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

MINDY3

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs181941452	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15853618	AAAAATATATTCTGC[A/G]GAACAAAATGGAAGC	80013
rs181941533	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15818964	AATTGTATGCTTTAA[A/G]ATGGTGAATCTCCTG	80013
rs181946273	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15803669	AGGCTTAATAGATGG[C/T]AGAGAAAAACCCAGT	80013
rs181947156	snp	A/G	0.0023933	0.0345097	intron-variant	FAM188A	GRCh38.p7	10:15840018	TATTTCATAGTATGC[A/G]CTCAGTATACTGTTA	80013
rs181948727	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15824034	TCCATTGACCTGTTG[A/G]TGGACACTTAGGTTG	80013
rs182112198	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15854758	GGACACAATTTTCTC[C/T]AGCAATACACAGCAG	80013
rs182118735	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	FAM188A	GRCh38.p7	10:15778466	CTTTTTGTGAACATG[A/C]CAGAGTTAAGTAAAT	80013
rs182134453	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15848191	TCCTCTAGGAGGATA[A/G]AGTATGGACTTTAGT	80013
rs182162008	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15854994	AGTGCAGAGGCAAAA[C/T]TAAGATCTGCTAAAC	80013
rs182179483	snp	C/T	0.00478085	0.0486577	intron-variant	FAM188A	GRCh38.p7	10:15825703	AATTAAAGTTGTATA[C/T]ATTTACCGTGTACAA	80013
rs182182492	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15841983	TGTTGAAACCTCTAT[C/T]TTTTTTCCCTCACAT	80013
rs182194671	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15810882	AATTAAAAAACAGGC[A/G]AAGGACCTGAACAGA	80013
rs182199584	snp	C/T	0.0023933	0.0345097	intron-variant	FAM188A	GRCh38.p7	10:15795457	ACTTCCATTTCTACA[C/T]GGTACTTCGTAAGGG	80013
rs182284513	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15851633	ATCCCATCTCCAGTC[C/T]ACCCTATAGTTCAAA	80013
rs182287447	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15794736	AGAAAATAAATAGTA[A/C]AAGCCTGCTACCTCA	80013
rs182300461	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15837928	CTACTAGAAATCTTC[A/G]TATTTGTTTAGGTCA	80013
rs182305869	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15822506	CAGGTATGAAAAATC[A/G]ATGCATTTAAGGAAT	80013
rs182307502	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15807091	TGCAGATGAAAACGG[C/T]ACGCAGCTCACAGGG	80013
rs182318550	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15791984	AAACTAACAGAGAAG[C/G]TGGAAAAAGGTTTCT	80013
rs182400536	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15833395	CACAGAAAATGAAAG[G/T]CCTGAGAAGTAACTT	80013
rs182431197	snp	A/T	0.00676609	0.0577691	intron-variant	FAM188A	GRCh38.p7	10:15809143	TTATTCTTAAAACCC[A/T]AGTATAAAAATAAAA	80013
rs182539293	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15804411	ACACCTACTGAAATA[A/T]AAGGCCTGTGTACAG	80013
rs182657781	snp	C/T	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15848550	GAGGCCGAAGAATGG[C/T]GTGAACCTAGCAGGC	80013
rs182682418	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15799486	ACAGGCTTGAGCCAC[G/T]GCAACCAGCCTTTAA	80013
rs182735595	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15845912	ACTGCAACCTCCACC[C/T]TCTGGTTTCAAGTGA	80013
rs182735826	snp	A/T	0.00159617	0.0282053	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15861691	TTCAAAAACATGCAG[A/T]TTCATTGTAGAATAC	80013
rs182741874	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15852295	GGCATGGAAGATAAT[A/G]GCAGTGTTTGTTTCT	80013
rs182744313	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15830402	GATGAGAAAGAGGCA[C/T]TGAGTGAAGCATCTT	80013
rs182747597	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15838818	AGTAACTTATTTAGA[C/T]TATGTTTATTAATCA	80013
rs182755381	snp	C/T	6.72687e-05	0.00579912	intron-variant	FAM188A	GRCh38.p7	10:15816790	ACTTATAATACTTGT[C/T]TGCCTGATGTCATAA	80013
rs182800054	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15819775	GTGCCATTAGCAGAA[C/G]CCTTAAATCTCATTT	80013
rs182826697	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15787061	ATACAGGGTCAAAAG[A/G]CAGTGGTACATCAGA	80013
rs182828517	snp	C/G	0.0170251	0.090679	intron-variant	FAM188A	GRCh38.p7	10:15788256	CTAGTTCAACACTCT[C/G]AATTTCTCTTTAAAT	80013
rs182999829	snp	A/G	0.00478085	0.0486577	intron-variant	FAM188A	GRCh38.p7	10:15829510	ACTGGATTTGTGAAG[A/G]AGACTAGTAAAAGAT	80013
rs183014358	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15822203	ACATTTAATGCCATC[C/T]CTCTTTCCTATAAAC	80013
rs183020877	snp	A/G	0.00557542	0.0525036	intron-variant	FAM188A	GRCh38.p7	10:15799280	TCTTGCCTCACTGCA[A/G]CCTCCACCTCCCAGG	80013
rs183022964	snp	G/T	0.00318978	0.0398085	intron-variant	FAM188A	GRCh38.p7	10:15791313	AAGTGTAAAAACAGA[G/T]GAAACCTAGGTCATC	80013
rs183031637	snp	C/T			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15782725	ATATTTGAATATTGT[C/T]AACCATTAATTAGTG	80013
rs183102451	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15850617	TCCTGCCTAGTAAAT[C/T]TTAGTCAGACCGGTT	80013
rs183135059	snp	A/G	0.00795532	0.062565	intron-variant	FAM188A	GRCh38.p7	10:15848406	TTGGGAGGCAGAGGC[A/G]GGCGGATCACGAGGT	80013
rs183152676	snp	C/T	0.00199481	0.0315187	intron-variant	FAM188A	GRCh38.p7	10:15796970	TGTCTTTGCCTATAA[C/T]GGTGTTTACTCAGAC	80013
rs183152830	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15833863	CAATTTTATATATTC[A/G]GCCTTGCTAAATGTA	80013
rs183158099	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15819349	TGTAGCGTAATATAG[G/T]TTTTCAAAAAATGCT	80013
rs183159474	snp	A/T	0.00953873	0.0683987	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15779368	GGCCAGGTGATTTTT[A/T]AAAAATTCAAGATCA	80013
rs183161089	snp	G/T	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15803976	TGGAACTCTTTTAGG[G/T]ACCCTCAGTAGGAAG	80013
rs183258801	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15859195	TGTGGGAGGGAGGGA[C/G]AGATTACGTAAATCC	80013
rs183282250	snp	G/T			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15783166	TTTAGAGACAGGGGA[G/T]GGGAGGTGGAGACCT	80013
rs183286888	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15806828	AACACTACATCTATA[C/G]AGCTTTCACTTCATA	80013
rs183352312	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15842193	TGAACCTTAGCCACA[C/T]TCTTTTCAAGCAGTA	80013
rs183354012	snp	A/G/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15855475	GTTTTTCCTGATTAC[A/G/T]TCTGAAATTACCCAT	80013
rs183360326	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15836954	TCAAAGGAAACACAA[C/T]TTGGAAGAAAGGACA	80013
rs183400348	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15785924	ATAAAATGACCATGA[C/T]ATCTGTTATCTAGTT	80013
rs183403639	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15830176	TGTTTCAATTTTCTA[C/T]AAAGGGCAGTTACAA	80013
rs183505242	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15823183	TAAATCCAAAATTAA[C/T]AGAAGGTGCATATAC	80013
rs183537973	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15842752	CACACATCTCTCTGG[A/G]TACAGAAGCTCATGT	80013
rs183563381	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15812881	ACATTTCTACCCCTC[C/T]GCTGCCAATCCAATC	80013
rs183620495	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15856733	GCTAAGCAATCAATA[C/T]TGAAAAGAAAATAAA	80013
rs183626794	snp	C/T	0.0379877	0.132479	intron-variant	FAM188A	GRCh38.p7	10:15845809	ACCGTGCCTGGCCTA[C/T]GTGATTTTTTTTTTT	80013
rs183629635	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15843409	AAAGATGTCAAATGG[C/G]TTCCCCTCACATTTG	80013
rs183631664	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15827823	AAGCTCAGGCTCAAT[A/G]AGCACCAGAGAAATG	80013
rs183649600	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15813919	GAACTGCTGGGGAAA[A/T]ATTAAAACAATGTTG	80013
rs183697756	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15815688	GATGATGATGATGAC[G/T]ATGACCACAGCTAAA	80013
rs183711073	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15782493	TTTTTTTTTTAATTA[C/T]GTGCATGTATCACTA	80013
rs183742641	snp	G/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15797430	CATTTCCAACATTAT[G/T]TTGCTGATAATGTAT	80013
rs183746259	snp	C/G	0.00199481	0.0315187	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15779971	GGACATTAAGGCACT[C/G]CTTGGTGGTTAATTT	80013
rs183782225	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15827370	AACATGGTAAAATCC[C/T]GTCTCTACTAAAGAT	80013
rs183853055	snp	C/T	0.0162398	0.0886349	intron-variant	FAM188A	GRCh38.p7	10:15856213	AAATAAATACCCAAA[C/T]ACGCCTTTAAACCTT	80013
rs183888095	snp	A/G	0.00438332	0.0466095	intron-variant	FAM188A	GRCh38.p7	10:15793830	TTCAGAAATCGTAAC[A/G]TTCCACGCAAATGCC	80013
rs183888910	snp	A/C/G	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15796346	GGCCATTTATTTTAC[A/C/G]TCTGAAAAGTGGCAA	80013
rs183910602	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15798975	ACATGTGTTCATTTA[C/G]AGCAGGGTTTGGCAA	80013
rs183917640	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15862363	ATTTACGTAATTCTT[C/T]CACTTCCTGAAAGAC	80013
rs183940953	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15832898	TCAATTATATTTGCT[C/G]TGTTTGACTGTGAGC	80013
rs183961682	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15839884	TACTAAAATGTTTTC[C/T]GGAGGGTAATTCAAT	80013
rs183967097	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15823499	AAAATTTAAAACAAC[A/G]TCACTCTCCTTAATT	80013
rs183970538	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15808816	TAAAACTCATCTCCC[A/C]AACTTCAATGAAGAG	80013
rs183991861	snp	A/C	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15826545	CCAATCCAAATCTTC[A/C]AAGATTTCTTAAAAC	80013
rs184034049	snp	A/C	0.00755907	0.0610114	intron-variant	FAM188A	GRCh38.p7	10:15818336	AAAAAAAAACAAACA[A/C]ACAAAGGATAAGATC	80013
rs184053480	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15811613	TAAATCATGAAAAAT[G/T]AATAGAACTCAAAAC	80013
rs184067657	snp	C/G	0.000798403	0.0199641	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	FAM188A	GRCh38.p7	10:15778816	TAGGATAATCTTTAA[C/G]ATAAAGCTTTAGGAC	80013
rs184133129	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15805412	AGAATAGTTATACTG[A/G]TAATACAGATAGAGG	80013
rs184182896	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15832106	TTCTGGTTTGGGGAC[C/T]AGGGTAAGCTATCGA	80013
rs184197878	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15817899	ACTCTTTTGTATCCA[C/T]GGACAGAGAAACTAG	80013
rs184203612	snp	C/G	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15800890	GGTTGCTATAGGAAA[C/G]GCACACCTTTAGATT	80013
rs184208470	snp	G/T	0.00199481	0.0315187	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15784868	AAGGGGACATCAGTG[G/T]TATGTAGGGCATGAT	80013
rs184254305	snp	A/T	0.00755907	0.0610114	intron-variant	FAM188A	GRCh38.p7	10:15849375	GACAAGTGGTTAATA[A/T]TGCAAAGGGCCAAAG	80013
rs184257079	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15793079	GAGAATTGTTGTTGT[C/T]CAGTATCTTTGATCA	80013
rs184282347	snp	C/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15790017	TTCCTTAAATGTACA[C/G]TGCCCAATTTTCCCT	80013
rs184454801	snp	C/T	0.00318978	0.0398085	intron-variant	FAM188A	GRCh38.p7	10:15817057	CGAGCACTTCACCCA[C/T]AGAGATCAAATGCTG	80013
rs184492019	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15849231	AATTCAGCTAAAGAA[A/G]ATACCTTAATTAAAG	80013
rs184509508	snp	C/T	0.0023933	0.0345097	intron-variant	FAM188A	GRCh38.p7	10:15820748	AAAGAGGATCAACCA[C/T]GATTATCGTTATTAC	80013
rs184511725	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15835233	CAGAAGGGCACTCAA[C/T]TCCCAAAAGTTCTAC	80013
rs184539029	snp	G/T	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15846647	ATATATTTTTAATAA[G/T]GTAAGTATTATTATG	80013
rs184588675	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15831443	AAAATGCAAGAAATA[C/T]ACCCAATTTTCTTTT	80013
rs184605075	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15800190	AAAAAATTAAGTATG[C/T]CATGCATGCATAAAA	80013
rs184662445	snp	C/T	0.00159617	0.0282053	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15861933	TCCTTTTGATCTTTA[C/T]TCCCTTTAGAATATC	80013
rs184688959	snp	C/T	0.00716266	0.059414	intron-variant	FAM188A	GRCh38.p7	10:15853031	GCAAATACTGCAGAG[C/T]GTCTATGGATTTTGG	80013
rs184762497	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15834985	CTGATTTTTTTAGAT[C/G]ATGTAAAAACTTATT	80013
rs184769899	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15820499	GGATCTACGAATGTG[C/T]GTGTATATGTGTTAG	80013
rs184783188	snp	C/T	0.00318978	0.0398085	intron-variant	FAM188A	GRCh38.p7	10:15804717	CCTTTAGTCTTTGCT[C/T]ACTATCTGTATTTAT	80013
rs184789089	snp	C/G	0.00795532	0.062565	intron-variant	FAM188A	GRCh38.p7	10:15788921	ACAGAACCGTCATTA[C/G]TTTACTGAAGATACT	80013
rs184832564	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15801084	TAACAAAGAGGCAGC[A/G]GTTAAGTTCTCAGAA	80013
rs184837571	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15823263	AGCAATGGTTCTTCA[A/G]TTGTGGTTTAGGATT	80013
rs184862836	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15857324	ATCTCATCTTAAAAT[A/G]AGGCCTGACCAGGAC	80013
rs184882550	snp	A/C	0.00279162	0.0372561	intron-variant	FAM188A	GRCh38.p7	10:15815487	ACTTTCTACAGAAAC[A/C]AATAATAAACTTTCA	80013
rs184896091	snp	A/T	0.030665	0.119967	intron-variant	FAM188A	GRCh38.p7	10:15798800	CAAACAAACAAACAA[A/T]AAACCACTATGCCAA	80013
rs184936931	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15839684	GAATAAAGGAAAGAA[C/T]AGGTAAAATAGATTG	80013
rs184960851	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15844802	CCCACCCTTACATGC[A/G]CTGGCAATTGTAATT	80013
rs184963569	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15808372	GTGAATTTTCTTGGA[A/C]GAGTAAACGTATAAA	80013
rs184968752	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15858304	ATGGAACTAATCCTG[C/T]TAAAGAATTTCTGCA	80013
rs184979649	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15829230	GGAGTTAACATTTTA[A/T]TGGGGCCAGATGGAA	80013
rs184983988	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15862222	GGATCTCAATAATTA[C/T]GATTCCAAGGAACAA	80013
rs185101254	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15847056	CCAATGAATAATAAA[C/T]GCCACATTAAATATA	80013
rs185112800	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15855030	GTGTATGAAATTAAA[A/G]TGTGAATTAGTAATG	80013
rs185122036	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15807414	AAGACTTTGATAAGC[A/G]TATTCTGGGCAGAGG	80013
rs185123199	snp	A/G	0.00557542	0.0525036	intron-variant	FAM188A	GRCh38.p7	10:15826225	GGGAAGCCAGCCATC[A/G]AATGGTTTTAAGGGA	80013
rs185124977	snp	C/T	0.00279162	0.0372561	intron-variant	FAM188A	GRCh38.p7	10:15841989	AACCTCTATTTTTTT[C/T]CCCTCACATCTGAAT	80013
rs185229411	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15810923	AAGAACGTCTAGAAG[C/T]GGACAACAATCACAT	80013
rs185231940	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15795466	TCTACACGGTACTTC[A/G]TAAGGGAACTCTGAA	80013
rs185247389	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15792587	AGAATGCCTAGGGAG[C/T]GGTGTATATTAAGCT	80013
rs185396998	snp	G/T	0.00398564	0.0444627	intron-variant	FAM188A	GRCh38.p7	10:15805209	GACGACGTTCTTGGA[G/T]GTTCTTTGATTATTC	80013
rs185402046	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15810514	CCTCCATGTAAGATA[C/G]AGATCTATTGAATTC	80013
rs185414644	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15795354	AGAGGAAAAGAGCAG[A/G]TCACTAAGTGTACAA	80013
rs185528232	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	FAM188A	GRCh38.p7	10:15778277	TTTATCGTGTTTATA[A/T]ATATAGAAGAAAGCT	80013
rs185604031	snp	G/T	0	0	intron-variant	FAM188A	GRCh38.p7	10:15828285	AAAACATGGTCACCT[G/T]GAAAATATTATACTA	80013
rs185608905	snp	C/T	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15848814	AGAACCCAGTGACCA[C/T]CTGGATAACCCTGTG	80013
rs185622460	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15797864	AGTTGCAGATTTCTA[C/T]ATTTATTCTAGTATA	80013
rs185627161	snp	A/G	0.0023933	0.0345097	intron-variant	FAM188A	GRCh38.p7	10:15844185	ACAGTACCTGGCACC[A/G]ATAAACAATTCAAGG	80013
rs185752342	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15814460	ATTCAACTAATAATT[A/C]CCCCCACCCCTAGTG	80013
rs185768835	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15781635	ACTAAGTTTCACTCC[C/T]AGCTCTGTCATTTCC	80013
rs185779128	snp	C/T	0.00405401	0.0448394	intron-variant, downstream-variant-500B	FAM188A	GRCh38.p7	10:15782276	TATATTTATATCAGG[C/T]AATTTCTAATCAACT	80013
rs185821019	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15837095	ACGTAAAAGATTTTT[A/C]TTCTAAGAATTTAAA	80013
rs185900612	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15803775	AAATTTATCCTAAGA[A/C]AATTATCTTCCAAGA	80013
rs185908600	snp	C/T			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15786412	TCGAACACACATTCC[C/T]TCTGTCTGGGAAGGT	80013
rs185955324	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15850663	CTGTCTCCTGATAAG[A/G]TGTTATCAATGACAA	80013
rs185962835	snp	C/G	0.000798403	0.0199641	intron-variant, downstream-variant-500B	FAM188A	GRCh38.p7	10:15782006	CTGGTCAAATCCAAA[C/G]ATGGCTGATTCTAAA	80013
rs185963740	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15848292	AACTCTTTAAATACC[A/G]TATCATTCTATCATT	80013
rs185974010	snp	G/T	0.000149577	0.00864675	intron-variant	FAM188A	GRCh38.p7	10:15833601	ATATTATTCATCAAA[G/T]AGAGCAACATAACAA	80013
rs185984174	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15819063	TTGTTGGGTTTGTAC[A/G]TGTGTGTTGAGAGGG	80013
rs185990354	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15854012	TATGGTATAATGACA[C/T]ACACTAACACTTGGA	80013
rs186046784	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15814921	CGACACTGTTCCTTG[C/T]ATTATACCTTCTGTG	80013
rs186050905	snp	C/T	0.00318978	0.0398085	intron-variant	FAM188A	GRCh38.p7	10:15798444	TAAACTACCTGATGC[C/T]TTGTCTCTAAGTGCC	80013
rs186112909	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15847777	TATGTCTCATAATTA[C/T]TATATGGAGTACAGA	80013
rs186123432	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15818866	CTAATGGGTTTAGAG[C/T]TCCTTTTGTGGGTAA	80013
rs186140292	snp	C/T	0.00716266	0.059414	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15785793	ATTTTGAAATTTTCC[C/T]TCTTGCTTTTAAATT	80013
rs186140864	snp	C/G	0.0111196	0.0737302	intron-variant	FAM188A	GRCh38.p7	10:15850390	GGGAGCTGGGCAGAA[C/G]AGAGTCATATTTCTC	80013
rs186247839	snp	A/C	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15836576	CAACTGAGACTAACA[A/C]GTTACTAGAGCTATG	80013
rs186254875	snp	A/T	0.00835141	0.0640778	intron-variant	FAM188A	GRCh38.p7	10:15833352	CTGTGTTTATACATA[A/T]TAAGAGTCATAAATC	80013
rs186258136	snp	C/G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15854937	ACTGTTTGGCCAGCT[C/G/T]TTCTACTGAGAATAA	80013
rs186261902	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15802613	TTAAGGCAACTTATT[A/G]GCTGAAGTTAAGTGT	80013
rs186279216	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15825251	TGAGGAAAAATGCAA[A/G]TATTTCCAAATCTGA	80013
rs186371729	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15849935	CTTAACCCTCACTAA[C/T]CTGGTTTTCAACCCA	80013
rs186389805	snp	A/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15836151	CTGGTGTCTTATGCT[A/T]CAGTAAGGCTCAACT	80013
rs186391230	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15821939	GTGGGTAAATGTGAT[A/G]CTTTAGATGTATATT	80013
rs186396180	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15805868	CAACATGTAAGTTAT[C/G]AGGGCGGTAAGCTTT	80013
rs186425844	snp	C/T	6.61365e-05	0.00575012	utr-variant-5-prime, missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15841498	CCTCAGTTGTCTTTC[C/T]TCTTAACCATGAAAC	80013
rs186484241	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15790633	GTTTCTGTGTTTATA[A/G]GCTATATCCATTTGA	80013
rs186546715	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15809541	TTCTGCCACAGCTCA[C/G]ATGACCTGCTTGGAA	80013
rs186569971	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15791889	AGAAATAAACAGGAG[A/G]GCCTAGCAGGTCTCA	80013
rs186574477	snp	C/T	0.000798403	0.0199641	downstream-variant-500B	FAM188A	GRCh38.p7	10:15777782	CTATACTATTGAAGG[C/T]AATGTTCAGTTCTGA	80013
rs186626315	snp	A/C			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15785455	TAAGAATCAACATTT[A/C]TATCAAAAGTTCCGA	80013
rs186643180	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15840872	TAGCTATTATTTAAC[A/G]TAAACAGCTATTATT	80013
rs186659713	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15830443	ACACAGTTTAATAAA[C/T]GGCGCAACTGAGATT	80013
rs186662806	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15816978	ATACTGCCTCTTATT[C/T]GCCCATAAATATCTG	80013
rs186778207	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15824223	TTTTCCATAGTGGCT[A/G]TACAAGTTTATATTC	80013
rs186787111	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15788450	ACCAAATTCTAAAAA[C/T]GGTGTCTACCAATGT	80013
rs186794984	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15795042	CTTCACTAGTAAAAC[A/G]AAACACAACACAACA	80013
rs186908968	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15799296	CCTCCACCTCCCAGG[C/T]TCAAGCAAATCTCTG	80013
rs186937702	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15822156	TATCATTAGGTAGCA[G/T]TGACTCCACTTGCCT	80013
rs186951174	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15844478	GGTATATGAATGTAT[C/T]TTCTGTTTTTCTACA	80013
rs187075074	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15797072	GTTAACATCTAAACT[C/G]CTGTTCCCCTGTGAA	80013
rs187082374	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15833879	GCCTTGCTAAATGTA[C/T]CACCAAATATATCAG	80013
rs187084832	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15779691	AATATTCCTGAAATG[C/G]AATTCATGAGTGCAT	80013
rs187119968	snp	A/T	0.00199481	0.0315187	intron-variant	FAM188A	GRCh38.p7	10:15829533	TAAAAGATTATAAAC[A/T]TAGGGTTGAGTACGA	80013
rs187130640	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15799008	ATTTTTCTGTAATGG[A/G]CCACAGAGTAAATTT	80013
rs187145302	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15848410	GAGGCAGAGGCGGGC[A/G]GATCACGAGGTCAGG	80013
rs187153977	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15828573	TATCTCAATAAAGCT[A/G]TAAGTAAAAAAAAAA	80013
rs187170832	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15827497	GCAGTGAGCCAGGAT[C/T]GTGCCACTGCACTCC	80013
rs187172468	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15813150	CAAAACTACTCCCAC[C/T]ACCAATTTTTAACAA	80013
rs187175093	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15858796	GTTAACTGATTACAA[C/T]GGAAGTAAATTTTTT	80013
rs187249575	snp	A/G	0.00517822	0.0506191	intron-variant	FAM188A	GRCh38.p7	10:15820592	ACAATTAAAGTCACC[A/G]AAGATAAAAGTCACT	80013
rs187255427	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15804920	CAGGTCACCTCCACA[A/G]TAGCCCACTGCTGTG	80013
rs187263150	snp	C/T	0.00279162	0.0372561	intron-variant	FAM188A	GRCh38.p7	10:15789182	AAGGCAAAAAATGTA[C/T]AATATGTCTTAAACT	80013
rs187271462	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15845494	TCTTTACAAAGTTTA[C/T]GTGACTCTTTTTTTT	80013
rs187305720	snp	C/G	0.00557542	0.0525036	intron-variant	FAM188A	GRCh38.p7	10:15846100	AGTGCTGGGATTACA[C/G]GCATGAGCCACCACG	80013
rs187308225	snp	G/T	0.0263992	0.111815	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15861749	CCTTAATTTAAAATC[G/T]TTTAGATTGCAAATA	80013
rs187506186	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15783544	CTGTAAAGTTTTTCC[C/T]GGACACACTAGTTAG	80013
rs187512502	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15806955	GTTGTTTTCTTAAGG[A/G]AGGGAAGTAGTTAAA	80013
rs187537699	snp	C/T	0.0158469	0.0875917	intron-variant	FAM188A	GRCh38.p7	10:15830272	TGATAAGAGTGCTCA[C/T]TATGCAGCAGTGGCA	80013
rs187540671	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15845860	CAGAGTTTCACTCTT[C/T]CACCCGAGCTAGAGT	80013
rs187551703	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15816684	AGCACGAAAACAGTA[C/T]GTTCTTCAGTATTAG	80013
rs187610112	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15848615	CTCCAGCTTGGGCCA[C/T]AGAGCTAGACTTCAT	80013
rs187625532	snp	G/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15820293	GCGTGTCTGGGAAAG[G/T]GAGAGGACCAGTGTG	80013
rs187641884	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15799317	CAAATCTCTGCCCCA[A/G]CCTCCCTAGTAGCTG	80013
rs187654592	snp	G/T	0.00398564	0.0444627	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15782838	TATATCACTAACAGA[G/T]TAAGCTTGTAGAAAA	80013
rs187658130	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15823105	AACATTTTACTGTGT[A/G]GCCTTAACTACAACA	80013
rs187679952	snp	A/G	0.00398564	0.0444627	intron-variant	FAM188A	GRCh38.p7	10:15807274	GTGTGACAGTAGGTA[A/G]TGTGGGAAATCAGTT	80013
rs187683835	snp	A/C	0.00199481	0.0315187	intron-variant	FAM188A	GRCh38.p7	10:15792220	CACACACCAGAGCTG[A/C]GCTTTTCCAGACCTC	80013
rs187739347	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15851692	TTGAGTTTCCAACCA[C/T]GTCTCCCTATTCCTT	80013
rs187745680	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15800008	AAGAAGCGAGTACAG[C/T]TGATCCTCAAACAAC	80013
rs187750615	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15822350	TACACACACACACAC[A/G]GAGTGGTATGAGAGT	80013
rs187755366	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15838150	ATGTAAAACTAAGAA[C/T]CTTTCCACAGTATGA	80013
rs187883529	snp	C/T	0.00158013	0.0280637	missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15834613	TTTTTATGTTTTCAA[C/T]GCCCTAAAGAAACAG	80013
rs187884344	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15849096	GAATAAACTAATGTT[A/G]TAAGAGAAGAATGCA	80013
rs187892834	snp	A/T	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15835048	GAGATATAACATTAA[A/T]TAATTTGCGTTTTAA	80013
rs187904185	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15804416	TACTGAAATATAAGG[A/C]CTGTGTACAGTGGGT	80013
rs187905623	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15804026	CAACGATTACATACT[A/G]TTTTAGTTAGCAATT	80013
rs187943878	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15856313	TAAGTTATTTGTTAA[A/G]TATCTTTTTTTCATA	80013
rs188038464	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	FAM188A	GRCh38.p7	10:15778580	TTTCATTGTAGAGGC[G/T]GATATATTACAAGCC	80013
rs188147826	snp	C/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15793249	GGAACACTTTGAATA[C/G]ACCTGATAACTGCTT	80013
rs188182025	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15819602	GCTGACCCCATCCTA[C/T]TTCAGGTACATCAGC	80013
rs188194055	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15787791	ATATGGCATTTTAAT[C/G]AGTCTGAGTAAGGCC	80013
rs188229618	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15842284	TTTCTGTCTCTCCTA[A/C]TGGATTAACAGTTCT	80013
rs188247594	snp	C/T	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15842973	TTCTAGGAAATGCAC[C/T]GTGTTTTACCAAGAG	80013
rs188257613	snp	A/T	0.00478085	0.0486577	intron-variant	FAM188A	GRCh38.p7	10:15811941	TTTTTTAAATTTTTT[A/T]ATTATTTTTATTTTT	80013
rs188292246	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15805465	CTTTATTTCAAAGTT[A/G]GGACTCTTTGTATCA	80013
rs188296468	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15828121	TAAAATATACATCTC[A/C]TAAAAACTTGTACAT	80013
rs188297829	snp	C/T	0.00636936	0.0560724	intron-variant	FAM188A	GRCh38.p7	10:15790083	TAAATCAGCTTCCAA[C/T]GTCCTTCAGGGATTA	80013
rs188374850	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15843929	TTTAAATTGCAGTTT[A/C]TTGGGCTCCACCTAT	80013
rs188382812	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15856924	GACTGCTGCCATTGT[C/G]TCTTATCTGATCTTG	80013
rs188393816	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15829071	AAGCCTAGGCACCTC[A/G]TTTACAGAAGCAAGA	80013
rs188395582	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15844635	GCTCCTTTTTAAATA[C/T]AACTTTTTCCATATT	80013
rs188398440	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15823235	TAGCTTCTTACAGGC[A/G]CAGATCAGGTAGAGC	80013
rs188416525	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15792823	TGTGAAAACCTGTGA[C/T]TAGCAGTTCAGACAC	80013
rs188506619	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15849272	TTCCAAGAGGACAGA[A/T]TGTTTATAAATCAGA	80013
rs188508599	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15815242	CTCTACTTCAGGAAG[A/G]AAATAAATAGCAAAA	80013
rs188508765	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15798515	GGGCACGGTGTGTCA[C/T]GCCTGTAATCCCAGG	80013
rs188521772	snp	A/G	0.00636936	0.0560724	intron-variant	FAM188A	GRCh38.p7	10:15855705	ACTATACCTTCTACA[A/G]TTCTAGCCTTCCATG	80013
rs188522968	snp	C/T	0.00318978	0.0398085	intron-variant, downstream-variant-500B	FAM188A	GRCh38.p7	10:15782074	TAGGTAGCAATTGTA[C/T]GGGAATCGAACATTG	80013
rs188525868	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15826756	AAACATGTAAATATG[C/G]AAAAATGTGTTCAAC	80013
rs188544973	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15796903	ACTTGACACACATGA[A/G]TCTAAAATGTAGGCT	80013
rs188643785	snp	G/T	0.00318978	0.0398085	intron-variant	FAM188A	GRCh38.p7	10:15847498	TTAGGAAAGTAACTT[G/T]TACAGACTGAAATAA	80013
rs188664454	snp	C/T	0.00279162	0.0372561	intron-variant	FAM188A	GRCh38.p7	10:15838914	CCCTTTTCTAAATGC[C/T]CTACATGTCTTACCT	80013
rs188682052	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15860730	AATACCTTCTTCCTC[C/T]ACGCACTGCTCTGGG	80013
rs188684510	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15807497	TTAGTAAGACTTAGT[A/G]GCGGTCATCTATTAA	80013
rs188726140	snp	C/T			upstream-variant-2KB	FAM188A	GRCh38.p7	10:15861965	CTTGCCTTGTTTTTG[C/T]AAATCAAATCTTACC	80013
rs188757036	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15832088	TAGGGAGGCAGAAGA[C/G]TATTCTGGTTTGGGG	80013
rs188814533	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15823298	AGGGACCACAAGACC[C/T]TCTTAGAGACTACGT	80013
rs188820089	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15808563	TAGAAATAATTCTCC[C/G]TACATTCCCAGTAAC	80013
rs188938702	snp	C/T	0.00517822	0.0506191	intron-variant	FAM188A	GRCh38.p7	10:15818211	GTTTTCTGACTTCTA[C/T]CTACTCTGATGGATT	80013
rs188953833	snp	A/G	0.00478085	0.0486577	intron-variant	FAM188A	GRCh38.p7	10:15801003	TGCCAGCAAAGGATG[A/G]TTTGATAATTTTAGA	80013
rs188962355	snp	A/T	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15785191	GAACTATACAGACAA[A/T]GAGACAAACCAGGCC	80013
rs189022212	snp	C/G	0.00835141	0.0640778	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15862291	CAGCAAGTGAGAGAT[C/G]GGGGAAGTAGTACTG	80013
rs189025720	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15832343	GGGGTCCAGAAACAA[C/T]TGGAAGAAGAAGAAA	80013
rs189028049	snp	C/T	0.00438332	0.0466095	intron-variant	FAM188A	GRCh38.p7	10:15846708	AATTTACTTTGTAGC[C/T]AACAGTTTAGGAATG	80013
rs189030025	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15847277	CAATGTAACATACCA[A/G]GATTCCAAATCAAAT	80013
rs189038952	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15817209	TCAGGTTTTGCTAAA[C/G]TTCCTAGATAAAATG	80013
rs189201462	snp	C/T	0.00279162	0.0372561	intron-variant	FAM188A	GRCh38.p7	10:15797435	CCAACATTATTTTGC[C/T]GATAATGTATACGCC	80013
rs189255187	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15849724	AGAGAGGGTGCCATT[A/C]CATCCCATCTCCTCT	80013
rs189261177	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15821418	ATTATTTTGTACTGG[A/G]TTCTGCCCCTCCTCC	80013
rs189315146	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15853556	TTACTGCTGCAGTCA[A/C]AATTACTAATTTTAT	80013
rs189400126	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	FAM188A	GRCh38.p7	10:15857949	GACTGCAGTTGTCAA[C/T]TGAAGACACGATCAC	80013
rs189425138	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15824007	ATTGTTTATAGAATT[C/T]CAGTTTCTTTATCCA	80013
rs189426630	snp	A/T	0.00636936	0.0560724	intron-variant	FAM188A	GRCh38.p7	10:15839917	AATATGCCCATCTAA[A/T]TTAGTTACTGAAGTA	80013
rs189439005	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15808849	TAAATGGAGTACCAA[A/G]CAAATTAGCCACTGA	80013
rs189448310	snp	C/T	0.00279162	0.0372561	intron-variant	FAM188A	GRCh38.p7	10:15793981	TGACTGGCCTGTACA[C/T]GCCTATTTAATTAGG	80013
rs189493221	snp	C/T			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15780774	ATCCTATTTGTTTTC[C/T]AATCTTTTTGTTGGT	80013
rs189534724	snp	C/G	0.00318978	0.0398085	intron-variant	FAM188A	GRCh38.p7	10:15835931	TTATATTACAAACAC[C/G]AACTCCATCCATCAC	80013
rs189541365	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15835492	TCCTCCTAAACAATA[C/T]AAATCAGGCTATGAT	80013
rs189556717	snp	C/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15805281	AATAAACTTTAAAGA[C/G]CTTTTCAGTAATGAA	80013
rs189638254	snp	A/C/G	0.00914312	0.0669923	intron-variant	FAM188A	GRCh38.p7	10:15850083	TTTATAATTTCTTAC[A/C/G]CCTGTCTTTACTGCA	80013
rs189717872	snp	C/T	0.00358779	0.0422022	intron-variant	FAM188A	GRCh38.p7	10:15839826	AAATATGGTTTACTT[C/T]ATGGCAACTTTTAAA	80013
rs189722086	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15818622	GAACAGATAAAATTG[A/G]TTTAACATACAAAAG	80013
rs189732479	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15785664	GTCCAGTAGTCTACA[C/T]TGTCTACATTGTGAT	80013
rs189765402	snp	A/C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15822497	AACAACAAACAGGTA[A/C/T]GAAAAATCGATGCAT	80013
rs189765675	snp	C/T	0.00279162	0.0372561	intron-variant	FAM188A	GRCh38.p7	10:15845323	TCTATGATTGTATTA[C/T]GTATTTGGTTCCATT	80013
rs189769649	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15858428	AGGAAAAAGCCAAAG[A/G]GTGAATTTGGCATAG	80013
rs189769849	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15806975	AAGTAGTTAAATGCA[C/T]AGCTCAGAAGTCAGA	80013
rs189780174	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15791967	CAAATGTTGGATACT[C/G]AAAACTAACAGAGAA	80013
rs189786123	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15829287	TACCATTGTTTTTAA[C/T]GACCGGGAGGCAGAG	80013
rs189817597	snp	C/T	0.00358779	0.0422022	intron-variant	FAM188A	GRCh38.p7	10:15820898	GAGAATAACTTGAGG[C/T]CAAGAGTTTGAGACC	80013
rs189833404	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15789532	AAATACTTAAAAATA[C/T]TTTTTAACTTGAGAA	80013
rs189843407	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15781702	ACACTTCCTTCATAA[A/G]GTGCTGTGAAACTTA	80013
rs189963181	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15853032	CAAATACTGCAGAGC[A/G]TCTATGGATTTTGGT	80013
rs189967394	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15833277	GTATTTCACACCACC[A/T]GGCTTTGTAATGCTC	80013
rs189981562	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15801193	CATGGGGGGGAAATG[C/T]CATAAAGGACATTTA	80013
rs190050613	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15830352	CATTTTCTCACCTCA[C/T]TCTAACTATCCTGTG	80013
rs190059720	snp	A/G	0.00358779	0.0422022	intron-variant	FAM188A	GRCh38.p7	10:15854304	GCCTTTTCCAATTGC[A/G]TATGTGAGGCCAGAT	80013
rs190063982	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15824355	TTTTGATTTGTAGTT[C/T]TCTCATGATCAGTGA	80013
rs190145185	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15861242	GCTTTGAATTTAAAA[C/T]GAAAGGGCAAAATCT	80013
rs190208526	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15825349	TACTTTGTGATTATA[C/T]TCTTGTTTTCTTTGC	80013
rs190210688	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15810668	GTCAACAAAAAGTCA[G/T]TGAGCACCTACACTA	80013
rs190225000	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15795449	ATACAGCAACTTCCA[C/T]TTCTACACGGTACTT	80013
rs190229074	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	FAM188A	GRCh38.p7	10:15778428	ATCTGTGAATAAATG[G/T]TAATGGTCTCTTAGA	80013
rs190302401	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15841810	AAAGCCATCCAAATA[A/C]CACCACCAAGTAGAA	80013
rs190305351	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15841089	AATCCGTTTTTGCAA[C/T]ACCAAAGCAAAACAT	80013
rs190331054	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15809668	TTCTGTGGGAACCCT[A/G]CTGCTTGATGACTCT	80013
rs190382062	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15800743	CTCACTATGTCAAGA[C/T]AAATGAATCCAGCAT	80013
rs190498427	snp	C/G	0.00199481	0.0315187	intron-variant	FAM188A	GRCh38.p7	10:15844344	CAACATTTGAGAAGT[C/G]AGATGGGGATATTCA	80013
rs190518653	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15814567	TTCTACACCCACATG[G/T]CAGGAGTTTTTGTGT	80013
rs190536406	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15784188	ATAATAGTATGGTGT[C/T]TGGAAGGCACACAGT	80013
rs190579282	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15848356	TTACATGGCATTGGC[C/T]GGGCACAGTGGCTCA	80013
rs190700595	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15819250	CAAGCTCAATGACTT[C/T]CTTAATGCCATTCCT	80013
rs190706925	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15803792	ATTATCTTCCAAGAT[A/G]AAGTTCTAACAAATG	80013
rs190707576	snp	G/T	0.0107246	0.0724382	intron-variant	FAM188A	GRCh38.p7	10:15855361	AAGGTTTTACTTAAG[G/T]TTGAATTTCTCAGGA	80013
rs190710098	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15850959	ATAGAAAAGAACCTA[C/T]GTTGAAATATTGGGT	80013
rs190715800	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15842140	TTGAGCATTAGAATT[C/T]TATAGAAAATGGCGC	80013
rs190717299	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15786418	ACACATTCCCTCTGT[C/G]TGGGAAGGTTTCCAT	80013
rs190719614	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15826349	CAGCTTATTTCTGTT[C/G]TATTGGAGAAGCAAA	80013
rs190738751	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15857384	CTTCAAACTATTTAT[G/T]GTACATGTGTAATTT	80013
rs190763417	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15828397	GAGAAAGTAGATGAG[C/T]GGATGCTAGGGCTGG	80013
rs190784127	snp	A/C	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15798167	TGGTAATTTCTAAGT[A/C]TTATTTAAAACTATG	80013
rs190862656	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15798894	GTTCTGAACAGGCTA[A/T]ACAAGCTCACCTGCT	80013
rs190970835	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15837745	CGGCTTCTTTTAAAA[G/T]AAATTAATGTTACAT	80013
rs190999244	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15836932	GGTCAAGTGCTACAC[A/G]GAAGGATCAAAGGAA	80013
rs191000952	snp	A/G	0.00119737	0.0244387	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15785823	TTTTTCTATTTGTCA[A/G]TATGTCTCTCTAATA	80013
rs191021416	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15806417	GGAGGCTTGGATTAG[A/T]ATGAACAAAAAGTGA	80013
rs191107720	snp	A/C/T	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15815550	AATCAGGAAAGCACA[A/C/T]CACAATGAAGAAACC	80013
rs191126254	snp	G/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	FAM188A	GRCh38.p7	10:15782355	CATTTGACAAAAGAA[G/T]GAACTTAGGTTTATG	80013
rs191145257	snp	A/T	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15836292	CCTCATGCATCAAGG[A/T]CCTATCTCTGTCAGA	80013
rs191147578	snp	A/G	0.00676609	0.0577691	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15782675	AATTTGGCCCACGAT[A/G]TTTAATTAGTGGTTT	80013
rs191151561	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15821940	TGGGTAAATGTGATG[C/G]TTTAGATGTATATTA	80013
rs191155291	snp	A/G	0.00318978	0.0398085	intron-variant	FAM188A	GRCh38.p7	10:15805924	TATGGTGGCTGTGGT[A/G]TGCTCCAGTACAGCC	80013
rs191161930	snp	G/T	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15790814	TTGGCACTCAAAATT[G/T]TGGAGGATCAACCTT	80013
rs191249619	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15850514	CTCTAAAATGGCCGC[C/T]CGGGGAGTGTCTTAT	80013
rs191261268	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15822178	CACTTGCCTAATACT[G/T]AAAACATGGACATTT	80013
rs191291230	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15788149	CTTGAGTTAATTCTC[G/T]TTTGTAAATTAGAGC	80013
rs191331413	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15861814	TTTTTCCTATTTATA[C/T]GTTATTTCTAATTTT	80013
rs191341298	snp	A/C	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15839827	AATATGGTTTACTTC[A/C]TGGCAACTTTTAAAA	80013
rs191343476	snp	A/G	0.00318978	0.0398085	intron-variant	FAM188A	GRCh38.p7	10:15846215	AACACCCACTTGCAA[A/G]AATAACTACCACTAC	80013
rs191345411	snp	A/C	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15823360	AATTACCTTTTTACA[A/C]TTACTCTCTCATAAG	80013
rs191347592	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15808663	AATTCAGTTTCTTTA[G/T]ATGAACAGTTCTGTC	80013
rs191356467	snp	C/T	0.0399052	0.1355	intron-variant	FAM188A	GRCh38.p7	10:15848450	CCATCCTGGCTAACA[C/T]GATGAAACCCCGTCT	80013
rs191365721	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15819680	CCTGCATGTGGCCCT[A/G]CCTGGCTTCCCTCCC	80013
rs191374266	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15791281	AAAAAATTCCTTAGA[A/G]AAAGGCCAGAATCAT	80013
rs191599506	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15854941	TTTGGCCAGCTCTTC[C/T]ACTGAGAATAAGGAA	80013
rs191607553	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15834020	CTTTAAAAATGAATA[C/T]ATAATTATTAATATT	80013
rs191625109	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15804180	TGCAAAACAATATAG[C/T]TTTTAAAATTATCTA	80013
rs191626145	snp	A/G	0.00478085	0.0486577	intron-variant	FAM188A	GRCh38.p7	10:15816719	TGAGATTTTTGAACA[A/G]TTCATTTGTTGTGGG	80013
rs191638273	snp	G/T	0.00438332	0.0466095	intron-variant	FAM188A	GRCh38.p7	10:15799381	TTTTTGTATTTTTAG[G/T]AGAGACCGGGTTTCA	80013
rs191643083	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15783108	CTGCTGGCAACTGGA[A/G]CTTCAGCTCCTACAG	80013
rs191689532	snp	A/T	0.0310518	0.120672	intron-variant	FAM188A	GRCh38.p7	10:15795047	CTAGTAAAACAAAAC[A/T]CAACACAACACATAA	80013
rs191815058	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15811509	GTGATATTCACTTCT[A/G]ACACAACACAAACAC	80013
rs191816820	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15833378	AAATCCCAGTTTTAT[A/G]CCACAGAAAATGAAA	80013
rs191817865	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15856349	TAACAAAAATTGTGC[C/T]ACACTGAAAGCCCAA	80013
rs191832646	snp	A/C	0.000798403	0.0199641	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	FAM188A	GRCh38.p7	10:15778672	ATAGTAACTGTGATA[A/C]TTAATATACAAATGC	80013
rs191882571	snp	A/C	0.000399281	0.0141238	downstream-variant-500B	FAM188A	GRCh38.p7	10:15778008	GCTTCTGGCTGGCTG[A/C]GTTAGCAGAGCTCTT	80013
rs191907426	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15827532	TGGGTGACAGAGTGA[A/G]ACTCCGTCTCAATAA	80013
rs191909815	snp	C/T	0.00676609	0.0577691	intron-variant	FAM188A	GRCh38.p7	10:15843150	GACTTTCTCAGATAA[C/T]TTTAGATCATCTCTA	80013
rs191924228	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15803396	AAGTTTGAAGAGCAA[A/G]TATAGAATTACATTC	80013
rs191927160	snp	A/T	0.00795532	0.062565	intron-variant	FAM188A	GRCh38.p7	10:15813428	TAGGCATCAATTTTT[A/T]AAGTAAACATCCCAA	80013
rs191929050	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15797368	ATGCACAGTTGTCTC[C/T]CATTTACCATCCCTT	80013
rs191941619	snp	C/T	0.00159617	0.0282053	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15779781	AAAGTAAAAGAGACG[C/T]TGAAAGATCAAACTA	80013
rs191987421	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15849180	CAGGCTCATCTTGAA[C/T]AGGAATTTGCCAGAG	80013
rs192013511	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15835076	TAATTATTTAACTGG[A/T]ACATAAAATGGAAGG	80013
rs192019776	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15820684	GATTATCATATGCAT[A/G]TCACCCAGTGTTCAA	80013
rs192022277	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15805001	CAGACAGCCCTCTGA[C/T]GTTCTTCCTCTAGAA	80013
rs192119237	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15848169	ACACAATTTTGCACC[A/C]AGGAACTCCTCTAGG	80013
rs192121796	snp	A/C	0.0399052	0.1355	intron-variant	FAM188A	GRCh38.p7	10:15845778	TCCCAAAGTGCTGGG[A/C]TTACAGGTGTGAGCC	80013
rs192125387	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15796334	ATAAACTCTCCAGGC[C/T]ATTTATTTTACGTCT	80013
rs192131907	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15815986	AATATTCAGATATGG[C/T]GGGGCACAGTGGCTC	80013
rs192133553	snp	G/T	0.00636936	0.0560724	intron-variant	FAM188A	GRCh38.p7	10:15818875	TTAGAGCTCCTTTTG[G/T]GGGTAAGGAAAACAT	80013
rs192254189	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15831306	ATCAGCCTGGCAGTG[A/G]GAGGGAAAATGTGTA	80013
rs192261940	snp	A/C	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15800035	CAACATGGATATGAA[A/C]TGCATGGGTCCACTT	80013
rs192298730	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15820374	TCTTAAGGGATACAC[A/G]GGAAATATTTCCAAA	80013
rs192304530	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15853155	GAAGGGTAGTTGGAT[C/G]AAGAATTATTAATTT	80013
rs192314081	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15804657	AATAAAAGGTAAATG[C/T]TGTATAATTTACCTT	80013
rs192321531	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15788773	ATGCCATAATATATT[A/G]CAGCCATCCCTAAAA	80013
rs192408530	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15844140	TTTGCAGCGAAGATT[A/G]TATGAGAAAATCTAT	80013
rs192412674	snp	A/T	0.00517822	0.0506191	intron-variant	FAM188A	GRCh38.p7	10:15857187	CTAACTTCCTTCTTG[A/T]TCCTTAAACAGACCA	80013
rs192413038	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15799179	ATAATATATTACATA[C/T]TTTTTCCCCCAAATG	80013
rs192469987	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15858821	TTTTTTCTTAGTCTT[A/T]CACAGTATTTTAGAG	80013
rs192510185	snp	C/G	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15830026	TCGAGAATGGAGAAT[C/G]TCGAAGACTCAGCAA	80013
rs192529182	snp	C/G	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15807829	GGAAATCACAAAAAC[C/G]AGAATATACAAATAC	80013
rs192599260	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15839498	CTACCTAATCTTTTC[C/G]AAATTATACTGCTTG	80013
rs192653251	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15852019	CCGCTACTCTCCATA[C/T]AGATAAATCCTTATT	80013
rs192665993	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15800830	CCTTCCGCTTTTTGC[A/C]AAATACCTCCTTGTA	80013
rs192671951	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15823128	CTACAACATCTAGAT[A/G]GTGTAAGGCAAGAGC	80013
rs192672068	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15838411	TAAAATTCTCAGTTT[A/G]TTTTCAACTTCATTA	80013
rs192680058	snp	A/C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15784629	GTAGTCCCAGCTACA[A/C/T]AGGAGGCTGAGGCAG	80013
rs192689428	snp	A/G	0.0023933	0.0345097	intron-variant	FAM188A	GRCh38.p7	10:15807362	GAATCAGCGGACACA[A/G]TACGAATGGTGGAAG	80013
rs192742873	snp	C/T	0.00199481	0.0315187	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15783740	ACTCAAAATGCCTTA[C/T]AGAAAATAGAAAAAT	80013
rs192819637	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15792825	TGAAAACCTGTGATT[A/G]GCAGTTCAGACACTA	80013
rs192855635	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15852860	GGAAAAAAACGATGG[C/T]TGGGTCTGTACTAAA	80013
rs192862275	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15855990	TATGCTTACCAATTA[C/T]GAATTAAGAAATATT	80013
rs192863109	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15823253	GATCAGGTAGAGCAA[C/T]GGTTCTTCAATTGTG	80013
rs192873580	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15827222	AGAAGCCATCTAAAA[A/C]AAAGACCAAATGATT	80013
rs192933952	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15796906	TGACACACATGAATC[C/T]AAAATGTAGGCTCCT	80013
rs193005305	snp	G/T	0.00358779	0.0422022	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15780871	GACCAAGGACAGGAT[G/T]GGGAATCAGGAACTC	80013
rs193046680	snp	A/T	0.00318978	0.0398085	intron-variant	FAM188A	GRCh38.p7	10:15814046	TTGCTCAAATGCAGA[A/T]ATGTTAAAGAAGGAA	80013
rs193047084	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15834802	GTTCCTCAAATATCT[C/T]TTATTTTCTTTCATG	80013
rs193073348	snp	A/C	0.00716266	0.059414	intron-variant	FAM188A	GRCh38.p7	10:15842422	TAAGAAATAGTATAA[A/C]TTTTATTAAAAGTTC	80013
rs193080360	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15789409	CCAGGAAAAAAAAAT[C/T]GCATAAAAAATACAA	80013
rs193111161	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15846978	TCCACCCACCTTGGC[A/C]TCCCAAAGTGGTAGG	80013
rs193140698	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15817367	ACATCTTTGCTCCCA[A/G]ATAATCAAGAAAAAT	80013
rs193150982	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15792260	ACTTCTGGCTCCCCA[A/G]TGGGCAATGAGTTCT	80013
rs193168336	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15812305	TAGTATAATTATCCC[C/T]TCTCAATTATTCATG	80013
rs193171204	snp	C/T	1.65913e-05	0.00288017	missense, downstream-variant-500B, nc-transcript-variant	FAM188A	GRCh38.p7	10:15779086	GGAGTGTCATCTGTC[C/T]GTAGCATGGGATCTT	80013
rs193225614	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15828261	AGGAGTGAAGTACTG[A/G]TACATGCTAAAACAT	80013
rs193227907	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15848762	ACTGATAGCAGCTAG[C/T]GGAAGTTCTTCAGAT	80013
rs193227968	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15797848	ATCACTCCCAAACCT[G/T]AGTTGCAGATTTCTA	80013
rs193260180	snp	A/T	0.00119737	0.0244387	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15862087	ATGTGTAACTTGCTT[A/T]TGACAATTCCTATCA	80013
rs193264208	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15832095	GCAGAAGAGTATTCT[C/G]GTTTGGGGACTAGGG	80013
rs199510240	in-del	-/TTATAT	0.0192547	0.0962112	intron-variant, downstream-variant-500B	FAM188A	GRCh38.p7	10:15782260	TATTAACACTTTAAA[-/TTATAT]TTATATCAGGCAATT	80013
rs199529548	in-del	-/A	0.0189856	0.0955633	intron-variant	FAM188A	GRCh38.p7	10:15848856	ACCTGCTTGGGCCTC[-/A]GTGTTCTCATTAAAA	80013
rs199562837	snp	C/T	8.30599e-05	0.00644384	missense, downstream-variant-500B, nc-transcript-variant	FAM188A	GRCh38.p7	10:15779132	CTGCAGTCCCTTCTA[C/T]GTACATGACCTGTTG	80013
rs199567480	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15825492	TGAGATTAAAAGGCA[G/T]AAGCCAATACACCCA	80013
rs199613061	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15829133	TAATAGAATGAAGCC[G/T]ACTGAGGTAAAGCAC	80013
rs199620164	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15798482	TTTTTTTTTTTTTTA[A/T]ATACTCTGCTAGTGG	80013
rs199633488	in-del	-/A			intron-variant	FAM188A	GRCh38.p7	10:15813994	AAAAAAAAAAAAAAA[-/A]GAAAAAGAAAAAAGA	80013
rs199663495	snp	C/T	0.000231596	0.0107585	missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15837260	ATTTATTTCCCCACA[C/T]TGAATACTGGTCCAA	80013
rs199736107	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15862182	TGCCTATTCATAATT[C/T]TAGCATGGGGCCTTG	80013
rs199785123	in-del	-/G	0.0236746	0.106192	intron-variant	FAM188A	GRCh38.p7	10:15793851	GCAAATGCCACACAT[-/G]CATTCTTAGATAGAT	80013
rs199792130	snp	A/T	0.29175	0.246489	intron-variant	FAM188A	GRCh38.p7	10:15816281	AAAAAAAAAAAAAAA[A/T]GAAAAAGAAAAAAAA	80013
rs199833154	snp	C/G/T	0.000567553	0.016837	intron-variant	FAM188A	GRCh38.p7	10:15834637	GAAACAGAATTCATT[C/G/T]ACTTATTTTAAAAAA	80013
rs199868057	snp	C/T	4.95724e-05	0.00497833	utr-variant-5-prime, missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15841548	TGGTCACAACAAGCA[C/T]TTTCTAAAATATCAC	80013
rs200060239	snp	C/T	6.65148e-05	0.00576654	intron-variant	FAM188A	GRCh38.p7	10:15786652	ATGAGATTTATACTA[C/T]GGGGAGAAAGAAGAA	80013
rs200183180	in-del	-/AG			intron-variant	FAM188A	GRCh38.p7	10:15816287	AAAAAAAAATGAAAA[-/AG]AAAAAAAATAAAAAA	80013
rs200279432	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15794934	GCCTTTATTCTTTAA[C/T]AGTTATTATCTCCTA	80013
rs200295148	in-del	-/ATGGTAAAAT			intron-variant	FAM188A	GRCh38.p7	10:15827358	ACCAGCCTGGCTAAC[-/ATGGTAAAAT]CCCGTCTCTACTAAA	80013
rs200308221	snp	G/T	0.031825	0.122064	intron-variant	FAM188A	GRCh38.p7	10:15813779	GCCAAATTACAGACT[G/T]CCTTAAAAATTATGC	80013
rs200326350	snp	C/T	0.000858411	0.0206995	intron-variant	FAM188A	GRCh38.p7	10:15847842	TGTCCCTCTAAGGAG[C/T]TGGTAAAGGAGTCTA	80013
rs200364714	in-del	-/CT	0.00676609	0.0577691	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15786412	TCGAACACACATTCC[-/CT]CTGTCTGGGAAGGTT	80013
rs200385721	snp	A/C	0.00199809	0.0315445	intron-variant	FAM188A	GRCh38.p7	10:15821734	AAGAAGTTCTGCAAA[A/C]AACAACAACAACAAC	80013
rs200390594	snp	A/G	0.000204778	0.0101167	intron-variant	FAM188A	GRCh38.p7	10:15847992	TATAATTCAAGTAGC[A/G]GCTAAAAGAATCTTT	80013
rs200421665	snp	A/G	0.000132875	0.00814983	missense, intron-variant, nc-transcript-variant	FAM188A	GRCh38.p7	10:15786646	TTCTTCATGAGATTT[A/G]TACTACGGGGAGAAA	80013
rs200488243	snp	A/G	1.69905e-05	0.00291461	intron-variant	FAM188A	GRCh38.p7	10:15838217	ATTTTAAATGTTCCA[A/G]TGTTACTTACTGAAT	80013
rs200504478	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15846212	CATAACACCCACTTG[A/C]AAAAATAACTACCAC	80013
rs200661001	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15834627	ATGCCCTAAAGAAAC[A/G]GAATTCATTGACTTA	80013
rs200791705	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15803638	ACATAAAACCATAAT[C/T]TCTTAAACATTTGGC	80013
rs200800081	in-del	-/CC			intron-variant	FAM188A	GRCh38.p7	10:15795002	AGAAAGTCATTCACT[-/CC]CCGTTTCAACTGTGG	80013
rs200808072	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15849461	GTTTTTTTTTTTTTT[A/G]TTTTTCCTTTTTTAA	80013
rs200843384	in-del	-/AAC	0.0179999	0.0931448	intron-variant	FAM188A	GRCh38.p7	10:15821735	AGAAGTTCTGCAAAA[-/AAC]AACAACAACAACAAA	80013
rs200855010	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15817769	AATTCCAAGTGGCTG[G/T]TTGTGGCAGTCAGGC	80013
rs200926509	snp	A/T	1.65102e-05	0.00287312	intron-variant	FAM188A	GRCh38.p7	10:15843208	TAAAAGACAGCTATC[A/T]TACCTGAACAATCCC	80013
rs200937570	in-del	-/G			intron-variant	FAM188A	GRCh38.p7	10:15849444	TAATATCATCTTACT[-/G]GGTTTTTTTTTTTTT	80013
rs200981269	snp	A/C/G	6.65064e-05	0.00576623	missense, downstream-variant-500B, nc-transcript-variant	FAM188A	GRCh38.p7	10:15779137	GTCCCTTCTACGTAC[A/C/G]TGACCTGTTGAACAA	80013
rs201003144	snp	G/T	1.6522e-05	0.00287414	utr-variant-5-prime, missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15841530	AAGCAGTATGATCCA[G/T]AGTGGTCACAACAAG	80013
rs201014978	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15794007	TTAGGAATATACCCA[C/T]AGCACAGTGTTAACA	80013
rs201025578	in-del	-/TAAA			intron-variant	FAM188A	GRCh38.p7	10:15808186	GTTATTTTAAGGTCT[-/TAAA]AGTCACAGAAGTTAT	80013
rs201042238	in-del	-/A	0.0150606	0.0854603	intron-variant	FAM188A	GRCh38.p7	10:15857713	CACCCCGCATTTTTT[-/A]AAACGAACAGGGATT	80013
rs201062340	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15810723	GCAAACAGTAGGTGA[A/C]AAAACACAAAAATCC	80013
rs201064606	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15824300	TTTTGTTGTTTTTTA[A/C]CAGCCATTCTGACTG	80013
rs201066315	snp	C/T	0.000153988	0.00877328	utr-variant-5-prime, missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15860284	GCTCCATCAGCTCTT[C/T]AGTCAGTTCGGACAT	80013
rs201123093	snp	A/G	0.00187634	0.0305721	intron-variant	FAM188A	GRCh38.p7	10:15847958	CCTAAAAATGAAAGC[A/G]AGTAGGAAAGATTAA	80013
rs201290875	snp	C/T	0.00199481	0.0315187	intron-variant	FAM188A	GRCh38.p7	10:15815800	TATTATGAATCCCTA[C/T]TTTAAAGACACAGGA	80013
rs201309720	snp	C/T	0.031825	0.122064	intron-variant	FAM188A	GRCh38.p7	10:15813780	CCAAATTACAGACTG[C/T]CTTAAAAATTATGCA	80013
rs201340917	snp	C/G	1.68383e-05	0.00290153	intron-variant	FAM188A	GRCh38.p7	10:15834626	AATGCCCTAAAGAAA[C/G]AGAATTCATTGACTT	80013
rs201352822	snp	A/G	0.000798403	0.0199641	missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15833683	GAAACAGCATGTCCC[A/G]TCAGCAGGAGATTAA	80013
rs201377440	snp	C/G	0.000727909	0.0190637	intron-variant	FAM188A	GRCh38.p7	10:15833753	ATATGAATATAGTTG[C/G]CAAATCAAATAATTC	80013
rs201380851	snp	C/T	0.000117516	0.00766447	intron-variant	FAM188A	GRCh38.p7	10:15816798	TACTTGTTTGCCTGA[C/T]GTCATAACTTAAAAA	80013
rs201539365	in-del	-/A	0.040671	0.13668	intron-variant	FAM188A	GRCh38.p7	10:15834273	TAAATTTTCTCATTT[-/A]AAAAAAATTACAAAT	80013
rs201568467	in-del	-/T			intron-variant	FAM188A	GRCh38.p7	10:15849447	ATATCATCTTACTGG[-/T]TTTTTTTTTTTTTCT	80013
rs201589742	snp	A/C	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15821910	TTATAAAATACCATT[A/C]GATCAGGTTTGTGGT	80013
rs201610339	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15798481	TTTTTTTTTTTTTTT[A/T]AATACTCTGCTAGTG	80013
rs201669272	snp	A/C	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15802307	GTGGGGTAATTTATA[A/C]ATAAAAGGTTTAACT	80013
rs201669904	snp	A/T	0.00013219	0.00812881	missense, intron-variant, nc-transcript-variant	FAM188A	GRCh38.p7	10:15816887	ACAATCCAAATAGGG[A/T]ATTTTGGAGATTTCA	80013
rs201860178	in-del	-/A	0.0387552	0.1337	intron-variant	FAM188A	GRCh38.p7	10:15813878	ACATATCAGTTTTAT[-/A]AAAAAAAGACATAAA	80013
rs201904501	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15832689	GAACTTAGTTCTTAA[A/T]TTTTTTAAACAGTAA	80013
rs201974094	snp	A/T	0.00299544	0.0385843	intron-variant	FAM188A	GRCh38.p7	10:15816809	CTGATGTCATAACTT[A/T]AAAAAAAATCCTGCT	80013
rs202042665	snp	A/C	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15794634	ATGCATCTCTCACAA[A/C]TCAATTCTGAAAAAT	80013
rs202109754	in-del	-/TG	0.0142736	0.0832652	intron-variant	FAM188A	GRCh38.p7	10:15828499	ATGGCTAAACAACTC[-/TG]AGAAAATATTTAAAA	80013
rs202124675	in-del	-/A			intron-variant	FAM188A	GRCh38.p7	10:15836858	ACACAGTGATTTTTC[-/A]AAAAAAAAAATCAAG	80013
rs202125885	snp	C/T	0.031825	0.122064	intron-variant	FAM188A	GRCh38.p7	10:15813778	CGCCAAATTACAGAC[C/T]GCCTTAAAAATTATG	80013
rs202127209	snp	A/G	1.65378e-05	0.00287552	synonymous-codon, nc-transcript-variant	FAM188A	GRCh38.p7	10:15833691	ATGTCCCGTCAGCAG[A/G]AGATTAATTAAACTT	80013
rs367679592	in-del	-/T	0.331411	0.236373	intron-variant	FAM188A	GRCh38.p7	10:15853736	AGCTGAACCAGCTAC[-/T]TTTTTTTTTTTAATG	80013
rs367683208	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15807740	AAAATTCAGTGGAAA[A/G]GAGAGACTTCTTCCA	80013
rs367723586	in-del	-/GAG			intron-variant	FAM188A	GRCh38.p7	10:15829168	GATGATCAGAGGGAG[-/GAG]AAAACTTTTCCTGCT	80013
rs367727729	in-del	-/ACACAACACA/T			intron-variant	FAM188A	GRCh38.p7	10:15795059	ACACAACACAACACA[-/ACACAACACA/T]TAACGATTACATGAA	80013
rs367821028	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15798084	TTCGCCATCTGTTAC[A/G]TTCTCAACCTTTTTT	80013
rs367858904	snp	A/T	0.00279162	0.0372561	intron-variant	FAM188A	GRCh38.p7	10:15823882	TTTAGATCCCACATA[A/T]AAGTAAGAGCGTGTG	80013
rs367872580	in-del	-/TATTTATTAGGAGATAATGTCAAC	0.0944967	0.195752	intron-variant	FAM188A	GRCh38.p7	10:15821873	TTAAAACTTAGCATG[-/TATTTATTAGGAGATAATGTCAAC]TAATCATTACAGTAC	80013
rs367890407	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15801138	GAAAGAATATCTGCC[G/T]GAACAGGTTTTTAAT	80013
rs367933326	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15819052	CACCTTATTCTTTGT[C/T]GGGTTTGTACGTGTG	80013
rs367950688	snp	C/T	0.00199481	0.0315187	intron-variant	FAM188A	GRCh38.p7	10:15829673	AAAATCATTAACTTG[C/T]CAGTTTGCAGAATAT	80013
rs367986162	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15792194	AAGTGACCTTTTCCC[A/C]AAGGCCAAGTCACAC	80013
rs367992302	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15846784	GCTGGAGTACAGTGG[C/T]GCAATCTCGGCTCAC	80013
rs368010120	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15781148	TGCAAAGAATATACA[C/T]TGTCAAGAAAATTTG	80013
rs368051734	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15799897	CTTCTCGTGAGCTAT[G/T]AGAAATAGAATATTA	80013
rs368071018	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15837186	TCAAAGGCAGAAAAA[C/T]CATCTTCTTGAACAC	80013
rs368073968	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15809904	AGAAAATATGATTTA[C/T]AAAACATGGTGGTTT	80013
rs368139484	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15796345	AGGCCATTTATTTTA[C/T]GTCTGAAAAGTGGCA	80013
rs368207347	snp	A/G	0.000153988	0.00877328	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15779185	CAAGCAACAGTCTTA[A/G]CAAATTCTTATGTGG	80013
rs368497014	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15790775	TGATCTGGTCCAAAA[C/T]CTGAAATGCTCCACG	80013
rs368560629	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15787859	TGTGTTTAATTCATT[C/T]AATCCTTAGGATGGC	80013
rs368594137	snp	A/G/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15810610	CATGGTCATCTCACA[A/G/T]TTTTTTTAAGATGGA	80013
rs368626888	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15837918	AATATTTATCCTACT[A/G]GAAATCTTCATATTT	80013
rs368692604	snp	A/G	0.000153988	0.00877328	missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15789266	CAGGATCTGAAACAA[A/G]GTCCAATGCTTTCAT	80013
rs368716588	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15858131	AAACCAGTAACAGGA[A/C]CCCTCTGATTCAGAG	80013
rs368757671	in-del	-/CAATGAA			intron-variant	FAM188A	GRCh38.p7	10:15818697	AAAAACAGAGATGAA[-/CAATGAA]AACACCATGCTAAGT	80013
rs368767614	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15829397	GCTGACAACAATTCC[A/G]TTACAATCTCTAGGT	80013
rs368768162	snp	A/G			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15782642	CTAAATACACTTCCA[A/G]TATGTACCAATACTT	80013
rs368771246	in-del	-/AACA			intron-variant	FAM188A	GRCh38.p7	10:15792705	CAACTTAACAAAACA[-/AACA]GCTTCAGATTTAAAA	80013
rs368840500	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15791092	TATTCTGAAGTGTAA[C/T]CATAACTGTACCCGG	80013
rs368851197	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15826818	ACTGGAATTAGGACA[C/T]TAGATAATTCTTTGA	80013
rs368881349	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15827577	AAATAAATAAATAAA[A/T]GCCTTGGATATAAAA	80013
rs368901957	snp	C/T	3.29897e-05	0.00406125	intron-variant	FAM188A	GRCh38.p7	10:15847858	TGGTAAAGGAGTCTA[C/T]GTTACCTGAACAGGT	80013
rs368912846	in-del	-/AAT			intron-variant, cds-indel	FAM188A	GRCh38.p7	10:15857929	TGCTTCCAGAAAACT[-/AAT]GAGACTGCAGTTGTC	80013
rs368920107	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15846102	TGCTGGGATTACAGG[C/T]ATGAGCCACCACGCC	80013
rs368970720	in-del	-/CA			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15786449	GTAACGGTGTTTTCT[-/CA]GTCTCATATCTGCGC	80013
rs369047036	in-del	-/TA			intron-variant	FAM188A	GRCh38.p7	10:15789770	CAGTGATCCACTGAT[-/TA]ACTTAGACAACTGAC	80013
rs369167253	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15805513	AATCACCTAGTGATA[C/G]AAGGTAATCGATGGT	80013
rs369215319	snp	G/T			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15785665	TCCAGTAGTCTACAT[G/T]GTCTACATTGTGATA	80013
rs369216588	in-del	-/A			intron-variant	FAM188A	GRCh38.p7	10:15826090	CAAAATCAAAGAAAA[-/A]CTTTAGCTCAACATA	80013
rs369224339	snp	A/C	0.000276679	0.0117585	intron-variant	FAM188A	GRCh38.p7	10:15860174	GGGCAAAAGAAGCAG[A/C]GGCTGCAAGTGTGAG	80013
rs369282677	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15801740	AAGAGGCCATCACTG[A/T]TACAGAAAAAGCTAA	80013
rs369292676	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15794647	AACTCAATTCTGAAA[A/G]ATTGCACTGATTATA	80013
rs369315748	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15816297	GAAAAAGAAAAAAAA[A/T]AAAAAAGACAAGAAA	80013
rs369315783	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15804004	AAGAGATCCTACACA[G/T]GAGACTCAACGATTA	80013
rs369323055	snp	A/G	1.6501e-05	0.00287232	utr-variant-5-prime, missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15843241	CAAGAAGACTTCTCC[A/G]AAGAAAACAGGAGCT	80013
rs369326444	snp	C/T	0.00716266	0.059414	intron-variant	FAM188A	GRCh38.p7	10:15827463	GGAGAATTGCTTGAA[C/T]CCGGGTTAGGCAGAG	80013
rs369337342	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15852738	GGTTGAAGTGTAATT[A/C]GGATTAGAAAGAGAA	80013
rs369338994	snp	A/G			utr-variant-5-prime, nc-transcript-variant	FAM188A	GRCh38.p7	10:15860480	TCAAGCCAGGTTGGG[A/G]CAGCAGCGAGTTTTC	80013
rs369339034	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15812844	TCTAAGATCTAATCA[C/T]TAGCCACACCTATCT	80013
rs369341508	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15826992	GGGCATGATGGTGCA[C/T]GTCTGTAGTCTCAGC	80013
rs369350483	snp	A/G/T	3.62353e-05	0.00425636	intron-variant, downstream-variant-500B	FAM188A	GRCh38.p7	10:15782122	TATTTCATCAACCCA[A/G/T]TTGAACACCGACGAC	80013
rs369442931	snp	C/T	1.67441e-05	0.0028934	intron-variant	FAM188A	GRCh38.p7	10:15821638	AAAACATTCAAAGTA[C/T]CTTAAAAATCAATTT	80013
rs369444882	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15820430	ATACAAGACGCAGGC[A/G]TGCGTGCACATCCCA	80013
rs369451725	snp	A/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15847451	AATTTGAAAAAGTTA[A/T]AAGCCAGAAAAATAT	80013
rs369452204	snp	C/G			missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15833631	AGGAATATACTTACT[C/G]ATTCCTGAGCACTCT	80013
rs369501499	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15842457	CAAAAATAGTATCTC[A/G]AATAGTTTCTTCTCT	80013
rs369505038	snp	A/G			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15786352	TAGACTGGTGTCTGC[A/G]TCATCTTCTGCTGCC	80013
rs369509602	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15830320	GCTCAAGGACTTGAT[A/G]AATATCTCTTTTTTG	80013
rs369522793	snp	C/G			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15785251	CAACAAGTAAACAGT[C/G]AGAGAGGAACACAGA	80013
rs369522904	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15805171	CTAACTTTAACAAAT[C/T]CGTCAAGCTTTTCTT	80013
rs369570103	snp	A/G			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15782952	GGCCATTACAGGCCT[A/G]GCTCCCAGTGATTTC	80013
rs369615782	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15807067	TCTCACTGGCCCCAG[A/G]CTGTAACATGCAGAT	80013
rs369630119	snp	C/T			upstream-variant-2KB	FAM188A	GRCh38.p7	10:15860628	CGGTGGAAGTAGCTT[C/T]TGACCTTTCTGAACT	80013
rs369705646	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15844898	GCTTCCTAGTGAGGG[G/T]GAGCATCCTGATTAT	80013
rs369718768	snp	A/G			upstream-variant-2KB	FAM188A	GRCh38.p7	10:15861462	AAAGGGAGATTGCAT[A/G]CATTTCATATATTGT	80013
rs369813673	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15818330	AGTAAAAAAAAAAAA[A/C]AAACAAACAAAGGAT	80013
rs369821482	snp	A/C	0.00119737	0.0244387	intron-variant, downstream-variant-500B	FAM188A	GRCh38.p7	10:15782301	TCAACTGAAAGTAAA[A/C]TGCATGTTTCTCAAA	80013
rs369826130	snp	A/C	1.65485e-05	0.00287645	intron-variant	FAM188A	GRCh38.p7	10:15843307	TAATTAGTGAAATGC[A/C]TTATAACCATACATC	80013
rs369833688	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15797369	TGCACAGTTGTCTCT[C/T]ATTTACCATCCCTTG	80013
rs369901147	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15813881	ATATCAGTTTTATAA[A/T]AAAAGACATAAATAT	80013
rs369943116	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15798464	CTCTAAGTGCCAAGT[G/T]TTTTTTTTTTTTTTT	80013
rs369951362	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15819942	TACATCTAGAAAACC[A/C]AACAATTCTGGTGAA	80013
rs370002522	snp	A/T	1.65356e-05	0.00287533	missense, intron-variant, nc-transcript-variant	FAM188A	GRCh38.p7	10:15816903	ATTTTGGAGATTTCA[A/T]GTAAGAACCAACCTA	80013
rs370042210	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15848266	GTCTACTAAATTCAA[A/G]CAATTTTTAGAACTC	80013
rs370049806	snp	A/C/G			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15779254	ACATAGTTTCAGATG[A/C/G]AACTTGACATGTAAT	80013
rs370057014	snp	C/T	0.000153988	0.00877328	missense, downstream-variant-500B, nc-transcript-variant	FAM188A	GRCh38.p7	10:15782165	CATACCTTTTCATTA[C/T]AATTTGACTGCTTCA	80013
rs370086321	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15819788	AAGCCTTAAATCTCA[A/T]TTAAAACCATAGTTA	80013
rs370097284	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15852214	CTGTGTTACTGGTCA[C/T]TGTTTTCCCACAGTA	80013
rs370107173	snp	A/C	1.66125e-05	0.00288201	intron-variant	FAM188A	GRCh38.p7	10:15834523	TTCACATGAGGAGAC[A/C]AGAGATTTTAGTTAA	80013
rs370138746	snp	A/G	0.00279162	0.0372561	intron-variant	FAM188A	GRCh38.p7	10:15847631	TGAAAGTCAGGGAAC[A/G]CCTATTATTTTTCCT	80013
rs370193263	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15829598	TTTAGTTGGCAAGCA[C/T]TAGCAAGAGAGTCAT	80013
rs370206114	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15809480	GATACGATTTCTGAA[A/G]ACCCATGCCTACAGG	80013
rs370219574	in-del	-/ATCT			intron-variant	FAM188A	GRCh38.p7	10:15793768	GATCCCTGCCTATCT[-/ATCT]CCTAGGTTTGTGGCA	80013
rs370238576	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15850339	TGGCTGCAGTGTTCA[C/G]GGAACAAGGGAGATG	80013
rs370282263	snp	A/G	0.000153988	0.00877328	missense, downstream-variant-500B, nc-transcript-variant	FAM188A	GRCh38.p7	10:15779017	GAAGGAGAGCGATCT[A/G]TGGTCCAGAGTAACT	80013
rs370329867	snp	A/C			upstream-variant-2KB	FAM188A	GRCh38.p7	10:15862270	AATAAAGAATTCATT[A/C]TCTCTCAGCAAGTGA	80013
rs370351507	in-del	-/TTGGAGATC			intron-variant, cds-indel	FAM188A	GRCh38.p7	10:15785098	ATTTCTAACAAGCTC[-/TTGGAGATC]ATACTGAGAACTCAC	80013
rs370379555	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15790282	TTAAACCTCTTTTCT[A/G]TTCTTAAACCTCATA	80013
rs370418599	snp	A/G	1.69781e-05	0.00291355	intron-variant	FAM188A	GRCh38.p7	10:15789236	TAAATAACACTTCCT[A/G]TTTAGCTTACTATTC	80013
rs370464190	in-del	-/A			intron-variant	FAM188A	GRCh38.p7	10:15842904	GCTAAATAAGACTAC[-/A]AAAAAAAAAAAAAAA	80013
rs370623250	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15836700	CCATAAAAGGCATAC[C/T]GGATCCAGGGAAGAA	80013
rs370637730	snp	C/T	0.000433617	0.014718	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	FAM188A	GRCh38.p7	10:15778959	TCTTTCAACATCTGT[C/T]ATTAAGATCTTCCTT	80013
rs370653091	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15821536	GGGATAGGAAGGAAG[A/G]AGAGAGCGGTACTGA	80013
rs370670311	snp	C/T	5.01291e-05	0.0050062	missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15789302	CTTCCAGAAGTGAAT[C/T]GGGTATGAATCCATT	80013
rs370691272	snp	C/T	0.000153988	0.00877328	intron-variant	FAM188A	GRCh38.p7	10:15847846	CCTCTAAGGAGTTGG[C/T]AAAGGAGTCTATGTT	80013
rs370707757	in-del	-/GAA			intron-variant	FAM188A	GRCh38.p7	10:15841318	GCTTAAGCTGGAAAA[-/GAA]TACATGTTATGAAAA	80013
rs370728440	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15845614	AAAGACCCTCCCCTT[C/T]TAGCCTCCCGAGTAG	80013
rs370744854	in-del	-/TTTATTAGGAGATAATGTCAACTA			intron-variant	FAM188A	GRCh38.p7	10:15821875	AAAACTTAGCATGTA[-/TTTATTAGGAGATAATGTCAACTA]ATCATTACAGTACTG	80013
rs370754417	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15830020	CAAATTTCGAGAATG[C/G]AGAATCTCGAAGACT	80013
rs370768714	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15817293	ACGATAATAACTTTA[C/T]AAGGAAAATAATTAT	80013
rs370832611	snp	A/C	1.66446e-05	0.00288479	intron-variant	FAM188A	GRCh38.p7	10:15841610	TTCCTCTAAAAATAA[A/C]CAAAGCATAAGTTAT	80013
rs370914075	snp	A/G/T			intron-variant	FAM188A	GRCh38.p7	10:15842287	CTGTCTCTCCTAATG[A/G/T]ATTAACAGTTCTTTA	80013
rs371008380	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15789044	AGGACAGTAATTGCT[A/G]GGTGGGAAAGGAAAC	80013
rs371026919	snp	C/T	0.00013079	0.00808567	intron-variant	FAM188A	GRCh38.p7	10:15841389	ATTAAAACAAAGGAA[C/T]AAGAAAAAAACTTCA	80013
rs371064636	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15802244	TTATGTTTTCAAAAA[C/T]GAACTGCATTAGTCT	80013
rs371066293	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15805471	TTCAAAGTTAGGACT[C/T]TTTGTATCACTGGAA	80013
rs371078393	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15854195	ATTTCGTATTGCAAC[G/T]AATCTCTACAATACT	80013
rs371111421	snp	A/G	8.28892e-05	0.00643721	synonymous-codon, nc-transcript-variant	FAM188A	GRCh38.p7	10:15834596	TGCATCTTCAATTTC[A/G]TTTTTTATGTTTTCA	80013
rs371173416	in-del	-/A	0	0	intron-variant	FAM188A	GRCh38.p7	10:15789328	CATTATCTAGGGGGG[-/A]AAAAAATCAGAAACA	80013
rs371177841	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15822803	AGTTATGGAAGTGGG[C/T]AAGTCAGAACAGACA	80013
rs371220359	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15804611	GCTTGCAGACAACAT[A/T]TTATAGTGTTTAAAG	80013
rs371276727	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15858380	ATTTAGAATAATGAT[C/T]AGCCATCAAATAAAC	80013
rs371300504	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15846499	TTCCATAATTCCAAG[A/G]CAAGATTCAGACATT	80013
rs371358627	in-del	-/CA			intron-variant	FAM188A	GRCh38.p7	10:15822341	GTCTCTCTGTACACA[-/CA]CACACACGGAGTGGT	80013
rs371376516	snp	A/T			utr-variant-3-prime, nc-transcript-variant	FAM188A	GRCh38.p7	10:15778250	TAATGTAATAACAGA[A/T]CTTCTCATGCATTTA	80013
rs371382624	snp	A/C/G	0.00199481	0.0315187	intron-variant	FAM188A	GRCh38.p7	10:15835057	CATTAAATAATTTGC[A/C/G]TTTTAATTATTTAAC	80013
rs371403797	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15812421	TACAGCTTCTGATAT[C/T]TTACTCTATCTTAGC	80013
rs371471769	snp	A/C	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15828885	AGAAAAATTACAATT[A/C]AATAGTTACTCGTTG	80013
rs371510646	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15854134	CAAGACAGACCAATG[C/G]ATTTCAATTTAACAG	80013
rs371541729	snp	C/T	1.93392e-05	0.00310954	intron-variant	FAM188A	GRCh38.p7	10:15833747	AATTAAATATGAATA[C/T]AGTTGCCAAATCAAA	80013
rs371634523	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15791778	GTGAGGCATGTAATT[C/T]CCTGGATAAGATAAC	80013
rs371644829	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15846131	CCTGGCCGTGATTCT[C/T]AAACTTAATTACTAC	80013
rs371686980	snp	A/C	0.0232847	0.105357	intron-variant	FAM188A	GRCh38.p7	10:15818308	TGTGTATTTAAATTA[A/C]GGTAGAAGTAAAAAA	80013
rs371696730	snp	A/T			utr-variant-3-prime, nc-transcript-variant	FAM188A	GRCh38.p7	10:15778558	TAGAAAAATGAACTC[A/T]TCTGCATTTCATTGT	80013
rs371725801	snp	A/G	3.53832e-05	0.00420599	intron-variant, downstream-variant-500B	FAM188A	GRCh38.p7	10:15782135	CAGTTGAACACCGAC[A/G]ACTACGTGAATTATC	80013
rs371796342	snp	G/T	2.80769e-05	0.00374669	utr-variant-5-prime, missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15860299	TAGTCAGTTCGGACA[G/T]GATGAGGAACCGGCG	80013
rs371814494	snp	A/C/T	3.36492e-05	0.00410167	intron-variant	FAM188A	GRCh38.p7	10:15816793	TATAATACTTGTTTG[A/C/T]CTGATGTCATAACTT	80013
rs371827017	snp	A/G			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15784644	CAGGAGGCTGAGGCA[A/G]GAGAATTGCTTGGAC	80013
rs371830651	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15824278	CTTTTCTCTATCTTC[A/G]CCACACTTTTGTTGT	80013
rs371839366	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15819111	AAGAGATTATTTCAT[C/T]ACCTTAATTGTATTA	80013
rs371863382	in-del	-/A			upstream-variant-2KB	FAM188A	GRCh38.p7	10:15860549	AACTCCCGCCCCTTA[-/A]GGCTGAGGGCCCGGA	80013
rs371930915	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15807861	GCTGCATAAGGCAAA[C/G]AGTACATAAGGGTAA	80013
rs371955391	snp	C/T	0.000134932	0.00821267	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15779186	AAGCAACAGTCTTAG[C/T]AAATTCTTATGTGGA	80013
rs372006386	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15856352	CAAAAATTGTGCTAC[A/G]CTGAAAGCCCAAAGC	80013
rs372025588	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15803853	CACAAAAAACCCCAC[A/G]AATGATAATTAAGTA	80013
rs372042298	snp	A/C	0.000116309	0.00762502	intron-variant	FAM188A	GRCh38.p7	10:15834521	AGTTCACATGAGGAG[A/C]CAAGAGATTTTAGTT	80013
rs372073617	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15830432	TGTTTAATTCCACAC[A/G]GTTTAATAAATGGCG	80013
rs372128614	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15791971	TGTTGGATACTCAAA[A/G]CTAACAGAGAAGCTG	80013
rs372181163	in-del	-/ATCTT			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15785724	TTTCTTAACAATTTT[-/ATCTT]GAGTTTAACAATCTT	80013
rs372262739	snp	A/G	0.000153988	0.00877328	intron-variant	FAM188A	GRCh38.p7	10:15860187	AGCGGCTGCAAGTGT[A/G]AGAGCCCCGCCAGGG	80013
rs372265769	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15800251	TACCATGAAATGCCA[C/T]AAATCTATTATAAAA	80013
rs372317786	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15810662	TATTTGGTCAACAAA[A/G]AGTCATTGAGCACCT	80013
rs372317948	snp	C/T			intron-variant, downstream-variant-500B	FAM188A	GRCh38.p7	10:15782447	AGTAGGGAAGGTTGA[C/T]TTCCATTATAAGCTC	80013
rs372329226	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15850692	AATGCCGGCCCAGTA[A/C]AACATGAAACTTCAT	80013
rs372367173	in-del	-/C			intron-variant	FAM188A	GRCh38.p7	10:15831673	AAGGAGCCTCCTTTT[-/C]TTTTTTTTTTTTTTT	80013
rs372385549	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15797271	ACCTGTGCAAGCCCT[G/T]ACAAGTTTTTCATGT	80013
rs372425699	snp	C/T	1.66579e-05	0.00288595	missense, downstream-variant-500B, nc-transcript-variant	FAM188A	GRCh38.p7	10:15779047	TCAATGTATGGCCAT[C/T]TGGTTTGCAGACAGC	80013
rs372449585	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15826212	TTTTAAGTGCGTAGG[A/G]AAGCCAGCCATCGAA	80013
rs372473285	in-del	-/A	0.0667418	0.170048	intron-variant	FAM188A	GRCh38.p7	10:15786687	AGTGGATACCAGAGG[-/A]AAAAAAAAAGCTGCT	80013
rs372496536	snp	A/G	1.69241e-05	0.00290891	intron-variant	FAM188A	GRCh38.p7	10:15838315	TCAGCACTACACATG[A/G]CAAATAAATGACACA	80013
rs372526674	snp	C/T			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15784913	GACACCGAGGGCGTC[C/T]GAGCTGCTATAGGAT	80013
rs372560369	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15794139	CAGTGTCCTTCTAGG[G/T]CAGTTATTCTAAAAG	80013
rs372578014	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15826885	TCATAAATACAAAAT[C/T]CAGATAGACTAAAGA	80013
rs372586893	in-del	-/AT	0.00557542	0.0525036	intron-variant	FAM188A	GRCh38.p7	10:15825032	ATTTAATATTCTCAC[-/AT]GTTACGATTTATAGA	80013
rs372591994	snp	C/T	0.000153988	0.00877328	intron-variant	FAM188A	GRCh38.p7	10:15834531	AGGAGACAAGAGATT[C/T]TAGTTAATTACCTGC	80013
rs372665944	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15852532	AGCAAAGGAGACTGA[A/T]AAACATTAGAAGGAT	80013
rs372752445	snp	A/G	0.000798403	0.0199641	intron-variant, downstream-variant-500B	FAM188A	GRCh38.p7	10:15782422	GTTGCCTCTGAAGAA[A/G]ATGCTGGAAAGTAGG	80013
rs372760229	snp	C/T	0.000437904	0.0147905	intron-variant	FAM188A	GRCh38.p7	10:15796039	ATAAAATCAGGTCGC[C/T]ATCAATGTATTTCAA	80013
rs372769791	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15821878	GAGCAGTACTGTAAT[A/G]ATTACATGCTAAGTT	80013
rs372810709	in-del	-/TA			intron-variant	FAM188A	GRCh38.p7	10:15781401	CTAATACATATATAT[-/TA]TATATATATATATAT	80013
rs372823116	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15850969	ACCTACGTTGAAATA[C/T]TGGGTGCTGGTTCCC	80013
rs372869145	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15788258	AGTTCAACACTCTGA[A/T]TTTCTCTTTAAATTG	80013
rs372893581	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15832211	CAGTGTGGGAAGGGT[A/C]AGGCCAGAGCACACA	80013
rs372902083	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15839700	AGGTAAAATAGATTG[C/T]TACACGGAATAAAAA	80013
rs372908244	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15851777	TAGAAATGGAAATCA[C/G]ATTTTGACACAGCCT	80013
rs372932934	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15800955	CAAGCTAAAGCAAAA[C/T]AAAAGTAAAGGAGCT	80013
rs372954528	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15832832	AGAAAAATTCAAATG[C/G]AAGATCATGAATCAC	80013
rs372964594	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15794735	AAGAAAATAAATAGT[A/G]CAAGCCTGCTACCTC	80013
rs372973865	snp	C/T	4.97154e-05	0.0049855	utr-variant-5-prime, missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15841590	CAAAGGAGTTCCTTC[C/T]GCTCTTCCTCTAAAA	80013
rs372994140	in-del	-/A			intron-variant	FAM188A	GRCh38.p7	10:15856418	CCCCTGGGGAAAAAG[-/A]AAAAAAAAAACCCAC	80013
rs373037872	snp	C/T	0.00279162	0.0372561	intron-variant	FAM188A	GRCh38.p7	10:15827111	GACAGAGCGAGACCC[C/T]GTCTCTAAAAAATGA	80013
rs373045658	snp	C/T	0.000176106	0.009382	intron-variant	FAM188A	GRCh38.p7	10:15789202	TGTCTTAAACTTAAT[C/T]GAATCTTTTTGAGTT	80013
rs373051591	snp	C/T			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15786201	GGCTTCTACTACCCA[C/T]AGCCACCTTGACCTC	80013
rs373064923	snp	C/G	0.00835141	0.0640778	intron-variant	FAM188A	GRCh38.p7	10:15853767	GAGTGCTGCTTTTAC[C/G]TAGTATAACTACCAA	80013
rs373084574	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15792760	ATATAATTGTACAAG[A/G]GGGAGGGGATAAAGG	80013
rs373088722	snp	C/T	0.00358779	0.0422022	intron-variant	FAM188A	GRCh38.p7	10:15802037	ACATATTCTTTTCTC[C/T]GGCTTACGAGATTAC	80013
rs373125107	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15787882	AGGATGGCCCAGTTA[C/T]TTCATGGGCCATTCT	80013
rs373132224	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15808669	GTTTCTTTATATGAA[C/T]AGTTCTGTCATGGAT	80013
rs373132472	snp	C/G			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15779257	TAGTTTCAGATGAAA[C/G]TTGACATGTAATTTT	80013
rs373155182	snp	A/G	0.0252325	0.109451	intron-variant	FAM188A	GRCh38.p7	10:15836105	TCTTTTCTTACATAT[A/G]TGCCCAGTCTCATCT	80013
rs373196502	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15807684	TCCATCAGTATTTTA[C/T]CTTTAGACAATTATT	80013
rs373210343	snp	A/G			upstream-variant-2KB	FAM188A	GRCh38.p7	10:15860896	TGTAGGGCGCTTCTC[A/G]TAAGCTGGAGGCTGT	80013
rs373241759	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15849316	AGCTAAAGGGTAGTA[C/T]GGGGGTAGGATGGAG	80013
rs373247788	in-del	-/TTTTCTATTCTTAAACCTC			intron-variant	FAM188A	GRCh38.p7	10:15790276	CTATTCTTAAACCTC[-/TTTTCTATTCTTAAACCTC]ATAAGGAGCTGTTTA	80013
rs373289536	snp	A/T	0.000153988	0.00877328	intron-variant	FAM188A	GRCh38.p7	10:15843309	ATTAGTGAAATGCAT[A/T]ATAACCATACATCAT	80013
rs373308163	snp	C/G	0.0107246	0.0724382	intron-variant	FAM188A	GRCh38.p7	10:15828896	AATTAAATAGTTACT[C/G]GTTGAAAATCCTTAG	80013
rs373365194	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15790389	GCAATTTTTTAAGTG[A/G]AGGGTTTAGAGTAAT	80013
rs373366838	snp	A/G			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15786123	GGAAGACATGTCCCA[A/G]TGGGAAACGGCCCAG	80013
rs373456893	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15809191	GAAAACGATGGTTAG[G/T]GAGAAAATAGAGGAC	80013
rs373459366	snp	G/T	0.00716266	0.059414	intron-variant	FAM188A	GRCh38.p7	10:15805516	CACCTAGTGATACAA[G/T]GTAATCGATGGTGGT	80013
rs373586165	snp	A/G/T	0.000153988	0.00877328	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	FAM188A	GRCh38.p7	10:15778957	CTTCTTTCAACATCT[A/G/T]TTATTAAGATCTTCC	80013
rs373630441	snp	G/T	0.000437904	0.0147905	intron-variant	FAM188A	GRCh38.p7	10:15848000	AAGTAGCAGCTAAAA[G/T]AATCTTTCATGTACT	80013
rs373679443	snp	A/G	0.00438332	0.0466095	intron-variant	FAM188A	GRCh38.p7	10:15798028	TTTATGCAGAGGGGA[A/G]CTTACAGGGGCACAA	80013
rs373689732	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15850321	CACCCAAAAGCAACA[A/G]GATGGCTGCAGTGTT	80013
rs373697047	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15833862	TCAATTTTATATATT[C/T]GGCCTTGCTAAATGT	80013
rs373701001	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15831055	CTGAAAAAAGACAAC[C/T]TGAGATTCTAAAGTC	80013
rs373702805	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15840531	AGATAATACTATATG[G/T]AAAGCAAAATGTGTA	80013
rs373728976	in-del	-/TCTTTA			intron-variant	FAM188A	GRCh38.p7	10:15803737	AAACATGCTACTCTA[-/TCTTTA]CTTCCAAGAATCTTA	80013
rs373767536	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15836175	CTCAACTACTTAGAG[C/G]TCCCCAAACCTGCAT	80013
rs373783020	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15818660	TTTGCTCATAAAAAG[A/G]AATGAAATACTAACA	80013
rs373802613	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15854521	GGGACCTGAGTTCCA[A/T]AAACTTGAGAGCCAC	80013
rs373849194	in-del	-/AG			intron-variant	FAM188A	GRCh38.p7	10:15836485	TAGTCCCTAGCATAG[-/AG]TCAATCAACGCTCAA	80013
rs373849835	snp	G/T			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15780493	TTTTCACAAAGAACT[G/T]CATGTACTCATGTCA	80013
rs373863643	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15836981	GACAGCATTTCACAA[C/T]CAGAACATTATTGAT	80013
rs373951119	in-del	-/GAAA			intron-variant	FAM188A	GRCh38.p7	10:15821327	TCGTTAGGTAATAAA[-/GAAA]CAGTGCTTTCTTCAT	80013
rs374083055	in-del	-/C			intron-variant	FAM188A	GRCh38.p7	10:15824300	TTTGTTGTTTTTTAA[-/C]CAGCCATTCTGACTG	80013
rs374105430	snp	A/G	1.66424e-05	0.0028846	intron-variant	FAM188A	GRCh38.p7	10:15816925	ACCAACCTAGAACAA[A/G]TGTAGCAAAATAAAA	80013
rs374161706	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15853617	TAAAAATATATTCTG[C/T]GGAACAAAATGGAAG	80013
rs374227414	snp	A/G	5.89791e-05	0.00543011	intron-variant	FAM188A	GRCh38.p7	10:15833752	AATATGAATATAGTT[A/G]CCAAATCAAATAATT	80013
rs374228627	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15788801	AAAGTTTCAGGTCAG[G/T]TAATTTAATCATTTA	80013
rs374233796	in-del	-/A			intron-variant	FAM188A	GRCh38.p7	10:15800664	AAGAAACCAAAGTCA[-/A]GGACGTAAGAAAAAG	80013
rs374280221	snp	A/G	3.32292e-05	0.00407597	missense, downstream-variant-500B, nc-transcript-variant	FAM188A	GRCh38.p7	10:15779063	TGGTTTGCAGACAGC[A/G]TTTAATAGGAGTGTC	80013
rs374328925	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15810579	ACCTCCCGACCCCCA[A/C]CTTATCAAGTAATAA	80013
rs374331409	snp	C/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15849712	GGAGAGGGTGCCAGA[C/G]AGGGTGCCATTCCAT	80013
rs374348875	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15796524	AAACAAAACCCAAAC[A/C]ATTTTTTCCACATTT	80013
rs374357850	snp	A/G	0.00011698	0.00764697	synonymous-codon, nc-transcript-variant	FAM188A	GRCh38.p7	10:15789303	TTCCAGAAGTGAATC[A/G]GGTATGAATCCATTA	80013
rs374399428	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15791368	AGAGAATAAGGAAAC[A/T]GAGGCACAAAGATGA	80013
rs374434230	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15817428	TCCTGTTATTTGACT[C/G]TTCATGATAGAAGGT	80013
rs374438383	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15845691	TTTTTTTTTTTTTTA[A/G]AGCAGGGGTCTCACT	80013
rs374453869	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15789958	CACACAAAGTCCTTG[G/T]GGGGTAGTTTGAAAT	80013
rs374459280	snp	A/T	1.67545e-05	0.0028943	missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15789256	GCTTACTATTCAGGA[A/T]CTGAAACAAGGTCCA	80013
rs374576156	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15809452	TTTCAAGTAACCTCA[A/G]TGAAAGTGCCATGAT	80013
rs374623464	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15786823	TAATTTGCCAAACTT[A/G]GTTATTTTTAAACTA	80013
rs374654897	snp	C/T	1.67694e-05	0.00289558	missense, downstream-variant-500B, nc-transcript-variant	FAM188A	GRCh38.p7	10:15782202	TGTAGTGGTAGACAG[C/T]AAAAGATTCTGGACC	80013
rs374720506	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15810682	ATTGAGCACCTACAC[G/T]ATGCCTGGCACTGCT	80013
rs374790494	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15826480	ATCTAGTTGGGAAGA[C/T]AATATGTAAAGATAT	80013
rs374797227	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15831927	GTGATCCATCCACCT[C/T]GGCCTCCCAAAGTGC	80013
rs374813806	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15805322	CCAGCCAACTCACTG[A/T]ACACAGGCCTTATAA	80013
rs374880102	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15852737	AGGTTGAAGTGTAAT[A/T]CGGATTAGAAAGAGA	80013
rs374883099	snp	A/G	1.81158e-05	0.00300958	intron-variant, downstream-variant-500B	FAM188A	GRCh38.p7	10:15782121	TTATTTCATCAACCC[A/G]GTTGAACACCGACGA	80013
rs374909645	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15829643	AGAGAAATAACCTAA[C/T]AGGACGTGTAAAATA	80013
rs375031264	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15836488	TCCCTAGCATAGAGT[A/C]AATCAACGCTCAAAA	80013
rs375033416	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15805149	CCAAATTATCGTAAT[C/T]GACCAACTAACTTTA	80013
rs375044749	snp	A/G	6.97593e-05	0.00590549	intron-variant, downstream-variant-500B	FAM188A	GRCh38.p7	10:15782141	AACACCGACGACTAC[A/G]TGAATTATCATACCT	80013
rs375058168	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15799815	ATGGTTAAACATCCA[A/T]GTAGAATACATGGAG	80013
rs375064771	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15825521	CAGCCTAACTGATTA[A/T]CTTATATAAAAGAGA	80013
rs375068079	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15850582	CTGTAGCGCCCCCAG[C/G]CTTATTAGGATTAGG	80013
rs375119225	snp	C/T			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15784723	GCCTGGGTAAAGGAG[C/T]GAAACTCCATCTTAA	80013
rs375156250	in-del	-/A			intron-variant	FAM188A	GRCh38.p7	10:15839638	GGGATGGTGAAAAAA[-/A]TATAAAACACAAGAA	80013
rs375176649	snp	C/T			upstream-variant-2KB	FAM188A	GRCh38.p7	10:15861219	AAAAGAGGGCTTGTA[C/T]TGCCCGAGCTTTGAA	80013
rs375208048	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15808540	AGTAATAAAAGCAGC[G/T]TGTGCTGTAGAAATA	80013
rs375229954	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15787623	ATGTTTTAAGGTTTA[C/T]GAAAGCTGCATCTGC	80013
rs375267120	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15816288	AAAAAAAATGAAAAA[A/G]AAAAAAAATAAAAAA	80013
rs375286627	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15806793	CTATTCCCCAAACAC[A/G]GTATTAACTTTCCCA	80013
rs375313366	snp	A/C			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15780041	AAAAGAAACAGATAC[A/C]GACGACTGTCTTCTT	80013
rs375333983	in-del	-/TT	0.0146672	0.084371	intron-variant	FAM188A	GRCh38.p7	10:15842480	TCTTCTCTACTAAAA[-/TT]TGTTTTGTATTTCAC	80013
rs375352408	in-del	-/T	0.00597247	0.0543191	intron-variant	FAM188A	GRCh38.p7	10:15812702	CTCCACATGCCTGTC[-/T]TGAGAGGTACCTCTT	80013
rs375428340	in-del	-/G			intron-variant	FAM188A	GRCh38.p7	10:15798713	TGAACCTGTGAGGCG[-/G]AGGTTGCAGTGAACC	80013
rs375467247	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15784825	AAAAGGAGTGTTGAG[C/T]CACTATGCATTTTGT	80013
rs375470235	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15829181	AGGAGAAAACTTTTC[C/G]TGCTGTCGGGGTTAA	80013
rs375556134	snp	G/T	0.000153988	0.00877328	intron-variant	FAM188A	GRCh38.p7	10:15860201	TGAGAGCCCCGCCAG[G/T]GTACCTTGCGTCCAG	80013
rs375568228	in-del	-/A			intron-variant	FAM188A	GRCh38.p7	10:15788085	TTTGGAAAAAAAAAA[-/A]CTTTCTTCTTTCTCT	80013
rs375583831	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15797366	TAATGCACAGTTGTC[C/T]CTCATTTACCATCCC	80013
rs375603454	in-del	-/A/AA	0.494024	0.235452	intron-variant	FAM188A	GRCh38.p7	10:15828578	AATAAAGCTATAAGT[-/A/AA]AAAAAAAAAAAAAAT	80013
rs375616136	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15856105	AAAAAACTTTTAAAC[A/G]ATGTGATCCACAGTA	80013
rs375690530	snp	C/T	0.000437904	0.0147905	intron-variant	FAM188A	GRCh38.p7	10:15821593	GTCAGAGGAACAAAA[C/T]AGTATCCACAATAGT	80013
rs375693746	snp	A/G	8.27315e-05	0.00643109	intron-variant	FAM188A	GRCh38.p7	10:15843177	TCTATTAAAACAGAG[A/G]AGGAAGCAAAAGTTT	80013
rs375700628	in-del	-/T			intron-variant	FAM188A	GRCh38.p7	10:15811100	TTTGATAATGCAAAT[-/T]GAACACGGGCCACAA	80013
rs375716036	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15842731	CTTGTTATTATAAGG[C/T]GGCACCACACATCTC	80013
rs375788992	snp	G/T	6.6154e-05	0.00575088	intron-variant	FAM188A	GRCh38.p7	10:15843299	TAAAGCAATAATTAG[G/T]GAAATGCATTATAAC	80013
rs375802658	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15813001	TGTACTCTTTGCTTA[A/C]CTGAAATAGAACTAG	80013
rs376002241	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15794871	CCTTACAACATCAGC[C/G]TTCTAAAGTTTAGGG	80013
rs376157698	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15833139	GCCACAGGAAAGAAA[C/T]AATTGAGACCAGAAA	80013
rs376178874	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15817014	TAAAGTGTCCAATTT[A/G]TATTTAACTGAAATA	80013
rs376194090	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15842161	AAAATGGCGCAAATG[C/T]TCAGACCATCTCTTT	80013
rs376271485	in-del	-/ATT			intron-variant	FAM188A	GRCh38.p7	10:15844559	CAAAGTTTACTTATT[-/ATT]TAAATTACATTATTG	80013
rs376315769	snp	A/C			utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	FAM188A	GRCh38.p7	10:15778901	AGTTAATCAGTGATA[A/C]CAGTGTTTAGCTTAA	80013
rs376327662	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15789001	TTTAAAGTTTATAGA[A/G]AGACACTTTTAGCAT	80013
rs376385358	snp	A/G	0.000153988	0.00877328	missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15834591	TCACTTGCATCTTCA[A/G]TTTCGTTTTTTATGT	80013
rs376408012	snp	C/T	0.00438332	0.0466095	intron-variant	FAM188A	GRCh38.p7	10:15849741	ATCCCATCTCCTCTC[C/T]TTATCTTCAATCTCT	80013
rs376411813	snp	C/T			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15780101	TCACTGGCTGATACA[C/T]ATGAGTGTAATTATG	80013
rs376445529	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15844850	AAAAAGTAAGAAATA[A/G]AACCTAGTTACAGTT	80013
rs376495047	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15852097	ACAAACCTATCTAAG[C/T]AGTCTCTCCTGTCAT	80013
rs376552122	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15850822	AACTTGCTGGTTTTG[C/T]GGCTCAGGGGGCATC	80013
rs376572509	snp	A/G	0.00112045	0.0236425	utr-variant-5-prime, synonymous-codon, nc-transcript-variant	FAM188A	GRCh38.p7	10:15860222	TTGCGTCCAGCGGCA[A/G]AAAATGGTGTCCGAG	80013
rs376669438	snp	C/G/T	9.92087e-05	0.00704241	utr-variant-5-prime, missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15841489	TAGCAGTTTCCTCAG[C/G/T]TGTCTTTCCTCTTAA	80013
rs376738580	snp	C/T	3.31884e-05	0.00407346	utr-variant-5-prime, synonymous-codon, nc-transcript-variant	FAM188A	GRCh38.p7	10:15841598	TTCCTTCTGCTCTTC[C/T]TCTAAAAATAACCAA	80013
rs376843885	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15828168	ATTACTCATAATGGC[C/G]AAGTGGAAACACTCC	80013
rs376850280	in-del	-/TGAAAAAG			intron-variant	FAM188A	GRCh38.p7	10:15816281	AAAAAAAAAAAAAAA[-/TGAAAAAG]AAAAAAAATAAAAAA	80013
rs376880562	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15834491	TTTATCTGAAGTCAA[A/G]TTTCTAAAAACTGGA	80013
rs376883214	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15796589	AGTTTTCAAATATTC[A/G]AAAATAAAATCCAGA	80013
rs376896768	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15842904	AGCTAAATAAGACTA[A/C]AAAAAAAAAAAAAAA	80013
rs376952449	in-del	-/C			intron-variant	FAM188A	GRCh38.p7	10:15849461	GTTTTTTTTTTTTTT[-/C]TTTTTCCTTTTTTAA	80013
rs376965388	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15802355	AGCTGGGGAGGCTTC[A/G]GGAAACTTATAATCA	80013
rs377050397	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15789933	TCTGATGATGCAACA[C/G]ACCATGACACACACA	80013
rs377055467	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15794616	AATACAACAAATTTT[C/T]ATATGCATCTCTCAC	80013
rs377063659	snp	C/T	0.00358779	0.0422022	intron-variant	FAM188A	GRCh38.p7	10:15819247	ACACAAGCTCAATGA[C/T]TTCCTTAATGCCATT	80013
rs377125608	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15816175	CTGAAGTGGGAGAAT[C/T]GCTTGAACCCAGGAG	80013
rs377181594	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15848184	CAGGAACTCCTCTAG[A/G]AGGATAAAGTATGGA	80013
rs377193908	snp	C/T	0.000119684	0.00773483	intron-variant	FAM188A	GRCh38.p7	10:15821756	AACAACAACAAAAAA[C/T]GAAAACTTAGCATTG	80013
rs377243258	snp	A/G	1.65351e-05	0.00287528	synonymous-codon, intron-variant, nc-transcript-variant	FAM188A	GRCh38.p7	10:15786596	GAAGAAATGGGCCCA[A/G]TAATATGATTCCTAA	80013
rs377302241	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15834338	AAACAAAATATTTGC[C/G]CCAATAAATGCATAC	80013
rs377402783	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15830896	GTCGTTACACATCAC[A/G]ATTTTTGTTTTAGGC	80013
rs377435612	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15793191	TCTTCCACAAAAAAG[A/G]CACACAAAAATAAAC	80013
rs377441731	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15808107	AATAATTAAGCTGTC[C/T]AGATGTCTACCCAGA	80013
rs377470009	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15861061	AATTCAGAGCAACCT[A/G]TTTGTAAATGTTACA	80013
rs377473887	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15808690	TGTCATGGATATTCA[C/T]GTGTTCATGCCTGAC	80013
rs377474977	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15795073	CATAACGATTACATG[A/G]AAGCCATGTGTTTGG	80013
rs377505353	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15829561	CGAACACAGAGGCTC[C/T]TGAATGCTAAGAAGC	80013
rs377527750	snp	A/C	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15790609	CCACCAACAGACAGG[A/C]ACAATTAGGTTTCTG	80013
rs377532693	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15810505	TCTATTTGCCCTCCA[C/T]GTAAGATAGAGATCT	80013
rs377568694	in-del	-/C	0.0387552	0.1337	intron-variant	FAM188A	GRCh38.p7	10:15818330	AGTAAAAAAAAAAAA[-/C]AAACAAACAAAGGAT	80013
rs377568966	snp	A/G	0.000101897	0.00713709	missense, downstream-variant-500B, nc-transcript-variant	FAM188A	GRCh38.p7	10:15779012	TTAGTGAAGGAGAGC[A/G]ATCTGTGGTCCAGAG	80013
rs377603697	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15831065	ACAACTTGAGATTCT[A/G]AAGTCAGCTGAGAGT	80013
rs377607359	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15848551	AGGCCGAAGAATGGC[A/G]TGAACCTAGCAGGCG	80013
rs377705947	snp	C/T			downstream-variant-500B	FAM188A	GRCh38.p7	10:15777994	ATGTGGGTTCTCATG[C/T]TTCTGGCTGGCTGAG	80013
rs377734606	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15787343	AGAAGGCAGAAGAAG[A/G]CAGACTGCAGTTTAA	80013
rs377754195	in-del	-/TC			intron-variant	FAM188A	GRCh38.p7	10:15841653	TGGAAAAAAAAAAAT[-/TC]TGTCATGAATAACAA	80013
rs386741314	multinucleotide-polymorphism	CCG/TCA			intron-variant, cds-indel	FAM188A	GRCh38.p7	10:15783216	TCCAGGAGCACTTTC[CCG/TCA]GTGCTTGCTTCTTCA	80013
rs386741315	multinucleotide-polymorphism	CGT/TGC			intron-variant	FAM188A	GRCh38.p7	10:15800188	AGAAAAAATTAAGTA[CGT/TGC]CATGCATGCATAAAA	80013
rs386741316	in-del	ACA/G			intron-variant	FAM188A	GRCh38.p7	10:15822340	GGTCTCTCTGTACAC[ACA/G]CACACACGGAGTGGT	80013
rs386741317	multinucleotide-polymorphism	CA/TG			intron-variant	FAM188A	GRCh38.p7	10:15830911	GATTTTTGTTTTAGG[CA/TG]GTAGAAGCCACCTAA	80013
rs386741318	multinucleotide-polymorphism	CA/GC			intron-variant	FAM188A	GRCh38.p7	10:15845777	CTCCCAAAGTGCTGG[CA/GC]TTACAGGTGTGAGCC	80013
rs386741319	multinucleotide-polymorphism	CAG/TAA			intron-variant	FAM188A	GRCh38.p7	10:15850330	GCAACAGGATGGCTG[CAG/TAA]TGTTCAGGGAACAAG	80013
rs386741320	multinucleotide-polymorphism	CG/TT			intron-variant	FAM188A	GRCh38.p7	10:15850682	TATCAATGACAATGC[CG/TT]GCCCAGTACAACATG	80013
rs386741321	multinucleotide-polymorphism	AT/GC			intron-variant	FAM188A	GRCh38.p7	10:15856979	CCTCAAACACAGCAG[AT/GC]AGATCAGTCCTTTAA	80013
rs386741322	multinucleotide-polymorphism	CG/GA			upstream-variant-2KB	FAM188A	GRCh38.p7	10:15862291	CAGCAAGTGAGAGAT[CG/GA]GGGAAGTAGTACTGA	80013
rs398012906	in-del	-/T	0	0	intron-variant	FAM188A	GRCh38.p7	10:15848662	TTTAATTTTTCTTTC[-/T]TTTTTTTTTTTTTTT	80013
rs527260405	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15845561	TTGGAGGGCAGTGGC[A/G]TGATCATAGCTCACT	80013
rs527261637	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15804463	ATTCATTACTGAAAA[C/G]GTCTTTAAAGTTTTT	80013
rs527280157	snp	G/T	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15844098	TCCACTATTACTAAC[G/T]AAAAATAACTGTACA	80013
rs527309232	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15798816	AAACCACTATGCCAA[C/T]GTAGAAAGAAATTAA	80013
rs527327857	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15842208	CTCTTTTCAAGCAGT[A/G]TTACTCTCAAGAAGT	80013
rs527415494	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15805732	CTTTAAGTGCCACTA[C/T]CTGGTTTGGCCAGAA	80013
rs527459950	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15860971	TAAAAACATGGCAAA[A/G]AATGTGGCATAATGT	80013
rs527492984	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15819761	TAGTGTGTTTTGTTG[C/T]GCCATTAGCAGAAGC	80013
rs527566674	snp	A/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15831008	ACTCTGGAAAGATAT[A/T]TAGTTCTTCTAAAAC	80013
rs527620550	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	FAM188A	GRCh38.p7	10:15860530	CCACTTCCGACTCCT[C/T]TTTAACTCCCGCCCC	80013
rs527630636	snp	A/C/G			intron-variant	FAM188A	GRCh38.p7	10:15802193	TTGACTATGCAGGGG[A/C/G]TTAGCACCCCAACTC	80013
rs527632404	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15836067	TTTGTACAGTGTACA[C/T]AGAAAGGTCTTCATA	80013
rs527691876	snp	C/G/T			intron-variant	FAM188A	GRCh38.p7	10:15799974	GAAAACTTATGGAAG[C/G/T]AGATTCCTTCAAAGA	80013
rs527693445	snp	A/G	0.00676609	0.0577691	intron-variant	FAM188A	GRCh38.p7	10:15843641	ATTTAGATTCCTTCA[A/G]GTAAAAGAAATCTAA	80013
rs527737977	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15804849	TACCTGAAAGCAGGA[A/G]GGATGGTGGTCTTTT	80013
rs527742364	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15797820	GGGTTATTATTATTC[C/T]TCAGTTCCCTTTATC	80013
rs527750837	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15835458	GGAAACAAAGAAGCA[C/T]GAGCTCTTGCATATG	80013
rs527757007	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15795549	AATAAAGTCTTAACC[A/G]TTACCTAAATATGTA	80013
rs527773884	in-del	-/A	0.00722882	0.0596838	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	FAM188A	GRCh38.p7	10:15778832	ATAAAGCTTTAGGAC[-/A]AATAATTTAAACATA	80013
rs527795576	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15835366	TTGTTTCTATCATAT[G/T]AGAGGTCATTTCTAA	80013
rs527872796	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15848147	GCACGTAAGAGTACA[C/T]ATACTCACACAATTT	80013
rs527912076	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15848565	CGTGAACCTAGCAGG[C/T]GGAGCTTGCACTGAG	80013
rs527927258	snp	A/G			upstream-variant-2KB	FAM188A	GRCh38.p7	10:15862293	GCAAGTGAGAGATCG[A/G]GGAAGTAGTACTGAC	80013
rs527952837	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15859791	TCCCTTGGACGTCCC[A/T]CCTTCTCACCAAAAA	80013
rs527953463	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15852530	TCAGCAAAGGAGACT[A/G]ATAAACATTAGAAGG	80013
rs527974952	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15811354	CATCCTGTATATAAA[C/T]ATACCAAAATATATT	80013
rs528011763	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15812132	TTCTTAGTAGAGATG[G/T]GTTTTGCCATGTTGG	80013
rs528121849	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15789763	AGGAATGTCAGTGAT[A/C]CACTGATACTTAGAC	80013
rs528166093	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15824872	CATGCTTAGACATCT[A/C]GTCTGGATGGTAATT	80013
rs528251782	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15788798	CTAAAAGTTTCAGGT[A/C]AGTTAATTTAATCAT	80013
rs528267882	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15796838	ACAAAAATTGTGTTC[C/T]CTTTGATTCTTTACA	80013
rs528328188	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15802828	AAAAAAAAAAATCAT[C/G]TTTTGCTCTTTTGGT	80013
rs528343811	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15834403	ACAATGCATAATACA[A/T]AGAAGTGCTCAAATC	80013
rs528384830	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15806228	CTTCCTATTGAGAGC[A/G]GTCTATATTTTCCTC	80013
rs528412510	snp	A/G	0.000280299	0.0118352	synonymous-codon, nc-transcript-variant	FAM188A	GRCh38.p7	10:15796110	TTTACCTTCTGGGTC[A/G]TAGGTTTGAAAAACT	80013
rs528503219	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15802027	TATAATTTTAACATA[C/T]TCTTTTCTCCGGCTT	80013
rs528504432	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15847005	TAGGATTACAGGTGC[A/G]AGCCACCGTGCCTGG	80013
rs528528330	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	FAM188A	GRCh38.p7	10:15857935	CAGAAAACTAATGAG[A/G]CTGCAGTTGTCAACT	80013
rs528541493	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15853214	GGGAAAGAGTGATTA[C/T]ATGGAAAAGAGGAAG	80013
rs528641343	snp	G/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15828194	ACTCCACATGTTGGC[G/T]AACAAATGAATGTGG	80013
rs528649268	snp	C/T			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15785761	TTAACAATTACATTC[C/T]GAATTTTAGTAATTA	80013
rs528669545	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15821585	AATGTGCTGTCAGAG[G/T]AACAAAACAGTATCC	80013
rs528690575	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15859029	CGAGAGACCTGGAAT[C/T]CACTCCCAGTTCTAT	80013
rs528713739	snp	G/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15782745	ATTAATTAGTGAAAA[G/T]AGCACTGTGAGAAAT	80013
rs528755679	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15833000	GTTAAATGAATAAAT[A/G]AATGAATTCAGACTG	80013
rs528768909	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15827512	CGTGCCACTGCACTC[C/T]AGCCTGGGTGACAGA	80013
rs528776730	snp	A/C	0.00478085	0.0486577	intron-variant	FAM188A	GRCh38.p7	10:15836184	TTAGAGCTCCCCAAA[A/C]CTGCATTATACCCTC	80013
rs528797894	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15787990	GATTGAATCAATTGT[A/G]CTAACTTCATGATTC	80013
rs528809517	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15839284	CTTTAGCAGTCCAAA[C/T]GTATTAAGTTATTTC	80013
rs528811305	snp	A/C			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15783693	TTCATGTCTTACATT[A/C]CCAACTAAAGCCTAA	80013
rs528833424	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15828962	TCTTCATAACATATG[C/G]AGTAATACTTGCCTT	80013
rs528932537	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15832568	GTTTTTTGTTCACGA[A/G]TTTCACTGTTTAAAC	80013
rs528938595	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15800541	CAGTAAAAAGTGATC[A/T]TAAGCAGTTCTCACA	80013
rs528946165	snp	A/C			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15786357	TGGTGTCTGCGTCAT[A/C]TTCTGCTGCCCTCCC	80013
rs528994887	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15848831	TGGATAACCCTGTGA[A/G]GATCATTTCACCTGC	80013
rs529039377	snp	C/T	0.0023933	0.0345097	intron-variant	FAM188A	GRCh38.p7	10:15793723	CAAACCATCAAAAGG[C/T]TGTTCTCCAAAGAAC	80013
rs529076483	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15850155	ACTTCCCCAATCAAT[A/G]CTCTTATAATTTCCT	80013
rs529078300	snp	A/C	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15845480	AATACAAACAAAATT[A/C]TTTACAAAGTTTACG	80013
rs529114095	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15846884	GCCCACCACCACGCC[C/T]GGCTAGTTTTTTGTA	80013
rs529162368	snp	C/T			utr-variant-5-prime, nc-transcript-variant	FAM188A	GRCh38.p7	10:15860484	GCCAGGTTGGGGCAG[C/T]AGCGAGTTTTCCGTA	80013
rs529169875	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15862231	TAATTACGATTCCAA[A/G]GAACAAAACTTGCCT	80013
rs529175444	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15814968	TCTGACAACAAAATC[A/G]TTTCTTAAACATCAA	80013
rs529190125	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15856175	GTCATTTTATTACTT[C/T]GATAAAATAGTAAAT	80013
rs529229799	in-del	-/AGAGCGCTGCGGGTATTT	0.00874735	0.0655527	intron-variant	FAM188A	GRCh38.p7	10:15859983	GCCCGGAGGATGGAA[-/AGAGCGCTGCGGGTATTT]AGTGGCAGCTGTAAC	80013
rs529247452	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15779332	GAAAGTAAATTTGTA[A/G]ACGATATTTAATTGC	80013
rs529252474	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15820433	CAAGACGCAGGCATG[C/T]GTGCACATCCCACTT	80013
rs529285911	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15861780	AGGTTTTGTTAATTT[A/G]TGCTTTATTACTAGC	80013
rs529313568	snp	C/T	0.00279162	0.0372561	intron-variant	FAM188A	GRCh38.p7	10:15792694	ACATATTTTAGCAAC[C/T]TAACAAAACAAACAG	80013
rs529364378	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15831732	TCAGGCTGGAGTGCC[A/G]TGGCATGATCTCAGC	80013
rs529422959	snp	C/T	0.00318978	0.0398085	intron-variant	FAM188A	GRCh38.p7	10:15799370	TGCCCGGCTAATTTT[C/T]GTATTTTTAGTAGAG	80013
rs529424839	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15792197	TGACCTTTTCCCCAA[C/G]GCCAAGTCACACACC	80013
rs529471923	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15836602	CTATGAGACTGGTAT[C/T]TGGGGAAAAAGAGTA	80013
rs529472044	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15844577	TAAATTACATTATTG[G/T]GCATTAGGTTGCTTG	80013
rs529499108	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15801158	AGGTTTTTAATGTGG[A/T]CAAAGGTGTCCTATT	80013
rs529504826	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15803932	CCTAGTTGTAATACT[C/T]AGGAGAAAATTTCAA	80013
rs529581508	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15798778	GGGCAAGACTCTGTC[G/T]CAAAAACAAACAAAC	80013
rs529618878	in-del	-/T	0.237593	0.249692	intron-variant	FAM188A	GRCh38.p7	10:15832447	GACACTGAAATGAGA[-/T]TTTTTTTTTTCATTG	80013
rs529646521	snp	A/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15848696	CATTGTAGACAGTAC[A/T]TGTGTTTATATTGGC	80013
rs529675041	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15805062	ACGCAGTGGGAGAAG[A/T]AGTTTCCAACAGATG	80013
rs529690245	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15854618	TGAACAGGTGTTATA[C/T]TGAGAGTGAGAGGAA	80013
rs529706334	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime, nc-transcript-variant	FAM188A	GRCh38.p7	10:15860475	GCCTGTCAAGCCAGG[C/T]TGGGGCAGCAGCGAG	80013
rs529729263	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15851334	AGGACTCCAGACATA[C/G]ACAGAGTCTAAGTCC	80013
rs529749418	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15860860	AATAGTTGAGTCACA[A/G]TGCGGTAACATCCGT	80013
rs529754694	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15853688	TCAAAAGTTATCTCA[A/C]GGAAAAGTATATGTG	80013
rs529777062	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15812915	CACCCAGTCCTGTCA[C/T]TCTACCTCAGGAGTA	80013
rs529803120	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15819121	TTCATCACCTTAATT[A/G]TATTAATGCATGTAT	80013
rs529859832	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15784307	CCACTTTTTTCTTCC[C/T]GCATCAGCCTCTACA	80013
rs529862702	snp	C/G	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15830464	AACTGAGATTCCAAC[C/G]ACAGTAGTCTAATTC	80013
rs529880039	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15824067	TCCCTAGCTTTGCTA[C/T]TGTGAATGGTGCTGC	80013
rs529880609	in-del	-/A	0.00716266	0.059414	intron-variant	FAM188A	GRCh38.p7	10:15800663	CAAGAAACCAAAGTC[-/A]AGGACGTAAGAAAAA	80013
rs529910967	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15790301	TTAAACCTCATAAGG[A/C]GCTGTTTACCCATTT	80013
rs529924106	snp	A/C	0.00119737	0.0244387	downstream-variant-500B	FAM188A	GRCh38.p7	10:15777758	CCCAAACAGAAATTC[A/C]CACAGGAACTATACT	80013
rs529986570	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15835992	TCAACAAAAAGATCT[C/T]GTCACTCCCTTGTTC	80013
rs529997696	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15842320	TGCAGGAACTATGCT[A/G]TTCACTTTCTAATCA	80013
rs530054694	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15834724	CAATTATTTAAGTAA[C/G]TTTTCTACCACAAGT	80013
rs530091153	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15797728	ACCAATACAGCCTTA[A/G]CTCTATAATTAACTC	80013
rs530127156	snp	C/G			downstream-variant-500B	FAM188A	GRCh38.p7	10:15777925	GAATACAGCAGATCT[C/G]TCTCTCAAGTAAACG	80013
rs530160782	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15812085	TAGCTGGGATTACAG[G/T]TGCCCAGCACCACGC	80013
rs530226119	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15859300	TTCGGGAACAGGTGT[C/T]CCCTAAATAGATGTT	80013
rs530229824	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15852455	TCAGTTAAAGTGAAT[A/G]AGAACTTGTAAAACA	80013
rs530253497	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15804100	GTTCTTTACATTAGT[C/G]TGATATAATCACATG	80013
rs530267314	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15847578	TATTACTTAATAGGA[C/T]CTCTGTGTTAAAGAA	80013
rs530268231	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15816300	AAAGAAAAAAAATAA[A/G]AAAGACAAGAAAAGA	80013
rs530321969	snp	C/T	0.00199481	0.0315187	intron-variant	FAM188A	GRCh38.p7	10:15823355	ATGTTAATTACCTTT[C/T]TACACTTACTCTCTC	80013
rs530332062	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15853800	AGCTACAGTTATTCA[C/G]ACTTGAGTATCTGGC	80013
rs530336534	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15859133	ACTAAATATCCCAAC[C/T]TAACAATACATCGTA	80013
rs530385828	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15854162	CAGAGGATGAAAAGT[C/T]ACATGATTTGGTTTT	80013
rs530388712	snp	A/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15782487	AACTTATTTTTTTTT[A/T]AATTATGTGCATGTA	80013
rs530391504	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15828952	TCAGTTTCCTTCTTC[A/G]TAACATATGGAGTAA	80013
rs530392247	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15858477	TTAAAATAATATAAA[A/T]ACAGCTACCATATAC	80013
rs530395048	snp	C/T	0.0103295	0.0711199	intron-variant	FAM188A	GRCh38.p7	10:15832586	TCACTGTTTAAACTC[C/T]GACCTTTACTAGAAA	80013
rs530406424	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15819893	GGGAAAAACGTTCTT[C/T]TGTTCTACCTAAAAA	80013
rs530434063	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15851844	AATAAAACCCAAACT[C/T]CTTTCTGTGGTCTAG	80013
rs530483979	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15795956	TGTTCCCATTTTCAC[C/T]ACTTTCCTTTTAAAA	80013
rs530499274	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15828406	GATGAGCGGATGCTA[C/G]GGCTGGCGTGGAAGG	80013
rs530518465	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15857779	TAAAAACAACTATGT[A/G]CCACTCCTGCAGCTT	80013
rs530519716	snp	A/T	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15816574	TCTATAACACAAGTG[A/T]TTTCTGAAAAAAATC	80013
rs530591534	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15788259	GTTCAACACTCTGAA[C/T]TTCTCTTTAAATTGA	80013
rs530638506	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15810447	TCTATTCAATAATAC[C/G]GGTGGTTTGAATTGG	80013
rs530681733	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15846931	GGTTTCACCATGTTA[C/G]CCAGGATGGCCTCCA	80013
rs530690793	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15840089	TTTCTCACATCAATA[C/T]ACAGACTGGCTTTAA	80013
rs530753471	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15801973	CAATGAGGAAGATGA[C/T]GTAGAAGAAGCAGGG	80013
rs530771665	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15840801	TCGGGTCAATTACAT[A/G]ACAATTTTCAAAAGT	80013
rs530773309	snp	A/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15833167	AAATGGAAGTGGTAG[A/T]GGAAGAGTTGGTAAT	80013
rs530785554	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15852989	GAGATTATTTAAAGT[G/T]TAGGGGAAGTCGTGT	80013
rs530806244	snp	G/T	1.65072e-05	0.00287286	intron-variant	FAM188A	GRCh38.p7	10:15796050	TCGCTATCAATGTAT[G/T]TCAAACATATGAAGA	80013
rs530809964	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15857727	TAAAACGAACAGGGA[A/T]TTGTAGAAGAGAATT	80013
rs530826428	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15816191	GCTTGAACCCAGGAG[A/G]CGTAGGTTGCAGTGA	80013
rs530850519	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15846560	CTAATGCAAAAAAAA[C/G]TCAACTTAAAAAAAT	80013
rs530877527	in-del	-/A	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15821436	TGCCCCTCCTCCGAC[-/A]AAAAATAACAACAGA	80013
rs530889248	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15781161	CATTGTCAAGAAAAT[C/T]TGGATGCTGTATATA	80013
rs530949880	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15808269	TATTAGATGAGGCAC[A/G]AAATCTCAATATATG	80013
rs530964735	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15851011	ACCAAACTCATTCTC[A/C]CCCAAGTTCATCAGT	80013
rs530974182	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15780332	CTTTATTTTAGTTAA[C/T]ATATTAGTTTCTAGT	80013
rs530997900	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15787201	AGAGCTAATGCGTCA[C/T]GAATGACAGTGACTG	80013
rs531045877	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15857000	CAGTCCTTTAAAAAC[C/T]TGTCAAGTAGTATCT	80013
rs531093432	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15826958	AAAATACTAGAGAAT[A/G]TTATCTTGGGGTGGA	80013
rs531122242	snp	A/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15782590	ATTTGTTCCTCTCAA[A/T]GAATTGAGAAAAGCA	80013
rs531167159	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15837528	GATATTTATCATTAA[A/G]AAAGAACACCTACTT	80013
rs531170499	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15820182	AAAGTCTCTGAGGTA[C/G]GATCTGCAGTCCAGC	80013
rs531198218	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15793628	GATACTGGTAGTAGA[C/G]AGAAGGGGAAAGATT	80013
rs531215218	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15832169	ACTGATGAGTACCAA[C/G]TGTGAGAGAGAGTGA	80013
rs531232233	snp	A/G			upstream-variant-2KB	FAM188A	GRCh38.p7	10:15860716	TTCTAAACTCCAGGA[A/G]TACCTTCTTCCTCTA	80013
rs531308639	snp	A/G			utr-variant-3-prime, nc-transcript-variant	FAM188A	GRCh38.p7	10:15778497	TGTCAAAGGATCCAG[A/G]TTGACAATGTGTTAT	80013
rs531324541	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15850094	TTACGCCTGTCTTTA[C/T]TGCAATCTCTGAACA	80013
rs531382666	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15838384	AAAACTTTCCCTATT[G/T]CCTTACTCCCTTAAA	80013
rs531431435	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15806305	AAGCTGCACATGGAG[G/T]AATCTCCACATACGC	80013
rs531435002	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15849694	ACACCAGGTGAGAGC[A/G]ATGGAGAGGGTGCCA	80013
rs531442137	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15838882	AATGTTTATTGAGCA[C/T]TTTACTAAGTGCCAG	80013
rs531476580	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15861070	CAACCTGTTTGTAAA[C/T]GTTACAGCATTTTCA	80013
rs531486259	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15826119	TACATGGAATAGTAC[A/G]AAATGAAGATGGATG	80013
rs531506986	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15796570	AAGAAATAAAATATA[C/T]TCCAGTTTTCAAATA	80013
rs531520175	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15854893	AACCAAATTTAAGGT[C/T]CAACCTAGGAACAAG	80013
rs531527485	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15855458	ACTTACCATAAATGG[A/C]CGTTTTTCCTGATTA	80013
rs531536636	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15813561	ACTCAAGGAGAATGT[C/T]CGCCTCCATTAAGAA	80013
rs531543469	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15814241	TCCAGCTTTGTTTTA[A/C]TTTTATTTCAAGGGG	80013
rs531613806	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime, nc-transcript-variant	FAM188A	GRCh38.p7	10:15778596	GATATATTACAAGCC[A/G]GAATCATTCAAACAA	80013
rs531624367	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15801267	GAAAAGGCTACTGTT[C/T]TATGCACATGCAGTC	80013
rs531654777	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15798716	ACCTGTGAGGCGGAG[A/G]TTGCAGTGAACCAAG	80013
rs531703628	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15809944	AACTTAAAATTATAT[G/T]TCTTCATGAAAGAAA	80013
rs531768959	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15849872	CCTCCCAAAGTCCAG[C/G]TAGTCATCTATATAT	80013
rs531774365	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15800639	CCACTAGTGATGCCG[C/G]AAGTTCTCCCAAGAA	80013
rs531855508	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15836113	TACATATGTGCCCAG[C/T]CTCATCTTCCACAGT	80013
rs531881673	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15791823	GAGGAAACCTGAGTT[C/G]GGCTTTCAAAGGAAA	80013
rs531918272	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15804953	GCACCAATCTGTGTC[A/G]TATGGGCAGAGAAAT	80013
rs531976755	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15843827	GTCAACGATGTTACA[C/T]TGGTTATTTGATAAA	80013
rs532019045	in-del	-/AGACTAC	0.00716266	0.059414	intron-variant	FAM188A	GRCh38.p7	10:15792086	CACTGTGGGAGAGGG[-/AGACTAC]AGTTTCTTGGGAATT	80013
rs532056785	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15783626	TTGAGAAGGAATCAT[A/G]TAGTACTACTTTGTA	80013
rs532119215	snp	C/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15859841	AGACAGCTCTGTTAG[C/G]GGGTAAAGATGCGGA	80013
rs532132339	snp	A/C	0.000399281	0.0141238	utr-variant-5-prime, nc-transcript-variant	FAM188A	GRCh38.p7	10:15860342	CTTTGCGGACTCCTG[A/C]CCCGGAACATGGGGA	80013
rs532227791	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15823958	TCCAGTTCCATTCAC[A/G]TATACTGCAAATAAC	80013
rs532265087	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15796919	TCTAAAATGTAGGCT[C/T]CTGTTGTTTACCTCT	80013
rs532318580	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15790217	GGAATTGTACACTAT[A/C]TCTATCAGAAAGGAA	80013
rs532430984	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15841687	GTAAGAATGGGTTAA[C/T]GATGAAAATCAAGCA	80013
rs532446166	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15781874	GGACTAACTACGATG[C/T]TGATTTAGAAACACG	80013
rs532494102	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15841061	CTTTATGAAATCTTC[C/T]GATGTCCAAAAAAAT	80013
rs532561662	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15796292	TTTGAGTTACATTTG[C/T]ATCATAGATGTGTAA	80013
rs532566792	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15822914	ATATATTTGGGTCCA[C/T]AATATATCTAAAAAG	80013
rs532570360	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15803491	TGTACATAAAATGGT[G/T]TAGTTAGAAGGAATG	80013
rs532584581	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15816202	GGAGACGTAGGTTGC[A/C]GTGAGGCGAGACTGT	80013
rs532614091	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15856521	GGAAGAAGGAAAATA[A/T]TTGGAAGAAGGAAAA	80013
rs532673718	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15857996	CCAGAGTTGATGTCA[C/T]ATTAGTAATGCAGCA	80013
rs532688679	snp	A/C	0.000181562	0.00952617	intron-variant	FAM188A	GRCh38.p7	10:15796057	CAATGTATTTCAAAC[A/C]TATGAAGACATAAAA	80013
rs532689095	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15802890	TCAACTCTTTAGGCA[A/G]TAACTCTTAATCACA	80013
rs532724736	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15833071	TCAGCTCTCCTTAAC[A/G]GAATGGATTGGCCAA	80013
rs532821864	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15831928	TGATCCATCCACCTC[A/G]GCCTCCCAAAGTGCT	80013
rs532835336	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	FAM188A	GRCh38.p7	10:15782063	TGGAATAATCTTAGG[C/T]AGCAATTGTACGGGA	80013
rs532844435	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15801794	CTGCTAGAGAACACT[A/G]TGTCCAGATATTGTG	80013
rs532896220	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15854806	AGGACAAATGGAGAA[A/C]TGGAATAGAGAAGAT	80013
rs532930615	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15795345	GATTTTCAGAGAGGA[A/G]AAGAGCAGATCACTA	80013
rs533007283	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15850920	TGTCCCTTTATTTCT[C/T]AGACCAGCCAACACT	80013
rs533010420	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15846459	GCTATAATTACTAAT[A/T]TGTAGTTAAATCTCA	80013
rs533047313	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15835504	ATACAAATCAGGCTA[C/T]GATAATGTCAAGATG	80013
rs533057747	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15815629	AGTTACCTATGATCC[C/G]AGAGATGTTTAACGT	80013
rs533113400	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15839925	CATCTAAATTAGTTA[C/T]TGAAGTACCAAAGGG	80013
rs533167610	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15815196	TAATTGTCAGTTTTT[A/G]TAGTTCACATTGTGC	80013
rs533172027	snp	G/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15801181	GTCCTATTCCGGCAT[G/T]GGGGGGAAATGCCAT	80013
rs533183313	snp	C/G			upstream-variant-2KB	FAM188A	GRCh38.p7	10:15861019	ACCAGCTGCAACGCA[C/G]AATTACAAGGTATTT	80013
rs533184360	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15821530	GGGTGGGGGATAGGA[A/G]GGAAGAAGAGAGCGG	80013
rs533229862	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15856970	ACAGTCTATCCTCAA[A/C]CACAGCAGGCAGATC	80013
rs533248746	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15843386	TCTAATCTTTTGACT[A/C]GTTCTGTAAAGATGT	80013
rs533251898	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15829239	ATTTTAATGGGGCCA[C/G]ATGGAATGAGCAGGA	80013
rs533270658	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15850601	ATTAGGATTAGGAAA[C/T]TCCTGCCTAGTAAAT	80013
rs533331309	snp	A/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15785740	TCTTGAGTTTAACAA[A/T]CTTTTTTAACAATTA	80013
rs533462188	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15797437	AACATTATTTTGCTG[A/G]TAATGTATACGCCCA	80013
rs533614032	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15832136	AGAATCCGGAGAACG[C/T]GTAGAAAGATGAACC	80013
rs533685050	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15837398	AATTTTTAAATTTTC[C/T]TATACATTAAAACAT	80013
rs533789659	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15860062	CAAGGCAGGGCGTGT[C/G]TAGAAAGTCCAGCTT	80013
rs533881547	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15805129	ATGAGTGAGCTGCTG[A/G]CTCTCCAAATTATCG	80013
rs533898476	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15823598	ATGTTTTATTTCTAC[A/G]AATTTAGGAGGTAAA	80013
rs533919394	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15798471	TGCCAAGTGTTTTTT[G/T]TTTTTTTTTAAATAC	80013
rs533945674	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15797567	TTACAAAAAATGCTG[A/T]ATCAAATAAACCTGA	80013
rs533995045	snp	C/G/T			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15784484	GTGAGGTGGCTCATA[C/G/T]CTGTAATCCCAGCAC	80013
rs534113533	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15791509	AAATTAACTACATAG[A/G]TATCAACACAAAAGA	80013
rs534117145	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15841890	GACACTGATCATCAC[C/T]TTCTTAAAACTTTAG	80013
rs534121411	snp	C/T	0.00318978	0.0398085	intron-variant	FAM188A	GRCh38.p7	10:15834191	GGTCCGAGAGGAAAA[C/T]GGGGAATGTTTTTCT	80013
rs534157421	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15834822	TTTCTTTCATGGGCT[C/G]TATATAAACAACACT	80013
rs534200657	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15840999	AGAAACAGCTTGCAA[C/T]GAGGAGAAATGTCCC	80013
rs534221879	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15803101	TTTTTGGATCACTGT[A/G]GAAAATGATCTTTTA	80013
rs534241183	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15857430	TACTGTTTGTCTTCC[C/T]TCCCACCCTACTGAC	80013
rs534246477	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15824182	TGGTAATCCTATTTT[C/T]AGTTTTTTGAGAAAT	80013
rs534256102	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15796427	CATAAATACTTAAAA[C/T]ACTGGGGAAAAACGT	80013
rs534290118	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15809662	TAGAAGTTCTGTGGG[A/T]ACCCTGCTGCTTGAT	80013
rs534303254	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15852006	AAAAATGCTCTTTCC[A/G]CTACTCTCCATATAG	80013
rs534325089	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15810566	CCATCTTAAGCACAC[C/G]TCCCGACCCCCAACT	80013
rs534348498	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15854848	ATTTAATAAGAAAGT[C/G]ACAACTAAGGTTTCT	80013
rs534413903	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15789178	TAAAAAGGCAAAAAA[C/T]GTACAATATGTCTTA	80013
rs534423840	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15797227	AAACCTTATTTATAA[A/G]AAACAGGAATGGGAA	80013
rs534450203	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15788965	ATTTTAAGACGTGGG[G/T]AAGTGTTTGCAGAGA	80013
rs534463279	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15826610	GAATAGATAATGTAG[A/G]AAAGACTATGACAAT	80013
rs534481290	in-del	-/A	0.0667418	0.170048	intron-variant	FAM188A	GRCh38.p7	10:15786686	AGTGGATACCAGAGG[-/A]AAAAAAAAAAGCTGC	80013
rs534487716	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	FAM188A	GRCh38.p7	10:15782149	CGACTACGTGAATTA[C/T]CATACCTTTTCATTA	80013
rs534583807	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15855004	CAAAATTAAGATCTG[C/T]TAAACTTTTCGTGTA	80013
rs534659352	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15858145	ACCCCTCTGATTCAG[A/G]GGCGATAACTTCAAA	80013
rs534738855	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15798532	CCTGTAATCCCAGGA[C/T]TTTGGGAGGCCAAGG	80013
rs534741031	snp	A/G	0.0023933	0.0345097	intron-variant, downstream-variant-500B	FAM188A	GRCh38.p7	10:15782333	CCTTATCCTTTGACT[A/G]GGGACTCATTTGACA	80013
rs534756005	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15851517	TTGATACACCTGCTA[A/C]CCATTTCTCTGGAAA	80013
rs534809123	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15846122	GCCACCACGCCTGGC[C/T]GTGATTCTTAAACTT	80013
rs534836022	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15801362	TAACACCAGCTGCCA[A/G]TCTTTTGGCTGTATA	80013
rs534870301	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15857203	TCCTTAAACAGACCA[A/G]GTGTATTTTCTGTGA	80013
rs534937591	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15862447	AGTGTTTCCACATTT[C/G]ACTTTCTCCATTAAT	80013
rs534939926	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15819302	AATGTAAAATATACA[C/T]AGAATTTGAGAAGTT	80013
rs534991437	snp	A/C	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15780430	CTCTGAAAAGTTATA[A/C]ACAAAGAATATAATT	80013
rs535019186	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15859630	TTTAACCGTGACAGA[C/T]AATAAACCATATAAA	80013
rs535028161	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15856586	CAGCAAACTACAACC[C/T]TCATCTGCTTTCATG	80013
rs535044576	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15840359	AAGGCTTCAAAAGGA[A/G]GCATCATATAGCTGT	80013
rs535053594	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15832814	TACACATTTCTGAAT[A/T]TGAGAAAAATTCAAA	80013
rs535083581	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15845755	TAGGCAATCCTCTTC[C/T]CTCAGCCTCCCAAAG	80013
rs535097903	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15826993	GGCATGATGGTGCAC[A/G]TCTGTAGTCTCAGCT	80013
rs535114859	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15800891	GTTGCTATAGGAAAG[A/G]CACACCTTTAGATTC	80013
rs535154301	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15827095	GCACTATGGCCTGGG[C/T]GACAGAGCGAGACCC	80013
rs535233747	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15818065	ATCACAGTTCCAGAG[C/T]GGACGAGGATTTTAG	80013
rs535257550	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15858776	TTGTAAAATGTTTAA[G/T]AAATGTTAACTGATT	80013
rs535260335	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15844918	ATCCTGATTATTTGG[A/C]TGTAAAGCATCATTC	80013
rs535293247	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15837825	TACTTTGTAATAAAA[A/G]GTTTAAATGCTCTAA	80013
rs535321521	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15821172	TGTCAAAGAGTTTAA[C/T]GTTGTAAAATGCTTG	80013
rs535346979	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15843810	AACTTCCCCTTAAGC[A/G]AGTCAACGATGTTAC	80013
rs535363400	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15820946	AAGACCCTGTCTCTA[C/T]TTAAAAAAATTTTTT	80013
rs535421430	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15786464	CAGTCTCATATCTGC[A/G]CATTAGGACATTGTA	80013
rs535434174	in-del	-/AC	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15818447	TTGGACAACAGTTTG[-/AC]ACTTCCTCAGAAAGT	80013
rs535447300	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15813060	TATCCTTCAATATAT[C/G]CATTCTCCACAATTA	80013
rs535491031	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15820649	CTACTAAAGGAGTAA[A/G]GGCAGGACAAATCCA	80013
rs535554395	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15825737	GTTTTGAAATATGTA[C/T]ACACTGTAGAATGGC	80013
rs535622747	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	FAM188A	GRCh38.p7	10:15778732	AAATGACCAAGTATC[C/T]GAATGCAAAAGTGAT	80013
rs535665775	snp	C/T	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15792350	TTAACATTTGTTACT[C/T]TTAATGATACAAGCT	80013
rs535689994	snp	C/T	0.00199481	0.0315187	intron-variant	FAM188A	GRCh38.p7	10:15825136	GAAATCCGAAATGTT[C/T]CAAGATCTGAAGCAT	80013
rs535797706	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15830224	TTTCTCCCAGTTAAT[A/T]GTGATGTGCAGACAA	80013
rs535818463	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15854957	ACTGAGAATAAGGAA[A/G]GGGACCCTAGTGTTG	80013
rs535907134	snp	C/T	0.00159617	0.0282053	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15860728	GGAATACCTTCTTCC[C/T]CTACGCACTGCTCTG	80013
rs535914779	in-del	-/TACTCTTAAGTCCA	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15792953	CTAATCATATAAAGT[-/TACTCTTAAGTCCA]TTTTACAGATGAAAA	80013
rs535929506	snp	A/C	0.000798403	0.0199641	downstream-variant-500B	FAM188A	GRCh38.p7	10:15778001	TTCTCATGCTTCTGG[A/C]TGGCTGAGTTAGCAG	80013
rs535957931	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15803843	CCACCACACACACAA[A/G]AAACCCCACGAATGA	80013
rs535997098	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15861184	AGTTCATGTGAAAAC[G/T]TATGTTTGTGCTGCT	80013
rs536010318	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15830690	ACAGAGTTAGTAAAT[A/G]AGCCATGCAGTGTGC	80013
rs536025603	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15784559	AGACCAGCCTGACCA[A/G]CAAGGTGAAACCCCA	80013
rs536063279	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15811743	AAAAAAAATAACATA[G/T]GTGCACTTTCTCCTT	80013
rs536114336	in-del	-/T	0.00318978	0.0398085	intron-variant	FAM188A	GRCh38.p7	10:15796705	TCTACATGTCCAGAA[-/T]TTTAATTTTTCTGAA	80013
rs536132511	snp	C/T			upstream-variant-2KB	FAM188A	GRCh38.p7	10:15862088	TGTGTAACTTGCTTA[C/T]GACAATTCCTATCAT	80013
rs536194972	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15859431	GTGTCAGTTGTTTGC[C/T]TATCCAAACTTAAGA	80013
rs536203024	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15829145	GCCGACTGAGGTAAA[C/G]CACCATAGATGATCA	80013
rs536206669	snp	A/G			synonymous-codon, intron-variant, nc-transcript-variant	FAM188A	GRCh38.p7	10:15786603	TGGGCCCAATAATAT[A/G]ATTCCTAATCCTTCT	80013
rs536308507	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15853244	GTTTAAGGTCTCCAA[A/G]TCCTGAAAAAGAGCT	80013
rs536354053	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15842046	CCCAAAGGGATAAGA[A/T]TAATGAGATGAGAGA	80013
rs536356086	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15848325	AAACTTTCTGTCACA[C/T]TCTATAAGCTAATCA	80013
rs536446427	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15847161	ACTTCCAAAGTAACA[C/T]TGTCATTCACAGACA	80013
rs536448021	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15840590	TACGTAATCTCTTTA[C/T]GAAAACTTTCCACAA	80013
rs536509700	snp	C/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15851371	ATGGTCCTGTATTAT[C/G]TGGCTCCTGCCTGCA	80013
rs536527072	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15817412	TTTAAGTATGTAAGT[C/G]TCCTGTTATTTGACT	80013
rs536558893	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15846793	CAGTGGCGCAATCTC[A/G]GCTCACTGCAACATC	80013
rs536643010	snp	C/T	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15816539	AAAGCAATCTAAAAC[C/T]TTAAAATTCAATTGT	80013
rs536698655	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15788670	AAGATCTTAATCTAC[A/C]GAGGAAGTTGTAGAT	80013
rs536723403	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15821796	GTATAAATTTGAAAC[A/G]TACTTATATGTATAT	80013
rs536742107	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15793024	CACAGCTAGTGAGGC[A/G]TAACGGATGGAGCCA	80013
rs536822113	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15787541	TCAGTTTGCCTCTTC[A/G]GTCTGGGTCAGTTAC	80013
rs536851809	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15803023	TTTTCTTCCACAAAT[C/T]AAAACCAGTACATAG	80013
rs536851949	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15795688	ATAGGCTCCAAAGTG[A/C]ATGATTCAGATGATC	80013
rs536883242	in-del	-/CTCT	0.00438332	0.0466095	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15785706	CTTTTTGAATCTTAC[-/CTCT]TTCTTAACAATTTTA	80013
rs536886961	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15827793	CAAAACTCACAAACA[C/T]GTGAAGAGATGATCA	80013
rs536946086	in-del	-/GAA	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15832346	GTCCAGAAACAACTG[-/GAA]GAAGAAGAAAGACGG	80013
rs536969471	snp	A/C	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15839489	ATGAAAATTCTACCT[A/C]ATCTTTTCCAAATTA	80013
rs537009111	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15812632	TTGTCTCCCATCACT[G/T]CTCTTTGGAGGGAAA	80013
rs537013023	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15816020	CCTGTGATCCCAACA[C/T]TTTGGGAGGCAGAGG	80013
rs537055882	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15808495	AAGGCTCTAACAGTT[C/T]ACCGCAGTGTTTTTC	80013
rs537070252	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15851693	TGAGTTTCCAACCAC[A/G]TCTCCCTATTCCTTC	80013
rs537083073	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15840548	AAGCAAAATGTGTAT[C/T]CCATACAATTGAAGT	80013
rs537123168	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15856522	GAAGAAGGAAAATAA[C/T]TGGAAGAAGGAAAAA	80013
rs537141705	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15815263	AATAGCAAAAGCTTT[C/G]AAACTAAATGCAATG	80013
rs537306090	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15861269	ATCTGATTTAAAAAA[A/G]AATACATGCTTTTAT	80013
rs537325081	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15820222	ACAGTGAGCCATCCA[C/T]CTCAAGAGCTGGACA	80013
rs537365715	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15832361	GAAGAAGAAGAAAGA[C/T]GGGAGTGTACAGAAG	80013
rs537441816	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15845653	ACAGGTGTGCACTAC[C/T]ATGTCCAGCTAATTT	80013
rs537479730	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15850099	CCTGTCTTTACTGCA[A/G]TCTCTGAACATAAAC	80013
rs537483771	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15831779	CTCCCGGGTTCAAGC[A/G]ATTCTCCTGCCTCAG	80013
rs537489979	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15838875	CAGAGGTAATGTTTA[C/T]TGAGCACTTTACTAA	80013
rs537552151	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15850293	TGTGTGTTTGAACAA[C/T]ATGAAATTTGGGCAC	80013
rs537554214	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15845152	AGGATACATTTGATA[C/T]ATGGTACAAAATTAT	80013
rs537575283	snp	A/G	0.00199481	0.0315187	intron-variant	FAM188A	GRCh38.p7	10:15823668	AGCCAGGGTATGAAG[A/G]GTATCCACTGCTCAA	80013
rs537586657	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15856143	CACTTTGGAAGAAAA[A/C]TTAATGATGTTGGTG	80013
rs537648283	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15849290	TTTATAAATCAGAGA[A/G]AATTTAACACAGCTA	80013
rs537657304	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15814595	TGTTTTTCTCTTAAC[G/T]CCATGTCTCTAATTC	80013
rs537719598	snp	G/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15826487	TGGGAAGATAATATG[G/T]AAAGATATAATTTCC	80013
rs537761378	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15848774	TAGCGGAAGTTCTTC[A/C]GATGGCCCTGGGTCA	80013
rs537816658	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15825035	TAATATTCTCACATG[C/T]TACGATTTATAGAAT	80013
rs537822834	snp	C/T	0.00119737	0.0244387	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15785308	AATGTCTGTTACAGG[C/T]GAAAGAGAAGGGACT	80013
rs537834155	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15853450	TCCTTAGCATACATC[A/G]AGACAGTAACATCAA	80013
rs537856969	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15812519	CTTTGGCATAAAGAA[C/T]AGATGTGGGTCAAAG	80013
rs537892417	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15798949	GCAAAAATCTCGGTG[A/G]ACTCTAGTTAACATG	80013
rs537927886	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15824268	TAGGAGTTCTCTTTT[A/C]TCTATCTTCGCCACA	80013
rs537968346	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15836878	AAAAAATCAAGAAAT[A/G]GAATCAAGGTCAAAA	80013
rs537984623	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15792325	ACAGTGGTTGACTCA[C/T]AGCTGCTCGTTAACA	80013
rs538016180	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15798892	TGGTTCTGAACAGGC[C/T]ATACAAGCTCACCTG	80013
rs538073792	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15792624	ACAATAGTCCAATTA[C/T]TCTTAAAGATTAAAA	80013
rs538078839	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15841663	AAAATTCTGTCATGA[A/G]TAACAATAGTAAGAA	80013
rs538099249	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15796280	GAGTCAGAAGACTTT[A/G]AGTTACATTTGTATC	80013
rs538232308	in-del	-/T	0.00717694	0.0594724	intron-variant	FAM188A	GRCh38.p7	10:15797326	AAAAACCACTTGACA[-/T]TTTTTTAACATTTGT	80013
rs538257378	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15803764	AGAATCTTATTAAAT[G/T]TATCCTAAGAAAATT	80013
rs538302786	in-del	-/TG	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15781550	GCAGTGAATCACCTA[-/TG]TGCTTTGTCAACGGT	80013
rs538456227	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15790601	TTATGTGGCCACCAA[C/T]AGACAGGAACAATTA	80013
rs538534854	snp	A/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	FAM188A	GRCh38.p7	10:15782259	CTATTAACACTTTAA[A/T]TTATATTTATATCAG	80013
rs538632913	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15847735	TTTATTGTAATTTAC[A/C]TGAGCAAAAGTTAAG	80013
rs538710661	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15818125	ACATAAGGAACCAGA[A/G]AAATACACAGGATCT	80013
rs538718048	in-del	-/A	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15800174	TTTTCAAAAGTTAAG[-/A]AAAAAATTAAGTATG	80013
rs538745191	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15852710	CACTAGGGAGAGTAG[C/G]CAAATTTTAAAAGGT	80013
rs538792552	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15795548	TAATAAAGTCTTAAC[C/T]GTTACCTAAATATGT	80013
rs538844254	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15851235	GCTCCTTTCATTCTA[C/T]ATATTTTTCCTGAGT	80013
rs538875539	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15802859	CTCAGTCATATACTA[C/T]TAACAGCTAATTTGG	80013
rs538884912	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15788946	GATACTAATGTCACA[A/T]AAAATTTTAAGACGT	80013
rs538894729	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15846704	AACAAATTTACTTTG[C/T]AGCCAACAGTTTAGG	80013
rs538898942	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15813010	TGCTTACCTGAAATA[A/G]AACTAGAGAAGTCTT	80013
rs538903973	snp	C/T	0.00398564	0.0444627	intron-variant	FAM188A	GRCh38.p7	10:15822582	CATGATAAATAGTGA[C/T]TAACACAAAGAATTA	80013
rs538915374	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15829112	AAAGAACTATGATGC[G/T]AGGTGTAATAGAATG	80013
rs538947155	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15815930	ATACAGATTATAGTT[A/G]AGATTTAAAAATAGC	80013
rs538954111	snp	C/T	0.00398564	0.0444627	intron-variant	FAM188A	GRCh38.p7	10:15850756	TCACTCTGCCCCCAT[C/T]TGCCTTGTGATATTT	80013
rs539029592	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15856632	ACACCCATACTAACC[A/T]TGGCTGCTTTTGCTG	80013
rs539078911	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15833867	TTTATATATTCGGCC[C/T]TGCTAAATGTATCAC	80013
rs539108371	snp	A/C	0.000355806	0.0133333	intron-variant	FAM188A	GRCh38.p7	10:15821749	AAACAACAACAACAA[A/C]AAAAAACGAAAACTT	80013
rs539122436	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15794847	GCAGCATTGATGAAA[C/T]TTTTTCAGCCTTACA	80013
rs539159891	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15817857	TGGAATTTATTCTTA[C/T]CACTAGGAGGGAAGT	80013
rs539177926	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15806686	TAAATAAATGTGATT[A/T]TTCAAGCTGGTCCTA	80013
rs539202239	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15831925	AGGTGATCCATCCAC[C/T]TCGGCCTCCCAAAGT	80013
rs539218268	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15826406	TCAAGTATATGGATT[A/C]AGGACCATATAATCT	80013
rs539246116	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15809403	CTACTTTTCAAAATA[C/T]ATTTCTTTTTACCTG	80013
rs539249660	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15838639	TAAATCCAAGTAATA[C/T]CATCAGAGCTAACCT	80013
rs539254691	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15839776	ATTTTCAGTTAACAA[A/T]GTATTTCAAATGTAT	80013
rs539277554	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15793893	TACCAGGTTTATGCT[A/C]CAAACGATCAGTACT	80013
rs539296929	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15813708	TGCAACTATTACCAC[C/T]TTCACCGCATAAGGC	80013
rs539314071	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15809783	CTTAGATGCATTTCT[C/G]ACAACCAGACTCCTT	80013
rs539332702	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15796262	GCAGACATAATGACA[C/T]TGGAGTCAGAAGACT	80013
rs539357696	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15845557	CAGGTTGGAGGGCAG[G/T]GGCATGATCATAGCT	80013
rs539372798	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15847212	TGAGAATTCAATTCT[C/T]GGTTTTAACAATTTA	80013
rs539377591	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15821222	ATCATTTTTCAGATG[C/G]AATAGATAAAAGTCA	80013
rs539407319	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15781483	ATAGACACACAAAAA[A/G]GGGAAATCAATGCAG	80013
rs539408987	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15793160	ACCTGAATACGAAGC[A/C]CATATCCAAACATTT	80013
rs539417693	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15814471	AATTCCCCCCACCCC[G/T]AGTGTGCCAGACTAT	80013
rs539460545	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15806636	TGTTTAGCTTTCCAT[A/G]TCAAGACAGACTTTC	80013
rs539465777	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15815440	AACTTAGCATTGTCA[A/T]TTCAGACTAGAGTAT	80013
rs539533555	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15820518	TATATGTGTTAGGGG[G/T]AAGGGGACACACTTT	80013
rs539578222	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15781554	TGAATCACCTATGTG[C/T]TTTGTCAACGGTTAG	80013
rs539639027	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15821519	CTGCTGGTTTAGGGT[G/T]GGGGATAGGAAGGAA	80013
rs539702640	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15792261	CTTCTGGCTCCCCAG[G/T]GGGCAATGAGTTCTG	80013
rs539718686	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15799882	TTAGCTAACTGCGAG[C/T]TTCTCGTGAGCTATT	80013
rs539724336	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15830929	TAGAAGCCACCTAAA[C/T]TTTGTGTAGACCAGG	80013
rs539739167	snp	C/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15837946	TTTGTTTAGGTCACA[C/G]AAACATTAAGCTAAA	80013
rs539837326	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15788102	TTTCTTCTTTCTCTT[C/T]CTTGTCTTAGGCTGG	80013
rs539838722	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15849913	AATTTTCTTACCACA[C/G]AATTTACTTAACCCT	80013
rs539842930	snp	A/G	0.00478085	0.0486577	intron-variant	FAM188A	GRCh38.p7	10:15823889	CCCACATATAAGTAA[A/G]AGCGTGTGATTTTGT	80013
rs539853526	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15845099	TCTCTTAGAGTGTTG[A/T]TGATACATTAAGTTT	80013
rs539870556	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15784167	CTCATTGTCAAAATG[A/G]GGAAGATAATAGTAT	80013
rs539893222	snp	A/G	0.00438332	0.0466095	intron-variant	FAM188A	GRCh38.p7	10:15846391	AGGAATCTTCAAATT[A/G]AGGTAACATTCCTAC	80013
rs539906872	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15855889	AAATATAGTACAAAT[A/G]TAAGATATTATCACA	80013
rs539911365	snp	A/C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15855015	TCTGCTAAACTTTTC[A/C/G]TGTATGAAATTAAAG	80013
rs539953035	snp	C/T	0.00199481	0.0315187	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15861987	AATCTTACCTATCCT[C/T]CATGTCAGAGTGTGC	80013
rs539954999	snp	A/T	0.00119737	0.0244387	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15783609	ACAATTGTCTAAATA[A/T]TTTGAGAAGGAATCA	80013
rs539972358	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15790795	AATGCTCCACGGTGT[A/C]ATATTGGCACTCAAA	80013
rs540070022	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15820197	CGATCTGCAGTCCAG[C/T]CTGAAGGGGACAGTG	80013
rs540143393	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15803459	CTTCAGAGGTATAAC[C/T]GCCGTATTTTTCTTA	80013
rs540228024	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15830345	TTTTTGCCATTTTCT[C/T]ACCTCATTCTAACTA	80013
rs540236107	snp	C/T	6.26586e-05	0.00559691	utr-variant-5-prime, nc-transcript-variant	FAM188A	GRCh38.p7	10:15860336	TCTTCGCTTTGCGGA[C/T]TCCTGCCCCGGAACA	80013
rs540287903	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15858353	CGTTCTAATAAGTCA[C/T]TATAAAGTTCTATTT	80013
rs540336052	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15835744	CACAGCTACTCCGAA[C/T]ATCTACACAACTAAG	80013
rs540374091	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15858831	GTCTTTCACAGTATT[C/T]TAGAGCTGCTTACTA	80013
rs540429309	snp	A/G			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15786336	CGTATCATTATGTGT[A/G]TAGACTGGTGTCTGC	80013
rs540433901	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15797456	TGTATACGCCCAAGT[A/G]ACATGTTTTCATTTG	80013
rs540493227	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15840675	AGCACTTGGGACTAC[C/T]AATTATAAAAAACCA	80013
rs540504620	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15822866	AGTCTTTTCATAAAC[A/G]ATACCCTTCAGCTAA	80013
rs540520525	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15828025	CTATCAAAATTTAAC[A/C]GATGTTCCTCAAGAA	80013
rs540521306	snp	A/G	0.00318978	0.0398085	intron-variant	FAM188A	GRCh38.p7	10:15811830	TACAGAACATATAAA[A/G]CTAGTATTTATAACC	80013
rs540564989	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15788494	TGCTGAACTCTTTCA[C/T]TATGTTTGATAAGCT	80013
rs540640334	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15801744	GGCCATCACTGTTAC[A/C]GAAAAAGCTAATCCA	80013
rs540722519	snp	A/G	0.00119737	0.0244387	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15782824	GAAAGGATATCCTAT[A/G]TATCACTAACAGAGT	80013
rs540723435	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15850971	CTACGTTGAAATATT[A/G]GGTGCTGGTTCCCCC	80013
rs540725899	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15852507	TTAAAAAGTGAGCAG[A/G]GGCTGAGTCAGCAAA	80013
rs540738367	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15850824	CTTGCTGGTTTTGCG[A/G]CTCAGGGGGCATCAT	80013
rs540740943	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15823286	TTAGGATTCCTCAGG[A/G]ACCACAAGACCCTCT	80013
rs540751783	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15808688	TCTGTCATGGATATT[C/T]ACGTGTTCATGCCTG	80013
rs540828092	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15804442	TGGGTTGGCTGGGGA[C/T]AAGTAATTCATTACT	80013
rs540877173	snp	A/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15816126	ATTAGCTGGGTGTGG[A/T]GGCATGCACCTGTAG	80013
rs540961268	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15788630	ATCCACTTAAGAAGA[A/G]TTATTTTTTCATGGA	80013
rs540969147	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15808788	AACCATAAAAGAGAA[C/G]AAAAAAGTGATGTAA	80013
rs541035236	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15795324	TCTTAGAATTTGCAT[A/G]ACATGGATTTTCAGA	80013
rs541046543	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15786857	TAATCTGTTACTATT[G/T]AAAATTTAAATTGTG	80013
rs541064438	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15832443	CAAGAGACACTGAAA[A/T]GAGATTTTTTTTTTC	80013
rs541099592	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15827292	CACGCCTGTAATCTC[A/G]GCACTTTGGAAGGCC	80013
rs541148914	snp	A/G			downstream-variant-500B	FAM188A	GRCh38.p7	10:15777774	CACAGGAACTATACT[A/G]TTGAAGGTAATGTTC	80013
rs541159333	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15786392	AAGGCACTGCGTTAC[C/T]GTATTCGAACACACA	80013
rs541203204	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15850538	GTCTTATACAGTTGT[A/G]GATAAGGGACGAAAT	80013
rs541260448	in-del	-/TACTT	0.00398564	0.0444627	intron-variant	FAM188A	GRCh38.p7	10:15789769	TCAGTGATCCACTGA[-/TACTT]TACTTAGACAACTGA	80013
rs541269274	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15807938	AGATTTCTGGTCAAA[A/G]TAATTAAAAATGAAA	80013
rs541292677	in-del	-/TTATC	0.00159617	0.0282053	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15785722	TCTTTCTTAACAATT[-/TTATC]TTGAGTTTAACAATC	80013
rs541383586	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15856881	CACTACCACTACTCT[G/T]GTCCAAGATAGCATC	80013
rs541460942	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15862283	TTATCTCTCAGCAAG[G/T]GAGAGATCGGGGAAG	80013
rs541504134	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15838154	AAAACTAAGAACCTT[C/T]CCACAGTATGAACAG	80013
rs541514758	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15860914	AGCTGGAGGCTGTCC[A/G]CCTCTGTACTTCAAT	80013
rs541551767	snp	A/C			utr-variant-3-prime, nc-transcript-variant	FAM188A	GRCh38.p7	10:15778521	GTGTTATTTGTCAAT[A/C]TTTCTAATGAAAAAC	80013
rs541551988	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15861481	TTCATATATTGTAAG[G/T]AATAAATGGAAAAAG	80013
rs541618558	snp	A/C/G	3.38634e-05	0.0041147	intron-variant	FAM188A	GRCh38.p7	10:15837340	GAAAAAAAGAATTAA[A/C/G]TATTGGTATCATGAT	80013
rs541645487	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15814820	AGGAAGAGTGTACTC[A/C]TAAAAAGAAGGGCCT	80013
rs541687350	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15835996	CAAAAAGATCTTGTC[A/T]CTCCCTTGTTCAAAC	80013
rs541710947	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15856649	GGCTGCTTTTGCTGC[A/T]ATACCATTAATGAGC	80013
rs541711131	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15816248	CCTGGGCAACACAGT[C/G]AGACTCCATCTCAAA	80013
rs541766790	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15830481	CAGTAGTCTAATTCC[A/G]CACAGCTAACATACT	80013
rs541800193	snp	A/T	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15842894	TCTTGCCCACAGCTA[A/T]ATAAGACTACAAAAA	80013
rs541862644	snp	G/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15805258	TCATAATGATGAAAG[G/T]CTTAAAGAATAAACT	80013
rs541902761	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	FAM188A	GRCh38.p7	10:15778338	AAAGTGTATTTGGCA[A/G]TTACACAGTAAAAGT	80013
rs541913995	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15848135	CCACTCCCAAATGCA[C/T]GTAAGAGTACATATA	80013
rs541979955	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15818388	CTCATGAAATGTTTT[A/G]TAATAGTAAAAATAT	80013
rs542004915	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15830914	TTTTGTTTTAGGCAG[C/T]AGAAGCCACCTAAAT	80013
rs542025505	snp	G/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15784858	CTACAGGGGAAAGGG[G/T]ACATCAGTGGTATGT	80013
rs542043571	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15825526	TAACTGATTATCTTA[C/T]ATAAAAGAGAATGAA	80013
rs542065852	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15818943	TGAATATATTAAAAA[A/G]CCCTGAATTGTATGC	80013
rs542075380	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15853085	CCACTACCCCTCGAA[C/T]ACCAACAGACAACTA	80013
rs542101661	snp	C/T	0.00716266	0.059414	intron-variant	FAM188A	GRCh38.p7	10:15831643	GAAGTAACGACTTCA[C/T]GTCAAGAGCTGCCTA	80013
rs542104033	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15812098	AGGTGCCCAGCACCA[C/T]GCCTGGGTAATTTTT	80013
rs542136461	snp	C/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15798605	GCCAACATGGTGAAA[C/G]CCCATCTCTACTACA	80013
rs542138879	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15823748	TTGAATTTACTCCAT[A/G]TTACAGTATGTTTGT	80013
rs542140155	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15790871	ACCGTTTTTCAGGAG[C/G]ACTGACAGCATGTAC	80013
rs542164915	snp	A/C/T	0.00398564	0.0444627	intron-variant	FAM188A	GRCh38.p7	10:15851106	CTGACCACAAACCTG[A/C/T]GAAACTTTTGTCCCT	80013
rs542200080	in-del	-/C	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15845794	TACAGGTGTGAGCCA[-/C]CCGTGCCTGGCCTAT	80013
rs542206513	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15859785	GGACTTTCCCTTGGA[C/T]GTCCCTCCTTCTCAC	80013
rs542207625	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15785083	AACCTGAGAATTAGC[A/G]TTTCTAACAAGCTCT	80013
rs542252235	snp	A/G	0	0	intron-variant	FAM188A	GRCh38.p7	10:15798165	GCTGGTAATTTCTAA[A/G]TATTATTTAAAACTA	80013
rs542255663	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15829371	AAAAATATATGAATG[C/T]CCAGATTCCAGCTGA	80013
rs542266736	snp	C/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	FAM188A	GRCh38.p7	10:15782419	AGTGTTGCCTCTGAA[C/G]AAGATGCTGGAAAGT	80013
rs542290607	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15783096	AAGGGAAGACAGCTG[C/T]TGGCAACTGGAGCTT	80013
rs542306194	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15830936	CACCTAAATTTTGTG[A/T]AGACCAGGGAAGAGA	80013
rs542307897	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15789787	CTTAGACAACTGACA[A/G]ATTAACAGCAAAGGT	80013
rs542308013	snp	C/T	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15796645	AATGAGATAGCAATG[C/T]ATTAAAAATTTTAAT	80013
rs542332647	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15787914	TATTACAGTTGTAAA[C/T]AGGCCAAAGTAGAGT	80013
rs542368286	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15834351	GCCCCAATAAATGCA[A/T]ACATAAAATGAAATT	80013
rs542418400	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15796012	CATTAAATAATCCAA[G/T]ATATCTTTTGAATAA	80013
rs542454749	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15860156	CACAGGCGGACTCTC[A/G]CAGGGCAAAAGAAGC	80013
rs542509066	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15851595	TCAAGGCTTCAAAAC[G/T]TATCTTTAACGTGTC	80013
rs542644277	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15829867	CACAGGTAAGAAAAC[C/T]GAGGCTCAGATAATT	80013
rs542666973	snp	A/G	0.00199481	0.0315187	intron-variant	FAM188A	GRCh38.p7	10:15846915	TTTTTAGTAGAGACG[A/G]GGTTTCACCATGTTA	80013
rs542667777	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15801185	TATTCCGGCATGGGG[A/G]GGAAATGCCATAAAG	80013
rs542783951	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15803292	TAACTTAAACACTTG[C/T]AAACAGGGTTCCTAG	80013
rs542811554	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15803339	CTAATCCATGTAGCA[A/G]ACTTAATATTAATAT	80013
rs542821150	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15840835	AAACCACAGAATATA[C/T]AATTTTTATGAATAA	80013
rs542852915	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15832968	TCAGAGAGGCACACT[A/G]TGGTTACTTAATGTA	80013
rs542867591	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15787906	CCATTCTGTATTACA[A/G]TTGTAAATAGGCCAA	80013
rs542906269	in-del	-/TT	0.354665	0.227036	intron-variant	FAM188A	GRCh38.p7	10:15798464	TCTAAGTGCCAAGTG[-/TT]TTTTTTTTTTTTTTT	80013
rs542968903	snp	C/T	0.00597247	0.0543191	intron-variant	FAM188A	GRCh38.p7	10:15816201	AGGAGACGTAGGTTG[C/T]AGTGAGGCGAGACTG	80013
rs542982612	snp	A/G	0.00318978	0.0398085	intron-variant	FAM188A	GRCh38.p7	10:15846966	CTGACCATGTGATCC[A/G]CCCACCTTGGCCTCC	80013
rs542989206	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15845881	GAGCTAGAGTGCAGT[A/G]GCGTGATCTCGGCTC	80013
rs543064744	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15850119	TGAACATAAACTGTG[A/C]AGATTTCATGGACAT	80013
rs543116495	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	FAM188A	GRCh38.p7	10:15782323	TTTCTCAAATCCTTA[C/T]CCTTTGACTGGGGAC	80013
rs543120574	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15828682	AGACGTATATACAAA[A/G]CATGTTTACTACAGC	80013
rs543138728	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15857753	GAATTATCTAAAAAT[A/G]TCAAGCCAATTAAAA	80013
rs543147539	in-del	-/ATG	0.00318978	0.0398085	intron-variant, cds-indel	FAM188A	GRCh38.p7	10:15785920	TCTGATAAAATGACC[-/ATG]ATATCTGTTATCTAG	80013
rs543155011	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15849076	AGATAATTACTAAAA[C/T]AAAGGAATAAACTAA	80013
rs543250760	snp	A/T	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15821378	TAAATTCATATTCAA[A/T]AATAGATGTCTGTGG	80013
rs543259666	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15842703	TTGTAAACTGTCACG[C/T]GGAATGCAAATTCTT	80013
rs543270407	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15839258	GAGTGTTTCATATTT[C/T]GTTTTAAAATCTTTA	80013
rs543273553	snp	C/T			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15784203	TTGGAAGGCACACAG[C/T]GCCTGATGGAGAGTA	80013
rs543279945	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15828123	AAATATACATCTCAT[A/G]AAAACTTGTACATGA	80013
rs543304855	snp	C/T	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15786351	ATAGACTGGTGTCTG[C/T]GTCATCTTCTGCTGC	80013
rs543317966	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15832523	AATAGGATGATCTCA[A/G]TTAAAGAGAGCTGAG	80013
rs543325800	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15826763	TAAATATGGAAAAAT[A/G]TGTTCAACAAAAAAC	80013
rs543334851	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15794294	CATCCTGAAACAAAA[A/G]CATATCATTTGGGGA	80013
rs543335246	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15801524	CCACCCAGAATCCCA[A/T]GAGCTCACCACCAAA	80013
rs543372013	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15850628	AAATTTTAGTCAGAC[C/T]GGTTGTCTGCTCTCA	80013
rs543398850	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15801307	ACCAGGACTGCCCTT[A/G]TTTATAAAACTGCTA	80013
rs543448845	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15801042	TGGCTTTAAAAATAT[C/T]AAGGTAACAGGAGAA	80013
rs543451928	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15838126	TTTATGTTTAAGTAG[C/T]GCATTTCTATGTAAA	80013
rs543468321	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15793247	GTGGAACACTTTGAA[G/T]AGACCTGATAACTGC	80013
rs543483756	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15807226	TATTATTAATCCTTA[C/T]GTTCCAACAGTACTT	80013
rs543512801	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15799999	CAAAGAACTAAGAAG[A/C]GAGTACAGTTGATCC	80013
rs543513522	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15803808	AAGTTCTAACAAATG[C/T]ACACTAATCCTACAC	80013
rs543610005	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15806087	TCGCCCCCTTCTTGA[A/G]TACCACTGTGTACAG	80013
rs543614118	snp	C/T	0.00279162	0.0372561	intron-variant	FAM188A	GRCh38.p7	10:15798728	GAGGTTGCAGTGAAC[C/T]AAGATCATGCCATTG	80013
rs543616801	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15856004	ACGAATTAAGAAATA[C/T]TGGTTGTTAGGCAAA	80013
rs543650574	snp	C/T	0.00199481	0.0315187	downstream-variant-500B	FAM188A	GRCh38.p7	10:15777980	TCTAGAAAGCTGCCA[C/T]GTGGGTTCTCATGCT	80013
rs543685690	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15803763	AAGAATCTTATTAAA[C/T]TTATCCTAAGAAAAT	80013
rs543729563	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15862193	AATTCTAGCATGGGG[C/T]CTTGAACATCACTGG	80013
rs543750995	snp	G/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15779904	AAACATACTTAAAAA[G/T]TATTTTGGACATATC	80013
rs543788590	snp	C/T	0.00318978	0.0398085	intron-variant	FAM188A	GRCh38.p7	10:15831678	GCCTCCTTTTCTTTT[C/T]TTTTTTTTTTTTTTT	80013
rs543812137	snp	G/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15819088	AGAGGGAGAGTGCAG[G/T]AGGGAGAAAGAGATT	80013
rs543814799	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15785597	GAAGGGTCTAATGTC[A/G]GACAATAAAATCTAA	80013
rs543843533	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15853144	AATGATAGTTTGAAG[C/G]GTAGTTGGATCAAGA	80013
rs543902378	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15845254	CCACTGATCTTAGTT[C/T]CTTCTTTATTCCTGG	80013
rs543922981	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15852739	GTTGAAGTGTAATTC[A/G]GATTAGAAAGAGAAA	80013
rs543941119	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15815607	ACGAACATTCAGCAA[C/T]CTATCAAGTTACCTA	80013
rs544047748	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15854362	TATATTGCCACAGAC[A/T]GGAGAAGCCAGTGTA	80013
rs544096804	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15850206	AATCCCGTCATCTTC[A/G]TAAGCTGAGCATGTA	80013
rs544180151	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15825399	TTTATTATCAGAGAC[A/G]GTGTCTTGCCTTCTT	80013
rs544184956	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15848052	ATCACAACAGCAAAA[C/T]ATCTTCAAATCATGA	80013
rs544190071	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15835184	AAGTGCCTTCTTTTC[C/T]TAAAAACCAATTTCC	80013
rs544207198	snp	C/T	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15790281	CTTAAACCTCTTTTC[C/T]ATTCTTAAACCTCAT	80013
rs544211855	snp	A/G	0.00159617	0.0282053	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15860813	TGCTTGTATTTTTCA[A/G]TATTAATTTTGCAAA	80013
rs544241460	in-del	-/T			intron-variant	FAM188A	GRCh38.p7	10:15849446	ATATCATCTTACTGG[-/T]TTTTTTTTTTTTTTC	80013
rs544277922	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15835293	ATTGTAACCTCATCA[A/G]TTCCAGAAGGACAAA	80013
rs544294144	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15784233	ATGTGCTTGGGAAAG[C/G]GGAGCTGCTTCTGCT	80013
rs544348228	snp	C/T	0.00597247	0.0543191	intron-variant	FAM188A	GRCh38.p7	10:15852891	CATGTACAGACTTTC[C/T]TTTTCATATCATTCC	80013
rs544446823	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15823692	TGCTCAAGTACAATG[C/T]AATTTTCTTAAGCAT	80013
rs544500706	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15859024	GGAATCGAGAGACCT[A/G]GAATCCACTCCCAGT	80013
rs544507942	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15797667	GAAAGGTTTATTTAA[C/T]CTGAACAGTATTTCT	80013
rs544519976	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15830840	TGCGGGCAAGGAAAT[C/T]CTGCTGGTGAAAGGA	80013
rs544522915	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15817692	TTAACTTAAAAATGA[C/T]GAATCTTAGCAATAC	80013
rs544652380	snp	A/T	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15859564	TAAGTAAAAGTCCTG[A/T]CTGGGTTACAAGCAT	80013
rs544672880	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15818319	ATTAAGGTAGAAGTA[A/G]AAAAAAAAAACAAAC	80013
rs544706583	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15819578	CCACAGGGGAGCTCA[A/G]GCAATCTAGCTGACC	80013
rs544768975	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15808891	TGAAACTAGATGCTA[C/T]AGGCAGGGTCCAACT	80013
rs544806614	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15809809	TCCTTAGGATACTAT[A/G]TCAAGGAGTACAATA	80013
rs544809489	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15794112	AGATATAAAAATACT[C/T]CTGGGTACCTTCAGT	80013
rs544820382	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15794651	CAATTCTGAAAAATT[A/G]CACTGATTATAAATT	80013
rs544921036	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	FAM188A	GRCh38.p7	10:15782425	GCCTCTGAAGAAGAT[A/G]CTGGAAAGTAGGGAA	80013
rs545003736	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15796523	AAAACAAAACCCAAA[C/G]CATTTTTTCCACATT	80013
rs545017511	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15834301	AATGGATTTGTTAAA[A/G]TACCTCCCCACTGTT	80013
rs545026507	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15781917	GGGTAACGATCTGTA[C/T]GGGGGTGTATTTAGT	80013
rs545066855	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15799720	ACTGAGAACTGTGAC[A/G]GAAAAGGAGGACTTA	80013
rs545097603	snp	A/T	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15787057	TAAAATACAGGGTCA[A/T]AAGGCAGTGGTACAT	80013
rs545112950	snp	C/T	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15822033	AATCCATGCCATTGT[C/T]GACAAAAATACAAGA	80013
rs545172627	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15846470	TAATTTGTAGTTAAA[C/T]CTCATTCTTCACATT	80013
rs545245494	snp	A/C	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15800953	TACAAGCTAAAGCAA[A/C]ACAAAAGTAAAGGAG	80013
rs545267011	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15850454	AATTCTTTTTCTCAG[C/T]AAGGAACAGCCCTGA	80013
rs545290338	snp	C/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15832292	AAGTTCAGCAAGAAC[C/G]TATTGCTTCCCTAAT	80013
rs545370497	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15850987	GGTGCTGGTTCCCCC[A/G]ATAAGTGAACCAAAC	80013
rs545376080	snp	C/T	0.00199481	0.0315187	intron-variant	FAM188A	GRCh38.p7	10:15850070	CCAAATTAATACTTT[C/T]ATAATTTCTTACGCC	80013
rs545385671	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15845791	GGCTTACAGGTGTGA[A/G]CCACCGTGCCTGGCC	80013
rs545454744	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15855387	CAGGACACAGCATTA[C/T]TTTTCTTCTCAAGAG	80013
rs545460756	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15859983	GCCCGGAGGATGGAA[A/G]GAGCGCTGCGGGTAT	80013
rs545535779	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15832837	AATTCAAATGGAAGA[C/T]CATGAATCACTTCAA	80013
rs545537016	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15862140	TTTGCTTTTCTCTTG[G/T]GATATAAATTTATGG	80013
rs545605915	in-del	-/A	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15797596	AACATGTAACATCAT[-/A]AAACGTGCAGTTATA	80013
rs545669286	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15800335	GTCAAGAGATGTAAA[C/T]GAATGTAAAGATGCA	80013
rs545693684	snp	A/C	1.67161e-05	0.00289098	intron-variant, missense, utr-variant-5-prime, nc-transcript-variant	FAM188A	GRCh38.p7	10:15838274	GCTCTTCGACAGCCA[A/C]GGCAGCTATACATAA	80013
rs545700310	snp	C/T			downstream-variant-500B	FAM188A	GRCh38.p7	10:15778043	TAGCATAAGGCCTGG[C/T]CTCTTATTCGAGGTC	80013
rs545717998	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15848409	GGAGGCAGAGGCGGG[C/T]GGATCACGAGGTCAG	80013
rs545722699	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15826619	ATGTAGAAAAGACTA[C/T]GACAATTTTGTAAAA	80013
rs545776086	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15792559	AGGAACAGAAAAGAC[A/C]AGGCAATTCTAGAGA	80013
rs545788596	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15836545	ATTTCAGACATGATA[A/G]ATCTAATAGCATAGT	80013
rs545823998	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15831010	TCTGGAAAGATATAT[A/G]GTTCTTCTAAAACAG	80013
rs545890300	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15799241	ATCTTGCTCTGTTGC[C/T]CAGGCTGGAGTGCAG	80013
rs545913211	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15803476	CCGTATTTTTCTTAT[C/T]GTACATAAAATGGTT	80013
rs545949550	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15812796	AGTTACATTCAACAA[C/T]AGCAAAGCTGCTAAG	80013
rs545955077	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15802278	TTCACACTGCTATAA[A/G]GATACTACCTGAGGT	80013
rs546007375	in-del	-/TC	0.00279162	0.0372561	intron-variant	FAM188A	GRCh38.p7	10:15815014	TTTAAAATATTGTCA[-/TC]TTTTATATTCAACAC	80013
rs546020453	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15820322	TGGCTGGAGCACAGC[A/G]GTAGAGAAAGCAACG	80013
rs546033141	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15813156	TACTCCCACTACCAA[C/T]TTTTAACAAGTCTAG	80013
rs546036979	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15804895	TATTTTCCAAATAAC[A/G]TGTAAAGCCCAGGTC	80013
rs546039778	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15819420	TTCCCTTGCAAAAGA[C/T]AGCTAATTAAGTTCT	80013
rs546060694	snp	C/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15830157	ACCAATGTCTGCCCT[C/G]AAGTGTTTCAATTTT	80013
rs546062298	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15848566	GTGAACCTAGCAGGC[A/G]GAGCTTGCACTGAGC	80013
rs546141973	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15818037	AAGGAACAAAGAAAG[A/G]GGGAAAGATAAAATC	80013
rs546153837	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15785551	TAATCCAGATATCCA[A/G]TCAGAATGTGAACAA	80013
rs546158987	snp	A/G			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15785432	AGGAATATTCTTTTT[A/G]TTATAACTAAGAATC	80013
rs546189756	snp	A/G	0.00279162	0.0372561	intron-variant	FAM188A	GRCh38.p7	10:15791784	CATGTAATTTCCTGG[A/G]TAAGATAACTATTTC	80013
rs546242863	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15783125	TTCAGCTCCTACAGA[A/G]AGATAGGCTGTGAGA	80013
rs546274012	snp	A/G			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15782863	AGAAAAATGGGTCAT[A/G]TTATTCCCACTATCT	80013
rs546287558	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15843707	GTGACACAAGATTAA[C/T]ACTATTAGAGTCATC	80013
rs546311842	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15818442	TCACTTTGGACAACA[A/G]TTTGACACTTCCTCA	80013
rs546337204	snp	C/G			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15779822	GTATATGCAGTGGCA[C/G]TGATCACAGAAATAT	80013
rs546337273	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15825128	GAAAATCTGAAATCC[A/G]AAATGTTCCAAGATC	80013
rs546401265	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15854073	TCCAAATCACTGATG[C/T]ATACTGTTATAAATT	80013
rs546471079	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15829028	AAATGCCTACACTGG[C/T]CCACAGAAAAAATTC	80013
rs546496210	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15819049	AGCCACCTTATTCTT[C/T]GTTGGGTTTGTACGT	80013
rs546568598	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15860769	GAGGCTCTGAGGCCC[A/G]GGCACTAGGAATTAG	80013
rs546644022	snp	A/C	0.00279162	0.0372561	intron-variant	FAM188A	GRCh38.p7	10:15852608	AGCAAAGAGTAGTCA[A/C]CTATTACAAATGCTG	80013
rs546644104	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15859825	ACCAACCACCACCAA[C/T]AGACAGCTCTGTTAG	80013
rs546726776	snp	A/C	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15795535	AGTGAGTTAGCTATA[A/C]TAAAGTCTTAACCGT	80013
rs546749930	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15859262	GGTTTATATTTACTA[C/T]GCCAAAATTCCGCCC	80013
rs546809542	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15834461	GACAAACAAAATTAC[A/T]TGACTCAGTCATGTT	80013
rs546857023	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15796261	GGCAGACATAATGAC[A/G]TTGGAGTCAGAAGAC	80013
rs546883065	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15833295	CTTTGTAATGCTCCA[C/T]TTTAAGCAAAGAGTG	80013
rs546886842	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15840974	AATATCCAAATAATT[C/T]GGAAAGAAAAGAAAC	80013
rs546921093	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15857225	TTTCTGTGAAGTTTT[C/T]TATAACTACCATTTG	80013
rs546921610	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15833796	ATAAAGTAATGACTT[C/T]TCACATTAAATTATG	80013
rs546931091	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15781366	GAATGTTAGACCTTA[C/T]TCCTTTAATATTAGC	80013
rs546947355	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15827538	ACAGAGTGAGACTCC[A/G]TCTCAATAAATAAAT	80013
rs546954778	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15847012	ACAGGTGCGAGCCAC[C/T]GTGCCTGGCCAGAAT	80013
rs547058627	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15838577	GATAATCAGTGCCTC[A/G]CATATCATAATGTGT	80013
rs547087505	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15830029	AGAATGGAGAATCTC[A/G]AAGACTCAGCAACTC	80013
rs547101512	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15853360	ACATGATAAAACTAA[A/G]ATATGATTTGCCCCT	80013
rs547133005	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15839303	TTAAGTTATTTCTTG[A/G]TTTATGTGGGAAACA	80013
rs547138465	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15809368	ATTCAAAAAGTTTAA[A/G]TTCTGTATTCCTTAA	80013
rs547154971	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15851606	AAACGTATCTTTAAC[A/G]TGTCCATTTCCATCC	80013
rs547168466	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15822267	AAGAATAGAAAATGA[A/T]CTCTGCCTTAGAAAG	80013
rs547191262	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15850708	AACATGAAACTTCAT[C/T]AGCAATTCTAATTTT	80013
rs547248641	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15816376	ATATTAAAATTGTGG[A/G]AAGTATTCCATCTTA	80013
rs547277956	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15828229	TTTGTGCAATGGTAT[C/G]TTATTCATCAATAAA	80013
rs547288282	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	FAM188A	GRCh38.p7	10:15782008	GGTCAAATCCAAAGA[C/T]GGCTGATTCTAAAAT	80013
rs547308431	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15814994	ATCAATTATAAAATT[G/T]AAGATTTAAAATATT	80013
rs547381177	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15820492	TTCTTTAGGATCTAC[A/G]AATGTGTGTGTATAT	80013
rs547388092	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15794416	CACATAGCTAAACCA[C/T]GAACAGTGTGATATT	80013
rs547388496	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15786508	TGCTGCAAACAATCA[C/T]AGGTAATCATCCCAA	80013
rs547424544	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15845948	CTGCATCAGTTTCCC[A/G]AGTAGCTGGGATTAC	80013
rs547467091	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15781090	GATGAAGCACTCATT[C/T]GCACATTAGAAAACA	80013
rs547479246	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15813224	GCTATTCTTCCAGCT[A/T]CATCTTACACCTTGT	80013
rs547480861	snp	A/C	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15785653	AGTTTTAAGAAGTCC[A/C]GTAGTCTACATTGTC	80013
rs547502015	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15793825	AGTGCTTCAGAAATC[A/G]TAACATTCCACGCAA	80013
rs547532126	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15799817	GGTTAAACATCCAAG[C/T]AGAATACATGGAGTT	80013
rs547594022	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15785160	GGATCACATGCTCGT[A/G]GGAGGCAAACAGCAT	80013
rs547594112	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15792763	TAATTGTACAAGGGG[A/G]AGGGGATAAAGGAGA	80013
rs547714207	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15844939	AGCATCATTCCACCT[A/G]TTATGACTGCACATC	80013
rs547750858	in-del	-/AAGA	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15812654	GGAGGGAAATACAAG[-/AAGA]AAGTCATGTCAGAGA	80013
rs547784774	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15801182	TCCTATTCCGGCATG[C/G]GGGGGAAATGCCATA	80013
rs547812527	in-del	-/TCTTTTCTATTCTTAAACC	0.0123036	0.0774623	intron-variant	FAM188A	GRCh38.p7	10:15790255	ATGATTGTAGAAAGG[-/TCTTTTCTATTCTTAAACC]TCTTTTCTATTCTTA	80013
rs547839304	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15825810	CCATCATCTTTCAAT[C/T]AGCTATGCATTTGAC	80013
rs547922615	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15805633	ACTTTTCTCTGAAAT[A/G]GGCCTACTTCCTTGC	80013
rs547989620	snp	C/T			utr-variant-5-prime, synonymous-codon, nc-transcript-variant	FAM188A	GRCh38.p7	10:15837318	TCTGAACGATCTTTT[C/T]CTGGGGGAAAAAAAG	80013
rs547999809	snp	G/T	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15850381	TGACTGTCTGGGAGC[G/T]GGGCAGAACAGAGTC	80013
rs547999860	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15807125	GTTTGAGGATTAAAT[A/G]AGGAATGCTCCTGAG	80013
rs548066680	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15843953	CACCTATTCTCTCTG[A/C]ATCTCTAGAGGGCAG	80013
rs548081462	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15841903	ACTTTCTTAAAACTT[G/T]AGCAACTGCAGCATT	80013
rs548106326	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15853279	GAGACTTTTAAAGGT[A/G]GTCCACCGATAACCC	80013
rs548113796	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15860008	GGGTATTTAGTGGCA[C/G]CTGTAACCATTCTCC	80013
rs548125694	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15805063	CGCAGTGGGAGAAGA[A/T]GTTTCCAACAGATGT	80013
rs548137256	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15810759	TCACAGAGCTTACTA[C/G]AGAGAGAGACAGATA	80013
rs548191072	snp	C/G/T			intron-variant	FAM188A	GRCh38.p7	10:15792997	ACTGAGGTAGGAACT[C/G/T]GTCCAACATCACACA	80013
rs548251856	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15808402	AGCACCACTTTACAG[A/C]TTTTCCTTAACACCG	80013
rs548276459	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15811918	TTGCAATAATGCTTA[A/G]TTTTTCATTTTTTAA	80013
rs548315914	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15842325	GAACTATGCTGTTCA[C/T]TTTCTAATCACCACA	80013
rs548330070	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15812933	TACCTCAGGAGTAAA[A/T]CTCTGAAATCCATGC	80013
rs548357611	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15859608	GTACTATGATCCATA[C/T]TCCTTTTTTAACCGT	80013
rs548399658	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15818756	CTATATACTACATGA[C/T]TCCATTGGTATGAAA	80013
rs548402385	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15828850	CTCTGACAACATAGT[A/G]GGAGGCAGGCAATAT	80013
rs548420525	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15783788	TAATTACAGGAGTCA[C/T]TGCAATTAGTTACAT	80013
rs548436867	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15830041	CTCGAAGACTCAGCA[A/G]CTCATTAGATACATG	80013
rs548439353	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15834765	TGAAATGGGGGTGCA[C/T]TTGAGATAACTTTAA	80013
rs548442222	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15819147	TGTATAATCAAAATG[A/T]TATTGCAAAATGTTA	80013
rs548445702	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15838127	TTATGTTTAAGTAGC[A/G]CATTTCTATGTAAAA	80013
rs548450159	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15803050	ATAGTCTTCTAAAGT[A/G]ATTACTGGCTTGCTT	80013
rs548464323	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15859349	TACATACATAAATTA[C/T]TGATCCTTCTGACTC	80013
rs548495615	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15817856	GTGGAATTTATTCTT[A/G]TCACTAGGAGGGAAG	80013
rs548501802	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15847175	ACTGTCATTCACAGA[C/T]ATCATCAGTATTACA	80013
rs548542698	in-del	-/ACTT	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15798927	GAAAGAGCATTTGGA[-/ACTT]ACTTAGGCAAAAATC	80013
rs548568357	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15822997	TTTTGCATCCTTTTT[A/C]CCATCTGGTCATGTT	80013
rs548572733	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15789727	AAATTCCCTTTGTCA[C/G]AATGTTATTTAGTTT	80013
rs548604605	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15817157	CAATATAGATTTAAC[A/C]CAGCTGGAGATAACT	80013
rs548609390	snp	C/T	0.0023933	0.0345097	intron-variant	FAM188A	GRCh38.p7	10:15790331	TGAAGACAGATTGGC[C/T]TTGACTAAAAGGTTA	80013
rs548636110	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15795060	ACACAACACAACACA[C/T]AACGATTACATGAAA	80013
rs548679577	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15822416	GATAACAGGGAGTTG[A/G]ATCTTGAAGCGTATT	80013
rs548706401	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15858508	TGAGTGTTCACTATA[A/C]GTCAGATAGTGTGCT	80013
rs548721437	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15811330	TATTTAATCGCTGAG[A/G]CCTTAGTTCATCCTG	80013
rs548733848	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15826022	AATGTACAAATACTG[A/G]AGAATTCCTTTAAGA	80013
rs548738149	snp	A/T	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15795456	AACTTCCATTTCTAC[A/T]CGGTACTTCGTAAGG	80013
rs548759483	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	FAM188A	GRCh38.p7	10:15782087	TACGGGAATCGAACA[C/T]TGTTACATACTCACA	80013
rs548846559	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15857265	GAGCACTCTTTCTTC[C/T]GACTTCTGCATGACT	80013
rs548890047	snp	G/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15833168	AATGGAAGTGGTAGT[G/T]GAAGAGTTGGTAATT	80013
rs548893474	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15852516	GAGCAGAGGCTGAGT[C/G]AGCAAAGGAGACTGA	80013
rs548976927	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15802400	GGAGAAGCAAGCACC[C/T]TCTTCACAAGGCAGC	80013
rs549011700	snp	G/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15801286	GCACATGCAGTCAGG[G/T]TGATGACCAGGACTG	80013
rs549055788	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15788780	AATATATTGCAGCCA[C/T]CCCTAAAAGTTTCAG	80013
rs549067237	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15808277	GAGGCACGAAATCTC[A/G]ATATATGCACAAACT	80013
rs549073824	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15828957	TTCCTTCTTCATAAC[A/G]TATGGAGTAATACTT	80013
rs549115899	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15805407	AACAGAGAATAGTTA[C/T]ACTGGTAATACAGAT	80013
rs549130149	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15862417	GCTCATAACTGGCAG[A/T]CTTCTAAGTTCAGAA	80013
rs549202308	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15857057	CCCCTATTTCATGTA[C/T]AAGATGAGTGAAAGT	80013
rs549209326	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15832591	GTTTAAACTCTGACC[C/T]TTACTAGAAATCACC	80013
rs549240951	snp	C/T	0.00199481	0.0315187	intron-variant	FAM188A	GRCh38.p7	10:15850682	TATCAATGACAATGC[C/T]GGCCCAGTACAACAT	80013
rs549254238	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15846586	AAAATAAATGATCTA[A/T]AAAAGATATTTTGGA	80013
rs549327699	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15851382	TTATCTGGCTCCTGC[C/T]TGCATCTCCCTCTTC	80013
rs549338487	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15840169	AAAATTTTAATATCC[C/T]AAATGAACCTATTAA	80013
rs549344595	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15792279	GCAATGAGTTCTGGA[A/G]GGCAGGGAGTCCAGA	80013
rs549372835	in-del	-/C	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15849993	CCCTGAATGGAGGGA[-/C]CTGCTGAAGCTGTGA	80013
rs549376462	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15851038	CAGTCATCAGTACAG[A/G]CTAGTTCCCAAATCT	80013
rs549404574	snp	A/T	0.000399281	0.0141238	intron-variant, synonymous-codon	FAM188A	GRCh38.p7	10:15786457	GTTTTCTCAGTCTCA[A/T]ATCTGCGCATTAGGA	80013
rs549417909	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15844902	CCTAGTGAGGGTGAG[A/C]ATCCTGATTATTTGG	80013
rs549432632	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15780333	TTTATTTTAGTTAAT[A/G]TATTAGTTTCTAGTG	80013
rs549505836	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15845409	GTTTTAATATATGTA[C/T]TTGCTCACTTCTGGT	80013
rs549514037	in-del	-/ATTT	0.00438332	0.0466095	intron-variant	FAM188A	GRCh38.p7	10:15796606	AAATAAAATCCAGAG[-/ATTT]ATTATAGCAAATAAT	80013
rs549587051	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15781258	TCTTTTAGATTTGGT[C/G]TAATTAAAATTATGT	80013
rs549596676	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15821096	TCAGATTGTGTAGGA[A/G]GAGAATGAAATAAAC	80013
rs549663547	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15814361	TACACAATGAAGCAT[C/G]ACAATGAGTCGTGTA	80013
rs549679345	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15820392	AAATATTTCCAAATA[C/T]AAAATCTCCACCCCC	80013
rs549681937	snp	C/T	9.90344e-05	0.00703615	utr-variant-5-prime, missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15843220	ATCATACCTGAACAA[C/T]CCCGCCAAGAAGACT	80013
rs549709018	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15827031	AGACTGAGGCAAGAG[A/G]ACCACTGGAGCCCAT	80013
rs549736299	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15831866	TTTCTAGTAGAGACG[A/G]GGTTTCACTGTGTTG	80013
rs549750268	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15806316	GGAGGAATCTCCACA[C/T]ACGCAGACTTCATGT	80013
rs549771679	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15793028	GCTAGTGAGGCGTAA[C/T]GGATGGAGCCATTTT	80013
rs549801016	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15861711	TTGTAGAATACCCTT[G/T]CATTTGGCTAATTAA	80013
rs549831988	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15855460	TTACCATAAATGGCC[A/G]TTTTTCCTGATTACG	80013
rs549874328	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15825103	GTCTATTTTCAAGTA[G/T]TCCTAATCTGAAAAT	80013
rs549881826	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15799640	CTAGCTAGAAGGAAC[A/G]GAATCAGGAAAGGCA	80013
rs549887586	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15837730	TAACTTACACATTTG[C/T]GGCTTCTTTTAAAAG	80013
rs549896414	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15808895	ACTAGATGCTATAGG[C/T]AGGGTCCAACTATTT	80013
rs549929630	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15800736	GTGGTTGCTCACTAT[G/T]TCAAGATAAATGAAT	80013
rs549949063	in-del	-/TGAC	0.00677013	0.0577861	intron-variant	FAM188A	GRCh38.p7	10:15848745	TTACCCAACCAGCAT[-/TGAC]TGATAGCAGCTAGCG	80013
rs549956855	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15796588	CAGTTTTCAAATATT[C/T]GAAAATAAAATCCAG	80013
rs549969036	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15836581	GAGACTAACACGTTA[C/T]TAGAGCTATGAGACT	80013
rs550042104	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15854905	GGTCCAACCTAGGAA[C/G]AAGAGATGAAATCTT	80013
rs550104524	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15831917	CTCACCTCAGGTGAT[C/T]CATCCACCTCGGCCT	80013
rs550149988	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15861121	AGAGTGTGTGGGCAA[C/T]ACCTGGACTAAAGTT	80013
rs550159173	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15842493	AATTTGTTTTGTATT[G/T]CACCTATTAATTTAA	80013
rs550202743	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15804316	ATATCTCCTTTTCAC[A/G]TAGCTCTGTATTATC	80013
rs550221892	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15830652	GAGATTGAGATTTTA[A/C]TCCAAAGATTTCTGT	80013
rs550240146	snp	C/T	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15784480	CCTCGTGAGGTGGCT[C/T]ATACCTGTAATCCCA	80013
rs550343123	snp	G/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15812890	CCCCTCCGCTGCCAA[G/T]CCAATCCATCACCCA	80013
rs550351451	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15795180	GTGCTTTCCACATTA[G/T]TCATTTAATATTCAT	80013
rs550353404	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15791049	CATTTTTAAGGTAGC[G/T]ATGAGATTTACAACT	80013
rs550367559	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15812275	AAATTTCAATGTTCT[A/G]TAATTTCTGGGAAAT	80013
rs550410754	in-del	-/CTCAGTTC	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15790931	AACCATAACCTGCAA[-/CTCAGTTC]CCACCCCAACCAAGA	80013
rs550416711	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15806282	AGTAACTCTGACCTT[A/C]ACAATGTAAGCTGCA	80013
rs550505240	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15812236	ATGAGCCCCTGCGCC[C/T]GGCCAATTCTTGATT	80013
rs550530753	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15818136	CAGAGAAATACACAG[A/G]ATCTGTGCCTGGTCT	80013
rs550537235	snp	C/T	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15783689	ATTTTTCATGTCTTA[C/T]ATTCCCAACTAAAGC	80013
rs550537840	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15833036	GTAATAAAGTGAAGG[A/G]AATTTTATTCAGTTA	80013
rs550633200	snp	C/G	0.00199481	0.0315187	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15860654	GAACTGTCTGGGACC[C/G]TTTGGTGGGGTGGTA	80013
rs550637922	in-del	-/AT	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15858333	ATGATTAAAGGTGGC[-/AT]AGAGCGTTCTAATAA	80013
rs550643695	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15859855	GGGGGTAAAGATGCG[C/G]AAGGCCACAGCACCC	80013
rs550666090	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15818639	TTAACATACAAAAGA[A/G]TATTATTTGCTCATA	80013
rs550667784	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15796317	GTGTAACGAGATAGG[C/T]CATAAACTCTCCAGG	80013
rs550676657	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15853182	ATTTTGTAGACTGAA[A/G]GGTGTGAATTAGAAA	80013
rs550702159	snp	A/C/T	0.000399281	0.0141238	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15861187	TCATGTGAAAACTTA[A/C/T]GTTTGTGCTGCTTAA	80013
rs550763163	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15792736	AAAGAAATGGTGTTG[A/C]TTCCTGACATATAAT	80013
rs550784932	snp	A/G	0.00279162	0.0372561	intron-variant	FAM188A	GRCh38.p7	10:15823466	CTACTAATAAGCCAA[A/G]CATTAAAGGGATTTG	80013
rs550819279	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15823966	CATTCACGTATACTG[C/T]AAATAACAGGATTTC	80013
rs550826094	snp	A/G	4.98533e-05	0.00499241	intron-variant	FAM188A	GRCh38.p7	10:15833603	ATTATTCATCAAAGA[A/G]AGCAACATAACAAGG	80013
rs550838657	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15856569	CACTCTCCCTCAGGC[A/G]TCAGCAAACTACAAC	80013
rs550842201	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15789554	ACTTGAGAACTCCGA[C/T]GAAAGCTTAAAGTCA	80013
rs550890198	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15851247	CTATATATTTTTCCT[C/G]AGTAATCTCATCTAC	80013
rs550953308	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15828331	TCACCAAAGACCGGA[C/T]AGCGTATGAGTCTAT	80013
rs551004338	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15816411	AGCATTTGACTTTAA[C/T]ACCATTGAATTATTA	80013
rs551023843	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15839580	AGACATAAAGATAAT[A/G]ATTTAGAGAAAAGAG	80013
rs551025264	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15832612	AGAAATCACCAAAAC[C/T]TGGCTCTCATTCTAA	80013
rs551061892	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15827607	AAAATATATCATTAA[A/C]AAAGTTAACAAGAAA	80013
rs551074403	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15825841	TGGCTGTAATACTGA[C/T]TTCTTTTTATAAAAA	80013
rs551074697	snp	A/C	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15802907	AACTCTTAATCACAC[A/C]ACTTAAAAAAGATGT	80013
rs551240370	snp	A/C	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15814060	AAATGTTAAAGAAGG[A/C]ATGGCCGAATAATGA	80013
rs551273867	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15839439	AAGTAATATTAACAA[A/G]AGGGGAAAACACTTT	80013
rs551284641	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15858407	AAACAACTTATTGTA[A/G]TTGTCAGGAAAAAGC	80013
rs551288438	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15794649	CTCAATTCTGAAAAA[C/T]TGCACTGATTATAAA	80013
rs551349777	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15786928	AAAAACCAAGGTTTA[C/T]AAACTCAAGCTTGTA	80013
rs551362109	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15789998	TTTAAACAAAAGTTG[C/T]TTATTCCTTAAATGT	80013
rs551429740	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15839970	CCCTTTAACCTATAG[C/T]AACGTGACGTATCAC	80013
rs551458489	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15783369	TTAGTCTTATCTCCA[A/G]CTACTCACCTTTCTG	80013
rs551472658	in-del	-/GACTT			intron-variant	FAM188A	GRCh38.p7	10:15799729	GTGACAGAAAAGGAG[-/GACTT]GACTTAGGAAGGGAA	80013
rs551480825	snp	G/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15788166	TTGTAAATTAGAGCA[G/T]TGTAAACAACATGGT	80013
rs551488000	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15843526	ATTTTCTGACAAGTA[C/G]AAGAACTAACTCACA	80013
rs551524255	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15781563	TATGTGCTTTGTCAA[C/T]GGTTAGCAAAGGAAA	80013
rs551596713	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15779458	TACCATCGGAAAGAA[A/G]TGCTTAATTATCATA	80013
rs551612150	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15797523	GTCCTTTATTGCTGG[A/G]CCCTTGAATTGTATC	80013
rs551726611	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15829273	CATTTTGGGGAAAGT[A/G]CCATTGTTTTTAACG	80013
rs551747629	snp	C/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15854703	ACTAAGAGAAGCACT[C/G]AGGGCTCAGCTAAGA	80013
rs551795073	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15815642	CCCAGAGATGTTTAA[C/G]GTATGTTTCTTGAAT	80013
rs551882092	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15857825	ATATCAAAAGAATTT[A/G]ACTTGATCAATCAAT	80013
rs551902409	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15849550	TGAAAGCAACATTAC[C/T]GTGGAGAAGAGAAAC	80013
rs551952415	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15820218	GGGGACAGTGAGCCA[C/T]CCATCTCAAGAGCTG	80013
rs551995047	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15832138	AATCCGGAGAACGCG[C/T]AGAAAGATGAACCAC	80013
rs552105357	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15831762	CTCACTGCAACCTCC[A/G]CCTCCCGGGTTCAAG	80013
rs552116853	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15798884	CTTGCCTGTGGTTCT[A/G]AACAGGCTATACAAG	80013
rs552151576	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15792264	CTGGCTCCCCAGTGG[A/G]CAATGAGTTCTGGAG	80013
rs552154669	snp	G/T			intron-variant, downstream-variant-500B	FAM188A	GRCh38.p7	10:15781987	CAATGCAGACTAACA[G/T]ATACTGGTCAAATCC	80013
rs552222103	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15861024	CTGCAACGCAGAATT[A/G]CAAGGTATTTGTAGG	80013
rs552263347	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15791022	TTATATATGATTAAC[A/C]TCAAGCTTAAACATT	80013
rs552295634	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15844107	ACTAACTAAAAATAA[A/C]TGTACAAACTTTAAA	80013
rs552345709	snp	C/T	0.00438332	0.0466095	intron-variant	FAM188A	GRCh38.p7	10:15813172	TTTTAACAAGTCTAG[C/T]TGTCCTAACTCTTAG	80013
rs552356196	snp	C/T	0.00199481	0.0315187	intron-variant	FAM188A	GRCh38.p7	10:15812985	CTACTCTGGACCAAA[C/T]TGTACTCTTTGCTTA	80013
rs552357550	snp	A/C	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15836036	TGTTCCAATTCTGAG[A/C]AGATGAAACCTACTC	80013
rs552375500	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15798232	TTTTTCTGGGTTAAA[A/T]CTTTTTGGGGGAAAG	80013
rs552399439	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	FAM188A	GRCh38.p7	10:15777933	CAGATCTCTCTCTCA[A/G]GTAAACGGGCTTCTG	80013
rs552442813	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15813475	TAAATTCTTACAGCA[C/T]TATGGACCTGTGCTT	80013
rs552472959	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15812176	GAACTCCTGACCTCA[C/T]GTGATTCACCTGCCT	80013
rs552492914	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15859972	GCCGAAGGGCAGCCC[A/G]GAGGATGGAAAGAGC	80013
rs552502717	snp	C/T			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15779487	TATTTACATATAATT[C/T]ATACAGGTCCTACTG	80013
rs552514596	snp	A/G	0.00279162	0.0372561	utr-variant-3-prime, nc-transcript-variant	FAM188A	GRCh38.p7	10:15778506	ATCCAGGTTGACAAT[A/G]TGTTATTTGTCAATA	80013
rs552556019	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15847659	CCTTGAAAATAAAGA[C/T]TGTCAAAAGGCTACT	80013
rs552562780	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15854970	AAAGGGACCCTAGTG[C/T]TGTACCCAAGTGCAG	80013
rs552569721	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15824845	GAACTATTTAGATTT[G/T]ATCAGTAAACACATG	80013
rs552572288	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15803737	AAACATGCTACTCTA[C/T]CTTTACTTCCAAGAA	80013
rs552641965	snp	A/G	0.00119737	0.0244387	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15784462	AAATAAATGTTTACT[A/G]GGCCTCGTGAGGTGG	80013
rs552655985	snp	A/T			upstream-variant-2KB	FAM188A	GRCh38.p7	10:15861073	CCTGTTTGTAAATGT[A/T]ACAGCATTTTCATCT	80013
rs552699495	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15804233	AGGGTTGGCGGGGGG[A/G]CGGGGGATGGAAGTA	80013
rs552709677	in-del	-/C	0.00358779	0.0422022	intron-variant	FAM188A	GRCh38.p7	10:15816980	ACTGCCTCTTATTTG[-/C]CCATAAATATCTGAA	80013
rs552717006	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15840723	TCCTGAAAAGCAAAT[C/G]AGAAAAGCAACTCTT	80013
rs552726614	snp	C/T	0.000399281	0.0141238	missense, downstream-variant-500B, nc-transcript-variant	FAM188A	GRCh38.p7	10:15782195	AATCCATTGTAGTGG[C/T]AGACAGTAAAAGATT	80013
rs552731429	snp	C/T	0.00398564	0.0444627	intron-variant	FAM188A	GRCh38.p7	10:15795846	GGTATTTTTCCCTGT[C/T]TGGGGTCAAGATTAA	80013
rs552742366	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15816131	CTGGGTGTGGTGGCA[C/T]GCACCTGTAGTCCCA	80013
rs552811842	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15781893	TTTAGAAACACGCTA[C/T]ACTGCCAAGGGTAAC	80013
rs552827315	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15846885	CCCACCACCACGCCC[A/G]GCTAGTTTTTTGTAT	80013
rs552834637	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15788427	AACTCATCTAAAAAC[A/G]GAACAAGACCAAATT	80013
rs552955210	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15847230	TTTTAACAATTTAAC[A/G]GTTTATAGCGAATCA	80013
rs552959991	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15827907	ACAATTCTAAGTGTC[A/G]GGCAGGATGCAGAAA	80013
rs552973507	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15803152	ATGTAATGTTTAAAT[G/T]TTCAGAGATGTAATC	80013
rs553054464	snp	A/G			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15783863	AACCATTTTCCTGTA[A/G]CTGAATATAATTTAT	80013
rs553074273	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15794071	CTGGGTTTATCAACC[A/T]GGGGTGGGAGCTAAA	80013
rs553126576	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15822547	GCAAAGTTTCCTTAA[A/C]TGTTTCTGGTCTGGG	80013
rs553140765	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15852015	CTTTCCGCTACTCTC[C/T]ATATAGATAAATCCT	80013
rs553177184	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15857583	AGCAGGAGGAAAGCA[A/G]AGAGAAGAATAAATT	80013
rs553210259	snp	A/C	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15846645	AAATATATTTTTAAT[A/C]ATGTAAGTATTATTA	80013
rs553236945	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15828526	TAAAATACTGAATTG[A/T]CCATTTTAAATGGGT	80013
rs553251882	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15856601	CTCATCTGCTTTCAT[A/G]TTTTAGAATGCAGCC	80013
rs553294209	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15794830	TTAATTTCAGTATCT[C/T]TGCAGCATTGATGAA	80013
rs553313855	snp	C/G	0.0376037	0.131863	intron-variant	FAM188A	GRCh38.p7	10:15845777	CTCCCAAAGTGCTGG[C/G]CTTACAGGTGTGAGC	80013
rs553321597	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15862106	CAATTCCTATCATCA[C/T]TGTATTTGCAAAGAG	80013
rs553340553	in-del	-/TATC			intron-variant	FAM188A	GRCh38.p7	10:15833942	TACATTTAACAACTT[-/TATC]TAAGATATATTTAAA	80013
rs553348783	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15859749	TACAAACAAAAAACT[C/G]CTTTTTGGAATTAGC	80013
rs553362563	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15855834	CTTTCCTATCTTTCA[C/G]GGTTGTTGCAAAGAT	80013
rs553399510	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15822881	GATACCCTTCAGCTA[A/C]CATACATTAATATAA	80013
rs553408659	snp	C/T			intron-variant, downstream-variant-500B	FAM188A	GRCh38.p7	10:15782342	TTGACTGGGGACTCA[C/T]TTGACAAAAGAAGGA	80013
rs553419410	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15831896	GGCCAGGCTGGTCTC[A/G]AACTCCTCACCTCAG	80013
rs553455831	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15801375	CAATCTTTTGGCTGT[A/G]TAAGAAAGAAGGCCT	80013
rs553463243	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15839065	TAGTCTTGGCTCCAG[A/G]GAGTTATTTATCACA	80013
rs553544937	snp	C/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15832462	ATTTTTTTTTTCATT[C/G]ACAGGATTAAATGCT	80013
rs553592160	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15826553	AATCTTCAAAGATTT[C/T]TTAAAACTGGAACTT	80013
rs553609528	snp	A/C	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15844206	CAATTCAAGGTGTTA[A/C]AACAAAAAACTAAGT	80013
rs553628895	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15850025	AGAAGAATATAAATC[A/G]TGAAGATTTCATGGA	80013
rs553719322	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15815362	ATCTTGCTCTATAAC[C/T]CCTATCTGGACTTTT	80013
rs553759768	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15821191	GTAAAATGCTTGAAA[G/T]TTTTTTCAGTGTGAA	80013
rs553793300	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15820662	AAGGGCAGGACAAAT[A/C]CAATTTGATTATCAT	80013
rs553832111	snp	C/T	0.00199481	0.0315187	intron-variant	FAM188A	GRCh38.p7	10:15814705	GGCTGCCATGGGACA[C/T]GCAGAAAACAGTATG	80013
rs553832556	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15840012	ATAGCATATTTCATA[A/G]TATGCACTCAGTATA	80013
rs553912462	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15831616	GATAATTGACTAATA[C/T]ATTCTGTACAGGAAG	80013
rs553937268	snp	A/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15818956	AAGCCCTGAATTGTA[A/T]GCTTTAAAATGGTGA	80013
rs553971036	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15792480	GCTGGGGATGCCTGA[A/C]AGAAACAGTGCTAAC	80013
rs554020985	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15805853	GAGCACACCTGCAGC[C/T]AACATGTAAGTTATG	80013
rs554058125	snp	C/T	0.00716266	0.059414	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15785430	ACAGGAATATTCTTT[C/T]TATTATAACTAAGAA	80013
rs554202083	in-del	-/GCTGTCCTAGTGGTC	0.00795532	0.062565	intron-variant	FAM188A	GRCh38.p7	10:15853465	AGACAGTAACATCAA[-/GCTGTCCTAGTGGTC]GCTGTCCTAGTGGTC	80013
rs554212167	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15830754	CTACGATTTTCGCAG[C/G]TAGTGAGGTCTTTGC	80013
rs554233708	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15853975	TGACATCACTGGTAA[C/T]AGAAACAAACGTGAC	80013
rs554274327	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15848830	CTGGATAACCCTGTG[A/G]AGATCATTTCACCTG	80013
rs554441582	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15859436	AGTTGTTTGCCTATC[C/G]AAACTTAAGAATTAG	80013
rs554522028	snp	C/T	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15797447	TGCTGATAATGTATA[C/T]GCCCAAGTGACATGT	80013
rs554541622	snp	C/T	0.00716266	0.059414	intron-variant	FAM188A	GRCh38.p7	10:15798711	TTTGAACCTGTGAGG[C/T]GGAGGTTGCAGTGAA	80013
rs554553837	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15821045	AATGGTTTAAATTCC[A/T]TTTAAAACTATTTAC	80013
rs554561795	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15852252	AACATACTGTGGCTA[C/T]TGCTCAATTAATGCT	80013
rs554634170	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15832327	TGAGATAAGATACCT[A/G]GGGGTCCAGAAACAA	80013
rs554661823	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15842064	ATGAGATGAGAGACC[A/G]TCAGCACATATGTTA	80013
rs554749802	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15842669	TTCACAGGAAATTGT[C/G]TAAGTGAAGGAAAGA	80013
rs554827400	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15858328	TTCTGCATGATTAAA[A/G]GTGGCAGAGCGTTCT	80013
rs554835908	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15846825	ACCTCCCAGGTTCAC[A/G]CCATTCTCCTGTCTC	80013
rs554872626	snp	A/C	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15823530	TTTGTTAAGTTTATT[A/C]AAAATGTTATTTATG	80013
rs554873105	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15840608	AAACTTTCCACAAAG[A/C]TGATAGTTAATGTGA	80013
rs554910273	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15818233	TGATGGATTTCCATC[A/C]CATCACATGGTGCCT	80013
rs554929380	snp	C/T	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15782774	ATGAAAACATACTTA[C/T]AATGCTTAAGGCGAT	80013
rs555000689	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15831367	TTCAGTGAAATATAA[A/T]TGGGGTATTTTTCTC	80013
rs555004755	snp	A/C	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15834031	AATATATAATTATTA[A/C]TATTTTGTCTTTGAT	80013
rs555012241	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15854423	ATTAAAGAGATTAGC[A/G]AAAATGTAAAACAAT	80013
rs555013662	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15821820	TGTATATATATTTAT[A/G]CTACACCAAAACTTT	80013
rs555083500	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15789089	TCAAGTCTGCTATAA[G/T]ATTGGATTAGTTCGA	80013
rs555248945	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15788536	ATTCTTAGAAAAACT[G/T]GCAGAAGGAAAAACT	80013
rs555313397	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15814592	TTGTGTTTTTCTCTT[A/G]ACTCCATGTCTCTAA	80013
rs555331458	snp	G/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15832363	AGAAGAAGAAAGACG[G/T]GAGTGTACAGAAGCC	80013
rs555411078	snp	A/T	0.00557542	0.0525036	intron-variant	FAM188A	GRCh38.p7	10:15851253	ATTTTTCCTGAGTAA[A/T]CTCATCTACTCCCAG	80013
rs555437774	in-del	-/CTAT	0.00199481	0.0315187	intron-variant	FAM188A	GRCh38.p7	10:15793762	GATGATGATCCCTGC[-/CTAT]CTATCTCCTAGGTTT	80013
rs555438996	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15801676	ATTGCTATTAAAGAG[A/G]ACCGCAACAGCAAGA	80013
rs555560393	snp	C/G	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15850196	TTAATCTCTTAATCC[C/G]GTCATCTTCGTAAGC	80013
rs555580971	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15781869	TCACTGGACTAACTA[C/T]GATGTTGATTTAGAA	80013
rs555598485	snp	A/C	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15779597	GAGGAACATGTGTCT[A/C]CTTCTAATTTAAGTA	80013
rs555610607	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15797854	CCCAAACCTTAGTTG[A/C]AGATTTCTACATTTA	80013
rs555616994	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15862019	TGCCAAACTTTCTCC[A/G]GTCATTACAATTGAA	80013
rs555648024	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15855753	AGACTTAGTTTGACA[C/T]CCTGGCTGAGTCAAA	80013
rs555671924	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15793496	TGAAATGGGCAGAAA[C/T]TGCTCAACTAGAAGC	80013
rs555686328	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15849966	TGAGTGAATGTTGCG[C/G]GAAGTTAGGGACCCT	80013
rs555855377	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15785341	AACCCTCTTTTTACC[C/T]AAAAAATTACTACAA	80013
rs555860048	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15838137	GTAGCGCATTTCTAT[A/G]TAAAACTAAGAACCT	80013
rs555885612	in-del	-/T	0.00279162	0.0372561	intron-variant	FAM188A	GRCh38.p7	10:15836954	TCAAAGGAAACACAA[-/T]TTGGAAGAAAGGACA	80013
rs555923714	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15834707	TACACTATAAACTAA[C/T]ACAATTATTTAAGTA	80013
rs555954712	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15844142	TGCAGCGAAGATTAT[A/G]TGAGAAAATCTATGT	80013
rs556032395	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15848805	GAAGTTAGGAGAACC[C/T]AGTGACCATCTGGAT	80013
rs556037721	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15813950	TTTCAGGCCACTGAA[C/T]GTATAATAAAGCAAA	80013
rs556067797	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15826493	GATAATATGTAAAGA[C/T]ATAATTTCCTCAAAA	80013
rs556068520	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15843392	CTTTTGACTAGTTCT[G/T]TAAAGATGTCAAATG	80013
rs556069622	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15820228	AGCCATCCATCTCAA[G/T]AGCTGGACAACTCCA	80013
rs556163364	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15861383	GGGTCATACTGGCCC[A/G]TATTCCTACCTTTTG	80013
rs556183457	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15830911	GATTTTTGTTTTAGG[C/T]AGTAGAAGCCACCTA	80013
rs556213869	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15824277	TCTTTTCTCTATCTT[C/T]GCCACACTTTTGTTG	80013
rs556288900	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15853917	ACACTTGTGTCCACT[A/G]CTGTGACTCTGACAG	80013
rs556325985	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15830167	GCCCTCAAGTGTTTC[A/G]ATTTTCTATAAAGGG	80013
rs556326112	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15823708	AATTTTCTTAAGCAT[A/T]GTGATCTTACTCTGC	80013
rs556339500	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15836370	AGACAGAAGACCAAA[C/T]GCCAAAACACACTGC	80013
rs556353102	snp	C/G	0.00517822	0.0506191	intron-variant	FAM188A	GRCh38.p7	10:15798516	GGCACGGTGTGTCAC[C/G]CCTGTAATCCCAGGA	80013
rs556368096	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15791375	AAGGAAACAGAGGCA[C/T]AAAGATGAAAAGACA	80013
rs556404793	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15839705	AAATAGATTGTTACA[C/T]GGAATAAAAATTGTA	80013
rs556493486	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15796537	ACCATTTTTTCCACA[C/T]TTTTTTGTTCAGGTA	80013
rs556518496	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15805202	GAAGTTAGACGACGT[C/T]CTTGGAGGTTCTTTG	80013
rs556597011	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15860108	CGACTGGGGCAGAGA[C/G]CGGGGCACGCGAGGG	80013
rs556613127	in-del	-/A	0.00199481	0.0315187	intron-variant	FAM188A	GRCh38.p7	10:15850488	AGAGAATGCATTCTC[-/A]GGGGGGAGGTCTCTA	80013
rs556620831	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15827112	ACAGAGCGAGACCCC[A/G]TCTCTAAAAAATGAA	80013
rs556622736	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15835566	GAGGAAGGGGATACC[A/G]TTTTAAAGACCAGGT	80013
rs556627822	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15818903	CATTTTGGAATTAGA[C/T]TGGGGTAATGGTTGC	80013
rs556628124	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15804659	TAAAAGGTAAATGCT[A/G]TATAATTTACCTTTA	80013
rs556699382	snp	A/C	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15783399	GAATTCTGTTTTGGA[A/C]AAGCATGACTCATTT	80013
rs556776861	snp	C/T	0.00279162	0.0372561	intron-variant	FAM188A	GRCh38.p7	10:15834987	GATTTTTTTAGATCA[C/T]GTAAAAACTTATTGC	80013
rs556796263	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15811566	TAAAGCAGTGGTATA[C/T]GTATTTGAATGTCAC	80013
rs556808837	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15780978	TCATCTGTAAAATAT[A/G]GATAATATTTGACCT	80013
rs556979114	in-del	-/T	0.0178098	0.0926698	intron-variant	FAM188A	GRCh38.p7	10:15829797	AGGGAGCAGCTAGCA[-/T]TTCTGTGCTTGCGCT	80013
rs557091478	in-del	-/T	0.00398564	0.0444627	intron-variant	FAM188A	GRCh38.p7	10:15814804	AAGTATCAGGACAGG[-/T]AGGAAGAGTGTACTC	80013
rs557200731	snp	A/G	0.00199481	0.0315187	intron-variant	FAM188A	GRCh38.p7	10:15824244	GTTTATATTCCCACC[A/G]ACAGCATATAGGAGT	80013
rs557254378	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15821391	AATAATAGATGTCTG[C/T]GGCTTTTTTGAATTA	80013
rs557256825	snp	A/C	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15846220	CCACTTGCAAAAATA[A/C]CTACCACTACTGAAA	80013
rs557256975	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15829121	TGATGCGAGGTGTAA[C/T]AGAATGAAGCCGACT	80013
rs557286113	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15839787	ACAAAGTATTTCAAA[G/T]GTATACATTATTTAA	80013
rs557288966	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15788451	CCAAATTCTAAAAAC[A/G]GTGTCTACCAATGTT	80013
rs557294187	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15823200	GAAGGTGCATATACA[A/T]ACAGTTTATACTTTG	80013
rs557314820	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15841226	AGAGATGCATTTTTT[G/T]TTGCAAAAATGTAGT	80013
rs557325450	snp	A/G/T	0.00199481	0.0315187	intron-variant	FAM188A	GRCh38.p7	10:15827800	CACAAACACGTGAAG[A/G/T]GATGATCAAGCTCAG	80013
rs557332124	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15850468	GCAAGGAACAGCCCT[A/G]AGAAAGAGAATGCAT	80013
rs557383863	snp	A/G			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15785309	ATGTCTGTTACAGGC[A/G]AAAGAGAAGGGACTA	80013
rs557393617	snp	A/G			upstream-variant-2KB	FAM188A	GRCh38.p7	10:15862393	CACAGAAGGGTCTAT[A/G]TACATAGAGCTCATA	80013
rs557393743	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15827199	AAAAAAAAAAAAAAA[G/T]CCCAAATAGAAGCCA	80013
rs557458093	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15815450	TGTCAATTCAGACTA[A/G]AGTATAATTTATACC	80013
rs557472617	snp	A/C/T			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15784067	TCTTCAATTTCCTCA[A/C/T]TGTCAAAAAATTCCT	80013
rs557506537	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15826675	GAATATCAAAGTATA[C/T]TATAAAACTATGTAA	80013
rs557509841	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15859860	TAAAGATGCGGAAGG[A/C]CACAGCACCCCTTGA	80013
rs557546182	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15801464	GTACCCTGCCAGTAA[A/G]AGACCACCTTTTAAA	80013
rs557546237	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15817977	CAATGTTGAGCCAGT[A/G]AAGTAGGAAGGATGG	80013
rs557570116	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15821313	GTGAAGCATATTCTT[C/T]GTTAGGTAATAAAGA	80013
rs557624770	in-del	-/A	0.00438332	0.0466095	intron-variant	FAM188A	GRCh38.p7	10:15853946	AGCTTCTCAATGCTT[-/A]CAGATTGTTCCGATG	80013
rs557632055	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15802149	TAGTAGTTAAATTTT[C/T]GAGGGAGTCAAAAGT	80013
rs557655924	snp	C/T	0.00119737	0.0244387	intron-variant, downstream-variant-500B	FAM188A	GRCh38.p7	10:15782069	AATCTTAGGTAGCAA[C/T]TGTACGGGAATCGAA	80013
rs557667775	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15832034	TGCCAATGAAAGTTA[A/T]CTCATCTCAGTCTAC	80013
rs557671513	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15809973	AATGTTATAAATGAT[C/T]AACCTGAACATTTTT	80013
rs557683974	snp	A/C	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15806299	CAATGTAAGCTGCAC[A/C]TGGAGGAATCTCCAC	80013
rs557685960	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15847236	CAATTTAACAGTTTA[C/T]AGCGAATCAGCCTTT	80013
rs557716101	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15850523	GGCCGCTCGGGGAGT[A/G]TCTTATACAGTTGTA	80013
rs557725272	snp	C/T	0.000123419	0.00785456	intron-variant	FAM188A	GRCh38.p7	10:15821770	ACGAAAACTTAGCAT[C/T]GTAGTAGTGTGTATA	80013
rs557744423	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15793141	TAATTCCTATAAAAC[A/G]TGTACCTGAATACGA	80013
rs557749155	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15844920	CCTGATTATTTGGCT[A/G]TAAAGCATCATTCCA	80013
rs557761828	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15815954	AAATAGCTTTGTTAT[A/G]AGAATTTTGAAATAG	80013
rs557836420	in-del	-/T	0.00199481	0.0315187	intron-variant	FAM188A	GRCh38.p7	10:15836212	CTCAATCCCTTACAC[-/T]TTTATACTTGCAGTG	80013
rs557847091	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15780467	ATTAAGTTAAATACA[A/G]TCGGCCCTATTTTTC	80013
rs557891267	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15845141	ATATTATTCCAAGGA[C/T]ACATTTGATATATGG	80013
rs557899435	snp	C/T	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15793898	GGTTTATGCTCCAAA[C/T]GATCAGTACTAAATC	80013
rs557905091	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15799959	GCAAGGGAAAATATT[C/G]AAAACTTATGGAAGC	80013
rs557949325	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15786272	GGGGTGGGAGTGGAG[A/G]AAGAGAATCTTTCTC	80013
rs557980633	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15834082	TCTTTCAGGCAGAAA[A/G]GTCTAAAAAGAAGGA	80013
rs558036329	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15861238	CCGAGCTTTGAATTT[A/G]AAACGAAAGGGCAAA	80013
rs558044086	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15830958	GGGAAGAGAATCACA[C/T]TTAATAGCAGAGACC	80013
rs558057109	snp	C/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15820200	TCTGCAGTCCAGCCT[C/G]AAGGGGACAGTGAGC	80013
rs558057512	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15784466	AAATGTTTACTGGGC[C/T]TCGTGAGGTGGCTCA	80013
rs558088008	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15799252	TTGCCCAGGCTGGAG[G/T]GCAGTGGTGTGATCT	80013
rs558120291	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15788212	AAGTTAGAAGAAGTA[C/T]AGTAATTACTATCAT	80013
rs558131911	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15784650	GCTGAGGCAGGAGAA[C/T]TGCTTGGACCAGGGA	80013
rs558169523	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15825851	ACTGATTTCTTTTTA[C/T]AAAAACAAAACAAAA	80013
rs558232676	snp	A/C	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15791292	TAGAAAAAGGCCAGA[A/C]TCATTAAGTGTAAAA	80013
rs558245347	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15814565	AGTTCTACACCCACA[A/T]GGCAGGAGTTTTTGT	80013
rs558257813	snp	A/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15844322	GTAGAAAAGTATAAC[A/T]ACATCACAACATTTG	80013
rs558272790	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15855660	ATATTACTTACTATA[C/T]ATATACACATTTTGC	80013
rs558311201	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15849917	TTCTTACCACACAAT[C/T]TACTTAACCCTCACT	80013
rs558395343	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15825313	CAAGCATGTACTCTA[C/T]ATTTGCAAAAAAATT	80013
rs558409580	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15860799	GAACATATGCCCATT[G/T]CTTGTATTTTTCAAT	80013
rs558410118	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15797794	GATTTAGGGAGCAAT[C/T]GCTGACATGTGGGTT	80013
rs558428060	snp	A/G	0.0023933	0.0345097	intron-variant	FAM188A	GRCh38.p7	10:15819466	CATTATAGGTCTCCC[A/G]CACTCCAGGGATCAC	80013
rs558442545	snp	C/T	0.00318978	0.0398085	intron-variant	FAM188A	GRCh38.p7	10:15848461	AACATGATGAAACCC[C/T]GTCTCTACTAAAAAT	80013
rs558494620	snp	C/T	0.00120144	0.0244801	intron-variant	FAM188A	GRCh38.p7	10:15848744	ATTACCCAACCAGCA[C/T]TGACTGATAGCAGCT	80013
rs558536485	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15860070	GGCGTGTCTAGAAAG[C/T]CCAGCTTCAGCGCTG	80013
rs558538389	snp	C/T	0.00318978	0.0398085	intron-variant	FAM188A	GRCh38.p7	10:15852866	AAACGATGGTTGGGT[C/T]TGTACTAAACATGTA	80013
rs558646848	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15835801	ATTTAATATTCCAAA[C/T]AGGTATTTATTTACA	80013
rs558705214	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15834901	AACTTTTAATAGGAG[A/G]AAGGAGAAATTATTT	80013
rs558741247	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15842722	ATGCAAATTCTTGTT[A/G]TTATAAGGTGGCACC	80013
rs558757306	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15798069	CAGTTATTCTTTCTA[C/T]TCGCCATCTGTTACA	80013
rs558767647	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15808380	TCTTGGAAGAGTAAA[C/T]GTATAAAGCACCACT	80013
rs558802440	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15830573	TGGCATGGGAGTTCA[C/T]CTTCTTTAAATTCCA	80013
rs558819048	in-del	-/T	0.00636936	0.0560724	intron-variant	FAM188A	GRCh38.p7	10:15804275	CTGTTAATGGGACTA[-/T]CTAATAGCCTACAAT	80013
rs558847486	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15848372	GGGCACAGTGGCTCA[C/T]GCCTGTAATCCCAGC	80013
rs558848782	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15797258	CTAAAACAAGGCAAC[C/T]TGTGCAAGCCCTTAC	80013
rs558853922	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15796327	ATAGGTCATAAACTC[C/T]CCAGGCCATTTATTT	80013
rs558904555	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15818313	ATTTAAATTAAGGTA[C/G]AAGTAAAAAAAAAAA	80013
rs558920699	snp	G/T			upstream-variant-2KB	FAM188A	GRCh38.p7	10:15861628	TGACTTTTTTACCCA[G/T]AAATTCTAGCCAGTT	80013
rs558936035	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15833070	ATCAGCTCTCCTTAA[C/T]GGAATGGATTGGCCA	80013
rs558963447	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15789000	TTTTAAAGTTTATAG[A/G]AAGACACTTTTAGCA	80013
rs558968600	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15856331	TCTTTTTTTCATATT[A/G]CGTAACAAAAATTGT	80013
rs559011346	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15823658	ATAATGATCAAGCCA[A/G]GGTATGAAGAGTATC	80013
rs559022429	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15839323	TGTGGGAAACAAACT[A/G]AAATTGAACCTGAGT	80013
rs559022833	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15819356	TAATATAGTTTTTCA[A/G]AAAATGCTGTCTTGA	80013
rs559034789	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15841927	CAGCATTTAAGCCAA[C/G]AGGTTTCCTCTACTG	80013
rs559048343	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15852621	CAACTATTACAAATG[C/T]TGCTGAATAAAGATA	80013
rs559055931	snp	A/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15783249	ATTCACCTGAGCTAC[A/T]CCTTCCCCTTCATGT	80013
rs559166566	snp	C/T	0.000286389	0.011963	intron-variant	FAM188A	GRCh38.p7	10:15841418	CAGGAAATAAAAATA[C/T]ATCTTACAAGAATGT	80013
rs559180377	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15796440	AACACTGGGGAAAAA[C/T]GTCTAATACAGGTAG	80013
rs559196337	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15789842	AAATGAAAGCTGTAG[A/G]TTTAAAAAAAACAGC	80013
rs559197926	snp	A/G	0.0023933	0.0345097	intron-variant	FAM188A	GRCh38.p7	10:15794417	ACATAGCTAAACCAC[A/G]AACAGTGTGATATTT	80013
rs559228527	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15815621	ACCTATCAAGTTACC[C/T]ATGATCCCAGAGATG	80013
rs559254261	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15795331	ATTTGCATGACATGG[A/G]TTTTCAGAGAGGAAA	80013
rs559256501	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15850541	TTATACAGTTGTAGA[C/T]AAGGGACGAAATAAG	80013
rs559296453	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15845958	TTCCCGAGTAGCTGG[G/T]ATTACAGGCGCCTGC	80013
rs559310706	snp	A/C	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15801129	CTTTGAGAAGAAAGA[A/C]TATCTGCCTGAACAG	80013
rs559397973	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15846435	TTGTTTCAGTTACTC[A/G]GTACAACAGCTATAA	80013
rs559430178	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15788013	CATGATTCAAGGTAC[A/G]TTTTCCATCTGATAA	80013
rs559474681	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15780232	TAGAATATATTACTA[A/G]ATCAGATAATCTTGT	80013
rs559545256	snp	A/G	0.00199481	0.0315187	intron-variant	FAM188A	GRCh38.p7	10:15856678	GCTGAGAGGCAATAA[A/G]AAGGCCACTCACCCT	80013
rs559583373	snp	A/G	0.0023933	0.0345097	intron-variant	FAM188A	GRCh38.p7	10:15830630	CCCCATTCATAGAGA[A/G]GAAGCTGAGATTGAG	80013
rs559629449	snp	A/G			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15779756	TAAAAAGGATGTCAG[A/G]ACAGAAAGAAAAGTA	80013
rs559631205	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15826884	TTCATAAATACAAAA[C/T]CCAGATAGACTAAAG	80013
rs559675272	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15853519	ACCCTCACACAACTA[C/T]AGAGCCAATTTAAGA	80013
rs559678048	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15827298	TGTAATCTCAGCACT[C/T]TGGAAGGCCGAGGTT	80013
rs559699154	snp	A/G	0.00279162	0.0372561	intron-variant, missense	FAM188A	GRCh38.p7	10:15780905	TCCAATCCCTGTTCT[A/G]CCAATGACTTGCTGT	80013
rs559718978	snp	C/T	0.00318978	0.0398085	intron-variant	FAM188A	GRCh38.p7	10:15804315	GATATCTCCTTTTCA[C/T]GTAGCTCTGTATTAT	80013
rs559798410	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15861482	TCATATATTGTAAGG[A/T]ATAAATGGAAAAAGT	80013
rs559825653	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15856216	TAAATACCCAAACAC[A/G]CCTTTAAACCTTAAA	80013
rs559837937	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15832135	GAGAATCCGGAGAAC[A/G]CGTAGAAAGATGAAC	80013
rs559850837	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15800296	AAAACAGGGGCATAC[A/G]GACTGTACCTGGCAC	80013
rs559905268	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15849490	AAAGGAAGAGAAGCA[C/G]GAAGAAGTTGTTTCA	80013
rs559919737	snp	A/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15806247	TATATTTTCCTCTTG[A/T]GTCTTCCCTCATGCT	80013
rs559961851	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15860923	CTGTCCGCCTCTGTA[C/T]TTCAATAAATCAAAG	80013
rs559974223	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15836485	TAGTCCCTAGCATAG[A/G]GTCAATCAACGCTCA	80013
rs560002014	snp	C/T	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15831738	TGGAGTGCCGTGGCA[C/T]GATCTCAGCTCACTG	80013
rs560010177	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15838166	CTTTCCACAGTATGA[A/G]CAGACTTAAAGTGGC	80013
rs560046738	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15819798	TCTCATTTAAAACCA[C/T]AGTTAACTGCTAAAA	80013
rs560069077	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15825576	TCAGTTTCTGACTGC[A/C]TTTTTAGGAGTTCCA	80013
rs560082228	snp	C/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15805707	ACATTATGCTAGCTC[C/G]TAGCAGAAACTTTAA	80013
rs560093655	snp	G/T	0.00636936	0.0560724	intron-variant	FAM188A	GRCh38.p7	10:15794971	TCTGATCCTTTCCTT[G/T]TATGTTTCTTTTCTC	80013
rs560098653	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15843611	CCCTGTAGAACACGA[A/G]CAAGTCTACATTTCA	80013
rs560107698	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15816298	AAAAAGAAAAAAAAT[A/T]AAAAAGACAAGAAAA	80013
rs560115530	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15845513	ACTCTTTTTTTTCCT[A/T]TTTAGAAACAGGGTC	80013
rs560150849	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15790817	GCACTCAAAATTTTG[A/G]AGGATCAACCTTTCG	80013
rs560170644	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15804543	TCAAAGAACCTCCAA[C/G]AGCATCGTCATCTAA	80013
rs560211327	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15842335	GTTCACTTTCTAATC[A/G]CCACAGTATTTATGA	80013
rs560348849	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15830532	CACTACATGTTAGTC[A/T]TGAGTGCTGTAATAC	80013
rs560393129	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15804809	ATTAGTGGCAGCAAG[A/T]TTAACAGAATTCAGT	80013
rs560407470	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15831014	GAAAGATATATAGTT[C/T]TTCTAAAACAGGAAA	80013
rs560471313	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15832491	CTTTCAGCTATGAAT[C/T]AGATTAAGGGTTGAA	80013
rs560471927	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15784369	TACTTGAAGCATTGT[A/G]AAGATTACCGAAGTT	80013
rs560508244	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15790910	GGCTGGCAGCCTTTC[C/T]GCAGAAACCATAACC	80013
rs560519746	in-del	-/TTAA	0.00159617	0.0282053	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15782677	TTTGGCCCACGATGT[-/TTAA]TTAGTGGTTTCTTTT	80013
rs560525712	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15823407	GGTTGATCTGTTATA[C/T]TGTATCAGACTAAAT	80013
rs560582284	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15797786	GGCTCTCAGATTTAG[A/G]GAGCAATTGCTGACA	80013
rs560590749	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15823772	TGTTTGTACTCTAAC[A/C]CACTCCCCTCATGCT	80013
rs560703318	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15829878	AAACCGAGGCTCAGA[A/T]AATTTAGCAGTTTGC	80013
rs560723878	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15783560	GGACACACTAGTTAG[C/T]TTTTTACTACACTGG	80013
rs560726532	in-del	-/A	0.00279162	0.0372561	downstream-variant-500B	FAM188A	GRCh38.p7	10:15777856	CTTTACACGTGGAGG[-/A]AAAAAAGTATTAATG	80013
rs560748264	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15796028	ATATCTTTTGAATAA[A/C]ATCAGGTCGCTATCA	80013
rs560748863	snp	A/G	0.00199481	0.0315187	intron-variant	FAM188A	GRCh38.p7	10:15848136	CACTCCCAAATGCAC[A/G]TAAGAGTACATATAC	80013
rs560764991	snp	C/G	0.00478085	0.0486577	intron-variant	FAM188A	GRCh38.p7	10:15804231	AGAGGGTTGGCGGGG[C/G]GGCGGGGGATGGAAG	80013
rs560783143	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15796790	TCTACCATGACTAAT[A/T]TATCACAGAAAACAT	80013
rs560785004	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15788793	CATCCCTAAAAGTTT[C/G]AGGTCAGTTAATTTA	80013
rs560910006	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15859202	GGGAGGGAGAGATTA[C/T]GTAAATCCTGAATTT	80013
rs560920074	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15834376	GAAATTAACATTTCA[C/T]ACATCAAGCAAACAA	80013
rs560923613	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15803347	TGTAGCAAACTTAAT[A/G]TTAATATATCAATAT	80013
rs560927451	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15805711	TATGCTAGCTCCTAG[C/G]AGAAACTTTAAGTGC	80013
rs560950045	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15824598	TCATATCTTCGCAAA[C/T]TTTTCTCTCCCTTTC	80013
rs561053107	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15855777	AGTCAAATATCTCAA[C/T]TGGACTTCACATCTA	80013
rs561081019	snp	A/G	0.0023933	0.0345097	downstream-variant-500B	FAM188A	GRCh38.p7	10:15777729	ATTGTGTGTGTGTAC[A/G]AAAGAAAACAAAACC	80013
rs561081394	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15829387	CCAGATTCCAGCTGA[C/T]AACAATTCCATTACA	80013
rs561117199	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15838573	TACTGATAATCAGTG[C/T]CTCACATATCATAAT	80013
rs561124191	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15801201	GGAAATGCCATAAAG[C/G]ACATTTATAAGTAAG	80013
rs561183455	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15795787	TTCGTTTGGATAAGT[A/G]AAGAAGAAAATGATT	80013
rs561202745	snp	C/G	0.0023933	0.0345097	intron-variant	FAM188A	GRCh38.p7	10:15839862	ATACAAAGTAAACTG[C/G]AAAAATTACTAAAAT	80013
rs561206403	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15857768	GTCAAGCCAATTAAA[A/C]ACAACTATGTGCCAC	80013
rs561241161	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15809569	GAAAGTTCTCCATCG[A/T]ACTTAATAGGAATTA	80013
rs561245665	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15802761	TCCAAATAACAAAAC[C/T]ACCAACTGTAACTGT	80013
rs561329599	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15825326	TACATTTGCAAAAAA[A/G]TTCAAATTACTTTGT	80013
rs561340694	snp	A/T	0.0023933	0.0345097	intron-variant	FAM188A	GRCh38.p7	10:15851619	ACGTGTCCATTTCCA[A/T]CCCATCTCCAGTCCA	80013
rs561365692	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15839259	AGTGTTTCATATTTC[A/G]TTTTAAAATCTTTAG	80013
rs561378479	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15832549	CTGAGCAAGATAATT[C/T]GTAGTTTTTTGTTCA	80013
rs561413205	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15822805	TTATGGAAGTGGGTA[A/T]GTCAGAACAGACACA	80013
rs561442182	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15845435	CTGGTCTCCTTAATA[A/G]CTTAGTTTTGACTCT	80013
rs561468170	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15827490	AGAGGTTGCAGTGAG[C/G]CAGGATCGTGCCACT	80013
rs561477498	in-del	-/TAAA	0.00119737	0.0244387	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15783843	TAAATTATTTGAACT[-/TAAA]TAACCATTTTCCTGT	80013
rs561489057	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15816176	TGAAGTGGGAGAATC[A/G]CTTGAACCCAGGAGA	80013
rs561492846	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15787943	GTGAATACTTCAGTC[C/T]AATCTTTCAACTACT	80013
rs561551102	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15828193	CACTCCACATGTTGG[C/T]GAACAAATGAATGTG	80013
rs561605388	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15826816	TGACTGGAATTAGGA[C/G]ATTAGATAATTCTTT	80013
rs561616222	snp	A/G	0.0023933	0.0345097	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15783107	GCTGCTGGCAACTGG[A/G]GCTTCAGCTCCTACA	80013
rs561618129	snp	C/T	0.00398564	0.0444627	intron-variant	FAM188A	GRCh38.p7	10:15810386	ACATGTTACAGCATA[C/T]AGGTAGTTTCACAAA	80013
rs561669140	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15832985	GGTTACTTAATGTAA[A/G]TTAAATGAATAAATA	80013
rs561680947	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15832579	ACGAATTTCACTGTT[C/T]AAACTCTGACCTTTA	80013
rs561701594	snp	A/C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15794303	ACAAAAGCATATCAT[A/C/T]TGGGGAAAGAAAATT	80013
rs561748835	snp	C/G	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15813195	ACTCTTAGTATCAAA[C/G]AGTAACATGGCCTGC	80013
rs561765831	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15826139	GAAGATGGATGGCAG[A/G]TAGAGAGGAGAAAGA	80013
rs561778572	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15800502	CCGCATGTGCAGCCC[A/G]TCACTCCAGTGAGTT	80013
rs561791956	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15815520	GACTATACATGCTCA[A/G]AAAGCTCAAGGAGTA	80013
rs561818428	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15850516	CTAAAATGGCCGCTC[A/G]GGGAGTGTCTTATAC	80013
rs561832716	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15807777	CTGACATCACTGATG[A/G]CTGAGAAGTAATAAG	80013
rs561855874	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15848823	TGACCATCTGGATAA[C/G]CCTGTGAAGATCATT	80013
rs561905818	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15803852	ACACAAAAAACCCCA[C/T]GAATGATAATTAAGT	80013
rs561941561	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15788726	GAGAATGAAGACAAT[C/G]ACAGGATCCTAAGAA	80013
rs561942637	snp	G/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15779317	CTTACTGATTAATGT[G/T]AAAGTAAATTTGTAA	80013
rs561977929	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15791903	GAGCCTAGCAGGTCT[C/G]AATTTTAACAGAGAT	80013
rs561983122	snp	A/G	0.00119737	0.0244387	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15779968	TGTGGACATTAAGGC[A/G]CTCCTTGGTGGTTAA	80013
rs562073393	snp	C/T	0.00398564	0.0444627	intron-variant	FAM188A	GRCh38.p7	10:15831679	CCTCCTTTTCTTTTT[C/T]TTTTTTTTTTTTTTG	80013
rs562125019	snp	A/C	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	FAM188A	GRCh38.p7	10:15778288	TATAAATATAGAAGA[A/C]AGCTGGCTTACAGGG	80013
rs562157844	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15786361	GTCTGCGTCATCTTC[C/T]GCTGCCCTCCCCATC	80013
rs562214225	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15813208	AAGAGTAACATGGCC[G/T]GCTATTCTTCCAGCT	80013
rs562230276	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15849403	AAGAACCAGGACTTA[A/G]CCAGCAGAGATCTTT	80013
rs562232117	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15843897	CAACGGTAGCTATAT[A/C]CCAGTCACCTGACTT	80013
rs562272511	snp	C/T	0.00279162	0.0372561	intron-variant	FAM188A	GRCh38.p7	10:15844413	CATGCTTCCTTCCCA[C/T]CTTTTTTAATATCTA	80013
rs562278501	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15836977	AAAGGACAGCATTTC[A/G]CAACCAGAACATTAT	80013
rs562313614	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15836582	AGACTAACACGTTAC[C/T]AGAGCTATGAGACTG	80013
rs562316827	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15860846	TAGAACTATAAGGCA[A/G]TAGTTGAGTCACAGT	80013
rs562320621	snp	A/C	0.000798403	0.0199641	intron-variant, stop-lost	FAM188A	GRCh38.p7	10:15786456	TGTTTTCTCAGTCTC[A/C]TATCTGCGCATTAGG	80013
rs562364219	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15849097	AATAAACTAATGTTA[C/T]AAGAGAAGAATGCAG	80013
rs562400290	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15794389	TTTTAATCCTTCTTA[C/G]AGCTGACTATACACA	80013
rs562433629	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15842771	AGAAGCTCATGTTAC[A/T]GAAGCTATGACAGCT	80013
rs562476938	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15853683	GATGGTCAAAAGTTA[C/T]CTCAAGGAAAAGTAT	80013
rs562481385	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15831751	CATGATCTCAGCTCA[A/C]TGCAACCTCCGCCTC	80013
rs562527592	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15824705	ATTTCTAAAATCAGT[G/T]ACCACCACCTAGTGT	80013
rs562548687	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15842272	GATACAAGGAGGTTT[C/T]TGTCTCTCCTAATGG	80013
rs562561549	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15830447	AGTTTAATAAATGGC[A/G]CAACTGAGATTCCAA	80013
rs562588570	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime, nc-transcript-variant	FAM188A	GRCh38.p7	10:15860442	AAGAAGGGGCTGAGA[A/G]CCACTTGCAGAGACC	80013
rs562616662	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15789975	GGGTAGTTTGAAATG[A/G]GAGTGGTTTTAAACA	80013
rs562618172	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15819109	GAAAGAGATTATTTC[A/G]TCACCTTAATTGTAT	80013
rs562618287	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15825412	ACGGTGTCTTGCCTT[C/T]TTGCCCAGGTTGGTT	80013
rs562793483	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15835200	TAAAAACCAATTTCC[C/T]GATACTTTTTAAACC	80013
rs562800330	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15822923	GGTCCATAATATATC[C/T]AAAAAGCATTTCTTT	80013
rs562816143	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15818326	TAGAAGTAAAAAAAA[A/C]AAACAAACAAACAAA	80013
rs562820533	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15852938	AACAACTATTTGCAT[A/G]GCATTTACAGTGTAT	80013
rs562822099	snp	A/T	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15790283	TAAACCTCTTTTCTA[A/T]TCTTAAACCTCATAA	80013
rs562834396	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15830027	CGAGAATGGAGAATC[G/T]CGAAGACTCAGCAAC	80013
rs562849171	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15812028	CTCACTGCAACCTCC[A/G]TCCCCTGGGTTCAAG	80013
rs562877752	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15859187	AACAAACATGTGGGA[C/G]GGAGGGAGAGATTAC	80013
rs562894319	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15823309	GACCCTCTTAGAGAC[G/T]ACGTGAGATCAACAT	80013
rs562907997	in-del	-/TCT	0.00438332	0.0466095	cds-indel, nc-transcript-variant	FAM188A	GRCh38.p7	10:15778250	TAATGTAATAACAGA[-/TCT]TCTCATGCATTTATC	80013
rs562920343	snp	A/G			upstream-variant-2KB	FAM188A	GRCh38.p7	10:15861859	AATTTTATTTCTTCA[A/G]TACCCTTTACTGTAA	80013
rs562966030	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15828897	ATTAAATAGTTACTC[A/G]TTGAAAATCCTTAGG	80013
rs562969327	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15811222	AACATAATTCACAAT[A/G]AAACCGAAGTTGAAA	80013
rs563010040	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15783027	CTTCCTGGCCATATC[C/T]GATGGATACAAACAG	80013
rs563139029	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15852443	ATCTTAAACATGTCA[A/G]TTAAAGTGAATGAGA	80013
rs563139711	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15801849	CCAATCAGAGTAAAG[C/G]GTTTCAAGATAAAGA	80013
rs563159778	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15834314	AAATACCTCCCCACT[A/G]TTATCTTAAAACAAA	80013
rs563176626	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15802588	GGACAAAGCCAAATC[A/C]TATCAGGAATTAAGG	80013
rs563249883	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15808995	ATTATGTCTTCCATT[G/T]TATACATTCTAAATT	80013
rs563252308	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15788754	GAAAATACTGAAAAA[C/T]GATATGCCATAATAT	80013
rs563278484	snp	A/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	FAM188A	GRCh38.p7	10:15782430	TGAAGAAGATGCTGG[A/T]AAGTAGGGAAGGTTG	80013
rs563293735	snp	A/T	0.00438332	0.0466095	intron-variant	FAM188A	GRCh38.p7	10:15781394	AGCTATAACTAATAC[A/T]TATATATTATATATA	80013
rs563325759	snp	A/C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15781922	ACGATCTGTATGGGG[A/C/G]TGTATTTAGTCATGG	80013
rs563334687	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15809881	AGATGACTCTTTCTA[C/T]ATCAGACAGAAAATA	80013
rs563356935	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15852966	TATTAGGTATTGTAA[A/G]TAATCTAGAGATTAT	80013
rs563369293	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15795385	AGTTTCAAGACAGAA[C/G]AAAGTAAAGATAACT	80013
rs563388113	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15840776	TGTCTCCATTTCACA[A/C]TGGCAGCTTTCGGGT	80013
rs563411527	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15781075	AAACATCAAACTCTA[A/G]ATGAAGCACTCATTC	80013
rs563417006	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15795892	ACACCTTCAGTACTC[A/C]AAGAAACACAGAAAC	80013
rs563431292	snp	C/T	1.65176e-05	0.00287376	synonymous-codon, nc-transcript-variant	FAM188A	GRCh38.p7	10:15833682	AGAAACAGCATGTCC[C/T]GTCAGCAGGAGATTA	80013
rs563440404	snp	G/T	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15851551	CAAACTTACCTATAG[G/T]TTTCACCCTAAGATA	80013
rs563477732	snp	C/G	0.00199481	0.0315187	intron-variant	FAM188A	GRCh38.p7	10:15846916	TTTTAGTAGAGACGG[C/G]GTTTCACCATGTTAG	80013
rs563514507	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15800128	AATTTGTGACAATTT[A/G]AAAAACTCGCAAACT	80013
rs563519188	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15815676	AAAAATGATGATGAT[A/G]ATGATGATGACGATG	80013
rs563595796	in-del	-/AAAT	0.00874735	0.0655527	intron-variant	FAM188A	GRCh38.p7	10:15801905	ATACCACATCAGAAG[-/AAAT]AAATAACAGAAGATG	80013
rs563685593	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15822046	GTTGACAAAAATACA[A/C]GAAGAAAAAGAGACT	80013
rs563686327	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15786432	TCTGGGAAGGTTTCC[A/G]TGTAACGGTGTTTTC	80013
rs563710559	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15820091	CAAGATTTAAAAAGA[A/C]AAGTAAACAAAAAGT	80013
rs563723935	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15858006	TGTCACATTAGTAAT[G/T]CAGCAAAGCAGTGTC	80013
rs563813374	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15855954	ATATATTCAAAGTAC[A/C]AAGGAATTAATTTTG	80013
rs563818445	snp	C/T	6.69736e-05	0.00578639	intron-variant, utr-variant-5-prime	FAM188A	GRCh38.p7	10:15838283	CAGCCAAGGCAGCTA[C/T]ACATAAAAGACACTT	80013
rs563819219	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15849558	ACATTACCGTGGAGA[A/T]GAGAAACTACATTCA	80013
rs563844565	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15793626	AAGATACTGGTAGTA[C/G]AGAGAAGGGGAAAGA	80013
rs563861303	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15794239	ATGCTTGTAAGAACT[G/T]TCTGCATACTAAGTG	80013
rs563862451	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15860127	GGCACGCGAGGGGCT[A/G]GAGCGAGAGGCGTCA	80013
rs563894837	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15832510	TTAAGGGTTGAAGAA[C/T]AGGATGATCTCAATT	80013
rs563927443	snp	C/T			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15782503	AATTATGTGCATGTA[C/T]CACTATAACTTTTTT	80013
rs563988720	snp	A/G			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15779201	CAAATTCTTATGTGG[A/G]ATGAAAACAATTTTT	80013
rs564026248	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15823164	GTTTAACTTTCTGGA[C/T]TGGTAAATCCAAAAT	80013
rs564036647	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15839207	TATTTACAATTTAAA[A/T]TGTCACATTATGCTA	80013
rs564062162	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15807198	TAAACACTCACAGTA[A/G]ACTATTACCATGTAT	80013
rs564065287	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15853805	CAGTTATTCAGACTT[A/G]AGTATCTGGCTGACA	80013
rs564068812	snp	C/T	0.00755907	0.0610114	intron-variant	FAM188A	GRCh38.p7	10:15833506	AAACTGTAAAGGATT[C/T]TTCTATTAGAAAACA	80013
rs564092723	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15845718	CACTCTGTTGCCCAG[C/T]CTGGTTTTGAACTCC	80013
rs564099170	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15800391	TAACTTTAGTGCATA[C/T]TGTACTACTGGAATA	80013
rs564172693	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15820720	ACATGAAAAAGGAAC[A/G]CTGTCTGACGAAAAA	80013
rs564257770	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15779209	TATGTGGAATGAAAA[C/T]AATTTTTAGAGGCTA	80013
rs564268772	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15840833	AAAAACCACAGAATA[C/T]ATAATTTTTATGAAT	80013
rs564351910	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15785561	ATCCAGTCAGAATGT[A/G]AACAAAGAGGATATC	80013
rs564397922	in-del	-/T	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15811570	GCAGTGGTATATGTA[-/T]TTGAATGTCACTGAT	80013
rs564441419	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15798712	TTGAACCTGTGAGGC[A/G]GAGGTTGCAGTGAAC	80013
rs564518158	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15837041	AAACTGCTTAAGCAA[C/T]GAGTGAGTGCTGAGG	80013
rs564524547	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15784172	TGTCAAAATGGGGAA[A/G]ATAATAGTATGGTGT	80013
rs564589998	snp	G/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15819055	CTTATTCTTTGTTGG[G/T]TTTGTACGTGTGTGT	80013
rs564672838	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15848994	CAATCATCTAGGATA[C/T]ATGCCTGGATGACAC	80013
rs564701982	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15824615	TTTCTCTCCCTTTCC[G/T]TCTTAAATGTAAGCA	80013
rs564715312	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15845953	TCAGTTTCCCGAGTA[G/T]CTGGGATTACAGGCG	80013
rs564731052	snp	G/T	0.00279162	0.0372561	intron-variant	FAM188A	GRCh38.p7	10:15798239	GGGTTAAATCTTTTT[G/T]GGGGAAAGGTAGTAG	80013
rs564747389	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15783135	ACAGAAAGATAGGCT[A/G]TGAGAATGTAGCCAC	80013
rs564770574	snp	A/G	0.00012181	0.00780322	utr-variant-5-prime, nc-transcript-variant	FAM188A	GRCh38.p7	10:15860333	GGATCTTCGCTTTGC[A/G]GACTCCTGCCCCGGA	80013
rs564854206	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15859838	AATAGACAGCTCTGT[C/T]AGGGGGTAAAGATGC	80013
rs564900641	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15852317	TTTGTTTCTAGGAAT[A/C]CCAAGTTCAGTCTCA	80013
rs564923847	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15829955	ACCCGAGGCCTCTGC[C/T]TGTTCCACCATGGCA	80013
rs565031856	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15823911	TGATTTTGTCTTTTT[C/T]TTCCTGGCTTATTTC	80013
rs565045451	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15804164	ACTGGTCAACAGGGA[C/T]TGCAAAACAATATAG	80013
rs565077933	in-del	-/A	0.00993419	0.0697739	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15782479	CAGAACTAACTTATT[-/A]TTTTTTTTAATTATG	80013
rs565096619	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15847022	GCCACCGTGCCTGGC[C/G]AGAATGCATTCTTAA	80013
rs565110963	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15815979	AAATAGAAATATTCA[G/T]ATATGGCGGGGCACA	80013
rs565125606	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15842992	TTTTACCAAGAGGCC[A/G]AACGTTTTTCCCTTA	80013
rs565173615	snp	A/G	1.7403e-05	0.00294978	intron-variant	FAM188A	GRCh38.p7	10:15841643	TGGTTTCCTCTGGAA[A/G]AAAAAAAATTCTGTC	80013
rs565178523	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15858375	GTTCTATTTAGAATA[A/T]TGATTAGCCATCAAA	80013
rs565190843	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15833553	TGTAGAGCCATTAAA[C/T]AGACGAATAATAATC	80013
rs565206011	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15828353	TGAGTCTATTTCTAT[C/G]AAACATCTCAAACAG	80013
rs565215923	snp	A/G	0.000183158	0.00956793	intron-variant	FAM188A	GRCh38.p7	10:15834515	AACTGGAGTTCACAT[A/G]AGGAGACAAGAGATT	80013
rs565234950	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15817562	AAAACTTGAGAACAC[A/G]ATTGTGTGTGTGTGA	80013
rs565283400	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15856489	GACTAGTCTTTAGGA[A/G]AAACAATAAAATAAC	80013
rs565309920	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15803461	TCAGAGGTATAACTG[A/C]CGTATTTTTCTTATT	80013
rs565318116	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15853232	GGAAAAGAGGAAGTT[C/T]AAGGTCTCCAAGTCC	80013
rs565333871	snp	A/T			utr-variant-3-prime, nc-transcript-variant	FAM188A	GRCh38.p7	10:15778219	AACTAGGATCATAAT[A/T]AATAACGTAATATAC	80013
rs565465533	in-del	-/C	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15792888	GGAATAAGCTCTGTG[-/C]CACACATTTTTTAAA	80013
rs565481159	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15822276	AAATGATCTCTGCCT[C/T]AGAAAGGCTATGACT	80013
rs565539438	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15838635	TATATAAATCCAAGT[A/G]ATATCATCAGAGCTA	80013
rs565554692	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15821201	TGAAATTTTTTTCAG[C/T]GTGAAATCATTTTTC	80013
rs565643248	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15807341	AGGAGCAACAAGAGA[A/G]TAGGAGAATCAGCGG	80013
rs565664198	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15827154	TGGGGGTGGGAGACA[C/T]ATAAAATTGATATAA	80013
rs565666381	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15781526	TTTACGCCAGGTTGA[A/G]TACACCTGGCAGTGA	80013
rs565700114	snp	C/T			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15783443	TCTTTTGTTGGCCTT[C/T]TGCACATTCATGATT	80013
rs565713249	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15814470	TAATTCCCCCCACCC[C/T]TAGTGTGCCAGACTA	80013
rs565787561	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15848088	GGATCAAGGAACCTT[A/T]TGAAAAAAAAATCTA	80013
rs565795738	snp	C/T	3.30633e-05	0.00406578	missense, intron-variant, nc-transcript-variant	FAM188A	GRCh38.p7	10:15786580	TCAGGAAAAAATTCT[C/T]GAAGAAATGGGCCCA	80013
rs565831393	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15845529	TTTAGAAACAGGGTC[A/T]CCCTCTATTGCCCAG	80013
rs565841154	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15799825	ATCCAAGTAGAATAC[A/G]TGGAGTTATCTTAAT	80013
rs565859444	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15800735	TGTGGTTGCTCACTA[C/T]GTCAAGATAAATGAA	80013
rs565871410	in-del	-/CAAA			downstream-variant-500B	FAM188A	GRCh38.p7	10:15777745	AAAGAAAACAAAACC[-/CAAA]CAGAAATTCACACAG	80013
rs565895127	snp	C/G	0.00835141	0.0640778	intron-variant	FAM188A	GRCh38.p7	10:15836100	CTAAGTCTTTTCTTA[C/G]ATATGTGCCCAGTCT	80013
rs566031855	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15855511	AACACCTAATCCTAC[A/G]TAGACAATTTTGTAT	80013
rs566081965	snp	C/G	0.00874735	0.0655527	intron-variant	FAM188A	GRCh38.p7	10:15816379	TTAAAATTGTGGGAA[C/G]TATTCCATCTTAAAA	80013
rs566117515	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15826206	ATTTTATTTTAAGTG[C/T]GTAGGGAAGCCAGCC	80013
rs566150352	in-del	-/TTAATA	0.00358779	0.0422022	intron-variant	FAM188A	GRCh38.p7	10:15803342	ATCCATGTAGCAAAC[-/TTAATA]TTAATATATCAATAT	80013
rs566260627	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15811500	ATTTTGGAAGTGATA[A/T]TCACTTCTAACACAA	80013
rs566288855	snp	G/T	0.00517822	0.0506191	utr-variant-5-prime, upstream-variant-2KB	FAM188A	GRCh38.p7	10:15860511	CGTACCGGAAGTGCT[G/T]GTGCCACTTCCGACT	80013
rs566307390	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15861202	TGTTTGTGCTGCTTA[A/T]AAAAAGAGGGCTTGT	80013
rs566332989	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15798455	ATGCCTTGTCTCTAA[C/G]TGCCAAGTGTTTTTT	80013
rs566374998	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15836778	GTAACAGATAAAGAA[A/G]GAAACAAAGCTATCA	80013
rs566401768	snp	A/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15831294	TTTCTAGCAATAATC[A/T]GCCTGGCAGTGGGAG	80013
rs566411355	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15832512	AAGGGTTGAAGAATA[C/G]GATGATCTCAATTAA	80013
rs566429840	snp	C/G	0.00279162	0.0372561	intron-variant	FAM188A	GRCh38.p7	10:15848717	TTATATTGGCTTTAC[C/G]TTAATTTAAATATTA	80013
rs566444172	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15805101	TCTTGTGCCATAATT[A/G]TTAAAATCATTAATG	80013
rs566445488	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15860022	AGCTGTAACCATTCT[C/T]CTACTCAAACTCTCC	80013
rs566475034	snp	A/C	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15844060	CTGCTTTTTATCAGG[A/C]AAACTTAGGTTTGAA	80013
rs566487655	snp	C/G	0.00398564	0.0444627	intron-variant	FAM188A	GRCh38.p7	10:15798813	AAAAAACCACTATGC[C/G]AACGTAGAAAGAAAT	80013
rs566509468	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15797537	GACCCTTGAATTGTA[A/T]CTAGTCTTCTGCTAT	80013
rs566528969	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15804493	TCTCATTAAGCCTTT[A/C]ATCGTTATGAAGAGC	80013
rs566540748	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15812938	CAGGAGTAAATCTCT[A/G]AAATCCATGCACTTT	80013
rs566602191	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15824148	TTGGGTAGATACTGA[A/G]TAGTGGGATTGCTGG	80013
rs566613844	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15853321	GAGACCTTTCAGGGG[A/G]CCCACTGGAAGTTAC	80013
rs566644178	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15802098	GTGTTAATCTACTGT[C/T]GGTTACGGTAAGGCT	80013
rs566651152	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15819167	GCAAAATGTTAATTT[A/C]ATCTTTAAAGGGAAA	80013
rs566652971	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15812343	TATTACTCACAACAT[C/T]TTTTACTTTATTAAT	80013
rs566656678	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15829581	TGCTAAGAAGCTGAA[A/G]CTTTAGTTGGCAAGC	80013
rs566659115	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15835351	ACTTAACTTTAGCCA[C/T]TGTTTCTATCATATT	80013
rs566698817	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15841344	ATGAAAATTTTAAGT[A/C]ATTTTTTCTTCAAAA	80013
rs566718033	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15826494	ATAATATGTAAAGAT[A/G]TAATTTCCTCAAAAT	80013
rs566723128	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15859467	GGATAGTTACTAGTA[C/T]AAAGCGCCCAGCCTG	80013
rs566733428	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15841863	ACTAAACATTATGAA[A/G]GATCATAATGTGACA	80013
rs566765195	snp	A/C	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15783839	GAGTTAAATTATTTG[A/C]ACTTAAATAACCATT	80013
rs566783554	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15787282	CAATGCAGGTGTACC[A/C]AGGCTGGTGACAGGT	80013
rs566822320	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15790451	TACTGAGAATAAAGA[C/T]GACCTTGGTTGAAGG	80013
rs566829902	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15834098	GTCTAAAAAGAAGGA[C/T]TCACGTATTAGAGTA	80013
rs566857936	snp	C/T	0.00119737	0.0244387	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15783217	CCAGGAGCACTTTCC[C/T]GGTGCTTGCTTCTTC	80013
rs566872057	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15823554	ATTTATGTTAATATT[A/G]ATGAGTATATTTTGT	80013
rs566902453	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15817168	TAACACAGCTGGAGA[C/T]AACTATTTAGCCCTA	80013
rs566924277	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15847630	CTGAAAGTCAGGGAA[C/T]GCCTATTATTTTTCC	80013
rs566943078	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15788959	CATAAAATTTTAAGA[C/T]GTGGGGAAGTGTTTG	80013
rs566943100	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15803701	TGTGCACTTAAGGTC[A/G]CAGTCTAATAGAACA	80013
rs566953669	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15826197	GGAGTTTGGATTTTA[C/T]TTTAAGTGCGTAGGG	80013
rs566999986	in-del	-/AACT	0.00279162	0.0372561	intron-variant	FAM188A	GRCh38.p7	10:15840594	TAATCTCTTTACGAA[-/AACT]TTCCACAAAGATGAT	80013
rs567039355	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15852524	GCTGAGTCAGCAAAG[C/G]AGACTGATAAACATT	80013
rs567053322	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15811334	TAATCGCTGAGACCT[C/T]AGTTCATCCTGTATA	80013
rs567060723	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15796417	TGGAGTTTTACATAA[A/T]TACTTAAAACACTGG	80013
rs567141477	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15847200	ATTACAGTAAACTGA[G/T]AATTCAATTCTTGGT	80013
rs567153902	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15803097	ATGCTTTTTGGATCA[C/T]TGTAGAAAATGATCT	80013
rs567203357	snp	G/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15828960	CTTCTTCATAACATA[G/T]GGAGTAATACTTGCC	80013
rs567231154	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15858570	CCTCACAATAACTCT[C/G]TAAGGTCTATTATCT	80013
rs567301069	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15851988	TCACTGTTCTCTCTA[A/C]ATAAAAATGCTCTTT	80013
rs567391867	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15858133	ACCAGTAACAGGACC[C/G]CTCTGATTCAGAGGC	80013
rs567392780	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15832980	ACTGTGGTTACTTAA[A/T]GTAAGTTAAATGAAT	80013
rs567421421	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15802025	ATTATAATTTTAACA[C/T]ATTCTTTTCTCCGGC	80013
rs567439679	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15832813	CTACACATTTCTGAA[C/T]TTGAGAAAAATTCAA	80013
rs567470641	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15828435	GGAAGTATAAGGAGG[A/G]CAGGCTTTCTTTTTA	80013
rs567510764	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15787589	AAAGGAGTTAAAGCT[A/C]TTCTTGTGAGGGTAA	80013
rs567577030	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15820380	GGGATACACAGGAAA[C/T]ATTTCCAAATATAAA	80013
rs567580698	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15833194	TAATTTAAAAGTCTC[A/G]GTATTAAATTTGCTC	80013
rs567617971	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15807382	AATGGTGGAAGGTTG[A/G]ACCAGGAATGCTGAG	80013
rs567639713	snp	G/T	0.000798403	0.0199641	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15862445	GAAGTGTTTCCACAT[G/T]TGACTTTCTCCATTA	80013
rs567653140	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15814657	AATAAAAAGGTGGGC[A/G]AGAGACAGCCCCTGC	80013
rs567671936	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15846617	ATCAACCATAATTTT[A/T]CTTCCTCTACAGAAA	80013
rs567673975	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15839574	AAGAGTAGACATAAA[C/G]ATAATAATTTAGAGA	80013
rs567697095	snp	C/T			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15780081	ATAAAATTATTTTTA[C/T]ACATTCACTGGCTGA	80013
rs567713792	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15850215	ATCTTCGTAAGCTGA[A/G]CATGTATGTCGCCTC	80013
rs567752158	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15808337	GTAACTAAACTGCAA[G/T]AAAACACAAAATGCC	80013
rs567835949	snp	A/G	0.00199481	0.0315187	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15783172	GACAGGGGATGGGAG[A/G]TGGAGACCTCCCAGT	80013
rs567839475	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15821560	GTACTGAACCATAGT[A/G]CTGTGCTCAAATGTG	80013
rs567839486	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15815332	CTTTCCGTGCTTGAG[A/G]AAAGGCAATTATGTA	80013
rs567846401	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15838475	GAATATAACTAAAAT[C/T]GATATAATACTGAGA	80013
rs567868730	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15844284	CGCTTCTGATTTTTC[C/T]GCAAAAGGGCAACAA	80013
rs567904010	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15827056	GCCCATTTAGAGGCT[A/G]CAGTGAGCTATGACT	80013
rs567976717	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15780385	GAAACTACAACTCGG[A/G]CTTTTCAGTCCCCAA	80013
rs567979890	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15826509	ATAATTTCCTCAAAA[C/T]AACCTACAAATATAA	80013
rs568017500	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15818038	AGGAACAAAGAAAGA[A/G]GGAAAGATAAAATCA	80013
rs568084096	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15786463	TCAGTCTCATATCTG[C/T]GCATTAGGACATTGT	80013
rs568091556	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15831869	CTAGTAGAGACGGGG[A/T]TTCACTGTGTTGGCC	80013
rs568136531	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15819852	AGAATACACAGCAGC[A/G]ATTGACTTCCCACTA	80013
rs568174016	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15793055	TTTTCCTGGTATCCA[A/G]AGGCACTAGAGAATT	80013
rs568200861	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15792998	CTGAGGTAGGAACTC[A/G]TCCAACATCACACAG	80013
rs568224056	snp	A/C	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15813577	CGCCTCCATTAAGAA[A/C]AGACCCATATCTATT	80013
rs568231905	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15806408	TTAATCTTGGGAGGC[C/T]TGGATTAGTATGAAC	80013
rs568246770	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15849320	AAAGGGTAGTACGGG[A/G]GTAGGATGGAGGTGC	80013
rs568309859	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15805933	TGTGGTGTGCTCCAG[C/T]ACAGCCAAAAAGAGG	80013
rs568349609	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15858637	CTAAATCACATGAAC[C/T]TGAACCAAGTACATC	80013
rs568389672	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15814369	GAAGCATCACAATGA[A/G]TCGTGTAAAATATTC	80013
rs568426070	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15798393	TTCTCTGGCATTAAG[A/G]AGCTGACAGTTCAGG	80013
rs568427522	snp	C/G	0.000798403	0.0199641	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15861126	GTGTGGGCAACACCT[C/G]GACTAAAGTTTAGGT	80013
rs568450771	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15796487	GCATGAAAAAAAAAA[A/C]CAAAAAACAAAACAA	80013
rs568500189	snp	A/C	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15804369	CATAAACCTTTTAAA[A/C]TGTTGTAACATTAGC	80013
rs568543761	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15830576	CATGGGAGTTCATCT[A/T]CTTTAAATTCCACAG	80013
rs568559063	snp	C/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15791083	AAGCACAGATATTCT[C/G]AAGTGTAACCATAAC	80013
rs568559860	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15860713	TGTTTCTAAACTCCA[A/G]GAATACCTTCTTCCT	80013
rs568562097	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15785036	TAGACCACATTGCTG[C/G]ACCCACCCTTAAAGT	80013
rs568596187	snp	G/T	0.000399281	0.0141238	downstream-variant-500B	FAM188A	GRCh38.p7	10:15778000	GTTCTCATGCTTCTG[G/T]CTGGCTGAGTTAGCA	80013
rs568699032	snp	C/G			upstream-variant-2KB	FAM188A	GRCh38.p7	10:15860639	GCTTCTGACCTTTCT[C/G]AACTGTCTGGGACCC	80013
rs568714285	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15839008	AAAAATCCTCTCAAG[A/G]GTACATAGGATTAAA	80013
rs568732482	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15835639	AGAAGAAACAGAGGA[A/G]GTATCAAACGTTTTG	80013
rs568746598	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15790631	AGGTTTCTGTGTTTA[C/T]AGGCTATATCCATTT	80013
rs568771663	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15829868	ACAGGTAAGAAAACC[A/G]AGGCTCAGATAATTT	80013
rs568832819	snp	A/G			upstream-variant-2KB	FAM188A	GRCh38.p7	10:15860946	AATCAAAGTCAGACC[A/G]ACTATTACCTAAAAA	80013
rs568841708	snp	C/T	0.00795532	0.062565	intron-variant	FAM188A	GRCh38.p7	10:15848293	ACTCTTTAAATACCA[C/T]ATCATTCTATCATTT	80013
rs568895234	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15811654	TAAGAAAATGTCAAT[C/T]TGTGCTTCATCTTAC	80013
rs568908447	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15812258	TTCTTGATTTATTCT[A/G]TAAATTTCAATGTTC	80013
rs568991780	in-del	-/CT	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15823071	TAGTAAGAATATTAA[-/CT]CTGTTATTTTTGTGG	80013
rs568994934	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15859386	ATGTTTTAACCTCAT[A/C]ATCATCTTTCCTAAG	80013
rs569001520	in-del	-/T	0.00358779	0.0422022	intron-variant	FAM188A	GRCh38.p7	10:15859088	TACCTTTACAACTAA[-/T]TTTTTTCGCCTGCAA	80013
rs569036744	snp	A/G			upstream-variant-2KB	FAM188A	GRCh38.p7	10:15860900	GGGCGCTTCTCATAA[A/G]CTGGAGGCTGTCCGC	80013
rs569054116	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15818176	CAACTAAATAGTACA[G/T]AGCTAGAATTAGGAC	80013
rs569063374	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15851838	AATTAAAATAAAACC[A/C]AAACTCCTTTCTGTG	80013
rs569079521	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15846785	CTGGAGTACAGTGGC[A/G]CAATCTCGGCTCACT	80013
rs569098752	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15859054	TTCTATCGATTTGTG[C/G]AACTTTGGCCCAGTC	80013
rs569124333	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15841718	TTTTAAAAATGGGGG[A/G]AAAATCTCTAAATAG	80013
rs569151140	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15847087	TATATTTTCAAAACA[C/T]GATGGTTAAAACATA	80013
rs569168382	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15829546	ACATAGGGTTGAGTA[C/T]GAACACAGAGGCTCT	80013
rs569204281	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15830895	GGTCGTTACACATCA[C/T]GATTTTTGTTTTAGG	80013
rs569270920	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15797070	ATGTTAACATCTAAA[C/T]TGCTGTTCCCCTGTG	80013
rs569314951	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15841171	GCTCAAAAGAGATTA[C/T]TATCAAGCAGAAGTT	80013
rs569330172	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15822402	AGGCTTATAAAAGTG[A/G]TAACAGGGAGTTGAA	80013
rs569337086	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15793071	AGGCACTAGAGAATT[A/G]TTGTTGTCCAGTATC	80013
rs569344708	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15802928	AAAAAGATGTGTTTA[C/T]ACTAGAGGATGAAAA	80013
rs569444377	in-del	-/ATTATGTTTG	0.00199481	0.0315187	intron-variant	FAM188A	GRCh38.p7	10:15788493	TTGCTGAACTCTTTC[-/ATTATGTTTG]ATAAGCTCAAGTTTT	80013
rs569460032	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15802158	AATTTTTGAGGGAGT[C/G]AAAAGTTGTATGTGG	80013
rs569466434	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15858437	CCAAAGAGTGAATTT[A/G]GCATAGTCTACAATT	80013
rs569491423	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15816416	TTGACTTTAATACCA[C/T]TGAATTATTAATAGA	80013
rs569583988	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15800820	GCCATACAAACCTTC[C/T]GCTTTTTGCAAAATA	80013
rs569584306	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15808252	TCCCTATTTCCTTTC[C/T]GTATTAGATGAGGCA	80013
rs569584365	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15809440	AGGTTCGCATGTTTT[C/T]AAGTAACCTCAATGA	80013
rs569623476	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15801258	GACAGAAAGGAAAAG[C/G]CTACTGTTTTATGCA	80013
rs569647078	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15833142	ACAGGAAAGAAATAA[C/T]TGAGACCAGAAATGG	80013
rs569651234	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15812001	GGTTGGAGTGAAGTG[A/G]CACAATCTCAGCTCA	80013
rs569661498	snp	A/G	0.00478085	0.0486577	intron-variant	FAM188A	GRCh38.p7	10:15848417	AGGCGGGCGGATCAC[A/G]AGGTCAGGAGATCGA	80013
rs569680058	snp	C/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15858082	AGCAATGGCCTCAAA[C/G]AACAAACAAATGAAT	80013
rs569800017	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15839454	GAGGGGAAAACACTT[C/T]ACATTAAAACTTTCA	80013
rs569830016	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15838861	GAAAGCATTTTAATC[A/G]GAGGTAATGTTTATT	80013
rs569861864	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15793901	TTATGCTCCAAACGA[C/T]CAGTACTAAATCACT	80013
rs569910069	snp	G/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15779513	TACTGCTTTAATACT[G/T]AGGTTCTCAGATGCT	80013
rs569943923	snp	A/G	0.00279162	0.0372561	intron-variant	FAM188A	GRCh38.p7	10:15846075	TGATCTACCTGCCTC[A/G]GCCTCCCAAAGTGCT	80013
rs570096974	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15821035	GCAAGTCAATAATGG[C/T]TTAAATTCCATTTAA	80013
rs570106896	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15795355	GAGGAAAAGAGCAGA[C/T]CACTAAGTGTACAAA	80013
rs570144840	snp	C/T	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15785295	ACAACCAAATGGAAA[C/T]GTCTGTTACAGGCGA	80013
rs570150447	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15856421	CCTGGGGAAAAAGAA[A/C]AAAAAAACCCACCCA	80013
rs570159438	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15854998	CAGAGGCAAAATTAA[A/G]ATCTGCTAAACTTTT	80013
rs570179217	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15820588	TTACACAATTAAAGT[C/T]ACCGAAGATAAAAGT	80013
rs570180966	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15815239	TCTCTCTACTTCAGG[A/G]AGGAAATAAATAGCA	80013
rs570286085	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15826937	AGCCCACAAAAGCAT[G/T]TTTGGAAAATACTAG	80013
rs570298301	snp	C/G	0.00119737	0.0244387	utr-variant-3-prime, nc-transcript-variant	FAM188A	GRCh38.p7	10:15778251	AATGTAATAACAGAT[C/G]TTCTCATGCATTTAT	80013
rs570347604	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15792307	AGATCCCCAGGGCCT[A/C]GCACAGTGGTTGACT	80013
rs570355389	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15849282	ACAGAATGTTTATAA[A/G]TCAGAGAAAATTTAA	80013
rs570360492	snp	A/G	0.00318978	0.0398085	intron-variant	FAM188A	GRCh38.p7	10:15831769	CAACCTCCGCCTCCC[A/G]GGTTCAAGCAATTCT	80013
rs570423865	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15852021	GCTACTCTCCATATA[A/G]ATAAATCCTTATTTT	80013
rs570431287	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15853866	CAAGGAAAATAGCCA[C/G]TGATAAAATTTCGAG	80013
rs570432837	snp	A/G	0.0023933	0.0345097	intron-variant	FAM188A	GRCh38.p7	10:15844137	AAGTTTGCAGCGAAG[A/G]TTATATGAGAAAATC	80013
rs570457092	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15799575	TTTTACAGATTTTAC[A/G]AAGAATATATTTTGG	80013
rs570458240	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15793023	ACACAGCTAGTGAGG[C/T]GTAACGGATGGAGCC	80013
rs570481516	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15804986	GGGTAGGAAACACAG[C/T]AGACAGCCCTCTGAC	80013
rs570499213	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15798512	GTTGGGCACGGTGTG[C/T]CACGCCTGTAATCCC	80013
rs570507535	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15812592	CTAAGCAGTTTCTAC[A/G]TGGTGCATCAGTCTA	80013
rs570536998	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15824859	TGATCAGTAAACACA[C/T]GCTTAGACATCTAGT	80013
rs570571151	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15798944	CTTAGGCAAAAATCT[C/T]GGTGGACTCTAGTTA	80013
rs570593528	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15802378	TATAATCATGCCAGA[A/C]AGCGAAGGAGAAGCA	80013
rs570610385	snp	A/T	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15813510	AGCACTCATCACACT[A/T]GTAAATTTATGTGAT	80013
rs570614904	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15819235	CTTACAAAATTAACA[A/C]AAGCTCAATGACTTC	80013
rs570622665	in-del	-/A	0.00159617	0.0282053	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15860548	TAACTCCCGCCCCTT[-/A]AGGCTGAGGGCCCGG	80013
rs570667293	snp	C/T	4.97352e-05	0.00498649	intron-variant	FAM188A	GRCh38.p7	10:15843319	TGCATTATAACCATA[C/T]ATCATATCATTCTTC	80013
rs570683390	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15834960	AATGAATATGAGCCT[G/T]TTAAGGCAACTGATT	80013
rs570713400	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15835403	AATAGATGATTAATT[A/G]ACAACCAAGATTTTT	80013
rs570732219	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15831324	GGGAAAATGTGTACT[A/C]TGTGTTATCCAGGAA	80013
rs570771361	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15819776	TGCCATTAGCAGAAG[A/C]CTTAAATCTCATTTA	80013
rs570776622	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15803748	TCTATCTTTACTTCC[A/G]AGAATCTTATTAAAT	80013
rs570781490	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15861615	GCAACAGTAGTTCTG[A/G]CTTTTTTACCCATAA	80013
rs570815329	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15804247	GGCGGGGGATGGAAG[C/T]AGGTGGACCAAGCTG	80013
rs570849024	snp	C/T	0.0130921	0.0798413	intron-variant	FAM188A	GRCh38.p7	10:15818872	GGTTTAGAGCTCCTT[C/T]TGTGGGTAAGGAAAA	80013
rs570902964	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15841702	TGATGAAAATCAAGC[A/G]TTTTAAAAATGGGGG	80013
rs570942376	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15791023	TATATATGATTAACC[A/T]CAAGCTTAAACATTT	80013
rs570949940	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15797851	ACTCCCAAACCTTAG[C/T]TGCAGATTTCTACAT	80013
rs570967236	snp	C/T			upstream-variant-2KB	FAM188A	GRCh38.p7	10:15861812	ATTTTTTCCTATTTA[C/T]ACGTTATTTCTAATT	80013
rs570989878	snp	G/T	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15783887	AATTTATATTCCCTA[G/T]TTCCAGTAATTAACT	80013
rs571103541	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15841932	TTTAAGCCAAGAGGT[G/T]TCCTCTACTGAAGAA	80013
rs571129166	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15797299	TGTATTACAGTAAAA[A/G]GTAAAGCAACTTAAA	80013
rs571135878	snp	G/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15848172	CAATTTTGCACCCAG[G/T]AACTCCTCTAGGAGG	80013
rs571158706	in-del	-/ATAG	0.00199481	0.0315187	intron-variant	FAM188A	GRCh38.p7	10:15791505	TGGTAAATTAACTAC[-/ATAG]ATATCAACACAAAAG	80013
rs571212256	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15852646	AAGATATAAATTAAA[A/G]TACTAGATTAATCAT	80013
rs571215329	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15823445	CATATATGAAGATCC[A/G]GCTGTCTACTAATAA	80013
rs571281001	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15817233	TAAAATGACCACTTC[G/T]TAGAATTTCAGCATG	80013
rs571302093	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15818112	TCCTTCAATTTATAC[A/G]TAAGGAACCAGAGAA	80013
rs571339721	in-del	-/A			intron-variant	FAM188A	GRCh38.p7	10:15802810	TGTGTCTTGAACAAT[-/A]AAAAAAAAAAAAATC	80013
rs571391502	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15797055	TTTTATGGGGTACAA[A/G]TGTTAACATCTAAAC	80013
rs571459392	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	FAM188A	GRCh38.p7	10:15857958	TGTCAACTGAAGACA[C/T]GATCACAGACTATGA	80013
rs571505414	in-del	-/TCTT	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15802701	TATTTAAACAGAAAC[-/TCTT]TCTTTCTTTCCTCCC	80013
rs571537776	in-del	-/TAAG	0.00398564	0.0444627	intron-variant	FAM188A	GRCh38.p7	10:15841339	ATGTTATGAAAATTT[-/TAAG]TAATTTTTTCTTCAA	80013
rs571545499	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15851222	TTTTAGGATCTATGC[A/T]CCTTTCATTCTATAT	80013
rs571547975	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15788315	TCTAACTATTGAGAA[A/T]GGATGAAATCACAGC	80013
rs571552473	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15841019	AGAAATGTCCCCATC[C/T]TTGCTCTGGGAAGCA	80013
rs571565330	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15828553	GGGTGACATGCATAC[A/G]TGAGTATCTCAATAA	80013
rs571579755	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15796287	AAGACTTTGAGTTAC[A/T]TTTGTATCATAGATG	80013
rs571580207	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15840478	AAGACACTGACAACA[C/T]AGAGGCATTTTAGTC	80013
rs571680070	snp	A/G	0.0023933	0.0345097	intron-variant	FAM188A	GRCh38.p7	10:15833303	TGCTCCATTTTAAGC[A/G]AAGAGTGCAGTAATA	80013
rs571693241	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15846670	TTATTATGCTCTATA[C/T]AGAGCATAAGTTCTG	80013
rs571733478	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15856626	GCAGCCACACCCATA[C/T]TAACCATGGCTGCTT	80013
rs571736864	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15809369	TTCAAAAAGTTTAAG[C/T]TCTGTATTCCTTAAG	80013
rs571736915	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15853427	CTATGGTGTAATACA[C/T]TGCTGGTTCCTTAGC	80013
rs571737089	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15817724	ATTTGCTGCATTTTC[C/G]TTTTTCTTACAGACT	80013
rs571857379	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15847718	CATTTTTATTTTGGA[C/T]ATTTATTGTAATTTA	80013
rs571870610	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15806318	AGGAATCTCCACATA[C/T]GCAGACTTCATGTTT	80013
rs571884018	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15831618	TAATTGACTAATATA[A/T]TCTGTACAGGAAGTA	80013
rs571887292	in-del	-/A	0.00318978	0.0398085	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15784847	GCATTTTGTGGCTAC[-/A]GGGGAAAGGGGACAT	80013
rs571922712	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15831901	GGCTGGTCTCGAACT[C/T]CTCACCTCAGGTGAT	80013
rs571976958	snp	C/T	0.00279162	0.0372561	intron-variant	FAM188A	GRCh38.p7	10:15850035	AAATCGTGAAGATTT[C/T]ATGGACATTTATCAG	80013
rs572010230	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15815870	TTAAAACCAAAGTCG[C/T]CTGAGGCCAAAGCTC	80013
rs572102641	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15842468	TCTCAAATAGTTTCT[C/T]CTCTACTAAAATTTG	80013
rs572105969	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15826571	AAAACTGGAACTTGA[A/G]GAGCTGGGAGGAAAG	80013
rs572139616	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15779742	ATGGAGAAAAAAATT[A/G]AAAAGGATGTCAGGA	80013
rs572141650	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15820665	GGCAGGACAAATCCA[A/G]TTTGATTATCATATG	80013
rs572158567	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15826004	AACAATATGGACAAA[A/C]ATAATGTACAAATAC	80013
rs572175815	snp	A/G	0.00279162	0.0372561	intron-variant	FAM188A	GRCh38.p7	10:15803178	TAATCAGAAAGTTAT[A/G]AAACCACCTTCTATT	80013
rs572262055	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15785471	TATCAAAAGTTCCGA[C/T]AGCAGCCTTGAAATA	80013
rs572303550	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15843704	TCTGTGACACAAGAT[G/T]AACACTATTAGAGTC	80013
rs572321355	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15812776	AAATTGCTTTAATAA[C/T]AAGCAGTTACATTCA	80013
rs572328257	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15798700	CAGGAAAATCATTTG[A/T]ACCTGTGAGGCGGAG	80013
rs572338502	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15791706	AAGTGTCAAGTCCTT[A/G]GAGATTGTGGGGAGG	80013
rs572357851	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15849345	AGGTGCCAGCAAATG[A/G]GCGGCAGGAAAGATG	80013
rs572390953	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15798314	TTGGGAAATTATCGC[C/T]GTTTACATAGTAGAG	80013
rs572441608	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15844256	CATAAAGTCTACAAA[C/T]ATGCTAATCAAGCGC	80013
rs572464678	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15783591	AACTTAACCTTTATC[A/G]TAACAATTGTCTAAA	80013
rs572489075	snp	A/C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15805305	TAATGAATTACTTAT[A/C/T]CCCAGCCAACTCACT	80013
rs572597423	snp	A/G			upstream-variant-2KB	FAM188A	GRCh38.p7	10:15862406	ATGTACATAGAGCTC[A/G]TAACTGGCAGACTTC	80013
rs572598589	snp	A/T	0.000798403	0.0199641	downstream-variant-500B	FAM188A	GRCh38.p7	10:15778066	TCGAGGTCCTGTATG[A/T]CTTAGCCATTTGTAG	80013
rs572607640	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15790136	CCATGGAGAACAAGA[C/T]GTCCAAAAGCCCTGC	80013
rs572665191	snp	C/G	0.00279162	0.0372561	intron-variant	FAM188A	GRCh38.p7	10:15853562	CTGCAGTCAAAATTA[C/G]TAATTTTATTGTATC	80013
rs572669437	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15860744	CTACGCACTGCTCTG[A/G]GCTAAGCTGGAGGCT	80013
rs572724951	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15825226	TTTCAGATTAGGGAT[A/G]CTAAACTGGTGAGGA	80013
rs572751197	snp	C/G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15830316	CAGTGCTCAAGGACT[C/G/T]GATGAATATCTCTTT	80013
rs572772007	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15829885	GGCTCAGATAATTTA[A/G]CAGTTTGCCCACCGT	80013
rs572782926	snp	A/G	4.24583e-05	0.00460732	intron-variant	FAM188A	GRCh38.p7	10:15860196	AAGTGTGAGAGCCCC[A/G]CCAGGGTACCTTGCG	80013
rs572850582	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15835739	ACCATCACAGCTACT[A/C]CGAACATCTACACAA	80013
rs572861730	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15793007	GAACTCGTCCAACAT[C/G]ACACAGCTAGTGAGG	80013
rs572932170	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15803980	ACTCTTTTAGGTACC[C/T]TCAGTAGGAAGAGAT	80013
rs572971946	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15830143	TGGCAAGCTGCATAA[C/G]CAATGTCTGCCCTCA	80013
rs573039235	snp	A/C	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15849933	TACTTAACCCTCACT[A/C]ATCTGGTTTTCAACC	80013
rs573069733	snp	A/T	0.00318978	0.0398085	intron-variant	FAM188A	GRCh38.p7	10:15852824	ATTCAACCAAACACA[A/T]ATGGAAAATATTTGA	80013
rs573105789	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15847445	TTTTCAAATTTGAAA[A/C]AGTTATAAGCCAGAA	80013
rs573116151	snp	G/T			upstream-variant-2KB	FAM188A	GRCh38.p7	10:15861216	AAAAAAAGAGGGCTT[G/T]TATTGCCCGAGCTTT	80013
rs573130303	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15810837	TATTAAAAAACTCTT[A/G]TAACTCAATAACAAA	80013
rs573175327	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15831573	AGGAACAAAAACGAC[A/G]TATGTGTACATCTCA	80013
rs573186244	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15840651	AGAATAAGTCACTTA[C/T]TTAACATAAGCACTT	80013
rs573217585	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15852256	TACTGTGGCTATTGC[C/T]CAATTAATGCTTGTT	80013
rs573218189	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15811774	ATTACTAGGGTCTAA[C/T]ACATGAAGCTTTCAT	80013
rs573246141	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15829183	GAGAAAACTTTTCCT[A/G]CTGTCGGGGTTAAGT	80013
rs573281994	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15823266	AATGGTTCTTCAATT[A/G]TGGTTTAGGATTCCT	80013
rs573287842	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15817475	AGTATGAACAGTCTC[C/T]TTAAAATGTATAAAA	80013
rs573292476	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15782787	TATAATGCTTAAGGC[A/G]ATTTCAGTAATATTC	80013
rs573350339	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15839872	AACTGGAAAAATTAC[C/T]AAAATGTTTTCTGGA	80013
rs573393713	in-del	-/T	0.0228947	0.104514	intron-variant	FAM188A	GRCh38.p7	10:15841345	GAAAATTTTAAGTAA[-/T]TTTTTTCTTCAAAAT	80013
rs573407794	snp	A/G	0.00279162	0.0372561	intron-variant, downstream-variant-500B	FAM188A	GRCh38.p7	10:15782348	GGGGACTCATTTGAC[A/G]AAAGAAGGAACTTAG	80013
rs573489163	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15788447	AAGACCAAATTCTAA[A/C]AACGGTGTCTACCAA	80013
rs573517866	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15851413	ACCCTTTGCCATTCT[C/G]CCTTTTAGATTCTGG	80013
rs573542171	snp	A/C	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15795208	CATAACGCCTCTAAG[A/C]ACTAGTTACAGTTGT	80013
rs573544206	snp	C/G			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15784478	GGCCTCGTGAGGTGG[C/G]TCATACCTGTAATCC	80013
rs573557525	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15801698	ACAGCAAGAACAACA[C/T]GGAAGTCTGGTAGGA	80013
rs573569418	in-del	-/A	0.499809	0.00978247	intron-variant	FAM188A	GRCh38.p7	10:15827177	TGATATAACAGGAGT[-/A]AAAAAAAAAAAAAAA	80013
rs573597921	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15852350	AATGTGAGATAACCA[C/T]TTGGCAACTTTTAGA	80013
rs573604235	snp	C/T	0.00199481	0.0315187	intron-variant	FAM188A	GRCh38.p7	10:15846844	TTCTCCTGTCTCAGC[C/T]TCCCAAGTAGCTGGG	80013
rs573624116	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15821407	GGCTTTTTTGAATTA[G/T]TTTGTACTGGGTTCT	80013
rs573637349	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15850807	ATCTCAGCTAATAAA[A/C]ACTTGCTGGTTTTGC	80013
rs573670264	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15831581	AAACGACATATGTGT[A/G]CATCTCAAGAACCGA	80013
rs573685891	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15793996	CGCCTATTTAATTAG[A/G]AATATACCCACAGCA	80013
rs573763421	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15800101	TTTTTCTTGGAAGAA[A/T]TTTTTCTTGGAAATT	80013
rs573859255	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15793708	TCTGGAGAAGTGACT[C/T]AAACCATCAAAAGGT	80013
rs573868806	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15827270	AAGCCAGCCAGGCGC[A/G]GTAGCTCACGCCTGT	80013
rs573880353	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15827801	ACAAACACGTGAAGA[A/G]ATGATCAAGCTCAGG	80013
rs573915858	snp	A/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15780841	TATACTACATACAGG[A/T]AGAGTGGCCAAGCAG	80013
rs573980437	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15832425	AAAACCCTGTATATT[A/G]CCCAAGAGACACTGA	80013
rs574004993	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15786765	AAAACACTAAGAGCT[A/G]TTCTTTTTAGAACCT	80013
rs574090210	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15861480	TTTCATATATTGTAA[C/G]GAATAAATGGAAAAA	80013
rs574128248	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15847606	GAAGTCAAGAAACTT[C/T]CTAATTTTCTGAAAG	80013
rs574129262	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15862082	ACCTTATGTGTAACT[G/T]GCTTATGACAATTCC	80013
rs574139338	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15849967	GAGTGAATGTTGCGG[G/T]AAGTTAGGGACCCTG	80013
rs574155319	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15807088	ACATGCAGATGAAAA[C/T]GGCACGCAGCTCACA	80013
rs574179387	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15835240	GCACTCAACTCCCAA[A/G]AGTTCTACATACTGG	80013
rs574207961	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15813987	AAAACTCAAAAAAAA[A/G]AAAAAAAGAAAAAGA	80013
rs574274875	snp	G/T	0.0126979	0.078662	intron-variant	FAM188A	GRCh38.p7	10:15849446	AATATCATCTTACTG[G/T]TTTTTTTTTTTTTTC	80013
rs574322285	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15809447	CATGTTTTCAAGTAA[C/T]CTCAATGAAAGTGCC	80013
rs574331764	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15845225	TGGGATTTATGGAAG[C/T]TTATTTTATTTCACC	80013
rs574339982	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15820607	GAAGATAAAAGTCAC[C/T]GAAAATACTGTTTAA	80013
rs574386220	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15855298	AATGAAAATTAAGTA[C/T]TCTATCCTAAAACAG	80013
rs574424289	in-del	-/A	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15831207	TGTGCAGTCAGCAGT[-/A]AGAGTTTAAATGAGT	80013
rs574425027	snp	C/T	0	0	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15784833	TGTTGAGTCACTATG[C/T]ATTTTGTGGCTACAG	80013
rs574465338	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15831580	AAAACGACATATGTG[C/T]ACATCTCAAGAACCG	80013
rs574486092	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	FAM188A	GRCh38.p7	10:15778329	AAATTTGGAAAAGTG[C/T]ATTTGGCAATTACAC	80013
rs574487539	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15785348	TTTTTACCTAAAAAA[C/T]TACTACAAGTAACTG	80013
rs574503495	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15820279	CTGGAGAGGGCTCGG[C/T]GTGTCTGGGAAAGTG	80013
rs574518741	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15836475	AATACAGACATAGTC[A/C]CTAGCATAGAGTCAA	80013
rs574541565	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15842863	AACATGCAGGAATAT[A/G]ATGATAATTCTGAGG	80013
rs574545820	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15818915	AGATTGGGGTAATGG[C/T]TGCATTGCATCGTGA	80013
rs574596984	snp	C/T	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15799276	GTGATCTTGCCTCAC[C/T]GCAACCTCCACCTCC	80013
rs574603597	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15852397	GTGTAGTTCAGGGCA[A/G]GACTTAGGATTAGAG	80013
rs574608583	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15839914	TATAATATGCCCATC[G/T]AAATTAGTTACTGAA	80013
rs574671220	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15791476	TAAAAGAAAAAAATA[G/T]AACTTGCATACACTG	80013
rs574709735	snp	C/G	0.00123237	0.0247924	intron-variant	FAM188A	GRCh38.p7	10:15821615	CACAATAGTGGACAT[C/G]TAAACAAAAAACATT	80013
rs574711185	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15824310	TTTTAACAGCCATTC[C/T]GACTGGGGTAAGATG	80013
rs574853100	snp	A/G			intron-variant, downstream-variant-500B	FAM188A	GRCh38.p7	10:15782349	GGGACTCATTTGACA[A/G]AAGAAGGAACTTAGG	80013
rs574859631	snp	A/G	0.00795532	0.062565	intron-variant	FAM188A	GRCh38.p7	10:15853481	GCTGTCCTAGTGGTC[A/G]CTGTCCTAAAAAACA	80013
rs574965887	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15860132	GCGAGGGGCTGGAGC[A/G]AGAGGCGTCACAGGC	80013
rs574993278	snp	G/T			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15784715	GCACTCCAGCCTGGG[G/T]AAAGGAGCGAAACTC	80013
rs575068222	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15859766	TTTTTGGAATTAGCC[A/G]CTTGGACTTTCCCTT	80013
rs575069546	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15783483	TCTTCTCTAAAATGC[C/T]CTCCTCTCCTTCCTT	80013
rs575071411	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15823256	CAGGTAGAGCAATGG[G/T]TCTTCAATTGTGGTT	80013
rs575136108	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15835039	ATATCGATAGAGATA[C/T]AACATTAAATAATTT	80013
rs575163208	snp	G/T	0.000873362	0.0208787	missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15789249	CTATTTAGCTTACTA[G/T]TCAGGATCTGAAACA	80013
rs575311742	in-del	-/AAAAAAAAAAAAAAG			intron-variant	FAM188A	GRCh38.p7	10:15848649	AAAAAAAAAAAAAAA[-/AAAAAAAAAAAAAAG]AAAGAAAAATTAAAT	80013
rs575408719	snp	A/G			upstream-variant-2KB	FAM188A	GRCh38.p7	10:15862334	AAATATCTAATATTC[A/G]CATGCTGATTACAAT	80013
rs575422289	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15818430	AAATAAGTGTCATCA[C/T]TTTGGACAACAGTTT	80013
rs575448984	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15816772	GATCCAAACCAAATA[C/T]GAACTTATAATACTT	80013
rs575468338	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15859913	GCGCATCTTCCGTGT[C/G]ACGCCCTGCAACCCA	80013
rs575487253	snp	G/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15851569	TCACCCTAAGATAAG[G/T]CCTGCCTGCTTCAAG	80013
rs575514623	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15846238	ACCACTACTGAAATA[C/T]ACTGTACTTTATAAA	80013
rs575535214	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15787857	TTTGTGTTTAATTCA[A/T]TTAATCCTTAGGATG	80013
rs575555337	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15847361	TTTGAAATTGTTTGA[A/G]ATCAGTTGTTACGAA	80013
rs575588976	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15850485	GAAAGAGAATGCATT[C/G]TCAGGGGGGAGGTCT	80013
rs575606177	snp	A/C	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15823218	AGTTTATACTTTGTC[A/C]CTAGCTTCTTACAGG	80013
rs575721257	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15823347	ATAATATGATGTTAA[C/T]TACCTTTTTACACTT	80013
rs575755941	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15840557	GTGTATCCCATACAA[C/T]TGAAGTGTACTTTCA	80013
rs575782780	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15795678	ATAGCTAAGCATAGG[C/T]TCCAAAGTGAATGAT	80013
rs575809993	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15808470	CCAGTTTTTAAACAC[C/T]TAAGAGAGAAAGGCT	80013
rs575830543	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15839236	TAGCTTTCCAAAGCC[C/T]AGTTGTGAGTGTTTC	80013
rs575865947	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15852017	TTCCGCTACTCTCCA[C/T]ATAGATAAATCCTTA	80013
rs575892616	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15795036	CAAAATCTTCACTAG[C/T]AAAACAAAACACAAC	80013
rs575895886	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15794265	AAGTGTTCTGAGAAC[A/G]CATGATTTGCTTACA	80013
rs575905858	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15857383	TCTTCAAACTATTTA[A/T]TGTACATGTGTAATT	80013
rs575906107	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15828372	CATCTCAAACAGGTA[A/G]ATCTATAGAGAGAAA	80013
rs575907289	snp	A/G			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15784111	AGATACCTAGTGTAT[A/G]ACCTTCAACAATCGT	80013
rs575922337	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15818053	GGGAAAGATAAAATC[A/G]CAGTTCCAGAGTGGA	80013
rs575933612	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15850527	GCTCGGGGAGTGTCT[C/T]ATACAGTTGTAGATA	80013
rs575954846	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15807683	TTCCATCAGTATTTT[A/G]TCTTTAGACAATTAT	80013
rs575969385	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15801028	TTTAGAAACTGGTTT[A/G]GCTTTAAAAATATCA	80013
rs575981576	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15803734	GAAAAACATGCTACT[C/G]TATCTTTACTTCCAA	80013
rs576010489	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15799968	AATATTGAAAACTTA[C/T]GGAAGCAGATTCCTT	80013
rs576034270	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15831650	CGACTTCACGTCAAG[A/G]GCTGCCTAAGGAGCC	80013
rs576038360	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15806363	TGCTTAAGAAGATTA[C/G]TGAAACTGTGTCTAC	80013
rs576051489	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15814903	TCAGACTCACAGCTC[A/G]TTCGACACTGTTCCT	80013
rs576058180	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15801515	TGTCCCTGGCCACCC[A/C]GAATCCCATGAGCTC	80013
rs576083723	in-del	-/AACACCTGGACTAA	0.00279162	0.0372561	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15861119	GCAGAGTGTGTGGGC[-/AACACCTGGACTAA]AGTTTAGGTTTTACT	80013
rs576089739	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15806062	CTACCCACAGGATGG[G/T]CTGTTCTCATCGCCC	80013
rs576119483	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15815460	GACTAGAGTATAATT[C/T]ATACCACTTGTACTT	80013
rs576152931	snp	A/G/T	0.000880015	0.0209579	intron-variant	FAM188A	GRCh38.p7	10:15786687	AGTGGATACCAGAGG[A/G/T]AAAAAAAAAGCTGCT	80013
rs576165355	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15820724	GAAAAAGGAACGCTG[C/T]CTGACGAAAAAGAGG	80013
rs576229932	snp	C/G	0.00119737	0.0244387	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15785564	CAGTCAGAATGTGAA[C/G]AAAGAGGATATCACA	80013
rs576257185	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15793243	TCATGTGGAACACTT[C/T]GAATAGACCTGATAA	80013
rs576257870	snp	A/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15779791	AGACGTTGAAAGATC[A/T]AACTAACCAGATACT	80013
rs576309064	in-del	-/T	0.0430285	0.140224	intron-variant	FAM188A	GRCh38.p7	10:15800226	TAGATACTAGTCTAT[-/T]TTTTTCTACTACCAT	80013
rs576344083	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15792580	ATTCTAGAGAATGCC[C/T]AGGGAGTGGTGTATA	80013
rs576359814	snp	C/G	1.93351e-05	0.00310921	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	FAM188A	GRCh38.p7	10:15778986	CCTTATAAATACTTA[C/G]ACAAATTAATTTAGT	80013
rs576425934	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15838045	ATTAAGGACTCAGCA[C/T]AGTTTATACATTTAC	80013
rs576470379	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15815298	AGTAACTCTGTACTT[C/T]TAGCATTTAATTTTA	80013
rs576668190	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15855105	CACAGGTGGGGCTTT[C/T]AGTTGGAAATGCGTT	80013
rs576705475	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15820210	AGCCTGAAGGGGACA[C/G]TGAGCCATCCATCTC	80013
rs576798978	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15860805	ATGCCCATTGCTTGT[A/G]TTTTTCAATATTAAT	80013
rs576818602	snp	C/T	0	0	intron-variant	FAM188A	GRCh38.p7	10:15852880	TCTGTACTAAACATG[C/T]ACAGACTTTCTTTTT	80013
rs576872431	in-del	-/A	0.00636936	0.0560724	intron-variant	FAM188A	GRCh38.p7	10:15800595	ATACTGTAACTCTTG[-/A]AAAAAAACCATGGAA	80013
rs576876975	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15824634	TAAATGTAAGCAACA[C/T]TAAATGTTTTCATGT	80013
rs576878963	snp	G/T	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15830881	GAGGTTTGTGGCCTG[G/T]TCGTTACACATCACG	80013
rs576934058	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15800757	ATAAATGAATCCAGC[A/C]TAAATATCGTAAAGA	80013
rs576939158	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15804227	ATGCAGAGGGTTGGC[A/G]GGGGGGCGGGGGATG	80013
rs576994572	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15829319	CGTCTGAATAGAACA[A/G]TGGTTCTTAACCCTG	80013
rs577033916	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15829681	TAACTTGTCAGTTTG[C/T]AGAATATACTGGAGT	80013
rs577070297	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15808499	CTCTAACAGTTCACC[A/G]CAGTGTTTTTCCTGT	80013
rs577105206	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15834278	TTTTCTCATTTAAAA[A/T]AATTACAAATGGATT	80013
rs577113201	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15797600	ATGTAACATCATAAA[C/T]GTGCAGTTATATTTG	80013
rs577169985	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15812461	TCTGCCTTCCTACCC[A/G]TGCAATATTAGAAAA	80013
rs577201837	snp	A/C	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15803170	CAGAGATGTAATCAG[A/C]AAGTTATGAAACCAC	80013
rs577250778	snp	C/T	0.00835141	0.0640778	intron-variant	FAM188A	GRCh38.p7	10:15827580	TAAATAAATAAAAGC[C/T]TTGGATATAAAAAAA	80013
rs577254956	snp	A/G	0.00557542	0.0525036	intron-variant	FAM188A	GRCh38.p7	10:15804623	CATATTATAGTGTTT[A/G]AAGTCCCTCCAATAA	80013
rs577262819	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15817583	GTGTGTGTGACTGAG[A/G]AAAAAAAAGTTTAAT	80013
rs577275959	snp	C/T			utr-variant-3-prime, nc-transcript-variant	FAM188A	GRCh38.p7	10:15778225	GATCATAATAAATAA[C/T]GTAATATACTAATGT	80013
rs577277201	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15809679	CCCTGCTGCTTGATG[A/T]CTCTGCAGTTCCTAT	80013
rs577287467	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15855337	TGAGTAGACTTCTCT[C/T]TTCATAATAAGGTTT	80013
rs577304550	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15818314	TTTAAATTAAGGTAG[A/G]AGTAAAAAAAAAAAA	80013
rs577342948	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15856394	TCAACTACACCTACA[C/T]GCCCCTCTTCCCCTG	80013
rs577376694	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15823296	TCAGGGACCACAAGA[C/T]CCTCTTAGAGACTAC	80013
rs577401747	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15858986	GGAACTCAAAGGAAG[A/G]TAATGAAAACAGAGG	80013
rs577435670	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15808889	GATGAAACTAGATGC[C/T]ATAGGCAGGGTCCAA	80013
rs577437380	snp	C/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15796519	CACAAAAACAAAACC[C/G]AAACCATTTTTTCCA	80013
rs577475255	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15789185	GCAAAAAATGTACAA[C/T]ATGTCTTAAACTTAA	80013
rs577498822	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15789102	AATATTGGATTAGTT[C/T]GATTTCTTAATCTTT	80013
rs577520855	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15840744	AGCAACTCTTAACTA[C/G]CTTCCGTACCACTAG	80013
rs577521698	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15847240	TTAACAGTTTATAGC[A/G]AATCAGCCTTTGAAA	80013
rs577532635	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15783273	TTCATGTATTTTCCC[C/T]CTCACTTATGCCAAT	80013
rs577552561	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15816153	GTAGTCCCAGCTACT[C/T]GGGAGGCTGAAGTGG	80013
rs577583685	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15788673	ATCTTAATCTACAGA[A/G]GAAGTTGTAGATGTA	80013
rs577605443	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15853359	TACATGATAAAACTA[A/T]GATATGATTTGCCCC	80013
rs577678461	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15794479	GTCATATATAGAGGC[A/G]TACTTTCTAAGCTAT	80013
rs577684333	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15846911	TGTATTTTTAGTAGA[C/G]ACGGGGTTTCACCAT	80013
rs577684988	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15836505	ATCAACGCTCAAAAA[A/C]CATTTGTCAAATAAA	80013
rs577721256	snp	A/G	0.00517822	0.0506191	intron-variant	FAM188A	GRCh38.p7	10:15786979	CTTTGCTTCATAGGT[A/G]TGCCTGAATTTAACA	80013
rs577822744	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15842075	GACCGTCAGCACATA[C/T]GTTACCAAAGTCCAT	80013
rs577869346	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15822013	TGAGAGAATTTACTC[A/C]CTGAAATCCATGCCA	80013
rs577894718	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15822562	ATGTTTCTGGTCTGG[C/G]GGGACATGATAAATA	80013
rs577904678	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15858216	GCCTTGAAGAGCTAC[A/G]TATCCAAAATATAAC	80013
rs577931805	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15827330	ACGGATCACCTGAGG[A/T]TGGGAGTTCGAGACC	80013
rs578002619	snp	A/G	0.00279162	0.0372561	intron-variant	FAM188A	GRCh38.p7	10:15857689	CCAAAAAAAGAAGAA[A/G]AAAAAAAACACCCCG	80013
rs578016239	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15839692	GAAAGAACAGGTAAA[A/G]TAGATTGTTACACGG	80013
rs578021615	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15794153	GTCAGTTATTCTAAA[A/C]GCATTCTGAGGAGGG	80013
rs578051152	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15832835	AAAATTCAAATGGAA[A/G]ATCATGAATCACTTC	80013
rs578077183	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15827916	AGTGTCAGGCAGGAT[A/G]CAGAAAAATACGAAC	80013
rs578106771	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15814920	TCGACACTGTTCCTT[C/G]TATTATACCTTCTGT	80013
rs578108729	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15800923	AATATGATTTAAGAA[A/C]AAGTGCAGTCATTAT	80013
rs578133789	snp	C/G	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15832475	TTGACAGGATTAAAT[C/G]CTTTCAGCTATGAAT	80013
rs578146605	snp	G/T	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15799371	GCCCGGCTAATTTTT[G/T]TATTTTTAGTAGAGA	80013
rs578220216	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15800302	GGGGCATACGGACTG[C/T]ACCTGGCACCACTCA	80013
rs578235078	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15839117	TCATAAAGCAAATCT[G/T]ACTACTATCAAATAT	80013
rs578238142	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15815422	ACATAATTACATTCA[C/T]GAAACTTAGCATTGT	80013
rs578260270	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15807419	TTTGATAAGCGTATT[C/T]TGGGCAGAGGATAAC	80013
rs745325088	snp	A/C			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15784515	TTTGGAAGGCCAGGA[A/C]GGGTGGAACACCTGA	80013
rs745344839	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15854629	TATATTGAGAGTGAG[A/G]GGAATGAGAAGGGTA	80013
rs745345143	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15857471	AAGAGCTTGGAATAC[C/T]GGTGTAGTTTGTGGG	80013
rs745374220	snp	A/G	5.10434e-05	0.00505164	intron-variant	FAM188A	GRCh38.p7	10:15786685	ACAGTGGATACCAGA[A/G]GAAAAAAAAAAGCTG	80013
rs745389552	snp	A/G	1.65493e-05	0.00287652	utr-variant-5-prime, missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15837274	ATTGAATACTGGTCC[A/G]AGACAGCATCTTTTA	80013
rs745426134	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15827927	GGATGCAGAAAAATA[C/T]GAACTCTCCTACACA	80013
rs745431247	snp	A/G			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15783775	TTGATCGTTTCCTTA[A/G]TTACAGGAGTCATTG	80013
rs745448647	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15797135	GTTGTTCTAATATCT[C/G]ACCTTTACTCTGTTC	80013
rs745458010	in-del	-/T			intron-variant	FAM188A	GRCh38.p7	10:15811246	TTGAAATGTCAAAGA[-/T]TTTTTTTTCTGAGAA	80013
rs745462593	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15817003	TATCTGAAGCATAAA[A/G]TGTCCAATTTGTATT	80013
rs745550953	snp	C/T	1.6743e-05	0.0028933	synonymous-codon, nc-transcript-variant	FAM188A	GRCh38.p7	10:15789258	TTACTATTCAGGATC[C/T]GAAACAAGGTCCAAT	80013
rs745596206	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15791743	TCAATGCAAAGGAGC[A/G]CTGATGAAGGACAGT	80013
rs745624708	in-del	-/AA			intron-variant	FAM188A	GRCh38.p7	10:15827178	GATATAACAGGAGTA[-/AA]AAAAAAAAAAAAAAA	80013
rs745640142	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15841971	AATGTAAAGGCCTGT[G/T]GAAACCTCTATTTTT	80013
rs745672219	in-del	-/AACTAA			intron-variant	FAM188A	GRCh38.p7	10:15797241	AAAAACAGGAATGGG[-/AACTAA]AACAAGGCAACCTGT	80013
rs745674120	snp	C/T	3.30879e-05	0.00406729	intron-variant	FAM188A	GRCh38.p7	10:15847834	TTTCAAAATGTCCCT[C/T]TAAGGAGTTGGTAAA	80013
rs745698436	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15833547	AGGTAATGTAGAGCC[A/C]TTAAATAGACGAATA	80013
rs745700443	in-del	-/GTG			intron-variant	FAM188A	GRCh38.p7	10:15800434	TCTCCTGATGCTATT[-/GTG]GTGAGCTTGTGTTGT	80013
rs745710199	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15847537	GTACAATTACAGTGA[C/T]TGTACCTATCTAGTG	80013
rs745720637	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15803429	TTGAGAGAGTTTTAC[A/C]ATCAAGACAAAACAC	80013
rs745807288	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15851571	ACCCTAAGATAAGGC[C/T]TGCCTGCTTCAAGGC	80013
rs745820825	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15822136	TGCTAATCACTGGTA[A/G]AATTTATCATTAGGT	80013
rs745847827	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15834274	TAAATTTTCTCATTT[A/C]AAAAAATTACAAATG	80013
rs745870397	snp	C/T	3.31824e-05	0.00407309	intron-variant	FAM188A	GRCh38.p7	10:15833611	TCAAAGAGAGCAACA[C/T]AACAAGGAATATACT	80013
rs745932748	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15849996	TGAATGGAGGGACCT[C/G]CTGAAGCTGTGACAG	80013
rs745936839	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15815915	GTGGAAAAACATGAT[A/C]TACAGATTATAGTTG	80013
rs745962105	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15800356	TAAAGATGCAGTATC[A/C]GATCACAACAGCATA	80013
rs745968898	snp	A/G	1.85139e-05	0.00304247	intron-variant	FAM188A	GRCh38.p7	10:15833733	AAATATTAAAAAGCA[A/G]TTAAATATGAATATA	80013
rs745982894	snp	A/G	1.66913e-05	0.00288883	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15779156	CCTGTTGAACAAAAT[A/G]AAGCCACCAAGGTCA	80013
rs745985428	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15843968	AATCTCTAGAGGGCA[A/G]GTCCAAGAAAAAACA	80013
rs746021770	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15848146	TGCACGTAAGAGTAC[A/G]TATACTCACACAATT	80013
rs746035679	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15832120	CTAGGGTAAGCTATC[A/G]AGAATCCGGAGAACG	80013
rs746102277	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15831228	TTAAATGAGTTTAAG[C/T]AGGATTAATTTAGAG	80013
rs746125841	in-del	-/A			intron-variant	FAM188A	GRCh38.p7	10:15815887	GAGGCCAAAGCTCTT[-/A]AACCACTCAATTGTG	80013
rs746137463	snp	A/G	1.67534e-05	0.0028942	intron-variant, utr-variant-5-prime	FAM188A	GRCh38.p7	10:15838286	CCAAGGCAGCTATAC[A/G]TAAAAGACACTTTTC	80013
rs746264268	snp	C/T	1.64904e-05	0.00287139	missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15796109	TTTTACCTTCTGGGT[C/T]GTAGGTTTGAAAAAC	80013
rs746292690	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15839392	AAAACTATACACACC[A/G]CATAAGCCAATGAAA	80013
rs746309387	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15826702	GTAATTGTGAAGTTT[C/T]GCATAAGAAGTCACA	80013
rs746396581	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15827638	GAGAAGGCTGGGTGA[C/T]AATATTTGCAACACA	80013
rs746462837	snp	A/C			intron-variant, downstream-variant-500B	FAM188A	GRCh38.p7	10:15782384	TGGAGTTGTAACTAC[A/C]AGAAAGCCCTGAAGT	80013
rs746473620	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15796027	TATATCTTTTGAATA[A/T]AATCAGGTCGCTATC	80013
rs746504810	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15831307	TCAGCCTGGCAGTGG[A/G]AGGGAAAATGTGTAC	80013
rs746512104	snp	A/G	1.66599e-05	0.00288611	synonymous-codon, nc-transcript-variant	FAM188A	GRCh38.p7	10:15834614	TTTTATGTTTTCAAT[A/G]CCCTAAAGAAACAGA	80013
rs746530525	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15807853	CAAATACAGCTGCAT[A/G]AGGCAAAGAGTACAT	80013
rs746564734	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15837071	GAAACAGAAATTAAC[C/T]CATTTTCAACGTAAA	80013
rs746570743	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15795242	AAGACTGATACCTAA[A/G]AAAACAGTAGACCTA	80013
rs746602545	snp	A/G			upstream-variant-2KB	FAM188A	GRCh38.p7	10:15860842	AAACTAGAACTATAA[A/G]GCAATAGTTGAGTCA	80013
rs746655650	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15854473	TTTAAATTTTTTGAG[G/T]TGAAGTCCTCAATCA	80013
rs746693655	snp	C/T			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15783747	ATGCCTTACAGAAAA[C/T]AGAAAAATCAATTTG	80013
rs746694573	in-del	-/AAA			intron-variant	FAM188A	GRCh38.p7	10:15796476	TAAAAATGTAGCATG[-/AAA]AAAAAAAAAAACAAA	80013
rs746712630	snp	A/G	1.65345e-05	0.00287524	missense, intron-variant, nc-transcript-variant	FAM188A	GRCh38.p7	10:15786571	GTTACCTGATCAGGA[A/G]AAAATTCTTGAAGAA	80013
rs746799257	snp	A/G	1.68821e-05	0.0029053	intron-variant	FAM188A	GRCh38.p7	10:15786679	AGAAAAACAGTGGAT[A/G]CCAGAGGAAAAAAAA	80013
rs746801132	snp	A/G	3.3106e-05	0.0040684	utr-variant-5-prime, missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15841582	AGGTATGACAAAGGA[A/G]TTCCTTCTGCTCTTC	80013
rs746815849	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15845883	GCTAGAGTGCAGTGG[C/T]GTGATCTCGGCTCAC	80013
rs746842516	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15815338	GTGCTTGAGAAAAGG[C/T]AATTATGTATCTTGC	80013
rs746853972	in-del	-/AA			intron-variant	FAM188A	GRCh38.p7	10:15789563	CTCCGACGAAAGCTT[-/AA]AGTCAAATTACTTGA	80013
rs746865019	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15844981	CACCCCTGAATCTTA[C/G]TGTTTTTCTAATTAA	80013
rs746870713	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15801679	GCTATTAAAGAGAAC[C/T]GCAACAGCAAGAACA	80013
rs746921427	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15790124	AAAAAAATCTTGCCA[C/T]GGAGAACAAGATGTC	80013
rs746985108	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15846606	GATATTTTGGAATCA[A/C]CCATAATTTTTCTTC	80013
rs747029395	snp	A/G	3.32552e-05	0.00407756	intron-variant	FAM188A	GRCh38.p7	10:15833598	GAAATATTATTCATC[A/G]AAGAGAGCAACATAA	80013
rs747031404	snp	C/T	4.98674e-05	0.00499312	missense, downstream-variant-500B, nc-transcript-variant	FAM188A	GRCh38.p7	10:15779062	TTGGTTTGCAGACAG[C/T]GTTTAATAGGAGTGT	80013
rs747032462	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15812673	AAGTCATGTCAGAGA[A/G]GCTACAGCATAGCTC	80013
rs747110199	in-del	-/TTAA			intron-variant	FAM188A	GRCh38.p7	10:15811880	TTTCTAATTAGATGC[-/TTAA]TTCAGTTTTCCATGT	80013
rs747121558	snp	C/T	1.66255e-05	0.00288314	synonymous-codon, nc-transcript-variant, intron-variant	FAM188A	GRCh38.p7	10:15821707	TCCTACTGCTGCTTG[C/T]TCATGTATACCAAGA	80013
rs747145893	snp	C/T			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15780579	GGCTCGGATGCCTGG[C/T]GGCTCAGACTCCATC	80013
rs747149300	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15811227	AATTCACAATAAAAC[C/T]GAAGTTGAAATGTCA	80013
rs747150442	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15841660	AAAAAAATTCTGTCA[C/T]GAATAACAATAGTAA	80013
rs747166531	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15830068	CATGACAGTAAGGTA[C/T]AAATAACTAGCAGGT	80013
rs747187032	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15843826	AGTCAACGATGTTAC[A/G]TTGGTTATTTGATAA	80013
rs747201374	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15853145	ATGATAGTTTGAAGG[C/G]TAGTTGGATCAAGAA	80013
rs747208572	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15800155	AACTGTGCAGCCTAG[A/G]GATATTTTCAAAAGT	80013
rs747295128	snp	A/G	3.32984e-05	0.00408021	intron-variant, downstream-variant-500B	FAM188A	GRCh38.p7	10:15779144	CTACGTACATGACCT[A/G]TTGAACAAAATAAAG	80013
rs747337200	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15803773	TTAAATTTATCCTAA[A/G]AAAATTATCTTCCAA	80013
rs747403863	snp	A/T	0.000115467	0.00759737	intron-variant	FAM188A	GRCh38.p7	10:15837534	TATCATTAAGAAAGA[A/T]CACCTACTTGGCAGG	80013
rs747411537	in-del	-/GAGT	1.74644e-05	0.00295497	intron-variant	FAM188A	GRCh38.p7	10:15838194	GGCAATGTGTCCACA[-/GAGT]AAGTATTTTAAATGT	80013
rs747428000	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15818440	CATCACTTTGGACAA[C/T]AGTTTGACACTTCCT	80013
rs747488265	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15859583	GGTTACAAGCATACC[C/G]GCCGAGGAAGTACTA	80013
rs747497697	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15802052	CGGCTTACGAGATTA[C/T]AGTATATAATACATA	80013
rs747508743	snp	A/C	1.65042e-05	0.0028726	intron-variant	FAM188A	GRCh38.p7	10:15796069	AACATATGAAGACAT[A/C]AAACACAGAGATGAT	80013
rs747517312	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15849300	AGAGAAAATTTAACA[C/T]AGCTAAAGGGTAGTA	80013
rs747653222	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15836775	GAGGTAACAGATAAA[C/G]AAGGAAACAAAGCTA	80013
rs747671156	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15806789	ATTACTATTCCCCAA[A/G]CACAGTATTAACTTT	80013
rs747678695	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15805366	TAGAAGGATAGTTAA[C/T]GTTACATTTTAAAAG	80013
rs747691404	snp	A/G	0.000115969	0.00761387	intron-variant	FAM188A	GRCh38.p7	10:15860161	GCGGACTCTCGCAGG[A/G]CAAAAGAAGCAGCGG	80013
rs747704806	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15848527	TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCCGA	80013
rs747711854	snp	A/G	1.65696e-05	0.00287828	intron-variant	FAM188A	GRCh38.p7	10:15796216	CAGCTACAGTATTAT[A/G]ACATTAAAAAGAAAA	80013
rs747742631	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15833983	AAAATGACAGACTAA[C/T]AAGTTACTTAATATT	80013
rs747772506	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15794924	ATTTTTTCATGCCTT[C/T]ATTCTTTAATAGTTA	80013
rs747772616	snp	A/G			intron-variant, missense	FAM188A	GRCh38.p7	10:15780951	TCACTTGATCTCCCC[A/G]TCTCAGATGCCTCAT	80013
rs747802313	snp	C/G	2.57357e-05	0.00358709	utr-variant-5-prime, missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15860241	ATGGTGTCCGAGAGA[C/G]CGGGGCTGCTCTTGG	80013
rs747850230	snp	C/G	1.94554e-05	0.00311887	intron-variant	FAM188A	GRCh38.p7	10:15833749	TTAAATATGAATATA[C/G]TTGCCAAATCAAATA	80013
rs747893028	snp	C/G/T	0.000182056	0.00953922	intron-variant	FAM188A	GRCh38.p7	10:15786553	ATATATTTCCTCAAC[C/G/T]ATGTTACCTGATCAG	80013
rs747953002	snp	G/T			utr-variant-3-prime, nc-transcript-variant	FAM188A	GRCh38.p7	10:15778385	CAGATTCTCTTTTCT[G/T]TCAGTTTTTAGAATA	80013
rs747954176	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15826308	AAGAGTGGGCAAGAA[A/T]GCATTTAATTTGATT	80013
rs747978888	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15815116	AAAATACATTTTTGT[G/T]TGTAAGTCAGAATTA	80013
rs747984425	in-del	-/A			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15779795	TTGAAAGATCAAACT[-/A]AACCAGATACTGTAT	80013
rs747987545	snp	G/T	1.67349e-05	0.0028926	synonymous-codon, downstream-variant-500B, nc-transcript-variant	FAM188A	GRCh38.p7	10:15782182	ATTTGACTGCTTCAA[G/T]CCATTGTAGTGGTAG	80013
rs747994909	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15812916	ACCCAGTCCTGTCAT[C/T]CTACCTCAGGAGTAA	80013
rs748029394	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15801411	AGAATGCTTTCTCTG[C/G]ATCAGTTCTATCAAT	80013
rs748096161	in-del	-/TTTA			downstream-variant-500B	FAM188A	GRCh38.p7	10:15778133	AGAAGTACGTATTTG[-/TTTA]TTTATTTTGAGCCAC	80013
rs748096701	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15845492	ATTCTTTACAAAGTT[C/T]ACGTGACTCTTTTTT	80013
rs748113586	snp	C/T			utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	FAM188A	GRCh38.p7	10:15778875	AAAATGTGTTTTTAA[C/T]TGTTATTTACAGTTA	80013
rs748127000	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15854188	GTTTTAGATTTCGTA[C/T]TGCAACTAATCTCTA	80013
rs748134242	snp	A/G			upstream-variant-2KB	FAM188A	GRCh38.p7	10:15862282	ATTATCTCTCAGCAA[A/G]TGAGAGATCGGGGAA	80013
rs748204806	in-del	-/AATC	1.7351e-05	0.00294537	intron-variant	FAM188A	GRCh38.p7	10:15837169	GCACTGAACAACATT[-/AATC]AAAGGCAGAAAAATC	80013
rs748208196	snp	A/C/G			intron-variant	FAM188A	GRCh38.p7	10:15822774	GGAATCATCAGCATA[A/C/G]AGATGAGAGTTAAAG	80013
rs748211214	snp	C/T	1.6513e-05	0.00287336	intron-variant	FAM188A	GRCh38.p7	10:15843207	TTAAAAGACAGCTAT[C/T]ATACCTGAACAATCC	80013
rs748269193	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15787801	TTAATGAGTCTGAGT[A/G]AGGCCGGGAAGTTAT	80013
rs748321303	snp	C/T			downstream-variant-500B	FAM188A	GRCh38.p7	10:15778050	AGGCCTGGTCTCTTA[C/T]TCGAGGTCCTGTATG	80013
rs748330860	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15810914	GTTTATCCAAAGAAC[A/G]TCTAGAAGTGGACAA	80013
rs748357148	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15822498	ACAACAAACAGGTAT[A/G]AAAAATCGATGCATT	80013
rs748361173	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15859969	CCAGCCGAAGGGCAG[C/T]CCGGAGGATGGAAAG	80013
rs748421043	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15856390	TCAATCAACTACACC[C/T]ACACGCCCCTCTTCC	80013
rs748441646	snp	A/G	1.66106e-05	0.00288184	missense, nc-transcript-variant, intron-variant	FAM188A	GRCh38.p7	10:15821696	AGTGTTAAAAATCCT[A/G]CTGCTGCTTGTTCAT	80013
rs748452991	in-del	-/T			intron-variant	FAM188A	GRCh38.p7	10:15834538	AGAGATTTTAGTTAA[-/T]TTACCTGCCATGTCC	80013
rs748512644	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15853431	GGTGTAATACATTGC[C/T]GGTTCCTTAGCATAC	80013
rs748542130	snp	C/T	1.65707e-05	0.00287838	utr-variant-5-prime, missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15837286	TCCAAGACAGCATCT[C/T]TTAATTCTGGTAAAC	80013
rs748543157	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15818380	ATGCTAAACTCATGA[A/G]ATGTTTTGTAATAGT	80013
rs748576942	snp	G/T	1.66983e-05	0.00288944	stop-gained, downstream-variant-500B, nc-transcript-variant	FAM188A	GRCh38.p7	10:15779037	CCAGAGTAACTCAAT[G/T]TATGGCCATTTGGTT	80013
rs748592154	snp	A/G			utr-variant-5-prime, stop-gained, intron-variant, nc-transcript-variant	FAM188A	GRCh38.p7	10:15847905	GGCCACCTTCAAACT[A/G]TTCTAATGCAGATCC	80013
rs748602161	in-del	-/C	1.65436e-05	0.00287602	intron-variant	FAM188A	GRCh38.p7	10:15796204	CATGTTGTCAACCAG[-/C]TACAGTATTATGACA	80013
rs748647772	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15858526	CAGATAGTGTGCTAA[C/G]CACCTAAATTATTTA	80013
rs748653459	snp	G/T	1.70284e-05	0.00291786	intron-variant	FAM188A	GRCh38.p7	10:15837353	AAGTATTGGTATCAT[G/T]ATGAGATTAACTACA	80013
rs748722016	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15817292	GACGATAATAACTTT[A/G]TAAGGAAAATAATTA	80013
rs748778441	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15818297	TTCAGAAAAAGTGTG[C/T]ATTTAAATTAAGGTA	80013
rs748788406	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15846909	TTTGTATTTTTAGTA[C/G]AGACGGGGTTTCACC	80013
rs748828553	snp	C/T	1.66952e-05	0.00288917	synonymous-codon, nc-transcript-variant	FAM188A	GRCh38.p7	10:15789297	CACATCTTCCAGAAG[C/T]GAATCGGGTATGAAT	80013
rs748857135	snp	C/T			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15786321	CCGAACTGTTCTCTC[C/T]GTATCATTATGTGTA	80013
rs748866394	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15817160	TATAGATTTAACACA[A/G]CTGGAGATAACTATT	80013
rs748901185	snp	C/G	1.65135e-05	0.00287341	intron-variant	FAM188A	GRCh38.p7	10:15847844	TCCCTCTAAGGAGTT[C/G]GTAAAGGAGTCTATG	80013
rs748901261	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15805196	TTTCTTGAAGTTAGA[C/T]GACGTTCTTGGAGGT	80013
rs748946770	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15791894	TAAACAGGAGAGCCT[A/G]GCAGGTCTCAATTTT	80013
rs748976487	snp	C/T			intron-variant, missense	FAM188A	GRCh38.p7	10:15780891	ATCAGGAACTCAGTT[C/T]CAATCCCTGTTCTGC	80013
rs748983702	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15847729	TGGATATTTATTGTA[A/G]TTTACATGAGCAAAA	80013
rs749082044	snp	G/T	1.92298e-05	0.00310073	intron-variant	FAM188A	GRCh38.p7	10:15833745	GCAATTAAATATGAA[G/T]ATAGTTGCCAAATCA	80013
rs749102722	snp	C/T	1.65053e-05	0.0028727	missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15833657	ACTCTCTATCACCAT[C/T]CCATACATTAGAAAC	80013
rs749104066	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15793450	GCTTGATATCAAAAT[A/C]AGTACTGGGCTCCTA	80013
rs749104486	snp	C/T	1.67565e-05	0.00289447	intron-variant	FAM188A	GRCh38.p7	10:15847977	AGGAAAGATTAAAAA[C/T]ATAATTCAAGTAGCA	80013
rs749131974	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15835922	ACTCTAGTCTTATAT[G/T]ACAAACACCAACTCC	80013
rs749217435	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15811458	AGTGCTAGTCATGAG[A/G]CTATGTATAGATTAA	80013
rs749253065	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15852453	TGTCAGTTAAAGTGA[A/G]TGAGAACTTGTAAAA	80013
rs749263557	in-del	-/AGA			intron-variant	FAM188A	GRCh38.p7	10:15801976	TGAGGAAGATGACGT[-/AGA]AGAAGCAGGGCCAGA	80013
rs749288780	snp	C/T	1.69836e-05	0.00291402	missense, downstream-variant-500B, nc-transcript-variant	FAM188A	GRCh38.p7	10:15782159	AATTATCATACCTTT[C/T]CATTATAATTTGACT	80013
rs749327801	snp	A/T	1.69077e-05	0.00290751	utr-variant-5-prime, missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15841431	TATATCTTACAAGAA[A/T]GTTCCACTTGGCAAC	80013
rs749351166	snp	C/T	4.9769e-05	0.00498819	intron-variant	FAM188A	GRCh38.p7	10:15786535	CCAACAGAATAACAA[C/T]GAATATATTTCCTCA	80013
rs749373072	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15802380	TAATCATGCCAGACA[C/G]CGAAGGAGAAGCAAG	80013
rs749414857	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15808281	CACGAAATCTCAATA[C/T]ATGCACAAACTCCAG	80013
rs749421381	in-del	-/AT	1.65089e-05	0.00287301	intron-variant	FAM188A	GRCh38.p7	10:15796057	CAATGTATTTCAAAC[-/AT]ATGAAGACATAAAAC	80013
rs749433442	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15832185	TGTGAGAGAGAGTGA[C/T]GCGCTAAAGACAGTG	80013
rs749452947	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15788714	AAACATAACAGTGAG[A/C]ATGAAGACAATGACA	80013
rs749511091	in-del	-/AA	0.000116296	0.00762461	intron-variant	FAM188A	GRCh38.p7	10:15834523	TTCACATGAGGAGAC[-/AA]GAGATTTTAGTTAAT	80013
rs749516028	snp	A/T			upstream-variant-2KB	FAM188A	GRCh38.p7	10:15860986	GAATGTGGCATAATG[A/T]GCATTAGAAATGCTT	80013
rs749532357	in-del	-/TTC			intron-variant	FAM188A	GRCh38.p7	10:15831012	TGGAAAGATATATAG[-/TTC]TTCTAAAACAGGAAA	80013
rs749577806	snp	C/T	1.65236e-05	0.00287429	utr-variant-5-prime, missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15841542	CCAGAGTGGTCACAA[C/T]AAGCACTTTCTAAAA	80013
rs749605867	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15797349	ACATTTGTAAAATTT[C/T]GTAATGCACAGTTGT	80013
rs749646754	snp	C/T	1.64855e-05	0.00287097	utr-variant-5-prime, synonymous-codon, nc-transcript-variant	FAM188A	GRCh38.p7	10:15860288	CATCAGCTCTTTAGT[C/T]AGTTCGGACATGATG	80013
rs749657603	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15826868	TCCCAAACTCATACC[A/G]TTCATAAATACAAAA	80013
rs749694933	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15829015	GATCCTATTTCCAAA[A/C]TGCCTACACTGGCCC	80013
rs749695338	snp	C/T	3.31257e-05	0.00406962	splice-acceptor-variant, intron-variant	FAM188A	GRCh38.p7	10:15816916	CAAGTAAGAACCAAC[C/T]TAGAACAAATGTAGC	80013
rs749703657	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15839828	ATATGGTTTACTTCA[A/T]GGCAACTTTTAAAAT	80013
rs749736347	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15857261	CCTGGAGCACTCTTT[C/G]TTCCGACTTCTGCAT	80013
rs749763102	snp	A/G			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15784638	GCTACACAGGAGGCT[A/G]AGGCAGGAGAATTGC	80013
rs749784748	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15841138	AGCATATCATTATTT[A/C]TAAATAAGAGTTCTA	80013
rs749824281	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15828099	TTGGTCTATGGCAAA[A/G]AAACACTAAAATATA	80013
rs749912869	snp	C/T	1.82261e-05	0.00301872	intron-variant, downstream-variant-500B	FAM188A	GRCh38.p7	10:15782114	CACATAATTATTTCA[C/T]CAACCCAGTTGAACA	80013
rs749949209	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15852040	AATCCTTATTTTTCA[A/G]GTCTCAGTTTAGGTG	80013
rs749955786	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15814451	GTTTTATTCATTCAA[A/C]TAATAATTCCCCCCA	80013
rs749999263	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15841079	TGTCCAAAAAAATCC[A/G]TTTTTGCAATACCAA	80013
rs750039309	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15857297	GCTGAGTGACTCCAA[C/G]TGTTTGCTCAAATCT	80013
rs750073195	snp	A/C			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15785835	TCAATATGTCTCTCT[A/C]ATAATAGCGGTAAAA	80013
rs750106728	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15799653	ACGGAATCAGGAAAG[A/G]CAGGGAGATGTGACT	80013
rs750119849	in-del	-/CT			intron-variant	FAM188A	GRCh38.p7	10:15807617	GCTTAATGATACTGA[-/CT]CTTAATTAAAACTCA	80013
rs750141340	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15799861	GCACACTACGAACAC[C/T]CACTGTTAGCTAACT	80013
rs750151830	snp	C/T	1.6498e-05	0.00287206	missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15796157	AAGGAGCTTCAGGGG[C/T]AACTAAAGCCATATC	80013
rs750212159	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15804868	TGGTGGTCTTTTCTC[C/T]TATTCTTCCATTATT	80013
rs750221726	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15818892	GGTAAGGAAAACATT[C/T]TGGAATTAGATTGGG	80013
rs750231449	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15795374	TAAGTGTACAAAGTT[C/T]CAAGACAGAAGAAAG	80013
rs750241669	snp	C/G	2.2033e-05	0.00331904	intron-variant	FAM188A	GRCh38.p7	10:15841385	ATTCATTAAAACAAA[C/G]GAACAAGAAAAAAAC	80013
rs750279574	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15787200	AAGAGCTAATGCGTC[A/G]TGAATGACAGTGACT	80013
rs750283225	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15858227	CTACATATCCAAAAT[A/G]TAACTAACTGCACCC	80013
rs750289987	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15806114	ACAGGACTGAAATGT[A/C]AGGGTTGTTGGTTAC	80013
rs750313812	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15830437	AATTCCACACAGTTT[A/G]ATAAATGGCGCAACT	80013
rs750315400	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15817967	GCTAATGTGGCAATG[C/T]TGAGCCAGTAAAGTA	80013
rs750373987	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15825596	TAGGAGTTCCACATA[C/T]TAAGTGGAATATAAC	80013
rs750378005	snp	C/G	1.65233e-05	0.00287426	utr-variant-5-prime, missense, intron-variant, nc-transcript-variant	FAM188A	GRCh38.p7	10:15847929	CAGATCCCTCTGATT[C/G]ACTAAACACAAACCC	80013
rs750426327	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15858956	AAGAGCCCAAGTCAT[G/T]ACATGTAGGGTTTGG	80013
rs750479715	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15805653	TACTTCCTTGCCTCA[C/T]TGACATCAGATTCAG	80013
rs750495269	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15814796	AACCACAAAAGTATC[A/T]GGACAGGTAGGAAGA	80013
rs750548000	snp	C/G	3.18883e-05	0.00399288	utr-variant-5-prime, missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15860213	CAGGGTACCTTGCGT[C/G]CAGCGGCAGAAAATG	80013
rs750569689	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15816558	AAATTCAATTGTTTT[A/C]TCTATAACACAAGTG	80013
rs750572091	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15827465	AGAATTGCTTGAACC[C/T]GGGTTAGGCAGAGGT	80013
rs750608013	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15846178	AGTAGGTTCAGGATT[C/T]TGAATATAACCATCA	80013
rs750712940	snp	A/G	2.1945e-05	0.0033124	intron-variant, downstream-variant-500B	FAM188A	GRCh38.p7	10:15782275	TTATATTTATATCAG[A/G]CAATTTCTAATCAAC	80013
rs750751013	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15791106	ACCATAACTGTACCC[A/G]GTCAGTAACTCTACA	80013
rs750766793	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15802965	ATAAAAAGAGAAAAA[A/G]CCCAAGAGATTATTG	80013
rs750806440	snp	G/T	1.65304e-05	0.00287488	utr-variant-5-prime, synonymous-codon, nc-transcript-variant	FAM188A	GRCh38.p7	10:15841508	CTTTCCTCTTAACCA[G/T]GAAACCAAGCAGTAT	80013
rs750875610	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15789844	ATGAAAGCTGTAGGT[C/T]TAAAAAAAACAGCCC	80013
rs750882369	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15809431	CTGTGCAGTAGGTTC[G/T]CATGTTTTCAAGTAA	80013
rs750894910	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15822485	CAAAGCAGAAGAAAC[A/G]ACAAACAGGTATGAA	80013
rs750939736	snp	C/G			upstream-variant-2KB	FAM188A	GRCh38.p7	10:15862083	CCTTATGTGTAACTT[C/G]CTTATGACAATTCCT	80013
rs750973766	snp	A/G	1.8652e-05	0.00305379	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	FAM188A	GRCh38.p7	10:15778990	ATAAATACTTAGACA[A/G]ATTAATTTAGTGAAG	80013
rs750991237	snp	G/T			utr-variant-3-prime, nc-transcript-variant	FAM188A	GRCh38.p7	10:15778585	TTGTAGAGGCTGATA[G/T]ATTACAAGCCGGAAT	80013
rs751011612	snp	A/G	3.30721e-05	0.00406632	synonymous-codon, intron-variant, nc-transcript-variant	FAM188A	GRCh38.p7	10:15816904	TTTTGGAGATTTCAA[A/G]TAAGAACCAACCTAG	80013
rs751027297	snp	C/G/T			utr-variant-3-prime, nc-transcript-variant	FAM188A	GRCh38.p7	10:15778407	TTTAGAATACATCCC[C/G/T]TATACATCTGTGAAT	80013
rs751137383	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15796999	ACAAACGTCATCAGA[C/G]GGTAAGTTTCCAAGT	80013
rs751175339	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15810554	AAGACTATTCAGCCA[C/T]CTTAAGCACACCTCC	80013
rs751197153	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15840918	GTATGAAAAACTTAA[C/G]GCATAATTAAAATTG	80013
rs751221043	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15849249	ACCTTAATTAAAGCA[A/G]AAAGGTTTTCCAAGA	80013
rs751258022	snp	C/T	1.74054e-05	0.00294998	intron-variant	FAM188A	GRCh38.p7	10:15838197	AATGTGTCCACAGAG[C/T]AAGTATTTTAAATGT	80013
rs751267951	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15801419	TTCTCTGGATCAGTT[A/C]TATCAATGCTGTGTA	80013
rs751289307	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15850946	ACACTTAGGGAAAAT[A/T]GAAAAGAACCTACGT	80013
rs751390196	snp	A/G	5.06154e-05	0.00503042	intron-variant	FAM188A	GRCh38.p7	10:15837327	TCTTTTTCTGGGGGA[A/G]AAAAAGAATTAAGTA	80013
rs751409265	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15817782	TGTTTGTGGCAGTCA[C/G]GCCAAAAATTCTTTC	80013
rs751432144	in-del	-/TAGTA	1.76764e-05	0.00297286	intron-variant	FAM188A	GRCh38.p7	10:15821772	GAAAACTTAGCATTG[-/TAGTA]GTGTGTATAAATTTG	80013
rs751474147	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15800453	TGAGCTTGTGTTGTA[A/T]CTGCTCAGAGCACAA	80013
rs751521811	snp	G/T	3.44774e-05	0.00415181	intron-variant	FAM188A	GRCh38.p7	10:15789360	CTTGAAATAAGAATT[G/T]ACTTCAAGAAATGCT	80013
rs751522077	in-del	-/AGTC	2.6541e-05	0.00364278	utr-variant-5-prime, frameshift-variant, nc-transcript-variant	FAM188A	GRCh38.p7	10:15860285	CTCCATCAGCTCTTT[-/AGTC]AGTTCGGACATGATG	80013
rs751589294	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15795465	TTCTACACGGTACTT[C/T]GTAAGGGAACTCTGA	80013
rs751599044	snp	A/T	3.30093e-05	0.00406246	utr-variant-5-prime, synonymous-codon, intron-variant, nc-transcript-variant	FAM188A	GRCh38.p7	10:15847912	TTCAAACTGTTCTAA[A/T]GCAGATCCCTCTGAT	80013
rs751622051	snp	C/T	4.98749e-05	0.00499349	intron-variant	FAM188A	GRCh38.p7	10:15847817	ACGACAAGTATGAAA[C/T]GTTTCAAAATGTCCC	80013
rs751628106	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15825921	CAAGAGTTGACTCTT[C/G]TATCCCTATCCCATA	80013
rs751650896	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15824508	GGGCATGAGATTAAA[A/C]GGTTTTAGAATCTTC	80013
rs751696763	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15836756	GGAGGAGAGAAAAGA[A/G]CAGGAGGTAACAGAT	80013
rs751754202	snp	C/T	8.9711e-05	0.00669683	intron-variant, downstream-variant-500B	FAM188A	GRCh38.p7	10:15782131	AACCCAGTTGAACAC[C/T]GACGACTACGTGAAT	80013
rs751758661	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15813291	TTCAGTTTGTTCTCA[C/T]CCAAGTTCATCTGTC	80013
rs751765657	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15854031	CTAACACTTGGAAGA[C/T]TGTCATAAACCAGTA	80013
rs751801109	snp	A/G			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15782931	CCCTCTTAACCTGGC[A/G]TTCAAGGCCATTACA	80013
rs751832168	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15853157	AGGGTAGTTGGATCA[A/T]GAATTATTAATTTTG	80013
rs751838176	in-del	-/T			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15782478	TTCAGAACTAACTTA[-/T]TTTTTTTTTAATTAT	80013
rs751843984	snp	A/T	1.72493e-05	0.00293672	intron-variant	FAM188A	GRCh38.p7	10:15833716	AAACTTTGGCTATTA[A/T]TAAATATTAAAAAGC	80013
rs751866828	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15805735	TAAGTGCCACTATCT[A/G]GTTTGGCCAGAAGTC	80013
rs751910534	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15788281	TTAAATTGAAAACAA[C/T]TATTCATTTATTAAT	80013
rs751927621	in-del	-/AAC			intron-variant	FAM188A	GRCh38.p7	10:15839771	CTCAAATTTTCAGTT[-/AAC]AAAGTATTTCAAATG	80013
rs752033337	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15801176	AAGGTGTCCTATTCC[A/G]GCATGGGGGGGAAAT	80013
rs752103602	snp	C/T			upstream-variant-2KB	FAM188A	GRCh38.p7	10:15860544	TCTTTAACTCCCGCC[C/T]CTTAAGGCTGAGGGC	80013
rs752139606	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15789610	ACAGCGTTAAGTGGG[G/T]AAAATATTTTTCTAC	80013
rs752147676	snp	A/G	0.000100189	0.00707705	intron-variant	FAM188A	GRCh38.p7	10:15841404	CAAGAAAAAAACTTC[A/G]GGAAATAAAAATATA	80013
rs752248375	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15807645	CTCATAGGCTTCATT[C/T]CTAACAGAATACTTC	80013
rs752256227	snp	C/T			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15785610	TCGGACAATAAAATC[C/T]AATTTTTCATGAAGG	80013
rs752269937	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15831783	CGGGTTCAAGCAATT[A/C]TCCTGCCTCAGCTTC	80013
rs752303921	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15788182	TGTAAACAACATGGT[C/G]TCTACTTGGAAATAA	80013
rs752333808	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15850005	GGACCTGCTGAAGCT[A/G]TGACAGAAGAATATA	80013
rs752344094	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15821876	AAAACTTAGCATGTA[A/T]TCATTACAGTACTGC	80013
rs752357138	in-del	-/TT			intron-variant	FAM188A	GRCh38.p7	10:15823564	ATATTAATGAGTATA[-/TT]TTGTTTTTTTCTAAA	80013
rs752377370	snp	A/T	1.96578e-05	0.00313504	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	FAM188A	GRCh38.p7	10:15778984	TTCCTTATAAATACT[A/T]AGACAAATTAATTTA	80013
rs752401417	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15840652	GAATAAGTCACTTAT[A/T]TAACATAAGCACTTG	80013
rs752448966	snp	C/T	1.69009e-05	0.00290692	intron-variant	FAM188A	GRCh38.p7	10:15821608	CAGTATCCACAATAG[C/T]GGACATCTAAACAAA	80013
rs752547252	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15808919	ACTATTTTTATACTG[C/G]ATCAACAGCTGTCAC	80013
rs752563613	snp	C/T	3.35177e-05	0.00409362	utr-variant-5-prime, nc-transcript-variant	FAM188A	GRCh38.p7	10:15860330	GGCGGATCTTCGCTT[C/T]GCGGACTCCTGCCCC	80013
rs752572015	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15849680	GTTTCTAGTTTGAGA[A/C]ACCAGGTGAGAGCAA	80013
rs752592031	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15839004	ACAGAAAAATCCTCT[C/T]AAGAGTACATAGGAT	80013
rs752638854	snp	A/G	1.68788e-05	0.00290501	intron-variant	FAM188A	GRCh38.p7	10:15837325	GATCTTTTTCTGGGG[A/G]AAAAAAAGAATTAAG	80013
rs752707409	snp	A/G			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15784125	TGACCTTCAACAATC[A/G]TCTTAAGTTCTCTAA	80013
rs752713023	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15793165	AATACGAAGCACATA[G/T]CCAAACATTTTCTTC	80013
rs752716085	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15829383	ATGCCCAGATTCCAG[C/G]TGACAACAATTCCAT	80013
rs752740358	snp	C/T			synonymous-codon, nc-transcript-variant	FAM188A	GRCh38.p7	10:15796101	TTAAAATCTTTTACC[C/T]TCTGGGTCGTAGGTT	80013
rs752744317	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15802967	AAAAAGAGAAAAAAC[C/T]CAAGAGATTATTGTA	80013
rs752745533	in-del	-/AAC	0.0179999	0.0931448	intron-variant	FAM188A	GRCh38.p7	10:15821734	AGAAGTTCTGCAAAA[-/AAC]AACAACAACAACAAC	80013
rs752746552	snp	C/T	8.38104e-05	0.00647288	intron-variant	FAM188A	GRCh38.p7	10:15786671	GAGAAAGAAGAAAAA[C/T]AGTGGATACCAGAGG	80013
rs752773712	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15834178	GCTTGAGGAGGGTGG[A/T]CCGAGAGGAAAATGG	80013
rs752790383	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15835425	AAGATTTTTAAAGAA[A/T]GACTAAATCCCGCAG	80013
rs752936969	snp	A/G	0.000182741	0.00955704	synonymous-codon, downstream-variant-500B, nc-transcript-variant	FAM188A	GRCh38.p7	10:15779133	TGCAGTCCCTTCTAC[A/G]TACATGACCTGTTGA	80013
rs752944209	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15794240	TGCTTGTAAGAACTT[A/T]CTGCATACTAAGTGT	80013
rs752949485	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15799993	TTCCTTCAAAGAACT[A/G]AGAAGCGAGTACAGT	80013
rs752986454	in-del	-/A			intron-variant	FAM188A	GRCh38.p7	10:15816519	TTTTATCCTACTTAC[-/A]AAAAAAAGCAATCTA	80013
rs753025159	snp	A/G/T	4.99416e-05	0.00499687	intron-variant	FAM188A	GRCh38.p7	10:15833581	ATCAGCTGTATTCCA[A/G/T]TGAAATATTATTCAT	80013
rs753037823	snp	C/T	3.3042e-05	0.00406447	synonymous-codon, nc-transcript-variant	FAM188A	GRCh38.p7	10:15833685	AACAGCATGTCCCGT[C/T]AGCAGGAGATTAATT	80013
rs753049496	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15781651	AGCTCTGTCATTTCC[G/T]GGCTGCTTGACCTGT	80013
rs753055465	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15853096	CGAACACCAACAGAC[A/T]ACTATATTTAAGTTT	80013
rs753066861	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15810343	GCAATTTTCTTAACC[A/G]TCCTCAAATCATGAA	80013
rs753078960	snp	A/G	1.64898e-05	0.00287135	utr-variant-5-prime, missense, intron-variant, nc-transcript-variant	FAM188A	GRCh38.p7	10:15847880	TGAACAGGTGCAATA[A/G]CAGCACAGGGGCCAC	80013
rs753094087	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15813242	TCTTACACCTTGTCC[C/G]CCTAATTCTCAGTGC	80013
rs753142442	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15844914	GAGCATCCTGATTAT[G/T]TGGCTGTAAAGCATC	80013
rs753154687	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15806612	TTACATTCATGCCAC[A/G]GATATTCCTGTTTAG	80013
rs753169262	in-del	-/ATCTT			intron-variant	FAM188A	GRCh38.p7	10:15799549	GGGGGGAGTAAAGAC[-/ATCTT]AATCACTTTTACAGA	80013
rs753230624	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15843703	ATCTGTGACACAAGA[C/T]TAACACTATTAGAGT	80013
rs753258185	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15830724	CTTCAGGGAGAATGA[C/G]GGGTAGGAAAAAGGC	80013
rs753365702	in-del	-/T	1.65323e-05	0.00287505	frameshift-variant, intron-variant, nc-transcript-variant	FAM188A	GRCh38.p7	10:15786575	CTGATCAGGAAAAAA[-/T]TTCTTGAAGAAATGG	80013
rs753381152	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15843491	TAGATTCATAAAATT[A/C]TTCTTCTTCCACAAT	80013
rs753406925	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15843536	AAGTAGAAGAACTAA[C/T]TCACATAACAGAATA	80013
rs753421875	snp	C/G	1.6691e-05	0.00288881	intron-variant, synonymous-codon, utr-variant-5-prime, nc-transcript-variant	FAM188A	GRCh38.p7	10:15838254	ATGAAATCGCTCAAA[C/G]CCAAGCTCTTCGACA	80013
rs753446705	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15799878	ACTGTTAGCTAACTG[C/T]GAGCTTCTCGTGAGC	80013
rs753464168	snp	C/T	1.65225e-05	0.00287419	stop-gained, intron-variant, nc-transcript-variant	FAM188A	GRCh38.p7	10:15816877	CTCACTGCCAACAAT[C/T]CAAATAGGGAATTTT	80013
rs753493734	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15795056	CAAAACACAACACAA[C/T]ACATAACGATTACAT	80013
rs753494024	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15818951	TTAAAAAGCCCTGAA[C/T]TGTATGCTTTAAAAT	80013
rs753514959	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15788039	GATAAAACAAGGAAA[A/T]TTAGGTAGATGATAT	80013
rs753554753	snp	C/G	1.65444e-05	0.00287609	intron-variant	FAM188A	GRCh38.p7	10:15796204	CATGTTGTCAACCAG[C/G]TACAGTATTATGACA	80013
rs753616701	in-del	-/T			intron-variant	FAM188A	GRCh38.p7	10:15810259	TTTAATTACTTTAAG[-/T]TCCTAAAAGTAAATT	80013
rs753671220	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15819971	AATACGTCCATTCAT[C/T]CATTCAACAAATATT	80013
rs753672842	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15807500	GTAAGACTTAGTGGC[A/G]GTCATCTATTAACCA	80013
rs753675131	snp	A/G	2.65059e-05	0.00364036	utr-variant-5-prime, missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15860235	CAGAAAATGGTGTCC[A/G]AGAGACCGGGGCTGC	80013
rs753714093	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15849107	TGTTATAAGAGAAGA[A/G]TGCAGAGTATTGTGG	80013
rs753869492	snp	C/T	1.65641e-05	0.00287781	missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15834544	TTTTAGTTAATTACC[C/T]GCCATGTCCATATAC	80013
rs753869637	snp	A/G	0.000143441	0.00846758	utr-variant-5-prime, nc-transcript-variant	FAM188A	GRCh38.p7	10:15860316	ATGAGGAACCGGCGG[A/G]CGGATCTTCGCTTTG	80013
rs753968283	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15835245	CAACTCCCAAAAGTT[A/C]TACATACTGGATAAG	80013
rs753972770	in-del	-/AAA			intron-variant	FAM188A	GRCh38.p7	10:15849791	TTTATCTAACATATT[-/AAA]ATAAAACAAAACAAA	80013
rs753986883	snp	A/T	1.66076e-05	0.00288158	missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15837232	ACAGAATACAGAAAA[A/T]GCAATACTCCAAATT	80013
rs754052595	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15834133	AACTATCACTGTTTC[A/G]TTGAGTTTTGGTAAA	80013
rs754062595	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15832866	AATGGGAGCAAAAAG[A/T]GGTAACTATTATTTT	80013
rs754095148	snp	C/T	3.34599e-05	0.00409009	intron-variant	FAM188A	GRCh38.p7	10:15821639	AAACATTCAAAGTAC[C/T]TTAAAAATCAATTTA	80013
rs754097822	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15804470	ACTGAAAAGGTCTTT[A/G]AAGTTTTTCTCATTA	80013
rs754124475	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15781116	AAACAACATCCAAGT[A/T]TGCATATATATATAC	80013
rs754137889	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15859854	AGGGGGTAAAGATGC[A/G]GAAGGCCACAGCACC	80013
rs754146733	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15833371	GAGTCATAAATCCCA[C/G]TTTTATACCACAGAA	80013
rs754152262	snp	C/T			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15779894	ATTTACAATGAAACA[C/T]ACTTAAAAAGTATTT	80013
rs754169915	in-del	-/ACA			intron-variant	FAM188A	GRCh38.p7	10:15794860	AATTTTTTCAGCCTT[-/ACA]ACATCAGCCTTCTAA	80013
rs754176255	snp	C/T	1.65247e-05	0.00287438	intron-variant	FAM188A	GRCh38.p7	10:15843283	AATGCCTTTACACAA[C/T]TAAAGCAATAATTAG	80013
rs754189127	snp	A/G	1.65479e-05	0.0028764	intron-variant	FAM188A	GRCh38.p7	10:15843176	CTCTATTAAAACAGA[A/G]GAGGAAGCAAAAGTT	80013
rs754232292	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15823747	ATTGAATTTACTCCA[C/T]GTTACAGTATGTTTG	80013
rs754273732	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15853001	AGTGTAGGGGAAGTC[A/G]TGTGTAGGTTATATG	80013
rs754307134	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15842285	TTCTGTCTCTCCTAA[C/T]GGATTAACAGTTCTT	80013
rs754318464	in-del	-/TTG			intron-variant	FAM188A	GRCh38.p7	10:15793069	AGAGGCACTAGAGAA[-/TTG]TTGTTGTCCAGTATC	80013
rs754320163	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15822734	AATACAGGAGAGAAA[C/T]GTCAGGGTTGGAGAT	80013
rs754329367	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15812513	TGGTTCCTTTGGCAT[A/G]AAGAATAGATGTGGG	80013
rs754361829	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15852116	CTCTCCTGTCATCCC[C/G]TAGCACAACCAGTAC	80013
rs754375437	snp	C/T	1.6582e-05	0.00287936	missense, downstream-variant-500B, nc-transcript-variant	FAM188A	GRCh38.p7	10:15779108	TGGGATCTTCAAAAC[C/T]CATCACAACTGCAGT	80013
rs754421604	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15810672	ACAAAAAGTCATTGA[A/G]CACCTACACTATGCC	80013
rs754441535	in-del	-/AAGA	4.99821e-05	0.00499885	intron-variant	FAM188A	GRCh38.p7	10:15786663	ACTACGGGGAGAAAG[-/AAGA]AAAACAGTGGATACC	80013
rs754468551	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15830803	ACAGATTTCAGATCA[C/T]AGAGAGTAAATATTT	80013
rs754469748	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15858343	GGTGGCAGAGCGTTC[C/T]AATAAGTCATTATAA	80013
rs754476975	snp	C/G/T	8.27443e-05	0.00643165	intron-variant	FAM188A	GRCh38.p7	10:15796207	GTTGTCAACCAGCTA[C/G/T]AGTATTATGACATTA	80013
rs754498670	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15787363	CTGCAGTTTAATGGG[C/T]TTAAAAATGAAAATA	80013
rs754514925	snp	A/T			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15785431	CAGGAATATTCTTTT[A/T]ATTATAACTAAGAAT	80013
rs754540020	snp	C/T	1.65081e-05	0.00287293	intron-variant	FAM188A	GRCh38.p7	10:15796058	AATGTATTTCAAACA[C/T]ATGAAGACATAAAAC	80013
rs754552812	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15849168	ACAGATAACTTCCAG[A/G]CTCATCTTGAACAGG	80013
rs754574158	snp	A/C	4.17423e-05	0.00456831	intron-variant	FAM188A	GRCh38.p7	10:15841399	AGGAACAAGAAAAAA[A/C]CTTCAGGAAATAAAA	80013
rs754604264	snp	C/T	1.82264e-05	0.00301875	intron-variant, downstream-variant-500B	FAM188A	GRCh38.p7	10:15782119	AATTATTTCATCAAC[C/T]CAGTTGAACACCGAC	80013
rs754631560	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15836022	CAAACTTTTTACTGT[A/G]TTCCAATTCTGAGCA	80013
rs754673800	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15806710	GGTCCTACAGCTGAT[C/T]GTCAACCTTTGGTTT	80013
rs754683473	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15836845	TAGAAAGAAAACTCA[A/C]ACAGTGATTTTTCAA	80013
rs754698047	in-del	-/G			intron-variant	FAM188A	GRCh38.p7	10:15814913	AGCTCATTCGACACT[-/G]TTCCTTGTATTATAC	80013
rs754788047	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15847072	GCCACATTAAATATA[C/T]ATATTTTCAAAACAC	80013
rs754796459	snp	A/G	9.9686e-05	0.00705925	utr-variant-5-prime, nc-transcript-variant	FAM188A	GRCh38.p7	10:15860319	AGGAACCGGCGGGCG[A/G]ATCTTCGCTTTGCGG	80013
rs754800510	snp	C/T	1.65553e-05	0.00287705	missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15834589	GTTCACTTGCATCTT[C/T]AATTTCGTTTTTTAT	80013
rs754800865	in-del	-/AAAGT			intron-variant	FAM188A	GRCh38.p7	10:15819916	CCTAAAAATTAAAGC[-/AAAGT]AAAGCCTACATCTAG	80013
rs754868049	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15807527	ACCATACAAGACCTT[G/T]TTTTGTACTCTGCTA	80013
rs754890412	snp	A/G	2.6108e-05	0.00361293	utr-variant-5-prime, synonymous-codon, nc-transcript-variant	FAM188A	GRCh38.p7	10:15860237	GAAAATGGTGTCCGA[A/G]AGACCGGGGCTGCTC	80013
rs754898026	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15813497	CCTGTGCTTTGTCAG[C/G]ACTCATCACACTTGT	80013
rs754899668	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15827545	GAGACTCCGTCTCAA[C/T]AAATAAATAAATAAA	80013
rs754905294	snp	A/G	1.65908e-05	0.00288012	intron-variant	FAM188A	GRCh38.p7	10:15786536	CAACAGAATAACAAT[A/G]AATATATTTCCTCAA	80013
rs754924301	snp	C/T	4.96446e-05	0.00498195	missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15837250	AATACTCCAAATTTA[C/T]TTCCCCACATTGAAT	80013
rs755007932	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15795865	GGTCAAGATTAATCA[A/G]AGGGGTCAACTACAC	80013
rs755066959	in-del	-/T			intron-variant	FAM188A	GRCh38.p7	10:15857600	GAGAAGAATAAATTT[-/T]CACGTTAAAATAAAA	80013
rs755155733	in-del	-/TA	1.65781e-05	0.00287902	frameshift-variant, nc-transcript-variant	FAM188A	GRCh38.p7	10:15834602	TTCAATTTCGTTTTT[-/TA]TGTTTTCAATGCCCT	80013
rs755162920	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15853316	TCCTAGAGACCTTTC[A/T]GGGGGCCCACTGGAA	80013
rs755197911	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15791520	ATAGATATCAACACA[A/G]AAGAATGGGGACTAT	80013
rs755253586	snp	C/T	1.68838e-05	0.00290544	intron-variant	FAM188A	GRCh38.p7	10:15821614	CCACAATAGTGGACA[C/T]CTAAACAAAAAACAT	80013
rs755265403	snp	C/T	5.30143e-05	0.00514824	intron-variant	FAM188A	GRCh38.p7	10:15821772	GAAAACTTAGCATTG[C/T]AGTAGTGTGTATAAA	80013
rs755364794	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15851196	AAGTGCTAATGTTCC[C/T]CAGGTCTTGGTTTTA	80013
rs755371906	snp	C/T	1.69055e-05	0.00290731	missense, downstream-variant-500B, nc-transcript-variant	FAM188A	GRCh38.p7	10:15779015	GTGAAGGAGAGCGAT[C/T]TGTGGTCCAGAGTAA	80013
rs755376836	snp	A/G			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15780012	CCAAGAGAAATTCTG[A/G]TGCTGTATAATTTAA	80013
rs755411136	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15810799	ACAAGTAAATATACA[A/G]GACGAATCTAGTACC	80013
rs755420747	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15829613	TTAGCAAGAGAGTCA[C/T]TGAAGGCACTGAGCA	80013
rs755429527	snp	C/T	4.9958e-05	0.00499765	intron-variant	FAM188A	GRCh38.p7	10:15821653	CCTTAAAAATCAATT[C/T]ACCTTACAGTATCTT	80013
rs755437117	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15799903	GTGAGCTATTAGAAA[C/T]AGAATATTAGTGTTA	80013
rs755452559	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15843553	CACATAACAGAATAA[C/G]TGAAAAGCACACAAA	80013
rs755489712	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15836232	TACTTGCAGTGCCCA[C/G]TGCTGGAAAAAATGT	80013
rs755559353	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15798544	GGACTTTGGGAGGCC[A/G]AGGTGGGCAGATAAC	80013
rs755602194	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15842237	GTAGTATTACTTTCT[A/G]AAACTTTCAAAAATT	80013
rs755637612	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15828921	CCTTAGGTAAGCTGC[C/T]TTACCTCTCTAGGCT	80013
rs755642470	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15798264	TAGTAGAAATGTAAC[C/T]GAAGCGTTACTTCAA	80013
rs755657761	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15788968	TTAAGACGTGGGGAA[C/G]TGTTTGCAGAGAAAC	80013
rs755670072	in-del	-/T			intron-variant	FAM188A	GRCh38.p7	10:15808650	CTCCTTAGCATTAAA[-/T]TCAGTTTCTTTATAT	80013
rs755725911	snp	G/T	1.7309e-05	0.0029418	intron-variant	FAM188A	GRCh38.p7	10:15789363	GAAATAAGAATTTAC[G/T]TCAAGAAATGCTATT	80013
rs755801984	snp	A/G			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15786026	ACTGGCTTGCCAATG[A/G]TGCAGATACAACTCA	80013
rs755819462	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15818095	GAGGTGAGCTGTGCA[A/G]GTCCTTCAATTTATA	80013
rs755845888	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15848314	TCTATCATTTCAAAC[G/T]TTCTGTCACATTCTA	80013
rs755916965	snp	C/G	3.30229e-05	0.0040633	intron-variant	FAM188A	GRCh38.p7	10:15796180	GCCATATCCTGAAAA[C/G]ATAAGAAGCATGTTG	80013
rs755957684	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15852289	TGTTTTGGCATGGAA[G/T]ATAATGGCAGTGTTT	80013
rs755977931	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15809065	CATTTTGAATTTGCA[C/T]TGAAAATTAATTTCC	80013
rs756025137	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15836786	TAAAGAAGGAAACAA[A/G]GCTATCAAAGAAAAC	80013
rs756049353	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15849850	ATCAGCACTCCATCA[C/T]TCTTGTCCTCCCAAA	80013
rs756052876	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15793291	GAGTAAGTGTGCTAG[C/T]CTCCCCTTTCTGAAT	80013
rs756053088	snp	A/G	2.97889e-05	0.00385922	utr-variant-5-prime, synonymous-codon, nc-transcript-variant	FAM188A	GRCh38.p7	10:15860219	ACCTTGCGTCCAGCG[A/G]CAGAAAATGGTGTCC	80013
rs756072601	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15794474	CCTAAGTCATATATA[C/G]AGGCATACTTTCTAA	80013
rs756086537	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15855102	ATCCACAGGTGGGGC[G/T]TTCAGTTGGAAATGC	80013
rs756101484	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15806174	CTAATATTCTGGCTG[A/G]GGCTGTATGTTGCTT	80013
rs756206677	snp	A/G	1.66112e-05	0.00288189	intron-variant	FAM188A	GRCh38.p7	10:15834524	TCACATGAGGAGACA[A/G]GAGATTTTAGTTAAT	80013
rs756259071	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15801374	CCAATCTTTTGGCTG[C/T]ATAAGAAAGAAGGCC	80013
rs756277604	snp	C/T	1.75394e-05	0.00296132	intron-variant, downstream-variant-500B	FAM188A	GRCh38.p7	10:15782138	TTGAACACCGACGAC[C/T]ACGTGAATTATCATA	80013
rs756291363	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15854110	GAGGTAAGAGATCTA[C/T]TAAAACTGCAAGACA	80013
rs756312769	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15802282	CACTGCTATAAAGAT[A/G]CTACCTGAGGTGGGG	80013
rs756385532	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15833157	TTGAGACCAGAAATG[C/G]AAGTGGTAGTGGAAG	80013
rs756416850	snp	A/G	1.74488e-05	0.00295366	intron-variant	FAM188A	GRCh38.p7	10:15841650	CTCTGGAAAAAAAAA[A/G]ATTCTGTCATGAATA	80013
rs756428077	in-del	-/A			intron-variant	FAM188A	GRCh38.p7	10:15789329	CATTATCTAGGGGGG[-/A]AAAAATCAGAAACAA	80013
rs756461451	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15821539	ATAGGAAGGAAGAAG[A/G]GAGCGGTACTGAACC	80013
rs756491291	snp	A/C			upstream-variant-2KB	FAM188A	GRCh38.p7	10:15860726	CAGGAATACCTTCTT[A/C]CTCTACGCACTGCTC	80013
rs756528150	snp	A/G	1.65425e-05	0.00287593	missense, intron-variant, nc-transcript-variant	FAM188A	GRCh38.p7	10:15816908	GGAGATTTCAAGTAA[A/G]AACCAACCTAGAACA	80013
rs756540373	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15810510	TTGCCCTCCATGTAA[C/G]ATAGAGATCTATTGA	80013
rs756546154	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15797203	GAGCCATGAGGACTC[G/T]ATTCCTGAAAACCTT	80013
rs756549784	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15841119	TTAAGGCATCTGAAA[C/G]TGAAGCATATCATTA	80013
rs756571846	snp	C/T	4.95864e-05	0.00497903	utr-variant-5-prime, synonymous-codon, nc-transcript-variant	FAM188A	GRCh38.p7	10:15841514	TCTTAACCATGAAAC[C/T]AAGCAGTATGATCCA	80013
rs756629911	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15806801	CAAACACAGTATTAA[C/G]TTTCCCATTATAACA	80013
rs756637511	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15851092	ATCAATCTGAAATGC[A/T]GACCACAAACCTGCG	80013
rs756652865	snp	A/T	1.68199e-05	0.00289994	intron-variant	FAM188A	GRCh38.p7	10:15821628	ATCTAAACAAAAAAC[A/T]TTCAAAGTACCTTAA	80013
rs756694461	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15810778	GAGAGACAGATAATA[C/T]AGAAAACAAGTAAAT	80013
rs756777547	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15839181	ATTATGAAGTCAAAA[G/T]TTTAGATTTTTATTT	80013
rs756794863	snp	A/G	5.06103e-05	0.00503017	intron-variant	FAM188A	GRCh38.p7	10:15837329	TTTTTCTGGGGGAAA[A/G]AAAGAATTAAGTATT	80013
rs756803252	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15809314	CACAGCCTTCATCTA[A/G]TAAGAGCTAGTTTTT	80013
rs756825657	snp	A/G	6.77805e-05	0.00582114	utr-variant-5-prime, nc-transcript-variant	FAM188A	GRCh38.p7	10:15860349	GACTCCTGCCCCGGA[A/G]CATGGGGAAGGGGCA	80013
rs756941728	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15846639	CTACAGAAATATATT[C/T]TTAATAATGTAAGTA	80013
rs756989430	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15857093	TAATGGCCTAGAAAG[C/T]TTTATATGATTTGGG	80013
rs757021886	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15789683	TACATTTGCATTTAA[A/C]AATTCAATTAAAATA	80013
rs757047305	snp	A/G	1.72749e-05	0.0029389	intron-variant	FAM188A	GRCh38.p7	10:15789361	TTGAAATAAGAATTT[A/G]CTTCAAGAAATGCTA	80013
rs757062421	snp	A/T	6.70421e-05	0.00578935	missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15789255	AGCTTACTATTCAGG[A/T]TCTGAAACAAGGTCC	80013
rs757088022	in-del	-/AGG	1.65291e-05	0.00287476	cds-indel, nc-transcript-variant	FAM188A	GRCh38.p7	10:15833689	GCATGTCCCGTCAGC[-/AGG]AGATTAATTAAACTT	80013
rs757107904	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15786872	TAAAATTTAAATTGT[C/G]ATGACTTTGGAATAT	80013
rs757135881	in-del	-/AC			intron-variant	FAM188A	GRCh38.p7	10:15822337	GTGGTCTCTCTGTAC[-/AC]ACACACACACACGGA	80013
rs757149935	snp	A/G	3.32287e-05	0.00407593	intron-variant	FAM188A	GRCh38.p7	10:15847818	CGACAAGTATGAAAC[A/G]TTTCAAAATGTCCCT	80013
rs757160303	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15803375	TATACTGCATATTTG[A/C]ATAGCAAGTTTGAAG	80013
rs757185595	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15791654	GTTGGTTTAAAATTT[A/T]AAAAGATTTTTACCA	80013
rs757194953	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15834224	CAAGCAGAGAAGCAC[G/T]TACAAAGATATACTT	80013
rs757195780	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15822109	ACTTTGATTTTGAAA[A/G]ACAAATGGATATGCT	80013
rs757217375	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15804722	AGTCTTTGCTTACTA[C/T]CTGTATTTATGAACA	80013
rs757250725	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15847427	AGTATAAGCTGCCAA[C/G]TTTTTTCAAATTTGA	80013
rs757293713	snp	C/T	1.75133e-05	0.00295911	intron-variant	FAM188A	GRCh38.p7	10:15833721	TTGGCTATTAATAAA[C/T]ATTAAAAAGCAATTA	80013
rs757323655	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15812697	ATAGCTCTCCACATG[C/T]CTGTCTGAGAGGTAC	80013
rs757340553	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15781977	TGTCAGTTTCCAATG[C/T]AGACTAACATATACT	80013
rs757394012	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15803064	TGATTACTGGCTTGC[C/T]TATTTTGACTGTTTA	80013
rs757434545	snp	A/G	1.78455e-05	0.00298704	intron-variant, downstream-variant-500B	FAM188A	GRCh38.p7	10:15782132	ACCCAGTTGAACACC[A/G]ACGACTACGTGAATT	80013
rs757437546	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15813317	CTGTCTGTCTGTCCT[C/T]CTTTCTTCAGGCATG	80013
rs757621245	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15854044	GATTGTCATAAACCA[A/G]TAGACTGATAATCTC	80013
rs757635397	snp	C/T	2.0976e-05	0.00323845	intron-variant, downstream-variant-500B	FAM188A	GRCh38.p7	10:15782267	ACTTTAAATTATATT[C/T]ATATCAGGCAATTTC	80013
rs757658272	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15830186	TTCTATAAAGGGCAG[C/T]TACAACTACTGATGA	80013
rs757662761	snp	C/T	1.6577e-05	0.00287893	intron-variant	FAM188A	GRCh38.p7	10:15796220	TACAGTATTATGACA[C/T]TAAAAAGAAAACAGA	80013
rs757670501	snp	A/T	0.000155915	0.00882798	intron-variant	FAM188A	GRCh38.p7	10:15841407	GAAAAAAACTTCAGG[A/T]AATAAAAATATATCT	80013
rs757675271	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15850225	GCTGAGCATGTATGT[C/T]GCCTCAGGATCCTGT	80013
rs757685871	in-del	-/A			intron-variant	FAM188A	GRCh38.p7	10:15860029	ACCATTCTCCTACTC[-/A]AACTCTCCCCACCAA	80013
rs757751633	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15821449	GACAAAAATAACAAC[A/T]GACCTAGCATAGGAA	80013
rs757751755	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15807870	GGCAAAGAGTACATA[A/T]GGGTAACTGATGTTC	80013
rs757761384	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15799613	CAGAAATAGAAAAGA[A/G]GGCACAGAATTCTAG	80013
rs757768160	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15820460	ACTTGCCCCACCCCC[C/T]GCCTCCATGCTTAAC	80013
rs757802084	in-del	-/A			intron-variant	FAM188A	GRCh38.p7	10:15814256	TTTTATTTCAAGGGG[-/A]AAAAAACAACTCTTC	80013
rs757885464	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15806827	TAACACTACATCTAT[A/G]CAGCTTTCACTTCAT	80013
rs757926075	snp	A/G			utr-variant-5-prime, nc-transcript-variant	FAM188A	GRCh38.p7	10:15860469	GACCAAGCCTGTCAA[A/G]CCAGGTTGGGGCAGC	80013
rs757935235	snp	C/G	3.30589e-05	0.00406551	missense, intron-variant, nc-transcript-variant	FAM188A	GRCh38.p7	10:15816894	AAATAGGGAATTTTG[C/G]AGATTTCAAGTAAGA	80013
rs757958614	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15817407	AACCATTTAAGTATG[C/T]AAGTGTCCTGTTATT	80013
rs758043690	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15826414	ATGGATTCAGGACCA[C/T]ATAATCTATATAAAA	80013
rs758059387	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15854278	GAAAAGGCTACTACC[A/G]TACTTCTCATGCCTT	80013
rs758088449	snp	A/G	7.65101e-05	0.00618459	utr-variant-5-prime, synonymous-codon, nc-transcript-variant	FAM188A	GRCh38.p7	10:15860243	GGTGTCCGAGAGACC[A/G]GGGCTGCTCTTGGTG	80013
rs758122252	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15795919	AAACCCAACTCAACA[A/G]GGACTTGTGTGCTAT	80013
rs758140492	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15846722	CCAACAGTTTAGGAA[G/T]GCATTTTTTTTTTTT	80013
rs758145277	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15796947	TCTGGTTAGCTTTTA[C/T]CTATAATTGTCTTTG	80013
rs758178221	snp	A/G/T	3.3756e-05	0.00410817	intron-variant	FAM188A	GRCh38.p7	10:15837326	ATCTTTTTCTGGGGG[A/G/T]AAAAAAGAATTAAGT	80013
rs758181937	snp	C/T	1.65441e-05	0.00287607	utr-variant-5-prime, synonymous-codon, nc-transcript-variant	FAM188A	GRCh38.p7	10:15837261	TTTATTTCCCCACAT[C/T]GAATACTGGTCCAAG	80013
rs758234455	snp	G/T	1.6766e-05	0.00289529	intron-variant	FAM188A	GRCh38.p7	10:15786674	AAAGAAGAAAAACAG[G/T]GGATACCAGAGGAAA	80013
rs758270320	in-del	-/CACATCTTC	1.66776e-05	0.00288765	cds-indel, nc-transcript-variant	FAM188A	GRCh38.p7	10:15789281	GTCCAATGCTTTCAT[-/CACATCTTC]CACATCTTCCAGAAG	80013
rs758272069	in-del	-/A/AAA	5.08449e-05	0.00504181	intron-variant	FAM188A	GRCh38.p7	10:15821749	AACAACAACAACAAC[-/A/AAA]AAAAAACGAAAACTT	80013
rs758329580	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15846503	ATAATTCCAAGGCAA[G/T]ATTCAGACATTCAAA	80013
rs758352891	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15790523	TTTGATGAGTCTGAT[C/G]ACTGATTTTGCTTAA	80013
rs758367924	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15835435	AAGAATGACTAAATC[C/T]CGCAGGGGGAAACAA	80013
rs758424696	in-del	-/AAAC			intron-variant	FAM188A	GRCh38.p7	10:15792703	GCAACTTAACAAAAC[-/AAAC]AAACAGCTTCAGATT	80013
rs758558811	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15824456	TAACATGAAAAACAT[G/T]GATTATTTGCTTTGG	80013
rs758569310	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15803458	ACTTCAGAGGTATAA[A/C]TGCCGTATTTTTCTT	80013
rs758583353	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15842453	ATTTCAAAAATAGTA[A/T]CTCAAATAGTTTCTT	80013
rs758603311	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15781679	TGTAAAATGGAGATA[C/T]ACAGACAACACTTCC	80013
rs758662296	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15835980	AGATATCTTTTATCA[A/G]CAAAAAGATCTTGTC	80013
rs758662478	in-del	-/G			intron-variant	FAM188A	GRCh38.p7	10:15843428	CCCTCACATTTGACA[-/G]GAACTGTGCAGTTAT	80013
rs758685594	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15812644	ACTGCTCTTTGGAGG[C/G]AAATACAAGAAGAAA	80013
rs758704302	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15811079	GTTTTCAAACTCTGC[C/G]AATTATTTTGATAAT	80013
rs758711672	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15843717	ATTAACACTATTAGA[C/G]TCATCACTTTATTAT	80013
rs758754012	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15801680	CTATTAAAGAGAACC[A/G]CAACAGCAAGAACAA	80013
rs758762583	snp	A/C	1.66996e-05	0.00288956	intron-variant, stop-gained, utr-variant-5-prime, nc-transcript-variant	FAM188A	GRCh38.p7	10:15838265	CAAAGCCAAGCTCTT[A/C]GACAGCCAAGGCAGC	80013
rs758859719	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15799998	TCAAAGAACTAAGAA[G/T]CGAGTACAGTTGATC	80013
rs758861244	in-del	-/A			intron-variant	FAM188A	GRCh38.p7	10:15799699	AAACTGAAAAAGGTG[-/A]ACAGGACTGAGAACT	80013
rs758879951	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15813260	TAATTCTCAGTGCTC[C/G]CTCCAGCCCTTGTCT	80013
rs758937846	snp	C/G	1.65534e-05	0.00287688	utr-variant-5-prime, missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15841476	CTCCCAGAAATACTA[C/G]CAGTTTCCTCAGTTG	80013
rs759010466	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15788161	CTCTTTTGTAAATTA[C/G]AGCAGTGTAAACAAC	80013
rs759020100	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15858652	CTGAACCAAGTACAT[A/C]TATTCCAGACTGTGC	80013
rs759060381	snp	C/G/T	4.95707e-05	0.00497828	missense, intron-variant, nc-transcript-variant	FAM188A	GRCh38.p7	10:15816882	TGCCAACAATCCAAA[C/G/T]AGGGAATTTTGGAGA	80013
rs759105241	in-del	-/AAAG	2.21835e-05	0.00333036	intron-variant	FAM188A	GRCh38.p7	10:15841382	TAGATTCATTAAAAC[-/AAAG]GAACAAGAAAAAAAC	80013
rs759105448	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15820062	CATTAGGGAAGACAA[C/T]AGAAAAGCAAATTCA	80013
rs759133323	in-del	-/AAAC	3.41775e-05	0.00413371	intron-variant	FAM188A	GRCh38.p7	10:15816946	CAAAATAAAACAAAT[-/AAAC]AAATTAAAAATTTAT	80013
rs759151670	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15854416	GATAAACATTAAAGA[A/G]ATTAGCAAAAATGTA	80013
rs759171549	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15789005	AAGTTTATAGAAAGA[C/T]ACTTTTAGCATTTTT	80013
rs759198280	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15845938	AGTGATTCTCCTGCA[C/T]CAGTTTCCCGAGTAG	80013
rs759242832	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15804640	AGTCCCTCCAATAAA[C/T]AAATAAAAGGTAAAT	80013
rs759322155	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15849889	AGTCATCTATATATG[C/G]CCTGTTTCAATTTTC	80013
rs759325130	snp	G/T	2.22502e-05	0.00333535	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	FAM188A	GRCh38.p7	10:15778967	CATCTGTTATTAAGA[G/T]CTTCCTTATAAATAC	80013
rs759358472	snp	A/C			upstream-variant-2KB	FAM188A	GRCh38.p7	10:15861361	AATAGTTAAGAGGCC[A/C]AGCTGTGGGTCATAC	80013
rs759375490	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15840619	AAAGATGATAGTTAA[C/T]GTGATGCTCTGTGGG	80013
rs759400392	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15850726	CAATTCTAATTTTGC[C/T]CTGGTCCTGTGATCT	80013
rs759476856	snp	A/T	0.000234165	0.0108179	intron-variant, missense	FAM188A	GRCh38.p7	10:15837555	ACTTGGCAGGGAACC[A/T]CTTCATCTCTTAGGT	80013
rs759506771	snp	A/C/G	6.64103e-05	0.00576206	synonymous-codon, downstream-variant-500B, nc-transcript-variant	FAM188A	GRCh38.p7	10:15779070	CAGACAGCGTTTAAT[A/C/G]GGAGTGTCATCTGTC	80013
rs759526382	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15838725	TATAAAAAGGCATAA[C/T]ACTTTCAAACTACAC	80013
rs759536016	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15796743	GAAACACCCTAGAGG[A/G]CAGAAATTTCTTTCC	80013
rs759566654	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15835065	AATTTGCGTTTTAAT[C/T]ATTTAACTGGTACAT	80013
rs759576796	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15808874	CACTGATCTTCTGAA[A/G]ATGAAACTAGATGCT	80013
rs759658065	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15817561	AAAAACTTGAGAACA[C/T]GATTGTGTGTGTGTG	80013
rs759681075	snp	C/T	0.000117158	0.00765279	intron-variant, utr-variant-5-prime	FAM188A	GRCh38.p7	10:15837565	GAACCTCTTCATCTC[C/T]TAGGTGAACTGTCTG	80013
rs759683062	snp	A/C	1.75385e-05	0.00296124	intron-variant	FAM188A	GRCh38.p7	10:15789204	TCTTAAACTTAATCG[A/C]ATCTTTTTGAGTTGG	80013
rs759692936	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15805867	CCAACATGTAAGTTA[C/T]GAGGGCGGTAAGCTT	80013
rs759701593	snp	C/T	1.67405e-05	0.00289309	utr-variant-5-prime, missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15837313	AAACTTCTGAACGAT[C/T]TTTTTCTGGGGGAAA	80013
rs759708324	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15830221	AAATTTCTCCCAGTT[A/C]ATTGTGATGTGCAGA	80013
rs759776973	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15809772	ACATAGGGTGGCTTA[C/G]ATGCATTTCTCACAA	80013
rs759850273	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15795402	AAGTAAAGATAACTG[A/G]ATCCATTCAGATATC	80013
rs759856142	in-del	-/CTAT			intron-variant	FAM188A	GRCh38.p7	10:15804271	AAGCTGTTAATGGGA[-/CTAT]CTATCTAATAGCCTA	80013
rs759884045	snp	A/G/T	0.000135912	0.00824252	intron-variant	FAM188A	GRCh38.p7	10:15789329	CATTATCTAGGGGGG[A/G/T]AAAAATCAGAAACAA	80013
rs759901673	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15794024	GCACAGTGTTAACAG[A/C]GTGACTGCAAATCCA	80013
rs759910330	snp	C/G	1.64912e-05	0.00287147	utr-variant-5-prime, missense, intron-variant, nc-transcript-variant	FAM188A	GRCh38.p7	10:15847869	TCTATGTTACCTGAA[C/G]AGGTGCAATAACAGC	80013
rs759928581	in-del	-/ATTT			intron-variant	FAM188A	GRCh38.p7	10:15799202	CCCAAATGCTCTAAC[-/ATTT]ATTTATTTTTTTTAG	80013
rs760018087	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15853776	TTTTACCTAGTATAA[C/G]TACCAATAAGCTACA	80013
rs760018868	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15823806	CCCACCGCCTGCCAC[C/T]GACCCTTCCCAGTCT	80013
rs760037047	snp	C/T	1.65157e-05	0.0028736	missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15833680	TTAGAAACAGCATGT[C/T]CCGTCAGCAGGAGAT	80013
rs760088852	snp	A/C	1.69355e-05	0.00290989	missense, downstream-variant-500B, nc-transcript-variant	FAM188A	GRCh38.p7	10:15782218	AAAAGATTCTGGACC[A/C]CTGGAGCCCTATTAT	80013
rs760106017	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15853073	GGATCCTTGAACCCA[C/T]TACCCCTCGAACACC	80013
rs760107264	snp	A/G	3.97007e-05	0.00445519	intron-variant	FAM188A	GRCh38.p7	10:15833757	GAATATAGTTGCCAA[A/G]TCAAATAATTCCTAC	80013
rs760126553	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15852915	TCATTCCCTAAACAA[C/T]ACAATGTAACAACTA	80013
rs760249144	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15828223	GGTATATTTGTGCAA[C/T]GGTATGTTATTCATC	80013
rs760252320	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15843439	GACAGGAACTGTGCA[A/G]TTATTTATTCAGAGT	80013
rs760271099	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15823981	CAAATAACAGGATTT[C/T]ATTCTTTGTTATTGT	80013
rs760283525	snp	A/G	4.3903e-05	0.00468504	intron-variant	FAM188A	GRCh38.p7	10:15841386	TTCATTAAAACAAAG[A/G]AACAAGAAAAAAACT	80013
rs760331963	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15781098	ACTCATTCGCACATT[A/G]GAAAACAACATCCAA	80013
rs760361189	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15799854	ATACTTGGCACACTA[C/T]GAACACTCACTGTTA	80013
rs760457587	snp	A/G	3.30633e-05	0.00406578	synonymous-codon, intron-variant, nc-transcript-variant	FAM188A	GRCh38.p7	10:15816850	CTTGGCAAAAAATAC[A/G]GTGAGGTGAGTCTCA	80013
rs760467724	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15787897	TTTCATGGGCCATTC[G/T]GTATTACAGTTGTAA	80013
rs760475633	snp	A/G	3.31945e-05	0.00407383	utr-variant-5-prime, missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15841459	AACTAGACTCTGCAG[A/G]ACTCCCAGAAATACT	80013
rs760624053	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15807386	GTGGAAGGTTGGACC[A/C]GGAATGCTGAGCAAG	80013
rs760630041	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15808829	CCCAACTTCAATGAA[G/T]AGTTTAAATGGAGTA	80013
rs760653499	snp	A/G	1.6981e-05	0.00291379	intron-variant	FAM188A	GRCh38.p7	10:15816946	CAAAATAAAACAAAT[A/G]AACAAATTAAAAATT	80013
rs760670297	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15848848	ATCATTTCACCTGCT[C/T]GGGCCTCAGTGTTCT	80013
rs760721981	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15805106	TGCCATAATTATTAA[A/C]ATCATTAATGAGTGA	80013
rs760779729	snp	A/C	1.66668e-05	0.00288672	synonymous-codon, nc-transcript-variant	FAM188A	GRCh38.p7	10:15837225	CAGTAATACAGAATA[A/C]AGAAAAAGCAATACT	80013
rs760782274	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15828506	AACAACTCTGAGAAA[A/G]TATTTAAAATACTGA	80013
rs760831479	snp	C/T			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15779827	TGCAGTGGCAGTGAT[C/T]ACAGAAATATATACT	80013
rs760909643	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15792754	CCTGACATATAATTG[C/T]ACAAGGGGGAGGGGA	80013
rs760923304	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15816459	TTCAAAGGAGATGCT[A/G]TAATTAAAACATTTT	80013
rs760961209	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15847141	TATAACAGTTCTTTT[A/C]TAACACTTCCAAAGT	80013
rs760976202	in-del	-/A	0.000688729	0.0185443	intron-variant	FAM188A	GRCh38.p7	10:15816808	CTGATGTCATAACTT[-/A]AAAAAAAAATCCTGC	80013
rs760996203	in-del	-/AG			intron-variant	FAM188A	GRCh38.p7	10:15816286	AAAAAAAAATGAAAA[-/AG]AGAAAAAAAATAAAA	80013
rs761007508	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15813584	ATTAAGAACAGACCC[A/G]TATCTATTTTTGCTC	80013
rs761084713	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15848004	AGCAGCTAAAAGAAT[C/T]TTTCATGTACTTTGC	80013
rs761181974	snp	A/G			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15779670	AAACTTGCTATTATG[A/G]TATTAAATATTCCTG	80013
rs761208261	snp	C/T	6.60818e-05	0.00574774	intron-variant	FAM188A	GRCh38.p7	10:15843278	AAAGAAATGCCTTTA[C/T]ACAATTAAAGCAATA	80013
rs761212022	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15852047	ATTTTTCAGGTCTCA[A/G]TTTAGGTGTTAATTC	80013
rs761363267	in-del	-/TCTAAC			intron-variant	FAM188A	GRCh38.p7	10:15807029	TGGTACTCACTAGTA[-/TCTAAC]TTTGGAGATGTCATT	80013
rs761364165	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15798144	TGAAATGAGTTTTAA[A/G]ATACTGCTGGTAATT	80013
rs761396986	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15799679	TGACTTCATAGCACA[C/T]AGGGAAACTGAAAAA	80013
rs761405775	snp	G/T	1.65965e-05	0.00288062	missense, downstream-variant-500B, nc-transcript-variant	FAM188A	GRCh38.p7	10:15779080	TTAATAGGAGTGTCA[G/T]CTGTCTGTAGCATGG	80013
rs761405837	snp	A/T	1.65056e-05	0.00287272	missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15833666	CACCATCCCATACAT[A/T]AGAAACAGCATGTCC	80013
rs761422217	snp	A/T	1.72886e-05	0.00294007	intron-variant	FAM188A	GRCh38.p7	10:15821763	ACAAAAAACGAAAAC[A/T]TAGCATTGTAGTAGT	80013
rs761474455	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15800624	AACCCATATGAAGTG[A/C]CACTAGTGATGCCGG	80013
rs761481345	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15795109	GAATGTTCATAGTTA[C/T]ACTGGGTTAAGAATA	80013
rs761483392	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15831721	CGCTCTATTGCTCAG[A/G]CTGGAGTGCCGTGGC	80013
rs761504396	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15852671	AATCATGTCATTGGG[A/T]ATACTAAAAATATAA	80013
rs761569348	snp	A/G	1.69631e-05	0.00291226	intron-variant	FAM188A	GRCh38.p7	10:15838325	ACATGGCAAATAAAT[A/G]ACACAAGATACACAC	80013
rs761571400	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15828727	AAAAATGGAAACAAT[A/C]TAACTGTTTACCATA	80013
rs761607475	snp	A/G	1.64923e-05	0.00287156	synonymous-codon, nc-transcript-variant	FAM188A	GRCh38.p7	10:15796143	TCTGGCTTGTTCTGA[A/G]GGAGCTTCAGGGGCA	80013
rs761607721	snp	A/C	1.82737e-05	0.00302267	intron-variant, downstream-variant-500B	FAM188A	GRCh38.p7	10:15782104	GTTACATACTCACAT[A/C]ATTATTTCATCAACC	80013
rs761629034	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15786876	ATTTAAATTGTGATG[A/C]CTTTGGAATATTGTT	80013
rs761631912	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15787718	GTCTAGTATTGGCCC[C/T]GTGAGATACTTTTGT	80013
rs761657533	snp	A/G	1.7383e-05	0.00294808	intron-variant	FAM188A	GRCh38.p7	10:15838198	ATGTGTCCACAGAGT[A/G]AGTATTTTAAATGTT	80013
rs761714710	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15848198	GGAGGATAAAGTATG[C/G]ACTTTAGTAAAATGA	80013
rs761718485	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15858926	AGGTAACTGACATAA[C/T]TGAATGTGAAAAAAA	80013
rs761737498	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15858471	CACTTTTTAAAATAA[A/T]ATAAAAACAGCTACC	80013
rs761756630	snp	A/G			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15783019	CCCCTTGTCTTCCTG[A/G]CCATATCCGATGGAT	80013
rs761780833	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15838531	TTCAGTTCAGCTATG[C/T]TACGGCAGTTATAAA	80013
rs761811762	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15795542	TAGCTATAATAAAGT[C/G]TTAACCGTTACCTAA	80013
rs761845131	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15838494	ATAATACTGAGAATA[G/T]AGAAGGGTGATTAAA	80013
rs761855308	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15830293	AGCAGTGGCAAACAT[G/T]TATTGAACAGTGCTC	80013
rs761901731	snp	G/T	1.65037e-05	0.00287256	utr-variant-5-prime, nc-transcript-variant	FAM188A	GRCh38.p7	10:15860300	AGTCAGTTCGGACAT[G/T]ATGAGGAACCGGCGG	80013
rs761913236	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15796540	ATTTTTTCCACATTT[C/T]TTTGTTCAGGTAAGA	80013
rs761931752	snp	A/G	3.94252e-05	0.00443971	intron-variant	FAM188A	GRCh38.p7	10:15860200	GTGAGAGCCCCGCCA[A/G]GGTACCTTGCGTCCA	80013
rs761940389	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15828165	AGCATTACTCATAAT[A/G]GCCAAGTGGAAACAC	80013
rs761960087	snp	A/C	1.65971e-05	0.00288067	intron-variant	FAM188A	GRCh38.p7	10:15816819	AACTTAAAAAAAAAT[A/C]CTGCTATAAGCATAC	80013
rs762015557	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15835255	AAGTTCTACATACTG[C/G]ATAAGTACAAGAAGA	80013
rs762067075	in-del	-/AT			intron-variant	FAM188A	GRCh38.p7	10:15781119	AACATCCAAGTTTGC[-/AT]ATATATATATACATG	80013
rs762096165	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15854921	AAGAGATGAAATCTT[C/G]ACTGTTTGGCCAGCT	80013
rs762101990	snp	C/G	5.18605e-05	0.00509191	intron-variant	FAM188A	GRCh38.p7	10:15837180	CATTAATCAAAGGCA[C/G]AAAAATCATCTTCTT	80013
rs762131560	snp	C/T			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15783223	GCACTTTCCCGGTGC[C/T]TGCTTCTTCAATTCA	80013
rs762151041	snp	A/C			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15784932	CTGCTATAGGATGGG[A/C]ACAGATGGGAATAGG	80013
rs762162882	snp	A/G	1.6563e-05	0.00287771	synonymous-codon, intron-variant, nc-transcript-variant	FAM188A	GRCh38.p7	10:15786621	TCCTAATCCTTCTGG[A/G]TCTAATTTATTCTTC	80013
rs762218686	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15856259	TATTAACTCCTAATA[C/T]ATTTTATATTTATAT	80013
rs762288976	in-del	-/CTT	2.34069e-05	0.00342095	cds-indel, downstream-variant-500B, nc-transcript-variant	FAM188A	GRCh38.p7	10:15778942	TGCCAGTCTTGACTC[-/CTT]CTTTCAACATCTGTT	80013
rs762323705	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15803996	TCAGTAGGAAGAGAT[A/C]CTACACATGAGACTC	80013
rs762326821	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15790673	TGGAGTCTCCCTCAT[C/T]CAAAATGCCTGGGTC	80013
rs762342863	snp	C/T	1.69209e-05	0.00290864	intron-variant	FAM188A	GRCh38.p7	10:15821612	ATCCACAATAGTGGA[C/T]ATCTAAACAAAAAAC	80013
rs762358852	snp	A/G	6.88444e-05	0.00586664	intron-variant	FAM188A	GRCh38.p7	10:15786700	GGAAAAAAAAAAGCT[A/G]CTTTTCTTTCATGAT	80013
rs762388946	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15846974	GTGATCCACCCACCT[C/T]GGCCTCCCAAAGTGG	80013
rs762396647	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15790996	ACAATGTGACCTTCT[C/T]AACAACATGCTTATA	80013
rs762441379	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15809002	CTTCCATTTTATACA[C/T]TCTAAATTCTAGTAA	80013
rs762486275	snp	A/G			utr-variant-3-prime, nc-transcript-variant	FAM188A	GRCh38.p7	10:15778359	CAGTAAAAGTTAACA[A/G]TGTTGACTATCAGAT	80013
rs762487760	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15832886	ACTATTATTTTCTCA[A/G]TTATATTTGCTCTGT	80013
rs762545278	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15802539	TCGCCTCCCACCAGG[C/T]CCCTCCTTACTATGC	80013
rs762591088	in-del	-/TA			intron-variant	FAM188A	GRCh38.p7	10:15781402	CTAATACATATATAT[-/TA]TATATATATATATAT	80013
rs762592694	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15822197	ACATGGACATTTAAT[A/G]CCATCCCTCTTTCCT	80013
rs762612760	snp	C/T	1.72829e-05	0.00293959	intron-variant	FAM188A	GRCh38.p7	10:15841638	TATAATGGTTTCCTC[C/T]GGAAAAAAAAAAATT	80013
rs762612796	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15802840	CATGTTTTGCTCTTT[C/T]GGTCTCAGTCATATA	80013
rs762621064	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15848926	TCCATTAATTGTTAC[C/T]ATTCAGACATTCAGC	80013
rs762632872	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15834370	TAAAATGAAATTAAC[A/G]TTTCATACATCAAGC	80013
rs762632940	in-del	-/TTTAAG			intron-variant	FAM188A	GRCh38.p7	10:15838756	AGGTTCAATGACAGC[-/TTTAAG]TTTGTTTCCTCATTT	80013
rs762645008	snp	A/C	1.6786e-05	0.00289702	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15779177	ACCAAGGTCAAGCAA[A/C]AGTCTTAGCAAATTC	80013
rs762747490	snp	A/G	1.74248e-05	0.00295163	intron-variant	FAM188A	GRCh38.p7	10:15838195	GCAATGTGTCCACAG[A/G]GTAAGTATTTTAAAT	80013
rs762764261	snp	A/T			upstream-variant-2KB	FAM188A	GRCh38.p7	10:15861537	CTTCCTAGCACATGG[A/T]AGGCATTTATGCAAC	80013
rs762765390	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15840749	CTCTTAACTAGCTTC[C/T]GTACCACTAGCTGTC	80013
rs762772044	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15856926	CTGCTGCCATTGTCT[C/G]TTATCTGATCTTGCT	80013
rs762793914	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15799893	CGAGCTTCTCGTGAG[C/G]TATTAGAAATAGAAT	80013
rs762794375	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15829336	GGTTCTTAACCCTGA[C/T]TACACAATATCACTT	80013
rs762814699	snp	C/G	3.32005e-05	0.00407421	missense, downstream-variant-500B, nc-transcript-variant	FAM188A	GRCh38.p7	10:15779074	CAGCGTTTAATAGGA[C/G]TGTCATCTGTCTGTA	80013
rs762872006	snp	A/G			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15779577	GAATATAGCTATTAT[A/G]TTCTGAGGAACATGT	80013
rs762927471	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15809469	GAAAGTGCCATGATA[C/T]GATTTCTGAAGACCC	80013
rs762981562	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15848752	ACCAGCATTGACTGA[C/T]AGCAGCTAGCGGAAG	80013
rs762992361	snp	C/T			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15779588	TTATGTTCTGAGGAA[C/T]ATGTGTCTCCTTCTA	80013
rs762995518	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15806051	ACACACTCCTCCTAC[C/T]CACAGGATGGGCTGT	80013
rs763020191	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15842364	GACACTTATGACAAT[A/G]CTTTACAAATGTTTT	80013
rs763073262	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15838054	TCAGCATAGTTTATA[C/T]ATTTACAAACTATTT	80013
rs763110444	snp	C/T	1.68878e-05	0.00290579	intron-variant	FAM188A	GRCh38.p7	10:15838313	TTTCAGCACTACACA[C/T]GGCAAATAAATGACA	80013
rs763121345	snp	C/T	6.59587e-05	0.00574239	utr-variant-5-prime, missense, intron-variant, nc-transcript-variant	FAM188A	GRCh38.p7	10:15847881	GAACAGGTGCAATAA[C/T]AGCACAGGGGCCACC	80013
rs763125669	snp	A/G	6.59587e-05	0.00574239	synonymous-codon, nc-transcript-variant	FAM188A	GRCh38.p7	10:15796131	TTGAAAAACTCTTCT[A/G]GCTTGTTCTGAAGGA	80013
rs763125934	snp	A/G	1.69861e-05	0.00291424	intron-variant	FAM188A	GRCh38.p7	10:15789337	AGGGGGGAAAAAATC[A/G]GAAACAACTTGAAAT	80013
rs763132988	in-del	-/TA			intron-variant	FAM188A	GRCh38.p7	10:15781171	AAAATTTGGATGCTG[-/TA]TATATATATCTTTGG	80013
rs763167782	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15805655	CTTCCTTGCCTCATT[A/G]ACATCAGATTCAGCC	80013
rs763200860	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15794296	TCCTGAAACAAAAGC[A/G]TATCATTTGGGGAAA	80013
rs763249875	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15836577	AACTGAGACTAACAC[A/G]TTACTAGAGCTATGA	80013
rs763253082	snp	C/T			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15783984	GTTAGACAGACTATA[C/T]TGGATTTCTGAATCA	80013
rs763260414	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15838897	CTTTACTAAGTGCCA[A/G]GCCCTTTTCTAAATG	80013
rs763296293	snp	A/G	1.67061e-05	0.00289011	intron-variant	FAM188A	GRCh38.p7	10:15834504	AAGTTTCTAAAAACT[A/G]GAGTTCACATGAGGA	80013
rs763319966	snp	A/G	0.00014118	0.00840059	intron-variant	FAM188A	GRCh38.p7	10:15860190	GGCTGCAAGTGTGAG[A/G]GCCCCGCCAGGGTAC	80013
rs763363715	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15788234	TACTATCATACCATT[A/T]GTTGGACTAGTTCAA	80013
rs763464660	in-del	-/TG			intron-variant	FAM188A	GRCh38.p7	10:15804947	TGTGAGGCACCAATC[-/TG]TGTCGTATGGGCAGA	80013
rs763491590	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15801867	TTCAAGATAAAGATC[C/T]TGGAGAAATTCAAGA	80013
rs763491734	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15816086	GCCTGGCCAACATGG[C/T]GAAACTGTCTCTACT	80013
rs763502607	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15846028	AGGTTTCACCACATT[A/G]GCCAGGCTGGTCTCC	80013
rs763520957	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15854801	AAAATAGGACAAATG[C/G]AGAACTGGAATAGAG	80013
rs763534232	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15821402	TCTGTGGCTTTTTTG[A/T]ATTATTTTGTACTGG	80013
rs763558370	in-del	-/AAAAC			intron-variant	FAM188A	GRCh38.p7	10:15795037	AAAATCTTCACTAGT[-/AAAAC]AAAACACAACACAAC	80013
rs763561663	snp	G/T	5.21417e-05	0.0051057	intron-variant, downstream-variant-500B	FAM188A	GRCh38.p7	10:15782231	CCACTGGAGCCCTAT[G/T]ATAAATAAAGGACTA	80013
rs763585188	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15821412	TTTTGAATTATTTTG[C/T]ACTGGGTTCTGCCCC	80013
rs763598271	snp	A/T	1.65999e-05	0.00288091	missense, downstream-variant-500B, nc-transcript-variant	FAM188A	GRCh38.p7	10:15779075	AGCGTTTAATAGGAG[A/T]GTCATCTGTCTGTAG	80013
rs763627311	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15790743	ATATTTGCAAATATA[C/T]AATGGCTGAACATCC	80013
rs763653160	in-del	-/A			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15780401	CTTTTCAGTCCCCAA[-/A]GCAAAACTGCCTTCT	80013
rs763687303	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15850197	TAATCTCTTAATCCC[A/G]TCATCTTCGTAAGCT	80013
rs763728912	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15828804	AACATGAGACATACA[C/T]TCATTCAGCATTTAC	80013
rs763758107	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15796953	TAGCTTTTACCTATA[A/G]TTGTCTTTGCCTATA	80013
rs763797292	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15822273	AGAAAATGATCTCTG[A/C]CTTAGAAAGGCTATG	80013
rs763874114	snp	A/G	3.44554e-05	0.00415049	intron-variant	FAM188A	GRCh38.p7	10:15821757	ACAACAACAAAAAAC[A/G]AAAACTTAGCATTGT	80013
rs763882053	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15850887	CACCCAGCTTTAAAA[A/C]TTCTCTCTTTTGTAC	80013
rs763903762	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15855242	GTGTTAACTGATAAC[A/G]GACAAAGGCTAGTAG	80013
rs763914822	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15841982	CTGTTGAAACCTCTA[C/T]TTTTTTTCCCTCACA	80013
rs763933959	in-del	-/AA			intron-variant	FAM188A	GRCh38.p7	10:15828577	CAATAAAGCTATAAG[-/AA]TAAAAAAAAAAAAAA	80013
rs764002591	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15840854	TTTTATGAATAATGA[A/G]AATAGCTATTATTTA	80013
rs764059363	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15817713	TTAGCAATACAATTT[A/G]CTGCATTTTCCTTTT	80013
rs764061938	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15786712	GCTGCTTTTCTTTCA[A/T]GATTAAATTACTGGT	80013
rs764077041	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15836622	GAAAAAGAGTAGGAC[C/T]AGAAGGGGACATATT	80013
rs764082200	snp	C/G	1.71852e-05	0.00293127	intron-variant	FAM188A	GRCh38.p7	10:15789355	AACAACTTGAAATAA[C/G]AATTTACTTCAAGAA	80013
rs764100321	snp	C/G	1.74178e-05	0.00295103	intron-variant	FAM188A	GRCh38.p7	10:15838196	CAATGTGTCCACAGA[C/G]TAAGTATTTTAAATG	80013
rs764111269	in-del	-/AGAT			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15783126	TCAGCTCCTACAGAA[-/AGAT]AGGCTGTGAGAATGT	80013
rs764122413	snp	C/T	8.2445e-05	0.00641995	synonymous-codon, nc-transcript-variant	FAM188A	GRCh38.p7	10:15796134	AAAAACTCTTCTGGC[C/T]TGTTCTGAAGGAGCT	80013
rs764131845	in-del	-/TTAAG			intron-variant	FAM188A	GRCh38.p7	10:15839288	AGCAGTCCAAATGTA[-/TTAAG]TTATTTCTTGGTTTA	80013
rs764168292	in-del	-/AA	0.000163282	0.00903406	intron-variant	FAM188A	GRCh38.p7	10:15841641	AATGGTTTCCTCTGG[-/AA]AAAAAAAAATTCTGT	80013
rs764191056	snp	A/G			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15785415	CAAATTAAATTAAAA[A/G]CAGGAATATTCTTTT	80013
rs764209201	in-del	-/A			intron-variant	FAM188A	GRCh38.p7	10:15835185	GTGCCTTCTTTTCTT[-/A]AAAAACCAATTTCCT	80013
rs764254807	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15835460	AAACAAAGAAGCATG[A/G]GCTCTTGCATATGCC	80013
rs764273748	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15825742	GAAATATGTATACAC[C/T]GTAGAATGGCTAAAC	80013
rs764282543	snp	C/T	3.31279e-05	0.00406975	missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15833695	CCCGTCAGCAGGAGA[C/T]TAATTAAACTTTGGC	80013
rs764302659	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15780993	GGATAATATTTGACC[C/T]ATCTTGCAGGGATTG	80013
rs764303186	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15832765	ACTGATTTTTTCCTT[A/G]ATATTATGCCCTTTC	80013
rs764304591	snp	C/T	1.64936e-05	0.00287168	utr-variant-5-prime, missense, intron-variant, nc-transcript-variant	FAM188A	GRCh38.p7	10:15847893	TAACAGCACAGGGGC[C/T]ACCTTCAAACTGTTC	80013
rs764362809	snp	C/T	4.33698e-05	0.0046565	intron-variant	FAM188A	GRCh38.p7	10:15860195	CAAGTGTGAGAGCCC[C/T]GCCAGGGTACCTTGC	80013
rs764363378	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15854860	AGTGACAACTAAGGT[G/T]TCTGGTTATGTTAAA	80013
rs764366193	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15781875	GACTAACTACGATGT[C/T]GATTTAGAAACACGC	80013
rs764457435	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15789563	CTCCGACGAAAGCTT[A/C]AAGTCAAATTACTTG	80013
rs764478744	snp	A/C	1.66643e-05	0.0028865	intron-variant	FAM188A	GRCh38.p7	10:15834511	TAAAAACTGGAGTTC[A/C]CATGAGGAGACAAGA	80013
rs764514131	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15845145	TATTCCAAGGATACA[G/T]TTGATATATGGTACA	80013
rs764531471	snp	C/T	1.65392e-05	0.00287564	missense, intron-variant, nc-transcript-variant	FAM188A	GRCh38.p7	10:15786602	ATGGGCCCAATAATA[C/T]GATTCCTAATCCTTC	80013
rs764556987	snp	G/T	3.61696e-05	0.00425247	intron-variant, downstream-variant-500B	FAM188A	GRCh38.p7	10:15782123	ATTTCATCAACCCAG[G/T]TGAACACCGACGACT	80013
rs764557863	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15846111	TACAGGCATGAGCCA[A/C]CACGCCTGGCCGTGA	80013
rs764563547	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15814071	AAGGAATGGCCGAAT[A/G]ATGATTCTTGTTATA	80013
rs764590281	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15814267	AGGGGAAAAAACAAC[C/T]CTTCACTGGGAACTC	80013
rs764624935	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15788164	TTTTGTAAATTAGAG[C/T]AGTGTAAACAACATG	80013
rs764656456	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15831752	ATGATCTCAGCTCAC[G/T]GCAACCTCCGCCTCC	80013
rs764730854	in-del	-/G	3.35897e-05	0.00409802	splice-acceptor-variant	FAM188A	GRCh38.p7	10:15837320	GAACGATCTTTTTCT[-/G]GGGGGAAAAAAAGAA	80013
rs764745860	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15844883	ATTTTTACTTTCCTG[A/G]CTTCCTAGTGAGGGT	80013
rs764760486	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15801820	TTGTGCATGAGTTCA[C/T]AGGATTTACAGAGCC	80013
rs764767328	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15802012	CAAACTGACATTCAT[C/T]ATAATTTTAACATAT	80013
rs764816130	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15859384	TTATGTTTTAACCTC[A/G]TCATCATCTTTCCTA	80013
rs764874870	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15799698	GAAACTGAAAAAGGT[A/G]AACAGGACTGAGAAC	80013
rs764888328	snp	G/T	0.000841302	0.0204925	utr-variant-5-prime, nc-transcript-variant	FAM188A	GRCh38.p7	10:15860328	CGGGCGGATCTTCGC[G/T]TTGCGGACTCCTGCC	80013
rs764888514	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15808904	TATAGGCAGGGTCCA[A/G]CTATTTTTATACTGG	80013
rs764926218	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15832772	TTTTCCTTAATATTA[C/T]GCCCTTTCATGTTTC	80013
rs764933361	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15838955	TCATATAAACCCTCT[C/T]AGCTCCATTTTACAG	80013
rs764951094	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15807544	TTTGTACTCTGCTAT[C/T]AACTCTACTGGCTAT	80013
rs764959765	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15849965	ATGAGTGAATGTTGC[A/G]GGAAGTTAGGGACCC	80013
rs764961159	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15795146	TTACCTTGGACAACT[A/G]CTTGTACCACTGGGC	80013
rs764997811	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15820131	TATTCCTATTAAATA[C/T]TGTGGAAAAGAATAT	80013
rs765078484	snp	C/T	2.10316e-05	0.00324274	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	FAM188A	GRCh38.p7	10:15778976	TTAAGATCTTCCTTA[C/T]AAATACTTAGACAAA	80013
rs765104426	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15795867	TCAAGATTAATCAGA[A/G]GGGTCAACTACACCT	80013
rs765175244	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15818633	ATTGGTTTAACATAC[A/G]AAAGAATATTATTTG	80013
rs765212818	snp	C/T			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15784103	AGCTACTAAGATACC[C/T]AGTGTATGACCTTCA	80013
rs765225884	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15848120	AGAACCTATCCACCC[C/T]CACTCCCAAATGCAC	80013
rs765251866	snp	G/T	1.67598e-05	0.00289476	utr-variant-5-prime, missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15837316	CTTCTGAACGATCTT[G/T]TTCTGGGGGAAAAAA	80013
rs765265234	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15840647	GGGTAGAATAAGTCA[C/G]TTATTTAACATAAGC	80013
rs765317581	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15858023	AGCAAAGCAGTGTCT[C/T]GTGCCTGTTCCCACA	80013
rs765321979	snp	C/T			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15780287	AAAGTGCTAAAGATA[C/T]ATTGTAACGTGAAAT	80013
rs765335544	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15796905	TTGACACACATGAAT[C/G]TAAAATGTAGGCTCC	80013
rs765368968	in-del	-/AA			intron-variant	FAM188A	GRCh38.p7	10:15835449	CCCGCAGGGGGAAAC[-/AA]AGAAGCATGAGCTCT	80013
rs765391141	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15794110	AAAGATATAAAAATA[C/T]TCCTGGGTACCTTCA	80013
rs765402229	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15838568	AAAATTACTGATAAT[C/T]AGTGCCTCACATATC	80013
rs765415842	in-del	-/TA			intron-variant	FAM188A	GRCh38.p7	10:15781172	AATTTGGATGCTGTA[-/TA]TATATATATCTTTGG	80013
rs765423350	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15835411	ATTAATTAACAACCA[A/G]GATTTTTAAAGAATG	80013
rs765443491	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15803166	TGTTCAGAGATGTAA[C/T]CAGAAAGTTATGAAA	80013
rs765443510	snp	C/G	0.00023571	0.0108535	intron-variant, utr-variant-5-prime	FAM188A	GRCh38.p7	10:15837587	AACTGTCTGGCATCA[C/G]TAAATTCTTCAATAA	80013
rs765445547	snp	G/T	1.73525e-05	0.0029455	intron-variant	FAM188A	GRCh38.p7	10:15789219	AATCTTTTTGAGTTG[G/T]CTAAATAACACTTCC	80013
rs765514194	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15793081	GAATTGTTGTTGTCC[A/G]GTATCTTTGATCATA	80013
rs765514403	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15805993	TCTCAAATTCCTTTT[G/T]GCCATCACCACGTGC	80013
rs765539415	in-del	-/A			intron-variant	FAM188A	GRCh38.p7	10:15851753	CCACACAGTTGCCAG[-/A]AAGTATTTTAGAAAT	80013
rs765577633	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15853081	GAACCCACTACCCCT[C/T]GAACACCAACAGACA	80013
rs765592152	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15823118	GTAGCCTTAACTACA[A/T]CATCTAGATGGTGTA	80013
rs765602879	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15781314	CCTTCCACAATTTAG[A/G]TACATGAAGTCAGCA	80013
rs765616117	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15800821	CCATACAAACCTTCC[A/G]CTTTTTGCAAAATAC	80013
rs765635014	snp	A/G	1.64895e-05	0.00287132	utr-variant-5-prime, synonymous-codon, intron-variant, nc-transcript-variant	FAM188A	GRCh38.p7	10:15847876	TACCTGAACAGGTGC[A/G]ATAACAGCACAGGGG	80013
rs765662765	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15836351	GATTCCATCTAATAG[C/G]TTCAGACAGAAGACC	80013
rs765705955	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15853786	TATAACTACCAATAA[A/G]CTACAGTTATTCAGA	80013
rs765723398	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15824324	CTGACTGGGGTAAGA[A/T]GACATCTCATTGTGG	80013
rs765847160	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15851433	TTAGATTCTGGGCAC[A/G]TTTTCTTTCAGGTCC	80013
rs765847756	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15804014	ACACATGAGACTCAA[C/T]GATTACATACTGTTT	80013
rs765853613	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15799877	CACTGTTAGCTAACT[A/G]CGAGCTTCTCGTGAG	80013
rs765884812	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15853000	AAGTGTAGGGGAAGT[C/T]GTGTGTAGGTTATAT	80013
rs765908963	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15813237	CTTCATCTTACACCT[A/T]GTCCCCCTAATTCTC	80013
rs765912646	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15843519	AATACATATTTTCTG[A/G]CAAGTAGAAGAACTA	80013
rs765918541	in-del	-/TCTT			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15786280	AGTGGAGAAAGAGAA[-/TCTT]TCTCTTTTTACTCCT	80013
rs765932558	snp	A/C/G	0.000165734	0.00910173	utr-variant-5-prime, missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15841467	TCTGCAGGACTCCCA[A/C/G]AAATACTAGCAGTTT	80013
rs765958539	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15788035	ATCTGATAAAACAAG[A/G]AAAATTAGGTAGATG	80013
rs765977882	snp	C/G	3.40837e-05	0.00412804	missense, downstream-variant-500B, nc-transcript-variant	FAM188A	GRCh38.p7	10:15782222	GATTCTGGACCACTG[C/G]AGCCCTATTATAAAT	80013
rs766001514	snp	C/G	1.65397e-05	0.00287569	intron-variant	FAM188A	GRCh38.p7	10:15796201	AAGCATGTTGTCAAC[C/G]AGCTACAGTATTATG	80013
rs766016039	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15791079	TCATAAGCACAGATA[A/T]TCTGAAGTGTAACCA	80013
rs766046506	in-del	-/AGGGAATTTTGGAGATTTCAAGTAAGAACCAACCTAGA	1.6524e-05	0.00287432	frameshift-variant, intron-variant, nc-transcript-variant	FAM188A	GRCh38.p7	10:15816882	GCCAACAATCCAAAT[lengthTooLong]AGGGAATTTTGGAGA	80013
rs766057949	snp	A/G	1.64993e-05	0.00287218	intron-variant	FAM188A	GRCh38.p7	10:15841388	CATTAAAACAAAGGA[A/G]CAAGAAAAAAACTTC	80013
rs766072082	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15848981	TCTGATATTATGCCA[A/G]TCATCTAGGATATAT	80013
rs766089065	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15800722	TGAGGTCTGCTGCTG[C/T]GGTTGCTCACTATGT	80013
rs766089200	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15787247	GTCCAGCAGCAGCCT[A/G]AAGTGCATACCAGCC	80013
rs766092027	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15859164	ATTGTAATTTTACCA[A/G]CTCTTAAAACAAACA	80013
rs766107168	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15830476	AACCACAGTAGTCTA[A/G]TTCCACACAGCTAAC	80013
rs766121014	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15831599	TCTCAAGAACCGAAA[C/G]TGATAATTGACTAAT	80013
rs766128767	in-del	-/AGAG			intron-variant	FAM188A	GRCh38.p7	10:15819097	GTGCAGGAGGGAGAA[-/AGAG]ATTATTTCATCACCT	80013
rs766150233	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15802796	ACTAATACAACAAAC[A/T]GTGTCTTGAACAATA	80013
rs766186871	in-del	-/C			intron-variant	FAM188A	GRCh38.p7	10:15827024	CTTGAGAGACTGAGG[-/C]CAAGAGGACCACTGG	80013
rs766202097	snp	C/T	1.65241e-05	0.00287433	missense, intron-variant, nc-transcript-variant	FAM188A	GRCh38.p7	10:15816866	GTGAGGTGAGTCTCA[C/T]TGCCAACAATCCAAA	80013
rs766214715	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15832435	ATATTACCCAAGAGA[C/T]ACTGAAATGAGATTT	80013
rs766219619	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15806455	CAACCAATCCTACCT[C/T]GTTTTCTACAATTTT	80013
rs766309688	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15818926	ATGGTTGCATTGCAT[C/T]GTGAATATATTAAAA	80013
rs766377313	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15849760	TCTTCAATCTCTTCC[A/G]GGAAGCATATAAACA	80013
rs766417923	snp	C/G	8.77693e-05	0.00662397	utr-variant-5-prime, nc-transcript-variant	FAM188A	GRCh38.p7	10:15860314	TGATGAGGAACCGGC[C/G]GGCGGATCTTCGCTT	80013
rs766419407	snp	A/C	1.66363e-05	0.00288407	missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15837228	TAATACAGAATACAG[A/C]AAAAGCAATACTCCA	80013
rs766457670	in-del	-/A			intron-variant	FAM188A	GRCh38.p7	10:15841230	TGCATTTTTTTTTGC[-/A]AAAAATGTAGTATCT	80013
rs766464383	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15791341	ATCTGACATTTCACC[A/C]ACTGACTCCCTAGAG	80013
rs766565386	snp	A/C/G	0.000105558	0.00726424	intron-variant	FAM188A	GRCh38.p7	10:15789203	GTCTTAAACTTAATC[A/C/G]AATCTTTTTGAGTTG	80013
rs766575325	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15803160	TTTAAATGTTCAGAG[A/G]TGTAATCAGAAAGTT	80013
rs766600555	snp	A/G			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15785172	CGTGGGAGGCAAACA[A/G]CATGAACTATACAGA	80013
rs766674603	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15839693	AAAGAACAGGTAAAA[C/T]AGATTGTTACACGGA	80013
rs766716939	snp	C/T	1.65573e-05	0.00287721	intron-variant	FAM188A	GRCh38.p7	10:15843162	TAATTTTAGATCATC[C/T]CTATTAAAACAGAGG	80013
rs766732675	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15781109	CATTAGAAAACAACA[C/T]CCAAGTTTGCATATA	80013
rs766780616	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15835297	TAACCTCATCAATTC[C/T]AGAAGGACAAAGATA	80013
rs766804054	snp	C/T	1.65244e-05	0.00287436	intron-variant	FAM188A	GRCh38.p7	10:15843280	AGAAATGCCTTTACA[C/T]AATTAAAGCAATAAT	80013
rs766828335	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15852096	TACAAACCTATCTAA[A/G]TAGTCTCTCCTGTCA	80013
rs766852074	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15823540	TTATTAAAAATGTTA[C/T]TTATGTTAATATTAA	80013
rs766867692	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15848011	AAAAGAATCTTTCAT[A/G]TACTTTGCTTTGAGA	80013
rs766900355	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15788535	CATTCTTAGAAAAAC[C/T]TGCAGAAGGAAAAAC	80013
rs766950237	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15850960	TAGAAAAGAACCTAC[A/G]TTGAAATATTGGGTG	80013
rs766966811	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15822429	TGAATCTTGAAGCGT[A/G]TTACAGTTCTCCAGG	80013
rs766978919	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15823304	CACAAGACCCTCTTA[C/G]AGACTACGTGAGATC	80013
rs766981926	snp	C/T	8.73721e-05	0.00660897	intron-variant	FAM188A	GRCh38.p7	10:15821769	AACGAAAACTTAGCA[C/T]TGTAGTAGTGTGTAT	80013
rs766990186	snp	C/G			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15784712	ACTGCACTCCAGCCT[C/G]GGTAAAGGAGCGAAA	80013
rs767039717	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15852005	TAAAAATGCTCTTTC[C/T]GCTACTCTCCATATA	80013
rs767055435	snp	A/G			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15779848	AATATATACTGGCAG[A/G]TGAATAGCAAGAAAA	80013
rs767074272	in-del	-/ATGAACA			intron-variant	FAM188A	GRCh38.p7	10:15818692	ATGTAAAAAACAGAG[-/ATGAACA]ATGAAAACACCATGC	80013
rs767090302	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15788770	GATATGCCATAATAT[A/G]TTGCAGCCATCCCTA	80013
rs767106323	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15799481	GGATTACAGGCTTGA[A/G]CCACTGCAACCAGCC	80013
rs767148052	snp	C/G			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15785706	CTTTTTGAATCTTAC[C/G]TCTTTCTTAACAATT	80013
rs767152768	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15817866	TTCTTATCACTAGGA[A/G]GGAAGTGGAAAATAG	80013
rs767157152	snp	C/T	1.70723e-05	0.00292162	intron-variant	FAM188A	GRCh38.p7	10:15838214	AGTATTTTAAATGTT[C/T]CAATGTTACTTACTG	80013
rs767159300	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15798227	TTACTTTTTTCTGGG[C/T]TAAATCTTTTTGGGG	80013
rs767177975	snp	C/T	1.65097e-05	0.00287308	missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15833677	ACATTAGAAACAGCA[C/T]GTCCCGTCAGCAGGA	80013
rs767224599	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15812027	GCTCACTGCAACCTC[C/T]GTCCCCTGGGTTCAA	80013
rs767274503	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15851773	ATTTTAGAAATGGAA[A/G]TCAGATTTTGACACA	80013
rs767300788	snp	C/T	1.8279e-05	0.00302311	intron-variant, downstream-variant-500B	FAM188A	GRCh38.p7	10:15782109	ATACTCACATAATTA[C/T]TTCATCAACCCAGTT	80013
rs767400655	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15858946	TGTGAAAAAAAAGAG[C/T]CCAAGTCATTACATG	80013
rs767435212	in-del	-/T			intron-variant	FAM188A	GRCh38.p7	10:15848502	AGCCAGGTGTGGTGG[-/T]GGGCAACTGTAGTCC	80013
rs767447094	snp	A/C	3.35385e-05	0.00409489	utr-variant-5-prime, synonymous-codon, nc-transcript-variant	FAM188A	GRCh38.p7	10:15860210	CGCCAGGGTACCTTG[A/C]GTCCAGCGGCAGAAA	80013
rs767460837	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15806112	GTACAGGACTGAAAT[A/G]TCAGGGTTGTTGGTT	80013
rs767465178	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15796696	CAATCAACTTCTACA[C/T]GTCCAGAATTTTAAT	80013
rs767472575	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15804952	GGCACCAATCTGTGT[C/T]GTATGGGCAGAGAAA	80013
rs767524013	snp	A/G	3.29957e-05	0.00406162	missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15796156	GAAGGAGCTTCAGGG[A/G]CAACTAAAGCCATAT	80013
rs767605752	snp	G/T			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15783088	CTGGAATTAAGGGAA[G/T]ACAGCTGCTGGCAAC	80013
rs767623885	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15818859	GGGACTGCTAATGGG[A/T]TTAGAGCTCCTTTTG	80013
rs767641295	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15834522	GTTCACATGAGGAGA[C/T]AAGAGATTTTAGTTA	80013
rs767682833	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15854079	TCACTGATGTATACT[C/G]TTATAAATTAATGCA	80013
rs767690266	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15814749	GTGTGCTGTTTGACA[A/C]ATGCGACAGCACAAT	80013
rs767717048	snp	A/G	8.53133e-05	0.00653065	intron-variant, downstream-variant-500B	FAM188A	GRCh38.p7	10:15782268	CTTTAAATTATATTT[A/G]TATCAGGCAATTTCT	80013
rs767723388	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15813563	TCAAGGAGAATGTCC[A/G]CCTCCATTAAGAACA	80013
rs767749162	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15816399	CCATCTTAAAAGAGC[A/C]TTTGACTTTAATACC	80013
rs767761905	in-del	-/TTA	2.29618e-05	0.00338827	cds-indel, downstream-variant-500B, nc-transcript-variant	FAM188A	GRCh38.p7	10:15778958	TTCTTTCAACATCTG[-/TTA]TTAAGATCTTCCTTA	80013
rs767767324	snp	A/C	0.000153784	0.00876747	intron-variant	FAM188A	GRCh38.p7	10:15837197	AAAATCATCTTCTTG[A/C]ACACACCTTTGTCAG	80013
rs767788662	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15828197	CCACATGTTGGCGAA[C/G]AAATGAATGTGGTAT	80013
rs767813083	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15809852	TTTGACAGAGACAGA[A/G]GGTTAGTAGGAAAAG	80013
rs767872721	snp	A/G			upstream-variant-2KB	FAM188A	GRCh38.p7	10:15861926	ATAGCATTCCTTTTG[A/G]TCTTTATTCCCTTTA	80013
rs767874326	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15802948	GAGGATGAAAAAAGA[C/G]AATAAAAAGAGAAAA	80013
rs767911740	snp	C/T	1.65748e-05	0.00287874	missense, intron-variant, nc-transcript-variant	FAM188A	GRCh38.p7	10:15786629	CTTCTGGATCTAATT[C/T]ATTCTTCATGAGATT	80013
rs767919295	snp	A/C/T			intron-variant	FAM188A	GRCh38.p7	10:15833044	GTGAAGGGAATTTTA[A/C/T]TCAGTTATGTATCAG	80013
rs768077823	snp	C/T			utr-variant-3-prime, nc-transcript-variant	FAM188A	GRCh38.p7	10:15778436	ATAAATGGTAATGGT[C/T]TCTTAGAGTTTCTAC	80013
rs768079988	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15792457	TGGCACTATACAGAA[A/C]ACTGTTAGCTGGGGA	80013
rs768116455	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15833937	TCACATACATTTAAC[A/G]ACTTTATCTAAGATA	80013
rs768125909	snp	C/T			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15779605	TGTGTCTCCTTCTAA[C/T]TTAAGTATTGAATTT	80013
rs768137225	snp	A/G	9.80825e-05	0.00700226	intron-variant	FAM188A	GRCh38.p7	10:15841641	AATGGTTTCCTCTGG[A/G]AAAAAAAAAATTCTG	80013
rs768141209	snp	C/T	6.61354e-05	0.00575007	utr-variant-5-prime, missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15841500	TCAGTTGTCTTTCCT[C/T]TTAACCATGAAACCA	80013
rs768243418	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15803903	AAATACACTTGCATT[C/T]TCTTTTCTTCATCCC	80013
rs768284949	in-del	-/A			intron-variant	FAM188A	GRCh38.p7	10:15859420	CTTTAGGAATGTGTC[-/A]AGTTGTTTGCCTATC	80013
rs768296083	in-del	-/G			upstream-variant-2KB	FAM188A	GRCh38.p7	10:15860910	CATAAGCTGGAGGCT[-/G]TCCGCCTCTGTACTT	80013
rs768314299	snp	A/G	1.69063e-05	0.00290738	synonymous-codon, downstream-variant-500B, nc-transcript-variant	FAM188A	GRCh38.p7	10:15782164	TCATACCTTTTCATT[A/G]TAATTTGACTGCTTC	80013
rs768355609	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15835085	AACTGGTACATAAAA[C/T]GGAAGGTTTACTTCT	80013
rs768357112	in-del	-/C			intron-variant	FAM188A	GRCh38.p7	10:15847392	TTTTATTCAGAAAAG[-/C]CAAAGCTATAGCATA	80013
rs768392145	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15824791	ATAATATCATGTTAC[A/T]AAATACAGCAAACTA	80013
rs768418357	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15800476	GAGCACAAGTATGGC[A/G]CTAATCATCTCCGCA	80013
rs768452403	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15811723	AGCCACTAATTTGCT[G/T]CAGGAAAAAAAATAA	80013
rs768458365	snp	A/G	4.95315e-05	0.00497627	intron-variant	FAM188A	GRCh38.p7	10:15847845	CCCTCTAAGGAGTTG[A/G]TAAAGGAGTCTATGT	80013
rs768465985	in-del	-/TTA			intron-variant	FAM188A	GRCh38.p7	10:15836909	CAGCTTCCAGAAGGG[-/TTA]GTTAAGGGGTCAAGT	80013
rs768478731	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15791934	ACTAGCTAAACTGGA[A/C]ACTGCAGGAAGAGAA	80013
rs768499208	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15852478	GTAAAACAAAAATAA[A/T]GAAGTTGGGAACTTT	80013
rs768516194	snp	C/T			intron-variant, missense	FAM188A	GRCh38.p7	10:15780932	CTGTGTGACCCTGGG[C/T]GAGTCACTTGATCTC	80013
rs768598294	in-del	-/AC	1.65045e-05	0.00287263	intron-variant	FAM188A	GRCh38.p7	10:15796072	ATATGAAGACATAAA[-/AC]ACAGAGATGATGTTA	80013
rs768644673	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15845075	TTTCTTAGTTTGGAA[A/G]TCTCTGTTTCTCTTA	80013
rs768696203	snp	A/G	1.65767e-05	0.00287891	intron-variant	FAM188A	GRCh38.p7	10:15816918	AGTAAGAACCAACCT[A/G]GAACAAATGTAGCAA	80013
rs768703748	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15799405	GGTTTCACTATCTTG[A/G]CCAGGCTGGTCTTGA	80013
rs768717057	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15809129	GTGACCCAAATAAAT[G/T]ATTCTTAAAACCCAA	80013
rs768717658	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15849529	ATAGAGATGATGCTG[A/C]CGTAATGAAAGCAAC	80013
rs768747251	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15809550	AGCTCAGATGACCTG[C/T]TTGGAAAGTTCTCCA	80013
rs768804318	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15790050	CCATTTACTCATTCC[C/T]GAAGATTGTCTCAGC	80013
rs768845489	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15828132	TCTCATAAAAACTTG[C/T]ACATGAATGTACCTC	80013
rs768933527	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15797436	CAACATTATTTTGCT[A/G]ATAATGTATACGCCC	80013
rs768949057	snp	A/C	1.66167e-05	0.00288237	intron-variant	FAM188A	GRCh38.p7	10:15816816	CATAACTTAAAAAAA[A/C]ATCCTGCTATAAGCA	80013
rs768953089	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15841204	CCAGAACATTTTTAA[A/T]AGTTTAAGAGATGCA	80013
rs768953615	snp	A/G	2.69582e-05	0.00367129	utr-variant-5-prime, missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15860289	ATCAGCTCTTTAGTC[A/G]GTTCGGACATGATGA	80013
rs768973875	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15838136	AGTAGCGCATTTCTA[C/T]GTAAAACTAAGAACC	80013
rs769038650	in-del	-/ATAA			intron-variant	FAM188A	GRCh38.p7	10:15822571	GTCTGGGGGGACATG[-/ATAA]ATAGTGATTAACACA	80013
rs769038763	snp	G/T			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15783989	ACAGACTATATTGGA[G/T]TTCTGAATCAGCTAC	80013
rs769040917	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15840093	TCACATCAATATACA[C/G]ACTGGCTTTAAGCAC	80013
rs769055952	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15802066	ACAGTATATAATACA[C/T]ATAAAATACAAAATA	80013
rs769097934	snp	A/T	1.65496e-05	0.00287655	utr-variant-5-prime, missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15837275	TTGAATACTGGTCCA[A/T]GACAGCATCTTTTAA	80013
rs769184460	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15817191	TAGCCCTAAGAGTCA[C/T]TCTCAGGTTTTGCTA	80013
rs769200007	in-del	-/C			intron-variant	FAM188A	GRCh38.p7	10:15817605	AAGTTTAATACTAAA[-/C]AAACAGAATAGACTT	80013
rs769202109	snp	G/T			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15784680	AGGCGGAGGTTACAG[G/T]GAGCTGAGATCGTGC	80013
rs769209393	snp	A/G			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15784574	ACAAGGTGAAACCCC[A/G]TCTCTACTAAGGATA	80013
rs769255179	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15804267	GGACCAAGCTGTTAA[C/T]GGGACTATCTAATAG	80013
rs769268709	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15790563	TAGCTAAAGGCTCAG[A/C]GTCTCCGAATGTGAA	80013
rs769273661	snp	A/C	1.66896e-05	0.00288869	missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15789272	CTGAAACAAGGTCCA[A/C]TGCTTTCATCACATC	80013
rs769276232	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15829070	AAAGCCTAGGCACCT[C/T]GTTTACAGAAGCAAG	80013
rs769336207	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15834134	ACTATCACTGTTTCA[C/T]TGAGTTTTGGTAAAA	80013
rs769340046	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15802525	CCCCCATGACTCAAT[C/T]GCCTCCCACCAGGTC	80013
rs769363791	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15786686	CAGTGGATACCAGAG[A/G]AAAAAAAAAAGCTGC	80013
rs769383451	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15815627	CAAGTTACCTATGAT[A/C]CCAGAGATGTTTAAC	80013
rs769404327	snp	A/C	1.8871e-05	0.00307166	intron-variant	FAM188A	GRCh38.p7	10:15833738	TTAAAAAGCAATTAA[A/C]TATGAATATAGTTGC	80013
rs769421224	in-del	-/A	0.000108189	0.00735409	intron-variant	FAM188A	GRCh38.p7	10:15841393	AAACAAAGGAACAAG[-/A]AAAAAACTTCAGGAA	80013
rs769427699	snp	C/T	4.94972e-05	0.00497455	utr-variant-5-prime, missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15843235	TCCCGCCAAGAAGAC[C/T]TCTCCGAAGAAAACA	80013
rs769446285	in-del	-/A			intron-variant, downstream-variant-500B	FAM188A	GRCh38.p7	10:15782348	GGGGACTCATTTGAC[-/A]AAAGAAGGAACTTAG	80013
rs769492536	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15846864	AAGTAGCTGGGACTA[C/T]AGGTGCCCACCACCA	80013
rs769555275	snp	A/C	1.6717e-05	0.00289106	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15779163	AACAAAATAAAGCCA[A/C]CAAGGTCAAGCAACA	80013
rs769602198	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15811234	AATAAAACCGAAGTT[C/G]AAATGTCAAAGATTT	80013
rs769643453	snp	C/T	3.3106e-05	0.0040684	intron-variant	FAM188A	GRCh38.p7	10:15833621	CAACATAACAAGGAA[C/T]ATACTTACTCATTCC	80013
rs769693500	snp	A/G	3.38221e-05	0.00411216	intron-variant	FAM188A	GRCh38.p7	10:15821750	AACAACAACAACAAC[A/G]AAAAACGAAAACTTA	80013
rs769715854	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15842274	TACAAGGAGGTTTCT[C/G]TCTCTCCTAATGGAT	80013
rs769726678	snp	C/G			upstream-variant-2KB	FAM188A	GRCh38.p7	10:15861440	TACCTAGGCTTTTTT[C/G]TTTCTAAAAGGGAGA	80013
rs769753113	snp	A/G	6.60666e-05	0.00574708	intron-variant	FAM188A	GRCh38.p7	10:15847841	ATGTCCCTCTAAGGA[A/G]TTGGTAAAGGAGTCT	80013
rs769768703	snp	C/T			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15779445	TTCAACGGATCTATA[C/T]CATCGGAAAGAAATG	80013
rs769771792	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15810051	AAGTAAAACTGACTT[A/G]TGAAAAATCTCTTTT	80013
rs769775963	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15815554	AGGAAAGCACATCAC[A/C]ATGAAGAAACCTCTA	80013
rs769797078	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15830250	GACAAGTTTGAGAAC[C/G]AGTTGTTGATAAGAG	80013
rs769829873	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15792985	TACAGATGAAAAACT[A/G]AGGTAGGAACTCGTC	80013
rs769860847	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15858902	TCTCCCTCTAAGAAG[A/C]CCAAGATTAGGTAAC	80013
rs769904239	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15851627	ATTTCCATCCCATCT[C/T]CAGTCCACCCTATAG	80013
rs770024792	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15787693	CTGCCTCACAGACCT[C/G]CTACCTGACGTCTAG	80013
rs770025158	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15843996	ACAGGTTACAATGAC[A/G]ACTTTTCCTCACCTG	80013
rs770066458	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15787869	TCATTTAATCCTTAG[C/G]ATGGCCCAGTTATTT	80013
rs770085438	snp	A/G	1.70136e-05	0.00291659	utr-variant-5-prime, missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15841428	AAATATATCTTACAA[A/G]AATGTTCCACTTGGC	80013
rs770086411	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15849415	TTAACCAGCAGAGAT[A/C]TTTCAGTAAAACAGT	80013
rs770106363	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15808182	AGTTGTTATTTTAAG[A/G]TCTTAAAAGTCACAG	80013
rs770110310	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15795408	AGATAACTGAATCCA[C/T]TCAGATATCTACAAG	80013
rs770154502	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15826359	CTGTTCTATTGGAGA[A/G]GCAAAAGATGGTTTC	80013
rs770159046	snp	C/T	1.67652e-05	0.00289522	intron-variant, utr-variant-5-prime	FAM188A	GRCh38.p7	10:15838287	CAAGGCAGCTATACA[C/T]AAAAGACACTTTTCA	80013
rs770226961	snp	C/T	5.15105e-05	0.0050747	utr-variant-5-prime, synonymous-codon, nc-transcript-variant	FAM188A	GRCh38.p7	10:15860267	CTTGGTGCCCCACAC[C/T]AGCTCCATCAGCTCT	80013
rs770266373	snp	C/T			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15783818	TAATTTGACTCTTGG[C/T]TATCAGAGTTAAATT	80013
rs770270511	in-del	-/AAAG			intron-variant	FAM188A	GRCh38.p7	10:15816605	AAAAGCTAAAGCTCT[-/AAAG]AAAGAAGAAGAAATT	80013
rs770274653	snp	A/G	1.67108e-05	0.00289052	intron-variant	FAM188A	GRCh38.p7	10:15834498	GAAGTCAAGTTTCTA[A/G]AAACTGGAGTTCACA	80013
rs770316705	snp	A/G	5.38459e-05	0.00518846	intron-variant	FAM188A	GRCh38.p7	10:15860176	GCAAAAGAAGCAGCG[A/G]CTGCAAGTGTGAGAG	80013
rs770341170	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15796275	CATTGGAGTCAGAAG[A/G]CTTTGAGTTACATTT	80013
rs770419147	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15853704	GGAAAAGTATATGTG[C/T]AATTTTTTTAACTGC	80013
rs770490963	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15813906	AAATATTTACAAGGA[A/G]CTGCTGGGGAAAAAT	80013
rs770497189	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15804480	TCTTTAAAGTTTTTC[C/T]CATTAAGCCTTTCAT	80013
rs770516512	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15826593	GGAGGAAAGTTCAAC[G/T]GGAATAGATAATGTA	80013
rs770554056	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15801686	AAGAGAACCGCAACA[G/T]CAAGAACAACATGGA	80013
rs770573249	snp	C/T	3.38232e-05	0.00411223	intron-variant	FAM188A	GRCh38.p7	10:15786681	AAAAACAGTGGATAC[C/T]AGAGGAAAAAAAAAA	80013
rs770580917	in-del	-/A			intron-variant	FAM188A	GRCh38.p7	10:15837380	ACATTCATAAAAGGG[-/A]AAAATTTTTAAATTT	80013
rs770598458	in-del	-/A			intron-variant	FAM188A	GRCh38.p7	10:15836771	CAGGAGGTAACAGAT[-/A]AAAGAAGGAAACAAA	80013
rs770599365	in-del	-/G			intron-variant	FAM188A	GRCh38.p7	10:15789959	ACACAAAGTCCTTGT[-/G]GGGTAGTTTGAAATG	80013
rs770623365	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15854523	GACCTGAGTTCCAAA[A/C]ACTTGAGAGCCACTG	80013
rs770784670	snp	A/G	1.66338e-05	0.00288386	synonymous-codon, nc-transcript-variant, intron-variant	FAM188A	GRCh38.p7	10:15821710	TACTGCTGCTTGTTC[A/G]TGTATACCAAGAAGT	80013
rs770787767	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15845893	AGTGGCGTGATCTCG[A/G]CTCACTGCAACCTCC	80013
rs770795587	snp	A/C	3.30044e-05	0.00406216	utr-variant-5-prime, missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15843221	TCATACCTGAACAAT[A/C]CCGCCAAGAAGACTT	80013
rs770798183	snp	C/G			missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15834583	TCAAGGGTTCACTTG[C/G]ATCTTCAATTTCGTT	80013
rs770811755	snp	G/T			upstream-variant-2KB	FAM188A	GRCh38.p7	10:15861221	AAGAGGGCTTGTATT[G/T]CCCGAGCTTTGAATT	80013
rs770854212	snp	A/G			downstream-variant-500B	FAM188A	GRCh38.p7	10:15778110	CAGGGTTATTGGGTA[A/G]AAACATTTAGAAGTA	80013
rs770854715	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15829311	GGCAGAGCCGTCTGA[A/G]TAGAACAGTGGTTCT	80013
rs770868854	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15813122	ATCCTGTTCCCTTCC[G/T]TCCCACCTCCCCCAA	80013
rs770876592	snp	A/G	8.52638e-05	0.00652876	intron-variant	FAM188A	GRCh38.p7	10:15816951	TAAAACAAATAAACA[A/G]ATTAAAAATTTATAC	80013
rs770911542	in-del	-/TA			intron-variant	FAM188A	GRCh38.p7	10:15781029	TGAATAATTAGTGAT[-/TA]TATAAAGTACCTCCT	80013
rs770948397	in-del	-/AAAG			intron-variant	FAM188A	GRCh38.p7	10:15847588	TAGGATCTCTGTGTT[-/AAAG]AAGTCAAGAAACTTC	80013
rs770962824	snp	A/G	1.66651e-05	0.00288657	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15779149	TACATGACCTGTTGA[A/G]CAAAATAAAGCCACC	80013
rs770970075	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15808683	ACAGTTCTGTCATGG[A/G]TATTCACGTGTTCAT	80013
rs771057971	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15820997	TCTACTTCTTTCTCC[A/C]AAATCATGACATCTT	80013
rs771115886	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15818499	GACCAGTAATTTCAC[C/T]CCTGGGTATATACAA	80013
rs771168510	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15852398	TGTAGTTCAGGGCAG[A/G]ACTTAGGATTAGAGG	80013
rs771219612	snp	C/T	0.000233073	0.0107927	intron-variant, missense	FAM188A	GRCh38.p7	10:15837546	AGAACACCTACTTGG[C/T]AGGGAACCTCTTCAT	80013
rs771229097	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15857897	ATATTCATGCCAAAC[A/T]TCTTACATCTGTATC	80013
rs771260990	in-del	-/AGTA	1.74494e-05	0.00295371	intron-variant	FAM188A	GRCh38.p7	10:15838195	GCAATGTGTCCACAG[-/AGTA]AGTATTTTAAATGTT	80013
rs771265507	snp	C/G	1.68459e-05	0.00290219	intron-variant	FAM188A	GRCh38.p7	10:15789324	GAATCCATTATCTAG[C/G]GGGGAAAAAATCAGA	80013
rs771295355	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15798066	ATACAGTTATTCTTT[C/T]TATTCGCCATCTGTT	80013
rs771303038	snp	A/C	1.65026e-05	0.00287246	intron-variant	FAM188A	GRCh38.p7	10:15796075	TGAAGACATAAAACA[A/C]AGAGATGATGTTAAA	80013
rs771333930	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15800226	GTAGATACTAGTCTA[C/T]TTTTTCTACTACCAT	80013
rs771336934	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15857341	GGCCTGACCAGGACA[A/C]CCCACCCAGAACTCT	80013
rs771402485	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15793721	CTCAAACCATCAAAA[C/G]GTTGTTCTCCAAAGA	80013
rs771405365	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15795343	TGGATTTTCAGAGAG[C/G]AAAAGAGCAGATCAC	80013
rs771437666	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15825263	CAAATATTTCCAAAT[C/T]TGAAAAAAATCGAAA	80013
rs771458392	snp	C/G	1.64933e-05	0.00287165	utr-variant-5-prime, missense, intron-variant, nc-transcript-variant	FAM188A	GRCh38.p7	10:15847864	AGGAGTCTATGTTAC[C/G]TGAACAGGTGCAATA	80013
rs771489297	snp	A/G	1.67164e-05	0.00289101	intron-variant, missense, utr-variant-5-prime, nc-transcript-variant	FAM188A	GRCh38.p7	10:15838276	TCTTCGACAGCCAAG[A/G]CAGCTATACATAAAA	80013
rs771509698	in-del	-/AG			intron-variant	FAM188A	GRCh38.p7	10:15843714	AAGATTAACACTATT[-/AG]AGTCATCACTTTATT	80013
rs771519215	snp	A/G	5.65915e-05	0.00531907	intron-variant	FAM188A	GRCh38.p7	10:15860166	CTCTCGCAGGGCAAA[A/G]GAAGCAGCGGCTGCA	80013
rs771529605	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15849317	GCTAAAGGGTAGTAC[A/G]GGGGTAGGATGGAGG	80013
rs771530354	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15837384	TTCATAAAAGGGAAA[A/C]TTTTTAAATTTTCTT	80013
rs771538966	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15824996	AAATTTACTTTTATG[C/T]CAAGTTGTAATACAG	80013
rs771561081	in-del	-/ATTAGGA			intron-variant	FAM188A	GRCh38.p7	10:15823027	TTTGTCCATTTTTCC[-/ATTAGGA]TATATTTTCTTATCA	80013
rs771564714	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15827721	ACAAAAGAAAATAAC[G/T]CCTCCTCCCCAAAAG	80013
rs771608390	in-del	-/C			intron-variant	FAM188A	GRCh38.p7	10:15857891	GTATAAATATTCATG[-/C]CAAACATCTTACATC	80013
rs771620111	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15836215	AATCCCTTACACTTT[C/T]ATACTTGCAGTGCCC	80013
rs771690736	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15825039	ATTCTCACATGTTAC[A/G]ATTTATAGAATTTAT	80013
rs771690899	in-del	-/T			intron-variant	FAM188A	GRCh38.p7	10:15852962	GTGTATTAGGTATTG[-/T]TAAGTAATCTAGAGA	80013
rs771741023	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15793630	TACTGGTAGTAGAGA[A/G]AAGGGGAAAGATTGC	80013
rs771775976	in-del	-/TATT			intron-variant	FAM188A	GRCh38.p7	10:15789529	GCAAATACTTAAAAA[-/TATT]TATTTTTTAACTTGA	80013
rs771783690	snp	C/T	1.67433e-05	0.00289333	missense, downstream-variant-500B, nc-transcript-variant	FAM188A	GRCh38.p7	10:15782199	CATTGTAGTGGTAGA[C/T]AGTAAAAGATTCTGG	80013
rs771823165	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15800638	GCCACTAGTGATGCC[G/T]GAAGTTCTCCCAAGA	80013
rs771836301	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15844444	GTTTTAATTTTATTA[C/T]AAGTGAAAAATCATA	80013
rs771847937	snp	C/T	1.65362e-05	0.00287538	synonymous-codon, intron-variant, nc-transcript-variant	FAM188A	GRCh38.p7	10:15816847	TACCTTGGCAAAAAA[C/T]ACGGTGAGGTGAGTC	80013
rs771851051	snp	C/G			intron-variant, downstream-variant-500B	FAM188A	GRCh38.p7	10:15782292	AATTTCTAATCAACT[C/G]AAAGTAAAATGCATG	80013
rs771900414	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15780991	ATGGATAATATTTGA[C/T]CTATCTTGCAGGGAT	80013
rs771920260	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15853549	AACATACTTACTGCT[G/T]CAGTCAAAATTACTA	80013
rs771937459	snp	C/G	1.65315e-05	0.00287498	utr-variant-5-prime, synonymous-codon, nc-transcript-variant	FAM188A	GRCh38.p7	10:15841568	TAAAATATCACACAA[C/G]GTATGACAAAGGAGT	80013
rs772076697	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15840404	TTATTCCTTGCAAAT[C/G]TTACTACTATTAGAA	80013
rs772089278	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15850022	GACAGAAGAATATAA[A/G]TCGTGAAGATTTCAT	80013
rs772103181	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15820120	GTGTCATTAATTATT[C/T]CTATTAAATATTGTG	80013
rs772104566	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15819819	ACTGCTAAAACACTA[C/T]AGCAATATGTAAACA	80013
rs772115363	snp	C/T	3.32265e-05	0.0040758	synonymous-codon, nc-transcript-variant, intron-variant	FAM188A	GRCh38.p7	10:15821698	TGTTAAAAATCCTAC[C/T]GCTGCTTGTTCATGT	80013
rs772138200	snp	A/G	1.66813e-05	0.00288797	missense, downstream-variant-500B, nc-transcript-variant	FAM188A	GRCh38.p7	10:15779042	GTAACTCAATGTATG[A/G]CCATTTGGTTTGCAG	80013
rs772191019	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15816087	CCTGGCCAACATGGC[G/T]AAACTGTCTCTACTA	80013
rs772196885	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15831313	TGGCAGTGGGAGGGA[A/G]AATGTGTACTATGTG	80013
rs772237508	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15809859	GAGACAGAGGGTTAG[C/T]AGGAAAAGATGACTC	80013
rs772259645	snp	C/T	1.66454e-05	0.00288486	intron-variant	FAM188A	GRCh38.p7	10:15816926	CCAACCTAGAACAAA[C/T]GTAGCAAAATAAAAC	80013
rs772271551	snp	C/G			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15784961	GGTGGGACTGTGACA[C/G]GTCTTCCTCTAAAGC	80013
rs772275209	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15817321	TATAGTTTATCAAAT[A/G]AGTAGATTTATGAAT	80013
rs772363234	snp	C/T	1.65916e-05	0.00288019	utr-variant-5-prime, missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15837292	ACAGCATCTTTTAAT[C/T]CTGGTAAACTTCTGA	80013
rs772389296	in-del	-/TTCTTA			intron-variant	FAM188A	GRCh38.p7	10:15824913	TGTATTATGCCTGTT[-/TTCTTA]AACAGAATATATACT	80013
rs772398337	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15797560	TCTGCTATTACAAAA[A/T]ATGCTGAATCAAATA	80013
rs772461060	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15804177	GATTGCAAAACAATA[C/T]AGCTTTTAAAATTAT	80013
rs772466782	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15830884	GTTTGTGGCCTGGTC[A/G]TTACACATCACGATT	80013
rs772502569	snp	A/G	1.67055e-05	0.00289006	synonymous-codon, nc-transcript-variant	FAM188A	GRCh38.p7	10:15789300	ATCTTCCAGAAGTGA[A/G]TCGGGTATGAATCCA	80013
rs772567718	in-del	-/AAG	1.65891e-05	0.00287998	intron-variant	FAM188A	GRCh38.p7	10:15796225	TATTATGACATTAAA[-/AAG]AAAACAGATACTAGG	80013
rs772590892	snp	C/T	1.75748e-05	0.00296431	intron-variant	FAM188A	GRCh38.p7	10:15789197	CAATATGTCTTAAAC[C/T]TAATCGAATCTTTTT	80013
rs772603484	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15823449	TATGAAGATCCGGCT[A/G]TCTACTAATAAGCCA	80013
rs772640062	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15793689	TCACATTTAGGTATG[G/T]GGCTCTGGAGAAGTG	80013
rs772641020	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15794259	CATACTAAGTGTTCT[C/G]AGAACGCATGATTTG	80013
rs772657825	snp	A/T	1.70828e-05	0.00292252	intron-variant	FAM188A	GRCh38.p7	10:15837360	GGTATCATGATGAGA[A/T]TAACTACATTCATAA	80013
rs772696890	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15812096	ACAGGTGCCCAGCAC[C/T]ACGCCTGGGTAATTT	80013
rs772731590	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15804289	ATCTAATAGCCTACA[A/G]TCATGAAACAGATAT	80013
rs772757461	snp	C/G/T	1.65157e-05	0.0028736	utr-variant-5-prime, synonymous-codon, missense, intron-variant, nc-transcript-variant	FAM188A	GRCh38.p7	10:15847921	TTCTAATGCAGATCC[C/G/T]TCTGATTCACTAAAC	80013
rs772763799	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15825045	ACATGTTACGATTTA[C/T]AGAATTTATTTGTAG	80013
rs772780270	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15836159	TTATGCTACAGTAAG[G/T]CTCAACTACTTAGAG	80013
rs772895682	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15832117	GGACTAGGGTAAGCT[A/G]TCGAGAATCCGGAGA	80013
rs772918739	in-del	-/TACT	2.0484e-05	0.00320025	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	FAM188A	GRCh38.p7	10:15778980	GATCTTCCTTATAAA[-/TACT]TAGACAAATTAATTT	80013
rs772922959	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15801476	TAAGAGACCACCTTT[C/T]AAAGTTCTTTTGATA	80013
rs772926846	snp	C/T	6.64496e-05	0.00576371	utr-variant-5-prime, missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15841456	GGCAACTAGACTCTG[C/T]AGGACTCCCAGAAAT	80013
rs772983195	in-del	-/TAA			upstream-variant-2KB	FAM188A	GRCh38.p7	10:15862037	CATTACAATTGAAAG[-/TAA]TAATTATAATTTCTG	80013
rs772992536	in-del	-/ATAT			utr-variant-3-prime, nc-transcript-variant	FAM188A	GRCh38.p7	10:15778582	TCATTGTAGAGGCTG[-/ATAT]ATTACAAGCCGGAAT	80013
rs772992864	snp	C/G	4.9606e-05	0.00498002	missense, intron-variant, nc-transcript-variant	FAM188A	GRCh38.p7	10:15786568	TATGTTACCTGATCA[C/G]GAAAAAATTCTTGAA	80013
rs773041134	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15800687	AGAAAAAGTGGAATT[C/G]CTTGATATGCACCAT	80013
rs773044336	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15858976	GTAGGGTTTGGGAAC[C/T]CAAAGGAAGATAATG	80013
rs773091677	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15815614	TTCAGCAACCTATCA[A/T]GTTACCTATGATCCC	80013
rs773102597	snp	A/T	0.000218864	0.0104587	intron-variant	FAM188A	GRCh38.p7	10:15816936	ACAAATGTAGCAAAA[A/T]AAAACAAATAAACAA	80013
rs773126235	snp	C/G	4.69054e-05	0.00484257	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	FAM188A	GRCh38.p7	10:15778945	CAGTCTTGACTCCTT[C/G]TTTCAACATCTGTTA	80013
rs773134899	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15859909	CGGGGCGCATCTTCC[C/G]TGTCACGCCCTGCAA	80013
rs773138619	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15841620	AATAACCAAAGCATA[A/C]GTTATAATGGTTTCC	80013
rs773190441	snp	C/T	1.65441e-05	0.00287607	utr-variant-5-prime, missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15841575	TCACACAAGGTATGA[C/T]AAAGGAGTTCCTTCT	80013
rs773192645	snp	C/T	4.96093e-05	0.00498018	missense, intron-variant, nc-transcript-variant	FAM188A	GRCh38.p7	10:15816849	CCTTGGCAAAAAATA[C/T]GGTGAGGTGAGTCTC	80013
rs773216658	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15788769	CGATATGCCATAATA[C/T]ATTGCAGCCATCCCT	80013
rs773246172	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15819887	CTTGAGGGGAAAAAC[A/G]TTCTTCTGTTCTACC	80013
rs773256082	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15828384	GTAAATCTATAGAGA[C/G]AAAGTAGATGAGCGG	80013
rs773323032	snp	C/T			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15784984	TCTAAAGCAGCTGTT[C/T]TCTAACTTGGGCCTC	80013
rs773350595	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15840425	ACTATTAGAATTTGC[C/T]AGGCTTAAGGCATTT	80013
rs773358023	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15842309	AGTTCTTTAACTGCA[A/G]GAACTATGCTGTTCA	80013
rs773371657	snp	A/C/T	8.62078e-05	0.0065649	utr-variant-5-prime, nc-transcript-variant	FAM188A	GRCh38.p7	10:15860313	ATGATGAGGAACCGG[A/C/T]GGGCGGATCTTCGCT	80013
rs773379297	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15829163	CCATAGATGATCAGA[C/G]GGAGGAGAAAACTTT	80013
rs773380405	in-del	-/CTTT			intron-variant	FAM188A	GRCh38.p7	10:15788086	TTGGAAAAAAAAAAA[-/CTTT]CTTCTTTCTCTTCCT	80013
rs773381447	in-del	-/G			intron-variant	FAM188A	GRCh38.p7	10:15798683	TACTTGGGAGGCTGA[-/G]GCAGGAAAATCATTT	80013
rs773426467	in-del	-/CC			intron-variant	FAM188A	GRCh38.p7	10:15802200	TGCAGGGGGTTAGCA[-/CC]CCAACTCCCATGTTA	80013
rs773445090	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15809935	AAATTTAAAAACTTA[A/C]AATTATATTTCTTCA	80013
rs773446092	snp	A/G			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15786439	AGGTTTCCATGTAAC[A/G]GTGTTTTCTCAGTCT	80013
rs773498304	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15856714	GAAGTTTGCCAAACA[C/T]TGAGCTAAGCAATCA	80013
rs773539322	in-del	-/TATC			intron-variant	FAM188A	GRCh38.p7	10:15793109	ATATTAATATATCTT[-/TATC]AATCATTTTACAATA	80013
rs773577593	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15817330	TCAAATGAGTAGATT[C/T]ATGAATAATCAAAGG	80013
rs773585371	in-del	-/A	0.000688729	0.0185443	intron-variant	FAM188A	GRCh38.p7	10:15816809	CTGATGTCATAACTT[-/A]AAAAAAAATCCTGCT	80013
rs773587123	snp	C/T	1.75705e-05	0.00296394	intron-variant	FAM188A	GRCh38.p7	10:15789201	ATGTCTTAAACTTAA[C/T]CGAATCTTTTTGAGT	80013
rs773648356	snp	C/T			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15784405	TTTTCCTGGCTGTCC[C/T]TGTCACTCCAGTTTT	80013
rs773766003	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15857783	AACAACTATGTGCCA[C/T]TCCTGCAGCTTATTG	80013
rs773800979	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15833832	ATTTACAAAGTTAGG[G/T]AAAACCTTACATTTT	80013
rs773823044	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15821008	CTCCCAAATCATGAC[A/G]TCTTACGAAGTGCAA	80013
rs773825219	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15853528	CAACTACAGAGCCAA[C/T]TTAAGAACATACTTA	80013
rs773832764	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15822302	TGACTTTACCAAAGA[C/T]GACAGATGAAAAAAA	80013
rs773837903	snp	A/C			intron-variant, synonymous-codon	FAM188A	GRCh38.p7	10:15780934	GTGTGACCCTGGGTG[A/C]GTCACTTGATCTCCC	80013
rs773915293	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15850448	TTGCTGAATTCTTTT[G/T]CTCAGCAAGGAACAG	80013
rs773933385	snp	A/C	3.41851e-05	0.00413417	intron-variant	FAM188A	GRCh38.p7	10:15821759	AACAACAAAAAACGA[A/C]AACTTAGCATTGTAG	80013
rs773948462	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15799442	GACCTCATGATCCAC[A/C]CACCTCAGGTTCCTA	80013
rs773957476	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15823382	TCTCATAAGCACAGA[C/G]TTTTACAGAGGTTGA	80013
rs773994140	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15792215	CAAGTCACACACCAG[A/C]GCTGAGCTTTTCCAG	80013
rs773997028	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15851819	TTCAGTGGCTTCTCA[C/T]TGCAATTAAAATAAA	80013
rs774020952	snp	A/T	1.65206e-05	0.00287403	intron-variant	FAM188A	GRCh38.p7	10:15843277	AAAAGAAATGCCTTT[A/T]CACAATTAAAGCAAT	80013
rs774071261	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15852661	ATACTAGATTAATCA[A/T]GTCATTGGGAATACT	80013
rs774073399	in-del	-/G			intron-variant	FAM188A	GRCh38.p7	10:15848366	TTGGCCGGGCACAGT[-/G]GCTCACGCCTGTAAT	80013
rs774121866	in-del	-/AA			intron-variant	FAM188A	GRCh38.p7	10:15804594	TATAAATGACATTTT[-/AA]AGCTTGCAGACAACA	80013
rs774130641	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15812902	CAATCCAATCCATCA[C/G]CCAGTCCTGTCATTC	80013
rs774134190	snp	A/G	1.67066e-05	0.00289016	utr-variant-5-prime, synonymous-codon, nc-transcript-variant	FAM188A	GRCh38.p7	10:15841442	AGAATGTTCCACTTG[A/G]CAACTAGACTCTGCA	80013
rs774204974	snp	A/C	1.65056e-05	0.00287272	missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15833662	CTATCACCATCCCAT[A/C]CATTAGAAACAGCAT	80013
rs774240028	snp	C/T	1.6795e-05	0.0028978	synonymous-codon, downstream-variant-500B, nc-transcript-variant	FAM188A	GRCh38.p7	10:15782173	TTCATTATAATTTGA[C/T]TGCTTCAATCCATTG	80013
rs774291681	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15808403	GCACCACTTTACAGC[A/T]TTTCCTTAACACCGT	80013
rs774325703	snp	C/T	4.94694e-05	0.00497316	synonymous-codon, nc-transcript-variant	FAM188A	GRCh38.p7	10:15796137	AACTCTTCTGGCTTG[C/T]TCTGAAGGAGCTTCA	80013
rs774354487	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15842029	GTCTATGATCACCCC[A/G]TCCCAAAGGGATAAG	80013
rs774366534	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15800606	CTTGAAAAAAAACCA[C/T]GGAACCCATATGAAG	80013
rs774380407	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15850667	CTCCTGATAAGATGT[A/T]ATCAATGACAATGCC	80013
rs774384454	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15838480	TAACTAAAATCGATA[C/T]AATACTGAGAATATA	80013
rs774417425	snp	C/T	1.69281e-05	0.00290925	intron-variant	FAM188A	GRCh38.p7	10:15838316	CAGCACTACACATGG[C/T]AAATAAATGACACAA	80013
rs774459150	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15796363	CTGAAAAGTGGCAAT[A/G]AAAGCTTAACCACAG	80013
rs774469837	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15849693	GACACCAGGTGAGAG[C/T]AATGGAGAGGGTGCC	80013
rs774510570	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15840313	ATAAACTCTAAAATA[C/T]GTTAAGTTCTTTTTG	80013
rs774527932	in-del	-/AC			intron-variant	FAM188A	GRCh38.p7	10:15824674	TACATACATTGGGAA[-/AC]AGTTTCACAATTTAA	80013
rs774587812	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15820869	CCAGCACTTAGGGAT[A/G]GAAGCCAAGGTAGGA	80013
rs774634927	snp	A/T	0.000864543	0.0207732	intron-variant	FAM188A	GRCh38.p7	10:15834640	ACAGAATTCATTGAC[A/T]TATTTTAAAAAACTA	80013
rs774664610	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15846932	GTTTCACCATGTTAG[A/C]CAGGATGGCCTCCAT	80013
rs774686334	snp	C/T			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15784760	AAATAGTTTACGGAA[C/T]GATCACTATATTCAT	80013
rs774739384	snp	C/T			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15784054	TTAAGTTCTCTAATC[C/T]TCAATTTCCTCATTG	80013
rs774762904	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15817254	TTTCAGCATGAAACC[C/T]CAAACCCTAAAACTA	80013
rs774786969	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15828156	GTACCTCACAGCATT[A/G]CTCATAATGGCCAAG	80013
rs774875457	in-del	-/A	0.00157698	0.0280357	intron-variant	FAM188A	GRCh38.p7	10:15841640	AATGGTTTCCTCTGG[-/A]AAAAAAAAAAATTCT	80013
rs774879648	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15801829	AGTTCATAGGATTTA[C/T]AGAGCCAATCAGAGT	80013
rs774882009	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15793584	AAAGGTTAAAAAGTA[C/T]CTTTTTATGACTTTA	80013
rs774899055	snp	C/T	3.31011e-05	0.0040681	missense, intron-variant, nc-transcript-variant	FAM188A	GRCh38.p7	10:15786613	AATATGATTCCTAAT[C/T]CTTCTGGATCTAATT	80013
rs774900741	snp	C/T	1.65679e-05	0.00287814	utr-variant-5-prime, missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15837283	TGGTCCAAGACAGCA[C/T]CTTTTAATTCTGGTA	80013
rs774904493	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15854885	GTTAAAACAACCAAA[A/T]TTAAGGTCCAACCTA	80013
rs774958218	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15832798	GTTTCTGTTAATTAA[C/T]TACACATTTCTGAAT	80013
rs774967835	in-del	-/T			intron-variant	FAM188A	GRCh38.p7	10:15788633	ACTTAAGAAGAGTTA[-/T]TTTTTTCATGGATAA	80013
rs774975329	in-del	-/A			intron-variant	FAM188A	GRCh38.p7	10:15846308	TCATGCACTTGCAAC[-/A]AAAACCTTGCTATTA	80013
rs774983172	in-del	-/TGT	1.65002e-05	0.00287225	intron-variant	FAM188A	GRCh38.p7	10:15796084	AAAACACAGAGATGA[-/TGT]TAAAATCTTTTACCT	80013
rs774985868	snp	A/C	6.7807e-05	0.00582227	intron-variant	FAM188A	GRCh38.p7	10:15821752	CAACAACAACAACAA[A/C]AAACGAAAACTTAGC	80013
rs775029217	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15856170	GGTGTGTCATTTTAT[A/T]ACTTTGATAAAATAG	80013
rs775046210	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15846021	AGAGACGAGGTTTCA[C/T]CACATTGGCCAGGCT	80013
rs775071877	snp	A/G	1.66704e-05	0.00288703	intron-variant	FAM188A	GRCh38.p7	10:15841614	TCTAAAAATAACCAA[A/G]GCATAAGTTATAATG	80013
rs775080504	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15857892	TATAAATATTCATGC[C/G]AAACATCTTACATCT	80013
rs775082707	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15833776	AATAATTCCTACAGC[A/G]AAGTATAAAGTAATG	80013
rs775112191	snp	G/T	1.66029e-05	0.00288117	missense, downstream-variant-500B, nc-transcript-variant	FAM188A	GRCh38.p7	10:15779071	AGACAGCGTTTAATA[G/T]GAGTGTCATCTGTCT	80013
rs775134750	snp	A/G			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15779451	GGATCTATACCATCG[A/G]AAAGAAATGCTTAAT	80013
rs775139361	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15802554	TCCCTCCTTACTATG[C/T]GAGATGAGATCTGGG	80013
rs775140840	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15810253	AATTATATTTAATTA[A/C]TTTAAGTCCTAAAAG	80013
rs775155960	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15815972	AATTTTGAAATAGAA[A/T]TATTCAGATATGGCG	80013
rs775168882	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15855131	GCGTTACAGTGAGTT[A/G]CTTTTGTACTTTTAA	80013
rs775300097	snp	A/C			utr-variant-3-prime, nc-transcript-variant	FAM188A	GRCh38.p7	10:15778291	AAATATAGAAGAAAG[A/C]TGGCTTACAGGGCTG	80013
rs775319044	snp	C/T	1.65482e-05	0.00287643	intron-variant	FAM188A	GRCh38.p7	10:15833625	ATAACAAGGAATATA[C/T]TTACTCATTCCTGAG	80013
rs775350736	snp	G/T	1.64999e-05	0.00287222	utr-variant-5-prime, missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15843238	CGCCAAGAAGACTTC[G/T]CCGAAGAAAACAGGA	80013
rs775389112	snp	C/T	1.68057e-05	0.00289872	intron-variant, utr-variant-5-prime	FAM188A	GRCh38.p7	10:15838294	GCTATACATAAAAGA[C/T]ACTTTTCAGCACTAC	80013
rs775395741	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15851651	CCTATAGTTCAAACC[A/G]CTATAATCTTTGACC	80013
rs775447684	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15841918	TAGCAACTGCAGCAT[G/T]TAAGCCAAGAGGTTT	80013
rs775472396	snp	G/T	5.25334e-05	0.00512484	intron-variant	FAM188A	GRCh38.p7	10:15838186	CTTAAAGTGGCAATG[G/T]GTCCACAGAGTAAGT	80013
rs775483564	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15839039	CAGCAGAGATGAGAC[C/T]TGAGCACAGATAGTC	80013
rs775484080	snp	A/G			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15782672	TCCAATTTGGCCCAC[A/G]ATGTTTAATTAGTGG	80013
rs775513306	snp	C/G	8.375e-05	0.00647055	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15779173	AGCCACCAAGGTCAA[C/G]CAACAGTCTTAGCAA	80013
rs775515501	in-del	AAAAGCC/TAGAAGCCATCTA			intron-variant	FAM188A	GRCh38.p7	10:15827206	AAAAAAAAGCCCAAA[AAAAGCC/TAGAAGCCATCTA]AAAAAAAGACCAAAT	80013
rs775518505	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15859847	CTCTGTTAGGGGGTA[A/C]AGATGCGGAAGGCCA	80013
rs775525843	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15836496	ATAGAGTCAATCAAC[A/G]CTCAAAAAACATTTG	80013
rs775534360	in-del	-/AA			intron-variant	FAM188A	GRCh38.p7	10:15805104	TGTGCCATAATTATT[-/AA]AATCATTAATGAGTG	80013
rs775540775	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15842028	CGTCTATGATCACCC[C/T]GTCCCAAAGGGATAA	80013
rs775548714	in-del	-/AAAGAA			intron-variant	FAM188A	GRCh38.p7	10:15797649	TGGGATGGCTGGGTC[-/AAAGAA]AGGTTTATTTAACCT	80013
rs775595602	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15798039	GGGAACTTACAGGGG[A/C]ACAAAATCAGGATAC	80013
rs775617678	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15807279	ACAGTAGGTAGTGTG[C/G]GAAATCAGTTAGTGC	80013
rs775622419	in-del	-/A			intron-variant	FAM188A	GRCh38.p7	10:15838497	ATACTGAGAATATAG[-/A]AGGGTGATTAAATAA	80013
rs775641246	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15849433	TCAGTAAAACAGTAA[C/T]ATCATCTTACTGGTT	80013
rs775716519	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15831288	GTTTCTTTTCTAGCA[A/C]TAATCAGCCTGGCAG	80013
rs775764037	snp	A/C	5.17103e-05	0.00508453	intron-variant	FAM188A	GRCh38.p7	10:15860181	AGAAGCAGCGGCTGC[A/C]AGTGTGAGAGCCCCG	80013
rs775782369	in-del	-/AAT			intron-variant	FAM188A	GRCh38.p7	10:15804749	ACAAATAATTTGGGA[-/AAT]AATAGATTTTAAGTC	80013
rs775805643	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15854686	AAAAACATAAGGAAA[A/G]AACTAAGAGAAGCAC	80013
rs775822193	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15827977	ACTTTTACCAGTTGA[C/T]AAAGCAAATTTTAGA	80013
rs775825458	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15796343	CCAGGCCATTTATTT[C/T]ACGTCTGAAAAGTGG	80013
rs775826391	snp	A/G	3.4659e-05	0.00416273	intron-variant, downstream-variant-500B	FAM188A	GRCh38.p7	10:15782229	GACCACTGGAGCCCT[A/G]TTATAAATAAAGGAC	80013
rs775828732	snp	A/G	1.68083e-05	0.00289894	intron-variant	FAM188A	GRCh38.p7	10:15816796	AATACTTGTTTGCCT[A/G]ATGTCATAACTTAAA	80013
rs775916637	snp	A/C	1.64885e-05	0.00287123	missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15796126	TAGGTTTGAAAAACT[A/C]TTCTGGCTTGTTCTG	80013
rs775938855	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15800725	GGTCTGCTGCTGTGG[G/T]TGCTCACTATGTCAA	80013
rs775941994	snp	C/T	3.43843e-05	0.0041462	intron-variant	FAM188A	GRCh38.p7	10:15834635	AAGAAACAGAATTCA[C/T]TGACTTATTTTAAAA	80013
rs775990629	snp	C/T			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15783949	AGTGTAGCCCACTGG[C/T]AAAGTGCATAGACTC	80013
rs775990652	in-del	-/A			intron-variant	FAM188A	GRCh38.p7	10:15818318	AATTAAGGTAGAAGT[-/A]AAAAAAAAAAACAAA	80013
rs776029935	snp	A/T	0.000116892	0.00764409	intron-variant	FAM188A	GRCh38.p7	10:15834500	AGTCAAGTTTCTAAA[A/T]ACTGGAGTTCACATG	80013
rs776033737	snp	A/G	5.22207e-05	0.00510956	utr-variant-5-prime, synonymous-codon, nc-transcript-variant	FAM188A	GRCh38.p7	10:15860278	ACACCAGCTCCATCA[A/G]CTCTTTAGTCAGTTC	80013
rs776084672	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15844778	AGTATATGAGTGTGC[C/T]AGCATCTTCCCACCC	80013
rs776090962	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15854574	TTTAGAAGGCTTTTA[A/G]GTTAAACATATGAGG	80013
rs776137901	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15799636	AATTCTAGCTAGAAG[C/G]AACGGAATCAGGAAA	80013
rs776185845	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15853766	GGAGTGCTGCTTTTA[C/G]CTAGTATAACTACCA	80013
rs776231187	in-del	-/AAAT	1.69137e-05	0.00290802	intron-variant	FAM188A	GRCh38.p7	10:15816942	GTAGCAAAATAAAAC[-/AAAT]AAACAAATTAAAAAT	80013
rs776276336	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15821034	TGCAAGTCAATAATG[C/G]TTTAAATTCCATTTA	80013
rs776290826	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15832674	AATTAAATAAGAAGT[A/G]AACTTAGTTCTTAAA	80013
rs776293512	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15826662	GAAACATGCTAATGA[A/G]TATCAAAGTATATTA	80013
rs776299021	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15858319	TTAAAGAATTTCTGC[A/G]TGATTAAAGGTGGCA	80013
rs776317466	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15802467	ATCAAACAACCAGAT[C/G]TCCTGAGAACTCACT	80013
rs776321071	in-del	-/C	1.69464e-05	0.00291083	intron-variant	FAM188A	GRCh38.p7	10:15838323	CACATGGCAAATAAA[-/C]TGACACAAGATACAC	80013
rs776335734	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15860091	TTCAGCGCTGAGCAC[C/G]GCGACTGGGGCAGAG	80013
rs776366672	snp	A/T	5.17728e-05	0.0050876	intron-variant	FAM188A	GRCh38.p7	10:15816958	AATAAACAAATTAAA[A/T]ATTTATACTGCCTCT	80013
rs776391548	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15801766	GCTAATCCATCTGGC[C/T]CAAAACATATTCCTG	80013
rs776394608	in-del	-/AAA			intron-variant	FAM188A	GRCh38.p7	10:15827177	TGATATAACAGGAGT[-/AAA]AAAAAAAAAAAAAAA	80013
rs776405468	snp	A/C			upstream-variant-2KB	FAM188A	GRCh38.p7	10:15860936	TACTTCAATAAATCA[A/C]AGTCAGACCAACTAT	80013
rs776410247	in-del	-/A			intron-variant	FAM188A	GRCh38.p7	10:15812473	CCCATGCAATATTAG[-/A]AAAGTTTTTAATTCC	80013
rs776542217	snp	A/G	1.66087e-05	0.00288168	synonymous-codon, downstream-variant-500B, nc-transcript-variant	FAM188A	GRCh38.p7	10:15779067	TTGCAGACAGCGTTT[A/G]ATAGGAGTGTCATCT	80013
rs776556593	snp	C/G			downstream-variant-500B	FAM188A	GRCh38.p7	10:15778148	GTTTATTTTGAGCCA[C/G]CAATGTAAAAAATGC	80013
rs776556595	snp	G/T	4.53937e-05	0.0047639	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	FAM188A	GRCh38.p7	10:15778962	TTCAACATCTGTTAT[G/T]AAGATCTTCCTTATA	80013
rs776558569	snp	A/G	1.66977e-05	0.00288939	intron-variant	FAM188A	GRCh38.p7	10:15821729	ATACCAAGAAGTTCT[A/G]CAAAAAACAACAACA	80013
rs776559007	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15830137	ACATTATGGCAAGCT[G/T]CATAACCAATGTCTG	80013
rs776655366	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15848076	ATCATGAGGTGTGGA[A/T]CAAGGAACCTTTTGA	80013
rs776675239	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15817517	TACTCTGCTCTCAAG[A/G]TTACATAATCTGTGA	80013
rs776737502	snp	A/G			upstream-variant-2KB	FAM188A	GRCh38.p7	10:15861243	CTTTGAATTTAAAAC[A/G]AAAGGGCAAAATCTG	80013
rs776747639	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15808693	CATGGATATTCACGT[A/G]TTCATGCCTGACAAG	80013
rs776753384	snp	A/G			intron-variant, utr-variant-5-prime	FAM188A	GRCh38.p7	10:15857959	GTCAACTGAAGACAC[A/G]ATCACAGACTATGAA	80013
rs776776810	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15829331	ACAGTGGTTCTTAAC[C/T]CTGACTACACAATAT	80013
rs776784319	snp	A/G	1.67044e-05	0.00288997	utr-variant-5-prime, missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15837310	GGTAAACTTCTGAAC[A/G]ATCTTTTTCTGGGGG	80013
rs776808497	snp	A/C	4.94964e-05	0.00497451	intron-variant	FAM188A	GRCh38.p7	10:15796090	CAGAGATGATGTTAA[A/C]ATCTTTTACCTTCTG	80013
rs776875965	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15818549	CACAAAAAATTTGTA[C/T]ATCAATGTTTACAGC	80013
rs776879656	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15789328	CCATTATCTAGGGGG[G/T]AAAAAATCAGAAACA	80013
rs776895550	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15799255	CCCAGGCTGGAGTGC[A/G]GTGGTGTGATCTTGC	80013
rs776980013	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15807140	GAGGAATGCTCCTGA[G/T]ATGATTAATTAGCAT	80013
rs776980502	snp	C/T	1.65127e-05	0.00287334	synonymous-codon, nc-transcript-variant	FAM188A	GRCh38.p7	10:15833679	ATTAGAAACAGCATG[C/T]CCCGTCAGCAGGAGA	80013
rs777001821	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15787665	CATCTCTCCCGGAAA[C/T]ACCTGGGTCAGGCTG	80013
rs777053400	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15793938	CACTATGGAAGATGT[C/G]GTCTCATAGAGGCAA	80013
rs777068683	snp	A/T	1.64931e-05	0.00287163	utr-variant-5-prime, synonymous-codon, intron-variant, nc-transcript-variant	FAM188A	GRCh38.p7	10:15847867	AGTCTATGTTACCTG[A/T]ACAGGTGCAATAACA	80013
rs777085035	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15807850	ATACAAATACAGCTG[C/T]ATAAGGCAAAGAGTA	80013
rs777103354	snp	C/G	2.54217e-05	0.00356514	utr-variant-5-prime, missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15860244	GTGTCCGAGAGACCG[C/G]GGCTGCTCTTGGTGC	80013
rs777169815	snp	A/C	0.000168128	0.00916711	intron-variant	FAM188A	GRCh38.p7	10:15860168	CTCGCAGGGCAAAAG[A/C]AGCAGCGGCTGCAAG	80013
rs777200029	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15835358	TTTAGCCATTGTTTC[C/T]ATCATATTAGAGGTC	80013
rs777212403	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15781178	GGATGCTGTATATAT[A/C]TATCTTTGGACCTGA	80013
rs777236595	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15837401	TTTTAAATTTTCTTA[C/T]ACATTAAAACATATA	80013
rs777236906	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15825275	AATCTGAAAAAAATC[A/G]AAATCTTAAATGCTT	80013
rs777258804	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15836884	TCAAGAAATGGAATC[A/C]AGGTCAAAAACAGCT	80013
rs777299410	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15795945	GCTATTTCATTTGTT[A/C]CCATTTTCACTACTT	80013
rs777326892	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15794975	ATCCTTTCCTTTTAT[A/G]TTTCTTTTCTCAAGA	80013
rs777371592	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15806993	CTCAGAAGTCAGAAG[A/G]CTGGAGTTTAAATCC	80013
rs777375342	snp	C/T			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15786438	AAGGTTTCCATGTAA[C/T]GGTGTTTTCTCAGTC	80013
rs777404704	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15836937	AGTGCTACACGGAAG[G/T]ATCAAAGGAAACACA	80013
rs777424898	in-del	-/G	1.68326e-05	0.00290104	intron-variant	FAM188A	GRCh38.p7	10:15789322	TGAATCCATTATCTA[-/G]GGGGGGAAAAAATCA	80013
rs777441425	in-del	-/T			intron-variant	FAM188A	GRCh38.p7	10:15796339	TCTCCAGGCCATTTA[-/T]TTTTACGTCTGAAAA	80013
rs777452065	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15813639	ATAATGCCAGGCACA[A/T]ACTATAATCCAGTAA	80013
rs777520834	snp	C/T			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15783727	TGTTTTGTATCCCAC[C/T]CAAAATGCCTTACAG	80013
rs777527855	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15846513	GGCAAGATTCAGACA[C/T]TCAAATTTTTCCTCA	80013
rs777556990	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15815122	CATTTTTGTGTGTAA[A/G]TCAGAATTAATTTTC	80013
rs777561427	in-del	-/A			intron-variant	FAM188A	GRCh38.p7	10:15813979	AACTCACCAAAACTC[-/A]AAAAAAAAAAAAAAA	80013
rs777580318	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15821916	AATACCATTAGATCA[A/G]GTTTGTGGTGGGTAA	80013
rs777606461	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15839066	AGTCTTGGCTCCAGG[C/G]AGTTATTTATCACAA	80013
rs777642672	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15827654	AATATTTGCAACACA[G/T]GTCAAACAGAGGAAG	80013
rs777650296	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15790059	CATTCCTGAAGATTG[G/T]CTCAGCTTTAAATCA	80013
rs777654053	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15803269	ACACTAATTTTTGCC[A/G]ATTTATTTAACTTAA	80013
rs777685974	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15854371	ACAGACTGGAGAAGC[C/T]AGTGTAGGAATCCAG	80013
rs777734347	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15822802	AAGTTATGGAAGTGG[C/G]TAAGTCAGAACAGAC	80013
rs777743965	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15802382	ATCATGCCAGACAGC[A/G]AAGGAGAAGCAAGCA	80013
rs777757716	snp	A/T	1.68343e-05	0.00290118	intron-variant	FAM188A	GRCh38.p7	10:15786678	AAGAAAAACAGTGGA[A/T]ACCAGAGGAAAAAAA	80013
rs777780928	snp	C/G	1.66197e-05	0.00288263	missense, nc-transcript-variant, intron-variant	FAM188A	GRCh38.p7	10:15821702	AAAAATCCTACTGCT[C/G]CTTGTTCATGTATAC	80013
rs777781030	snp	A/G	1.65839e-05	0.00287953	intron-variant	FAM188A	GRCh38.p7	10:15843323	TTATAACCATACATC[A/G]TATCATTCTTCAATT	80013
rs777880686	snp	C/T	1.69617e-05	0.00291214	intron-variant	FAM188A	GRCh38.p7	10:15789237	AAATAACACTTCCTA[C/T]TTAGCTTACTATTCA	80013
rs777889245	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15852376	TTAGAAATCGGAGAT[A/G]TAAGTGTGTAGTTCA	80013
rs777965777	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15858715	CTTCCTTGTATTTGC[A/G]TTACAGTATAAATAT	80013
rs777971741	snp	C/G	1.6659e-05	0.00288604	intron-variant	FAM188A	GRCh38.p7	10:15833583	CAGCTGTATTCCAAT[C/G]AAATATTATTCATCA	80013
rs778138092	snp	G/T	2.04146e-05	0.00319482	intron-variant	FAM188A	GRCh38.p7	10:15841402	AACAAGAAAAAAACT[G/T]CAGGAAATAAAAATA	80013
rs778157684	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15798822	CTATGCCAACGTAGA[A/C]AGAAATTAAAGTAAA	80013
rs778194528	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15812663	TACAAGAAGAAAGTC[A/G]TGTCAGAGAAGCTAC	80013
rs778206308	in-del	-/ATA			intron-variant	FAM188A	GRCh38.p7	10:15859724	ACCACGCCTAACCAC[-/ATA]ATGACAATACAAACA	80013
rs778209018	in-del	-/A	0.000118139	0.00768478	intron-variant	FAM188A	GRCh38.p7	10:15837325	ATCTTTTTCTGGGGG[-/A]AAAAAAAGAATTAAG	80013
rs778217418	snp	G/T	0.000185006	0.00961607	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15779183	GTCAAGCAACAGTCT[G/T]AGCAAATTCTTATGT	80013
rs778217760	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15819208	TTATCAAAGCACGGG[A/G]AAATGTTCAGACTTA	80013
rs778245603	in-del	-/TTC			intron-variant	FAM188A	GRCh38.p7	10:15843489	TCTAGATTCATAAAA[-/TTC]TTCTTCTTCCACAAT	80013
rs778266988	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15848511	TGGTGGTGGGCAACT[G/T]TAGTCCCAGCTACTC	80013
rs778298784	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15819340	GATGAACACTGTAGC[A/G]TAATATAGTTTTTCA	80013
rs778338898	snp	C/T	1.6507e-05	0.00287284	intron-variant	FAM188A	GRCh38.p7	10:15796060	TGTATTTCAAACATA[C/T]GAAGACATAAAACAC	80013
rs778355325	snp	G/T	1.67055e-05	0.00289006	intron-variant, missense, utr-variant-5-prime, nc-transcript-variant	FAM188A	GRCh38.p7	10:15838270	CCAAGCTCTTCGACA[G/T]CCAAGGCAGCTATAC	80013
rs778371925	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15848561	ATGGCGTGAACCTAG[C/T]AGGCGGAGCTTGCAC	80013
rs778451190	in-del	-/A			utr-variant-3-prime, nc-transcript-variant	FAM188A	GRCh38.p7	10:15778244	ATATACTAATGTAAT[-/A]ACAGATCTTCTCATG	80013
rs778512752	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15811076	TCAGTTTTCAAACTC[C/T]GCCAATTATTTTGAT	80013
rs778584261	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15849230	GAATTCAGCTAAAGA[A/C]AATACCTTAATTAAA	80013
rs778594342	snp	A/G	2.60088e-05	0.00360607	utr-variant-5-prime, missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15860238	AAAATGGTGTCCGAG[A/G]GACCGGGGCTGCTCT	80013
rs778665410	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15854184	TTTGGTTTTAGATTT[C/T]GTATTGCAACTAATC	80013
rs778670516	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15794783	GCAAACAAAGCTACT[A/G]CTTATGACAACTGTC	80013
rs778678807	snp	A/G	1.93673e-05	0.00311179	intron-variant	FAM188A	GRCh38.p7	10:15833748	ATTAAATATGAATAT[A/G]GTTGCCAAATCAAAT	80013
rs778682632	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15843909	TATCCCAGTCACCTG[A/T]CTTGTTTAAATTGCA	80013
rs778693679	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15824863	CAGTAAACACATGCT[C/T]AGACATCTAGTCTGG	80013
rs778716048	snp	A/C					GRCh38.p7	10:15789874	CTGAAATGAAGAGTC[A/C]AACTAATGCTGATGA	80013
rs778721763	snp	G/T					GRCh38.p7	10:15793546	TCCATTAAATTAACA[G/T]TTCAAAGTAAACTTA	80013
rs778735658	snp	A/T					GRCh38.p7	10:15853435	TAATACATTGCTGGT[A/T]CCTTAGCATACATCG	80013
rs778759237	in-del	-/CTTT					GRCh38.p7	10:15820475	CGCCTCCATGCTTAA[-/CTTT]CTTTAGGATCTACGA	80013
rs778786488	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15836915	TCCAGAAGGGGTTAA[C/G]GGGTCAAGTGCTACA	80013
rs778801241	snp	C/T	4.96997e-05	0.00498472	missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15834595	TTGCATCTTCAATTT[C/T]GTTTTTTATGTTTTC	80013
rs778806157	in-del	-/GAA			intron-variant	FAM188A	GRCh38.p7	10:15787323	GTGACTAGAAAGAAG[-/GAA]GAAGAAGGCAGAAGA	80013
rs778904496	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15829461	CTAGTTAATCGTGAT[A/G]TGCAGCCAAGTTTGA	80013
rs778914713	snp	A/G			upstream-variant-2KB	FAM188A	GRCh38.p7	10:15861156	TTTTACTCATTAACT[A/G]GCAGTTAAATTGAGT	80013
rs778924662	snp	C/T	1.65239e-05	0.00287431	utr-variant-5-prime, missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15841549	GGTCACAACAAGCAC[C/T]TTCTAAAATATCACA	80013
rs778944765	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15791526	ATCAACACAAAAGAA[C/T]GGGGACTATGAGGCA	80013
rs778946559	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15844001	TTACAATGACGACTT[C/T]TCCTCACCTGTGTTT	80013
rs778957969	in-del	-/AAAT			intron-variant	FAM188A	GRCh38.p7	10:15815487	ACTTTCTACAGAAAC[-/AAAT]AATAAACTTTCATTG	80013
rs778975828	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15847780	GTCTCATAATTACTA[C/T]ATGGAGTACAGACAT	80013
rs778979220	snp	A/G	1.66421e-05	0.00288458	intron-variant	FAM188A	GRCh38.p7	10:15786655	AGATTTATACTACGG[A/G]GAGAAAGAAGAAAAA	80013
rs778986152	in-del	-/TG			intron-variant	FAM188A	GRCh38.p7	10:15841761	GTCTTAGAAAAACAA[-/TG]TGTTTGTGGATTAAA	80013
rs778997753	snp	C/T	1.65455e-05	0.00287619	missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15837258	AAATTTATTTCCCCA[C/T]ATTGAATACTGGTCC	80013
rs778997815	snp	A/G	3.31131e-05	0.00406884	intron-variant	FAM188A	GRCh38.p7	10:15786551	GAATATATTTCCTCA[A/G]CTATGTTACCTGATC	80013
rs779000415	snp	C/T	3.32143e-05	0.00407505	synonymous-codon, nc-transcript-variant, intron-variant	FAM188A	GRCh38.p7	10:15821680	TCTTAAAGCTTCCAT[C/T]AGTGTTAAAAATCCT	80013
rs779042012	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15834154	TTTTGGTAAAAATAG[A/C]CATAAAAAGCTTGAG	80013
rs779055131	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15851286	AGTCCATTCCTTGTT[A/G]TAACCATGTAATTCC	80013
rs779122981	snp	C/T	1.65285e-05	0.00287471	intron-variant	FAM188A	GRCh38.p7	10:15843191	GGAGGAAGCAAAAGT[C/T]TTAAAAGACAGCTAT	80013
rs779129875	snp	A/G	0.00012406	0.00787492	intron-variant	FAM188A	GRCh38.p7	10:15821774	AAACTTAGCATTGTA[A/G]TAGTGTGTATAAATT	80013
rs779134242	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15829113	AAGAACTATGATGCG[A/G]GGTGTAATAGAATGA	80013
rs779185199	snp	A/G	1.67089e-05	0.00289035	missense, downstream-variant-500B, nc-transcript-variant	FAM188A	GRCh38.p7	10:15779035	GTCCAGAGTAACTCA[A/G]TGTATGGCCATTTGG	80013
rs779208802	snp	A/C	4.98857e-05	0.00499403	intron-variant	FAM188A	GRCh38.p7	10:15816922	AGAACCAACCTAGAA[A/C]AAATGTAGCAAAATA	80013
rs779239750	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15842330	ATGCTGTTCACTTTC[G/T]AATCACCACAGTATT	80013
rs779249991	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15852207	GTTGTATCTGTGTTA[C/T]TGGTCATTGTTTTCC	80013
rs779267653	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15833062	AGTTATGTATCAGCT[A/C]TCCTTAACGGAATGG	80013
rs779326604	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15822739	AGGAGAGAAACGTCA[C/G]GGTTGGAGATAAAGA	80013
rs779337158	in-del	-/A			intron-variant	FAM188A	GRCh38.p7	10:15834453	ACACTACTGACAAAC[-/A]AAATTACTTGACTCA	80013
rs779357501	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15798397	CTGGCATTAAGGAGC[C/T]GACAGTTCAGGAGTG	80013
rs779362503	snp	C/T	1.7013e-05	0.00291654	intron-variant	FAM188A	GRCh38.p7	10:15837352	TAAGTATTGGTATCA[C/T]GATGAGATTAACTAC	80013
rs779399603	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15857361	CCCAGAACTCTGTAT[C/T]TCCTCATCTTCAAAC	80013
rs779417044	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15824592	GATACTTCATATCTT[C/T]GCAAACTTTTCTCTC	80013
rs779430558	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15787394	GTCTTCAGAAAAGTT[G/T]TATTTTCCTTGCTAT	80013
rs779450191	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15810881	CAATTAAAAAACAGG[C/T]GAAGGACCTGAACAG	80013
rs779481605	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15799957	TTGCAAGGGAAAATA[C/T]TGAAAACTTATGGAA	80013
rs779492480	snp	A/G	1.67091e-05	0.00289038	intron-variant, stop-gained, utr-variant-5-prime, nc-transcript-variant	FAM188A	GRCh38.p7	10:15838247	TTAATGCATGAAATC[A/G]CTCAAAGCCAAGCTC	80013
rs779492710	snp	A/G	1.6686e-05	0.00288838	missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15789274	GAAACAAGGTCCAAT[A/G]CTTTCATCACATCTT	80013
rs779503450	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15857575	GGCAATTGAGCAGGA[C/G]GAAAGCAGAGAGAAG	80013
rs779516492	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15829718	ACAGACAGAAAGCTA[C/T]AGCATGATAGTCTAG	80013
rs779519120	snp	C/G			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15786126	AGACATGTCCCAATG[C/G]GAAACGGCCCAGACC	80013
rs779633691	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15847690	ATTGCACAACTCATC[A/G]ATATGGTGAATTCAT	80013
rs779649872	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15846787	GGAGTACAGTGGCGC[A/G]ATCTCGGCTCACTGC	80013
rs779682308	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15856056	GAAAGGAAAAATATA[C/T]ATAAGAGAATGTTAA	80013
rs779710275	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15817139	TTGACATTAAAACAA[C/T]AACAATATAGATTTA	80013
rs779808565	in-del	-/AATA			intron-variant	FAM188A	GRCh38.p7	10:15827546	GACTCCGTCTCAATA[-/AATA]AATAAATAAATAAAT	80013
rs779830550	snp	C/T			missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15834559	TGCCATGTCCATATA[C/T]AGGATCTATCAAGGG	80013
rs779860581	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15794620	CAACAAATTTTCATA[C/T]GCATCTCTCACAACT	80013
rs779870679	snp	G/T	1.91496e-05	0.00309426	intron-variant	FAM188A	GRCh38.p7	10:15833742	AAAGCAATTAAATAT[G/T]AATATAGTTGCCAAA	80013
rs779884420	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15793326	GATTAAACTGAGCCA[A/G]TTATCTAGAGGTGAT	80013
rs779902398	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15818175	GCAACTAAATAGTAC[A/G]GAGCTAGAATTAGGA	80013
rs779905025	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15848328	CTTTCTGTCACATTC[C/T]ATAAGCTAATCATTA	80013
rs779925058	in-del	-/A			intron-variant	FAM188A	GRCh38.p7	10:15811727	CTAATTTGCTTCAGG[-/A]AAAAAAAATAACATA	80013
rs779957787	in-del	-/GTA			intron-variant	FAM188A	GRCh38.p7	10:15801974	AATGAGGAAGATGAC[-/GTA]GAAGAAGCAGGGCCA	80013
rs780010426	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15824731	AGTGTTACAATTAGA[C/T]ACTACATCATCTATT	80013
rs780019229	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15844771	ATATAGCAGTATATG[A/T]GTGTGCCAGCATCTT	80013
rs780028494	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15801402	GCCTGGAAGAGAATG[A/C]TTTCTCTGGATCAGT	80013
rs780037747	snp	A/G	1.65781e-05	0.00287902	intron-variant	FAM188A	GRCh38.p7	10:15834538	AAGAGATTTTAGTTA[A/G]TTACCTGCCATGTCC	80013
rs780067481	in-del	-/CATT			intron-variant	FAM188A	GRCh38.p7	10:15828802	CTAACATGAGACATA[-/CATT]CATTCAGCATTTACT	80013
rs780092961	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15852412	GGACTTAGGATTAGA[A/G]GCAGCAATTTCAATC	80013
rs780122959	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15802335	ACTGACTCATAGATC[C/T]ACATAGCTGGGGAGG	80013
rs780189943	snp	A/G			upstream-variant-2KB	FAM188A	GRCh38.p7	10:15860815	CTTGTATTTTTCAAT[A/G]TTAATTTTGCAAAAC	80013
rs780216470	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15809498	CCATGCCTACAGGGC[A/G]CATTCTGTCTCCATG	80013
rs780231673	snp	A/G	1.65924e-05	0.00288027	intron-variant	FAM188A	GRCh38.p7	10:15786534	CCCAACAGAATAACA[A/G]TGAATATATTTCCTC	80013
rs780288365	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15850058	TTTATCAGTTCCCCA[A/G]ATTAATACTTTTATA	80013
rs780329066	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15789974	GGGGTAGTTTGAAAT[A/G]AGAGTGGTTTTAAAC	80013
rs780364036	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15820679	AATTTGATTATCATA[G/T]GCATATCACCCAGTG	80013
rs780375472	snp	C/T			downstream-variant-500B	FAM188A	GRCh38.p7	10:15777785	TACTATTGAAGGTAA[C/T]GTTCAGTTCTGAAAT	80013
rs780385236	in-del	-/AAAATCAGAAACAACTT	6.7706e-05	0.00581794	intron-variant	FAM188A	GRCh38.p7	10:15789331	TTATCTAGGGGGGAA[-/AAAATCAGAAACAACTT]GAAATAAGAATTTAC	80013
rs780406411	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15833830	GAATTTACAAAGTTA[A/G]GGAAAACCTTACATT	80013
rs780464424	snp	C/T			upstream-variant-2KB	FAM188A	GRCh38.p7	10:15862100	TTATGACAATTCCTA[C/T]CATCATTGTATTTGC	80013
rs780467356	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15833195	AATTTAAAAGTCTCA[A/G]TATTAAATTTGCTCG	80013
rs780473574	in-del	-/ATTA	1.65468e-05	0.00287631	frameshift-variant, nc-transcript-variant	FAM188A	GRCh38.p7	10:15833694	TCCCGTCAGCAGGAG[-/ATTA]ATTAAACTTTGGCTA	80013
rs780499198	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15798278	CTGAAGCGTTACTTC[A/C]ATATTGCTACAAAGT	80013
rs780520362	snp	A/G	1.65581e-05	0.00287728	synonymous-codon, intron-variant, nc-transcript-variant	FAM188A	GRCh38.p7	10:15816913	TTTCAAGTAAGAACC[A/G]ACCTAGAACAAATGT	80013
rs780552362	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15797254	GGAACTAAAACAAGG[C/T]AACCTGTGCAAGCCC	80013
rs780572286	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15841128	CTGAAACTGAAGCAT[A/T]TCATTATTTCTAAAT	80013
rs780614030	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15836448	ACCATTAAAAATGCA[A/T]CCCATATTATTAATA	80013
rs780644394	snp	G/T	1.65457e-05	0.00287621	utr-variant-5-prime, missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15837268	CCCCACATTGAATAC[G/T]GGTCCAAGACAGCAT	80013
rs780670404	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15810722	GGCAAACAGTAGGTG[A/C]CAAAACACAAAAATC	80013
rs780703945	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15833947	TTAACAACTTTATCT[A/T]AGATATATTTAAATG	80013
rs780725464	snp	C/G	1.69596e-05	0.00291196	intron-variant	FAM188A	GRCh38.p7	10:15786683	AAACAGTGGATACCA[C/G]AGGAAAAAAAAAAGC	80013
rs780737879	snp	A/T			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15783774	TTTGATCGTTTCCTT[A/T]ATTACAGGAGTCATT	80013
rs780791107	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15796206	TGTTGTCAACCAGCT[A/G]CAGTATTATGACATT	80013
rs780837115	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15840993	AAGAAAAGAAACAGC[C/T]TGCAATGAGGAGAAA	80013
rs780838769	snp	G/T	8.44859e-05	0.00649891	intron-variant	FAM188A	GRCh38.p7	10:15837333	TCTGGGGGAAAAAAA[G/T]AATTAAGTATTGGTA	80013
rs780854020	in-del	-/CCAG			intron-variant	FAM188A	GRCh38.p7	10:15797206	CATGAGGACTCGATT[-/CCAG]CCTGAAAACCTTATT	80013
rs780855535	in-del	-/G			intron-variant	FAM188A	GRCh38.p7	10:15844764	TTGTACTATATAGCA[-/G]TATATGAGTGTGCCA	80013
rs780885249	in-del	-/AG			intron-variant	FAM188A	GRCh38.p7	10:15800286	AAAATGTATCAAAAC[-/AG]GGGCATACGGACTGT	80013
rs780971668	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15857172	CCCCCTCCTGCCACA[C/T]TAACTTCCTTCTTGT	80013
rs781003295	snp	C/T	1.65853e-05	0.00287964	intron-variant	FAM188A	GRCh38.p7	10:15847821	CAAGTATGAAACGTT[C/T]CAAAATGTCCCTCTA	80013
rs781024218	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15833466	TGGCTCCAAGATTAA[A/T]GGTCTTAACATTATG	80013
rs781069962	snp	A/G			utr-variant-3-prime, nc-transcript-variant	FAM188A	GRCh38.p7	10:15778364	AAAGTTAACAGTGTT[A/G]ACTATCAGATTCTCT	80013
rs781071261	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15815009	TAAGATTTAAAATAT[C/T]GTCATCTTTTATATT	80013
rs781074852	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15791929	GAGATACTAGCTAAA[C/T]TGGACACTGCAGGAA	80013
rs781116817	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15791660	TTAAAATTTTAAAAG[A/T]TTTTTACCAGTTGAA	80013
rs781155133	snp	C/T	1.65217e-05	0.00287412	utr-variant-5-prime, missense, intron-variant, nc-transcript-variant	FAM188A	GRCh38.p7	10:15847928	GCAGATCCCTCTGAT[C/T]CACTAAACACAAACC	80013
rs781156535	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15812737	CCCCAATCCCACTTA[C/T]TACGTGATGTGCATA	80013
rs781230882	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15845307	GTGACAGGTAATGAG[G/T]TCTATGATTGTATTA	80013
rs781267842	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15813352	TGCTCTATTTGTCAT[A/G]TAGAGAATGCTCTTT	80013
rs781272466	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15825941	CCTATCCCATAAAGA[A/C]AATTATAAAATAAAA	80013
rs781286589	snp	A/G	1.76533e-05	0.00297092	intron-variant	FAM188A	GRCh38.p7	10:15833722	TGGCTATTAATAAAT[A/G]TTAAAAAGCAATTAA	80013
rs781293959	snp	A/G	5.00329e-05	0.0050014	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15779153	TGACCTGTTGAACAA[A/G]ATAAAGCCACCAAGG	80013
rs781400472	snp	C/T	7.10543e-05	0.00596004	intron-variant, downstream-variant-500B	FAM188A	GRCh38.p7	10:15782134	CCAGTTGAACACCGA[C/T]GACTACGTGAATTAT	80013
rs781427688	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15853322	AGACCTTTCAGGGGG[C/T]CCACTGGAAGTTACA	80013
rs781452746	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15822364	CGGAGTGGTATGAGA[C/G]TATCTGCCTACAGTG	80013
rs781476636	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15859642	AGATAATAAACCATA[C/T]AAAAAACGGGGATAC	80013
rs781487817	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15801242	AAGCACTAGGATTTA[A/T]GACAGAAAGGAAAAG	80013
rs781516096	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15831075	ATTCTAAAGTCAGCT[C/G]AGAGTGAGTGGGCAG	80013
rs781544497	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15856373	AGCCCAAAGCTCTAA[A/T]TTCAATCAACTACAC	80013
rs781569745	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15806244	GTCTATATTTTCCTC[C/T]TGTGTCTTCCCTCAT	80013
rs781600198	snp	C/T			upstream-variant-2KB	FAM188A	GRCh38.p7	10:15860625	AAGCGGTGGAAGTAG[C/T]TTCTGACCTTTCTGA	80013
rs781645809	snp	A/G	1.80192e-05	0.00300154	intron-variant	FAM188A	GRCh38.p7	10:15841417	TCAGGAAATAAAAAT[A/G]TATCTTACAAGAATG	80013
rs781654490	in-del	-/TGTAATACTTAG			intron-variant	FAM188A	GRCh38.p7	10:15803923	TTCTTCATCCCTAGT[-/TGTAATACTTAG]GAGAAAATTTCAACA	80013
rs781703406	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15808074	ATTTACATACTTGTA[A/G]TAATTCAAATCACTG	80013
rs796101158	snp	G/T			utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	FAM188A	GRCh38.p7	10:15778744	ATCTGAATGCAAAAG[G/T]GATGAACTTTGATGA	80013
rs796119725	in-del	-/AAAAA			intron-variant	FAM188A	GRCh38.p7	10:15816298	AAAAAGAAAAAAAAT[-/AAAAA]AGACAAGAAAAGAAA	80013
rs796197332	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15850869	TGTGATGTCTCCCCC[C/T]GACACCCAGCTTTAA	80013
rs796392686	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15831516	AAACTATACAGAAAA[A/G]AGGTCCACAGCAAGA	80013
rs796397920	in-del	-/A			intron-variant	FAM188A	GRCh38.p7	10:15788074	TATGGAAGAATTTGG[-/A]AAAAAAAAAAACTTT	80013
rs796432324	in-del	-/T			intron-variant	FAM188A	GRCh38.p7	10:15800225	GTAGATACTAGTCTA[-/T]TTTTTTCTACTACCA	80013
rs796472784	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15791103	GTAACCATAACTGTA[C/T]CCGGTCAGTAACTCT	80013
rs796571272	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15855129	ATGCGTTACAGTGAG[A/T]TGCTTTTGTACTTTT	80013
rs796584582	in-del	-/G			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15785587	ATATCACACTGAAGG[-/G]TCTAATGTCGGACAA	80013
rs796691008	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15819458	GCCACTACCATTATA[C/G]GTCTCCCACACTCCA	80013
rs796695627	multinucleotide-polymorphism	GC/TA			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15785010	CCTCCAGATCACTTG[GC/TA]GGGCTTGTTAGACCA	80013
rs796704124	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15850686	AATGACAATGCCGGC[C/G]CAGTACAACATGAAA	80013
rs796750301	in-del	-/AAG			intron-variant	FAM188A	GRCh38.p7	10:15857681	AAAACTGCCCAAAAA[-/AAG]AAGAAGAAAAAAAAC	80013
rs796766131	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15798282	AGCGTTACTTCAATA[A/T]TGCTACAAAGTAAAG	80013
rs796909045	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15849213	GCAAAGGTGAATGAA[C/T]GGAATTCAGCTAAAG	80013
rs796967845	in-del	-/TTA			intron-variant	FAM188A	GRCh38.p7	10:15844554	TTTATCAAAGTTTAC[-/TTA]TTATTTAAATTACAT	80013
rs796971803	in-del	-/AG			intron-variant	FAM188A	GRCh38.p7	10:15836483	CATAGTCCCTAGCAT[-/AG]AGTCAATCAACGCTC	80013
rs796982961	in-del	-/A			intron-variant	FAM188A	GRCh38.p7	10:15788075	TATGGAAGAATTTGG[-/A]AAAAAAAAAACTTTC	80013

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