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
rs1538562	snp	A/G	0.0279526	0.114869	intron-variant	FAM188A	GRCh38.p7	10:15840376	TAATTTTGAACATTT[A/G]AACAGCTATATGATG	80013
rs2297882	snp	A/G	0.456814	0.140456	utr-variant-5-prime, nc-transcript-variant	FAM188A	GRCh38.p7	10:15860304	AGTTCGGACATGATG[A/G]GGAACCGGCGGGCGG	80013
rs2883452	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15859392	TAACCTCATCATCAT[C/T]TTTCCTAAGTCACCT	80013
rs4266971	snp	C/T	0.216349	0.247725	intron-variant	FAM188A	GRCh38.p7	10:15801062	taacaggagaagcag[C/T]ttctgctaacaaaga	80013
rs4387254	snp	C/G	0.479258	0.0997024	intron-variant	FAM188A	GRCh38.p7	10:15808184	TTGTTATTTTAAGGT[C/G]TTAAAAGTCACAGAA	80013
rs4442439	snp	C/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15797384	CATTTACCATCCCTT[C/G]CTAGAAACTTCTTAG	80013
rs4584469	snp	C/G/T			intron-variant	FAM188A	GRCh38.p7	10:15790455	GAGAATAAAGACGAC[C/G/T]TTGGTTGAAGGCACT	80013
rs4748207	snp	G/T	0.0182019	0.0936463	intron-variant	FAM188A	GRCh38.p7	10:15787609	TGTGAGGGTAAGCTA[G/T]GTTTTAAGGTTTATG	80013
rs6602058	snp	A/G	0.451359	0.148171	intron-variant	FAM188A	GRCh38.p7	10:15845984	cctgccactacaccc[A/G]gctaatttttgtatt	80013
rs6602059	snp	C/G	0.249603	0.25	intron-variant	FAM188A	GRCh38.p7	10:15848339	ATTCTATAAGCTAAT[C/G]ATTACATGGCATTgg	80013
rs6602061	snp	C/G	0.306679	0.24349	intron-variant	FAM188A	GRCh38.p7	10:15855395	AGCATTACTTTTCTT[C/G]TCAAGAGTTCTCATA	80013
rs7069213	snp	G/T	0.0345262	0.126772	intron-variant	FAM188A	GRCh38.p7	10:15833999	AAGTTACTTAATATT[G/T]ACAATCtttaaaaat	80013
rs7069225	snp	G/T	0.040671	0.13668	intron-variant	FAM188A	GRCh38.p7	10:15842938	aaGACTGTTCTTTAT[G/T]GCATGCTGCCACCTA	80013
rs7070324	snp	C/T	0.0437281	0.141251	intron-variant	FAM188A	GRCh38.p7	10:15851542	TGGAAAACTCAAACT[C/T]ACCTATAGGTTTCAC	80013
rs7072209	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15848663	aaaaaaaaaaaaaaa[A/G]AAAGAAAAATTAAAT	80013
rs7072213	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15848667	aaaaaaaaaaaGaaa[A/G]AAAAATTAAATGGCA	80013
rs7072683	snp	A/G	0.0119152	0.0762602	intron-variant	FAM188A	GRCh38.p7	10:15843294	ACAATTAAAGCAATA[A/G]TTAGTGAAATGCATT	80013
rs7075115	snp	A/C	0	0	intron-variant	FAM188A	GRCh38.p7	10:15801648	agtagtctgcagaaa[A/C]gatgatatggttatt	80013
rs7081355	snp	A/G	0.239326	0.249772	intron-variant	FAM188A	GRCh38.p7	10:15850332	aacaggatggctgca[A/G]tgttcagggaacaag	80013
rs7086658	snp	A/C	0.209997	0.246779	intron-variant	FAM188A	GRCh38.p7	10:15851907	TCTGTTTACACTTAC[A/C]ATCATTATCTACTGT	80013
rs7090975	snp	A/C	0.289683	0.24683	intron-variant	FAM188A	GRCh38.p7	10:15845370	TTACACAGTATCATG[A/C]TCTAATTTTTATACT	80013
rs7091401	snp	A/C	0.209997	0.246779	intron-variant	FAM188A	GRCh38.p7	10:15845588	cactgcagccctgaa[A/C]tcctgagctcaaaga	80013
rs7094427	snp	G/T	0.232067	0.249356	intron-variant	FAM188A	GRCh38.p7	10:15849447	ATATCATCTTACTGG[G/T]TTTTTTTTTTTTTCT	80013
rs7096756	snp	A/C	0.0463947	0.145069	intron-variant	FAM188A	GRCh38.p7	10:15847073	CCACATTAAATATAT[A/C]TATTTTCAAAACACG	80013
rs7097118	snp	A/C	0.130013	0.219324	intron-variant	FAM188A	GRCh38.p7	10:15841378	TCAATAGATTCATTA[A/C]AACAAAGGAACAAGA	80013
rs7097989	snp	A/G	0.260504	0.249779	intron-variant	FAM188A	GRCh38.p7	10:15841981	CCTGTTGAAACCTCT[A/G]TTTTTTTTCCCTCAC	80013
rs7100782	snp	A/G	0.0383715	0.133092	intron-variant	FAM188A	GRCh38.p7	10:15847374	GAAATCAGTTGTTAC[A/G]AATTTTATTCAGAAA	80013
rs7342102	snp	A/G	0.285519	0.247464	intron-variant	FAM188A	GRCh38.p7	10:15840921	TGAAAAACTTAAGGC[A/G]TAATTAAAATTGCCT	80013
rs7476607	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15856492	TAGTCTTTAGGAGAA[A/C]CAATAAAATAACTGG	80013
rs7895562	snp	C/G	0.00159617	0.0282053	utr-variant-5-prime, nc-transcript-variant	FAM188A	GRCh38.p7	10:15860506	TTTTCCGTACCGGAA[C/G]TGCTGGTGCCACTTC	80013
rs7896076	snp	A/G	0.231189	0.249291	intron-variant	FAM188A	GRCh38.p7	10:15830828	ATATTTTAGCGATGC[A/G]GGCAAGGAAATTCTG	80013
rs7898385	snp	C/T	0.0704125	0.17392	intron-variant	FAM188A	GRCh38.p7	10:15857356	ccccacccagaaCTC[C/T]GTATTTCCTCATCTT	80013
rs7903095	snp	A/G	0.231482	0.249313	intron-variant	FAM188A	GRCh38.p7	10:15837442	GGAAAGTTTTGGGAC[A/G]TTTCTAAATTTTTCA	80013
rs7904049	snp	A/G	0.0696718	0.173152	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15862292	AGCAAGTGAGAGATC[A/G]GGGAAGTAGTACTGA	80013
rs7904872	snp	G/T	0.321769	0.239477	intron-variant	FAM188A	GRCh38.p7	10:15795432	CTACAAGGACTTCAC[G/T]GATACAGCAACTTCC	80013
rs7905215	snp	C/G/T	0.0722113	0.178567	intron-variant	FAM188A	GRCh38.p7	10:15795878	CAGAGGGGTCAACTA[C/G/T]ACCTTCAGTACTCCA	80013
rs7909265	snp	C/T	0.0383715	0.133092	intron-variant	FAM188A	GRCh38.p7	10:15789897	GCTGATGATGACTAC[C/T]TTATGGAAAATGGTC	80013
rs7910149	snp	C/T	0.0376037	0.131863	intron-variant	FAM188A	GRCh38.p7	10:15793706	GCTCTGGAGAAGTGA[C/T]TCAAACCATCAAAAG	80013
rs7912258	snp	C/T	0.32153	0.239548	intron-variant, downstream-variant-500B	FAM188A	GRCh38.p7	10:15782093	AATCGAACGTTGTTA[C/T]ATACTCACATAATTA	80013
rs7913602	snp	C/T	0.255503	0.249939	intron-variant	FAM188A	GRCh38.p7	10:15848582	gagcttgcactgagc[C/T]gagattgtgccactg	80013
rs7913650	snp	C/T	0.0700422	0.173537	intron-variant	FAM188A	GRCh38.p7	10:15857717	CCGCATTTTTTAAAA[C/T]GAACAGGGATTTGTA	80013
rs7920842	snp	G/T	0.288906	0.246954	intron-variant	FAM188A	GRCh38.p7	10:15832518	TGAAGAATAGGATGA[G/T]CTCAATTAAAGAGAG	80013
rs7923528	snp	C/T	0.427271	0.176281	intron-variant	FAM188A	GRCh38.p7	10:15847373	TGAAATCAGTTGTTA[C/T]GAATTTTATTCAGAA	80013
rs7923731	snp	C/T	0.0766824	0.180169	intron-variant	FAM188A	GRCh38.p7	10:15789756	TTCTTGAAGGAATGT[C/T]AGTGATCCACTGATA	80013
rs9783219	snp	C/T	0.110167	0.207236	intron-variant	FAM188A	GRCh38.p7	10:15799054	atgttttgcagggca[C/T]atggtcttagcagca	80013
rs10508494	snp	C/G	0.467946	0.122472	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15779779	GAAAAGTAAAAGAGA[C/G]GTTGAAAGATCAAAC	80013
rs10508495	snp	A/T	0.232067	0.249356	intron-variant	FAM188A	GRCh38.p7	10:15811762	CACTTTCTCCTTATT[A/T]CTAGGGTCTAATACA	80013
rs10690053	in-del	-/CA	0.0333695	0.124785	intron-variant	FAM188A	GRCh38.p7	10:15795004	AAAGTCATTCACTCC[-/CA]GTTTCAACTGTGGTT	80013
rs10716234	in-del	-/T			intron-variant	FAM188A	GRCh38.p7	10:15831693	TTTTTTTTTTTTTTT[-/T]GAGATGGAGTCTCGC	80013
rs10719399	in-del	-/A			intron-variant	FAM188A	GRCh38.p7	10:15848634	GCTAGACTTCATCTC[-/A]AAAAAAAAAAAAAAA	80013
rs10795321	snp	C/G	0.461703	0.132974	intron-variant	FAM188A	GRCh38.p7	10:15819276	TTCCTCCAAGCATCT[C/G]ATAGAAAGTAAATGT	80013
rs10795322	snp	A/G	0.242775	0.249896	intron-variant	FAM188A	GRCh38.p7	10:15819577	tccacaggggagctc[A/G]ggcaatctagctgac	80013
rs10904626	snp	C/T	0.316243	0.241064	intron-variant	FAM188A	GRCh38.p7	10:15801332	CTGCTAAACCCAAGC[C/T]TTGAAGGGAAAAGAT	80013
rs10904627	snp	A/G	0.273049	0.248935	intron-variant	FAM188A	GRCh38.p7	10:15801463	AGTACCCTGCCAGTA[A/G]GAGACCACCTTTTAA	80013
rs10904628	snp	G/T	0.219049	0.248077	intron-variant	FAM188A	GRCh38.p7	10:15809318	GCCTTCATCTAATAA[G/T]AGCTAGTTTTTTCTT	80013
rs10904629	snp	C/T	0.456332	0.141164	intron-variant	FAM188A	GRCh38.p7	10:15812753	TACGTGATGTGCATA[C/T]AGTGAACAAATTGCT	80013
rs10904630	snp	C/T	0.29789	0.24537	intron-variant	FAM188A	GRCh38.p7	10:15816561	TTCAATTGTTTTCTC[C/T]ATAACACAAGTGATT	80013
rs10904631	snp	A/C	0.222035	0.248431	intron-variant	FAM188A	GRCh38.p7	10:15826013	gacaaaaataatgta[A/C]aaataCTGAAGAATT	80013
rs10904632	snp	C/T	0.437259	0.165632	intron-variant	FAM188A	GRCh38.p7	10:15844627	ACATATAAGCTCCTT[C/T]TTAAATACAACTTTT	80013
rs11253647	snp	C/G	0.2768	0.248559	intron-variant	FAM188A	GRCh38.p7	10:15787493	TCAGGTGGTTCTAGT[C/G]AACCACCTTCCTCAG	80013
rs11253649	snp	A/G	0.00795532	0.062565	intron-variant	FAM188A	GRCh38.p7	10:15793284	TTAAGCTGAGTAAGT[A/G]TGCTAGTCTCCCCTT	80013
rs11253650	snp	C/T	0.00279162	0.0372561	intron-variant	FAM188A	GRCh38.p7	10:15797914	ATTTCTAACACATTT[C/T]TCTTTTTCAATTGTC	80013
rs11253651	snp	A/T	0.455977	0.141681	intron-variant	FAM188A	GRCh38.p7	10:15803421	ACATTCAATTGAGAG[A/T]GTTTTACAATCAAGA	80013
rs11253655	snp	C/G			intron-variant	FAM188A	GRCh38.p7	10:15809617	AGGTCCATTTACGTA[C/G]TGCATTTCACCTCAC	80013
rs11253656	snp	A/T	0.235564	0.249583	intron-variant	FAM188A	GRCh38.p7	10:15816621	AAGAAAGAAGAAGAA[A/T]TTATAACTAAATCAT	80013
rs11253658	snp	A/G	0	0	intron-variant	FAM188A	GRCh38.p7	10:15824865	GTAAACACATGCTTA[A/G]ACATCTAGTCTGGAT	80013
rs11253659	snp	A/T	0.0524604	0.153226	intron-variant	FAM188A	GRCh38.p7	10:15833426	CACTAAAGTCATACA[A/T]TTGGGATTTGAACCC	80013
rs11253660	snp	A/G	0.242201	0.249878	intron-variant	FAM188A	GRCh38.p7	10:15845295	TCCTGGTAAATTGTG[A/G]CAGGTAATGAGGTCT	80013
rs11253661	snp	C/T	0.241914	0.249869	intron-variant	FAM188A	GRCh38.p7	10:15845325	TATGATTGTATTATG[C/T]ATTTGGTTCCATTAT	80013
rs11327084	in-del	-/A	0.0788843	0.182262	intron-variant	FAM188A	GRCh38.p7	10:15789399	TGATCAGGTTCCAGG[-/A]AAAAAAAATCGCATA	80013
rs11385214	in-del	-/T			intron-variant	FAM188A	GRCh38.p7	10:15846741	TTTTTTTTTTTTTTT[-/T]GAGACAAAGTCTCGC	80013
rs11410031	in-del	-/T	0	0	intron-variant	FAM188A	GRCh38.p7	10:15832457	GACACTGAAATGAGA[-/T]TTTTTTTTTTCATTG	80013
rs11423907	in-del	-/T	0.287867	0.247116	intron-variant	FAM188A	GRCh38.p7	10:15834973	TGTTAAGGCAACTGA[-/T]TTTTTTTAGATCATG	80013
rs11455489	in-del	-/T			intron-variant	FAM188A	GRCh38.p7	10:15846725	CAGTTTAGGAATGCA[-/T]TTTTTTTTTTTTTTT	80013
rs11455843	in-del	-/T			intron-variant	FAM188A	GRCh38.p7	10:15800231	GTAGATACTAGTCTA[-/T]TTTTTTCTACTACCA	80013
rs11597852	snp	G/T			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15784565	gcctgaccaacaagg[G/T]gaaaccccatctcta	80013
rs11813064	snp	A/G	0.0248432	0.108648	intron-variant	FAM188A	GRCh38.p7	10:15791677	TTTTACCAGTTGAAT[A/G]TCCAGATTGCTAAAA	80013
rs11813535	snp	C/T	0.271162	0.249103	intron-variant	FAM188A	GRCh38.p7	10:15816380	TAAAATTGTGGGAAG[C/T]ATTCCATCTTAAAAG	80013
rs11818243	snp	A/G	0.339429	0.233457	intron-variant, downstream-variant-500B	FAM188A	GRCh38.p7	10:15782086	GTACGGGAATCGAAC[A/G]TTGTTACATACTCAC	80013
rs12218978	snp	C/T	0.31503	0.241394	intron-variant	FAM188A	GRCh38.p7	10:15853957	gcttacagattgttc[C/T]gatgacatcactggt	80013
rs12221218	snp	C/T	0.292008	0.246445	intron-variant	FAM188A	GRCh38.p7	10:15802401	GAGAAGCAAGCACCT[C/T]CTTCACAAGGCAGCA	80013
rs12242143	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15848631	agagctagacttcat[C/T]tcaaaaaaaaaaaaa	80013
rs12243247	snp	A/G	0.238171	0.24972	intron-variant	FAM188A	GRCh38.p7	10:15831339	ATGTGTTATCCAGGA[A/G]AAACCAAGAAGGTTC	80013
rs12243475	snp	A/T	0.186105	0.241697	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15861844	tattttaattaattt[A/T]attttatttCTTCAG	80013
rs12247946	snp	C/T	0.156319	0.231784	intron-variant	FAM188A	GRCh38.p7	10:15856850	TGTGGTCACtctgtc[C/T]gcttcttaccatctc	80013
rs12247963	snp	A/G	0.338296	0.233889	intron-variant	FAM188A	GRCh38.p7	10:15793250	GAACACTTTGAATAG[A/G]CCTGATAACTGCTTC	80013
rs12257572	snp	A/C	0.289683	0.24683	intron-variant	FAM188A	GRCh38.p7	10:15843864	CACAGTGAAGTGTCT[A/C]Cttctcaaagtgtag	80013
rs12258622	snp	C/T	0.308166	0.243139	intron-variant	FAM188A	GRCh38.p7	10:15823077	GAATATTAACTCTGT[C/T]ATTTTTGTGGCCAAC	80013
rs12262809	snp	A/G	0.478603	0.101197	intron-variant	FAM188A	GRCh38.p7	10:15793278	TTCTCTTTAAGCTGA[A/G]TAAGTGTGCTAGTCT	80013
rs12264533	snp	A/G	0.437259	0.165632	intron-variant	FAM188A	GRCh38.p7	10:15827591	aAGCCTTGGATATAA[A/G]AAAATATATCATTAA	80013
rs12265790	snp	C/T	0.261332	0.249743	intron-variant	FAM188A	GRCh38.p7	10:15831289	TTTCTTTTCTAGCAA[C/T]AATCAGCCTGGCAGT	80013
rs12354532	snp	C/G	0	0	intron-variant	FAM188A	GRCh38.p7	10:15812555	TGACAGCTCTCACTA[C/G]TGCTAAATTTAAATT	80013
rs12572784	snp	A/G	0.0944967	0.195752	intron-variant	FAM188A	GRCh38.p7	10:15803314	GGTTCCTAGTATAAA[A/G]ATCTGTAGACTAATC	80013
rs12764431	snp	G/T	0	0	intron-variant	FAM188A	GRCh38.p7	10:15821293	AAGTATTACCAGTTG[G/T]TTTAGTGAAGCATAT	80013
rs12768419	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15843363	GAAAAAATAATGTGT[A/G]CTCCCTTTCTAATCT	80013
rs12769648	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15852318	TTGTTTCTAGGAATA[C/T]CAAGTTCAGTCTCAA	80013
rs12769938	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15843345	TCTTCAATTTTAAAG[A/T]GGGAAAAAATAATGT	80013
rs12770143	snp	A/T	0.5	0	intron-variant	FAM188A	GRCh38.p7	10:15843435	ATTTGACAGGAACTG[A/T]GCAGTTATTTATTCA	80013
rs12770144	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15843440	ACAGGAACTGTGCAG[C/T]TATTTATTCAGAGTA	80013
rs12781122	snp	C/T	0	0	utr-variant-5-prime, missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15841587	TGACAAAGGAGTTCC[C/T]TCTGCTCTTCCTCTA	80013
rs17137842	snp	A/T	0.095934	0.196885	intron-variant	FAM188A	GRCh38.p7	10:15819943	ACATCTAGAAAACCA[A/T]ACAATTCTGGTGAAT	80013
rs17137848	snp	C/T	0.00914312	0.0669923	intron-variant	FAM188A	GRCh38.p7	10:15824479	TGCTTTGGGATCATC[C/T]GTAAGAGTGTAAAGG	80013
rs17395983	snp	A/G	0.287085	0.247234	intron-variant	FAM188A	GRCh38.p7	10:15802851	CTTTTGGTCTCAGTC[A/G]TATACTACTAACAGC	80013
rs28417891	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15814007	AAAGAAAAAGAAAAA[A/G]GAAAAACCCACAGCC	80013
rs28498812	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15814001	AAAAAAAAAGAAAAA[A/G]AAAAAAGAAAAACCC	80013
rs28515530	snp	G/T	0.237303	0.249677	intron-variant	FAM188A	GRCh38.p7	10:15842487	TACTAAAATTTGTTT[G/T]GTATTTCACCTATTA	80013
rs28710863	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15813994	AAAAAAAAAAAAAAA[A/G]GAAAAAGAAAAAAGA	80013
rs33999351	in-del	-/T			intron-variant	FAM188A	GRCh38.p7	10:15781796	TTAAAAATATTTTTT[-/T]CCAGTAAAAAGTCTC	80013
rs34036707	in-del	-/T			intron-variant	FAM188A	GRCh38.p7	10:15797332	CCACTTGACATTTTT[-/T]AACATTTGTAAAATT	80013
rs34064594	in-del	-/T			intron-variant	FAM188A	GRCh38.p7	10:15844629	ATATAAGCTCCTTTT[-/T]AAATACAACTTTTTC	80013
rs34373813	in-del	-/G			intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15783963	TAAAGTGCATAGACT[-/G]CTGTGGTTAGACAGA	80013
rs34429984	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15853552	ATACTTACTGCTGCA[C/G]TCAAAATTACTAATT	80013
rs34579911	in-del	-/C			intron-variant	FAM188A	GRCh38.p7	10:15828765	CAAGGCAAAAAACAG[-/C]ACTAGGAAAAAAATA	80013
rs34722857	in-del	-/A			intron-variant	FAM188A	GRCh38.p7	10:15787968	CTACTTCAAGAAAAA[-/A]CAACCTGATTGAATC	80013
rs34750117	in-del	-/G			intron-variant	FAM188A	GRCh38.p7	10:15817297	AATAACTTTATAAGG[-/G]AAAATAATTATAGTT	80013
rs34767231	in-del	-/C			intron-variant	FAM188A	GRCh38.p7	10:15792299	GGAGTCCAGATCCCC[-/C]AGGGCCTAGCACAGT	80013
rs35013190	in-del	-/G			intron-variant	FAM188A	GRCh38.p7	10:15812430	GATATTTTACTCTAT[-/G]CTTAGCTATCACATT	80013
rs35048587	in-del	-/A			utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	FAM188A	GRCh38.p7	10:15778791	TAAATTTCACACGAA[-/A]GGGGTAAAATAGGAT	80013
rs35133750	in-del	-/A			intron-variant	FAM188A	GRCh38.p7	10:15809361	AAAAACAATTCAAAA[-/A]GTTTAAGTTCTGTAT	80013
rs35140956	snp	C/T	0.0383715	0.133092	intron-variant	FAM188A	GRCh38.p7	10:15809537	TTTGTTCTGCCACAG[C/T]TCAGATGACCTGCTT	80013
rs35491116	in-del	-/T			intron-variant	FAM188A	GRCh38.p7	10:15834980	GCAACTGATTTTTTT[-/T]AGATCATGTAAAAAC	80013
rs35590475	in-del	-/A			intron-variant	FAM188A	GRCh38.p7	10:15853494	TCACTGTCCTAAAAA[-/A]CACCCCCATACCCTC	80013
rs35656374	in-del	-/T			intron-variant	FAM188A	GRCh38.p7	10:15792928	CATGGTTAATGTATT[-/T]GAGTGCTGACTAATC	80013
rs35671275	in-del	-/T			intron-variant	FAM188A	GRCh38.p7	10:15781796	TTTAAAAATATTTTT[-/T]CCAGTAAAAAGTCTC	80013
rs35682566	in-del	-/A			intron-variant	FAM188A	GRCh38.p7	10:15820169	GTGGTCAAGAAAAAA[-/A]GTCTCTGAGGTACGA	80013
rs35802848	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15787274	AGCCCTTACAATGCA[A/G]GTGTACCAAGGCTGG	80013
rs35810825	in-del	-/TT/TTT			intron-variant	FAM188A	GRCh38.p7	10:15798480	TTTTTTTTTTTTTTT[-/TT/TTT]AAATACTCTGCTAGT	80013
rs35836018	in-del	-/AAAC			intron-variant	FAM188A	GRCh38.p7	10:15798797	AACAAACAAACAAAC[-/AAAC]AAAAAACCACTATGC	80013
rs41289287	snp	C/G	0.0183018	0.0938957	intron-variant	FAM188A	GRCh38.p7	10:15789362	TGAAATAAGAATTTA[C/G]TTCAAGAAATGCTAT	80013
rs41289289	snp	A/G	0.0107246	0.0724382	intron-variant	FAM188A	GRCh38.p7	10:15814701	CACTGGCTGCCATGG[A/G]ACACGCAGAAAACAG	80013
rs55753158	in-del	-/TCT			cds-indel, nc-transcript-variant	FAM188A	GRCh38.p7	10:15778253	TGTAATAACAGATCT[-/TCT]CATGCATTTATCGTG	80013
rs55753523	snp	C/T	0.0154538	0.0865337	intron-variant	FAM188A	GRCh38.p7	10:15836348	CTTGATTCCATCTAA[C/T]AGGTTCAGACAGAAG	80013
rs55760037	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15826394	ACTGGGGTAGAATCA[A/G]GTATATGGATTCAGG	80013
rs55802471	snp	C/T	0.00597247	0.0543191	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15784062	TCTAATCTTCAATTT[C/T]CTCATTGTCAAAAAA	80013
rs55857382	snp	C/G	0.00597247	0.0543191	intron-variant	FAM188A	GRCh38.p7	10:15781967	TGAAGTCCAATGTCA[C/G]TTTCCAATGCAGACT	80013
rs55956244	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15785631	TTCATGAAGGCTTTA[A/G]GACCAAAGTTTTAAG	80013
rs56002039	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15796592	TTTCAAATATTCGAA[A/G]ATAAAATCCAGAGAT	80013
rs56070000	in-del	-/T			intron-variant	FAM188A	GRCh38.p7	10:15831013	GGAAAGATATATAGT[-/T]CTTCTAAAACAGGAA	80013
rs56087004	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15816432	TGAATTATTAATAGA[C/T]TTTAAAATTTTTTCA	80013
rs56153759	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15806448	GGGCCCCCAACCAAT[C/T]CTACCTCGTTTTCTA	80013
rs56332799	in-del	-/A			intron-variant	FAM188A	GRCh38.p7	10:15827198	AAAAAAAAAAAAAAA[-/A]GCCCAAATAGAAGCC	80013
rs56379461	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15856329	TATCTTTTTTTCATA[C/T]TACGTAACAAAAATT	80013
rs56392801	snp	A/G	3.30764e-05	0.00406659	missense, intron-variant, nc-transcript-variant	FAM188A	GRCh38.p7	10:15786601	AATGGGCCCAATAAT[A/G]TGATTCCTAATCCTT	80013
rs57020273	in-del	-/A			intron-variant	FAM188A	GRCh38.p7	10:15828592	TAAAAAAAAAAAAAA[-/A]TTAACAGATGCCTAA	80013
rs57043351	snp	C/T	0.0441095	0.141807	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15783765	AAAAATCAATTTGAT[C/T]GTTTCCTTAATTACA	80013
rs57205297	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15798672	GTTAACCCAGCTACT[C/T]GGGAGGCTGAGGCAG	80013
rs57324199	snp	C/T	0.0146672	0.084371	intron-variant	FAM188A	GRCh38.p7	10:15825977	CATCAAATAAGCATA[C/T]AAAAATAAATAAACA	80013
rs57432492	in-del	-/T			intron-variant	FAM188A	GRCh38.p7	10:15819007	AAATCTATCTTTTTT[-/T]AAAAAAGTAGAGTCA	80013
rs57565966	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15842411	TGAATATAGTATAAG[A/G]AATAGTATAAATTTT	80013
rs58193134	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15805690	AAATACAACTGGGAG[A/T]GACATTATGCTAGCT	80013
rs58353418	snp	C/T	0.00478085	0.0486577	downstream-variant-500B	FAM188A	GRCh38.p7	10:15777728	AATTGTGTGTGTGTA[C/T]GAAAGAAAACAAAAC	80013
rs58992930	in-del	-/CAAA/CAAACAAT	0.0352966	0.128072	intron-variant	FAM188A	GRCh38.p7	10:15798800	AAACAAACAAACAAA[-/CAAA/CAAACAAT]AAACCACTATGCCAA	80013
rs59124459	in-del	-/G	0.21695	0.247806	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15785585	GGATATCACACTGAA[-/G]GGTCTAATGTCGGAC	80013
rs59260806	snp	C/G	0.0189856	0.0955633	intron-variant	FAM188A	GRCh38.p7	10:15850729	TTCTAATTTTGCCCT[C/G]GTCCTGTGATCTCAC	80013
rs61145026	snp	C/T	0.0333695	0.124785	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15779546	TGCTGCCTAATGAAA[C/T]GGAGAGCTATAAAAG	80013
rs61843952	snp	G/T	0.5	0	intron-variant	FAM188A	GRCh38.p7	10:15788008	AACTTCATGATTCAA[G/T]GTACGTTTTCCATCT	80013
rs61843953	snp	A/G	0	0	intron-variant	FAM188A	GRCh38.p7	10:15798835	GAAAGAAATTAAAGT[A/G]AACCTTAATGAAAAG	80013
rs61844793	snp	C/G/T	0.0023933	0.0345097	intron-variant	FAM188A	GRCh38.p7	10:15814036	CCAAAACTGCTTGCT[C/G/T]AAATGCAGAAATGTT	80013
rs61844794	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15821292	AAAGTATTACCAGTT[A/G]TTTTAGTGAAGCATA	80013
rs61844795	snp	A/G	0.5	0	intron-variant	FAM188A	GRCh38.p7	10:15832248	AGTATCAAGGACAGA[A/G]GGCCAAGTGGGATGA	80013
rs61844796	snp	A/T	0.5	0	intron-variant	FAM188A	GRCh38.p7	10:15845673	CCAGCTAATTTTTTC[A/T]ATTTTTTTTTTTTTT	80013
rs61844797	snp	A/G	0.0349115	0.127424	intron-variant	FAM188A	GRCh38.p7	10:15852780	AAACTACAGTTGGCC[A/G]TTCATATCCATAGGT	80013
rs61844798	snp	C/T	0.00953873	0.0683987	intron-variant	FAM188A	GRCh38.p7	10:15853401	TGACATTCACAGTGA[C/T]GGTACAAAAGCTATG	80013
rs61844799	snp	A/C	0	0	intron-variant	FAM188A	GRCh38.p7	10:15856431	AAGAAAAAAAAAACC[A/C]ACCCACTGTACTGCT	80013
rs67946495	in-del	-/CA			intron-variant	FAM188A	GRCh38.p7	10:15795005	AAGTCATTCACTCCG[-/CA]TTTCAACTGTGGTTC	80013
rs71493234	snp	A/C	0.5	0	intron-variant	FAM188A	GRCh38.p7	10:15794607	TCTAAAAGAAATACA[A/C]CAAATTTTCATATGC	80013
rs71493236	snp	A/G	0.0414363	0.137845	utr-variant-5-prime, nc-transcript-variant	FAM188A	GRCh38.p7	10:15860426	AGGTGAGGCAGGAAA[A/G]AAGAAGGGGCTGAGA	80013
rs71881059	in-del	-/TT			intron-variant	FAM188A	GRCh38.p7	10:15798465	CTAAGTGCCAAGTGT[-/TT]TTTTTTTTTTTTTTT	80013
rs72001657	in-del	-/A	0.234692	0.249531	intron-variant	FAM188A	GRCh38.p7	10:15816581	CACAAGTGATTTCTG[-/A]AAAAAATCAAAAGCT	80013
rs72781875	snp	C/T	0.0475351	0.146656	intron-variant	FAM188A	GRCh38.p7	10:15814837	AAAAAGAAGGGCCTA[C/T]TTCACTCTTGGGAAC	80013
rs72781876	snp	A/G	0.0535932	0.154675	intron-variant	FAM188A	GRCh38.p7	10:15819732	AGAGTTTTGCCTTTC[A/G]CCTATCCAAGTGTTA	80013
rs72781878	snp	C/T	0.0425829	0.139564	intron-variant	FAM188A	GRCh38.p7	10:15820591	CACAATTAAAGTCAC[C/T]GAAGATAAAAGTCAC	80013
rs72781879	snp	G/T	0.0944967	0.195752	intron-variant	FAM188A	GRCh38.p7	10:15821434	TTCTGCCCCTCCTCC[G/T]ACAAAAATAACAACA	80013
rs72781880	snp	C/G	0.0581099	0.160244	intron-variant	FAM188A	GRCh38.p7	10:15821538	GATAGGAAGGAAGAA[C/G]AGAGCGGTACTGAAC	80013
rs72781882	snp	A/C	0.0520825	0.152737	intron-variant	FAM188A	GRCh38.p7	10:15837999	ATGAAAAAGCTTTTT[A/C]ATGTTTTTGAAAAGC	80013
rs72781883	snp	G/T	0.0134861	0.0810011	intron-variant	FAM188A	GRCh38.p7	10:15845270	CTTCTTTATTCCTGG[G/T]GTGACAAATTCCTGG	80013
rs72781886	snp	A/C	0.245631	0.249962	intron-variant	FAM188A	GRCh38.p7	10:15849354	CAAATGGGCGGCAGG[A/C]AAGATGACAAGTGGT	80013
rs72781887	snp	A/T	0.0123036	0.0774623	intron-variant	FAM188A	GRCh38.p7	10:15857448	CCACCCTACTGACTC[A/T]CAACTGTAAGAGCTT	80013
rs73589628	snp	A/G	0.0287284	0.116357	intron-variant	FAM188A	GRCh38.p7	10:15791090	GATATTCTGAAGTGT[A/G]ACCATAACTGTACCC	80013
rs73589630	snp	C/T	0.0150606	0.0854603	intron-variant	FAM188A	GRCh38.p7	10:15807203	ACTCACAGTAAACTA[C/T]TACCATGTATTATTA	80013
rs73589635	snp	A/G	0.0448719	0.142907	intron-variant	FAM188A	GRCh38.p7	10:15843811	ACTTCCCCTTAAGCG[A/G]GTCAACGATGTTACA	80013
rs73589639	snp	A/C	0.0193772	0.0965046	intron-variant	FAM188A	GRCh38.p7	10:15855106	ACAGGTGGGGCTTTC[A/C]GTTGGAAATGCGTTA	80013
rs73589640	snp	A/C	0.0154538	0.0865337	intron-variant	FAM188A	GRCh38.p7	10:15857705	AAAAAAAACACCCCG[A/C]ATTTTTTAAAACGAA	80013
rs74124360	snp	A/G	0.0123036	0.0774623	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	FAM188A	GRCh38.p7	10:15778789	TAGTAAATTTCACAC[A/G]AAGGGGTAAAATAGG	80013
rs74124361	snp	A/G	0.0130921	0.0798413	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15783619	AAATAATTTGAGAAG[A/G]AATCATATAGTACTA	80013
rs74126618	snp	C/T	0.000242202	0.0110019	intron-variant	FAM188A	GRCh38.p7	10:15789221	TCTTTTTGAGTTGGC[C/T]AAATAACACTTCCTA	80013
rs74126619	snp	A/G	0.0123036	0.0774623	intron-variant	FAM188A	GRCh38.p7	10:15790832	GAGGATCAACCTTTC[A/G]GGTGAGGGATGCTCA	80013
rs74126620	snp	C/T	0.5	0	intron-variant	FAM188A	GRCh38.p7	10:15812321	TCTCAATTATTCATG[C/T]GTTAAATATTACTCA	80013
rs74126622	snp	C/T	0.0162398	0.0886349	intron-variant	FAM188A	GRCh38.p7	10:15815687	TGATGATGATGATGA[C/T]GATGACCACAGCTAA	80013
rs74126623	snp	C/T	0.0150606	0.0854603	intron-variant	FAM188A	GRCh38.p7	10:15828119	ACTAAAATATACATC[C/T]CATAAAAACTTGTAC	80013
rs74126624	snp	C/T	0.0267878	0.112589	intron-variant	FAM188A	GRCh38.p7	10:15847203	ACAGTAAACTGAGAA[C/T]TCAATTCTTGGTTTT	80013
rs74228708	snp	C/T	0.119281	0.213102	intron-variant	FAM188A	GRCh38.p7	10:15802198	TATGCAGGGGGTTAG[C/T]ACCCCAACTCCCATG	80013
rs74366732	snp	C/T	0.00676609	0.0577691	intron-variant	FAM188A	GRCh38.p7	10:15821543	GAAGGAAGAAGAGAG[C/T]GGTACTGAACCATAG	80013
rs74396956	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15822838	GCAGGGAATAAAAAT[G/T]TGATAATAATAAAGT	80013
rs74399423	snp	A/G	0.0197687	0.0974348	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15784263	TATTCTTATTTAAAC[A/G]AATGGTCTTGAAAAG	80013
rs74402455	snp	A/G	0.0107246	0.0724382	intron-variant	FAM188A	GRCh38.p7	10:15807308	GCCACAAGAAGGAAG[A/G]AAGTTGGAAGAAAGA	80013
rs74408446	snp	C/T	0.0146672	0.084371	intron-variant	FAM188A	GRCh38.p7	10:15797932	TTTTTCAATTGTCTC[C/T]GTTAGACTGTTGAAA	80013
rs74524642	snp	G/T	0	0	intron-variant	FAM188A	GRCh38.p7	10:15846741	TTTTTTTTTTTTTTT[G/T]GAGACAAAGTCTCGC	80013
rs74605863	snp	C/T	0.077417	0.180873	intron-variant	FAM188A	GRCh38.p7	10:15791589	GGGAAACGGCTAGCA[C/T]GTACATACTGTAATG	80013
rs74626242	snp	A/T	0.0271762	0.113356	intron-variant	FAM188A	GRCh38.p7	10:15806038	AATGTCAGTAGTCAC[A/T]CACTCCTCCTACCCA	80013
rs74656033	snp	A/G	0.0178098	0.0926698	intron-variant	FAM188A	GRCh38.p7	10:15855159	TAATATTAAAAGCCC[A/G]TGGAGTGAATTCTAA	80013
rs74666225	snp	C/T	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15804775	AAGTCAATTACATCA[C/T]CTCAAAACACAGAAC	80013
rs74685359	snp	A/G	0.5	0	intron-variant	FAM188A	GRCh38.p7	10:15796477	TAAAAATGTAGCATG[A/G]AAAAAAAAAACAAAA	80013
rs74756426	snp	C/T	0.0667028	0.170006	intron-variant	FAM188A	GRCh38.p7	10:15858809	AATGGAAGTAAATTT[C/T]TTCTTAGTCTTTCAC	80013
rs74757643	snp	C/T	0.0287284	0.116357	intron-variant	FAM188A	GRCh38.p7	10:15853460	ACATCGAGACAGTAA[C/T]ATCAAGCTGTCCTAG	80013
rs74776637	snp	A/G	0.105214	0.203807	intron-variant	FAM188A	GRCh38.p7	10:15805195	TTTTCTTGAAGTTAG[A/G]CGACGTTCTTGGAGG	80013
rs74797257	snp	C/T	0.0158469	0.0875917	intron-variant	FAM188A	GRCh38.p7	10:15805996	CAAATTCCTTTTTGC[C/T]ATCACCACGTGCAGA	80013
rs74843946	snp	A/G	0.00572587	0.0531991	synonymous-codon, downstream-variant-500B, nc-transcript-variant	FAM188A	GRCh38.p7	10:15779079	TTTAATAGGAGTGTC[A/G]TCTGTCTGTAGCATG	80013
rs74925997	snp	C/T	0.0107246	0.0724382	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15784468	ATGTTTACTGGGCCT[C/T]GTGAGGTGGCTCATA	80013
rs74963711	snp	C/G	0.0111196	0.0737302	intron-variant	FAM188A	GRCh38.p7	10:15858824	TTTCTTAGTCTTTCA[C/G]AGTATTTTAGAGCTG	80013
rs74964942	snp	C/T	0.0111196	0.0737302	intron-variant	FAM188A	GRCh38.p7	10:15832134	CGAGAATCCGGAGAA[C/T]GCGTAGAAAGATGAA	80013
rs74988810	snp	A/C	0.00716266	0.059414	intron-variant	FAM188A	GRCh38.p7	10:15846368	CTAATTTACATATGG[A/C]CATAACAAGGAATCT	80013
rs75013318	snp	C/T	0.046775	0.145601	intron-variant	FAM188A	GRCh38.p7	10:15813562	CTCAAGGAGAATGTC[C/T]GCCTCCATTAAGAAC	80013
rs75014911	snp	A/T	0.0329836	0.124112	intron-variant	FAM188A	GRCh38.p7	10:15788635	CTTAAGAAGAGTTAT[A/T]TTTTCATGGATAATA	80013
rs75054458	snp	A/T	0.0777841	0.181223	intron-variant	FAM188A	GRCh38.p7	10:15788939	TACTGAAGATACTAA[A/T]GTCACATAAAATTTT	80013
rs75088045	snp	G/T	0.23846	0.249734	intron-variant	FAM188A	GRCh38.p7	10:15856100	CAACAAAAAAACTTT[G/T]AAACGATGTGATCCA	80013
rs75091190	snp	C/G	0.00517822	0.0506191	intron-variant	FAM188A	GRCh38.p7	10:15822626	GGACTCGTGTGAAGA[C/G]GTAACATGAGTTTGG	80013
rs75136693	snp	C/T	0.5	0	intron-variant	FAM188A	GRCh38.p7	10:15816446	ATTTTAAAATTTTTT[C/T]AAAGGAGATGCTGTA	80013
rs75156444	snp	C/T	0.0696718	0.173152	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15862181	CTGCCTATTCATAAT[C/T]CTAGCATGGGGCCTT	80013
rs75290469	snp	A/G	0.077417	0.180873	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15780810	AGAAGCTTGTCACAA[A/G]CATGATTTGAAAACT	80013
rs75332332	snp	G/T			intron-variant	FAM188A	GRCh38.p7	10:15788977	GGGGAAGTGTTTGCA[G/T]AGAAACTTTTTAAAG	80013
rs75342153	snp	A/C			intron-variant	FAM188A	GRCh38.p7	10:15797829	TTATTCCTCAGTTCC[A/C]TTTATCACTCCCAAA	80013
rs75452554	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15810454	AATAATACGGGTGGT[C/T]TGAATTGGTCAGGTA	80013
rs75517263	snp	C/T	0.0119091	0.0762411	intron-variant	FAM188A	GRCh38.p7	10:15800488	GGCGCTAATCATCTC[C/T]GCATGTGCAGCCCAT	80013
rs75649528	snp	A/G	0.0146672	0.084371	intron-variant	FAM188A	GRCh38.p7	10:15830834	TAGCGATGCGGGCAA[A/G]GAAATTCTGCTGGTG	80013
rs75720422	snp	A/G/T			intron-variant	FAM188A	GRCh38.p7	10:15814400	TTAGGGGATATAAAC[A/G/T]TCACTGGAACCCAAA	80013
rs75816613	snp	C/G	0.5	0	intron-variant	FAM188A	GRCh38.p7	10:15830956	CAGGGAAGAGAATCA[C/G]ATTTAATAGCAGAGA	80013
rs75829949	snp	C/T	0.078151	0.181571	intron-variant	FAM188A	GRCh38.p7	10:15804571	TAACTTCAAGAATGA[C/T]TGCACATATATAAAT	80013
rs75872946	snp	C/T	0.0704125	0.17392	intron-variant	FAM188A	GRCh38.p7	10:15858290	TTGAAATGGTACTGA[C/T]GGAACTAATCCTGTT	80013
rs75890684	in-del	-/AA			intron-variant	FAM188A	GRCh38.p7	10:15818328	GAAGTAAAAAAAAAA[-/AA]CAAACAAACAAAGGA	80013
rs75928440	snp	A/C	0.0295035	0.117819	intron-variant	FAM188A	GRCh38.p7	10:15813149	CCAAAACTACTCCCA[A/C]TACCAATTTTTAACA	80013
rs76018646	snp	C/G	0.02016	0.0983543	intron-variant	FAM188A	GRCh38.p7	10:15832308	TATTGCTTCCCTAAT[C/G]ATATGAGATAAGATA	80013
rs76103500	snp	C/T	0.029116	0.117091	intron-variant	FAM188A	GRCh38.p7	10:15787806	GAGTCTGAGTAAGGC[C/T]GGGAAGTTATGATGA	80013
rs76149530	snp	C/G	0.0463947	0.145069	intron-variant	FAM188A	GRCh38.p7	10:15818423	AATGCATAAATAAGT[C/G]TCATCACTTTGGACA	80013
rs76194674	snp	C/G/T	0.0770498	0.180522	intron-variant	FAM188A	GRCh38.p7	10:15788625	CATGTATCCACTTAA[C/G/T]AAGAGTTATTTTTTC	80013
rs76250424	snp	A/C	0.0287284	0.116357	intron-variant	FAM188A	GRCh38.p7	10:15822164	GGTAGCAGTGACTCC[A/C]CTTGCCTAATACTTA	80013
rs76291043	snp	C/T	0.00636936	0.0560724	intron-variant	FAM188A	GRCh38.p7	10:15853700	TCAAGGAAAAGTATA[C/T]GTGTAATTTTTTTAA	80013
rs76476157	snp	A/G	0.0839998	0.186933	intron-variant	FAM188A	GRCh38.p7	10:15797757	TCTTATGCCAAAGCT[A/G]GGACTGCAGTGTTGG	80013
rs76518753	snp	A/G	0.0704125	0.17392	intron-variant	FAM188A	GRCh38.p7	10:15854670	GAAAGTGTTAATTCC[A/G]AAAAACATAAGGAAA	80013
rs76561133	snp	C/G	0.5	0	intron-variant	FAM188A	GRCh38.p7	10:15848416	GAGGCGGGCGGATCA[C/G]GAGGTCAGGAGATCG	80013
rs76572448	snp	C/T	0.251859	0.249993	intron-variant	FAM188A	GRCh38.p7	10:15855640	TTTTTCAATCTCTTG[C/T]TTTCATATTACTTAC	80013
rs76598581	snp	C/G	0.0763149	0.179815	intron-variant	FAM188A	GRCh38.p7	10:15806722	GATCGTCAACCTTTG[C/G]TTTCATCTTAATATC	80013
rs76749489	snp	C/T	0.0310518	0.120672	intron-variant	FAM188A	GRCh38.p7	10:15820729	AGGAACGCTGTCTGA[C/T]GAAAAAGAGGATCAA	80013
rs76751842	snp	A/G	0.0158469	0.0875917	intron-variant	FAM188A	GRCh38.p7	10:15820137	TATTAAATATTGTGG[A/G]AAAGAATATCTGAGG	80013
rs76787948	snp	A/C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15853580	ATTTTATTGTATCTT[A/C/G]ATCTTGAATACAATG	80013
rs76809914	snp	C/T	0.00914312	0.0669923	downstream-variant-500B	FAM188A	GRCh38.p7	10:15777836	ATTATCTGCTTTACA[C/T]GTGGCTTTACACGTG	80013
rs76865873	snp	A/G	0.0700422	0.173537	intron-variant	FAM188A	GRCh38.p7	10:15858039	GTGCCTGTTCCCACA[A/G]TCCCAAAGGACTGCC	80013
rs76916684	snp	A/G	0.00279162	0.0372561	intron-variant	FAM188A	GRCh38.p7	10:15819347	ACTGTAGCGTAATAT[A/G]GTTTTTCAAAAAATG	80013
rs76946801	snp	C/T	0.5	0	intron-variant	FAM188A	GRCh38.p7	10:15855563	TCACAGAAAAATCTT[C/T]CTCATTTTCACATTT	80013
rs77014947	snp	C/T	0.00199481	0.0315187	intron-variant	FAM188A	GRCh38.p7	10:15794208	CCAGCCTCTGCTAAA[C/T]GGAAACTGTATGTAA	80013
rs77049559	snp	A/G	0.00651248	0.0566906	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	FAM188A	GRCh38.p7	10:15778987	CTTATAAATACTTAG[A/G]CAAATTAATTTAGTG	80013
rs77093688	snp	A/C	0.0352966	0.128072	intron-variant	FAM188A	GRCh38.p7	10:15808464	AACTGTCCAGTTTTT[A/C]AACACCTAAGAGAGA	80013
rs77192937	snp	A/C	0	0	intron-variant	FAM188A	GRCh38.p7	10:15856428	AAAAAGAAAAAAAAA[A/C]CCCACCCACTGTACT	80013
rs77209351	snp	C/T	0.00914312	0.0669923	intron-variant	FAM188A	GRCh38.p7	10:15807365	TCAGCGGACACAATA[C/T]GAATGGTGGAAGGTT	80013
rs77224872	snp	A/C	0.0298908	0.118541	intron-variant	FAM188A	GRCh38.p7	10:15836930	GGGGTCAAGTGCTAC[A/C]CGGAAGGATCAAAGG	80013
rs77301332	snp	A/G	0.0189856	0.0955633	intron-variant	FAM188A	GRCh38.p7	10:15858922	GATTAGGTAACTGAC[A/G]TAATTGAATGTGAAA	80013
rs77304738	snp	A/G	0.0209421	0.100162	intron-variant	FAM188A	GRCh38.p7	10:15803842	CCCACCACACACACA[A/G]AAAACCCCACGAATG	80013
rs77358725	snp	C/T	0.0349115	0.127424	intron-variant	FAM188A	GRCh38.p7	10:15787850	AGGGTCATTTGTGTT[C/T]AATTCATTTAATCCT	80013
rs77600078	snp	A/T	0.0275645	0.114116	intron-variant	FAM188A	GRCh38.p7	10:15851530	TAACCATTTCTCTGG[A/T]AAACTCAAACTTACC	80013
rs77603170	snp	A/C	0.00755907	0.0610114	intron-variant	FAM188A	GRCh38.p7	10:15788715	AACATAACAGTGAGA[A/C]TGAAGACAATGACAG	80013
rs77661298	in-del	-/TG	0.00279162	0.0372561	intron-variant	FAM188A	GRCh38.p7	10:15857214	ACCAAGTGTATTTTC[-/TG]TGAAGTTTTTTATAA	80013
rs77694765	snp	A/G	0.5	0	intron-variant	FAM188A	GRCh38.p7	10:15786696	CAGAGGAAAAAAAAA[A/G]GCTGCTTTTCTTTCA	80013
rs77696579	snp	A/G	0.00318978	0.0398085	intron-variant	FAM188A	GRCh38.p7	10:15817295	GATAATAACTTTATA[A/G]GGAAAATAATTATAG	80013
rs77713269	snp	C/T	0.00835141	0.0640778	intron-variant	FAM188A	GRCh38.p7	10:15855840	TATCTTTCAGGGTTG[C/T]TGCAAAGATTAGGTA	80013
rs77721394	snp	A/G	0.00597247	0.0543191	intron-variant	FAM188A	GRCh38.p7	10:15858246	CTAACTGCACCCTGT[A/G]AACGAAAAAAAGAAA	80013
rs77835927	snp	C/T	0.00716266	0.059414	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15786429	CTGTCTGGGAAGGTT[C/T]CCATGTAACGGTGTT	80013
rs77859374	snp	A/G	0.5	0	intron-variant	FAM188A	GRCh38.p7	10:15800595	ATACTGTAACTCTTG[A/G]AAAAAAACCATGGAA	80013
rs78023003	snp	C/T	0.0166325	0.0896639	intron-variant	FAM188A	GRCh38.p7	10:15799133	GGTGACTTTATTTGG[C/T]CTGAGGGCCATTTGC	80013
rs78121905	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15815034	TATATTCAACACTTT[C/T]AGTTTCATATAATTA	80013
rs78185952	snp	A/G	0.0984431	0.198823	intron-variant	FAM188A	GRCh38.p7	10:15805795	CACATTCCAGGCAGA[A/G]GCTACTCCTTCAGCC	80013
rs78219000	snp	A/T	0.0158469	0.0875917	intron-variant	FAM188A	GRCh38.p7	10:15802505	GAACAGCATGGGGGA[A/T]ACAGCCCCCATGACT	80013
rs78300736	snp	G/T	0.0283406	0.115616	intron-variant	FAM188A	GRCh38.p7	10:15848697	ATTGTAGACAGTACA[G/T]GTGTTTATATTGGCT	80013
rs78322551	snp	A/G	0.0267878	0.112589	intron-variant	FAM188A	GRCh38.p7	10:15781937	GTGTATTTAGTCATG[A/G]TGAAACTACTGCTCT	80013
rs78506922	snp	A/G	0.0752113	0.178743	intron-variant	FAM188A	GRCh38.p7	10:15853127	GGCAGAAGGGAAAAA[A/G]GAATGATAGTTTGAA	80013
rs78541131	snp	C/T	0.0707826	0.174302	intron-variant	FAM188A	GRCh38.p7	10:15792578	CAATTCTAGAGAATG[C/T]CTAGGGAGTGGTGTA	80013
rs78544100	snp	A/G	0.00755907	0.0610114	intron-variant	FAM188A	GRCh38.p7	10:15825885	CACAAAAAACCAAGA[A/G]ACTTCTGGGTTTCTG	80013
rs78547190	snp	A/C/G	0.00252485	0.0354412	intron-variant	FAM188A	GRCh38.p7	10:15786653	TGAGATTTATACTAC[A/C/G]GGGAGAAAGAAGAAA	80013
rs78551795	snp	C/T	0.0146672	0.084371	intron-variant	FAM188A	GRCh38.p7	10:15810580	CCTCCCGACCCCCAA[C/T]TTATCAAGTAATAAC	80013
rs78573102	snp	A/G	0.0248432	0.108648	intron-variant	FAM188A	GRCh38.p7	10:15843042	TAACCCCTGGTTAGA[A/G]AGCCAAATTTGGAAA	80013
rs78588660	snp	C/T	0.0298908	0.118541	intron-variant	FAM188A	GRCh38.p7	10:15798491	TTTTTAAATACTCTG[C/T]TAGTGGTTGGGCACG	80013
rs78589880	snp	A/G	0.0456336	0.143994	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15783175	AGGGGATGGGAGGTG[A/G]AGACCTCCCAGTGCT	80013
rs78656402	snp	A/T	0.00636936	0.0560724	intron-variant	FAM188A	GRCh38.p7	10:15842258	TTCAAAAATTTTATG[A/T]TACAAGGAGGTTTCT	80013
rs78709304	snp	A/T	0.00279162	0.0372561	intron-variant	FAM188A	GRCh38.p7	10:15830111	CTTGTTGAATAAAGT[A/T]ACATCAGAAAACATT	80013
rs78791207	snp	C/T	0.0337553	0.125452	intron-variant	FAM188A	GRCh38.p7	10:15812591	ACTAAGCAGTTTCTA[C/T]GTGGTGCATCAGTCT	80013
rs78961390	snp	C/T	0.0670745	0.170406	intron-variant	FAM188A	GRCh38.p7	10:15859545	TGTACTAAGACTCTT[C/T]ATGTAAGTAAAAGTC	80013
rs78983164	snp	A/T	0.0115144	0.0749975	intron-variant	FAM188A	GRCh38.p7	10:15804095	AAGCAGTTCTTTACA[A/T]TAGTCTGATATAATC	80013
rs79172328	snp	C/T	0.0700422	0.173537	intron-variant	FAM188A	GRCh38.p7	10:15856766	CCAAATAAGTCAAAA[C/T]GTTTTTATTTATACA	80013
rs79185357	snp	G/T	0.5	0	intron-variant	FAM188A	GRCh38.p7	10:15849445	TAATATCATCTTACT[G/T]GTTTTTTTTTTTTTT	80013
rs79229604	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15831184	AGGAGTAGAAAAAAG[A/G]GTTACAATGTGCAGT	80013
rs79240279	snp	G/T	0.0718919	0.175435	intron-variant	FAM188A	GRCh38.p7	10:15830875	GAGAAAGAGGTTTGT[G/T]GCCTGGTCGTTACAC	80013
rs79246501	snp	C/G	0.0341408	0.126114	intron-variant	FAM188A	GRCh38.p7	10:15813280	AGCCCTTGTCTTTCA[C/G]TTTGTTCTCACCCAA	80013
rs79396886	snp	G/T	0.00835141	0.0640778	intron-variant	FAM188A	GRCh38.p7	10:15844907	TGAGGGTGAGCATCC[G/T]GATTATTTGGCTGTA	80013
rs79511844	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15835885	TGCTCTTATTTCAAT[A/G]CCCAATTTTCTAGTT	80013
rs79543877	snp	C/G	0.0168055	0.0901129	intron-variant	FAM188A	GRCh38.p7	10:15851513	CTGCTTGATACACCT[C/G]CTAACCATTTCTCTG	80013
rs79592666	snp	A/T	0.029116	0.117091	intron-variant	FAM188A	GRCh38.p7	10:15788504	TTTCATTATGTTTGA[A/T]AAGCTCAAGTTTTTG	80013
rs79647452	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15796697	AATCAACTTCTACAT[A/G]TCCAGAATTTTAATT	80013
rs79654365	snp	C/T	0.0295035	0.117819	intron-variant	FAM188A	GRCh38.p7	10:15807289	GTGTGGGAAATCAGT[C/T]AGTGCCACAAGAAGG	80013
rs79699716	snp	C/T	0.0700422	0.173537	intron-variant	FAM188A	GRCh38.p7	10:15853934	TGTGACTCTGACAGC[C/T]TCTCAATGCTTACAG	80013
rs79713381	snp	C/T	0.0792508	0.182605	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15779646	AACCAATTTGAATGT[C/T]TGTCAACAAAACTTG	80013
rs79729545	snp	A/T	0.5	0	intron-variant	FAM188A	GRCh38.p7	10:15845675	AGCTAATTTTTTCAA[A/T]TTTTTTTTTTTTTTA	80013
rs79818927	snp	C/T	0.0766824	0.180169	intron-variant	FAM188A	GRCh38.p7	10:15790665	ATTACAGGTGGAGTC[C/T]CCCTCATCCAAAATG	80013
rs79890493	snp	C/G	0.0225045	0.103662	intron-variant	FAM188A	GRCh38.p7	10:15802424	AGGCAGCAGGGGAGA[C/G]AGCATGCAGGGGAAG	80013
rs80145816	snp	C/T	0.0158469	0.0875917	intron-variant	FAM188A	GRCh38.p7	10:15828707	TACAGCAGTTTCTTA[C/T]AGCTAAAAATGGAAA	80013
rs80154311	snp	C/T	0.0158469	0.0875917	downstream-variant-500B	FAM188A	GRCh38.p7	10:15777997	TGGGTTCTCATGCTT[C/T]TGGCTGGCTGAGTTA	80013
rs80202701	snp	C/G	0.0588605	0.161139	intron-variant	FAM188A	GRCh38.p7	10:15859494	CCTGTTACAGTGCAA[C/G]AATTCAATAAATGCT	80013
rs80206007	snp	A/G	0.0335038	0.125018	intron-variant	FAM188A	GRCh38.p7	10:15816817	ATAACTTAAAAAAAA[A/G]TCCTGCTATAAGCAT	80013
rs80230738	snp	A/G	0.0345262	0.126772	intron-variant	FAM188A	GRCh38.p7	10:15803990	GTACCCTCAGTAGGA[A/G]GAGATCCTACACATG	80013
rs80333038	snp	C/T	0.0154538	0.0865337	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15784501	TGTAATCCCAGCACT[C/T]TGGAAGGCCAGGACG	80013
rs80333123	snp	G/T	0.0193772	0.0965046	intron-variant	FAM188A	GRCh38.p7	10:15846365	AATCTAATTTACATA[G/T]GGACATAACAAGGAA	80013
rs111261686	snp	C/T	0.5	0	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15783066	CCCTCCTTAGAATTT[C/T]TTCCAACTGGAATTA	80013
rs111280365	snp	C/T	0.5	0	utr-variant-5-prime, missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15837293	CAGCATCTTTTAATT[C/T]TGGTAAACTTCTGAA	80013
rs111360573	snp	C/T	0.00199481	0.0315187	intron-variant	FAM188A	GRCh38.p7	10:15791248	GAAGACTTACTTTGA[C/T]ATGTTAACCATACCT	80013
rs111365619	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15801815	AGATATTGTGCATGA[A/G]TTCATAGGATTTACA	80013
rs111369716	snp	G/T	0.5	0	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15784866	GAAAGGGGACATCAG[G/T]GGTATGTAGGGCATG	80013
rs111377198	snp	G/T	0.00517822	0.0506191	intron-variant	FAM188A	GRCh38.p7	10:15816085	AGCCTGGCCAACATG[G/T]CGAAACTGTCTCTAC	80013
rs111418994	snp	A/G	0.0670745	0.170406	intron-variant	FAM188A	GRCh38.p7	10:15860092	TCAGCGCTGAGCACG[A/G]CGACTGGGGCAGAGA	80013
rs111419033	snp	A/G	0	0	intron-variant	FAM188A	GRCh38.p7	10:15832856	GAATCACTTCAATGG[A/G]AGCAAAAAGTGGTAA	80013
rs111482368	snp	A/C	0.00636936	0.0560724	intron-variant	FAM188A	GRCh38.p7	10:15817156	ACAATATAGATTTAA[A/C]ACAGCTGGAGATAAC	80013
rs111492471	snp	C/T	0.0337553	0.125452	intron-variant	FAM188A	GRCh38.p7	10:15795747	AATTATACAGAAATA[C/T]CCTGGAAGATCTGTT	80013
rs111528624	snp	A/T	0.00279162	0.0372561	intron-variant	FAM188A	GRCh38.p7	10:15789521	GAAACATCGGCAAAT[A/T]CTTAAAAATATTTTT	80013
rs111556207	snp	G/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15817049	ATTGTGCCCGAGCAC[G/T]TCACCCATAGAGATC	80013
rs111577328	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15821361	CCTCATTTTGCCAAA[A/G]ATAAATTCATATTCA	80013
rs111580233	snp	G/T	0.240478	0.249819	intron-variant	FAM188A	GRCh38.p7	10:15850683	ATCAATGACAATGCC[G/T]GCCCAGTACAACATG	80013
rs111629424	in-del	-/A	0.00157698	0.0280357	intron-variant	FAM188A	GRCh38.p7	10:15841641	AATGGTTTCCTCTGG[-/A]AAAAAAAAAATTCTG	80013
rs111632197	snp	A/G	0.084364	0.187256	intron-variant	FAM188A	GRCh38.p7	10:15798321	ATTATCGCTGTTTAC[A/G]TAGTAGAGGGAAGCA	80013
rs111693113	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15852791	GGCCGTTCATATCCA[C/T]AGGTTTGGCGACCAC	80013
rs111700974	snp	G/T	0.0345262	0.126772	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15784430	AGTTTTGCAACTTCA[G/T]TTATTTGTGGCTGAT	80013
rs111708594	snp	C/T	0.00279162	0.0372561	intron-variant	FAM188A	GRCh38.p7	10:15815784	TCTAAAAGCTAGGTA[C/T]TATTATGAATCCCTA	80013
rs111714696	snp	C/G	0.5	0	intron-variant	FAM188A	GRCh38.p7	10:15800308	TACGGACTGTACCTG[C/G]CACCACTCACAGTCA	80013
rs111792762	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15806431	GTATGAACAAAAAGT[A/G]AGGGCCCCCAACCAA	80013
rs111843359	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15835663	CGTTTTGAGCATAAG[A/G]AAGTTGGAGAATACT	80013
rs111941181	snp	A/G	0.040671	0.13668	intron-variant	FAM188A	GRCh38.p7	10:15838520	TTAAATAACATTTCA[A/G]TTCAGCTATGCTACG	80013
rs111992277	snp	C/T	0.0287284	0.116357	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15783153	AGAATGTAGCCACTT[C/T]AGAGACAGGGGATGG	80013
rs111998805	snp	C/T	0.00279162	0.0372561	intron-variant	FAM188A	GRCh38.p7	10:15813014	TACCTGAAATAGAAC[C/T]AGAGAAGTCTTTTTT	80013
rs112077063	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15787358	GCAGACTGCAGTTTA[A/G]TGGGTTTAAAAATGA	80013
rs112160214	snp	A/G	0.0271762	0.113356	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15779373	GGTGATTTTTAAAAA[A/G]TTCAAGATCATGTGA	80013
rs112180386	snp	C/G	0.5	0	intron-variant	FAM188A	GRCh38.p7	10:15847447	TTCAAATTTGAAAAA[C/G]TTATAAGCCAGAAAA	80013
rs112264709	snp	A/G	0.00199481	0.0315187	intron-variant	FAM188A	GRCh38.p7	10:15817082	ATGCTGAATGTAAAA[A/G]TGAGTGTTAGAAGAC	80013
rs112279331	snp	A/G	0.5	0	intron-variant	FAM188A	GRCh38.p7	10:15799516	ACATTTATTAAACAT[A/G]CCAACTTTTTGATAT	80013
rs112496373	snp	C/T	0.0402882	0.136092	intron-variant	FAM188A	GRCh38.p7	10:15833447	ATTTGAACCCAAGAT[C/T]GCCTGGCTCCAAGAT	80013
rs112567603	snp	C/T	0.0236746	0.106192	intron-variant	FAM188A	GRCh38.p7	10:15836853	AAACTCACACAGTGA[C/T]TTTTCAAAAAAAAAA	80013
rs112660127	snp	A/G	0.00914312	0.0669923	intron-variant	FAM188A	GRCh38.p7	10:15815869	ATTAAAACCAAAGTC[A/G]TCTGAGGCCAAAGCT	80013
rs112661578	snp	C/T	0	0	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15784620	CCACCATATGTAGTC[C/T]CAGCTACACAGGAGG	80013
rs112661925	snp	A/C	0.5	0	intron-variant	FAM188A	GRCh38.p7	10:15798780	GCAAGACTCTGTCTC[A/C]AAAACAAACAAACAA	80013
rs112713843	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15782552	AACATTTGCTAAAGT[A/G]TATCTCCTTTTCTAT	80013
rs112717167	snp	A/G	0.199564	0.24486	intron-variant	FAM188A	GRCh38.p7	10:15848434	GGTCAGGAGATCGAG[A/G]CCATCCTGGCTAACA	80013
rs112827439	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15806234	ATTGAGAGCAGTCTA[G/T]ATTTTCCTCTTGTGT	80013
rs112888085	snp	A/T	0.5	0	intron-variant	FAM188A	GRCh38.p7	10:15812217	AAGTGTTAGGATTAC[A/T]GGCATGAGCCCCTGC	80013
rs112979947	snp	A/G	0.5	0	intron-variant	FAM188A	GRCh38.p7	10:15799918	TAGAATATTAGTGTT[A/G]GACTGAGGTTACGGC	80013
rs112988763	in-del	-/G	0.5	0	intron-variant	FAM188A	GRCh38.p7	10:15798469	GTGCCAAGTGTTTTT[-/G]TTTTTTTTTTTAAAT	80013
rs112989066	snp	A/C	0	0	intron-variant	FAM188A	GRCh38.p7	10:15852182	TAATCATCTGCCTTG[A/C]CTGACCGGTGTTGTA	80013
rs113094475	snp	C/T	0.040671	0.13668	intron-variant	FAM188A	GRCh38.p7	10:15841849	CTGAAAAATGCAGAA[C/T]TAAACATTATGAAAG	80013
rs113106756	snp	A/G	0.0345262	0.126772	intron-variant	FAM188A	GRCh38.p7	10:15803493	TACATAAAATGGTTT[A/G]GTTAGAAGGAATGTA	80013
rs113122013	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15845369	CTTACACAGTATCAT[A/G]ATCTAATTTTTATAC	80013
rs113159478	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15795431	TCTACAAGGACTTCA[C/T]GGATACAGCAACTTC	80013
rs113267010	snp	A/C/T	0.0703205	0.176502	intron-variant	FAM188A	GRCh38.p7	10:15825931	CTCTTCTATCCCTAT[A/C/T]CCATAAAGAAAATTA	80013
rs113313794	snp	A/C	0.5	0	intron-variant	FAM188A	GRCh38.p7	10:15798781	CAAGACTCTGTCTCA[A/C]AAACAAACAAACAAA	80013
rs113318067	snp	A/T	0.0718919	0.175435	intron-variant	FAM188A	GRCh38.p7	10:15826881	CCATTCATAAATACA[A/T]AATCCAGATAGACTA	80013
rs113369420	snp	A/G	0.5	0	intron-variant	FAM188A	GRCh38.p7	10:15842577	ATAGTCATGGTTTGG[A/G]ATGTAAGCTGTTACA	80013
rs113423431	snp	A/C	0.5	0	intron-variant	FAM188A	GRCh38.p7	10:15812220	TGTTAGGATTACAGG[A/C]ATGAGCCCCTGCGCC	80013
rs113477762	snp	C/T	0.5	0	intron-variant	FAM188A	GRCh38.p7	10:15832280	GCACCTCAACCCAAG[C/T]TCAGCAAGAACCTAT	80013
rs113526994	snp	G/T	0.5	0	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15782491	TATTTTTTTTTTAAT[G/T]ATGTGCATGTATCAC	80013
rs113567545	snp	C/T	0.5	0	intron-variant	FAM188A	GRCh38.p7	10:15851961	CAGAGACTTTACCTG[C/T]AGCCTCAATGCTCAC	80013
rs113589609	in-del	-/A	0.5	0	intron-variant	FAM188A	GRCh38.p7	10:15792107	AGTTTCTTGGGAATT[-/A]AAAAAAAAAATAGAA	80013
rs113634978	snp	C/T	0.00676609	0.0577691	intron-variant	FAM188A	GRCh38.p7	10:15817193	GCCCTAAGAGTCATT[C/T]TCAGGTTTTGCTAAA	80013
rs113653394	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15837376	TAACTACATTCATAA[A/G]AGGGAAAATTTTTAA	80013
rs113705348	snp	C/T	0.00676609	0.0577691	intron-variant	FAM188A	GRCh38.p7	10:15824095	TGCAATTAGCATGCA[C/T]GTGCAGGTATCCCTT	80013
rs113724351	snp	C/G	0.0667028	0.170006	intron-variant	FAM188A	GRCh38.p7	10:15860085	TCCAGCTTCAGCGCT[C/G]AGCACGGCGACTGGG	80013
rs113833515	snp	A/T	0.5	0	intron-variant	FAM188A	GRCh38.p7	10:15789703	CAATTAAAATAATTC[A/T]TTACCAACAAATTCC	80013
rs113852609	snp	A/C	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15848059	CAGCAAAATATCTTC[A/C]AATCATGAGGTGTGG	80013
rs113896772	snp	C/T	0	0	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15784004	TTTCTGAATCAGCTA[C/T]TAAAATACCTAGTGT	80013
rs113918458	snp	A/C	0.5	0	intron-variant	FAM188A	GRCh38.p7	10:15821484	AGCATAATCAGCTGG[A/C]TTAACCACACTTAAT	80013
rs113955738	snp	C/T	0.5	0	intron-variant	FAM188A	GRCh38.p7	10:15835282	AAGACCTACTTATTG[C/T]AACCTCATCAATTCC	80013
rs114031591	snp	C/T	0.040671	0.13668	intron-variant	FAM188A	GRCh38.p7	10:15835093	CATAAAATGGAAGGT[C/T]TACTTCTGATTGTAC	80013
rs114035593	snp	C/T	0.0119996	0.0765233	intron-variant	FAM188A	GRCh38.p7	10:15816960	TAAACAAATTAAAAA[C/T]TTATACTGCCTCTTA	80013
rs114041185	snp	A/C	0.0618563	0.164627	intron-variant	FAM188A	GRCh38.p7	10:15858115	AACAGTTAACATATC[A/C]AAACCAGTAACAGGA	80013
rs114051893	snp	C/G	0.0111196	0.0737302	intron-variant	FAM188A	GRCh38.p7	10:15812414	AATTCAATACAGCTT[C/G]TGATATTTTACTCTA	80013
rs114051998	snp	C/G	0.00597247	0.0543191	intron-variant	FAM188A	GRCh38.p7	10:15801453	GAAGTTACCTAGTAC[C/G]CTGCCAGTAAGAGAC	80013
rs114062461	snp	A/G	0.0452528	0.143452	intron-variant	FAM188A	GRCh38.p7	10:15787703	GACCTCCTACCTGAC[A/G]TCTAGTATTGGCCCT	80013
rs114071477	snp	C/T	0.0115144	0.0749975	intron-variant	FAM188A	GRCh38.p7	10:15805967	CATTGCTTTTAGAGA[C/T]GTTAAAACATTCTCA	80013
rs114078232	snp	C/T	0.0383715	0.133092	intron-variant	FAM188A	GRCh38.p7	10:15844759	CAAATTTGTACTATA[C/T]AGCAGTATATGAGTG	80013
rs114104853	snp	A/G	0.00676609	0.0577691	intron-variant	FAM188A	GRCh38.p7	10:15820357	TGCAAAGACCACCAG[A/G]GTCTTAAGGGATACA	80013
rs114116722	snp	A/G	0.046775	0.145601	intron-variant	FAM188A	GRCh38.p7	10:15850354	GGGAACAAGGGAGAT[A/G]ATCATTAGGTCTGAC	80013
rs114224008	snp	A/G	0.0402882	0.136092	intron-variant	FAM188A	GRCh38.p7	10:15839654	TATAAAACACAAGAA[A/G]AAGAACAAAGCTGGG	80013
rs114241414	snp	A/T	0.0023933	0.0345097	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15784100	ATCAGCTACTAAGAT[A/T]CCTAGTGTATGACCT	80013
rs114253884	snp	A/G	0.0402882	0.136092	intron-variant	FAM188A	GRCh38.p7	10:15828827	GCATTTACTGGACTT[A/G]TTTCCTGCTCTGACA	80013
rs114255925	snp	A/G	0.0379877	0.132479	intron-variant	FAM188A	GRCh38.p7	10:15807366	CAGCGGACACAATAC[A/G]AATGGTGGAAGGTTG	80013
rs114281110	snp	A/T	0.0193772	0.0965046	intron-variant	FAM188A	GRCh38.p7	10:15836546	TTTCAGACATGATAG[A/T]TCTAATAGCATAGTC	80013
rs114366440	snp	G/T	0.0463947	0.145069	intron-variant	FAM188A	GRCh38.p7	10:15851376	CCTGTATTATCTGGC[G/T]CCTGCCTGCATCTCC	80013
rs114368891	snp	A/C	0.040671	0.13668	intron-variant	FAM188A	GRCh38.p7	10:15831625	CTAATATATTCTGTA[A/C]AGGAAGTAACGACTT	80013
rs114372412	snp	C/T	0.040671	0.13668	intron-variant	FAM188A	GRCh38.p7	10:15832310	TTGCTTCCCTAATCA[C/T]ATGAGATAAGATACC	80013
rs114385406	snp	A/G	0.0387552	0.1337	intron-variant	FAM188A	GRCh38.p7	10:15813738	CACACAAAGAATTCC[A/G]CTGTTCTTCACAGGC	80013
rs114434750	snp	A/C	0.0372196	0.131242	intron-variant	FAM188A	GRCh38.p7	10:15803702	GTGCACTTAAGGTCG[A/C]AGTCTAATAGAACAG	80013
rs114441862	snp	A/G	0.0402882	0.136092	intron-variant	FAM188A	GRCh38.p7	10:15827952	TACACACTTCAAAGA[A/G]TAAGTTTATACTTTT	80013
rs114446998	snp	C/T	0.0337553	0.125452	intron-variant	FAM188A	GRCh38.p7	10:15817714	TAGCAATACAATTTG[C/T]TGCATTTTCCTTTTT	80013
rs114459736	snp	C/T	0.0248432	0.108648	intron-variant	FAM188A	GRCh38.p7	10:15822296	AGGCTATGACTTTAC[C/T]AAAGACGACAGATGA	80013
rs114555567	snp	A/T	0.0471551	0.14613	intron-variant	FAM188A	GRCh38.p7	10:15836342	TATGCCCTTGATTCC[A/T]TCTAATAGGTTCAGA	80013
rs114558416	snp	A/G	0.0383715	0.133092	intron-variant	FAM188A	GRCh38.p7	10:15818613	CCAACTGATGAACAG[A/G]TAAAATTGGTTTAAC	80013
rs114567344	snp	A/G	0.0437281	0.141251	intron-variant	FAM188A	GRCh38.p7	10:15798072	TTATTCTTTCTATTC[A/G]CCATCTGTTACATTC	80013
rs114592272	snp	C/T	0.00636936	0.0560724	intron-variant	FAM188A	GRCh38.p7	10:15788426	GAACTCATCTAAAAA[C/T]GGAACAAGACCAAAT	80013
rs114604854	snp	C/T	0.0364509	0.129988	intron-variant	FAM188A	GRCh38.p7	10:15787235	TATACTGTATTGGTC[C/T]AGCAGCAGCCTAAAG	80013
rs114608129	snp	C/T	0.0788843	0.182262	intron-variant	FAM188A	GRCh38.p7	10:15810033	TTTTTAATGATGATT[C/T]TCAAGTAAAACTGAC	80013
rs114700410	snp	C/T	0.030665	0.119967	intron-variant	FAM188A	GRCh38.p7	10:15838999	GGCACACAGAAAAAT[C/T]CTCTCAAGAGTACAT	80013
rs114715319	snp	A/G	0.0123036	0.0774623	intron-variant	FAM188A	GRCh38.p7	10:15834103	AAAAGAAGGACTCAC[A/G]TATTAGAGTAGGTTA	80013
rs114800746	snp	A/G	0.0368353	0.130617	intron-variant	FAM188A	GRCh38.p7	10:15797887	CTAGTATAAGCTTTA[A/G]CTCCCTTAACTATTT	80013
rs114801155	snp	C/T	0.040671	0.13668	intron-variant	FAM188A	GRCh38.p7	10:15825134	CTGAAATCCGAAATG[C/T]TCCAAGATCTGAAGC	80013
rs114805642	snp	C/T	0.0345262	0.126772	intron-variant	FAM188A	GRCh38.p7	10:15829151	TGAGGTAAAGCACCA[C/T]AGATGATCAGAGGGA	80013
rs114871668	snp	C/T	0.0383715	0.133092	intron-variant	FAM188A	GRCh38.p7	10:15819706	CTCCCTCATTTGCAG[C/T]TGGAAGGAACAGAGT	80013
rs114898430	snp	C/T	0.040671	0.13668	intron-variant	FAM188A	GRCh38.p7	10:15825662	CCTAACTATAATATC[C/T]GTTTCTGTTTATTTT	80013
rs114906792	snp	A/G	0.0322114	0.122752	intron-variant	FAM188A	GRCh38.p7	10:15832804	GTTAATTAACTACAC[A/G]TTTCTGAATTTGAGA	80013
rs114931942	snp	A/C	0.0379877	0.132479	intron-variant	FAM188A	GRCh38.p7	10:15844791	GCCAGCATCTTCCCA[A/C]CCTTACATGCACTGG	80013
rs114936630	snp	C/G	0.0376037	0.131863	intron-variant	FAM188A	GRCh38.p7	10:15794381	TAATCTACTTTTAAT[C/G]CTTCTTAGAGCTGAC	80013
rs114941459	snp	A/G	0.0383715	0.133092	intron-variant	FAM188A	GRCh38.p7	10:15823474	AAGCCAAGCATTAAA[A/G]GGATTTGCAAAAATT	80013
rs114954861	snp	A/C	0.00676609	0.0577691	intron-variant	FAM188A	GRCh38.p7	10:15843390	ATCTTTTGACTAGTT[A/C]TGTAAAGATGTCAAA	80013
rs114958536	snp	A/C	0.0383715	0.133092	intron-variant	FAM188A	GRCh38.p7	10:15824417	TAAAGTGAATTAATA[A/C]GTATTTAAAAATTTC	80013
rs114990664	snp	A/T	0.00914312	0.0669923	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15783846	ATTATTTGAACTTAA[A/T]TAACCATTTTCCTGT	80013
rs115023577	snp	A/C	0.0383715	0.133092	intron-variant	FAM188A	GRCh38.p7	10:15835677	GAAAGTTGGAGAATA[A/C]TGAACAGTCAAGAAG	80013
rs115072884	snp	C/T	0.039522	0.134904	intron-variant	FAM188A	GRCh38.p7	10:15816945	GCAAAATAAAACAAA[C/T]AAACAAATTAAAAAT	80013
rs115081480	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15854719	AGGGCTCAGCTAAGA[C/T]TTAACTACATTTGTA	80013
rs115085175	snp	A/G	0.0376037	0.131863	intron-variant	FAM188A	GRCh38.p7	10:15791866	AGGATTTCTGTCCTG[A/G]AAGATTAAGAAATAA	80013
rs115145893	snp	C/T	0.040671	0.13668	intron-variant	FAM188A	GRCh38.p7	10:15837853	TAACAAAAATATCGG[C/T]ATTCTTAATAAAAGG	80013
rs115147775	snp	A/G	0.0399052	0.1355	intron-variant	FAM188A	GRCh38.p7	10:15820280	TGGAGAGGGCTCGGC[A/G]TGTCTGGGAAAGTGA	80013
rs115152951	snp	A/C	0.0383715	0.133092	intron-variant	FAM188A	GRCh38.p7	10:15791187	TAATTCAAAACTTTT[A/C]ATATACTCAAGATTA	80013
rs115163680	snp	C/G	0.0588605	0.161139	intron-variant	FAM188A	GRCh38.p7	10:15859661	AAACGGGGATACTTT[C/G]GGCCAAGAGTACACT	80013
rs115166455	snp	A/T	0.040671	0.13668	intron-variant	FAM188A	GRCh38.p7	10:15841339	ATGTTATGAAAATTT[A/T]AAGTAATTTTTTCTT	80013
rs115190644	snp	A/G	0.0383715	0.133092	intron-variant	FAM188A	GRCh38.p7	10:15821166	TGCATGTGTCAAAGA[A/G]TTTAATGTTGTAAAA	80013
rs115266136	snp	C/T	0.0387552	0.1337	intron-variant	FAM188A	GRCh38.p7	10:15814399	CTTAGGGGATATAAA[C/T]GTCACTGGAACCCAA	80013
rs115295768	snp	C/T	0.046775	0.145601	intron-variant	FAM188A	GRCh38.p7	10:15850017	GCTGTGACAGAAGAA[C/T]ATAAATCGTGAAGAT	80013
rs115297311	snp	A/G	0.0383715	0.133092	intron-variant	FAM188A	GRCh38.p7	10:15810767	CTTACTACAGAGAGA[A/G]ACAGATAATATAGAA	80013
rs115312086	snp	A/G	0.0314385	0.121371	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15784058	GTTCTCTAATCTTCA[A/G]TTTCCTCATTGTCAA	80013
rs115321521	snp	C/T	0.079617	0.182947	intron-variant	FAM188A	GRCh38.p7	10:15807403	GAATGCTGAGCAAGA[C/T]TTTGATAAGCGTATT	80013
rs115333932	snp	A/G	0.00835141	0.0640778	intron-variant	FAM188A	GRCh38.p7	10:15802750	ACTGGTTAGGCTCCA[A/G]ATAACAAAACCACCA	80013
rs115362124	snp	G/T	0.039522	0.134904	intron-variant	FAM188A	GRCh38.p7	10:15812604	TACGTGGTGCATCAG[G/T]CTACATAACAGATTG	80013
rs115371371	snp	G/T	0.046775	0.145601	intron-variant	FAM188A	GRCh38.p7	10:15850974	CGTTGAAATATTGGG[G/T]GCTGGTTCCCCCGAT	80013
rs115372518	snp	A/G	0.00597247	0.0543191	intron-variant	FAM188A	GRCh38.p7	10:15831547	TGACAGCCTTGAAAA[A/G]CACTATTTCAAGGAA	80013
rs115373370	snp	A/G	0.0452528	0.143452	intron-variant	FAM188A	GRCh38.p7	10:15852801	ATCCATAGGTTTGGC[A/G]ACCACAGATTCAACC	80013
rs115435712	snp	A/G	0.00318978	0.0398085	intron-variant	FAM188A	GRCh38.p7	10:15857551	TGCTATTCTTTAAAA[A/G]GTACTATAGGCAATT	80013
rs115437651	snp	C/T	0.00874735	0.0655527	intron-variant	FAM188A	GRCh38.p7	10:15836931	GGGTCAAGTGCTACA[C/T]GGAAGGATCAAAGGA	80013
rs115457831	snp	G/T	0.0383715	0.133092	intron-variant	FAM188A	GRCh38.p7	10:15818856	CATGGGACTGCTAAT[G/T]GGTTTAGAGCTCCTT	80013
rs115474442	snp	A/G	0.00597247	0.0543191	intron-variant	FAM188A	GRCh38.p7	10:15856737	AGCAATCAATATTGA[A/G]AAGAAAATAAATTCC	80013
rs115500098	snp	A/G	0.0696718	0.173152	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15862121	TTGTATTTGCAAAGA[A/G]TTATTTGCTTTTCTC	80013
rs115501554	snp	C/T	0.00636936	0.0560724	intron-variant	FAM188A	GRCh38.p7	10:15842937	AAAGACTGTTCTTTA[C/T]GGCATGCTGCCACCT	80013
rs115508021	snp	C/T	0.00676609	0.0577691	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15861985	CAAATCTTACCTATC[C/T]TTCATGTCAGAGTGT	80013
rs115512095	snp	C/T	0.0402882	0.136092	intron-variant	FAM188A	GRCh38.p7	10:15829433	GGCCTTGGCATATGA[C/T]TTTAAATTTCTCCTA	80013
rs115517939	snp	A/C	0.00676609	0.0577691	intron-variant	FAM188A	GRCh38.p7	10:15843394	TTTGACTAGTTCTGT[A/C]AAGATGTCAAATGGG	80013
rs115538673	snp	C/T	0.0463947	0.145069	intron-variant	FAM188A	GRCh38.p7	10:15813223	TGCTATTCTTCCAGC[C/T]TCATCTTACACCTTG	80013
rs115538776	snp	A/G	0.0325976	0.123435	intron-variant	FAM188A	GRCh38.p7	10:15856979	CCTCAAACACAGCAG[A/G]CAGATCAGTCCTTTA	80013
rs115546808	snp	C/T	0.0463947	0.145069	intron-variant	FAM188A	GRCh38.p7	10:15851678	GACCTTAAATACTGT[C/T]GAGTTTCCAACCACG	80013
rs115670469	snp	C/T	0.0379877	0.132479	intron-variant	FAM188A	GRCh38.p7	10:15844269	AATATGCTAATCAAG[C/T]GCTTCTGATTTTTCC	80013
rs115695555	snp	C/T	0.0391387	0.134304	intron-variant	FAM188A	GRCh38.p7	10:15831246	GATTAATTTAGAGTA[C/T]GCCCAACCAATGAAA	80013
rs115715623	snp	C/T	0.00398564	0.0444627	intron-variant	FAM188A	GRCh38.p7	10:15781933	GGGGGTGTATTTAGT[C/T]ATGGTGAAACTACTG	80013
rs115724133	snp	A/G	0.0298908	0.118541	intron-variant	FAM188A	GRCh38.p7	10:15787457	TACTACACAACATGC[A/G]AAGTGTTGTGTTTGG	80013
rs115726270	snp	C/T	0.0298908	0.118541	intron-variant	FAM188A	GRCh38.p7	10:15810446	TTCTATTCAATAATA[C/T]GGGTGGTTTGAATTG	80013
rs115730979	snp	A/G	0.040671	0.13668	intron-variant	FAM188A	GRCh38.p7	10:15829784	AAAGGAAGAAAAAAG[A/G]GAGCAGCTAGCATTT	80013
rs115732673	snp	A/G	0.0402882	0.136092	intron-variant	FAM188A	GRCh38.p7	10:15832943	AGCTTCGTGTCCTAT[A/G]CTACGTACTTCAGAG	80013
rs115741881	snp	C/T	0.0383715	0.133092	intron-variant	FAM188A	GRCh38.p7	10:15848733	TTAATTTAAATATTA[C/T]CCAACCAGCATTGAC	80013
rs115797245	snp	A/G	0.0696718	0.173152	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15861508	AAAGTAACACATACA[A/G]AGGATTTGGTGTACT	80013
rs115800378	snp	C/T	0.0111196	0.0737302	intron-variant	FAM188A	GRCh38.p7	10:15822955	TGGGTAAAAATTATG[C/T]TCACTGTAAACATAA	80013
rs115850298	snp	C/T	0.00676609	0.0577691	intron-variant	FAM188A	GRCh38.p7	10:15819204	ACACTTATCAAAGCA[C/T]GGGGAAATGTTCAGA	80013
rs115858021	snp	G/T	0.0174175	0.0916809	intron-variant	FAM188A	GRCh38.p7	10:15813042	TTTACCTATTCCCTG[G/T]GTTATCCTTCAATAT	80013
rs115861857	snp	C/T	0.00636936	0.0560724	intron-variant	FAM188A	GRCh38.p7	10:15836495	CATAGAGTCAATCAA[C/T]GCTCAAAAAACATTT	80013
rs115864354	snp	C/G/T	0.041867	0.13875	intron-variant	FAM188A	GRCh38.p7	10:15835162	AAATGCAAATTAGGA[C/G/T]GGCAGGAAGTGCCTT	80013
rs115870502	snp	A/C	0.0379877	0.132479	intron-variant	FAM188A	GRCh38.p7	10:15802081	TATAAAATACAAAAT[A/C]TGTGTTAATCTACTG	80013
rs115917813	snp	A/C	0.0383715	0.133092	intron-variant	FAM188A	GRCh38.p7	10:15827168	ACATAAAATTGATAT[A/C]ACAGGAGTAAAAAAA	80013
rs115919079	snp	C/T	0.0509478	0.151255	intron-variant	FAM188A	GRCh38.p7	10:15794714	ATTTTCCTTGGTACA[C/T]TGTAAAAGAAAATAA	80013
rs115928094	snp	C/T	0.0383715	0.133092	intron-variant	FAM188A	GRCh38.p7	10:15836263	CCTCCAGCTTTCCCA[C/T]ATAGAAAACTTGCCC	80013
rs115971764	snp	A/G	0.0402882	0.136092	intron-variant	FAM188A	GRCh38.p7	10:15829340	CTTAACCCTGACTAC[A/G]CAATATCACTTGCTT	80013
rs115978362	snp	A/C	0.00199481	0.0315187	intron-variant	FAM188A	GRCh38.p7	10:15832688	TGAACTTAGTTCTTA[A/C]ATTTTTTAAACAGTA	80013
rs115984538	snp	C/T	0.00795532	0.062565	intron-variant	FAM188A	GRCh38.p7	10:15790541	TGATTTTGCTTAAGT[C/T]AAGTCATAGCTAAAG	80013
rs115985321	snp	A/G	0.0345262	0.126772	intron-variant	FAM188A	GRCh38.p7	10:15814407	ATATAAACGTCACTG[A/G]AACCCAAATGCGGGA	80013
rs116034842	snp	G/T	0.0383715	0.133092	intron-variant	FAM188A	GRCh38.p7	10:15809242	ACTTAAATAATTATG[G/T]ATTATTATGAAAGAC	80013
rs116041656	snp	A/C	0.0107246	0.0724382	intron-variant	FAM188A	GRCh38.p7	10:15789604	AGTGTTACAGCGTTA[A/C]GTGGGTAAAATATTT	80013
rs116052275	snp	G/T	0.040671	0.13668	intron-variant	FAM188A	GRCh38.p7	10:15830109	AGCTTGTTGAATAAA[G/T]TAACATCAGAAAACA	80013
rs116054555	snp	A/G	0.0298908	0.118541	intron-variant	FAM188A	GRCh38.p7	10:15836826	TAAGAATCGTGAGAC[A/G]TTATAGAAAGAAAAC	80013
rs116058324	snp	A/C	0.0444908	0.142359	intron-variant	FAM188A	GRCh38.p7	10:15787459	CTACACAACATGCAA[A/C]GTGTTGTGTTTGGGG	80013
rs116063761	snp	A/C	0.0341408	0.126114	intron-variant	FAM188A	GRCh38.p7	10:15810573	AAGCACACCTCCCGA[A/C]CCCCAACTTATCAAG	80013
rs116065123	snp	C/T	0.0383715	0.133092	intron-variant	FAM188A	GRCh38.p7	10:15849298	TCAGAGAAAATTTAA[C/T]ACAGCTAAAGGGTAG	80013
rs116097755	snp	C/T	0.00478085	0.0486577	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15784315	TTCTTCCTGCATCAG[C/T]CTCTACATCATAGCA	80013
rs116141552	snp	A/C/G	0.0189964	0.095673	intron-variant	FAM188A	GRCh38.p7	10:15810760	CACAGAGCTTACTAC[A/C/G]GAGAGAGACAGATAA	80013
rs116146754	snp	A/G	0.0463947	0.145069	intron-variant	FAM188A	GRCh38.p7	10:15849751	CTCTCTTTATCTTCA[A/G]TCTCTTCCAGGAAGC	80013
rs116154361	snp	A/T	0.0383715	0.133092	intron-variant	FAM188A	GRCh38.p7	10:15835394	TAAGAATTAAATAGA[A/T]GATTAATTAACAACC	80013
rs116179164	snp	A/G	0.00993419	0.0697739	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15783039	ATCCGATGGATACAA[A/G]CAGGCACATGGCCCT	80013
rs116181065	snp	C/T	0.0217236	0.101931	intron-variant	FAM188A	GRCh38.p7	10:15827241	GACCAAATGATTTAA[C/T]CTCATAAATATGAAA	80013
rs116208541	snp	C/T	0.0667028	0.170006	intron-variant	FAM188A	GRCh38.p7	10:15858806	TACAATGGAAGTAAA[C/T]TTTTTCTTAGTCTTT	80013
rs116237336	snp	C/T	0.00676609	0.0577691	intron-variant	FAM188A	GRCh38.p7	10:15851548	ACTCAAACTTACCTA[C/T]AGGTTTCACCCTAAG	80013
rs116237679	snp	G/T	0.0387552	0.1337	intron-variant	FAM188A	GRCh38.p7	10:15819230	TCAGACTTACAAAAT[G/T]AACACAAGCTCAATG	80013
rs116299588	snp	A/G	0.040671	0.13668	intron-variant	FAM188A	GRCh38.p7	10:15829343	AACCCTGACTACACA[A/G]TATCACTTGCTTAAA	80013
rs116310848	snp	A/C	0.0700422	0.173537	intron-variant	FAM188A	GRCh38.p7	10:15853825	TCTGGCTGACATTTT[A/C]TCAAAAATAAGTGAG	80013
rs116311319	snp	C/T	0.00676609	0.0577691	intron-variant	FAM188A	GRCh38.p7	10:15820530	GGGGAAGGGGACACA[C/T]TTTGATTCTCTAGTT	80013
rs116312165	snp	A/G	0.0376037	0.131863	intron-variant	FAM188A	GRCh38.p7	10:15848357	TACATGGCATTGGCC[A/G]GGCACAGTGGCTCAC	80013
rs116314887	snp	A/G	0.0700422	0.173537	intron-variant	FAM188A	GRCh38.p7	10:15858164	GATAACTTCAAAAAT[A/G]TATGTTTGGTTGCCT	80013
rs116334752	snp	A/C	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15804088	ATTGTAAAAGCAGTT[A/C]TTTACATTAGTCTGA	80013
rs116405299	snp	G/T	0.0383715	0.133092	intron-variant	FAM188A	GRCh38.p7	10:15817848	CTGGCCCTGTGGAAT[G/T]TATTCTTATCACTAG	80013
rs116406239	snp	A/T	0.030278	0.119257	intron-variant	FAM188A	GRCh38.p7	10:15855814	TGAGGATAACTACAT[A/T]TGTTCTTTCCTATCT	80013
rs116451212	snp	A/G	0.00755907	0.0610114	intron-variant	FAM188A	GRCh38.p7	10:15839886	CTAAAATGTTTTCTG[A/G]AGGGTAATTCAATAT	80013
rs116451557	snp	A/T	0.0463947	0.145069	intron-variant	FAM188A	GRCh38.p7	10:15812954	AAATCCATGCACTTT[A/T]TTCCTCTCTACCTCA	80013
rs116482840	snp	G/T	0.040671	0.13668	intron-variant	FAM188A	GRCh38.p7	10:15835123	CTTTCTCACAAATGT[G/T]GGTCATTCAAATGTA	80013
rs116483010	snp	A/C	0.0221141	0.102801	intron-variant	FAM188A	GRCh38.p7	10:15787770	GTATAGTATACTGTA[A/C]AAAGGATATGGCATT	80013
rs116483970	snp	A/G	0.0402882	0.136092	intron-variant	FAM188A	GRCh38.p7	10:15830912	ATTTTTGTTTTAGGC[A/G]GTAGAAGCCACCTAA	80013
rs116489986	snp	A/G	0.0399052	0.1355	intron-variant	FAM188A	GRCh38.p7	10:15822735	ATACAGGAGAGAAAC[A/G]TCAGGGTTGGAGATA	80013
rs116551833	snp	C/G	0.0383715	0.133092	intron-variant	FAM188A	GRCh38.p7	10:15832179	ACCAAGTGTGAGAGA[C/G]AGTGATGCGCTAAAG	80013
rs116554091	snp	C/T	0.0376037	0.131863	intron-variant	FAM188A	GRCh38.p7	10:15788986	TTTGCAGAGAAACTT[C/T]TTAAAGTTTATAGAA	80013
rs116555957	snp	A/G	0.0345262	0.126772	intron-variant	FAM188A	GRCh38.p7	10:15836810	AGAAAACAAAACAAA[A/G]TAAGAATCGTGAGAC	80013
rs116581246	snp	C/T	0.0170251	0.090679	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15780289	AGTGCTAAAGATACA[C/T]TGTAACGTGAAATAC	80013
rs116608402	snp	G/T	0.0402882	0.136092	intron-variant	FAM188A	GRCh38.p7	10:15825466	CCTCCCGCTTTGGCC[G/T]CCCAAACTGCTGAGA	80013
rs116610819	snp	C/G	0.00597247	0.0543191	intron-variant	FAM188A	GRCh38.p7	10:15787667	TCTCTCCCGGAAACA[C/G]CTGGGTCAGGCTGCC	80013
rs116637212	snp	C/T	0.0456336	0.143994	intron-variant	FAM188A	GRCh38.p7	10:15811301	TTAGCCAATATACTA[C/T]ACTACTTTCATCATA	80013
rs116639199	snp	C/T	0.030278	0.119257	intron-variant	FAM188A	GRCh38.p7	10:15853651	CCCATAAAGCACTTA[C/T]GCTACATACTGGGTA	80013
rs116639623	snp	C/T	0.00636936	0.0560724	intron-variant	FAM188A	GRCh38.p7	10:15814949	GTGAAATCTCTCCTA[C/T]TGTTCTGACAACAAA	80013
rs116646426	snp	C/T	0.0410537	0.137264	intron-variant	FAM188A	GRCh38.p7	10:15839159	GGTGAGTTAAGAAAA[C/T]TGATTCATTATGAAG	80013
rs116675836	snp	C/T	0.0402882	0.136092	intron-variant	FAM188A	GRCh38.p7	10:15842209	TCTTTTCAAGCAGTA[C/T]TACTCTCAAGAAGTA	80013
rs116702608	snp	C/T	0.040671	0.13668	intron-variant	FAM188A	GRCh38.p7	10:15832116	GGGACTAGGGTAAGC[C/T]ATCGAGAATCCGGAG	80013
rs116703990	snp	A/G	0.0402882	0.136092	intron-variant	FAM188A	GRCh38.p7	10:15827624	AAGTTAACAAGAAAG[A/G]GAAGGCTGGGTGACA	80013
rs116710852	snp	A/G	0.0402882	0.136092	intron-variant	FAM188A	GRCh38.p7	10:15817461	GTTCAAAGTTTCACA[A/G]TATGAACAGTCTCTT	80013
rs116712359	snp	C/T	0.00636936	0.0560724	intron-variant	FAM188A	GRCh38.p7	10:15855486	TTACGTCTGAAATTA[C/T]CCATCTTAAAACACC	80013
rs116737913	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15823424	GTATCAGACTAAATT[C/T]ATAAGCATATATGAA	80013
rs116765732	snp	C/T	0.0788843	0.182262	intron-variant	FAM188A	GRCh38.p7	10:15808087	TAATAATTCAAATCA[C/T]TGAGAATAATTAAGC	80013
rs116776019	snp	C/T	0.00398564	0.0444627	intron-variant	FAM188A	GRCh38.p7	10:15833079	CCTTAACGGAATGGA[C/T]TGGCCAAAATGGGAT	80013
rs116791339	snp	C/G	0.0517044	0.152246	intron-variant	FAM188A	GRCh38.p7	10:15790948	CAGTTCCCACCCCAA[C/G]CAAGAGCTAATTGGC	80013
rs116793946	snp	A/G	0.0379877	0.132479	intron-variant	FAM188A	GRCh38.p7	10:15829498	GTGGATTAAAGCACT[A/G]GATTTGTGAAGGAGA	80013
rs116798831	snp	A/G	0.0383715	0.133092	intron-variant	FAM188A	GRCh38.p7	10:15819476	CTCCCACACTCCAGG[A/G]ATCACCCTAATCACC	80013
rs116802587	snp	C/T	0.0325976	0.123435	intron-variant	FAM188A	GRCh38.p7	10:15856980	CTCAAACACAGCAGG[C/T]AGATCAGTCCTTTAA	80013
rs116802996	snp	C/T	0.00636936	0.0560724	intron-variant	FAM188A	GRCh38.p7	10:15824782	TGTCTAATAATAATA[C/T]CATGTTACTAAATAC	80013
rs116844244	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15810962	GCTCATTAGTCATTA[A/G]GGAAATGCAAATCAA	80013
rs116957342	snp	A/C/T	0.0107246	0.0724382	intron-variant	FAM188A	GRCh38.p7	10:15800702	GCTTGATATGCACCA[A/C/T]GGATTGAGGTCTGCT	80013
rs116976424	snp	C/T	0.0327778	0.123752	intron-variant	FAM188A	GRCh38.p7	10:15802044	CTTTTCTCCGGCTTA[C/T]GAGATTACAGTATAT	80013
rs117003955	snp	C/T	0.00835141	0.0640778	intron-variant	FAM188A	GRCh38.p7	10:15859068	GCAACTTTGGCCCAG[C/T]CATTTACCTTTACAA	80013
rs117028015	snp	C/T	0.0182669	0.0938071	utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant	FAM188A	GRCh38.p7	10:15778831	CATAAAGCTTTAGGA[C/T]AAATAATTTAAACAT	80013
rs117094573	snp	C/T	0.0325976	0.123435	intron-variant	FAM188A	GRCh38.p7	10:15822702	AGAGGGATAAATAGC[C/T]GGAAGTAAGGCTCAG	80013
rs117125833	snp	A/G	0.00914312	0.0669923	intron-variant	FAM188A	GRCh38.p7	10:15842499	TTTTGTATTTCACCT[A/G]TTAATTTAAAACTTA	80013
rs117185689	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15854089	ATACTGTTATAAATT[A/G]ATGCAGAGGTAAGAG	80013
rs117270767	snp	A/C	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15798526	GTCACGCCTGTAATC[A/C]CAGGACTTTGGGAGG	80013
rs117306912	snp	C/T	0.00835141	0.0640778	intron-variant	FAM188A	GRCh38.p7	10:15850236	ATGTCGCCTCAGGAT[C/T]CTGTGATGATTGTGT	80013
rs117386416	snp	A/G	0.0103295	0.0711199	intron-variant	FAM188A	GRCh38.p7	10:15831595	TACATCTCAAGAACC[A/G]AAACTGATAATTGAC	80013
rs117462331	snp	A/T	0.0341408	0.126114	intron-variant	FAM188A	GRCh38.p7	10:15842515	TTAATTTAAAACTTA[A/T]GGAAGTGATCCCTTA	80013
rs117476403	snp	C/T	0.0115144	0.0749975	intron-variant	FAM188A	GRCh38.p7	10:15825682	CTGTTTATTTTATAA[C/T]TGACAAATTAAAGTT	80013
rs117594299	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15853094	CTCGAACACCAACAG[A/C]CAACTATATTTAAGT	80013
rs117671511	snp	C/T	1.67144e-05	0.00289084	intron-variant, missense, utr-variant-5-prime, nc-transcript-variant	FAM188A	GRCh38.p7	10:15838246	ATTAATGCATGAAAT[C/T]GCTCAAAGCCAAGCT	80013
rs117781858	snp	C/T	0.0193772	0.0965046	intron-variant	FAM188A	GRCh38.p7	10:15805181	CAAATCCGTCAAGCT[C/T]TTCTTGAAGTTAGAC	80013
rs117807714	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15790859	CTCAGTCTGTACACC[A/G]TTTTTCAGGAGCACT	80013
rs117983477	snp	A/G	0.0138799	0.0821421	intron-variant	FAM188A	GRCh38.p7	10:15857490	GTAGTTTGTGGGAAG[A/G]GGGGAGGATAAATAG	80013
rs118091971	snp	A/G	0.0329836	0.124112	intron-variant	FAM188A	GRCh38.p7	10:15792334	GACTCATAGCTGCTC[A/G]TTAACATTTGTTACT	80013
rs137856571	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15847676	GTCAAAAGGCTACTA[C/T]TGCACAACTCATCGA	80013
rs137930085	snp	C/T	0.00676609	0.0577691	intron-variant	FAM188A	GRCh38.p7	10:15836636	CTAGAAGGGGACATA[C/T]TGGAACTATTAAATA	80013
rs137948035	snp	C/T	0.00993419	0.0697739	downstream-variant-500B	FAM188A	GRCh38.p7	10:15777990	TGCCATGTGGGTTCT[C/T]ATGCTTCTGGCTGGC	80013
rs137989791	snp	C/T	0.00676609	0.0577691	intron-variant	FAM188A	GRCh38.p7	10:15806008	TGCCATCACCACGTG[C/T]AGACAAATCTGAACA	80013
rs138078656	snp	G/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15787595	GTTAAAGCTATTCTT[G/T]TGAGGGTAAGCTATG	80013
rs138079791	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15842974	TCTAGGAAATGCACC[A/G]TGTTTTACCAAGAGG	80013
rs138081865	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15859711	TTATACACAGACTAC[A/C]ACGCCTAACCACATA	80013
rs138087852	in-del	-/TTAAA	0.00364368	0.0425272	intron-variant, downstream-variant-500B	FAM188A	GRCh38.p7	10:15782255	AGGACTATTAACACT[-/TTAAA]TTATATTTATATCAG	80013
rs138093779	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15800431	CCATCTCCTGATGCT[A/G]TTGTGGTGAGCTTGT	80013
rs138124154	snp	A/G	0.000199355	0.00998188	utr-variant-5-prime, missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15837296	CATCTTTTAATTCTG[A/G]TAAACTTCTGAACGA	80013
rs138166900	in-del	-/CA			intron-variant	FAM188A	GRCh38.p7	10:15795003	GAAAGTCATTCACTC[-/CA]CGTTTCAACTGTGGT	80013
rs138171275	snp	C/T	0.00199481	0.0315187	intron-variant	FAM188A	GRCh38.p7	10:15820832	AAGGAAGGTCAGGTG[C/T]CTTAGGCTCATGCCT	80013
rs138190795	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15830586	CATCTTCTTTAAATT[C/T]CACAGTACACCTGAG	80013
rs138205833	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15853698	TCTCAAGGAAAAGTA[C/T]ATGTGTAATTTTTTT	80013
rs138217727	snp	C/T	0.00279162	0.0372561	intron-variant	FAM188A	GRCh38.p7	10:15827258	TCATAAATATGAAAG[C/T]CAGCCAGGCGCGGTA	80013
rs138294411	snp	A/C	0.0023933	0.0345097	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15784903	AAAGATCTATGACAC[A/C]GAGGGCGTCTGAGCT	80013
rs138298251	snp	C/T	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15814743	GAAACTGTGTGCTGT[C/T]TGACACATGCGACAG	80013
rs138337801	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15823457	TCCGGCTGTCTACTA[A/G]TAAGCCAAGCATTAA	80013
rs138415825	snp	A/C	0.00676609	0.0577691	intron-variant	FAM188A	GRCh38.p7	10:15810565	GCCATCTTAAGCACA[A/C]CTCCCGACCCCCAAC	80013
rs138443885	snp	A/G	0.0119091	0.0762411	intron-variant	FAM188A	GRCh38.p7	10:15786742	TACTACAACACATTC[A/G]GCTGCCAAAAACACT	80013
rs138505011	snp	A/G	1.65446e-05	0.00287612	utr-variant-5-prime, missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15837266	TTCCCCACATTGAAT[A/G]CTGGTCCAAGACAGC	80013
rs138516893	in-del	-/A	0.0337553	0.125452	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15780399	GGCTTTTCAGTCCCC[-/A]AAGCAAAACTGCCTT	80013
rs138527566	snp	A/G	0.00874735	0.0655527	intron-variant	FAM188A	GRCh38.p7	10:15781347	GGCAGATCAAATTAA[A/G]AAGGAATGTTAGACC	80013
rs138529549	snp	A/G	0.00795532	0.062565	intron-variant	FAM188A	GRCh38.p7	10:15850629	AATTTTAGTCAGACC[A/G]GTTGTCTGCTCTCAA	80013
rs138539735	snp	C/T	9.95669e-05	0.00705504	missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15834604	CAATTTCGTTTTTTA[C/T]GTTTTCAATGCCCTA	80013
rs138558162	snp	C/G			utr-variant-3-prime, nc-transcript-variant	FAM188A	GRCh38.p7	10:15778517	CAATGTGTTATTTGT[C/G]AATATTTCTAATGAA	80013
rs138562228	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15848032	TGCTTTGAGAATGAT[A/C]ACTTATCACAACAGC	80013
rs138573641	snp	C/T	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15800910	ACCTTTAGATTCTAA[C/T]ATGATTTAAGAAAAA	80013
rs138719519	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15805200	TTGAAGTTAGACGAC[A/G]TTCTTGGAGGTTCTT	80013
rs138776509	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15790562	ATAGCTAAAGGCTCA[A/G]CGTCTCCGAATGTGA	80013
rs138790292	snp	A/C	0.00517822	0.0506191	intron-variant	FAM188A	GRCh38.p7	10:15854774	AGCAATACACAGCAG[A/C]CTGGGAGATCAAAAA	80013
rs138857530	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15819909	TGTTCTACCTAAAAA[C/T]TAAAGCAAAGTAAAG	80013
rs138860765	snp	A/G/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15786385	CCCCATCAAGGCACT[A/G/T]CGTTACCGTATTCGA	80013
rs138864241	snp	C/T	0.0490535	0.14873	intron-variant	FAM188A	GRCh38.p7	10:15850854	TGGAACCTGCTGACA[C/T]GTGATGTCTCCCCCC	80013
rs138882059	snp	C/T	0.00199481	0.0315187	intron-variant	FAM188A	GRCh38.p7	10:15859255	AAATAGGGGTTTATA[C/T]TTACTATGCCAAAAT	80013
rs138903339	snp	G/T	0.00199481	0.0315187	intron-variant	FAM188A	GRCh38.p7	10:15797071	TGTTAACATCTAAAC[G/T]GCTGTTCCCCTGTGA	80013
rs138917427	snp	C/T	0.00398564	0.0444627	intron-variant, downstream-variant-500B	FAM188A	GRCh38.p7	10:15782023	TGGCTGATTCTAAAA[C/T]GTGTCCTCATAGTAA	80013
rs138947226	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15792333	TGACTCATAGCTGCT[C/T]GTTAACATTTGTTAC	80013
rs138986833	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15823148	AAGGCAAGAGCTGAC[A/C]GTTTAACTTTCTGGA	80013
rs139082755	snp	A/G	0.00318978	0.0398085	intron-variant	FAM188A	GRCh38.p7	10:15793114	AATATATCTTTATCA[A/G]TCATTTTACAATAAT	80013
rs139106420	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15831247	ATTAATTTAGAGTAC[A/G]CCCAACCAATGAAAC	80013
rs139121470	snp	C/T	0.00755907	0.0610114	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15783216	TCCAGGAGCACTTTC[C/T]CGGTGCTTGCTTCTT	80013
rs139127950	snp	C/T	0.0023933	0.0345097	intron-variant	FAM188A	GRCh38.p7	10:15852228	ATTGTTTTCCCACAG[C/T]ATGTTTACAACATAC	80013
rs139232456	snp	C/G	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15848840	CTGTGAAGATCATTT[C/G]ACCTGCTTGGGCCTC	80013
rs139318985	snp	A/T	0.0174175	0.0916809	intron-variant	FAM188A	GRCh38.p7	10:15807651	GGCTTCATTCCTAAC[A/T]GAATACTTCTAGGCC	80013
rs139327073	snp	C/T	0.0023933	0.0345097	intron-variant	FAM188A	GRCh38.p7	10:15814615	GTCTCTAATTCAACA[C/T]GTTATTGCACATGAC	80013
rs139367304	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15811378	ATATATTTTTTGAAA[A/G]ATTTACTTACAAAAT	80013
rs139420940	snp	C/T	0.0182019	0.0936463	intron-variant	FAM188A	GRCh38.p7	10:15802381	AATCATGCCAGACAG[C/T]GAAGGAGAAGCAAGC	80013
rs139463765	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15861681	GTTCTCTAATTTCAA[A/G]AACATGCAGTTTCAT	80013
rs139468338	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15780040	TAAAAGAAACAGATA[C/T]AGACGACTGTCTTCT	80013
rs139510023	snp	A/G	0.00199481	0.0315187	intron-variant	FAM188A	GRCh38.p7	10:15828414	GATGCTAGGGCTGGC[A/G]TGGAAGGAAGTATAA	80013
rs139550944	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15822121	AAAAACAAATGGATA[C/T]GCTAATCACTGGTAA	80013
rs139588201	snp	A/C	0.00318978	0.0398085	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15860559	CCTTAAGGCTGAGGG[A/C]CCGGAAGTCCCCTCC	80013
rs139617894	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15824708	TCTAAAATCAGTTAC[C/T]ACCACCTAGTGTTAC	80013
rs139634789	snp	G/T	0.00119737	0.0244387	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15782618	GCAGTAGCATCACTT[G/T]TACTCAGACTAAATA	80013
rs139670458	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15812405	AGAAGGTTAAATTCA[A/G]TACAGCTTCTGATAT	80013
rs139719020	snp	A/C	0.0023933	0.0345097	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15785011	CCTCCAGATCACTTG[A/C]AGGGCTTGTTAGACC	80013
rs139754485	snp	A/G	0.0123036	0.0774623	intron-variant	FAM188A	GRCh38.p7	10:15831735	GGCTGGAGTGCCGTG[A/G]CATGATCTCAGCTCA	80013
rs139775155	snp	C/T	0.00279162	0.0372561	intron-variant	FAM188A	GRCh38.p7	10:15828968	TAACATATGGAGTAA[C/T]ACTTGCCTTGAAGGG	80013
rs139874549	snp	A/G	0.0103295	0.0711199	intron-variant	FAM188A	GRCh38.p7	10:15797856	CAAACCTTAGTTGCA[A/G]ATTTCTACATTTATT	80013
rs139936633	in-del	-/TG			intron-variant	FAM188A	GRCh38.p7	10:15816281	AAAAAAAAAAAAAAA[-/TG]AAAAAGAAAAAAAAT	80013
rs139970017	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15852189	CTGCCTTGCCTGACC[A/G]GTGTTGTATCTGTGT	80013
rs139974607	snp	C/T	0.0189856	0.0955633	intron-variant	FAM188A	GRCh38.p7	10:15841227	GAGATGCATTTTTTT[C/T]TGCAAAAATGTAGTA	80013
rs139987088	snp	A/T	0.00199481	0.0315187	intron-variant	FAM188A	GRCh38.p7	10:15849237	GCTAAAGAAAATACC[A/T]TAATTAAAGCAAAAA	80013
rs140015599	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15840266	CTAGCATCCTTGTGA[C/T]TGTTTTCCACTTGTT	80013
rs140038806	snp	G/T	0.0399052	0.1355	intron-variant	FAM188A	GRCh38.p7	10:15845727	GCCCAGCCTGGTTTT[G/T]AACTCCTGGCCTTAG	80013
rs140053936	snp	C/T	0.00716266	0.059414	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15786131	TGTCCCAATGGGAAA[C/T]GGCCCAGACCCACTT	80013
rs140087844	snp	A/G	0.00597247	0.0543191	intron-variant	FAM188A	GRCh38.p7	10:15815323	ATTTTAAAGCTTTCC[A/G]TGCTTGAGAAAAGGC	80013
rs140140984	snp	C/T	4.95005e-05	0.00497471	utr-variant-5-prime, synonymous-codon, nc-transcript-variant	FAM188A	GRCh38.p7	10:15843240	CCAAGAAGACTTCTC[C/T]GAAGAAAACAGGAGC	80013
rs140176345	snp	A/C/G	0.00716266	0.059414	intron-variant	FAM188A	GRCh38.p7	10:15798103	TCAACCTTTTTTTGC[A/C/G]GTCACCAATGAATGA	80013
rs140192525	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15794025	CACAGTGTTAACAGC[A/G]TGACTGCAAATCCAC	80013
rs140235145	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15847488	ACCTTCAGCTTTAGG[A/G]AAGTAACTTTTACAG	80013
rs140322683	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15809430	CCTGTGCAGTAGGTT[C/T]GCATGTTTTCAAGTA	80013
rs140327220	in-del	-/GAAAG			intron-variant	FAM188A	GRCh38.p7	10:15848663	AAAAAAAAAAAAAAA[-/GAAAG]AAAAATTAAATGGCA	80013
rs140342431	snp	C/T	0.00636936	0.0560724	intron-variant	FAM188A	GRCh38.p7	10:15805418	GTTATACTGGTAATA[C/T]AGATAGAGGTACCTG	80013
rs140392012	snp	A/G	0.00716266	0.059414	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15785922	TGATAAAATGACCAT[A/G]ATATCTGTTATCTAG	80013
rs140393124	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15799687	TAGCACACAGGGAAA[A/C]TGAAAAAGGTGAACA	80013
rs140400027	snp	A/G	0.0023933	0.0345097	intron-variant	FAM188A	GRCh38.p7	10:15855943	TAAAACAAATTATAT[A/G]TTCAAAGTACCAAGG	80013
rs140410032	in-del	-/TGTT	0.00318978	0.0398085	intron-variant	FAM188A	GRCh38.p7	10:15799864	ACTACGAACACTCAC[-/TGTT]TGTTAGCTAACTGCG	80013
rs140412532	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15842739	TATAAGGTGGCACCA[C/T]ACATCTCTCTGGGTA	80013
rs140459286	snp	A/G	0.00716266	0.059414	intron-variant	FAM188A	GRCh38.p7	10:15788291	AACAATTATTCATTT[A/G]TTAATATTTCTAACT	80013
rs140479373	in-del	-/T	0.0700422	0.173537	intron-variant	FAM188A	GRCh38.p7	10:15855468	AATGGCCGTTTTTCC[-/T]GATTACGTCTGAAAT	80013
rs140497047	snp	A/C	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15794794	TACTACTTATGACAA[A/C]TGTCTCCTACTTTAA	80013
rs140612762	in-del	-/AG	0.228253	0.249052	intron-variant	FAM188A	GRCh38.p7	10:15845090	GTCTCTGTTTCTCTT[-/AG]AGTGTTGATGATACA	80013
rs140616587	in-del	-/A	0.0696718	0.173152	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15861073	CTGTTTGTAAATGTT[-/A]ACAGCATTTTCATCT	80013
rs140647648	snp	A/C	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15825949	ATAAAGAAAATTATA[A/C]AATAAAAATAATCAT	80013
rs140664377	snp	C/G	0.00279162	0.0372561	intron-variant	FAM188A	GRCh38.p7	10:15823289	GGATTCCTCAGGGAC[C/G]ACAAGACCCTCTTAG	80013
rs140669741	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15822505	ACAGGTATGAAAAAT[C/T]GATGCATTTAAGGAA	80013
rs140673851	snp	C/G	0.00199481	0.0315187	intron-variant	FAM188A	GRCh38.p7	10:15850281	GCTTGTAGAGCATGT[C/G]TGTTTGAACAATATG	80013
rs140710655	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15789886	GTCAAACTAATGCTG[A/G]TGATGACTACTTTAT	80013
rs140734351	in-del	-/AC	0.00279162	0.0372561	intron-variant	FAM188A	GRCh38.p7	10:15804980	AAATCAGGGTAGGAA[-/AC]ACAGCAGACAGCCCT	80013
rs140756231	snp	C/T	0.000153988	0.00877328	missense, nc-transcript-variant, intron-variant	FAM188A	GRCh38.p7	10:15821677	GTATCTTAAAGCTTC[C/T]ATTAGTGTTAAAAAT	80013
rs140793818	snp	G/T	0.00676609	0.0577691	intron-variant	FAM188A	GRCh38.p7	10:15810355	ACCATCCTCAAATCA[G/T]GAAAGTAAATTTTGA	80013
rs140843182	snp	A/G	0.0399052	0.1355	intron-variant	FAM188A	GRCh38.p7	10:15846113	CAGGCATGAGCCACC[A/G]CGCCTGGCCGTGATT	80013
rs140855307	snp	A/T	0.000115533	0.00759957	utr-variant-5-prime, missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15843219	TATCATACCTGAACA[A/T]TCCCGCCAAGAAGAC	80013
rs140875558	snp	G/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15807089	CATGCAGATGAAAAC[G/T]GCACGCAGCTCACAG	80013
rs140898986	snp	A/C	0.00636936	0.0560724	intron-variant	FAM188A	GRCh38.p7	10:15804563	TCGTCATCTAACTTC[A/C]AGAATGACTGCACAT	80013
rs140973902	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15846488	CATTCTTCACATTCC[A/G]TAATTCCAAGGCAAG	80013
rs140988870	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15829729	GCTATAGCATGATAG[C/T]CTAGACAGGTGAGAG	80013
rs141028097	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15819815	GTTAACTGCTAAAAC[A/G]CTACAGCAATATGTA	80013
rs141088226	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15858148	CCTCTGATTCAGAGG[C/T]GATAACTTCAAAAAT	80013
rs141090298	snp	C/G	0.00676609	0.0577691	intron-variant	FAM188A	GRCh38.p7	10:15814111	AGAGCGAAATTTCCA[C/G]TATTTTTTATGTGGT	80013
rs141095100	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15825735	ATGTTTTGAAATATG[C/T]ATACACTGTAGAATG	80013
rs141133556	snp	C/T	0.00478085	0.0486577	intron-variant	FAM188A	GRCh38.p7	10:15853336	GCCCACTGGAAGTTA[C/T]AATTATTTACATGAT	80013
rs141134562	snp	G/T	0.00716266	0.059414	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15780436	AAAGTTATACACAAA[G/T]AATATAATTCAAGTT	80013
rs141243918	in-del	-/AACACAACAC	0.0372196	0.131242	intron-variant	FAM188A	GRCh38.p7	10:15795043	TCACTAGTAAAACAA[-/AACACAACAC]AACACAACACAACAC	80013
rs141258974	snp	A/G	0.00199481	0.0315187	intron-variant	FAM188A	GRCh38.p7	10:15817541	TCTGTGAACATTACT[A/G]TACCAAAAACTTGAG	80013
rs141296028	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15786873	AAAATTTAAATTGTG[A/G]TGACTTTGGAATATT	80013
rs141328240	snp	C/T	0.00716266	0.059414	intron-variant	FAM188A	GRCh38.p7	10:15790216	TGGAATTGTACACTA[C/T]CTCTATCAGAAAGGA	80013
rs141334813	snp	C/T	0.00438332	0.0466095	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15862353	GCTGATTACAATTTA[C/T]GTAATTCTTCCACTT	80013
rs141354676	snp	C/T	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15858791	TAAATGTTAACTGAT[C/T]ACAATGGAAGTAAAT	80013
rs141366806	in-del	-/T	0.227837	0.249016	intron-variant	FAM188A	GRCh38.p7	10:15800226	GTAGATACTAGTCTA[-/T]TTTTTCTACTACCAT	80013
rs141396012	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15787231	GATATATACTGTATT[A/G]GTCCAGCAGCAGCCT	80013
rs141416530	snp	A/T	0.00438332	0.0466095	intron-variant	FAM188A	GRCh38.p7	10:15826456	TTTCACTAAAGAATG[A/T]ACAAAACAATCTAGT	80013
rs141495285	snp	A/T	0.0383715	0.133092	intron-variant	FAM188A	GRCh38.p7	10:15848608	CACTGCACTCCAGCT[A/T]GGGCCACAGAGCTAG	80013
rs141501298	snp	A/T	0.00597247	0.0543191	intron-variant	FAM188A	GRCh38.p7	10:15797878	ACATTTATTCTAGTA[A/T]AAGCTTTAGCTCCCT	80013
rs141504808	snp	A/G	0.00119737	0.0244387	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15784724	CCTGGGTAAAGGAGC[A/G]AAACTCCATCTTAAA	80013
rs141513453	snp	A/G	3.3534e-05	0.00409461	missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15837217	ACCTTTGTCAGTAAT[A/G]CAGAATACAGAAAAA	80013
rs141514573	snp	C/T	0.00636936	0.0560724	intron-variant	FAM188A	GRCh38.p7	10:15829981	TGGCACAGTGTCCTG[C/T]GGTACCACTTGGCCT	80013
rs141542599	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15837423	AAACATATACATACA[A/G]ACAGGAAAGTTTTGG	80013
rs141601152	snp	G/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15845146	ATTCCAAGGATACAT[G/T]TGATATATGGTACAA	80013
rs141633823	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15801974	AATGAGGAAGATGAC[A/G]TAGAAGAAGCAGGGC	80013
rs141675097	snp	C/T	0.00517822	0.0506191	intron-variant	FAM188A	GRCh38.p7	10:15801278	TGTTTTATGCACATG[C/T]AGTCAGGGTGATGAC	80013
rs141680181	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15833064	TTATGTATCAGCTCT[C/T]CTTAACGGAATGGAT	80013
rs141737701	snp	C/G	0.00716266	0.059414	intron-variant	FAM188A	GRCh38.p7	10:15797546	ATTGTATCTAGTCTT[C/G]TGCTATTACAAAAAA	80013
rs141826605	snp	C/T	0.00279162	0.0372561	intron-variant	FAM188A	GRCh38.p7	10:15823733	CTCTGCTATCAAATA[C/T]TGAATTTACTCCATG	80013
rs141855364	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15818743	CAGAAACGAAAGGCT[A/G]TATACTACATGATTC	80013
rs141876239	snp	C/T	1.65252e-05	0.00287443	utr-variant-5-prime, synonymous-codon, nc-transcript-variant	FAM188A	GRCh38.p7	10:15841553	ACAACAAGCACTTTC[C/T]AAAATATCACACAAG	80013
rs141903607	snp	A/G	0.000153988	0.00877328	missense, intron-variant, nc-transcript-variant	FAM188A	GRCh38.p7	10:15786637	TCTAATTTATTCTTC[A/G]TGAGATTTATACTAC	80013
rs141913420	snp	A/G	0.0383715	0.133092	intron-variant	FAM188A	GRCh38.p7	10:15812177	AACTCCTGACCTCAC[A/G]TGATTCACCTGCCTC	80013
rs141919790	snp	C/T	0.00398564	0.0444627	intron-variant	FAM188A	GRCh38.p7	10:15781041	TGATTATAAAGTACC[C/T]CCTATTACAAAGCTG	80013
rs141930652	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15859293	AATCTATTTCGGGAA[C/T]AGGTGTTCCCTAAAT	80013
rs141932043	snp	C/G	0.00279162	0.0372561	intron-variant	FAM188A	GRCh38.p7	10:15815589	ACAATTCTGTATCTT[C/G]CTACGAACATTCAGC	80013
rs142027298	snp	C/T	0.00716266	0.059414	intron-variant	FAM188A	GRCh38.p7	10:15781911	TGCCAAGGGTAACGA[C/T]CTGTATGGGGGTGTA	80013
rs142052167	snp	A/T	0.00279162	0.0372561	intron-variant	FAM188A	GRCh38.p7	10:15825670	TAATATCCGTTTCTG[A/T]TTATTTTATAATTGA	80013
rs142079946	snp	A/G	0.00478085	0.0486577	intron-variant	FAM188A	GRCh38.p7	10:15820298	TCTGGGAAAGTGAGA[A/G]GACCAGTGTGGCTGG	80013
rs142094639	snp	A/G	0.00914312	0.0669923	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15783931	GAAATACCAACAAAA[A/G]GTAGTGTAGCCCACT	80013
rs142152749	in-del	-/CAAA			intron-variant	FAM188A	GRCh38.p7	10:15798789	GTCTCAAAAACAAAC[-/CAAA]AAACAAACAAAAAAC	80013
rs142156075	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15821795	TGTATAAATTTGAAA[C/T]GTACTTATATGTATA	80013
rs142283264	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15842488	ACTAAAATTTGTTTT[G/T]TATTTCACCTATTAA	80013
rs142323649	snp	G/T	0.00597247	0.0543191	intron-variant	FAM188A	GRCh38.p7	10:15795832	TTTGTTCAAAAGGTG[G/T]TATTTTTCCCTGTTT	80013
rs142331643	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15831256	GAGTACGCCCAACCA[A/G]TGAAACTTGTAATGA	80013
rs142355387	snp	A/C/T	0.000119328	0.00772347	missense, downstream-variant-500B, nc-transcript-variant	FAM188A	GRCh38.p7	10:15779011	TTTAGTGAAGGAGAG[A/C/T]GATCTGTGGTCCAGA	80013
rs142373142	snp	C/T	0.00716266	0.059414	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15779334	AAGTAAATTTGTAAA[C/T]GATATTTAATTGCTA	80013
rs142412788	snp	G/T	0.00478085	0.0486577	intron-variant	FAM188A	GRCh38.p7	10:15832331	ATAAGATACCTGGGG[G/T]TCCAGAAACAACTGG	80013
rs142497433	snp	A/G	0.00716266	0.059414	intron-variant	FAM188A	GRCh38.p7	10:15789476	ATAGTGCCTATTGCT[A/G]TTAGAGACCCTCTTC	80013
rs142501611	snp	C/T	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15836992	ACAACCAGAACATTA[C/T]TGATAATCTCTGTAG	80013
rs142607461	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15855510	AAACACCTAATCCTA[C/T]GTAGACAATTTTGTA	80013
rs142626908	in-del	-/GAT	0.0667028	0.170006	intron-variant	FAM188A	GRCh38.p7	10:15859628	TTTTTAACCGTGACA[-/GAT]AATAAACCATATAAA	80013
rs142665795	snp	C/G/T	0.000500986	0.0158199	utr-variant-5-prime, synonymous-codon, nc-transcript-variant	FAM188A	GRCh38.p7	10:15837309	TGGTAAACTTCTGAA[C/G/T]GATCTTTTTCTGGGG	80013
rs142701069	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15810650	TGTTCTATAATGTAT[C/T]TGGTCAACAAAAAGT	80013
rs142732538	snp	C/G	0.0414528	0.137958	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15782649	CACTTCCAGTATGTA[C/G]CAATACTTCCAATTT	80013
rs142738004	snp	G/T	0.0023933	0.0345097	intron-variant	FAM188A	GRCh38.p7	10:15816023	GTGATCCCAACACTT[G/T]GGGAGGCAGAGGTGG	80013
rs142742350	snp	C/T	0.00279162	0.0372561	intron-variant	FAM188A	GRCh38.p7	10:15851098	CTGAAATGCTGACCA[C/T]AAACCTGCGAAACTT	80013
rs142791633	snp	A/G	0.00716266	0.059414	intron-variant	FAM188A	GRCh38.p7	10:15792502	AGTGCTAACAGTGAC[A/G]GGAGGCCACAGCAAG	80013
rs142813643	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15803984	TTTTAGGTACCCTCA[A/G]TAGGAAGAGATCCTA	80013
rs142815049	snp	A/C	0.00676609	0.0577691	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15860543	CTCTTTAACTCCCGC[A/C]CCTTAAGGCTGAGGG	80013
rs142839462	in-del	-/AATA			intron-variant	FAM188A	GRCh38.p7	10:15827543	GTGAGACTCCGTCTC[-/AATA]AATAAATAAATAAAT	80013
rs142887008	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15784910	TATGACACCGAGGGC[A/G]TCTGAGCTGCTATAG	80013
rs142899701	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15853893	CGAGCATTCAAGCAG[C/T]AACTTGGAACACTTG	80013
rs142999951	in-del	-/CTTAAA	0.0295035	0.117819	intron-variant	FAM188A	GRCh38.p7	10:15789190	AAATGTACAATATGT[-/CTTAAA]CTTAATCGAATCTTT	80013
rs143056388	snp	A/C	0.00716266	0.059414	intron-variant	FAM188A	GRCh38.p7	10:15813581	TCCATTAAGAACAGA[A/C]CCATATCTATTTTTG	80013
rs143066352	in-del	-/T	0.0693013	0.172766	intron-variant	FAM188A	GRCh38.p7	10:15856095	AAAACAACAAAAAAA[-/T]CTTTTAAACGATGTG	80013
rs143113508	in-del	-/A	0.00597247	0.0543191	intron-variant	FAM188A	GRCh38.p7	10:15796686	AGTCAAAGCTCAATC[-/A]ACTTCTACATGTCCA	80013
rs143145333	snp	A/G	0.00517822	0.0506191	intron-variant	FAM188A	GRCh38.p7	10:15834236	CACTTACAAAGATAT[A/G]CTTATTTCTAAGTCA	80013
rs143174347	snp	C/T	0.00358779	0.0422022	intron-variant	FAM188A	GRCh38.p7	10:15793693	ATTTAGGTATGTGGC[C/T]CTGGAGAAGTGACTC	80013
rs143182055	snp	A/T	0.00716266	0.059414	intron-variant	FAM188A	GRCh38.p7	10:15811469	TGAGACTATGTATAG[A/T]TTAATATTTCTGAAA	80013
rs143233456	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15826202	TTGGATTTTATTTTA[A/G]GTGCGTAGGGAAGCC	80013
rs143312581	snp	A/G	0.0023933	0.0345097	utr-variant-3-prime, nc-transcript-variant	FAM188A	GRCh38.p7	10:15778226	ATCATAATAAATAAC[A/G]TAATATACTAATGTA	80013
rs143335540	snp	C/T	0.00716266	0.059414	intron-variant	FAM188A	GRCh38.p7	10:15822921	TGGGTCCATAATATA[C/T]CTAAAAAGCATTTCT	80013
rs143352051	snp	A/G	0.0387552	0.1337	intron-variant	FAM188A	GRCh38.p7	10:15814681	CCCCTGCCCTAGACA[A/G]AGTTCACTGGCTGCC	80013
rs143365250	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15849329	TACGGGGGTAGGATG[C/G]AGGTGCCAGCAAATG	80013
rs143370888	snp	C/G	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15784581	GAAACCCCATCTCTA[C/G]TAAGGATACAAAAAT	80013
rs143433396	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15852193	CTTGCCTGACCGGTG[G/T]TGTATCTGTGTTACT	80013
rs143433468	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15808408	ACTTTACAGCTTTTC[C/G]TTAACACCGTTTTAT	80013
rs143476276	snp	C/T	0.00676609	0.0577691	intron-variant	FAM188A	GRCh38.p7	10:15849530	TAGAGATGATGCTGA[C/T]GTAATGAAAGCAACA	80013
rs143522168	snp	A/G	0.00159617	0.0282053	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15780585	GATGCCTGGCGGCTC[A/G]GACTCCATCTCACTT	80013
rs143547422	snp	A/G	0.00399998	0.044542	intron-variant	FAM188A	GRCh38.p7	10:15797326	TAAAAACCACTTGAC[A/G]TTTTTTAACATTTGT	80013
rs143566781	snp	C/G	0.00279162	0.0372561	intron-variant	FAM188A	GRCh38.p7	10:15836203	CATTATACCCTCAAT[C/G]CCTTACACTTTTATA	80013
rs143605166	snp	A/C	0.00755907	0.0610114	intron-variant	FAM188A	GRCh38.p7	10:15812740	CAATCCCACTTATTA[A/C]GTGATGTGCATACAG	80013
rs143605867	snp	C/T	0.0402882	0.136092	intron-variant	FAM188A	GRCh38.p7	10:15827359	CCAGCCTGGCTAACA[C/T]GGTAAAATCCCGTCT	80013
rs143651330	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15790826	ATTTTGGAGGATCAA[C/T]CTTTCGGGTGAGGGA	80013
rs143762840	snp	A/T	9.95917e-05	0.00705591	missense, intron-variant, nc-transcript-variant	FAM188A	GRCh38.p7	10:15786642	TTTATTCTTCATGAG[A/T]TTTATACTACGGGGA	80013
rs143771171	snp	A/G	0.0023933	0.0345097	intron-variant	FAM188A	GRCh38.p7	10:15830608	ACACCTGAGAGGCAG[A/G]TATCTGCCCCATTCA	80013
rs143796369	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15818761	TACTACATGATTCCA[C/T]TGGTATGAAATGTAC	80013
rs143838446	snp	C/T	0.00279162	0.0372561	intron-variant	FAM188A	GRCh38.p7	10:15791349	TTTCACCAACTGACT[C/T]CCTAGAGAATAAGGA	80013
rs143851197	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15825845	TGTAATACTGATTTC[C/T]TTTTATAAAAACAAA	80013
rs143870484	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15793252	ACACTTTGAATAGAC[C/G]TGATAACTGCTTCTC	80013
rs143886221	snp	A/C	0.00676609	0.0577691	intron-variant	FAM188A	GRCh38.p7	10:15806265	CTTCCCTCATGCTAT[A/C]CAGTAACTCTGACCT	80013
rs143993474	snp	A/G	1.68809e-05	0.0029052	utr-variant-5-prime, missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15841432	ATATCTTACAAGAAT[A/G]TTCCACTTGGCAACT	80013
rs143998828	snp	C/T	0.00953873	0.0683987	intron-variant	FAM188A	GRCh38.p7	10:15828781	ACTAGGAAAAAAATA[C/T]GTTTACTAACATGAG	80013
rs144087874	snp	A/G	0.00993419	0.0697739	intron-variant	FAM188A	GRCh38.p7	10:15813034	AAGTCTTTTTTACCT[A/G]TTCCCTGGGTTATCC	80013
rs144194614	snp	C/T	0.00517822	0.0506191	intron-variant	FAM188A	GRCh38.p7	10:15853114	TATATTTAAGTTTGG[C/T]AGAAGGGAAAAAGGA	80013
rs144209273	snp	A/G	0.00199481	0.0315187	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15780272	CTACTCATTCCTAAG[A/G]AAGTGCTAAAGATAC	80013
rs144259156	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15856568	ACACTCTCCCTCAGG[C/T]GTCAGCAAACTACAA	80013
rs144267926	snp	C/T	0.00557542	0.0525036	intron-variant	FAM188A	GRCh38.p7	10:15815197	AATTGTCAGTTTTTG[C/T]AGTTCACATTGTGCT	80013
rs144353105	snp	G/T	0.00755907	0.0610114	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15779218	TGAAAACAATTTTTA[G/T]AGGCTAGCAAATAAG	80013
rs144387466	snp	G/T	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15829327	TAGAACAGTGGTTCT[G/T]AACCCTGACTACACA	80013
rs144423379	snp	A/G	0.0154538	0.0865337	intron-variant	FAM188A	GRCh38.p7	10:15788364	GACACATTAATTCAG[A/G]TGTGGCTAGTTTATG	80013
rs144479099	snp	A/G	0.00716266	0.059414	intron-variant	FAM188A	GRCh38.p7	10:15789156	CATATATGCAGATAT[A/G]GATTTTTAAAAAGGC	80013
rs144496621	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15828670	TTATATAAGGAAAGA[C/T]GTATATACAAAACAT	80013
rs144555557	snp	G/T	0.00914312	0.0669923	intron-variant	FAM188A	GRCh38.p7	10:15789983	TGAAATGAGAGTGGT[G/T]TTAAACAAAAGTTGT	80013
rs144559410	snp	A/C	0.0146672	0.084371	intron-variant	FAM188A	GRCh38.p7	10:15831873	TAGAGACGGGGTTTC[A/C]CTGTGTTGGCCAGGC	80013
rs144579480	snp	C/G	0.00993419	0.0697739	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15785166	CATGCTCGTGGGAGG[C/G]AAACAGCATGAACTA	80013
rs144611478	snp	C/T	4.95029e-05	0.00497484	utr-variant-5-prime, synonymous-codon, nc-transcript-variant	FAM188A	GRCh38.p7	10:15843222	CATACCTGAACAATC[C/T]CGCCAAGAAGACTTC	80013
rs144636934	snp	C/T	0.00318978	0.0398085	intron-variant	FAM188A	GRCh38.p7	10:15843083	CTGTTCATGAAACTT[C/T]CTAAAACATTTTAAA	80013
rs144714226	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15851002	GATAAGTGAACCAAA[C/T]TCATTCTCACCCAAG	80013
rs144761297	snp	A/T	0.00676609	0.0577691	intron-variant	FAM188A	GRCh38.p7	10:15805031	AACACAGACTCTAAA[A/T]GCACAAGTGGAAATA	80013
rs144772521	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15803639	CATAAAACCATAATT[C/T]CTTAAACATTTGGCA	80013
rs144800286	snp	C/T	0.00517822	0.0506191	intron-variant	FAM188A	GRCh38.p7	10:15800877	TATGTAAGTGCAGGG[C/T]TGCTATAGGAAAGGC	80013
rs144800311	snp	C/T	0.0146672	0.084371	intron-variant	FAM188A	GRCh38.p7	10:15846880	AGGTGCCCACCACCA[C/T]GCCCGGCTAGTTTTT	80013
rs144801739	snp	C/T	0.00676609	0.0577691	intron-variant	FAM188A	GRCh38.p7	10:15811958	TTATTTTTATTTTTT[C/T]TGAGATGGAGTCTTG	80013
rs144807839	snp	A/T	0.00597247	0.0543191	intron-variant	FAM188A	GRCh38.p7	10:15840771	CTAGCTGTCTCCATT[A/T]CACACTGGCAGCTTT	80013
rs144834137	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15807182	TACAGACAACATTCA[A/G]TAAACACTCACAGTA	80013
rs144984572	in-del	-/T	0.0622301	0.165053	intron-variant	FAM188A	GRCh38.p7	10:15857597	AGAGAGAAGAATAAA[-/T]TTTCACGTTAAAATA	80013
rs145026603	snp	C/T	0.00676609	0.0577691	intron-variant	FAM188A	GRCh38.p7	10:15813168	CAATTTTTAACAAGT[C/T]TAGTTGTCCTAACTC	80013
rs145029104	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15787063	ACAGGGTCAAAAGGC[A/G]GTGGTACATCAGATA	80013
rs145122284	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15862461	TGACTTTCTCCATTA[A/G]TGTATGTAAATATTA	80013
rs145180921	snp	A/G	0.00755907	0.0610114	intron-variant	FAM188A	GRCh38.p7	10:15822412	AAGTGATAACAGGGA[A/G]TTGAATCTTGAAGCG	80013
rs145190176	in-del	-/AAAC	0.0707826	0.174302	intron-variant	FAM188A	GRCh38.p7	10:15792700	TTTAGCAACTTAACA[-/AAAC]AAACAGCTTCAGATT	80013
rs145212197	snp	A/G	0.00993419	0.0697739	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15785646	AGACCAAAGTTTTAA[A/G]AAGTCCAGTAGTCTA	80013
rs145213574	snp	C/T	0.030278	0.119257	intron-variant	FAM188A	GRCh38.p7	10:15807709	ATTATTTGGATACTA[C/T]TGTAAGAGAAAAAGA	80013
rs145244275	snp	A/G	0.00755907	0.0610114	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15783218	CAGGAGCACTTTCCC[A/G]GTGCTTGCTTCTTCA	80013
rs145250560	snp	C/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15824742	TAGATACTACATCAT[C/G]TATTTCCCTGGACTT	80013
rs145286799	snp	A/C/G	0.000198523	0.00996113	utr-variant-5-prime, missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15837263	TATTTCCCCACATTG[A/C/G]ATACTGGTCCAAGAC	80013
rs145305510	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15805802	CAGGCAGAAGCTACT[C/T]CTTCAGCCCAGATCT	80013
rs145311817	snp	C/T	0.00015208	0.00871876	utr-variant-5-prime, missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15860247	TCCGAGAGACCGGGG[C/T]TGCTCTTGGTGCCCC	80013
rs145394651	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15822865	AAGTCTTTTCATAAA[C/T]GATACCCTTCAGCTA	80013
rs145397956	snp	A/T	0.00348313	0.0415865	utr-variant-5-prime, missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15841430	ATATATCTTACAAGA[A/T]TGTTCCACTTGGCAA	80013
rs145409874	snp	G/T	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15832163	AACCACACTGATGAG[G/T]ACCAAGTGTGAGAGA	80013
rs145424155	in-del	-/A	0.0287284	0.116357	intron-variant	FAM188A	GRCh38.p7	10:15820949	ACCCTGTCTCTATTT[-/A]AAAAAATTTTTTTAA	80013
rs145474329	snp	C/T	0.00199481	0.0315187	intron-variant	FAM188A	GRCh38.p7	10:15809576	CTCCATCGTACTTAA[C/T]AGGAATTAAGTTTCC	80013
rs145499136	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15817268	CTCAAACCCTAAAAC[A/T]ATAAACTTGACGATA	80013
rs145582380	snp	A/C	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15780465	TTATTAAGTTAAATA[A/C]AATCGGCCCTATTTT	80013
rs145600126	in-del	-/ATA	0.029116	0.117091	intron-variant	FAM188A	GRCh38.p7	10:15810637	GGATCTACAGTGTGT[-/ATA]TCTATAATGTATTTG	80013
rs145671145	snp	C/G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15823444	GCATATATGAAGATC[C/G/T]GGCTGTCTACTAATA	80013
rs145732076	snp	C/T	0.00755907	0.0610114	intron-variant	FAM188A	GRCh38.p7	10:15846147	AAACTTAATTACTAC[C/T]TCAAAGGTATAGAAA	80013
rs145753005	snp	A/C	0.00636936	0.0560724	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15784024	ATACCTAGTGTATGA[A/C]CTTAAACAATTGTCT	80013
rs145766780	snp	A/G	0.00716266	0.059414	intron-variant	FAM188A	GRCh38.p7	10:15829899	AGCAGTTTGCCCACC[A/G]TCAAACAGCAGAGGC	80013
rs145776875	snp	A/C	0.00119737	0.0244387			GRCh38.p7	10:15786718	TTTCTTTCATGATTA[A/C]ATTACTGGTACTACA	80013
rs145790227	snp	C/G	0.00318978	0.0398085	intron-variant	FAM188A	GRCh38.p7	10:15781317	TCCACAATTTAGATA[C/G]ATGAAGTCAGCATGG	80013
rs145795997	snp	C/T	0.00835141	0.0640778	intron-variant	FAM188A	GRCh38.p7	10:15850330	GCAACAGGATGGCTG[C/T]AGTGTTCAGGGAACA	80013
rs145816571	snp	C/G	0.00159617	0.0282053	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15784817	TAATTGCCAAAAGGA[C/G]TGTTGAGTCACTATG	80013
rs145853135	snp	C/G	0.00358779	0.0422022	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15786344	TATGTGTATAGACTG[C/G]TGTCTGCGTCATCTT	80013
rs145855276	snp	G/T	0.00318978	0.0398085	intron-variant	FAM188A	GRCh38.p7	10:15858281	TCCTTTATTTTGAAA[G/T]GGTACTGATGGAACT	80013
rs145866878	snp	A/G	0.00318978	0.0398085	intron-variant	FAM188A	GRCh38.p7	10:15798412	TGACAGTTCAGGAGT[A/G]TAAAAAGAATTTAAA	80013
rs145939188	snp	C/T	0.00279162	0.0372561	intron-variant	FAM188A	GRCh38.p7	10:15837005	TATTGATAATCTCTG[C/T]AGTCCAAAAGAGCAG	80013
rs145943219	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15830641	GAGAAGAAGCTGAGA[C/T]TGAGATTTTAATCCA	80013
rs145950391	snp	C/G	0.00199481	0.0315187	intron-variant	FAM188A	GRCh38.p7	10:15831344	TTATCCAGGAAAAAC[C/G]AAGAAGGTTCAGTGA	80013
rs146056602	snp	G/T	0.0023933	0.0345097	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15785010	GCCTCCAGATCACTT[G/T]CAGGGCTTGTTAGAC	80013
rs146067913	snp	C/T	0.00914312	0.0669923	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15782917	AAGATCACGTTCAAC[C/T]CTCTTAACCTGGCGT	80013
rs146073708	snp	C/T	0.00279162	0.0372561	intron-variant	FAM188A	GRCh38.p7	10:15851677	TGACCTTAAATACTG[C/T]TGAGTTTCCAACCAC	80013
rs146181779	snp	A/C	0.00835141	0.0640778	intron-variant	FAM188A	GRCh38.p7	10:15801746	CCATCACTGTTACAG[A/C]AAAAGCTAATCCATC	80013
rs146191219	snp	A/C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15798102	CTCAACCTTTTTTTG[A/C/T]GGTCACCAATGAATG	80013
rs146275703	snp	A/C	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15852226	TCATTGTTTTCCCAC[A/C]GTATGTTTACAACAT	80013
rs146300064	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15820803	CTGCTATGGAACCCT[C/G]TTCTAAAATAGAAAA	80013
rs146301272	snp	C/T	0.0107246	0.0724382	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15779658	TGTTTGTCAACAAAA[C/T]TTGCTATTATGGTAT	80013
rs146321227	snp	A/G	0.00716266	0.059414	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15782508	TGTGCATGTATCACT[A/G]TAACTTTTTTCAAAA	80013
rs146332995	snp	A/G	0.0444908	0.142359	intron-variant	FAM188A	GRCh38.p7	10:15799449	TGATCCACCCACCTC[A/G]GGTTCCTAAAGTGCT	80013
rs146400905	in-del	-/GGA	0.0379877	0.132479	intron-variant	FAM188A	GRCh38.p7	10:15829164	CATAGATGATCAGAG[-/GGA]GGAGAAAACTTTTCC	80013
rs146506030	snp	C/T	0.00953873	0.0683987	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15780295	AAAGATACATTGTAA[C/T]GTGAAATACATTTTT	80013
rs146509845	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15849189	CTTGAACAGGAATTT[G/T]CCAGAGAGGCAAAGG	80013
rs146519926	snp	A/G	0.00716266	0.059414	intron-variant	FAM188A	GRCh38.p7	10:15846370	AATTTACATATGGAC[A/G]TAACAAGGAATCTTC	80013
rs146571104	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15826005	ACAATATGGACAAAA[A/G]TAATGTACAAATACT	80013
rs146625460	snp	C/T	0.0170251	0.090679	intron-variant	FAM188A	GRCh38.p7	10:15793945	GAAGATGTGGTCTCA[C/T]AGAGGCAATGCTATA	80013
rs146635937	snp	A/G	0.00318978	0.0398085	intron-variant	FAM188A	GRCh38.p7	10:15790137	CATGGAGAACAAGAT[A/G]TCCAAAAGCCCTGCT	80013
rs146690446	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15847450	AAATTTGAAAAAGTT[A/G]TAAGCCAGAAAAATA	80013
rs146739935	snp	C/T	0.0189856	0.0955633	intron-variant	FAM188A	GRCh38.p7	10:15849339	GGATGGAGGTGCCAG[C/T]AAATGGGCGGCAGGA	80013
rs146746973	snp	C/T	0.0023933	0.0345097	intron-variant	FAM188A	GRCh38.p7	10:15812892	CCTCCGCTGCCAATC[C/T]AATCCATCACCCAGT	80013
rs146759173	snp	A/C	0.00199481	0.0315187	intron-variant	FAM188A	GRCh38.p7	10:15809177	GAAGAATCAATGAGG[A/C]AAACGATGGTTAGGG	80013
rs146762995	snp	A/G	0.0387552	0.1337	intron-variant	FAM188A	GRCh38.p7	10:15850823	ACTTGCTGGTTTTGC[A/G]GCTCAGGGGGCATCA	80013
rs146831629	in-del	-/AGA			intron-variant	FAM188A	GRCh38.p7	10:15787335	AAGGAAGAAGAAGGC[-/AGA]AGAAGGCAGACTGCA	80013
rs146848572	in-del	-/TATCTT	0.0376037	0.131863	intron-variant	FAM188A	GRCh38.p7	10:15803735	AAAAACATGCTACTC[-/TATCTT]TACTTCCAAGAATCT	80013
rs146870450	snp	A/G	0.0162398	0.0886349	intron-variant	FAM188A	GRCh38.p7	10:15828834	CTGGACTTGTTTCCT[A/G]CTCTGACAACATAGT	80013
rs146880678	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15825937	TATCCCTATCCCATA[A/G]AGAAAATTATAAAAT	80013
rs146893724	snp	C/T	0.0023933	0.0345097	intron-variant	FAM188A	GRCh38.p7	10:15811106	TAATGCAAATGAACA[C/T]GGGCCACAAGCTTCG	80013
rs146893857	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15853378	ATGATTTGCCCCTTT[C/T]GCTGTGTTGACATTC	80013
rs146927301	snp	A/T	0.00597247	0.0543191	intron-variant	FAM188A	GRCh38.p7	10:15818306	AGTGTGTATTTAAAT[A/T]AAGGTAGAAGTAAAA	80013
rs146937166	snp	A/G	0.00199481	0.0315187	intron-variant	FAM188A	GRCh38.p7	10:15814219	TTATTTACCATTTAG[A/G]TGAACTTCCAGCTTT	80013
rs146999592	snp	A/G	0.0252325	0.109451	intron-variant	FAM188A	GRCh38.p7	10:15826915	AGCCAAACATTAAAA[A/G]ACAAAAAGCCCACAA	80013
rs147043555	snp	C/T	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15830097	GTTTTCAAATAAAGC[C/T]TGTTGAATAAAGTAA	80013
rs147071653	in-del	-/T	0.0298908	0.118541	intron-variant	FAM188A	GRCh38.p7	10:15813023	AGAACTAGAGAAGTC[-/T]TTTTTTACCTATTCC	80013
rs147104542	snp	C/G	0.000577391	0.0169812	intron-variant	FAM188A	GRCh38.p7	10:15847851	AAGGAGTTGGTAAAG[C/G]AGTCTATGTTACCTG	80013
rs147159038	snp	G/T	0.00358779	0.0422022	intron-variant	FAM188A	GRCh38.p7	10:15824769	ACTTTTAAACAAATG[G/T]CTAATAATAATATCA	80013
rs147192261	snp	A/C	0.00716266	0.059414	intron-variant	FAM188A	GRCh38.p7	10:15788012	TCATGATTCAAGGTA[A/C]GTTTTCCATCTGATA	80013
rs147201269	snp	A/C	0.0379877	0.132479	intron-variant	FAM188A	GRCh38.p7	10:15827364	CTGGCTAACATGGTA[A/C]AATCCCGTCTCTACT	80013
rs147201728	snp	C/T	0.0023933	0.0345097	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15785799	AAATTTTCCCTCTTG[C/T]TTTTAAATTTTTTCT	80013
rs147208753	snp	G/T	0.0513262	0.151752	intron-variant	FAM188A	GRCh38.p7	10:15791821	GGGAGGAAACCTGAG[G/T]TGGGCTTTCAAAGGA	80013
rs147264078	snp	A/G	0.0267878	0.112589	intron-variant	FAM188A	GRCh38.p7	10:15846059	AACACCTGACCTCAG[A/G]TGATCTACCTGCCTC	80013
rs147299110	snp	A/G	0.00676609	0.0577691	intron-variant	FAM188A	GRCh38.p7	10:15806506	CAAATTAGTCACAGT[A/G]CTCACATTTATAATT	80013
rs147307524	snp	A/C/T	0.00318978	0.0398085	intron-variant	FAM188A	GRCh38.p7	10:15802863	GTCATATACTACTAA[A/C/T]AGCTAATTTGGTCAA	80013
rs147341425	snp	A/G	0.0166325	0.0896639	intron-variant	FAM188A	GRCh38.p7	10:15845902	ATCTCGGCTCACTGC[A/G]ACCTCCACCTTCTGG	80013
rs147371229	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15860554	CCGCCCCTTAAGGCT[C/G]AGGGCCCGGAAGTCC	80013
rs147404137	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15824663	GTAAAAAAGAATACA[C/T]ACATTGGGAAACAGT	80013
rs147474942	snp	A/C/T	0.00319098	0.0398384	intron-variant	FAM188A	GRCh38.p7	10:15807379	ACGAATGGTGGAAGG[A/C/T]TGGACCAGGAATGCT	80013
rs147515288	in-del	-/GT			intron-variant	FAM188A	GRCh38.p7	10:15817768	AATTCCAAGTGGCTG[-/GT]TTTGTGGCAGTCAGG	80013
rs147524178	snp	C/T			utr-variant-3-prime, nc-transcript-variant	FAM188A	GRCh38.p7	10:15778340	AGTGTATTTGGCAAT[C/T]ACACAGTAAAAGTTA	80013
rs147573204	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15818476	AGTTAAAAATAGAAT[C/T]ACTGTATGACCAGTA	80013
rs147579602	snp	C/G	0.00755907	0.0610114	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15783860	AATAACCATTTTCCT[C/G]TAACTGAATATAATT	80013
rs147589389	snp	A/G	0.00358779	0.0422022	intron-variant	FAM188A	GRCh38.p7	10:15781025	GTAGGTGAATAATTA[A/G]TGATTATAAAGTACC	80013
rs147589681	snp	A/T			intron-variant	FAM188A	GRCh38.p7	10:15822502	CAAACAGGTATGAAA[A/T]ATCGATGCATTTAAG	80013
rs147611137	in-del	-/AAAG	0.0383715	0.133092	intron-variant	FAM188A	GRCh38.p7	10:15821324	TCTTCGTTAGGTAAT[-/AAAG]AAACAGTGCTTTCTT	80013
rs147634279	in-del	-/A	0.0295035	0.117819	intron-variant	FAM188A	GRCh38.p7	10:15835339	TTGTTCTATTCACTT[-/A]AACTTTAGCCATTGT	80013
rs147679511	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15833838	AAAGTTAGGGAAAAC[C/T]TTACATTTTCAATTT	80013
rs147685594	snp	A/C	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15799009	TTTTTCTGTAATGGG[A/C]CACAGAGTAAATTTT	80013
rs147695290	snp	A/G	4.9953e-05	0.0049974	utr-variant-5-prime, synonymous-codon, nc-transcript-variant	FAM188A	GRCh38.p7	10:15841448	TTCCACTTGGCAACT[A/G]GACTCTGCAGGACTC	80013
rs147696405	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15795537	TGAGTTAGCTATAAT[A/G]AAGTCTTAACCGTTA	80013
rs147782567	snp	A/C	0.00716266	0.059414	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15784117	CTAGTGTATGACCTT[A/C]AACAATCGTCTTAAG	80013
rs147784316	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15853132	AAGGGAAAAAGGAAT[A/G]ATAGTTTGAAGGGTA	80013
rs147888432	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15799639	TCTAGCTAGAAGGAA[C/T]GGAATCAGGAAAGGC	80013
rs147889622	snp	A/C	1.64988e-05	0.00287213	utr-variant-5-prime, missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15843233	AATCCCGCCAAGAAG[A/C]CTTCTCCGAAGAAAA	80013
rs147904799	snp	G/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15803668	CAGGCTTAATAGATG[G/T]TAGAGAAAAACCCAG	80013
rs147953306	snp	C/G	0.000199048	0.00997418	missense, downstream-variant-500B, nc-transcript-variant	FAM188A	GRCh38.p7	10:15779117	CAAAACCCATCACAA[C/G]TGCAGTCCCTTCTAC	80013
rs147975316	in-del	-/AAAC	0.492386	0.0612297	intron-variant	FAM188A	GRCh38.p7	10:15798781	AAGACTCTGTCTCAA[-/AAAC]AAACAAACAAACAAA	80013
rs147987726	in-del	-/AC			intron-variant	FAM188A	GRCh38.p7	10:15822336	ATGTGGTCTCTCTGT[-/AC]ACACACACACACGGA	80013
rs148001216	snp	A/C	0.00676609	0.0577691	intron-variant	FAM188A	GRCh38.p7	10:15810329	TTCACTGGACAGAAG[A/C]AATTTTCTTAACCAT	80013
rs148099696	snp	C/T	0.00716266	0.059414	intron-variant	FAM188A	GRCh38.p7	10:15791048	ACATTTTTAAGGTAG[C/T]TATGAGATTTACAAC	80013
rs148127508	snp	C/T	0.00199481	0.0315187	intron-variant	FAM188A	GRCh38.p7	10:15858580	ACTCTGTAAGGTCTA[C/T]TATCTGTACTTTACA	80013
rs148141305	snp	C/T	0.000153988	0.00877328	missense, intron-variant, nc-transcript-variant	FAM188A	GRCh38.p7	10:15816915	TCAAGTAAGAACCAA[C/T]CTAGAACAAATGTAG	80013
rs148162120	snp	A/C	0.00676609	0.0577691	intron-variant	FAM188A	GRCh38.p7	10:15806266	TTCCCTCATGCTATC[A/C]AGTAACTCTGACCTT	80013
rs148233761	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15830677	TTCTGTCCGTGGTAC[A/G]GAGTTAGTAAATGAG	80013
rs148311594	snp	A/G	0.00318978	0.0398085	intron-variant	FAM188A	GRCh38.p7	10:15826207	TTTTATTTTAAGTGC[A/G]TAGGGAAGCCAGCCA	80013
rs148327139	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15787211	CGTCATGAATGACAG[C/T]GACTGATATATACTG	80013
rs148373967	snp	A/T	0.0260105	0.111035	intron-variant	FAM188A	GRCh38.p7	10:15844978	TTTCACCCCTGAATC[A/T]TAGTGTTTTTCTAAT	80013
rs148379819	snp	C/G	0.00398564	0.0444627	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15784624	CATATGTAGTCCCAG[C/G]TACACAGGAGGCTGA	80013
rs148391463	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15828674	ATAAGGAAAGACGTA[C/T]ATACAAAACATGTTT	80013
rs148435730	snp	C/T	1.69735e-05	0.00291315	intron-variant	FAM188A	GRCh38.p7	10:15789336	TAGGGGGGAAAAAAT[C/T]AGAAACAACTTGAAA	80013
rs148485895	snp	G/T	0.00755907	0.0610114	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15785226	TGGAGAGTGTCTTCA[G/T]AATAGCAGGCAACAA	80013
rs148488516	snp	A/G	0.00874735	0.0655527	intron-variant	FAM188A	GRCh38.p7	10:15855376	TTTGAATTTCTCAGG[A/G]CACAGCATTACTTTT	80013
rs148530209	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15812125	TTTTGTATTCTTAGT[A/T]GAGATGGGTTTTGCC	80013
rs148540122	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15851079	AACCTTCCAAAGAAT[C/G]AATCTGAAATGCTGA	80013
rs148549085	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15798671	TGTTAACCCAGCTAC[C/T]TGGGAGGCTGAGGCA	80013
rs148645072	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15825192	GGAAATGTTCATTAC[A/G]GCATTTTGGATTTCA	80013
rs148667857	snp	C/T	1.6656e-05	0.00288578	utr-variant-5-prime, missense, nc-transcript-variant	FAM188A	GRCh38.p7	10:15841447	GTTCCACTTGGCAAC[C/T]AGACTCTGCAGGACT	80013
rs148685915	snp	A/C	0.00914312	0.0669923	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15783003	TCTGCCTGGATAGAT[A/C]CCCCTTGTCTTCCTG	80013
rs148696823	snp	C/T	3.38003e-05	0.00411084	intron-variant	FAM188A	GRCh38.p7	10:15821605	AAACAGTATCCACAA[C/T]AGTGGACATCTAAAC	80013
rs148739895	snp	C/T	0.00716266	0.059414	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15779266	ATGAAACTTGACATG[C/T]AATTTTATTTTGCTA	80013
rs148759623	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15832188	GAGAGAGAGTGATGC[A/G]CTAAAGACAGTGTGG	80013
rs148847716	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15780568	GGCCTCAATCAGGCT[C/T]GGATGCCTGGCGGCT	80013
rs148850599	in-del	-/AAG	0.0433465	0.140692	intron-variant	FAM188A	GRCh38.p7	10:15816610	CTAAAGCTCTAAAGA[-/AAG]AAGAAGAAATTATAA	80013
rs148868668	snp	C/T	0.0252325	0.109451	intron-variant	FAM188A	GRCh38.p7	10:15836170	TAAGGCTCAACTACT[C/T]AGAGCTCCCCAAACC	80013
rs148877487	snp	C/T	0.0023933	0.0345097	intron-variant	FAM188A	GRCh38.p7	10:15849347	GTGCCAGCAAATGGG[C/T]GGCAGGAAAGATGAC	80013
rs148964085	snp	G/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15790702	TCTAGAAATGTTTTA[G/T]ATTTCAAATTTTTTC	80013
rs149013629	snp	A/G	0.0170251	0.090679	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15786405	ACCGTATTCGAACAC[A/G]CATTCCCTCTGTCTG	80013
rs149016326	snp	C/G	0.00279162	0.0372561	intron-variant	FAM188A	GRCh38.p7	10:15858317	TGTTAAAGAATTTCT[C/G]CATGATTAAAGGTGG	80013
rs149057648	snp	C/T	0.00597247	0.0543191	intron-variant	FAM188A	GRCh38.p7	10:15813344	CATGAATTTGCTCTA[C/T]TTGTCATGTAGAGAA	80013
rs149109455	snp	A/G	0.0023933	0.0345097	intron-variant	FAM188A	GRCh38.p7	10:15808104	GAGAATAATTAAGCT[A/G]TCCAGATGTCTACCC	80013
rs149174662	snp	C/G	0.00358779	0.0422022	intron-variant	FAM188A	GRCh38.p7	10:15826124	GGAATAGTACGAAAT[C/G]AAGATGGATGGCAGG	80013
rs149227341	snp	C/G	0.0023933	0.0345097	intron-variant	FAM188A	GRCh38.p7	10:15822907	TATAATAATATATTT[C/G]GGTCCATAATATATC	80013
rs149237842	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15844176	GCACTTAGCACAGTA[C/T]CTGGCACCAATAAAC	80013
rs149283158	snp	G/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15828510	ACTCTGAGAAAATAT[G/T]TAAAATACTGAATTG	80013
rs149333999	snp	A/G	0.00438332	0.0466095	intron-variant	FAM188A	GRCh38.p7	10:15797155	TTACTCTGTTCACAG[A/G]TGAAGAAACTAAGAA	80013
rs149351128	snp	C/T	0.00119737	0.0244387	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15785031	CTTGTTAGACCACAT[C/T]GCTGCACCCACCCTT	80013
rs149406590	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15850984	TTGGGTGCTGGTTCC[C/T]CCGATAAGTGAACCA	80013
rs149449760	snp	G/T	0.00676609	0.0577691	intron-variant	FAM188A	GRCh38.p7	10:15806030	ATCTGAACAATGTCA[G/T]TAGTCACACACTCCT	80013
rs149459406	snp	C/T	0.00199481	0.0315187	intron-variant	FAM188A	GRCh38.p7	10:15847789	TTACTATATGGAGTA[C/T]AGACATTAGAAAACG	80013
rs149493913	snp	A/C/T	0.00159649	0.0282165	intron-variant	FAM188A	GRCh38.p7	10:15793126	TCAATCATTTTACAA[A/C/T]AATTCCTATAAAACA	80013
rs149501514	snp	A/C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15800765	ATCCAGCATAAATAT[A/C/T]GTAAAGAAAGAAAAG	80013
rs149549293	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15859714	TACACAGACTACCAC[A/G]CCTAACCACATAATG	80013
rs149565708	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15821014	AATCATGACATCTTA[A/C]GAAGTGCAAGTCAAT	80013
rs149583944	in-del	-/T			intron-variant, downstream-variant-500B	FAM188A	GRCh38.p7	10:15782477	TTCAGAACTAACTTA[-/T]TTTTTTTTTTAATTA	80013
rs149607372	snp	A/C/G	0.00318978	0.0398085	utr-variant-3-prime, nc-transcript-variant	FAM188A	GRCh38.p7	10:15778642	AATGAAATAAAACCC[A/C/G]AAAGTAGTTTATCAA	80013
rs149617105	snp	G/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15815136	AGTCAGAATTAATTT[G/T]CTTTTATGGTAATTT	80013
rs149712885	snp	A/C	0.0240643	0.107019	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15780437	AAGTTATACACAAAG[A/C]ATATAATTCAAGTTA	80013
rs149756175	in-del	-/TAA	0.0618563	0.164627	intron-variant, cds-indel	FAM188A	GRCh38.p7	10:15857928	TTGCTTCCAGAAAAC[-/TAA]TGAGACTGCAGTTGT	80013
rs149768344	snp	A/G	0.00318978	0.0398085	intron-variant	FAM188A	GRCh38.p7	10:15846115	GGCATGAGCCACCAC[A/G]CCTGGCCGTGATTCT	80013
rs149820545	snp	C/G	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15840505	AGTCCAGGGAGGCAA[C/G]AGCACCTTATAGATA	80013
rs149864164	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15798204	ACAGAAGAAAAGGGA[A/G]TATCAGGTTACTTTT	80013
rs149883200	snp	C/T	0.00716266	0.059414	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15786173	CTCCAGGAGCTTAGC[C/T]TCACTAGCTAGGGGC	80013
rs149978025	snp	A/G	0.00676609	0.0577691	intron-variant	FAM188A	GRCh38.p7	10:15807689	CAGTATTTTATCTTT[A/G]GACAATTATTTGGAT	80013
rs149987586	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15848919	TATAAATTCCATTAA[C/T]TGTTACTATTCAGAC	80013
rs150050872	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15862015	TGCATGCCAAACTTT[C/T]TCCAGTCATTACAAT	80013
rs150064223	snp	C/T	0.00014872	0.00862193	utr-variant-5-prime, missense, intron-variant, nc-transcript-variant	FAM188A	GRCh38.p7	10:15847932	ATCCCTCTGATTCAC[C/T]AAACACAAACCCTAA	80013
rs150084565	snp	A/C	0.00279162	0.0372561	intron-variant	FAM188A	GRCh38.p7	10:15810535	TATTGAATTCTGATG[A/C]TCCAAGACTATTCAG	80013
rs150118445	snp	C/T	0.00011553	0.00759944	synonymous-codon, nc-transcript-variant	FAM188A	GRCh38.p7	10:15833661	TCTATCACCATCCCA[C/T]ACATTAGAAACAGCA	80013
rs150155480	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15835290	CTTATTGTAACCTCA[C/T]CAATTCCAGAAGGAC	80013
rs150206942	snp	C/G	0.00199481	0.0315187	intron-variant	FAM188A	GRCh38.p7	10:15829733	TAGCATGATAGTCTA[C/G]ACAGGTGAGAGTAAT	80013
rs150227604	in-del	-/T	0.040671	0.13668	intron-variant	FAM188A	GRCh38.p7	10:15840405	TATTCCTTGCAAATG[-/T]TACTACTATTAGAAT	80013
rs150249147	snp	A/G	0.00716266	0.059414	intron-variant	FAM188A	GRCh38.p7	10:15790452	ACTGAGAATAAAGAC[A/G]ACCTTGGTTGAAGGC	80013
rs150252297	snp	C/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15819827	AACACTACAGCAATA[C/T]GTAAACAGAAGAATA	80013
rs150292529	snp	G/T	0.000399281	0.0141238	downstream-variant-500B	FAM188A	GRCh38.p7	10:15777849	CACGTGGCTTTACAC[G/T]TGGAGGAAAAAAAGT	80013
rs150296277	snp	A/G/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15847503	AAAGTAACTTTTACA[A/G/T]ACTGAAATAATGAAA	80013
rs150364484	snp	C/G	0.00716266	0.059414	intron-variant	FAM188A	GRCh38.p7	10:15799710	GGTGAACAGGACTGA[C/G]AACTGTGACAGAAAA	80013
rs150417041	snp	A/C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15794838	AGTATCTTTGCAGCA[A/C/T]TGATGAAATTTTTTC	80013
rs150464025	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15853676	TGGGTATGATGGTCA[A/G]AAGTTATCTCAAGGA	80013
rs150525820	snp	C/T	0.00716266	0.059414	intron-variant	FAM188A	GRCh38.p7	10:15797714	TTTTCTGATACATTA[C/T]CAATACAGCCTTAGC	80013
rs150572760	snp	C/T	0.00199481	0.0315187	intron-variant	FAM188A	GRCh38.p7	10:15855682	ACATTTTGCACACCA[C/T]TTTGACAACTATACC	80013
rs150622953	snp	C/T	0.00597247	0.0543191	intron-variant	FAM188A	GRCh38.p7	10:15824059	AGGTTGATTCCCTAG[C/T]TTTGCTACTGTGAAT	80013
rs150636122	snp	C/T	0.000645925	0.0179595	utr-variant-5-prime, synonymous-codon, nc-transcript-variant	FAM188A	GRCh38.p7	10:15841586	ATGACAAAGGAGTTC[C/T]TTCTGCTCTTCCTCT	80013
rs150641745	snp	C/T	0.00755907	0.0610114	intron-variant	FAM188A	GRCh38.p7	10:15812192	GTGATTCACCTGCCT[C/T]GGCCTCCCAAAGTGT	80013
rs150684270	snp	A/G	0.0023933	0.0345097	intron-variant	FAM188A	GRCh38.p7	10:15839361	ACTGCGAACAACTGT[A/G]CATTACCAACAAGCC	80013
rs150735349	snp	C/T	0.00398564	0.0444627	intron-variant	FAM188A	GRCh38.p7	10:15830883	GGTTTGTGGCCTGGT[C/T]GTTACACATCACGAT	80013
rs150752948	in-del	-/TC	0.0325976	0.123435	intron-variant	FAM188A	GRCh38.p7	10:15856465	AATAGCAAAAATAAA[-/TC]TCTCTCTGACTAGTC	80013
rs150779808	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15792681	AATATGGCTGTCAAC[A/G]TATTTTAGCAACTTA	80013
rs150830444	snp	C/G	0.0023933	0.0345097	intron-variant	FAM188A	GRCh38.p7	10:15787361	GACTGCAGTTTAATG[C/G]GTTTAAAAATGAAAA	80013
rs150833228	snp	C/T	0.00597247	0.0543191	intron-variant	FAM188A	GRCh38.p7	10:15859472	GTTACTAGTATAAAG[C/T]GCCCAGCCTGTTACA	80013
rs150852788	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15848687	ATTAAATGGCATTGT[A/T]GACAGTACATGTGTT	80013
rs150895087	snp	A/G	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15802105	TCTACTGTTGGTTAC[A/G]GTAAGGCTTCCAGCC	80013
rs150905449	snp	G/T	0.00636936	0.0560724	intron-variant	FAM188A	GRCh38.p7	10:15845217	CATATTGATGGGATT[G/T]ATGGAAGTTTATTTT	80013
rs150939681	snp	G/T	0.00716266	0.059414	intron-variant	FAM188A	GRCh38.p7	10:15789584	AAATTACTTGATCTT[G/T]AAACAGTGTTACAGC	80013
rs150942325	snp	C/G	0.00835141	0.0640778	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15861212	GCTTAAAAAAAGAGG[C/G]CTTGTATTGCCCGAG	80013
rs150961038	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15850128	ACTGTGAAGATTTCA[C/T]GGACATTTATCACTT	80013
rs151002966	snp	G/T	0.00199481	0.0315187	intron-variant	FAM188A	GRCh38.p7	10:15804232	GAGGGTTGGCGGGGG[G/T]GCGGGGGATGGAAGT	80013
rs151011608	snp	G/T	0.00239393	0.0345281	intron-variant	FAM188A	GRCh38.p7	10:15816645	AAATCATGATAGATT[G/T]TGATTAAAAGATTCC	80013
rs151100888	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15829455	TTTCTCCTAGTTAAT[C/T]GTGATGTGCAGCCAA	80013
rs151144626	in-del	-/A	0.0383715	0.133092	intron-variant	FAM188A	GRCh38.p7	10:15818970	TGCTTTAAAATGGTG[-/A]AATCTCCTGGTATGT	80013
rs151153288	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15825711	TTGTATATATTTACC[A/G]TGTACAACATGTTTT	80013
rs151170610	snp	G/T	0.00597247	0.0543191	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15786062	ATTCAGGTTGGCCCA[G/T]ATGCCTCTGCTATTC	80013
rs151172541	snp	C/T	0.00676609	0.0577691	intron-variant	FAM188A	GRCh38.p7	10:15813648	GGCACATACTATAAT[C/T]CAGTAAAAAGCTCAT	80013
rs151194374	snp	G/T	0.0023933	0.0345097	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15783214	ACTCCAGGAGCACTT[G/T]CCCGGTGCTTGCTTC	80013
rs151207830	in-del	-/AAC	0.00314407	0.0395241	intron-variant	FAM188A	GRCh38.p7	10:15837160	GGAAAAACAGCACTG[-/AAC]AACATTAATCAAAGG	80013
rs151216907	snp	A/C/T	0.00239393	0.0345281	intron-variant	FAM188A	GRCh38.p7	10:15842701	CTTTGTAAACTGTCA[A/C/T]GTGGAATGCAAATTC	80013
rs151268497	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15832595	AAACTCTGACCTTTA[C/T]TAGAAATCACCAAAA	80013
rs151310900	snp	C/G	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15794696	GTAATATGAGAAATT[C/G]TCATTTTCCTTGGTA	80013
rs180784764	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15802526	CCCCATGACTCAATC[A/G]CCTCCCACCAGGTCC	80013
rs180801199	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15793473	GGCTCCTAAGATCCT[C/T]AAGATTCTGAAATGG	80013
rs180813069	snp	A/G	0.0023933	0.0345097	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15785748	TTAACAATCTTTTTT[A/G]ACAATTACATTCTGA	80013
rs180852962	snp	A/G	0.00438332	0.0466095	intron-variant	FAM188A	GRCh38.p7	10:15833310	TTTTAAGCAAAGAGT[A/G]CAGTAATATCTCTGA	80013
rs180870534	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15847581	TACTTAATAGGATCT[C/T]TGTGTTAAAGAAGTC	80013
rs180890240	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15818699	AAACAGAGATGAACA[A/C]TGAAAACACCATGCT	80013
rs180948355	snp	C/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15858688	ACCATTACTAGAACT[C/G]CCACCCTGAATCTTC	80013
rs181032620	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15849743	CCCATCTCCTCTCTT[A/T]ATCTTCAATCTCTTC	80013
rs181066207	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15847290	CAAGATTCCAAATCA[A/G]ATAAAGACATTCCGA	80013
rs181068091	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	FAM188A	GRCh38.p7	10:15862354	CTGATTACAATTTAC[A/G]TAATTCTTCCACTTC	80013
rs181075742	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15832707	TTTTAAACAGTAAAA[C/T]GGGTTGTACTGTGGT	80013
rs181088205	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15818238	GATTTCCATCACATC[A/G]CATGGTGCCTCGTGT	80013
rs181089347	snp	A/T	0.0023933	0.0345097	downstream-variant-500B	FAM188A	GRCh38.p7	10:15778101	CTGTGCTCTCAGGGT[A/T]ATTGGGTAGAAACAT	80013
rs181091575	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15801053	ATATCAAGGTAACAG[A/G]AGAAGCAGCTTCTGC	80013
rs181098957	snp	C/T	0.00199481	0.0315187	intron-variant, utr-variant-3-prime	FAM188A	GRCh38.p7	10:15785351	TTACCTAAAAAATTA[C/T]TACAAGTAACTGTCT	80013
rs181139232	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15824574	CCCAAATAGGTATAA[A/G]TGGATACTTCATATC	80013
rs181156879	snp	A/T	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15810489	AGCAAAAGCTAGTTT[A/T]TCTATTTGCCCTCCA	80013
rs181164911	snp	C/T			intron-variant	FAM188A	GRCh38.p7	10:15795171	CTGGGCAAGGTGCTT[C/T]CCACATTATTCATTT	80013
rs181211791	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15858097	GAACAAACAAATGAA[C/T]ACAACAGTTAACATA	80013
rs181218521	snp	A/C	0.00438332	0.0466095	intron-variant	FAM188A	GRCh38.p7	10:15844675	TTTAGAAAAGATTCA[A/C]AGAAACACAACTATT	80013
rs181220578	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15829132	GTAATAGAATGAAGC[C/T]GACTGAGGTAAAGCA	80013
rs181223287	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15815340	GCTTGAGAAAAGGCA[A/G]TTATGTATCTTGCTC	80013
rs181236567	snp	C/G	0.00517822	0.0506191	intron-variant	FAM188A	GRCh38.p7	10:15798752	GCCATTGCACTCCAG[C/G]CTGGGCAACAGGGCA	80013
rs181239213	snp	A/C	0.00315109	0.0395679	intron-variant, downstream-variant-500B	FAM188A	GRCh38.p7	10:15782251	ATAAAGGACTATTAA[A/C]ACTTTAAATTATATT	80013
rs181311303	snp	A/G	0.00795532	0.062565	intron-variant	FAM188A	GRCh38.p7	10:15849348	TGCCAGCAAATGGGC[A/G]GCAGGAAAGATGACA	80013
rs181321686	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15820927	CCAGCCTGGGCAACA[C/T]AGCAAGACCCTGTCT	80013
rs181409703	snp	A/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15835830	CATTTCTAAATATAC[A/T]CCTTTTGTTTTCCAT	80013
rs181435206	snp	C/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15789857	GTTTAAAAAAAACAG[C/G]CCTGAAATGAAGAGT	80013
rs181474431	snp	A/G	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15798365	ATTTTAGCCATAGAA[A/G]GTTTAGATCAGATTC	80013
rs181479690	snp	C/T	0.00159617	0.0282053	intron-variant	FAM188A	GRCh38.p7	10:15781888	GTTGATTTAGAAACA[C/T]GCTACACTGCCAAGG	80013
rs181559620	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15805400	TCTGGTGAACAGAGA[A/C]TAGTTATACTGGTAA	80013
rs181572898	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15850168	ATACTCTTATAATTT[A/C]CTATGCCTGTCTTTA	80013
rs181586325	snp	G/T	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15822061	AGAAGAAAAAGAGAC[G/T]CAATACCTATGTAAA	80013
rs181587950	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15836482	ACATAGTCCCTAGCA[C/T]AGAGTCAATCAACGC	80013
rs181627539	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15828398	AGAAAGTAGATGAGC[A/G]GATGCTAGGGCTGGC	80013
rs181708382	snp	A/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15857402	ACATGTGTAATTTAT[A/G]CTACGTTATATTTAC	80013
rs181719743	snp	A/C	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15790857	TGCTCAGTCTGTACA[A/C]CGTTTTTCAGGAGCA	80013
rs181722148	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15806194	GTATGTTGCTTGTGC[C/T]ACATGTACTCTATTT	80013
rs181736141	snp	A/G	0.00874735	0.0655527	intron-variant	FAM188A	GRCh38.p7	10:15814836	TAAAAAGAAGGGCCT[A/G]TTTCACTCTTGGGAA	80013
rs181810783	snp	C/G	0.000798403	0.0199641	intron-variant	FAM188A	GRCh38.p7	10:15836132	ATCTTCCACAGTTGC[C/G]TCTCTGGTGTCTTAT	80013
rs181821381	snp	A/G	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15821544	AAGGAAGAAGAGAGC[A/G]GTACTGAACCATAGT	80013
rs181829130	snp	C/T	0.000399281	0.0141238	intron-variant	FAM188A	GRCh38.p7	10:15805470	TTTCAAAGTTAGGAC[C/T]CTTTGTATCACTGGA	80013
rs181831359	snp	A/G			intron-variant	FAM188A	GRCh38.p7	10:15790334	AGACAGATTGGCCTT[A/G]ACTAAAAGGTTATGA	80013
rs181880850	snp	C/G	0.00119737	0.0244387	intron-variant	FAM188A	GRCh38.p7	10:15844351	TGAGAAGTGAGATGG[C/G]GATATTCATTATTTC	80013

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