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

BPTF

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs113068376	snp	A/G	0.000100015	0.00707089	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67893672	ACTGACTATCACCCA[A/G]TTAGAAAACAACATC	2186
rs113198035	snp	C/T	0	0	intron-variant	BPTF	GRCh38.p7	17:67917141	TTGTCCTTTTTTTTT[C/T]TTTTTTTTTGAGATA	2186
rs113212277	snp	G/T	0.5	0	intron-variant	BPTF	GRCh38.p7	17:67962785	GTTTTCTTCTTCATA[G/T]CATATTTTGACCATT	2186
rs113254959	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67882048	CCATGTTGGCCAGGC[C/T]GGTCTCGAACTCCTG	2186
rs113269773	snp	A/G	0.0402882	0.136092	intron-variant	BPTF	GRCh38.p7	17:67905415	TCTGTCTCAAAAAAA[A/G]AAAAATTCAGGCCAG	2186
rs113282660	snp	A/G	0.5	0	intron-variant	BPTF	GRCh38.p7	17:67859232	CTCACTGCAGCGTCA[A/G]TCTCCTAGGCTCAGG	2186
rs113310597	snp	A/G	0.0107246	0.0724382	intron-variant	BPTF	GRCh38.p7	17:67847021	TGTGGGTTTGTTGTT[A/G]TTTTTTTGTTTTATT	2186
rs113332041	snp	C/T	0.0310518	0.120672	intron-variant	BPTF	GRCh38.p7	17:67958676	GGGGAGGTTGGAGTG[C/T]GCTGAGATTGTGCCA	2186
rs113358259	snp	C/G	0.5	0	intron-variant	BPTF	GRCh38.p7	17:67879435	GTGAGCCACCGCGCC[C/G]GGCTAGGGCTGGTGT	2186
rs113361619	snp	C/T	0.0154538	0.0865337	intron-variant	BPTF	GRCh38.p7	17:67922732	TGCAGCAGAGACCAT[C/T]TGGCTATTTAAGAAG	2186
rs113374786	snp	C/T	0.5	0	intron-variant, missense	BPTF	GRCh38.p7	17:67946056	CTCTCTCAGATCCAG[C/T]CACAGGTTGTGGCTC	2186
rs113390426	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67957559	TTTTTAAAAAAATTT[C/T]TAAGTCAGATTTTAA	2186
rs113397466	snp	A/G	0.5	0	intron-variant	BPTF	GRCh38.p7	17:67847455	GGAGGCAGAGCTTGC[A/G]GTGAGCAGAGGTCGC	2186
rs113415407	snp	A/T	0.5	0	intron-variant	BPTF	GRCh38.p7	17:67962782	TTAGTTTTCTTCTTC[A/T]TATCATATTTTGACC	2186
rs113416437	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67852464	TCCCCTTGCCCTCCT[C/T]TTTATTTTTAGTTTA	2186
rs113425565	snp	G/T	0.5	0	intron-variant	BPTF	GRCh38.p7	17:67859502	CTAAATCTCAAAGAG[G/T]TTAAATAATTTGCCC	2186
rs113437066	in-del	-/TTT	0.493837	0.055168	intron-variant	BPTF	GRCh38.p7	17:67840105	ATGGAAAAATACTGA[-/TTT]TTTTTTTTTTTTTTG	2186
rs113439669	snp	C/G	0.0433465	0.140692	intron-variant	BPTF	GRCh38.p7	17:67846927	GCTGGTCCTAAACTC[C/G]GGACCTCAAGTGATC	2186
rs113452554	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67917862	TGTCGCCTAGGCTGG[A/T]ATGCAGTGGCCGGAT	2186
rs113460835	in-del	-/C	0.136506	0.222754	intron-variant	BPTF	GRCh38.p7	17:67915736	GCTCTGATCCTCATT[-/C]CCGAGCCAACTCAGA	2186
rs113461722	snp	C/T	0.5	0	intron-variant	BPTF	GRCh38.p7	17:67882971	CCACGCCACTGCACT[C/T]CAGCCTGGGTGATAG	2186
rs113471076	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67950055	TGAGACTGTCTCAAA[A/G]AAAAAAAAAAAAAAA	2186
rs113538212	snp	A/G	0.0414363	0.137845	intron-variant	BPTF	GRCh38.p7	17:67965467	CTGTGGGAGGCCAAG[A/G]CAGGAGGATCACTTG	2186
rs113544348	snp	C/T	0.00755907	0.0610114	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67896950	TAGAAAACAAATATA[C/T]CTTAGATCCCATTAT	2186
rs113558789	snp	A/G	0.0146672	0.084371	intron-variant	BPTF	GRCh38.p7	17:67974686	GCTTACCGGTTTCTC[A/G]AGGACACTGCAAAGG	2186
rs113594383	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67865875	GAAGTAAAGAAGAGG[A/G]ATGAGATATTATTTG	2186
rs113608508	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67953981	TTTTTTTTTTTTTTT[C/T]TTTTTTTTTTTTTTT	2186
rs113626817	snp	C/G	0.0441095	0.141807	intron-variant, utr-variant-3-prime	BPTF	GRCh38.p7	17:67981937	ATGCTTCTGTAAATG[C/G]CTCTATTTGTCCAGT	2186
rs113637912	snp	A/G	0.0115144	0.0749975	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67897425	CTTTTATTAGAACTT[A/G]GAATTTTAAAGCCTT	2186
rs113645217	snp	C/T	0.5	0	intron-variant	BPTF	GRCh38.p7	17:67859238	GCAGCGTCAGTCTCC[C/T]AGGCTCAGGCCATCC	2186
rs113663538	snp	A/T	0.121717	0.214577	intron-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67919218	TAATAATAATAATAA[A/T]AAAATATAATGCTTG	2186
rs113675407	snp	C/G	0.5	0	intron-variant	BPTF	GRCh38.p7	17:67947898	ATACTTGTTTATCTT[C/G]ATTGAAGTTCATTAA	2186
rs113722700	snp	A/G	0.040671	0.13668	intron-variant	BPTF	GRCh38.p7	17:67835555	TATTGCATTTCTGCA[A/G]TAAGATTTGGGGTCA	2186
rs113728219	snp	A/G	0.0402882	0.136092	intron-variant	BPTF	GRCh38.p7	17:67908914	ACCTCAGCTCACTGC[A/G]ACCTCCGCCTCCTGG	2186
rs113740934	snp	C/T	0.5	0	intron-variant	BPTF	GRCh38.p7	17:67961318	AACACTTTAGTATAC[C/T]AGGTTCATTCACTCC	2186
rs113765616	snp	A/T	0.5	0	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67898241	GTGTTGCATGCCTTT[A/T]GTCCCAGCTACTAGG	2186
rs113772550	snp	A/C	0.5	0	intron-variant	BPTF	GRCh38.p7	17:67950073	AAAAAAAAAAAAAAA[A/C]ATTTCATAACATATC	2186
rs113779703	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67829253	CTTGCCAGGCATTTT[C/T]CTTTATTGGCTGTGA	2186
rs113787521	snp	A/T	0.5	0	intron-variant	BPTF	GRCh38.p7	17:67976711	AAAAAAAAAAAAAAA[A/T]AAAATAAGAATAAAA	2186
rs113822774	snp	A/C/G/T	0.5	0	utr-variant-3-prime	BPTF	GRCh38.p7	17:67982579	AAAGAAAGCAAGAAA[A/C/G/T]AAAGATACTATGGGG	2186
rs113825738	snp	A/G	0.0479149	0.147179	intron-variant, utr-variant-5-prime	BPTF	GRCh38.p7	17:67889741	TGAACCCAGGAGGCA[A/G]AGGTTGCAGTGAGCC	2186
rs113846643	snp	A/G	0.00676609	0.0577691	intron-variant	BPTF	GRCh38.p7	17:67852243	TTTATTGATTTGAGT[A/G]TTAATATTTTTATAT	2186
rs113890698	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67962076	TGAGCCTGGGAGGTC[C/T]AGGCTGCAGGGGGCC	2186
rs113907307	snp	C/G/T	0.0577693	0.159994	intron-variant	BPTF	GRCh38.p7	17:67964728	GTTCTTGGCCGGGCA[C/G/T]GGTGGCTCATGCCTG	2186
rs113920001	snp	C/T	0.5	0	intron-variant	BPTF	GRCh38.p7	17:67961888	CCGAGTCAGGAGAAT[C/T]GCTTGAACCCGGGAG	2186
rs113943278	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67953980	TTTTTTTTTTTTTTT[C/T]TTTTTTTTTTTTTTT	2186
rs113950608	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67899172	ATTGCTGAAGCAATA[A/G]TGCAGGTAGACAAAT	2186
rs113956576	snp	A/C	0.22263	0.248497	intron-variant	BPTF	GRCh38.p7	17:67916405	GACCAGCCTGGCCAA[A/C]GTGGTGAAACCCCGT	2186
rs113966366	snp	A/G	0.0475351	0.146656	intron-variant	BPTF	GRCh38.p7	17:67895199	TTAGCTGGGTGTGGT[A/G]GCACATGCCTGTAGT	2186
rs113986508	snp	A/G	0.0562307	0.157967	intron-variant	BPTF	GRCh38.p7	17:67866807	CGTGCATTGCTTAAT[A/G]ATGGGGATACATTCT	2186
rs113995110	snp	C/T	0.0263992	0.111815	upstream-variant-2KB	BPTF	GRCh38.p7	17:67823714	GCATTTCTCTGGCAA[C/T]TAGTGCTTGTATTTT	2186
rs113996107	snp	A/G	0.0341408	0.126114	intron-variant	BPTF	GRCh38.p7	17:67839814	AGTAAATACCTAGGA[A/G]TATGATTTCTGGGTT	2186
rs114032784	snp	C/T	0.00993419	0.0697739	intron-variant	BPTF	GRCh38.p7	17:67890323	TACTTCTGATTTTGC[C/T]GTTTCATATTTTTCT	2186
rs114053795	snp	A/T	0.0275645	0.114116	intron-variant	BPTF	GRCh38.p7	17:67860509	TCTTATACATGAATT[A/T]ATAGTCCATCTGAGA	2186
rs114086141	snp	C/T	0.00953498	0.0683855	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911177	AGACTTCTACAAATT[C/T]TTCAAAAAATCTCTC	2186
rs114104779	snp	C/T	0.0232847	0.105357	intron-variant	BPTF	GRCh38.p7	17:67926162	ACAGGCATGCACCAC[C/T]GTGTCTGGCTGATTT	2186
rs114113687	snp	A/G	0.0379877	0.132479	intron-variant	BPTF	GRCh38.p7	17:67965057	TATGAAAAACAAAAA[A/G]GGGACTGGGCGTGGT	2186
rs114225277	snp	A/G	0.0182019	0.0936463	intron-variant	BPTF	GRCh38.p7	17:67943535	TTACTTGGTGTTTGC[A/G]TTACATATCTAAAAC	2186
rs114317140	snp	A/G	0.0333695	0.124785	intron-variant	BPTF	GRCh38.p7	17:67958218	CTGTGGTCCTAGCTA[A/G]GTACTTGGGAGGCTG	2186
rs114339338	snp	A/G	0.00517822	0.0506191	intron-variant	BPTF	GRCh38.p7	17:67870087	GAGCTTTAGGCCACA[A/G]TATGTTCTTAGAAAG	2186
rs114420488	snp	A/C	0.0325976	0.123435	intron-variant	BPTF	GRCh38.p7	17:67915252	CTGATTCTGTGCTTC[A/C]TTTTCACATTGAACT	2186
rs114438238	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67858676	ATTCAGCAGTTAGCA[C/G]GTCACGTTCACGCAG	2186
rs114455446	snp	C/T	0.00835141	0.0640778	intron-variant	BPTF	GRCh38.p7	17:67930752	AGTTCGAGAACCACC[C/T]AAACAAAATGGCAAA	2186
rs114475252	snp	C/T	0.0376037	0.131863	intron-variant	BPTF	GRCh38.p7	17:67960707	GCTTTAAAAACTGAT[C/T]ATTTAGAATCAATTA	2186
rs114480971	snp	C/T	0.0372196	0.131242	intron-variant	BPTF	GRCh38.p7	17:67924123	CCTGCCTCAGGCAGG[C/T]GGCCACCACCATGCC	2186
rs114482789	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67866910	AGGTTATACGGCATA[A/G]CCTGTTGCTGCTAGG	2186
rs114554545	snp	C/T	0.0123036	0.0774623	intron-variant	BPTF	GRCh38.p7	17:67954482	CAACAGGGAGCCGGC[C/T]CTTATCACTGCCTCA	2186
rs114560383	snp	A/G	0.0372196	0.131242	intron-variant	BPTF	GRCh38.p7	17:67970592	TACCTAAATGTGTTT[A/G]GAAATGCATAGAAAA	2186
rs114649548	snp	A/G	0.0146672	0.084371	intron-variant	BPTF	GRCh38.p7	17:67837743	CTTTTTCTAGAATCT[A/G]CTAAGGTTTACTCAG	2186
rs114653313	snp	A/G	0.00795532	0.062565	intron-variant	BPTF	GRCh38.p7	17:67828314	CGGTAATTGAAACAC[A/G]GAGACTGAATTGCAT	2186
rs114758094	snp	A/C	0.0372196	0.131242	intron-variant	BPTF	GRCh38.p7	17:67925800	TCTTGTGTATCTTTC[A/C]GTTTACTATAGGTCC	2186
rs114758885	snp	A/G	0.00716266	0.059414	intron-variant	BPTF	GRCh38.p7	17:67833103	CGCCCCGCCTGATTT[A/G]CCTCTTATGGACATT	2186
rs114854891	snp	A/G	0.0240643	0.107019	intron-variant	BPTF	GRCh38.p7	17:67959362	CTTCATTTTGTTTCT[A/G]GTTGTCTTAGTTGGG	2186
rs114859785	snp	A/G	0.00597247	0.0543191	intron-variant	BPTF	GRCh38.p7	17:67895663	ACACGGGGTCTCATT[A/G]TGTTGCCCAGGCTGT	2186
rs114868071	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67836142	AGTATGTCCTAGTGT[G/T]TCTGGGTTCTCCTGT	2186
rs114870514	snp	A/T	0.0123036	0.0774623	intron-variant	BPTF	GRCh38.p7	17:67878866	TACACTGAATTTTGA[A/T]TGTTAACCTAATCTC	2186
rs114875037	snp	A/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67828999	AATTATTGTTAGTAG[A/T]TAAGAACTTGTAATA	2186
rs114944673	snp	G/T	0.0372196	0.131242	intron-variant	BPTF	GRCh38.p7	17:67914049	ATGGAACATAAACAC[G/T]GAAAACATGAGAGTT	2186
rs114951587	snp	A/G	0.00835141	0.0640778	intron-variant	BPTF	GRCh38.p7	17:67941093	ATGGAGGTACAAAGT[A/G]TTAAGAATATCTGTA	2186
rs114956509	snp	A/T	0.0142736	0.0832652	intron-variant	BPTF	GRCh38.p7	17:67918452	TACAATGAAACATTC[A/T]CATTTTATAAACTTA	2186
rs115019287	snp	C/T	0.0414363	0.137845	intron-variant	BPTF	GRCh38.p7	17:67898565	TCCTCCCACCTTGAC[C/T]TCCCAAAGTGCTGGG	2186
rs115088408	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67855445	TTTTGGTTTTACCAT[A/T]TCTGTATGTAAAATG	2186
rs115133113	snp	A/G	0.0372196	0.131242	intron-variant	BPTF	GRCh38.p7	17:67925675	AGTAGATATATCTAT[A/G]TACAGTATTATTAAC	2186
rs115147254	snp	A/C	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67896668	TTAAAGGCAAGGGCT[A/C]TATGCTTGAAAGGTA	2186
rs115196631	snp	A/G	0.00517822	0.0506191	intron-variant	BPTF	GRCh38.p7	17:67845330	ATGGTTCTTGCTTGA[A/G]TCAGTTACACCTCTG	2186
rs115210018	snp	C/T	0.417196	0.185864	intron-variant	BPTF	GRCh38.p7	17:67884423	CCCTGGCCCCTCCCT[C/T]TTTTTTTTTTCTGAC	2186
rs115274960	snp	A/G	0.0333695	0.124785	intron-variant	BPTF	GRCh38.p7	17:67954436	GTTTTCTCTCCCAAA[A/G]CCCAGTGGAGCCCAG	2186
rs115402182	snp	C/T	0.0111196	0.0737302	intron-variant	BPTF	GRCh38.p7	17:67861041	ACTCCTGGACCTGTC[C/T]GCAAGGCAGGCACCT	2186
rs115406022	snp	C/T	0.0418186	0.138422	intron-variant	BPTF	GRCh38.p7	17:67904323	GCATGAGCCACTGCT[C/T]CTGGCCTACTTTTGA	2186
rs115466722	snp	C/T	0.0126979	0.078662	intron-variant	BPTF	GRCh38.p7	17:67934016	GCCATTGCACTCCAA[C/T]GTGGGCAACAAGAGT	2186
rs115475983	snp	C/T	0.0372196	0.131242	intron-variant	BPTF	GRCh38.p7	17:67903158	GGGCCCCTTTCTCTG[C/T]GGATGTAAGAAACCT	2186
rs115476567	snp	A/C	0.0103295	0.0711199	intron-variant	BPTF	GRCh38.p7	17:67922168	CAAACCACTGCAGTC[A/C]CCTAAAATCACTTCT	2186
rs115495912	snp	C/T	0.00517822	0.0506191	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67886817	TATGAATTGAATTCA[C/T]TTTTTTTTAAAGCTG	2186
rs115496390	snp	A/T	0.040671	0.13668	intron-variant	BPTF	GRCh38.p7	17:67835222	TCTCTTAAAAAAAAA[A/T]TTTAAGTAAAATGAA	2186
rs115531375	snp	C/T	0.0103295	0.0711199	intron-variant	BPTF	GRCh38.p7	17:67829093	TAAAAATTGGTCTAA[C/T]TGTTTTTTGTTTTTG	2186
rs115537506	snp	A/G	0.0310518	0.120672	intron-variant	BPTF	GRCh38.p7	17:67930857	CTGCTTGGGAGGGTA[A/G]GGGACGAGAATTGCT	2186
rs115589642	snp	C/T	0.0372196	0.131242	intron-variant	BPTF	GRCh38.p7	17:67898537	CTGATCTTGAATCTC[C/T]GACCTCAAGTTATCC	2186
rs115589920	snp	A/G	0.0107246	0.0724382	intron-variant	BPTF	GRCh38.p7	17:67873692	AAATGAACCCTATAC[A/G]GACACATAGGCATTC	2186
rs115604856	snp	C/T	0.00716266	0.059414	intron-variant	BPTF	GRCh38.p7	17:67942348	AGGACAAACCAACAT[C/T]ATGAGGAAAGAAGAA	2186
rs115618262	snp	G/T	0.0383715	0.133092	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67896583	CTACATACATTTATG[G/T]AGATTTTAAAAGCAT	2186
rs115709814	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67972490	CTCAGGTAATCCGTC[C/T]GCCTCTGCCTTCCAA	2186
rs115710386	snp	C/T	0.0221141	0.102801	intron-variant	BPTF	GRCh38.p7	17:67950364	TCTTCCAGTTAAAGT[C/T]AGAAACCAGAAACCC	2186
rs115712346	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67877201	GACCAAAATAGATAA[A/G]GTCTGGGCCCTTGGT	2186
rs115739185	snp	C/G	0.0271762	0.113356	upstream-variant-2KB	BPTF	GRCh38.p7	17:67823587	AAAATATGGGCACCT[C/G]CATTGGCCTAGGTCT	2186
rs115773188	snp	C/T	0.0154538	0.0865337	intron-variant	BPTF	GRCh38.p7	17:67934239	AATAAAAGACATGAC[C/T]GGGCGCTGTGGCTCA	2186
rs115780161	snp	C/T	0.0232847	0.105357	intron-variant	BPTF	GRCh38.p7	17:67955011	TTTAAAAGCTTTGGC[C/T]GGGTACGGTGGCTCA	2186
rs115951095	snp	A/C	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67967857	AAATAAGTAGCCATC[A/C]ATAGAGGAGTAGCTA	2186
rs116115857	snp	A/T	0.0349115	0.127424	intron-variant	BPTF	GRCh38.p7	17:67957549	TCTAAAAGAATTTTT[A/T]AAAAAATTTTTAAGT	2186
rs116120133	snp	A/G	0.00636936	0.0560724	intron-variant	BPTF	GRCh38.p7	17:67922334	GAGGAGATTTTATCT[A/G]TTCTTAGGTTTCACA	2186
rs116121495	snp	G/T	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67833906	GAATCCTTAGTGATA[G/T]ATTGGTTAGGCTGGG	2186
rs116153493	snp	A/G	0.0654984	0.168698	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67896641	TTTAGGGATATAGAC[A/G]TTTGTAAAATTTTAA	2186
rs116209696	snp	A/G	0.00716266	0.059414	intron-variant	BPTF	GRCh38.p7	17:67957343	TTATTTTCCTGAGAG[A/G]CTATAAATCATGATG	2186
rs116233719	snp	A/G	0.0228947	0.104514	intron-variant	BPTF	GRCh38.p7	17:67878767	TCATTTTCTATAAAT[A/G]TTCTGTTTTTTGCTT	2186
rs116261084	snp	C/T	0.0372196	0.131242	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67897587	CAGAAAGGGACCCAC[C/T]GAGCTCCTTTTGGGT	2186
rs116269658	snp	A/C	0.0337553	0.125452	intron-variant	BPTF	GRCh38.p7	17:67921569	TAAAAAGATAATGTC[A/C]TTAGATAGAAACGTA	2186
rs116279095	snp	A/G	0.0329836	0.124112	intron-variant	BPTF	GRCh38.p7	17:67875228	TATAATGTTATATTC[A/G]TGTCTCTATTTATAC	2186
rs116354860	snp	G/T	0.00755907	0.0610114	downstream-variant-500B	BPTF	GRCh38.p7	17:67984444	ATAGCTGTTAGCCTT[G/T]CCAAATTGTACAAAA	2186
rs116432297	snp	G/T	0.0310518	0.120672	intron-variant	BPTF	GRCh38.p7	17:67972459	TGGTTGACCAGGCTG[G/T]TCTCGAACTCTTGAC	2186
rs116435616	snp	A/G	0.0115144	0.0749975	intron-variant	BPTF	GRCh38.p7	17:67856022	ATTTTCAATCTGGCA[A/G]TTACGTTCTTTGATT	2186
rs116518528	snp	C/G	0.0341408	0.126114	intron-variant	BPTF	GRCh38.p7	17:67915523	GTACAGCGCATTCTG[C/G]CTTCTGCCTTTTTCT	2186
rs116631790	snp	A/G	0.0372196	0.131242	intron-variant	BPTF	GRCh38.p7	17:67935344	AGGCAGGAGGATCAC[A/G]TGGGCCCAAGAGGTC	2186
rs116771041	snp	C/G	0.0372196	0.131242	intron-variant	BPTF	GRCh38.p7	17:67923414	TAGCTTGACTTTACT[C/G]CACCTTTGATTTTAA	2186
rs116783323	snp	A/G	0.00496626	0.0495829	missense, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67886257	CTGCTAAGGCAGCTG[A/G]TGATCCTGAAAATGG	2186
rs116830162	snp	A/C	0.0111196	0.0737302	intron-variant	BPTF	GRCh38.p7	17:67976177	TAAAGTCTTTTTTTG[A/C]AAATTCAAGAAGTGG	2186
rs116833071	snp	A/G	0.00636936	0.0560724	intron-variant	BPTF	GRCh38.p7	17:67906393	TATAAATAAGCTATT[A/G]ATTGAGTTTTTACAA	2186
rs117019286	snp	A/G	0.095934	0.196885	intron-variant	BPTF	GRCh38.p7	17:67917573	AGAATGTTTTTGTCC[A/G]TTTGGAAAGGTCTTA	2186
rs117037971	snp	A/T	0.0193772	0.0965046	utr-variant-3-prime	BPTF	GRCh38.p7	17:67983024	TCTGCACCAGGCTAA[A/T]ATGAGTAAAATCTAT	2186
rs117060605	snp	A/C	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67941710	CTCACTCTACATAAA[A/C]TCAATTCCAGGAGGA	2186
rs117069581	snp	A/T	0.0134861	0.0810011	intron-variant	BPTF	GRCh38.p7	17:67958359	CAGAGTACAGTAAAG[A/T]AGCTGGCCAAAACCA	2186
rs117079868	snp	C/T	0.0107246	0.0724382	intron-variant	BPTF	GRCh38.p7	17:67970873	ATAAACAACATGCCA[C/T]TGGACATCTTTGTTT	2186
rs117099749	snp	C/T	0.0142736	0.0832652	intron-variant	BPTF	GRCh38.p7	17:67865237	ATTAAGGGAACTCCA[C/T]CCATATCCTTTTATT	2186
rs117134135	snp	A/C	0.00279162	0.0372561	intron-variant	BPTF	GRCh38.p7	17:67844655	ATCTGCCCATCTCGG[A/C]CTCCCAAAGTACTAG	2186
rs117138629	snp	C/T	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67894397	GCAGTGGTGTAGTCT[C/T]GGCTTGCTGTAACCT	2186
rs117163533	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67887397	CTACTTTTAGCTCTT[C/T]GTTGTCATACAGACA	2186
rs117167493	snp	A/C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67960275	AATCCTGGAAACCAG[A/C/T]TGAACATGAATGGTC	2186
rs117234918	snp	C/T	0.0916144	0.193427	intron-variant	BPTF	GRCh38.p7	17:67883110	CACAGATCAGGAGTT[C/T]GAGACCAGCCTGGCC	2186
rs117235289	snp	G/T	0.077417	0.180873	intron-variant	BPTF	GRCh38.p7	17:67843179	ATATAGATACATATA[G/T]ATATCTACATACATC	2186
rs117263029	snp	C/G	0.00279162	0.0372561	intron-variant	BPTF	GRCh38.p7	17:67968076	CACGAGTAATCGTAT[C/G]AACACGAATGGCTAC	2186
rs117295490	snp	A/C	0.0248432	0.108648	intron-variant	BPTF	GRCh38.p7	17:67830042	TATCGCTGAATAATG[A/C]TTTAATTCATTTTTA	2186
rs117301874	snp	A/G	0.0189856	0.0955633	intron-variant	BPTF	GRCh38.p7	17:67943944	CCATTGGGGGAGCTT[A/G]AACTGGAACTCTGGA	2186
rs117307545	snp	A/G	0.0547245	0.156101	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67897525	GACCAAGATGGTGGA[A/G]TAAAAGTCCCCAACT	2186
rs117311772	snp	C/G	0.00835141	0.0640778	intron-variant	BPTF	GRCh38.p7	17:67857751	GGATTATAGGCGTGA[C/G]CCACTGCGTCTAGAC	2186
rs117391632	snp	C/G	0.0170251	0.090679	intron-variant	BPTF	GRCh38.p7	17:67936425	TACTTAGAAAACTGA[C/G]AGTTGTGGTAAATTG	2186
rs117415449	snp	A/G	0.005742	0.0532731	intron-variant	BPTF	GRCh38.p7	17:67886118	AAAATCAGATATTCT[A/G]TTTTTCTAGAAGAAC	2186
rs117447672	snp	A/G	3.3042e-05	0.00406447	intron-variant	BPTF	GRCh38.p7	17:67920146	GAAACACCAAAAGGT[A/G]AGAAATAGAATTCTA	2186
rs117505826	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67887125	TTTCCTTATTCTCTC[A/G]CTTAAATTCAACAAC	2186
rs117522913	snp	C/T	0.00358779	0.0422022	intron-variant	BPTF	GRCh38.p7	17:67913662	TTGCATGATAAACAT[C/T]TGTTTTGGAGTTCTC	2186
rs117652432	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	BPTF	GRCh38.p7	17:67984296	TGTTTTTAACAAATT[A/G]TGGCAAATTCTAAAC	2186
rs117691887	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67941043	AAGAGGTTTTGTTTT[C/T]AGTGAAACTTCACAA	2186
rs117695516	snp	A/T	0.0248432	0.108648	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67897676	ACACTCTTAGGCAGG[A/T]AAAGGATTTCTGGTT	2186
rs117715138	snp	A/G	0.00914312	0.0669923	intron-variant	BPTF	GRCh38.p7	17:67969505	TTTTGGTGTGTTCTT[A/G]TATGCATGGGTGTTA	2186
rs117725031	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67936452	ATTGCCAGAGAAACT[A/G]TAAATGCTGGTATTA	2186
rs117743191	snp	C/T	0.0130921	0.0798413	intron-variant	BPTF	GRCh38.p7	17:67838476	GTGTAAACATGTGTA[C/T]GTACATACTTTTTTT	2186
rs117751660	snp	C/T	0.0134861	0.0810011	intron-variant	BPTF	GRCh38.p7	17:67861434	CCTCTTGGATTCAAG[C/T]GACTCCCGAGTGGGT	2186
rs117759125	snp	A/T	0.095934	0.196885	intron-variant	BPTF	GRCh38.p7	17:67957300	AAAAAATAAAAAAAT[A/T]AAAAAAATAAAGGAA	2186
rs117784881	snp	A/G	0.0115144	0.0749975	intron-variant	BPTF	GRCh38.p7	17:67971759	CAGTGAGCCAAGATC[A/G]TTGCGTTGCAGTGAT	2186
rs117820910	snp	C/G	0.00953873	0.0683987	intron-variant	BPTF	GRCh38.p7	17:67843356	AGGCTGGAGTGCAGT[C/G]GTGTGATGTCGGCTC	2186
rs117840547	snp	C/T	0.0023933	0.0345097	intron-variant	BPTF	GRCh38.p7	17:67866873	GAACATCATAGAGTA[C/T]ACTTACACAAACCAT	2186
rs117861826	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67913356	TCAAAATTGGCCAAC[G/T]AATGTACTAAAGTTT	2186
rs117867933	snp	G/T	0.0107246	0.0724382	intron-variant	BPTF	GRCh38.p7	17:67968073	AGCCACGAGTAATCG[G/T]ATCAACACGAATGGC	2186
rs117878400	snp	A/G	0.0166325	0.0896639	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67887343	TTATGTATTGTTGCT[A/G]TTAATCTTCAATTTT	2186
rs117937325	snp	A/G	0.0894459	0.191631	intron-variant	BPTF	GRCh38.p7	17:67832699	AAAGAAGCCCGCACC[A/G]TCAGCATCACTCCCT	2186
rs117959886	snp	A/G	0.0165278	0.0893908	intron-variant	BPTF	GRCh38.p7	17:67916279	TCTTTCACAGTGTTC[A/G]TTTTTCCAACTGAAT	2186
rs118033764	snp	A/G	0.0170251	0.090679	intron-variant	BPTF	GRCh38.p7	17:67956457	CAAGTAGCTGGCACT[A/G]TAGGCATGTGCCACC	2186
rs118059219	snp	C/T	0.00318978	0.0398085	upstream-variant-2KB	BPTF	GRCh38.p7	17:67823991	CTTTTGTATTTTTAG[C/T]ACAGAACTTTTGCAT	2186
rs118066372	snp	C/G	0.0119091	0.0762411	intron-variant	BPTF	GRCh38.p7	17:67850851	CATATTAAATGCTCT[C/G]CATTGTTCTGTGTGG	2186
rs118105213	snp	A/G	0.0894459	0.191631	intron-variant, utr-variant-5-prime	BPTF	GRCh38.p7	17:67888714	TAAACATAGTAGAGG[A/G]TGTTCTTTAATAAAA	2186
rs118161511	snp	C/T	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67962011	AGCCGGGCCTGGTGG[C/T]GCATGCCTATAGCCC	2186
rs118168221	snp	A/G/T	0.025256	0.109658	intron-variant	BPTF	GRCh38.p7	17:67856925	TTGAAGGGGAGAATG[A/G/T]TGGTTTAGGAATCTG	2186
rs137859641	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67958031	GTATGGCAAATGCAT[A/G]TTGAGGAAGTAGTAT	2186
rs137895315	snp	C/T	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67954027	GGCCTTGTTCTGTTG[C/T]CCAGGCGGGAGTGCA	2186
rs137934373	snp	A/G	0.0341408	0.126114	intron-variant	BPTF	GRCh38.p7	17:67851084	CCAGACTGGGAAGCA[A/G]CAGCCTGGGCTCCAG	2186
rs137937430	snp	A/G	0.00151717	0.0275006	synonymous-codon, nc-transcript-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67918801	ATGGGATGATATGGC[A/G]GCCAAGGCTCCTCCA	2186
rs137975299	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67878006	TTGATGGATGTTTAC[G/T]AAGTTAACACATCTG	2186
rs137997719	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	BPTF	GRCh38.p7	17:67982859	GAAAGGAGCTGCTAT[A/G]TACACATGTGCACAC	2186
rs138011827	in-del	-/TTA			intron-variant	BPTF	GRCh38.p7	17:67853595	CACAAATGCAGTTAT[-/TTA]TTATTATTATTATTA	2186
rs138066789	snp	A/G	0.00517822	0.0506191	intron-variant	BPTF	GRCh38.p7	17:67953096	CTTCCCGAGTAGCTG[A/G]GACTACAGGCGCAGG	2186
rs138069789	snp	A/T	0.00352762	0.0418493	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67912039	GCTAAAAAATACCAC[A/T]GACAAAAAGAATAAT	2186
rs138075212	snp	C/T	0.00914312	0.0669923	intron-variant	BPTF	GRCh38.p7	17:67871561	TATCCTATGCCTGTA[C/T]GGTAATTATGAAATG	2186
rs138088856	snp	C/G	0.0178098	0.0926698	intron-variant	BPTF	GRCh38.p7	17:67839260	TGCGAATATTTCATG[C/G]TTAACTGTGGGTTTG	2186
rs138101065	snp	A/G	0.00279162	0.0372561	intron-variant	BPTF	GRCh38.p7	17:67978915	GGCACGGTGGCTCAT[A/G]CCTGTAATCCCAACA	2186
rs138131969	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67948494	CTTTTATAACTAAAT[A/G]TGTAGTTATATTGTA	2186
rs138151997	snp	A/G	0.00478085	0.0486577	intron-variant	BPTF	GRCh38.p7	17:67935640	AACTGTAGATCACCT[A/G]AGGTCAGGAGTTCAA	2186
rs138173873	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67935151	AAACAAGACCTGATG[C/T]GGTGGCTCACACCTG	2186
rs138179486	in-del	-/GGAT			intron-variant	BPTF	GRCh38.p7	17:67873993	GATGGATGGATGGAT[-/GGAT]ATGTGTCAAAAGGAC	2186
rs138188947	snp	C/T	1.65187e-05	0.00287386	synonymous-codon	BPTF	GRCh38.p7	17:67948174	GAAGCGTGAAGAGAG[C/T]GTGGAGCAGAAACGT	2186
rs138205467	snp	C/G	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67899687	AGGCGTGTGCCACCA[C/G]GACCAGCTAATTTTT	2186
rs138207871	snp	C/T	0.000692053	0.0185889	missense	BPTF	GRCh38.p7	17:67940553	GCTTAACTTCAGCAA[C/T]GTCCACTTCAAATAT	2186
rs138230804	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67931550	CTGATCTTCCTGTTA[C/T]ATTCTGTGGGTTACA	2186
rs138233313	snp	A/T	0.00358779	0.0422022	intron-variant	BPTF	GRCh38.p7	17:67976996	GAATAAAAGAAACTC[A/T]TAGATAAAACCGACA	2186
rs138257113	snp	G/T	0.00438332	0.0466095	intron-variant	BPTF	GRCh38.p7	17:67863295	CTTTTCTTTTTCTTT[G/T]CATTTTTTTGAGACA	2186
rs138283648	snp	A/G	0.0119091	0.0762411	intron-variant	BPTF	GRCh38.p7	17:67879852	TCACCCCCAACACCC[A/G]ACCCGAGAGCATTAA	2186
rs138297396	snp	A/C/T	0.00158238	0.0280869	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67866676	ACAAATCCTTTCTGG[A/C/T]GGCAGCTAATGGTGA	2186
rs138327324	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67830841	AGGGATTGGGCTGGA[C/T]TGTGATCCTCAGCCC	2186
rs138334328	snp	A/G	4.96767e-05	0.00498356	synonymous-codon	BPTF	GRCh38.p7	17:67959717	AGGCCTTCTGTCCAC[A/G]CCCACCTTACCTGCT	2186
rs138351274	snp	A/G	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67852185	TAGTATAATGACGTT[A/G]TATTTATACAAGACT	2186
rs138387052	snp	C/T	0.0912534	0.193131	intron-variant	BPTF	GRCh38.p7	17:67969840	CTGAGGCAGGAGAAT[C/T]GCTTGAACCCAGGAG	2186
rs138432836	snp	A/G	0.000153988	0.00877328	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67911985	TCAGCAGAAGAAATT[A/G]GAGGAGAGACCAGTT	2186
rs138440188	snp	A/G	0.00358779	0.0422022	intron-variant	BPTF	GRCh38.p7	17:67890550	GGGACAGTCACTGTG[A/G]CCAGCTAGTGGTGTG	2186
rs138469313	snp	C/G	0.00993419	0.0697739	intron-variant	BPTF	GRCh38.p7	17:67882016	ATTTTTGTATTTTTA[C/G]TAGAGACAGGATTTC	2186
rs138485442	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67925705	CATAGTTATACATAA[C/T]TATTTAAAAATCATA	2186
rs138533941	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67914176	TTCCCCTTAGGCTTC[A/G]TTTTTGTGTGTCTTT	2186
rs138551195	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67881733	GTCTTGAACTTCTGA[C/T]CTTGTGATCTGCCCA	2186
rs138556852	snp	C/T	0.0475351	0.146656	intron-variant	BPTF	GRCh38.p7	17:67953524	CAGCCTCCCAAAGTG[C/T]TAGGATTACAGGCGT	2186
rs138599625	snp	C/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67856237	TCTTGGTCGTCCAAC[C/G]CTGTTATCCAGTTTT	2186
rs138632854	snp	C/T	0.0107246	0.0724382	intron-variant	BPTF	GRCh38.p7	17:67839065	CATCTGATTTTCTTA[C/T]ATTTGTATCTCCTTT	2186
rs138636027	snp	A/G	0.000153988	0.00877328	synonymous-codon, nc-transcript-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67918816	GGCCAAGGCTCCTCC[A/G]GGAGGAGGGACTACA	2186
rs138674521	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67947528	AGGTAATGTCAAGTG[C/T]TTAGCCTAGCACGGT	2186
rs138687561	snp	A/C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67836165	TCTCCTGTATAAAAC[A/C/G]TCTTAGGAGTCACTG	2186
rs138694415	snp	G/T	0.089084	0.191327	intron-variant	BPTF	GRCh38.p7	17:67872614	GGGAGGCTGAGGTGT[G/T]AGAATCGCTTGAACC	2186
rs138729570	snp	C/T	0.000114666	0.00757098	intron-variant	BPTF	GRCh38.p7	17:67940424	AGCATTCATAATGTT[C/T]TGCTGTTTGGGTAGG	2186
rs138733747	snp	A/G	0.00597247	0.0543191	intron-variant	BPTF	GRCh38.p7	17:67967892	AGATGGTGTCTGAGT[A/G]GAGTATTATGCAGCT	2186
rs138752015	snp	A/G	0.00517822	0.0506191	intron-variant	BPTF	GRCh38.p7	17:67864321	TGCTTGAGGCCAGAC[A/G]TTCAAGACTAGCCTG	2186
rs138759618	snp	C/T	0.00517822	0.0506191	intron-variant	BPTF	GRCh38.p7	17:67977841	AGAGGGAGATTCCAT[C/T]TCAAAAAAAAAAAGT	2186
rs138775783	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67971809	CTTCAGCCTGGGCAA[C/T]AGAGTGAGACTCCAT	2186
rs138779341	snp	A/G/T	0.000516125	0.0160562	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67912666	CACGATGACCTCCAC[A/G/T]GTGGCCACAGAATCA	2186
rs138779477	snp	A/T	0.00755907	0.0610114	intron-variant	BPTF	GRCh38.p7	17:67872427	ATGTAGTTGTGTTTG[A/T]AAATGGCCGGGCGTG	2186
rs138786985	snp	C/T	0.0115144	0.0749975	intron-variant	BPTF	GRCh38.p7	17:67900304	GAGATGGGGTTTTGT[C/T]GTGTTGGCCAGGCTG	2186
rs138850009	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67979679	TTGGGAAATGGTTAA[C/G]TGAGCTTGGTTCTCC	2186
rs138855849	snp	A/G	0.00953873	0.0683987	intron-variant	BPTF	GRCh38.p7	17:67867185	AATTAGGGATGCTAT[A/G]CATTTTAGTGTTTTA	2186
rs138868196	snp	A/G	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67922355	AGGTTTCACATCTCC[A/G]CTTTATATTGGTAAC	2186
rs138875240	snp	A/G	0.00716266	0.059414	intron-variant	BPTF	GRCh38.p7	17:67829543	CTGGAATGAGTAACA[A/G]TGCATGACAGTGAGT	2186
rs138981392	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67885635	TACCTTTCAGTTAAT[C/T]TGGGCATAGTATTCA	2186
rs138990442	in-del	-/G			intron-variant	BPTF	GRCh38.p7	17:67905602	GGTCCCAGCTACTTG[-/G]GGGGTCTGAGGCAGG	2186
rs139007859	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67849529	TCTGGAATTTCATCT[A/G]ATGTGTATTAATTTT	2186
rs139012703	snp	A/G	0.0872718	0.189788	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67896456	CTCTACGGGTAATGA[A/G]TAACTAGAAACTGTC	2186
rs139051091	snp	C/T	0.0372196	0.131242	intron-variant	BPTF	GRCh38.p7	17:67907101	GATGAGGGAGGATCG[C/T]TTGAGCCCAGGAGTT	2186
rs139064570	snp	A/G	0.00716266	0.059414	intron-variant	BPTF	GRCh38.p7	17:67844483	CGATCTCCTGACCTC[A/G]TGATCCGCCCGCCTT	2186
rs139121177	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67864826	TTGTTTATTTTTGAG[A/G]CAGAGTCTCGCTCTG	2186
rs139127370	snp	A/G	0.00557542	0.0525036	intron-variant	BPTF	GRCh38.p7	17:67894539	TTCACTGTGTTGGCT[A/G]GGCTGGTCTTGAACT	2186
rs139147700	snp	A/C	0.0130921	0.0798413	intron-variant	BPTF	GRCh38.p7	17:67972343	CGGGTTCAACCGATT[A/C]TTCCACCTCAGCCTC	2186
rs139156737	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67902433	CTGTCAGGTTATCCA[C/T]CGTATTGTGCCTACA	2186
rs139171539	snp	A/G	0.00279162	0.0372561	intron-variant	BPTF	GRCh38.p7	17:67962290	GGTAGAACTAAGAGT[A/G]CCAATGGTATCAGCA	2186
rs139200231	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67966287	GCAATGCCAGCATCA[C/G]TCAGTGACGGCTCAT	2186
rs139214014	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67857248	CTTACTGCAAGCTCC[A/G]CCTCCCGGGTTCACA	2186
rs139217597	snp	A/C	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67919777	TTGAGTATTGCCACC[A/C]GGAGCTCAGCTATAC	2186
rs139217919	snp	G/T	0.0314385	0.121371	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67896373	AAGTTTACAATAGAA[G/T]GAAAACATTTGGAGA	2186
rs139228790	snp	C/T	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67895537	CGCCATCACAGCTCA[C/T]TGCAGCCTTGACCTC	2186
rs139231512	snp	C/T	0.00223253	0.0333359	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911528	GAAATGATTTTTTCA[C/T]CGATGACTCTAAACT	2186
rs139262955	snp	G/T	0.00517822	0.0506191	intron-variant	BPTF	GRCh38.p7	17:67893118	ATACATGAAAGCAGT[G/T]AATAATAGTATCTGA	2186
rs139265808	snp	C/T	0.0103295	0.0711199	intron-variant	BPTF	GRCh38.p7	17:67964585	AGCTTTACCATATCC[C/T]CACACCACGTCAGCT	2186
rs139294277	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67932849	AAATAAAGGCCATAA[A/G]AAGAAAGAAAAGACA	2186
rs139312760	snp	A/G	0.000134766	0.00820762	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67910901	AGCTCTTAGATTCTG[A/G]CAGTGATAAACCCTG	2186
rs139322063	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67882953	CAGTCAACTGAGATC[A/G]CGCCACGCCACTGCA	2186
rs139325513	snp	C/T	0.0111196	0.0737302	intron-variant	BPTF	GRCh38.p7	17:67955548	TGTAGCTTCAGAGGC[C/T]GGGCACGGTGGCTCA	2186
rs139329704	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67927222	ACCTCTCTAGTCTCC[A/G]TTTCCTCATCTTATA	2186
rs139353057	snp	A/G	0.000217834	0.0104341	missense, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67875588	GATAAAGGTAACTCT[A/G]TGTCAGCAAATCTTG	2186
rs139357086	in-del	-/C			intron-variant	BPTF	GRCh38.p7	17:67879136	TGTTGTTAATTATTT[-/C]TTTTTTTTTTTTTTT	2186
rs139367506	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67845261	TGTAAGGTGATTCTT[G/T]GAGAATATCCTATTG	2186
rs139384287	snp	G/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67832224	GGTTTTTTAAAATGA[G/T]AAGCCTCAGGAGGCA	2186
rs139387934	snp	C/T	0.000148843	0.0086255	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911362	CATACCACAAACAAA[C/T]TTTATCCAAAAGATC	2186
rs139422646	snp	C/T	1.64817e-05	0.00287064	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67893531	TGCTTTGAATAAGCA[C/T]CAGCACAGAGAAGAC	2186
rs139428019	snp	A/G	0.0236746	0.106192	intron-variant	BPTF	GRCh38.p7	17:67949436	AAAAATTAGCTGGGC[A/G]TGGTGGCAGGCACCT	2186
rs139446109	snp	A/C	0.0134861	0.0810011	intron-variant	BPTF	GRCh38.p7	17:67936946	CAAGTCCAGATATTC[A/C]TTTATTCATTCAACA	2186
rs139450820	snp	C/T	0.0539704	0.155153	upstream-variant-2KB	BPTF	GRCh38.p7	17:67824205	GCAATCACGGCTCAC[C/T]GCAACATCCACCTCC	2186
rs139456089	snp	C/T	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67933550	CTCCAGCCTGGGAGA[C/T]GGAGCACGACCTGTT	2186
rs139461023	snp	G/T	0.0236746	0.106192	intron-variant	BPTF	GRCh38.p7	17:67977952	CCCCACCTCCCGGAT[G/T]CAAGTGGTTCTCTTG	2186
rs139472191	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67874151	TATAATTAATATCCA[C/T]GAGTGCGTACTGATA	2186
rs139474918	snp	C/G	0.00874735	0.0655527	intron-variant	BPTF	GRCh38.p7	17:67943576	TTACAGTTTAGCACA[C/G]ACACACCCCATAGGT	2186
rs139486844	snp	A/G	0.0437281	0.141251	upstream-variant-2KB	BPTF	GRCh38.p7	17:67823952	TAGCTGGGACTACAG[A/G]CACGCACCACCACGC	2186
rs139543011	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67836757	TTTTTGTAGACAGCA[A/G]AATTATTTCACACAC	2186
rs139553934	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67832762	GCCACTAATCTACTT[C/T]GATTCCCTGTTGATT	2186
rs139579386	snp	A/G	0.00636936	0.0560724	intron-variant	BPTF	GRCh38.p7	17:67936470	AATGCTGGTATTACT[A/G]TGGATACACAGAGCC	2186
rs139581841	snp	C/T	0.000153988	0.00877328	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67854212	TTGAAAGCAGTTCTG[C/T]GTGAAGAAGACACTT	2186
rs139590110	snp	C/G	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67942729	GAACAACTCAGGTGT[C/G]TATCAAAATCAGTTA	2186
rs139591786	snp	C/T	0.000433984	0.0147243	synonymous-codon, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67891992	CCAGCAGGTGGCAGC[C/T]GCTGCACATGAAGCA	2186
rs139607948	snp	A/C/G	0.00716904	0.0595202	intron-variant	BPTF	GRCh38.p7	17:67834939	CTAGGCAGGCCAAGC[A/C/G]TGGTGGCTCATACCT	2186
rs139609750	snp	A/G	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67872839	GCACTGCTAACGCCT[A/G]TAACCCCAGTGCTTT	2186
rs139647949	in-del	-/T	0.0115144	0.0749975	intron-variant	BPTF	GRCh38.p7	17:67869298	GAAAAAACAAAAAAA[-/T]ATTTTCTGTGTGTTA	2186
rs139655166	snp	G/T	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67875155	AGAGATCAGGATACC[G/T]TCCCCTCTTATAACG	2186
rs139668259	snp	C/T	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67859593	TGTTTTATAAGAATA[C/T]TTTCAATACCTTATT	2186
rs139709271	in-del	-/CCTCCAGCC/CCTCCAGCCCCTCCAGCC/CCTCCAGCCCCTCCAGCCCCTCCAGCC	0.340257	0.242501	cds-indel	BPTF	GRCh38.p7	17:67959642	CCAGTGACACCAGCT[lengthTooLong]CCTCCAGCCCCTCCA	2186
rs139719058	snp	C/T	0.00517822	0.0506191	intron-variant	BPTF	GRCh38.p7	17:67910620	GCCTGGCCAACATTG[C/T]GAAACCCTGTCTCTA	2186
rs139739479	snp	A/G	0.00914312	0.0669923	downstream-variant-500B	BPTF	GRCh38.p7	17:67984786	GGCATGCGCCACCAC[A/G]CCTGGCTAATTTTGT	2186
rs139746979	snp	C/G/T	1.66626e-05	0.00288635	missense, utr-variant-3-prime	BPTF	GRCh38.p7	17:67982269	CTCATAACAACAAAC[C/G/T]GCAGTCTACAGCTTC	2186
rs139756948	snp	A/T	0.000482581	0.015526	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67912747	CACAGAAAATTGTGC[A/T]AAATCCACTGTCACA	2186
rs139767484	snp	C/G	3.62555e-05	0.00425752	missense	BPTF	GRCh38.p7	17:67945588	GCTCAGCCTGAAGTT[C/G]AGACTCAGCCTGAAG	2186
rs139786693	in-del	-/TTG	0.423257	0.180228	intron-variant	BPTF	GRCh38.p7	17:67829113	TTTTGTTTTTGTTTT[-/TTG]TTGTTGTTGTTTTTT	2186
rs139860861	snp	C/T	0.00398564	0.0444627	intron-variant	BPTF	GRCh38.p7	17:67918225	ACAGGCGTGAGCCAC[C/T]GCATCTGACCTCATT	2186
rs139898036	snp	A/G	0.00478085	0.0486577	intron-variant	BPTF	GRCh38.p7	17:67879583	TGTAAAGGAGTATCT[A/G]AGGCTGGTGGTTTAT	2186
rs139898499	snp	C/T	0.00597247	0.0543191	intron-variant	BPTF	GRCh38.p7	17:67857712	GCTCGAGCCATCTGC[C/T]CTTCTCGGCCTCTCA	2186
rs139915626	snp	C/T	0.0182019	0.0936463	intron-variant	BPTF	GRCh38.p7	17:67923513	TTTGAAGCAGAGTCT[C/T]GCTCTGTCAGCTAGG	2186
rs139951561	snp	C/T	1.6492e-05	0.00287154	synonymous-codon	BPTF	GRCh38.p7	17:67944312	TTCCTCTTTACCCCA[C/T]TGGCAACAACAGCCA	2186
rs139987934	snp	C/T	0.0111196	0.0737302	intron-variant	BPTF	GRCh38.p7	17:67926393	GCAGTGGCGCGATCT[C/T]GGCTTACTGCAAGCT	2186
rs139997334	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67859999	TTTTTCTTAGTGGAA[C/T]AGTAAAATACTTATG	2186
rs140006505	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67922542	TGCTCCAGGTGGAAG[A/G]AACAGGTTGTATAAA	2186
rs140025994	snp	G/T	0.00517822	0.0506191	intron-variant	BPTF	GRCh38.p7	17:67980881	AAACAAATTAGGCTG[G/T]GTGCAATGGTGCATG	2186
rs140059870	in-del	-/TATA			intron-variant	BPTF	GRCh38.p7	17:67880948	AGGGTGTATGTATAT[-/TATA]TATATATACACACAC	2186
rs140091815	in-del	-/A	0.00795532	0.062565	intron-variant	BPTF	GRCh38.p7	17:67957524	CTAGCCTACATGGTG[-/A]AACCCTGTCTCTAAA	2186
rs140104673	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67842235	TAGACATATATCTAC[A/T]TACATTGACAGATAT	2186
rs140123908	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67954747	CAAAGTGTGTGCCCA[C/G]TATACAATCTTGGTT	2186
rs140129929	snp	C/T	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67950608	TTTGGGAGGCTGAGG[C/T]GAGCGGATCATTTGA	2186
rs140153147	snp	C/T	0.0023933	0.0345097	intron-variant	BPTF	GRCh38.p7	17:67974570	GTGGTTTTACCTGCA[C/T]GTCTGACCATCTGGC	2186
rs140194546	snp	C/T	0.000630517	0.0177443	intron-variant	BPTF	GRCh38.p7	17:67909808	GGGGTGATAAGAATG[C/T]ACTGGATCAGGGTCC	2186
rs140201830	snp	A/G	0.00279162	0.0372561	intron-variant	BPTF	GRCh38.p7	17:67844640	TCCTGAGCTCAGGCA[A/G]TCTGCCCATCTCGGC	2186
rs140208584	snp	C/T	4.94287e-05	0.00497111	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67928499	GGAACCAAAATGGTA[C/T]TAACTACTAAAGTTG	2186
rs140226714	snp	C/T	0.089084	0.191327	intron-variant	BPTF	GRCh38.p7	17:67858014	GCTGGTCTCGAACTC[C/T]TGACCTTGTGATCCG	2186
rs140234292	snp	C/T	0.0372196	0.131242	intron-variant	BPTF	GRCh38.p7	17:67921133	GAGAATTGCTTGAGC[C/T]TGGGAAGTGGAGGTT	2186
rs140256698	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67902894	TTCTTCTGCCACTAG[C/T]GCTCTTAGAGACAAG	2186
rs140283792	snp	A/T	1.64738e-05	0.00286995	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67918757	GCTGGAGTGAGCCTG[A/T]TGTTACGGTTACTGT	2186
rs140290217	snp	C/T	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67974209	ATTTTATTTCAAACA[C/T]GTCGTTCTCCTAGGA	2186
rs140304426	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67970383	AGCCTAGGCAACAAG[C/T]GAGACCTTGTCCCAC	2186
rs140305267	snp	C/T	0.0103295	0.0711199	intron-variant	BPTF	GRCh38.p7	17:67913254	ATCTCACAAGAATAT[C/T]TCATTTTTAAAAAAT	2186
rs140307173	snp	G/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67924227	CCCAAAATGATGGGA[G/T]TACAGGCATGAGCCA	2186
rs140353318	snp	A/C	0.00795532	0.062565	intron-variant, utr-variant-5-prime	BPTF	GRCh38.p7	17:67888870	GGTTGCTGGGGACTT[A/C]TATAGGATTAAACAA	2186
rs140366569	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67913355	TTCAAAATTGGCCAA[C/G]TAATGTACTAAAGTT	2186
rs140380622	snp	A/C	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67977087	AGATTATGGAAGAAT[A/C]AATCTAAAAGTTTAA	2186
rs140417869	snp	G/T	0.00279162	0.0372561	intron-variant	BPTF	GRCh38.p7	17:67855165	ACTTAGCCAGGTGTG[G/T]TGGCGCACACCTGTA	2186
rs140449569	snp	C/T	0.0158469	0.0875917	intron-variant	BPTF	GRCh38.p7	17:67906600	CCCTTTTCTGTGATT[C/T]TTCTCTTACCTCACC	2186
rs140450037	snp	C/T	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67947292	CACTGTCTGTCTATC[C/T]GCTAATCTTTGTATA	2186
rs140456884	snp	A/G	0.00358779	0.0422022	intron-variant	BPTF	GRCh38.p7	17:67876604	TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGACCA	2186
rs140490508	snp	A/G/T	0.00755907	0.0610114	intron-variant	BPTF	GRCh38.p7	17:67976211	GGCATAGTGGCTCAC[A/G/T]CCTGTAATCCCAACA	2186
rs140504721	snp	G/T	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67906075	ATGAGGTTTTTTTTG[G/T]GGGGAGGGGTTGTTT	2186
rs140546512	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67899274	AAGTACAGAGCCAGC[C/T]GCTTTGGATGCTTGG	2186
rs140552977	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67938092	CCTGGGCAATAGAGC[A/G]AGACTTCACAGACCC	2186
rs140573996	snp	C/G	0.0134861	0.0810011	intron-variant	BPTF	GRCh38.p7	17:67960673	CCATACTTTTTACAG[C/G]ACCAAAAAGTCTGAT	2186
rs140581229	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67869825	CGTCTCTACTAAAAA[A/T]ACAAAAAAAAAAAAA	2186
rs140629327	snp	G/T	1.65329e-05	0.0028751	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67866540	CTTGCAGAATTAATT[G/T]ACTGTCTAGACAAAG	2186
rs140673996	snp	A/C/G	1.65078e-05	0.00287291	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911900	GTGAGTTGGTTTCTG[A/C/G]TGAGTCCACTGGAAA	2186
rs140674433	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67870734	TGATGACTTTGACTT[A/G]ATGTTAACCTCTCAA	2186
rs140674820	snp	A/G	0.0256215	0.110247	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67888388	GGTCAGGAGTTCGAG[A/G]CCAGTCTGGCCAACA	2186
rs140702557	snp	A/G	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67928026	GTAGTTAGAATTACA[A/G]GCATGAGCCAGAATG	2186
rs140704870	snp	C/G	0.0119091	0.0762411	intron-variant	BPTF	GRCh38.p7	17:67960156	CCCTCTGAATTAACT[C/G]CAAATCAGTGAGTAA	2186
rs140709882	snp	A/G	0.089084	0.191327	intron-variant	BPTF	GRCh38.p7	17:67879181	GAGTTTCAGTCTTTC[A/G]CCCAGGCTGGAGTAC	2186
rs140728424	in-del	-/T	0.0402882	0.136092	intron-variant	BPTF	GRCh38.p7	17:67832210	TGCTTTTGGTTTTTT[-/T]AAAATGATAAGCCTC	2186
rs140794750	snp	C/T	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67893170	GTGTTAGTTTTCTTT[C/T]TGCAGGCATATCTTG	2186
rs140797399	snp	C/T	0.00438332	0.0466095	intron-variant	BPTF	GRCh38.p7	17:67853067	CTTGAACTTGAGAGG[C/T]GGAGGTCGCAGTGAG	2186
rs140810889	in-del	-/TTTT	0.0524604	0.153226	intron-variant	BPTF	GRCh38.p7	17:67881492	TTTTTTTTTTTTTTT[-/TTTT]GAGAGACAGAGTCTC	2186
rs140833245	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67881648	AGCCAGGACTATAGA[C/T]GCGCGCCACCACATC	2186
rs140867751	snp	C/T	0.030665	0.119967	intron-variant	BPTF	GRCh38.p7	17:67891771	TACACCAGATACGAG[C/T]TTTGGTGAAATAAGG	2186
rs140867963	snp	A/G	0.0023933	0.0345097	utr-variant-3-prime	BPTF	GRCh38.p7	17:67982519	TCAGATGGTTTTACT[A/G]TTGTGGCAGAAGCGA	2186
rs140900888	snp	A/G	3.29516e-05	0.00405891	missense	BPTF	GRCh38.p7	17:67945697	TTGCAGCACAGTCTC[A/G]GCCTCAAAGTAATGT	2186
rs140912226	snp	C/T	0.0948562	0.196037	intron-variant	BPTF	GRCh38.p7	17:67907448	GCAACCTCCACCTCC[C/T]GGGTTCAATCAATTC	2186
rs140912776	in-del	-/A	0.417359	0.185718	intron-variant	BPTF	GRCh38.p7	17:67883457	CATTTACATTATTAT[-/A]AATTGAAAACTATGT	2186
rs140930153	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67871266	GATCAACATGGCAAA[A/G]CCTCGTCTTTACTAA	2186
rs140938466	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67908145	ATAATCCTTCATACA[C/T]GAGTTTTCTTTCATT	2186
rs140941889	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67851193	TAACGAGTTGTTTGG[C/T]ATGAGGTCCAGTCAC	2186
rs140942173	snp	A/G	0.000577267	0.0169794	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67929440	ACAGCAACAGTCACA[A/G]TTAGGCCCAATACCT	2186
rs140944015	snp	A/G			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67896356	TCGAGATTGAATCTC[A/G]TAAGTTTACAATAGA	2186
rs141019552	snp	C/T	0.000153988	0.00877328	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67909726	CAGACCAAAATGAAA[C/T]GGATATCTCAAAGAT	2186
rs141033721	snp	C/T	0.0142736	0.0832652	intron-variant	BPTF	GRCh38.p7	17:67856083	TCCCTCTTGTATTTA[C/T]CTTGAGCTATGATTT	2186
rs141039309	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67866183	CATCATATTGTTACA[C/T]TGATGATCTTAAAGT	2186
rs141043312	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67933875	ACCAGCCTGGCCAAC[A/G]TGGTGAAACCCCATC	2186
rs141049517	snp	A/G	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67974864	TGGGTTTTTAGGAAA[A/G]CTTCATTACGTAGGC	2186
rs141082284	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67826821	AATTAAGGATTTGGA[C/T]AGATTGTGGTACACA	2186
rs141150029	snp	A/G	0.00636936	0.0560724	intron-variant	BPTF	GRCh38.p7	17:67865921	AAACCAGAACTTAGC[A/G]AAGCATTTACACCAT	2186
rs141167344	snp	C/T	6.58892e-05	0.00573936	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67854499	GATACAGTATGATGA[C/T]CATTGTAGGGTTTGT	2186
rs141172973	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67949312	AGAGGTTGCAGTGAG[C/T]CTTGATCGCACCACT	2186
rs141195114	snp	A/G	0.0341408	0.126114	intron-variant	BPTF	GRCh38.p7	17:67939689	AAGACCATCCTGACT[A/G]ACATGGTGAAACCCC	2186
rs141238002	snp	A/T	0.00302516	0.0387741	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911331	TTCCTCAGTTCTTAG[A/T]ATGAGTGATCCTAGT	2186
rs141244918	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67901840	CGTCAGCATTTTCAG[C/T]GCAAGAACTTTTGGA	2186
rs141269840	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67848405	GGCATGAGTAATTGC[C/G]TGTAATATAATTGTG	2186
rs141279814	snp	C/T	0.0205511	0.0992634	intron-variant	BPTF	GRCh38.p7	17:67946758	TTCTAGCCACACCTT[C/T]GTAAAAAAGTTTTTG	2186
rs141279903	snp	C/G	0.0111196	0.0737302	intron-variant	BPTF	GRCh38.p7	17:67899688	GGCGTGTGCCACCAC[C/G]ACCAGCTAATTTTTG	2186
rs141282624	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67941813	AAACAGATAGAAAAT[A/G]CTAACCATAAATGAA	2186
rs141311583	snp	A/T	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67836122	AAACTGAATTGCGAG[A/T]TGTTAGTATGTCCTA	2186
rs141331058	in-del	-/TTG			intron-variant	BPTF	GRCh38.p7	17:67840459	TTGCTGCTGCTCCTC[-/TTG]TTGTTGTTGTTGCTG	2186
rs141357727	snp	C/G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67838480	AAACATGTGTATGTA[C/G/T]ATACTTTTTTTTTTG	2186
rs141404296	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67931382	GGAGGCTGAGGCAGG[A/G]GGATTGCTTAAGCCC	2186
rs141405500	snp	A/G	0.00279162	0.0372561	intron-variant	BPTF	GRCh38.p7	17:67952714	ATTATTATTATTAAC[A/G]AAAGTCCATAGTTTA	2186
rs141476565	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67880891	TTGTTTTGTGGCCCA[A/G]CATTTAATTAATGTT	2186
rs141542626	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67917075	ACACAATGTTTAGAA[A/G]CAAACATGAACACAG	2186
rs141547581	snp	A/G	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67915809	CACAGACAGATTCTA[A/G]TTTACCTCTGTGTCC	2186
rs141552059	snp	A/G	0.00358779	0.0422022	utr-variant-3-prime	BPTF	GRCh38.p7	17:67983766	CTACCAACTTCTGGA[A/G]TTTATCTAATTATTG	2186
rs141557931	snp	C/T	0.00279162	0.0372561	intron-variant	BPTF	GRCh38.p7	17:67850599	GTCCGGAACTCCTGA[C/T]CTCGTGATCTGCCCA	2186
rs141562306	snp	C/T	0.0111196	0.0737302	intron-variant	BPTF	GRCh38.p7	17:67961699	AAAAAATTGGCCAGG[C/T]GTGGTGGCTAATGCC	2186
rs141618676	snp	C/T	0.0126979	0.078662	intron-variant	BPTF	GRCh38.p7	17:67873132	ACAAACCCAAAAATC[C/T]AAGAGGAGTACTGTG	2186
rs141654889	snp	A/G	0.0205511	0.0992634	intron-variant	BPTF	GRCh38.p7	17:67980067	AAACCTACCCAGGCC[A/G]GGTGTGGTGGCTTAT	2186
rs141658141	in-del	-/AATAATAATAAT			intron-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67919174	GAGACTCTGTCTCAA[-/AATAATAATAAT]AATAATAATAATAAT	2186
rs141698801	snp	C/T	1.65422e-05	0.0028759	missense, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67886299	CTCATACACCTGTCT[C/T]TATTCAGGAAGAGAT	2186
rs141710319	snp	C/T	0.00261958	0.0360961	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67912807	CACACCCTCCACAGG[C/T]GGCAGTGTGGACATC	2186
rs141726964	snp	A/G	0.0023933	0.0345097	intron-variant	BPTF	GRCh38.p7	17:67935703	TCTACTAAAAATGCA[A/G]AAATTAACTGGGAAT	2186
rs141727791	snp	A/G	0.0376037	0.131863	intron-variant	BPTF	GRCh38.p7	17:67925449	CAGGAGGATCCCTTG[A/G]GTCCAGGGGTTTGAG	2186
rs141727833	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67970758	AACTTAATACTTTTT[C/T]ACATCAGCTGTTATA	2186
rs141731229	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67971810	TTCAGCCTGGGCAAT[A/G]GAGTGAGACTCCATC	2186
rs141732741	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67869616	AGTTGGTTTCCTTCT[C/T]ATATTTTTTGCATTT	2186
rs141757726	snp	A/G	0.00557542	0.0525036	intron-variant	BPTF	GRCh38.p7	17:67977388	GGCATAATGGTGCAC[A/G]CCTGTAGTCTCAGCT	2186
rs141766501	in-del	-/T	0.0119091	0.0762411	intron-variant	BPTF	GRCh38.p7	17:67837504	CCTCCACCTCCTTGG[-/T]CCAAGCAGTTCCCCT	2186
rs141791037	snp	G/T	0.078151	0.181571	intron-variant	BPTF	GRCh38.p7	17:67967228	ATCACTACAACCTCC[G/T]CCTCCCAGGTTCAAG	2186
rs141798356	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67968861	GTGGCACATGCCTAT[A/G]ATCCTAGCTGCTCGG	2186
rs141806029	snp	C/T	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67832310	AAGATCGAAGGTGAC[C/T]GTATAGAAATAATTA	2186
rs141818046	snp	A/G	7.02654e-05	0.00592687	intron-variant	BPTF	GRCh38.p7	17:67928331	ACTATTTTGATTCAT[A/G]TTTCCTCTCCTTCAC	2186
rs141823022	snp	A/C	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67932120	AGAAATATAATTTTA[A/C]TTAGTACTTCAAAGC	2186
rs141831686	snp	A/G	0.0236746	0.106192	intron-variant	BPTF	GRCh38.p7	17:67967626	AGGAGTTCGAGACCA[A/G]CCTGGCCAACATGGC	2186
rs141844439	snp	C/G/T	3.30864e-05	0.00406723	missense	BPTF	GRCh38.p7	17:67959736	ACCTTACCTGCTGCT[C/G/T]CCCAGAAGAGGAAGC	2186
rs141857472	snp	A/G	3.29766e-05	0.00406045	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911818	ATTGTTCAGAATAGC[A/G]ATGAAAGCATTTCTG	2186
rs141869271	snp	A/G	9.3799e-05	0.00684768	intron-variant	BPTF	GRCh38.p7	17:67959534	TATTGTCTTTAATTG[A/G]TAACAGGAAGAGCTG	2186
rs141871726	in-del	-/AG	0.0955749	0.196603	intron-variant	BPTF	GRCh38.p7	17:67900534	CAGGAGTTCAAGACC[-/AG]CCTGGGCAACATAGG	2186
rs141874439	snp	A/C/T	0.00835141	0.0640778	intron-variant	BPTF	GRCh38.p7	17:67859046	ATTGAGCACTTCATG[A/C/T]GTGCCTCACAGTGTC	2186
rs141887973	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67862671	CTATAACAAAGTACT[A/G]TACCAAAAAAAAGTA	2186
rs141897566	snp	A/C/G	8.25533e-05	0.00642426	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67910964	TGAAAACAGAGTCAC[A/C/G]TGTAAATTGTCAGGA	2186
rs141918292	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67862442	ATGTACCGTCACCCT[A/G]TTTTTCAGATGGAGA	2186
rs141956010	snp	C/G	0.00835141	0.0640778	intron-variant	BPTF	GRCh38.p7	17:67864023	TGTGCCCAGTGGTAA[C/G]TTCAGGGAAGCCTGG	2186
rs141956418	in-del	-/C	0.192401	0.243274	intron-variant	BPTF	GRCh38.p7	17:67844062	AGCCACCGTGCCCGG[-/C]CCCCCGCCTTTTTTT	2186
rs141964612	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67900738	AAGAATACTGCACAC[A/G]GTAGCTCACGCCTGT	2186
rs141966768	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67859651	TCTTGAGAAATCTGC[A/C]ACTTGCATCGTTTTA	2186
rs141982305	snp	A/C	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67922154	CACAGCCTTTGATGC[A/C]AACCACTGCAGTCCC	2186
rs141983644	snp	C/T	0.00517822	0.0506191	intron-variant	BPTF	GRCh38.p7	17:67898653	AGATAAATACGAGTA[C/T]ATGAAGTCTTTTTTT	2186
rs142025347	snp	C/T	0.0123036	0.0774623	intron-variant	BPTF	GRCh38.p7	17:67857246	GGCTTACTGCAAGCT[C/T]CGCCTCCCGGGTTCA	2186
rs142088771	snp	A/G	0.00358779	0.0422022	intron-variant	BPTF	GRCh38.p7	17:67896049	GCTCACTGCAGCTCC[A/G]CCTCCCGGGTTCACG	2186
rs142120670	snp	C/G	0.0372196	0.131242	intron-variant	BPTF	GRCh38.p7	17:67933205	GGAGGTTGCAGTGAG[C/G]CGAGATTGTGCCACT	2186
rs142167831	snp	A/T	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67908332	ACTGGCTAATTTTTG[A/T]ATTTTTAGTAGAGAT	2186
rs142172548	in-del	-/CC/GG			intron-variant	BPTF	GRCh38.p7	17:67843176	ATATATAGATACATA[-/CC/GG]TAGATATCTACATAC	2186
rs142176119	in-del	-/AA			intron-variant	BPTF	GRCh38.p7	17:67952055	TGAGACTCTGTCTCA[-/AA]AAAAAAAAAAAAAAA	2186
rs142178290	snp	C/T	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67953106	AGCTGGGACTACAGG[C/T]GCAGGCTGCAACGCC	2186
rs142191632	snp	A/C	0.00517822	0.0506191	intron-variant	BPTF	GRCh38.p7	17:67955141	AAAAAAAATACAAAA[A/C]TTAGCCAGGCATGGT	2186
rs142197981	snp	A/G	0.00636936	0.0560724	intron-variant	BPTF	GRCh38.p7	17:67962415	GTGTAAGCGTTTGTT[A/G]CATTTACTTTTCCTT	2186
rs142206218	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67892692	ATACTTCTTTTTGAC[C/T]CTGACCCTCAGTCAC	2186
rs142220103	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67914191	GTTTTTGTGTGTCTT[C/T]TAATATTTTTCCAAT	2186
rs142245973	snp	C/T	0.000230616	0.0107357	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67854352	TAAGGAGTACCATCA[C/T]GTTCTTCCTTACCAA	2186
rs142293143	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67888447	CAAAAAATACTAGCC[A/G]GGCATGGTGGTGTGT	2186
rs142300680	snp	A/C/G	0.000734631	0.0191516	missense	BPTF	GRCh38.p7	17:67959628	GCTGCACCCTGCCCC[A/C/G]CAGTGACACCAGCTC	2186
rs142300955	snp	A/G	0.0123036	0.0774623	intron-variant	BPTF	GRCh38.p7	17:67847471	GTGAGCAGAGGTCGC[A/G]CCACTGCACTCCAGC	2186
rs142307832	snp	C/T	0.00143635	0.0267603	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912176	TTTCTGAGAGTAGAG[C/T]AGTAAGTGGTAATGT	2186
rs142321939	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67846428	CCAATAGAACTTTTT[A/G]TGATGATGGAAATAT	2186
rs142341573	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67849021	TGGTTAAGCTTCAGC[C/T]TCCCTTTGCATCAAT	2186
rs142354241	snp	C/T	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67885267	CTATACTCTTAGTGA[C/T]ACTATTAAATTGTCC	2186
rs142355841	snp	A/G	0.0901694	0.192235	intron-variant	BPTF	GRCh38.p7	17:67844588	GTATTTTTACTAGAG[A/G]CAGAGTTTCACCATG	2186
rs142389403	in-del	-/A			intron-variant	BPTF	GRCh38.p7	17:67879132	GGGCTGTTGTTAATT[-/A]TTTCTTTTTTTTTTT	2186
rs142392071	snp	A/G	0.0119091	0.0762411	intron-variant	BPTF	GRCh38.p7	17:67958439	TTTTAAAAAATATAT[A/G]AAAAGGGGCCAGGCA	2186
rs142397324	snp	A/G	0.0111196	0.0737302	intron-variant	BPTF	GRCh38.p7	17:67870518	ACCACTGTTACCTTT[A/G]TTTGTTCTCTCTGGT	2186
rs142404782	snp	A/T	1.65244e-05	0.00287436	missense	BPTF	GRCh38.p7	17:67945484	CCCTGCCACCAGCTC[A/T]GTCATCAAGTGTGGG	2186
rs142420752	snp	C/T	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67978592	GTGAGCCACCGTGCC[C/T]GGCCAGAAATTTTTG	2186
rs142425913	snp	G/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67882537	TATCCTAATGTGCAT[G/T]AATAATAAGAGGAAG	2186
rs142465983	snp	C/T	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67937591	TGAGGAAAGAGTCTT[C/T]TATGAAAAAGAAACA	2186
rs142509775	snp	C/G	0.095934	0.196885	intron-variant	BPTF	GRCh38.p7	17:67905341	TAAACCCAGGAGGCA[C/G]AGGTTGCAGTGAACC	2186
rs142531732	snp	C/G/T	6.59015e-05	0.00573995	missense, nc-transcript-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67918808	GATATGGCGGCCAAG[C/G/T]CTCCTCCAGGAGGAG	2186
rs142541600	snp	C/G	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67927396	AGAATATCTTTAATA[C/G]CTGTAGTTTTAAAGA	2186
rs142549398	snp	C/T	0.0130921	0.0798413	intron-variant	BPTF	GRCh38.p7	17:67930283	TGCTCACTGCAAACT[C/T]CACCTCCTGGGTTCA	2186
rs142551706	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67901946	TTACAGCTATGGCTG[G/T]GATAGCAAAACACCA	2186
rs142570105	snp	A/G	0.00569559	0.0530599	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67912153	GAAAGGTGAATGCTT[A/G]AAAGAAATTTCTGAG	2186
rs142619062	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67968044	CATTTCCCAGAAAAA[A/G]AAATGGTAATAGGAG	2186
rs142633440	in-del	-/TTTTTTTTTT	0.421526	0.181876	intron-variant	BPTF	GRCh38.p7	17:67835664	CCACAGTCCTGGTAA[-/TTTTTTTTTT]TTTTTTTTTTGAGAC	2186
rs142646584	snp	A/G	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67923245	ATTTTTTGTACAGAG[A/G]TGGGGTTTTGCTATG	2186
rs142682518	snp	A/G	6.62811e-05	0.0057564	missense, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67875606	TCAGCAAATCTTGGC[A/G]ACAACACAACAAATG	2186
rs142686231	snp	C/T	0.0111196	0.0737302	intron-variant	BPTF	GRCh38.p7	17:67906991	GAGTTCAAGAAACAG[C/T]CTGGGCAACATGGCA	2186
rs142703799	snp	A/G	0.000351762	0.0132573	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67826328	CATAGTACCTACAGC[A/G]GCACTCCAGGTACCC	2186
rs142726031	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67979744	ACAAGAAATAGCAGT[A/G]TAAGAAATTACCCTG	2186
rs142759459	snp	C/G	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67977926	ATGGCGCGATCTCGG[C/G]TCACCACAAGCCCCA	2186
rs142805142	snp	A/G	2.14383e-05	0.00327394	intron-variant	BPTF	GRCh38.p7	17:67854791	GTCTTAATTTTTTGT[A/G]TGCATTTAAAATTAG	2186
rs142806061	snp	A/G	0.0744748	0.178019	intron-variant	BPTF	GRCh38.p7	17:67935379	CTGCAGTGAGCCACA[A/G]TCTTGCCACTGCACC	2186
rs142824149	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67952196	TAAAAATAAATTTTA[A/G]TTTTATAAGATATGT	2186
rs142929496	snp	C/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67839102	TCAAATTACATTGCC[C/G]TCTACCATTGATGGG	2186
rs142960950	snp	A/G	4.9507e-05	0.00497504	synonymous-codon	BPTF	GRCh38.p7	17:67940632	GCTCACCATGGCTCA[A/G]CTTACTCAGTTAACA	2186
rs142982955	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67904467	TATAAAACTGTAAAA[G/T]TGTGTTACATTTTAC	2186
rs143010036	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67954241	GCCATGTTGCCCAGG[C/T]TGGTCTCAGAATCCT	2186
rs143010768	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	BPTF	GRCh38.p7	17:67983459	CACAGCTACTTATAT[C/T]TTATGAAGGGCATTT	2186
rs143012679	snp	A/G	0.000181271	0.00951855	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67922904	AAAGAGACCAGAAAC[A/G]CCCAAGCAAACTGGC	2186
rs143014087	snp	G/T	0.00013214	0.00812726	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912957	CAAAGTGAAACTGAT[G/T]AAATTTTCAAGACCA	2186
rs143042207	snp	A/G	0.0618563	0.164627	intron-variant, utr-variant-5-prime	BPTF	GRCh38.p7	17:67889674	TTAGCTGGGCATGGT[A/G]GCGGGCGCCTGTAAT	2186
rs143059429	snp	C/T	0.0372196	0.131242	intron-variant	BPTF	GRCh38.p7	17:67917988	GGCTAATTTTTTGTA[C/T]TTTTAGTAGAGATGG	2186
rs143121996	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67848280	CTGCATCTCTGCCCT[C/T]GGCAGGTAGTTTTGT	2186
rs143125472	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67962314	ATCAGCAAGGCCAGT[A/C]TGGTTCCCTGTGATT	2186
rs143149398	snp	G/T	0.00398564	0.0444627	intron-variant	BPTF	GRCh38.p7	17:67957338	CTAATTTATTTTCCT[G/T]AGAGACTATAAATCA	2186
rs143185448	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67941146	GCCCTATATATGATA[A/G]CTTGATATCAAAACT	2186
rs143213329	snp	A/C	0.00597247	0.0543191	intron-variant	BPTF	GRCh38.p7	17:67857272	GTTCACACCATTCTC[A/C]TGCCTCAACCTCCGA	2186
rs143229255	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67876221	GTATTTTGACATAAA[A/C]ATGTAAGTTGACCAG	2186
rs143253397	snp	A/G	0.00557542	0.0525036	intron-variant	BPTF	GRCh38.p7	17:67922534	TGGAATAGTGCTCCA[A/G]GTGGAAGAAACAGGT	2186
rs143269216	snp	C/T	0.00795532	0.062565	intron-variant	BPTF	GRCh38.p7	17:67863383	TCCACCTCCCAGGTT[C/T]AAGTGATTCTCCTGC	2186
rs143277517	in-del	-/A	0.0379877	0.132479	intron-variant	BPTF	GRCh38.p7	17:67974902	ATTACATCATTGGCC[-/A]TTGGTGATCAGCTTA	2186
rs143291809	snp	A/G	0.0379877	0.132479	intron-variant	BPTF	GRCh38.p7	17:67971497	TTAAAAAAAAAAAAA[A/G]AGAGTTATTTTTAAA	2186
rs143295184	snp	A/G	0.00517822	0.0506191	intron-variant	BPTF	GRCh38.p7	17:67964096	GAAAGTATTAAAACC[A/G]TAATACTAAAACTAT	2186
rs143356860	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67860883	ATTTTAAAAATCTGT[A/G]TTCATTTTCCGAATC	2186
rs143373843	snp	A/C	0.000153988	0.00877328	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67875003	CAGATGATGACCCTG[A/C]GCAAGGAAAATCTGA	2186
rs143388421	snp	A/G	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67924834	AGATCACAGCTCACC[A/G]AGCCTCGACATCCCT	2186
rs143406091	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67943282	AAAGCAAGAGTAAAT[A/G]AGTTTTGAGGGATTC	2186
rs143423003	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67857746	TGCTGGGATTATAGG[C/T]GTGAGCCACTGCGTC	2186
rs143430992	snp	A/G	0.0111196	0.0737302	intron-variant	BPTF	GRCh38.p7	17:67923624	AGCTGGGATTACGGG[A/G]GTGTGCCACCATGCC	2186
rs143471822	snp	A/G	0.00438332	0.0466095	intron-variant	BPTF	GRCh38.p7	17:67856651	TTGAGGTCTGTCCTC[A/G]AGAGTAAGCTCTAGA	2186
rs143493135	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67949115	TCATGCCCATAATCC[C/T]AACACTTTGGGAAGC	2186
rs143495041	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67902736	TGGGGAGTTTTTTGT[C/G]GGGGGAAAGGAGATA	2186
rs143544248	in-del	-/A			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67897037	ACCAATATCAAGAAT[-/A]AAAAAAGAGGCCGGG	2186
rs143564727	snp	A/G	0.00597247	0.0543191	intron-variant	BPTF	GRCh38.p7	17:67916444	AATATACAAAAATGA[A/G]CCCGGCGTGGTGGCG	2186
rs143571344	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67851008	GCAAATTGTAATGGA[A/T]AGAGGAGAAGGGAAA	2186
rs143607275	snp	C/T	0.00517822	0.0506191	intron-variant	BPTF	GRCh38.p7	17:67977235	AGTGTGTGCTATTGG[C/T]CAGGCATGGTGGCTC	2186
rs143634514	snp	A/G	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67839832	TGATTTCTGGGTTGT[A/G]TGTTTATGAGAAACT	2186
rs143640536	snp	C/T	0.00636936	0.0560724	intron-variant	BPTF	GRCh38.p7	17:67906377	ACCACTGCGCCTGGC[C/T]TATAAATAAGCTATT	2186
rs143649750	snp	A/G	0.00438332	0.0466095	intron-variant	BPTF	GRCh38.p7	17:67950781	AGAGCAGAGGTTGCA[A/G]TGAACTAAGATCATG	2186
rs143688675	snp	A/G			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67896447	CAGTGTTTACTCTAC[A/G]GGTAATGAGTAACTA	2186
rs143716685	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67946960	TATAGCTTGCTTCGC[C/T]CAGCACTAGGCAGGA	2186
rs143719502	snp	C/T	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67907763	AGTTCAATATGTATC[C/T]CTACGTAGACATTTT	2186
rs143731190	snp	A/T	4.94238e-05	0.00497086	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67894128	GTTAAACCAGTTGTG[A/T]TGCTACCAATATGGC	2186
rs143770213	snp	C/G	6.89406e-05	0.00587073	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67826179	AGGAGGACGGCGACG[C/G]CGAGGAGACCCAGGA	2186
rs143795367	snp	C/T	0.00398564	0.0444627	intron-variant	BPTF	GRCh38.p7	17:67893885	TGTACTTCTAACTTA[C/T]TGAACCGACACCACT	2186
rs143813665	snp	C/T	0.00557542	0.0525036	intron-variant	BPTF	GRCh38.p7	17:67964465	ATAATTTTGGAAGCA[C/T]TTCTAGGATTTCAAG	2186
rs143817835	snp	C/T	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67922719	ACAGCTGAGTAGCTG[C/T]AGCAGAGACCATCTG	2186
rs143837582	snp	C/T	0.0912534	0.193131	intron-variant	BPTF	GRCh38.p7	17:67978345	ACTCTGTTGCCCAGG[C/T]TGGAGTTCAGTGGCA	2186
rs143845836	snp	C/T	0.0345262	0.126772	intron-variant	BPTF	GRCh38.p7	17:67907443	TCACTGCAACCTCCA[C/T]CTCCCGGGTTCAATC	2186
rs143897895	snp	C/T	0.00597247	0.0543191	intron-variant	BPTF	GRCh38.p7	17:67925717	TAACTATTTAAAAAT[C/T]ATATATAAACCAAAT	2186
rs143911596	snp	C/T	1.66413e-05	0.0028845	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67911277	AAATGCAAATAATGA[C/T]CAACCTGAGGACTTG	2186
rs143922002	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67840259	TCAAGTGCGCACCTC[C/T]ACAGTTGGCTAATTT	2186
rs143937013	snp	C/G	0.000153988	0.00877327	missense	BPTF	GRCh38.p7	17:67944340	CCACCACAGCCAGCA[C/G]CACCACCACCACTGT	2186
rs143940568	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67933145	GTAATCCCAGCTACT[C/G]TACTCGGGAGGCTGA	2186
rs143960583	in-del	-/CT			intron-variant	BPTF	GRCh38.p7	17:67951193	AGCTTAACCTTCAGC[-/CT]CTCTCTCTCTCTCTT	2186
rs143972603	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67972944	TCTGTGTGTTTTCAC[A/G]GTTCTTCACATTTAC	2186
rs143981520	snp	A/G	9.04347e-05	0.00672378	missense	BPTF	GRCh38.p7	17:67945589	CTCAGCCTGAAGTTC[A/G]GACTCAGCCTGAAGT	2186
rs143983287	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	BPTF	GRCh38.p7	17:67823548	ACAGGCCTGAGCCAC[C/T]GTGCCTGACCACCCT	2186
rs143992255	snp	A/G	0.00636936	0.0560724	intron-variant	BPTF	GRCh38.p7	17:67894237	AGCCTATTAATAATG[A/G]AAGTTAATATATTTA	2186
rs143998649	snp	A/T	0.00517822	0.0506191	intron-variant	BPTF	GRCh38.p7	17:67890884	TGTCTTCATTTTTTT[A/T]AAGCTTTAAATTAAA	2186
rs144088804	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67895910	CAGGGTGTTCCTTAT[A/G]ATATTATTTCATAAT	2186
rs144089668	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67855833	TCAGAGCAGGGCATG[A/G]AAAGGAGAGTTGAAA	2186
rs144121706	snp	C/T	0.00636936	0.0560724	intron-variant	BPTF	GRCh38.p7	17:67893129	CAGTGAATAATAGTA[C/T]CTGACATGTAATAGG	2186
rs144142668	snp	C/T	0.0103295	0.0711199	intron-variant	BPTF	GRCh38.p7	17:67925762	TAGTTTTCCCTTTCA[C/T]TTTATAAAACATTTT	2186
rs144159017	snp	A/G	0.00716266	0.059414	intron-variant	BPTF	GRCh38.p7	17:67964816	CATCCTGGCTAACAC[A/G]GTGAAACCCCGTCTC	2186
rs144159292	snp	A/G			synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67911043	GACTAGTTACAAAAA[A/G]AAAACAAAATCATCC	2186
rs144178427	snp	A/G	0.00755907	0.0610114	intron-variant	BPTF	GRCh38.p7	17:67865198	CTTTTGGATCTTGGA[A/G]CATTTTGGATTTCAG	2186
rs144230611	snp	A/G	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67974338	CACGCTACGGTCAAC[A/G]TGGGAGAATTCTGTT	2186
rs144233864	snp	C/T	0.000153988	0.00877328	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67920071	AGGAGAGATGTTGGT[C/T]CTTATGGCATTCGAT	2186
rs144244744	snp	A/G	0.0023933	0.0345097	intron-variant	BPTF	GRCh38.p7	17:67903329	TTTAACAGTGACCTG[A/G]TTTAATAAATTATGG	2186
rs144332682	snp	A/G	0.000102957	0.0071741	synonymous-codon	BPTF	GRCh38.p7	17:67945413	CCTTTTTACAGGTAC[A/G]GGTGAACAAAGGCAG	2186
rs144356054	snp	A/G	0.00517822	0.0506191	intron-variant	BPTF	GRCh38.p7	17:67917836	TTTGTTTTTGAGACA[A/G]AGTCTCGCTCTGTCG	2186
rs144369168	in-del	-/GTGT	0.443548	0.158237	intron-variant	BPTF	GRCh38.p7	17:67878682	CGTCTTTATGTGTTC[-/GTGT]GTGTGTGTGTGTGTG	2186
rs144375265	snp	C/T	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67838289	ATTAGTCTGTGATTT[C/T]GATAATTCGTTTAGG	2186
rs144402529	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67882344	GTAGTGTTATGAAAG[A/G]CATATTTTTGAAAAG	2186
rs144424057	snp	A/G	0.0337553	0.125452	intron-variant	BPTF	GRCh38.p7	17:67954011	TTTTTTTGAGAAGCA[A/G]GGCCTTGTTCTGTTG	2186
rs144428920	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67946417	TGTTAGGTTTCCTAA[A/C]TGAGACAAAGTCATT	2186
rs144470906	snp	A/G	0.0670745	0.170406	intron-variant	BPTF	GRCh38.p7	17:67841366	GTGAGTCGAGATTGC[A/G]CCATTGCACTCCAGC	2186
rs144473392	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67915975	AAAGTCATTGTTTGA[C/T]CACAGAGAATGAGGA	2186
rs144485416	snp	A/G	0.00517822	0.0506191	intron-variant	BPTF	GRCh38.p7	17:67969189	CAGTGGCTCATGCCT[A/G]TAATCCCAGCACTTT	2186
rs144496749	snp	A/G	0.183886	0.241099	intron-variant	BPTF	GRCh38.p7	17:67908939	TCCTGGGTTCAAGCA[A/G]TTCTCCTGCCTCAGC	2186
rs144578624	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67868544	TGGTTGAATCCAAGG[A/G]TGCAGAACCTTTGGC	2186
rs144633999	snp	C/T	0.0337553	0.125452	intron-variant	BPTF	GRCh38.p7	17:67856179	TTTGTCTCTTTTTCT[C/T]TTTGGGGTATTTGTA	2186
rs144638228	snp	A/G	0.00557542	0.0525036	intron-variant	BPTF	GRCh38.p7	17:67920709	ATATCAGTGTTATAT[A/G]TGTTGCAGTAAGCTA	2186
rs144666885	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67960250	TGTTCAAAGCCCTGC[A/G]AATACATGAAATCCT	2186
rs144683858	snp	A/C	0.00478085	0.0486577	intron-variant	BPTF	GRCh38.p7	17:67853251	GAACAGGTATCTAAA[A/C]AGTTGTTTAACTGAC	2186
rs144690580	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67851219	GTCACAAGGGGCCTT[C/T]GTGACTGGGCTCAAG	2186
rs144698263	snp	A/C	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67892504	CATCCCAGCTCTGAT[A/C]ATGAACAATGGGATC	2186
rs144698927	snp	A/G	0.00636936	0.0560724	intron-variant	BPTF	GRCh38.p7	17:67916911	AAGTTCATTTAAGTA[A/G]AGTGAAAATGTCAAC	2186
rs144732548	in-del	-/ACTT	0.030665	0.119967	intron-variant	BPTF	GRCh38.p7	17:67922664	CAGCCACATTTACTC[-/ACTT]ACGTATTGTCTTTGG	2186
rs144769118	snp	A/G	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67959248	CCCAGATGGGACAGG[A/G]GCAAGCCAGGAGGGA	2186
rs144807262	snp	A/G	0.000329565	0.0128325	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911789	CTATTCAGGATAGCA[A/G]TGAAGAAGATATGAT	2186
rs144845654	snp	C/T	0.00517822	0.0506191	intron-variant	BPTF	GRCh38.p7	17:67945088	TCGCCCAGGCTGAAG[C/T]GAAGTAGCACCATTA	2186
rs144851860	snp	C/T	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67849611	TCTCAGAGTATGGTT[C/T]GCCAGAACAGCACAA	2186
rs144878560	snp	C/T	0.00478085	0.0486577	intron-variant	BPTF	GRCh38.p7	17:67924818	TCACCCAGGCTGGAG[C/T]AGATCACAGCTCACC	2186
rs144879949	snp	A/G	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67899103	GGCCAAACTTTTGTA[A/G]AATTACAGACCCACA	2186
rs144881136	in-del	-/GGG			intron-variant	BPTF	GRCh38.p7	17:67943185	GGTGACCACAGTGGC[-/GGG]GGTTTTATAGATGTT	2186
rs144882894	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67971805	TGCACTTCAGCCTGG[A/G]CAATAGAGTGAGACT	2186
rs144984934	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67919949	TTTTTGAAAGCACCA[C/G]ATGTACCTTTTTAGT	2186
rs145008089	snp	C/T	1.6473e-05	0.00286988	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67854500	ATACAGTATGATGAC[C/T]ATTGTAGGGTTTGTC	2186
rs145014617	snp	A/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67898205	TGAAACCCCATCTCT[A/G]CTAAAAATTAGCCAG	2186
rs145019699	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67940357	ATGGAAAAGAATACG[A/T]TCATGTGAGGTGTTG	2186
rs145024702	snp	A/G	0.000153988	0.00877328	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67854301	CATAGATGGGATGAC[A/G]TGGCCAGAGGTGCTG	2186
rs145032167	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67905982	TGCAGCACACCAACA[C/T]GGCACATGTATACAT	2186
rs145065851	snp	A/T	0.00914312	0.0669923	intron-variant	BPTF	GRCh38.p7	17:67899950	GCCAGGGAGTTGGAC[A/T]CACAAGCATCTGATG	2186
rs145078435	snp	A/G	0.00557542	0.0525036	intron-variant	BPTF	GRCh38.p7	17:67937178	TGAAAAGTACTGGCC[A/G]GGCGCGATAGCTCAC	2186
rs145098134	snp	A/C	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67884110	CAGCTTTTATTCAAC[A/C]AATGCCCTATTGATG	2186
rs145098863	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67836763	TAGACAGCAAAATTA[C/T]TTCACACACTTCTTA	2186
rs145113671	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67949658	ATATATATATACACA[C/G]AGACATATATATATA	2186
rs145159772	snp	A/T	0.00993419	0.0697739	intron-variant	BPTF	GRCh38.p7	17:67958581	AAAAATACAAAAAAT[A/T]AGCTGGGTATGGTGG	2186
rs145171467	snp	C/T	0.00636936	0.0560724	intron-variant	BPTF	GRCh38.p7	17:67955679	TAAAAATGCAAAAAT[C/T]AGCCAGACATGGTGG	2186
rs145233454	snp	A/T	0.000296623	0.0121747	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67911763	TTTGGAAAATAGTTC[A/T]GATACCGTGTCTATT	2186
rs145253980	snp	C/T	0.00716266	0.059414	intron-variant	BPTF	GRCh38.p7	17:67910764	GAGATCATGCCACTG[C/T]ACTCCAGCCTGGGCA	2186
rs145266502	snp	G/T	0.000444858	0.0149074	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67929413	CAAACCTTTACTTCA[G/T]TCCAGCCCAGGACAG	2186
rs145273025	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67883894	GTGAACCACCGCGCC[C/T]GGCTCGTTTTGTTTT	2186
rs145275678	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67956734	TTTGGGAGGCCGAGG[C/T]GGGCAGATCACGAGG	2186
rs145276365	snp	C/T	0.00953873	0.0683987	intron-variant	BPTF	GRCh38.p7	17:67921666	CTTGGGAGTTCTTCT[C/T]GGAGAATAACCTTTT	2186
rs145299599	snp	C/T	0.00517822	0.0506191	intron-variant, utr-variant-5-prime	BPTF	GRCh38.p7	17:67889339	AGGATTGACTCTGAG[C/T]AGTATTGGATTGTTG	2186
rs145360579	snp	A/C	0.0130921	0.0798413	intron-variant	BPTF	GRCh38.p7	17:67970845	TTTTTTATTGTGTGT[A/C]GTTTTTGCTAGTATA	2186
rs145394122	snp	G/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67880131	TTTATATATATAGGG[G/T]CTATACTCGCTCTAT	2186
rs145400357	snp	A/G	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67965753	GGATTATCAAGTGAT[A/G]CAGATGTACTGAAGA	2186
rs145406542	snp	C/T	0.00438332	0.0466095	intron-variant	BPTF	GRCh38.p7	17:67870485	AAATAGAAGAATTCC[C/T]GATTAAAACACCAGT	2186
rs145422614	snp	A/G	0.0023933	0.0345097	intron-variant	BPTF	GRCh38.p7	17:67886516	ACAGCACTTGCACTC[A/G]ATGTTTTTGTTTTCA	2186
rs145442631	in-del	-/A	0.0138799	0.0821421	intron-variant	BPTF	GRCh38.p7	17:67892623	GCAGGGTAGATATGC[-/A]AGAATAAAGGACATT	2186
rs145444712	snp	A/T	0.00358779	0.0422022	intron-variant	BPTF	GRCh38.p7	17:67893803	GTAGTTGTGCATTTG[A/T]AAACGTCATTACCAA	2186
rs145463211	snp	C/T			stop-gained, nc-transcript-variant	BPTF	GRCh38.p7	17:67911377	CTTTATCCAAAAGAT[C/T]GAGTGTTAGATGATG	2186
rs145519434	snp	C/T	1.64741e-05	0.00286998	missense	BPTF	GRCh38.p7	17:67945834	ACCTCACAACCGATT[C/T]CAATTCAACCACATA	2186
rs145536461	snp	C/T	0.000132007	0.00812317	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67928386	AGAAGCCGACAGTGA[C/T]TGCAACTTCCACTAC	2186
rs145540991	snp	C/T	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67960891	AAAACTCTTTGTTGG[C/T]AGATTGAGCTGTGTG	2186
rs145547051	snp	C/G	0.000798403	0.0199641	intron-variant, utr-variant-5-prime	BPTF	GRCh38.p7	17:67888737	TAATAAAACTGGATG[C/G]CATTGTTTTTCTGGG	2186
rs145555889	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67935611	AATAAAGTGAGCTTT[C/T]TTAACTCAAAAGGAA	2186
rs145584558	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67860992	CCCGTGCCTGAATTC[C/G]TTCTGTCCACGTTCA	2186
rs145604875	in-del	-/TATTGAG	0.0252325	0.109451	intron-variant	BPTF	GRCh38.p7	17:67881160	TCATGATACCCATTA[-/TATTGAG]TATTATCAGTGATCA	2186
rs145606454	in-del	-/C	0.440884	0.161442	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67897174	TCTACTTAAAAAAAA[-/C]AAAAACAAAAAACGA	2186
rs145616577	snp	C/G	0.0174175	0.0916809	intron-variant	BPTF	GRCh38.p7	17:67933554	AGCCTGGGAGACGGA[C/G]CACGACCTGTTTAAA	2186
rs145627837	snp	A/C/G	0.0138799	0.0821421	intron-variant	BPTF	GRCh38.p7	17:67850603	GGAACTCCTGACCTC[A/C/G]TGATCTGCCCACCTT	2186
rs145667824	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67830417	TGAACCATAGATTCA[A/C]ATTCAAGCAGAATTT	2186
rs145670702	snp	A/G	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67939084	CCTTTCAAAACTTCA[A/G]CTTAGTACTATATTC	2186
rs145711228	snp	A/G	0.00517822	0.0506191	intron-variant	BPTF	GRCh38.p7	17:67867618	TTCCTCTGGGTTGTC[A/G]GTTTCTCAGACTTTC	2186
rs145741599	snp	C/G			intron-variant, utr-variant-5-prime	BPTF	GRCh38.p7	17:67888977	AGTACTTAATGCCCA[C/G]TAACTTGCTTTAGGA	2186
rs145760651	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67842859	TTTCAGATGAAGAAA[A/C]TCTAAGAGAATGTGT	2186
rs145766181	snp	A/G	0.00597247	0.0543191	intron-variant	BPTF	GRCh38.p7	17:67879857	CCCAACACCCAACCC[A/G]AGAGCATTAATCTGC	2186
rs145781408	snp	A/T	0.00517822	0.0506191			GRCh38.p7	17:67951710	ATGTATGTATTCATA[A/T]ATAAACCTGTTTTAT	2186
rs145796024	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67953961	TTTTTCTTTTCTTTT[C/T]TTTTTTTTTTTTTTT	2186
rs145809187	snp	G/T	0.00279162	0.0372561	intron-variant	BPTF	GRCh38.p7	17:67862648	GTTTTATCAGTTTCC[G/T]GCAGCTGCTATAACA	2186
rs145859683	snp	A/G	0.00279162	0.0372561	intron-variant	BPTF	GRCh38.p7	17:67837711	CACCGTGCCCAGCCT[A/G]TGTGGTTTTAAATTA	2186
rs145864467	snp	A/G	0.00358779	0.0422022	intron-variant	BPTF	GRCh38.p7	17:67903581	TCTTATGGAAAGGAT[A/G]TAGTATTTCTTGTTT	2186
rs145870742	snp	A/G	0.000115328	0.0075928	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67928487	TCAGTTACAACTGGA[A/G]CCAAAATGGTACTAA	2186
rs145891866	snp	C/G	0.0429648	0.14013	intron-variant	BPTF	GRCh38.p7	17:67917300	ACCATACCCAGCTTA[C/G]TTTTAGTAGAGATGG	2186
rs145903888	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67958802	AAACCCCGTTTCTAC[C/T]AAAAATACAAAAAAA	2186
rs145915991	snp	A/G	0.00478085	0.0486577	intron-variant	BPTF	GRCh38.p7	17:67979230	GCTACAGAGAAAAAT[A/G]TTTACATTTTCGTAG	2186
rs145948575	snp	G/T	0.00478085	0.0486577	intron-variant	BPTF	GRCh38.p7	17:67849386	GGCTTGGGCCTGAGA[G/T]TCTGAATTTCTCTCA	2186
rs145949154	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67914175	TTTCCCCTTAGGCTT[C/T]GTTTTTGTGTGTCTT	2186
rs145987850	in-del	-/CT			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67887756	AAACTCTTTGTTTTC[-/CT]CTCTCTCTCACCTTT	2186
rs145989367	snp	A/C	0.00597247	0.0543191	intron-variant	BPTF	GRCh38.p7	17:67895943	TGAAATTTGGAAACA[A/C]TTCCTAAGTACTCAA	2186
rs146027079	snp	C/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67901244	AGGGAAAGCATGTTT[C/G]GGAAGATATCACTTA	2186
rs146028726	snp	C/T	0.0107246	0.0724382	intron-variant	BPTF	GRCh38.p7	17:67859660	ATCTGCAACTTGCAT[C/T]GTTTTAGCTGTTAAA	2186
rs146030885	snp	A/G	0.00676609	0.0577691	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67897588	AGAAAGGGACCCACC[A/G]AGCTCCTTTTGGGTG	2186
rs146071247	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67876732	GATCACTTGAACCCA[C/T]GAGGTAGAGGTTGCA	2186
rs146071651	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67896885	AGGGATACATCTCAA[A/G]GAACCAACCTAAAGA	2186
rs146075003	snp	A/G	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67831693	TAGTCATGGTGGGCA[A/G]GTAGTATTCTGGGTG	2186
rs146086030	snp	A/G	0.0352966	0.128072	downstream-variant-500B	BPTF	GRCh38.p7	17:67984685	CCAGTCTGGAGTGCA[A/G]TGATGCCATCTCGGC	2186
rs146113470	snp	A/G/T	0.0372196	0.131242	intron-variant	BPTF	GRCh38.p7	17:67949490	TGAGGCAGGATAATC[A/G/T]TTTGAACCTGGGAGG	2186
rs146140728	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67844616	ATGTTGCCCAGGCTG[A/G]GCTCAAACTCCTGAG	2186
rs146155430	snp	C/G	0.0111196	0.0737302	intron-variant	BPTF	GRCh38.p7	17:67954525	TAGTCTCCCTTACCC[C/G]CCAGAAACCCTAATG	2186
rs146190765	snp	A/G	0.00279162	0.0372561	intron-variant	BPTF	GRCh38.p7	17:67881953	CTCACTGCAACCTCC[A/G]CCTCCTGAGTAGCTG	2186
rs146194411	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67872395	TGTACAATGATTTGG[G/T]TAAGAAAAGCTATAG	2186
rs146204055	snp	C/G	0.0014653	0.0270278	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67912636	TAAAAGAAAAACCGT[C/G]ATCACAGAAGTCACC	2186
rs146232864	snp	A/G	0.0437281	0.141251	intron-variant	BPTF	GRCh38.p7	17:67926604	GCTGGGATTACAGGC[A/G]TGAGCCACCGCACCC	2186
rs146241932	snp	A/G	8.37093e-05	0.00646898	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912037	AAGCTAAAAAATACC[A/G]CTGACAAAAAGAATA	2186
rs146252302	snp	A/G	0.000153988	0.00877328	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911339	TTCTTAGAATGAGTG[A/G]TCCTAGTCATACCAC	2186
rs146259976	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	BPTF	GRCh38.p7	17:67824127	AGCCACCGCGCCCAG[C/T]ATCTTTTTTAAAAAA	2186
rs146274452	snp	A/G	0.00438332	0.0466095	intron-variant	BPTF	GRCh38.p7	17:67932751	TTTTTTAAACCCTAT[A/G]CATTTATGAGAAATT	2186
rs146298889	snp	A/G	4.97146e-05	0.00498546	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911452	ATTGAAAATGACATA[A/G]AAGAAAAAGTCTCTG	2186
rs146311755	snp	A/C	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67864248	AACAACTTTTCAGCC[A/C]GGTGCGGTGGCTCGT	2186
rs146353526	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67910526	TATTTTTGGCTGGGC[A/G]TGGTGGCTCATGCCT	2186
rs146356572	snp	A/G	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67980920	ACCAACACTTTGAGA[A/G]GCCAAAGCAGGCAGT	2186
rs146374860	snp	A/C	9.8837e-05	0.00702914	synonymous-codon	BPTF	GRCh38.p7	17:67964290	AAGTGAGGCAGAGCT[A/C]ATTGATGAGTATGTC	2186
rs146395314	snp	G/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67914269	CAGCTAGAAAAAAAA[G/T]TAAGTACTCTCTATA	2186
rs146431435	snp	C/T	3.55019e-05	0.00421304	missense	BPTF	GRCh38.p7	17:67945604	AGACTCAGCCTGAAG[C/T]TCAGACCCAAACAAC	2186
rs146444099	snp	A/G	1.64825e-05	0.00287071	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67929418	CTTTACTTCATTCCA[A/G]CCCAGGACAGCAACA	2186
rs146447453	snp	A/G	0.00478085	0.0486577	intron-variant	BPTF	GRCh38.p7	17:67893153	TAATAGGTACTTAAT[A/G]TGTGTTAGTTTTCTT	2186
rs146572674	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67946510	GTGGAACACTTCGTT[A/G]GATACATATAATATA	2186
rs146590452	snp	A/G	0.0115144	0.0749975	intron-variant	BPTF	GRCh38.p7	17:67981116	GTGAGCTGTGATTGC[A/G]CCACTGCACTCCAGA	2186
rs146590779	snp	A/C	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67939210	AGTTTAACAACAACA[A/C]CAAAAAGGTGTGGGG	2186
rs146615944	snp	C/G	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67838371	TTAAATTTTATTTTT[C/G]CTTCTTCTCTTTATC	2186
rs146616893	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67879501	GGAGTTTTCACTGTG[A/T]GAAGGTTATTATAGA	2186
rs146642163	snp	C/T	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67842231	TACATAGACATATAT[C/T]TACATACATTGACAG	2186
rs146651891	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67964431	CTGTGTGCAGCATTT[C/G]AAAATGAAATCAGCC	2186
rs146688656	snp	A/T	0.00478085	0.0486577	intron-variant	BPTF	GRCh38.p7	17:67924194	TCCTGATCTCAAGCA[A/T]TCCACCTGCCTCGGC	2186
rs146708019	snp	A/C	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67920904	ATATTTAGGAAAAAA[A/C]CTAGTAAGAAATATA	2186
rs146746807	snp	A/G	1.65386e-05	0.00287559	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	BPTF	GRCh38.p7	17:67893426	CACCAAAAAGGAAGT[A/G]ATCATGAAAGGAAAT	2186
rs146757298	snp	A/G	0.0111196	0.0737302	intron-variant	BPTF	GRCh38.p7	17:67892979	GATGTTTTTAGGAAT[A/G]TATTTTTTGGGGGAT	2186
rs146758771	snp	C/T	3.29457e-05	0.00405854	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67854430	TCTACAGTTTCTAGT[C/T]GATCAGTTTCTTACA	2186
rs146795207	snp	C/T	4.98451e-05	0.004992	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67893612	AGAGTTCAAATGGAA[C/T]GGTTCTGTCCATGGG	2186
rs146805567	snp	A/C/T	3.32023e-05	0.00407434	synonymous-codon, missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67854725	GGATATGATAGAAGT[A/C/T]GGAGGAAATACTGGT	2186
rs146828725	snp	C/T	0.0372196	0.131242	intron-variant	BPTF	GRCh38.p7	17:67906021	AACCTGCACGTTGTG[C/T]GCACGTACCCTAGAA	2186
rs146831078	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67975173	ATCTATCACCATAAT[G/T]ATTTTCTCCTTTCTG	2186
rs146831818	snp	A/G	0.0023933	0.0345097	intron-variant	BPTF	GRCh38.p7	17:67894322	TAAACATGAATGAAT[A/G]TTATTAGTTCTTTCT	2186
rs146837881	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67870691	AATAATTTACAGCAT[A/G]ACAGGAATTTCAGAA	2186
rs146846591	snp	C/G	0.0111196	0.0737302	intron-variant	BPTF	GRCh38.p7	17:67964549	CTAACAAACTGCAGT[C/G]CTTCACGTACCAGTG	2186
rs146875632	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67858587	AAAAAAAGTTTACTG[C/T]TGTGTTGTCATTGTA	2186
rs146878308	snp	A/G	0.0103009	0.0710235	intron-variant	BPTF	GRCh38.p7	17:67874784	TTTGGTTATATATAG[A/G]AATAATTTTTTTGTT	2186
rs146879804	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67961471	TCCAGAACACAGCCT[-/T]ATCACCCTGTGGAGA	2186
rs146904660	snp	C/G	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67966253	TTTGAACCCATCCCA[C/G]CTGTTGACAGAAGCG	2186
rs146941919	snp	A/G	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67827339	GTAATGAATTTCTCC[A/G]TGGTAACCCCTCTTC	2186
rs146953123	in-del	-/CCT			intron-variant	BPTF	GRCh38.p7	17:67840493	GCTGCTGCTCCTCCG[-/CCT]CCTCCTCCTTCCCCT	2186
rs146991470	snp	A/G	0.00438332	0.0466095	intron-variant	BPTF	GRCh38.p7	17:67876976	GAAGATGCTGTACCT[A/G]CAAATTCAAAACCTT	2186
rs146993504	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67947943	CACTAATAGTTACTC[A/G]TAACTGGTTTGAACC	2186
rs147014694	snp	C/G	0.00517822	0.0506191	intron-variant	BPTF	GRCh38.p7	17:67881458	AGATTCTCTGTTAAC[C/G]TCTCACTCATTAATA	2186
rs147034943	snp	C/T	0.000447046	0.014944	missense	BPTF	GRCh38.p7	17:67959716	CAGGCCTTCTGTCCA[C/T]GCCCACCTTACCTGC	2186
rs147061402	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67967251	GGTTCAAGCAATTCT[C/T]CTGCCTCAGCCTCCC	2186
rs147096467	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67925458	CCCTTGAGTCCAGGG[A/G]TTTGAGACCAGCCTG	2186
rs147096891	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67970838	AATAGATTTTTTTAT[C/T]GTGTGTAGTTTTTGC	2186
rs147119383	snp	A/G	0.00993419	0.0697739	intron-variant	BPTF	GRCh38.p7	17:67929223	CGGATCTCACATTCT[A/G]TGTAGCCCACTATAA	2186
rs147125121	snp	C/T	0.00184502	0.0303167	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67911820	TGTTCAGAATAGCAA[C/T]GAAAGCATTTCTGAA	2186
rs147131865	snp	A/G/T	0.0123036	0.0774623	intron-variant	BPTF	GRCh38.p7	17:67943348	GCGCCATCAGTTTTG[A/G/T]TCATTGGGAGTTTAG	2186
rs147167486	snp	A/G	0.00517822	0.0506191	intron-variant	BPTF	GRCh38.p7	17:67949273	GGGAGGCTAAGGCAG[A/G]ATGATCACTTGAACC	2186
rs147167652	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67902816	TAACAAAAGGTCTCT[A/G]TTCTTTCTGCAGAGC	2186
rs147173000	snp	C/T	0.00279162	0.0372561	intron-variant	BPTF	GRCh38.p7	17:67837024	CATGAGTTGTGAATC[C/T]TCTCTGTGTCTCAGA	2186
rs147269227	snp	C/T	0.00438332	0.0466095	intron-variant	BPTF	GRCh38.p7	17:67891598	AGATGAGTTTTTAAA[C/T]AGATAACCCAGCATG	2186
rs147270520	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67849797	ACAAAAAAAATTAGC[C/T]GGGCATGGTGGTGGG	2186
rs147271932	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67962188	ACTACATAACCATAT[A/G]TTATTCCTTCACATT	2186
rs147274081	snp	A/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67888084	CAAATATTATAGCAT[A/G]GTAAATATCTACACT	2186
rs147356560	snp	A/G	8.27246e-05	0.00643082	synonymous-codon, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67875629	AACAAATGCAACTTC[A/G]GAAGAGACTAGTCCC	2186
rs147366402	snp	C/T	1.6473e-05	0.00286988	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67854094	GGTACTGCGGAACTT[C/T]GGCACTGTTTTGAGA	2186
rs147376430	snp	A/G	0.0111196	0.0737302	intron-variant	BPTF	GRCh38.p7	17:67872829	TAAGGGCTGGGCACT[A/G]CTAACGCCTGTAACC	2186
rs147378367	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67942304	TAGGCAACAGACTCC[A/G]TCTCAAAAAAAAGAA	2186
rs147380480	snp	G/T	0.0111196	0.0737302	intron-variant	BPTF	GRCh38.p7	17:67936892	TGAGTAATTTCCCAA[G/T]CTATTAATCTGGGAT	2186
rs147412359	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67836630	CAAAATACATGAGGA[A/C]TGATAAAACTCCAAG	2186
rs147436037	snp	C/T	0.00358779	0.0422022	intron-variant	BPTF	GRCh38.p7	17:67839203	AAATGTTAGTTATAA[C/T]GATAGGCATCTTAGT	2186
rs147446457	in-del	-/A			intron-variant	BPTF	GRCh38.p7	17:67978304	AATATATATATATAT[-/A]TATATTTTTTTTGAG	2186
rs147449680	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67962318	GCAAGGCCAGTCTGG[C/T]TCCCTGTGATTCATG	2186
rs147465771	snp	A/G	1.64732e-05	0.0028699	synonymous-codon	BPTF	GRCh38.p7	17:67944254	CCCAGGCCCAGGCCA[A/G]CAGCTAATGCAAGCT	2186
rs147471740	snp	A/G	6.59196e-05	0.00574068	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67922910	ACCAGAAACGCCCAA[A/G]CAAACTGGCCCTGTT	2186
rs147472503	snp	A/G	0.0103295	0.0711199	intron-variant	BPTF	GRCh38.p7	17:67857280	CATTCTCCTGCCTCA[A/G]CCTCCGAGTAGCTGG	2186
rs147482332	snp	A/G	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67922535	GGAATAGTGCTCCAG[A/G]TGGAAGAAACAGGTT	2186
rs147485857	snp	A/C	0.00517822	0.0506191	intron-variant	BPTF	GRCh38.p7	17:67918223	TTACAGGCGTGAGCC[A/C]CCGCATCTGACCTCA	2186
rs147488645	snp	C/T	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67853521	ATCTATTGCCCCTAC[C/T]TTGTGCTGTGTATCT	2186
rs147548086	in-del	-/C			intron-variant, frameshift-variant	BPTF	GRCh38.p7	17:67929062	AAAGTAATTACCAAA[-/C]CTGCCACTTCCTGCA	2186
rs147553910	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67898250	GCCTTTAGTCCCAGC[C/T]ACTAGGAGGCTGAGG	2186
rs147563155	snp	A/G	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67975106	CGTGTTAGGAGCTAA[A/G]TGTCAGGAAATGGGG	2186
rs147572193	snp	A/T	0.0107246	0.0724382	intron-variant	BPTF	GRCh38.p7	17:67835830	GCCACCATGCCCGGC[A/T]AATTTTTTGTAATTT	2186
rs147586034	in-del	-/AAT			intron-variant	BPTF	GRCh38.p7	17:67883317	CGAGACTCCATCTAA[-/AAT]AATAATAATAATAAT	2186
rs147595686	in-del	-/TTA			intron-variant	BPTF	GRCh38.p7	17:67841835	TTTAGGTTTCCTATT[-/TTA]TTATTTGTTTTCTGA	2186
rs147635939	snp	A/T	0.00517822	0.0506191	intron-variant	BPTF	GRCh38.p7	17:67960561	AAACCGTAAATGTAG[A/T]TTCATTTTTTTGGTC	2186
rs147639955	snp	C/T	0.00557542	0.0525036	intron-variant	BPTF	GRCh38.p7	17:67847140	AGTAATAATGGTATC[C/T]ATTTTATGGAGTTGA	2186
rs147659005	snp	A/G	0.0115144	0.0749975	intron-variant	BPTF	GRCh38.p7	17:67883449	ATGTAGAGCATTTAC[A/G]TTATTATAAATTGAA	2186
rs147740443	snp	C/T	0.0399052	0.1355	intron-variant	BPTF	GRCh38.p7	17:67896197	TCCATCTCCTGACCT[C/T]GTGATCCGCCCGCCT	2186
rs147756467	snp	A/G	0.0372196	0.131242	intron-variant	BPTF	GRCh38.p7	17:67933576	CTGTTTAAAAAAAAA[A/G]AAAAAAAGAAAAAAA	2186
rs147763269	snp	A/G	0.0341408	0.126114	intron-variant	BPTF	GRCh38.p7	17:67933465	TCCCAGCTACTTGGT[A/G]GGCTGAGATGGGAGG	2186
rs147780387	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67865452	AGGCAGGTTTTATTA[C/T]ATCTTCATTTTACAA	2186
rs147803346	snp	C/G	0.00279162	0.0372561	intron-variant	BPTF	GRCh38.p7	17:67826484	GCGACGGCACATCAA[C/G]TGGCAAAAAACTAGA	2186
rs147843964	snp	C/G	0.0111196	0.0737302	intron-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67919287	TCACCTGTAATCCTA[C/G]CACTTTGGGAGGCCA	2186
rs147844799	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67880834	ACCCTCTATCAGAGA[A/G]CATTCTATGCATGAT	2186
rs147860792	snp	A/G	0.00636936	0.0560724	intron-variant	BPTF	GRCh38.p7	17:67916060	TCTCTAGGAATTACT[A/G]TGGGGTATGGTCTGA	2186
rs147869065	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67915495	TAATGCTCTTCTTTA[A/T]TCTTTTATTTTGGTA	2186
rs147885480	snp	A/G	0.0337553	0.125452	intron-variant	BPTF	GRCh38.p7	17:67850472	CTCCTGGGTTCAAGC[A/G]GTTCTTCTGCCTCAG	2186
rs147928104	snp	G/T	8.32258e-05	0.00645027	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912751	GAAAATTGTGCAAAA[G/T]CCACTGTCACAACCA	2186
rs147952007	snp	A/G	0.000305412	0.0123537	intron-variant	BPTF	GRCh38.p7	17:67928319	TTTTTATTTAGAACT[A/G]TTTTGATTCATGTTT	2186
rs147952489	snp	A/C	0.00478085	0.0486577	intron-variant	BPTF	GRCh38.p7	17:67974372	CGGCCTCTGGTCAGC[A/C]AGAAGTGGGTGGGGA	2186
rs147965972	in-del	-/GTTTTTG	0.024059	0.107008	intron-variant	BPTF	GRCh38.p7	17:67880617	CATTTGTAGGTTTTT[-/GTTTTTG]GTTTTTGGTTTTTGG	2186
rs148000856	snp	A/G	0.095934	0.196885	intron-variant	BPTF	GRCh38.p7	17:67956515	TAGAGATGGTGTTTC[A/G]CCACGTTGGCCAGGC	2186
rs148022265	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67906369	CAGGTGTGACCACTG[C/T]GCCTGGCCTATAAAT	2186
rs148027363	snp	C/G	0.0322114	0.122752	intron-variant	BPTF	GRCh38.p7	17:67881528	TTTTTGAGAGACAGA[C/G]TCTCGCTCTGTCACC	2186
rs148031124	snp	C/T	0.00597247	0.0543191	intron-variant	BPTF	GRCh38.p7	17:67977387	AGGCATAATGGTGCA[C/T]GCCTGTAGTCTCAGC	2186
rs148040962	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67898711	AATTATTATGCCTTT[-/T]GGTGAAACCCTTGAA	2186
rs148120916	snp	C/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67967477	CCAGCAGTTTCATTT[C/G]TTAGGATTTACATGT	2186
rs148161698	snp	A/G	0.0189856	0.0955633	intron-variant	BPTF	GRCh38.p7	17:67857138	TATCCTTATGAGTTC[A/G]TCTTTAACAATTTTT	2186
rs148162720	snp	C/T	6.86683e-05	0.00585913	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67826180	GGAGGACGGCGACGC[C/T]GAGGAGACCCAGGAT	2186
rs148162772	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67921753	ACTTAAAACAGCGGC[C/T]AGGTGCGGTGGCTTC	2186
rs148169980	snp	A/G	3.29875e-05	0.00406112	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911849	AACAGTTCAGAACTC[A/G]AGAACAAGATGTTGA	2186
rs148179750	snp	G/T	0.00557542	0.0525036	intron-variant	BPTF	GRCh38.p7	17:67964467	AATTTTGGAAGCATT[G/T]CTAGGATTTCAAGTT	2186
rs148194795	in-del	-/CTTAAA	0.040671	0.13668	intron-variant	BPTF	GRCh38.p7	17:67851709	AGTTATAAGCAGAAC[-/CTTAAA]CTTGACAATCCTGAA	2186
rs148199966	snp	C/T	0.00755907	0.0610114	utr-variant-3-prime, downstream-variant-500B	BPTF	GRCh38.p7	17:67983501	TCATCCTCTGTGTTA[C/T]TTGTTGATTGGGTTT	2186
rs148235412	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67941650	GTAAATGGTGCCAGG[A/G]CAATTGAATATACAT	2186
rs148236815	snp	A/G	0.0107246	0.0724382	intron-variant	BPTF	GRCh38.p7	17:67848387	TCAACAAATGAGCCA[A/G]GGGGCATGAGTAATT	2186
rs148259687	snp	A/G	3.49296e-05	0.00417895	missense	BPTF	GRCh38.p7	17:67940439	TTGCTGTTTGGGTAG[A/G]TGCTCCTCAGCAAGT	2186
rs148284560	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67901809	ACTGTTCTGAAGAGT[A/C]GTTTGACCCTATATC	2186
rs148288638	snp	A/G	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67971534	TTTAGGGCCGGGCAC[A/G]GTGGCTCATGCCTGT	2186
rs148325405	snp	A/G/T	0.00716625	0.0594738	intron-variant	BPTF	GRCh38.p7	17:67838581	TCTTAGGTTCAGGTG[A/G/T]TTCTCTTGCCTCAGC	2186
rs148335836	snp	C/T	0.00755907	0.0610114	intron-variant	BPTF	GRCh38.p7	17:67863575	AGGCGTGAGCCACCA[C/T]GCCCGGCCCATTACC	2186
rs148337978	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67931304	TCTCTAAATAAGTAA[A/G]TGAATGAATGAATGA	2186
rs148388833	snp	C/G	0.00993419	0.0697739	intron-variant	BPTF	GRCh38.p7	17:67924899	GACTACAGGCACACA[C/G]CACCATGCCCAGCTA	2186
rs148437340	snp	C/G	0.095934	0.196885	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67897960	AAATCTGAAAATATT[C/G]GTATGCAGATATATT	2186
rs148438779	snp	G/T	0.00835141	0.0640778	intron-variant	BPTF	GRCh38.p7	17:67969830	GCTCAGGAGGCTGAG[G/T]CAGGAGAATCGCTTG	2186
rs148458894	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67861615	GCCACCATGCCCAGC[C/T]ATAGCTGGATGATTT	2186
rs148490525	snp	C/G/T	0.00874735	0.0655527	intron-variant	BPTF	GRCh38.p7	17:67964815	CCATCCTGGCTAACA[C/G/T]GGTGAAACCCCGTCT	2186
rs148495574	snp	A/C/G	3.29458e-05	0.00405857	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67854319	GCCAGAGGTGCTGCG[A/C/G]GTGTACTGTGAGAGT	2186
rs148511710	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67949660	ATATATATACACACA[C/G]ACATATATATATATA	2186
rs148512501	snp	C/T	0.00438332	0.0466095	intron-variant	BPTF	GRCh38.p7	17:67892513	TCTGATCATGAACAA[C/T]GGGATCAGAGCTAGG	2186
rs148515277	in-del	-/CC			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67896466	ATGAGTAACTAGAAA[-/CC]CTGTCCCCCCAGTGC	2186
rs148548520	snp	A/G	0.00636936	0.0560724	intron-variant	BPTF	GRCh38.p7	17:67849697	AATCCCATAACTTTG[A/G]GAGGCTAAGGCGGGT	2186
rs148549917	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67914581	GTAACTTCTTTCCCA[C/T]TGGAAAAGTTACTAT	2186
rs148557840	snp	C/T	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67945162	CACCTCAGCCTCCCA[C/T]GTAGCTTGGACCATA	2186
rs148566338	snp	A/G	0.00559967	0.0526163	intron-variant	BPTF	GRCh38.p7	17:67959498	AGATCACACATTTAC[A/G]TGACTCTAATGATAG	2186
rs148646895	snp	C/T	0.0236746	0.106192	intron-variant	BPTF	GRCh38.p7	17:67933172	CTGAGGCAGGAGAGT[C/T]GCTTGAACCCAGGAG	2186
rs148648209	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67840383	AGGTGCTGAGATTAC[A/G]GGCATGAGCTGCCAT	2186
rs148669778	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67896002	GGAGTCTCGCTCTGT[C/T]ACCCAGGCTGGAGTG	2186
rs148685414	snp	C/T	3.29484e-05	0.00405871	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67854328	GCTGCGGGTGTACTG[C/T]GAGAGTGATAAGGAG	2186
rs148696633	snp	C/T	8.28013e-05	0.0064338	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67912372	AGATGCTGAAGGTAA[C/T]TACCGAGATAGCCTT	2186
rs148721507	snp	C/T	0.0126979	0.078662	intron-variant	BPTF	GRCh38.p7	17:67857408	CTTGTGATCTGTCTG[C/T]CTCGGCCTCCCAAAG	2186
rs148722280	in-del	-/TA	0.00795532	0.062565	intron-variant	BPTF	GRCh38.p7	17:67878145	ACTGGAACCATACAG[-/TA]TATATACTCTTTGAT	2186
rs148728817	snp	C/T	0.000494307	0.0157133	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67922903	CAAAGAGACCAGAAA[C/T]GCCCAAGCAAACTGG	2186
rs148757875	snp	C/G	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67882452	ATATCTGTTCCCTTA[C/G]ACTGAAAGCCTCAGT	2186
rs148759485	snp	A/C/G	8.50102e-05	0.00651904	missense	BPTF	GRCh38.p7	17:67945420	ACAGGTACAGGTGAA[A/C/G]AAAGGCAGAGTAAAC	2186
rs148769680	snp	G/T	0.00636936	0.0560724	intron-variant	BPTF	GRCh38.p7	17:67978434	CTCCCAAGTAGCTGG[G/T]ATTACAGGCAGCCAC	2186
rs148774857	snp	C/G	0.0142736	0.0832652	intron-variant	BPTF	GRCh38.p7	17:67917842	TTTGAGACAGAGTCT[C/G]GCTCTGTCGCCTAGG	2186
rs148821862	snp	A/G	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67856383	TTTCTGAGGCTATTA[A/G]TGACAGGTTTTTTTC	2186
rs148824178	snp	G/T	0.00557542	0.0525036	intron-variant	BPTF	GRCh38.p7	17:67893848	TCAATGTGGTCAGCA[G/T]ACAGGACATTAGAGG	2186
rs148833853	in-del	-/A	0.0111196	0.0737302	intron-variant	BPTF	GRCh38.p7	17:67898465	GGTTTTTTTATTTTT[-/A]ATTTTTTTACATTTT	2186
rs148864739	snp	C/G	1.64746e-05	0.00287002	intron-variant, missense	BPTF	GRCh38.p7	17:67946059	TCTCAGATCCAGTCA[C/G]AGGTTGTGGCTCAGA	2186
rs148885231	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67973897	ATACAGTTAAATCTG[-/T]TCCTGTTTTGAACTT	2186
rs148914370	in-del	-/G/T	0.00558989	0.0525709	intron-variant	BPTF	GRCh38.p7	17:67886375	TTTTTTTCTTTTTTT[-/G/T]TGTGTGTGTGTGTGT	2186
rs148926675	snp	A/G	0.0107246	0.0724382	intron-variant	BPTF	GRCh38.p7	17:67879965	GAGATTTTTGGCAGG[A/G]CAAACATCTAAACTA	2186
rs148927762	snp	A/G	0.00597247	0.0543191	intron-variant	BPTF	GRCh38.p7	17:67951924	GCTGGGCATGGTGGC[A/G]CACAACTGTAGTTCC	2186
rs148954198	snp	C/T	0.000533734	0.0163273	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67893696	CAACATCCCTTCATC[C/T]TTTCTTCATCCCAAC	2186
rs148962814	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67843106	CATATATCTATATAT[A/G]TGTAGATGTATGTAG	2186
rs149018701	snp	C/T	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67837838	AAATACACTCACTTG[C/T]GATGTGATATGAGAC	2186
rs149035359	snp	C/T	0.0111196	0.0737302	intron-variant	BPTF	GRCh38.p7	17:67924825	GGCTGGAGTAGATCA[C/T]AGCTCACCGAGCCTC	2186
rs149081556	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67979134	ATCTTCATGCCACTG[C/T]ACTCCAGCCTGGAAG	2186
rs149082560	snp	C/T	0.00993419	0.0697739	intron-variant	BPTF	GRCh38.p7	17:67884216	AATCTCAGCTCACTG[C/T]AACCTCAGCCTCCCA	2186
rs149087269	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67920613	GAGCACCAGTACAAT[A/G]GGCACTGGGTGGCAA	2186
rs149131927	snp	C/T	0.0379877	0.132479	intron-variant, utr-variant-3-prime	BPTF	GRCh38.p7	17:67981699	GTCCTTTGACTTAGT[C/T]CTGGTAACTGTACAG	2186
rs149169035	snp	C/T	4.94434e-05	0.00497184	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67911769	AAATAGTTCTGATAC[C/T]GTGTCTATTCAGGAT	2186
rs149172007	snp	C/T	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67876158	TATAGCATTTCAAAC[C/T]GTAGTATTATGGTAG	2186
rs149192516	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67863297	TTTCTTTTTCTTTTC[A/G]TTTTTTTGAGACACG	2186
rs149210375	snp	A/C/G	0.00438332	0.0466095	intron-variant	BPTF	GRCh38.p7	17:67966019	ATGATCACGCCACTC[A/C/G]ACACCAGCCTGAATG	2186
rs149226396	snp	A/G	0.00438332	0.0466095	intron-variant	BPTF	GRCh38.p7	17:67870486	AATAGAAGAATTCCC[A/G]ATTAAAACACCAGTT	2186
rs149258479	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67936504	GTTGCATAATGCCCT[A/G]TGTAGCTGTAAGTAT	2186
rs149278101	snp	A/C	0.000418652	0.014462	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912035	TAAAGCTAAAAAATA[A/C]CACTGACAAAAAGAA	2186
rs149315626	snp	A/G	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67906143	CTGGAGTGCAGTGGC[A/G]TATCTGGCCTCACTG	2186
rs149331683	snp	C/T	0.000153988	0.00877328	missense, nc-transcript-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67918830	CAGGAGGAGGGACTA[C/T]ACGGACAGGTAAGGG	2186
rs149394508	snp	A/G	3.29478e-05	0.00405867	synonymous-codon	BPTF	GRCh38.p7	17:67964275	CGTTGGCATCTTGCA[A/G]AGTGAGGCAGAGCTC	2186
rs149398277	snp	G/T	0.0023933	0.0345097	intron-variant	BPTF	GRCh38.p7	17:67885745	TAAGCTTCAGATTTT[G/T]AATACTATCTCAGCA	2186
rs149400195	snp	A/G	0.0111196	0.0737302	intron-variant	BPTF	GRCh38.p7	17:67959174	GCAAGAGCAACTAGA[A/G]GAAAGCAGCCAGTGA	2186
rs149421686	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67849605	GGTGTTTCTCAGAGT[A/G]TGGTTCGCCAGAACA	2186
rs149451348	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67913718	CTCTAAGATTCCTTA[C/G]AAATTTTTTTAAACC	2186
rs149472838	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67972840	TAATATAAGTATGAA[C/T]CAAGAATGTCCTAGT	2186
rs149475528	snp	G/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67878113	ACCACTGATTGGTTT[G/T]CCTTTTTTAAAAAAA	2186
rs149482106	snp	A/G	0.00101805	0.0225386	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911182	TCTACAAATTCTTCA[A/G]AAAATCTCTCTGAAT	2186
rs149528471	snp	A/T	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67941138	GATTATTTGCCCTAT[A/T]TATGATAACTTGATA	2186
rs149545379	snp	C/T	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67871693	AATGTTCATGCAAAG[C/T]ATAGAATATACTTGT	2186
rs149561756	snp	A/G	0.0142736	0.0832652	intron-variant	BPTF	GRCh38.p7	17:67857399	TCTCCTGACCTTGTG[A/G]TCTGTCTGCCTCGGC	2186
rs149562714	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67868407	AGAGCCCTCTGCAGA[C/T]AGCAAAATCCATGGA	2186
rs149565165	snp	A/G/T	0.0103295	0.0711199	intron-variant	BPTF	GRCh38.p7	17:67895589	CACCTCAGCCTCCTG[A/G/T]GTAGTTGGGACTACA	2186
rs149574058	snp	C/T	0.0498117	0.149749	intron-variant	BPTF	GRCh38.p7	17:67964771	TTTGGGAGGCCAAGG[C/T]GGGCGGATCACAAGG	2186
rs149598175	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67846719	GGTTTGTTTGTTTGT[-/T]TTGGAGACAGGGTCC	2186
rs149625281	snp	A/G	0.00517822	0.0506191	intron-variant	BPTF	GRCh38.p7	17:67962092	AGGCTGCAGGGGGCC[A/G]TGATCCTGCCCCTGC	2186
rs149637646	snp	A/G	0.000280581	0.0118411	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67866684	TTTCTGGCGGCAGCT[A/G]ATGGTGAGAGGGGCA	2186
rs149669594	snp	C/T	0.0107246	0.0724382	intron-variant	BPTF	GRCh38.p7	17:67837699	ACAGGCGTGAGCCAC[C/T]GTGCCCAGCCTATGT	2186
rs149704276	snp	A/G	0.000312966	0.0125054	missense	BPTF	GRCh38.p7	17:67945819	CAGGTTCAGACTACA[A/G]CCTCACAACCGATTC	2186
rs149719620	snp	A/G	1.67097e-05	0.00289043	missense, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67891993	CAGCAGGTGGCAGCC[A/G]CTGCACATGAAGCAA	2186
rs149722054	snp	A/G	0.0193772	0.0965046	intron-variant	BPTF	GRCh38.p7	17:67832849	CTGGAGTGGAGTGGC[A/G]GGATCTCAGCTCACT	2186
rs149737375	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67850602	CGGAACTCCTGACCT[C/T]GTGATCTGCCCACCT	2186
rs149767924	snp	C/G	0.00597247	0.0543191	intron-variant	BPTF	GRCh38.p7	17:67915391	GGGGAAAGCATTTGT[C/G]ACCTGTAGATCACAT	2186
rs149790901	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67879854	ACCCCCAACACCCAA[A/C]CCGAGAGCATTAATC	2186
rs149839335	snp	C/T	8.2464e-05	0.00642069	intron-variant	BPTF	GRCh38.p7	17:67944143	ACATGTTGTGTTTTT[C/T]CCACAGGGTGGCAAT	2186
rs149844960	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67874158	AATATCCATGAGTGC[A/G]TACTGATATACCGTG	2186
rs149851810	in-del	-/ATT	0.0551013	0.156571	intron-variant	BPTF	GRCh38.p7	17:67832642	CAGAGTTGTGCAACC[-/ATT]ATTAACACTACCTAA	2186
rs149856658	snp	G/T	0.00517822	0.0506191	intron-variant	BPTF	GRCh38.p7	17:67980884	CAAATTAGGCTGTGT[G/T]CAATGGTGCATGCCT	2186
rs149859677	snp	A/G	0.118933	0.212888	intron-variant	BPTF	GRCh38.p7	17:67843214	TACATGTAGATGTAT[A/G]TAGATATATACCTAT	2186
rs149862460	snp	C/T	1.64768e-05	0.00287021	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67928432	TACAACCAGCACCAT[C/T]TCTCCAGCACAGAAG	2186
rs149889378	snp	G/T	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67870407	GCTCAACTAGGTGTT[G/T]TACAATTCTTTAATC	2186
rs149922760	snp	C/T	0.000307953	0.0124049	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67854265	TGATCTGAAAGATAG[C/T]GTTAATTCCACACTG	2186
rs149929461	snp	C/G	0.0126979	0.078662	upstream-variant-2KB	BPTF	GRCh38.p7	17:67824931	CATTGGAGTCATTTT[C/G]TGGACTCCAGCTCCA	2186
rs149932892	snp	C/G	0.00676609	0.0577691	intron-variant	BPTF	GRCh38.p7	17:67864854	CTGTCACCCAGGCTA[C/G]AGTGAACTGGCGCGA	2186
rs149943074	snp	A/G	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67932978	AAAGATCAGCCAGGC[A/G]CAGTTGCTCATGCCT	2186
rs149960768	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67919945	TCTCTTTTTGAAAGC[A/T]CCAGATGTACCTTTT	2186
rs150002941	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67845346	TCAGTTACACCTCTG[A/G]TTGCAAATGGTGACT	2186
rs150014444	snp	G/T	0.0154538	0.0865337	intron-variant	BPTF	GRCh38.p7	17:67955632	AGGAGTTCGAGACCA[G/T]CCTGGCTAACAGGGC	2186
rs150051409	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67978149	GTGAGCCACCGCACC[C/T]GGCCATGATGTATCT	2186
rs150091415	snp	A/G	0.000153988	0.00877328	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67911922	CACTGGAAACTGTGA[A/G]GACAGGCTGCCGGTC	2186
rs150102906	snp	C/T	0.0111196	0.0737302	intron-variant	BPTF	GRCh38.p7	17:67881711	GTTTCACATGTTGGC[C/T]AGGCTGGTCTTGAAC	2186
rs150144995	snp	C/T	1.64762e-05	0.00287016	missense, nc-transcript-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67918812	TGGCGGCCAAGGCTC[C/T]TCCAGGAGGAGGGAC	2186
rs150152421	snp	A/G	0.00953873	0.0683987	intron-variant	BPTF	GRCh38.p7	17:67844274	TTTTTTTGAGACGGA[A/G]TCTAGCTCTGTTGCC	2186
rs150163906	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67947307	CGCTAATCTTTGTAT[A/G]GGGGAGACGAGGGAC	2186
rs150183831	snp	A/G	0.00279162	0.0372561	intron-variant	BPTF	GRCh38.p7	17:67967798	CATTCCAGCCTGGAC[A/G]ACAGAGCGAGACTCT	2186
rs150205013	snp	A/T	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67871522	TATATTTGTAACTAA[A/T]TATACAGCTTACTAT	2186
rs150241986	snp	A/G	0.00517822	0.0506191	intron-variant	BPTF	GRCh38.p7	17:67829019	AACTTGTAATAGATG[A/G]AGTTTTGATAACTCT	2186
rs150251003	snp	A/G	1.66527e-05	0.00288549	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67909736	TGAAATGGATATCTC[A/G]AAGATTACTGAGAAG	2186
rs150253288	snp	C/T	0.00993419	0.0697739	intron-variant	BPTF	GRCh38.p7	17:67934283	AGCACTTTGGGAGGC[C/T]AAGATGGGCAGATCA	2186
rs150257868	snp	C/G	0.00636936	0.0560724	intron-variant	BPTF	GRCh38.p7	17:67866191	TGTTACATTGATGAT[C/G]TTAAAGTTGGTTGAG	2186
rs150259187	in-del	-/AAGAC			intron-variant	BPTF	GRCh38.p7	17:67976716	AAAAAAAAAAAAAAT[-/AAGAC]AAGAATAAAAGAAGA	2186
rs150271781	snp	C/T	0.0150606	0.0854603	intron-variant	BPTF	GRCh38.p7	17:67922235	CTTTCATTTCTGTTT[C/T]CTTCTGCTGCTTCCT	2186
rs150311049	snp	C/G	0.00795532	0.062565	intron-variant	BPTF	GRCh38.p7	17:67848564	AGTAAGGCAATTTCT[C/G]TCTAAAATATGTAGG	2186
rs150320838	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67913301	GACAGGAAACATATT[A/G]ATGGCCAAAGATAGT	2186
rs150324297	snp	C/G	0.00636936	0.0560724	intron-variant	BPTF	GRCh38.p7	17:67957874	ATAAGAAATACTCTT[C/G]GTCATAGCTATGATT	2186
rs150366027	snp	A/G	0.00100498	0.0223938	synonymous-codon	BPTF	GRCh38.p7	17:67940548	GAAAAGCTTAACTTC[A/G]GCAACGTCCACTTCA	2186
rs150415468	snp	C/T	0.00398564	0.0444627	intron-variant	BPTF	GRCh38.p7	17:67839044	CAAAAATGAATCATA[C/T]GTACACATCTGATTT	2186
rs150449990	snp	A/G	4.94319e-05	0.00497127	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67866643	CTGAAGACCTGACCA[A/G]TAAGGCTCGGGGCAG	2186
rs150451704	snp	G/T	0.0248432	0.108648	intron-variant	BPTF	GRCh38.p7	17:67862825	TTGCTTTTTTTTTTT[G/T]TTTTGGCCTTTTCTA	2186
rs150468782	snp	A/G	0.00755907	0.0610114	intron-variant	BPTF	GRCh38.p7	17:67899512	TGCAGGTAGTTTTAT[A/G]CTTGATGCTGAGTTT	2186
rs150488265	snp	C/T	0.0111196	0.0737302	intron-variant, utr-variant-5-prime	BPTF	GRCh38.p7	17:67889882	CAACTGCTTTGCTAC[C/T]ACACATCCAAAGTGA	2186
rs150508482	snp	A/G	1.65781e-05	0.00287902	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67826225	GGAGGATGAGATGGA[A/G]GAGGACGACGATGAC	2186
rs150519459	snp	A/G	0.00835141	0.0640778	intron-variant	BPTF	GRCh38.p7	17:67873149	AGAGGAGTACTGTGG[A/G]TATACATGGTATTAA	2186
rs150552568	snp	G/T	0.0130921	0.0798413	intron-variant	BPTF	GRCh38.p7	17:67936341	TATTATGTGAGACAG[G/T]TAGCTACTAGGAAAG	2186
rs150569603	snp	A/G	0.00517822	0.0506191	intron-variant	BPTF	GRCh38.p7	17:67869735	ACGCCTGTAATCCCA[A/G]CATTTTGGGAGGCTG	2186
rs150592923	snp	C/T	0.00478085	0.0486577	intron-variant	BPTF	GRCh38.p7	17:67832604	TGTAAAGTATATAAT[C/T]TAGTGGTTTTTTTAG	2186
rs150628549	snp	A/G	0.000534902	0.0163452	synonymous-codon	BPTF	GRCh38.p7	17:67959828	AAAGGAAACTAAGAA[A/G]GACACAAAGCTTTAC	2186
rs150640551	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67914855	TTTAATGGGAGGAAA[C/T]ACCTTCCATTAAACA	2186
rs150644470	in-del	-/AGA	0.040671	0.13668	intron-variant	BPTF	GRCh38.p7	17:67936000	CAATGACATATCAAC[-/AGA]AGAAATTTGAAAAGT	2186
rs150646787	snp	C/G	0.021333	0.101051	intron-variant	BPTF	GRCh38.p7	17:67859269	TCTCACCTCAGCCCC[C/G]CTAGGAGCTGGGACT	2186
rs150687265	snp	A/G	0.0818113	0.184966	intron-variant	BPTF	GRCh38.p7	17:67980255	GAGGCTGAGGCAGGA[A/G]AATCATTTGAACCTG	2186
rs150690469	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67885506	GAGGCGGGAGAATCT[C/G]TTGAACCTGGGAGGT	2186
rs150691668	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67909125	CAGGCATGAGCCACC[A/G]CACCAGCCTATAGTA	2186
rs150709696	snp	A/G	0.00993419	0.0697739	intron-variant	BPTF	GRCh38.p7	17:67907100	TGATGAGGGAGGATC[A/G]TTTGAGCCCAGGAGT	2186
rs150763070	snp	C/T	0.00517822	0.0506191	intron-variant	BPTF	GRCh38.p7	17:67971919	ATGGCATTCTGTCTG[C/T]GCTATTGGAAAACAC	2186
rs150781461	snp	C/T	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67902131	CTGGCCTTGCTTCCT[C/T]CACAAAGAGAAGCCT	2186
rs150803053	snp	C/G	0.0130921	0.0798413	intron-variant	BPTF	GRCh38.p7	17:67864509	CTCCAGCCTGGGCAA[C/G]AGAGTGAGACTCCAT	2186
rs150833966	snp	C/G	0.00398564	0.0444627	intron-variant	BPTF	GRCh38.p7	17:67931388	TGAGGCAGGAGGATT[C/G]CTTAAGCCCAGGAGT	2186
rs150850537	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67882574	ATTTTAAATAGTAGT[A/G]TTTTCATAATACCAG	2186
rs150918566	snp	A/G	0.0126979	0.078662	intron-variant	BPTF	GRCh38.p7	17:67970303	GCCCGAGAGACTGAG[A/G]CAGGACGATCACTTC	2186
rs150952618	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67916639	GATGTTTGGGCGGGC[A/G]CCTGTAATCCCGGCT	2186
rs150957894	snp	C/T	0.00438332	0.0466095	intron-variant	BPTF	GRCh38.p7	17:67862016	AGTCTCACTCTGTCG[C/T]CCAGGCTGGAGTGCA	2186
rs150967978	snp	C/G	0.00557542	0.0525036	intron-variant	BPTF	GRCh38.p7	17:67927532	TTGCAGGTTTGCCAA[C/G]TTTAATAATAGTGTC	2186
rs151008626	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67888460	CCGGGCATGGTGGTG[C/T]GTGCCTGTAATCCCA	2186
rs151013310	snp	A/G	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67923350	GGCATGAGCTACCCT[A/G]CCTGGGGTAAAAGAA	2186
rs151029781	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67908010	TTACAAAAGTTTATA[C/T]ACATACTTTTTTCCT	2186
rs151077742	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67974734	GTGGAGAAGATGCAC[A/G]GGGCAATGCTGTGGG	2186
rs151082055	snp	A/G	0.000633344	0.017784	intron-variant	BPTF	GRCh38.p7	17:67904874	ATGTCCTGCATAATC[A/G]TTTCTGCTTTATATT	2186
rs151096634	snp	C/T	3.2969e-05	0.00405998	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67928401	TTGCAACTTCCACTA[C/T]TTCCCCAACAAGCAG	2186
rs151119383	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67866099	GCACTCTAGCCCGGG[C/T]GACAGAGTGAGACCC	2186
rs151169336	snp	A/C	0.0150606	0.0854603	intron-variant	BPTF	GRCh38.p7	17:67857853	GTACAGTGGCGCGAT[A/C]CTTGGCTCACTGCAA	2186
rs151177478	in-del	-/A	0.0232847	0.105357	intron-variant	BPTF	GRCh38.p7	17:67956852	CATGTAGCCCCAGCT[-/A]ACTCAGTAGGCTGAG	2186
rs151199508	snp	C/T	0.00636936	0.0560724	intron-variant	BPTF	GRCh38.p7	17:67957674	TTAGGAGTTCAGTTA[C/T]CTGAACAACACAGCA	2186
rs151219553	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67854918	TGAAGGAATATGTGC[A/G]TTAAAATAGCTTTTA	2186
rs151235085	snp	A/T	0.0142736	0.0832652	intron-variant	BPTF	GRCh38.p7	17:67947242	AATGTATTATTACCC[A/T]GCTTTACTGTGTATC	2186
rs151238945	snp	A/C	0.0111196	0.0737302	intron-variant	BPTF	GRCh38.p7	17:67876570	CAGCACTTTGGGAGG[A/C]CTAGGCGGGCAGATC	2186
rs151252240	snp	G/T	0.000209655	0.0102364	utr-variant-3-prime	BPTF	GRCh38.p7	17:67982335	GCAAGAATCTGGTTG[G/T]CTGAACTATTTTAAA	2186
rs151293045	snp	C/T	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67937719	GAGTCAAAGGAGTTA[C/T]GGTCAGAGAGGTGGA	2186
rs151318505	snp	A/G	0.000115997	0.00761478	missense	BPTF	GRCh38.p7	17:67945498	CAGTCATCAAGTGTG[A/G]GTCCAGCAGAAGCCC	2186
rs151328789	snp	A/G	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67899196	GACAAATGGCAGCCT[A/G]CCCACAAAGGCCAAA	2186
rs180671735	snp	A/G	0.00199481	0.0315187	intron-variant, utr-variant-5-prime	BPTF	GRCh38.p7	17:67889341	GATTGACTCTGAGCA[A/G]TATTGGATTGTTGGC	2186
rs180692789	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67877238	CATTCTAGTGGGCAG[C/T]AGACGGACTTAATAG	2186
rs180696440	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67831690	TGGTAGTCATGGTGG[C/G]CAAGTAGTATTCTGG	2186
rs180701415	snp	A/G	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67897282	GGAGGCGGAGGTTGC[A/G]GTGAGCCGAGATCAT	2186
rs180701731	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67849336	AAATCACCTGAAGAT[C/T]GTGAGAAACTGCAGA	2186
rs180704759	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67868762	ATAAAGATACCCGGA[G/T]AGCTGTATCCAACCT	2186
rs180715093	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67933126	GGTGTGGAGGTGGGC[A/G]CCTGTAATCCCAGCT	2186
rs180741564	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67856511	TTCTGCTCCTCATTA[A/G]CATTGTGGTACTATG	2186
rs180911281	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67970863	TTTTGCTAGTATAAA[C/T]AACATGCCACTGGAC	2186
rs180924998	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67916545	CAGTGAGCCGAGATC[A/G]CGCCATTGCACTCCA	2186
rs180948654	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67980512	TCTGGTTCAGTTTCT[A/G]AAATTGCTTTTTTAA	2186
rs180953860	snp	A/G	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67960976	TTGGAAATTATACAT[A/G]ATGTAAACAGTAGAA	2186
rs180958154	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67938599	GCATCAGTAAATGAT[A/G]CTGGAATAATTGGCT	2186
rs180972934	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67853397	TTGAGCCCATGCTTC[A/G]CTGTGGAACTCCACT	2186
rs180983226	snp	A/G	0.00438332	0.0466095	intron-variant	BPTF	GRCh38.p7	17:67835917	TGATCCGCCCACCTC[A/G]GCCTCCCAAAGTGCT	2186
rs180983724	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67872654	GAGGTTGCAGTGAGT[C/T]GAGATCACGCCACTG	2186
rs181030865	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67843302	CATAGATACATATAG[A/G]TATATATCTACATGA	2186
rs181103841	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67952327	TGGAGCGTGTAGGGC[C/T]ATCTCCGTTCACTGC	2186
rs181116245	snp	A/C	0.0123036	0.0774623	intron-variant	BPTF	GRCh38.p7	17:67927330	GTTACTTATCACACC[A/C]CTGTTGATAAGCTGT	2186
rs181127100	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67904083	GCCCAGATTGGAGTG[C/T]AGTGGCACAATCTTG	2186
rs181151674	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67970191	TGAGCTGAGATCACG[C/T]CATTGCACTCCTCCA	2186
rs181208421	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67960748	GGAATGCTTAATGCC[C/T]ACCTTAAGTGGATAC	2186
rs181236098	snp	C/T	0.00755907	0.0610114	intron-variant	BPTF	GRCh38.p7	17:67844448	GAGATGGGGTTTCAC[C/T]GTGTTAGCCAGTATG	2186
rs181250690	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67884446	TTTCTGACAAGTTCT[C/T]ACTTTGTTACCCAGG	2186
rs181260740	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67835890	CAGGATGGTCTTGAT[C/T]TCCTGACCTTGTGAT	2186
rs181262412	snp	C/T	0.00556109	0.0524368	intron-variant	BPTF	GRCh38.p7	17:67894176	ACCAGGTAAATGAAT[C/T]CTGAGCCTTGTAAAT	2186
rs181263253	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67852754	AAGTTCCAGGAGGTG[A/G]AATTACAGGGTCAAA	2186
rs181268591	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67916419	AAGTGGTGAAACCCC[A/G]TCTTTACTAAATATA	2186
rs181277748	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67872496	GGATCACCTGAGGTC[A/G]GGAGTTTGAGACCAG	2186
rs181286363	snp	A/G	0.0138799	0.0821421	intron-variant	BPTF	GRCh38.p7	17:67864991	TTTTGTATTTTTAGT[A/G]GAGACCGGGTTTCAC	2186
rs181332846	snp	A/C	0	0	intron-variant	BPTF	GRCh38.p7	17:67936809	CATAAGCATTCATTT[A/C]ATCTTCATATAAAGC	2186
rs181337874	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67827438	GCAAAAGGCTGCTTT[A/G]TACATAGTCACAATT	2186
rs181364379	snp	C/G	0.000579176	0.0170074	intron-variant	BPTF	GRCh38.p7	17:67903776	CATTGTCTTTCTATG[C/G]ATGAATTCTTAGGTT	2186
rs181384413	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67863531	CCTTGTGATCTGCCC[G/T]CCTTGGCCTCTCAAA	2186
rs181399673	snp	C/T	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67926413	TACTGCAAGCTCCGC[C/T]TCCCGGGTTCACGCC	2186
rs181422961	snp	C/T	0.00438332	0.0466095	intron-variant	BPTF	GRCh38.p7	17:67826561	TTGCAGTTTGCAGGC[C/T]ACACTCGCTCGCTCT	2186
rs181431236	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67843582	AGATATATATACAGA[A/G]GATATATATCTAGAT	2186
rs181438199	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67974571	TGGTTTTACCTGCAC[A/G]TCTGACCATCTGGCT	2186
rs181480984	snp	C/G	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67895301	TTGCACCACTGCACT[C/G]CAGCCTGGGTGACAG	2186
rs181494866	snp	A/G	0.0130921	0.0798413	intron-variant	BPTF	GRCh38.p7	17:67969394	GAGGCAGAGGTTGCT[A/G]TGAGACAAGATCGCG	2186
rs181510158	snp	A/C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67853730	ATAATTTTTTTACTT[A/C/G]TGGTTTATAATCTAA	2186
rs181573879	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67956755	GATCACGAGGTCAGG[A/G]GATCAAAACCATCCT	2186
rs181585247	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67955886	GAGGTGTGGCTCATG[G/T]CCTGTAATCCAAGCA	2186
rs181587826	snp	A/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67932544	TCTACTAAAAATATT[A/T]AAAAATTAGCTGGGC	2186
rs181599275	snp	C/T	0.00636936	0.0560724	intron-variant	BPTF	GRCh38.p7	17:67858240	ATATTTTAAGAAATA[C/T]GTGTAAAATATGTGT	2186
rs181607184	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67878219	CCATCCAGATGTTGC[C/T]AGTAGTAGCAGCTTA	2186
rs181608011	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67873512	CTTATTCACAAATAG[C/T]GTACTCTAGTTGATA	2186
rs181608784	snp	G/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67973889	TATACTAGATACAGT[G/T]AAATCTGTTCCTGTT	2186
rs181614490	snp	C/T			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67897583	GCCACAGAAAGGGAC[C/T]CACCGAGCTCCTTTT	2186
rs181614657	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67921962	GGTAAACCCAGGATG[G/T]GGGTGTTGCAGTGAG	2186
rs181619919	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67836708	TCACAGTAATCAAGA[C/G]AACAAGTAGGCAGAA	2186
rs181623856	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67916892	TACACCATAATCAAC[C/T]ACTAAGTTCATTTAA	2186
rs181630565	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67836253	TTCTTTCTACTCATG[A/G]ATATGTTCTGTAATT	2186
rs181633604	snp	A/G	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67951684	GAATATATCTTGTAT[A/G]TATTACTTTAATGTA	2186
rs181638596	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67841128	GGTCAGATAGTAAGG[C/T]CAGGCATGGTGGCTC	2186
rs181743693	snp	C/G/T	0.00318978	0.0398085	downstream-variant-500B	BPTF	GRCh38.p7	17:67984785	AGGCATGCGCCACCA[C/G/T]GCCTGGCTAATTTTG	2186
rs181793244	snp	C/T	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67910761	ACTGAGATCATGCCA[C/T]TGCACTCCAGCCTGG	2186
rs181806660	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67945110	GCACCATTACTGCTT[A/G]CTGTAGCCTTGAACT	2186
rs181842633	snp	A/T	0.00636936	0.0560724	intron-variant	BPTF	GRCh38.p7	17:67934064	AAAAGAAAAAAAAAA[A/T]AATAATTCATAGGCT	2186
rs181843607	snp	A/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67868574	CCACAGAGGGCTGAC[A/T]ATAGTGCCTTTTAAG	2186
rs181854881	snp	A/G	8.28343e-05	0.00643508	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912461	CTTGTCCAGAAAGCA[A/G]TTCAGTTAATCAGGT	2186
rs181869047	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67830672	GGGAGCAGCAGGCAC[C/T]GATAGTAAAGTGTGG	2186
rs181874076	snp	A/G	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67890047	CATACCTTAAAAATC[A/G]GGGCTGGAAATTTGT	2186
rs181877797	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67975128	GAAATGGGGACAAAA[A/G]CCAAATATATATTTC	2186
rs181881456	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67957591	AAATATTCTTATGGC[C/T]GGGTGTAAGTGGCTC	2186
rs181884520	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	BPTF	GRCh38.p7	17:67983983	TTAAACTTATGCTTA[C/T]AAACTAAAGACTAAT	2186
rs182006649	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67965755	ATTATCAAGTGATAC[A/G]GATGTACTGAAGACA	2186
rs182044971	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67980882	AACAAATTAGGCTGT[G/T]TGCAATGGTGCATGC	2186
rs182053615	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67877320	ATTTATTCAACAGCT[A/G]TTTATTGAGTGCCCT	2186
rs182055343	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67966444	GAGCAGAAATCACTT[A/G]ATATAAAATATTTCA	2186
rs182055851	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67833499	ATGTTTTTATCTGTA[C/T]GTATGTTTTCATTTC	2186
rs182059283	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67851568	GTAGGAGAGAAGATA[C/T]TAGTATAAGGCATGT	2186
rs182078424	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67848769	TTTTGTCTCAATAAC[C/T]GCCAGGTCATTCTAA	2186
rs182079710	snp	A/G	0.00438332	0.0466095	intron-variant	BPTF	GRCh38.p7	17:67921149	TGGGAAGTGGAGGTT[A/G]CAGTGAGCTGAGATC	2186
rs182097279	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67840088	TCTGTATACCATTTT[A/T]TATGGAAAAATACTG	2186
rs182099566	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67888343	CCTGTAATCCCAGCA[A/C]TTTGGGAGGCCAAGG	2186
rs182206861	snp	A/C/T	0.00279162	0.0372561	intron-variant	BPTF	GRCh38.p7	17:67964810	TCAGACCATCCTGGC[A/C/T]AACACGGTGAAACCC	2186
rs182213019	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67940010	AAATGCAGTTGGCCC[A/G]GAATATTCCAGATTC	2186
rs182217499	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67918280	TTTTCAGGTTTCTTG[C/T]TTTTGCAAAAGTTAG	2186
rs182234939	snp	A/G	1.89134e-05	0.00307512	intron-variant, utr-variant-3-prime	BPTF	GRCh38.p7	17:67982214	TGTTTTCAAAAATGA[A/G]GGGTGCTTAATTGTT	2186
rs182255249	snp	C/T	6.86589e-05	0.00585873	intron-variant	BPTF	GRCh38.p7	17:67874805	TTTTTTTGTTTGTTT[C/T]ACACATTATAGAAGA	2186
rs182261714	snp	A/G	0.0111196	0.0737302	intron-variant	BPTF	GRCh38.p7	17:67896175	CACCGTGTTAGCCAG[A/G]ATGGTCTCCATCTCC	2186
rs182301537	snp	A/G	0.00478085	0.0486577	intron-variant	BPTF	GRCh38.p7	17:67943462	AAGAGAGAGCGCCTA[A/G]AGAATTTTAAATTTC	2186
rs182311398	snp	A/G	0.00358779	0.0422022	intron-variant	BPTF	GRCh38.p7	17:67938962	GCACTGTGATACATG[A/G]TACTATTTGCAGTTG	2186
rs182336004	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67877493	CAATAGCCGTGATAG[A/T]AGACATCTTACTTGG	2186
rs182353657	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67860345	TTTTAAAGCCATGTA[A/G]AATTTTCACGCAGTT	2186
rs182361430	snp	A/T	0.00993419	0.0697739	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67897526	ACCAAGATGGTGGAA[A/T]AAAAGTCCCCAACTC	2186
rs182370239	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67844472	CAGTATGGTCTCGAT[C/T]TCCTGACCTCGTGAT	2186
rs182396150	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67856957	TCCAGCCAGTTCCCT[A/G]TTCTAGAGACACCCC	2186
rs182407543	snp	A/T	0.00716266	0.059414	intron-variant	BPTF	GRCh38.p7	17:67828177	CCTCGTGATCCGCCT[A/T]CCTCGGCCTCCCAAA	2186
rs182468304	snp	A/G	0.000395283	0.0140529	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67854367	CGTTCTTCCTTACCA[A/G]GAGGCAGAGGACTAC	2186
rs182474231	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67874109	AACAAAATTAAAAGT[A/G]ATAGTATTGCATGAT	2186
rs182480044	snp	C/T	0.0329836	0.124112	intron-variant	BPTF	GRCh38.p7	17:67895543	CACAGCTCACTGCAG[C/T]CTTGACCTCCCTGGG	2186
rs182494541	snp	A/G	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67836623	AGAGCCTCAAAATAC[A/G]TGAGGACTGATAAAA	2186
rs182550148	snp	C/T	0.0023933	0.0345097	intron-variant	BPTF	GRCh38.p7	17:67972191	CTTATATTTTTCTCT[C/T]GAGATATTTGGATTG	2186
rs182557205	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67954609	AGTTTTAGTCCTGCT[C/T]ACAGTTTTGTGTCTC	2186
rs182561316	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67929807	TGTGCTGTGCAGGCT[C/T]GCTAAGAAATCAAAT	2186
rs182597130	snp	C/T	0.00398564	0.0444627	intron-variant	BPTF	GRCh38.p7	17:67953319	TGGACTGCAATGGCG[C/T]GATCTCGGCTCCTGC	2186
rs182619462	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67879268	TGCCTCAGCCTCCCA[A/C]ATAGCTGGGATTACA	2186
rs182654893	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67841446	ATACCACTATTTAAT[A/G]CTAATATAAAATTAG	2186
rs182662495	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67904464	TGTTATAAAACTGTA[A/C]AATTGTGTTACATTT	2186
rs182667031	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67837511	CTCCTTGGTCCAAGC[A/G]GTTCCCCTGCCTCAG	2186
rs182674144	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67947688	CTAACCTGTGGTGAT[C/T]ATAAAATATGCGCTT	2186
rs182681877	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67922353	TTAGGTTTCACATCT[C/G]CACTTTATATTGGTA	2186
rs182690099	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67898596	ATTACAGGTGTGAGC[C/T]GCTGCACTTGGCCTA	2186
rs182696098	snp	C/T	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67870339	AAGAATTGAAAATTG[C/T]TGGGGAAGAGAAGGG	2186
rs182703266	snp	C/T	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67891761	ATCTTACACATACAC[C/T]AGATACGAGTTTTGG	2186
rs182707050	snp	G/T	0.0023933	0.0345097	intron-variant	BPTF	GRCh38.p7	17:67967051	GTTGCAGTGAACAGA[G/T]ATCGCGCCACTGCAC	2186
rs182858715	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67828589	GCTGGAGTGCAATGG[C/T]ACAATCTTGGCTCAC	2186
rs182861126	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67845089	AGTATACTTGTGATA[A/G]GAATGCTGTATAAGT	2186
rs182870680	snp	A/G	0.00279162	0.0372561	intron-variant	BPTF	GRCh38.p7	17:67865873	CAGAAGTAAAGAAGA[A/G]GGATGAGATATTATT	2186
rs182882531	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67886877	CATAATTCATCTACT[A/G]TTTCTCTATTAATGG	2186
rs182900524	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67854819	TAGACTAGTTTCCTT[C/T]GTGATTGATGTAGCA	2186
rs182911727	snp	A/C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67964739	GGCATGGTGGCTCAT[A/C/G]CCTGTAATCCCAGCA	2186
rs182921271	snp	A/G	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67846884	TTTTGTTATTTTAGT[A/G]GAGACAGGGTTTCGC	2186
rs182932345	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67928659	AAAAGAATTTTCAAC[C/T]CTTTAGCTACTGAAA	2186
rs182937471	snp	C/T	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67917355	GTCTCAAACTCCTGA[C/T]CTCGTGATCCCCCCA	2186
rs182949461	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67884572	AGGCATGCACTACTA[C/T]GCCTGGCTAATTTTT	2186
rs183040822	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67976951	AAGACTCACCCCTAC[A/G]TACATCGCTATAAAA	2186
rs183042909	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67923504	TTTTTTTTTTTTGAA[A/G]CAGAGTCTCGCTCTG	2186
rs183050563	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67900974	CAGTGAGCTATGATT[A/G]CGCCACTGTACTGCA	2186
rs183051923	snp	A/G	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67958126	TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA	2186
rs183057279	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67880044	TTCATTTTCTTTAAT[C/T]GCCTTTTTTTAAGGA	2186
rs183077504	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67949229	AATTAGCCAAACATG[A/G]TGGCATACGCCTGTA	2186
rs183091451	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67861554	CTCCTGACCTCAGGT[G/T]ATCAGCCCACCTCAG	2186
rs183124124	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67977189	TCATGTGAGGACTCA[G/T]GGCATCCTTTCTTGG	2186
rs183144401	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	BPTF	GRCh38.p7	17:67981609	AAAAAATTTACTCTA[A/G]CAGCCATGTTGAACA	2186
rs183201562	snp	A/G	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67907092	CAGGAGGCTGATGAG[A/G]GAGGATCGTTTGAGC	2186
rs183206854	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67828783	TCCACCTGCCTCAGC[C/T]TCCCAAAGTGCTGGG	2186
rs183207124	snp	A/G	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67939192	GAATTTTACCATGGC[A/G]TTAGTTTAACAACAA	2186
rs183219956	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67936432	AAAACTGACAGTTGT[A/G]GTAAATTGCCAGAGA	2186
rs183222584	snp	A/G	0.0023933	0.0345097	intron-variant	BPTF	GRCh38.p7	17:67866373	AGTTTTAGTGCATAA[A/G]CTTTGTTTTAAGTTT	2186
rs183308318	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67842304	GGCCACTACATCCTT[A/C]TTAAATTTCCTGTTG	2186
rs183341639	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67849988	TTCTAGGCCTATTGA[A/G]TCAGTGACATATGCA	2186
rs183345781	snp	A/G	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67869504	AGTAAAGTACCTTGC[A/G]AAAACTGTGTGAGAT	2186
rs183419216	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67913999	TCCTTTTTCATGTCC[C/T]TGTCTTTATCTTTTC	2186
rs183450639	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67958462	GCCAGGCAGTGTGGC[C/T]CACACCTGTAATCCC	2186
rs183485542	snp	A/G	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67869801	ATCCTGGCTAACATG[A/G]TGAAACCCCGTCTCT	2186
rs183522517	snp	A/G			missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912829	GTGGACATCATCTCT[A/G]TAAAGGAGCAGAGCA	2186
rs183534662	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67929280	AGCAACCGAGCACCA[C/T]GTAATGCTTTCCAAT	2186
rs183540640	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67905220	TTCTAGACTACCTGG[C/T]TAACATGGTGAAACC	2186
rs183552452	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67885819	AGTCATATCACTTGG[C/T]TATTCTCCAGCTCTG	2186
rs183554525	snp	A/C	0.0023933	0.0345097	intron-variant	BPTF	GRCh38.p7	17:67971229	GATTACAGGCATGCG[A/C]CACCACACCCAGCTA	2186
rs183593818	snp	C/T	0.00478085	0.0486577	intron-variant	BPTF	GRCh38.p7	17:67954044	CAGGCGGGAGTGCAG[C/T]GGTGCAATCACAGCA	2186
rs183642984	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67866774	ATTTGAAAATAGATT[A/G]AAATTTTCAAGTACA	2186
rs183664918	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67830079	AAATTTAGACTTACT[C/T]CAGCCTATAGGTTTT	2186
rs183679772	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67847468	GCAGTGAGCAGAGGT[A/C]GCGCCACTGCACTCC	2186
rs183699272	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67934641	AGCACATTGGGAGGC[C/T]GGCGGGTGGATCACA	2186
rs183702289	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67923592	GGCTCAAGCAATTCT[G/T]CCTCAGCCTCCTGAG	2186
rs183706477	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67967764	GCAGAGGTTGCAGTG[A/G]GCTGAGATCACGCCA	2186
rs183715207	snp	C/T	0.0228947	0.104514	intron-variant	BPTF	GRCh38.p7	17:67968605	AACACGGTGAAACCC[C/T]GTGTTAGCCCGTCTC	2186
rs183733815	snp	A/C	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67890967	ATGCAGTAGTTTTAG[A/C]ATGTATACAAATTTT	2186
rs183740018	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	BPTF	GRCh38.p7	17:67983804	AAGTTTCTTTCCTTT[C/T]AATGTTTCCCTGCTA	2186
rs183745966	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67965626	AGAATCTCTTGAACC[C/T]GGGAGGCAGAGGTTG	2186
rs183757096	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67943132	GGAGGGAATTGAAAT[A/C]CGGGTGAGTCATATG	2186
rs183760552	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67850618	GTGATCTGCCCACCT[C/T]GGACTCCCAAAGTGC	2186
rs183785693	snp	A/G	0.00636936	0.0560724	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67897465	ACTAACACAGTATTC[A/G]GGTTTCCTACATCCA	2186
rs183806861	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67923181	CCACCTCAGCCTCCC[C/T]GGTACCTAGGACTAC	2186
rs183812463	snp	C/T	0.00517822	0.0506191	intron-variant	BPTF	GRCh38.p7	17:67879492	TTTGGTTCTGGAGTT[C/T]TCACTGTGAGAAGGT	2186
rs183814374	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67974008	CAGATAAGATTATCT[C/T]ATTACTTTTCAGATA	2186
rs183822037	snp	A/G	0.000434129	0.0147267	intron-variant	BPTF	GRCh38.p7	17:67920191	ACCTGTTAACCATGT[A/G]TTTTATGAATTGAAA	2186
rs183982268	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67948445	ATAGAGTAAAAAGCA[A/G]TGCAGCGTGTGTGTC	2186
rs183998137	snp	C/G	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67860977	TTAACTTACTGACTT[C/G]CCGTGCCTGAATTCC	2186
rs184000525	snp	C/T			utr-variant-3-prime	BPTF	GRCh38.p7	17:67982657	GCTGGTTTAGAGTCT[C/T]ACAGAAAACTTTTGA	2186
rs184002261	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67899926	ATGTTTAGCACAAAA[G/T]TATTGATTGCCAGGG	2186
rs184007205	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67832196	CCCGGCCTCTAATTT[A/T]TTTCATGCTTTTGGT	2186
rs184027018	snp	A/G	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67919309	GGGAGGCCAAGGCAG[A/G]AGGATCACTTGAGGC	2186
rs184047237	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67897187	AACAAAAACAAAAAA[C/T]GAAATTAACCAGGCG	2186
rs184064707	snp	C/G	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67941487	GTATATAATACTTCA[C/G]TAATTAATATAGTGA	2186
rs184079107	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67940832	ATAAACCCCAACTAC[C/T]AGAGTAATCTTTAGA	2186
rs184080298	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67838935	TTTAAAAATTAATTT[A/T]GTATTTAGCCACCTA	2186
rs184081923	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67856344	TCCTGTTTCTGTGTC[C/T]TGGATATAGTATTTT	2186
rs184089351	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67876065	TGTACTAATGGCTCA[A/G]TGTTGAATGATCTGA	2186
rs184172433	snp	A/T	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67964833	TGAAACCCCGTCTCT[A/T]CTAAAAATACAAAAA	2186
rs184276002	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67968904	GAGAATTGCTTGAAC[C/T]TGGAAGGCAGAGGTT	2186
rs184276057	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67916458	AGCCCGGCGTGGTGG[C/T]GGGCGCCTGTAATCC	2186
rs184279787	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67949795	AGACACGGTGTCTCA[C/T]GCCTGTAATCCCAGC	2186
rs184288645	snp	C/G	0.00993419	0.0697739	intron-variant	BPTF	GRCh38.p7	17:67894621	GTGTGAGCCACCGCA[C/G]CCACCATGAATATTA	2186
rs184303411	snp	C/T	0.0150606	0.0854603	intron-variant	BPTF	GRCh38.p7	17:67978552	TCCGCCTGCCTCAGC[C/T]TCCCAAAGTGCTGGG	2186
rs184319942	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67853084	GAGGTCGCAGTGAGC[C/T]GAGGTCACGCCACCA	2186
rs184322580	snp	C/T	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67872578	AGGTGTGGTGGTATG[C/T]GCCTATAGTCTCAGC	2186
rs184327904	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67924440	TTTTTAAATTGAGAT[A/C]ATATCATACCTTTGT	2186
rs184329199	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67969595	TTTTAATGGGTTTTT[A/G]TGGTCCATTAGTTGA	2186
rs184351422	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67908191	TGTGACAGAGTCTTG[C/T]TCTGTCAGCCAGGCT	2186
rs184353642	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67877242	CTAGTGGGCAGTAGA[C/T]GGACTTAATAGAGTT	2186
rs184382277	snp	C/T	0.0275645	0.114116	intron-variant	BPTF	GRCh38.p7	17:67955060	TTTGGGAGGCCGAGG[C/T]GGGCGGATCACGAGG	2186
rs184383743	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67839664	GTAGCAGTCCCTTAT[A/G]TGAGTGTATCACAGT	2186
rs184504300	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67972624	TTTTAACATTTTTTG[A/G]AGTCATATCTATTAA	2186
rs184512730	snp	A/G			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67887632	AGGACTTTTTCAATT[A/G]CAAGTGACCAAACCA	2186
rs184520798	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67856732	GGTCTTGCTGGTGGT[A/T]TTCTGGTGGCTGAGT	2186
rs184520918	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67931251	GCCTGGGCGAAAGAG[C/T]GAGATTCTGTCTCTA	2186
rs184563601	snp	C/T	0.033485	0.124985	intron-variant	BPTF	GRCh38.p7	17:67959508	TTTACATGACTCTAA[C/T]GATAGTCTTGTATTG	2186
rs184573753	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67936572	CAAACCACTCTCTTC[C/T]CCAGGGTTTTGCCAC	2186
rs184584103	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67915413	AGATCACATTCATGG[A/G]AAGTACTTCCCTTTA	2186
rs184587228	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	BPTF	GRCh38.p7	17:67824137	CCCAGCATCTTTTTT[A/T]AAAAAAATTGAGACA	2186
rs184588374	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67863255	AACAGACACATCACT[C/T]CAGTTGCTGCCTCTA	2186
rs184593642	snp	A/G	0.00993419	0.0697739	intron-variant	BPTF	GRCh38.p7	17:67842771	CTGAGAGAAATGTCA[A/G]TCCAGAATTCTGTAT	2186
rs184608754	snp	C/T	0.0349115	0.127424	intron-variant	BPTF	GRCh38.p7	17:67977917	TGGAGTGCAATGGCG[C/T]GATCTCGGCTCACCA	2186
rs184619437	snp	C/G	0.0130921	0.0798413	upstream-variant-2KB	BPTF	GRCh38.p7	17:67825254	AAGGCCTTTGACGCC[C/G]GGCATTTCGCGAGCT	2186
rs184621433	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67871549	CTATATTTGCTTTAT[A/C]CTATGCCTGTATGGT	2186
rs184624926	snp	C/T	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67843366	GCAGTGGTGTGATGT[C/T]GGCTCATTTTTGTAT	2186
rs184630577	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67892923	TTTGAAGTATCCATG[A/G]GGTCTTACACTGTAG	2186
rs184635513	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67932615	CCGAGGTGGAAGAAT[C/T]GCTTGAAACCAGGAG	2186
rs184637593	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67965068	AAAAGGGGACTGGGC[A/G]TGGTGGCTAACACCT	2186
rs184767498	snp	A/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67956678	AAAAAAAAAAAAAAA[A/T]AACGGTCAGGCACAG	2186
rs184786520	snp	C/T	4.96438e-05	0.00498191	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67910941	ACCAATGGAAGTAGA[C/T]GATGACATGAAAACA	2186
rs184792451	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67955401	GCAAACTCTATTTCA[G/T]GTACAAATGGACCTT	2186
rs184801561	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67932312	ACAGAAAATCAAGGA[G/T]ATAGCAAAGAAACAT	2186
rs184809717	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67910398	AATTACTGGATCATA[C/T]GGTAACTCTGTTTAA	2186
rs184830336	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67973869	CTTAATATATGTGAA[A/G]TTCTTATACTAGATA	2186
rs184836631	snp	A/G	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67848044	CTATACCAATACCGA[A/G]TGAGGCCACTTTCTC	2186
rs184844843	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67867852	CTGGGTGAGGCAGTG[C/T]TCGTCAGGTTTCTCC	2186
rs184849356	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67887947	CCTTGAGGAAGGAAT[C/T]TGAGTGGCTTATCTT	2186
rs184876227	snp	A/C	0.00358779	0.0422022	intron-variant	BPTF	GRCh38.p7	17:67936860	TTTACCGATGAGAAA[A/C]TTGAAATTTAGAATG	2186
rs184907290	snp	A/C	0.0154538	0.0865337	intron-variant	BPTF	GRCh38.p7	17:67980049	AAACAAACAAACAAA[A/C]AAAAACCTACCCAGG	2186
rs184950167	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	BPTF	GRCh38.p7	17:67824564	ATAAGGTTTGAGGGT[C/G]CCTGAAATGTCATCA	2186
rs184960024	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67901469	ATTCTGAGTGGAAAA[A/G]TGTTATTGTAATCAA	2186
rs184974931	snp	A/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67863004	ACATTTTTGAGTATG[A/T]TAGCAGCAGCACCCC	2186
rs185006061	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67967202	GCTGGAGTGTACTAG[C/T]GCGATCTCACATCAC	2186
rs185057843	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67947999	AAGTTTTTGTCTCAT[C/T]TGTAGAGGCATAGAA	2186
rs185075474	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67843204	TACATCTACATACAT[C/G]TAGATGTATGTAGAT	2186
rs185138557	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67960522	ACTTGTATTTGGTGA[C/T]ATAAACAAGATTATA	2186
rs185212459	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67915980	CATTGTTTGACCACA[A/G]AGAATGAGGACAAAC	2186
rs185214474	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67871796	TGCTGAACATTTTGG[A/G]TCTCTTTTTCTTTTT	2186
rs185238686	snp	A/C	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67835119	GGAGGCTGAGGTGGG[A/C]GGATTGCTTGAGCCC	2186
rs185273809	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67966772	GGGTATAAATTGGTA[C/T]GGTCACTTTGGAGGG	2186
rs185280409	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67946660	CAGACATTATAGCAA[C/T]TCCTTTAAAGTTATT	2186
rs185286027	snp	C/G/T	0.00201589	0.0316845	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67893690	AGAAAACAACATCCC[C/G/T]TCATCCTTTCTTCAT	2186
rs185288669	snp	G/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67922122	TGTACCTGGCAGGCC[G/T]TCAGTCTCCTTGACC	2186
rs185291122	snp	A/G	0.0023933	0.0345097	intron-variant, utr-variant-5-prime	BPTF	GRCh38.p7	17:67889432	GACCCAGACCAAATG[A/G]TGTCTAAAAAGTATC	2186
rs185315471	snp	C/T	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67832046	AGGCGCCTGCCACCA[C/T]GCCCGTCTAATTTTT	2186
rs185318453	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67936750	AAAATAGCAACTGTC[A/G]TATATTCATCATTGA	2186
rs185319575	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67849401	TTCTGAATTTCTCTC[A/T]AACATGATAATGCCA	2186
rs185320491	snp	C/G	0.00438332	0.0466095	intron-variant	BPTF	GRCh38.p7	17:67852515	TTCATTGTTCTGTAG[C/G]TGTTCATTCCTTCTG	2186
rs185324846	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67859196	TGTCGCCCAGGCTAG[A/G]GTGCAGTGGCATGAT	2186
rs185333157	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67869200	TACAACAACAGAGAA[C/T]CATCTTTAGTCCTCT	2186
rs185333590	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67878704	TGTGTGTGTGTGTGT[C/G]AGTCGTTTAGATATC	2186
rs185340906	snp	A/G			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67897963	TCTGAAAATATTGGT[A/G]TGCAGATATATTCAG	2186
rs185366540	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67841165	GTAATCCCAGCACTT[C/G]GGGAGGCCAAGGCAG	2186
rs185431997	snp	A/G	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67969116	AGACCAGCCTGGACA[A/G]CATGGCAAAACCCTG	2186
rs185444071	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67882714	CCAAAGTCACTTAAA[A/G]TAATCCCCTGGGCTG	2186
rs185452643	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67926075	TGCAGTGGCACGATC[A/G]TGGCTCACCACATTC	2186
rs185462983	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67851773	ACAGTCCCAGTGGTG[G/T]TATACTGGTGTTTCC	2186
rs185543637	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67902874	TTAGGGTGTGATAAA[A/G]GCAGTTCTTCTGCCA	2186
rs185544693	snp	A/G	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67970311	GACTGAGGCAGGACG[A/G]TCACTTCAGCTGGGA	2186
rs185547504	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67978742	AGCACTCCCCAGAGG[C/G]TCAGTAGAGCAAGAA	2186
rs185577300	snp	A/G	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67950606	ACTTTGGGAGGCTGA[A/G]GCGAGCGGATCATTT	2186
rs185602518	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67952511	CAAGTGATCCTCCCT[C/T]CTCGGCCTCCCAAAG	2186
rs185636788	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67834303	GACTTTAATTTTATA[A/C]AACATTTTTAGAGGT	2186
rs185705855	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67896209	CCTTGTGATCCGCCC[A/G]CCTTGGCCTCCCAAA	2186
rs185740750	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67855259	TGAGCTGAGATCACA[C/T]CACTGCATTCCAGCC	2186
rs185743095	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67830489	TTTTCAGTATAATTT[C/G]TGATTGCTGCATGCG	2186
rs185824978	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67951985	ACTTGAACCCAGAAG[A/G]TGGAGGTTGCAGTGA	2186
rs185836858	snp	C/T	0.0023933	0.0345097	intron-variant	BPTF	GRCh38.p7	17:67926439	ACGCCATTCTCCTGC[C/T]TCAGCCTCCCGAGTA	2186
rs185848463	snp	A/G	0.00478085	0.0486577	intron-variant	BPTF	GRCh38.p7	17:67835912	CCTTGTGATCCGCCC[A/G]CCTCAGCCTCCCAAA	2186
rs185867720	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67838507	TTTGAGCTGGAGTAT[C/T]GCTCTGTCACCCAAG	2186
rs185874790	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67864388	AAAAATTAGCTGGGC[A/G]TGGTGGTGTGTGCCT	2186
rs185882012	snp	A/C	0.00315039	0.0395635	intron-variant	BPTF	GRCh38.p7	17:67875517	CCTGAAGCAATTTTA[A/C]AGAATATCTTTGAAG	2186
rs185882927	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67836292	TGGGAAACGGCATGG[A/C]CATGTGATTCATACC	2186
rs185883196	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67884162	TTTTTTTTTTTGAAA[C/T]AATCTCGTGCTGTCA	2186
rs185893058	snp	G/T	0.00438332	0.0466095	intron-variant	BPTF	GRCh38.p7	17:67903999	GAATACTTACTAATT[G/T]TATTTTTGACATAGT	2186
rs185910966	snp	C/T	0.00557542	0.0525036	intron-variant	BPTF	GRCh38.p7	17:67844270	TTTTTTTTTTTGAGA[C/T]GGAGTCTAGCTCTGT	2186
rs185918963	snp	C/G	8.26617e-05	0.00642838	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911545	GATGACTCTAAACTA[C/G]CCAGTGCAGATGATA	2186
rs185945401	snp	A/G	0.00993419	0.0697739	intron-variant	BPTF	GRCh38.p7	17:67922398	CTTCTCTGTGCGGTG[A/G]TAGGGAAACACATGT	2186
rs185947487	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67879289	TGGGATTACAGGTGC[C/T]CACCACCACGTCTGG	2186
rs185954199	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67957081	TGAGGTCCGGAGTTC[A/G]AGACCAGCCTGACCA	2186
rs186037229	snp	A/G	0.0023933	0.0345097	intron-variant	BPTF	GRCh38.p7	17:67899048	ATCTAATTAATTAAC[A/G]CATACAATTTTGTTC	2186
rs186041721	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67933209	GTTGCAGTGAGCCGA[C/G]ATTGTGCCACTGTAC	2186
rs186066144	snp	C/T	0.0023933	0.0345097	intron-variant	BPTF	GRCh38.p7	17:67974840	GAAGCTCTCCGAACC[C/T]GGTCCTTCTGGGTTT	2186
rs186230946	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67848818	GTAACATAATTACTC[C/T]GTCGAGGTAATAAGC	2186
rs186249521	snp	G/T	0.000798403	0.0199641	intron-variant, utr-variant-5-prime	BPTF	GRCh38.p7	17:67888952	CTTGTAGATTCCTAG[G/T]TTCCCAGCTAGTACT	2186
rs186285779	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67980751	AAGGGGCCACTTAGG[A/T]TGTCTTCTTGCCACG	2186
rs186292878	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67961039	AATACAAGTGTGCCT[C/T]ACTTTAAGCAAAATA	2186
rs186296364	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67938626	GGCTTATAGTTTGGG[A/G]GGAAAATAGACTTCC	2186
rs186297259	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67884597	ATTTTTGTATTTTTC[A/G]TAGTGATGGAGTTTC	2186
rs186321226	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67895033	GCAAAAAGTAAGAAC[C/T]ATTTTATCTTCTCTG	2186
rs186327689	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67865387	CTGGTGTGCCCAGGC[A/C]CTGTGGTAGATGCCT	2186
rs186338509	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67916586	CAAGAGCAAAACTCC[A/G]TCTCAAAAAAATAAT	2186
rs186341899	snp	A/G			downstream-variant-500B	BPTF	GRCh38.p7	17:67984848	GGTCAGGCTGGTCTC[A/G]AACTCCCGATCCCAG	2186
rs186354460	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67828235	GCGCCCAGCCTAGTA[C/T]GTTTTTTATAGTAAT	2186
rs186405613	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67868662	GTTCTGAGTTCTGCT[A/C]TTCTGCATACATTAT	2186
rs186426604	snp	A/G	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67840431	AAATCTTTATTTAAG[A/G]TGTTTAATTGGGTTG	2186
rs186433178	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67830909	TTCCCAGCAGCACCA[C/T]GCACAAACATGAAAC	2186
rs186470064	snp	A/G	0.00119737	0.0244387	intron-variant, utr-variant-3-prime	BPTF	GRCh38.p7	17:67981696	AAAGTCCTTTGACTT[A/G]GTCCTGGTAACTGTA	2186
rs186487939	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67957804	AAGGCTACAGCAAGC[C/T]GTGTTTATGTCACTG	2186
rs186494090	snp	C/T	0.0023933	0.0345097	intron-variant	BPTF	GRCh38.p7	17:67865016	TTTCACCGTGTTAAC[C/T]GGGATGGTCTCGATC	2186
rs186494911	snp	C/T	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67934315	CTGAGGTCAGGAGTT[C/T]GAGACTAGCCTGGCC	2186
rs186500840	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67904174	GCTGGGATTATAGGC[A/G]TGCACCACCACGCCT	2186
rs186518504	snp	C/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67827681	TGGTTAACTTGAAAA[C/G]TTTGATTTTAATAAA	2186
rs186522738	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67890190	CTGGTTTTGATAGAA[A/G]TACATCAAACTTGCT	2186
rs186537275	snp	G/T	3.3157e-05	0.00407154	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912474	CAATTCAGTTAATCA[G/T]GTAGAAGATATGGAA	2186
rs186551974	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67869642	CATTTCCTACAATGA[A/G]CATGTTATATAGTTC	2186
rs186581268	snp	A/G	0.00398564	0.0444627	intron-variant	BPTF	GRCh38.p7	17:67936499	CCTTTGTTGCATAAT[A/G]CCCTATGTAGCTGTA	2186
rs186589867	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67914697	ACTGGGAAGCACTCT[C/T]CTCTGAACTCTCCAG	2186
rs186609383	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67964762	TCCCAGCACTTTGGG[A/G]GGCCAAGGTGGGCGG	2186
rs186619673	snp	A/G	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67870455	AGGAGTGTATTGGTA[A/G]TGAATTGAGCATTCA	2186
rs186627328	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67892272	ATGGCTGATACACTT[C/T]CTTACTACATGAACA	2186
rs186642419	snp	C/T	0.0023933	0.0345097	intron-variant	BPTF	GRCh38.p7	17:67833679	GTTCAAGTGATTCTC[C/T]TGTCTCAGCCTCCTG	2186
rs186648190	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67851581	TATTAGTATAAGGCA[A/T]GTAGTGAGAATAGTG	2186
rs186698303	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67844449	AGATGGGGTTTCACC[A/G]TGTTAGCCAGTATGG	2186
rs186699165	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67917188	CCCGAGGTGGAGTGC[A/G]GTGGAGCGATCTCGG	2186
rs186705754	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67927419	TTTAAAGATTGTATT[A/G]TACTACTCTGTATAG	2186
rs186712509	snp	C/G	0.00993419	0.0697739	intron-variant	BPTF	GRCh38.p7	17:67884452	ACAAGTTCTCACTTT[C/G]TTACCCAGGCTAGAG	2186
rs186736362	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67874002	AAATGCTGGATGGAT[A/G]GATGGATGGATGGAT	2186
rs186745438	snp	A/C/T	3.47822e-05	0.00417014	intron-variant	BPTF	GRCh38.p7	17:67964413	CTTACAGGTGAGACC[A/C/T]CTCTGTGTGCAGCAT	2186
rs186801810	snp	C/G/T	0.000399281	0.0141238	utr-variant-3-prime	BPTF	GRCh38.p7	17:67982387	GTCAGGCTATCCTGA[C/G/T]AAGACTTGACCTAAA	2186
rs186806204	snp	A/G	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67964817	ATCCTGGCTAACACG[A/G]TGAAACCCCGTCTCT	2186
rs186947520	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67981340	TGCCATATTTTCCCA[C/T]TTTATGATCTCCAGC	2186
rs186958743	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67895521	GGCTGGAGTACAGTG[A/G]CGCCATCACAGCTCA	2186
rs186960690	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67938965	CTGTGATACATGATA[C/T]TATTTGCAGTTGCCT	2186
rs186983633	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67880170	TCTGGAAATTCGTTA[C/T]CTGCCCCCGTTAATC	2186
rs186986885	snp	A/G/T	0.00517997	0.0506535	intron-variant	BPTF	GRCh38.p7	17:67853810	AATCATTGCTTCTTC[A/G/T]TATTATTTTAACTTG	2186
rs186990227	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67928735	GCAAACAAGCTGTAA[C/T]GGTTGGTTTGTTACA	2186
rs187003879	snp	C/T	0.00279162	0.0372561	intron-variant	BPTF	GRCh38.p7	17:67923775	GTGAGCCACCGCGCC[C/T]GGCCCTCTCTCTTAT	2186
rs187007206	snp	A/G	0.00478085	0.0486577	intron-variant	BPTF	GRCh38.p7	17:67842966	AGAGCAACAGAAATG[A/G]TATCTGGGAAAATGT	2186
rs187011651	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67826667	AACTTTGGCAAACAC[A/G]TATCCATTGCATTCA	2186
rs187016164	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67901121	TAAAGCACATTTTGA[A/G]GCTTCAATAATTTGT	2186
rs187018730	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67970867	GCTAGTATAAACAAC[A/T]TGCCACTGGACATCT	2186
rs187024775	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67861741	TTCTTTAGCACAGAT[A/C]CCTAACTTTGTACAT	2186
rs187074163	snp	A/C	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67939555	CAACTTCATTCATTC[A/C]ATAGACATTTATTGA	2186
rs187078638	snp	C/G	0.00279162	0.0372561	intron-variant	BPTF	GRCh38.p7	17:67917902	CTGAAAGCTACACCT[C/G]CCAGGTTCACGCCGT	2186
rs187080733	snp	G/T	0.00517822	0.0506191	intron-variant	BPTF	GRCh38.p7	17:67853460	CACTGGGAACTTCGT[G/T]TCTGGTTGTTGACAG	2186
rs187105541	snp	A/G	0.000428202	0.0146259	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67854385	GGCAGAGGACTACCC[A/G]TATGGACCAGTAGAG	2186
rs187108098	snp	A/G	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67874325	GTTGTTTCCAAAAGG[A/G]CCTCTGTTTTCTCTT	2186
rs187118289	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67895651	TATTTTTTATAGACA[C/T]GGGGTCTCATTATGT	2186
rs187149684	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67837306	GGTAGATTCCTAGGA[C/T]TGGGATTGGATTGTT	2186
rs187203989	snp	A/G	4.95062e-05	0.004975	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67904830	GAATTACAGAAAGTC[A/G]TTAGAAGGAAGTAAG	2186
rs187225593	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67953378	CTCCTGCCTCAGCCT[C/T]CCAAGTAGCTGGGAT	2186
rs187236150	snp	C/T	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67873290	TGGTGAAACCCCGTC[C/T]CTACTAAAAATACAA	2186
rs187244534	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67972337	GCCACCCGGGTTCAA[C/G]CGATTCTTCCACCTC	2186
rs187260581	snp	C/T	0	0	intron-variant	BPTF	GRCh38.p7	17:67836099	TAAAAGTGTAAAAGC[C/T]GATATGCAAACTGAA	2186
rs187275058	snp	A/C	0.000399281	0.0141238	downstream-variant-500B	BPTF	GRCh38.p7	17:67984466	TGTACAAAAAGGATA[A/C]ATTTTATGGAAATCT	2186
rs187354675	snp	C/G	0.0023933	0.0345097	intron-variant	BPTF	GRCh38.p7	17:67832573	GATATAATTTATATA[C/G]TGTAAAATGTACCCT	2186
rs187356050	snp	C/G	0.00478085	0.0486577	intron-variant	BPTF	GRCh38.p7	17:67943906	GGAGGAACAGTGTTG[C/G]TTGTGGACAGATAAC	2186
rs187359243	snp	A/G	0.00993419	0.0697739	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67897528	CAAGATGGTGGAATA[A/G]AAGTCCCCAACTCAT	2186
rs187391144	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67857208	TCGCCCAGGCTGGAG[C/T]GCGAGTGCAATGGCG	2186
rs187442668	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67971533	CTTTAGGGCCGGGCA[C/T]GGTGGCTCATGCCTG	2186
rs187448667	snp	C/T	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67954514	ACACAGCATGTTAGT[C/T]TCCCTTACCCCCCAG	2186
rs187478035	snp	C/T	0.00557542	0.0525036	intron-variant	BPTF	GRCh38.p7	17:67838625	GGGACTACAGGTGCT[C/T]GCTGCCATGCCTGGC	2186
rs187482723	snp	G/T	0.0225045	0.103662	intron-variant	BPTF	GRCh38.p7	17:67886377	TTTTTTCTTTTTTTT[G/T]TGTGTGTGTGTGTGG	2186
rs187486775	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67855381	TTCCTCTATAGCCTA[A/G]CTCAGCTCATCCACC	2186
rs187498805	snp	C/T	0.000131811	0.00811715	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67929372	AAGTCCTGGGTATCA[C/T]TCCATCAAGTACAGG	2186
rs187505571	snp	A/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67906058	TATAATTTAAAAAAA[A/T]AATGAGGTTTTTTTT	2186
rs187512170	snp	A/C	0.00279162	0.0372561	intron-variant	BPTF	GRCh38.p7	17:67866122	TGAGACCCTGTCTCT[A/C]AAATAAATTTATTTT	2186
rs187527915	snp	G/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67958674	GTGGGGAGGTTGGAG[G/T]GCGCTGAGATTGTGC	2186
rs187562756	snp	A/G	0.00019899	0.00997272	intron-variant	BPTF	GRCh38.p7	17:67940401	CAAAATAATGCCAAG[A/G]GTGTATAAGCATTCA	2186
rs187569006	snp	A/G	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67918288	TTTCTTGTTTTTGCA[A/G]AAGTTAGGATTTTTC	2186
rs187578732	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67841643	CTGGGCTCAAGCAGT[C/T]CACCCACCTCACCCT	2186
rs187610664	snp	C/T	0.0023933	0.0345097	intron-variant	BPTF	GRCh38.p7	17:67877434	GGATGAGATGCCTTG[C/T]TAGAAGAATTGGGGT	2186
rs187612577	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67966034	GACACCAGCCTGAAT[A/G]ACAGAGCGAGACCCT	2186
rs187624377	snp	C/T	0.00358779	0.0422022	intron-variant	BPTF	GRCh38.p7	17:67850285	CTACTAGTTCATGTA[C/T]GTATTCATCCGTAAG	2186
rs187628802	snp	C/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67921178	TCACACCACTGCACT[C/G]CAGTCTGGGTAACAG	2186
rs187652501	snp	C/T	0.00597247	0.0543191	intron-variant	BPTF	GRCh38.p7	17:67968810	AAAAGAAAGAAAATT[C/T]AGAAAATAAATACTA	2186
rs187660485	snp	A/C	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67949449	GCGTGGTGGCAGGCA[A/C]CTGTAATCCCAGCTA	2186
rs187730437	snp	A/C	0.00597247	0.0543191	intron-variant	BPTF	GRCh38.p7	17:67973122	GCTCACGCCTGTAAT[A/C]CCAGCACTTTGGGAG	2186
rs187743790	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67931531	ATGAAAGAACATTTG[C/G]TTTCTGATCTTCCTG	2186
rs187768974	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67978016	TGTGCCACCACGCCC[A/G]GCTAATTTTGTATTT	2186
rs187777066	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67877763	AGCTGAGACTACAGG[C/T]GTGCACCACCATGCC	2186
rs187811565	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	BPTF	GRCh38.p7	17:67824282	ACAGGTGCACACCAC[C/T]ATGCCCGGCTAATTT	2186
rs187811639	snp	C/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67976957	CACCCCTACATACAT[C/G]GCTATAAAATTTCCA	2186
rs187814899	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67977257	TGGTGGCTCACGCCT[G/T]TAATCCCAGCACTTT	2186
rs187820458	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67891323	TTATAAAAAACTAAT[C/T]TAGTTGATTGTTTTA	2186
rs187829067	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67934835	CAAGATGGTGCCATC[A/G]CACTCCAGCCTGAGC	2186
rs187842556	snp	A/G	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67936706	TGAAAGTCTGCCTTA[A/G]ACGAATTAATTCTTA	2186
rs187848973	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67915436	TCCCTTTACAACCCA[A/T]CCAGTACTGGATAAA	2186
rs187853619	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67860355	ATGTAGAATTTTCAC[A/G]CAGTTTATAGTATGC	2186
rs187856077	snp	A/G	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67851194	AACGAGTTGTTTGGC[A/G]TGAGGTCCAGTCACA	2186
rs187994862	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67842487	TCTTCTTAGACCTCT[C/T]CTCTAAACTCCAGTT	2186
rs188006592	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67861090	AACTCATCGTTTCCC[C/G]CCATTACCTACTCTT	2186
rs188028111	snp	C/T	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67955202	AGAATGGCATGAACC[C/T]GGGAGGCAGAGCTTG	2186
rs188035042	snp	A/T	0.00438332	0.0466095	intron-variant	BPTF	GRCh38.p7	17:67907498	ATAGCTGGGATTACA[A/T]GTACCCGCCACCACG	2186
rs188039388	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	BPTF	GRCh38.p7	17:67823629	ACTTTATTGACTTAC[A/G]TTACTTACCTGGTCC	2186
rs188057757	snp	A/C/T	0.000399281	0.0141238	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67866597	ATTCTAGAAGAAATG[A/C/T]GTGAAGAAATCCACC	2186
rs188067928	snp	A/G	0.000198491	0.00996024	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67912888	CTCCCTGACCACCAC[A/G]GGAGGCACACTGGTT	2186
rs188071551	snp	A/C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67954930	AAGACCAGATAGTCT[A/C/G]TAGACAGAAACAGAT	2186
rs188090070	snp	C/T	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67829510	TGAGTTCTAAACTTT[C/T]AGAACATGCCCACTT	2186
rs188093955	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67870276	CTTTTTTTTTTTTTT[C/T]CGGCTAAGGTACAAC	2186
rs188096301	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67958348	AAAAGAAAAAACAGA[A/G]TACAGTAAAGAAGCT	2186
rs188119873	snp	A/C	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67833226	ATTTGAATAACACTT[A/C]ATTGTATGGCTATAC	2186
rs188153444	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67960837	GAAGCTGCTTTGGTG[A/G]TGCTATCTAAATGAT	2186
rs188195115	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67894802	AGGAATCTGATTTAC[A/C]TCTGTTTTTAAAGTT	2186
rs188214812	snp	C/T	0.00438332	0.0466095	intron-variant	BPTF	GRCh38.p7	17:67835913	CTTGTGATCCGCCCA[C/T]CTCAGCCTCCCAAAG	2186
rs188214987	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67937087	GGTAGATAATAATGA[A/G]GTAAATTAATTATAC	2186
rs188223698	snp	A/G	0.00517822	0.0506191	intron-variant	BPTF	GRCh38.p7	17:67968914	TGAACCTGGAAGGCA[A/G]AGGTTGCATTGAGCC	2186
rs188223775	snp	A/G	0.0209421	0.100162	intron-variant	BPTF	GRCh38.p7	17:67916531	GGAGGCGGAGGTTGC[A/G]GTGAGCCGAGATCGC	2186
rs188230101	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67853109	CCACCATACTCCAGC[C/G]TAGGCGACGGCTGTA	2186
rs188238107	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67872592	GCGCCTATAGTCTCA[G/T]CTACTTGGGAGGCTG	2186
rs188289639	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67919104	GTGAACCTGGGAGGC[A/G]GAGCTTACAGTGAGC	2186
rs188327453	snp	C/T	0.0337553	0.125452	intron-variant	BPTF	GRCh38.p7	17:67964883	GGGCGCCTGTAGTCC[C/T]AGCTACTCCGGAGGT	2186
rs188347156	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67886921	TAACAGTTTTTCATT[A/G]TTACAAATAGTGGTG	2186
rs188348420	snp	G/T	1.7938e-05	0.00299478	intron-variant	BPTF	GRCh38.p7	17:67875535	AATATCTTTGAAGTT[G/T]TGTTGTGCATTTTGC	2186
rs188361706	snp	G/T	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67930024	AGGAGGCTGAGGTGG[G/T]AGGATGGCTTGAGCC	2186
rs188368215	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67845818	TATAACTATGTATTT[A/C]TATAAATGTATATAA	2186
rs188378256	snp	A/G	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67846890	TATTTTAGTAGAGAC[A/G]GGGTTTCGCCATGTT	2186
rs188459578	snp	A/G	0.00358779	0.0422022	utr-variant-3-prime	BPTF	GRCh38.p7	17:67983869	GAAAGATGTTGCTAC[A/G]GTTCCCGATTCTTTC	2186
rs188461717	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67965697	ACAGTGTGAGACTCC[A/G]TCTCAGAACAAAAAG	2186
rs188472129	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67943252	GCATTTTGTGCATAA[A/T]AAATGTATTTTAGAA	2186
rs188486353	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67835237	ATTTAAGTAAAATGA[A/G]AAGTTAGTTTCTCCT	2186
rs188590337	snp	C/G	0.00953873	0.0683987	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67896618	GATAACACAATGTTA[C/G]AGTATTGTTTAGGGA	2186
rs188594445	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	BPTF	GRCh38.p7	17:67982809	TTCCTGTAGGTAAAA[A/G]TACAAGACGACCTCT	2186
rs188612339	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67854978	GCAAAATTCCATTGT[G/T]TTTTGATGCCTAGGC	2186
rs188637553	snp	A/G	0.00279162	0.0372561	intron-variant	BPTF	GRCh38.p7	17:67828633	TCCTGGGTTCAAGCA[A/G]TTCTCCTGCCTCAGC	2186
rs188695220	snp	C/T	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67965576	GTACGGTGGTGCACA[C/T]CTGTAATCCCAGCTA	2186
rs188700617	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67941879	TAAGAACCTCTGTTC[A/G]TCAAACTCACTACAG	2186
rs188727479	snp	A/C/G			intron-variant	BPTF	GRCh38.p7	17:67876133	TGTTTGCATGTGCTC[A/C/G]TGTAATATTTATAGC	2186
rs188735324	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67897234	TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCATG	2186
rs188757974	snp	C/T	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67919644	AAAGTGAGTCACTTA[C/T]GTGTGAACCAGTCTA	2186
rs188768152	snp	A/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67856386	CTGAGGCTATTAATG[A/T]CAGGTTTTTTTCTCT	2186
rs188772157	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67830914	AGCAGCACCATGCAC[A/G]AACATGAAACAGAAC	2186
rs188816165	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67973874	TATATGTGAAATTCT[C/T]ATACTAGATACAGTT	2186
rs188828047	snp	A/C	0.00358779	0.0422022	intron-variant	BPTF	GRCh38.p7	17:67948705	AAATAAGACAAATTG[A/C]ACCAGAATGAGGTGG	2186
rs188844156	snp	A/G/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67900001	CTGTTTCTTAACCTG[A/G/T]TTGCATTTTACATAT	2186
rs188865978	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67871710	TAGAATATACTTGTT[A/G]ATAGAATATGCATAT	2186
rs188867751	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67955723	TCCCAGCTACTTGGG[A/G]GGCTGAGGGAGGAGA	2186
rs188879197	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67932541	ATCTCTACTAAAAAT[A/G]TTAAAAAATTAGCTG	2186
rs188884988	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67888315	AGATCTGGGCCGGGC[G/T]CGGTGGCTCACACCT	2186
rs188886645	snp	A/T	0.0166325	0.0896639	intron-variant	BPTF	GRCh38.p7	17:67910456	TAACAAGTCATTTTT[A/T]AAAAAAAACTAGATA	2186
rs188898019	snp	C/G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67875090	CTCCAGTTTTACTTG[C/G/T]AAAATGAAAGTGAAA	2186
rs188924992	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67838017	TTTACTCACCTGTAC[A/G]GTATAGGATGGACTA	2186
rs189054314	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67969799	GAGATCCTGTCTTTA[C/T]AAAAAAACAAAAAAT	2186
rs189104782	snp	G/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67882226	TTTTTCCTCCAAGAA[G/T]TCCTGGTTCCTTTTA	2186
rs189114303	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67923418	TTGACTTTACTCCAC[C/T]TTTGATTTTAAGTGC	2186
rs189117659	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67952003	GAGGTTGCAGTGACC[C/T]GAGATCATGCCACTG	2186
rs189121322	snp	G/T	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67925977	CTCATCTCTGCAATG[G/T]AACCTAACATATTAC	2186
rs189121772	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67926594	CTCCCAAAGTGCTGG[C/G]ATTACAGGCGTGAGC	2186
rs189125559	snp	A/G	0.00874735	0.0655527	intron-variant	BPTF	GRCh38.p7	17:67884441	TTTTTTTTCTGACAA[A/G]TTCTCACTTTGTTAC	2186
rs189131512	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67904059	TTTGAGACAGAGTCT[C/T]GCTCTGTTGCCCAGA	2186
rs189135725	snp	C/T	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67866903	TACACCTAGGTTATA[C/T]GGCATAGCCTGTTGC	2186
rs189139274	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67843289	ATAGATATGTAGACA[C/T]AGATACATATAGATA	2186
rs189144607	snp	C/T	0.00557542	0.0525036	intron-variant	BPTF	GRCh38.p7	17:67967797	GCATTCCAGCCTGGA[C/T]GACAGAGCGAGACTC	2186
rs189145980	snp	A/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67887688	GAATTTAATTAGCTC[A/G]TGTAGTTGGGAAGTC	2186
rs189153016	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67892961	GATAAAAGGACCCGA[A/G]AGGATGTTTTTAGGA	2186
rs189157617	snp	A/G	0.00676609	0.0577691	intron-variant	BPTF	GRCh38.p7	17:67908858	TTTTTTTGTTGACAC[A/G]GAGTCTCACTCTGTC	2186
rs189174028	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67830265	TGAGACTTCTGAGAA[C/T]ACTTACCTGGAATTT	2186
rs189175733	snp	G/T	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67847540	AAATTATCCGGGTGT[G/T]GTGGTGGGCACCTGT	2186
rs189178552	snp	C/T	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67879559	GCTATCTTAGTCCAT[C/T]TGTGTTGCTGTAAAG	2186
rs189317862	snp	A/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67980355	CTCAAAAAGAAAAAT[A/T]CATCTACCCAGAGAA	2186
rs189362559	snp	C/T	0.00597247	0.0543191	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67897497	AAAGAAAGGGGTCCA[C/T]CTAGAAAGAGTGGAC	2186
rs189365009	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67901825	GTTTGACCCTATATC[C/T]GTCAGCATTTTCAGT	2186
rs189378346	snp	C/T	0.0023933	0.0345097	intron-variant	BPTF	GRCh38.p7	17:67863347	TGGAGTGCAGTGGCA[C/T]GATCTCGGCTCACTG	2186
rs189379672	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67852722	TTTGTACTTAAATGA[A/C]TGTGTGACTACAGGA	2186
rs189386420	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67882812	ACAAGTTCAAGACCA[G/T]CCTGCCCAACATGGC	2186
rs189399617	snp	G/T	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67950110	ATTTTAAGAAGGTGA[G/T]AAATAGACCAGGCAC	2186
rs189401338	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67903308	AACTCTGGAAACAAA[A/G]TATTCTTTAACAGTG	2186
rs189405336	snp	A/G			missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67825932	AGCTCGCCCAGGGGG[A/G]GCAGCAGTAGCCGGA	2186
rs189418528	snp	C/G	0.00318978	0.0398085	upstream-variant-2KB	BPTF	GRCh38.p7	17:67824713	TTTTCCACTGCAAAG[C/G]AGAGGTAAGTTCTTG	2186
rs189419734	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67843367	CAGTGGTGTGATGTC[A/G]GCTCATTTTTGTATT	2186
rs189429523	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67863037	TTCCCGTACCAAAAG[C/T]TGGGAGTTTTCCAGG	2186
rs189492929	snp	A/C	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67980859	GTTTGCTCAATTCTG[A/C]TTAAATAAACAAATT	2186
rs189500724	snp	G/T	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67961664	CCAGTCTGGGCAACA[G/T]AGAGAGACCCCGTCT	2186
rs189533820	snp	A/C	0.0023933	0.0345097	intron-variant, utr-variant-3-prime	BPTF	GRCh38.p7	17:67981712	GTCCTGGTAACTGTA[A/C]AGTAATTTGGTTTAC	2186
rs189573336	snp	G/T	0.000798403	0.0199641	utr-variant-3-prime, downstream-variant-500B	BPTF	GRCh38.p7	17:67983273	TTCTCCAGGACAGCA[G/T]TGGCCCCTCGTTTTA	2186
rs189588019	snp	C/T	8.3423e-05	0.00645791	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67911175	AAAGACTTCTACAAA[C/T]TCTTCAAAAAATCTC	2186
rs189599464	snp	A/G	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67964807	AGATCAGACCATCCT[A/G]GCTAACACGGTGAAA	2186
rs189602585	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67939791	AGGCTCAGGCAGGAG[A/G]ATCGCTTGAACCCAG	2186
rs189606582	snp	A/C	0.00438332	0.0466095	intron-variant	BPTF	GRCh38.p7	17:67874722	TAATTTTTCCTCTTT[A/C]ATAGCTTGTATTGAA	2186
rs189608035	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67920890	TATAAACAATAAAAA[C/T]ATTTAGGAAAAAACC	2186
rs189610240	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67917912	CACCTCCCAGGTTCA[C/T]GCCGTTCTTCTGCCT	2186
rs189612862	snp	A/C	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67896063	CGCCTCCCGGGTTCA[A/C]GCCATTCTCCTGCCT	2186
rs189627279	snp	A/G	0.00517822	0.0506191	intron-variant	BPTF	GRCh38.p7	17:67956731	CACTTTGGGAGGCCG[A/G]GGCGGGCAGATCACG	2186
rs189634981	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67877309	TCTATGCAGTTATTT[A/T]TTCAACAGCTATTTA	2186
rs189638114	snp	C/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67837396	TAAACCTTCCCTAGT[C/G]TGTGCTTATGTGTTT	2186
rs189650060	snp	C/T	0.00835141	0.0640778	intron-variant	BPTF	GRCh38.p7	17:67868715	AATTTTCCCCATTCT[C/T]CATTTGCTTAAAAAT	2186
rs189671530	snp	C/T	0.00398564	0.0444627	intron-variant	BPTF	GRCh38.p7	17:67871866	AGTCTCGCTCTGTCA[C/T]CCAGGCTGGAGTGCA	2186
rs189675538	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67844309	CTGGAGTGCAGTGGC[A/G]CAATCTCCGCTCACT	2186
rs189843271	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67966268	CCTGTTGACAGAAGC[A/G]ATTGCAATGCCAGCA	2186
rs189851804	snp	A/G	0.0023933	0.0345097	intron-variant	BPTF	GRCh38.p7	17:67932835	GACACAGGCACATGA[A/G]ATAAAGGCCATAAAA	2186
rs189859209	snp	C/T	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67967547	AAACATTGGAAATGG[C/T]GGGGTGGCTCACGCT	2186
rs189863193	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67921661	ATTAACTTGGGAGTT[C/G]TTCTTGGAGAATAAC	2186
rs189886601	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67974513	GTTGGGTACTCAGTC[C/T]CCAAGATTACCCCCT	2186
rs189905005	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67849301	TTTCAGGGCAGCTTT[C/T]CAAACTTCAGTGACC	2186
rs189917610	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67848333	AAATATTTTTTTAGT[C/T]GCTACAATAACTAAA	2186
rs189918548	snp	G/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	BPTF	GRCh38.p7	17:67889136	TGATGTAGATCTGTA[G/T]CCTGCTGCCAGGCTG	2186
rs190022981	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67933691	TCAAGGAGAAATTAA[A/T]AGGAGCATAGTAAGC	2186
rs190023148	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67832178	CAGGGGTGAGCTGCC[A/G]TACCCGGCCTCTAAT	2186
rs190030646	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67849981	GACTCTATTCTAGGC[C/T]TATTGAATCAGTGAC	2186
rs190033450	snp	A/C/G	8.23966e-05	0.00641813	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67911772	TAGTTCTGATACCGT[A/C/G]TCTATTCAGGATAGC	2186
rs190040196	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67869223	AGTCCTCTAAAAGGC[A/G]ATGTGAGATAGGATT	2186
rs190071435	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	BPTF	GRCh38.p7	17:67984870	CGATCCCAGGTGATC[C/T]GCCTGCCTCGGCCTC	2186
rs190107015	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67943951	GGGAGCTTGAACTGG[A/C]ACTCTGGATTGTTGA	2186
rs190132653	snp	C/T	0.0134861	0.0810011	intron-variant	BPTF	GRCh38.p7	17:67967014	CTGAGGCAGGAGAAT[C/T]GCTTGAACCAGGGAG	2186
rs190134809	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67947371	TAATGTTAAAAATAC[A/G]GCCTTTGGAGAAGGA	2186
rs190138481	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67860327	GTGGACTCCTCATGA[C/T]AGTTTTAAAGCCATG	2186
rs190140231	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	BPTF	GRCh38.p7	17:67984489	GGAAATCTGAAACCA[A/G]GAAGATGTTAATTTC	2186
rs190141778	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67936794	TGTATGTGTTTTGTA[C/G]ATAAGCATTCATTTA	2186
rs190142917	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67879097	TCATATCATGAGTTG[A/G]TACTAGAAGAGTTTT	2186
rs190146961	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67922217	TGTACAATTCAGGTC[C/T]TGCTTTCATTTCTGT	2186
rs190152853	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67898197	CAATGTGGTGAAACC[C/T]CATCTCTACTAAAAA	2186
rs190161405	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67897545	AGTCCCCAACTCATC[A/G]TGCCCCACCTTCCAT	2186
rs190168888	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67864853	TCTGTCACCCAGGCT[A/G]GAGTGAACTGGCGCG	2186
rs190177750	snp	A/C	0.00636936	0.0560724	intron-variant	BPTF	GRCh38.p7	17:67868518	AGAATACTGTATTTT[A/C]AATTTGAGGGTGGTT	2186
rs190179223	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67979361	AGACCAGCCTGGCCA[A/G]CATGATGAAACCCTG	2186
rs190204186	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67830503	TCTGATTGCTGCATG[C/T]GAGGTACGCAGTGCA	2186
rs190205738	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67856938	TGGTGGTTTAGGAAT[C/T]TGCTCCAGCCAGTTC	2186
rs190395033	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67950720	TGGTGGGTGCCTGTA[A/G]TCCCAGCTACTTGGG	2186
rs190401206	snp	A/G	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67857412	TGATCTGTCTGCCTC[A/G]GCCTCCCAAAGTGCT	2186
rs190402031	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67916288	GTGTTCATTTTTCCA[A/C]CTGAATGCTGTCAAT	2186
rs190409383	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67877456	AATTGGGGTGGGAGA[A/G]TTGTTAAAGGCAGAC	2186
rs190433566	snp	A/G	0.00517822	0.0506191	intron-variant	BPTF	GRCh38.p7	17:67960678	CTTTTTACAGGACCA[A/G]AAAGTCTGATTGTGC	2186
rs190439284	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67841064	ACACATCTGGGGTTC[A/G]TCTAACAACTCTCCC	2186
rs190452181	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67839695	GCATTTATCCATTCA[A/G]TAGTTGGATATTTCA	2186
rs190508483	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67834697	TAAGACATGGAGCTG[A/G]AATGGGCTTTTAATA	2186
rs190515634	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67976344	CAGGTGTGGTGACGC[A/G]CGCATGTAATCTCAG	2186
rs190531601	snp	A/G	0.0023933	0.0345097	intron-variant	BPTF	GRCh38.p7	17:67957994	TTGTACCACTAGATA[A/G]CAGAAGAGGTGTGCT	2186
rs190536770	snp	A/C	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67934569	TATACTAATAATCTT[A/C]ACTTGCTTAGAAGTA	2186
rs190642802	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67969168	TGAATCAGCCAAGGC[C/G]AGGCGCAGTGGCTCA	2186
rs190645551	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67927606	CAGTGAAACAGAAAC[A/C]TTTCACAGCTCCATT	2186
rs190655460	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67874054	AAGGACACTGGACTC[A/G]GAAAAAGTCCCCAGT	2186
rs190658628	snp	C/T	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67926410	GCTTACTGCAAGCTC[C/T]GCCTCCCGGGTTCAC	2186
rs190673971	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67970502	ATAGATCTCTAAAAC[A/G]TATTGTTGGGAAAAG	2186
rs190684107	snp	A/T	0.0898077	0.191933	intron-variant	BPTF	GRCh38.p7	17:67844460	CACCGTGTTAGCCAG[A/T]ATGGTCTCGATCTCC	2186
rs190688727	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67836594	CCTTTCTAAAGGTTT[A/G]TGAACTTATTCATAG	2186
rs190692658	snp	C/T	8.23784e-05	0.00641735	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67854000	AAGAAAAAGACATCC[C/T]GCCCCTTGAATTTCC	2186
rs190704040	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67884484	GCAATGGCGCAATCA[C/T]GGCTCACTGCAGCCT	2186
rs190712661	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67851877	AGTTATCTCATTGTG[A/G]TTTTACTTTGCCTTT	2186
rs190772649	snp	A/G	0.00279162	0.0372561	intron-variant	BPTF	GRCh38.p7	17:67971633	ACATGGCGAAACCCC[A/G]TCTCTACTAAAAATA	2186
rs190773047	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67954577	TTCCTTCTGAATCTG[A/G]AGCCTAGCAGGCCTG	2186
rs190883344	snp	A/G	0.000346789	0.0131634	synonymous-codon	BPTF	GRCh38.p7	17:67948183	AGAGAGTGTGGAGCA[A/G]AAACGTAGCAAGCAG	2186
rs190886891	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67953042	CTCGGCTCACTGCAA[A/G]CTCCGTCTCCCCGGG	2186
rs190887474	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67975084	TTATCACTCCGGAGA[C/T]TCCAACCGTGTTAGG	2186
rs190905050	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67904231	ATGGGGTTTCACCAT[A/G]TTAGCCAGGTGAGTC	2186
rs190907558	snp	C/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67899480	GAACCTTCTTTGATA[C/G]TAACAATACTGCTCT	2186
rs190940549	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67860545	AGACATATTCAGCAT[A/G]TAACTCAGAGGCCAG	2186
rs190948913	snp	C/T	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67865186	GGCACTCAAAAACTT[C/T]TGGATCTTGGAGCAT	2186
rs190976935	snp	C/T	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67828092	GCCCACCAGCACACC[C/T]GGCTAATTTTTGTAT	2186
rs190994144	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67827037	GCCAAACAAGACCCA[A/G]CCAAATTTGGTTATT	2186
rs191039027	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67885766	TATCTCAGCAAACTA[C/T]CTCTGCAATATCTGG	2186
rs191062785	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67929251	TAAAACCCTGCCACA[C/T]GTAGTTTCTCCTCAG	2186
rs191066684	snp	C/T	0.00358779	0.0422022	intron-variant	BPTF	GRCh38.p7	17:67844784	GTTTCACTCTTGTTG[C/T]CCAGGCTGGAGTGCA	2186
rs191074557	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67904925	TTGACTATATTTTAG[A/G]TAAAAACATTTTTCT	2186
rs191074955	snp	A/T	0.00358779	0.0422022	intron-variant	BPTF	GRCh38.p7	17:67865512	AGAGAGGCTGTGTCT[A/T]GTCCATGTCCACATA	2186
rs191079032	snp	G/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67938740	ATTAAAGCCAAAATT[G/T]TTAAAAAGACTAGTC	2186
rs191138574	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67958441	TTAAAAAATATATGA[A/G]AAGGGGCCAGGCAGT	2186
rs191140811	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67922761	AGTTTGCCAACCACT[C/T]TTTCATGATAGAAGA	2186
rs191148573	snp	A/G	0.00279162	0.0372561	intron-variant	BPTF	GRCh38.p7	17:67957279	CAAGAGCGAAACTCC[A/G]TCTCAAAAAAATAAA	2186
rs191164972	snp	A/G	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67829824	GACGTGACATTCCTA[A/G]CATAAGAAATAGCTC	2186
rs191178947	snp	A/G	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67846948	TCAAGTGATCCACCC[A/G]CCTTGGCCTCCCAAA	2186
rs191181482	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67841982	TGCTGTAGGAATTAC[A/G]AAATATATACCTAAA	2186
rs191184250	snp	C/T	0.00835141	0.0640778	intron-variant	BPTF	GRCh38.p7	17:67870281	TTTTTTTTTTTCGGC[C/T]AAGGTACAACATCAA	2186
rs191195844	snp	A/G	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67879461	GGTGTTATTTCTTAA[A/G]TGTTTGCTGGAGTGA	2186
rs191212027	snp	C/T	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67913590	AATAAGACATAAACA[C/T]GCCTGTAAATTTCAT	2186
rs191234202	snp	G/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67919884	GCTAGATGTTAGTGA[G/T]CCTGTTAATTAAGTC	2186
rs191254292	snp	G/T	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67841270	AAAAATTAGCCGGTC[G/T]TGGTGGCACATGCCT	2186
rs191254705	snp	G/T	0.00199481	0.0315187	utr-variant-3-prime, downstream-variant-500B	BPTF	GRCh38.p7	17:67983419	ATCTGTACATTCTGT[G/T]ATACCAGGCAAATTA	2186
rs191268917	snp	A/G	0.00874735	0.0655527	intron-variant	BPTF	GRCh38.p7	17:67965591	CCTGTAATCCCAGCT[A/G]CTAAGGAGGCTGAGG	2186
rs191271120	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67943104	GAGGATAGTGCTTAC[C/T]TCTAGGGGAGAGGGA	2186
rs191378332	snp	C/T	0.00398564	0.0444627	intron-variant	BPTF	GRCh38.p7	17:67976960	CCCTACATACATCGC[C/T]ATAAAATTTCCAAAT	2186
rs191388643	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67935516	ACCAAAAAAATTAGA[C/T]CATTATTTTGCAAGT	2186
rs191408349	snp	C/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67959420	CAACTAACTAAAACT[C/G]TCACGTTAGGCTGAA	2186
rs191410438	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67851617	TAGAGCTTTTGTTTT[C/T]AGGGGTATGTGTACT	2186
rs191420793	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67936518	TATGTAGCTGTAAGT[A/G]TGTGTTTGTCTGACA	2186
rs191424837	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67892334	AAGCCTTCTTTACAC[A/T]TATGAGTAGGCTATT	2186
rs191427126	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67914920	CTAACGTCTTAATTT[A/G]CCAAAACATATTTGA	2186
rs191434781	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67891531	TTTGCTTTTTGAGTT[A/G]TTATTATGTTTGTTA	2186
rs191442353	snp	A/G	0.00557542	0.0525036	intron-variant	BPTF	GRCh38.p7	17:67834271	ATTTCATTTTGTTCA[A/G]AGAGTATACTTTGTA	2186
rs191464867	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67890221	TAAAAAGGGAATTTT[A/G]TTGACATACACTATT	2186
rs191495222	snp	A/C	0.00358779	0.0422022	intron-variant	BPTF	GRCh38.p7	17:67850295	ATGTATGTATTCATC[A/C]GTAAGTAGTATATAA	2186
rs191712001	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67869652	AATGAGCATGTTATA[C/T]AGTTCAGTATGATTC	2186
rs191726104	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67833449	TTTCCACTTTTTGGC[C/T]ATTAGGAATAATGCT	2186
rs191731561	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	BPTF	GRCh38.p7	17:67981547	ATTGCCCCCCAAAAA[A/G]TCAGATTAGTTAATA	2186
rs191734849	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67851505	TCTAATTGTGAGCTG[C/T]AAGCAGCATGTTTTA	2186
rs191737251	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67924174	TTAGTAGAGATGGGT[C/T]GAACTCCTGATCTCA	2186
rs191746120	snp	G/T	0.0119091	0.0762411	intron-variant	BPTF	GRCh38.p7	17:67832610	GTATATAATTTAGTG[G/T]TTTTTTTAGTATATT	2186
rs191747407	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67901188	ATCCAAAAATAGACC[C/T]AAGCATGGGAATTTA	2186
rs191753498	snp	C/G	0.0333695	0.124785	intron-variant	BPTF	GRCh38.p7	17:67895542	TCACAGCTCACTGCA[C/G]CCTTGACCTCCCTGG	2186
rs191762800	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67880175	AAATTCGTTACCTGC[C/T]CCCGTTAATCGTGTT	2186
rs191766741	snp	G/T	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67968846	AATTAGCCCGGCGTG[G/T]TGGCACATGCCTATA	2186
rs191778903	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67949726	ATATATAATTTACAC[A/G]TAATTACACAGCTTT	2186
rs191883821	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67936708	AAAGTCTGCCTTAAA[C/T]GAATTAATTCTTAGT	2186
rs191920051	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67978367	TCAGTGGCACAATCT[C/T]GGCTCGCTGCAACAT	2186
rs191926324	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67960032	GTGATATTCTTACCA[C/T]TGACGCTAGTAAAGT	2186
rs191945385	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67953664	CACTGCAATCTCCAC[C/T]TCCCAGGTTGAAGCA	2186
rs191968876	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67916698	TTGAACCTGGGAGGC[A/G]AAGGTTTCAGTGAGC	2186
rs191991429	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67964574	CCAGTGCCATGAGCT[C/T]TACCATATCCCCACA	2186
rs192005500	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67917252	ATTCTTCTTTCTCAG[A/C]CTCCCAACTAGCTGG	2186
rs192011073	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67836104	GTGTAAAAGCTGATA[G/T]GCAAACTGAATTGCG	2186
rs192041611	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67842556	CACATTGTAGGAAAT[A/T]AAAAGAAAGGAGTTA	2186
rs192047957	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67900870	TAAAATTGGCCAGGC[A/G]TGGTCTTGCTTGCCT	2186
rs192050538	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67861234	TGAATCAGTTTCTCT[C/T]CATTCCCACTGTCCC	2186
rs192077995	snp	A/G			upstream-variant-2KB	BPTF	GRCh38.p7	17:67824099	CTCCCAAAGTGCTGG[A/G]ATTACAGGCGTGAGC	2186
rs192136248	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67972487	GACCTCAGGTAATCC[A/G]TCCGCCTCTGCCTTC	2186
rs192155502	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67930451	TGATCCACCTGTCTC[A/G]GCCTCCCAAAGTGCT	2186
rs192191309	snp	G/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67887337	AATGCTTTATGTATT[G/T]TTGCTATTAATCTTC	2186
rs192262813	snp	A/G			intron-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67929625	GTACTGATTTGGAAA[A/G]AAATCTGTTATATTT	2186
rs192266939	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67897147	GCCTGACGAACATGG[A/G]GAAACCCTTTCTCTA	2186
rs192269196	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67906569	ACAGAGTGATAGAAC[A/G]CTGGCAGGTCCCAAG	2186
rs192286547	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67838724	CAGTCAGTCCTTCCT[C/T]CTTGGCTTCCCAAAC	2186
rs192296560	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67855617	TGGGAAGCCTGTGGG[C/T]GAGGTCAGGAGACAG	2186
rs192303979	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67875809	TTTTGTAGTAAAAGC[C/T]GAATGTCACCTAAAA	2186
rs192329858	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67895220	TGCCTGTAGTCCCAG[G/T]TACTCGGGAGGCTGA	2186
rs192370484	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67853519	AGATCTATTGCCCCT[A/G]CTTTGTGCTGTGTAT	2186
rs192383937	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67950411	CAACGTTATTATTTA[A/G]CATTTCTGGAAGTTC	2186
rs192391666	snp	A/G	0.00755907	0.0610114	intron-variant	BPTF	GRCh38.p7	17:67977903	CTTGTTGCCCAGGCT[A/G]GAGTGCAATGGCGCG	2186
rs192424204	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67863249	TTTACAAACAGACAC[A/G]TCACTCCAGTTGCTG	2186
rs192451784	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67902078	AGCATGCTACTCTGG[G/T]ATAGGTAGCATCAGA	2186
rs192477380	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67867667	GACAGTTGGGAGGAG[G/T]AGTGGTTAGGTATTT	2186
rs192478666	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67955322	TTCCTGAGGTACTCA[C/T]GTAATGATTGTTACT	2186
rs192484621	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67887786	TTTAGGTCTACATAT[A/G]TTTATGTGTGTTAAC	2186
rs192486520	snp	A/C	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67932198	CATTTTGACATTGAC[A/C]GTAAAATAGGTTGAA	2186
rs192486780	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	BPTF	GRCh38.p7	17:67982532	CTATTGTGGCAGAAG[C/T]GAGAAAACTTTGTTT	2186
rs192488302	snp	C/T	0.0142736	0.0832652	intron-variant	BPTF	GRCh38.p7	17:67964826	AACACGGTGAAACCC[C/T]GTCTCTACTAAAAAT	2186
rs192491830	snp	G/T	0.0023933	0.0345097	intron-variant	BPTF	GRCh38.p7	17:67909503	CTGGAAATTACTTGT[G/T]TATTTTCACTAAACT	2186
rs192512422	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67830347	CTGGGAGAGTTAGTG[A/G]TTTATGTCCTCTAAG	2186
rs192516967	snp	A/G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67847784	AAATGGAATGTACTG[A/G/T]AAGAGCATAACCTTG	2186
rs192523194	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67954993	TAAAATATTTGTGAT[A/G]TGTTTAAAAGCTTTG	2186
rs192576463	snp	A/C/T	0.00120139	0.0244802	intron-variant	BPTF	GRCh38.p7	17:67866736	AAGTCTGAGCTAAAC[A/C/T]GTTGGTATGAAATCA	2186
rs192607493	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67907734	ATAAATCCCAGAAAT[C/G]ATGTTTCACCAGAAG	2186
rs192710807	snp	A/C	0.00557542	0.0525036	intron-variant	BPTF	GRCh38.p7	17:67843158	CATATAAATATATAT[A/C]TACATATATAGATAC	2186
rs192741791	snp	A/C	0.00398564	0.0444627	intron-variant	BPTF	GRCh38.p7	17:67969000	AAAATAAAAAATAAA[A/C]AAAATAAATAAAGAA	2186
rs192751860	snp	C/T	0.0111196	0.0737302	intron-variant	BPTF	GRCh38.p7	17:67926070	TGGAGTGCAGTGGCA[C/T]GATCATGGCTCACCA	2186
rs192769385	snp	A/G	0.00478085	0.0486577	intron-variant	BPTF	GRCh38.p7	17:67882512	GCTTTATCCCAATAC[A/G]GGGTATTCCTATCCT	2186
rs192812925	snp	A/C	0.00279162	0.0372561	intron-variant	BPTF	GRCh38.p7	17:67968156	TAAAACATAGCTAAA[A/C]CCTTCCAAAGGATCA	2186
rs192833459	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67852031	ATATTCTAAATACAC[C/T]TCTGTGAAGAAGTGA	2186
rs192840548	snp	A/G	0.0115144	0.0749975	intron-variant	BPTF	GRCh38.p7	17:67893155	ATAGGTACTTAATAT[A/G]TGTTAGTTTTCTTTC	2186
rs192846148	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67923459	TAGTTTAGTAAGGTC[C/T]TCTCTCTCTGTCTTT	2186
rs192866844	snp	C/T	0.0023933	0.0345097	intron-variant	BPTF	GRCh38.p7	17:67979941	AGCTACTTGGGAGGC[C/T]GAGACAGGAGAATCA	2186
rs192914061	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	BPTF	GRCh38.p7	17:67824375	CTCAAGCTATCATCC[A/G]GCCTTGGCCTCTCAA	2186
rs192922381	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67862339	AATGATGACAACTAT[A/G]TATATGATACCCATG	2186
rs192966378	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67941189	GGCATGGTGGCTTGC[G/T]CCTGTAATCCCAGCA	2186
rs192977887	snp	C/T	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67828689	ATGCAGCACCACGCC[C/T]AGCTAATTTTGTATT	2186
rs192989150	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67866342	CTGCAGGGTTTTCTT[A/G]TGAGCGCCTATATTG	2186
rs193020496	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67915501	TCTTCTTTAATCTTT[A/T]ATTTTGGTACAGCGC	2186
rs193023154	snp	A/G	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67949027	CCTTGACTTGTAAAC[A/G]ATTCTGTAGGTATTG	2186
rs193042419	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67871715	TATACTTGTTGATAG[A/G]ATATGCATATTTAGT	2186
rs193057925	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67834958	TGGCTCATACCTGTA[A/G]TCCCAATACTTTGGG	2186
rs193101452	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67875297	TTCTTTAATATTATA[C/T]CAGAGTATACACTTT	2186
rs193110328	snp	A/G	0.0142736	0.0832652	intron-variant	BPTF	GRCh38.p7	17:67838387	CTTCTTCTCTTTATC[A/G]GGAAAGTAATGTAGA	2186
rs193170976	snp	A/G	0.00517822	0.0506191	intron-variant	BPTF	GRCh38.p7	17:67964916	AGGCAGGAGAATGGC[A/G]TGAACCCGGGAGGCA	2186
rs193187543	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67886782	TTACTCAGTGATACA[C/T]GGAGAGAATCTTTTT	2186
rs193188120	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67919260	TACAGTTTTGGCCAT[A/G]TGTGGTGGCTCTCAC	2186
rs193196271	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67846368	GTTATTTGAACTTCA[C/T]TTATTGTGTGGTAGT	2186
rs193233491	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67973754	TTGGATGATACGCCC[A/G]CCTCGGCCTCCCAAA	2186
rs193243275	snp	G/T	0.0102926	0.0709955	intron-variant	BPTF	GRCh38.p7	17:67940689	TATTTTAACTTTAGA[G/T]GTGATCTTATTTATT	2186
rs193256453	snp	A/G	0.00279162	0.0372561	intron-variant	BPTF	GRCh38.p7	17:67855170	GCCAGGTGTGGTGGC[A/G]CACACCTGTAATCCC	2186
rs199557757	snp	C/T	0.00199809	0.0315445	missense	BPTF	GRCh38.p7	17:67959751	TCCCAGAAGAGGAAG[C/T]GGGAAGAGGAAAAAG	2186
rs199605359	snp	C/T	1.89777e-05	0.00308034	intron-variant	BPTF	GRCh38.p7	17:67913227	GGGAGGGAGAAAATT[C/T]TAAAAAGAATTATCT	2186
rs199611735	snp	C/T			missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67929453	CAATTAGGCCCAATA[C/T]CTCAGGCTCTGGAGG	2186
rs199613113	in-del	-/C			intron-variant	BPTF	GRCh38.p7	17:67950066	AAAAAAAAAAAAAAA[-/C]AAAAAACATTTCATA	2186
rs199613205	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67855007	GCTAGGAAATAGAAT[G/T]TTTCTAGTTGGGACT	2186
rs199613995	snp	A/G	3.29478e-05	0.00405867	synonymous-codon	BPTF	GRCh38.p7	17:67945830	TACAACCTCACAACC[A/G]ATTCCAATTCAACCA	2186
rs199614407	snp	A/G	1.97572e-05	0.00314296	intron-variant	BPTF	GRCh38.p7	17:67909553	TACTCTGGAAATAAC[A/G]TAAATTATCGTTACA	2186
rs199619781	in-del	-/TTC	0.00597247	0.0543191	intron-variant	BPTF	GRCh38.p7	17:67935090	CCAAAAATACCTCTA[-/TTC]TTAATCAAAAGTTAG	2186
rs199620903	snp	C/T	0.00358779	0.0422022	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67886878	ATAATTCATCTACTA[C/T]TTCTCTATTAATGGA	2186
rs199624872	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67979182	CTCAAAAAAAAAAAA[A/T]AAAAAAAAGGCCCTG	2186
rs199645022	snp	A/G	0.00199795	0.0315433	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67920085	TCCTTATGGCATTCG[A/G]TCTGAATATTGTATC	2186
rs199648024	snp	A/G	5.02433e-05	0.0050119	missense	BPTF	GRCh38.p7	17:67940463	AGCAAGTGATGACTC[A/G]AATCATCAGGGGGCA	2186
rs199651053	snp	A/G	1.64817e-05	0.00287064	missense, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67886202	CCTAATCTGGAAAAC[A/G]GTAACAGCAGCAGTG	2186
rs199689481	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67920561	CAAGGTAGAGATAAT[C/T]CAAGAGGCATAAAGA	2186
rs199697046	in-del	-/C			intron-variant	BPTF	GRCh38.p7	17:67884141	GCATTTTCTTTCTTT[-/C]TTTTTTTTTTTTTTT	2186
rs199723483	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67879669	GTACTGACATCTGCA[G/T]CTGGTGAGGGCCTTA	2186
rs199730055	in-del	-/AA			intron-variant	BPTF	GRCh38.p7	17:67930116	GCCAGACCTTGTCTC[-/AA]AAAAAAAAAAAAAAA	2186
rs199732667	snp	G/T	0.000710303	0.0188321	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67912915	GGTTACATCTATGAC[G/T]GTGAGCAAAGAGTAT	2186
rs199767170	in-del	-/CTGCA			intron-variant	BPTF	GRCh38.p7	17:67879664	GCATGGTACTGACAT[-/CTGCA]TCTGGTGAGGGCCTT	2186
rs199768066	snp	A/G	9.40088e-05	0.00685533	intron-variant	BPTF	GRCh38.p7	17:67959920	TTGTCTTGAAAGTTT[A/G]GCTATTAAATTGGAT	2186
rs199839467	snp	C/T	0.000656753	0.0181093	intron-variant	BPTF	GRCh38.p7	17:67947831	AGACGCAGGGTCTTG[C/T]TGTCTGTCCGTCTCT	2186
rs199847964	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67956810	CTACTAAAAATACAA[A/G]AAAATTAGCCGAGTG	2186
rs199905981	snp	C/T	0.000223839	0.0105768	intron-variant	BPTF	GRCh38.p7	17:67928621	GGAACTATCATTAAG[C/T]AAAAGATTACTTTGG	2186
rs199915594	snp	C/G	0.000116895	0.00764421	intron-variant	BPTF	GRCh38.p7	17:67875750	GATGTGCCAGGTACA[C/G]AGGGCAGCGTATCAA	2186
rs199942998	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67883281	AGATCACGCCACTGC[A/C]CTTCAGCCTGGGCGA	2186
rs199969212	snp	C/G	0.00053024	0.0162739	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911465	TAGAAGAAAAAGTCT[C/G]TGACCTTGCCAGTAG	2186
rs199977152	in-del	-/A	0.0248432	0.108648	intron-variant	BPTF	GRCh38.p7	17:67951307	AGCATTAAAAAAAAA[-/A]TCTTATTTTGCAGAT	2186
rs199978431	snp	A/G/T	1.6797e-05	0.00289797	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912202	AATGTTGAACCAAAG[A/G/T]TTAATAATATAAATA	2186
rs199985944	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67913358	AAAATTGGCCAACTA[A/G]TGTACTAAAGTTTTT	2186
rs199988178	snp	C/G	1.65403e-05	0.00287574	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67874969	CAGTCCCTTGAAAAA[C/G]ACAGTGACGACAAAA	2186
rs199996143	snp	A/G	6.59174e-05	0.00574059	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911698	ACACCTCTGTCAAGA[A/G]CAATGGACTTTGAAG	2186
rs200002880	in-del	-/A			intron-variant	BPTF	GRCh38.p7	17:67980045	TGAAAACAAACAAAC[-/A]AAAAAAAAACCTACC	2186
rs200010422	snp	A/G	0.000164777	0.00907532	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67866642	ACTGAAGACCTGACC[A/G]ATAAGGCTCGGGGCA	2186
rs200025844	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67834130	ACCATTCCCTTTACC[C/G]CCAGGTGGGGCTAAG	2186
rs200043523	in-del	-/CA	0.0103295	0.0711199	intron-variant	BPTF	GRCh38.p7	17:67853647	TGTTCTGACACTGTT[-/CA]ATTTTTTAATCATGA	2186
rs200065139	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67976083	TCTTTAAAAAAAAAA[A/T]AAATAAATCAAGACT	2186
rs200072247	snp	A/G			missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67928544	GTAACATTCCAACAA[A/G]ACAAGAACTTTCATC	2186
rs200077810	snp	A/G	0.000395942	0.0140646	intron-variant	BPTF	GRCh38.p7	17:67966545	AGTGTTTTCACTGAC[A/G]ATAATGATGCTGCTT	2186
rs200097392	snp	A/T	1.65685e-05	0.00287819	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67826287	ACGACGACGCCAGTT[A/T]CTGCACGGAAAGCAG	2186
rs200111592	snp	A/G	1.64895e-05	0.00287132	synonymous-codon	BPTF	GRCh38.p7	17:67940617	ACAAGGACAAGTGAA[A/G]CTCACCATGGCTCAA	2186
rs200136899	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67940068	ATTAATTTTTTATTA[A/G]ATTAGCACTTATTTT	2186
rs200138172	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67973190	CCATCCTGGCTAACA[C/T]GGTGAAACCCCGTCT	2186
rs200147350	snp	A/G	0.000481476	0.0155083	intron-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67918857	AGGGGGAAGGGAGTT[A/G]TTTTCTAATTTAAGT	2186
rs200157452	in-del	-/G	0.163019	0.234381	intron-variant	BPTF	GRCh38.p7	17:67858619	TGGAAATTCAGTGAT[-/G]GCTGCCTGTCAGGGA	2186
rs200169476	snp	A/G	1.64879e-05	0.00287118	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911816	TGATTGTTCAGAATA[A/G]CAATGAAAGCATTTC	2186
rs200170741	snp	A/G	0.000197915	0.00994578	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67866678	AAATCCTTTCTGGCG[A/G]CAGCTAATGGTGAGA	2186
rs200179945	snp	C/G/T			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67896469	GAGTAACTAGAAACT[C/G/T]TCCCCCCAGTGCACA	2186
rs200180767	snp	A/G	8.24368e-05	0.00641963	missense	BPTF	GRCh38.p7	17:67940538	CACCTGGGCAGAAAA[A/G]CTTAACTTCAGCAAC	2186
rs200200542	snp	A/G	3.32049e-05	0.00407448	synonymous-codon	BPTF	GRCh38.p7	17:67945503	ATCAAGTGTGGGTCC[A/G]GCAGAAGCCCAGCCA	2186
rs200204370	snp	A/C/G	3.30826e-05	0.00406699	missense, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67875618	GGCGACAACACAACA[A/C/G]ATGCAACTTCAGAAG	2186
rs200208277	in-del	-/TGTCCCC			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67896468	TGAGTAACTAGAAAC[-/TGTCCCC]CCAGTGCACATAGAC	2186
rs200215613	in-del	-/TTTC			intron-variant	BPTF	GRCh38.p7	17:67879151	CTTTTTTTTTTTTTT[-/TTTC]TTTTTGAGATGGAGT	2186
rs200255198	in-del	-/AT			intron-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67919217	ATAATAATAATAATA[-/AT]AAAATATAATGCTTG	2186
rs200256041	in-del	-/C	0.0111196	0.0737302	intron-variant	BPTF	GRCh38.p7	17:67869058	TCTCCGTCTTACTCT[-/C]CCCCCCATATAGATC	2186
rs200306895	in-del	-/TTA			intron-variant	BPTF	GRCh38.p7	17:67839334	TTCCTAAGTTTTTTT[-/TTA]AAAAAAAATCAGCTA	2186
rs200317131	in-del	-/G			intron-variant	BPTF	GRCh38.p7	17:67886432	AGTTTTTAATTTTTT[-/G]AAATGAAAGTTTGGT	2186
rs200323408	in-del	-/TTTTTGAAGATG			intron-variant	BPTF	GRCh38.p7	17:67898672	AAGTCTTTTTTTTTT[-/TTTTTGAAGATG]TATTGCAAACCAAAT	2186
rs200325810	in-del	-/TGT			intron-variant	BPTF	GRCh38.p7	17:67944923	CAGGGGACAGCCAAG[-/TGT]AAGCAGGGCCCAGGC	2186
rs200355165	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67961399	TTGTCCCAAACTAGG[C/T]TGGTTTGGGAATCCA	2186
rs200357816	snp	A/T	3.33034e-05	0.00408051	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67912687	CACAGAATCAAAAAC[A/T]GTGATCAAGGTAGAA	2186
rs200378255	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67879154	TTTTTTTTTTTTTTT[C/T]TTTTTGAGATGGAGT	2186
rs200394960	snp	G/T			missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67904750	ACAGGATATGGTGGT[G/T]GGAGCTGGATTAGTA	2186
rs200425015	snp	G/T	1.70641e-05	0.00292092	synonymous-codon	BPTF	GRCh38.p7	17:67945527	CCAGCCACAGACTGC[G/T]CAGCCTTCAGCTCAG	2186
rs200451743	snp	C/T	0.00199793	0.0315432	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67920118	GAAAATCATTTGTCC[C/T]ATTGGAGTTCCAGAA	2186
rs200460709	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67967158	TTTTTTTCTTTTTTT[A/T]ATGAGACGATGTCTT	2186
rs200465104	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67973246	AGGCATGGTGGCAGA[A/T]GCCTGTAGTCCTAGC	2186
rs200471908	in-del	-/T	0.492287	0.0616198	intron-variant	BPTF	GRCh38.p7	17:67884139	TGGGCATTTTCTTTC[-/T]TTTTTTTTTTTTTTT	2186
rs200480162	snp	A/G	3.2962e-05	0.00405954	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911770	AATAGTTCTGATACC[A/G]TGTCTATTCAGGATA	2186
rs200480303	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67968057	AAAAAATGGTAATAG[C/G]AGCCACGAGTAATCG	2186
rs200489786	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67860062	TGCTTTAAAAGCTAT[C/G]GTCGTCATTCAAATT	2186
rs200495309	snp	A/T	0.000399281	0.0141238	missense	BPTF	GRCh38.p7	17:67959590	AAAAAGACCTGATGC[A/T]GTTGGCTCAGGCCAC	2186
rs200497111	snp	G/T	0.00010022	0.00707815	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911197	AAAAATCTCTCTGAA[G/T]CACCAGTAATAACGA	2186
rs200499768	snp	A/G	0.000124981	0.00790411	intron-variant	BPTF	GRCh38.p7	17:67945383	GTTCCAGAGTAATAG[A/G]AATGGTTCATCTTTC	2186
rs200511450	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67969561	TTTTCCTATGTAAAT[A/C]TTCTTCGAAAACCCA	2186
rs200521302	in-del	-/T			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67886816	TATGAATTGAATTCA[-/T]TTTTTTTTTAAAGCT	2186
rs200523890	in-del	-/AAGAAT	0.0372196	0.131242	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67897990	TCAGGAGTAAATTTA[-/AAGAAT]AAGAAACCATGGCTG	2186
rs200529597	in-del	-/G			intron-variant	BPTF	GRCh38.p7	17:67844693	GGGGTGAACCACTGC[-/G]TCCAGTCTGTTGCCT	2186
rs200578093	snp	C/T	0.00108753	0.0232934	intron-variant	BPTF	GRCh38.p7	17:67918706	GATTTCTTTGGTTTT[C/T]CTTTCAGGTATAGAC	2186
rs200595745	in-del	-/AATAATAAT	0.446902	0.154045	intron-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67919174	GAGACTCTGTCTCAA[-/AATAATAAT]AATAATAATAATAAT	2186
rs200596839	snp	A/C/G	0.000181276	0.00951877	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67866652	TGACCAATAAGGCTC[A/C/G]GGGCAGTAACAAATC	2186
rs200597847	in-del	-/G			intron-variant	BPTF	GRCh38.p7	17:67835625	TAGGGTGAAGAGGAA[-/G]TTAACATGTGATTAG	2186
rs200623895	snp	A/T	1.64781e-05	0.00287033	missense	BPTF	GRCh38.p7	17:67931963	TGATTAGAACACCAC[A/T]CCAACAGTCAACACT	2186
rs200645527	snp	A/C			missense	BPTF	GRCh38.p7	17:67959788	GCTCAAAGTCCAAGA[A/C]AAAGAAAATGATCTC	2186
rs200697649	snp	A/C	6.59163e-05	0.00574054	missense	BPTF	GRCh38.p7	17:67940588	TCTTCAGCCTCACAA[A/C]CCCCTCGCCCCCAAC	2186
rs200707619	in-del	-/AGACAT			intron-variant	BPTF	GRCh38.p7	17:67949681	TATATATATACACAC[-/AGACAT]ACATATATATATACA	2186
rs200727803	snp	A/G	0.000709682	0.0188239	intron-variant	BPTF	GRCh38.p7	17:67903946	ACAACCCTTTAAAAT[A/G]GTGTTAGCCATTTCT	2186
rs200778402	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67968786	GAGCGAGACACGTCT[A/C]AAAAAAAAAAAAGAA	2186
rs200785261	in-del	-/CAGAGATA			intron-variant	BPTF	GRCh38.p7	17:67842942	GAAATACTAGAACTT[-/CAGAGATA]AAGAGCAACAGAAAT	2186
rs200808758	snp	A/G	0.000115353	0.00759362	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911701	CCTCTGTCAAGAGCA[A/G]TGGACTTTGAAGGAA	2186
rs200808864	snp	G/T	1.87876e-05	0.00306488	intron-variant	BPTF	GRCh38.p7	17:67959528	GTCTTGTATTGTCTT[G/T]AATTGATAACAGGAA	2186
rs200828802	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67835627	GGGTGAAGAGGAAGT[A/T]AACATGTGATTAGAA	2186
rs200845949	snp	C/T	0.00199792	0.0315431	missense	BPTF	GRCh38.p7	17:67931932	ACAGGGCCTCAGATT[C/T]GCCCTGGTATGACCG	2186
rs200853934	snp	A/G	6.58957e-05	0.00573964	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67854353	AAGGAGTACCATCAC[A/G]TTCTTCCTTACCAAG	2186
rs200866212	snp	A/G	1.75357e-05	0.002961	missense, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67875556	TGCATTTTGCTGTAG[A/G]GCCAACAGAAGTTGG	2186
rs200868858	in-del	-/AT			intron-variant	BPTF	GRCh38.p7	17:67910810	ATCTCAAAAAAAAAA[-/AT]ATATATATATAAATT	2186
rs200869810	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67955447	CTTGAAATTTTGGCA[A/G]GGGGGAATCAGGTTT	2186
rs200878469	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67870766	GAAAATGCTTCATTT[C/T]TTTTTTTTTTTTTTT	2186
rs200895790	snp	A/T	1.66988e-05	0.00288949	synonymous-codon	BPTF	GRCh38.p7	17:67945638	TTCATCCCATGTCCC[A/T]TCTGAAGCACAACCC	2186
rs200912978	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67973207	GTGAAACCCCGTCTC[C/T]ACTAAAAATACAAAA	2186
rs200922480	in-del	-/CC			upstream-variant-2KB	BPTF	GRCh38.p7	17:67824220	TGCAACATCCACCTC[-/CC]AGGCTCAAGCAATCC	2186
rs200938020	in-del	-/TTTG	0.00875779	0.0655911	intron-variant	BPTF	GRCh38.p7	17:67850369	TTGCCTCATGGTGTT[-/TTTG]TTTGTTTGTTTGTTT	2186
rs200947015	snp	G/T	0.000352528	0.0132718	intron-variant	BPTF	GRCh38.p7	17:67875552	GTTGTGCATTTTGCT[G/T]TAGAGCCAACAGAAG	2186
rs200967031	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67971270	TTTTGGTAGAATCAG[G/T]GTTTCACCATGTTGG	2186
rs200989774	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67967150	GCATACTTTTTTTTT[C/T]TTTTTTTAATGAGAC	2186
rs201013403	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67903068	GTTGTGGCCGATGCC[C/T]GTGTCTCATGATTTA	2186
rs201030912	snp	C/T	1.66916e-05	0.00288886	synonymous-codon	BPTF	GRCh38.p7	17:67940653	TCAGTTAACACAGGG[C/T]CACGTAAGTAACATA	2186
rs201036890	snp	C/G	1.64781e-05	0.00287033	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67928429	CAGTACAACCAGCAC[C/G]ATCTCTCCAGCACAG	2186
rs201046289	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67937260	CAGGAGTTCAAGACC[A/G]GCCTGGCCAACATGG	2186
rs201049130	in-del	-/C	0.0283406	0.115616	intron-variant	BPTF	GRCh38.p7	17:67958298	GACTGTGCCACTGCA[-/C]TCTAGCCTGGGTGAC	2186
rs201062114	snp	C/T			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67896470	AGTAACTAGAAACTG[C/T]CCCCCCAGTGCACAT	2186
rs201069853	snp	A/G	8.23689e-05	0.00641698	intron-variant, missense	BPTF	GRCh38.p7	17:67946141	TCCAAATTCAGCAAA[A/G]CAGTGCTGTGCAGAC	2186
rs201077943	in-del	-/TTT			intron-variant	BPTF	GRCh38.p7	17:67978316	ATATATATTTTTTTT[-/TTT]GAGACAGAGTCTCAC	2186
rs201085488	snp	A/C	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67848600	TTTTTTTTAAAATTA[A/C]AAATATGAGAAATTA	2186
rs201101422	snp	A/G	0.00279162	0.0372561	intron-variant	BPTF	GRCh38.p7	17:67832047	GGCGCCTGCCACCAC[A/G]CCCGTCTAATTTTTG	2186
rs201124681	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67954173	TGGCTAATTTTGGGG[-/T]GTTTTTTGTTGTTAT	2186
rs201148602	in-del	-/T	0.368324	0.220226	intron-variant	BPTF	GRCh38.p7	17:67961470	TTCCAGAACACAGCC[-/T]TATCACCCTGTGGAG	2186
rs201157750	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67852468	CTTGCCCTCCTTTTT[A/T]TTTTTAGTTTATTTA	2186
rs201173181	snp	A/C/T	1.67598e-05	0.00289476	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912196	AGTGGTAATGTTGAA[A/C/T]CAAAGGTTAATAATA	2186
rs201187631	snp	C/T	0.000399281	0.0141238	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67854146	GACTTTTGTGCAGCT[C/T]TGGTGAGCCAAGAGC	2186
rs201199224	snp	A/G	9.9985e-05	0.00706983	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912634	TCTAAAAGAAAAACC[A/G]TCATCACAGAAGTCA	2186
rs201201162	in-del	-/G	0.0146672	0.084371	intron-variant	BPTF	GRCh38.p7	17:67952114	TTGAGTTTGAGACCA[-/G]CCTGTCCAACATGGT	2186
rs201207814	snp	A/G	0.0004302	0.01466	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911086	CTTCTTGAAAGGAGA[A/G]TTAAACAGTTTACAC	2186
rs201220445	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67960346	TATTTTAAGCAGTTG[G/T]TTTTTTTTGTATTAA	2186
rs201238468	in-del	-/A			intron-variant	BPTF	GRCh38.p7	17:67933566	GAGCACGACCTGTTT[-/A]AAAAAAAAAGAAAAA	2186
rs201246658	snp	A/C	0.0229554	0.104646	intron-variant	BPTF	GRCh38.p7	17:67932056	TCATTTTACATCTCA[A/C]CAGCCAGTCTAGGAA	2186
rs201250221	in-del	-/TGTCAGTCTTTAGTATCAGGAATATTT			intron-variant	BPTF	GRCh38.p7	17:67879023	TTTCTTCTCTGATAA[-/TGTCAGTCTTTAGTATCAGGAATATTT]TGTCAGTCTTTAGTA	2186
rs201259416	in-del	-/A			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67897165	ACCCTTTCTCTACTT[-/A]AAAAAAAACAAAAAC	2186
rs201283095	in-del	-/TGG			intron-variant	BPTF	GRCh38.p7	17:67913355	TCAAAATTGGCCAAC[-/TGG]TAATGTACTAAAGTT	2186
rs201296713	snp	A/G	0.000798403	0.0199641	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67912900	CACGGGAGGCACACT[A/G]GTTACATCTATGACT	2186
rs201333688	snp	A/C/G	0.000917304	0.0213968	intron-variant	BPTF	GRCh38.p7	17:67975994	TTCTGAATTAATTCA[A/C/G]CTCTTCACACTCTTT	2186
rs201343822	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67886426	GTTTTTTAGTTTTTA[A/T]TTTTTTAAATGAAAG	2186
rs201397814	in-del	-/AAAAAAAT			intron-variant	BPTF	GRCh38.p7	17:67957284	GCGAAACTCCGTCTC[-/AAAAAAAT]AAAAAAATAAAAAAA	2186
rs201429797	snp	A/G	1.64996e-05	0.0028722	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67903891	GCAAGCGACATGGGT[A/G]AAATACACATTTCCA	2186
rs201474291	snp	A/G			synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67928600	AGGCCAGTCAAATTC[A/G]GGTATGGAACTATCA	2186
rs201479457	snp	C/T	1.65176e-05	0.00287376	synonymous-codon	BPTF	GRCh38.p7	17:67959768	GGAAGAGGAAAAAGA[C/T]TCCAGCTCAAAGTCC	2186
rs201480742	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67969562	TTTCCTATGTAAATC[A/T]TCTTCGAAAACCCAT	2186
rs201512564	in-del	-/T/TC			intron-variant	BPTF	GRCh38.p7	17:67884140	GGCATTTTCTTTCTT[-/T/TC]TTTTTTTTTTTTTTT	2186
rs201523219	snp	A/G	0.000115453	0.00759693	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911605	CCGCTCATACAGGAG[A/G]AAAGTGACACCATTG	2186
rs201539436	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67883456	GCATTTACATTATTA[-/T]AAATTGAAAACTATG	2186
rs201540873	snp	A/C	3.31829e-05	0.00407313	intron-variant	BPTF	GRCh38.p7	17:67918670	TGTGTATGTGTATGT[A/C]TATACATATAGATAT	2186
rs201541445	in-del	-/A			intron-variant	BPTF	GRCh38.p7	17:67978308	TATATATATATATAT[-/A]TTTTTTTTGAGACAG	2186
rs201553564	snp	C/T			missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67928592	GTTAAGCAAGGCCAG[C/T]CAAATTCAGGTATGG	2186
rs201565400	in-del	-/AAAT			intron-variant	BPTF	GRCh38.p7	17:67927273	CTGCCACCAGGTTTG[-/AAAT]AAATTTCACCTGTTG	2186
rs201593313	in-del	-/A			intron-variant	BPTF	GRCh38.p7	17:67836952	TTTCTGATCCTCTGT[-/A]AACTTGGAAGATTAC	2186
rs201605152	in-del	-/TG			intron-variant	BPTF	GRCh38.p7	17:67829123	GTTTTTTGTTGTTGT[-/TG]TTTTTTCTAATTGGT	2186
rs201618328	snp	A/G	0.000399281	0.0141238	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912365	GTTCTTCAGATGCTG[A/G]AGGTAACTACCGAGA	2186
rs201658052	snp	C/G	3.29462e-05	0.00405857	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67854116	GTTTTGAGATTATCT[C/G]CTTTTCGCTTTGAGG	2186
rs201677064	snp	G/T			synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67904749	GACAGGATATGGTGG[G/T]TGGAGCTGGATTAGT	2186
rs201716234	snp	A/G	0.000667368	0.0182548	intron-variant	BPTF	GRCh38.p7	17:67928612	TTCAGGTATGGAACT[A/G]TCATTAAGTAAAAGA	2186
rs201720584	snp	A/G	6.61857e-05	0.00575226	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67910942	CCAATGGAAGTAGAC[A/G]ATGACATGAAAACAG	2186
rs201734103	snp	A/T	0.45645	0.140991	intron-variant	BPTF	GRCh38.p7	17:67978304	AATATATATATATAT[A/T]TATATTTTTTTTGAG	2186
rs201735088	snp	A/G			missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912008	GACCAGTTAATAAAT[A/G]TAGTGATCAAATAAA	2186
rs201740863	in-del	-/T	0.0232847	0.105357	intron-variant	BPTF	GRCh38.p7	17:67951008	GAGGGTGTTTCACCA[-/T]TTTTTTGTCAGGCTG	2186
rs201743826	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67976082	ATCTTTAAAAAAAAA[A/T]TAAATAAATCAAGAC	2186
rs201745424	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67973260	ATGCCTGTAGTCCTA[A/G]CTACTCCAGAGGCTG	2186
rs201773125	snp	A/G			missense	BPTF	GRCh38.p7	17:67964361	TCACGCCACTAACAG[A/G]GAAGGATTATGAGGG	2186
rs201775041	snp	A/G	0.000247368	0.0111186	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67929338	ATCTTTTTTTAAGGC[A/G]TTGTTCAAGTACAGC	2186
rs201783868	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67977823	CACTCCAGCTTGGGC[A/G]ACAGAGGGAGATTCC	2186
rs201802525	in-del	-/A			intron-variant	BPTF	GRCh38.p7	17:67965902	CCTCTACAAAACATT[-/A]AAAAAAAAATGAGCT	2186
rs201802708	snp	A/C	6.61427e-05	0.00575039	intron-variant	BPTF	GRCh38.p7	17:67948321	GGTAAGAGGGCACAT[A/C]CTTTTCTTCTGTGTC	2186
rs201807939	snp	C/G/T	1.658e-05	0.00287919	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911474	AAGTCTCTGACCTTG[C/G/T]CAGTAGAGGCCAGGA	2186
rs201824216	in-del	-/CT			intron-variant	BPTF	GRCh38.p7	17:67843226	TATGTAGATATATAC[-/CT]ATATATCTACATACA	2186
rs201847622	snp	C/T	3.30518e-05	0.00406507	synonymous-codon	BPTF	GRCh38.p7	17:67940500	CTCCACTGCAGTCTC[C/T]GCCCCTAACACGGTT	2186
rs201852272	in-del	-/AC			intron-variant, utr-variant-3-prime	BPTF	GRCh38.p7	17:67982207	CATCATTGTTTTCAA[-/AC]AAATGAAGGGTGCTT	2186
rs201856983	snp	G/T	1.64735e-05	0.00286993	intron-variant, missense	BPTF	GRCh38.p7	17:67945989	GCTACAAATACAGCA[G/T]CCACAGCCCCAAGTC	2186
rs201859733	in-del	-/G			intron-variant	BPTF	GRCh38.p7	17:67881494	CCATAATCAAGGTTT[-/G]TTTTTTTTTTTTTTT	2186
rs201866245	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67960344	TTTATTTTAAGCAGT[-/T]GTTTTTTTTTGTATT	2186
rs201872699	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67864868	AGAGTGAACTGGCGC[A/G]AACTCGGCTCACTCT	2186
rs201874143	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67858858	ACTGCCTCTTTCTTT[C/G]CCTGTGCTGCCCTTT	2186
rs201964972	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67836375	TCTTGCTCGATTTCA[C/G]TATGTTCATAGTGCC	2186
rs201967190	in-del	-/AATAAT			intron-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67919174	GAGACTCTGTCTCAA[-/AATAAT]AATAATAATAATAAT	2186
rs201969491	snp	C/T			missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67928578	CCTTTGCTACATGGG[C/T]TAAGCAAGGCCAGTC	2186
rs201979188	in-del	-/AGTGCTG			intron-variant	BPTF	GRCh38.p7	17:67871033	GCCTCGGCCTCCCAA[-/AGTGCTG]GGATTACAGGCGTGA	2186
rs201995488	snp	C/T	1.6483e-05	0.00287076	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67894040	GAAATACAGGGCAAA[C/T]TGGATCAAGGCAGTT	2186
rs201999330	snp	A/G	0.000399281	0.0141238	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67922840	ATTTCCTTTCCAAAG[A/G]AACGCCTACACCTCA	2186
rs202012993	in-del	-/CACTG			intron-variant	BPTF	GRCh38.p7	17:67930485	ATTACAGGCCTGAGC[-/CACTG]CACCTGGCCCAGATA	2186
rs202018410	snp	C/T	0.00199806	0.0315443	intron-variant	BPTF	GRCh38.p7	17:67945369	AACCACAGTTTTATG[C/T]TCCAGAGTAATAGAA	2186
rs202034310	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67841323	CTGAGGCAGGAGAAT[G/T]GCTTGAACCCAGGAG	2186
rs202042299	snp	C/G	0.00185759	0.0304195	intron-variant	BPTF	GRCh38.p7	17:67909810	GGTGATAAGAATGCA[C/G]TGGATCAGGGTCCCA	2186
rs202052488	snp	A/G	0.00199794	0.0315433	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67912087	AAAGAAAGGACAGAG[A/G]ACAAGTACATTTCAA	2186
rs202089667	in-del	-/A			intron-variant	BPTF	GRCh38.p7	17:67910455	TAACAAGTCATTTTT[-/A]AAAAAAAAACTAGAT	2186
rs202094354	snp	C/T	0.00056644	0.0168196	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67912633	ATCTAAAAGAAAAAC[C/T]GTCATCACAGAAGTC	2186
rs202095865	snp	C/T	0.000115872	0.00761069	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912860	AAACCGTGGTCACCA[C/T]GACAGTGACAGACTC	2186
rs202105424	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67832253	CAGCATGTTTCTTAA[-/T]TTAAAAAAAAAAAAC	2186
rs202106844	in-del	-/GTTTTT			intron-variant	BPTF	GRCh38.p7	17:67881852	TTTTGGGGATTTTGG[-/GTTTTT]GTTTTTTTTTTTTTT	2186
rs202116659	snp	C/T			synonymous-codon	BPTF	GRCh38.p7	17:67959642	CCCAGTGACACCAGC[C/T]CCTCCAGCCCCTCCA	2186
rs202135462	in-del	-/G			intron-variant	BPTF	GRCh38.p7	17:67942334	AAAACAAAAAAAAAA[-/G]GACAAACCAACATTA	2186
rs202136205	in-del	-/TA	0.0640965	0.167152	intron-variant	BPTF	GRCh38.p7	17:67973037	TAAAATATATATATT[-/TA]TATATATATATATAT	2186
rs202138842	in-del	-/TATA			intron-variant	BPTF	GRCh38.p7	17:67910819	AAAAAAATATATATA[-/TATA]AATTCCTCCTTTCAG	2186
rs202146930	snp	A/G	0.000729078	0.019079	intron-variant	BPTF	GRCh38.p7	17:67966665	CCTATGGGTAAGTAC[A/G]TGAGTTGAATATGAA	2186
rs202196838	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67967151	CATACTTTTTTTTTC[C/T]TTTTTTAATGAGACG	2186
rs202198196	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67973230	ATACAAAAAATTAGC[A/C]AGGCATGGTGGCAGA	2186
rs202228218	in-del	-/T	0.439918	0.162576	intron-variant	BPTF	GRCh38.p7	17:67910813	TCAAAAAAAAAAATA[-/T]ATATATATAAATTCC	2186
rs202246196	snp	C/T	3.60166e-05	0.00424346	intron-variant	BPTF	GRCh38.p7	17:67875524	CAATTTTAAAGAATA[C/T]CTTTGAAGTTTTGTT	2186
rs367551787	in-del	-/AAA			intron-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67919218	AATAATAATAATAAT[-/AAA]AAAATATAATGCTTG	2186
rs367581152	snp	A/G	0.00993419	0.0697739	intron-variant	BPTF	GRCh38.p7	17:67871536	AATATACAGCTTACT[A/G]TATTTGCTTTATCCT	2186
rs367595898	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67925112	TTGTCATTATTTGAA[A/G]ACAGCTCTGTGGGTA	2186
rs367605541	snp	A/C/G/T	0.000111787	0.00747544	intron-variant	BPTF	GRCh38.p7	17:67959913	TAGTTTTTTGTCTTG[A/C/G/T]AAGTTTAGCTATTAA	2186
rs367655081	in-del	-/GTT			intron-variant	BPTF	GRCh38.p7	17:67829124	TTTTTTGTTGTTGTT[-/GTT]TTTTCTAATTGGTTT	2186
rs367663793	snp	A/C	1.67332e-05	0.00289246	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67929471	CAGGCTCTGGAGGAA[A/C]CACAAGCAATTCACA	2186
rs367671534	snp	A/G	4.94189e-05	0.00497062	synonymous-codon	BPTF	GRCh38.p7	17:67945782	ATCAACTCCATCCCA[A/G]CTGTCTCCTGGACAA	2186
rs367677602	snp	C/G	1.65996e-05	0.00288089	intron-variant	BPTF	GRCh38.p7	17:67944103	AAAATGATATACATA[C/G]AGATTGATGCTTTGA	2186
rs367678846	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67832814	TTTTTTTGAGGCAGA[C/G]TCTCGCTCTGTCACC	2186
rs367697290	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67953339	TCGGCTCCTGCAACC[A/T]CCTCCTCCCAGTTTC	2186
rs367716020	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67942333	AAAAACAAAAAAAAA[A/G]GGACAAACCAACATT	2186
rs367768976	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67961649	CCCAGGTGTTTGAGA[C/T]CAGTCTGGGCAACAT	2186
rs367775856	snp	A/G	4.98633e-05	0.00499291	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67874853	GAGCCAAAAAGGGAG[A/G]CATTGATAATGTTAA	2186
rs367814313	snp	A/T	1.67764e-05	0.00289619	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67826198	GGAGACCCAGGATTC[A/T]GAGGACGACGAGGAG	2186
rs367897161	snp	C/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67971763	GAGCCAAGATCGTTG[C/G]GTTGCAGTGATCTGA	2186
rs367898721	snp	A/G	3.30186e-05	0.00406303	intron-variant	BPTF	GRCh38.p7	17:67966527	GGAAACTTAAATGGA[A/G]TTAGTGTTTTCACTG	2186
rs367923909	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67962146	AGACAAAAGAAAAAA[A/G]GAAAAAAGTTAGTGG	2186
rs367952795	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67943133	GAGGGAATTGAAATC[C/T]GGGTGAGTCATATGG	2186
rs367955857	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67969374	CAAAAATCAGTTGAA[C/T]CTGAGAGGCAGAGGT	2186
rs367966505	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67964555	AACTGCAGTCCTTCA[C/T]GTACCAGTGCCATGA	2186
rs367984764	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67865027	TAACCGGGATGGTCT[C/T]GATCTCCTGACCTTG	2186
rs367992996	snp	C/G	0.000153988	0.00877328	intron-variant	BPTF	GRCh38.p7	17:67904666	ATAAGCATTGTTATT[C/G]TTATTGTTTAATCAA	2186
rs368034271	snp	A/G	6.67858e-05	0.00577827	intron-variant	BPTF	GRCh38.p7	17:67929294	ACGTAATGCTTTCCA[A/G]TAAAGTGATAGTTTT	2186
rs368038500	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67865426	TACCTTTAAGTCTTA[C/T]AGTGGCCTGCAGGCA	2186
rs368068715	snp	A/G	0.00014954	0.00864568	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67826309	GGAAAGCAGCTTCAG[A/G]AGCCATAGTACCTAC	2186
rs368077252	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67827127	CGCGTCTTAACTCAT[C/T]TGATCGCTTTGCCTT	2186
rs368085942	snp	A/G	1.72722e-05	0.00293867	intron-variant	BPTF	GRCh38.p7	17:67909792	TGTGGAGGGCAGCCT[A/G]GGGGTGATAAGAATG	2186
rs368109195	snp	A/G	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67949232	TAGCCAAACATGGTG[A/G]CATACGCCTGTAGTC	2186
rs368113305	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67921020	GAGCCCAGCCTAGAC[A/G]ATGTAGTGAAACCCT	2186
rs368114595	snp	A/T			intron-variant, utr-variant-5-prime	BPTF	GRCh38.p7	17:67889821	CTCAAAAAAAAGAAA[A/T]AAAACCTCCATGATC	2186
rs368116575	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67933859	AAGTCAGGAGTTTGA[C/G]ACCAGCCTGGCCAAC	2186
rs368128741	in-del	-/GAGTATT			intron-variant	BPTF	GRCh38.p7	17:67881164	GATACCCATTATATT[-/GAGTATT]ATCAGTGATCAGAAA	2186
rs368155798	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67974754	AATGCTGTGGGGAGG[A/G]GTGTGGAGTCTCCCA	2186
rs368192443	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67926848	CTTAAGGTGATCCTC[C/T]GGCCTCAGCCTCCTG	2186
rs368214033	snp	A/T	0.00358779	0.0422022	intron-variant	BPTF	GRCh38.p7	17:67884042	ATTTTATGTGTGAAC[A/T]TAGTGATTATCCTCA	2186
rs368230910	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67909488	ATGAAACATAACTTG[C/T]TGGAAATTACTTGTT	2186
rs368233713	snp	A/G	0.000153988	0.00877328	intron-variant	BPTF	GRCh38.p7	17:67866729	TTTTGTTAAGTCTGA[A/G]CTAAACCGTTGGTAT	2186
rs368250011	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67970028	CACCTGAGGTTGGGA[A/G]TTCAAGACCAGCCTG	2186
rs368252808	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67966424	TCTTAGGTAACTATT[-/T]ACTAGAGCAGAAATC	2186
rs368268420	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67960923	TGAATTAAACAGAAA[A/T]CAATTTAGGCATCTT	2186
rs368372407	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67879049	AGTATCAGGAATATT[A/T]TGTCAGTCTTTAGTA	2186
rs368388000	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67832830	TCTCGCTCTGTCACC[C/T]GGGCTGGAGTGGAGT	2186
rs368410600	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67954180	TTTTGGGGTGTTTTT[-/T]GTTGTTATTGTTGTT	2186
rs368414617	snp	A/G	4.02439e-05	0.00448557	intron-variant	BPTF	GRCh38.p7	17:67875756	CCAGGTACAGAGGGC[A/G]GCGTATCAATGCCTC	2186
rs368433751	snp	A/C/T	0.000166749	0.00912953	intron-variant	BPTF	GRCh38.p7	17:67904873	CATGTCCTGCATAAT[A/C/T]GTTTCTGCTTTATAT	2186
rs368465790	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67910809	ATCTCAAAAAAAAAA[-/T]ATATATATATATAAA	2186
rs368469411	snp	A/G	3.32939e-05	0.00407993	missense	BPTF	GRCh38.p7	17:67964394	TGAAGAGGGTGCTCC[A/G]TTCCTTACAGGTGAG	2186
rs368496629	snp	C/T			upstream-variant-2KB	BPTF	GRCh38.p7	17:67825317	GGAGTTTTGCCGCGC[C/T]ACCCGCGCCCGGAGT	2186
rs368507665	snp	C/T	0.000228598	0.0106886	intron-variant	BPTF	GRCh38.p7	17:67826365	CCCAGTTGCTGCAGA[C/T]TCCTTCCCCACCTCC	2186
rs368521311	snp	C/T	0.0193772	0.0965046	intron-variant	BPTF	GRCh38.p7	17:67870926	AGGCGCCCGCCACTA[C/T]GCCCGGCTAATTTTT	2186
rs368532133	snp	C/T	0.000153988	0.00877328	synonymous-codon	BPTF	GRCh38.p7	17:67944353	CACCACCACCACCAC[C/T]GTTTCCACGACAGCA	2186
rs368537118	snp	A/G	1.79348e-05	0.00299451	intron-variant	BPTF	GRCh38.p7	17:67975754	CTCTGAAAATGTTTT[A/G]CATTTTGTGTTTTTA	2186
rs368595283	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67870800	TTTGAGACGGAGTCT[C/T]GCTCTGTCGCCCAGG	2186
rs368597009	snp	A/G	0.0193772	0.0965046	intron-variant	BPTF	GRCh38.p7	17:67918394	ATATTTTGGAATTAG[A/G]TTAACTTTATAAAGT	2186
rs368611376	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67974873	AGGAAAGCTTCATTA[C/T]GTAGGCATGAGTGAT	2186
rs368616840	snp	A/G	3.57309e-05	0.0042266	intron-variant	BPTF	GRCh38.p7	17:67913192	ATCACTTGGAGGTAT[A/G]TACTTTAAAATGTAT	2186
rs368618882	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67857868	CCTTGGCTCACTGCA[A/G]CCTCCATCTCCCAGG	2186
rs368627419	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67934648	TGGGAGGCCGGCGGG[G/T]GGATCACAAGGTCAA	2186
rs368691105	snp	G/T	1.65776e-05	0.00287898	intron-variant	BPTF	GRCh38.p7	17:67904856	GTAAGTAATTAAAAT[G/T]ACATGTCCTGCATAA	2186
rs368702272	snp	A/G	0.000153988	0.00877328	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911348	TGAGTGATCCTAGTC[A/G]TACCACAAACAAACT	2186
rs368737322	snp	A/G	3.29576e-05	0.00405928	missense	BPTF	GRCh38.p7	17:67944157	TTCCACAGGGTGGCA[A/G]TCAAGGTTTGACAGT	2186
rs368793504	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67980065	AAAAACCTACCCAGG[C/G]CGGGTGTGGTGGCTT	2186
rs368796044	snp	A/G/T	0.000174546	0.00934048	intron-variant	BPTF	GRCh38.p7	17:67853918	GTATTGATTTGTAAT[A/G/T]ATGTCACGTCTTTAT	2186
rs368800974	snp	A/G	0.00953873	0.0683987	intron-variant	BPTF	GRCh38.p7	17:67849405	GAATTTCTCTCAAAC[A/G]TGATAATGCCAGTCA	2186
rs368836602	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67967702	CAGGCATTTGTAATC[C/G]CAGCTGCTAAGGAGG	2186
rs368864456	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67923415	AGCTTGACTTTACTC[C/T]ACCTTTGATTTTAAG	2186
rs368867519	snp	A/G			missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67904774	ATTAGTAAAACTCAT[A/G]TTTATAGGTTTGTTC	2186
rs368881161	snp	A/G	0.00438332	0.0466095	intron-variant	BPTF	GRCh38.p7	17:67858743	AGGATGGCTGGGAAC[A/G]AATTAGGAAGTAAGT	2186
rs368883313	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67864766	TGGGCTTTGGAATAT[A/T]TGCATTATACTTACC	2186
rs368886534	snp	C/T	8.29442e-05	0.00643935	intron-variant	BPTF	GRCh38.p7	17:67918667	GAATGTGTATGTGTA[C/T]GTATATACATATAGA	2186
rs368920109	snp	C/T	6.67858e-05	0.00577827	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912133	AATAAACCCAAAATA[C/T]ATTTGAAAGGTGAAT	2186
rs368956376	in-del	-/T	0.439918	0.162576	intron-variant	BPTF	GRCh38.p7	17:67910811	TCTCAAAAAAAAAAA[-/T]ATATATATATAAATT	2186
rs368977614	snp	A/T	1.65567e-05	0.00287716	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67893580	CTTGCACATAAGTTC[A/T]GTCTGACTCCAGCAG	2186
rs368979857	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67864565	AAGAAAAAAGTTAAA[A/C]AAAACAAAACAGACC	2186
rs369067586	in-del	-/ATTTC			intron-variant	BPTF	GRCh38.p7	17:67879132	GGGCTGTTGTTAATT[-/ATTTC]TTTTTTTTTTTTTTT	2186
rs369114066	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67952281	TTTTTTTTTTTTTTT[G/T]GGAAATGGAGTCTTG	2186
rs369120952	snp	C/G	0.000153988	0.00877328	intron-variant	BPTF	GRCh38.p7	17:67940426	CATTCATAATGTTTT[C/G]CTGTTTGGGTAGGTG	2186
rs369238451	snp	A/G	6.66511e-05	0.00577244	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67912615	TGAAAATGTCAATGG[A/G]GAATCTAAAAGAAAA	2186
rs369242186	snp	C/G	4.95323e-05	0.00497631	missense	BPTF	GRCh38.p7	17:67944316	TCTTTACCCCATTGG[C/G]AACAACAGCCACCAC	2186
rs369268023	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67928099	ATATTGGCCAGGCTG[A/G]TCTCGAACTCCTGAC	2186
rs369277559	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67834176	CCCGTATAACCTCCA[A/G]GACCATGTGCATTAA	2186
rs369279593	snp	A/G	6.72823e-05	0.00579971	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912238	ATCCCTGAGAATGAT[A/G]TTAAATCATTGACTG	2186
rs369290675	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67936186	AGCACCAATTCTAAT[A/G]TGAAATATAGCAGGG	2186
rs369302987	snp	C/G	1.66763e-05	0.00288753	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911251	GACTCGATGAGACAA[C/G]AACAGAGCCCAAATG	2186
rs369329934	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67848003	CTGGAGTATTAACTT[C/G]GGCTGGAAATGAACT	2186
rs369338404	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67905911	TGTCGTGGGGTTGGG[A/G]GAGGTTGGGGGATAG	2186
rs369349235	in-del	-/A			intron-variant	BPTF	GRCh38.p7	17:67909291	CCCCTTTTTTTTTTT[-/A]TCCTGCAGTGTTTTA	2186
rs369415074	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67834572	TCTTCATGTATTTTG[A/T]GGCTTTATATTCATG	2186
rs369428261	snp	C/T	3.30841e-05	0.00406706	synonymous-codon	BPTF	GRCh38.p7	17:67948220	ACTAAGCTGTCAGCT[C/T]TGCTCTTCAAGCACA	2186
rs369433491	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67851290	TTTTTTTTTTTTTTT[A/T]AATAACCACCATATA	2186
rs369457219	snp	A/G	0.000148245	0.00860815	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67854519	GTAGGGTTTGTCACA[A/G]ACTTGGGGATTTGCT	2186
rs369460207	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67944769	TTGTTGACCTTCTGC[C/T]GCAAGTCATTGTAAC	2186
rs369465861	snp	A/G			intron-variant, utr-variant-3-prime	BPTF	GRCh38.p7	17:67982052	TTTTTCCAGTGAGCT[A/G]TTATGTTTAGTGTAC	2186
rs369465987	snp	C/G	0.00358779	0.0422022	intron-variant	BPTF	GRCh38.p7	17:67930058	GAGGGGAAGGTTGCA[C/G]TGAGCTGAGATTGTG	2186
rs369468190	in-del	-/TA			intron-variant	BPTF	GRCh38.p7	17:67858670	TAGACATTCAGCAGT[-/TA]TAGCAGGTCACGTTC	2186
rs369482640	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67914632	GTGACCTGGCAGTTG[C/T]GGAGGCCGACCTTTC	2186
rs369489282	snp	A/G	0.0138799	0.0821421	intron-variant	BPTF	GRCh38.p7	17:67964767	GCACTTTGGGAGGCC[A/G]AGGTGGGCGGATCAC	2186
rs369533640	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67935534	TTATTTTGCAAGTCT[A/G]ATCTAGGGAAAAGGG	2186
rs369553954	snp	A/G	1.65061e-05	0.00287277	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911585	TGATCTGTAAGAACA[A/G]AAAACCGCTCATACA	2186
rs369558403	snp	C/T			downstream-variant-500B	BPTF	GRCh38.p7	17:67984630	TTGAAAAACATACTT[C/T]TTTTTTTTTTTTTTT	2186
rs369558728	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67895767	TCTGATAAGAGTGCA[A/G]TTAGTACAGTGGTTG	2186
rs369563983	snp	A/T	3.32602e-05	0.00407786	missense, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67875679	TGGGGTGTCTCTCAG[A/T]AACCCCCGATAGCAG	2186
rs369568346	in-del	-/ACAC/ACACACAC			intron-variant, utr-variant-3-prime	BPTF	GRCh38.p7	17:67981866	CATCAATGTAAATAA[-/ACAC/ACACACAC]ACACACACACACACA	2186
rs369583786	snp	A/T	0.000436088	0.0147599	synonymous-codon	BPTF	GRCh38.p7	17:67940461	TCAGCAAGTGATGAC[A/T]CAAATCATCAGGGGG	2186
rs369586709	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67977768	AGAATCACTTGAATC[C/T]GGGAGGCGGAGCTTG	2186
rs369595757	snp	A/G	0.000214202	0.0103467	missense	BPTF	GRCh38.p7	17:67931989	ACACTAGGAAAGGCA[A/G]TTATTCGAACACCTG	2186
rs369625110	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67951254	AGCCCTGAGAATCAG[C/T]CCCAATCCTGAGGCT	2186
rs369642020	snp	A/G	0.000153988	0.00877328	intron-variant	BPTF	GRCh38.p7	17:67853921	TTGATTTGTAATGAT[A/G]TCACGTCTTTATCTA	2186
rs369645474	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67979540	CAAGAGCAAAACTCC[A/G]TCTCAAAGATAATAA	2186
rs369652266	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67876815	CATCTTAAAAAAGTA[A/T]AAAAAGAGAAAAAGA	2186
rs369701769	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67972245	TTATTTTATTATTTT[A/T]TTTTTTTTGAGAAGG	2186
rs369726104	snp	A/C	0.00688992	0.058288	intron-variant, utr-variant-3-prime	BPTF	GRCh38.p7	17:67982205	AAGCATCATTGTTTT[A/C]AAAAATGAAGGGTGC	2186
rs369797404	snp	G/T	4.94181e-05	0.00497057	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67894091	AGAATTTGCATTGGC[G/T]TTAGCCATTTTGGAG	2186
rs369797684	snp	G/T	4.94214e-05	0.00497074	intron-variant, synonymous-codon	BPTF	GRCh38.p7	17:67946046	AGTCCAGGTTCTCTC[G/T]CAGATCCAGTCACAG	2186
rs369829617	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67976697	CTCAAAAAAAAAAAA[-/T]AAAAAAAAAAAAAAA	2186
rs369835254	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67828305	ACCCAGAGCCGGTAA[A/T]TGAAACACGGAGACT	2186
rs369837099	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67956134	CCATCCTGGCTAACA[C/T]GGTGAAACCCCGTCT	2186
rs369839650	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67847470	AGTGAGCAGAGGTCG[C/T]GCCACTGCACTCCAG	2186
rs369916418	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67835139	TGCTTGAGCCCAGGA[A/G]TTAGAGGCCCTAGTC	2186
rs369927155	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67954729	TGAAGGGAGAGGGAA[C/G]ATCAAAGTGTGTGCC	2186
rs369954466	snp	C/G	0.00438332	0.0466095	intron-variant	BPTF	GRCh38.p7	17:67927125	CAAAGGCAGGAGATA[C/G]TGGTGCAGGATTGGA	2186
rs369980967	snp	A/T			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67887190	AGTATTTCGTATACA[A/T]ATTTACATATTCTTA	2186
rs370005428	snp	C/T	1.65392e-05	0.00287564	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67911067	ATCATCCAAACTAGA[C/T]GGACTTCTTGAAAGG	2186
rs370032796	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	BPTF	GRCh38.p7	17:67982482	AAAAAGCAAAGTCAA[C/T]GACACCATTATCTTG	2186
rs370034055	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67832842	ACCTGGGCTGGAGTG[C/G]AGTGGCGGGATCTCA	2186
rs370063436	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67890587	CTGGCCACGCTGGGT[A/C]CTGCTGCTCGCTCCA	2186
rs370073845	snp	A/G	4.31928e-05	0.00464699	intron-variant	BPTF	GRCh38.p7	17:67940406	TAATGCCAAGGGTGT[A/G]TAAGCATTCATAATG	2186
rs370076082	snp	C/G	0.000343542	0.0131016	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	BPTF	GRCh38.p7	17:67893375	TTTTGGTCAGGTACT[C/G]GTAGTTAACTCTCAA	2186
rs370079727	snp	A/C/G	6.22043e-05	0.00557664	intron-variant	BPTF	GRCh38.p7	17:67948312	TGAAGTGCAGGTAAG[A/C/G]GGGCACATCCTTTTC	2186
rs370105627	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67932489	ATCACTTGAGCCCAG[A/G]AGTTCAAGACCAGCC	2186
rs370107303	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67861252	TTCCCACTGTCCCTC[C/T]GTGATACAAGCCAGT	2186
rs370116546	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67831386	ATTAAACAAAATGAG[A/G]GCCAAAAGGGTTATG	2186
rs370122731	snp	A/C	0.000100185	0.00707691	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67910912	TCTGACAGTGATAAA[A/C]CCTGCAAGGAAGAAC	2186
rs370140857	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67833983	ATCTCCCTTATTTCT[A/C]TTTTCCTTATTCACT	2186
rs370143263	snp	C/T	0.00993419	0.0697739	intron-variant	BPTF	GRCh38.p7	17:67895986	TTTTTTTTTTTGAGA[C/T]GGAGTCTCGCTCTGT	2186
rs370154892	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67964923	AGAATGGCATGAACC[C/T]GGGAGGCAGAGCTTG	2186
rs370159482	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67875032	GAGGGTAAAAAAATT[A/G]CTTGATTAAAAAGAA	2186
rs370166839	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67916634	AGCTGGATGTTTGGG[C/T]GGGCGCCTGTAATCC	2186
rs370170805	snp	A/G			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67888360	TTGGGAGGCCAAGGC[A/G]GGCGGATCACGAGGT	2186
rs370220781	snp	C/T	0.0103295	0.0711199	intron-variant	BPTF	GRCh38.p7	17:67964855	ATACAAAAAATTAGC[C/T]GGGCGTGGTGGCGGG	2186
rs370221851	snp	A/G	0.00358779	0.0422022	intron-variant	BPTF	GRCh38.p7	17:67932418	TAAAAGTTGAAGACT[A/G]GCCAGGCTAGGTGAC	2186
rs370226933	snp	A/G	0.0001035	0.007193	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67913167	TCCTTCTCCTAGACC[A/G]ACCTTTGGCATCACT	2186
rs370229572	snp	A/G	0.0103295	0.0711199	intron-variant	BPTF	GRCh38.p7	17:67879323	ATTTTTGTATTTTTA[A/G]TAGAGACGGGGTTTC	2186
rs370233636	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67836618	TTCATAGAGCCTCAA[A/G]ATACATGAGGACTGA	2186
rs370251416	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67953087	CTGCCTCAGCTTCCC[A/G]AGTAGCTGGGACTAC	2186
rs370266062	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67956318	AGCGAGACTCCATCT[A/C]AAAAAAAAAAAAAAA	2186
rs370273068	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67878685	CTTTATGTGTTCGTG[C/T]GTGTGTGTGTGTGTG	2186
rs370295219	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67938520	ATGATACCAAAGGAA[G/T]CAACACAAATAGTTA	2186
rs370335256	snp	A/G	1.66065e-05	0.00288149	intron-variant	BPTF	GRCh38.p7	17:67918666	TGAATGTGTATGTGT[A/G]TGTATATACATATAG	2186
rs370407205	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67900462	TAGGCCAGGTGTGGT[A/G]GCACATGCCTGTAAT	2186
rs370411790	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67957518	ACCAGCCTAGCCTAC[A/G]TGGTGAAACCCTGTC	2186
rs370449913	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67964751	CATGCCTGTAATCCC[A/C]GCACTTTGGGAGGCC	2186
rs370523864	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67862236	CTGCCTCGGACTCCG[A/G]AAGTGCTGGGATTAC	2186
rs370582295	snp	A/G	0.0023933	0.0345097	intron-variant	BPTF	GRCh38.p7	17:67908792	CACTACACCCATCCA[A/G]ATTTTATCACTCTTG	2186
rs370583774	in-del	-/AC			intron-variant	BPTF	GRCh38.p7	17:67880954	ATGTATATTATATAT[-/AC]ATATACACACACACA	2186
rs370601373	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67850053	TCACTGTAGTCCTGT[A/G]TTTACTTACGTAGAA	2186
rs370629006	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67885539	AGGCTACAGTCAGCC[A/G]AGATTGTGCCACTGC	2186
rs370631037	snp	C/T	5.37861e-05	0.00518557	intron-variant	BPTF	GRCh38.p7	17:67964423	AGACCCCTCTGTGTG[C/T]AGCATTTCAAAATGA	2186
rs370648587	snp	C/T	9.24428e-05	0.006798	synonymous-codon	BPTF	GRCh38.p7	17:67947776	AAAACAGAAAAAGAG[C/T]ATGACTCCAGCTGAA	2186
rs370804353	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67851051	ATTTACACTCACCAG[A/G]CTATGGAGGATTCAT	2186
rs370804480	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67875154	AAGAGATCAGGATAC[C/T]GTCCCCTCTTATAAC	2186
rs370806972	snp	C/T	0.00478085	0.0486577	intron-variant	BPTF	GRCh38.p7	17:67924858	CATCCCTGGTTCAAG[C/T]GGTCCTCAGCCTCCC	2186
rs370807289	snp	A/G	1.65165e-05	0.00287367	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912967	CTGATGAAATTTTCA[A/G]GACCAAAGAAGACTC	2186
rs370812145	snp	A/G	8.59114e-05	0.0065535	intron-variant	BPTF	GRCh38.p7	17:67928618	TATGGAACTATCATT[A/G]AGTAAAAGATTACTT	2186
rs370858180	snp	A/T	0.00438332	0.0466095	intron-variant	BPTF	GRCh38.p7	17:67873913	AGGCTCCTTGGAGAG[A/T]TGGTGGATTGTAGGG	2186
rs370859141	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67952593	TTAGAGCAGTTTTAC[A/G]TGCAGAACGTACAGT	2186
rs370867179	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67879136	TGTTGTTAATTATTT[C/T]TTTTTTTTTTTTTTT	2186
rs370891474	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67863863	CTGTGAGTCATTAAC[C/T]TTCTACTTAGCTAGC	2186
rs370900317	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67964868	GCTGGGCGTGGTGGC[A/G]GGCGCCTGTAGTCCT	2186
rs370917172	snp	C/T	0.0001318	0.00811681	synonymous-codon	BPTF	GRCh38.p7	17:67964260	GTACCATGGGCGCTG[C/T]GTTGGCATCTTGCAA	2186
rs370953212	in-del	-/A			intron-variant	BPTF	GRCh38.p7	17:67956853	ATGTAGCCCCAGCTA[-/A]CTCAGTAGGCTGAGG	2186
rs370961122	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67827117	TACAGGAACGCGCGT[C/T]TTAACTCATTTGATC	2186
rs370983094	snp	A/T	0.0626037	0.165477	intron-variant, utr-variant-3-prime	BPTF	GRCh38.p7	17:67982023	TATATATATATATAT[A/T]TTTAAATATTGGCTT	2186
rs370996802	snp	C/G	0.000153988	0.00877328	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67866612	CGTGAAGAAATCCAC[C/G]GACACATGGACATAA	2186
rs371004763	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67874600	GAGCCCATAATTAGC[A/G]TGTATTATCTAGAGG	2186
rs371004780	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67893912	CACTAACTATTTGGA[A/G]GATTTTTAGGAGTCA	2186
rs371012329	snp	C/T			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67888446	ACAAAAAATACTAGC[C/T]GGGCATGGTGGTGTG	2186
rs371084809	snp	A/G	0.000198007	0.00994807	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67911877	TGAAGTCTTGGAGCC[A/G]TTAAAGTGTGAGTTG	2186
rs371091437	snp	C/T	0.00054893	0.0165579	intron-variant	BPTF	GRCh38.p7	17:67946335	AAACAGGTAAAGTTA[C/T]TAAGTAAAAGCAGCA	2186
rs371111958	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67946580	ACTAAGATGGGAAGA[A/T]TGGAGTTATGAGCTT	2186
rs371141724	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67917151	TTTTTTTTTTTTTTT[G/T]AGATAGAGTCTCACA	2186
rs371208910	snp	C/T	0.00517822	0.0506191	intron-variant	BPTF	GRCh38.p7	17:67947368	GCATAATGTTAAAAA[C/T]ACGGCCTTTGGAGAA	2186
rs371214492	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67909567	CGTAAATTATCGTTA[C/T]ATGGTTCTTTTTAGC	2186
rs371221887	snp	A/G			downstream-variant-500B	BPTF	GRCh38.p7	17:67984843	ATGTTGGTCAGGCTG[A/G]TCTCGAACTCCCGAT	2186
rs371227123	snp	A/G	4.94401e-05	0.00497168	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67911721	CTTTGAAGGAAAACT[A/G]GGATGTGACTCTGAA	2186
rs371238622	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67885998	TTATACATTGCATTA[C/T]TGATACATGAACAGA	2186
rs371241758	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67880119	CATCGTATCTTTTTT[A/G]TATATATAGGGTCTA	2186
rs371257417	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67930931	CTGCACTGCAGTCTA[A/G]GTGACAGAGTGAGAC	2186
rs371307848	snp	C/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67970856	GTGTAGTTTTTGCTA[C/G]TATAAACAACATGCC	2186
rs371337450	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67877608	AAAGCATTTTGGATG[C/T]TAAGATATTTTTGGT	2186
rs371342206	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67964119	AAAACTATTTTATAT[C/T]CCAGGGTTTAGCAAA	2186
rs371346557	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67879071	TCTTTAGTATCAGGA[A/G]TATTTTGGCCTCATA	2186
rs371348387	snp	A/G	0.0178098	0.0926698	upstream-variant-2KB	BPTF	GRCh38.p7	17:67825339	GCCCGGAGTCCAGCC[A/G]CACCGCGCTGTGCCG	2186
rs371356944	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67846041	TATCCTGTTTTGCTA[C/G]TGAAGCAAAATTTTT	2186
rs371357299	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67899001	ACTTATAAATATTGT[C/T]AAGATATAGACACAA	2186
rs371357766	snp	C/G	0.000298201	0.012207	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911513	AGAGTAAAACAAAAG[C/G]AAATGATTTTTTCAT	2186
rs371423442	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67930609	ATGTTCTGAACCTAA[C/T]TATAAAACTGAAAAT	2186
rs371439372	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67870919	GGACTACAGGCGCCC[A/G]CCACTACGCCCGGCT	2186
rs371448601	in-del	-/TTA			intron-variant	BPTF	GRCh38.p7	17:67832646	GTTGTGCAACCATTA[-/TTA]ACACTACCTAATTCC	2186
rs371486729	snp	C/T	0.000285071	0.0119354	intron-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67929509	ATTCTTACAGACTTA[C/T]TTGGTTTGATGTGTT	2186
rs371490474	snp	A/C	1.79981e-05	0.00299979	intron-variant	BPTF	GRCh38.p7	17:67874789	TTATATATAGGAATA[A/C]TTTTTTTGTTTGTTT	2186
rs371490653	snp	A/C	5.50888e-05	0.00524799	intron-variant	BPTF	GRCh38.p7	17:67891820	TATTGTCAGCAATTG[A/C]TTTGTGGCCTATTCA	2186
rs371500398	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67842100	AGCGCCCCTCCCTTA[C/T]GTTATAATTGTACAT	2186
rs371504250	snp	A/T	0.000153988	0.00877327	intron-variant	BPTF	GRCh38.p7	17:67959495	GCCAGATCACACATT[A/T]ACATGACTCTAATGA	2186
rs371569542	snp	A/G	1.6489e-05	0.00287128	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67929341	TTTTTTTAAGGCGTT[A/G]TTCAAGTACAGCAGA	2186
rs371578481	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67864776	AATATTTGCATTATA[A/C]TTACCAGTTGATCAT	2186
rs371591228	snp	A/G	1.7608e-05	0.0029671	intron-variant	BPTF	GRCh38.p7	17:67853896	AAATTTGTAGAAATG[A/G]TGTAATGTATTGATT	2186
rs371607236	snp	A/G	1.66632e-05	0.0028864	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912623	TCAATGGAGAATCTA[A/G]AAGAAAAACCGTCAT	2186
rs371614689	snp	A/G	1.6703e-05	0.00288985	missense	BPTF	GRCh38.p7	17:67944366	ACTGTTTCCACGACA[A/G]CAGCAGGTAGAGCTG	2186
rs371630071	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67966011	AGTGAGCTATGATCA[C/T]GCCACTCGACACCAG	2186
rs371641728	snp	A/C			intron-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67918893	AGCTAAAATCACAGG[A/C]CAGGCGTGGGCGCTC	2186
rs371644151	snp	C/T	3.29685e-05	0.00405995	synonymous-codon	BPTF	GRCh38.p7	17:67940545	GCAGAAAAGCTTAAC[C/T]TCAGCAACGTCCACT	2186
rs371645761	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67962147	GACAAAAGAAAAAAA[G/T]AAAAAAGTTAGTGGT	2186
rs371647134	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67955381	CCCTGCAAAAAAGGG[G/T]CACAGCAAACTCTAT	2186
rs371674717	in-del	-/AATT			intron-variant	BPTF	GRCh38.p7	17:67876107	CTGTAGATACTAACA[-/AATT]AATTTTATGTTTGCA	2186
rs371697268	snp	C/T	9.37954e-05	0.00684755	intron-variant	BPTF	GRCh38.p7	17:67947832	GACGCAGGGTCTTGT[C/T]GTCTGTCCGTCTCTT	2186
rs371723265	snp	A/T	0.000153988	0.00877328	intron-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67918849	GACAGGTAAGGGGGA[A/T]GGGAGTTATTTTCTA	2186
rs371725227	snp	A/G	0.000153988	0.00877328	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67874955	AAGAATTTGAAGACC[A/G]GTCCCTTGAAAAAGA	2186
rs371725263	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67948592	TTTTCATGTCTATGA[C/T]ATAGTCTAGCCAAAA	2186
rs371731638	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67942972	CTGCCTGGAGGGGGC[A/C]CTATTCCCATTGTAT	2186
rs371743743	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67884485	CAATGGCGCAATCAC[A/G]GCTCACTGCAGCCTC	2186
rs371747743	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67855988	GGCTGCTTTCATCCA[C/T]GAGGTATTTTTGGTG	2186
rs371765804	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67894336	ATTATTAGTTCTTTC[-/T]TTTTTTTTTTGAGAC	2186
rs371766058	snp	G/T	0.133093	0.220981	intron-variant	BPTF	GRCh38.p7	17:67840490	TGCTGCTGCTGCTCC[G/T]CCGCCTCCTCCTTCC	2186
rs371816958	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67858494	TAGGAGGCGGAGGTT[A/G]CAATGAGCCGAGATG	2186
rs371817782	snp	C/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67826473	AGAGGGGAAATGCGA[C/G]GGCACATCAAGTGGC	2186
rs371823434	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67949556	CTCTAGCCTGGACAA[C/T]AGAGTGAGACTCCAT	2186
rs371824893	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67953559	CACCATGCCCGGCCC[A/G]TCAAATTGTTCTATA	2186
rs371842346	snp	A/C	2.00995e-05	0.00317007	intron-variant	BPTF	GRCh38.p7	17:67909536	ACATATTAAAGTGCT[A/C]ATACTCTGGAAATAA	2186
rs371845051	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67832825	CAGAGTCTCGCTCTG[C/T]CACCTGGGCTGGAGT	2186
rs371847873	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67853118	TCCAGCCTAGGCGAC[A/G]GCTGTAGGTGATTAA	2186
rs371873845	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67902194	TCATGGACACCAAGA[A/G]CACAACTGAGCACCC	2186
rs371883660	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67943186	GGTGACCACAGTGGC[A/G]GTTTTATAGATGTTT	2186
rs371885163	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67933962	GGCAAGAGAATTGCT[C/T]GAACTCAGGAGGTGG	2186
rs371888651	snp	A/C			missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912314	TGGAAGATTTTAATG[A/C]AAGAAACAGCTCCGA	2186
rs371891881	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67827457	ATAGTCACAATTTAC[C/T]AAATTGTGAAATTAA	2186
rs371924672	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67922503	ATTGACATTAGTCAG[A/G]TGAGCGGTGGAGGCT	2186
rs371934607	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67833238	CTTCATTGTATGGCT[A/C]TACAGCCTTTTTTTT	2186
rs371943059	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67865501	CTTAGAGACTCAGAG[A/G]GGCTGTGTCTTGTCC	2186
rs371952607	snp	A/G	1.67066e-05	0.00289016	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912170	AAGAAATTTCTGAGA[A/G]TAGAGTAGTAAGTGG	2186
rs371954848	snp	C/T	1.82961e-05	0.00302452	synonymous-codon	BPTF	GRCh38.p7	17:67945569	AACCCAGCCCCAGTC[C/T]CCAGCTCAGCCTGAA	2186
rs371990788	snp	A/G	1.72033e-05	0.0029328	intron-variant	BPTF	GRCh38.p7	17:67886098	TTCATGTGATTTCCA[A/G]TTTAAAAATCAGATA	2186
rs372002315	in-del	-/GT			intron-variant	BPTF	GRCh38.p7	17:67837257	GAATGTGCTAGAGAT[-/GT]ACCTTTAGTCACTTA	2186
rs372033433	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67970310	AGACTGAGGCAGGAC[A/G]ATCACTTCAGCTGGG	2186
rs372038942	snp	A/G/T	4.94241e-05	0.00497092	synonymous-codon, missense	BPTF	GRCh38.p7	17:67944167	TGGCAATCAAGGTTT[A/G/T]ACAGTAGTAATTCAA	2186
rs372078899	snp	A/G	3.3151e-05	0.00407117	intron-variant	BPTF	GRCh38.p7	17:67918676	TGTGTATGTATATAC[A/G]TATAGATATATATGG	2186
rs372103353	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67959425	AACTAAAACTCTCAC[A/G]TTAGGCTGAACTGTG	2186
rs372113045	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67923146	CTGCAACCTCTGCCT[C/T]CCAGGCTCGAGTGAT	2186
rs372232080	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67926526	AGACGGGGTTTCACT[A/G]TGTTAGCCAGGATGG	2186
rs372268649	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67832403	TTTTATGTTTTTCTA[A/G]ATAGTAAGTTATATT	2186
rs372320737	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67846513	GCACCTGAAATTTTT[C/G]TTCAGGTCTCATACT	2186
rs372337155	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67832831	CTCGCTCTGTCACCT[A/G]GGCTGGAGTGGAGTG	2186
rs372372873	snp	G/T	5.04214e-05	0.00502077	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67826195	CGAGGAGACCCAGGA[G/T]TCTGAGGACGACGAG	2186
rs372397198	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67846897	GTAGAGACAGGGTTT[C/T]GCCATGTTGGCCAGG	2186
rs372398987	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67834394	ATTTTGTATTCTGCT[C/T]TTGTTGAGTGGAGTA	2186
rs372440339	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67858687	AGCAGGTCACGTTCA[C/T]GCAGTCTCAAGTGCC	2186
rs372446429	snp	A/T	3.59751e-05	0.00424102	intron-variant	BPTF	GRCh38.p7	17:67959884	AATCTAAGTGAGTAG[A/T]TCTTTTTGAGCTCTA	2186
rs372482515	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67852205	TATACAAGACTATGA[A/G]TAGTCATTAGTGGCA	2186
rs372545332	snp	A/C	4.94401e-05	0.00497168	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67911652	TGCTTTACATTCATC[A/C]GTGCCTAAAAGTACC	2186
rs372551122	snp	C/T	3.30077e-05	0.00406236	missense	BPTF	GRCh38.p7	17:67940511	TCTCCGCCCCTAACA[C/T]GGTTTCCTCAACACC	2186
rs372561178	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67892279	ATACACTTTCTTACT[A/G]CATGAACAGTTTTAT	2186
rs372573333	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67923813	GTGTTGTCCATTTGT[C/T]GATTTCTAATGACCA	2186
rs372575812	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67834091	CATCCATCCATCACC[C/T]TCTCCAGCCTGCCTT	2186
rs372578116	snp	C/T	1.848e-05	0.00303968	intron-variant	BPTF	GRCh38.p7	17:67875069	CATTAGTGTTATTTA[C/T]GAAATCTCCAGTTTT	2186
rs372590463	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67914153	GCGAGTTACTGAGCC[A/G]TTTTCATTTCCCCTT	2186
rs372625079	snp	C/T	1.65381e-05	0.00287555	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911354	ATCCTAGTCATACCA[C/T]AAACAAACTTTATCC	2186
rs372687302	snp	C/T	0.00438332	0.0466095	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67888370	AAGGCGGGCGGATCA[C/T]GAGGTCAGGAGTTCG	2186
rs372693974	in-del	-/G	0.0566477	0.158477	intron-variant	BPTF	GRCh38.p7	17:67931040	ACTTTGGGAAGCCAA[-/G]GGGGGCGGATCACAA	2186
rs372696064	snp	A/G	1.67961e-05	0.00289789	missense	BPTF	GRCh38.p7	17:67945429	GGTGAACAAAGGCAG[A/G]GTAAACTGTCACCCC	2186
rs372746103	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67965052	TTCCTTATGAAAAAC[A/G]AAAAGGGGACTGGGC	2186
rs372755648	snp	A/G	0.0107246	0.0724382	utr-variant-3-prime, downstream-variant-500B	BPTF	GRCh38.p7	17:67983240	ATGAAAGGCAGAAGA[A/G]TCTAATTGTGCCTGG	2186
rs372829722	snp	A/C/G/T	0.000214138	0.0103454	missense, synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67854607	GGAGGTGCCAGAGGA[A/C/G/T]GAGTGGCAGTGTGAA	2186
rs372833652	snp	A/G	3.30147e-05	0.00406279	intron-variant	BPTF	GRCh38.p7	17:67932026	TACAGCCAGGTATTT[A/G]TCCATCCAGCATTAT	2186
rs372837861	snp	C/T	6.58935e-05	0.00573955	missense	BPTF	GRCh38.p7	17:67945843	CCGATTCCAATTCAA[C/T]CACATACATCTCTTC	2186
rs372870037	snp	C/T	0.000153988	0.00877328	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67854022	TGAATTTCCCAAGTC[C/T]TCTGAGGATTTAATG	2186
rs372886058	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67864570	AAAAGTTAAACAAAA[A/C]AAAACAGACCAAAAA	2186
rs372887341	snp	A/C/G	6.60288e-05	0.00574549	intron-variant	BPTF	GRCh38.p7	17:67944135	CACTGTTTACATGTT[A/C/G]TGTTTTTTCCACAGG	2186
rs372907851	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67879766	AGCAAATAGGGGAGG[C/T]GGGGGTGGCAGATGA	2186
rs372936943	snp	C/T	1.66499e-05	0.00288525	synonymous-codon, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67875683	GTGTCTCTCAGAAAC[C/T]CCCGATAGCAGCAAC	2186
rs372946073	snp	A/G	0.000166661	0.00912704	synonymous-codon, utr-variant-3-prime	BPTF	GRCh38.p7	17:67982267	GTCTCATAACAACAA[A/G]CTGCAGTCTACAGCT	2186
rs372953315	in-del	-/TTTTGAAGATGT			intron-variant	BPTF	GRCh38.p7	17:67898673	AGTCTTTTTTTTTTT[-/TTTTGAAGATGT]ATTGCAAACCAAATT	2186
rs372995703	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67976698	CTCAAAAAAAAAAAA[A/T]AAAAAAAAAAAAAAA	2186
rs373035730	snp	A/G	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67956163	CTCTACTAAAAATAC[A/G]AAAAAATTAGCCGGG	2186
rs373067728	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67952695	TAATGAGCCAATAGT[G/T]ATTATTATTATTATT	2186
rs373081863	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67845168	GTTCCATTATTGATA[A/T]AGATCACTTGGTAAA	2186
rs373088510	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67830510	GCTGCATGCGAGGTA[C/T]GCAGTGCAGTGGGCA	2186
rs373110669	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67872583	TGGTGGTATGCGCCT[A/G]TAGTCTCAGCTACTT	2186
rs373114855	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67873331	GGTGTGGTGGCAGGC[A/G]CCTGTAATCCCAGCT	2186
rs373124058	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67916493	TACTCAGGAGACTGA[A/G]GCAGGAGAATCACTT	2186
rs373144211	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67961833	GCAAAAATTAGCCAG[A/C]TGTGGTGGCACACAC	2186
rs373165270	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67896079	GCCATTCTCCTGCCT[C/T]AGCCTCCCGAGTAAC	2186
rs373191978	in-del	-/TCCT			intron-variant	BPTF	GRCh38.p7	17:67931542	TTTGGTTTCTGATCT[-/TCCT]GTTATATTCTGTGGG	2186
rs373208222	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67894286	TTTACTTTTGGCCTC[A/G]TTTTCTTCCTATATA	2186
rs373208409	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67844404	AGGCGCCCGCCACCA[C/T]GCCTGGCTAATTTTT	2186
rs373221403	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67867659	ATGGCCTTGACAGTT[A/G]GGAGGAGTAGTGGTT	2186
rs373222562	snp	A/C	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67890001	TCTGTTTAAAACAAA[A/C]ATCTGTGGAATGTGA	2186
rs373226797	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67944969	CGTCCTGCCCTAAGC[A/G]TGTCCAAATGGAGCA	2186
rs373244486	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67972592	AAAGTTTCATAGATT[C/T]TTTGGCATATGGTAG	2186
rs373244547	snp	C/G			intron-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67929880	GAACACTTTGGGAGG[C/G]CAAGGCGGGTGGATC	2186
rs373292551	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67906965	GGCAGGGGAGGATCA[A/G]TTGAGCCCAGGAGTT	2186
rs373341614	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67951169	TTACATCATTGGCTG[G/T]TGGTGGTCAGCTTAA	2186
rs373360978	snp	A/G	0.00517822	0.0506191	intron-variant	BPTF	GRCh38.p7	17:67930031	TGAGGTGGGAGGATG[A/G]CTTGAGCCTGGGAGG	2186
rs373370380	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67863353	GCAGTGGCACGATCT[C/T]GGCTCACTGCAACCT	2186
rs373400357	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67951853	ATGAGGCCAGGAGTT[C/T]GAGACCAGCCTGGCT	2186
rs373402896	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67980664	AAATTGCCTGGAGGT[C/T]CTGGGGACTGTAGGC	2186
rs373459164	in-del	-/TCTT			intron-variant	BPTF	GRCh38.p7	17:67856137	TTGGTCTTCTGACTT[-/TCTT]ATCATTTCTCTCCAG	2186
rs373529800	snp	A/G	1.65408e-05	0.00287578	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67854714	ATGAACCTATTGGAT[A/G]TGATAGAAGTCGGAG	2186
rs373557198	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67872810	TTCTTTAAAATATAG[G/T]AATTAAGGGCTGGGC	2186
rs373565663	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67828467	TATGCTGACTTAAAT[G/T]ACAATTTGTAGCTAG	2186
rs373568866	in-del	AA/C			intron-variant	BPTF	GRCh38.p7	17:67901314	ATTGTTAAAAAAAAA[AA/C]AACCCAGAACCCTAA	2186
rs373573165	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67850493	TCTGCCTCAGCCTCC[C/T]AAGTAGCTGGGAGTA	2186
rs373593090	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67975038	ATCTAGGGAATTCCA[A/G]CCACCAGTCATTAAC	2186
rs373601884	in-del	-/TT			intron-variant	BPTF	GRCh38.p7	17:67953749	CCAGCTAATTTTTTT[-/TT]GTGTATTATTCGGAG	2186
rs373625057	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67967552	TTGGAAATGGCGGGG[G/T]GGCTCACGCTGGAAT	2186
rs373636454	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67893349	ACATAAATAATGCAG[A/T]CTTTTTATTTTTTTG	2186
rs373668743	snp	C/T	1.64727e-05	0.00286986	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67854396	ACCCATATGGACCAG[C/T]AGAGAACAAGATCAA	2186
rs373672145	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67915570	CTCTTTCTGTACCTC[C/T]ACACCCCTTCCCTCC	2186
rs373712501	snp	A/G			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67897247	TCGGGAGGCTGAGGC[A/G]TGAGAATCGCTTGAA	2186
rs373767294	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67861507	TTTTAGTAGAGACAG[A/G]GTTTCACCATGTTGG	2186
rs373776384	in-del	-/A			intron-variant	BPTF	GRCh38.p7	17:67964797	AAGGTCAGGAGATCA[-/A]GACCATCCTGGCTAA	2186
rs373778856	in-del	-/AC			intron-variant	BPTF	GRCh38.p7	17:67925991	GTAACCTAACATATT[-/AC]TTTTTTTTTTTTTTT	2186
rs373785754	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67895836	TTAAAAATGCAATTC[A/G]ACTCCTTCCTAGTAC	2186
rs373786127	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67852443	TATATATATACCTTA[C/T]CACTATCCCCTTGCC	2186
rs373826616	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67832809	TTTTTTTTTTTTGAG[A/G]CAGAGTCTCGCTCTG	2186
rs373856552	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67932560	AAAAATTAGCTGGGC[A/G]TGGTGCCTCATGCAC	2186
rs373874484	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67857680	CCATGTTACTCAGGC[C/T]GATCTCGAACTTGTG	2186
rs373891210	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67900834	GGGCAACATAGCAAG[A/G]CTCTGTCTCTACAAA	2186
rs373897951	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67958679	GAGGTTGGAGTGCGC[A/T]GAGATTGTGCCACTG	2186
rs373933480	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67834208	TGTTTTAGTTTCCAA[A/G]TATTTGGGAATTTTT	2186
rs373955177	snp	A/G	1.65026e-05	0.00287246	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67903885	GATGCAGCAAGCGAC[A/G]TGGGTAAAATACACA	2186
rs373959573	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67950045	GGCAACAGAATGAGA[C/T]TGTCTCAAAAAAAAA	2186
rs374007542	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67926549	CAGGATGGTCTCGAT[C/T]TCCTGACCTCGTGAT	2186
rs374031452	snp	A/G	1.66156e-05	0.00288228	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67893613	GAGTTCAAATGGAAC[A/G]GTTCTGTCCATGGGT	2186
rs374037905	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67961933	GAGCCGAGATCATGC[C/T]ACTGTACTCCAGCCT	2186
rs374040359	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67956641	TTAAAGAAGGAAAAA[A/T]AAAATTAATTCAGTT	2186
rs374085799	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67906518	AGCCGATTATTTCAC[A/G]AGGGTGCCAGGTGAC	2186
rs374093486	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67880848	AACATTCTATGCATG[A/G]TTTATGTCCTTTAAA	2186
rs374167713	snp	A/C	1.6577e-05	0.00287893	intron-variant, missense	BPTF	GRCh38.p7	17:67946237	AGCAACTCAGGGATC[A/C]GCAGCAAAAGAAGAA	2186
rs374172446	snp	C/T	9.92572e-05	0.00704406	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67912882	GACAGACTCCCTGAC[C/T]ACCACGGGAGGCACA	2186
rs374176300	snp	C/G	1.76421e-05	0.00296998	synonymous-codon	BPTF	GRCh38.p7	17:67945545	GCCTTCAGCTCAGCC[C/G]CAGCCCCAAACCCAG	2186
rs374190306	snp	A/C/G			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67898046	CCAATCTCCAATACT[A/C/G]GGAGATTACTAATAC	2186
rs374191997	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67856978	GAGACACCCCTCCTT[G/T]TTATCATTGCGTTTT	2186
rs374198932	snp	A/G	8.38371e-05	0.00647391	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67826199	GAGACCCAGGATTCT[A/G]AGGACGACGAGGAGG	2186
rs374203346	snp	A/G	0.000103754	0.00720183	intron-variant	BPTF	GRCh38.p7	17:67893735	ACATAGGTAAAGGAA[A/G]CTAAGGTTAATTTAT	2186
rs374215070	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67870262	TTTTTCTTTCTTTCC[-/T]TTTTTTTTTTTTTTC	2186
rs374215371	snp	C/T	0.000445857	0.0149241	intron-variant	BPTF	GRCh38.p7	17:67903954	TTAAAATAGTGTTAG[C/T]CATTTCTGAGACTTT	2186
rs374235007	snp	A/G/T	6.71175e-05	0.0057926	utr-variant-3-prime	BPTF	GRCh38.p7	17:67982297	TTCTTAAAGTTCAGC[A/G/T]TGTTAACCTAACATA	2186
rs374246806	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67876015	ATATTTTATCACCAG[A/C]CCATAGTGGCAGATA	2186
rs374250870	snp	C/T	0.00716266	0.059414	intron-variant	BPTF	GRCh38.p7	17:67956832	AGCCGAGTGTGGTGG[C/T]GGGCGCATGTAGCCC	2186
rs374259078	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67883691	AGCAACCTCCGCCCC[C/G]CTGGGTTCAAGCAGT	2186
rs374290475	snp	A/G	6.59e-05	0.00573983	synonymous-codon	BPTF	GRCh38.p7	17:67964350	CATGACAGTGCTCAC[A/G]CCACTAACAGAGAAG	2186
rs374294135	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67961074	AAATGATTTCTGAAA[C/G]AGGAGTTTCCTTACT	2186
rs374303635	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67899660	CTCAGCCTCCTGAAT[A/G]GCTGGTATTATAGGC	2186
rs374318795	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67845780	TGTCTCAAAAAATAT[A/G]TATATTTTATTTTAT	2186
rs374336120	in-del	-/TTGAGAGAAGCAT			intron-variant	BPTF	GRCh38.p7	17:67914944	ATTTGAGAGAAGCAT[-/TTGAGAGAAGCAT]AATCCTTTCTGTCTA	2186
rs374348067	snp	A/G	1.70685e-05	0.00292129	intron-variant	BPTF	GRCh38.p7	17:67866442	TCTAACATATAAAGT[A/G]TTTCCCCCCATTTTT	2186
rs374349661	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67875442	TTGCTTTAAAATGGC[C/T]GTTCAATGGAAGCAG	2186
rs374357593	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67902259	TGAAGTCCTTCAGAC[A/G]GTGCTCCATTCCTGG	2186
rs374363773	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67879532	TTTCATTCACTTCTT[C/T]AGTAGATAATGGCTA	2186
rs374379938	snp	C/T	9.95471e-05	0.00705433	intron-variant	BPTF	GRCh38.p7	17:67947699	TGATTATAAAATATG[C/T]GCTTTTGGATTTATT	2186
rs374388586	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67832184	TGAGCTGCCGTACCC[A/G]GCCTCTAATTTTTTT	2186
rs374388764	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67837242	AGACAGTGCTGTCCT[A/G]AATGTGCTAGAGATG	2186
rs374392132	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67923621	AGTAGCTGGGATTAC[A/G]GGGGTGTGCCACCAT	2186
rs374415449	snp	A/G	0.000153988	0.00877328	intron-variant	BPTF	GRCh38.p7	17:67918684	TATATACATATAGAT[A/G]TATATGGATTTCTTT	2186
rs374415724	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67959342	TCTAGTTGTTCTTAC[C/T]TAGTCTTCATTTTGT	2186
rs374420324	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67839041	CTGCAAAAATGAATC[A/C]TATGTACACATCTGA	2186
rs374442857	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67978306	ATATATATATATATA[-/T]TATTTTTTTTGAGAC	2186
rs374445207	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67850749	ACAGAATTCTATCCA[A/G]TGAATAAGCCACAAT	2186
rs374454268	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67875295	TATTCTTTAATATTA[G/T]ACCAGAGTATACACT	2186
rs374465606	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67980005	CCACTACACTCTAGC[C/G]TGGGCAACAAGAGTG	2186
rs374472902	snp	A/G	3.49443e-05	0.00417982	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67913177	AGACCGACCTTTGGC[A/G]TCACTTGGAGGTATG	2186
rs374475839	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67905919	GGTTGGGGGAGGTTG[A/G]GGGATAGCATTAGGA	2186
rs374481889	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67852741	GTGACTACAGGATAA[A/G]TTCCAGGAGGTGGAA	2186
rs374492803	in-del	-/GAGTA			intron-variant	BPTF	GRCh38.p7	17:67877026	TTCTCTTCTTGAGTA[-/GAGTA]AAAAACAAAACAATG	2186
rs374501073	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67910541	GTGGTGGCTCATGCC[C/T]GTAATCTCAGCACTT	2186
rs374530575	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67942323	CAAAAAAAAGAAAAA[A/C]AAAAAAAAAAGGACA	2186
rs374536515	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67833202	TATCTTAACATGTAT[C/G]AGTACTATATTTGAA	2186
rs374542465	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67890200	TAGAAATACATCAAA[C/T]TTGCTTAAAAAGGGA	2186
rs374544588	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67910681	GGCACATGCCTATAA[A/T]CCCAGCTACTTGGGA	2186
rs374590899	in-del	-/A			intron-variant	BPTF	GRCh38.p7	17:67956662	AATTCAGTTCTACTT[-/A]AAAAAAAAAAAAAAA	2186
rs374597377	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67869162	AAAATAGACAAATCC[C/G]TTTTTGCTCTCCTGT	2186
rs374598293	in-del	-/TTC	0.00953873	0.0683987	intron-variant	BPTF	GRCh38.p7	17:67921659	AAATTAACTTGGGAG[-/TTC]TTCTTGGAGAATAAC	2186
rs374632412	snp	A/G	3.29761e-05	0.00406041	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911819	TTGTTCAGAATAGCA[A/G]TGAAAGCATTTCTGA	2186
rs374632678	snp	A/G	0.00191995	0.0309239	intron-variant	BPTF	GRCh38.p7	17:67964447	AAAATGAAATCAGCC[A/G]GCATAATTTTGGAAG	2186
rs374633820	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67966041	GCCTGAATGACAGAG[C/T]GAGACCCTGTCTCAA	2186
rs374794915	snp	C/G	0.000153988	0.00877328	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67922973	GGAATTGTGGGAGAT[C/G]AGGGCATTTGCTGAG	2186
rs374796324	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67953701	CTGCCTCAGCCTCCC[C/G]AGTAGCTGGGATTAC	2186
rs374809788	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67930988	AAAGATTAGCTGGGC[C/T]GGATGCGGTGGCTCA	2186
rs374814465	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67933442	GGCATCCTGGAGCAC[A/G]CCTGTAGTCCCAGCT	2186
rs374820823	snp	A/G			intron-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67919278	TGGTGGCTCTCACCT[A/G]TAATCCTAGCACTTT	2186
rs374824193	snp	A/G	0.000167263	0.0091435	synonymous-codon	BPTF	GRCh38.p7	17:67945434	ACAAAGGCAGAGTAA[A/G]CTGTCACCCCAGATG	2186
rs374828111	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67971265	TGTATTTTTGGTAGA[A/G]TCAGGGTTTCACCAT	2186
rs374828863	snp	G/T			intron-variant, utr-variant-5-prime	BPTF	GRCh38.p7	17:67889600	ATCACTGGAGGTCAG[G/T]GGTTCAAGACCAGCC	2186
rs374861723	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67976727	AAAATAAGAATAAAA[A/G]AAGAATTTCCTGAGC	2186
rs374898106	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67838483	CATGTGTATGTACAT[A/C]CTTTTTTTTTTGAGC	2186
rs374898176	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67882133	AGCTACCGTGCTGGC[C/T]GGACTTCTTGCTTTT	2186
rs374899488	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67847907	AAAGATTTCAATGCA[G/T]CACAGGTTATTTCTT	2186
rs374904683	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67902403	GTCACCCCGCCTTAC[G/T]CCTGTAGCCTGAGAC	2186
rs374905004	in-del	A/GGT			intron-variant	BPTF	GRCh38.p7	17:67913357	CAAAATTGGCCAACT[A/GGT]ATGTACTAAAGTTTT	2186
rs374906214	snp	A/G	9.17305e-05	0.00677177	synonymous-codon, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67875740	GCTCCCCCAGGATGT[A/G]CCAGGTACAGAGGGC	2186
rs374907101	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67835212	TGAGAACCCATCTCT[A/T]AAAAAAAAAATTTAA	2186
rs374907644	snp	C/T	6.60186e-05	0.00574499	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911591	GTAAGAACAAAAAAC[C/T]GCTCATACAGGAGGA	2186
rs374945475	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67926266	TGCCTACCAGGGCCT[A/C]CCAAAGTGCTGAGAT	2186
rs374956238	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67968969	CTGGGTAACAAAAGC[A/G]AAACTCCATCTCAAA	2186
rs374958211	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67826466	CCCAAACAGAGGGGA[A/G]ATGCGACGGCACATC	2186
rs374963794	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67953118	AGGCGCAGGCTGCAA[C/T]GCCTGGCTAGTTTTT	2186
rs375029743	snp	C/T	0.00358779	0.0422022	intron-variant	BPTF	GRCh38.p7	17:67856127	ACTTCCTATTTTGGT[C/T]TTCTGACTTTCTTAT	2186
rs375044019	snp	A/G	4.96578e-05	0.00498261	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67909694	TGAGGTAAAAGGTTC[A/G]GATGCTGCAAAAGGA	2186
rs375068422	snp	G/T	8.67434e-05	0.00658515	intron-variant	BPTF	GRCh38.p7	17:67892084	AATGTGAGATAATTT[G/T]AATTACCACACCTTA	2186
rs375070328	snp	C/T	0.000153988	0.00877328	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67912384	TAACTACCGAGATAG[C/T]CTTGAGACCCTGCCA	2186
rs375071850	snp	A/G	4.94173e-05	0.00497053	missense	BPTF	GRCh38.p7	17:67944243	GTGACTGTACTCCCA[A/G]GCCCAGGCCAGCAGC	2186
rs375106085	snp	A/G			intron-variant, utr-variant-5-prime	BPTF	GRCh38.p7	17:67889624	ACCAGCCTGACCAAC[A/G]TGGTGAAACCCCGTC	2186
rs375107621	snp	G/T	0.000153988	0.00877328	missense	BPTF	GRCh38.p7	17:67945757	GTCCATCACAGACTC[G/T]AATACGTCCATCAAC	2186
rs375116157	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67966361	GCTCCATTCCCAACA[C/T]AAAGTCTTCTGACCA	2186
rs375121975	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67948637	AGCTTCATGAGAAAG[A/G]TACAGAGACAGTGAA	2186
rs375167785	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67905850	AAATGAGGTTTTTCA[C/G]TGAGAACATTTGGAC	2186
rs375214270	snp	A/G	0.000153988	0.00877328	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67866613	GTGAAGAAATCCACC[A/G]ACACATGGACATAAC	2186
rs375219937	snp	C/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67960795	ATAAAATTGTGGTCC[C/G]TTTAATGATGTTCAA	2186
rs375239645	snp	A/G	1.66674e-05	0.00288676	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67913121	CTTATTTTAATTACA[A/G]TGCAAAACCTGCTTT	2186
rs375245234	snp	A/T	3.38106e-05	0.00411147	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67874817	TTTTACACATTATAG[A/T]AGAAATTTTGGAATC	2186
rs375264910	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67971946	ACACTGAGTATTATC[A/C]CTCTTTTGAGGGGTA	2186
rs375275463	snp	A/G	9.36373e-05	0.00684178	intron-variant	BPTF	GRCh38.p7	17:67947820	AAAGGTAGGGGAGAC[A/G]CAGGGTCTTGTTGTC	2186
rs375333412	snp	A/G	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67918052	GATCTGCCCACCTCG[A/G]CCTCCCAAAGTGCTG	2186
rs375357953	in-del	-/TTTTTTTTT			intron-variant	BPTF	GRCh38.p7	17:67908827	AGTTGTCACTGACAA[-/TTTTTTTTT]TTTTTTTTTTTTTTG	2186
rs375367797	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67970507	TCTCTAAAACGTATT[A/G]TTGGGAAAAGAAGTG	2186
rs375374576	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67953898	TAATTTCATTTGGAG[G/T]GAATTCAGATTAGAC	2186
rs375396029	in-del	-/A			intron-variant	BPTF	GRCh38.p7	17:67950527	CATCAAAACCCCAAG[-/A]AAAATAATTATTACA	2186
rs375421418	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67942844	TATATAATGGTAAGC[C/T]AAAGAAGCAAGTAGC	2186
rs375425842	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67891565	GTAAGTTTGTAGCAG[C/G]TCTTCCTGTTTTCAA	2186
rs375435089	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67949864	GTTCAAGACCAGCCT[A/G]GCTAACGTGGTGAAA	2186
rs375440648	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67876168	CAAACCGTAGTATTA[C/T]GGTAGAAAATCATTA	2186
rs375441210	snp	A/G	3.32038e-05	0.00407441	intron-variant	BPTF	GRCh38.p7	17:67931898	AATTCATTGTTCTTT[A/G]TGTCATTTATAGGTA	2186
rs375441477	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67923161	CCCAGGCTCGAGTGA[C/T]CCTCCCACCTCAGCC	2186
rs375448679	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67873177	TAAGTGTTTCTTATG[G/T]CCCGGTGCAGTGGCT	2186
rs375452036	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67828944	GCTCCTGTAACAGAG[A/T]TTTGCACATAGCAGG	2186
rs375475492	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67971172	CAACCTCAGCCTCCC[A/G]GGTTCAAGCAATTCT	2186
rs375516255	in-del	-/G			intron-variant	BPTF	GRCh38.p7	17:67955452	AATTTTGGCAGGGGG[-/G]AATCAGGTTTTCCTG	2186
rs375542979	snp	C/T	1.67136e-05	0.00289076	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67912012	AGTTAATAAATGTAG[C/T]GATCAAATAAAGCTA	2186
rs375556593	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67924499	CTTATTAGATGCCAG[A/G]TGCCTAACAGGCTAG	2186
rs375577789	snp	C/G	0.000164845	0.00907719	missense	BPTF	GRCh38.p7	17:67940539	ACCTGGGCAGAAAAG[C/G]TTAACTTCAGCAACG	2186
rs375641091	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67879048	TAGTATCAGGAATAT[A/T]TTGTCAGTCTTTAGT	2186
rs375641696	in-del	-/TAAGAA			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67897995	AGTAAATTTAAAGAA[-/TAAGAA]ACCATGGCTGAATTG	2186
rs375673836	in-del	-/TCAATAAAT	0.00438332	0.0466095	intron-variant	BPTF	GRCh38.p7	17:67923044	TTTATCACTTCAGAA[-/TCAATAAAT]TCAATAAATTACTTT	2186
rs375693144	snp	C/T	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67883899	CCACCGCGCCCGGCT[C/T]GTTTTGTTTTTTATA	2186
rs375696457	snp	A/G	1.65509e-05	0.00287666	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911402	ATGATGTCTCCATTC[A/G]GAGCCCAGAAACAAA	2186
rs375711468	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67951014	GTTTCACCATTTTTT[-/T]GTCAGGCTGGTCTCG	2186
rs375793981	snp	A/C	3.29473e-05	0.00405864	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67854634	TGAAGTCTGTGTAGC[A/C]CACAAGGTGCCTGGT	2186
rs375794302	snp	C/T			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67887547	TCTTTATAATACTTC[C/T]ATAACTTTGTTTTCA	2186
rs375804596	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67916164	CTGCTCTGTCCAGGT[C/G]AGAGGATTCATAGTG	2186
rs375811658	snp	A/G	6.58989e-05	0.00573978	missense	BPTF	GRCh38.p7	17:67945711	CAGCCTCAAAGTAAT[A/G]TCCAAGGACAGTCTC	2186
rs375814587	snp	A/G/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67897373	AAAAAAAAAAAAAAG[A/G/T]AAAGAAAGAGACATA	2186
rs375829008	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67870863	CAAGCTCCGCCTCCC[A/G]GGTTCACGCCATTCT	2186
rs375879274	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67879840	GTGAGAACTCACTCA[C/T]CCCCAACACCCAACC	2186
rs375882496	snp	A/C	0.00874735	0.0655527	intron-variant	BPTF	GRCh38.p7	17:67924416	CACCTCGCACAACCA[A/C]ATGTTTTATTTTTAA	2186
rs375884837	snp	G/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67871061	CAGGCGTGAGCCACC[G/T]CGCCCGGCCGAAAAT	2186
rs375901066	in-del	-/C	0.00358779	0.0422022	intron-variant	BPTF	GRCh38.p7	17:67937312	AATACAAAAAATTAG[-/C]TGGGCATCATGGTTG	2186
rs375917957	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67874635	GGTACACCAAATTGA[G/T]TGAATTCTGTAAACA	2186
rs375928543	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67924057	AGGCTGGAGTGCAGT[A/G]GCACAATCTCGGCTC	2186
rs375931264	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67840854	AGGCATGAGCCACCA[G/T]GCCCAGCCAATTTCT	2186
rs375972303	snp	G/T	1.6752e-05	0.00289408	intron-variant	BPTF	GRCh38.p7	17:67919983	TGAGTATTTCAGTTG[G/T]TTATTAATACTATTG	2186
rs375972460	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67877903	CTCTCAAAAGTGCTG[A/G]GATTACAGGCATGAG	2186
rs375972695	snp	A/C	3.34627e-05	0.00409026	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67929470	TCAGGCTCTGGAGGA[A/C]CCACAAGCAATTCAC	2186
rs375973781	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67927964	TCTCAGCTTACTGCA[A/G]CCTCTGCCGCCTGGG	2186
rs375974109	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67964541	TGAAGTGCCTAACAA[A/G]CTGCAGTCCTTCACG	2186
rs375975293	snp	A/G	3.33139e-05	0.00408116	missense, utr-variant-5-prime, nc-transcript-variant	BPTF	GRCh38.p7	17:67893404	AAGGAGAAATTTCAC[A/G]GTTGAGCACCAAAAA	2186
rs375983597	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67832828	AGTCTCGCTCTGTCA[C/T]CTGGGCTGGAGTGGA	2186
rs375997445	snp	A/G	0.00279162	0.0372561	intron-variant	BPTF	GRCh38.p7	17:67952635	TCCTCCCCCACCCAC[A/G]CACAATTTCCCCTAT	2186
rs375997569	snp	A/G	9.39717e-05	0.00685398	intron-variant	BPTF	GRCh38.p7	17:67947833	ACGCAGGGTCTTGTT[A/G]TCTGTCCGTCTCTTC	2186
rs376007577	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67925657	ACATTGAGGATACAA[A/G]TGAGTAGATATATCT	2186
rs376009178	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67946411	TGGTTGTGTTAGGTT[C/T]CCTAAATGAGACAAA	2186
rs376012134	snp	C/G			utr-variant-3-prime	BPTF	GRCh38.p7	17:67983854	CTCAGTTTCTTAAAA[C/G]AAAGATGTTGCTACA	2186
rs376034250	snp	A/G	1.65184e-05	0.00287384	intron-variant	BPTF	GRCh38.p7	17:67894197	CCTTGTAAATGATGA[A/G]TATTGGACTCCCTTT	2186
rs376036493	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67846393	GGTAGTCCCTAGATG[A/T]ATCTCTAGACCAGGG	2186
rs376040376	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67891249	CAGAAATTTGCTCCT[A/G]TGGAGTTTAGTGTGT	2186
rs376041236	in-del	-/TTAA			intron-variant	BPTF	GRCh38.p7	17:67917618	TGTTTTTGGTTTAAT[-/TTAA]TTAATTAATTAATTA	2186
rs376042155	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67900395	CAGGCGTTAGCCACC[A/G]CGTTCAGCCAAATGT	2186
rs376048162	snp	A/G	1.65318e-05	0.002875	intron-variant	BPTF	GRCh38.p7	17:67920151	ACCAAAAGGTAAGAA[A/G]TAGAATTCTATTCTT	2186
rs376065153	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67936089	TTCTTGGAAATGGGT[A/G]GGAAATAATTTTCTT	2186
rs376171611	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67865191	TCAAAAACTTTTGGA[A/T]CTTGGAGCATTTTGG	2186
rs376184826	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67916786	AAAAAAAAAAAAAAA[A/G]AAAGCATTGCCTTTT	2186
rs376288660	snp	A/G	0.000102759	0.00716722	synonymous-codon	BPTF	GRCh38.p7	17:67948273	CCTGAAGAAGAGAGC[A/G]CTCCTGGACAAGGAT	2186
rs376295354	snp	C/T	3.33751e-05	0.0040849	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67913122	TTATTTTAATTACAA[C/T]GCAAAACCTGCTTTG	2186
rs376307135	snp	C/T	0.00180744	0.0300075	intron-variant	BPTF	GRCh38.p7	17:67948045	CCTTTCAAAATGAAA[C/T]GCCCAGCATTACATA	2186
rs376322340	in-del	-/A			intron-variant	BPTF	GRCh38.p7	17:67942333	AAAAACAAAAAAAAA[-/A]GGACAAACCAACATT	2186
rs376335246	snp	A/G	0.000153988	0.00877328	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911234	AAGAAGGGTGTCAGA[A/G]TGACTCGATGAGACA	2186
rs376393454	snp	A/C	3.49791e-05	0.0041819	intron-variant	BPTF	GRCh38.p7	17:67966673	TAAGTACATGAGTTG[A/C]ATATGAAGTTTTTCA	2186
rs376418219	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67910438	GAACTACATTGTCTT[A/T]TGTAACAAGTCATTT	2186
rs376422599	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67936151	AAAGATAGATAAAAT[A/C]TTTCCCATTTTACTA	2186
rs376436493	snp	C/G	1.65754e-05	0.00287879	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911318	GTTCAGAAAGTGATT[C/G]CTCAGTTCTTAGAAT	2186
rs376444979	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67956234	TGAGGCAGGAGAATG[A/G]CGTGAACCCGGGAGG	2186
rs376453698	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67863826	TTCTATGGGTTTGTT[C/T]AGAAACGAAAGTTGA	2186
rs376456802	snp	C/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67873487	AAGAAAAAGAAAAAC[C/G]GTGTTTCTTCTTATT	2186
rs376467866	snp	C/T	0.000153988	0.00877328	intron-variant	BPTF	GRCh38.p7	17:67959895	GTAGATCTTTTTGAG[C/T]TCTAGTTTTTTGTCT	2186
rs376480270	in-del	-/C			intron-variant	BPTF	GRCh38.p7	17:67899533	TGCTGAGTTTTTTTT[-/C]TTTTTTTTTTTTTTT	2186
rs376492193	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67942510	AGAGCAGAAAGAATT[C/T]TCATGCACAGCTGGT	2186
rs376509218	in-del	-/C			intron-variant	BPTF	GRCh38.p7	17:67879154	TTTTTTTTTTTTTTT[-/C]TTTTTGAGATGGAGT	2186
rs376556898	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67867472	GTGAAATATTTGTTA[C/T]AACTAATGGACCAGT	2186
rs376565339	snp	A/G			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67888374	CGGGCGGATCACGAG[A/G]TCAGGAGTTCGAGAC	2186
rs376568579	snp	A/G			intron-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67929940	GGGCAACATGGCAAA[A/G]CCCCATCTCTACAAA	2186
rs376585771	snp	C/T	8.41659e-05	0.00648659	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912227	TAAATAAAATAATCC[C/T]TGAGAATGATATTAA	2186
rs376598029	snp	A/G	0.00438332	0.0466095	intron-variant	BPTF	GRCh38.p7	17:67922626	GCCTACCCTGCTTTT[A/G]TAAATGAAATTTGAT	2186
rs376600062	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67862004	TTTTTTGATACAAGT[A/C]TCACTCTGTCGCCCA	2186
rs376602912	snp	C/G	3.3227e-05	0.00407583	missense, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67875672	AGCCCTGTGGGGTGT[C/G]TCTCAGAAACCCCCG	2186
rs376606835	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67902794	TTTCGGCATCACTAC[A/C]CCAAGTTAACAAAAG	2186
rs376649045	snp	G/T			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67887061	GTGATGGCTACTGCT[G/T]AATTGTATATCAAAA	2186
rs376661089	snp	A/G	1.74882e-05	0.00295699	intron-variant	BPTF	GRCh38.p7	17:67826362	CAGCCCAGTTGCTGC[A/G]GACTCCTTCCCCACC	2186
rs376681748	snp	G/T	1.92684e-05	0.00310384	intron-variant	BPTF	GRCh38.p7	17:67940423	AAGCATTCATAATGT[G/T]TTGCTGTTTGGGTAG	2186
rs376694768	snp	A/G	3.48335e-05	0.00417319	intron-variant	BPTF	GRCh38.p7	17:67909801	CAGCCTGGGGGTGAT[A/G]AGAATGCACTGGATC	2186
rs376694913	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67955549	GTAGCTTCAGAGGCC[C/G]GGCACGGTGGCTCAT	2186
rs376695680	snp	C/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67922686	TATTGTCTTTGGCTG[C/G]TTTCATGATACAAAG	2186
rs376696681	snp	A/G			synonymous-codon	BPTF	GRCh38.p7	17:67944311	ATTCCTCTTTACCCC[A/G]TTGGCAACAACAGCC	2186
rs376697190	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67864552	AAAAAAAAAGGAAAA[A/G]AAAAAAGTTAAACAA	2186
rs376714209	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67866000	TGGCACATGTCTGTA[A/G]GTCCTAACTACTTGG	2186
rs376753217	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67858930	AAAACCTTGACATCT[G/T]TAAGGCTCATTACAC	2186
rs376801664	in-del	-/TTCTTCTCTGATAA			intron-variant	BPTF	GRCh38.p7	17:67879049	GTATCAGGAATATTT[-/TTCTTCTCTGATAA]TGTCAGTCTTTAGTA	2186
rs376816304	snp	C/G	6.59685e-05	0.00574281	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911833	AATGAAAGCATTTCT[C/G]AACAGTTCAGAACTC	2186
rs376867695	snp	G/T	0.0051927	0.0506891	intron-variant	BPTF	GRCh38.p7	17:67886375	TTTTTTTTCTTTTTT[G/T]TGTGTGTGTGTGTGT	2186
rs376872787	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67931154	CCTGTGATCCCAGCT[A/G]CTTGGGAGGCTGAGG	2186
rs376881244	snp	A/G	0.000437904	0.0147905	intron-variant	BPTF	GRCh38.p7	17:67947865	CTTTATCGTGCACAC[A/G]CACAGAGTTCTGAGT	2186
rs376927939	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67878684	TCTTTATGTGTTCGT[G/T]TGTGTGTGTGTGTGT	2186
rs376968442	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67882955	GTCAACTGAGATCAC[A/G]CCACGCCACTGCACT	2186
rs376969849	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67839652	CTTTATTGCTGAGTA[G/T]CAGTCCCTTATATGA	2186
rs376976745	in-del	-/C	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67907075	CTGTATTCCCAGTTA[-/C]TCAGGAGGCTGATGA	2186
rs377006267	snp	A/C/G	6.61292e-05	0.00574986	intron-variant	BPTF	GRCh38.p7	17:67894015	TGAAATAATTTCTCT[A/C/G]ATTTCTTCTGAAATA	2186
rs377016350	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67937889	GGAGGCCAAGGCGGG[C/T]GGATCACCTGTGGTC	2186
rs377036020	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67953039	GATCTCGGCTCACTG[C/T]AAGCTCCGTCTCCCC	2186
rs377063280	snp	A/G	9.90164e-05	0.00703551	intron-variant	BPTF	GRCh38.p7	17:67903931	CAGGTAATTTTTACA[A/G]CAACCCTTTAAAATA	2186
rs377120148	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67869827	TCTCTACTAAAAATA[A/C]AAAAAAAAAAAAAAA	2186
rs377144909	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67940022	CCCAGAATATTCCAG[A/T]TTCTTTATATTTTGT	2186
rs377147094	snp	C/G	0.000340379	0.0130412	intron-variant	BPTF	GRCh38.p7	17:67866450	ATAAAGTATTTCCCC[C/G]CATTTTTAAACAGAG	2186
rs377147209	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67892281	ACACTTTCTTACTAC[A/G]TGAACAGTTTTATTC	2186
rs377148940	snp	G/T	0.00517822	0.0506191	intron-variant	BPTF	GRCh38.p7	17:67835968	CCATGCCTGGCCCAG[G/T]CCTGGTAAAATTAAG	2186
rs377156769	snp	C/G	1.6795e-05	0.0028978	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67909754	GATTACTGAGAAGAA[C/G]GACCAAGGTAAGGAG	2186
rs377165734	snp	A/T	9.26741e-05	0.0068065	synonymous-codon	BPTF	GRCh38.p7	17:67947749	GAAGCATAATGCTGT[A/T]ATAGAACATTTAAAA	2186
rs377168031	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67930116	GCCAGACCTTGTCTC[A/C]AAAAAAAAAAAAAAA	2186
rs377180088	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67868796	TCTCACATATTCTAC[A/G]TCAATATTCCTGTGA	2186
rs377201949	snp	C/T	0.000153988	0.00877328	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67854245	AATACTACCTTTGGA[C/T]CTGCTGATCTGAAAG	2186
rs377205071	snp	C/T	0.000103589	0.00719611	intron-variant	BPTF	GRCh38.p7	17:67910846	CTTTCAGAGTAAAAA[C/T]TACATTTATATAAAT	2186
rs377266897	in-del	-/AAT			intron-variant	BPTF	GRCh38.p7	17:67976695	GTCTCAAAAAAAAAA[-/AAT]AAAAAAAAAAAAAAA	2186
rs377268645	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67903240	AATCAGAAATACTGG[C/T]TGATAAAATAAATGT	2186
rs377269543	snp	A/G	1.64732e-05	0.0028699	intron-variant, synonymous-codon	BPTF	GRCh38.p7	17:67945992	ACAAATACAGCAGCC[A/G]CAGCCCCAAGTCATT	2186
rs377275656	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67968613	GAAACCCCGTGTTAG[C/T]CCGTCTCTACTAAAA	2186
rs377277090	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67832839	GTCACCTGGGCTGGA[C/G]TGGAGTGGCGGGATC	2186
rs377322742	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67974543	TCTTCAGATGCCGGT[C/T]GCCAGCCCCAGGTGG	2186
rs377347333	in-del	-/G			intron-variant	BPTF	GRCh38.p7	17:67981148	TGTGCTACAGAGTGA[-/G]ACCTTGTTTCAAAAC	2186
rs377442367	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67974981	TCCCAACCCTCCAAT[A/C]CTGACTAGGTCTTTC	2186
rs377508429	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67861144	AATGGAATTACTGTC[C/G]CACCAGCTGCTCAAG	2186
rs377533941	snp	A/G	0.000153988	0.00877328	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67866544	CAGAATTAATTGACT[A/G]TCTAGACAAAGATTA	2186
rs377534417	snp	C/T	0.000153988	0.00877328	intron-variant	BPTF	GRCh38.p7	17:67893996	TAATTTAAGGTCAAC[C/T]TAGTGAAATAATTTC	2186
rs377534845	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67961176	CAGATCACAGAAATT[C/G]ATTTCACACACAACT	2186
rs377590970	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67949227	AAAATTAGCCAAACA[C/T]GGTGGCATACGCCTG	2186
rs377610827	snp	A/G	1.65323e-05	0.00287505	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67912897	CACCACGGGAGGCAC[A/G]CTGGTTACATCTATG	2186
rs377683246	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67830689	ATAGTAAAGTGTGGG[A/C]AGTCTCAAGTAACTC	2186
rs377684552	in-del	-/A			intron-variant	BPTF	GRCh38.p7	17:67916113	TTGGGACATCCCTGC[-/A]ACTAGTTAACATTTC	2186
rs377684654	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67850732	TTACTCAAAATTGAT[C/G]TACAGAATTCTATCC	2186
rs377685980	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67859843	ATCAGTATCAGTCTA[C/T]GAAACAGCATTCAGG	2186
rs377686539	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67880997	TATATATATTACATA[C/T]ATATATTTCAGGCTT	2186
rs377708005	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67930526	TTCTTTGTTACTAGT[A/G]TGGAAAAGGCTTAAA	2186
rs377711345	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67957018	CCCGGCACGGTGGCT[C/T]ACGCCTGTAATCCTA	2186
rs377739813	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67977971	GTGGTTCTCTTGCCT[C/T]AGCCTCCCTAGTAGC	2186
rs377740180	snp	A/G	0.0023933	0.0345097	intron-variant	BPTF	GRCh38.p7	17:67968658	CCGGGTGTGGTGGCG[A/G]GCACCTGTAGTCCCA	2186
rs377741615	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67952844	ATCCCGTGTGCCACC[C/T]TCTTGTTCCTCCTCT	2186
rs386798622	multinucleotide-polymorphism	GT/TC			intron-variant	BPTF	GRCh38.p7	17:67844693	GGGGTGAACCACTGC[GT/TC]CCAGTCTGTTGCCTT	2186
rs386798623	in-del	AGTTT/TA			intron-variant	BPTF	GRCh38.p7	17:67845168	GTTCCATTATTGATA[AGTTT/TA]GATCACTTGGTAAAG	2186
rs386798624	multinucleotide-polymorphism	AG/CA			intron-variant	BPTF	GRCh38.p7	17:67891441	TTTAAACAGAATTTC[AG/CA]TGGAAATCTTTCAAA	2186
rs386798625	multinucleotide-polymorphism	AAG/TAA			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67897526	ACCAAGATGGTGGAA[AAG/TAA]AAGTCCCCAACTCAT	2186
rs386798626	multinucleotide-polymorphism	CG/TA			intron-variant	BPTF	GRCh38.p7	17:67916951	AGTTACACAAAGATA[CG/TA]TAGTGAATTCCATTT	2186
rs386798628	multinucleotide-polymorphism	ATC/TTG			intron-variant	BPTF	GRCh38.p7	17:67975266	AGTGGACACTTATCA[ATC/TTG]CAGTCATGAATGGTA	2186
rs386798629	multinucleotide-polymorphism	AA/CC			intron-variant	BPTF	GRCh38.p7	17:67975488	CATGTCGGTGTGTTT[AA/CC]TTGATTTCAAACCAT	2186
rs397737670	in-del	-/A			intron-variant	BPTF	GRCh38.p7	17:67852003	TTGATAATGAGTGTA[-/A]ATGCTCAGTGGCATA	2186
rs397857458	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67881499	CCATAATCAAGGTTT[G/T]TTTTTTTTTTTTTTT	2186
rs398031411	in-del	-/G	0	0	intron-variant	BPTF	GRCh38.p7	17:67826589	GAAAAAAAGGGGGTT[-/G]GGGGGGGGGAGAGAG	2186
rs398031412	in-del	-/GT	0	0	intron-variant	BPTF	GRCh38.p7	17:67880979	ATGTAATATATATAC[-/GT]GTGTGTGTGTGTGTG	2186
rs398079124	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67851930	GGTCCTTTTTTTTTT[-/T]TAATGCAGGAAAATT	2186
rs398079125	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67863947	CTCTTAATTATATTT[-/T]TAGCAAACCTTTTCT	2186
rs398119966	in-del	-/A			intron-variant	BPTF	GRCh38.p7	17:67835222	CTCTTAAAAAAAAAA[-/A]TTTAAGTAAAATGAA	2186
rs398119967	in-del	-/A			intron-variant	BPTF	GRCh38.p7	17:67852004	TGATAATGAGTGTAA[-/A]TGCTCAGTGGCATAT	2186
rs398119968	in-del	-/CT			intron-variant	BPTF	GRCh38.p7	17:67852463	TCCCCTTGCCCTCCT[-/CT]TTTTATTTTTAGTTT	2186
rs398119969	in-del	-/GGAT			intron-variant	BPTF	GRCh38.p7	17:67874029	GATGGATGGATGGAT[-/GGAT]ATGTGTCAAAAGGAC	2186
rs527239164	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67830473	TATCAGTGTCAATAT[C/G]TTTTCAGTATAATTT	2186
rs527263582	snp	A/T	0.00597247	0.0543191	intron-variant	BPTF	GRCh38.p7	17:67975680	CAGGACTGCTTGCAC[A/T]GTAAACATATATACT	2186
rs527270786	snp	C/T	0.00358779	0.0422022	intron-variant	BPTF	GRCh38.p7	17:67870970	GAGACGGGGTTTCAC[C/T]GTTTTTTAGCCAGGA	2186
rs527275032	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67968739	CTTGCAGTGAGCCAA[G/T]ATTGTGCCACTGCGC	2186
rs527285169	snp	C/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67829392	TGTGCAGAACGTGCA[C/G]GTTTGTTGCATAGGT	2186
rs527289673	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67926849	TTAAGGTGATCCTCC[A/G]GCCTCAGCCTCCTGA	2186
rs527324318	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67871614	AAGTTTATTTTTAGA[A/G]GAATTTTTTCTGAGT	2186
rs527338892	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67964723	TAGTTGTTCTTGGCC[A/G]GGCATGGTGGCTCAT	2186
rs527366649	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67836285	ACACGCTTGGGAAAC[A/G]GCATGGCCATGTGAT	2186
rs527403277	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67964090	AATCTTGAAAGTATT[A/G]AAACCATAATACTAA	2186
rs527427995	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67927862	AAAATATATATATGG[C/T]CTTCATCAAGAAATT	2186
rs527434875	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67828135	TGGGGTTTCACCATG[C/T]TGGCCAGGCTGGTCT	2186
rs527457816	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67981250	TTTCTATTGTTTTCC[A/G]GATTTAAGGCAGAAT	2186
rs527465590	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67891487	TATACAGAAATCCAT[A/G]TTGAATATATAAGGC	2186
rs527513585	in-del	-/AA			intron-variant	BPTF	GRCh38.p7	17:67951385	GAAGATCAAATATAT[-/AA]ATTTCACAGTATCAC	2186
rs527540836	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67974769	GGTGTGGAGTCTCCC[A/G]TGCCCTCTCTGGGCA	2186
rs527554547	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67935037	CATATTTGAACACCT[A/C]CTCTAGGCAGTTGAA	2186
rs527578347	snp	C/T	0.0023933	0.0345097	intron-variant	BPTF	GRCh38.p7	17:67849275	ACCAGATGATTTTTG[C/T]TGCACCTCCATTTCA	2186
rs527581489	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67899797	GCTTCCCAAAGTGCT[A/G]GGATTACAAGCATGA	2186
rs527590553	snp	A/T	0.00279162	0.0372561	intron-variant, utr-variant-3-prime	BPTF	GRCh38.p7	17:67982056	TCCAGTGAGCTATTA[A/T]GTTTAGTGTACAGTG	2186
rs527611931	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67948658	AGACAGTGAAGTAAC[A/G]TTGAAAGAATGAAAA	2186
rs527615814	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67942054	CCTGTAATCCCAGCA[C/T]TTTGGGGGGCCAAGG	2186
rs527616947	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67934490	CACCACTGCACTGCA[G/T]CCTGGGCAACAAGAG	2186
rs527643370	snp	C/T	6.63713e-05	0.00576032	intron-variant	BPTF	GRCh38.p7	17:67904860	GTAATTAAAATTACA[C/T]GTCCTGCATAATCGT	2186
rs527656773	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67862706	AAAACTGGGTAGTTT[A/C]AAACAGTAGAAATTG	2186
rs527659865	in-del	-/A	0.00358779	0.0422022	intron-variant	BPTF	GRCh38.p7	17:67861544	GATATTGAACTCCTG[-/A]ACCTCAGGTGATCAG	2186
rs527708690	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67919612	TCCCAGGGGCCAGAA[A/G]GGAAGGTTCAGATTA	2186
rs527716073	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67856260	CCAGTTTTTCCTTTC[C/T]GCTACCATATTTTTA	2186
rs527722181	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67961772	TGAGGTCAGGAGTTC[A/G]AGATCAGCCTGGCCA	2186
rs527738515	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67949446	TGGGCGTGGTGGCAG[A/G]CACCTGTAATCCCAG	2186
rs527780222	snp	C/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67905423	AAAAAAAAAAAAATT[C/G]AGGCCAGCCACAGTG	2186
rs527783660	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67917172	GAGTCTCACACTGCC[G/T]CCCGAGGTGGAGTGC	2186
rs527796880	snp	A/G			intron-variant, utr-variant-5-prime	BPTF	GRCh38.p7	17:67888691	AATTTAACTGCCTAT[A/G]ACACTCATAAACATA	2186
rs527799339	snp	C/T	0.00557542	0.0525036	intron-variant	BPTF	GRCh38.p7	17:67956044	GGGTCTCGGGCCAGG[C/T]GCAGTGGCTCACGCT	2186
rs527839788	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67895832	AAAGTTAAAAATGCA[A/G]TTCGACTCCTTCCTA	2186
rs527847093	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67973838	ACTCCTTTCCCTACT[A/G]ACTTGAAGGGACACC	2186
rs527852789	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67871070	GCCACCGCGCCCGGC[C/T]GAAAATGCTTCATTT	2186
rs527890072	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67838844	AAATATTTTCACTTA[C/T]GCCATGAAATCAGAT	2186
rs527890547	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67933447	CCTGGAGCACGCCTG[A/T]AGTCCCAGCTACTTG	2186
rs527893769	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67924833	TAGATCACAGCTCAC[C/T]GAGCCTCGACATCCC	2186
rs527931307	snp	A/G	0.00159617	0.0282053	utr-variant-3-prime	BPTF	GRCh38.p7	17:67982589	AGAAAAAAAGATACT[A/G]TGGGGTCAAGTGTAA	2186
rs527932610	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67972953	TTTCACAGTTCTTCA[C/T]ATTTACACATTTTTT	2186
rs527946023	snp	C/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67882739	GGGCTGGGCGTGGTG[C/G]CTGACGCCTGTAATC	2186
rs527964260	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67835473	CTTGGGTAGCCCCAG[C/T]ACTCTGGCTGAGTGA	2186
rs527966169	snp	A/G	0.0023933	0.0345097	intron-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67919009	AACCCCGTCTCTACT[A/G]AAAATACAAAAAATT	2186
rs527973522	in-del	-/GAACTGGCGC			intron-variant	BPTF	GRCh38.p7	17:67864858	CACCCAGGCTAGAGT[-/GAACTGGCGC]GAACTCGGCTCACTC	2186
rs527981281	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67967601	CAAGGTGGATGGATC[A/G]CCTGAGGTCAGGAGT	2186
rs528006432	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67875860	CATGCTGCTTGCTTA[C/T]AGTGCCATCCCCATT	2186
rs528011948	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67883189	GGCGTGATGATGGGC[A/G]CCTGTAGTCTCAGCT	2186
rs528017842	snp	G/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67826500	TGGCAAAAAACTAGA[G/T]TTACAAGAGGAAAGA	2186
rs528023638	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67925633	GTTTTTACCAACTTC[A/G]GTATATAAACATTGA	2186
rs528024126	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67835151	GGAGTTAGAGGCCCT[A/C]GTCAGCTATGGACCA	2186
rs528038241	snp	C/T	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67956008	ATTCTCTGGGTGTTA[C/T]GATACACGCCTGTAA	2186
rs528045378	snp	C/T	0.00318978	0.0398085	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67896412	GGGGCACAAGGGTTG[C/T]AAAAATTACCTGTTG	2186
rs528065035	snp	A/G	0.000399281	0.0141238	synonymous-codon	BPTF	GRCh38.p7	17:67947800	AGCTGAAAGAGAAGA[A/G]AATCAAAGGTAGGGG	2186
rs528097202	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67840593	GTTTCCTTCTTTCAC[C/T]CATGCTGGAGTGCAG	2186
rs528168518	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67932121	GAAATATAATTTTAA[G/T]TAGTACTTCAAAGCA	2186
rs528189790	snp	A/T	0.00795532	0.062565	intron-variant	BPTF	GRCh38.p7	17:67846287	TTGGGCCCAGCAGTT[A/T]TAGAGCAGCCTGGGC	2186
rs528194964	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67854837	GATTGATGTAGCAGA[A/G]CTATGCTGTTGATGT	2186
rs528205552	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67939648	TTTGGGAGGCCAAGG[C/T]GGGTGGATCACGAGG	2186
rs528205729	snp	C/T	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67979498	GCAGTGCACCAAGAC[C/T]GCGCCACTGCACTCC	2186
rs528229545	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67910299	CCTCTTTTGGCTATA[C/T]GAATAATGCTGCTAT	2186
rs528240288	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67971161	TCGGCTCACTGCAAC[C/G]TCAGCCTCCCGGGTT	2186
rs528266124	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67860741	TATTTCATTTTTTTG[A/C]AGAGACAGAGTCTCA	2186
rs528290188	snp	C/T	0.0115144	0.0749975	intron-variant	BPTF	GRCh38.p7	17:67953446	TGTTTTTTGAAGAGA[C/T]AGGGTTTTGCCATGT	2186
rs528327370	snp	G/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67861238	TCAGTTTCTCTCCAT[G/T]CCCACTGTCCCTCCG	2186
rs528331492	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67853875	GGGGGTATATGTTCA[A/G]ATAGGAAATTTGTAG	2186
rs528337621	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67966333	ATACTGATTTTGTGA[C/T]TTCTAAGCTTGTGCT	2186
rs528342480	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	BPTF	GRCh38.p7	17:67825171	CGAGCCGCGAAAGGG[C/G]AGACGCGGGGAGGAG	2186
rs528365396	snp	A/T	0.00517822	0.0506191	intron-variant	BPTF	GRCh38.p7	17:67910807	TCCATCTCAAAAAAA[A/T]AAATATATATATATA	2186
rs528371790	snp	A/C/G			intron-variant	BPTF	GRCh38.p7	17:67844990	TCAAGTAATCCATCC[A/C/G]CCTCAGCCTCCCAAA	2186
rs528379821	in-del	-/A			intron-variant	BPTF	GRCh38.p7	17:67942257	AGAAGCAGAGGTTGC[-/A]GCGAGCCAAGATATA	2186
rs528402596	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67954201	TATTGTTGTTGTCGT[C/T]GTTTTTTTGTAGAGA	2186
rs528421160	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67848737	TTTTGTGTTACAGAA[G/T]ACAAAGGAGCAGAAA	2186
rs528451627	snp	C/T	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67971580	GGAGGCTGAGGCAGG[C/T]GGATCATGAGTTCAA	2186
rs528458343	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67863222	CTTCTGGCAGTCCTT[A/T]GCATTTCTTGGTTTA	2186
rs528489114	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	BPTF	GRCh38.p7	17:67824384	TCATCCGGCCTTGGC[C/T]TCTCAAAGGACTGGG	2186
rs528496927	snp	A/G	0.0023933	0.0345097	intron-variant	BPTF	GRCh38.p7	17:67931063	CAAGGTCAAGAGATC[A/G]AAACCATCCTGGTCA	2186
rs528514584	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67977947	ACAAGCCCCACCTCC[C/T]GGATTCAAGTGGTTC	2186
rs528532716	snp	G/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67866994	CAATGGCAGGTATTT[G/T]TGTATCTAACTATAT	2186
rs528550976	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67916923	GTAGAGTGAAAATGT[C/T]AACAAAGTATTCAGT	2186
rs528553753	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67965473	GAGGCCAAGGCAGGA[A/G]GATCACTTGAGTCAA	2186
rs528563778	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67923719	TCCTGACCTTGGGTA[A/T]TCCACCTGCCTCAGC	2186
rs528579805	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67839328	TTTTTTTTCCTAAGT[C/T]TTTTTTTAAAAAAAA	2186
rs528601033	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67965976	TGAGGTGAGAGGATC[A/G]CTTGAGCACAGGAGG	2186
rs528614142	snp	G/T	0.000399281	0.0141238	downstream-variant-500B	BPTF	GRCh38.p7	17:67984450	GTTAGCCTTGCCAAA[G/T]TGTACAAAAAGGATA	2186
rs528644198	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67931516	AATTTTTAAAAAACT[A/G]TGAAAGAACATTTGG	2186
rs528645055	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67901934	AAATATTGTTTGTTA[C/T]AGCTATGGCTGTGAT	2186
rs528653906	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67895306	CCACTGCACTCCAGC[C/T]TGGGTGACAGAGCAA	2186
rs528656844	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67887788	TAGGTCTACATATAT[A/T]TATGTGTGTTAACCT	2186
rs528667728	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67953346	CTGCAACCTCCTCCT[C/T]CCAGTTTCAAGCGAT	2186
rs528687641	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67944630	TAATGGTTATCTTGG[C/T]AACTATGCCCACACT	2186
rs528700368	snp	A/C	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67845031	TACAGGCATGAGCCA[A/C]TGCGCCCAGCCTGAT	2186
rs528725210	snp	C/T			upstream-variant-2KB	BPTF	GRCh38.p7	17:67824616	CTGAAACCTAGTGAC[C/T]TGTCAGGTCAATAAA	2186
rs528769256	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67937732	TATGGTCAGAGAGGT[A/G]GAGGGTGGGTGGGTA	2186
rs528777087	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67852426	TTATATGACCTCTTA[G/T]ATATATATATACCTT	2186
rs528780437	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67906675	CTCTTTCTTCAGCCA[C/G]ACCTTTCTGGAAGAA	2186
rs528786304	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67895835	GTTAAAAATGCAATT[C/T]GACTCCTTCCTAGTA	2186
rs528822456	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67945328	AGAATTCTCAACTTC[A/G]GAAGATTTCCTTCAG	2186
rs528835546	snp	A/C	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67841374	AGATTGCGCCATTGC[A/C]CTCCAGCCTAGGCAA	2186
rs528856052	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67890425	AGTGGCCAACTTCTG[A/T]TTTACACCCTTCCTG	2186
rs528866189	snp	A/G	0.0023933	0.0345097	intron-variant	BPTF	GRCh38.p7	17:67980174	ACATGGTAAAACCTC[A/G]TCTCTACTAAAAATA	2186
rs528894245	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67897089	TCCCAGCACTTTGGG[A/G]GGCCAAGGTGGGCAG	2186
rs528920216	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	BPTF	GRCh38.p7	17:67889854	AGACCCAAGAGAAAA[C/T]TGATAGTCTGACCAA	2186
rs528936195	snp	C/T	0.0325976	0.123435	intron-variant	BPTF	GRCh38.p7	17:67925709	GTTATACATAACTAT[C/T]TAAAAATCATATATA	2186
rs528963684	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67934090	AGGCTTTTTGGTGGA[A/G]AAGTAGTTCTTGAGT	2186
rs528971971	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67840763	AGATGGGGTTTCACT[A/C]TGTTGCCCAGGCTGG	2186
rs528981524	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67876851	TATTTATATGAAAAC[A/T]TAAGCAAGAAGTTTC	2186
rs528985078	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67874170	TGCGTACTGATATAC[C/T]GTGTGTTCTGTACAC	2186
rs528985198	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67848151	TTTTGAGGTCTAGAA[A/G]TCTGAAAACACTGTA	2186
rs529004217	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67981098	CTGGAGGTTGAGGCT[G/T]CAGTGAGCTGTGATT	2186
rs529035383	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67973696	TTTTTAGTAGAGACA[A/G]GGTTTCGCTGTGTTG	2186
rs529062196	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67854916	ATTGAAGGAATATGT[A/G]CATTAAAATAGCTTT	2186
rs529095897	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67954852	GGAAGAAGTTCAGTC[G/T]CTCTCTATAAATAGA	2186
rs529111912	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67855557	CCAACAGACTGAGGG[G/T]CATAGTCTGGCCTCA	2186
rs529144627	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67968262	GGCAGCATGAAAGAG[A/G]GGGAAACATGAAGTG	2186
rs529152322	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67939727	TTAAAACAAATACAA[A/G]AAATTAGTCGGGTGT	2186
rs529172388	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67948543	CTGAGAGGTGAGCTT[A/G]TTGATTGAATTGTTG	2186
rs529180686	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67861259	TGTCCCTCCGTGATA[C/G]AAGCCAGTGTCATCT	2186
rs529190295	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67851454	TTTTCCTCCACATGC[C/G]TATGCATAAGGATAG	2186
rs529205249	in-del	-/AT	0.00438332	0.0466095	intron-variant	BPTF	GRCh38.p7	17:67973078	ATAAATATATATATA[-/AT]ATATATATATATAAG	2186
rs529237700	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67955205	ATGGCATGAACCCGG[C/G]AGGCAGAGCTTGCAG	2186
rs529241097	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67917556	AACCACCATTTGGAT[G/T]CAGAATGTTTTTGTC	2186
rs529264000	snp	A/C	0.00755907	0.0610114	intron-variant	BPTF	GRCh38.p7	17:67867890	CCCCCAACCCCTCAA[A/C]CCCCCAATACTGTAC	2186
rs529301345	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67882042	ATTTCGCCATGTTGG[A/C]CAGGCTGGTCTCGAA	2186
rs529313217	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67868582	GGCTGACTATAGTGC[C/T]TTTTAAGTTTTAGCT	2186
rs529332854	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67972282	ACTCTGTCACCCAGG[C/G]TGGAGTGCAGTGTCG	2186
rs529356610	in-del	-/C			intron-variant	BPTF	GRCh38.p7	17:67940841	AACTACTAGAGTAAT[-/C]TTTAGACAGTGAGCT	2186
rs529356922	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67832732	TCTTCACCTCCCTCC[C/T]GCTCATCCCTGGCAG	2186
rs529360880	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67971022	CAGCTGACTGCATCC[A/T]CGTCCTCCCAGGTAC	2186
rs529387843	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67967015	TGAGGCAGGAGAATC[A/G]CTTGAACCAGGGAGG	2186
rs529398394	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67846008	TTCTTAAACTTTTTC[A/G]AAGCCAAAATTTTTC	2186
rs529410646	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67858069	GGGATTACAGGCGTG[A/G]GCCACCGTGCCCGGC	2186
rs529416721	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67978134	GCTGGGATTACGGGC[A/G]TGAGCCACCGCACCC	2186
rs529420416	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67943449	CAGTTCTGGACAGAA[A/G]AGAGAGCGCCTAGAG	2186
rs529436158	snp	C/T	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67881426	ATTGATCAACGAGTT[C/T]AGGTGGTGAGATTGC	2186
rs529455142	snp	C/T	0.00019799	0.00994766	intron-variant	BPTF	GRCh38.p7	17:67924624	CAGAGGACATCAAGG[C/T]CCAAATGGAGGCTCT	2186
rs529457378	snp	C/G	0.00398564	0.0444627	upstream-variant-2KB	BPTF	GRCh38.p7	17:67825321	TTTTGCCGCGCCACC[C/G]GCGCCCGGAGTCCAG	2186
rs529467832	snp	G/T	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67921124	CTGAGGCCCGAGAAT[G/T]GCTTGAGCCTGGGAA	2186
rs529470661	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67946523	TTAGATACATATAAT[A/G]TATAGTCAGTGCTTA	2186
rs529476262	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67839755	AAAGTTGTCCTAAAC[A/G]TTTCCATAATGGTTT	2186
rs529491998	in-del	-/A	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67981003	CCCTACAGAAAATAC[-/A]AAAAAATTAGCCGGG	2186
rs529495866	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67937861	GGCTCATGCCTGTAA[C/T]CCCAGCCCTTAGGGA	2186
rs529570256	snp	G/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	BPTF	GRCh38.p7	17:67889313	TTTGCACTAAATTTA[G/T]CAAGTGATAAAGGAT	2186
rs529592960	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67931609	GACTCCACATTTTCC[A/T]GTGAGCACTAGTTAC	2186
rs529602590	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67938716	TACAAGAGAACTTTA[C/T]AAGCAATAATTAAAG	2186
rs529605539	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67852718	ATATTTTGTACTTAA[A/G]TGAATGTGTGACTAC	2186
rs529607796	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67881653	GGACTATAGACGCGC[A/G]CCACCACATCTGGCT	2186
rs529636850	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67953062	GTCTCCCCGGGTTCA[C/T]GCCAGTCTCCTGCCT	2186
rs529657946	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67931085	TCCTGGTCAATATGG[C/T]GAAACCCTGTCTCTG	2186
rs529676253	snp	A/G	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67909248	GGCTGGAGTGCAGTG[A/G]CATGAGCCACCGCAC	2186
rs529676470	snp	A/C	0.00557542	0.0525036	intron-variant	BPTF	GRCh38.p7	17:67901315	TTGTTAAAAAAAAAA[A/C]AACCCAGAACCCTAA	2186
rs529767108	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67920499	TATGTAAGTGGGTCA[A/G]TAAAGGTTTCTTAAG	2186
rs529804174	in-del	-/A	0.00398564	0.0444627	intron-variant	BPTF	GRCh38.p7	17:67826460	CTCCCCCCCAAACAG[-/A]GGGGAAATGCGACGG	2186
rs529813560	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67902132	TGGCCTTGCTTCCTC[C/T]ACAAAGAGAAGCCTT	2186
rs529814478	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67840690	ACTTCAGCCTCTGAA[A/G]TAGTTGGGACCACAG	2186
rs529829962	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67957215	TTGAACCCAGGAGGC[A/G]GAGGTTGCTGTGAGC	2186
rs529839126	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	BPTF	GRCh38.p7	17:67823566	GCCTGACCACCCTCT[A/T]CAAACAAAATATGGG	2186
rs529846497	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67930057	GGAGGGGAAGGTTGC[A/C]GTGAGCTGAGATTGT	2186
rs529858264	snp	A/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67922307	TGCTTTTTATTTTTT[A/T]AATCTTTTTATGAGG	2186
rs529895123	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67958865	CCAGCTACTTGGGAG[A/G]CTGAGGCAGGAGAAT	2186
rs529900915	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67887567	CTTTGTTTTCAACCT[A/G]TCTGAAGTAATAATT	2186
rs529913716	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67830142	TAGGAAGTGTTTTCA[A/G]TAGGCATTTGGTAAG	2186
rs529920289	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67948387	TGCCTTTTTAATAAA[A/G]CTTAAAATTTCAGTA	2186
rs529936070	snp	C/T	0.00755907	0.0610114	intron-variant	BPTF	GRCh38.p7	17:67922056	ACAAAATCACAAGGT[C/T]GTCCTGGCACAGAAA	2186
rs529950234	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67868628	GGTAAGATTCTGAAA[A/G]TACACTTTTAAGTGC	2186
rs529965407	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67977095	GAAGAATAAATCTAA[A/G]AGTTTAAGAAAAAAT	2186
rs529971140	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67879448	CCCGGCTAGGGCTGG[C/T]GTTATTTCTTAAATG	2186
rs529984641	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67916442	TAAATATACAAAAAT[A/G]AGCCCGGCGTGGTGG	2186
rs530001908	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67941448	ACAAAGCAAGACTTC[A/T]TCTAAAAAAAACCAA	2186
rs530033384	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67872509	TCAGGAGTTTGAGAC[C/T]AGCATGGCCAACATA	2186
rs530064914	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67844190	GTTCAAGTGAGTCTC[A/G]TGCCACAGCCTCCGG	2186
rs530068860	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67900165	GCTAGAGGGCAGTGG[C/T]GCCATCTCGGCTCAC	2186
rs530089001	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	BPTF	GRCh38.p7	17:67983578	AGTGTAAACAGTAGC[A/G]AGAAAATGGAAACCA	2186
rs530097058	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67886788	AGTGATACATGGAGA[G/T]AATCTTTTTGTGTTA	2186
rs530132234	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67838035	ATAGGATGGACTAGA[A/T]GATCTAATGGTCAGG	2186
rs530165221	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67936563	TGTAGTTTCCAAACC[A/T]CTCTCTTCTCCAGGG	2186
rs530216540	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67851415	TGTGTGCACGTTCAA[A/T]TGAGTTCAGATTTAA	2186
rs530229003	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67976596	GAGGCTGTGACAGGA[C/T]GATCACTTGTGCCCA	2186
rs530283796	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67963555	TTAGGAAGCCAAATT[G/T]CTCTGACTGGTTACT	2186
rs530299225	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67943040	TGGCCTTATATATAC[C/T]TAAGATACATACCGA	2186
rs530323306	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67907484	CCTCAGCCTCCCAAA[C/T]AGCTGGGATTACAAG	2186
rs530342147	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67914595	ACTGGAAAAGTTACT[A/G]TGTACAAATACTTTA	2186
rs530344072	snp	C/G	0.0019968	0.0315343	intron-variant	BPTF	GRCh38.p7	17:67850891	TAGGGGAGAAGAAAA[C/G]ACACACACACAATAC	2186
rs530344953	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67898675	TCTTTTTTTTTTTTT[C/T]TGAAGATGTATTGCA	2186
rs530358639	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67951546	ATTCTACACAGAGTG[A/G]GAAAATAGTTGTAGT	2186
rs530374168	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67952356	GCAACCTCTGCCTGC[C/T]GGGTTCAAGCAATTG	2186
rs530388937	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67902989	AGTCTAATCCCCTAA[A/G]TGTAGAGCCTCACCA	2186
rs530391038	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67853831	TTTTAACTTGACAAT[G/T]ATTAAAGAAATGTAC	2186
rs530393181	snp	C/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67845324	CTGTTGATGGTTCTT[C/G]CTTGAATCAGTTACA	2186
rs530409236	in-del	-/AT	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67934065	AAGAAAAAAAAAATA[-/AT]ATAATTCATAGGCTT	2186
rs530424076	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67954048	CGGGAGTGCAGCGGT[A/G]CAATCACAGCACACC	2186
rs530425404	snp	C/G	3.62214e-05	0.00425551	missense	BPTF	GRCh38.p7	17:67945590	TCAGCCTGAAGTTCA[C/G]ACTCAGCCTGAAGTT	2186
rs530426004	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67864458	GCTTGAACCCAGGAG[A/G]CAGAGGTTGCAGTGA	2186
rs530433529	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67958227	TAGCTAGGTACTTGG[A/G]AGGCTGAGGTGGGAG	2186
rs530436558	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67932578	GTGCCTCATGCACCT[G/T]TAATCCCAGCTACTT	2186
rs530448681	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67910012	GCCTCATTCATACCC[A/G]TTAGCAGTTACTTCC	2186
rs530488439	in-del	-/T	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67964627	ACAAGAGTGTTAACA[-/T]TGACTCACTTCTTTA	2186
rs530495293	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67947592	TAGCTGCTAATTTTA[A/T]TTATGTTACGATATA	2186
rs530523788	snp	A/C	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67860530	CCATCTGAGAAGCCA[A/C]GACATATTCAGCATA	2186
rs530556024	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67946748	TCATTTGCATTTCTA[A/G]CCACACCTTTGTAAA	2186
rs530557053	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67902290	CCTCTCTCAGTGAAA[A/G]TGGCCCAGTTGCCAT	2186
rs530573535	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67833246	TATGGCTATACAGCC[-/T]TTTTTTTTTTTTTAT	2186
rs530632062	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67923213	GGTGCATGCCACCAC[A/G]CCCAGCTAATGTTTG	2186
rs530657896	snp	C/T	0.00279162	0.0372561	intron-variant	BPTF	GRCh38.p7	17:67965213	CCAGGTGCGGTGGGG[C/T]GCACCAGTAATCCCA	2186
rs530677008	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67960391	TATTTTTGTCAAAGT[C/T]TCCACTTTCTTATCA	2186
rs530696504	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67866933	CTGCTAGGCTGCAAA[A/C]CTGTACGTCATGTGA	2186
rs530700313	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67831834	CCTTCTCTTTGAGTG[C/T]CTGCTTACGGTGGTT	2186
rs530701737	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67925992	TAACCTAACATATTA[A/C]TTTTTTTTTTTTTTT	2186
rs530707851	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67917268	CTCCCAACTAGCTGG[G/T]ATTACAGGCGCCCGC	2186
rs530718906	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67873269	TCAAGACCAGCCGGG[C/T]CAACGTGGTGAAACC	2186
rs530747955	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67949163	TTGAGCCCAGGAGTT[C/G]AAGATCAGCCTAGGC	2186
rs530765434	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67867545	TTTCCTTAGTTTTTA[C/G]CTGATGTCCTTTTTC	2186
rs530767166	snp	A/G	0.0023933	0.0345097	intron-variant	BPTF	GRCh38.p7	17:67859501	ACTAAATCTCAAAGA[A/G]GTTAAATAATTTGCC	2186
rs530818448	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	BPTF	GRCh38.p7	17:67823675	CATTTGTCACCCTTA[A/G]AGCTCGACCAAATTG	2186
rs530824650	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67871228	GTACACAAAAGTTGA[A/G]AGAATTATACAGTTA	2186
rs530826795	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67909275	GCACCAGGTCCCCCC[A/C]CCCCTTTTTTTTTTT	2186
rs530826999	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67968656	AGCCGGGTGTGGTGG[C/T]GGGCACCTGTAGTCC	2186
rs530835859	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67866243	ACAAAGTACTCTCAC[A/G]TGGTTCTGAATTTTG	2186
rs530836185	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67873903	AAAAGAACAAAGGCT[C/G]CTTGGAGAGATGGTG	2186
rs530847285	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67933014	CCCAGCACTTTGGGA[A/G]GCCAAGGCAGGCCAG	2186
rs530850234	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67965186	CTCTCTACTAAAAAT[A/G]CAAAAAATTAGCCAG	2186
rs530881799	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67838668	TTTTTTTAGTAGAGA[C/T]GAGGTTTCACCAGCC	2186
rs530886455	snp	C/G	0.0023933	0.0345097	intron-variant	BPTF	GRCh38.p7	17:67930952	AGAGTGAGACTCTGT[C/G]TCAAAAAAAAAAAAA	2186
rs530922134	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67880178	TTCGTTACCTGCCCC[C/T]GTTAATCGTGTTGTG	2186
rs530922586	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67888326	GGGCTCGGTGGCTCA[C/T]ACCTGTAATCCCAGC	2186
rs530944354	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67839209	TAGTTATAACGATAG[A/G]CATCTTAGTATGCTT	2186
rs530956014	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67830866	CAGCCCTTTTTCACT[C/T]CTGAACACCCAGAGG	2186
rs531019798	snp	A/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67838165	GGAAAGCAGCCATAG[A/T]CAATAAGTAAACAAA	2186
rs531037494	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67906131	TCTGTCACCAGGCTG[C/G]AGTGCAGTGGCGTAT	2186
rs531042937	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67852392	ACTCTCCCCAGAAGC[A/G]AGTACTATAAAAAGA	2186
rs531056352	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67964722	ATAGTTGTTCTTGGC[C/T]GGGCATGGTGGCTCA	2186
rs531075446	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67936643	TTTGTATGATGAACT[A/G]CCCAACCCTGCCGCC	2186
rs531102190	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	BPTF	GRCh38.p7	17:67983740	TTGCACTAACTCATA[C/T]TAGCTTTGTCCTACC	2186
rs531110860	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67901143	ATAATTTGTTCTACA[A/G]AAGAAGCAAATCAGT	2186
rs531112887	snp	A/G	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67894392	AGCATGCAGTGGTGT[A/G]GTCTCGGCTTGCTGT	2186
rs531126733	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67939829	AGGTTGCAGTGAGCC[A/G]AGATCACGCCACCGC	2186
rs531126862	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67903416	AAGGAAAGATCTTCT[A/C]GTGTAATTATCCATT	2186
rs531127127	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67952469	GGTTTCACCATGTTA[A/G]CCAAGCTGGTCTTGA	2186
rs531159599	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67844203	TCGTGCCACAGCCTC[C/T]GGAGTAGCTAGCTGG	2186
rs531159984	snp	C/T	0.00358779	0.0422022	intron-variant	BPTF	GRCh38.p7	17:67907512	AAGTACCCGCCACCA[C/T]GCCGAGCTAATTTTT	2186
rs531164245	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67878146	ACTGGAACCATACAG[C/T]ATATACTCTTTGATG	2186
rs531170381	snp	C/T	0.00279162	0.0372561	upstream-variant-2KB	BPTF	GRCh38.p7	17:67823863	TGCCAGGCTGGAGTG[C/T]AGTGGTGCGATCTCG	2186
rs531184252	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67974940	GCCCCTCTCCCCTTC[C/T]GGAGGTTGGGGGATG	2186
rs531186011	snp	G/T	0.00279162	0.0372561	intron-variant	BPTF	GRCh38.p7	17:67872371	ATGGCACTGGGAAAG[G/T]AGGGAGGATGTACAA	2186
rs531191975	snp	A/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67970251	CAAAAAAAAAAAAAA[A/T]TTTAGCCAGGCATGG	2186
rs531245113	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67949287	GGATGATCACTTGAA[C/T]CCGGAAAGCAGAGGT	2186
rs531253451	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67969370	GGCACAAAAATCAGT[G/T]GAACCTGAGAGGCAG	2186
rs531258086	snp	C/G	0.00398564	0.0444627	intron-variant	BPTF	GRCh38.p7	17:67943676	GCCAGGGTACTTGAC[C/G]TTTCTAACCTGAGTT	2186
rs531266327	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67952925	TTATACCTTCATTAC[A/T]TCTTTGAATATATCA	2186
rs531287651	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67922190	ATCACTTCTCTTTGG[A/C]TTGTATCCCTTTGTA	2186
rs531295402	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67907099	CTGATGAGGGAGGAT[C/T]GTTTGAGCCCAGGAG	2186
rs531351972	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67921621	CTCCCCAAATGTATA[C/T]AATTAATTTTTGAAA	2186
rs531356556	snp	C/T	0.00358779	0.0422022	intron-variant	BPTF	GRCh38.p7	17:67843299	AGACATAGATACATA[C/T]AGATATATATCTACA	2186
rs531359251	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67836352	TATATTTTACTAGAA[A/G]TATGGCTTCTTGCTC	2186
rs531376497	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67978814	ATAAGGCTATGATTA[A/C]GCCAAAGAACGTCAG	2186
rs531388736	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67878817	AGGGTAAATCTGGTT[C/T]TTCCACTTTACCTTG	2186
rs531407835	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67935152	AACAAGACCTGATGC[A/G]GTGGCTCACACCTGT	2186
rs531421346	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67829444	GCTGCACTTACCGAC[C/T]GGCCCTCTAAGTTCC	2186
rs531423781	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67915514	TTTATTTTGGTACAG[C/T]GCATTCTGGCTTCTG	2186
rs531428536	snp	A/G			intron-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67919280	GTGGCTCTCACCTGT[A/G]ATCCTAGCACTTTGG	2186
rs531511365	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67975708	ACTTGTTAGAACTTC[A/G]GAGAATATTCACATT	2186
rs531532547	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67885027	TTTATGACTGTTCAC[A/G]TATTTTCCCATATTT	2186
rs531537389	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67942821	ACTATGCAGATGATT[C/G]TCACAAATATATAAT	2186
rs531595670	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67949458	CAGGCACCTGTAATC[C/G]CAGCTACTTGGGATG	2186
rs531617041	in-del	-/C	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67858636	CTGCCTGTCAGGGAG[-/C]CCGGTGCTTGTACTC	2186
rs531636296	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67905690	CTCGAGCCTGGATGA[C/T]AGAACCAGACTCAAT	2186
rs531674302	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67935874	AAAAAAGAATTTTGT[A/G]TAGGTATCCTTGTAG	2186
rs531677359	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67979334	ACGTGGATCATCTGA[C/G]ATCAGGAGTCGAGAC	2186
rs531677993	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67942166	ACTAAAAATACAAAA[A/G]TTAGTCAGGCGTGGT	2186
rs531701073	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67897603	GAGCTCCTTTTGGGT[G/T]GGGGGAAGGGTTGGG	2186
rs531703162	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67838007	TGGACCTCAGTTTAC[C/T]CACCTGTACAGTATA	2186
rs531704099	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67861960	TTTTAAAACACCCAT[C/T]CTACCAATAGTTTTT	2186
rs531726534	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67950239	GCCCTCCAACCTGGG[C/T]GACAGAGTGAGACTG	2186
rs531745230	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67919750	TCTGTCCTAGGCTTT[C/T]TATTATTTTGATTGA	2186
rs531758945	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67913347	CAGAAAGCTTCAAAA[C/T]TGGCCAACTAATGTA	2186
rs531835341	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67865139	TGAAAATCTGAAACG[C/T]TCCAATGAGCATTTC	2186
rs531836906	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67895481	TTTTTTTTTTTTTTT[G/T]GACACAGGATCTCAC	2186
rs531844884	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67956101	AGGCGGGCGGATCAC[A/G]AGGTCAGGAGATCGA	2186
rs531849237	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67862854	TAGCTTCTAGCACCC[C/T]AAGTGTCCTTGGCTT	2186
rs531868888	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67827232	TGAACTTCTGGAACA[A/T]CTTCTAAGTCACACG	2186
rs531873991	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67966829	AATTGTGGCCGGGTG[C/T]GGTGGCTCACGCCTG	2186
rs531874193	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67873729	ATACATATGTGCCCA[A/C]ACAAATAAATACAGA	2186
rs531875304	snp	A/G/T			utr-variant-3-prime, downstream-variant-500B	BPTF	GRCh38.p7	17:67983437	ACCAGGCAAATTACC[A/G/T]ATTACACACAGCTAC	2186
rs531901425	snp	A/G	1.6649e-05	0.00288518	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912707	TCAAGGTAGAAAAAG[A/G]CGATAAGCAAACTGT	2186
rs531917065	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67870156	CAACCTGCAGTTATC[A/C]TCTTAGTACTACATG	2186
rs531950053	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67919094	GGAGAATGGCGTGAA[C/T]CTGGGAGGCGGAGCT	2186
rs531961395	snp	C/T	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67965097	CTGTAATCCCAGCAC[C/T]TGGGGAGGCTGAGGC	2186
rs531981167	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67957309	AAAAATAAAAAAAAT[A/G]AAGGAAACGTGGGCT	2186
rs531992432	snp	C/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67958373	GAAGCTGGCCAAAAC[C/G]AAGATGGCGATGAAA	2186
rs531993441	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67963849	GTTAGAAAAACACTA[A/G]TTTGGGTACAAGCTC	2186
rs532007904	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67835811	GCTGGGACTACAGGC[A/G]CCTGCCACCATGCCC	2186
rs532010798	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67858602	CTGTGTTGTCATTGT[A/G]AGTGGAAATTCAGTG	2186
rs532019633	snp	C/T	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67839946	CCCTAGTACTTGATA[C/T]TGTCAGTTTTTTTTT	2186
rs532054903	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67951870	AGACCAGCCTGGCTG[A/T]CACGGCGAAACCCCA	2186
rs532071308	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67979421	GTGTGGTTGCACATG[C/T]CTGTAATCCCAGCTA	2186
rs532104022	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67907589	TCGAACTCCTGACTT[A/C]AAGTGATCTGCCTGC	2186
rs532104381	snp	C/T	0.00358779	0.0422022	intron-variant	BPTF	GRCh38.p7	17:67916387	CTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC	2186
rs532115178	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67872948	AAAAATTAGCCAGGC[A/G]TGGTGACACATACCT	2186
rs532133155	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67952496	TTGAACTCCTGACCT[C/T]AAGTGATCCTCCCTC	2186
rs532146358	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67895840	AAATGCAATTCGACT[C/T]CTTCCTAGTACAGTA	2186
rs532165758	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67915539	CTTCTGCCTTTTTCT[C/G]TCATGCCACCTTCAT	2186
rs532180189	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67865636	CAGGCTCACTCTCAT[C/T]GAGTGCCTCACACAT	2186
rs532232561	snp	A/G	1.64768e-05	0.00287021	missense	BPTF	GRCh38.p7	17:67975847	TGGCAGATATGACCA[A/G]AATTTTTGATAACTG	2186
rs532242011	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67908297	CCAAGTAGCTGGGAC[C/T]ACAGGCTCGTACCAC	2186
rs532251790	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67958786	CCTGGCCAACATGGC[A/G]AAACCCCGTTTCTAC	2186
rs532257330	snp	C/G	0.0023933	0.0345097	intron-variant	BPTF	GRCh38.p7	17:67837374	TTATACTCTCAACAT[C/G]TGTTTTTAAACCTTC	2186
rs532292950	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67871718	ACTTGTTGATAGAAT[A/G]TGCATATTTAGTATA	2186
rs532297177	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67976396	AAGAATCACTTGAAC[C/T]TGGGAGGCGGAGGTT	2186
rs532315670	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67829479	CCTTGCCCCCCACCC[C/G]CCGGATGTGACATTT	2186
rs532317866	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67837972	ACTTGAGTTTGGACC[A/G]TAGAGAAGTCATTCT	2186
rs532318557	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67879395	TCCACCCGCCTCAGC[C/T]TCCCAAAGTGCTGGG	2186
rs532325258	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67878931	TATTTTCCTTGTTAT[A/G]TATTATAGCATCCAG	2186
rs532353782	in-del	-/AA	0.00756509	0.0610354	intron-variant	BPTF	GRCh38.p7	17:67910622	CTGGCCAACATTGCG[-/AA]ACCCTGTCTCTACTG	2186
rs532360090	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67842261	GATATATATCTACAT[A/T]CATATACAATGCATG	2186
rs532381569	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67872435	GTGTTTGAAAATGGC[C/T]GGGCGTGGTGGCTCA	2186
rs532389617	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67893856	GTCAGCAGACAGGAC[A/G]TTAGAGGCATGAGTG	2186
rs532405872	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67885917	GGTCCTCACCCCCCC[A/C]AAAAAAGTCAGTGAG	2186
rs532427121	in-del	-/TT	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67953742	ACCATGCCCAGCTAA[-/TT]TTTTTTTGTGTATTA	2186
rs532432587	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67898756	ATTCAGGTGGAACAA[A/G]AAAGATACCCACTAT	2186
rs532470010	snp	A/G	0.00318978	0.0398085	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67886658	CAGTTACATTTATGT[A/G]TGTATGTTTACAAAG	2186
rs532485299	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67928917	ACTACGTTGCTGGTT[A/G]TTTTAAATCTAAAGC	2186
rs532494118	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67850849	AACATATTAAATGCT[C/T]TGCATTGTTCTGTGT	2186
rs532506254	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67896093	TCAGCCTCCCGAGTA[A/G]CTGGGACTATAGGCA	2186
rs532522505	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67913444	TCAGTTTTAACTTTC[A/G]TAAGACAAAAGGAAC	2186
rs532527912	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67951306	AGTCAATCATTAGCA[C/T]TAAAAAAAAATCTTA	2186
rs532529107	snp	A/C	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67921544	GTAAATAAATAAATA[A/C]ATAAATAAATAAAAA	2186
rs532567678	snp	A/C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67906891	AGTGAAGAAGGTAAA[A/C/G]AATAGGAAAATGCCT	2186
rs532583412	snp	A/C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67920498	ATATGTAAGTGGGTC[A/C/G]ATAAAGGTTTCTTAA	2186
rs532709723	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67957010	GAAACGTGCCCGGCA[C/T]GGTGGCTCACGCCTG	2186
rs532727224	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67863410	CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC	2186
rs532729217	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67963973	ATTGAATGTTTCATA[C/T]TTATCTTTAAATTGG	2186
rs532750908	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67884835	TTTGGGCTAGATTTC[C/T]AGACACAGGATTGCT	2186
rs532789652	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67864336	GTTCAAGACTAGCCT[C/G]GCCAACATGGCGAAA	2186
rs532804507	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67891397	AAAATTCATGACATT[A/T]ATGTTTATAAGCTCA	2186
rs532815668	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67981148	TGTGCTACAGAGTGA[A/G]ACCTTGTTTCAAAAC	2186
rs532842404	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67919827	TTTAGGAATTTGCAG[C/T]GAGGAAGAAGCTCAG	2186
rs532851500	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67870871	GCCTCCCGGGTTCAC[A/G]CCATTCTCCTGCCTC	2186
rs532868851	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67964593	CATATCCCCACACCA[C/T]GTCAGCTTATCTCAC	2186
rs532907190	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67855252	GCTGCAGTGAGCTGA[A/G]ATCACACCACTGCAT	2186
rs532909505	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	BPTF	GRCh38.p7	17:67981984	AATCTTTATTAGACA[A/G]ATATATATATATATA	2186
rs532924800	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67926255	CTCAAGCGATCTGCC[C/T]ACCAGGGCCTCCCAA	2186
rs532942778	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67848224	CAACTCTAAAAAATC[A/G]ACAGTGGTTTCTGGG	2186
rs532976326	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67836268	GATATGTTCTGTAAT[A/T]CACACGCTTGGGAAA	2186
rs532992375	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67878122	TGGTTTGCCTTTTTT[A/T]AAAAAATTACTGGAA	2186
rs533010393	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67904624	TGAAACTTGTTTGGT[A/T]AAAATGCATAAAACC	2186
rs533023131	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67926668	ATGCTTATTTATGAA[A/T]ATAGCTAACACTTCA	2186
rs533053142	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67974961	TTGGGGGATGGGACT[A/G]AAAGTCCCAACCCTC	2186
rs533060743	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67968198	TGAAAGAATTATGTT[C/T]CAAAAGCCAGCTAAG	2186
rs533072547	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67855589	TGTTCCTGAGGGTTT[C/T]GAGAAGCTCTTCTGG	2186
rs533104278	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67835827	CCTGCCACCATGCCC[A/G]GCTAATTTTTTGTAA	2186
rs533107996	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67856230	TTCCTTATCTTGGTC[A/G]TCCAACCCTGTTATC	2186
rs533113236	in-del	-/TAAG	0.0023933	0.0345097	intron-variant	BPTF	GRCh38.p7	17:67859791	TTAGAAAATCTAAAC[-/TAAG]TGGCAATTTCAGAAA	2186
rs533117981	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67905309	GCTACTGAGGAGGCT[A/G]AGGCAGGAGAATGGC	2186
rs533127978	snp	A/T	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67869359	GAACAAAGTCAAAAC[A/T]GGAATGGGTAATCAA	2186
rs533138735	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67956036	TAAAGACAGGGTCTC[A/G]GGCCAGGCGCAGTGG	2186
rs533150202	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67948657	GAGACAGTGAAGTAA[C/T]GTTGAAAGAATGAAA	2186
rs533172396	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67849101	GTTTCCAAAACCCTT[C/T]CTGCTTGGTAAGGGG	2186
rs533182962	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67843104	TACATATATCTATAT[A/G]TATGTAGATGTATGT	2186
rs533189750	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67862194	TTGGCCAGTCTGGTT[C/T]TGGACTCCCGACCTC	2186
rs533195452	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67973725	TGGCCAGGGTGGTCT[C/T]GGAACTCATGACCTT	2186
rs533200156	in-del	-/TTTTTTTTTTTTTT			intron-variant	BPTF	GRCh38.p7	17:67926009	TTTTTTTTTTTTTTT[-/TTTTTTTTTTTTTT]GAGACAAGGTCTCAC	2186
rs533220863	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67955394	GGGCACAGCAAACTC[C/T]ATTTCAGGTACAAAT	2186
rs533238133	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67941079	TACTGAAAGTTTATA[A/T]GGAGGTACAAAGTAT	2186
rs533247408	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67826788	GGATTTTTATTATAT[A/G]TCTGTTACTTAAAAG	2186
rs533250480	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67826394	CCTCTGCCCTCCCCC[C/G]TTGCTCACTCGTGTG	2186
rs533291275	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67949347	TCCAGGAAGCCGAGG[C/T]GGGTGGATCACGAGG	2186
rs533306910	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67840498	CTGCTCCTCCGCCTC[C/T]TCCTTCCCCTCCTCC	2186
rs533313446	snp	A/G	1.66479e-05	0.00288508	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911155	GGTGGAATTAAGGGT[A/G]TAGGAAAGACTTCTA	2186
rs533315971	snp	C/T	0.000798403	0.0199641	intron-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67918898	AAATCACAGGCCAGG[C/T]GTGGGCGCTCATGCC	2186
rs533317029	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67972297	CTGGAGTGCAGTGTC[A/G]TGATCTTGAATCACT	2186
rs533335701	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67886070	AATTGTCTTTTCTGA[A/C]AATTCGTCATTTTTC	2186
rs533338151	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67961240	ACACAGATACATGTG[C/T]CCATTCCATCGAGAT	2186
rs533349295	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67939528	ATGGAAAACTGTAGA[A/G]CCATTCCAGTTCAAC	2186
rs533378332	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67833815	TCAAGTGATCCACCC[G/T]CCTTGGCCTCCCAAA	2186
rs533406481	snp	A/G	0.00279162	0.0372561	intron-variant	BPTF	GRCh38.p7	17:67875804	TTCCCTTTTGTAGTA[A/G]AAGCCGAATGTCACC	2186
rs533448907	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67868059	TTTCTATGAGTATAC[A/G]TTCATGGATATTTTA	2186
rs533458266	snp	A/G	0.000399281	0.0141238	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911551	TCTAAACTAGCCAGT[A/G]CAGATGATATTGGTA	2186
rs533464026	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67947551	AGCACGGTACCCAGC[A/G]GGTGGTAAGCACCCA	2186
rs533480344	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67954938	ATAGTCTATAGACAG[A/G]AACAGATTCATTAAA	2186
rs533499227	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67831843	TGAGTGCCTGCTTAC[A/G]GTGGTTATGATCTCA	2186
rs533522967	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67969535	AAAATTCATATCATA[C/T]AGTGAATACATTTTC	2186
rs533525961	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67833043	ATCTTGTAATCCACT[C/T]GCCTCAGCCTCCCAA	2186
rs533555624	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67875086	AAATCTCCAGTTTTA[C/T]TTGCAAAATGAAAGT	2186
rs533572603	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67931741	CTTTCCTCAAAATTC[C/T]GTCTTTATTCTGATG	2186
rs533596287	snp	A/G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67877486	CTAAGAACAATAGCC[A/G/T]TGATAGAAGACATCT	2186
rs533606248	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67896343	GGAGCAACAAGTGTC[A/G]AGATTGAATCTCGTA	2186
rs533607124	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67869754	TTTGGGAGGCTGAGG[C/T]GGGCGGATCACGAGG	2186
rs533645739	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67924814	ACTATCACCCAGGCT[A/G]GAGTAGATCACAGCT	2186
rs533660029	snp	A/T			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67888410	TGGCCAACATAGTGA[A/T]ACCCTGTCTCTACTA	2186
rs533669315	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67862529	GTGGGATCGGGATTT[A/G]AACCTAGGCATTCTG	2186
rs533682846	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67861352	TTTCTTTTTTTTTTT[G/T]TTTTGAGATGGAGTC	2186
rs533684100	in-del	-/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67981244	AGGGAATTTCTATTG[-/T]TTTCCAGATTTAAGG	2186
rs533702050	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67882077	TGACCTCAGGTGATC[C/T]GCCCACTTCAGCCTC	2186
rs533708337	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67830685	ACTGATAGTAAAGTG[G/T]GGGCAGTCTCAAGTA	2186
rs533708940	snp	A/T	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67923864	TTTATTTTATTTTAT[A/T]TTTGAGACAGTTTCA	2186
rs533722586	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67974068	TTGGTTGAACTTCCA[A/G]ATCACTTTCAAATTC	2186
rs533751822	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67962972	TGACAGATGTAAGTC[G/T]TTGATTCTTTGGCTT	2186
rs533798694	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67907825	CAAATTAACCGTAAT[C/T]AACAAATTAATAATC	2186
rs533801380	snp	A/G	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67883016	TAAAAAAAAAAAAAA[A/G]AAAAGAAAAGAAAAA	2186
rs533809920	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67856542	TAGCCAGTTGGAAGC[G/T]CTGAGCAAGTGGGTG	2186
rs533829810	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67968264	CAGCATGAAAGAGGG[A/G]GAAACATGAAGTGGA	2186
rs533862320	snp	C/T			upstream-variant-2KB	BPTF	GRCh38.p7	17:67824367	CTCTTGACCTCAAGC[C/T]ATCATCCGGCCTTGG	2186
rs533863218	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67883664	GAGTGCAGTGGCACG[A/G]TCTTGGCTCACAGCA	2186
rs533906311	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67847417	TACTCGGGAGGCTGA[C/G]GCAGAAGAATAGCGT	2186
rs533935069	snp	G/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67948007	GTCTCATCTGTAGAG[G/T]CATAGAAGAATGATG	2186
rs533936774	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67835411	AGGGGGAATTTACCT[A/G]ACATCTCTTTTTCTC	2186
rs533964906	snp	C/G	0.0023933	0.0345097	intron-variant	BPTF	GRCh38.p7	17:67841057	TTCTTTTACACATCT[C/G]GGGTTCGTCTAACAA	2186
rs533971011	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67933839	CGAGATGGGCAGATC[A/G]CCTGAAGTCAGGAGT	2186
rs534023610	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67979860	AGCCTGGCCAACATC[A/G]TGAAACCCCGTCTAC	2186
rs534026099	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67890633	TGATTTGCAGCCCTG[A/G]CAGAATCATATGATT	2186
rs534031214	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67855068	CACTTTGGGAGGCCA[A/G]GGTGGGTGGATCACC	2186
rs534034548	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67829436	GGTGGCTTGCTGCAC[A/T]TACCGACCGGCCCTC	2186
rs534093358	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67841534	TTTTTCTACCCTTTT[A/G]CTTTTAATTTATATA	2186
rs534094038	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67881467	GTTAACCTCTCACTC[A/G]TTAATAATCTTTCCA	2186
rs534105519	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67860981	CTTACTGACTTCCCG[G/T]GCCTGAATTCCTTCT	2186
rs534110803	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67967175	TGAGACGATGTCTTG[C/G]TTTGTCGCCAGGCTG	2186
rs534110871	snp	A/G	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67960701	GATTGTGCTTTAAAA[A/G]CTGATCATTTAGAAT	2186
rs534163278	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67861606	CAGATGTGAGCCACC[A/T]TGCCCAGCCATAGCT	2186
rs534165722	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67916461	CCGGCGTGGTGGCGG[A/G]CGCCTGTAATCCCAG	2186
rs534169030	snp	A/G	1.83832e-05	0.00303171	intron-variant	BPTF	GRCh38.p7	17:67966702	CAGAAGTCTCAGTGG[A/G]TGTTTTATTATCCAT	2186
rs534200654	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	BPTF	GRCh38.p7	17:67825434	GCGCCGCTTCGCTCC[C/G]TCCCAGGCTCGTCGG	2186
rs534241540	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67868208	GTTTAAATAGTATAA[A/G]GGGTATGCTGTGAAA	2186
rs534243227	snp	A/G	0.00597247	0.0543191	intron-variant	BPTF	GRCh38.p7	17:67961350	TATTTTAGTTGAGAT[A/G]AGTTAGTGTTTCTAA	2186
rs534272860	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67832437	CTATTATTTTGTGAT[C/T]GTCACATTTTAAAAA	2186
rs534294815	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67843266	TATATCTACATATAT[A/G]GATACATATAGATAT	2186
rs534294897	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67979107	CCCATGAGGTAGACG[C/G]TGCAGTGAGCCATCT	2186
rs534318637	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67948915	GAGCCTGGCAGGTTG[A/G]AGCTGCAGTCAGCCC	2186
rs534318963	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67939842	CCAAGATCACGCCAC[C/T]GCACTCCAGCCTGGG	2186
rs534330539	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	BPTF	GRCh38.p7	17:67824872	CCTCCCTCCGGGCGT[C/G]GCAGCCCGGGGCGTG	2186
rs534414309	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67867819	GTGACTTACCACTGA[C/T]GATGTTAACCTTGGT	2186
rs534418124	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67839470	AATTATATTAGATCT[C/T]ATAATATTGATCCAC	2186
rs534430172	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67972430	TTTTTAGTAGAGACG[G/T]GGTTTCACCATGTTG	2186
rs534437250	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67952640	CCCCACCCACACACA[A/G]TTTCCCCTATTAATG	2186
rs534445219	snp	C/T	1.7895e-05	0.00299118	intron-variant	BPTF	GRCh38.p7	17:67931863	AAGTCCATTATACTT[C/T]AATCTTTTTAAAGCA	2186
rs534458248	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67932750	TTTTTTTAAACCCTA[G/T]ACATTTATGAGAAAT	2186
rs534482697	in-del	-/TAGATACATATAGATATCTACATACATCTACATACATGTAGATGTATG			intron-variant	BPTF	GRCh38.p7	17:67843167	ATATATCTACATATA[lengthTooLong]TAGATATATACCTAT	2186
rs534528100	snp	C/T	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67909407	TAGGTCAGCCAGGCA[C/T]ATAGGATTATATGGT	2186
rs534546555	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67910617	CCAGCCTGGCCAACA[C/T]TGCGAAACCCTGTCT	2186
rs534547988	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67828263	AATAATTTTTACCTT[A/G]AGAAATCACATGTTG	2186
rs534553258	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67845373	GACTTCTCTATTTCT[A/G]TCATTTCTTTGTTAA	2186
rs534554043	snp	C/T	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67918482	ATATGGCATTTAAAA[C/T]GAATATAGCCCCTTT	2186
rs534562377	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67938105	GCGAGACTTCACAGA[A/C]CCTCGGAGTACAGTC	2186
rs534588889	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67905484	GGCTGAGGCAGGAGG[A/C]TCACTTGAGGCCAGG	2186
rs534601695	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67874212	TGTATCCCGTGGTCT[A/G]TAACATGCCATAGTA	2186
rs534609663	snp	G/T	0.00279162	0.0372561	intron-variant	BPTF	GRCh38.p7	17:67896021	CAGGCTGGAGTGCAG[G/T]GGCGTGATCTCGGCT	2186
rs534697254	in-del	-/T	0.00676609	0.0577691	intron-variant	BPTF	GRCh38.p7	17:67964794	CACAAGGTCAGGAGA[-/T]TCAGACCATCCTGGC	2186
rs534709384	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67916027	ATATTTATTTGCTTT[C/T]TCCTGTGACACTAAA	2186
rs534716781	snp	A/G	0.0023933	0.0345097	intron-variant	BPTF	GRCh38.p7	17:67871643	GTAGAGATGGCTTCT[A/G]AAACCTGGTAGGTTA	2186
rs534726492	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67841269	AAAAAATTAGCCGGT[C/T]GTGGTGGCACATGCC	2186
rs534733891	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67904073	TCGCTCTGTTGCCCA[C/G]ATTGGAGTGCAGTGG	2186
rs534738442	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67881651	CAGGACTATAGACGC[A/G]CGCCACCACATCTGG	2186
rs534753068	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67880437	CAGCTTTCCTCTATG[C/T]CCTGCTATAGCTACA	2186
rs534768796	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67933784	TAGGCTTAACCCAGG[C/T]GCAGTGGCTCATGCC	2186
rs534775355	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67895608	GTTGGGACTACAGAC[A/G]CATTCCACTATGCCT	2186
rs534782897	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67853348	ATTCTTCTCTTTTCT[C/T]CTCCTCTGCACTTCC	2186
rs534790688	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67844900	AGGCATGTGCCACCA[C/T]GCCTGGCTAATTTTG	2186
rs534813629	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67901001	TGCATCCTGGGCAAC[A/C]GAGTGACAACCTGTC	2186
rs534828223	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67873286	AACGTGGTGAAACCC[C/T]GTCTCTACTAAAAAT	2186
rs534837968	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67901609	AACAAGACAAAGGAT[C/T]TGAATAGGCATTTTG	2186
rs534847380	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	BPTF	GRCh38.p7	17:67823854	TTGCTTTGTTGCCAG[A/G]CTGGAGTGCAGTGGT	2186
rs534861418	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67953152	ATTTTTAGTAGAGAC[G/T]GGGTTTCACCATGTT	2186
rs534927798	snp	A/C	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67852804	ATGTTTGCCAAATTA[A/C]CTTCTAAAAATCCAA	2186
rs534937456	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67894618	CAGGTGTGAGCCACC[A/G]CACCCACCATGAATA	2186
rs534940775	snp	A/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67976079	AATATCTTTAAAAAA[A/T]AAATAAATAAATCAA	2186
rs534953735	snp	C/T	0.000150014	0.00865935	intron-variant	BPTF	GRCh38.p7	17:67886331	GGTAAGAATATACTT[C/T]ATCCATTCCTTTAAA	2186
rs535015929	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67886961	ATCCTTAACGTATAT[C/T]TTTGTGTACTTGTGC	2186
rs535017479	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67849944	AGACTCCATCTCAGA[A/C]AAAAAAAAATTCAGG	2186
rs535044085	snp	C/T	0.0064421	0.0563875	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67826071	TGGCCCGGACCACCG[C/T]GGCCCGGAGGGCCGT	2186
rs535066742	in-del	-/TA	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67845372	TGACTTCTCTATTTC[-/TA]TCATTTCTTTGTTAA	2186
rs535086948	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67924244	ACAGGCATGAGCCAC[C/T]GCACCCGGCCTGAGC	2186
rs535099912	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67830946	ATATCAAATCACAGA[G/T]ATGCTGTTGAACCAC	2186
rs535127310	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67959025	TTGCACTACTCTCCC[A/T]GCAGTCTGAAATTCT	2186
rs535165514	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67882295	GGATACTTTTTGTTG[C/T]TGGGCTCTCACTGTC	2186
rs535190329	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67833210	CATGTATCAGTACTA[C/T]ATTTGAATAACACTT	2186
rs535191829	snp	A/G	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67976871	AAGCCCCTGCACTCT[A/G]TGAGGGGTGGGTGGA	2186
rs535212698	in-del	-/AAAAAAAAAAAA	0.493881	0.054972	intron-variant	BPTF	GRCh38.p7	17:67921210	TTGAGAATCCGTGTC[-/AAAAAAAAAAAA]AAAAAAAAAAAAAAG	2186
rs535246993	snp	A/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67830282	CTTACCTGGAATTTT[A/T]AAACTTGGAACCTCT	2186
rs535293350	snp	G/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67903159	GGCCCCTTTCTCTGC[G/T]GATGTAAGAAACCTG	2186
rs535297603	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67952267	TTTTTTTAATAGGCT[-/T]TTTTTTTTTTTTTTG	2186
rs535335475	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67970593	ACCTAAATGTGTTTA[G/T]AAATGCATAGAAAAT	2186
rs535360844	snp	A/G	4.34811e-05	0.00466247	intron-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67929531	TGATGTGTTGAGCAC[A/G]TCACATTATTTTTAG	2186
rs535382589	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67834244	ATCCTTCTGTTACTG[A/G]TTTCTAATTTAATTT	2186
rs535386261	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	BPTF	GRCh38.p7	17:67889534	ATCTGAAGGCCAGGC[A/G]CAGTGGCTCACGCCT	2186
rs535401295	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67922602	GCAAACCACAGCCCA[C/T]GAGCCTTGGCCTACC	2186
rs535413415	snp	A/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67973077	ATATAAATATATATA[A/T]AATATATATATATAA	2186
rs535415524	snp	A/G	0.0182019	0.0936463	intron-variant	BPTF	GRCh38.p7	17:67955863	AAATTATCATTTATA[A/G]GCCAGGAGAGGTGTG	2186
rs535431399	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67875918	TTTGATAAATGTCCT[C/T]GCAGTTAGTGCTTGA	2186
rs535433701	snp	C/T	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67868344	TTAATAAATACCACC[C/T]GTGTTTTCTAATGTA	2186
rs535434727	snp	G/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67909481	TGAAAAAATGAAACA[G/T]AACTTGCTGGAAATT	2186
rs535454336	snp	A/G	0.0023933	0.0345097	intron-variant	BPTF	GRCh38.p7	17:67935316	CCTGTGGTTTCAGCC[A/G]CTTGGGAGGCTGAGG	2186
rs535476776	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67979583	TGGTTTTCGACTTTT[A/G]GAATCACCCTATAGA	2186
rs535544823	in-del	-/C			intron-variant	BPTF	GRCh38.p7	17:67864955	GACGACAGGCGCCTG[-/C]CACCATGCCCGGCTA	2186
rs535561868	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67882842	CAAAATTCCTTTTCT[A/G]TAAAAATTAGCTGGG	2186
rs535570519	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67875417	ATTGCAGCAATATCC[G/T]AGAATCTACTTGCTT	2186
rs535590946	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67867079	TGGTTCCTGGTGGAC[C/T]GAAACATTGTGCAGT	2186
rs535593667	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67878546	CATCCTTGCTAACAC[C/T]GGGTATCATCAGCAT	2186
rs535597318	snp	C/T	0.00398564	0.0444627	utr-variant-3-prime	BPTF	GRCh38.p7	17:67983002	AACAGTACAATTTGT[C/T]AATTACTCTGCACCA	2186
rs535613581	in-del	-/GTACAGTAGAGAGACTTTTACCCTGT	0.0119091	0.0762411	intron-variant	BPTF	GRCh38.p7	17:67895848	TTCGACTCCTTCCTA[-/GTACAGTAGAGAGACTTTTACCCTGT]GTACATGAGAAGACA	2186
rs535619456	snp	A/G	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67957999	CCACTAGATAGCAGA[A/G]GAGGTGTGCTTAAAA	2186
rs535621341	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67965931	CTGCACATGTTGGCA[C/T]GCACTTGTAATCCCA	2186
rs535625548	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67934007	TGAGACCCTGCCATT[A/G]CACTCCAACGTGGGC	2186
rs535628659	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67938323	AAACTGCAATGCAAG[G/T]ACATAGCACTGGGAT	2186
rs535634856	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67831214	CACTTTAGAGTTCTT[C/T]AGGCCTTGACACATA	2186
rs535683785	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67901392	TTGTTGTGATACTTT[A/C]TTTTTAAACAGATAA	2186
rs535686711	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67977439	AGAATCGCTTGAACC[C/T]GGGAGGCACAGGCTG	2186
rs535711820	snp	A/G/T			intron-variant	BPTF	GRCh38.p7	17:67964776	GAGGCCAAGGTGGGC[A/G/T]GATCACAAGGTCAGG	2186
rs535737484	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67853085	AGGTCGCAGTGAGCC[A/G]AGGTCACGCCACCAT	2186
rs535753142	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67845738	TGATAGCACCACTGC[A/T]CTCTAGCCTGAGCGA	2186
rs535763913	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67838882	TTGTGTATAAAAATA[A/C]CTGCTCTGCTGGGGC	2186
rs535770918	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67880578	AATATGGTGTGTGAT[G/T]AAGTATATTGCTTAA	2186
rs535780506	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67971660	AATACCAAAATTAGT[C/T]GGGCATGGTGGTGTG	2186
rs535803256	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	BPTF	GRCh38.p7	17:67983948	TGAAGCCCATTCCTT[C/T]TTGTACATAAAGATG	2186
rs535809748	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67844348	TATCTCCTAGGTTCA[C/T]GCCATTCTCCTGCCT	2186
rs535836228	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67959951	TTTGAAGAAAATGAA[C/T]ATTTTGGGAGTGATA	2186
rs535869448	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67863187	TTTCAAAGAGAATCT[A/G]TTCCATGCCTGTCTC	2186
rs535911894	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67954320	TTACAGGCATGAGCC[A/T]CCGTACTCGGCCCTG	2186
rs535936751	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	BPTF	GRCh38.p7	17:67984496	TGAAACCAGGAAGAT[A/G]TTAATTTCATATGTG	2186
rs535941101	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	BPTF	GRCh38.p7	17:67824595	TGATTCGTCCTTTGG[A/G]CTAAGCTGAAACCTA	2186
rs535963960	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67895485	TTTTTTTTTTTTGAC[A/G]CAGGATCTCACTGTC	2186
rs535976687	snp	C/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67953786	GGTTTCATCATGTTT[C/G]CCAGGCTTGTCTCGA	2186
rs535996180	snp	C/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67944819	GGAGAAAAGTGAAGC[C/G]TGGCAATTAGCCTGG	2186
rs536013118	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67883820	TGGCCAGGCTGGTCT[C/T]GAACTCCTGAGCTCA	2186
rs536014820	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67857593	TGCTTCAGCCCACCA[A/G]GTAGCTGGGACTACA	2186
rs536018090	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67971148	CAGTGGCGCTATCTC[G/T]GCTCACTGCAACCTC	2186
rs536039137	snp	C/G			downstream-variant-500B	BPTF	GRCh38.p7	17:67984487	ATGGAAATCTGAAAC[C/G]AGGAAGATGTTAATT	2186
rs536040179	snp	C/T	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67964818	TCCTGGCTAACACGG[C/T]GAAACCCCGTCTCTA	2186
rs536080332	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	BPTF	GRCh38.p7	17:67823949	GAGTAGCTGGGACTA[C/T]AGGCACGCACCACCA	2186
rs536095980	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67858128	GAAGGTTTCAGGAGG[G/T]AACAAAATGAAATCT	2186
rs536126366	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67916598	TCCGTCTCAAAAAAA[A/T]AATAATAATATACAA	2186
rs536129997	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67866096	ACTGCACTCTAGCCC[A/G]GGCGACAGAGTGAGA	2186
rs536133681	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67923334	AAGTGCTGGGATTAC[A/G]GGCATGAGCTACCCT	2186
rs536141992	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67838735	TCCTCCTTGGCTTCC[C/G]AAACTGTTGGGATTA	2186
rs536158821	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67965403	AGTGATAGAGATATA[C/T]TGAAGACATAGAAAG	2186
rs536160677	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67958456	AAAGGGGCCAGGCAG[C/T]GTGGCTCACACCTGT	2186
rs536176688	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67899020	ATATAGACACAATTA[C/T]TATATGCAGTTGATC	2186
rs536197372	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67922771	CCACTTTTTCATGAT[A/T]GAAGATGCCAGAAGT	2186
rs536200843	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67915738	TCTGATCCTCATTCC[A/C]GAGCCAACTCAGATG	2186
rs536203150	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67837447	GAGTCTTGCTCTGTC[A/G]CCCAGGCTGGAGTGC	2186
rs536206250	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67829064	AATCTCTAAATACTT[C/T]GGATTTAGGAAACTA	2186
rs536226902	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67958269	CCTGGGAGGTGAAGG[C/G]TACAGTGAGCCAAGA	2186
rs536227285	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67968899	AGGCGGAGAATTGCT[G/T]GAACCTGGAAGGCAG	2186
rs536239916	snp	C/T	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67871216	AAAATTTCAAATGTA[C/T]ACAAAAGTTGAAAGA	2186
rs536240788	snp	A/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67943966	AACTCTGGATTGTTG[A/T]TGTTTTTCCTACTAA	2186
rs536245028	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67887165	CTTAACATTTTTGCC[A/G]ATGGTGAAAAGTATT	2186
rs536252416	snp	A/C	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67936122	TATAAAACATGGTTC[A/C]AGGGCATAAGGGGAA	2186
rs536272057	in-del	-/ATCTACATACATGTAGATGTATGTAGATATATACCTATAT	0.0905309	0.192535	intron-variant	BPTF	GRCh38.p7	17:67843192	TAGATATCTACATAC[lengthTooLong]ATCTACATACATGTA	2186
rs536276764	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67900724	AAAAGTTAATGTGCA[A/G]GAATACTGCACACAG	2186
rs536296225	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67918051	TGATCTGCCCACCTC[A/G]GCCTCCCAAAGTGCT	2186
rs536321476	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67929737	GCTTTCTAGGATTTT[A/G]TAAAGAAAATTTCTT	2186
rs536375594	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67886040	AAATACAGCTTCTTA[A/G]TGAAATCCTAAAACA	2186
rs536390853	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67928174	CAGGTGTGAGCCACC[A/G]CAGCCAGCCATAAAT	2186
rs536408113	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67842526	CCAACTTTCTGTGCT[C/G]TCCCAGATAAACTCC	2186
rs536461391	in-del	-/A	0.00279162	0.0372561	intron-variant, utr-variant-3-prime	BPTF	GRCh38.p7	17:67981638	AATGTATTTAAAAAT[-/A]TGTAAACTCTTGGAA	2186
rs536466321	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67900748	CACACAGTAGCTCAC[A/G]CCTGTAATCCCAACA	2186
rs536470733	snp	C/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67898109	ATGCAGTGGCTGACA[C/G]TTGTAATCCCAGCAC	2186
rs536473253	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67906516	TGAGCCGATTATTTC[A/C]CGAGGGTGCCAGGTG	2186
rs536495846	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67964741	CATGGTGGCTCATGC[C/T]TGTAATCCCAGCACT	2186
rs536502761	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67871887	CTGGAGTGCAGTGGC[A/T]TGATCTCGGCTCACT	2186
rs536516727	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67935419	GGTGACAGAGTGAAA[A/C]CCTGTCTCAAAAAAA	2186
rs536537060	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67907777	CTCTACGTAGACATT[G/T]TTCCATAACCATCAT	2186
rs536606427	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67839035	TGTCATCTGCAAAAA[G/T]GAATCATATGTACAC	2186
rs536678099	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67975344	AGCAAAATGATGTTA[C/T]TAAAGTCTAATACCA	2186
rs536678659	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67869039	AAGTAATTGCAGTAA[A/C]ACAATCTCCGTCTTA	2186
rs536687572	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67925701	TTAACATAGTTATAC[A/G]TAACTATTTAAAAAT	2186
rs536711500	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67931245	ACTCCAGCCTGGGCG[A/G]AAGAGCGAGATTCTG	2186
rs536729282	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67921784	CGCCTGTAATTCCAG[C/T]GCTTTGGGAGGCCAA	2186
rs536736082	snp	C/T	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67971230	ATTACAGGCATGCGC[C/T]ACCACACCCAGCTAA	2186
rs536740060	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67978218	ATCTTGAACTCCTGA[A/G]CTCAAGCGATCCTCC	2186
rs536771309	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67878555	TAACACTGGGTATCA[C/T]CAGCATCACTCTTTG	2186
rs536772247	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67937908	TCACCTGTGGTCAGG[A/G]GTTCAAGACCAGCCT	2186
rs536792601	snp	A/G			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67888342	ACCTGTAATCCCAGC[A/G]CTTTGGGAGGCCAAG	2186
rs536802315	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67908638	GGGATCACAGTTGCA[C/T]GCCACCATGCCTGGC	2186
rs536816343	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67858779	TTAGTCCATGCTCCA[A/G]TTCTCCCATTCCTGT	2186
rs536822374	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67958936	TGCACCATTGACAAG[A/T]GCGAAACTGCATCTC	2186
rs536861330	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67903106	ATGGGCCGACCTTCC[A/T]CATCCTTCCTCTCTT	2186
rs536876248	snp	A/C	0.0799831	0.183287	intron-variant	BPTF	GRCh38.p7	17:67843197	ATCTACATACATCTA[A/C]ATACATGTAGATGTA	2186
rs536937115	in-del	-/GAA			intron-variant	BPTF	GRCh38.p7	17:67936004	GACATATCAACAGAA[-/GAA]ATTTGAAAAGTTGCC	2186
rs536939105	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67901462	ATTTAAAATTCTGAG[C/T]GGAAAAATGTTATTG	2186
rs536940351	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime	BPTF	GRCh38.p7	17:67982518	ATCAGATGGTTTTAC[A/T]ATTGTGGCAGAAGCG	2186
rs536948436	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67857031	CCTTCCTTTTTAGTT[A/T]GAGATCAGGCTTTCT	2186
rs536960655	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67870280	TTTTTTTTTTTTCGG[C/T]TAAGGTACAACATCA	2186
rs536961948	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67944035	TGCTGGTGACATTCA[A/G]ATATGTATTTTCATT	2186
rs536962018	snp	A/G	0.00279162	0.0372561	intron-variant	BPTF	GRCh38.p7	17:67953098	TCCCGAGTAGCTGGG[A/G]CTACAGGCGCAGGCT	2186
rs536982911	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67942439	ATTAAAACCATATGC[C/T]TAAGAGATTGGTACA	2186
rs537004126	snp	C/G	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67830244	TGTTGCAGTCTCAGT[C/G]TTGTGTGAGACTTCT	2186
rs537004577	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67977619	GAGGCCGAGGCGGGC[A/G]GATCACGAGGTCAGG	2186
rs537013518	snp	C/T	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67964766	AGCACTTTGGGAGGC[C/T]AAGGTGGGCGGATCA	2186
rs537045757	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67880663	TGTGTGTAAGACAGG[A/G]TCTTGCTCTGTTACC	2186
rs537064265	snp	A/G	0.000798403	0.0199641	downstream-variant-500B	BPTF	GRCh38.p7	17:67984591	TTCATCAACTACAGA[A/G]CTTTAGTCCTTCAGA	2186
rs537068147	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67831466	TATGCATTAATAAAT[A/G]GTCTTGCACACAGTT	2186
rs537078033	in-del	-/TAATAATAATAATAATAA			intron-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67919203	TAATAATAATAATAA[-/TAATAATAATAATAATAA]AATATAATGCTTGTT	2186
rs537169788	snp	A/G			intron-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67929572	TCCAAGATTAATCCA[A/G]CTCAGTTTCCTTTGC	2186
rs537186952	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67930624	CTATAAAACTGAAAA[G/T]AAAATACTTTCTAGT	2186
rs537190705	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67915184	TCATACACTCAATAG[C/G]GCCTCTTTTTCCCTC	2186
rs537203417	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67900785	GAGGTTGAGGAGGGA[A/G]GATCACCTGAAGTGA	2186
rs537222179	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67851997	GTTGAAATTGATAAT[A/G]AGTGTAATGCTCAGT	2186
rs537227781	in-del	-/AATGAGTTG	0.00478085	0.0486577	intron-variant	BPTF	GRCh38.p7	17:67893817	GAAAACGTCATTACC[-/AATGAGTTG]AATGAAGTCAATGTG	2186
rs537237546	snp	A/C	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67935502	ACAAAACAGAAAAGA[A/C]CAAAAAAATTAGACC	2186
rs537264563	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	BPTF	GRCh38.p7	17:67982541	CAGAAGCGAGAAAAC[C/T]TTGTTTATTGAAAAA	2186
rs537274264	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67892588	GTCCCAACTTTGTCT[C/T]CCATATTCGAGAATT	2186
rs537277638	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67845590	ACCAGCCTGGGCAAT[C/G]TAGGGAGACCCCATC	2186
rs537291549	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67958541	AACACCAGCCTAGCC[A/G]ACATAATGAAACTCT	2186
rs537299671	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67958591	AAAATTAGCTGGGTA[C/T]GGTGGTGGGTGCCTG	2186
rs537316074	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67958721	AGGCAACAAAGCACT[C/T]TGGGAGGCCGAGGCG	2186
rs537325162	snp	G/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67908063	TCCATTTCTAATAGG[G/T]TTCTGTGACACAAAG	2186
rs537334473	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67894801	TAGGAATCTGATTTA[C/T]ATCTGTTTTTAAAGT	2186
rs537347687	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67850961	TGCAGATATAATAAA[C/T]AAATGATATAATAAG	2186
rs537351777	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67874540	ATATCTATATCAAGG[A/C]TATATTTTAAAAAGA	2186
rs537359527	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67858177	CTGCTGTGAGAAACA[A/G]TACTTAAGGTTTTAA	2186
rs537384498	snp	A/G	0.00597247	0.0543191	intron-variant	BPTF	GRCh38.p7	17:67957074	GATCACCTGAGGTCC[A/G]GAGTTCGAGACCAGC	2186
rs537426070	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67944868	TTTCCAGAGGCTGCA[A/G]CTTACTTTGGAAACC	2186
rs537460966	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67906093	GGAGGGGTTGTTTTT[A/G]TTTTTTTGAAATGGA	2186
rs537472062	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67976833	GTGTGCCTGATACTG[A/G]GAATTTAGCAGTGAA	2186
rs537472369	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67969807	GTCTTTACAAAAAAA[A/C]AAAAAATGCTCAGGA	2186
rs537491082	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67865745	CCTGTTTGTTTTAAG[C/T]TAGTGACCATCTCTG	2186
rs537493830	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67942504	AGACATAGAGCAGAA[A/G]GAATTCTCATGCACA	2186
rs537514985	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67942748	CAAAATCAGTTAGCT[A/G]AGTAAATTGTAGTAT	2186
rs537547459	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67829623	GAGGAAGGCTGTCAG[A/G]TAAATGTGTAGATAG	2186
rs537555418	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67964829	ACGGTGAAACCCCGT[C/T]TCTACTAAAAATACA	2186
rs537566493	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67871977	ATTACAGGCGTGTGC[C/T]ACCACACCTGGCTAA	2186
rs537609518	snp	A/C	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67968356	TGATGTTGAAAATAG[A/C]AGGAGTTAATCATTG	2186
rs537630986	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67943067	CCGAAGTAGTAATGA[A/T]ATACAGTGTTATCAT	2186
rs537681777	snp	A/G	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67837649	TGCTGACCTCAGGCA[A/G]TCTGCCCACCTTGGC	2186
rs537695667	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67871007	CGATCTCCTGACCTC[A/G]TGATCCGCCCGCCTC	2186
rs537730340	snp	G/T	1.90387e-05	0.00308529	intron-variant	BPTF	GRCh38.p7	17:67913234	AGAAAATTTTAAAAA[G/T]AATTATCTCACAAGA	2186
rs537744897	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67827608	AGGAAAAAAGACCTT[C/T]TTTTTCGTTGAAGTA	2186
rs537746190	snp	A/G	0.0876345	0.190099	intron-variant	BPTF	GRCh38.p7	17:67843210	TACATACATGTAGAT[A/G]TATGTAGATATATAC	2186
rs537751440	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67968839	TATACAAAATTAGCC[C/T]GGCGTGGTGGCACAT	2186
rs537752674	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67963139	GATGTGAGTGACTTT[A/T]TGTTTCCACATGTGA	2186
rs537772004	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67877764	GCTGAGACTACAGGT[A/G]TGCACCACCATGCCC	2186
rs537774246	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67936208	ATAGCAGGGTTTTTT[G/T]TTGTTGTTGTTTTGT	2186
rs537789720	snp	A/G			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67887705	GTAGTTGGGAAGTCC[A/G]AGCCATCATCAGGTA	2186
rs537790743	snp	C/T	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67905167	GTAATCCCAGCACTG[C/T]GGGAGGCTGAGGCAG	2186
rs537799079	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67906557	GACCACATATGCACA[A/G]AGTGATAGAACGCTG	2186
rs537814417	snp	C/T	0.00358779	0.0422022	intron-variant	BPTF	GRCh38.p7	17:67890683	GTGAGGGAAGTATCT[C/T]CCCAAAGGAAAGAAG	2186
rs537850914	snp	A/T	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67883704	CCCCTGGGTTCAAGC[A/T]GTTCTTCTGCCTCAG	2186
rs537860232	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67913705	ATGAATAGGTAGTCT[C/T]TAAGATTCCTTAGAA	2186
rs537877083	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67842341	ATGACTCAATTTCCT[C/T]GACCAGTTACTCCTC	2186
rs537878280	snp	G/T	0.00358779	0.0422022	intron-variant	BPTF	GRCh38.p7	17:67956694	AACGGTCAGGCACAG[G/T]GGCTTACGCCTGTAA	2186
rs537881701	snp	C/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67835462	ATCCTGCACAGCTTG[C/G]GTAGCCCCAGCACTC	2186
rs537902739	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67951707	TTAATGTATGTATTC[A/G]TATATAAACCTGTTT	2186
rs537955229	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67848441	GCTGTCATGGAGGAC[C/T]GTACAAAGTGTCAGA	2186
rs537960535	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67863856	AAACTTACTGTGAGT[C/T]ATTAACCTTCTACTT	2186
rs537997568	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67918595	AAACCATATTATAAA[C/T]ACTGGAGTCCTAATG	2186
rs538005029	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67828281	AAATCACATGTTGGT[C/T]TTCTTTGCACCCAGA	2186
rs538102911	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67961389	TCGTAATCTCTTGTC[C/G]CAAACTAGGCTGGTT	2186
rs538114391	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67920840	AGTTCATTGTAGTAT[C/T]CAGATTGAAAATATA	2186
rs538161015	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67886464	GGGGGTGGAATTTAG[A/T]TGTTCTTTTCCTTTA	2186
rs538170842	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67861690	AAAACCTTTTAATTA[C/T]AATTACTTCCATTTG	2186
rs538211787	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67844468	TAGCCAGTATGGTCT[C/T]GATCTCCTGACCTCG	2186
rs538268771	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67897264	GAGAATCGCTTGAAC[C/T]CGGGAGGCGGAGGTT	2186
rs538292298	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67851679	GTTGTGGGCAAACAG[A/G]TGTGCAGGCTGTTCA	2186
rs538298622	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67950689	CTAAAAATACAAAAA[A/T]ATTAGTCAGGCATGG	2186
rs538305576	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67925841	TTACATCAAAGTTTG[A/G]GATGATAGCACTTTT	2186
rs538308496	in-del	-/A	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67913262	GAATATCTCATTTTT[-/A]AAAAAATGAGATAAT	2186
rs538334278	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67833014	ATGTTGGCCAGGCCG[A/G]TCTCGAACTCCTGAT	2186
rs538341209	snp	C/T	2.00114e-05	0.00316312	intron-variant	BPTF	GRCh38.p7	17:67893353	AAATAATGCAGTCTT[C/T]TTATTTTTTTGGTCA	2186
rs538349843	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67900550	GCCTGGGCAACATAG[A/G]GAGACCCTGTCTCTA	2186
rs538357474	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67857558	TGCAGCCTCGACCTC[C/T]TGGGCTCAAGCAGTC	2186
rs538362722	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67941281	CATGGTGAAATTCCA[C/T]CTCTGCTAAAAGTAC	2186
rs538365630	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67916253	GCAGCAACTTTTTGG[C/G]TAGAGCTTTCTCTTT	2186
rs538372161	snp	C/T	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67952542	TGCTGGGATTCCAGG[C/T]GTGAGCCACCACGCC	2186
rs538387023	snp	C/G	1.6516e-05	0.00287362	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911920	TCCACTGGAAACTGT[C/G]AGGACAGGCTGCCGG	2186
rs538419244	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67961866	GTAATCCCAGCTACT[C/T]GGGAGGCCGAGTCAG	2186
rs538420237	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67918121	TTGTATTTTTAATAG[A/C]GATGGGGTTTTGCCA	2186
rs538430781	snp	G/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67864193	ACAAATAATTTTGAT[G/T]ATATAAACTGTATAT	2186
rs538493889	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67857218	TGGAGTGCGAGTGCA[A/G]TGGCGTGATCTCGGC	2186
rs538499574	snp	G/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67952893	TTTTGATAAAATAAT[G/T]TGTTTTTTAATAAAG	2186
rs538529184	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67896770	TTCATGAAAGTACTA[A/C]ATACATTGAAATTTG	2186
rs538541149	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	BPTF	GRCh38.p7	17:67889653	TCTCTACTAAAAATA[C/T]AAAAATTAGCTGGGC	2186
rs538551634	snp	A/G	0.00438332	0.0466095	intron-variant	BPTF	GRCh38.p7	17:67964729	TTCTTGGCCGGGCAT[A/G]GTGGCTCATGCCTGT	2186
rs538551867	in-del	-/T	0.34437	0.231505	intron-variant	BPTF	GRCh38.p7	17:67862814	GAAAAAAATCCTTGC[-/T]TTTTTTTTTTTTTTT	2186
rs538552606	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67860066	TTAAAAGCTATGGTC[A/G]TCATTCAAATTGCCT	2186
rs538586142	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67899828	GCCACCGCGCCCGGC[C/T]TATGCTGAGTTTTCA	2186
rs538604471	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67851113	AGAGTCGGCCACTTA[C/T]CTGTGCACAGACAAG	2186
rs538608640	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67951754	AACGAGGAAGAAAAG[G/T]TATACTTTGAGAAAG	2186
rs538609213	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67974757	GCTGTGGGGAGGGGT[A/G]TGGAGTCTCCCATGC	2186
rs538645891	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67942289	CACTGCACTCCAACC[G/T]AGGCAACAGACTCCG	2186
rs538650751	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67877935	TACTGCACCCAGCAA[A/C]TTTAAAAAATTGAAA	2186
rs538659441	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67907139	GCAGTGAGCTGAGAT[C/G]AACCCACTGTGCTCC	2186
rs538660528	snp	A/C	0.00755907	0.0610114	intron-variant	BPTF	GRCh38.p7	17:67880487	TTTTAAATGCATGAC[A/C]AGAACACAACCACAA	2186
rs538663801	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67843832	ATGCAATGGCGCAAT[C/T]GTGGCTCACTGCAAC	2186
rs538666932	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67849118	TGCTTGGTAAGGGGA[A/G]TATCCATTTTCTTTA	2186
rs538669878	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67957949	GTTCCTAGGGTAATA[A/G]GGTTTGCTTTGATCA	2186
rs538679564	snp	A/G	3.29979e-05	0.00406175	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67920133	CATTGGAGTTCCAGA[A/G]ACACCAAAAGGTAAG	2186
rs538691444	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67943929	CAGATAACTGGCTGA[C/T]CATTGGGGGAGCTTG	2186
rs538716284	in-del	-/T	0.427271	0.176281	intron-variant	BPTF	GRCh38.p7	17:67879137	GTTGTTAATTATTTC[-/T]TTTTTTTTTTTTTTT	2186
rs538737722	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67968507	AATAAGGTCAGGTGC[A/G]GTGGCTCACGCCTGT	2186
rs538740588	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67838475	TGTGTAAACATGTGT[A/G]TGTACATACTTTTTT	2186
rs538759488	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67943185	TGGTGACCACAGTGG[C/T]GGTTTTATAGATGTT	2186
rs538792923	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67926474	TGACTATAGGCGCCC[A/G]CCACCACGCCTGGCT	2186
rs538813699	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67897308	ATCATGCCATTGCAC[C/T]CCAGCCTAGGCAACA	2186
rs538847964	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67921033	ACAATGTAGTGAAAC[A/C]CTATCCCTACAAAAC	2186
rs538862924	snp	A/C	1.65924e-05	0.00288027	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912811	CCCTCCACAGGCGGC[A/C]GTGTGGACATCATCT	2186
rs538881236	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67905078	TGTTTTTTAGAAGAC[A/G]CCTCAGCCGCCTGAT	2186
rs538882578	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67878439	TCATGGAGCTGGTTT[A/T]TGCTCATCTTTGGTA	2186
rs538905004	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67955763	ATCCTGAAGGCAGAG[A/T]TTGCAGTGAGCCGAG	2186
rs538906521	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67941474	ACCAAAAAACTTAGT[A/G]TATAATACTTCACTA	2186
rs538920476	snp	C/G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67957783	ATCACTTGAGCCTGG[C/G/T]AGGTCAAGGCTACAG	2186
rs538962741	snp	A/G	0.00398564	0.0444627	intron-variant	BPTF	GRCh38.p7	17:67847872	TTGTTACATTTGACA[A/G]CTAAGTTTCATAATT	2186
rs538968567	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67940781	GAAATGGTTGCTTCC[C/T]GGAGTCAAGCAGAAA	2186
rs538976960	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	BPTF	GRCh38.p7	17:67982406	ACTTGACCTAAACTT[C/T]GTTTTTATTGGTCAT	2186
rs538988055	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67924951	ATAGGGCTTCGCCGT[C/G]TTCCCCAGGCTGGTC	2186
rs539002621	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67892484	CTGTGGATAGGACAG[C/T]ATGGCATCCCAGCTC	2186
rs539029415	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67885392	AGTTCGAGCCCAGCC[C/T]GGCCAACATGGTGAA	2186
rs539066031	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67891735	CCTTTTTTTATCTGT[G/T]TACTTTGTGGATCTT	2186
rs539109781	snp	A/G	0.000115832	0.00760937	intron-variant	BPTF	GRCh38.p7	17:67920161	AAGAAATAGAATTCT[A/G]TTCTTTCATGATTAA	2186
rs539110519	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67966349	TTCTAAGCTTGTGCT[C/G]CATTCCCAACACAAA	2186
rs539165033	snp	A/G	0.0023933	0.0345097	intron-variant	BPTF	GRCh38.p7	17:67961909	AACCCGGGAGACTGA[A/G]GTTGCAGTGAGCCGA	2186
rs539177833	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67905890	GGAACATCACACACC[A/G]GGGCCTGTCGTGGGG	2186
rs539194121	snp	A/T	0.00199481	0.0315187	intron-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67919215	TAATAATAATAATAA[A/T]AATAAAATATAATGC	2186
rs539200339	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67956348	AAAAAGACAGGGTCT[C/T]ACTTTGTCACCTATG	2186
rs539207872	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67979766	ATTACCCTGGCCGGG[C/T]GCAGTGGCTCATGCC	2186
rs539254572	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67849413	CTCAAACATGATAAT[A/G]CCAGTCACTTGTCGA	2186
rs539278520	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	BPTF	GRCh38.p7	17:67889611	TCAGGGGTTCAAGAC[C/T]AGCCTGACCAACATG	2186
rs539304136	in-del	-/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67832526	CAATATTTATGAAAA[-/T]TTCAGTTTTTAAAAG	2186
rs539312217	snp	A/C	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67897753	TAAGGTATTTCTTAA[A/C]TTTCGAGAACCAGAT	2186
rs539326360	snp	G/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67925060	ATCCAGGTTTTTTTT[G/T]TTTTTTTTTTTTTAA	2186
rs539334432	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67890841	TCATATAGTAAATTA[G/T]CTGTCTTTTCATTTG	2186
rs539388004	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67961451	AATTCAAGTCCTGAA[C/T]ATCCTTCCAGAACAC	2186
rs539404840	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67903276	TATTCTTTGGTCTTC[A/G]TTTTTTGGAAGGAAA	2186
rs539406373	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67964804	AGGAGATCAGACCAT[C/T]CTGGCTAACACGGTG	2186
rs539407523	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67967775	AGTGAGCTGAGATCA[C/T]GCCACTGCATTCCAG	2186
rs539422407	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67975581	ATTTATATTTTAGAA[C/G]CTCAATCAGAAACAA	2186
rs539422885	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67861921	CCCTGAACCCCTTTT[G/T]CTCTTGCATCGTGAA	2186
rs539425143	in-del	-/A			intron-variant	BPTF	GRCh38.p7	17:67970236	GTGAAACTCCATCTC[-/A]AAAAAAAAAAAAAAA	2186
rs539428594	snp	C/T	0.0333695	0.124785	intron-variant	BPTF	GRCh38.p7	17:67925719	ACTATTTAAAAATCA[C/T]ATATAAACCAAATTA	2186
rs539471111	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67967392	TGATCCGCTCCCCCT[C/T]GGCCTCCCCAAAGTG	2186
rs539478191	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67883567	TTTTATTGGTTTTTG[A/G]TTATTCTTGAATGTT	2186
rs539480640	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67846475	CCTGTATGGTAGCCA[C/T]GAGACACATGGCTAT	2186
rs539483758	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67862381	CTACTCTAAACACTT[C/T]ATATATTTTAATTAA	2186
rs539486786	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67960671	CACCATACTTTTTAC[A/G]GGACCAAAAAGTCTG	2186
rs539522831	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67835305	ATAGCCACATGTATT[A/G]CACCACACAAATGTA	2186
rs539539473	snp	C/T	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67896213	GTGATCCGCCCGCCT[C/T]GGCCTCCCAAAGTGC	2186
rs539539999	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67876712	TTGGGTGGCTGAGGC[A/G]GGAGGATCACTTGAA	2186
rs539556817	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67853296	GTCTGTTGTCTGTTT[C/T]CTAGGTAAGCCACTT	2186
rs539557611	snp	A/T	0.0023933	0.0345097	intron-variant	BPTF	GRCh38.p7	17:67860971	CACATATTAACTTAC[A/T]GACTTCCCGTGCCTG	2186
rs539577775	in-del	-/A	0.336474	0.234568	intron-variant	BPTF	GRCh38.p7	17:67956663	AATTCAGTTCTACTT[-/A]AAAAAAAAAAAAAAA	2186
rs539600268	snp	C/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67840955	ATATTTTCTCCCTGT[C/G]AGTGCCTTGCGTTTC	2186
rs539603634	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	BPTF	GRCh38.p7	17:67824745	TGAGGTGATCGAAGT[C/T]CTAGCTGGGGCACTG	2186
rs539607353	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67966070	AAAAAAGTGGGGGGA[A/T]ATAAAAGGATATAGT	2186
rs539627732	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67973576	GCAGTGGTGCGATCT[G/T]GGCTCACTGCAGCCT	2186
rs539634895	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67979249	ACATTTTCGTAGTAA[C/T]GTAAATAATGACATT	2186
rs539664084	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67834386	TGAAAAGAATTTTGT[A/G]TTCTGCTCTTGTTGA	2186
rs539689391	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67860009	TGGAACAGTAAAATA[C/T]TTATGTTTGTCAATA	2186
rs539693862	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67867992	GCAATATCTACATAA[A/G]TTATTTGGAATTTTT	2186
rs539701374	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67937859	GTGGCTCATGCCTGT[A/G]ATCCCAGCCCTTAGG	2186
rs539704896	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67881543	GTCTCGCTCTGTCAC[C/T]CAGGCTGGAGTGCAG	2186
rs539723158	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67873577	CGAAACTATTTTACT[C/G]TGTGTACTAGGAATG	2186
rs539733830	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67973232	ACAAAAAATTAGCAA[A/G]GCATGGTGGCAGATG	2186
rs539740621	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67828754	GCTGGTCTTGAACTC[C/G]CGACCTCAGTTGATC	2186
rs539744942	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67966503	TTCATTGATGTAGTA[A/C]CTCAACCAGGAAACT	2186
rs539753402	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67882359	ACATATTTTTGAAAA[A/G]AAAAAGATCATCAGT	2186
rs539763942	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67905137	CCAGGCAGCCAGGCG[C/T]GGTGGTTCACGCCTG	2186
rs539784194	snp	A/G/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67914734	TAGGCACTGGTCCCA[A/G/T]TCAAGTGTTGCTCGG	2186
rs539853883	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67904305	AAAGTGCTGGAATTA[C/T]AGGCATGAGCCACTG	2186
rs539855426	snp	C/T	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67854987	CATTGTTTTTTGATG[C/T]CTAGGCTAGGAAATA	2186
rs539861502	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67953823	GACCTCAGGTTATCC[A/G]CCCACCTCAGCCTCC	2186
rs539888595	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67841301	GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG	2186
rs539893391	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67947986	TTCCAGTCACAGAAA[A/G]TTTTTGTCTCATCTG	2186
rs539939387	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67843136	GATATATACCTATAT[C/G]TACATACATATAAAT	2186
rs539939432	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67890363	TTCTTTGTGATGGGC[C/T]TATTGTTTGCTGTTA	2186
rs539998130	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67884264	GCATGCACCACCACA[C/T]CTGGATAATTTTTGC	2186
rs540002394	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67897009	AGGGGGAGGAAATAA[C/T]ACAGCACAAATAACC	2186
rs540058342	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67918168	GTCGAACTCCTGACC[C/T]CAGGTGATCTGCCCA	2186
rs540082642	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67873468	CATCTCAAAAAAAAA[A/G]AAAAAGAAAAAGAAA	2186
rs540091696	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67966986	ATGCCTGTATTCCCA[C/G]CTACTCAGGAGGCTG	2186
rs540104445	snp	A/G	9.91883e-05	0.00704161	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67909710	GATGCTGCAAAAGGA[A/G]CAGACCAAAATGAAA	2186
rs540126651	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67960036	TATTCTTACCATTGA[C/T]GCTAGTAAAGTAAAA	2186
rs540165759	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67876092	CTGACCTTTCCAGTT[C/G]TGTAGATACTAACAA	2186
rs540176451	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67917057	AACGTTTAGTACCTC[C/G]ACACACAATGTTTAG	2186
rs540191989	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67979321	GGAAGGCCAAGGCAC[A/G]TGGATCATCTGAGAT	2186
rs540224149	in-del	-/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67863172	GGTTTTTCTGGAGAC[-/T]TTCAAAGAGAATCTG	2186
rs540254236	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	BPTF	GRCh38.p7	17:67889131	GAGGCTGATGTAGAT[C/T]TGTAGCCTGCTGCCA	2186
rs540263057	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67905722	TCTTAAAAAAAAAAA[-/T]CTTAATTCAGTACTA	2186
rs540267671	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67943044	CTTATATATACCTAA[C/G]ATACATACCGAAGTA	2186
rs540276639	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67955190	GGCTGAGGCAAGAGA[A/G]TGGCATGAACCCGGG	2186
rs540310087	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67897372	AAAAAAAAAAAAAAA[A/G]TAAAGAAAGAGACAT	2186
rs540335519	snp	A/C	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67924490	GATTTCACTCTTATT[A/C]GATGCCAGATGCCTA	2186
rs540364816	snp	A/G	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67972700	TCCTCCATAATATAT[A/G]CTCACCTATGTGTTC	2186
rs540372602	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67839701	ATCCATTCAATAGTT[G/T]GATATTTCAGTTATC	2186
rs540404919	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67853765	AAAACTTTGCATTTA[G/T]ATTTTCTATAGATTT	2186
rs540416771	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67861243	TTCTCTCCATTCCCA[C/G]TGTCCCTCCGTGATA	2186
rs540418268	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67925091	GTGTATCTCACGTCT[A/G]TCTTATTGTCATTAT	2186
rs540458854	snp	C/T	0	0	intron-variant	BPTF	GRCh38.p7	17:67973499	GGCAGTTGCCCCAAA[C/T]CCTTTTTTTGTTTTT	2186
rs540462930	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67884671	TCTGCCTGCCTCAAC[C/T]TCCCAAATTGCTGGG	2186
rs540476795	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67859385	TCCTGGGTTCAGGCA[A/G]TCCTTTCACTTCAGC	2186
rs540508533	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67845953	AAGAGGTATATGAAA[A/G]CTATTTTTATCTTTC	2186
rs540533448	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67910370	CTTCTCTTGGCGATA[C/T]ACCTAGGAATGGAAT	2186
rs540533626	snp	A/G	3.33267e-05	0.00408194	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67826209	ATTCTGAGGACGACG[A/G]GGAGGATGAGATGGA	2186
rs540541645	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67961589	CCGTGGCTCATACCT[A/G]TAATCTCAGCACTTT	2186
rs540546040	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67851143	GGAGAGGTCTCATGA[A/G]GCTTCGGCAGAGTCT	2186
rs540555730	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67896103	GAGTAACTGGGACTA[C/T]AGGCACCCACCACTA	2186
rs540584520	snp	A/C	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67840418	GGCCAAGATACCAAA[A/C]TCTTTATTTAAGATG	2186
rs540606556	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67832675	CCAGCACGTTTTTAT[A/G]CCCCCGCAAAAGAAG	2186
rs540620509	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	BPTF	GRCh38.p7	17:67824072	CTGCCCTGGTGATCC[A/G]CCCTCCTCAGCCTCC	2186
rs540625155	snp	C/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67939222	ACAACAAAAAGGTGT[C/G]GGGGAAGTATTCTGA	2186
rs540644206	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67896232	CTCCCAAAGTGCTGG[A/G]ATTACAGGCATGAGT	2186
rs540657172	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67833341	GCCTCAGCCTTCCAG[C/T]CTCCAGAGTAGCTAG	2186
rs540657755	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67965113	TGGGGAGGCTGAGGC[A/G]GGTGGATCACAAGGT	2186
rs540662825	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67866825	GGGGATACATTCTGA[A/G]AAATGTGTCATTTGA	2186
rs540685366	snp	A/G	0.00279162	0.0372561	intron-variant	BPTF	GRCh38.p7	17:67892146	TAGACCTATTTTTGA[A/G]TTATATTTTCTCTGT	2186
rs540706157	snp	A/T	0.0023933	0.0345097	intron-variant	BPTF	GRCh38.p7	17:67971389	TGGCCCATTTTAGGC[A/T]TTTTTTTAAAAACAA	2186
rs540713260	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67831539	TTGTATTGAAACATG[C/T]GTATCACAGGACTGG	2186
rs540720797	snp	A/C	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67826563	GCAGTTTGCAGGCCA[A/C]ACTCGCTCGCTCTCT	2186
rs540722910	snp	G/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67846701	ATAGCTTAGGACTTG[G/T]GTGGGTTTGTTTGTT	2186
rs540733507	in-del	-/ATTAAAACAA	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67939711	TGAAACCCCATCTCT[-/ATTAAAACAA]ATACAAAAAATTAGT	2186
rs540781381	in-del	-/C			intron-variant	BPTF	GRCh38.p7	17:67903103	ATATGGGCCGACCTT[-/C]CCTCATCCTTCCTCT	2186
rs540811692	in-del	-/A			intron-variant	BPTF	GRCh38.p7	17:67976082	ATCTTTAAAAAAAAA[-/A]TAAATAAATCAAGAC	2186
rs540852495	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67830705	AGTCTCAAGTAACTC[A/G]GTTTAGCAAGAGCCT	2186
rs540883923	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67938636	TTGGGGGGAAAATAG[A/G]CTTCCGTGTTACAAC	2186
rs540889033	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67894984	ATTACAAAACTAAGG[C/T]TATGGTAAATAATAG	2186
rs540890151	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67947050	TCCCATTCACAGTCC[A/G]TGAAACTCACTTATC	2186
rs540933884	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67958736	TTGGGAGGCCGAGGC[A/G]GGTGGATCACCTGAG	2186
rs540966461	snp	A/G	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67977801	GTGAGCCGAGAAGGC[A/G]CCACTGCACTCCAGC	2186
rs541025393	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67957128	TCTCTACTAAAAATA[A/C]AAAAATTAGCCGGGC	2186
rs541088691	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67873086	ACTCTGTCTCTAAAA[A/T]AGTAAAAAATAAATT	2186
rs541100520	snp	C/T	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67909124	ACAGGCATGAGCCAC[C/T]GCACCAGCCTATAGT	2186
rs541145093	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67943457	GACAGAAGAGAGAGC[A/G]CCTAGAGAATTTTAA	2186
rs541161527	snp	C/T	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67916730	AAGATTGCTCCACTG[C/T]ACTCCAGCCTGGGTG	2186
rs541177353	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67907977	AACTTCAAGGAGTCC[A/C]AGAACCATTGAAATA	2186
rs541182534	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67977075	TTTAGTGCTAGAAGA[G/T]TATGGAAGAATAAAT	2186
rs541188138	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	BPTF	GRCh38.p7	17:67984697	GCAATGATGCCATCT[C/T]GGCTCACCACAACCT	2186
rs541214450	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67940227	TACAGACAGCAGAGA[A/C]TGGATAACGGTTGGC	2186
rs541219259	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67962763	AATTACTCTATGTAC[A/T]TTCTTAGTTTTCTTC	2186
rs541231256	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67888229	TTCAAAAACCTCTTT[C/T]CCACAGTTACATCCT	2186
rs541231605	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67964867	AGCTGGGCGTGGTGG[C/T]GGGCGCCTGTAGTCC	2186
rs541237635	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67958793	AACATGGCGAAACCC[C/T]GTTTCTACTAAAAAT	2186
rs541251457	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime	BPTF	GRCh38.p7	17:67984088	TCCTTTTACTTTTTT[A/T]AAAAATGTTACATAT	2186
rs541256388	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67872121	GTGAGCCACTGCGCC[C/T]AGCCCTGTTTTTGGT	2186
rs541300619	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67915263	CTTCATTTTCACATT[G/T]AACTGATAGTTGTCC	2186
rs541339581	in-del	-/TC	0.0142736	0.0832652	intron-variant	BPTF	GRCh38.p7	17:67879663	AGCATGGTACTGACA[-/TC]TGCATCTGGTGAGGG	2186
rs541366983	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67948011	CATCTGTAGAGGCAT[A/G]GAAGAATGATGTCTT	2186
rs541377555	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67887500	AGGAGGGTTATCCCC[A/C]TCCCAAGAATATATA	2186
rs541392753	snp	C/T	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67851351	ACAGTGCTGGATGAA[C/T]GCCTCAAGGGGCTCA	2186
rs541397728	in-del	-/A	0.0310569	0.120681	intron-variant	BPTF	GRCh38.p7	17:67835213	GAGAACCCATCTCTT[-/A]AAAAAAAAATTTAAG	2186
rs541415954	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67858390	TTTGTCAGCAAGGTC[A/G]TTCCAAATGGTGAAA	2186
rs541446168	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67860464	ATATGTTATTTGTAT[A/G]GATTAGTGAAGCTTA	2186
rs541460121	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67958205	TGGTGGCACGTGCCT[A/G]TGGTCCTAGCTAGGT	2186
rs541489186	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67966211	CTGCTACCTCATCAT[G/T]AACCAGCTGTGGTAA	2186
rs541520680	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	BPTF	GRCh38.p7	17:67983544	TTGGTTTGTTTGTTT[C/T]TTCCACGTAAGGAAA	2186
rs541520750	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	BPTF	GRCh38.p7	17:67825040	GGTGCCCTCGGTCGC[C/T]TGGGCCGCCCCTCTC	2186
rs541539287	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67842498	CTCTCCTCTAAACTC[C/G]AGTTATGTATTTCCA	2186
rs541553135	snp	A/C	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67857728	CTTCTCGGCCTCTCA[A/C]AGTGCTGGGATTATA	2186
rs541556869	in-del	-/AT			intron-variant	BPTF	GRCh38.p7	17:67925691	TACAGTATTATTAAC[-/AT]AGTTATACATAACTA	2186
rs541590152	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67829688	CGAATAACACATAAA[A/G]AAGTATGATTGATGA	2186
rs541603724	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67909975	CATCAATCTTAGAAC[A/G]TTTTCATAACCTTGA	2186
rs541607500	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67921505	CATTCTAGCATGGGC[A/G]ACAGAGTGAGACTCC	2186
rs541610241	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67964608	CGTCAGCTTATCTCA[C/T]ACTCACAAGAGTGTT	2186
rs541614905	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67930874	GGACGAGAATTGCTC[A/G]AACCCACAAGGCAGA	2186
rs541678404	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67969096	GGCTTGAGCCCAGGA[A/G]TTCAAGACCAGCCTG	2186
rs541685381	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67923574	TGCAACCTCTGCCTC[C/G]TGGGCTCAAGCAATT	2186
rs541699268	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67873161	TGGATATACATGGTA[G/T]TAAGTGTTTCTTATG	2186
rs541732146	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67888310	TCAGTAGATCTGGGC[C/T]GGGCTCGGTGGCTCA	2186
rs541735572	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67829352	TTTTTTTTTCCTTAT[C/G]TCTTCTAAAAAAAAA	2186
rs541746925	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67923155	CTGCCTCCCAGGCTC[A/G]AGTGATCCTCCCACC	2186
rs541748893	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67931384	AGGCTGAGGCAGGAG[G/T]ATTGCTTAAGCCCAG	2186
rs541754024	snp	C/T	0.00914312	0.0669923	intron-variant	BPTF	GRCh38.p7	17:67964775	GGAGGCCAAGGTGGG[C/T]GGATCACAAGGTCAG	2186
rs541762651	snp	A/C	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67839137	TGGGTAATAAAAAAA[A/C]AAGAAAAAAAAGAAA	2186
rs541805949	snp	C/T	0.00557542	0.0525036	intron-variant	BPTF	GRCh38.p7	17:67967805	GCCTGGACGACAGAG[C/T]GAGACTCTGTCAAAA	2186
rs541836745	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67900975	AGTGAGCTATGATTG[C/T]GCCACTGTACTGCAT	2186
rs541842783	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67943728	ATATTTTCTCTGCCT[A/G]CCCCATAAAGTCACA	2186
rs541862155	in-del	-/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67966454	ACTTAATATAAAATA[-/T]TTTCATGTATCAAAT	2186
rs541875488	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67844527	GCTGGGATTACAGGC[A/G]TGAGCCACCACGCCC	2186
rs541884406	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67910642	CTGTCTCTACTGAAA[A/G]TTCAAAAATAAGCCA	2186
rs541908427	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67895661	AGACACGGGGTCTCA[C/T]TATGTTGCCCAGGCT	2186
rs541909083	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67874341	CCTCTGTTTTCTCTT[C/T]TTACAGTTGAGGAAA	2186
rs541910039	snp	A/C/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67937639	GAGGCAGGAGTGGAC[A/C/G]TGGTGACATTGAAGG	2186
rs541927509	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67902905	CTAGCGCTCTTAGAG[A/G]CAAGAGCTCCTTTCT	2186
rs541936740	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67847166	GTTGATCTGAGGATA[A/G]AAATAAGATAATGCA	2186
rs541940284	snp	A/C/G	0.000798403	0.0199641	downstream-variant-500B	BPTF	GRCh38.p7	17:67984795	CACCACGCCTGGCTA[A/C/G]TTTTGTATTTTTAGT	2186
rs541981478	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67945181	GCTTGGACCATAGCC[A/G]TGCTCCACTATGCTC	2186
rs542001088	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67978341	TCTCACTCTGTTGCC[C/T]AGGCTGGAGTTCAGT	2186
rs542007106	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67881832	TTGGAGACTGTAATA[C/T]GGAGTTTTGGGGATT	2186
rs542022662	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67938873	TGGGCAGTGTGTGGA[C/G]AGTGAATTCACAAAT	2186
rs542030601	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67964931	ATGAACCCGGGAGGC[A/G]GAGCTTGCAGTGAGC	2186
rs542037857	in-del	-/G	0.0023933	0.0345097	intron-variant	BPTF	GRCh38.p7	17:67882045	TCGCCATGTTGGCCA[-/G]GCTGGTCTCGAACTC	2186
rs542043995	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67873825	AGTAACACCCCAATA[A/G]TAACAAACACACCAA	2186
rs542070501	snp	C/T	0.00358779	0.0422022	intron-variant	BPTF	GRCh38.p7	17:67916881	TAGCCTTTGTCTACA[C/T]CATAATCAACCACTA	2186
rs542082094	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67872317	TGGTCTAAACTTAGT[A/G]GGCAACTAAAACAAT	2186
rs542113566	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67930804	CAAAAAATTAGCTGG[A/G]CATGGTGGCATGTGC	2186
rs542136314	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67971857	AAAGAGAAGAAAAAA[A/C]TTACACGTTAGCAAA	2186
rs542175328	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67976292	AGACTGGCCAACATG[A/G]GGAAACCCCGTCTCT	2186
rs542181412	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67880894	TTTTGTGGCCCAACA[C/T]TTAATTAATGTTGAT	2186
rs542192985	snp	G/T	1.72323e-05	0.00293528	intron-variant	BPTF	GRCh38.p7	17:67944420	GTTACTACTACACGT[G/T]GCTGGGCTAACAGAG	2186
rs542196684	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67916161	GACCTGCTCTGTCCA[A/G]GTCAGAGGATTCATA	2186
rs542225566	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67844565	TTTTTTTTTCTTTTT[C/T]TTTTTTTGTATTTTT	2186
rs542229603	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67953289	TGAGACGGAGTCTTA[C/T]TCTGTCACCCAGGCT	2186
rs542232083	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67975690	TGCACAGTAAACATA[C/T]ATACTTGTTAGAACT	2186
rs542236145	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	BPTF	GRCh38.p7	17:67983375	CATACTAACGAGAAC[A/G]GTAATGCGACAAGAT	2186
rs542263368	in-del	-/AGC	8.33604e-05	0.00645548	cds-indel, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67875690	TCAGAAACCCCCGAT[-/AGC]AGCAACATGGCAGAG	2186
rs542267002	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67857895	CAGGTTCAAGCGATT[A/C]TCCTGCCTCAGCCTC	2186
rs542282351	snp	A/G	1.66743e-05	0.00288736	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67893664	ACTCTGAGACTGACT[A/G]TCACCCAATTAGAAA	2186
rs542322777	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67936974	ACAATTATTCAGTAC[A/T]ACCTATGTGCCAGAT	2186
rs542328495	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67860382	ATGCAGAGGTTTTAA[C/T]TGTAATGTTACCAAT	2186
rs542357232	snp	A/G	6.59359e-05	0.00574139	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67866598	TTCTAGAAGAAATGC[A/G]TGAAGAAATCCACCG	2186
rs542358722	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67852274	TTTTATAGATACCTG[C/T]CCAATTTTTTCTTTT	2186
rs542360002	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67843993	TGGTCTCAAACTCCT[G/T]ACCTCAGGTGATCCA	2186
rs542380462	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67830704	CAGTCTCAAGTAACT[C/T]GGTTTAGCAAGAGCC	2186
rs542400432	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67857779	GACTAACAATATTTC[C/T]TTCTTTTTTTTTTTT	2186
rs542401762	snp	C/T			intron-variant, utr-variant-3-prime	BPTF	GRCh38.p7	17:67982053	TTTTCCAGTGAGCTA[C/T]TATGTTTAGTGTACA	2186
rs542415553	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67958244	GGCTGAGGTGGGAGG[A/T]TCACTTGAGCCTGGG	2186
rs542426310	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67860855	CGTGGACCACCACAC[A/G]CCTTTAAACAGCATT	2186
rs542446513	snp	C/G	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67922412	GATAGGGAAACACAT[C/G]TTGTACACCCAAGTG	2186
rs542469306	snp	A/G	0.0232847	0.105357	intron-variant	BPTF	GRCh38.p7	17:67856922	AGCTTGAAGGGGAGA[A/G]TGGTGGTTTAGGAAT	2186
rs542511071	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67943237	TACTTGGTGTTTTGT[A/G]CATTTTGTGCATAAA	2186
rs542530803	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67849834	TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG	2186
rs542530824	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67857254	GCAAGCTCCGCCTCC[C/T]GGGTTCACACCATTC	2186
rs542550059	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67958693	CTGAGATTGTGCCAC[C/T]GCACTCCAGCCTAGG	2186
rs542586405	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67963784	AATGAGATTAAAATA[C/G]CCTGACTTGTTTGGA	2186
rs542615625	in-del	-/G	0.0155061	0.0866753	intron-variant	BPTF	GRCh38.p7	17:67931035	CTTTGGGAAGCCAAG[-/G]GGGGGCGGATCACAA	2186
rs542616396	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67829393	GTGCAGAACGTGCAG[A/G]TTTGTTGCATAGGTA	2186
rs542633148	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67927910	TTTTTTTTAGAGATG[A/G]AGTCACTCTGTCACC	2186
rs542633990	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67833836	GCCTCCCAAAGTGCT[C/G]GGATTACAGGTGTGA	2186
rs542693946	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67894816	CATCTGTTTTTAAAG[C/T]TCATTGTCCAACCAA	2186
rs542711155	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67828444	TATTTAAGATTGATG[A/G]GTGTGCATATGCTGA	2186
rs542711477	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67837217	GAATTCAGGCTCTTT[C/T]TGCGTTTACAGACAG	2186
rs542720259	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67870075	AAAGAGAACATTGAG[C/G]TTTAGGCCACAATAT	2186
rs542723511	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67964494	AGTTTCCAATCTTAG[A/G]ATGATTATTTACTGA	2186
rs542732633	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67914096	AAATCAGAATCAGTC[A/G]TAGTTGCAGTTAGAT	2186
rs542773932	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67928734	AGCAAACAAGCTGTA[A/G]CGGTTGGTTTGTTAC	2186
rs542791525	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67951024	TTTTTTGTCAGGCTG[A/G]TCTCGAACTCCTGGC	2186
rs542794541	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67899539	GTTTTTTTTCTTTTT[C/T]TTTTTTTTTTGAGAC	2186
rs542848239	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67827850	GTCTGGTGAATGAAG[A/G]GAATGAATCAAGTGT	2186
rs542857885	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67906644	TGACAGGATTACGGT[G/T]TCTTTGCACTCTCTT	2186
rs542878831	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67926560	CGATCTCCTGACCTC[A/G]TGATCCGCCTGCCTT	2186
rs542894780	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67935764	GAGGTCAAGGCAGGG[A/C]GAATTGCTTGAACCC	2186
rs542895534	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67892764	GCTTTCTGAAATACT[A/G]TTTTACTTTATGATG	2186
rs542918573	in-del	-/AT	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67935112	TCAAAAGTTAGAAAC[-/AT]ATATAAAACAAGTTT	2186
rs542923939	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67942709	TCATAAGAATCAAAA[A/G]CTAAGAACAACTCAG	2186
rs542944277	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67934696	AACCAACATGGTGAA[A/G]CCCCGCCTGTACTAA	2186
rs542949438	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67968063	TGGTAATAGGAGCCA[C/T]GAGTAATCGTATCAA	2186
rs542964702	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67970791	CCTACATCATTTTAA[A/G]TTATATGAAATTAAA	2186
rs542993060	snp	A/C/G			intron-variant	BPTF	GRCh38.p7	17:67863564	TCTAGAATTACAGGC[A/C/G]TGAGCCACCACGCCC	2186
rs542997570	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67863311	CATTTTTTTGAGACA[C/T]GGAGTCTCTGTTGCC	2186
rs543006482	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67830649	AGGGAGAGGGAGCGG[A/G]AGCGGGAGGGAGCAG	2186
rs543030392	snp	C/T	0.00279162	0.0372561	intron-variant	BPTF	GRCh38.p7	17:67842187	TACATATGCTTTCAG[C/T]GTATATCTATATGCA	2186
rs543032105	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67829055	GGGTGTCATAATCTC[C/T]AAATACTTTGGATTT	2186
rs543044671	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67968560	GAGGTGGGTGGATCA[C/T]GAGGTCAGGAGATCG	2186
rs543051171	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67929836	ATTTAAAATGCTGGG[C/T]CAGGTGCGGCGGCTC	2186
rs543075670	snp	A/C			intron-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67918969	TGAGGTCAGGAGATC[A/C]TGACCATCCTGGCTA	2186
rs543109191	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67877992	ATTAAGTGAATAACT[G/T]GATGGATGTTTACGA	2186
rs543132763	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67870650	TGAAAACAATGGAAA[C/T]TACTGGGGTTCTGAT	2186
rs543185179	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67844101	TTTTTTTTTTTTAAG[A/G]TGGAGTCTCACTCTG	2186
rs543186532	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67879919	CCTCCCATTAGGCCC[C/T]ACCTCCAACATTGGG	2186
rs543195304	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67919323	GGAGGATCACTTGAG[A/G]CCAGGAGTTTGTGAC	2186
rs543199470	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67943427	TTCAGGGTTTCTAGT[G/T]GAATTACAGTTCTGG	2186
rs543224718	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67894851	CATATAGCTCCTGAG[G/T]AGACCCAGGGCTGTG	2186
rs543229787	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67890948	CAATGGAAATTTAAC[A/G]GTGATGCAGTAGTTT	2186
rs543239449	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67956887	GAGAATGGCATGAAC[C/T]CAGGAGGCGGAGCTT	2186
rs543244837	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67877209	TAGATAAGGTCTGGG[C/T]CCTTGGTGACTTACA	2186
rs543246636	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67837923	AGTGGTGGAAAGTAC[C/T]ATGGAAATGGAGTTC	2186
rs543252757	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67952137	AACATGGTGAATCCC[C/T]GTCTCTGCTAAAGCT	2186
rs543260914	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67942839	ACAAATATATAATGG[G/T]AAGCTAAAGAAGCAA	2186
rs543265319	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67980984	GCAACATGGGGAAAC[C/G]CCATCCCTACAGAAA	2186
rs543271564	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67841632	GTCTTGAATTCCTGG[A/G]CTCAAGCAGTCCACC	2186
rs543274462	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67930797	AAAAATACAAAAAAT[C/T]AGCTGGGCATGGTGG	2186
rs543296100	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67867615	GTTTTCCTCTGGGTT[A/G]TCGGTTTCTCAGACT	2186
rs543299957	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67974848	CCGAACCCGGTCCTT[C/T]TGGGTTTTTAGGAAA	2186
rs543308176	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67842000	ATATATACCTAAACT[A/G]TCTACTTAGAGTTAG	2186
rs543313196	snp	C/T	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67936833	ATAAAGCATATAAAA[C/T]ACTATCCCCATTTTA	2186
rs543329462	snp	A/T	0.00279162	0.0372561	utr-variant-3-prime	BPTF	GRCh38.p7	17:67984015	GCTCAATATGAAAAC[A/T]TGAAAAAATTTTTGC	2186
rs543387596	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67910347	TTTTTTGTGGCCATG[C/T]GTTTTCACTTCTCTT	2186
rs543416875	snp	A/G			utr-variant-3-prime	BPTF	GRCh38.p7	17:67982407	CTTGACCTAAACTTC[A/G]TTTTTATTGGTCATA	2186
rs543440575	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67922208	GTATCCCTTTGTACA[A/G]TTCAGGTCCTGCTTT	2186
rs543496056	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67830030	AAGCTAAAGGCATAT[C/T]GCTGAATAATGCTTT	2186
rs543496130	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67965071	AGGGGACTGGGCGTG[A/G]TGGCTAACACCTGTA	2186
rs543513410	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67951193	AGCTTAACCTTCAGC[A/C]TCTCTCTCTCTCTCT	2186
rs543531087	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67907436	TCTCAGCTCACTGCA[A/G]CCTCCACCTCCCGGG	2186
rs543537530	in-del	-/G	0.030278	0.119257	intron-variant	BPTF	GRCh38.p7	17:67964795	ACAAGGTCAGGAGAT[-/G]CAGACCATCCTGGCT	2186
rs543555598	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67958151	TGGCCAACATGGTGA[A/G]ACCCCATCTCTACCA	2186
rs543574039	in-del	-/A	0.0333695	0.124785	intron-variant	BPTF	GRCh38.p7	17:67847674	GCCAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA	2186
rs543607919	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67926624	CCACCGCACCCAGCC[A/C]GTATATTACTTTAAA	2186
rs543660109	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67900026	ACATATTTTTGAAAA[G/T]TTTAATGAAGCAGAA	2186
rs543660135	snp	A/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67892932	TCCATGGGGTCTTAC[A/T]CTGTAGCTGGAATGA	2186
rs543664500	in-del	-/TT	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67881260	GATTGCTACTATCAC[-/TT]TTAAAAGTTAAAAAG	2186
rs543671958	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67918658	AGTGAATATGAATGT[A/G]TATGTGTATGTATAT	2186
rs543723663	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67936492	CACAGAGCCTTTGTT[A/G]CATAATGCCCTATGT	2186
rs543727413	snp	C/T	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67906894	GAAGAAGGTAAAGAA[C/T]AGGAAAATGCCTTTA	2186
rs543733242	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67927586	AGTTGGATAAATTAA[C/T]ATTACAGTGAAACAG	2186
rs543750666	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67963869	GGTACAAGCTCTGAG[A/G]CTCTGTTATTAGCTT	2186
rs543753654	in-del	-/A	0.00478085	0.0486577	intron-variant	BPTF	GRCh38.p7	17:67842000	ATATATACCTAAACT[-/A]TCTACTTAGAGTTAG	2186
rs543759270	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67891183	TGAGACCCTGTCTCA[A/G]AAAAAAGAAAAAAAA	2186
rs543782427	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67857287	CTGCCTCAACCTCCG[A/T]GTAGCTGGGACTACA	2186
rs543788915	snp	A/C			utr-variant-3-prime, downstream-variant-500B	BPTF	GRCh38.p7	17:67983300	TTTATCATTCCCAGT[A/C]CATTGTCATCACGTC	2186
rs543842036	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67879324	TTTTTGTATTTTTAG[A/T]AGAGACGGGGTTTCA	2186
rs543843176	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67850845	TATAAACATATTAAA[C/T]GCTCTGCATTGTTCT	2186
rs543849807	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67940973	AAGACTCGATATTGT[G/T]AGCAAGTCTTCTAAT	2186
rs543854780	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67895105	TATAGTTTTTAAAAT[A/G]TAAATACAAGCCAGG	2186
rs543872635	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67884199	CTGTAGTGCAGTGGC[A/G]CAATCTCAGCTCACT	2186
rs543894284	snp	C/T	0.000399281	0.0141238	missense, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67891898	GTGAATCTCCTGGAG[C/T]TGGAAAAGGAGCATC	2186
rs543899127	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67835814	GGGACTACAGGCACC[C/T]GCCACCATGCCCGGC	2186
rs543914126	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67899585	GCTCAGGCTGGAGTG[C/T]AGTGGTGCAATCTCA	2186
rs543954995	in-del	-/AA	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67839130	GGGAACCTGGGTAAT[-/AA]AAAAAAAAGAAAAAA	2186
rs543977673	snp	C/G/T			intron-variant	BPTF	GRCh38.p7	17:67939315	AGAAACACAAAGATA[C/G/T]ATATGTGTATCCACA	2186
rs544001860	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67920371	AGGGCTATAATAATA[C/T]CTCTTGTAATTAAGA	2186
rs544026323	snp	A/T	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67870726	AGCCTGTCTGATGAC[A/T]TTGACTTGATGTTAA	2186
rs544059054	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67855562	AGACTGAGGGTCATA[A/G]TCTGGCCTCAGTGTT	2186
rs544063618	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67869308	AAAAATATTTTCTGT[A/G]TGTTAGATTATGTAT	2186
rs544066144	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67884615	GTGATGGAGTTTCAC[C/T]GTGTTGCCCAGGCTG	2186
rs544087730	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67971278	GAATCAGGGTTTCAC[C/G]ATGTTGGCCAGGCTG	2186
rs544116626	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67968936	CATTGAGCCGAGATC[A/G]CGCCATTGCACTCCA	2186
rs544121686	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67869811	ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA	2186
rs544196591	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67842153	TTTCAATATATGTAG[A/G]TACATATAGATATGT	2186
rs544202368	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67862142	CACCACACCCGGCTA[A/C]TTTTTGTATTTTTAG	2186
rs544217211	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67972804	AAATGAAAATTAGTC[A/T]AGCAGTAAGTAACCA	2186
rs544238834	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67882091	CCGCCCACTTCAGCC[C/T]CCCAAAGTGGTAGAA	2186
rs544333371	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67848991	GTTTCTTTTGTGGGC[A/G]TACATTAATGTCTTT	2186
rs544335813	snp	C/T	3.3605e-05	0.00409895	missense, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67875703	ATAGCAGCAACATGG[C/T]AGAGAAGAAGGTGGC	2186
rs544360238	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67962072	CACATGAGCCTGGGA[C/G]GTCCAGGCTGCAGGG	2186
rs544380586	snp	C/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67862606	GAGCTTAGGACCTAG[C/G]TTTTGTCTTTAATTG	2186
rs544386111	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67833594	TTTTTTTTTTTGAGA[C/T]AGAGTCTCTTGTCGC	2186
rs544420927	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67919325	AGGATCACTTGAGGC[C/T]AGGAGTTTGTGACCA	2186
rs544422059	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67967877	AGGAGTAGCTATATC[A/C]GATGGTGTCTGAGTG	2186
rs544440922	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67946576	GAGGACTAAGATGGG[A/G]AGAATGGAGTTATGA	2186
rs544452401	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67829848	ATAGCTCACTCCTAA[C/T]ACAAGAAATAACTCA	2186
rs544453002	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67954549	CCTAATGTTAGTGTT[C/T]GGCCACCTCTTCTTC	2186
rs544473191	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67853914	TAATGTATTGATTTG[C/T]AATGATGTCACGTCT	2186
rs544512122	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67846042	ATCCTGTTTTGCTAC[C/T]GAAGCAAAATTTTTT	2186
rs544518211	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67955999	CAAAAAAGAATTCTC[C/T]GGGTGTTATGATACA	2186
rs544529409	snp	A/T	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67932434	GCCAGGCTAGGTGAC[A/T]CTCCCCTGTAATCCC	2186
rs544537903	snp	A/G	3.30737e-05	0.00406642	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912406	ACCCTGCCATCAACC[A/G]AAGAGTCTGACAGTA	2186
rs544538261	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67826655	GGGCAGGATTGAAAC[C/T]TTGGCAAACACATAT	2186
rs544585659	snp	G/T	8.40668e-05	0.00648277	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67826333	TACCTACAGCAGCAC[G/T]CCAGGTACCCACCCA	2186
rs544590660	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67939461	TGTTCTACATGGGGG[A/G]AAATTCCACTTGCCT	2186
rs544601686	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67960354	GCAGTTGTTTTTTTT[-/T]GTATTAAAATACTGC	2186
rs544603653	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67947411	TAAAATTTCAGCTGT[A/G]TTACTTACTGTTTGT	2186
rs544607702	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67924673	GACCTCCCATCAGCA[A/G]GGGGAGTTGGTGCTG	2186
rs544616614	in-del	-/A	0.0023933	0.0345097	intron-variant	BPTF	GRCh38.p7	17:67939674	CGAGGTCAGGAGATC[-/A]AGACCATCCTGACTA	2186
rs544624890	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67892119	TAGGGGCTGGAAATT[G/T]GTAGAAATTTGTAGA	2186
rs544639653	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67974997	CTGACTAGGTCTTTC[C/T]GGTGACCAGCCCCAA	2186
rs544653789	snp	A/C	0.0295035	0.117819	intron-variant	BPTF	GRCh38.p7	17:67843222	GATGTATGTAGATAT[A/C]TACCTATATATCTAC	2186
rs544665129	snp	A/G/T			intron-variant	BPTF	GRCh38.p7	17:67950613	GAGGCTGAGGCGAGC[A/G/T]GATCATTTGAGGTCA	2186
rs544681619	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67918848	GGACAGGTAAGGGGG[A/G]AGGGAGTTATTTTCT	2186
rs544687624	in-del	-/A	0.465158	0.127307	intron-variant	BPTF	GRCh38.p7	17:67930116	GCCAGACCTTGTCTC[-/A]AAAAAAAAAAAAAAA	2186
rs544700698	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67899469	TATTTTCCTGGGAAC[C/T]TTCTTTGATAGTAAC	2186
rs544705240	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67827329	CCCGAAATCCGTAAT[A/G]AATTTCTCCATGGTA	2186
rs544728021	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67883093	GGCCCAGGTGGGCGG[A/T]TCACAGATCAGGAGT	2186
rs544744948	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67925411	GCTCATGCCTGTAGT[C/T]CCAGCATTTTGGAAG	2186
rs544745949	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67884884	TGTAATTTTCCCTTC[A/G]TGTATTGTGAGACTT	2186
rs544754149	in-del	-/AAA	0.00636936	0.0560724	intron-variant	BPTF	GRCh38.p7	17:67935858	AAACTCACAAAACTG[-/AAA]AAAAGAATTTTGTAT	2186
rs544755249	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67874691	TATTTCATAGGTCTA[A/G]TGCTTTAAAAATACT	2186
rs544768410	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67896258	TGAGTGACTGCACCC[A/G]GCCAATATTGGGCAT	2186
rs544797457	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67926762	TTTTTTTTAGAGATA[A/G]GGGCTTGCTCTGTTG	2186
rs544799436	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67855628	TGGGCGAGGTCAGGA[C/G]ACAGTCTCAGGGTTT	2186
rs544823413	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67861169	CTCAAGCTAGAAATA[C/T]GAGAATAAACTTTTT	2186
rs544833285	snp	G/T	0.00557542	0.0525036	intron-variant, missense	BPTF	GRCh38.p7	17:67963348	GTTCTATATTGGCTG[G/T]GATCTTTGTACTAAC	2186
rs544836273	snp	C/T	0.0023933	0.0345097	intron-variant	BPTF	GRCh38.p7	17:67896119	AGGCACCCACCACTA[C/T]GCCCAGCTAATTTTT	2186
rs544843819	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67861019	TTCAGTTCTGTATGT[C/T]CAGCAGACTCCTGGA	2186
rs544861560	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67849157	GTTTTCAAACTTGCC[A/G]CACATCAGAATCATT	2186
rs544867539	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67974697	TCTCAAGGACACTGC[A/G]AAGGATTCCGATGAA	2186
rs544879165	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67916655	CCTGTAATCCCGGCT[A/T]CTCGGGAGGCTGAGG	2186
rs544894532	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67960760	GCCTACCTTAAGTGG[A/G]TACCTAATTGATTCC	2186
rs544905297	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67956040	GACAGGGTCTCGGGC[C/T]AGGCGCAGTGGCTCA	2186
rs544905785	snp	A/G	1.64735e-05	0.00286993	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67854616	AGAGGACGAGTGGCA[A/G]TGTGAAGTCTGTGTA	2186
rs544909995	snp	A/C	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67888106	ATCTACACTTCCATC[A/C]TTTGGTAGCTCAGCA	2186
rs544973813	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67967979	CCTTCTCCATTTACT[A/T]CTTCTTTTTCTGAAG	2186
rs544984804	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67833437	ACATCTGAACTGTTT[C/T]CACTTTTTGGCCATT	2186
rs545002840	snp	A/G	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67934858	GCCTGAGCAATGAGC[A/G]AAACTCTGTCTCAAA	2186
rs545003139	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67942641	ATCCCTAGAGAAGTT[G/T]TTGGCCATGTGAGCA	2186
rs545023766	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67857575	GGGCTCAAGCAGTCC[C/T]CCTGCTTCAGCCCAC	2186
rs545034616	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67967585	CAGCACTTCCGGAGG[C/T]CAAGGTGGATGGATC	2186
rs545044429	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67927792	TTTAATGTAATATAT[A/G]TGGTATAGAGACATG	2186
rs545057513	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67953054	CAAGCTCCGTCTCCC[C/T]GGGTTCACGCCAGTC	2186
rs545058233	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67837028	AGTTGTGAATCTTCT[C/T]TGTGTCTCAGAAGAA	2186
rs545085987	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67975586	TATTTTAGAACCTCA[A/G]TCAGAAACAAAATTG	2186
rs545095639	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67835720	GCCCAGGCTGGAGTG[C/T]GGTGGCGCGATTTCG	2186
rs545100921	snp	C/T	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67842661	TCCACAATGAAAATA[C/T]AAAACATGTCTCTAT	2186
rs545139422	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67876386	TGGTCAGCAGTGAGC[C/T]GTGTTGCTGAAAACA	2186
rs545161996	snp	C/T	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67826905	GTTAAGGAAACGGAT[C/T]ATTTGGGTTAGTAGG	2186
rs545179448	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67940390	TTATTTCAATTCAAA[A/G]TAATGCCAAGGGTGT	2186
rs545200747	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67869475	GTGATAGAACACTGC[A/G]TATTGGAGAATTAAG	2186
rs545230871	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67913269	CTCATTTTTAAAAAA[C/T]GAGATAATAGAGATA	2186
rs545231549	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67979993	TTGCAGATCGCACCA[C/G]TACACTCTAGCCTGG	2186
rs545272602	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67898510	AGATGGGGTCTCCCT[A/G]TGTTACTCAGACTGA	2186
rs545293126	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67949858	AGGTCAGTTCAAGAC[C/G]AGCCTGGCTAACGTG	2186
rs545334234	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67925547	AATACAATGTGCCAT[A/G]TGTGCCTAAACATTG	2186
rs545340029	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67861370	TTGAGATGGAGTCTC[A/T]CTCAGGCTGGACTGC	2186
rs545375320	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67973739	TCGGAACTCATGACC[C/T]TGGATGATACGCCCA	2186
rs545377100	snp	C/T	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67869988	CTGGGCGACACAGAG[C/T]GAGACTCCGTCTCAA	2186
rs545380952	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67925907	CAATCACTAAACCCA[A/G]ATATCTATAACAACT	2186
rs545398067	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67933254	AAAGAGTGAGACTCC[A/G]TCTGAAGGAAAAAAA	2186
rs545414774	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67918938	AGCACTTTGGGAGGC[C/T]GAGGCAGGTGGATCA	2186
rs545426346	snp	C/T			intron-variant, utr-variant-5-prime	BPTF	GRCh38.p7	17:67889867	AATTGATAGTCTGAC[C/T]AACTGCTTTGCTACC	2186
rs545466707	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67955696	GCCAGACATGGTGGC[A/G]GGCGCATGTAATCCC	2186
rs545486822	snp	C/G	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67883821	GGCCAGGCTGGTCTC[C/G]AACTCCTGAGCTCAT	2186
rs545514028	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67877120	AGGAGTTTGGTACTT[G/T]TGTAAAGTAGATAAA	2186
rs545550229	snp	A/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67919548	TGTCTCTTAAAAAAA[A/T]TTTTTTTTTCACATA	2186
rs545552169	in-del	-/TTTT			intron-variant	BPTF	GRCh38.p7	17:67881514	TTTTTTTTTTTTTTT[-/TTTT]GAGAGACAGAGTCTC	2186
rs545634730	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67868588	CTATAGTGCCTTTTA[A/G]GTTTTAGCTTAGATA	2186
rs545634902	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	BPTF	GRCh38.p7	17:67825081	TTTTTTCTTTCTCTC[G/T]CTGGCTCTTTCAGCA	2186
rs545642455	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67934010	GACCCTGCCATTGCA[C/T]TCCAACGTGGGCAAC	2186
rs545676888	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67890189	ACTGGTTTTGATAGA[A/G]ATACATCAAACTTGC	2186
rs545681586	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67980887	ATTAGGCTGTGTGCA[A/G]TGGTGCATGCCTGTG	2186
rs545730924	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67970124	TGTAATCCCAGCTAC[G/T]TAGGAGGCTGAGACA	2186
rs545800448	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67876394	AGTGAGCTGTGTTGC[C/T]GAAAACACCAGTTTA	2186
rs545803488	snp	A/G	1.648e-05	0.0028705	missense	BPTF	GRCh38.p7	17:67931996	GAAAGGCAATTATTC[A/G]AACACCTGTGATGGT	2186
rs545813149	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67895701	CTCTGGGCTCAAGCA[A/G]TCTGCCTGCCTCAGC	2186
rs545832619	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67855379	TGTTCCTCTATAGCC[G/T]AGCTCAGCTCATCCA	2186
rs545858416	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67934174	CTTTATAGTAAAGCT[A/T]GAAATTAATATTAAA	2186
rs545872790	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67868500	CAAGGGTTCTGCATC[C/T]TGAGAATACTGTATT	2186
rs545885580	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	BPTF	GRCh38.p7	17:67888987	GCCCAGTAACTTGCT[C/T]TAGGATCCATGAAGG	2186
rs545886364	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67967872	AATAGAGGAGTAGCT[A/G]TATCAGATGGTGTCT	2186
rs545958051	snp	A/G	0.00557542	0.0525036	intron-variant	BPTF	GRCh38.p7	17:67978381	TCGGCTCGCTGCAAC[A/G]TCTGCCTCCTGGGTT	2186
rs545995787	snp	C/G	2.54372e-05	0.00356622	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67826144	GGAAGAGGAGGACAT[C/G]GTCTCCGAGGAGGAG	2186
rs546018686	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67965510	AGAGACCAACCTGGG[C/T]AGCAAAGTGAGACCC	2186
rs546032270	in-del	-/AC	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67899011	ATTGTCAAGATATAG[-/AC]ACAATTATTATATGC	2186
rs546036124	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67971982	TTTGTCTTTGAGAAT[A/G]TTTATTTCAAAAGTA	2186
rs546038915	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67873513	TTATTCACAAATAGC[A/G]TACTCTAGTTGATAA	2186
rs546045494	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67866002	GCACATGTCTGTAAG[G/T]CCTAACTACTTGGGA	2186
rs546048963	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67910057	AGTGCCACCAGCTTA[A/G]TGGTCTACTTTCTGT	2186
rs546069540	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67960465	TTCCTCAAGCATAAC[A/G]TCCAACAGTTTGGCA	2186
rs546078333	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67902542	GCTCCCTTTCCCCTC[C/T]TCCCATCAGCTTATG	2186
rs546108527	snp	A/G	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67866769	GCAAAATTTGAAAAT[A/G]GATTAAAATTTTCAA	2186
rs546111324	snp	A/C	0.00279162	0.0372561	intron-variant	BPTF	GRCh38.p7	17:67966856	CCTGTAATCCCAGCA[A/C]TTTGGGAGGCCGAGA	2186
rs546130088	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67852964	AATATGGTGAAACCC[C/T]ATCTCTACTAAAAAA	2186
rs546166398	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67939649	TTGGGAGGCCAAGGC[A/G]GGTGGATCACGAGGT	2186
rs546183492	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67953320	GGACTGCAATGGCGC[A/G]ATCTCGGCTCCTGCA	2186
rs546206567	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67831842	TTGAGTGCCTGCTTA[C/T]GGTGGTTATGATCTC	2186
rs546225675	snp	C/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67908978	TAGCTGAGATCACAG[C/G]TGTGCACCACCACAC	2186
rs546260104	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67945273	GATCCTCCCACCTCA[A/G]CGTCCCAAGGTGCAC	2186
rs546261167	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67862588	CTTGGGCTGCTTGAC[C/T]AAGAGCTTAGGACCT	2186
rs546291396	snp	G/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	BPTF	GRCh38.p7	17:67889446	GATGTCTAAAAAGTA[G/T]CTATTACAGGACTTT	2186
rs546331272	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67845028	GATTACAGGCATGAG[C/T]CACTGCGCCCAGCCT	2186
rs546334139	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67846301	TTTAGAGCAGCCTGG[A/G]CAGCATAGAGGATAC	2186
rs546341790	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67938528	AAAGGAAGCAACACA[A/G]ATAGTTACAGAGGCA	2186
rs546356648	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67972980	TTTTTTCTTTAACTG[A/C]ATAAACTGGAGCTTT	2186
rs546386695	snp	A/G	0.00835141	0.0640778	intron-variant	BPTF	GRCh38.p7	17:67952979	TTTACTTTTTTTTTC[A/G]AGATAGAGTCTTGCT	2186
rs546392127	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67910300	CTCTTTTGGCTATAC[C/G]AATAATGCTGCTATG	2186
rs546393443	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67840030	TTGTCCCTAATGACA[A/G]ATGGTTCTGAGCCTC	2186
rs546394208	in-del	-/A			intron-variant	BPTF	GRCh38.p7	17:67849942	AAGACTCCATCTCAG[-/A]AAAAAAAAAAATTCA	2186
rs546429591	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67916652	GCGCCTGTAATCCCG[G/T]CTACTCGGGAGGCTG	2186
rs546450509	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67954220	TTTTTGTAGAGACAA[C/G]TTTTTGCCATGTTGC	2186
rs546466065	snp	A/G/T	3.30225e-05	0.0040633	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67903882	AACGATGCAGCAAGC[A/G/T]ACATGGGTAAAATAC	2186
rs546500200	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67858552	GGAGTGAGACTCTGT[C/T]TCCAAAAAAAAAAAA	2186
rs546520537	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67901155	ACAGAAGAAGCAAAT[C/T]AGTAGATAAAATACA	2186
rs546526496	snp	A/T	0.000798403	0.0199641	intron-variant, utr-variant-5-prime	BPTF	GRCh38.p7	17:67889819	ATCTCAAAAAAAAGA[A/T]AAAAAACCTCCATGA	2186
rs546529401	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67903080	GCCTGTGTCTCATGA[G/T]TTAGGTCAATATGGG	2186
rs546531290	in-del	-/A			intron-variant	BPTF	GRCh38.p7	17:67949575	GTGAGACTCCATCTC[-/A]AAAAAAAAAAAGTAG	2186
rs546588150	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67896446	ACAGTGTTTACTCTA[C/T]GGGTAATGAGTAACT	2186
rs546588637	in-del	-/A	0.00835141	0.0640778	intron-variant	BPTF	GRCh38.p7	17:67866841	AATGTGTCATTTGAC[-/A]AATGTCATCATTGTA	2186
rs546589360	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67946987	AGGAGTTTGAATGTG[A/G]ATTTTAAGTGTTACC	2186
rs546623630	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67979130	AGCCATCTTCATGCC[A/G]CTGCACTCCAGCCTG	2186
rs546630048	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67882747	CGTGGTGGCTGACGC[C/T]TGTAATCCCAGCACT	2186
rs546664426	snp	C/T	0.0126979	0.078662	intron-variant	BPTF	GRCh38.p7	17:67880962	TTATATATATATACA[C/T]ACACACACACACACA	2186
rs546671293	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67923268	TTGCTATGTTGTTCA[A/G]GCTGATCTTGAACTC	2186
rs546674693	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67854853	CTATGCTGTTGATGT[A/G]GTATAAACCTTTGTA	2186
rs546675127	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67953558	CCACCATGCCCGGCC[C/T]GTCAAATTGTTCTAT	2186
rs546692344	snp	A/C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67847015	TGGACTTGTGGGTTT[A/C/G]TTGTTGTTTTTTTGT	2186
rs546697957	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67971629	GCCAACATGGCGAAA[C/T]CCCGTCTCTACTAAA	2186
rs546740327	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67887796	CATATATTTATGTGT[C/G]TTAACCTCATTCTCT	2186
rs546760083	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67979499	CAGTGCACCAAGACC[A/G]CGCCACTGCACTCCA	2186
rs546767801	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67883013	GTCTAAAAAAAAAAA[A/G]AAAAAAAGAAAAGAA	2186
rs546815459	in-del	-/AC	0.0019968	0.0315343	intron-variant	BPTF	GRCh38.p7	17:67850892	AGGGGAGAAGAAAAG[-/AC]ACACACACAATACCT	2186
rs546818715	snp	A/G	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67874004	ATGCTGGATGGATGG[A/G]TGGATGGATGGATGG	2186
rs546836342	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67867669	CAGTTGGGAGGAGTA[A/G]TGGTTAGGTATTTTG	2186
rs546840188	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67972739	CCTTAAGGGATACCT[A/C]ATTAACTTGGAACCA	2186
rs546854045	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67960555	GGCACTAAACCGTAA[A/T]TGTAGTTTCATTTTT	2186
rs546856038	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67879993	CTATCCAAACTACAG[C/T]AGTGGGCTATTCATA	2186
rs546857276	snp	A/T	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67838842	CTAAATATTTTCACT[A/T]ATGCCATGAAATCAG	2186
rs546890235	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67895380	ATATATGTTTTTGAG[A/T]AAAGTACATTTATGC	2186
rs546924699	snp	C/G			upstream-variant-2KB	BPTF	GRCh38.p7	17:67824386	ATCCGGCCTTGGCCT[C/G]TCAAAGGACTGGGAT	2186
rs546926022	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67954829	CTCAAGGTTTTCTTT[C/G]TAACCTAGGAAGAAG	2186
rs546930554	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67972210	ATATTTGGATTGTTA[C/T]CAGTATTATTTAAGG	2186
rs546942131	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67860845	TTACAACAGGCGTGG[A/G]CCACCACACGCCTTT	2186
rs546976880	snp	C/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67965987	GATCACTTGAGCACA[C/G]GAGGTTACAGTGAGC	2186
rs546977580	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67906756	CACCAGTATCTTGCT[C/T]GCGACAGAATTATGA	2186
rs546982381	snp	G/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67851687	CAAACAGGTGTGCAG[G/T]CTGTTCAGTTATAAG	2186
rs546988907	snp	A/G			intron-variant, utr-variant-5-prime	BPTF	GRCh38.p7	17:67889661	AAAAATACAAAAATT[A/G]GCTGGGCATGGTGGC	2186
rs546989133	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	BPTF	GRCh38.p7	17:67824406	AGGACTGGGATTGCA[A/G]GTGTGAGCTACCACG	2186
rs546992317	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67844667	CGGCCTCCCAAAGTA[C/T]TAGGATTGCAGGGGT	2186
rs547037815	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67917419	TGAGCCACTGCGCCC[A/T]GCTGATATTGTCCTT	2186
rs547048119	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67873287	ACGTGGTGAAACCCC[A/G]TCTCTACTAAAAATA	2186
rs547053231	snp	C/T	0.00279162	0.0372561	upstream-variant-2KB	BPTF	GRCh38.p7	17:67825229	CGGTCCGCGGAGACT[C/T]TGGTCTCCGAAGGCC	2186
rs547069875	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67954626	CAGTTTTGTGTCTCT[A/G]TTCCATTGAGATTGT	2186
rs547073071	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67957512	TTGAAGACCAGCCTA[A/G]CCTACATGGTGAAAC	2186
rs547100829	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67923741	TGCCTCAGCCTCCCA[A/C]AGTGCTGGGATTACA	2186
rs547114004	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67966369	CCCAACACAAAGTCT[C/T]CTGACCAGCCTTTGA	2186
rs547120679	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67858028	CCTGACCTTGTGATC[C/T]GCCCACCTCAGCCTC	2186
rs547133306	snp	A/G			utr-variant-3-prime	BPTF	GRCh38.p7	17:67984244	TTTAAAATTTGTTGC[A/G]GCAAGAACTTTCCTA	2186
rs547151421	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67901239	CACAAAGGGAAAGCA[C/T]GTTTGGGAAGATATC	2186
rs547211087	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67839333	TTTCCTAAGTTTTTT[A/T]TTAAAAAAAAATCAG	2186
rs547211810	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67914966	TTCTGTCTAATGGAG[A/G]CATGGGTAAATATGT	2186
rs547228659	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67868488	GCATTCCATATTCAA[A/G]GGTTCTGCATCCTGA	2186
rs547255212	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67892165	TATTTTCTCTGTTTC[C/T]GAAACTGTAGTAGTT	2186
rs547256018	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67971071	AGCCTTCTGAGTAGC[A/G]GGGATGTAGTATACT	2186
rs547262989	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67831148	ATGGATTGACAAGGA[C/T]GAGATAGCTGGTGGG	2186
rs547266766	snp	C/T	0.00256082	0.035691	intron-variant, missense	BPTF	GRCh38.p7	17:67929010	CCAGCACAGGTCAGA[C/T]GTTCCAAATTACAGG	2186
rs547269065	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67931073	AGATCGAAACCATCC[C/T]GGTCAATATGGTGAA	2186
rs547276230	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67872436	TGTTTGAAAATGGCC[A/G]GGCGTGGTGGCTCAC	2186
rs547294620	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67976404	CTTGAACTTGGGAGG[C/T]GGAGGTTGCAGTGAG	2186
rs547333657	snp	A/C	0.0023933	0.0345097	intron-variant	BPTF	GRCh38.p7	17:67937772	TCTTCAGGTGTGCAC[A/C]GATCACACTGGAACT	2186
rs547343141	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67952543	GCTGGGATTCCAGGC[A/G]TGAGCCACCACGCCC	2186
rs547351804	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67917757	CCTGCCTTAGCCTCC[C/G]AAGTAGCTCGGATTA	2186
rs547358901	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67917662	TTAGAGACAGAGTTT[A/C]ACTCTTGTCGCCCAG	2186
rs547362947	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67836558	AATAGTGAATGACAT[C/G]TTAGCTCATCCTAAA	2186
rs547403244	snp	A/T	0	0	intron-variant	BPTF	GRCh38.p7	17:67922256	GCTGCTTCCTTGTGA[A/T]TGAATATATGGGAAG	2186
rs547471556	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67937839	ATGAGATCCGGCCGG[G/T]TACAGTGGCTCATGC	2186
rs547484248	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67899675	AGCTGGTATTATAGG[C/T]GTGTGCCACCACGAC	2186
rs547498592	snp	C/T			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67897272	CTTGAACCCGGGAGG[C/T]GGAGGTTGCGGTGAG	2186
rs547503474	snp	G/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67936103	TAGGAAATAATTTTC[G/T]TACTATAAAACATGG	2186
rs547509649	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67900561	ATAGGGAGACCCTGT[A/C]TCTACCAAAAATAAT	2186
rs547517258	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67932648	AGAGGTTGCAGTGAG[C/T]CAAGATCATGCCACT	2186
rs547551172	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67908305	CTGGGACTACAGGCT[C/T]GTACCACCATGACTG	2186
rs547562327	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67921750	CTTACTTAAAACAGC[A/G]GCCAGGTGCGGTGGC	2186
rs547582160	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67913516	ACTGCTCTGGGAACA[A/G]GATAACCACCAACTT	2186
rs547623510	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67893049	TATAAACTTGAAAAA[A/C]ATGATAGGTGAGTAA	2186
rs547631839	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67881753	TGATCTGCCCACCTC[A/G]GCCTCCCAAAGTGCT	2186
rs547663639	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67928863	TTAAAAATACAAAAT[A/G]AGCCACATTTCATGC	2186
rs547693096	snp	C/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67886721	TGGGGTTTTTTGAAA[C/T]ATAAACAGGATCATT	2186
rs547746458	snp	C/T	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67953459	GATAGGGTTTTGCCA[C/T]GTTGGCCAGCCTGAT	2186
rs547753898	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67879418	GTGCTGGGATTAGAG[A/G]CGTGAGCCACCGCGC	2186
rs547755018	snp	A/G	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67921760	ACAGCGGCCAGGTGC[A/G]GTGGCTTCCGCCTGT	2186
rs547768744	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67853173	ACAAAACTCTCAGTT[A/G]TTTATATTGATACAT	2186
rs547783085	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67957788	TTGAGCCTGGCAGGT[C/G]AAGGCTACAGCAAGC	2186
rs547805282	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67960100	TTATATTCTTTTCTG[C/T]CAAAAACAAGCTTTC	2186
rs547808698	snp	A/G	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67953079	CCAGTCTCCTGCCTC[A/G]GCTTCCCGAGTAGCT	2186
rs547818080	in-del	-/CT	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67897333	GCAACAAGAGTGAAA[-/CT]CTGTCTCAAAAAAAA	2186
rs547851877	snp	C/T	1.65048e-05	0.00287265	synonymous-codon	BPTF	GRCh38.p7	17:67975914	GTGTGCAGAAGTTCT[C/T]GAATCATTCTTTGTA	2186
rs547867626	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67923620	GAGTAGCTGGGATTA[C/T]GGGGGTGTGCCACCA	2186
rs547884562	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67843178	TATATAGATACATAT[A/T]GATATCTACATACAT	2186
rs547942997	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67957025	CGGTGGCTCACGCCT[C/G]TAATCCTAGCACTTT	2186
rs547957958	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime	BPTF	GRCh38.p7	17:67983015	GTCAATTACTCTGCA[C/G]CAGGCTAAAATGAGT	2186
rs547963515	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67870992	TAGCCAGGATGGTCT[C/T]GATCTCCTGACCTCG	2186
rs547970405	snp	A/G	0	0	intron-variant	BPTF	GRCh38.p7	17:67932136	TTAGTACTTCAAAGC[A/G]TACTAAATTTCTAAT	2186
rs547971499	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67922670	CATTTACTCACTTAC[A/G]TATTGTCTTTGGCTG	2186
rs547973542	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67900219	AAGCAATTCTCCTGC[C/T]TCAGCCTGCTGAGTA	2186
rs547981853	snp	A/G	1.69729e-05	0.0029131	missense	BPTF	GRCh38.p7	17:67945525	GCCCAGCCACAGACT[A/G]CTCAGCCTTCAGCTC	2186
rs547998137	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67856988	TCCTTGTTATCATTG[C/T]GTTTTGAGGATTGTG	2186
rs548031026	snp	A/G	0.00953873	0.0683987	intron-variant	BPTF	GRCh38.p7	17:67965119	GGCTGAGGCGGGTGG[A/G]TCACAAGGTCAGGAG	2186
rs548036086	snp	A/G	0.00478085	0.0486577	intron-variant	BPTF	GRCh38.p7	17:67923776	TGAGCCACCGCGCCC[A/G]GCCCTCTCTCTTATT	2186
rs548042168	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67964065	TACTAAATTAATGAA[A/C]TGGAATGTCAATCTT	2186
rs548045223	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67898921	AGTGATACCCTGTCT[C/G]AAAAAAAAAAAAAAA	2186
rs548070569	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67958922	CAGTGAGCTGAGATT[A/G]CACCATTGACAAGAG	2186
rs548077714	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67950374	AAAGTCAGAAACCAG[A/G]AACCCCAGTGATGCC	2186
rs548078462	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67863058	GTTTTCCAGGGCCAC[C/G]ATAACAAAGTACCAC	2186
rs548082241	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67866190	TTGTTACATTGATGA[A/T]CTTAAAGTTGGTTGA	2186
rs548133592	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67944847	TGGGCCAGATGACCC[A/G]GCTGATTTCCAGAGG	2186
rs548139361	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67863416	CAGCCTCCCAAGTAG[C/G]TGGGACTACAGGCAC	2186
rs548152268	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67893101	GTATATTTGAAGTAT[C/T]AATACATGAAAGCAG	2186
rs548164983	in-del	-/CTGC			intron-variant	BPTF	GRCh38.p7	17:67828565	GGAGTTTTGCTCTTG[-/CTGC]CTGCCCAGGCTGGAG	2186
rs548184581	in-del	-/A			intron-variant	BPTF	GRCh38.p7	17:67929267	TAGTTTCTCCTCAGC[-/A]AACCGAGCACCACGT	2186
rs548188553	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67963965	TAAAATCAATTGAAT[A/G]TTTCATATTTATCTT	2186
rs548211439	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67901344	AAAAACAAAAGAAAA[C/T]GTCAATAAGAAAGCA	2186
rs548229299	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67922315	ATTTTTTAAATCTTT[C/T]TATGAGGAGATTTTA	2186
rs548238793	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67920925	AAGAAATATATAAAA[A/G]GCCAGGTACAGTGGC	2186
rs548245272	in-del	-/T	0.00517822	0.0506191	intron-variant	BPTF	GRCh38.p7	17:67891721	TGCCATTCAAGGGCC[-/T]TTTTTTTATCTGTTT	2186
rs548270547	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67838054	CTAATGGTCAGGGGA[C/T]TGGCAAACTTGTTCT	2186
rs548338628	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67830183	CACTTTGAAATTAAG[C/T]ATTTGCTAATTTTAA	2186
rs548348351	snp	C/G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67902244	AGGGTGTCACTGCGC[C/G/T]GAAGTCCTTCAGACA	2186
rs548380401	snp	A/G	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67906996	CAAGAAACAGCCTGG[A/G]CAACATGGCAAATCC	2186
rs548449804	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67900173	GCAGTGGCGCCATCT[C/T]GGCTCACTGCAACCT	2186
rs548500992	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67865685	AGTGGGGACAGAAAT[A/C]CCATTATATGTGTTC	2186
rs548543658	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67874204	GGTCCTTCTGTATCC[C/T]GTGGTCTATAACATG	2186
rs548584243	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67944753	TGGGTCCAGAACCAC[G/T]TTGTTGACCTTCTGC	2186
rs548622886	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67857411	GTGATCTGTCTGCCT[C/T]GGCCTCCCAAAGTGC	2186
rs548636408	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67906524	TTATTTCACGAGGGT[A/G]CCAGGTGACATAGTG	2186
rs548642817	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67878355	ATACTATTATGAATA[A/T]TTTACATGTTTCTTG	2186
rs548643852	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67970493	GATAATAATATAGAT[C/T]TCTAAAACGTATTGT	2186
rs548656571	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67851521	AAGCAGCATGTTTTA[A/G]AAGTAGAAAGAGAAT	2186
rs548656761	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67843676	GTAGCACCTTTACTA[C/T]AGAGCAGTTCTATCA	2186
rs548681899	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67837449	GTCTTGCTCTGTCGC[C/T]CAGGCTGGAGTGCAG	2186
rs548718688	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67844192	TCAAGTGAGTCTCGT[A/G]CCACAGCCTCCGGAG	2186
rs548743190	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67976627	GGAGTTCAAGGCTGC[C/T]GTGAGCTGTGATTAC	2186
rs548763771	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67951640	CTCTAAATCTAACCC[C/T]CAAAGACAATCATTT	2186
rs548772537	snp	C/T	0.00358779	0.0422022	intron-variant	BPTF	GRCh38.p7	17:67981336	CCTTTGCCATATTTT[C/T]CCATTTTATGATCTC	2186
rs548773348	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67914631	AGTGACCTGGCAGTT[C/G]TGGAGGCCGACCTTT	2186
rs548778676	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67877508	AAGACATCTTACTTG[A/G]TTTTCTTTTCTAAAC	2186
rs548794075	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67964724	AGTTGTTCTTGGCCG[A/G]GCATGGTGGCTCATG	2186
rs548809881	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67903354	TTATGGCATATCCAT[A/G]CAATGGAATATTTTT	2186
rs548830761	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67921554	AAATAAATAAATAAA[A/T]AAAAAGATAATGTCC	2186
rs548857175	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67892190	GTAGTTAACAAGACT[A/G]AAAGTATTAGGCTTT	2186
rs548858602	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67857080	AATCACTTGTTCATC[C/T]ACTTTAAAATCTTTT	2186
rs548863133	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67943042	GCCTTATATATACCT[A/G]AGATACATACCGAAG	2186
rs548880095	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67972133	TTTCTGCTAATTTGG[C/G]AAAGAAAGTGTTTTT	2186
rs548881235	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67949435	CAAAAATTAGCTGGG[C/T]GTGGTGGCAGGCACC	2186
rs548882083	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67942059	AATCCCAGCACTTTG[G/T]GGGGCCAAGGTTTTG	2186
rs548906040	in-del	-/T	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67907933	GATTGCCTTTGATCC[-/T]TTTTTTCAGTCTTTT	2186
rs548907413	snp	A/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	BPTF	GRCh38.p7	17:67982103	TAGGTTAAAATTTTC[A/T]TAATCGTTCTTTTCT	2186
rs548916755	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67884974	TCATAGTTTGAATTG[A/G]GCATATTTCCATATG	2186
rs548940390	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67956048	CTCGGGCCAGGCGCA[A/G]TGGCTCACGCTTGTA	2186
rs548947475	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67836322	CAAATGGCAATGTTC[A/G]GTAGGTGCAGTTTAT	2186
rs548956658	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67856309	GTTTTTAGAATCTTC[C/T]TTTAAAAAAAATAGT	2186
rs549022549	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67828673	AGCTGGGATTAAAGG[C/T]ATGCAGCACCACGCC	2186
rs549107342	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67828817	ACAGGCATGAGCTAC[C/T]GTGCCTGGTCTGACA	2186
rs549138406	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67827105	AAAGTACAAAACTAC[A/G]GGAACGCGCGTCTTA	2186
rs549153527	snp	C/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67915576	CTGTACCTCTACACC[C/G]CTTCCCTCCAGTCAT	2186
rs549174726	snp	C/T	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67934518	GAGTGAAACTCTGTC[C/T]CAAAAAAAAAAAGAA	2186
rs549231452	in-del	-/T	0.400325	0.199756	intron-variant	BPTF	GRCh38.p7	17:67851273	TTTGCGATTTTCTGC[-/T]TTTTTTTTTTTTTTT	2186
rs549237058	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67862777	GGTGTCAGCAGGGCC[A/G]TGCTCCCTCTGCAGG	2186
rs549264919	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67961808	GCAAAACCCTGTCTC[C/T]ACTAAAAATGCAAAA	2186
rs549275193	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67826511	TAGATTTACAAGAGG[A/G]AAGAGGCGCATTGTT	2186
rs549278311	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67842290	TGCATGATACCTTTG[C/G]CCACTACATCCTTCT	2186
rs549298514	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67918532	CGTGTTATGCCTATG[A/C]ATGAAGAAGTTTTTC	2186
rs549377315	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67915890	GAATGAATGCTTGAA[C/T]GAGCAGACTTACCGT	2186
rs549377453	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67861576	CCACCTCAGCCTCCA[A/G]ATGTGCTGGGATTAC	2186
rs549423357	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67862271	GTGAGCCATCGTGCC[C/T]GGCCTAGTTACTTGT	2186
rs549441315	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67835647	TGTGATTAGAAAATC[C/T]GCCACAGTCCTGGTA	2186
rs549451169	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67868820	CCTGTGAATTCATGC[A/G]TATTTTTGGAGAATG	2186
rs549457604	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67843688	CTATAGAGCAGTTCT[A/G]TCACCTTTGGGTGTG	2186
rs549536305	snp	A/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67837316	TAGGACTGGGATTGG[A/T]TTGTTGCATTATAGT	2186
rs549537431	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67905550	CATCTCTACAAAAAC[G/T]TTTTAAAAATTAGCC	2186
rs549567390	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67975136	GACAAAAACCAAATA[C/T]ATATTTCACAATATC	2186
rs549604493	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67958354	AAAAACAGAGTACAG[G/T]AAAGAAGCTGGCCAA	2186
rs549619473	snp	G/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67871212	ATTAAAAATTTCAAA[G/T]GTACACAAAAGTTGA	2186
rs549638821	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67917325	AGATGGGGTTTCACT[A/G]TGTTGGCCAGGCTGG	2186
rs549652014	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67837772	AGACCTTTAGCAGGT[A/G]TTCTTGGATACTGAC	2186
rs549666354	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67885608	AAGAAGTTAACAATC[A/G]CATTTAGGCATTACC	2186
rs549672334	snp	A/G	0.00438332	0.0466095	intron-variant	BPTF	GRCh38.p7	17:67875882	ATCCCCATTTGCTAA[A/G]TTGTCACCTAACATT	2186
rs549674262	snp	G/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67883255	CAGGAGGCAGAGGTT[G/T]CAGTGAGCTGAGATC	2186
rs549681221	snp	C/T	0.000798403	0.0199641	intron-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67919028	ATACAAAAAATTACC[C/T]GGGCGTGGTGGTGGG	2186
rs549694467	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67936032	TTGCCATAATGTTAC[C/G]TATAGCAAGGAATTA	2186
rs549698684	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67904153	CCTGCCTCAGCCTCC[C/T]AAGTAGCTGGGATTA	2186
rs549703994	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67975731	TTCACATTGGAAAAA[A/C]CTTAAAGCTCTGAAA	2186
rs549705790	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67957941	ATGGGTTTGTTCCTA[C/G]GGTAATAAGGTTTGC	2186
rs549705968	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67968840	ATACAAAATTAGCCC[A/G]GCGTGGTGGCACATG	2186
rs549712693	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	BPTF	GRCh38.p7	17:67982948	GCATAAAGGTTGGGC[C/T]AAGTGGTCCTGGACT	2186
rs549730440	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67950327	AGACTAATAATACTA[C/T]CTATCTGTGAAACAT	2186
rs549733013	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67980443	GGACAGAGGAGCACA[A/G]CTTCTCATTATAAGC	2186
rs549735457	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67876576	TTTGGGAGGCCTAGG[C/T]GGGCAGATCACCTGA	2186
rs549739694	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67829469	AGTTCCCTCCCCTTG[A/C]CCCCCACCCCCCGGA	2186
rs549751020	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67842421	AACTTTCCCCTAATT[A/G]TCAGTTGTCTGAGTT	2186
rs549754317	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67891572	TGTAGCAGCTCTTCC[C/T]GTTTTCAAACAGATG	2186
rs549798016	snp	C/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67914781	GCTGAATTTCTGGAG[C/G]TGAATTTCATGTCTT	2186
rs549801489	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67900915	TTGGGAGACTGAGCC[G/T]AGAAGTTGGAGGAGG	2186
rs549820022	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67899821	AGCATGAGCCACCGC[A/G]CCCGGCCTATGCTGA	2186
rs549831726	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67927996	TCAAGCAATTCTTCT[G/T]CCTCAGCCTCCCGAG	2186
rs549852276	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67885888	AGGTGATACGAGTCA[A/G]TGAGTTAGAGTTGGG	2186
rs549872203	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67942198	GTGTACGCCTGTAAT[C/T]CCAGCTGCTTGGGAG	2186
rs549892672	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67848547	TCTCAGAATTTCAGC[A/G]AAGTAAGGCAATTTC	2186
rs549895276	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67936973	AACAATTATTCAGTA[C/T]TACCTATGTGCCAGA	2186
rs549897073	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67874084	TGGCCAAAGCTGAAA[C/T]AATTTGTGCAACAAA	2186
rs549911617	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67906370	AGGTGTGACCACTGC[A/G]CCTGGCCTATAAATA	2186
rs549922206	snp	A/G			synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67894112	CATTTTGGAGTGTGC[A/G]GTTAAACCAGTTGTG	2186
rs549934052	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67956950	GCCTGGGAGATAGAG[C/T]GAGACTCCGTCTCAA	2186
rs549934502	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67927080	AAAATTGGACGTGAT[A/G]TCATAGGTGAGCAGG	2186
rs549996415	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67935191	CACTTTGGGAGACTA[A/C]GGCAGTCAGATCACT	2186
rs550031458	snp	A/G	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67885134	ATTTTTAGGTGATTT[A/G]AAGAGTATCTTGTCA	2186
rs550093091	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67878380	TTCTTGTGCACATAC[A/G]TGTGCATTTCTGGAG	2186
rs550104031	snp	A/T	1.67733e-05	0.00289592	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67912027	TGATCAAATAAAGCT[A/T]AAAAATACCACTGAC	2186
rs550124061	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67920857	AGATTGAAAATATAT[A/C]AATTCCATTTTATTT	2186
rs550124861	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67961870	TCCCAGCTACTCGGG[A/G]GGCCGAGTCAGGAGA	2186
rs550170363	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67872910	AACATAGTGAGACTC[C/T]ATCTCTATTTTAAAA	2186
rs550170604	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	BPTF	GRCh38.p7	17:67983529	TTTGTTTTCTGTTTG[C/T]TGGTTTGTTTGTTTC	2186
rs550200369	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67828093	CCCACCAGCACACCC[A/G]GCTAATTTTTGTATT	2186
rs550203540	snp	G/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67895865	ACAGTAGAGAGACTT[G/T]TACCCTGTGTACATG	2186
rs550205984	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67897658	CTTAGTAGGGCAGAA[A/G]CCACACTCTTAGGCA	2186
rs550221253	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67926197	GTTTTTTGTAGAGAT[A/G]GGACTTTTGCCATAT	2186
rs550239359	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67862343	ATGACAACTATGTAT[A/T]TGATACCCATGAAGT	2186
rs550304507	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67962510	CCCCTTGCCAAGCAG[C/T]GTAGACCCTCACAGG	2186
rs550342216	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67891571	TTGTAGCAGCTCTTC[C/T]TGTTTTCAAACAGAT	2186
rs550343517	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67862955	CTAACAGTTCTTCAG[C/T]CTCTTCCCATTACCC	2186
rs550387600	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67882873	CGTGGTGGTGCTTGC[C/T]TGTAGTCCTAGCTAC	2186
rs550420842	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67905723	CTTAAAAAAAAAAAT[C/G]TTAATTCAGTACTAA	2186
rs550430469	in-del	-/A	0.425725	0.177823	intron-variant	BPTF	GRCh38.p7	17:67835213	AGAACCCATCTCTTA[-/A]AAAAAAAAATTTAAG	2186
rs550465882	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67869661	GTTATATAGTTCAGT[A/G]TGATTCAGCATGTAA	2186
rs550483081	in-del	-/G			intron-variant	BPTF	GRCh38.p7	17:67955217	CGGGAGGCAGAGCTT[-/G]CAGTGAGCCCAGATA	2186
rs550505657	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67896567	AGGATAAATCTATAT[A/G]CTACATACATTTATG	2186
rs550527361	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67870178	TACTACATGGAGTAC[A/G]TGGAAATAAGGTGAG	2186
rs550550514	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67980243	CCAGCTACTGGGGAG[A/G]CTGAGGCAGGAGAAT	2186
rs550566918	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67890433	ACTTCTGATTTACAC[A/C]CTTCCTGCTCATTAG	2186
rs550571861	in-del	-/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67882207	CCTGACTTGGAATCA[-/T]TTTTTTTTCCTCCAA	2186
rs550581041	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67827250	TCTAAGTCACACGGC[A/G]TCAGTATCAGATTTA	2186
rs550586504	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67973759	TGATACGCCCACCTC[A/G]GCCTCCCAAACTGCT	2186
rs550599474	snp	A/G	6.6012e-05	0.00574471	synonymous-codon	BPTF	GRCh38.p7	17:67940512	CTCCGCCCCTAACAC[A/G]GTTTCCTCAACACCT	2186
rs550609367	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67877084	AAGACTTTATTAAAT[A/G]TATCATACCAGATTT	2186
rs550612464	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67939773	TAGTCCCAGCTACTC[A/G]GGAGGCTCAGGCAGG	2186
rs550628353	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67903210	GAGTGCTTTAAAATC[C/T]GCAGTGCTTGTGAGA	2186
rs550634568	snp	C/T	1.65395e-05	0.00287567	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67874971	GTCCCTTGAAAAAGA[C/T]AGTGACGACAAAACA	2186
rs550651677	snp	G/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67960601	ATTTTACAAAATATT[G/T]AACTTCTACTTTGAA	2186
rs550652529	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67845384	TTCTATCATTTCTTT[A/G]TTAATTATCTGGCAT	2186
rs550672804	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67974544	CTTCAGATGCCGGTC[A/G]CCAGCCCCAGGTGGT	2186
rs550675199	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67967745	AATCACTTGAACCCG[C/G]GAGGCAGAGGTTGCA	2186
rs550683648	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67880603	GCTTAATATTCAAAC[A/G]TTTGTAGGTTTTTGT	2186
rs550699908	snp	A/G	0	0	intron-variant	BPTF	GRCh38.p7	17:67860908	CGAATCAACTAAACT[A/G]TGCTTTTAAATCTAT	2186
rs550701808	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67841406	AAGAGCGAAAATCTG[G/T]CTCAAATAAATAAAT	2186
rs550715144	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67849656	GAAATGCAAGTTCTC[A/G]GCTGGGCGTGGTGGC	2186
rs550733827	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67973917	GTTTTGAACTTGTCT[A/G]CGTTAGTGTTTGTGT	2186
rs550751598	snp	A/C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67968288	AAGTGGAAATAAATG[A/C/G]AAACTATCTCTGAAA	2186
rs550763390	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67978142	TACGGGCGTGAGCCA[C/G]CGCACCCGGCCATGA	2186
rs550769758	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67874138	ATAACCCAAAGAATA[C/T]AATTAATATCCATGA	2186
rs550792130	snp	A/C/G			intron-variant	BPTF	GRCh38.p7	17:67831207	CAGGAGGCACTTTAG[A/C/G]GTTCTTCAGGCCTTG	2186
rs550801481	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67941133	AACAGGATTATTTGC[C/T]CTATATATGATAACT	2186
rs550813021	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67861313	TAAAGTAGTGTAACC[C/G]CCTACCCCAACCTTC	2186
rs550822970	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67954859	GTTCAGTCTCTCTCT[A/G]TAAATAGAGAAGGGC	2186
rs550837691	snp	A/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67848185	TCTTTTTTTTTTTTG[A/T]ATTAGTACAATAAAT	2186
rs550841454	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67840843	GCTGGAATTACAGGC[A/G]TGAGCCACCATGCCC	2186
rs550843277	snp	G/T	0.00279162	0.0372561	intron-variant	BPTF	GRCh38.p7	17:67972289	CACCCAGGCTGGAGT[G/T]CAGTGTCGTGATCTT	2186
rs550863127	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67832194	TACCCGGCCTCTAAT[G/T]TTTTTCATGCTTTTG	2186
rs550896652	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67948567	ATTGTTGAAAAACTC[C/T]GAGAAGAGCTTTTCA	2186
rs550900401	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67971716	AGCTGAGTCAGGAGA[A/T]TTGCTTGAACCCAAG	2186
rs550903226	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67967031	CTTGAACCAGGGAGG[C/T]GGAGGTTGCAGTGAA	2186
rs550910143	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67888539	AGGTTGCAGTGAGCC[C/G]AGATCGTGCCACTGC	2186
rs550942877	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67937890	GAGGCCAAGGCGGGC[A/G]GATCACCTGTGGTCA	2186
rs550998827	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67827150	TTTGCCTTGCTTGGG[A/G]AATGCAGTTTCGTGT	2186
rs551010201	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67858070	GGATTACAGGCGTGA[A/G]CCACCGTGCCCGGCT	2186
rs551064504	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67943608	ATTTGGCACGTATTG[A/G]AAGACAAAATTCAGG	2186
rs551084825	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67954350	GGTTGTCTTTTTTTC[A/G]TATTACATGTTTTCC	2186
rs551107696	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	BPTF	GRCh38.p7	17:67889314	TTGCACTAAATTTAG[C/T]AAGTGATAAAGGATT	2186
rs551124065	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67839764	CTAAACGTTTCCATA[A/G]TGGTTTTGTATGAAC	2186
rs551140763	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67938735	CAATAATTAAAGCCA[A/G]AATTTTTAAAAAGAC	2186
rs551163024	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67882065	GTCTCGAACTCCTGA[C/G]CTCAGGTGATCCGCC	2186
rs551176870	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67883603	TTTGTTTTGTTTTGT[G/T]TGTGTGTGTTTTTTG	2186
rs551183337	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67931196	CTTGAACCCGGGAGG[C/T]GGAGGTTGTAGTGAG	2186
rs551200108	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67827379	ACAGAAAGTTTCTCT[A/G]GGCTGGTGCCGAGAT	2186
rs551214983	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67856468	TGGTTTTTCTATTTC[A/G]TATTCAGATGTTTAT	2186
rs551305105	in-del	-/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67895675	TTATGTTGCCCAGGC[-/T]TGTTCTTGAACTCTG	2186
rs551309585	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67890560	CTGTGGCCAGCTAGT[G/T]GTGTGCTTTGTCTGG	2186
rs551320244	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67931610	ACTCCACATTTTCCT[A/G]TGAGCACTAGTTACA	2186
rs551335376	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67842227	TATATACATAGACAT[A/G]TATCTACATACATTG	2186
rs551339309	snp	A/G	0.0107246	0.0724382	intron-variant	BPTF	GRCh38.p7	17:67847290	GAAGCCGAGGTGGGT[A/G]GATCACCTGAGGTCA	2186
rs551341308	snp	C/T	0.0341408	0.126114	intron-variant	BPTF	GRCh38.p7	17:67925758	AAACTAGTTTTCCCT[C/T]TCATTTTATAAAACA	2186
rs551352736	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67862225	AGGTAATCCACCTGC[C/T]TCGGACTCCGAAAGT	2186
rs551353091	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67968253	GTGTTTCATGGCAGC[A/G]TGAAAGAGGGGGAAA	2186
rs551358873	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67967056	AGTGAACAGAGATCG[C/T]GCCACTGCACTCTAA	2186
rs551362124	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67870245	AAAATGACATAAATA[C/T]TTTTTTCTTTCTTTC	2186
rs551368062	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67973985	TTAGAATATTTTTTA[A/G]TGTCTGACAGATAAG	2186
rs551413052	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67941911	GAGAGTGAAGAAAAT[G/T]AGAAAAGAACCAACC	2186
rs551415706	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67852182	ATTTAGTATAATGAC[G/T]TTGTATTTATACAAG	2186
rs551422642	snp	G/T	0.0023933	0.0345097	intron-variant	BPTF	GRCh38.p7	17:67828691	GCAGCACCACGCCCA[G/T]CTAATTTTGTATTTT	2186
rs551428165	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67868734	TTGCTTAAAAATAGA[A/G]TGTTTATATTTAATA	2186
rs551431472	snp	A/G	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67980385	ACTGAAAAGTCAAAG[A/G]GATTGATCATAGGGA	2186
rs551453438	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67975488	CATGTCGGTGTGTTT[A/C]CTTGATTTCAAACCA	2186
rs551474262	snp	A/G	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67854996	TTGATGCCTAGGCTA[A/G]GAAATAGAATGTTTC	2186
rs551474958	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67919828	TTAGGAATTTGCAGC[A/G]AGGAAGAAGCTCAGT	2186
rs551497488	snp	C/T	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67962808	TGACCATTTATCTTC[C/T]ACACCTGGCTGACCT	2186
rs551517396	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67961314	TATTAACACTTTAGT[A/G]TACCAGGTTCATTCA	2186
rs551556802	snp	G/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67896621	AACACAATGTTACAG[G/T]ATTGTTTAGGGATAT	2186
rs551564123	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67897173	CTCTACTTAAAAAAA[A/C]CAAAAACAAAAAACG	2186
rs551565458	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67868023	CTGCACAGGAGATGT[A/G]TTTATTTTTTCAGGC	2186
rs551619546	snp	A/T	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67904027	AGTCTTTGTATTTTA[A/T]TTATTTATTTATTTA	2186
rs551640092	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67981188	CAAAACAAAATTACA[A/G]TGTAAAGAGTTGTAT	2186
rs551640582	snp	A/C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67835338	GCATTTGGGGCATTT[A/C/T]ATATCATTGCAGAAA	2186
rs551645902	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	BPTF	GRCh38.p7	17:67825377	GCGCCCAGGGCTCCC[A/C]GCCCCCGACTCGACG	2186
rs551653549	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67967100	TGAGACTGTCTCAAA[A/T]AAATAAATAAATAAA	2186
rs551659644	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67833076	TGCTGGGATTACAGG[C/T]GTGAGCCACTGCGCC	2186
rs551666435	snp	A/G	0.00517822	0.0506191	intron-variant	BPTF	GRCh38.p7	17:67924103	TCCCAGGTTCAAGCA[A/G]TTCTCCTGCCTCAGG	2186
rs551668008	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67848245	GGTTTCTGGGATTTG[A/T]TCTTGGCATGACTTT	2186
rs551668474	snp	C/T	0.0107246	0.0724382	intron-variant	BPTF	GRCh38.p7	17:67832183	GTGAGCTGCCGTACC[C/T]GGCCTCTAATTTTTT	2186
rs551707277	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67941089	TTATATGGAGGTACA[A/G]AGTATTAAGAATATC	2186
rs551725079	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67937920	AGGAGTTCAAGACCA[A/G]CCTGGCCAACATGGC	2186
rs551732207	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67931839	GAATGTTTAAAGATC[G/T]TGTGTTCTAAGTCCA	2186
rs551736648	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67937467	TGGGAATGATTTGCA[G/T]GGAGGGTTGAAATTT	2186
rs551743423	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67839381	TGTCACATGTCATCT[C/T]AGCATCTTTTAAGAT	2186
rs551744056	snp	A/G			missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912074	ATCGAGAGTCTGAAA[A/G]GAAAGGACAGAGAAC	2186
rs551749708	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67949279	CTAAGGCAGGATGAT[C/T]ACTTGAACCCGGAAA	2186
rs551801347	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67858511	AATGAGCCGAGATGG[C/T]GCCACTGTACTCCAG	2186
rs551811883	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67835158	GAGGCCCTAGTCAGC[C/T]ATGGACCATGCCACC	2186
rs551826024	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67904637	GTAAAAATGCATAAA[A/T]CCACATGTGGTTTAT	2186
rs551860824	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67955454	TTTTGGCAGGGGGGA[A/G]TCAGGTTTTCCTGTG	2186
rs551912064	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67972888	TCCTGAACACCTTAC[A/G]TGAACCTACAGCATC	2186
rs551912950	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67947996	AGAAAGTTTTTGTCT[C/G]ATCTGTAGAGGCATA	2186
rs551946405	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67853297	TCTGTTGTCTGTTTC[C/T]TAGGTAAGCCACTTT	2186
rs551960032	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67975718	ACTTCGGAGAATATT[C/T]ACATTGGAAAAACCT	2186
rs551973138	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67978958	GAGGCAAGAGGATGC[C/T]TGAGCCCAGGAATTC	2186
rs551973436	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67979460	GCTGAGACAGAATCA[C/T]TTGAACCTGGGAGAC	2186
rs552021636	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67979570	AAAATAATGACATTG[A/G]TTTTCGACTTTTAGA	2186
rs552094500	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67882627	ACTGAATGGCATTTA[C/T]GACTTTTTGCTGCTC	2186
rs552099508	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67867363	ACTTTAAATTTTAGA[A/G]TATTTTTAGATTTAT	2186
rs552114174	snp	C/T			intron-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67929794	CCACCCACGGAAGTG[C/T]GCTGTGCAGGCTCGC	2186
rs552123603	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67917672	AGTTTCACTCTTGTC[A/G]CCCAGGCTAGAGTGC	2186
rs552135525	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67869300	AAAAACAAAAAAATA[-/T]TTTCTGTGTGTTAGA	2186
rs552146934	snp	C/T	0.077417	0.180873	intron-variant	BPTF	GRCh38.p7	17:67843173	CTACATATATAGATA[C/T]ATATAGATATCTACA	2186
rs552164253	in-del	-/TA			intron-variant	BPTF	GRCh38.p7	17:67935779	GAATTGCTTGAACCC[-/TA]TAGAGGCAGAGGTTT	2186
rs552165061	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67839952	ACTTGATATTGTCAG[-/T]TTTTTTTTTTAAAAG	2186
rs552180636	snp	A/G	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67954073	CACACCACAGCTTCC[A/G]CCTACCCAGATCAGT	2186
rs552181337	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67953572	CCGTCAAATTGTTCT[A/G]TAATTTTTTTTTTTT	2186
rs552209695	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67895995	TTGAGACGGAGTCTC[A/G]CTCTGTCACCCAGGC	2186
rs552210439	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67916521	CTTGAACCCGGGAGG[C/T]GGAGGTTGCAGTGAG	2186
rs552214717	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67923214	GTGCATGCCACCACG[C/T]CCAGCTAATGTTTGT	2186
rs552216614	in-del	-/AGAT	0.00438332	0.0466095	intron-variant	BPTF	GRCh38.p7	17:67907880	CCCTGGTTGTCTTAG[-/AGAT]AGATACCTTTTTACT	2186
rs552220324	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67909276	CACCAGGTCCCCCCC[C/T]CCCTTTTTTTTTTTA	2186
rs552233247	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67887782	ACCTTTTAGGTCTAC[A/G]TATATTTATGTGTGT	2186
rs552271541	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67930324	CTGCCTCAGCCTCTC[A/C]AGTAGCTGGGATTAC	2186
rs552272446	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67853849	TAAAGAAATGTACTT[A/T]TGTATTTTAGGGGGG	2186
rs552273815	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67922688	TTGTCTTTGGCTGCT[C/T]TCATGATACAAAGGC	2186
rs552276765	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67927457	TATTTTTCTGTAAAA[A/G]TATTTGAATGTATAA	2186
rs552293735	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67873208	CACGCCTGTAATCCC[A/G]ACACTTTGTGAGGCT	2186
rs552316199	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	BPTF	GRCh38.p7	17:67823677	TTTGTCACCCTTAGA[C/G]CTCGACCAAATTGTA	2186
rs552336463	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67949916	AAATTAGCCGGACAT[A/G]GTGGCAGGTGCCTGT	2186
rs552336600	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67937127	AATATACTGTATAAT[A/C]ATGTATGAATTTTAC	2186
rs552348578	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67908689	GAGGCGGGGTTTCAC[C/T]ATGTTGGCTAGGCTG	2186
rs552381373	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67958993	TATCTTTTAAAAAAA[G/T]AAAATAGTGCGTTAT	2186
rs552417996	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67965759	TCAAGTGATACAGAT[G/T]TACTGAAGACACAGA	2186
rs552432929	snp	A/T	0.0023933	0.0345097	intron-variant	BPTF	GRCh38.p7	17:67880225	CATTAGTCTTTTTTT[A/T]AAAAAACACAACTTT	2186
rs552438146	snp	A/T	0.000798403	0.0199641	upstream-variant-2KB	BPTF	GRCh38.p7	17:67824303	CGGCTAATTTTTCAA[A/T]TTTTTTCTAAAGACG	2186
rs552481939	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67829304	CTTTTGCAACACATT[A/C]TTTTTAAAGATTATG	2186
rs552482528	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67878227	ATGTTGCTAGTAGTA[A/G]CAGCTTATTCTTTTT	2186
rs552484360	in-del	-/T	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67839609	TGTATTTGAGATTCA[-/T]CTATGTTGTTGTGTG	2186
rs552485995	in-del	-/T	0.00106767	0.0230802	intron-variant	BPTF	GRCh38.p7	17:67945389	GAGTAATAGAAATGG[-/T]TCATCTTTCCTTTTT	2186
rs552502920	snp	C/G	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67900374	CTTCCCAAAGTGCTG[C/G]GATTACAGGCGTTAG	2186
rs552527016	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67858786	ATGCTCCAATTCTCC[C/G]ATTCCTGTGCCTTCC	2186
rs552529693	snp	A/G	0.00011537	0.00759418	missense	BPTF	GRCh38.p7	17:67931933	CAGGGCCTCAGATTC[A/G]CCCTGGTATGACCGT	2186
rs552533074	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67866939	GGCTGCAAACCTGTA[C/T]GTCATGTGACTGTAC	2186
rs552535914	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67833131	ATTTCTTATAAAGTG[C/G]AATCATATAATATAT	2186
rs552536002	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	BPTF	GRCh38.p7	17:67824879	CCGGGCGTGGCAGCC[C/T]GGGGCGTGGCTCCTG	2186
rs552539544	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67965191	TACTAAAAATACAAA[A/G]AATTAGCCAGGTGCG	2186
rs552543639	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67849877	ACCTAGGTGACAGAC[A/G]TTGCAGTGAGCTGAG	2186
rs552553185	snp	C/T	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67828221	AGGTGTGAGCCACCG[C/T]GCCCAGCCTAGTACG	2186
rs552555852	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67976059	TTATGGTAAATTTAA[C/T]CTTAAATATCTTTAA	2186
rs552556042	snp	C/T	0.00557542	0.0525036	intron-variant	BPTF	GRCh38.p7	17:67857880	GCAACCTCCATCTCC[C/T]AGGTTCAAGCGATTC	2186
rs552584367	snp	A/G	1.64887e-05	0.00287125	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67929434	CCCAGGACAGCAACA[A/G]TCACAATTAGGCCCA	2186
rs552591021	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67931366	TAGTCCTAGCTTCTT[A/G]GGAGGCTGAGGCAGG	2186
rs552608123	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67831572	ATGTTAAGACCAGGA[A/G]CTCTGGTCTCTTCTG	2186
rs552666754	in-del	-/AAT	0.0166325	0.0896639	intron-variant	BPTF	GRCh38.p7	17:67883316	CGAGACTCCATCTAA[-/AAT]AATAATAATAATAAT	2186
rs552669860	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67923542	GGCTGGAGTGCAGTG[A/G]CATGATCTCGGCTCA	2186
rs552671321	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67832529	ATATTTATGAAAATT[C/T]AGTTTTTAAAAGGTA	2186
rs552682531	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67971546	CACGGTGGCTCATGC[C/T]TGTAATCCCAGCCCT	2186
rs552701141	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67965290	GGAGGTTGCAGTGAG[C/T]CAAGATCGAGCCACG	2186
rs552714254	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67937575	GAGCTGTGCAGATAT[C/G]TGAGGAAAGAGTCTT	2186
rs552752666	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67902464	GAGCTAGTCCTTCTC[C/T]TTAGTTCCAAGCGTG	2186
rs552759736	in-del	-/AGC	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67841473	TTAGTATTTTATATT[-/AGC]AGTAATATAATACTT	2186
rs552774800	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67943852	TGGGGACTTTAGTTA[C/T]TCAATACCTTTATTT	2186
rs552820591	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67976858	AGTGAATAAATTAAA[C/G]CCCCTGCACTCTATG	2186
rs552833244	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67966191	TGTTATCTAACATCA[C/T]GTCTCTGCTACCTCA	2186
rs552833770	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67952514	GTGATCCTCCCTCCT[C/T]GGCCTCCCAAAGTGC	2186
rs552836995	in-del	-/AT	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67835570	ATAAGATTTGGGGTC[-/AT]GTGTGAGATGACTTT	2186
rs552850847	snp	C/G	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67938155	AATTTCCATTTTGAT[C/G]TAAAAATAAATTGAT	2186
rs552852262	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67838270	TTTTGAGCTCTTGAC[A/G]TTCATTAGTCTGTGA	2186
rs552853672	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67888230	TCAAAAACCTCTTTC[C/T]CACAGTTACATCCTG	2186
rs552883501	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime	BPTF	GRCh38.p7	17:67983752	ATATTAGCTTTGTCC[A/T]ACCAACTTCTGGAAT	2186
rs552894572	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67895618	CAGACGCATTCCACT[A/G]TGCCTGGCTAATTTT	2186
rs552907751	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67944524	AGCCTCACAACGTCT[C/T]GAAGCTTTTGTACCC	2186
rs552927746	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67945133	CTTGAACTCCTGGAC[A/G]CAAGCAATCCTCCCA	2186
rs552987577	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67839484	TTATAATATTGATCC[A/C]CCCTTACATTCCTGC	2186
rs552999507	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67932869	AAGAAAAGACAAGGA[C/T]GGCCCTACTGATACT	2186
rs553010403	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67966735	AATTAATATCTTAGA[A/G]TATTTTTAGCAAGGC	2186
rs553015982	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67875279	CCCTATGAAAAAGAA[C/T]TATTCTTTAATATTA	2186
rs553020893	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67964999	GTGAGACTCCATCGC[A/C]AAAAAAAAAAAAAAA	2186
rs553036167	snp	A/G	0.0111196	0.0737302	intron-variant	BPTF	GRCh38.p7	17:67909260	GTGGCATGAGCCACC[A/G]CACCAGGTCCCCCCC	2186
rs553046873	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67924221	CGGCCTCCCAAAATG[A/C]TGGGATTACAGGCAT	2186
rs553082102	snp	A/C	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67872942	GGATTAAAAAATTAG[A/C]CAGGCGTGGTGACAC	2186
rs553102579	snp	C/T	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67879786	GTGGCAGATGACAGG[C/T]TCTTTTTCTAACAGT	2186
rs553122858	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67845486	ATTCATTGTGAAAAA[C/T]AAGAGGGCAGGCATG	2186
rs553153072	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67874214	TATCCCGTGGTCTAT[A/G]ACATGCCATAGTATC	2186
rs553154646	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67882201	ACCTATCCTGACTTG[A/G]AATCATTTTTTTTTC	2186
rs553159162	in-del	-/T	0.0111196	0.0737302	intron-variant	BPTF	GRCh38.p7	17:67953422	ACTGCACTCGGCTAA[-/T]TTTTTTTTTGTTTTT	2186
rs553172392	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67966953	AAAAATACAAAAATT[A/G]GCTGGGCATGGTGGT	2186
rs553184510	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67977266	ACGCCTGTAATCCCA[A/G]CACTTTGGGAGGCCA	2186
rs553208647	snp	G/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	BPTF	GRCh38.p7	17:67888794	AACATATAAGAAGAT[G/T]CCCCTTCTGGAGGCC	2186
rs553219042	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67850357	TTAACTTTTCTTTTG[C/T]CTCATGGTGTTTTTG	2186
rs553270091	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67896032	GCAGTGGCGTGATCT[C/T]GGCTCACTGCAGCTC	2186
rs553281715	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67958961	CATCTCAAAAAATAT[A/G]TATATGAAAAGAAAG	2186
rs553287457	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67869049	AGTAACACAATCTCC[A/G]TCTTACTCTCCCCCC	2186
rs553294188	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67952825	TAGTTACACTGCCCT[A/G]ACAATCCCGTGTGCC	2186
rs553299466	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67976908	GGGACAGTTGATAAA[C/G]ATCATAAACCAGGTA	2186
rs553324972	snp	C/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67916568	GCACTCCAGCCTGAG[C/G]GACAAGAGCAAAACT	2186
rs553334786	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67977822	GCACTCCAGCTTGGG[C/T]GACAGAGGGAGATTC	2186
rs553419502	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67857562	GCCTCGACCTCCTGG[C/G]CTCAAGCAGTCCTCC	2186
rs553424788	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67828779	TTGATCCACCTGCCT[C/T]AGCCTCCCAAAGTGC	2186
rs553426353	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67958675	TGGGGAGGTTGGAGT[A/G]CGCTGAGATTGTGCC	2186
rs553436870	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67970599	ATGTGTTTAGAAATG[A/C]ATAGAAAATGTCTGG	2186
rs553457142	snp	A/T	0.00438332	0.0466095	intron-variant	BPTF	GRCh38.p7	17:67909462	TCTTTTTTTTTTTTT[A/T]AAATGAAAAAATGAA	2186
rs553460206	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67901076	CCAAAAGGGGAAAAA[A/G]TAGATGTTAGTGAAA	2186
rs553477006	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67884551	CCCTCAAGTACGTAG[A/G]ACTAGAGGCATGCAC	2186
rs553480008	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67843943	GCTAATTTATTATTA[G/T]TAGTAGAGATGGGGT	2186
rs553481030	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	BPTF	GRCh38.p7	17:67983313	GTCCATTGTCATCAC[G/T]TCAGAGAAAAATCTT	2186
rs553489999	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67899857	CAAAAGGCAAACTTA[C/T]ACAGTTTGGGATGCA	2186
rs553522648	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67951792	CAGGTGCAGTGGTTC[A/G]TGCCTGTAATCCCAG	2186
rs553544929	snp	A/G	0	0	intron-variant	BPTF	GRCh38.p7	17:67858484	CGCTTGAACCTAGGA[A/G]GCGGAGGTTGCAATG	2186
rs553583773	snp	A/G	0.000193269	0.00982839	intron-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67929539	TGAGCACATCACATT[A/G]TTTTTAGAATGACTT	2186
rs553610774	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67916266	GGCTAGAGCTTTCTC[A/T]TTCACAGTGTTCATT	2186
rs553615052	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67851157	AAGCTTCGGCAGAGT[C/T]TGGGACCCTAGCTCT	2186
rs553615736	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67862945	TATCAAGCACCTAAC[A/G]GTTCTTCAGCCTCTT	2186
rs553628415	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67863296	TTTTCTTTTTCTTTT[C/T]ATTTTTTTGAGACAC	2186
rs553643648	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67838316	TAGGAAAAAGGCTTT[G/T]AGTTTTACAAATAAT	2186
rs553656232	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67837741	AACTTTTTCTAGAAT[C/T]TACTAAGGTTTACTC	2186
rs553676254	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67872300	TTTTCAACCAATTTA[A/G]ATGGTCTAAACTTAG	2186
rs553683457	snp	C/T	0.00835141	0.0640778	intron-variant	BPTF	GRCh38.p7	17:67859545	AGACCCTGTGGCTCT[C/T]AGGAGGTAGAACCTG	2186
rs553689719	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67864196	AATAATTTTGATTAT[A/C]TAAACTGTATATAGG	2186
rs553731169	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67860185	TTTTCTATGTAAAAT[C/G]AAGTAGGAAACTTTA	2186
rs553758735	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67871123	TTATCTACACACACA[C/T]GTGTCTACTTTAGGA	2186
rs553786792	in-del	-/A	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67871527	TGTAACTAAATATAC[-/A]AGCTTACTATATTTG	2186
rs553798110	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67829021	CTTGTAATAGATGAA[A/G]TTTTGATAACTCTAC	2186
rs553802458	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67835721	CCCAGGCTGGAGTGC[A/G]GTGGCGCGATTTCGG	2186
rs553808100	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67853809	GAATCATTGCTTCTT[C/T]GTATTATTTTAACTT	2186
rs553834808	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67963527	TTCTGATAAGAGCAT[C/T]ATATTTAATAATTTA	2186
rs553895852	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67968519	TGCGGTGGCTCACGC[C/T]TGTAATACCAGCACT	2186
rs553897198	in-del	-/A			intron-variant	BPTF	GRCh38.p7	17:67922031	CAAGACTCTGTCTCC[-/A]AAAAAAAAAACAAAA	2186
rs553907364	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67936426	ACTTAGAAAACTGAC[A/G]GTTGTGGTAAATTGC	2186
rs553914179	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67940805	GCAGAAATACCTCTT[A/G]GACAGGATATAATAA	2186
rs553929895	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67842490	TCTTAGACCTCTCCT[C/T]TAAACTCCAGTTATG	2186
rs553930179	snp	A/G	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67921063	CATACAAAAATTACA[A/G]AAATATTGGTAATGT	2186
rs553998676	in-del	-/TGC	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67833461	GGCCATTAGGAATAA[-/TGC]TGCTGAGCACATTCG	2186
rs554044166	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67949566	GACAACAGAGTGAGA[C/T]TCCATCTCAAAAAAA	2186
rs554061041	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67849489	TTTCATGACATTCAA[G/T]GAATAGCAAGGTTTG	2186
rs554074551	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67907144	GAGCTGAGATGAACC[C/G]ACTGTGCTCCAGCCT	2186
rs554086413	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67877938	TGCACCCAGCAACTT[A/T]AAAAAATTGAAATAT	2186
rs554090723	snp	C/T			intron-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67918859	GGGGAAGGGAGTTAT[C/T]TTCTAATTTAAGTTT	2186
rs554117169	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67926477	CTATAGGCGCCCGCC[A/C]CCACGCCTGGCTAAT	2186
rs554136030	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67906619	TCTTACCTCACCACT[A/G]TCCTGCTCTTGACAG	2186
rs554188324	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67866242	CACAAAGTACTCTCA[C/T]GTGGTTCTGAATTTT	2186
rs554202444	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67844016	GTGATCCACCCACCT[C/T]AGCCTCCCAAAGTGC	2186
rs554206715	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67977510	TCAGAGTGAGACTCC[A/C]TCTCAGAAGAAAAAA	2186
rs554208602	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67970760	CTTAATACTTTTTCA[C/T]ATCAGCTGTTATAGA	2186
rs554212555	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67860922	TATGCTTTTAAATCT[A/G]TACAGCTTTCTACTC	2186
rs554226234	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67887214	ATTCTTACTCATGTG[G/T]TTAAGTTTCTTACAT	2186
rs554258799	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67913275	TTTAAAAAATGAGAT[A/G]ATAGAGATAAGACAG	2186
rs554280540	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67953055	AAGCTCCGTCTCCCC[A/G]GGTTCACGCCAGTCT	2186
rs554294460	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67958460	GGGCCAGGCAGTGTG[C/G]CTCACACCTGTAATC	2186
rs554333602	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67841981	TTGCTGTAGGAATTA[C/T]AAAATATATACCTAA	2186
rs554338980	snp	C/T	0.00119737	0.0244387	intron-variant, utr-variant-5-prime	BPTF	GRCh38.p7	17:67889739	CTTGAACCCAGGAGG[C/T]AGAGGTTGCAGTGAG	2186
rs554342181	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67897330	TAGGCAACAAGAGTG[A/T]AACTCTGTCTCAAAA	2186
rs554343942	in-del	-/GAC	0.00450448	0.0472435	cds-indel, nc-transcript-variant	BPTF	GRCh38.p7	17:67826265	CCGGAGGAGATGGAA[-/GAC]GACGACGACGACGCC	2186
rs554347962	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67839547	ACTGTTTGACTTTTA[A/G]AAAGGTATTTTAATT	2186
rs554357803	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67958098	ACACTTTGGAAGGCC[A/G]AGGCAGGTCACTTGA	2186
rs554372112	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67885384	AGGTCAGGAGTTCGA[A/G]CCCAGCCTGGCCAAC	2186
rs554399514	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67867264	CTTTAATTCAAGTAT[A/C]TTATTAAACTTTTTT	2186
rs554399647	snp	A/G	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67896169	GGGTTTCACCGTGTT[A/G]GCCAGGATGGTCTCC	2186
rs554411710	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67869950	GAGCTTGCAGTGAGC[C/T]GAGTGAGCCACTGCA	2186
rs554412736	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67838827	AGTATAATTCATTTG[C/G]TAAATATTTTCACTT	2186
rs554433563	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67952613	GAACGTACAGTTCCC[A/G]TATTATTCCTCCCCC	2186
rs554474786	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67848631	ATTAACAGATTATGA[C/T]TACAGTGCGTATTTA	2186
rs554519425	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67928239	GAAGTAAAATACTTC[A/G]GAAATGTAGTGGAAT	2186
rs554536543	in-del	-/TT			intron-variant	BPTF	GRCh38.p7	17:67894271	GGCCATATTGAAGAC[-/TT]TACTTTTGGCCTCAT	2186
rs554542783	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67890864	TTCATTTGCCAGTGC[C/T]ACAGTGTCTTCATTT	2186
rs554600280	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67857628	TGTGCTACCATGCCC[A/G]GCTAATTTTTGCATT	2186
rs554658427	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67921932	AGCTACTCGGGAGGC[C/T]GAGGCACGAGAATTG	2186
rs554660880	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67937340	TTGGTGCCTGTAATC[C/G]CAGCTACTCGGGAGG	2186
rs554717626	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67934700	AACATGGTGAAACCC[C/T]GCCTGTACTAAAAAT	2186
rs554718708	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67915029	AAAGCATATTGCTAT[A/G]AAAAGCCATGCACGT	2186
rs554742854	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67964749	CTCATGCCTGTAATC[C/T]CAGCACTTTGGGAGG	2186
rs554744467	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67858139	GAGGGAACAAAATGA[A/T]ATCTGTCACCTTAAC	2186
rs554746335	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67899158	ACACCACCTATAAAA[C/T]TGCTGAAGCAATAAT	2186
rs554802548	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67969698	AATACCAAGATAAGC[C/G]CCAAATGGTGGTTCC	2186
rs554839232	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67942445	ACCATATGCTTAAGA[C/G]ATTGGTACAAATTTA	2186
rs554847368	snp	C/T	0.0799831	0.183287	intron-variant	BPTF	GRCh38.p7	17:67843201	ACATACATCTACATA[C/T]ATGTAGATGTATGTA	2186
rs554854399	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67935421	TGACAGAGTGAAACC[C/G]TGTCTCAAAAAAAGA	2186
rs554856342	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67902476	CTCCTTAGTTCCAAG[C/T]GTGTTGGCAGAGGGA	2186
rs554877324	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67907819	ACTCAACAAATTAAC[C/T]GTAATTAACAAATTA	2186
rs554886054	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67885583	CAACAGAGTGAGACT[C/T]CATCTTAAAAAGAAG	2186
rs554932830	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67899953	AGGGAGTTGGACACA[A/C]AAGCATCTGATGTAT	2186
rs555004146	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67892556	TGTGCTTCAGCTAGC[C/T]GTGGTGACAGGACAT	2186
rs555007946	snp	C/T	0.000138624	0.00832423	intron-variant	BPTF	GRCh38.p7	17:67975995	TCTGAATTAATTCAA[C/T]TCTTCACACTCTTTA	2186
rs555014646	snp	A/C/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67949280	TAAGGCAGGATGATC[A/C/G]CTTGAACCCGGAAAG	2186
rs555063951	snp	C/T	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67905899	CACACCGGGGCCTGT[C/T]GTGGGGTTGGGGGAG	2186
rs555066800	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67914166	CCGTTTTCATTTCCC[C/T]TTAGGCTTCGTTTTT	2186
rs555181113	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67941588	GTGGACACTTGTTAT[A/G]TGACAAAGGTGACAT	2186
rs555199607	snp	C/T	0.00358779	0.0422022	intron-variant	BPTF	GRCh38.p7	17:67861465	GGGATTACGGGCGGC[C/T]GCCACCACACCTGGC	2186
rs555204974	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67938776	GCATTTTTTAAAATT[A/G]CAAGTTTAGAAATAA	2186
rs555207085	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67863153	ATCATGGGTCAGCAG[A/G]GTTGGTTTTTCTGGA	2186
rs555228831	snp	C/G	0.00478085	0.0486577	intron-variant	BPTF	GRCh38.p7	17:67883692	GCAACCTCCGCCCCC[C/G]TGGGTTCAAGCAGTT	2186
rs555249817	snp	A/G	3.29533e-05	0.00405901	missense, nc-transcript-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67918833	GAGGAGGGACTACAC[A/G]GACAGGTAAGGGGGA	2186
rs555261244	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67849575	TAGGGAAAATAACCT[A/T]TCAGGATATAGGGAG	2186
rs555265183	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67975435	ATACACTAAATGGTT[G/T]GCATGTAAAAATGCA	2186
rs555269449	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67936546	ACATGCATAAGTGAA[C/T]GTGTAGTTTCCAAAC	2186
rs555289218	snp	A/G			missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912287	GGCCATTCATTAATG[A/G]TGATGTCATCATGGA	2186
rs555290711	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67876795	TGGGCGACAGAGCAA[G/T]ACTTCATCTTAAAAA	2186
rs555322614	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67850470	GTCTCCTGGGTTCAA[A/G]CGGTTCTTCTGCCTC	2186
rs555324894	snp	C/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67919931	TTATTCCACGTGTGT[C/G]TCTTTTTGAAAGCAC	2186
rs555352978	snp	A/G	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67956520	ATGGTGTTTCGCCAC[A/G]TTGGCCAGGCTCGTC	2186
rs555358733	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67907862	TCAGTCCATATTCCA[C/T]TTGCCCTGGTTGTCT	2186
rs555364356	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67883053	GGGCTTGGTGGCTCA[C/T]GCCTATAATCCCAGC	2186
rs555398225	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67856587	TGACTTAACCATTGG[A/G]TGATTTTCATTGTCT	2186
rs555399430	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67846731	TTGTTTGGAGACAGG[A/G]TCCCTGTCGCCTAGG	2186
rs555407551	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67855098	CTGAGGTTGAGAGTT[C/T]GAGACCAGCCTGGCC	2186
rs555409613	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67980672	TGGAGGTCCTGGGGA[C/T]TGTAGGCAAGACAAA	2186
rs555414097	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67862560	GCTCCAGAATGTGTG[C/T]TCCTAAGCACTACTT	2186
rs555416789	snp	A/G	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67963033	CATTCATTCAGAGGA[A/G]GACATTACCATCAAT	2186
rs555418388	snp	A/C	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67955898	ATGGCCTGTAATCCA[A/C]GCACTCTAGAAGGCT	2186
rs555428576	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67949698	ACATACATATATATA[C/T]ACACACATGTATATA	2186
rs555491852	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67954516	ACAGCATGTTAGTCT[C/T]CCTTACCCCCCAGAA	2186
rs555501717	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67961375	TTCTAAGGAGTGTTT[C/T]GTAATCTCTTGTCCC	2186
rs555515147	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67939383	AGAAATTTGATGTTA[C/T]TCAGTAGTTAGTAAT	2186
rs555532791	snp	G/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67856094	TTTATCTTGAGCTAT[G/T]ATTTTATTGAACGTT	2186
rs555542396	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67974098	CTAAAATATTCACTA[A/G]CCTTTAGTTTGAAAT	2186
rs555547891	snp	C/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67973561	CAAGCAGTGGTGAGT[C/G]CAGTGGTGCGATCTT	2186
rs555556175	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67890649	CAGAATCATATGATT[A/G]AAGTGTGGGAGGGCG	2186
rs555583714	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67827494	CAAAGCAACAACCGG[C/G]AAGACTTTTCCTTTA	2186
rs555591326	snp	A/T	8.40343e-05	0.00648152	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67912246	GAATGATATTAAATC[A/T]TTGACTGTTAAAGAA	2186
rs555593187	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67834530	TATTGTGAAGGATTT[G/T]TCTGTTTCTCCTTGA	2186
rs555593974	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67884168	TTTTTGAAACAATCT[C/T]GTGCTGTCACTCAGG	2186
rs555638725	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67933871	TGAGACCAGCCTGGC[C/G]AACATGGTGAAACCC	2186
rs555684576	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67861608	GATGTGAGCCACCAT[A/G]CCCAGCCATAGCTGG	2186
rs555696137	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67939857	CGCACTCCAGCCTGG[A/G]CGACAGAGCGAGACT	2186
rs555728504	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67881996	CCCACAACCACACCC[A/G]GCTAATTTTTGTATT	2186
rs555738061	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67898326	AGATCGCACCAGTGC[A/C]CTCCATCCTGAGCAA	2186
rs555777576	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67832693	CCCGCAAAAGAAGCC[C/T]GCACCGTCAGCATCA	2186
rs555800462	snp	A/G	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67829665	TTTTAGAACTGGTTT[A/G]AGATATCCGAATAAC	2186
rs555811669	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67892591	CCAACTTTGTCTCCC[A/G]TATTCGAGAATTATT	2186
rs555811751	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67863991	TCTCTTTGCCACCCT[A/G]TGAGTCCTTGAGAAT	2186
rs555848928	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67874140	AACCCAAAGAATATA[A/G]TTAATATCCATGAGT	2186
rs555872887	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67944955	TCCCAGTTTCAGAGC[A/G]TCCTGCCCTAAGCGT	2186
rs555873076	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67899257	AAAGATCCAAAAGCA[A/G]GAAGTACAGAGCCAG	2186
rs555875033	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67908368	TTCACCTTGTTGGGC[C/T]GGTGTTGAACTCCTG	2186
rs555882013	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67906560	CACATATGCACAGAG[A/T]GATAGAACGCTGGCA	2186
rs555884336	snp	A/G	0.00795532	0.062565	intron-variant	BPTF	GRCh38.p7	17:67850558	ATTTTTCTTAGAGAC[A/G]GGGTTTCACCATATT	2186
rs555904479	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67957165	GCACATGCCTGTAAT[C/G]CCAGCTACTCAGGAG	2186
rs555935989	snp	G/T			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67887557	ACTTCTATAACTTTG[G/T]TTTCAACCTATCTGA	2186
rs555939488	in-del	-/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67872494	GTGGATCACCTGAGG[-/T]CAGGAGTTTGAGACC	2186
rs555961042	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67968377	TTAATCATTGTACAT[A/G]TTTCAAATTTGGGTA	2186
rs555999182	snp	A/G	0.0023933	0.0345097	intron-variant	BPTF	GRCh38.p7	17:67868278	CTTTCTCCAGAGGCA[A/G]TCATTATTGCTGTAT	2186
rs556018059	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67869914	GCCTGAGGCAAGAGA[A/G]TGGCGTGAACCCGGG	2186
rs556059563	snp	G/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67904060	TTGAGACAGAGTCTC[G/T]CTCTGTTGCCCAGAT	2186
rs556070265	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67859478	GTCTGCATCTTATAG[A/G]TAAAGAGACTAAATC	2186
rs556143004	in-del	-/A			intron-variant	BPTF	GRCh38.p7	17:67977519	ACTCCATCTCAGAAG[-/A]AAAAAAAAAAAGTGT	2186
rs556158157	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67886479	ATGTTCTTTTCCTTT[A/C]TTTTTCATTTTTTTT	2186
rs556164204	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67877835	ACAAGGTCTCACTGT[A/G]TTGCCCAGGCCAGTC	2186
rs556186769	snp	G/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67828282	AATCACATGTTGGTC[G/T]TCTTTGCACCCAGAG	2186
rs556189642	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67856719	CTTGAAGCATGAAGG[C/T]CTTGCTGGTGGTATT	2186
rs556198039	snp	A/C	0.000798403	0.0199641	utr-variant-3-prime	BPTF	GRCh38.p7	17:67982563	ATTGAAAAAAAAAGA[A/C]AAAGAAAGCAAGAAA	2186
rs556222127	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67967890	TCAGATGGTGTCTGA[A/G]TGGAGTATTATGCAG	2186
rs556227008	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67949786	TTCAAGGCCAGACAC[A/G]GTGTCTCACGCCTGT	2186
rs556265544	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67855529	GGTTGGAATCCCCCA[A/G]GAGAAGATGATCCCA	2186
rs556282361	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67963151	TTTATGTTTCCACAT[A/G]TGATAGAGCATCAGA	2186
rs556287261	snp	A/C	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67974300	ACAGCAAAAAAAAAA[A/C]CAAACTTGTTTTCCT	2186
rs556291638	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67955699	AGACATGGTGGCGGG[C/T]GCATGTAATCCCAGC	2186
rs556305120	snp	G/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67952997	ATAGAGTCTTGCTCT[G/T]TCGCCCAGGCTGGAG	2186
rs556336245	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67847653	GCACTCCAGCCTGGG[C/T]GACAGAGCCAGACTC	2186
rs556357020	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67955079	CGGATCACGAGGTCA[A/G]GAGATTGAGACTATC	2186
rs556375365	snp	A/G/T	4.94368e-05	0.00497152	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67920084	GTCCTTATGGCATTC[A/G/T]ATCTGAATATTGTAT	2186
rs556383650	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67859537	TTTGCCCAAGACCCT[A/G]TGGCTCTTAGGAGGT	2186
rs556384542	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67906115	TGAAATGGAGTCTTG[C/T]TCTGTCACCAGGCTG	2186
rs556390982	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67934613	GGGTGTGGTGGCTCA[C/G]TCCTGTAATCCCAGC	2186
rs556417372	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67956701	AGGCACAGTGGCTTA[C/T]GCCTGTAATCACAGC	2186
rs556429541	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	BPTF	GRCh38.p7	17:67981523	TACCTCGTGATTACC[C/T]AATTCAAAATTGCCC	2186
rs556431769	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67949158	ATTGTTTGAGCCCAG[A/G]AGTTCAAGATCAGCC	2186
rs556442528	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67919402	AAAAGAAAAAAATCA[A/G]CTAGGCCTTGTGTTT	2186
rs556442571	snp	C/T	0.00557542	0.0525036	intron-variant	BPTF	GRCh38.p7	17:67926441	GCCATTCTCCTGCCT[C/T]AGCCTCCCGAGTAAC	2186
rs556445868	snp	G/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67913248	AGAATTATCTCACAA[G/T]AATATCTCATTTTTA	2186
rs556476375	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67883756	CAGGCGCCTGCCGCT[C/G]TGCCCAGCTAATTTT	2186
rs556479770	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67855870	CAGTGTGCTGTCGAG[A/G]GGTCTGAATCCACAC	2186
rs556492823	snp	A/G	0.00993419	0.0697739	intron-variant	BPTF	GRCh38.p7	17:67933954	GAGGCTGAGGCAAGA[A/G]AATTGCTCGAACTCA	2186
rs556548410	snp	C/G/T			intron-variant	BPTF	GRCh38.p7	17:67828726	AATGACGGGGTTTCT[C/G/T]CGTGTTGGTCAGGCT	2186
rs556551008	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67951145	GCTTCATTACATAGT[C/T]ATTAATGATTACATC	2186
rs556574064	snp	G/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67940196	GAAGAATTTTAATTG[G/T]TTTTTTCCATTATCC	2186
rs556603779	snp	C/T	0.00358779	0.0422022	intron-variant	BPTF	GRCh38.p7	17:67890746	ACAAAATTGTCTTAA[C/T]TATTTTCCCCAAAAT	2186
rs556612871	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67905041	GATGTCTCAGATTTC[C/T]GTAAGATTGTAGAAT	2186
rs556620007	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67844473	AGTATGGTCTCGATC[G/T]CCTGACCTCGTGATC	2186
rs556686032	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67966779	AATTGGTATGGTCAC[C/T]TTGGAGGGTAAATTG	2186
rs556711422	snp	C/T	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67904173	AGCTGGGATTATAGG[C/T]GTGCACCACCACGCC	2186
rs556727867	snp	A/C/T			intron-variant	BPTF	GRCh38.p7	17:67864253	CTTTTCAGCCCGGTG[A/C/T]GGTGGCTCGTGCCTG	2186
rs556798462	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67910661	AAAAATAAGCCAGGC[A/G]TGGTGGCACATGCCT	2186
rs556852274	snp	A/G	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67855251	GGCTGCAGTGAGCTG[A/G]GATCACACCACTGCA	2186
rs556867085	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67890073	TTTGTAGAAATTTCT[A/G]GACCTACTTTTGAAT	2186
rs556884100	snp	A/G	0.00318978	0.0398085	intron-variant, utr-variant-5-prime	BPTF	GRCh38.p7	17:67888926	GGGGTTTTTTCTGAC[A/G]GTAGCACTCACTTGT	2186
rs556888276	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67876375	CATTTGAGTACTGGT[C/G]AGCAGTGAGCTGTGT	2186
rs556910779	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67938440	GAAAAATTTAGAAGA[A/C]AGAGTAATAATGGAA	2186
rs556921278	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67850826	TTGATTGTTTCTTTG[C/T]TTTTATAAACATATT	2186
rs556954982	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67961847	GATGTGGTGGCACAC[A/T]CCTGTAATCCCAGCT	2186
rs556997940	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67961390	CGTAATCTCTTGTCC[C/G]AAACTAGGCTGGTTT	2186
rs557005117	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67867129	TTACTTTAGTTCTCC[A/G]TATTTCATTTTCCCA	2186
rs557005292	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67896055	TGCAGCTCCGCCTCC[C/T]GGGTTCACGCCATTC	2186
rs557005607	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67868966	TATTAGATCTGTTTA[C/G]AAAAATGTGTAATTT	2186
rs557024472	snp	G/T	0.000399281	0.0141238	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67826096	GGCCGTCAACAAAGT[G/T]GTGTACGATGACCAC	2186
rs557026311	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67956060	GCAGTGGCTCACGCT[G/T]GTAATCCCAGCACTT	2186
rs557066518	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67902682	GGGACACAAAGCCGT[C/T]GTAAAAGTTGGGAGG	2186
rs557091526	in-del	-/ATT	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67952695	AATGAGCCAATAGTG[-/ATT]ATTATTATTATTATT	2186
rs557134103	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67971195	GCAATTCTCCTGCCT[C/T]AGCCTTCTGAGTATC	2186
rs557136842	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67875946	TGAAACTCATCATAA[A/T]TTTCATGCTTCTTAA	2186
rs557175680	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67840254	GGATTTCAAGTGCGC[A/C]CCTCCACAGTTGGCT	2186
rs557187070	snp	C/G	0.000754432	0.0194074	upstream-variant-2KB	BPTF	GRCh38.p7	17:67825491	GGGCCTGCGGCCGCT[C/G]TCGGTTCCCCCAGTC	2186
rs557205497	snp	C/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67868614	AGATAAAATTATTAG[C/G]TAAGATTCTGAAAGT	2186
rs557231812	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67932075	CCAGTCTAGGAAATA[C/T]GTAATTCTCTGCATT	2186
rs557253244	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67845749	CTGCACTCTAGCCTG[A/G]GCGACAGCAAGATTC	2186
rs557257375	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67972553	CTGGCTATTTAAGGG[C/T]TATTTATATACTAAA	2186
rs557266289	snp	C/T	0.00199481	0.0315187	intron-variant, utr-variant-5-prime	BPTF	GRCh38.p7	17:67889545	AGGCGCAGTGGCTCA[C/T]GCCTGTAATCCCAGC	2186
rs557275249	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67873330	GGGTGTGGTGGCAGG[C/T]GCCTGTAATCCCAGC	2186
rs557312497	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67846425	TGTCCAATAGAACTT[C/T]TTGTGATGATGGAAA	2186
rs557314640	snp	A/G	0.0023933	0.0345097	intron-variant	BPTF	GRCh38.p7	17:67839504	TACATTCCTGCAGCA[A/G]ACCTCTCTTGATCCT	2186
rs557318737	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67979241	AAATATTTACATTTT[C/T]GTAGTAACGTAAATA	2186
rs557321929	snp	C/T	1.65436e-05	0.00287602	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911396	TGTTAGATGATGTCT[C/T]CATTCGGAGCCCAGA	2186
rs557343386	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67960025	CTTGCATGTGATATT[C/G]TTACCATTGACGCTA	2186
rs557347047	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67953797	GTTTGCCAGGCTTGT[C/G]TCGAACTCCTGACCT	2186
rs557352170	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67959249	CCAGATGGGACAGGG[A/G]CAAGCCAGGAGGGAC	2186
rs557397269	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67878709	GTGTGTGTGTCAGTC[A/G]TTTAGATATCCTCTT	2186
rs557407801	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67953299	TCTTACTCTGTCACC[C/G]AGGCTGGACTGCAAT	2186
rs557411134	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67965438	TGTGGTTGCTCACAC[C/T]TATAATCCCAGCACT	2186
rs557419233	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67934225	AAGATGTGTTAGGAA[A/G]TAAAAGACATGACCG	2186
rs557427998	snp	C/G	0.0103295	0.0711199	utr-variant-3-prime	BPTF	GRCh38.p7	17:67983754	ATTAGCTTTGTCCTA[C/G]CAACTTCTGGAATTT	2186
rs557429346	snp	A/G	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67955162	CAGGCATGGTGGTGG[A/G]CGCTACTTGGGAGGC	2186
rs557466540	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67859965	TTTTGATACATTGTC[G/T]AGGAAATCAAATATT	2186
rs557487318	snp	A/G	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67970279	TGGTGCCTCATGCCT[A/G]TGGTCCCAGCCCGAG	2186
rs557573231	snp	G/T	0.000181068	0.0095132	intron-variant	BPTF	GRCh38.p7	17:67922789	AGATGCCAGAAGTAC[G/T]TTAATTTTAGAAGCA	2186
rs557594688	snp	A/C	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67904260	TCTTGGAACTCCTGA[A/C]CTCAGGTGATCCTCC	2186
rs557606707	snp	C/G	0.00398564	0.0444627	intron-variant	BPTF	GRCh38.p7	17:67869750	GCATTTTGGGAGGCT[C/G]AGGCGGGCGGATCAC	2186
rs557610963	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67964811	CAGACCATCCTGGCT[A/G]ACACGGTGAAACCCC	2186
rs557617409	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67880608	ATATTCAAACATTTG[G/T]AGGTTTTTGTTTTTG	2186
rs557620529	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67882421	TAGCATACTTAGTTT[C/G]TTTGTTTACATTTGT	2186
rs557636479	snp	C/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67922477	AATTCATGTTGGGGT[C/G]CAGAGGATGAATTGA	2186
rs557638168	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67930516	GATATGTAATTTCTT[G/T]GTTACTAGTATGGAA	2186
rs557639740	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67831251	TAGAGAGAGGAATGC[A/G]TTACATATGCCTCCC	2186
rs557669526	in-del	-/TAAA	0.00279162	0.0372561	intron-variant	BPTF	GRCh38.p7	17:67921529	GACTCCATTTCCAAG[-/TAAA]TAAATAAATAAATAA	2186
rs557676111	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67972684	CTTGGAGTCTTTTTC[C/T]TCCTCCATAATATAT	2186
rs557691121	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67966411	GTAGAGGAAGCTCAT[C/G]TTAGGTAACTATTAC	2186
rs557747967	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67938027	CTGAGGCAGGAGAAT[C/T]GCTTGAACCCAGGAG	2186
rs557787520	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67862438	GGATATGTACCGTCA[C/T]CCTATTTTTCAGATG	2186
rs557804241	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	BPTF	GRCh38.p7	17:67889620	CAAGACCAGCCTGAC[C/T]AACATGGTGAAACCC	2186
rs557866903	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67896077	ACGCCATTCTCCTGC[C/T]TCAGCCTCCCGAGTA	2186
rs557933404	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67853746	TGGTTTATAATCTAA[A/T]GGGAAAACTTTGCAT	2186
rs557938511	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67979791	CATGCCTGTAATCCC[A/G]GCCCTTTGGAAGGCC	2186
rs557946676	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67876022	ATCACCAGACCATAG[C/T]GGCAGATATTTTGGT	2186
rs557947978	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67913312	TATTAATGGCCAAAG[A/G]TAGTAATGGAAACAG	2186
rs557959487	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67834434	TGTCAATTAGGTCAA[A/G]TTTGTTGATAATGTT	2186
rs557981504	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67826633	GTGCCAGTGCAGTGT[C/T]TCCACCGGGCAGGAT	2186
rs557998478	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67845850	AAAAAAGAAAAACAG[G/T]GGATCTTTATGTTAC	2186
rs558027110	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67939830	GGTTGCAGTGAGCCA[A/C]GATCACGCCACCGCA	2186
rs558035327	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67840331	AGACTGATTTCAAAC[C/T]CCTGGGCTCAAGCAA	2186
rs558049112	snp	G/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67925061	TCCAGGTTTTTTTTT[G/T]TTTTTTTTTTTTAAG	2186
rs558077845	snp	C/T	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67973258	AGATGCCTGTAGTCC[C/T]AGCTACTCCAGAGGC	2186
rs558096753	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67840966	CTGTCAGTGCCTTGC[A/G]TTTCATTCTCTTAAC	2186
rs558098638	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67833314	AAACTCCTGGACTCA[A/G]GCAATCTTCCTGCCT	2186
rs558120678	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67846483	GTAGCCACGAGACAC[A/G]TGGCTATTAAGTAAG	2186
rs558128312	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67902782	CCTCCCACATCTTTT[C/T]GGCATCACTACCCCA	2186
rs558131099	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67918654	GTAGAGTGAATATGA[A/T]TGTGTATGTGTATGT	2186
rs558134723	in-del	-/TGAA			intron-variant	BPTF	GRCh38.p7	17:67893273	TATCTTAACTTACTT[-/TGAA]TGATTAATTTTAATT	2186
rs558134930	in-del	-/AT	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67973387	AGAAAAAAAAATAAA[-/AT]ATATATATATAACAA	2186
rs558142754	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67970776	ATCAGCTGTTATAGA[C/T]CTACATCATTTTAAA	2186
rs558165893	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67954437	TTTTCTCTCCCAAAG[C/T]CCAGTGGAGCCCAGT	2186
rs558173070	snp	A/G	0.00636936	0.0560724	intron-variant	BPTF	GRCh38.p7	17:67937372	TGAGGCAGGAGAATC[A/G]GACTTTGTCAAAAAA	2186
rs558211921	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67965541	CATCTCTACAAAAAA[A/T]TTTTTTAAAAATCAG	2186
rs558217173	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67946449	ATGTTTAAATTTAGA[A/G]GAAACACTGAATTGA	2186
rs558244245	snp	A/C	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67839043	GCAAAAATGAATCAT[A/C]TGTACACATCTGATT	2186
rs558247177	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67930716	TGGGAGGCTGAGGCG[A/G]GAGGATCACTTGAGG	2186
rs558253365	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67839351	AAAAAAAAATCAGCT[A/G]TGGCTATTGTATTTT	2186
rs558255221	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67831503	TTTCTATTCTGCTCA[C/T]CCACGGGCGTGTTTG	2186
rs558265529	snp	C/T			intron-variant, utr-variant-5-prime	BPTF	GRCh38.p7	17:67889756	GAGGTTGCAGTGAGC[C/T]GAGATCGCACCACTG	2186
rs558268093	snp	G/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67896226	CTTGGCCTCCCAAAG[G/T]GCTGGGATTACAGGC	2186
rs558275575	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67977623	CCGAGGCGGGCGGAT[C/T]ACGAGGTCAGGAGAT	2186
rs558281123	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67971277	AGAATCAGGGTTTCA[C/G]CATGTTGGCCAGGCT	2186
rs558288864	snp	G/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67939193	AATTTTACCATGGCG[G/T]TAGTTTAACAACAAC	2186
rs558299800	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67944039	GGTGACATTCAAATA[C/T]GTATTTTCATTATAT	2186
rs558308082	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	BPTF	GRCh38.p7	17:67824037	GGTTTCACCATATTG[C/G]CCAGGCTGGTCTCAA	2186
rs558317792	in-del	-/GT	0.237078	0.249666	intron-variant	BPTF	GRCh38.p7	17:67878684	TCTTTATGTGTTCGT[-/GT]GTGTGTGTGTGTGTG	2186
rs558344641	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67926198	TTTTTTGTAGAGATA[A/G]GACTTTTGCCATATT	2186
rs558367954	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67917065	GTACCTCCACACACA[A/G]TGTTTAGAAACAAAC	2186
rs558422078	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67958701	GTGCCACTGCACTCC[A/G]GCCTAGGCAACAAAG	2186
rs558466924	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67973736	GTCTCGGAACTCATG[A/G]CCTTGGATGATACGC	2186
rs558471102	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67900853	TGTCTCTACAAAAAA[A/G]TTAAAATTGGCCAGG	2186
rs558502116	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67952659	CCCCTATTAATGTTA[A/G]CATGGCACATTTGTT	2186
rs558511777	snp	A/G/T	0.00039443	0.014038	intron-variant	BPTF	GRCh38.p7	17:67909785	AGTCAGCTGTGGAGG[A/G/T]CAGCCTGGGGGTGAT	2186
rs558515036	snp	G/T	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67915217	CACCATCCATTCCCT[G/T]ATGCCCATCCTCCCA	2186
rs558522323	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67856229	TTTCCTTATCTTGGT[C/T]GTCCAACCCTGTTAT	2186
rs558538949	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67881629	CTGCCTTAGCCTCCC[A/G]AGTAGCCAGGACTAT	2186
rs558574832	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67844812	GCAATGGCATGATCT[C/T]GGCTCACCGCAACCT	2186
rs558586724	snp	A/G	0.00557542	0.0525036	intron-variant	BPTF	GRCh38.p7	17:67903658	CTACAACTAAGTTTT[A/G]TCAGTTGGGGTTGTC	2186
rs558653417	snp	A/C/G	0.0023933	0.0345097	intron-variant	BPTF	GRCh38.p7	17:67896242	GCTGGGATTACAGGC[A/C/G]TGAGTGACTGCACCC	2186
rs558655070	snp	A/G			intron-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67929637	AAAAAAATCTGTTAT[A/G]TTTCTGATAAGTGAA	2186
rs558667924	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67978251	CCAGCCTTGGCCTCC[C/T]AAAGTGCTGGGGCTG	2186
rs558706555	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67852768	GGAATTACAGGGTCA[A/G]AGGGACATACATTCA	2186
rs558743920	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67907871	ATTCCACTTGCCCTG[G/T]TTGTCTTAGAGATAC	2186
rs558845578	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	BPTF	GRCh38.p7	17:67984063	AAGTAGTTAAATATG[A/G]GTTATTTTGTCCTTT	2186
rs558867964	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67958187	ACAAAAATTAGCTGA[G/T]TTTGGTGGCACGTGC	2186
rs558894924	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	BPTF	GRCh38.p7	17:67983261	TTGTGCCTGGATTTC[C/T]CCAGGACAGCAGTGG	2186
rs558901157	snp	C/T	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67879251	GTTTCAAGCGATTCT[C/T]CTGCCTCAGCCTCCC	2186
rs558912829	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67857716	GAGCCATCTGCCCTT[C/T]TCGGCCTCTCAAAGT	2186
rs558919720	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67939431	ATTAGCTACCAAAAA[A/G]TTATTCTTAGCAACT	2186
rs558924070	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67958861	AATCCCAGCTACTTG[A/G]GAGGCTGAGGCAGGA	2186
rs558949057	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67844396	GGGACTACAGGCGCC[C/T]GCCACCACGCCTGGC	2186
rs558996690	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67865839	GCTCCTCTTCTCTCC[A/G]GTTTGGGCTTCGATT	2186
rs559041966	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	BPTF	GRCh38.p7	17:67824092	CCTCAGCCTCCCAAA[A/G]TGCTGGGATTACAGG	2186
rs559066301	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67858633	ATGCTGCCTGTCAGG[A/G]AGCCCGGTGCTTGTA	2186
rs559075379	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67872077	GGGATTCACCTGCCT[C/T]GGCCTCCTGAAGTGC	2186
rs559104442	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67957111	AACATGGAGAAACCC[C/T]GTCTCTACTAAAAAT	2186
rs559117023	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67830744	GAATAGGAAATAAAC[C/G]AAAGCTCCTTTGTAT	2186
rs559122561	in-del	-/GTTTTTTTTTTTTT			intron-variant	BPTF	GRCh38.p7	17:67881858	GGATTTTGGGTTTTT[-/GTTTTTTTTTTTTT]TTTTTTTTTTTTTGA	2186
rs559136611	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67865008	AGACCGGGTTTCACC[A/G]TGTTAACCGGGATGG	2186
rs559140253	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67870911	AGTAGCTGGGACTAC[A/G]GGCGCCCGCCACTAC	2186
rs559147750	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67936895	GTAATTTCCCAAGCT[A/G]TTAATCTGGGATTCA	2186
rs559161656	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67953382	TGCCTCAGCCTCCCA[A/T]GTAGCTGGGATTACA	2186
rs559182163	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67837658	CAGGCAATCTGCCCA[A/C]CTTGGCCTCTCAAAG	2186
rs559194876	snp	A/C	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67885729	TTGAAAAGTAAGACT[A/C]TAAGCTTCAGATTTT	2186
rs559227176	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67943091	TTATCATCAAAGTGA[A/G]GATAGTGCTTACCTC	2186
rs559255742	snp	C/T	0.0295035	0.117819	intron-variant	BPTF	GRCh38.p7	17:67843211	ACATACATGTAGATG[C/T]ATGTAGATATATACC	2186
rs559280201	snp	C/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67969820	AACAAAAAATGCTCA[C/G]GAGGCTGAGGCAGGA	2186
rs559316772	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67843826	GCTGGAATGCAATGG[C/T]GCAATCGTGGCTCAC	2186
rs559339711	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67923096	GATCTTGCTCTGTCA[A/C]CCAGGCTGGAGTGCA	2186
rs559342960	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67838022	TCACCTGTACAGTAT[A/G]GGATGGACTAGATGA	2186
rs559362088	snp	C/T	0.00835141	0.0640778	intron-variant	BPTF	GRCh38.p7	17:67922055	AACAAAATCACAAGG[C/T]CGTCCTGGCACAGAA	2186
rs559369322	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67908306	TGGGACTACAGGCTC[A/G]TACCACCATGACTGG	2186
rs559385731	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67873688	TGGTAAATGAACCCT[A/G]TACAGACACATAGGC	2186
rs559390418	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67922599	TCAGCAAACCACAGC[C/T]CATGAGCCTTGGCCT	2186
rs559420657	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67936559	AATGTGTAGTTTCCA[A/T]ACCACTCTCTTCTCC	2186
rs559425076	snp	A/C			synonymous-codon	BPTF	GRCh38.p7	17:67940647	ACTTACTCAGTTAAC[A/C]CAGGGCCACGTAAGT	2186
rs559446828	in-del	-/C			intron-variant	BPTF	GRCh38.p7	17:67954776	TTTCCCAAAATCCGT[-/C]CCCATGATGTTATAA	2186
rs559448660	snp	A/G	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67866843	ATGTGTCATTTGACA[A/G]TGTCATCATTGTATG	2186
rs559453168	snp	C/T			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67896403	AGGGTGGGAGGGGCA[C/T]AAGGGTTGTAAAAAT	2186
rs559475062	snp	C/T			utr-variant-3-prime	BPTF	GRCh38.p7	17:67982587	CAAGAAAAAAAGATA[C/T]TATGGGGTCAAGTGT	2186
rs559480308	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67964871	GGGCGTGGTGGCGGG[C/T]GCCTGTAGTCCTAGC	2186
rs559480441	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67900159	GCCCAGGCTAGAGGG[C/G]AGTGGCGCCATCTCG	2186
rs559482712	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67844184	TCCCAGGTTCAAGTG[A/C]GTCTCGTGCCACAGC	2186
rs559501049	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67952344	TCTCCGTTCACTGCA[A/T]CCTCTGCCTGCTGGG	2186
rs559516420	in-del	-/AAC	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67880102	ATTTATTAGCATAAT[-/AAC]ATCGTATCTTTTTTA	2186
rs559565742	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67971396	TTTTAGGCTTTTTTT[A/T]AAAAACAATGTCCAG	2186
rs559574048	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67907460	TCCCGGGTTCAATCA[A/G]TTCTCTTGCCTCAGC	2186
rs559620846	snp	A/T	0.00113669	0.0238129	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67894157	GCGAGAATCTTTAGG[A/T]CATACCAGGTAAATG	2186
rs559638515	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67906932	GTGCCATGGCTCACA[C/T]CTGTGATGGGATGCC	2186
rs559668614	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67962794	TTCATATCATATTTT[G/T]ACCATTTATCTTCTA	2186
rs559682300	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67879429	AGAGGCGTGAGCCAC[C/T]GCGCCCGGCTAGGGC	2186
rs559708134	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime	BPTF	GRCh38.p7	17:67982622	CCATGGAAATGCCAC[A/G]TCTGCTCTTCAGTGA	2186
rs559715813	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67898598	TACAGGTGTGAGCCG[C/T]TGCACTTGGCCTATT	2186
rs559740320	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67899176	CTGAAGCAATAATGC[A/G]GGTAGACAAATGGCA	2186
rs559748456	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67976415	GAGGCGGAGGTTGCA[A/G]TGAGCCAAGATCACA	2186
rs559750943	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67866095	CACTGCACTCTAGCC[C/T]GGGCGACAGAGTGAG	2186
rs559796848	snp	A/G	0.000449382	0.014983	missense	BPTF	GRCh38.p7	17:67944345	ACAGCCAGCACCACC[A/G]CCACCACTGTTTCCA	2186
rs559814541	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67884888	ATTTTCCCTTCGTGT[A/G]TTGTGAGACTTGGAT	2186
rs559839778	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	BPTF	GRCh38.p7	17:67984125	CACTGTGCTGATGCA[A/G]GAATTCTACATTTTA	2186
rs559899834	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	BPTF	GRCh38.p7	17:67983555	GTTTCTTCCACGTAA[A/G]GAAAAGTAGTGTAAA	2186
rs559903035	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67830107	TTTATGACATTGCCA[A/G]TATACTGAGAAGGAT	2186
rs559916636	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67934645	CATTGGGAGGCCGGC[A/G]GGTGGATCACAAGGT	2186
rs559920046	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67851371	CAAGGGGCTCACACA[A/G]CCTTTTCCAAGACTT	2186
rs559931664	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67881382	AAAGGCTCATGGTAT[A/G]TGGTTTTTGTACCTT	2186
rs559942093	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67845965	AAAGCTATTTTTATC[C/T]TTCAAAGGCTAAAAG	2186
rs559972005	snp	C/T	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	BPTF	GRCh38.p7	17:67982043	AATATTGGCTTTTTC[C/T]AGTGAGCTATTATGT	2186
rs559992438	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67927802	TATATGTGGTATAGA[A/G]ACATGAAAATACTGC	2186
rs559993927	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67856239	TTGGTCGTCCAACCC[C/T]GTTATCCAGTTTTTC	2186
rs560051406	snp	A/G	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67949956	TAGTTAGGAGTCTGA[A/G]GTGGGGAGAATTGCT	2186
rs560058396	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67856848	TGTTCACAACTGAGC[A/G]TGGTTTCTGCCAGTC	2186
rs560087388	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67974998	TGACTAGGTCTTTCC[A/G]GTGACCAGCCCCAAT	2186
rs560117078	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67961728	CCTGTAATCCCAACA[C/T]TTTGGGAGGCCGAGG	2186
rs560123596	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67968038	TACCCTCATTTCCCA[A/G]AAAAAAAAATGGTAA	2186
rs560127796	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67957770	TTGAGGTGGGAGGAT[C/G]ACTTGAGCCTGGCAG	2186
rs560129842	snp	C/T	0.0103295	0.0711199	intron-variant	BPTF	GRCh38.p7	17:67964782	AAGGTGGGCGGATCA[C/T]AAGGTCAGGAGATCA	2186
rs560155530	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67935701	TCTCTACTAAAAATG[C/T]AAAAATTAACTGGGA	2186
rs560196295	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67920597	TCAAAAAATGTTTAT[A/G]GAGCACCAGTACAAT	2186
rs560216054	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67934954	TGTAATTACAAAACA[A/G]TTCTCAAATAGCAGC	2186
rs560222396	snp	G/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67855668	AGGGCATCAGGCAGG[G/T]TTATAGTGTGGACTG	2186
rs560224320	in-del	-/TTTTTTTTTTTTTT	0.425432	0.178112	intron-variant	BPTF	GRCh38.p7	17:67925993	AACCTAACATATTAC[-/TTTTTTTTTTTTTT]TTTTTTTTTTTTTTT	2186
rs560235854	snp	A/T	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67827729	GAGAAGTAGGGTAGT[A/T]TTAAGCCAAATGTGA	2186
rs560240251	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67870011	CGTCTCAAAAAAAAA[A/G]AAAAAAAAAAAAAAA	2186
rs560260488	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67862228	TAATCCACCTGCCTC[A/G]GACTCCGAAAGTGCT	2186
rs560267204	snp	A/T	0.00636936	0.0560724	intron-variant	BPTF	GRCh38.p7	17:67919549	GTCTCTTAAAAAAAA[A/T]TTTTTTTTCACATAC	2186
rs560276888	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67933315	TAGCTAAAGCCTGTA[A/T]TCCCAAAACTTTGGG	2186
rs560319131	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67836284	CACACGCTTGGGAAA[C/T]GGCATGGCCATGTGA	2186
rs560372691	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67877186	CGGAGATGTATCAGT[A/G]ACCAAAATAGATAAG	2186
rs560376473	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67906247	CACCATGCCCAGCTA[A/G]TTTTTGTATTTTTTA	2186
rs560379913	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67967594	CGGAGGCCAAGGTGG[A/G]TGGATCACCTGAGGT	2186
rs560380006	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67840592	AGTTTCCTTCTTTCA[C/T]CCATGCTGGAGTGCA	2186
rs560409291	in-del	-/A	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67853198	TACATTTATATACTT[-/A]ACATATGTATATCTG	2186
rs560423780	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67917020	TTGAAATACGTTTTT[A/T]GTATTTTTTAAGAAT	2186
rs560438806	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67849201	AAAAATATAGATTAC[C/T]GAGCTTCACCTGGGG	2186
rs560443069	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67833871	CCGTGCCTGGAAGAA[A/G]GTAATTCAGGAGTTA	2186
rs560462920	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67941852	TAAATTCAACTACTT[C/T]AAAAATAAGAGTAAG	2186
rs560495082	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67890383	GTTTGCTGTTATCAA[C/T]GGTTTTCTCCATGTT	2186
rs560505280	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67879340	AGAGACGGGGTTTCA[C/T]CATGTTGGCCAGGCT	2186
rs560519370	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67974929	CTTAACCTTCAGCCC[C/T]TCTCCCCTTCCGGAG	2186
rs560551085	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67932606	CTTGGGAGGCCGAGG[C/T]GGAAGAATCGCTTGA	2186
rs560572034	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67872353	TGGTTTTATTTTCAT[C/T]AAATGGCACTGGGAA	2186
rs560572573	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67918950	GGCTGAGGCAGGTGG[A/G]TCATGAGGTCAGGAG	2186
rs560591062	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67847862	AGGTGAATCCTTGTT[A/G]CATTTGACAACTAAG	2186
rs560593852	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67826975	GAGTGCTAATGGGCC[C/T]GTGCAACAGTTGCTG	2186
rs560594996	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67974357	GAGAATTCTGTTTGG[A/C]GGCCTCTGGTCAGCA	2186
rs560625067	snp	G/T	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67970150	AGACAGGAGAATTGC[G/T]TGAACCTGGGAGGTG	2186
rs560644648	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67878796	TTTGTAGTTGTTTCA[A/T]GGGAGAGGGTAAATC	2186
rs560651636	snp	C/T	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67841236	AACATGGCGAAACCC[C/T]GTCTCTACTAAAAAT	2186
rs560729005	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67979997	AGATCGCACCACTAC[A/T]CTCTAGCCTGGGCAA	2186
rs560746937	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67843269	ATCTACATATATGGA[G/T]ACATATAGATATGTA	2186
rs560764752	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67951040	TCTCGAACTCCTGGC[C/T]TCAAGTAATCCACCC	2186
rs560768154	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67921054	CCTACAAAACATACA[A/G]AAATTACAAAAATAT	2186
rs560780250	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67837246	AGTGCTGTCCTGAAT[C/G]TGCTAGAGATGTACC	2186
rs560788423	snp	C/T	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67964800	GGTCAGGAGATCAGA[C/T]CATCCTGGCTAACAC	2186
rs560802864	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67975707	TACTTGTTAGAACTT[C/T]GGAGAATATTCACAT	2186
rs560810324	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67892156	TTTGAATTATATTTT[A/C]TCTGTTTCCGAAACT	2186
rs560823012	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67849882	GGTGACAGACGTTGC[A/T]GTGAGCTGAGATCGT	2186
rs560831072	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67978772	AAATGACTCATACAT[C/T]AGATAATTTGTTTAA	2186
rs560835844	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67829406	AGGTTTGTTGCATAG[A/G]TATACGTGTGCCATG	2186
rs560840794	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67925632	AGTTTTTACCAACTT[C/T]AGTATATAAACATTG	2186
rs560884279	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67842993	ATGTAAAAACACAAA[C/T]AGTTGTTTCTTAAGC	2186
rs560884478	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67850647	GCTAGGATTACGGGC[A/G]TGAGCCACTGTACCT	2186
rs560892663	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67951531	CTGTTTCCGTTCCAC[A/T]TTCTACACAGAGTGG	2186
rs560902693	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67927914	TTTTAGAGATGGAGT[C/T]ACTCTGTCACCCAGG	2186
rs560910983	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67933292	GTAAAGATCATGGCC[A/G]GGCACAGTAGCTAAA	2186
rs560918343	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67829899	CAATGCAAAGACATT[A/G]GTTGACATTACTAAA	2186
rs560930635	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67969268	CCTGGCCAACATGGT[A/G]AAACCTCATCTCTAC	2186
rs560949891	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67956085	GCACTTTGGGAGGCC[A/G]AGGCGGGCGGATCAC	2186
rs560975511	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67936458	AGAGAAACTGTAAAT[G/T]CTGGTATTACTATGG	2186
rs560977470	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67922187	AAAATCACTTCTCTT[G/T]GGCTTGTATCCCTTT	2186
rs560982952	in-del	-/GT	0.0316865	0.121816	intron-variant	BPTF	GRCh38.p7	17:67878685	TTTATGTGTTCGTGT[-/GT]GTGTGTGTGTGTGTG	2186
rs561023249	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67935867	AAACTGAAAAAAAGA[A/G]TTTTGTATAGGTATC	2186
rs561025672	snp	C/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67950233	GCCATTGCCCTCCAA[C/G]CTGGGCGACAGAGTG	2186
rs561032984	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67886439	TAATTTTTTAAATGA[A/G]AGTTTGGTGGGGGGT	2186
rs561058859	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67899540	TTTTTTTTCTTTTTT[C/T]TTTTTTTTTGAGACA	2186
rs561059680	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67837845	CTCACTTGCGATGTG[A/G]TATGAGACCCTGAGT	2186
rs561060445	snp	G/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67892862	TAAGGCCACTGTTTA[G/T]CTGATAGTCCACTAA	2186
rs561067737	snp	C/T	0.00358779	0.0422022	intron-variant	BPTF	GRCh38.p7	17:67964726	TTGTTCTTGGCCGGG[C/T]ATGGTGGCTCATGCC	2186
rs561087954	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67956895	CATGAACCCAGGAGG[C/T]GGAGCTTGCAGTGAG	2186
rs561089672	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67978540	CAGACCTCGTGATCC[A/G]CCTGCCTCAGCCTCC	2186
rs561125058	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67828025	CAACCTCCGTCTTCC[A/G]GACTCAAGCGATTCT	2186
rs561132484	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67963822	AGTGTTTGAAATGGT[C/G]CTTTATTGTAGGTTA	2186
rs561138574	snp	A/T	0.0539704	0.155153	intron-variant	BPTF	GRCh38.p7	17:67856923	GCTTGAAGGGGAGAA[A/T]GGTGGTTTAGGAATC	2186
rs561158162	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67942060	ATCCCAGCACTTTGG[A/G]GGGCCAAGGTTTTGG	2186
rs561173567	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67920439	GAGAGCAGCCATCTC[A/G]TCTGTCTGGTTTATT	2186
rs561188413	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67828449	AAGATTGATGGGTGT[A/G]CATATGCTGACTTAA	2186
rs561250627	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67905555	CTACAAAAACGTTTT[A/T]AAAATTAGCCAGGTG	2186
rs561261387	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67891259	CTCCTGTGGAGTTTA[A/G]TGTGTCCTTAAAAAT	2186
rs561264911	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67864997	ATTTTTAGTAGAGAC[C/G]GGGTTTCACCGTGTT	2186
rs561275129	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67867675	GGAGGAGTAGTGGTT[A/G]GGTATTTTGTAGAAA	2186
rs561277101	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67837899	TCTGTTTTGAGAGTT[A/T]CCTGGCCAAGTGGTG	2186
rs561316267	in-del	-/A			intron-variant	BPTF	GRCh38.p7	17:67858578	AAAAAAAAAAAAAAA[-/A]GTTTACTGCTGTGTT	2186
rs561324392	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67906718	AATTAAAAATAGATA[C/T]ATTTTTTATATCTAT	2186
rs561339169	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67897027	AGCACAAATAACCAA[C/T]ATCAAGAATAAAAAA	2186
rs561350201	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67870682	ATAGCCAAGAATAAT[A/T]TACAGCATAACAGGA	2186
rs561360930	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67975091	TCCGGAGATTCCAAC[C/T]GTGTTAGGAGCTAAG	2186
rs561379442	snp	A/G	0.000332939	0.012898	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67912699	AACTGTGATCAAGGT[A/G]GAAAAAGGCGATAAG	2186
rs561389215	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67906335	CTGCCCGCCTCGGCC[A/T]CCCAAAGTGCTGGGA	2186
rs561390792	snp	C/T	0.00438332	0.0466095	intron-variant	BPTF	GRCh38.p7	17:67968589	CGAGACCATCCTGGC[C/T]AACACGGTGAAACCC	2186
rs561406521	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67876384	ACTGGTCAGCAGTGA[A/G]CTGTGTTGCTGAAAA	2186
rs561443900	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67835810	AGCTGGGACTACAGG[C/T]ACCTGCCACCATGCC	2186
rs561457388	snp	C/G	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67974465	AATTCAATTCTGACA[C/G]TATCTACCTGAAGAT	2186
rs561487927	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67878005	CTTGATGGATGTTTA[C/T]GAAGTTAACACATCT	2186
rs561503794	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67895310	TGCACTCCAGCCTGG[A/G]TGACAGAGCAAGACT	2186
rs561511434	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67851524	CAGCATGTTTTAAAA[A/G]TAGAAAGAGAATAGA	2186
rs561562666	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67876603	CTGAGGTCAGGAGTT[C/G]GAGACCAGCCTGACC	2186
rs561569071	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67918513	TAAAAAAAAATGTTA[A/G]GTGCGTGTTATGCCT	2186
rs561578337	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67956951	CCTGGGAGATAGAGC[A/G]AGACTCCGTCTCAAA	2186
rs561626807	snp	G/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67940931	ATGAGACAAATAAAA[G/T]TTGAGTACATTAAGC	2186
rs561637397	snp	A/C	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67919710	AAATTTAAACTAAGA[A/C]TTCTGGAGGCCTGTG	2186
rs561655513	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67968068	ATAGGAGCCACGAGT[A/G]ATCGTATCAACACGA	2186
rs561681836	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67839072	TTTTCTTACATTTGT[A/G]TCTCCTTTTTCTCTT	2186
rs561711912	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67960231	GAGCATCCTTTCTGG[G/T]ATCTGTTCAAAGCCC	2186
rs561735309	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67979327	CCAAGGCACGTGGAT[C/T]ATCTGAGATCAGGAG	2186
rs561738869	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67948527	CTCCAGACTAGCAAC[C/T]CTGAGAGGTGAGCTT	2186
rs561740154	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67826594	CTCCCCCCCCCAACC[C/T]CCTTTTTTTCCTCTT	2186
rs561746169	snp	G/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67862091	AGTGATTCTTCTGCC[G/T]CAGCCTCCCAAGTAG	2186
rs561747749	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67973353	CACTCCAGCCTGGGC[A/G]ACAGAGCGAGACTGT	2186
rs561756840	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67883348	ATAATCCTTTGTGTA[C/G]TTATGCACAACTTGA	2186
rs561780820	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67980173	AACATGGTAAAACCT[C/T]GTCTCTACTAAAAAT	2186
rs561798852	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67848115	TTCCTTCTAGAAACA[A/C]ACATTATATAGAGAG	2186
rs561811997	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67947867	TTATCGTGCACACGC[A/C]CAGAGTTCTGAGTTT	2186
rs561841926	snp	A/G	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67882032	TAGAGACAGGATTTC[A/G]CCATGTTGGCCAGGC	2186
rs561855715	snp	G/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67903015	CACCACAGTCTTTAC[G/T]GGTAGGTGCAGTGAT	2186
rs561869542	snp	A/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67961014	CACTGATTTTTTTTT[A/T]CTTTAGTTTAATACA	2186
rs561871540	snp	A/C	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67854861	TTGATGTGGTATAAA[A/C]CTTTGTAACTTAATA	2186
rs561905180	snp	A/T	0.0368353	0.130617	intron-variant	BPTF	GRCh38.p7	17:67910815	AAAAAAAAAAATATA[A/T]ATATATAAATTCCTC	2186
rs561909106	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67923770	CAAGTGTGAGCCACC[A/G]CGCCCGGCCCTCTCT	2186
rs561923700	snp	A/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67972273	AGGAATCTCACTCTG[A/T]CACCCAGGCTGGAGT	2186
rs561964630	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67918207	TCCCACAGTGCTGGG[A/T]TTACAGGCGTGAGCC	2186
rs561995996	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67978594	GAGCCACCGTGCCCG[A/G]CCAGAAATTTTTGTT	2186
rs562002614	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67961625	GCCGAAGTGGGAGGA[C/T]CACTTGAGCCCAGGT	2186
rs562002777	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67954849	CTAGGAAGAAGTTCA[G/T]TCTCTCTCTATAAAT	2186
rs562014543	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67853114	ATACTCCAGCCTAGG[C/T]GACGGCTGTAGGTGA	2186
rs562019293	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67943305	AGGGATTCACATGTA[A/T]ATGGAGCTTACTTAG	2186
rs562035712	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67932334	AAGAAACATATAAAA[C/T]AAAATTACAAATGCA	2186
rs562051840	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67917526	ATTCATCATCCAGTT[A/G]TTCATGTTTTGAATA	2186
rs562058661	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67861253	TCCCACTGTCCCTCC[A/G]TGATACAAGCCAGTG	2186
rs562071449	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67966395	TTTGAGTACCATTAT[G/T]GTAGAGGAAGCTCAT	2186
rs562105450	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67906765	CTTGCTCGCGACAGA[A/C]TTATGATTTCTTTGC	2186
rs562133635	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67910542	TGGTGGCTCATGCCT[A/G]TAATCTCAGCACTTT	2186
rs562136759	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67884802	ATAAGTAATTTAGTA[-/T]TTTTTTTTTTAGTGT	2186
rs562141908	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67891265	TGGAGTTTAGTGTGT[C/T]CTTAAAAATTTACTA	2186
rs562169940	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67839731	CTCTGGTTTTTGGCA[A/G]CTATGAATAAAGTTG	2186
rs562174833	snp	C/T	5.01937e-05	0.00500942	intron-variant	BPTF	GRCh38.p7	17:67924496	ACTCTTATTAGATGC[C/T]AGATGCCTAACAGGC	2186
rs562179478	in-del	-/TTAA	0.0146672	0.084371	intron-variant	BPTF	GRCh38.p7	17:67917617	TGTTTTTGGTTTAAT[-/TTAA]TTAATTAATTAATTA	2186
rs562213875	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67940742	GAACTTATTTTGATA[C/T]GTTTTTAAATGTGCT	2186
rs562235111	snp	A/C	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67972703	TCCATAATATATACT[A/C]ACCTATGTGTTCTCC	2186
rs562260772	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67946512	GGAACACTTCGTTAG[A/G]TACATATAATATATA	2186
rs562274510	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67907257	TTTGGGAGGCTTGAT[-/T]TTTTTTTTTTTTTTT	2186
rs562278451	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67845148	AGGAGGTGCACCATC[A/C]ATTTGTTCCATTATT	2186
rs562356766	snp	A/G	3.46159e-05	0.00416014	intron-variant	BPTF	GRCh38.p7	17:67853926	TTGTAATGATGTCAC[A/G]TCTTTATCTACAGGT	2186
rs562373143	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67884783	TGAATAGCTAGCTCT[A/G]TAGATAAGTAATTTA	2186
rs562403745	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67938666	CATATACCAGGACTA[A/G]GAACATTCTTGGGAG	2186
rs562421578	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67862176	AGATGGGGTTTCACC[A/G]TGTTGGCCAGTCTGG	2186
rs562424935	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67941651	TAAATGGTGCCAGGA[C/T]AATTGAATATACATG	2186
rs562438305	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67883090	GGAGGCCCAGGTGGG[C/T]GGATCACAGATCAGG	2186
rs562438663	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67934832	AGCCAAGATGGTGCC[A/G]TCGCACTCCAGCCTG	2186
rs562455795	snp	C/T	0.00517822	0.0506191	intron-variant	BPTF	GRCh38.p7	17:67835822	AGGCACCTGCCACCA[C/T]GCCCGGCTAATTTTT	2186
rs562463815	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67846474	TCCTGTATGGTAGCC[A/G]CGAGACACATGGCTA	2186
rs562464513	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67897124	CTGAGGTCGGGAATT[C/T]GAGACCAGCCTGACG	2186
rs562467129	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67842631	ACAAAGATTTTTTGA[A/T]GACAAAGGCTGTGGT	2186
rs562470785	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67884212	GCGCAATCTCAGCTC[A/G]CTGCAACCTCAGCCT	2186
rs562484493	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67862627	TCTTTAATTGCTGAA[C/T]TGCTAGTTTTATCAG	2186
rs562503515	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67851886	ATTGTGGTTTTACTT[C/T]GCCTTTCCTTGCTAA	2186
rs562530996	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67877314	GCAGTTATTTATTCA[A/G]CAGCTATTTATTGAG	2186
rs562543174	snp	G/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67974952	TTCCGGAGGTTGGGG[G/T]ATGGGACTAAAAGTC	2186
rs562550246	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67967043	AGGCGGAGGTTGCAG[G/T]GAACAGAGATCGCGC	2186
rs562552433	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67973706	AGACAGGGTTTCGCT[G/T]TGTTGGCCAGGGTGG	2186
rs562558435	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67869317	TTCTGTGTGTTAGAT[C/T]ATGTATACAGTATAA	2186
rs562604441	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67850366	CTTTTGCCTCATGGT[A/G]TTTTTGTTTGTTTGT	2186
rs562606997	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67926247	CTCCTGAGCTCAAGC[A/G]ATCTGCCTACCAGGG	2186
rs562630302	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67948581	CTGAGAAGAGCTTTT[A/C]ATGTCTATGACATAG	2186
rs562633435	snp	A/G	0.000265274	0.0115138	intron-variant	BPTF	GRCh38.p7	17:67875785	TCTGTAATGGGGGGA[A/G]TCCTTCCCTTTTGTA	2186
rs562639218	snp	A/G	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67879348	GGTTTCACCATGTTG[A/G]CCAGGCTGGTCTTGA	2186
rs562664546	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67905265	AATACAAAATTTGCT[G/T]GGTGTGCTGGTACAC	2186
rs562675395	snp	A/G	0	0	intron-variant	BPTF	GRCh38.p7	17:67848207	ACAATAAATGTAGGG[A/G]TCAACTCTAAAAAAT	2186
rs562690759	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67904498	ATGCTAAAAAGGAGT[A/G]TTAGTTCATTAATCT	2186
rs562695015	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67876258	ACATTTTCAGTTTTT[A/G]AAATTAAAGTTATAC	2186
rs562717611	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67826829	ATTTGGACAGATTGT[A/G]GTACACAAACACGCA	2186
rs562736530	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67826738	GAAGCCTCTTGTTTT[A/G]CAAACCTCTTTGCAT	2186
rs562755881	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67834670	AACCCCTTTATCTCT[A/G]TCTTTATCTGTTAAG	2186
rs562760250	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67947564	GCAGGTGGTAAGCAC[C/T]CAGGCCATCTGGTAG	2186
rs562774094	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67933231	CCACTGTACTCCAGC[C/T]TGGGCAAAAAGAGTG	2186
rs562805827	in-del	-/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67977828	AGCTTGGGCGACAGA[-/G]GGGAGATTCCATCTC	2186
rs562815096	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67972850	ATGAACCAAGAATGT[A/C]CTAGTGTGATGTGTG	2186
rs562834677	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67883102	GGGCGGATCACAGAT[C/G]AGGAGTTCGAGACCA	2186
rs562840496	snp	A/G	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67855583	CCTCAGTGTTCCTGA[A/G]GGTTTCGAGAAGCTC	2186
rs562879969	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67839792	AACACAATACTTGTT[C/T]TTCTTGAGTAAATAC	2186
rs562886164	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67916672	TCGGGAGGCTGAGGC[A/G]GAAGAATTGCTTGAA	2186
rs562904365	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67924702	TGGTCCCACTTGACA[A/G]CATACATACATTTTT	2186
rs562925669	snp	C/T	0.0023933	0.0345097	intron-variant	BPTF	GRCh38.p7	17:67974614	TCCCACAAACCTCTC[C/T]TAAGGTTCAGTAATT	2186
rs562939985	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67861194	CTTTTTCCTTTATTG[G/T]TTGCTATGCCTTTAA	2186
rs562947242	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67943935	ACTGGCTGACCATTG[A/G]GGGAGCTTGAACTGG	2186
rs562983583	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67961675	AACATAGAGAGACCC[C/T]GTCTGTACAAAAAAT	2186
rs562994638	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67917243	GTTCGAGCTATTCTT[C/G]TTTCTCAGCCTCCCA	2186
rs563012201	snp	A/G	0.000399281	0.0141238	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67854761	AACCGAAGACTCATA[A/G]TGTAAGTAAATCTGG	2186
rs563012309	snp	C/G/T	0.00358779	0.0422022	intron-variant	BPTF	GRCh38.p7	17:67829368	TCTTCTAAAAAAAAA[C/G/T]GGGATACATGTGCAG	2186
rs563012506	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67947476	TCTTGTTTATAAAAT[C/T]ATTGCTATGGTTCAG	2186
rs563015944	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67979945	ACTTGGGAGGCTGAG[A/G]CAGGAGAATCACTTG	2186
rs563025085	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67946659	TCAGACATTATAGCA[A/G]TTCCTTTAAAGTTAT	2186
rs563027330	in-del	-/GGAATATTTTGTCAGTCTTTAGTATC	0.481087	0.0953875	intron-variant	BPTF	GRCh38.p7	17:67879041	CAGTCTTTAGTATCA[-/GGAATATTTTGTCAGTCTTTAGTATC]AGGAATATTTTGGCC	2186
rs563056135	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67939513	ACTAAAAAGAGGTTT[A/T]TGGAAAACTGTAGAG	2186
rs563064605	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67931208	AGGCGGAGGTTGTAG[C/T]GAGCCAAGATTGTGC	2186
rs563066583	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67888382	TCACGAGGTCAGGAG[C/T]TCGAGACCAGTCTGG	2186
rs563069826	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67896338	ACACTGGAGCAACAA[A/G]TGTCGAGATTGAATC	2186
rs563085756	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67954045	AGGCGGGAGTGCAGC[A/G]GTGCAATCACAGCAC	2186
rs563100426	in-del	-/CAT	0.0142736	0.0832652	intron-variant	BPTF	GRCh38.p7	17:67879667	TGGTACTGACATCTG[-/CAT]CTGGTGAGGGCCTTA	2186
rs563125746	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67955555	TCAGAGGCCGGGCAC[A/G]GTGGCTCATGCCTGT	2186
rs563126694	snp	C/G	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67882600	ACCAGTATTATTGTT[C/G]ACACTAAGACTACTG	2186
rs563127314	in-del	-/A	0.00676609	0.0577691	intron-variant	BPTF	GRCh38.p7	17:67828654	CTGCCTCAGCCTCCC[-/A]AGTAGCTGGGATTAA	2186
rs563153904	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67844539	GGCGTGAGCCACCAC[A/G]CCCGGCTAATTTTTT	2186
rs563176598	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67930924	GGTGCCACTGCACTG[A/C]AGTCTAAGTGACAGA	2186
rs563182805	snp	A/C	0.00159617	0.0282053	upstream-variant-2KB	BPTF	GRCh38.p7	17:67825048	CGGTCGCTTGGGCCG[A/C]CCCTCTCCGCGACTT	2186
rs563186440	snp	A/C	0.00398564	0.0444627	intron-variant	BPTF	GRCh38.p7	17:67909271	CACCGCACCAGGTCC[A/C]CCCCCCCCTTTTTTT	2186
rs563191722	snp	C/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67932486	AGTATCACTTGAGCC[C/G]AGGAGTTCAAGACCA	2186
rs563209148	snp	C/T	0.00398564	0.0444627	intron-variant, utr-variant-5-prime	BPTF	GRCh38.p7	17:67889676	AGCTGGGCATGGTGG[C/T]GGGCGCCTGTAATCC	2186
rs563219257	snp	G/T			intron-variant, missense	BPTF	GRCh38.p7	17:67946007	ACAGCCCCAAGTCAT[G/T]GCTGTGCCTCAGCTG	2186
rs563222705	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67858243	TTTTAAGAAATATGT[A/G]TAAAATATGTGTAAC	2186
rs563233006	snp	G/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67979376	ACATGATGAAACCCT[G/T]TCTCTACTAAAAGTA	2186
rs563249619	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67923616	TCCTGAGTAGCTGGG[A/G]TTACGGGGGTGTGCC	2186
rs563277052	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67909999	ACCTTGAAAAGAAGC[C/G]TCATTCATACCCATT	2186
rs563281834	in-del	-/A/T	0.00398691	0.0444912	intron-variant	BPTF	GRCh38.p7	17:67829586	TACCAGTTTCATTGG[-/A/T]TTTTTTAGTCTGTAC	2186
rs563300211	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67960335	CTTAATTGTTTTATT[A/T]TAAGCAGTTGTTTTT	2186
rs563336319	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67895204	TGGGTGTGGTGGCAC[A/G]TGCCTGTAGTCCCAG	2186
rs563356011	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67867496	GACCAGTATTGATAC[A/G]CTGTTACTAACTCAA	2186
rs563380921	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67951869	GAGACCAGCCTGGCT[G/T]ACACGGCGAAACCCC	2186
rs563392737	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67902937	TGTAGGTTTTGCTTC[A/G]TGTCTCTCTGAGAAA	2186
rs563420175	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67959387	GTTGGGTTTAAGATA[C/T]AAGAAAACTCTTGTT	2186
rs563424982	in-del	-/ATTG			intron-variant	BPTF	GRCh38.p7	17:67932170	TTGTGAGCTCTATTC[-/ATTG]ATATTATTTCATTTT	2186
rs563438781	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67930261	TGGAATGCAATGGCA[G/T]GATCTCTGCTCACTG	2186
rs563441996	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67916886	TTTGTCTACACCATA[A/G]TCAACCACTAAGTTC	2186
rs563490090	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67874450	TCTAGGTTTTGATCA[C/T]TGCAGTGTGCTGCCC	2186
rs563493458	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67937075	TCTAGTGGAAAAGGT[A/G]GATAATAATGAAGTA	2186
rs563501136	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67903412	TGATAAGGAAAGATC[A/T]TCTAGTGTAATTATC	2186
rs563501757	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67887696	TTAGCTCATGTAGTT[A/G]GGAAGTCCGAGCCAT	2186
rs563531233	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67838667	ATTTTTTTAGTAGAG[A/G]CGAGGTTTCACCAGC	2186
rs563532151	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67871315	GGCTTGGTGGTGCAC[A/G]CCTGCAATCCTAGCT	2186
rs563533209	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime	BPTF	GRCh38.p7	17:67984202	GTACTATTTATTCAT[A/T]TATATAAATATATAT	2186
rs563537314	in-del	-/ATATATATATATA			intron-variant, utr-variant-3-prime	BPTF	GRCh38.p7	17:67982011	TATATATATATATAT[-/ATATATATATATA]TTTAAATATTGGCTT	2186
rs563549706	snp	G/T	1.72573e-05	0.00293741	intron-variant	BPTF	GRCh38.p7	17:67944421	TTACTACTACACGTG[G/T]CTGGGCTAACAGAGG	2186
rs563572399	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67968070	AGGAGCCACGAGTAA[C/T]CGTATCAACACGAAT	2186
rs563591993	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67880942	TTGAAGAGGGTGTAT[A/G]TATATTATATATATA	2186
rs563627894	snp	G/T	0.00517822	0.0506191	intron-variant	BPTF	GRCh38.p7	17:67945224	ATTTTTTTTGTTTTT[G/T]TGTAGAGACGGGGTC	2186
rs563660535	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67900174	CAGTGGCGCCATCTC[A/G]GCTCACTGCAACCTC	2186
rs563685233	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67935321	GGTTTCAGCCACTTG[A/G]GAGGCTGAGGCAGGA	2186
rs563712565	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67907504	GGGATTACAAGTACC[C/T]GCCACCACGCCGAGC	2186
rs563745845	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67977915	GCTGGAGTGCAATGG[C/T]GCGATCTCGGCTCAC	2186
rs563746118	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67852276	TTATAGATACCTGTC[C/T]AATTTTTTCTTTTAA	2186
rs563774074	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67915439	CTTTACAACCCATCC[A/G]GTACTGGATAAATCT	2186
rs563799808	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67937655	TGGTGACATTGAAGG[C/G]ATGGGTAGCCAGTGG	2186
rs563827668	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67939609	TGGGCCAGGTGAGGT[G/T]GCTCATGCCTGTAAT	2186
rs563841681	snp	G/T	0.00318978	0.0398085	downstream-variant-500B	BPTF	GRCh38.p7	17:67984830	ACAGGGTTTCTCCAT[G/T]TTGGTCAGGCTGGTC	2186
rs563874978	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67857812	TTTTTTTTGAGACAG[C/T]GTCTCACTCTGTTGC	2186
rs563876216	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67958255	GAGGATCACTTGAGC[C/T]TGGGAGGTGAAGGGT	2186
rs563889836	snp	A/G	0.00358779	0.0422022	intron-variant	BPTF	GRCh38.p7	17:67916182	AGGATTCATAGTGCG[A/G]TAACACAGTGGAGAA	2186
rs563918372	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67858503	GAGGTTGCAATGAGC[C/T]GAGATGGCGCCACTG	2186
rs563919920	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67917311	CTTAGTTTTAGTAGA[A/G]ATGGGGTTTCACTAT	2186
rs563949997	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67952913	TTTTAATAAAGCTTA[C/T]ACCTTCATTACATCT	2186
rs563979062	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67979462	TGAGACAGAATCACT[G/T]GAACCTGGGAGACGG	2186
rs563987461	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67965137	ACAAGGTCAGGAGTT[C/T]GAGACCAGACTGGCC	2186
rs563992093	snp	C/G	0	0	intron-variant	BPTF	GRCh38.p7	17:67910793	CAACAGAGTGAGACT[C/G]CATCTCAAAAAAAAA	2186
rs563994200	in-del	-/T	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67938191	CTATTGGAGATCATC[-/T]TGGGTGGCTTATAAA	2186
rs564005359	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67853864	ATGTATTTTAGGGGG[G/T]TATATGTTCAAATAG	2186
rs564011303	snp	A/G	0.00478085	0.0486577	intron-variant	BPTF	GRCh38.p7	17:67958741	AGGCCGAGGCGGGTG[A/G]ATCACCTGAGGTCAG	2186
rs564013225	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67952455	TTCAGTAGAGATGGG[G/T]TTTCACCATGTTAGC	2186
rs564053464	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67910176	GGTTTTAAGGTTCAT[C/T]CATGTTGTAGCATTT	2186
rs564069557	snp	A/G	9.98652e-05	0.00706559	intron-variant	BPTF	GRCh38.p7	17:67947691	ACCTGTGGTGATTAT[A/G]AAATATGCGCTTTTG	2186
rs564132086	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67954646	ATTGAGATTGTTGTA[A/C]CTTATTTAAGCATGA	2186
rs564133807	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-5-prime	BPTF	GRCh38.p7	17:67889792	CAGCCTGGGCGACAA[A/G]AGCGAAACTCCATCT	2186
rs564175813	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67903041	GTGATTTCCTTTCCT[G/T]CCTGAGAAGGAGTTG	2186
rs564211899	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67954138	ACTACGGGTACGGGC[A/G]AATGCCATGCCACCC	2186
rs564227042	snp	A/C	0.0023933	0.0345097	intron-variant	BPTF	GRCh38.p7	17:67867655	TTTGATGGCCTTGAC[A/C]GTTGGGAGGAGTAGT	2186
rs564248863	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67854820	AGACTAGTTTCCTTC[A/G]TGATTGATGTAGCAG	2186
rs564271465	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67960501	AAGCTGTTTTTGACA[C/G]TTGTGACTTGTATTT	2186
rs564287865	snp	A/G	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67880959	ATATTATATATATAT[A/G]CACACACACACACAC	2186
rs564290106	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67931041	GGAAGCCAAGGGGGG[C/T]GGATCACAAGGTCAA	2186
rs564295248	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67909843	ACAGGAAAGGTACTG[C/T]GTTGTGTTTTCTTGA	2186
rs564295722	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67848143	GAGTTGCCTTTTGAG[A/G]TCTAGAAGTCTGAAA	2186
rs564349019	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67923699	TGGCCAGGCTGGTCT[C/T]GAACTCCTGACCTTG	2186
rs564393861	snp	A/T	0	0	intron-variant	BPTF	GRCh38.p7	17:67874709	CTTTAAAAATACTTA[A/T]TTTTTCCTCTTTAAT	2186
rs564414142	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67970779	AGCTGTTATAGACCT[A/T]CATCATTTTAAATTA	2186
rs564421966	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67966867	AGCACTTTGGGAGGC[C/T]GAGACAGGCGGATCA	2186
rs564428412	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	BPTF	GRCh38.p7	17:67825102	TCTTTCAGCATCAGT[C/T]TCCATAGGGGGAGGG	2186
rs564428967	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67923222	CACCACGCCCAGCTA[A/C]TGTTTGTATTTTTTG	2186
rs564463212	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67839690	ACAGTGCATTTATCC[A/G]TTCAATAGTTGGATA	2186
rs564466178	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67895304	CACCACTGCACTCCA[G/T]CCTGGGTGACAGAGC	2186
rs564470298	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67832016	CCTGCCTCAGCCTCC[C/T]GAGTAGGGGACTACA	2186
rs564491625	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67865259	CCTTTTATTTATCTG[C/T]GATTTAATATAGGCC	2186
rs564501089	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67937727	GGAGTTATGGTCAGA[A/G]AGGTGGAGGGTGGGT	2186
rs564510931	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67901157	AGAAGAAGCAAATCA[C/G]TAGATAAAATACAGA	2186
rs564530072	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67844652	GCAATCTGCCCATCT[C/T]GGCCTCCCAAAGTAC	2186
rs564531568	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67881976	AGTAGCTGGGATTAC[A/G]GGCGCCCACAACCAC	2186
rs564545283	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67970815	AATTAAAATTAACAG[C/T]CCCCATCAATAGATT	2186
rs564551051	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67964813	GACCATCCTGGCTAA[C/T]ACGGTGAAACCCCGT	2186
rs564568604	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67845030	TTACAGGCATGAGCC[A/G]CTGCGCCCAGCCTGA	2186
rs564574946	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67972046	AGAGATGTAAAATGT[A/C]ATATTTACCACTACT	2186
rs564598842	snp	A/G	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67839285	GGTTTGAGACCTTCA[A/G]TGTGTTGAATGTATT	2186
rs564603833	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67971553	GCTCATGCCTGTAAT[C/T]CCAGCCCTTTGGGAG	2186
rs564609240	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67931513	AATAATTTTTAAAAA[A/C]CTATGAAAGAACATT	2186
rs564660976	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67953325	GCAATGGCGCGATCT[C/T]GGCTCCTGCAACCTC	2186
rs564669703	snp	C/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67852420	AGATTCTTATATGAC[C/G]TCTTAGATATATATA	2186
rs564688511	snp	A/G	0.00279162	0.0372561	intron-variant	BPTF	GRCh38.p7	17:67965078	TGGGCGTGGTGGCTA[A/G]CACCTGTAATCCCAG	2186
rs564688783	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67891631	TCAATTTTTTGTGGA[A/G]TAATAGATGACTCAC	2186
rs564694031	snp	C/G			utr-variant-3-prime	BPTF	GRCh38.p7	17:67982442	TCCAATTATATTCTT[C/G]GCCAATTTTGTCCAA	2186
rs564727291	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67837943	AAATGGAGTTCTTCA[C/T]TGCTTCTTACTTAAC	2186
rs564740753	in-del	-/TAT			intron-variant	BPTF	GRCh38.p7	17:67910811	TCTCAAAAAAAAAAA[-/TAT]ATATATATAAATTCC	2186
rs564753485	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67895532	AGTGGCGCCATCACA[A/G]CTCACTGCAGCCTTG	2186
rs564766778	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67945304	AGGTGTGAGCCACCA[C/T]GCCTGGCCAGAATTC	2186
rs564767915	snp	A/G	0.00438332	0.0466095	intron-variant	BPTF	GRCh38.p7	17:67943445	ATTACAGTTCTGGAC[A/G]GAAGAGAGAGCGCCT	2186
rs564780564	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67908210	GTCAGCCAGGCTGGA[C/G]TGCAGTGGCACCATC	2186
rs564781648	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67940272	CACTGCCAACCAGGC[A/G]GGACCTTTGGATGTG	2186
rs564788984	snp	A/C	0	0	intron-variant	BPTF	GRCh38.p7	17:67830035	AAAGGCATATCGCTG[A/C]ATAATGCTTTAATTC	2186
rs564802839	snp	A/G	0.00438332	0.0466095	intron-variant	BPTF	GRCh38.p7	17:67843343	AGCTTTATTGCCCAG[A/G]CTGGAGTGCAGTGGT	2186
rs564806960	snp	A/C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67970291	CCTGTGGTCCCAGCC[A/C/T]GAGAGACTGAGGCAG	2186
rs564815456	snp	C/G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67958785	GCCTGGCCAACATGG[C/G/T]GAAACCCCGTTTCTA	2186
rs564851351	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67915536	TGGCTTCTGCCTTTT[C/T]CTCTCATGCCACCTT	2186
rs564861678	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67844120	AGTCTCACTCTGTCA[C/T]CCAGGCCGGAGTGCA	2186
rs564863787	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67837328	TGGATTGTTGCATTA[G/T]AGTGTGTACCATTTA	2186
rs564886323	in-del	-/ATGAACCCT	0.00517822	0.0506191	intron-variant	BPTF	GRCh38.p7	17:67873679	AGTGGGCAATGGTAA[-/ATGAACCCT]ATACAGACACATAGG	2186
rs564931269	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67864485	GTGAGCCAAGATTGC[A/G]CCACTGCACTCCAGC	2186
rs564937588	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67929865	TCACGCCTGTAATCC[A/G]AACACTTTGGGAGGC	2186
rs564959583	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67879386	ACCTCATGATCCACC[C/T]GCCTCAGCCTCCCAA	2186
rs564988043	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67916332	TTTCAGGTGGGCTCA[C/T]GCCTCCCAGCACTTT	2186
rs565032741	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67952146	AATCCCCGTCTCTGC[A/T]AAAGCTTCAAATATG	2186
rs565037243	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67886566	GAGCAGGGAAGAAAG[A/T]TCCTTTTCATACTCC	2186
rs565037565	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67928875	AATGAGCCACATTTC[A/G]TGCATTGGTGCCCTT	2186
rs565064003	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67976346	GGTGTGGTGACGCAC[A/G]CATGTAATCTCAGCT	2186
rs565107367	snp	G/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67920492	AGTCTGATATGTAAG[G/T]GGGTCAATAAAGGTT	2186
rs565124821	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67840296	TTTATTTGTAGAGAT[A/G]GGGTTTCATTATGTT	2186
rs565135322	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67850846	ATAAACATATTAAAT[A/G]CTCTGCATTGTTCTG	2186
rs565152207	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67851279	ATTTTCTGCTTTTTT[C/T]TTTTTTTTTTTAATA	2186
rs565157165	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67957556	GAATTTTTAAAAAAA[A/T]TTTTAAGTCAGATTT	2186
rs565158047	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67977007	ACTCTTAGATAAAAC[C/T]GACAATCTATAAAAC	2186
rs565179422	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67885912	AGTTGGGTCCTCACC[C/T]CCCCAAAAAAAGTCA	2186
rs565180554	snp	C/G/T			intron-variant	BPTF	GRCh38.p7	17:67931648	GCCTCGCTGGCACAT[C/G/T]CTCCTTCCTTTTATT	2186
rs565245367	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67896088	CTGCCTCAGCCTCCC[A/G]AGTAACTGGGACTAT	2186
rs565245621	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67921299	GGAGGCCGAGGCGGG[C/T]AGATCACTTGAGATC	2186
rs565247510	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67913365	GCCAACTAATGTACT[A/C]AAGTTTTTGTAGGGA	2186
rs565259548	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67899595	GAGTGCAGTGGTGCA[A/G]TCTCAGCTCACTGCA	2186
rs565270976	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67870594	AGGTAAATACCCAAA[A/G]TAATATCTAATCATG	2186
rs565273939	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67857309	GGGACTACAGGTGCC[C/T]GCCACCGTGCCCGGT	2186
rs565282734	in-del	-/TATC			intron-variant	BPTF	GRCh38.p7	17:67842191	TATGCTTTCAGTGTA[-/TATC]TATATGCATACATTG	2186
rs565298992	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67904948	ATTTTTCTGAAATTT[C/T]TATTCGTACTGCAGA	2186
rs565328134	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67906372	GTGTGACCACTGCGC[C/T]TGGCCTATAAATAAG	2186
rs565340068	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime	BPTF	GRCh38.p7	17:67982988	GTTGCCTTGAATATA[A/C]CAGTACAATTTGTCA	2186
rs565343627	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67852688	TTTCAGCTTTTGTAA[A/T]CTATATTGAATTAAA	2186
rs565354545	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67921327	ATCAGGAGTTTGAGA[A/C]CAGCCTGGCCAACAT	2186
rs565358107	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67892315	ATATAATTCTAAAGA[A/T]TTAAAGCCTTCTTTA	2186
rs565371764	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67926642	ATATTACTTTAAAAA[A/G]TTTATTTAAGATGCT	2186
rs565417998	snp	C/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67858074	TACAGGCGTGAGCCA[C/G]CGTGCCCGGCTAACA	2186
rs565452607	snp	G/T	0.00279162	0.0372561	intron-variant	BPTF	GRCh38.p7	17:67828641	TCAAGCAATTCTCCT[G/T]CCTCAGCCTCCCAAG	2186
rs565497732	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67863406	TCTCCTGCCTCAGCC[A/T]CCCAAGTAGCTGGGA	2186
rs565535027	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67828106	CCGGCTAATTTTTGT[A/G]TTTTTAGTAGAGATG	2186
rs565542455	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67952596	GAGCAGTTTTACGTG[C/T]AGAACGTACAGTTCC	2186
rs565548467	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67844334	CTCACTGCAAGCTCT[A/G]TCTCCTAGGTTCACG	2186
rs565555581	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67957002	CTTTAAAGGAAACGT[A/G]CCCGGCACGGTGGCT	2186
rs565616591	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67963870	GTACAAGCTCTGAGA[C/G]TCTGTTATTAGCTTA	2186
rs565617222	snp	C/T			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67897297	GGTGAGCCGAGATCA[C/T]GCCATTGCACTCCAG	2186
rs565622281	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67968993	TCTCAAAAAAATAAA[A/G]AATAAACAAAATAAA	2186
rs565655680	snp	G/T	0.0182019	0.0936463	intron-variant	BPTF	GRCh38.p7	17:67881849	GAGTTTTGGGGATTT[G/T]GGGTTTTTGTTTTTT	2186
rs565656091	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67894681	AAGATCAAAAGAGAT[C/T]TGGTATATGAAAATT	2186
rs565659237	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67900688	GAGGTTTGACCAAAA[C/T]GATACTAATATTTGA	2186
rs565698782	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67936115	TTCTTACTATAAAAC[A/G]TGGTTCCAGGGCATA	2186
rs565708685	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67914957	CATAATCCTTTCTGT[C/G]TAATGGAGGCATGGG	2186
rs565724002	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67895382	ATATGTTTTTGAGAA[A/C]AGTACATTTATGCCT	2186
rs565745804	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67944818	GGGAGAAAAGTGAAG[C/T]GTGGCAATTAGCCTG	2186
rs565762038	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67935385	TGAGCCACAATCTTG[C/T]CACTGCACCTCCAGC	2186
rs565808695	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67953061	CGTCTCCCCGGGTTC[A/C]CGCCAGTCTCCTGCC	2186
rs565833194	snp	A/G	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67922276	TATATGGGAAGGTTC[A/G]ATGCTTGTCCCTCCC	2186
rs565833801	snp	G/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67928162	GTGCTAGGATTACAG[G/T]TGTGAGCCACCGCAG	2186
rs565910095	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67867617	TTTCCTCTGGGTTGT[C/G]GGTTTCTCAGACTTT	2186
rs565915648	snp	A/G	0.0023933	0.0345097	intron-variant	BPTF	GRCh38.p7	17:67906511	TTCAATGAGCCGATT[A/G]TTTCACGAGGGTGCC	2186
rs565967787	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67915596	CCTCCAGTCATAAAA[C/G]ACTGGATGTGGTTTC	2186
rs566050509	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67878502	AGAAGTATTCAGTTC[A/C]ACAGTGTATGAGAGT	2186
rs566050569	snp	C/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67885944	TGAGTTAATAGCCTG[C/G]AAGACTTAAAAAAAT	2186
rs566056652	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	BPTF	GRCh38.p7	17:67983019	ATTACTCTGCACCAG[A/G]CTAAAATGAGTAAAA	2186
rs566117699	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime	BPTF	GRCh38.p7	17:67982487	GCAAAGTCAACGACA[A/C]CATTATCTTGTCAAG	2186
rs566137724	in-del	-/A			intron-variant	BPTF	GRCh38.p7	17:67961983	TGTCAAAAAAAAAAA[-/A]GAAAAGAAAAAAAGC	2186
rs566185641	snp	C/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67885512	GGAGAATCTCTTGAA[C/G]CTGGGAGGTGGAGGC	2186
rs566282124	snp	C/T	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67950388	GAAACCCCAGTGATG[C/T]CAACAATCAACGTTA	2186
rs566302994	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67883639	GAGTATCACTCTGTT[G/T]CCCAGGCTGGAGTGC	2186
rs566306603	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67870261	TTTTTTCTTTCTTTC[C/T]TTTTTTTTTTTTTTT	2186
rs566308634	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67919833	AATTTGCAGCGAGGA[A/G]GAAGCTCAGTATTGT	2186
rs566320227	snp	A/C/G	3.30062e-05	0.00406229	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67911592	TAAGAACAAAAAACC[A/C/G]CTCATACAGGAGGAA	2186
rs566321184	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67890605	GCTGCTCGCTCCAAA[A/G]GGGCAACATACTTGA	2186
rs566348877	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67863420	CTCCCAAGTAGCTGG[A/G]ACTACAGGCACATGC	2186
rs566408011	snp	A/G			intron-variant, synonymous-codon	BPTF	GRCh38.p7	17:67929011	CAGCACAGGTCAGAC[A/G]TTCCAAATTACAGGC	2186
rs566408095	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67849500	TCAATGAATAGCAAG[A/G]TTTGAAGGTAACTTC	2186
rs566421930	snp	A/G	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67856998	CATTGCGTTTTGAGG[A/G]TTGTGTTCTCAACTT	2186
rs566447556	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67981240	TTTTAGGGAATTTCT[A/G]TTGTTTTCCAGATTT	2186
rs566498070	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67863095	GGTGGCTTGAAAAAA[C/T]ATGAATTTATTGTCT	2186
rs566526658	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67956514	GTAGAGATGGTGTTT[C/T]GCCACGTTGGCCAGG	2186
rs566536395	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67964076	TGAACTGGAATGTCA[A/G]TCTTGAAAGTATTAA	2186
rs566536787	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67855610	GCTCTTCTGGGAAGC[A/C]TGTGGGCGAGGTCAG	2186
rs566540759	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67835847	ATTTTTTGTAATTTT[A/G]GTAGAGATGGGGTTT	2186
rs566542522	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67827390	CTCTAGGCTGGTGCC[C/G]AGATGCATTTGGTGA	2186
rs566562284	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67869751	CATTTTGGGAGGCTG[A/T]GGCGGGCGGATCACG	2186
rs566579636	snp	A/C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67890036	ATTTTAATTACCATA[A/C/T]CTTAAAAATCGGGGC	2186
rs566597278	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67962828	CTGGCTGACCTGCAT[A/G]TTCCTTGTAGTGTAA	2186
rs566604460	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67974618	ACAAACCTCTCCTAA[A/G]GTTCAGTAATTTGCA	2186
rs566620473	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67933834	GAGGCCGAGATGGGC[A/G]GATCACCTGAAGTCA	2186
rs566639625	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67980486	TTTCATTTGTACATC[A/G]TGGTTATTCCTCTGG	2186
rs566670875	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67855046	CAGCTCACGCCTGTA[A/G]TCCCAGCACTTTGGG	2186
rs566686440	snp	C/G	4.94376e-05	0.00497156	synonymous-codon	BPTF	GRCh38.p7	17:67940599	ACAACCCCCTCGCCC[C/G]CAACAAGGACAAGTG	2186
rs566696002	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67841501	TACTTTTTTTGACTA[C/G]TGATAGAATGACATA	2186
rs566729589	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67840989	CTCTTAACAGTGTCT[G/T]TTTCCCAGAGCATAA	2186
rs566742126	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67942065	AGCACTTTGGGGGGC[C/T]AAGGTTTTGGGAGGC	2186
rs566747256	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67860979	AACTTACTGACTTCC[C/T]GTGCCTGAATTCCTT	2186
rs566748177	snp	G/T	0.0341408	0.126114	intron-variant	BPTF	GRCh38.p7	17:67925759	AACTAGTTTTCCCTT[G/T]CATTTTATAAAACAT	2186
rs566769704	in-del	-/TTAA			intron-variant	BPTF	GRCh38.p7	17:67832354	TATAATTATAATGTT[-/TTAA]TTGTTTTGTCTGCTG	2186
rs566788723	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67961325	TAGTATACCAGGTTC[A/G]TTCACTCCCTATTTT	2186
rs566794836	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67833077	GCTGGGATTACAGGC[A/G]TGAGCCACTGCGCCC	2186
rs566827315	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67948793	AGAAGTTCGAGACCA[G/T]CCTGGCCAACATGGC	2186
rs566828036	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67858542	CCTGGGTGATGGAGT[A/G]AGACTCTGTCTCCAA	2186
rs566838810	snp	A/T	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67904028	GTCTTTGTATTTTAT[A/T]TATTTATTTATTTAT	2186
rs566850344	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67967108	TCTCAAAAAAATAAA[A/T]AAATAAATAAAATAA	2186
rs566866270	snp	G/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67847368	AAAAATAATAAATTA[G/T]CCGGGCGTGGTGGCA	2186
rs566891085	snp	G/T	0.00279162	0.0372561	intron-variant	BPTF	GRCh38.p7	17:67955467	GAATCAGGTTTTCCT[G/T]TGAGTTTTTTGTTTT	2186
rs566896037	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67944815	CATGGGAGAAAAGTG[A/G]AGCGTGGCAATTAGC	2186
rs566913550	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67875810	TTTGTAGTAAAAGCC[A/G]AATGTCACCTAAAAC	2186
rs566915764	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67873896	TCTTCAAAAAAGAAC[A/G]AAGGCTCCTTGGAGA	2186
rs566943463	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67972903	ATGAACCTACAGCAT[C/G]GATGTGCCAAGTCTT	2186
rs566958531	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67939836	AGTGAGCCAAGATCA[C/T]GCCACCGCACTCCAG	2186
rs566958743	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67957991	AAGTTGTACCACTAG[A/G]TAGCAGAAGAGGTGT	2186
rs567014147	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67870996	CAGGATGGTCTCGAT[C/T]TCCTGACCTCGTGAT	2186
rs567015094	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67868058	ATTTCTATGAGTATA[C/G]ATTCATGGATATTTT	2186
rs567029432	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67949909	AAAACAAAAATTAGC[C/T]GGACATGGTGGCAGG	2186
rs567091449	snp	C/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67877657	AGAGTCTCACTCTTT[C/G]ACCCAGGCTGGAGTA	2186
rs567094720	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67833355	GCCTCCAGAGTAGCT[A/G]GGATTACAGGCACAC	2186
rs567105613	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67863832	GGGTTTGTTTAGAAA[C/T]GAAAGTTGAAACTTA	2186
rs567153478	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67878373	TACATGTTTCTTGTG[C/T]ACATACATGTGCATT	2186
rs567158518	snp	A/C	0.000373559	0.0136616	intron-variant	BPTF	GRCh38.p7	17:67964173	AAGTAACATCATCCC[A/C]TGTGTTTTGAACTCA	2186
rs567166473	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67857085	CTTGTTCATCTACTT[C/T]AAAATCTTTTTTTGT	2186
rs567175946	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67910553	GCCTGTAATCTCAGC[A/G]CTTTGGGAGGCTGAG	2186
rs567183894	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67976002	TAATTCAACTCTTCA[C/T]ACTCTTTATACTATT	2186
rs567188248	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	BPTF	GRCh38.p7	17:67825429	CCGCCGCGCCGCTTC[C/G]CTCCGTCCCAGGCTC	2186
rs567205971	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67949255	CTGTAGTCCCAGCTA[C/T]TTGGGAGGCTAAGGC	2186
rs567274567	snp	A/G	0.00716266	0.059414	intron-variant	BPTF	GRCh38.p7	17:67864508	ACTCCAGCCTGGGCA[A/G]CAGAGTGAGACTCCA	2186
rs567288813	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67976006	TCAACTCTTCACACT[C/G]TTTATACTATTCTGT	2186
rs567290654	snp	A/G	3.30431e-05	0.00406454	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912938	AAGAGTATTCCACAC[A/G]AGACAAAGTGAAACT	2186
rs567323050	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67828902	ATTAACTCCTTAGAG[A/G]TAAGTATTGAGCTTA	2186
rs567336869	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67957848	GTGACAAAGTGAGAC[A/C]CTGTCTCCACATAAG	2186
rs567351038	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67950435	GAAGTTCTGGCAAAT[A/G]TGTTAAGCCAAGCAA	2186
rs567370452	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67934543	AAAGAAAAGAAAAAG[A/G]TATTAGATATTATAC	2186
rs567382137	snp	C/T	0.00279162	0.0372561	intron-variant	BPTF	GRCh38.p7	17:67981338	TTTGCCATATTTTCC[C/T]ATTTTATGATCTCCA	2186
rs567406925	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67855846	TGGAAAGGAGAGTTG[A/G]AACTTTATCAGTGTG	2186
rs567414267	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67957087	CCGGAGTTCGAGACC[A/G]GCCTGACCAACATGG	2186
rs567422246	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67885011	GGCCATTTTCTTTTC[C/T]TTTATGACTGTTCAC	2186
rs567423136	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67891003	CCTGGGCAATATGGC[A/G]AAACCCCATCTCTGC	2186
rs567426429	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67926433	GGGTTCACGCCATTC[C/T]CCTGCCTCAGCCTCC	2186
rs567445703	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67980724	GGAGGCCTAGGCTGG[A/G]CCTGCACAGTGAAGG	2186
rs567452609	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67836345	CAGTTTATATATTTT[A/G]CTAGAAATATGGCTT	2186
rs567454010	snp	C/T	0.0023933	0.0345097	intron-variant	BPTF	GRCh38.p7	17:67884409	GCATGAGCCACTACC[C/T]CTGGCCCCTCCCTTT	2186
rs567457412	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67828272	TACCTTAAGAAATCA[C/T]ATGTTGGTCTTCTTT	2186
rs567462065	snp	G/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67949452	TGGTGGCAGGCACCT[G/T]TAATCCCAGCTACTT	2186
rs567467561	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67848420	CTGTAATATAATTGT[A/G]CTCACGCTGTCATGG	2186
rs567512463	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67961376	TCTAAGGAGTGTTTC[A/G]TAATCTCTTGTCCCA	2186
rs567523991	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67963051	CATTACCATCAATGT[A/G]TTGTTTCTTTTTTCA	2186
rs567526075	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67835429	ATCTCTTTTTCTCTA[C/G]CCTTTTATTTGCCCT	2186
rs567561476	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67927019	TTGTGTAAAGTACTT[C/T]ATATTATATTCAGGT	2186
rs567574666	snp	A/C	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67826527	AAGAGGCGCATTGTT[A/C]AAAATGGAGATTGCA	2186
rs567635871	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67827121	GGAACGCGCGTCTTA[A/G]CTCATTTGATCGCTT	2186
rs567648041	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67897256	TGAGGCATGAGAATC[A/G]CTTGAACCCGGGAGG	2186
rs567649216	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67955056	GCACTTTGGGAGGCC[A/G]AGGCGGGCGGATCAC	2186
rs567656996	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67949043	ATTCTGTAGGTATTG[C/G]TAACCTGCTTTCTAG	2186
rs567662203	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67835776	GTTCACGCCATTCTC[C/T]TGCCTCAGCCTCCCA	2186
rs567663218	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67841565	TCATGATATTCGTCT[A/G]TTGTTTAATTTGTGA	2186
rs567678735	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67932792	CAAATTACTACAAAA[A/G]CTACAAAAGATAAAA	2186
rs567694142	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67883695	ACCTCCGCCCCCCTG[C/G]GTTCAAGCAGTTCTT	2186
rs567707343	snp	C/G/T	0.000566519	0.0168208	upstream-variant-2KB	BPTF	GRCh38.p7	17:67825502	CGCTGTCGGTTCCCC[C/G/T]AGTCACCGAGCGAGA	2186
rs567718301	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67869650	ACAATGAGCATGTTA[C/T]ATAGTTCAGTATGAT	2186
rs567732815	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67919056	GGGCTCCTGTAGTCC[C/T]AGCTACTCGGGAGGC	2186
rs567738363	snp	C/T	0.0115144	0.0749975	intron-variant	BPTF	GRCh38.p7	17:67873265	GAGTTCAAGACCAGC[C/T]GGGCCAACGTGGTGA	2186
rs567750905	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67967637	ACCAGCCTGGCCAAC[A/G]TGGCGAAATACGTCT	2186
rs567767187	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67890677	GCGGTGGTGAGGGAA[A/G]TATCTCCCCAAAGGA	2186
rs567776155	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67844379	CAGCCTCCCGAGTAG[C/G]TGGGACTACAGGCGC	2186
rs567783923	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67862285	CCGGCCTAGTTACTT[A/G]TTTTAAGGTAAATAT	2186
rs567797379	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67856327	TAAAAAAAATAGTAA[A/G]ATCCTGTTTCTGTGT	2186
rs567804411	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67847388	GCGTGGTGGCACATG[C/G]CTGTAATTCCAGCTA	2186
rs567816166	snp	A/G	1.66935e-05	0.00288903	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67911241	GTGTCAGAGTGACTC[A/G]ATGAGACAAGAACAG	2186
rs567825172	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67918084	GATTACAGGCATGAG[C/G]CACCATGCCCGGCCC	2186
rs567855372	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67980460	TTCTCATTATAAGCC[C/T]CTCTATGCTTTTTCA	2186
rs567911150	in-del	-/AA			intron-variant	BPTF	GRCh38.p7	17:67950051	GAATGAGACTGTCTC[-/AA]AAAAAAAAAAAAAAA	2186
rs567944294	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67868872	CTGTTGGGCACAAAT[A/G]TACTTTGTCTTCAGA	2186
rs567957343	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	BPTF	GRCh38.p7	17:67889823	CAAAAAAAAGAAAAA[A/G]AACCTCCATGATCTG	2186
rs567960206	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67902471	TCCTTCTCCTTAGTT[C/T]CAAGCGTGTTGGCAG	2186
rs567963302	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67952722	TATTAACGAAAGTCC[A/G]TAGTTTACATTAAGG	2186
rs568011971	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67934466	GGGGGTTGCAGTGAG[C/T]GGAGATTGCACCACT	2186
rs568058358	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67845096	TTGTGATAGGAATGC[C/T]GTATAAGTGCACGTC	2186
rs568083006	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67828451	GATTGATGGGTGTGC[A/G]TATGCTGACTTAAAT	2186
rs568095080	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67875916	AGTTTGATAAATGTC[C/T]TCGCAGTTAGTGCTT	2186
rs568100724	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67967227	CATCACTACAACCTC[C/T]GCCTCCCAGGTTCAA	2186
rs568143967	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67896038	GCGTGATCTCGGCTC[A/G]CTGCAGCTCCGCCTC	2186
rs568163284	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67973052	TTATATATATATATA[C/T]TTTATATATATATAA	2186
rs568166429	snp	C/T	0.000399281	0.0141238	intron-variant, missense	BPTF	GRCh38.p7	17:67945934	TTTCATCAGGACAAA[C/T]TTTAAATCAAGTTAC	2186
rs568175695	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67833145	GGAATCATATAATAT[A/G]TGTCTTCCATCATTT	2186
rs568176532	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67861340	TTCCAAGATTTTTTC[-/T]TTTTTTTTTTTTTTT	2186
rs568178370	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67955854	GATTCACTTAAATTA[G/T]CATTTATAGGCCAGG	2186
rs568223352	snp	A/T	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67909463	CTTTTTTTTTTTTTT[A/T]AATGAAAAAATGAAA	2186
rs568230805	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67965838	AGGGCAGGAGGATCA[C/G]TTGAGTTGACGAGTT	2186
rs568246686	snp	C/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67860849	AACAGGCGTGGACCA[C/G]CACACGCCTTTAAAC	2186
rs568273690	snp	A/G	0.00279162	0.0372561	intron-variant	BPTF	GRCh38.p7	17:67846337	GTATTTTAGCTTTGT[A/G]TTGACAACCCAGTGG	2186
rs568284401	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67880519	CTGTAATAGGTCATG[C/T]TCCCTTTATCATTTA	2186
rs568292732	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67977429	CTGAGGCATGAGAAT[C/T]GCTTGAACCCGGGAG	2186
rs568301101	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	BPTF	GRCh38.p7	17:67889462	CTATTACAGGACTTT[A/G]TAGATGGTCCCAAGA	2186
rs568302648	in-del	-/T	0.0146672	0.084371	intron-variant	BPTF	GRCh38.p7	17:67960345	TATTTTAAGCAGTTG[-/T]TTTTTTTTTGTATTA	2186
rs568320289	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67829010	GTAGATAAGAACTTG[C/T]AATAGATGAAGTTTT	2186
rs568321106	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67979209	CCTGTTAGCAAAGGA[C/G]TAGGTGCTACAGAGA	2186
rs568325762	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67906860	CCTTGCTAGGTCCTT[C/G]GGATATTTAGGTTCA	2186
rs568361054	in-del	-/T	0.00279162	0.0372561	intron-variant	BPTF	GRCh38.p7	17:67880391	TGTAGTTTAGTTTTG[-/T]TTTTTTTATGACGTC	2186
rs568363779	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67896182	TTAGCCAGGATGGTC[C/T]CCATCTCCTGACCTT	2186
rs568384440	snp	C/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67947066	TGAAACTCACTTATC[C/G]CTCCTTAGCTATAGC	2186
rs568400037	snp	A/G	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67867059	TGTGATCACCATCAC[A/G]TATGTGGTTCCTGGT	2186
rs568411428	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67845722	AGGCTGCAGTGAGCT[A/G]TGATAGCACCACTGC	2186
rs568426272	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67905136	GCCAGGCAGCCAGGC[A/G]CGGTGGTTCACGCCT	2186
rs568477368	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67923308	AGCAATCCACCCAAC[G/T]TGGCCTCCCAAAGTG	2186
rs568533615	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67960560	TAAACCGTAAATGTA[A/G]TTTCATTTTTTTGGT	2186
rs568543251	snp	C/T	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67924913	ACCACCATGCCCAGC[C/T]AATATTTGTATTTTT	2186
rs568600219	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67959950	TTTTGAAGAAAATGA[A/G]TATTTTGGGAGTGAT	2186
rs568615059	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67965401	CAAGTGATAGAGATA[C/T]ATTGAAGACATAGAA	2186
rs568615632	snp	C/T	0.000798403	0.0199641	intron-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67919112	GGGAGGCGGAGCTTA[C/T]AGTGAGCTGAGATTG	2186
rs568629893	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67930468	CCTCCCAAAGTGCTG[G/T]GATTACAGGCCTGAG	2186
rs568662585	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67831149	TGGATTGACAAGGAC[A/G]AGATAGCTGGTGGGT	2186
rs568674491	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67971085	CGGGGATGTAGTATA[C/G]TTTTTTTGTTTGTTT	2186
rs568693508	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67937226	TTTGGGAGGCTGAGG[C/T]GGGTGGATCGCCTGA	2186
rs568725397	snp	G/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67876679	GACATGATATCATGC[G/T]CCTGTAATCCCAGCT	2186
rs568759208	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67827300	TTTCACTCTATTTCT[A/G]AGGAAAAAGCCCTCC	2186
rs568768949	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67838853	CACTTATGCCATGAA[A/G]TCAGATTTTATCTTT	2186
rs568770449	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67931084	ATCCTGGTCAATATG[A/G]TGAAACCCTGTCTCT	2186
rs568772061	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67890480	CCCTTCTCCATCTCT[A/G]GATTTTAAAAACTGG	2186
rs568791825	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67933663	AAAGTGTAAAAAGCA[A/G]AACTATTTGAAATCA	2186
rs568806548	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67975079	AACTCTTATCACTCC[A/G]GAGATTCCAACCGTG	2186
rs568835986	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	BPTF	GRCh38.p7	17:67889902	ATCCAAAGTGACTTG[C/T]TTTCCAGCCTGGGGT	2186
rs568885902	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67835295	CAAGTGCTCTATAGC[A/C]ACATGTATTGCACCA	2186
rs568897546	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67869701	AAAAATTAGTTAAAC[C/T]GGCAGGGCACAGTGG	2186
rs568923157	in-del	-/A	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67927844	GTACCTTGGAGGAAT[-/A]TAAAAATATATATAT	2186
rs568933661	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67875954	ATCATAATTTTCATG[C/T]TTCTTAAACTTCATT	2186
rs568936032	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67841422	CTCAAATAAATAAAT[A/G]AAAAATAAATACCAC	2186
rs568988503	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67939776	TCCCAGCTACTCGGG[A/G]GGCTCAGGCAGGAGA	2186
rs569002543	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67867958	CGGGTGAGGAGTTAT[A/G]TTCTACCTTCTTGAA	2186
rs569003707	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67904010	AATTTTATTTTTGAC[A/G]TAGTCTTTGTATTTT	2186
rs569005107	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67927185	CCCTTAACTAGCTCT[G/T]TGGCCTTGGGCCAGT	2186
rs569073574	snp	C/T	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67874148	GAATATAATTAATAT[C/T]CATGAGTGCGTACTG	2186
rs569092632	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67947982	CGTTTTCCAGTCACA[A/G]AAAGTTTTTGTCTCA	2186
rs569102366	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67971729	GAATTGCTTGAACCC[A/G]AGAGGCAGAGGTTGC	2186
rs569107745	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67883176	ACAAAATTAGCCGGG[C/T]GTGATGATGGGCGCC	2186
rs569108173	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67978824	GATTAAGCCAAAGAA[C/T]GTCAGGGATAAAAAT	2186
rs569120237	in-del	-/A/AA/AAA	0.418653	0.184544	intron-variant	BPTF	GRCh38.p7	17:67934870	GCGAAACTCTGTCTC[-/A/AA/AAA]AAAAAAAAAAAAAAA	2186
rs569121573	in-del	-/TTATTA	0.0038793	0.0438703	intron-variant	BPTF	GRCh38.p7	17:67853596	CACAAATGCAGTTAT[-/TTATTA]TTATTATTATTATTA	2186
rs569127507	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67966295	AGCATCACTCAGTGA[C/T]GGCTCATCATGTAGG	2186
rs569131337	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67973140	AGCACTTTGGGAGGC[C/T]GAGGCAGGAGGATCA	2186
rs569134692	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67867175	TTCCACTGTAAATTA[A/G]GGATGCTATACATTT	2186
rs569137133	snp	A/G	3.30912e-05	0.00406749	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67874982	AAGACAGTGACGACA[A/G]AACACCAGATGATGA	2186
rs569171359	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67856545	CCAGTTGGAAGCTCT[A/G]AGCAAGTGGGTGGGC	2186
rs569175377	snp	A/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67861322	GTAACCCCCTACCCC[A/T]ACCTTCCAAGATTTT	2186
rs569184563	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67853200	ACATTTATATACTTA[C/T]ATATGTATATCTGGA	2186
rs569188002	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67860913	CAACTAAACTATGCT[C/T]TTAAATCTATACAGC	2186
rs569206332	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	BPTF	GRCh38.p7	17:67825353	CGCACCGCGCTGTGC[C/G]GAGCCCAGGCGCCCA	2186
rs569212449	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67847198	TTTAAAATGCTTACT[G/T]AGCACAATGTCTGGC	2186
rs569241277	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67960636	AAAATGTAGTCCAGC[G/T]TTTTAAAGCCACAGT	2186
rs569247212	snp	C/T	3.29462e-05	0.00405857	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67854154	TGCAGCTCTGGTGAG[C/T]CAAGAGCAGTGCACA	2186
rs569247630	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67972296	GCTGGAGTGCAGTGT[C/T]GTGATCTTGAATCAC	2186
rs569297710	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67961236	AGGCACACAGATACA[A/T]GTGCCCATTCCATCG	2186
rs569307274	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67917617	ATGTTTTTGGTTTAA[C/T]TTAATTAATTAATTA	2186
rs569310132	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67931656	GGCACATGCTCCTTC[A/C]TTTTATTCCATAGGC	2186
rs569318389	snp	A/G	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67882069	CGAACTCCTGACCTC[A/G]GGTGATCCGCCCACT	2186
rs569330163	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67944916	AGAGTGTACAGGGGA[C/T]AGCCAAGAAGCAGGG	2186
rs569344269	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67903263	ATAAATGTTTTTGTA[G/T]TCTTTGGTCTTCGTT	2186
rs569351199	in-del	-/G			intron-variant	BPTF	GRCh38.p7	17:67964796	CAAGGTCAGGAGATC[-/G]AGACCATCCTGGCTA	2186
rs569420806	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67954418	GAGAGGAGTTTTGTT[C/T]TTGTTTTCTCTCCCA	2186
rs569432944	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	BPTF	GRCh38.p7	17:67824723	CAAAGGAGAGGTAAG[C/T]TCTTGCTGAGGTGAT	2186
rs569441289	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67923373	TAAAAGAACACTTTA[A/G]TCATTTATTCAGTGC	2186
rs569450617	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67844752	CTGATTTTTTTATTT[A/G]TTTTTTTTGAGACGG	2186
rs569461731	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67882115	GGTAGAATTACAGGC[G/T]TGAGCTACCGTGCTG	2186
rs569465279	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67931244	TACTCCAGCCTGGGC[A/G]AAAGAGCGAGATTCT	2186
rs569486549	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67966038	CCAGCCTGAATGACA[C/G]AGCGAGACCCTGTCT	2186
rs569502762	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67966464	AAAATATTTCATGTA[C/T]CAAATTTAAAACTCA	2186
rs569527821	snp	A/G	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67888010	CAGGCAAGGTACTAC[A/G]ATTGATGCCTCCAGC	2186
rs569534108	snp	G/T	0.000798403	0.0199641	downstream-variant-500B	BPTF	GRCh38.p7	17:67984572	TACATAGACATTTTA[G/T]AGTTTCATCAACTAC	2186
rs569547104	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67922672	TTTACTCACTTACGT[A/G]TTGTCTTTGGCTGCT	2186
rs569563385	snp	A/G	0.0107246	0.0724382	intron-variant	BPTF	GRCh38.p7	17:67900501	TTTGGGAGGTGAAGC[A/G]GGAGGATTGCTTGAG	2186
rs569567103	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67923782	ACCGCGCCCGGCCCT[C/T]TCTCTTATTTTTAAT	2186
rs569575179	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67917014	TTTATTTTGAAATAC[A/G]TTTTTAGTATTTTTT	2186
rs569629347	snp	C/T	0.00279162	0.0372561	intron-variant	BPTF	GRCh38.p7	17:67924840	CAGCTCACCGAGCCT[C/T]GACATCCCTGGTTCA	2186
rs569652345	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67841048	CCACTTTTTTTCTTT[A/T]ACACATCTGGGGTTC	2186
rs569660833	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67952625	CCCATATTATTCCTC[A/C]CCCACCCACACACAA	2186
rs569674768	snp	C/T	1.65825e-05	0.00287941	intron-variant	BPTF	GRCh38.p7	17:67929319	AGTTTTTAATTATGG[C/T]TTCATCTTTTTTTAA	2186
rs569679106	snp	C/T			intron-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67929555	TTTTTAGAATGACTT[C/T]TTCCAAGATTAATCC	2186
rs569689889	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67853177	AACTCTCAGTTATTT[A/G]TATTGATACATTTAT	2186
rs569692588	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67888568	GCACTCCAGTCTGGG[C/T]GACAGAACGAGACTC	2186
rs569701510	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67858156	TCTGTCACCTTAACC[C/G]AGAAACTGCTGTGAG	2186
rs569723692	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67907845	AATTAATAATCTGAT[C/T]CTCAGTCCATATTCC	2186
rs569726455	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67937901	GGGCGGATCACCTGT[C/G]GTCAGGAGTTCAAGA	2186
rs569753506	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67921117	CAGGAGGCTGAGGCC[C/T]GAGAATTGCTTGAGC	2186
rs569786736	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67915787	CTCTCTTACAGCTCC[G/T]TGAGAACACAGACAG	2186
rs569815135	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67923903	CCCAGGCTGGAGTGC[A/G]GTGGCGCGATCTTGG	2186
rs569819910	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67960369	TGTATTAAAATACTG[C/T]AACTCATATTTTTGT	2186
rs569841143	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67965147	GAGTTCGAGACCAGA[C/G]TGGCCAAAAGGATGA	2186
rs569891539	snp	C/T	9.99367e-05	0.00706812	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912653	TCACAGAAGTCACCA[C/T]GATGACCTCCACAGT	2186
rs569897866	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67899818	ACAAGCATGAGCCAC[C/T]GCGCCCGGCCTATGC	2186
rs569913181	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67859844	TCAGTATCAGTCTAC[A/G]AAACAGCATTCAGGG	2186
rs569927613	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67827625	TTTTCGTTGAAGTAA[A/G]GTGTGTCATGTCTTT	2186
rs569946124	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67908429	CAAAGTGCTGGGATT[A/G]CAGGCATGAGCCACC	2186
rs569956271	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67873153	GAGTACTGTGGATAT[A/G]CATGGTATTAAGTGT	2186
rs569958224	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67865703	ATTATATGTGTTCCT[C/T]TATGTCTAGTCCTAG	2186
rs569979730	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67958935	TTGCACCATTGACAA[A/G]AGCGAAACTGCATCT	2186
rs570021571	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67830240	CTTGTGTTGCAGTCT[C/T]AGTCTTGTGTGAGAC	2186
rs570022240	snp	A/G	0.00438332	0.0466095	intron-variant	BPTF	GRCh38.p7	17:67964827	ACACGGTGAAACCCC[A/G]TCTCTACTAAAAATA	2186
rs570051493	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67936622	GAATCCCCTGTGAGG[A/G]TAGGGTTTGTATGAT	2186
rs570065368	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67938863	GGAAAAGAAATGGGC[A/G]GTGTGTGGAGAGTGA	2186
rs570077226	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67829604	TTTTAGTCTGTACTT[C/G]CTGGAGGAAGGCTGT	2186
rs570096026	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67872565	ATAAAAATTAGCCAG[A/G]TGTGGTGGTATGCGC	2186
rs570119834	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67832379	TGTCTGCTGGTATAT[A/T]TCTAAAATTTTTATG	2186
rs570136188	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67946825	ATCATCCAGCAACAT[C/T]TTGCAATGGCACATT	2186
rs570139091	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67844195	AGTGAGTCTCGTGCC[A/G]CAGCCTCCGGAGTAG	2186
rs570236459	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67936196	CTAATATGAAATATA[A/G]CAGGGTTTTTTGTTG	2186
rs570250249	snp	A/G	0.00438332	0.0466095	intron-variant	BPTF	GRCh38.p7	17:67942495	AGTTAGCAAAGACAT[A/G]GAGCAGAAAGAATTC	2186
rs570255351	snp	C/T	0.0023933	0.0345097	intron-variant	BPTF	GRCh38.p7	17:67839462	ATTCATAGAATTATA[C/T]TAGATCTTATAATAT	2186
rs570275578	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime	BPTF	GRCh38.p7	17:67983107	TATTAAAATTCAACT[A/G]TGGATGTATATGAAA	2186
rs570276486	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67845450	GAGTCTTACTGAAGA[A/G]TGGCCTCGAGTTCTT	2186
rs570289404	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	BPTF	GRCh38.p7	17:67983728	TTTTACTAGATTTTG[C/T]ACTAACTCATATTAG	2186
rs570296618	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67943053	ACCTAAGATACATAC[C/T]GAAGTAGTAATGAAA	2186
rs570311345	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67943598	CCCATAGGTAATTTG[A/G]CACGTATTGAAAGAC	2186
rs570317137	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67956821	ACAAAAAAATTAGCC[A/G]AGTGTGGTGGCGGGC	2186
rs570325876	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67976011	TCTTCACACTCTTTA[A/T]ACTATTCTGTCTAAC	2186
rs570334467	snp	A/T	0.00279162	0.0372561	intron-variant	BPTF	GRCh38.p7	17:67978302	GAAATATATATATAT[A/T]TATATATTTTTTTTG	2186
rs570340548	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67850471	TCTCCTGGGTTCAAG[C/T]GGTTCTTCTGCCTCA	2186
rs570342782	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67896174	TCACCGTGTTAGCCA[C/G]GATGGTCTCCATCTC	2186
rs570351222	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67908706	TGTTGGCTAGGCTGG[C/T]CTTGAACTCCTTGTC	2186
rs570366805	in-del	-/AG			intron-variant	BPTF	GRCh38.p7	17:67900128	TGTGTGTTTTGAGAC[-/AG]AGTCTTGCTGTGTCG	2186
rs570381320	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67871634	TTTTTCTGAGTAGAG[A/G]TGGCTTCTAAAACCT	2186
rs570400529	snp	A/C	0.000346103	0.0131504	synonymous-codon	BPTF	GRCh38.p7	17:67945677	ACAGTCATCCAAGCC[A/C]CAAGTTGCAGCACAG	2186
rs570410458	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67850954	ATGGCAATGCAGATA[C/T]AATAAACAAATGATA	2186
rs570413131	in-del	-/T	0.00517822	0.0506191	intron-variant	BPTF	GRCh38.p7	17:67840755	TTAGTAGAGATGGGG[-/T]TTTCACTATGTTGCC	2186
rs570443909	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67843244	TATATCTACATACAT[A/G]TAAATATATATCTAC	2186
rs570480242	snp	C/T	0.00953873	0.0683987	intron-variant	BPTF	GRCh38.p7	17:67900890	CTTGCTTGCCTGTAA[C/T]GCCAGCTGCTTGGGA	2186
rs570482698	snp	A/G	0.0023933	0.0345097	intron-variant	BPTF	GRCh38.p7	17:67972429	ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT	2186
rs570494210	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67846192	TCCAAACATTCAGAA[A/G]AGTTTTAAAAATATA	2186
rs570494238	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67869755	TTGGGAGGCTGAGGC[A/G]GGCGGATCACGAGGT	2186
rs570499534	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67882110	AAAGTGGTAGAATTA[C/T]AGGCGTGAGCTACCG	2186
rs570508208	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67852801	TAGATGTTTGCCAAA[G/T]TACCTTCTAAAAATC	2186
rs570511525	snp	C/T	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67930457	ACCTGTCTCGGCCTC[C/T]CAAAGTGCTGGGATT	2186
rs570517213	snp	C/G	0.000107774	0.00733999	intron-variant	BPTF	GRCh38.p7	17:67931860	TCTAAGTCCATTATA[C/G]TTTAATCTTTTTAAA	2186
rs570526067	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67960879	AAATGCCAAATGAAA[A/G]CTCTTTGTTGGCAGA	2186
rs570531742	snp	G/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67901562	ATTGACAAAGACCTT[G/T]TATAAATGAAAACTA	2186
rs570542733	snp	C/T	0.00557542	0.0525036	intron-variant	BPTF	GRCh38.p7	17:67896152	TATTTTTAGTAGAGA[C/T]GGGGTTTCACCGTGT	2186
rs570544476	in-del	-/GTTTTTTTTTT			intron-variant	BPTF	GRCh38.p7	17:67881858	GGATTTTGGGTTTTT[-/GTTTTTTTTTT]TTTTTTTTTTTTTTT	2186
rs570545696	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67979044	CCAGGCATGGTGATG[C/T]ACACCTGTGGTCCCA	2186
rs570566476	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67953107	GCTGGGACTACAGGC[A/G]CAGGCTGCAACGCCT	2186
rs570587383	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	BPTF	GRCh38.p7	17:67889422	CGGGAAATCTGACCC[A/G]GACCAAATGATGTCT	2186
rs570598598	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67951028	TTGTCAGGCTGGTCT[C/T]GAACTCCTGGCCTCA	2186
rs570603603	in-del	-/A			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67896689	TGAAAGGTAAGAAAT[-/A]ACACTTCTAAATAAA	2186
rs570642904	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67853315	GGTAAGCCACTTTTC[A/T]TTTCCCCCAGCATTG	2186
rs570647557	in-del	-/TTA	0.139455	0.224232	intron-variant	BPTF	GRCh38.p7	17:67853601	TGCAGTTATTTATTA[-/TTA]TTATTATTATTATTA	2186
rs570724872	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67935962	AGACATAATTAAATA[C/T]TGTGCTTATAAATTG	2186
rs570737861	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67902376	GAAATCCTACACAGT[C/T]CTCCTGGCATAGTCA	2186
rs570756026	in-del	-/C			intron-variant	BPTF	GRCh38.p7	17:67840332	GACTGATTTCAAACT[-/C]CTGGGCTCAAGCAAT	2186
rs570773264	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67953639	GGAGTGCAATAGCAC[A/G]ATCTCGGCTCACTGC	2186
rs570790794	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67875170	GTCCCCTCTTATAAC[A/G]TGTGTAACAATTGTA	2186
rs570851032	snp	G/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67930417	TTGGTCAGGCTGGTC[G/T]CAAACTCCTGACCTC	2186
rs570851144	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67970932	AGAAAACAGTCTCCA[A/G]GTGAAAGGGTCTAAG	2186
rs570852493	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67878237	TAGTAGCAGCTTATT[C/T]TTTTTTATTGCAGTA	2186
rs570854138	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67872635	CGCTTGAACCCAGGA[G/T]GCAGAGGTTGCAGTG	2186
rs570865402	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67857555	AACTGCAGCCTCGAC[C/G]TCCTGGGCTCAAGCA	2186
rs570878134	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67915939	CCTGGTGTTATTTCC[A/C]TTTTAAAATAAGGAT	2186
rs570924467	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67838756	GTTGGGATTACAGGC[A/G]TGAGCCACCACACCC	2186
rs570930300	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67830271	TTCTGAGAATACTTA[C/G]CTGGAATTTTAAAAC	2186
rs570930529	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67965913	ACATTAAAAAAAAAT[A/G]AGCTGCACATGTTGG	2186
rs570961612	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67893247	GACTTCAAAAGTTCT[A/G]TCATAAGATTTATCT	2186
rs570992107	snp	C/T	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67965297	GCAGTGAGCCAAGAT[C/T]GAGCCACGGCACTCT	2186
rs570998749	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67864781	TTGCATTATACTTAC[C/T]AGTTGATCATTCCTT	2186
rs571060621	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67838278	TCTTGACATTCATTA[A/G]TCTGTGATTTCGATA	2186
rs571074295	snp	A/G	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67871049	GTGCTGGGATTACAG[A/G]CGTGAGCCACCGCGC	2186
rs571075207	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67976867	ATTAAAGCCCCTGCA[A/C]TCTATGAGGGGTGGG	2186
rs571076076	in-del	-/TGAAA	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67928670	CAACCCTTTAGCTAC[-/TGAAA]TGAAACATTTTTTTA	2186
rs571079668	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67977362	TCTCCTTAAAATACA[A/G]AAATTAGGCAGGCAT	2186
rs571107409	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67968843	CAAAATTAGCCCGGC[A/G]TGGTGGCACATGCCT	2186
rs571138050	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67843827	CTGGAATGCAATGGC[A/G]CAATCGTGGCTCACT	2186
rs571143752	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67976348	TGTGGTGACGCACGC[A/G]TGTAATCTCAGCTAC	2186
rs571150193	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67937177	ATGAAAAGTACTGGC[C/T]GGGCGCGATAGCTCA	2186
rs571168473	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67957943	GGGTTTGTTCCTAGG[A/G]TAATAAGGTTTGCTT	2186
rs571173706	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67836445	TATGGAAGTTAAGAA[A/G]TATTTCAGAAATGCA	2186
rs571183931	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67917414	AGGTGTGAGCCACTG[C/T]GCCCAGCTGATATTG	2186
rs571188082	snp	A/T			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67886696	AGAGCTTTGGGCGAT[A/T]TTTTAGTTTTGGGGT	2186
rs571243295	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67975122	TGTCAGGAAATGGGG[A/G]CAAAAACCAAATATA	2186
rs571246684	snp	A/G			intron-variant, utr-variant-5-prime	BPTF	GRCh38.p7	17:67889454	AAAAGTATCTATTAC[A/G]GGACTTTATAGATGG	2186
rs571261108	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67942213	CCCAGCTGCTTGGGA[C/G]GCTGAGGCAGGAGAA	2186
rs571267680	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67899825	TGAGCCACCGCGCCC[A/G]GCCTATGCTGAGTTT	2186
rs571302125	snp	C/T	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67951736	TTTATACAGAAACAA[C/T]CTAACGAGGAAGAAA	2186
rs571303435	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67914845	TTTCACATTTTTTAA[G/T]GGGAGGAAATACCTT	2186
rs571306246	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67862378	GTACTACTCTAAACA[C/G]TTTATATATTTTAAT	2186
rs571311162	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67835945	GCTGGGATTACAGGC[A/G]TGAGCCACCATGCCT	2186
rs571322947	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67941323	CTGGGCGTGGTGGCA[C/T]GCGCTTGTAATCACA	2186
rs571329072	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67950354	ACATTAGAGATCTTC[C/T]AGTTAAAGTCAGAAA	2186
rs571334746	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67907516	ACCCGCCACCACGCC[A/G]AGCTAATTTTTGTAT	2186
rs571354715	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67975489	ATGTCGGTGTGTTTC[A/C]TTGATTTCAAACCAT	2186
rs571388871	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67928007	TTCTGCCTCAGCCTC[C/T]CGAGTAGTTAGAATT	2186
rs571415118	snp	A/G	1.65919e-05	0.00288022	missense	BPTF	GRCh38.p7	17:67975787	ACCTTGCCACCATGG[A/G]AGAAAGAGTACAAAG	2186
rs571417264	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67829476	TCCCCTTGCCCCCCA[C/T]CCCCCGGATGTGACA	2186
rs571433907	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67844935	TTTAGTAGAGACAGC[A/G]TTTCTTCATGTTGGT	2186
rs571434441	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67937516	AAGGACTCACTAACA[A/C]GATGAAATTTGGATA	2186
rs571435310	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67865553	AAATGAGTGTATTTA[A/G]AGCCAGATCTCTCCT	2186
rs571448718	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67842481	CACTTTTCTTCTTAG[A/G]CCTCTCCTCTAAACT	2186
rs571485187	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67829014	ATAAGAACTTGTAAT[A/T]GATGAAGTTTTGATA	2186
rs571549859	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67919809	CAGCAGCATTTTGTT[C/T]CGTTTAGGAATTTGC	2186
rs571566735	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67913805	TAAATAGATAGTGTT[A/G]GTAGTTGTAAAATCA	2186
rs571570843	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67921654	TGATTAAATTAACTT[G/T]GGAGTTCTTCTTGGA	2186
rs571571790	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67934617	GTGGTGGCTCACTCC[C/T]GTAATCCCAGCACAT	2186
rs571592305	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67884426	TGGCCCCTCCCTTTT[C/T]TTTTTTTCTGACAAG	2186
rs571592971	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67949483	GGGATGCTGAGGCAG[A/G]ATAATCGTTTGAACC	2186
rs571601739	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67898747	CCCAATAACATTCAG[A/G]TGGAACAAAAAAGAT	2186
rs571660563	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67879436	TGAGCCACCGCGCCC[A/G]GCTAGGGCTGGTGTT	2186
rs571667207	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67860354	CATGTAGAATTTTCA[C/T]GCAGTTTATAGTATG	2186
rs571693960	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, downstream-variant-500B	BPTF	GRCh38.p7	17:67983368	AGTTGATCATACTAA[C/T]GAGAACGGTAATGCG	2186
rs571735217	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67901888	TGGAGGATATAGGGG[G/T]GTACTCCCCAGGTTT	2186
rs571739956	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67838358	TCTAGTAAAACCTTT[A/G]AATTTTATTTTTGCT	2186
rs571745758	snp	A/G	4.94205e-05	0.0049707	synonymous-codon	BPTF	GRCh38.p7	17:67945797	ACTGTCTCCTGGACA[A/G]CAATCCCAGGTTCAG	2186
rs571751560	snp	A/C	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67879307	CCACCACGTCTGGCT[A/C]ATTTTTGTATTTTTA	2186
rs571754010	snp	A/G	0.00019857	0.00996221	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67874984	GACAGTGACGACAAA[A/G]CACCAGATGATGACC	2186
rs571755868	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	BPTF	GRCh38.p7	17:67982673	ACAGAAAACTTTTGA[C/T]TGTATTTATTTATTG	2186
rs571759057	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67962669	ACAGGAAAACTGGCC[C/T]GTGCCATATTCCATT	2186
rs571766846	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67856400	GACAGGTTTTTTTCT[C/T]TCCTCTGTGCATGGT	2186
rs571768629	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67855927	GCTTACGGAATCTTC[A/G]CTGTCTATGGTGTTC	2186
rs571789113	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67905077	TTGTTTTTTAGAAGA[C/T]GCCTCAGCCGCCTGA	2186
rs571794165	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67892381	ATTAAAGAACTGTAG[A/G]TGATTCACTGCTCAG	2186
rs571794734	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67851176	GACCCTAGCTCTTTT[C/T]GTAACGAGTTGTTTG	2186
rs571827159	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67885809	TTTGAGAGATAGTCA[C/T]ATCACTTGGTTATTC	2186
rs571836774	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67955234	AGTGAGCCCAGATAG[C/T]GCCACTGCACTCCAG	2186
rs571853054	snp	C/T			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67887225	TGTGGTTAAGTTTCT[C/T]ACATGTATTTGTTGA	2186
rs571855191	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67857832	CACTCTGTTGCCCCG[A/G]CTAGAGTACAGTGGC	2186
rs571862414	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67905816	GAAAGTGATAGAGGC[G/T]TCCAAAACACTGTCA	2186
rs571895197	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67956208	CCTGTAGTCCCAGCT[A/G]CTCGGGAGGCTGAGG	2186
rs571909258	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67957596	TTCTTATGGCCGGGT[A/G]TAAGTGGCTCATACC	2186
rs571959038	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67870196	GAAATAAGGTGAGTT[G/T]TACCTTGGATTTAAT	2186
rs571959103	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67862363	ACCCATGAAGTGCTG[A/G]TACTACTCTAAACAC	2186
rs571975287	in-del	-/TTAAAA			intron-variant	BPTF	GRCh38.p7	17:67921740	TAAATTTTAGCTTAC[-/TTAAAA]CAGCGGCCAGGTGCG	2186
rs571991407	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67892736	CATAGCAGCCCAGTA[C/T]ACATATTCAAAAGCT	2186
rs572005250	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67970053	AGCCTGACCAACATG[A/G]CGAAACCCTGTCTCT	2186
rs572016155	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67943219	TTTATAATTTTTAAA[A/T]TATACTTGGTGTTTT	2186
rs572031023	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67978689	TTTATACAGCAGGCT[A/G]TAAAATGTCAGCAGA	2186
rs572032025	snp	C/T	0.0298908	0.118541	intron-variant	BPTF	GRCh38.p7	17:67843231	AGATATATACCTATA[C/T]ATCTACATACATGTA	2186
rs572093108	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67837135	CATGAAGTGCCCCCC[C/T]TTTTATTAATACATA	2186
rs572153561	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67928714	TTTTCTTTTGCAGCC[A/G]GTTGAGCAAACAAGC	2186
rs572160180	snp	C/T	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67860013	ACAGTAAAATACTTA[C/T]GTTTGTCAATAAAAC	2186
rs572173312	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67827763	CACATAGGTTGTCCT[A/C]ACATAACTGAAAAAA	2186
rs572224225	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67963765	AATATGTAACATAGA[A/C]ATTAATGAGATTAAA	2186
rs572236629	snp	A/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67828367	CTGGTTAAAAAGAGC[A/T]GAGACATTTTGGCAG	2186
rs572241718	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67906640	CTCTTGACAGGATTA[C/T]GGTTTCTTTGCACTC	2186
rs572279310	snp	A/G	0.00358779	0.0422022	intron-variant	BPTF	GRCh38.p7	17:67950864	AAAAAATTCAGTAAC[A/G]TAGTCAGTTACAAGA	2186
rs572300001	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67864207	TTATATAAACTGTAT[A/G]TAGGCCAAGTAACTA	2186
rs572301287	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67906302	GCCAGGGTGGTCTCA[A/G]TCTCTTGACTTTGTG	2186
rs572315199	snp	C/T	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67835726	GCTGGAGTGCGGTGG[C/T]GCGATTTCGGCTCAC	2186
rs572330051	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67968536	GTAATACCAGCACTT[C/T]GGGAGGCTGAGGTGG	2186
rs572336949	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67836412	GAGGTCTGTGTATAG[C/T]ATATAGTATATTCTA	2186
rs572373971	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67926515	ATTTTTAGTAGAGAC[A/G]GGGTTTCACTGTGTT	2186
rs572442622	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67953696	TTCTCCTGCCTCAGC[C/G]TCCCGAGTAGCTGGG	2186
rs572446238	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67890431	CAACTTCTGATTTAC[A/C]CCCTTCCTGCTCATT	2186
rs572454189	snp	C/T	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67941531	GGAGAGGCAGATAGA[C/T]CAACAGAACAGTAGA	2186
rs572459085	snp	G/T			intron-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67918935	CCCAGCACTTTGGGA[G/T]GCTGAGGCAGGTGGA	2186
rs572507349	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67839570	TTTTAATTTTTAAAT[A/T]GTTTATACATGTACA	2186
rs572520282	snp	C/T	0.00597247	0.0543191	intron-variant	BPTF	GRCh38.p7	17:67968887	CTCGGGAGGCTGAGG[C/T]GGAGAATTGCTTGAA	2186
rs572539638	snp	C/T	3.31246e-05	0.00406955	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911423	CAGAAACAAAATGTC[C/T]GAAACAAAATTCCAT	2186
rs572578156	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67877980	AAGTTTATAAATATT[A/C]AGTGAATAACTTGAT	2186
rs572594719	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67897370	AAAAAAAAAAAAAAA[A/G]AGTAAAGAAAGAGAC	2186
rs572607771	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67905105	TGATTATCATTTTTC[A/G]AAATCTTAAATTTAG	2186
rs572608821	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67842518	ATGTATTTCCAACTT[C/T]CTGTGCTGTCCCAGA	2186
rs572673191	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67919500	GACTGTGGTCCACTA[A/T]TGTCTTCCAGTCTGG	2186
rs572684521	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67894782	AATCTTGTAGGCACT[A/G]TGCTAGGAATCTGAT	2186
rs572686134	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67925990	TGTAACCTAACATAT[G/T]ACTTTTTTTTTTTTT	2186
rs572716953	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67891768	ACATACACCAGATAC[A/G]AGTTTTGGTGAAATA	2186
rs572720647	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67938223	ATGAATCAGTACCAA[G/T]CCTTTTATCTGTCTC	2186
rs572764590	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67909340	ATATTTCACCAAAAA[C/T]GTTCACAAAGTTTTC	2186
rs572801543	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67892572	GTGGTGACAGGACAT[A/G]GTCCCAACTTTGTCT	2186
rs572811984	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67878917	AACTTGTTGTGATGT[A/G]TTTTCCTTGTTATAT	2186
rs572817045	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67949252	CGCCTGTAGTCCCAG[C/T]TACTTGGGAGGCTAA	2186
rs572838225	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67855382	TCCTCTATAGCCTAG[C/T]TCAGCTCATCCACCC	2186
rs572864728	snp	C/T	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67961970	CAGAGCAAAGCTCTG[C/T]CAAAAAAAAAAAAGA	2186
rs572878657	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67955775	GAGATTGCAGTGAGC[C/T]GAGATGACACCACTG	2186
rs572881596	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-5-prime	BPTF	GRCh38.p7	17:67889118	ACAGTGAGCTGCAGA[A/G]GCTGATGTAGATCTG	2186
rs572895322	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67856073	CTTCCTCTTTTCCCT[C/G]TTGTATTTATCTTGA	2186
rs572912470	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67925062	CCAGGTTTTTTTTTT[C/T]TTTTTTTTTTTAAGT	2186
rs572923346	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67948484	CAAGTCAGAGCTTTT[A/G]TAACTAAATGTGTAG	2186
rs572927889	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67973330	AGTGAGCTAAGATCC[C/T]GCCACTGCACTCCAG	2186
rs572953672	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67918103	CATGCCCGGCCCTAA[A/G]TTTTGTATTTTTAAT	2186
rs572961907	snp	C/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67868528	ATTTTCAATTTGAGG[C/G]TGGTTGAATCCAAGG	2186
rs572968630	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67861929	CCCTTTTTCTCTTGC[A/G]TCGTGAAATACTACT	2186
rs572972785	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67853761	TGGGAAAACTTTGCA[C/T]TTAGATTTTCTATAG	2186
rs572985851	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67869176	CCTTTTTGCTCTCCT[A/G]TGTTTTAGTACAACA	2186
rs572991962	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67979816	AAGGCCGAGGCGGGC[A/G]GATCACCTAAGGTCA	2186
rs573015884	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67924487	CCAGATTTCACTCTT[A/G]TTAGATGCCAGATGC	2186
rs573017500	snp	C/T	0.0023933	0.0345097	intron-variant, utr-variant-5-prime	BPTF	GRCh38.p7	17:67889636	AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAT	2186
rs573031369	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67881150	TGGGCAGATTTCATG[A/G]TACCCATTATATTGA	2186
rs573032199	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67972689	AGTCTTTTTCCTCCT[C/T]CATAATATATACTCA	2186
rs573055553	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67966897	ATGAGGTCAGGAGAT[C/T]GAGACTATCCTGGCC	2186
rs573068064	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67826646	GTCTCCACCGGGCAG[G/T]ATTGAAACTTTGGCA	2186
rs573089070	snp	G/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67960055	AGTAAAGTAAAATTT[G/T]CTATTTCACGTGTTT	2186
rs573098689	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67933165	CGGGAGGCTGAGGCA[A/G]GAGAGTCGCTTGAAC	2186
rs573107500	in-del	-/T	0.00358779	0.0422022	intron-variant	BPTF	GRCh38.p7	17:67853610	TTATTATTATTATTA[-/T]TTATTATTTCCTTAG	2186
rs573130396	snp	C/G	0.0023933	0.0345097	intron-variant	BPTF	GRCh38.p7	17:67961468	TCCTTCCAGAACACA[C/G]CCTATCACCCTGTGG	2186
rs573144737	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67833328	AGGCAATCTTCCTGC[C/T]TCAGCCTTCCAGCCT	2186
rs573157381	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67947321	TAGGGGAGACGAGGG[A/G]CAGTTCTTTAAAATT	2186
rs573158937	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67905508	GGCCAGGAGTTCAAG[G/T]CCAGCCTGGGCAACA	2186
rs573206131	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67834460	ATGTTACTAAGATCT[A/G]TCTGACTTTCTGCTT	2186
rs573226338	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67954326	GCATGAGCCACCGTA[C/G]TCGGCCCTGGTTGTC	2186
rs573232180	snp	C/T	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67896087	CCTGCCTCAGCCTCC[C/T]GAGTAACTGGGACTA	2186
rs573302787	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67846494	ACACATGGCTATTAA[A/G]TAAGCACCTGAAATT	2186
rs573310294	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67950628	GGATCATTTGAGGTC[A/G]GGAGTTCGAGACCAT	2186
rs573361756	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67932244	ATGTAACAGAAATCA[C/T]TAATAAATAAAATAT	2186
rs573392522	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67938836	TTTCTAAAAATATGT[A/G]TTAAATAAGTAGGAA	2186
rs573411090	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67942695	GGTAGCAGCATTGTT[C/G]ATAAGAATCAAAAAC	2186
rs573426954	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	BPTF	GRCh38.p7	17:67824862	TTAGGGCGCCCCTCC[C/T]TCCGGGCGTGGCAGC	2186
rs573448505	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67946495	AATGACTACTGTGGT[A/G]TGGAACACTTCGTTA	2186
rs573457598	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67867245	CCAACATGTTAGTTT[C/G]TTTCTTTAATTCAAG	2186
rs573469945	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67947049	CTCCCATTCACAGTC[C/T]GTGAAACTCACTTAT	2186
rs573470116	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67869810	AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAT	2186
rs573507694	snp	A/G	0.00358779	0.0422022	intron-variant	BPTF	GRCh38.p7	17:67953882	ACTGTGCCTGGCTGT[A/G]TAATTTCATTTGGAG	2186
rs573529701	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67907979	CTTCAAGGAGTCCAA[G/T]AACCATTGAAATAGA	2186
rs573577041	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67973932	GCGTTAGTGTTTGTG[G/T]TGTTCTGCATGCTGC	2186
rs573598642	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67899533	GCTGAGTTTTTTTTC[-/T]TTTTTTTTTTTTTTT	2186
rs573601573	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67876855	TATATGAAAACATAA[A/G]CAAGAAGTTTCAAGG	2186
rs573603736	snp	A/G	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67869299	AAAAAACAAAAAAAT[A/G]TTTTCTGTGTGTTAG	2186
rs573631916	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67848945	TCCATTTTTCTTCAG[A/G]ATTCATGCAGACCAC	2186
rs573644392	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67856114	TATTGAACGTTGGAC[A/T]TCCTATTTTGGTCTT	2186
rs573682369	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67905937	GATAGCATTAGGAGA[C/T]ATACCTAATGTAAAT	2186
rs573686823	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67949289	ATGATCACTTGAACC[C/T]GGAAAGCAGAGGTTG	2186
rs573690547	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67891002	GCCTGGGCAATATGG[C/T]GAAACCCCATCTCTG	2186
rs573692917	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67842124	TGTACATATGTGTAT[A/G]TATCTTTATACACTT	2186
rs573723034	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67940949	GAGTACATTAAGCTG[C/T]TTCCTTGCAAGACTC	2186
rs573738919	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67876206	ACATTGTTGTCAGAT[A/G]TATTTTGACATAAAA	2186
rs573741875	snp	C/T	8.27835e-05	0.00643311	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67911529	AAATGATTTTTTCAT[C/T]GATGACTCTAAACTA	2186
rs573746955	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67979330	AGGCACGTGGATCAT[C/G]TGAGATCAGGAGTCG	2186
rs573748150	snp	A/G	0.00478085	0.0486577	intron-variant	BPTF	GRCh38.p7	17:67862125	GGATTACAGGTGCCT[A/G]CCACCACACCCGGCT	2186
rs573759341	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67974173	CACTCTCTCAGATAT[G/T]TATGTCAAATTGTAT	2186
rs573774103	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67961658	TTGAGACCAGTCTGG[A/G]CAACATAGAGAGACC	2186
rs573783199	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67862583	CACTACTTGGGCTGC[A/T]TGACCAAGAGCTTAG	2186
rs573800794	snp	A/G	4.95348e-05	0.00497644	intron-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67918847	CGGACAGGTAAGGGG[A/G]AAGGGAGTTATTTTC	2186
rs573831051	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67826598	CCCCCCCAACCCCCT[C/T]TTTTTCCTCTTCAAA	2186
rs573841423	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67857362	AGACGGGGTTTCACC[A/G]TGTTAGCCAGGATGG	2186
rs573884599	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67962050	CGGGAGGCTGAGGTG[A/G]GAGGATCACATGAGC	2186
rs573894847	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67829671	AACTGGTTTAAGATA[C/T]CCGAATAACACATAA	2186
rs573902948	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67925829	CCTTATCTTCACTTA[C/T]ATCAAAGTTTGAGAT	2186
rs573919095	snp	A/G	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67846834	GCTTCTGGAGTAGCT[A/G]GGATTACAGGCACAC	2186
rs573930031	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67883091	GAGGCCCAGGTGGGC[A/G]GATCACAGATCAGGA	2186
rs573946792	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67826816	AAGGGAATTAAGGAT[G/T]TGGACAGATTGTGGT	2186
rs573952595	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67955934	GGGTGGATCAGTTGA[A/G]GCCAGGATTTTGAGA	2186
rs573958531	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67939858	GCACTCCAGCCTGGG[C/T]GACAGAGCGAGACTC	2186
rs574010203	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67827567	AAAAGCCTTTAAAAA[A/G]TAAAGTTTATGAGAA	2186
rs574023779	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67838716	CCTGAGCTCAGTCAG[C/T]CCTTCCTCCTTGGCT	2186
rs574025651	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	BPTF	GRCh38.p7	17:67889669	AAAAATTAGCTGGGC[A/G]TGGTGGCGGGCGCCT	2186
rs574036028	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67967522	ATTGTGGCAGTGTTT[A/G]TAATTACAAAAACAT	2186
rs574111730	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67947124	CATGAGATTATTGCA[A/G]TGATTAAATGAGGTC	2186
rs574114396	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67923563	TCTCGGCTCACTGCA[A/C]CCTCTGCCTCCTGGG	2186
rs574116303	snp	A/G			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67887784	CTTTTAGGTCTACAT[A/G]TATTTATGTGTGTTA	2186
rs574135247	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67970419	TAATAATAAAATACA[C/T]ATATACATACATACT	2186
rs574166539	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67925276	AAATTTCTGTAGTCT[A/G]TGAAAAAGCAAAGTA	2186
rs574189582	snp	A/G	0.00160224	0.0282587	intron-variant	BPTF	GRCh38.p7	17:67910621	CCTGGCCAACATTGC[A/G]AAACCCTGTCTCTAC	2186
rs574199538	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67974377	TCTGGTCAGCAAGAA[A/G]TGGGTGGGGATTTCT	2186
rs574226377	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67960252	TTCAAAGCCCTGCGA[A/G]TACATGAAATCCTGG	2186
rs574230123	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67933206	GAGGTTGCAGTGAGC[C/T]GAGATTGTGCCACTG	2186
rs574252273	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67916650	GGGCGCCTGTAATCC[C/T]GGCTACTCGGGAGGC	2186
rs574258766	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67903579	TTTCTTATGGAAAGG[A/G]TATAGTATTTCTTGT	2186
rs574321371	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67902895	TCTTCTGCCACTAGC[G/T]CTCTTAGAGACAAGA	2186
rs574333058	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67917195	TGGAGTGCAGTGGAG[C/T]GATCTCGGCTCACTG	2186
rs574341296	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67867403	GCAAAGATAGTAGAG[A/G]GTTTCCATATATCCT	2186
rs574369282	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67966208	TCTCTGCTACCTCAT[C/T]ATTAACCAGCTGTGG	2186
rs574394304	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67896256	CATGAGTGACTGCAC[C/G]CAGCCAATATTGGGC	2186
rs574401020	in-del	-/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67904547	AAATTGATTAGTAAA[-/T]TTTTTTTTGTCCCCA	2186
rs574414839	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67832548	TTTTAAAAGGTAACA[A/G]CTGTATGGAGATATA	2186
rs574439472	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67930873	GGGACGAGAATTGCT[C/T]GAACCCACAAGGCAG	2186
rs574453651	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67846712	CTTGTGTGGGTTTGT[C/T]TGTTTGTTTGGAGAC	2186
rs574475282	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67909942	TTTTAGTATATTCAC[A/G]AAGTTCAACCATTAT	2186
rs574481951	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67966755	TTTAGCAAGGCTGGT[A/G]GGGGTATAAATTGGT	2186
rs574519609	snp	A/G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67959004	AAAAGAAAATAGTGC[A/G/T]TTATGTTGCACTACT	2186
rs574547115	in-del	-/TAAT			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67897915	ATTAATATTTATTAA[-/TAAT]TAATAGCAAATAGGT	2186
rs574557506	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67839498	CACCCTTACATTCCT[G/T]CAGCAAACCTCTCTT	2186
rs574582659	snp	C/T	0.00914312	0.0669923	intron-variant, utr-variant-3-prime	BPTF	GRCh38.p7	17:67981860	TTCCCCTCATCAATG[C/T]AAATAAACACACACA	2186
rs574599083	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67901772	GTGAAGGTGTAGGAA[C/G]GCAGGGTGGCTTTAT	2186
rs574619519	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67966196	TCTAACATCACGTCT[C/T]TGCTACCTCATCATT	2186
rs574639917	snp	A/G	3.33322e-05	0.00408228	missense, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67875687	CTCTCAGAAACCCCC[A/G]ATAGCAGCAACATGG	2186
rs574641790	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67844526	TGCTGGGATTACAGG[C/T]GTGAGCCACCACGCC	2186
rs574663829	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67844934	TTTTAGTAGAGACAG[C/T]GTTTCTTCATGTTGG	2186
rs574686588	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67930586	TTTAAAGTTTTAAAT[C/T]TTTGAAAATGTTCTG	2186
rs574688152	snp	A/C	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67938221	AAATGAATCAGTACC[A/C]ATCCTTTTATCTGTC	2186
rs574692770	snp	C/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67888260	GTAATTGTATCTAGA[C/G]CTAAATCTAGTATTT	2186
rs574702248	snp	A/T			utr-variant-3-prime, downstream-variant-500B	BPTF	GRCh38.p7	17:67983299	TTTTATCATTCCCAG[A/T]CCATTGTCATCACGT	2186
rs574724786	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67839106	ATTACATTGCCCTCT[A/G]CCATTGATGGGAACC	2186
rs574727921	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67881756	TCTGCCCACCTCGGC[C/T]TCCCAAAGTGCTGAG	2186
rs574734288	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67952859	TTCTTGTTCCTCCTC[C/T]TTCCCCCTGTGCTAG	2186
rs574765041	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67844490	CTGACCTCGTGATCC[A/G]CCCGCCTTGGCCTCC	2186
rs574799393	snp	G/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67879800	GCTCTTTTTCTAACA[G/T]TCAGCTCTAGTGGGA	2186
rs574806471	snp	C/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67978338	GAGTCTCACTCTGTT[C/G]CCCAGGCTGGAGTTC	2186
rs574831246	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67942588	CTGGTAAAGTCAAAG[C/T]TGTGTATGCCCAAGG	2186
rs574865960	snp	C/T	3.44406e-05	0.00414959	intron-variant	BPTF	GRCh38.p7	17:67944417	GATGTTACTACTACA[C/T]GTGGCTGGGCTAACA	2186
rs574906666	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67865185	TGGCACTCAAAAACT[G/T]TTGGATCTTGGAGCA	2186
rs574908371	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67852873	GGGTGCGGTGGCTCA[C/T]GCCTGTAATCCTGGC	2186
rs574923663	snp	C/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67918027	CGTGGTCTCAATCTC[C/G]TGACCTTGTGATCTG	2186
rs574938057	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67922410	GTGATAGGGAAACAC[A/G]TGTTGTACACCCAAG	2186
rs574947794	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67872812	CTTTAAAATATAGGA[A/G]TTAAGGGCTGGGCAC	2186
rs574953582	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67922160	CTTTGATGCAAACCA[C/T]TGCAGTCCCCTAAAA	2186
rs575011457	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67865894	AGATATTATTTGAGA[C/T]AACTCCTTCAAAAAC	2186
rs575017893	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67953252	AGGCGTGAGCCACCG[C/T]GCCTGGCCTTTTTTT	2186
rs575036792	snp	G/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67872305	AACCAATTTAAATGG[G/T]CTAAACTTAGTAGGC	2186
rs575072090	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67916061	CTCTAGGAATTACTA[C/T]GGGGTATGGTCTGAA	2186
rs575110303	snp	G/T	0.000798403	0.0199641	intron-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67929617	GTGACAGAGTACTGA[G/T]TTGGAAAAAAATCTG	2186
rs575119720	in-del	-/A	0.391024	0.206427	intron-variant	BPTF	GRCh38.p7	17:67971827	GTGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA	2186
rs575156612	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67964786	TGGGCGGATCACAAG[A/G]TCAGGAGATCAGACC	2186
rs575179245	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67924406	AGGCATGAGCCACCT[C/T]GCACAACCAAATGTT	2186
rs575183598	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67842441	TTGTCTGAGTTACCA[C/T]CATAATATCAATGAC	2186
rs575211167	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67895676	TTATGTTGCCCAGGC[C/T]GTTCTTGAACTCTGG	2186
rs575221858	snp	C/T	7.46687e-05	0.00610973	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67826111	GGTGTACGATGACCA[C/T]GAGAGCGAGGAGGAG	2186
rs575221863	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67955117	ACATGGTGAAACCTA[A/G]TCACTACTAAAAAAA	2186
rs575239829	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67830425	AGATTCAAATTCAAG[C/G]AGAATTTGTCACTGG	2186
rs575247693	snp	A/G	0.000148808	0.0086245	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67911382	TCCAAAAGATCGAGT[A/G]TTAGATGATGTCTCC	2186
rs575281998	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67961434	GAGTGACTGAAAACT[A/G]AAATTCAAGTCCTGA	2186
rs575298555	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67903676	AGTTGGGGTTGTCTG[A/G]TTTGTAGGATTATAA	2186
rs575309558	snp	C/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67967389	TTGTGATCCGCTCCC[C/G]CTCGGCCTCCCCAAA	2186
rs575330632	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67979242	AATATTTACATTTTC[A/G]TAGTAACGTAAATAA	2186
rs575335234	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67954590	TGGAGCCTAGCAGGC[C/T]TGCAGTTTTAGTCCT	2186
rs575338010	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67861844	GCTAACTAGCTCATT[C/T]TTGAGGTCTCAGCCT	2186
rs575346457	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67896056	GCAGCTCCGCCTCCC[A/G]GGTTCACGCCATTCT	2186
rs575360816	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67876383	TACTGGTCAGCAGTG[A/G]GCTGTGTTGCTGAAA	2186
rs575387051	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67875446	TTTAAAATGGCCGTT[C/G]AATGGAAGCAGGTTT	2186
rs575412247	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67931418	TGAGCCAGGCTACGA[C/T]GAGCTGTGATTGCAT	2186
rs575461802	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67942906	TGTATAAGATTCAGA[A/C]ATAGGCAAAACTAAG	2186
rs575474081	in-del	-/C	0.00438332	0.0466095	intron-variant	BPTF	GRCh38.p7	17:67885909	AGAGTTGGGTCCTCA[-/C]CCCCCCCAAAAAAAG	2186
rs575486293	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67874455	GTTTTGATCACTGCA[G/T]TGTGCTGCCCAGACT	2186
rs575507709	snp	C/T	0.0023933	0.0345097	intron-variant	BPTF	GRCh38.p7	17:67881856	GGGGATTTTGGGTTT[C/T]TGTTTTTTTTTTTTT	2186
rs575519200	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67915442	TACAACCCATCCAGT[A/G]CTGGATAAATCTCAG	2186
rs575530879	in-del	-/TA			intron-variant	BPTF	GRCh38.p7	17:67880947	AGGGTGTATGTATAT[-/TA]TATATATATATACAC	2186
rs575533671	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67873356	CCAGCTACTTGGGAG[G/T]CTGGGGCAGGAGAAT	2186
rs575533751	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67865979	TATAAAGTTAGCTGG[A/G]TATCGTGGCACATGT	2186
rs575582642	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67836632	AAATACATGAGGACT[C/G]ATAAAACTCCAAGGA	2186
rs575587772	snp	C/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67839637	GTGTATCAGTAGTTT[C/G]TTTATTGCTGAGTAG	2186
rs575627034	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67878737	CTTTTGGGAGGTACC[C/T]GTCTGCTTCTTTGTT	2186
rs575630736	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67972607	TTTTGGCATATGGTA[C/G]TTTTTAACATTTTTT	2186
rs575656347	in-del	-/A			intron-variant	BPTF	GRCh38.p7	17:67839129	GGGAACCTGGGTAAT[-/A]AAAAAAAAAAGAAAA	2186
rs575670422	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67872908	GCAACATAGTGAGAC[A/T]CCATCTCTATTTTAA	2186
rs575671200	snp	A/C/T			intron-variant	BPTF	GRCh38.p7	17:67847240	ACTCTCTAGGCCAGG[A/C/T]GTGTTAGCTCACACC	2186
rs575679162	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67976342	GCCAGGTGTGGTGAC[A/G]CACGCATGTAATCTC	2186
rs575686682	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67852901	GGCACTTTGGCAGGC[C/T]GAGGTGGGTGGACCA	2186
rs575690291	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67937660	ACATTGAAGGGATGG[A/G]TAGCCAGTGGATCTC	2186
rs575716252	snp	C/G	0.0115144	0.0749975	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67887704	TGTAGTTGGGAAGTC[C/G]GAGCCATCATCAGGT	2186
rs575718407	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67953822	TGACCTCAGGTTATC[C/T]ACCCACCTCAGCCTC	2186
rs575718803	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67945261	TGTTGCTCAAACGAT[C/T]CTCCCACCTCAACGT	2186
rs575722933	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67845751	GCACTCTAGCCTGAG[C/G]GACAGCAAGATTCTG	2186
rs575749568	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67958764	GAGGTCAGGAGTTTG[A/C]AACCAGCCTGGCCAA	2186
rs575753180	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67970773	CACATCAGCTGTTAT[A/G]GACCTACATCATTTT	2186
rs575755238	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67862895	TAATTCCAATCTCCC[C/T]GTCACTATCTTTTCA	2186
rs575776245	snp	C/T	0.0023933	0.0345097	intron-variant	BPTF	GRCh38.p7	17:67916274	CTTTCTCTTTCACAG[C/T]GTTCATTTTTCCAAC	2186
rs575839796	snp	A/G	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67952040	AGCCTGGGCGACAGA[A/G]TGAGACTCTGTCTCA	2186
rs575845687	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67851991	ATTAGTGTTGAAATT[A/G]ATAATGAGTGTAATG	2186
rs575854598	snp	C/T	1.65411e-05	0.00287581	intron-variant, missense	BPTF	GRCh38.p7	17:67946227	CAAAGGGTTCAGCAA[C/T]TCAGGGATCAGCAGC	2186
rs575896681	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67908964	CTCAGCCTCCTGAGT[A/G]GCTGAGATCACAGGT	2186
rs575919112	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67850805	TTTTGGTTGTTTTCA[A/G]CTTGGTTGATTGTTT	2186
rs575930150	snp	A/G	0.00636936	0.0560724	intron-variant	BPTF	GRCh38.p7	17:67959265	CAAGCCAGGAGGGAC[A/G]CTCTTCCTAGCCACT	2186
rs575939010	snp	C/T	3.56271e-05	0.00422046	intron-variant	BPTF	GRCh38.p7	17:67922808	ATTTTAGAAGCAATA[C/T]TGCTTAAAATATTCT	2186
rs575946488	snp	G/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67929835	AATTTAAAATGCTGG[G/T]CCAGGTGCGGCGGCT	2186
rs575998887	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67830516	TGCGAGGTACGCAGT[A/G]CAGTGGGCATTTTAA	2186
rs576005433	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67886513	AACACAGCACTTGCA[C/T]TCAATGTTTTTGTTT	2186
rs576032904	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67837876	TTTACCTCCCAAATG[G/T]CAGGATGTCTGTTTT	2186
rs576035301	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime	BPTF	GRCh38.p7	17:67984007	GACTAATCGCTCAAT[A/T]TGAAAACATGAAAAA	2186
rs576043966	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	BPTF	GRCh38.p7	17:67823961	CTACAGGCACGCACC[A/G]CCACGCCTGGCTAAC	2186
rs576049286	snp	C/T	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67930581	AAAGGTTTAAAGTTT[C/T]AAATTTTTGAAAATG	2186
rs576072666	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67850404	CTGAGACAGAGTCTC[A/G]CTCTGTTGCCTAGGC	2186
rs576100230	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67951055	CTCAAGTAATCCACC[C/T]GCCTTAGTCTCCCAA	2186
rs576125490	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67863530	ACCTTGTGATCTGCC[C/T]GCCTTGGCCTCTCAA	2186
rs576125744	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67928761	TTACAAATAATGTTC[A/G]TAATATTACATTAGC	2186
rs576130009	in-del	-/A	0.999992	0.000150884	intron-variant	BPTF	GRCh38.p7	17:67826458	GCCTCCCCCCCAAAC[-/A]GAGGGGAAATGCGAC	2186
rs576162185	snp	A/G	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67957470	ACTTTGGGAGGCCAA[A/G]GTGGGCAGATCACCT	2186
rs576184562	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67977614	TTTGGGAGGCCGAGG[C/T]GGGCGGATCACGAGG	2186
rs576212411	snp	A/G			synonymous-codon, utr-variant-3-prime	BPTF	GRCh38.p7	17:67982270	TCATAACAACAAACT[A/G]CAGTCTACAGCTTCT	2186
rs576221707	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67907425	CAGTGGCATGGTCTC[A/T]GCTCACTGCAACCTC	2186
rs576276003	snp	C/T			synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67866560	TCTAGACAAAGATTA[C/T]TGGGAAGCAGAACTC	2186
rs576323555	in-del	-/ATT			intron-variant	BPTF	GRCh38.p7	17:67867697	TTGTAGAAAGCCCTC[-/ATT]ATGGGTTTTTCTCAT	2186
rs576325846	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67864262	CCGGTGCGGTGGCTC[A/G]TGCCTGTAATCCCAG	2186
rs576340612	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67899570	AGAATCTTGTTTGTC[A/G]CTCAGGCTGGAGTGC	2186
rs576348983	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67896205	CTGACCTTGTGATCC[A/G]CCCGCCTTGGCCTCC	2186
rs576354108	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67964559	GCAGTCCTTCACGTA[C/G]CAGTGCCATGAGCTT	2186
rs576414238	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67864950	GCTGAGACGACAGGC[A/G]CCTGCCACCATGCCC	2186
rs576417488	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67900769	AATCCCAACACTTTG[A/T]GAGGTTGAGGAGGGA	2186
rs576457863	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67906758	CCAGTATCTTGCTCG[C/T]GACAGAATTATGATT	2186
rs576460118	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67895026	GCATAAAGCAAAAAG[A/T]AAGAACCATTTTATC	2186
rs576469305	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67828728	TGACGGGGTTTCTCC[C/G]TGTTGGTCAGGCTGG	2186
rs576473697	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67871948	ATCATGTCTCAGCCT[C/T]CCAGGTAGCTGGGAT	2186
rs576479025	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67915040	CTATAAAAAGCCATG[C/T]ACGTGAAATGCATTT	2186
rs576481439	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67959454	TGGAGCTACTTTGAC[A/T]AGAGTGGGTAGTGTA	2186
rs576536091	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67935453	AAAAGGAAAGAAAAT[A/G]AGGGAGGAAATGAAA	2186
rs576573728	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67831526	CGTGTTTGGAAGTTT[G/T]TATTGAAACATGCGT	2186
rs576578659	snp	A/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67934806	GAACCCAGGAGGCAG[A/T]GGTCATGGTGAGCCA	2186
rs576607155	snp	G/T	0.000100035	0.0070716	synonymous-codon, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67891875	GGAGAAGTCCAACGG[G/T]GAGCTAAGTGAATCT	2186
rs576615854	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67871237	AGTTGAAAGAATTAT[A/G]CAGTTACCAGCCTGA	2186
rs576634362	snp	C/T	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67838548	GTGGCACAATCTTGG[C/T]TCACTGCAACCTCCA	2186
rs576670332	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67918570	GGACATATAATACCA[A/G]AGTCTTACAAAACCA	2186
rs576679683	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67884606	TTTTTCGTAGTGATG[C/G]AGTTTCACCGTGTTG	2186
rs576688193	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67936618	TCTTGAATCCCCTGT[A/G]AGGATAGGGTTTGTA	2186
rs576690792	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67974923	GATCAGCTTAACCTT[C/T]AGCCCCTCTCCCCTT	2186
rs576699049	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67968597	TCCTGGCTAACACGG[C/T]GAAACCCCGTGTTAG	2186
rs576701831	snp	A/G	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67937386	CGGACTTTGTCAAAA[A/G]AAAAAAAGAAAGAAA	2186
rs576702268	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67836163	GTTCTCCTGTATAAA[A/G]CGTCTTAGGAGTCAC	2186
rs576731792	snp	A/G	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67890053	TTAAAAATCGGGGCT[A/G]GAAATTTGTAGAAAT	2186
rs576751911	snp	A/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67878677	TTGAGCGTCTTTATG[A/T]GTTCGTGTGTGTGTG	2186
rs576755728	snp	A/G	0.0130921	0.0798413	intron-variant, utr-variant-3-prime	BPTF	GRCh38.p7	17:67981827	TTCTTTTGTTTTAGC[A/G]TAATTTTTCCCTTTA	2186
rs576776080	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67936891	TTGAGTAATTTCCCA[A/G]GCTATTAATCTGGGA	2186
rs576786520	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67842582	AGTTATAAAAGTTTA[G/T]GTTCAAAGCAAAATT	2186
rs576786961	snp	C/T	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67930741	TTGAGGCCAGGAGTT[C/T]GAGAACCACCTAAAC	2186
rs576815595	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67977648	GGAGATGGAGACCAT[C/T]CTGGCTAACACGGTG	2186
rs576844528	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67837249	GCTGTCCTGAATGTG[C/T]TAGAGATGTACCTTT	2186
rs576846995	snp	A/C	0.0596104	0.162024	intron-variant	BPTF	GRCh38.p7	17:67843206	CATCTACATACATGT[A/C]GATGTATGTAGATAT	2186
rs576847044	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67841975	ATGTTTTTGCTGTAG[G/T]AATTACAAAATATAT	2186
rs576850168	snp	A/C	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67866960	GTGACTGTACTGAAT[A/C]CCATAAGCAGTTGTA	2186
rs576885985	snp	C/T	0.0189856	0.0955633	intron-variant	BPTF	GRCh38.p7	17:67904014	TTATTTTTGACATAG[C/T]CTTTGTATTTTATTT	2186
rs576929676	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67907957	GTCTTTTATTCTGTT[A/G]TATAAACTTCAAGGA	2186
rs576941283	snp	A/G	0.0103295	0.0711199	intron-variant	BPTF	GRCh38.p7	17:67926386	CTGGAGTGCAGTGGC[A/G]CGATCTCGGCTTACT	2186
rs576969879	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67870720	AATTGTAGCCTGTCT[A/G]ATGACTTTGACTTGA	2186
rs576976154	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67921381	AATACAAAAAATTAG[C/T]CAGGTGTGGTGGTAC	2186
rs576981890	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67844820	ATGATCTCGGCTCAC[C/T]GCAACCTCTGCCTCC	2186
rs577049622	snp	C/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67929941	GGCAACATGGCAAAA[C/G]CCCATCTCTACAAAA	2186
rs577061930	snp	C/T	0.00119737	0.0244387	intron-variant	BPTF	GRCh38.p7	17:67957073	GGATCACCTGAGGTC[C/T]GGAGTTCGAGACCAG	2186
rs577064115	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67977012	TAGATAAAACCGACA[A/G]TCTATAAAACAAGAA	2186
rs577077240	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime	BPTF	GRCh38.p7	17:67984087	GTCCTTTTACTTTTT[A/T]AAAAAATGTTACATA	2186
rs577077734	snp	A/C/G			intron-variant	BPTF	GRCh38.p7	17:67958702	TGCCACTGCACTCCA[A/C/G]CCTAGGCAACAAAGC	2186
rs577091457	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67894926	AATCTACTTTTTAGC[C/T]CTGATAGACTTGCTT	2186
rs577095929	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67887491	GTTTTATTGAGGAGG[G/T]TTATCCCCATCCCAA	2186
rs577100293	in-del	-/G	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67834057	TTCTTTGTAGTTCTC[-/G]ACACACCTAACTCCT	2186
rs577110397	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67922071	CGTCCTGGCACAGAA[A/G]CAGCTCTGTTGATGG	2186
rs577132966	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67907446	CTGCAACCTCCACCT[C/T]CCGGGTTCAATCAAT	2186
rs577155774	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67888198	TGCAAAGATTTCACC[C/T]ACAACTTAAAACTTT	2186
rs577156190	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67958198	CTGAGTTTGGTGGCA[C/T]GTGCCTGTGGTCCTA	2186
rs577190223	snp	C/T	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67851300	TTTTTTAATAACCAC[C/T]ATATAGGAATAGACT	2186
rs577195968	snp	C/G	0.00517822	0.0506191	intron-variant	BPTF	GRCh38.p7	17:67892093	TAATTTTAATTACCA[C/G]ACCTTAAAAATAGGG	2186
rs577214013	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	BPTF	GRCh38.p7	17:67984693	GAGTGCAATGATGCC[A/G]TCTCGGCTCACCACA	2186
rs577257738	snp	A/G			intron-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67929844	TGCTGGGCCAGGTGC[A/G]GCGGCTCACGCCTGT	2186
rs577259003	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67940153	CTTTTTTGTCTTCCC[C/T]ATTATCATTTTGGTT	2186
rs577259625	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67903097	TAGGTCAATATGGGC[C/T]GACCTTCCTCATCCT	2186
rs577269584	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67865850	CTCCAGTTTGGGCTT[C/T]GATTGTCCAGAAGTA	2186
rs577295000	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67958609	TGGTGGGTGCCTGTA[A/G]TCCTAGCTAGTTGGG	2186
rs577300309	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67964851	AAAAATACAAAAAAT[C/T]AGCTGGGCGTGGTGG	2186
rs577321052	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67957305	ATAAAAAAATAAAAA[A/T]AATAAAGGAAACGTG	2186
rs577324357	snp	C/T			synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67912660	AGTCACCACGATGAC[C/T]TCCACAGTGGCCACA	2186
rs577331006	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67858330	CCATTTTTTGTTTTT[A/G]TCTTTGTTTTGACAT	2186
rs577332444	snp	A/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67892620	TTTGCAGGGTAGATA[A/T]GCAAGAATAAAGGAC	2186
rs577342191	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67879255	CAAGCGATTCTCCTG[C/T]CTCAGCCTCCCAAAT	2186
rs577346387	snp	A/T	0.0023933	0.0345097	intron-variant	BPTF	GRCh38.p7	17:67976074	CCTTAAATATCTTTA[A/T]AAAAAAAATAAATAA	2186
rs577376799	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67829673	CTGGTTTAAGATATC[C/T]GAATAACACATAAAG	2186
rs577381487	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67927670	ATGGTGTTTCTGTCT[C/G]CAATAAGCTTACCCA	2186
rs577383717	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67863289	TACCTTCTTTTCTTT[C/T]TCTTTTCATTTTTTT	2186
rs577406632	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67975563	ACCTTAACAGCAACC[C/T]GGATTTATATTTTAG	2186
rs577407464	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67950027	CCACTGCACTCCAAC[C/T]TGGGCAACAGAATGA	2186
rs577410220	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	BPTF	GRCh38.p7	17:67983262	TGTGCCTGGATTTCT[C/T]CAGGACAGCAGTGGC	2186
rs577477599	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67878732	ATCCTCTTTTGGGAG[A/G]TACCTGTCTGCTTCT	2186
rs577509598	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67846007	GTTCTTAAACTTTTT[C/T]GAAGCCAAAATTTTT	2186
rs577519035	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67850587	TTGGCCAGGCTAGTC[C/T]GGAACTCCTGACCTC	2186
rs577531899	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67884396	GTTGGGATTACAGGC[A/C]TGAGCCACTACCCCT	2186
rs577593033	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67974326	TTCCTGTGCTCTCAC[G/T]CTACGGTCAACGTGG	2186
rs577629610	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67969823	AAAAAATGCTCAGGA[C/G]GCTGAGGCAGGAGAA	2186
rs577659685	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67857210	GCCCAGGCTGGAGTG[C/T]GAGTGCAATGGCGTG	2186
rs577666623	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67842660	GTCCACAATGAAAAT[A/G]TAAAACATGTCTCTA	2186
rs577670353	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67882171	ATAAAATGTTTGAGG[C/T]TTATGTTACACAGTA	2186
rs577670964	snp	G/T	0.000798403	0.0199641	utr-variant-3-prime	BPTF	GRCh38.p7	17:67982567	AAAAAAAAAGAAAAA[G/T]AAAGCAAGAAAAAAA	2186
rs577675569	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67968434	GTTTACTAAAATAAT[A/C]AGTTAATTATGCTGG	2186
rs577682963	in-del	-/TTTTTTTTTTT	0.296873	0.245566	intron-variant	BPTF	GRCh38.p7	17:67857149	GTTCGTCTTTAACAA[-/TTTTTTTTTTT]TTTTTTTTTTTTTTG	2186
rs577694880	snp	A/C	0.00318978	0.0398085	intron-variant	BPTF	GRCh38.p7	17:67834992	CTGAGGTGGGAAGAT[A/C]ACTTAAGGCAGCAGT	2186
rs577696450	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67841791	GTGTTTTGGACCATT[C/T]ACATTTAATATGATT	2186
rs577724246	snp	A/C	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67950631	TCATTTGAGGTCAGG[A/C]GTTCGAGACCATCCT	2186
rs577728371	snp	C/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67969379	ATCAGTTGAACCTGA[C/G]AGGCAGAGGTTGCTG	2186
rs577732952	snp	A/G	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67845798	TATTTTATTTTATAT[A/G]TATTTATAACTATGT	2186
rs577756175	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67835688	TTTTTTTTTTTGAGA[C/T]GGAGTCTCGCTCTGT	2186
rs577840906	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67828291	TTGGTCTTCTTTGCA[C/T]CCAGAGCCGGTAATT	2186
rs577851483	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67942571	AACTTCCTGGACATG[A/G]TCTGGTAAAGTCAAA	2186
rs577894096	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67940743	AACTTATTTTGATAC[A/G]TTTTTAAATGTGCTG	2186
rs577895120	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67956729	AGCACTTTGGGAGGC[C/T]GAGGCGGGCAGATCA	2186
rs577911097	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67925892	TCTGTCACAGGAAAC[C/G]AATCACTAAACCCAA	2186
rs577925864	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67878496	GGTTGTAGAAGTATT[C/T]AGTTCAACAGTGTAT	2186
rs577933551	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67877107	CCAGATTTTAAAGAG[A/G]AGTTTGGTACTTTTG	2186
rs577965832	snp	A/C	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67949222	TACACAAAATTAGCC[A/C]AACATGGTGGCATAC	2186
rs577971547	snp	G/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67933990	TGGAGGTTGCCGTGA[G/T]CTGAGACCCTGCCAT	2186
rs577991155	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67953023	TGGAGTGCAGTGGCA[C/T]GATCTCGGCTCACTG	2186
rs578010722	snp	A/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67962127	CAGCCTGGGCTATAC[A/G]GCGAGACAAAAGAAA	2186
rs578031804	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67830024	TTGCTTAAGCTAAAG[A/G]CATATCGCTGAATAA	2186
rs578043547	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67832666	TACCTAATTCCAGCA[C/T]GTTTTTATACCCCCG	2186
rs578044236	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67926473	GTGACTATAGGCGCC[C/T]GCCACCACGCCTGGC	2186
rs578058975	snp	A/T			intron-variant, utr-variant-3-prime	BPTF	GRCh38.p7	17:67981481	TGGAATCAGAACTGG[A/T]TGTTGGGGTCACTCT	2186
rs578073236	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67952281	TTTTTTTTTTTTTTT[-/T]GGAAATGGAGTCTTG	2186
rs578077769	snp	A/G	0.00159617	0.0282053	intron-variant	BPTF	GRCh38.p7	17:67847692	AAAAAAAAAAAAAAA[A/G]AAAAAAGAAAGCACT	2186
rs578179880	snp	C/T	0.000798403	0.0199641	intron-variant	BPTF	GRCh38.p7	17:67933245	CCTGGGCAAAAAGAG[C/T]GAGACTCCGTCTGAA	2186
rs578191805	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67893982	AACTATTGTGCTTTT[A/G]ATTTAAGGTCAACCT	2186
rs578199574	snp	C/T	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67979972	CTTGAACCTTGGAGG[C/T]GGAGGTTGCAGATCG	2186
rs578237519	snp	C/G	0.000399281	0.0141238	intron-variant	BPTF	GRCh38.p7	17:67890756	CTTAATTATTTTCCC[C/G]AAAATGCATAGCCAG	2186
rs578251048	snp	A/G	0.00199481	0.0315187	intron-variant	BPTF	GRCh38.p7	17:67890115	TATTTCCAAAACTGT[A/G]GTAGTGTGATATTTT	2186
rs578253507	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67897294	TGCGGTGAGCCGAGA[C/T]CATGCCATTGCACTC	2186
rs745308171	snp	A/T	1.6473e-05	0.00286988	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67854073	GAATGTCATTGCCAT[A/T]TACGAGGTACTGCGG	2186
rs745312801	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67840277	AGTTGGCTAATTTTT[A/T]ATTTTTATTTGTAGA	2186
rs745327688	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67938553	GAGGCATTATATGTG[A/G]GAATTGGCTGCATGA	2186
rs745338872	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67876672	TTAGCTGGACATGAT[A/G]TCATGCGCCTGTAAT	2186
rs745346839	in-del	-/TTT			intron-variant	BPTF	GRCh38.p7	17:67881494	TCCATAATCAAGGTT[-/TTT]TTTTTTTTTTTTTTT	2186
rs745403758	snp	C/T			intron-variant, utr-variant-5-prime	BPTF	GRCh38.p7	17:67889356	GTATTGGATTGTTGG[C/T]TCTGAATTAGGAAGC	2186
rs745420314	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67827458	TAGTCACAATTTACT[A/G]AATTGTGAAATTAAC	2186
rs745420480	in-del	-/AT			intron-variant	BPTF	GRCh38.p7	17:67910812	CTCAAAAAAAAAAAT[-/AT]ATATATATAAATTCC	2186
rs745437922	snp	A/G	1.66891e-05	0.00288864	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912113	TTCAAATAAATGGAA[A/G]AGATAATAAACCCAA	2186
rs745461132	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67909428	ATTATATGGTACCTT[A/G]TACTCAATAAGACCT	2186
rs745488771	snp	G/T	2.80218e-05	0.00374301	intron-variant	BPTF	GRCh38.p7	17:67910839	ATTCCTCCTTTCAGA[G/T]TAAAAATTACATTTA	2186
rs745489803	in-del	-/AAAC			intron-variant	BPTF	GRCh38.p7	17:67968997	AAAAAAATAAAAAAT[-/AAAC]AAAATAAATAAAGAA	2186
rs745489977	snp	A/G	3.29451e-05	0.00405851	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67854231	AAGAAGACACTTCCA[A/G]TACTACCTTTGGACC	2186
rs745499422	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67829013	GATAAGAACTTGTAA[C/T]AGATGAAGTTTTGAT	2186
rs745543931	snp	G/T	1.65004e-05	0.00287227	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67910984	AATTGTCAGGAGAGT[G/T]CTCAAGTAGATGTGG	2186
rs745598250	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67865778	GAAGTCTTTAACTCC[A/G]TTAAAAGTGAATGGA	2186
rs745614838	snp	A/T	1.65206e-05	0.00287403	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67893434	AGGAAGTGATCATGA[A/T]AGGAAATATCAACAA	2186
rs745622491	snp	C/T			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67898039	TTAGACACCAATCTC[C/T]AATACTAGGAGATTA	2186
rs745653509	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67933486	AGATGGGAGGATTGC[G/T]TGAGCCCAGACATTG	2186
rs745666969	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67940366	AATACGTTCATGTGA[A/G]GTGTTGAATTATTTC	2186
rs745682264	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67864702	AGGTCAGTGAATACG[A/G]TATAGGTTGAGTATC	2186
rs745753527	in-del	-/TT			intron-variant	BPTF	GRCh38.p7	17:67886369	TTTTTCTTTTTTTTC[-/TT]TTTTTTGTGTGTGTG	2186
rs745791325	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67836224	GAGATTTGCTAAGAA[A/C]GTTATACTTAGACTT	2186
rs745793693	snp	C/T	1.92643e-05	0.00310351	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67826076	CGGACCACCGCGGCC[C/T]GGAGGGCCGTCAACA	2186
rs745794124	snp	A/G	4.94385e-05	0.0049716	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911659	CATTCATCAGTGCCT[A/G]AAAGTACCAATGACA	2186
rs745803582	snp	A/C/G	3.29958e-05	0.00406165	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67903898	ACATGGGTAAAATAC[A/C/G]CATTTCCAGTTAAGC	2186
rs745848177	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67874323	AAGTTGTTTCCAAAA[A/G]GGCCTCTGTTTTCTC	2186
rs745865381	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67885138	TTAGGTGATTTGAAG[A/C]GTATCTTGTCAGTGG	2186
rs745872402	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67934386	AGCTGGGTGTGATGG[C/T]GAGCACTTGTAATCC	2186
rs745886143	in-del	-/AGCC			intron-variant	BPTF	GRCh38.p7	17:67855154	GAAAATACAAAACTT[-/AGCC]AGGTGTGGTGGCGCA	2186
rs745908173	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67873778	ATTTATGACTACATT[G/T]TTTAGCTCTGTTGGC	2186
rs745921556	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67857364	ACGGGGTTTCACCGT[G/T]TTAGCCAGGATGGTC	2186
rs745923990	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67905280	GGGTGTGCTGGTACA[C/T]GCCTGTGATCCCAGC	2186
rs745927552	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67917851	GAGTCTCGCTCTGTC[A/G]CCTAGGCTGGAATGC	2186
rs745928228	snp	C/T	1.66999e-05	0.00288958	intron-variant	BPTF	GRCh38.p7	17:67924507	ATGCCAGATGCCTAA[C/T]AGGCTAGTTTCTGAT	2186
rs745936705	in-del	-/GG			intron-variant	BPTF	GRCh38.p7	17:67879041	CAGTCTTTAGTATCA[-/GG]AATATTTTGTCAGTC	2186
rs745952180	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67872817	AAATATAGGAATTAA[A/G]GGCTGGGCACTGCTA	2186
rs745973277	snp	C/G	1.65367e-05	0.00287543	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67912405	GACCCTGCCATCAAC[C/G]AAAGAGTCTGACAGT	2186
rs745998280	snp	A/C	1.65488e-05	0.00287647	missense, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67886301	CATACACCTGTCTCT[A/C]TTCAGGAAGAGATAG	2186
rs746009060	in-del	-/G	1.65515e-05	0.00287671	frameshift-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67911083	GACTTCTTGAAAGGA[-/G]GAATTAAACAGTTTA	2186
rs746052057	snp	C/G	1.6615e-05	0.00288223	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912514	TCAGAAGTTAAGAAA[C/G]TTACTTCATCACCTA	2186
rs746075722	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67844648	TCAGGCAATCTGCCC[A/G]TCTCGGCCTCCCAAA	2186
rs746098832	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67927984	TGCCGCCTGGGTTCA[A/G]GCAATTCTTCTGCCT	2186
rs746120747	snp	A/G	1.71449e-05	0.00292782	intron-variant	BPTF	GRCh38.p7	17:67866426	GATAAGTGGCATTAT[A/G]TCTAACATATAAAGT	2186
rs746138664	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67859484	ATCTTATAGATAAAG[A/G]GACTAAATCTCAAAG	2186
rs746163685	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67892270	AAATGGCTGATACAC[G/T]TTCTTACTACATGAA	2186
rs746184870	in-del	-/A			intron-variant	BPTF	GRCh38.p7	17:67837181	ATATTGATTTGCCTT[-/A]AAAAAAACTAGTCCT	2186
rs746205715	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67880481	TTTTATTTTTAAATG[C/T]ATGACCAGAACACAA	2186
rs746220306	snp	G/T			synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67912339	CTCCGAAACAAAATC[G/T]CATTTGCTGAGTTCT	2186
rs746228986	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67931002	CCGGATGCGGTGGCT[C/T]ACACCTGTAATCCCA	2186
rs746236314	snp	A/C	3.39092e-05	0.00411746	intron-variant	BPTF	GRCh38.p7	17:67931887	TAAAGCATTTTAATT[A/C]ATTGTTCTTTGTGTC	2186
rs746243081	snp	C/G	0.00110803	0.0235115	intron-variant, synonymous-codon	BPTF	GRCh38.p7	17:67929092	AAACAGCAAGATTGT[C/G]GCTGTAAATGTGCCA	2186
rs746265779	snp	C/T	1.64798e-05	0.00287047	synonymous-codon	BPTF	GRCh38.p7	17:67931994	AGGAAAGGCAATTAT[C/T]CGAACACCTGTGATG	2186
rs746288395	snp	G/T	1.65699e-05	0.00287831	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911450	CCATTGAAAATGACA[G/T]AGAAGAAAAAGTCTC	2186
rs746310194	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67913786	AGGTTTAGGGGATGC[A/G]TCCTAAATAGATAGT	2186
rs746355413	snp	A/G	3.58699e-05	0.00423482	intron-variant	BPTF	GRCh38.p7	17:67875058	AAGAAATATTTCATT[A/G]GTGTTATTTATGAAA	2186
rs746360984	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67902304	AATGGCCCAGTTGCC[A/G]TGCTGGACCTGGCCT	2186
rs746362525	in-del	-/TG			intron-variant	BPTF	GRCh38.p7	17:67908098	TAGAAACCACTGATA[-/TG]TGGGCTTTCTGGAAT	2186
rs746386939	snp	C/T	0.000181862	0.00953403	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911933	GTGAGGACAGGCTGC[C/T]GGTCAAGGGGACTGA	2186
rs746394009	snp	C/T	0.000380867	0.0137945	synonymous-codon, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67875608	AGCAAATCTTGGCGA[C/T]AACACAACAAATGCA	2186
rs746397866	snp	A/G	1.66804e-05	0.00288789	intron-variant	BPTF	GRCh38.p7	17:67919995	TTGGTTATTAATACT[A/G]TTGAATTAAATCACC	2186
rs746405075	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67975028	TCCTGAAGCTATCTA[A/G]GGAATTCCAACCACC	2186
rs746454221	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67953179	TGTTAGCCAGGATGG[G/T]CTCGATCTCCTGACC	2186
rs746459334	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67864956	ACGACAGGCGCCTGC[C/T]ACCATGCCCGGCTAA	2186
rs746464295	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67924878	CTCAGCCTCCCTAGT[A/G]GTTGAGACTACAGGC	2186
rs746531247	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67878310	TTGGTGGTTATTTTA[A/G]TGATTTTTGGTTTGG	2186
rs746533470	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67891635	TTTTTTGTGGAATAA[C/T]AGATGACTCACAGTA	2186
rs746577523	snp	A/G	0.00107354	0.0231434	intron-variant, missense	BPTF	GRCh38.p7	17:67929100	AGATTGTCGCTGTAA[A/G]TGTGCCAGCAACACA	2186
rs746587632	snp	A/G	1.65004e-05	0.00287227	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67910999	TCTCAAGTAGATGTG[A/G]TCAATGTTAGTGAGG	2186
rs746601439	snp	A/G	1.64765e-05	0.00287019	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67929389	CCATCAAGTACAGGT[A/G]CCAGTCAGCAAACCT	2186
rs746623049	snp	C/T	1.65897e-05	0.00288003	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67912813	CTCCACAGGCGGCAG[C/T]GTGGACATCATCTCT	2186
rs746640626	snp	A/G	0.000214559	0.0103554	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67893449	AAGGAAATATCAACA[A/G]TTATTTTAAATTGGG	2186
rs746660578	snp	A/T	1.72713e-05	0.0029386	intron-variant	BPTF	GRCh38.p7	17:67866734	TTAAGTCTGAGCTAA[A/T]CCGTTGGTATGAAAT	2186
rs746673648	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67851103	CCTGGGCTCCAGAGT[C/T]GGCCACTTATCTGTG	2186
rs746676304	snp	G/T	1.65247e-05	0.00287438	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67912918	TACATCTATGACTGT[G/T]AGCAAAGAGTATTCC	2186
rs746684958	in-del	-/TAAA			intron-variant	BPTF	GRCh38.p7	17:67921530	GACTCCATTTCCAAG[-/TAAA]TAAATAAATAAATAA	2186
rs746693483	snp	A/G	3.31961e-05	0.00407394	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67893605	CAGCAGGAGAGTTCA[A/G]ATGGAACGGTTCTGT	2186
rs746703746	in-del	-/A			intron-variant	BPTF	GRCh38.p7	17:67860073	CTATGGTCGTCATTC[-/A]AATTGCCTTTTTTGA	2186
rs746719809	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67852578	TAACACATAGGAATT[A/T]TACCACTACTGAATT	2186
rs746720597	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67865910	AACTCCTTCAAAAAC[C/G]AGAACTTAGCAAAGC	2186
rs746744970	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67836392	ATGTTCATAGTGCCT[C/T]TTTTGAGGTCTGTGT	2186
rs746746286	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67886589	CATACTCCCCTCCCC[A/G]AAGGTAACCACCATG	2186
rs746763967	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67934557	GATATTAGATATTAT[A/G]CTAATAATCTTAACT	2186
rs746780034	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67867158	CAAGAGAACCTTGTT[C/G]ATTCCACTGTAAATT	2186
rs746813408	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67935972	AAATATTGTGCTTAT[A/G]AATTGAATGTCTCAA	2186
rs746822320	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67899874	CAGTTTGGGATGCAC[A/G]CACATAGGTTCTAAA	2186
rs746870552	snp	C/T	3.29571e-05	0.00405924	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911690	GAGATGCCACACCTC[C/T]GTCAAGAGCAATGGA	2186
rs746888125	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67829209	TCATTGCAAGAGTTA[C/T]TTTGTTTTTGAGTTG	2186
rs746898153	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67924533	CTGATAAGTTTCTCC[-/T]TTTTTTCCTGCAGAG	2186
rs746903139	snp	A/G	1.64798e-05	0.00287047	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911776	TCTGATACCGTGTCT[A/G]TTCAGGATAGCAGTG	2186
rs746915773	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67940033	CCAGATTCTTTATAT[G/T]TTGTTTAAAATTCAT	2186
rs746930036	snp	A/G	9.595e-05	0.00692573	intron-variant	BPTF	GRCh38.p7	17:67909563	ATAACGTAAATTATC[A/G]TTACATGGTTCTTTT	2186
rs746938280	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67868603	AGTTTTAGCTTAGAT[A/G]AAATTATTAGGTAAG	2186
rs746941259	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67877184	ACGGAGATGTATCAG[-/T]TGACCAAAATAGATA	2186
rs746951154	in-del	-/TTC	1.64857e-05	0.00287099	cds-indel, nc-transcript-variant	BPTF	GRCh38.p7	17:67911621	AAGTGACACCATTGT[-/TTC]TTCTTCTTCCAAGAG	2186
rs746951735	snp	A/G	1.6554e-05	0.00287693	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67826269	AGGAGATGGAAGACG[A/G]CGACGACGACGCCAG	2186
rs746966175	in-del	-/TGT			intron-variant	BPTF	GRCh38.p7	17:67840460	TGCTGCTGCTCCTCT[-/TGT]TGTTGTTGTTGCTGC	2186
rs746993431	snp	A/G	3.41676e-05	0.00413311	intron-variant	BPTF	GRCh38.p7	17:67866439	ATGTCTAACATATAA[A/G]GTATTTCCCCCCATT	2186
rs746994814	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67968705	AGGCAGGAGAATGAC[A/G]TGAACCCGGGAGGTG	2186
rs747010868	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67919622	CAGAAGGGAAGGTTC[A/G]GATTATAAAGTGAGT	2186
rs747020481	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67880903	CCAACATTTAATTAA[C/T]GTTGATAAATGTTCC	2186
rs747039793	in-del	-/C			intron-variant	BPTF	GRCh38.p7	17:67838761	GATTACAGGCGTGAG[-/C]CACCACACCCAGCAC	2186
rs747045786	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67860854	GCGTGGACCACCACA[C/T]GCCTTTAAACAGCAT	2186
rs747073852	snp	A/C/G	3.2954e-05	0.00405908	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67928470	TGGCCCCCATAAGTG[A/C/G]CTCAGTTACAACTGG	2186
rs747073968	snp	A/G	4.98782e-05	0.00499366	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912529	GTTACTTCATCACCT[A/G]TTACTTCTGAAGAGG	2186
rs747101853	snp	C/T	3.30743e-05	0.00406645	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911365	ACCACAAACAAACTT[C/T]ATCCAAAAGATCGAG	2186
rs747111869	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67875166	TACCGTCCCCTCTTA[C/T]AACGTGTGTAACAAT	2186
rs747140169	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67906429	TAATGAGCTTTAGTA[C/T]TTAGAATCACCGAAC	2186
rs747166503	snp	A/T	1.64844e-05	0.00287087	missense	BPTF	GRCh38.p7	17:67932007	ATTCGAACACCTGTG[A/T]TGGTACAGCCAGGTA	2186
rs747215543	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67846849	GGGATTACAGGCACA[C/T]GTCACCACACCCAGC	2186
rs747223069	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67883790	ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT	2186
rs747242554	snp	A/C	1.64808e-05	0.00287057	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67866602	AGAAGAAATGCGTGA[A/C]GAAATCCACCGACAC	2186
rs747249126	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67929209	CTGATTTCAGTCCTC[A/G]GATCTCACATTCTAT	2186
rs747262820	snp	A/G	1.65165e-05	0.00287367	intron-variant	BPTF	GRCh38.p7	17:67894195	AGCCTTGTAAATGAT[A/G]AGTATTGGACTCCCT	2186
rs747274574	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67845341	TTGAATCAGTTACAC[C/T]TCTGATTGCAAATGG	2186
rs747291985	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67832820	TGAGGCAGAGTCTCG[C/T]TCTGTCACCTGGGCT	2186
rs747297847	snp	A/C	0.00341296	0.0411683	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67825978	CGCCGCCGGCCCCCC[A/C]CAGCACCAGCGCCCC	2186
rs747299865	snp	C/T			utr-variant-3-prime	BPTF	GRCh38.p7	17:67982629	AATGCCACGTCTGCT[C/T]TTCAGTGAAGAAGCT	2186
rs747300574	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67880666	GTGTAAGACAGGGTC[C/T]TGCTCTGTTACCCAG	2186
rs747316190	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67847673	GAGCCAGACTCCGTC[-/T]CAAAAAAAAAAAAAA	2186
rs747330309	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67833088	AGGCGTGAGCCACTG[C/T]GCCCCGCCTGATTTG	2186
rs747341222	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67960676	TACTTTTTACAGGAC[C/G]AAAAAGTCTGATTGT	2186
rs747363010	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67931333	GAATGATTAGCCGGA[C/T]ATGGTGCCATTCACC	2186
rs747378884	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67924276	ACTGTGCCCAGCTCC[A/G]ACTAACTTTTGTATT	2186
rs747382245	snp	A/C	1.64787e-05	0.00287038	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67920054	CAACAGAAATAATTA[A/C]GAGGAGAGATGTTGG	2186
rs747392396	snp	C/T	1.662e-05	0.00288266	stop-gained, nc-transcript-variant	BPTF	GRCh38.p7	17:67903853	AAAAAAGAGAAGAAA[C/T]AGGAAGAAGAAGAAA	2186
rs747419283	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67857437	AGTGCTGGGATTACA[C/G]GTGTGAGCCACCGTG	2186
rs747435319	snp	C/G	1.66994e-05	0.00288953	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912143	AAATATATTTGAAAG[C/G]TGAATGCTTGAAAGA	2186
rs747446474	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67902633	ATGAGCTGTCAGCCT[A/G]GGGGAGACTGTATTC	2186
rs747491705	snp	C/G	1.75656e-05	0.00296353	synonymous-codon, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67875728	GGTGGCATCTGAGCT[C/G]CCCCAGGATGTGCCA	2186
rs747491929	snp	C/G	3.29457e-05	0.00405854	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67854088	TTACGAGGTACTGCG[C/G]AACTTTGGCACTGTT	2186
rs747534019	snp	G/T	2.35735e-05	0.0034331	intron-variant	BPTF	GRCh38.p7	17:67910852	GAGTAAAAATTACAT[G/T]TATATAAATGTCTTT	2186
rs747545142	snp	C/G	1.64727e-05	0.00286986	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67854251	ACCTTTGGACCTGCT[C/G]ATCTGAAAGATAGCG	2186
rs747601765	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67855104	TTGAGAGTTCGAGAC[C/T]AGCCTGGCCAATATG	2186
rs747606156	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67851345	TCTGAAACAGTGCTG[A/G]ATGAACGCCTCAAGG	2186
rs747648833	in-del	-/AGT			intron-variant	BPTF	GRCh38.p7	17:67876366	GACGACTTCCATTTG[-/AGT]ACTGGTCAGCAGTGA	2186
rs747665499	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67866059	CTAGGAGTCTGAGTA[C/T]GCAGTGAACCACGAT	2186
rs747672375	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67872482	ACTTTGAGACAGGTG[A/G]ATCACCTGAGGTCAG	2186
rs747691047	snp	A/G	1.6483e-05	0.00287076	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67929422	ACTTCATTCCAGCCC[A/G]GGACAGCAACAGTCA	2186
rs747712890	snp	C/G	3.92488e-05	0.00442977	intron-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67929517	AGACTTATTTGGTTT[C/G]ATGTGTTGAGCACAT	2186
rs747714059	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67899275	AGTACAGAGCCAGCC[A/G]CTTTGGATGCTTGGC	2186
rs747744057	snp	C/T	1.65203e-05	0.002874	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912932	TGAGCAAAGAGTATT[C/T]CACACGAGACAAAGT	2186
rs747752511	snp	C/T	3.32873e-05	0.00407953	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67893630	TTCTGTCCATGGGTC[C/T]AAAGTTCTTACCATA	2186
rs747769948	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67847332	CCAGCCTGGCCAACA[C/T]GGTGAAACCCCATCT	2186
rs747778763	snp	A/C	6.63196e-05	0.00575807	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67874870	ATTGATAATGTTAAA[A/C]GCCCAGAAGAAACAG	2186
rs747783727	snp	C/T	3.29451e-05	0.00405851	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67854172	AGAGCAGTGCACACT[C/T]ATGGCAGAGATGCAT	2186
rs747800771	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67950676	AACCCCATCTCTACT[A/G]AAAATACAAAAAAAT	2186
rs747823837	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67837905	TTGAGAGTTTCCTGG[A/C]CAAGTGGTGGAAAGT	2186
rs747831006	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67838962	CCTATTCTTTTTTCT[A/T]ATTGTTTCTTGTAGC	2186
rs747831779	snp	A/G	3.31252e-05	0.00406958	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67826280	GACGACGACGACGAC[A/G]CCAGTTACTGCACGG	2186
rs747833604	in-del	-/CT/CTC			intron-variant	BPTF	GRCh38.p7	17:67909279	AGGTCCCCCCCCCCC[-/CT/CTC]TTTTTTTTTTTATCC	2186
rs747836857	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67852713	ATTAAATATTTTGTA[C/T]TTAAATGAATGTGTG	2186
rs747852175	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67948577	AACTCTGAGAAGAGC[C/T]TTTCATGTCTATGAC	2186
rs747857841	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67936894	AGTAATTTCCCAAGC[A/T]ATTAATCTGGGATTC	2186
rs747874385	snp	A/G			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67886777	TTTTTTTACTCAGTG[A/G]TACATGGAGAGAATC	2186
rs747900099	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67919738	GTGCTTGCTGCTTCT[C/G]TCCTAGGCTTTTTAT	2186
rs747903509	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67901498	AAAGTCAAAAGACAG[A/G]TGACAAACCGAGGAA	2186
rs747915677	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67875369	CATTCTTAATATATT[A/C]TTAAATATTCTTAAA	2186
rs747951855	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67921076	CAAAAATATTGGTAA[A/T]GTGCATGCCTGTAAT	2186
rs747973227	snp	C/G			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67888021	CTACGATTGATGCCT[C/G]CAGCAAAAGTTGGGT	2186
rs747989841	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67916302	AACTGAATGCTGTCA[A/G]TAGAAAGCATTGTCT	2186
rs748004955	snp	C/T	0.000347149	0.0131702	intron-variant	BPTF	GRCh38.p7	17:67909578	GTTACATGGTTCTTT[C/T]TAGCCAAAAATAATA	2186
rs748023574	in-del	-/TT			intron-variant	BPTF	GRCh38.p7	17:67966420	CTCATCTTAGGTAAC[-/TT]TATTACTAGAGCAGA	2186
rs748032435	snp	A/G	3.32745e-05	0.00407875	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67928363	TTTTTAGAAACGACT[A/G]GAGCAGCAGAAGCCG	2186
rs748043318	snp	A/G	1.65002e-05	0.00287225	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911885	TGGAGCCGTTAAAGT[A/G]TGAGTTGGTTTCTGG	2186
rs748070528	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67845514	ATGGTGGTTCACGCT[A/T]GTAATCCTAGCACTT	2186
rs748086072	snp	A/G	1.65614e-05	0.00287757	synonymous-codon, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67886306	ACCTGTCTCTATTCA[A/G]GAAGAGATAGGTAAG	2186
rs748105125	snp	G/T	1.65578e-05	0.00287726	missense, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67891901	AATCTCCTGGAGCTG[G/T]AAAAGGAGCATCTGG	2186
rs748123787	snp	C/T	0.00123993	0.0248682	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67826060	CGGCGGCCACCTGGC[C/T]CGGACCACCGCGGCC	2186
rs748144320	snp	A/G			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67897066	GGCATGGTGGCTCAT[A/G]CCTGTAATCCCAGCA	2186
rs748164430	in-del	-/ATTTTTAATTTTTTTAC			intron-variant	BPTF	GRCh38.p7	17:67898459	TTATTGGGTTTTTTT[-/ATTTTTAATTTTTTTAC]ATTTTTAATTTTTTC	2186
rs748185181	in-del	-/GTA			intron-variant	BPTF	GRCh38.p7	17:67935886	TGTATAGGTATCCTT[-/GTA]GTAAGACTTTCAGAA	2186
rs748264645	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67838240	CTGTGGCTGGCCATA[A/G]TTTATTCACCCCATT	2186
rs748268059	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67968474	TAATAATACAAGTTA[A/G]TGGTAGAAAATTCAT	2186
rs748344080	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67834991	GCTGAGGTGGGAAGA[C/T]CACTTAAGGCAGCAG	2186
rs748379517	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67883900	CACCGCGCCCGGCTC[A/G]TTTTGTTTTTTATAA	2186
rs748401171	snp	A/G	5.247e-05	0.00512174	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67826175	GAGGAGGAGGACGGC[A/G]ACGCCGAGGAGACCC	2186
rs748412586	snp	C/T	1.64958e-05	0.00287187	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67904726	CAAAAAGGTGAAGAG[C/T]ACAGAGTGACAGGAT	2186
rs748420257	snp	A/G			missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67854045	ATTTAATGGTGCCTA[A/G]TGAGCATATAATGAA	2186
rs748439389	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67932977	AAAAGATCAGCCAGG[C/T]GCAGTTGCTCATGCC	2186
rs748471736	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67855961	AGTTTTACAGTGATA[C/T]GCCCTTGTGTGGGCT	2186
rs748480512	snp	C/T	1.64727e-05	0.00286986	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67854286	TTCCACACTGTATTT[C/T]ATAGATGGGATGACG	2186
rs748489719	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67902772	ACTGAAATCCCCTCC[C/T]ACATCTTTTCGGCAT	2186
rs748500920	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67872595	CCTATAGTCTCAGCT[A/G]CTTGGGAGGCTGAGG	2186
rs748501630	snp	A/C/G	0.000125155	0.00790979	intron-variant	BPTF	GRCh38.p7	17:67922805	TTAATTTTAGAAGCA[A/C/G]TATTGCTTAAAATAT	2186
rs748521559	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67903667	AGTTTTGTCAGTTGG[A/G]GTTGTCTGGTTTGTA	2186
rs748531443	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67871732	TATGCATATTTAGTA[C/T]AGATCAGATACAATG	2186
rs748546485	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67955024	GCCGGGTACGGTGGC[C/T]CATGCCTGTAATCCT	2186
rs748550475	in-del	-/TTTTTTCTT	1.8851e-05	0.00307004	intron-variant	BPTF	GRCh38.p7	17:67886353	TCCTTTAAAGGGAAG[-/TTTTTTCTT]TTTTTTCTTTTTTTT	2186
rs748555106	snp	A/G	1.65113e-05	0.00287322	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911032	TTTCATCTAAGGACT[A/G]GTTACAAAAAGAAAA	2186
rs748556608	snp	A/C	1.67321e-05	0.00289236	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67912276	ATCTGCTATAAGGCC[A/C]TTCATTAATGGTGAT	2186
rs748570144	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67880588	GTGATGAAGTATATT[G/T]CTTAATATTCAAACA	2186
rs748608461	snp	A/G	1.64836e-05	0.0028708	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67893471	TAAATTGGGTCAAGA[A/G]GGGAAGTATCGCGTC	2186
rs748655526	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67939610	GGGCCAGGTGAGGTT[C/G]CTCATGCCTGTAATC	2186
rs748686993	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67938751	AATTTTTAAAAAGAC[C/T]AGTCTGGCCGCATTT	2186
rs748701027	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67857225	CGAGTGCAATGGCGT[G/T]ATCTCGGCTTACTGC	2186
rs748716691	snp	A/G			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67888451	AAATACTAGCCGGGC[A/G]TGGTGGTGTGTGCCT	2186
rs748720281	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67890686	AGGGAAGTATCTCCC[C/T]AAAGGAAAGAAGGGG	2186
rs748727775	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67840323	TGTTGCCCAGACTGA[C/T]TTCAAACTCCTGGGC	2186
rs748737505	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67869319	CTGTGTGTTAGATTA[C/T]GTATACAGTATAATC	2186
rs748751717	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67868497	ATTCAAGGGTTCTGC[A/C]TCCTGAGAATACTGT	2186
rs748768776	snp	A/C/G/T	5.16831e-05	0.00508326	intron-variant	BPTF	GRCh38.p7	17:67875039	AAAAAATTACTTGAT[A/C/G/T]AAAAAGAAATATTTC	2186
rs748790606	snp	A/G	1.64784e-05	0.00287035	synonymous-codon	BPTF	GRCh38.p7	17:67931970	AACACCACTCCAACA[A/G]TCAACACTAGGAAAG	2186
rs748796958	snp	C/G	1.75826e-05	0.00296496	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67913181	CGACCTTTGGCATCA[C/G]TTGGAGGTATGTACT	2186
rs748805416	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67902611	CAGTTGAGTGCAGTT[A/G]ATAGGCATGAGCTGT	2186
rs748810429	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67926670	GCTTATTTATGAATA[C/T]AGCTAACACTTCAAC	2186
rs748844175	snp	A/G	1.64732e-05	0.0028699	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67918768	CCTGATGTTACGGTT[A/G]CTGTGGGCAAGTTTG	2186
rs748882201	snp	C/T	3.3173e-05	0.00407252	synonymous-codon, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67875605	GTCAGCAAATCTTGG[C/T]GACAACACAACAAAT	2186
rs748896813	snp	G/T	3.33684e-05	0.00408449	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67909739	AATGGATATCTCAAA[G/T]ATTACTGAGAAGAAG	2186
rs748939899	snp	A/G	1.7475e-05	0.00295588	intron-variant	BPTF	GRCh38.p7	17:67853916	ATGTATTGATTTGTA[A/G]TGATGTCACGTCTTT	2186
rs748981904	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67839323	TTCTCTTTTTTTTCC[G/T]AAGTTTTTTTTTAAA	2186
rs748993040	snp	A/G	1.6473e-05	0.00286988	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67854051	TGGTGCCTAATGAGC[A/G]TATAATGAATGTCAT	2186
rs749015297	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67908980	GCTGAGATCACAGGT[A/G]TGCACCACCACACCC	2186
rs749023020	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67909268	AGCCACCGCACCAGG[G/T]CCCCCCCCCCCTTTT	2186
rs749026452	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67921357	TAGCAAAACCCCATC[A/T]CTACTAAAAATACAA	2186
rs749028415	snp	G/T			intron-variant, utr-variant-5-prime	BPTF	GRCh38.p7	17:67889243	CTCAGTTTAGTTCTT[G/T]TTCTCCATTCCTTTA	2186
rs749040447	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67846779	AGTCTGGGCTCACTG[C/T]AACCTCTGCCCTTTG	2186
rs749042101	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67862521	ACAAAGTGGTGGGAT[C/T]GGGATTTGAACCTAG	2186
rs749102369	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67876336	AGGATTTTGACAACC[C/T]GCAGTTCTTATGGGG	2186
rs749139786	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67907575	TGGCCAGGCTGATCT[C/T]GAACTCCTGACTTCA	2186
rs749148609	snp	A/G	3.30863e-05	0.00406719	missense, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67891915	GGAAAAGGAGCATCT[A/G]GCTCAACTCGAATCA	2186
rs749160366	snp	A/G	4.94262e-05	0.00497098	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67928481	AGTGGCTCAGTTACA[A/G]CTGGAACCAAAATGG	2186
rs749164289	snp	A/G	3.50564e-05	0.00418652	intron-variant	BPTF	GRCh38.p7	17:67909809	GGGTGATAAGAATGC[A/G]CTGGATCAGGGTCCC	2186
rs749195514	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67915563	CCTTCATCTCTTTCT[A/G]TACCTCTACACCCCT	2186
rs749199168	snp	A/C/T	3.32769e-05	0.00407892	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912761	CAAAATCCACTGTCA[A/C/T]AACCACCACTACAAC	2186
rs749203528	snp	G/T	1.95406e-05	0.00312569	intron-variant	BPTF	GRCh38.p7	17:67892062	TGTTTAAAACAAAAA[G/T]CTGTGGAATGTGAGA	2186
rs749216087	snp	G/T			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67886730	TTGAAATATAAACAG[G/T]ATCATTCTGCATGTA	2186
rs749232290	in-del	-/C			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67896488	CCCAGTGCACATAGA[-/C]CCCCTTGAATCTAAA	2186
rs749235670	snp	A/G	8.23961e-05	0.00641804	missense	BPTF	GRCh38.p7	17:67931941	CAGATTCGCCCTGGT[A/G]TGACCGTGATTAGAA	2186
rs749253326	snp	A/C/G	3.31253e-05	0.00406962	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911516	GTAAAACAAAAGGAA[A/C/G]TGATTTTTTCATCGA	2186
rs749255005	snp	A/G	1.64781e-05	0.00287033	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67866622	TCCACCGACACATGG[A/G]CATAACTGAAGACCT	2186
rs749305717	snp	A/G	1.66535e-05	0.00288556	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67826266	CGGAGGAGATGGAAG[A/G]CGACGACGACGACGC	2186
rs749348906	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67933402	TAGGGAGACCCCATC[G/T]CTACAAAAAATAAAA	2186
rs749350736	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67871831	TTGTTGTTTGTTTTG[A/T]TTTTGTTTTTTTGAG	2186
rs749373721	snp	C/T	0.000370367	0.0136032	intron-variant	BPTF	GRCh38.p7	17:67922813	AGAAGCAATATTGCT[C/T]AAAATATTCTGATTT	2186
rs749380767	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67964770	CTTTGGGAGGCCAAG[C/G]TGGGCGGATCACAAG	2186
rs749387165	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67883998	AGTATTGTTCTACAC[C/T]TTGCTTTTAACATTT	2186
rs749387196	snp	C/T			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67897887	AATAGAAAATTATGG[C/T]CCTGTCTTCTTTATT	2186
rs749392664	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67916697	CTTGAACCTGGGAGG[C/T]GAAGGTTTCAGTGAG	2186
rs749412697	in-del	-/AATATGGATGAA	1.77203e-05	0.00297655	cds-indel, nc-transcript-variant	BPTF	GRCh38.p7	17:67909590	TTTTTAGCCAAAAAT[-/AATATGGATGAA]AATATGGATGAGTCA	2186
rs749469071	snp	C/T	0.000183644	0.00958062	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67912297	TAATGGTGATGTCAT[C/T]ATGGAAGATTTTAAT	2186
rs749481908	snp	C/T	6.63449e-05	0.00575917	intron-variant	BPTF	GRCh38.p7	17:67923018	TTAATACCTGGTCAG[C/T]TATTTGAAGATTTTA	2186
rs749491690	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67900376	TCCCAAAGTGCTGGG[A/C]TTACAGGCGTTAGCC	2186
rs749502996	snp	A/G	1.64923e-05	0.00287156	missense, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67886172	AACACTAGTGCTACC[A/G]CTACCTCCATCCAGC	2186
rs749504820	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67835960	GTGAGCCACCATGCC[C/T]GGCCCAGTCCTGGTA	2186
rs749522015	snp	A/G	1.65471e-05	0.00287633	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912391	CGAGATAGCCTTGAG[A/G]CCCTGCCATCAACCA	2186
rs749523063	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67872671	AGATCACGCCACTGC[A/C]CTCCAGCCTGGGCAA	2186
rs749545380	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67877429	TCAGTGGATGAGATG[C/T]CTTGTTAGAAGAATT	2186
rs749556331	snp	A/G	1.65173e-05	0.00287374	missense, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67886287	GAGAAAGAGAATCTC[A/G]TACACCTGTCTCTAT	2186
rs749559945	snp	A/G	1.64803e-05	0.00287052	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67854681	CTGAAATCCAAAAAA[A/G]TAAACCATATATTCG	2186
rs749561491	in-del	-/GTG			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67898186	ACCAGCATGGCCAAT[-/GTG]GTGAAACCCCATCTC	2186
rs749608240	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67859218	TGGCATGATCATGGC[A/T]CACTGCAGCGTCAGT	2186
rs749631893	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67902525	GCTCCCAGTGAGGAT[C/T]TGCTCCCTTTCCCCT	2186
rs749639875	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67890915	AAGGAAAAATCAGAG[C/T]TTATTCAACTATCTG	2186
rs749670637	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67925148	AGCTGTGGTTTTGTA[A/C]AAAGTATACATATTT	2186
rs749679786	in-del	AATAGTGTTCTCTTTTTTCCATT/GCAGAGTCTCGCTCTGTCAGCTAGGCTGGAG			intron-variant	BPTF	GRCh38.p7	17:67923504	TTTTTTTTTTTTGAA[lengthTooLong]TGCAGTGGCATGATC	2186
rs749692430	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67905081	TTTTTAGAAGACGCC[C/T]CAGCCGCCTGATTAT	2186
rs749716101	snp	C/T	9.95223e-05	0.00705346	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912485	ATCAGGTAGAAGATA[C/T]GGAAATAGAAACCTC	2186
rs749720186	snp	A/G	1.67119e-05	0.00289062	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911194	TCAAAAAATCTCTCT[A/G]AATCACCAGTAATAA	2186
rs749735590	snp	C/G	1.66693e-05	0.00288693	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67893652	CTTACCATATCTACT[C/G]TGAGACTGACTATCA	2186
rs749771654	snp	A/T	1.656e-05	0.00287745	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67911328	TGATTCCTCAGTTCT[A/T]AGAATGAGTGATCCT	2186
rs749779537	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67851032	AGGGAAAAGAGGTAT[A/G]TATATTTACACTCAC	2186
rs749786506	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67830077	TTAAATTTAGACTTA[C/T]TTCAGCCTATAGGTT	2186
rs749787096	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67880403	TTTGTTTTTTTATGA[C/T]GTCTACTATCAAGGC	2186
rs749830426	snp	A/C	1.65578e-05	0.00287726	intron-variant	BPTF	GRCh38.p7	17:67894002	AAGGTCAACCTAGTG[A/C]AATAATTTCTCTCAT	2186
rs749852337	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67927041	TATTCAGGTATATAG[G/T]ATAGGTACAAAAGTA	2186
rs749866753	snp	A/G	5.02736e-05	0.00501341	missense, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67875699	CCCGATAGCAGCAAC[A/G]TGGCAGAGAAGAAGG	2186
rs749868600	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67879419	TGCTGGGATTAGAGG[C/T]GTGAGCCACCGCGCC	2186
rs749870805	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67882417	AGATAGCATACTTAG[-/T]TTTCTTTGTTTACAT	2186
rs749881126	snp	G/T	1.65116e-05	0.00287324	intron-variant	BPTF	GRCh38.p7	17:67903948	AACCCTTTAAAATAG[G/T]GTTAGCCATTTCTGA	2186
rs749901542	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67904540	TGAAAACTAAATTGA[C/T]TAGTAAATTTTTTTT	2186
rs749914925	in-del	-/TATAAT			intron-variant	BPTF	GRCh38.p7	17:67832339	TAAAATGCACGTAAA[-/TATAAT]TATAATGTTTTAATT	2186
rs749929775	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67917358	TCAAACTCCTGACCT[C/G]GTGATCCCCCCACCT	2186
rs749960499	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67939391	GATGTTATTCAGTAG[A/T]TAGTAATGAGTCTGT	2186
rs749976806	in-del	-/CCA	1.67326e-05	0.00289241	cds-indel, nc-transcript-variant	BPTF	GRCh38.p7	17:67893707	CATCCTTTCTTCATC[-/CCA]ACTGGGCATCACATA	2186
rs749995986	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67893966	TGGAGGCCAAAGTTA[A/C]AACTATTGTGCTTTT	2186
rs750018730	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67842953	ACTTCAGAGATAAAG[A/G]GCAACAGAAATGGTA	2186
rs750061424	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67926418	CAAGCTCCGCCTCCC[A/G]GGTTCACGCCATTCT	2186
rs750069583	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67858090	CGTGCCCGGCTAACA[A/G]TATTTCTTTAGCATG	2186
rs750076483	snp	A/G	1.68323e-05	0.00290101	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912229	AATAAAATAATCCCT[A/G]AGAATGATATTAAAT	2186
rs750093355	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67858728	GAGCTCATAGTCATC[A/G]GGATGGCTGGGAACA	2186
rs750107058	snp	A/G	1.6563e-05	0.00287771	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912370	TCAGATGCTGAAGGT[A/G]ACTACCGAGATAGCC	2186
rs750130106	snp	A/C	1.64746e-05	0.00287002	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67854350	GATAAGGAGTACCAT[A/C]ACGTTCTTCCTTACC	2186
rs750131418	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67905688	CACTCGAGCCTGGAT[C/G]ACAGAACCAGACTCA	2186
rs750178794	snp	C/G			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67898172	CCCAGGAGTTTAAGA[C/G]CAGCATGGCCAATGT	2186
rs750186127	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67836355	ATTTTACTAGAAATA[C/T]GGCTTCTTGCTCGAT	2186
rs750217353	snp	C/G			missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911774	GTTCTGATACCGTGT[C/G]TATTCAGGATAGCAG	2186
rs750223081	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67892757	TTCAAAAGCTTTCTG[A/C]AATACTATTTTACTT	2186
rs750257709	snp	A/G	1.64762e-05	0.00287016	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67929381	GTATCATTCCATCAA[A/G]TACAGGTACCAGTCA	2186
rs750268511	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67928008	TCTGCCTCAGCCTCC[C/T]GAGTAGTTAGAATTA	2186
rs750300380	snp	C/G	1.65666e-05	0.00287802	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67893583	GCACATAAGTTCTGT[C/G]TGACTCCAGCAGGAG	2186
rs750305209	snp	G/T	1.66172e-05	0.00288242	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911139	AAAAATCAAGTTGGA[G/T]GGTGGAATTAAGGGT	2186
rs750310852	snp	A/G	1.67854e-05	0.00289697	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67929473	GGCTCTGGAGGAACC[A/G]CAAGCAATTCACAAG	2186
rs750322819	in-del	-/T			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67896804	CATGCAATTAAAGAC[-/T]TCCTAGGAGAAGTTG	2186
rs750327227	snp	A/G	0.00018474	0.00960917	synonymous-codon	BPTF	GRCh38.p7	17:67947773	TTTAAAACAGAAAAA[A/G]AGCATGACTCCAGCT	2186
rs750355395	snp	A/G	5.0145e-05	0.00500699	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67874836	AATTTTGGAATCCAT[A/G]AGAGCCAAAAAGGGA	2186
rs750358782	snp	A/G	1.66796e-05	0.00288782	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67911247	GAGTGACTCGATGAG[A/G]CAAGAACAGAGCCCA	2186
rs750362401	snp	A/T	1.67767e-05	0.00289622	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67913134	CAATGCAAAACCTGC[A/T]TTGGATATATGGCCA	2186
rs750371442	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67975447	GTTTGCATGTAAAAA[C/T]GCATTATACTTAGAT	2186
rs750372616	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67830771	GTATGCTGTGTTGGG[C/T]AGTACCTAGAGGATC	2186
rs750374995	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67852379	TTCCTGTCCCCCGAC[C/T]CTCCCCAGAAGCAAG	2186
rs750395606	in-del	-/A			intron-variant	BPTF	GRCh38.p7	17:67872847	AACGCCTGTAACCCC[-/A]GTGCTTTGGTAGGCC	2186
rs750437033	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67935878	AAGAATTTTGTATAG[A/G]TATCCTTGTAGTAAG	2186
rs750439201	in-del	-/A			intron-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67929966	ACAAAAAATACAGAA[-/A]TTAGCCAGGCGTGGT	2186
rs750448702	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67913190	GCATCACTTGGAGGT[A/G]TGTACTTTAAAATGT	2186
rs750466723	snp	C/T	1.65463e-05	0.00287626	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67853967	CAAGAGTACATCGGC[C/T]TCGTTCTCCTATATT	2186
rs750474702	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67902210	CACAACTGAGCACCC[C/T]GCCCAGCTTTGAGCT	2186
rs750481117	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67917594	AAAGGTCTTACTAGA[-/T]TTGTAAGATGTTTTT	2186
rs750518811	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67949959	TTAGGAGTCTGAGGT[A/G]GGGAGAATTGCTTGA	2186
rs750528143	in-del	-/TGT	1.65949e-05	0.00288048	intron-variant	BPTF	GRCh38.p7	17:67920178	CTTTCATGATTAACC[-/TGT]TGTTAACCATGTATT	2186
rs750559960	snp	A/G	3.34868e-05	0.00409173	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912019	AAATGTAGTGATCAA[A/G]TAAAGCTAAAAAATA	2186
rs750576908	snp	A/G	1.66117e-05	0.00288194	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67909680	GATTCTGAAAAAGAT[A/G]AGGTAAAAGGTTCAG	2186
rs750588856	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67920611	TAGAGCACCAGTACA[A/G]TAGGCACTGGGTGGC	2186
rs750626624	snp	A/C	1.6664e-05	0.00288647	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912632	AATCTAAAAGAAAAA[A/C]CGTCATCACAGAAGT	2186
rs750628103	snp	C/G			upstream-variant-2KB	BPTF	GRCh38.p7	17:67823648	CTTACCTGGTCCCTG[C/G]AGACATATACACATT	2186
rs750634465	snp	C/T	1.64779e-05	0.00287031	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67928452	CAGCACAGAAGGTTA[C/T]GGTGGCCCCCATAAG	2186
rs750637161	snp	C/T			upstream-variant-2KB	BPTF	GRCh38.p7	17:67825496	TGCGGCCGCTGTCGG[C/T]TCCCCCAGTCACCGA	2186
rs750637413	snp	A/G	4.78675e-05	0.00489198	intron-variant	BPTF	GRCh38.p7	17:67875783	CCTCTGTAATGGGGG[A/G]AATCCTTCCCTTTTG	2186
rs750639341	snp	C/T	5.04995e-05	0.00502466	synonymous-codon, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67892001	GGCAGCCGCTGCACA[C/T]GAAGCAAATAAATTA	2186
rs750641204	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67860757	AGAGACAGAGTCTCA[C/T]TATGTTGCCAGGCTG	2186
rs750678904	in-del	-/AAAAAAAAAAAAAAA			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67897342	GTGAAACTCTGTCTC[-/AAAAAAAAAAAAAAA]AAAAAAAAAAAAAAA	2186
rs750687823	snp	A/G	1.66996e-05	0.00288956	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67928586	ACATGGGTTAAGCAA[A/G]GCCAGTCAAATTCAG	2186
rs750698125	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67838729	AGTCCTTCCTCCTTG[A/G]CTTCCCAAACTGTTG	2186
rs750702855	snp	C/T			intron-variant, utr-variant-5-prime	BPTF	GRCh38.p7	17:67888878	GGGACTTCTATAGGA[C/T]TAAACAATCATATAA	2186
rs750733750	snp	G/T	1.67705e-05	0.00289568	missense, utr-variant-5-prime, nc-transcript-variant	BPTF	GRCh38.p7	17:67893392	TAGTTAACTCTCAAG[G/T]AGAAATTTCACGGTT	2186
rs750734356	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67921785	GCCTGTAATTCCAGC[G/T]CTTTGGGAGGCCAAG	2186
rs750746129	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67866211	AGTTGGTTGAGATGT[A/C]GCTGAAACTGGCTTC	2186
rs750759054	snp	G/T	3.29783e-05	0.00406055	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67866577	GGGAAGCAGAACTCT[G/T]CAAAATTCTAGAAGA	2186
rs750791154	in-del	-/AG			intron-variant	BPTF	GRCh38.p7	17:67864422	AATCCCAGCTTCTTC[-/AG]AGGCTGAGGCATGAG	2186
rs750868492	snp	A/G	1.66471e-05	0.00288501	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912718	AAAGGCGATAAGCAA[A/G]CTGTGGTTTCTTCCA	2186
rs750895633	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67868037	TGTTTATTTTTTCAG[A/G]CATTTATTTCTATGA	2186
rs750921871	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67848693	GTTCATCCGAACAGT[A/T]CAGAGAAGAGAACAT	2186
rs750928406	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67846589	TCTCCCACCTGCACA[A/G]TAGGCACTTGTTATT	2186
rs750957213	snp	C/T	0.000225963	0.0106269	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	BPTF	GRCh38.p7	17:67825580	GCAATTCGGATTGAG[C/T]CTTCTCCCTCCACCC	2186
rs750962156	snp	A/G	0.000186007	0.00964204	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67903828	AAGAGAAGAAAAGGA[A/G]AAAGTCAAAAAAAAA	2186
rs750969204	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67839281	TGTGGGTTTGAGACC[G/T]TCAATGTGTTGAATG	2186
rs751011017	in-del	-/A			intron-variant	BPTF	GRCh38.p7	17:67871442	TGAGACTTTGTCTCC[-/A]AAAAAAAAAAAAAAA	2186
rs751015516	snp	A/T	3.88742e-05	0.00440858	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67826158	TGGTCTCCGAGGAGG[A/T]GGAGGAGGAGGACGG	2186
rs751025077	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67879863	ACCCAACCCGAGAGC[A/G]TTAATCTGCTCTTGA	2186
rs751030598	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67981015	ATACAAAAAATTAGC[C/T]GGGCATGGTGGCATG	2186
rs751032007	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67893041	GTATATGTTATAAAC[C/T]TGAAAAAAATGATAG	2186
rs751039972	in-del	-/GAG	0.0150367	0.0853947	cds-indel, nc-transcript-variant	BPTF	GRCh38.p7	17:67826151	GAGGACATGGTCTCC[-/GAG]GAGGAGGAGGAGGAG	2186
rs751043697	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67843100	TAGATACATATATCT[A/C]TATATATGTAGATGT	2186
rs751045803	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67860281	GATTAAAATAATTTC[A/T]GTTTAACTGTACTTT	2186
rs751074391	in-del	-/C			intron-variant	BPTF	GRCh38.p7	17:67896053	ACTGCAGCTCCGCCT[-/C]CCGGGTTCACGCCAT	2186
rs751096700	snp	A/G	1.65564e-05	0.00287714	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912377	CTGAAGGTAACTACC[A/G]AGATAGCCTTGAGAC	2186
rs751137426	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67830822	TCCCCCTTTTCTGTA[G/T]AATAGGGATTGGGCT	2186
rs751150991	snp	A/T	1.64925e-05	0.00287158	intron-variant	BPTF	GRCh38.p7	17:67924612	AACAGAAGAAGGCAG[A/T]GGACATCAAGGCCCA	2186
rs751171899	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67867117	TGTGTGTATATTTTA[A/C]TTTAGTTCTCCATAT	2186
rs751206145	snp	A/G	1.65636e-05	0.00287776	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67912456	AGCATCTTGTCCAGA[A/G]AGCAATTCAGTTAAT	2186
rs751212184	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67881117	TAAAAAATGATAGGA[A/G]TGAGAACATAAGAAA	2186
rs751221134	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67894884	ACTTCAACAGATGAT[G/T]AAAAAGAAAGAAAAT	2186
rs751222148	in-del	-/A			intron-variant	BPTF	GRCh38.p7	17:67882528	GGGTATTCCTATCCT[-/A]ATGTGCATTAATAAT	2186
rs751239459	snp	C/T	4.95995e-05	0.00497969	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67928377	TGGAGCAGCAGAAGC[C/T]GACAGTGATTGCAAC	2186
rs751262818	snp	C/G	1.88379e-05	0.00306897	intron-variant	BPTF	GRCh38.p7	17:67854767	AGACTCATAATGTAA[C/G]TAAATCTGGTCTTAA	2186
rs751292289	in-del	-/GT			intron-variant	BPTF	GRCh38.p7	17:67830722	TTAGCAAGAGCCTGA[-/GT]GTGTGTGAATAGGAA	2186
rs751299959	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67868225	GGTATGCTGTGAAAA[A/G]TGAATCTCTCTCCTT	2186
rs751327336	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67860460	AAAAATATGTTATTT[A/G]TATAGATTAGTGAAG	2186
rs751343147	in-del	-/TTAA			intron-variant	BPTF	GRCh38.p7	17:67917621	TTTGGTTTAATTTAA[-/TTAA]TTAATTAATTAATTA	2186
rs751345481	in-del	-/GAGGAGGAGGAAGAGGAGGACATGGTCTCC	5.70077e-05	0.00533859	cds-indel, nc-transcript-variant	BPTF	GRCh38.p7	17:67826121	GACCACGAGAGCGAG[lengthTooLong]GAGGAGGAGGAGGAG	2186
rs751352098	snp	C/T	1.64795e-05	0.00287045	synonymous-codon	BPTF	GRCh38.p7	17:67931946	TCGCCCTGGTATGAC[C/T]GTGATTAGAACACCA	2186
rs751357403	snp	A/C	1.84021e-05	0.00303327	intron-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67929500	CAAGTAAGAATTCTT[A/C]CAGACTTATTTGGTT	2186
rs751368147	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67959272	GGAGGGACGCTCTTC[C/T]TAGCCACTTGGCTCA	2186
rs751368716	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67915156	AAGGCTGAGCAATAT[G/T]GGAAAACTTGTCTCA	2186
rs751368771	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67900922	ACTGAGCCTAGAAGT[C/T]GGAGGAGGATTGCTT	2186
rs751387581	in-del	-/A			intron-variant	BPTF	GRCh38.p7	17:67870001	GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA	2186
rs751425232	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67831995	CTCCTGGGTTCAAGC[A/G]ATTCTCCTGCCTCAG	2186
rs751472386	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67857466	TGCCTGGACAGCAGA[-/T]TTTTTTTTTTTTTTT	2186
rs751490762	snp	C/T	1.83363e-05	0.00302784	intron-variant	BPTF	GRCh38.p7	17:67826380	CTCCTTCCCCACCTC[C/T]TCTGCCCTCCCCCCT	2186
rs751506326	snp	A/C/T	0.00039599	0.0140657	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911876	TTGAAGTCTTGGAGC[A/C/T]GTTAAAGTGTGAGTT	2186
rs751538531	snp	C/G	1.6473e-05	0.00286988	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67894103	GGCTTTAGCCATTTT[C/G]GAGTGTGCAGTTAAA	2186
rs751541910	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67876105	TTCTGTAGATACTAA[C/T]AAATTAATTTTATGT	2186
rs751545655	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67834330	AGGTTTGTTTTGCAC[C/T]CCAAAATTTTGTCAG	2186
rs751555733	snp	A/G	1.78797e-05	0.0029899	intron-variant	BPTF	GRCh38.p7	17:67875540	CTTTGAAGTTTTGTT[A/G]TGCATTTTGCTGTAG	2186
rs751559625	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67936786	TGCCAGGGTGTATGT[A/G]TTTTGTACATAAGCA	2186
rs751572182	snp	A/G	1.75795e-05	0.0029647	missense, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67892027	AATTATTTAAGGAGG[A/G]CAAAGAGGTGTGTTC	2186
rs751578544	snp	C/T	1.66671e-05	0.00288674	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67910914	TGACAGTGATAAACC[C/T]TGCAAGGAAGAACCA	2186
rs751604203	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67902331	GCCTTTCAGAGGTGT[A/G]TAGAAGCCAAGCCCT	2186
rs751608744	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67938087	CTCAGCCTGGGCAAT[A/G]GAGCGAGACTTCACA	2186
rs751610967	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67920730	CAGTAAGCTAAGAGA[A/G]TAATATTGGAAAAGA	2186
rs751638154	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67843786	TTTTTTTTTTTTGAG[A/G]TGGAGTTTTGCTCTT	2186
rs751656929	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67839657	TTGCTGAGTAGCAGT[C/T]CCTTATATGAGTGTA	2186
rs751662329	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67922175	CTGCAGTCCCCTAAA[A/G]TCACTTCTCTTTGGC	2186
rs751673345	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67832253	AGCATGTTTCTTAAT[-/T]TTAAAAAAAAAAAAC	2186
rs751687516	snp	A/T	0.000561621	0.016748	intron-variant	BPTF	GRCh38.p7	17:67929333	GCTTCATCTTTTTTT[A/T]AGGCGTTGTTCAAGT	2186
rs751731898	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67871017	ACCTCGTGATCCGCC[C/T]GCCTCGGCCTCCCAA	2186
rs751822693	snp	C/T	1.79438e-05	0.00299526	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67826171	GGAGGAGGAGGAGGA[C/T]GGCGACGCCGAGGAG	2186
rs751823736	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67862241	TCGGACTCCGAAAGT[A/G]CTGGGATTACAGGCG	2186
rs751837615	snp	G/T	3.30885e-05	0.00406733	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912874	ACGACAGTGACAGAC[G/T]CCCTGACCACCACGG	2186
rs751841332	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67826929	TAGTAGGGGAACCTT[A/G]TCTGGTCCTGTGTGT	2186
rs751852324	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67849019	TTTGGTTAAGCTTCA[A/G]CTTCCCTTTGCATCA	2186
rs751873384	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67908268	GGTTGAAGCAATTCT[C/T]CTGCTTCAGTCTCCC	2186
rs751874178	in-del	-/TAT			intron-variant	BPTF	GRCh38.p7	17:67872805	AAGTGTTCTTTAAAA[-/TAT]AGGAATTAAGGGCTG	2186
rs751882552	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67910296	TTTCCTCTTTTGGCT[A/G]TACGAATAATGCTGC	2186
rs751890899	snp	A/T			upstream-variant-2KB	BPTF	GRCh38.p7	17:67824460	ATTACTTTTCGGTTG[A/T]CACTTCTCTCAATAA	2186
rs751904000	snp	C/T	1.71971e-05	0.00293227	intron-variant	BPTF	GRCh38.p7	17:67874804	ATTTTTTTGTTTGTT[C/T]TACACATTATAGAAG	2186
rs751928934	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67883542	ATGTCTTTCTTTTCT[A/G]AGTAGCCATTTTTAT	2186
rs751956168	in-del	-/G	2.2758e-05	0.0033732	intron-variant	BPTF	GRCh38.p7	17:67875777	CAATGCCTCTGTAAT[-/G]GGGGGGAATCCTTCC	2186
rs751958852	snp	G/T	1.656e-05	0.00287745	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67826235	ATGGAAGAGGACGAC[G/T]ATGACTCCGATTATC	2186
rs751967188	snp	A/G			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67896987	TAAGTCTCTGATAAG[A/G]TTATCAAGGGGGAGG	2186
rs751976321	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67964865	TTAGCTGGGCGTGGT[A/G]GCGGGCGCCTGTAGT	2186
rs752013306	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67885896	CGAGTCAGTGAGTTA[A/G]AGTTGGGTCCTCACC	2186
rs752021524	snp	C/T	3.2956e-05	0.00405918	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67922930	CTGGCCCTGTTATTA[C/T]TGAAACCTGGGTAGC	2186
rs752025954	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67913500	TCTGATTTTCTGAGT[C/T]ACTGCTCTGGGAACA	2186
rs752027687	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67834740	TTAATTACAACCTAC[G/T]TTGGGCAGGGACAGT	2186
rs752029145	snp	C/T	0.000115393	0.00759493	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67911625	TGACACCATTGTTTC[C/T]TCTTCCAAGAGTGCT	2186
rs752029328	snp	C/G	2.01404e-05	0.00317329	intron-variant	BPTF	GRCh38.p7	17:67909534	TGACATATTAAAGTG[C/G]TAATACTCTGGAAAT	2186
rs752070910	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67835855	TAATTTTAGTAGAGA[C/T]GGGGTTTCACCATGG	2186
rs752075111	snp	C/T	1.65386e-05	0.00287559	intron-variant	BPTF	GRCh38.p7	17:67903970	CATTTCTGAGACTTT[C/T]ATTCTGAAACTTTGA	2186
rs752080041	snp	G/T	1.64811e-05	0.00287059	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67911733	ACTGGGATGTGACTC[G/T]GAATCTAATAGCACT	2186
rs752082182	in-del	-/C			intron-variant	BPTF	GRCh38.p7	17:67890336	CCGTTTCATATTTTT[-/C]CTGTTTATTTCTTCT	2186
rs752134734	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67901743	TTTAGAAGTTCAATA[C/T]TAACTCAGCATGAGT	2186
rs752138287	snp	A/C	1.65446e-05	0.00287612	missense, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67886142	GAAGAACCTAACAAG[A/C]CATGTGAGAGCAGTA	2186
rs752157841	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67884472	CCAGGCTAGAGTGCA[A/G]TGGCGCAATCACGGC	2186
rs752190494	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67830949	TCAAATCACAGAGAT[A/G]CTGTTGAACCACTGG	2186
rs752201975	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67881652	AGGACTATAGACGCG[C/T]GCCACCACATCTGGC	2186
rs752205440	snp	A/G	1.66087e-05	0.00288168	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911297	CTGAGGACTTGATTC[A/G]GGGATGTTCAGAAAG	2186
rs752225451	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67839199	TGTTAAATGTTAGTT[A/G]TAACGATAGGCATCT	2186
rs752260529	snp	C/T	3.84971e-05	0.00438715	intron-variant	BPTF	GRCh38.p7	17:67893773	AATATACTAAATGTT[C/T]ATAAAATGATTGTTG	2186
rs752313368	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67836851	AGTGCTGTGCAAAGA[C/G]TAAAATGTTTTAAGG	2186
rs752360560	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67915360	AAGGGACTTGGTAAC[C/T]ACTGCAGCAAGGAGC	2186
rs752361872	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67907358	ATCAAAGTTTATCAC[-/T]TTTTTTTTTTTTTTT	2186
rs752363188	snp	A/G	1.65529e-05	0.00287683	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911413	ATTCGGAGCCCAGAA[A/G]CAAAATGTCCGAAAC	2186
rs752365883	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67904489	ACATTTTACATGCTA[A/T]AAAGGAGTATTAGTT	2186
rs752388274	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67868386	GTATTCTCAGGGATT[A/G]CTTCCAGAGCCCTCT	2186
rs752393446	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67917873	CTGGAATGCAGTGGC[C/T]GGATCTTGGCTCACT	2186
rs752396891	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67978500	GACGGGGTTTCACCA[C/T]GTTGACCAAGCCGGT	2186
rs752406634	snp	G/T	0.000191406	0.00978092	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	BPTF	GRCh38.p7	17:67825537	AGAAACAAGATGGCG[G/T]CTGAAGGCGATCCGG	2186
rs752412298	snp	A/G	1.64749e-05	0.00287005	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67918732	TAGACTTCAGACAGT[A/G]AAGTCCTTAGCTGGA	2186
rs752419938	in-del	-/A			intron-variant	BPTF	GRCh38.p7	17:67829642	ATGTGTAGATAGAAG[-/A]AAAAAAGTTTTAGAA	2186
rs752421122	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67855678	GCAGGGTTATAGTGT[A/G]GACTGAGTATCTGAC	2186
rs752423646	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67832300	TGCACTTTAAAAGAT[C/T]GAAGGTGACCGTATA	2186
rs752432822	in-del	-/AA			intron-variant	BPTF	GRCh38.p7	17:67864528	GTGAGACTCCATCAC[-/AA]AAAAAAAAAAAAAAA	2186
rs752448589	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67902410	CGCCTTACTCCTGTA[C/G]CCTGAGACTGTCAGG	2186
rs752484829	snp	A/G	1.71129e-05	0.00292509	missense, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67875571	AGCCAACAGAAGTTG[A/G]GGATAAAGGTAACTC	2186
rs752505038	snp	A/G			intron-variant, utr-variant-5-prime	BPTF	GRCh38.p7	17:67889146	CTGTAGCCTGCTGCC[A/G]GGCTGCATCACAAGG	2186
rs752551454	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67938257	TTATGATGGCAATGT[A/G]TCTGTACCAGGTGAT	2186
rs752552070	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67980463	TCATTATAAGCCCCT[C/G]TATGCTTTTTCATTT	2186
rs752556972	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67841011	AGAGCATAAGTTTTA[A/C]ATTTTGATAAAGTCT	2186
rs752572545	in-del	-/TTTG	1.77694e-05	0.00298067	intron-variant	BPTF	GRCh38.p7	17:67874794	TATAGGAATAATTTT[-/TTTG]TTTGTTTTACACATT	2186
rs752642540	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67939005	ACTTTACTGGTGATA[C/T]CAAGGTTTGGCAGGG	2186
rs752647108	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67827004	TGTTAAATGGCTGAT[G/T]AAAAAGCAACGCAGA	2186
rs752659240	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67863731	CTATTTCCAAATAAG[A/G]TCACATCCTGAGGTT	2186
rs752664024	snp	G/T	5.20134e-05	0.00509941	intron-variant	BPTF	GRCh38.p7	17:67909796	GAGGGCAGCCTGGGG[G/T]TGATAAGAATGCACT	2186
rs752664029	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67856413	CTCTCCTCTGTGCAT[A/G]GTCTGTTTCTTCTAA	2186
rs752678842	snp	C/G	1.64808e-05	0.00287057	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67853993	ATATTGGAAGAAAAA[C/G]ACATCCCGCCCCTTG	2186
rs752678946	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67877643	TTTTTTTTTGAGAGA[A/G]AGTCTCACTCTTTCA	2186
rs752700468	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67839826	GGAGTATGATTTCTG[C/G]GTTGTATGTTTATGA	2186
rs752703236	snp	C/G	1.64844e-05	0.00287087	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67893537	GAATAAGCACCAGCA[C/G]AGAGAAGACCATGAT	2186
rs752708632	snp	C/T	1.64993e-05	0.00287218	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912197	GTGGTAATGTTGAAC[C/T]AAAGGTTAATAATAT	2186
rs752719289	snp	C/T	1.67956e-05	0.00289784	intron-variant	BPTF	GRCh38.p7	17:67866706	AGAGGGGCATTTTCT[C/T]ATTTTATTTTTGTTA	2186
rs752720319	in-del	-/G			intron-variant	BPTF	GRCh38.p7	17:67906061	ATTTAAAAAAATAAT[-/G]GAGGTTTTTTTTGGG	2186
rs752730345	snp	C/G			intron-variant, utr-variant-5-prime	BPTF	GRCh38.p7	17:67889940	TGCTCAGTACCCTCT[C/G]TCCATTTTGACTTAT	2186
rs752734444	snp	A/G	3.29457e-05	0.00405854	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67854156	CAGCTCTGGTGAGCC[A/G]AGAGCAGTGCACACT	2186
rs752742322	in-del	-/TA			intron-variant	BPTF	GRCh38.p7	17:67880949	GGTGTATGTATATTA[-/TA]TATATATATACACAC	2186
rs752743895	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67910537	GGGCGTGGTGGCTCA[A/T]GCCTGTAATCTCAGC	2186
rs752783752	snp	A/G	1.6676e-05	0.00288751	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67929467	ACCTCAGGCTCTGGA[A/G]GAACCACAAGCAATT	2186
rs752790565	in-del	-/CT			intron-variant	BPTF	GRCh38.p7	17:67871097	ATTTCTAATGTATAA[-/CT]CTCTGGTTTTTATCT	2186
rs752804882	in-del	-/A	0.00018986	0.00974135	intron-variant	BPTF	GRCh38.p7	17:67931883	TTTTTAAAGCATTTT[-/A]ATTCATTGTTCTTTG	2186
rs752836930	snp	A/T	1.66515e-05	0.00288539	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67913115	AGGTCCCTTATTTTA[A/T]TTACAATGCAAAACC	2186
rs752886514	snp	A/C	1.65384e-05	0.00287557	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912886	GACTCCCTGACCACC[A/C]CGGGAGGCACACTGG	2186
rs752892356	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67849110	ACCCTTTCTGCTTGG[C/T]AAGGGGAGTATCCAT	2186
rs752915826	snp	C/T	5.05276e-05	0.00502606	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67874823	ACATTATAGAAGAAA[C/T]TTTGGAATCCATAAG	2186
rs752929550	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67973783	AACTGCTAGGATTAC[A/G]GACGTGAGCCACCCC	2186
rs752941718	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67850512	TAGCTGGGAGTACAG[G/T]TGTGTGCCACCATGC	2186
rs752942943	snp	C/T	1.64825e-05	0.00287071	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67911637	TTCTTCTTCCAAGAG[C/T]GCTTTACATTCATCA	2186
rs752959594	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67886071	ATTGTCTTTTCTGAC[A/T]ATTCGTCATTTTTCA	2186
rs752976722	snp	C/T			synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67911445	AAATTCCATTGAAAA[C/T]GACATAGAAGAAAAA	2186
rs752996633	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67865525	CTTGTCCATGTCCAC[A/G]TATCTTACAAGCAAA	2186
rs752998112	snp	A/C	1.64806e-05	0.00287054	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911762	CTTTGGAAAATAGTT[A/C]TGATACCGTGTCTAT	2186
rs753026918	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67917572	CAGAATGTTTTTGTC[C/T]GTTTGGAAAGGTCTT	2186
rs753044214	in-del	-/A	0.00585565	0.0537916	frameshift-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67903834	GAAAAGGAGAAAGTC[-/A]AAAAAAAAAGAGAAG	2186
rs753052865	snp	C/T	2.00688e-05	0.00316765	intron-variant	BPTF	GRCh38.p7	17:67909540	ATTAAAGTGCTAATA[C/T]TCTGGAAATAACGTA	2186
rs753068387	snp	C/G	1.71135e-05	0.00292514	intron-variant	BPTF	GRCh38.p7	17:67826349	CCAGGTACCCACCCA[C/G]CCCAGTTGCTGCAGA	2186
rs753081936	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67934084	ATTCATAGGCTTTTT[A/G]GTGGAAAAGTAGTTC	2186
rs753082857	in-del	CCGGTT/TGTC			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67896468	TGAGTAACTAGAAAC[CCGGTT/TGTC]CCCCCAGTGCACATA	2186
rs753113358	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67884664	CAAGTGATCTGCCTG[C/T]CTCAACCTCCCAAAT	2186
rs753134267	in-del	-/A	1.67584e-05	0.00289464	frameshift-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67912194	TAAGTGGTAATGTTG[-/A]ACCAAAGGTTAATAA	2186
rs753150548	snp	C/T	1.65132e-05	0.00287339	intron-variant	BPTF	GRCh38.p7	17:67924636	AGGCCCAAATGGAGG[C/T]TCTTTCAAAACAAAA	2186
rs753188280	snp	A/G	8.8262e-05	0.00664253	intron-variant	BPTF	GRCh38.p7	17:67891835	CTTTGTGGCCTATTC[A/G]TTTGACAGTAGGTGA	2186
rs753201980	in-del	-/TCTTC			intron-variant	BPTF	GRCh38.p7	17:67960136	TCCTTTGCTTTCTCT[-/TCTTC]TCTTCCCTCTGAATT	2186
rs753204042	snp	A/T	3.31598e-05	0.00407171	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912476	ATTCAGTTAATCAGG[A/T]AGAAGATATGGAAAT	2186
rs753210939	snp	A/G			missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67904826	ATGTGAATTACAGAA[A/G]GTCGTTAGAAGGAAG	2186
rs753227133	snp	A/G	1.64762e-05	0.00287016	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67894139	TGTGATGCTACCAAT[A/G]TGGCGAGAATCTTTA	2186
rs753236097	snp	A/G	1.65078e-05	0.00287291	synonymous-codon, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67886282	AAATGGAGAAAGAGA[A/G]TCTCATACACCTGTC	2186
rs753237497	snp	C/G	0.00019974	0.00999151	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	BPTF	GRCh38.p7	17:67825561	GATCCGGAGTGGGGC[C/G]CCAGCAATTCGGATT	2186
rs753249174	snp	C/T	3.37524e-05	0.00410793	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67909633	ATAAAAGAAAATGTT[C/T]ACGAAGTCCAAAAAA	2186
rs753269856	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67885480	CTGTAGTCCCAGCTA[C/T]TCAGGAGGCTGAGGC	2186
rs753283675	snp	A/G	0.000297698	0.0121967	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911539	TTCATCGATGACTCT[A/G]AACTAGCCAGTGCAG	2186
rs753288973	snp	A/G	3.29484e-05	0.00405871	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67854639	TCTGTGTAGCACACA[A/G]GGTGCCTGGTGTGAC	2186
rs753307941	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67930301	CCTCCTGGGTTCAAG[C/T]GATTCTCCTGCCTCA	2186
rs753320986	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67932209	TGACAGTAAAATAGG[C/T]TGAAGTATGCTTATT	2186
rs753371905	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67915408	CCTGTAGATCACATT[A/C]ATGGAAAGTACTTCC	2186
rs753373945	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67916404	AGACCAGCCTGGCCA[A/C]AGTGGTGAAACCCCG	2186
rs753376936	in-del	-/A	3.34275e-05	0.00408811	splice-donor-variant	BPTF	GRCh38.p7	17:67875022	GGAAAATCTGAGGGT[-/A]AAAAAAATTACTTGA	2186
rs753426427	in-del	-/AT			intron-variant	BPTF	GRCh38.p7	17:67827442	AAGGCTGCTTTGTAC[-/AT]AGTCACAATTTACTA	2186
rs753427019	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67917276	TAGCTGGGATTACAG[C/G]CGCCCGCCACCATAC	2186
rs753445917	in-del	-/TTTTTTTTTTTTT			intron-variant	BPTF	GRCh38.p7	17:67925995	ACCTAACATATTACT[-/TTTTTTTTTTTTT]TTTTTTTTTTTTTTT	2186
rs753482140	snp	A/C	1.74269e-05	0.00295181	intron-variant	BPTF	GRCh38.p7	17:67903780	GTCTTTCTATGCATG[A/C]ATTCTTAGGTTACAC	2186
rs753489951	snp	A/G	3.35689e-05	0.00409674	intron-variant	BPTF	GRCh38.p7	17:67919971	CTTTTTAGTCTCTGA[A/G]TATTTCAGTTGGTTA	2186
rs753530186	snp	C/G	1.67144e-05	0.00289084	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912061	AAGAATAATGAAAAT[C/G]GAGAGTCTGAAAAGA	2186
rs753570009	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67855746	GTGTCTTCAGCTTCT[A/G]AAGTCTTCAAAGCCC	2186
rs753570371	snp	C/T	3.33056e-05	0.00408065	missense, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67875684	TGTCTCTCAGAAACC[C/T]CCGATAGCAGCAACA	2186
rs753625640	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67891365	CTACACAGATAATTA[C/T]CTAAATTCCCTAGTG	2186
rs753634471	snp	A/G	3.36746e-05	0.00410319	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912220	AATAATATAAATAAA[A/G]TAATCCCTGAGAATG	2186
rs753641102	snp	G/T	1.64727e-05	0.00286986	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67854184	ACTCATGGCAGAGAT[G/T]CATGTTGTGCTTTTG	2186
rs753654535	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67939094	CTTCAACTTAGTACT[A/G]TATTCCTACTATGAA	2186
rs753677359	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67904311	CTGGAATTACAGGCA[C/T]GAGCCACTGCTCCTG	2186
rs753684485	snp	C/T	1.65119e-05	0.00287327	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67910963	ATGAAAACAGAGTCA[C/T]ATGTAAATTGTCAGG	2186
rs753687500	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67924385	CTCCCACAGTGCTGG[C/G]ATTACAGGCATGAGC	2186
rs753711346	snp	C/T	1.64735e-05	0.00286993	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67854325	GGTGCTGCGGGTGTA[C/T]TGTGAGAGTGATAAG	2186
rs753745397	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67829511	GAGTTCTAAACTTTT[A/G]GAACATGCCCACTTG	2186
rs753803653	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67850799	TGGACATTTTGGTTG[C/T]TTTCAGCTTGGTTGA	2186
rs753822482	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67865637	AGGCTCACTCTCATC[A/G]AGTGCCTCACACATA	2186
rs753831908	snp	A/G	3.31923e-05	0.0040737	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911122	GAAAAACAGCGACTC[A/G]AAAAAATCAAGTTGG	2186
rs753832966	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67849980	AGACTCTATTCTAGG[C/T]CTATTGAATCAGTGA	2186
rs753878185	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67899067	ACAATTTTGTTCCAC[G/T]CTGAACTCCACCAAA	2186
rs753910410	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67866914	TATACGGCATAGCCT[C/G]TTGCTGCTAGGCTGC	2186
rs753975034	snp	G/T	3.31939e-05	0.0040738	intron-variant	BPTF	GRCh38.p7	17:67918664	TATGAATGTGTATGT[G/T]TATGTATATACATAT	2186
rs754041893	snp	A/T	1.67528e-05	0.00289415	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67909652	AAGTCCAAAAAAAAT[A/T]AAAATAGAGCCTGAT	2186
rs754051052	snp	G/T	6.97423e-05	0.00590477	intron-variant	BPTF	GRCh38.p7	17:67826360	CCCAGCCCAGTTGCT[G/T]CAGACTCCTTCCCCA	2186
rs754055733	snp	C/T	3.96456e-05	0.0044521	intron-variant	BPTF	GRCh38.p7	17:67909552	ATACTCTGGAAATAA[C/T]GTAAATTATCGTTAC	2186
rs754108327	snp	C/G	1.67595e-05	0.00289473	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67853951	ACAGGTAGGCGAAAA[C/G]CAAGAGTACATCGGC	2186
rs754110246	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67886330	AGGTAAGAATATACT[C/T]CATCCATTCCTTTAA	2186
rs754112249	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67900434	ATATTCAAGGCCTGT[A/G]TAAAGCAATCTTTAG	2186
rs754185232	snp	A/G	1.69318e-05	0.00290957	synonymous-codon, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67891860	AGGTGATTTCAAATC[A/G]GAGAAGTCCAACGGG	2186
rs754206695	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67841638	AATTCCTGGGCTCAA[A/G]CAGTCCACCCACCTC	2186
rs754243655	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67970159	AATTGCTTGAACCTG[C/G]GAGGTGGAGGTTGCG	2186
rs754265808	in-del	-/A			intron-variant	BPTF	GRCh38.p7	17:67868157	GTTACTCAACTCTTT[-/A]TTTTTTTAAGTTATA	2186
rs754270291	in-del	-/T	1.82261e-05	0.00301872	intron-variant	BPTF	GRCh38.p7	17:67913206	GTACTTTAAAATGTA[-/T]TTTGGGGGAGGGAGA	2186
rs754320726	snp	A/G	1.66626e-05	0.00288635	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912622	GTCAATGGAGAATCT[A/G]AAAGAAAAACCGTCA	2186
rs754336182	in-del	-/TA			intron-variant	BPTF	GRCh38.p7	17:67843227	ATGTAGATATATACC[-/TA]TATATCTACATACAT	2186
rs754369900	snp	A/G	3.314e-05	0.00407049	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67911424	AGAAACAAAATGTCC[A/G]AAACAAAATTCCATT	2186
rs754379845	snp	A/G	2.30556e-05	0.00339518	intron-variant	BPTF	GRCh38.p7	17:67854802	TTGTATGCATTTAAA[A/G]TTAGACTAGTTTCCT	2186
rs754385647	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67845023	GCTGGGATTACAGGC[A/G]TGAGCCACTGCGCCC	2186
rs754389929	in-del	-/TTTT			intron-variant	BPTF	GRCh38.p7	17:67919747	GCTTCTGTCCTAGGC[-/TTTT]TATTATTTTGATTGA	2186
rs754401657	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67830006	AATTGAAATCACCTA[A/G]TTTTGCTTAAGCTAA	2186
rs754484719	snp	G/T	3.31049e-05	0.00406834	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912381	AGGTAACTACCGAGA[G/T]AGCCTTGAGACCCTG	2186
rs754487669	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67893053	AACTTGAAAAAAATG[A/G]TAGGTGAGTAATTTA	2186
rs754522302	snp	A/G	1.66333e-05	0.00288381	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911284	AATAATGATCAACCT[A/G]AGGACTTGATTCAGG	2186
rs754539493	snp	C/T	3.33444e-05	0.00408303	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911165	AGGGTATAGGAAAGA[C/T]TTCTACAAATTCTTC	2186
rs754542236	snp	C/T	1.64738e-05	0.00286995	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67854625	GTGGCAGTGTGAAGT[C/T]TGTGTAGCACACAAG	2186
rs754543522	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67835780	ACGCCATTCTCTTGC[C/T]TCAGCCTCCCAAGTA	2186
rs754549101	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67860324	TATGTGGACTCCTCA[C/T]GATAGTTTTAAAGCC	2186
rs754562454	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67867148	TTCATTTTCCCAAGA[C/G]AACCTTGTTCATTCC	2186
rs754562461	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67881336	ATACTTTATAAAGAA[C/T]GTGCTGGTTAATTGA	2186
rs754599655	snp	A/T			missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912015	TAATAAATGTAGTGA[A/T]CAAATAAAGCTAAAA	2186
rs754695790	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67853902	GTAGAAATGATGTAA[C/T]GTATTGATTTGTAAT	2186
rs754707999	snp	C/T	1.69335e-05	0.00290972	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67913150	TTGGATATATGGCCA[C/T]ATCCTTCTCCTAGAC	2186
rs754777936	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67915223	CCATTCCCTTATGCC[C/T]ATCCTCCCAGGCCCT	2186
rs754782595	snp	A/G	6.59152e-05	0.00574049	missense	BPTF	GRCh38.p7	17:67931947	CGCCCTGGTATGACC[A/G]TGATTAGAACACCAC	2186
rs754801816	snp	A/G	1.64806e-05	0.00287054	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911783	CCGTGTCTATTCAGG[A/G]TAGCAGTGAAGAAGA	2186
rs754808675	snp	A/G	3.70165e-05	0.00430196	intron-variant	BPTF	GRCh38.p7	17:67893761	TTTATTGCTGTAAAT[A/G]TACTAAATGTTTATA	2186
rs754812950	snp	C/T			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67887983	ATATTGTTTCTAACC[C/T]TATGGCCAGGGCAGG	2186
rs754821714	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67852617	TTCTGTAGATGCATC[A/G]TAATTCATTTGACTA	2186
rs754836697	in-del	-/CA			intron-variant	BPTF	GRCh38.p7	17:67900789	TTGAGGAGGGAGGAT[-/CA]CCTGAAGTGAGAAGT	2186
rs754868273	snp	A/G	1.65433e-05	0.002876	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67874978	GAAAAAGACAGTGAC[A/G]ACAAAACACCAGATG	2186
rs754887842	snp	A/G	1.6522e-05	0.00287414	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67853970	GAGTACATCGGCCTC[A/G]TTCTCCTATATTGGA	2186
rs754903159	snp	C/T	1.90315e-05	0.0030847	intron-variant	BPTF	GRCh38.p7	17:67826388	CCACCTCCTCTGCCC[C/T]CCCCCCTTGCTCACT	2186
rs754907231	snp	A/G			intron-variant, utr-variant-5-prime	BPTF	GRCh38.p7	17:67889078	TGAAGAGTTTGTGTA[A/G]GCTTCTGCCTGCTGG	2186
rs754938218	in-del	-/TTACA			intron-variant	BPTF	GRCh38.p7	17:67952727	ACGAAAGTCCATAGT[-/TTACA]TTAAGGTTCACTCCT	2186
rs754941855	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67920736	GCTAAGAGAGTAATA[C/T]TGGAAAAGAAGATTA	2186
rs754983178	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67966339	ATTTTGTGACTTCTA[A/G]GCTTGTGCTCCATTC	2186
rs754993267	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67877568	ATGATTAAAACTTAT[C/T]GACAAAAGATAACTG	2186
rs754993447	snp	C/G	1.71446e-05	0.0029278	intron-variant	BPTF	GRCh38.p7	17:67928614	CAGGTATGGAACTAT[C/G]ATTAAGTAAAAGATT	2186
rs755046181	snp	C/T	1.85606e-05	0.0030463	intron-variant	BPTF	GRCh38.p7	17:67892045	AAGAGGTGTGTTCTT[C/T]CTGTTTAAAACAAAA	2186
rs755054106	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67891713	TACTTGCTTTGCCAT[G/T]CAAGGGCCTTTTTTT	2186
rs755055269	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67826951	CCTGTGTGTTTGTTT[C/T]TATTCTTCGAGTGCT	2186
rs755059684	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67862311	AATATTATACACTTC[A/G]TAAGGTGAGGAAAAT	2186
rs755063081	snp	C/T	0.00011536	0.00759387	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67866609	ATGCGTGAAGAAATC[C/T]ACCGACACATGGACA	2186
rs755088532	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67839679	ATGAGTGTATCACAG[C/T]GCATTTATCCATTCA	2186
rs755088972	snp	G/T	1.66407e-05	0.00288446	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	BPTF	GRCh38.p7	17:67893405	AGGAGAAATTTCACG[G/T]TTGAGCACCAAAAAG	2186
rs755105824	snp	C/T			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67897011	GGGGAGGAAATAATA[C/T]AGCACAAATAACCAA	2186
rs755112422	snp	C/T			upstream-variant-2KB	BPTF	GRCh38.p7	17:67823893	GGCTCACTGCAACCT[C/T]CACCTCCCAGGCTCA	2186
rs755120998	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67876147	CGTGTAATATTTATA[A/G]CATTTCAAACCGTAG	2186
rs755144865	snp	C/T	6.65668e-05	0.00576879	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67912753	AAATTGTGCAAAATC[C/T]ACTGTCACAACCACC	2186
rs755162613	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67868193	ATATATATCTCAAAA[C/G]TTTAAATAGTATAAA	2186
rs755192817	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67840229	CACCTCTCAGCTTCC[C/G]CAGTAGCTGGGATTT	2186
rs755195316	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67908299	AAGTAGCTGGGACTA[C/T]AGGCTCGTACCACCA	2186
rs755195965	snp	C/G	3.30382e-05	0.00406423	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911557	CTAGCCAGTGCAGAT[C/G]ATATTGGTACTTTGA	2186
rs755196353	snp	C/G	1.65444e-05	0.00287609	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67912876	GACAGTGACAGACTC[C/G]CTGACCACCACGGGA	2186
rs755241808	snp	A/G	1.77197e-05	0.00297649	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67826173	AGGAGGAGGAGGACG[A/G]CGACGCCGAGGAGAC	2186
rs755295349	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67834854	AAGAAAGCCTGTGGA[A/T]TCTTTTCACGCTCTA	2186
rs755307107	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67932788	AAATCAAATTACTAC[A/G]AAAGCTACAAAAGAT	2186
rs755353126	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67919860	TGTTGCAGTCTAGCA[-/T]GTGATCCTGCTAGAT	2186
rs755369393	snp	C/G	1.65493e-05	0.00287652	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67826242	AGGACGACGATGACT[C/G]CGATTATCCGGAGGA	2186
rs755377961	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67871648	GATGGCTTCTAAAAC[C/T]TGGTAGGTTAATTCT	2186
rs755390071	snp	A/G	1.65367e-05	0.00287543	synonymous-codon, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67886144	AGAACCTAACAAGAC[A/G]TGTGAGAGCAGTAAC	2186
rs755392259	snp	A/T	1.64852e-05	0.00287094	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911626	GACACCATTGTTTCT[A/T]CTTCCAAGAGTGCTT	2186
rs755409311	snp	A/G			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67897503	AGGGGTCCACCTAGA[A/G]AGAGTGGACCAAGAT	2186
rs755442563	in-del	-/TTC	1.65217e-05	0.00287412	intron-variant	BPTF	GRCh38.p7	17:67894018	AATAATTTCTCTCAT[-/TTC]TTCTGAAATACAGGG	2186
rs755479952	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67917463	ACTATTCATTGTAGA[A/C]TTTGAAAACTACACT	2186
rs755481528	snp	A/G	3.29451e-05	0.00405851	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67854371	CTTCCTTACCAAGAG[A/G]CAGAGGACTACCCAT	2186
rs755482689	in-del	-/C			intron-variant	BPTF	GRCh38.p7	17:67930827	GCATGTGCCTGTAGT[-/C]CCAGCTATTCCCAGC	2186
rs755514479	snp	G/T	1.64868e-05	0.00287109	missense, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67886261	TAAGGCAGCTGATGA[G/T]CCTGAAAATGGAGAA	2186
rs755528675	in-del	-/CATC	0.000415258	0.0144034	intron-variant	BPTF	GRCh38.p7	17:67886331	GGTAAGAATATACTT[-/CATC]CATTCCTTTAAAGGG	2186
rs755540105	snp	A/G	1.64784e-05	0.00287035	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67922932	GGCCCTGTTATTATT[A/G]AAACCTGGGTAGCAG	2186
rs755578868	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67919861	TGTTGCAGTCTAGCA[G/T]TGATCCTGCTAGATG	2186
rs755592862	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67846295	AGCAGTTTTAGAGCA[G/T]CCTGGGCAGCATAGA	2186
rs755627189	snp	C/T	1.6554e-05	0.00287693	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911414	TTCGGAGCCCAGAAA[C/T]AAAATGTCCGAAACA	2186
rs755639145	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67913665	CATGATAAACATTTG[C/T]TTTGGAGTTCTCTGT	2186
rs755644633	snp	A/T	1.65784e-05	0.00287905	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911315	GATGTTCAGAAAGTG[A/T]TTCCTCAGTTCTTAG	2186
rs755649926	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67832333	AATAATTAAAATGCA[C/T]GTAAATATAATTATA	2186
rs755680201	snp	A/G	1.6476e-05	0.00287014	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67894137	GTTGTGATGCTACCA[A/G]TATGGCGAGAATCTT	2186
rs755693099	snp	C/G	1.64787e-05	0.00287038	missense	BPTF	GRCh38.p7	17:67931965	ATTAGAACACCACTC[C/G]AACAGTCAACACTAG	2186
rs755698091	snp	A/G	8.28507e-05	0.00643572	intron-variant	BPTF	GRCh38.p7	17:67893993	TTTTAATTTAAGGTC[A/G]ACCTAGTGAAATAAT	2186
rs755701288	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67830960	AGATGCTGTTGAACC[A/G]CTGGTGTAGCTGTTT	2186
rs755737035	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67930043	ATGGCTTGAGCCTGG[C/G]AGGGGAAGGTTGCAG	2186
rs755743169	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67902517	GTACATTAGCTCCCA[C/G]TGAGGATCTGCTCCC	2186
rs755780851	snp	C/G	1.65715e-05	0.00287845	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67874993	GACAAAACACCAGAT[C/G]ATGACCCTGAGCAAG	2186
rs755794388	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67926451	TGCCTCAGCCTCCCG[A/G]GTAACTGTGACTATA	2186
rs755796619	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67938261	GATGGCAATGTATCT[A/G]TACCAGGTGATCTCT	2186
rs755816364	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67937057	CCCTCATGAAACTTA[C/T]AGTCTAGTGGAAAAG	2186
rs755834083	snp	A/G	8.50246e-05	0.00651959	missense, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67875576	ACAGAAGTTGGGGAT[A/G]AAGGTAACTCTGTGT	2186
rs755854840	in-del	-/GAG/GAGGAG/GAGGAGGAG	0.0380509	0.132664	cds-indel, nc-transcript-variant	BPTF	GRCh38.p7	17:67826150	GAGGACATGGTCTCC[-/GAG/GAGGAG/GAGGAGGAG]GAGGAGGAGGAGGAG	2186
rs755893548	snp	A/C	1.65666e-05	0.00287802	intron-variant	BPTF	GRCh38.p7	17:67932057	CATTTTACATCTCAA[A/C]AGCCAGTCTAGGAAA	2186
rs755903541	snp	A/G	1.66866e-05	0.00288842	intron-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67918871	TATTTTCTAATTTAA[A/G]TTTAAAAGCTAAAAT	2186
rs755913402	in-del	-/G			intron-variant	BPTF	GRCh38.p7	17:67974534	ATTACCCCCTCTTCA[-/G]ATGCCGGTCGCCAGC	2186
rs755926801	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67855706	GACATCCTGTAGATA[C/T]ATGGTCAGAGGGATG	2186
rs755942082	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67950009	CAGTGAGCCAAGATC[A/G]CACCACTGCACTCCA	2186
rs755963308	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67876259	CATTTTCAGTTTTTA[A/C]AATTAAAGTTATACT	2186
rs755973532	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67871396	CAGTGAGCCGAGATC[A/G]TGCCACTGCCCTCCA	2186
rs756018267	snp	A/G			intron-variant, utr-variant-5-prime	BPTF	GRCh38.p7	17:67889156	CTGCCAGGCTGCATC[A/G]CAAGGATCCACTGCT	2186
rs756066816	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67975451	GCATGTAAAAATGCA[G/T]TATACTTAGATATGC	2186
rs756067150	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67827090	GTTAAATCAAAAATA[A/G]AAGTACAAAACTACA	2186
rs756087026	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67846293	CCAGCAGTTTTAGAG[A/C]AGCCTGGGCAGCATA	2186
rs756104537	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67841033	ATAAAGTCTAATTTA[C/G]CACTTTTTTTCTTTT	2186
rs756115840	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67924180	GAGATGGGTCGAACT[C/T]CTGATCTCAAGCAAT	2186
rs756116638	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67865610	GTTTGCCATTGAGTA[A/G]ACAGGAAAATCAGGC	2186
rs756145960	in-del	-/A			intron-variant	BPTF	GRCh38.p7	17:67833259	CTTTTTTTTTTTTTT[-/A]ATGGAGACAGGGTCT	2186
rs756187584	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67849286	TTTGCTGCACCTCCA[C/T]TTCAGGGCAGCTTTT	2186
rs756212446	in-del	-/TAAGCTTTGTTT			intron-variant	BPTF	GRCh38.p7	17:67866370	TTGAGTTTTAGTGCA[-/TAAGCTTTGTTT]TAAGTTTTCACTGGG	2186
rs756236945	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67884770	TTAAATACTCCAATG[A/G]ATAGCTAGCTCTATA	2186
rs756237649	snp	C/T			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67897116	GCAGTCACCTGAGGT[C/T]GGGAATTCGAGACCA	2186
rs756238754	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67863978	TGCCAGTCTGTCTTC[C/T]CTTTGCCACCCTATG	2186
rs756247991	snp	G/T	1.6759e-05	0.00289469	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67874831	GAAGAAATTTTGGAA[G/T]CCATAAGAGCCAAAA	2186
rs756272309	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67898764	GGAACAAAAAAGATA[C/T]CCACTATTGGCCAGG	2186
rs756283171	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67849754	ACCAGCCTGGCCAAC[A/G]TGGGGAAACCCCTTC	2186
rs756283238	snp	A/G	1.64808e-05	0.00287057	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67911649	GAGTGCTTTACATTC[A/G]TCAGTGCCTAAAAGT	2186
rs756300830	snp	A/T	1.6546e-05	0.00287624	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67826257	CCGATTATCCGGAGG[A/T]GATGGAAGACGACGA	2186
rs756303244	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67886360	AAGGGAAGTTTTTTC[-/T]TTTTTTTCTTTTTTT	2186
rs756303561	in-del	-/TGGA			intron-variant	BPTF	GRCh38.p7	17:67873996	TAAGAAAATGCTGGA[-/TGGA]TGGATGGATGGATGG	2186
rs756305657	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67858204	TTAAATGTATATTCT[A/G]TGTCTTTTGGTTTGG	2186
rs756336187	snp	C/T	1.6486e-05	0.00287102	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67904773	GATTAGTAAAACTCA[C/T]GTTTATAGGTTTGTT	2186
rs756382735	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67835126	GAGGTGGGAGGATTG[A/C]TTGAGCCCAGGAGTT	2186
rs756383102	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67932981	GATCAGCCAGGCGCA[G/T]TTGCTCATGCCTGTA	2186
rs756391006	snp	C/G			intron-variant, utr-variant-5-prime	BPTF	GRCh38.p7	17:67888850	GCTGTCTGTTACTGG[C/G]GTTGGGTTGCTGGGG	2186
rs756452226	snp	C/G	1.65121e-05	0.00287329	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67922986	ATCAGGGCATTTGCT[C/G]AGAGGTAAGGAAATG	2186
rs756455593	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67934945	CATCAAATATGTAAT[G/T]ACAAAACAATTCTCA	2186
rs756497315	snp	A/G	1.80305e-05	0.00300249	intron-variant	BPTF	GRCh38.p7	17:67928315	ATTGTTTTTATTTAG[A/G]ACTATTTTGATTCAT	2186
rs756498408	snp	A/G	4.95152e-05	0.00497545	missense, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67886160	TGTGAGAGCAGTAAC[A/G]CTAGTGCTACCACTA	2186
rs756499381	snp	C/G	6.62e-05	0.00575288	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912385	AACTACCGAGATAGC[C/G]TTGAGACCCTGCCAT	2186
rs756529581	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67905998	GGCACATGTATACAT[A/G]TGTCACAAACCTGCA	2186
rs756530563	snp	C/G	2.00395e-05	0.00316533	intron-variant	BPTF	GRCh38.p7	17:67909542	TAAAGTGCTAATACT[C/G]TGGAAATAACGTAAA	2186
rs756533047	snp	C/T	5.09213e-05	0.0050456	intron-variant	BPTF	GRCh38.p7	17:67886114	TTTAAAAATCAGATA[C/T]TCTATTTTTCTAGAA	2186
rs756536109	in-del	-/GAA	3.32121e-05	0.00407492	cds-indel, nc-transcript-variant	BPTF	GRCh38.p7	17:67903856	AAAGAGAAGAAACAG[-/GAA]GAAGAAGAAACGATG	2186
rs756540490	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67908826	AGTTGTCACTGACAA[-/T]TTTTTTTTTTTTTTT	2186
rs756541780	snp	A/G	4.94205e-05	0.0049707	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67854640	CTGTGTAGCACACAA[A/G]GTGCCTGGTGTGACT	2186
rs756552475	snp	A/G	1.65869e-05	0.00287979	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912482	TTAATCAGGTAGAAG[A/G]TATGGAAATAGAAAC	2186
rs756597953	snp	C/G/T	3.30307e-05	0.0040638	missense, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67886286	GGAGAAAGAGAATCT[C/G/T]ATACACCTGTCTCTA	2186
rs756648843	in-del	-/AGTGTTCATTTTTCCAACTGA			intron-variant	BPTF	GRCh38.p7	17:67916272	AGCTTTCTCTTTCAC[-/AGTGTTCATTTTTCCAACTGA]ATGCTGTCAATAGAA	2186
rs756652990	snp	C/T	3.45143e-05	0.00415403	synonymous-codon, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67891848	TCATTTGACAGTAGG[C/T]GATTTCAAATCGGAG	2186
rs756656069	in-del	-/AT			intron-variant	BPTF	GRCh38.p7	17:67858771	AGTGAAATTTAGTCC[-/AT]GCTCCAATTCTCCCA	2186
rs756660271	snp	A/G	2.16546e-05	0.00329042	intron-variant	BPTF	GRCh38.p7	17:67854793	CTTAATTTTTTGTAT[A/G]CATTTAAAATTAGAC	2186
rs756700760	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67855806	AAAAAATCTGGTAGG[A/G]TGAAATGAATGTCAG	2186
rs756713504	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67938841	AAAAATATGTATTAA[A/G]TAAGTAGGAAAAGAA	2186
rs756726022	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67834544	TGTCTGTTTCTCCTT[G/T]AAGTTCTAGCAATCT	2186
rs756747560	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67870495	ATTCCCGATTAAAAC[A/G]CCAGTTCACCACTGT	2186
rs756765238	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67872363	TTCATTAAATGGCAC[C/T]GGGAAAGTAGGGAGG	2186
rs756786663	in-del	-/T	1.80081e-05	0.00300062	intron-variant	BPTF	GRCh38.p7	17:67875525	ATTTTAAAGAATATC[-/T]TTTGAAGTTTTGTTG	2186
rs756807027	snp	C/T	6.66511e-05	0.00577244	synonymous-codon, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67875686	TCTCTCAGAAACCCC[C/T]GATAGCAGCAACATG	2186
rs756811636	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67902617	AGTGCAGTTAATAGG[C/T]ATGAGCTGTCAGCCT	2186
rs756813474	snp	A/T	1.70214e-05	0.00291726	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67903804	GTTACACCGGATGAC[A/T]TCAATTGAAAGAGAA	2186
rs756855574	snp	A/G	1.6768e-05	0.00289546	intron-variant	BPTF	GRCh38.p7	17:67919978	GTCTCTGAGTATTTC[A/G]GTTGGTTATTAATAC	2186
rs756862109	snp	C/T	1.64727e-05	0.00286986	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67854187	CATGGCAGAGATGCA[C/T]GTTGTGCTTTTGAAA	2186
rs756868616	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67856824	CCTCAGTTTTTTGTA[C/T]AGTACCTTTGTTCAC	2186
rs756874415	in-del	-/GAGT			intron-variant	BPTF	GRCh38.p7	17:67933242	CAGCCTGGGCAAAAA[-/GAGT]GAGACTCCGTCTGAA	2186
rs756883383	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67890184	AATTTACTGGTTTTG[A/G]TAGAAATACATCAAA	2186
rs756897689	snp	A/G	4.94181e-05	0.00497057	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67854062	GAGCATATAATGAAT[A/G]TCATTGCCATTTACG	2186
rs756903709	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67903381	TTTTTAATTCCTTAA[A/C]AAAATCTGTATATTT	2186
rs756908416	snp	A/G	1.66718e-05	0.00288715	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912083	CTGAAAAGAAAGGAC[A/G]GAGAACAAGTACATT	2186
rs756910471	in-del	-/TCGAG			intron-variant	BPTF	GRCh38.p7	17:67923152	CTCTGCCTCCCAGGC[-/TCGAG]TCGAGTGATCCTCCC	2186
rs756910571	snp	G/T	1.65583e-05	0.00287731	intron-variant	BPTF	GRCh38.p7	17:67920166	ATAGAATTCTATTCT[G/T]TCATGATTAACCTGT	2186
rs756947502	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67938470	AAACTTGTACTACCA[A/G]TTGTTAAAGCTATTA	2186
rs756970884	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67840106	TGGAAAAATACTGAT[A/T]TTTTTTTTTTTTTTT	2186
rs756996654	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67939343	ACAGATGGAAAAAAG[A/G]CAGCGAGTAAATATT	2186
rs757005833	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67828799	TCCCAAAGTGCTGGG[A/T]TTACAGGCATGAGCT	2186
rs757039651	in-del	-/TAAA			intron-variant	BPTF	GRCh38.p7	17:67921533	CCATTTCCAAGTAAA[-/TAAA]TAAATAAATAAATAA	2186
rs757039710	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67891388	CCCTAGTGGAAAATT[C/G]ATGACATTTATGTTT	2186
rs757098458	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67831230	AGGCCTTGACACATA[A/G]ATGTGTAGAGAGAGG	2186
rs757112658	snp	C/T	1.68394e-05	0.00290162	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67912225	TATAAATAAAATAAT[C/T]CCTGAGAATGATATT	2186
rs757113706	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67871091	TGCTTCATTTCTAAT[A/G]TATAACTCTCTGGTT	2186
rs757118247	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67943498	CCCTTTTTGGTAACT[G/T]CTCAGACCTTAGTGA	2186
rs757118310	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67974037	TATTTCTTAGGTATT[C/G]TAGTACTTTTATTTA	2186
rs757145349	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67926283	CAAAGTGCTGAGATA[A/G]CGAGCACCACTGCAT	2186
rs757152086	snp	A/G	1.64846e-05	0.0028709	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67893539	ATAAGCACCAGCACA[A/G]AGAAGACCATGATAA	2186
rs757176167	snp	A/G	1.6534e-05	0.00287519	missense, utr-variant-5-prime, nc-transcript-variant	BPTF	GRCh38.p7	17:67893427	ACCAAAAAGGAAGTG[A/G]TCATGAAAGGAAATA	2186
rs757193610	snp	C/T	1.69608e-05	0.00291206	intron-variant	BPTF	GRCh38.p7	17:67866719	CTCATTTTATTTTTG[C/T]TAAGTCTGAGCTAAA	2186
rs757231253	in-del	-/A			intron-variant	BPTF	GRCh38.p7	17:67884954	ATAGTTTTATTTTAC[-/A]TTTCTCATAGTTTGA	2186
rs757240673	snp	A/G	1.64819e-05	0.00287066	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67929351	GCGTTGTTCAAGTAC[A/G]GCAGAAAGTCCTGGG	2186
rs757268232	in-del	-/AAA			intron-variant	BPTF	GRCh38.p7	17:67932963	TGGCTTAAAGGTAAA[-/AAA]GATCAGCCAGGCGCA	2186
rs757294975	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67934333	GACTAGCCTGGCCAA[C/G]ATGGTGAAACCCCTT	2186
rs757381957	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67852024	CAGTGGCATATTCTA[A/T]ATACACTTCTGTGAA	2186
rs757382833	snp	G/T	0.000264686	0.011501	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911870	AAGATGTTGAAGTCT[G/T]GGAGCCGTTAAAGTG	2186
rs757390320	in-del	-/CTTC			intron-variant	BPTF	GRCh38.p7	17:67853359	TTCTCCTCCTCTGCA[-/CTTC]CTTCCTTTCTGTCTT	2186
rs757398703	in-del	-/T	1.68009e-05	0.00289831	intron-variant	BPTF	GRCh38.p7	17:67919967	TACCTTTTTAGTCTC[-/T]TGAGTATTTCAGTTG	2186
rs757401235	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67899068	CAATTTTGTTCCACG[A/C]TGAACTCCACCAAAA	2186
rs757404586	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67935660	CAGGAGTTCAAGACC[C/T]GCCTGCCCAACGTGG	2186
rs757411740	snp	C/T			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67887270	GCTTATTCATATCTT[C/T]TTCTCACTTTTTCCT	2186
rs757437994	snp	A/G	1.67223e-05	0.00289151	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67909658	AAAAAAAATAAAAAT[A/G]GAGCCTGATTCTGAA	2186
rs757482601	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67837195	TTAAAAAAACTAGTC[C/G]TATTGAGAATTCAGG	2186
rs757510296	snp	A/C	1.65299e-05	0.00287483	missense, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67886293	GAGAATCTCATACAC[A/C]TGTCTCTATTCAGGA	2186
rs757520968	in-del	-/A	0.00153246	0.0276384	frameshift-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67909643	ATGTTCACGAAGTCC[-/A]AAAAAAATAAAAATA	2186
rs757520986	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67865414	CCTTATCATTATACC[-/T]TTTAAGTCTTATAGT	2186
rs757529804	snp	G/T	1.64765e-05	0.00287019	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67928435	AACCAGCACCATCTC[G/T]CCAGCACAGAAGGTT	2186
rs757537772	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67917747	AATTGATTCTCCTGC[C/T]TTAGCCTCCCAAGTA	2186
rs757555219	snp	C/G	1.7863e-05	0.00298851	intron-variant	BPTF	GRCh38.p7	17:67928324	ATTTAGAACTATTTT[C/G]ATTCATGTTTCCTCT	2186
rs757610265	snp	A/G	1.65968e-05	0.00288065	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912492	AGAAGATATGGAAAT[A/G]GAAACCTCAGAAGTT	2186
rs757620413	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67860538	GAAGCCAAGACATAT[A/T]CAGCATATAACTCAG	2186
rs757639983	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67863819	TCTTCATTTCTATGG[G/T]TTTGTTTAGAAACGA	2186
rs757649392	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67874626	AGAGGTGAAGGTACA[C/G]CAAATTGATTGAATT	2186
rs757688706	snp	G/T	1.68156e-05	0.00289957	missense, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67891866	TTTCAAATCGGAGAA[G/T]TCCAACGGGGAGCTA	2186
rs757692330	snp	G/T	3.31301e-05	0.00406989	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911439	GAAACAAAATTCCAT[G/T]GAAAATGACATAGAA	2186
rs757694877	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67906971	GGAGGATCAGTTGAG[C/G]CCAGGAGTTCAAGAA	2186
rs757724877	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67880287	TCTCCAAATTAATTT[A/C]TGGTCTTAGTATTTT	2186
rs757748147	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67906026	GCACGTTGTGCGCAC[A/G]TACCCTAGAACTAAA	2186
rs757771109	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67930994	TAGCTGGGCCGGATG[C/T]GGTGGCTCACACCTG	2186
rs757784710	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67895108	AGTTTTTAAAATATA[A/G]ATACAAGCCAGGCAC	2186
rs757795135	snp	A/G	3.29843e-05	0.00406092	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67866570	GATTATTGGGAAGCA[A/G]AACTCTGCAAAATTC	2186
rs757796037	snp	C/G	0.000200622	0.0100135	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	BPTF	GRCh38.p7	17:67825563	TCCGGAGTGGGGCCC[C/G]AGCAATTCGGATTGA	2186
rs757845222	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67964869	CTGGGCGTGGTGGCG[A/G]GCGCCTGTAGTCCTA	2186
rs757851453	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67845098	GTGATAGGAATGCTG[G/T]ATAAGTGCACGTCTC	2186
rs757898951	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67891476	TTAAACCTTTTTATA[A/C]AGAAATCCATATTGA	2186
rs757904494	snp	A/G	1.65737e-05	0.00287864	intron-variant	BPTF	GRCh38.p7	17:67920171	ATTCTATTCTTTCAT[A/G]ATTAACCTGTTAACC	2186
rs757916067	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67939434	AGCTACCAAAAAATT[A/T]TTCTTAGCAACTGTT	2186
rs757933465	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67901795	GGCTTTATGATTGCA[C/T]TGTTCTGAAGAGTAG	2186
rs757950224	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67904638	TAAAAATGCATAAAA[A/C]CACATGTGGTTTATA	2186
rs757954448	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67976756	GCTGATGATTGTCAC[A/C]GGACTTTAAATTCTA	2186
rs757971841	snp	C/T	1.6473e-05	0.00286988	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67854237	ACACTTCCAATACTA[C/T]CTTTGGACCTGCTGA	2186
rs758003464	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67839257	TGATGCGAATATTTC[A/G]TGGTTAACTGTGGGT	2186
rs758015766	snp	G/T	1.68272e-05	0.00290057	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912235	ATAATCCCTGAGAAT[G/T]ATATTAAATCATTGA	2186
rs758056681	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67953047	CTCACTGCAAGCTCC[A/G]TCTCCCCGGGTTCAC	2186
rs758069198	snp	C/T	1.64999e-05	0.00287222	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67910986	TTGTCAGGAGAGTTC[C/T]CAAGTAGATGTGGTC	2186
rs758102335	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67867031	ATTTAAAAAGGTAAT[A/G]CGTATAATCTTATGT	2186
rs758128646	snp	A/G	1.65173e-05	0.00287374	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67893437	AAGTGATCATGAAAG[A/G]AAATATCAACAATTA	2186
rs758155622	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67879975	GCAGGACAAACATCT[A/G]AACTATCCAAACTAC	2186
rs758159189	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67926697	CAACTTTGAAGGCAT[A/G]TCCTCCTATAAATAA	2186
rs758166560	snp	C/T	1.64765e-05	0.00287019	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67929382	TATCATTCCATCAAG[C/T]ACAGGTACCAGTCAG	2186
rs758215391	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67829708	ATGATTGATGAGTTT[C/G]AATCCTGTTGTACTG	2186
rs758219850	snp	A/C	3.40298e-05	0.00412477	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67929479	GGAGGAACCACAAGC[A/C]ATTCACAAGTAAGAA	2186
rs758241703	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67865837	AAGCTCCTCTTCTCT[C/G]CAGTTTGGGCTTCGA	2186
rs758247503	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67895820	TTTGACAAAAACAAA[A/G]TTAAAAATGCAATTC	2186
rs758267480	snp	A/G	1.66286e-05	0.0028834	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911143	ATCAAGTTGGAGGGT[A/G]GAATTAAGGGTATAG	2186
rs758269665	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67899320	TTTATGCTGCAGTCA[C/T]GCCAGATACCTTGAT	2186
rs758269933	snp	A/C	1.65395e-05	0.00287567	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67874972	TCCCTTGAAAAAGAC[A/C]GTGACGACAAAACAC	2186
rs758272876	snp	A/T	1.68428e-05	0.00290192	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67913140	AAAACCTGCTTTGGA[A/T]ATATGGCCATATCCT	2186
rs758289818	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67955807	ATGACGGAATGAGAC[C/T]CCATCTCGAAACAAA	2186
rs758303195	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67900889	TCTTGCTTGCCTGTA[A/G]TGCCAGCTGCTTGGG	2186
rs758305005	snp	A/G	1.66676e-05	0.00288679	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67874843	GAATCCATAAGAGCC[A/G]AAAAGGGAGACATTG	2186
rs758332344	snp	C/G	5.00163e-05	0.00500056	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67826267	GGAGGAGATGGAAGA[C/G]GACGACGACGACGCC	2186
rs758360738	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67935926	TATACATACTTAGGA[C/T]GTAAATCTATTTGAA	2186
rs758388744	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67939660	AGGCGGGTGGATCAC[A/G]AGGTCAGGAGATCAA	2186
rs758412810	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67913193	TCACTTGGAGGTATG[C/T]ACTTTAAAATGTATT	2186
rs758428413	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67892483	ACTGTGGATAGGACA[A/G]CATGGCATCCCAGCT	2186
rs758442395	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67919315	CCAAGGCAGGAGGAT[C/T]ACTTGAGGCCAGGAG	2186
rs758446089	snp	A/T	1.66551e-05	0.00288571	missense, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67891877	AGAAGTCCAACGGGG[A/T]GCTAAGTGAATCTCC	2186
rs758447818	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67922574	GCTCATAAGCCTTGT[A/G]TTTTGGGGGTCAGCA	2186
rs758450632	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67870756	ACCTCTCAAAGAAAA[C/T]GCTTCATTTCTTTTT	2186
rs758457228	snp	C/T	0.000132343	0.00813351	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67874977	TGAAAAAGACAGTGA[C/T]GACAAAACACCAGAT	2186
rs758488534	in-del	-/A	1.65605e-05	0.0028775	intron-variant	BPTF	GRCh38.p7	17:67923007	AAGGAAATGGTTAAT[-/A]ACCTGGTCAGCTATT	2186
rs758499462	snp	A/T	1.71393e-05	0.00292734	intron-variant	BPTF	GRCh38.p7	17:67866427	ATAAGTGGCATTATG[A/T]CTAACATATAAAGTA	2186
rs758524767	snp	G/T	3.45925e-05	0.00415873	intron-variant	BPTF	GRCh38.p7	17:67909793	GTGGAGGGCAGCCTG[G/T]GGGTGATAAGAATGC	2186
rs758540250	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67920626	ATAGGCACTGGGTGG[C/T]AAATACATAGAAGAA	2186
rs758544969	snp	A/G			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67887750	GGTATCAAACTCTTT[A/G]TTTTCCTCTCTCTCT	2186
rs758547212	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67876081	TGTTGAATGATCTGA[C/T]CTTTCCAGTTCTGTA	2186
rs758551555	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67860783	GGCTGGTCTCGAACT[C/G]CTGGGCTCAAGTGAT	2186
rs758556201	snp	C/T	3.29549e-05	0.00405911	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67928462	GGTTATGGTGGCCCC[C/T]ATAAGTGGCTCAGTT	2186
rs758568290	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67837313	TCCTAGGACTGGGAT[A/T]GGATTGTTGCATTAT	2186
rs758596421	snp	C/T	3.46027e-05	0.00415934	synonymous-codon, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67892019	AGCAAATAAATTATT[C/T]AAGGAGGGCAAAGAG	2186
rs758596683	snp	A/G			upstream-variant-2KB	BPTF	GRCh38.p7	17:67823710	GAATGCATTTCTCTG[A/G]CAATTAGTGCTTGTA	2186
rs758634870	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67907943	GATCCTTTTTTTCAG[G/T]CTTTTATTCTGTTAT	2186
rs758644344	in-del	-/ACAA			intron-variant	BPTF	GRCh38.p7	17:67842988	GGAAAATGTAAAAAC[-/ACAA]ACAGTTGTTTCTTAA	2186
rs758649387	snp	C/T	4.94645e-05	0.00497291	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67866578	GGAAGCAGAACTCTG[C/T]AAAATTCTAGAAGAA	2186
rs758715601	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67845213	GAATCATCCCTGTAA[A/T]GGTATCTTTCACCTT	2186
rs758753172	snp	A/G	1.69579e-05	0.00291182	intron-variant	BPTF	GRCh38.p7	17:67928604	CAGTCAAATTCAGGT[A/G]TGGAACTATCATTAA	2186
rs758762224	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67846709	GGACTTGTGTGGGTT[G/T]GTTTGTTTGTTTGGA	2186
rs758801749	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67870458	AGTGTATTGGTAATG[A/G]ATTGAGCATTCAAAT	2186
rs758828568	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67881987	TTACAGGCGCCCACA[A/G]CCACACCCAGCTAAT	2186
rs758866518	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67932227	AAGTATGCTTATTAA[A/G]AATGTAACAGAAATC	2186
rs758880028	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67895222	CCTGTAGTCCCAGGT[A/T]CTCGGGAGGCTGAGG	2186
rs758887059	snp	C/T	0.000214622	0.0103569	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67920022	CACCATAGAAACATC[C/T]GAAACTGAAATCACA	2186
rs758887861	snp	C/G	0.00144571	0.0268471	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	BPTF	GRCh38.p7	17:67825595	CCTTCTCCCTCCACC[C/G]GCTTCCGTCGGCCGG	2186
rs758907715	in-del	-/C			intron-variant	BPTF	GRCh38.p7	17:67859541	CCCAAGACCCTGTGG[-/C]TCTTAGGAGGTAGAA	2186
rs758921762	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67931209	GGCGGAGGTTGTAGT[A/G]AGCCAAGATTGTGCC	2186
rs758940396	snp	A/G	3.73965e-05	0.00432398	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67826163	TCCGAGGAGGAGGAG[A/G]AGGAGGACGGCGACG	2186
rs758958385	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67907848	TAATAATCTGATTCT[A/C]AGTCCATATTCCACT	2186
rs758989799	snp	C/T			upstream-variant-2KB	BPTF	GRCh38.p7	17:67824838	AGTGCGGATTCCACG[C/T]TACAGGTCTTAGGGC	2186
rs759027875	snp	A/G	1.64738e-05	0.00286995	intron-variant	BPTF	GRCh38.p7	17:67891816	TACTTATTGTCAGCA[A/G]TTGCTTTGTGGCCTA	2186
rs759074003	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67894916	TTGTGACTTGAATCT[A/G]CTTTTTAGCCCTGAT	2186
rs759075003	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67921562	AAATAAATAAAAAGA[A/T]AATGTCCTTAGATAG	2186
rs759077186	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67861150	ATTACTGTCCCACCA[A/G]CTGCTCAAGCTAGAA	2186
rs759103454	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67832017	CTGCCTCAGCCTCCC[G/T]AGTAGGGGACTACAG	2186
rs759152445	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67930203	ACATATTAGATACAT[C/T]ATTTCTTTTTTTGAG	2186
rs759157712	snp	A/G	0.000269599	0.0116072	intron-variant	BPTF	GRCh38.p7	17:67854771	TCATAATGTAAGTAA[A/G]TCTGGTCTTAATTTT	2186
rs759164154	snp	C/T	1.66576e-05	0.00288592	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67912588	TGAAAATGGTCTGCC[C/T]ATCAACAAAAATGAA	2186
rs759170572	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67863087	ACAAATGGGGTGGCT[G/T]GAAAAAATATGAATT	2186
rs759197596	snp	C/T	1.65312e-05	0.00287495	synonymous-codon, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67891929	TGGCTCAACTCGAAT[C/T]ATCACCAGATTGCGG	2186
rs759212766	snp	C/T	1.66346e-05	0.00288393	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67866509	GAAAATTTGGTATTA[C/T]AGCACAAAGGTCCAA	2186
rs759224979	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67934260	CTGTGGCTCACGCCT[A/G]TAATCCTAGCACTTT	2186
rs759259942	snp	C/T	0.000377572	0.0137348	upstream-variant-2KB	BPTF	GRCh38.p7	17:67825499	GGCCGCTGTCGGTTC[C/T]CCCAGTCACCGAGCG	2186
rs759276063	in-del	-/TCTCT			intron-variant	BPTF	GRCh38.p7	17:67906654	ACGGTTTCTTTGCAC[-/TCTCT]TCTCTTTCTTCAGCC	2186
rs759277757	snp	G/T	1.66125e-05	0.00288201	intron-variant	BPTF	GRCh38.p7	17:67932051	CATTATCATTTTACA[G/T]CTCAACAGCCAGTCT	2186
rs759287838	snp	G/T	1.65633e-05	0.00287774	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911520	AACAAAAGGAAATGA[G/T]TTTTTCATCGATGAC	2186
rs759298289	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67884246	AAGTAGCTGGGATTA[C/T]AGGCATGCACCACCA	2186
rs759298357	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67869224	GTCCTCTAAAAGGCA[A/G]TGTGAGATAGGATTT	2186
rs759306365	in-del	-/GAGGAGGACATGGTCTCCGAGGAGGAGGAG	6.38111e-05	0.00564814	cds-indel, nc-transcript-variant	BPTF	GRCh38.p7	17:67826133	GAGGAGGAGGAGGAA[lengthTooLong]GAGGAGGACGGCGAC	2186
rs759330111	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67834095	CATCCATCACCTTCT[C/G]CAGCCTGCCTTCTCT	2186
rs759338697	snp	A/G	1.6571e-05	0.0028784	intron-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67918854	GTAAGGGGGAAGGGA[A/G]TTATTTTCTAATTTA	2186
rs759349650	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67882858	TAAAAATTAGCTGGG[C/T]GTGGTGGTGCTTGCC	2186
rs759379179	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67915912	ACTTACCGTGCATGT[C/G]GTGTGTTCCTCCCTG	2186
rs759411449	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67847452	CGGGGAGGCAGAGCT[C/T]GCAGTGAGCAGAGGT	2186
rs759444142	snp	A/G	1.6473e-05	0.00286988	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67894106	TTTAGCCATTTTGGA[A/G]TGTGCAGTTAAACCA	2186
rs759447434	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67916895	ACCATAATCAACCAC[G/T]AAGTTCATTTAAGTA	2186
rs759485273	snp	C/T			utr-variant-3-prime	BPTF	GRCh38.p7	17:67982817	GGTAAAAGTACAAGA[C/T]GACCTCTAGATGTCT	2186
rs759491182	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67903061	AGAAGGAGTTGTGGC[C/T]GATGCCTGTGTCTCA	2186
rs759497325	snp	A/T	1.81444e-05	0.00301195	intron-variant	BPTF	GRCh38.p7	17:67903745	TTTATCTTTTCTGTT[A/T]ATTTTTCCAAGTTAA	2186
rs759522234	in-del	-/CTGTATCTTCTTCTC	1.69215e-05	0.00290869	intron-variant	BPTF	GRCh38.p7	17:67866716	TTCTCATTTTATTTT[-/CTGTATCTTCTTCTC]TGTTAAGTCTGAGCT	2186
rs759539151	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67856199	GGGTATTTGTATGTG[G/T]TCAGTTTTTTAAGAT	2186
rs759560898	snp	A/T	1.65806e-05	0.00287924	missense, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67875657	CCCTCTGAAGGGAGG[A/T]GCCCTGTGGGGTGTC	2186
rs759563901	in-del	-/AG			intron-variant	BPTF	GRCh38.p7	17:67958345	TCAAAAAGAAAAAAC[-/AG]AGTACAGTAAAGAAG	2186
rs759614817	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67970210	TGCACTCCTCCAGCC[C/T]GGGCAGCAAGAGTGA	2186
rs759614953	snp	C/T	4.97401e-05	0.00498674	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67929461	CCCAATACCTCAGGC[C/T]CTGGAGGAACCACAA	2186
rs759624823	snp	C/T	1.67041e-05	0.00288994	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911198	AAAATCTCTCTGAAT[C/T]ACCAGTAATAACGAA	2186
rs759643114	snp	A/G	1.66396e-05	0.00288436	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912328	GAAAGAAACAGCTCC[A/G]AAACAAAATCGCATT	2186
rs759652020	snp	A/G	9.9481e-05	0.00705199	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911117	TGGAAGAAAAACAGC[A/G]ACTCGAAAAAATCAA	2186
rs759696294	snp	C/T	8.25021e-05	0.00642217	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67929337	CATCTTTTTTTAAGG[C/T]GTTGTTCAAGTACAG	2186
rs759703286	snp	C/T	1.64768e-05	0.00287021	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67893510	TCAATACTCCACCAA[C/T]TCATTTGCTTTGAAT	2186
rs759710811	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67933662	TAAAGTGTAAAAAGC[A/G]AAACTATTTGAAATC	2186
rs759723827	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67896309	TGATGGACTGTTACA[C/T]AGCAGTGAAAAACAC	2186
rs759724914	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67924729	TTTTTAGCCAAATTC[A/T]TGCACACCCATGCAC	2186
rs759750201	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67923771	AAGTGTGAGCCACCG[C/T]GCCCGGCCCTCTCTC	2186
rs759753871	snp	C/T	1.64727e-05	0.00286986	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67854493	AGGGGTGATACAGTA[C/T]GATGACCATTGTAGG	2186
rs759801577	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67925564	GTGCCTAAACATTGA[C/G]GACCTGAATAAAAGA	2186
rs759821078	in-del	-/TTAG			intron-variant	BPTF	GRCh38.p7	17:67869691	ATGTACTTTTAAAAA[-/TTAG]TTAAACCGGCAGGGC	2186
rs759836896	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67829307	TTGCAACACATTATT[G/T]TTAAAGATTATGGTA	2186
rs759852569	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67850437	GCAGTAGCATGATCT[C/T]GGCTCACTGCAACCT	2186
rs759852975	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67842048	AAATGTAAAATAAAA[C/T]GTAAAAGTATTGCAA	2186
rs759873248	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67878635	TACTGTTCTTTGCAC[C/T]TGCTAGCTCCCTTGT	2186
rs759874124	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67828385	GACATTTTGGCAGGA[C/G]AGTTCAGCTAACTTT	2186
rs759885749	in-del	-/GTTTA			intron-variant	BPTF	GRCh38.p7	17:67830706	GTCTCAAGTAACTCG[-/GTTTA]GCAAGAGCCTGAGTG	2186
rs759896905	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67885914	TTGGGTCCTCACCCC[A/C]CCAAAAAAAGTCAGT	2186
rs759947914	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67844819	CATGATCTCGGCTCA[C/T]CGCAACCTCTGCCTC	2186
rs759956295	in-del	-/CTTG			intron-variant	BPTF	GRCh38.p7	17:67840458	GTTGCTGCTGCTCCT[-/CTTG]TTGTTGTTGTTGCTG	2186
rs759961156	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67865390	GTGTGCCCAGGCACT[A/G]TGGTAGATGCCTTAT	2186
rs759962872	snp	C/T	1.65422e-05	0.0028759	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67874914	TGAGACTGAGAATGA[C/T]TCTAAAGATGCTGAG	2186
rs759969670	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67973214	CCCGTCTCTACTAAA[A/C]ATACAAAAAATTAGC	2186
rs759971975	snp	A/G	1.65184e-05	0.00287384	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67913034	TTACCAAGAGCAGCA[A/G]GAAGAGCATTTTTGT	2186
rs759972504	snp	A/G	1.73228e-05	0.00294297	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67909600	AAAATAATATGGATG[A/G]AAATATGGATGAGTC	2186
rs760022493	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67900224	ATTCTCCTGCCTCAG[C/T]CTGCTGAGTAGCTGG	2186
rs760023134	snp	A/G	1.82045e-05	0.00301694	intron-variant	BPTF	GRCh38.p7	17:67913204	TATGTACTTTAAAAT[A/G]TATTTGGGGGAGGGA	2186
rs760025411	snp	A/G	1.64803e-05	0.00287052	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67911736	GGGATGTGACTCTGA[A/G]TCTAATAGCACTTTG	2186
rs760048942	snp	A/T	1.64923e-05	0.00287156	intron-variant	BPTF	GRCh38.p7	17:67909535	GACATATTAAAGTGC[A/T]AATACTCTGGAAATA	2186
rs760083334	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67851566	TGGTAGGAGAGAAGA[C/T]ATTAGTATAAGGCAT	2186
rs760097233	snp	C/T	1.65026e-05	0.00287246	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67928555	ACAAAACAAGAACTT[C/T]CATCAAACCTTTGCT	2186
rs760107035	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67910021	ATACCCATTAGCAGT[C/T]ACTTCCCAACCCCTC	2186
rs760133868	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67884632	TGTTGCCCAGGCTGG[G/T]CTCGAACCCCTGACC	2186
rs760169367	snp	A/G	3.33211e-05	0.0040816	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67912618	AAATGTCAATGGAGA[A/G]TCTAAAAGAAAAACC	2186
rs760172913	snp	C/T	1.65603e-05	0.00287747	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67866529	CAAAGGTCCAACTTG[C/T]AGAATTAATTGACTG	2186
rs760174078	in-del	-/A			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67888026	ATTGATGCCTCCAGC[-/A]AAAGTTGGGTAGGAA	2186
rs760196246	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67848396	GAGCCAGGGGGCATG[A/C]GTAATTGCCTGTAAT	2186
rs760211751	snp	A/G	0.00019181	0.00979122	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	BPTF	GRCh38.p7	17:67825541	ACAAGATGGCGGCTG[A/G]AGGCGATCCGGAGTG	2186
rs760247688	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67863223	TTCTGGCAGTCCTTA[A/G]CATTTCTTGGTTTAC	2186
rs760275783	snp	C/G	1.65556e-05	0.00287707	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911530	AATGATTTTTTCATC[C/G]ATGACTCTAAACTAG	2186
rs760291433	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67916113	CTTGGGACATCCCTG[C/T]ACTAGTTAACATTTC	2186
rs760297149	snp	A/C			missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67909718	AAAAGGAGCAGACCA[A/C]AATGAAATGGATATC	2186
rs760331868	snp	A/T	2.08244e-05	0.00322673	intron-variant	BPTF	GRCh38.p7	17:67893347	TGACATAAATAATGC[A/T]GTCTTTTTATTTTTT	2186
rs760367419	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67933653	ATGTCATATTAAAGT[A/G]TAAAAAGCAAAACTA	2186
rs760372683	in-del	-/TAATGT	0.00094594	0.0217273	cds-indel, nc-transcript-variant	BPTF	GRCh38.p7	17:67874860	AAAGGGAGACATTGA[-/TAATGT]TAAAAGCCCAGAAGA	2186
rs760386843	in-del	-/GTTT			intron-variant	BPTF	GRCh38.p7	17:67851812	GCATCCTTCCCAACA[-/GTTT]GTTTGGTTAAACTGT	2186
rs760387784	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67963520	CAGTGAGTTCTGATA[A/C]GAGCATCATATTTAA	2186
rs760396628	snp	A/G	0.000149824	0.00865387	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67826110	TGGTGTACGATGACC[A/G]CGAGAGCGAGGAGGA	2186
rs760401174	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67835500	GTGAAGTCCTCCTTT[A/G]TGGAGACTCTGGGCC	2186
rs760418716	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67916999	ATGCAGTTAAGTAAA[C/T]TTATTTTGAAATACG	2186
rs760426701	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67838359	CTAGTAAAACCTTTA[A/C]ATTTTATTTTTGCTT	2186
rs760436548	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67865162	AGCATTTCCTTTGAA[C/T]GGCATGTTGGCACTC	2186
rs760450599	snp	A/G	1.65023e-05	0.00287244	intron-variant	BPTF	GRCh38.p7	17:67903930	TCAGGTAATTTTTAC[A/G]ACAACCCTTTAAAAT	2186
rs760469019	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67905450	AGTGGCTTACACCTA[C/T]AATCCCAGTGCTTTG	2186
rs760486512	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67872906	GGGCAACATAGTGAG[A/G]CTCCATCTCTATTTT	2186
rs760509259	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67904201	GCCTGGCTAATTTTT[A/G]TATTTTTAGTAGAGA	2186
rs760539856	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67885500	GAGGCTGAGGCGGGA[G/T]AATCTCTTGAACCTG	2186
rs760569489	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67939956	CCTTCATGGCTCTCC[C/T]AAGCTATCTGTCAAA	2186
rs760605849	in-del	-/A	1.91992e-05	0.00309826	intron-variant	BPTF	GRCh38.p7	17:67892057	CTTTCTGTTTAAAAC[-/A]AAAATCTGTGGAATG	2186
rs760620027	snp	C/T	1.66205e-05	0.00288271	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67922843	TCCTTTCCAAAGAAA[C/T]GCCTACACCTCAGAG	2186
rs760625505	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67925051	TTGCACCCATCCAGG[-/T]TTTTTTTTTTTTTTT	2186
rs760626111	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67891301	ATGTTGAGAGGTCTT[C/T]ATTAGGTTATAAAAA	2186
rs760658045	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67904051	TTATTTATTTTGAGA[C/G]AGAGTCTCGCTCTGT	2186
rs760665857	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67857627	GTGTGCTACCATGCC[C/T]GGCTAATTTTTGCAT	2186
rs760712675	snp	G/T	1.64727e-05	0.00286986	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67854320	CCAGAGGTGCTGCGG[G/T]TGTACTGTGAGAGTG	2186
rs760749708	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67842228	ATATACATAGACATA[C/T]ATCTACATACATTGA	2186
rs760798341	snp	G/T	5.01107e-05	0.00500528	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911224	ACGAAAGCAAAAGAA[G/T]GGTGTCAGAGTGACT	2186
rs760810682	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67927576	ATGTTTTTATAGTTG[A/G]ATAAATTAATATTAC	2186
rs760814181	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67879632	TTGGCTATGTGGTTT[A/T]GCAGACTGTACAAGA	2186
rs760843607	snp	A/G	1.65337e-05	0.00287517	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67874963	GAAGACCAGTCCCTT[A/G]AAAAAGACAGTGACG	2186
rs760861315	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67878718	TCAGTCGTTTAGATA[C/T]CCTCTTTTGGGAGGT	2186
rs760874677	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67920577	CAAGAGGCATAAAGA[G/T]TTACTCAAAAAATGT	2186
rs760897073	snp	C/G/T	3.48385e-05	0.00417352	intron-variant	BPTF	GRCh38.p7	17:67826358	CACCCAGCCCAGTTG[C/G/T]TGCAGACTCCTTCCC	2186
rs760926138	snp	A/G			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67887028	TGCTGGTCAAATGGT[A/G]GCTACATTTAAAAAA	2186
rs760930361	snp	A/G	3.29766e-05	0.00406045	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911822	TTCAGAATAGCAATG[A/G]AAGCATTTCTGAACA	2186
rs760967430	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67854945	TTTAAGAAGGTAAAG[A/G]AAACATATATGAAAG	2186
rs760989101	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67836855	CTGTGCAAAGAGTAA[A/G]ATGTTTTAAGGTGGT	2186
rs760997819	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67830371	CTCTAAGGATTGTGA[C/T]ATTGGAGATCAGTGG	2186
rs761009133	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67901960	GTGATAGCAAAACAC[A/C]ACAAAACCCTGAGCA	2186
rs761042356	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67868055	TTTATTTCTATGAGT[A/G]TACATTCATGGATAT	2186
rs761058157	in-del	-/G			intron-variant	BPTF	GRCh38.p7	17:67895109	TTTTTAAAATATAAA[-/G]TACAAGCCAGGCACA	2186
rs761061981	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67935487	CAAGTAATAATAATT[A/G]CAAAACAGAAAAGAC	2186
rs761062746	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67900381	AAGTGCTGGGATTAC[A/G]GGCGTTAGCCACCGC	2186
rs761085604	snp	C/G/T	3.29491e-05	0.00405877	missense, nc-transcript-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67918814	GCGGCCAAGGCTCCT[C/G/T]CAGGAGGAGGGACTA	2186
rs761133458	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67867713	TTATGGGTTTTTCTC[A/T]TGGTTAGCCTAGGTT	2186
rs761138754	snp	C/T	1.65466e-05	0.00287628	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67911946	GCCGGTCAAGGGGAC[C/T]GAAGCAAATGGTAAA	2186
rs761153701	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67874343	TCTGTTTTCTCTTTT[C/T]ACAGTTGAGGAAATG	2186
rs761159904	snp	A/C	1.68635e-05	0.0029037	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67909635	AAAAGAAAATGTTCA[A/C]GAAGTCCAAAAAAAA	2186
rs761183218	in-del	-/TC	1.67461e-05	0.00289357	frameshift-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67912194	AAGTGGTAATGTTGA[-/TC]ACCAAAGGTTAATAA	2186
rs761183772	snp	A/G	1.64787e-05	0.00287038	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67928424	ACAAGCAGTACAACC[A/G]GCACCATCTCTCCAG	2186
rs761209128	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67942271	CAGCGAGCCAAGATA[C/T]ACCACTGCACTCCAA	2186
rs761211252	snp	C/G	3.39415e-05	0.00411941	intron-variant	BPTF	GRCh38.p7	17:67909773	CAAGGTAAGGAGAGT[C/G]AGCTGTGGAGGGCAG	2186
rs761226992	snp	A/T	1.65616e-05	0.00287759	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912841	TCTGTAAAGGAGCAG[A/T]GCAAAACCGTGGTCA	2186
rs761258437	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67936585	TCTCCAGGGTTTTGC[C/T]ACTTTTCTTCCCTGG	2186
rs761263717	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67907505	GGATTACAAGTACCC[A/G]CCACCACGCCGAGCT	2186
rs761282503	snp	A/G	1.65603e-05	0.00287747	synonymous-codon, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67891968	TAGCAAACTTAGTCA[A/G]CTGAAGAGCCAGCAG	2186
rs761292486	snp	A/G			synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67826132	CGAGGAGGAGGAGGA[A/G]GAGGAGGACATGGTC	2186
rs761312605	snp	A/G			intron-variant, utr-variant-5-prime	BPTF	GRCh38.p7	17:67888704	ATGACACTCATAAAC[A/G]TAGTAGAGGGTGTTC	2186
rs761313790	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67850071	TACTTACGTAGAAAT[C/G]AAAACACATTTCTAA	2186
rs761329055	in-del	-/TTTTTTAGCTTT/TTTTTTAGCTTTATTTGATCACTACATTT	5.01979e-05	0.00500963	cds-indel, frameshift-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67912187	GAGTAGTAAGTGGTA[lengthTooLong]ATGTTGAACCAAAGG	2186
rs761331009	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67933825	GCACTCCAGGAGGCC[A/G]AGATGGGCAGATCAC	2186
rs761333658	in-del	-/G			intron-variant	BPTF	GRCh38.p7	17:67970096	AAAGTAGCCAGGCGT[-/G]GTGGCACATGCCTGT	2186
rs761380956	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67885772	AGCAAACTACCTCTG[C/T]AATATCTGGCGCACT	2186
rs761408844	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67836583	CCTAAAACAATCCTT[C/T]CTAAAGGTTTATGAA	2186
rs761435531	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67873103	GTAAAAAATAAATTT[A/G]TAAAAAAGGAAACAC	2186
rs761454463	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67917281	GGGATTACAGGCGCC[C/T]GCCACCATACCCAGC	2186
rs761469650	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67959298	GCTCATCTTTCAGTC[A/G]GCTCTCCTTTGAAGA	2186
rs761471003	snp	A/G/T	4.99125e-05	0.00499542	intron-variant	BPTF	GRCh38.p7	17:67904868	AATTACATGTCCTGC[A/G/T]TAATCGTTTCTGCTT	2186
rs761505916	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67918342	TAATAACAATTATCT[A/G]TTTCTCTATATTTGG	2186
rs761527186	snp	A/G	1.64738e-05	0.00286995	intron-variant	BPTF	GRCh38.p7	17:67886086	AATTCGTCATTTTTC[A/G]TGTGATTTCCAATTT	2186
rs761534398	in-del	-/G			intron-variant	BPTF	GRCh38.p7	17:67898677	TTTTTTTTTTTTTTT[-/G]AAGATGTATTGCAAA	2186
rs761545241	in-del	-/ATAA	0.000657448	0.0181188	intron-variant	BPTF	GRCh38.p7	17:67893336	ACATCTTTGATTGAC[-/ATAA]ATAATGCAGTCTTTT	2186
rs761568509	snp	A/G	1.64806e-05	0.00287054	missense, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67886233	AACTAAATTCTTCCC[A/G]GAGTGAATCTGCTAA	2186
rs761588831	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67894684	ATCAAAAGAGATCTG[G/T]TATATGAAAATTTAA	2186
rs761613293	snp	A/T	1.65949e-05	0.00288048	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911126	AACAGCGACTCGAAA[A/T]AATCAAGTTGGAGGG	2186
rs761621400	snp	C/T	8.23608e-05	0.00641667	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67854502	ACAGTATGATGACCA[C/T]TGTAGGGTTTGTCAC	2186
rs761632961	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67905600	TGTGGTCCCAGCTAC[C/T]TGGGGGTCTGAGGCA	2186
rs761633219	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67859982	GGAAATCAAATATTT[G/T]ATTTTTCTTAGTGGA	2186
rs761695656	snp	A/G	1.6483e-05	0.00287076	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67922894	CACTGCGGCCAAAGA[A/G]ACCAGAAACGCCCAA	2186
rs761724085	snp	C/T	4.96496e-05	0.0049822	intron-variant	BPTF	GRCh38.p7	17:67924531	TTCTGATAAGTTTCT[C/T]CTTTTTTTCCTGCAG	2186
rs761743451	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67879872	GAGAGCATTAATCTG[C/T]TCTTGAGGGATCCGT	2186
rs761746961	snp	G/T	3.31516e-05	0.0040712	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912358	TTGCTGAGTTCTTCA[G/T]ATGCTGAAGGTAACT	2186
rs761777454	snp	A/G	1.65392e-05	0.00287564	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912418	ACCAAAGAGTCTGAC[A/G]GTACACAGACGACCA	2186
rs761785841	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67844879	CTCCCTAGGAGCTGG[G/T]ATTATAGGCATGTGC	2186
rs761791364	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67900486	CTGTAATCCCAGCAC[A/T]TTGGGAGGTGAAGCG	2186
rs761822653	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67831445	AGTAGAGAGGTGTGT[C/T]CTAGGTATGCATTAA	2186
rs761831796	snp	A/G	1.66106e-05	0.00288184	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67854726	GATATGATAGAAGTC[A/G]GAGGAAATACTGGTT	2186
rs761851451	snp	C/G	1.64933e-05	0.00287165	missense	BPTF	GRCh38.p7	17:67932017	CTGTGATGGTACAGC[C/G]AGGTATTTATCCATC	2186
rs761877257	snp	A/G	1.66513e-05	0.00288537	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911989	CAGAAGAAATTAGAG[A/G]AGAGACCAGTTAATA	2186
rs761885586	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67929262	CACACGTAGTTTCTC[C/G]TCAGCAACCGAGCAC	2186
rs761891524	in-del	-/TT			intron-variant	BPTF	GRCh38.p7	17:67908493	TTGTCACTGACCACT[-/TT]TTTTTTTTTTTTTTT	2186
rs761902432	in-del	-/TT			intron-variant	BPTF	GRCh38.p7	17:67975296	GTAAGACAGTATCAC[-/TT]TGTCACAAATAAAAG	2186
rs761944198	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67914634	GACCTGGCAGTTGTG[A/G]AGGCCGACCTTTCTG	2186
rs761962881	in-del	-/AT			intron-variant	BPTF	GRCh38.p7	17:67926804	TGTAGTGGTGAGATC[-/AT]ATAGCTCATTGCAAC	2186
rs761992008	in-del	-/TAAT			intron-variant	BPTF	GRCh38.p7	17:67900575	CTCTACCAAAAATAA[-/TAAT]TAATTAATTAATTAA	2186
rs762032220	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67937833	CCTAAGATGAGATCC[A/G]GCCGGGTACAGTGGC	2186
rs762033735	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67902077	CAGCATGCTACTCTG[A/G]GATAGGTAGCATCAG	2186
rs762036633	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67839488	AATATTGATCCACCC[G/T]TACATTCCTGCAGCA	2186
rs762051522	snp	A/G	1.65652e-05	0.0028779	intron-variant	BPTF	GRCh38.p7	17:67894214	ATTGGACTCCCTTTT[A/G]AAATACTAGCCTATT	2186
rs762061890	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67977923	GCAATGGCGCGATCT[C/T]GGCTCACCACAAGCC	2186
rs762064359	snp	A/G	1.66879e-05	0.00288855	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67853955	GTAGGCGAAAACCAA[A/G]AGTACATCGGCCTCG	2186
rs762085264	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67921749	GCTTACTTAAAACAG[C/T]GGCCAGGTGCGGTGG	2186
rs762131504	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67936656	CTACCCAACCCTGCC[A/G]CCTGGCTGTGCAGTG	2186
rs762142047	snp	C/T	0.000492166	0.0156793	intron-variant	BPTF	GRCh38.p7	17:67875758	AGGTACAGAGGGCAG[C/T]GTATCAATGCCTCTG	2186
rs762144037	snp	A/G			intron-variant, utr-variant-5-prime	BPTF	GRCh38.p7	17:67889594	GGGTGGATCACTGGA[A/G]GTCAGGGGTTCAAGA	2186
rs762169503	snp	G/T	1.66618e-05	0.00288628	intron-variant	BPTF	GRCh38.p7	17:67929306	CCAATAAAGTGATAG[G/T]TTTTAATTATGGCTT	2186
rs762180260	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67868697	TATACATATAATCCT[A/G]TTAATTTTCCCCATT	2186
rs762181487	in-del	-/C			intron-variant	BPTF	GRCh38.p7	17:67915738	TCTGATCCTCATTCC[-/C]GAGCCAACTCAGATG	2186
rs762188807	snp	C/T			upstream-variant-2KB	BPTF	GRCh38.p7	17:67823585	ACAAAATATGGGCAC[C/T]TCCATTGGCCTAGGT	2186
rs762191919	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67894739	TTTTATTGACTAGAA[A/G]GAGCACTCACATTTT	2186
rs762194647	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67827819	GAATCGTTGCCAGTC[C/T]TGTCCGGGGCAGGCT	2186
rs762195415	snp	A/G			intron-variant, utr-variant-5-prime	BPTF	GRCh38.p7	17:67888810	CCCCTTCTGGAGGCC[A/G]TTCTGTTTTACCTGC	2186
rs762213825	snp	A/T			upstream-variant-2KB	BPTF	GRCh38.p7	17:67825129	AGGGAAGGGAATGAT[A/T]TTTGGGGGCTCCCTT	2186
rs762239657	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67917171	AGAGTCTCACACTGC[C/T]GCCCGAGGTGGAGTG	2186
rs762260281	snp	A/G	1.65712e-05	0.00287843	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67928573	TCAAACCTTTGCTAC[A/G]TGGGTTAAGCAAGGC	2186
rs762278880	snp	A/G	1.72758e-05	0.00293898	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67910884	TTTCACAGATGTGAA[A/G]GAGCTCTTAGATTCT	2186
rs762313294	snp	C/T	3.32978e-05	0.00408017	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67912708	CAAGGTAGAAAAAGG[C/T]GATAAGCAAACTGTG	2186
rs762355881	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67907959	CTTTTATTCTGTTAT[A/G]TAAACTTCAAGGAGT	2186
rs762366753	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67827882	AGGTATTTATGTCTT[A/G]TATGTAGAAAGGACT	2186
rs762375538	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67920250	CCTTTTAAAAAAGAC[A/G]TATTTTACAACTACC	2186
rs762435852	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67923258	AGATGGGGTTTTGCT[A/G]TGTTGTTCAGGCTGA	2186
rs762436189	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67890452	CCTGCTCATTAGTAC[A/G]AAAAGCAAAGACCCC	2186
rs762455285	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67906726	ATAGATATATTTTTT[A/G]TATCTATTTTCTCAC	2186
rs762464973	in-del	-/TG			intron-variant	BPTF	GRCh38.p7	17:67913678	TGTTTTGGAGTTCTC[-/TG]TTATTTATGTATGAA	2186
rs762476976	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67918578	AATACCAAAGTCTTA[A/C]AAAACCATATTATAA	2186
rs762486644	snp	A/G	6.66489e-05	0.00577235	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67826307	ACGGAAAGCAGCTTC[A/G]GGAGCCATAGTACCT	2186
rs762504229	in-del	-/TTTTA			frameshift-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67912189	GTAGTAAGTGGTAAT[-/TTTTA]GTTGAACCAAAGGTT	2186
rs762519914	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67905814	AAGAAAGTGATAGAG[A/G]CTTCCAAAACACTGT	2186
rs762523435	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67874190	GTTCTGTACACTGTG[G/T]TCCTTCTGTATCCCG	2186
rs762550478	snp	A/T			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67886826	AATTCATTTTTTTTT[A/T]AAGCTGCTGCATGGT	2186
rs762552906	snp	A/G	1.64844e-05	0.00287087	missense, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67886253	GAATCTGCTAAGGCA[A/G]CTGATGATCCTGAAA	2186
rs762571449	snp	A/T	0.000297031	0.0121831	intron-variant	BPTF	GRCh38.p7	17:67910854	GTAAAAATTACATTT[A/T]TATAAATGTCTTTGT	2186
rs762590101	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67856430	TCTGTTTCTTCTAAG[G/T]TGCTTTTTCCTATTC	2186
rs762595578	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67980530	ATTGCTTTTTTAAAT[A/T]GGGAAGGCCTTTGGT	2186
rs762606409	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67830795	GAGGATCAGGCTATA[A/G]CAACTGTACTTTCCC	2186
rs762609878	snp	A/G	1.64871e-05	0.00287111	intron-variant	BPTF	GRCh38.p7	17:67924598	GGCTAAGGTTAGTGA[A/G]CAGAAGAAGGCAGAG	2186
rs762618132	snp	A/T	1.76505e-05	0.00297068	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67909591	TTTTAGCCAAAAATA[A/T]TATGGATGAAAATAT	2186
rs762639948	in-del	-/TTATTC			intron-variant	BPTF	GRCh38.p7	17:67904661	GGTTTATAAGCATTG[-/TTATTC]TTATTGTTTAATCAA	2186
rs762655170	snp	A/T	8.25934e-05	0.00642572	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67928379	GAGCAGCAGAAGCCG[A/T]CAGTGATTGCAACTT	2186
rs762657223	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67844931	TATTTTTAGTAGAGA[C/G]AGCGTTTCTTCATGT	2186
rs762674762	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67884323	GTTGGCCAGGCTGCT[C/T]TCGAATGCCTGACCT	2186
rs762675628	snp	A/G			utr-variant-3-prime, downstream-variant-500B	BPTF	GRCh38.p7	17:67983276	TCCAGGACAGCAGTG[A/G]CCCCTCGTTTTATCA	2186
rs762710313	snp	C/T	1.66471e-05	0.00288501	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67912567	TCTCAGTAATGACTT[C/T]ATTGATGAAAATGGT	2186
rs762746083	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67908639	GGATCACAGTTGCAC[A/G]CCACCATGCCTGGCT	2186
rs762761701	snp	A/T	1.6686e-05	0.00288838	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67893701	TCCCTTCATCCTTTC[A/T]TCATCCCAACTGGGC	2186
rs762782270	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67928104	GGCCAGGCTGGTCTC[A/G]AACTCCTGACCTCAG	2186
rs762803594	snp	A/C	1.65436e-05	0.00287602	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67912432	CAGTACACAGACGAC[A/C]ACACCCTCAGCATCT	2186
rs762804280	snp	G/T	1.8275e-05	0.00302278	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67854762	ACCGAAGACTCATAA[G/T]GTAAGTAAATCTGGT	2186
rs762844754	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67861087	CCAAACTCATCGTTT[A/C]CCCCCATTACCTACT	2186
rs762899048	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67855401	GCTCATCCACCCTTA[A/C]CTTTGGTGTTAGGGT	2186
rs762904421	in-del	-/GAGGAGGAG			cds-indel, nc-transcript-variant	BPTF	GRCh38.p7	17:67826118	GATGACCACGAGAGC[-/GAGGAGGAG]GAGGAAGAGGAGGAC	2186
rs762912384	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67859675	CGTTTTAGCTGTTAA[A/G]ACCAATGCTTATAAC	2186
rs762923694	in-del	-/A			intron-variant	BPTF	GRCh38.p7	17:67847513	GGTGAGACTCCGTCT[-/A]AAAAAAAAAAAAAAT	2186
rs762924882	in-del	-/AATA			intron-variant	BPTF	GRCh38.p7	17:67924440	TTTTTAAATTGAGAT[-/AATA]TCATACCTTTGTATG	2186
rs762925442	snp	C/G/T			intron-variant, utr-variant-5-prime	BPTF	GRCh38.p7	17:67888933	TTTCTGACAGTAGCA[C/G/T]TCACTTGTAGATTCC	2186
rs762947170	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67882334	TTTTTGGTGGGTAGT[A/G]TTATGAAAGACATAT	2186
rs762960144	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67868873	TGTTGGGCACAAATA[G/T]ACTTTGTCTTCAGAA	2186
rs762967191	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67925679	GATATATCTATATAC[A/G]GTATTATTAACATAG	2186
rs762980892	snp	C/T			intron-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67929762	TTTCTTTATGTAAAA[C/T]AGTGGACAGCACTAG	2186
rs762983167	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67902230	AGCTTTGAGCTCCTA[G/T]GGTGTCACTGCGCTG	2186
rs762989222	in-del	-/CTC	1.65111e-05	0.0028732	cds-indel, nc-transcript-variant	BPTF	GRCh38.p7	17:67853973	TACATCGGCCTCGTT[-/CTC]CTATATTGGAAGAAA	2186
rs763018887	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67868066	GAGTATACATTCATG[A/G]ATATTTTATACTTAC	2186
rs763019764	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67959088	TCTGCCTCTTTTCTG[C/T]TTTATGCTGGTCAGA	2186
rs763023140	in-del	-/TA			intron-variant	BPTF	GRCh38.p7	17:67880948	AGGGTGTATGTATAT[-/TA]TATATATATACACAC	2186
rs763064891	snp	A/G	1.6473e-05	0.00286988	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67854313	GACGTGGCCAGAGGT[A/G]CTGCGGGTGTACTGT	2186
rs763071931	snp	A/T	1.67506e-05	0.00289396	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912188	GAGTAGTAAGTGGTA[A/T]TGTTGAACCAAAGGT	2186
rs763088429	snp	A/G	1.65102e-05	0.00287312	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67920139	AGTTCCAGAAACACC[A/G]AAAGGTAAGAAATAG	2186
rs763097831	snp	A/G	0.000133824	0.00817888	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	BPTF	GRCh38.p7	17:67893396	TAACTCTCAAGGAGA[A/G]ATTTCACGGTTGAGC	2186
rs763098967	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67975182	CATAATGATTTTCTC[C/T]TTTCTGCATATTGCC	2186
rs763109690	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67902908	GCGCTCTTAGAGACA[A/C]GAGCTCCTTTCTTTG	2186
rs763152124	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67937972	TACAAAAAATAGCCG[A/G]GCATGGTGGCGCAGC	2186
rs763161439	snp	C/T	4.94189e-05	0.00497062	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67854145	GGACTTTTGTGCAGC[C/T]CTGGTGAGCCAAGAG	2186
rs763193584	snp	A/G	2.13217e-05	0.00326503	intron-variant	BPTF	GRCh38.p7	17:67875767	GGGCAGCGTATCAAT[A/G]CCTCTGTAATGGGGG	2186
rs763199852	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67878397	GTGCATTTCTGGAGG[G/T]ACAAGCCTAGTTGTG	2186
rs763226357	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67973947	TTGTTCTGCATGCTG[A/C]CACACTTTTCATTAC	2186
rs763263667	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67826813	TAAAAGGGAATTAAG[A/G]ATTTGGACAGATTGT	2186
rs763278799	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67921925	TAGTCCCAGCTACTC[A/G]GGAGGCCGAGGCACG	2186
rs763282575	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67856026	TCAATCTGGCAATTA[C/T]GTTCTTTGATTCTGA	2186
rs763311577	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67839502	CTTACATTCCTGCAG[C/G]AAACCTCTCTTGATC	2186
rs763326289	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67877279	TTCACCTGCTTCCTT[C/T]TGTTTCTGTGGCTCT	2186
rs763352060	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67828119	GTATTTTTAGTAGAG[A/G]TGGGGTTTCACCATG	2186
rs763381003	snp	A/C/T	3.3104e-05	0.0040683	intron-variant	BPTF	GRCh38.p7	17:67929323	TTTAATTATGGCTTC[A/C/T]TCTTTTTTTAAGGCG	2186
rs763394557	snp	A/G	1.65493e-05	0.00287652	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67874898	CAGAAAAAGACAAGA[A/G]TGAGACTGAGAATGA	2186
rs763402625	in-del	-/AAAG			intron-variant	BPTF	GRCh38.p7	17:67872712	TTCTGTCTCAAAAAA[-/AAAG]AAAGAAAGAAAAAAG	2186
rs763431443	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67848847	GCTATCAGGTGGTCC[A/G]GAGTTTGCCATTCAG	2186
rs763441304	snp	C/T	0.000148311	0.00861007	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67893483	AGAAGGGAAGTATCG[C/T]GTCTACCACAATCAA	2186
rs763451277	snp	C/T	1.64866e-05	0.00287106	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67911619	GGAAAGTGACACCAT[C/T]GTTTCTTCTTCCAAG	2186
rs763461741	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67925052	TTGCACCCATCCAGG[-/T]TTTTTTTTTTTTTTT	2186
rs763513715	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67865158	AATGAGCATTTCCTT[A/T]GAACGGCATGTTGGC	2186
rs763546243	snp	A/T	9.98984e-05	0.00706677	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912702	TGTGATCAAGGTAGA[A/T]AAAGGCGATAAGCAA	2186
rs763560570	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67905045	TCTCAGATTTCCGTA[A/G]GATTGTAGAATGGAA	2186
rs763577799	snp	A/G	1.66037e-05	0.00288125	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67826217	GACGACGAGGAGGAT[A/G]AGATGGAAGAGGACG	2186
rs763577994	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67883156	TGTCTCTACTAAAAA[C/T]ACAAACAAAATTAGC	2186
rs763595062	snp	C/T	1.65427e-05	0.00287595	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67911538	TTTCATCGATGACTC[C/T]AAACTAGCCAGTGCA	2186
rs763635292	snp	C/T	1.65373e-05	0.00287548	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67866538	AACTTGCAGAATTAA[C/T]TGACTGTCTAGACAA	2186
rs763685347	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67834345	CCCAAAATTTTGTCA[C/G]TCTAAGTGAATGTTC	2186
rs763690340	snp	A/G	0.000194156	0.0098509	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	BPTF	GRCh38.p7	17:67825552	GCTGAAGGCGATCCG[A/G]AGTGGGGCCCCAGCA	2186
rs763701488	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67916327	TTGTCTTTCAGGTGG[G/T]CTCACGCCTCCCAGC	2186
rs763701544	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67933701	ATTAATAGGAGCATA[A/G]TAAGCCACAATTAAA	2186
rs763708404	snp	A/G	3.50097e-05	0.00418373	intron-variant	BPTF	GRCh38.p7	17:67903777	ATTGTCTTTCTATGC[A/G]TGAATTCTTAGGTTA	2186
rs763710098	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67841361	TTGCAGTGAGTCGAG[A/G]TTGCGCCATTGCACT	2186
rs763713791	in-del	-/A			intron-variant	BPTF	GRCh38.p7	17:67933263	GACTCCGTCTGAAGG[-/A]AAAAAAAAAAAAGGT	2186
rs763737582	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67835533	GCATTATTTGTGTAT[A/G]TGATGGTATTGCATT	2186
rs763759283	snp	G/T			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67897290	AGGTTGCGGTGAGCC[G/T]AGATCATGCCATTGC	2186
rs763782495	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67903283	TGGTCTTCGTTTTTT[A/G]GAAGGAAAAAACTCT	2186
rs763837284	in-del	-/G	2.05997e-05	0.00320927	intron-variant	BPTF	GRCh38.p7	17:67892074	AAATCTGTGGAATGT[-/G]AGATAATTTTAATTA	2186
rs763837442	snp	C/G	1.66189e-05	0.00288256	intron-variant	BPTF	GRCh38.p7	17:67932065	ATCTCAACAGCCAGT[C/G]TAGGAAATACGTAAT	2186
rs763873118	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67841051	CTTTTTTTCTTTTAC[A/G]CATCTGGGGTTCGTC	2186
rs763884235	snp	C/G	3.42648e-05	0.00413899	intron-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67918889	TAAAAGCTAAAATCA[C/G]AGGCCAGGCGTGGGC	2186
rs763890293	in-del	-/GAC	1.65726e-05	0.00287855	cds-indel, nc-transcript-variant	BPTF	GRCh38.p7	17:67874996	AAAACACCAGATGAT[-/GAC]CCTGAGCAAGGAAAA	2186
rs763897014	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67924275	CACTGTGCCCAGCTC[C/T]GACTAACTTTTGTAT	2186
rs763939294	snp	C/T	0.000314083	0.0125277	intron-variant	BPTF	GRCh38.p7	17:67920152	CCAAAAGGTAAGAAA[C/T]AGAATTCTATTCTTT	2186
rs763954213	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67891348	GTTTTATATTGATAA[A/G]CCTACACAGATAATT	2186
rs763959358	snp	A/C	1.68303e-05	0.00290084	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912208	GAACCAAAGGTTAAT[A/C]ATATAAATAAAATAA	2186
rs763965110	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67842544	CCAGATAAACTCCAC[A/G]TTGTAGGAAATAAAA	2186
rs763992744	snp	A/G	1.65974e-05	0.0028807	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67922844	CCTTTCCAAAGAAAC[A/G]CCTACACCTCAGAGG	2186
rs763996379	snp	C/G			utr-variant-3-prime, downstream-variant-500B	BPTF	GRCh38.p7	17:67983307	TTCCCAGTCCATTGT[C/G]ATCACGTCAGAGAAA	2186
rs764003531	snp	A/G	4.98965e-05	0.00499457	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912329	AAAGAAACAGCTCCG[A/G]AACAAAATCGCATTT	2186
rs764015064	snp	A/G	1.64727e-05	0.00286986	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67854175	GCAGTGCACACTCAT[A/G]GCAGAGATGCATGTT	2186
rs764029218	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67939074	ATTGGAATAACCTTT[C/G]AAAACTTCAACTTAG	2186
rs764056721	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67858378	AACACGGAAACCTTT[A/G]TCAGCAAGGTCATTC	2186
rs764062575	snp	A/G	1.66768e-05	0.00288758	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67893693	AAACAACATCCCTTC[A/G]TCCTTTCTTCATCCC	2186
rs764068213	snp	A/G	1.6473e-05	0.00286988	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67854322	AGAGGTGCTGCGGGT[A/G]TACTGTGAGAGTGAT	2186
rs764074886	in-del	-/ATATAC			intron-variant	BPTF	GRCh38.p7	17:67880955	ATGTATATTATATAT[-/ATATAC]ACACACACACACACA	2186
rs764080472	snp	C/T			intron-variant, missense	BPTF	GRCh38.p7	17:67929043	ATCCAGTCACTATGG[C/T]AGGAAAAGTAATTAC	2186
rs764130268	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67831037	TCTTTCACATCTGTT[C/T]AATTTTGGGTATTGG	2186
rs764167122	in-del	-/ACT	0.000216189	0.0103946	cds-indel, nc-transcript-variant	BPTF	GRCh38.p7	17:67912769	ACTGTCACAACCACC[-/ACT]ACAACAGTGACCAAG	2186
rs764169411	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67949723	TATATATATAATTTA[C/T]ACATAATTACACAGC	2186
rs764173542	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67851795	GGTGTTTCCATTGTT[C/T]TGCATCCTTCCCAAC	2186
rs764189207	in-del	-/TAAATCTCAAAGAGGT			intron-variant	BPTF	GRCh38.p7	17:67859488	TATAGATAAAGAGAC[-/TAAATCTCAAAGAGGT]TAAATAATTTGCCCT	2186
rs764224641	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67935490	GTAATAATAATTACA[A/G]AACAGAAAAGACCAA	2186
rs764248961	snp	C/T			missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912788	CAACAGTGACCAAGC[C/T]TTCCACACCCTCCAC	2186
rs764253883	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67845511	GGCATGGTGGTTCAC[A/G]CTTGTAATCCTAGCA	2186
rs764272237	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67900405	CCACCGCGTTCAGCC[A/T]AATGTAACAAGAAAT	2186
rs764303775	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67874671	TGTTTGTAATCTTGA[-/T]TTTTTATTTCATAGG	2186
rs764326248	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67910677	TGGTGGCACATGCCT[A/G]TAATCCCAGCTACTT	2186
rs764327112	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67898824	CACTTTGGGCAACCA[C/T]GTCAGGAGAATCACT	2186
rs764327671	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67865631	AAAATCAGGCTCACT[C/G]TCATCGAGTGCCTCA	2186
rs764331098	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67913343	GATACAGAAAGCTTC[A/C]AAATTGGCCAACTAA	2186
rs764381304	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67947110	TCTCTTTCCAGCCAC[A/T]TGAGATTATTGCAAT	2186
rs764415539	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67866879	CATAGAGTACACTTA[C/G]ACAAACCATACACCT	2186
rs764425294	snp	C/T	1.71625e-05	0.00292933	intron-variant	BPTF	GRCh38.p7	17:67853934	ATGTCACGTCTTTAT[C/T]TACAGGTAGGCGAAA	2186
rs764445196	snp	A/G	2.21285e-05	0.00332623	intron-variant	BPTF	GRCh38.p7	17:67854795	TAATTTTTTGTATGC[A/G]TTTAAAATTAGACTA	2186
rs764527892	snp	A/G	3.37115e-05	0.00410543	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67909636	AAAGAAAATGTTCAC[A/G]AAGTCCAAAAAAAAT	2186
rs764561355	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67853186	TTATTTATATTGATA[C/T]ATTTATATACTTACA	2186
rs764562591	snp	A/G	1.70551e-05	0.00292015	intron-variant	BPTF	GRCh38.p7	17:67909780	AGGAGAGTCAGCTGT[A/G]GAGGGCAGCCTGGGG	2186
rs764577445	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67936615	GAGTCTTGAATCCCC[C/T]GTGAGGATAGGGTTT	2186
rs764579304	snp	C/T	1.69991e-05	0.00291535	missense, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67891859	TAGGTGATTTCAAAT[C/T]GGAGAAGTCCAACGG	2186
rs764606782	in-del	-/T	4.08384e-05	0.00451858	intron-variant	BPTF	GRCh38.p7	17:67893351	ATAAATAATGCAGTC[-/T]TTTTATTTTTTTGGT	2186
rs764612522	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67860435	TATTGCTTTTATTTA[A/T]TAAGTGCTTAAAAAT	2186
rs764625598	snp	C/T	3.33289e-05	0.00408207	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67912621	TGTCAATGGAGAATC[C/T]AAAAGAAAAACCGTC	2186
rs764660705	in-del	-/TTCTT			intron-variant	BPTF	GRCh38.p7	17:67863278	TGCCTCTATGCTACC[-/TTCTT]TTCTTTTTCTTTTCA	2186
rs764682478	snp	A/G	3.39553e-05	0.00412025	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67903808	CACCGGATGACATCA[A/G]TTGAAAGAGAAGAAA	2186
rs764701129	snp	C/G	1.65124e-05	0.00287331	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67928559	AACAAGAACTTTCAT[C/G]AAACCTTTGCTACAT	2186
rs764721025	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67934339	CCTGGCCAACATGGT[A/G]AAACCCCTTCTCTAC	2186
rs764733639	snp	C/G	1.65111e-05	0.0028732	intron-variant	BPTF	GRCh38.p7	17:67903947	CAACCCTTTAAAATA[C/G]TGTTAGCCATTTCTG	2186
rs764758708	snp	C/G/T	3.2973e-05	0.00406025	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911618	AGGAAAGTGACACCA[C/G/T]TGTTTCTTCTTCCAA	2186
rs764760963	snp	A/G	1.66015e-05	0.00288105	missense, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67891982	AGCTGAAGAGCCAGC[A/G]GGTGGCAGCCGCTGC	2186
rs764846463	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67905658	AGGCTGCAGTAAGCT[A/G]TAATTGTGCTGTTGC	2186
rs764855294	in-del	-/TTTGT			intron-variant	BPTF	GRCh38.p7	17:67865734	ACATTAATTTGCCTG[-/TTTGT]TTTAAGTTAGTGACC	2186
rs764877810	snp	C/G	3.33095e-05	0.00408089	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67826210	TTCTGAGGACGACGA[C/G]GAGGATGAGATGGAA	2186
rs764881405	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67901611	CAAGACAAAGGATTT[A/G]AATAGGCATTTTGCA	2186
rs764889053	in-del	-/TTTGT			intron-variant	BPTF	GRCh38.p7	17:67883588	CTTGAATGTTGCTTG[-/TTTGT]TTTGTTTTGTTTGTG	2186
rs764907836	in-del	-/AA			intron-variant	BPTF	GRCh38.p7	17:67870002	GCGAGACTCCGTCTC[-/AA]AAAAAAAAAAAAAAA	2186
rs764915029	snp	A/C	1.64754e-05	0.00287009	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67854347	AGTGATAAGGAGTAC[A/C]ATCACGTTCTTCCTT	2186
rs764925244	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67844887	GAGCTGGGATTATAG[A/G]CATGTGCCACCACGC	2186
rs764969747	snp	A/C/T	3.31325e-05	0.00407005	intron-variant	BPTF	GRCh38.p7	17:67920168	AGAATTCTATTCTTT[A/C/T]ATGATTAACCTGTTA	2186
rs764976740	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67859987	TCAAATATTTTATTT[C/T]TCTTAGTGGAACAGT	2186
rs764992740	snp	G/T	1.64817e-05	0.00287064	synonymous-codon, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67886243	TTCCCAGAGTGAATC[G/T]GCTAAGGCAGCTGAT	2186
rs765006682	in-del	-/AG			intron-variant	BPTF	GRCh38.p7	17:67904052	TATTTATTTTGAGAC[-/AG]AGTCTCGCTCTGTTG	2186
rs765039954	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67855811	ATCTGGTAGGATGAA[A/G]TGAATGTCAGAGCAG	2186
rs765073832	snp	A/G	1.65649e-05	0.00287788	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67912366	TTCTTCAGATGCTGA[A/G]GGTAACTACCGAGAT	2186
rs765081712	snp	A/C	1.66029e-05	0.00288117	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911131	CGACTCGAAAAAATC[A/C]AGTTGGAGGGTGGAA	2186
rs765084388	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67892738	TAGCAGCCCAGTACA[C/T]ATATTCAAAAGCTTT	2186
rs765095543	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67879968	ATTTTTGGCAGGACA[A/G]ACATCTAAACTATCC	2186
rs765097004	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67844151	GTGGCATGATCTCAG[C/T]TCACTGCAACCTCCG	2186
rs765110277	snp	A/G	1.64727e-05	0.00286986	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67854518	TGTAGGGTTTGTCAC[A/G]AACTTGGGGATTTGC	2186
rs765112656	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67952781	AAATCCCTAATGTAA[C/T]GTATTCATCATCACA	2186
rs765122629	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67842924	AAGGTCTTTAGGCCA[A/G]AGGAAATACTAGAAC	2186
rs765139186	snp	A/G	1.65427e-05	0.00287595	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67912423	AGAGTCTGACAGTAC[A/G]CAGACGACCACACCC	2186
rs765160727	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67914677	TAAAATGGAGGGTAG[A/G]CTCAACTGGGAAGCA	2186
rs765165970	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67978475	AGCTGATTTTTGTAT[C/T]TTTAGTAGAGACGGG	2186
rs765178080	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67926108	AATCTCCTGGGCTCA[A/G]GCAATCTACCCACCT	2186
rs765204076	snp	A/C/G	6.76903e-05	0.00581732	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67913149	TTTGGATATATGGCC[A/C/G]TATCCTTCTCCTAGA	2186
rs765209552	snp	A/G	1.79213e-05	0.00299338	intron-variant	BPTF	GRCh38.p7	17:67875537	TATCTTTGAAGTTTT[A/G]TTGTGCATTTTGCTG	2186
rs765226731	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67862247	CCGAAAGTGCTGGGA[-/T]TTACAGGCGTGAGCC	2186
rs765228070	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67895603	GAGTAGTTGGGACTA[C/T]AGACGCATTCCACTA	2186
rs765261129	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67852451	TACCTTATCACTATC[C/T]CCTTGCCCTCCTTTT	2186
rs765262200	snp	A/G	3.29875e-05	0.00406112	intron-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67918843	TACACGGACAGGTAA[A/G]GGGGAAGGGAGTTAT	2186
rs765262835	snp	A/G	1.65701e-05	0.00287833	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67853964	AACCAAGAGTACATC[A/G]GCCTCGTTCTCCTAT	2186
rs765264365	snp	A/G	1.65004e-05	0.00287227	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67911874	TGTTGAAGTCTTGGA[A/G]CCGTTAAAGTGTGAG	2186
rs765268110	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67955246	TAGCGCCACTGCACT[C/T]CAGCCTGGGCGACAG	2186
rs765292059	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67900747	GCACACAGTAGCTCA[C/T]GCCTGTAATCCCAAC	2186
rs765326858	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67924841	AGCTCACCGAGCCTC[A/G]ACATCCCTGGTTCAA	2186
rs765334548	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67936669	CCGCCTGGCTGTGCA[A/G]TGCTCATTTAATGTA	2186
rs765387659	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67920603	AATGTTTATAGAGCA[C/T]CAGTACAATAGGCAC	2186
rs765397573	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67902189	TTGCCTCATGGACAC[C/G]AAGAACACAACTGAG	2186
rs765404287	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67867970	TATGTTCTACCTTCT[C/T]GAAGGGGCAATATCT	2186
rs765412513	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67830539	CATTTTAAGGAGGGC[A/G]AGATAATATACCCCA	2186
rs765413735	snp	C/T			intron-variant, utr-variant-5-prime	BPTF	GRCh38.p7	17:67888819	GAGGCCATTCTGTTT[C/T]ACCTGCCTAGTTCCT	2186
rs765443034	snp	C/T	1.64732e-05	0.0028699	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67854122	AGATTATCTCCTTTT[C/T]GCTTTGAGGACTTTT	2186
rs765459740	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67852303	TTAAAATTTTATAAC[A/G]AAAATACATGTATGA	2186
rs765497108	snp	A/G	5.17166e-05	0.00508484	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67910885	TTCACAGATGTGAAG[A/G]AGCTCTTAGATTCTG	2186
rs765501394	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67838660	TTTTTATATTTTTTT[A/G]GTAGAGACGAGGTTT	2186
rs765517394	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67946958	CCTATAGCTTGCTTC[G/T]CTCAGCACTAGGCAG	2186
rs765543559	snp	G/T	1.6477e-05	0.00287024	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67928448	TCTCCAGCACAGAAG[G/T]TTATGGTGGCCCCCA	2186
rs765545706	snp	A/G			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67896367	TCTCGTAAGTTTACA[A/G]TAGAAGGAAAACATT	2186
rs765553989	snp	C/T	1.68852e-05	0.00290557	missense, utr-variant-5-prime, nc-transcript-variant	BPTF	GRCh38.p7	17:67893386	TACTGGTAGTTAACT[C/T]TCAAGGAGAAATTTC	2186
rs765554080	snp	C/T			upstream-variant-2KB	BPTF	GRCh38.p7	17:67823646	TACTTACCTGGTCCC[C/T]GGAGACATATACACA	2186
rs765572681	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67973235	AAAAATTAGCAAGGC[A/G]TGGTGGCAGATGCCT	2186
rs765602921	snp	C/T	5.03537e-05	0.0050174	missense, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67891997	AGGTGGCAGCCGCTG[C/T]ACATGAAGCAAATAA	2186
rs765631305	snp	A/G	6.64463e-05	0.00576357	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67928577	ACCTTTGCTACATGG[A/G]TTAAGCAAGGCCAGT	2186
rs765647116	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67875759	GGTACAGAGGGCAGC[A/G]TATCAATGCCTCTGT	2186
rs765650702	snp	A/G	6.6599e-05	0.00577019	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912709	AAGGTAGAAAAAGGC[A/G]ATAAGCAAACTGTGG	2186
rs765705928	snp	C/T	1.65345e-05	0.00287524	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911546	ATGACTCTAAACTAG[C/T]CAGTGCAGATGATAT	2186
rs765715313	snp	C/T	1.64904e-05	0.00287139	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67866576	TGGGAAGCAGAACTC[C/T]GCAAAATTCTAGAAG	2186
rs765720157	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67869363	AAAGTCAAAACAGGA[A/C]TGGGTAATCAAGTGT	2186
rs765725443	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67839496	TCCACCCTTACATTC[C/G]TGCAGCAAACCTCTC	2186
rs765727766	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67846533	GGTCTCATACTTTAT[A/T]ACATTGTCACTTCAC	2186
rs765745975	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67942828	AGATGATTCTCACAA[A/G]TATATAATGGTAAGC	2186
rs765757473	snp	C/T			utr-variant-3-prime	BPTF	GRCh38.p7	17:67984172	TTCTGCATCTCATCA[C/T]GTCACAGTATTTCTG	2186
rs765770406	snp	A/G	3.29625e-05	0.00405958	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67866664	CTCGGGGCAGTAACA[A/G]ATCCTTTCTGGCGGC	2186
rs765772336	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67885344	TCCCAGCCACTTTGG[A/G]AGGCCAAGGTGGGTG	2186
rs765780995	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67861838	CTGTTGGCTAACTAG[C/T]TCATTCTTGAGGTCT	2186
rs765813820	snp	A/C	1.65614e-05	0.00287757	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912843	TGTAAAGGAGCAGAG[A/C]AAAACCGTGGTCACC	2186
rs765850453	snp	C/T	1.64787e-05	0.00287038	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67922927	AAACTGGCCCTGTTA[C/T]TATTGAAACCTGGGT	2186
rs765864376	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67964077	GAACTGGAATGTCAA[C/T]CTTGAAAGTATTAAA	2186
rs765872191	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67908047	AGGATCATAGCATTT[A/T]TCCATTTCTAATAGG	2186
rs765896952	snp	C/T	1.6486e-05	0.00287102	missense, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67886254	AATCTGCTAAGGCAG[C/T]TGATGATCCTGAAAA	2186
rs765900222	snp	C/T			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67898252	CTTTAGTCCCAGCTA[C/T]TAGGAGGCTGAGGCA	2186
rs765938230	snp	C/G	1.64904e-05	0.00287139	intron-variant	BPTF	GRCh38.p7	17:67924609	GTGAACAGAAGAAGG[C/G]AGAGGACATCAAGGC	2186
rs765974479	in-del	-/T			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67888031	TGCCTCCAGCAAAAG[-/T]TGGGTAGGAATGGTT	2186
rs765986942	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67894840	CAACCAAAGATCATA[C/T]AGCTCCTGAGTAGAC	2186
rs765989620	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67862952	CACCTAACAGTTCTT[C/T]AGCCTCTTCCCATTA	2186
rs765991651	snp	A/C	1.65627e-05	0.00287769	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912455	CAGCATCTTGTCCAG[A/C]AAGCAATTCAGTTAA	2186
rs765998197	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67844955	TTCATGTTGGTCAGG[C/G]TGGTCACGAACTTCC	2186
rs766041853	snp	A/G	1.65581e-05	0.00287728	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912374	ATGCTGAAGGTAACT[A/G]CCGAGATAGCCTTGA	2186
rs766078633	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67906754	CACACCAGTATCTTG[C/T]TCGCGACAGAATTAT	2186
rs766118783	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67845927	GCCATACTTACTTGG[A/G]GAAAAAACTAAAGAG	2186
rs766131511	in-del	-/TTTTTTTTTT			intron-variant	BPTF	GRCh38.p7	17:67843757	CTGGAGCAGTTGTCT[-/TTTTTTTTTT]TTTTTTTTTTTTTTT	2186
rs766147447	snp	A/G			intron-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67929787	CACTAGACCACCCAC[A/G]GAAGTGTGCTGTGCA	2186
rs766150640	snp	A/G	1.84988e-05	0.00304123	intron-variant	BPTF	GRCh38.p7	17:67854765	GAAGACTCATAATGT[A/G]AGTAAATCTGGTCTT	2186
rs766217452	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67913272	ATTTTTAAAAAATGA[G/T]ATAATAGAGATAAGA	2186
rs766222492	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67880998	ATATATATTACATAT[A/C]TATATTTCAGGCTTT	2186
rs766224076	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67830812	AACTGTACTTTCCCC[A/C]TTTTCTGTAGAATAG	2186
rs766229534	snp	A/G	3.33339e-05	0.00408238	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911255	CGATGAGACAAGAAC[A/G]GAGCCCAAATGCAAA	2186
rs766235349	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67868074	ATTCATGGATATTTT[A/C]TACTTACTGGGTTAT	2186
rs766238810	in-del	-/A			intron-variant	BPTF	GRCh38.p7	17:67871441	TGAGACTTTGTCTCC[-/A]AAAAAAAAAAAAAAA	2186
rs766263856	in-del	-/GAGGAG	0.187574	0.24208	cds-indel, nc-transcript-variant	BPTF	GRCh38.p7	17:67826118	GATGACCACGAGAGC[-/GAGGAG]GAGGAGGAAGAGGAG	2186
rs766283059	snp	C/G	1.66988e-05	0.00288949	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67893703	CCTTCATCCTTTCTT[C/G]ATCCCAACTGGGCAT	2186
rs766336562	snp	A/C	3.29582e-05	0.00405931	missense	BPTF	GRCh38.p7	17:67931944	ATTCGCCCTGGTATG[A/C]CCGTGATTAGAACAC	2186
rs766398164	snp	A/G	3.46662e-05	0.00416316	intron-variant	BPTF	GRCh38.p7	17:67909795	GGAGGGCAGCCTGGG[A/G]GTGATAAGAATGCAC	2186
rs766405801	snp	G/T	1.65403e-05	0.00287574	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67874973	CCCTTGAAAAAGACA[G/T]TGACGACAAAACACC	2186
rs766450254	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67915146	TATTAATGTTAAGGC[A/T]GAGCAATATTGGAAA	2186
rs766468694	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67875834	CTAAAACCTTAAACT[A/G]TGTGTTCATTCATGC	2186
rs766473674	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67877357	TGCCTGGCTATGTGC[C/T]AGACACTTTGTGATG	2186
rs766482363	snp	C/T	4.94189e-05	0.00497062	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67894097	TGCATTGGCTTTAGC[C/T]ATTTTGGAGTGTGCA	2186
rs766516633	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67855413	TTAACTTTGGTGTTA[A/G]GGTTGTTTTACTTCT	2186
rs766519637	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67895431	GCTAAAGGTATGGCT[C/T]CCAGTTTTCTTTGGT	2186
rs766521873	snp	A/G			intron-variant, utr-variant-5-prime	BPTF	GRCh38.p7	17:67889794	GCCTGGGCGACAAGA[A/G]CGAAACTCCATCTCA	2186
rs766544864	snp	A/G			intron-variant, utr-variant-5-prime	BPTF	GRCh38.p7	17:67889023	ACCCTCCACTTCCTC[A/G]GTTTATCTGTTTAGT	2186
rs766548171	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67938785	AAAATTGCAAGTTTA[A/G]AAATAAAAACGTAGA	2186
rs766549626	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67839569	ATTTTAATTTTTAAA[C/T]AGTTTATACATGTAC	2186
rs766550252	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67922097	GATGGGCAGAGACAC[A/C]GATGGGAGATGTACC	2186
rs766609106	in-del	-/AAC			intron-variant	BPTF	GRCh38.p7	17:67939200	CCATGGCGTTAGTTT[-/AAC]AACAACAACAAAAAG	2186
rs766620288	snp	A/G	4.94368e-05	0.00497152	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67893484	GAAGGGAAGTATCGC[A/G]TCTACCACAATCAAT	2186
rs766633046	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67876088	TGATCTGACCTTTCC[A/T]GTTCTGTAGATACTA	2186
rs766638745	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67868072	ACATTCATGGATATT[G/T]TATACTTACTGGGTT	2186
rs766641672	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67840645	GAGCCCGTCATTCCC[C/T]GCCTACCCAAGGCTC	2186
rs766667187	snp	C/G	1.64852e-05	0.00287094	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911624	GTGACACCATTGTTT[C/G]TTCTTCCAAGAGTGC	2186
rs766681804	snp	C/T	3.33567e-05	0.00408378	missense, utr-variant-5-prime, nc-transcript-variant	BPTF	GRCh38.p7	17:67893403	CAAGGAGAAATTTCA[C/T]GGTTGAGCACCAAAA	2186
rs766698348	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67909887	AAAACATAATTGATA[A/T]CCCATACAATTCACC	2186
rs766706813	snp	A/G	1.70589e-05	0.00292047	intron-variant	BPTF	GRCh38.p7	17:67928609	AAATTCAGGTATGGA[A/G]CTATCATTAAGTAAA	2186
rs766745154	snp	A/G	1.64923e-05	0.00287156	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67866677	CAAATCCTTTCTGGC[A/G]GCAGCTAATGGTGAG	2186
rs766763161	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67898555	CCTCAAGTTATCCTC[C/T]CACCTTGACCTCCCA	2186
rs766774926	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67863517	TCTCCATCTCCTGAC[C/G]TTGTGATCTGCCCGC	2186
rs766814529	snp	A/G	3.31016e-05	0.00406813	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67912861	AACCGTGGTCACCAC[A/G]ACAGTGACAGACTCC	2186
rs766849586	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67834562	GTTCTAGCAATCTTC[A/G]TGTATTTTGAGGCTT	2186
rs766863809	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67932298	CCGTATAGCAAAAGA[C/T]AGAAAATCAAGGAGA	2186
rs766864441	snp	A/G	1.65168e-05	0.00287369	intron-variant	BPTF	GRCh38.p7	17:67903956	AAAATAGTGTTAGCC[A/G]TTTCTGAGACTTTTA	2186
rs766883695	snp	C/G	9.11918e-05	0.00675186	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67826168	GGAGGAGGAGGAGGA[C/G]GACGGCGACGCCGAG	2186
rs766891955	in-del	-/G			intron-variant	BPTF	GRCh38.p7	17:67968166	CTAAAACCTTCCAAA[-/G]GATCACTTACCACTA	2186
rs766944913	snp	A/C			intron-variant, synonymous-codon	BPTF	GRCh38.p7	17:67946052	GGTTCTCTCTCAGAT[A/C]CAGTCACAGGTTGTG	2186
rs766947858	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67869972	GCCACTGCACTCCAG[C/T]CTGGGCGACACAGAG	2186
rs766956946	snp	C/T			utr-variant-3-prime	BPTF	GRCh38.p7	17:67983860	TTCTTAAAAGAAAGA[C/T]GTTGCTACAGTTCCC	2186
rs766978419	snp	C/T	1.64819e-05	0.00287066	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67911730	AAAACTGGGATGTGA[C/T]TCTGAATCTAATAGC	2186
rs767002314	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67942340	AAAAAAAAAGGACAA[A/G]CCAACATTATGAGGA	2186
rs767023939	snp	A/G/T	3.31231e-05	0.00406948	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67866528	ACAAAGGTCCAACTT[A/G/T]CAGAATTAATTGACT	2186
rs767024419	snp	A/G	6.66467e-05	0.00577225	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912611	AAAATGAAAATGTCA[A/G]TGGAGAATCTAAAAG	2186
rs767088881	snp	A/G	6.09267e-05	0.00551903	intron-variant	BPTF	GRCh38.p7	17:67854782	GTAAATCTGGTCTTA[A/G]TTTTTTGTATGCATT	2186
rs767091070	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67881355	CTGGTTAATTGATAT[C/T]GTATCCCATCAAAAG	2186
rs767101396	snp	A/T	1.64784e-05	0.00287035	synonymous-codon	BPTF	GRCh38.p7	17:67931952	TGGTATGACCGTGAT[A/T]AGAACACCACTCCAA	2186
rs767123862	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67884547	CAGCCCCTCAAGTAC[A/G]TAGGACTAGAGGCAT	2186
rs767140242	snp	C/G	1.65523e-05	0.00287678	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911405	ATGTCTCCATTCGGA[C/G]CCCAGAAACAAAATG	2186
rs767162214	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67886501	ATTTTTTTTTTAAAC[A/T]CAGCACTTGCACTCA	2186
rs767169582	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67932104	TTTGGCACTACATAC[A/G]AGAAATATAATTTTA	2186
rs767192862	in-del	-/CTC	2.48062e-05	0.00352172	cds-indel, nc-transcript-variant	BPTF	GRCh38.p7	17:67826147	AGAGGAGGACATGGT[-/CTC]CGAGGAGGAGGAGGA	2186
rs767204968	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67907849	AATAATCTGATTCTC[A/C]GTCCATATTCCACTT	2186
rs767215698	snp	C/T			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67896624	ACAATGTTACAGTAT[C/T]GTTTAGGGATATAGA	2186
rs767272679	snp	C/T	1.6654e-05	0.00288561	intron-variant	BPTF	GRCh38.p7	17:67932053	TTATCATTTTACATC[C/T]CAACAGCCAGTCTAG	2186
rs767351237	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67869246	ATAGGATTTTATAAA[A/G]TACATTGAATTAAAA	2186
rs767356004	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67902396	TGGCATAGTCACCCC[A/G]CCTTACTCCTGTAGC	2186
rs767362095	in-del	-/T	3.59955e-05	0.00424222	intron-variant	BPTF	GRCh38.p7	17:67874789	TATATATAGGAATAA[-/T]TTTTTTTGTTTGTTT	2186
rs767374997	snp	A/T	1.81243e-05	0.00301029	intron-variant	BPTF	GRCh38.p7	17:67903748	ATCTTTTCTGTTTAT[A/T]TTTCCAAGTTAACAT	2186
rs767384115	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67856402	CAGGTTTTTTTCTCT[A/C]CTCTGTGCATGGTCT	2186
rs767396953	snp	C/G	3.29495e-05	0.00405877	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67894127	AGTTAAACCAGTTGT[C/G]ATGCTACCAATATGG	2186
rs767397995	snp	C/T	3.3036e-05	0.0040641	splice-donor-variant	BPTF	GRCh38.p7	17:67920145	AGAAACACCAAAAGG[C/T]AAGAAATAGAATTCT	2186
rs767406798	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67838144	CTCAGCTCTGCCCTC[A/T]TAGCAGGAAAGCAGC	2186
rs767455219	in-del	-/TT			intron-variant	BPTF	GRCh38.p7	17:67840106	TGGAAAAATACTGAT[-/TT]TTTTTTTTTTTTTTG	2186
rs767469367	snp	C/T	4.97682e-05	0.00498815	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67911121	AGAAAAACAGCGACT[C/T]GAAAAAATCAAGTTG	2186
rs767477733	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67846072	TCTTGAATATAGGGT[A/G]ACATTCACTAGTGGT	2186
rs767479098	snp	C/T	1.65919e-05	0.00288022	intron-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67918856	AAGGGGGAAGGGAGT[C/T]ATTTTCTAATTTAAG	2186
rs767495681	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67938960	TAGCACTGTGATACA[C/T]GATACTATTTGCAGT	2186
rs767496985	snp	C/T	1.65847e-05	0.0028796	synonymous-codon, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67875659	CTCTGAAGGGAGGAG[C/T]CCTGTGGGGTGTCTC	2186
rs767506733	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67836294	GGAAACGGCATGGCC[A/G]TGTGATTCATACCAA	2186
rs767525391	in-del	-/CTTTAAAG			intron-variant	BPTF	GRCh38.p7	17:67900608	AAAAAGCTAAGCAAT[-/CTTTAAAG]CTTAACTAAAGACAT	2186
rs767541147	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67975365	TCTAATACCAGGATC[A/G]TAAAGCCACTAGTAC	2186
rs767560058	snp	A/G	8.28645e-05	0.00643625	missense, utr-variant-5-prime, nc-transcript-variant	BPTF	GRCh38.p7	17:67893416	CACGGTTGAGCACCA[A/G]AAAGGAAGTGATCAT	2186
rs767571645	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67829414	TGCATAGGTATACGT[G/T]TGCCATGGTGGCTTG	2186
rs767578126	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67949839	GAGGCAGGTGGATCA[C/T]CTGAGGTCAGTTCAA	2186
rs767585033	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67903156	ATGGGCCCCTTTCTC[C/T]GCGGATGTAAGAAAC	2186
rs767587923	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67865503	TAGAGACTCAGAGAG[A/G]CTGTGTCTTGTCCAT	2186
rs767641561	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67923943	ACCTCCCAGATTCAA[A/G]CAATTCTCCTGCCTC	2186
rs767694893	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67925619	AAAATACTGTAAGAG[G/T]TTTTACCAACTTCAG	2186
rs767697673	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67877589	AAGATAACTGTCAGA[C/T]TGGAAAGCATTTTGG	2186
rs767737434	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67913655	AGCTTAGTTGCATGA[A/T]AAACATTTGTTTTGG	2186
rs767759631	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67964892	TAGTCCTAGCTACTC[A/C]GGAGGTTGAGGCAGG	2186
rs767763183	snp	C/G	0.00013274	0.00814571	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67929462	CCAATACCTCAGGCT[C/G]TGGAGGAACCACAAG	2186
rs767767053	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67891041	ACAAAAAATTAGTCA[C/G]GTGTGCTGGTGCATG	2186
rs767770726	in-del	-/AA			intron-variant	BPTF	GRCh38.p7	17:67934026	TCCAACGTGGGCAAC[-/AA]GAGTGAAACTCCATC	2186
rs767781715	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67863579	GTGAGCCACCACGCC[C/T]GGCCCATTACCTTCT	2186
rs767818477	snp	A/G	1.65203e-05	0.002874	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67913038	CAAGAGCAGCAAGAA[A/G]AGCATTTTTGTTTTG	2186
rs767858872	snp	A/G	1.65381e-05	0.00287555	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67874934	AAGATGCTGAGAAAA[A/G]CAGAGAAGAATTTGA	2186
rs767907652	in-del	-/TTTTT			intron-variant	BPTF	GRCh38.p7	17:67881492	TTTCCATAATCAAGG[-/TTTTT]TTTTTTTTTTTTTTT	2186
rs767910804	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67851702	GCTGTTCAGTTATAA[A/G]CAGAACCTTAAACTT	2186
rs767914903	snp	A/C/T	3.30919e-05	0.00406756	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67826254	ACTCCGATTATCCGG[A/C/T]GGAGATGGAAGACGA	2186
rs767923628	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67918640	AGCCCTTCAGTTTAG[C/T]AGAGTGAATATGAAT	2186
rs767943276	snp	C/T	1.648e-05	0.0028705	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67911757	TAGCACTTTGGAAAA[C/T]AGTTCTGATACCGTG	2186
rs767956321	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67866084	CACGATGGTGCCACT[A/G]CACTCTAGCCCGGGC	2186
rs767959144	in-del	-/G			intron-variant, utr-variant-5-prime	BPTF	GRCh38.p7	17:67888803	GAAGATTCCCCTTCT[-/G]GAGGCCATTCTGTTT	2186
rs767976890	snp	A/G	1.64996e-05	0.0028722	synonymous-codon, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67886276	TCCTGAAAATGGAGA[A/G]AGAGAATCTCATACA	2186
rs767982014	in-del	-/AG			intron-variant	BPTF	GRCh38.p7	17:67900533	CAGGAGTTCAAGACC[-/AG]AGCCTGGGCAACATA	2186
rs767994526	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67898597	TTACAGGTGTGAGCC[A/G]CTGCACTTGGCCTAT	2186
rs768001370	snp	C/T	3.34454e-05	0.0040892	intron-variant	BPTF	GRCh38.p7	17:67929292	CCACGTAATGCTTTC[C/T]AATAAAGTGATAGTT	2186
rs768006052	in-del	-/CT	1.6752e-05	0.00289408	frameshift-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67912190	TAGTAAGTGGTAATG[-/CT]TTGAACCAAAGGTTA	2186
rs768017094	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67938795	GTTTAGAAATAAAAA[C/T]GTAGATGGCAAAGTG	2186
rs768023890	snp	A/G	1.65002e-05	0.00287225	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911014	GTCAATGTTAGTGAG[A/G]GTTTTCATCTAAGGA	2186
rs768029546	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67917539	TTGTTCATGTTTTGA[A/G]TAACCACCATTTGGA	2186
rs768059042	in-del	-/A	0.00585565	0.0537916	frameshift-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67903835	GAAAAGGAGAAAGTC[-/A]AAAAAAAAGAGAAGA	2186
rs768065176	snp	A/C	1.64963e-05	0.00287192	intron-variant	BPTF	GRCh38.p7	17:67924627	AGGACATCAAGGCCC[A/C]AATGGAGGCTCTTTC	2186
rs768100329	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67935350	GAGGATCACATGGGC[C/T]CAAGAGGTCAAGGCT	2186
rs768123811	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67851165	GCAGAGTCTGGGACC[C/T]TAGCTCTTTTTGTAA	2186
rs768152790	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67885556	GATTGTGCCACTGCA[C/G]TCCAGCCTGCGCAAC	2186
rs768157442	snp	G/T	0.000149292	0.0086385	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912815	CCACAGGCGGCAGTG[G/T]GGACATCATCTCTGT	2186
rs768194749	snp	A/G	6.75459e-05	0.00581106	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67909628	GTCAGATAAAAGAAA[A/G]TGTTCACGAAGTCCA	2186
rs768285922	in-del	-/A			intron-variant	BPTF	GRCh38.p7	17:67916765	GCAATACTCTGTCTC[-/A]AAAAAAAAAAAAAAA	2186
rs768306758	snp	C/T	1.65031e-05	0.00287251	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67893453	AAATATCAACAATTA[C/T]TTTAAATTGGGTCAA	2186
rs768345781	snp	A/G			missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911158	GGAATTAAGGGTATA[A/G]GAAAGACTTCTACAA	2186
rs768365676	snp	A/G	4.957e-05	0.00497821	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912920	CATCTATGACTGTGA[A/G]CAAAGAGTATTCCAC	2186
rs768371378	snp	A/G	1.65811e-05	0.00287929	intron-variant	BPTF	GRCh38.p7	17:67904857	TAAGTAATTAAAATT[A/G]CATGTCCTGCATAAT	2186
rs768373563	in-del	-/C			intron-variant	BPTF	GRCh38.p7	17:67925771	TTTCATTTTATAAAA[-/C]CATTTTTTCAAATTC	2186
rs768383666	snp	C/G	1.65529e-05	0.00287683	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67826271	GAGATGGAAGACGAC[C/G]ACGACGACGCCAGTT	2186
rs768408054	snp	C/T	3.29647e-05	0.00405971	synonymous-codon, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67886210	GGAAAACAGTAACAG[C/T]AGCAGTGAACTAAAT	2186
rs768420743	snp	A/G	1.64795e-05	0.00287045	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67911691	AGATGCCACACCTCT[A/G]TCAAGAGCAATGGAC	2186
rs768433496	snp	C/T			intron-variant, missense	BPTF	GRCh38.p7	17:67898412	CATCTCATTAGATGC[C/T]AAGAAGGTATTTTAT	2186
rs768444871	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67906500	TTAAACTCAAGTTCA[A/G]TGAGCCGATTATTTC	2186
rs768462955	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67837866	GACCCTGAGTTTTAC[C/T]TCCCAAATGGCAGGA	2186
rs768491283	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67873970	CCCGGAGCATCTTGT[A/G]ATAGTGGAAAGTAAG	2186
rs768493530	snp	A/G	3.33912e-05	0.00408589	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67826205	CAGGATTCTGAGGAC[A/G]ACGAGGAGGATGAGA	2186
rs768515157	in-del	-/AAC	1.65688e-05	0.00287821	cds-indel, nc-transcript-variant	BPTF	GRCh38.p7	17:67911963	AAGCAAATGGTAAAA[-/AAC]CAAGTCAGCAGAAGA	2186
rs768525742	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67859667	ACTTGCATCGTTTTA[G/T]CTGTTAAAACCAATG	2186
rs768562224	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67919628	GGAAGGTTCAGATTA[C/T]AAAGTGAGTCACTTA	2186
rs768565860	snp	A/G	1.66145e-05	0.00288218	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67874855	GCCAAAAAGGGAGAC[A/G]TTGATAATGTTAAAA	2186
rs768583440	snp	A/G	3.7594e-05	0.00433539	intron-variant	BPTF	GRCh38.p7	17:67909568	GTAAATTATCGTTAC[A/G]TGGTTCTTTTTAGCC	2186
rs768598120	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67830414	GAATGAACCATAGAT[C/T]CAAATTCAAGCAGAA	2186
rs768617273	snp	A/G			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67886627	AGTTTGGTGTGTAAC[A/G]TTTTAGATCTTTCTG	2186
rs768671988	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67894363	AGACAGAGTCTTGCA[C/T]TGTTGCCCAGGCTAG	2186
rs768681762	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67927648	CTGAATCTCACCGCT[A/G]AGCAGCATGGTGTTT	2186
rs768703372	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67845388	ATCATTTCTTTGTTA[A/G]TTATCTGGCATTTGA	2186
rs768723066	snp	C/G	2.47442e-05	0.00351731	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67826058	GGCGGCGGCCACCTG[C/G]CCCGGACCACCGCGG	2186
rs768736219	snp	C/G	1.64885e-05	0.00287123	missense	BPTF	GRCh38.p7	17:67932010	CGAACACCTGTGATG[C/G]TACAGCCAGGTATTT	2186
rs768748140	in-del	-/CACTTTTTTAGAAACGACTGGAG	1.70977e-05	0.00292379	intron-variant	BPTF	GRCh38.p7	17:67928344	ATGTTTCCTCTCCTT[-/CACTTTTTTAGAAACGACTGGAG]CAGCAGAAGCCGACA	2186
rs768756792	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67844773	TTTGAGACGGAGTTT[C/T]ACTCTTGTTGCCCAG	2186
rs768780576	snp	G/T	1.6684e-05	0.00288821	intron-variant	BPTF	GRCh38.p7	17:67924510	CCAGATGCCTAACAG[G/T]CTAGTTTCTGATAAG	2186
rs768786451	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67931371	CTAGCTTCTTGGGAG[C/G]CTGAGGCAGGAGGAT	2186
rs768814391	snp	A/G	3.29457e-05	0.00405854	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67894085	ACCCAGAGAATTTGC[A/G]TTGGCTTTAGCCATT	2186
rs768814937	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67838084	TTAGGTTACCAATTA[A/G]TAGATATTTCAGGTT	2186
rs768835191	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67908494	TGTCACTGACCACTT[-/T]TTTTTTTTTTTTTTT	2186
rs768837896	snp	A/G	1.65367e-05	0.00287543	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911378	TTTATCCAAAAGATC[A/G]AGTGTTAGATGATGT	2186
rs768839258	in-del	-/GAC/GACGAC	0.0145536	0.0840558	cds-indel, nc-transcript-variant	BPTF	GRCh38.p7	17:67826264	CCGGAGGAGATGGAA[-/GAC/GACGAC]GACGACGACGACGAC	2186
rs768855910	snp	A/G	1.65938e-05	0.00288039	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67911973	TAAAAAACCAAGTCA[A/G]CAGAAGAAATTAGAG	2186
rs768892536	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67855163	AAACTTAGCCAGGTG[G/T]GGTGGCGCACACCTG	2186
rs768896179	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67914056	ATAAACACTGAAAAC[A/G]TGAGAGTTCTGGGAA	2186
rs768934613	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67831393	AAAATGAGAGCCAAA[A/G]GGGTTATGAAAAAGT	2186
rs768946380	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67882138	CCGTGCTGGCCGGAC[A/T]TCTTGCTTTTTAGCA	2186
rs768960868	snp	C/T	1.64784e-05	0.00287035	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67920066	TTAAGAGGAGAGATG[C/T]TGGTCCTTATGGCAT	2186
rs768974214	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67920296	TATTAAAGTAATAAA[C/T]ATATCAAGATTCTGG	2186
rs768980690	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67839399	CATCTTTTAAGATGA[G/T]CATATAGTTTTTCTC	2186
rs769003623	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67880693	CCAGGCTGGATTGCC[A/G]TAAAGTGGCCATAAC	2186
rs769020340	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67833094	GAGCCACTGCGCCCC[A/G]CCTGATTTGCCTCTT	2186
rs769030810	in-del	-/TTA			intron-variant	BPTF	GRCh38.p7	17:67951562	GAAAATAGTTGTAGT[-/TTA]TATCCTTTATGTATA	2186
rs769073290	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67902048	GAAAGAAAATCTGCC[A/T]CTGGCACACCCACCA	2186
rs769100141	snp	C/T	1.64727e-05	0.00286986	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67854262	TGCTGATCTGAAAGA[C/T]AGCGTTAATTCCACA	2186
rs769104467	snp	C/T	1.76222e-05	0.0029683	missense, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67875729	GTGGCATCTGAGCTC[C/T]CCCAGGATGTGCCAG	2186
rs769128743	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67827604	TGTGAGGAAAAAAGA[C/G]CTTTTTTTTCGTTGA	2186
rs769143663	snp	A/C/T			intron-variant	BPTF	GRCh38.p7	17:67855931	ACGGAATCTTCGCTG[A/C/T]CTATGGTGTTCTGCA	2186
rs769181170	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67868629	GTAAGATTCTGAAAG[G/T]ACACTTTTAAGTGCC	2186
rs769182834	snp	A/G	3.3295e-05	0.00408	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67893633	TGTCCATGGGTCCAA[A/G]GTTCTTACCATATCT	2186
rs769196919	snp	C/T	3.29592e-05	0.00405938	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911702	CTCTGTCAAGAGCAA[C/T]GGACTTTGAAGGAAA	2186
rs769197570	in-del	-/ATATC			intron-variant	BPTF	GRCh38.p7	17:67859826	GTTCTGTTTCCTAAT[-/ATATC]AGTATCAGTCTACGA	2186
rs769225236	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67938617	GGAATAATTGGCTTA[C/T]AGTTTGGGGGGAAAA	2186
rs769269947	snp	A/G/T			intron-variant	BPTF	GRCh38.p7	17:67851044	TATATATATTTACAC[A/G/T]CACCAGACTATGGAG	2186
rs769279013	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67852194	GACGTTGTATTTATA[C/G]AAGACTATGAGTAGT	2186
rs769299474	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67936243	AGGCAATCGTCTTGC[C/G]TAAGTAGCATTTACC	2186
rs769321239	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67836603	AGGTTTATGAACTTA[C/T]TCATAGAGCCTCAAA	2186
rs769322637	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67851401	TGGTGACCATTGTTT[A/G]TGTGCACGTTCAATT	2186
rs769329330	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67923402	GCAGTAAAGTCCTAG[C/G]TTGACTTTACTCCAC	2186
rs769338145	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67901596	ATAGTCTAATACAAA[C/G]AAGACAAAGGATTTG	2186
rs769354664	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67919767	ATTATTTTGATTGAG[C/T]ATTGCCACCAGGAGC	2186
rs769355818	snp	A/C	1.73072e-05	0.00294165	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67913169	CTTCTCCTAGACCGA[A/C]CTTTGGCATCACTTG	2186
rs769407220	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67935060	CAGTTGAAATAAATC[A/G]GTGAATAAAACAAAC	2186
rs769414401	snp	A/G	1.84869e-05	0.00304024	intron-variant	BPTF	GRCh38.p7	17:67874772	GGTACTGTTCTATTT[A/G]GTTATATATAGGAAT	2186
rs769468232	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67840965	CCTGTCAGTGCCTTG[C/G]GTTTCATTCTCTTAA	2186
rs769469510	snp	C/T	1.65614e-05	0.00287757	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67874883	AAAGCCCAGAAGAAA[C/T]AGAAAAAGACAAGAA	2186
rs769526468	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67874167	GAGTGCGTACTGATA[C/T]ACCGTGTGTTCTGTA	2186
rs769526523	snp	A/G			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67888311	CAGTAGATCTGGGCC[A/G]GGCTCGGTGGCTCAC	2186
rs769548585	snp	A/C	5.3905e-05	0.0051913	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67909584	TGGTTCTTTTTAGCC[A/C]AAAATAATATGGATG	2186
rs769552743	in-del	-/CTTTC			intron-variant	BPTF	GRCh38.p7	17:67906662	TTTGCACTCTCTTCT[-/CTTTC]TTCAGCCAGACCTTT	2186
rs769559184	snp	C/T	1.67326e-05	0.00289241	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67854736	AAGTCGGAGGAAATA[C/T]TGGTTCTTGAACCGA	2186
rs769576037	snp	C/T	1.7565e-05	0.00296347	intron-variant	BPTF	GRCh38.p7	17:67853907	AATGATGTAATGTAT[C/T]GATTTGTAATGATGT	2186
rs769576468	snp	A/G			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67886785	CTCAGTGATACATGG[A/G]GAGAATCTTTTTGTG	2186
rs769591312	snp	C/T	3.30098e-05	0.00406249	intron-variant	BPTF	GRCh38.p7	17:67924541	TTTCTCCTTTTTTTC[C/T]TGCAGAGTGGAGAAA	2186
rs769599803	snp	A/G	1.65466e-05	0.00287628	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67909719	AAAGGAGCAGACCAA[A/G]ATGAAATGGATATCT	2186
rs769607707	snp	G/T	1.65718e-05	0.00287848	missense, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67886314	CTATTCAGGAAGAGA[G/T]AGGTAAGAATATACT	2186
rs769615394	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67861045	CTGGACCTGTCCGCA[A/C]GGCAGGCACCTCAAA	2186
rs769661089	snp	A/G	1.65488e-05	0.00287647	missense, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67891909	GGAGCTGGAAAAGGA[A/G]CATCTGGCTCAACTC	2186
rs769698489	in-del	CCAAAAAAAAAAAAA/GTCTCC			intron-variant	BPTF	GRCh38.p7	17:67858554	AGTGAGACTCTGTCT[CCAAAAAAAAAAAAA/GTCTCC]AAAAAAAAAAGTTTA	2186
rs769701603	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67845607	AGGGAGACCCCATCT[C/T]GACAGAAAATTTAAA	2186
rs769729978	in-del	-/TT			intron-variant	BPTF	GRCh38.p7	17:67924283	CCAGCTCCGACTAAC[-/TT]TTGTATTTTTAGTAG	2186
rs769736049	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67907515	TACCCGCCACCACGC[C/T]GAGCTAATTTTTGTA	2186
rs769753272	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67875439	TACTTGCTTTAAAAT[A/G]GCCGTTCAATGGAAG	2186
rs769754197	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67868774	GGATAGCTGTATCCA[A/G]CCTTGTTCTCACATA	2186
rs769784919	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67847134	AAAGGAAGTAATAAT[A/G]GTATCTATTTTATGG	2186
rs769811161	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67882319	CACTGTCCCTATGCT[A/T]TTTTGGTGGGTAGTG	2186
rs769830035	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67833487	ACATTCGTGTACATG[G/T]TTTTATCTGTACGTA	2186
rs769879193	snp	A/T	1.64825e-05	0.00287071	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67920111	GTATCAGGAAAATCA[A/T]TTGTCCCATTGGAGT	2186
rs769883480	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67831482	GTCTTGCACACAGTT[C/T]GTGCTTTTCTATTCT	2186
rs769915111	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67883948	TTATAAATTTGTATT[C/T]CCTCCTCTTCTCACA	2186
rs769920559	snp	C/T	1.66288e-05	0.00288343	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912536	CATCACCTATTACTT[C/T]TGAAGAGGAATCTAA	2186
rs769925265	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67857840	TGCCCCGGCTAGAGT[A/G]CAGTGGCGCGATCCT	2186
rs769949554	snp	G/T	1.65482e-05	0.00287643	missense, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67875635	TGCAACTTCAGAAGA[G/T]ACTAGTCCCTCTGAA	2186
rs769959435	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67961441	TGAAAACTGAAATTC[A/C]AGTCCTGAACATCCT	2186
rs769961728	snp	G/T	1.65168e-05	0.00287369	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911562	CAGTGCAGATGATAT[G/T]GGTACTTTGATCTGT	2186
rs769963644	snp	A/C	3.31472e-05	0.00407093	intron-variant	BPTF	GRCh38.p7	17:67894216	TGGACTCCCTTTTGA[A/C]ATACTAGCCTATTAA	2186
rs770025566	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67902783	CTCCCACATCTTTTC[A/G]GCATCACTACCCCAA	2186
rs770032085	in-del	-/C			intron-variant	BPTF	GRCh38.p7	17:67826388	CACCTCCTCTGCCCT[-/C]CCCCCCTTGCTCACT	2186
rs770051470	snp	A/C	3.29457e-05	0.00405854	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67854287	TCCACACTGTATTTC[A/C]TAGATGGGATGACGT	2186
rs770066938	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67931583	TATGGTCTGGAGCTT[A/G]CAGAAAGTGCGACTC	2186
rs770071672	snp	A/C	1.67147e-05	0.00289086	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67912177	TTCTGAGAGTAGAGT[A/C]GTAAGTGGTAATGTT	2186
rs770114725	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67903784	TTCTATGCATGAATT[C/G]TTAGGTTACACCGGA	2186
rs770124718	snp	C/G	1.6727e-05	0.00289193	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912279	TGCTATAAGGCCATT[C/G]ATTAATGGTGATGTC	2186
rs770159739	in-del	-/TTG			intron-variant	BPTF	GRCh38.p7	17:67847013	GCTGGACTTGTGGGT[-/TTG]TTGTTGTTTTTTTGT	2186
rs770160887	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67915577	TGTACCTCTACACCC[C/T]TTCCCTCCAGTCATA	2186
rs770187025	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67975072	TAAAAGAAACTCTTA[C/T]CACTCCGGAGATTCC	2186
rs770204988	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67890762	TATTTTCCCCAAAAT[A/G]CATAGCCAGTTTTCC	2186
rs770212761	in-del	-/GA			intron-variant	BPTF	GRCh38.p7	17:67977291	AGGCCAAGGTGGGTG[-/GA]TCACTTGAGGTCAGC	2186
rs770227764	snp	A/G	1.6525e-05	0.00287441	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911050	TACAAAAAGAAAACA[A/G]AATCATCCAAACTAG	2186
rs770242305	in-del	-/TG			intron-variant	BPTF	GRCh38.p7	17:67840460	TGCTGCTGCTCCTCT[-/TG]TTGTTGTTGTTGCTG	2186
rs770258772	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67840346	TCCTGGGCTCAAGCA[A/G]TCCACCTGCCTCGGC	2186
rs770259337	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67939615	AGGTGAGGTTGCTCA[C/T]GCCTGTAATCCCAGC	2186
rs770270063	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67828031	CCGTCTTCCAGACTC[A/G]AGCGATTCTCCTGCC	2186
rs770278826	snp	A/G	1.64806e-05	0.00287054	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67893477	GGGTCAAGAAGGGAA[A/G]TATCGCGTCTACCAC	2186
rs770309921	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67855974	TACGCCCTTGTGTGG[A/G]CTGCTTTCATCCACG	2186
rs770323373	snp	G/T	1.64846e-05	0.0028709	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911807	AAGAAGATATGATTG[G/T]TCAGAATAGCAATGA	2186
rs770343953	snp	C/T			intron-variant, utr-variant-5-prime	BPTF	GRCh38.p7	17:67889244	TCAGTTTAGTTCTTT[C/T]TCTCCATTCCTTTAA	2186
rs770369061	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67923472	TCCTCTCTCTCTGTC[-/T]TTTTTTTTTTTTTTT	2186
rs770378445	snp	A/G	5.27273e-05	0.00513428	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67909593	TTAGCCAAAAATAAT[A/G]TGGATGAAAATATGG	2186
rs770399904	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67909772	CCAAGGTAAGGAGAG[C/T]CAGCTGTGGAGGGCA	2186
rs770400803	snp	C/T	1.74668e-05	0.00295518	intron-variant	BPTF	GRCh38.p7	17:67853917	TGTATTGATTTGTAA[C/T]GATGTCACGTCTTTA	2186
rs770433583	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67876367	ACGACTTCCATTTGA[A/G]TACTGGTCAGCAGTG	2186
rs770454041	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67860412	TTTATAGAAATTAAG[-/T]TTTCTGTTATTGCTT	2186
rs770460475	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67907701	TGACCACTTTTTTTA[A/G]TCCTGCAGTGTTTTA	2186
rs770461769	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67838163	CAGGAAAGCAGCCAT[A/G]GACAATAAGTAAACA	2186
rs770465480	snp	A/G	1.64879e-05	0.00287118	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67929431	CAGCCCAGGACAGCA[A/G]CAGTCACAATTAGGC	2186
rs770466408	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67921429	TACTTGGGAGGGTGA[A/G]GCGGGAGAATCACTT	2186
rs770505841	snp	A/G	5.03931e-05	0.00501936	intron-variant	BPTF	GRCh38.p7	17:67854810	ATTTAAAATTAGACT[A/G]GTTTCCTTCGTGATT	2186
rs770524267	snp	G/T			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67888461	CGGGCATGGTGGTGT[G/T]TGCCTGTAATCCCAG	2186
rs770557082	snp	A/G	1.67758e-05	0.00289614	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67909750	CAAAGATTACTGAGA[A/G]GAAGGACCAAGGTAA	2186
rs770595988	snp	A/G	3.30387e-05	0.00406427	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911924	CTGGAAACTGTGAGG[A/G]CAGGCTGCCGGTCAA	2186
rs770630894	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67937518	GGACTCACTAACAAG[A/G]TGAAATTTGGATAAA	2186
rs770640196	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67867173	CATTCCACTGTAAAT[G/T]AGGGATGCTATACAT	2186
rs770642819	in-del	-/TTTT			intron-variant	BPTF	GRCh38.p7	17:67881493	TTCCATAATCAAGGT[-/TTTT]TTTTTTTTTTTTTTT	2186
rs770661436	in-del	-/TG			intron-variant	BPTF	GRCh38.p7	17:67892856	GCTGAATAAGGCCAC[-/TG]TTTATCTGATAGTCC	2186
rs770674695	snp	A/G	1.97802e-05	0.00314479	intron-variant	BPTF	GRCh38.p7	17:67892065	TTAAAACAAAAATCT[A/G]TGGAATGTGAGATAA	2186
rs770701026	snp	C/T	1.65405e-05	0.00287576	missense, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67891918	AAAGGAGCATCTGGC[C/T]CAACTCGAATCATCA	2186
rs770714328	snp	C/T	3.33089e-05	0.00408085	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912584	TTGATGAAAATGGTC[C/T]GCCCATCAACAAAAA	2186
rs770728205	snp	C/T	0.000188626	0.00970965	upstream-variant-2KB	BPTF	GRCh38.p7	17:67825493	GCCTGCGGCCGCTGT[C/T]GGTTCCCCCAGTCAC	2186
rs770729719	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67827362	CCCTCTTCTGTTTTC[G/T]CACAGAAAGTTTCTC	2186
rs770754023	snp	A/C	1.67365e-05	0.00289275	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67866495	AATGAAAATGAAAAG[A/C]AAATTTGGTATTACA	2186
rs770795291	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67933414	ATCTCTACAAAAAAT[A/C]AAAATTTAGCCAGGC	2186
rs770807209	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67884021	TAACATTTAATCTTG[A/G]AGATCATTTTATGTG	2186
rs770809457	snp	C/G	1.64781e-05	0.00287033	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67866633	ATGGACATAACTGAA[C/G]ACCTGACCAATAAGG	2186
rs770825293	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67847361	CTCTACTAAAAATAA[C/T]AAATTAGCCGGGCGT	2186
rs770862701	snp	A/G			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67897151	GACGAACATGGAGAA[A/G]CCCTTTCTCTACTTA	2186
rs770880281	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67862663	TGCAGCTGCTATAAC[A/C]AAGTACTATACCAAA	2186
rs770887877	in-del	-/CCC	1.70551e-05	0.00292015	intron-variant	BPTF	GRCh38.p7	17:67866446	ACATATAAAGTATTT[-/CCC]CCCATTTTTAAACAG	2186
rs770918090	snp	C/T	0.0001831	0.00956642	intron-variant	BPTF	GRCh38.p7	17:67923032	GCTATTTGAAGATTT[C/T]ATCACTTCAGAATCA	2186
rs770927278	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67849391	GGGCCTGAGATTCTG[A/T]ATTTCTCTCAAACAT	2186
rs770936416	in-del	-/AG			intron-variant	BPTF	GRCh38.p7	17:67908182	TTTTATGTGTGTGAC[-/AG]AGTCTTGCTCTGTCA	2186
rs770940722	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67835245	AAAATGAAAAGTTAG[G/T]TTCTCCTGTGGCACT	2186
rs771031194	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67872699	CAACAGAGTGAGATT[C/G]TGTCTCAAAAAAAAA	2186
rs771036982	snp	A/C	1.65111e-05	0.0028732	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67904833	TTACAGAAAGTCGTT[A/C]GAAGGAAGTAAGTAA	2186
rs771040209	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67884948	CTTCATATAGTTTTA[C/T]TTTACATTTCTCATA	2186
rs771043587	snp	A/G	1.66515e-05	0.00288539	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912322	TTTAATGAAAGAAAC[A/G]GCTCCGAAACAAAAT	2186
rs771057436	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67881589	GCTTACTGCAACCTC[C/T]GCCTCCCAGGTTCAA	2186
rs771110616	in-del	-/CTC			intron-variant	BPTF	GRCh38.p7	17:67845111	TGTATAAGTGCACGT[-/CTC]CTCCTCAGCACATCT	2186
rs771112320	snp	A/C	1.65457e-05	0.00287621	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912392	GAGATAGCCTTGAGA[A/C]CCTGCCATCAACCAA	2186
rs771123647	snp	A/G	2.26288e-05	0.00336361	intron-variant	BPTF	GRCh38.p7	17:67875776	ATCAATGCCTCTGTA[A/G]TGGGGGGAATCCTTC	2186
rs771126708	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67884026	TTTAATCTTGGAGAT[A/C]ATTTTATGTGTGAAC	2186
rs771145621	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67890952	GGAAATTTAACAGTG[A/G]TGCAGTAGTTTTAGA	2186
rs771156886	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67939732	ACAAATACAAAAAAT[G/T]AGTCGGGTGTGGTGG	2186
rs771168500	snp	A/G			missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911482	GACCTTGCCAGTAGA[A/G]GCCAGGAACCCAGTA	2186
rs771178805	snp	A/G	1.64898e-05	0.00287135	missense, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67886175	ACTAGTGCTACCACT[A/G]CCTCCATCCAGCCTA	2186
rs771199467	snp	G/T	1.65649e-05	0.00287788	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67911103	TAAACAGTTTACACT[G/T]GAAGAAAAACAGCGA	2186
rs771231934	snp	G/T	1.64727e-05	0.00286986	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67854482	TTGATGTCTGAAGGG[G/T]TGATACAGTATGATG	2186
rs771240127	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67905086	AGAAGACGCCTCAGC[C/T]GCCTGATTATCATTT	2186
rs771249433	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67892131	ATTTGTAGAAATTTG[C/T]AGACCTATTTTTGAA	2186
rs771253097	snp	A/G	1.67052e-05	0.00289004	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911195	CAAAAAATCTCTCTG[A/G]ATCACCAGTAATAAC	2186
rs771285162	in-del	-/AA			intron-variant	BPTF	GRCh38.p7	17:67869291	AAAAATAGAAAAAAC[-/AA]AAAAATATTTTCTGT	2186
rs771285295	snp	A/C	1.64923e-05	0.00287156	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67854695	AATAAACCATATATT[A/C]GACATGAACCTATTG	2186
rs771291435	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67903991	GAAACTTTGAATACT[C/T]ACTAATTTTATTTTT	2186
rs771305882	snp	C/G	1.66729e-05	0.00288724	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67893660	ATCTACTCTGAGACT[C/G]ACTATCACCCAATTA	2186
rs771346510	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67855000	TGCCTAGGCTAGGAA[A/G]TAGAATGTTTCTAGT	2186
rs771352923	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67925206	TATTTATTATCTTTA[C/G]AGTTTCATAAGTAAT	2186
rs771357346	snp	C/T	1.65373e-05	0.00287548	intron-variant	BPTF	GRCh38.p7	17:67894013	AGTGAAATAATTTCT[C/T]TCATTTCTTCTGAAA	2186
rs771385420	snp	C/T	1.65332e-05	0.00287512	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67929454	AATTAGGCCCAATAC[C/T]TCAGGCTCTGGAGGA	2186
rs771406246	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67927122	TGTCAAAGGCAGGAG[A/C]TAGTGGTGCAGGATT	2186
rs771413164	snp	A/G	1.65468e-05	0.00287631	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67874903	AAAGACAAGAATGAG[A/G]CTGAGAATGACTCTA	2186
rs771432074	in-del	-/TTCCCTTTTTC			intron-variant	BPTF	GRCh38.p7	17:67832815	TTTTTGAGGCAGAGT[-/TTCCCTTTTTC]CTCGCTCTGTCACCT	2186
rs771437944	snp	A/G	3.34997e-05	0.00409252	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912268	GTTAAAGAATCTGCT[A/G]TAAGGCCATTCATTA	2186
rs771474327	snp	C/T	4.94181e-05	0.00497057	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67854076	TGTCATTGCCATTTA[C/T]GAGGTACTGCGGAAC	2186
rs771478073	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67878222	TCCAGATGTTGCTAG[C/T]AGTAGCAGCTTATTC	2186
rs771548849	in-del	-/TTG			intron-variant	BPTF	GRCh38.p7	17:67881856	GGGGATTTTGGGTTT[-/TTG]TTTTTTTTTTTTTTT	2186
rs771581740	snp	A/C	1.64773e-05	0.00287026	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67928505	AAAATGGTACTAACT[A/C]CTAAAGTTGGATCTC	2186
rs771588338	snp	C/G			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67897225	ACATGCCTGTAATCC[C/G]AGCTACTCGGGAGGC	2186
rs771614816	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67890540	AGCCAGTCCTGGGAC[A/G]GTCACTGTGGCCAGC	2186
rs771660851	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67876678	GGACATGATATCATG[C/T]GCCTGTAATCCCAGC	2186
rs771675314	snp	C/T	1.68684e-05	0.00290412	splice-donor-variant	BPTF	GRCh38.p7	17:67909763	GAAGAAGGACCAAGG[C/T]AAGGAGAGTCAGCTG	2186
rs771675585	snp	A/C	1.66944e-05	0.0028891	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912127	AAAGATAATAAACCC[A/C]AAATATATTTGAAAG	2186
rs771701568	snp	A/G	1.65261e-05	0.0028745	intron-variant	BPTF	GRCh38.p7	17:67893323	TTAGATGAAATTCAC[A/G]TCTTTGATTGACATA	2186
rs771774204	snp	C/G	1.66499e-05	0.00288525	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912693	ATCAAAAACTGTGAT[C/G]AAGGTAGAAAAAGGC	2186
rs771776112	snp	A/G	0.000584368	0.0170834	intron-variant, synonymous-codon	BPTF	GRCh38.p7	17:67929047	AGTCACTATGGCAGG[A/G]AAAGTAATTACCAAA	2186
rs771790818	snp	A/G	1.65045e-05	0.00287263	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67911589	CTGTAAGAACAAAAA[A/G]CCGCTCATACAGGAG	2186
rs771815998	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67847370	AAATAATAAATTAGC[C/T]GGGCGTGGTGGCACA	2186
rs771831392	snp	A/G	3.31994e-05	0.00407414	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912808	ACACCCTCCACAGGC[A/G]GCAGTGTGGACATCA	2186
rs771838203	in-del	-/TT			upstream-variant-2KB	BPTF	GRCh38.p7	17:67825062	GCCCCTCTCCGCGAC[-/TT]TTTTTTTTCTTTCTC	2186
rs771905109	snp	C/T	1.79049e-05	0.00299201	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67826083	CCGCGGCCCGGAGGG[C/T]CGTCAACAAAGTGGT	2186
rs771917318	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67933529	AAGTATGCTCATGCT[A/G]CTGCACTCCAGCCTG	2186
rs771921517	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67932888	CCTACTGATACTGGG[A/C]AGAATAAAATTCAAT	2186
rs771931849	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67917951	CGAGTAGCTGGGACT[A/G]CAGGCACCCACCACC	2186
rs771957019	snp	A/T			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67898051	CTCCAATACTAGGAG[A/T]TTACTAATACCATAC	2186
rs771970017	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67835451	ATTTGCCCTAAATCC[C/T]GCACAGCTTGGGTAG	2186
rs771970450	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67934463	GGTGGGGGTTGCAGT[C/G]AGCGGAGATTGCACC	2186
rs771978315	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67838250	CCATAGTTTATTCAC[C/T]CCATTTTTGAGCTCT	2186
rs771983682	snp	A/G	6.59174e-05	0.00574059	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911669	TGCCTAAAAGTACCA[A/G]TGACAGAGATGCCAC	2186
rs771984251	in-del	-/TAAA			intron-variant	BPTF	GRCh38.p7	17:67937436	GGAGGAACGATAATG[-/TAAA]TTTAGAGTTGGGATT	2186
rs772002069	in-del	-/TTAT			intron-variant	BPTF	GRCh38.p7	17:67868131	TAATTCAATGTCACC[-/TTAT]TTATTTTGTTACTCA	2186
rs772049054	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67885257	CTTTTAAGAACTATA[C/T]TCTTAGTGATACTAT	2186
rs772066206	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67865039	TCTCGATCTCCTGAC[C/T]TTGTGATCCGCCCGC	2186
rs772074851	snp	A/T	1.66167e-05	0.00288237	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912517	GAAGTTAAGAAAGTT[A/T]CTTCATCACCTATTA	2186
rs772099790	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67939834	GCAGTGAGCCAAGAT[C/G]ACGCCACCGCACTCC	2186
rs772103761	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67905304	TCCCAGCTACTGAGG[A/G]GGCTGAGGCAGGAGA	2186
rs772123338	in-del	-/GAT	1.66955e-05	0.0028892	cds-indel, nc-transcript-variant	BPTF	GRCh38.p7	17:67911241	GTGTCAGAGTGACTC[-/GAT]GAGACAAGAACAGAG	2186
rs772136124	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67851419	TGCACGTTCAATTGA[A/G]TTCAGATTTAATATT	2186
rs772172883	in-del	-/C			intron-variant	BPTF	GRCh38.p7	17:67840458	GTTGCTGCTGCTCCT[-/C]TTGTTGTTGTTGTTG	2186
rs772175789	snp	C/T	6.61967e-05	0.00575273	synonymous-codon, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67886303	TACACCTGTCTCTAT[C/T]CAGGAAGAGATAGGT	2186
rs772176333	in-del	-/TTTTT	2.96696e-05	0.00385148	intron-variant	BPTF	GRCh38.p7	17:67886369	TTTTTCTTTTTTTTC[-/TTTTT]TTTGTGTGTGTGTGT	2186
rs772176905	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67873875	TAACATCATTCTCCA[A/G]TTTGTTCTTCAAAAA	2186
rs772189308	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67979762	AGAAATTACCCTGGC[C/T]GGGCGCAGTGGCTCA	2186
rs772206794	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67836251	ACTTCTTTCTACTCA[C/T]GGATATGTTCTGTAA	2186
rs772220317	snp	C/T	1.68624e-05	0.0029036	intron-variant	BPTF	GRCh38.p7	17:67931889	AAGCATTTTAATTCA[C/T]TGTTCTTTGTGTCAT	2186
rs772222601	snp	C/T	1.67119e-05	0.00289062	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911200	AATCTCTCTGAATCA[C/T]CAGTAATAACGAAAG	2186
rs772248225	in-del	-/CTGTT			intron-variant	BPTF	GRCh38.p7	17:67836491	GGAATTTCTCTTGTC[-/CTGTT]CTAATTCTTGCATAG	2186
rs772255159	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67929192	TTTTCATCTCCTTTT[C/T]ACTGATTTCAGTCCT	2186
rs772257974	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67903364	TCCATGCAATGGAAT[A/C]TTTTTTAATTCCTTA	2186
rs772273169	snp	G/T	1.82563e-05	0.00302123	intron-variant	BPTF	GRCh38.p7	17:67913207	GTACTTTAAAATGTA[G/T]TTGGGGGAGGGAGAA	2186
rs772293700	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67831213	GCACTTTAGAGTTCT[C/T]CAGGCCTTGACACAT	2186
rs772347271	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67906203	CTCCTGCCTCAGCCT[C/T]CCGAGTAGCTGGGAC	2186
rs772374289	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67879554	TAATGGCTATCTTAG[G/T]CCATTTGTGTTGCTG	2186
rs772374423	snp	A/G	0.00028066	0.0118428	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67893440	TGATCATGAAAGGAA[A/G]TATCAACAATTATTT	2186
rs772380385	in-del	-/T			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67897823	ATTTTATAATTATTG[-/T]TTCTGTTAGTGTGAA	2186
rs772401732	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67852902	GCACTTTGGCAGGCC[A/G]AGGTGGGTGGACCAC	2186
rs772452129	snp	A/T	1.65037e-05	0.00287256	intron-variant	BPTF	GRCh38.p7	17:67894180	GGTAAATGAATTCTG[A/T]GCCTTGTAAATGATG	2186
rs772470739	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67900265	AAGTACCACAATGCC[C/T]GGCTAATTTTCGTAT	2186
rs772491291	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67906008	TACATATGTCACAAA[C/G]CTGCACGTTGTGCGC	2186
rs772494489	snp	C/G	3.30967e-05	0.00406783	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912388	TACCGAGATAGCCTT[C/G]AGACCCTGCCATCAA	2186
rs772506715	snp	A/G	1.65578e-05	0.00287726	missense, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67875609	GCAAATCTTGGCGAC[A/G]ACACAACAAATGCAA	2186
rs772512709	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67830288	TGGAATTTTAAAACT[C/T]GGAACCTCTGATAAC	2186
rs772569850	snp	C/T	1.73996e-05	0.00294949	intron-variant	BPTF	GRCh38.p7	17:67853923	GATTTGTAATGATGT[C/T]ACGTCTTTATCTACA	2186
rs772571922	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67868570	TTGGCCACAGAGGGC[C/T]GACTATAGTGCCTTT	2186
rs772572658	in-del	-/G	3.34725e-05	0.00409086	frameshift-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67912190	GTAGTAAGTGGTAAT[-/G]TTGAACCAAAGGTTA	2186
rs772593161	in-del	-/AGGCAGAGCTTGCAGTGAGCAGAGGTCGCGCCAC			intron-variant	BPTF	GRCh38.p7	17:67847442	TAGCGTGAACCGGGG[lengthTooLong]TGCACTCCAGCGTGG	2186
rs772627239	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67924250	ATGAGCCACCGCACC[C/T]GGCCTGAGCCACTGT	2186
rs772718334	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67936481	TACTATGGATACACA[A/G]AGCCTTTGTTGCATA	2186
rs772721146	snp	C/T	6.59185e-05	0.00574064	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911720	ACTTTGAAGGAAAAC[C/T]GGGATGTGACTCTGA	2186
rs772736510	snp	C/G/T	6.59319e-05	0.00574127	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911801	GCAGTGAAGAAGATA[C/G/T]GATTGTTCAGAATAG	2186
rs772739109	snp	A/G	1.65564e-05	0.00287714	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67874888	CCAGAAGAAACAGAA[A/G]AAGACAAGAATGAGA	2186
rs772746427	snp	A/G	1.64852e-05	0.00287094	synonymous-codon, intron-variant	BPTF	GRCh38.p7	17:67924562	AGTGGAGAAAGAAAA[A/G]GCACAAGCAGTTGAG	2186
rs772759476	snp	A/G	4.96019e-05	0.00497981	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67911934	TGAGGACAGGCTGCC[A/G]GTCAAGGGGACTGAA	2186
rs772791706	snp	A/G			upstream-variant-2KB	BPTF	GRCh38.p7	17:67823878	CAGTGGTGCGATCTC[A/G]GCTCACTGCAACCTC	2186
rs772810466	snp	C/G	3.32392e-05	0.00407658	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67826213	TGAGGACGACGAGGA[C/G]GATGAGATGGAAGAG	2186
rs772812714	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67936307	AATGCTGCAGGAACA[A/G]TTGATAAGATTTAAT	2186
rs772890962	snp	C/T	1.64825e-05	0.00287071	missense, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67886245	CCCAGAGTGAATCTG[C/T]TAAGGCAGCTGATGA	2186
rs772894827	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67860020	AATACTTATGTTTGT[C/T]AATAAAACTGTTCAT	2186
rs772901349	snp	A/G	1.79101e-05	0.00299244	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67909585	GGTTCTTTTTAGCCA[A/G]AAATAATATGGATGA	2186
rs772907736	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67869264	CATTGAATTAAAATA[-/T]TTTTCAGAATAAAAA	2186
rs772925368	in-del	-/AGTT			intron-variant	BPTF	GRCh38.p7	17:67948837	TACACAAAATGAAAA[-/AGTT]AGCCAGATGTGGTGG	2186
rs772928787	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67966502	GTTCATTGATGTAGT[A/G]ACTCAACCAGGAAAC	2186
rs772936265	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67862062	TTCACTGCAACCTCC[A/G]CCTCCCAGGTTCAAG	2186
rs772941321	snp	G/T	1.66178e-05	0.00288247	intron-variant	BPTF	GRCh38.p7	17:67886329	TAGGTAAGAATATAC[G/T]TCATCCATTCCTTTA	2186
rs772941425	in-del	-/A			intron-variant	BPTF	GRCh38.p7	17:67869827	CTCTACTAAAAATAC[-/A]AAAAAAAAAAAAAAA	2186
rs772943176	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67907558	ACGGGGTTTTGCCAT[A/G]TTGGCCAGGCTGATC	2186
rs772996270	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67906661	CTTTGCACTCTCTTC[A/T]CTTTCTTCAGCCAGA	2186
rs773030744	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67865122	GTTGATCATTCCTAA[C/T]CTGAAAATCTGAAAC	2186
rs773033875	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67874188	GTGTTCTGTACACTG[C/T]GGTCCTTCTGTATCC	2186
rs773034001	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67845744	CACCACTGCACTCTA[A/G]CCTGAGCGACAGCAA	2186
rs773060656	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67880833	AACCCTCTATCAGAG[A/G]ACATTCTATGCATGA	2186
rs773063236	snp	C/T	3.42038e-05	0.0041353	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67854748	ATACTGGTTCTTGAA[C/T]CGAAGACTCATAATG	2186
rs773083223	snp	C/T	5.11635e-05	0.00505758	intron-variant	BPTF	GRCh38.p7	17:67866446	ACATATAAAGTATTT[C/T]CCCCCATTTTTAAAC	2186
rs773092668	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67831512	TGCTCACCCACGGGC[A/G]TGTTTGGAAGTTTGT	2186
rs773118573	snp	A/G	1.65272e-05	0.0028746	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67928378	GGAGCAGCAGAAGCC[A/G]ACAGTGATTGCAACT	2186
rs773159697	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67838330	TGAGTTTTACAAATA[A/G]TGCTTCTGAAAATCT	2186
rs773171191	snp	A/G	1.64732e-05	0.0028699	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67854123	GATTATCTCCTTTTC[A/G]CTTTGAGGACTTTTG	2186
rs773181187	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67978143	ACGGGCGTGAGCCAC[C/T]GCACCCGGCCATGAT	2186
rs773199408	snp	A/G	4.96241e-05	0.00498092	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67912429	TGACAGTACACAGAC[A/G]ACCACACCCTCAGCA	2186
rs773219849	snp	A/T			intron-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67929734	ATTGCTTTCTAGGAT[A/T]TTATAAAGAAAATTT	2186
rs773241506	in-del	-/ATGTA	1.76086e-05	0.00296715	intron-variant	BPTF	GRCh38.p7	17:67853896	AAATTTGTAGAAATG[-/ATGTA]ATGTATTGATTTGTA	2186
rs773254228	snp	C/T	1.66449e-05	0.00288482	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67912561	ATCTAATCTCAGTAA[C/T]GACTTTATTGATGAA	2186
rs773299098	in-del	-/GAG	0.0831758	0.186198	cds-indel, nc-transcript-variant	BPTF	GRCh38.p7	17:67826118	GATGACCACGAGAGC[-/GAG]GAGGAGGAGGAAGAG	2186
rs773331280	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67871802	ACATTTTGGGTCTCT[C/T]TTTCTTTTTGTTGTT	2186
rs773377445	snp	A/C	3.31044e-05	0.0040683	missense, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67875637	CAACTTCAGAAGAGA[A/C]TAGTCCCTCTGAAGG	2186
rs773383954	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67915671	GTGTGCCCCTTGCCT[C/T]TGATCAGCAACCCCC	2186
rs773395483	snp	A/G	1.67161e-05	0.00289098	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912178	TCTGAGAGTAGAGTA[A/G]TAAGTGGTAATGTTG	2186
rs773405496	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67955061	TTGGGAGGCCGAGGC[A/G]GGCGGATCACGAGGT	2186
rs773414397	snp	C/G/T	1.64958e-05	0.00287187	missense, synonymous-codon	BPTF	GRCh38.p7	17:67931916	TCATTTATAGGTAAT[C/G/T]ACAGGGCCTCAGATT	2186
rs773423558	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67828004	TGTCCTGATCTCGGC[C/T]CACTGCAACCTCCGT	2186
rs773436940	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67914700	GGGAAGCACTCTTCT[C/T]TGAACTCTCCAGGAG	2186
rs773448400	snp	A/G	1.67044e-05	0.00288997	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912290	CATTCATTAATGGTG[A/G]TGTCATCATGGAAGA	2186
rs773493340	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67937971	ATACAAAAAATAGCC[A/G]GGCATGGTGGCGCAG	2186
rs773507500	snp	C/T	0.000102886	0.00717164	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67910888	ACAGATGTGAAGGAG[C/T]TCTTAGATTCTGACA	2186
rs773509857	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67924251	TGAGCCACCGCACCC[A/G]GCCTGAGCCACTGTG	2186
rs773539568	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67829237	TTGCTATTTCATATT[C/G]CTTGCCAGGCATTTT	2186
rs773541934	snp	C/T	1.6473e-05	0.00286988	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67854300	TCATAGATGGGATGA[C/T]GTGGCCAGAGGTGCT	2186
rs773546896	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67938761	AAGACTAGTCTGGCC[A/G]CATTTTTTAAAATTG	2186
rs773572080	snp	A/G	1.65603e-05	0.00287747	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912850	GAGCAGAGCAAAACC[A/G]TGGTCACCACGACAG	2186
rs773578597	snp	C/T	1.64806e-05	0.00287054	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67893480	TCAAGAAGGGAAGTA[C/T]CGCGTCTACCACAAT	2186
rs773624795	in-del	-/A			intron-variant	BPTF	GRCh38.p7	17:67938128	GTACAGTCAGAAATT[-/A]TTACATTTTTGAATT	2186
rs773658822	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67923389	TCATTTATTCAGTGC[A/G]GTAAAGTCCTAGCTT	2186
rs773672342	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67945021	GTACCAAAATACAAA[A/T]TTCTCAACTTTATTT	2186
rs773772936	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67896204	CCTGACCTTGTGATC[C/T]GCCCGCCTTGGCCTC	2186
rs773782137	snp	C/T	0.0336038	0.125191	intron-variant	BPTF	GRCh38.p7	17:67929322	TTTTAATTATGGCTT[C/T]ATCTTTTTTTAAGGC	2186
rs773808108	snp	A/C	3.33189e-05	0.00408146	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67893637	CATGGGTCCAAAGTT[A/C]TTACCATATCTACTC	2186
rs773844687	snp	A/G	3.48979e-05	0.00417705	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67909596	GCCAAAAATAATATG[A/G]ATGAAAATATGGATG	2186
rs773860490	snp	A/G	1.6782e-05	0.00289668	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67909752	AAGATTACTGAGAAG[A/G]AGGACCAAGGTAAGG	2186
rs773901238	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67909002	ACCACACCCAGATAA[A/T]TTTTGTATTTTTAGT	2186
rs773906752	snp	A/T	0.00012815	0.00800366	intron-variant	BPTF	GRCh38.p7	17:67874781	CTATTTGGTTATATA[A/T]AGGAATAATTTTTTT	2186
rs773909598	snp	C/T	1.66579e-05	0.00288595	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912587	ATGAAAATGGTCTGC[C/T]CATCAACAAAAATGA	2186
rs773926002	snp	A/G	0.000115736	0.00760622	missense, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67891925	CATCTGGCTCAACTC[A/G]AATCATCACCAGATT	2186
rs773931445	snp	C/T	1.65345e-05	0.00287524	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911932	TGTGAGGACAGGCTG[C/T]CGGTCAAGGGGACTG	2186
rs773960660	snp	C/T	8.27274e-05	0.00643093	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911401	GATGATGTCTCCATT[C/T]GGAGCCCAGAAACAA	2186
rs773960907	in-del	-/G			intron-variant	BPTF	GRCh38.p7	17:67883021	AAAAAAAAAAAAAAA[-/G]AAAAGAAAAAAGGGC	2186
rs773964244	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67843217	ATGTAGATGTATGTA[C/G]ATATATACCTATATA	2186
rs773969343	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67869893	TGTAGTCCCAGCTAC[G/T]CGGCAGCCTGAGGCA	2186
rs773973295	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67941999	AATCCAGATAGATCA[A/G]TAGGAAAAAAGACAA	2186
rs773975793	snp	C/G	1.64933e-05	0.00287165	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67928392	CGACAGTGATTGCAA[C/G]TTCCACTACTTCCCC	2186
rs773984672	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67920360	AAGCACAGCAAAGGG[C/T]TATAATAATACCTCT	2186
rs774000097	snp	A/C			upstream-variant-2KB	BPTF	GRCh38.p7	17:67824481	CTCTCAATAAATATT[A/C]ATATGTTTATAACAC	2186
rs774020182	snp	A/G	1.6476e-05	0.00287014	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67928493	ACAACTGGAACCAAA[A/G]TGGTACTAACTACTA	2186
rs774044403	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67932035	GTATTTATCCATCCA[G/T]CATTATCATTTTACA	2186
rs774050070	snp	C/T	9.57368e-05	0.00691804	intron-variant	BPTF	GRCh38.p7	17:67891807	ATAATTATTTACTTA[C/T]TGTCAGCAATTGCTT	2186
rs774063713	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67972709	ATATATACTCACCTA[C/T]GTGTTCTCCTAGTAC	2186
rs774088986	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67843724	GGTCTTTTGTGATAA[A/T]GAGATTTTTAAATTG	2186
rs774103297	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67907768	AATATGTATCTCTAC[A/G]TAGACATTTTTCCAT	2186
rs774125118	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67862922	TTCAAGGCAGCTTAG[G/T]TTTTTTCTATCAAGC	2186
rs774134546	snp	A/C/G			intron-variant	BPTF	GRCh38.p7	17:67964772	TTGGGAGGCCAAGGT[A/C/G]GGCGGATCACAAGGT	2186
rs774149298	snp	C/T	1.64781e-05	0.00287033	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67866636	GACATAACTGAAGAC[C/T]TGACCAATAAGGCTC	2186
rs774149344	snp	A/G	0.000188697	0.00971148	upstream-variant-2KB	BPTF	GRCh38.p7	17:67825495	CTGCGGCCGCTGTCG[A/G]TTCCCCCAGTCACCG	2186
rs774168286	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67861113	CTACTCTTCATCCAG[C/T]GTTCTCATCTTAGTA	2186
rs774171230	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67833992	ATTTCTCTTTTCCTT[A/T]TTCACTCCTTATTTC	2186
rs774214008	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67915904	ATGAGCAGACTTACC[A/G]TGCATGTGGTGTGTT	2186
rs774221704	in-del	-/GAAAAT	1.6859e-05	0.00290331	cds-indel, nc-transcript-variant	BPTF	GRCh38.p7	17:67866477	AGAGAAGAAGATACA[-/GAAAAT]GAAAATGAAAAGAAA	2186
rs774234393	snp	C/T	3.32939e-05	0.00407993	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67912327	TGAAAGAAACAGCTC[C/T]GAAACAAAATCGCAT	2186
rs774251387	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67871894	GCAGTGGCATGATCT[C/T]GGCTCACTGCAACCT	2186
rs774298745	snp	C/T	1.65468e-05	0.00287631	intron-variant	BPTF	GRCh38.p7	17:67932041	ATCCATCCAGCATTA[C/T]CATTTTACATCTCAA	2186
rs774304323	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67884197	GGCTGTAGTGCAGTG[G/T]CGCAATCTCAGCTCA	2186
rs774339828	snp	G/T	1.65647e-05	0.00287786	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911518	AAAACAAAAGGAAAT[G/T]ATTTTTTCATCGATG	2186
rs774356543	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67847406	GTAATTCCAGCTACT[C/T]GGGAGGCTGAGGCAG	2186
rs774380222	in-del	-/A			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67888206	TTTCACCCACAACTT[-/A]AAACTTTTTCAAAAA	2186
rs774426848	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67878563	GGTATCATCAGCATC[A/C]CTCTTTGTCTTTTTG	2186
rs774449323	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67857322	CCCGCCACCGTGCCC[A/G]GTTAATTTTTTGTAT	2186
rs774479300	snp	A/C	1.66032e-05	0.0028812	intron-variant	BPTF	GRCh38.p7	17:67894217	GGACTCCCTTTTGAA[A/C]TACTAGCCTATTAAT	2186
rs774482754	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67838185	AAGTAAACAAATGAG[C/T]ATGGCTGCTTTCTAA	2186
rs774484752	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67916870	TTTTTATTTTATAGC[C/G]TTTGTCTACACCATA	2186
rs774492090	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67939795	TCAGGCAGGAGAATC[A/G]CTTGAACCCAGGAGG	2186
rs774502631	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67886369	TTTTTCTTTTTTTTC[-/T]TTTTTTTGTGTGTGT	2186
rs774515614	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67865367	TATTTAACATTTATT[A/G]ATCACTGGTGTGCCC	2186
rs774526204	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67904026	TAGTCTTTGTATTTT[A/T]TTTATTTATTTATTT	2186
rs774532922	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67977710	TTAGCTGGGCGTGGT[A/G]GCACATGCCTGTAAT	2186
rs774536616	snp	A/T	1.64844e-05	0.00287087	missense, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67886190	ACCTCCATCCAGCCT[A/T]ATCTGGAAAACAGTA	2186
rs774551463	snp	A/T	1.65712e-05	0.00287843	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911109	GTTTACACTGGAAGA[A/T]AAACAGCGACTCGAA	2186
rs774555784	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67856192	CTCTTTGGGGTATTT[G/T]TATGTGTTCAGTTTT	2186
rs774570197	in-del	-/G			upstream-variant-2KB	BPTF	GRCh38.p7	17:67825033	CTGCCCGGTGCCCTC[-/G]GGTCGCTTGGGCCGC	2186
rs774586985	snp	A/G	1.65441e-05	0.00287607	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67874909	AAGAATGAGACTGAG[A/G]ATGACTCTAAAGATG	2186
rs774589699	snp	A/T	1.6473e-05	0.00286988	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67854487	GTCTGAAGGGGTGAT[A/T]CAGTATGATGACCAT	2186
rs774604319	snp	C/T	1.64765e-05	0.00287019	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67893507	CAATCAATACTCCAC[C/T]AATTCATTTGCTTTG	2186
rs774627665	snp	A/G	3.30775e-05	0.00406665	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67912399	CCTTGAGACCCTGCC[A/G]TCAACCAAAGAGTCT	2186
rs774632253	snp	A/C	3.58423e-05	0.00423319	intron-variant	BPTF	GRCh38.p7	17:67931867	CCATTATACTTTAAT[A/C]TTTTTAAAGCATTTT	2186
rs774633556	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67875246	TCTCTATTTATACTT[C/T]CCATTAAGTTGCCAT	2186
rs774641899	snp	A/C	1.65644e-05	0.00287783	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67929457	TAGGCCCAATACCTC[A/C]GGCTCTGGAGGAACC	2186
rs774646008	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67840897	GTAAGAGTTCTTTAT[A/G]TATTTTGGATATAAG	2186
rs774655665	snp	A/T	1.66849e-05	0.00288828	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67893661	TCTACTCTGAGACTG[A/T]CTATCACCCAATTAG	2186
rs774737736	snp	A/G			synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67911184	TACAAATTCTTCAAA[A/G]AATCTCTCTGAATCA	2186
rs774761656	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67951567	TAGTTGTAGTTTATA[A/T]CCTTTATGTATAAAA	2186
rs774768255	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67829482	TGCCCCCCACCCCCC[A/G]GATGTGACATTTTGA	2186
rs774770973	snp	A/G			missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912298	AATGGTGATGTCATC[A/G]TGGAAGATTTTAATG	2186
rs774783160	snp	A/C	3.34007e-05	0.00408647	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67826323	GGAGCCATAGTACCT[A/C]CAGCAGCACTCCAGG	2186
rs774807020	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67851406	ACCATTGTTTGTGTG[C/T]ACGTTCAATTGAGTT	2186
rs774868449	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67909460	TGTCTTTTTTTTTTT[C/T]TTAAATGAAAAAATG	2186
rs774914041	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67827773	GTCCTAACATAACTG[A/T]AAAAAGGTAATTTCT	2186
rs774916814	snp	A/G	1.65127e-05	0.00287334	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67913018	TCCTATAGAAAATTT[A/G]TTACCAAGAGCAGCA	2186
rs774946500	snp	C/G	1.70656e-05	0.00292104	intron-variant	BPTF	GRCh38.p7	17:67866723	TTTTATTTTTGTTAA[C/G]TCTGAGCTAAACCGT	2186
rs774948398	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67920331	CACACATCGATGCCT[A/T]TAAGCCTTGTTCTAA	2186
rs774965654	snp	A/C	1.80902e-05	0.00300745	intron-variant	BPTF	GRCh38.p7	17:67913202	GGTATGTACTTTAAA[A/C]TGTATTTGGGGGAGG	2186
rs774998175	snp	C/G			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67898232	CCAGGCATGGTGTTG[C/G]ATGCCTTTAGTCCCA	2186
rs775006643	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67830123	TATACTGAGAAGGAT[C/T]GTATAGGAAGTGTTT	2186
rs775019975	snp	A/G	1.65364e-05	0.0028754	synonymous-codon, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67891950	CAGATTGCGGAATCC[A/G]GATAGCAAACTTAGT	2186
rs775036000	snp	C/T	1.64811e-05	0.00287059	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67928535	CCAGCTACAGTAACA[C/T]TCCAACAAAACAAGA	2186
rs775051108	snp	C/T	3.29582e-05	0.00405931	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67866651	CTGACCAATAAGGCT[C/T]GGGGCAGTAACAAAT	2186
rs775079599	snp	C/T	5.36322e-05	0.00517815	intron-variant	BPTF	GRCh38.p7	17:67903763	TTTTCCAAGTTAACA[C/T]TGTCTTTCTATGCAT	2186
rs775087944	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67885283	ACTATTAAATTGTCC[A/T]CAGAAGTTAGCAATC	2186
rs775088968	snp	A/G	1.66521e-05	0.00288544	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67912696	AAAAACTGTGATCAA[A/G]GTAGAAAAAGGCGAT	2186
rs775094744	snp	A/C			missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67909590	TTTTTAGCCAAAAAT[A/C]ATATGGATGAAAATA	2186
rs775096703	snp	C/G	2.47418e-05	0.00351714	intron-variant	BPTF	GRCh38.p7	17:67910849	TCAGAGTAAAAATTA[C/G]ATTTATATAAATGTC	2186
rs775114991	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67867609	CATCATGTTTTCCTC[G/T]GGGTTGTCGGTTTCT	2186
rs775186000	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67916984	AGGACATGATATTTA[A/G]TGCAGTTAAGTAAAT	2186
rs775207545	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67872106	GCTGGGATTACAGGC[A/G]TGAGCCACTGCGCCC	2186
rs775223816	snp	C/G	1.77332e-05	0.00297763	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67826084	CGCGGCCCGGAGGGC[C/G]GTCAACAAAGTGGTG	2186
rs775235302	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67857925	CCCAAGTAGCTGGGA[C/T]TACAGGCATGCGCCA	2186
rs775248375	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67933535	GCTCATGCTACTGCA[C/T]TCCAGCCTGGGAGAC	2186
rs775256199	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67834209	GTTTTAGTTTCCAAA[C/T]ATTTGGGAATTTTTT	2186
rs775272925	snp	G/T	2.11965e-05	0.00325543	intron-variant	BPTF	GRCh38.p7	17:67893345	ATTGACATAAATAAT[G/T]CAGTCTTTTTATTTT	2186
rs775299001	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67926745	TATTTCTTTGCCTCC[-/T]TTTTTTTTTAGAGAT	2186
rs775309549	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67869228	TCTAAAAGGCAATGT[A/G]AGATAGGATTTTATA	2186
rs775319249	snp	C/T	1.73228e-05	0.00294297	intron-variant	BPTF	GRCh38.p7	17:67922820	ATATTGCTTAAAATA[C/T]TCTGATTTCCTTTCC	2186
rs775325709	snp	A/G	1.65457e-05	0.00287621	intron-variant	BPTF	GRCh38.p7	17:67904848	AGAAGGAAGTAAGTA[A/G]TTAAAATTACATGTC	2186
rs775341722	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67904180	ATTATAGGCGTGCAC[C/T]ACCACGCCTGGCTAA	2186
rs775362278	snp	A/G	3.3432e-05	0.00408838	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67911211	ATCACCAGTAATAAC[A/G]AAAGCAAAAGAAGGG	2186
rs775405613	in-del	-/AGT	1.74668e-05	0.00295518	splice-acceptor-variant, intron-variant	BPTF	GRCh38.p7	17:67891842	GCCTATTCATTTGAC[-/AGT]AGGTGATTTCAAATC	2186
rs775436710	snp	A/G/T			intron-variant	BPTF	GRCh38.p7	17:67872848	ACGCCTGTAACCCCA[A/G/T]TGCTTTGGTAGGCCA	2186
rs775445627	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67917967	CAGGCACCCACCACC[A/G]CGCCTGGCTAATTTT	2186
rs775482419	snp	A/G	1.64969e-05	0.00287196	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67903900	ATGGGTAAAATACAC[A/G]TTTCCAGTTAAGCAT	2186
rs775483608	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67835496	CTGAGTGAAGTCCTC[C/G]TTTGTGGAGACTCTG	2186
rs775513770	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67927483	TATAATAGAAGAAGT[C/G]TAGAAAAACTTTTAT	2186
rs775535922	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67830336	CTGGTGTTACCCTGG[A/G]AGAGTTAGTGATTTA	2186
rs775544984	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67958730	AGCACTTTGGGAGGC[C/T]GAGGCGGGTGGATCA	2186
rs775552532	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67866777	TGAAAATAGATTAAA[A/G]TTTTCAAGTACAGTC	2186
rs775606901	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67860717	TATAATTACGTGAAC[A/G]CAGCATTATATTTCA	2186
rs775616568	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67859584	TTTAGAATGTGTTTT[A/G]TAAGAATATTTTCAA	2186
rs775617267	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67939874	GACAGAGCGAGACTC[C/T]GTCTCAAAAAAAAGA	2186
rs775620456	snp	A/G/T	4.69928e-05	0.00484712	intron-variant	BPTF	GRCh38.p7	17:67875781	TGCCTCTGTAATGGG[A/G/T]GGAATCCTTCCCTTT	2186
rs775636852	in-del	-/AGTAAG	3.31483e-05	0.004071	cds-indel, nc-transcript-variant	BPTF	GRCh38.p7	17:67911494	AGAGGCCAGGAACCC[-/AGTAAG]AGTAAAACAAAAGGA	2186
rs775655356	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67892475	AGCAGAGTACTGTGG[A/T]TAGGACAGCATGGCA	2186
rs775719215	snp	A/T	1.648e-05	0.0028705	missense	BPTF	GRCh38.p7	17:67931998	AAGGCAATTATTCGA[A/T]CACCTGTGATGGTAC	2186
rs775741535	snp	C/G	1.6531e-05	0.00287493	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67874953	AGAAGAATTTGAAGA[C/G]CAGTCCCTTGAAAAA	2186
rs775756482	snp	C/T	1.67055e-05	0.00289006	intron-variant	BPTF	GRCh38.p7	17:67931893	ATTTTAATTCATTGT[C/T]CTTTGTGTCATTTAT	2186
rs775778419	snp	A/C	1.86834e-05	0.00305636	intron-variant	BPTF	GRCh38.p7	17:67875072	TAGTGTTATTTATGA[A/C]ATCTCCAGTTTTACT	2186
rs775779038	snp	G/T	1.65367e-05	0.00287543	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67911364	TACCACAAACAAACT[G/T]TATCCAAAAGATCGA	2186
rs775783593	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67851739	CCTGAATTTCTCTCT[A/G]AAGTTGTGATACCAG	2186
rs775786478	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67913987	GTCCTTGCTTTCTCC[G/T]TTTTCATGTCCTTGT	2186
rs775786669	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67900378	CCAAAGTGCTGGGAT[A/T]ACAGGCGTTAGCCAC	2186
rs775799040	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67829417	ATAGGTATACGTGTG[C/T]CATGGTGGCTTGCTG	2186
rs775811681	snp	G/T	1.85324e-05	0.00304399	intron-variant	BPTF	GRCh38.p7	17:67913214	AAAATGTATTTGGGG[G/T]AGGGAGAAAATTTTA	2186
rs775833597	snp	C/T	8.68093e-05	0.00658765	intron-variant	BPTF	GRCh38.p7	17:67853925	TTTGTAATGATGTCA[C/T]GTCTTTATCTACAGG	2186
rs775834046	snp	A/G	1.65012e-05	0.00287234	intron-variant	BPTF	GRCh38.p7	17:67894025	TCTCTCATTTCTTCT[A/G]AAATACAGGGCAAAT	2186
rs775835286	snp	A/G	1.65531e-05	0.00287686	missense, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67875610	CAAATCTTGGCGACA[A/G]CACAACAAATGCAAC	2186
rs775839576	snp	A/G	1.66538e-05	0.00288559	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67912654	CACAGAAGTCACCAC[A/G]ATGACCTCCACAGTG	2186
rs775854212	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67977295	CAAGGTGGGTGGATC[A/G]CTTGAGGTCAGCAGT	2186
rs775888037	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67879610	TTATTTAAAAAAAGA[C/G]ATTTCTTTGGCTATG	2186
rs775890504	in-del	-/A			intron-variant	BPTF	GRCh38.p7	17:67869828	CTCTACTAAAAATAC[-/A]AAAAAAAAAAAAAAA	2186
rs775892911	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67872368	TAAATGGCACTGGGA[A/C]AGTAGGGAGGATGTA	2186
rs775942045	in-del	-/ATATTTTGTCAGTCTTTAGTATCAG			intron-variant	BPTF	GRCh38.p7	17:67879044	TCTTTAGTATCAGGA[-/ATATTTTGTCAGTCTTTAGTATCAG]GAATATTTTGGCCTC	2186
rs775960250	in-del	-/TTGG			intron-variant	BPTF	GRCh38.p7	17:67898676	TTTTTTTTTTTTTTT[-/TTGG]GAAGATGTATTGCAA	2186
rs775965733	in-del	-/TTT			intron-variant	BPTF	GRCh38.p7	17:67908492	GTTGTCACTGACCAC[-/TTT]TTTTTTTTTTTTTTT	2186
rs775976716	snp	C/G	1.64822e-05	0.00287068	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67928410	CCACTACTTCCCCAA[C/G]AAGCAGTACAACCAG	2186
rs776001323	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67848337	ATTTTTTTAGTTGCT[A/G]CAATAACTAAAACAT	2186
rs776030664	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67933801	CAGTGGCTCATGCCT[A/G]TAATCCCAGCACTCC	2186
rs776031487	snp	C/T	3.29462e-05	0.00405857	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67854086	ATTTACGAGGTACTG[C/T]GGAACTTTGGCACTG	2186
rs776067730	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67850051	TCTCACTGTAGTCCT[A/G]TATTTACTTACGTAG	2186
rs776083797	in-del	-/TTGA	1.65244e-05	0.00287436	intron-variant	BPTF	GRCh38.p7	17:67893327	ATGAAATTCACATCT[-/TTGA]TTGACATAAATAATG	2186
rs776087253	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67951453	AACAGAAGCACTTTG[G/T]CCTCTTGAACAAGCC	2186
rs776087488	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67853137	GTAGGTGATTAAATG[A/G]GATAGATACGTTTGT	2186
rs776105655	snp	C/T			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67886964	CTTAACGTATATCTT[C/T]GTGTACTTGTGCAGG	2186
rs776118501	snp	A/G	1.65195e-05	0.00287393	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912929	CTGTGAGCAAAGAGT[A/G]TTCCACACGAGACAA	2186
rs776133417	snp	G/T	1.65353e-05	0.00287531	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911941	AGGCTGCCGGTCAAG[G/T]GGACTGAAGCAAATG	2186
rs776182744	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67865240	AAGGGAACTCCACCC[A/G]TATCCTTTTATTTAT	2186
rs776184785	snp	C/G	1.69178e-05	0.00290837	intron-variant	BPTF	GRCh38.p7	17:67909769	GGACCAAGGTAAGGA[C/G]AGTCAGCTGTGGAGG	2186
rs776194230	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67865975	ATATTATAAAGTTAG[C/T]TGGGTATCGTGGCAC	2186
rs776204760	snp	A/G	1.66735e-05	0.00288729	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67826208	GATTCTGAGGACGAC[A/G]AGGAGGATGAGATGG	2186
rs776209888	snp	G/T	3.6513e-05	0.00427261	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67826126	CGAGAGCGAGGAGGA[G/T]GAGGAAGAGGAGGAC	2186
rs776228112	snp	A/G/T	0.000115352	0.00759366	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67866653	GACCAATAAGGCTCG[A/G/T]GGCAGTAACAAATCC	2186
rs776237286	snp	A/G	1.64988e-05	0.00287213	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911598	CAAAAAACCGCTCAT[A/G]CAGGAGGAAAGTGAC	2186
rs776241307	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67967204	TGGAGTGTACTAGCG[C/T]GATCTCACATCACTA	2186
rs776242441	snp	C/T	3.29913e-05	0.00406135	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67893460	AACAATTATTTTAAA[C/T]TGGGTCAAGAAGGGA	2186
rs776265069	snp	C/T	1.65836e-05	0.0028795	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67912819	AGGCGGCAGTGTGGA[C/T]ATCATCTCTGTAAAG	2186
rs776290520	snp	A/G	1.65045e-05	0.00287263	intron-variant	BPTF	GRCh38.p7	17:67903934	GTAATTTTTACAACA[A/G]CCCTTTAAAATAGTG	2186
rs776330869	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67873083	GAGACTCTGTCTCTA[A/G]AAAAGTAAAAAATAA	2186
rs776352191	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67940169	ATTATCATTTTGGTT[G/T]TAGATTTATAGGAAG	2186
rs776368365	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67905570	AAAAATTAGCCAGGT[A/G]TAGTGCCACATGGCT	2186
rs776406832	snp	A/G			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67886648	GATCTTTCTGCAGTT[A/G]CATTTATGTATGTAT	2186
rs776423692	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67857686	TACTCAGGCTGATCT[C/T]GAACTTGTGAGCTCG	2186
rs776459413	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67859949	GTACCTGTGGGTGAT[C/T]TTTTGATACATTGTC	2186
rs776459728	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67885571	CTCCAGCCTGCGCAA[C/G]AGAGTGAGACTCCAT	2186
rs776479409	snp	C/T	1.65553e-05	0.00287705	stop-gained, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67886304	ACACCTGTCTCTATT[C/T]AGGAAGAGATAGGTA	2186
rs776481554	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67840814	GCAATCCGCCTGTCT[C/T]GGCCTCCCAAAGTGC	2186
rs776493066	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67910331	ACATTCATGCAGAAG[-/T]TTTTTTGTGGCCATG	2186
rs776509678	snp	C/T	4.94181e-05	0.00497057	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67894086	CCCAGAGAATTTGCA[C/T]TGGCTTTAGCCATTT	2186
rs776516529	in-del	-/AGT	1.67097e-05	0.00289043	cds-indel, nc-transcript-variant	BPTF	GRCh38.p7	17:67912174	AATTTCTGAGAGTAG[-/AGT]AGTAAGTGGTAATGT	2186
rs776521834	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67844786	TTCACTCTTGTTGCC[C/T]AGGCTGGAGTGCAAT	2186
rs776541248	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67919379	GTCTCTTCAAAACTC[-/T]TAATTTAAAAAGAAA	2186
rs776544784	snp	C/T	0.000377287	0.0137296	upstream-variant-2KB	BPTF	GRCh38.p7	17:67825489	CTGGGCCTGCGGCCG[C/T]TGTCGGTTCCCCCAG	2186
rs776548348	in-del	-/A			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67888589	ACGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA	2186
rs776598623	snp	C/T	1.66131e-05	0.00288206	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912338	GCTCCGAAACAAAAT[C/T]GCATTTGCTGAGTTC	2186
rs776622837	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67894554	AGGCTGGTCTTGAAC[C/T]CCTGACCTTGTGATC	2186
rs776623153	snp	G/T	3.29641e-05	0.00405968	missense, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67886212	AAAACAGTAACAGCA[G/T]CAGTGAACTAAATTC	2186
rs776623543	snp	C/T	1.65806e-05	0.00287924	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67922846	TTTCCAAAGAAACGC[C/T]TACACCTCAGAGGAA	2186
rs776634540	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67881606	CCTCCCAGGTTCAAG[C/T]GATTCTCCTGCCTTA	2186
rs776678129	snp	C/T	3.31235e-05	0.00406948	intron-variant	BPTF	GRCh38.p7	17:67924529	GTTTCTGATAAGTTT[C/T]TCCTTTTTTTCCTGC	2186
rs776680416	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67980327	TCCAGCCTGGGCAAC[A/G]CTGAGGCTCCATCTC	2186
rs776729465	snp	A/G	1.65353e-05	0.00287531	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912407	CCCTGCCATCAACCA[A/G]AGAGTCTGACAGTAC	2186
rs776731152	snp	A/G	3.34454e-05	0.0040892	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67866497	TGAAAATGAAAAGAA[A/G]ATTTGGTATTACAGC	2186
rs776735755	in-del	-/GTAA			intron-variant	BPTF	GRCh38.p7	17:67939405	GTTAGTAATGAGTCT[-/GTAA]GTGTCAAATTAGCTA	2186
rs776745252	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67882161	TTTTAGCAGAATAAA[A/G]TGTTTGAGGCTTATG	2186
rs776752523	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67830448	GTCACTGGTTTGACA[A/G]TATTATTCCTATCAG	2186
rs776754499	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67927832	CCTTCATAGATAGGT[A/G]CCTTGGAGGAATTAA	2186
rs776758938	snp	C/T	1.64942e-05	0.00287173	missense	BPTF	GRCh38.p7	17:67932016	CCTGTGATGGTACAG[C/T]CAGGTATTTATCCAT	2186
rs776771759	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67914309	ATTTATTAATACAAC[C/G]AGTCATAGTTTGTTT	2186
rs776813911	snp	C/T	4.94246e-05	0.0049709	missense, nc-transcript-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67918815	CGGCCAAGGCTCCTC[C/T]AGGAGGAGGGACTAC	2186
rs776821346	in-del	-/AAAC			intron-variant	BPTF	GRCh38.p7	17:67855315	CAAAAATAAATAAAT[-/AAAC]AAAAAGTTTCTAGGT	2186
rs776841092	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67831430	ATATGATTTGTGAGT[A/G]GTAGAGAGGTGTGTC	2186
rs776871749	snp	C/T	6.59141e-05	0.00574045	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67920074	AGAGATGTTGGTCCT[C/T]ATGGCATTCGATCTG	2186
rs776885249	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67929272	TTCTCCTCAGCAACC[A/G]AGCACCACGTAATGC	2186
rs776898713	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67927601	TATTACAGTGAAACA[G/T]AAACCTTTCACAGCT	2186
rs776900081	snp	C/T	3.3077e-05	0.00406662	intron-variant	BPTF	GRCh38.p7	17:67894205	ATGATGAGTATTGGA[C/T]TCCCTTTTGAAATAC	2186
rs776907807	in-del	-/A			intron-variant	BPTF	GRCh38.p7	17:67921210	TTGAGAATCCGTGTC[-/A]AAAAAAAAAAAAAAA	2186
rs776911756	snp	A/G			utr-variant-3-prime	BPTF	GRCh38.p7	17:67982762	ATAAAATCCAGCCCC[A/G]GTTACATATAATCAT	2186
rs776930911	snp	A/G			intron-variant, utr-variant-5-prime	BPTF	GRCh38.p7	17:67888775	CTGTGTTTGAGAGGT[A/G]AGAAACATATAAGAA	2186
rs776939279	snp	A/C	1.64732e-05	0.0028699	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67854098	CTGCGGAACTTTGGC[A/C]CTGTTTTGAGATTAT	2186
rs776943617	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67938618	GAATAATTGGCTTAT[A/G]GTTTGGGGGGAAAAT	2186
rs776946779	snp	A/G	1.66424e-05	0.0028846	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67911988	GCAGAAGAAATTAGA[A/G]GAGAGACCAGTTAAT	2186
rs776959241	snp	C/G	1.65414e-05	0.00287583	missense, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67875622	ACAACACAACAAATG[C/G]AACTTCAGAAGAGAC	2186
rs776966327	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67840320	TTATGTTGCCCAGAC[G/T]GATTTCAAACTCCTG	2186
rs776968738	snp	A/G/T			intron-variant	BPTF	GRCh38.p7	17:67868687	CATTATCTGCTATAC[A/G/T]TATAATCCTATTAAT	2186
rs776974854	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67853227	TGGACATCACATCTC[A/C]TAATTGGAGAACAGG	2186
rs776980701	snp	A/G	9.90998e-05	0.00703847	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67928561	CAAGAACTTTCATCA[A/G]ACCTTTGCTACATGG	2186
rs776982102	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67902059	TGCCACTGGCACACC[C/T]ACCAGCATGCTACTC	2186
rs776992330	snp	C/T	1.6473e-05	0.00286988	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67854274	AGATAGCGTTAATTC[C/T]ACACTGTATTTCATA	2186
rs777000270	snp	A/G	1.70618e-05	0.00292072	intron-variant	BPTF	GRCh38.p7	17:67909781	GGAGAGTCAGCTGTG[A/G]AGGGCAGCCTGGGGG	2186
rs777003231	snp	A/G	2.20437e-05	0.00331984	intron-variant	BPTF	GRCh38.p7	17:67910856	AAAAATTACATTTAT[A/G]TAAATGTCTTTGTTT	2186
rs777022119	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67867879	CTCCACATCCTCCCC[C/T]AACCCCTCAAACCCC	2186
rs777047568	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67896302	TATTTCATGATGGAC[A/T]GTTACATAGCAGTGA	2186
rs777063027	in-del	-/AT			intron-variant	BPTF	GRCh38.p7	17:67869363	AAAGTCAAAACAGGA[-/AT]GGGTAATCAAGTGTT	2186
rs777081996	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67937832	TCCTAAGATGAGATC[C/T]GGCCGGGTACAGTGG	2186
rs777097205	snp	A/C	1.65647e-05	0.00287786	intron-variant	BPTF	GRCh38.p7	17:67893998	ATTTAAGGTCAACCT[A/C]GTGAAATAATTTCTC	2186
rs777162730	snp	A/G	1.66032e-05	0.0028812	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67875006	ATGATGACCCTGAGC[A/G]AGGAAAATCTGAGGG	2186
rs777175923	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67975005	GTCTTTCCGGTGACC[A/G]GCCCCAATCCTGAAG	2186
rs777205898	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67855169	AGCCAGGTGTGGTGG[C/T]GCACACCTGTAATCC	2186
rs777210854	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67839407	AAGATGATCATATAG[G/T]TTTTCTCCTGCAAGC	2186
rs777216405	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67921655	GATTAAATTAACTTG[A/G]GAGTTCTTCTTGGAG	2186
rs777234275	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67937189	GGCCGGGCGCGATAG[C/T]TCACGCCTAATATAC	2186
rs777235008	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67875754	TGCCAGGTACAGAGG[A/G]CAGCGTATCAATGCC	2186
rs777256966	in-del	-/AT			intron-variant	BPTF	GRCh38.p7	17:67946779	AAAGTTTTTGAAAAC[-/AT]ATTATTTCATAGCTT	2186
rs777268997	snp	C/T			intron-variant, utr-variant-5-prime	BPTF	GRCh38.p7	17:67889200	AATATGGCCTTTGGG[C/T]AGAGGGTGTTCAGTA	2186
rs777280132	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67901636	TTTGCAGAAAAATAA[A/G]TATGAAAGGCCAGTA	2186
rs777325912	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67902567	CTTATGAGAGACTAC[A/G]AAGAGCCTATGGAGA	2186
rs777328873	snp	C/T	5.82926e-05	0.00539842	intron-variant	BPTF	GRCh38.p7	17:67893357	AATGCAGTCTTTTTA[C/T]TTTTTTGGTCAGGTA	2186
rs777339293	snp	C/T	1.6476e-05	0.00287014	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67894138	TTGTGATGCTACCAA[C/T]ATGGCGAGAATCTTT	2186
rs777357982	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67951257	CCTGAGAATCAGCCC[C/T]AATCCTGAGGCTCTC	2186
rs777364129	snp	A/G	1.64784e-05	0.00287035	synonymous-codon	BPTF	GRCh38.p7	17:67931967	TAGAACACCACTCCA[A/G]CAGTCAACACTAGGA	2186
rs777364482	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67855707	ACATCCTGTAGATAT[A/G]TGGTCAGAGGGATGG	2186
rs777380197	in-del	-/GAGGAG	0.000295703	0.0121558	cds-indel, nc-transcript-variant	BPTF	GRCh38.p7	17:67826151	GAGGACATGGTCTCC[-/GAGGAG]GAGGAGGAGGAGGAC	2186
rs777389676	snp	A/G	1.67119e-05	0.00289062	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912059	AAAAGAATAATGAAA[A/G]TCGAGAGTCTGAAAA	2186
rs777426505	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67921157	GGAGGTTGCAGTGAG[C/T]TGAGATCACACCACT	2186
rs777528502	snp	C/G	1.65108e-05	0.00287317	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911909	TTTCTGGTGAGTCCA[C/G]TGGAAACTGTGAGGA	2186
rs777534607	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67850753	ATTCTATCCAATGAA[-/T]TAAGCCACAATTTGA	2186
rs777541612	in-del	-/TAAC			intron-variant	BPTF	GRCh38.p7	17:67853259	ATCTAAAAAGTTGTT[-/TAAC]TGACTGTTAAGAAAT	2186
rs777542460	snp	C/T	3.29522e-05	0.00405894	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67928472	GCCCCCATAAGTGGC[C/T]CAGTTACAACTGGAA	2186
rs777549695	snp	C/G	1.65463e-05	0.00287626	missense, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67891913	CTGGAAAAGGAGCAT[C/G]TGGCTCAACTCGAAT	2186
rs777566006	snp	A/G	3.29468e-05	0.00405861	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67918762	AGTGAGCCTGATGTT[A/G]CGGTTACTGTGGGCA	2186
rs777594874	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67839899	CATTCTTACCTGCAA[A/G]TGTATGAAGAGTTCC	2186
rs777598607	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67953176	CCATGTTAGCCAGGA[C/T]GGTCTCGATCTCCTG	2186
rs777622545	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67827162	GGGAAATGCAGTTTC[G/T]TGTCACCTGTTGCAG	2186
rs777652424	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67883975	CACACAAAAGTAAGC[A/G]TATTATAAGTATTGT	2186
rs777676450	snp	A/G			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67897117	CAGTCACCTGAGGTC[A/G]GGAATTCGAGACCAG	2186
rs777692636	snp	A/G	1.64735e-05	0.00286993	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67854019	CCTTGAATTTCCCAA[A/G]TCCTCTGAGGATTTA	2186
rs777699656	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67943315	ATGTATATGGAGCTT[A/G]CTTAGTACATGGACT	2186
rs777704833	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67938371	AAAGACCTTGGCCAC[A/T]CTATGTTATGCTGTC	2186
rs777746307	snp	A/T	9.40654e-05	0.00685739	intron-variant	BPTF	GRCh38.p7	17:67892050	GTGTGTTCTTTCTGT[A/T]TAAAACAAAAATCTG	2186
rs777750649	in-del	-/AAT			intron-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67919173	GAGACTCTGTCTCAA[-/AAT]AATAATAATAATAAT	2186
rs777795424	snp	A/G	1.67284e-05	0.00289205	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67874834	GAAATTTTGGAATCC[A/G]TAAGAGCCAAAAAGG	2186
rs777812926	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67864129	AAAACCAAATATACA[G/T]ACATAATGTATATTT	2186
rs777817589	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67842640	TTTTGATGACAAAGG[C/T]TGTGGTCCACAATGA	2186
rs777850325	snp	A/C	1.65455e-05	0.00287619	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67826259	GATTATCCGGAGGAG[A/C]TGGAAGACGACGACG	2186
rs777864369	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67862505	CCAAGATCACACAAC[G/T]ACAAAGTGGTGGGAT	2186
rs777868760	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67970402	ACCTTGTCCCACAAA[C/T]GTAATAATAAAATAC	2186
rs777877355	snp	C/T	1.65663e-05	0.002878	intron-variant	BPTF	GRCh38.p7	17:67923011	GAAATGGTTAATACC[C/T]GGTCAGCTATTTGAA	2186
rs777895508	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67906105	TTTGTTTTTTTGAAA[C/T]GGAGTCTTGCTCTGT	2186
rs777916215	in-del	-/A			intron-variant	BPTF	GRCh38.p7	17:67843984	GGTCAGGCTGGTCTC[-/A]AAACTCCTGACCTCA	2186
rs777943282	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67904982	ACTAGTTTAGTTTAC[C/T]AAAACCCTAAAACTT	2186
rs777972120	snp	A/G	1.6473e-05	0.00286988	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67854413	GAGAACAAGATCAAA[A/G]TTCTACAGTTTCTAG	2186
rs777997890	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67884883	GTGTAATTTTCCCTT[C/T]GTGTATTGTGAGACT	2186
rs778011356	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67843472	CAGCCTCTCAAAGTG[C/T]TGGGATTATAGGCGT	2186
rs778012138	snp	C/G	3.29728e-05	0.00406021	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67904798	TTTGTTCCTAAATTG[C/G]CAGGCAATACTAATG	2186
rs778026959	in-del	-/T	0	0	intron-variant	BPTF	GRCh38.p7	17:67886359	AAGGGAAGTTTTTTC[-/T]TTTTTTTTCTTTTTT	2186
rs778060171	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67873315	ATACAAAAATTAGCC[A/G]GGTGTGGTGGCAGGC	2186
rs778083886	in-del	-/TTC			intron-variant	BPTF	GRCh38.p7	17:67883706	CCTGGGTTCAAGCAG[-/TTC]TTCTGCCTCAGCCTC	2186
rs778092271	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67916658	GTAATCCCGGCTACT[C/T]GGGAGGCTGAGGCAG	2186
rs778113061	in-del	-/T	1.68091e-05	0.00289901	intron-variant	BPTF	GRCh38.p7	17:67904882	CATAATCGTTTCTGC[-/T]TTATATTTCTTATAA	2186
rs778130370	snp	C/T	1.80188e-05	0.00300151	intron-variant	BPTF	GRCh38.p7	17:67928317	TGTTTTTATTTAGAA[C/T]TATTTTGATTCATGT	2186
rs778176775	snp	A/G	1.65353e-05	0.00287531	missense, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67891943	TCATCACCAGATTGC[A/G]GAATCCAGATAGCAA	2186
rs778196151	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67908491	GTTGTCACTGACCAC[-/T]TTTTTTTTTTTTTTT	2186
rs778200660	snp	A/G	1.65004e-05	0.00287227	missense, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67886163	GAGAGCAGTAACACT[A/G]GTGCTACCACTACCT	2186
rs778206300	snp	A/G	1.99027e-05	0.00315451	intron-variant	BPTF	GRCh38.p7	17:67909547	TGCTAATACTCTGGA[A/G]ATAACGTAAATTATC	2186
rs778226418	snp	C/T	1.64768e-05	0.00287021	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67854666	TGACTGACTGTGTTG[C/T]TGAAATCCAAAAAAA	2186
rs778235841	snp	A/G	1.65883e-05	0.00287991	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912484	AATCAGGTAGAAGAT[A/G]TGGAAATAGAAACCT	2186
rs778237783	snp	C/G	1.67125e-05	0.00289067	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67911190	TTCTTCAAAAAATCT[C/G]TCTGAATCACCAGTA	2186
rs778258853	snp	A/G	1.65669e-05	0.00287805	missense, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67875607	CAGCAAATCTTGGCG[A/G]CAACACAACAAATGC	2186
rs778279959	in-del	-/GTGATACGAGTCA			intron-variant	BPTF	GRCh38.p7	17:67885875	GTACTGGAGACTAAG[-/GTGATACGAGTCA]GTGAGTTAGAGTTGG	2186
rs778311725	snp	C/G	1.64732e-05	0.0028699	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67854064	GCATATAATGAATGT[C/G]ATTGCCATTTACGAG	2186
rs778333565	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67903391	CTTAAAAAAATCTGT[A/G]TATTTTGATAAGGAA	2186
rs778377698	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67906014	TGTCACAAACCTGCA[C/T]GTTGTGCGCACGTAC	2186
rs778390822	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67899016	CAAGATATAGACACA[A/G]TTATTATATGCAGTT	2186
rs778407810	snp	A/C/G			intron-variant	BPTF	GRCh38.p7	17:67878145	TACTGGAACCATACA[A/C/G]TATATACTCTTTGAT	2186
rs778428287	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67909406	TTAGGTCAGCCAGGC[A/C]TATAGGATTATATGG	2186
rs778429129	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67841600	AAAGATGGGGTTTTG[C/T]CATGTTGCCTAGGCT	2186
rs778438321	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67856677	CTAGAGGAGCAATGG[C/T]ATGGAAGGGCCTTTT	2186
rs778442179	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67930493	CCTGAGCCACTGCAC[C/T]TGGCCCAGATATGTA	2186
rs778474279	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67859551	TGTGGCTCTTAGGAG[A/G]TAGAACCTGGAATTT	2186
rs778489211	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67827561	GGTTTTAAAAGCCTT[G/T]AAAAAATAAAGTTTA	2186
rs778560968	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67850174	CTTGTAATAAATGTT[C/T]ATTTAATAGCTTATT	2186
rs778561197	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67915903	AATGAGCAGACTTAC[C/G]GTGCATGTGGTGTGT	2186
rs778563606	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67847285	TTTGGGAAGCCGAGG[C/T]GGGTGGATCACCTGA	2186
rs778573431	snp	A/G	1.65274e-05	0.00287462	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67893430	AAAAAGGAAGTGATC[A/G]TGAAAGGAAATATCA	2186
rs778617869	snp	A/G	1.76278e-05	0.00296877	intron-variant	BPTF	GRCh38.p7	17:67928645	ACTTTGGTTCAGGAA[A/G]AAGAATTTTCAACCC	2186
rs778656399	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67939348	TGGAAAAAAGGCAGC[A/G]AGTAAATATTAAAAG	2186
rs778665693	snp	C/T	0.000204801	0.0101172	intron-variant	BPTF	GRCh38.p7	17:67910831	ATATATAAATTCCTC[C/T]TTTCAGAGTAAAAAT	2186
rs778690633	snp	C/T	1.64727e-05	0.00286986	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67854209	CTTTTGAAAGCAGTT[C/T]TGCGTGAAGAAGACA	2186
rs778695024	snp	A/G	1.66774e-05	0.00288763	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912088	AAGAAAGGACAGAGA[A/G]CAAGTACATTTCAAA	2186
rs778700040	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67899134	GGGACAAGAGGAACA[A/G]CAGAAAATACACCAC	2186
rs778708037	snp	A/G					GRCh38.p7	17:67838669	TTTTTTAGTAGAGAC[A/G]AGGTTTCACCAGCCC	2186
rs778708162	snp	A/C	1.66294e-05	0.00288347			GRCh38.p7	17:67912777	AACCACCACTACAAC[A/C]GTGACCAAGCTTTCC	2186
rs778709267	snp	A/T					GRCh38.p7	17:67924451	AGATAATATCATACC[A/T]TTGTATGATGTGAAA	2186
rs778715157	snp	A/G					GRCh38.p7	17:67910671	CAGGCATGGTGGCAC[A/G]TGCCTATAATCCCAG	2186
rs778722088	snp	C/T					GRCh38.p7	17:67828895	TGAAATTATTAACTC[C/T]TTAGAGATAAGTATT	2186
rs778731562	snp	A/G	2.12583e-05	0.00326017			GRCh38.p7	17:67892079	TGTGGAATGTGAGAT[A/G]ATTTTAATTACCACA	2186
rs778734131	snp	A/G					GRCh38.p7	17:67976525	ACCATGTCTCTACAA[A/G]AATTTAAAAAATTAA	2186
rs778763746	snp	C/T	1.65141e-05	0.00287346	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911570	ATGATATTGGTACTT[C/T]GATCTGTAAGAACAA	2186
rs778801730	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67884979	GTTTGAATTGGGCAT[A/T]TTTCCATATGCCTAA	2186
rs778812848	in-del	-/AAG			intron-variant	BPTF	GRCh38.p7	17:67842906	GTAAAATAAATATAA[-/AAG]AAGGTCTTTAGGCCA	2186
rs778828817	in-del	-/AA	2.55542e-05	0.00357442	intron-variant	BPTF	GRCh38.p7	17:67910847	TTCAGAGTAAAAATT[-/AA]ACATTTATATAAATG	2186
rs778851101	snp	C/G			intron-variant, utr-variant-5-prime	BPTF	GRCh38.p7	17:67889128	GCAGAGGCTGATGTA[C/G]ATCTGTAGCCTGCTG	2186
rs778853451	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67934336	TAGCCTGGCCAACAT[C/G]GTGAAACCCCTTCTC	2186
rs778875705	snp	A/G	4.98807e-05	0.00499378	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67909676	GCCTGATTCTGAAAA[A/G]GATGAGGTAAAAGGT	2186
rs778892012	snp	A/G/T	3.40334e-05	0.00412502	intron-variant	BPTF	GRCh38.p7	17:67866721	CATTTTATTTTTGTT[A/G/T]AGTCTGAGCTAAACC	2186
rs778908779	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67836135	AGATGTTAGTATGTC[C/T]TAGTGTGTCTGGGTT	2186
rs778943775	snp	A/T			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67898026	AATTGGCTTCACCTT[A/T]GACACCAATCTCCAA	2186
rs778954297	snp	A/G	3.30721e-05	0.00406632	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912892	CTGACCACCACGGGA[A/G]GCACACTGGTTACAT	2186
rs778957423	snp	A/C			missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67866646	AAGACCTGACCAATA[A/C]GGCTCGGGGCAGTAA	2186
rs778996553	snp	C/G/T	5.31019e-05	0.00515253	intron-variant	BPTF	GRCh38.p7	17:67928328	AGAACTATTTTGATT[C/G/T]ATGTTTCCTCTCCTT	2186
rs779005752	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67865758	AGTTAGTGACCATCT[C/G]TGTTGAAGTCTTTAA	2186
rs779015268	snp	C/T	1.92996e-05	0.00310635	intron-variant	BPTF	GRCh38.p7	17:67909562	AATAACGTAAATTAT[C/T]GTTACATGGTTCTTT	2186
rs779050102	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67837197	AAAAAAACTAGTCCT[A/G]TTGAGAATTCAGGCT	2186
rs779051957	snp	A/G	3.32231e-05	0.00407559	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912511	ACCTCAGAAGTTAAG[A/G]AAGTTACTTCATCAC	2186
rs779058124	snp	C/T	1.67251e-05	0.00289176	synonymous-codon, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67891872	ATCGGAGAAGTCCAA[C/T]GGGGAGCTAAGTGAA	2186
rs779083171	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67935651	ACCTGAGGTCAGGAG[G/T]TCAAGACCCGCCTGC	2186
rs779094993	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67935727	TGGGAATGTTGACAG[A/T]TGCCTATAATCCCAG	2186
rs779129008	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67873668	ACAGATAAGCAAGTG[A/G]GCAATGGTAAATGAA	2186
rs779165514	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67859333	TTATTTTTTATTTTG[A/T]AGAGGTCTCACTGTG	2186
rs779204945	snp	C/T	1.65384e-05	0.00287557	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911351	GTGATCCTAGTCATA[C/T]CACAAACAAACTTTA	2186
rs779255460	in-del	-/ATTGAGTATTTCAGTTA	3.34806e-05	0.00409136	intron-variant	BPTF	GRCh38.p7	17:67919985	GTATTTCAGTTGGTT[-/ATTGAGTATTTCAGTTA]ATTAATACTATTGAA	2186
rs779258428	snp	A/T	1.65345e-05	0.00287524	intron-variant	BPTF	GRCh38.p7	17:67894014	GTGAAATAATTTCTC[A/T]CATTTCTTCTGAAAT	2186
rs779258634	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67867312	TTTTAAGAAATAATA[A/T]TCTTTTTGAACTTTT	2186
rs779260084	snp	A/G	1.65674e-05	0.00287809	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911444	AAAATTCCATTGAAA[A/G]TGACATAGAAGAAAA	2186
rs779267257	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67906062	ATTTAAAAAAATAAT[A/G]AGGTTTTTTTTGGGG	2186
rs779293346	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67845108	TGCTGTATAAGTGCA[C/T]GTCTCCTCCTCAGCA	2186
rs779294504	snp	A/G	3.33267e-05	0.00408194	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67912627	TGGAGAATCTAAAAG[A/G]AAAACCGTCATCACA	2186
rs779304526	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67880530	CATGTTCCCTTTATC[A/G]TTTAGTTTAAAATAT	2186
rs779332775	snp	C/T	1.6522e-05	0.00287414	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67854709	TCGACATGAACCTAT[C/T]GGATATGATAGAAGT	2186
rs779357294	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67893312	AAGACAGTTGATTAG[A/G]TGAAATTCACATCTT	2186
rs779385840	snp	C/T	3.43271e-05	0.00414275	intron-variant	BPTF	GRCh38.p7	17:67866417	GAACTGTCAGATAAG[C/T]GGCATTATGTCTAAC	2186
rs779393279	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67931014	GCTCACACCTGTAAT[C/T]CCAGCACTTTGGGAA	2186
rs779415645	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67907867	CCATATTCCACTTGC[C/T]CTGGTTGTCTTAGAG	2186
rs779421442	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67957036	GCCTGTAATCCTAGC[A/C]CTTTGGGAGGCTGAG	2186
rs779442405	snp	C/T	3.29598e-05	0.00405941	missense	BPTF	GRCh38.p7	17:67931993	TAGGAAAGGCAATTA[C/T]TCGAACACCTGTGAT	2186
rs779444907	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67881789	TGCAGGTGTGAGCCA[C/T]CCACCTGGCCCAGAA	2186
rs779459852	snp	A/G	1.64925e-05	0.00287158	intron-variant	BPTF	GRCh38.p7	17:67894170	GGACATACCAGGTAA[A/G]TGAATTCTGAGCCTT	2186
rs779470937	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67905981	GTGCAGCACACCAAC[A/G]TGGCACATGTATACA	2186
rs779474054	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67923580	CTCTGCCTCCTGGGC[C/T]CAAGCAATTCTGCCT	2186
rs779491277	snp	C/G	0.000209622	0.0102356	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	BPTF	GRCh38.p7	17:67825571	GGGGCCCCAGCAATT[C/G]GGATTGAGCCTTCTC	2186
rs779506952	snp	A/T	1.65825e-05	0.00287941	missense, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67886136	TTTCTAGAAGAACCT[A/T]ACAAGACATGTGAGA	2186
rs779507288	snp	C/T	1.64727e-05	0.00286986	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67854250	TACCTTTGGACCTGC[C/T]GATCTGAAAGATAGC	2186
rs779514491	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67829749	AAGAGGAATTTACCT[C/T]ATTGGTAATTTAGAG	2186
rs779523506	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67831708	AGTAGTATTCTGGGT[A/G]ACACAGGAGCAAATC	2186
rs779526856	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67926945	TTTTTAACTGATTTA[A/G]TCAGATGATGTCTCT	2186
rs779537438	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67865898	ATTATTTGAGATAAC[G/T]CCTTCAAAAACCAGA	2186
rs779580447	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67960130	CTGTTGCTCCTTTGC[-/T]TTCTCTTCTTCCCTC	2186
rs779587422	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67895162	AGCACCTAGGGAGAC[C/G]GAGGTACTAAAAACA	2186
rs779606120	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67939449	ATTCTTAGCAACTGT[C/T]CTACATGGGGGAAAA	2186
rs779610122	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67829049	TACAGTGGGTGTCAT[A/T]ATCTCTAAATACTTT	2186
rs779611691	snp	A/G			missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67854038	TCTGAGGATTTAATG[A/G]TGCCTAATGAGCATA	2186
rs779646270	snp	A/T	1.80817e-05	0.00300675	intron-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67929495	ATTCACAAGTAAGAA[A/T]TCTTACAGACTTATT	2186
rs779646516	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67880022	TATTTTCTGTTGTTT[C/T]CTTAGGTTCATTTTC	2186
rs779658350	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67947900	ACTTGTTTATCTTGA[C/T]TGAAGTTCATTAAAT	2186
rs779703595	snp	G/T	1.64762e-05	0.00287016	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67929388	TCCATCAAGTACAGG[G/T]ACCAGTCAGCAAACC	2186
rs779723761	snp	A/G	1.66454e-05	0.00288486	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67874848	CATAAGAGCCAAAAA[A/G]GGAGACATTGATAAT	2186
rs779724381	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67835529	CCCAGCATTATTTGT[C/G]TATGTGATGGTATTG	2186
rs779792016	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67871438	AGAGTGAGACTTTGT[C/T]TCCAAAAAAAAAAAA	2186
rs779832062	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67844070	TGCCCGGCCCCCGCC[-/T]TTTTTTTTTTTTTTT	2186
rs779840035	snp	C/G	1.64806e-05	0.00287054	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911681	CCAATGACAGAGATG[C/G]CACACCTCTGTCAAG	2186
rs779841424	snp	A/C	1.65002e-05	0.00287225	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67910988	GTCAGGAGAGTTCTC[A/C]AGTAGATGTGGTCAA	2186
rs779854134	snp	A/G	3.432e-05	0.00414232	intron-variant	BPTF	GRCh38.p7	17:67866727	ATTTTTGTTAAGTCT[A/G]AGCTAAACCGTTGGT	2186
rs779918027	snp	G/T	1.68007e-05	0.00289828	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67826268	GAGGAGATGGAAGAC[G/T]ACGACGACGACGCCA	2186
rs779933352	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67899471	TTTTCCTGGGAACCT[C/T]CTTTGATAGTAACAA	2186
rs779949331	snp	A/T	1.65696e-05	0.00287828	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67893586	CATAAGTTCTGTCTG[A/T]CTCCAGCAGGAGAGT	2186
rs779952355	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67867084	CCTGGTGGACCGAAA[C/G]ATTGTGCAGTGCATG	2186
rs780010111	snp	A/G	1.74943e-05	0.00295751	synonymous-codon, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67892025	TAAATTATTTAAGGA[A/G]GGCAAAGAGGTGTGT	2186
rs780062771	snp	C/T			synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67874980	AAAAGACAGTGACGA[C/T]AAAACACCAGATGAT	2186
rs780067827	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67835663	CCACAGTCCTGGTAA[-/T]TTTTTTTTTTTTTTT	2186
rs780072498	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67886534	GTTTTTGTTTTCAAA[A/G]TCTACAAAAGCACAC	2186
rs780073818	in-del	-/T			intron-variant, utr-variant-5-prime	BPTF	GRCh38.p7	17:67888914	TTGGCAGGTTTGGGG[-/T]TTTTTTCTGACAGTA	2186
rs780141003	snp	A/G	1.65693e-05	0.00287826	missense, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67891897	AGTGAATCTCCTGGA[A/G]CTGGAAAAGGAGCAT	2186
rs780189160	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67846606	AGGCACTTGTTATTT[C/T]TCAAATTCCCTTTCA	2186
rs780193896	snp	A/G	1.65707e-05	0.00287838	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911455	GAAAATGACATAGAA[A/G]AAAAAGTCTCTGACC	2186
rs780196215	snp	C/T	1.71009e-05	0.00292406	intron-variant	BPTF	GRCh38.p7	17:67866436	ATTATGTCTAACATA[C/T]AAAGTATTTCCCCCC	2186
rs780213844	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67845243	TTGAAAGTAGTATTT[A/G]TCTGTAAGGTGATTC	2186
rs780227340	snp	A/G	1.64768e-05	0.00287021	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67928463	GTTATGGTGGCCCCC[A/G]TAAGTGGCTCAGTTA	2186
rs780227412	snp	C/T	1.66183e-05	0.00288251	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67912519	AGTTAAGAAAGTTAC[C/T]TCATCACCTATTACT	2186
rs780244853	snp	A/G	1.65113e-05	0.00287322	intron-variant	BPTF	GRCh38.p7	17:67894189	ATTCTGAGCCTTGTA[A/G]ATGATGAGTATTGGA	2186
rs780266668	snp	C/T			upstream-variant-2KB	BPTF	GRCh38.p7	17:67823875	GTGCAGTGGTGCGAT[C/T]TCGGCTCACTGCAAC	2186
rs780297427	in-del	-/T	0	0	intron-variant	BPTF	GRCh38.p7	17:67924532	CTGATAAGTTTCTCC[-/T]TTTTTTTCCTGCAGA	2186
rs780396205	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67854850	GAGCTATGCTGTTGA[G/T]GTGGTATAAACCTTT	2186
rs780427193	snp	A/G/T	3.3046e-05	0.00406474	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911549	ACTCTAAACTAGCCA[A/G/T]TGCAGATGATATTGG	2186
rs780447521	snp	A/G	6.66378e-05	0.00577187	intron-variant	BPTF	GRCh38.p7	17:67920187	ATTAACCTGTTAACC[A/G]TGTATTTTATGAATT	2186
rs780448462	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67846740	GACAGGGTCCCTGTC[G/T]CCTAGGGTGGAGTGC	2186
rs780452773	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67931592	GAGCTTACAGAAAGT[A/G]CGACTCCACATTTTC	2186
rs780457873	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67902506	ATGGAATTTGAGTAC[A/G]TTAGCTCCCAGTGAG	2186
rs780460026	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67929208	ACTGATTTCAGTCCT[C/T]GGATCTCACATTCTA	2186
rs780461173	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67893886	GTACTTCTAACTTAC[A/T]GAACCGACACCACTA	2186
rs780473362	snp	A/G	9.98619e-05	0.00706548	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912748	ACAGAAAATTGTGCA[A/G]AATCCACTGTCACAA	2186
rs780482446	snp	A/G	1.76241e-05	0.00296846	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67903836	AAAAGGAGAAAGTCA[A/G]AAAAAAAGAGAAGAA	2186
rs780487984	in-del	-/GAG	0.00103332	0.0227066	cds-indel, nc-transcript-variant	BPTF	GRCh38.p7	17:67826208	GATTCTGAGGACGAC[-/GAG]GAGGATGAGATGGAA	2186
rs780540951	snp	C/T	0.000171718	0.00926442	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	BPTF	GRCh38.p7	17:67825607	ACCCGCTTCCGTCGG[C/T]CGGGCCCCTCCCGCC	2186
rs780555087	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67939041	TGAAATAGGCACACA[C/G]AGCTGGCAGTAGTGT	2186
rs780560651	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67979270	TAATGACATTGGGCC[A/G]GGCACGGTGGTTTAC	2186
rs780576593	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67871495	ATATATTCATCGTAT[A/G]GATCTGTACTTTATA	2186
rs780593661	snp	A/G	1.73132e-05	0.00294216	missense, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67875723	AAGAAGGTGGCATCT[A/G]AGCTCCCCCAGGATG	2186
rs780605303	snp	A/G	1.65056e-05	0.00287272	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67920023	ACCATAGAAACATCC[A/G]AAACTGAAATCACAA	2186
rs780616933	snp	C/T			missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67928464	TTATGGTGGCCCCCA[C/T]AAGTGGCTCAGTTAC	2186
rs780638119	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67877097	ATATATCATACCAGA[G/T]TTTAAAGAGGAGTTT	2186
rs780665908	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67852710	TGAATTAAATATTTT[G/T]TACTTAAATGAATGT	2186
rs780718291	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67981075	GAGGTAGGAGGATCA[C/T]CTGAGCCCTGGAGGT	2186
rs780728745	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67883509	TTTGACTTTCATTCC[C/T]TCTCTCTCTAGGTAA	2186
rs780756922	in-del	-/AT			intron-variant	BPTF	GRCh38.p7	17:67933638	TATGAATTAAGTAAC[-/AT]GTCATATTAAAGTGT	2186
rs780815291	in-del	-/T	1.65496e-05	0.00287655	intron-variant	BPTF	GRCh38.p7	17:67929326	AATTATGGCTTCATC[-/T]TTTTTTAAGGCGTTG	2186
rs780833185	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67919453	GGCTGGGGCCAGGAG[G/T]ATTGCTTGAGCCAGG	2186
rs780833285	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67830924	TGCACAAACATGAAA[A/C]AGAACCATATCAAAT	2186
rs780838833	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67867176	TCCACTGTAAATTAG[A/G]GATGCTATACATTTT	2186
rs780840247	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67853616	ATTATTATTATTATT[A/G]TTTCCTTAGAGATCC	2186
rs780868762	snp	C/T	1.93377e-05	0.00310942	intron-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67929514	TACAGACTTATTTGG[C/T]TTGATGTGTTGAGCA	2186
rs780874239	snp	A/C	0.000208746	0.0102142	intron-variant	BPTF	GRCh38.p7	17:67826389	CACCTCCTCTGCCCT[A/C]CCCCCTTGCTCACTC	2186
rs780894841	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67837882	TCCCAAATGGCAGGA[C/T]GTCTGTTTTGAGAGT	2186
rs780920137	snp	A/C	1.69493e-05	0.00291108	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67913151	TGGATATATGGCCAT[A/C]TCCTTCTCCTAGACC	2186
rs780977991	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67901361	TCAATAAGAAAGCAT[G/T]AATTAATTTATGTTT	2186
rs781007882	snp	A/C	1.65578e-05	0.00287726	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67826278	AAGACGACGACGACG[A/C]CGCCAGTTACTGCAC	2186
rs781036442	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67838913	TTCTAGTTGAAAACT[A/G]ATGAATTTTAAAAAT	2186
rs781047955	snp	C/T	1.66125e-05	0.00288201	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67874856	CCAAAAAGGGAGACA[C/T]TGATAATGTTAAAAG	2186
rs781058120	snp	C/T	3.73197e-05	0.00431954	intron-variant	BPTF	GRCh38.p7	17:67893764	ATTGCTGTAAATATA[C/T]TAAATGTTTATAAAA	2186
rs781061313	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67920793	GTCTACTTAGAAAAT[C/T]CATGAGAATTAAAAG	2186
rs781082621	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67844559	CTAATTTTTTTTTTC[-/T]TTTTTTTTTTTTTGT	2186
rs781098116	snp	A/G	1.86336e-05	0.00305229	intron-variant	BPTF	GRCh38.p7	17:67909571	AATTATCGTTACATG[A/G]TTCTTTTTAGCCAAA	2186
rs781118428	snp	C/T	1.6489e-05	0.00287128	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67853981	CCTCGTTCTCCTATA[C/T]TGGAAGAAAAAGACA	2186
rs781122595	in-del	-/AAAG			intron-variant	BPTF	GRCh38.p7	17:67872711	TTCTGTCTCAAAAAA[-/AAAG]AAAGAAAGAAAGAAA	2186
rs781125705	snp	C/T			missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911282	CAAATAATGATCAAC[C/T]TGAGGACTTGATTCA	2186
rs781149476	snp	A/G	1.65299e-05	0.00287483	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67909705	GTTCAGATGCTGCAA[A/G]AGGAGCAGACCAAAA	2186
rs781160057	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67826969	TTCTTCGAGTGCTAA[G/T]GGGCCCGTGCAACAG	2186
rs781190797	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67908301	GTAGCTGGGACTACA[G/T]GCTCGTACCACCATG	2186
rs781204245	snp	C/T	1.7626e-05	0.00296861	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67826174	GGAGGAGGAGGACGG[C/T]GACGCCGAGGAGACC	2186
rs781213921	snp	A/G			upstream-variant-2KB	BPTF	GRCh38.p7	17:67823913	TCCCAGGCTCAAGCG[A/G]TTCTTCTGCCTCAGC	2186
rs781214973	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67875314	AGAGTATACACTTTT[A/G]TATGTGATAAAATGT	2186
rs781217545	snp	A/G	1.64784e-05	0.00287035	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67866618	GAAATCCACCGACAC[A/G]TGGACATAACTGAAG	2186
rs781220842	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67974330	TGTGCTCTCACGCTA[C/T]GGTCAACGTGGGAGA	2186
rs781272795	snp	A/G	1.66507e-05	0.00288532	intron-variant	BPTF	GRCh38.p7	17:67866697	CTAATGGTGAGAGGG[A/G]CATTTTCTCATTTTA	2186
rs781289077	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67961204	ACTTCTTTGAAATAC[C/G]TACATTGCATAAAAT	2186
rs781303362	snp	C/T			intron-variant, utr-variant-5-prime	BPTF	GRCh38.p7	17:67889114	TTAAACAGTGAGCTG[C/T]AGAGGCTGATGTAGA	2186
rs781307918	in-del	-/AT			intron-variant	BPTF	GRCh38.p7	17:67913296	GATAAGACAGGAAAC[-/AT]ATTAATGGCCAAAGA	2186
rs781311223	snp	C/T	1.73878e-05	0.00294849	intron-variant	BPTF	GRCh38.p7	17:67928336	TTTGATTCATGTTTC[C/T]TCTCCTTCACTTTTT	2186
rs781339001	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67849096	CATGAGTTTCCAAAA[C/G]CCTTTCTGCTTGGTA	2186
rs781356407	snp	A/G	3.32823e-05	0.00407922	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912754	AATTGTGCAAAATCC[A/G]CTGTCACAACCACCA	2186
rs781358774	snp	C/T	9.77445e-05	0.00699019	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67826059	GCGGCGGCCACCTGG[C/T]CCGGACCACCGCGGC	2186
rs781379283	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67908272	GAAGCAATTCTCCTG[C/T]TTCAGTCTCCCAAGT	2186
rs781412272	snp	A/C			intron-variant, utr-variant-5-prime	BPTF	GRCh38.p7	17:67888669	ACAATCCATGAGCCA[A/C]ATTATGAATTTAACT	2186
rs781461878	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67916635	GCTGGATGTTTGGGC[A/G]GGCGCCTGTAATCCC	2186
rs781481887	snp	C/T	1.80348e-05	0.00300284	intron-variant	BPTF	GRCh38.p7	17:67922794	CCAGAAGTACTTTAA[C/T]TTTAGAAGCAATATT	2186
rs781482415	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67867943	AACAGCCACACTTAG[C/T]GGGTGAGGAGTTATG	2186
rs781486673	in-del	-/AAAT			intron-variant	BPTF	GRCh38.p7	17:67907717	TCCTGCAGTGTTTTA[-/AAAT]AAATCCCAGAAATCA	2186
rs781492353	in-del	-/TTTTTTCTT	1.8851e-05	0.00307004	intron-variant	BPTF	GRCh38.p7	17:67886352	TCCTTTAAAGGGAAG[-/TTTTTTCTT]TTTTTTCTTTTTTTT	2186
rs781506318	snp	A/G			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67897044	TCAAGAATAAAAAAA[A/G]AGGCCGGGCATGGTG	2186
rs781509613	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67931415	GAGTGAGCCAGGCTA[C/T]GATGAGCTGTGATTG	2186
rs781553532	in-del	-/GACGAC	3.33378e-05	0.00408262	cds-indel, nc-transcript-variant	BPTF	GRCh38.p7	17:67826265	CCGGAGGAGATGGAA[-/GACGAC]GACGACGACGCCAGT	2186
rs781554427	snp	A/G/T	0.00011562	0.0076025	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911558	TAGCCAGTGCAGATG[A/G/T]TATTGGTACTTTGAT	2186
rs781602924	snp	A/G/T	3.31023e-05	0.0040682	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912383	GTAACTACCGAGATA[A/G/T]CCTTGAGACCCTGCC	2186
rs781603564	snp	A/G	1.64841e-05	0.00287085	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911632	ATTGTTTCTTCTTCC[A/G]AGAGTGCTTTACATT	2186
rs781606307	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67931000	GGCCGGATGCGGTGG[C/T]TCACACCTGTAATCC	2186
rs781622130	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67874192	TCTGTACACTGTGGT[C/T]CTTCTGTATCCCGTG	2186
rs781630841	snp	A/G/T	3.30296e-05	0.00406373	missense, intron-variant, nc-transcript-variant	BPTF	GRCh38.p7	17:67886155	AGACATGTGAGAGCA[A/G/T]TAACACTAGTGCTAC	2186
rs781648487	snp	A/G	3.34336e-05	0.00408848	intron-variant	BPTF	GRCh38.p7	17:67904685	TTGTTTAATCAAAAT[A/G]TTTTCATTTACACCA	2186
rs781656083	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67890547	CCTGGGACAGTCACT[A/G]TGGCCAGCTAGTGGT	2186
rs781663583	snp	C/T	1.64844e-05	0.00287087	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67922962	GAAGAAGAACTGGAA[C/T]TGTGGGAGATCAGGG	2186
rs781689906	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67932902	GCAGAATAAAATTCA[A/G]TGTTTAATAAAAAGG	2186
rs781713591	snp	G/T	1.69789e-05	0.00291362	intron-variant	BPTF	GRCh38.p7	17:67904670	GCATTGTTATTCTTA[G/T]TGTTTAATCAAAATG	2186
rs781715602	snp	C/T	1.64727e-05	0.00286986	synonymous-codon, nc-transcript-variant	BPTF	GRCh38.p7	17:67854382	AGAGGCAGAGGACTA[C/T]CCATATGGACCAGTA	2186
rs781722613	snp	C/T	1.67357e-05	0.00289268	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67912275	AATCTGCTATAAGGC[C/T]ATTCATTAATGGTGA	2186
rs781747425	snp	A/G	4.95184e-05	0.00497562	missense, nc-transcript-variant	BPTF	GRCh38.p7	17:67911026	GAGGGTTTTCATCTA[A/G]GGACTAGTTACAAAA	2186
rs781747989	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67857222	GTGCGAGTGCAATGG[C/T]GTGATCTCGGCTTAC	2186
rs781768846	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67872579	GGTGTGGTGGTATGC[A/G]CCTATAGTCTCAGCT	2186
rs781785846	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67980000	TCGCACCACTACACT[C/T]TAGCCTGGGCAACAA	2186
rs781785941	snp	C/T	3.39253e-05	0.00411844	intron-variant	BPTF	GRCh38.p7	17:67964178	ACATCATCCCATGTG[C/T]TTTGAACTCACATTT	2186
rs781786043	snp	C/T	3.30131e-05	0.00406269	synonymous-codon	BPTF	GRCh38.p7	17:67940509	AGTCTCCGCCCCTAA[C/T]ACGGTTTCCTCAACA	2186
rs781790358	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67947866	TTTATCGTGCACACG[C/T]ACAGAGTTCTGAGTT	2186
rs781791946	in-del	-/T	1.85451e-05	0.00304503	intron-variant	BPTF	GRCh38.p7	17:67959910	CTCTAGTTTTTTGTC[-/T]TGAAAGTTTAGCTAT	2186
rs781793376	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67968512	GGTCAGGTGCGGTGG[C/T]TCACGCCTGTAATAC	2186
rs781794768	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67975385	CCACTAGTACAGAGA[-/T]TTTTGTTCTTAATTC	2186
rs781794996	snp	A/G	0.000116049	0.00761649	missense	BPTF	GRCh38.p7	17:67945449	ACTGTCACCCCAGAT[A/G]CAGGTACATCAAGAC	2186
rs781798708	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67966909	GATCGAGACTATCCT[A/G]GCCAACATGGTGAAA	2186
rs781798738	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67954851	AGGAAGAAGTTCAGT[C/T]TCTCTCTATAAATAG	2186
rs781799870	snp	A/G	1.98695e-05	0.00315188	missense	BPTF	GRCh38.p7	17:67948305	TGCAAATTGAAGTGC[A/G]GGTAAGAGGGCACAT	2186
rs781802035	snp	C/T	0.000362337	0.013455	synonymous-codon	BPTF	GRCh38.p7	17:67944245	GACTGTACTCCCAGG[C/T]CCAGGCCAGCAGCTA	2186
rs781803358	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67971758	GCAGTGAGCCAAGAT[C/G]GTTGCGTTGCAGTGA	2186
rs781804052	snp	A/G	1.64741e-05	0.00286998	intron-variant, missense	BPTF	GRCh38.p7	17:67946060	CTCAGATCCAGTCAC[A/G]GGTTGTGGCTCAGAT	2186
rs781808827	snp	A/G	4.94197e-05	0.00497066	synonymous-codon	BPTF	GRCh38.p7	17:67945740	TCCTGTTCGTGTCCA[A/G]AGTCCATCACAGACT	2186
rs781809972	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67952865	TTCCTCCTCTTTCCC[C/T]CTGTGCTAGTCTTTT	2186
rs781811526	snp	A/G	1.84008e-05	0.00303316	missense	BPTF	GRCh38.p7	17:67959571	GACCTGAAAATTAAG[A/G]AAGAAAAAGACCTGA	2186
rs781813250	snp	A/C	3.29636e-05	0.00405964	intron-variant, missense	BPTF	GRCh38.p7	17:67946194	ACAGTGCAGGCAGCC[A/C]GTGTGCAAGAGCAGT	2186
rs781814289	snp	A/G	0.000399973	0.014136	intron-variant, missense	BPTF	GRCh38.p7	17:67963457	CGGGCACAAGAGGGC[A/G]GCAGTGAGGAATTGT	2186
rs781816141	snp	A/G/T	3.29496e-05	0.00405881	missense	BPTF	GRCh38.p7	17:67945718	AAAGTAATGTCCAAG[A/G/T]ACAGTCTCCTGTTCG	2186
rs781817345	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67946708	AGTTTGCATGTAGAC[G/T]ATGCAAATTATAGAC	2186
rs781819732	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67951056	TCAAGTAATCCACCC[A/G]CCTTAGTCTCCCAAA	2186
rs781820068	in-del	-/A			utr-variant-3-prime, downstream-variant-500B	BPTF	GRCh38.p7	17:67983636	CCTTTCAGTGTTCTT[-/A]ACACGTTGTATCACT	2186
rs781824417	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67949113	GTTCATGCCCATAAT[C/T]CCAACACTTTGGGAA	2186
rs781827412	snp	C/G	0.000115814	0.0076088	missense	BPTF	GRCh38.p7	17:67945874	AGATACCTTCCCAAG[C/G]CCAGCCACAGTCACA	2186
rs781828267	snp	A/G	1.84667e-05	0.00303859	missense	BPTF	GRCh38.p7	17:67959544	AATTGATAACAGGAA[A/G]AGCTGAAGAGAGACC	2186
rs781830044	in-del	-/ATTAA			intron-variant	BPTF	GRCh38.p7	17:67940063	ATGAATTAATTTTTT[-/ATTAA]ATTAAATTAGCACTT	2186
rs781833781	snp	A/G	1.70702e-05	0.00292144	intron-variant	BPTF	GRCh38.p7	17:67944411	ATGTCGGATGTTACT[A/G]CTACACGTGGCTGGG	2186
rs781834293	snp	A/G	1.64743e-05	0.00287	missense	BPTF	GRCh38.p7	17:67964333	CAGTCAACAGAGGAT[A/G]CCATGACAGTGCTCA	2186
rs781834982	snp	C/T	1.64746e-05	0.00287002	intron-variant, stop-gained	BPTF	GRCh38.p7	17:67946083	GCTCAGATACAGGCT[C/T]AGCAAAGTGGTGTGC	2186
rs781835110	snp	C/T	1.65048e-05	0.00287265	intron-variant	BPTF	GRCh38.p7	17:67966540	GAATTAGTGTTTTCA[C/T]TGACAATAATGATGC	2186
rs781835693	snp	G/T	3.31439e-05	0.00407073	missense	BPTF	GRCh38.p7	17:67948100	ATTGTCTGTAACCAG[G/T]TGATGAAGTATATTT	2186
rs781837183	snp	C/G	1.69309e-05	0.0029095	missense	BPTF	GRCh38.p7	17:67959652	CCAGCTCCTCCAGCC[C/G]CTCCAGCCCCTCCAC	2186
rs781839379	snp	C/T	2.30987e-05	0.00339835	intron-variant	BPTF	GRCh38.p7	17:67948328	GGGCACATCCTTTTC[C/T]TCTGTGTCCAGTGTT	2186
rs781841253	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67976781	ATTCTAGCAGAATAA[A/T]TTCCTTCACTCAGCA	2186
rs781844346	in-del	-/GT	1.65087e-05	0.00287299	intron-variant	BPTF	GRCh38.p7	17:67966530	ACTTAAATGGAATTA[-/GT]GTGTTTTCACTGACA	2186
rs781845147	in-del	-/C			intron-variant	BPTF	GRCh38.p7	17:67945239	GTGTAGAGACGGGGT[-/C]TCACTATGTTGCTCA	2186
rs781848051	snp	A/G/T	0.000332662	0.0128934	intron-variant, utr-variant-3-prime	BPTF	GRCh38.p7	17:67982109	AAAATTTTCTTAATC[A/G/T]TTCTTTTCTATTCGC	2186
rs781848138	snp	C/T	1.65214e-05	0.0028741	missense	BPTF	GRCh38.p7	17:67959782	ACTCCAGCTCAAAGT[C/T]CAAGAAAAAGAAAAT	2186
rs781850403	snp	A/G	1.80745e-05	0.00300615	missense	BPTF	GRCh38.p7	17:67945591	CAGCCTGAAGTTCAG[A/G]CTCAGCCTGAAGTTC	2186
rs781850688	snp	A/G	1.66635e-05	0.00288643	intron-variant	BPTF	GRCh38.p7	17:67948060	CGCCCAGCATTACAT[A/G]GGTTGTGTATTTTTC	2186
rs781852770	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67973988	GAATATTTTTTAATG[C/T]CTGACAGATAAGATT	2186
rs781852792	snp	A/G	1.64749e-05	0.00287005	intron-variant, synonymous-codon	BPTF	GRCh38.p7	17:67946079	TGTGGCTCAGATACA[A/G]GCTCAGCAAAGTGGT	2186
rs781858225	in-del	-/CAG	0.000236157	0.0108638	cds-indel	BPTF	GRCh38.p7	17:67959676	CTCCACCTTCACCTC[-/CAG]CCCCTCCACCTGCTG	2186
rs781858867	snp	C/G	2.16584e-05	0.0032907	intron-variant	BPTF	GRCh38.p7	17:67948318	GCAGGTAAGAGGGCA[C/G]ATCCTTTTCTTCTGT	2186
rs781859167	snp	A/G	1.70069e-05	0.00291602	intron-variant	BPTF	GRCh38.p7	17:67964168	ATTATAAGTAACATC[A/G]TCCCATGTGTTTTGA	2186
rs781860989	snp	A/T	1.66999e-05	0.00288958	intron-variant, missense	BPTF	GRCh38.p7	17:67946258	AAAAGAAGAAACAGC[A/T]ACAGATAGAAATTAA	2186
rs781861221	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67954564	CGGCCACCTCTTCTT[C/G]CTTCTGAATCTGGAG	2186
rs781861527	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67942801	ATAGACTTCAGCCAC[A/G]CAGAACTATGCAGAT	2186
rs781862728	snp	A/G	6.59304e-05	0.00574116	synonymous-codon	BPTF	GRCh38.p7	17:67975824	TTATGAAAAGCTGAC[A/G]GAATTTGTGGCAGAT	2186
rs781867778	snp	A/G	1.83724e-05	0.00303082	missense	BPTF	GRCh38.p7	17:67959577	AAAATTAAGAAAGAA[A/G]AAGACCTGATGCAGT	2186
rs781868093	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67979022	CTTTACAAAACACAA[A/G]AATTAGCCAGGCATG	2186
rs781868787	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67947967	TTGAACCACTCTTGA[C/T]GTTTTCCAGTCACAG	2186
rs781869146	snp	A/G			utr-variant-3-prime, downstream-variant-500B	BPTF	GRCh38.p7	17:67983497	GACCTCATCCTCTGT[A/G]TTATTTGTTGATTGG	2186
rs781869770	snp	A/G	1.64885e-05	0.00287123	missense	BPTF	GRCh38.p7	17:67964373	CAGAGAAGGATTATG[A/G]GGGGTTGAAGAGGGT	2186
rs781870914	snp	A/G	0.000378358	0.013749	intron-variant, utr-variant-3-prime	BPTF	GRCh38.p7	17:67982123	CGTTCTTTTCTATTC[A/G]CTTGCCAAGGGTGAA	2186
rs781872044	snp	A/T	3.33489e-05	0.0040833	synonymous-codon, utr-variant-3-prime	BPTF	GRCh38.p7	17:67982276	CAACAAACTGCAGTC[A/T]ACAGCTTCTTAAAGT	2186
rs781875648	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67950706	TTAGTCAGGCATGGT[A/G]GTGGGTGCCTGTAGT	2186
rs781876823	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67946499	ACTACTGTGGTGTGG[A/G]ACACTTCGTTAGATA	2186
rs781877245	snp	C/T			utr-variant-3-prime	BPTF	GRCh38.p7	17:67982761	TATAAAATCCAGCCC[C/T]GGTTACATATAATCA	2186
rs781880199	snp	C/T	1.64765e-05	0.00287019	missense	BPTF	GRCh38.p7	17:67964355	CAGTGCTCACGCCAC[C/T]AACAGAGAAGGATTA	2186
rs781881071	snp	C/T	8.04149e-05	0.00634043	missense	BPTF	GRCh38.p7	17:67959670	CCAGCCCCTCCACCT[C/T]CACCTCCCCCTCCAC	2186
rs781886350	in-del	-/A			intron-variant	BPTF	GRCh38.p7	17:67944924	CAGGGGACAGCCAAG[-/A]AGCAGGGCCCAGGCT	2186
rs781887579	snp	C/T	1.64936e-05	0.00287168	intron-variant	BPTF	GRCh38.p7	17:67966569	GCTGCTTTTTCATTA[C/T]AGGCCCATAAGATGG	2186
rs781888474	snp	A/G	1.6473e-05	0.00286988	missense	BPTF	GRCh38.p7	17:67944211	CTACTGGACAGTTGC[A/G]GTTGATACCTCAAGG	2186
rs781889476	snp	A/C	1.66679e-05	0.00288681	missense, utr-variant-3-prime	BPTF	GRCh38.p7	17:67982265	AGGTCTCATAACAAC[A/C]AACTGCAGTCTACAG	2186
rs781889582	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67958775	TTTGCAACCAGCCTG[A/G]CCAACATGGCGAAAC	2186
rs781889823	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67970093	ACAAAAGTAGCCAGG[C/T]GTGGTGGCACATGCC	2186
rs781892644	in-del	-/CCAGCCCCC/CCAGCCCCTCCAGCCCCTCCAGCCCCC	1.74974e-05	0.00295776	cds-indel	BPTF	GRCh38.p7	17:67959645	GTGACACCAGCTCCT[lengthTooLong]CCAGCCCCTCCAGCC	2186
rs781895947	in-del	-/T	0.000263708	0.0114797	intron-variant	BPTF	GRCh38.p7	17:67959504	ACATTTACATGACTC[-/T]TAATGATAGTCTTGT	2186
rs781900920	snp	A/G	1.67719e-05	0.0028958	intron-variant	BPTF	GRCh38.p7	17:67944381	GCAGCAGGTAGAGCT[A/G]TGGGTTTATCGGAAA	2186
rs781905243	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67968081	GTAATCGTATCAACA[C/T]GAATGGCTACAAATG	2186
rs781906687	snp	A/G	1.64735e-05	0.00286993	intron-variant	BPTF	GRCh38.p7	17:67940410	GCCAAGGGTGTATAA[A/G]CATTCATAATGTTTT	2186
rs781907636	snp	C/T	1.65411e-05	0.00287581	missense	BPTF	GRCh38.p7	17:67945456	CCCCAGATGCAGGTA[C/T]ATCAAGACAAAACCC	2186
rs781909793	snp	A/G	9.25677e-05	0.0068026	intron-variant	BPTF	GRCh38.p7	17:67946377	TTGAATTATTGTGCT[A/G]TGCAGTAGAATTAGT	2186
rs781911791	snp	A/G	3.29478e-05	0.00405867	missense	BPTF	GRCh38.p7	17:67945837	TCACAACCGATTCCA[A/G]TTCAACCACATACAT	2186
rs781912089	snp	C/T	1.64944e-05	0.00287175	missense	BPTF	GRCh38.p7	17:67940520	CTAACACGGTTTCCT[C/T]AACACCTGGGCAGAA	2186
rs781914191	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67958242	GAGGCTGAGGTGGGA[G/T]GATCACTTGAGCCTG	2186
rs781914376	snp	A/T	1.7782e-05	0.00298173	intron-variant	BPTF	GRCh38.p7	17:67946338	CAGGTAAAGTTATTA[A/T]GTAAAAGCAGCATGT	2186
rs781916187	snp	C/T	1.66557e-05	0.00288575	missense	BPTF	GRCh38.p7	17:67944352	GCACCACCACCACCA[C/T]TGTTTCCACGACAGC	2186
rs781919317	snp	A/G			missense	BPTF	GRCh38.p7	17:67959752	CCCAGAAGAGGAAGC[A/G]GGAAGAGGAAAAAGA	2186
rs781919328	snp	C/T	1.72797e-05	0.00293931	missense	BPTF	GRCh38.p7	17:67959857	ACTGTATCTGTAAAA[C/T]GCCTTATGATGAATC	2186
rs781920837	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67950444	GCAAATATGTTAAGC[C/G]AAGCAAAAGAAACAA	2186
rs781924437	snp	A/G	6.52273e-05	0.00571046	intron-variant, utr-variant-3-prime	BPTF	GRCh38.p7	17:67982185	CTGACCTTGGCATCC[A/G]CATAAAGCATCATTG	2186
rs781928593	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67943393	TTTTGCTTTCCAGTT[C/T]TCCAGCATGTTCCTG	2186
rs781928892	snp	A/C	1.95433e-05	0.0031259	intron-variant	BPTF	GRCh38.p7	17:67964446	CAAAATGAAATCAGC[A/C]AGCATAATTTTGGAA	2186
rs781931030	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67953188	GGATGGTCTCGATCT[C/T]CTGACCTTGTGGTCC	2186
rs781934700	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67948808	TCCTGGCCAACATGG[C/T]GAGACCTCATCCCTA	2186
rs781935365	snp	A/G	1.66827e-05	0.00288809	missense	BPTF	GRCh38.p7	17:67940471	ATGACTCAAATCATC[A/G]GGGGGCAGCCTGTCT	2186
rs781935408	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67941876	GAGTAAGAACCTCTG[G/T]TCATCAAACTCACTA	2186
rs781935993	snp	A/G			utr-variant-3-prime, downstream-variant-500B	BPTF	GRCh38.p7	17:67983412	TGCCTTCATCTGTAC[A/G]TTCTGTGATACCAGG	2186
rs781938855	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67947236	TATTTAAATGTATTA[C/T]TACCCAGCTTTACTG	2186
rs781940325	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67960741	AGAATTAGGAATGCT[G/T]AATGCCTACCTTAAG	2186
rs781943191	in-del	-/CTCAGCCTGAAGTTCAGA	0.000109977	0.0074146	cds-indel	BPTF	GRCh38.p7	17:67945573	AGCCCCAGTCCCCAG[-/CTCAGCCTGAAGTTCAGA]CTCAGCCTGAAGTTC	2186
rs781948307	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67940218	CCATTATCCTACAGA[C/T]AGCAGAGACTGGATA	2186
rs781948804	snp	A/G	1.76674e-05	0.0029721	synonymous-codon	BPTF	GRCh38.p7	17:67948285	AGCACTCCTGGACAA[A/G]GATCTGCAAATTGAA	2186
rs781949265	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67968056	AAAAAAATGGTAATA[C/G]GAGCCACGAGTAATC	2186
rs781952150	snp	C/G	1.65523e-05	0.00287678	missense	BPTF	GRCh38.p7	17:67959719	GCCTTCTGTCCACGC[C/G]CACCTTACCTGCTGC	2186
rs781952245	snp	A/G	0.0003192	0.0126293	intron-variant	BPTF	GRCh38.p7	17:67975756	CTGAAAATGTTTTAC[A/G]TTTTGTGTTTTTAAG	2186
rs781958213	snp	C/T	1.7351e-05	0.00294537	intron-variant	BPTF	GRCh38.p7	17:67976000	ATTAATTCAACTCTT[C/T]ACACTCTTTATACTA	2186
rs781958485	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67972897	CCTTACATGAACCTA[C/T]AGCATCGATGTGCCA	2186
rs781958609	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67966188	GAATGTTATCTAACA[C/T]CACGTCTCTGCTACC	2186
rs781963225	snp	A/G	1.64808e-05	0.00287057	missense	BPTF	GRCh38.p7	17:67940564	GCAACGTCCACTTCA[A/G]ATATACAGTCTTCAG	2186
rs781967040	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67954284	GTGATCCTCTTGCCT[C/T]GACCTCCCAAAGTGC	2186
rs781968045	snp	C/T	1.64732e-05	0.0028699	intron-variant, missense	BPTF	GRCh38.p7	17:67945990	CTACAAATACAGCAG[C/T]CACAGCCCCAAGTCA	2186
rs781971251	snp	A/C	1.64749e-05	0.00287005	missense	BPTF	GRCh38.p7	17:67944169	GCAATCAAGGTTTGA[A/C]AGTAGTAATTCAAGG	2186
rs781971819	snp	C/G	1.78682e-05	0.00298894	intron-variant	BPTF	GRCh38.p7	17:67945382	TGTTCCAGAGTAATA[C/G]AAATGGTTCATCTTT	2186
rs781972701	snp	A/G	0.000133508	0.00816923	intron-variant	BPTF	GRCh38.p7	17:67940398	ATTCAAAATAATGCC[A/G]AGGGTGTATAAGCAT	2186
rs781974337	snp	A/G	1.93194e-05	0.00310794	intron-variant, utr-variant-3-prime	BPTF	GRCh38.p7	17:67982212	ATTGTTTTCAAAAAT[A/G]AAGGGTGCTTAATTG	2186
rs781975552	snp	C/T			missense	BPTF	GRCh38.p7	17:67945441	CAGAGTAAACTGTCA[C/T]CCCAGATGCAGGTAC	2186
rs781978528	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67940674	AAGTAACATAAGCTT[C/T]ATTTTAACTTTAGAG	2186
rs781979416	snp	C/T			synonymous-codon	BPTF	GRCh38.p7	17:67975845	TGTGGCAGATATGAC[C/T]AAAATTTTTGATAAC	2186
rs781984945	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67965214	CAGGTGCGGTGGGGC[A/G]CACCAGTAATCCCAA	2186
rs781985510	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67980906	TGCATGCCTGTGATA[C/T]CAACACTTTGAGAAG	2186
rs781987073	snp	C/T	1.65048e-05	0.00287265	missense	BPTF	GRCh38.p7	17:67945661	CACAACCCACCCACG[C/T]ACAGTCATCCAAGCC	2186
rs781988766	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67978636	AGAAAACAAGTGGTT[C/T]AGGAAAGCAATGAGA	2186
rs781989510	snp	C/G	1.6641e-05	0.00288448	synonymous-codon	BPTF	GRCh38.p7	17:67944347	AGCCAGCACCACCAC[C/G]ACCACTGTTTCCACG	2186
rs781993899	snp	A/G	1.68863e-05	0.00290566	synonymous-codon	BPTF	GRCh38.p7	17:67945425	TACAGGTGAACAAAG[A/G]CAGAGTAAACTGTCA	2186
rs781997642	snp	C/G	1.73839e-05	0.00294816	intron-variant, missense	BPTF	GRCh38.p7	17:67946317	CAAAGTGAAATCATT[C/G]AGAAACAGGTAAAGT	2186
rs781997688	snp	C/G	1.65493e-05	0.00287652	missense	BPTF	GRCh38.p7	17:67940490	GGCAGCCTGTCTCCA[C/G]TGCAGTCTCCGCCCC	2186
rs782000934	snp	C/G	1.64741e-05	0.00286998	intron-variant, synonymous-codon	BPTF	GRCh38.p7	17:67946043	ACAAGTCCAGGTTCT[C/G]TCTCAGATCCAGTCA	2186
rs782000956	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67955574	GCTCATGCCTGTAAT[C/T]GCAGCACTTTGGGAG	2186
rs782005204	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67961336	GTTCATTCACTCCCT[A/G]TTTTAGTTGAGATGA	2186
rs782007462	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67974685	GGCTTACCGGTTTCT[C/G]AAGGACACTGCAAAG	2186
rs782008551	snp	C/T	0.000148301	0.00860978	synonymous-codon	BPTF	GRCh38.p7	17:67940590	TTCAGCCTCACAACC[C/T]CCTCGCCCCCAACAA	2186
rs782011205	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67967934	TGAATGAAATTAATG[A/G]ATGGGTTGGGGTCTC	2186
rs782011251	snp	G/T	0.000189573	0.009734	intron-variant	BPTF	GRCh38.p7	17:67947859	TCTTCTCTTTATCGT[G/T]CACACGCACAGAGTT	2186
rs782012645	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67966142	AGAATTGAAGTAACT[A/G]AAAAGAGAATCATAG	2186
rs782012864	snp	C/T	1.76173e-05	0.00296788	intron-variant	BPTF	GRCh38.p7	17:67945397	GAAATGGTTCATCTT[C/T]CCTTTTTACAGGTAC	2186
rs782012894	snp	C/T	9.4451e-05	0.00687143	intron-variant	BPTF	GRCh38.p7	17:67947840	GTCTTGTTGTCTGTC[C/T]GTCTCTTCTCTTTAT	2186
rs782013677	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67953680	TCCCAGGTTGAAGCA[A/G]TTCTCCTGCCTCAGC	2186
rs782013711	in-del	-/CTTT			intron-variant	BPTF	GRCh38.p7	17:67974153	TTGGAGATTACTGGC[-/CTTT]CTTTCACTCTCTCAG	2186
rs782016195	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67948874	ACAGCCCAGGTACTC[G/T]AGAGGCTGAGGCAGG	2186
rs782016693	snp	A/G	3.31763e-05	0.00407272	missense	BPTF	GRCh38.p7	17:67959700	CCTGCTGTGCAACAC[A/G]CAGGCCTTCTGTCCA	2186
rs782019822	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67979772	CTGGCCGGGCGCAGT[A/G]GCTCATGCCTGTAAT	2186
rs782021758	snp	C/T	6.66878e-05	0.00577403	synonymous-codon	BPTF	GRCh38.p7	17:67948252	AGAGCAGCTCAGAGC[C/T]GAGATCCTGAAGAAG	2186
rs782022652	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67952138	ACATGGTGAATCCCC[A/G]TCTCTGCTAAAGCTT	2186
rs782022893	snp	A/G	4.94181e-05	0.00497057	intron-variant, synonymous-codon	BPTF	GRCh38.p7	17:67946028	GCCTCAGCTGCAACA[A/G]CAAGTCCAGGTTCTC	2186
rs782026571	snp	A/G	1.92992e-05	0.00310632	intron-variant	BPTF	GRCh38.p7	17:67975737	TTGGAAAAACCTTAA[A/G]GCTCTGAAAATGTTT	2186
rs782027210	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67954511	CACACACAGCATGTT[A/G]GTCTCCCTTACCCCC	2186
rs782031389	snp	C/T	3.29484e-05	0.00405871	intron-variant, synonymous-codon	BPTF	GRCh38.p7	17:67946157	CAGTGCTGTGCAGAC[C/T]CACCAGATTCAGAAT	2186
rs782031892	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67973575	TGCAGTGGTGCGATC[G/T]TGGCTCACTGCAGCC	2186
rs782032820	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67975509	TTTCAAACCATTTGA[A/G]TGAAGAACGGTTCTG	2186
rs782038719	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67971024	GCTGACTGCATCCTC[A/G]TCCTCCCAGGTACAG	2186
rs782039598	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67981175	AAACAAAACAAAACA[A/C]AACAAAATTACAATG	2186
rs782040079	snp	C/T	1.71852e-05	0.00293127	missense	BPTF	GRCh38.p7	17:67959644	CAGTGACACCAGCTC[C/T]TCCAGCCCCTCCAGC	2186
rs782041475	snp	A/G	1.64746e-05	0.00287002	missense	BPTF	GRCh38.p7	17:67964339	ACAGAGGATGCCATG[A/G]CAGTGCTCACGCCAC	2186
rs782043956	in-del	-/ATA			utr-variant-3-prime	BPTF	GRCh38.p7	17:67983114	TTCAACTATGGATGT[-/ATA]ATATGAAACAAAATA	2186
rs782044707	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67948838	ACACAAAATGAAAAA[A/G]TTAGCCAGATGTGGT	2186
rs782044920	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67943397	GCTTTCCAGTTCTCC[A/G]GCATGTTCCTGGTAT	2186
rs782047103	snp	A/G	1.69109e-05	0.00290778	intron-variant, utr-variant-3-prime	BPTF	GRCh38.p7	17:67982241	TGTTCCCTTTTTTCT[A/G]TATTCTGTAGGTCTC	2186
rs782048422	snp	A/G/T			intron-variant	BPTF	GRCh38.p7	17:67969922	CAAGAGTGAAACTCC[A/G/T]TGTCAAATAAATAAA	2186
rs782048625	snp	C/T	1.64803e-05	0.00287052	missense	BPTF	GRCh38.p7	17:67940573	ACTTCAAATATACAG[C/T]CTTCAGCCTCACAAC	2186
rs782049402	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67974774	GGAGTCTCCCATGCC[C/G]TCTCTGGGCACACCA	2186
rs782054786	snp	A/G	6.58979e-05	0.00573974	intron-variant, synonymous-codon	BPTF	GRCh38.p7	17:67946151	GCAAAGCAGTGCTGT[A/G]CAGACTCACCAGATT	2186
rs782054879	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67941883	AACCTCTGTTCATCA[A/G]ACTCACTACAGAGAG	2186
rs782055877	snp	A/G	1.64735e-05	0.00286993	missense	BPTF	GRCh38.p7	17:67944181	TGACAGTAGTAATTC[A/G]AGGACAAGGTCAAAC	2186
rs782056975	snp	A/G	1.67992e-05	0.00289816	synonymous-codon	BPTF	GRCh38.p7	17:67945518	AGCAGAAGCCCAGCC[A/G]CAGACTGCTCAGCCT	2186
rs782059403	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67973393	AAAAAATAAAATATA[G/T]ATATAACAAAATTTG	2186
rs782061223	snp	A/G	1.88269e-05	0.00306808	intron-variant	BPTF	GRCh38.p7	17:67959509	TTACATGACTCTAAT[A/G]ATAGTCTTGTATTGT	2186
rs782061278	snp	C/T	1.83367e-05	0.00302787	intron-variant	BPTF	GRCh38.p7	17:67946370	CAGTAGCTTGAATTA[C/T]TGTGCTGTGCAGTAG	2186
rs782064603	snp	G/T	2.03651e-05	0.00319095	missense	BPTF	GRCh38.p7	17:67959640	CCCCCAGTGACACCA[G/T]CTCCTCCAGCCCCTC	2186
rs782064662	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67979591	GACTTTTAGAATCAC[C/T]CTATAGACAAAGCAT	2186
rs782067842	snp	G/T	3.34655e-05	0.00409043	intron-variant	BPTF	GRCh38.p7	17:67948046	CTTTCAAAATGAAAC[G/T]CCCAGCATTACATAG	2186
rs782068122	snp	C/G	1.64757e-05	0.00287012	missense	BPTF	GRCh38.p7	17:67945698	TGCAGCACAGTCTCA[C/G]CCTCAAAGTAATGTC	2186
rs782068783	snp	C/G	1.64746e-05	0.00287002	missense	BPTF	GRCh38.p7	17:67964269	GCGCTGCGTTGGCAT[C/G]TTGCAAAGTGAGGCA	2186
rs782070357	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67966262	ATCCCACCTGTTGAC[A/C]GAAGCGATTGCAATG	2186
rs782070597	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67961672	GGCAACATAGAGAGA[C/T]CCCGTCTGTACAAAA	2186
rs782076440	snp	A/G	1.64741e-05	0.00286998	synonymous-codon	BPTF	GRCh38.p7	17:67945824	TCAGACTACAACCTC[A/G]CAACCGATTCCAATT	2186
rs782077818	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67954348	CTGGTTGTCTTTTTT[C/T]CATATTACATGTTTT	2186
rs782081386	snp	A/C	1.65367e-05	0.00287543	synonymous-codon	BPTF	GRCh38.p7	17:67940494	GCCTGTCTCCACTGC[A/C]GTCTCCGCCCCTAAC	2186
rs782084527	snp	C/T	3.33167e-05	0.00408133	missense	BPTF	GRCh38.p7	17:67944349	CCAGCACCACCACCA[C/T]CACTGTTTCCACGAC	2186
rs782086380	snp	C/T	1.67581e-05	0.00289461	intron-variant	BPTF	GRCh38.p7	17:67948034	GATGTCTTAAGCCTT[C/T]CAAAATGAAACGCCC	2186
rs782086407	snp	C/T			synonymous-codon	BPTF	GRCh38.p7	17:67945773	AATACGTCCATCAAC[C/T]CCATCCCAACTGTCT	2186
rs782087667	snp	C/G	1.64912e-05	0.00287147	intron-variant, missense	BPTF	GRCh38.p7	17:67946203	GCAGCCAGTGTGCAA[C/G]AGCAGTTGCAAAGGG	2186
rs782096280	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67976040	ACGATTCAACCAGTG[C/T]AGTTTATGGTAAATT	2186
rs782096780	snp	C/T	3.4064e-05	0.00412684	intron-variant	BPTF	GRCh38.p7	17:67975768	TACATTTTGTGTTTT[C/T]AAGACCTTGCCACCA	2186
rs782097586	snp	C/G	7.27431e-05	0.00603045	missense	BPTF	GRCh38.p7	17:67945562	AGCCCCAAACCCAGC[C/G]CCAGTCCCCAGCTCA	2186
rs782098781	snp	A/G	1.6549e-05	0.0028765	synonymous-codon	BPTF	GRCh38.p7	17:67959726	GTCCACGCCCACCTT[A/G]CCTGCTGCTTCCCAG	2186
rs782100405	snp	A/G	1.89303e-05	0.00307649	missense	BPTF	GRCh38.p7	17:67948298	AAGGATCTGCAAATT[A/G]AAGTGCAGGTAAGAG	2186
rs782100840	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67981152	CTACAGAGTGAGACC[-/T]TGTTTCAAAACAAAA	2186
rs782103969	snp	C/T	1.74647e-05	0.002955	intron-variant	BPTF	GRCh38.p7	17:67976009	ACTCTTCACACTCTT[C/T]ATACTATTCTGTCTA	2186
rs782105328	snp	C/G/T	3.68835e-05	0.00429426	missense, synonymous-codon	BPTF	GRCh38.p7	17:67959559	GAGCTGAAGAGAGAC[C/G/T]TGAAAATTAAGAAAG	2186
rs782106279	snp	A/C			utr-variant-3-prime, downstream-variant-500B	BPTF	GRCh38.p7	17:67983353	TAATCCTGTTGCATC[A/C]GTTGATCATACTAAC	2186
rs782107685	snp	A/G	1.8392e-05	0.00303243	intron-variant	BPTF	GRCh38.p7	17:67959900	TCTTTTTGAGCTCTA[A/G]TTTTTTGTCTTGAAA	2186
rs782112255	snp	C/T	1.64749e-05	0.00287005	synonymous-codon	BPTF	GRCh38.p7	17:67945713	GCCTCAAAGTAATGT[C/T]CAAGGACAGTCTCCT	2186
rs782113061	snp	A/G	1.64741e-05	0.00286998	intron-variant, missense	BPTF	GRCh38.p7	17:67946159	GTGCTGTGCAGACTC[A/G]CCAGATTCAGAATGT	2186
rs782116098	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67958382	CAAAACCAAGATGGC[A/G]ATGAAAGTGACCTCT	2186
rs782119722	in-del	-/T	2.5899e-05	0.00359845	intron-variant	BPTF	GRCh38.p7	17:67948341	CTTCTGTGTCCAGTG[-/T]TTTAACATCTGAGGT	2186
rs782122112	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67961342	TCACTCCCTATTTTA[A/G]TTGAGATGAGTTAGT	2186
rs782122452	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67943846	ATTTTGTGGGGACTT[C/T]AGTTATTCAATACCT	2186
rs782123010	snp	A/G	1.6473e-05	0.00286988	synonymous-codon	BPTF	GRCh38.p7	17:67964311	TGAGTATGTCTGTCC[A/G]CAGTGCCAGTCAACA	2186
rs782124521	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67967955	TTGGGGTCTCTTTGA[C/T]CCTCTCATCCTTCTC	2186
rs782126276	snp	C/T	9.9955e-05	0.00706877	intron-variant	BPTF	GRCh38.p7	17:67947690	AACCTGTGGTGATTA[C/T]AAAATATGCGCTTTT	2186
rs782130471	snp	A/G	3.42196e-05	0.00413626	synonymous-codon	BPTF	GRCh38.p7	17:67959648	GACACCAGCTCCTCC[A/G]GCCCCTCCAGCCCCT	2186
rs782130758	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67974896	TGAGTGATTACATCA[C/T]TGGCCATTGGTGATC	2186
rs782130997	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67941955	TATCCAGAATATATA[A/G]AGAATTACTACAAAT	2186
rs782131181	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67948946	TGATGGCACCACTGC[A/C]CTGCAGCCTGGGCAA	2186
rs782132096	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67947601	ATTTTATTTATGTTA[C/T]GATATAAAATTCTTA	2186
rs782132467	snp	A/G	1.65087e-05	0.00287299	intron-variant	BPTF	GRCh38.p7	17:67966530	AACTTAAATGGAATT[A/G]GTGTTTTCACTGACA	2186
rs782132640	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67979859	CAGCCTGGCCAACAT[C/G]GTGAAACCCCGTCTA	2186
rs782133676	snp	A/T	4.504e-05	0.00474531	intron-variant	BPTF	GRCh38.p7	17:67940389	ATTATTTCAATTCAA[A/T]ATAATGCCAAGGGTG	2186
rs782133797	snp	A/G			missense	BPTF	GRCh38.p7	17:67940558	ACTTCAGCAACGTCC[A/G]CTTCAAATATACAGT	2186
rs782136149	snp	A/G	1.65375e-05	0.0028755	synonymous-codon	BPTF	GRCh38.p7	17:67959741	ACCTGCTGCTTCCCA[A/G]AAGAGGAAGCGGGAA	2186
rs782145301	snp	C/T	3.31945e-05	0.00407383	missense	BPTF	GRCh38.p7	17:67940480	ATCATCAGGGGGCAG[C/T]CTGTCTCCACTGCAG	2186
rs782145485	snp	A/T	1.64985e-05	0.0028721	missense	BPTF	GRCh38.p7	17:67975807	AGAGTACAAAGACGA[A/T]ATTATGAAAAGCTGA	2186
rs782149370	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67971140	CTGGAGTGCAGTGGC[A/G]CTATCTCGGCTCACT	2186
rs782149897	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67968082	TAATCGTATCAACAC[A/G]AATGGCTACAAATGA	2186
rs782150994	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67960037	ATTCTTACCATTGAC[A/G]CTAGTAAAGTAAAAT	2186
rs782151766	in-del	-/GC/GCC	5.01411e-05	0.00500684	frameshift-variant, cds-indel	BPTF	GRCh38.p7	17:67959684	TCACCTCCCCCTCCA[-/GC/GCC]CCTGCTGTGCAACAC	2186
rs782151775	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67954479	TTCCAACAGGGAGCC[A/G]GCTCTTATCACTGCC	2186
rs782151808	snp	C/T	1.70342e-05	0.00291836	intron-variant	BPTF	GRCh38.p7	17:67964164	CTTTATTATAAGTAA[C/T]ATCATCCCATGTGTT	2186
rs782154326	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67952696	AATGAGCCAATAGTG[A/G]TTATTATTATTATTA	2186
rs782155759	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67958257	GGATCACTTGAGCCT[A/G]GGAGGTGAAGGGTAC	2186
rs782157952	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67978603	TGCCCGGCCAGAAAT[C/T]TTTGTTTATTTGAGT	2186
rs782160717	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67950465	AAAGAAACAAAGACA[A/G]AAAATTGAGGAAAGA	2186
rs782164543	snp	C/G/T	3.46832e-05	0.00416421	missense	BPTF	GRCh38.p7	17:67945538	CTGCTCAGCCTTCAG[C/G/T]TCAGCCCCAGCCCCA	2186
rs782166783	snp	A/C	3.885e-05	0.00440721	intron-variant	BPTF	GRCh38.p7	17:67964445	TCAAAATGAAATCAG[A/C]CAGCATAATTTTGGA	2186
rs782167334	snp	C/T			intron-variant, synonymous-codon	BPTF	GRCh38.p7	17:67946094	GGCTCAGCAAAGTGG[C/T]GTGCCCCAGCAAATC	2186
rs782167494	snp	C/G	0.000181188	0.00951636	intron-variant, missense	BPTF	GRCh38.p7	17:67946029	CCTCAGCTGCAACAA[C/G]AAGTCCAGGTTCTCT	2186
rs782168201	snp	C/T	4.94181e-05	0.00497057	synonymous-codon	BPTF	GRCh38.p7	17:67944213	ACTGGACAGTTGCAG[C/T]TGATACCTCAAGGGG	2186
rs782169806	in-del	-/CCTGA			intron-variant	BPTF	GRCh38.p7	17:67953482	GCCTGATTTCAAACC[-/CCTGA]CCTGACCTCAGGTGA	2186
rs782174369	snp	C/T	3.29462e-05	0.00405857	synonymous-codon	BPTF	GRCh38.p7	17:67945764	ACAGACTCGAATACG[C/T]CCATCAACTCCATCC	2186
rs782174622	snp	C/T	1.76911e-05	0.0029741	missense	BPTF	GRCh38.p7	17:67959617	CCACAGCAGTAGCTG[C/T]ACCCTGCCCCCCAGT	2186
rs782178056	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67947602	TTTTATTTATGTTAC[A/G]ATATAAAATTCTTAC	2186
rs782178124	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67966118	TCTCCTGTCGTTATC[A/G]TAATCAGAAGAATTG	2186
rs782178994	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67953365	GTTTCAAGCGATTCT[C/T]CTGCCTCAGCCTCCC	2186
rs782179679	snp	C/T	1.67326e-05	0.00289241	synonymous-codon	BPTF	GRCh38.p7	17:67964399	AGGGTGCTCCGTTCC[C/T]TACAGGTGAGACCCC	2186
rs782182773	snp	C/G	0.000149752	0.00865179	missense	BPTF	GRCh38.p7	17:67959685	TCACCTCCCCCTCCA[C/G]CTGCTGTGCAACACA	2186
rs782185025	snp	C/T	1.65589e-05	0.00287736	synonymous-codon	BPTF	GRCh38.p7	17:67948228	GTCAGCTCTGCTCTT[C/T]AAGCACAAAGAGCAG	2186
rs782186020	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67951876	GCCTGGCTGACACGG[C/T]GAAACCCCATCTCTA	2186
rs782187506	snp	C/T	1.71997e-05	0.0029325	missense	BPTF	GRCh38.p7	17:67940444	GTTTGGGTAGGTGCT[C/T]CTCAGCAAGTGATGA	2186
rs782187699	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67952831	CACTGCCCTAACAAT[A/C]CCGTGTGCCACCTTC	2186
rs782191434	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67947336	ACAGTTCTTTAAAAT[C/T]CATTCCTGGGAAGAA	2186
rs782195191	snp	G/T			utr-variant-3-prime	BPTF	GRCh38.p7	17:67982646	TCAGTGAAGAAGCTG[G/T]TTTAGAGTCTCACAG	2186
rs782196298	snp	C/G	3.29674e-05	0.00405988	missense	BPTF	GRCh38.p7	17:67940544	GGCAGAAAAGCTTAA[C/G]TTCAGCAACGTCCAC	2186
rs782197037	in-del	-/CCCCTCCAC/CCCCTCCACCTTCACCTC/CCCCTCCAGCCCCTCCAC	0.000152534	0.00873207	cds-indel	BPTF	GRCh38.p7	17:67959658	CTCCAGCCCCTCCAG[lengthTooLong]CCCCTCCACCTTCAC	2186
rs782198273	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67953260	CCACCGCGCCTGGCC[-/T]TTTTTTTTTTTTTTG	2186
rs782199486	snp	A/T	1.73691e-05	0.00294691	missense	BPTF	GRCh38.p7	17:67959862	ATCTGTAAAACGCCT[A/T]ATGATGAATCTAAGT	2186
rs782199888	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67970892	ACATCTTTGTTTATA[C/T]ATCTGCCTGTACTTG	2186
rs782201803	snp	A/G			downstream-variant-500B	BPTF	GRCh38.p7	17:67984535	GGTATAAAGTGTTGT[A/G]TAGTTTCTATCACCA	2186
rs782201985	in-del	-/A	1.73887e-05	0.00294857	intron-variant	BPTF	GRCh38.p7	17:67966668	ATGGGTAAGTACATG[-/A]GTTGAATATGAAGTT	2186
rs782203277	snp	C/T	5.09688e-05	0.00504795	intron-variant	BPTF	GRCh38.p7	17:67975974	GTGAGCAGATGGGTT[C/T]GGTATTCTGAATTAA	2186
rs782205392	snp	C/T	3.29592e-05	0.00405938	synonymous-codon	BPTF	GRCh38.p7	17:67964251	TCAGAATTGGTACCA[C/T]GGGCGCTGCGTTGGC	2186
rs782208760	snp	C/G	1.65018e-05	0.00287239	missense	BPTF	GRCh38.p7	17:67975912	CAGTGTGCAGAAGTT[C/G]TCGAATCATTCTTTG	2186
rs782208866	snp	A/G	1.88432e-05	0.00306941	intron-variant	BPTF	GRCh38.p7	17:67959500	ATCACACATTTACAT[A/G]ACTCTAATGATAGTC	2186
rs782211855	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67980424	TTCAGATGGAGTTAA[A/G]GTAGGACAGAGGAGC	2186
rs782212832	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67964177	AACATCATCCCATGT[A/G]TTTTGAACTCACATT	2186
rs782217311	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67975295	GGTAAGACAGTATCA[C/T]TTTGTCACAAATAAA	2186
rs782218413	snp	A/G	1.83812e-05	0.00303154	intron-variant	BPTF	GRCh38.p7	17:67964433	GTGTGCAGCATTTCA[A/G]AATGAAATCAGCCAG	2186
rs782218756	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67974405	TCTCCCCATGAACAA[C/T]CAATCCAGCCTCAGA	2186
rs782218808	snp	C/T	3.92596e-05	0.00443038	intron-variant, utr-variant-3-prime	BPTF	GRCh38.p7	17:67982175	CCCAGACTGACTGAC[C/T]TTGGCATCCGCATAA	2186
rs782220352	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67965773	TGTACTGAAGACACA[A/G]AAAGCCAGTGTGGTT	2186
rs782221399	snp	A/G	1.64904e-05	0.00287139	missense	BPTF	GRCh38.p7	17:67940534	TCAACACCTGGGCAG[A/G]AAAGCTTAACTTCAG	2186
rs782222947	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67948743	CTATACTTCCAGCAG[C/T]TGGGGAGGCCAAGAC	2186
rs782227050	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67971952	AGTATTATCACTCTT[C/T]TGAGGGGTATATTTT	2186
rs782228308	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67953086	CCTGCCTCAGCTTCC[C/T]GAGTAGCTGGGACTA	2186
rs782228481	snp	A/G	4.95626e-05	0.00497784	intron-variant	BPTF	GRCh38.p7	17:67944130	TTGAACACTGTTTAC[A/G]TGTTGTGTTTTTTCC	2186
rs782230523	snp	G/T	1.77052e-05	0.00297528	utr-variant-3-prime	BPTF	GRCh38.p7	17:67982345	GGTTGTCTGAACTAT[G/T]TTAAATTAAGGAGCC	2186
rs782231062	snp	C/G	1.68792e-05	0.00290505	intron-variant, missense	BPTF	GRCh38.p7	17:67946278	ATAGAAATTAAGCGT[C/G]AACACACCCTCCAAG	2186
rs782231543	snp	A/C/G	0.000198736	0.00996649	missense	BPTF	GRCh38.p7	17:67945468	GTACATCAAGACAAA[A/C/G]CCCTGCCACCAGCTC	2186
rs782232054	snp	C/G/T	3.50013e-05	0.00418326	synonymous-codon	BPTF	GRCh38.p7	17:67945611	GCCTGAAGTTCAGAC[C/G/T]CAAACAACTGTTTCA	2186
rs782239408	snp	A/G	1.64727e-05	0.00286986	missense	BPTF	GRCh38.p7	17:67944261	CCAGGCCAGCAGCTA[A/G]TGCAAGCTGCAATGC	2186
rs782239470	snp	A/G	1.69235e-05	0.00290886	utr-variant-3-prime	BPTF	GRCh38.p7	17:67982310	GCGTGTTAACCTAAC[A/G]TAAAACACAGCAAGA	2186
rs782240320	snp	A/G	5.55859e-05	0.00527161	intron-variant	BPTF	GRCh38.p7	17:67975747	CTTAAAGCTCTGAAA[A/G]TGTTTTACATTTTGT	2186
rs782240367	snp	A/G			utr-variant-3-prime	BPTF	GRCh38.p7	17:67982522	GATGGTTTTACTATT[A/G]TGGCAGAAGCGAGAA	2186
rs782241492	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67944716	GGGTGGGTAAATCCA[G/T]TTCATGACCTCAGAT	2186
rs782243195	in-del	-/C			intron-variant	BPTF	GRCh38.p7	17:67966295	AGCATCACTCAGTGA[-/C]GGCTCATCATGTAGG	2186
rs782244857	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67951490	CACACTGTAGAAGTT[C/T]AGCATCATTTAAAGT	2186
rs782245338	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67966165	AATCATAGTCTCAAT[A/G]TGTGCTTGAATGTTA	2186
rs782247602	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67979451	ACTCAGGAGGCTGAG[A/G]CAGAATCACTTGAAC	2186
rs782247704	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67947639	TTTAAAAAAACACAT[A/G]TGTGCTCAAATTTCT	2186
rs782249679	snp	C/G	3.29457e-05	0.00405854	missense	BPTF	GRCh38.p7	17:67945756	AGTCCATCACAGACT[C/G]GAATACGTCCATCAA	2186
rs782250893	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67959378	GTTGTCTTAGTTGGG[C/T]TTAAGATATAAGAAA	2186
rs782252588	snp	A/G	1.65438e-05	0.00287605	missense	BPTF	GRCh38.p7	17:67945493	CAGCTCAGTCATCAA[A/G]TGTGGGTCCAGCAGA	2186
rs782255962	in-del	-/CCCTCCAGCCCCTCCAGA	1.68519e-05	0.0029027	cds-indel	BPTF	GRCh38.p7	17:67959659	TCCAGCCCCTCCAGC[-/CCCTCCAGCCCCTCCAGA]CCCTCCACCTTCACC	2186
rs782257112	snp	C/T	1.64836e-05	0.0028708	missense	BPTF	GRCh38.p7	17:67940550	AAAGCTTAACTTCAG[C/T]AACGTCCACTTCAAA	2186
rs782257625	snp	A/G	4.94214e-05	0.00497074	intron-variant, missense	BPTF	GRCh38.p7	17:67945967	TTTCATCCCCATCCC[A/G]TCCTCAGCTACAAAT	2186
rs782259191	snp	C/T	1.64749e-05	0.00287005	intron-variant, synonymous-codon	BPTF	GRCh38.p7	17:67946124	CAAACTCCAGTTACC[C/T]ATCCAAATTCAGCAA	2186
rs782262559	snp	C/T	1.91959e-05	0.003098	missense	BPTF	GRCh38.p7	17:67947778	AACAGAAAAAGAGCA[C/T]GACTCCAGCTGAAAG	2186
rs782266440	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67952421	GACACCTGCTACCAC[A/G]CCCAGCTTTTTTTCT	2186
rs782266891	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67963596	AAAATAAAAAGCAGA[G/T]TTTTTTCTACATTTA	2186
rs782267840	snp	C/T	5.26866e-05	0.0051323	synonymous-codon	BPTF	GRCh38.p7	17:67959675	CCCTCCACCTTCACC[C/T]CCCCCTCCACCTGCT	2186
rs782269251	snp	A/G	1.65179e-05	0.00287379	missense	BPTF	GRCh38.p7	17:67948167	AAAAACGGAAGCGTG[A/G]AGAGAGTGTGGAGCA	2186
rs782270091	snp	A/T	1.64732e-05	0.0028699	intron-variant, missense	BPTF	GRCh38.p7	17:67945954	AATCAAGTTACTGTT[A/T]CATCCCCATCCCGTC	2186
rs782270541	snp	A/T	1.73673e-05	0.00294675	intron-variant	BPTF	GRCh38.p7	17:67966666	CTATGGGTAAGTACA[A/T]GAGTTGAATATGAAG	2186
rs782273038	snp	A/G	3.30382e-05	0.00406423	missense	BPTF	GRCh38.p7	17:67948188	GTGTGGAGCAGAAAC[A/G]TAGCAAGCAGAATGC	2186
rs782273218	in-del	-/TGCTTT	1.64942e-05	0.00287173	intron-variant	BPTF	GRCh38.p7	17:67966555	TGACAATAATGATGC[-/TGCTTT]TGCTTTTTCATTATA	2186
rs782275926	snp	C/T	3.31225e-05	0.00406941	missense	BPTF	GRCh38.p7	17:67959809	AAATGATCTCTACTA[C/T]CTCAAAGGAAACTAA	2186
rs782280933	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67952986	TTTTTTTCGAGATAG[A/G]GTCTTGCTCTGTCGC	2186
rs782283532	snp	A/G	1.66543e-05	0.00288563	missense	BPTF	GRCh38.p7	17:67944342	ACCACAGCCAGCACC[A/G]CCACCACCACTGTTT	2186
rs782285348	snp	C/T	1.66065e-05	0.00288149	intron-variant	BPTF	GRCh38.p7	17:67948356	GTTTAACATCTGAGG[C/T]TCTGCTTTTTTCCCT	2186
rs782285410	snp	G/T	1.64754e-05	0.00287009	intron-variant, missense	BPTF	GRCh38.p7	17:67946093	AGGCTCAGCAAAGTG[G/T]TGTGCCCCAGCAAAT	2186
rs782285438	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67941636	GAGATGACTTTTCAG[C/T]AAATGGTGCCAGGAC	2186
rs782287595	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67948535	TAGCAACTCTGAGAG[A/G]TGAGCTTGTTGATTG	2186
rs782289586	snp	C/G			utr-variant-3-prime	BPTF	GRCh38.p7	17:67983761	TTGTCCTACCAACTT[C/G]TGGAATTTATCTAAT	2186
rs782290858	snp	C/T	1.76297e-05	0.00296893	synonymous-codon	BPTF	GRCh38.p7	17:67959624	AGTAGCTGCACCCTG[C/T]CCCCCAGTGACACCA	2186
rs782292902	snp	A/G	1.71094e-05	0.00292479	intron-variant, missense	BPTF	GRCh38.p7	17:67946293	GAACACACCCTCCAA[A/G]CTTCTAATCAAAGTG	2186
rs782293861	in-del	-/CCCAGCCCCAGT	3.60477e-05	0.0042453	cds-indel	BPTF	GRCh38.p7	17:67945555	AGCCCCAGCCCCAAA[-/CCCAGCCCCAGT]CCCAGCCCCAGTCCC	2186
rs782295342	snp	C/G	1.64735e-05	0.00286993	synonymous-codon	BPTF	GRCh38.p7	17:67945803	TCCTGGACAACAATC[C/G]CAGGTTCAGACTACA	2186
rs782296627	snp	C/T	2.0453e-05	0.00319783	intron-variant	BPTF	GRCh38.p7	17:67947856	GTCTCTTCTCTTTAT[C/T]GTGCACACGCACAGA	2186
rs782297425	snp	C/T	1.65075e-05	0.00287289	missense	BPTF	GRCh38.p7	17:67964225	AGATTTTATATTGGC[C/T]GTGATCGGTGTCAGA	2186
rs782298067	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67972381	GCTGGGATTACAGGC[A/G]CCCACCACCATACCT	2186
rs782299513	snp	C/T	0.000101735	0.00713141	intron-variant, utr-variant-3-prime	BPTF	GRCh38.p7	17:67982161	ACATGGCTGCTTCTC[C/T]CAGACTGACTGACCT	2186
rs782301732	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67967716	CCCAGCTGCTAAGGA[A/G]GCTGAGGCACAAGAA	2186
rs782304509	snp	G/T	3.29549e-05	0.00405911	utr-variant-3-prime	BPTF	GRCh38.p7	17:67982352	TGAACTATTTTAAAT[G/T]AAGGAGCCAGATGTT	2186
rs782304995	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67945089	CGCCCAGGCTGAAGC[A/G]AAGTAGCACCATTAC	2186
rs782310628	snp	C/T	1.6669e-05	0.00288691	synonymous-codon	BPTF	GRCh38.p7	17:67944338	AGCCACCACAGCCAG[C/T]ACCACCACCACCACT	2186
rs782312892	snp	C/G	1.66916e-05	0.00288886	missense	BPTF	GRCh38.p7	17:67940470	GATGACTCAAATCAT[C/G]AGGGGGCAGCCTGTC	2186
rs782313395	snp	A/C	1.70113e-05	0.00291639	intron-variant, synonymous-codon	BPTF	GRCh38.p7	17:67946286	TAAGCGTGAACACAC[A/C]CTCCAAGCTTCTAAT	2186
rs782314101	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67974484	CTACCTGAAGATAGG[A/G]TTAGATCCCACAGGT	2186
rs782318436	snp	C/T	1.76487e-05	0.00297053	missense	BPTF	GRCh38.p7	17:67959619	ACAGCAGTAGCTGCA[C/T]CCTGCCCCCCAGTGA	2186
rs782319394	in-del	-/AGG			intron-variant	BPTF	GRCh38.p7	17:67968054	AAAAAAAATGGTAAT[-/AGG]AGGAGCCACGAGTAA	2186
rs782319985	snp	A/C	1.77219e-05	0.00297668	intron-variant	BPTF	GRCh38.p7	17:67945392	TAATAGAAATGGTTC[A/C]TCTTTCCTTTTTACA	2186
rs782321356	in-del	-/AAAC			intron-variant	BPTF	GRCh38.p7	17:67980037	ACTCCGTCTGAAAAC[-/AAAC]AAACAAACAAAAAAA	2186
rs782326054	snp	A/G	1.66391e-05	0.00288431	missense	BPTF	GRCh38.p7	17:67948248	ACAAAGAGCAGCTCA[A/G]AGCCGAGATCCTGAA	2186
rs782326693	snp	A/G	9.9812e-05	0.00706371	missense	BPTF	GRCh38.p7	17:67959691	CCCCCTCCACCTGCT[A/G]TGCAACACACAGGCC	2186
rs782326759	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67980442	AGGACAGAGGAGCAC[A/G]ACTTCTCATTATAAG	2186
rs782328060	snp	C/G/T	0.000713344	0.0188723	synonymous-codon, missense	BPTF	GRCh38.p7	17:67964227	ATTTTATATTGGCTG[C/G/T]GATCGGTGTCAGAAT	2186
rs782330755	snp	C/T	3.29473e-05	0.00405864	intron-variant, missense	BPTF	GRCh38.p7	17:67946006	CACAGCCCCAAGTCA[C/T]TGCTGTGCCTCAGCT	2186
rs782332468	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67948799	TCGAGACCATCCTGG[C/T]CAACATGGCGAGACC	2186
rs782336615	in-del	-/CAAAA			intron-variant	BPTF	GRCh38.p7	17:67981157	AGTGAGACCTTGTTT[-/CAAAA]CAAAACAAAACAAAA	2186
rs782339228	in-del	-/G	6.71885e-05	0.00579567	intron-variant, utr-variant-3-prime	BPTF	GRCh38.p7	17:67982144	CAAGGGTGAATGAAA[-/G]AACATGGCTGCTTCT	2186
rs782340397	snp	C/T	1.64768e-05	0.00287021	missense	BPTF	GRCh38.p7	17:67945694	AAGTTGCAGCACAGT[C/T]TCAGCCTCAAAGTAA	2186
rs782342872	snp	A/G	3.29489e-05	0.00405874	intron-variant, missense	BPTF	GRCh38.p7	17:67946131	CAGTTACCTATCCAA[A/G]TTCAGCAAAGCAGTG	2186
rs782343619	snp	C/T	1.79738e-05	0.00299776	intron-variant	BPTF	GRCh38.p7	17:67945372	CACAGTTTTATGTTC[C/T]AGAGTAATAGAAATG	2186
rs782346759	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67953186	CAGGATGGTCTCGAT[C/T]TCCTGACCTTGTGGT	2186
rs782350491	snp	A/G	1.77647e-05	0.00298027	intron-variant	BPTF	GRCh38.p7	17:67946337	ACAGGTAAAGTTATT[A/G]AGTAAAAGCAGCATG	2186
rs782351697	snp	C/T	1.65405e-05	0.00287576	synonymous-codon	BPTF	GRCh38.p7	17:67948219	CACTAAGCTGTCAGC[C/T]CTGCTCTTCAAGCAC	2186
rs782353874	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67940007	TATAAATGCAGTTGG[A/C]CCAGAATATTCCAGA	2186
rs782354164	snp	C/T	1.884e-05	0.00306915	intron-variant	BPTF	GRCh38.p7	17:67959502	CACACATTTACATGA[C/T]TCTAATGATAGTCTT	2186
rs782357810	snp	A/G			utr-variant-3-prime	BPTF	GRCh38.p7	17:67982553	AACTTTGTTTATTGA[A/G]AAAAAAAGAAAAAGA	2186
rs782358479	snp	A/G	3.68806e-05	0.00429406	intron-variant, utr-variant-3-prime	BPTF	GRCh38.p7	17:67982179	GACTGACTGACCTTG[A/G]CATCCGCATAAAGCA	2186
rs782360487	snp	A/C/G	3.49475e-05	0.00418004	missense	BPTF	GRCh38.p7	17:67959629	CTGCACCCTGCCCCC[A/C/G]AGTGACACCAGCTCC	2186
rs782362496	snp	A/G	1.64779e-05	0.00287031	missense	BPTF	GRCh38.p7	17:67964256	ATTGGTACCATGGGC[A/G]CTGCGTTGGCATCTT	2186
rs782369843	snp	C/G	5.26977e-05	0.00513284	synonymous-codon	BPTF	GRCh38.p7	17:67959627	AGCTGCACCCTGCCC[C/G]CCAGTGACACCAGCT	2186
rs782370547	snp	C/G	0.000263548	0.0114763	missense	BPTF	GRCh38.p7	17:67945807	GGACAACAATCCCAG[C/G]TTCAGACTACAACCT	2186
rs782372305	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67959493	TGGCCAGATCACACA[C/T]TTACATGACTCTAAT	2186
rs782375967	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67957934	AATCACAATGGGTTT[G/T]TTCCTAGGGTAATAA	2186
rs782376156	snp	A/G	1.8845e-05	0.00306955	intron-variant	BPTF	GRCh38.p7	17:67959492	CTGGCCAGATCACAC[A/G]TTTACATGACTCTAA	2186
rs782376638	snp	A/G	0.000191141	0.00977414	intron-variant, utr-variant-3-prime	BPTF	GRCh38.p7	17:67982164	TGGCTGCTTCTCCCA[A/G]ACTGACTGACCTTGG	2186
rs782376667	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67964014	TTACACAGTGTTCTT[A/G]TAAATTTTTTTACTG	2186
rs782382949	snp	A/G	2.03138e-05	0.00318693	intron-variant	BPTF	GRCh38.p7	17:67947857	TCTCTTCTCTTTATC[A/G]TGCACACGCACAGAG	2186
rs782385048	in-del	-/TCCAGCCCCTCCAGCCCA	1.67722e-05	0.00289583	cds-indel	BPTF	GRCh38.p7	17:67959662	AGCCCCTCCAGCCCC[-/TCCAGCCCCTCCAGCCCA]TCCACCTTCACCTCC	2186
rs782385753	snp	G/T	1.74458e-05	0.0029534	utr-variant-3-prime	BPTF	GRCh38.p7	17:67982334	AGCAAGAATCTGGTT[G/T]TCTGAACTATTTTAA	2186
rs782388012	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67943083	ATACAGTGTTATCAT[C/G]AAAGTGAGGATAGTG	2186
rs782389267	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67980824	ATTTTCATTAAAGCA[C/T]ATGGGAGCTGAATTG	2186
rs782391484	snp	C/T	1.64836e-05	0.0028708	missense	BPTF	GRCh38.p7	17:67975823	ATTATGAAAAGCTGA[C/T]GGAATTTGTGGCAGA	2186
rs782396507	snp	C/T	1.94037e-05	0.00311472	intron-variant	BPTF	GRCh38.p7	17:67975733	CACATTGGAAAAACC[C/T]TAAAGCTCTGAAAAT	2186
rs782398353	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67941661	CAGGACAATTGAATA[C/T]ACATGGGAAACTGTG	2186
rs782398507	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67948625	AATTAGGAGCAGAGC[C/T]TCATGAGAAAGGTAC	2186
rs782398937	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67969263	ACCAGCCTGGCCAAC[A/G]TGGTGAAACCTCATC	2186
rs782401207	snp	C/T	3.76393e-05	0.004338	intron-variant	BPTF	GRCh38.p7	17:67959514	TGACTCTAATGATAG[C/T]CTTGTATTGTCTTTA	2186
rs782401777	snp	A/G	1.64732e-05	0.0028699	synonymous-codon	BPTF	GRCh38.p7	17:67944266	CCAGCAGCTAATGCA[A/G]GCTGCAATGCCAAAT	2186
rs782402128	snp	A/G	3.51377e-05	0.00419137	synonymous-codon	BPTF	GRCh38.p7	17:67959870	AACGCCTTATGATGA[A/G]TCTAAGTGAGTAGAT	2186
rs782403455	snp	A/C	1.64743e-05	0.00287	intron-variant, missense	BPTF	GRCh38.p7	17:67946155	AGCAGTGCTGTGCAG[A/C]CTCACCAGATTCAGA	2186
rs782408535	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67972394	GCGCCCACCACCATA[C/T]CTACCCAGCTAATTT	2186
rs782410441	snp	A/G	1.70009e-05	0.0029155	intron-variant	BPTF	GRCh38.p7	17:67975975	TGAGCAGATGGGTTC[A/G]GTATTCTGAATTAAT	2186
rs782411801	snp	C/T	1.64925e-05	0.00287158	intron-variant	BPTF	GRCh38.p7	17:67944144	CATGTTGTGTTTTTT[C/T]CACAGGGTGGCAATC	2186
rs782414917	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67959304	CTTTCAGTCAGCTCT[C/T]CTTTGAAGATAACTA	2186
rs782419313	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67948873	CACAGCCCAGGTACT[C/T]GAGAGGCTGAGGCAG	2186
rs782422956	snp	C/G	1.64743e-05	0.00287	intron-variant, missense	BPTF	GRCh38.p7	17:67946109	TGTGCCCCAGCAAAT[C/G]AAACTCCAGTTACCT	2186
rs782423230	snp	C/G	1.65296e-05	0.00287481	missense	BPTF	GRCh38.p7	17:67945655	CTGAAGCACAACCCA[C/G]CCACGCACAGTCATC	2186
rs782423279	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67941891	TTCATCAAACTCACT[A/G]CAGAGAGAGTGAAGA	2186
rs782427637	snp	A/G	1.65397e-05	0.00287569	missense	BPTF	GRCh38.p7	17:67948130	TTGGATAAGATAGAT[A/G]AAGAAGAAAAACAGG	2186
rs782428020	snp	C/T	1.65263e-05	0.00287452	missense	BPTF	GRCh38.p7	17:67945487	TGCCACCAGCTCAGT[C/T]ATCAAGTGTGGGTCC	2186
rs782431352	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67954280	GCAAGTGATCCTCTT[A/G]CCTCGACCTCCCAAA	2186
rs782434498	snp	A/C	4.94214e-05	0.00497074	intron-variant, missense	BPTF	GRCh38.p7	17:67946084	CTCAGATACAGGCTC[A/C]GCAAAGTGGTGTGCC	2186
rs782441352	snp	A/T	2.32183e-05	0.00340714	intron-variant	BPTF	GRCh38.p7	17:67948329	GGCACATCCTTTTCT[A/T]CTGTGTCCAGTGTTT	2186
rs782444567	snp	A/G	1.65233e-05	0.00287426	missense	BPTF	GRCh38.p7	17:67959794	AGTCCAAGAAAAAGA[A/G]AATGATCTCTACTAC	2186
rs782444594	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67960315	GAATTTGAGTGGTTC[A/G]GTTTCTTAATTGTTT	2186
rs782447683	in-del	-/C	1.64741e-05	0.00286998	frameshift-variant	BPTF	GRCh38.p7	17:67959623	AGTAGCTGCACCCTG[-/C]CCCCCCAGTGACACC	2186
rs782448339	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67972192	TTATATTTTTCTCTC[A/G]AGATATTTGGATTGT	2186
rs782448545	snp	A/G	3.36055e-05	0.00409898	synonymous-codon	BPTF	GRCh38.p7	17:67964401	GGTGCTCCGTTCCTT[A/G]CAGGTGAGACCCCTC	2186
rs782448610	in-del	-/AG			intron-variant	BPTF	GRCh38.p7	17:67949680	TATATATATACACAC[-/AG]AGACATACATATATA	2186
rs782448885	snp	A/G	1.64762e-05	0.00287016	missense	BPTF	GRCh38.p7	17:67975865	TTTTTGATAACTGTC[A/G]TTACTACAATCCAAG	2186
rs782449439	snp	C/T	3.35345e-05	0.00409465	intron-variant	BPTF	GRCh38.p7	17:67964197	GAACTCACATTTCCA[C/T]TTCGGATCTTGCAGA	2186
rs782449501	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67941516	GAGGTACAGACATAA[A/G]GAGAGGCAGATAGAC	2186
rs782449768	snp	C/T	0.000101733	0.00713133	missense	BPTF	GRCh38.p7	17:67959667	CCTCCAGCCCCTCCA[C/T]CTTCACCTCCCCCTC	2186
rs782449810	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67963235	CATTGCAGGAAGTTA[C/G]ACTGTAAAAAAGTGA	2186
rs782450213	in-del	-/CAC	0.000116456	0.00762984	cds-indel	BPTF	GRCh38.p7	17:67944337	AGCCACCACAGCCAG[-/CAC]CACCACCACCACCAC	2186
rs782451271	snp	A/G			utr-variant-3-prime, downstream-variant-500B	BPTF	GRCh38.p7	17:67983631	GTTTTTCCTTTCAGT[A/G]TTCTTACACGTTGTA	2186
rs782453565	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67958722	GGCAACAAAGCACTT[C/T]GGGAGGCCGAGGCGG	2186
rs782459473	snp	A/T	1.81562e-05	0.00301294	intron-variant	BPTF	GRCh38.p7	17:67940697	CTTTAGAGGTGATCT[A/T]ATTTATTCTTGCGGT	2186
rs782459627	snp	A/T	6.24083e-05	0.00558572	intron-variant, utr-variant-3-prime	BPTF	GRCh38.p7	17:67982149	GTGAATGAAAGAACA[A/T]GGCTGCTTCTCCCAG	2186
rs782459936	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67979304	TGTAATACCAACACT[G/T]TGGAAGGCCAAGGCA	2186
rs782461196	snp	G/T	1.82334e-05	0.00301933	missense	BPTF	GRCh38.p7	17:67959588	AGAAAAAGACCTGAT[G/T]CAGTTGGCTCAGGCC	2186
rs782462731	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67965920	AAAAAAATGAGCTGC[A/G]CATGTTGGCACGCAC	2186
rs782463023	snp	A/G	8.18431e-05	0.00639647	intron-variant, utr-variant-3-prime	BPTF	GRCh38.p7	17:67982132	CTATTCGCTTGCCAA[A/G]GGTGAATGAAAGAAC	2186
rs782469065	in-del	-/A	1.8626e-05	0.00305166	intron-variant	BPTF	GRCh38.p7	17:67959912	TAGTTTTTTGTCTTG[-/A]AAAGTTTAGCTATTA	2186
rs782471084	snp	A/C	1.65773e-05	0.00287895	missense	BPTF	GRCh38.p7	17:67945450	CTGTCACCCCAGATG[A/C]AGGTACATCAAGACA	2186
rs782471117	snp	A/G	1.67984e-05	0.00289809	utr-variant-3-prime	BPTF	GRCh38.p7	17:67982299	CTTAAAGTTCAGCGT[A/G]TTAACCTAACATAAA	2186
rs782471963	snp	A/G	0.000126016	0.00793676	intron-variant, utr-variant-3-prime	BPTF	GRCh38.p7	17:67982148	GGTGAATGAAAGAAC[A/G]TGGCTGCTTCTCCCA	2186
rs782476217	snp	C/G	0.00176846	0.0296834	missense	BPTF	GRCh38.p7	17:67959676	CCTCCACCTTCACCT[C/G]CCCCTCCACCTGCTG	2186
rs782477061	snp	A/G	3.29451e-05	0.00405851	synonymous-codon	BPTF	GRCh38.p7	17:67944230	GATACCTCAAGGGGT[A/G]ACTGTACTCCCAGGC	2186
rs782478889	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67958964	CTCAAAAAATATATA[C/T]ATGAAAAGAAAGTTA	2186
rs782479846	snp	A/G	1.67075e-05	0.00289023	synonymous-codon, utr-variant-3-prime	BPTF	GRCh38.p7	17:67982287	AGTCTACAGCTTCTT[A/G]AAGTTCAGCGTGTTA	2186
rs782480575	snp	A/G	9.88875e-05	0.00703093	intron-variant	BPTF	GRCh38.p7	17:67947700	GATTATAAAATATGC[A/G]CTTTTGGATTTATTC	2186
rs782482386	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67960256	AAGCCCTGCGAATAC[A/G]TGAAATCCTGGAAAC	2186
rs782484396	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67948003	TTTTGTCTCATCTGT[A/G]GAGGCATAGAAGAAT	2186
rs782484619	snp	C/T	1.71361e-05	0.00292707	intron-variant	BPTF	GRCh38.p7	17:67944412	TGTCGGATGTTACTA[C/T]TACACGTGGCTGGGC	2186
rs782486729	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67954202	TTGTTGTTGTCGTTG[-/T]TTTTTTTGTAGAGAC	2186
rs782489126	snp	C/T	1.64738e-05	0.00286995	intron-variant, missense	BPTF	GRCh38.p7	17:67945904	AACCCCAGGTACAGT[C/T]TTCAACTCAAACTCT	2186
rs782490760	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67946511	TGGAACACTTCGTTA[C/G]ATACATATAATATAT	2186
rs782497289	snp	A/C	1.65272e-05	0.0028746	missense	BPTF	GRCh38.p7	17:67945460	AGATGCAGGTACATC[A/C]AGACAAAACCCTGCC	2186
rs782497902	snp	C/T	1.68729e-05	0.00290451	intron-variant	BPTF	GRCh38.p7	17:67944391	GAGCTGTGGGTTTAT[C/T]GGAAATGTCGGATGT	2186
rs782502174	snp	C/T	2.10537e-05	0.00324445	intron-variant	BPTF	GRCh38.p7	17:67940411	CCAAGGGTGTATAAG[C/T]ATTCATAATGTTTTG	2186
rs782505255	snp	C/T	1.64811e-05	0.00287059	synonymous-codon	BPTF	GRCh38.p7	17:67975887	CAATCCAAGTGACTC[C/T]CCATTTTACCAGTGT	2186
rs782505561	snp	A/G	1.80097e-05	0.00300076	synonymous-codon	BPTF	GRCh38.p7	17:67945596	TGAAGTTCAGACTCA[A/G]CCTGAAGTTCAGACC	2186
rs782506249	snp	A/G	1.64735e-05	0.00286993	synonymous-codon	BPTF	GRCh38.p7	17:67945842	ACCGATTCCAATTCA[A/G]CCACATACATCTCTT	2186
rs782509215	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67952833	CTGCCCTAACAATCC[C/T]GTGTGCCACCTTCTT	2186
rs782511269	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67941357	ACTCAGGAGGCTGAG[A/G]AAGGAGAATTGCTTG	2186
rs782512561	snp	A/G	1.64909e-05	0.00287144	missense	BPTF	GRCh38.p7	17:67940528	GTTTCCTCAACACCT[A/G]GGCAGAAAAGCTTAA	2186
rs782516232	snp	A/C	4.95659e-05	0.004978	synonymous-codon	BPTF	GRCh38.p7	17:67959777	AAAAGACTCCAGCTC[A/C]AAGTCCAAGAAAAAG	2186
rs782517743	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67976442	CACACCACTGCATTC[C/T]AGCCTGGGTGACAAT	2186
rs782518078	snp	A/G	4.94352e-05	0.00497143	missense	BPTF	GRCh38.p7	17:67975834	CTGACGGAATTTGTG[A/G]CAGATATGACCAAAA	2186
rs782520146	snp	A/G	1.66374e-05	0.00288417	intron-variant	BPTF	GRCh38.p7	17:67948069	TTACATAGGTTGTGT[A/G]TTTTTCTCTAGAATG	2186
rs782520314	snp	C/T	4.94189e-05	0.00497062	missense	BPTF	GRCh38.p7	17:67945762	TCACAGACTCGAATA[C/T]GTCCATCAACTCCAT	2186
rs782521728	snp	A/G	1.68946e-05	0.00290638	missense	BPTF	GRCh38.p7	17:67940453	GGTGCTCCTCAGCAA[A/G]TGATGACTCAAATCA	2186
rs782523259	snp	C/G/T	0.000197669	0.0099397	intron-variant, missense	BPTF	GRCh38.p7	17:67946080	GTGGCTCAGATACAG[C/G/T]CTCAGCAAAGTGGTG	2186
rs782524127	in-del	-/T	1.83209e-05	0.00302657	intron-variant	BPTF	GRCh38.p7	17:67940429	CATAATGTTTTGCTG[-/T]TTTGGGTAGGTGCTC	2186
rs782525305	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67960533	GTGATATAAACAAGA[C/T]TATAGAGGCACTAAA	2186
rs782525880	snp	G/T	1.64751e-05	0.00287007	intron-variant, missense	BPTF	GRCh38.p7	17:67946062	CAGATCCAGTCACAG[G/T]TTGTGGCTCAGATAC	2186
rs782527373	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67971895	AGCTTCCACTAATAG[C/T]GTATATCTATGGCAT	2186
rs782528228	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67951462	ACTTTGGCCTCTTGA[A/G]CAAGCCAGTTTACAC	2186
rs782530675	snp	A/G	3.29451e-05	0.00405851	synonymous-codon	BPTF	GRCh38.p7	17:67944248	TGTACTCCCAGGCCC[A/G]GGCCAGCAGCTAATG	2186
rs782531967	snp	C/T	5.05174e-05	0.00502555	intron-variant, missense	BPTF	GRCh38.p7	17:67946275	CAGATAGAAATTAAG[C/T]GTGAACACACCCTCC	2186
rs782536000	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67970174	GGAGGTGGAGGTTGC[A/G]GTGAGCTGAGATCAC	2186
rs782537611	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67980028	CAAGAGTGAGACTCC[A/G]TCTGAAAACAAACAA	2186
rs782537973	snp	C/G/T	6.71483e-05	0.00579399	missense	BPTF	GRCh38.p7	17:67959673	GCCCCTCCACCTTCA[C/G/T]CTCCCCCTCCACCTG	2186
rs782539445	snp	A/G	1.83889e-05	0.00303218	missense	BPTF	GRCh38.p7	17:67959574	CTGAAAATTAAGAAA[A/G]AAAAAGACCTGATGC	2186
rs782541075	snp	C/T	1.64735e-05	0.00286993	missense	BPTF	GRCh38.p7	17:67945744	GTTCGTGTCCAAAGT[C/T]CATCACAGACTCGAA	2186
rs782541649	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67970664	TTTGAGGATATAAGG[A/G]AACCAACAAAATCAG	2186
rs782543818	snp	C/T	1.64732e-05	0.0028699	intron-variant, missense	BPTF	GRCh38.p7	17:67945955	ATCAAGTTACTGTTT[C/T]ATCCCCATCCCGTCC	2186
rs782545968	snp	C/T			utr-variant-3-prime	BPTF	GRCh38.p7	17:67982428	ATTGGTCATAACAGT[C/T]CAATTATATTCTTGG	2186
rs782546126	snp	A/G	1.66801e-05	0.00288787	synonymous-codon	BPTF	GRCh38.p7	17:67959825	CTCAAAGGAAACTAA[A/G]AAGGACACAAAGCTT	2186
rs782549795	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67968521	CGGTGGCTCACGCCT[A/G]TAATACCAGCACTTT	2186
rs782550362	snp	A/G	3.44193e-05	0.00414831	intron-variant	BPTF	GRCh38.p7	17:67944418	ATGTTACTACTACAC[A/G]TGGCTGGGCTAACAG	2186
rs782550647	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67944588	TCCCTCCTATTAAAA[A/G]AGAGAGAGAGAGAAA	2186
rs782551259	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67947877	CACGCACAGAGTTCT[A/G]AGTTTATACTTGTTT	2186
rs782553611	snp	A/G	1.64773e-05	0.00287026	missense	BPTF	GRCh38.p7	17:67964357	GTGCTCACGCCACTA[A/G]CAGAGAAGGATTATG	2186
rs782554659	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67974210	TTTTATTTCAAACAC[A/G]TCGTTCTCCTAGGAT	2186
rs782555929	snp	A/T	1.74124e-05	0.00295057	synonymous-codon	BPTF	GRCh38.p7	17:67940440	TGCTGTTTGGGTAGG[A/T]GCTCCTCAGCAAGTG	2186
rs782556573	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67940770	GCTGATTTGAAGAAA[G/T]GGTTGCTTCCTGGAG	2186
rs782560793	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67979320	TGGAAGGCCAAGGCA[C/T]GTGGATCATCTGAGA	2186
rs782564344	snp	A/G	1.65899e-05	0.00288005	synonymous-codon	BPTF	GRCh38.p7	17:67966607	TTTCCTTGAACCAGT[A/G]GACCCTAATGATGCA	2186
rs782564670	snp	A/G	1.76076e-05	0.00296707	intron-variant	BPTF	GRCh38.p7	17:67966680	ATGAGTTGAATATGA[A/G]GTTTTTCAGAAGTCT	2186
rs782567198	snp	A/G	1.675e-05	0.00289391	missense	BPTF	GRCh38.p7	17:67975955	AAGGCTTCAAAGCTA[A/G]CAGGTGAGCAGATGG	2186
rs782567803	snp	A/C	9.88435e-05	0.00702937	missense	BPTF	GRCh38.p7	17:67945726	GTCCAAGGACAGTCT[A/C]CTGTTCGTGTCCAAA	2186
rs782570930	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67972288	TCACCCAGGCTGGAG[C/T]GCAGTGTCGTGATCT	2186
rs782572192	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67974518	GTACTCAGTCCCCAA[A/G]ATTACCCCCTCTTCA	2186
rs782574787	snp	C/T	4.94189e-05	0.00497062	intron-variant, missense	BPTF	GRCh38.p7	17:67945919	CTTCAACTCAAACTC[C/T]TTCATCAGGACAAAC	2186
rs782578733	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67968368	TAGAAGGAGTTAATC[A/G]TTGTACATATTTCAA	2186
rs782581414	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67965992	CTTGAGCACAGGAGG[C/T]TACAGTGAGCTATGA	2186
rs782581864	snp	C/G	3.30447e-05	0.00406464	missense	BPTF	GRCh38.p7	17:67945483	ACCCTGCCACCAGCT[C/G]AGTCATCAAGTGTGG	2186
rs782582078	in-del	-/AGCCCCTCCAGCCCCTCA	1.68539e-05	0.00290287	cds-indel	BPTF	GRCh38.p7	17:67959656	TCCTCCAGCCCCTCC[-/AGCCCCTCCAGCCCCTCA]AGCCCCTCCACCTTC	2186
rs782583967	snp	A/G	1.71652e-05	0.00292955	intron-variant	BPTF	GRCh38.p7	17:67944416	GGATGTTACTACTAC[A/G]CGTGGCTGGGCTAAC	2186
rs782589989	snp	A/G	1.6528e-05	0.00287467	missense	BPTF	GRCh38.p7	17:67948139	ATAGATAAAGAAGAA[A/G]AACAGGCAGCAAAAA	2186
rs782590414	snp	C/T	1.64754e-05	0.00287009	intron-variant, synonymous-codon	BPTF	GRCh38.p7	17:67946091	ACAGGCTCAGCAAAG[C/T]GGTGTGCCCCAGCAA	2186
rs782590739	snp	A/G	0.000654042	0.0180719	intron-variant, utr-variant-3-prime	BPTF	GRCh38.p7	17:67982187	GACCTTGGCATCCGC[A/G]TAAAGCATCATTGTT	2186
rs782591011	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67959021	TATGTTGCACTACTC[G/T]CCCTGCAGTCTGAAA	2186
rs782591073	snp	A/G	1.7144e-05	0.00292775	missense	BPTF	GRCh38.p7	17:67945621	CAGACCCAAACAACT[A/G]TTTCATCCCATGTCC	2186
rs782592058	snp	A/G	1.65729e-05	0.00287857	intron-variant	BPTF	GRCh38.p7	17:67944112	TACATACAGATTGAT[A/G]CTTTGAACACTGTTT	2186
rs782594079	snp	A/G	3.36836e-05	0.00410374	intron-variant, missense	BPTF	GRCh38.p7	17:67946276	AGATAGAAATTAAGC[A/G]TGAACACACCCTCCA	2186
rs782594901	snp	A/T	1.65315e-05	0.00287498	missense	BPTF	GRCh38.p7	17:67959799	AAGAAAAAGAAAATG[A/T]TCTCTACTACCTCAA	2186
rs782598045	in-del	-/T	1.90991e-05	0.00309018	intron-variant	BPTF	GRCh38.p7	17:67959925	TTGAAAGTTTAGCTA[-/T]TAAATTGGATTTTGA	2186
rs782604446	snp	C/G	5.09273e-05	0.00504589	intron-variant	BPTF	GRCh38.p7	17:67964175	GTAACATCATCCCAT[C/G]TGTTTTGAACTCACA	2186
rs782607117	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67962686	TGCCATATTCCATTA[G/T]GAGAGGTTATTTTTA	2186
rs782610085	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67941395	GAGGCGGAGGTTGTA[G/T]TGAGCTGAGATTGCA	2186
rs782611352	snp	A/G	3.29457e-05	0.00405854	missense	BPTF	GRCh38.p7	17:67945763	CACAGACTCGAATAC[A/G]TCCATCAACTCCATC	2186
rs782614278	snp	C/G	1.67103e-05	0.00289048	synonymous-codon	BPTF	GRCh38.p7	17:67964398	GAGGGTGCTCCGTTC[C/G]TTACAGGTGAGACCC	2186
rs782617557	snp	C/G	1.6492e-05	0.00287154	intron-variant	BPTF	GRCh38.p7	17:67948327	AGGGCACATCCTTTT[C/G]TTCTGTGTCCAGTGT	2186
rs782618552	snp	A/T	1.65274e-05	0.00287462	synonymous-codon	BPTF	GRCh38.p7	17:67945488	GCCACCAGCTCAGTC[A/T]TCAAGTGTGGGTCCA	2186
rs782620109	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67960575	GTTTCATTTTTTTGG[G/T]CATTACTATCATTTT	2186
rs782620888	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67964030	TAAATTTTTTTACTG[C/T]TTGTTCTTAACATCA	2186
rs782623517	snp	A/C	1.66757e-05	0.00288749	intron-variant, utr-variant-3-prime	BPTF	GRCh38.p7	17:67982145	AAGGGTGAATGAAAG[A/C]ACATGGCTGCTTCTC	2186
rs782623728	in-del	-/AC			intron-variant	BPTF	GRCh38.p7	17:67969441	GGGCAACAGAGAAAA[-/AC]ACTCTGTCTCCAAAA	2186
rs782623738	snp	A/G	1.79329e-05	0.00299435	missense	BPTF	GRCh38.p7	17:67959604	CAGTTGGCTCAGGCC[A/G]CAGCAGTAGCTGCAC	2186
rs782626516	snp	C/T	1.67489e-05	0.00289381	synonymous-codon	BPTF	GRCh38.p7	17:67959681	ACCTTCACCTCCCCC[C/T]CCACCTGCTGTGCAA	2186
rs782627972	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67958839	GGGTGTGGTGTTGCA[C/T]GCCTGTAATCCCAGC	2186
rs782633181	snp	G/T	1.67405e-05	0.00289309	utr-variant-3-prime	BPTF	GRCh38.p7	17:67982290	CTACAGCTTCTTAAA[G/T]TTCAGCGTGTTAACC	2186
rs782633438	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67965735	GGATAGGGATGGTTT[G/T]CAGGATTATCAAGTG	2186
rs782633592	snp	A/G	1.64808e-05	0.00287057	synonymous-codon	BPTF	GRCh38.p7	17:67964365	GCCACTAACAGAGAA[A/G]GATTATGAGGGGTTG	2186
rs782633769	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67955163	AGGCATGGTGGTGGG[C/T]GCTACTTGGGAGGCT	2186
rs782638148	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67977477	CTGAGATTGCGCCAC[C/T]GCATTCCAGCCTTGG	2186
rs782639578	snp	C/T	3.29478e-05	0.00405867	intron-variant, missense	BPTF	GRCh38.p7	17:67945966	GTTTCATCCCCATCC[C/T]GTCCTCAGCTACAAA	2186
rs782640519	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67962402	TATAGACACACTGTG[-/T]TAAGCGTTTGTTACA	2186
rs782641892	snp	A/G	3.29826e-05	0.00406082	synonymous-codon	BPTF	GRCh38.p7	17:67975905	ATTTTACCAGTGTGC[A/G]GAAGTTCTCGAATCA	2186
rs782648357	snp	A/C	7.99552e-05	0.00632228	intron-variant, utr-variant-3-prime	BPTF	GRCh38.p7	17:67982174	TCCCAGACTGACTGA[A/C]CTTGGCATCCGCATA	2186
rs782649280	snp	A/G	1.64749e-05	0.00287005	intron-variant, missense	BPTF	GRCh38.p7	17:67946117	AGCAAATCAAACTCC[A/G]GTTACCTATCCAAAT	2186
rs782651095	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67953066	CCCCGGGTTCACGCC[A/G]GTCTCCTGCCTCAGC	2186
rs782651665	snp	C/T	1.65222e-05	0.00287417	synonymous-codon	BPTF	GRCh38.p7	17:67945464	GCAGGTACATCAAGA[C/T]AAAACCCTGCCACCA	2186
rs782655578	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67942757	TTAGCTAAGTAAATT[G/T]TAGTATATTCCTACA	2186
rs782655762	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67949417	CTGTCTCTACTAAAA[A/G]TACAAAAATTAGCTG	2186
rs782655819	snp	A/G	1.64906e-05	0.00287142	synonymous-codon	BPTF	GRCh38.p7	17:67940530	TTCCTCAACACCTGG[A/G]CAGAAAAGCTTAACT	2186
rs782657155	snp	A/C	1.64974e-05	0.00287201	synonymous-codon	BPTF	GRCh38.p7	17:67964231	TATATTGGCTGTGAT[A/C]GGTGTCAGAATTGGT	2186
rs782657459	snp	A/G			utr-variant-3-prime	BPTF	GRCh38.p7	17:67982472	ACGGACAAGAAAAAA[A/G]CAAAGTCAACGACAC	2186
rs782657570	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67951468	GCCTCTTGAACAAGC[C/G]AGTTTACACACTGTA	2186
rs782657986	snp	A/T	1.65378e-05	0.00287552	missense	BPTF	GRCh38.p7	17:67964217	GATCTTGCAGATTTT[A/T]TATTGGCTGTGATCG	2186
rs782660488	snp	C/T	1.76179e-05	0.00296793	missense	BPTF	GRCh38.p7	17:67959620	CAGCAGTAGCTGCAC[C/T]CTGCCCCCCAGTGAC	2186
rs782662541	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67975129	AAATGGGGACAAAAA[A/C]CAAATATATATTTCA	2186
rs782663433	snp	A/C/G	3.29567e-05	0.00405924	missense	BPTF	GRCh38.p7	17:67975879	CGTTACTACAATCCA[A/C/G]GTGACTCCCCATTTT	2186
rs782665261	snp	A/G			utr-variant-3-prime	BPTF	GRCh38.p7	17:67984005	AAGACTAATCGCTCA[A/G]TATGAAAACATGAAA	2186
rs782665716	snp	A/G	1.70872e-05	0.00292289	intron-variant, synonymous-codon	BPTF	GRCh38.p7	17:67946292	TGAACACACCCTCCA[A/G]GCTTCTAATCAAAGT	2186
rs782668198	snp	A/C	5.19926e-05	0.00509839	intron-variant, utr-variant-3-prime	BPTF	GRCh38.p7	17:67982160	AACATGGCTGCTTCT[A/C]CCAGACTGACTGACC	2186
rs782668767	snp	A/T	1.68371e-05	0.00290143	utr-variant-3-prime	BPTF	GRCh38.p7	17:67982303	AAGTTCAGCGTGTTA[A/T]CCTAACATAAAACAC	2186
rs782672538	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67970827	CAGCCCCCATCAATA[G/T]ATTTTTTTATTGTGT	2186
rs782675372	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67980066	AAAACCTACCCAGGC[C/T]GGGTGTGGTGGCTTA	2186
rs782676721	snp	A/C/G	4.97635e-05	0.00498795	intron-variant	BPTF	GRCh38.p7	17:67944100	ATAAAAATGATATAC[A/C/G]TACAGATTGATGCTT	2186
rs782677403	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67960324	TGGTTCGGTTTCTTA[A/G]TTGTTTTATTTTAAG	2186
rs782680526	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67963564	CAAATTGCTCTGACT[A/G]GTTACTTATTTATTT	2186
rs782680743	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67968574	ACGAGGTCAGGAGAT[C/T]GAGACCATCCTGGCT	2186
rs782681187	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67967203	CTGGAGTGTACTAGC[A/G]CGATCTCACATCACT	2186
rs782685120	in-del	-/A	1.70095e-05	0.00291625	intron-variant	BPTF	GRCh38.p7	17:67940662	CAGGGCCACGTAAGT[-/A]AACATAAGCTTTATT	2186
rs782685681	snp	A/G	1.6473e-05	0.00286988	missense	BPTF	GRCh38.p7	17:67945753	CAAAGTCCATCACAG[A/G]CTCGAATACGTCCAT	2186
rs782686284	snp	A/G	3.67539e-05	0.00428668	synonymous-codon	BPTF	GRCh38.p7	17:67959576	GAAAATTAAGAAAGA[A/G]AAAGACCTGATGCAG	2186
rs782690985	snp	C/T	1.68681e-05	0.00290409	missense	BPTF	GRCh38.p7	17:67940454	GTGCTCCTCAGCAAG[C/T]GATGACTCAAATCAT	2186
rs782691018	snp	A/G	1.65979e-05	0.00288074	intron-variant, missense	BPTF	GRCh38.p7	17:67946243	TCAGGGATCAGCAGC[A/G]AAAGAAGAAACAGCA	2186
rs782691095	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67948426	AGAACTTACATTTGT[A/G]TACATAGAGTAAAAA	2186
rs782692669	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67942969	TGCCTGCCTGGAGGG[A/G]GCACTATTCCCATTG	2186
rs782693376	snp	G/T	3.94081e-05	0.00443875	synonymous-codon	BPTF	GRCh38.p7	17:67948303	TCTGCAAATTGAAGT[G/T]CAGGTAAGAGGGCAC	2186
rs782695058	snp	A/G	3.30169e-05	0.00406293	intron-variant, missense	BPTF	GRCh38.p7	17:67946216	AAGAGCAGTTGCAAA[A/G]GGTTCAGCAACTCAG	2186
rs782698424	snp	C/T			missense	BPTF	GRCh38.p7	17:67959668	CTCCAGCCCCTCCAC[C/T]TTCACCTCCCCCTCC	2186
rs782701696	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67979986	GCGGAGGTTGCAGAT[C/T]GCACCACTACACTCT	2186
rs782702548	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67954386	AAACATTTAAGTTTT[A/G]CAAGCTTATTTTGAG	2186
rs782703184	snp	C/T	1.67005e-05	0.00288963	synonymous-codon	BPTF	GRCh38.p7	17:67975779	TTTTTAAGACCTTGC[C/T]ACCATGGAAGAAAGA	2186
rs782703860	snp	C/G	1.67041e-05	0.00288994	missense, utr-variant-3-prime	BPTF	GRCh38.p7	17:67982256	ATATTCTGTAGGTCT[C/G]ATAACAACAAACTGC	2186
rs782707556	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67978113	CCCACCTCGGCCTCC[C/T]AAAGTGCTGGGATTA	2186
rs782708217	snp	C/G	1.88998e-05	0.00307401	intron-variant	BPTF	GRCh38.p7	17:67959922	GTCTTGAAAGTTTAG[C/G]TATTAAATTGGATTT	2186
rs782710342	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67947841	TCTTGTTGTCTGTCC[A/G]TCTCTTCTCTTTATC	2186
rs782710943	snp	C/T	1.84899e-05	0.0030405	intron-variant	BPTF	GRCh38.p7	17:67947714	CGCTTTTGGATTTAT[C/T]CTGTCCTGAAGGTGG	2186
rs782711414	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67952647	CACACACAATTTCCC[C/T]TATTAATGTTAGCAT	2186
rs782712478	snp	A/T	0.000251857	0.011219	intron-variant, utr-variant-3-prime	BPTF	GRCh38.p7	17:67982085	TGAAAAGTTTTAATA[A/T]TATAGGTTAAAATTT	2186
rs782714549	snp	G/T			intron-variant, missense	BPTF	GRCh38.p7	17:67945941	AGGACAAACTTTAAA[G/T]CAAGTTACTGTTTCA	2186
rs782716099	snp	A/G	3.29462e-05	0.00405857	missense	BPTF	GRCh38.p7	17:67944189	GTAATTCAAGGACAA[A/G]GTCAAACTACTGGAC	2186
rs782716690	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67966758	AGCAAGGCTGGTGGG[G/T]GTATAAATTGGTATG	2186
rs782716773	in-del	ACTGCATTCCAGCCTGGGAGACAGAGCGAGACTCCATCTC/CGGGGGAAAAGGGGAAGACCCCCCCAAAAA			intron-variant	BPTF	GRCh38.p7	17:67956279	AGCCGAGATTGCGCC[lengthTooLong]AAAAAAAAAAAAAAA	2186
rs782717141	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67940736	AAACATGAACTTATT[G/T]TGATACGTTTTTAAA	2186
rs782720448	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67942609	ATGCCCAAGGTCCCA[A/G]TATACCTTCTAGGTA	2186
rs782720627	in-del	-/A			intron-variant	BPTF	GRCh38.p7	17:67971484	TGAGACGCTGTCTTT[-/A]AAAAAAAAAAAAAAG	2186
rs782723297	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67978724	ATCCTAGCAGGAGAA[A/T]GGAGCACTCCCCAGA	2186
rs782724886	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67976163	GTTGTTGATCTACTT[A/G]AAGTCTTTTTTTGAA	2186
rs782727606	snp	C/T	1.69703e-05	0.00291288	synonymous-codon	BPTF	GRCh38.p7	17:67959651	ACCAGCTCCTCCAGC[C/T]CCTCCAGCCCCTCCA	2186
rs782727607	snp	A/G	1.65081e-05	0.00287293	intron-variant	BPTF	GRCh38.p7	17:67966533	TTAAATGGAATTAGT[A/G]TTTTCACTGACAATA	2186
rs782728329	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67974148	GATTGATTGGAGATT[A/C]CTGGCCTTTCACTCT	2186
rs782729018	snp	C/G/T	5.22565e-05	0.00511136	intron-variant, utr-variant-3-prime	BPTF	GRCh38.p7	17:67982227	GAAGGGTGCTTAATT[C/G/T]TTCCCTTTTTTCTAT	2186
rs782729053	snp	A/G	3.31813e-05	0.00407302	missense	BPTF	GRCh38.p7	17:67948088	TTCTCTAGAATGATT[A/G]TCTGTAACCAGGTGA	2186
rs782730444	snp	C/T	1.6495e-05	0.0028718	intron-variant	BPTF	GRCh38.p7	17:67966558	ACAATAATGATGCTG[C/T]TTTTTCATTATAGGC	2186
rs782730693	in-del	-/A			intron-variant	BPTF	GRCh38.p7	17:67944735	TGACCTCAGATTGAG[-/A]AGTGGGTCCAGAACC	2186
rs782731546	snp	C/T	1.64741e-05	0.00286998	missense	BPTF	GRCh38.p7	17:67945829	CTACAACCTCACAAC[C/T]GATTCCAATTCAACC	2186
rs782733757	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67965384	ATGGTTTGCAGGATT[A/G]GCAAGTGATAGAGAT	2186
rs782735412	snp	A/G			utr-variant-3-prime, downstream-variant-500B	BPTF	GRCh38.p7	17:67983513	TTATTTGTTGATTGG[A/G]TTTGTTTTCTGTTTG	2186
rs782735641	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67952834	TGCCCTAACAATCCC[A/G]TGTGCCACCTTCTTG	2186
rs782736819	snp	A/C	1.65211e-05	0.00287407	missense	BPTF	GRCh38.p7	17:67959778	AAAGACTCCAGCTCA[A/C]AGTCCAAGAAAAAGA	2186
rs782736894	snp	C/T	1.64773e-05	0.00287026	missense	BPTF	GRCh38.p7	17:67975841	AATTTGTGGCAGATA[C/T]GACCAAAATTTTTGA	2186
rs782741201	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67946587	TGGGAAGAATGGAGT[G/T]ATGAGCTTTAATCTT	2186
rs782746177	snp	A/G	6.70219e-05	0.00578848	intron-variant	BPTF	GRCh38.p7	17:67948036	TGTCTTAAGCCTTTC[A/G]AAATGAAACGCCCAG	2186
rs782750355	snp	C/T	1.67604e-05	0.00289481	synonymous-codon	BPTF	GRCh38.p7	17:67940656	GTTAACACAGGGCCA[C/T]GTAAGTAACATAAGC	2186
rs782750363	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67950968	ATGTGCCACCATGCC[C/T]GGCTAATTTTTTGTA	2186
rs782752000	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67942018	GAAAAAAGACAAACA[C/G]GCAAGGTGCGGTGGC	2186
rs782755462	snp	C/T	9.95272e-05	0.00705363	intron-variant, utr-variant-3-prime	BPTF	GRCh38.p7	17:67982120	AATCGTTCTTTTCTA[C/T]TCGCTTGCCAAGGGT	2186
rs782755996	snp	C/T	3.29468e-05	0.00405861	intron-variant, missense	BPTF	GRCh38.p7	17:67946041	CAACAAGTCCAGGTT[C/T]TCTCTCAGATCCAGT	2186
rs782759187	snp	A/G	1.66576e-05	0.00288592	missense	BPTF	GRCh38.p7	17:67944351	AGCACCACCACCACC[A/G]CTGTTTCCACGACAG	2186
rs782759745	snp	A/C			intron-variant	BPTF	GRCh38.p7	17:67949045	TCTGTAGGTATTGCT[A/C]ACCTGCTTTCTAGAG	2186
rs782760190	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67940670	ACGTAAGTAACATAA[A/G]CTTTATTTTAACTTT	2186
rs782760282	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67970189	GGTGAGCTGAGATCA[C/T]GCCATTGCACTCCTC	2186
rs782760428	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67979893	TAAAATAAAAAAATT[A/T]GCTAGGTGTGGTGGT	2186
rs782760453	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67967390	TGTGATCCGCTCCCC[C/T]TCGGCCTCCCCAAAG	2186
rs782763517	snp	A/G	1.65512e-05	0.00287669	missense	BPTF	GRCh38.p7	17:67940489	GGGCAGCCTGTCTCC[A/G]CTGCAGTCTCCGCCC	2186
rs782768375	snp	A/G	1.64749e-05	0.00287005	intron-variant, missense	BPTF	GRCh38.p7	17:67946168	AGACTCACCAGATTC[A/G]GAATGTGGTTACAGT	2186
rs782770116	snp	A/G	1.64727e-05	0.00286986	synonymous-codon	BPTF	GRCh38.p7	17:67944224	GCAGTTGATACCTCA[A/G]GGGGTGACTGTACTC	2186
rs782770324	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67960058	AAAGTAAAATTTGCT[A/G]TTTCACGTGTTTGTG	2186
rs782773177	snp	A/C			missense	BPTF	GRCh38.p7	17:67947742	TGGTGATGAAGCATA[A/C]TGCTGTAATAGAACA	2186
rs782774616	snp	A/G	1.64741e-05	0.00286998	synonymous-codon	BPTF	GRCh38.p7	17:67964329	GTGCCAGTCAACAGA[A/G]GATGCCATGACAGTG	2186
rs782776233	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67971314	GAACTCCTGACCTCA[A/G]GGGATCCACCTGCCT	2186
rs782779638	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67976502	CCCAGCCTTGTCAAC[A/G]TAATGAGACCATGTC	2186
rs782782569	snp	G/T	3.34197e-05	0.00408763	missense	BPTF	GRCh38.p7	17:67944369	GTTTCCACGACAGCA[G/T]CAGGTAGAGCTGTGG	2186
rs782785097	snp	G/T			intron-variant	BPTF	GRCh38.p7	17:67966470	TTTCATGTATCAAAT[G/T]TAAAACTCACTTTTG	2186
rs782787976	snp	C/T	5.08023e-05	0.0050397	intron-variant	BPTF	GRCh38.p7	17:67944400	GTTTATCGGAAATGT[C/T]GGATGTTACTACTAC	2186
rs782788697	snp	A/C	4.96298e-05	0.00498121	synonymous-codon	BPTF	GRCh38.p7	17:67945455	ACCCCAGATGCAGGT[A/C]CATCAAGACAAAACC	2186
rs782789451	snp	A/G	8.23716e-05	0.00641709	missense	BPTF	GRCh38.p7	17:67945717	CAAAGTAATGTCCAA[A/G]GACAGTCTCCTGTTC	2186
rs782791308	snp	C/T	1.64754e-05	0.00287009	missense	BPTF	GRCh38.p7	17:67945699	GCAGCACAGTCTCAG[C/T]CTCAAAGTAATGTCC	2186
rs782792628	snp	C/T			intron-variant, synonymous-codon	BPTF	GRCh38.p7	17:67946160	TGCTGTGCAGACTCA[C/T]CAGATTCAGAATGTG	2186
rs782793228	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67978830	GCCAAAGAACGTCAG[A/G]GATAAAAATGAAAGG	2186
rs782794319	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67947893	AGTTTATACTTGTTT[A/G]TCTTGATTGAAGTTC	2186
rs782794869	snp	A/G	2.01258e-05	0.00317214	intron-variant	BPTF	GRCh38.p7	17:67964450	ATGAAATCAGCCAGC[A/G]TAATTTTGGAAGCAT	2186
rs782797376	snp	C/G	6.92533e-05	0.00588403	missense	BPTF	GRCh38.p7	17:67959641	CCCCAGTGACACCAG[C/G]TCCTCCAGCCCCTCC	2186
rs782799539	snp	C/T	1.67273e-05	0.00289195	intron-variant	BPTF	GRCh38.p7	17:67946375	GCTTGAATTATTGTG[C/T]TGTGCAGTAGAATTA	2186
rs782800741	snp	A/G	3.33907e-05	0.00408586	intron-variant	BPTF	GRCh38.p7	17:67948053	AATGAAACGCCCAGC[A/G]TTACATAGGTTGTGT	2186
rs782801015	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67974793	CTGGGCACACCACCT[A/G]ACAGTTGCCTCCACA	2186
rs782807609	in-del	-/TTTTTTTTTTTTTTTTTTTT			downstream-variant-500B	BPTF	GRCh38.p7	17:67984630	TGAAAAACATACTTC[-/TTTTTTTTTTTTTTTTTTTT]TTTTTTTTTTTTTTT	2186
rs782808064	in-del	-/A			intron-variant	BPTF	GRCh38.p7	17:67973883	ATTCTTATACTAGAT[-/A]ACAGTTAAATCTGTT	2186
rs782811761	snp	C/G	1.64741e-05	0.00286998	missense	BPTF	GRCh38.p7	17:67945835	CCTCACAACCGATTC[C/G]AATTCAACCACATAC	2186
rs782813608	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67950636	TGAGGTCAGGAGTTC[C/G]AGACCATCCTGATCA	2186
rs782814769	snp	A/T			intron-variant	BPTF	GRCh38.p7	17:67981265	AGATTTAAGGCAGAA[A/T]GAAACATAACTAGCC	2186
rs782815100	snp	A/G	1.65343e-05	0.00287521	synonymous-codon	BPTF	GRCh38.p7	17:67959747	TGCTTCCCAGAAGAG[A/G]AAGCGGGAAGAGGAA	2186
rs782818928	snp	A/C	1.64743e-05	0.00287	intron-variant, missense	BPTF	GRCh38.p7	17:67946078	TTGTGGCTCAGATAC[A/C]GGCTCAGCAAAGTGG	2186
rs782819436	snp	C/T	1.70284e-05	0.00291786	intron-variant	BPTF	GRCh38.p7	17:67964167	TATTATAAGTAACAT[C/T]ATCCCATGTGTTTTG	2186
rs796091334	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67871969	TAGCTGGGATTACAG[A/G]CGTGTGCCACCACAC	2186
rs796101861	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67848386	GTCAACAAATGAGCC[A/G]GGGGGCATGAGTAAT	2186
rs796115403	in-del	-/CT			intron-variant	BPTF	GRCh38.p7	17:67909279	CAGGTCCCCCCCCCC[-/CT]TTTTTTTTTTATCCT	2186
rs796139269	in-del	-/G			intron-variant	BPTF	GRCh38.p7	17:67931035	ACTTTGGGAAGCCAA[-/G]GGGGGCGGATCACAA	2186
rs796194588	in-del	-/ATTTGAGAGAAGC			intron-variant	BPTF	GRCh38.p7	17:67914929	AATTTGCCAAAACAT[-/ATTTGAGAGAAGC]ATTTGAGAGAAGCAT	2186
rs796218847	snp	C/T			intron-variant, downstream-variant-500B	BPTF	GRCh38.p7	17:67929786	GCACTAGACCACCCA[C/T]GGAAGTGTGCTGTGC	2186
rs796243310	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67917140	ATTGTCCTTTTTTTT[C/T]TTTTTTTTTTGAGAT	2186
rs796246385	in-del	A/GGAATATTTTGTCAGTCTTTAGTATCAG			intron-variant	BPTF	GRCh38.p7	17:67879041	AGTCTTTAGTATCAG[A/GGAATATTTTGTCAGTCTTTAGTATCAG]AATATTTTGGCCTCA	2186
rs796252385	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67936645	TGTATGATGAACTAC[C/T]CAACCCTGCCGCCTG	2186
rs796256448	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67836783	CACACTTCTTAAAGT[C/T]TTATTCAGTAAGTTA	2186
rs796273903	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67848183	ATTCTTTTTTTTTTT[-/T]GAATTAGTACAATAA	2186
rs796371334	snp	C/T			upstream-variant-2KB	BPTF	GRCh38.p7	17:67823678	TTGTCACCCTTAGAG[C/T]TCGACCAAATTGTAT	2186
rs796392052	multinucleotide-polymorphism	CA/TG			intron-variant	BPTF	GRCh38.p7	17:67859046	TTGAGCACTTCATGT[CA/TG]GCCTCACAGTGTCCT	2186
rs796413260	in-del	C/TT			intron-variant	BPTF	GRCh38.p7	17:67884146	TTCTTTCTTTTTTTT[C/TT]TTTTTTTTTGAAACA	2186
rs796413398	multinucleotide-polymorphism	ATG/GTA			intron-variant	BPTF	GRCh38.p7	17:67846070	TTCTTGAATATAGGG[ATG/GTA]CATTCACTAGTGGTT	2186
rs796459965	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67872953	TTAGCCAGGCGTGGT[A/G]ACACATACCTATAGT	2186
rs796471027	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67909279	CAGGTCCCCCCCCCC[C/T]TTTTTTTTTTTATCC	2186
rs796507582	in-del	-/GT			intron-variant	BPTF	GRCh38.p7	17:67878702	TGTGTGTGTGTGTGT[-/GT]CAGTCGTTTAGATAT	2186
rs796512894	in-del	-/AC			intron-variant	BPTF	GRCh38.p7	17:67880959	ATATTATATATATAT[-/AC]ACACACACACACACA	2186
rs796524606	in-del	A/TT			intron-variant	BPTF	GRCh38.p7	17:67839334	TCCTAAGTTTTTTTT[A/TT]AAAAAAAATCAGCTA	2186
rs796547669	in-del	-/CTT			intron-variant	BPTF	GRCh38.p7	17:67909279	CAGGTCCCCCCCCCC[-/CTT]TTTTTTTTTATCCTG	2186
rs796585770	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67858632	GATGCTGCCTGTCAG[A/G]GAGCCCGGTGCTTGT	2186
rs796586941	multinucleotide-polymorphism	CC/TT			intron-variant	BPTF	GRCh38.p7	17:67917136	GGTATTGTCCTTTTT[CC/TT]TTTTTTTTTTTTGAG	2186
rs796602094	snp	A/G			intron-variant	BPTF	GRCh38.p7	17:67836462	ATTTCAGAAATGCAT[A/G]TATTAATCTGTGTGG	2186
rs796661241	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67851067	CTATGGAGGATTCAT[C/T]ACCAGACTGGGAAGC	2186
rs796670186	in-del	-/A			intron-variant	BPTF	GRCh38.p7	17:67866000	TGGCACATGTCTGTA[-/A]GTCCTAACTACTTGG	2186
rs796685157	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67880790	TATAGGCTAATTATC[-/T]TTTTTTTTTCTAGTT	2186
rs796685159	in-del	-/G			intron-variant	BPTF	GRCh38.p7	17:67904250	GCCAGGTGAGTCTTG[-/G]AACTCCTGACCTCAG	2186
rs796706461	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67838484	TGTGTATGTACATAC[-/T]TTTTTTTTTTGAGCT	2186
rs796711763	in-del	CCGGT/TG			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67896468	GAGTAACTAGAAACT[CCGGT/TG]CCCCCCAGTGCACAT	2186
rs796719106	snp	C/G			intron-variant	BPTF	GRCh38.p7	17:67907692	AGTTGTCACTGACCA[C/G]TTTTTTTAATCCTGC	2186
rs796784982	in-del	CCGGTTC/TGT			intron-variant, upstream-variant-2KB	BPTF	GRCh38.p7	17:67896468	GAGTAACTAGAAACT[CCGGTTC/TGT]CCCCCAGTGCACATA	2186
rs796792808	in-del	-/A			intron-variant	BPTF	GRCh38.p7	17:67845169	TTCCATTATTGATAT[-/A]GATCACTTGGTAAAG	2186
rs796811508	snp	C/T			intron-variant	BPTF	GRCh38.p7	17:67902395	CTGGCATAGTCACCC[C/T]GCCTTACTCCTGTAG	2186
rs796889971	in-del	-/TTCCTTTC			intron-variant	BPTF	GRCh38.p7	17:67917133	TATGGTATTGTCCTT[-/TTCCTTTC]TTTTTTTTTTTTTTT	2186
rs796903648	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67861341	TTCCAAGATTTTTTC[-/T]TTTTTTTTTTTTTTT	2186
rs796905318	in-del	C/TT			intron-variant	BPTF	GRCh38.p7	17:67884422	CCCTGGCCCCTCCCT[C/TT]TTTTTTTTTCTGACA	2186
rs796935926	in-del	G/TT			intron-variant	BPTF	GRCh38.p7	17:67879144	TTATTTCTTTTTTTT[G/TT]TTTTTTTCTTTTTGA	2186
rs796959613	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67832056	ACCACGCCCGTCTAA[-/T]TTTTTGTATTTTTAG	2186
rs796963567	in-del	-/G			intron-variant	BPTF	GRCh38.p7	17:67931034	ACTTTGGGAAGCCAA[-/G]GGGGGGCGGATCACA	2186
rs796964349	in-del	-/TTTT			intron-variant	BPTF	GRCh38.p7	17:67895965	AGTACTCAATCAGGC[-/TTTT]TTTTTTTTTTTTTGA	2186
rs796966602	in-del	-/T			intron-variant	BPTF	GRCh38.p7	17:67884433	TCCCTTTTTTTTTTT[-/T]CTGACAAGTTCTCAC	2186
rs796982263	in-del	-/A			intron-variant	BPTF	GRCh38.p7	17:67937393	TGTCAAAAAAAAAAA[-/A]GAAAGAAAAGTACTT	2186
rs11552205	snp	C/T	0	0				:	CGTGTTAACCTAACA[C/T]AAAACACAGCAAGAA	2186
rs200305755	snp	C/T						:	AATCATGGGTTTTCG[C/T]AGAAGATTTACATAG	2186
rs201274897	snp	A/G						:	GTATCACTGCATTGT[A/G]GTAATAGCTTCTATA	2186

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