AGAGGAGGTTCTTAC[A/G]CATGGTAGAGAGTTG	84182
rs185675956	snp	A/G	3.31329e-05	0.00407005	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782076	ACTCAAGATACCCCA[A/G]TCCCTGCACTCTCAG	84182
rs185679468	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30862436	AGCCTGCTCCTCTCA[C/T]GTGCCAGGCACACTG	84182
rs185679810	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30824731	GGTGCGTGACACCAC[A/G]CTCAACTAATTTATT	84182
rs185683979	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30809087	TGTACCCTATTCCTT[C/T]AAAAGCCAAGGTAAA	84182
rs185707924	snp	C/T	0.0023933	0.0345097	upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30770421	TAGGGTGGACCCTAT[C/T]CCAATACAACTGATG	84182
rs185708771	snp	A/G	0.00597247	0.0543191	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30880820	GGGGACACTTGAACC[A/G]TAAGAAAGGATGAGT	84182
rs185711059	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30841065	CGGGGAGGGTTCTCA[A/G]TGGTGCTCCACCTGG	84182
rs185718431	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30855416	GAGCCTGATGGCATC[C/T]GTGTGTGGGATCTGG	84182
rs185737050	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30806780	TGTTTGAAAGCTCTG[C/G]AGGGTGAGGCAGATG	84182
rs185746629	snp	A/G	0.0023933	0.0345097	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30793005	GTTAATACGTTACAT[A/G]TTCGTATAACTTAGT	84182
rs185755230	snp	A/C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30772537	GCAGCTTCCAAGCAT[A/C/T]GGATCTGACATATAG	84182
rs185785672	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859518	CATTCTACATATACA[C/T]GTGTCCAGGGCTACC	84182
rs185792436	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853733	GACAGCAGAGCTGGA[C/T]GGGTGGGGTCAGGAC	84182
rs185804277	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30819205	TGCCCTCTCCATATT[A/G]CTTTAACTGCTTCCC	84182
rs185810282	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30803888	CTCCACCTAAGGATC[A/G]TGGCATTTATTTAGG	84182
rs185814191	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785536	TCTGAATTTGTTTGC[C/T]TGTTTACTGGTCTTA	84182
rs185831233	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30804517	GAGGCTGAGACATCC[C/T]GACAAATATGTACTA	84182
rs185865025	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30821649	TTTTCAGGTATTTCC[C/G]TTCCTAAATTCTCTT	84182
rs185884186	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30789928	CTTCATTTCAAAAAC[G/T]AAGCAAATCTTGAGT	84182
rs185899462	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30776161	CAACCTAGCAGCCAA[A/G]TGATCTTTCAAAAAT	84182
rs185913886	snp	A/C	0.108048	0.20579	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30845715	GATGTTGCCCACCAC[A/C]TCTGGTGGGGAAATG	84182
rs185974904	snp	C/T	0.00019886	0.00996947	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785977	GATGTCTGGGCCCAT[C/T]GCCAGCTCCCCACAG	84182
rs185987404	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30792427	TTTCTATCCCCTTGA[A/G]GAGTGAGTGTAAGAT	84182
rs186112113	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30808164	CTTGCCAGAGCAGTG[C/T]GTGGCAGGCCCCCGT	84182
rs186130669	snp	A/C	0.0123036	0.0774623	upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771350	CCTCCCGCCCCAGCC[A/C]GCCAGCCCCAGGGAA	84182
rs186219525	snp	A/G/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828140	CAGAATCACAGGGCA[A/G/T]TGTTTTAAGTAACAG	84182
rs186223498	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30811382	ATAAAAAGCTTCATC[C/G]CTACCTTCATTCACC	84182
rs186226592	snp	C/T	0.00318978	0.0398085	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30797183	CCAGCACACCACCTG[C/T]GATGGCCTACTGTGT	84182
rs186238606	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30876238	GATGTATCACTCCAG[A/T]CTCTGCCTCCATCCA	84182
rs186248994	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30843597	TGGTTTTTGTTACCC[C/T]ACCCCCAGGCCACAT	84182
rs186250352	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30877428	CCATCTCCCCTCCTC[A/G]TGGGCTTCTTGGATC	84182
rs186252493	snp	C/G	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30858578	AGAAATTAGCAAAAC[C/G]TATCTTTTTTAAAAA	84182
rs186272332	snp	C/G	0.00398564	0.0444627	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30881786	TGAATTTGTTTGAGG[C/G]GTGTGGGAAGAATTG	84182
rs186330251	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30849102	CAGCCTAGGTGTAGG[C/T]CACTGGCTATGTGTC	84182
rs186382976	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30772026	CCCTTAGTCATTTTA[C/G]TCAACAGTGGGAATT	84182
rs186441335	snp	C/T	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30844836	AGAGCATCACTTTCT[C/T]CGTTTGTGAACTAGG	84182
rs186470227	snp	C/T	0.00795532	0.062565	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30776566	CCCTGAGGACTGGGA[C/T]TTTCATCTGTTCACT	84182
rs186484462	snp	A/G	0.00874735	0.0655527	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30849574	CTGCCTGTCCATTTG[A/G]TCCTACGACTGTGTC	84182
rs186492775	snp	A/C	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30812504	GGGTAATGATCATAA[A/C]GAAGTGGAACCAGGT	84182
rs186493070	snp	C/G	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30833988	ACGGCCTCCCTCCCA[C/G]TTGCTTTCATGGGCT	84182
rs186494616	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30816097	AGCCTTTTCAGCCCT[C/T]CCAGCTGGATGAGCT	84182
rs186510211	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30863511	GGAGAGGGCATAGTC[A/G]TTCCTCCCTCCTGGT	84182
rs186515558	snp	C/G	0.112983	0.209108	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882725	AAGAGTATTGTGGTA[C/G]CTAAAGTGGGACACG	84182
rs186534459	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30862944	TGAAGCAGATGCAGC[A/G]GAATGACTTTGATTA	84182
rs186538870	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30801784	TCTGCAGAGGAAAGA[G/T]ATTTCCCTTGACTCA	84182
rs186552603	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30833242	GGGCAATTTTCAAAG[A/G]AAACAAGTTTAATAG	84182
rs186597962	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30812794	TAACCAGCTGGGGCT[G/T]GAATCCTCACCCAGC	84182
rs186616344	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30798444	GACTGTGGGAGAAGC[A/T]GGTTTAGGTCATGGT	84182
rs186625428	snp	G/T	0.00318978	0.0398085	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30777010	TTTCTTTCTTTTTCT[G/T]TTTCTTTTTTTTTTT	84182
rs186637886	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30800644	GCAGGAGGGCCCTGG[A/G]CTTGGAGAGGCAGTG	84182
rs186699649	snp	A/G	8.30268e-05	0.00644256	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852326	TTTGGCTTTGTTTGG[A/G]GACTGTCTCCTTTCA	84182
rs186703984	snp	A/G	0.00953873	0.0683987	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30829107	TGGCTGGGAAGGCCC[A/G]TCCTTTTTAAAAGTT	84182
rs186708476	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30798157	TGGACAGCATGTTGC[C/T]GTATTGAATGCTATA	84182
rs186786240	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30848664	AGTGCTCCCAGCAGC[A/T]GGGGCATCCGGTTCG	84182
rs186791791	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30869836	CTGCAGGAGGGGAGA[C/T]CGAGGCCACACAGCA	84182
rs186795375	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30873413	ACAATATGAGCTGGG[A/G]CAGTCTTTTTCCCCT	84182
rs186801864	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30838317	TGAGAAAGTAGAGGG[G/T]CTGCCTTGAGAGGTG	84182
rs186805139	snp	C/T	0.000641643	0.0179	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853492	CTCCTGTGGGATGTG[C/T]GTCACTAAGCCTTCT	84182
rs186822645	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30887960	GGAACGGAAACTTTC[A/G]CACAGGCCTATTTGT	84182
rs186855677	snp	C/T	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30814907	TTATATAAATGCTTA[C/T]GCAGGGGAATGCCTT	84182
rs186863835	snp	C/T	0.00438332	0.0466095	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30780400	TCTTTGACATTCAAG[C/T]TATTTTTATTCCCTC	84182
rs186922336	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30834804	CTCTCTCAAGTTTAA[A/T]GTTCTGCAAATCTCT	84182
rs186924545	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30874079	TCTATAAACTCTACC[C/T]TCCAGAGTTTACACT	84182
rs186926771	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30841286	TCCACTCCCTGCAGC[C/T]GTTCAGTTTCCATTT	84182
rs186931143	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30818051	GCAGGGATGCTTCCA[A/G]TGCCTCAGCGTTAGG	84182
rs186936584	snp	A/C/G	0.0119091	0.0762411	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30802172	TTAGCTATGTTCCAG[A/C/G]AGTTCCTGGCTACCA	84182
rs186956385	snp	C/T	0.00636936	0.0560724	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30890428	TTGTTCCCAAATGGG[C/T]TGCATGCAAATAACT	84182
rs186994174	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30783575	TTTAAAAAATTACAA[C/T]CTCTGGCATAAATGA	84182
rs187068766	snp	A/C	0.0023933	0.0345097	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30820355	TTCTTTATATAATTT[A/C]TCCTCTTTTCTTGCT	84182
rs187069992	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30837803	GCCTCTGGAAAGCAG[A/G]GTCCAGGTTCCCAGG	84182
rs187080174	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30805876	GAGAGATTTGTGCAT[A/G]TTTGTGAGCCATGTT	84182
rs187097791	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853156	TTCTGGGGTCTCAGG[C/T]CCAGAGCTGCCGTAG	84182
rs187102239	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30886416	AACCCAGCTCTGTTG[C/T]CCTGCAAGAACCCCC	84182
rs187113197	snp	A/G/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852806	AGCTACCTCTTGCCA[A/G/T]CCTCTTCACTGAGAA	84182
rs187139507	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30788375	TTTTTACCCCTGAAT[C/G]ATTTAGTAACATAAT	84182
rs187150206	snp	G/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30787922	TTTGAAATTAAAAGT[G/T]AGAAGTTAAAAATAT	84182
rs187174703	snp	A/G	0.227369	0.248974	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30820059	GGCGCCCGCCACTAC[A/G]CCCGGCTAATTTTTT	84182
rs187178353	snp	C/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30879201	GGCCTTTAAGGAAAT[C/G]ATTAAGGTAAAATGA	84182
rs187232659	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872907	CTACACCTGGCTTCT[A/G]TCCATGCCTTTCTCC	84182
rs187284649	snp	A/G	0.00159617	0.0282053	downstream-variant-500B	FAM188B, INMT-FAM188B	GRCh38.p7	7:30892724	GGCAGAGCCTGTGGA[A/G]CCCTCACATTCCAGA	84182
rs187290094	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30868779	GGGCAAAGCTCTCTA[C/T]TCCTCCTTCTCTGTC	84182
rs187353402	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840342	TGAAGGGGCTCACTG[A/C]CAGCCGAGATGGTCA	84182
rs187364305	snp	C/G	0.00318978	0.0398085	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30808378	TGATACTTTGGTTTT[C/G]GTTTTCACATGGCTT	84182
rs187366942	snp	C/T	0.00824959	0.0636926	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836700	AAGAGGTCATCCTGT[C/T]GCCAGTCCCATCAGT	84182
rs187377458	snp	A/G	0.00993419	0.0697739	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30809916	GGCGCAGTGGCTCAC[A/G]TCTGTAATCCCAGCC	84182
rs187380536	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30795338	TTGAGAAGAGTTTTA[C/T]CCTCCCTTAGGAATT	84182
rs187382054	snp	C/G	0.00755907	0.0610114	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30805183	GCAAGTGGGCTCTGG[C/G]CTGGATGTGCCAGAG	84182
rs187390427	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30774841	TGGGCTCAAGGACTT[A/G]GTTTATGGCTCTCTT	84182
rs187438925	snp	C/T	0.00755907	0.0610114	upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30770203	AGAATGGTTTGAATC[C/T]GGGAGGTGGTTGTTC	84182
rs187462678	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30890092	CATCACTGAACATCA[C/T]CAAATGACACGGAGG	84182
rs187464159	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30830143	AACAACACTCCTCCT[C/T]CACCCCAGTTCATTT	84182
rs187466713	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30854848	GGCAGGTGAGGTCAC[C/T]GGAGGGGCAATCCAC	84182
rs187467461	snp	A/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30806343	GGCAAAGGCAAAAAC[A/T]TTTTAGCCTCTTTTA	84182
rs187577412	snp	C/T	0.00755907	0.0610114	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30792940	TCTTTTGTAATATGT[C/T]TTAAAGCTGCAAATT	84182
rs187618118	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30823805	TTGTTTTGAGCATAT[A/T]TTAGTAGGACTTAAA	84182
rs187644780	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30883690	TGCTCCCCTTGCCCC[A/G]GCAGGCCCTTCACAA	84182
rs187644951	snp	C/T	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30842389	GCTCTCCCTGGTGGG[C/T]TCAACACAGTCCTGT	84182
rs187652541	snp	C/T	0.02016	0.0983543	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30857744	GTGAGCCACCGCGCC[C/T]GGCCATATCCACCTT	84182
rs187664843	snp	C/T	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30827060	GGTGACACTAAGGGT[C/T]GGGAAACCAGTTCGG	84182
rs187667756	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30891521	TTCCTGCCAGCTTCC[C/T]GGCCCCTCCCCACCC	84182
rs187679422	snp	G/T	0.00358779	0.0422022	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875240	ATAGGACAGGGTCCT[G/T]TGAATGGTTGGTACT	84182
rs187700280	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30821563	GTCTAGGTATGCATT[C/T]ATTTTTACATGTCCA	84182
rs187724531	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30789226	TCCTGATCATCAAGC[A/G]TGTCCAGTGGAGATG	84182
rs187796134	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30884342	CCCCCTGAGCCAGGG[A/G]TGAAGCATTCTTGCA	84182
rs187799171	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30846274	TCTGTACATGGCTCC[A/T]TGGGCACGTCACAGT	84182
rs187817723	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30830487	TGGCTGGGGAGGCCT[C/T]AGGAAACTTACAATC	84182
rs187834203	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859573	GACACGCCACCAGCC[C/T]TTGAGGAGCTTGCCT	84182
rs187874992	snp	C/G/T	0.00398691	0.0444912	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30813372	GAATTCTGTGTGAGG[C/G/T]GGGCCTTGTGCTCCC	84182
rs187882848	snp	C/T	0.00478085	0.0486577	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30798641	AGCTGGGACTGCAGT[C/T]GCCCGCCACCACGCC	84182
rs187915532	snp	A/G/T	0.00159649	0.0282165	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30884011	GGTGTTTGTGCTCAC[A/G/T]ATGATGACCTCAGCC	84182
rs187919735	snp	C/T	0.00557542	0.0525036	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850191	GAGCCCTCTTTGCTC[C/T]TGTGGGCCCTTTCCT	84182
rs187956028	snp	G/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30794611	CTCCTCAGATCTGAC[G/T]CCGGGAGCTGAAGGG	84182
rs187964913	snp	A/G	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30825450	TCCCACCATCTCAGC[A/G]GGCTCATGGCCACCT	84182
rs187966221	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30774708	TTTGTCACAGTTGAT[C/T]GTGTCCTTCTGCTTG	84182
rs187978724	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30793732	CTGCCCGTGGAAGAG[A/C]AGCCCACTTCTAAGA	84182
rs187983728	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30779327	GTGAAATATATTTGT[A/G]GAATAAATGAATGAA	84182
rs188045001	snp	A/C/T	0.000546394	0.0165198	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778474	GACCAGGAACGCCCA[A/C/T]GCTCTGACCTCAGCA	84182
rs188060588	snp	G/T	0.0023933	0.0345097	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30869396	GCATTTGAAGAAAGG[G/T]CTCTGAATCTAAAAA	84182
rs188062564	snp	C/T	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30847129	GGCCAGGGAGGGCAA[C/T]GGTTTTACCAGAACC	84182
rs188078023	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30813679	CTCAGGGACACAGCT[A/G]ATTTTAGCCCAGGGT	84182
rs188179506	snp	A/C	0.0023933	0.0345097	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30801902	TTGTCCATCTGTGGA[A/C]ATCAGCATGGCAGCT	84182
rs188192187	snp	A/C	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30865611	CTGGAGACCCTGTGC[A/C]GACACCTGAATCTGG	84182
rs188202636	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30834319	GCTCAACACCACATG[C/G]TAGCTGCCAAAGCTT	84182
rs188219485	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30773797	CCATCATAGCCCCAC[A/G]TAAACTCTTCTCCAG	84182
rs188245454	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30809353	ATTGTGAGCACACCT[C/T]ACCAGTTCAGAAGTA	84182
rs188278302	snp	C/T	0.00358779	0.0422022	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30860532	TCATTTCTGGGCTGA[C/T]GGGTTGGGTGGGAGT	84182
rs188302653	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30832053	GGCCTGCTATATGGT[C/T]CTAAACCAACTCCCT	84182
rs188315181	snp	A/C	0.00557542	0.0525036	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30799021	GTTAGTAGGGTTGCT[A/C]ACAGCTACTGTCTAA	84182
rs188318337	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30814087	GGAGGACCAGCGTCA[C/G]GTTCAGAAGCAGAGT	84182
rs188322132	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30799717	GGTTTTAACAAGCTT[C/T]TTAGGTGATGTCATG	84182
rs188341121	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30831552	TCCAGAGGCTGGACC[A/G]GCATGGTGGGTGAGA	84182
rs188347220	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30887424	CTGAGCTGCTGTGAG[A/G]TTGAGAGAAGAGCTG	84182
rs188388760	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30890036	GAAAAGGATTGATTG[A/C]CAAAAGGCCATACAA	84182
rs188399050	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30854391	TGTAATGATGCTCTA[A/G]GGGCAGCCTTGAGAT	84182
rs188475146	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30783226	TGTGCCTTGACTCTT[A/G]GCCCCTTCTTCCATT	84182
rs188495418	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30849842	TATCTCCAGCTACCT[C/T]TTCCCAGCCACATTG	84182
rs188501454	snp	A/G	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30817007	CGCGATGACTTCTCG[A/G]TAACCCAACCCTTCA	84182
rs188537926	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30891902	AAGAGATGGGCTCTC[A/G]TCTGGGACCCTGAAG	84182
rs188539671	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852678	TGTGGGGAGGAACTT[C/T]AATAGCATGGAACAC	84182
rs188541952	snp	A/C	0.00993419	0.0697739	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30858121	GGTGTCTTCAGTCAC[A/C]GTTCATGGTTTCCAA	84182
rs188546124	snp	C/T	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30864227	GAGGGTGAGGGATGA[C/T]GCTGGGCAGGACCCA	84182
rs188549827	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30819257	TTTTAATGTTAACCA[C/T]TTTGAAATATTTTCT	84182
rs188551834	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30835957	CTGGAATATGGCTTA[C/T]GGTCCCTGCTGGAGG	84182
rs188552156	snp	C/G	3.44828e-05	0.00415213	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875661	ACATGTGCCAGGTAC[C/G]CAGATGCTCACGTTC	84182
rs188566495	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30867595	TGACTTTAGAGCCCA[A/G]GTTCTCTTGGTTGTA	84182
rs188613291	snp	C/G	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30804261	ATTCTACTTTGTTTT[C/G]TCTACTCATTCCACA	84182
rs188621654	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785577	CAGACTTGCCTTGAT[A/T]CCAGAGTATTTTCTG	84182
rs188647213	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30888466	GGCTGGCTGTCAGCC[A/G]CCTCCTGCATTAGCA	84182
rs188682721	snp	C/G	0.00398564	0.0444627	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30838785	GCTGGTGTGTTTTCT[C/G]AACATCAAGATTGTT	84182
rs188689132	snp	C/T	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30854235	CTGAATCCTTCTGTA[C/T]CTCACTTTCCTCATT	84182
rs188698827	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30821997	CTTTCTCTCATCTCC[G/T]CCTCCCCAATATATA	84182
rs188717110	snp	C/T	0.00318978	0.0398085	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30871084	AGGGCTGCATGTGAC[C/T]GCCAGGTTCAGTTGT	84182
rs188753821	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30807181	AAGGCTGAGAGCCAC[A/G]TCCATTATTTCATGT	84182
rs188767939	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30790922	CTCTGTAAGGGCTGC[A/G]AGAGAAAGGCCCAGG	84182
rs188773309	snp	A/G	0.00279162	0.0372561	upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30770849	ATGGGGCCAACAGTA[A/G]CTACCTAGCCAGGAA	84182
rs188788189	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30874997	TTAAAAAATAACATC[A/G]TTTAAGACTCACCCA	84182
rs188837949	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30809524	TCAGGACAGGACCAT[C/T]GATGGTTCCTCCCAG	84182
rs188870980	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30841949	AGGTGTTACCCAGAC[A/G]ACAAGACCCATTTCC	84182
rs188912880	snp	C/T	0.0023933	0.0345097	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30783048	TTTTAATCCTCACAG[C/T]AGTTAAAGCAATACC	84182
rs188920871	snp	A/G	0.0023933	0.0345097	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30870411	TAGCGCCAGCGAAGC[A/G]CTATGCTCTGCCATG	84182
rs189003029	snp	C/T	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30838428	GGTTCTTACGCATGG[C/T]AGAGAGTTGTACTAG	84182
rs189038200	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30858700	CATCTACATGGCTGC[C/T]TCCTTCGCCTCACCA	84182
rs189046097	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30876307	ATACAGACCTCAGTC[A/G]TATTGGATTAAGGGC	84182
rs189047717	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778183	ATGTAGGGCCAAACC[C/T]AGGACTCCTGTGCGC	84182
rs189078487	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30890907	TCCCACCCTTCTCAT[C/T]GCAGTTCCAATGTCA	84182
rs189140619	snp	A/G	0.00874735	0.0655527	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30856763	GGCTTTCTATGGAAA[A/G]GGACACCGAGACCAA	84182
rs189185381	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30861971	ATGGGACCAAGCCCC[A/G]CCCAGGGGCATGCAG	84182
rs189191827	snp	C/T	0.00398564	0.0444627	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30880467	TTTCCCTTAATCTCT[C/T]GACTGTTACTTCTGC	84182
rs189204426	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30848267	GTAGGAAGACACGCC[C/T]CCACCCCCACCCCAT	84182
rs189259605	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30832452	CCTCCAGAGAACATT[C/G]TCAATGTTGGTCTTT	84182
rs189259716	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30814790	AAGTGTAAGCCTCTT[C/T]ACCTTTCTAAAAGTA	84182
rs189327628	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30867201	GTCTACTCCCTCTTG[G/T]CCATCCTGGGAAAAC	84182
rs189336114	snp	A/G	0.00636936	0.0560724	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30811070	AGATCACTTCTTATC[A/G]AAGGGTGGAAAGAAA	84182
rs189338862	snp	C/T	0.00159617	0.0282053	upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771352	TCCCGCCCCAGCCCG[C/T]CAGCCCCAGGGAAGG	84182
rs189341777	snp	C/T	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30834961	CAAAGCCATTCAACA[C/T]GTCTCTAGGAAGTTT	84182
rs189347865	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840155	CTAGCCTTTGCCAAT[A/G]TGTCCCAGGAGTCAG	84182
rs189348045	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30851063	CAGTTATCCTGACCC[G/T]CATCGTCTCTTCACC	84182
rs189367654	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30808178	GCGTGGCAGGCCCCC[A/G]TGGAGGATCAATGTG	84182
rs189371570	snp	C/G	0.00318978	0.0398085	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30861002	ACGTGGCCACACACA[C/G]AGACACACACACACA	84182
rs189383061	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30790515	ACAGTAGTGTGATCT[C/T]GGCTCACTGCAATCT	84182
rs189401469	snp	G/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30796819	TAACCAACATATGAT[G/T]TCTTGCTCTTCATGT	84182
rs189407581	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30818570	GCTGGACACTTGCCT[C/T]TCCTGCACAGACTTT	84182
rs189409633	snp	C/T	0.00597247	0.0543191	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30775871	TCCTACAACTGTGCC[C/T]ATTGGAATAAATGGC	84182
rs189420478	snp	C/T	0.00279162	0.0372561	downstream-variant-500B	FAM188B, INMT-FAM188B	GRCh38.p7	7:30892456	TGTCTGTGCTGATCA[C/T]GGCTGGTATGGAGAA	84182
rs189443953	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30770427	GGACCCTATTCCAAT[A/G]CAACTGATGTCTTTA	84182
rs189471175	snp	C/T	0.00835141	0.0640778	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30885443	CTTGAACCTGGGAGG[C/T]GAAGATTGCAGTGAG	84182
rs189481254	snp	C/G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30795904	TCTGCTTTTGAGGAC[C/G/T]TTTGTGATTACCTTG	84182
rs189514926	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30827324	TGAAACAGTGACAGA[C/T]GGGATAGGCAGGGTA	84182
rs189573355	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30815048	TCGTTGGTGCAGCTT[A/T]CTTCCCTGACACGTT	84182
rs189618038	snp	A/G	0.00636936	0.0560724	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30792639	GTTTTAAATTTATTG[A/G]TATAAAATTGTATAA	84182
rs189627232	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30848721	AAGGAACATGATGGG[C/T]TTCCTGAGGCCAAAG	84182
rs189638858	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30879815	CTGGATTTTAAGCAT[C/T]GCATTTCATCGCCTT	84182
rs189646481	snp	A/T	0.0031936	0.0398322	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30823509	GTAGCAGACTCATGA[A/T]TTTTTTTCAATATTT	84182
rs189648809	snp	G/T	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30847909	CCTGGCTGATTTTTT[G/T]ATTTTTCTAGACAGA	84182
rs189760878	snp	C/T	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30775330	TGTGCTAGAATGGCT[C/T]ACAGAACTCGGAGAA	84182
rs189781393	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30842864	CTTCCTGAGCCCTCA[G/T]GCTCTGTGCTCAGGC	84182
rs189782037	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30890547	TCAAAGGGAAATGGA[A/G]TGGTGTAAAGTATTC	84182
rs189791793	snp	A/G	0.00438332	0.0466095	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30810340	CCTGAATGTAAAACT[A/G]TTGAAAAAAAAAAAA	84182
rs189801591	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30885821	GGCTCCATTAGCTAT[C/G]CCCTCATCCCCAGGT	84182
rs189803492	snp	A/T	0.108048	0.20579	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30845716	ATGTTGCCCACCACA[A/T]CTGGTGGGGAAATGG	84182
rs189809813	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30830220	CGCATATGCAAGGCT[C/T]GGTAGAAGGCAGACC	84182
rs189818363	snp	C/G	0.00636936	0.0560724	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30868182	TGAGCCAGCAATGGT[C/G]GGGGCTAGGGGTAGG	84182
rs189848703	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30874413	GTGTGGCTTGAGTAA[A/C]CCACCTGTGAGCCCC	84182
rs189869860	snp	C/T	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30889327	ATGTAATAGATGAAC[C/T]CAGTACCCAGGAGCT	84182
rs189876689	snp	A/G	0.00478085	0.0486577	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30862703	AAGCCCAGTGAGGTG[A/G]CAAGTCACAGGAAAG	84182
rs189913989	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30869582	CTGAGTCCTCACTTC[A/G]TCTTTTCCTTGTGAG	84182
rs189934119	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853239	TACAGGTATGGCCGT[A/G]CCTCTCAGCCCTGAC	84182
rs189948943	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30849363	AGACCAGCTAGCTTC[C/T]GTATGAGTTTTTTAA	84182
rs189953213	snp	A/C	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30881140	GCCTGGCCCGTGGCA[A/C]GTACATAGCTGGATA	84182
rs189970445	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30833274	GAACTCACAGTTCCA[C/T]GTTGCTGGGGAAGCC	84182
rs189991626	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30837917	ACCAGCCCACATTTG[A/G]TGACATGTGGACAAA	84182
rs190025412	snp	C/T	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30815720	AACATCACATCTACC[C/T]ACCCTTTCACTGCCT	84182
rs190028632	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30801368	CCTTTCCAGCATGCC[A/G]GTCATCCTGTGTGGA	84182
rs190037844	snp	A/G	1.66114e-05	0.00288192	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782125	AAGTGCCATCAAGAT[A/G]CTCAGAGACTACACT	84182
rs190140763	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30825221	AACTGACCTTTTAAA[C/T]TTTGTAAAGCTTATG	84182
rs190145016	snp	A/G	0.00318978	0.0398085	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30809113	GTAAATTTAAAACCT[A/G]TAATTGATGATTGAA	84182
rs190146380	snp	G/T	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30803289	GTGTCCCTACCTTTT[G/T]GAGTTTTGCTCAGAA	84182
rs190149037	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30793540	CCCACCTTAGCTTCC[C/T]AAGTACGTGGGACCA	84182
rs190173123	snp	A/C	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30867453	TATATAGTTCATCTC[A/C]TTCAGTTCTCACAGC	84182
rs190174998	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30835263	AAGTCACATCTTATG[C/T]GGATGGCAGCAGGCA	84182
rs190291380	snp	A/G	0.00318978	0.0398085	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30821724	AGAAGTTTTTCCTCC[A/G]TTTCTCTTATTTATT	84182
rs190335188	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30799804	ACATGTAATTTGTTG[A/G]GGGCATGCTCTCAGG	84182
rs190358286	snp	A/G	0.00438332	0.0466095	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30885216	CTTCAAGCTTCAGGG[A/G]CATCAGAGTCACCTG	84182
rs190391463	snp	A/T	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30818932	TTTTATCCTTCCTTT[A/T]CACTCTTAGTATTGT	84182
rs190392890	snp	G/T	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30843422	GGCCCTTGCAGGAGA[G/T]TGTCTCTAAACTCAT	84182
rs190407335	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785184	GTAGGTCAGAAGCAC[A/C]TGCCATCCACCCTCT	84182
rs190414264	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30876045	ACAGACTGGGTGGCT[C/T]GAAACAACAGAAACT	84182
rs190416640	snp	A/G	0.00438332	0.0466095	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30851922	CAGTTGTGGGTGAGA[A/G]TCAGACTTCCTACTG	84182
rs190440676	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30784611	TTAGAATACAAGCCC[C/T]GGCTGCTCCCCTGAG	84182
rs190459373	snp	A/G	0.0023933	0.0345097	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30873575	AGATTCTCAATTTCT[A/G]TCAGGCTCCCCAGGG	84182
rs190465700	snp	C/T	0.00636936	0.0560724	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30841073	GTTCTCAGTGGTGCT[C/T]CACCTGGGAAGGGGC	84182
rs190470692	snp	A/C	0.0023933	0.0345097	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30855546	GGGGCTAAGGTGGAG[A/C]CTGAGGGTGATTGCT	84182
rs190491752	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30890196	TCCACCTGTTTCAAC[C/G]TTTTATGCCGAGTGT	84182
rs190536202	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30779935	GGGAGGAACCTATGC[C/T]AGGCATCTCTCAATA	84182
rs190543048	snp	C/T	0.00755907	0.0610114	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30807040	TGTCACTTTGTTTAG[C/T]CTTTCTTCTTTAAAT	84182
rs190640731	snp	C/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30827939	ATGGGTTTTCAGAGA[C/G]TGATGTAATATTGTT	84182
rs190682136	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30788173	TATGAAGAAAATCTA[A/G]CCTCACACAGATAAG	84182
rs190682329	snp	C/T	0.0023933	0.0345097	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828377	TTGCAGTGAAATTGG[C/T]GAGATAGCCTACATG	84182
rs190684804	snp	C/T	0.00874735	0.0655527	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30858440	GTTTCCATGGTCACA[C/T]AGCAAGGAGTGGCAG	84182
rs190688659	snp	C/T	0.00358779	0.0422022	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30811416	ATGCTTCAGCACAAG[C/T]GTACTATATCAGTCA	84182
rs190697015	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30797383	GACAGGGAGCCCTGG[A/G]GACAGAGCTGCTATT	84182
rs190724637	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30802501	ATGAACTTTTTGAGG[C/G]CTGGAATGGGGCCTT	84182
rs190769382	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30808460	TAAAAGTGTGTGTGT[A/G]TGGGTGCCCTTTTTA	84182
rs190778280	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30877466	ACCCTCTGCTGTTCT[C/G]TGCTCAGCTGAGGAC	84182
rs190819245	snp	A/G	0.00318978	0.0398085	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30792952	TGTTTTAAAGCTGCA[A/G]ATTTCTCTGTAAGTA	84182
rs190831795	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30772074	TTTTGTAAGTTTTCC[A/T]ATTGTCTTGTCCCAG	84182
rs190835257	snp	A/G	0.00597247	0.0543191	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30883592	GGAGGGGAATGTTCA[A/G]TAACTGGGGTGAGTT	84182
rs190851578	snp	C/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30863783	CAAAGCCTTGTGAAG[C/G]TTTTTTTTCCACTTG	84182
rs190887403	snp	A/G	0.00557542	0.0525036	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30809476	AATCTTAATTACCAT[A/G]CAAAGGCCCGACCAG	84182
rs190913839	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30834007	CTTTCATGGGCTGGT[A/G]TTGAGTGTCTGTGGC	84182
rs190919759	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30863257	CTGAGTCTCCAGGAC[C/T]AACTGCAGTTCAGCT	84182
rs190920311	snp	A/C	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30849651	CTCCGCTGATTCCTT[A/C]GAGTTCCACAGGGTT	84182
rs190928981	snp	A/G	0.00358779	0.0422022	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30841685	CACAGTAGTTATACT[A/G]TGTGTGTTCTGCTCA	84182
rs190991210	snp	A/G	0.0023933	0.0345097	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859528	ATACACGTGTCCAGG[A/G]CTACCATGTGTGTGG	84182
rs191044572	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30798338	GTGTATGGATTGGAT[A/G]TGCTGTGTTAGAGAA	84182
rs191060068	snp	G/T	0.000238237	0.0109115	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30858980	GGAGCTGGCCATGAC[G/T]GTTGCTGTCTTGTGA	84182
rs191062326	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30812979	AGCGCTCTTCCTGGC[A/G]TCTGCCTTGCTTGGG	84182
rs191064523	snp	C/T	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836367	TCCACTCTATGTCCA[C/T]GCGTGGAACTTTCTA	84182
rs191068430	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852728	AAGTCATACACAATC[A/G]GGGAAATAATGGAAG	84182
rs191068655	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30798527	TTTGAGACAGAGTCT[C/T]GCTGTGTCGCCCAGG	84182
rs191073346	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30829835	GTTTGGACACAAGAA[A/G]AGCGGTTCCTGGTCT	84182
rs191079007	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30777911	TTCTGGCAGTTCAGG[A/G]TGGGATGATGGAAAG	84182
rs191134235	snp	A/G	0.00358779	0.0422022	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30826091	TCCCTTTACCTCTTT[A/G]TGATAAGGATTCTTA	84182
rs191148591	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30794397	GCACAGAGCCAGCTC[A/C]ACCGCTCTGTCCTAA	84182
rs191151795	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30856247	TGCCTTGCCTGACCT[C/T]GCCTTTCAATGCAGG	84182
rs191172041	snp	C/T	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30881941	GGGGGCGAGTGATAC[C/T]GGGTCTCAGGTCTGT	84182
rs191199383	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30888026	TGCTTTTCTACCAGT[C/G]AGGAGCTTTGAACTC	84182
rs191203650	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30861189	CCCTGCTATGGTGTT[C/T]GGGCCAGGCAGGCAG	84182
rs191239811	snp	C/T	0.00557542	0.0525036	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30877294	GTTTCATTCTTGGGT[C/T]GAGGGCGTTGGTCAG	84182
rs191267992	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30870209	CTGACGCAGGCTCTC[A/G]AGCCCGCTGGGTGAA	84182
rs191268021	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30832300	TCACTTTGTGCCTCC[A/G]GGAAACAATCTGGCT	84182
rs191285676	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30812584	GCTAGCCCAAAACAC[A/G]CTGAGGGAGCAGCTG	84182
rs191319914	snp	A/G	0.0123036	0.0774623	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30845571	CTTCAGGAACACCAC[A/G]ATGACCTGCCATCAG	84182
rs191330657	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30866837	GGGCTTTGGCCAGCT[A/G]CTGATGAGCCTGGGC	84182
rs191344969	snp	A/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850321	GGGCTCCTGGGCTGC[A/T]GGTGGCCCCTCTGCA	84182
rs191350691	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30776629	GTGGTCTGTTCCCTT[C/T]GTTTCACAGATAGGG	84182
rs191386823	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30784339	GAGTCCTGTGAGCTC[C/T]TCACCCAGAGTGATA	84182
rs191412754	snp	C/T	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30818235	AATTACATTATTAGA[C/T]TTTCTACTGTTAAAA	84182
rs191414386	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30834866	TAGAACACAACAAGA[A/G]TCACCTTTGCTCCAA	84182
rs191428207	snp	C/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30802178	ATGTTCCAGCAGTTC[C/G]TGGCTACCAGAATCC	84182
rs191431276	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30773171	TAGGGCAGAGACCAC[A/G]TGCTCCCCACAGGGT	84182
rs191438690	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30800943	GATTTAGTCTCGTTG[A/C]CCTTGTTGCATAATT	84182
rs191511671	snp	A/G	1.65625e-05	0.00287766	utr-variant-3-prime, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30892019	GACCGTTGGATGTGG[A/G]TAAACCCTGTGGTCC	84182
rs191528689	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30788488	TCACACCAAAAAATT[G/T]CATTCATTGATGTCA	84182
rs191538918	snp	C/T			upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30769676	ATTGCCTGGAGATTA[C/T]GGTGCAATCTGCCAC	84182
rs191562513	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30820501	AGGAAAATCCTTTAT[G/T]CATTAAGCAGTTTTT	84182
rs191567332	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30806103	GTCAATTCTACTCAG[C/T]AGAGTTGTTGAGTTA	84182
rs191702079	snp	C/G	0.000100299	0.00708093	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836787	TAAGGAGACTCCTGG[C/G]TTAAATGTGTCTTGA	84182
rs191709157	snp	C/T	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30805513	AGTGGAGACCACGTG[C/T]TTGGTGTGGGGCAGG	84182
rs191713133	snp	A/C	0.00993419	0.0697739	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30783361	GGCCCACCAGATAAT[A/C]CCATTTTAAGACTCC	84182
rs191734406	snp	A/G	0.00478085	0.0486577	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30869297	GGAGATCCAGGGGCT[A/G]ATAGAGGAGGAGAAG	84182
rs191740246	snp	A/G	0.00636936	0.0560724	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30776438	CACCTTTGATAAAGT[A/G]GCAGCGCATCCCCAC	84182
rs191836532	snp	A/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30801799	GATTTCCCTTGACTC[A/T]GATTTCCTTTGAGAT	84182
rs191839746	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30824229	AGTGCTGAGGTAGCT[C/T]AAGGCATCACATGAT	84182
rs191868933	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30890103	ATCACCAAATGACAC[A/G]GAGGAGGACGCAGAG	84182
rs191872393	snp	C/G	0.0023933	0.0345097	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30855121	CAGAGGAGGCCTGGA[C/G]CAGGGGCCTGGGGGC	84182
rs191974189	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30787606	GTGTAGCCTTGCCTA[A/G]TAGCTCCAGACAGCA	84182
rs191994683	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30819795	TGATAGCATTTAGCT[A/G]CATCACCTTTTAAAT	84182
rs191999766	snp	C/G	0.021333	0.101051	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30820118	GTTTTAGCCGGGATG[C/G]TCTTGATCTCCTGAC	84182
rs192015831	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30886649	GTGGGCAGTGACTTC[A/C]CACCACCTGGCTTTG	84182
rs192018394	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30776962	TTGTCCTCTACCCCA[A/G]TGGTATTTCTTTTCT	84182
rs192020627	snp	A/G	0.00398564	0.0444627	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852923	ATGTTTTCTCTTGAA[A/G]TGTTTTTTCCTGGCC	84182
rs192061010	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30891595	AGGTGCCTCTAAAGT[A/G]CCAACCATTGGGTCC	84182
rs192075065	snp	A/G	0.0023933	0.0345097	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30857785	ACAGCCTTAGCCAGG[A/G]GCATCCTCTTGGCAC	84182
rs192078132	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875437	CCCCAGTCTCCTCTC[C/T]ACTCTTTCAGTAACT	84182
rs192114442	snp	C/T	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30809943	AGCCCTTTGGGAGGC[C/T]GAGGTGGGTGGATCA	84182
rs192135093	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30842493	GATACTGAGCACATA[C/T]GCACCTACCTACCTA	84182
rs192143940	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840482	CCTATGGTGATGTCC[C/T]TGGCTTCACAGCTGA	84182
rs192151018	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30783138	GGCAAGGTGTTAGCA[A/G]GCCTGGTTCTGTCTG	84182
rs192154543	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30827165	GATGCAGGATGTTGG[A/T]GAGATGTCTTTGCTG	84182
rs192160377	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872982	TCTGGCTCTCAGCAC[A/G]TGGGGGGCCACAATG	84182
rs192184970	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30816547	GTGTTCTCTGCAGCC[A/G]AACAGCCTGGGCCCG	84182
rs192220835	snp	C/G	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859593	GGAGCTTGCCTGGAA[C/G]TGCAGTGCATGCACA	84182
rs192231523	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30880057	AGCTCCATAAGGACA[A/G]CACTGTTCTTATTGT	84182
rs192233577	snp	A/G	0.00557542	0.0525036	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30878652	CAGGAGGGATGGGGT[A/G]GGACAGGGAGTTTAG	84182
rs192262888	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30770585	TCTTGGTCTGTAGCC[C/T]TCAGAACTGGGAGAC	84182
rs192270090	snp	A/G	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30821578	TATTTTTACATGTCC[A/G]TTTGAATCTCATGTT	84182
rs192291407	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30789780	TCAGAATTTTAAACC[A/G]AGGAAAAGCCTGGTA	84182
rs192293557	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30846865	CATGCACAATTCACA[A/G]TAGGGTTCCTGCCCC	84182
rs192294949	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30807055	CCTTTCTTCTTTAAA[C/T]AAAATTTCTTTTGAA	84182
rs192295283	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30790568	TCTGCTTCCACCTCC[C/T]GAGTAGCTGAGATTA	84182
rs192296194	snp	A/C	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853647	GGGTGAGGGATCTGG[A/C]TCCTGCCATTGCATC	84182
rs192298147	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30804528	ATCCCGACAAATATG[C/T]ACTACAGGATTAAGA	84182
rs192302114	snp	C/T	0.00120024	0.0244679	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30830642	TAGCATGAGGGTAAC[C/T]GCCCCCATGATTCAA	84182
rs192302291	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30813420	GAAAGTTTCAGTACA[A/G]CCTTTCCACCGTTGA	84182
rs192332812	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30867244	CTGTATCCAAATCCT[C/T]TTCAGATATTCACAG	84182
rs192344083	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30851605	CTTCCAGTTAACTTA[A/T]TAACCCCGGCCCTTA	84182
rs192360510	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30826488	GATGGAATGAGCAGC[C/T]TATGAAAAGATATAG	84182
rs192396609	snp	C/T	0.016272	0.0887199	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875685	CACGTTCACCACAAG[C/T]AGGGGAGCCTGACTC	84182
rs192417165	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30809771	CTTTGGAAAAGAATG[C/G]TTATCATCTTCGAAA	84182
rs192433925	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30794693	AGATGCTTGGAAAAT[A/G]TGTCACCTGGACTCC	84182
rs192439770	snp	C/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30774748	AGACTGTCCCTCTTA[C/G]CTTTCCTCCTACTCC	84182
rs192500974	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30773919	ATAATTGCACCCTCC[A/G]TAACAGGTGCAGCTC	84182
rs192526568	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30831672	GTTTCTGGTGTTGGG[A/G]CACTTCCAGAAGATA	84182
rs192567109	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30860533	CATTTCTGGGCTGAC[A/G]GGTTGGGTGGGAGTC	84182
rs192601145	snp	A/C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30799331	CAGGGTCCTGTGACT[A/C/T]TGGAGTCCTTCCTAG	84182
rs192669022	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30884384	TGGTGCTTCTTTCGT[C/T]GGGAGGATTAAGGGC	84182
rs192694091	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30806748	TTTTTTTATTGAAGG[C/T]TAGGGGAAGGTGGGT	84182
rs192709047	snp	A/G	0.00636936	0.0560724	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30838381	TCAAGCAGAGTTCAC[A/G]GGGGACCACTCATGG	84182
rs192819261	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30847659	TTTGATGAAATAACA[G/T]GGAAAGAGTTTATAA	84182
rs192821418	snp	C/T	0.00318978	0.0398085	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30813704	CAGGGTGTACTTGTC[C/T]GAACTGGGGCTGGCT	84182
rs192828875	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30879301	CACACAGCAGGAAGT[C/G]CTTCTGAAGGTACGG	84182
rs192856536	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778735	TGGGTTTTCCATCTC[A/G]GTCAGCTGGTGCCGC	84182
rs192881831	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30795813	TGGCTCCCTTCCTTC[A/G]CCTTTGAAGCCAGTG	84182
rs192885993	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30817062	TAATTTGAAAAATGC[A/G]TGTGAATATCCAGTG	84182
rs192894348	snp	C/G	0.00874735	0.0655527	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30883789	ATCCTGGTCCCTTCT[C/G]GGGGAGCAGTGGAAC	84182
rs192898536	snp	A/G	0.00874735	0.0655527	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850052	TTGGAGGTGGGCATG[A/G]CCAGGGCCAGGGCAG	84182
rs192938084	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30838458	GACCAGGAGTTGGCA[A/G]GTGTTTTCTGTAAAG	84182
rs192946956	snp	A/T	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30870741	TTAAAGCATACATTG[A/T]GACCAAGTTTATCTT	84182
rs192961619	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778198	CAGGACTCCTGTGCG[C/G]GAGTCCTGAACTCAC	84182
rs193007425	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30857100	TCCTACTTCCAAAAA[A/G]AGACTGGAAGTTGCT	84182
rs193010655	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30802735	ACTCAGTAATTTTTT[C/T]GTTCATACAAAACTA	84182
rs193014498	snp	C/G	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30890994	CCCCTTTTTCTTCCT[C/G]CATGGCAGTTAGATT	84182
rs193022024	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30835070	TCACTTCCACATTTT[C/T]GGATATCTTTTCAGC	84182
rs193084866	snp	A/C	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30834356	TGCACCTTTGAAGCC[A/C]CAGCCTGAGCTGTAC	84182
rs193098965	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30775043	CTCAACATGTCTCTG[A/G]TAGTGTTTCTGCTCA	84182
rs193106559	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30801985	CTGAGTCCTGGGATA[C/T]AGGCTGGGAAGATGT	84182
rs193154566	snp	C/T	0.00318978	0.0398085	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30864568	GAAGGTCCTTCTGCA[C/T]GGTGGGCTCAAGGGA	84182
rs193168003	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30854052	TGGCCAGGGCCAGAC[A/G]GCAGCAGATCACAGG	84182
rs193171933	snp	A/G	0.0023933	0.0345097	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30821776	TCTCTCCTGATGGTG[A/G]TATTCTGAGTAATGT	84182
rs193178854	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30888659	AATCGGGGAACGATT[C/T]GATTCGTCCCCTACA	84182
rs193182182	snp	C/T	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30798740	CTTGACCTTGTGATC[C/T]GCCCGCCTCGGCCTC	84182
rs193207079	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30818605	GTGTCAGTGAGATTC[A/G]TAGCTGGGATGGGTG	84182
rs193209016	snp	A/G	0.00398564	0.0444627	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30841997	GACACTGTTCACTAG[A/G]AGAGCCATCCAGCCA	84182
rs193209751	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30784918	CCATTTATGGCAGAG[C/T]CCAGTGGTAGAAAAT	84182
rs193215000	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875059	CAGTCATGTGGCCTC[A/G]TGTTCATCTGGCTCC	84182
rs193260625	snp	C/T	0.0023933	0.0345097	upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30770218	CGGGAGGTGGTTGTT[C/T]ACTTGGCAGTGAGCC	84182
rs199503923	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30833268	AATAGAGAACTCACA[A/G]TTCCACGTTGCTGGG	84182
rs199507615	snp	A/T	0.0189856	0.0955633	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30822626	TTGACGTGCCTGTCT[A/T]TTTTATTTATTTATT	84182
rs199507724	in-del	-/GA			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30812270	ATGTGTATGTGTGTT[-/GA]GGGGGGGGGGGTATG	84182
rs199523592	snp	C/T	0.000182169	0.00954208	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875583	GGGATGGGAACATCA[C/T]ACTTCTCAGAGGCAT	84182
rs199598520	in-del	-/ATC			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839658	GCCTTCTTAGGCTGA[-/ATC]TCATTGAGAGATTCA	84182
rs199649103	snp	A/G/T	0.000399284	0.014124	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882278	AGCCGGGGCTCCTGC[A/G/T]TGACTGGAGGACTGA	84182
rs199732745	snp	G/T	3.32011e-05	0.00407424	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859360	ACTCCCTGGGGCTGG[G/T]CTGGTCTGTCTTGTT	84182
rs199751467	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30807892	TCACTCGGGGAGCTC[A/G]GTTGTTGGAGATGTG	84182
rs199756930	in-del	-/AAAG			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30845534	AAAAAAAAAAAAAAA[-/AAAG]GGCAAGCTCTTCTGT	84182
rs199800554	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30833568	CTGCCCCTAGCCCCT[C/G]CCAAATCTCATGTCT	84182
rs199816608	snp	A/C/G/T	0.000298174	0.0122073	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791253	GGAAGGTCCCTGAGC[A/C/G/T]CTTTGTCTGCACCCA	84182
rs199859100	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30809793	TCTTCGAAAAAAAAA[A/G]GGGGGAAAAAAAAGG	84182
rs199886553	in-del	-/TCTT	0.0722614	0.17581	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30792748	TTTATGTTCTTTCTC[-/TCTT]AACTAGTCTCACTGG	84182
rs199941438	snp	C/G			missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782112	AAGAAAAATAACAAA[C/G]TGCCATCAAGATGCT	84182
rs199974230	snp	A/G	0.00021748	0.0104256	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839300	CCTCATTAAAATACG[A/G]CATAGTGCAGAACAA	84182
rs199975258	snp	A/G	0.000678802	0.0184103	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828683	CTATTTTCCAGGAAA[A/G]ATCAGTTGCTGCCGT	84182
rs199980276	in-del	-/AA			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30809561	GAAGGAAAAAAAAAA[-/AA]GCCATCTATACAATT	84182
rs199982387	snp	C/T	1.66726e-05	0.00288722	stop-gained, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840847	AAAGCCGACTGTGCT[C/T]AGTAAGTCAGTGCTC	84182
rs199983607	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30868501	GCTCAGTGGCAGAGC[C/T]TCTTCCCCTTCCGGG	84182
rs199983860	in-del	-/TG	0.104149	0.203046	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30847707	TAAATACTCTATATA[-/TG]TGTGTGTGTTTTTTG	84182
rs199994000	snp	A/T	0.217551	0.247885	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30858658	TGTTTTAAAAATATA[A/T]ATATATATATATAAA	84182
rs200053449	snp	A/G	0.00886995	0.0660023	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778512	CAGAAATGATCTTCG[A/G]AAGGTTTTGCATCTT	84182
rs200088510	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30789408	AGATTCTCTAGAAGG[G/T]ACATTGTGGCCTTTG	84182
rs200111157	snp	A/G	0.00259484	0.0359261	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882350	AGCAGGAGCAGATCC[A/G]GCTGACCATTGGTGC	84182
rs200117017	snp	C/T	0.000811345	0.020125	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828731	GAGCTGGGTGCCCTG[C/T]GGCTCGGTAGGTGCA	84182
rs200146980	in-del	-/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30777014	TTCTTTTTTTTTTTT[-/T]AGAGATAGGGTCTCA	84182
rs200165290	in-del	-/T	0.454544	0.143743	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30858656	GATGTTTTAAAAATA[-/T]ATATATATATATATA	84182
rs200170955	in-del	-/GG			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30843605	GTTACCCCACCCCCA[-/GG]CCACATCCATGGGGT	84182
rs200190105	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30784707	CTCTCAGACTCAGGT[C/G]CTGCCTTCTCTGGGA	84182
rs200192134	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30838056	ACAGGGAAGTGGCTG[G/T]AGAATCCACCTGCTG	84182
rs200221932	snp	C/T	0.000604453	0.0173741	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791192	AGACACTATCTGAGA[C/T]GGTCCTCACCGTCAA	84182
rs200226382	snp	A/G/T	9.93582e-05	0.00704771	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875528	CTGACTGGGAAAGCT[A/G/T]TGTCCAACGTTTTCA	84182
rs200254192	snp	A/C	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30833387	AGCTTCTGTTTTTAA[A/C]AGCCATCATATGTCA	84182
rs200350953	in-del	-/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30777018	TTTTCTTTTTCTTTT[-/C]TTTTTTTTAGAGATA	84182
rs200411106	snp	C/T	7.67902e-05	0.0061959	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853389	GAGTGTTTGTGTCTT[C/T]TCAGCTTACGCTTCA	84182
rs200421570	snp	A/G	6.62383e-05	0.00575454	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875544	TGTCCAACGTTTTCA[A/G]CGATGTGGTTGAGCT	84182
rs200422890	snp	A/G	0.000133229	0.00816068	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791203	GAGACGGTCCTCACC[A/G]TCAAGCAGCTCCACC	84182
rs200443455	in-del	-/TTCT			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30877681	TTCTTCTTCTTCTTC[-/TTCT]TTTTTTTTTTTTTTT	84182
rs200483058	in-del	-/GAGA			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30808933	AAAGAGGGAGTCAAG[-/GAGA]GAGAGAGAGAGAGAG	84182
rs200489033	in-del	-/GT	0.00835141	0.0640778	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30829915	AAGCAGCTGTTTGAA[-/GT]GTGTGTGTGTGCATG	84182
rs200494217	in-del	-/TTTCT			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30822175	TTCTTTCTTTCTTTC[-/TTTCT]TTTTTTTTTTTCTTT	84182
rs200500128	in-del	-/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30824982	CTCATGCCTCTCTCT[-/G]GGGGGGCATGAGAGG	84182
rs200532146	in-del	-/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872863	TTTCAAGATGTTACC[-/T]AGTGAGCATCAAAAC	84182
rs200534896	in-del	-/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30879943	TTAGTGATACAAAAA[-/T]ATAATGGCGAATCTG	84182
rs200537877	snp	A/G			upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30770297	CTCAAAAAAAAAAAA[A/G]AAAAAAGAAAAAAAA	84182
rs200549607	in-del	-/TTTC	0.230379	0.249229	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30822159	ACAGTACCCACAAAA[-/TTTC]TTTCTTTCTTTCTTT	84182
rs200594752	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30871506	ACGTGTGGCACACCT[C/T]TGCTCACCGGGATAC	84182
rs200610055	snp	A/C/G	0.000156918	0.0088565	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872344	AGGTGGTCCTTCCCC[A/C/G]TCCTCTGTCCCTCAG	84182
rs200628042	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30786735	AGTTTCATTTATTCT[G/T]CTTTTATTTTTTTCT	84182
rs200634054	snp	C/T	0.00199792	0.0315431	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836750	TCAAAACCAATTGAC[C/T]TCTCAGTAGCAAAGG	84182
rs200700624	in-del	-/T	0.0482946	0.147699	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30858097	GAACACTGACTATTA[-/T]TAACAGGCGGTGTCT	84182
rs200739747	snp	A/G	4.97006e-05	0.00498476	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852284	TCTTAGAAACAGTAC[A/G]ACTTTCTGGAAAATT	84182
rs200781616	in-del	-/TTTTTGTTTA			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30793155	ATATATATTGTTTAT[-/TTTTTGTTTA]TTAATTGTTTATATA	84182
rs200785914	snp	A/C	0.0004824	0.0155231	utr-variant-5-prime, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771475	CGTGGGCCTCGTGGG[A/C]AGAGCCAGAGCCAGA	84182
rs200838576	in-del	-/A	0.0154538	0.0865337	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30820602	ATAATATATAAACTT[-/A]CGGTGTCAGGCTTCT	84182
rs200843454	in-del	-/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30822627	TGACGTGCCTGTCTA[-/T]TTTATTTATTTATTT	84182
rs200855134	snp	C/T	0.00112745	0.0237161	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778383	GCTTTATGAGAACAG[C/T]GGGTTTTGATTTAAG	84182
rs200911726	in-del	-/TG			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839655	GGGGCCTTCTTAGGC[-/TG]TGATCATTGAGAGAT	84182
rs200913656	snp	C/T	9.94481e-05	0.00705083	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882955	TGAGGACACAGACAA[C/T]GACCTTGTCCCACCC	84182
rs200916352	snp	A/G	0.000765467	0.0195486	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839284	TCCTTTAGTAACACA[A/G]CCTCATTAAAATACG	84182
rs200938852	snp	A/G	0.000933937	0.0215893	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791547	AAAGAGCGTTCAAAC[A/G]GCAGGGCAGCCAGCC	84182
rs200977322	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30863969	CTGGGGTCAGGACAG[A/C]TCTGAACCAGACCTG	84182
rs200980067	in-del	-/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30847716	TATATATGTGTGTGT[-/G]TTTTTTGTTGTTTGT	84182
rs201070084	snp	G/T	1.90282e-05	0.00308444	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882345	CAACCAGCAGGAGCA[G/T]ATCCGGCTGACCATT	84182
rs201112733	in-del	-/T	0.0162398	0.0886349	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30842620	TCATGGCACCTATGA[-/T]TGAACAGGAGAGCCA	84182
rs201132185	snp	A/T	0.109461	0.206758	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30841637	AATTGGCCTTTTTTA[A/T]AAAAAAAAAATTTAG	84182
rs201132541	snp	A/G	1.65652e-05	0.0028779	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852217	CCTTTCCTTTTTAGG[A/G]CTTCGAGAACACAGC	84182
rs201164640	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30833490	TCCTTCCCACAACAT[A/G]TGGGAATTATGGGAG	84182
rs201174256	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782338	AGTCTCTGTGTGTGT[A/G]TGTTTGTGTGTGTGT	84182
rs201255432	in-del	-/TTC			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30822176	TCTTTCTTTCTTTCT[-/TTC]TTTTTTTTTTTTCTT	84182
rs201284950	snp	A/C	6.62767e-05	0.00575621	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782085	ACCCCAATCCCTGCA[A/C]TCTCAGTTCCAAAGA	84182
rs201320237	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839146	ATGCACACTGAACAT[C/T]GTATTGTTGCTTGCT	84182
rs201332783	snp	A/G	0.00158935	0.0281451	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852189	CTCTCCACTCAGAGG[A/G]CTCATGCACCTTCCT	84182
rs201335083	snp	C/G	0.000149371	0.0086408	stop-gained, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836754	AACCAATTGACCTCT[C/G]AGTAGCAAAGGTAAG	84182
rs201348400	snp	A/T	0.00038112	0.0137991	stop-gained, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791351	ACCGTAGAAAGGCAG[A/T]AAACCACTGCCAGCA	84182
rs201362298	snp	A/G	4.98418e-05	0.00499183	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839243	GCTTTTGCTGTTTCA[A/G]TGAAGAATGGAAACT	84182
rs201386276	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30811971	TTTTGTCTGTGGCTT[A/C]TCCTGCTACAGTCCA	84182
rs201392222	snp	A/G	0.00199799	0.0315437	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778373	GTTTGCTTGTGCTTT[A/G]TGAGAACAGCGGGTT	84182
rs201431961	snp	A/C/G/T	6.7879e-05	0.00582546	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872232	CTAACAATGCTTCTT[A/C/G/T]TGTTTTCCAGCATCC	84182
rs201463682	snp	C/T	1.67144e-05	0.00289084	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791197	CTATCTGAGACGGTC[C/T]TCACCGTCAAGCAGC	84182
rs201465190	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30777014	TTTCTTTTTCTTTTT[C/T]TTTTTTTTTTTTAGA	84182
rs201466750	snp	C/T	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30821722	TTAGAAGTTTTTCCT[C/T]CATTTCTCTTATTTA	84182
rs201479938	in-del	-/TATA			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30793165	GTTTATTTAATTGTT[-/TATA]TATGTATTATTCTTT	84182
rs201525972	snp	A/G	0.499017	0.0221427	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30786630	ACCCTGTCTCAAAAA[A/G]AAAAAAAAAAAAAAA	84182
rs201541108	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853055	GCCCCTGCCTTATCC[A/C]CCTCCCTGCCAGCCG	84182
rs201582796	snp	A/G	1.65625e-05	0.00287766	utr-variant-3-prime, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30892008	CCCCATCCTGTGACC[A/G]TTGGATGTGGGTAAA	84182
rs201645679	snp	C/T	0.000976878	0.0220791	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828736	GGGTGCCCTGCGGCT[C/T]GGTAGGTGCAGCGGG	84182
rs201662405	snp	C/T	0.000129298	0.00803942	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791120	ATCTTTGTTTTCCAG[C/T]TCCCCTCAAAGGGTC	84182
rs201694248	snp	A/G	3.31565e-05	0.0040715	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875607	GAGGCATTGCTGCAC[A/G]CAGTGATATTGGCTT	84182
rs201694842	snp	C/T	0.000353312	0.0132865	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872247	GTGTTTTCCAGCATC[C/T]GCCAGGACTTTGATG	84182
rs201750903	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30857329	AGTCTGTGTTGAAGG[C/T]CCTTCCTGTGTGTTT	84182
rs201777506	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30780061	GAGGAGAAGTAGGCA[A/G]TGGCAGCCCCGTGAA	84182
rs201826714	snp	A/G	0.00199792	0.0315431	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839359	CCTTTCTGCTGGGCC[A/G]TCATGCATAGGGGTG	84182
rs201907604	snp	C/T	0.000283086	0.0118938	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850479	CCTTCAGATGCCCAC[C/T]GGACCCGCTGCCTCG	84182
rs201918244	snp	A/G	0.000132542	0.00813964	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875597	ACACTTCTCAGAGGC[A/G]TTGCTGCACGCAGTG	84182
rs201934512	in-del	-/TAC			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30847540	ATTTTTTCCAGTTTT[-/TAC]TAACTATCTGATCTG	84182
rs201946407	snp	G/T	0.0088701	0.0660028	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778526	GAAAGGTTTTGCATC[G/T]TGAATTTCTCTATAA	84182
rs202006369	snp	C/G	0.000517598	0.0160789	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791593	AGTGTGCTATGCAAA[C/G]GTGACGGCTTTTCAA	84182
rs202097064	in-del	-/C	0.0360663	0.129354	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30880247	ATTGTGCTACATGTT[-/C]CCCCACCAGGACAAA	84182
rs202118398	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30796124	TGGAGCACTGTACTT[A/T]TTTTTTTTTTGTCTC	84182
rs202120302	in-del	-/A	0.109461	0.206758	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30841636	CAATTGGCCTTTTTT[-/A]AAAAAAAAAAATTTA	84182
rs202149651	snp	A/G	9.01429e-05	0.00671292	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859113	AGGAGGTCAGCCTTC[A/G]GGCCACCCAGCAACC	84182
rs202153982	snp	A/C/T	0.00142093	0.026617	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840891	CTTATTTTCCCAAGT[A/C/T]TTCCCCAGAGTGTCC	84182
rs202164342	snp	C/T	0.0022834	0.0337118	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791302	GAGCAACAGCTCCCC[C/T]TCCAGGACCTCCCTG	84182
rs207467755	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30844979	TACAGATGGGGAAAC[A/T]GAGGCCCAGAGAGGG	84182
rs367570978	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30815438	TGGGCCAGGCACCCC[A/C]TCACATCTCTAGCAC	84182
rs367574571	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30831037	AGATACCTAGGGCTG[C/T]GCATTTGGGGGCTAT	84182
rs367583446	snp	A/G	3.31664e-05	0.00407211	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791408	CTGCCCCCATGGGAC[A/G]GGGCCAGGCCGAGGG	84182
rs367591607	snp	A/C	0.00023287	0.010788	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853503	TGTGCGTCACTAAGC[A/C]TTCTGATTTCACTGT	84182
rs367602579	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30887158	CTCCCTGCGGAACCT[C/G]CCGTTCAGCTTCCAT	84182
rs367604835	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30822833	TTTTTTTGCAGGGAT[A/G]GGGTATCACTATGTT	84182
rs367622721	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30838666	AGTTTAGTAACCCTG[C/G]ACTAGAGCACTGGCT	84182
rs367630119	in-del	-/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30866161	GCTGAGAAGGGGGGC[-/C]ACACCCAGGCCACTG	84182
rs367638325	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30795738	GCATTCCTTCTGGAG[C/G]CTCTAGGGGAGAATC	84182
rs367639823	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30830337	AAGCAGATGCCCAGC[A/T]GTGCTTAAGTGCTTT	84182
rs367643931	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30812550	GGAATCTGGGTGAGG[C/T]GATGGTATAAAACCC	84182
rs367707422	in-del	-/A			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30822621	TTGGTTGACGTGCCT[-/A]GTCTATTTTATTTAT	84182
rs367712233	snp	A/G	0.000175948	0.00937779	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850593	TTGCCGTGGCTCATC[A/G]TCTGCTGGCAGCTGC	84182
rs367757884	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853810	CTGAGTGGAAGCAGC[C/T]GCCACTGGAATACAG	84182
rs367758201	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828611	ATCCATCGCTCTTAA[C/T]AGTCTTCTCTGCCGT	84182
rs367782465	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30890286	TTGACTAGGGAGCAC[A/G]ACGTAGGGCAGGACT	84182
rs367849284	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30792649	TATTGGTATAAAATT[G/T]TATAATTATATTATC	84182
rs367858687	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30848605	CTGAAACCTAGAGCA[A/G]TGTTTTCTCATGGTG	84182
rs367901408	snp	C/G	1.65754e-05	0.00287879	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882950	ATCTCTGAGGACACA[C/G]ACAACGACCTTGTCC	84182
rs367941864	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30776545	TCCCCCTATAGAGTG[A/C]AAGCTCCCTGAGGAC	84182
rs367978512	snp	C/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30865812	CAGTTGGCAGCATCA[C/G]CTGAGGCTCCTGGCT	84182
rs367992526	snp	C/G/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30834935	GTTCATACTACTATC[C/G/T]GCATTTTTGTCAAAG	84182
rs368012824	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30800985	ACATTCACCAGGCCC[A/T]ACCAGACCTTTCTTA	84182
rs368014003	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30804662	TGACTGGCCCTCTTA[C/T]AGGAGCTTTGGATGT	84182
rs368023962	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872863	TTTCAAGATGTTACC[C/T]AGTGAGCATCAAAAC	84182
rs368051174	snp	C/T	0.000199025	0.0099736	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791452	CACCCCAGCAGTGGA[C/T]GGCAGCACAGACACG	84182
rs368080184	in-del	-/TG			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30829926	TGAAGTGTGTGTGTG[-/TG]CATGTTTTCTGGAGG	84182
rs368084111	snp	C/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30825925	AAGGTGTTGAAAGGG[C/G]TGGTTGTTTCTTGAG	84182
rs368105372	snp	C/T	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30792145	ATTTTATTTTTCATC[C/T]TATCCTTACTTTTAT	84182
rs368109120	snp	C/G	0.000437904	0.0147905	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828800	GTCCTCGTTGGCTCT[C/G]TCTGGGAGATGGGTG	84182
rs368114540	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30848280	CCCCCACCCCCACCC[C/G]ATGTGTATGTGCAAT	84182
rs368120864	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30841148	CTGCCCGAATCCCTT[C/G]CACCCACCAGGTCGA	84182
rs368150973	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30812277	TGTGTGTTGAGGGGG[C/G]GGGGGTATGTATGTA	84182
rs368182062	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30827128	AGAGAGCAGAGGTGG[A/G]GGTTCAAGAGAGATG	84182
rs368190972	in-del	-/TCT			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771963	CACTCGGAAAGAACT[-/TCT]CCCAGAGGGAACCCC	84182
rs368218709	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30891134	TGTAGAACTGCTGTG[A/G]GATATTCAACATCTG	84182
rs368258148	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30849058	GGGGCCACTGTGTTC[C/T]GTCACCTTTTAAAGT	84182
rs368277365	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30833675	CACAGTTTAAAGTCT[C/T]ATTTGAGACAAGGCA	84182
rs368287412	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30865588	TGTAGATCTCTGCCT[C/T]GCTTCCTCTGGAGAC	84182
rs368335229	snp	A/G	0.000159987	0.00894248	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791501	CTCTACTTGCCTGGT[A/G]GTAATTCCAGGATGA	84182
rs368338029	snp	A/C	1.7285e-05	0.00293977	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872210	ACCTGGGTCAGGCAG[A/C]GCTGTGCTAACAATG	84182
rs368350379	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30847716	TATATATGTGTGTGT[G/T]TTTTTTGTTGTTTGT	84182
rs368352590	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30860475	TGGAGACCATAAGCT[A/G]CACCACCTTCTCCCC	84182
rs368362730	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30869698	TTTAAGTTAGTCACC[C/T]CTTGAAAGGCTCTAT	84182
rs368365866	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30887062	CGGAGGTGCAGACAA[C/G]AAATTGAAAATGTAA	84182
rs368368484	snp	A/C/T	0.000376807	0.0137218	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882381	GGGCCCTCACCCCCC[A/C/T]ACCCACCCAACCCTG	84182
rs368374263	snp	G/T	0.000163986	0.00905352	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778527	AAAGGTTTTGCATCT[G/T]GAATTTCTCTATAAG	84182
rs368385065	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30838415	GCATCACAGAGGAGG[C/T]TCTTACGCATGGTAG	84182
rs368403761	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30823790	GTGTTTAAGAGTTTT[G/T]TGTTTTGAGCATATT	84182
rs368497079	snp	C/G/T	5.00624e-05	0.00500291	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840718	CCAAAAACTCTGCCC[C/G/T]AGGCCAGTTCTCACT	84182
rs368538211	in-del	-/TT	0.0799831	0.183287	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30851999	TCTTTTTTCCATTTC[-/TT]TTTTTTTTTTCTTTT	84182
rs368571242	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30821251	ATCTAAATGCTTGCC[A/G]ATTTCTTTTCTTCCT	84182
rs368583511	snp	G/T			upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771089	AGGGTGGACCTGAGG[G/T]GGTCACTTCCCTGTG	84182
rs368593149	snp	A/G	0.0103295	0.0711199	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30789168	ACTACTCTGAGGACC[A/G]GTGAACCAGAGAGGA	84182
rs368619585	snp	C/G	3.35801e-05	0.00409743	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850554	AGAGCCGTTGTTGCA[C/G]TGTAAGTGGTTCCGA	84182
rs368622145	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30878215	CCATGACGTCCGCAG[C/T]GTTCACTCACTAGCA	84182
rs368625851	snp	C/T	0.000115928	0.00761251	utr-variant-3-prime, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30892009	CCCATCCTGTGACCG[C/T]TGGATGTGGGTAAAC	84182
rs368634456	snp	C/T	0.000159987	0.00894249	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836649	CACATGGCCATGGTT[C/T]TCTTTCAGAGGATGT	84182
rs368653636	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30861376	GAGTCCACAGCAGCC[C/T]TGTTAGGTGGGTGCT	84182
rs368674299	snp	A/G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30804020	CCTGCTGGAGTACTG[A/G/T]GTGTATGCCTTCCCT	84182
rs368682080	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30879252	ATCCAGTATGGCTGG[G/T]ATCCTCCTAAGCAGA	84182
rs368690951	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30830825	GTCTTGTCAAATAGC[A/G]ATGTGGAAGGAGCCA	84182
rs368711343	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30814382	TCTTATTTCAAGATT[A/T]TGTCAACCTTTAGAA	84182
rs368725280	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30784162	AAGGGGCTATGAAGA[A/T]GCTCTTCCTCCGAGG	84182
rs368760286	snp	C/T	0.000167986	0.00916322	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782017	GCCTTGAACTCATCA[C/T]CAGATACTTTCTGGA	84182
rs368777512	snp	A/G/T	6.63563e-05	0.00575972	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840760	TCTCATTCTTTGCAG[A/G/T]GTGGTCCTTGCGGAG	84182
rs368782018	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30772577	GCACGTAGGTGTTCA[A/G]CTTTATACCTCCTCC	84182
rs368816516	in-del	-/TC			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30776993	TTTCTTTCCTTTTCT[-/TC]TTTCTTTCTTTTTCT	84182
rs368872136	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30813344	GTGTTAAAGTGTTCA[A/G]TCCCCAGGTCCTGAA	84182
rs368888758	snp	C/T			utr-variant-3-prime, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30892144	AGCATCCAGAGCCTC[C/T]CTGCCCCTTCCATGA	84182
rs368931883	snp	C/T	0.000155988	0.00883004	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882910	GTGTGTGCCTCTCTC[C/T]TCCTTCCCAGACACC	84182
rs368933809	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30846584	GGCGTGCGCTGAGCT[A/C]TCTGGTAAAGGCCTG	84182
rs368959222	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30878778	AAGCTCCATCCTCCT[A/C]CCATCCTCCCCAGCT	84182
rs368974185	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30813604	GGTTTGCTACCCAAG[C/G]ACCCTCACAACCCAT	84182
rs368978423	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30829941	GCATGTTTTCTGGAG[A/G]GAGGCCGACCCCTCT	84182
rs368978485	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30861011	CACACAGAGACACAC[A/G]CACACAGACACACGA	84182
rs368986863	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30809253	ACCTGCAGTAACCTG[C/T]GGATGGCCCAAATGC	84182
rs368993136	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778892	GTACTTAAGAATATC[G/T]TATCCAGTTATACTA	84182
rs369008240	snp	C/G	3.02384e-05	0.00388823	utr-variant-5-prime, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771487	GGGCAGAGCCAGAGC[C/G]AGAGCCATGGACAGC	84182
rs369033084	snp	C/T	0.00398564	0.0444627	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30821286	TGAGTCCTTGATCGT[C/T]CATTCAGTGAAGGTC	84182
rs369052821	multinucleotide-polymorphism	CG/TT			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30868200	GGCTAGGGGTAGGGC[CG/TT]TGGGACTCTAGGGCT	84182
rs369055721	snp	C/T	1.77786e-05	0.00298144	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882140	GCCCGGACCCCTTTC[C/T]CTGGGGACGGCATTT	84182
rs369084345	snp	A/G	0.157311	0.232183	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30819941	GAGTCTCGCTCTGTC[A/G]CCCAGGCTGGAGTGC	84182
rs369178286	snp	A/T	0.00517822	0.0506191	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30885352	TGGAGACACCCCATC[A/T]CTATTAAAAATTAGC	84182
rs369196289	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30835347	GACTTATTCACTATC[A/G]TGAGAACGGCACAGG	84182
rs369200214	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30806140	ATTTATTCCAATTAA[A/G]CAAAGCTTTGTTCAG	84182
rs369209973	snp	A/G	1.68026e-05	0.00289845	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782164	TATATGACCTTTCAG[A/G]TGAAGATGCAGGATG	84182
rs369212440	snp	C/T	1.65669e-05	0.00287805	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836708	ATCCTGTCGCCAGTC[C/T]CATCAGTGCTCAAGT	84182
rs369232784	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30866203	GGTCTCAAGACCCTC[A/G]GTCCTGTGTGCATCT	84182
rs369262711	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30891554	TGTCCCCATTGTTTC[G/T]CACTCAGCCATATCT	84182
rs369281298	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30801530	CACTTCTCAGCCTGT[G/T]GATCACATTTTACCC	84182
rs369324934	snp	A/C	3.13583e-05	0.00395957	missense, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771548	GTCAGGGAGTTCCTC[A/C]GCAGAAAGGTAACGG	84182
rs369369905	snp	G/T	0.00523164	0.0508768	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882164	GGCATTTCACATCAG[G/T]CCTCTCCCTCATCCA	84182
rs369376987	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30829317	CTGTAATTCCCTACT[A/C]TCCAAAGACATGCAT	84182
rs369416134	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30820032	TCAGCCTCCCAAGTA[G/T]CTGGGACTACAGGCG	84182
rs369432501	snp	A/G/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30842678	TGCACGGTGCTAAGG[A/G/T]TTCATCTGGACATGA	84182
rs369462193	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30883054	TTGAGGAGCCATGGT[C/T]GGGGGTGGTCAGGCC	84182
rs369492014	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30870306	TGCTTATCGGCCCCC[C/G]CTCAGGACCCTTTTG	84182
rs369500000	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30809298	GGCAACTGCTTAGCT[A/G]ACAGAAAAAATTTAA	84182
rs369542262	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30889893	TTTATTCTTGAAATA[C/T]CTTTTAAAAATGTAT	84182
rs369560432	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30813224	TGTAGAAGATTCATC[A/G]TCAGGAGAAAAGGGA	84182
rs369570807	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30861295	ATTGCCAGCGGTAAG[A/G]ATAGCGTCTGTGAAG	84182
rs369576794	snp	C/G/T	0.000140268	0.00837363	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791622	AAAAAGAAGCTCCAC[C/G/T]TCTCACATGTTGTCT	84182
rs369620192	snp	C/G/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30871210	TCTCACGTTGCCCCC[C/G/T]AGAGCCAGCTTCTCT	84182
rs369629656	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30824837	AATGCTGGGACTATA[A/G]GCATGAGCCACCACA	84182
rs369634946	in-del	-/A			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30889193	AATCTTAATAGAACA[-/A]TAAAAGCTTTTTAAT	84182
rs369651501	snp	C/T	6.63119e-05	0.00575774	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882969	ACGACCTTGTCCCAC[C/T]CCTCGAGCTCTGCAT	84182
rs369654882	snp	A/G	4.97632e-05	0.0049879	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785757	TTCACAGACATGACA[A/G]TCTTGATGGAGATGT	84182
rs369674215	in-del	-/T	0.454544	0.143743	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30858654	TTGATGTTTTAAAAA[-/T]ATATATATATATATA	84182
rs369701153	snp	A/C	3.31647e-05	0.00407201	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791389	CCATCTGCCCAGCAA[A/C]CGGCTGCCCCCATGG	84182
rs369717235	in-del	-/CGT			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30831981	TCCTGGCCAACATGT[-/CGT]TCTGGAGTGTTTTGT	84182
rs369733011	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30886692	CATTGCACAAGCCCA[A/G]ACTGCTGGTTTCGCC	84182
rs369790237	snp	C/T	1.65638e-05	0.00287778	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852264	GAAATACAAAGCAGA[C/T]GGAGTCTTAGAAACA	84182
rs369855457	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30805611	AGGAGGTTGCATTTT[C/T]GGACCCTTAGGAGAG	84182
rs369871299	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30790323	CACCCATAAGCAAAA[A/C]ACATGACCATTTCAG	84182
rs369880517	snp	C/T	3.31395e-05	0.00407046	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791245	AGAGAGCCGGAAGGT[C/T]CCTGAGCTCTTTGTC	84182
rs369892410	snp	C/T	0.02016	0.0983543	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30879451	CCGTGGTATTTGTTA[C/T]GGCAGCCCGAGCAGA	84182
rs369901852	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30774341	TTCTCCATACCCCTG[A/G]TTAGGCCCACCCCTC	84182
rs369957988	snp	A/G	1.67733e-05	0.00289592	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882204	CTTCCTGAAGACCCC[A/G]AGGTTCCCCATCTGG	84182
rs369985769	in-del	-/GT			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30847716	TATATATGTGTGTGT[-/GT]TTTTTGTTGTTTGTT	84182
rs370007106	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30880750	ACTAAGGAATGAGCT[C/T]TGCAGTCCACTTCAA	84182
rs370010726	snp	C/T	0.0023933	0.0345097	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30864358	AAAGCCAACTGTGAG[C/T]GTTGGTTGGAAAGAC	84182
rs370015862	snp	C/T	0.000134305	0.00819356	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872277	GTCCCCACCAGCCAC[C/T]TGATTGGAGCACATG	84182
rs370023193	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30832793	GATTACAGGCATGAG[C/T]CACCGTGCCTGGCCC	84182
rs370031394	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30815949	TCCAGCATGGGATAG[A/G]TTAAAATAAACCAAG	84182
rs370104814	snp	C/G/T	8.6622e-05	0.00658062	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850485	GATGCCCACCGGACC[C/G/T]GCTGCCTCGTCCTGG	84182
rs370142157	snp	C/T	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30867729	TGGTCAAGGGTCAGT[C/T]TCTGAGAGTGGCAAG	84182
rs370149704	snp	C/T	0.000132681	0.00814389	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791431	GCCGAGGGATCCCTC[C/T]GAGGACACCCCAGCA	84182
rs370172815	snp	C/T	0.000135853	0.00824065	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791546	GAAAGAGCGTTCAAA[C/T]GGCAGGGCAGCCAGC	84182
rs370181920	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30787860	AAAATTATTGTGGAG[G/T]GCAAAGAGCTTTTGT	84182
rs370187246	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30774945	AATTCCCAAATGTCT[A/G]TCTCTAGCTGAGACC	84182
rs370199441	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30793159	TATATTGTTTATTTA[A/T]TTGTTTATATATGTA	84182
rs370217178	snp	A/G	4.99555e-05	0.00499752	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30883021	CCTCTCTGGCTTTGA[A/G]CCTCACCCTGAATAG	84182
rs370217930	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30873108	GGAAACCTACGTGGG[A/C]ACCATACAAGGCAAG	84182
rs370220161	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850108	AGCACTGCTGGCTGG[G/T]CCTCCCAGTCCCTGC	84182
rs370226877	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30887550	GAGCAGGCAGAGAGG[A/G]GAGTGCAAGGCAGGG	84182
rs370252331	snp	A/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30886146	AGCCCAAGCTCCTGA[A/T]AAGATGCAGCTGTGT	84182
rs370262463	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30819970	GCAGTGGCGGGATCT[C/T]GGCTCACTGCAAGCT	84182
rs370294601	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30788558	TCTCAAGCTCACGGT[A/G]GCAGATAGAAGTTTT	84182
rs370328348	snp	G/T	1.66679e-05	0.00288681	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859223	AGAGGGAGGTGCAAA[G/T]GGGATGGAGCTCATT	84182
rs370331696	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30877045	GATACCCCCAGCATG[C/T]CAAAAGCAGACTTCT	84182
rs370410998	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30855664	TGAGATGGAGCCTCC[C/G]CCTCAGCCTGTACCC	84182
rs370417052	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850856	CAGAGGAAGCCTCTG[A/G]CCCCTGCAGCCAGCT	84182
rs370421052	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836532	GGGGTGAATGAATGC[A/G]GGGAGGAACCCTCCT	84182
rs370429366	in-del	-/AG			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30862406	TCTGGCCTTCCAGAG[-/AG]TAGTCCCCAGAACAG	84182
rs370432818	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30780581	TATCTACTACATAAT[A/G]ATTTTGACATTCATT	84182
rs370449280	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30845885	GCCTCTCCTCAGTCG[C/G]GAAGGATGGAGCTGG	84182
rs370449748	snp	A/G	0.0023933	0.0345097	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30860567	AGATCTCCCTGAGGG[A/G]AAGCTGCACTCTCAG	84182
rs370451194	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30876345	ACTCCAGTATGACCT[C/T]GTCTTAACTAATTAT	84182
rs370476529	snp	C/T	4.96915e-05	0.0049843	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30891924	ACCCTGAAGCTTGAT[C/T]TCTCTTTGTCTCTCT	84182
rs370477429	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30868758	TTTGGTCCTTGCTGG[A/C]ATCCTGGGCAAAGCT	84182
rs370489567	snp	A/G	0.000121541	0.00779458	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850517	CCTCGCAGACATTGT[A/G]TGGCGGGCAGGGGGC	84182
rs370506233	snp	A/G			upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30770119	CCCCGTCTCTACTAA[A/G]AGTACAAATATTAGC	84182
rs370534660	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30883737	CCCAGAGGCCTCAGC[A/G]TGCATGAGAGGAGCA	84182
rs370549146	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30799368	GGCTCCTCTGAGCAC[C/T]TGTGGGTATATAGTA	84182
rs370632946	in-del	-/TC			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30877682	TCTTCTTCTTCTTCT[-/TC]TTTTTTTTTTTTTTT	84182
rs370635096	snp	C/T	2.03482e-05	0.00318962	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853364	GCGTGGGGCTTGGGC[C/T]ACTCATCCTGAGTGT	84182
rs370640480	in-del	-/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30866063	GCTGAGATGGCAAGT[-/C]CACAGCCACTGAGCT	84182
rs370655350	snp	A/G	8.27972e-05	0.00643364	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875537	AAAGCTGTGTCCAAC[A/G]TTTTCAACGATGTGG	84182
rs370666189	in-del	-/CCCCACTAAGGGGATGCGAGAGCTTCTATATCCCCCA			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30843604	GTTACCCCACCCCCA[lengthTooLong]GGCCACATCCATGGG	84182
rs370680867	snp	A/G	0.00557542	0.0525036	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30811223	GTTACATGTATTATA[A/G]TAACTTATACTATAA	84182
rs370693145	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30837799	CGTGGCCTCTGGAAA[G/T]CAGAGTCCAGGTTCC	84182
rs370704492	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30780199	AGTCCTGTGGAAAGA[C/G]TGGTGACCCAGGCAG	84182
rs370716237	in-del	-/AG/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30812271	TGTATGTGTGTTGAG[-/AG/G]GGGGGGGGGGTATGT	84182
rs370750309	snp	A/C/T	6.62431e-05	0.00575481	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30891952	TCTCCTCACTCTACG[A/C/T]TTAGGTGGAAGGGGG	84182
rs370755072	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30841033	TAAGGGGACTTGTGC[G/T]CGTTTGTTTCTGAAA	84182
rs370755966	snp	G/T	1.65603e-05	0.00287747	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785932	GGGAGAGAATTCCAG[G/T]CCAAAGTCTGGTCTG	84182
rs370780288	snp	A/G/T	0.000153947	0.00877234	splice-donor-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882362	TCCGGCTGACCATTG[A/G/T]TGCGGGCCCTCACCC	84182
rs370795861	snp	A/G	0.000163986	0.00905352	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839330	AGGCAGGTTGCTCCT[A/G]GGTTTCCTTGGGACC	84182
rs370817972	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30838158	TCATGAGGGGAGTGG[A/G]CGGGGACCTGCTGCC	84182
rs370822049	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875934	GGTCACAGTGGCTGC[A/G]GCTGGTGTCTGTGTG	84182
rs370830723	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30832687	GCTAATTTTTGTATT[C/T]TTAGTAGAGATGGGG	84182
rs370832773	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30851770	CCCAAACCCGGCTCC[A/G]ATTCCTGGACGTCTT	84182
rs370833399	snp	C/T	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30783851	GGCAACAGAACACTG[C/T]AGAGATGGGAAAAAT	84182
rs370845897	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30803915	TAGGGAAAAGATGGG[A/C]GTCCTTGTTCCTACC	84182
rs370883411	snp	A/C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30792004	AGCTTGCTTTAGCAG[A/C/T]TGGTCCCAAAACATA	84182
rs370927475	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30890037	AAAAGGATTGATTGC[C/G]AAAAGGCCATACAAC	84182
rs370929595	snp	C/T	1.65652e-05	0.0028779	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791304	GCAACAGCTCCCCCT[C/T]CAGGACCTCCCTGGG	84182
rs370966251	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828938	TCCTGGGGACATCCT[A/T]GTAAGAAGACCAGTC	84182
rs370968768	in-del	-/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30825151	GTCCCTTGATTTATC[-/T]TTTTGTCATTGTTGT	84182
rs370975673	snp	C/T	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30860216	TGTGGTGCCCAGGGG[C/T]GGGAGGTCACAGCAG	84182
rs370992066	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30817494	TTCAGTCATTCATGA[A/G]AGCTGTTGAAGTGAT	84182
rs371001924	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30834705	TTGTTTCCCTTATAA[A/C]ACTGGATGCCTTTAA	84182
rs371003653	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30805149	AAAGGTGACTGGCAG[C/T]AGGGCCCCTGCCGGG	84182
rs371013872	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30856119	CTCTGCCTCCCATTG[A/G]AGTTCCTTGGTAGAC	84182
rs371058985	snp	C/T	6.628e-05	0.00575635	utr-variant-3-prime, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30892055	TCATCACCTCATCAC[C/T]GAGGATGACAGCTGA	84182
rs371071909	in-del	-/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852009	CATTTCTTTTTTTTT[-/T]CTTTTAAATCCTGCT	84182
rs371077263	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30799404	ATTTAGGACACAGCA[A/G]CCTGGAATCACTCCC	84182
rs371135723	snp	G/T	0.000103894	0.00720669	splice-donor-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850557	GCCGTTGTTGCACTG[G/T]AAGTGGTTCCGAGGT	84182
rs371147869	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30888177	TGATGCCTCTGGGGG[A/G]ACAGGGCCTTATTTT	84182
rs371170994	snp	C/G	0.198853	0.244712	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771567	GAAAGGTAACGGCTC[C/G]CCCCCTCCAAAGCCC	84182
rs371182857	in-del	-/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30824975	TAATCCAGCTCATGC[-/C]TCTCTCTGGGGGGCA	84182
rs371189586	in-del	-/A			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30866446	AGTGTCACCTGGGGT[-/A]GGTGTGGGTAGGCTC	84182
rs371211577	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872219	AGGCAGAGCTGTGCT[A/G]ACAATGCTTCTTGTG	84182
rs371221478	snp	A/G	0.000163987	0.00905353	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875495	TTCTCTCATCTGCAG[A/G]AACTTGTCAATCTGC	84182
rs371301071	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30775730	TCATCACATTAGCAT[A/G]CAGAAGACATTCTTA	84182
rs371313572	snp	C/G	3.31647e-05	0.00407201	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882929	TTCCCAGACACCACC[C/G]AAACCATCTCTGAGG	84182
rs371326643	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30878779	AGCTCCATCCTCCTC[C/T]CATCCTCCCCAGCTC	84182
rs371346062	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30790778	ATGACAGGTAGTGGA[C/T]TGTGGACTGGTTATA	84182
rs371386019	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30789869	ACTCATCTTTGACGG[C/T]AAGGGAGGATATTTG	84182
rs371436420	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30881973	TGGCAGAGGCCCTGC[A/G]AGCAGCAGCAGGTGG	84182
rs371454713	in-del	-/TTATTTATTTA/TTTATTTATTTATTTA			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30822627	GACGTGCCTGTCTAT[-/TTATTTATTTA/TTTATTTATTTATTTA]TTTATTTATTTATTT	84182
rs371476799	in-del	-/TGCTG			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30862989	GGAGGGAGAGGCCCC[-/TGCTG]CCCCCCTCCCCAGCC	84182
rs371478168	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30816779	TTGTTAAGGCAGATT[C/G]TTTTCACAGGATTCC	84182
rs371514310	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30802706	TTAGTTTGCCTGTTG[C/G]CATTCATTAATTTAC	84182
rs371516368	snp	A/T	3.31378e-05	0.00407036	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836727	CAGTGCTCAAGTTGC[A/T]GACAGCATCAAAACC	84182
rs371525007	snp	C/G/T	0.00263624	0.0362109	synonymous-codon, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771529	GGAGGTGGCCGCCTC[C/G/T]TTGGTCAGGGAGTTC	84182
rs371530664	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30823894	TGTAGGAATGCTCTG[A/C]CAGATAATTTTACAT	84182
rs371619128	snp	A/G	3.31549e-05	0.0040714	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852169	CCGGCTGGAGGGCAC[A/G]CCTTCTCTCCACTCA	84182
rs371640198	snp	A/G	0.000198725	0.00996609	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828697	AAATCAGTTGCTGCC[A/G]TCTGACAAGGTGGAT	84182
rs371642429	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30862170	ATGCTTCCCCCGAGG[G/T]CCTGCAGGAGATGTG	84182
rs371656300	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30801095	AGTGAAAGCCACGGG[C/T]GCACAGATGCCTCTC	84182
rs371686030	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30860712	TGGGCGCCTTGTTAC[A/G]TGCATGCTCCTGCAT	84182
rs371723845	snp	A/G	5.78542e-05	0.00537808	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782215	CAAGCAAAGCCAGGT[A/G]TCTTTTCCCATTATT	84182
rs371734027	snp	A/G	0.000875616	0.0209055	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859383	GTCTTGTTCACTGCT[A/G]CCTCGCTAGAGCCCA	84182
rs371783786	snp	A/C/T	0.000478751	0.0154645	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872316	ACACAGGTCAGGGGG[A/C/T]GCTGTGGGGCCCAGG	84182
rs371837722	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30819598	TTTCTATTATGCTCA[C/T]GGATTGAAGAGTTTC	84182
rs371877710	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30784163	AGGGGCTATGAAGAA[C/G]CTCTTCCTCCGAGGC	84182
rs371919562	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30864137	TCAGCTGCCCAAAGG[C/T]AGTCTTGAAAGTCCG	84182
rs371926512	snp	A/G	1.65811e-05	0.00287929	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791231	ACCCAACCCCAAGAA[A/G]AGAGCCGGAAGGTCC	84182
rs371931347	snp	A/G	0.0103295	0.0711199	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30891165	TTTCCTAGTTCATAT[A/G]TAGTCTTAGGATATC	84182
rs371974120	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30869775	TGAATTTTAAGGGGA[C/T]GCAGTTCATGCCATT	84182
rs371985778	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30887090	TAATTCCAGCTGGGT[A/C]TGATGCCTTCGAGGG	84182
rs372001411	snp	A/G	1.65927e-05	0.00288029	splice-donor-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785993	GCCAGCTCCCCACAG[A/G]TGGGGCTGTTGCTCT	84182
rs372006243	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30813856	AGAAAACAGTCATTT[A/C]TCTGTGCTTTGGGTG	84182
rs372008579	snp	A/G	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30851867	CCATCAGTGAAAACA[A/G]AGGGCAAGTCAGCAT	84182
rs372033107	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30857583	GTTCACGCCATTCTC[C/T]TGCCTCAGCCTCCCG	84182
rs372045019	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30827980	CATTCTGTTTAGAAA[C/T]GATTTTACTTTAGTT	84182
rs372073787	snp	C/T	0.136506	0.222754	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30822624	GGTTGACGTGCCTGT[C/T]TATTTTATTTATTTA	84182
rs372110789	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30877859	TTTTTTTTTTTTTTT[A/T]AGTAGAGATGGGGTT	84182
rs372147358	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30880932	CCTTCAGAGCACAGC[C/G]CCTCTGTCAGAGACA	84182
rs372174751	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30835430	CATGGGAATTATGGG[A/G]GTTACAAAATGAAAT	84182
rs372183801	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30793044	TTTCTAATTCCCATC[A/G]TGGTTTCTTTTTTTT	84182
rs372186543	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30865841	CTCTCAATCGAAGAC[C/G]CTGTGCCTGCATCGT	84182
rs372188146	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30809071	TAAGAAAAAAAAACA[A/G]TGTACCCTATTCCTT	84182
rs372194663	snp	C/G			missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882952	CTCTGAGGACACAGA[C/G]AACGACCTTGTCCCA	84182
rs372221260	snp	C/T	8.32938e-05	0.0064529	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840732	CCAGGCCAGTTCTCA[C/T]TGGCAGCAATGGTCT	84182
rs372263978	in-del	-/C/TTTC			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30877697	CTTTTTTTTTTTTTT[-/C/TTTC]TTGAGACAAGGTCTC	84182
rs372322271	snp	G/T	5.25592e-05	0.00512609	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875674	ACCCAGATGCTCACG[G/T]TCACCACAAGTAGGG	84182
rs372333355	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778199	AGGACTCCTGTGCGC[A/G]AGTCCTGAACTCACT	84182
rs372341051	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853656	ATCTGGCTCCTGCCA[C/T]TGCATCCTCAAGAGC	84182
rs372367374	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30864912	CACCCCGTCAGAGAC[C/G]CTCTGGGGGGAATCA	84182
rs372370693	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30838883	TGGAAGATCAGAGGA[A/C]CTCCAAGATCCCTTG	84182
rs372409211	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30829298	ACTTTTTTTCTCTCT[C/T]TTTCTGTAATTCCCT	84182
rs372437910	snp	C/G/T	0.000231905	0.0107658	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852202	GGACTCATGCACCTT[C/G/T]CTTTCCTTTTTAGGG	84182
rs372469387	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30865646	TTAGCCTCAGCGGGA[A/G]CTGGAGGTGGAGGAG	84182
rs372476549	snp	A/G/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785545	GTTTGCTTGTTTACT[A/G/T]GTCTTATTTTATAGG	84182
rs372484997	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30809308	TAGCTAACAGAAAAA[A/C]TTTAAAAAATAACTG	84182
rs372589175	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30842111	CTTGGCATCTTAAAA[C/T]TTTTTCCAATGGTTT	84182
rs372590460	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30841598	CTTGTACCGAGTCAC[C/T]CTCAGAGCTACAGAA	84182
rs372599401	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30888825	GAGCGGGTTGGTTAT[A/G]TCTGTAGAAAGCCTC	84182
rs372605473	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853947	AGTATCCCTGGGGTG[A/G]CAGGGCTGCTCTGGG	84182
rs372633996	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30821299	GTTCATTCAGTGAAG[C/G]TCTGTGATACTAAAC	84182
rs372698074	snp	A/C/G	0.00522189	0.0508324	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778567	GTATGTGCTTTCTAA[A/C/G]GTGTGGTGTGGAGTC	84182
rs372724224	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30888588	TTGTTGGTTGCATAT[G/T]CAGAGCCCTTCTTAC	84182
rs372744753	in-del	A/TTT			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30796122	GTTGGAGCACTGTAC[A/TTT]TTTTTTTTTTGTCTC	84182
rs372755867	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30832736	GCTGCTCTTAAACTC[A/G]ACCTCAGGTGATCCA	84182
rs372816083	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30806356	ACTTTTTAGCCTCTT[C/T]TAACTTTTTTAGGAT	84182
rs372823460	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30774477	GCAGAATCCCATCTT[C/G]ACCCCCAAACCCTAG	84182
rs372832993	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30884513	TCTGTACAGGACAGC[A/G]TGGGAGGCCACAGGG	84182
rs372834606	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30877948	GCCTTACAAAGTGCT[A/T]GGGTTACAGGTGTGA	84182
rs372857757	snp	C/G	3.53363e-05	0.0042032	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791572	CCAGCCCGCACCTGT[C/G]AGGTGAGTGTGCTAT	84182
rs372872990	snp	A/G	1.76092e-05	0.0029672	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872351	CCTTCCCCCTCCTCT[A/G]TCCCTCAGAGAGGGA	84182
rs372884744	in-del	-/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30855129	GCCTGGAGCAGGGGC[-/C]TGGGGGCCCCCTTTG	84182
rs372922374	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30885426	CTGAGGCAGGAGAAT[C/T]GCTTGAACCTGGGAG	84182
rs372934472	snp	A/T	0.0111196	0.0737302	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30861394	TTAGGTGGGTGCTGC[A/T]GTGAGTGCTGTCACC	84182
rs372935482	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30851065	GTTATCCTGACCCGC[A/G]TCGTCTCTTCACCGC	84182
rs372961611	snp	A/G/T	1.65605e-05	0.0028775	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875509	GGAACTTGTCAATCT[A/G/T]CTCCTGACTGGGAAA	84182
rs372981130	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30788235	TTTTCAGAAAACTGA[G/T]ATATTTTTCTTTGAT	84182
rs372984502	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30820579	ATATTTCACATAAGC[A/G]GAATCATATAATATA	84182
rs373096212	snp	C/T	0.00517822	0.0506191	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30814452	TTTTTATTTTTATCA[C/T]GTCACCATGGACCTG	84182
rs373105216	snp	C/T	0.000173623	0.00931566	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882171	CACATCAGGCCTCTC[C/T]CTCATCCAGGTTGGC	84182
rs373120157	snp	A/C/T	1.68969e-05	0.00290657	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836813	CTTGATTTGAATGGA[A/C/T]ATAGATGGCGTGATT	84182
rs373140004	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850670	CCACCCTGTGCCACA[C/T]GCTGGGATGAGCCCT	84182
rs373153269	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30884483	TGGGGACAGGAGGTG[A/G]CACTAGCCTTGGCAT	84182
rs373160027	snp	A/G	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30835947	AAAACAATATCTGGA[A/G]TATGGCTTACGGTCC	84182
rs373185184	snp	C/T	4.99863e-05	0.00499906	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30883025	TCTGGCTTTGAGCCT[C/T]ACCCTGAATAGCTTT	84182
rs373198093	snp	C/T	0.000195094	0.00987467	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850493	CCGGACCCGCTGCCT[C/T]GTCCTGGCCCTCGCA	84182
rs373214422	snp	C/G/T	0.000496701	0.0157515	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875455	TCTTTCAGTAACTGA[C/G/T]TCAGACTTGATGAGT	84182
rs373216241	snp	A/C/T	4.96808e-05	0.00498377	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785875	TGCATGGGAGAAGAT[A/C/T]GACAAGCTTCACTCG	84182
rs373222739	snp	C/T	0.000215341	0.0103742	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828647	TTTCTCTGTCAGTCT[C/T]CTCTGGTACATTGAT	84182
rs373244068	snp	G/T	2.81845e-05	0.00375386	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850436	TGGGCATAAATGCCT[G/T]CCTTTTCTTGTCCGC	84182
rs373260277	snp	A/C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30879779	CAGGGTATCTTAATT[A/C/T]TTTCCTTCATAGGGC	84182
rs373282711	in-del	-/A			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791904	AAAATTGCAAAAAAA[-/A]CTCAATGTTTTAAGA	84182
rs373291926	snp	A/C	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30813851	TGCCCAGAAAACAGT[A/C]ATTTCTCTGTGCTTT	84182
rs373295305	snp	A/G			synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791419	GGACAGGGCCAGGCC[A/G]AGGGATCCCTCCGAG	84182
rs373341052	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30866228	GCATCTCCTGCCCCT[A/T]TCCACTCACCCAGGG	84182
rs373371532	snp	A/T	0.00318978	0.0398085	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30835729	TAGGGAGCTGGATTC[A/T]CAGAGCCAAGCCCTC	84182
rs373380925	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30787493	AAACTCTATTTGCAA[C/T]CTTGAGCTTAGTCTG	84182
rs373398914	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30862604	CCTCCGGGGCTAGCC[A/G]CTGGCAAAGGCCTTT	84182
rs373418944	snp	A/T	7.9209e-05	0.00629271	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850526	CATTGTGTGGCGGGC[A/T]GGGGGCCGAGAGAGA	84182
rs373430307	snp	A/G	1.65737e-05	0.00287864	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778409	TTAAGATGGTAAACA[A/G]CGATTCAGCTTTCTT	84182
rs373437905	snp	A/C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30870214	GCAGGCTCTCGAGCC[A/C/T]GCTGGGTGAACACGA	84182
rs373458904	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30866797	GTGGGTGGGAAGAGG[C/T]GGGTGGCAGAAGGCA	84182
rs373474586	snp	C/T	0.00438332	0.0466095	upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30770151	GGGCACGGTGGTGGG[C/T]GCCTGAAATCCCAGC	84182
rs373487130	in-del	-/AG			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30884861	TCCATGCAGAGTGAG[-/AG]TCTTAGTGTGTGGAC	84182
rs373491366	snp	A/G	1.66054e-05	0.00288139	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882256	TTCAGCATCCTCTTT[A/G]GCCTGCAGCCGGGGC	84182
rs373491679	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30817097	AGGGAGGTAGAGGAA[G/T]CCCCTCCGGAGGCTC	84182
rs373526363	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30879552	TCTCCCACCTCAGCC[C/T]GCACCACTCTCTCCC	84182
rs373582763	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30805846	TTAAGGAATAGGGCC[A/G]TTTATTCAGGACAAG	84182
rs373611161	snp	A/G	7.99904e-05	0.00632367	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850568	ACTGTAAGTGGTTCC[A/G]AGGTCTGTGTTGCCG	84182
rs373623044	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853571	TCCCACCCTGGGATG[A/G]CGAGGAAGCTGGGAA	84182
rs373631842	snp	C/G	0.000390092	0.0139604	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771602	AGTGGCTCTAATTTG[C/G]GGGGATCATCGGGGT	84182
rs373632877	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875986	ACAGGAACTTGAGGT[C/T]TTAGGCCTCGTGTTA	84182
rs373666086	snp	A/G	1.65622e-05	0.00287764	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828706	GCTGCCGTCTGACAA[A/G]GTGGATGGTGAGCTG	84182
rs373699662	snp	G/T	0.0023933	0.0345097	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30832961	TATATCTTTTTCTTG[G/T]GTATGTTCTTGCAAA	84182
rs373700442	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30880798	GTGAGGCTTCGGTGT[C/G]GGGGGAGGGGACACT	84182
rs373722662	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30841850	GATTTTAAAACCATA[A/G]CTTAATCTTGCCAGT	84182
rs373726073	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30808801	GTTACAGCTGGTTTT[A/G]GAGCCCCGTCGTCGG	84182
rs373727677	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30864503	TGGGAATTGGTGTCT[A/G]TTCTTTTGTCTCTTC	84182
rs373735086	snp	C/T	1.66153e-05	0.00288225	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30883004	ACCAAGTGAGTCAAG[C/T]CCCTCTCTGGCTTTG	84182
rs373738881	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30792484	GGGAGAATTTACTGG[A/T]GAAATTTTCTGTGCA	84182
rs373764264	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828089	AGGTGGACCCTTTTA[A/G]GAAAGCTCTGTGTGC	84182
rs373822614	snp	C/T	1.65663e-05	0.002878	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859291	GCTGCATCCTGCTCA[C/T]CCTTTCTGCCATCCT	84182
rs373827296	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30802045	TGGAAGGAAGTTGTT[A/G]GGCTCTGAGATAATA	84182
rs373828633	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850336	AGGTGGCCCCTCTGC[A/T]GGCCAGAGAAAGAAC	84182
rs373832336	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30780297	ATTTTGCGCAGAGAG[C/T]GAGACAACTACCCAG	84182
rs373841379	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30819963	CTGGAGTGCAGTGGC[A/G]GGATCTCGGCTCACT	84182
rs373860037	in-del	-/TTGT			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30862866	TTTTTTAAACTATGT[-/TTGT]AATGAAAACAAAATC	84182
rs373863167	snp	C/T	8.28054e-05	0.00643396	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30891950	TCTCTCCTCACTCTA[C/T]GCTTAGGTGGAAGGG	84182
rs373908456	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30889045	AAAGATAGAGAGGGG[C/T]GGGGTGAAGGGGCCT	84182
rs373917565	in-del	-/GGTGAAGGATAGGAG	0.0126979	0.078662	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30829997	AGGAAAGGAGAAGAA[-/GGTGAAGGATAGGAG]GCCATGGAACCCAGT	84182
rs373920173	snp	G/T	0.000169986	0.00921759	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839222	AGACCCTTCTGTTTG[G/T]TTCCAGCTTTTGCTG	84182
rs373937023	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828412	GCTTGGCAAACGCCA[A/G]CCTACAGAGCTGACC	84182
rs373958195	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30860633	CCATCCATGCGGGGG[C/T]CCTCTGGCTCTGGGA	84182
rs374016835	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30863346	GTGTATGTGTACATT[C/T]GTGGTGGTGTGATAG	84182
rs374026488	snp	A/C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30877078	GTCCCAAAGACTTGC[A/C/G]GGAAAAAAGAATGAG	84182
rs374069900	snp	A/G	0.00478085	0.0486577	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30832621	TTCAAGTGATTCTCA[A/G]GCCTCAGCCTCCTGA	84182
rs374200604	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30876814	AGGCCTCATTCACCA[C/T]CTATCCTCAGAACCA	84182
rs374211744	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30834307	GTGCACCTGCAGGCT[A/C]AACACCACATGGTAG	84182
rs374273914	in-del	CGGT/GG			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30812280	GTGTTGAGGGGGGGG[CGGT/GG]GTATGTATGTATGCA	84182
rs374288634	snp	C/G			upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771223	GACCAGGGCCAGGGT[C/G]AGAGTGAGGCCCCGA	84182
rs374313415	snp	A/G	0.0119091	0.0762411	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30873103	GCTCTGGAAACCTAC[A/G]TGGGCACCATACAAG	84182
rs374331777	snp	A/G	0.00318978	0.0398085	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875710	TGACTCTCTGGAGCA[A/G]TGAGGAGGGAAGTGG	84182
rs374350045	snp	C/T	6.28239e-05	0.00560429	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850546	GCCGAGAGAGAGCCG[C/T]TGTTGCACTGTAAGT	84182
rs374354751	in-del	-/AACA			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30809070	TAAGAAAAAAAAACA[-/AACA]GTGTACCCTATTCCT	84182
rs374370162	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30823785	CTCATGTGTTTAAGA[G/T]TTTTTTGTTTTGAGC	84182
rs374410519	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30829300	TTTTTTTCTCTCTCT[C/T]TCTGTAATTCCCTAC	84182
rs374435049	snp	A/C/G	1.65858e-05	0.00287969	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791432	CCGAGGGATCCCTCC[A/C/G]AGGACACCCCAGCAG	84182
rs374457376	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30861361	GCACATGAACGCATC[A/G]AGTCCACAGCAGCCC	84182
rs374457719	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30837297	TTGCTCACCATGCTC[A/G]GCTACCAGGGTGGCC	84182
rs374472979	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30816298	TTCTGAGTCTGAGAC[A/T]GTGGTAAATTTGTTC	84182
rs374476505	snp	C/T	0.152724	0.230298	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771573	TAACGGCTCGCCCCC[C/T]CCAAAGCCCAGGAAG	84182
rs374490373	snp	A/C/T	0.000149073	0.00863226	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852278	ATGGAGTCTTAGAAA[A/C/T]AGTACGACTTTCTGG	84182
rs374557734	in-del	-/A			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30825568	GGAAGGATGTGGAAA[-/A]TAGAGGCAAGACCAA	84182
rs374569686	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30772835	TTTTAAGTCTGGGTC[A/G]CTGAAAAAAACTCTT	84182
rs374575606	snp	C/G	0.000163987	0.00905353	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791382	GCCCTCCCCATCTGC[C/G]CAGCAAACGGCTGCC	84182
rs374659097	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30889605	GCTCTGATATGGATA[A/C]ATTCCATCAAAGTGG	84182
rs374667741	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30860992	AGATGCACATACGTG[A/G]CCACACACAGAGACA	84182
rs374690367	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782688	AGCTTGGGAGATGGA[A/G]TGAGACCCTGTCTCT	84182
rs374694940	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30874168	CTTGTGTCACAGGCA[A/G]CGCCAGCTGTGGCAG	84182
rs374713305	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30817022	ATAACCCAACCCTTC[A/G]TGAGACCTCATGTTC	84182
rs374724043	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791839	CATTGGAAGAACAAT[C/T]GTCTTGTGCCACGCA	84182
rs374782356	snp	A/C	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30886597	CAAGGACTGTGGCTT[A/C]CGCTTTTGCTGTCCC	84182
rs374795355	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30854717	GTCAGACTGCCTTCC[A/G]CAGAACTTTCCCAAA	84182
rs374824384	snp	C/T	1.65751e-05	0.00287876	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882948	CCATCTCTGAGGACA[C/T]AGACAACGACCTTGT	84182
rs374883588	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30838424	AGGAGGTTCTTACGC[A/G]TGGTAGAGAGTTGTA	84182
rs374910173	snp	A/G	0.000116039	0.00761617	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836744	ACAGCATCAAAACCA[A/G]TTGACCTCTCAGTAG	84182
rs374913777	snp	A/C	1.75665e-05	0.0029636	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882161	GACGGCATTTCACAT[A/C]AGGCCTCTCCCTCAT	84182
rs374925838	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30858670	ATATATATATATATA[A/T]AAATTTAAGACATGC	84182
rs374963616	snp	C/T	0.00027115	0.0116405	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882349	CAGCAGGAGCAGATC[C/T]GGCTGACCATTGGTG	84182
rs374971444	snp	C/T	0.0170251	0.090679	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30819985	CGGCTCACTGCAAGC[C/T]CCGCCTCCTGGGTTC	84182
rs374974001	snp	A/G	1.65633e-05	0.00287774	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778456	AAGACATGTGTGACC[A/G]TGGACCAGGAACGCC	84182
rs375113395	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30842620	TCATGGCACCTATGA[C/T]TGAACAGGAGAGCCA	84182
rs375131713	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30809443	CTTAACCCAGCAGGT[G/T]TCCTAACAGGGGATC	84182
rs375225177	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30813221	CTCTGTAGAAGATTC[A/G]TCGTCAGGAGAAAAG	84182
rs375227763	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30781639	AAATGAAGGGATATA[C/T]ATTTTATAAAGTTAT	84182
rs375287585	snp	C/T	4.96816e-05	0.00498381	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30891984	ATCAGTGAACTGGAA[C/T]GGCTCAGACCCCATC	84182
rs375306878	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30823233	TTCCCTTTTGCAATT[A/G]ATAAGTAATCTGAAA	84182
rs375313491	snp	C/G/T	4.96827e-05	0.0049839	missense, stop-gained, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785954	TCTGGTCTGATTGTG[C/G/T]GAGGCATGATGTCTG	84182
rs375315394	snp	G/T	0.000437904	0.0147905	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828795	AAGGGGTCCTCGTTG[G/T]CTCTGTCTGGGAGAT	84182
rs375320849	snp	A/G	0.000215262	0.0103723	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875546	TCCAACGTTTTCAAC[A/G]ATGTGGTTGAGCTGG	84182
rs375329768	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30887153	CCCCACTCCCTGCGG[A/G]ACCTCCCGTTCAGCT	84182
rs375338983	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30822105	TGTAAATATTTCAGC[A/G]TGCGTCTCCTAAGGG	84182
rs375362458	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30809807	AAGGGGGAAAAAAAA[A/G]GGGGGCAGAATTTAT	84182
rs375387727	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30878777	AAAGCTCCATCCTCC[C/T]CCCATCCTCCCCAGC	84182
rs375402826	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852001	CTTTTTTCCATTTCT[C/T]TTTTTTTTCTTTTAA	84182
rs375404724	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30886315	AAGACTTGGCTCCTG[C/T]TCTCAGAGAGTTTGC	84182
rs375415605	in-del	-/CTC			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30866956	CATCCTAGCCCTCTC[-/CTC]TTACTGCTTTGAGAA	84182
rs375416712	snp	A/G	0.000437904	0.0147905	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840903	AGTCTTCCCCAGAGT[A/G]TCCAGAAAAAACAAG	84182
rs375428635	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30796247	TCACTGTCACATCTG[C/T]CTCTTTTTTATCTGG	84182
rs375432478	snp	G/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30851564	TGTTTTTGTTATTAT[G/T]ACTGTCACTTGTCTT	84182
rs375458993	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30890866	TCTGTTGGAAAATGC[A/C]ACTGTGTTACTTTGG	84182
rs375478983	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30819984	TCGGCTCACTGCAAG[C/T]TCCGCCTCCTGGGTT	84182
rs375487976	snp	A/C	0.000732677	0.0191259	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882371	CCATTGGTGCGGGCC[A/C]TCACCCCCCCACCCA	84182
rs375500119	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30787632	CAGCACAGCTGGCAC[C/T]AGTGGATGGAGGTTG	84182
rs375510284	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30827265	TTTTCAGAAAGGGAC[A/G]CTGAGGCACAGCAAG	84182
rs375544404	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30796831	GATGTCTTGCTCTTC[A/G]TGTTACAGATCCTTT	84182
rs375567092	snp	C/T	1.66142e-05	0.00288216	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840748	TGGCAGCAATGGTCT[C/T]ATTCTTTGCAGGGTG	84182
rs375606000	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30833297	GGGAAGCCTCACAAT[C/T]ATGGTGGAAGGCAAG	84182
rs375619928	snp	G/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30869662	GTCAGATTGCATTAG[G/T]GCCTACCCTAATGGC	84182
rs375628242	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30887013	GAAAGAACTCATAAC[C/T]GGAGCCTGGGGCTGG	84182
rs375637605	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30838276	AGTGAACTCATTATC[A/C]GCCAGAAGTCTGGAG	84182
rs375668037	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30803916	AGGGAAAAGATGGGC[A/G]TCCTTGTTCCTACCC	84182
rs375718826	snp	C/T	0.000500391	0.0158097	utr-variant-5-prime, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771481	CCTCGTGGGCAGAGC[C/T]AGAGCCAGAGCCATG	84182
rs375724016	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30870598	CCGTGTTTGGCCATG[A/G]TTATTAAAAACCACA	84182
rs375802699	snp	G/T	3.32812e-05	0.00407915	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30883017	AGCCCCTCTCTGGCT[G/T]TGAGCCTCACCCTGA	84182
rs375867200	snp	A/G	0.000100578	0.00709077	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836626	TCCGTGAGTCATAAC[A/G]AAGGGCTCACATGGC	84182
rs375904362	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30883922	CCCACTTTGTCATCT[G/T]TAAAATGGGGGTGAT	84182
rs375932278	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30890164	GTAACATTCCTGGCT[C/G]AGCGTGTTTTCCAGC	84182
rs375998529	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30864201	TTTTAGAACAGCACA[A/G]GCTAGGTGCTGAGGG	84182
rs376014276	snp	A/G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30798659	CCGCCACCACGCCTG[A/G/T]CTAATTTTTTTTGCA	84182
rs376014500	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30832748	CTCGACCTCAGGTGA[C/T]CCACCCACCTTGGCC	84182
rs376021005	snp	A/G	0.00597247	0.0543191	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30815871	GTGTGTCTCCCCAAG[A/G]GAAGAGCAATCAGTC	84182
rs376063962	snp	C/T	9.9807e-05	0.00706354	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839280	TTTTTCCTTTAGTAA[C/T]ACAGCCTCATTAAAA	84182
rs376096463	snp	A/G	0.00557542	0.0525036	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836974	TTCCCTCTCCAAGAC[A/G]AAAGGTGAGGGAGGA	84182
rs376110782	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853009	CAGCCTGTTGGCTTC[C/T]ACCTGGCCTGGCTAT	84182
rs376189427	snp	A/C/G	0.00072845	0.019073	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875535	GGAAAGCTGTGTCCA[A/C/G]CGTTTTCAACGATGT	84182
rs376233756	snp	A/G	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872365	TGTCCCTCAGAGAGG[A/G]AGAGGTCCTCCTCCC	84182
rs376238682	snp	A/T	0.000159987	0.00894248	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853455	TTCAACAAAGCATTC[A/T]TCAGGTATGAAGCAT	84182
rs376244311	snp	C/G	0.000118756	0.00770479	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882193	CAGGTTGGCTGCTTC[C/G]TGAAGACCCCGAGGT	84182
rs376245817	snp	A/G	1.65704e-05	0.00287836	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791341	TAGTGAACTGACCGT[A/G]GAAAGGCAGAAAACC	84182
rs376252027	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30889393	CCAGAACCTGCTCAG[C/T]TGTATAAGCCAGAGC	84182
rs376254800	snp	A/G	3.28111e-05	0.00405024	missense, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771555	AGTTCCTCAGCAGAA[A/G]GGTAACGGCTCGCCC	84182
rs376291776	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30799719	TTTTAACAAGCTTTT[C/T]AGGTGATGTCATGCG	84182
rs376307796	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30871993	GTAGGCAGAGCCCTG[C/G]TGCGGCTGGAGTGGA	84182
rs376370591	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30787653	ATGGAGGTTGGTATG[A/G]GAGCCTTCCATTAGT	84182
rs376378790	snp	C/G	3.31549e-05	0.0040714	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882965	GACAACGACCTTGTC[C/G]CACCCCTCGAGCTCT	84182
rs376403376	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30811378	AATGATAAAAAGCTT[C/T]ATCGCTACCTTCATT	84182
rs376411918	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30779661	CCTTCTCTCAGGAGG[G/T]GGAGCTGTGAGCCAG	84182
rs376413412	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30878692	TTCTTTCATGACCTG[C/T]GAGGCATGTTCATTG	84182
rs376429103	in-del	-/A			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30793158	ATATATTGTTTATTT[-/A]ATTGTTTATATATGT	84182
rs376430692	snp	C/T	4.968e-05	0.00498373	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875482	GAGTCTTTCCCCTTT[C/T]TCTCATCTGCAGGAA	84182
rs376449663	snp	A/C/G	1.65674e-05	0.00287809	synonymous-codon, missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791251	CCGGAAGGTCCCTGA[A/C/G]CTCTTTGTCTGCACC	84182
rs376470548	snp	C/T	0.000480319	0.0154896	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852283	GTCTTAGAAACAGTA[C/T]GACTTTCTGGAAAAT	84182
rs376500004	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30866198	TGGGAGGTCTCAAGA[A/C]CCTCGGTCCTGTGTG	84182
rs376520188	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30883098	ATAGGTTCCTGGACC[A/G]CCCTGATTCAAAGAG	84182
rs376530943	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30823647	TTCCATTCCTGTTTT[C/T]AAAAAGTTTCTCTAA	84182
rs376532592	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30870302	GTGATGCTTATCGGC[C/G]CCCCCTCAGGACCCT	84182
rs376602775	snp	C/G/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30891324	TCTCACCTACAGTAA[C/G/T]TTTTCGTTTTGCAAC	84182
rs376617307	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852998	AACTCAGGACACAGC[C/T]TGTTGGCTTCCACCT	84182
rs376622478	snp	G/T	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30887418	CCTCTCCTGAGCTGC[G/T]GTGAGGTTGAGAGAA	84182
rs376629083	in-del	-/A			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30810344	AATGTAAAACTATTG[-/A]AAAAAAAAAAAAAGT	84182
rs376669815	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30804405	AATCTAAATACATGG[C/T]ATTTAATTTTATTCA	84182
rs376690971	snp	C/T	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30863843	ATCTCGAATTGCTTC[C/T]GGTAAATCTCATGCA	84182
rs376702905	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30863120	GACCAGATGATCGCC[A/G]AGGGCCTTCCTGTTC	84182
rs376704141	snp	G/T			upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771314	TCCGAGACGCGAGTT[G/T]GCGGGACGCTCCACC	84182
rs376714501	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30865652	TCAGCGGGAGCTGGA[A/G]GTGGAGGAGAGAGGG	84182
rs376741776	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30806815	TTCCTACCCTCTTCT[C/T]TTCTAGAAGGTTTTC	84182
rs376757314	snp	A/G			synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850499	CCGCTGCCTCGTCCT[A/G]GCCCTCGCAGACATT	84182
rs376777421	in-del	-/TGTTTT			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30847751	TTTTGTTTTTGTTTT[-/TGTTTT]AGAGACAGGGTATCA	84182
rs376786587	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30835792	TGCCGGCACCATTGC[C/T]TTGGCATTGTTTCTC	84182
rs376805409	in-del	-/AA			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30786631	CCCTGTCTCAAAAAG[-/AA]AAAAAAAAAAAAAAA	84182
rs376810984	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30777471	ATTTCTTTCCATTTC[C/T]CTTCCCTACGGCCTC	84182
rs376845477	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30844581	GAGGGCCTGCTGTCG[A/G]GGGCCTGGAGAAGAG	84182
rs376874046	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30783487	CATTATTGGAACACT[A/G]AGCATGAGGGAGTTA	84182
rs376902616	snp	A/G	3.32386e-05	0.00407654	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882267	CTTTAGCCTGCAGCC[A/G]GGGCTCCTGCGTGAC	84182
rs376904893	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30797502	CTGGACGCAAATGCC[A/G]ACAGCAGTTGTGCAC	84182
rs376907623	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30819994	GCAAGCTCCGCCTCC[C/T]GGGTTCACGCCATTC	84182
rs376945313	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30788341	ATCAGTTTCGCTTGA[A/T]ATGTCTTGCACTTTG	84182
rs377007335	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30795072	GTGGGTTCTTTGGAG[A/G]CACCTCACTTGTGTT	84182
rs377107727	snp	G/T			upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30769994	TTTCAAAACTCCTGT[G/T]TTGGGCCGGGTGCGG	84182
rs377125728	snp	G/T	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839123	TCAAGAACAACTTCT[G/T]CAGGAATATGCACAC	84182
rs377203098	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30871398	AGGGAGTTACATTGG[C/G]GTGGCTAAAAGGAAC	84182
rs377214150	snp	A/G/T	6.77603e-05	0.00582033	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791544	TGGAAAGAGCGTTCA[A/G/T]ACGGCAGGGCAGCCA	84182
rs377218227	snp	A/G	3.35531e-05	0.00409578	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872260	TCCGCCAGGACTTTG[A/G]TGTCCCCACCAGCCA	84182
rs377239980	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30841624	CAGAACTTCTGGCAA[C/T]TGGCCTTTTTTAAAA	84182
rs377250481	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30812918	GGTCCAGCTGCTTCC[A/G]ATGGTTTTCCATTTG	84182
rs377280430	snp	A/C/G	8.28046e-05	0.00643399	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30891951	CTCTCCTCACTCTAC[A/C/G]CTTAGGTGGAAGGGG	84182
rs377300898	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30847466	GGCTGGTTCCTGAAA[C/G]CAGGTGCCCACGGCA	84182
rs377308901	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30815629	AGTGGTTACTCAATG[A/T]ATTTGAGTGTGTTCC	84182
rs377310741	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30881181	CAGGGTCAGGAGAGG[C/T]GCTGGCCAAGAAGTG	84182
rs377315870	in-del	-/TT			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30776981	ATTTCTTTTCTTTTC[-/TT]TTTCCTTTTCTTCTT	84182
rs377377055	snp	C/T	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30855466	GATCACCTGGTCACA[C/T]TCCCAGCTGAAGCAG	84182
rs377377562	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30842990	TAATAACTCCACTGC[C/T]AGCTGGTGCTCTTGC	84182
rs377409260	snp	A/T	1.66638e-05	0.00288645	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30883026	CTGGCTTTGAGCCTC[A/T]CCCTGAATAGCTTTG	84182
rs377426480	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30888016	CGTCCCTGGATGCTT[C/T]TCTACCAGTCAGGAG	84182
rs377447844	in-del	-/CTTTCTTAAGC			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30800993	CAGGCCCTACCAGAC[-/CTTTCTTAAGC]AGTCCAGGGGGAGAG	84182
rs377460893	snp	C/T	3.31203e-05	0.00406928	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785878	ATGGGAGAAGATAGA[C/T]AAGCTTCACTCGGAG	84182
rs377497800	in-del	A/TGAATC			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839658	GGCCTTCTTAGGCTG[A/TGAATC]TCATTGAGAGATTCA	84182
rs377520823	snp	A/G/T	4.96844e-05	0.00498399	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778475	ACCAGGAACGCCCAC[A/G/T]CTCTGACCTCAGCAT	84182
rs377528895	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30822507	AATAACATTATCTGA[A/C]ATGTAGCCCATAATC	84182
rs377535550	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30807164	ATTAGAGGCTGTTTG[A/G]CAAGGCTGAGAGCCA	84182
rs377553266	snp	C/T	1.69588e-05	0.00291189	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839327	ACAAGGCAGGTTGCT[C/T]CTAGGTTTCCTTGGG	84182
rs377600596	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859823	GAGAGGTGGCAGGGC[A/G]GCTTGTCCTAATCTC	84182
rs377613037	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30816299	TCTGAGTCTGAGACT[C/G]TGGTAAATTTGTTCT	84182
rs377681057	in-del	-/TG			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778763	CGCCCATTGGCGTGT[-/TG]TGTGTGTGTGGTTGT	84182
rs377690487	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30775194	AGACCCTGCAGGTTA[A/G]GTCACGCTCATGACT	84182
rs377714422	snp	A/G	4.96816e-05	0.00498381	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785822	CACAAAAGTAAGCCC[A/G]TGCAGACGGTCCCGG	84182
rs377733583	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859918	AGCCTGCTCCACAGC[C/T]GGAGTTTCCCCATGA	84182
rs377760897	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30793147	ATATATATTATATAT[A/T]TTGTTTATTTAATTG	84182
rs386409826	in-del	-/AA			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30810175	CAAGACTCTGTTTCA[-/AA]AAAAAAAAAAAAAAA	84182
rs386711768	in-del	AGGCTCT/GGCTCTGAGATAATATTTGG			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30802046	GGAAGGAAGTTGTTG[AGGCTCT/GGCTCTGAGATAATATTTGG]GAGATGAGTGTGAGA	84182
rs386711769	in-del	ACG/CC			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30820602	ATAATATATAAACTT[ACG/CC]GTGTCAGGCTTCTTT	84182
rs386711770	in-del	AGGCA/TTTTAAAAGAG			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30833367	AGAGAGAGCCTGTGT[AGGCA/TTTTAAAAGAG]AGCTTCTGTTTTTAA	84182
rs386711771	multinucleotide-polymorphism	CA/GG			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30841012	AAGGCCTGCGCAGAC[CA/GG]GTGTTAAGGGGACTT	84182
rs386711772	multinucleotide-polymorphism	AT/CA			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30845715	GATGTTGCCCACCAC[AT/CA]CTGGTGGGGAAATGG	84182
rs386711773	multinucleotide-polymorphism	CT/TG			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30848165	ATGGAGTTTTTCCAG[CT/TG]TAGGTGTTCTAGGCA	84182
rs386711774	multinucleotide-polymorphism	CA/TG			missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875647	CTTTGAGCATTACAA[CA/TG]TGTGCCAGGTACCCA	84182
rs386711775	multinucleotide-polymorphism	AC/CT			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30889642	CCCAAAACCCAATAG[AC/CT]TCCTCTGGATCTGCT	84182
rs397705802	in-del	-/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30821771	TATCTCTCTCCTGAT[-/T]GGTGATATTCTGAGT	84182
rs397717211	in-del	-/A			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30796911	CAAAAAAAAAAAAAA[-/A]GACCCTGTCAATTCA	84182
rs397753596	in-del	-/T	0	0	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30793432	TGCTTTTTTTTTTTT[-/T]GGAGACAGGGTCTCA	84182
rs397782700	in-del	-/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30863966	TCCTGGGGTCAGGAC[-/C]AGCTCTGAACCAGAC	84182
rs397938512	in-del	-/A			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30891429	AAACAAAACAAAAAA[-/A]CTGTCGTGTTACTGC	84182
rs397954035	in-del	-/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30877699	TTTTTTTTTTTTTTT[-/T]GAGACAAGGTCTCAC	84182
rs398004239	in-del	-/TTTCTTTTCTTTTCTTT	0	0	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30776984	TCTTTTCTTTTCTTT[-/TTTCTTTTCTTTTCTTT]CCTTTTCTTCTTTCT	84182
rs398004241	in-del	-/T	0	0	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30790476	TTTTTTTGAGATGGT[-/T]GTCTTGCTGGCCCAG	84182
rs398004242	in-del	-/A	0	0	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30806496	CATTTAAAAAAAAAA[-/A]CAGATGGATATATTC	84182
rs398066740	in-del	-/ACTA			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30847545	TTCCAGTTTTTACTA[-/ACTA]TCTGATCTGAGTAAA	84182
rs398085681	in-del	-/A			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30891428	AAAACAAAACAAAAA[-/A]ACTGTCGTGTTACTG	84182
rs527268695	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30854073	AGATCACAGGGCTCC[A/G]GGAAGTCATGGCAGA	84182
rs527277300	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30801544	TTGATCACATTTTAC[C/T]CTATACATGTGCCCC	84182
rs527286585	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30878032	GTCCCCAAGTCCCTC[A/G]GGCCCTACACAGTTA	84182
rs527286753	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30884501	CTAGCCTTGGCATCT[G/T]TACAGGACAGCGTGG	84182
rs527300606	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30884175	AGGGTTGATGCCCAC[C/G]ACAGGAAAGCGAGCC	84182
rs527311513	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30856476	TAGGACTGGGGGCAA[C/T]GCTGGCATAAATGTA	84182
rs527313766	snp	A/G	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30843561	GGAAGAGCCGACTCT[A/G]CTCAGGGCACAAGGC	84182
rs527332153	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30837360	ATGGAATGTCATTCC[C/T]GCTGTCCTCTTCTGG	84182
rs527337462	in-del	-/TA	0.00318978	0.0398085	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30788015	TAATGAAAAAATAAC[-/TA]TATTTTTCAAAACAA	84182
rs527396901	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30814355	AAATTTTACCAGTTG[A/G]GGTAGACATAATCTT	84182
rs527402018	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30848815	GATTTGAAGGATTTC[C/G]AGTGTCAGAGGCTTG	84182
rs527412022	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30884290	CGACATGCTTTGTCC[A/G]TCCGTCCGTCCATCC	84182
rs527436783	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30776330	GCTCAGGGCCTTTGC[A/G]CTTGCTGTTCCTTGC	84182
rs527462038	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30775720	CATCCACTAGTCATC[A/C]CATTAGCATACAGAA	84182
rs527469151	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30812968	TACCTTTGGTCAGCG[C/G]TCTTCCTGGCGTCTG	84182
rs527507907	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30816200	GTCTCATATGCCAAA[G/T]TGGAAGAATAGGGAA	84182
rs527512091	snp	A/G	0.00438332	0.0466095	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30789509	TACTACATCACTTCT[A/G]TATTTAAGAATGACT	84182
rs527550658	snp	G/T	0.000260907	0.0114186	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30781955	TATAAATTAATGATT[G/T]TTTTTTCTCTCCCAA	84182
rs527587129	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30788302	GTGAAATCTTAAACC[A/G]TATCAGTGAACTTTT	84182
rs527596319	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30781130	AGTCTGCAAAATCAC[A/T]GAGTGCCCCATGTCC	84182
rs527603157	snp	A/C	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30832765	CACCCACCTTGGCCT[A/C]CCAAAGTGTTGGGAT	84182
rs527632880	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30865693	TGCTGCCATCTTAGG[C/T]CTTTGTTGTCTTGTG	84182
rs527634638	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30830029	CATGGAACCCAGTCA[C/T]GGAGAGAGTTCATGA	84182
rs527655977	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30855693	CCCAGGGCTTTGATG[A/G]AGCCTAACCAAGACA	84182
rs527664707	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30814949	AGGAAAATACTTCAT[C/T]CTAGAAGTTGTTTTA	84182
rs527668055	snp	G/T	0.00199481	0.0315187	upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771126	GTCCTCCAGAAACAA[G/T]GAGGCAGGTATTCTT	84182
rs527677961	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30891397	GTTATACTCCGTGCT[G/T]CTTCAGGTTAAAAAA	84182
rs527735386	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30881299	ATGCTAGCAACGTGC[C/T]GAGGGCCCTGGTGCT	84182
rs527749297	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30883978	GAAGAGTGTCTGGGA[C/T]GTTACTAAGTGCTCC	84182
rs527750198	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30784126	AGCAATTAGCACAAG[C/G]ATTCAGAGGTGGAGG	84182
rs527752787	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30777170	CTATGGCACCATGCC[C/G]AGGCCCCCGGTGGTT	84182
rs527759994	in-del	-/TGAAA	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30798420	GGGGTTGCCGTTCCC[-/TGAAA]TGAAGACTGTGGGAG	84182
rs527767932	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30861596	AGGCCTGACTCTCTA[C/T]TCCTCTGAATAGAGC	84182
rs527808968	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30860247	GAGACACTTCTTTCC[C/T]GGCCTGGTTGGGTCT	84182
rs527931932	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30843215	TTATCCAAACAGGGA[G/T]GGGAGGCAGAATGGT	84182
rs527934209	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30833653	TTTCAGCATTAACCT[A/C]AAAGTCCACAGTTTA	84182
rs527944436	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30838822	AACTTCGTATCCTAG[A/G]TGGTTCTAATGTGAG	84182
rs527989997	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30890329	TAGACTAGGATGAAC[A/G]TGACATCCTTACATT	84182
rs527993733	in-del	-/T	0.00239712	0.0345371	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30823510	TAGCAGACTCATGAA[-/T]TTTTTTCAATATTTA	84182
rs527995363	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30843951	GGCTGGACCAGAGGA[C/G]GTCTGTGCCATGCAG	84182
rs527996040	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30799800	CGGTACATGTAATTT[A/G]TTGGGGGCATGCTCT	84182
rs528008932	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872647	TCTCAGGCATGGGCC[A/G]GGGGACCCTGGGTCC	84182
rs528011103	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30802124	TCCTGTATTCCTTTT[C/T]TTCTCACTCCAAGAT	84182
rs528064377	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30817654	TGAAAAGCGGAAGCC[C/T]GGGTTCCCGAAGTTT	84182
rs528069208	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30780200	GTCCTGTGGAAAGAC[G/T]GGTGACCCAGGCAGC	84182
rs528141544	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30779682	TGTGAGCCAGAGAGA[A/G]TTGGCTATCCAAGGT	84182
rs528145267	snp	C/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30831393	AGTCATCTCTTACCT[C/G]TGTCCCACATCATCC	84182
rs528155988	snp	C/G	0.00318978	0.0398085	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30786188	GCCTTGAGCAGGCCT[C/G]CTTTCCTGCCCTTAG	84182
rs528178097	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30776311	CACTGGCCTTTTGCA[A/G]CTGGCTCAGGGCCTT	84182
rs528179503	snp	C/T	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30774174	CCATTTCATACCTTC[C/T]CTCTCTTCAAACCCT	84182
rs528193914	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30830697	TGACATGTGGGGATG[A/G]TGGGAACTACCATTC	84182
rs528234011	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30870150	CTAAGGATGCAATTA[C/T]CATTTCCTCCCATTG	84182
rs528236726	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30870637	TTTTCCCCAAGTATT[A/G]TGGAGCTGGAATTGC	84182
rs528263100	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30792044	ACATGGCCAGGCAGA[C/T]GTGGCTAAGAGTTTC	84182
rs528383993	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30835632	AAAGGAGGCTGTAGC[A/G]TAAGATATAAGCTGT	84182
rs528395687	snp	C/T	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30867692	TATCTCTGGAGGTCA[C/T]TGCTGGTGGGTGGGG	84182
rs528403437	snp	A/G	0.000132804	0.00814767	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840838	GGAGATAGCAAAGCC[A/G]ACTGTGCTCAGTAAG	84182
rs528406348	snp	A/C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30881617	AAGGGTATGATCTGT[A/C/T]GAGCATGAGGCAGAG	84182
rs528409223	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30846281	ATGGCTCCATGGGCA[C/T]GTCACAGTGGACAGG	84182
rs528421354	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30874768	GGCTTTCCCTGCCCT[G/T]TTAAAACCCCACCGT	84182
rs528430273	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30865008	TTGGAGGTTTAAGTG[C/T]GCTGTTCTGAACGGG	84182
rs528517164	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30877289	CTCTGGTTTCATTCT[C/T]GGGTCGAGGGCGTTG	84182
rs528558927	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30837099	CCCCATTAGAGCAGC[A/G]CTGCTCCTGTACTGG	84182
rs528570831	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30842178	AAAATGCTAATCAGA[A/G]GCACAGCAATGTAAC	84182
rs528605066	in-del	-/T	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30802119	TCTTTCCTGTATTCC[-/T]TTTTTTTCTCACTCC	84182
rs528630619	snp	A/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30841648	TTTAAAAAAAAAAAA[A/T]TTAGTTAAAATATAA	84182
rs528681122	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30806307	TTGGGTGCAAATCCT[A/C]GCTCTGCCATATACT	84182
rs528693681	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30799396	GTAAATGGATTTAGG[A/G]CACAGCAACCTGGAA	84182
rs528748973	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30888190	GGGACAGGGCCTTAT[C/T]TTCCACCATGAAGTG	84182
rs528761621	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30847301	ACTAACTGGAAGCCA[A/G]TGAAAAGAATGAGGA	84182
rs528762818	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853237	CATACAGGTATGGCC[A/G]TGCCTCTCAGCCCTG	84182
rs528819419	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30867873	TGGTGTTTTCAATAG[A/C]GTCATGGACCAGGCA	84182
rs528849400	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30797358	GGGGAAAAATAAATC[A/G]TGGAAGAGTGACAGG	84182
rs528872952	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30874106	CACTGGTCAAGGGCC[A/G]TTCTGGCCATTCCTA	84182
rs528886020	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30820529	TTTCTCCATTCCTCC[C/T]CCAACCCCCAGTCTC	84182
rs528905971	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30873605	GAGGGCGATTCTGCT[A/G]GTCCATGGACCACAC	84182
rs528986558	snp	C/G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771747	ACGAGGCGTTTCTGC[C/G/T]GTCGTCACCGGGCGC	84182
rs529021040	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30844280	GCTTAGTTATGGAGC[C/T]CGCTGAAAAAGCCTC	84182
rs529021663	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30879548	TTCCTCTCCCACCTC[A/G]GCCCGCACCACTCTC	84182
rs529095349	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30808406	CTTGGATTTCTTGAT[A/T]CTCTGATTTTGGTTT	84182
rs529115171	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30891386	ACCACAATTTAGTTA[C/T]ACTCCGTGCTTCTTC	84182
rs529123910	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30873743	GAGGAAGATTTTAGA[C/T]ACAGATCAGGGAGCA	84182
rs529152264	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30888104	TTTCCCCATGAAAAA[C/T]ACTGGGTCCATCAAC	84182
rs529155331	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30855638	CACCAGGACCTCTGC[A/G]TCCTTGTCTATGAGA	84182
rs529158864	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30770988	TTTCGGTGCCCAAGA[A/G]GCAGAATGCTGGGCT	84182
rs529164725	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850097	AGTCATTCCCGAGCA[C/T]TGCTGGCTGGGCCTC	84182
rs529248134	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30880962	ATCCCAGATCAAGAT[G/T]GGAGCTGCTCACCCA	84182
rs529248525	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30887584	TGAAGCGTGAGCCAG[C/T]GAGGACCATGGTTTC	84182
rs529269055	snp	C/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30804453	TGCCTCTTGCTTGTT[C/G]GAATGGTGTTGGGGA	84182
rs529313054	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30864687	ATATATATGGACATG[A/G]GGTATCCCCAAAAGG	84182
rs529322758	snp	G/T	0.000399281	0.0141238	downstream-variant-500B	FAM188B, INMT-FAM188B	GRCh38.p7	7:30892506	CCAGAGCCCTTGTGA[G/T]GCCCCAGGAGAATGG	84182
rs529350785	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30851685	CCCTGTTTTACAGAT[G/T]AGGAAACAGAAGCCC	84182
rs529362551	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30846086	CTCACTTCCACTTCC[C/G]CTCTGAAGTTGGGGA	84182
rs529392606	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778928	TTCCATGCCCTGCTT[A/G]TGTAAGAGTTTCCTT	84182
rs529407353	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30770128	TACTAAAAGTACAAA[C/T]ATTAGCTGGGCACGG	84182
rs529443099	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30856454	GGGGTCCCCTTGAGG[A/G]TGTTCCTAGGACTGG	84182
rs529497513	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30823310	GTTGTATTGGCATCT[A/G]CTGATGACCCTTTCC	84182
rs529531632	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30784609	CCTTAGAATACAAGC[C/T]CCGGCTGCTCCCCTG	84182
rs529566291	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791060	GAGGTGGGAAAAGAC[A/G]TTCCTGGGAGAGACA	84182
rs529615568	snp	G/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828900	CTCTCTCTGATTGAT[G/T]TCTTCTACTGCTTGC	84182
rs529617256	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30883488	CTGAACACTGAGCAG[C/T]GTGCCTCTGGCCTCA	84182
rs529634417	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30807328	CTGCCAAAGAAACCC[A/G]TCCACACACAGAATT	84182
rs529677637	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30889482	CCACCCCCAAATAGT[A/G]TCAGCAATGGGCACT	84182
rs529696626	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30812870	CATCGTGAGGCTCAA[C/T]ATGACATTTCCAACA	84182
rs529712562	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30769854	TAAGCACATAAAACC[A/C]AAGATCTTGTGGCTA	84182
rs529725117	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30812451	ACATGGAATAGACAG[A/G]AAAAATGAATAGCTA	84182
rs529780715	snp	G/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30819305	ATTTTCTAATGCATG[G/T]GTTATTTTGGGGGAG	84182
rs529783695	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30775137	ACACCAATTGGGTGT[C/T]GTACAATTCAAATCA	84182
rs529787879	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30781903	CTTAGTCAAAGAAGT[A/G]GAATAGTTGTCTTTT	84182
rs529793518	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853342	AGCTAATTCAGGATG[A/G]GGCACTGCGTGGGGC	84182
rs529794280	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30865568	CAGGGAACCAAATTC[G/T]GTCCTGTAGATCTCT	84182
rs529834387	snp	A/G	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30818612	TGAGATTCATAGCTG[A/G]GATGGGTGGTTCCAG	84182
rs529835263	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859781	TGGGTGGTGAATGGG[C/T]GGTGGCCAGGAGGCC	84182
rs529849905	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30829269	TTTCCTTCCACTCTT[C/T]AGTTTTGAAGCAAAC	84182
rs529852597	snp	C/T	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30864986	TCCCCTTGAGAATCA[C/T]GGGCTCTTGGAGGTT	84182
rs529886349	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30849803	CTCAAACTCAGTAAG[G/T]CTGAAGTGTGACTCT	84182
rs529890865	in-del	-/G	0.00478371	0.0486721	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30830643	AGCATGAGGGTAACC[-/G]CCCCCATGATTCAAT	84182
rs529892326	snp	A/G	0.0023933	0.0345097	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30826414	TGGAGCTGAGAAGAA[A/G]CTGATGTTCCACTTG	84182
rs529919753	snp	C/T			synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850505	CCTCGTCCTGGCCCT[C/T]GCAGACATTGTGTGG	84182
rs529952732	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30851233	ATACTCTGGGGGCAC[A/G]TTGGTCACTGTAGCA	84182
rs529957951	snp	C/T	0.000794912	0.0199204	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785787	TACTTGGTAATTTTG[C/T]ATCATCTAAAAGGCC	84182
rs529964119	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30871333	AGATAGCAGCTCCTT[C/T]CCTGTGTGCTCCTTA	84182
rs529991613	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30838300	TCTGGAGAAGACAGC[C/T]GTGAGAAAGTAGAGG	84182
rs530070590	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30860951	CACACATACACAAAG[A/G]CAAACATGGATACAC	84182
rs530100344	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30834043	CAGGCACATGGTGCA[A/G]GCTGTTGGTGAATCT	84182
rs530108026	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30789579	AGCCAGAAGTTTGAG[A/T]CTCCTCGGGAATGGT	84182
rs530211573	snp	C/T	1.65603e-05	0.00287747	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785929	GATGGGAGAGAATTC[C/T]AGGCCAAAGTCTGGT	84182
rs530218327	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30788937	GCACTTTATTCACCT[A/G]TTTTCATTGTGAGTG	84182
rs530223156	snp	C/G	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30891302	CAAGTGCTAGGAAAT[C/G]TCATGGTCTCACCTA	84182
rs530234495	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30833457	GCCACCTCCATGATT[C/T]GGTTATCTCCCACAG	84182
rs530293414	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30877380	GGGTCATCCTTCCCT[G/T]GTAATAAAATTGAAG	84182
rs530354785	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30807819	TTGCTCAGTTGATCA[C/T]GACCCTCTCACGCGG	84182
rs530377131	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30863699	ACTGCCTGCCTGGCC[A/G]CTTCATTGTCAGAGG	84182
rs530406390	snp	C/T	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30843437	TTGTCTCTAAACTCA[C/T]TTCAGCCTAGTGCTC	84182
rs530419219	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30842667	TACAGGGGACATGCA[C/T]GGTGCTAAGGGTTCA	84182
rs530420878	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30849232	ATTCTTCCTCCCCAG[C/T]ACAGTTCCGCATGGA	84182
rs530463466	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30830670	CAATTACCTCCCATC[A/G]GTTCCCTCCTATGAC	84182
rs530502937	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785707	TTTGTTACTGATTCC[G/T]TTTGGGGAGTCTGTT	84182
rs530520703	snp	A/G	4.99048e-05	0.00499499	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791207	CGGTCCTCACCGTCA[A/G]GCAGCTCCACCCAAC	84182
rs530534783	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30835490	CAGAAGCATTCTCAT[C/T]TAAGTTCAGGTTCAT	84182
rs530540795	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30863057	ACTGTCCCTGAGACC[C/T]CCCTTTGGAGAAGCC	84182
rs530593433	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785412	CTGGGCTTCGCATAC[C/T]GCATGACTGTACTGA	84182
rs530600570	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791978	GCTGCATGTGGGCTG[C/T]GGGTTGGACAAGCTT	84182
rs530633880	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30804338	AGTTTTGTGGTCATA[A/G]GTCCCTCAGAAGTGG	84182
rs530661291	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30867899	AGGCACACTTGTGCA[C/T]ATCCTAGGAGGCCCC	84182
rs530717908	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30874697	GAACTCATACTTGGG[C/G]TTCCTACTCCCACCT	84182
rs530743255	snp	C/T	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30803494	GATGGATGGTGCTAA[C/T]TGAGATGCCGTAGGA	84182
rs530748659	snp	A/C	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30797496	TGATCTCTGGACGCA[A/C]ATGCCGACAGCAGTT	84182
rs530807619	snp	C/T	0.00318978	0.0398085	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30793180	TATATATGTATTATT[C/T]TTTATGATTGCAATC	84182
rs530825691	snp	C/T	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30846163	ACATTGGTAGCAGAA[C/T]CTATGGTCCTGCAGC	84182
rs530827579	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30845731	TCTGGTGGGGAAATG[A/G]TTCTGTGAAAGCAGA	84182
rs530837796	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30851455	CAGTTTAAATCATTT[C/T]ATCAATATGAATAGC	84182
rs530846398	snp	C/T	1.6656e-05	0.00288578	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836651	CATGGCCATGGTTTT[C/T]TTTCAGAGGATGTGG	84182
rs530856158	in-del	-/AG	0.218151	0.247963	upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30770297	TCAAAAAAAAAAAAA[-/AG]AAAAAAGAAAAAAAA	84182
rs530880066	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30799996	TAGTCATTGGCTGTG[A/G]GCTGCCCATCCTGGA	84182
rs530913627	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30847209	TTTTTCCAACTCTAC[C/T]GTGTTTTCTAGAAAA	84182
rs530918704	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30781864	TGGCTGAAAGCTTGT[A/G]TGAATGAGTGAGAAG	84182
rs530924221	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30876605	GCCAGGTGCTGAGGG[G/T]GCTGGGCAGAGGAGC	84182
rs530972370	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852748	AATAATGGAAGACAT[A/T]CATTTTTGTATTTTG	84182
rs531056471	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30805700	TTGAGCAAAGTGCTC[C/T]GGGGCAGAAAGTCAA	84182
rs531125257	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30888160	CCACCCCTCTGTTGC[A/G]GTGATGCCTCTGGGG	84182
rs531139007	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30817546	ATGGAAGCGAGGAAG[G/T]AGTACAGCACCGCTG	84182
rs531147156	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30857864	AATTCCTGGATGACA[A/G]TAAAGAGTATATTTT	84182
rs531167676	snp	G/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30887641	CCACTCCCTAAGCAG[G/T]CGTCCAGGAGGAACA	84182
rs531318251	snp	A/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850070	AGGGCCAGGGCAGGG[A/T]CCTGAGATGGCAGTC	84182
rs531336707	snp	C/G			utr-variant-3-prime, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30892111	ATGTACCCCAACCTG[C/G]GTCAGCATGACTGCA	84182
rs531340888	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30878732	TGAAGGGACCCACAA[A/G]GGAAAACAGCTTGAC	84182
rs531348210	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30802164	CTGCTCTGTTAGCTA[C/T]GTTCCAGCAGTTCCT	84182
rs531362027	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839007	CAGAGGTAAGACCCT[C/T]ATTATTGAGTTTCTC	84182
rs531375465	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30855085	AACTGCTGATGCGGT[C/G]CATCCACCGCCTGGC	84182
rs531378095	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30851871	CAGTGAAAACAAAGG[A/G]CAAGTCAGCATTCCG	84182
rs531383256	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30777031	TTTTTTTTTTTAGAG[A/T]TAGGGTCTCACTCTT	84182
rs531390283	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853819	AGCAGCCGCCACTGG[A/C]ATACAGGAGCTCTTT	84182
rs531395323	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30814038	GGTCATCCATTTGGT[A/G]CAGTCAGTAAAATAA	84182
rs531433964	snp	A/G	0.0023933	0.0345097	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30811575	TCTGCTTCCAAAGAA[A/G]GAAGAAGTAAAAACT	84182
rs531434401	snp	A/G	0.00358779	0.0422022	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30844141	ACCGGCTGCTGCCCC[A/G]TCACAGAGGTGCTGT	84182
rs531459880	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30808319	ACCCATGGCATACCT[A/G]TACCGGCACTTTGGT	84182
rs531488109	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30854508	CTGAGACCCCCACTA[C/T]GAAGCAGAGGAAGAA	84182
rs531492931	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30860830	CTTCCCCCTCCCTAC[C/G]CTTTCCAATCAAGCT	84182
rs531497181	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30786831	GGTAGAATTCCATTA[A/G]GCAGAGAGACAAAAC	84182
rs531533612	snp	G/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30813456	TGGATTCTCAGCCAT[G/T]TCCAGCCCCTCAGTG	84182
rs531590103	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30809720	TCTAATCTTGTGGCC[G/T]TAGACAATCTAGTCC	84182
rs531594136	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	FAM188B, INMT-FAM188B	GRCh38.p7	7:30892430	ACAGCTGCAAAGAGC[A/G]TGATGTGCACTGTCT	84182
rs531602816	snp	A/G	0.0023933	0.0345097	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30820191	CAGGCGTGAGCCACC[A/G]CGCCCGGCCAATAAT	84182
rs531630292	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30772183	GGGGAAGGAGCTCGC[C/T]GGGGGGTCTTGGGCG	84182
rs531630671	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30813879	TTTGGGTGTAGGTCA[A/G]AATTTCCTGGAGGTT	84182
rs531639647	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782707	GACCCTGTCTCTTAA[A/G]AAAGAAAAAAAAAAG	84182
rs531645131	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30789342	GTTTTGGGAGGTGGT[A/G]TCTGAAACCCACAAA	84182
rs531687991	snp	C/G/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30856272	TGCAGGCGTGTTGCC[C/G/T]TGTGGCCTCCCATGT	84182
rs531701135	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850809	GGTCTGTCTGCCCTG[A/C]CTTCCTCCTGAGGAG	84182
rs531752697	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30862375	ATGTGGGAGTGCGCC[C/T]GTGAATAAGCCATTC	84182
rs531776180	snp	C/T	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30784178	GCTCTTCCTCCGAGG[C/T]ACTTACTACCTGGCT	84182
rs531791933	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771678	CCTACTGCCTGCTCC[A/G]GAGATGCCCCAGAAG	84182
rs531798706	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30815054	GTGCAGCTTACTTCC[C/T]TGACACGTTGGTTGG	84182
rs531803858	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30867803	CCCTAGTGGTCAGGT[A/G]GAGGGGGGATAGCTG	84182
rs531810840	snp	C/T	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30805509	TTGCAGTGGAGACCA[C/T]GTGCTTGGTGTGGGG	84182
rs531840689	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839864	TGCAGGCCTAGAACA[C/T]GGCTTATACCCAGTT	84182
rs531873541	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30855794	TGGACTCAAAGCAGT[C/T]GCCTCCTCGCCTGGC	84182
rs531885097	snp	A/G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30790436	AAACCTTTCATTTTC[A/G/T]GAGGTTTTGGGATTT	84182
rs531898961	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30841337	ATGAGCACCTTATTC[C/T]CATTCATTCAGCACA	84182
rs531909986	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30821900	TGTAAAAAGCTTGAA[A/G]GAAGAGTACAATGAA	84182
rs531910602	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30873505	CTTTGAATGAATCCC[C/G]TAGGGGTCTTGTTGA	84182
rs531914436	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30881035	ACTGGAAAAATAATT[C/T]CCATTCTTTCTTTAA	84182
rs531917371	snp	C/T	0.0023933	0.0345097	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30829303	TTTTCTCTCTCTTTC[C/T]GTAATTCCCTACTCT	84182
rs531964430	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30830824	GGTCTTGTCAAATAG[C/T]GATGTGGAAGGAGCC	84182
rs531972569	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30857990	CAAAAATGTAAACAT[G/T]GTAAGTTTTATAATT	84182
rs531977092	in-del	-/CTTT			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30822178	TTTCTTTCTTTCTTT[-/CTTT]TTTTTTTTTCTTTTG	84182
rs532006315	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30888710	GCTCAGCCCTTTCAA[G/T]TTTTAAAATGTCTCT	84182
rs532041634	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30789814	CTGTTTTTGTCTCCC[C/T]ACCCTCCCATTAATA	84182
rs532057139	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30834126	GGTGCCCCCGTAGGG[A/G]TTCTTTGTGGAGCCT	84182
rs532073456	snp	A/G	0	0	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30817792	CCATCCACTTCCTAT[A/G]TGTCTGTCCATGTCT	84182
rs532109396	snp	A/C	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30775052	TCTCTGATAGTGTTT[A/C]TGCTCACACTTCAGA	84182
rs532110735	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30780228	AGCAGATGCTCTGCA[A/G]TCCTCCGTCTGCTGT	84182
rs532131985	snp	C/T	0	0	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30871219	GCCCCCCAGAGCCAG[C/T]TTCTCTGTGCTTCTT	84182
rs532162659	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30786450	AGACACTTGTCCCAC[C/T]GCCCCATCTCTACAA	84182
rs532168241	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30864249	CAGGACCCACGCCAT[A/G]TCACTCTGTGGCTCT	84182
rs532188428	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30825034	CCTTAGCAGAGGGTC[A/G]AGCCGAGTTCTGCCA	84182
rs532199720	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30825795	TGCTTATAACTGTTA[A/C]CATGTGTATTAGTTT	84182
rs532207261	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872862	TTTTCAAGATGTTAC[C/G]TAGTGAGCATCAAAA	84182
rs532221164	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859378	GGTCTGTCTTGTTCA[C/T]TGCTGCCTCGCTAGA	84182
rs532266952	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30851780	GCTCCGATTCCTGGA[C/T]GTCTTGGGCTACACA	84182
rs532279149	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30864795	AGGAGAGCAGATGTG[A/G]GTTTGGGGTGGGCTG	84182
rs532323709	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30832065	GGTCCTAAACCAACT[C/G]CCTGCACTTGGGCCA	84182
rs532413272	snp	A/G	0.00795532	0.062565	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30833371	AGAGCCTGTGTAGGC[A/G]AGCTTCTGTTTTTAA	84182
rs532417146	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30865803	TTAATGGCACAGTTG[A/G]CAGCATCACCTGAGG	84182
rs532422899	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30832798	CAGGCATGAGCCACC[A/G]TGCCTGGCCCCCTTC	84182
rs532426557	snp	A/C	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30795002	AATTTTTACTTACAA[A/C]CCCCCAGGGCTAGGT	84182
rs532435939	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30835781	CTGCTCAGCCTTGCC[C/G]GCACCATTGCCTTGG	84182
rs532439185	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30826662	AAGCAGTAAATGTAG[C/T]TATTGCCCTTGTCTT	84182
rs532454061	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30841524	GGTGGGGCTGGAGGC[A/G]AGGCCTTCTTGAGGA	84182
rs532465304	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836112	TGATAATTACTTTCT[C/T]ATAAGGCTGTTGTGG	84182
rs532471202	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30870243	GAGGTAATGATCTTA[C/T]GAAGATTGGACTGCT	84182
rs532496345	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30866520	AGACCAGTTCTAGCC[C/T]TCAAAGTCCTTGCCA	84182
rs532539595	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30788799	ATCCTCCACGGTCAG[C/T]GGAATGCCTGCCGTG	84182
rs532618908	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30783677	TTTTCAAAATCTCTG[C/T]TGTGAAGTGCTGTTA	84182
rs532626335	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30788358	TGTCTTGCACTTTGA[A/G]GTTTTTACCCCTGAA	84182
rs532654490	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30837985	AAAGGAAAAAAAGAG[C/T]TGATTCTGGTGGAAA	84182
rs532662751	snp	A/C	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882877	ACCTCAGGGTGAGTG[A/C]AGGGCCCTGGGTGAC	84182
rs532679891	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840583	GGGTCTTGTCACTCC[C/T]TCTCTGTGGCCCAAG	84182
rs532682770	snp	G/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872001	AGCCCTGGTGCGGCT[G/T]GAGTGGAGGCCATTG	84182
rs532685038	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30842237	TGTTCTTCTCTCTGC[C/T]TCCCCTCCCCTTTGC	84182
rs532686617	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30877814	GTAGCTGGGATTACA[A/G]GGACATGCTTTTTTT	84182
rs532689846	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30857657	TTTTGTATTTTTAGT[A/G]GAGACGGGGTCTCGA	84182
rs532704888	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852969	AGGAGACTCCTAAGG[A/G]CTGCTTCCTGCTGAA	84182
rs532714044	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30837486	ATCAAAGAGCAAAAT[A/G]TTTTTCTAGAGGTTT	84182
rs532746055	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30877321	TCAGAGAGTAAACTA[C/T]TTTCCTGTGGTCTGT	84182
rs532746531	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30883427	AGGTGCTGCCTGGAG[C/T]GACACCCTCTGCTTG	84182
rs532749517	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30869344	ACACTGCCTTCAGCC[C/T]GTATGTTTCATGTAA	84182
rs532776545	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30842616	GCCCTCATGGCACCT[A/G]TGATTGAACAGGAGA	84182
rs532818317	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840689	GGTGGGTTCTGGGGT[A/G]GGTTTGGGTGAAACC	84182
rs532821560	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30814763	CATGAGCTCCAAAAA[G/T]AAGTGTTATTTAAGT	84182
rs532881431	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840310	GAGAGCGCAGAGCTC[A/G]TGTAACCACAGGCTG	84182
rs532901134	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30862477	GCGCTCCCTGCATCC[C/T]GGCACCTCCAGCCTT	84182
rs532921749	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30822678	GGTTTCACTCTTGCT[A/G]GGCTGGAGTGCAGTG	84182
rs532940143	snp	A/G	0.0023933	0.0345097	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30873150	TGGTTTGTCCAGGGC[A/G]CCCACAGAGGGACCG	84182
rs532947961	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30784649	TGCCTTAGAGGCCTG[C/T]GTGCTGGGGCTGGGC	84182
rs532961950	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30868892	GGGTTCTGACCCTTC[A/G]CTGCCAGAATGCTGC	84182
rs532965883	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30797820	TTAGGCAACTGCAGT[A/G]GTAGAAGAGAGCTGG	84182
rs532969596	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30809630	CAAAGGATAATTAAA[A/G]TCCCAAACTTACAAG	84182
rs532976623	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30874597	AGGGTTGGCATGCTT[A/G]TTGGCTTGCCAGGTG	84182
rs532979310	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30803360	GCTTGGAATTTGGAA[A/G]GGGAGAATGAAGTAT	84182
rs532984431	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30829473	ACCATTTGGGCAGAC[A/G]AGAGCTGTTCACATG	84182
rs532984620	snp	C/T	8.49307e-05	0.00651599	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791183	TCTTTTCACAGACAC[C/T]ATCTGAGACGGTCCT	84182
rs533034145	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30891818	GTGTGAATTTGGAGG[A/G]GTGAGATGAGCAGGA	84182
rs533072767	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850765	CTGCGATGCCCTCTC[G/T]GGGCTCCAGTTCTCA	84182
rs533075280	snp	C/T	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836369	CACTCTATGTCCATG[C/T]GTGGAACTTTCTAGT	84182
rs533091962	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30874187	CAGCTGTGGCAGAAG[A/G]TGGATGAGACAGAGA	84182
rs533149498	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30796812	ATGTCACTAACCAAC[A/G]TATGATGTCTTGCTC	84182
rs533163338	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30881748	TGTCCAACGGTAAGC[A/C]AGCTCTAGGCTAGTG	84182
rs533168449	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30879669	TCGTTTTGACTTAAA[C/T]GTTACTTCCTAAAAG	84182
rs533170957	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30774869	CTTCTCTTCTTCTTT[C/G]CGTTCACTCTCAAGA	84182
rs533172713	snp	G/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30798692	TTTAGTAGAGACGGG[G/T]TTTCACCATGTCAGC	84182
rs533207893	in-del	-/T	0.0023933	0.0345097	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30821955	CAGCAATTGGTATGA[-/T]TTTTGTCACATTTGT	84182
rs533216865	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30772044	AACAGTGGGAATTCC[A/T]GTGGTTGCTTTAATT	84182
rs533238541	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30887621	GAGTGCCTGGGAGGG[C/T]GGGGCCACTCCCTAA	84182
rs533251948	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30845176	GCTGGACACCCACAC[A/G]GACTCCTAGGGACCA	84182
rs533259256	snp	A/G	1.65638e-05	0.00287778	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852251	TCAGTCCAACAGGGA[A/G]ATACAAAGCAGATGG	84182
rs533267061	snp	A/G	4.32947e-05	0.00465247	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850494	CGGACCCGCTGCCTC[A/G]TCCTGGCCCTCGCAG	84182
rs533307794	snp	G/T	0.00398564	0.0444627	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771617	GGGGGATCATCGGGG[G/T]CTCCCCTGAAGGCTT	84182
rs533355613	snp	C/T	0.00028278	0.0118874	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882277	CAGCCGGGGCTCCTG[C/T]GTGACTGGAGGACTG	84182
rs533360486	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30805569	GAGCCCCACCCAAGG[C/T]GAGGGAAGAGCCAGT	84182
rs533397756	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30847184	CCTCTTACCTGTCTG[A/G]TCACTGTACTTTTTC	84182
rs533399564	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30797421	GAGGTAGCCAGGAAA[A/T]CCTACCAGAGAGGGT	84182
rs533422316	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30779010	AGGTAGAGGAGGGAA[C/T]TGGGTTCAGCTAACC	84182
rs533423721	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30842054	TCACCAGCACGGATG[A/G]TTTTTCCTTAGTTAG	84182
rs533423773	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30862549	GATTCGCAGGGCAAT[C/G]ATAACAGTTCTGGGG	84182
rs533432715	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30857134	AAAAGTAAATGATGT[C/T]CTCAGGGCTCTGCTG	84182
rs533469058	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30798642	GCTGGGACTGCAGTC[A/G]CCCGCCACCACGCCT	84182
rs533484766	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30843582	GGCACAAGGCAGACT[C/T]GGTTTTTGTTACCCC	84182
rs533492768	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30804527	CATCCCGACAAATAT[A/G]TACTACAGGATTAAG	84182
rs533496174	snp	G/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30788151	ATATGGTGTTTTGGT[G/T]GAAGTGTATGAAGAA	84182
rs533496454	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30794554	TGCTGAGATGTTAGG[C/T]GGTGTGAGTATCTGT	84182
rs533511620	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30773980	TCTGACAGTAAAATT[C/G]CACTCGTCCTGCTCT	84182
rs533550117	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30816875	AAGAGGAAAGAAAAG[A/G]CAGAGAGAAAAAAAT	84182
rs533550939	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30887049	AGATGTTTCTGTTCG[A/G]AGGTGCAGACAAGAA	84182
rs533561357	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30871654	ACAGTGGTACCAGGG[A/G]GTGGGGGCACAGGCC	84182
rs533563298	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30801027	GGGAGAGAGACAAGT[A/G]CATCCCAAACTCTCC	84182
rs533568764	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30816149	ACTCCTCAGCTTCCA[G/T]AGGGAGCATCCATTG	84182
rs533576324	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30824057	AAATATATAGCAAAT[A/G]TCTTAGTCTGTTTTC	84182
rs533605267	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785071	TCACTGTCTCTTGCC[G/T]TCTTTTTTTTTTTTT	84182
rs533605694	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	FAM188B, INMT-FAM188B	GRCh38.p7	7:30892628	ATAGGACAGGGATAA[A/G]CAGAGGGACTGGGGA	84182
rs533664051	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30863499	GTGATGTGTGATGGA[C/G]AGGGCATAGTCGTTC	84182
rs533684215	snp	C/G/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30880505	GCTGCACTTTTGTCT[C/G/T]TCCGTTGGAAAATTC	84182
rs533721415	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30883086	GCAGGAAGGCAGATA[A/G]GTTCCTGGACCACCC	84182
rs533733147	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30823815	CATATTTTAGTAGGA[A/C]TTAAAAAAACAAATA	84182
rs533746546	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30834044	AGGCACATGGTGCAA[A/G]CTGTTGGTGAATCTA	84182
rs533766052	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30838453	TACTAGACCAGGAGT[C/T]GGCAGGTGTTTTCTG	84182
rs533771433	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791740	ATGGTCAACCAGGAA[G/T]AAAACTCAGCCAGAG	84182
rs533814528	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30888370	CTAAACATTTCATAA[C/T]GCACACCACGGTCTC	84182
rs533825132	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30811935	TAAAGCCCTTCCTTC[C/T]TTAACTCAATGTCTG	84182
rs533830185	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30847752	TTTGTTTTTGTTTTT[A/G]TTTTAGAGACAGGGT	84182
rs533841314	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30774751	CTGTCCCTCTTAGCT[G/T]TCCTCCTACTCCTCT	84182
rs533859930	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30800589	GGCCCTCACAAAGGA[A/G]TGGAAGTTCAGGGAG	84182
rs533868515	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30842739	GACATTTTCATCTTA[C/T]GGAGATAGGAAGGAT	84182
rs533887366	snp	A/C	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853129	CTGTTGGGGCCACAC[A/C]GGATGCTGGAATTCT	84182
rs533891283	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30786996	CCACCTGCGCTCTCA[C/G]TTACCTGCTGTATGT	84182
rs533912534	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850115	CTGGCTGGGCCTCCC[A/C]GTCCCTGCCAGAACT	84182
rs533922906	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30884892	CACGGGCCTGAACCT[C/T]CTCTTCCTCTTCTAT	84182
rs533925075	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30854829	TACCCTAGGAACAAA[A/G]GGAGGCAGGTGAGGT	84182
rs533987127	snp	C/T	3.35847e-05	0.00409771	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836625	CTCCGTGAGTCATAA[C/T]GAAGGGCTCACATGG	84182
rs534022161	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30888860	CCAAGCTCAAACTCA[A/G]CAGCCTGATAGTAAG	84182
rs534039960	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30818675	TGGGGAGATTTTCTT[A/G]TATTTGGTGGAACAC	84182
rs534040016	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30811976	TCTGTGGCTTGTCCT[A/G]CTACAGTCCATTTAA	84182
rs534050561	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30815651	GTGTGTTCCAGAGAC[A/G]TGCTTCATAGAGATC	84182
rs534075346	snp	A/G/T	0.000354317	0.0133062	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853378	CCACTCATCCTGAGT[A/G/T]TTTGTGTCTTCTCAG	84182
rs534088196	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30818295	TCTCTCAAACTCATG[G/T]CTGATACAGTTGTCT	84182
rs534110862	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30884238	CACATGGTGGAAACA[C/T]CAGGAAGGGGAAATG	84182
rs534155205	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30779448	GCTGTGTGGTTGGGC[A/C]TAGTGTCAGAGTCAA	84182
rs534168907	snp	C/G/T	0.00517822	0.0506191	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30843762	TCTATCTGTCGTTGC[C/G/T]GGCCAGGCAGGTACC	84182
rs534237174	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30788504	CATTCATTGATGTCA[A/C]CCCCAGCTCATCCAA	84182
rs534259089	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30838333	CTGCCTTGAGAGGTG[C/G]TGGGAACCCCTTCAC	84182
rs534267445	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30890236	AAGGTACAATTCAGC[A/G]TTCCTATTTGGACAA	84182
rs534293761	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30770054	GGAGGCCGAGGTGGG[C/T]GGACTGCCTGAGGTC	84182
rs534309034	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30804856	GCTGGCATTAGCAAG[G/T]ACATAGAGGGCAGGT	84182
rs534351665	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30854129	GAGGGGCTACACACT[C/T]CAGGGGTAAAGAACA	84182
rs534352013	in-del	-/AAAAGCCCAG			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771981	CCCAGAGGGAACCCC[-/AAAAGCCCAG]AAAAGTTCTTGACGG	84182
rs534385958	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30885478	GATCATGCCATTGCA[C/T]GCCAGCCTGGGCAAC	84182
rs534386946	snp	A/T	0.000798403	0.0199641	downstream-variant-500B	FAM188B, INMT-FAM188B	GRCh38.p7	7:30892830	TGTTCCATTCATTGA[A/T]ATCCCACCAGTTTCA	84182
rs534393814	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30776044	CACTTCTGTTGCAAA[A/C]ACCTTGCTCCAAGCC	84182
rs534398261	in-del	-/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30793052	TCCCATCGTGGTTTC[-/T]TTTTTTTTTTTAACC	84182
rs534412208	in-del	-/GAGATAATATTTGG	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30802052	AAGTTGTTGGGCTCT[-/GAGATAATATTTGG]GAGATGAGTGTGAGA	84182
rs534429890	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782279	ATTACTATGTACTTC[A/G]TGGCTGTTTCAGTCA	84182
rs534540866	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30865907	TCAGCTGTGTCTGCT[A/G]ACTTAGAAAGAGAGG	84182
rs534545565	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30784838	AATCACAGCACACAC[A/G]ACTGCCCCTCCCACA	84182
rs534580642	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852383	GACAGGCTGGCCTTC[C/T]GCAGCCCAGGTCCCA	84182
rs534584961	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30887784	GTGCTGACGGGGACC[C/T]GCGGGTGGCAGTCAG	84182
rs534646220	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30869024	AAATCCCAGCAAGCT[C/T]TGCTCCCTGGAGGGG	84182
rs534656787	snp	C/G	0.000115949	0.00761321	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859025	GAGGTCACTGATGCT[C/G]TCTTTGGTGGCCCCT	84182
rs534672774	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30773582	CATGATAGTCTCCTG[A/G]AGATGGCAGGGTCTG	84182
rs534712868	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30772754	ATTGACCTGCCATCA[C/T]CTGTCCTGGCTGCAT	84182
rs534715649	snp	A/G	0.0023933	0.0345097	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30864489	CCAGACATTGTCTTT[A/G]GGAATTGGTGTCTGT	84182
rs534724480	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30838728	GGGAATCTTAAAACT[A/G]CTGATACTGGAGTCT	84182
rs534767342	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30856786	GAGACCAAGAGCTTC[A/G]TGACTTCCCTAGGCA	84182
rs534767579	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30863160	CATTCAGCTTTGCCA[A/G]AGAATCCTCTGATGC	84182
rs534803435	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778678	ACACTTGCGGTCAGA[A/G]AGAAACGGACCCCCC	84182
rs534824745	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30831113	TGTTGGGATACTGGT[G/T]AGGGGCTCTTGGCAT	84182
rs534849553	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30830340	CAGATGCCCAGCAGT[A/G]CTTAAGTGCTTTAAT	84182
rs534873333	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30889448	ACCTATATTAGCCAG[C/T]ATAGGACATCATCAG	84182
rs534880509	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30822358	GTATTTTTAGTAGAG[A/C]CAGGGTTTTGCCATG	84182
rs534889616	in-del	-/AGAA	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30809023	CAGAAAATCAAAGAG[-/AGAA]AGAAAGAAAGAGAGA	84182
rs534924147	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30779569	GAAGGGAAAATGCCC[C/T]ATTTGAAGTGGGGAA	84182
rs534960910	snp	A/G			downstream-variant-500B	FAM188B, INMT-FAM188B	GRCh38.p7	7:30892856	TTTCAAAAAGAAGAT[A/G]AGAACATGCAGAAGT	84182
rs534979980	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30841162	TCCACCCACCAGGTC[A/G]ACCTGCCGACCTTTC	84182
rs534992178	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30841010	ACAAGGCCTGCGCAG[A/G]CCAGTGTTAAGGGGA	84182
rs535043836	snp	G/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30861268	TAAGACGACAGTGTG[G/T]AGGCAGGTCTCATTG	84182
rs535047900	snp	A/G	0.00398564	0.0444627	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30786822	GGTGACCATGGTAGA[A/G]TTCCATTAGGCAGAG	84182
rs535097266	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30783664	CCCACGCTTTGTGTT[C/T]TCAAAATCTCTGCTG	84182
rs535113217	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30831732	GCTCCCAGAAAAAAG[C/T]TGTGTGGCCCATTCT	84182
rs535155580	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30871085	GGGCTGCATGTGACC[A/G]CCAGGTTCAGTTGTG	84182
rs535181358	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30792563	TCAAATTTCAACTTT[A/C]TTCTTGTGTAAGTTT	84182
rs535185644	in-del	-/ATA	0.0023933	0.0345097	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30817974	TGCCCTCTAGTATGT[-/ATA]TCACCAGCATATTGG	84182
rs535195156	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30834188	AGCAGAGGTTCTCCA[C/T]GAGGGCCCCGCCCCT	84182
rs535218444	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30876119	TGTCAGAAAGGCCAT[C/G]CTCCCTCTGAAACCC	84182
rs535224245	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30879914	TCAGACTTTGACACA[C/T]CTGCTTTTTCTTACT	84182
rs535232646	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30873137	AGCTTGGGGCCTGTG[A/G]TTTGTCCAGGGCACC	84182
rs535240855	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30798761	CCTCGGCCTCTCAAA[A/G]TGCTGGGATTACAGG	84182
rs535262330	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30871729	TGGTTTTCTCAAAGG[A/G]TTTTAGGGAATAATG	84182
rs535307077	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30881859	ATCTCAGGAGGAAAG[A/G]CTGGCAGTGGGGGAG	84182
rs535307277	snp	A/C	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30866734	CTGGTGGGGGTTTGC[A/C]GGGATCAGTTGCAGA	84182
rs535343982	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30843752	AGTGAGGTTTTCTAT[C/T]TGTCGTTGCCGGCCA	84182
rs535352366	in-del	-/G	0.00398564	0.0444627	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30861131	ATGGTCAAGGCCCCT[-/G]GGGGCAGTACAGGCC	84182
rs535403078	snp	G/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30842997	TCCACTGCCAGCTGG[G/T]GCTCTTGCTCATCGA	84182
rs535467407	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30880503	AAGCTGCACTTTTGT[C/T]TCTCCGTTGGAAAAT	84182
rs535475014	snp	A/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828404	CATGCAGTGCTTGGC[A/T]AACGCCAACCTACAG	84182
rs535481289	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30874321	CATGAAAGTAACAGG[A/G]TTGGGGGAAGAGGGA	84182
rs535523983	in-del	-/CTT	0.00358779	0.0422022	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771961	CCCACTCGGAAAGAA[-/CTT]CTCCCAGAGGGAACC	84182
rs535526650	snp	A/C	0.0475351	0.146656	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30802947	CCCAACCAACCAACC[A/C]ACCCAACCAACCAAC	84182
rs535528167	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30886412	CTTAAACCCAGCTCT[G/T]TTGCCCTGCAAGAAC	84182
rs535539476	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30827498	TCTAACCACCCCTCT[A/G]TGCCTTAACTCCTCT	84182
rs535547350	snp	A/G	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30784776	TCTGCCTGACATGCC[A/G]CAATCACAAGGCTGG	84182
rs535610000	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30838566	ACACAGCCATGGGTG[A/G]TATGGAAACAAATGG	84182
rs535628425	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882038	CAGTGGCCTGAGCAG[C/T]GTGAGGGGCTCCCAG	84182
rs535639989	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30795344	AGAGTTTTATCCTCC[C/T]TTAGGAATTCAACCC	84182
rs535687612	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30855938	GCCCTCACCAAATTC[A/G]TTTTTCATGGCCTGG	84182
rs535715581	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30891215	TAGTGCCAGATTTTA[C/T]GTAAACACTCCATCT	84182
rs535719474	snp	A/C	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778058	TTACATTGGGCAAGT[A/C]AACCCCATCTCCTGG	84182
rs535750775	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30777456	CTGACCCATATATCC[A/C]TTTCTTTCCATTTCC	84182
rs535774640	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30861853	CAGGGATGTCCGGCA[A/G]TTCCTGATGGGGCTT	84182
rs535810693	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30834875	ACAAGAGTCACCTTT[A/G]CTCCAATTCCCAACA	84182
rs535825926	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30818707	TCAGTAAAACTCTTC[A/G]TGTATATGTTGGGGC	84182
rs535828414	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30793602	TATTTTGTATTTTTT[C/G]TAGAGACGGGGTTTT	84182
rs535837324	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30800542	AGCCCAGGGTGCACT[G/T]GGATGCCCTGTGTAA	84182
rs535851708	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30803551	TGGATGAAGCAGGGC[A/T]AAGCTGAGCCTTGAA	84182
rs535853265	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30806688	GCAGGCTTTTGGAAA[C/T]GTTTGTGGATTGAAT	84182
rs535854321	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30873818	TTGCCTGAAAAAGGC[C/T]GTGCCTTTCTCAGCA	84182
rs535870442	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30866495	GTTGCTGTGCACCTG[C/T]GGGGTCTGGAGACCA	84182
rs535881399	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30876289	CCCTTTGTGTCTTTT[C/T]TTATACAGACCTCAG	84182
rs535895150	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30888749	TTTCTATTGTAATTG[C/G]AAACTGCTTCCCTCT	84182
rs535932163	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30846662	GTTCTCACGCAGGCA[C/T]ATACAGCCCTGGCTA	84182
rs535935123	snp	A/G	0	0	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839977	AGTTTCTTAAGCCCC[A/G]GGAACCTCCCCTGCC	84182
rs535941742	snp	C/G	0.00676609	0.0577691	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882550	GGCGGCCAGAGCTGG[C/G]CCTTGAGCAGTGAGT	84182
rs535963162	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30772521	TAATATTAACATATG[A/G]GCAGCTTCCAAGCAT	84182
rs535997183	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30845423	TTGATTGTGTTATTG[A/T]TGTTCCTTCAAAAGC	84182
rs536026737	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30888332	GAGGACATTTTTAGT[G/T]GTCACAGCCCTGGGA	84182
rs536083512	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30800700	ACCAGTAACATTGGA[C/G]AAGGAATGGCTGTAC	84182
rs536095104	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30808775	GACCAGTTCCTGTAC[A/G]TAGACACTTGGTTAC	84182
rs536100651	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30815216	TCAGGCAGCCTGTCA[A/G]AACCTTCCCTTTTGT	84182
rs536104147	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30811347	AGCTCCCTTGTTTGC[C/T]ACCTATACTTCTTCA	84182
rs536111939	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30774287	ACCTTCCTGGGCTGC[A/G]CCATTCACTCTGCTC	84182
rs536125153	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30874532	GGAGGCATGGGTTGC[A/C]GGTGACTGCTGGAGG	84182
rs536189237	snp	C/T	6.92413e-05	0.00588352	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791563	GCAGGGCAGCCAGCC[C/T]GCACCTGTCAGGTGA	84182
rs536190326	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30855484	CCAGCTGAAGCAGAA[C/T]GTGGAGCCACCAGAG	84182
rs536201877	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30849033	GCCAGTTTATGGATG[A/G]GGAAACTGAGGGGCC	84182
rs536220472	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30876833	TCCTCAGAACCAGGA[C/T]GCAGAGATTGACTCA	84182
rs536232687	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30863858	CGGTAAATCTCATGC[A/G]GGATTTCATGCTTGC	84182
rs536242398	snp	A/G			downstream-variant-500B	FAM188B, INMT-FAM188B	GRCh38.p7	7:30892617	ATGGGGGGACAATAG[A/G]ACAGGGATAAACAGA	84182
rs536243885	in-del	-/GGGAGGAAGAACCCTCCTGA	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30844498	GGTAGATAGGGGTTG[-/GGGAGGAAGAACCCTCCTGA]GGACAGGTTAGGGCT	84182
rs536283558	snp	A/G	0.000165739	0.00910175	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882956	GAGGACACAGACAAC[A/G]ACCTTGTCCCACCCC	84182
rs536307955	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30819767	ACTTTTTATCCCAAA[A/G]TCTGTTTTTATCTGA	84182
rs536337670	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30841866	CTTAATCTTGCCAGT[G/T]CCTGAACTTTATTGA	84182
rs536400716	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853069	CACCTCCCTGCCAGC[A/C]GCCTCTCTGATATCA	84182
rs536430610	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30871962	CCGTGTCACGCTTCA[A/G]TCGCTGTTCTCTAGT	84182
rs536438480	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859585	GCCCTTGAGGAGCTT[A/G]CCTGGAACTGCAGTG	84182
rs536442542	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30788424	ATATTGGTTAGTGAG[C/T]TATATAGATCTTCCA	84182
rs536465615	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30858875	GAGCCTCAGTTCCAC[A/G]TATGCTAGAGGGCAG	84182
rs536481004	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30832906	CTTATACTCTTATTA[A/C]CTTCCTTTCCCATAA	84182
rs536485899	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30826228	GGGATTAGGATGTGG[A/G]TATAATTGAGGGCCG	84182
rs536493355	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850667	TACCCACCCTGTGCC[A/G]CATGCTGGGATGAGC	84182
rs536493503	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30817859	GTTCATTGCAAAATG[A/G]TGTTCTGTTTCACGT	84182
rs536511251	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30825158	GATTTATCTTTTTGT[C/T]ATTGTTGTTCAGAAT	84182
rs536630473	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30772558	TGACATATAGATACA[A/G]TGTGCACGTAGGTGT	84182
rs536633397	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30883841	GCTCTGGAGAGAAGT[C/T]GCCTGGGTTCCAGCC	84182
rs536635721	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30770015	CCGGGTGCGGTGGCT[C/T]ACGCCTGTAATCCCA	84182
rs536646376	in-del	-/T	0.00953873	0.0683987	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30858123	TGTCTTCAGTCACAG[-/T]TCATGGTTTCCAAAG	84182
rs536647272	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30888813	GTTGGCTGGATGGAG[A/C]GGGTTGGTTATGTCT	84182
rs536672139	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30889672	CTTGACACACAGAAG[A/C]CCAGTAAATAGTCTG	84182
rs536695605	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30813109	GAGAACCAAGGACAC[A/G]GGATTTTGGAGGGGG	84182
rs536708792	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30822811	TGGCTAATTTTTGAA[C/T]TTTTTTTTTTTTTGC	84182
rs536720181	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30878359	GATGACCCATACTCA[C/G]GGTGTACCTGGGGTA	84182
rs536764492	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30779998	AACTAAAAACAACTG[A/G]CACCTACAGGAGCAC	84182
rs536771947	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30829655	GTGGGGGTTTGTTTA[C/T]TCTGCCTAACTGATC	84182
rs536777667	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30862594	CTGCCTGCTGCCTCC[A/G]GGGCTAGCCGCTGGC	84182
rs536781678	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30860133	TTGAGGGATGCAGGT[C/G]GGGTAGGACTTGGGA	84182
rs536829796	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30844690	GGTGGGTGTCTAGCC[C/T]GTAGATGTTGGTGCC	84182
rs536830521	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30865846	AATCGAAGACCCTGT[A/G]CCTGCATCGTCTTCC	84182
rs536840199	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872094	GGGAGCCTCCTCCGT[A/G]GAGGGCACAGAACAG	84182
rs536842005	snp	C/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30865243	GGGTTGGGTAAGTGT[C/G]CTTCCTACCCAGCAT	84182
rs536882577	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30788099	TAGTAGAAGACAATT[A/C]AAGCCTCATATTTGC	84182
rs536901631	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30826486	TAGATGGAATGAGCA[C/G]CTTATGAAAAGATAT	84182
rs536912015	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30871610	TTCACCTTGCATCTT[C/T]TGAAGGACTCCATTC	84182
rs536914840	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852066	TGGGTGAGTTCAAAG[A/T]GGGGAAAAATGAGAA	84182
rs536950285	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30832431	AATTAATCACACATC[C/T]CTTTTCCTCCAGAGA	84182
rs536957823	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839741	TTAATGAAGGGGAGG[C/T]GGTTTGAAAGTCTAG	84182
rs536970706	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30794101	GCGAGGCGTCTTTGT[A/G]TAGTGCACATACTAC	84182
rs537004524	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30857258	GTCCCTTAGGTTTCT[A/G]TTCAGACATCGCTTT	84182
rs537040445	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30863903	TTTCAAACCACATGG[C/T]TAGAACTTTCCCCAG	84182
rs537073952	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30841035	AGGGGACTTGTGCGC[A/G]TTTGTTTCTGAAAGC	84182
rs537112290	snp	G/T	0.0023933	0.0345097	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778644	TGACAGGAGAGGCTT[G/T]AGGTTCTCCTGGCCT	84182
rs537149806	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30873862	ACGTGCATTATTTTA[C/T]AGCAGACATTTCCTC	84182
rs537168510	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791676	ACTTCTTAGTCTCCT[C/T]GGTCTCTCAGAACAA	84182
rs537172749	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30822066	TCATTCTAAAGTAAA[A/G]TACAGATATCCTGAC	84182
rs537225499	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30874885	TATGTAAGATGTTAT[C/T]GTTGGGGGAAGCTGG	84182
rs537238522	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30784393	CTTTCTCTGCCCACC[A/G]GCGAGGGCCTCAGTT	84182
rs537243562	snp	A/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30862181	GAGGGCCTGCAGGAG[A/T]TGTGGGCATCTGAGT	84182
rs537244201	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30868165	AAGGGACAAGCTGTG[C/T]CTGAGCCAGCAATGG	84182
rs537244446	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30874225	CTGCCCTAGTGCTGG[A/G]GCTGGGCTCGCTCAA	84182
rs537287572	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30835087	GATATCTTTTCAGCA[C/G]CGCCCCACTTTACTG	84182
rs537350484	in-del	-/T	0.308661	0.24302	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30812281	GTTGAGGGGGGGGGG[-/T]GTATGTATGTATGCA	84182
rs537444451	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30789167	GACTACTCTGAGGAC[C/T]GGTGAACCAGAGAGG	84182
rs537448963	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30866189	CTGAAGAGCTGGGAG[G/T]TCTCAAGACCCTCGG	84182
rs537452599	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872723	TATTGTCTTTATAGC[C/T]ACCCTTCCCTTTGCA	84182
rs537458876	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30795319	GTGTAACTGTGGTCA[C/T]GAATTGAGAAGAGTT	84182
rs537485922	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30792417	GGTCCCTCTTTTTCT[A/G]TCCCCTTGAAGAGTG	84182
rs537495685	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30806899	CATGTGGCTGTGGTC[C/T]TCCATGTCCCTGCTT	84182
rs537510215	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30878111	GGACCTGGACTCAGA[A/G]CCAGGGCCCTTGCTC	84182
rs537532434	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30838531	TGCTGCACCTATTCA[A/G]CTTTGCCATCATGGT	84182
rs537539953	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30780255	CTGTATTCTAAGGCA[A/G]GAGAGTGGACTGTAC	84182
rs537541709	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30830469	TTGACTCACAGTTCA[A/G]CATGGCTGGGGAGGC	84182
rs537570795	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30801680	CTGAGCCCTCCAAAA[A/G]TGGGGTTGATGACCC	84182
rs537603927	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782362	TGTGTGTGTGTGTGT[A/G]TGTGTGTGTGCATGT	84182
rs537626847	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30881794	TTTGAGGGGTGTGGG[A/T]AGAATTGGTTAGGAG	84182
rs537635074	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30798161	CAGCATGTTGCCGTA[C/T]TGAATGCTATAGGCC	84182
rs537647660	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30804661	CTGACTGGCCCTCTT[A/G]TAGGAGCTTTGGATG	84182
rs537702341	snp	G/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30883173	GGGGCCCAGGTTCAG[G/T]AGTGTGTGGTCTGCA	84182
rs537707534	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30803787	AGCGTGTTTTTCTAC[A/G]GCCTGCATTGGGTTT	84182
rs537708432	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30769966	GTATAGGGGTTAAGG[A/G]CTGAATTGTGTCTTT	84182
rs537709165	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30848311	GGTGATTGGACGGTG[C/G]GGTGAGATGGAGCAA	84182
rs537717030	snp	A/G	0.0023933	0.0345097	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30810557	AAAGGGGTATCATCC[A/G]GTTTTTCTGTGAACT	84182
rs537754235	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30886598	AAGGACTGTGGCTTA[C/T]GCTTTTGCTGTCCCA	84182
rs537763026	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859847	TAATCTCCCCTGCCT[G/T]ACCCCTTTTGGCAGG	84182
rs537787928	snp	A/C	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30848402	CCACACAGCAGGGGA[A/C]GGGTGGGCATGAGGT	84182
rs537788013	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853983	GCTCTGGAGCCCCCC[C/T]GCCTGCCAGAGGAGA	84182
rs537797969	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30775806	CTGGGACACAGAACA[A/C]ATATATATTTATCAT	84182
rs537828688	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30879756	CTCCATACCTTGTCA[A/G]TCACCATCAGGGTAT	84182
rs537840181	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30802842	ACCAACCATCCCAAC[C/T]GACCAACCAAACCAA	84182
rs537842171	snp	A/C	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30866928	CCAACTCTCCCCCTG[A/C]CTCCTGGGCTCCCAT	84182
rs537852610	snp	G/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30802418	GTTTGGCTGCTTTCT[G/T]TTGTTCCTTCAGTAT	84182
rs537865940	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30833747	AGTTACTTCCTAGAT[A/G]CAATGGGGGTACAGG	84182
rs537884056	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30831565	CCGGCATGGTGGGTG[A/C]GAGAGGGTGGAGGTT	84182
rs537891918	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30885703	CAGGTAAGGGCAGTG[C/T]CCACCCCCCCCCCAA	84182
rs537914020	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30808558	AGGCACAAAGTAAGC[C/T]CACCCCACTAGGAAC	84182
rs537958202	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30838239	CTCTGGAGGGTGATG[C/T]GTGGGTTGATGGGAA	84182
rs537961195	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30890996	CCTTTTTCTTCCTCC[A/G]TGGCAGTTAGATTTT	84182
rs538005577	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30855417	AGCCTGATGGCATCC[A/G]TGTGTGGGATCTGGC	84182
rs538034383	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30814439	TTCGCTGCATTGTTT[C/T]TTATTTTTATCACGT	84182
rs538083634	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30883687	AAGTGCTCCCCTTGC[C/T]CCGGCAGGCCCTTCA	84182
rs538092928	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30837868	CATTCTGAGCCCTGA[C/G]AGATGAATCCACACA	84182
rs538098990	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30813138	GGTACTTTCAGCCTC[A/G]TGCTTGCATTAGATT	84182
rs538099119	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30890348	CATCCTTACATTCCC[C/T]GATGGTATGCACGAT	84182
rs538116175	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30842501	GCACATATGCACCTA[C/T]CTACCTACCCACCTT	84182
rs538177442	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30867434	TACCGAATGCCAAAT[A/G]CTTTATATAGTTCAT	84182
rs538205772	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30845230	GCTTCACGGTGGAAC[C/T]TCCCCTTTGGCTTTA	84182
rs538219478	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30841212	TTCCCTCCCCACGCT[A/G]TCTCCCCTCTGCCAA	84182
rs538238575	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30805897	GAGCCATGTTTGCAC[C/T]AGCAGCAGAGACAAG	84182
rs538241686	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30876541	GAAAGGGCTGGGCCC[C/G]CAGGTAAAGCTGGAT	84182
rs538243354	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30889046	AAGATAGAGAGGGGC[A/G]GGGTGAAGGGGCCTG	84182
rs538247255	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30798814	TGCATCTTACTTTCT[A/G]TCAGGCCAGTGGTGT	84182
rs538249132	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30805290	GGGAGGTTGGGCAGG[C/T]AGTTAGCAGGAGTAG	84182
rs538269149	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30829366	GCAGCTAGAGACTGC[A/G]GATGTTGAGACCAAG	84182
rs538289102	snp	A/C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30884944	ACTTCCTTCCCCTGC[A/C/T]CCTTGTTCACTTGCA	84182
rs538298412	snp	C/G	0.00358779	0.0422022	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30881968	CTGTATGGCAGAGGC[C/G]CTGCGAGCAGCAGCA	84182
rs538309013	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30887902	AGGGATACCCACGTG[G/T]CTCATCCTAGAGCTG	84182
rs538310423	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30811228	ATGTATTATAGTAAC[G/T]TATACTATAAGACAG	84182
rs538314435	in-del	-/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30823595	CTTCAAAACTGCCCA[-/T]TTCTTTTTTCATAAT	84182
rs538317906	snp	A/G	0.000782256	0.0197615	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850512	CTGGCCCTCGCAGAC[A/G]TTGTGTGGCGGGCAG	84182
rs538381594	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850189	CAGAGCCCTCTTTGC[A/T]CCTGTGGGCCCTTTC	84182
rs538417029	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30770721	GAACCCAGGTGACTA[A/G]GTTCGGGGAAAATGT	84182
rs538419427	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30877647	GGCCCAGCAGCTCAG[A/G]CAAAGCCCTTCCCTC	84182
rs538439086	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30873834	GTGCCTTTCTCAGCA[C/G]CTGCTGCCCCTGACG	84182
rs538440208	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30773723	TTGTTACCAGTACTG[C/T]GCCCTTTCTGTAATC	84182
rs538474325	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30813768	TGTGTATGAGTGGTG[C/T]AATGCTCAAAATTTG	84182
rs538477461	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30806506	AAAAAACAGATGGAT[A/G]TATTCCTGAATAGAT	84182
rs538484011	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30820556	TCTCTGGCAACTACC[A/G]ATCTGTGATATTTCA	84182
rs538504514	snp	C/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30776679	CATGTGGATGATGCT[C/G]AACAAATAGCTGGCC	84182
rs538507657	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30823700	TGAGATTTTTGCTCC[A/G]TCTTGAGTCTTTGGG	84182
rs538540906	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852754	GGAAGACATACATTT[C/T]TGTATTTTGTAAAAT	84182
rs538544072	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30790005	AGGCGAATTAAGAAT[C/G]ACCTCTGCCATCAGG	84182
rs538556268	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30860592	TCTCAGGAGGGCCAG[G/T]CTCAATGATGCCAGT	84182
rs538608582	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882456	TCCACCACCAACCCC[C/T]ATGACAGAGAGCAGT	84182
rs538610819	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30846832	TTCTCATAAGGAGCG[C/T]GCAACCTAGATCCCT	84182
rs538618624	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875768	GAGCTGGCTGAAATT[C/T]GGGTCCAGTTAGAAT	84182
rs538622336	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30868609	CCAGTTCTGTACTCT[C/G]TCTGGGCATTCATCT	84182
rs538632189	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30819640	CTGTCAAATTTTTGA[C/T]AATATGTTTTGAAGC	84182
rs538661791	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30888260	CCATGGTGTTTTTAC[A/G]GAGCGAGTGGTCTCA	84182
rs538737257	snp	A/G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30861301	AGCGGTAAGGATAGC[A/G/T]TCTGTGAAGCTTCCC	84182
rs538752604	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30846999	CACAGACCAGTGCCA[C/G]TCTGTGGCCTGGGGG	84182
rs538760595	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30832361	GTCCTCCAGTAATCT[A/G]GAATCACTCAGGTTA	84182
rs538788083	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852464	GGATGGGCTCCTGCT[A/G]GAGCTGGCTTTACGG	84182
rs538789650	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852067	GGGTGAGTTCAAAGT[A/G]GGGAAAAATGAGAAA	84182
rs538802543	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30817104	TAGAGGAAGCCCCTC[C/T]GGAGGCTCAGAGTCC	84182
rs538816805	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30779759	TGATTCCCAATTCTA[C/T]TGTAGGAGTGATGAT	84182
rs538830366	in-del	-/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852470	GCTCCTGCTAGAGCT[-/G]GCTTTACGGCCAAAA	84182
rs538844401	snp	A/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836221	TGGTTCCATTTTCTT[A/T]CCCAGTCCTGTCCTC	84182
rs538849499	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30863869	ATGCAGGATTTCATG[C/T]TTGCCAAGCTTTGCT	84182
rs538851827	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30857535	TGGAGTGCAGTGGCG[C/G]GATCTCGGCTCACTG	84182
rs538856995	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30794049	CAGACTGGCAAATGG[A/G]ATATGGGCTGGATTT	84182
rs538874610	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30837296	ATTGCTCACCATGCT[C/T]GGCTACCAGGGTGGC	84182
rs538874630	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30831766	TATGGAATCTTCCTA[C/T]GAACATCATTCCCCT	84182
rs538935656	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836832	GATGGCGTGATTTTG[A/G]TGTTTCTGCCCCAAT	84182
rs538986054	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30792807	CAAAGAAAACTTTTG[C/G]CTTTATGTTTGTTTT	84182
rs539007281	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30856086	GCAGGCTCCTGGCCA[G/T]CTGGAGGATGCCCCC	84182
rs539009779	snp	A/C	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30775276	GACCAACTAGCTATA[A/C]ATTGAGGGTTCCCAC	84182
rs539016827	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30812621	TTCTTGTTACATGGG[C/T]ATCCGCAAGCTCTTG	84182
rs539053340	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778158	AAAGCTTCATATACT[A/G]TGGTTCCAAATGTAG	84182
rs539085891	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30862012	TACTTGAGAAGACAC[C/T]CAGCTCTCTCTGATT	84182
rs539107690	snp	G/T	0.00478085	0.0486577	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30781365	GAATATTTGATATAG[G/T]CAAGGATGGAAAATA	84182
rs539145651	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30780699	TAGATAAAAATGCCT[A/G]TGTAAATTGAGATTT	84182
rs539162807	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30834779	TCTTCCACCAGATAC[C/G]CTAAATCATCTCTCT	84182
rs539181723	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30861300	CAGCGGTAAGGATAG[C/T]GTCTGTGAAGCTTCC	84182
rs539225781	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30871514	CACACCTCTGCTCAC[C/T]GGGATACTGAATTGT	84182
rs539233546	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30787157	CTGCAGTCTCTTCTA[A/T]TAGACCAGCTGTCTA	84182
rs539277235	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30834282	TCCCAAACCTCAATT[A/C]TTGACTTCTGTGCAC	84182
rs539322332	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30881522	AGTTGTCTTTACCGT[A/G]CAGTTCTAGTTCAAG	84182
rs539328149	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30802362	ATTTTGCACCTTAGG[C/T]TTCTTGATTATCTCA	84182
rs539338993	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30812583	GGCTAGCCCAAAACA[C/T]GCTGAGGGAGCAGCT	84182
rs539342877	in-del	-/GTGAT	0.00557542	0.0525036	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30889739	CATCCAATGGAGTAA[-/GTGAT]GTGATGATGCTGGCA	84182
rs539346949	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30799460	TGGAGGCCTGTTCCA[G/T]GCTGTTCCTGGCTGC	84182
rs539416599	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30815360	GAGGGAGGCTGGGCT[A/G]CCAGGAAGCCCTAAT	84182
rs539430770	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30788149	CAATATGGTGTTTTG[G/T]TTGAAGTGTATGAAG	84182
rs539433623	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30838691	CTGGCTCTCAAACCC[A/G]GCACACTGTGGAATC	84182
rs539448115	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785023	CTTTGTCTCGTGGGC[C/T]CTCTCTTGTTCTTTC	84182
rs539452452	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30874782	TGTTAAAACCCCACC[A/G]TCACTAATGAAGTTC	84182
rs539465247	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30814899	CACAGCTCTTATATA[A/T]ATGCTTACGCAGGGG	84182
rs539513772	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30874355	CACATGGGACAGAGA[A/G]AACCAGATGTGGGTG	84182
rs539515683	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30881141	CCTGGCCCGTGGCAC[A/G]TACATAGCTGGATAA	84182
rs539532398	snp	A/G	0.00318978	0.0398085	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30783842	ATTCTAAAAGGCAAC[A/G]GAACACTGCAGAGAT	84182
rs539537585	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828557	TCAAGGCACACAGAG[A/G]CAAGGCCAAGACTAG	84182
rs539541723	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30784465	TCCCTGGTCTCCAGG[G/T]CTCTAGTGATCTTCC	84182
rs539552560	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840486	TGGTGATGTCCTTGG[C/T]TTCACAGCTGACTGG	84182
rs539557809	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30820522	AGCAGTTTTTCTCCA[C/T]TCCTCCCCCAACCCC	84182
rs539562640	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30849786	TAAAGATCTGAGTGC[A/G]TCTCAAACTCAGTAA	84182
rs539570513	in-del	-/CAGAGC	0.00016102	0.0089713	utr-variant-5-prime, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771474	CGTGGGCCTCGTGGG[-/CAGAGC]CAGAGCCAGAGCCAG	84182
rs539575214	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30797671	TCCCGCATCTAGGAG[A/G]TATGGGAGCCTTTGG	84182
rs539616920	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30867591	CCTCTGACTTTAGAG[C/T]CCAAGTTCTCTTGGT	84182
rs539618255	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30845868	CATCAGGCCGGCAGC[C/T]GGCCTCTCCTCAGTC	84182
rs539625584	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30880578	GGGACTCTCTCCCTG[C/T]CGTGAATGAATGCTG	84182
rs539632024	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30803747	CTCATTCCTAAAGAC[C/T]GAAGCAGCTCTCTTG	84182
rs539641260	snp	C/T	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30873701	CTGATGCCCCTTCTT[C/T]ACCATCTCAAGAAGG	84182
rs539655953	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30796231	CACATTTCCCCCTGT[C/G]TCACTGTCACATCTG	84182
rs539688419	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30886429	TGCCCTGCAAGAACC[C/T]CCAAGCCACACAGCT	84182
rs539713709	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30878830	CATTTACTCAACCAG[C/G]AGCACGTCCTCTCCA	84182
rs539715058	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30892098	TGGGGCAGGTCTCAT[A/G]TACCCCAACCTGGGT	84182
rs539730216	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850932	CAGGTTGAGTCAGTC[C/G]TGACCCCACTGTACT	84182
rs539833202	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30798059	TGGAAACATCATAGA[A/G]TGTACTTACACTGAC	84182
rs539880357	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30818044	GACTCTAGCAGGGAT[A/G]CTTCCAATGCCTCAG	84182
rs539880463	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30787414	TTAATCTTGTGGGAG[C/G]TTGGCAGAATGTAAG	84182
rs539907250	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30878082	GAGTCCAAGGGGGTC[C/T]AGCACCCAAGCCTGG	84182
rs539912481	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840864	GTAAGTCAGTGCTCT[C/T]TCTGGCAATATCTTA	84182
rs539916820	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30793707	TCATATAATACATGG[G/T]GGGGAGGGGCTGCCC	84182
rs539925855	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30786196	CAGGCCTCCTTTCCT[C/G]CCCTTAGCTTACCCA	84182
rs539957592	snp	A/C	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30831447	AATGCACTTGCTGAG[A/C]AAATAGAAAGATAAG	84182
rs540021071	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30876347	TCCAGTATGACCTCG[A/T]CTTAACTAATTATGC	84182
rs540038059	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30870686	AGACAGAGACTCAGG[A/C]ATGTATTTTAGGCTT	84182
rs540042039	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30799740	ATGTCATGCGTGTCA[A/G]GCTTTGGGAAGCAAT	84182
rs540064668	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30851352	TGTTTACTCATCTGG[A/T]AAATGGGGATGATTA	84182
rs540080334	snp	A/G	0.00478085	0.0486577	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30885854	GTGTTCCATGTCTGC[A/G]AGAACTTTGCTGACA	84182
rs540082881	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875878	GTGTTCTGGGGAAGA[C/T]GGTTTGAAAAGGACT	84182
rs540086982	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30799014	AGCCCAAGTTAGTAG[A/G]GTTGCTCACAGCTAC	84182
rs540088776	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30772443	ACTTTACTCACTGTC[C/T]CAATTTCGTTATCTG	84182
rs540093457	snp	A/C/G/T	5.04236e-05	0.00502094	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882203	GCTTCCTGAAGACCC[A/C/G/T]GAGGTTCCCCATCTG	84182
rs540102379	in-del	-/TTTC	0.0280931	0.11514	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30822162	TACCCACAAAATTTC[-/TTTC]TTTCTTTCTTTCTTT	84182
rs540112558	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30845508	CTAGGATTTCAGACA[C/T]GATCCAGCTTAAAAA	84182
rs540130916	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30832870	TTAACTTTCTTTCCT[C/T]ATTTATCTTTAGCCC	84182
rs540175147	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850610	CTGCTGGCAGCTGCC[A/G]GCAAGCTGGCTGTGT	84182
rs540200132	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30838374	GGATGGTTCAAGCAG[A/G]GTTCACGGGGGACCA	84182
rs540231695	snp	A/C/G	0.000165667	0.00909979	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859312	CTGCCATCCTGTCCA[A/C/G]GTCTACAGAGCTGTG	84182
rs540257664	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30783675	TGTTTTCAAAATCTC[C/T]GCTGTGAAGTGCTGT	84182
rs540269566	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30801235	TGAAAACATCTGCAC[C/T]TCATGGGATGAGTAA	84182
rs540280106	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30810681	CTTACCTTATGGTCC[A/G]ACATTAAAAATGGAA	84182
rs540290211	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30813364	CAGGTCCTGAATTCT[A/G]TGTGAGGCGGGCCTT	84182
rs540293564	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30871200	GGCTCCCTGGTCTCA[C/T]GTTGCCCCCCAGAGC	84182
rs540316043	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30831976	TGTCTTCCTGGCCAA[C/T]ATGTCGTTCTGGAGT	84182
rs540333442	snp	A/C	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30807770	TTCTGTTCTAATTAC[A/C]GGTGCATGCAGCCCG	84182
rs540335798	snp	A/G	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836972	CGTTCCCTCTCCAAG[A/G]CAAAAGGTGAGGGAG	84182
rs540356423	snp	C/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30843092	CGTGAGAACAGGGAC[C/G]TTCCTGAGCTGGTTC	84182
rs540377625	snp	A/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30821819	CTTAGTAGTTAATGA[A/T]GTCTTCACTAATCTA	84182
rs540438413	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30874677	CAACAGCAGAAGCAG[A/G]GCTAGAACTCATACT	84182
rs540464892	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30812730	TAGGTCTGCTGAGCC[C/G]TGGGAAGCTGATTCC	84182
rs540475075	snp	C/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30812275	TATGTGTGTTGAGGG[C/G]GGGGGGGTATGTATG	84182
rs540476919	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30819210	TCTCCATATTACTTT[A/T]ACTGCTTCCCGTAAG	84182
rs540505143	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30792162	ATCCTTACTTTTATT[C/T]TTTACAATAAGCCTT	84182
rs540587919	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30826255	GCCGTTATTCAGCCT[A/G]TGACACCACGTGACA	84182
rs540590612	snp	G/T			missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840819	ACAGAAACTCCTGTT[G/T]GAAGGAGATAGCAAA	84182
rs540594452	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30794849	CTCTAACCCTCGTCT[C/T]TCTCTCCCTCTCGCT	84182
rs540607449	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30835355	CACTATCATGAGAAC[A/G]GCACAGGAAAGACCC	84182
rs540654619	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30874562	GAATGTTGCTCCACA[C/T]GTCACTTTCTCCAAG	84182
rs540685193	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30800846	CTCCTCTGACACTGG[A/G]GATGCCTGGCAGTTT	84182
rs540691623	in-del	-/A	0.00557542	0.0525036	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791897	CTAAAAAAAAATTGC[-/A]AAAAAAACTCAATGT	84182
rs540704826	snp	C/T	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840300	TGGGGCAGAAGAGAG[C/T]GCAGAGCTCATGTAA	84182
rs540708866	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30845943	GAGAAGAGGCTGTGC[C/T]GGCTTGGCTCACAGA	84182
rs540769766	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30842542	ACTGAAAAAAATGTG[A/C]AGAGTGTGCTTAGCA	84182
rs540781926	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30848636	GTTTTCATAGTGAAC[C/T]GTGACCTGGGCCAGT	84182
rs540790995	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30809537	ATCGATGGTTCCTCC[C/T]AGGTAATTGAAGGAA	84182
rs540796387	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30807138	ACCAAGTATTTTGCC[A/G]CCATCTGAGGATTAG	84182
rs540822372	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30769691	TGGTGCAATCTGCCA[C/T]ATTAAAGCTACGTCC	84182
rs540827359	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850732	GACTCAGGGAGAGCC[A/C]TGGCCTTCCATGCGG	84182
rs540850187	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30841050	GTTTGTTTCTGAAAG[C/T]GGGGAGGGTTCTCAG	84182
rs540867736	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30889270	AAATCTCAAATGCTC[A/T]TCGTGTTGCTGCAGA	84182
rs540911507	snp	G/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30891780	GTGTATTTGTGTTTC[G/T]TAAGAGACTGGTGTG	84182
rs540923869	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30822128	CCTAAGGGCAAGAAC[A/G]TTTTCCTCCACAACC	84182
rs540963262	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859663	GGATGGACAATTGAG[G/T]CTGAGACCCAGGAGA	84182
rs541014373	snp	G/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30797818	AGTTAGGCAACTGCA[G/T]TAGTAGAAGAGAGCT	84182
rs541042355	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30805040	TCTCTAGGCAATAGA[A/G]AGGGATAGAAAGTTC	84182
rs541052757	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30773891	CCCACCTACCTCTCA[C/T]CCACCCATCCTTATA	84182
rs541057141	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30887585	GAAGCGTGAGCCAGC[C/G]AGGACCATGGTTTCC	84182
rs541070394	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30804147	TGATGCTGAGTTATG[C/T]TAGGGGCATATTGGG	84182
rs541071840	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30880699	TTTAGGCACGTCCAG[C/T]CACGTCCTGTAAGAC	84182
rs541080557	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30810108	TTGAACCTGGGAGGC[A/G]GAGGTTGTGGCGAGC	84182
rs541125645	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30892327	CAGGCCTCCAATGTG[G/T]TTGGCCCTGGGGACT	84182
rs541168638	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30807300	GCAGGTATCTAGGAA[G/T]CAACCCCTGGATCTG	84182
rs541208515	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30886331	TCTCAGAGAGTTTGC[C/T]ATCAGCCAAAAGTCA	84182
rs541220884	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30772011	TTCTTGACGGTCAAA[C/G]CCTTAGTCATTTTAG	84182
rs541237765	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30862953	TGCAGCGGAATGACT[A/T]TGATTAGAGCGGCAG	84182
rs541257686	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778252	AAACTTCAGCCTTCA[C/T]TTAGCCCATGGGGCT	84182
rs541258040	snp	C/G	0.000847607	0.020569	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771561	TCAGCAGAAAGGTAA[C/G]GGCTCGCCCCCTCCA	84182
rs541284367	in-del	-/A			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30792845	TTGACCTCTGCTCTT[-/A]ATTTTTATTATTTTC	84182
rs541303329	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785208	ACCCTCTTACACTCC[A/G]CTCAACTCCCCTCAC	84182
rs541319211	snp	A/G	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30835860	GGCAGCAGGTGTAAT[A/G]ACAAGGGGGCCTTAG	84182
rs541348462	snp	A/C	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30855659	GTCTATGAGATGGAG[A/C]CTCCCCCTCAGCCTG	84182
rs541350774	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30777693	AAGGAACACCCCTAA[C/T]ACCAGGCTGAGCTGT	84182
rs541364549	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30835384	CCACTCCCATGATTC[A/G]GTTATCTCTCACTGG	84182
rs541376539	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852582	CCTGTGTCCTTCTTC[C/T]TCTTTCTTTAGCATC	84182
rs541414491	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30770204	GAATGGTTTGAATCC[A/G]GGAGGTGGTTGTTCA	84182
rs541416483	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30776830	TTATTCCTTCTGTCT[C/T]TCCTGCATCTAGAAC	84182
rs541419765	snp	C/T	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30854861	ACCGGAGGGGCAATC[C/T]ACCTGAAGTGCTTTC	84182
rs541445291	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30860628	CGCCCCCATCCATGC[A/G]GGGGCCCTCTGGCTC	84182
rs541455289	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30884010	TGGTGTTTGTGCTCA[C/T]GATGATGACCTCAGC	84182
rs541455397	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30776172	CCAAGTGATCTTTCA[A/G]AAATATGTCAGTTCA	84182
rs541467632	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30890043	ATTGATTGCCAAAAG[G/T]CCATACAACCTGATT	84182
rs541469419	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30773308	TCCTGAAAGATAGGT[A/G]TAAGTATTCCCTTTC	84182
rs541527640	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30779533	TGATATCTCATGTGG[A/C]AGTCCAATATGCAAA	84182
rs541556430	snp	C/T	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30860339	CTCTGTGGCCTCGTG[C/T]GCCAGGCTGCCTGCT	84182
rs541571321	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30887241	GAGCATTCTCTGGGC[A/G]CTGTCACTCCCCACT	84182
rs541579105	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782439	AGGTGCAGTGGCTCA[C/T]GCCTGTAATCCCAGC	84182
rs541618408	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882663	AGGCAGTGGCGAGCC[A/G]TGGAAGGTTTTGGAA	84182
rs541621482	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30869723	CTCTATTTCCAAATA[C/T]ACATTCTCAGGTGCT	84182
rs541621730	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30843395	TGCTGCCAGCTGCTT[A/G]GATCAAGCCTTGGCC	84182
rs541623222	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30866251	ACCCAGGGACCTTAC[A/G]TGTTCATGCAGGGCC	84182
rs541638611	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30889512	TCACTGCCGAGGAGA[A/G]GTCTGACTTCACCAA	84182
rs541679089	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30874996	TTTAAAAAATAACAT[C/T]GTTTAAGACTCACCC	84182
rs541684683	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791761	TCAGCCAGAGCTCAC[A/G]CACCTGGAAAGCTGA	84182
rs541721487	snp	C/T	0.000149255	0.00863743	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791418	GGGACAGGGCCAGGC[C/T]GAGGGATCCCTCCGA	84182
rs541767907	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30849237	TCCTCCCCAGCACAG[A/T]TCCGCATGGAGCTCA	84182
rs541809766	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30783937	TTGAACCTCTATTAT[A/C]TGGAAAACAATGACA	84182
rs541878807	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30820603	TAATATATAAACTTA[C/T]GGTGTCAGGCTTCTT	84182
rs541887352	snp	A/C/G	0.00016562	0.00909867	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828722	GTGGATGGTGAGCTG[A/C/G]GTGCCCTGCGGCTCG	84182
rs541893821	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30796437	AAGTGAGTATCTTCC[C/T]AGAATACAGCCTTGA	84182
rs541897733	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30790263	AAAGGAAGTACAGTG[C/T]ATGAGCCACATACCA	84182
rs541899856	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30792300	ACTTATTAATATTTC[A/G]TGTAGGGGTTTTGTG	84182
rs541928288	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30873381	CTGGGTCCCAAGCCC[C/T]GTTCTCTGTTTCACT	84182
rs541950696	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30834443	TGCTGTACACAGCAC[A/C]GGGACCCTGGGCCCA	84182
rs541954459	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30827129	GAGAGCAGAGGTGGG[G/T]GTTCAAGAGAGATGT	84182
rs541984980	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30871449	CCTAGCAGGACAGCA[A/G]GCCGGGAAGGAGGAT	84182
rs542004352	snp	C/G	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30795842	TGACGTTGGCTGAAT[C/G]CTGCTCAGGCTGCCT	84182
rs542040810	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30879211	GAAATGATTAAGGTA[A/C]AATGAGGTCACTAGG	84182
rs542049831	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30788292	GTTTCTTAATGTGAA[A/G]TCTTAAACCATATCA	84182
rs542065562	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30885103	CTTGAGCAGTCATGC[A/G]TGGAAAATAATTCTA	84182
rs542075984	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30884456	TTCAAAATGATGAGA[A/G]AAAGGCAGCAGTGGG	84182
rs542090201	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30841377	AACATCTCTGTGCAG[A/G]CACAAATGATACAGG	84182
rs542109654	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30815930	GAAGGCAGTGCCTCA[A/G]ATATCCAGCATGGGA	84182
rs542119039	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30770752	ACTGGGCTTGGTTAG[A/T]AACCCAACTTTCCCA	84182
rs542123987	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30794316	CAAGGGGAGACACAC[A/G]TGTGCACATATAATT	84182
rs542150260	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30837844	CACACTGTGCCTAGC[A/G]GGAGCTGTCATTCTG	84182
rs542244089	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30868205	GGGGTAGGGCTTTGG[A/G]ACTCTAGGGCTTGCT	84182
rs542262841	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30823095	CATAAGTGATGTTGT[A/G]TATTTCCTGTTACAT	84182
rs542285406	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30798880	AGGGTCCATGTGCTT[A/G]CAGTCCACACATGTG	84182
rs542287823	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30789598	CTCGGGAATGGTGAC[C/T]AATGTCTTCCTCACT	84182
rs542348378	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839409	GTTAATCCTGTGAGC[A/G]TTAGCTGAGCTATTC	84182
rs542362647	in-del	-/G	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30818757	AAATTAATGATTTAA[-/G]GAAAATGATTATAGG	84182
rs542364124	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828046	AGGGAGCTTTAGAAA[A/C]TGCTCCCTCAAAGGG	84182
rs542392129	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872998	TGGGGGGCCACAATG[C/T]GTAGCATGGACGGGC	84182
rs542395582	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30805364	AGTTGTTTCTGGATA[C/T]GTCCAGTGGAGCTTT	84182
rs542397647	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30798575	GATCTTGGCTCACTG[C/G]AAGCTCCGCCTCCCG	84182
rs542411498	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30844645	AGGCCCTGAAGGTCA[A/G]AGGCTACAGAAGGTT	84182
rs542420921	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30860048	GGAAAGTACAGTCAA[C/T]TGCCCCATTCACTTT	84182
rs542455647	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30878512	GACTTCCAGCTGGCT[C/T]CCTCAGTCCCACACC	84182
rs542460984	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30805004	GCAGGCCCGACAGGT[A/G]CCCCAAGAGCCAGAC	84182
rs542473651	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30887494	GGCATGCGTTGGGGA[C/G]GAGGAGGAATCAGGT	84182
rs542499033	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30775957	TCCTTTCTTGTGCAC[C/G]TCATATCCAGTCCAT	84182
rs542504962	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30881528	CTTTACCGTGCAGTT[C/G]TAGTTCAAGTCCTGC	84182
rs542510590	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30816546	TGTGTTCTCTGCAGC[C/T]GAACAGCCTGGGCCC	84182
rs542523954	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30843929	GACCTTATGGGGGGG[C/T]CTGCCTGGCTGGACC	84182
rs542531387	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30807820	TGCTCAGTTGATCAC[A/G]ACCCTCTCACGCGGA	84182
rs542548891	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30890575	TTCAAAATATGCAAG[A/G]GGAAAATTTAGTCTT	84182
rs542569361	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30842507	ATGCACCTACCTACC[G/T]ACCCACCTTCCTTCC	84182
rs542577247	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30810216	ATGTTTATAATAAGT[C/T]AGAAAGTTGAGGCAT	84182
rs542638538	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30848040	CACCTGGCCACTGTT[A/G]GCTTTTAAAATCTTA	84182
rs542641039	snp	C/T	0.00318978	0.0398085	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30864095	TTTTCATGCAGTAGA[C/T]TCTTGGCCTTCATTA	84182
rs542643102	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30871181	GGGACAGACCTGGGA[C/T]CCAGGCTCCCTGGTC	84182
rs542665307	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30867359	TCTTGGTTATTGTTT[C/T]TTGTTTTGTTTTGTT	84182
rs542666590	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30795428	GTGCCCTGTCACATG[G/T]CTTCAACCATGGAGC	84182
rs542692904	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30842120	TTAAAATTTTTTCCA[A/G]TGGTTTTGCACAATA	84182
rs542706059	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30887076	AGAAATTGAAAATGT[A/T]ATTCCAGCTGGGTAT	84182
rs542712298	snp	A/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30812638	TCCGCAAGCTCTTGC[A/T]CTCCAAGGAATCAGT	84182
rs542798384	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30847011	CCAGTCTGTGGCCTG[C/G]GGGTTGGGAACTCCT	84182
rs542850147	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30818334	TTATATTTTTGTATT[C/T]TATGTTTACAGGTAT	84182
rs542921659	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30824944	CCTGGTCCCATGGAG[C/T]CCAGAACACCAGCAG	84182
rs542928138	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30816594	GATGCGGGGCCATCC[A/G]TTTCTCCCTCCCTCC	84182
rs542968510	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30845645	CCCAGAGGCAGCCCC[C/T]GCACTTTCCTGCCTG	84182
rs542969454	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30787282	GGCCACATCTTGATG[C/T]CATACCCCATTCTAG	84182
rs542973640	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30781243	ATATTGCTGCATGCA[C/T]AGCTGTGTTTATCCA	84182
rs542985907	snp	C/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30858577	CAGAAATTAGCAAAA[C/G]CTATCTTTTTTAAAA	84182
rs543005463	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30860019	TAGCAGATTAATAGC[A/G]CATGAACGGTTGTGG	84182
rs543005748	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30864847	GCTCCTCTCAGTAAT[A/G]GAGAAAAGAGATCAC	84182
rs543019956	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30841192	CGACTGCGTCCGGGC[C/G]TCCCTTCCCTCCCCA	84182
rs543027430	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30800626	AGGGACGCTATTGAG[C/G]GGGCAGGAGGGCCCT	84182
rs543030192	snp	A/G	0.0023933	0.0345097	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850698	CCTGCAAGCCAGCCT[A/G]ATGTGCTGAGCAGCC	84182
rs543069160	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30806251	ATTTAGTAACTTGGC[A/G]TGGTGAGGTTGAAAG	84182
rs543079210	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30842774	AGAACCCCTGATTCC[C/T]CTTCATATGCATCCT	84182
rs543090929	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30883319	AGTACCGTTAGGCCC[A/G]AAGGAGGCAGGACAG	84182
rs543100344	snp	G/T	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30885965	GAGTGGGTGAGTGGT[G/T]AGTGGGAACACTGCC	84182
rs543102996	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882845	AAGGGGGCGGGTCTC[A/G]GGAGTGGTCAGCGCT	84182
rs543109187	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30889116	CCTCCCTTCTGCCAC[C/T]CTCTGGGAGTCTGGA	84182
rs543144983	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30889823	AAGTGTTATCATATA[C/G]CTCTTGTCACAGGTT	84182
rs543147374	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30888617	ACTTGTCCTTGTAAT[C/T]GACTCACAAGCTTTC	84182
rs543164738	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853206	ACTCCAGCGGTACCG[G/T]CCAGCCTTTCACTCA	84182
rs543173911	snp	A/G	0.00318978	0.0398085	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30814881	TGTTTCGAACATGTG[A/G]CTCACAGCTCTTATA	84182
rs543225907	snp	A/C/G	9.97032e-05	0.00705994	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859229	AGGTGCAAATGGGAT[A/C/G]GAGCTCATTTTTCTC	84182
rs543231346	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30822908	CTTGGCCTCCCAAAG[A/G]GCTGAGATTACAGGT	84182
rs543234878	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30774949	CCCAAATGTCTATCT[C/T]TAGCTGAGACCTCTC	84182
rs543273530	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30774460	GCACATGTTGTGCTC[C/T]TGCAGAATCCCATCT	84182
rs543273577	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30780787	GAAAAAGCATAAGGG[A/T]TAGTCAGGCAATTCA	84182
rs543288430	snp	C/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30821730	TTTTCCTCCATTTCT[C/G]TTATTTATTTGCTCC	84182
rs543302271	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30804928	GCTGTGAGCAAAGAG[A/G]TGGGCAAGTTGGTGT	84182
rs543309683	snp	A/G	1.65633e-05	0.00287774	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828663	CTCTGGTACATTGAT[A/G]TTTTCTATTTTCCAG	84182
rs543324000	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30827789	CATACATCTTCAGGA[A/G]GAAACCAATTCAATG	84182
rs543355316	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30830358	TAAGTGCTTTAATAA[G/T]CCAGGTTCTGTGATG	84182
rs543356038	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30803339	TTGAGATGGATTCTT[A/G]ACTTTGCTTGGAATT	84182
rs543377448	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30864624	TGCTGGGTGCTGGGT[A/G]CCATTCCTGGTGTGA	84182
rs543398382	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30806618	TTAGTTGTGAGAGCC[A/G]TGGCCAGGGCTCCTG	84182
rs543409426	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30779430	GGCTGTCCAGCAAAT[A/G]TTGCTGTGTGGTTGG	84182
rs543415873	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30863362	GTGGTGGTGTGATAG[A/T]GTGTGTGCGGATGGG	84182
rs543444430	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778822	CAGTGCTCAGCCTCC[C/T]GCAGTTATTCCCTGT	84182
rs543448172	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30773042	TCCCTCGCATGTTTT[A/T]TCTGGGCACACTAAG	84182
rs543455471	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30879438	TGAGCCATCCAGTCC[A/G]TGGTATTTGTTATGG	84182
rs543457967	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30857045	ATCACAGAATGAAGA[C/T]GAGGTTGATTTAACA	84182
rs543463961	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30815382	AGCCCTAATCAGAGG[C/T]AGCCTTAGTGGCCCA	84182
rs543474154	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771896	CAGCGGGCAGGCCTG[A/C]GCCCTAGCCTGGCTG	84182
rs543484176	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30815961	TAGATTAAAATAAAC[C/T]AAGATGAGAGTCAGG	84182
rs543529687	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785125	ATGGTGTGCCCAACA[C/T]AGTCTCAGAGACAAA	84182
rs543544105	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30891359	CTGTTATTCAGTTGT[C/T]TCTAACCCTGGACCA	84182
rs543564986	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30784554	TGCCGCTATCCTGCC[A/G]AAGGGCTTCAGACGT	84182
rs543580059	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30864470	AGGGGCTGGATCCAG[C/G]AACCCAGACATTGTC	84182
rs543587451	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30869198	CAGCTGCTCATTAGA[A/C]TGGATGGTTAAGTCA	84182
rs543606398	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30855090	CTGATGCGGTGCATC[C/T]ACCGCCTGGCCTGGG	84182
rs543619420	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30868561	GAAGCAGAGAGCCCT[A/G]AGTCTGGGCTGACAT	84182
rs543637284	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30777629	ACACAAAGGCTCTGG[A/G]AGAGGCTGAAGCCTG	84182
rs543676274	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30777035	TTTTTTTAGAGATAG[A/G]GTCTCACTCTTTCAT	84182
rs543676314	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30783860	ACACTGCAGAGATGG[A/G]AAAAATCTGGAAAAT	84182
rs543694846	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30773724	TGTTACCAGTACTGC[A/G]CCCTTTCTGTAATCT	84182
rs543699486	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30820747	TTACTCATTTGTTGA[C/T]TGACATTTGGGTTGT	84182
rs543752030	snp	C/G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30887674	TGGCCTGGTGGGGGT[C/G/T]GTGTTCATGCAGCAG	84182
rs543758656	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30783321	CTCATGTCTCCTTCT[A/G]AGAAGGACCCCTGTG	84182
rs543761742	snp	A/C	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30880306	CCCTCCCCCGCACCC[A/C]CCCCCACCCCCGACT	84182
rs543790847	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30857621	GGGACTACAGGCGCC[C/T]GCTACCACGCCCGGC	84182
rs543808047	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840247	AGGGTGAGAAAGGAC[A/G]AAGATACACCTAATG	84182
rs543813995	in-del	-/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30867885	TAGAGTCATGGACCA[-/G]GCACACTTGTGCACA	84182
rs543831215	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30851530	ACATACTAAGCACCA[C/T]GTTTTAGATATCGTT	84182
rs543838109	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30781723	TCACATTTTATTCTA[G/T]TTGTTTATTGAATCA	84182
rs543873623	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30823814	GCATATTTTAGTAGG[A/G]CTTAAAAAAACAAAT	84182
rs543934316	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30823200	TATGTCACTCTGTCT[A/G]TCATTGTAAAGATAA	84182
rs543944872	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30830027	GCCATGGAACCCAGT[C/T]ACGGAGAGAGTTCAT	84182
rs543952839	in-del	-/A	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30863655	GGACATCATGGACAG[-/A]ATGTAAACCTAGCCG	84182
rs543979022	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30871679	CAGGCCTCAGAGCTG[C/G]GCACCCTTGAGCAAG	84182
rs543982560	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30825819	TTAGTTTACCATTGC[C/T]GCCATAACAAATTAC	84182
rs543987974	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30867169	AGGGGCCTGACACCC[A/G]TTGGTTCTGACTCAT	84182
rs544001270	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30797726	TCTCACTTGTGTTTT[A/T]ATAGGGTCCCTCTGG	84182
rs544002673	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30829328	TACTCTCCAAAGACA[A/T]GCATTTGCAGGGTTT	84182
rs544045630	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30880693	GTGGGGTTTAGGCAC[A/G]TCCAGCCACGTCCTG	84182
rs544051085	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30837800	GTGGCCTCTGGAAAG[C/T]AGAGTCCAGGTTCCC	84182
rs544052967	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30864838	GGCCCCCAGGCTCCT[C/T]TCAGTAATGGAGAAA	84182
rs544055272	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30876512	CATCCTGTGTCACTG[C/T]AGCCAGGGGCTCAGA	84182
rs544056259	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30849980	AAGTGAGGCTGCTGT[C/G]CCCTTGGCCCTGGCA	84182
rs544062947	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30821952	AATTCAGCAATTGGT[A/G]TGATTTTGTCACATT	84182
rs544089168	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30871103	AGGTTCAGTTGTGAC[G/T]CCCAGGGTCGTGTGT	84182
rs544097021	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30827788	TCATACATCTTCAGG[A/C]GGAAACCAATTCAAT	84182
rs544100351	in-del	-/CT	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30815030	TTTGTGGGACTCAGC[-/CT]CTCGTTGGTGCAGCT	84182
rs544172680	snp	C/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30833912	CACATCTAGGTCATG[C/G]TGATGCAAGAGGTGG	84182
rs544201252	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30832610	TGTTTCCTGGGTTCA[A/G]GTGATTCTCAGGCCT	84182
rs544201595	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859741	CCAAGGCAGCCCTGC[A/G]GTCGCGTGGACAAGG	84182
rs544245300	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30781119	GGTGCCTGGCTAGTC[C/T]GCAAAATCACAGAGT	84182
rs544259220	snp	A/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30865524	CCGTCCCTGGGAGCC[A/T]CCTGCTCCTTTGTCC	84182
rs544285481	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30795706	TCACTGGTCTGCAAT[A/C]CAGGTGTCAGCAGGC	84182
rs544335382	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30832666	AGGCCCGTGCCACCA[C/T]ACCTGGCTAATTTTT	84182
rs544346875	snp	G/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30807715	ATTACAGACATTGTA[G/T]AGAAAAGCACTATGA	84182
rs544371148	snp	C/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30846200	CCAGCCTTTCTACCC[C/G]CTATTGCAGCTTTTG	84182
rs544379205	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30801367	TCCTTTCCAGCATGC[C/T]GGTCATCCTGTGTGG	84182
rs544392895	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30832113	CCAAAGGAGTTTGCC[G/T]TTTCCAAGGGGCTTA	84182
rs544393719	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30884381	TGCTGGTGCTTCTTT[C/T]GTCGGGAGGATTAAG	84182
rs544418527	snp	A/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30843859	GAGGGAAGAAGGAGC[A/T]GCTGGCCTGTTGGGG	84182
rs544459926	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30784177	AGCTCTTCCTCCGAG[A/G]CACTTACTACCTGGC	84182
rs544462237	snp	C/G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30799977	GAGCTTTTTGTGCCC[C/G/T]TCTTAGTCATTGGCT	84182
rs544491669	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30889890	GTATTTATTCTTGAA[A/G]TATCTTTTAAAAATG	84182
rs544504157	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30889378	CCAGCCTGCTTACCT[C/T]CAGAACCTGCTCAGT	84182
rs544509402	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882762	GACCAGTGAGTTGTG[C/T]AGGTGAGAATGGATG	84182
rs544521676	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872575	AGAGGATGCAAAAGA[A/G]GCTGAACTCAGACCA	84182
rs544533178	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30813329	AGGGAAACTTGCCCT[G/T]TGTTAAAGTGTTCAA	84182
rs544547640	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30770141	AATATTAGCTGGGCA[C/T]GGTGGTGGGCGCCTG	84182
rs544590533	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30776152	GTTTATTTTCAACCT[A/G]GCAGCCAAGTGATCT	84182
rs544593465	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30873254	GGCCTCACTCTCACT[C/G]CAGGCATCTGCCTGC	84182
rs544665801	snp	G/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30776536	TGTTGTCTCTCCCCC[G/T]ATAGAGTGCAAGCTC	84182
rs544669212	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872479	TTTCACTGTCATGTC[A/G]TGGAGACCCAGAAAG	84182
rs544674882	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30795034	TTCCAAGCCTCTTGG[C/G]TCCTCAGGGGCACTT	84182
rs544690305	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30835456	GAAATTTGGGTGGGG[A/G]CACAGAGCCAAACCA	84182
rs544695109	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30795579	CCTGACAGTATAGGC[A/G]AATAGAGGGGTGCAT	84182
rs544744350	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30843354	GTAGTGGCAGGTCAG[C/T]GCCAGGCTGCCAGAG	84182
rs544770210	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30849818	TCTGAAGTGTGACTC[C/T]TTATCTTCTATCTCC	84182
rs544815461	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30883917	TGCACCCCACTTTGT[C/T]ATCTGTAAAATGGGG	84182
rs544826405	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840695	TTCTGGGGTGGGTTT[A/G]GGTGAAACCAAAAAC	84182
rs544859828	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30809687	AAAGTTAACAGTGTA[A/T]CATGTATTATAGTAA	84182
rs544901788	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30769744	ATAGTTGCTTCCCAA[C/G]TGTGGTACATGTGCC	84182
rs544920520	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30815573	AAGGGAGATCATGGG[A/C]TAGCAACATTTTGCT	84182
rs544931217	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30824710	TCCTGAGTAGCTGGG[A/T]TTACAGGTGCGTGAC	84182
rs544951443	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853908	TGGGTTGGAGGGCTT[A/C]GCAGTGTGATACACA	84182
rs544953284	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30847870	TCAGCCTCCTGAGTA[A/T]CTGGGACTGCACATG	84182
rs544977734	in-del	-/CT	0.00398564	0.0444627	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30802152	GATGCTTTTGTGCTG[-/CT]CTGTTAGCTATGTTC	84182
rs544980110	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30798006	AGGACCTGGGAGAGT[C/T]TGGGGTGCACCTGTC	84182
rs544996300	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30870487	GGTGGGTGAGCCTCA[A/G]CCACCCTTCCCAGAA	84182
rs545014547	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853189	CCACCTGAACCCTGA[C/T]GACTCCAGCGGTACC	84182
rs545042309	snp	C/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30881362	CACCATGTGAAATTC[C/G]CCTGCTTGGAATGCT	84182
rs545052513	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30804946	GGCAAGTTGGTGTAG[C/T]TGGAGCCCAGGGGAT	84182
rs545055311	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30799031	TTGCTCACAGCTACT[A/G]TCTAAGGACAGTAAA	84182
rs545062941	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30841015	GCCTGCGCAGACCAG[C/T]GTTAAGGGGACTTGT	84182
rs545064372	snp	A/G	0.00398564	0.0444627	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875123	GCCACATCCTGCATT[A/G]AGTCAATGTGCAGAC	84182
rs545068622	snp	C/T	1.65638e-05	0.00287778	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828727	TGGTGAGCTGGGTGC[C/T]CTGCGGCTCGGTAGG	84182
rs545074087	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30874601	TTGGCATGCTTGTTG[A/G]CTTGCCAGGTGTGTA	84182
rs545098281	snp	A/G	4.99879e-05	0.00499915	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882288	CCTGCGTGACTGGAG[A/G]ACTGAGAGGCTCTTT	84182
rs545129342	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30860283	GCGCCCTCCCTGTTT[C/T]CAGGGGCCTCTGCTG	84182
rs545137938	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30846618	GATTCAGACGCAGGA[C/T]CTTTCCCTGTCATCA	84182
rs545143361	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30830030	ATGGAACCCAGTCAC[A/G]GAGAGAGTTCATGAA	84182
rs545145271	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30774853	CTTAGTTTATGGCTC[C/T]CTTCTCTTCTTCTTT	84182
rs545157945	snp	A/C	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30888083	ACAGGCTCTATCAGG[A/C]ACCTTTTTCCCCATG	84182
rs545260532	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30772866	AGAGAGGGCTTCCTC[C/G]TGTTCTTTCTTGAGT	84182
rs545272026	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30773983	GACAGTAAAATTCCA[C/T]TCGTCCTGCTCTACA	84182
rs545297779	snp	C/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30830582	AAAGGGGGAAAAGTC[C/G]CTTATAAAACCATCA	84182
rs545300986	snp	A/G	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30816877	GAGGAAAGAAAAGAC[A/G]GAGAGAAAAAAATAT	84182
rs545309072	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30779580	GCCCTATTTGAAGTG[A/G]GGAAAAGGAGGTCTT	84182
rs545310955	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30891824	ATTTGGAGGGGTGAG[A/T]TGAGCAGGATGGAAA	84182
rs545340105	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30863503	TGTGTGATGGAGAGG[A/G]CATAGTCGTTCCTCC	84182
rs545347673	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850770	ATGCCCTCTCTGGGC[C/T]CCAGTTCTCATGTTG	84182
rs545366880	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30824077	AGTCTGTTTTCTGTA[A/G]CATATAACAGAAAAC	84182
rs545417910	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30855559	AGCCTGAGGGTGATT[G/T]CTCAAATGACCACAG	84182
rs545433115	snp	A/C	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30888437	ACCGAGGATGAGAGA[A/C]CCGGCTATAAACTGG	84182
rs545462186	snp	A/C	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30812026	TACTGATTTATTATT[A/C]TTCTTTTTAAAGAAA	84182
rs545495484	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30774422	ACCATGCATTTCCCT[C/T]CTCTACTAGGTTACT	84182
rs545499854	snp	G/T	0.00398564	0.0444627	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30817359	TCCATGGAGAACTTG[G/T]GTTTGTCTTTTTTTT	84182
rs545529330	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30855077	AGTAGGCCAACTGCT[A/G]ATGCGGTGCATCCAC	84182
rs545583357	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30780048	CTTGCTCCCCTTTGA[A/G]GAGAAGTAGGCAATG	84182
rs545585223	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30864054	GGTCATTGAGGCCCT[G/T]AGAAGGTCCAGTGGG	84182
rs545596606	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30860374	GCTGCTTCTGACCTT[A/G]TTAAATGCGTGTGAG	84182
rs545610099	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30824840	GCTGGGACTATAGGC[A/T]TGAGCCACCACACCT	84182
rs545630623	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30807443	TATCTTTAAAATTCA[A/G]CACACTCCTAGGAGT	84182
rs545631098	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30783229	GCCTTGACTCTTGGC[A/C]CCTTCTTCCATTTTA	84182
rs545652319	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30786059	CTGGGCTTAAGGCAC[A/G]CCTGGGTTTATTTGG	84182
rs545694713	snp	A/G	0.00795532	0.062565	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30833368	GAGAGAGCCTGTGTA[A/G]GCAAGCTTCTGTTTT	84182
rs545710446	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30827687	GTTCTGTGTTCTAGC[A/G]CCAGTGAAAGAAACC	84182
rs545738393	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785689	AATGTGGAATTTGCT[A/G]TCTTTGTTACTGATT	84182
rs545740297	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785358	AATGCCAAGTTTGCT[A/G]TGGGTCTTCTCCACG	84182
rs545746776	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30844045	GTAGGAGAGTGACCT[C/T]GCTTTTGTTTGGAGC	84182
rs545791427	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30808966	GAGAGAGGCAGAGAG[A/G]GAGAAAGAGACAAAT	84182
rs545808214	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850016	TAGCACCTGCCTGTA[C/T]GTGCTACTGACTCCA	84182
rs545830259	snp	C/G	0.0023933	0.0345097	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30784522	AGCGTGAGCTTTCCA[C/G]GAAAAGAGTCTGGCC	84182
rs545834113	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30788913	CATGGACATTCCTCG[C/G]TGAAGTCAGCACTTT	84182
rs545904670	snp	G/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30822381	TTGCCATGTTGCCCA[G/T]GCTGGCCTCAAACTC	84182
rs545923438	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30815724	TCACATCTACCCACC[C/G]TTTCACTGCCTGTTG	84182
rs545943774	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30868473	GATTCGAAGCCCATG[C/T]ATTGTGCAGCCTGCT	84182
rs545950577	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30790398	GCCTCACAGCAGTTA[A/C]GAATTTACCACAGGA	84182
rs545975481	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30776384	TCTGTGTGGCCTGCT[C/T]TTTTGATTCCCTCAT	84182
rs546004115	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30820148	CCTCGTGATCCGCCC[A/G]CCTCGGCCTCCCAAA	84182
rs546025977	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30855323	AATGCAGTACTAGGC[A/T]GTCTGAAGGAGCAGA	84182
rs546031024	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30873430	AGTCTTTTTCCCCTC[C/T]TGTGTGTCAGTTTCC	84182
rs546044834	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30866300	GACAGGCCTCAGAAG[A/G]AGGGAGAGGTAATTA	84182
rs546046669	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836893	GAAATGGAAATTTGG[C/G]TGTGATGTAGAAGAA	84182
rs546056756	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30789402	TTCGCCAGATTCTCT[A/G]GAAGGGACATTGTGG	84182
rs546067425	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30827224	GGAGGATTTTAGAGG[C/G]TTAGTACCAATGCCT	84182
rs546083098	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30796534	TTTAAAAAGCAGGGT[C/G]GAATACATGCATCTT	84182
rs546101612	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30867737	GGTCAGTTTCTGAGA[A/G]TGGCAAGCAGGAGCT	84182
rs546117041	snp	A/G	0.00557542	0.0525036	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30857660	TGTATTTTTAGTAGA[A/G]ACGGGGTCTCGATCT	84182
rs546146386	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30802617	TGGAAGGGAAAGTTA[G/T]GCTAATCTGTCTGTG	84182
rs546195795	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30885135	TTGTGTAGCACACAG[C/G]GGCTAAGAGGAGCCC	84182
rs546227811	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30844697	GTCTAGCCTGTAGAT[A/G]TTGGTGCCCAGGCTG	84182
rs546242147	in-del	-/GAAAGGGCCTTTAAG	0.0023933	0.0345097	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30879181	ATAACTGTATTTGGA[-/GAAAGGGCCTTTAAG]GAAATGATTAAGGTA	84182
rs546299466	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30868602	CTCAGGGCCAGTTCT[A/G]TACTCTCTCTGGGCA	84182
rs546323154	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30834932	ATTGTTCATACTACT[A/G]TCCGCATTTTTGTCA	84182
rs546367287	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30797231	GTCAGCTGTGAACAA[A/G]GCAGATTGAGTCCCT	84182
rs546370994	snp	G/T	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30825021	TGGGAGGTGGAGGCC[G/T]TAGCAGAGGGTCGAG	84182
rs546396375	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30830643	AGCATGAGGGTAACC[A/G]CCCCCATGATTCAAT	84182
rs546409696	in-del	-/TTTGA			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30847905	ACACCTGGCTGATTT[-/TTTGA]TTTGATTTTTCTAGA	84182
rs546495290	snp	A/G	0.00478085	0.0486577	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839506	AGCAAGAGCTGGGGA[A/G]TAAGACCCTCTGCTT	84182
rs546506928	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30881633	GAGCATGAGGCAGAG[A/G]TGCTGCGGCTGAGGT	84182
rs546528040	snp	A/G	0.00318978	0.0398085	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785497	GTCTTAAGGACTTGA[A/G]GGGTCCTGTTATGGA	84182
rs546532364	snp	C/G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30869547	CCTCTCTCCCGGGCT[C/G/T]GCAGGTGGCCACTTT	84182
rs546555694	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30832779	TCCCAAAGTGTTGGG[A/G]TTACAGGCATGAGCC	84182
rs546565974	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859519	ATTCTACATATACAC[A/G]TGTCCAGGGCTACCA	84182
rs546572604	snp	A/G	0.00318978	0.0398085	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30774521	ATTTCCTCCCTTTCT[A/G]TAGAAACCCCATAAA	84182
rs546620205	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30873588	CTATCAGGCTCCCCA[A/G]GGAGGGCGATTCTGC	84182
rs546657112	snp	G/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30865702	CTTAGGCCTTTGTTG[G/T]CTTGTGGCAACCCAA	84182
rs546664966	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782957	TGTAAATGTTAATCA[A/C]ATTTACAAAATGCCT	84182
rs546675850	snp	A/G	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30824331	AACTTGTTAATTTAT[A/G]ATCCCATTAATCCAT	84182
rs546683289	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30818085	GATGTTCTTTAGGGT[A/T]CAAATAAAACCCTTT	84182
rs546727500	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30837131	CTCCTAAGCCCTGGC[C/T]AGGTTGCAGTGAAGG	84182
rs546734857	snp	C/G	1.65616e-05	0.00287759	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785819	CCGCACAAAAGTAAG[C/G]CCATGCAGACGGTCC	84182
rs546738545	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30830731	ATGAGATTTGGGTGG[A/G]GACACAGCCAAACCA	84182
rs546747432	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30873797	ACCAGATGGGAAAAC[C/T]CGAACTTGCCTGAAA	84182
rs546826409	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30871700	CTTGAGCAAGACATC[A/C]CTTTTCTGAGGCTTG	84182
rs546855414	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30800208	TCACCCAACCCCTAG[A/G]TATTACAGTAAAGAT	84182
rs546898176	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852094	GAAACTCTTGGCTCC[A/G]TTTTCTCTCTGGAGC	84182
rs546902236	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30848112	CTTCAGTAAGTTAGT[G/T]TAGAAGTGTTTGACA	84182
rs546902956	snp	A/C	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30811664	GTTAAAGATCGAACC[A/C]TGACCTAATCAGTTA	84182
rs546956299	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30841038	GGACTTGTGCGCGTT[G/T]GTTTCTGAAAGCGGG	84182
rs546956487	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30835682	CTTTGATACCACCCC[C/T]GCCCACACAGGCCCA	84182
rs546978788	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30788335	TACCTTATCAGTTTC[A/G]CTTGATATGTCTTGC	84182
rs547026190	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850084	GTCCTGAGATGGCAG[C/T]CATTCCCGAGCACTG	84182
rs547063459	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30787774	ACTGTGGAAGGAGCC[C/G]TGCCTGGGTGACAGT	84182
rs547130975	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839605	CAGCAGGAGAGAGAG[C/T]AGTAGGAGGCCTTCA	84182
rs547135285	snp	A/C	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30873609	GCGATTCTGCTGGTC[A/C]ATGGACCACACTGAG	84182
rs547149089	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30845118	GTGGGGGCCCAGGGA[A/G]GCCAGGAGGAAGGCT	84182
rs547155851	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30834727	TGCCTTTAACAGCAC[A/T]CAAGTCGCCTCTTGA	84182
rs547212381	snp	A/C	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30844281	CTTAGTTATGGAGCT[A/C]GCTGAAAAAGCCTCA	84182
rs547212867	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30799417	CAACCTGGAATCACT[C/T]CCAGCCCTGAGTATG	84182
rs547225042	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30805800	ATGAAGGGTACACAG[A/G]GACAGGGTGGCAGCT	84182
rs547300876	in-del	-/GATGGCCCCT	0.0023933	0.0345097	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30804123	TCTCCATTTTGGAAA[-/GATGGCCCCT]GATGCTGAGTTATGT	84182
rs547305348	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882403	CCAACCCTGTCCCCA[A/G]GGAGCCTCCAGGCTG	84182
rs547326644	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30808475	GTGGGTGCCCTTTTT[A/T]CTCGTTCTTTGTTTT	84182
rs547335321	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30834998	TTCCCACATTTTCCT[A/G]TCTTCTTCTGAGCCC	84182
rs547352838	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30868716	TAGTATCTCAGGGAC[C/G]TTCTGATGGTGGACA	84182
rs547362691	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30798050	CTGCTGAAGTGGAAA[A/C]ATCATAGAGTGTACT	84182
rs547365397	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836331	GGTCCTGGTTCGATG[A/G]CTTAGGACCCAGGCA	84182
rs547380714	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791067	GAAAAGACATTCCTG[A/G]GAGAGACATCACATC	84182
rs547411154	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850104	CCCGAGCACTGCTGG[A/C]TGGGCCTCCCAGTCC	84182
rs547416253	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30874122	TTCTGGCCATTCCTA[C/T]GTGCTCCACTGTGGG	84182
rs547417990	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30881133	AGAATCAGCCTGGCC[C/T]GTGGCACGTACATAG	84182
rs547477691	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30796738	TTGTAGTTAATGTTT[A/G]AAGCTTTCTTTTTAA	84182
rs547478634	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30886911	ATGGTCATTTCCAAA[C/T]GAGACACACACAGTG	84182
rs547487972	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30787207	GATTTCAGTGCTGTC[A/G]AGATCATGCAGTCTT	84182
rs547587116	snp	A/G	0.00358779	0.0422022	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30809806	AAAGGGGGAAAAAAA[A/G]GGGGGGCAGAATTTA	84182
rs547602275	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30888317	TATTTGCCAATGTCT[A/G]AGGACATTTTTAGTT	84182
rs547605467	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30809139	TTGAAGGTGTTCTCC[A/G]TAACCCTATAACACT	84182
rs547642132	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30878765	GCAAGAGTTCTGAAA[A/G]CTCCATCCTCCTCCC	84182
rs547650602	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30802231	TTAGTAGGACCAGAA[C/T]AAGGCTGAGTGAGGT	84182
rs547657154	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30862461	ACACTGCACTCCAGC[A/G]GCGCTCCCTGCATCC	84182
rs547661253	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778083	TCCTGGTTTCCCCAT[C/T]TGAGAGTGAAGGGAA	84182
rs547674344	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850898	TTCTCTGATCTGGAG[A/G]CCTCAGGAAATAGCC	84182
rs547682610	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30821137	CCATGCTCCTGTTTA[C/T]TATGTCTGGTGTTTT	84182
rs547707310	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30884758	CCAAGCACCTCCCAG[C/T]GTGGGCCCAGGATTG	84182
rs547727462	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771032	CGTCAAGGCCCGCCA[A/G]GGTCAGTAGCGTTGG	84182
rs547756237	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30879168	TCAGAATGTATTAAT[A/G]ACTGTATTTGGAGAA	84182
rs547793322	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30846204	CCTTTCTACCCCCTA[C/T]TGCAGCTTTTGACCC	84182
rs547814479	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30883554	CCCTCTGTATTTAAG[A/G]GGAGGCTGAGGCTCA	84182
rs547821821	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30810292	AAAAAATTTATGCAA[A/G]AAATGTTGTATAATT	84182
rs547865012	in-del	-/A	0.00318978	0.0398085	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30880583	TCTCTCCCTGCCGTG[-/A]ATGAATGCTGGGTCC	84182
rs547890365	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	FAM188B, INMT-FAM188B	GRCh38.p7	7:30892524	CCCAGGAGAATGGAG[A/G]TGGACCTGGAGGGTA	84182
rs547897984	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30775681	TGGTGACCAGCCCCC[A/G]TCCTGAAGCTATCTA	84182
rs547902470	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30769863	AAAACCCAAGATCTT[A/G]TGGCTATTACTGCTT	84182
rs548010936	snp	A/C/G	0.000744959	0.0192856	synonymous-codon, missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778515	AAATGATCTTCGAAA[A/C/G]GTTTTGCATCTTGAA	84182
rs548012559	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853881	GAGGTAACCAGAAAG[C/T]GGCTTCTTGGGTGGG	84182
rs548023953	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30781067	AGGGGGAGGACTTGG[C/T]ATGCCCTGAGGGCCT	84182
rs548056321	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30780399	GTCTTTGACATTCAA[A/G]CTATTTTTATTCCCT	84182
rs548075605	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30829416	AGGCTTGAGTGCTGC[A/C]AACATTTGCTCCTTT	84182
rs548111307	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30860838	TCCCTACCCTTTCCA[A/G]TCAAGCTGGGCACCT	84182
rs548166698	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30787663	GTATGGGAGCCTTCC[A/G]TTAGTCAGAGCCACC	84182
rs548167518	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30851982	CAAGCTCTCCCTTTG[C/T]AGTCTTTTTTCCATT	84182
rs548232593	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30832213	GGGACCCAGGCAGAG[C/T]GTGTTTCAGGCCTGG	84182
rs548290891	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30855221	AAAATGGAAGATGGA[G/T]CAGTTATCAGGTAGC	84182
rs548369200	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30786966	CTGAGCCAATCAAAA[A/G]CAGGGTGTCTGTGTC	84182
rs548369667	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782918	CATCATTGGGATAAT[C/G]TGCCTTACTTAAAGT	84182
rs548374428	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30838153	GCCCATCATGAGGGG[A/G]GTGGGCGGGGACCTG	84182
rs548384567	in-del	-/TAA			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839868	GCCTAGAACATGGCT[-/TAA]TATACCCAGTTCCCA	84182
rs548396570	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30827358	CCGAGGTCCTCAGCC[C/G]TTTGTTGCAGAGCAG	84182
rs548429416	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30881041	AAAATAATTCCCATT[C/T]TTTCTTTAATCCACA	84182
rs548433885	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30801442	TTAACCTGTTCTGGG[G/T]ACCTCTCTTCTGTGG	84182
rs548447357	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30817473	AACTTACTGCTTCTC[C/T]AGCAGTTCAGTCATT	84182
rs548462421	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30833508	GGAATTATGGGAGCT[A/G]CAAGATGAGATTTGG	84182
rs548492210	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30884094	GGTTGGGGTTGTGAC[A/G]GGGGATGCAAAATGG	84182
rs548495497	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30800962	TGTTGCATAATTTAA[C/T]TCAGGGGACATTCAC	84182
rs548540048	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30824262	GGAGGCTGAGTGTGC[C/T]AATTCAGATCTGTCT	84182
rs548543662	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872543	TTATGTGCACTGATG[C/T]ATGTGCTCAGAGCTG	84182
rs548554871	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30777147	CTCAAAGTTCAGGGA[A/C]TGCAGGCCTATGGCA	84182
rs548558104	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30877990	TGGCCCCTTCCCTCT[C/T]CTTTAACACCACCTT	84182
rs548563204	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30813909	TCTTTTTTCATGATG[A/G]GGCAGTGTAGGGTGG	84182
rs548590649	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30813530	TGAACAGCTGAGGAA[C/T]CTCAGCAGAGGCAAG	84182
rs548615479	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30860957	TACACAAAGACAAAC[A/G]TGGATACACACAGAT	84182
rs548640467	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30776606	CTAGCAACTGGACTT[A/T]CGGACTAGTGGTCTG	84182
rs548651087	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30823541	ATGTATCATCTATCA[C/T]CATTGTTATATGCCC	84182
rs548652881	snp	A/T	0.00478085	0.0486577	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30830680	CCATCAGTTCCCTCC[A/T]ATGACATGTGGGGAT	84182
rs548671011	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30867280	TTTCAACTGCTCGGA[A/G]GTCTCGGTTTAATCT	84182
rs548698369	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30856597	TTGGCGGAAGGGGAA[A/G]CAGACCACAGACCAA	84182
rs548725847	snp	A/G	0.000121803	0.00780298	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859193	TGTGGCTCCCACAGA[A/G]GTGTGGGGCTGGGAA	84182
rs548726589	snp	A/C	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30829671	TCTGCCTAACTGATC[A/C]TAGAAGTAGCAGATC	84182
rs548764248	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30788445	AGATCTTCCAAATGT[A/G]GACACATCTCATTAG	84182
rs548812682	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30797968	GAAGCGCATCCACAT[C/T]TGTGGGCCCCTGGAG	84182
rs548822341	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872188	TGGTCACCTAGCGAG[C/G]TTTGCAACCTGGGTC	84182
rs548823199	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30804365	GTGGGGCCTTTTCCC[A/G]ATAAAGTAAACAGTT	84182
rs548824980	snp	C/T	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30797501	TCTGGACGCAAATGC[C/T]GACAGCAGTTGTGCA	84182
rs548905207	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30848922	AAGACAATAGTCATA[C/T]GCGCCATTGATTGAA	84182
rs548905892	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30838123	AGATGTAAAACCATG[A/G]CAGAGAGAGGGTGGG	84182
rs548952532	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30864434	TACTGACTGATTCCT[A/T]TCAGAAGCCCAGGCT	84182
rs548954091	snp	G/T	0.000798403	0.0199641	downstream-variant-500B	FAM188B, INMT-FAM188B	GRCh38.p7	7:30892801	GAAGGGGATATAGTA[G/T]TCTGAGCCTTGTTTG	84182
rs548967735	snp	C/T	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30874234	TGCTGGGGCTGGGCT[C/T]GCTCAAATTCCTCCT	84182
rs549009741	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30871042	CCCCAGGGTTGTGTG[C/T]ACCCCCCTGGGTCGT	84182
rs549022479	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30885080	ACAAGGCTGAGCCCC[A/G]CCATCTCCTTGAGCA	84182
rs549041012	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785413	TGGGCTTCGCATACC[A/G]CATGACTGTACTGAA	84182
rs549043686	snp	A/T	0.0023933	0.0345097	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30779150	CATGGCACCCTCTAG[A/T]TTTCCTGTTTTTGTG	84182
rs549073613	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30793932	GAAAAAGCATCCTTC[A/G]ACCCAGCAATTATTA	84182
rs549075652	snp	C/T	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30837087	TGGTCCAGTTGTCCC[C/T]ATTAGAGCAGCGCTG	84182
rs549095837	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30871378	ACAGAGTTTTCATCT[C/T]TCAGAGGGAGTTACA	84182
rs549109651	snp	A/T	0.104504	0.2033	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30841636	CAATTGGCCTTTTTT[A/T]AAAAAAAAAAATTTA	84182
rs549118850	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30835547	GCCCAGTGGTAGAAT[C/T]TATGTGCTTGTTCAG	84182
rs549185109	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30869403	AAGAAAGGGCTCTGA[A/G]TCTAAAAAGATGTTG	84182
rs549187530	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30780612	CAGCACAAAGCTCGC[A/C]TGATTCCAGGAAAGC	84182
rs549221121	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30880838	AGAAAGGATGAGTGC[A/G]TTGTAAAGACTGTCC	84182
rs549228161	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30802127	TGTATTCCTTTTTTT[C/T]TCACTCCAAGATGCT	84182
rs549248311	snp	A/C	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30868971	GTGAGTTTTCACCCC[A/C]TGGTCAAGCCCATCT	84182
rs549323365	snp	G/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30786724	CCAAGCCTTATAGTT[G/T]CATTTATTCTGCTTT	84182
rs549331047	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852758	GACATACATTTTTGT[A/G]TTTTGTAAAATATAA	84182
rs549345439	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30881818	TTAGGAGGTCACTGC[C/T]GTGGTGCAGGTTGGA	84182
rs549349338	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30811596	AGTAAAAACTAAAAG[A/G]CAGAAATGAAATCCA	84182
rs549355617	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30777370	AGCCCAGATGAAATG[C/T]GGGTGGTTGGTTTTG	84182
rs549362017	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30793209	TCCTTTGATATTTGC[C/T]GAGATTTCCTTCTAG	84182
rs549458032	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30799318	TGAGCCTGTAAACCA[A/G]GGTCCTGTGACTTTG	84182
rs549471408	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30834135	GTAGGGATTCTTTGT[A/G]GAGCCTCCATCCCCA	84182
rs549472267	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30826165	GTCTAAAGATCCTTC[A/G]CTTATTCTTATTTGC	84182
rs549478576	snp	C/G	9.61215e-05	0.00693192	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882348	CCAGCAGGAGCAGAT[C/G]CGGCTGACCATTGGT	84182
rs549479701	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30789823	TCTCCCCACCCTCCC[A/G]TTAATAACAACATGA	84182
rs549495545	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30844178	CAGGTTGAGTGAAGC[G/T]GTCTGACTTCCTGCT	84182
rs549516621	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30816902	AAATATTCCTTTTAT[A/G]TGTTGTAGGTCAACC	84182
rs549521303	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30798749	GTGATCCGCCCGCCT[C/T]GGCCTCTCAAAGTGC	84182
rs549521354	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30805721	AGAAAGTCAACTGTC[A/G]TGTATTGAGGAATGG	84182
rs549532782	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839022	CATTATTGAGTTTCT[A/C]TTTCATCAAATATAA	84182
rs549558916	snp	A/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850078	GGCAGGGTCCTGAGA[A/T]GGCAGTCATTCCCGA	84182
rs549571325	snp	C/T	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30849471	ATATTCGGCTGTTTC[C/T]CTTCCCTCTCATTCA	84182
rs549573752	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30878733	GAAGGGACCCACAAA[A/G]GAAAACAGCTTGACG	84182
rs549611738	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30779127	CCCAACCTGCTATTA[C/T]AGGCTTTCATGGCAC	84182
rs549650653	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30811156	TGCTGTTCATTCAGC[A/G]GAAAAGGGATGGACT	84182
rs549662641	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30816923	TAGGTCAACCGTTTG[A/G]GAACTGGCAACTGCA	84182
rs549681370	snp	C/T	0.000116155	0.00761996	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852322	AAACTTTGGCTTTGT[C/T]TGGGGACTGTCTCCT	84182
rs549694754	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30887657	CGTCCAGGAGGAACA[G/T]CTGGCCTGGTGGGGG	84182
rs549704114	in-del	-/T	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30793356	TAACTTCCTTTAGTA[-/T]TTTTTTTTAGCAGGT	84182
rs549732333	snp	C/T	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30796670	AGAAAGGAAATGACT[C/T]ACTTGAGCTTTTGCA	84182
rs549798469	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30886278	ACCCCTGGGCTGGAC[A/G]CCATGGAAGAAACAG	84182
rs549801180	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30813479	CCTCAGTGAATGCCC[G/T]CACCTGCTGGGTTTT	84182
rs549805952	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30795326	TGTGGTCATGAATTG[A/G]GAAGAGTTTTATCCT	84182
rs549871075	snp	C/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30878126	GCCAGGGCCCTTGCT[C/G]TGGCCTGGCCTGGCC	84182
rs549881187	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30838545	AACTTTGCCATCATG[A/G]TATGAACACAGCCAT	84182
rs549924687	snp	A/T	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30801687	CTCCAAAAATGGGGT[A/T]GATGACCCCTAAACC	84182
rs549940805	snp	C/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30843698	AGGTTGGGATCCCAA[C/G]GGGGTGTCTGGGTAG	84182
rs549944558	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30770931	ATGGCAGTCTCATTA[C/T]GGGAAAGCAGGCACC	84182
rs549983661	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30884267	TGGGAGGAGCGCCGA[A/G]ACATCCTCGACATGC	84182
rs550004615	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30784198	ACTACCTGGCTGGGA[A/G]GTGAAATACTTCTGG	84182
rs550005070	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30869821	TCCAGGCCCCTCGTG[C/T]TGCAGGAGGGGAGAC	84182
rs550005736	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30809350	CTCATTGTGAGCACA[A/C]CTCACCAGTTCAGAA	84182
rs550017147	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30800263	ATCACCTTAGATGCA[A/T]TGGATGCCCTGGTGA	84182
rs550021174	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836069	AACTCCTCTAAGCCT[C/T]AGTTTCCTCATCTAT	84182
rs550025562	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30881709	ACTATTTCTGCTCCA[A/G]CAAGGGATTTGGGAG	84182
rs550032719	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30807883	AGGAATTGCTCACTC[A/G]GGGAGCTCGGTTGTT	84182
rs550035086	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30867807	AGTGGTCAGGTGGAG[G/T]GGGGATAGCTGGTTG	84182
rs550039075	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30890574	ATTCAAAATATGCAA[A/G]GGGAAAATTTAGTCT	84182
rs550070706	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30769973	GGTTAAGGGCTGAAT[C/T]GTGTCTTTCAAAACT	84182
rs550083140	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30832046	GGCCCGAGGCCTGCT[A/G]TATGGTCCTAAACCA	84182
rs550112647	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30796039	ACATTCAGGGGGTCT[A/G]GGATTAGGATGTGGA	84182
rs550133684	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30807349	ACACAGAATTCTCAC[A/T]CCCATAGTCTCCCTC	84182
rs550191803	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30845760	GATGGAGGATGGGAT[C/T]GCACCCTCCAGGGAA	84182
rs550192635	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30805903	TGTTTGCACCAGCAG[C/T]AGAGACAAGAAATTC	84182
rs550218175	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30845269	AAGATGAACACAGAA[C/G]AGTACAGAGAGCAAC	84182
rs550274896	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30822003	CTCATCTCCTCCTCC[C/G]CAATATATATTAATC	84182
rs550330270	snp	A/C/G	0.000280612	0.011842	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850522	CAGACATTGTGTGGC[A/C/G]GGCAGGGGGCCGAGA	84182
rs550345641	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30862415	CCAGAGAGTAGTCCC[C/T]AGAACAGCCTGCTCC	84182
rs550366928	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30821915	AGAAGAGTACAATGA[A/T]TATCTGTAGACTTTT	84182
rs550381485	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30888265	GTGTTTTTACGGAGC[A/G]AGTGGTCTCAACGGG	84182
rs550400009	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30818591	CACAGACTTTTAGTG[C/T]GTCAGTGAGATTCAT	84182
rs550407322	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30779765	CCAATTCTATTGTAG[A/G]AGTGATGATCAAGCA	84182
rs550413378	snp	C/T	0.00318978	0.0398085	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30870951	CAGGGTCGTGTGTGC[C/T]TCCCAGAGTCAAGTG	84182
rs550420939	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30861240	TACACTGTGGCCTCC[C/T]CTTCCCCTCTCCTAA	84182
rs550431415	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30821418	CTTTCAGCTTTGAAG[A/G]TGTTATTTTATTGTC	84182
rs550441196	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30866066	TGAGATGGCAAGTCA[C/T]AGCCACTGAGCTGTG	84182
rs550477173	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30870265	TGGACTGCTTCTAAA[A/C]GCTCCAGGTGGCATA	84182
rs550487679	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828810	GCTCTGTCTGGGAGA[C/T]GGGTGGTCGGGGGCC	84182
rs550539534	snp	G/T	0.0130921	0.0798413	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828320	ACAAGAACTCGATTT[G/T]TGTGTGTGTGTGTGT	84182
rs550555537	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30863873	AGGATTTCATGCTTG[C/T]CAAGCTTTGCTGCTT	84182
rs550584004	snp	A/T	0.00795532	0.062565	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30793138	TATATTTATATATAT[A/T]TTATATATATTGTTT	84182
rs550589182	snp	C/T	0.00358779	0.0422022	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30888725	TTTTTAAAATGTCTC[C/T]GCTTTGATTTTCTAT	84182
rs550677724	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30860492	ACCACCTTCTCCCCA[C/G]GACTGGGTTTGCTCC	84182
rs550690158	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30805974	CGGAAGGGGACAGTG[A/C]TGACAATACCAGAGT	84182
rs550725211	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30825041	AGAGGGTCGAGCCGA[A/G]TTCTGCCACTTGGCC	84182
rs550760867	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30770242	GTGAGCCGAGATTGC[A/G]CCACTGCATTCCAGC	84182
rs550794425	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30864313	CAGCAACAAAATAGT[C/T]GATTCCTTTGTGCAA	84182
rs550854691	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30838012	GAAAATAATGAGTCT[A/G]TAGGAAAGGTCTGAC	84182
rs550881951	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30806639	AGGGCTCCTGTGCCC[C/T]TGGGCATGTCTTTCC	84182
rs550909980	snp	A/G	0.00358779	0.0422022	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30842650	AGACAGGAACAGGTG[A/G]TTACAGGGGACATGC	84182
rs550918217	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30871671	TGGGGGCACAGGCCT[C/T]AGAGCTGGGCACCCT	84182
rs550935219	snp	A/C	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30830150	CTCCTCCTCCACCCC[A/C]GTTCATTTTACTTTG	84182
rs550941656	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836564	TCACTCAAACCTTCT[A/G]CAAACTTAGCAATGT	84182
rs550943735	snp	G/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30830885	AAAGATTGGTTGGAG[G/T]TAATGGCCCTGTTGG	84182
rs550947467	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30772075	TTTGTAAGTTTTCCT[A/G]TTGTCTTGTCCCAGG	84182
rs550963361	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30787602	AGTGGTGTAGCCTTG[C/G]CTAGTAGCTCCAGAC	84182
rs551010510	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30774201	CCCTGAAGCTCCTTC[C/T]CCATCTAATTTCACT	84182
rs551028950	in-del	-/ACACACAC			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785294	CACACACACACACAC[-/ACACACAC]CCATTGGCACACCTG	84182
rs551045724	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30829557	CCCCTATTTAGAACT[C/G]TCTTGTGTGAGAGGT	84182
rs551063257	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30822715	CCACAGCTCACTGCA[A/G]TCTTGACTTCCCAGG	84182
rs551102867	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30888754	ATTGTAATTGCAAAC[C/T]GCTTCCCTCTGGTGT	84182
rs551116824	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30891624	CCTAGTGGAGAGCGG[A/C]TGGTCCAGATGTGTG	84182
rs551121073	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30834800	TCATCTCTCTCAAGT[A/T]TAAAGTTCTGCAAAT	84182
rs551162596	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30787913	TTTACTATATTTGAA[A/G]TTAAAAGTGAGAAGT	84182
rs551180815	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30865474	CACCACTGAGACTCC[A/G]CTTCCTTCCACTGAC	84182
rs551280514	snp	A/G	1.66457e-05	0.00288489	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882899	CTGGGTGACATGTGT[A/G]TGCCTCTCTCCTCCT	84182
rs551337890	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30863002	CCTGCTGCCCCCCTC[C/G]CCAGCCTGCCAATCC	84182
rs551388220	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30885479	ATCATGCCATTGCAC[A/G]CCAGCCTGGGCAACA	84182
rs551394888	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30869345	CACTGCCTTCAGCCC[A/G]TATGTTTCATGTAAT	84182
rs551413037	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30845193	ACTCCTAGGGACCAA[C/G]GGGTGGCTCTGTTCA	84182
rs551415053	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30846347	TCTTTCATCTGAAAC[A/G]CTTGGGTAATTTAGG	84182
rs551455230	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836531	TGGGGTGAATGAATG[C/T]GGGGAGGAACCCTCC	84182
rs551532117	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30797428	CCAGGAAAACCTACC[A/G]GAGAGGGTTACACTT	84182
rs551546863	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853600	AAGGAGTAATGCTGG[C/T]CCCTGGTTGGGGGCT	84182
rs551572151	snp	C/T	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30844550	TGTCAAGTGAAGACC[C/T]GGAAGACCAGGGAGT	84182
rs551572672	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30790687	TGACCTAAAGTGATA[C/G]ACCCGCCTTGGCCTC	84182
rs551585527	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30881143	TGGCCCGTGGCACGT[A/G]CATAGCTGGATAAAC	84182
rs551594075	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30803438	ACTTAGCACACAGAA[A/G]AAGTCAACTAAAAAT	84182
rs551630512	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30880375	AAGGAAGTGAATTTC[A/G]TCTCTGGAAAATGTC	84182
rs551674391	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30846282	TGGCTCCATGGGCAC[A/G]TCACAGTGGACAGGT	84182
rs551700069	snp	C/T	0.00318978	0.0398085	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30777615	CTGTAAAATTCTGAA[C/T]ACAAAGGCTCTGGGA	84182
rs551721492	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30792216	TCTGAATGTTAAACC[A/G]ACCTTACATCCTAAG	84182
rs551724313	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30887145	TCAGCTACCCCCACT[C/T]CCTGCGGAACCTCCC	84182
rs551733507	snp	A/C	0	0	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30795259	GTAGGCATAGGCTGC[A/C]CAAGTTCCAGCCACT	84182
rs551756217	in-del	-/AAAC			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828251	AAGCTAGGAGAGAGG[-/AAAC]AAACAAACAAAAAAC	84182
rs551795375	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30798702	ACGGGGTTTCACCAT[A/G]TCAGCCAGGATGGTC	84182
rs551795857	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30815679	ATCACTTTTCCTTCG[A/G]GAAGATATTTTTCTC	84182
rs551809234	in-del	-/T	0.00358779	0.0422022	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30793112	TTCATACATTTAGGG[-/T]TTTTTTTGTTTATAT	84182
rs551842025	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30881770	AGGCTAGTGGACAAG[C/T]TGAATTTGTTTGAGG	84182
rs551879310	snp	A/T	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30846871	CAATTCACAATAGGG[A/T]TCCTGCCCCCACGAG	84182
rs551921525	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30811057	AGCACCAGCCTAAAG[A/G]TCACTTCTTATCGAA	84182
rs551927873	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30801595	TTTCTCCTTCTGATT[C/G]CTGGCCTCCTGAAAG	84182
rs552017055	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859895	GTATCAGGTGGAACA[C/T]GGTCCCCAGCCTGCT	84182
rs552037603	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30810461	TTAAAAGGTTAAAAA[A/T]ACTTTTTTTGAAGGT	84182
rs552061281	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30823519	CATGAATTTTTTTCA[A/G]TATTTAATGTATCAT	84182
rs552071415	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30779036	TAACCCAGGTGCATT[A/G]GAGTTGGAAAAGCAA	84182
rs552087664	in-del	-/C	0.151001	0.229563	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853976	GTGGGGGCTCTGGAG[-/C]CCCCCCCGCCTGCCA	84182
rs552142210	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30868834	AGGCTGGGTCATCCA[A/G]GCATCCCTGGAGGCT	84182
rs552156568	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30871488	GGGAGGGTTTTCTGC[C/T]TCACGTGTGGCACAC	84182
rs552204887	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30801036	ACAAGTGCATCCCAA[A/T]CTCTCCCAGGTCCTC	84182
rs552243418	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30814378	ATAATCTTATTTCAA[C/G]ATTATGTCAACCTTT	84182
rs552256755	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30807852	TCTGTTAGAATTGTG[C/T]GCCCTTAAAAGGGAC	84182
rs552266120	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30807402	AGATCTCAAGTCACT[C/T]TGTAGCCTTGACATG	84182
rs552274662	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30842807	CACACTCTTATTCCC[C/T]CTCAAATTGTTTTCA	84182
rs552309571	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30889589	AGCAGTGAAGATGAA[C/T]GCTCTGATATGGATA	84182
rs552342383	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30833074	TACCCAGCACCATGT[C/T]TTTAAGTCCCATTCT	84182
rs552374306	snp	A/C	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30838684	TAGAGCACTGGCTCT[A/C]AAACCCGGCACACTG	84182
rs552408774	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30873017	GCATGGACGGGCTGG[A/G]CAGAGCTGCACATCT	84182
rs552414350	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30777180	ATGCCCAGGCCCCCG[A/G]TGGTTTTCAAATGCT	84182
rs552432415	snp	C/G	0.00318978	0.0398085	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30812974	TGGTCAGCGCTCTTC[C/G]TGGCGTCTGCCTTGC	84182
rs552447685	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30878233	TCACTCACTAGCAGG[C/T]GAAGCCTCTCACTTG	84182
rs552492282	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30819596	ATTTTCTATTATGCT[C/T]ACGGATTGAAGAGTT	84182
rs552541074	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771620	GGATCATCGGGGTCT[A/C]CCCTGAAGGCTTTGC	84182
rs552570614	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30825552	GAAGTTTCTGAGCAG[A/G]GGAAGGATGTGGAAA	84182
rs552578037	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30777856	AACCCCAGATTTTCC[A/G]TTGCTAGAGCATGTC	84182
rs552604329	snp	G/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30861690	CACAGCTCCTGGTGG[G/T]TACAAGCCGGGAATA	84182
rs552630085	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30821851	TGTTTATGTTTACCA[A/G]AATATTTTTCCAAAT	84182
rs552640279	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30890933	TGTCAGGAATCCTCG[A/G]CTTTCTGGATGTAGA	84182
rs552643118	snp	A/G	0.00318978	0.0398085	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30810598	GTAAAAACACGACCG[A/G]TTTTTCTTAAAGCAC	84182
rs552653585	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30844886	CCTAAATTGGACTCA[A/G]TAAGAAAATGCAAAG	84182
rs552655232	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30816447	TGTGCCAAGGCCTGT[C/T]GGGAGGGACACATAC	84182
rs552679026	in-del	-/AG			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875925	GTGATTGTGGGTCAC[-/AG]TGGCTGCAGCTGGTG	84182
rs552682257	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30846949	TGGCTCGTCCGCTGC[A/T]CACCTCCTGCTGTGC	84182
rs552760838	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30802898	CCATCCATTCATCCA[A/G]CAAACCATTCCACCC	84182
rs552786204	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30866886	CTCCTTGCAGGTCCC[C/T]CTTTTTCCGTCCTGC	84182
rs552798801	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30810120	GGCGGAGGTTGTGGC[A/G]AGCCGAGATTGCGCC	84182
rs552820739	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30827376	TGTTGCAGAGCAGGC[C/G]GAGGTGGGAGAAGTG	84182
rs552824369	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30822977	CAGTTTTAGTTTTTC[A/G]TGAAGAGAATGGGCT	84182
rs552851950	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30779279	TTTGTTCACTATTTT[A/G]TCCCCAAACATAAAG	84182
rs552864351	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30892385	AAAAATGGGTCAAAC[A/C]CATGTCAAGGGCCCA	84182
rs552868079	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30851239	TGGGGGCACGTTGGT[C/T]ACTGTAGCATATTGC	84182
rs552926922	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853168	AGGCCCAGAGCTGCC[A/G]TAGGGCCACCTGAAC	84182
rs552934434	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30846485	TCTCTTGGTTTAAGA[A/G]CCTGGCCAGGTGCCA	84182
rs552942379	snp	C/G	0	0	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30838864	AAACCCCTAGTCTTG[C/G]CTGTGGAAGATCAGA	84182
rs552952678	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30833705	AAGTCCCTTCCACCT[A/G]TTAGCCAGTAAAATC	84182
rs552954998	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30846745	GTTTTGTGGAAGACA[A/G]TTTTTCCATGGACTG	84182
rs552998695	snp	A/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30774359	AGGCCCACCCCTCCA[A/T]GTGTGCATGCCCTCT	84182
rs553029275	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30870198	CCTGCTCCCAGCTGA[C/T]GCAGGCTCTCGAGCC	84182
rs553067683	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	FAM188B, INMT-FAM188B	GRCh38.p7	7:30892843	GATATCCCACCAGTT[C/T]CAAAAAGAAGATGAG	84182
rs553094405	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872201	AGGTTTGCAACCTGG[A/G]TCAGGCAGAGCTGTG	84182
rs553141895	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30780576	ATTAATATCTACTAC[A/G]TAATAATTTTGACAT	84182
rs553142314	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30864536	TTTTGGCTCCTCTGT[A/C]CCAGCTGCATTCTCA	84182
rs553164955	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30772773	TCCTGGCTGCATGTT[A/G]GATATCAATTGACAC	84182
rs553181587	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30857424	GTTTTTTCTTCCCTA[A/G]GTTATTTCCCCAAGA	84182
rs553206745	snp	G/T	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30780917	AGACAAAATAGTTTT[G/T]GTTTTTAATCTCTTA	84182
rs553232261	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30848622	GTTTTCTCATGGTGG[C/T]TTTCATAGTGAACCG	84182
rs553244657	snp	A/T	0.00398564	0.0444627	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30856804	ACTTCCCTAGGCAGC[A/T]TGCAGAGCTGGTACA	84182
rs553249586	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30869039	CTGCTCCCTGGAGGG[A/G]CCCCCAGTGCAGGAC	84182
rs553288926	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30841177	GACCTGCCGACCTTT[C/T]GACTGCGTCCGGGCC	84182
rs553344410	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30798790	GGCGTGAGCCACTGC[G/T]CCCAGCCCTGCATCT	84182
rs553369253	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30817980	CTAGTATGTATATCA[A/C]CAGCATATTGGGTAT	84182
rs553399339	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30776858	AACAGAGCCTGGCAC[A/G]TAGGAGGTGCATGAC	84182
rs553406536	snp	C/G/T	0.00159649	0.0282165	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30805279	CCTGGAGGAAGGGGA[C/G/T]GTTGGGCAGGCAGTT	84182
rs553422790	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30834061	TGTTGGTGAATCTAC[C/T]ATTCTGGGGTCTGGA	84182
rs553466802	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30867138	TTACCAAAGGTCACG[A/C]AGTGCAGGTGGCAGA	84182
rs553481626	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30817279	CCTAGAGGAGCTTGG[C/T]TGAGGAGCTACAGGA	84182
rs553489666	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30786988	GTCTGTGTCCACCTG[C/T]GCTCTCACTTACCTG	84182
rs553562008	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30870420	CGAAGCGCTATGCTC[A/T]GCCATGAGTCACTCC	84182
rs553564775	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30838590	CAAATGGGCTTTGCT[A/G]TGTGCCAGTAGAACA	84182
rs553658857	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30789294	CTGCTTCACTGCCAA[A/G]GGCATTGCTGCAAAC	84182
rs553677655	snp	A/T	0.00517822	0.0506191	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30838310	ACAGCCGTGAGAAAG[A/T]AGAGGGGCTGCCTTG	84182
rs553761266	snp	G/T	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30790884	GACTGGAGCGACGGC[G/T]TCACCTGCTGCATGA	84182
rs553775401	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30878206	CAGCCTGGGCCATGA[C/T]GTCCGCAGCGTTCAC	84182
rs553784252	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30867567	GCAGTAATTGGATTT[A/G]ACCAGGGCCCTCTGA	84182
rs553799270	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30809070	TTAAGAAAAAAAAAC[A/T]GTGTACCCTATTCCT	84182
rs553811731	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785300	CACACACACACACAC[A/C]CCCATTGGCACACCT	84182
rs553834397	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30829208	TCTGCATCTTCACTT[C/T]TGTGTACATCTGTGT	84182
rs553847478	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30847001	CAGACCAGTGCCAGT[C/T]TGTGGCCTGGGGGTT	84182
rs553852994	snp	C/T	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30784490	TCTTCCCCTCAAATC[C/T]GCCCTTGCCCTAAGA	84182
rs553870548	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30834202	ATGAGGGCCCCGCCC[C/T]TGTAGCAAACTTCTG	84182
rs553878881	snp	C/G	0.0154538	0.0865337	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30820604	AATATATAAACTTAC[C/G]GTGTCAGGCTTCTTT	84182
rs553881897	snp	A/G	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30874203	TGGATGAGACAGAGA[A/G]ACCTGCCTGCCCTAG	84182
rs553891489	snp	C/T	0.00318978	0.0398085	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30834893	CCAATTCCCAACAAG[C/T]TCCCCCTCTCCATCT	84182
rs553914253	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30885810	ACCTTCTTCCTGGCT[C/T]CATTAGCTATCCCCT	84182
rs553968330	snp	A/G	0.0023933	0.0345097	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30873853	CTGCCCCTGACGTGC[A/G]TTATTTTACAGCAGA	84182
rs554016632	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30855972	TAAGAGGGGTTCCTC[G/T]TGCCAGGCCTGGAAA	84182
rs554048443	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30795351	TATCCTCCCTTAGGA[A/G]TTCAACCCACAGCAG	84182
rs554065587	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771389	GTTCTTGCCGCGCCG[A/G]CGCCGCCGTCGCCAC	84182
rs554078502	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30854842	AAAGGAGGCAGGTGA[A/G]GTCACCGGAGGGGCA	84182
rs554089575	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30827827	CCAGGGCAAGATTAC[A/G]ATTGTTACTTCAATC	84182
rs554097730	in-del	-/A			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30809784	TGGTTATCATCTTCG[-/A]AAAAAAAAAGGGGGA	84182
rs554123647	snp	C/T	0.00358779	0.0422022	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30801180	AGGATGTGGCATTTG[C/T]GGTTCATTGACTGTT	84182
rs554155583	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30793607	TGTATTTTTTGTAGA[A/G]ACGGGGTTTTGTTAT	84182
rs554158949	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30808847	ACAATGGCTGAGACA[A/G]CAGCAGCATAAACAG	84182
rs554168278	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30874338	TGGGGGAAGAGGGAA[A/G]TCACATGGGACAGAG	84182
rs554202029	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30891262	TTCTGAGTGTTTTTA[A/G]AAAATTAGCACCATG	84182
rs554222383	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30837468	TATTTACTCAGCATA[C/G]AAATCAAAGAGCAAA	84182
rs554237393	snp	A/C	1.65842e-05	0.00287955	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882983	CCCCTCGAGCTCTGC[A/C]TCAGAACCAAGTGAG	84182
rs554249521	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882571	AGCAGTGAGTGGCAT[A/T]AAGGGCGTTGGGTAA	84182
rs554255870	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30803025	AAACATCCATTCCAT[C/T]CAACCAACTAACCAA	84182
rs554300471	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30888335	GACATTTTTAGTTGT[C/T]ACAGCCCTGGGAGAG	84182
rs554332399	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840055	CCTCTTGTGGCCAAA[C/T]TCAGCTGGTCTTCAT	84182
rs554356091	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850597	CGTGGCTCATCGTCT[G/T]CTGGCAGCTGCCGGC	84182
rs554370533	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30809406	AAAAAAGGATGATTT[A/G]ATATTAACCACTGAA	84182
rs554382127	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30774709	TTGTCACAGTTGATT[A/G]TGTCCTTCTGCTTGT	84182
rs554406010	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30845486	ACTCCCTTTTGACTC[G/T]GAAATTCTAGGATTT	84182
rs554410466	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30808056	AGGCAGCCCCTTAGG[C/T]GGCTTAGGCCTGCCC	84182
rs554444062	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30891610	GCCAACCATTGGGTC[C/T]TAGTGGAGAGCGGCT	84182
rs554478020	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853092	TGATATCAGTGACTC[A/G]CCCATGGGGTGCAGC	84182
rs554493616	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30815234	CCTTCCCTTTTGTCA[A/T]GCCAAGGATGACTTT	84182
rs554494374	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30811899	TTGGAGACGTGAGTC[C/T]TGCCAAAGCTCCTGG	84182
rs554501324	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30831896	CCTTGCTTCTTTTCA[A/G]TTCGACATTTAAACC	84182
rs554523845	snp	G/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30787389	AGGAAATTAAAAGAT[G/T]TGGAGATGTTTAATC	84182
rs554578953	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30871183	GACAGACCTGGGACC[C/G]AGGCTCCCTGGTCTC	84182
rs554602264	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30831714	GTAGGAAATTCTGCA[C/T]AGGCTCCCAGAAAAA	84182
rs554603578	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30806089	TCTCTAATGAAAGAG[G/T]CAATTCTACTCAGCA	84182
rs554620585	snp	C/G	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30842301	CAGGATCATGCCCCA[C/G]TGCCTGCTCTGGAAG	84182
rs554677931	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30879863	CACATTTGAGCACTT[A/C]TGAAATTCTGATGCA	84182
rs554693984	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30807703	TGTTATCTATACATT[A/G]CAGACATTGTATAGA	84182
rs554711394	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30826719	CTGTGCTGCCACGGG[A/G]TAGGGTTACTTGCTG	84182
rs554733310	snp	G/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30841902	ACTTGTTCTTTGAAA[G/T]AAGCATTTGAGAATC	84182
rs554742073	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30813181	AACCAGAGAACCAGA[A/G]CCCTGTCAGAGGGCT	84182
rs554801070	snp	G/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30847692	GTGTCTGGCACATGA[G/T]AAATACTCTATATAT	84182
rs554822051	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852509	GGCTTCCTGTCCCAT[A/C]GAGGGTGTGCAGAGC	84182
rs554823789	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30826234	AGGATGTGGATATAA[C/T]TGAGGGCCGTTATTC	84182
rs554867528	snp	C/G	0.00398564	0.0444627	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30781457	GTTGGGGTGTAAAGT[C/G]AGTCAGTCCTGACTG	84182
rs554894034	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30874514	TTGGTACACCAAAAT[A/G]TGGGAGGCATGGGTT	84182
rs554935039	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30790044	GAGACCATATGTAAG[C/T]GGGCACAGGGCAAAT	84182
rs555006199	snp	C/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30832479	CTTTGCAAAGCCTGC[C/G]TATCAGTATTCTTCC	84182
rs555044681	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30770042	CCCAGCACTTTGGGA[A/G]GCCGAGGTGGGCGGA	84182
rs555079457	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30769648	AAAGAACCATTGCAC[A/G]TTGAGAGGGGAAATT	84182
rs555088112	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882129	GACAGAAAAATGCCC[A/G]GACCCCTTTCCCTGG	84182
rs555109731	snp	C/G	3.34851e-05	0.00409163	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782157	GTAAATATATATGAC[C/G]TTTCAGATGAAGATG	84182
rs555145535	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771952	AGTCAGGGTCCCACT[C/G]GGAAAGAACTTCTCC	84182
rs555150595	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30788170	GTGTATGAAGAAAAT[C/T]TAGCCTCACACAGAT	84182
rs555159818	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30809503	CCAGACCTAGGAGGA[A/G]CCCCTTCAGGACAGG	84182
rs555172475	snp	A/C	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30815411	CACCCACACCTGGGA[A/C]ACCTCATGCTGTGGG	84182
rs555187519	snp	C/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30860197	GAGGCAGGGTGAGTA[C/G]CCTTGTGGTGCCCAG	84182
rs555247121	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30865855	CCCTGTGCCTGCATC[A/G]TCTTCCCTGGACTGT	84182
rs555258300	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30856195	TCTTCCCAAGTGGCA[C/T]CACTTTCTAGACCCT	84182
rs555315897	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30810065	CCTGTAGTCCCAGCT[A/G]TTCAGGAGGCTGAGG	84182
rs555323047	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30862213	GAGCTAACCCTCCTA[C/T]CCCACCTGGAGCCCA	84182
rs555325153	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30818939	CTTCCTTTTCACTCT[G/T]AGTATTGTTTATTTA	84182
rs555344090	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30779512	TTTTTTAAAAAAGCA[A/G]TAAAATGATATCTCA	84182
rs555350692	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30851154	CCGTCAGAGTGGAAG[C/T]ATCGCTGTCCCAGCT	84182
rs555371626	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30886599	AGGACTGTGGCTTAC[A/G]CTTTTGCTGTCCCAG	84182
rs555390961	snp	G/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30863954	GGATGCTCAGGGTCC[G/T]GGGGTCAGGACAGCT	84182
rs555400843	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30790234	GGAATTTATAATTTT[C/T]TTTTTAATTTTGGAA	84182
rs555482108	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778656	CTTGAGGTTCTCCTG[A/G]CCTGTCACACTTGCG	84182
rs555482953	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30857220	TCCTTTTGGAGCGAC[A/G]TTCACTTTTCTGATT	84182
rs555496082	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30892227	CAGCTGAGCTGTGAC[G/T]GCTGAGTACTGGAAG	84182
rs555525565	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30857629	AGGCGCCCGCTACCA[C/T]GCCCGGCTAATTTTT	84182
rs555552213	in-del	-/CTC			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30772846	GGTCACTGAAAAAAA[-/CTC]TTAGAGAGGGCTTCC	84182
rs555552556	snp	G/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30792888	TCTCTGAGTTTAATT[G/T]GCTATTATTTTCTAG	84182
rs555558089	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30830988	TGCTAAAGAGCTGGA[C/G]AGCAAGTCACTGGGC	84182
rs555565183	snp	A/G	0.0023933	0.0345097	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778225	TCACTCCTTATCTGC[A/G]AAATGGCCTGAAAAC	84182
rs555602325	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30784415	GCCTCAGTTCACACT[C/G]CCATCCTCTTTTCCT	84182
rs555623547	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836357	AGGCACTTGTTCCAC[C/T]CTATGTCCATGCGTG	84182
rs555654680	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30873805	GGAAAACTCGAACTT[G/T]CCTGAAAAAGGCTGT	84182
rs555656762	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30797012	GGCTTGTACTGGCTT[C/T]GAATGCTGATTTTTA	84182
rs555669116	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839658	GGCCTTCTTAGGCTG[A/C]TCATTGAGAGATTCA	84182
rs555673984	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30846423	TCTCTAGATAAATGT[C/T]TTTTTCCTGCACTTC	84182
rs555689601	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30783869	AGATGGGAAAAATCT[A/G]GAAAATAAGCTCTTT	84182
rs555698889	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30835278	TGGATGGCAGCAGGC[A/G]AAGAGAGCTTGTGCA	84182
rs555705535	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30783155	CCTGGTTCTGTCTGG[A/G]GGTTCTGAGGGGAAA	84182
rs555719926	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30867627	CACAGCTGCCCTTAC[A/G]CTATTGATGTTGTCC	84182
rs555720449	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30858336	TAAGGATTAACTCAC[A/G]TAATTTTCACAACTT	84182
rs555740687	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785202	CCATCCACCCTCTTA[C/G]ACTCCGCTCAACTCC	84182
rs555745964	snp	C/T	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782371	GTGTGTGTGTGTGTG[C/T]GCATGTATCTATATG	84182
rs555780565	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30874497	GGGACCTTCCAGCCT[G/T]GTTGGTACACCAAAA	84182
rs555789143	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30866959	CCTAGCCCTCTCCTC[C/T]TACTGCTTTGAGAAT	84182
rs555801572	snp	C/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30866193	AGAGCTGGGAGGTCT[C/G]AAGACCCTCGGTCCT	84182
rs555803220	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872726	TGTCTTTATAGCCAC[C/T]CTTCCCTTTGCATCT	84182
rs555810041	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30794327	ACACATGTGCACATA[C/T]AATTCTTCTAAAGCG	84182
rs555815063	snp	C/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840603	TGTGGCCCAAGGTTA[C/G]TGTGTTGTAGAAGCA	84182
rs555859627	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30881260	CAGGGGGCCCTTGTC[A/G]CTTCTCTTCCCATTG	84182
rs555864573	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872363	TCTGTCCCTCAGAGA[C/G]GGAGAGGTCCTCCTC	84182
rs555867947	snp	C/T	0.00398564	0.0444627	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30860613	TGATGCCAGTCTCAG[C/T]GCCCCCATCCATGCG	84182
rs555960527	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30874936	CTCTGTACTATTTTT[A/G]CAACTTCTTTTGAAT	84182
rs555965579	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30887066	GGTGCAGACAAGAAA[A/T]TGAAAATGTAATTCC	84182
rs556013122	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30794616	CAGATCTGACTCCGG[G/T]AGCTGAAGGGACTAT	84182
rs556019637	snp	A/G	0.0023933	0.0345097	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30881224	GGAAAGTGCATGGAG[A/G]CCAGGCATTCAGGGG	84182
rs556032869	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30798246	GGTACAGTAACAATA[C/T]GATACTATAATCTTA	84182
rs556047880	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30879559	CCTCAGCCCGCACCA[C/G]TCTCTCCCGCAGGCT	84182
rs556058807	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30821140	TGCTCCTGTTTATTA[C/T]GTCTGGTGTTTTAGT	84182
rs556078507	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30838252	TGCGTGGGTTGATGG[G/T]AAATGAACAGTGAAC	84182
rs556090642	snp	C/T	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30842901	CCTGCTGGCTCCTCT[C/T]ATTGCACAGAGGCCA	84182
rs556093926	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30877427	ACCATCTCCCCTCCT[C/T]GTGGGCTTCTTGGAT	84182
rs556094411	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30797739	TTAATAGGGTCCCTC[C/T]GGCTGCTGTGTTGAA	84182
rs556096086	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30804788	CTGGCTTTTGGGGCC[G/T]TAGTCTTAATCATTA	84182
rs556100842	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30845536	AAAAAAAAAAAAAAA[A/C]GGGCAAGCTCTTCTG	84182
rs556102529	snp	A/C	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30887180	AGCTTCCATGCTGAC[A/C]ATTTTGCCCAGGCTC	84182
rs556167393	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30860326	AGGACAGTGGGGGCT[C/T]TGTGGCCTCGTGCGC	84182
rs556214657	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30833759	GATACAATGGGGGTA[C/G]AGGCAGTGGGAAAAT	84182
rs556236217	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30802451	TGGACAACCCTCAGT[A/G]TAGAACAATGATTTG	84182
rs556239956	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30834380	GCTGTACATTGGCCC[C/T]TTTTAGTCATCACTA	84182
rs556250784	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30808574	CACCCCACTAGGAAC[C/T]ATGCTGAAAAATTTC	84182
rs556293353	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30891087	CTCATACTTTGAAAA[C/G]CATTTATGAATTCCA	84182
rs556326632	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30833209	TTTCACGCTGCTGAT[A/G]AAAACATACCCGAGA	84182
rs556339368	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30794302	TCCTGTGAGTTCTTC[A/G]AGGGGAGACACACAT	84182
rs556344634	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30772181	GTGGGGAAGGAGCTC[C/G]CCGGGGGGTCTTGGG	84182
rs556390993	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30885034	CTGCCCTTCTCTGCC[C/G]TCACATCTGCTTAGT	84182
rs556419043	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30877144	GAGCCCAGGAATGTG[C/G]CTGGTGAGAAGCACC	84182
rs556420553	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30776691	GCTGAACAAATAGCT[A/G]GCCATCTAAAACAGT	84182
rs556426503	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30801096	GTGAAAGCCACGGGC[A/G]CACAGATGCCTCTCT	84182
rs556429001	in-del	-/C	0.00716266	0.059414	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30855128	GGCCTGGAGCAGGGG[-/C]CTGGGGGCCCCCTTT	84182
rs556431804	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30890392	GCCCTGGGCAGAGCT[A/G]GGAGGAGAATGCAAT	84182
rs556473423	in-del	-/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30857190	TCTTGCCTGTGGACC[-/T]TTTGCACGTGCTTCT	84182
rs556474233	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30815815	ACCAGCCTGAGAGAA[A/G]GGCAGGGAGGTGTGA	84182
rs556478233	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839844	GGCCAGCGGAGGCCA[A/G]TGGTTGCAGGCCTAG	84182
rs556493610	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30807653	CCACACCCTGGGCCT[A/G]GTAGTTAAAGATTGA	84182
rs556512359	snp	C/T	0.078151	0.181571	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30889643	CCAAAACCCAATAGA[C/T]TCCTCTGGATCTGCT	84182
rs556534901	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30858818	GGAGTCCCAGTGTGC[C/T]GCTGACAAGCTGTGT	84182
rs556560935	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30842896	CTGTGCCTGCTGGCT[C/T]CTCTCATTGCACAGA	84182
rs556565642	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30813795	TTTGCAAAGCTAACT[G/T]GGGTTTAAAGCAACA	84182
rs556632919	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30886322	GGCTCCTGCTCTCAG[A/G]GAGTTTGCCATCAGC	84182
rs556643700	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30811310	GTAATAGGAGTTATA[A/G]TAGTAATAGAAACCT	84182
rs556646270	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30826892	TGTATTGGCATTCTT[A/G]CTGTTATTTTAATAC	84182
rs556646917	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30861714	GGGAATAATGGCCAC[A/G]GCTGGTCCAACCGTA	84182
rs556673969	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30844788	AGAGGGTACCAGACC[A/G]GGTCAGGACCTGGAT	84182
rs556677933	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30841769	AATATTTCTAGTACT[A/C]CAGAAGCATCCTCTG	84182
rs556691171	snp	G/T	0.00318978	0.0398085	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30814446	CATTGTTTTTTATTT[G/T]TATCACGTCACCATG	84182
rs556708734	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30810691	GGTCCAACATTAAAA[A/G]TGGAATAAATATGTA	84182
rs556709611	snp	A/T	0.00835141	0.0640778	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30794120	TGCACATACTACACA[A/T]CTCTACACAGTGCTC	84182
rs556726455	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30844591	TGTCGGGGGCCTGGA[A/G]AAGAGAAGGGAGGTG	84182
rs556736765	snp	C/T	0.00398564	0.0444627	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30784903	GGTAGGGGGCAATAC[C/T]CATTTATGGCAGAGC	84182
rs556791548	snp	G/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30843868	AGGAGCTGCTGGCCT[G/T]TTGGGGGTCATCATG	84182
rs556821281	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30779386	TTCTACTTAAATTTT[A/T]AATTTGTTATGAAGA	84182
rs556823073	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782373	GTGTGTGTGTGTGTG[C/T]ATGTATCTATATGCA	84182
rs556847592	snp	A/G	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30817134	CCACTGAGCTCCCAG[A/G]AGATGAAGACACTGA	84182
rs556851288	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30887469	TTCCTGTGAGCCACA[A/G]TGGCCTCTGGGCATG	84182
rs556877269	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30888976	AGGAATTTGTAACTT[G/T]GGAGCTCATACGAGG	84182
rs556911539	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836373	CTATGTCCATGCGTG[G/T]AACTTTCTAGTGGAC	84182
rs556916969	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30858190	GGGATGGTGTTTCTC[C/T]GGGGAGCAGAAGTGA	84182
rs556936141	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30808138	GGTAGGCAACTGCCC[C/T]GGTGGAATGCCTTGC	84182
rs556944019	snp	G/T	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30842403	GCTCAACACAGTCCT[G/T]TATGCTCAGGAATGC	84182
rs556944100	snp	C/T	2.5621e-05	0.00357908	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853490	TACTCCTGTGGGATG[C/T]GCGTCACTAAGCCTT	84182
rs556950398	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30798821	TACTTTCTATCAGGC[C/T]AGTGGTGTTTCTTTG	84182
rs557016505	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882063	TCCCAGCATCAGACA[A/C]AAACGTGATCTTCAG	84182
rs557028968	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30887928	AGCTGCTCCTCATTC[C/T]GAATGGCTGGAGCAC	84182
rs557047521	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30812625	TGTTACATGGGCATC[C/T]GCAAGCTCTTGCACT	84182
rs557068826	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30816183	ACCAATTGCGTGCCC[A/G]GGTCTCATATGCCAA	84182
rs557090932	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30825516	ATTTGGCCCTTGTCC[C/T]GCGGTCTGCAGGAAG	84182
rs557116807	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30775286	CTATAAATTGAGGGT[C/T]CCCACAACCCCCTCC	84182
rs557157993	in-del	-/A	0.402277	0.198272	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30810343	AATGTAAAACTATTG[-/A]AAAAAAAAAAAAAAG	84182
rs557161753	snp	C/T	0.00318978	0.0398085	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30818882	TATTCATACTAGTTT[C/T]TTCTTACTGAAAAGC	84182
rs557173587	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852476	GCTAGAGCTGGCTTT[A/T]CGGCCAAAAGGCTGA	84182
rs557173659	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30846652	GTGGGTGCAGGTTCT[C/G]ACGCAGGCACATACA	84182
rs557200176	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30862460	CACACTGCACTCCAG[C/T]GGCGCTCCCTGCATC	84182
rs557222786	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30867227	AAAACAGTTGATATC[C/T]GCTGTATCCAAATCC	84182
rs557272419	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30823773	GGTACATCATTTCTC[A/G]TGTGTTTAAGAGTTT	84182
rs557309799	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850633	GGCTGTGTATGCTCC[A/T]ATCCTTGGGTCCTTC	84182
rs557316790	snp	C/T	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778132	TTACATTTTTTCTTT[C/T]GTTTAATTTTAAAGC	84182
rs557345350	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30889041	TTGAAAAGATAGAGA[C/G]GGGCGGGGTGAAGGG	84182
rs557362607	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30793593	CCTGGCTAATATTTT[A/G]TATTTTTTGTAGAGA	84182
rs557402928	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836841	ATTTTGGTGTTTCTG[C/G]CCCAATCCAGCTCAT	84182
rs557407290	snp	C/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30774854	TTAGTTTATGGCTCT[C/G]TTCTCTTCTTCTTTC	84182
rs557471711	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30861428	CCTGTTTTTCAGAGG[A/G]GGAAGCAAGGCTGAG	84182
rs557477918	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30829071	AGAAAACAGTTCTCA[C/T]TCAAAGTATCAGTAT	84182
rs557478851	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30818121	CCTTGAGCATGCTAA[G/T]AATTATTTTTAAAGA	84182
rs557553212	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30834310	CACCTGCAGGCTCAA[C/T]ACCACATGGTAGCTG	84182
rs557631100	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828614	CATCGCTCTTAACAG[G/T]CTTCTCTGCCGTTTA	84182
rs557646845	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30871169	GCAGAAGTGGGGGGG[A/G]CAGACCTGGGACCCA	84182
rs557665652	snp	C/T	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30833894	TCCTTTGACTCCATG[C/T]CTCACATCTAGGTCA	84182
rs557679102	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30786061	GGGCTTAAGGCACGC[C/T]TGGGTTTATTTGGGG	84182
rs557686217	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30822590	ATCCAGGATCCATTC[A/G]AGGTTTGCCCATTGT	84182
rs557693199	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771875	AGCAATCCTAGCGCG[A/G]GCGCACAGCGGGCAG	84182
rs557700387	snp	A/G	0.00318978	0.0398085	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785512	GGGGTCCTGTTATGG[A/G]TCATCATCTCTGAAT	84182
rs557711929	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30876240	TGTATCACTCCAGTC[G/T]CTGCCTCCATCCATC	84182
rs557722430	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30829547	GAAAGCAGTGCCCCT[A/G]TTTAGAACTCTCTTG	84182
rs557735126	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785060	TGTGCTTATTCTCAC[C/T]GTCTCTTGCCTTCTT	84182
rs557757129	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30815371	GGCTGCCAGGAAGCC[C/T]TAATCAGAGGCAGCC	84182
rs557757480	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30869595	TCATCTTTTCCTTGT[A/G]AGTGTGCATCTTTGG	84182
rs557805963	snp	C/T	0.00398564	0.0444627	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30817176	CCTCTCCCTGGAGCT[C/T]GGTTTCCTTGTCTGT	84182
rs557823974	snp	C/T	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30823178	GGATCACTCTGTTAA[C/T]GTGGTGTATGTCACT	84182
rs557847980	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30867951	CTCTGGCTTTCTAAG[G/T]GAAGACACAAGCTGA	84182
rs557853410	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30874392	CAGCTCTGGCCCTAA[A/T]GGGCTGTGTGGCTTG	84182
rs557869355	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30814674	TAGAACATTTAACAC[C/T]CTTAGAAGGTCATAG	84182
rs557871311	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30784356	CACCCAGAGTGATAG[C/T]AGGCACTTTCCTTCT	84182
rs557913160	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30862804	CGTGTGGCTAACCCA[A/G]CCTGTGCCTTAGGTT	84182
rs557956775	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785556	TACTGGTCTTATTTT[A/G]TAGGGCAGACTTGCC	84182
rs558029808	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30880017	TTGATTATTTAATTA[A/T]TGTGTCATCCCCATC	84182
rs558038770	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30877916	AACTCCTGACCTCAA[A/G]TGATCCACCCACCTC	84182
rs558061604	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30824806	CTCAAGTGATCATCC[C/T]GCCTCCACCTCCCAG	84182
rs558074342	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30873233	ACTCTTCTGGCTGCC[C/T]GGGGTGGCCTCACTC	84182
rs558077171	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840197	AGCCCCGTGATGCCT[A/G]CAGAGATGAGCTCCT	84182
rs558086479	snp	A/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872855	AGGGACCTTTTCAAG[A/T]TGTTACCTAGTGAGC	84182
rs558100087	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30797237	TGTGAACAAAGCAGA[A/T]TGAGTCCCTGCCCTC	84182
rs558101204	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30788507	TCATTGATGTCACCC[C/G]CAGCTCATCCAAGAA	84182
rs558117373	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30789586	AGTTTGAGTCTCCTC[A/G]GGAATGGTGACTAAT	84182
rs558138208	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30794557	TGAGATGTTAGGCGG[G/T]GTGAGTATCTGTGCA	84182
rs558138312	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30788166	TGAAGTGTATGAAGA[A/G]AATCTAGCCTCACAC	84182
rs558145685	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30830379	TTCTGTGATGGGTTT[C/T]TGTATTAGTGTATTC	84182
rs558161357	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30803099	CCCCATCTTTAAGTC[A/G]TCTGGAATGTTGCCT	84182
rs558179334	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30885867	GCGAGAACTTTGCTG[A/T]CACCAGCTGCCTGCC	84182
rs558186528	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30775446	GTGGAGGGTCATGGA[A/G]CTTCTGTGCCGTCTT	84182
rs558203056	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30830014	TGAAGGATAGGAGGC[C/T]ATGGAACCCAGTCAC	84182
rs558205198	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30795435	GTCACATGGCTTCAA[C/T]CATGGAGCCGTGGGA	84182
rs558207007	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30835752	AAGCCCTCAGCTACC[C/T]TCTGGAGTTCACTCT	84182
rs558216546	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30827333	GACAGACGGGATAGG[A/C]AGGGTAGAACCGAGG	84182
rs558234070	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30877037	CTCTGGATGATACCC[C/G]CAGCATGCCAAAAGC	84182
rs558243894	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30797709	GCAGAGACATGCTGT[G/T]ATCTCACTTGTGTTT	84182
rs558271098	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30802705	TTTAGTTTGCCTGTT[A/G]GCATTCATTAATTTA	84182
rs558317292	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30835230	GCCTCACAATCATGG[C/G]AGAAGGCAAGGAGGA	84182
rs558330447	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30783309	CTACCTTTGATCCTC[A/G]TGTCTCCTTCTAAGA	84182
rs558366545	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30880582	CTCTCTCCCTGCCGT[A/G]AATGAATGCTGGGTC	84182
rs558385510	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30800598	AAAGGAGTGGAAGTT[C/T]AGGGAGCAGTTAAGG	84182
rs558427790	snp	A/T	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30886497	TTTGGGCACCCCCTG[A/T]TATCACCTCTTCTTT	84182
rs558465862	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30866895	GGTCCCTCTTTTTCC[A/G]TCCTGCGGAGCCTTC	84182
rs558475327	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30848325	GGGGTGAGATGGAGC[A/G]AAACTGCTGGTGGGG	84182
rs558495925	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30781673	TTGGAGCAAAAAATG[A/C]AGAGGAAATTTGCTT	84182
rs558499778	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30806763	CTAGGGGAAGGTGGG[C/T]CTGTTTGAAAGCTCT	84182
rs558500499	snp	G/T	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30892124	TGGGTCAGCATGACT[G/T]CAGAAGCATCCAGAG	84182
rs558549260	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30865388	TTTCAGCAATGTCTC[A/G]AGAGACCAAGGTGAC	84182
rs558549946	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30833054	ATTTGGTTTCTTACT[C/T]TCTCTACCCAGCACC	84182
rs558604163	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30873922	GGACACAATAAGTCC[C/G]CTTTGGTATCTCCCT	84182
rs558604300	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850791	TCTCATGTTGGAAGG[C/T]GTGGTCTGTCTGCCC	84182
rs558607280	snp	A/C	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30856101	GCTGGAGGATGCCCC[A/C]ACCTCTGCCTCCCAT	84182
rs558608720	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30871666	GGGGGTGGGGGCACA[A/G]GCCTCAGAGCTGGGC	84182
rs558609777	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30838196	TCTGAGGGCCTGTCC[A/G]TGGGGAAGGGATTGA	84182
rs558634798	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30807784	CCGGTGCATGCAGCC[C/T]GCAGTCACGTACCCC	84182
rs558711123	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30801884	AAGATGAGTGATCTT[A/G]TATTGTCCATCTGTG	84182
rs558722337	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30837691	TATGCTTGGGGCAGA[C/T]CCCTCAGGCTCCTAA	84182
rs558726941	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30841982	TGCATTCCTGGGAAC[A/G]ACACTGTTCACTAGG	84182
rs558780165	snp	C/T	0.0023933	0.0345097	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30847778	AGGGTATCACTCTGT[C/T]ACCTAGGCTAGAATG	84182
rs558807570	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30806138	AAATTTATTCCAATT[A/G]AGCAAAGCTTTGTTC	84182
rs558849401	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30888381	ATAATGCACACCACG[G/T]TCTCCACAACAAAGA	84182
rs558894051	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30811986	GTCCTGCTACAGTCC[A/G]TTTAATGTTTAATAA	84182
rs558922210	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30835399	GGTTATCTCTCACTG[A/G]GTCCCTCGCACAGCA	84182
rs558932481	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30835057	CTCAGTTTCAAAGTC[A/G]CTTCCACATTTTCGG	84182
rs558946339	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30795548	ACACAGGCCATCAGG[G/T]TCAGGGACCAGATGA	84182
rs558956238	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30878363	ACCCATACTCAGGGT[A/G]TACCTGGGGTAAACA	84182
rs559035025	snp	C/T	0.00398564	0.0444627	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30826855	GCACAGTGTGTGGAA[C/T]GGTCAAGGGAGCCTT	84182
rs559041402	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30866557	GAGGCAAGACCAGTG[C/T]GTGAAAAGCAGTTGG	84182
rs559059392	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30834980	TCTAGGAAGTTTCAA[A/G]CTTTCCCACATTTTC	84182
rs559079893	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30820460	CACCACCTCTGTCTA[A/G]TTCTAGAACATCTTC	84182
rs559086306	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30849193	TCTTTTCTCCTGTCC[C/T]GGAAAAGAGGGACGA	84182
rs559112864	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30770653	TTTGTATGGCAGCCC[A/G]AGCAAAGGAATACAA	84182
rs559161828	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30874161	CTGCCTTCTTGTGTC[A/G]CAGGCAGCGCCAGCT	84182
rs559173185	snp	C/T			synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782087	CCCAATCCCTGCACT[C/T]TCAGTTCCAAAGAAA	84182
rs559175339	snp	A/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30804254	CCAGAAAATTCTACT[A/T]TGTTTTCTCTACTCA	84182
rs559201621	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30815520	AGGTCCAGTAGCCAC[A/G]GGCTAGTGTGCAGAG	84182
rs559214338	snp	A/G	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30891330	CTACAGTAACTTTTC[A/G]TTTTGCAACTGAACT	84182
rs559237364	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30854185	CTTTGAATCTAGATT[C/T]ACCCTTCAGTAGCTC	84182
rs559264434	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30874584	TTCTCCAAGTTCCAG[A/G]GTTGGCATGCTTGTT	84182
rs559364781	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30809155	TAACCCTATAACACT[C/T]CAGTACCACTTTGTT	84182
rs559375564	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778325	TCAAGTGTAAAGGTT[A/G]TATGAGAATTATCTT	84182
rs559404154	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30803293	CCCTACCTTTTTGAG[C/T]TTTGCTCAGAATTAT	84182
rs559419971	snp	C/T	0.00398564	0.0444627	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30797819	GTTAGGCAACTGCAG[C/T]AGTAGAAGAGAGCTG	84182
rs559437748	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30891395	TAGTTATACTCCGTG[C/T]TTCTTCAGGTTAAAA	84182
rs559456229	snp	A/G	0.00517822	0.0506191	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30846257	TCCCCCAAATTATAG[A/G]CTCTGTACATGGCTC	84182
rs559465346	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30809551	CCAGGTAATTGAAGG[A/G]AAAAAAAAAAAGCCA	84182
rs559490351	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30773305	CAGTCCTGAAAGATA[C/G]GTATAAGTATTCCCT	84182
rs559510324	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30891791	TTTCGTAAGAGACTG[A/G]TGTGTGGGTTTGTGT	84182
rs559528180	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30880260	TTCCCCCACCAGGAC[A/G]AAGTCCCAGACTGTG	84182
rs559530033	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30886738	CCTAATTCAAACCAT[C/T]CCAGACCCCATGTGT	84182
rs559541684	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30886141	GTGAGAGCCCAAGCT[C/T]CTGATAAGATGCAGC	84182
rs559611092	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30862964	GACTTTGATTAGAGC[A/G]GCAGAGGTGGGAGGG	84182
rs559636154	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30856223	CCTGATGGCAGTTTT[C/T]AGGCCAGTTGCCTTG	84182
rs559643747	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30830012	GGTGAAGGATAGGAG[A/G]CCATGGAACCCAGTC	84182
rs559649927	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30824014	GGTCAATTTGAACTC[C/T]ACTGACACTGGGTTC	84182
rs559661787	snp	A/G	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30779559	GCAAAGCAAAGAAGG[A/G]AAAATGCCCTATTTG	84182
rs559670821	snp	C/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30884157	AGGGGGCACAGCAAG[C/G]TTAGGGTTGATGCCC	84182
rs559672362	snp	A/C/T	5.38604e-05	0.00518915	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771583	CCCCCTCCAAAGCCC[A/C/T]GGAAGTGGCTCTAAT	84182
rs559678708	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30770796	TGGGCCTCAGCAAAA[C/T]CTTAGCCTTTCTGAA	84182
rs559698398	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30855670	GGAGCCTCCCCCTCA[A/G]CCTGTACCCCAGGGC	84182
rs559698439	snp	A/G	0.00358779	0.0422022	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30862279	GCAAGGATGGGAATA[A/G]CCCGGGCAGTCGTGG	84182
rs559721339	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30780955	GAATAGTAAAACTGT[C/T]CCGGGTTTTGTCTGA	84182
rs559750380	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30811515	GATTCTCAAAGTGGG[A/G]GAAGAAGGGAGGAGA	84182
rs559762120	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30770211	TTGAATCCGGGAGGT[A/G]GTTGTTCACTTGGCA	84182
rs559862726	snp	G/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30807831	TCACGACCCTCTCAC[G/T]CGGACTCTGTTAGAA	84182
rs559890202	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30775686	ACCAGCCCCCATCCT[A/G]AAGCTATCTAGGGGT	84182
rs559904048	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778986	TGAGTCTCCTGTGAC[A/T]TATAATTTAGGTAGA	84182
rs559920411	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30823398	TTCTACATTCATTGA[C/T]GGTATTCTGTAGAAA	84182
rs559934100	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30816842	GCCAGCAATTCTAGT[A/C]AGGTTTTCCACATCC	84182
rs559941556	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859844	TCCTAATCTCCCCTG[C/T]CTGACCCCTTTTGGC	84182
rs559959056	snp	C/T	0.00438332	0.0466095	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30884177	GGTTGATGCCCACCA[C/T]AGGAAAGCGAGCCCT	84182
rs559991171	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785226	CAACTCCCCTCACCT[C/T]CTTTTGTTCTTTCTT	84182
rs560008293	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30865622	GTGCAGACACCTGAA[C/T]CTGGAGGCTTAGCCT	84182
rs560065915	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30890517	CTCCAAATGACAAGA[A/C]ATCTTTCTGCTCATT	84182
rs560070763	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30810745	TTTAATATTAATAGC[A/C]CACTAATATAAAGGT	84182
rs560087207	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30798046	GAGACTGCTGAAGTG[A/G]AAACATCATAGAGTG	84182
rs560122053	snp	A/C	0.000795809	0.0199317	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791443	CTCCGAGGACACCCC[A/C]GCAGTGGACGGCAGC	84182
rs560125690	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30829806	TTTAAGATTTTGCAG[G/T]GAAAGCTGCTTGTGT	84182
rs560132826	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30854908	AGAGGCCTCAGGGCC[C/T]GTCCCAAAAGCATGG	84182
rs560185514	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30788296	CTTAATGTGAAATCT[A/T]AAACCATATCAGTGA	84182
rs560193818	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30871867	CAGAGGTGGAAGAGG[A/G]TTCCTCAGTCTACAC	84182
rs560206050	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853892	AAAGCGGCTTCTTGG[A/G]TGGGTTGGAGGGCTT	84182
rs560211141	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30790385	AAGACTGTAAGCAGC[C/T]TCACAGCAGTTAAGA	84182
rs560247503	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30789608	GTGACTAATGTCTTC[C/T]TCACTTTGTGGAGGG	84182
rs560267271	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782539	AGACCCTGTCTCTAC[A/G]ACAACAACAAAAAAT	84182
rs560278359	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30855129	GCCTGGAGCAGGGGC[C/G]TGGGGGCCCCCTTTG	84182
rs560306588	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30788767	GCAGCCTAGATGGTC[A/G]TGCAGTGCCAGCTGC	84182
rs560327526	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30820103	AGACGGGGTTTCACC[A/G]TTTTAGCCGGGATGG	84182
rs560343692	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30819488	GGATGTTTTGGATCA[A/G]ACATGTTAATTTAGT	84182
rs560383033	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30867331	AGTGGTTGAGATGGC[A/G]GGAATCATGACCTCT	84182
rs560387456	snp	G/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872381	AGAGGTCCTCCTCCC[G/T]CCTCTTGCCCCAGAA	84182
rs560390371	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30878604	AAGCCCCTCCAGGCT[C/G]ATGGTCATGGTGGTG	84182
rs560444346	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30873009	AATGCGTAGCATGGA[C/T]GGGCTGGACAGAGCT	84182
rs560453514	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30884479	GCAGTGGGGACAGGA[A/G]GTGACACTAGCCTTG	84182
rs560474425	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30794337	ACATATAATTCTTCT[A/G]AAGCGTGGGAAAGTG	84182
rs560498393	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30824970	AGCAGTAATCCAGCT[C/T]ATGCCTCTCTCTGGG	84182
rs560511863	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30777787	AGAGCAACTGCTGTG[A/G]TTGTTTTTCAAATAG	84182
rs560518944	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30834068	GAATCTACCATTCTG[A/G]GGTCTGGAGGACAGT	84182
rs560565717	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30824281	TCAGATCTGTCTTCC[C/T]CTTCTTAGAAAGCCA	84182
rs560656055	snp	A/C	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839419	TGAGCATTAGCTGAG[A/C]TATTCTGGACCAGCC	84182
rs560727892	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30890046	GATTGCCAAAAGGCC[A/G]TACAACCTGATTTTG	84182
rs560728087	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30781123	CCTGGCTAGTCTGCA[A/G]AATCACAGAGTGCCC	84182
rs560731332	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30843936	TGGGGGGGCCTGCCT[A/G]GCTGGACCAGAGGAG	84182
rs560733820	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30786178	GACACGTGGGGCCTT[A/G]AGCAGGCCTCCTTTC	84182
rs560830874	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30802109	ATTATGGAGAATCTT[C/T]CCTGTATTCCTTTTT	84182
rs560837218	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30805029	CCAGACCTTCTTCTC[C/T]AGGCAATAGAGAGGG	84182
rs560839268	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30798019	GTTTGGGGTGCACCT[C/G]TCTCTCTCCTCGAGA	84182
rs560844981	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30808228	GAATTGGCACTTGGA[G/T]TCCGGACATCTGAAA	84182
rs560853626	in-del	-/CTTCTT			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30877680	Cttcttcttcttctt[-/CTTCTT]ttttttttttttttg	84182
rs560877249	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30779659	TCCCTTCTCTCAGGA[C/G]GGGGAGCTGTGAGCC	84182
rs560890571	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30887574	GGCAGGGCTTTGAAG[C/T]GTGAGCCAGCGAGGA	84182
rs560895480	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30864111	TCTTGGCCTTCATTA[C/T]AGCAGCAAGTTCAGC	84182
rs560935487	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30837881	GACAGATGAATCCAC[A/G]CATCCTTTCTCCTGT	84182
rs560954814	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30863840	AAGATCTCGAATTGC[G/T]TCCGGTAAATCTCAT	84182
rs560969214	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30870079	TGATATGAAATGCAG[A/G]TGTTCCTCCCTTTTA	84182
rs560970377	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30807878	GGGACAGGAATTGCT[C/T]ACTCGGGGAGCTCGG	84182
rs561007168	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872638	GGAGTGATGTCTCAG[G/T]CATGGGCCAGGGGAC	84182
rs561037652	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30886857	CCCCTCCCACTGTTA[C/T]ACTGTAACCATCTCA	84182
rs561074045	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30792034	ACCTGCAGCAACATG[A/G]CCAGGCAGACGTGGC	84182
rs561130102	snp	A/C	1.65682e-05	0.00287817	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840806	AAGGCTGTGTCCTAC[A/C]GAAACTCCTGTTTGA	84182
rs561140173	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30846762	TTTTCCATGGACTGG[A/G]GGTGGGGGTGGGATG	84182
rs561216868	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30881571	GAATTTCATTCACCC[A/G]ACATTTACTTACCCC	84182
rs561217095	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30849737	CCAGCCCCAGCTGCT[C/T]TCTTGGGCTTTCTAC	84182
rs561222685	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840362	CGAGATGGTCAGGAA[A/G]GGCTTCTTGGAGGAG	84182
rs561227199	in-del	-/TT			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30868106	TTCTTATTCAGAAAC[-/TT]TTATACCACATGCCC	84182
rs561228456	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30806288	GCTTTAGAATTGAAC[A/G]GATTTGGGTGCAAAT	84182
rs561233857	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30860858	GCTGGGCACCTGTGG[G/T]GAATTAGTGTGGGGA	84182
rs561288088	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30812155	GTGGATTTGGCAGGA[A/G]AGCGTCCTTATTCTA	84182
rs561289151	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30817640	GGAGGGGCTGGGTCT[A/G]AAAAGCGGAAGCCCG	84182
rs561289160	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30825625	GGGTTTGAATCCTGA[C/T]TCTGGCACTTCTAAG	84182
rs561289414	in-del	-/T	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30851673	AATTCAATTTCTCCC[-/T]GTTTTACAGATTAGG	84182
rs561289465	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30794032	GCAGATCCAAGGGCA[C/T]ACAGACTGGCAAATG	84182
rs561302494	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30871402	AGTTACATTGGGGTG[A/G]CTAAAAGGAACCATG	84182
rs561310161	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30848062	AAAATCTTATTTGTT[G/T]CTACACTGAGAAGCT	84182
rs561336841	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30837098	TCCCCATTAGAGCAG[C/T]GCTGCTCCTGTACTG	84182
rs561344890	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30838078	CACCTGCTGGTCTTG[A/G]GGCTCACTCAAGGCT	84182
rs561372093	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853223	CAGCCTTTCACTCAC[A/G]TACAGGTATGGCCGT	84182
rs561404817	in-del	-/CAGTT	0.0111196	0.0737302	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30856215	TCTAGACCCTGATGG[-/CAGTT]CAGTTTTCAGGCCAG	84182
rs561408229	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30848563	CTCTGCTTTCCAGGG[C/T]CCCCTTAGTCCTTGG	84182
rs561408959	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882847	GGGGGCGGGTCTCGG[C/G]AGTGGTCAGCGCTGA	84182
rs561411854	snp	A/G	0.00318978	0.0398085	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30830693	CCTATGACATGTGGG[A/G]ATGATGGGAACTACC	84182
rs561413939	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30876648	CTTCTTGTTCCAGCT[A/G]CCATGGAACATTTTT	84182
rs561418799	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30844852	CGTTTGTGAACTAGG[A/T]ATAGTCATCTCTGGC	84182
rs561430384	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30807329	TGCCAAAGAAACCCA[G/T]CCACACACAGAATTC	84182
rs561475732	snp	C/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30888173	GCAGTGATGCCTCTG[C/G]GGGGACAGGGCCTTA	84182
rs561493256	snp	C/T	0.0023933	0.0345097	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30873595	GCTCCCCAGGGAGGG[C/T]GATTCTGCTGGTCCA	84182
rs561495667	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30877989	CTGGCCCCTTCCCTC[C/T]TCTTTAACACCACCT	84182
rs561500818	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30805772	GGAGAGCCTTTGTGA[A/G]AGAAGTTTAGAGATG	84182
rs561516949	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30834644	AATGGGGTTTTCTTT[C/T]CTATTACATTTCTTT	84182
rs561526056	snp	A/G	4.97014e-05	0.0049848	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859267	CCCAGTTTGAAGTGG[A/G]CCCCTATGGCTGCAT	84182
rs561530847	snp	C/T	3.32099e-05	0.00407478	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850417	TCTCAACCTTGTGTC[C/T]ACATGGGCATAAATG	84182
rs561531008	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839583	GTGGTGCAGGTGCTG[A/G]GATCCTCAGCAGGAG	84182
rs561569466	in-del	-/C	0.00953873	0.0683987	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30866160	AGCTGAGAAGGGGGG[-/C]CACACCCAGGCCACT	84182
rs561596527	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850091	GATGGCAGTCATTCC[C/T]GAGCACTGCTGGCTG	84182
rs561606806	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30811635	CAGCCCAGCGCCACA[C/T]CCTGGCTCTGGTAGT	84182
rs561610418	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30855419	CCTGATGGCATCCGT[A/G]TGTGGGATCTGGCCA	84182
rs561627837	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30821748	ATTTATTTGCTCCTT[C/T]GTGCAGTTTATCTCT	84182
rs561651922	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30849155	ATGCTGCCCACTGTG[A/G]TGGGCTGGGTTCTGG	84182
rs561690000	snp	C/T	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30820807	TGCCGTGAACATTTA[C/T]GCACATGTATTTGTT	84182
rs561695619	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30854006	AGAGGAGAGCTGTAC[A/G]TCCACTCCTGGCCAT	84182
rs561702163	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30886849	TCCCCTGCCCCCTCC[C/G]ACTGTTATACTGTAA	84182
rs561749321	snp	C/G	0.00478085	0.0486577	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30773139	CAGGTATACTGCTTT[C/G]TCATCGCCTTCTGCT	84182
rs561752199	snp	C/T	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30871499	CTGCCTCACGTGTGG[C/T]ACACCTCTGCTCACC	84182
rs561755984	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30802702	AACTTTAGTTTGCCT[A/G]TTGGCATTCATTAAT	84182
rs561812646	snp	G/T	0.0023933	0.0345097	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30837326	CCTCACCACTCCCGT[G/T]ACCAGAGGCTCCTGC	84182
rs561837597	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778868	CATGAGGCTATTTTT[A/G]GTAAGACTGTACTTA	84182
rs561837644	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30772302	ATACTGGGCTAGGGC[A/G]ATGGGTACTTGTCTT	84182
rs561871737	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30890584	TGCAAGGGGAAAATT[C/T]AGTCTTTACAGATAC	84182
rs561884835	snp	C/T	3.12798e-05	0.00395461	synonymous-codon, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771547	GGTCAGGGAGTTCCT[C/T]AGCAGAAAGGTAACG	84182
rs561942915	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30789501	ATCATATTTACTACA[A/T]CACTTCTGTATTTAA	84182
rs561967056	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30855603	TAGCTGCCCACTGAT[G/T]GACTGGGGTGGCCCC	84182
rs562050659	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30846169	GTAGCAGAACCTATG[G/T]TCCTGCAGCCCCAGG	84182
rs562112782	snp	C/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30889474	ATCAGACTCCACCCC[C/G]AAATAGTATCAGCAA	84182
rs562125425	snp	C/T			upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30770813	TTAGCCTTTCTGAAT[C/T]TCAGTGTCCCGTTTT	84182
rs562169153	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30883773	GGAGGGAGAGGCCTG[G/T]ATCCTGGTCCCTTCT	84182
rs562205883	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30823230	ACTTTCCCTTTTGCA[A/G]TTAATAAGTAATCTG	84182
rs562219970	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30830039	AGTCACGGAGAGAGT[C/T]CATGAAAGGAAAGGA	84182
rs562233749	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30781750	ATCACCTGCCTCATG[C/T]GTTGGATGCTAGTTC	84182
rs562261608	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30865525	CGTCCCTGGGAGCCA[C/T]CTGCTCCTTTGTCCC	84182
rs562306173	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30812849	CTGGACCTTTGATTC[C/T]ACCCCCATCGTGAGG	84182
rs562321666	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30784568	CGAAGGGCTTCAGAC[A/G]TTCCCTGCAGCTTTC	84182
rs562358315	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791044	TTAAGGGAAAGAGTC[C/T]GAGGTGGGAAAAGAC	84182
rs562366991	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30819302	AAAATTTTCTAATGC[A/G]TGGGTTATTTTGGGG	84182
rs562374487	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30864902	GGGCAGTGCTCACCC[C/T]GTCAGAGACCCTCTG	84182
rs562380078	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30797287	TGAGACGAGGCAGCC[C/G]ACAATAACACCAAAA	84182
rs562389035	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30861848	AGCCACAGGGATGTC[C/T]GGCAATTCCTGATGG	84182
rs562390084	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853815	TGGAAGCAGCCGCCA[C/T]TGGAATACAGGAGCT	84182
rs562405990	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859747	CAGCCCTGCAGTCGC[A/G]TGGACAAGGCTGGCA	84182
rs562413656	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30874105	ACACTGGTCAAGGGC[C/T]GTTCTGGCCATTCCT	84182
rs562437786	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30871282	ACTTCATTCGGGTCT[A/G]GGGGTTGCAATTGCC	84182
rs562450449	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30843208	GAATGAGTTATCCAA[A/T]CAGGGAGGGGAGGCA	84182
rs562496900	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30827859	TATCTTACCCTGCAA[A/G]GATGTTGAAGGAAAA	84182
rs562592323	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30775131	CTCCAGACACCAATT[A/G]GGTGTCGTACAATTC	84182
rs562593532	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30793782	GCCTAAATGCCTTTT[A/G]TTTTTTATGGAATTT	84182
rs562622268	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853535	GGAACAATGCTGTGA[A/C]CTGGAGTTGTTCTCC	84182
rs562627015	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859394	TGCTGCCTCGCTAGA[A/G]CCCAGGATGGTGCTT	84182
rs562630684	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30788199	ATAAGCAGCTGGAAA[A/G]GGGAAAGTATTTTAA	84182
rs562632443	snp	C/G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30835880	GGGGGCCTTAGCTAA[C/G/T]GGGGAAGTCACAGCT	84182
rs562670911	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30837037	TAGAGCTGCTTCATC[A/C]TGTCCCTGTGGGCAC	84182
rs562689540	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30832202	ATTTACTTCATGGGA[C/T]CCAGGCAGAGCGTGT	84182
rs562827202	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30807803	GTCACGTACCCCCTG[C/G]TTGCTCAGTTGATCA	84182
rs562829174	snp	A/C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30800939	CAGCGATTTAGTCTC[A/C/G]TTGCCCTTGTTGCAT	84182
rs562832963	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30797033	CTGATTTTTAGTGCC[C/T]CTTCTTAACTTTGCA	84182
rs562840439	snp	A/T	0.00993419	0.0697739	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30793139	ATATTTATATATATA[A/T]TATATATATTGTTTA	84182
rs562873276	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30889973	AGGATCCCAGGAACC[A/C]AATGGTTCAGGTGAT	84182
rs562879292	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30795088	CACCTCACTTGTGTT[A/G]CTCACAGCCCTCCGT	84182
rs562886240	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782797	GCAGGCTGGAAATCT[A/G]GAAACTCAGACAGGA	84182
rs562892262	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30860021	GCAGATTAATAGCGC[A/G]TGAACGGTTGTGGAA	84182
rs562892643	snp	C/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30807307	TCTAGGAATCAACCC[C/G]TGGATCTGCCAAAGA	84182
rs562908040	snp	C/G	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30774297	GCTGCACCATTCACT[C/G]TGCTCTCTTTAGTGT	84182
rs562909524	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30877924	ACCTCAAGTGATCCA[C/T]CCACCTCAGCCTTAC	84182
rs563005703	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30878449	TGGCTGTGTCCTGCC[A/G]GACCTCCATGGGCTA	84182
rs563015062	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30835486	ATATCAGAAGCATTC[G/T]CATCTAAGTTCAGGT	84182
rs563115920	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30804306	CCATGGGATTTCTTT[A/C]ATTTCCTGTTGAGGC	84182
rs563146719	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30842661	GGTGGTTACAGGGGA[C/T]ATGCACGGTGCTAAG	84182
rs563153638	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791914	AAAAAACTCAATGTT[C/T]TAAGAAAGTTTATGA	84182
rs563207622	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30841016	CCTGCGCAGACCAGT[A/G]TTAAGGGGACTTGTG	84182
rs563227411	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30803441	TAGCACACAGAAAAA[A/G]TCAACTAAAAATAGC	84182
rs563229052	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30810133	GCGAGCCGAGATTGC[A/G]CCACACACTCCAGCC	84182
rs563240419	snp	C/T	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30883466	CCGGAGGAGCAGCTC[C/T]GCCACTCTGAACACT	84182
rs563242693	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30813343	TGTGTTAAAGTGTTC[A/G]ATCCCCAGGTCCTGA	84182
rs563248781	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30881414	ACCTCAGTGCCCTGC[C/T]GCACCCTGAATTTCT	84182
rs563271789	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	FAM188B, INMT-FAM188B	GRCh38.p7	7:30892422	TTTGTTCTACAGCTG[C/T]AAAGAGCGTGATGTG	84182
rs563272150	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30793484	ACAGTGGCGCAATCA[A/C]AACTCACTGCAGCCT	84182
rs563292990	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30809712	TAGTAACTTCTAATC[C/T]TGTGGCCTTAGACAA	84182
rs563311590	snp	A/C	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875973	GCCTTCTCAAGGGAC[A/C]GGAACTTGAGGTCTT	84182
rs563349387	snp	A/G	0.000116239	0.00762274	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791485	CAGGATGCCCTTGAA[A/G]CTCTACTTGCCTGGT	84182
rs563372233	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30869352	TTCAGCCCGTATGTT[C/T]CATGTAATGGGCTTC	84182
rs563382797	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30874668	GTAGCAAGACAACAG[C/G]AGAAGCAGAGCTAGA	84182
rs563405557	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30845720	TGCCCACCACATCTG[A/G]TGGGGAAATGGTTCT	84182
rs563406644	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30797912	TATACATACATACAG[A/T]CATACATCAGCAGGG	84182
rs563443987	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30887898	GGTGAGGGATACCCA[C/T]GTGGCTCATCCTAGA	84182
rs563480816	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30886196	TCTTGCTCGGTAGGT[C/G]GGGCTGCAGGGTAGG	84182
rs563481906	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30773867	CACAGTCCCTCGGGC[C/G]TACCATAACCCACCT	84182
rs563492244	snp	A/G	1.66685e-05	0.00288686	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840725	CTCTGCCCCAGGCCA[A/G]TTCTCACTGGCAGCA	84182
rs563504321	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30846070	TCCAGGAAGTCCTCC[C/T]CTCACTTCCACTTCC	84182
rs563505090	snp	C/T	0.00358779	0.0422022	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882837	GGGACTAGAAGGGGG[C/T]GGGTCTCGGGAGTGG	84182
rs563526168	in-del	-/G	0.00318978	0.0398085	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30856326	ATAATTGTAATAAAA[-/G]TTTTAAAAAACAAAA	84182
rs563526926	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30842081	TTAGGGTTCAAGTGA[A/G]GGTGGCTTTTCATGC	84182
rs563560573	snp	A/C	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30824903	CTTTCCACCAAGCCA[A/C]GGATTCAGTTATTCA	84182
rs563583808	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30886772	TGCGCTTTGCTGTGA[C/T]GCAAACCTCGGCCTG	84182
rs563637026	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30774421	CACCATGCATTTCCC[A/T]CCTCTACTAGGTTAC	84182
rs563645838	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30806222	TTTGAAACTTGGCTC[A/G]CCATCTTTCACATAT	84182
rs563673266	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30799117	TTGCAGTCTGCTGAG[C/T]AGACCTCCAGGCCTC	84182
rs563692148	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30817507	GAGAGCTGTTGAAGT[A/G]ATGGGGGTTATACAG	84182
rs563703333	snp	C/T	0.0154538	0.0865337	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30857563	CTGCAAGCTCCGCCT[C/T]CCGGGTTCACGCCAT	84182
rs563705986	snp	A/C	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30841545	TTCTTGAGGAAGTGA[A/C]CTGCCTCTCTTTCCC	84182
rs563711712	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30878728	TTCATGAAGGGACCC[A/C]CAAAGGAAAACAGCT	84182
rs563756327	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30805640	AGGTTGGGAGGTCAC[C/T]GGGCCTGGTGATGGC	84182
rs563764159	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30888465	TGGCTGGCTGTCAGC[C/T]GCCTCCTGCATTAGC	84182
rs563780887	snp	C/T	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850339	TGGCCCCTCTGCAGG[C/T]CAGAGAAAGAACAGG	84182
rs563786431	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30864067	CTGAGAAGGTCCAGT[A/G]GGGGTGAAAACCTTT	84182
rs563787573	snp	A/C	0	0	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882317	TTGACTTGTACTACT[A/C]CGATGGCCTGGCCAA	84182
rs563788031	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30864619	CAGCCTGCTGGGTGC[C/T]GGGTGCCATTCCTGG	84182
rs563801748	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30888099	ACCTTTTTCCCCATG[A/G]AAAACACTGGGTCCA	84182
rs563897516	snp	A/G	0.00318978	0.0398085	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30802130	ATTCCTTTTTTTCTC[A/G]CTCCAAGATGCTTTT	84182
rs563903517	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30770267	TCCAGCCCGGGCACC[C/T]GAGCGGGACTCTGTC	84182
rs563910557	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30864779	ACAGGTATCTGAGAA[C/T]AGGAGAGCAGATGTG	84182
rs563912369	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30773985	CAGTAAAATTCCACT[C/T]GTCCTGCTCTACACT	84182
rs563930637	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30816892	AGAGAGAAAAAAATA[C/T]TCCTTTTATATGTTG	84182
rs563963287	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30857821	TTTCACCAATACAAT[C/G]TTTTTAAAAAGACTA	84182
rs563964159	snp	C/T	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30779618	CGTCTAGCCTCTCAG[C/T]GTCCAGCTTTAAACC	84182
rs563968758	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30844128	GTAGCCCACCCCTAC[C/T]GGCTGCTGCCCCATC	84182
rs563984238	snp	C/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30854495	AGACCCGCGACCTCT[C/G]AGACCCCCACTACGA	84182
rs564000826	snp	A/C/T	3.36634e-05	0.00410253	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785699	TTGCTATCTTTGTTA[A/C/T]TGATTCCTTTTGGGG	84182
rs564028528	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30863684	CGAGTGCTGCCGACC[A/G]CTGCCTGCCTGGCCA	84182
rs564039814	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30809027	AAATCAAAGAGAGAA[A/G]GAAAGAAAGAGAGAG	84182
rs564043032	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30824158	GAGGTTGGAAAGTCC[A/G]AGGATGGGAGGTCAC	84182
rs564071628	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30837421	AAACTCCTAGGGACA[A/C]AGCTGACTTCCTTCT	84182
rs564145040	snp	C/T	0.00358779	0.0422022	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30820152	GTGATCCGCCCGCCT[C/T]GGCCTCCCAAAGTGC	84182
rs564152180	snp	C/T	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30808281	ACTTGCCCACTCCAT[C/T]TGAGTGGAAGCGTGG	84182
rs564162385	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30846598	TATCTGGTAAAGGCC[C/T]GGGTGATTCAGACGC	84182
rs564183989	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30860455	CTGGCGTGGACTCAC[A/G]TGCATGGAGACCATA	84182
rs564212626	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30813970	ACTTGATCTTGCTCT[A/G]GCCAAACCAGGGCAG	84182
rs564233869	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30784542	AGAGTCTGGCCATGC[C/T]GCTATCCTGCCGAAG	84182
rs564235425	snp	A/G	0	0	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30813431	TACAGCCTTTCCACC[A/G]TTGAGTGGCTGGATT	84182
rs564250529	in-del	-/CTC	0.00993419	0.0697739	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30866953	TCCCATCCTAGCCCT[-/CTC]CTCTTACTGCTTTGA	84182
rs564255454	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30827238	GCTTAGTACCAATGC[C/T]TTAGTCCTTGATTTT	84182
rs564280510	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30783262	GGACATCACTCTAGC[C/T]TCTGCTTGTGTTGTT	84182
rs564286356	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30792986	TTTTGTCTGTATTCC[A/G]TAAGTTAATACGTTA	84182
rs564356568	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30790417	TTTACCACAGGATTT[A/T]AAAAAACCTTTCATT	84182
rs564374516	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30874003	TGGGGCAGGGGTATT[A/G]GTGTTAACTGAGGGA	84182
rs564402078	in-del	-/T	0.00478085	0.0486577	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30820336	TTCCCTTTTGCCACA[-/T]TTTTTCTTTATATAA	84182
rs564403479	snp	A/G	0.00358779	0.0422022	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30788793	GCTGCCATCCTCCAC[A/G]GTCAGCGGAATGCCT	84182
rs564439820	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30873447	GTGTGTCAGTTTCCT[C/T]ATTTGTACAAGAGGC	84182
rs564450037	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30879392	CAGACCTCCAGCTTC[C/T]GGAACTCTGAGATAA	84182
rs564497276	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30884048	GATTTGGTGTGATCT[A/C]AGAGAATCTCCATTT	84182
rs564508518	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778404	TTGATTTAAGATGGT[A/C]AACAGCGATTCAGCT	84182
rs564561740	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30887622	AGTGCCTGGGAGGGC[A/G]GGGCCACTCCCTAAG	84182
rs564562582	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30862371	CTGCATGTGGGAGTG[C/T]GCCCGTGAATAAGCC	84182
rs564572193	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30862522	TACCAGGCTCTGCTG[A/G]AGGTTTGCGGTGATT	84182
rs564602234	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30829281	CTTTAGTTTTGAAGC[A/G]AACTTTTTTTCTCTC	84182
rs564627846	snp	A/C	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30868490	TTGTGCAGCCTGCTC[A/C]GTGGCAGAGCCTCTT	84182
rs564632929	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30787440	GTAAGAGATTTCTTC[A/G]AATATGGAGGTTGGA	84182
rs564666632	snp	A/G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828850	CCACCTGACCTCAGC[A/G/T]AGTGGGGCTGGTCAA	84182
rs564668475	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778627	CTCATGGGCCCTGCC[A/G]GTGACAGGAGAGGCT	84182
rs564676831	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30834513	GTGATGGGAGGGCGT[A/G]CCATGAAGACCTCTG	84182
rs564737540	snp	C/T	0.00676609	0.0577691	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30780996	GAGTTTGGTTGTAGT[C/T]CATGGGCTGTGGGTC	84182
rs564757594	snp	C/T	0	0	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30792997	TTCCGTAAGTTAATA[C/T]GTTACATATTCGTAT	84182
rs564771474	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839528	CCTCTGCTTTGGAGA[A/T]GTTAAAATTGAACAT	84182
rs564796220	snp	G/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30796621	AATCCAAACCCTTTA[G/T]TTGGCAGGCGGGGAA	84182
rs564814891	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875909	TCGAGGGATTTCTGC[C/T]GTGATTGTGGGTCAC	84182
rs564819804	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30864703	GGTATCCCCAAAAGG[C/T]AGTCACTGCCCAGAG	84182
rs564825444	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30867798	TGGTGCCCTAGTGGT[C/T]AGGTGGAGGGGGGAT	84182
rs564838856	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30825874	AATTTATTATCTCAT[A/G]GTTCTGGAGGGCTGA	84182
rs564874282	snp	A/C	8.30186e-05	0.00644223	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882249	GAGCCACTTCAGCAT[A/C]CTCTTTAGCCTGCAG	84182
rs564932451	snp	A/C	0.00795532	0.062565	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30833370	GAGAGCCTGTGTAGG[A/C]AAGCTTCTGTTTTTA	84182
rs565009854	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30837981	ATGAAAAGGAAAAAA[A/G]GAGCTGATTCTGGTG	84182
rs565078328	in-del	-/T	0.00358779	0.0422022	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30841629	TTCTGGCAATTGGCC[-/T]TTTTTTAAAAAAAAA	84182
rs565098698	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828532	CCTGTGGCTGAGAGA[A/G]GGGGAGTATTCAAGG	84182
rs565149158	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30841456	AGAGGCAGATAGAAA[A/C]CCCCAATCCCATACC	84182
rs565221811	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30812767	CCTTTTCCAGACCAG[C/T]CTTACCCCCTCTAAC	84182
rs565242909	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30800873	GTTTTTCAGGTTTTG[C/T]AGAAGAATGGACAGT	84182
rs565282240	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30812276	ATGTGTGTTGAGGGG[A/G]GGGGGGTATGTATGT	84182
rs565290292	in-del	-/A			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30807505	ATCCATTTTAGATTT[-/A]AAAAAAAAAGCCGGT	84182
rs565290404	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30793681	CCATCGTGGGCCCAG[A/G]GCAGGTATTCTCATA	84182
rs565297946	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30788343	CAGTTTCGCTTGATA[G/T]GTCTTGCACTTTGAA	84182
rs565299445	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30794883	GTGCTGTGTTGCGGG[C/T]GGGGGCCTTTCTCTA	84182
rs565303096	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30861960	GAGGAGGGACCATGG[A/G]ACCAAGCCCCGCCCA	84182
rs565310591	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30883408	CCAGCCTGGGGGTGG[C/T]AGGAGGTGCTGCCTG	84182
rs565335877	in-del	-/ATG	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30851432	AGAAATGATATAAAT[-/ATG]ATTATCAGTTTAAAT	84182
rs565353579	in-del	-/A	0.00318978	0.0398085	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30855282	TCAAAGAAGAACCTT[-/A]AACACTTGGAGAAGG	84182
rs565373133	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30801296	ATGCATTATTTGGAC[C/T]TCACATCAGACTATT	84182
rs565375473	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30871995	AGGCAGAGCCCTGGT[A/G]CGGCTGGAGTGGAGG	84182
rs565377375	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30877784	TCAAGCAATTCTTCT[C/G]CCTCAGCCTCCTGAG	84182
rs565379969	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30848659	GGGCCAGTGCTCCCA[A/G]CAGCTGGGGCATCCG	84182
rs565409817	snp	A/G	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30834734	AACAGCACTCAAGTC[A/G]CCTCTTGAATGCTTT	84182
rs565416958	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30887642	CACTCCCTAAGCAGG[C/T]GTCCAGGAGGAACAG	84182
rs565431406	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30781664	AGTTATTCCTTGGAG[A/C]AAAAAATGAAGAGGA	84182
rs565453086	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30885451	TGGGAGGCGAAGATT[G/T]CAGTGAGCTGAGATC	84182
rs565489197	snp	C/T	3.31824e-05	0.00407309	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852321	CAAACTTTGGCTTTG[C/T]TTGGGGACTGTCTCC	84182
rs565568041	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30888424	AAATGCCTTAGGTAC[C/T]GAGGATGAGAGACCC	84182
rs565572930	snp	C/T	0.00358779	0.0422022	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30881897	ATGCAGAATGAGCAG[C/T]ACTGGGAACCATTAG	84182
rs565595888	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853254	GCCTCTCAGCCCTGA[C/G]TTGGAGATGCTGCTC	84182
rs565598333	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30888688	CACTAGCACAACATG[C/T]GTCATGGCTCAGCCC	84182
rs565616797	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30819220	ACTTTAACTGCTTCC[C/T]GTAAGACTTTATAAG	84182
rs565653585	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30843757	GGTTTTCTATCTGTC[A/G]TTGCCGGCCAGGCAG	84182
rs565682875	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828983	ACTGTGGGGCCAGAG[A/C]AGCTCTTTCTGCTTT	84182
rs565684912	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771961	CCCACTCGGAAAGAA[C/T]TTCTCCCAGAGGGAA	84182
rs565704672	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30802752	TTCATACAAAACTAG[G/T]TACATGACTGCCTGA	84182
rs565745732	snp	G/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30867927	CCCTAGAGATTTCTT[G/T]CTCCAGTCCTCTGGC	84182
rs565765554	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30861187	AGCCCTGCTATGGTG[C/T]TCGGGCCAGGCAGGC	84182
rs565785534	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30796789	TTCACTTAAAGCCTC[C/T]ATCACAGATGTCACT	84182
rs565824340	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30789917	CTCTAGAATTCCTTC[A/G]TTTCAAAAACTAAGC	84182
rs565848055	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30796225	GTTTTTCACATTTCC[C/G]CCTGTCTCACTGTCA	84182
rs565884968	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30880509	CACTTTTGTCTCTCC[A/G]TTGGAAAATTCAGGG	84182
rs565896022	snp	A/G	0	0	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30885439	ATCGCTTGAACCTGG[A/G]AGGCGAAGATTGCAG	84182
rs565896188	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30878828	CCCATTTACTCAACC[A/G]GGAGCACGTCCTCTC	84182
rs565904845	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30798055	GAAGTGGAAACATCA[C/T]AGAGTGTACTTACAC	84182
rs565945200	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30802331	TGCATTAACCTGAGA[A/G]GGAAGGTCTCTTAAA	84182
rs565969769	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30844040	ATGGTGTAGGAGAGT[A/G]ACCTCGCTTTTGTTT	84182
rs566024728	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30856503	TGTAATAATAGTTCC[C/T]CAAATTTACACAGAG	84182
rs566028242	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30884789	GACTTCTTGGGCTCA[C/G]CTCTAATTGACAATT	84182
rs566029052	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771829	GCTCCGGGGCGGCGG[C/T]AGCTGGGGAGGGGGC	84182
rs566037206	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30862463	ACTGCACTCCAGCGG[C/T]GCTCCCTGCATCCCG	84182
rs566057142	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30851781	CTCCGATTCCTGGAC[A/G]TCTTGGGCTACACAC	84182
rs566062768	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30835712	ACTCTGGCAGGCCCC[C/T]CTAGGGAGCTGGATT	84182
rs566090005	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30886942	ACCTCTCTCATGCTT[C/G]CAGCCTGGCTAGAGT	84182
rs566113016	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30794123	ACATACTACACAACT[C/G]TACACAGTGCTCTTG	84182
rs566125966	snp	A/C	1.67027e-05	0.00288982	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840852	CGACTGTGCTCAGTA[A/C]GTCAGTGCTCTTTCT	84182
rs566158884	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30826196	AGAATCTCTTTTGCC[A/G]TGTAAAGTAACATTC	84182
rs566180972	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30845839	GGACTGTCTGGCTTC[A/G]TTACGACTCATTCCA	84182
rs566209335	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30803614	TGGCAGGGGGCAGTC[C/T]TATTCTTCAGGCCTT	84182
rs566210360	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30800573	TTGGGTGCTAAATTG[C/T]GGCCCTCACAAAGGA	84182
rs566212516	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30769878	GTGGCTATTACTGCT[C/T]GGGAACACTTTCCTT	84182
rs566225780	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30886417	ACCCAGCTCTGTTGC[C/G]CTGCAAGAACCCCCA	84182
rs566236055	snp	A/G	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30809811	GGGAAAAAAAAGGGG[A/G]GCAGAATTTATGTAA	84182
rs566263790	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30892087	CCCCAAGCCTCTGGG[A/G]CAGGTCTCATGTACC	84182
rs566280052	snp	A/T	0.0189856	0.0955633	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30822627	TGACGTGCCTGTCTA[A/T]TTTATTTATTTATTT	84182
rs566294331	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30877415	TCAGGCCCTACAACC[A/G]TCTCCCCTCCTCGTG	84182
rs566341397	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30775176	ACTACCAAGAGTTAG[C/T]GCAGACCCTGCAGGT	84182
rs566377910	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30871701	TTGAGCAAGACATCC[C/T]TTTTCTGAGGCTTGG	84182
rs566440520	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30818102	AAATAAAACCCTTTC[C/T]TTCCCTTGAGCATGC	84182
rs566460847	snp	C/T	0.00398564	0.0444627	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30838159	CATGAGGGGAGTGGG[C/T]GGGGACCTGCTGCCT	84182
rs566465662	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30818118	TTCCCTTGAGCATGC[C/T]AAGAATTATTTTTAA	84182
rs566476872	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836823	ATGGATATAGATGGC[A/G]TGATTTTGGTGTTTC	84182
rs566476935	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30876974	ATGTTGGGGTGTGCT[A/G]TGTCTTGCTAATGAC	84182
rs566480432	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30784358	CCCAGAGTGATAGTA[A/G]GCACTTTCCTTCTTT	84182
rs566487863	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30814267	AGCTTCATTAGCTTC[A/C]TGGTAAATCAAATGC	84182
rs566488942	snp	C/G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30806716	AATGAATTTGCCTGC[C/G/T]TTGAGGCATTTCCTT	84182
rs566502573	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30812569	GGTATAAAACCCAAG[G/T]CTAGCCCAAAACACG	84182
rs566514898	snp	G/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30848797	TTGTTGCTTGTCTCA[G/T]TGGATTTGAAGGATT	84182
rs566520144	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30837478	GCATACAAATCAAAG[A/G]GCAAAATATTTTTCT	84182
rs566543489	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30807338	AACCCATCCACACAC[A/G]GAATTCTCACACCCA	84182
rs566549292	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30821084	CAAAAAAATGTGAGA[C/T]TTTAAGAAGCTTTAA	84182
rs566549901	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30848151	CCTTACTTCCAGATA[A/T]GGAGTTTTTCCAGCT	84182
rs566602860	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30812908	GCCCAGAATGGGTCC[A/G]GCTGCTTCCGATGGT	84182
rs566609759	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30889504	ATGGGCACTCACTGC[C/T]GAGGAGAAGTCTGAC	84182
rs566672411	in-del	-/CTTTTGTTTACATTTTTT	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778109	GGAATGAATATTAGC[-/CTTTTGTTTACATTTTTT]CTTTTGTTTACATTT	84182
rs566688845	snp	C/T	0.0023933	0.0345097	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30818636	GTTCCAGAGTCCGAG[C/T]GTACTCTATTTGGGA	84182
rs566712089	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30807930	CTGAAGCTCCCGGCC[A/G]AATAAAGCCCTTCCT	84182
rs566721142	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30819925	TTTTTTTTTTGAGAC[A/G]GAGTCTCGCTCTGTC	84182
rs566753051	snp	C/T	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30890235	GAAGGTACAATTCAG[C/T]GTTCCTATTTGGACA	84182
rs566759333	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30777160	GACTGCAGGCCTATG[A/G]CACCATGCCCAGGCC	84182
rs566793999	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30787670	AGCCTTCCATTAGTC[A/G]GAGCCACCTCAGCAG	84182
rs566801474	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30817931	GGACTCTGGTCCTGG[A/G]GTTTTCAGTTTCACT	84182
rs566834494	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30877301	TCTTGGGTCGAGGGC[A/G]TTGGTCAGAGAGTAA	84182
rs566840671	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771123	TTAGTCCTCCAGAAA[C/T]AAGGAGGCAGGTATT	84182
rs566845466	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30854716	TGTCAGACTGCCTTC[C/T]GCAGAACTTTCCCAA	84182
rs566877889	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30816924	AGGTCAACCGTTTGA[A/G]AACTGGCAACTGCAG	84182
rs566883544	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30770626	TTGTTTAAGCCACAT[C/G]GTCTGTGGTACTTTG	84182
rs566918406	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30879739	GTCCTTCTCATTGTC[C/T]CCTCCATACCTTGTC	84182
rs566966654	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30776608	AGCAACTGGACTTAC[A/G]GACTAGTGGTCTGTT	84182
rs566970031	snp	A/C/T	0.000563317	0.0167736	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782183	AGATGCAGGATGGAG[A/C/T]ACATCATTGTCAGAA	84182
rs566981293	in-del	-/AG	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778933	TGCCCTGCTTATGTA[-/AG]AGTTTCCTTCTTCAG	84182
rs566986694	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782999	GCTAGATTGATACTT[A/G]ACTAAACAATTGGGT	84182
rs567019113	snp	C/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30866761	CAGAGGGTCTAGTTG[C/G]GAGGGAAGGAGCTGG	84182
rs567049535	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30823593	ACTCTTCAAAACTGC[C/G]CATTCTTTTTTCATA	84182
rs567066357	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30833637	CCAAAGTCTTAACTC[A/C]TTTCAGCATTAACCT	84182
rs567095365	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30826524	TGAGCTGAGACGTTC[A/G]GCTTGGAGGAAATGC	84182
rs567206984	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30810593	TTAAAGTAAAAACAC[A/G]ACCGGTTTTTCTTAA	84182
rs567219255	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859631	ACTCAGGGGGATGCC[C/T]CTGGCACTTGTGCAG	84182
rs567220124	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30797297	CAGCCCACAATAACA[C/G]CAAAACAAGGAAATA	84182
rs567226192	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30797544	TGGGAGCATGTTACT[A/G]ATTGAGGCTGGACTA	84182
rs567259662	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30887190	CTGACCATTTTGCCC[A/T]GGCTCCCTGTCCACA	84182
rs567278264	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	FAM188B, INMT-FAM188B	GRCh38.p7	7:30892813	GTAGTCTGAGCCTTG[C/T]TTGTTCCATTCATTG	84182
rs567284847	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785431	TGACTGTACTGAAAG[G/T]TTATAGTTTTCCTTA	84182
rs567286404	snp	G/T			utr-variant-3-prime, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30892078	ACAGCTGAACCCCAA[G/T]CCTCTGGGGCAGGTC	84182
rs567339695	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30830310	AGAGGTATCTTCCCA[C/T]AGCAACACATGAAGC	84182
rs567342466	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30857284	GCTTTCTCCAAAAAC[C/T]CTTCCTTGATACTCC	84182
rs567369251	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30779257	AGAAGCCAGAAATGC[A/T]GTCTTTTTTGTTCAC	84182
rs567371286	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30863123	CAGATGATCGCCGAG[A/G]GCCTTCCTGTTCTGG	84182
rs567406208	snp	C/T	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778670	GGCCTGTCACACTTG[C/T]GGTCAGAGAGAAACG	84182
rs567427634	snp	A/G	0.00517822	0.0506191	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30842384	CATCAGCTCTCCCTG[A/G]TGGGCTCAACACAGT	84182
rs567436806	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30869457	GGGCTGCCATAATGA[C/T]AGACATTCGTGTCTT	84182
rs567476613	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30784834	CCACAATCACAGCAC[A/G]CACGACTGCCCCTCC	84182
rs567511903	in-del	-/A	0.287346	0.247195	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30845519	GACATGATCCAGCTT[-/A]AAAAAAAAAAAAAAA	84182
rs567560291	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30805066	AGTTCTCTTGTGTTT[A/T]GGGTTCTGTTGTTTT	84182
rs567563826	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30831700	ATATCTTGTGGTCAG[C/T]AGGAAATTCTGCACA	84182
rs567570514	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30841161	TTCCACCCACCAGGT[C/T]GACCTGCCGACCTTT	84182
rs567572629	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30846943	CTTCACTGGCTCGTC[C/T]GCTGCTCACCTCCTG	84182
rs567577947	in-del	-/ACCTG			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782618	TGAGGCTGGAAGATC[-/ACCTG]AGCCCAGGAGTTCAA	84182
rs567662217	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30825223	CTGACCTTTTAAACT[C/T]TGTAAAGCTTATGCC	84182
rs567710671	snp	C/G	3.31219e-05	0.00406938	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785957	GGTCTGATTGTGCGA[C/G]GCATGATGTCTGGGC	84182
rs567720931	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30793364	TTTAGTATTTTTTTT[A/T]AGCAGGTATGTTAAA	84182
rs567724621	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30784253	TTGAAGCTCCTGAGT[A/C]CCACCCAGTTACCCA	84182
rs567842936	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30805162	AGCAGGGCCCCTGCC[A/G]GGAAGGCAAGTGGGC	84182
rs567852958	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30803768	AGCTCTCTTGTTCTT[C/T]CCCAGCGTGTTTTTC	84182
rs567857264	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30873645	AGGGACTGCTAAGCT[C/T]TGCCATTGTGTGACT	84182
rs567858410	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872765	GGGCCCTCAATGGAC[C/T]TCACAGGGGCAAAGA	84182
rs567873955	snp	G/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30881828	ACTGCCGTGGTGCAG[G/T]TTGGAGGCTGAGTAG	84182
rs567900644	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30844185	AGTGAAGCGGTCTGA[C/T]TTCCTGCTCCCACAG	84182
rs567907669	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30811158	CTGTTCATTCAGCGG[A/G]AAAGGGATGGACTCA	84182
rs567962395	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30843748	GAGGAGTGAGGTTTT[A/C]TATCTGTCGTTGCCG	84182
rs567976424	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30849547	GGTCTCTGCCATGTT[G/T]GATACAGCTGACTGC	84182
rs568026471	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30833951	GGTCTTGGGCAGCTC[C/T]GCCCCTGTGGCTTTG	84182
rs568026894	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30833805	GGGAGAAATTGGCCA[A/G]AACAAAGGGGCCCAG	84182
rs568049778	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30834184	CCCTAGCAGAGGTTC[C/T]CCATGAGGGCCCCGC	84182
rs568071874	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30789827	CCCACCCTCCCATTA[A/G]TAACAACATGAGTTC	84182
rs568107388	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30868700	GTTTCTTGATACAGC[A/G]TAGTATCTCAGGGAC	84182
rs568115970	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30878129	AGGGCCCTTGCTCTG[C/G]CCTGGCCTGGCCCTC	84182
rs568122154	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30786989	TCTGTGTCCACCTGC[A/G]CTCTCACTTACCTGC	84182
rs568125382	snp	A/G	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30873107	TGGAAACCTACGTGG[A/G]CACCATACAAGGCAA	84182
rs568130761	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30886299	GAAGAAACAGCTGAG[C/T]AAGACTTGGCTCCTG	84182
rs568149847	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30796048	GGGTCTGGGATTAGG[A/G]TGTGGACATAGTTGA	84182
rs568195153	snp	A/C	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30802936	CATCTCACCCACCCA[A/C]CCAACCAACCCACCC	84182
rs568216614	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30884637	CCTCCGTCTGACTCT[G/T]TGTCTCTCTACCCCT	84182
rs568226739	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30801761	TTCCAAGTCTCTGAT[A/C]TGATGCGTCTGCAGA	84182
rs568243595	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30885713	CAGTGCCCACCCCCC[C/G]CCCAACCCTGCTGCC	84182
rs568261989	snp	C/T	1.65622e-05	0.00287764	utr-variant-3-prime, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30892014	CCTGTGACCGTTGGA[C/T]GTGGGTAAACCCTGT	84182
rs568278047	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30884272	GGAGCGCCGAGACAT[C/T]CTCGACATGCTTTGT	84182
rs568286719	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771745	CCACGAGGCGTTTCT[A/G]CCGTCGTCACCGGGC	84182
rs568293585	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30770008	TGTTGGGCCGGGTGC[A/G]GTGGCTCACGCCTGT	84182
rs568301220	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30891580	TATCTAGGACTGCAC[A/G]GGTGCCTCTAAAGTG	84182
rs568326520	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778013	GTTTGGGATGGTTAC[A/G]GCCCCCACCTGTGAT	84182
rs568326719	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782300	GTTTCAGTCAGTATT[C/T]TCCAGAGGAACAGAA	84182
rs568337695	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30807900	GGAGCTCGGTTGTTG[A/G]AGATGTGAGTCTTGC	84182
rs568393577	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30817512	CTGTTGAAGTGATGG[C/G]GGTTATACAGAGTCA	84182
rs568397844	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30880470	CCCTTAATCTCTCGA[C/T]TGTTACTTCTGCATG	84182
rs568403340	snp	C/T	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30807665	CCTGGTAGTTAAAGA[C/T]TGACCCCTGACCTAA	84182
rs568411824	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30777406	CACCTCTCCTTCAAA[C/T]GGACTCTTCCCGATG	84182
rs568415998	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30861258	TCCCCTCTCCTAAGA[C/T]GACAGTGTGTAGGCA	84182
rs568424427	snp	G/T	0.0023933	0.0345097	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850846	GGTGACCCCTCAGAG[G/T]AAGCCTCTGACCCCT	84182
rs568453169	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30856718	TTGTGACTGTCCAAG[C/G]GGAGATGGAAATTTG	84182
rs568467530	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30838262	GATGGGAAATGAACA[A/G]TGAACTCATTATCAG	84182
rs568496954	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30879103	AGACTGTTGTGAGCT[A/G]AACTATGTCTCCCCA	84182
rs568517490	snp	C/T	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30845341	GGAAACACTGGGTCA[C/T]GTGGGCAGGAACCTC	84182
rs568518878	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30888742	CTTTGATTTTCTATT[A/G]TAATTGCAAACTGCT	84182
rs568570802	snp	C/T	0.0103295	0.0711199	upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771356	GCCCCAGCCCGCCAG[C/T]CCCAGGGAAGGGGAG	84182
rs568595013	snp	A/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30815078	TGGTTGGTCTTTATA[A/T]GGACAGTCATGGGCA	84182
rs568656900	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30888277	AGCGAGTGGTCTCAA[C/T]GGGACAATTGTGTGC	84182
rs568669339	snp	C/T	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30845665	TTTCCTGCCTGTGTG[C/T]GGGGTCTGCCTTGGC	84182
rs568683162	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30821919	GAGTACAATGAATAT[C/G]TGTAGACTTTTCACT	84182
rs568733148	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30784750	TTCCCCAGGCTGGTT[C/T]CAGCCTCTTCTCTGC	84182
rs568737745	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30842265	TGCTCTCCGGTCGAT[C/G]CTTCGTGGCTCTTGT	84182
rs568764076	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30779808	AATCCTTTTTTCAAA[C/T]GAGACTTCAGCAGAT	84182
rs568795319	snp	G/T	0.0023933	0.0345097	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30821427	TTGAAGATGTTATTT[G/T]ATTGTCTTATGCCCT	84182
rs568841147	snp	C/T	0.00557542	0.0525036	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30810132	GGCGAGCCGAGATTG[C/T]GCCACACACTCCAGC	84182
rs568852742	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882537	CCTCCCTGCAGGAGG[C/T]GGCCAGAGCTGGGCC	84182
rs568875057	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30841832	TATATTAATAATTAA[A/G]TGGATTTTAAAACCA	84182
rs568900216	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30811810	TCAATCGATCACGAC[C/T]CTCTCATGCGGACTC	84182
rs568919862	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30848213	CACGATTTTGTGTAA[C/T]GTCTATCCATGTTGG	84182
rs568934142	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853341	AAGCTAATTCAGGAT[A/G]GGGCACTGCGTGGGG	84182
rs568978589	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30806852	CAGGCCTGGACAATG[A/G]GCTGGCACAATTGGC	84182
rs568995903	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852976	TCCTAAGGGCTGCTT[C/T]CTGCTGAACTCAGGA	84182
rs569020539	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30833692	TTTGAGACAAGGCAA[A/G]TCCCTTCCACCTATT	84182
rs569042471	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30819618	TGAAGAGTTTCTCCT[C/T]GTAGTTCTGTCAAAT	84182
rs569048044	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30774190	CTCTCTTCAAACCCT[C/G]AAGCTCCTTCCCCAT	84182
rs569081974	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30856352	CAAAATGGAATATTG[A/G]TGCCATTTAGTGTGT	84182
rs569090259	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30825135	TGAAAAAGTGTTTTG[A/G]GTCCCTTGATTTATC	84182
rs569144014	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30863885	TTGCCAAGCTTTGCT[G/T]CTTTTCAAACCACAT	84182
rs569177100	snp	A/G	0.00517822	0.0506191	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30819692	TTTCATGATGGCTAC[A/G]TTTTTCTGTTGAATT	84182
rs569203517	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30831554	CAGAGGCTGGACCGG[C/G]ATGGTGGGTGAGAGA	84182
rs569209497	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30800402	AGCCCTCTGCAAGAG[C/T]ATCATATTACCCATT	84182
rs569248919	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30876225	TGATGCTTCTGTAGA[C/T]GTATCACTCCAGTCT	84182
rs569249050	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30860129	TACTTTGAGGGATGC[A/G]GGTGGGGTAGGACTT	84182
rs569267618	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30874171	GTGTCACAGGCAGCG[C/T]CAGCTGTGGCAGAAG	84182
rs569269883	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30860501	TCCCCAGGACTGGGT[C/T]TGCTCCTGGTTTGGC	84182
rs569366374	in-del	-/TT	0.0142736	0.0832652	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828316	ATGACAAGAACTCGA[-/TT]TTTGTGTGTGTGTGT	84182
rs569383077	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30865834	CTCCTGGCTCTCAAT[C/T]GAAGACCCTGTGCCT	84182
rs569390881	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30858761	GCTGCTCTTAGCACA[A/G]CACAGTTCTTCTGAG	84182
rs569439572	snp	A/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30865136	CCAGGAGCCTGACCC[A/T]TGGGCTCCCGTCTCT	84182
rs569442364	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30829642	TGCGGAGGTGGAGGT[A/G]GGGGTTTGTTTACTC	84182
rs569492563	snp	G/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30876821	ATTCACCACCTATCC[G/T]CAGAACCAGGACGCA	84182
rs569501074	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30815061	TTACTTCCCTGACAC[A/G]TTGGTTGGTCTTTAT	84182
rs569506177	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30829074	AAACAGTTCTCATTC[A/G]AAGTATCAGTATAGC	84182
rs569507374	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30789868	TACTCATCTTTGACG[A/G]TAAGGGAGGATATTT	84182
rs569546389	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30823531	TCAATATTTAATGTA[G/T]CATCTATCACCATTG	84182
rs569550830	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30871605	AGGTTTTCACCTTGC[A/G]TCTTTTGAAGGACTC	84182
rs569579560	snp	C/G/T	1.65616e-05	0.00287759	utr-variant-3-prime, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30892007	ACCCCATCCTGTGAC[C/G/T]GTTGGATGTGGGTAA	84182
rs569586680	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30815684	TTTTCCTTCGAGAAG[A/G]TATTTTTCTCTCCCT	84182
rs569596627	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30817005	CACGCGATGACTTCT[C/T]GATAACCCAACCCTT	84182
rs569649583	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30822760	CCACCTGAAGCCTCC[C/T]GAGCAGCTAGGACTA	84182
rs569669933	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30856756	TTAGGTAGGCTTTCT[A/G]TGGAAAGGGACACCG	84182
rs569720834	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30784775	CTCTGCCTGACATGC[C/T]GCAATCACAAGGCTG	84182
rs569723637	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30797493	CTTTGATCTCTGGAC[A/G]CAAATGCCGACAGCA	84182
rs569756374	snp	C/T	0.00358779	0.0422022	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840347	GGGCTCACTGCCAGC[C/T]GAGATGGTCAGGAAA	84182
rs569774069	snp	A/C	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30868934	TCAGGGCAGCCAGGG[A/C]AGCCAGGGCCAAGCC	84182
rs569833922	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30880442	ATTTATAAAGTCTGT[A/G]GGCAGCTTTTTTCCC	84182
rs569837466	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30874215	AGAGACCTGCCTGCC[A/C]TAGTGCTGGGGCTGG	84182
rs569837558	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30867959	TTCTAAGTGAAGACA[C/T]AAGCTGAGAGAGAGG	84182
rs569845768	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30858874	TGAGCCTCAGTTCCA[C/T]ATATGCTAGAGGGCA	84182
rs569860974	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30874830	TAGTTATTGGTACTG[C/T]ACCATGGTCAGTTTC	84182
rs569942172	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30860909	CACAGCCTCATGCTT[A/G]TGGGCCTGAAGTCAC	84182
rs569960847	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30846314	AGGCTATTTTGAGAA[A/G]GTTAGGGTAGAAACA	84182
rs569972555	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30851835	GGAGCCTCGGAGAGG[A/T]TGGAGGTGGAGTTCC	84182
rs569975039	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30841006	GCTGACAAGGCCTGC[A/G]CAGACCAGTGTTAAG	84182
rs569979671	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30879711	TGCCCTCATAACCCC[A/G]TCTAAGTAGGGGGTC	84182
rs570019891	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30841101	GGCTGCAGGAACGAC[A/G]TCAAAACCAATTTCC	84182
rs570036065	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30842163	TTTCCTCTCCAACCA[A/G]AAATGCTAATCAGAA	84182
rs570036923	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30851078	GCATCGTCTCTTCAC[C/T]GCTGGCCCCATTCTA	84182
rs570050420	in-del	-/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30808971	GGCAGAGAGAGAGAA[-/G]AGAGACAAATGGGAA	84182
rs570097105	snp	C/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791673	GGAACTTCTTAGTCT[C/G]CTTGGTCTCTCAGAA	84182
rs570098789	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30794277	GGTCTCAGTCCTAGT[A/G]TGTACCAGGTCCTGT	84182
rs570189251	snp	C/T	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30881184	GGTCAGGAGAGGCGC[C/T]GGCCAAGAAGTGTCA	84182
rs570207026	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30824433	ATTAAATTTCAACAT[G/T]AGTTTTAGAGGGGTC	84182
rs570209715	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840923	GAAAAAACAAGCAAG[A/G]AAGCATGTGTGTTCC	84182
rs570220240	in-del	-/AAAC	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30885517	AACTCCGTCTCAAAA[-/AAAC]AAACAAACAAAAAAC	84182
rs570225118	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30804532	CGACAAATATGTACT[A/C]CAGGATTAAGAAAAA	84182
rs570250316	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30887151	ACCCCCACTCCCTGC[A/G]GAACCTCCCGTTCAG	84182
rs570254643	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30774669	GAATTTTTAGTCCTC[A/G]CCCTTCTTGATCTAA	84182
rs570271401	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30889129	ACCCTCTGGGAGTCT[A/G]GATTCAGGATGTGTT	84182
rs570287040	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30777083	GGTGTAATCATAGCT[C/T]ACTGTGGCCTTGAAG	84182
rs570417044	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30794566	AGGCGGTGTGAGTAT[C/G]TGTGCAGTCAGGCCC	84182
rs570474433	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30809196	ACAAGGGTGTATCCC[A/G]AAAGCACTGAGGCCT	84182
rs570483166	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30843620	GGCCACATCCATGGG[A/G]TGGAAGCCCACTGCT	84182
rs570500404	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30801066	CTAGAGCCTCTGGAG[A/G]CCCCCAGATCTGGAG	84182
rs570501251	snp	C/T	3.31214e-05	0.00406935	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875444	CTCCTCTCCACTCTT[C/T]CAGTAACTGATTCAG	84182
rs570503368	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30814586	AATTAAATTTTAAAA[C/T]GTGCTTAGCAAGTGC	84182
rs570506138	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30838513	TGCTGGCAGTGTGAT[C/T]TCTGCTGCACCTATT	84182
rs570515643	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782411	CTGTATGTATACATA[A/G]AGAAGTTTGGCCAGG	84182
rs570530586	snp	A/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30838211	ATGGGGAAGGGATTG[A/T]CCATTCTGGGGGCTC	84182
rs570558449	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30889596	AAGATGAACGCTCTG[A/G]TATGGATAAATTCCA	84182
rs570573899	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30884178	GTTGATGCCCACCAC[A/G]GGAAAGCGAGCCCTT	84182
rs570600352	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30848893	GGCCCAAGTGGGGAC[C/T]TAATGGTTTCATAAA	84182
rs570605296	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30789585	AAGTTTGAGTCTCCT[C/T]GGGAATGGTGACTAA	84182
rs570605729	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30807879	GGACAGGAATTGCTC[A/G]CTCGGGGAGCTCGGT	84182
rs570727600	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30783580	AAAATTACAACCTCT[C/G]GCATAAATGAATTAA	84182
rs570753491	snp	C/T	3.31307e-05	0.00406992	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782060	TACGGCTAACAATTT[C/T]ACTCAAGATACCCCA	84182
rs570760080	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30819599	TTCTATTATGCTCAC[A/G]GATTGAAGAGTTTCT	84182
rs570771537	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30857052	AATGAAGACGAGGTT[A/G]ATTTAACATTGTTGT	84182
rs570771874	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30881349	CCACAAACACTTCCA[C/G]CATGTGAAATTCCCC	84182
rs570776363	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30884911	TTCCTCTTCTATTGG[C/T]TGCCTTCATCTCCCA	84182
rs570796362	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30812617	GAATTTCTTGTTACA[C/T]GGGCATCCGCAAGCT	84182
rs570850416	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30789112	TATGAAAATAGTTTT[A/G]AATTCCCTAAAAGGA	84182
rs570902137	snp	A/G	0.000399281	0.0141238	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850509	GTCCTGGCCCTCGCA[A/G]ACATTGTGTGGCGGG	84182
rs570927798	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30841779	GTACTCCAGAAGCAT[C/T]CTCTGGTACCCAGCA	84182
rs570930843	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30817778	TAGCATGTGCGTGTC[C/T]ATCCACTTCCTATAT	84182
rs570974685	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30776675	TGAGCATGTGGATGA[C/T]GCTGAACAAATAGCT	84182
rs571070975	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30866923	TTCCACCAACTCTCC[C/T]CCTGCCTCCTGGGCT	84182
rs571120331	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30888259	ACCATGGTGTTTTTA[C/T]GGAGCGAGTGGTCTC	84182
rs571123606	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30867419	AAAGGAAGTGACATT[C/T]ACCGAATGCCAAATG	84182
rs571129644	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30834120	CTAGGTGGTGCCCCC[C/G]TAGGGATTCTTTGTG	84182
rs571157506	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30870227	CCCGCTGGGTGAACA[C/T]GAGGTAATGATCTTA	84182
rs571163674	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785500	TTAAGGACTTGAGGG[A/G]TCCTGTTATGGATCA	84182
rs571190515	in-del	-/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30885796	ACTGGGCCAGGGGAA[-/C]CTTCTTCCTGGCTCC	84182
rs571194133	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30846398	CCCTCAAGATCATTT[A/T]TTTTCCCTATCTCTA	84182
rs571218397	snp	C/T	6.62383e-05	0.00575454	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875545	GTCCAACGTTTTCAA[C/T]GATGTGGTTGAGCTG	84182
rs571250988	snp	A/G	1.77106e-05	0.00297573	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791574	AGCCCGCACCTGTCA[A/G]GTGAGTGTGCTATGC	84182
rs571256313	in-del	-/GACCGGTG			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30789164	GTGGACTACTCTGAG[-/GACCGGTG]AACCAGAGAGGAGCG	84182
rs571320489	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30863855	TTCCGGTAAATCTCA[A/T]GCAGGATTTCATGCT	84182
rs571351337	in-del	-/TGGGGGG	0.498503	0.0273153	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30824981	GCTCATGCCTCTCTC[-/TGGGGGG]TGGGGGGCATGAGAG	84182
rs571352877	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30824341	TTTATGATCCCATTA[A/T]TCCATTCATGAGGGC	84182
rs571356917	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852455	TGGCTTTGGGGATGG[C/G]CTCCTGCTAGAGCTG	84182
rs571362108	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30830746	GGACACAGCCAAACC[A/G]TATCAGTTCTGGAAG	84182
rs571402129	in-del	-/TTTTAA	0.00795532	0.062565	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30833366	AGAGAGAGCCTGTGT[-/TTTTAA]AGGCAAGCTTCTGTT	84182
rs571425418	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30823691	CAGCCTCTCTGAGAT[G/T]TTTGCTCCATCTTGA	84182
rs571437296	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30779302	ACATAAAGTGTTGTC[C/T]GATGGCATAGTGAAA	84182
rs571492072	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30837178	TAACAATTCTTCAGC[A/G]CTGTTCAGGTGTACT	84182
rs571492125	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30831753	GGCCCATTCTCCCTA[G/T]GGAATCTTCCTATGA	84182
rs571515028	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30863237	CTGGTAGCAAAAAGA[A/G]ACAGCTGAGTCTCCA	84182
rs571558523	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30826123	AATTACATTGGTCCC[A/G]TTTAGGTAATATAGG	84182
rs571575966	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30800275	GCATTGGATGCCCTG[G/T]TGAGATGGGCCAAGC	84182
rs571600775	in-del	-/TG	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30787761	ATCTGCTGGGGACAC[-/TG]TGGAAGGAGCCCTGC	84182
rs571669805	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30832656	CTGGGATTACAGGCC[C/T]GTGCCACCACACCTG	84182
rs571673924	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30797830	GCAGTAGTAGAAGAG[A/T]GCTGGTGGTGGCTTG	84182
rs571682742	in-del	-/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30844944	AAGTGAGTAGGGCCA[-/T]TGAACTCAGCCTGCC	84182
rs571723331	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30770824	GAATCTCAGTGTCCC[A/G]TTTTAAAGAATGGGG	84182
rs571781060	snp	G/T	0.0023933	0.0345097	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30835839	CTGTGTTCTGGTGAA[G/T]GCAGCGGCAGCAGGT	84182
rs571783033	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30800252	TGTCCCTGGATATCA[C/T]CTTAGATGCATTGGA	84182
rs571786756	snp	G/T	0.0023933	0.0345097	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30871162	GTCATGTGCAGAAGT[G/T]GGGGGGACAGACCTG	84182
rs571812385	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30794043	GGCACACAGACTGGC[A/G]AATGGAATATGGGCT	84182
rs571817132	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30860783	CCAGGCCAGTCTTCA[C/T]GTTGTGCACAGCTGG	84182
rs571832209	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30799423	GGAATCACTCCCAGC[C/T]CTGAGTATGAGCATC	84182
rs571845099	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30876789	CAAAGATTCTTGGAG[G/T]GTCCGGATGAGGCCT	84182
rs571851663	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30883736	ACCCAGAGGCCTCAG[A/C]GTGCATGAGAGGAGC	84182
rs571864586	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30847489	CCACGGCAGTTGGTT[C/G]TACTTACCCAAGCTC	84182
rs571962657	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30890520	CAAATGACAAGAAAT[A/C]TTTCTGCTCATTCAA	84182
rs571966907	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30777500	TCCTCTTTCCTCTGT[C/T]TGTTTCAAGATTGTG	84182
rs571968117	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30838598	CTTTGCTGTGTGCCA[A/G]TAGAACATTATTTAC	84182
rs571979648	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30871659	GGTACCAGGGGGTGG[A/G]GGCACAGGCCTCAGA	84182
rs571981646	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30848298	GTGTATGTGCAATGG[C/T]GATTGGACGGTGGGG	84182
rs571993424	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30834260	CCTCTGAAATCTAGG[C/T]GGAGGTTCCCAAACC	84182
rs572018615	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882416	CAAGGAGCCTCCAGG[C/T]TGGTCACAGAAACCA	84182
rs572029299	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30838355	CCCCTTCACTGGGGG[G/T]TTGGGATGGTTCAAG	84182
rs572082477	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30813916	TCATGATGGGGCAGT[A/G]TAGGGTGGAAGGAAG	84182
rs572082567	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30821607	TTTCTATGAGAATGC[A/G]TGTCTGGAAAGTTCT	84182
rs572121066	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859465	AATGAAGCAGTGGAG[A/T]AGGGGAAGGTCTGCT	84182
rs572125996	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782543	CCTGTCTCTACAACA[A/G]CAACAAAAAATTAGC	84182
rs572140906	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30820622	GTCAGGCTTCTTTCA[C/T]TTAACATAATGTTTT	84182
rs572150577	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30847442	AAAGACAGGGTCAAA[A/G]GCAAAGGAGGCTGGT	84182
rs572183498	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30874883	GTTATGTAAGATGTT[A/T]TCGTTGGGGGAAGCT	84182
rs572188405	snp	A/G	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30827662	ACTGCCTGGGAGGGA[A/G]GGTGAGGGAGTTCTG	84182
rs572210235	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30790388	ACTGTAAGCAGCCTC[A/G]CAGCAGTTAAGAATT	84182
rs572232149	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30866274	GCAGGGCCAGGTGCG[A/C]AGAGAAAGAGGACAG	84182
rs572250135	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30789350	AGGTGGTATCTGAAA[A/C]CCACAAAGGATGTTG	84182
rs572251455	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30797210	GTGTGCCAGACCCAC[C/T]AGCCAGTCAGCTGTG	84182
rs572263954	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30796479	GTCCATGCAATTGAA[A/G]TCTAATTTAGACTTT	84182
rs572317770	snp	A/G			upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30770862	TAACTACCTAGCCAG[A/G]AAGTTGTAAGGATTA	84182
rs572323843	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30869049	GAGGGGCCCCCAGTG[C/T]AGGACAGCTTCCATT	84182
rs572338536	snp	A/C	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30788777	TGGTCGTGCAGTGCC[A/C]GCTGCCATCCTCCAC	84182
rs572375360	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30794845	AGTCCTCTAACCCTC[G/T]TCTCTCTCTCCCTCT	84182
rs572383675	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30784491	CTTCCCCTCAAATCC[A/G]CCCTTGCCCTAAGAT	84182
rs572387992	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30822310	CCTGTAGATGGGACT[A/G]CAGGCTCACACCACC	84182
rs572434234	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30794411	CCACCGCTCTGTCCT[A/G]AGGAAGCTGGAGGAG	84182
rs572439085	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771435	CTGCGCCGGACAGAC[C/T]CAGTTGCCTGGTGCT	84182
rs572440891	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30885133	ATTTGTGTAGCACAC[A/G]GGGGCTAAGAGGAGC	84182
rs572442055	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30862282	AGGATGGGAATAGCC[C/T]GGGCAGTCGTGGCAC	84182
rs572449317	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30829233	CTGTGTAACTGCTCT[C/G]TAAGATCAATATAGA	84182
rs572507316	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30803032	CATTCCATCCAACCA[A/G]CTAACCAACCCACCC	84182
rs572509332	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30873429	CAGTCTTTTTCCCCT[C/G]CTGTGTGTCAGTTTC	84182
rs572528928	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30834925	AGACCTTATTGTTCA[C/T]ACTACTATCCGCATT	84182
rs572571072	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30809426	TAACCACTGAAAATT[C/G]CCTTAACCCAGCAGG	84182
rs572591296	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30862089	GGCTTCAAGTGAGGA[A/T]CAGGGCAGGCCTTGG	84182
rs572592187	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30834503	CTCCGGGTCTGTGAT[A/G]GGAGGGCGTGCCATG	84182
rs572595593	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30798535	AGAGTCTCGCTGTGT[C/T]GCCCAGGCTGGAGTG	84182
rs572621055	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30802548	TCAGCCATGTCTCTG[C/T]ACCTGGCAATAATAA	84182
rs572643403	snp	C/T	0.0023933	0.0345097	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850609	TCTGCTGGCAGCTGC[C/T]GGCAAGCTGGCTGTG	84182
rs572658702	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30798901	CACACATGTGAGCAG[C/T]GAGCTGTCCTGTTAC	84182
rs572689020	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882657	TTCTTCAGGCAGTGG[C/T]GAGCCATGGAAGGTT	84182
rs572692370	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30844688	TGGGTGGGTGTCTAG[C/T]CTGTAGATGTTGGTG	84182
rs572702934	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850283	TCAGCTGTGGAGACC[C/T]CTCTTTCCTGGGCTT	84182
rs572709650	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839421	AGCATTAGCTGAGCT[A/G]TTCTGGACCAGCCAG	84182
rs572715982	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30889356	CTGGGGTCAGCACAA[G/T]GCCTTCCCAGCCTGC	84182
rs572732795	snp	G/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30787400	AGATTTGGAGATGTT[G/T]AATCTTGTGGGAGGT	84182
rs572737136	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30825649	TTCTAAGTTGTGTGA[C/T]CTTGTGTAAGCCACC	84182
rs572751689	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30871622	CTTTTGAAGGACTCC[A/G]TTCTGAGGGTGGAAC	84182
rs572765356	snp	C/T	0.0023933	0.0345097	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30871196	CCCAGGCTCCCTGGT[C/T]TCACGTTGCCCCCCA	84182
rs572838658	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30888008	ACAAGAGGCGTCCCT[A/G]GATGCTTTTCTACCA	84182
rs572878387	snp	A/G	0.00358779	0.0422022	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30876346	CTCCAGTATGACCTC[A/G]TCTTAACTAATTATG	84182
rs572880227	in-del	-/T/TT			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30817366	GAACTTGGGTTTGTC[-/T/TT]TTTTTTTTTTTTTTT	84182
rs572915301	snp	C/G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836469	ATGGACTCTCTTGAT[C/G/T]TGGTTGCTTTCCTTC	84182
rs572930709	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30843042	CACATCTGCCGCCAC[A/C]TACTACTGCCCACCC	84182
rs572947625	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30806025	AACGATAATTGATGT[C/T]TGTAATGATGGGCCC	84182
rs572972934	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30805426	CAGATCCCAGGGAAT[G/T]TTGGGAGGAGCTGGC	84182
rs572983197	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30789729	GTCCAGGCTTTACTA[G/T]TTGGTCTTGGATTAT	84182
rs573026878	in-del	-/T/TTCT	0.261608	0.24973	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30877683	TTCTTCTTCTTCTTC[-/T/TTCT]TTTTTTTTTTTTTTT	84182
rs573033954	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30813167	TTCAGATCCTTAAAA[A/G]CCAGAGAACCAGAGC	84182
rs573045080	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30847070	ATGATGCTTTGGGGG[C/T]ATCTGACCCAGTGTC	84182
rs573087954	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30811394	ATCGCTACCTTCATT[C/T]ACCAAAATGCTTCAG	84182
rs573095325	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30812678	AACAACAGCTTGCAC[A/G]TGTTTTCCAGGTGCA	84182
rs573108795	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30841310	TCCATTTCACACATT[A/G]AGTGTTTGCACATGA	84182
rs573109362	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30819206	GCCCTCTCCATATTA[C/T]TTTAACTGCTTCCCG	84182
rs573110723	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30816406	TCAGATCTTGCTCTG[A/G]CTCTGCATACTTCTT	84182
rs573148451	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30801216	CTTCTGAGCATCCCA[A/G]CTCTGAAAACATCTG	84182
rs573152825	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30789641	TGTCCTGAGTGGCTT[C/T]GGGAGGAGGTTTATA	84182
rs573158789	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30812546	TGCTGGAATCTGGGT[C/G]AGGTGATGGTATAAA	84182
rs573169774	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30818408	TTATCTCAACTAACA[C/T]GTAGCAATTTCTGTA	84182
rs573236643	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30877540	TGCCTTGCAACTGCA[A/G]GCTCACTAAGGAAGG	84182
rs573279042	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30849118	CACTGGCTATGTGTC[C/T]CAGGCACTGGGCAGT	84182
rs573290362	snp	C/G	0.00398564	0.0444627	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30807135	GAGACCAAGTATTTT[C/G]CCACCATCTGAGGAT	84182
rs573293343	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30854118	GACTCTGTGGGGAGG[G/T]GCTACACACTCCAGG	84182
rs573298135	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30883869	GCCCTGGTGTTGCTG[C/T]TTCTTGGTGTGAGCC	84182
rs573323043	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853588	GAGGAAGCTGGGAAG[C/G]AGTAATGCTGGCCCC	84182
rs573326091	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30889769	ATTTTCACTTCAAAA[C/T]GATTGATGAAGGGGA	84182
rs573327866	snp	C/G	0.00398564	0.0444627	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30845933	TTTTCCACTTGAGAA[C/G]AGGCTGTGCCGGCTT	84182
rs573331554	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30842956	CCTCCCCCATTAAGA[C/T]AAAACCAGGCCCTGC	84182
rs573392533	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30845650	AGGCAGCCCCTGCAC[C/T]TTCCTGCCTGTGTGC	84182
rs573409572	snp	A/T	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30883371	GGAGGCTTGAGCAGG[A/T]TAGGAAGCTGGGAGG	84182
rs573431374	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30815821	CTGAGAGAAGGGCAG[A/G]GAGGTGTGAACTGGG	84182
rs573442627	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30781477	AGTCCTGACTGCCTC[G/T]CTGTGCTCTTCACAT	84182
rs573456157	in-del	-/A	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30787944	TAAAAATATTTACTT[-/A]CAAAAATCATTAAAA	84182
rs573456943	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30826242	GATATAATTGAGGGC[C/T]GTTATTCAGCCTATG	84182
rs573504232	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30822109	AATATTTCAGCATGC[A/G]TCTCCTAAGGGCAAG	84182
rs573537946	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30774987	TCTTGAATTCTTACA[A/G]CTGCCTATTCTACAT	84182
rs573571958	snp	C/G	0.00914312	0.0669923	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30810083	CAGGAGGCTGAGGCA[C/G]GAGAATCGCTTGAAC	84182
rs573582965	in-del	-/AG	0.00795532	0.062565	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30783816	GATTTTCGTAAAAAC[-/AG]GGGTATGGTATTCTA	84182
rs573586251	snp	G/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30863844	TCTCGAATTGCTTCC[G/T]GTAAATCTCATGCAG	84182
rs573616196	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30892296	TCCCTTGCTCCCTGC[C/T]GGGTGGTCCCTCACC	84182
rs573621506	snp	C/T	1.65663e-05	0.002878	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859284	CCCTATGGCTGCATC[C/T]TGCTCACCCTTTCTG	84182
rs573635811	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30803944	CCCTGTGATAGGCTG[C/G]ATGCCTTGGGGCCTG	84182
rs573654799	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30856785	CGAGACCAAGAGCTT[C/T]GTGACTTCCCTAGGC	84182
rs573665600	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30858357	TTCACAACTTGATAA[A/G]GGTAGGTGCTGTGAT	84182
rs573666613	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30880698	GTTTAGGCACGTCCA[G/T]CCACGTCCTGTAAGA	84182
rs573680702	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30886625	CCCAGCCCATTGGAA[A/G]GTCACTTAGTGGGCA	84182
rs573697006	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30803198	TCATGGCACATGTCA[C/T]GCTGGAGAGAGTTGA	84182
rs573713727	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30794087	CTCTCACTGCCTCAG[C/T]GAGGCGTCTTTGTGT	84182
rs573722457	in-del	-/TTGA	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836029	TCTGCCACTTTCCAT[-/TTGA]TTGATTTGGGGCCAG	84182
rs573741458	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30886085	AGGAAGGGGATACAC[A/G]TGACATCGTGGCATG	84182
rs573744026	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30856197	TTCCCAAGTGGCACC[A/G]CTTTCTAGACCCTGA	84182
rs573779652	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30772714	TGCGTTTGGCTTTGT[C/T]GCATCTGCCCTGTCT	84182
rs573813857	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30784418	TCAGTTCACACTCCC[A/G]TCCTCTTTTCCTGGT	84182
rs573816905	snp	A/G	0.00318978	0.0398085	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771971	AAGAACTTCTCCCAG[A/G]GGGAACCCCAAAAGC	84182
rs573821447	snp	A/G	0.00478085	0.0486577	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30820063	CCCGCCACTACGCCC[A/G]GCTAATTTTTTGTAT	84182
rs573879988	snp	G/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30891765	TCTCTGGGGTCCTAG[G/T]TGTATTTGTGTTTCG	84182
rs573900224	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778302	TATTAATTATTGCAA[A/T]GGTGATGTCAAGTGT	84182
rs573900292	snp	C/G	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30790871	AGGTGGTGATGCAGA[C/G]TGGAGCGACGGCTTC	84182
rs573905175	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778249	TGAAAACTTCAGCCT[G/T]CACTTAGCCCATGGG	84182
rs573957104	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30841005	AGCTGACAAGGCCTG[C/T]GCAGACCAGTGTTAA	84182
rs573958195	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30862216	CTAACCCTCCTACCC[C/T]ACCTGGAGCCCAGGG	84182
rs573975906	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30810972	ATACTTGGTTTATCT[C/T]CCACTTTTCTTTCCC	84182
rs573999022	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30779834	CAGATTGGATTCGTA[C/T]GGTGGTAGGACCAAG	84182
rs574028535	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30861431	GTTTTTCAGAGGAGG[A/G]AGCAAGGCTGAGGGA	84182
rs574096850	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785562	TCTTATTTTATAGGG[C/T]AGACTTGCCTTGATA	84182
rs574136329	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791736	TGTTATGGTCAACCA[A/G]GAAGAAAACTCAGCC	84182
rs574179661	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30848493	AGGAGCTGTGGGGGT[A/G]ATGGAGTCACATTTG	84182
rs574233600	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30798406	ACAACTGTAAGAGGG[C/G]GGTTGCCGTTCCCTG	84182
rs574245366	snp	A/G	1.65842e-05	0.00287955	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791409	TGCCCCCATGGGACA[A/G]GGCCAGGCCGAGGGA	84182
rs574309823	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30871716	CTTTTCTGAGGCTTG[A/G]TTTTCTCAAAGGGTT	84182
rs574313568	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828007	AGTTCAGGTCAATGT[A/G]TGCTGGAGAACAGAA	84182
rs574339607	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30781192	GGCGAGTGGGTTGGG[A/G]ACTGACACATGGCTG	84182
rs574342640	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30813353	TGTTCAATCCCCAGG[C/T]CCTGAATTCTGTGTG	84182
rs574366641	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30798267	TATAATCTTATGGAA[A/C]CACTGTGATATATGT	84182
rs574378837	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30829670	CTCTGCCTAACTGAT[C/T]CTAGAAGTAGCAGAT	84182
rs574388106	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30804549	AGGATTAAGAAAAAG[A/G]TGAGTGTGATAAGGG	84182
rs574425368	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30860336	GGGCTCTGTGGCCTC[A/G]TGCGCCAGGCTGCCT	84182
rs574428405	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30797792	AAGGCAAGTGTGGAG[G/T]CAGGGAGACCAGTTA	84182
rs574478394	snp	G/T	0.000447083	0.0149446	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828707	CTGCCGTCTGACAAG[G/T]TGGATGGTGAGCTGG	84182
rs574487169	snp	C/T	0.00318978	0.0398085	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30820062	GCCCGCCACTACGCC[C/T]GGCTAATTTTTTGTA	84182
rs574550984	snp	A/G	0.00279162	0.0372561	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30833232	ACCCGAGATTGGGCA[A/G]TTTTCAAAGGAAACA	84182
rs574571099	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30796430	CTGGAGAAAGTGAGT[A/G]TCTTCCCAGAATACA	84182
rs574584425	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30832690	AATTTTTGTATTTTT[A/G]GTAGAGATGGGGTTT	84182
rs574584917	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30810597	AGTAAAAACACGACC[A/G]GTTTTTCTTAAAGCA	84182
rs574591404	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30877487	AGCTGAGGACTGGGA[A/G]TTTTGTTTCCCTGCG	84182
rs574596339	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30837817	GAGTCCAGGTTCCCA[C/G]GCTCTGTTGACCACA	84182
rs574597208	in-del	-/CCCTGT			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30813324	TGGGAGGGAAACTTG[-/CCCTGT]CCCTGTGTTAAAGTG	84182
rs574614276	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30838257	GGGTTGATGGGAAAT[C/G]AACAGTGAACTCATT	84182
rs574614589	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872685	GAGATGATGGCCCTG[A/G]CCTCTTCTATGTTTG	84182
rs574617004	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30794315	TCAAGGGGAGACACA[C/T]ATGTGCACATATAAT	84182
rs574790148	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30873372	AGTCTGGGGCTGGGT[C/T]CCAAGCCCTGTTCTC	84182
rs574825783	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30834410	AGAGTGGCTGGGATG[C/T]AGGGCACCAAGTCCT	84182
rs574836511	snp	G/T	0.00318978	0.0398085	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30867666	CAATATAAACCCCAC[G/T]AAAGGGCTGTTATCT	84182
rs574838171	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839387	GTGGGTGTACCTCCC[A/T]GTTTTGGTTAATCCT	84182
rs574890444	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30808697	TGGCCATCAGAAGGA[A/T]GCCTGGACAGGTCCC	84182
rs574925129	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30878481	CTGTGACCCCACCAG[C/G]TGGTCTTGCCCATCT	84182
rs574971624	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30798836	CAGTGGTGTTTCTTT[A/G]TGAACTGGCCTTCCT	84182
rs574999591	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30844597	GGGCCTGGAGAAGAG[A/C]AGGGAGGTGGAGTCC	84182
rs575072384	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30770748	ATGTACTGGGCTTGG[C/T]TAGAAACCCAACTTT	84182
rs575087585	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30887944	GAATGGCTGGAGCAC[A/G]GGAACGGAAACTTTC	84182
rs575107822	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30813847	AAAATGCCCAGAAAA[A/C]AGTCATTTCTCTGTG	84182
rs575109224	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30810729	TTTTATTAAAACTAA[C/G]TTTAATATTAATAGC	84182
rs575112477	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30843904	AGGTGTGCCAGGTGC[C/T]AAGGAGCCAGACCTT	84182
rs575132561	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30876241	GTATCACTCCAGTCT[C/T]TGCCTCCATCCATCA	84182
rs575148138	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875790	AGTTAGAATCACAGA[A/G]GGCTTGGGAAGAAGT	84182
rs575155061	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836919	AAGAAAATGTGAACC[A/G]AGAGTCAGGAAAACT	84182
rs575174305	snp	C/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30849920	AGCTCATCCTTGAAT[C/G]TGTCCTGCCACTCAT	84182
rs575190741	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30779402	AATTTGTTATGAAGA[C/G]AGAAAAAGAATGGGC	84182
rs575201425	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30841229	CTCCCCTCTGCCAAC[A/G]TTCATAACCACACAT	84182
rs575231942	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30803493	AGATGGATGGTGCTA[A/G]TTGAGATGCCGTAGG	84182
rs575240866	snp	C/T	0.00358779	0.0422022	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30787617	CCTAGTAGCTCCAGA[C/T]AGCACAGCTGGCACC	84182
rs575272207	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882077	ACAAACGTGATCTTC[A/C]GCAGGGCCTCTCTGA	84182
rs575306061	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30812917	GGGTCCAGCTGCTTC[C/T]GATGGTTTTCCATTT	84182
rs575311017	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30841027	CAGTGTTAAGGGGAC[C/T]TGTGCGCGTTTGTTT	84182
rs575322147	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30847933	AGACAGAGTCTCGCT[A/G]TGTTGCCTGGGCTGT	84182
rs575347707	snp	A/C	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30811324	AATAGTAATAGAAAC[A/C]TGCTTACAGCTCCCT	84182
rs575387331	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30881519	CCTAGTTGTCTTTAC[C/T]GTGCAGTTCTAGTTC	84182
rs575401455	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30773796	CCCATCATAGCCCCA[C/T]GTAAACTCTTCTCCA	84182
rs575460411	snp	C/T	0.00478085	0.0486577	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30857597	CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA	84182
rs575497170	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30824904	TTTCCACCAAGCCAA[A/G]GATTCAGTTATTCAG	84182
rs575535945	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30772968	TTTCATTTCTAGCCT[C/T]TCCCACATCCCTCCC	84182
rs575560486	snp	A/T	0.00398564	0.0444627	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30824641	GTGGCTTGCGTGATC[A/T]TAGCTCACTGCAGCC	84182
rs575597264	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30792474	TTAAATATTTGGGAG[A/C]ATTTACTGGAGAAAT	84182
rs575666547	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850684	ATGCTGGGATGAGCC[C/T]TGCAAGCCAGCCTGA	84182
rs575703479	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30807620	CAGAAATGAAATCCA[C/T]AAGCAGACAGCCTGG	84182
rs575712035	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30830959	TGGGCTGGGCAAGAT[A/G]ATTTTGAGTGCTGTG	84182
rs575713139	snp	A/G	8.68319e-05	0.00658851	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859177	AGGCTGCTCCCTGGG[A/G]TGTGGCTCCCACAGA	84182
rs575713891	in-del	-/C	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30787988	ACCTGTTGCATGTAA[-/C]ATGGTATATTTTAAT	84182
rs575719066	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30810139	CGAGATTGCGCCACA[C/T]ACTCCAGCCTGGGCG	84182
rs575723861	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30818902	TACTGAAAAGCTCCT[A/G]TTGATAATGTTTAGT	84182
rs575726105	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30806232	GGCTCGCCATCTTTC[A/G]CATATTTAGTAACTT	84182
rs575730659	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850344	CCTCTGCAGGCCAGA[A/G]AAAGAACAGGCCATC	84182
rs575732788	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30856116	CACCTCTGCCTCCCA[A/T]TGGAGTTCCTTGGTA	84182
rs575742934	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30855571	ATTGCTCAAATGACC[A/G]CAGATCCTGAGGCTT	84182
rs575837756	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828624	AACAGTCTTCTCTGC[C/T]GTTTACATTTCTCTG	84182
rs575857460	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30787251	AGGAAGAGCCTTCCC[A/G]CCACTGTGTAGTTCA	84182
rs575900435	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30827754	CTGTGCGTCCTCTAG[C/T]TCTTCCATTCACGCC	84182
rs575932804	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30780716	GTAAATTGAGATTTT[A/G]AAAAACAATATCTAG	84182
rs575960573	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771887	GCGGGCGCACAGCGG[A/G]CAGGCCTGCGCCCTA	84182
rs576004329	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785530	ATCATCTCTGAATTT[C/G]TTTGCTTGTTTACTG	84182
rs576046272	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30864068	TGAGAAGGTCCAGTG[G/T]GGGTGAAAACCTTTT	84182
rs576056533	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30786071	CACGCCTGGGTTTAT[C/T]TGGGGTACCCCACAG	84182
rs576060424	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30809491	ACAAAGGCCCGACCA[C/G]ACCTAGGAGGAACCC	84182
rs576085982	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30822034	GTATTTATATATACA[C/T]GTATTTTTCTGATGA	84182
rs576112510	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30869607	TGTGAGTGTGCATCT[C/T]TGGTGTCCCTCTATG	84182
rs576114987	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30814700	CATAGAAAGGTAAAT[C/T]AAAGCCCAGGGAAGG	84182
rs576127685	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30891711	AAGTAGGTTGTGGCA[C/G]AAAAGAATGCATCAC	84182
rs576159556	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30861360	TGCACATGAACGCAT[C/T]GAGTCCACAGCAGCC	84182
rs576164497	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30891357	AACTGTTATTCAGTT[A/G]TCTCTAACCCTGGAC	84182
rs576170361	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30869156	AGGGCCCAGGGTCAT[C/G]CAGCCCCCAGGAGGA	84182
rs576279998	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30783855	ACAGAACACTGCAGA[A/G]ATGGGAAAAATCTGG	84182
rs576288962	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30845894	CAGTCGGGAAGGATG[A/G]AGCTGGGCAGCAGTA	84182
rs576307679	snp	A/G	0.00398564	0.0444627	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30796289	AAAAGGCAACAGGAA[A/G]CCCACAGCCATGCCA	84182
rs576336613	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30857198	TGTGGACCTTTGCAC[A/G]TGCTTCTCCTTTTGG	84182
rs576345066	snp	A/G	0.00318978	0.0398085	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30880244	CTAATTGTGCTACAT[A/G]TTCCCCCACCAGGAC	84182
rs576368911	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30783284	TGTGTTGTTACATCT[A/C]CTAACTTTACTACCT	84182
rs576369001	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30790158	TCCCTACAGTCTTGT[A/T]GGGGAGAAGTACTAC	84182
rs576390182	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30823196	GGTGTATGTCACTCT[A/G]TCTATCATTGTAAAG	84182
rs576405180	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30789454	CTTATTGGTTGCTCA[G/T]GAGAAAAGCTCCAAA	84182
rs576406623	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30788549	TTGCAAAGCTCTCAA[A/G]CTCACGGTGGCAGAT	84182
rs576450936	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30873244	TGCCCGGGGTGGCCT[C/T]ACTCTCACTCCAGGC	84182
rs576466677	snp	A/G	0	0	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30862841	CTAACAGGAGGGGTT[A/G]GTCTGGTGCTTTTTT	84182
rs576466891	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30792258	CTTGGCTATGATATA[G/T]TATCTTTTTATATAT	84182
rs576476003	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30818632	GGTGGTTCCAGAGTC[C/T]GAGTGTACTCTATTT	84182
rs576562455	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30802581	GCCAAGCAAATGAGA[A/G]AGTGCACTTAGCAAG	84182
rs576566768	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30790967	CCAGCAGGCGGGGTG[C/T]GCATCACTGAAAGCC	84182
rs576578678	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30880609	GGTCCCTGTGTCAGG[G/T]TTCCCTGTTCCTGGC	84182
rs576599289	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840519	ATGAGGAGTCACTTT[C/T]CTCCCATGACACACT	84182
rs576629295	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840241	CACCACAGGGTGAGA[A/C]AGGACAAAGATACAC	84182
rs576646498	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30876458	GTTCAACCCATAGTA[A/G]GCCTCACACATCCTG	84182
rs576683792	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30849961	CTGTGTCTAAATGTC[C/T]AGCAAGTGAGGCTGC	84182
rs576691160	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30861755	TCAGATGGCTCTGTG[C/T]GTCTTCTTGTGTTTC	84182
rs576703414	snp	A/G	0.00358779	0.0422022	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30880083	ATTGTCTCTAGCACT[A/G]TGTCCCCATTGCTGT	84182
rs576742119	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30866173	GGCCACACCCAGGCC[A/G]CTGAAGAGCTGGGAG	84182
rs576764658	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30826906	TGCTGTTATTTTAAT[A/G]CATGTGATTATTGTT	84182
rs576786451	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30803785	CCAGCGTGTTTTTCT[A/G]CGGCCTGCATTGGGT	84182
rs576805942	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30833902	CTCCATGTCTCACAT[A/C]TAGGTCATGCTGATG	84182
rs576846545	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30865518	CTGGTCCCGTCCCTG[A/G]GAGCCACCTGCTCCT	84182
rs576865662	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30845757	GCAGATGGAGGATGG[A/G]ATCGCACCCTCCAGG	84182
rs576874352	snp	A/C	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30794221	CCTCCATCAGTGCCC[A/C]CTTCCCCTTGTTTTT	84182
rs576874939	in-del	-/G	0.00557542	0.0525036	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785316	CCCATTGGCACACCT[-/G]ACTTCAGCTTTAGCT	84182
rs576909434	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30788870	GCTGGAGAGTCTAAG[A/G]GCATAAAATGAATAA	84182
rs576952344	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30793756	TCTAAGAGGAAAAAG[A/G]GTAAAGCTGAGCCTA	84182
rs576959774	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30808115	CGCAGATCCTGAGAG[C/T]GCTCCCGGGTAGGCA	84182
rs576970094	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30790527	TCTCGGCTCACTGCA[A/G]TCTCTGCCTCCTGGG	84182
rs576976055	snp	C/T	0.00318978	0.0398085	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30807792	TGCAGCCCGCAGTCA[C/T]GTACCCCCTGCTTGC	84182
rs576987564	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30883144	AGACACAGGTTTCTC[C/T]ACTCGTGGTCACTGG	84182
rs577012509	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30842453	TGCTAAGTAAGAACC[A/G]CTGGCTGCCCTCAGA	84182
rs577036312	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30874970	AAATTATTTCAAAAT[A/G]AAAAGGTTTCTTTAA	84182
rs577038057	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30813250	AGGGATTGTGCTGCT[G/T]CGATTTTTTCTTTTC	84182
rs577093607	snp	C/T	0.00398564	0.0444627	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30837784	GGAGGGCCCAGGGCA[C/T]GTGGCCTCTGGAAAG	84182
rs577094431	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882742	TAAAGTGGGACACGG[A/G]TGGGGACCAGTGAGT	84182
rs577109226	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30888961	GCTTGCCAGGATTCA[A/G]GGAATTTGTAACTTG	84182
rs577130586	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30795695	TGAAGGATGTCTCAC[C/T]GGTCTGCAATCCAGG	84182
rs577145343	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30877217	TCAGCTCAAAATTCC[A/T]TGGGCCAAGAGAGGC	84182
rs577157006	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782339	GTCTCTGTGTGTGTA[C/T]GTTTGTGTGTGTGTG	84182
rs577198020	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30835923	AGGCCTCAGTTGTCC[C/T]ACTATGAGAAAACAA	84182
rs577226887	snp	C/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30843847	TGGGCAGAGGAGGAG[C/G]GAAGAAGGAGCTGCT	84182
rs577247171	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30806187	TTTGGGAAACATTGC[A/T]TTGTATTGTATTCTG	84182
rs577265647	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30878979	TGTCCCCATCGCTTT[C/T]CCCCTTTCCAATCCT	84182
rs577288497	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30843174	TCAGAATTTTTGTTG[A/C]GAGAACACATGGACA	84182
rs577292405	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30770687	GTAACATGCGGAAGT[G/T]GCAAAGATTGTGAAG	84182
rs577313684	in-del	-/T	0.00199481	0.0315187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872504	AGAAAGAGAGCTCAG[-/T]TTAGCTTCTGTTTCT	84182
rs577330584	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30878425	CTGCCATAAGTAACT[A/G]GTCCGGCCTGGCTGT	84182
rs577354813	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30810617	TTCTTAAAGCACTAA[C/T]CTGCTCTATAACAAA	84182
rs577359036	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30883907	CTCACCTTCCTGCAC[C/T]CCACTTTGTCATCTG	84182
rs577379787	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30845780	CCTCCAGGGAAGTCA[C/T]GCTGAAATAAAGGCA	84182
rs577415586	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30816520	ATGGCTTAGGAGGCT[A/G]GAGTACAGCATGTGT	84182
rs577415617	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30810125	AGGTTGTGGCGAGCC[A/G]AGATTGCGCCACACA	84182
rs577423680	in-del	-/T	0.00358779	0.0422022	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30820957	ATTAACTGAAATGTA[-/T]TTTTTTTCTACTCTT	84182
rs577427245	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30815945	AATATCCAGCATGGG[A/G]TAGATTAAAATAAAC	84182
rs577478433	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30860269	GTTGGGTCTGGTCGG[C/T]GCCCTCCCTGTTTCC	84182
rs577483537	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30870535	GGTTCTCTGCAAGCT[C/T]CTGCAAGGGTAACCC	84182
rs577494795	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30820002	CGCCTCCTGGGTTCA[C/T]GCCATTCTCCTGCCT	84182
rs577505638	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30775591	GTTAGCTCAATCTAT[A/G]GCTTCTCTTCCCTCT	84182
rs577526202	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30798428	CGTTCCCTGAAATGA[A/G]GACTGTGGGAGAAGC	84182
rs577545092	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30854792	GGCAGCACCAGATGT[C/T]CCTTGGGTAGGCAAT	84182
rs577548944	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30849194	CTTTTCTCCTGTCCT[A/G]GAAAAGAGGGACGAA	84182
rs577589867	snp	C/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30804905	GAAGAATCCCAAGCC[C/G]AGGGGATGCTGTGAG	84182
rs577602193	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875355	GGGAGAATTGAAGTC[A/G]CAGCCTCCTCTGCTC	84182
rs577611199	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30854188	TGAATCTAGATTCAC[C/G]CTTCAGTAGCTCCCT	84182
rs577649302	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853184	TAGGGCCACCTGAAC[C/T]CTGACGACTCCAGCG	84182
rs577670388	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875025	CCAAATGTCACTTCT[C/T]CTTAAAGCTGCCCTG	84182
rs577677106	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30820147	ACCTCGTGATCCGCC[C/T]GCCTCGGCCTCCCAA	84182
rs577688414	snp	C/G	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30846021	AGGCCAGGAACGGCC[C/G]TCAGAGGCGGGTGCG	84182
rs577696225	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30773688	CTGCCACCCTGCCCC[A/G]TGGTCATGAGCTGGG	84182
rs577710790	snp	A/G	0.000108867	0.00737711	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859060	CACCCTCGCTCTGCT[A/G]TCATTGTCATTCAGG	84182
rs577723329	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30858380	GCTGTGATTATTACC[C/T]TCTTTTTACAGATGA	84182
rs577737046	snp	G/T	0.00318978	0.0398085	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30827443	CATGGGTGGGGGTGC[G/T]CTGACACAAACTCAG	84182
rs577740827	snp	C/T	0.00199481	0.0315187	downstream-variant-500B	FAM188B, INMT-FAM188B	GRCh38.p7	7:30892873	GAACATGCAGAAGTG[C/T]GGTGGCCTGCTGATG	84182
rs577773355	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30789472	GAAAAGCTCCAAAGA[G/T]TGTTGGGTATTTCAT	84182
rs577785458	snp	C/T	0.000399281	0.0141238	splice-donor-variant, downstream-variant-500B	FAM188B, INMT-FAM188B	GRCh38.p7	7:30892388	AATGGGTCAAACCCA[C/T]GTCAAGGGCCCAGGC	84182
rs577851101	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30794840	TGGGCAGTCCTCTAA[C/G]CCTCGTCTCTCTCTC	84182
rs577862715	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30831195	ATTTCAGGACCTGCC[C/T]GAATTTCACCTGTTA	84182
rs577868341	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30862782	GCGCAGCTCAGTCAC[A/C]CACAGCCGTGTGGCT	84182
rs577905296	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30797469	CAGAAAGGAGACAGG[C/G]AACTTGCACTTTGAT	84182
rs577929118	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30772865	TAGAGAGGGCTTCCT[C/T]GTGTTCTTTCTTGAG	84182
rs577938020	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30888413	TTACCCAGCCAAAAT[A/G]CCTTAGGTACCGAGG	84182
rs577945013	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30857449	CCAAGAGGAGAGATC[C/G]ATATCCACCTTGTTT	84182
rs577978299	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30818035	CTTGTTACTGACTCT[A/G]GCAGGGATGCTTCCA	84182
rs577996564	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30856822	CAGAGCTGGTACAAG[A/G]GACTGGTGACCCAAG	84182
rs578046455	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30795504	GAGGGTTCTGAGGCC[C/G]AGAGAGGGGCACAGA	84182
rs578055178	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30864547	CTGTCCCAGCTGCAT[G/T]CTCAGGAAGGTCCTT	84182
rs578067972	snp	A/T	0.00119737	0.0244387	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30812020	CATTACTACTGATTT[A/T]TTATTCTTCTTTTTA	84182
rs578078497	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30811550	CCCTCATATTGTCTT[A/G]TGCCCGATTTCTGCT	84182
rs578088171	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30864046	CCTGGCCAGGTCATT[C/G]AGGCCCTGAGAAGGT	84182
rs578159272	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30864401	TCAATTCCCAGCCAG[C/T]GTAAGCAGAAACAAA	84182
rs578172107	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30830549	TCACATGGTGGCAGG[A/C]AGGAGAAGTCCCCAG	84182
rs578177540	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30870439	ATGAGTCACTCCCAG[C/T]TGGCTCCTTCCCAGG	84182
rs578228781	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30798799	CACTGCGCCCAGCCC[C/T]GCATCTTACTTTCTA	84182
rs578233220	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30867141	CCAAAGGTCACGCAG[A/T]GCAGGTGGCAGAAGG	84182
rs578241060	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785637	TGGTTAGAAGTCATC[A/G]TAGATTTATTAATGG	84182
rs578241539	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30792644	AAATTTATTGGTATA[A/C]AATTGTATAATTATA	84182
rs578262174	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875723	CAATGAGGAGGGAAG[C/T]GGGGAAGGAAAGCTG	84182
rs745340505	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30863363	TGGTGGTGTGATAGT[A/G]TGTGTGCGGATGGGA	84182
rs745341959	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30838188	CTTTCTCATCTGAGG[G/T]CCTGTCCATGGGGAA	84182
rs745349670	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828003	CTTTAGTTCAGGTCA[A/G]TGTATGCTGGAGAAC	84182
rs745376324	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30797918	TACATACAGACATAC[A/G]TCAGCAGGGCTATGT	84182
rs745379716	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30796733	TTCCCTTGTAGTTAA[C/T]GTTTAAAGCTTTCTT	84182
rs745431996	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30837227	GCCCCGTGGTCACAG[A/G]GGACCAGGAGCAGGT	84182
rs745436069	snp	G/T	4.96882e-05	0.00498414	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828725	GATGGTGAGCTGGGT[G/T]CCCTGCGGCTCGGTA	84182
rs745501850	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853762	ACACAGGAAGCAGCT[A/G]TTAGATGGAGGTCAC	84182
rs745513465	snp	A/G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30773452	TCAAGTCTCTCCATT[A/G/T]CTTGGCTCTGGCTAC	84182
rs745527390	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30829925	TTTGAAGTGTGTGTG[C/T]GCATGTTTTCTGGAG	84182
rs745560380	snp	C/T	1.65603e-05	0.00287747	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785852	GGTGAAACTCCTGTG[C/T]TGACTTCTGCATGGG	84182
rs745563872	snp	C/T	1.68035e-05	0.00289853	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850592	GTTGCCGTGGCTCAT[C/T]GTCTGCTGGCAGCTG	84182
rs745572331	in-del	-/CAGTTCCTGCCAGCTTC	1.65688e-05	0.00287821	utr-variant-3-prime, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30892053	CTCATCACCTCATCA[-/CAGTTCCTGCCAGCTTC]CCGAGGATGACAGCT	84182
rs745644851	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30804403	TCAATCTAAATACAT[A/G]GTATTTAATTTTATT	84182
rs745650099	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30774870	TTCTCTTCTTCTTTC[C/T]GTTCACTCTCAAGAC	84182
rs745652613	snp	A/C	1.65669e-05	0.00287805	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859305	ACCCTTTCTGCCATC[A/C]TGTCCAGGTCTACAG	84182
rs745653417	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30816164	GAGGGAGCATCCATT[C/G]AATACCAATTGCGTG	84182
rs745686554	in-del	-/C/CCCCCC	0.00014915	0.00863458	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771565	AGAAAGGTAACGGCT[-/C/CCCCCC]CGCCCCCTCCAAAGC	84182
rs745696228	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30842717	AGGGCGGGCAGCCTG[G/T]TGGACTGACATTTTC	84182
rs745703965	in-del	-/GTT			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30890267	ATCAAAATTTCTTGG[-/GTT]GTTGACTAGGGAGCA	84182
rs745746260	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30834723	TGGATGCCTTTAACA[G/T]CACTCAAGTCGCCTC	84182
rs745747125	snp	C/T	0.000361171	0.0134334	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882365	GGCTGACCATTGGTG[C/T]GGGCCCTCACCCCCC	84182
rs745770834	snp	C/G	1.65767e-05	0.00287891	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785765	CATGACAATCTTGAT[C/G]GAGATGTACTTGGTA	84182
rs745812417	snp	A/T	1.74102e-05	0.00295039	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859207	AGGTGTGGGGCTGGG[A/T]AGAGGGAGGTGCAAA	84182
rs745815806	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882647	TTTGGATGTATTCTT[C/T]AGGCAGTGGCGAGCC	84182
rs745821267	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30870945	GCCCCCCAGGGTCGT[A/G]TGTGCCTCCCAGAGT	84182
rs745825597	snp	G/T	3.34353e-05	0.00408859	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882876	GACCTCAGGGTGAGT[G/T]CAGGGCCCTGGGTGA	84182
rs745842839	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30805530	TGGTGTGGGGCAGGG[C/T]AAGAAAACGGAGTGG	84182
rs745896434	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30877175	AGGGCTCTCGAGCAC[C/T]GGATCCTGGGTGTGC	84182
rs745906243	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30890215	TATGCCGAGTGTTTT[A/G]ACAAGAAGGTACAAT	84182
rs745922213	in-del	-/TG			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828321	CAAGAACTCGATTTG[-/TG]TGTGTGTGTGTGTGT	84182
rs745927305	snp	G/T			upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771134	GAAACAAGGAGGCAG[G/T]TATTCTTCCCATTTT	84182
rs745927974	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30801020	GTCCAGGGGGAGAGA[A/G]ACAAGTGCATCCCAA	84182
rs745928828	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30826687	TGTCTTTGGAGTTAT[C/T]GCCTGGGTTTAAATT	84182
rs745942487	snp	C/G	1.77027e-05	0.00297507	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875681	TGCTCACGTTCACCA[C/G]AAGTAGGGGAGCCTG	84182
rs745944756	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30812832	TTGTTTTGTCAAAAC[A/T]TCTGGACCTTTGATT	84182
rs745993354	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30783157	TGGTTCTGTCTGGAG[G/T]TTCTGAGGGGAAAAT	84182
rs745997869	snp	A/T	1.7151e-05	0.00292835	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882183	CTCCCTCATCCAGGT[A/T]GGCTGCTTCCTGAAG	84182
rs746012156	in-del	-/TT			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782342	CTGTGTGTGTATGTT[-/TT]TGTGTGTGTGTGTGT	84182
rs746019441	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30845280	AGAAGAGTACAGAGA[A/G]CAACATAGCAAACAC	84182
rs746034216	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30831424	CTAGTCCATCATGGG[C/T]GCTAAAGAATGCACT	84182
rs746045517	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30841581	GCAGGCCCGGTTACC[A/G]GCTTGTACCGAGTCA	84182
rs746071337	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30851537	AAGCACCACGTTTTA[C/G]ATATCGTTATTTGTT	84182
rs746090667	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30868020	CAGGGGCCGAGTGGA[C/T]GCTGGTGTTAGGTGA	84182
rs746100538	snp	C/T	1.6585e-05	0.00287962	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791396	CCCAGCAAACGGCTG[C/T]CCCCATGGGACAGGG	84182
rs746103376	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30878278	GCTTCTCACTGCAGC[A/C]TGGGGTTCTGGGGCC	84182
rs746153790	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30884348	GAGCCAGGGATGAAG[A/C]ATTCTTGCAGGGTCA	84182
rs746162457	snp	A/G	1.66125e-05	0.00288201	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836758	AATTGACCTCTCAGT[A/G]GCAAAGGTAAGTGTA	84182
rs746164377	in-del	-/ACAG			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30860999	CATACGTGGCCACAC[-/ACAG]AGACACACACACACA	84182
rs746188470	snp	A/G	3.31592e-05	0.00407167	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882974	CTTGTCCCACCCCTC[A/G]AGCTCTGCATCAGAA	84182
rs746208109	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30821219	ATTGTTTTTATTGTC[A/G]GTTCTCATTTAGGTT	84182
rs746216951	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30790921	TCTCTGTAAGGGCTG[C/T]GAGAGAAAGGCCCAG	84182
rs746259870	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30868981	ACCCCCTGGTCAAGC[C/G]CATCTCTCCTTTGTG	84182
rs746285444	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30856964	AAATAGGCCAGGTGG[A/G]TCTTCATTATTCTTA	84182
rs746287771	in-del	-/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30801846	AAGAAGTGAGAGAGT[-/G]GCCACACATCCCCCT	84182
rs746295957	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30819072	TAACTTTTTCATCTT[C/G]CATTTATTTTTCCTC	84182
rs746300157	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30832438	CACACATCTCTTTTC[C/T]TCCAGAGAACATTCT	84182
rs746319281	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30808122	CCTGAGAGCGCTCCC[A/G]GGTAGGCAACTGCCC	84182
rs746356749	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30886219	AGGGTAGGCCAGTCT[A/G]GTGGGCAGGTAGAAT	84182
rs746361944	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30815831	GGCAGGGAGGTGTGA[A/C]CTGGGAGGGCCACAA	84182
rs746380593	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778827	CTCAGCCTCCCGCAG[C/T]TATTCCCTGTGCTCC	84182
rs746396682	snp	C/T	1.85603e-05	0.00304628	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853420	CAGTTTGACCTGCTA[C/T]GAGGACCTGGTGACT	84182
rs746401549	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30846559	TTGTCACCTGGGTTC[C/T]GCCAGTGAAGGCGTG	84182
rs746420213	snp	A/C/T	3.35043e-05	0.00409283	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836632	AGTCATAACGAAGGG[A/C/T]TCACATGGCCATGGT	84182
rs746421100	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30885131	CTATTTGTGTAGCAC[A/G]CAGGGGCTAAGAGGA	84182
rs746435464	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30885290	TTTGGAAGGCCGAGA[C/T]GGGCAGATCACCTGA	84182
rs746487318	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30829916	AAGCAGCTGTTTGAA[G/T]TGTGTGTGTGCATGT	84182
rs746500215	in-del	-/A	3.40315e-05	0.00412488	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872310	TACTGTACACAGGTC[-/A]GGGGGCGCTGTGGGG	84182
rs746504275	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30816226	GGGAAATAATATGAG[A/G]GAAGGTCACATCTTT	84182
rs746506342	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30789906	TCAATTGACTCCTCT[A/G]GAATTCCTTCATTTC	84182
rs746511131	in-del	-/TT	1.65644e-05	0.00287783	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30891929	GAAGCTTGATCTCTC[-/TT]TGTCTCTCTCCTCAC	84182
rs746526563	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30787410	ATGTTTAATCTTGTG[C/G]GAGGTTGGCAGAATG	84182
rs746546887	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30799378	AGCACCTGTGGGTAT[A/G]TAGTAAATGGATTTA	84182
rs746558758	snp	G/T	4.73474e-05	0.00486533	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850580	TCCGAGGTCTGTGTT[G/T]CCGTGGCTCATCGTC	84182
rs746571733	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30865156	CTCCCGTCTCTGCAC[C/T]GACACCTGGCTTTGT	84182
rs746586636	snp	C/T			upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30770755	GGGCTTGGTTAGAAA[C/T]CCAACTTTCCCAGTA	84182
rs746609314	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882824	AGAGGAGGGGACAGG[G/T]ACTAGAAGGGGGCGG	84182
rs746630700	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30804650	GTCCTCACTATCTGA[C/T]TGGCCCTCTTATAGG	84182
rs746633233	snp	G/T	3.3413e-05	0.00408722	utr-variant-5-prime, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771461	GTGCTGCGGCCCGGC[G/T]TGGGCCTCGTGGGCA	84182
rs746641633	snp	A/C	1.83586e-05	0.00302968	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791135	CTCCCCTCAAAGGGT[A/C]CTCACTGCTTTTGTC	84182
rs746690586	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30854886	GCTTTCACCCCTCAG[C/T]CTGGGGAGAGGCCTC	84182
rs746734933	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30881592	TACTTACCCCGGGCT[A/C]CTGGAACTTAAGGGT	84182
rs746741808	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30874101	GTTTACACTGGTCAA[G/T]GGCCGTTCTGGCCAT	84182
rs746759709	snp	A/G	1.72368e-05	0.00293566	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782189	AGGATGGAGAACATC[A/G]TTGTCAGAAACAAGC	84182
rs746787327	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30805618	TGCATTTTCGGACCC[C/T]TAGGAGAGGTTGGGA	84182
rs746804949	snp	C/T	2.33049e-05	0.00341349	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882359	AGATCCGGCTGACCA[C/T]TGGTGCGGGCCCTCA	84182
rs746816968	snp	C/T	1.87591e-05	0.00306255	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859097	CAATGTCCCATCCTT[C/T]AGGAGGTCAGCCTTC	84182
rs746816987	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30772550	ATTGGATCTGACATA[A/T]AGATACAATGTGCAC	84182
rs746830038	snp	C/G	2.09593e-05	0.00323716	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859191	GGTGTGGCTCCCACA[C/G]AGGTGTGGGGCTGGG	84182
rs746840192	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30834816	TAAAGTTCTGCAAAT[C/T]TCTAGGGCAGAGGCA	84182
rs746857917	in-del	-/A			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30874983	TAAAAAGGTTTCTTT[-/A]AAAAAATAACATCGT	84182
rs746915000	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30825519	TGGCCCTTGTCCTGC[A/G]GTCTGCAGGAAGCCA	84182
rs746927827	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30889273	TCTCAAATGCTCATC[A/G]TGTTGCTGCAGATTG	84182
rs746940852	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30862073	TTGTAGTTAAACTGA[A/G]GGCTTCAAGTGAGGA	84182
rs746957222	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30861147	GGGGCAGTACAGGCC[G/T]CTGCCTCCCAGAGGG	84182
rs746967511	snp	G/T	1.95919e-05	0.00312979	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791615	GCTTTTCAAAAAGAA[G/T]CTCCACCTCTCACAT	84182
rs746992668	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30794940	ACACACCTGACCTGA[A/G]TAGACCCTCAGGAAA	84182
rs747007823	in-del	-/AG			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30812421	TTTTCAAAATAAAAA[-/AG]AGAATTAAAAAACAC	84182
rs747046823	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30802970	CAACCAACCTAACCA[A/G]CCCGGCCAACCAACC	84182
rs747053763	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30868462	GAGACTATGCAGATT[C/T]GAAGCCCATGCATTG	84182
rs747054330	snp	C/T	1.65679e-05	0.00287814	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840798	AGCTGTCCAAGGCTG[C/T]GTCCTACAGAAACTC	84182
rs747067271	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30815022	TTTAGTGTTTTGTGG[A/G]ACTCAGCCTCTCGTT	84182
rs747095675	in-del	-/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30841391	GGCACAAATGATACA[-/G]GGGAGAATTAGATGA	84182
rs747141268	snp	C/T	1.65696e-05	0.00287828	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778423	AGCGATTCAGCTTTC[C/T]TCCCTCAGGGCTTAA	84182
rs747155658	in-del	-/T			upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30769425	GGGGTTGGGGACCCC[-/T]GATACACAATCTCTT	84182
rs747167023	in-del	-/TT			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30818212	TATTTTTTAAATCTC[-/TT]GATATGAATTACATT	84182
rs747195473	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30833422	ACTTACTCACTATCA[C/T]AAGACCAGCACAGGG	84182
rs747214369	in-del	-/A			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30880665	TGAAGCATGGAATGG[-/A]AGCCAAGTTTACGTG	84182
rs747248224	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30869162	CAGGGTCATCCAGCC[C/T]CCAGGAGGACATGGA	84182
rs747248545	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30869327	GGATGGGACAAGCCT[C/T]CACACTGCCTTCAGC	84182
rs747296026	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30851181	AGCTGTGAGGCTAAG[C/T]GGTAGTATAAGGAGA	84182
rs747313673	in-del	-/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30849817	TCTGAAGTGTGACTC[-/T]TTTATCTTCTATCTC	84182
rs747352502	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30809306	CTTAGCTAACAGAAA[A/G]AATTTAAAAAATAAC	84182
rs747364519	snp	C/T	6.28871e-05	0.0056071	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853350	CAGGATGGGGCACTG[C/T]GTGGGGCTTGGGCCA	84182
rs747364647	snp	A/G	3.31362e-05	0.00407026	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828744	TGCGGCTCGGTAGGT[A/G]CAGCGGGTGCCTCTG	84182
rs747372451	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30780286	ACTTTAGGAGAATTT[C/T]GCGCAGAGAGTGAGA	84182
rs747378114	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30871856	AGACTGAGGCTCAGA[A/G]GTGGAAGAGGGTTCC	84182
rs747384285	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859757	GTCGCGTGGACAAGG[C/G]TGGCATCCTGGGTGG	84182
rs747425606	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30779418	AGAAAAAGAATGGGC[C/T]GTCCAGCAAATGTTG	84182
rs747437369	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30798004	GAAGGACCTGGGAGA[A/G]TTTGGGGTGCACCTG	84182
rs747442400	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30822843	GGGATGGGGTATCAC[C/T]ATGTTGCCCAGACTG	84182
rs747477976	snp	C/T	3.50042e-05	0.0041834	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875672	GTACCCAGATGCTCA[C/T]GTTCACCACAAGTAG	84182
rs747484902	snp	A/G	1.65605e-05	0.0028775	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778511	ACAGAAATGATCTTC[A/G]AAAGGTTTTGCATCT	84182
rs747503407	snp	C/T	1.65747e-05	0.00287873	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875606	AGAGGCATTGCTGCA[C/T]GCAGTGATATTGGCT	84182
rs747522339	snp	C/G	6.62548e-05	0.00575526	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852249	GTTCAGTCCAACAGG[C/G]AAATACAAAGCAGAT	84182
rs747526715	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30835773	AGTTCACTCTGCTCA[G/T]CCTTGCCGGCACCAT	84182
rs747531677	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30887786	GCTGACGGGGACCCG[C/T]GGGTGGCAGTCAGAG	84182
rs747538019	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30779267	AATGCAGTCTTTTTT[C/G]TTCACTATTTTATCC	84182
rs747552212	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30837298	TGCTCACCATGCTCG[A/G]CTACCAGGGTGGCCT	84182
rs747646353	snp	A/C	5.11252e-05	0.00505569	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872226	GCTGTGCTAACAATG[A/C]TTCTTGTGTTTTCCA	84182
rs747649695	snp	C/T	7.64789e-05	0.00618333	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850449	CTTCCTTTTCTTGTC[C/T]GCAGGGGACTGCAGC	84182
rs747659914	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30775326	ATAATGTGCTAGAAT[A/G]GCTCACAGAACTCGG	84182
rs747671942	in-del	-/G	3.33622e-05	0.00408412	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836645	GGCTCACATGGCCAT[-/G]GTTTTCTTTCAGAGG	84182
rs747679899	snp	A/C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30788673	ACTGATTTTCAAGAA[A/C/G]ATGCCTGCCAAATAC	84182
rs747707351	in-del	-/TAATTGTT			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30793168	ATTTAATTGTTTATA[-/TAATTGTT]TATGTATTATTCTTT	84182
rs747711081	snp	A/G	1.70232e-05	0.00291741	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872310	TACTGTACACAGGTC[A/G]GGGGGCGCTGTGGGG	84182
rs747724213	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30834030	TCTGTGGCTTTTCCA[A/G]GCACATGGTGCAAGC	84182
rs747752019	snp	C/T	1.66272e-05	0.00288328	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882905	GACATGTGTGTGCCT[C/T]TCTCCTCCTTCCCAG	84182
rs747765644	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30884122	TGGTGAGGCCCTGCA[A/G]TGCTTACTGCCTGAG	84182
rs747807179	snp	A/C/T	0.000132618	0.00814205	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882970	CGACCTTGTCCCACC[A/C/T]CTCGAGCTCTGCATC	84182
rs747846748	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30871956	TCTCTACCGTGTCAC[A/G]CTTCAGTCGCTGTTC	84182
rs747858581	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30845181	ACACCCACACAGACT[C/G]CTAGGGACCAAGGGG	84182
rs747942125	snp	A/G	1.66236e-05	0.00288297	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882270	TAGCCTGCAGCCGGG[A/G]CTCCTGCGTGACTGG	84182
rs747969600	snp	A/C/G	5.02166e-05	0.00501061	synonymous-codon, missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882207	CCTGAAGACCCCGAG[A/C/G]TTCCCCATCTGGGTG	84182
rs747990847	snp	C/T	1.65658e-05	0.00287795	stop-gained, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782064	GCTAACAATTTCACT[C/T]AAGATACCCCAATCC	84182
rs747999968	in-del	-/AC			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30861004	TGGCCACACACAGAG[-/AC]ACACACACACACAGA	84182
rs748001180	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30891391	AATTTAGTTATACTC[C/T]GTGCTTCTTCAGGTT	84182
rs748001656	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30862235	TGGAGCCCAGGGGAG[A/T]CTCCTGAAGAGGAAA	84182
rs748024641	snp	C/T	4.71887e-05	0.00485717	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853479	GAAGCATGCCTTACT[C/T]CTGTGGGATGTGCGT	84182
rs748084488	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30827046	AGGGGCCAAGGGTGG[G/T]TGACACTAAGGGTCG	84182
rs748104896	snp	C/G			upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771309	CCCACTCCGAGACGC[C/G]AGTTTGCGGGACGCT	84182
rs748122311	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30851248	GTTGGTCACTGTAGC[A/G]TATTGCTTCAGAGAA	84182
rs748122464	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30863084	AGCCCCAGCTCTGCA[C/T]ACACAGCTTAAAAAC	84182
rs748122481	snp	C/T			upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30770233	CACTTGGCAGTGAGC[C/T]GAGATTGCGCCACTG	84182
rs748128315	in-del	-/A			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839912	GGCAGAAAATAAGCT[-/A]AACCCAGGATCAAGA	84182
rs748133991	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30870833	TCCTCTCTAAATGTT[A/T]TACCTGGCCTCTCTC	84182
rs748151526	snp	A/G	2.38689e-05	0.00345455	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850515	GCCCTCGCAGACATT[A/G]TGTGGCGGGCAGGGG	84182
rs748152161	in-del	-/A	1.65711e-05	0.00287842	splice-acceptor-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859255	TTCTCTCCCCCTCCC[-/A]GTTTGAAGTGGGCCC	84182
rs748165935	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30784191	GGCACTTACTACCTG[A/G]CTGGGAAGTGAAATA	84182
rs748173325	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30779507	CACAATTTTTTAAAA[A/C]AGCAATAAAATGATA	84182
rs748179451	snp	G/T	1.6617e-05	0.00288239	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839234	TTGGTTCCAGCTTTT[G/T]CTGTTTCAATGAAGA	84182
rs748182789	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859031	ACTGATGCTCTCTTT[C/G]GTGGCCCCTGCATCA	84182
rs748216774	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30856655	CATGTATGTCCATGG[C/T]AGAAGTAGGCAAGAG	84182
rs748281823	snp	C/T	1.70985e-05	0.00292386	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839345	AGGTTTCCTTGGGAC[C/T]TTTCTGCTGGGCCAT	84182
rs748286803	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30781616	GTTCCCTACAGACTC[C/T]GTTTTTTAAATGAAG	84182
rs748298041	in-del	-/AA			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30809025	GAAAATCAAAGAGAG[-/AA]AGAAAGAAAGAGAGA	84182
rs748362556	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30860702	TCACTGGGAGTGGGC[A/G]CCTTGTTACATGCAT	84182
rs748368076	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30888119	CACTGGGTCCATCAA[C/T]GTTGAAAAGCAGTTA	84182
rs748435092	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30886550	TCCAGAATGGAGGTC[C/T]GTGTCCCAGCCACAC	84182
rs748447168	snp	G/T	6.33975e-05	0.00562981	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850599	TGGCTCATCGTCTGC[G/T]GGCAGCTGCCGGCAA	84182
rs748471823	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875888	GAAGATGGTTTGAAA[A/G]GGACTTCGAGGGATT	84182
rs748499358	snp	A/C	3.31257e-05	0.00406962	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875590	GAACATCACACTTCT[A/C]AGAGGCATTGCTGCA	84182
rs748499769	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30799618	ATCTCTGGACTGGCA[A/G]CATCTGCATCATCTG	84182
rs748547256	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30830135	GTTAGAGGAACAACA[C/G]TCCTCCTCCACCCCA	84182
rs748548574	snp	A/G	1.65641e-05	0.00287781	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852231	GGCTTCGAGAACACA[A/G]CAGTTCAGTCCAACA	84182
rs748554103	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30811436	TATATCAGTCACTAC[C/T]GATCTGTCTTGCAAG	84182
rs748556828	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30849824	GTGTGACTCTTTATC[A/T]TCTATCTCCAGCTAC	84182
rs748565817	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30781416	AACCTACTACTGAAG[A/G]CTTTCATTTGCCTTT	84182
rs748593068	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30838645	CAGATTTGGCCTGTG[G/T]GTCACAGTTTAGTAA	84182
rs748620692	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30865333	CCAGCCGAACTTTGA[C/G]ACTGATTCAGATTAG	84182
rs748631729	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30776924	GGATGGGACTGAGGA[A/C]TGGCTGACTCCCAAG	84182
rs748647761	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30866427	CAGGGCCTTTCTCAC[A/T]TGCAGTGTCACCTGG	84182
rs748655021	snp	G/T	1.65603e-05	0.00287747	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875518	CAATCTGCTCCTGAC[G/T]GGGAAAGCTGTGTCC	84182
rs748669166	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30849589	ATCCTACGACTGTGT[C/T]GTGGCACTCTCTCCT	84182
rs748682361	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30876867	GGGCCTTGCAGATAG[C/T]GCCAGGCGATTCCAC	84182
rs748721919	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30829336	AAAGACATGCATTTG[C/T]AGGGTTTTGCAGAAG	84182
rs748741163	snp	A/G	1.87005e-05	0.00305776	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882893	AGGGCCCTGGGTGAC[A/G]TGTGTGTGCCTCTCT	84182
rs748753786	snp	A/C	4.97162e-05	0.00498554	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785773	TCTTGATGGAGATGT[A/C]CTTGGTAATTTTGTA	84182
rs748760991	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872631	GACACAGGGAGTGAT[A/G]TCTCAGGCATGGGCC	84182
rs748761153	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30885039	CTTCTCTGCCCTCAC[A/C]TCTGCTTAGTGTTGT	84182
rs748809156	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30807306	ATCTAGGAATCAACC[C/T]CTGGATCTGCCAAAG	84182
rs748820864	snp	A/G	1.65611e-05	0.00287755	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785836	CATGCAGACGGTCCC[A/G]GGTGAAACTCCTGTG	84182
rs748831018	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30837185	TCTTCAGCACTGTTC[A/G]GGTGTACTCCCTTGG	84182
rs748838622	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30868645	TCTGCAAAATTCTGA[A/G]CCTTGCAAACTCTCC	84182
rs749022893	snp	C/G/T	3.31687e-05	0.00407228	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791405	CGGCTGCCCCCATGG[C/G/T]ACAGGGCCAGGCCGA	84182
rs749042845	snp	C/T			missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785805	CATCTAAAAGGCCCC[C/T]GCACAAAAGTAAGCC	84182
rs749051508	in-del	-/A	1.6585e-05	0.00287962	frameshift-variant, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791464	GACGGCAGCACAGAC[-/A]ACGGACAGGATGCCC	84182
rs749060440	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30786629	GACCCTGTCTCAAAA[A/C]GAAAAAAAAAAAAAA	84182
rs749063655	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30815345	TCAGAGACCACTGGG[A/G]AGGGAGGCTGGGCTG	84182
rs749073252	snp	A/G	0.000384221	0.0138551	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859146	AGGGCTGGGCTGGAG[A/G]CAGTTGGCTCAGGGC	84182
rs749146153	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30864018	CTGCTCTGGTGCCTC[A/G]GTGGAGCACAGACCT	84182
rs749146324	snp	A/T	1.65985e-05	0.00288079	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791474	ACAGACACGGACAGG[A/T]TGCCCTTGAAGCTCT	84182
rs749152510	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30827822	GTGCACCAGGGCAAG[A/G]TTACGATTGTTACTT	84182
rs749216938	in-del	-/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30891554	TGTCCCCATTGTTTC[-/G]CACTCAGCCATATCT	84182
rs749254846	snp	C/T	0.000116054	0.00761668	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840828	CCTGTTTGAAGGAGA[C/T]AGCAAAGCCGACTGT	84182
rs749259463	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30841943	AAGCCTAGGTGTTAC[C/G]CAGACAACAAGACCC	84182
rs749278392	snp	A/G	1.70933e-05	0.00292341	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872222	CAGAGCTGTGCTAAC[A/G]ATGCTTCTTGTGTTT	84182
rs749279358	in-del	-/AAA			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771576	CGGCTCGCCCCCTCC[-/AAA]GCCCAGGAAGTGGCT	84182
rs749303262	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30811628	AAGCAGACAGCCCAG[C/T]GCCACACCCTGGCTC	84182
rs749334582	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30804221	CTGTATGGCTAGATT[C/G]CATGTGTGTGCCTCA	84182
rs749362253	snp	A/C/G	0.000162374	0.00900919	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853451	TTTCTTCAACAAAGC[A/C/G]TTCATCAGGTATGAA	84182
rs749367642	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30860984	AGATATACAGATGCA[C/T]ATACGTGGCCACACA	84182
rs749415332	snp	C/T	0.000115721	0.00760572	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859027	GGTCACTGATGCTCT[C/T]TTTGGTGGCCCCTGC	84182
rs749424254	snp	A/C	1.66776e-05	0.00288765	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836777	AAGGTAAGTGTAAGG[A/C]GACTCCTGGGTTAAA	84182
rs749438239	in-del	-/A			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30809376	AGAAGTATCCTAAGG[-/A]AAAAAAAAAAAAAAA	84182
rs749442550	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839836	AGAAGCTGGGCCAGC[A/G]GAGGCCAATGGTTGC	84182
rs749443314	snp	A/G	8.06305e-05	0.00634892	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30781949	GCTGTATATAAATTA[A/G]TGATTTTTTTTTCTC	84182
rs749456589	in-del	-/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30783627	GATGTGAAAATCTTT[-/G]GGGGGGGTCACTATT	84182
rs749475603	in-del	-/A			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30885716	GCCCACCCCCCCCCC[-/A]AACCCTGCTGCCTTG	84182
rs749476476	snp	A/G	1.78535e-05	0.00298771	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875691	CACCACAAGTAGGGG[A/G]GCCTGACTCTCTGGA	84182
rs749476798	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30812641	GCAAGCTCTTGCACT[C/G]CAAGGAATCAGTGGT	84182
rs749532443	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850017	AGCACCTGCCTGTAC[A/G]TGCTACTGACTCCAG	84182
rs749533361	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30876093	TGGAGGCTGGAAGTC[C/T]AAGATCAAGGTGTCA	84182
rs749537815	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30837520	CCTTTCGTTTCCTTC[C/T]CCTCTCCTCCCCTCT	84182
rs749538095	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30854803	ATGTCCCTTGGGTAG[G/T]CAATGGGGCCTACCC	84182
rs749547397	snp	C/G	1.7603e-05	0.00296668	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791165	CCTTACTCCCTTTAG[C/G]ATTCTTTTCACAGAC	84182
rs749557749	in-del	-/AA			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30808970	GAGGCAGAGAGAGAG[-/AA]AGAGACAAATGGGAA	84182
rs749586167	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30889077	GGGACCAGGCTGAGA[A/G]CAGGCATGTTGCTCT	84182
rs749587668	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30888672	TTCGATTCGTCCCCT[A/G]CACTAGCACAACATG	84182
rs749588671	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30831038	GATACCTAGGGCTGC[A/G]CATTTGGGGGCTATA	84182
rs749614005	snp	A/G	1.71864e-05	0.00293137	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872324	CAGGGGGCGCTGTGG[A/G]GCCCAGGTGGTCCTT	84182
rs749626999	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30866590	GGTACCCTTAGGAAG[C/T]GGAGGAGAGATGGGG	84182
rs749658913	in-del	-/A			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785288	CACACACACACACAC[-/A]CACACACACACACCC	84182
rs749666092	snp	C/G	0.000186679	0.00965944	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850529	TGTGTGGCGGGCAGG[C/G]GGCCGAGAGAGAGCC	84182
rs749676726	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30800800	AGCCAAGGGCCCAAA[A/G]CCTCAGTGTTTCTGC	84182
rs749699561	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828097	CCTTTTAAGAAAGCT[C/T]TGTGTGCACATACCT	84182
rs749707796	snp	A/G	0.00016559	0.00909768	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875505	TGCAGGAACTTGTCA[A/G]TCTGCTCCTGACTGG	84182
rs749714156	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840544	CACACTGACAACTGG[A/C]CCCTTCCCCTAGGAG	84182
rs749736754	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30773555	CCAAGTGTGGTCTTC[C/T]CTCGGGGGAGTCATG	84182
rs749746164	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30796462	CCTTGAAGTATGATA[C/T]AGTCCATGCAATTGA	84182
rs749750112	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30845648	AGAGGCAGCCCCTGC[A/T]CTTTCCTGCCTGTGT	84182
rs749780779	snp	C/T	4.99048e-05	0.00499499	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839225	CCCTTCTGTTTGGTT[C/T]CAGCTTTTGCTGTTT	84182
rs749805419	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30789706	AAAATTAAGGTTTCC[G/T]TATTCCAGTCCAGGC	84182
rs749809871	in-del	-/AAT			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30851479	GAATAGCTGATAAAT[-/AAT]AATAATTGCGAAGTG	84182
rs749825188	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30867842	TCCCCAGGGTAAGTA[C/G]TGCCTGCTTCAGGCT	84182
rs749825304	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30856008	ACCAAGCCATCTTTG[C/T]CCAAAATCAATAGCC	84182
rs749834114	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30821303	ATTCAGTGAAGGTCT[A/G]TGATACTAAACTGTT	84182
rs749851352	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30887582	TTTGAAGCGTGAGCC[A/G]GCGAGGACCATGGTT	84182
rs749887008	snp	A/G	6.70893e-05	0.00579139	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875645	CTCTTTGAGCATTAC[A/G]ACATGTGCCAGGTAC	84182
rs749917802	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30842548	AAAAATGTGCAGAGT[A/G]TGCTTAGCAGGTCCT	84182
rs749923124	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30849450	ATGAAATGGAAAGAA[A/C]TACGTATATTCGGCT	84182
rs749924047	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30825175	TTGTTGTTCAGAATA[A/G]TTTTCACTCAAAGGC	84182
rs749934952	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30793520	TTCCACGCTCAGGCA[A/G]TCCTCCCACCTTAGC	84182
rs749940715	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30824174	AGGATGGGAGGTCAC[A/G]TCTAATGAGGGCCTT	84182
rs749950242	snp	A/G	1.65641e-05	0.00287781	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778550	TCTATAAGGAGAACA[A/G]GGTATGTGCTTTCTA	84182
rs749983513	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30888376	ATTTCATAATGCACA[A/C]CACGGTCTCCACAAC	84182
rs749987106	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30780012	GGCACCTACAGGAGC[A/G]CTCAGGTTGCCAGAA	84182
rs750069535	snp	C/T	1.656e-05	0.00287745	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875564	GTGGTTGAGCTGGAT[C/T]CTGGGGATGGGAACA	84182
rs750095171	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30888493	AGCACTGATGAATGA[A/G]TCTGGAACTTTGATT	84182
rs750131953	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30812059	AACTACAAAAGGGCA[C/T]GTGTACCAGATGCAA	84182
rs750196986	snp	C/T	1.65603e-05	0.00287747	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785834	CCCATGCAGACGGTC[C/T]CGGGTGAAACTCCTG	84182
rs750204876	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30776173	CAAGTGATCTTTCAA[A/G]AATATGTCAGTTCAA	84182
rs750217842	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30817105	AGAGGAAGCCCCTCC[A/G]GAGGCTCAGAGTCCC	84182
rs750225480	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30833207	ATTTTCACGCTGCTG[A/G]TAAAAACATACCCGA	84182
rs750236249	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30829816	TGCAGTGAAAGCTGC[G/T]TGTGTTTGGACACAA	84182
rs750248286	in-del	-/ATG			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30796663	GAGAACAGAAAGGAA[-/ATG]ATGACTCACTTGAGC	84182
rs750253542	in-del	-/AG			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30870675	GTTTTGGAAGCAGAC[-/AG]AGACTCAGGCATGTA	84182
rs750258931	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30800104	CTTAGCAGCTGACAT[A/T]GACAGCAGCTGGGAA	84182
rs750268328	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30865878	TGGACTGTGGGAGGG[G/T]TAACAGGAGCTGCTC	84182
rs750269237	snp	C/G	1.6676e-05	0.00288751	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30883029	GCTTTGAGCCTCACC[C/G]TGAATAGCTTTGAGG	84182
rs750273736	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30844867	AATAGTCATCTCTGG[C/T]TTGCCTAAATTGGAC	84182
rs750351168	in-del	-/A			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852416	AATCCTCATCCTGGG[-/A]TTAGGGTGGGGACAG	84182
rs750362668	snp	C/T	1.65745e-05	0.00287871	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828778	TGTGCCCATCAGGGC[C/T]CAAGGGGTCCTCGTT	84182
rs750394712	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30867172	GGCCTGACACCCATT[G/T]GTTCTGACTCATCGT	84182
rs750399016	snp	A/C			missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778483	CGCCCACGCTCTGAC[A/C]TCAGCATAAACAACA	84182
rs750435552	snp	A/G	4.33868e-05	0.00465741	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850486	ATGCCCACCGGACCC[A/G]CTGCCTCGTCCTGGC	84182
rs750437836	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30784051	AAAGCACTTCCTTTC[C/T]TGAGGGTCGCTGAAG	84182
rs750444608	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30789289	TGGACCTGCTTCACT[G/T]CCAAGGGCATTGCTG	84182
rs750469333	in-del	-/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30847566	GATCTGAGTAAATCA[-/C]CTGTGTCTCCATGCC	84182
rs750480301	in-del	-/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30846229	TGACCCTGAGAGGGA[-/G]CAGACAGGGAGCTCC	84182
rs750495102	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30827724	CTGAAGAAGTGTGTA[C/T]TCAGAGATTTGGTAC	84182
rs750524835	snp	C/G	1.66852e-05	0.0028883	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791517	GTAATTCCAGGATGA[C/G]CCAGGAGAGGCTGGA	84182
rs750553021	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30803871	AAAACCTAAGCTCAT[A/G]GCTCCACCTAAGGAT	84182
rs750567208	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30873891	TCCAAATTCTTGTGT[C/G]TCATTTCCTCTACAA	84182
rs750578453	in-del	-/TCCCC	2.12741e-05	0.00326138	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882397	ACCCACCCAACCCTG[-/TCCCC]AAGGAGCCTCCAGGC	84182
rs750582971	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30837008	TATGTCCTCCCCTCC[A/G]AATACCGTGGGAATA	84182
rs750583285	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30862838	TATCTAACAGGAGGG[C/G]TTAGTCTGGTGCTTT	84182
rs750587011	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30862825	GCCTTAGGTTCTTTA[A/T]CTAACAGGAGGGGTT	84182
rs750604656	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30773618	GTGACTCTTCTGCTG[C/T]CCCAGCTTCTTGAGT	84182
rs750634745	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30814837	TCTTTTCAAATGGCT[A/G]TGAGGTCAACCTTGG	84182
rs750649675	snp	G/T	3.40837e-05	0.00412804	utr-variant-5-prime, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771448	ACCCAGTTGCCTGGT[G/T]CTGCGGCCCGGCGTG	84182
rs750655633	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30891350	GCAACTGAACTGTTA[C/T]TCAGTTGTCTCTAAC	84182
rs750661697	snp	A/C	1.67835e-05	0.0028968	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872276	TGTCCCCACCAGCCA[A/C]CTGATTGGAGCACAT	84182
rs750663746	snp	C/T	1.65463e-05	0.00287626	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850409	CTGCACCATCTCAAC[C/T]TTGTGTCCACATGGG	84182
rs750675892	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30847024	TGGGGGTTGGGAACT[C/G]CTGGGTTAAAGACAG	84182
rs750677710	snp	C/T	1.65616e-05	0.00287759	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828695	AAAAATCAGTTGCTG[C/T]CGTCTGACAAGGTGG	84182
rs750739667	snp	A/G	1.65608e-05	0.00287752	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853509	TCACTAAGCCTTCTG[A/G]TTTCACTGTGGGAAC	84182
rs750755015	snp	C/T	5.10999e-05	0.00505444	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882318	TGACTTGTACTACTA[C/T]GATGGCCTGGCCAAC	84182
rs750762230	snp	C/G	1.66668e-05	0.00288672	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782142	TCAGAGACTACACTG[C/G]TAAATATATATGACC	84182
rs750765713	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30833143	TTATGTAAGGCCATG[C/G]TCATAGGGTAGCTTT	84182
rs750769437	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30854651	GGTTTGGTGGTAAGC[C/T]GGAGAGTGGGAGAAC	84182
rs750769605	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30877235	GGCCAAGAGAGGCAA[C/T]CTTGGCTAGGCTCAT	84182
rs750817745	snp	C/G	0.000106457	0.007295	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859158	GAGGCAGTTGGCTCA[C/G]GGCAGGCTGCTCCCT	84182
rs750834479	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30871201	GCTCCCTGGTCTCAC[A/G]TTGCCCCCCAGAGCC	84182
rs750859124	snp	A/G			missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875574	TGGATTCTGGGGATG[A/G]GAACATCACACTTCT	84182
rs750864689	snp	C/T	5.09654e-05	0.00504778	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839190	GTAAAACTCTCTCTT[C/T]TTTTTATAGGAAATA	84182
rs750871344	in-del	-/TG			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30790375	ACACTTTAAAAAGAC[-/TG]TAAGCAGCCTCACAG	84182
rs750875113	snp	A/C	3.31406e-05	0.00407053	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782019	CTTGAACTCATCACC[A/C]GATACTTTCTGGATC	84182
rs750880388	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30834113	AGCTCCACTAGGTGG[C/T]GCCCCCGTAGGGATT	84182
rs750888701	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30822524	TGTAGCCCATAATCA[A/G]ATCTTTCTCAAGTGT	84182
rs750990870	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791779	CCTGGAAAGCTGAAG[A/C]ATGCTCTAGACAGGG	84182
rs751001561	snp	C/T	1.6607e-05	0.00288153	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882259	AGCATCCTCTTTAGC[C/T]TGCAGCCGGGGCTCC	84182
rs751028070	snp	A/G	3.31417e-05	0.00407059	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791243	GAAGAGAGCCGGAAG[A/G]TCCCTGAGCTCTTTG	84182
rs751081117	snp	A/G	1.6566e-05	0.00287797	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791319	CCAGGACCTCCCTGG[A/G]TCAGCTTAGTGAACT	84182
rs751082658	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840433	AACACCCTCAACCTG[C/T]AGACACAGAAACATT	84182
rs751097172	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30783231	CTTGACTCTTGGCCC[A/C]TTCTTCCATTTTAAA	84182
rs751099184	in-del	-/TTTTTTTTTTTTTTTTTTTT			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30877828	CAGGGACATGCTTTT[-/TTTTTTTTTTTTTTTTTTTT]TTTTTTTTTTTTAAG	84182
rs751147664	snp	A/G	3.34325e-05	0.00408842	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839299	GCCTCATTAAAATAC[A/G]GCATAGTGCAGAACA	84182
rs751161356	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30867308	TCTGGGTTCTTGGCC[G/T]TGATATGAGTGGTTG	84182
rs751172452	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839467	GTTGTCACTTGGTGC[A/G]GGCACTTCAGATGTG	84182
rs751178419	snp	A/G	4.97133e-05	0.0049854	utr-variant-3-prime, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30892056	CATCACCTCATCACC[A/G]AGGATGACAGCTGAA	84182
rs751240398	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30817783	TGTGCGTGTCCATCC[A/T]CTTCCTATATGTCTG	84182
rs751253160	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30877999	CCCTCTTCTTTAACA[C/T]CACCTTCCATCCCTT	84182
rs751318989	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30883786	TGGATCCTGGTCCCT[G/T]CTGGGGGAGCAGTGG	84182
rs751347040	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30795808	TTCCTTGGCTCCCTT[C/T]CTTCACCTTTGAAGC	84182
rs751376020	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30818489	AACAGTCTTTTGAGG[G/T]AAGACTATTATTAGC	84182
rs751376715	snp	C/T	4.97517e-05	0.00498732	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785760	ACAGACATGACAATC[C/T]TGATGGAGATGTACT	84182
rs751408100	snp	A/C	2.11062e-05	0.00324848	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882394	CCCACCCACCCAACC[A/C]TGTCCCCAAGGAGCC	84182
rs751436398	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30865840	GCTCTCAATCGAAGA[C/T]CCTGTGCCTGCATCG	84182
rs751438977	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30846996	GGCCACAGACCAGTG[C/T]CAGTCTGTGGCCTGG	84182
rs751452190	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30884658	CTCTACCCCTCCCAG[C/G]GGGTGGCCCACCACC	84182
rs751456934	snp	A/C	3.31444e-05	0.00407076	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828769	CCTCTGTGCTGTGCC[A/C]ATCAGGGCCCAAGGG	84182
rs751487634	snp	A/G	1.65616e-05	0.00287759	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778469	CCATGGACCAGGAAC[A/G]CCCACGCTCTGACCT	84182
rs751495240	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30807796	GCCCGCAGTCACGTA[C/T]CCCCTGCTTGCTCAG	84182
rs751497332	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30774360	GGCCCACCCCTCCAT[C/G]TGTGCATGCCCTCTC	84182
rs751544437	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30848673	AGCAGCTGGGGCATC[C/T]GGTTCGGTGAATGCT	84182
rs751584291	snp	A/G	0.000156638	0.0088484	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872195	CTAGCGAGGTTTGCA[A/G]CCTGGGTCAGGCAGA	84182
rs751588376	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30860383	GACCTTATTAAATGC[A/G]TGTGAGTACACAGCG	84182
rs751599098	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30786279	TACCTACTCAGCTTT[A/G]TCTTTGCAGTTCAGG	84182
rs751625394	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30773664	TGCAGTGACTGTGCC[A/G]TCCTCCCTCTGCCAC	84182
rs751635881	in-del	-/T	1.65677e-05	0.00287812	frameshift-variant, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840803	TCCAAGGCTGTGTCC[-/T]ACAGAAACTCCTGTT	84182
rs751648242	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30815925	AAAATGAAGGCAGTG[C/G]CTCAAATATCCAGCA	84182
rs751650457	in-del	-/CAG			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30788738	GTTCCATGAAAAAAC[-/CAG]CAAGTTCACTCGCAG	84182
rs751682278	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30814288	AATCAAATGCTATTC[A/G]GGTTATTATCATTTT	84182
rs751707554	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30864903	GGCAGTGCTCACCCC[A/G]TCAGAGACCCTCTGG	84182
rs751764290	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30881942	GGGGCGAGTGATACC[A/G]GGTCTCAGGTCTGTA	84182
rs751772233	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30843610	CCCACCCCCAGGCCA[A/C]ATCCATGGGGTGGAA	84182
rs751773349	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30816644	TCTGTCCTCACTGGG[C/T]GATCCCTATCTTTGT	84182
rs751782574	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30845020	GTTCAGGGTCACATC[C/T]GGCATCCCTGGCAGA	84182
rs751784278	in-del	-/TCTTCT			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30877661	GACAAAGCCCTTCCC[-/TCTTCT]TCTTCTTCTTCTTCT	84182
rs751792153	in-del	-/A	1.6562e-05	0.00287763	frameshift-variant, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785874	TGCATGGGAGAAGAT[-/A]AGACAAGCTTCACTC	84182
rs751848764	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30804006	AAATCCCATTCAGTC[C/G]TGCTGGAGTACTGGG	84182
rs751857374	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30854474	GTGGCCTGAACTAAG[G/T]CCAGCAGACCCGCGA	84182
rs751890420	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30805045	AGGCAATAGAGAGGG[A/T]TAGAAAGTTCTCTTG	84182
rs751914125	in-del	-/CA			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30831853	GTATCCTACAAAAAG[-/CA]CATAAAATAGTATGG	84182
rs751920519	in-del	-/ACACACACA			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785290	CACACACACACACAC[-/ACACACACA]CACCCATTGGCACAC	84182
rs751922948	snp	A/G	1.65679e-05	0.00287814	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778579	TAAGGTGTGGTGTGG[A/G]GTCTTGGAACTGAGT	84182
rs751923154	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30826562	GTGTGATGGCCCAGA[C/G]TGAGACGAGGCTGGG	84182
rs751933539	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30834268	ATCTAGGCGGAGGTT[C/G]CCAAACCTCAATTCT	84182
rs751940757	snp	C/T	1.73429e-05	0.00294468	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882172	ACATCAGGCCTCTCC[C/T]TCATCCAGGTTGGCT	84182
rs751960716	snp	G/T	1.85228e-05	0.0030432	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853411	TACGCTTCACAGTTT[G/T]ACCTGCTATGAGGAC	84182
rs751975881	in-del	-/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30789287	CTTGGACCTGCTTCA[-/C]TGCCAAGGGCATTGC	84182
rs751977891	snp	A/G	1.65927e-05	0.00288029	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782002	ATCCTCTAAAAACAA[A/G]CCTTGAACTCATCAC	84182
rs751993032	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30861451	AGGCTGAGGGAGGTG[A/T]GTAGGCTTCAAGATT	84182
rs752033088	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30844659	AGAGGCTACAGAAGG[A/T]TGTCCTTGCCAAGTG	84182
rs752068731	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30825290	TCTATGTGGAAGCAT[A/G]ATTGAAGTCTCCTCT	84182
rs752085470	snp	C/T	2.1679e-05	0.00329227	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850483	CAGATGCCCACCGGA[C/T]CCGCTGCCTCGTCCT	84182
rs752104626	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30888728	TTAAAATGTCTCTGC[G/T]TTGATTTTCTATTGT	84182
rs752116116	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853199	CCTGACGACTCCAGC[A/G]GTACCGGCCAGCCTT	84182
rs752136757	snp	C/T	1.72172e-05	0.00293399	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839160	TCGTATTGTTGCTTG[C/T]TTTTAAAACAACCAG	84182
rs752153102	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852958	TGAAAAAGCAAAGGA[A/G]ACTCCTAAGGGCTGC	84182
rs752255691	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30803155	TTCACTGTACCTATA[C/T]TTGGACATGATCTGT	84182
rs752305191	snp	C/T	1.65636e-05	0.00287776	utr-variant-3-prime, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30892034	GTAAACCCTGTGGTC[C/T]ACCACTCATCACCTC	84182
rs752307525	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30777820	AAGCCAGGCACTTGC[G/T]AACAGGACCCTCACT	84182
rs752347303	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30854488	GGCCAGCAGACCCGC[C/G]ACCTCTGAGACCCCC	84182
rs752357100	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778683	TGCGGTCAGAGAGAA[A/T]CGGACCCCCCAAATG	84182
rs752372079	snp	C/T	1.65798e-05	0.00287917	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836745	CAGCATCAAAACCAA[C/T]TGACCTCTCAGTAGC	84182
rs752372146	snp	A/G	1.65553e-05	0.00287705	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853500	GGATGTGCGTCACTA[A/G]GCCTTCTGATTTCAC	84182
rs752387554	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30884767	TCCCAGCGTGGGCCC[A/G]GGATTGGACTTCTTG	84182
rs752417532	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30868694	TGTTCTGTTTCTTGA[C/T]ACAGCGTAGTATCTC	84182
rs752443505	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30885901	TCCACTTCCCCCATC[A/G]ATCCCCCATCATGGT	84182
rs752446915	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30780894	TATTGTAAGCTTCAT[G/T]TAATCTTAGACAAAA	84182
rs752495036	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30862943	GTGAAGCAGATGCAG[C/T]GGAATGACTTTGATT	84182
rs752503699	snp	A/G	0.000263644	0.0114783	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791599	CTATGCAAAGGTGAC[A/G]GCTTTTCAAAAAGAA	84182
rs752568970	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30863915	TGGCTAGAACTTTCC[C/T]CAGGGAGCTCTCACA	84182
rs752583091	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30884766	CTCCCAGCGTGGGCC[C/G]AGGATTGGACTTCTT	84182
rs752584448	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30827780	ACGCCCCTTCATACA[C/T]CTTCAGGAGGAAACC	84182
rs752585337	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30874032	GATTTATTAACCCCC[A/G]ATGTCATTTTAACGA	84182
rs752604478	snp	A/C	4.97047e-05	0.00498496	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852193	CCACTCAGAGGACTC[A/C]TGCACCTTCCTTTCC	84182
rs752655597	snp	C/T	2.89272e-05	0.003803	missense, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771522	TCGTGGAGGAGGTGG[C/T]CGCCTCCTTGGTCAG	84182
rs752660161	in-del	-/A			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30809378	GAAGTATCCTAAGGA[-/A]AAAAAAAAAAAAAAA	84182
rs752691481	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30865704	TAGGCCTTTGTTGTC[C/T]TGTGGCAACCCAAGG	84182
rs752713697	snp	A/G	1.65603e-05	0.00287747	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875459	TCAGTAACTGATTCA[A/G]ACTTGATGAGTCTTT	84182
rs752723286	snp	A/G	6.63911e-05	0.00576118	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785751	TCCTTTTTCACAGAC[A/G]TGACAATCTTGATGG	84182
rs752761273	snp	G/T	6.62658e-05	0.00575574	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859272	TTTGAAGTGGGCCCC[G/T]ATGGCTGCATCCTGC	84182
rs752762047	snp	A/G	2.58154e-05	0.00359264	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859182	GCTCCCTGGGGTGTG[A/G]CTCCCACAGAGGTGT	84182
rs752768388	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30818001	TATTGGGTATGTGTG[G/T]GATGCTGGACATCCT	84182
rs752777915	snp	A/G			synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882195	GGTTGGCTGCTTCCT[A/G]AAGACCCCGAGGTTC	84182
rs752782991	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30816915	ATATGTTGTAGGTCA[A/G]CCGTTTGAGAACTGG	84182
rs752785536	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30803261	GCTGCCTGAGTATAG[A/G]GGTGACTTGTCTGTG	84182
rs752794377	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30808920	GAGACAGAGAGACAA[A/C]GAGGGAGTCAAGGAG	84182
rs752802860	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30775679	TCTGGTGACCAGCCC[C/T]CATCCTGAAGCTATC	84182
rs752841130	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30780834	TTACTGAGAGAAAAA[G/T]CAAGAAGGCTACAAT	84182
rs752842737	in-del	-/A	1.65707e-05	0.00287838	frameshift-variant, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782019	CTTGAACTCATCACC[-/A]GATACTTTCTGGATC	84182
rs752851318	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872113	GGCACAGAACAGAGC[A/G]CTCAGGTTCCCACCA	84182
rs752852374	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30788327	ACTTTTTGTACCTTA[C/T]CAGTTTCGCTTGATA	84182
rs752871886	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30858500	CCGGGACACCAGCTC[C/T]AAACCAGAGTTGGGA	84182
rs752876461	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30832902	ACCCCTTATACTCTT[A/G]TTACCTTCCTTTCCC	84182
rs752878324	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30855381	TTGTGAGAGTGCAGC[A/G]GTCACAGGAGAGGCG	84182
rs752879480	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30843685	GCAAAAGCCATCCAG[A/G]TTGGGATCCCAAGGG	84182
rs752908229	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30806671	CTGGGGTCAGGCATA[C/T]AGCAGGCTTTTGGAA	84182
rs752928003	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30881346	CTTCCACAAACACTT[C/T]CACCATGTGAAATTC	84182
rs752945933	in-del	-/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30846073	AGGAAGTCCTCCTCT[-/C]ACTTCCACTTCCCCT	84182
rs752988147	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30812517	AAAGAAGTGGAACCA[A/G]GTTTGTTATTCAATG	84182
rs753004592	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30825360	GCTGGGCTCTTGTGC[G/T]GATGGATGGCCCTCT	84182
rs753047153	snp	C/T	3.39144e-05	0.00411777	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840865	TAAGTCAGTGCTCTT[C/T]CTGGCAATATCTTAT	84182
rs753048755	snp	A/G	1.6577e-05	0.00287893	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791366	AAAACCACTGCCAGC[A/G]GCCCTCCCCATCTGC	84182
rs753087784	in-del	-/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30824774	GAGAGGGTCTTGATA[-/C]TGTTGCCCAGGCTGG	84182
rs753107804	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30861544	TTTTGGGTTTGCTGT[C/T]TGAAAACCTGAACTT	84182
rs753120560	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836062	GTTACTTAACTCCTC[C/T]AAGCCTCAGTTTCCT	84182
rs753120620	in-del	-/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30824738	GACACCACGCTCAAC[-/T]AATTTATTTATTTTT	84182
rs753142744	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30851827	ACCCAGGGGGAGCCT[C/T]GGAGAGGATGGAGGT	84182
rs753168544	snp	A/G	1.65608e-05	0.00287752	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778489	CGCTCTGACCTCAGC[A/G]TAAACAACAGAAATG	84182
rs753172535	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30860248	AGACACTTCTTTCCC[A/G]GCCTGGTTGGGTCTG	84182
rs753185822	in-del	-/TCATTCTT	1.66192e-05	0.00288259	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840747	CTGGCAGCAATGGTC[-/TCATTCTT]TGCAGGGTGGTCCTT	84182
rs753218945	in-del	-/CTT			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852575	AGGCTTCCCTGTGTC[-/CTT]CTTCCTCTTTCTTTA	84182
rs753257825	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30798150	ACACACCTGGACAGC[A/G]TGTTGCCGTATTGAA	84182
rs753270802	snp	C/G	1.66109e-05	0.00288187	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859363	CCCTGGGGCTGGGCT[C/G]GTCTGTCTTGTTCAC	84182
rs753281899	snp	A/C	1.65696e-05	0.00287828	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840789	AGTCCTGGCAGCTGT[A/C]CAAGGCTGTGTCCTA	84182
rs753285061	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30813392	CTTGTGCTCCCGTGC[C/T]GTGGGGTTCATGGAA	84182
rs753289582	snp	C/T	5.64371e-05	0.00531182	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853398	TGTCTTCTCAGCTTA[C/T]GCTTCACAGTTTGAC	84182
rs753310221	in-del	-/TT			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785294	ACACACACACACACA[-/TT]CACACACCCATTGGC	84182
rs753313166	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30803508	ATTGAGATGCCGTAG[C/G]AGCTTAGAGGAGAGG	84182
rs753348251	snp	C/G	1.66824e-05	0.00288806	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30781983	CAATGATAGGCAAAG[C/G]AAAATCCTCTAAAAA	84182
rs753353490	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30832977	GTATGTTCTTGCAAA[A/G]TCTATACTGTTTTGT	84182
rs753415780	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30790664	TGGCAAGGCTGGTCT[C/T]GAATTCCTGACCTAA	84182
rs753423346	in-del	-/ACACACACACA			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785288	CACACACACACACAC[-/ACACACACACA]CACCCATTGGCACAC	84182
rs753436122	snp	A/G	1.65773e-05	0.00287895	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882962	ACAGACAACGACCTT[A/G]TCCCACCCCTCGAGC	84182
rs753446940	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30858454	ATAGCAAGGAGTGGC[A/G]GAGCGAGGATTTAAA	84182
rs753472788	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30809147	GTTCTCCATAACCCT[A/G]TAACACTCCAGTACC	84182
rs753519433	snp	A/G	1.68459e-05	0.00290219	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872290	ACCTGATTGGAGCAC[A/G]TGGCTACTGTACACA	84182
rs753540044	snp	A/G	1.66576e-05	0.00288592	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30786022	CTTTCTGTTGTTATG[A/G]GACTGGAGGCTGAGA	84182
rs753540132	in-del	-/GA			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30805502	CAGTATCTTGCAGTG[-/GA]GACCACGTGCTTGGT	84182
rs753546186	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836407	TAGCTAAGTCTCACT[C/T]GGCAACATCCTCGTG	84182
rs753555573	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839028	TGAGTTTCTCTTTCA[C/T]CAAATATAAGAAGAA	84182
rs753565965	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30824054	ATCAAATATATAGCA[A/G]ATGTCTTAGTCTGTT	84182
rs753577859	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859404	CTAGAGCCCAGGATG[A/G]TGCTTGGCACATGTT	84182
rs753605264	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828902	CTCTCTGATTGATGT[C/G]TTCTACTGCTTGCCC	84182
rs753635189	snp	C/G/T	0.000101419	0.00712047	utr-variant-5-prime, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771457	CCTGGTGCTGCGGCC[C/G/T]GGCGTGGGCCTCGTG	84182
rs753645859	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30849418	CTAGAAGTACACCTC[A/G]AAGGAGTCCTGGGAA	84182
rs753655658	in-del	-/T	5.27468e-05	0.00513523	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850584	AGGTCTGTGTTGCCG[-/T]GGCTCATCGTCTGCT	84182
rs753682617	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30774676	TAGTCCTCGCCCTTC[C/T]TGATCTAATGATTAT	84182
rs753684063	snp	A/T			synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875599	ACTTCTCAGAGGCAT[A/T]GCTGCACGCAGTGAT	84182
rs753687417	snp	A/G	2.91822e-05	0.00381972	missense, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771496	CAGAGCCAGAGCCAT[A/G]GACAGCCTCTTCGTG	84182
rs753701081	snp	C/T	1.69387e-05	0.00291016	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836815	TGATTTGAATGGATA[C/T]AGATGGCGTGATTTT	84182
rs753705446	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30797849	GGTGGTGGCTTGCAT[C/G]AGGGAAATGGCAGTG	84182
rs753726529	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30835215	CACATGGCTGGGGAG[A/G]CCTCACAATCATGGC	84182
rs753732609	snp	A/T	1.65608e-05	0.00287752	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875454	CTCTTTCAGTAACTG[A/T]TTCAGACTTGATGAG	84182
rs753733656	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30860716	CGCCTTGTTACATGC[A/G]TGCTCCTGCATGTAG	84182
rs753736971	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30837902	TTTCTCCTGTGTGCC[A/G]CCAGCCCACATTTGA	84182
rs753795286	snp	C/T	1.65603e-05	0.00287747	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785949	CAAAGTCTGGTCTGA[C/T]TGTGCGAGGCATGAT	84182
rs753829737	in-del	-/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30884381	TGCTGGTGCTTCTTT[-/C]GTCGGGAGGATTAAG	84182
rs753838708	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30848435	TCAGGATGTGCAGTT[A/G]ACAGTACATGGCCAT	84182
rs753845558	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30794710	GTCACCTGGACTCCC[A/T]TTGTGGGGGTTGTGG	84182
rs753849095	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30814920	TACGCAGGGGAATGC[C/G]TTATAAGTTTGAAAG	84182
rs753855580	snp	C/T	1.65616e-05	0.00287759	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30891947	GTCTCTCTCCTCACT[C/T]TACGCTTAGGTGGAA	84182
rs753870329	snp	C/T	1.78662e-05	0.00298878	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791580	CACCTGTCAGGTGAG[C/T]GTGCTATGCAAAGGT	84182
rs753872375	in-del	-/CCCATGT			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30838954	TTACAAAGATTTTGG[-/CCCATGT]CAGCACAGGCTAGCT	84182
rs753932019	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30830541	GTCCTTCTTCACATG[A/G]TGGCAGGAAGGAGAA	84182
rs753936412	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30835378	AAAGACCCACTCCCA[C/T]GATTCGGTTATCTCT	84182
rs753957973	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30774214	TCCCCATCTAATTTC[A/G]CTGAGAAAACAGAAG	84182
rs753977753	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30890193	GCATCCACCTGTTTC[A/G]ACCTTTTATGCCGAG	84182
rs753998660	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872193	ACCTAGCGAGGTTTG[C/T]AACCTGGGTCAGGCA	84182
rs754009821	snp	C/T	1.75443e-05	0.00296173	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882330	CTACGATGGCCTGGC[C/T]AACCAGCAGGAGCAG	84182
rs754144405	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872854	AAGGGACCTTTTCAA[A/G]ATGTTACCTAGTGAG	84182
rs754145904	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30801824	TGAGATCCAGAAAGT[A/G]CGGCTAAAGAAGTGA	84182
rs754161745	snp	A/G	3.36208e-05	0.00409991	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839309	AATACGGCATAGTGC[A/G]GAACAAGGCAGGTTG	84182
rs754187410	snp	A/G	1.6571e-05	0.0028784	splice-acceptor-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859255	TTCTCTCCCCCTCCC[A/G]GTTTGAAGTGGGCCC	84182
rs754189113	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30783775	TTAAATTCCATGATC[A/G]TAAGGTTCAAGCACT	84182
rs754198097	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785344	GCTGAACAGTGGGGA[A/G]TGCCAAGTTTGCTAT	84182
rs754208139	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30808891	GGAAAGACCAACAGA[A/G]AGAGAAAGAGGAAGA	84182
rs754215448	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30851885	GGCAAGTCAGCATTC[C/T]GCAGTCTGGAAACAC	84182
rs754219328	in-del	-/T	3.39055e-05	0.00411723	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30781971	TTTTTTCTCTCCCAA[-/T]GATAGGCAAAGGAAA	84182
rs754234632	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30841138	AGACGGCAAGCTGCC[C/T]GAATCCCTTCCACCC	84182
rs754269021	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30813588	GAGGAATGGGACCCA[C/T]GGTTTGCTACCCAAG	84182
rs754286918	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30879999	CAGTGGAAATGTGTG[A/G]GTTTGATTATTTAAT	84182
rs754298334	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30842200	CAATGTAACACTTCC[A/G]TGGCAAGATCTCACC	84182
rs754298984	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30878990	CTTTCCCCCTTTCCA[A/T]TCCTGTCCCTTCACT	84182
rs754310287	in-del	-/CCATCTTGC			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30886177	CCCACAGCATCTTGT[-/CCATCTTGC]CCATCTTGCTCGGTA	84182
rs754316959	snp	A/G	8.39906e-05	0.00647983	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785714	CTGATTCCTTTTGGG[A/G]AGTCTGTTTTAATGG	84182
rs754374573	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30879195	AGAAAGGGCCTTTAA[G/T]GAAATGATTAAGGTA	84182
rs754396293	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30788043	ACAAAAAATTAGTGA[C/G]ATGAGTAGCATTTTT	84182
rs754417879	snp	C/G	0.000132562	0.00814024	stop-gained, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836736	AGTTGCAGACAGCAT[C/G]AAAACCAATTGACCT	84182
rs754451744	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30801551	CATTTTACCCTATAC[A/G]TGTGCCCCCAGTCCA	84182
rs754470539	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840451	ACACAGAAACATTTC[C/G]CTAGATGATAGAAAA	84182
rs754483810	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30878042	CCCTCGGGCCCTACA[C/T]AGTTAGCCACATTGG	84182
rs754536735	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30789435	TTTGAGTACCTTGGC[C/T]GTACTTATTGGTTGC	84182
rs754553425	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30876829	CCTATCCTCAGAACC[A/G]GGACGCAGAGATTGA	84182
rs754582983	snp	A/G	1.66051e-05	0.00288137	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852328	TGGCTTTGTTTGGGG[A/G]CTGTCTCCTTTCATA	84182
rs754583305	in-del	-/GCAGGCAAAGAGAGCTTGT			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30835272	CTTATGTGGATGGCA[-/GCAGGCAAAGAGAGCTTGT]GCAGGCAAACTCCTG	84182
rs754674153	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30818530	GAAGAATAAAGAATA[G/T]ATGAAGAATCTGAAG	84182
rs754685088	snp	A/G	7.50413e-05	0.00612495	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853399	GTCTTCTCAGCTTAC[A/G]CTTCACAGTTTGACC	84182
rs754711606	in-del	-/C	8.59587e-05	0.0065553	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859119	TCAGCCTTCGGGCCA[-/C]CCAGCAACCCCAGGG	84182
rs754729522	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30855689	GTACCCCAGGGCTTT[G/T]ATGAAGCCTAACCAA	84182
rs754735794	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30815434	GCTGTGGGCCAGGCA[A/C]CCCATCACATCTCTA	84182
rs754739957	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30884701	ACTGCCTCTTCTGGA[A/G]TAACTCCTTTTTCTC	84182
rs754759860	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872394	CCTCCTCTTGCCCCA[A/G]AAAAAGACAAGTCTT	84182
rs754806093	snp	A/G	1.70793e-05	0.00292222	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872223	AGAGCTGTGCTAACA[A/G]TGCTTCTTGTGTTTT	84182
rs754812917	snp	A/G	2.90846e-05	0.00381332	missense, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771497	AGAGCCAGAGCCATG[A/G]ACAGCCTCTTCGTGG	84182
rs754826617	snp	A/T	1.65603e-05	0.00287747	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785950	AAAGTCTGGTCTGAT[A/T]GTGCGAGGCATGATG	84182
rs754852371	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836417	TCACTCGGCAACATC[C/T]TCGTGGTATGAACAG	84182
rs754887052	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30796015	TCCCCCCTTGCCATG[C/T]AACCGAACACATTCA	84182
rs754895512	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30837015	TCCCCTCCAAATACC[A/G]TGGGAATAGAGCTGC	84182
rs754917488	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30845361	GCAGGAACCTCTCTC[A/G]GTCCTCAGCTCCTCG	84182
rs754949629	snp	C/T	3.33979e-05	0.0040863	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30786032	TTATGGGACTGGAGG[C/T]TGAGAACTGGGCTGG	84182
rs754978057	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30807832	CACGACCCTCTCACG[C/T]GGACTCTGTTAGAAT	84182
rs754998546	snp	C/T	1.69066e-05	0.00290741	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872298	GGAGCACATGGCTAC[C/T]GTACACAGGTCAGGG	84182
rs755019960	in-del	-/CT	0.000340715	0.0130477	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875698	AGTAGGGGAGCCTGA[-/CT]CTCTGGAGCAATGAG	84182
rs755030505	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30873022	GACGGGCTGGACAGA[C/G]CTGCACATCTTCTGG	84182
rs755059308	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30854487	AGGCCAGCAGACCCG[C/T]GACCTCTGAGACCCC	84182
rs755059407	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30842525	CCACCTTCCTTCCTT[A/G]CACTGAAAAAAATGT	84182
rs755061779	snp	A/G	3.70069e-05	0.0043014	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882340	CTGGCCAACCAGCAG[A/G]AGCAGATCCGGCTGA	84182
rs755140213	snp	A/G	0.00026996	0.011615	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791539	GAGGCTGGAAAGAGC[A/G]TTCAAACGGCAGGGC	84182
rs755158819	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30833701	AGGCAAGTCCCTTCC[A/G]CCTATTAGCCAGTAA	84182
rs755164658	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859768	AAGGCTGGCATCCTG[C/G]GTGGTGAATGGGCGG	84182
rs755168309	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30805117	CAAGGTGAGTCTAGG[G/T]GTGCAGCAGGTCTGA	84182
rs755198841	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30856534	TTGGGGTTTACAGTG[A/G]GTTTCTGTGTCTGTT	84182
rs755207566	in-del	-/TTTTGTCCTTACTCCCTT	1.8249e-05	0.00302062	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791144	AAGGGTCCTCACTGC[-/TTTTGTCCTTACTCCCTT]TAGGATTCTTTTCAC	84182
rs755211260	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30834279	GGTTCCCAAACCTCA[A/G]TTCTTGACTTCTGTG	84182
rs755211314	snp	A/T	6.62603e-05	0.0057555	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782061	ACGGCTAACAATTTC[A/T]CTCAAGATACCCCAA	84182
rs755220381	snp	C/T	8.30862e-05	0.00644486	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882266	TCTTTAGCCTGCAGC[C/T]GGGGCTCCTGCGTGA	84182
rs755254717	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30870597	TCCGTGTTTGGCCAT[A/G]GTTATTAAAAACCAC	84182
rs755309846	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30889822	AAAGTGTTATCATAT[A/G]CCTCTTGTCACAGGT	84182
rs755342881	snp	C/T	1.65737e-05	0.00287864	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778407	ATTTAAGATGGTAAA[C/T]AGCGATTCAGCTTTC	84182
rs755345653	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30781392	AATACTGGTATCGTT[G/T]AATTCCAAAACCTAC	84182
rs755362610	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30871300	GGTTGCAATTGCCAC[C/G]TGCTGAGCACAGTGA	84182
rs755386534	snp	A/G	6.62998e-05	0.00575721	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840772	CAGGGTGGTCCTTGC[A/G]GAGTCCTGGCAGCTG	84182
rs755413231	in-del	-/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30817833	CTCATTCATTATAAT[-/C]TAACCCTCTTGTTCA	84182
rs755417188	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30841187	CCTTTCGACTGCGTC[C/T]GGGCCTCCCTTCCCT	84182
rs755460085	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30793682	CATCGTGGGCCCAGG[A/G]CAGGTATTCTCATAT	84182
rs755465755	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30825294	TGTGGAAGCATAATT[G/T]AAGTCTCCTCTGGTG	84182
rs755501587	snp	C/G	0.000304409	0.0123334	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859172	AGGGCAGGCTGCTCC[C/G]TGGGGTGTGGCTCCC	84182
rs755505473	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30811298	TTTAAAACTCTTGTA[A/G]TAGGAGTTATAATAG	84182
rs755574717	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30777821	AGCCAGGCACTTGCG[A/G]ACAGGACCCTCACTT	84182
rs755579208	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30796008	ACCTTAATCCCCCCT[C/T]GCCATGTAACCGAAC	84182
rs755589582	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30856890	ATCAGCATTACTCTT[G/T]GCCATTGTCAGAGCA	84182
rs755626172	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30890095	CACTGAACATCACCA[A/G]ATGACACGGAGGAGG	84182
rs755651493	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30822035	TATTTATATATACAC[A/G]TATTTTTCTGATGAT	84182
rs755652998	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30866290	AGAGAAAGAGGACAG[A/G]CCTCAGAAGGAGGGA	84182
rs755693382	snp	A/G	1.65614e-05	0.00287757	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875579	TCTGGGGATGGGAAC[A/G]TCACACTTCTCAGAG	84182
rs755694095	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30832072	AACCAACTCCCTGCA[C/T]TTGGGCCAATTCCTC	84182
rs755694405	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30848995	ATCTCCTTTAAAGCC[A/C]CGAGGGAGGTGCAGT	84182
rs755696512	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30847071	TGATGCTTTGGGGGC[A/G]TCTGACCCAGTGTCT	84182
rs755701876	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30821142	CTCCTGTTTATTATG[C/T]CTGGTGTTTTAGTTT	84182
rs755729640	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30818704	ACATCAGTAAAACTC[C/T]TCGTGTATATGTTGG	84182
rs755777043	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30774581	TTTCTCTGCTTTCTC[A/G]AACCCATTTTAATCA	84182
rs755816009	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30884852	GGAGCTTAGTCCATG[C/T]AGAGTGAGAGTCTTA	84182
rs755822036	snp	A/G	1.6773e-05	0.0028959	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875646	TCTTTGAGCATTACA[A/G]CATGTGCCAGGTACC	84182
rs755850594	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30820878	AATGGAATTGCAGAA[A/T]AATGCTATTTTTAAC	84182
rs755852563	snp	C/T	1.65652e-05	0.0028779	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852221	TCCTTTTTAGGGCTT[C/T]GAGAACACAGCAGTT	84182
rs755862424	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30846296	CGTCACAGTGGACAG[A/G]TGAGGCTATTTTGAG	84182
rs755877740	snp	A/G	1.72095e-05	0.00293333	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872216	GTCAGGCAGAGCTGT[A/G]CTAACAATGCTTCTT	84182
rs755908286	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30835209	AAATTGCACATGGCT[A/G]GGGAGGCCTCACAAT	84182
rs755944085	snp	A/G/T	0.000100273	0.00708008	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882880	TCAGGGTGAGTGCAG[A/G/T]GCCCTGGGTGACATG	84182
rs755954323	snp	C/T	1.65784e-05	0.00287905	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828788	AGGGCCCAAGGGGTC[C/T]TCGTTGGCTCTGTCT	84182
rs755964114	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850699	CTGCAAGCCAGCCTG[A/C]TGTGCTGAGCAGCCG	84182
rs755971007	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30864944	GGGGGTGGGTGGTTC[A/G]TGGGGTGAGATGTGA	84182
rs755983291	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30881789	ATTTGTTTGAGGGGT[A/G]TGGGAAGAATTGGTT	84182
rs756013836	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836582	AACTTAGCAATGTCT[A/G]TGGTGTTCAGTGACT	84182
rs756022789	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30858695	ACATGCATCTACATG[A/G]CTGCCTCCTTCGCCT	84182
rs756024685	snp	C/T	3.40478e-05	0.00412586	utr-variant-5-prime, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771449	CCCAGTTGCCTGGTG[C/T]TGCGGCCCGGCGTGG	84182
rs756028393	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30808877	GCTGGCAGAGTCAAG[G/T]AAAGACCAACAGAGA	84182
rs756029503	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785669	CTTGCTTTGAATGCA[C/T]ATTGAATGTGGAATT	84182
rs756055480	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30837790	CCCAGGGCACGTGGC[C/G]TCTGGAAAGCAGAGT	84182
rs756091871	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30871630	GGACTCCATTCTGAG[G/T]GTGGAACCACAGTGG	84182
rs756142811	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30879845	TTAAGATGCAAACTT[G/T]CCCACATTTGAGCAC	84182
rs756178537	snp	A/G	3.34236e-05	0.00408787	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791521	TTCCAGGATGACCCA[A/G]GAGAGGCTGGAAAGA	84182
rs756182284	in-del	-/CCAAAGTCTTAACT			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30833622	CTTCCCAACAGTCCC[-/CCAAAGTCTTAACT]CATTTCAGCATTAAC	84182
rs756210791	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30775704	GCTATCTAGGGGTCC[C/G]CATCCACTAGTCATC	84182
rs756219513	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30834421	GATGTAGGGCACCAA[C/G]TCCTTATGCTGTACA	84182
rs756260993	snp	C/T	3.31296e-05	0.00406985	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782047	ATCACTTTGGAAATA[C/T]GGCTAACAATTTCAC	84182
rs756297094	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30861595	TAGGCCTGACTCTCT[A/T]CTCCTCTGAATAGAG	84182
rs756302522	snp	A/G	3.31768e-05	0.00407275	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791467	CGGCAGCACAGACAC[A/G]GACAGGATGCCCTTG	84182
rs756305355	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30793172	TAATTGTTTATATAT[A/G]TATTATTCTTTATGA	84182
rs756305409	snp	C/G			upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30770180	GCTACTCAGGAGGCT[C/G]AGGGAGGAGAATGGT	84182
rs756308233	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30794510	CTAGGGGCACAGGTG[A/G]GGTTAGGGGGCAGGT	84182
rs756327379	in-del	-/C	2.19575e-05	0.00331335	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882405	ACCCTGTCCCCAAGG[-/C]AGCCTCCAGGCTGGT	84182
rs756395735	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30825407	ACCAGAGAGAGAGGC[C/G]AAGCTGTACCCTACC	84182
rs756400824	snp	C/T	1.66746e-05	0.00288739	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839216	AAATAAAGACCCTTC[C/T]GTTTGGTTCCAGCTT	84182
rs756426759	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872127	CGCTCAGGTTCCCAC[A/C]AAATCTGGAATTCTG	84182
rs756467424	snp	A/G	0.000175323	0.00936114	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859164	GTTGGCTCAGGGCAG[A/G]CTGCTCCCTGGGGTG	84182
rs756491635	snp	C/G			upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30770740	CGGGGAAAATGTACT[C/G]GGCTTGGTTAGAAAC	84182
rs756508610	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30888916	GTTGTCTAGTGGTAG[A/G]TGAGTGTGACTCACC	84182
rs756521064	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30801688	TCCAAAAATGGGGTT[C/G]ATGACCCCTAAACCT	84182
rs756538445	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30876891	ATTCCACCCTGGATT[A/T]TCAGGGTGGAAAAAG	84182
rs756541229	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30781144	CAGAGTGCCCCATGT[A/C]CAGCCACGGCTCGGC	84182
rs756547396	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30812530	CAGGTTTGTTATTCA[A/G]TGCTGGAATCTGGGT	84182
rs756562102	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30830947	TGAAATGAAGACTGG[A/G]CTGGGCAAGATGATT	84182
rs756564521	in-del	-/CTGG			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30888448	AGACCCGGCTATAAA[-/CTGG]CTGGCTGGCTGTCAG	84182
rs756571875	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30783034	TAGCCTAGCCACATT[C/T]TTAATCCTCACAGTA	84182
rs756580010	snp	A/C	1.98714e-05	0.00315203	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853445	GTGACTTTTCTTCAA[A/C]AAAGCATTCATCAGG	84182
rs756618501	snp	A/G	1.66123e-05	0.00288199	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882261	CATCCTCTTTAGCCT[A/G]CAGCCGGGGCTCCTG	84182
rs756696540	snp	C/G	1.656e-05	0.00287745	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875555	TTCAACGATGTGGTT[C/G]AGCTGGATTCTGGGG	84182
rs756703789	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30779969	TAAAGGATGGAATTT[C/T]AGGCAAACATATAAA	84182
rs756715663	in-del	-/CATCAGTGAACTGGAACGGCT	1.656e-05	0.00287745	cds-indel, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30891968	TTAGGTGGAAGGGGG[-/CATCAGTGAACTGGAACGGCT]CAGACCCCATCCTGT	84182
rs756728654	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30878141	CTGGCCTGGCCTGGC[C/T]CTCTCCTCAGGCAGC	84182
rs756756551	snp	A/G	1.65839e-05	0.00287953	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778384	CTTTATGAGAACAGC[A/G]GGTTTTGATTTAAGA	84182
rs756760402	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778748	TCGGTCAGCTGGTGC[C/T]GCCCATTGGCGTGTT	84182
rs756806488	snp	C/T	0.000104772	0.00723707	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850582	CGAGGTCTGTGTTGC[C/T]GTGGCTCATCGTCTG	84182
rs756838754	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30822364	TTAGTAGAGACAGGG[A/T]TTTGCCATGTTGCCC	84182
rs756854167	snp	C/T	1.81394e-05	0.00301154	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791149	TCCTCACTGCTTTTG[C/T]CCTTACTCCCTTTAG	84182
rs756894148	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30783336	AAGAAGGACCCCTGT[A/G]ATTACATTGGGCCCA	84182
rs756908470	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30797884	TGGTGAGACATGGGC[C/T]AGAATATGGGTGTAT	84182
rs756942795	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30837216	CCACTTAAAGGGCCC[C/T]GTGGTCACAGGGGAC	84182
rs757004113	snp	G/T	3.31208e-05	0.00406931	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875483	AGTCTTTCCCCTTTC[G/T]CTCATCTGCAGGAAC	84182
rs757031817	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30864088	GAAAACCTTTTCATG[C/G]AGTAGATTCTTGGCC	84182
rs757043983	snp	C/T	6.62405e-05	0.00575464	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785829	GTAAGCCCATGCAGA[C/T]GGTCCCGGGTGAAAC	84182
rs757061997	snp	C/T	1.65831e-05	0.00287945	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785761	CAGACATGACAATCT[C/T]GATGGAGATGTACTT	84182
rs757092029	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30786930	CAAACTCAAAGTGCC[A/G]TATCAGTCAAATCAG	84182
rs757114326	snp	A/G/T	4.97165e-05	0.0049856	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828770	CTCTGTGCTGTGCCC[A/G/T]TCAGGGCCCAAGGGG	84182
rs757116104	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30816980	TTGCTACACATTGTG[A/T]TAGTTAGTGCACGCG	84182
rs757134631	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30877908	TGGTCTTGAACTCCT[C/G]ACCTCAAGTGATCCA	84182
rs757145172	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30847355	TCAAAGGGGCTGTAA[A/G]CAGAGCCTGTAGGAT	84182
rs757182104	snp	C/T	1.65608e-05	0.00287752	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785823	ACAAAAGTAAGCCCA[C/T]GCAGACGGTCCCGGG	84182
rs757182197	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30799110	TTGCAGGTTGCAGTC[G/T]GCTGAGCAGACCTCC	84182
rs757192915	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30843699	GGTTGGGATCCCAAG[G/T]GGGTGTCTGGGTAGA	84182
rs757204062	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30816096	TAGCCTTTTCAGCCC[A/T]TCCAGCTGGATGAGC	84182
rs757222997	in-del	-/TG			frameshift-variant, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840841	GATAGCAAAGCCGAC[-/TG]TGCTCAGTAAGTCAG	84182
rs757239475	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30829749	GTACAGCATGGAGTC[A/G]GGAGGTGCTGGCATC	84182
rs757240310	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30783101	GAGGTCTGAAGTGTA[A/C]AATCAGTCTCACTAG	84182
rs757273354	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30845156	CTGAGTTTTAGACTT[C/T]CATCGCTGGACACCC	84182
rs757349022	in-del	-/A			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30809798	AAAAAAAAAAGGGGG[-/A]AAAAAAAAGGGGGGC	84182
rs757434900	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872235	ACAATGCTTCTTGTG[C/T]TTTCCAGCATCCGCC	84182
rs757459987	in-del	-/CTTTT	2.80595e-05	0.00374553	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850438	GGCATAAATGCCTTC[-/CTTTT]CTTGTCCGCAGGGGA	84182
rs757478545	snp	A/G	1.65677e-05	0.00287812	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840799	GCTGTCCAAGGCTGT[A/G]TCCTACAGAAACTCC	84182
rs757482605	in-del	-/TG			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30889743	CAATGGAGTAAGTGA[-/TG]TGATGCTGGCATTTT	84182
rs757488712	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30851068	ATCCTGACCCGCATC[A/G]TCTCTTCACCGCTGG	84182
rs757501517	snp	C/T			upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30769914	ATAAATTGTAAAACA[C/T]GTATGTGGATTTAAA	84182
rs757507002	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30879232	GGTCACTAGGGTGGG[G/T]CCCAATCCAGTATGG	84182
rs757525095	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30890202	TGTTTCAACCTTTTA[C/T]GCCGAGTGTTTTAAC	84182
rs757535211	snp	C/T	1.74178e-05	0.00295103	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872198	GCGAGGTTTGCAACC[C/T]GGGTCAGGCAGAGCT	84182
rs757581967	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30841402	TACAGGGGAGAATTA[C/G]ATGAGTTCTGTCCTC	84182
rs757606200	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30789788	TTAAACCAAGGAAAA[G/T]CCTGGTAGGTCTGTT	84182
rs757669147	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30837116	TGCTCCTGTACTGGT[C/T]TCCTAAGCCCTGGCC	84182
rs757671639	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30878199	TTTGGAACAGCCTGG[A/G]CCATGACGTCCGCAG	84182
rs757692965	snp	G/T	1.65864e-05	0.00287974	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782006	TCTAAAAACAAGCCT[G/T]GAACTCATCACCAGA	84182
rs757697612	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30821125	TGTTTCCCATTCCCA[A/T]GCTCCTGTTTATTAT	84182
rs757700979	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30873553	AGTGGGTCTGGGCTG[G/T]GGCCTAAGATTCTCA	84182
rs757704318	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30772276	TGTGTTTTGTCTGTC[C/T]TTGCAGTGTCATACT	84182
rs757707897	snp	A/G	3.33383e-05	0.00408265	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791513	GGTGGTAATTCCAGG[A/G]TGACCCAGGAGAGGC	84182
rs757724821	snp	A/G	3.50306e-05	0.00418498	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875673	TACCCAGATGCTCAC[A/G]TTCACCACAAGTAGG	84182
rs757734675	snp	A/G/T	0.000132688	0.00814409	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791450	GACACCCCAGCAGTG[A/G/T]ACGGCAGCACAGACA	84182
rs757749330	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30854636	CAGAAGGCACTGGAG[A/G]GTTTGGTGGTAAGCC	84182
rs757752384	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30814784	TTATTTAAGTGTAAG[C/T]CTCTTCACCTTTCTA	84182
rs757762829	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30868918	GCTGCAGAGGTTGGT[G/T]TCAGGGCAGCCAGGG	84182
rs757778100	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30832289	CTTAAATACTGTCAC[G/T]TTGTGCCTCCAGGAA	84182
rs757809386	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30858471	AGCGAGGATTTAAAT[C/T]AGGCGGTCAGGCCCC	84182
rs757852306	snp	G/T	1.65679e-05	0.00287814	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778580	AAGGTGTGGTGTGGA[G/T]TCTTGGAACTGAGTT	84182
rs757871168	snp	C/T	1.65671e-05	0.00287807	utr-variant-3-prime, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30892054	CTCATCACCTCATCA[C/T]CGAGGATGACAGCTG	84182
rs757934442	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30800303	AGCAGGGATCTTTTA[C/T]AGGTTAGGATACAGA	84182
rs757981733	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30829818	CAGTGAAAGCTGCTT[A/G]TGTTTGGACACAAGA	84182
rs758007151	snp	A/T	1.65943e-05	0.00288043	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836753	AAACCAATTGACCTC[A/T]CAGTAGCAAAGGTAA	84182
rs758009359	in-del	-/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30860796	ATGTTGTGCACAGCT[-/G]GGGGGACTAGGGCTG	84182
rs758025948	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778814	GCCTGTGGCAGTGCT[C/T]AGCCTCCCGCAGTTA	84182
rs758052989	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30876691	TTCCATGGCTTCAGA[A/G]AGTCCATTGTTCTGT	84182
rs758061210	in-del	-/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30810358	AAAAAAAAAAAAAAG[-/G]TTTATGTGCAAGGTG	84182
rs758062373	snp	A/G	1.71593e-05	0.00292905	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839171	CTTGCTTTTAAAACA[A/G]CCAGTAAAACTCTCT	84182
rs758102962	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30799326	TAAACCAGGGTCCTG[A/T]GACTTTGGAGTCCTT	84182
rs758141877	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30855502	GGAGCCACCAGAGCC[A/G]GGAAAAGGAAGTGAC	84182
rs758184504	snp	A/C	1.92095e-05	0.0030991	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791608	GGTGACGGCTTTTCA[A/C]AAAGAAGCTCCACCT	84182
rs758216127	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30775995	TCTGTTGGCTTTATC[A/T]TCAGAGCACATACAG	84182
rs758236859	snp	A/G	1.65685e-05	0.00287819	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852195	ACTCAGAGGACTCAT[A/G]CACCTTCCTTTCCTT	84182
rs758253844	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30830727	CAAGATGAGATTTGG[A/G]TGGGGACACAGCCAA	84182
rs758255855	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30780835	TACTGAGAGAAAAAG[C/G]AAGAAGGCTACAATA	84182
rs758264483	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30817662	GGAAGCCCGGGTTCC[C/T]GAAGTTTTGTGGTTC	84182
rs758266879	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30806788	AGCTCTGGAGGGTGA[A/G]GCAGATGTGTCTTCC	84182
rs758269493	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30774996	CTTACAACTGCCTAT[G/T]CTACATATCTACTGG	84182
rs758310954	in-del	-/C	1.66409e-05	0.00288447	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882902	GGTGACATGTGTGTG[-/C]CTCTCTCCTCCTTCC	84182
rs758345103	snp	A/T	1.65605e-05	0.0028775	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875460	CAGTAACTGATTCAG[A/T]CTTGATGAGTCTTTC	84182
rs758364078	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852077	AAAGTGGGGAAAAAT[G/T]AGAAACTCTTGGCTC	84182
rs758383463	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30818303	ACTCATGGCTGATAC[A/C]GTTGTCTATTTTATT	84182
rs758417942	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30846438	CTTTTTCCTGCACTT[C/T]ACCTGTGAGGAATTC	84182
rs758422481	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30772412	TTTGCTACTAGTTTG[C/G]AGTGTGAACCTCAGT	84182
rs758447896	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30883526	GTGGGAGCTTCAACT[C/T]CTCTGACCCAGCCCC	84182
rs758448446	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30827766	TAGCTCTTCCATTCA[C/T]GCCCCTTCATACATC	84182
rs758451248	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785425	ACCGCATGACTGTAC[G/T]GAAAGGTTATAGTTT	84182
rs758460760	in-del	-/CTC			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30811908	TGAGTCTTGCCAAAG[-/CTC]CTGGCCGAATAAAGC	84182
rs758472152	snp	A/G	1.66045e-05	0.00288132	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850570	TGTAAGTGGTTCCGA[A/G]GTCTGTGTTGCCGTG	84182
rs758475589	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30879397	CTCCAGCTTCCGGAA[C/T]TCTGAGATAATAAAT	84182
rs758483462	snp	A/C	1.65669e-05	0.00287805	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859273	TTGAAGTGGGCCCCT[A/C]TGGCTGCATCCTGCT	84182
rs758490572	in-del	-/CAT	1.70927e-05	0.00292336	cds-indel, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782185	ATGCAGGATGGAGAA[-/CAT]CATTGTCAGAAACAA	84182
rs758533323	snp	C/G	1.71666e-05	0.00292968	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839355	GGGACCTTTCTGCTG[C/G]GCCATCATGCATAGG	84182
rs758560741	snp	A/G	1.65943e-05	0.00288043	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785754	TTTTTCACAGACATG[A/G]CAATCTTGATGGAGA	84182
rs758582342	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30815832	GCAGGGAGGTGTGAA[C/G]TGGGAGGGCCACAAA	84182
rs758587236	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30773634	CCCAGCTTCTTGAGT[C/T]TGTGGCTCCACTCCT	84182
rs758617278	snp	C/T	2.29761e-05	0.00338932	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859187	CTGGGGTGTGGCTCC[C/T]ACAGAGGTGTGGGGC	84182
rs758630586	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30802836	CAACCAACCAACCAT[C/T]CCAACCGACCAACCA	84182
rs758635172	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30842431	TGCTCCTGACTGGGT[A/G]GAACTTTGCTAAGTA	84182
rs758657504	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30788334	GTACCTTATCAGTTT[C/T]GCTTGATATGTCTTG	84182
rs758674640	snp	A/C	1.65608e-05	0.00287752	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778495	GACCTCAGCATAAAC[A/C]ACAGAAATGATCTTC	84182
rs758687588	snp	A/C	0.0142029	0.0830645	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882382	GGCCCTCACCCCCCC[A/C]CCCACCCAACCCTGT	84182
rs758720795	in-del	-/CAGAGC	0.00016102	0.0089713	cds-indel, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771475	CGTGGGCCTCGTGGG[-/CAGAGC]CAGAGCCAGAGCCAT	84182
rs758781392	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30880747	TTCACTAAGGAATGA[A/G]CTCTGCAGTCCACTT	84182
rs758803651	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30833200	TTAGTCCATTTTCAC[A/G]CTGCTGATAAAAACA	84182
rs758807372	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30780062	AGGAGAAGTAGGCAA[C/T]GGCAGCCCCGTGAAG	84182
rs758827589	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30809177	CACTTTGTTGTCAGT[A/G]TAAACAAGGGTGTAT	84182
rs758831576	snp	A/T	9.95041e-05	0.00705281	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791436	GGGATCCCTCCGAGG[A/T]CACCCCAGCAGTGGA	84182
rs758832862	in-del	-/AT			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30781633	TTTTTAAATGAAGGG[-/AT]ATATATATTTTATAA	84182
rs758842057	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30834198	CTCCATGAGGGCCCC[A/G]CCCCTGTAGCAAACT	84182
rs758873645	snp	A/G	1.65674e-05	0.00287809	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778568	TATGTGCTTTCTAAG[A/G]TGTGGTGTGGAGTCT	84182
rs758890757	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30803894	CTAAGGATCATGGCA[A/T]TTATTTAGGGAAAAG	84182
rs758902166	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30824263	GAGGCTGAGTGTGCT[A/G]ATTCAGATCTGTCTT	84182
rs758919689	snp	C/G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30860444	ATGATTCATTCCTGG[C/G/T]GTGGACTCACGTGCA	84182
rs758938285	snp	A/G	3.31384e-05	0.00407039	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840793	CTGGCAGCTGTCCAA[A/G]GCTGTGTCCTACAGA	84182
rs758991160	snp	C/T	1.65792e-05	0.00287912	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791368	AACCACTGCCAGCAG[C/T]CCTCCCCATCTGCCC	84182
rs759014254	snp	A/G			upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30770951	AAGCAGGCACCAAGG[A/G]GGCGAGGAACATCTC	84182
rs759023373	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30826955	GGGGACTCTTTGAAG[A/C]ATTTCAGCCAGGCTT	84182
rs759061117	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30891020	AGATTTTCTTCAGAA[G/T]TGAAGAAAATCTTCA	84182
rs759092200	in-del	-/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30796123	TTGGAGCACTGTACT[-/T]TTTTTTTTTTTGTCT	84182
rs759136635	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30889982	GGAACCAAATGGTTC[A/G]GGTGATAAAAGGGTA	84182
rs759165258	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30845793	CACGCTGAAATAAAG[G/T]CATCTTGGCAGTGGT	84182
rs759200005	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30869811	TCTCATCTTCTCCAG[A/G]CCCCTCGTGCTGCAG	84182
rs759206455	in-del	-/CTGT			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30822619	TCTTGGTTGACGTGC[-/CTGT]CTGTCTATTTTATTT	84182
rs759219809	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30842043	TGAAACACATTTCAC[C/T]AGCACGGATGATTTT	84182
rs759236849	snp	A/G			missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791339	CTTAGTGAACTGACC[A/G]TAGAAAGGCAGAAAA	84182
rs759245598	snp	C/G	0.000132897	0.00815051	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882234	GGTGGTTTGCAGTGA[C/G]AGCCACTTCAGCATC	84182
rs759245689	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30879689	CTTCCTAAAAGGCAG[C/T]CTTTCCTGCCCTCAT	84182
rs759254272	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30831899	TGCTTCTTTTCAATT[C/T]GACATTTAAACCAGG	84182
rs759284557	snp	A/T	1.66073e-05	0.00288156	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30781997	GGAAAATCCTCTAAA[A/T]ACAAGCCTTGAACTC	84182
rs759294830	snp	A/C	1.72979e-05	0.00294086	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791562	GGCAGGGCAGCCAGC[A/C]CGCACCTGTCAGGTG	84182
rs759333756	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30878921	CAGAGCCACCAGCAT[C/T]GCTGATTTTGACACC	84182
rs759365443	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30873957	TGGGGGTCCCTCTGC[A/G]GCCATCAGAGGAGGC	84182
rs759392205	snp	C/T	0.000183133	0.0095673	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859112	TAGGAGGTCAGCCTT[C/T]GGGCCACCCAGCAAC	84182
rs759416100	snp	C/T	1.65655e-05	0.00287793	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791301	CGAGCAACAGCTCCC[C/T]CTCCAGGACCTCCCT	84182
rs759423450	snp	C/T	1.71932e-05	0.00293195	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859117	GGTCAGCCTTCGGGC[C/T]ACCCAGCAACCCCAG	84182
rs759424734	snp	C/G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30779603	GAGGTCTTGCTTTAT[C/G/T]GTCTAGCCTCTCAGC	84182
rs759442726	in-del	-/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30822811	TGGCTAATTTTTGAA[-/T]TTTTTTTTTTTTTGC	84182
rs759452114	snp	C/G	0.000104302	0.00722083	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771579	CTCGCCCCCTCCAAA[C/G]CCCAGGAAGTGGCTC	84182
rs759455595	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30885824	TCCATTAGCTATCCC[C/G]TCATCCCCAGGTCTG	84182
rs759534986	snp	C/G	1.65638e-05	0.00287778	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852270	CAAAGCAGATGGAGT[C/G]TTAGAAACAGTACGA	84182
rs759544724	in-del	-/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30805846	TTAAGGAATAGGGCC[-/G]TTTATTCAGGACAAG	84182
rs759610302	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30865828	CTGAGGCTCCTGGCT[C/T]TCAATCGAAGACCCT	84182
rs759611015	snp	C/T	1.65616e-05	0.00287759	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828696	AAAATCAGTTGCTGC[C/T]GTCTGACAAGGTGGA	84182
rs759613973	snp	A/C/T	3.31242e-05	0.00406955	utr-variant-3-prime, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30892020	ACCGTTGGATGTGGG[A/C/T]AAACCCTGTGGTCCA	84182
rs759644819	in-del	-/GGGC			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30845537	AAAAAAAAAAAAAAA[-/GGGC]AAGCTCTTCTGTTTT	84182
rs759649884	snp	A/G	3.33678e-05	0.00408446	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785732	TCTGTTTTAATGGAA[A/G]TATTCCTTTTTCACA	84182
rs759658053	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30829660	GGTTTGTTTACTCTG[A/C]CTAACTGATCCTAGA	84182
rs759664489	snp	G/T	1.65696e-05	0.00287828	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828751	CGGTAGGTGCAGCGG[G/T]TGCCTCTGTGCTGTG	84182
rs759680459	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30866840	CTTTGGCCAGCTGCT[A/G]ATGAGCCTGGGCCCC	84182
rs759689360	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30799995	TTAGTCATTGGCTGT[A/G]GGCTGCCCATCCTGG	84182
rs759692312	snp	A/G	3.31879e-05	0.00407343	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875615	GCTGCACGCAGTGAT[A/G]TTGGCTTCTTATCTC	84182
rs759714668	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839967	GGTCCGGTTCAGTTT[C/T]TTAAGCCCCAGGAAC	84182
rs759714808	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30788981	GAGGGCCTTGGGCAC[C/T]AGTGGAGTTTGTTGC	84182
rs759788962	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30830507	AACTTACAATCGTGG[C/T]AGAAGGGGAAGCAAA	84182
rs759815193	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30844754	CCTCAGCCACCCTGG[A/G]AGAGGGGAAGGGTGC	84182
rs759830726	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872109	GGAGGGCACAGAACA[C/G]AGCGCTCAGGTTCCC	84182
rs759831063	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30816830	AGGAAATGTCAGGCC[A/G]GCAATTCTAGTCAGG	84182
rs759870382	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30776764	GTAGTGCATATTAGC[A/T]GCTGCCACACTATAC	84182
rs759884487	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30806525	TCCTGAATAGATGGG[A/G]ATTTTGTGAGAAGGA	84182
rs759899954	in-del	-/CATT			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30814030	GACCTTTGGGTCATC[-/CATT]TGGTGCAGTCAGTAA	84182
rs759919453	snp	C/G	1.96922e-05	0.00313779	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882380	CGGGCCCTCACCCCC[C/G]CACCCACCCAACCCT	84182
rs759922485	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30807478	TAAAAGAAGAAAAGA[G/T]AAGTTGAAAGTATCC	84182
rs759927028	in-del	-/T	1.66204e-05	0.00288269	frameshift-variant, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839264	ATGGAAACTTCAGAG[-/T]TTTTTCCTTTAGTAA	84182
rs759951335	snp	G/T	1.6601e-05	0.00288101	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859359	AACTCCCTGGGGCTG[G/T]GCTGGTCTGTCTTGT	84182
rs759960949	in-del	-/AAGGAAAAAAAAAAA			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30809373	GTTCAGAAGTATCCT[-/AAGGAAAAAAAAAAA]AAAAAAAAAGGATGA	84182
rs759980169	in-del	-/GCAG	1.65747e-05	0.00287873	frameshift-variant, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875606	GAGGCATTGCTGCAC[-/GCAG]GCAGTGATATTGGCT	84182
rs760013725	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30862502	AGCCTTGGCTCTCTG[A/G]GGGATACCAGGCTCT	84182
rs760026483	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30825924	CAAGGTGTTGAAAGG[A/G]CTGGTTGTTTCTTGA	84182
rs760037699	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30879922	TGACACACCTGCTTT[C/T]TCTTACTTAGTGATA	84182
rs760045053	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30795544	GGTCACACAGGCCAT[C/G]AGGGTCAGGGACCAG	84182
rs760078806	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30803484	TTCAGGGTCAGATGG[A/T]TGGTGCTAATTGAGA	84182
rs760090618	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782895	CCTGATAGGATGTGG[C/T]CCACCCACATCATTG	84182
rs760095103	snp	A/G	4.96931e-05	0.00498439	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778554	TAAGGAGAACAAGGT[A/G]TGTGCTTTCTAAGGT	84182
rs760095688	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872696	CCTGGCCTCTTCTAT[A/G]TTTGCACAAGGTATT	84182
rs760126063	snp	A/G			downstream-variant-500B	FAM188B, INMT-FAM188B	GRCh38.p7	7:30892774	AATAGGAAAAGTGCA[A/G]TAATCACTCATGAAG	84182
rs760131478	snp	A/T	1.65699e-05	0.00287831	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859257	CTCTCCCCCTCCCAG[A/T]TTGAAGTGGGCCCCT	84182
rs760147514	snp	C/G	1.65836e-05	0.0028795	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882928	CTTCCCAGACACCAC[C/G]CAAACCATCTCTGAG	84182
rs760151909	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30865723	GGCAACCCAAGGGAT[A/G]GGCCCACAGGCTGGA	84182
rs760174280	in-del	-/A	1.66241e-05	0.00288302	frameshift-variant, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30781994	AAAGGAAAATCCTCT[-/A]AAAACAAGCCTTGAA	84182
rs760220191	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30854004	CCAGAGGAGAGCTGT[A/T]CATCCACTCCTGGCC	84182
rs760223565	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30843880	CCTGTTGGGGGTCAT[C/G]ATGTGTGGAGGTGTG	84182
rs760278099	snp	C/T	1.71563e-05	0.0029288	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30781967	ATTTTTTTTTCTCTC[C/T]CAATGATAGGCAAAG	84182
rs760294587	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30802662	CTTAAAAGTGGTAAG[A/T]CTTTCATATAATTGA	84182
rs760305852	in-del	-/CTCT	1.70969e-05	0.00292373	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839181	AAACAACCAGTAAAA[-/CTCT]CTCTTCTTTTTATAG	84182
rs760310849	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30833845	AAGTCCAAAATCCAG[C/T]AGGGCAGTCAAATCT	84182
rs760315469	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30773349	ATTGTGAGACCAGGA[G/T]GCCAAGAAACTTGCC	84182
rs760343774	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30870688	ACAGAGACTCAGGCA[C/T]GTATTTTAGGCTTGT	84182
rs760362933	snp	A/G	1.65666e-05	0.00287802	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30891906	GATGGGCTCTCATCT[A/G]GGACCCTGAAGCTTG	84182
rs760388692	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30826070	TGTTCACATCGCCTT[C/T]TCTTCTCCCTTTACC	84182
rs760392675	in-del	-/ACACACA			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785292	CACACACACACACAC[-/ACACACA]CACCCATTGGCACAC	84182
rs760411623	snp	G/T	2.37318e-05	0.00344461	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850456	TTCTTGTCCGCAGGG[G/T]ACTGCAGCCTTCAGA	84182
rs760470620	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30869952	GCTCTCCAGAGAATT[C/T]CCCTATTCCCCTAGA	84182
rs760473627	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30792998	TCCGTAAGTTAATAC[A/G]TTACATATTCGTATA	84182
rs760476241	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30847968	AAACTCCTGGCCTCA[A/T]GCGATCCTCCCACCT	84182
rs760488318	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872653	GCATGGGCCAGGGGA[C/G]CCTGGGTCCAGCTGG	84182
rs760507552	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30860217	GTGGTGCCCAGGGGC[A/G]GGAGGTCACAGCAGG	84182
rs760532444	snp	C/T	2.53566e-05	0.00356057	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853488	CTTACTCCTGTGGGA[C/T]GTGCGTCACTAAGCC	84182
rs760545033	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30849295	AACCCCCTCCTCTGT[A/G]TTCCTTTGAGCCCTA	84182
rs760555717	snp	C/T	1.66732e-05	0.00288727	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882216	CCCGAGGTTCCCCAT[C/T]TGGGTGGTTTGCAGT	84182
rs760570199	snp	A/G	1.66142e-05	0.00288216	stop-gained, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839253	TTTCAATGAAGAATG[A/G]AAACTTCAGAGTTTT	84182
rs760572603	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30823879	TTGTTTGAACTGGTT[A/T]GTAGGAATGCTCTGC	84182
rs760584759	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30800857	CTGGGGATGCCTGGC[A/C]GTTTTTCAGGTTTTG	84182
rs760597721	in-del	-/AAG			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30805249	GAGGACGAGGCAGTC[-/AAG]GAGGACTGTGGGCCT	84182
rs760599707	snp	C/T	1.66521e-05	0.00288544	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30786020	CTCTTTCTGTTGTTA[C/T]GGGACTGGAGGCTGA	84182
rs760604822	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839012	GTAAGACCCTCATTA[C/T]TGAGTTTCTCTTTCA	84182
rs760610412	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30867142	CAAAGGTCACGCAGT[A/G]CAGGTGGCAGAAGGG	84182
rs760611204	snp	A/T	9.72242e-05	0.00697156	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853383	CATCCTGAGTGTTTG[A/T]GTCTTCTCAGCTTAC	84182
rs760649883	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853565	CTGTCGTCCCACCCT[G/T]GGATGGCGAGGAAGC	84182
rs760664202	snp	A/G	1.65666e-05	0.00287802	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836710	CCTGTCGCCAGTCCC[A/G]TCAGTGCTCAAGTTG	84182
rs760713222	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30819413	AGACATAATATGTGG[A/G]CTGCTGTATGGTCAA	84182
rs760742997	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30847130	GCCAGGGAGGGCAAC[A/G]GTTTTACCAGAACCT	84182
rs760789693	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30795101	TTGCTCACAGCCCTC[C/G]GTTGGGGTGTGCTGG	84182
rs760792592	in-del	-/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30837618	TTAAATGGCCCCAAA[-/C]CTGGGAGGAGGTGCT	84182
rs760800703	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30818127	GCATGCTAAGAATTA[C/T]TTTTAAAGAAACATA	84182
rs760833177	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30865192	ACTTGCCCTCTCTCA[C/G]CTGAATCTTCCCCCA	84182
rs760835744	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30807518	TTAAAAAAAAAAGCC[A/G]GTCTGGTCTAAGGGA	84182
rs760836028	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778258	CAGCCTTCACTTAGC[C/T]CATGGGGCTGTTGTA	84182
rs760847341	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30820196	GTGAGCCACCGCGCC[C/T]GGCCAATAATTTTTA	84182
rs760871950	in-del	-/AGAGAGAGAGA			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30808942	GTCAAGGAGAGAGAG[-/AGAGAGAGAGA]GAGAGGCAGAGAGAG	84182
rs760897655	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30862624	CAAAGGCCTTTCTCT[A/G]CAGACATTTGGACAC	84182
rs760948743	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30795841	GTGACGTTGGCTGAA[C/T]CCTGCTCAGGCTGCC	84182
rs760969762	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30845854	ATTACGACTCATTCC[A/G]TCAGGCCGGCAGCCG	84182
rs760986122	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30797140	AAATCAAGGTCCCCA[A/T]CCCTGGAGAGCCAGT	84182
rs760986631	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30834461	GACCCTGGGCCCAGC[A/C]CATGAGACCATTTTT	84182
rs760987110	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30808170	AGAGCAGTGCGTGGC[A/G]GGCCCCCGTGGAGGA	84182
rs760990010	snp	A/G	3.31299e-05	0.00406987	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785800	TGTATCATCTAAAAG[A/G]CCCCCGCACAAAAGT	84182
rs760996645	snp	C/T	5.89275e-05	0.00542773	utr-variant-5-prime, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771493	AGCCAGAGCCAGAGC[C/T]ATGGACAGCCTCTTC	84182
rs761076677	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30832633	TCAGGCCTCAGCCTC[C/G]TGAGTAACTGGGATT	84182
rs761081458	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30796963	TTAATTTATTCAACA[A/G]CTATTTAGCAAGGAC	84182
rs761086130	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30880710	CCAGCCACGTCCTGT[A/G]AGACATCTAATTCCC	84182
rs761088585	snp	C/T	9.51611e-05	0.00689721	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882375	TGGTGCGGGCCCTCA[C/T]CCCCCCACCCACCCA	84182
rs761158555	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852827	TCACTGAGAATTTTT[A/G]TTTTAACAAATTAGT	84182
rs761163821	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30841000	CAGCTAGCTGACAAG[G/T]CCTGCGCAGACCAGT	84182
rs761172304	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836918	GAAGAAAATGTGAAC[A/C]GAGAGTCAGGAAAAC	84182
rs761185220	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30811022	AGCACAGGTACCACC[C/G]CTAGAATTTCCAGTA	84182
rs761185622	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30814566	CTACACAGGACTTTC[A/G]TGAGAATTAAATTTT	84182
rs761205013	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828154	AATGTTTTAAGTAAC[A/G]GGAAGATACAGGAGG	84182
rs761210477	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30793337	TATTTTCTTTTTACT[C/G]GAATAACTTCCTTTA	84182
rs761212892	snp	A/G	1.65679e-05	0.00287814	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791327	TCCCTGGGTCAGCTT[A/G]GTGAACTGACCGTAG	84182
rs761294674	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30807957	TCCTTCTTTAACTCA[C/G]TGTCTGAGGGGTTTT	84182
rs761319754	snp	A/G	1.70621e-05	0.00292074	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882319	GACTTGTACTACTAC[A/G]ATGGCCTGGCCAACC	84182
rs761363054	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30844387	ACTCGCCTCCTCCTG[A/G]TGATGGGCCCTGGGC	84182
rs761384868	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30784560	TATCCTGCCGAAGGG[C/T]TTCAGACGTTCCCTG	84182
rs761484406	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30812988	CCTGGCGTCTGCCTT[C/G]CTTGGGCCATTTCTC	84182
rs761507724	snp	C/T	1.65745e-05	0.00287871	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859249	TCATTTTTCTCTCCC[C/T]CTCCCAGTTTGAAGT	84182
rs761528618	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30876422	GGGGGCTAGGATTCA[A/G]CACATCTTTTTGGAG	84182
rs761548434	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30849431	TCGAAGGAGTCCTGG[G/T]AATATGAAATGGAAA	84182
rs761560904	snp	C/T	1.65811e-05	0.00287929	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859336	AGCTGTGAGTATCTT[C/T]CTCCCTCAACTCCCT	84182
rs761562753	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30860265	CCTGGTTGGGTCTGG[A/T]CGGCGCCCTCCCTGT	84182
rs761666546	snp	C/G	0.000658709	0.0181362	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882132	AGAAAAATGCCCGGA[C/G]CCCTTTCCCTGGGGA	84182
rs761673008	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30800052	TAGATGAGTTTGGCA[A/G]AGGACGATTCTCCAG	84182
rs761678884	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840198	GCCCCGTGATGCCTA[C/G]AGAGATGAGCTCCTC	84182
rs761688599	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30888440	GAGGATGAGAGACCC[A/G]GCTATAAACTGGCTG	84182
rs761711055	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839041	CATCAAATATAAGAA[A/G]AATGAGCCTGAAAAA	84182
rs761723407	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782458	TGTAATCCCAGCACT[A/T]TGGGAGGCCAAGACA	84182
rs761727335	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30812022	TTACTACTGATTTAT[C/T]ATTCTTCTTTTTAAA	84182
rs761745597	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840919	TCCAGAAAAAACAAG[C/G]AAGGAAGCATGTGTG	84182
rs761768100	snp	A/C/G	3.35027e-05	0.00409273	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875643	CTCTCTTTGAGCATT[A/C/G]CAACATGTGCCAGGT	84182
rs761773936	snp	A/G	1.65636e-05	0.00287776	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778540	CTTGAATTTCTCTAT[A/G]AGGAGAACAAGGTAT	84182
rs761795887	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30801149	GTGCCAGCCGGGACT[G/T]GGAGGAGGCTTACAG	84182
rs761806382	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30865861	GCCTGCATCGTCTTC[C/G]CTGGACTGTGGGAGG	84182
rs761854816	snp	C/T	4.97401e-05	0.00498674	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852304	TCTGGAAAATTATCA[C/T]GCAAACTTTGGCTTT	84182
rs761858389	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30807771	TCTGTTCTAATTACC[A/G]GTGCATGCAGCCCGC	84182
rs761858810	snp	C/T	3.15821e-05	0.00397367	utr-variant-5-prime, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771480	GCCTCGTGGGCAGAG[C/T]CAGAGCCAGAGCCAT	84182
rs761903164	in-del	-/C	9.86145e-05	0.00702122	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882374	TGGTGCGGGCCCTCA[-/C]CCCCCCCACCCACCC	84182
rs761975953	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30797264	CCTCTTGGATCTTCC[A/G]CTTCCAGTGAGACGA	84182
rs762011585	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30821946	CACTTAAATTCAGCA[A/G]TTGGTATGATTTTGT	84182
rs762019144	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30865033	AACGGGAGGGGTCCA[C/T]GGGATGCTCGTCAGC	84182
rs762048529	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853220	GGCCAGCCTTTCACT[A/C]ACATACAGGTATGGC	84182
rs762059653	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30827456	GCTCTGACACAAACT[C/T]AGTGTCGACTGCCCC	84182
rs762092373	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875009	ATCGTTTAAGACTCA[C/T]CCAAATGTCACTTCT	84182
rs762119316	snp	C/G	1.65603e-05	0.00287747	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785903	TCGGAGCCTTCCTTG[C/G]ATGTGAAGAGGATGG	84182
rs762122134	snp	C/T	1.65636e-05	0.00287776	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828665	CTGGTACATTGATAT[C/T]TTCTATTTTCCAGGA	84182
rs762147516	in-del	-/CTGGA			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30796259	CTGTCTCTTTTTTAT[-/CTGGA]CCTTGTGTGGAAAAG	84182
rs762153582	snp	C/T	1.67888e-05	0.00289726	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836804	TAAATGTGTCTTGAT[C/T]TGAATGGATATAGAT	84182
rs762170784	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30798158	GGACAGCATGTTGCC[A/G]TATTGAATGCTATAG	84182
rs762172699	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30784837	CAATCACAGCACACA[C/T]GACTGCCCCTCCCAC	84182
rs762200948	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30830190	AGTAAACTCTTGTCA[A/G]CAATTACCTGCCAGC	84182
rs762204024	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30881695	ACTGGAAGGAGGAAA[C/T]TATTTCTGCTCCAAC	84182
rs762217591	snp	C/T	1.66032e-05	0.0028812	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882255	CTTCAGCATCCTCTT[C/T]AGCCTGCAGCCGGGG	84182
rs762305618	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30843323	CAGCATTTGGAGGAG[A/G]AGGGTGGGAGCTGGG	84182
rs762312325	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30888568	CTTTCTGTGCCTGTC[C/T]GCAGTTGTTGGTTGC	84182
rs762312334	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782681	GCATGGTAGCTTGGG[A/T]GATGGAGTGAGACCC	84182
rs762317182	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828378	TGCAGTGAAATTGGC[A/G]AGATAGCCTACATGC	84182
rs762318913	snp	A/T	9.97971e-05	0.00706318	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782133	TCAAGATGCTCAGAG[A/T]CTACACTGGTAAATA	84182
rs762325884	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30803519	GTAGGAGCTTAGAGG[A/G]GAGGGAGGGGGTTTT	84182
rs762352023	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30870080	GATATGAAATGCAGA[C/T]GTTCCTCCCTTTTAA	84182
rs762353593	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30816340	AATGTTCCAGAATCC[A/G]GCCTGACTCAAGGAA	84182
rs762386763	snp	C/T	2.94217e-05	0.00383536	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850543	GGGGCCGAGAGAGAG[C/T]CGTTGTTGCACTGTA	84182
rs762416589	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30835915	CCCTCTCTAGGCCTC[A/G]GTTGTCCCACTATGA	84182
rs762446855	snp	A/G	1.66977e-05	0.00288939	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839297	CAGCCTCATTAAAAT[A/G]CGGCATAGTGCAGAA	84182
rs762476104	snp	A/G	1.67806e-05	0.00289656	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882305	CTGAGAGGCTCTTTG[A/G]CTTGTACTACTACGA	84182
rs762496080	snp	A/T	1.66081e-05	0.00288163	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840751	CAGCAATGGTCTCAT[A/T]CTTTGCAGGGTGGTC	84182
rs762499754	snp	A/G	3.31461e-05	0.00407086	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791238	CCCAAGAAGAGAGCC[A/G]GAAGGTCCCTGAGCT	84182
rs762499975	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30825212	ATGCTTTTAAACTGA[C/T]CTTTTAAACTTTGTA	84182
rs762528967	snp	G/T	5.89918e-05	0.00543069	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859152	GGGCTGGAGGCAGTT[G/T]GCTCAGGGCAGGCTG	84182
rs762589653	snp	A/G	1.65619e-05	0.00287762	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778467	GACCATGGACCAGGA[A/G]CGCCCACGCTCTGAC	84182
rs762612178	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30878821	CCATCCACCCATTTA[C/T]TCAACCAGGAGCACG	84182
rs762650667	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30851655	GAGAACAGATGGGGC[A/T]GGAATTCAATTTCTC	84182
rs762693072	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30820567	TACCGATCTGTGATA[A/T]TTCACATAAGCGGAA	84182
rs762693130	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30842107	CATGCTTGGCATCTT[A/T]AAATTTTTTCCAATG	84182
rs762696536	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30783130	AGACTAAAGGCAAGG[G/T]GTTAGCAGGCCTGGT	84182
rs762705940	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30783427	GTAGCTAGCCCACTT[A/G]CATAGTTAACCAAAA	84182
rs762729165	snp	C/G	0.0020689	0.0320963	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782251	TATTAGTTTCCTATT[C/G]CTGCCATAACAAATT	84182
rs762789523	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30789290	GGACCTGCTTCACTG[C/T]CAAGGGCATTGCTGC	84182
rs762808212	in-del	-/A			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30809059	ATATAAGTAGTTAAG[-/A]AAAAAAAAACAGTGT	84182
rs762813954	snp	C/T	1.6641e-05	0.00288448	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875628	ATATTGGCTTCTTAT[C/T]TCTCTTTGAGCATTA	84182
rs762873745	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30801338	TCTGACTCTTGAGAC[A/G]CACAATACCTATTTC	84182
rs762908365	snp	A/G	1.65652e-05	0.0028779	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791306	AACAGCTCCCCCTCC[A/G]GGACCTCCCTGGGTC	84182
rs763022118	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30829504	CTCTTCATCTCCCTT[G/T]TGAACTCTCCCTTTT	84182
rs763048874	in-del	-/ACCCT			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30815432	TGCTGTGGGCCAGGC[-/ACCCT]ACCCCATCACATCTC	84182
rs763059482	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30837567	TCTCCCCCTTCTTCC[A/G]TTCTCTCTTTTGAAG	84182
rs763084268	snp	C/G	1.65611e-05	0.00287755	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785821	GCACAAAAGTAAGCC[C/G]ATGCAGACGGTCCCG	84182
rs763094312	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30814241	CCTCTTAGAAAGGTC[C/T]CTGAAGCTTAAGCTT	84182
rs763157507	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30809676	AAAGTTTGCTAAAAG[G/T]TAACAGTGTAACATG	84182
rs763232652	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30881804	GTGGGAAGAATTGGT[G/T]AGGAGGTCACTGCCG	84182
rs763238884	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30775457	TGGAACTTCTGTGCC[A/G]TCTTCAGCATGCTGC	84182
rs763241650	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30865642	AGGCTTAGCCTCAGC[G/T]GGAGCTGGAGGTGGA	84182
rs763243892	in-del	-/GGTGAGA			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30851914	CATTTGTCAGTTGTG[-/GGTGAGA]GGTGAGAGTCAGACT	84182
rs763270130	snp	C/T	2.02636e-05	0.00318299	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853366	GTGGGGCTTGGGCCA[C/T]TCATCCTGAGTGTTT	84182
rs763281525	snp	G/T			upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30769748	TTGCTTCCCAAGTGT[G/T]GTACATGTGCCAGTG	84182
rs763319943	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30787814	ATCAGTGGTTCTTAG[A/C]CTTTTAGCCTCAGGC	84182
rs763329360	snp	C/G	1.66222e-05	0.00288285	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859368	GGGCTGGGCTGGTCT[C/G]TCTTGTTCACTGCTG	84182
rs763329987	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30864832	CATGGAGGCCCCCAG[A/G]CTCCTCTCAGTAATG	84182
rs763358072	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30846833	TCTCATAAGGAGCGC[A/G]CAACCTAGATCCCTC	84182
rs763364301	in-del	-/ACACACAC			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785272	CTCTCTCTCTCTGAC[-/ACACACAC]ACACACACACACACA	84182
rs763366444	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30855216	TCTGGAAAATGGAAG[A/T]TGGAGCAGTTATCAG	84182
rs763379072	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30804996	GGTAGACTGCAGGCC[C/T]GACAGGTGCCCCAAG	84182
rs763384362	snp	C/T	1.70804e-05	0.00292232	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840875	CTCTTTCTGGCAATA[C/T]CTTATTTTCCCAAGT	84182
rs763393021	in-del	-/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30824748	CAACTAATTTATTTA[-/T]TTTTTTGTGGAGAGA	84182
rs763415468	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30871981	CTGTTCTCTAGTGTA[G/T]GCAGAGCCCTGGTGC	84182
rs763417171	in-del	-/C	1.77833e-05	0.00298183	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882139	TGCCCGGACCCCTTT[-/C]CCTGGGGACGGCATT	84182
rs763439207	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30816074	GATTAGACTAGATGG[A/T]CTGGATTAGCCTTTT	84182
rs763461332	snp	C/T	3.32751e-05	0.00407878	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791503	CTACTTGCCTGGTGG[C/T]AATTCCAGGATGACC	84182
rs763505776	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30883064	ATGGTTGGGGGTGGT[C/T]AGGCCTGCAGGAAGG	84182
rs763533833	snp	A/G	1.65978e-05	0.00288073	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840756	ATGGTCTCATTCTTT[A/G]CAGGGTGGTCCTTGC	84182
rs763547095	in-del	-/C	1.65978e-05	0.00288073	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840756	TGGTCTCATTCTTTG[-/C]CAGGGTGGTCCTTGC	84182
rs763569941	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30871208	GGTCTCACGTTGCCC[C/T]CCAGAGCCAGCTTCT	84182
rs763592098	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30887196	ATTTTGCCCAGGCTC[C/T]CTGTCCACAGTGCCT	84182
rs763615532	snp	A/C	1.65726e-05	0.00287855	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791240	CAAGAAGAGAGCCGG[A/C]AGGTCCCTGAGCTCT	84182
rs763623765	in-del	-/GAG			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30812270	ATGTGTATGTGTGTT[-/GAG]GGGGGGGGGGTATGT	84182
rs763645690	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30854590	CTTCCCTTTGACCTT[C/G]TGGATGTGGGATCCA	84182
rs763683473	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30869984	GGAGGTCTGGGCATC[C/T]AGGTTTGTAGATTTG	84182
rs763699969	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30868865	GGGTCATCACCCCAG[A/G]CCTTTGGTTCAGGGT	84182
rs763736024	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30779823	TGAGACTTCAGCAGA[G/T]TGGATTCGTATGGTG	84182
rs763756173	snp	A/G	2.78983e-05	0.00373475	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782257	TTTCCTATTGCTGCC[A/G]TAACAAATTACTATG	84182
rs763772665	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30838930	TTTCTCAAGGCCCCT[A/G]TAAGGAGCTTACAAA	84182
rs763774878	snp	C/T	6.68662e-05	0.00578175	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839298	AGCCTCATTAAAATA[C/T]GGCATAGTGCAGAAC	84182
rs763786587	snp	C/T	0.000111037	0.00745025	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859156	TGGAGGCAGTTGGCT[C/T]AGGGCAGGCTGCTCC	84182
rs763812510	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30809047	GAAAGAGAGAGATAT[A/G]TAAGTAGTTAAGAAA	84182
rs763815270	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30848135	GTTTGACAGGGGGTC[G/T]CCTTACTTCCAGATA	84182
rs763871410	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30822162	GTACCCACAAAATTT[A/C]TTTCTTTCTTTCTTT	84182
rs763885730	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30849364	GACCAGCTAGCTTCC[A/G]TATGAGTTTTTTAAA	84182
rs763903105	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30797423	GGTAGCCAGGAAAAC[C/T]TACCAGAGAGGGTTA	84182
rs763950875	snp	C/T	1.65655e-05	0.00287793	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791310	GCTCCCCCTCCAGGA[C/T]CTCCCTGGGTCAGCT	84182
rs763962843	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771756	TTCTGCCGTCGTCAC[C/T]GGGCGCTTCCGCAAG	84182
rs763971103	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30876336	GCCCACCGTACTCCA[C/G]TATGACCTCGTCTTA	84182
rs763972291	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30865832	GGCTCCTGGCTCTCA[A/G]TCGAAGACCCTGTGC	84182
rs764015123	in-del	-/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30846753	AAGACAATTTTTCCA[-/T]TGGACTGGAGGTGGG	84182
rs764017705	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30845884	GGCCTCTCCTCAGTC[A/G]GGAAGGATGGAGCTG	84182
rs764050314	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872185	GCCTGGTCACCTAGC[A/G]AGGTTTGCAACCTGG	84182
rs764051421	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30864954	GGTTCGTGGGGTGAG[A/T]TGTGAACAGGGGCTG	84182
rs764063635	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30774316	TCTCTTTAGTGTTCT[C/T]GTGGATGAATTCTCC	84182
rs764078620	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30848637	TTTTCATAGTGAACC[A/G]TGACCTGGGCCAGTG	84182
rs764083525	in-del	-/TTG			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30776520	CATATCATACTATAC[-/TTG]TTGTCTCTCCCCCTA	84182
rs764087591	snp	C/T	6.6246e-05	0.00575488	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778468	ACCATGGACCAGGAA[C/T]GCCCACGCTCTGACC	84182
rs764113385	snp	C/G	4.97277e-05	0.00498612	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882939	CCACCCAAACCATCT[C/G]TGAGGACACAGACAA	84182
rs764136561	in-del	-/T	1.65814e-05	0.00287931	frameshift-variant, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840768	TTTGCAGGGTGGTCC[-/T]TGCGGAGTCCTGGCA	84182
rs764154548	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839025	TATTGAGTTTCTCTT[C/T]CATCAAATATAAGAA	84182
rs764165333	snp	A/C	0.000331395	0.0128681	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828767	TGCCTCTGTGCTGTG[A/C]CCATCAGGGCCCAAG	84182
rs764176748	snp	C/T	1.65671e-05	0.00287807	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852199	AGAGGACTCATGCAC[C/T]TTCCTTTCCTTTTTA	84182
rs764178739	snp	A/C	1.66529e-05	0.00288551	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875630	ATTGGCTTCTTATCT[A/C]TCTTTGAGCATTACA	84182
rs764203674	snp	G/T	6.62394e-05	0.00575459	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785883	AGAAGATAGACAAGC[G/T]TCACTCGGAGCCTTC	84182
rs764237636	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30884410	AGGGCACCTGCAGGT[C/T]GCTTTCCTTTCATGT	84182
rs764242642	snp	C/G	1.66297e-05	0.0028835	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859370	GCTGGGCTGGTCTGT[C/G]TTGTTCACTGCTGCC	84182
rs764271879	snp	A/C	0.00634914	0.0559845	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882386	CTCACCCCCCCACCC[A/C]CCCAACCCTGTCCCC	84182
rs764276635	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836059	CCAGTTACTTAACTC[C/G]TCTAAGCCTCAGTTT	84182
rs764290462	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30795852	TGAATCCTGCTCAGG[C/T]TGCCTTCTTTCTGCT	84182
rs764294266	snp	C/G			upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771242	GTGAGGCCCCGAGTC[C/G]GGAGCCGTGGACGGG	84182
rs764329637	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30883444	ACACCCTCTGCTTGC[A/G]GAGGAGCCGGAGGAG	84182
rs764345050	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30891319	CATGGTCTCACCTAC[A/G]GTAACTTTTCGTTTT	84182
rs764363614	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30863576	CTTCTCTTCTTTGGC[C/T]CTTGCACCAAAGTCA	84182
rs764382825	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836927	GTGAACCGAGAGTCA[A/G]GAAAACTGCAGTCTA	84182
rs764432387	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30814287	AAATCAAATGCTATT[C/T]GGGTTATTATCATTT	84182
rs764443009	snp	G/T	1.66449e-05	0.00288482	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836653	TGGCCATGGTTTTCT[G/T]TCAGAGGATGTGGAG	84182
rs764471085	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836231	TTCTTTCCCAGTCCT[C/G]TCCTCTTCACCTTTG	84182
rs764498359	snp	A/G	1.68162e-05	0.00289962	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872248	TGTTTTCCAGCATCC[A/G]CCAGGACTTTGATGT	84182
rs764502443	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30773397	ACCATGTAATTCCCC[G/T]GCTCAAACCCCTCTA	84182
rs764512814	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30814608	AGCAAGTGCTAGGAA[A/G]AGTAGAAGGTGTTGC	84182
rs764549721	snp	A/G	4.33896e-05	0.00465757	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850480	CTTCAGATGCCCACC[A/G]GACCCGCTGCCTCGT	84182
rs764575197	snp	A/C/G	3.33374e-05	0.00408262	synonymous-codon, missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791512	TGGTGGTAATTCCAG[A/C/G]ATGACCCAGGAGAGG	84182
rs764624458	snp	A/G			downstream-variant-500B	FAM188B, INMT-FAM188B	GRCh38.p7	7:30892777	AGGAAAAGTGCAATA[A/G]TCACTCATGAAGGGG	84182
rs764630593	in-del	-/ACTTGTACT	5.02365e-05	0.00501156	cds-indel, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882305	CTGAGAGGCTCTTTG[-/ACTTGTACT]ACTACGATGGCCTGG	84182
rs764635720	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852898	CTAACTGAGGGTCTC[A/G]CATTGTTGAATGTTT	84182
rs764637595	snp	A/T			missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782123	CAAAGTGCCATCAAG[A/T]TGCTCAGAGACTACA	84182
rs764637812	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30841250	AACCACACATTCCAG[G/T]CCGCCCCACAGATCA	84182
rs764649250	snp	C/T	1.73727e-05	0.00294721	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840885	CAATATCTTATTTTC[C/T]CAAGTCTTCCCCAGA	84182
rs764676465	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30824142	GTGTCCTACAGTTCT[G/T]GAGGTTGGAAAGTCC	84182
rs764681899	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30780010	CTGGCACCTACAGGA[C/G]CACTCAGGTTGCCAG	84182
rs764706799	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30879039	AAAAATATACACACA[A/G]TCATATCATTCCTTT	84182
rs764738856	snp	C/T	4.97558e-05	0.00498753	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791437	GGATCCCTCCGAGGA[C/T]ACCCCAGCAGTGGAC	84182
rs764742865	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30772151	TCTGGCCTCAGGGTG[C/G]AGATGGGGACCTCGG	84182
rs764755524	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30888453	CCGGCTATAAACTGG[C/T]TGGCTGTCAGCCGCC	84182
rs764755647	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836463	AGGAGCATGGACTCT[C/T]TTGATCTGGTTGCTT	84182
rs764762029	snp	A/G	1.68046e-05	0.00289862	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859134	CCCAGCAACCCCAGG[A/G]CTGGGCTGGAGGCAG	84182
rs764769743	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30780610	TTCAGCACAAAGCTC[A/G]CCTGATTCCAGGAAA	84182
rs764775949	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30812057	ATAACTACAAAAGGG[C/T]ACGTGTACCAGATGC	84182
rs764783222	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30887575	GCAGGGCTTTGAAGC[A/G]TGAGCCAGCGAGGAC	84182
rs764902866	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30800057	GAGTTTGGCAAAGGA[C/T]GATTCTCCAGAAAAG	84182
rs764922269	snp	A/C	5.45643e-05	0.00522295	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853496	TGTGGGATGTGCGTC[A/C]CTAAGCCTTCTGATT	84182
rs764924738	snp	A/G	1.65974e-05	0.0028807	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782000	AAATCCTCTAAAAAC[A/G]AGCCTTGAACTCATC	84182
rs764939963	snp	A/G	1.66026e-05	0.00288115	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882247	GAGAGCCACTTCAGC[A/G]TCCTCTTTAGCCTGC	84182
rs764973349	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839089	AACCATGCTAGAAAA[A/T]GGGCTTCCCTGCTAG	84182
rs764987501	snp	C/G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30781054	GAGAGGAGTAGGAAG[C/G/T]GGGAGGACTTGGCAT	84182
rs765029647	snp	A/G/T	3.34965e-05	0.00409235	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30786042	GGAGGCTGAGAACTG[A/G/T]GCTGGGCTTAAGGCA	84182
rs765048292	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30865511	TCTCTCCCTGGTCCC[A/G]TCCCTGGGAGCCACC	84182
rs765049418	snp	C/T	3.31939e-05	0.0040738	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782115	AAAAATAACAAAGTG[C/T]CATCAAGATGCTCAG	84182
rs765050724	snp	A/C	5.22999e-05	0.00511343	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771580	TCGCCCCCTCCAAAG[A/C]CCAGGAAGTGGCTCT	84182
rs765069574	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840281	TGCTGAAGCAGGCCA[C/T]AAGTGGGGCAGAAGA	84182
rs765078206	in-del	-/C	2.20782e-05	0.00332244	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882411	GTCCCCAAGGAGCCT[-/C]CAGGCTGGTCACAGA	84182
rs765087729	snp	C/T	3.96142e-05	0.00445034	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850567	CACTGTAAGTGGTTC[C/T]GAGGTCTGTGTTGCC	84182
rs765105177	in-del	-/AT			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30876203	TGGCATTCCTCGACC[-/AT]ATATAGTGATGCTTC	84182
rs765105824	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30783047	TTTTTAATCCTCACA[A/G]TAGTTAAAGCAATAC	84182
rs765107223	in-del	-/GA			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30808944	AAGGAGAGAGAGAGA[-/GA]GAGAGAGAGAGAGGC	84182
rs765122769	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30884759	CAAGCACCTCCCAGC[C/G]TGGGCCCAGGATTGG	84182
rs765129047	snp	C/T	8.27972e-05	0.00643364	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875536	GAAAGCTGTGTCCAA[C/T]GTTTTCAACGATGTG	84182
rs765137559	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30818217	TTTAAATCTCTTGAT[A/G]TGAATTACATTATTA	84182
rs765195498	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30808330	ACCTATACCGGCACT[A/T]TGGTTTTTGTTTTTG	84182
rs765236960	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30801190	ATTTGCGGTTCATTG[A/T]CTGTTCCCTGCTTCT	84182
rs765250873	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30775742	CATACAGAAGACATT[C/T]TTATCACCTTGGAGA	84182
rs765254884	snp	C/T	0.000132688	0.00814409	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859244	GGAGCTCATTTTTCT[C/T]TCCCCCTCCCAGTTT	84182
rs765273776	in-del	-/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30810359	AAAAAAAAAAAAAAG[-/T]TTATGTGCAAGGTGT	84182
rs765282463	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30788352	TTGATATGTCTTGCA[C/G]TTTGAAGTTTTTACC	84182
rs765286112	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30830594	GTCCCTTATAAAACC[A/G]TCAAATCTCATGAGA	84182
rs765287774	snp	C/G	3.3157e-05	0.00407154	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791233	CCAACCCCAAGAAGA[C/G]AGCCGGAAGGTCCCT	84182
rs765319037	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30886608	GCTTACGCTTTTGCT[A/G]TCCCAGCCCATTGGA	84182
rs765329703	snp	C/T	5.00104e-05	0.00500027	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785735	GTTTTAATGGAAATA[C/T]TCCTTTTTCACAGAC	84182
rs765368985	snp	C/T	1.65688e-05	0.00287821	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852190	TCTCCACTCAGAGGA[C/T]TCATGCACCTTCCTT	84182
rs765374873	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30891338	ACTTTTCGTTTTGCA[A/G]CTGAACTGTTATTCA	84182
rs765382061	snp	G/T	1.6569e-05	0.00287824	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828753	GTAGGTGCAGCGGGT[G/T]CCTCTGTGCTGTGCC	84182
rs765418860	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872890	AAACTGGGAGCTCAG[C/T]TCTACACCTGGCTTC	84182
rs765430549	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30858487	AGGCGGTCAGGCCCC[A/G]GGACACCAGCTCCAA	84182
rs765484936	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30880428	GAATGAGGAAACTCA[G/T]TTATAAAGTCTGTGG	84182
rs765501222	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30860192	GTGGGGAGGCAGGGT[C/G]AGTAGCCTTGTGGTG	84182
rs765553624	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30837549	CTCCCCTTCTCTCTC[A/G]TATCTCCCCCTTCTT	84182
rs765557855	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30834808	CTCAAGTTTAAAGTT[C/G]TGCAAATCTCTAGGG	84182
rs765599473	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30863793	TGAAGGTTTTTTTTC[C/T]ACTTGATTTCAAGCC	84182
rs765624043	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30870299	CCAGTGATGCTTATC[C/G]GCCCCCCCTCAGGAC	84182
rs765640812	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30786076	CTGGGTTTATTTGGG[G/T]TACCCCACAGGGCAG	84182
rs765647919	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30815754	GAGCAACTCCTGCCT[A/C]TTGTACCAGTCACCT	84182
rs765673624	snp	A/G	1.6563e-05	0.00287771	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785808	CTAAAAGGCCCCCGC[A/G]CAAAAGTAAGCCCAT	84182
rs765702337	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30834095	CAGTAGCCCTCTTCT[C/T]ACAGCTCCACTAGGT	84182
rs765723327	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30864644	TCCTGGTGTGATTGC[C/T]GTGGCCAGGCCTGGG	84182
rs765723631	in-del	-/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30845812	TTGGCAGTGGTGGTG[-/T]TTTTTTCTGCAGGAC	84182
rs765731673	snp	G/T	5.02323e-05	0.00501135	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840854	ACTGTGCTCAGTAAG[G/T]CAGTGCTCTTTCTGG	84182
rs765773204	snp	A/G	6.7113e-05	0.00579241	splice-acceptor-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30781976	TCTCTCCCAATGATA[A/G]GCAAAGGAAAATCCT	84182
rs765788742	in-del	-/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30826354	CCAGATAGCCTCACA[-/T]TGTGTGCTGGGTGAG	84182
rs765811437	in-del	-/A	1.65788e-05	0.00287908	frameshift-variant, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782013	ACAAGCCTTGAACTC[-/A]TCACCAGATACTTTC	84182
rs765829198	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30825892	TCTGGAGGGCTGAAT[C/T]TCCACTGAGCTAAAG	84182
rs765829838	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30804954	GGTGTAGCTGGAGCC[C/T]AGGGGATGTGTGAGT	84182
rs765830749	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30849544	AGAGGTCTCTGCCAT[A/G]TTTGATACAGCTGAC	84182
rs765847894	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30803774	CTTGTTCTTCCCCAG[C/T]GTGTTTTTCTACGGC	84182
rs765849932	in-del	-/T	1.66204e-05	0.00288269	frameshift-variant, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839265	ATGGAAACTTCAGAG[-/T]TTTTCCTTTAGTAAC	84182
rs765881055	in-del	-/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30819893	ACAGCATATAGATAA[-/T]TTTTTTTTTTTTTTT	84182
rs765896113	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30877960	GCTAGGGTTACAGGT[A/G]TGAGCCACTGCGCCT	84182
rs765896796	snp	A/C/G	1.65721e-05	0.0028785	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840780	TCCTTGCGGAGTCCT[A/C/G]GCAGCTGTCCAAGGC	84182
rs765916497	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30790062	GCACAGGGCAAATAC[A/G]CATAGGAGTAGTGAG	84182
rs765918554	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30824683	GGCTTCAGCGATCCT[A/C]CCATTTCAGCCTCCT	84182
rs765922858	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30861399	TGGGTGCTGCTGTGA[A/G]TGCTGTCACCATCCC	84182
rs765926342	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30800933	CAACCCCAGCGATTT[A/G]GTCTCGTTGCCCTTG	84182
rs765936328	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30801352	CACACAATACCTATT[G/T]CCTTTCCAGCATGCC	84182
rs765936387	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771662	GGGCGCCCGTTCCCT[A/G]CCTACTGCCTGCTCC	84182
rs765998881	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30843933	TTATGGGGGGGCCTG[C/T]CTGGCTGGACCAGAG	84182
rs766003863	in-del	-/A			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791884	AATAGTTGATGAGCT[-/A]AAAAAAAATTGCAAA	84182
rs766010866	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782811	TGGAAACTCAGACAG[A/G]ATTTTTATGTTACAA	84182
rs766028116	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30813251	GGGATTGTGCTGCTT[C/T]GATTTTTTCTTTTCT	84182
rs766060187	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30800340	AAGGTGAGACTGAAA[C/T]GAAACTGTTTCCAGG	84182
rs766068730	snp	C/G	1.76883e-05	0.00297386	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882150	CTTTCCCTGGGGACG[C/G]CATTTCACATCAGGC	84182
rs766070633	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30870828	GGGTCTCCTCTCTAA[A/G]TGTTATACCTGGCCT	84182
rs766092036	snp	A/G	1.65627e-05	0.00287769	utr-variant-3-prime, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30892017	GTGACCGTTGGATGT[A/G]GGTAAACCCTGTGGT	84182
rs766097061	snp	G/T			upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30770036	TGTAATCCCAGCACT[G/T]TGGGAGGCCGAGGTG	84182
rs766160792	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30856650	GACTGCATGTATGTC[C/T]ATGGCAGAAGTAGGC	84182
rs766165612	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30884378	ATGTGCTGGTGCTTC[C/T]TTCGTCGGGAGGATT	84182
rs766167580	snp	G/T	1.65685e-05	0.00287819	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836725	ATCAGTGCTCAAGTT[G/T]CAGACAGCATCAAAA	84182
rs766168939	in-del	-/ATAT			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30858653	GTTGATGTTTTAAAA[-/ATAT]ATATATATATATATA	84182
rs766199706	snp	C/T	3.36095e-05	0.00409922	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872281	CCACCAGCCACCTGA[C/T]TGGAGCACATGGCTA	84182
rs766204887	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30838006	CTGGTGGAAAATAAT[A/G]AGTCTGTAGGAAAGG	84182
rs766204953	snp	C/G	3.32497e-05	0.00407722	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791499	AGCTCTACTTGCCTG[C/G]TGGTAATTCCAGGAT	84182
rs766206965	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30821956	CAGCAATTGGTATGA[A/T]TTTGTCACATTTGTT	84182
rs766210044	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852151	GACACATGTGGTTTC[A/G]CCCCGGCTGGAGGGC	84182
rs766217511	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30831838	TATACATACGTACAT[G/T]TATCCTACAAAAAGC	84182
rs766299592	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30884649	TCTGTGTCTCTCTAC[A/C]CCTCCCAGGGGGTGG	84182
rs766303302	snp	A/G	3.33161e-05	0.00408129	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30786021	TCTTTCTGTTGTTAT[A/G]GGACTGGAGGCTGAG	84182
rs766307495	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30830791	AGGTATTTAGTCTGG[A/G]CTCTGAAGAATGGGC	84182
rs766318213	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30807793	GCAGCCCGCAGTCAC[G/T]TACCCCCTGCTTGCT	84182
rs766353557	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30845980	TGAAGAGCTCTTGAT[A/C]CCCCTGAAGGCCTGG	84182
rs766362941	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30881898	TGCAGAATGAGCAGT[A/C]CTGGGAACCATTAGA	84182
rs766363091	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30790390	TGTAAGCAGCCTCAC[A/G]GCAGTTAAGAATTTA	84182
rs766383337	snp	A/G	1.6914e-05	0.00290805	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836814	TTGATTTGAATGGAT[A/G]TAGATGGCGTGATTT	84182
rs766384009	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30838903	AAGATCCCTTGCAAA[C/T]CTAAAATTTTGTTTC	84182
rs766386595	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875431	GTCTTTCCCCAGTCT[C/T]CTCTCCACTCTTTCA	84182
rs766467661	snp	C/T	1.65721e-05	0.0028785	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852176	GAGGGCACGCCTTCT[C/T]TCCACTCAGAGGACT	84182
rs766468708	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30777580	TGGGTTTTGTCATGT[A/T]TCCCCAGCAGCTAGA	84182
rs766474380	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30837645	TGCTCTGTCATCTGT[C/T]ACCATGCAATGAGTC	84182
rs766512939	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30774177	TTTCATACCTTCTCT[C/G]TCTTCAAACCCTGAA	84182
rs766532086	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30786199	GCCTCCTTTCCTGCC[A/C]TTAGCTTACCCATTT	84182
rs766549684	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30864864	AGAAAAGAGATCACC[A/G]AGCTTTCTGTTCCAG	84182
rs766625671	snp	G/T	3.17496e-05	0.00398419	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850547	CCGAGAGAGAGCCGT[G/T]GTTGCACTGTAAGTG	84182
rs766647495	snp	A/G	2.93277e-05	0.00382923	missense, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771494	GCCAGAGCCAGAGCC[A/G]TGGACAGCCTCTTCG	84182
rs766683730	snp	C/T	1.67343e-05	0.00289255	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839301	CTCATTAAAATACGG[C/T]ATAGTGCAGAACAAG	84182
rs766685294	in-del	-/GCCG			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30878446	GCCTGGCTGTGTCCT[-/GCCG]GACCTCCATGGGCTA	84182
rs766686743	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30803973	TGACATAGAGAGAGC[C/T]AAAGTCTTTCCCTTG	84182
rs766701558	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30883126	GAGGTGTGGTGATTG[G/T]AAAGACACAGGTTTC	84182
rs766728541	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30781151	CCCCATGTCCAGCCA[C/T]GGCTCGGCAAGACTG	84182
rs766740293	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30881903	AATGAGCAGTACTGG[C/G]AACCATTAGATGTGG	84182
rs766772215	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771575	ACGGCTCGCCCCCTC[C/T]AAAGCCCAGGAAGTG	84182
rs766788270	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30843599	GTTTTTGTTACCCCA[A/C]CCCCAGGCCACATCC	84182
rs766808052	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30806273	GGTTGAAAGGGCCCC[A/G]CTTTAGAATTGAACA	84182
rs766817774	snp	C/T	1.65614e-05	0.00287757	stop-gained, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828686	TTTTCCAGGAAAAAT[C/T]AGTTGCTGCCGTCTG	84182
rs766826281	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30871996	GGCAGAGCCCTGGTG[C/T]GGCTGGAGTGGAGGC	84182
rs766840875	in-del	-/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30856525	TACACAGAGTTGGGG[-/T]TTACAGTGGGTTTCT	84182
rs766855597	snp	A/G	1.672e-05	0.00289132	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782152	CACTGGTAAATATAT[A/G]TGACCTTTCAGATGA	84182
rs766869378	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30855217	CTGGAAAATGGAAGA[G/T]GGAGCAGTTATCAGG	84182
rs766879898	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859254	TTTCTCTCCCCCTCC[C/T]AGTTTGAAGTGGGCC	84182
rs766932151	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30811234	TATAGTAACTTATAC[A/T]ATAAGACAGACACCC	84182
rs766945304	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30842690	AGGGTTCATCTGGAC[A/G]TGAAGTGGCTCAGGG	84182
rs766973219	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30801649	GAAACAGCTCCAGTG[C/T]ATGTTACAGGCCACT	84182
rs766982188	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30841108	GGAACGACATCAAAA[A/C]CAATTTCCCTCCTCA	84182
rs766986008	snp	C/G	1.72579e-05	0.00293746	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882325	TACTACTACGATGGC[C/G]TGGCCAACCAGCAGG	84182
rs766988085	snp	A/G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30794401	AGAGCCAGCTCCACC[A/G/T]CTCTGTCCTAAGGAA	84182
rs767009041	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30814324	GACCAAGTAAGGACA[C/T]TGAAACAATTTCATA	84182
rs767009628	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30868467	TATGCAGATTCGAAG[C/T]CCATGCATTGTGCAG	84182
rs767034163	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30868631	CATTCATCTGACCTT[C/G]TGCAAAATTCTGAGC	84182
rs767036873	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30858191	GGATGGTGTTTCTCC[A/G]GGGAGCAGAAGTGAC	84182
rs767038918	snp	A/G/T	0.000119664	0.00773435	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859167	GGCTCAGGGCAGGCT[A/G/T]CTCCCTGGGGTGTGG	84182
rs767039363	snp	A/C/T	0.00113926	0.0238425	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882379	GCGGGCCCTCACCCC[A/C/T]CCACCCACCCAACCC	84182
rs767042128	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30832894	TTAGCCCTACCCCTT[A/G]TACTCTTATTACCTT	84182
rs767108446	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30878974	GCTCCTGTCCCCATC[A/G]CTTTCCCCCTTTCCA	84182
rs767135745	snp	C/G	1.65781e-05	0.00287902	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840770	TGCAGGGTGGTCCTT[C/G]CGGAGTCCTGGCAGC	84182
rs767151607	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30772035	ATTTTAGTCAACAGT[G/T]GGAATTCCAGTGGTT	84182
rs767169383	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30802531	TATTTCTCTGTCTTT[A/G]CTCAGCCATGTCTCT	84182
rs767179684	in-del	-/C	1.65605e-05	0.0028775	frameshift-variant, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778522	CTTCGAAAGGTTTTG[-/C]ATCTTGAATTTCTCT	84182
rs767198351	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30891065	GATGTCTGTTCCCTG[C/T]CCAAACCTCATACTT	84182
rs767226860	in-del	-/TGTATTT			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30820952	GTGAATTAACTGAAA[-/TGTATTT]TGTATTTTTTTTCTA	84182
rs767240502	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778671	GCCTGTCACACTTGC[C/G]GTCAGAGAGAAACGG	84182
rs767251741	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30820795	TGTAAATAGTGCTGC[C/T]GTGAACATTTACGCA	84182
rs767254391	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30831982	CCTGGCCAACATGTC[A/G]TTCTGGAGTGTTTTG	84182
rs767258530	in-del	-/TG			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30817737	TAGGGGCAATGCGTC[-/TG]TTGCCAGGTGATGCC	84182
rs767264500	snp	C/T	1.65699e-05	0.00287831	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791337	AGCTTAGTGAACTGA[C/T]CGTAGAAAGGCAGAA	84182
rs767309519	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30885897	CTGTTCCACTTCCCC[C/G]ATCAATCCCCCATCA	84182
rs767320166	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30887155	CCACTCCCTGCGGAA[C/T]CTCCCGTTCAGCTTC	84182
rs767342789	snp	A/G	9.94893e-05	0.00705229	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852305	CTGGAAAATTATCAC[A/G]CAAACTTTGGCTTTG	84182
rs767376175	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30822026	TATTAATCGTATTTA[C/T]ATATACACGTATTTT	84182
rs767396581	snp	A/C	1.65636e-05	0.00287776	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778548	TCTCTATAAGGAGAA[A/C]AAGGTATGTGCTTTC	84182
rs767399700	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30845696	CCTGGAGGCCCCCAC[C/T]TCAGATGTTGCCCAC	84182
rs767404888	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30848961	ACGTGCCAGCCACTG[G/T]TCCAGGGACCTTACA	84182
rs767413042	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30789174	CTGAGGACCGGTGAA[C/G]CAGAGAGGAGCGCCA	84182
rs767437245	in-del	-/AT	0.000115949	0.00761321	frameshift-variant, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778446	GGGCTTAAAGAAGAC[-/AT]GTGTGACCATGGACC	84182
rs767530316	snp	A/T	3.9265e-05	0.00443068	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853379	CACTCATCCTGAGTG[A/T]TTGTGTCTTCTCAGC	84182
rs767545970	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30809900	AGAAATGTTTAGGCC[A/G]GGCGCAGTGGCTCAC	84182
rs767568773	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30808616	TAAGGGAAACTATGG[A/C]GTACTGTGACACCAG	84182
rs767624216	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30886324	CTCCTGCTCTCAGAG[A/T]GTTTGCCATCAGCCA	84182
rs767624585	in-del	-/CTG			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30786732	ATAGTTTCATTTATT[-/CTG]CTGCTTTTATTTTTT	84182
rs767647374	in-del	-/CCCCCACCCA	9.39011e-05	0.0068514	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882377	GTGCGGGCCCTCACC[-/CCCCCACCCA]CCCAACCCTGTCCCC	84182
rs767702513	snp	G/T	1.66421e-05	0.00288458	utr-variant-5-prime, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771447	GACCCAGTTGCCTGG[G/T]GCTGCGGCCCGGCGT	84182
rs767719331	snp	C/G	1.73842e-05	0.00294819	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872203	GTTTGCAACCTGGGT[C/G]AGGCAGAGCTGTGCT	84182
rs767742748	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30883400	GGCCTGGCCCAGCCT[C/G]GGGGTGGCAGGAGGT	84182
rs767743511	snp	C/T	3.33111e-05	0.00408099	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782139	TGCTCAGAGACTACA[C/T]TGGTAAATATATATG	84182
rs767770387	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30846211	ACCCCCTATTGCAGC[C/T]TTTGACCCTGAGAGG	84182
rs767772648	snp	C/T	1.6768e-05	0.00289546	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872269	ACTTTGATGTCCCCA[C/T]CAGCCACCTGATTGG	84182
rs767780182	snp	C/T	2.90939e-05	0.00381393	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853504	GTGCGTCACTAAGCC[C/T]TCTGATTTCACTGTG	84182
rs767868198	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30825301	GCATAATTGAAGTCT[C/T]CTCTGGTGATGAGAT	84182
rs767873343	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30830225	ATGCAAGGCTCGGTA[A/G]AAGGCAGACCAAGGT	84182
rs767897988	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30844787	AAGAGGGTACCAGAC[C/T]GGGTCAGGACCTGGA	84182
rs767939745	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872112	GGGCACAGAACAGAG[C/T]GCTCAGGTTCCCACC	84182
rs767966442	in-del	-/A			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30806117	CAGAGTTGTTGAGTT[-/A]ACTTGAAATTTATTC	84182
rs767972509	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30826050	CACTCCAATCTCTGC[G/T]TCCATGTTCACATCG	84182
rs767994361	snp	A/C	1.69261e-05	0.00290908	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882314	TCTTTGACTTGTACT[A/C]CTACGATGGCCTGGC	84182
rs768009257	snp	A/G	1.66782e-05	0.0028877	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791516	GGTAATTCCAGGATG[A/G]CCCAGGAGAGGCTGG	84182
rs768009432	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30775084	ACCAAATGTATGGGG[A/G]TTTTTCCTCCATACA	84182
rs768027119	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30845781	CTCCAGGGAAGTCAC[A/G]CTGAAATAAAGGCAT	84182
rs768050866	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30862511	TCTCTGAGGGATACC[A/G]GGCTCTGCTGAAGGT	84182
rs768071286	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30832551	TCTGTTGCCCAGGCT[A/G]GAGTGCAGTGGTGTA	84182
rs768073675	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30889984	AACCAAATGGTTCAG[A/G]TGATAAAAGGGTACC	84182
rs768084970	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30865160	CGTCTCTGCACCGAC[A/G]CCTGGCTTTGTGGCT	84182
rs768097830	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30843182	TTTGTTGAGAGAACA[C/G]ATGGACAAATGAATG	84182
rs768100088	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30854919	GGCCTGTCCCAAAAG[C/T]ATGGATTAGGATGGC	84182
rs768109870	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30787530	TCCTGAGAGCAGGAC[A/G]CTGTTGTGTTTCTGT	84182
rs768120025	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30858978	ATGGAGCTGGCCATG[A/G]CTGTTGCTGTCTTGT	84182
rs768127602	in-del	-/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30790310	GGGTTTGTGGTAGCA[-/C]CCATAAGCAAAAAAC	84182
rs768129586	snp	A/G	1.65776e-05	0.00287898	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782013	ACAAGCCTTGAACTC[A/G]TCACCAGATACTTTC	84182
rs768144626	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30880342	CTTGCCCCAAGCCTT[A/T]GGTTACCCAAGAATT	84182
rs768186012	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30854020	CATCCACTCCTGGCC[A/G]TGAGCTGGGCGGGAC	84182
rs768186750	snp	G/T	1.65603e-05	0.00287747	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785838	TGCAGACGGTCCCGG[G/T]TGAAACTCCTGTGTT	84182
rs768188239	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30877168	AAGCACCAGGGCTCT[C/T]GAGCACCGGATCCTG	84182
rs768190283	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782974	TTTACAAAATGCCTT[C/T]ACAGCAACAGCTAGA	84182
rs768209840	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30804875	TAGAGGGCAGGTCTG[A/G]CAGTTCAGAGAGTGG	84182
rs768231626	snp	A/G	1.65707e-05	0.00287838	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859319	CCTGTCCAGGTCTAC[A/G]GAGCTGTGAGTATCT	84182
rs768342580	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859246	AGCTCATTTTTCTCT[C/T]CCCCTCCCAGTTTGA	84182
rs768363241	snp	A/C	1.78812e-05	0.00299003	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875693	CCACAAGTAGGGGAG[A/C]CTGACTCTCTGGAGC	84182
rs768363899	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30844237	GACATTCTTCAGACT[C/T]CCCTGAGAGGGAGGA	84182
rs768395522	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30878201	TGGAACAGCCTGGGC[C/T]ATGACGTCCGCAGCG	84182
rs768400592	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30835780	TCTGCTCAGCCTTGC[C/T]GGCACCATTGCCTTG	84182
rs768405287	snp	C/T	9.18063e-05	0.00677456	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882373	ATTGGTGCGGGCCCT[C/T]ACCCCCCCACCCACC	84182
rs768406432	snp	C/G	1.66043e-05	0.00288129	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791479	CACGGACAGGATGCC[C/G]TTGAAGCTCTACTTG	84182
rs768420868	snp	C/T	1.65619e-05	0.00287762	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778535	TGCATCTTGAATTTC[C/T]CTATAAGGAGAACAA	84182
rs768456523	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30825005	ATGAGAGGACCTGTG[C/G]TGGGAGGTGGAGGCC	84182
rs768491710	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30825565	AGGGGAAGGATGTGG[A/G]AAATAGAGGCAAGAC	84182
rs768530618	snp	A/G	3.00838e-05	0.00387827	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850423	CCTTGTGTCCACATG[A/G]GCATAAATGCCTTCC	84182
rs768533866	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30889305	TAAGGTGCTTTTAAC[C/G]CAGCAGATGTAATAG	84182
rs768534755	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850348	TGCAGGCCAGAGAAA[A/G]AACAGGCCATCTGCG	84182
rs768548425	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30794219	CCCCTCCATCAGTGC[C/T]CCCTTCCCCTTGTTT	84182
rs768558385	in-del	-/CCCC	0.000104302	0.00722083	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771579	TCGCCCCCTCCAAAG[-/CCCC]CCCAGGAAGTGGCTC	84182
rs768571159	snp	A/G	1.65822e-05	0.00287938	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840829	CTGTTTGAAGGAGAT[A/G]GCAAAGCCGACTGTG	84182
rs768611699	in-del	-/A	1.65679e-05	0.00287814	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828629	TCTTCTCTGCCGTTT[-/A]CATTTCTCTGTCAGT	84182
rs768617542	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30781778	TTCTTTTAGGGTAGA[A/G]ATTTTGTTTTTGTCT	84182
rs768658451	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30781462	GGTGTAAAGTGAGTC[A/G]GTCCTGACTGCCTCT	84182
rs768674391	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30869904	GGCAGTGCTGAGGCT[C/G]TTGTTCCTCTGCTCA	84182
rs768731076	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30847476	TGAAACCAGGTGCCC[A/T]CGGCAGTTGGTTCTA	84182
rs768746544	in-del	-/A/AA			upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30770284	GCGGGACTCTGTCTC[-/A/AA]AAAAAAAAAAAAAAA	84182
rs768810225	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30879459	TTTGTTATGGCAGCC[C/T]GAGCAGACTAATGCA	84182
rs768827893	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778358	TGAACATCAGGAATC[A/G]TTTGCTTGTGCTTTA	84182
rs768828000	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30885886	CAGCTGCCTGCCTGT[A/T]CCACTTCCCCCATCA	84182
rs768849530	in-del	-/AT			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30858655	TGATGTTTTAAAAAT[-/AT]ATATATATATATATA	84182
rs768906690	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30873762	GATCAGGGAGCAGGG[A/G]CTTTTATCCCTCTTG	84182
rs768907381	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30790124	TGTGCTAGTGCCTTG[C/T]ACAGGTCTCATTTCA	84182
rs768926979	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30821803	ATGTCATCTGATAGC[C/T]CTTAGTAGTTAATGA	84182
rs768940108	snp	C/G	6.00018e-05	0.00547698	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853372	CTTGGGCCACTCATC[C/G]TGAGTGTTTGTGTCT	84182
rs768966669	in-del	-/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30816208	GCCAAATTGGAAGAA[-/T]TAGGGAAATAATATG	84182
rs768983149	in-del	-/AGAG			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30808960	GAGAGAGAGAGAGGC[-/AGAG]AGAGAGAAAGAGACA	84182
rs768986840	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30779457	TTGGGCATAGTGTCA[G/T]AGTCAAAAAGAAAAT	84182
rs768998316	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30794357	GTGGGAAAGTGCAGT[A/G]AGATGGCATCAGAGC	84182
rs769002806	snp	A/G	3.31455e-05	0.00407083	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785978	ATGTCTGGGCCCATC[A/G]CCAGCTCCCCACAGG	84182
rs769004648	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30848317	TGGACGGTGGGGTGA[A/G]ATGGAGCAAAACTGC	84182
rs769029515	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30796576	TACATTCTTAACTTC[A/G]TAGACTGTCAGTGCT	84182
rs769031884	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791074	CATTCCTGGGAGAGA[C/T]ATCACATCATGGGCA	84182
rs769038115	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778338	TTATATGAGAATTAT[C/T]TTGGTGAACATCAGG	84182
rs769049827	snp	A/C	3.18659e-05	0.00399148	utr-variant-5-prime, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771476	GTGGGCCTCGTGGGC[A/C]GAGCCAGAGCCAGAG	84182
rs769080059	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30888689	ACTAGCACAACATGC[C/G]TCATGGCTCAGCCCT	84182
rs769085555	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30799422	TGGAATCACTCCCAG[A/C]CCTGAGTATGAGCAT	84182
rs769086036	snp	C/T	0.000110739	0.00744024	stop-gained, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850533	TGGCGGGCAGGGGGC[C/T]GAGAGAGAGCCGTTG	84182
rs769098626	in-del	-/ACACACA			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785288	CACACACACACACAC[-/ACACACA]CACACACCCATTGGC	84182
rs769134528	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30847862	CTTCTGCCTCAGCCT[C/T]CTGAGTATCTGGGAC	84182
rs769142860	snp	A/G	1.65608e-05	0.00287752	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30891985	TCAGTGAACTGGAAC[A/G]GCTCAGACCCCATCC	84182
rs769146485	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30886464	GTCTGGCAGCTTGCT[G/T]GGCTCTACAGAAAGG	84182
rs769177504	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30798028	GCACCTGTCTCTCTC[C/T]TCGAGACTGCTGAAG	84182
rs769193223	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30776537	GTTGTCTCTCCCCCT[A/G]TAGAGTGCAAGCTCC	84182
rs769210883	in-del	-/AC			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30809007	AAAAGAGAAAAAGAG[-/AC]AGAAAATCAAAGAGA	84182
rs769216986	snp	A/G	1.71725e-05	0.00293018	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791177	TAGGATTCTTTTCAC[A/G]GACACTATCTGAGAC	84182
rs769218536	in-del	-/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30866668	CAGGGCTCTGAGGGA[-/T]TAAGTGGGAAGGGTT	84182
rs769242578	snp	C/T	1.66313e-05	0.00288364	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839226	CCTTCTGTTTGGTTC[C/T]AGCTTTTGCTGTTTC	84182
rs769243513	snp	A/G	1.72193e-05	0.00293417	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872329	GGCGCTGTGGGGCCC[A/G]GGTGGTCCTTCCCCC	84182
rs769253367	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30773223	CCCAGCAGTCGTAAC[C/T]AAGAGAGCTGCCACC	84182
rs769256052	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30864480	TCCAGGAACCCAGAC[A/G]TTGTCTTTGGGAATT	84182
rs769277908	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30884161	GGCACAGCAAGCTTA[C/G]GGTTGATGCCCACCA	84182
rs769325854	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782459	GTAATCCCAGCACTT[C/T]GGGAGGCCAAGACAG	84182
rs769341340	snp	C/T			upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771053	GTAGCGTTGGTGGCC[C/T]CAGAGGGGGCCGTGG	84182
rs769382403	snp	A/G	3.27445e-05	0.00404613	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882366	GCTGACCATTGGTGC[A/G]GGCCCTCACCCCCCC	84182
rs769383278	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30861250	CCTCCCCTTCCCCTC[C/T]CCTAAGACGACAGTG	84182
rs769384912	snp	G/T	3.3418e-05	0.00408753	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882297	CTGGAGGACTGAGAG[G/T]CTCTTTGACTTGTAC	84182
rs769408107	snp	C/T	2.31854e-05	0.00340473	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782238	CCATTATTATGTTTA[C/T]TAGTTTCCTATTGCT	84182
rs769415003	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30825814	GTGTATTAGTTTACC[A/G]TTGCTGCCATAACAA	84182
rs769444102	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30876611	TGCTGAGGGGGCTGG[A/G]CAGAGGAGCACTGGA	84182
rs769541356	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30826623	CAGGATACCTTCATG[A/G]GCCTGGATTTTATTT	84182
rs769546757	in-del	-/GCCCCTCCCC	1.65717e-05	0.00287846	utr-variant-3-prime, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30892056	ATCACCTCATCACCG[-/GCCCCTCCCC]AGGATGACAGCTGAA	84182
rs769554555	snp	A/G	1.65734e-05	0.00287862	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840823	AAACTCCTGTTTGAA[A/G]GAGATAGCAAAGCCG	84182
rs769627508	snp	A/G	1.65647e-05	0.00287786	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828657	AGTCTCCTCTGGTAC[A/G]TTGATATTTTCTATT	84182
rs769635282	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30813938	GGAAGGAAGCATAGC[G/T]CTAGGAACCAGTCTT	84182
rs769657899	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30851528	GCACATACTAAGCAC[C/T]ACGTTTTAGATATCG	84182
rs769663316	snp	A/G	1.6686e-05	0.00288838	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859222	AAGAGGGAGGTGCAA[A/G]TGGGATGGAGCTCAT	84182
rs769666479	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30862304	TCGTGGCACTGCCCA[G/T]ATCCCATGAGACAGC	84182
rs769697847	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30772771	TGTCCTGGCTGCATG[A/T]TGGATATCAATTGAC	84182
rs769751946	snp	C/T	3.31455e-05	0.00407083	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778589	TGTGGAGTCTTGGAA[C/T]TGAGTTTGGCACTGC	84182
rs769753547	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30786167	CTACTGTCAATGACA[C/T]GTGGGGCCTTGAGCA	84182
rs769783684	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30889326	GATGTAATAGATGAA[C/G]TCAGTACCCAGGAGC	84182
rs769787419	snp	C/T	6.62701e-05	0.00575593	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859310	TTCTGCCATCCTGTC[C/T]AGGTCTACAGAGCTG	84182
rs769791344	snp	A/G	1.66454e-05	0.00288486	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840737	CCAGTTCTCACTGGC[A/G]GCAATGGTCTCATTC	84182
rs769795352	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859985	TGTATTTGTCACCTG[A/G]GCATGTCACCAGGAA	84182
rs769797531	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30847708	AAATACTCTATATAT[A/G]TGTGTGTGTTTTTTG	84182
rs769816478	snp	A/G	1.6574e-05	0.00287867	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785769	ACAATCTTGATGGAG[A/G]TGTACTTGGTAATTT	84182
rs769822348	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30841855	TAAAACCATAGCTTA[A/T]TCTTGCCAGTTCCTG	84182
rs769856228	in-del	-/C			upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30770541	CAGGGAGAGAGGCCT[-/C]AGGAGAAACCATCCA	84182
rs769882618	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30835988	TCCAGGACAGTGGGA[C/T]GGTAGAGTTACTAGG	84182
rs769893303	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30779804	CTGTAATCCTTTTTT[C/G]AAATGAGACTTCAGC	84182
rs769910820	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30886717	TTCGCCTTCAGAGAA[A/G]AGCATCCTAATTCAA	84182
rs769937333	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30870846	TTATACCTGGCCTCT[A/C]TCTTTGGGGTGTGGT	84182
rs769937474	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30800144	TGTCTGAGGCAGCTG[G/T]GTGGGACACCTGTGG	84182
rs769943507	in-del	-/AATAAT			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30851476	TATGAATAGCTGATA[-/AATAAT]AATAATTGCGAAGTG	84182
rs769956757	snp	A/G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30888172	TGCAGTGATGCCTCT[A/G/T]GGGGGACAGGGCCTT	84182
rs769972417	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30792229	CCAACCTTACATCCT[A/G]AGAATAAATCCCACT	84182
rs770001448	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30798169	TGCCGTATTGAATGC[A/T]ATAGGCCATTGTAAC	84182
rs770017395	snp	A/G	1.65831e-05	0.00287945	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791401	CAAACGGCTGCCCCC[A/G]TGGGACAGGGCCAGG	84182
rs770018783	in-del	-/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30845539	AAAAAAAAAAAAAGG[-/G]CAAGCTCTTCTGTTT	84182
rs770059962	in-del	-/CAGA			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782804	GGAAATCTGGAAACT[-/CAGA]CAGGATTTTTATGTT	84182
rs770060133	snp	A/G	4.96808e-05	0.00498377	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778516	AATGATCTTCGAAAG[A/G]TTTTGCATCTTGAAT	84182
rs770112487	snp	A/G	1.65616e-05	0.00287759	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785960	CTGATTGTGCGAGGC[A/G]TGATGTCTGGGCCCA	84182
rs770185391	snp	A/G	1.77263e-05	0.00297705	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875683	CTCACGTTCACCACA[A/G]GTAGGGGAGCCTGAC	84182
rs770191931	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30799664	CAGCTTGTCTGACCC[A/C]CTGAGTCAGAAGTTT	84182
rs770275107	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30865370	GGCCCCACTAATGAA[A/G]ATTTTCAGCAATGTC	84182
rs770278103	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791794	AATGCTCTAGACAGG[G/T]GTGTCCAACCTTTTG	84182
rs770291568	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875895	GTTTGAAAAGGACTT[C/T]GAGGGATTTCTGCCG	84182
rs770294488	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836562	TTTCACTCAAACCTT[C/T]TACAAACTTAGCAAT	84182
rs770321826	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30775335	TAGAATGGCTCACAG[A/G]ACTCGGAGAAACACT	84182
rs770324936	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30885507	ACAAGAGGGAAACTC[C/T]GTCTCAAAAAAACAA	84182
rs770341491	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30862376	TGTGGGAGTGCGCCC[A/G]TGAATAAGCCATTCT	84182
rs770342051	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30830344	TGCCCAGCAGTGCTT[A/G]AGTGCTTTAATAAGC	84182
rs770346698	in-del	-/CAC	1.75517e-05	0.00296236	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875676	CCAGATGCTCACGTT[-/CAC]CACAAGTAGGGGAGC	84182
rs770351539	snp	A/T	1.65603e-05	0.00287747	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785880	GGGAGAAGATAGACA[A/T]GCTTCACTCGGAGCC	84182
rs770379145	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30855082	GCCAACTGCTGATGC[A/G]GTGCATCCACCGCCT	84182
rs770391410	snp	G/T	1.6636e-05	0.00288405	splice-donor-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836766	TCTCAGTAGCAAAGG[G/T]AAGTGTAAGGAGACT	84182
rs770430538	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30816382	GAAGGAGAAATGTTG[C/G]AACTGATTTCAGATC	84182
rs770433109	snp	G/T	1.66579e-05	0.00288595	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882219	GAGGTTCCCCATCTG[G/T]GTGGTTTGCAGTGAG	84182
rs770469334	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30866462	GGTGTGGGTAGGCTC[A/G]TGTCATTTAGGGGCA	84182
rs770525597	in-del	-/CCT	1.73857e-05	0.00294831	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872343	CAGGTGGTCCTTCCC[-/CCT]CCTCTGTCCCTCAGA	84182
rs770531525	snp	C/G	6.54965e-05	0.00572223	utr-variant-5-prime, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771469	GCCCGGCGTGGGCCT[C/G]GTGGGCAGAGCCAGA	84182
rs770545132	snp	G/T	3.3998e-05	0.00412284	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791548	AAGAGCGTTCAAACG[G/T]CAGGGCAGCCAGCCC	84182
rs770575003	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30804580	ATCTGGCAGAGTTCC[A/C]CAGAGATAGAGTCTG	84182
rs770578561	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30826922	CATGTGATTATTGTT[A/G]TTATTGATGGTGATG	84182
rs770585010	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30773862	CTTTTCACAGTCCCT[C/T]GGGCCTACCATAACC	84182
rs770599639	in-del	-/A	1.68411e-05	0.00290177	frameshift-variant, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839201	TCTTCTTTTTATAGG[-/A]AATAAAGACCCTTCT	84182
rs770599843	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30827923	CTTTTTAACATAGTA[A/G]ATGGGTTTTCAGAGA	84182
rs770614538	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30795505	AGGGTTCTGAGGCCC[A/G]GAGAGGGGCACAGAC	84182
rs770653607	snp	A/G	2.27918e-05	0.0033757	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850463	CCGCAGGGGACTGCA[A/G]CCTTCAGATGCCCAC	84182
rs770655625	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30890750	CGAAGCCTAGGAAAG[A/G]AAGAAAGAGATTCAG	84182
rs770658507	snp	C/T	1.66211e-05	0.00288275	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839265	ATGGAAACTTCAGAG[C/T]TTTTCCTTTAGTAAC	84182
rs770660692	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30829513	TCCCTTTTGAACTCT[C/G]CCTTTTAAACTGAAG	84182
rs770684329	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30846575	GCCAGTGAAGGCGTG[C/T]GCTGAGCTATCTGGT	84182
rs770737439	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30796446	TCTTCCCAGAATACA[A/G]CCTTGAAGTATGATA	84182
rs770761302	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30878839	AACCAGGAGCACGTC[C/G]TCTCCATCAGGAGGA	84182
rs770767515	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30773063	GCACACTAAGGCCCT[A/C]AGAGTAGAAAGGAGT	84182
rs770777365	snp	C/T	1.724e-05	0.00293594	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782190	GGATGGAGAACATCA[C/T]TGTCAGAAACAAGCA	84182
rs770802033	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30802339	CCTGAGAGGGAAGGT[C/T]TCTTAAAATTTTGCA	84182
rs770810009	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30869687	AATGGCCTCATTTTA[A/C]GTTAGTCACCCCTTG	84182
rs770851252	snp	C/G	1.65715e-05	0.00287845	stop-gained, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782089	CAATCCCTGCACTCT[C/G]AGTTCCAAAGAAAAA	84182
rs770854631	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30825038	AGCAGAGGGTCGAGC[C/T]GAGTTCTGCCACTTG	84182
rs770865998	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30891657	GATCATTCATGTCAG[C/T]GGAGGGCCTCAGTGG	84182
rs770876600	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30803192	GACCTCTCATGGCAC[A/T]TGTCACGCTGGAGAG	84182
rs770891210	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30876070	GAAACTTAACTGTCT[C/T]ACAGTTCTGGAGGCT	84182
rs770996554	snp	C/T			upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30769523	GCTGGAACATGAGGG[C/T]CCCTGGACCAAGCAT	84182
rs771014267	in-del	-/AA			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30809377	AGAAGTATCCTAAGG[-/AA]AAAAAAAAAAAAAAA	84182
rs771051640	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30781549	TAGATGCAGAGCTTA[A/C]AAGCTAAAAAAATAT	84182
rs771054268	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30842665	GTTACAGGGGACATG[C/T]ACGGTGCTAAGGGTT	84182
rs771056280	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30832744	TAAACTCGACCTCAG[G/T]TGATCCACCCACCTT	84182
rs771070098	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30822334	CACCACCAAGCCTGG[A/G]TAATTTTTGTATTTT	84182
rs771111353	snp	A/G	1.65669e-05	0.00287805	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778446	GGGCTTAAAGAAGAC[A/G]TGTGTGACCATGGAC	84182
rs771115835	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30830435	GAAACTGAGTAATTT[G/T]TAAAGGAAAGAGGTT	84182
rs771117621	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30891328	ACCTACAGTAACTTT[C/T]CGTTTTGCAACTGAA	84182
rs771118870	snp	C/T	0.00078347	0.0197768	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840723	AACTCTGCCCCAGGC[C/T]AGTTCTCACTGGCAG	84182
rs771122193	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840566	CCCTAGGAGTGGACA[A/G]AGGGTCTTGTCACTC	84182
rs771157275	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30817814	TCCATGTCTGAACAA[C/G]TCTCTCATTCATTAT	84182
rs771170634	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30811648	CACCCTGGCTCTGGT[A/G]GTTAAAGATCGAACC	84182
rs771192830	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30801768	TCTCTGATCTGATGC[G/T]TCTGCAGAGGAAAGA	84182
rs771205981	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839876	ACATGGCTTATACCC[A/G]GTTCCCACATTATAC	84182
rs771206702	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30799916	CCTGGGGAGATGTGG[A/G]GCATGAATTGACTCA	84182
rs771223301	snp	A/G	1.65603e-05	0.00287747	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875530	GACTGGGAAAGCTGT[A/G]TCCAACGTTTTCAAC	84182
rs771227893	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872040	ATGCAGTGAGCTCTA[C/T]TCTAGGAGGCCTGGG	84182
rs771246975	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30776581	CTTTCATCTGTTCAC[G/T]GCTCTGCCTCTAGCA	84182
rs771248885	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30831312	TTACTAGGTTATGTT[A/G]TAATTTTTCAGGGGG	84182
rs771266975	snp	A/G	3.35126e-05	0.00409331	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836628	CGTGAGTCATAACGA[A/G]GGGCTCACATGGCCA	84182
rs771270620	in-del	-/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30841803	CCCAGCAGGTACCCC[-/T]ATTCTCCTGAAGTTA	84182
rs771292697	snp	C/G	3.31279e-05	0.00406975	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785802	TATCATCTAAAAGGC[C/G]CCCGCACAAAAGTAA	84182
rs771354713	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30856018	CTTTGCCCAAAATCA[A/G]TAGCCTCCTTGCTGT	84182
rs771379125	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30779432	CTGTCCAGCAAATGT[A/T]GCTGTGTGGTTGGGC	84182
rs771383451	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30884261	GGGAAATGGGAGGAG[C/T]GCCGAGACATCCTCG	84182
rs771418950	in-del	-/C	4.99671e-05	0.00499811	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836651	CATGGCCATGGTTTT[-/C]TTTCAGAGGATGTGG	84182
rs771427159	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30786869	GAGACAAATGTAAAA[G/T]AAGTTTGTAAAACAA	84182
rs771452858	snp	C/T	4.98649e-05	0.00499299	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882907	CATGTGTGTGCCTCT[C/T]TCCTCCTTCCCAGAC	84182
rs771478570	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30818911	GCTCCTATTGATAAT[A/G]TTTAGTTTTATCCTT	84182
rs771498358	snp	C/T	8.2837e-05	0.00643519	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828748	GCTCGGTAGGTGCAG[C/T]GGGTGCCTCTGTGCT	84182
rs771504394	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30864278	CTTTGTAACTCTCCT[C/T]AAGAGATTAAAAGCA	84182
rs771513032	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30874639	TCACAGGACCACCCA[A/T]TGCCTCATGCCACGT	84182
rs771523513	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30845721	GCCCACCACATCTGG[C/T]GGGGAAATGGTTCTG	84182
rs771592103	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30863371	TGATAGTGTGTGTGC[A/G]GATGGGAGAGATTGG	84182
rs771597050	snp	C/G/T	0.000167571	0.00915209	utr-variant-5-prime, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771459	TGGTGCTGCGGCCCG[C/G/T]CGTGGGCCTCGTGGG	84182
rs771600593	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30835549	CCAGTGGTAGAATCT[A/G]TGTGCTTGTTCAGTG	84182
rs771622124	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30856924	CCACAGACATTGTCT[C/G]AAGAATGTGCACCAT	84182
rs771636350	snp	A/G	5.04821e-05	0.00502379	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850450	TTCCTTTTCTTGTCC[A/G]CAGGGGACTGCAGCC	84182
rs771673173	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30773244	AGCTGCCACCTTGGT[A/G]CCAGGTACCTAGAAG	84182
rs771686692	snp	A/C	1.66056e-05	0.00288141	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840840	AGATAGCAAAGCCGA[A/C]TGTGCTCAGTAAGTC	84182
rs771724536	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30880678	GGAAGCCAAGTTTAC[G/T]TGGGGTTTAGGCACG	84182
rs771728022	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30842721	CGGGCAGCCTGGTGG[A/G]CTGACATTTTCATCT	84182
rs771750781	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30816182	TACCAATTGCGTGCC[C/T]GGGTCTCATATGCCA	84182
rs771761445	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30784585	TCCCTGCAGCTTTCA[C/T]GGTAAACTCCTTAGA	84182
rs771784788	snp	C/T	2.40191e-05	0.0034654	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853481	AGCATGCCTTACTCC[C/T]GTGGGATGTGCGTCA	84182
rs771791805	snp	C/G	1.65855e-05	0.00287967	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859340	GTGAGTATCTTTCTC[C/G]CTCAACTCCCTGGGG	84182
rs771829271	snp	A/C	1.65658e-05	0.00287795	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782065	CTAACAATTTCACTC[A/C]AGATACCCCAATCCC	84182
rs771830979	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30861023	CACACACACAGACAC[A/G]CGAAAACTCACAAAG	84182
rs771832984	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30773895	CCTACCTCTCACCCA[C/T]CCATCCTTATAATTG	84182
rs771854860	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30833827	GGGGCCCAGGCCCTA[C/T]GCAAGTCCAAAATCC	84182
rs771886071	snp	C/T	0.000215264	0.0103723	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785874	CTGCATGGGAGAAGA[C/T]AGACAAGCTTCACTC	84182
rs771892267	snp	G/T	1.70217e-05	0.00291729	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872228	TGTGCTAACAATGCT[G/T]CTTGTGTTTTCCAGC	84182
rs771893304	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30780908	TTTAATCTTAGACAA[A/C]ATAGTTTTTGTTTTT	84182
rs771900669	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30804530	CCCGACAAATATGTA[C/T]TACAGGATTAAGAAA	84182
rs771911478	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30834724	GGATGCCTTTAACAG[C/T]ACTCAAGTCGCCTCT	84182
rs771922404	snp	C/T	3.32497e-05	0.00407722	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882272	GCCTGCAGCCGGGGC[C/T]CCTGCGTGACTGGAG	84182
rs771971186	in-del	-/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30813349	AAAGTGTTCAATCCC[-/C]AGGTCCTGAATTCTG	84182
rs771981738	snp	A/C	1.66078e-05	0.00288161	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791488	GATGCCCTTGAAGCT[A/C]TACTTGCCTGGTGGT	84182
rs771987995	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30870960	GTGTGCCTCCCAGAG[C/T]CAAGTGTGCCTCTCA	84182
rs771992604	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30802541	TCTTTACTCAGCCAT[G/T]TCTCTGTACCTGGCA	84182
rs771998634	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30881418	CAGTGCCCTGCTGCA[C/T]CCTGAATTTCTCTGT	84182
rs772025594	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30792577	TCTTCTTGTGTAAGT[C/T]TTGGCAAGTTGTATT	84182
rs772034924	in-del	-/GGC	1.65956e-05	0.00288054	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859354	CCCTCAACTCCCTGG[-/GGC]TGGGCTGGTCTGTCT	84182
rs772119191	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30824887	TTATGTGAGAGTGGC[C/T]CTTTCCACCAAGCCA	84182
rs772125683	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30878292	CCTGGGGTTCTGGGG[A/C]CCTCACTGGGTATGT	84182
rs772138568	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30866772	GTTGGGAGGGAAGGA[A/G]CTGGACATGGTGGGT	84182
rs772142095	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30890303	CGTAGGGCAGGACTG[C/T]GTCTTGTGTCTAGAC	84182
rs772142250	snp	C/T			upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771201	ATTTGTCCTAGGCCT[C/T]TCAGATGACCAGGGC	84182
rs772196103	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840087	AGCACCCCAACCTGC[C/T]GTTCAGACAATCCTT	84182
rs772226319	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30888827	GCGGGTTGGTTATGT[C/G]TGTAGAAAGCCTCAA	84182
rs772232523	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30868146	ACAGGGAGGCTTTTA[A/G]ATGAAGGGACAAGCT	84182
rs772266822	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30819176	ACAATAATAGGTGCC[C/T]TTATGCTATACACTG	84182
rs772267856	snp	A/C	0.000108454	0.0073631	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859062	CCCTCGCTCTGCTGT[A/C]ATTGTCATTCAGGTT	84182
rs772268953	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30832448	TTTTCCTCCAGAGAA[C/T]ATTCTCAATGTTGGT	84182
rs772330866	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30777081	GTGGTGTAATCATAG[A/C]TCACTGTGGCCTTGA	84182
rs772332774	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778197	CCAGGACTCCTGTGC[A/G]CGAGTCCTGAACTCA	84182
rs772336852	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30884306	TCCGTCCGTCCATCC[A/G]TTCGTCCATCCACCT	84182
rs772351858	snp	A/G	1.68442e-05	0.00290204	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836806	AATGTGTCTTGATTT[A/G]AATGGATATAGATGG	84182
rs772358086	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30789993	TGTGAACACCAGAGG[C/T]GAATTAAGAATGACC	84182
rs772363011	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30807485	AGAAAAGAGAAGTTG[A/G]AAGTATCCATTTTAG	84182
rs772392111	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30794681	TTTGATATCAAGAGA[C/T]GCTTGGAAAATATGT	84182
rs772394468	in-del	-/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30874692	AGCTAGAACTCATAC[-/T]TGGGCTTCCTACTCC	84182
rs772400911	snp	A/C	1.65641e-05	0.00287781	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852238	AGAACACAGCAGTTC[A/C]GTCCAACAGGGAAAT	84182
rs772422045	snp	C/T	4.23864e-05	0.00460341	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771570	AGGTAACGGCTCGCC[C/T]CCTCCAAAGCCCAGG	84182
rs772439516	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30779136	CTATTATAGGCTTTC[A/T]TGGCACCCTCTAGTT	84182
rs772457836	snp	C/G	1.65633e-05	0.00287774	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828668	GTACATTGATATTTT[C/G]TATTTTCCAGGAAAA	84182
rs772459851	in-del	-/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30841758	GATTAAGAAAAAATA[-/T]TTCTAGTACTCCAGA	84182
rs772466344	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30821284	TATGAGTCCTTGATC[A/G]TTCATTCAGTGAAGG	84182
rs772479451	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30819812	ATCACCTTTTAAATG[A/G]CTAGTATACAAGTGG	84182
rs772491382	in-del	-/AAT			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30802556	GTCTCTGTACCTGGC[-/AAT]AATAAGTGCCAAGCA	84182
rs772493964	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30868973	GAGTTTTCACCCCCT[A/G]GTCAAGCCCATCTCT	84182
rs772509060	snp	G/T	1.65603e-05	0.00287747	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875525	CTCCTGACTGGGAAA[G/T]CTGTGTCCAACGTTT	84182
rs772537587	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30834367	AGCCACAGCCTGAGC[C/T]GTACATTGGCCCCTT	84182
rs772561469	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30796821	ACCAACATATGATGT[C/T]TTGCTCTTCATGTTA	84182
rs772589579	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30796884	AGACTCTGAATTCCT[A/G]GAGTCATACCCTCAA	84182
rs772615564	snp	A/C/G	6.64434e-05	0.0057635	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791490	TGCCCTTGAAGCTCT[A/C/G]CTTGCCTGGTGGTAA	84182
rs772627379	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30849772	CTGACAGCCTTATCT[A/G]AAGATCTGAGTGCAT	84182
rs772629617	snp	C/T	9.94744e-05	0.00705176	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852168	CCCGGCTGGAGGGCA[C/T]GCCTTCTCTCCACTC	84182
rs772659888	in-del	-/A			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30808940	GAGTCAAGGAGAGAG[-/A]GAGAGAGAGAGAGAG	84182
rs772662818	snp	A/G	1.77612e-05	0.00297998	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882143	CGGACCCCTTTCCCT[A/G]GGGACGGCATTTCAC	84182
rs772669219	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30878279	CTTCTCACTGCAGCC[C/T]GGGGTTCTGGGGCCC	84182
rs772671203	snp	G/T	1.65658e-05	0.00287795	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791258	GTCCCTGAGCTCTTT[G/T]TCTGCACCCAACAGG	84182
rs772677031	in-del	-/ACACACA			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785290	CACACACACACACAC[-/ACACACA]CACACCCATTGGCAC	84182
rs772684983	in-del	-/G	1.65726e-05	0.00287855	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778591	TGGAGTCTTGGAACT[-/G]AGTTTGGCACTGCCA	84182
rs772687782	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30837261	TGGCCACAGCAGCCT[C/T]TTCTGCAGGGGTGTC	84182
rs772713185	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30834989	TTTCAAACTTTCCCA[C/T]ATTTTCCTGTCTTCT	84182
rs772777970	in-del	-/CT	0.375	0.216506	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839181	AAACAACCAGTAAAA[-/CT]CTCTCTTCTTTTTAT	84182
rs772784105	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30845298	ACATAGCAAACACCT[A/G]CAGAGCCCCTGCCCC	84182
rs772790163	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30794342	TAATTCTTCTAAAGC[G/T]TGGGAAAGTGCAGTG	84182
rs772812266	snp	A/G	0.000195791	0.00989227	splice-acceptor-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850452	CCTTTTCTTGTCCGC[A/G]GGGGACTGCAGCCTT	84182
rs772820108	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30801314	ACATCAGACTATTAA[A/G]GTTCAAAATCTGACT	84182
rs772852915	snp	G/T	3.40536e-05	0.00412621	utr-variant-5-prime, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771444	ACAGACCCAGTTGCC[G/T]GGTGCTGCGGCCCGG	84182
rs772866410	snp	A/G/T	0.000132486	0.008138	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30891949	CTCTCTCCTCACTCT[A/G/T]CGCTTAGGTGGAAGG	84182
rs772870273	snp	A/G			upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30769921	GTAAAACATGTATGT[A/G]GATTTAAAGAAAATA	84182
rs772978025	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30800621	AGTTAAGGGACGCTA[C/T]TGAGGGGGCAGGAGG	84182
rs773005720	snp	C/T	3.54509e-05	0.00421001	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30781962	TAATGATTTTTTTTT[C/T]TCTCCCAATGATAGG	84182
rs773018402	snp	C/T	2.4238e-05	0.00348115	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853483	CATGCCTTACTCCTG[C/T]GGGATGTGCGTCACT	84182
rs773038770	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872625	GCCCAGGACACAGGG[A/G]GTGATGTCTCAGGCA	84182
rs773064486	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30795297	TCAGTCAGCTTCAGA[A/C]ACCTGGGTGTAACTG	84182
rs773069635	snp	A/G	1.68937e-05	0.0029063	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836808	TGTGTCTTGATTTGA[A/G]TGGATATAGATGGCG	84182
rs773078265	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30868489	ATTGTGCAGCCTGCT[C/T]AGTGGCAGAGCCTCT	84182
rs773101560	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30809525	CAGGACAGGACCATC[A/G]ATGGTTCCTCCCAGG	84182
rs773110971	snp	A/C	6.67145e-05	0.00577519	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882214	ACCCCGAGGTTCCCC[A/C]TCTGGGTGGTTTGCA	84182
rs773136590	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30780609	ATTCAGCACAAAGCT[C/T]GCCTGATTCCAGGAA	84182
rs773146835	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30865163	CTCTGCACCGACACC[G/T]GGCTTTGTGGCTCAC	84182
rs773159106	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30819815	ACCTTTTAAATGGCT[A/G]GTATACAAGTGGTAT	84182
rs773234665	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30886423	CTCTGTTGCCCTGCA[A/G]GAACCCCCAAGCCAC	84182
rs773254579	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30790236	AATTTATAATTTTTT[G/T]TTTAATTTTGGAAAG	84182
rs773259783	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30802163	GCTGCTCTGTTAGCT[A/G]TGTTCCAGCAGTTCC	84182
rs773278036	snp	A/G	1.66136e-05	0.00288211	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839249	GCTGTTTCAATGAAG[A/G]ATGGAAACTTCAGAG	84182
rs773346515	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30847734	TTTTGTTGTTTGTTC[A/G]TTTTTGTTTTTGTTT	84182
rs773365949	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30798323	ATCTCATTGGGATTC[A/G]TGTATGGATTGGATG	84182
rs773414961	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30855117	TGGGCAGAGGAGGCC[C/T]GGAGCAGGGGCCTGG	84182
rs773416730	in-del	-/TCTTTA			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30849816	AGTCTGAAGTGTGAC[-/TCTTTA]TCTTCTATCTCCAGC	84182
rs773434958	snp	A/C	0.000127121	0.00797148	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771572	GTAACGGCTCGCCCC[A/C]TCCAAAGCCCAGGAA	84182
rs773459624	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778615	ACTGCCAAAGCACTC[A/G]TGGGCCCTGCCAGTG	84182
rs773514430	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30864654	ATTGCCGTGGCCAGG[C/T]CTGGGCTGCACCATC	84182
rs773514572	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30876060	TGAAACAACAGAAAC[G/T]TAACTGTCTCACAGT	84182
rs773517652	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30866925	CCACCAACTCTCCCC[A/C]TGCCTCCTGGGCTCC	84182
rs773528857	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30774025	AGAGCTGAATGAGAT[C/T]GGAGAGAAACACACA	84182
rs773528989	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30797124	GATTGGCAAATGCAG[C/T]AAATCAAGGTCCCCA	84182
rs773538250	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30811619	GAAATCCACAAGCAG[A/G]CAGCCCAGCGCCACA	84182
rs773542702	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30774405	ATGTCGCTGTCTCCT[G/T]CACCATGCATTTCCC	84182
rs773559665	snp	A/G	4.98302e-05	0.00499125	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30786001	CCCACAGGTGGGGCT[A/G]TTGCTCTTTCTGTTG	84182
rs773586248	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875234	TGCAGCATAGGACAG[G/T]GTCCTGTGAATGGTT	84182
rs773612481	in-del	-/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30809071	AAGAAAAAAAAACAG[-/T]TGTACCCTATTCCTT	84182
rs773619015	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30794722	CCCATTGTGGGGGTT[G/T]TGGCTGTTTGGGGCC	84182
rs773625908	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30816492	GCTGAGAAACCATCA[C/T]CCCGACAGAACAATG	84182
rs773627795	snp	A/G	3.31538e-05	0.00407134	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828737	GGTGCCCTGCGGCTC[A/G]GTAGGTGCAGCGGGT	84182
rs773642285	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30829368	AGCTAGAGACTGCGG[A/G]TGTTGAGACCAAGGA	84182
rs773716048	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30855885	CCCTGCAGTTTAATT[C/G]ATGTTTTTGCTGGAA	84182
rs773730496	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30834368	GCCACAGCCTGAGCT[G/T]TACATTGGCCCCTTT	84182
rs773743964	snp	C/T	4.98037e-05	0.00498993	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840837	AGGAGATAGCAAAGC[C/T]GACTGTGCTCAGTAA	84182
rs773776241	snp	A/G	0.000394341	0.0140362	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882374	TTGGTGCGGGCCCTC[A/G]CCCCCCCACCCACCC	84182
rs773818584	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30863354	GTACATTCGTGGTGG[A/T]GTGATAGTGTGTGTG	84182
rs773819780	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30773180	GACCACGTGCTCCCC[A/G]CAGGGTTTTGCACAG	84182
rs773849633	snp	C/T	1.65701e-05	0.00287833	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778419	AAACAGCGATTCAGC[C/T]TTCTTCCCTCAGGGC	84182
rs773855481	in-del	-/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30816939	GAACTGGCAACTGCA[-/G]GGTATAAACTTAAGA	84182
rs773877123	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30851769	CCCCAAACCCGGCTC[C/T]GATTCCTGGACGTCT	84182
rs773890219	in-del	-/G	6.35344e-05	0.00563588	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771600	AAGTGGCTCTAATTT[-/G]GGGGGGATCATCGGG	84182
rs773903847	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30826947	GTGATGATGGGGACT[C/T]TTTGAAGAATTTCAG	84182
rs773906364	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30862437	GCCTGCTCCTCTCAC[A/G]TGCCAGGCACACTGC	84182
rs773958594	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30790426	GGATTTTAAAAAACC[C/T]TTCATTTTCAGAGGT	84182
rs773997079	snp	A/G/T	1.65784e-05	0.00287905	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859331	TACAGAGCTGTGAGT[A/G/T]TCTTTCTCCCTCAAC	84182
rs774017759	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30842028	AGCTTGGTACTCCAA[A/T]GAAACACATTTCACC	84182
rs774052293	snp	A/T	8.2826e-05	0.00643476	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785791	TGGTAATTTTGTATC[A/T]TCTAAAAGGCCCCCG	84182
rs774073629	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30803199	CATGGCACATGTCAC[A/G]CTGGAGAGAGTTGAC	84182
rs774121544	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771710	GCGCCGCTTTCCCGG[A/G]ACAGGGGAAACTACA	84182
rs774123245	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882901	GGGTGACATGTGTGT[A/G]CCTCTCTCCTCCTTC	84182
rs774125918	snp	C/T	1.7958e-05	0.00299644	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875698	AGTAGGGGAGCCTGA[C/T]TCTCTGGAGCAATGA	84182
rs774153780	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30890822	TGAGGATGAACCATT[C/G]ACTGAAACCTCTTGG	84182
rs774159645	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30815419	CCTGGGACACCTCAT[A/G]CTGTGGGCCAGGCAC	84182
rs774261085	snp	A/C			upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30769537	GCCCCTGGACCAAGC[A/C]TCATACTGTCTCCTG	84182
rs774263848	snp	C/G/T	3.31676e-05	0.00407221	synonymous-codon, missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791407	GCTGCCCCCATGGGA[C/G/T]AGGGCCAGGCCGAGG	84182
rs774282637	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859084	ATTCAGGTTGTTGCA[A/G]TGTCCCATCCTTTAG	84182
rs774297039	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30779530	AAATGATATCTCATG[G/T]GGAAGTCCAATATGC	84182
rs774314848	snp	C/T	4.96849e-05	0.00498397	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778537	CATCTTGAATTTCTC[C/T]ATAAGGAGAACAAGG	84182
rs774318644	snp	G/T	1.66023e-05	0.00288113	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791480	ACGGACAGGATGCCC[G/T]TGAAGCTCTACTTGC	84182
rs774324558	in-del	-/CCGGCTGAC	3.81956e-05	0.00436994	cds-indel, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882348	CCAGCAGGAGCAGAT[-/CCGGCTGAC]CATTGGTGCGGGCCC	84182
rs774336666	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30876170	TCTCTTCTAGCTCTC[A/G]GTGTTTTCTGGCAAT	84182
rs774361898	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30873999	TCACTGGGGCAGGGG[A/T]ATTGGTGTTAACTGA	84182
rs774374351	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30869695	CATTTTAAGTTAGTC[A/G]CCCCTTGAAAGGCTC	84182
rs774404891	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30829561	TATTTAGAACTCTCT[C/T]GTGTGAGAGGTGTAG	84182
rs774466806	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30833745	TTAGTTACTTCCTAG[A/T]TACAATGGGGGTACA	84182
rs774475960	snp	C/G	1.65608e-05	0.00287752	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30891994	TGGAACGGCTCAGAC[C/G]CCATCCTGTGACCGT	84182
rs774483934	snp	C/T	1.6806e-05	0.00289875	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872249	GTTTTCCAGCATCCG[C/T]CAGGACTTTGATGTC	84182
rs774490751	snp	C/T	1.65773e-05	0.00287895	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785983	TGGGCCCATCGCCAG[C/T]TCCCCACAGGTGGGG	84182
rs774501244	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30787972	AAAATAACAGTAGTA[A/T]ACCTGTTGCATGTAA	84182
rs774502933	in-del	-/AT			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30802474	ATGATTTGATAACTC[-/AT]ATTTATATTCATGAA	84182
rs774510639	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30775568	GATTAAATCATTGAC[C/T]ATTGGTGGTTAGCTC	84182
rs774522399	snp	A/G	1.67351e-05	0.00289263	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836794	ACTCCTGGGTTAAAT[A/G]TGTCTTGATTTGAAT	84182
rs774538147	snp	G/T	2.78129e-05	0.00372903	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850534	GGCGGGCAGGGGGCC[G/T]AGAGAGAGCCGTTGT	84182
rs774569480	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30837712	AGGCTCCTAAAGACT[A/G]TGCAGCAGTAGCGTC	84182
rs774592290	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30830502	CAGGAAACTTACAAT[C/T]GTGGCAGAAGGGGAA	84182
rs774592717	in-del	-/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30792663	GTATAATTATATTAT[-/C]CCTCTTATTATCACT	84182
rs774607169	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30788978	AAAGAGGGCCTTGGG[C/T]ACTAGTGGAGTTTGT	84182
rs774629617	in-del	-/T	0.00112442	0.0236843	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30781952	TATATAAATTAATGA[-/T]TTTTTTTTTCTCTCC	84182
rs774657021	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30855226	GGAAGATGGAGCAGT[C/T]ATCAGGTAGCTTCCA	84182
rs774671786	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30776671	GGAGTGAGCATGTGG[A/G]TGATGCTGAACAAAT	84182
rs774675554	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30819527	TTTAGTCTTTATTCT[G/T]ATTAATGTTATTTTT	84182
rs774679636	snp	A/C	4.56017e-05	0.00477481	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853472	CAGGTATGAAGCATG[A/C]CTTACTCCTGTGGGA	84182
rs774681733	snp	A/G	1.65701e-05	0.00287833	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836689	GTTGATAAGGGAAGA[A/G]GTCATCCTGTCGCCA	84182
rs774697131	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30801010	TTCTTAAGCAGTCCA[C/G]GGGGAGAGAGACAAG	84182
rs774709284	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30806432	ACAATGGTTATTTTA[A/G]TAAATATTAGCTTCC	84182
rs774744610	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30830169	CATTTTACTTTGGTT[C/T]GATTCAGTAAACTCT	84182
rs774754911	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30884276	CGCCGAGACATCCTC[A/G]ACATGCTTTGTCCGT	84182
rs774768720	in-del	-/AC			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30861006	GCCACACACAGAGAC[-/AC]ACACACACACAGACA	84182
rs774772899	snp	C/G/T	8.12686e-05	0.00637408	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771569	AAGGTAACGGCTCGC[C/G/T]CCCTCCAAAGCCCAG	84182
rs774775050	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30807368	ATAGTCTCCCTCTGC[C/G]CCTGCTCAGCTCCCT	84182
rs774784494	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872670	CTGGGTCCAGCTGGG[A/G]AGATGATGGCCCTGG	84182
rs774799750	snp	G/T	3.60887e-05	0.00424771	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882368	TGACCATTGGTGCGG[G/T]CCCTCACCCCCCCAC	84182
rs774815091	snp	C/T	1.73282e-05	0.00294343	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872336	TGGGGCCCAGGTGGT[C/T]CTTCCCCCTCCTCTG	84182
rs774831046	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30845745	GGTTCTGTGAAAGCA[A/G]ATGGAGGATGGGATC	84182
rs774874159	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872091	GGTGGGAGCCTCCTC[C/T]GTGGAGGGCACAGAA	84182
rs774921648	snp	A/G	3.16691e-05	0.00397914	utr-variant-5-prime, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771478	GGGCCTCGTGGGCAG[A/G]GCCAGAGCCAGAGCC	84182
rs774960186	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853904	TGGGTGGGTTGGAGG[G/T]CTTAGCAGTGTGATA	84182
rs774967651	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30795536	CTCTCCAGGGTCACA[C/T]AGGCCATCAGGGTCA	84182
rs774971557	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30804623	GATAATTATGCTGTC[A/G]ATATCTGTTGAGTCC	84182
rs775041719	snp	A/C	5.00379e-05	0.00500165	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839293	AACACAGCCTCATTA[A/C]AATACGGCATAGTGC	84182
rs775048135	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30864363	CAACTGTGAGTGTTG[A/G]TTGGAAAGACAGTGA	84182
rs775113296	in-del	-/TT			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30854642	CACTGGAGGGTTTGG[-/TT]TGGTAAGCCGGAGAG	84182
rs775165344	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30833828	GGGCCCAGGCCCTAC[A/G]CAAGTCCAAAATCCA	84182
rs775177043	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30803333	TAAGAATTGAGATGG[A/C]TTCTTGACTTTGCTT	84182
rs775206452	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859181	TGCTCCCTGGGGTGT[A/G]GCTCCCACAGAGGTG	84182
rs775215497	snp	A/G	6.62943e-05	0.00575698	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840824	AACTCCTGTTTGAAG[A/G]AGATAGCAAAGCCGA	84182
rs775223847	in-del	-/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30814287	AAATCAAATGCTATT[-/C]GGGTTATTATCATTT	84182
rs775225433	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30881559	TTCATCCATGAGGAA[A/T]TTCATTCACCCGACA	84182
rs775233930	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30857147	GTCCTCAGGGCTCTG[C/T]TGTGCCCCCGCATAG	84182
rs775234704	snp	C/T	1.67279e-05	0.002892	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882301	AGGACTGAGAGGCTC[C/T]TTGACTTGTACTACT	84182
rs775267181	snp	C/T	1.65853e-05	0.00287964	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791402	AAACGGCTGCCCCCA[C/T]GGGACAGGGCCAGGC	84182
rs775315668	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30879918	ACTTTGACACACCTG[C/G]TTTTTCTTACTTAGT	84182
rs775324097	snp	G/T	4.91063e-05	0.00495487	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782241	TTATTATGTTTATTA[G/T]TTTCCTATTGCTGCC	84182
rs775346231	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30773940	GGTGCAGCTCTTTTG[C/T]GCTTCTCTCCTTTCA	84182
rs775349540	in-del	-/AAAG	0.00584005	0.0537208	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771576	CGGCTCGCCCCCTCC[-/AAAG]CCCAGGAAGTGGCTC	84182
rs775353630	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30834812	AGTTTAAAGTTCTGC[A/G]AATCTCTAGGGCAGA	84182
rs775370060	snp	C/G	1.65633e-05	0.00287774	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778461	ATGTGTGACCATGGA[C/G]CAGGAACGCCCACGC	84182
rs775381723	in-del	-/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30811825	CCTCTCATGCGGACT[-/C]CCTTAGAGTTGTGAG	84182
rs775393966	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30888310	CTGGGGTTATTTGCC[A/G]ATGTCTGAGGACATT	84182
rs775394916	snp	A/G	3.31395e-05	0.00407046	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828759	GCAGCGGGTGCCTCT[A/G]TGCTGTGCCCATCAG	84182
rs775477585	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30780945	TTACTGAAAAGAATA[C/G]TAAAACTGTCCCGGG	84182
rs775491182	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30867033	TGCAAGACCTGATAT[G/T]GTCTAGTCCCTTATT	84182
rs775491270	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872445	TTCAAGCAGCTTTCA[C/T]GTGCCCACCTCTGCT	84182
rs775497563	snp	G/T	1.6631e-05	0.00288362	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875624	AGTGATATTGGCTTC[G/T]TATCTCTCTTTGAGC	84182
rs775517141	in-del	-/AA			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30820383	GCTTTCTTATTTTTT[-/AA]ATTAACCATTTGAAA	84182
rs775518494	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30868396	GAGATGGTGGTCTTA[A/C]CCTCCTGGCCTTACA	84182
rs775572814	snp	A/G	1.65608e-05	0.00287752	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778523	TTCGAAAGGTTTTGC[A/G]TCTTGAATTTCTCTA	84182
rs775653982	snp	A/G	5.01433e-05	0.00500691	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836637	TAACGAAGGGCTCAC[A/G]TGGCCATGGTTTTCT	84182
rs775654526	snp	A/G	1.68434e-05	0.00290197	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872244	CTTGTGTTTTCCAGC[A/G]TCCGCCAGGACTTTG	84182
rs775680867	snp	A/C/T	6.6309e-05	0.00575767	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882937	CACCACCCAAACCAT[A/C/T]TCTGAGGACACAGAC	84182
rs775695336	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30861979	AAGCCCCGCCCAGGG[A/G]CATGCAGTTCAGAGG	84182
rs775735572	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30819385	AATCAGAAACACAGT[C/T]TGGAATTTTTTGAGA	84182
rs775759030	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30885331	TTGAGACCAGCCTAA[C/T]CAACATGGAGACACC	84182
rs775767562	snp	C/T	0.000117455	0.00766249	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850514	GGCCCTCGCAGACAT[C/T]GTGTGGCGGGCAGGG	84182
rs775772058	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30808177	TGCGTGGCAGGCCCC[C/T]GTGGAGGATCAATGT	84182
rs775790151	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30837419	TAAAACTCCTAGGGA[C/T]ACAGCTGACTTCCTT	84182
rs775808610	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30845832	TTCTGCAGGACTGTC[A/T]GGCTTCATTACGACT	84182
rs775809179	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30885793	GGCACTGGGCCAGGG[G/T]AACCTTCTTCCTGGC	84182
rs775855866	snp	C/G	3.2594e-05	0.00403682	utr-variant-5-prime, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771470	CCCGGCGTGGGCCTC[C/G]TGGGCAGAGCCAGAG	84182
rs775860965	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30891113	TTCCAGCCTCAAACT[C/G]TGCACTGTAGAACTG	84182
rs775862178	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30807509	ATTTTAGATTTAAAA[A/C]AAAAAGCCGGTCTGG	84182
rs775862196	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30821374	TTAGTGATGTTTTAG[C/T]TGGGAATTTCAAAGT	84182
rs775864492	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30795728	TCAGCAGGCTGCATT[C/T]CTTCTGGAGCCTCTA	84182
rs775885800	snp	A/C	1.65853e-05	0.00287964	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882986	CTCGAGCTCTGCATC[A/C]GAACCAAGTGAGTCA	84182
rs775889824	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30845883	CGGCCTCTCCTCAGT[C/T]GGGAAGGATGGAGCT	84182
rs775898641	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30883562	ATTTAAGGGGAGGCT[A/G]AGGCTCAGGCCAGGG	84182
rs775910067	snp	A/G	8.28507e-05	0.00643572	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785975	ATGATGTCTGGGCCC[A/G]TCGCCAGCTCCCCAC	84182
rs775919256	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30863375	AGTGTGTGTGCGGAT[A/G]GGAGAGATTGGTGAC	84182
rs775927299	snp	C/G			upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771175	AAATGGAGCCTCGGA[C/G]CGGAGCGGTAATTTG	84182
rs775962382	snp	A/G/T	6.62398e-05	0.00575466	synonymous-codon, missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785881	GGAGAAGATAGACAA[A/G/T]CTTCACTCGGAGCCT	84182
rs775985216	snp	G/T	3.43808e-05	0.00414599	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872323	TCAGGGGGCGCTGTG[G/T]GGCCCAGGTGGTCCT	84182
rs776018195	snp	A/G	1.65778e-05	0.002879	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782096	TGCACTCTCAGTTCC[A/G]AAGAAAAATAACAAA	84182
rs776048704	in-del	-/ATATAATA			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30793694	AGGGCAGGTATTCTC[-/ATATAATA]CATGGTGGGGAGGGG	84182
rs776055715	snp	C/G	2.26755e-05	0.00336708	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850464	CGCAGGGGACTGCAG[C/G]CTTCAGATGCCCACC	84182
rs776062314	snp	A/C	8.30958e-05	0.00644523	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882229	ATCTGGGTGGTTTGC[A/C]GTGAGAGCCACTTCA	84182
rs776077961	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30871948	CAGGGTCCTCTCTAC[C/T]GTGTCACGCTTCAGT	84182
rs776135787	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791677	CTTCTTAGTCTCCTT[A/G]GTCTCTCAGAACAAG	84182
rs776142810	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30804897	AGAGAGTGGAAGAAT[C/T]CCAAGCCGAGGGGAT	84182
rs776175371	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30775143	ATTGGGTGTCGTACA[A/G]TTCAAATCAGTCCTG	84182
rs776189357	in-del	-/GG			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782370	GTGTGTGTGTGTGTG[-/GG]TGCATGTATCTATAT	84182
rs776192176	snp	A/G	1.66629e-05	0.00288638	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882287	TCCTGCGTGACTGGA[A/G]GACTGAGAGGCTCTT	84182
rs776208978	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30805725	AGTCAACTGTCGTGT[A/G]TTGAGGAATGGGAGG	84182
rs776212262	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30855071	TCACTCAGTAGGCCA[A/G]CTGCTGATGCGGTGC	84182
rs776232171	snp	C/T	1.71608e-05	0.00292918	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791554	GTTCAAACGGCAGGG[C/T]AGCCAGCCCGCACCT	84182
rs776244901	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30881650	GCTGCGGCTGAGGTG[A/G]GTGGGCACCTAGTGA	84182
rs776276635	in-del	-/CTA			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30780569	ATTACTCATTAATAT[-/CTA]CTACATAATAATTTT	84182
rs776336450	in-del	-/CTGC			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30844130	GCCCACCCCTACCGG[-/CTGC]CTGCTGCCCCATCAC	84182
rs776353622	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30829883	TCTACTGGAAGGAAG[A/G]CTGTTAGCAATTCTC	84182
rs776360027	in-del	-/TCTT	3.31203e-05	0.00406928	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875470	TTCAGACTTGATGAG[-/TCTT]TCCCCTTTCTCTCAT	84182
rs776392657	snp	C/G	1.66369e-05	0.00288412	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791502	TCTACTTGCCTGGTG[C/G]TAATTCCAGGATGAC	84182
rs776392723	snp	A/G	2.64421e-05	0.00363598	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850527	ATTGTGTGGCGGGCA[A/G]GGGGCCGAGAGAGAG	84182
rs776397943	in-del	-/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30866460	TAGGTGTGGGTAGGC[-/T]CATGTCATTTAGGGG	84182
rs776405326	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30793008	AATACGTTACATATT[C/T]GTATAACTTAGTTAA	84182
rs776443523	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30827613	TTAAGGCAAATGACT[C/T]GACTGAGTTGAGGAG	84182
rs776450232	snp	A/C	3.32596e-05	0.00407783	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839275	CAGAGTTTTTCCTTT[A/C]GTAACACAGCCTCAT	84182
rs776461036	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30888420	GCCAAAATGCCTTAG[A/G]TACCGAGGATGAGAG	84182
rs776476849	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30804735	GTGGGGAAACTGAGG[A/C]ACAAAATGACCAAGC	84182
rs776492662	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30877300	TTCTTGGGTCGAGGG[C/T]GTTGGTCAGAGAGTA	84182
rs776501754	snp	C/G	1.65891e-05	0.00287998	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791224	CAGCTCCACCCAACC[C/G]CAAGAAGAGAGCCGG	84182
rs776511368	snp	C/G	3.31422e-05	0.00407063	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852183	CGCCTTCTCTCCACT[C/G]AGAGGACTCATGCAC	84182
rs776516156	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839927	AAACCCAGGATCAAG[A/G]ATCAGCAGTTGAGCA	84182
rs776545676	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850398	ACTAAGTAGAGCTGC[A/G]CCATCTCAACCTTGT	84182
rs776585783	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30832645	CTCCTGAGTAACTGG[G/T]ATTACAGGCCCGTGC	84182
rs776613660	snp	C/T			upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30769793	ATTTAGGTGAATGCA[C/T]ACCTTTCTGGTTTTG	84182
rs776627041	snp	A/C	1.8591e-05	0.00304879	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782211	GAAACAAGCAAAGCC[A/C]GGTATCTTTTCCCAT	84182
rs776635911	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30861184	TAGAGCCCTGCTATG[A/G]TGTTCGGGCCAGGCA	84182
rs776655298	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30851402	TGGCTGTGAGACCTA[A/G]ATGAGTCAGTATAAA	84182
rs776673010	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30858880	TCAGTTCCACATATG[C/T]TAGAGGGCAGTAATC	84182
rs776674001	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782643	AGGAGTTCAAGGCTG[C/T]AGTGAGTTATGATCA	84182
rs776707155	snp	A/G	1.65811e-05	0.00287929	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875609	GGCATTGCTGCACGC[A/G]GTGATATTGGCTTCT	84182
rs776755432	in-del	-/AA			upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30770285	GCGGGACTCTGTCTC[-/AA]AAAAAAAAAAAAAAA	84182
rs776793940	snp	C/T	1.66181e-05	0.00288249	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882909	TGTGTGTGCCTCTCT[C/T]CTCCTTCCCAGACAC	84182
rs776827202	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30869760	TAGGACTTCAACATA[C/T]GAATTTTAAGGGGAC	84182
rs776837966	in-del	-/AA			upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30770286	GGGACTCTGTCTCAA[-/AA]AAAAAAAAAAAAAAA	84182
rs776851105	in-del	-/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30834597	GGCTACTTATGCAAA[-/T]TTCTGCAGCCAGCTT	84182
rs776875285	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30847521	CCTTCCTTCCTCAGT[A/G]TTTATTTTTTCCAGT	84182
rs776888252	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30808318	CACCCATGGCATACC[C/T]ATACCGGCACTTTGG	84182
rs776913657	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30867228	AAACAGTTGATATCC[A/G]CTGTATCCAAATCCT	84182
rs776924737	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30798079	CTTACACTGACCTGG[A/G]TGGTGCAGCCTACTA	84182
rs776933145	snp	A/G	1.67489e-05	0.00289381	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836630	TGAGTCATAACGAAG[A/G]GCTCACATGGCCATG	84182
rs776934205	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30873796	AACCAGATGGGAAAA[C/T]TCGAACTTGCCTGAA	84182
rs776948952	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30800017	CCATCCTGGAGTGGG[A/G]CGGGCAGTGTGCAAC	84182
rs776958379	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30854030	TGGCCATGAGCTGGG[C/T]GGGACGTGGCCAGGG	84182
rs776978995	snp	A/C	0.00022477	0.0105988	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771576	CGGCTCGCCCCCTCC[A/C]AAGCCCAGGAAGTGG	84182
rs777015054	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30797221	CCACCAGCCAGTCAG[A/C]TGTGAACAAAGCAGA	84182
rs777024244	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30885444	TTGAACCTGGGAGGC[A/G]AAGATTGCAGTGAGC	84182
rs777060718	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30779476	CAAAAAGAAAATGAT[A/G]TAGTTCAGCATTTAT	84182
rs777085080	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30820892	ATAATGCTATTTTTA[A/G]CTTTTTGAGGAACTC	84182
rs777086572	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30790300	GCCTTTACTAGGGTT[A/T]GTGGTAGCACCCATA	84182
rs777094546	snp	A/G	8.28397e-05	0.00643529	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828749	CTCGGTAGGTGCAGC[A/G]GGTGCCTCTGTGCTG	84182
rs777112613	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30863698	CACTGCCTGCCTGGC[C/T]ACTTCATTGTCAGAG	84182
rs777115057	in-del	-/A			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30851143	TCAGCCTGATCCGTC[-/A]AGAGTGGAAGCATCG	84182
rs777130505	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828305	TTCTGGGCAATGATG[A/C]CAAGAACTCGATTTG	84182
rs777174381	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30814000	GGACAGAGAATCAGT[C/G]TCTGTGCCCAAGGAG	84182
rs777179626	in-del	-/T	8.30696e-05	0.00644421	frameshift-variant, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839238	TTCCAGCTTTTGCTG[-/T]TTCAATGAAGAATGG	84182
rs777191726	snp	C/G	1.65952e-05	0.00288051	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859350	TTCTCCCTCAACTCC[C/G]TGGGGCTGGGCTGGT	84182
rs777199959	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875001	AAAATAACATCGTTT[A/G]AGACTCACCCAAATG	84182
rs777201159	in-del	-/TGTGCT			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859353	CCCTCAACTCCCTGG[-/TGTGCT]GGCTGGGCTGGTCTG	84182
rs777298955	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30777837	ACAGGACCCTCACTT[C/T]GCCAACCCCAGATTT	84182
rs777328008	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836499	CCGCTAAGGGTCTGG[A/G]AACTTCAGAACAGAG	84182
rs777363670	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30807295	TTTTGGCAGGTATCT[A/C]GGAATCAACCCCTGG	84182
rs777425328	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30856903	TTTGCCATTGTCAGA[A/G]CACTTCCACAGACAT	84182
rs777428176	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30884879	CTTAGTGTGTGGACA[C/T]GGGCCTGAACCTCCT	84182
rs777442988	snp	A/T	1.65608e-05	0.00287752	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875474	GACTTGATGAGTCTT[A/T]CCCCTTTCTCTCATC	84182
rs777443435	snp	C/T	1.8447e-05	0.00303696	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791125	TGTTTTCCAGCTCCC[C/T]TCAAAGGGTCCTCAC	84182
rs777449516	in-del	-/AAG			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30807582	TTCTGCCTCCAAAGA[-/AAG]AAGAAGTAAAAACTA	84182
rs777450036	snp	A/G	0.000205754	0.0101407	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782186	TGCAGGATGGAGAAC[A/G]TCATTGTCAGAAACA	84182
rs777480632	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30827816	AATGGAGTGCACCAG[A/G]GCAAGATTACGATTG	84182
rs777501235	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30879539	GCACCTGCCTTCCTC[C/T]CCCACCTCAGCCCGC	84182
rs777508096	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30885170	GCATTTGTGGCTCAT[A/G]CTTGGGGAAAGTTTG	84182
rs777508284	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30863109	AAAAACCTCGGGACC[A/C]GATGATCGCCGAGGG	84182
rs777518283	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30847075	GCTTTGGGGGCATCT[A/G]ACCCAGTGTCTGCAT	84182
rs777542370	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30803098	GCCCCATCTTTAAGT[C/T]GTCTGGAATGTTGCC	84182
rs777543354	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30796335	GGCTTAGGTGAGGGG[A/G]GGATGTCTAGCTTTG	84182
rs777621925	snp	A/G	5.80209e-05	0.00538582	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791611	GACGGCTTTTCAAAA[A/G]GAAGCTCCACCTCTC	84182
rs777630282	in-del	-/CTTGT			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30772310	CTAGGGCGATGGGTA[-/CTTGT]CTTGTATGAAAACAC	84182
rs777642776	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30837161	GAAGGACAGGGAGGT[G/T]TTAACAATTCTTCAG	84182
rs777648064	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30804454	GCCTCTTGCTTGTTC[A/G]AATGGTGTTGGGGAG	84182
rs777655132	snp	A/G	1.65625e-05	0.00287766	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828718	CAAGGTGGATGGTGA[A/G]CTGGGTGCCCTGCGG	84182
rs777665135	snp	G/T	3.31334e-05	0.00407009	stop-gained, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859274	TGAAGTGGGCCCCTA[G/T]GGCTGCATCCTGCTC	84182
rs777670123	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30797788	GAGGAAGGCAAGTGT[A/G]GAGGCAGGGAGACCA	84182
rs777686017	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30863249	AGAGACAGCTGAGTC[C/T]CCAGGACCAACTGCA	84182
rs777686098	snp	A/C	0.000132646	0.00814281	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852308	GAAAATTATCACGCA[A/C]ACTTTGGCTTTGTTT	84182
rs777712457	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875705	GAGCCTGACTCTCTG[C/G]AGCAATGAGGAGGGA	84182
rs777730687	in-del	-/C	0.000165752	0.00910212	frameshift-variant, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882958	GGACACAGACAACGA[-/C]CTTGTCCCACCCCTC	84182
rs777742622	in-del	-/GAG			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30889505	TGGGCACTCACTGCC[-/GAG]GAGAAGTCTGACTTC	84182
rs777795562	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30783074	ATACCAATTTATTCT[C/G]TTACAGTTCTGGAGG	84182
rs777803948	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30888994	AGCTCATACGAGGTA[A/C]TTCAGTCTTTCTGAG	84182
rs777804121	in-del	-/CAG	2.90255e-05	0.00380945	cds-indel, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771499	AGCCAGAGCCATGGA[-/CAG]CCTCTTCGTGGAGGA	84182
rs777809030	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853477	ATGAAGCATGCCTTA[C/T]TCCTGTGGGATGTGC	84182
rs777818046	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30861667	TCATAAGATGTAGCT[A/G]TGCTTAGCACAGCTC	84182
rs777824088	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30812626	GTTACATGGGCATCC[A/G]CAAGCTCTTGCACTC	84182
rs777826824	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30772900	AATGAAATCCAGTGT[C/T]CTCACTGACATCCAA	84182
rs777849637	snp	A/T	4.64306e-05	0.004818	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850578	GTTCCGAGGTCTGTG[A/T]TGCCGTGGCTCATCG	84182
rs777867566	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30793863	GGGAAGAATGGCCAG[G/T]TGGGCCAGACCAGCA	84182
rs777885914	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30860865	ACCTGTGGGGAATTA[A/G]TGTGGGGAATGCTGC	84182
rs777902351	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30843022	CATCGATATGGTTAC[C/T]TGTCCACATCTGCCG	84182
rs777902707	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839145	TATGCACACTGAACA[G/T]CGTATTGTTGCTTGC	84182
rs777903597	in-del	-/TG			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30841370	TTCCTGGAACATCTC[-/TG]TGCAGGCACAAATGA	84182
rs777905221	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30847299	TTACTAACTGGAAGC[C/T]AATGAAAAGAATGAG	84182
rs777909859	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30786114	AGAGGGTCTGTGTGT[C/G]GGGTGGGAAGAACAG	84182
rs777928951	in-del	-/CCCCCACCCCACTAAGGGGATGCGAGAGCTTCTATAT			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30843598	GTTTTTGTTACCCCA[lengthTooLong]CCCCCAGGCCACATC	84182
rs777951374	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30800746	CCAGGGGAAGATTAA[C/T]CTGCCTTGTTCTGCT	84182
rs777968878	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30871633	CTCCATTCTGAGGGT[A/G]GAACCACAGTGGTAC	84182
rs778007380	snp	A/C	1.65647e-05	0.00287786	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791264	GAGCTCTTTGTCTGC[A/C]CCCAACAGGACATTC	84182
rs778026295	snp	A/T	2.12877e-05	0.00326242	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859190	GGGTGTGGCTCCCAC[A/T]GAGGTGTGGGGCTGG	84182
rs778058813	in-del	-/C	4.9694e-05	0.00498443	frameshift-variant, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785800	GTATCATCTAAAAGG[-/C]CCCCCGCACAAAAGT	84182
rs778074820	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853198	CCCTGACGACTCCAG[C/T]GGTACCGGCCAGCCT	84182
rs778109600	snp	C/T	4.9722e-05	0.00498583	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875604	TCAGAGGCATTGCTG[C/T]ACGCAGTGATATTGG	84182
rs778123077	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850838	AGCTCTGGGGTGACC[C/T]CTCAGAGGAAGCCTC	84182
rs778127244	snp	G/T	2.10033e-05	0.00324056	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853343	GCTAATTCAGGATGG[G/T]GCACTGCGTGGGGCT	84182
rs778141225	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30890565	GTGTAAAGTATTCAA[A/G]ATATGCAAGGGGAAA	84182
rs778179301	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30878168	CAGCACAGACACAGC[C/T]GTGGGAAGACTGGCA	84182
rs778184548	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30835751	CAAGCCCTCAGCTAC[C/T]CTCTGGAGTTCACTC	84182
rs778237474	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30789650	TGGCTTTGGGAGGAG[A/G]TTTATAGTGCTTAGT	84182
rs778275116	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30834018	TGGTGTTGAGTGTCT[A/G]TGGCTTTTCCAGGCA	84182
rs778287143	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30837221	TAAAGGGCCCCGTGG[C/T]CACAGGGGACCAGGA	84182
rs778298549	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30799108	GCTTGCAGGTTGCAG[C/T]CTGCTGAGCAGACCT	84182
rs778306940	snp	A/G			upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30770741	GGGGAAAATGTACTG[A/G]GCTTGGTTAGAAACC	84182
rs778312582	snp	A/G	1.65679e-05	0.00287814	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778575	TTTCTAAGGTGTGGT[A/G]TGGAGTCTTGGAACT	84182
rs778344792	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30801721	TGTGGTTATTATAAC[C/T]CCAAGGTACCTTCAG	84182
rs778354988	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30886189	TTGTCCATCTTGCTC[A/G]GTAGGTGGGGCTGCA	84182
rs778404836	in-del	-/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30779058	GAAAAGCAAATGGAA[-/C]TGTGTTTTCTTGGGC	84182
rs778413193	snp	C/T	4.97409e-05	0.00498678	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791375	GCCAGCAGCCCTCCC[C/T]ATCTGCCCAGCAAAC	84182
rs778472100	snp	G/T	8.28013e-05	0.0064338	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778504	ATAAACAACAGAAAT[G/T]ATCTTCGAAAGGTTT	84182
rs778487321	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30864110	TTCTTGGCCTTCATT[A/C]CAGCAGCAAGTTCAG	84182
rs778496513	snp	A/G	3.41134e-05	0.00412983	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872225	AGCTGTGCTAACAAT[A/G]CTTCTTGTGTTTTCC	84182
rs778497421	snp	A/G	1.66938e-05	0.00288905	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875637	TCTTATCTCTCTTTG[A/G]GCATTACAACATGTG	84182
rs778520608	in-del	-/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30798397	TTTGCTGAACAACTG[-/T]TAAGAGGGGGGTTGC	84182
rs778533959	snp	C/T	1.86897e-05	0.00305687	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853400	TCTTCTCAGCTTACG[C/T]TTCACAGTTTGACCT	84182
rs778561183	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30854686	TGGAAATGGGACCAG[A/G]ACTAAAGCTCCTGCT	84182
rs778572792	in-del	-/CC			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859689	GGAGATGGCTGAGGG[-/CC]CTCTAGAGCTCGGGA	84182
rs778579854	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30813071	CACTGGGGAGGGAGA[C/T]GATGGTGGGAGAGTG	84182
rs778610983	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30799141	AGGCCTCTCTGGGCC[C/T]CTGTGCTCCTGTCTG	84182
rs778617874	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30816120	GATGAGCTGTATCTA[G/T]GTGATCTCTGAGTAC	84182
rs778655306	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30870860	TCTCTTTGGGGTGTG[A/G]TTGAAGGAAGGGGGC	84182
rs778679988	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30837982	TGAAAAGGAAAAAAA[G/T]AGCTGATTCTGGTGG	84182
rs778685244	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30865020	GTGTGCTGTTCTGAA[C/T]GGGAGGGGTCCATGG	84182
rs778688648	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778734	GTGGGTTTTCCATCT[C/T]GGTCAGCTGGTGCCG	84182
rs778689188	snp	A/C	3.38129e-05	0.00411161	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791542	GCTGGAAAGAGCGTT[A/C]AAACGGCAGGGCAGC	84182
rs778741938	snp	A/G					GRCh38.p7	7:30880513	TTTGTCTCTCCGTTG[A/G]AAAATTCAGGGTGGC	84182
rs778759332	snp	A/G					GRCh38.p7	7:30843710	CAAGGGGGTGTCTGG[A/G]TAGAAAGAAAACTGC	84182
rs778765674	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30845392	GTTTCATTGACTTAT[A/G]TAGTTTTCACATTGA	84182
rs778769808	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30774835	CTCTGGTGGGCTCAA[G/T]GACTTAGTTTATGGC	84182
rs778771889	snp	A/G	2.85694e-05	0.0037794	missense, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771513	ACAGCCTCTTCGTGG[A/G]GGAGGTGGCCGCCTC	84182
rs778772293	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853652	AGGGATCTGGCTCCT[A/G]CCATTGCATCCTCAA	84182
rs778773285	in-del	-/A	1.67792e-05	0.00289643	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836623	TTCTCCGTGAGTCAT[-/A]ACGAAGGGCTCACAT	84182
rs778794425	in-del	-/AGC			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30784161	AAGGGGCTATGAAGA[-/AGC]AGCTCTTCCTCCGAG	84182
rs778795877	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30805466	AAGCTGAATTCCTTG[A/G]AGGGTGGACATTGCC	84182
rs778796915	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30829028	GGCCATTCAGTAATG[A/G]CCTCTTAGTAAGTTA	84182
rs778815509	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30786936	CAAAGTGCCGTATCA[A/G]TCAAATCAGGGAGCC	84182
rs778824665	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30877539	CTGCCTTGCAACTGC[A/C]AGCTCACTAAGGAAG	84182
rs778839691	snp	A/C/G	6.7232e-05	0.00579761	utr-variant-5-prime, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771458	CTGGTGCTGCGGCCC[A/C/G]GCGTGGGCCTCGTGG	84182
rs778887798	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30816992	GTGATAGTTAGTGCA[C/T]GCGATGACTTCTCGA	84182
rs778887926	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30804296	GTTAGTAAAGCCATG[A/G]GATTTCTTTCATTTC	84182
rs778928016	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882606	TACACCACATGGTAA[A/G]GAGCCCTGAATACTA	84182
rs778932996	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30772393	GACGGAGACAATTCA[A/G]ATATTTGCTACTAGT	84182
rs778975138	snp	A/G			upstream-variant-2KB, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30770229	TGTTCACTTGGCAGT[A/G]AGCCGAGATTGCGCC	84182
rs778987557	snp	A/G	1.70023e-05	0.00291563	splice-donor-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872307	GGCTACTGTACACAG[A/G]TCAGGGGGCGCTGTG	84182
rs779006026	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30889242	AAGATGATGAACAGA[A/T]CAAGAAAATTGAAAA	84182
rs779019924	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30881294	TCAAGATGCTAGCAA[C/T]GTGCTGAGGGCCCTG	84182
rs779023168	in-del	-/TG			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30856546	GTGGGTTTCTGTGTC[-/TG]TTACTTCACTGCAGG	84182
rs779043709	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852044	GAGTTCTCTGGGCCC[A/G]GCCTAGTGGGTGAGT	84182
rs779048414	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30855029	TGTCCTTTGCTGCCT[C/G]TCCCCAGCTCTGGTT	84182
rs779056423	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30861871	CCTGATGGGGCTTCT[A/G]TGGTGACACTCACCC	84182
rs779066306	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30806917	CATGTCCCTGCTTCT[G/T]CCTTGAGCCCAGGGT	84182
rs779085699	snp	A/G	6.10203e-05	0.00552326	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859052	CCCTGCATCACCCTC[A/G]CTCTGCTGTCATTGT	84182
rs779098355	snp	C/T	1.65655e-05	0.00287793	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782062	CGGCTAACAATTTCA[C/T]TCAAGATACCCCAAT	84182
rs779124213	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30862801	AGCCGTGTGGCTAAC[C/G]CAGCCTGTGCCTTAG	84182
rs779134525	snp	C/T	1.66194e-05	0.00288261	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839231	TGTTTGGTTCCAGCT[C/T]TTGCTGTTTCAATGA	84182
rs779138495	in-del	-/A			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30873995	CTGTCACTGGGGCAG[-/A]GGGTATTGGTGTTAA	84182
rs779151850	snp	A/G	3.40153e-05	0.0041239	stop-gained, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782180	TGAAGATGCAGGATG[A/G]AGAACATCATTGTCA	84182
rs779184541	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30832308	TGCCTCCAGGAAACA[A/G]TCTGGCTCAAGGCAT	84182
rs779186239	snp	C/T	1.87802e-05	0.00306427	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791598	GCTATGCAAAGGTGA[C/T]GGCTTTTCAAAAAGA	84182
rs779204993	snp	C/T	6.62394e-05	0.00575459	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875517	TCAATCTGCTCCTGA[C/T]TGGGAAAGCTGTGTC	84182
rs779208343	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30841196	TGCGTCCGGGCCTCC[A/C]TTCCCTCCCCACGCT	84182
rs779252956	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30801877	GGAAGGGAAGATGAG[C/T]GATCTTGTATTGTCC	84182
rs779274600	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30831374	AATGAAGGGGTGGGG[A/C]CTTAGTCATCTCTTA	84182
rs779321001	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30842808	ACACTCTTATTCCCC[C/G]TCAAATTGTTTTCAC	84182
rs779343204	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30813698	TTAGCCCAGGGTGTA[C/G]TTGTCCGAACTGGGG	84182
rs779370119	snp	A/G	1.65734e-05	0.00287862	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778408	TTTAAGATGGTAAAC[A/G]GCGATTCAGCTTTCT	84182
rs779373782	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30802825	ATCTGACCACCCAAC[C/T]AACCAACCATCCCAA	84182
rs779396384	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30856954	TAAGCCAAGGAAATA[A/G]GCCAGGTGGGTCTTC	84182
rs779455941	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30833016	TTTTTACTTGACATA[G/T]ATAGCATTGTGTTAT	84182
rs779483506	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30790901	CACCTGCTGCATGAA[C/T]CTGCTCTCTGTAAGG	84182
rs779487885	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875752	TGGACTCCACTTCTC[A/T]GAGCTGGCTGAAATT	84182
rs779502461	snp	A/T	1.65614e-05	0.00287757	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778484	GCCCACGCTCTGACC[A/T]CAGCATAAACAACAG	84182
rs779563876	snp	A/G	6.62581e-05	0.0057554	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852222	CCTTTTTAGGGCTTC[A/G]AGAACACAGCAGTTC	84182
rs779619024	snp	C/T	1.65641e-05	0.00287781	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828728	GGTGAGCTGGGTGCC[C/T]TGCGGCTCGGTAGGT	84182
rs779638418	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30829104	CTCTGGCTGGGAAGG[C/T]CCGTCCTTTTTAAAA	84182
rs779642518	snp	C/T	8.40951e-05	0.00648386	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836613	TCATGTTCTGTTCTC[C/T]GTGAGTCATAACGAA	84182
rs779656286	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30818393	CCTCATTAATCATCA[G/T]TATCTCAACTAACAC	84182
rs779662176	snp	A/G	1.71284e-05	0.00292642	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872220	GGCAGAGCTGTGCTA[A/G]CAATGCTTCTTGTGT	84182
rs779719237	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30833750	TACTTCCTAGATACA[A/G]TGGGGGTACAGGCAG	84182
rs779719265	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30866164	GAGAAGGGGGGCCAC[A/T]CCCAGGCCACTGAAG	84182
rs779736738	snp	C/T	1.65734e-05	0.00287862	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785770	CAATCTTGATGGAGA[C/T]GTACTTGGTAATTTT	84182
rs779745659	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30788553	AAAGCTCTCAAGCTC[A/G]CGGTGGCAGATAGAA	84182
rs779760592	in-del	-/C	1.65647e-05	0.00287786	frameshift-variant, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791298	CTTCGAGCAACAGCT[-/C]CCCCTCCAGGACCTC	84182
rs779792071	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30775030	GTCTAACAAGCATCT[C/T]AACATGTCTCTGATA	84182
rs779807597	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30861054	ACATGGACACACACA[C/G]AGACACATAGTCCAG	84182
rs779821699	snp	C/T	0.000165758	0.00910227	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882961	CACAGACAACGACCT[C/T]GTCCCACCCCTCGAG	84182
rs779822084	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30844927	ATCTTCAAGGGCTCT[A/G]TAAGTGAGTAGGGCC	84182
rs779828376	snp	A/G	3.27552e-05	0.00404679	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850420	CAACCTTGTGTCCAC[A/G]TGGGCATAAATGCCT	84182
rs779840861	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30855553	AGGTGGAGCCTGAGG[G/T]TGATTGCTCAAATGA	84182
rs779843625	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30805612	GGAGGTTGCATTTTC[A/G]GACCCTTAGGAGAGG	84182
rs779902290	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30843478	GCTTTTGAACTTCAC[C/T]GTGGGCTTCTGGGGG	84182
rs779907511	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30835438	TTATGGGAGTTACAA[A/C]ATGAAATTTGGGTGG	84182
rs779915498	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30843907	TGTGCCAGGTGCCAA[A/G]GAGCCAGACCTTATG	84182
rs779967870	snp	G/T	3.39518e-05	0.00412004	utr-variant-5-prime, intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30771453	GTTGCCTGGTGCTGC[G/T]GCCCGGCGTGGGCCT	84182
rs780007326	snp	A/G	3.31356e-05	0.00407022	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859311	TCTGCCATCCTGTCC[A/G]GGTCTACAGAGCTGT	84182
rs780032251	snp	A/G	1.65655e-05	0.00287793	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782048	TCACTTTGGAAATAC[A/G]GCTAACAATTTCACT	84182
rs780124818	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30814889	ACATGTGGCTCACAG[C/G]TCTTATATAAATGCT	84182
rs780173276	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30878302	TGGGGCCCTCACTGG[C/G]TATGTGGGAGGAGGA	84182
rs780178499	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30842473	CTGCCCTCAGAGGGT[A/G]CAGGGATACTGAGCA	84182
rs780203166	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30786447	AGGAGACACTTGTCC[C/T]ACCGCCCCATCTCTA	84182
rs780215006	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30827767	AGCTCTTCCATTCAC[A/G]CCCCTTCATACATCT	84182
rs780228888	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30802066	TGAGATAATATTTGG[A/G]AGATGAGTGTGAGAG	84182
rs780248980	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30779303	CATAAAGTGTTGTCC[A/G]ATGGCATAGTGAAAT	84182
rs780250120	in-del	-/TTTG			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828317	ATGACAAGAACTCGA[-/TTTG]TGTGTGTGTGTGTGT	84182
rs780264952	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853282	CTCTCTGACGCAGGG[A/G]CATTCCCAAGTTGGA	84182
rs780289944	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30858669	TATATATATATATAT[A/G]TAAATTTAAGACATG	84182
rs780291582	snp	A/C	2.01855e-05	0.00317685	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853448	ACTTTTCTTCAACAA[A/C]GCATTCATCAGGTAT	84182
rs780291607	snp	C/G/T	4.98371e-05	0.00499164	missense, stop-gained, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882262	ATCCTCTTTAGCCTG[C/G/T]AGCCGGGGCTCCTGC	84182
rs780292877	snp	A/G	1.67251e-05	0.00289176	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791525	AGGATGACCCAGGAG[A/G]GGCTGGAAAGAGCGT	84182
rs780297619	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852125	CACCTTCTTATTTGT[C/G]CTTATTTAATGACAC	84182
rs780304297	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30833377	TGTGTAGGCAAGCTT[A/C]TGTTTTTAAAAGCCA	84182
rs780304997	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30773641	TCTTGAGTCTGTGGC[A/T]CCACTCCTGCAGTGA	84182
rs780321526	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30804062	GGCTGGTTTTCTCAA[A/T]TGGTGGCTGAGGGAT	84182
rs780329937	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30822742	CAGGCTCCAGTGATC[C/T]TCCCACCTGAAGCCT	84182
rs780371987	in-del	-/CACACACC			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785295	ACACACACACACACA[-/CACACACC]CATTGGCACACCTGA	84182
rs780374166	snp	A/G	6.23111e-05	0.00558137	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30781945	TGAAGCTGTATATAA[A/G]TTAATGATTTTTTTT	84182
rs780402699	snp	A/G	1.65605e-05	0.0028775	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30891982	GCATCAGTGAACTGG[A/G]ACGGCTCAGACCCCA	84182
rs780405210	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30870444	TCACTCCCAGCTGGC[C/T]CCTTCCCAGGCCTGC	84182
rs780418809	snp	A/G	3.33139e-05	0.00408116	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30836771	GTAGCAAAGGTAAGT[A/G]TAAGGAGACTCCTGG	84182
rs780448928	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30853302	CCCAAGTTGGATTTT[G/T]TAGCTACTAAAGCCA	84182
rs780457940	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859746	GCAGCCCTGCAGTCG[C/T]GTGGACAAGGCTGGC	84182
rs780493964	in-del	-/GGACCGGT			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30789162	GGTGGACTACTCTGA[-/GGACCGGT]GGACCGGTGAACCAG	84182
rs780493989	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30802889	ACCATCCAACCATCC[A/T]TTCATCCAACAAACC	84182
rs780496963	snp	C/G	3.58108e-05	0.00423133	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791157	GCTTTTGTCCTTACT[C/G]CCTTTAGGATTCTTT	84182
rs780520896	snp	A/C	5.61183e-05	0.00529679	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850590	GTGTTGCCGTGGCTC[A/C]TCGTCTGCTGGCAGC	84182
rs780528499	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791855	GTCTTGTGCCACGCA[G/T]AAAATATACTAACAA	84182
rs780557492	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30855767	GAGGGGGCCTCCTTT[A/C]AGTGATGCCTCTGGA	84182
rs780582618	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30797996	GAGGCACTGAAGGAC[C/T]TGGGAGAGTTTGGGG	84182
rs780597493	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30809283	CATTCAATCTGTAGC[A/G]GCAACTGCTTAGCTA	84182
rs780597704	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30824372	AAAGCACTCATGACT[C/G]AATCATCTCCTGAAT	84182
rs780623137	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30885342	CTAACCAACATGGAG[A/G]CACCCCATCTCTATT	84182
rs780631647	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30886373	AACCCTGTTACCAGT[C/G]CAGGGAAAGATGCAC	84182
rs780642230	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30788638	ATACACTATTTGTTT[C/G]CCTTGAGGTGACAGG	84182
rs780649449	snp	C/T	1.65696e-05	0.00287828	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791246	GAGAGCCGGAAGGTC[C/T]CTGAGCTCTTTGTCT	84182
rs780652146	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30848300	GTATGTGCAATGGTG[A/T]TTGGACGGTGGGGTG	84182
rs780652445	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30818528	ATGAAGAATAAAGAA[C/T]AGATGAAGAATCTGA	84182
rs780660232	snp	G/T	1.66518e-05	0.00288542	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839220	AAAGACCCTTCTGTT[G/T]GGTTCCAGCTTTTGC	84182
rs780660274	in-del	-/GGG			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30871162	GTCATGTGCAGAAGT[-/GGG]GGGGACAGACCTGGG	84182
rs780669746	in-del	-/GTTTTT			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30847739	TGTTTGTTCGTTTTT[-/GTTTTT]GTTTTTGTTTTTGTT	84182
rs780680327	snp	C/T	1.65603e-05	0.00287747	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875498	TCTCATCTGCAGGAA[C/T]TTGTCAATCTGCTCC	84182
rs780701349	snp	A/G	1.656e-05	0.00287745	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30875557	CAACGATGTGGTTGA[A/G]CTGGATTCTGGGGAT	84182
rs780756536	snp	A/T	3.31318e-05	0.00406999	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852205	CTCATGCACCTTCCT[A/T]TCCTTTTTAGGGCTT	84182
rs780765906	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30776441	CTTTGATAAAGTAGC[A/G]GCGCATCCCCACACC	84182
rs780779892	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30830902	AATGGCCCTGTTGGG[A/G]AGGATGTGGGGGTCA	84182
rs780781515	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30845170	TCCATCGCTGGACAC[C/T]CACACAGACTCCTAG	84182
rs780827726	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30883949	TGATGCATACCTTTC[C/T]CACTGGACCTTGTGA	84182
rs780831913	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30777699	CACCCCTAACACCAG[A/G]CTGAGCTGTTGGTGA	84182
rs780841516	in-del	-/CTCATCAC	1.65627e-05	0.00287769	utr-variant-3-prime, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30892039	CCCTGTGGTCCACCA[-/CTCATCAC]CTCATCACCGAGGAT	84182
rs780854737	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30856746	TTGTGGCAGATTAGG[C/T]AGGCTTTCTATGGAA	84182
rs780873767	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30830074	GAAGTCTTGTGGGGG[C/T]CAGGGGGTTGGGGGT	84182
rs780874735	in-del	-/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30772756	TGACCTGCCATCACC[-/T]GTCCTGGCTGCATGT	84182
rs780883742	snp	A/G	3.31505e-05	0.00407113	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778399	GGGTTTTGATTTAAG[A/G]TGGTAAACAGCGATT	84182
rs780928695	snp	A/G	1.94759e-05	0.00312051	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859196	GGCTCCCACAGAGGT[A/G]TGGGGCTGGGAAGAG	84182
rs780928854	snp	C/T	2.2001e-05	0.00331663	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882408	CCTGTCCCCAAGGAG[C/T]CTCCAGGCTGGTCAC	84182
rs780945766	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30784032	TTTCTTCTGGTTCCA[C/T]TGAAAAGCACTTCCT	84182
rs780981862	snp	A/C	1.65663e-05	0.002878	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30859292	CTGCATCCTGCTCAC[A/C]CTTTCTGCCATCCTG	84182
rs780982020	in-del	-/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30881735	GGAGATGCAGGCTGT[-/C]CCAACGGTAAGCAAG	84182
rs780998922	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30796093	TTTATGCCTGCCACA[C/G]AGGGCAGCTGTTTGT	84182
rs781051919	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30818559	AGCCCAGAGAAGCTG[A/G]ACACTTGCCTCTCCT	84182
rs781115074	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30862207	TGAGTGGAGCTAACC[C/T]TCCTACCCCACCTGG	84182
rs781117205	in-del	-/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30831762	TCCCTATGGAATCTT[-/C]CTATGAACATCATTC	84182
rs781166574	snp	A/G	1.65608e-05	0.00287752	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785830	TAAGCCCATGCAGAC[A/G]GTCCCGGGTGAAACT	84182
rs781255248	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30793696	GGCAGGTATTCTCAT[A/G]TAATACATGGTGGGG	84182
rs781260989	snp	G/T	9.93739e-05	0.0070482	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828724	GGATGGTGAGCTGGG[G/T]GCCCTGCGGCTCGGT	84182
rs781315328	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30833110	CTGGGTAGACATCTG[A/G]TCTTTGTTTTAGGTT	84182
rs781316989	snp	C/T	0.000101566	0.00712549	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850403	GTAGAGCTGCACCAT[C/T]TCAACCTTGTGTCCA	84182
rs781322322	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30825434	TACCCAGTGGAAACA[G/T]TCCCACCATCTCAGC	84182
rs781326159	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30833725	CCAGTAAAATCAAAA[C/G]CAAGTTAGTTACTTC	84182
rs781329550	snp	A/G	1.65798e-05	0.00287917	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785763	GACATGACAATCTTG[A/G]TGGAGATGTACTTGG	84182
rs781350730	in-del	-/GTGC			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782370	TGTGTGTGTGTGTGT[-/GTGC]ATGTATCTATATGCA	84182
rs781355340	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30871533	ATACTGAATTGTTCT[C/G]GTTCCTAGCGGTGCT	84182
rs781436347	in-del	-/AGGGGGCCGAG	5.22071e-05	0.00510889	frameshift-variant, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30850526	CATTGTGTGGCGGGC[-/AGGGGGCCGAG]AGAGAGCCGTTGTTG	84182
rs781437002	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30826612	GGAGAGCCTTGCAGG[A/G]TACCTTCATGGGCCT	84182
rs781473616	snp	A/C	1.65674e-05	0.00287809	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30840801	TGTCCAAGGCTGTGT[A/C]CTACAGAAACTCCTG	84182
rs781484608	in-del	-/ACACACACA			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30785292	CACACACACACACAC[-/ACACACACA]CCCATTGGCACACCT	84182
rs781505488	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30873555	TGGGTCTGGGCTGGG[C/G]CCTAAGATTCTCAAT	84182
rs781514317	in-del	-/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30818250	TTTCTACTGTTAAAA[-/T]TAGTCTTGCATTTCT	84182
rs781515090	snp	A/T			missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839242	AGCTTTTGCTGTTTC[A/T]ATGAAGAATGGAAAC	84182
rs781526610	snp	A/G	9.94975e-05	0.00705258	missense, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30791391	ATCTGCCCAGCAAAC[A/G]GCTGCCCCCATGGGA	84182
rs781595669	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30872066	CTGGGCTCTAGCCCC[A/G]TCCCTTCTGGGTGGG	84182
rs781606316	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30849625	TGCCCCTCTGACCCT[G/T]CTTCCTCTGCCTCCG	84182
rs781607545	in-del	-/TT			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30828319	ACAAGAACTCGATTT[-/TT]GTGTGTGTGTGTGTG	84182
rs781669272	snp	C/T	4.97393e-05	0.0049867	synonymous-codon, nc-transcript-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882973	CCTTGTCCCACCCCT[C/T]GAGCTCTGCATCAGA	84182
rs781704238	snp	A/G	1.71897e-05	0.00293164	splice-acceptor-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30882180	CCTCTCCCTCATCCA[A/G]GTTGGCTGCTTCCTG	84182
rs781709082	snp	G/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30787536	GAGCAGGACACTGTT[G/T]TGTTTCTGTGTAGTG	84182
rs781714716	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30781406	TTAATTCCAAAACCT[A/G]CTACTGAAGACTTTC	84182
rs781715509	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30799574	GTTTCTCAGGTTAGG[A/T]TCCTAAGAACAATGG	84182
rs781730479	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30888065	TGTCTTGTCCTGGCT[C/G]ACACAGGCTCTATCA	84182
rs781737529	snp	C/T	1.65688e-05	0.00287821	intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30778582	GGTGTGGTGTGGAGT[C/T]TTGGAACTGAGTTTG	84182
rs781741920	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30839588	GCAGGTGCTGGGATC[C/T]TCAGCAGGAGAGAGA	84182
rs781745211	snp	C/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30837290	TCTGGGATTGCTCAC[C/G]ATGCTCGGCTACCAG	84182
rs781748670	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30876832	ATCCTCAGAACCAGG[A/G]CGCAGAGATTGACTC	84182
rs796096436	in-del	-/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30799966	GGCAAGGGAGTGAGC[-/T]TTTTGTGCCCCTCTT	84182
rs796116058	snp	A/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30776628	AGTGGTCTGTTCCCT[A/T]CGTTTCACAGATAGG	84182
rs796137442	in-del	-/TA			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30812283	TTGAGGGGGGGGGGG[-/TA]TGTATGTATGCATTG	84182
rs796152034	in-del	-/A			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30864414	AGTGTAAGCAGAAAC[-/A]AAGCTACTGACTGAT	84182
rs796252636	in-del	-/AG			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30789180	ACCGGTGAACCAGAG[-/AG]GAGCGCCAGGGTCCT	84182
rs796255941	in-del	-/TG			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30816300	CTGAGTCTGAGACTG[-/TG]GTAAATTTGTTCTCC	84182
rs796302649	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30793748	AGCCCACTTCTAAGA[A/G]GAAAAAGGGTAAAGC	84182
rs796328245	in-del	-/AG			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30812271	TGTGTATGTGTGTTG[-/AG]GGGGGGGGGGTATGT	84182
rs796336955	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30816561	CGAACAGCCTGGGCC[C/T]GATGGCTTTTCCAGG	84182
rs796371609	in-del	-/TT			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30796122	GTTGGAGCACTGTAC[-/TT]TTTTTTTTTTTGTCT	84182
rs796382854	snp	C/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30843027	ATATGGTTACCTGTC[C/T]ACATCTGCCGCCACC	84182
rs796384867	in-del	-/CTTCTTC			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30877677	CTTCTTCTTCTTCTT[-/CTTCTTC]TTTTTTTTTTTTTTT	84182
rs796552391	snp	A/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30837797	CACGTGGCCTCTGGA[A/C]AGCAGAGTCCAGGTT	84182
rs796573801	in-del	-/A			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30825565	AGGGGAAGGATGTGG[-/A]AAATAGAGGCAAGAC	84182
rs796623231	in-del	-/A			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30879944	TTAGTGATACAAAAA[-/A]TAATGGCGAATCTGA	84182
rs796649574	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30826462	GTGAGTTTGTTTGCC[A/G]GAGTATTCTAGATGG	84182
rs796677198	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30776349	GCTGTTCCTTGCCTG[A/G]AACACTTTTCTCCCA	84182
rs796688893	in-del	-/TG			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782371	GTGTGTGTGTGTGTG[-/TG]CATGTATCTATATGC	84182
rs796750727	multinucleotide-polymorphism	CA/TG			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30810974	CTTGGTTTATCTTCC[CA/TG]TTTTCTTTCCCTCAA	84182
rs796752924	in-del	-/T			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30852000	TCTTTTTTCCATTTC[-/T]TTTTTTTTTCTTTTA	84182
rs796851698	in-del	-/A			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30782712	TGTCTCTTAAAAAAG[-/A]AAAAAAAAAGTTTAT	84182
rs796869401	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30860270	TTGGGTCTGGTCGGC[A/G]CCCTCCCTGTTTCCA	84182
rs796879465	in-del	-/C			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30885706	TAAGGGCAGTGCCCA[-/C]CCCCCCCCCCAACCC	84182
rs796953321	snp	A/G			intron-variant	FAM188B, INMT-FAM188B	GRCh38.p7	7:30795445	TTCAACCATGGAGCC[A/G]TGGGATCCAGGGGTA	84182

Page 1 | 2