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

NFX1

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs185348872	snp	A/G	0.00279162	0.0372561	intron-variant	NFX1	GRCh38.p7	9:33359472	GGCATGGTGGCAGAC[A/G]CCTGTAGTCCCAGCT	4799
rs185376845	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33306316	AAAAGGGAGGAGTTA[C/T]AGAGGGAAGATGTGA	4799
rs185384893	snp	C/T	0.00179819	0.0299309	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352738	AGTGTTACTTAAATG[C/T]TAACAACTGATGGCC	4799
rs185449474	snp	A/C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33299997	TTTCTAGTTGTGTGA[A/C/T]CTTGGATAAATGATC	4799
rs185460094	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33347394	CAAATATCCTTCATG[C/T]CCCTGTATACTCAAT	4799
rs185479042	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33331859	GTGACTGACTTCCTT[C/T]CCACACACCATCATC	4799
rs185483059	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33307484	TTGAATCCTTACCAC[A/T]GCCCAGTAATAGATA	4799
rs185488640	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33296137	TCACCATGTTGGCCA[C/G]GCTAGTCTCAAACTT	4799
rs185495156	snp	A/C	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33353780	TGCAACCTGCACCTC[A/C]CAGGTTCAAGTGATT	4799
rs185498204	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33370201	TTGTATGGTCACTAG[A/G]TATGCAATCACGCAT	4799
rs185511810	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33329707	TCCATCACCCAGGAT[A/G]GAGTGCAGAGGCGCA	4799
rs185523531	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33368999	GAAACTGCCAGAGTC[A/G]GGTCCAGTCCTGCTT	4799
rs185532901	snp	A/C	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33300959	GATCCTGTATTGCCC[A/C]GTGGATCCTCAGGCT	4799
rs185739755	snp	G/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33309848	TATATAGCCAGTGTT[G/T]TGGACCTCTGGTCTA	4799
rs185799638	snp	C/T	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33362068	GGAAGTTACAGTGAG[C/T]TGAGATCATGCCACT	4799
rs185806785	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33355006	GCTGCGTCTTTTACC[A/G]TTATCAAAGAGCAAG	4799
rs185866251	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33337480	GTACACCCATCTACT[A/G]AGATGAGCATGGCTT	4799
rs185964527	snp	C/T	0.0023933	0.0345097	intron-variant	NFX1	GRCh38.p7	9:33362338	TTGCAGCACTATTTA[C/T]AATAGCCAAGATATG	4799
rs186001542	snp	C/T	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33358994	GTGAGCCACCACACC[C/T]GGCCTAAATTGGTAT	4799
rs186044438	snp	C/T	1.65965e-05	0.00288062	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33338560	AAACGGTTGTGTGGA[C/T]GGCATAAATGTAATG	4799
rs186044646	snp	A/C	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33314039	CCCAGGCTGGAGTGC[A/C]GTGGCGTGATCCTAG	4799
rs186060947	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33359310	GTGGTAATAATAGAT[A/G]TTCCTTGGCCGGGCG	4799
rs186075116	snp	A/G	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33292707	ATATCCTGTATATGA[A/G]TACATGCAGCCTTCT	4799
rs186096975	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33320717	AGTGGGTGTTGAAAG[C/G]CCATGCATTTAGAAA	4799
rs186101318	snp	A/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33341975	ACAAAACTTACCTGG[A/T]CATTGTTGTGGGCAC	4799
rs186204314	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33315934	ACAACAATGCCAGTC[C/T]TTTTGTGGGATCCAC	4799
rs186208753	snp	C/T	0.000798403	0.0199641	intron-variant, utr-variant-3-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33347886	TCACAGCAACCTGGA[C/T]GGATTTGGAGACCAT	4799
rs186281307	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33344293	ATGCTGTGATGGCTG[C/G]CCCTTGCTCCCGGCT	4799
rs186344179	snp	C/T			upstream-variant-2KB	NFX1	GRCh38.p7	9:33288918	TTTGAAGACCATCCC[C/T]CTGATGGGACCAGCA	4799
rs186352949	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33325992	CTATAACCTGTAGAA[A/G]TATATTTGATAATTA	4799
rs186360022	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33365554	TCAAGCCTGCAGTAA[A/G]CTGAGGTTGAGTCAC	4799
rs186618186	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33329554	CAAGCACAAAGGCCA[C/G]ACTCTCTTTAAGTAA	4799
rs186619775	snp	A/G	0.00199481	0.0315187	intron-variant	NFX1	GRCh38.p7	9:33305365	TAGCATAGGCAGTTC[A/G]AAATCAACAGGGTTT	4799
rs186630413	snp	A/C	0.00159617	0.0282053	intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33351375	TGAGATGGGAGGATC[A/C]CCTGAGCCCCAGGAA	4799
rs186633518	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33368507	GAAACCAGAATTGTG[C/G]GCTGAAACCAACTTT	4799
rs186654554	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33294108	CCCCTGAACTGTTAG[C/T]TGGCCTTAAATTTTT	4799
rs186668495	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33333754	AAGAGAAGAGTGGCC[A/G]TTTGGGAGGTACCCA	4799
rs186670098	snp	C/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33355499	TTTGTGACATTCACT[C/G]CTGTTGTTGCATGTA	4799
rs186676235	snp	A/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33342989	CAATATGTTGAGACT[A/T]TTTTTAAAGTTACTT	4799
rs186686808	snp	A/G	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33324578	AACTTCATTAAAGGG[A/G]CTCAATAGTAGATTT	4799
rs186872727	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33321052	TGATATGGAGATCAA[A/G]TGACTAGTAAATCAA	4799
rs186887143	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33304241	CACTCCAGCCTGGGC[A/G]ACAGAGTGAGACTCC	4799
rs186892448	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33328449	GGAAGAAGCATTGAC[A/T]GCATACTTCCCTCAA	4799
rs187016901	snp	A/C	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33307722	TCTGTCTGGGGAAAG[A/C]CAATTGTTTAGGGTC	4799
rs187055951	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33354548	AGCAGCCAGGGAACA[C/T]TCTGAGGCCACTGGA	4799
rs187234823	snp	C/T	0.00279162	0.0372561	intron-variant	NFX1	GRCh38.p7	9:33332268	TTCATGAAAAGTCTG[C/T]AAGCCTGGAGTCCTC	4799
rs187248802	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33370661	CTGGCACTTCTCATA[C/G]CACATCACTGAACCT	4799
rs187310177	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33308655	CTGCATCTGTAAAAT[A/G]ATAATGATAGTAATA	4799
rs187516450	snp	C/T			upstream-variant-2KB	NFX1	GRCh38.p7	9:33290410	CCTGGCGCGTCTATC[C/T]GACGTCACGAACGCG	4799
rs187534353	snp	A/T	0.00013187	0.00811895	intron-variant	NFX1	GRCh38.p7	9:33318690	ATTTTAAGAACCCAT[A/T]CATGTTACTAACGTT	4799
rs187537841	snp	C/T	0.00318978	0.0398085	intron-variant	NFX1	GRCh38.p7	9:33339735	GGTCCAATGGGAGTA[C/T]AGGCATTGGGTATAT	4799
rs187539417	snp	A/G	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33361204	TGGGAACATAATTAG[A/G]AGACTATGAGCCATG	4799
rs187546570	snp	C/T	0.0130921	0.0798413	upstream-variant-2KB	NFX1	GRCh38.p7	9:33289998	TGAGAATAAACGCCT[C/T]TGTAAAAAAAAAAAA	4799
rs187555366	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33339671	CAAGACAAGGCAAGT[C/T]GCTTTGCCTATGAGC	4799
rs187566952	snp	C/T	0.00279162	0.0372561	intron-variant	NFX1	GRCh38.p7	9:33313073	CATGATAGCTGTCCT[C/T]CCGTCTGTAAAGTAC	4799
rs187632547	snp	C/G/T			intron-variant	NFX1	GRCh38.p7	9:33364279	CTTCTCTTGGTTTCT[C/G/T]GAAACTGTCCCCTTA	4799
rs187741977	snp	C/T	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33297119	TCTTCTCACAGCTCC[C/T]CCTCTCCTTACTGCA	4799
rs187756290	snp	A/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33322895	GTTCATCAGAGAGAA[A/T]CAGGGAAAGGTAGCT	4799
rs187772780	snp	A/G	0.00398564	0.0444627	intron-variant	NFX1	GRCh38.p7	9:33345023	AAAAGTTAGCCAGGC[A/G]TTGTGGCGGGCACCT	4799
rs187779032	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33362760	CCAGGCTGTAGTGCA[A/G]TGGCGCTATCTCAGC	4799
rs187812943	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33316593	TAGTTATCTAGCAGA[A/G]TATTTTGGCCATGTA	4799
rs187819390	snp	C/G	0.00517822	0.0506191	intron-variant	NFX1	GRCh38.p7	9:33360677	TATGTGTGTATATCT[C/G]TATTGTAGAAATAAA	4799
rs187872402	snp	C/T			intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33350509	CTAGTTACCTAGTTA[C/T]ATTTGTTTGTTGTCA	4799
rs187877639	snp	C/T	0.00279162	0.0372561	intron-variant	NFX1	GRCh38.p7	9:33309173	CCATCCTGGCTAAGA[C/T]GGTGCAACCCTGTCT	4799
rs187908075	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33346205	CAGGCCAGTCCCCAC[C/T]GATTGCCTCCTTTAC	4799
rs188105222	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33370393	ATCAGACAGACATTG[C/T]TTGCTTTACCCAAAC	4799
rs188126574	snp	C/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33292308	AGCATCATCTTTAGC[C/G]CACACCCTCATCATC	4799
rs188161527	snp	A/G	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33368249	CTCAAAAAAAAAAGA[A/G]TAGTTACTCTGAAGA	4799
rs188169223	snp	A/C	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33298475	ATGTCATGAACTTAC[A/C]TTCTAAAATAATCAC	4799
rs188327495	snp	A/G	0.00318978	0.0398085	intron-variant	NFX1	GRCh38.p7	9:33297380	AACCTCAATGTATAT[A/G]TGAAGCAAAGCAATG	4799
rs188337843	snp	A/G	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33345272	ACCTGAGGTCAGGAG[A/G]TTGAGACCAGTCTGG	4799
rs188341712	snp	C/T	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33358172	TTCTGTTTCCCAGGC[C/T]GGAGTGCAATGGTGT	4799
rs188385786	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33327271	CTCAAGCAGTCCTCC[C/T]ACCTTGGCTTCTCAA	4799
rs188400071	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33367054	TTCTTCAGGCAAGGG[A/G]GCCTGCCCATCATAT	4799
rs188603306	snp	C/T	0.0119091	0.0762411	intron-variant	NFX1	GRCh38.p7	9:33323703	GGTTGCAGTGAGCCG[C/T]GATTGCGCCACTGCA	4799
rs188623131	snp	C/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33363317	TTAGACAGAGTCTCA[C/T]TGTGTTGCCCAGGCT	4799
rs188655768	snp	A/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33310227	TTTTACAGCAAATTC[A/T]GTTACCCATCTGATT	4799
rs188668664	snp	A/G	0.0023933	0.0345097	intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33349781	GGAGACATGAGGAGA[A/G]TTAAGTATTTAATTA	4799
rs188789547	snp	C/T	0.00318978	0.0398085	intron-variant	NFX1	GRCh38.p7	9:33330953	GGAGGCTGAGGTGGG[C/T]GGATCATGAGGTCAG	4799
rs188791877	snp	A/G	0.00557542	0.0525036	intron-variant	NFX1	GRCh38.p7	9:33361372	GCATGATGTGTATGT[A/G]TACATTGTGGAATGG	4799
rs188793854	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33306733	GCCGACTTTATAGTT[C/G]TGGAATAGGTGAGTT	4799
rs188799758	snp	C/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352974	GGTCTCGCCCTGTTT[C/G]CCAGGCTGGTCTCCC	4799
rs188816516	snp	A/G	0.00358779	0.0422022	intron-variant	NFX1	GRCh38.p7	9:33369676	GTAAATAGAGAATTT[A/G]TTATCTCACAGAATA	4799
rs188854254	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33303723	TGGCATCTTCCCTCT[G/T]TATGGAATACTTCTT	4799
rs188881387	snp	G/T	0.0023933	0.0345097	intron-variant	NFX1	GRCh38.p7	9:33356532	CCAGTTTATTTGAGT[G/T]TCTTAATAAGCACTT	4799
rs188980669	snp	C/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33292991	GCCCTCCATCCCATC[C/T]CCTAGAATTCTGCCT	4799
rs188986523	snp	A/T	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33320769	AGATTGAATAGGAAA[A/T]TTATTTCTAAAACTA	4799
rs189000878	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33342000	GGGCACCTGTAATCC[C/T]AGCTACTCAGGAGGC	4799
rs189005892	snp	C/T	0.0189856	0.0955633	intron-variant	NFX1	GRCh38.p7	9:33361993	CCGGGCATGGTGGCA[C/T]ACTTGTAGTGCCAGC	4799
rs189043089	snp	A/G	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33335723	ACTCAGTCCTCCCCC[A/G]GGTAACCACTGATCT	4799
rs189043173	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33311635	TCGGCTCACTGCAAC[C/T]TCTGCTGCCTGGGTT	4799
rs189057417	snp	C/T	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33357271	GGTGCCACTGCACTC[C/T]AGCCTGGGCGACAGT	4799
rs189155413	snp	C/T	0.00199481	0.0315187	intron-variant	NFX1	GRCh38.p7	9:33341693	TCCACTTTTTGAGGC[C/T]GAGGTGGGTGGATCT	4799
rs189223668	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33337186	TCCATATCCATGGGT[C/T]CCATATCCATGGATT	4799
rs189425692	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33324995	TATAATGAAGAGAAA[G/T]GAACAAAGCCTCAGA	4799
rs189430140	snp	A/G	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33298837	GGCTCTAAGAAGGCA[A/G]CAGGACAAGTTAGGA	4799
rs189440108	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33320587	ACTTGAATATAGAAA[C/G]CAGAAAAAGCTCATT	4799
rs189451953	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33364465	TTGGAGCTATAACAG[C/T]TCTTATTTTTCTCCT	4799
rs189453303	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33361554	GAGGCGGGTGGATCA[C/T]CTGAGGTCAGGAGTT	4799
rs189463074	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33319316	CCCATACATTTGCCC[A/G]AATGATCTCTCTGAT	4799
rs189493456	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33312103	TGAGGCCCAGTAAGA[A/T]CTTAAAATGATTTTT	4799
rs189651145	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33296412	TCACTCAGTTCGCTG[A/G]CGAAGTCTTACTCAT	4799
rs189659275	snp	C/T	1.78039e-05	0.00298356	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33354099	AGAATAGCTGCAATC[C/T]CCATGGCCTCTAAGA	4799
rs189674181	snp	A/C	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33322518	AAATTCTGGTGAGTG[A/C]AGCTGAGCAGTTAGG	4799
rs189681001	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33344374	ATCACAGTGCCCTCC[A/G]TTGGTTTACTCTAGG	4799
rs189742286	snp	A/G	0.00279162	0.0372561	intron-variant	NFX1	GRCh38.p7	9:33291130	CCCTGTACTGTACCT[A/G]TTCTGTAATTGTTCA	4799
rs189902170	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33301723	ATTTCCTGTGGATAC[A/G]TAAACAGAAGTGTGA	4799
rs189910567	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33326495	AGGCTGAGGTGGAAG[C/G]ATCACTTGAGGCTAG	4799
rs189945512	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33340632	TTTCTCTCACATTGT[C/T]AGGCTGCAAATTTTC	4799
rs189972059	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33300012	CCTTGGATAAATGAT[C/T]TAACTACATGAAGCC	4799
rs189984743	snp	A/G	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33347516	CCTGCAAGAATGGCA[A/G]TAATCAAAAAATAAT	4799
rs190036207	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33329773	AAGTGATTCTTATGC[C/T]TTAGCCTCTGGAGTA	4799
rs190051061	snp	A/G	0.00318978	0.0398085	intron-variant	NFX1	GRCh38.p7	9:33369127	CTGGAGTGCAGTGGC[A/G]CGATCTCAGCTCACT	4799
rs190053757	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33365145	TGGGTGTGGTGGCGG[A/G]CACCTGTTATTCCAG	4799
rs190236607	snp	A/G	0.00358779	0.0422022	intron-variant	NFX1	GRCh38.p7	9:33325596	ATGAACCCGGGAGGC[A/G]TAGCTTGCAGTGAGC	4799
rs190260501	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33333489	TGCAGCTTCACACAT[C/T]GGGTCTCTGCCCAAC	4799
rs190262275	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33309126	ACTTTGGGAGGCCAA[A/G]GCGGGTGGATCACGA	4799
rs190266539	snp	C/T	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33306374	AGGTGACTGTGAAAC[C/T]CCAAGCAAGAATGTT	4799
rs190277332	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33355007	CTGCGTCTTTTACCG[C/T]TATCAAAGAGCAAGA	4799
rs190293221	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352784	CATGTGTTTTGTTTT[A/G]TTTTTAAAGCTAGTC	4799
rs190314212	snp	C/T	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33314062	GATCCTAGCTCACTG[C/T]AACCTCCACCTCCCA	4799
rs190319746	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33338741	CATAGTCCCCATAAC[C/T]TCTCTGCAAAGAGAC	4799
rs190323400	snp	A/G	0.00398564	0.0444627	intron-variant	NFX1	GRCh38.p7	9:33359321	AGATATTCCTTGGCC[A/G]GGCGCGGTGGCTCAC	4799
rs190504316	snp	C/T	0.00318978	0.0398085	intron-variant	NFX1	GRCh38.p7	9:33313368	CTGAGGCAGGAGGAT[C/T]GCTTAAGCCTAGGAG	4799
rs190525696	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33359246	CTTTTATTTCTTCTT[C/G]TTACCTCATTGTATT	4799
rs190771544	snp	A/G	0.00557542	0.0525036	intron-variant	NFX1	GRCh38.p7	9:33337916	TAGCCGGGCGTGGTG[A/G]CGCACACCTGTAATC	4799
rs190782328	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33307618	TGCTGCTTCCATTAC[A/G]TTACACTGCTTGCTT	4799
rs190862630	snp	C/G	0.00358779	0.0422022	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33365748	GACACTCTAGCCCCT[C/G]AGATCTTTGAAGGGC	4799
rs190862876	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	NFX1	GRCh38.p7	9:33289579	TTGTGCCTTACCTCA[A/G]GAGCCACCCGTTCCC	4799
rs190866831	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33339462	AATTACCTCCCACCA[A/G]GTCCCTCCCACAACA	4799
rs190872550	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33362637	AAGGGAGGTTGAGGA[A/G]AGGTTGGTCAGTGGA	4799
rs190938632	snp	A/G	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33345031	GCCAGGCATTGTGGC[A/G]GGCACCTGTAATCTC	4799
rs190950269	snp	C/G	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33363059	TAACGGTAAGGTGTA[C/G]TATTTTACAAAATAG	4799
rs191107627	snp	A/G	0.00517822	0.0506191	intron-variant	NFX1	GRCh38.p7	9:33316309	CCTGGTACTTACCAA[A/G]CCTTTTTTTTTTTTT	4799
rs191128529	snp	A/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33298793	TGTCTCAAAAAAAAA[A/T]ATATTATTAAGCTGC	4799
rs191144858	snp	A/G	0.0185938	0.0946107	intron-variant	NFX1	GRCh38.p7	9:33324703	GAGGCTGAGGCAGGC[A/G]AATCACGAGGTCAGG	4799
rs191149095	snp	A/C	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33346496	CATGAAGATGGGCTA[A/C]ATAATGTGGCAGCAA	4799
rs191153028	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33364308	TAAAGAACTGAACTT[G/T]GGGTAGGGTTGAGAT	4799
rs191177785	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33327117	GAAAACTAAAAAAGA[C/T]GAACATAAATCCAGC	4799
rs191196820	snp	A/T	0.00119737	0.0244387	intron-variant, downstream-variant-500B	NFX1, LOC105376018	GRCh38.p7	9:33349146	GACTTCATTCAACAG[A/T]TATCGAGTATGAGTA	4799
rs191197032	snp	A/T	0.000798403	0.0199641	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33366257	AAAGTAGAACATACT[A/T]TTAAAGGAAATAATA	4799
rs191315388	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33321060	AGATCAAATGACTAG[C/T]AAATCAAATCCCCTT	4799
rs191330333	snp	C/T	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33359745	TCAACAACTGACAAA[C/T]TTTCTGATTCTAGCA	4799
rs191333895	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33362174	TTACACATTCTTGGT[A/G]GGATTGTAAATTAGT	4799
rs191372190	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33304308	AAATCACCAATGACT[C/G]CTTTCCAGCCATATC	4799
rs191395806	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33303929	CCTCCCTGAAGCATT[A/G]CATTTTTGCTTCTGT	4799
rs191413963	snp	A/G			intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33350122	CAGCCTGGCCAACAT[A/G]GTGAAACCCTGTCTC	4799
rs191554656	snp	A/G	3.29598e-05	0.00405941	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33295197	AACAGGAGGGCCACC[A/G]ACATACAAACGCAGG	4799
rs191570755	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33343129	GTGTTATTGACCTAG[G/T]TTCTGTCCTCAACAA	4799
rs191580555	snp	C/G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33329224	AAGTATTACTCTCTC[C/G/T]GCTTCAGTGTGTGCC	4799
rs191590753	snp	A/T	0.000798403	0.0199641	intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33350855	TAATAATCCTTATTT[A/T]AAAAACTGAGCTGAG	4799
rs191609181	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33368469	AGCTCTGAGAGTTGG[C/G]TGACTGTTGGGCTTT	4799
rs191662830	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33332858	ACTTTTTTTCTTTTT[C/T]CTTTTGAGACGGAGT	4799
rs191666376	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33327695	ATAGTCAAAGATACA[A/G]TGAGGCTGAAAGTTA	4799
rs191681244	snp	C/T	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33367110	GTTCCTCTGTCTGTC[C/T]TCTCCTTGGCTCTGT	4799
rs191687312	snp	A/G	0.000798403	0.0199641	downstream-variant-500B	NFX1	GRCh38.p7	9:33371232	TCCTCCTCCTGTAGC[A/G]GGGCTGTCCTTTGGT	4799
rs191785790	snp	A/G	0.00199481	0.0315187	intron-variant	NFX1	GRCh38.p7	9:33335935	TTTATCCATTCACTG[A/G]TTGATGGATATTAGA	4799
rs191791284	snp	C/G	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33357280	GCACTCTAGCCTGGG[C/G]GACAGTGGGAGACTC	4799
rs191943190	snp	A/G	0.0023933	0.0345097	intron-variant	NFX1	GRCh38.p7	9:33308315	GCTGTGGTGGCACAC[A/G]CCTGTAGTCCCAGCT	4799
rs191951590	snp	C/T	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33311672	ATTCTCCTGCCTCAG[C/T]CTCCCAAGTAGCTGG	4799
rs191988283	snp	A/G	1.6525e-05	0.00287441	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33290582	CACGGGATGGCGGAG[A/G]CGCCTCCTGTCTCAG	4799
rs192010198	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33340317	CCAAGGTTTGGTGCC[C/T]GCACTCTGAAGCCTT	4799
rs192014623	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33361213	AATTAGAAGACTATG[A/G]GCCATGAAGACAGTT	4799
rs192161172	snp	C/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33309737	GGCTCAAGCGATCCT[C/T]CCACCTCAGCCTCCC	4799
rs192178287	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33356040	TAGGGTTTATGTGTG[C/T]TCAGCATTAGTAGAT	4799
rs192250289	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33323376	TGCAAAGAAACAGGG[A/G]AAAAAACAGGCAACA	4799
rs192256742	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33297281	GTGAGATACAGCCCA[A/G]CCCTTGAAGCCACCA	4799
rs192444274	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33310254	GATTAATTAGTCTTG[A/G]CTCTGATTGGCTTTT	4799
rs192452288	snp	A/G	0.0103295	0.0711199	intron-variant	NFX1	GRCh38.p7	9:33302805	CTCCTGAGTAGCTGG[A/G]ATTACAGGCGCGCAC	4799
rs192495347	snp	C/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33368867	CTCAGCCAAGAGCGT[C/T]CTGGTCCCCAGGACC	4799
rs192561675	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33333955	TTCAAGGCCAGCCTA[A/G]CCAACATGGTGAAAC	4799
rs192643345	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33291938	ACACTGCATTGGTGT[A/G]CCCTAGTCTTGATGT	4799
rs192655008	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	NFX1	GRCh38.p7	9:33290374	TCCATCCAGCTACTA[C/G]TCTCCTCCTCCCGCC	4799
rs192656591	snp	C/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33341145	GAGACATATCCAAGA[C/T]TGGGCAAGTTACAAA	4799
rs192668811	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33317701	TTAATTATGGCCGGG[C/T]GTGGTGGCTCACGCC	4799
rs192699649	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352157	ACATGGTTCCTCACA[A/G]TCTGATAGGACAGAT	4799
rs192795335	snp	A/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33323880	AGAATATTGATAAAG[A/T]GATAGAAACTAGTTT	4799
rs192802765	snp	G/T	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33363936	AGAATTTAGGATATA[G/T]TAGGCACTCGGGGTT	4799
rs192872994	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33319351	GTATTTTATTGTTAA[C/T]TCTGGACAACTGTGG	4799
rs192882524	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33361427	CATTACCTCACATTC[C/T]TATTTTTGGGGGGGT	4799
rs192997787	snp	C/T	0.00636936	0.0560724	intron-variant	NFX1	GRCh38.p7	9:33297939	AATCTGGAAGACCAT[C/T]TTAGAATTCTATTTA	4799
rs193051141	snp	C/T	0.00318978	0.0398085	intron-variant	NFX1	GRCh38.p7	9:33369352	ACAGGCGTGAGCCAC[C/T]ACACCTGGCCATCCC	4799
rs193063836	snp	C/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33335412	ATTTTTTTGTATTTT[C/T]AGTAGAGACGGGGTT	4799
rs193148986	snp	A/T	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33360692	CTATTGTAGAAATAA[A/T]AACCTAGCAGGCCAA	4799
rs193151313	snp	C/T	0.00676609	0.0577691	intron-variant	NFX1	GRCh38.p7	9:33329667	TTTTTTAATTTTATT[C/T]ATTTATTTTGAGACA	4799
rs193235091	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33356608	ATATTCTGTTATTAT[C/G]TAGAAACTGTGTTAT	4799
rs193295583	snp	A/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33339711	CAAAAGCAAATTAGT[A/T]ACTTCCTAGGTCCAA	4799
rs193299009	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33305482	GGGCTGACCCTTTGA[C/T]ACCAGTCTCAGATGT	4799
rs199530688	snp	A/C	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33304796	TACTACCAGAAAGGC[A/C]GCATGAAACTGGAAG	4799
rs199540118	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33340558	TACATTTGGCTCCTT[G/T]TCACTTATGCAAATT	4799
rs199550083	snp	C/T	0.000348646	0.0131985	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33342824	GAAGAACCTTGTCAT[C/T]GTGGAAACTGCCAGA	4799
rs199573527	snp	A/T	0.000346081	0.0131499	intron-variant	NFX1	GRCh38.p7	9:33303157	TAGCTTTTGGAAGAA[A/T]ATTTATTTGGCCTAC	4799
rs199614941	snp	C/G	1.64898e-05	0.00287135	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352724	ACTTATCAAAGGTTA[C/G]TGTTACTTAAATGTT	4799
rs199653342	in-del	-/TTG	0.0103295	0.0711199	upstream-variant-2KB	NFX1	GRCh38.p7	9:33288657	AGAGTGGGTGGTTTT[-/TTG]TTGTTGTTTTAGATT	4799
rs199696015	in-del	-/C	0.0633504	0.166319	intron-variant, utr-variant-3-prime	NFX1	GRCh38.p7	9:33348173	GCCAACAAGGTGAGA[-/C]CCCCCCCCATCTCTA	4799
rs199708243	snp	A/C	0.130809	0.219758	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33351742	TCACCCGTGTATGGC[A/C]CCCTGCCATACCAGC	4799
rs199710298	in-del	-/GAAAAA			intron-variant	NFX1	GRCh38.p7	9:33345186	AAAGAAAAAGAAAAA[-/GAAAAA]AAAGGCCGGGTGCAG	4799
rs199721362	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33369893	GACTGATCATTCTTT[A/G]TTTGTTTTTCAGGAA	4799
rs199721480	snp	C/T	9.88647e-05	0.00703012	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33318977	TGCCAGCAATGCCCA[C/T]GGCTCCCCCAGCTGG	4799
rs199840084	in-del	-/A	0.00676609	0.0577691	intron-variant	NFX1	GRCh38.p7	9:33302079	CTGTCTCAAACAAAC[-/A]AAAAAAACATTTTTT	4799
rs199929040	snp	A/G	0.00199806	0.0315443	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33294871	TGAGAAGGAAGTTGT[A/G]GGTGCAGATCCCAGG	4799
rs199947127	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33309361	GACTCCGTCTCAGAG[A/G]AAAAAAAAAAAAACT	4799
rs199963322	snp	A/C/G			intron-variant	NFX1	GRCh38.p7	9:33368442	TGTTTTCTCAGACAG[A/C/G]AGCAGGGAAGGAGCT	4799
rs199968250	snp	A/T	0.00029703	0.012183	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33295076	TCTAGAAAAGGAGTA[A/T]TGGATGGGTATGGAG	4799
rs199970242	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33359390	GATCACTTGAGGTCA[A/G]GAGTTCGAGACCAGC	4799
rs199999892	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33345175	TCAAAAAAAGAAAAG[A/G]AAAAGAAAAAGAAAA	4799
rs200008052	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33290618	GTCCCGGCCCGAGCG[A/G]GACTGGGCCCCTTTC	4799
rs200043515	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33364137	TACCTGCTTTCTTAA[A/T]TGTGGCTTGTCAGGG	4799
rs200094650	snp	A/G	6.62789e-05	0.00575631	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294740	AATGAGAAGCACCAT[A/G]TCAGAGTCAAGAAAG	4799
rs200099343	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33302167	CATGATATTTTGATA[A/C]AAGCGTACAATGTGT	4799
rs200113863	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33369506	CAAAATCACCAGCTC[A/C]TGTTTGTCCCACTAT	4799
rs200121431	in-del	-/TT			intron-variant	NFX1	GRCh38.p7	9:33302358	TTCTATCTAACTGTA[-/TT]TTTTTTTTTTTTTTT	4799
rs200123067	in-del	-/A	0.0248432	0.108648	intron-variant	NFX1	GRCh38.p7	9:33336726	CCACACAAGCCTCCC[-/A]AATAGCTGGGACCAC	4799
rs200131309	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33309085	AATCCTGGCTGGGCG[A/C]GGTGGCTCATGCCTG	4799
rs200165112	snp	A/G	0.000510755	0.0159724	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33295208	CACCGACATACAAAC[A/G]CAGGACACAGAAACA	4799
rs200191622	snp	A/G			upstream-variant-2KB	NFX1	GRCh38.p7	9:33288725	ACTCCCCATCCCCCT[A/G]TGCGGGGTGTCATTT	4799
rs200253384	snp	A/T	0.000274221	0.0117062	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33369965	TAATTGACTATTTTG[A/T]CGTCCAGGACTAAGA	4799
rs200261259	snp	C/T	0.000131781	0.00811621	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33301361	AGTTGTCAGAGCTGT[C/T]ACCATGTGTTTCATT	4799
rs200261875	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33368237	GACAGACTCCATCTC[G/T]AAAAAAAAAGAATAG	4799
rs200277743	snp	A/G	0	0	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33295116	ATGAGCAGAGAAGAT[A/G]CCCACAGAAAAGGCC	4799
rs200314855	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33361537	CAGCACTTTGGGAGG[C/T]CGAGGCGGGTGGATC	4799
rs200393697	snp	G/T	0.000119823	0.00773932	intron-variant	NFX1	GRCh38.p7	9:33338607	AAGTGGACTTATTAG[G/T]CATAATCAGATTCCA	4799
rs200408791	snp	C/T	3.29592e-05	0.00405938	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294551	TACAGTTCACCACCT[C/T]CCTGTCACCTTTCCA	4799
rs200409340	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33366823	TAAGCAGGGCAAACT[C/G]GACCCAAGAAGCAGG	4799
rs200457624	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33332507	CAAAAGTGAAGGTAT[A/G]ACTGGGGTGGGGCAT	4799
rs200513804	in-del	-/TAAA	0.101301	0.200969	intron-variant	NFX1	GRCh38.p7	9:33341805	TCATAACCCGGTCTC[-/TAAA]TAAATAAATAGATTT	4799
rs200530506	snp	C/G	0.000230616	0.0107357	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33313690	GGCTGTCTCAGTCCA[C/G]TGTTCTAACCCATGT	4799
rs200644598	snp	A/G	0.00199792	0.0315431	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33344135	TTCCCTGTGGTACTA[A/G]GCCCCCTGAATGTAC	4799
rs200672726	in-del	-/A	0.0252325	0.109451	intron-variant	NFX1	GRCh38.p7	9:33369736	CAAAAGTTAAAAAAA[-/A]TTGCTCACAAAGGGC	4799
rs200673847	in-del	-/T	0.00874735	0.0655527	intron-variant	NFX1	GRCh38.p7	9:33311859	CTCGGTCGGCAAGGA[-/T]TTTTTTTTTAACCTC	4799
rs200728891	snp	A/G	0.000209966	0.010244	intron-variant	NFX1	GRCh38.p7	9:33301229	GTTTTTTGTGTTTGA[A/G]TTAATCTTTTTTGTT	4799
rs200740095	snp	C/T	1.73504e-05	0.00294532	intron-variant	NFX1	GRCh38.p7	9:33363979	TTTCCCTCCCACTCC[C/T]TTTATTTGCATACCT	4799
rs200748278	snp	A/G	0.000165497	0.00909512	intron-variant	NFX1	GRCh38.p7	9:33328692	AGGTAAATCCTAAAC[A/G]ATGCTAGAGTTGTTG	4799
rs200777912	snp	A/G	0.000758	0.0194532	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352623	AGTGTGCTAAAAGTC[A/G]TTCCATGTTCATCTG	4799
rs200779591	in-del	-/GAAAAG			intron-variant	NFX1	GRCh38.p7	9:33345169	TCCATCTCAAAAAAA[-/GAAAAG]AAAAAGAAAAAGAAA	4799
rs200838543	snp	A/G/T	0.000281664	0.0118642	intron-variant	NFX1	GRCh38.p7	9:33367648	GCTGCTTTCCAAGGG[A/G/T]ACCTGTCTGTCCAGA	4799
rs200845703	snp	A/G	5.31957e-05	0.00515704	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33342789	GTGGGAGGAAACTCC[A/G]TTGTGGCCTTCATAG	4799
rs200849911	in-del	-/TTTC			intron-variant	NFX1	GRCh38.p7	9:33307779	CAAGATGTCAATCTT[-/TTTC]TTTCTTTCTTTCTTT	4799
rs200878484	in-del	-/G			intron-variant	NFX1	GRCh38.p7	9:33302688	TTTTGTTTTTTTTTT[-/G]AGAGGGAGTCTCACT	4799
rs200887512	in-del	-/TTTTTTT			intron-variant	NFX1	GRCh38.p7	9:33357706	CTGGCTAAGATTTTC[-/TTTTTTT]TTTTTTTTTCTTTTG	4799
rs200888034	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33309109	ATGCCTGTAATCCCA[A/G]CACTTTGGGAGGCCA	4799
rs200911325	snp	A/G	1.67312e-05	0.00289229	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33364025	GAGATTAGCAGAGGC[A/G]TTTCATATCAGTGAG	4799
rs201001565	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33337751	CAAAACAAAACAAAA[A/C]AAAACAAAAACTGAT	4799
rs201013313	snp	A/G	1.64947e-05	0.00287177	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33295098	GGTATGGAGCCAGAC[A/G]AAATGAGCAGAGAAG	4799
rs201037973	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33314108	CCTGTCTCAGCCTCC[C/T]GAGTAGCTGGGATTA	4799
rs201064944	in-del	-/TT	0.0166325	0.0896639	intron-variant	NFX1	GRCh38.p7	9:33323917	AGGCCCAAATGGAAA[-/TT]CTGAAGTTTAAAAGT	4799
rs201117106	snp	G/T	1.65154e-05	0.00287358	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294915	AAAAAGCAACACAGT[G/T]TGTATACAGCTATGG	4799
rs201175137	snp	G/T	0.000229775	0.0107161	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33364819	TCTCTAAGGCCAGCT[G/T]GATGAAAAAAAAAAA	4799
rs201176604	snp	A/C/T	0.000104717	0.0072353	intron-variant	NFX1	GRCh38.p7	9:33364146	TCTTAATTGTGGCTT[A/C/T]TCAGGGTGTTTGGTC	4799
rs201191593	snp	A/G	1.648e-05	0.0028705	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33313665	ACAGGCACACAGTTC[A/G]CTGTGGTCAGGCTGT	4799
rs201286337	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33354075	TTTTCCCTTTCTTTT[C/T]TATATTTCAGAATAG	4799
rs201302875	snp	A/T	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33329657	TTCTTTTTTTTTTTT[A/T]AATTTTATTTATTTA	4799
rs201330782	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33340166	GCAGAGGTTCTCCAT[C/G]AGAGCCCCACCCCTG	4799
rs201337993	snp	C/T	6.85895e-05	0.00585577	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33369966	AATTGACTATTTTGA[C/T]GTCCAGGACTAAGAA	4799
rs201342989	snp	C/T	4.94197e-05	0.00497066	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33318741	TCAAGTATGCTATTG[C/T]GGCAGCACCTCCCGA	4799
rs201380764	in-del	-/CTGGCAAGCTG	0.0256215	0.110247	intron-variant	NFX1	GRCh38.p7	9:33303446	ACAGCCTTTGTGCTC[-/CTGGCAAGCTG]TTCTGGAGATGGCCA	4799
rs201455785	in-del	-/TATTATTATTAT			intron-variant	NFX1	GRCh38.p7	9:33363264	AATAATAAAGAAATG[-/TATTATTATTAT]TATTATTATTATTAT	4799
rs201534408	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33343495	TCCAGCCTTACACAG[A/G]TAGCCTTACACAGGA	4799
rs201584506	snp	C/T	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33361785	GACAAGAGCAAGACT[C/T]CATCTCCAAAAATAT	4799
rs201605365	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33306820	CGGTGCTCTTCTCTT[A/G]TTCCCTCTCTCTGAT	4799
rs201615358	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33345174	CTCAAAAAAAGAAAA[A/G]AAAAAGAAAAAGAAA	4799
rs201619308	snp	C/T	1.64781e-05	0.00287033	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294578	TCCAGGCAGGTCCCT[C/T]ATGATGAAATCTCTG	4799
rs201668706	in-del	-/AGA	0.0197687	0.0974348	intron-variant	NFX1	GRCh38.p7	9:33326867	ACTGCACAAAAGGGG[-/AGA]AGAATAGAGCTGTGT	4799
rs201693581	snp	A/T	0.00199792	0.0315431	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33319063	TAGTAGTCGGAAAAC[A/T]TGCATGGACCCTGTG	4799
rs201709239	snp	A/G			intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33349675	CAGGCCATTTTTCAA[A/G]AAAAAAAAAAAGAAT	4799
rs201729674	snp	C/G	0.000379847	0.013776	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33354164	CAGCAAGTTAATTAC[C/G]AAAAAGGAAGTTCAT	4799
rs201754699	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33317432	TCCAAAAAAAAAAAA[A/T]AAAGAAAGAAAGAAA	4799
rs201756744	snp	C/T	0.00176461	0.0296512	intron-variant	NFX1	GRCh38.p7	9:33367628	CAGACAAGTAAGATT[C/T]TCCAGCTGCTTTCCA	4799
rs201795462	in-del	-/C	0.0193772	0.0965046	intron-variant	NFX1	GRCh38.p7	9:33324736	TCGAGACCATCCTGG[-/C]CTAACATGGTGAAAC	4799
rs201796076	snp	C/G	0.000103201	0.00718261	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33369969	TGACTATTTTGACGT[C/G]CAGGACTAAGAAGAT	4799
rs201803762	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33309360	AGACTCCGTCTCAGA[A/G]AAAAAAAAAAAAAAC	4799
rs201804395	in-del	-/CA	0.0479149	0.147179	intron-variant	NFX1	GRCh38.p7	9:33333135	ACAGGCATGAGTCAC[-/CA]CACCGGCCTCGATTC	4799
rs201910807	snp	G/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33293962	GGCACGTGATATCCC[G/T]AAGTTCATACAATAA	4799
rs201923459	snp	A/G	0.000502684	0.0158458	intron-variant	NFX1	GRCh38.p7	9:33319174	ATATTATTGTAAATG[A/G]TTGGCAGCAGTGAGT	4799
rs201964590	snp	C/T	0.000188642	0.00971007	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33364756	GGAAATGGAAACCCT[C/T]GTGGAGGCCGTGAAT	4799
rs201966078	in-del	-/C/TTTTTT			intron-variant	NFX1	GRCh38.p7	9:33307797	TTTCTTTCTTTCTTT[-/C/TTTTTT]TTTTTTTTTTTTTTT	4799
rs201981020	snp	A/C/G	6.60092e-05	0.00574464	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33366623	TCATCTTTTCCCTCA[A/C/G]TACAGGGAAAGAATA	4799
rs201985524	snp	A/T	0.00199794	0.0315432	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294541	TAGAAGAAATTACAG[A/T]TCACCACCTCCCTGT	4799
rs202062131	in-del	-/C			intron-variant	NFX1	GRCh38.p7	9:33319965	CTTTTCTTTTCTTTT[-/C]TTTTTTTTTTTTTTG	4799
rs202076649	snp	C/T	1.67874e-05	0.00289714	intron-variant	NFX1	GRCh38.p7	9:33354935	CTCCTTGCCCTTGAG[C/T]TCTGTGAAATTAATG	4799
rs202080067	in-del	-/AT			intron-variant	NFX1	GRCh38.p7	9:33357335	AATAAAGTATATCAA[-/AT]ATATATATATATGTG	4799
rs202149955	snp	C/T	8.23662e-05	0.00641688	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33367576	AGGGAAATGCAGGCA[C/T]GGCCTCCACCACCGA	4799
rs202184189	in-del	-/GGCGTT	0.0337553	0.125452	upstream-variant-2KB	NFX1	GRCh38.p7	9:33289941	TGTAAGGAGAGGAGC[-/GGCGTT]GGCAAATGTGAACCA	4799
rs202190162	in-del	-/G			intron-variant	NFX1	GRCh38.p7	9:33317436	AAAAAAAAAAAAAAA[-/G]AAAGAAAGAAAAGAA	4799
rs367553877	snp	A/C	2.17082e-05	0.00329449	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33351831	GCATTGACTGTAGTT[A/C]TGAGGCTACTAGTGA	4799
rs367606850	snp	C/G	0.000421774	0.0145158	intron-variant	NFX1	GRCh38.p7	9:33367667	TGTCTGTCCAGAAAA[C/G]CTAGCAGGGGCTGAA	4799
rs367655547	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33296368	CTTTGCATGGTGTTG[C/T]ATGTGGCTCCCTCTC	4799
rs367736768	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33312162	ATTTTCGGTGAGGTG[C/T]GTTTGTTTAGCCTTT	4799
rs367737839	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33344759	TAGTCCCAGCTACTC[G/T]GGAGGCTGAGGCAGG	4799
rs367795929	snp	C/G	5.38575e-05	0.00518901	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33364840	AAAAAAAAAAGCAAT[C/G]AAGTCCTGGAAACAC	4799
rs367799723	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33301933	AAAAATTAGCCAGGC[A/G]TGGTGGCGGGCACCT	4799
rs367839744	snp	C/T	1.64754e-05	0.00287009	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33303192	ATTTTTCCTGACAGA[C/T]GGCCAGAGTGGTTGG	4799
rs367853433	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33300979	ATCCTCAGGCTATGT[C/T]ACAAGGGGCATTTGG	4799
rs367898584	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33323037	TCAAAAACAATAGAA[C/T]TGCAATTAATGGATC	4799
rs367908993	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33328331	CACTTGGCCTTTTTT[C/T]GACTTAGGCAAATCG	4799
rs367911923	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33300114	AGTCTCACTCTGGAG[G/T]GCAGTGGTGCAATCT	4799
rs367916272	snp	C/G	3.30737e-05	0.00406642	intron-variant	NFX1	GRCh38.p7	9:33307325	ATGCTAATTCCGTTG[C/G]GATTGCTGGTGGACA	4799
rs367957234	snp	C/T	2.40474e-05	0.00346744	intron-variant	NFX1	GRCh38.p7	9:33364684	CAGGGACAGACAAAA[C/T]TAACTGGTGATTTCT	4799
rs368020538	snp	A/G	0.00517822	0.0506191	intron-variant	NFX1	GRCh38.p7	9:33323167	TCAGTTTGTACCCCT[A/G]AGGTTGTGCCATCCA	4799
rs368029011	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33344935	GGGAGGCTGAGATGG[A/G]CGGGTCACTTGAGGT	4799
rs368105486	snp	A/G	0.00398564	0.0444627	intron-variant	NFX1	GRCh38.p7	9:33290731	ATAGTGGCTCGGAAG[A/G]GCCAAGCCCCGCGCA	4799
rs368176377	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33359831	GAAGGTTATATAGAA[A/G]TTTATGGTAATATTC	4799
rs368179400	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33306833	TTATTCCCTCTCTCT[C/G]ATCCTTCCAGCAGCA	4799
rs368179981	snp	G/T	1.64789e-05	0.0028704	intron-variant	NFX1	GRCh38.p7	9:33303284	GTAAGTTTGTTTATA[G/T]ACACTGGAGTCTCTT	4799
rs368181444	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33329902	GACCTCAAGTGATCC[C/T]CCTGCCTCAGCCTCC	4799
rs368237285	snp	A/G	3.29625e-05	0.00405958	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33366711	ACTTGGCCCAAGTTT[A/G]TGGCCTGGAGAGCGT	4799
rs368251769	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33305105	TTGAGAACTTATTAA[C/T]GTTCAAGGCACTGTG	4799
rs368306537	snp	A/G			intron-variant, downstream-variant-500B	NFX1, LOC105376018	GRCh38.p7	9:33349104	CTAAAACATCAATGT[A/G]TTATCTTCGTACTGA	4799
rs368309277	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33314461	GCCGGTGGATCACTC[A/G]AGGTCAGCAGATTGA	4799
rs368313337	snp	C/T	0.00517822	0.0506191	upstream-variant-2KB	NFX1	GRCh38.p7	9:33289910	GGCCCCCAAGTGAGA[C/T]TGCACATTTAACTAC	4799
rs368384848	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33340070	GACAGTGGCCTTCTT[C/T]TCACAGCTCCACTAG	4799
rs368434544	snp	C/G			intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33366039	GATGGTTGCTTTAGC[C/G]CCTGTATCTAATGCT	4799
rs368437108	snp	A/C	1.65121e-05	0.00287329	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33313790	CAGATCATTTTGAAC[A/C]AGGGTAAGTGGTGGG	4799
rs368437934	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33332013	CTGTAGTTTTGTGAT[A/T]TTATCAGGTGTGCTC	4799
rs368490577	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33294275	ACCTTGAACCCATCA[A/C]CTTCACTGGAAACAT	4799
rs368598221	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33300790	AGACTTTGAGGGCAA[C/T]GGCTAGAGCCATCTC	4799
rs368598447	snp	G/T	0.0107246	0.0724382	intron-variant	NFX1	GRCh38.p7	9:33324224	TCTCTACTAAAAATA[G/T]AAAAATTAGCTGGGT	4799
rs368642720	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33295599	TCGCTGCTCCCTGCC[C/T]CAATAGGTAACCACT	4799
rs368658284	in-del	-/TC			intron-variant	NFX1	GRCh38.p7	9:33316817	TCATATTTCTGTCTC[-/TC]GTGCCTAGGAGAGCT	4799
rs368658880	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33344329	GCTGGTTCTCTGAAG[A/G]TGGGTCTGTGATCTG	4799
rs368694321	in-del	-/AAC	0.00523712	0.0509032	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352740	TGTTACTTAAATGTT[-/AAC]AACTGATGGCCTAGG	4799
rs368720615	snp	A/G			intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33349291	ATAGCAGTAATGCGG[A/G]AAATACAGAGGGCTA	4799
rs368743704	snp	C/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33306119	TTTTGTGATAGTCTG[C/G]AGATGAGGTTTTGGC	4799
rs368749977	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33308165	TATATCCATAAGCCA[C/G]ACACGGTGGCTCATG	4799
rs368773686	snp	C/T	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33314157	CCTTGCTAATTTTTG[C/T]GTTTTTAGTAGAGAT	4799
rs368831263	snp	A/G	3.46404e-05	0.00416161	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33354120	GCCTCTAAGATAACA[A/G]ACATGCAGCTTGGAG	4799
rs368867476	snp	C/G	0.000153988	0.00877328	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33294661	GACGTCTTTCCAGTC[C/G]TCTCCTTGTAATAAA	4799
rs368894456	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33357251	AGCTTGCAGTGAGCC[C/G]AGATGGTGCCACTGC	4799
rs368961737	snp	C/T	6.61037e-05	0.00574869	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33295009	GGAGGATGCTGGACC[C/T]GAAAGTACCAAACCT	4799
rs368993458	in-del	-/A			intron-variant	NFX1	GRCh38.p7	9:33326414	AAGCCTCTGTCTTTA[-/A]AAAAAAAAAAAAAAA	4799
rs369013664	snp	C/T	3.29522e-05	0.00405894	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33301332	AATTGGTTCGTGTCA[C/T]GGCCCCAGTGTGGAG	4799
rs369049349	snp	C/T	3.32016e-05	0.00407427	intron-variant	NFX1	GRCh38.p7	9:33311055	TGGGACAGCTTTGTT[C/T]GGGTTTGGATACATG	4799
rs369202003	snp	A/C	3.34521e-05	0.00408961	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33366770	GTGGTGGTCACTGCC[A/C]TCAGGTAGGTCAATC	4799
rs369206112	snp	C/G	1.65252e-05	0.00287443	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33290581	GCACGGGATGGCGGA[C/G]GCGCCTCCTGTCTCA	4799
rs369215940	snp	C/T	0.000214276	0.0103485	intron-variant	NFX1	GRCh38.p7	9:33303310	CTCTTTTACTACATA[C/T]ATTGTACCTCAGTTC	4799
rs369219626	snp	C/T	1.64814e-05	0.00287061	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33347073	GAGGAGAAGTGTCCC[C/T]CTTGCACTTTCCTAA	4799
rs369224470	snp	A/G	0.000153988	0.00877328	utr-variant-5-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33290524	GGCACGTGACCTGGT[A/G]ACAGTGCTGACTTGG	4799
rs369231841	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33336960	TACAAAAAATTAGCC[A/G]GCATGGTGGCAGGCA	4799
rs369310767	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33309507	CCTGCTCTTTTGTGG[C/T]TCTGGAGCTTTCACA	4799
rs369380208	snp	C/T	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33358121	GGTTTATTTTTCTTG[C/T]ATTACTTGTAATTTT	4799
rs369402940	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33360835	GTCTTTTGAAAAATT[A/G]GAAATCTAGCAGTGT	4799
rs369443633	snp	C/T	1.648e-05	0.0028705	intron-variant	NFX1	GRCh38.p7	9:33344229	TCAGCCTGCTCACAC[C/T]ATGTCATTTAGGATC	4799
rs369483942	snp	A/G	4.31118e-05	0.00464263	intron-variant	NFX1	GRCh38.p7	9:33342904	TTTTTTAGAAATTCA[A/G]ACATAATATACTTTG	4799
rs369493326	in-del	-/A			intron-variant	NFX1	GRCh38.p7	9:33345179	AAAAAGAAAAGAAAA[-/A]GAAAAAGAAAAAAAA	4799
rs369528056	in-del	-/A	0.0513736	0.151814	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33364824	AAGGCCAGCTTGATG[-/A]AAAAAAAAAAGCAAT	4799
rs369547635	snp	C/T	0.000437904	0.0147905	intron-variant	NFX1	GRCh38.p7	9:33332389	GATATTTGGGATATT[C/T]TTGTTACCTATGGCA	4799
rs369579784	in-del	-/A	0.0205511	0.0992634	intron-variant	NFX1	GRCh38.p7	9:33358509	CAGGTTGACATCCTC[-/A]AAAAAAAATGCAAAT	4799
rs369587898	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33341428	GGGAATTCAAGATAA[A/G]ATTTGGGTGGAGACA	4799
rs369595639	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33294329	TATACAAAGTTCTAA[A/G]GAAAGTAATTTTTAG	4799
rs369600703	snp	A/G	0.0193772	0.0965046	intron-variant	NFX1	GRCh38.p7	9:33319415	TTAGGAGCCTGTACT[A/G]TAATGAACACTATAT	4799
rs369624576	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33308730	CTATGCGGCTCGATA[C/T]AGAGTCTTTCTGGCA	4799
rs369679175	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33354014	TTTTAAAGAGGTCTT[C/T]TGTATCCCAAGTATA	4799
rs369721785	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33368396	TTAAAGAGAAAAGAA[A/T]ACCAAGTTGGCAAGG	4799
rs369747264	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33325300	TTAACAGTGGACTTC[A/T]CATCAGAAACAATGG	4799
rs369793511	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33345768	ATGGATGGGCCATAA[C/G]TTATTCAGTCAGTCT	4799
rs369808880	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33293208	CTTGGGCAAGTTCCT[A/G]CTCTCTGTGCTTCAG	4799
rs369822999	snp	C/T	4.94295e-05	0.00497115	missense, nc-transcript-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352683	GACGAAGAAAAGAGA[C/T]GGTGATTTGCTCTGA	4799
rs369846273	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33331276	GAATGGGCTTTTCCA[C/T]AGAAGTGAGTTTTCT	4799
rs369847725	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33361827	CATAGAGAGAAACGT[C/T]ATAGTGAAAAAAGGG	4799
rs369869945	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33341057	CACTTCCACATTTTC[A/G]GGTATCTTTTCAGCA	4799
rs369908425	snp	C/T	1.64746e-05	0.00287002	intron-variant	NFX1	GRCh38.p7	9:33318886	TTTATGCAACAATTA[C/T]GTAATAGTGTGTTTT	4799
rs369924690	snp	A/C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33362763	GGCTGTAGTGCAATG[A/C/G]CGCTATCTCAGCTCA	4799
rs369925284	in-del	-/TGAAG			intron-variant	NFX1	GRCh38.p7	9:33341569	ATTTATATATTTAAG[-/TGAAG]AGTGATGAATTGTGC	4799
rs369935401	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33297833	TTCTGTTTGATTTTC[A/T]ACTCTTTTAAAATGG	4799
rs369960617	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33346382	AGACATAGAGGGAAC[C/T]TCAGAGGAAGAGAAA	4799
rs369971699	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33326505	GGAAGGATCACTTGA[A/G]GCTAGGAGTTCAAGG	4799
rs370024512	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33356378	TATGAGTCCTTTGTT[A/G]GCTCTATGTATACAT	4799
rs370029072	snp	G/T	1.67253e-05	0.00289178	intron-variant, nc-transcript-variant	NFX1, LOC105376018	GRCh38.p7	9:33351545	TGAGAATCTGGCTAC[G/T]TCTGTCTCTCCTAGT	4799
rs370062801	in-del	-/A			intron-variant	NFX1	GRCh38.p7	9:33315724	AAACCAGTCTCTAAC[-/A]AACAACAAAAAAAAA	4799
rs370073603	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33321532	GCATGAAGAGCTCCC[A/G]TAGATCTGCTTCCCA	4799
rs370087497	in-del	-/GAGTTCTACT			intron-variant	NFX1	GRCh38.p7	9:33321495	ATAAGAGACTGGATA[-/GAGTTCTACT]TTAAAGATGGTAGCA	4799
rs370117392	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33290911	CTTCGACAGGCGGGC[A/G]TCGGCCAGGTCACAG	4799
rs370153125	snp	C/T			intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33353280	CATTTGTCATTGACA[C/T]AGCCAGGGCTAAGCT	4799
rs370192803	snp	A/C	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33359560	GCCGAGATGGCGCCA[A/C]CACACTCTAGCCTAG	4799
rs370193933	snp	A/C			intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352825	GTGGGAGTGGAGAAG[A/C]AACGAAGTCTGTAAC	4799
rs370209317	snp	A/G	1.64776e-05	0.00287028	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33295235	AACAACATGGGCCCC[A/G]TTCCAAAGGATGACC	4799
rs370210860	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33302849	TAATTTTTGCATTTT[C/T]AGTAGAGATGATGTT	4799
rs370217135	in-del	-/A			intron-variant	NFX1	GRCh38.p7	9:33358079	TCAGTAGATTTGTTT[-/A]CTTGCTTTTTGATGC	4799
rs370220750	snp	C/T	0.0115144	0.0749975	intron-variant	NFX1	GRCh38.p7	9:33335233	TTTCTTTTTCTTTTT[C/T]TTTTTTTTTTTTTTG	4799
rs370223065	snp	C/G	3.37678e-05	0.00410886	intron-variant, nc-transcript-variant	NFX1, LOC105376018	GRCh38.p7	9:33351537	CATGGAGATGAGAAT[C/G]TGGCTACTTCTGTCT	4799
rs370254207	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33346970	CCGTATGCCACTTAT[A/G]TGATGTATAATGGTT	4799
rs370264173	snp	A/G	0.00279162	0.0372561	intron-variant	NFX1	GRCh38.p7	9:33343607	AAAGGACTTGACTCG[A/G]TGTTTTTATTCTCTG	4799
rs370265170	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33319267	TATTTATGTAGGTAC[A/G]TTTTCTTTCCTCCTC	4799
rs370398830	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33291675	TTGGGAGGCCGAGGT[A/G]GACGGATCACGAGGT	4799
rs370453256	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33342236	GGAGGCCAAGGTGGG[C/T]GGATCATGAGGTCAG	4799
rs370460644	snp	C/T	0.0023933	0.0345097	intron-variant	NFX1	GRCh38.p7	9:33369141	CGCGATCTCAGCTCA[C/T]TGCAAGCTCCGCCTC	4799
rs370469107	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33326668	AGACTGCAGTCAGCT[A/G]TGATCATGCCACTGC	4799
rs370471178	snp	C/T	8.2426e-05	0.0064192	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33294616	TCAGCATAGTTATCA[C/T]CCGTCAGGAAGCAAA	4799
rs370561523	snp	A/G	1.64825e-05	0.00287071	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33294604	CTCTGCTGTTCATCA[A/G]CATAGTTATCATCCG	4799
rs370564230	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33327968	GGAGATTCAAGTCTA[C/T]ACTGGAGATGTGGGG	4799
rs370566457	in-del	-/GT			intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33366219	TCTGCTTGTGTGTCT[-/GT]ATCTGAATACTCACG	4799
rs370627870	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33315627	AGATTGGCCTGGGCA[C/T]GGTAGCTCATGCACT	4799
rs370641924	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33347652	AAAAGTAGATTTACC[A/G]TTTGATCCAGCAGTC	4799
rs370662577	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33329219	CAGGAAAGTATTACT[C/G]TCTCCGCTTCAGTGT	4799
rs370685754	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33315095	TTGGGGCGTGTTGGC[A/G]GGCGCCGGTAATCCC	4799
rs370780333	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33309213	ATATAAAAAATTAGC[C/T]GGGTGTGGTGGTGGG	4799
rs370786663	snp	A/T	0	0	intron-variant	NFX1	GRCh38.p7	9:33331776	GAGTACATGGCAACC[A/T]GTAAATGACATCAAA	4799
rs370789126	snp	A/G/T	9.97419e-05	0.00706137	intron-variant	NFX1	GRCh38.p7	9:33301469	TCCCCTATTTGATAC[A/G/T]TTTAAGTATTATTAA	4799
rs370802033	snp	C/T	3.52634e-05	0.00419886	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33364732	AAAGTTTGTCAGTGA[C/T]GTTGAGAAGGAAATG	4799
rs370839106	snp	G/T			intron-variant, downstream-variant-500B	NFX1, LOC105376018	GRCh38.p7	9:33349176	ACCTACTATGTGCTA[G/T]GTAACAGGCTAGGTT	4799
rs370855278	in-del	-/TA			intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33353424	TAGAGAATGAATGGT[-/TA]TATATATATATATAT	4799
rs370855733	snp	A/G/T	3.29654e-05	0.00405978	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33311149	TGCCCTGCCTTTATG[A/G/T]CAAAAACATGTGAAT	4799
rs370859788	snp	A/G	4.99205e-05	0.00499578	intron-variant	NFX1	GRCh38.p7	9:33290615	ATTGTCCCGGCCCGA[A/G]CGGGACTGGGCCCCT	4799
rs370866910	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33310743	CTTCTACAGGACCCT[A/G]TTAGCCATTCTGCCT	4799
rs370889022	snp	A/G	0.000153988	0.00877328	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33319030	AACTCCTCTCAGCCA[A/G]TTGCTAGAACTTGGA	4799
rs370968003	snp	A/C	0.000399281	0.0141238	intron-variant, downstream-variant-500B, nc-transcript-variant	NFX1, LOC105376018	GRCh38.p7	9:33348868	TTTGCTACATTCCAA[A/C]TGTCCTATACCAAAA	4799
rs370974863	snp	A/G	0.000248833	0.0111514	intron-variant	NFX1	GRCh38.p7	9:33328537	GGAGTATGAAAATGA[A/G]TAGTTGCAGTTTTCA	4799
rs371004081	snp	C/G			intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33349656	TGGTGAGGAAGCGTG[C/G]AAACAGGCCATTTTT	4799
rs371009472	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33338699	AAGTCACTGGGACAG[A/G]CCCCTAAGCAGCAGT	4799
rs371019732	snp	A/G	0.00279162	0.0372561	intron-variant	NFX1	GRCh38.p7	9:33362530	AAAGACAGACACCAC[A/G]CGATCTCACTCATAT	4799
rs371037122	snp	C/T	4.08739e-05	0.00452054	intron-variant	NFX1	GRCh38.p7	9:33354224	TGTGCCTTCTTTCTT[C/T]AATTAGACTTCAATT	4799
rs371080960	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33363085	AATAGCTAGAAAAGA[A/G]GCTTCTGTGTATTCT	4799
rs371092693	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33311733	AGTTTTTGTATTTTT[A/G]GTAGAGATGGGATTT	4799
rs371154935	snp	C/T	0.00636936	0.0560724	intron-variant	NFX1	GRCh38.p7	9:33319670	GCACACCACCACGCC[C/T]GGCTAATTTTTGTAT	4799
rs371208813	snp	A/T	8.24029e-05	0.00641831	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33295356	CTGTACGGAGGCAGG[A/T]TCCTCAAGTAGTATC	4799
rs371211163	snp	A/G	0.000413102	0.0143659	intron-variant	NFX1	GRCh38.p7	9:33366791	TAGGTCAATCCCGCC[A/G]TCAGAGGAAGAACTC	4799
rs371257333	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33332314	ATTCATATAGGGATT[A/G]GGCTCGCTCCAGACA	4799
rs371313077	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33364311	AGAACTGAACTTGGG[A/G]TAGGGTTGAGATAAG	4799
rs371316568	snp	A/C	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33324777	CTATATACAAAAAAA[A/C]AATTAGCCAGGTGTG	4799
rs371320881	snp	A/G	0.000278145	0.0117896	intron-variant	NFX1	GRCh38.p7	9:33332549	TGGGGTGAAAGTGTC[A/G]TCACTCTGAATCTTG	4799
rs371390697	in-del	-/A			intron-variant	NFX1	GRCh38.p7	9:33356991	GTGAAATGCTGTCTC[-/A]AAAAAAAAAAAAAAA	4799
rs371433824	snp	A/C/G	6.59308e-05	0.00574123	intron-variant	NFX1	GRCh38.p7	9:33311220	GACCTCAGTTTTCAC[A/C/G]TGCATGATTGACTTG	4799
rs371462577	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33323537	AGGCAGGAGGATCAC[A/G]AGGTCAGGAGTTCAA	4799
rs371626249	snp	A/G	6.64971e-05	0.00576577	missense, nc-transcript-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33351714	CCTGCACCACCCCCA[A/G]AGCTGACTGTGGTCA	4799
rs371631756	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33295980	CTGTTGCCCAGGCTA[C/G]AGTGCAGTGGTGCGA	4799
rs371659182	in-del	-/AAC			intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352825	TGGGAGTGGAGAAGA[-/AAC]AACGAAGTCTGTAAC	4799
rs371671936	snp	C/T	3.29881e-05	0.00406115	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352607	TTATTCACATAGTTC[C/T]AGTGTGCTAAAAGTC	4799
rs371690395	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33339845	TCAAATCTTAAAGCT[A/G]CAAAATGCTCTCCTT	4799
rs371720746	in-del	-/AT			intron-variant	NFX1	GRCh38.p7	9:33310993	AACAAATACAAAGAC[-/AT]GTCATAGTAGATGTA	4799
rs371736743	in-del	-/C			intron-variant	NFX1	GRCh38.p7	9:33345666	TAACTAGCTTTTTTT[-/C]CCCACTCTTATTATT	4799
rs371743619	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33360636	ACACACATATATACA[C/T]GCATACACCTGTGTG	4799
rs371782528	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33318145	TTTTTATAATACTGC[A/T]TTTATTCTGATCATT	4799
rs371796314	snp	A/C	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33361011	ATGGCTAGGGCACTA[A/C]GTGGCATTTCTGGAG	4799
rs371851347	snp	C/G	1.65737e-05	0.00287864	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294744	AGAAGCACCATATCA[C/G]AGTCAAGAAAGCACA	4799
rs371891898	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33293331	CTTATTATTAAACCT[A/G]AAACCCTCAGGCTCT	4799
rs371898611	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33329719	GATGGAGTGCAGAGG[C/T]GCAGTCTTGGCTCAC	4799
rs371946651	snp	A/G	0.000153988	0.00877328	intron-variant	NFX1	GRCh38.p7	9:33303290	TTGTTTATATACACT[A/G]GAGTCTCTTTTACTA	4799
rs371955568	snp	C/T	1.65121e-05	0.00287329	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33366736	GAGCGTGAGCTATGA[C/T]AGTGAACCGAAGCGC	4799
rs372055783	snp	C/G	1.64974e-05	0.00287201	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33301418	TCTCCAGCATCTCAA[C/G]CAGGTCAATTAATTC	4799
rs372075858	snp	A/T	0.00478085	0.0486577	intron-variant	NFX1	GRCh38.p7	9:33360002	GATGACTAGTAGTGC[A/T]GTCCAAATTTTCCTT	4799
rs372081059	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33355970	TTAAACTTGCTTGCT[C/T]TATATTTCTGTACAT	4799
rs372100668	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33316770	ATATTATTTAACCAG[C/T]TGTGACTCTACCTAA	4799
rs372106421	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33313288	GAAAAAGAAAAAGGA[A/G]GAGAAAGAAGAAAGA	4799
rs372167364	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33313985	GTCATTGTCCTATAT[A/C]ATTTTTTTTTTCTTT	4799
rs372188955	snp	C/G	0.000153988	0.00877328	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33366621	AGTCATCTTTTCCCT[C/G]AATACAGGGAAAGAA	4799
rs372216005	in-del	-/TTC			intron-variant	NFX1	GRCh38.p7	9:33323917	AGGCCCAAATGGAAA[-/TTC]TGAAGTTTAAAAGTA	4799
rs372221754	snp	A/G	0.00199481	0.0315187	intron-variant	NFX1	GRCh38.p7	9:33317464	GAAAAGAAATTGCAC[A/G]TGCACTTACTGGAAG	4799
rs372225324	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33337870	CCTGGCCAACATGGC[A/G]AAACCCTGTCTCTAC	4799
rs372241647	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33292306	TTAGCATCATCTTTA[A/G]CCCACACCCTCATCA	4799
rs372268103	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33333877	GGTCCAAGCCTGGTG[A/G]CTCATGCCTGTAATC	4799
rs372268858	snp	A/G	0.000153988	0.00877328	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33342754	TTCCCAGGATAAGGA[A/G]CACAAGTGTCCTTTG	4799
rs372282994	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33300842	CCTGCCCAGACTTGG[G/T]CTTCTTATAGCTGAC	4799
rs372294571	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33301963	TGTAATCCCAGCTAC[G/T]CGGGAGGCTGAGGCA	4799
rs372297665	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33340306	CATGGAAGCTGCCAA[A/G]GTTTGGTGCCTGCAC	4799
rs372329555	snp	C/T			intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33364914	AGGATCCTTATCTTT[C/T]TCAAAACACAGCCAT	4799
rs372376101	snp	A/T	3.50085e-05	0.00418366	utr-variant-3-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33369981	CGTCCAGGACTAAGA[A/T]GATCATGATGCACTT	4799
rs372428804	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33369508	AAATCACCAGCTCAT[A/G]TTTGTCCCACTATCA	4799
rs372435490	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33315724	AAAACCAGTCTCTAA[A/C]AACAACAAAAAAAAA	4799
rs372448867	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33298765	CTCTAGCCTGGGTGA[C/T]AGAATAAGAACCTGT	4799
rs372496855	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33327451	CTCACTGCAACCTCC[A/G]CCTCCCAGGTTCAAG	4799
rs372548732	snp	A/G	0.0123036	0.0774623	intron-variant	NFX1	GRCh38.p7	9:33335215	CTTCTTCTCTATTTT[A/G]TCTTTCTTTTTCTTT	4799
rs372591860	in-del	-/C			intron-variant	NFX1	GRCh38.p7	9:33336105	AATTTTTTTGAAAAA[-/C]CTGCCATTCTGTTTT	4799
rs372624000	snp	C/G	6.60928e-05	0.00574822	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33295025	GAAAGTACCAAACCT[C/G]TGGGGGTTTTCCACC	4799
rs372639564	in-del	-/C			intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33366189	CTAATTAAGAAACCC[-/C]AACAGATGTGTTTCT	4799
rs372663139	snp	A/G	1.64741e-05	0.00286998	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33303239	AGAATGTTTCTGCAC[A/G]TGTTCCTAATACCTA	4799
rs372707178	snp	C/G	0.00153489	0.0276603	intron-variant	NFX1	GRCh38.p7	9:33363967	ACTGCAAGATAGTTT[C/G]CCTCCCACTCCTTTT	4799
rs372793723	snp	C/T	0.000153988	0.00877328	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352714	AGCATCTAGTACTTA[C/T]CAAAGGTTAGTGTTA	4799
rs372813084	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33297911	TATAGGGTATGCATA[A/C]CAGGGAGGTGGGAAT	4799
rs372838405	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33347239	AGAAGCTTTCCATTG[C/T]TTAAAAATTTTTTCT	4799
rs372917152	snp	A/G	0.000131852	0.00811842	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33307276	GAAACAGCCTGGCCA[A/G]GACTGCCCACATTCC	4799
rs372928232	snp	C/G/T	6.62142e-05	0.0057535	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33366749	GACAGTGAACCGAAG[C/G/T]GCAATGTGGTGGTCA	4799
rs372944918	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33304003	CGGGCTTAGTGGCTC[A/G]CGCCTGTAATCCCAG	4799
rs373011882	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33291127	CCGCCCTGTACTGTA[A/C]CTATTCTGTAATTGT	4799
rs373028874	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33346981	TTATATGATGTATAA[C/T]GGTTTACATGGCTTT	4799
rs373071101	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33336744	TAGCTGGGACCACAG[A/G]CATGTGCCACCATGC	4799
rs373099050	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33314716	ATGTGAAATCTAAGA[A/T]CATATAAAACTAATT	4799
rs373110354	snp	A/G/T	4.95662e-05	0.00497806	intron-variant	NFX1	GRCh38.p7	9:33347014	TTAGAAAGTATTCCT[A/G/T]AAGTTACCTTTCTCT	4799
rs373144085	snp	G/T	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33331307	AGATAAATAAAACAT[G/T]TCTTAAAACTTCAAA	4799
rs373220020	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33315318	AATATTGTCAGTTAC[A/C]CAGTCGCTGATTAAA	4799
rs373222370	snp	A/G	1.64787e-05	0.00287038	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33318978	GCCAGCAATGCCCAC[A/G]GCTCCCCCAGCTGGT	4799
rs373228798	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33302240	CTCAAATATTTATCA[C/T]TTCTTTGTGTTAGGA	4799
rs373292864	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33366787	CAGGTAGGTCAATCC[C/T]GCCGTCAGAGGAAGA	4799
rs373353689	snp	C/G/T	3.30777e-05	0.00406669	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33290590	GGCGGAGGCGCCTCC[C/G/T]GTCTCAGGTATTGTC	4799
rs373380372	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33308515	AAATGCACAGTAATA[A/G]AAAAACAGTTGATCA	4799
rs373420105	snp	G/T	4.54349e-05	0.00476607	intron-variant	NFX1	GRCh38.p7	9:33342861	GGCAAGCCAGTGAGT[G/T]TCTTTACTGTATAGT	4799
rs373421855	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33342408	CGGAACTTGCAGTGA[A/G]CCAAGATTGCTCCAC	4799
rs373438521	snp	C/T	1.73117e-05	0.00294203	intron-variant, splice-donor-variant	NFX1, LOC105376018	GRCh38.p7	9:33351510	GAAAGTTAAAACTCA[C/T]CCCAAATCCCACATG	4799
rs373449739	snp	A/C	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33346536	ATAGGAACTGAGACA[A/C]CAGGAAGTGTGAGGG	4799
rs373451616	snp	C/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33303569	TGGACGTGGGCTTCA[C/T]CTCACCCCCAGCAGT	4799
rs373496384	snp	A/G			intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33350865	TATTTTAAAAACTGA[A/G]CTGAGTGTGGTGGTT	4799
rs373551125	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33346817	CTTCTGTTTTGGCAT[A/G]TCTCTTCCTCCTTGG	4799
rs373680264	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33339441	AAAGACCTGCCCCCA[C/T]GATTCAATTACCTCC	4799
rs373698155	snp	A/C			intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33353448	TATATATCTGGTTAG[A/C]TGGGGAGAGGTGCCA	4799
rs373705471	snp	C/G			upstream-variant-2KB	NFX1	GRCh38.p7	9:33289287	GACTTAGTTGGGGCG[C/G]GGGGCCCAGCTCCTG	4799
rs373755493	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33343391	AAAAAGTAGAATAGC[A/G]GATACTTGGTTTAAT	4799
rs373781580	in-del	-/GAAA			intron-variant	NFX1	GRCh38.p7	9:33304292	TAAAATAAAAACAAA[-/GAAA]TCACCAATGACTCCT	4799
rs373783350	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33331935	AGACCTTTTAGACCA[C/T]TCACATGTAGTGGAA	4799
rs373826450	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33320997	GCATTAGGAAAGCCA[A/G]TCATCTGTTGGTTCT	4799
rs373836457	snp	A/C/G	4.96844e-05	0.00498399	intron-variant	NFX1	GRCh38.p7	9:33311097	TTCAGTGAAACCTTT[A/C/G]TCTTTCAGTCTCTGC	4799
rs373861419	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33360080	TGCCCTTTAGGAACC[C/G]TCAGTCAGTGTTCTC	4799
rs373882246	snp	A/G	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33330315	CAGCATCTGACTTGC[A/G]AATAATTCTGAGGAT	4799
rs373993909	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33343882	ATCTGTTCATGCCTT[C/T]TTCACCAGCTTAGCT	4799
rs374004773	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33299401	CTTATTCAGGGAAGA[C/T]TTTTGTTTAATTTGG	4799
rs374025948	snp	A/G	1.67601e-05	0.00289478	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33354889	CAGCCTTGGAAAGGA[A/G]AAAGTAAGTAGTTGC	4799
rs374033783	snp	C/G/T	4.95457e-05	0.00497703	intron-variant	NFX1	GRCh38.p7	9:33313631	TTACACTGATGCTGT[C/G/T]TTTACATCTATTGTC	4799
rs374064978	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33355723	GATCTTGGCTCACTG[C/T]CACCTCTGCCTCCCG	4799
rs374114239	snp	G/T	1.67349e-05	0.0028926	intron-variant	NFX1	GRCh38.p7	9:33290639	GGCCCCTTTCAGGGA[G/T]CGGAAATTGGGTCAG	4799
rs374181403	snp	G/T	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33359193	ATTTTTTTCCTTTCT[G/T]TTTTCTTTTATCTTT	4799
rs374324777	in-del	-/T			intron-variant	NFX1	GRCh38.p7	9:33357705	CTGGCTAAGATTTTC[-/T]TTTTTTTTTTTTTTT	4799
rs374420266	snp	A/G			missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33313689	AGGCTGTCTCAGTCC[A/G]CTGTTCTAACCCATG	4799
rs374429183	snp	A/G	8.24368e-05	0.00641963	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33294619	GCATAGTTATCATCC[A/G]TCAGGAAGCAAACCT	4799
rs374434585	snp	C/T	6.59044e-05	0.00574002	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33295272	AAAGACCAGCAAAAT[C/T]TACCTGTGACAGTGA	4799
rs374444090	snp	C/T	0.000232223	0.010773	intron-variant, nc-transcript-variant	NFX1, LOC105376018	GRCh38.p7	9:33351555	GCTACTTCTGTCTCT[C/T]CTAGTTTCGGAGCAA	4799
rs374449355	snp	A/G	0.00517822	0.0506191	intron-variant	NFX1	GRCh38.p7	9:33316996	AGCCTACTAGCAAAA[A/G]CTTCCAGTTTCCAGG	4799
rs374510461	in-del	-/A			intron-variant	NFX1	GRCh38.p7	9:33330875	AAAGTAAAAAAAAAA[-/A]CTCTTCAAAAAGCTG	4799
rs374548304	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33339001	AAAAATTATTAGGAC[A/T]TTTTTTAAAAAGATT	4799
rs374572877	snp	C/T	0.000132044	0.00812431	intron-variant	NFX1	GRCh38.p7	9:33328567	ATTTCCAGCTCTTTT[C/T]GTTTTTATTAAAGAT	4799
rs374577223	snp	C/T	3.29516e-05	0.00405891	intron-variant	NFX1	GRCh38.p7	9:33318907	AGTGTGTTTTCTTAA[C/T]AGGGACTTGAAATGC	4799
rs374581221	snp	C/T	1.71499e-05	0.00292825	intron-variant	NFX1	GRCh38.p7	9:33338608	AGTGGACTTATTAGG[C/T]ATAATCAGATTCCAT	4799
rs374600511	snp	A/G	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33305832	GTGAGCAGAACATAC[A/G]GTGAAATATGTCCAA	4799
rs374601839	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33367961	ACTCTGGGCCGGGCG[C/T]GGTGGCTCACGCCTG	4799
rs374686901	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33327190	ATATTTTTGAGTTTT[G/T]ATTTATTTATTTTTT	4799
rs374709626	snp	A/C	0.0240643	0.107019	intron-variant	NFX1	GRCh38.p7	9:33306348	CTTTGACTGTGGATA[A/C]AGCCAGTTTGAGGTG	4799
rs374711006	snp	A/G	0.00011602	0.00761554	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33366753	GTGAACCGAAGCGCA[A/G]TGTGGTGGTCACTGC	4799
rs374745429	snp	A/G			downstream-variant-500B	NFX1	GRCh38.p7	9:33371353	GGACCCATGTAGTGC[A/G]GGTCAGTGGCCCCAC	4799
rs374753518	snp	A/G	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33322378	AGATCTCCACTCAGG[A/G]TAAGTGTGGACAAGA	4799
rs374772335	snp	C/G	1.96485e-05	0.0031343	intron-variant	NFX1	GRCh38.p7	9:33369856	TCTGAAGTCCTGTAT[C/G]TGTTTCCCCCAAAGA	4799
rs374775205	in-del	-/T	0.00358779	0.0422022	intron-variant	NFX1	GRCh38.p7	9:33305508	GATGTTGGGACTTCA[-/T]TTGGAAGGCTGTGGG	4799
rs374892295	snp	C/G/T	3.29995e-05	0.00406185	utr-variant-5-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33290554	GCTGTACAGCTCGAT[C/G/T]TAGGTTCTGCGGCAC	4799
rs374900080	snp	C/T	0.000131861	0.00811869	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294605	TCTGCTGTTCATCAG[C/T]ATAGTTATCATCCGT	4799
rs374936089	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33341337	TGAGACTTATTCACT[A/G]TCATGAGAACAGCAC	4799
rs374996886	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33312765	AGCCCCAGCTACTGG[C/G]GAGGTTGAGGTAGGA	4799
rs375050155	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33310914	TCTGTGGTGATAATG[A/T]TGTCGATTTTTTGCA	4799
rs375084412	snp	G/T	3.40866e-05	0.00412822	intron-variant	NFX1	GRCh38.p7	9:33364129	TAACTTGTTACCTGC[G/T]TTCTTAATTGTGGCT	4799
rs375115358	snp	A/G	0.000230745	0.0107387	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33313762	GTGCCATGGGGGTCA[A/G]TGCCAGCCTTGCCAG	4799
rs375121826	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33353738	CTGTTGCCCAGGCTA[C/G]AGTGCAATGGTGCAA	4799
rs375220771	snp	A/G	1.66701e-05	0.002887	intron-variant	NFX1	GRCh38.p7	9:33328713	AGAGTTGTTGCCATC[A/G]ATGTTTTCTTTAAAA	4799
rs375249619	snp	A/C	0.000329592	0.0128331	intron-variant	NFX1	GRCh38.p7	9:33303307	AGTCTCTTTTACTAC[A/C]TACATTGTACCTCAG	4799
rs375261165	snp	C/T	8.26726e-05	0.0064288	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33366744	GCTATGACAGTGAAC[C/T]GAAGCGCAATGTGGT	4799
rs375319253	snp	A/G	4.95193e-05	0.00497566	intron-variant	NFX1	GRCh38.p7	9:33301426	ATCTCAAGCAGGTCA[A/G]TTAATTCTCTCTTCT	4799
rs375328223	snp	A/G	1.98253e-05	0.00314838	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33351809	GGTATTTCTGGCCAC[A/G]GATGCAGCATTGACT	4799
rs375333719	snp	C/T	0.000153988	0.00877328	intron-variant	NFX1	GRCh38.p7	9:33318842	GCAAGTAAGGTTTTA[C/T]GTTTTCTTCAGTTGA	4799
rs375351181	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33339898	GTAACACTGATGCAG[A/G]AAGTGGGTTCCCATG	4799
rs375355160	snp	A/G	3.29821e-05	0.00406078	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352609	ATTCACATAGTTCCA[A/G]TGTGCTAAAAGTCGT	4799
rs375359318	in-del	-/C			intron-variant	NFX1	GRCh38.p7	9:33355641	AAACTGTTAAGAATT[-/C]TTTTTTTTTTTTTTT	4799
rs375373383	snp	A/C			intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33366622	GTCATCTTTTCCCTC[A/C]ATACAGGGAAAGAAT	4799
rs375602205	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33300449	TTATTCTTTTAACTT[A/G]TTTAGACCTGAAAGC	4799
rs375608804	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33300541	ACACACACTCACACT[C/G]AGTTTTGAGAGTATC	4799
rs375626132	snp	A/G	0.000153988	0.00877328	intron-variant, nc-transcript-variant	NFX1, LOC105376018	GRCh38.p7	9:33351532	TCCCACATGGAGATG[A/G]GAATCTGGCTACTTC	4799
rs375644351	snp	A/G			upstream-variant-2KB	NFX1	GRCh38.p7	9:33290024	AAAAAAAAAAAAAAA[A/G]TCTGGAGCCAGGCGT	4799
rs375675666	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33328073	TGGAGTTCAGTGGTG[C/T]GATCACAGTTCACTG	4799
rs375687870	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33358781	GATCCTCCCACCTCA[C/T]CTCCCAAGTAGCTGG	4799
rs375688180	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33292635	GTTTCCCTTCCTCAT[A/G]TCTCTTATGGGTTTT	4799
rs375688478	snp	C/T	0.00517822	0.0506191	intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33351245	GGTGGATCGCTTCCA[C/T]TCAAGAGTTCGAGAC	4799
rs375693406	snp	A/T			intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33349594	TTTCGAGGGTTCAAG[A/T]CTAGCCTTTGGTCCT	4799
rs375742474	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33324890	GCTGAGATTGTGCCA[C/T]TGCACTCCAGCCTGG	4799
rs375818086	snp	A/G	0.000148801	0.00862429	intron-variant	NFX1	GRCh38.p7	9:33307321	TGGAATGCTAATTCC[A/G]TTGGGATTGCTGGTG	4799
rs375821284	snp	C/T			utr-variant-3-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33370899	TGGACTCTGTTTGAA[C/T]ATTCCAAGTAGTATA	4799
rs375843228	snp	A/G			intron-variant, utr-variant-3-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33347912	ACCATTATTCTAAGT[A/G]AAGTAACTCAGGAAT	4799
rs375851013	snp	A/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33296424	CTGACGAAGTCTTAC[A/T]CATTTTTCAAAAGCT	4799
rs375851097	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33347616	CCACTGTGGAAAACT[A/G]TGGAGATTCCTTAAA	4799
rs375857091	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33305077	AGGGGACCATTAATT[G/T]AACATGTTTTTATTG	4799
rs375872260	snp	A/G	0.000437904	0.0147905	intron-variant	NFX1	GRCh38.p7	9:33332559	GTGTCGTCACTCTGA[A/G]TCTTGTTAGGGAGTT	4799
rs375917548	snp	A/G	3.29571e-05	0.00405924	intron-variant	NFX1	GRCh38.p7	9:33303281	GTGGTAAGTTTGTTT[A/G]TATACACTGGAGTCT	4799
rs375957446	snp	A/G			intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33351321	AAAAATTAGCTGGGC[A/G]TGGTGGCATGCACCT	4799
rs375984192	snp	A/C/G	0.000275972	0.0117437	intron-variant	NFX1	GRCh38.p7	9:33354052	TCTTGTGAAACTGCA[A/C/G]TGCCTCTTTTTCCCT	4799
rs375996194	in-del	-/AGACTGGA			intron-variant	NFX1	GRCh38.p7	9:33321485	CAGCTTCAGTATAAG[-/AGACTGGA]TAGAGTTCTACTTTA	4799
rs376066384	snp	A/G	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33328898	GTAGCACTGTTGCAA[A/G]GAGTCAGCCAACTAA	4799
rs376137574	snp	A/G	0.00914312	0.0669923	intron-variant	NFX1	GRCh38.p7	9:33343452	TGCATCCAGTCTGTC[A/G]TGATATAGTTGAGGC	4799
rs376184617	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33325396	TGGCCGGGCGCGGTG[A/G]CTCACGCCTGTAATC	4799
rs376262177	snp	C/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33309427	ATGACTACCAGAGAT[C/T]AAAACTGTTGCAGAT	4799
rs376342253	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33336370	ACAGGTGCCCGCCAC[C/T]GCGCCCGGCTAATTT	4799
rs376344091	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33361418	TAGCATATGCATTAC[C/T]TCACATTCTTATTTT	4799
rs376352872	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33369157	TGCAAGCTCCGCCTC[C/G]CGGGTTCATGCCATT	4799
rs376449133	snp	A/G	4.94393e-05	0.00497164	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33295343	CAAGAGAAATGCACT[A/G]TACGGAGGCAGGATC	4799
rs376458805	snp	A/C	0.000153988	0.00877328	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33351709	GCAGCCCTGCACCAC[A/C]CCCAGAGCTGACTGT	4799
rs376496607	snp	C/G	1.65239e-05	0.00287431	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33294958	AGTCAAGGGGAAACT[C/G]AAATGTGAATGGAGT	4799
rs376499865	snp	G/T	0.00199481	0.0315187	intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33350045	GTGGTTTCTCATGCC[G/T]GTAATCCCAACACTT	4799
rs376521545	snp	A/G	0.000118945	0.00771092	intron-variant	NFX1	GRCh38.p7	9:33342882	ACTGTATAGTTTATT[A/G]GAAGAGTTTTTTAGA	4799
rs376551960	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33337383	AAATATTATACCATT[C/T]TGTATAAGAGACTTC	4799
rs376566477	in-del	AA/G			intron-variant	NFX1	GRCh38.p7	9:33309369	CTCAGAGAAAAAAAA[AA/G]AAAACTTAATCCTCT	4799
rs376586763	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33347651	TAAAAGTAGATTTAC[C/T]GTTTGATCCAGCAGT	4799
rs376601260	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33361195	ATTAAAATATGGGAA[C/T]ATAATTAGAAGACTA	4799
rs376633595	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33367437	TAGTGCCAAAATCAA[A/G]GGCTGAGTTTCTAGC	4799
rs376637523	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33344699	GGTGAAACCCCGTCT[C/T]TACTAAAAATACAAA	4799
rs376669810	snp	A/G	3.34728e-05	0.00409088	intron-variant	NFX1	GRCh38.p7	9:33354900	AGGAAAAAGTAAGTA[A/G]TTGCAGCTGCTTTTT	4799
rs376731860	snp	A/G			upstream-variant-2KB	NFX1	GRCh38.p7	9:33289495	GTCTGGGGGGTGGGG[A/G]GGTGGGGAGAAGCGT	4799
rs376743181	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33295560	TCAATCTTTATTCAC[C/T]GTCTGCCTAAGTTCT	4799
rs376762913	snp	C/T	0.0209421	0.100162	intron-variant	NFX1	GRCh38.p7	9:33330569	TCATAAATTTAGTAA[C/T]GCCCAGAGATGCTCT	4799
rs376774733	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33362805	GCCTCCCGGGTTCAA[A/G]CGATTCTCCTGCCCC	4799
rs376952589	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33323066	TCCTTGAGACTGAGC[A/G]TAATCCAAATAAGGC	4799
rs376962209	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33362952	CAGGTGATCCGCCCG[C/T]CTCGGCCTCCCAAAG	4799
rs376981641	in-del	-/G			intron-variant	NFX1	GRCh38.p7	9:33326126	AAATTTTGTATAAGA[-/G]GGGGGGCTAGGCGCA	4799
rs377024514	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33299029	TAGTAGAGAAAAAGG[G/T]GTTTGTCTGTAAAAT	4799
rs377168957	snp	C/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33357170	AGCCGGGCATGGTGG[C/T]GGGCACTTGTAGTCC	4799
rs377170977	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33314265	GCTGGGATTACAGGC[A/G]TGAGCCACAGTGCCT	4799
rs377172307	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33364123	GGTATGTAACTTGTT[A/G]CCTGCTTTCTTAATT	4799
rs377214937	in-del	-/G	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33327087	TAGAATAACAAAAAA[-/G]ACATGAGACTTACAG	4799
rs377241987	snp	A/G	1.64727e-05	0.00286986	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33344154	CCCTGAATGTACCCA[A/G]ACCTGCGCTAGAGTC	4799
rs377263790	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33340414	CCGAGGCTGCATGCA[A/G]CAGGGGGACCCTGGG	4799
rs377267697	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33360415	ACTCATAAAGCTCTT[A/G]GCACAAGAGCTTGGC	4799
rs377273725	in-del	-/AT			intron-variant, utr-variant-3-prime	NFX1	GRCh38.p7	9:33347946	AACCAAACATCGTAT[-/AT]GTTCTCAATTATAAG	4799
rs377275937	snp	A/C/T	8.24349e-05	0.00641965	synonymous-codon, stop-gained, nc-transcript-variant	NFX1	GRCh38.p7	9:33295160	GAGGGGGCCAGGCCA[A/C/T]GACCAGGCAGAAATC	4799
rs377306755	in-del	-/ATT	0.00676609	0.0577691	intron-variant	NFX1	GRCh38.p7	9:33358443	TTTAATTTTTTTTAA[-/ATT]ATTATTATTATTTAA	4799
rs377323484	snp	C/T	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33315440	TGCTTCCCTGAAATA[C/T]ACTCTCTCCTTCGTC	4799
rs377357077	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33342080	AAGATCGCACCACCA[C/T]ACTCCAGCCTGGGCA	4799
rs377363424	snp	A/G			intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352824	AGTGGGAGTGGAGAA[A/G]AAACGAAGTCTGTAA	4799
rs377389070	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33308764	GATCAAAAAATGACA[A/G]TTCTTACTTTTACTA	4799
rs377392856	snp	C/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33331518	AGTGTTCACTGATGG[C/G]AGCATTAACTCAGTT	4799
rs377410038	snp	C/G	1.65072e-05	0.00287286	intron-variant	NFX1	GRCh38.p7	9:33347022	TATTCCTAAAGTTAC[C/G]TTTCTCTTTCTGCAG	4799
rs377421189	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33346910	TTACTTTCCTGTGAC[C/T]GTTTTTCAAAAGTAC	4799
rs377619617	snp	A/G	0.0001318	0.00811681	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33318923	AGGGACTTGAAATGC[A/G]GTAACCATACATGTT	4799
rs377668136	snp	A/G	1.64738e-05	0.00286995	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33367577	GGGAAATGCAGGCAC[A/G]GCCTCCACCACCGAT	4799
rs377672232	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33353138	CCTAACTTTAGTGTG[C/T]AAAATAACTTTGAAA	4799
rs377682621	snp	A/G	4.94442e-05	0.00497188	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294539	GGTAGAAGAAATTAC[A/G]GTTCACCACCTCCCT	4799
rs377685245	snp	C/T	3.3066e-05	0.00406595	intron-variant	NFX1	GRCh38.p7	9:33313621	ACAGGAACTTTTACA[C/T]TGATGCTGTCTTTAC	4799
rs386414854	in-del	-/AAA			intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352826	GGGAGTGGAGAAGAA[-/AAA]ACGAAGTCTGTAACT	4799
rs386734347	multinucleotide-polymorphism	CTCA/TGAT			intron-variant	NFX1	GRCh38.p7	9:33298880	TGTTCAGGTAGGAGA[CTCA/TGAT]GGAGACTTAGACTGG	4799
rs386734348	multinucleotide-polymorphism	CAT/TAC			intron-variant	NFX1	GRCh38.p7	9:33301851	CCAAGGCAGGCGGAT[CAT/TAC]CTGAAGTCAGAAGTT	4799
rs386734349	in-del	AGACTGGATAGAGTTCTACT/TA			intron-variant	NFX1	GRCh38.p7	9:33321485	CAGCTTCAGTATAAG[AGACTGGATAGAGTTCTACT/TA]TTAAAGATGGTAGCA	4799
rs386734350	in-del	ATA/TGTT			intron-variant	NFX1	GRCh38.p7	9:33342979	TTCGTATTTCCAATA[ATA/TGTT]GAGACTTTTTTTAAA	4799
rs397703268	in-del	-/TT			intron-variant	NFX1	GRCh38.p7	9:33331709	TTTTTTTTTTTTTTT[-/TT]CAGGATAATTTTTAC	4799
rs397765712	in-del	-/A	0	0	intron-variant	NFX1	GRCh38.p7	9:33318001	AAAAAAAAAAAAAAA[-/A]TCTTCATTATAGTGA	4799
rs397774432	in-del	-/A	0.375	0.216506	intron-variant	NFX1	GRCh38.p7	9:33329657	TAAATAAATAAAATT[-/A]AAAAAAAAAAAAGAA	4799
rs397812977	in-del	-/A	0	0	intron-variant	NFX1	GRCh38.p7	9:33309374	AGAAAAAAAAAAAAA[-/A]CTTAATCCTCTGCAT	4799
rs397893907	in-del	-/T			intron-variant	NFX1	GRCh38.p7	9:33311570	GATTTTTTTTTTTTT[-/T]GAGACGGAGTCTCGG	4799
rs397894834	in-del	-/A			intron-variant, utr-variant-3-prime, downstream-variant-500B	NFX1, LOC105376018	GRCh38.p7	9:33348517	AAAGAAAAAAAAAAA[-/A]TCACTGATTGCAGGT	4799
rs398046534	in-del	-/CC	0.5	0	intron-variant	NFX1	GRCh38.p7	9:33342210	CATGCCTGTAACCCC[-/CC]AGCACTTTGGGAGGC	4799
rs527265436	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33331175	TCTCAAAAAAAAAAT[A/T]AAAAAAATAAGCTGA	4799
rs527309826	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33306258	TTTTGAGCGTGTGTG[A/G]CTCTGACAGAGTTGA	4799
rs527345370	snp	C/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33363738	CCATTCTCAGTGATC[C/G]CACACCCCCAAACTC	4799
rs527382731	snp	G/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33313289	AAAAAGAAAAAGGAG[G/T]AGAAAGAAGAAAGAG	4799
rs527385713	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33322496	CAACTCCAAGTTGAA[A/G]AGGCTGAAATTCTGG	4799
rs527410269	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33291888	AGCCTGGGCGACAGA[A/G]TGTGACTTCGTCTCA	4799
rs527488256	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33296076	GGATTACAGGCGCCC[A/G]CCACCATGCTTGGCT	4799
rs527556074	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33324364	AGCCTGGACGAGGGA[A/G]TAAGACTCCATCTCA	4799
rs527616130	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33343451	CTGCATCCAGTCTGT[C/T]GTGATATAGTTGAGG	4799
rs527736143	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33296810	TCTTACAGCCCTCAC[A/G]CTTATGTCTTTCTCT	4799
rs527770813	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33341624	AGAAGGCTTAAAGAC[G/T]TCCTCTTATTATAAA	4799
rs527823905	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33298683	CAGCTACTCAAGAGG[G/T]TGAACTAGGAGGATC	4799
rs527865724	snp	C/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33369158	GCAAGCTCCGCCTCC[C/T]GGGTTCATGCCATTC	4799
rs527871046	snp	A/G	0.0023933	0.0345097	intron-variant	NFX1	GRCh38.p7	9:33317141	AATTGCATATAGGCC[A/G]GGTGTAGTGGCTCAC	4799
rs527902838	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33362982	GTGCTGGGATTACAG[A/G]CGTGAGCCACCGTAC	4799
rs527923622	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33321606	CAAGGCTGGGCATGG[C/T]GGCTCATACCTATAA	4799
rs527959387	in-del	-/A			intron-variant	NFX1	GRCh38.p7	9:33355624	TAGACTATTACAAAT[-/A]AAAACTGTTAAGAAT	4799
rs527967022	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33309275	TGCAGGAGAATGGCG[G/T]GAACCCGGGAGGCGG	4799
rs527995601	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33335565	TTAAAAATATGTTGA[A/G]ACAGGGTCTCACTTT	4799
rs528002430	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33328307	TGGAATTATAGGCAT[G/T]AGCCACCACACTTGG	4799
rs528027228	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33332677	ATTCTAATTGATGAA[A/C]TGCTGAAAAATATAA	4799
rs528089274	snp	C/T	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33294202	ACACTTAGCTGTCAT[C/T]GGCTATTGGTGTTTG	4799
rs528140592	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33293482	CAACTCTTTGATATA[A/G]AGGTTGTTACTATCT	4799
rs528161985	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33338118	TCAGCACTTTGGGAG[A/G]CCATGGGAGGTGGAT	4799
rs528215450	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33345632	TAAAAGTGGGATCCT[A/G]CTGAACTTAATGCTT	4799
rs528264384	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33340913	ACATTATTGTCCATA[A/T]CATTATCAGCATTTT	4799
rs528274006	snp	C/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33298513	CTGGATGTGGTGGCT[C/T]ACATCTGTAATCCCA	4799
rs528308150	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33326241	AACATGGTGAAACTC[C/T]GTTTCTACTAAAAAT	4799
rs528328741	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33318206	TTTCTTTTTGGCAAC[A/G]GGGACCTTTTTACAA	4799
rs528365710	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33325678	CAAAAAAAGAAAAAG[A/G]AAAAAAGAAAACTGT	4799
rs528383523	snp	C/T	0.00279162	0.0372561	intron-variant	NFX1	GRCh38.p7	9:33332908	CAGAGTGCAGTGGCG[C/T]GATCTCGGCTCACTG	4799
rs528485249	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33364479	GCTCTTATTTTTCTC[C/G]TGGAGTCCCTGGCCT	4799
rs528554307	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33323565	CAAGACCAGCCTGGC[C/T]GACATGGTGAAACCC	4799
rs528571954	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33331041	CACGGTGGTGGGCGC[C/T]TGTAGTCCCAGCTAC	4799
rs528610767	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33337168	AACACACTCAGCCAG[C/T]CTTCCATATCCATGG	4799
rs528686732	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33308640	TTAATTTATCTAAGC[C/T]TGCATCTGTAAAATA	4799
rs528720056	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352494	CAACTGTGTCAGTTT[A/G]CATGTGTGGTTAGCT	4799
rs528727631	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33307890	CTCACTGCAACCGCC[A/G]CCTCTTGTGCTCAAG	4799
rs528739542	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33365884	AGACTCCTTCAGAAG[A/G]GGGAGACCCCTGTCC	4799
rs528782071	snp	A/G	1.65378e-05	0.00287552	missense, nc-transcript-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33351693	TGGATGAGCCCTGCA[A/G]GCAGCCCTGCACCAC	4799
rs528881492	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33293407	GTAGTCCTAACAGCA[A/G]TGATAGAGTACCATT	4799
rs528920471	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33292748	TAGTTGCATCAACTC[A/G]TTACTGCTTAACGAG	4799
rs528948319	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33344904	CAGTGGCTCATGCCT[A/G]TAATCCTAGCACTTT	4799
rs529061290	in-del	-/TATT	0.00398564	0.0444627	intron-variant	NFX1	GRCh38.p7	9:33361341	AATAAAAATGGTATA[-/TATT]TATGGTAATACAGCA	4799
rs529078110	snp	C/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33366234	GTATCTGAATACTCA[C/G]GATTTTTAAAGTAGA	4799
rs529169544	snp	A/G	0.00318978	0.0398085	intron-variant	NFX1	GRCh38.p7	9:33338009	AGCCAAGATTGCGCC[A/G]TTGCACTCCAGCCTG	4799
rs529190795	snp	A/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33331385	TGTGTCTATGTCTTC[A/T]TAAAGCATGCTATAT	4799
rs529286269	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33370127	AAAGCATGAGTGTGT[C/G]AGAAATCCCTTGTCT	4799
rs529295106	snp	A/G	0.0023933	0.0345097	intron-variant	NFX1	GRCh38.p7	9:33322700	TCCCACCCAGCACCC[A/G]GAGTAGTGCCTCAGA	4799
rs529325314	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33370581	ATTTTGGCATTTTCA[A/G]TGTGATCAGTTCTAG	4799
rs529352865	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33329820	CATGCCATCACACCC[A/G]GCTAATTTTTGTATT	4799
rs529385908	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33336405	ATTTTTAGTAGAGAT[A/G]GGGTTTTACCATGTT	4799
rs529438655	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33318518	CTTTTTTAATTTCTT[A/C]CTATGGTAAAGCTCT	4799
rs529460989	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33357857	GCCCATTTCCACTTA[C/T]ATTTCACAATTGGCT	4799
rs529481707	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33316176	AATGGGATAATATGT[C/T]CCAGCCCCTGTTTTT	4799
rs529487425	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33307667	CATATGTTTTATCCC[A/G]CATTGATATCCAGGT	4799
rs529498453	snp	A/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33306884	GTCCAGTTATAGACG[A/T]CTTGTCTTATAGGTA	4799
rs529517444	snp	A/G	0.00199481	0.0315187	intron-variant	NFX1	GRCh38.p7	9:33315507	TCAAAATCAGCTGTC[A/G]TATATTCTTTCCCCA	4799
rs529552662	snp	C/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33323497	TGGTGGCTCACGCCT[C/G]TAATCCCAGCACTTT	4799
rs529683698	snp	A/G	0.00386413	0.0437851	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33319060	AAGTAGTAGTCGGAA[A/G]ACATGCATGGACCCT	4799
rs529777331	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33356855	AATTAGCCAGGTGTG[A/G]TGGTGCACACCTGTA	4799
rs529792975	snp	C/T	0.00557542	0.0525036	intron-variant	NFX1	GRCh38.p7	9:33334017	AAGTACAGTGGCGCA[C/T]CCCTGTAATCCCAGC	4799
rs529828863	snp	A/C	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33304176	CTGAGGCAGGAGAAT[A/C]GCTTGAACCTGGGAG	4799
rs529831617	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33333559	TCTTCCTATGTAAGA[A/G]CAAGGAAAACAGTCC	4799
rs529865270	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33312022	CAGAGCCCACCCTTG[G/T]TCCATTATAATACAA	4799
rs529867014	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33303763	GAATATCTCAGTTCC[C/T]CCAAGTATTAGGGGA	4799
rs529895934	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33354705	CTGAAGAGCAGGTGG[C/T]CTCACAGGCTGCTTC	4799
rs529903358	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33311505	GAAGTTATATGCACA[A/G]TGAGATTGTGAGACT	4799
rs529914640	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33362086	AGATCATGCCACTGC[A/G]CTCCAGCCTGGGCAA	4799
rs529949611	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33319580	AGTGGTAGGATCTCA[C/G]CTCACTGCAGCCTCT	4799
rs529978224	snp	A/C	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33361662	CCTGTAATCCCAGCT[A/C]CTCGGGAGGCTGAGG	4799
rs530096574	snp	C/T	0.000399281	0.0141238	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33366712	CTTGGCCCAAGTTTA[C/T]GGCCTGGAGAGCGTG	4799
rs530128901	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33369097	TTGAGATGGAGTCTC[A/G]CTCTGCCGCCCAGGC	4799
rs530141781	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33325593	GGCATGAACCCGGGA[A/G]GCGTAGCTTGCAGTG	4799
rs530182967	snp	C/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33318041	GTTCTGTTTAATGTA[C/T]GATTTTATTTTATGA	4799
rs530190718	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33337519	CACCTTAAACACTAC[C/T]GTTGCTATTTTTTTT	4799
rs530220675	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33317390	CATGACTGCACTCCA[A/G]CCTGGGTGACAAAGT	4799
rs530259359	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33309730	ACTCCTGGGCTCAAG[C/T]GATCCTCCCACCTCA	4799
rs530272329	snp	G/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33339743	GGGAGTACAGGCATT[G/T]GGTATATACAGCCAT	4799
rs530285432	in-del	-/A	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33346514	ATGTGGCAGCAACCC[-/A]ATCTGCATAGGAACT	4799
rs530380363	snp	A/G	1.72124e-05	0.00293359	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294462	CTGAATTCATTCCTC[A/G]GGAGAAAAAAAATTC	4799
rs530389866	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33346342	CCATTTTCTTAAGTG[C/T]TTATTGTATTTCTAA	4799
rs530408352	snp	A/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33339021	TTAAAAAGATTTTTT[A/T]AAATAAAATATTTAT	4799
rs530449066	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33343404	GCGGATACTTGGTTT[A/G]ATAGAAGGTAGCTGG	4799
rs530472016	snp	C/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33340214	GACATCCAGGCATTT[C/G]CATACATCTTTTGAA	4799
rs530610576	in-del	-/CT			intron-variant	NFX1	GRCh38.p7	9:33306485	TTAGGTGGATTGCAC[-/CT]CTCAACATGAATAAA	4799
rs530611834	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33311349	TTAGAACAGGAAGGA[A/G]AGGACAGAAGGAAAG	4799
rs530647654	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33361525	CACCCGTAATCCCAG[C/G]ACTTTGGGAGGTCGA	4799
rs530650899	snp	A/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33338839	GAAGAGAAAGAGATA[A/T]GAGAAGGTCTCACAC	4799
rs530715862	snp	C/T	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33367799	TCCCACCAGAGGGGT[C/T]CTAAGTTTGTTGTTT	4799
rs530731601	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33303079	GATATGCTTAACATT[A/G]AAATTATTACCACTA	4799
rs530784044	snp	A/G	3.2969e-05	0.00405998	intron-variant	NFX1	GRCh38.p7	9:33367496	ACTTTTCAATGCTTG[A/G]TGTTTTGACTTTTAT	4799
rs530864065	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33365198	AGAATTCCTTGAACC[C/T]GGGAGGCAGAGGTTG	4799
rs530926285	snp	C/T	0.00159617	0.0282053	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33366119	CCTCCCTTCTGTTAC[C/T]ACTTCCCAGCAGAAT	4799
rs530933378	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33302932	CTCTGCTTCACAAAG[C/T]GCTGGGATTATAGGC	4799
rs530938010	in-del	-/TCT			intron-variant	NFX1	GRCh38.p7	9:33312504	GGGATGAAATAAAAC[-/TCT]TCTTGCAGGAGAGTA	4799
rs530968110	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33317344	ACATTGCTTGAGCCC[A/G]GGAGTTTGAGGCTGC	4799
rs530996121	in-del	-/T	0.00398564	0.0444627	intron-variant	NFX1	GRCh38.p7	9:33333552	GTTGTTCTCTTCCTA[-/T]GTAAGAGCAAGGAAA	4799
rs530997402	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33340721	ACCTCTTGAATGCTT[C/T]GCTACTTAGAAATTT	4799
rs531029054	snp	C/T	0.0023933	0.0345097	intron-variant	NFX1	GRCh38.p7	9:33301917	TCTCTACTAAAGATA[C/T]AAAAATTAGCCAGGC	4799
rs531030983	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33293552	GAAGTTAAAATAAGT[C/G]ATAAGTGACTTAAAC	4799
rs531040109	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33324061	AGCCTGAGCACGTAG[C/T]GAGACCCTATCTCTA	4799
rs531066480	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33369478	AAATGCCCATGTGCC[C/T]ATTACCAAATTTCAA	4799
rs531079827	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33360107	TCTCAGCTGCAGAAT[G/T]TAAATTAGGAGTCCT	4799
rs531208311	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33305562	ATTCTTTATGGAGAT[G/T]AGTTTGGTAGCAGTG	4799
rs531234975	snp	A/G	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33353030	TCACAGGCGTGAGCC[A/G]CTACACCTGGCTGGA	4799
rs531236858	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33345752	TTGAGTGTCCTGTTA[C/G]ATGGATGGGCCATAA	4799
rs531276678	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33315040	TCTTCCTCTCCATTA[A/C]TGCAATCTAGAAATG	4799
rs531285701	snp	G/T	0.00358779	0.0422022	intron-variant	NFX1	GRCh38.p7	9:33305938	CTAGCGGATGAAAGG[G/T]TACAGAGTGAGAAAA	4799
rs531341111	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33355115	TGTGTGGTTTTGGGC[A/G]TGATATAAACATCAC	4799
rs531387710	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33290892	GGGGCAGCGGCGCAC[C/T]GACCTTCGACAGGCG	4799
rs531395133	snp	C/G	0.00199481	0.0315187	intron-variant	NFX1	GRCh38.p7	9:33362370	AATCAACTGAAGTGG[C/G]CAACATGGCTGCATG	4799
rs531404652	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33321574	AAAGCTAGGGAAAAC[C/T]ATAAAAAAGCAACCA	4799
rs531404709	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33353028	GATCACAGGCGTGAG[C/T]CACTACACCTGGCTG	4799
rs531442809	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33328839	AAGGCAAATATACAG[A/G]TCACTCTACCAAATA	4799
rs531466619	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33297602	TCATCTGAGGCTCAG[C/G]GTTCTCTTTCAGTCA	4799
rs531488861	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33299639	GATGCAGTGAGCCAC[A/G]ATCATGCCACTGCAC	4799
rs531555790	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33340594	AGCCAGCTTGATTTT[C/T]TTCTCAGAAAATAGG	4799
rs531595030	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33306186	AGAGCCACTTTGTAG[A/G]AAAAATTGACACAAC	4799
rs531604802	snp	A/G	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33356848	AAAATAAAATTAGCC[A/G]GGTGTGGTGGTGCAC	4799
rs531631393	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33342573	ACCTCATGACGAATT[C/T]TGTTTTATCTTCATC	4799
rs531637205	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime, downstream-variant-500B	NFX1, LOC105376018	GRCh38.p7	9:33348382	TTTTAAAAACTACAC[A/G]TTGGGTACAATGTAC	4799
rs531669859	snp	A/C	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33303685	ATCAGATTTTTTATA[A/C]ACCAGCATTATAAAC	4799
rs531679531	snp	A/C	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33354618	CTGTCCTTCAGAGGG[A/C]CCTCATCCAGCCATT	4799
rs531686481	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33327051	ATTGACAAAATGCAA[A/G]TGAAAATAGGAAAGG	4799
rs531698326	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33347857	CTACTCAGCCAGGAA[C/T]GAAATAATGGCATTC	4799
rs531721503	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB	NFX1	GRCh38.p7	9:33289115	TTAGTCATCCCTCCT[C/T]TCCCCCTGCCTCCTG	4799
rs531857365	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33328235	TTTCACCATGTTCCC[A/G]GGTGATCTCGAGCTC	4799
rs531893166	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33334848	CATTATTAATAAGCA[A/G]GAACCGTCCTGTCCC	4799
rs531902847	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33341499	GGTAACACAGTACCA[A/G]TAGCAAGGTAGTACG	4799
rs531957048	in-del	-/A	0.00119737	0.0244387	intron-variant, utr-variant-3-prime	NFX1	GRCh38.p7	9:33348051	AGGCGGGTGAGGGAT[-/A]AAAAAACTACACACT	4799
rs532051465	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33334206	ACATCTGTAATCCTT[A/G]TGCTTTGGGAGGCCA	4799
rs532088645	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	NFX1	GRCh38.p7	9:33289822	CCTCTTTCACGCAGG[A/G]CAGGCTGCCCACCCT	4799
rs532096726	snp	A/T	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33322696	ACTATCCCACCCAGC[A/T]CCCAGAGTAGTGCCT	4799
rs532139295	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33355420	TAGATTAGTTTTTGA[A/T]CTTTATGTAAGTGAT	4799
rs532147014	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33300096	TTTTTTTTTTTGAGA[C/G]GGAGTCTCACTCTGG	4799
rs532168795	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33297472	GAATTATCACAATGT[A/G]GTGGCTTATGATAAC	4799
rs532189373	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33367962	CTCTGGGCCGGGCGC[A/G]GTGGCTCACGCCTGT	4799
rs532213594	in-del	-/CCT			intron-variant	NFX1	GRCh38.p7	9:33327446	CTTGGCTCACTGCAA[-/CCT]CCGCCTCCCAGGTTC	4799
rs532223590	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33328098	TCACTGTAGCCTCAA[C/T]GTCCCATGCTCAGGA	4799
rs532258603	snp	A/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33334782	GATCTGCCTTGTCAT[A/T]GTTCACCATGACCCT	4799
rs532308622	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33312085	ATAGCTGTGGAGTGT[C/T]TCTGAGGCCCAGTAA	4799
rs532387317	snp	A/C	0.000399281	0.0141238	intron-variant, downstream-variant-500B	NFX1, LOC105376018	GRCh38.p7	9:33348978	ATAACAACATGCTAT[A/C]TTCTTTTATCTTCAT	4799
rs532398279	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33362788	AGCTCACTGCAAGCT[C/G]TGCCTCCCGGGTTCA	4799
rs532403985	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33312730	ACAAAAATTGGCTGG[G/T]TGTGGTGACACGTGC	4799
rs532435433	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33360793	GATCTTCCCCTAGAA[A/G]TTCTCTTGAAAATTT	4799
rs532450684	snp	A/G	0.00119737	0.0244387	intron-variant, utr-variant-3-prime, downstream-variant-500B	NFX1, LOC105376018	GRCh38.p7	9:33348566	AATGAAAAAGTCTGA[A/G]ATGTTGCGAGAATTA	4799
rs532451581	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33342130	CTGTCTCTCTCTCTC[A/T]CACACACACACACAC	4799
rs532468442	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33310486	ATATAGCTCCTAAAA[C/T]AGCATTTTTCAGAGG	4799
rs532512139	snp	C/T			intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33365725	TGACTGTGTGGGACA[C/T]TTAGGAAGACACTCT	4799
rs532573361	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33306779	TTATGTCCTTTCCAT[G/T]TCTTACTGCCTCCCC	4799
rs532582366	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33302933	TCTGCTTCACAAAGC[A/G]CTGGGATTATAGGCA	4799
rs532613132	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	NFX1	GRCh38.p7	9:33289030	TGTCTTCCTGGCCGG[A/G]GCCTGGCACCTTAGC	4799
rs532635697	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33304453	TTATTTTTCTAACCA[A/G]TTTGCTCATATTTCT	4799
rs532657490	snp	C/T	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33309383	AAAAAAACTTAATCC[C/T]CTGCATGGACTATTT	4799
rs532683000	snp	C/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33340400	CAGGGCACCAAGTCC[C/T]GAGGCTGCATGCAGC	4799
rs532802978	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33334099	GCAGTGAACTGAGAT[C/T]ACACCATTGCTCTCC	4799
rs532830518	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33357693	CACACCACTACGCCT[A/G]GCTAAGATTTTCTTT	4799
rs532863696	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33339800	AAAGGGGCTACAGGC[C/G]CCATGCAAGTCCGAA	4799
rs532870223	in-del	-/TG	0.00159617	0.0282053	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33366218	CTCTGCTTGTGTGTC[-/TG]TATCTGAATACTCAC	4799
rs532922880	in-del	-/CTTTATATAC	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33353104	AAAGAAACAGTGCTG[-/CTTTATATAC]CTTTTCTTCCCTAAC	4799
rs532923806	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33292375	TTTCTGCCGGTGAGC[A/C]GACTCTGCAATGCCA	4799
rs532939688	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33291797	AGTCCCAGCTACTCC[A/G]GAGGCTGAGGCAAGA	4799
rs532949944	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33300239	CCAGCTAATTTTTGT[A/G]TTCTTAGTAGAGATG	4799
rs532978433	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33299198	GCACTGGTATAATCA[C/T]ATTAACTAAACTACA	4799
rs533097210	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33337046	GGCGGAGGTTGCAGT[A/G]AGCAAATTTTTGTAG	4799
rs533108489	in-del	-/GGGCAGGGCA	0.00517822	0.0506191	upstream-variant-2KB	NFX1	GRCh38.p7	9:33288543	CAGCTCCTGGGGGCT[-/GGGCAGGGCA]GGGCAGGGCAGGGCA	4799
rs533203529	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33329067	TTACACTCATGGTTA[G/T]AGCTTTACTACAAGG	4799
rs533218594	snp	A/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33292706	CATATCCTGTATATG[A/T]GTACATGCAGCCTTC	4799
rs533290065	snp	A/G	0.00199481	0.0315187	intron-variant	NFX1	GRCh38.p7	9:33342441	CACTCCAGCCTGGGC[A/G]ACAGAGCGAGACTCC	4799
rs533356205	snp	A/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33363809	GACTTGCTCAGATCC[A/T]TATAGATCTGTTTAT	4799
rs533377555	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33357107	ACAAGGTCAGCAGAT[C/G]GAGACCATCCTGGTA	4799
rs533394548	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33314176	TTTAGTAGAGATAGG[A/G]TTTCACAATGTTGGC	4799
rs533414802	snp	C/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33336372	AGGTGCCCGCCACCG[C/T]GCCCGGCTAATTTTT	4799
rs533451901	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33343143	GGTTCTGTCCTCAAC[A/G]ATCTTCTTTCTCTAT	4799
rs533455322	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33329720	ATGGAGTGCAGAGGC[A/G]CAGTCTTGGCTCACT	4799
rs533565974	snp	C/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33370490	CCATATCCGGAATCA[C/G]ACATGTTATCTTAAA	4799
rs533604861	snp	C/T			intron-variant, utr-variant-3-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33347872	CGAAATAATGGCATT[C/T]ACAGCAACCTGGATG	4799
rs533701341	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33322186	AGCCTAGGTGACAGA[A/G]TGAGACTCCATCTCG	4799
rs533722825	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33369546	ACAAGTGAGATGCTC[A/G]CTTGGCTTAAGCTGT	4799
rs533730446	snp	A/C	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33335379	GGAATTACAGGCACC[A/C]ACCACCATGCCTGGC	4799
rs533832287	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33314549	GGGCGTGGTGGTGGG[C/T]GCCTGTAATCCCAGC	4799
rs533878105	snp	C/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33304646	TTACAAAGGAAGCTT[C/T]CCTTTGTTATTCTCT	4799
rs533892040	snp	A/C	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33327456	TGCAACCTCCGCCTC[A/C]CAGGTTCAAGCGATT	4799
rs533928369	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33329847	TATTTTTAGTAGAGA[C/T]GGGATTTTGCCATGT	4799
rs534019262	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33334350	TAGTCCTAGATACTC[A/G]GGAGGCTGAGGCAGA	4799
rs534044188	in-del	-/AAAAC	0.00119737	0.0244387	intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33351446	GAAACCCTATATCCG[-/AAAAC]AAAACAAAACCAAAC	4799
rs534051912	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33323759	CTTCATCTCAAAAAA[A/C]AAAACAAACAAAAAA	4799
rs534052668	snp	A/C	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33333868	CATAATTTGGGTCCA[A/C]GCCTGGTGGCTCATG	4799
rs534145504	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33345401	AGAATCACTTGAACC[C/T]GGGAGGCAGAGGTTG	4799
rs534149506	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33355757	TCAAGCGATTCTCTT[C/G]CCTTAGCCTCCAGAG	4799
rs534198170	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33351186	GTTATTGCCAGATGC[A/G]GTGGTTCACACCTGT	4799
rs534199768	snp	C/G	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33326128	AATTTTGTATAAGAG[C/G]GGGGCTAGGCGCAGT	4799
rs534236681	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	NFX1	GRCh38.p7	9:33289232	AGACCGGGGCTCCAG[C/T]CAGACCCCCGAAAGG	4799
rs534399667	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33331485	CCACTCCTGCATATC[A/G]TTTCTTCCATATAAT	4799
rs534413675	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33328078	TTCAGTGGTGCGATC[A/G]CAGTTCACTGTAGCC	4799
rs534434786	snp	C/T	0.0023933	0.0345097	intron-variant	NFX1	GRCh38.p7	9:33330691	CTCTTTCTATCTCTA[C/T]GTTTTCTTGCTTCTC	4799
rs534435151	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33337688	GAGCTATGTTAATGC[C/T]ACTGCACTCCAGCCT	4799
rs534437549	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33312415	TTAGCCATTATGTCA[A/G]GTACTGCAAGCTGAT	4799
rs534437567	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33303981	TATTCAGAAATTACC[A/G]ATGGGCCGGGCTTAG	4799
rs534481108	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33320875	TCTTTCAAGTGCCAG[C/T]GTGAATCAGTGGGAA	4799
rs534500200	snp	A/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352100	TGTCTTTTGTGCAAG[A/T]CATAGTATGAGGTGC	4799
rs534558353	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33359075	CTTATTTAGCAACCT[C/T]GCTAAATTCACTTAT	4799
rs534629846	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33365358	CACCTGTAATCCCAG[C/T]GCTTTGGGAGGCTGA	4799
rs534638969	in-del	-/TTTTTCAGATTTTGTTTC	0.00199481	0.0315187	intron-variant	NFX1	GRCh38.p7	9:33303880	CCCTCTAGTTGTTGA[-/TTTTTCAGATTTTGTTTC]TTTTTCAGATTTTGT	4799
rs534662175	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33324252	GGTGTGGCGGCACAC[A/G]CCTGTAATCCTGGCT	4799
rs534736328	snp	C/G	0.00478085	0.0486577	intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33350290	GCCTGGGCGACAGAG[C/G]GAGACTCCATCTCAA	4799
rs534737468	snp	A/C	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33306408	CAGACATTTGGACAT[A/C]TGGGTCTGAAACTGA	4799
rs534742714	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33339813	GCCCCATGCAAGTCC[A/G]AAATTCAGTGGGGCA	4799
rs534768756	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33334300	TCTTTGCAAAAGAAT[G/T]TTTAAAGTTAGCCAG	4799
rs534799507	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33308331	CCTGTAGTCCCAGCT[A/G]CTTGGGAGGCTGAGC	4799
rs534856121	snp	C/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33309083	TTAATCCTGGCTGGG[C/T]GCGGTGGCTCATGCC	4799
rs534872188	snp	C/T	0.00716266	0.059414	intron-variant	NFX1	GRCh38.p7	9:33337941	GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG	4799
rs534926637	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33316630	TTATCTTCTTGAATT[A/G]TAATCTTCTAGGATC	4799
rs534957501	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33369224	GCGCCTGCCACCACG[C/T]CCGGCTAATTTTTTG	4799
rs535006864	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33357250	GAGCTTGCAGTGAGC[C/T]GAGATGGTGCCACTG	4799
rs535070978	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33363907	TTACCAAAATAGAGA[G/T]AAATAATGTGTAAAG	4799
rs535098009	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33314904	GAATATGTAAAATAT[C/T]TGTGTTTATTATATG	4799
rs535099134	in-del	-/T	0.0159988	0.0879968	intron-variant	NFX1	GRCh38.p7	9:33338479	ATATCCTTTGTCTGG[-/T]TTTTTTTTTCTTTTT	4799
rs535133206	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33322887	GCCATCTAGTTCATC[A/G]GAGAGAATCAGGGAA	4799
rs535136647	snp	G/T	0.000132002	0.00812304	intron-variant	NFX1	GRCh38.p7	9:33367476	CATCTCCACAAACAA[G/T]TCTCACTTTTCAATG	4799
rs535168647	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33337152	TTAAATTTTCGATAG[A/G]AACACACTCAGCCAG	4799
rs535192468	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33330040	CTCAGGTAATCTACC[C/T]GCCTCAGCCTCCCAA	4799
rs535202185	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33344271	CTGTCTTCACTGCTC[C/T]AGAGTCATGCTGTGA	4799
rs535258559	snp	G/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33365284	TGTCTCAAAAAGAAA[G/T]AAAGAAAGAAAGAAA	4799
rs535279669	snp	G/T	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33358170	CGTTCTGTTTCCCAG[G/T]CTGGAGTGCAATGGT	4799
rs535325338	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33344304	GCTGCCCCTTGCTCC[C/T]GGCTCAGGGGCTGGT	4799
rs535392939	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33341539	ATGTATATAGCATAC[A/C]TAATTATTTTTTAAA	4799
rs535407244	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33364628	TGTCTATTGTCTACG[C/T]TTTACAGGGAGAGGA	4799
rs535504131	snp	A/G	0.00676609	0.0577691	intron-variant	NFX1	GRCh38.p7	9:33356568	GTCCTATTTAGAAAA[A/G]TTTGTCTATCCTGAG	4799
rs535533544	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33321906	AAAAATCAACCATTT[A/G]AAGTTTCTGGAGGCT	4799
rs535619735	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33343758	AAATGTTGATAAATT[G/T]CCTATTATAATATTA	4799
rs535712184	snp	A/C	0.000399281	0.0141238	intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33349488	ACTAAAATATGGATT[A/C]CAGTGCGATGGGAAA	4799
rs535723232	snp	G/T	0.00199481	0.0315187	intron-variant	NFX1	GRCh38.p7	9:33315787	GTCCTAGCTACTTGG[G/T]AGGCTGAGGTGGAAG	4799
rs535737981	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33298022	ACACTTCATTCATAT[C/T]TGTTGCATAAATACT	4799
rs535754579	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33314247	GCCTGGGCCTCCCAA[A/G]GTGCTGGGATTACAG	4799
rs535759013	snp	C/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33323701	GAGGTTGCAGTGAGC[C/T]GCGATTGCGCCACTG	4799
rs535776112	snp	C/T	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33305927	TAGTTAAGACCCTAG[C/T]GGATGAAAGGGTACA	4799
rs535843963	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33369037	ACCATGTGGAGTTAT[C/T]GGCCCGTTTATCCCA	4799
rs535870048	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33363862	ACCTCATGTCCCAAG[C/T]TGTTGTTATTCTCTC	4799
rs535881262	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33309756	CCTCAGCCTCCCAAA[G/T]TGCTGAGAGTACAGG	4799
rs535982256	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33325829	GCAAGTAAACCCAAA[C/T]AGAATTTCAAATCCA	4799
rs536005761	snp	C/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33339928	GGTCTTGGACAGCTC[C/T]GCCCATGTGGCTTTG	4799
rs536026281	snp	C/T			intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33349599	AGGGTTCAAGACTAG[C/T]CTTTGGTCCTACGAG	4799
rs536045347	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33350220	GAGGTAGGAGAATCG[C/T]TTGAACCCAGGAGGT	4799
rs536051811	snp	A/T			intron-variant, utr-variant-3-prime, downstream-variant-500B	NFX1, LOC105376018	GRCh38.p7	9:33348359	TCCGTCTCGAAAAAA[A/T]AAATAAATTTTAAAA	4799
rs536055820	snp	G/T	0.00199481	0.0315187	intron-variant	NFX1	GRCh38.p7	9:33291365	TGAGGTTGGTTGGTT[G/T]GTTTTACAATCAGCA	4799
rs536082753	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33298801	AAAAAAAAATATTAT[C/T]AAGCTGCTGTGTGGA	4799
rs536085796	snp	G/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33295687	AGGAATTTTGTAAGG[G/T]TTTTCAAAAATGCAA	4799
rs536103561	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33357219	AGGCAGGAGAATGGC[A/G]TGAACCCAGGAGGCG	4799
rs536120483	snp	C/T	0.000378922	0.0137593	intron-variant	NFX1	GRCh38.p7	9:33303181	GGCCTACTCCCATTT[C/T]TCCTGACAGATGGCC	4799
rs536239699	snp	A/G	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33293749	AGGGGAGTATGCTTA[A/G]TTTTTTCCACTTTGG	4799
rs536240179	snp	A/G	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33360502	TTTGAATTTCTCCTC[A/G]ATCTTGGTGATGACA	4799
rs536249406	snp	A/T	1.65952e-05	0.00288051	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352770	AGGTGAAACAGATAC[A/T]TGTGTTTTGTTTTGT	4799
rs536318776	snp	G/T			missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33303241	AATGTTTCTGCACAT[G/T]TTCCTAATACCTACA	4799
rs536507775	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33339091	CTGGCTATTTGTACT[C/G]TGTTATCTCATATAC	4799
rs536508279	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33346601	TCATTGTAGGAGGTG[A/G]GTTTTGATGAACCTC	4799
rs536511924	snp	C/G/T	0.000115688	0.00760465	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294993	GAACAACTCCAAAAC[C/G/T]GGAGGATGCTGGACC	4799
rs536548888	snp	C/T	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33302459	CTTGAATTCCTGGAC[C/T]CAAATGATCCTCCTG	4799
rs536614042	snp	A/C	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33337789	CATGGTGGTTCACAC[A/C]TGTAATCCCAGCACT	4799
rs536649619	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33345212	CCGGGTGCAGTGACT[C/T]ACACCTGTAATCCCA	4799
rs536731655	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33325123	AAAACTTTCAAATGT[A/G]TTGAAAAACACTACA	4799
rs536766440	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33332406	TGTTACCTATGGCAT[C/T]ATATTATAGTTGTAT	4799
rs536769820	snp	A/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33324521	ATGCCACTGCGCTTC[A/T]GGTGGGCAAGAAAGC	4799
rs536843599	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33353289	TTGACACAGCCAGGG[C/G]TAAGCTCTGTGCTCC	4799
rs536885656	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33302397	GACAGAGTCTTACTC[G/T]GTTACCCAGGCTGGA	4799
rs536921183	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33309576	AAGCCCATTCCCCAG[C/T]AGCACTTTTCTGGTC	4799
rs536955112	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33318489	CACTATGAGATATTA[A/G]TAGTTTAACAAGGCT	4799
rs536973202	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33338311	AGTGAGCCGAGATCA[C/T]ACCACTGCACTCCAG	4799
rs537043951	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33358863	CACACCCAGCTAATT[G/T]TTTTGTTTTTTTTTT	4799
rs537079566	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33299917	AGGAGAGCCAATATT[A/G]TGGAATATTACAGTG	4799
rs537102272	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33299191	GAAATTAGCACTGGT[A/G]TAATCATATTAACTA	4799
rs537178341	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33305302	GAATTGAACTGGCAT[C/T]GTAAACTAGGTAAAA	4799
rs537205229	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33338289	GAACCTGAGAGGTGG[A/G]TGTTGCAGTGAGCCG	4799
rs537298831	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33363941	TTAGGATATAGTAGG[C/T]ACTCGGGGTTACTGC	4799
rs537313079	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33333000	ACAGGTGTCCACCAC[C/T]ACACCTGGCTGATTT	4799
rs537324606	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33301667	CTCTTATTGAAAATG[A/G]TGGCTTTTACTTATT	4799
rs537361165	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33360277	ACAAATCACTTAGCT[A/G]TGAGACCTTGGGCAA	4799
rs537446413	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	NFX1	GRCh38.p7	9:33289456	CAGGAGGTGGTGCCC[C/T]CTGGCTCCTGGGACT	4799
rs537454927	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33292382	CGGTGAGCAGACTCT[A/G]CAATGCCAGCCTTGT	4799
rs537485251	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33296589	AAAATAAAAAAATTA[A/G]CCAGGCATGTTAGCA	4799
rs537506788	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33358126	ATTTTTCTTGTATTA[C/G]TTGTAATTTTTTTTT	4799
rs537509391	in-del	-/T	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33307971	ACCACGCCTGGCTAA[-/T]TTTTGTATGTTTTGG	4799
rs537514081	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33323241	CACTGAAATAGTCTA[A/G]CCAAGTCACAAAACA	4799
rs537516260	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33303910	TTTCTTTACTGTCTG[C/T]CTCCCTCCCTGAAGC	4799
rs537555134	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33311657	GCCTGGGTTCAAGCA[A/G]TTCTCCTGCCTCAGC	4799
rs537597362	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33328464	TGCATACTTCCCTCA[A/G]CTCTGATTCTGGAGT	4799
rs537640175	in-del	-/TATA	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33341526	ACGTGTGTATGTATG[-/TATA]TATATAGCATACATA	4799
rs537652602	in-del	-/T			intron-variant	NFX1	GRCh38.p7	9:33302677	TTTTGTTTGTTTTTG[-/T]TTTTTTTTTTGAGAG	4799
rs537711751	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33315071	GAACAGAAGAATCTA[A/G]TTTTATAGTTGGGGC	4799
rs537742859	snp	A/G	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33335275	TGCTCTTGTTGCCCA[A/G]GCTGGAGTGCAGTGG	4799
rs537743583	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33337772	AAAAACTGATGGCCG[A/G]GCATGGTGGTTCACA	4799
rs537749150	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33293605	ATTTATAGTATATTC[G/T]GTATGCTACACATAG	4799
rs537807649	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33341191	GGACTTACAGTTCCA[A/G]GTGGCTGGGGAGGCC	4799
rs537842430	snp	A/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33355622	TGTTAGACTATTACA[A/T]ATAAAACTGTTAAGA	4799
rs537844477	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33356301	GTGCCTGTACAAGTC[C/T]TTTGCTTATTTTTTT	4799
rs537873797	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime, downstream-variant-500B	NFX1, LOC105376018	GRCh38.p7	9:33348576	TCTGAGATGTTGCGA[A/G]AATTACCAAAATGTG	4799
rs537884611	snp	A/G	0.00358779	0.0422022	intron-variant	NFX1	GRCh38.p7	9:33304302	ACAAAGAAATCACCA[A/G]TGACTCCTTTCCAGC	4799
rs537903515	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33354290	ATAGTAGAGCCTTGC[A/G]TACACAATAAGTATT	4799
rs537917797	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33347296	TTTACCCTTTTTATT[G/T]TACAGATCCATGAGT	4799
rs537954303	in-del	-/TC	0.00199481	0.0315187	intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33349712	TTCTATCCCCTGTTG[-/TC]TCTTAATTTTTTAAA	4799
rs537970196	snp	C/T			intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33350424	TCTATTGACTCTGCT[C/T]TAGCAGTTCAGAAAG	4799
rs537978658	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33319833	AAAATTGTAAGTACA[A/G]TAGAACCTCAGCCAT	4799
rs538000967	snp	A/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33335856	AAGTTTATCATACTG[A/T]AGTATATATCAGCAC	4799
rs538049443	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33368862	TCAGACTCAGCCAAG[A/G]GCGTCCTGGTCCCCA	4799
rs538129310	snp	A/C	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33300747	TTATGGTAGGCACCA[A/C]GAATATCTTTGTTAA	4799
rs538172454	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33341767	AAACCCCATCTCTGC[C/G]AAAAATACAAAAATT	4799
rs538191713	snp	A/C	0.234109	0.249494	intron-variant	NFX1	GRCh38.p7	9:33367697	ATTGTCCTGAGCTGC[A/C]CCAGCCATTGGTGGC	4799
rs538242815	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33295766	AAACAAGTGGTGGGT[A/G]GTAACATCTCTGCTG	4799
rs538242882	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33303879	TTCCCTCTAGTTGTT[G/T]ATTTTTCAGATTTTG	4799
rs538253413	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33314362	ATTATTATGGACCTA[A/G]AAAGACCAAAATAAT	4799
rs538279926	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33303332	CCTCAGTTCAGGAAA[A/G]GTGGTCTGCGGGGCA	4799
rs538301509	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33295552	AAAAAGTCTCAATCT[C/T]TATTCACTGTCTGCC	4799
rs538320728	in-del	-/T	0.0159988	0.0879968	intron-variant	NFX1	GRCh38.p7	9:33338478	ATATCCTTTGTCTGG[-/T]TTTTTTTTTTCTTTT	4799
rs538325359	snp	A/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33310821	GGGCCAAGACTGTAT[A/T]TGAAAATGTCATCTT	4799
rs538359378	in-del	-/T	0.0166325	0.0896639	intron-variant	NFX1	GRCh38.p7	9:33323920	CCCAAATGGAAATTC[-/T]GAAGTTTAAAAGTAG	4799
rs538365917	snp	C/G/T	0.000164993	0.00908137	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33319113	GCGGCAAGCCTCTGC[C/G/T]TTGTGGTTCCTTAGG	4799
rs538406640	snp	A/C	0.0023933	0.0345097	intron-variant	NFX1	GRCh38.p7	9:33334467	CTCTAAAACAATAAA[A/C]CAAAATAATAAAAAC	4799
rs538417032	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33361225	ATGAGCCATGAAGAC[A/G]GTTAAGTGTGAAAAC	4799
rs538487021	snp	A/G	0.00279162	0.0372561	intron-variant	NFX1	GRCh38.p7	9:33319802	GGTGTAAGCCACTGT[A/G]CCTGGCCAAAGAACT	4799
rs538488506	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	NFX1	GRCh38.p7	9:33289331	CTCACCCCCACCCCC[A/T]TGTCCTGGGTAGGCC	4799
rs538502202	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33296477	TCACACCTGTAATTC[C/T]TGCACTTGGGGAGGC	4799
rs538522981	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33327446	CTTGGCTCACTGCAA[C/T]CTCCGCCTCCCAGGT	4799
rs538522998	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33319188	GGTTGGCAGCAGTGA[A/G]TGTTTAAGCAATGTA	4799
rs538554526	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33341006	TCTGAGCCCTCCAGA[C/G]TGTTCCAACATCTGC	4799
rs538578196	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33353846	GGCACCTGCTACCAT[C/G]CCTGGCTAATTTTTT	4799
rs538615640	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33339301	ATCATGGTGGAAGGC[A/G]AGGAAGAGCAAGTCA	4799
rs538616027	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33312707	GAAACCCCGTCTCTA[C/T]TAAAAATACAAAAAT	4799
rs538630660	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33354367	CCTACTCAGGAGATG[A/G]CTAAGACTAAAGGAG	4799
rs538667483	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33354734	TCCTGGCCTGAGGGA[C/T]TGTTTTTTGGCAAGA	4799
rs538693526	snp	A/C	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33361205	GGGAACATAATTAGA[A/C]GACTATGAGCCATGA	4799
rs538698533	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33329442	CTGCTCCTAAATCAC[A/G]TAATTGGACTATCCA	4799
rs538701573	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33296546	CAGCCTGGGCAACAT[A/G]AGGAGACCCTGTCAC	4799
rs538727608	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33353892	ACGGGGTTTCACCAT[A/G]TTGGCCAGGCTGGTC	4799
rs538758134	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33346447	CGAGAGGAGGAGGAC[A/G]GTAGTTCAATACACA	4799
rs538763675	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33292883	CAATACCCACTGGTC[C/T]AATTTAACCATTCCA	4799
rs538820715	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	NFX1	GRCh38.p7	9:33289972	AACCATGAGAATATC[A/G]GTGATACTGATGAGA	4799
rs538958581	snp	A/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33340068	AGGACAGTGGCCTTC[A/T]TCTCACAGCTCCACT	4799
rs538976861	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33302815	GCTGGGATTACAGGC[A/G]CGCACCACCACGCCC	4799
rs538994604	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33332684	TTGATGAAATGCTGA[A/G]AAATATAAGCTAAGT	4799
rs539039928	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33313310	GAAGAAAGAGTGGGC[C/T]GGGCGTGGTGGCTCA	4799
rs539113210	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33350054	CATGCCTGTAATCCC[A/G]ACACTTTGATAGGCT	4799
rs539118879	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33290710	TAGCACATGCTAGGG[C/T]GTAGGATAGTGGCTC	4799
rs539122106	snp	G/T	0.0089031	0.0661233	intron-variant	NFX1	GRCh38.p7	9:33338478	CATATCCTTTGTCTG[G/T]TTTTTTTTTTCTTTT	4799
rs539141567	snp	A/G	1.64751e-05	0.00287007	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33301333	ATTGGTTCGTGTCAC[A/G]GCCCCAGTGTGGAGT	4799
rs539156873	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33336238	TTTGTTTTTTTGAGA[C/T]GGAGTCCCACTCTGT	4799
rs539191403	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33342966	CTTGAACTAAGCCTT[C/T]GTATTTCCAATATGT	4799
rs539254224	snp	A/C	0.00358779	0.0422022	intron-variant	NFX1	GRCh38.p7	9:33360613	TCTAAAGTTATATCT[A/C]TATATACACACACAT	4799
rs539303858	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33314976	ATGAATAGAAAAAAA[G/T]TTTTTAATTGTGAAT	4799
rs539325036	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33326058	TAGAATAAGAAAATG[A/G]TACCAGATCACAACT	4799
rs539327065	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33333672	AAGGTACACAACATC[C/T]ACCCCTGGAACTGAG	4799
rs539362931	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33333095	AAGTGATCCACCCGC[C/T]TCGGCCTCCCAAAGT	4799
rs539377627	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33336558	CTAGTGAAGTGATAT[A/G]TCACTACCACATGAT	4799
rs539429569	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33368753	AAACCTCTGAAGGGT[A/G]GTTACGGCAGTTCAC	4799
rs539495579	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33298708	AGGATCGCTTGAGCC[C/T]AGTGGGTCAAGGCTG	4799
rs539532978	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33328346	TGACTTAGGCAAATC[A/G]TCGTATACTTTAAAG	4799
rs539569399	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33327521	AGGTGGGCGCCACCA[C/T]GCCTGGCTAATTTTT	4799
rs539639420	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33356514	TTTTAATGTTAATAT[C/T]ATCCAGTTTATTTGA	4799
rs539674978	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33349360	TAACATCCTAAAGGA[C/T]AGTGAGAAGAAAGTA	4799
rs539685424	in-del	-/TCT			intron-variant	NFX1	GRCh38.p7	9:33301780	TTTAATTTATCTTCT[-/TCT]CATTTTTGGCCAGGC	4799
rs539752359	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33312452	TGTACATAACAGTGA[C/G]TTTTAAAAACAAAAT	4799
rs539755129	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33321862	CCAGCTAGGCTGACA[A/G]AGTGAGACCCTGTCT	4799
rs539837386	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33369298	TCAATCTCCTGACCT[C/T]GTGATCCGTCCGCCT	4799
rs539853258	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33368262	GAATAGTTACTCTGA[A/G]GATGCAAGTGGGTGT	4799
rs539955969	snp	C/G	0.00914312	0.0669923	upstream-variant-2KB	NFX1	GRCh38.p7	9:33289005	CCACGGTCTGCTGGG[C/G]TCTTGGCACTGTCTT	4799
rs539964299	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33368103	AGCCGGGTGTGGTGG[C/G]GGGCACCTGTAAACA	4799
rs539992563	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33312699	AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAT	4799
rs540032258	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33323650	CCCAGCTGCTCCGGC[A/G]GCTGAGGCAGGAGAA	4799
rs540078599	snp	A/G	0.00557542	0.0525036	intron-variant	NFX1	GRCh38.p7	9:33363020	AAGTTCTCGTGTTCT[A/G]TGGCACACTGGGGTG	4799
rs540121095	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33312026	GCCCACCCTTGTTCC[A/G]TTATAATACAAGGTC	4799
rs540138893	snp	A/G			intron-variant, downstream-variant-500B	NFX1, LOC105376018	GRCh38.p7	9:33348875	CATTCCAACTGTCCT[A/G]TACCAAAAAAAAAAA	4799
rs540179713	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33320461	GCAGTTTGAATTGTT[A/G]TATCTGCTTGTTGAA	4799
rs540209220	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33360708	AACCTAGCAGGCCAA[A/G]TTCAGCCCACAGACA	4799
rs540209370	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33367723	GTGGCCTCCTCAGGC[C/T]TGGCCTTGGGGTACC	4799
rs540247202	snp	A/C	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33361404	TAAATCAAGCTAATT[A/C]GCATATGCATTACCT	4799
rs540275778	snp	C/T			intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33351094	GGTTGCAGTGAGCCC[C/T]GAGATTGGCGCCACT	4799
rs540328123	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33296695	AGCTATTGTACTCCA[A/G]CCTGGATAACAGAGC	4799
rs540329512	snp	C/T			intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33349532	GATGTTGGAAGTCTC[C/T]TCAGGGGGAGAAGTT	4799
rs540329722	snp	A/G	0.00517822	0.0506191	intron-variant	NFX1	GRCh38.p7	9:33334713	TAATATCTCAAAGAC[A/G]TATTTCCATGTCAGT	4799
rs540367440	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33341258	CATTTTAACATGGAT[A/G]GCAGCAGGCAGAGGG	4799
rs540397222	snp	G/T	0.0023933	0.0345097	intron-variant	NFX1	GRCh38.p7	9:33298324	GAGCAAATTTAGATG[G/T]GGGGAGGGGTATTAT	4799
rs540405716	snp	A/G	0.00318978	0.0398085	intron-variant	NFX1	GRCh38.p7	9:33362691	GTAATAAGTTCCTGT[A/G]GTTTTTTTTTTTTTT	4799
rs540442611	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33356046	TTATGTGTGTTCAGC[A/G]TTAGTAGATTCTGCC	4799
rs540459449	snp	A/G	0.000399281	0.0141238	intron-variant, missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33347729	AAGATACCTGCACAC[A/G]CATGTTTATAGCAGC	4799
rs540510906	snp	C/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33296075	GGGATTACAGGCGCC[C/T]GCCACCATGCTTGGC	4799
rs540512055	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33321276	GTTAAGGGATAAGAG[A/G]GTACCTGCTATACCT	4799
rs540535619	in-del	-/T	0.0146672	0.084371	intron-variant	NFX1	GRCh38.p7	9:33341872	CTGTAATCCCAGCAC[-/T]TTGGGAGGCAAAGGC	4799
rs540547207	snp	C/G	0.000296506	0.0121723	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33328625	CATGAAGGAGACTGT[C/G]GACCATGCTCTCGCA	4799
rs540559058	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33368907	CCACTCCTGGGAGCC[A/G]GGTGTCCTAGGTTCT	4799
rs540568264	in-del	-/TA			intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33350855	TAATAATCCTTATTT[-/TA]AAAACTGAGCTGAGT	4799
rs540587017	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33310439	TGAATATACAAATTC[C/T]GTATTGTAACTTTTT	4799
rs540637892	snp	C/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33353811	CTCCTGCTTCAGCCT[C/T]CTGAGTAGCGGGGAT	4799
rs540641749	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33358200	TGTGATCTCGGCTCA[C/G]TGCAAGCTCCACCTC	4799
rs540648907	snp	A/C/T	8.56679e-05	0.00654431	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33364765	AACCCTCGTGGAGGC[A/C/T]GTGAATAAGGTTGAA	4799
rs540716292	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33315973	GTATTGTTCGAAACT[C/T]GGTGTTCTTTGAGTA	4799
rs540737765	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33336349	GCCTCCCGAGTAGCT[G/T]GGATTACAGGTGCCC	4799
rs540770719	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33364230	TTTGTTTGTTTATCT[A/G]TTGTAAGAGATTATG	4799
rs540802844	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33297121	TTCTCACAGCTCCCC[A/C]TCTCCTTACTGCAAA	4799
rs540803988	snp	C/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33340241	TGAAACCTAGGCAGA[C/T]GTTTCCAACCTCAGT	4799
rs540881093	snp	C/T	0.000798403	0.0199641	intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33351255	TTCCACTCAAGAGTT[C/T]GAGACCAGCCTGGGC	4799
rs540910181	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33303472	TTCTGGAGATGGCCA[A/G]CCAGGCTCATGCTGC	4799
rs541019118	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33333336	TTTTACGATAAGGGT[A/G]TTTACTGCCACACCT	4799
rs541029134	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33333746	TTGCCTGAAAGAGAA[G/T]AGTGGCCGTTTGGGA	4799
rs541052328	snp	A/G			intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33366252	TTTTTAAAGTAGAAC[A/G]TACTTTTAAAGGAAA	4799
rs541074005	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33306721	AAGGTCTTTTATGCC[A/G]ACTTTATAGTTCTGG	4799
rs541076947	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33342318	TACAAAAAAATTAGC[C/T]AGGCATGGTGGTGGA	4799
rs541082345	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33360350	AAATGATGACAATAA[C/T]AGTATTTACCTTCCA	4799
rs541105883	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33306093	GCAAAAAAGCACAGA[A/G]GCAGGGAGGCTTTTG	4799
rs541109657	snp	G/T	0.000399281	0.0141238	utr-variant-5-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33290510	CGCCGGAAGTCCGGG[G/T]CACGTGACCTGGTGA	4799
rs541146496	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33297419	GAGTTGTTACTGAAT[C/T]CTTAAGGCTGGTTAA	4799
rs541187680	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33330268	ACAGAATTGTGAACC[A/G]TTGGTTCTGTTAAAC	4799
rs541198497	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33337514	CTCCACACCTTAAAC[A/G]CTACCGTTGCTATTT	4799
rs541230510	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33344717	CTAAAAATACAAAAA[C/T]TAGCTGGGCATGGTG	4799
rs541250881	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33292694	TGTCTAGTTGAACAT[A/G]TCCTGTATATGAGTA	4799
rs541272490	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33321280	AGGGATAAGAGGGTA[C/T]CTGCTATACCTCAGC	4799
rs541280296	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33305720	TCACCCAAAGTTTCA[G/T]GCTTTTGGAAATGGT	4799
rs541301930	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33300147	GCTCACTGCAACCTC[C/T]GCCCCCGGGTTCAAG	4799
rs541325292	snp	A/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33336722	CCTCCCACACAAGCC[A/T]CCCAAATAGCTGGGA	4799
rs541340514	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33299193	AATTAGCACTGGTAT[A/G]ATCATATTAACTAAA	4799
rs541356205	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33335364	GCCTCCTGAGTAGCT[A/G]GAATTACAGGCACCC	4799
rs541359579	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33336341	CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAC	4799
rs541371297	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33303752	TTTCTGTTTTTGAAT[A/T]TCTCAGTTCCCCCAA	4799
rs541398181	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33370403	CATTGCTTGCTTTAC[C/T]CAAACTGATCAAAAT	4799
rs541405100	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33349613	GCCTTTGGTCCTACG[A/G]GAGTAAAATTTCAGC	4799
rs541435265	snp	A/G	1.6571e-05	0.0028784	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33364063	ATCCTTTCAATATAC[A/G]TTCTTCAGGGTCAAA	4799
rs541489918	snp	A/C	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33356649	ACATTTTAAATCTAC[A/C]GTTGACCTGTACTGA	4799
rs541520146	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33304152	CTGTAATCCCAGCTA[C/G]TTGGGAGGCTGAGGC	4799
rs541564618	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33369823	TTCACAAATGGTAAA[C/T]CAGCTGATCCTTAAC	4799
rs541581129	in-del	-/AA			intron-variant	NFX1	GRCh38.p7	9:33333629	AAACCTGTAACTAGC[-/AA]AGTGAATGGAATTAC	4799
rs541617700	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33370469	ACCAAATAATGAATT[A/G]GTATACCATATCCGG	4799
rs541716591	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33290812	AGCTGGGTTTCGGAG[A/G]AGAGAGGACTTGTCC	4799
rs541716817	snp	C/G	0.0023933	0.0345097	intron-variant	NFX1	GRCh38.p7	9:33359430	ATGGTGAAACCCTGT[C/G]TCTACTAAAAATACA	4799
rs541732891	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33368299	GAGAATTGCCGGTGA[C/T]GGGGGTGGATAGTAC	4799
rs541802900	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33323198	AAGAGTGACACCAGC[A/G]GCTACATACTGTAGG	4799
rs541867996	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33336377	CCCGCCACCGCGCCC[A/G]GCTAATTTTTGTATT	4799
rs541897975	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33312646	GAGGCCGAGGTGGGT[A/G]GATCACTTGAGGTTA	4799
rs541936423	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33304133	TGGGCATAGTGTTGC[A/G]TGTCTGTAATCCCAG	4799
rs541939855	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33322405	AAGAAGATGGGGCTT[C/T]TTCTCCCCTCAGCTC	4799
rs542021749	snp	A/C	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33343962	GCACCCCCATAAATT[A/C]TCCTCTAAAAATACA	4799
rs542047834	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33298983	AGCAACTTAAAAGAA[C/T]GGAATTGGCATTTAC	4799
rs542059239	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33335503	CTCCCAAAGTGCTGG[A/G]ATTACAGTCATGAGC	4799
rs542061058	in-del	-/T	0.00279162	0.0372561	intron-variant	NFX1	GRCh38.p7	9:33358836	CAGCTAATTTTTACA[-/T]TTTTTTTGTACCACA	4799
rs542084395	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33306604	ATGAATTCCTCAAGG[A/G]CAAGGAGGAATCCTG	4799
rs542158578	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33315140	TGAGGCAGGAGAATC[A/G]CTTGAACCTGGGAGG	4799
rs542191080	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33356019	AGAAGTAGAATTGCT[C/G]ATTAATAGGGTTTAT	4799
rs542227996	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33345610	TGTTTGCATTTTTTC[C/T]CCAATGTAAAAGTGG	4799
rs542246324	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33325072	TGAGGAGGAGAGTAG[A/C]AAGAAGTGGAAAAAT	4799
rs542282543	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33346005	ACAGTTAGTCTGGCA[A/G]TATGATTCAGACTTA	4799
rs542286892	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33369151	GCTCACTGCAAGCTC[C/T]GCCTCCCGGGTTCAT	4799
rs542295537	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33309151	TCACGAGGCCAGGAG[A/G]TCGAGACCATCCTGG	4799
rs542300615	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33301809	AGGCATGATGGCTCA[C/T]GCCTGTAATCCCAGC	4799
rs542349814	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33300562	TGAGAGTATCTGGCT[A/G]TATTGAAATCTAGAA	4799
rs542373886	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33336292	GCTATCTCAGCTCAC[G/T]GCAAACTCCACCTCC	4799
rs542456303	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33298898	TGGAGACTTAGACTG[C/G]AGTAATAGTGTGGAA	4799
rs542486143	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33360566	TACACACAAACCTAA[C/G]AGAAAAAAATGCAAA	4799
rs542515224	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33326853	TATGTATAACAATAA[C/G]TGCACAAAAGGGGAG	4799
rs542648316	snp	A/C	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33293428	GAGTACCATTTTAAC[A/C]ATTTTGTGTGTGTTA	4799
rs542658268	snp	A/G	0.000518807	0.0160976	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352459	ATTGTGGACGGGGCA[A/G]TTCTTTCCTAGCATG	4799
rs542686904	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33300954	AGCAAGATCCTGTAT[C/T]GCCCAGTGGATCCTC	4799
rs542709750	snp	A/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33318509	TTAACAAGGCTTTTT[A/T]AATTTCTTCCTATGG	4799
rs542714944	snp	A/G	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33291642	GGCGTGGTGGCTCAC[A/G]CCTGTAATCCTAGCA	4799
rs542757260	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33299965	TAGTTTGACAAGTTT[A/G]AATTTTGACTTTTAA	4799
rs542801529	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33329590	AATTCTTCACTGTAC[A/G]TCTGTTTTGTCAGTT	4799
rs542907098	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33316212	TCTCTTCAAGAGAAT[A/G]AAGAGTTGCCTGTGC	4799
rs542962193	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33354990	ATTCACTCAGCACTG[C/T]GCTGCGTCTTTTACC	4799
rs542977674	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33331813	ATCAGATGTAGAAGC[C/T]GGGCAGCTAGCCAGA	4799
rs542980425	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33301943	CAGGCGTGGTGGCGG[A/G]CACCTGTAATCCCAG	4799
rs543035904	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352281	GAGGTTAAGCCTGGT[C/G]TAAAGGATCAAGTGT	4799
rs543043893	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33337464	TGGACTCCAAAAGTT[G/T]GTACACCCATCTACT	4799
rs543098339	snp	C/T	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33308415	CTATTGCACTCCAGC[C/T]TGGGCAACAAAGCAA	4799
rs543099388	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33316905	TTCTGACCCTTGATT[C/G]TTTTGCTCACAGCTT	4799
rs543144963	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33301519	GTTTAATTTCTCTTA[A/T]CTACTTTTTCTGCAG	4799
rs543181664	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33336840	GGCGCAGTAGCTCAC[A/G]CCTGTAATCCCAGCA	4799
rs543207898	snp	C/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33345945	TCATTTTACCAAATA[C/G]CAGAGGCAAACCTGA	4799
rs543257571	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33359294	TATTGTTGAATGGAG[C/G]GTGGTAATAATAGAT	4799
rs543302972	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33301795	TCTCATTTTTGGCCA[C/G]GCATGATGGCTCACG	4799
rs543383368	snp	A/G	0.000798403	0.0199641	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33364950	CATCTGTGGAAGCCT[A/G]TCCTGGTTCAGGACA	4799
rs543446482	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33291622	AGTTTAAAAAGTTAG[A/G]GCCGGGCGTGGTGGC	4799
rs543484997	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33290838	TGTCCCGGCGCTGCG[A/G]GTCGATGTGGGTGCC	4799
rs543485123	snp	A/C	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33298882	TTCAGGTAGGAGATG[A/C]TGGAGACTTAGACTG	4799
rs543486527	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33355266	GCAGATCAGTGAATC[A/G]TCACTAAATGATTAC	4799
rs543492777	snp	C/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33300253	TATTCTTAGTAGAGA[C/T]GGGGTTTCACCATGT	4799
rs543519508	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33298176	TTAAGAAGGTTAAGA[A/G]GACAGAGTGACAAGA	4799
rs543549348	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33358271	CTGGGACTGCAGGTG[C/G]CCACCACTACACCCG	4799
rs543569077	snp	A/C	0.0023933	0.0345097	intron-variant	NFX1	GRCh38.p7	9:33323764	TCTCAAAAAAAAAAA[A/C]AAACAAAAAAAAACA	4799
rs543571774	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33332064	GTCCCTGCATTAAAT[C/G]GTACAGATTGTCATC	4799
rs543592229	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33303616	CAGATTTGAGCAGTA[C/T]GAGTAAATAATAGTG	4799
rs543640035	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33362608	GTCTGACTGAGAAGA[A/G]GGACAGGGTGGAAAA	4799
rs543698319	snp	G/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33323437	AGATTTCACAAAGAC[G/T]GTAGGATAATCATAA	4799
rs543735289	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33330314	GCAGCATCTGACTTG[C/G]GAATAATTCTGAGGA	4799
rs543756739	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33329937	GTGCTGGGATTACAG[A/G]TGTGCACCACCACTC	4799
rs543768177	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33336815	ATTTTTAAAAGTTTT[C/T]CCAGGGCTGGGCGCA	4799
rs543806456	snp	A/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33343940	AAAACCTCTTTTGAA[A/T]AAAGTAGCACCCCCA	4799
rs543829478	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33333989	ATCTCTACTAAAAAT[A/G]CAAAAATTAGCCAAG	4799
rs543842294	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	NFX1	GRCh38.p7	9:33288810	TGCCTCCCCAACCCC[C/T]GCCTACCTACTGCTC	4799
rs543878040	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33295950	TATTTATTTGTTTTT[G/T]TGAGAGGAGTCTCAC	4799
rs544001032	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	NFX1	GRCh38.p7	9:33371519	TTTGCCGCTTGATGC[A/G]ATGAAAGTTTCACTG	4799
rs544002544	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33311622	CAGTGGTGCGATCTC[A/G]GCTCACTGCAACCTC	4799
rs544085813	snp	A/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33362041	TAGGAGGATGGCTTA[A/T]GCCCAGGAGGTGGAA	4799
rs544093866	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33319540	TTGGAGACAGAGTCT[C/T]GCTCTGTCGCCCCAG	4799
rs544165740	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33370495	TCCGGAATCACACAT[A/G]TTATCTTAAACCCAG	4799
rs544211067	snp	C/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33367169	TGCTGGACTCTGGTT[C/G]GAGGCATCCCCTGTG	4799
rs544271017	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33293769	TTCCACTTTGGGATT[A/G]TAGACCAGATTATAG	4799
rs544315830	snp	C/G			intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33351384	AGGATCACCTGAGCC[C/G]CAGGAAAGTCATAAT	4799
rs544393035	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33368235	GAGACAGACTCCATC[C/T]CAAAAAAAAAAGAAT	4799
rs544488688	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33327769	CCCCAGGTGATCCCC[A/G]TAGGGTCCTGGAAAC	4799
rs544552914	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33367842	TCTAGAGAGAGCAGT[C/G]ACTGGACATAATTTC	4799
rs544555881	snp	A/G	0.00199481	0.0315187	intron-variant	NFX1	GRCh38.p7	9:33310223	AATGTTTTACAGCAA[A/G]TTCTGTTACCCATCT	4799
rs544571279	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33326131	TTTGTATAAGAGGGG[A/G]GCTAGGCGCAGTGAC	4799
rs544605558	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33360125	AATTAGGAGTCCTAG[A/G]TATTCAGAAATGCTA	4799
rs544675872	snp	A/C	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33302595	TCCCAGGCTCAAGCA[A/C]TTCTGCATCAGCCTC	4799
rs544708297	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33325386	AACTGGCAACTGGCC[A/G]GGCGCGGTGGCTCAC	4799
rs544709509	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33322404	CAAGAAGATGGGGCT[G/T]CTTCTCCCCTCAGCT	4799
rs544783169	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33324293	CTAAGGCAGGAGAAT[C/T]GCTTGAACCCAGTAG	4799
rs544811217	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33354507	TTGGGCTGTTAAGAG[A/G]GGCACCTGTGGAGCA	4799
rs544842247	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33346868	CATGCTTGTCCTTCA[A/G]CACTTTAACATAAAG	4799
rs544885654	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33367777	TTAGGGTATCAGACA[C/T]GTTTGTTCCCACCAG	4799
rs544905662	snp	A/G	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33309284	ATGGCGTGAACCCGG[A/G]AGGCGGAGGTTGCAG	4799
rs544917920	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33297693	TGGCTGTTGGCCAGG[C/G]GTGTCTCTCTCAGCT	4799
rs544935196	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33333290	TTAGGAAGCTTCTGG[A/G]TGCAGGTAACAAAAC	4799
rs544937431	snp	C/T	0.000362343	0.0134551	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33318749	GCTATTGCGGCAGCA[C/T]CTCCCGAGATGTGTT	4799
rs544996003	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33338726	CAGTCAGAGAGCTCT[C/T]ATAGTCCCCATAACC	4799
rs545044085	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33346154	GTAGTTTGCAAGCCC[C/T]TCCTGTGGCATTCAT	4799
rs545050091	snp	C/T	0.0029563	0.0383329	intron-variant	NFX1	GRCh38.p7	9:33328557	TGCAGTTTTCATTTC[C/T]AGCTCTTTTCGTTTT	4799
rs545058781	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33294249	TAATGATTGATTAGT[C/T]CTCCACAAGCACCTT	4799
rs545113995	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33295489	ATTTTTAAATAAGTC[A/T]TATATTCACATAATT	4799
rs545145926	snp	A/G	9.88468e-05	0.00702948	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33318910	GTGTTTTCTTAACAG[A/G]GACTTGAAATGCGGT	4799
rs545158372	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33367453	GGCTGAGTTTCTAGC[G/T]TTCTGTCCATCTCCA	4799
rs545245927	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	NFX1	GRCh38.p7	9:33288669	TTTTTGTTGTTGTTT[C/T]AGATTTTCATGTGAA	4799
rs545320118	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33310062	TCTCCTATGGGTATT[A/G]TCTATCAAAATGAGT	4799
rs545321644	snp	A/C	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33309179	TGGCTAAGACGGTGC[A/C]ACCCTGTCTCTACTA	4799
rs545358790	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33317767	GATCACCTGAGCTCA[A/G]GAGTTCAAGACCAGC	4799
rs545420158	snp	G/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33366486	CCCTCCAGGCTTGCT[G/T]GGCAGTTAGTAAAAT	4799
rs545451713	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33369084	TTTTTCTTTTTTTTT[G/T]AGATGGAGTCTCGCT	4799
rs545471220	snp	C/T			intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33365964	GAGTTTAGTCAGAAG[C/T]CCCCAGCGCTGCATT	4799
rs545506717	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33306623	GGAGGAATCCTGTGC[C/T]TTCGTTTTACTCTTC	4799
rs545511053	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33338813	CAGTGGCATCTGGTA[A/G]CAACACAGAGGAAGA	4799
rs545517481	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33331982	CAAACCAAAGATCCT[G/T]CTTTATTTCACTTTG	4799
rs545550425	snp	C/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33331130	GAGATTGCACCACTG[C/T]GCTCCAGCCAGGGCA	4799
rs545597093	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33360052	CTTTCTAGTGAGTGC[C/T]GTTCAAAACCCTTGC	4799
rs545725911	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33307808	TCTTTTTTTTTTTTT[C/T]TTTTTTTGAGACAGG	4799
rs545740151	snp	G/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33325313	TCTCATCAGAAACAA[G/T]GGAGAACACATCACA	4799
rs545774838	snp	A/G	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33321492	AGTATAAGAGACTGG[A/G]TAGAGTTCTACTTTA	4799
rs545791851	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33369704	ATAAAATTCCCCATG[C/T]AATATGTAAATCTAG	4799
rs545811227	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33355181	TCCTGACTCAGAGAT[A/G]AGAGGTTTAAAACAA	4799
rs545811499	snp	A/G	0.00302877	0.038797	intron-variant, utr-variant-3-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33347787	CCAGCCCAACTGCCC[A/G]TCAGTCAACAAGTGG	4799
rs545914662	snp	C/T	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33335475	TGGCCTCATGTAATC[C/T]GCCTGCCTCAGCCTC	4799
rs545954315	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33328196	CTTGTTTTTGTGCTT[C/T]TTTTTTTTTTGGTAG	4799
rs545979899	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	NFX1, LOC105376018	GRCh38.p7	9:33348775	TTCTGCTACTGAGAA[A/G]GAAATACTCTACCAT	4799
rs546028557	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33306150	CAGTTAGAGAGGCAG[A/G]AACAGGAGAGCGATG	4799
rs546043440	snp	A/G	0.00119737	0.0244387	intron-variant, utr-variant-3-prime, downstream-variant-500B	NFX1, LOC105376018	GRCh38.p7	9:33348352	GCAAGACTCCGTCTC[A/G]AAAAAAAAAATAAAT	4799
rs546049984	snp	C/T	0	0	intron-variant	NFX1	GRCh38.p7	9:33334807	GACCCTTTTGGTGGT[C/T]ATTTAGGTTGTCTCC	4799
rs546114005	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	NFX1	GRCh38.p7	9:33289678	CCTGCCCTGCCCTGA[A/G]CTGCATGGTTCCCCT	4799
rs546126369	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33363606	GTATAAAAATGAAGT[A/G]TATATGTTAATGGAA	4799
rs546139191	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33322364	CAGCTCAGCTTGACA[C/G]ATCTCCACTCAGGAT	4799
rs546150048	in-del	-/C	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33337669	AGGAATTCGAGGTTA[-/C]AGTGAGCTATGTTAA	4799
rs546194751	snp	G/T	0	0	intron-variant	NFX1	GRCh38.p7	9:33345338	AAAACTTAGCCTGGC[G/T]TGGTGGTGGACGCCT	4799
rs546259872	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33343266	TTATCTTTATCTACC[A/G]TATTAGAAATTAAAA	4799
rs546266885	snp	A/G	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33320146	TTTTTTTGTATTTTT[A/G]TAGAGACGGGGTTTC	4799
rs546348847	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33342063	GGAGGTTGCAGTGAG[C/T]CAAGATCGCACCACC	4799
rs546360799	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33313885	TGATTGGTGTCAGAC[G/T]TTTAGTCACAAAGAC	4799
rs546373612	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	NFX1	GRCh38.p7	9:33290386	CTAGTCTCCTCCTCC[C/T]GCCCGACACCTGGCG	4799
rs546376893	snp	A/G/T	0.000296533	0.012173	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33319078	ATGCATGGACCCTGT[A/G/T]CCTTCATGTGGAAAA	4799
rs546435190	snp	A/G	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33304191	CGCTTGAACCTGGGA[A/G]GCAGAGGTTGCAATG	4799
rs546456813	snp	A/G	0.00318978	0.0398085	intron-variant, utr-variant-3-prime	NFX1	GRCh38.p7	9:33348005	CATGAGAATGATACA[A/G]TGGACTTTGGGGACT	4799
rs546490795	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33296702	GTACTCCAGCCTGGA[G/T]AACAGAGCAAGACCC	4799
rs546498748	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33370044	TATTTGCCAGCAGAT[A/G]AATCATGCCCGTTCC	4799
rs546522065	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33296413	CACTCAGTTCGCTGA[C/G]GAAGTCTTACTCATT	4799
rs546542983	snp	C/G/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33367959	TTACTCTGGGCCGGG[C/G/T]GCGGTGGCTCACGCC	4799
rs546585139	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33361138	TGTCGTATATAATAT[G/T]GAGAAACTGAGGAAC	4799
rs546623937	snp	G/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33361664	TGTAATCCCAGCTAC[G/T]CGGGAGGCTGAGGCA	4799
rs546654858	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33353161	CTTTGAAATTTCTCC[A/G]CTTCCTCCTTCCTCT	4799
rs546727665	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33360140	GTATTCAGAAATGCT[A/G]TAGTGAATACACAGA	4799
rs546756535	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33312785	TTGAGGTAGGAGAAT[C/T]GCTTGAAACCAGGAG	4799
rs546789290	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime, downstream-variant-500B	NFX1, LOC105376018	GRCh38.p7	9:33348480	ACACCACCTGTTCCC[C/T]AAGAACTATTGAAAT	4799
rs546817866	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33341097	TCTGCTGGTACCAGT[A/T]TACTGTATTAGTCTG	4799
rs546913253	in-del	-/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33347426	TCCCCTACTTCCAAC[-/T]TCTGAAAACCAATGT	4799
rs547022880	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33303549	CCATGTAGCAGAGAT[A/G]GGTGTGGACGTGGGC	4799
rs547058355	in-del	-/ATTATTATTATT			intron-variant	NFX1	GRCh38.p7	9:33363289	ATTATTATTATTATT[-/ATTATTATTATT]TTTAGACAGAGTCTC	4799
rs547107725	snp	C/T	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33309343	GCCTGGGCTACAGAG[C/T]AAGACTCCGTCTCAG	4799
rs547134631	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33357074	CCCAGCACTTTGGGA[C/G]GTTGAGGTGGGCAGA	4799
rs547136535	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33308972	GGCAGTCAGATACCT[C/T]ATTCCCTTTGACTGC	4799
rs547225010	snp	A/T	3.38249e-05	0.00411234	intron-variant	NFX1	GRCh38.p7	9:33347165	AGGCAGAGGTTCATG[A/T]TTTTATTACTTAAGA	4799
rs547226152	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33333088	TGACCTCAAGTGATC[C/T]ACCCGCCTCGGCCTC	4799
rs547226205	snp	A/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33339757	TGGGTATATACAGCC[A/T]TTCCAAATGGGAGAA	4799
rs547344876	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33291717	GACCATCCTGGCTAA[C/T]ACGGTGAAACCCCGT	4799
rs547356636	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33328309	GAATTATAGGCATGA[A/G]CCACCACACTTGGCC	4799
rs547360536	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33335617	TGCTTGGTCTCAAGT[C/G]ATCCTCCCATGTTGG	4799
rs547419659	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33331554	AGTCACTTTTGCTTT[A/T]TATCTGTAGAGAGCA	4799
rs547497959	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33306272	GACTCTGACAGAGTT[A/G]ACGTCACTGACAGAA	4799
rs547499965	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33297908	TTATATAGGGTATGC[A/G]TACCAGGGAGGTGGG	4799
rs547551978	snp	A/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33362985	CTGGGATTACAGGCG[A/T]GAGCCACCGTACCCA	4799
rs547582775	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	NFX1	GRCh38.p7	9:33289290	TTAGTTGGGGCGGGG[A/G]GCCCAGCTCCTGGGC	4799
rs547588302	snp	A/C	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33363795	AGTGTTCAGCCTATG[A/C]CTTGCTCAGATCCTT	4799
rs547590153	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33356371	TTCTGAATATGAGTC[C/T]TTTGTTGGCTCTATG	4799
rs547619471	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33329864	GGATTTTGCCATGTT[C/G]GCCAGGCTGGTCTCA	4799
rs547630471	snp	C/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33367927	TTAAGACTGAAACAT[C/T]GTGTAGTTAGGAATA	4799
rs547677987	snp	A/C	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33291152	AATTGTTCACTCACT[A/C]CCCCTCCTGGAGTTG	4799
rs547703974	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33304785	ATTCTTGAATATACT[A/T]CCAGAAAGGCAGCAT	4799
rs547720023	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33328986	CCAATTGAAAGTTCA[C/G]TGGTCCCTAAGACCA	4799
rs547760314	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33336489	AAAGTGCTGGGATTA[C/T]AGGCGTGAGCCACCG	4799
rs547763886	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33368680	AGAGGGGTGCCTACT[C/T]CTGTTCTGGCTTTCC	4799
rs547812979	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33320876	CTTTCAAGTGCCAGC[A/G]TGAATCAGTGGGAAC	4799
rs547839224	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	NFX1	GRCh38.p7	9:33289919	GTGAGATTGCACATT[C/T]AACTACTGTAAGGAG	4799
rs547876437	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33296815	CAGCCCTCACGCTTA[C/T]GTCTTTCTCTTAAAT	4799
rs547917042	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33341648	TTATAAAAAAATTTG[C/G]AGCCAGGCATTGTGG	4799
rs547920389	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33362821	CGATTCTCCTGCCCC[A/G]GCCTCCTGAGTAGCT	4799
rs548003003	snp	G/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33309306	AGGTTGCAGTGAGCC[G/T]AGATCATGCCACTGC	4799
rs548017001	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33355737	GCCACCTCTGCCTCC[C/T]GGGTTCAAGCGATTC	4799
rs548156556	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33341560	ATTTTTTAAATTTAT[A/G]TATTTAAGTGAAGAG	4799
rs548164580	snp	G/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33298381	GTGGTCAGAGAAATA[G/T]CAAGGGCTGGATCAT	4799
rs548299899	snp	A/C	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33313051	CTGAGTGTGTCAGAT[A/C]TGGGTACATGATAGC	4799
rs548330233	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33321581	GGGAAAACTATAAAA[A/G]AGCAACCATCAAGGC	4799
rs548334314	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33312363	GGGTTACTGTTAGCC[A/G]TGGTGCTAGGCAGAA	4799
rs548381092	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33336444	TGGTCTCGAACTCCT[C/G]ACCTCGTGATCCGCC	4799
rs548398625	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33334745	TGCATAACTCTTGTT[C/G]TTGCAGAGTATTCCA	4799
rs548416005	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33335923	ATGAATATACATTTT[A/G]TCCATTCACTGGTTG	4799
rs548417790	snp	C/T	0.00676609	0.0577691	intron-variant	NFX1	GRCh38.p7	9:33343372	TTTTTTAAATAACTT[C/T]TCAAAAAAGTAGAAT	4799
rs548544098	snp	A/G	0.00199481	0.0315187	intron-variant	NFX1	GRCh38.p7	9:33338059	GTCTCAGAAAAAAAA[A/G]AAGAAAGCAAAAAGG	4799
rs548616932	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33312222	TGAGATTACATGTAA[A/G]TGTTTTGACTCAGAA	4799
rs548641249	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33327450	GCTCACTGCAACCTC[C/T]GCCTCCCAGGTTCAA	4799
rs548641642	snp	A/C	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33296358	ACTTTTTTGTCTTTG[A/C]ATGGTGTTGCATGTG	4799
rs548642236	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	NFX1	GRCh38.p7	9:33289140	CTCCTGGCCTGCCAC[A/C]CCACCCCAGCGTTTA	4799
rs548675989	snp	A/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33303692	TTTTTATAAACCAGC[A/T]TTATAAACTCTATCC	4799
rs548684699	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33322894	AGTTCATCAGAGAGA[A/G]TCAGGGAAAGGTAGC	4799
rs548716566	snp	A/G	0.0023933	0.0345097	intron-variant	NFX1	GRCh38.p7	9:33345012	ACTAAAAATACAAAA[A/G]TTAGCCAGGCATTGT	4799
rs548736120	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33366246	TCACGATTTTTAAAG[C/T]AGAACATACTTTTAA	4799
rs548749224	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33350233	CGCTTGAACCCAGGA[G/T]GTGGAGGTTGCAGTG	4799
rs548766620	snp	A/G/T	9.89453e-05	0.00703306	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33366725	TATGGCCTGGAGAGC[A/G/T]TGAGCTATGACAGTG	4799
rs548770692	snp	A/G	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33359548	AGGGTGCAGTGAGCC[A/G]AGATGGCGCCACCAC	4799
rs548783803	snp	A/C	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33292787	TTTTCCTATCCTTTA[A/C]TAGGCTTCTCTAGAC	4799
rs548811336	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33313181	ATGCTGCTTCATGGA[A/G]CTCAGAGATGAAATC	4799
rs548888614	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33292138	GGGGCCTAGTTGTGA[G/T]TCTTCGTGTTGAACT	4799
rs548936492	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33331401	TAAAGCATGCTATAT[G/T]TAAGTCTTTATGGTA	4799
rs548996993	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33313843	GTTCTTTTCTGGAAC[C/T]TTATTAATGATTGTC	4799
rs549070034	snp	A/G			intron-variant, utr-variant-3-prime	NFX1	GRCh38.p7	9:33347983	CTAAGCTATGAGGAC[A/G]CAAAGGCATGAGAAT	4799
rs549080072	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33291955	CCTAGTCTTGATGTG[G/T]ATATTAAGTCTTCCT	4799
rs549152519	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33344290	GTCATGCTGTGATGG[C/G]TGCCCCTTGCTCCCG	4799
rs549211777	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33358831	CACACCCAGCTAATT[G/T]TTACATTTTTTTGTA	4799
rs549257048	snp	C/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33306890	TTATAGACGACTTGT[C/T]TTATAGGTATTTATC	4799
rs549272308	in-del	-/A	0.0103295	0.0711199	upstream-variant-2KB	NFX1	GRCh38.p7	9:33288828	CTACCTACTGCTCCC[-/A]GGGGTCTCTCCAGGG	4799
rs549324952	snp	C/G	0.000399281	0.0141238	missense, nc-transcript-variant	NFX1, LOC105376018	GRCh38.p7	9:33351576	TTCGGAGCAACATCC[C/G]CTGTCACCTGGTTGA	4799
rs549360887	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33370632	GCTTTACAGAATTCT[A/G]TTTCCTTAAGTCCCT	4799
rs549362556	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33363881	TGTTATTCTCTCCTT[A/G]ATAATCCAGTTTACC	4799
rs549418048	snp	A/C	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33343624	GTTTTTATTCTCTGT[A/C]ACAAAAATTTATTGG	4799
rs549439791	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33332104	TTCTTATATCTGCTT[C/T]TTATGGCTTTTTCTG	4799
rs549492145	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33296342	ATTCCCTGGATTCTA[C/T]ACTTTTTTGTCTTTG	4799
rs549511490	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33299390	TTTATTTACTTCTTA[C/T]TCAGGGAAGATTTTT	4799
rs549511874	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33350768	GACTAAGGCAAGAGG[C/T]TCACTTGAGCCCAGA	4799
rs549531919	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33350869	TTAAAAACTGAGCTG[A/G]GTGTGGTGGTTCATG	4799
rs549633150	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33306841	TCTCTCTGATCCTTC[C/T]AGCAGCAATTCGCAT	4799
rs549685939	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33371090	ATGAGCCCCAGAGCA[A/G]TAGCAGGAGACTTGA	4799
rs549691247	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33357892	ATTATAATATATACC[C/T]AAGAAACCTGCTGGG	4799
rs549730569	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33359324	TATTCCTTGGCCGGG[C/T]GCGGTGGCTCACGCC	4799
rs549730882	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33329723	GAGTGCAGAGGCGCA[A/G]TCTTGGCTCACTGCA	4799
rs549732508	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33321866	CTAGGCTGACAGAGT[A/G]AGACCCTGTCTCAAA	4799
rs549783872	snp	A/G	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33327115	CAGAAAACTAAAAAA[A/G]ACGAACATAAATCCA	4799
rs549848194	snp	A/C	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33337615	TACACCTGTAATCCC[A/C]ACATTTGGAAGGCCA	4799
rs549851409	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33291855	TTGCAGTGAGCCAAG[A/G]TCGTGCCACTGCACT	4799
rs549874074	snp	A/G	3.3012e-05	0.00406262	utr-variant-5-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33290566	GATCTAGGTTCTGCG[A/G]CACGGGATGGCGGAG	4799
rs549877671	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33291222	AACATCCATTTCCTC[A/G]GGGTGTTCCATAGAT	4799
rs549888202	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33299225	TACAGATGTTATTCA[C/G]ATTTCACCAGTTTTT	4799
rs549904358	snp	C/T			intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33353096	TCTAGTTCAAAGAAA[C/T]AGTGCTGCTTTATAT	4799
rs549913573	snp	A/G	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33336373	GGTGCCCGCCACCGC[A/G]CCCGGCTAATTTTTG	4799
rs549958351	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33310535	CATATCACTCAGCCC[A/G]GTTCTTTCCATGACC	4799
rs549969793	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33324095	AAAATTTTAAAAACT[C/T]AGGCCAGGCACAGTG	4799
rs550060554	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33315446	CCTGAAATATACTCT[C/G]TCCTTCGTCTGCCTT	4799
rs550063859	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33331571	ATCTGTAGAGAGCAT[A/G]TAGGGAACTTTTTCA	4799
rs550081145	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33364323	GGGGTAGGGTTGAGA[G/T]AAGAGTTTGGGTGGG	4799
rs550091038	snp	A/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33330547	CTGAGATGCTGTGAT[A/T]TGGCAATCATAAATT	4799
rs550114704	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33357746	AGACAGGGTTTTACT[A/G]TGTTGACCAGGGTGG	4799
rs550149376	snp	A/G	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33302739	CAGTGGCACGATCTC[A/G]GCTCACTGCAGCCTC	4799
rs550160769	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33369309	ACCTCGTGATCCGTC[C/T]GCCTTGGCCTCCCAA	4799
rs550161979	snp	C/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33325775	TAGCAGGCAGACTTG[C/T]CTTACAGTAAGTACT	4799
rs550188421	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33370270	AGAGTTGAGGGACTA[A/T]TGGGCTTTATTTGGA	4799
rs550206476	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33363024	TCTCGTGTTCTATGG[C/T]ACACTGGGGTGATGA	4799
rs550210364	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33361612	ACCCCATCTCTACTA[A/C]AGATACAAAAATTAG	4799
rs550262425	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33341476	TGTATATATATATAC[A/G]TAAACAAGGTAACAC	4799
rs550300615	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33306328	TTATAGAGGGAAGAT[A/G]TGAACTTTGACTGTG	4799
rs550313085	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33311421	AATGTGCCATGGATA[C/G]TACTTTTCTGTAACT	4799
rs550322722	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33357130	TCCTGGTAAAACCCC[A/G]TCTCTACTAAAAATA	4799
rs550439491	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33314207	CAGGCTGGTCTTGAA[C/G]TCCTGACCTCAAGTG	4799
rs550455057	snp	A/G	3.29641e-05	0.00405968	intron-variant	NFX1	GRCh38.p7	9:33303155	TGTAGCTTTTGGAAG[A/G]AAATTTATTTGGCCT	4799
rs550466801	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33344248	TCATTTAGGATCCTG[C/G]TGTGTTACTGTCTTC	4799
rs550486847	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33363836	TTATTTTCTTTTATG[A/G]AGACAATACCACCTC	4799
rs550517856	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33326378	AGATCATGCCACTGC[A/G]CTTCAGCCTGGGCAA	4799
rs550554592	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33333421	ATTTTGAAGACTTCA[A/G]TTTGGCTTCTCTGTG	4799
rs550560046	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33366830	GGCAAACTGGACCCA[A/G]GAAGCAGGGTCTGTC	4799
rs550575582	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33299309	TTAGTCATGTCTCCT[C/G]AGTCTCCTACCATCT	4799
rs550637146	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33360969	ATAACTTGAATGTTG[G/T]TGAGATGCCATGAGA	4799
rs550638489	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33303132	AGATTTAAATTTTTT[A/T]AATTACATGTAGCTT	4799
rs550653537	snp	C/T	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33308780	TTCTTACTTTTACTA[C/T]CCAAATCTAAGAGTA	4799
rs550700384	snp	A/G			intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352587	ATTTAAGAGTGAAAA[A/G]TGCTTTATTCACATA	4799
rs550723195	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33361533	ATCCCAGCACTTTGG[A/G]AGGTCGAGGCGGGTG	4799
rs550763929	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33354631	GGACCTCATCCAGCC[A/G]TTCCTGGATTGGGGT	4799
rs550832389	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33366181	TTCCTCTCCTAATTA[A/G]GAAACCCCAACAGAT	4799
rs550838978	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33293599	TTACCAATTTATAGT[A/G]TATTCTGTATGCTAC	4799
rs550873233	snp	G/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33338849	AGATAAGAGAAGGTC[G/T]CACACCCCAGAGCCC	4799
rs550931005	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33332909	AGAGTGCAGTGGCGC[A/G]ATCTCGGCTCACTGC	4799
rs550932916	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33325043	ACTGTATCAGTGTAC[A/G]TGTAATTGGAATATG	4799
rs551004114	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33301106	CTTTTTGGCCTCAGT[C/T]TGAATAGCCAGCTGC	4799
rs551005436	snp	C/T	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33291206	ATTTGTTCGTTGATA[C/T]AACATCCATTTCCTC	4799
rs551050646	snp	C/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33365199	GAATTCCTTGAACCC[C/G]GGAGGCAGAGGTTGC	4799
rs551075640	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33346424	ACCTTGAGGTTCTTA[A/G]CATTCTCCGAGAGGA	4799
rs551084670	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33317352	TGAGCCCGGGAGTTT[A/G]AGGCTGCAGTGAGCT	4799
rs551091405	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33358899	AGATGGCATCTCGCT[A/G]TGTTGGCCAGGCTGG	4799
rs551121521	snp	A/C	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33316413	ATGCACACCACCATG[A/C]CTGGCTTCAGCTGTT	4799
rs551123763	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33324797	AGCCAGGTGTGGTGG[C/T]GGGCACCTGTAGTCC	4799
rs551157898	snp	C/G	0.00358779	0.0422022	intron-variant	NFX1	GRCh38.p7	9:33291639	CCGGGCGTGGTGGCT[C/G]ACGCCTGTAATCCTA	4799
rs551168204	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33353237	GGGAAGATGTCCTGA[A/G]GTTAGGTGAATTGCT	4799
rs551169807	snp	C/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33338303	GATGTTGCAGTGAGC[C/T]GAGATCACACCACTG	4799
rs551184663	in-del	-/A	0.0023933	0.0345097	intron-variant	NFX1	GRCh38.p7	9:33334469	CTAAAACAATAAAAC[-/A]AAATAATAAAAACAT	4799
rs551196455	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33293491	GATATAGAGGTTGTT[A/G]CTATCTTCATTACAT	4799
rs551221793	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33322642	CACTCGTAGGGCAGA[G/T]GTTCCACTGAGAGAA	4799
rs551231623	snp	C/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33301923	CTAAAGATATAAAAA[C/T]TAGCCAGGCGTGGTG	4799
rs551232966	snp	C/T	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33338175	GTTTGGACAACATGG[C/T]GAAACCCTGCCTCTA	4799
rs551295573	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33325692	GAAAAAAAGAAAACT[C/G]TCAACCAAGAATCTT	4799
rs551305225	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33353044	CACTACACCTGGCTG[A/G]AAAGTTTCTTACATA	4799
rs551382141	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33318241	TTTATGTAAAACCTG[A/G]CATAAAGTATGAAAC	4799
rs551557896	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33302756	CTCACTGCAGCCTCC[A/G]CCTCCCAGGTTCAAG	4799
rs551562073	snp	C/T	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33360876	CTTGTGGGCACTAAG[C/T]TTGTAAGTGACTCTT	4799
rs551605053	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33301062	GAGTGTCTCCTTCCT[A/G]AATCCTCTTCCTCAG	4799
rs551623601	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33298622	ATCTCTGCAAAAGGC[A/G]AAAAAATAAAAATTA	4799
rs551648503	snp	A/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33366261	TAGAACATACTTTTA[A/T]AGGAAATAATATTTT	4799
rs551664465	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33345704	TCTGTCCCCTTGTAA[C/G]TATTTTTTTACAATA	4799
rs551681643	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33307949	GCTGGGACTACAGGC[A/G]TGTGCCACCACGCCT	4799
rs551688583	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33317466	AAAGAAATTGCACAT[A/G]CACTTACTGGAAGAT	4799
rs551716798	snp	A/C	0.00199481	0.0315187	intron-variant	NFX1	GRCh38.p7	9:33303880	TCCCTCTAGTTGTTG[A/C]TTTTTCAGATTTTGT	4799
rs551768146	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33317842	TTAGCTGGGCGTGGT[A/G]GCGGGCCCCTATAAT	4799
rs551770161	snp	C/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33361759	GCCTGGGCGACAAGA[C/G]CAGCCTGGGCGACAA	4799
rs551831606	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33323382	GAAACAGGGAAAAAA[A/G]CAGGCAACAGAAACT	4799
rs551833839	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33293915	AGTATTGTCATCCTT[C/T]ACCATAGACAAGGAA	4799
rs551848323	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33370665	CACTTCTCATACCAC[A/G]TCACTGAACCTGTTC	4799
rs551883580	snp	C/G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33323625	GGGCATGTTGGTATG[C/G/T]GCCTGTGGTCCCAGC	4799
rs551932825	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33337722	TGACAGAAAGAGACC[C/G]TGTCTCTTTAAAACA	4799
rs551969564	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33345086	AGAATTGTTTGAATC[C/T]GGGAGGCAGAGGTTG	4799
rs551980970	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33367969	CCGGGCGCGGTGGCT[C/G]ACGCCTGTAATCCCA	4799
rs551983244	snp	A/C	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33311626	GGTGCGATCTCGGCT[A/C]ACTGCAACCTCTGCT	4799
rs551984588	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352519	TTAGCTTCTTCCAGC[C/T]TGGAGAGTGGCCACC	4799
rs551997869	snp	A/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33292829	TCTTATTTCTGCCCC[A/T]CTTTCCAGTCTCGCT	4799
rs552002652	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33297491	GCTTATGATAACACA[C/T]ATTTACTATGCCACT	4799
rs552041195	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33296967	CCCTGCTGCCCCACA[C/T]AGCTCTTGAAACATA	4799
rs552112734	snp	C/T	0.0111196	0.0737302	intron-variant	NFX1	GRCh38.p7	9:33312116	GATCTTAAAATGATT[C/T]TTGAACCACAGGATG	4799
rs552172976	snp	A/G	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33354776	TTCCAGGTTGACTGA[A/G]ACTTCCTTTTCTTGC	4799
rs552189927	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33343319	GATTAGTATATTTAA[A/G]AATAATAATATACCT	4799
rs552251306	snp	A/G			intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33365922	GGCCAGGGATGTCAC[A/G]GAGGTAGCTTTAAGT	4799
rs552328354	snp	A/C	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33342443	CTCCAGCCTGGGCGA[A/C]AGAGCGAGACTCCAT	4799
rs552375121	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33366953	GCCAAAGAGCAAAAC[C/T]TATGCCTCGACCCAC	4799
rs552384663	snp	A/C	0.000399281	0.0141238	intron-variant, downstream-variant-500B	NFX1, LOC105376018	GRCh38.p7	9:33348981	ACAACATGCTATATT[A/C]TTTTATCTTCATGGA	4799
rs552509334	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33302501	CAAGCAGCTGAGACT[A/G]CAGGCACATGCCACC	4799
rs552519942	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33367234	ATAATGTGACCAGGA[A/G]GGGACAGGGAGGACC	4799
rs552550890	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime, downstream-variant-500B	NFX1, LOC105376018	GRCh38.p7	9:33348573	AAGTCTGAGATGTTG[C/T]GAGAATTACCAAAAT	4799
rs552581598	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33315180	CAGTGAGCTAAGATC[G/T]TGCCATTGCACTCCA	4799
rs552645083	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33309768	AAAGTGCTGAGAGTA[C/T]AGGCATGAGCCACCA	4799
rs552652103	snp	A/G	0.00318978	0.0398085	intron-variant	NFX1	GRCh38.p7	9:33295502	TCATATATTCACATA[A/G]TTTAGAAAGCAGAAA	4799
rs552662952	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33310513	GAGGGCTAATTCTGA[C/T]CTATAGCATATCACT	4799
rs552690971	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33302998	TTTTAATGAACCCCA[C/T]ATTTAGTGGAAAATG	4799
rs552705436	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33340817	CAAAATGTTGCCACT[C/G]TCTTTGATAAACAAC	4799
rs552770926	snp	A/C	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33340004	GTGTCTGTGGCTTTT[A/C]CAGGCACACAGTGCA	4799
rs552774862	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33327324	GCCACTGCACCCAGC[C/T]AAAAGCAGAAATTTT	4799
rs552805994	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33339473	ACCAGGTCCCTCCCA[C/T]AACATGTGGGAAGTC	4799
rs552808291	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	NFX1	GRCh38.p7	9:33289059	GCCCCCAGCCGGCCC[G/T]AGTGGGGGATATCGA	4799
rs552877245	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33340499	GGCTGCCATGAAGAC[C/T]TCTGATGTGCTCTGG	4799
rs552948206	snp	A/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33333708	CACTGGCTCCCAGTT[A/T]CTGAACAAAATTAAG	4799
rs553001162	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33338127	TGGGAGGCCATGGGA[A/G]GTGGATCACCTGAGA	4799
rs553069421	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33318642	GACTGTGCCAGGCCC[A/G]CATTTTGTATTTTCT	4799
rs553095694	snp	C/T	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33359942	TTTGACTTTCAGCAA[C/T]TTTAATAGTACCTCT	4799
rs553132532	snp	A/C	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33360580	AGAGAAAAAAATGCA[A/C]ATTTAAAGAAAAGTC	4799
rs553177851	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	NFX1	GRCh38.p7	9:33288555	GGCTGGGCAGGGCAG[A/G]GCAGGGCAGGGCCGG	4799
rs553211521	snp	A/C	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33300773	GTTAAGTGAATGACT[A/C]AAGACTTTGAGGGCA	4799
rs553214557	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33295719	TACGGGTGGTGTAGA[C/T]GTCTGGTTACAAGAT	4799
rs553248476	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33335635	CCTCCCATGTTGGCC[G/T]CCCAAAGTGCTGGGG	4799
rs553249146	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33308376	GAGTCCAGGAGTTCA[C/T]GGCTGCAGTGAGCTG	4799
rs553258479	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33344802	ACCCGGGAGGCAGAG[G/T]TTGCAGTAAGCTGAG	4799
rs553260588	snp	A/C	0.00199481	0.0315187	intron-variant	NFX1	GRCh38.p7	9:33317720	GTGGCTCACGCCTGT[A/C]GTCCCAGCCCTTTGG	4799
rs553303394	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33325224	AGTTAATGATAAGGA[A/G]AAAGTCTTGAAAGCA	4799
rs553310572	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33345845	GCTCAGATACCAGGC[C/T]AACAACCATTTGACA	4799
rs553375106	in-del	-/CA/CACACACACA	0.1655	0.246368	intron-variant	NFX1	GRCh38.p7	9:33342128	TCTGTCTCTCTCTCT[-/CA/CACACACACA]CACACACACACACAC	4799
rs553387606	snp	A/C	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33338315	AGCCGAGATCACACC[A/C]CTGCACTCCAGCCTG	4799
rs553388885	in-del	-/T			intron-variant	NFX1	GRCh38.p7	9:33316312	GTACTTACCAAGCCT[-/T]TTTTTTTTTTTTTGG	4799
rs553424155	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33337797	TTCACACCTGTAATC[C/T]CAGCACTTTGGGAGG	4799
rs553549966	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33339232	GACTAGGGAAGTTAC[A/C]AAAGAAAGAGGATTA	4799
rs553557310	snp	A/G	0.00279162	0.0372561	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33366429	ACTGTTGTGGCTCAC[A/G]GAGTAGGTGAAAGAA	4799
rs553644329	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33370213	TAGGTATGCAATCAC[A/G]CATTCAAAGAGGCTC	4799
rs553718119	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33354648	TCCTGGATTGGGGTC[C/G]CTGGGGAAATGGTAT	4799
rs553737040	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33302838	CCACGCCCAGCTAAT[A/T]TTTGCATTTTTAGTA	4799
rs553738386	snp	A/G/T			intron-variant	NFX1	GRCh38.p7	9:33345700	TTGATCTGTCCCCTT[A/G/T]TAAGTATTTTTTTAC	4799
rs553752052	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33332556	AAAGTGTCGTCACTC[G/T]GAATCTTGTTAGGGA	4799
rs553784800	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33336095	ATCTTGTGTTTAATT[G/T]TTTTGAAAAACTGCC	4799
rs553786742	snp	A/C	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33341989	GACATTGTTGTGGGC[A/C]CCTGTAATCCCAGCT	4799
rs553853700	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33297093	TCCGGAGCAGCATAG[C/T]AACTAGTCTGTCTTC	4799
rs553906346	snp	C/T	8.25362e-05	0.00642349	intron-variant	NFX1	GRCh38.p7	9:33313636	CTGATGCTGTCTTTA[C/T]ATCTATTGTCTTTAC	4799
rs553975337	snp	A/C	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33315594	GCTCAGAGACCACAC[A/C]TCCTCTTAAAAGTGG	4799
rs553995089	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33367749	GTACCATGTTCAAAT[A/G]TGTAATGTTTAGTTA	4799
rs554017577	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33326843	ATAGATGTGATATGT[A/G]TAACAATAACTGCAC	4799
rs554033751	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33296700	TTGTACTCCAGCCTG[A/G]ATAACAGAGCAAGAC	4799
rs554040735	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33361916	TCACTTGAGCTCAGG[A/G]GTTCAAGACCAGCCT	4799
rs554093222	in-del	-/GGGGCATTGTGGAC	0.00118959	0.0243594	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352439	GGTGGTTTCCAAAAG[-/GGGGCATTGTGGAC]GGGGCAATTCTTTCC	4799
rs554094756	snp	C/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33368031	TTAAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC	4799
rs554106665	snp	C/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33320086	CCTGCCTTGGCCTCC[C/T]GAGTAGCTGGGATTA	4799
rs554154574	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33329269	ATTGCCAACCAGGAA[A/G]GTTCACCCAGACCTG	4799
rs554222156	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33297069	TATCCTTTGGTTCAA[A/G]TTTTATCCTCCGGAG	4799
rs554236264	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33354996	TCAGCACTGCGCTGC[A/G]TCTTTTACCGTTATC	4799
rs554243027	snp	A/C	0.000399281	0.0141238	intron-variant, utr-variant-3-prime, downstream-variant-500B	NFX1, LOC105376018	GRCh38.p7	9:33348587	GCGAGAATTACCAAA[A/C]TGTGATGCAGACACG	4799
rs554247913	in-del	-/TT			intron-variant	NFX1	GRCh38.p7	9:33329489	GGCAAACAATGACAC[-/TT]ATATCAGGCATGGCA	4799
rs554255097	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33334600	TTTCAGATCTTTTTC[C/T]CTATTCATACAGATG	4799
rs554420424	in-del	-/A	0.0023933	0.0345097	intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33350006	GCAAGATTCTGCCTC[-/A]AAAAAAAACAAAACA	4799
rs554459979	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	NFX1	GRCh38.p7	9:33290271	TCAAGCCTGGGTAAG[A/G]CAGCAAGACCCTATA	4799
rs554499910	snp	A/C	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33312431	GTACTGCAAGCTGAT[A/C]ATTTATGTACATAAC	4799
rs554504160	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33303982	ATTCAGAAATTACCA[A/G]TGGGCCGGGCTTAGT	4799
rs554524783	in-del	-/CAAAACAAAA			intron-variant	NFX1	GRCh38.p7	9:33337751	CAAAACAAAACAAAA[-/CAAAACAAAA]ACTGATGGCCGGGCA	4799
rs554542814	snp	C/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33311707	ACAGGCGCCTGCCAC[C/T]GCACCTGGCTAGTTT	4799
rs554594699	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33339870	CTCCTTTGACTCCAT[C/G]TCTCACATCTAGGTA	4799
rs554599570	in-del	-/TACC	0.00478085	0.0486577	intron-variant	NFX1	GRCh38.p7	9:33305482	GGGCTGACCCTTTGA[-/TACC]AGTCTCAGATGTTGG	4799
rs554642426	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33296618	CACATGCCTGTAGTC[C/G]CAGACACTCAGGAAG	4799
rs554708360	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33304833	ATCAGTGGAAATTTG[C/G]GCAAATAGGACAATA	4799
rs554743835	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	NFX1	GRCh38.p7	9:33348284	TTGAACTCGGGAGGC[A/G]GATGTTGCAGTGAGC	4799
rs554807119	snp	C/T	0.000723047	0.019	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33354878	TGAGGAGTGTTCAGC[C/T]TTGGAAAGGAAAAAG	4799
rs554812829	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33333140	CATGAGTCACCACAC[C/T]GGCCTCGATTCCTGT	4799
rs554830058	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33367698	TTGTCCTGAGCTGCA[C/G]CAGCCATTGGTGGCC	4799
rs554831043	snp	A/C	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33303374	TTACTAATGAGACTT[A/C]AAAGCTCTAGGAGTC	4799
rs554868778	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33368011	GGCCAAGGCGGGTGG[A/G]TCACTTAAGGTCAGG	4799
rs554897926	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33335290	GGCTGGAGTGCAGTG[A/G]CGCAATCTCAGCTTA	4799
rs554989727	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33361251	AAAACAAAATAATAA[C/T]ATGAGAAATGCTAAC	4799
rs555080454	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33330617	GAAAATTGTAAGCAG[C/G]GTTGGGACATGTAAG	4799
rs555174191	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33317261	CCATCTCTACAAAAA[A/T]TACAAAAGCTAGCCA	4799
rs555202215	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33319822	GCCAAAGAACTAAAA[C/T]TGTAAGTACAATAGA	4799
rs555206029	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33311047	GACCCAGCTGGGACA[G/T]CTTTGTTCGGGTTTG	4799
rs555341204	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33319242	CAGAGGTTTCTAAAT[A/G]TTATGATCATATTTA	4799
rs555352837	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33323233	ATAGACTTCACTGAA[A/G]TAGTCTAGCCAAGTC	4799
rs555387465	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33319572	TCGAGTGCAGTGGTA[A/G]GATCTCAGCTCACTG	4799
rs555437916	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33313542	TGAGGGAAATGAAGT[C/T]AGAGAAAGGCTTAGT	4799
rs555480214	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33357244	GAGGCGGAGCTTGCA[A/G]TGAGCCGAGATGGTG	4799
rs555488919	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33330041	TCAGGTAATCTACCC[A/G]CCTCAGCCTCCCAAA	4799
rs555563791	snp	A/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33343812	TCCAGTCTAGAAATA[A/T]GTTGGGAAAAGTATT	4799
rs555600514	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33343078	AGATGGGGCCTAGTT[C/T]GTTAATAGATTCCTT	4799
rs555615308	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33322017	ACTAGCCTGGCCAAC[A/G]TGATGAAACCCCGTC	4799
rs555635868	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33291412	GTTTCGTTTAAAAAT[A/G]TGTCACAGCCCACTG	4799
rs555695671	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33316533	CTTGTTTCTGTTTAG[C/T]TGATTTTTCAAACCC	4799
rs555695817	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33307474	AGTTAACTTGTTGAA[C/T]CCTTACCACAGCCCA	4799
rs555697945	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33356571	CTATTTAGAAAAATT[G/T]GTCTATCCTGAGGCA	4799
rs555778212	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33298809	ATATTATTAAGCTGC[C/T]GTGTGGAGAATAGGC	4799
rs555786694	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33293634	AGTTCTGACTTTGCT[A/G]CTAATTTTATGTCCT	4799
rs555863474	snp	A/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33329940	CTGGGATTACAGGTG[A/T]GCACCACCACTCCTG	4799
rs555891649	snp	C/T	0.00318978	0.0398085	intron-variant	NFX1	GRCh38.p7	9:33369358	GTGAGCCACCACACC[C/T]GGCCATCCCATGCTA	4799
rs555913738	snp	C/T			intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33351412	AATCACACTGTTGCA[C/T]TCCAGCCTGGGCAAC	4799
rs555926791	snp	A/G	0.00199481	0.0315187	intron-variant	NFX1	GRCh38.p7	9:33363147	ATGGATATGCCTAAT[A/G]CACTGATTTGGTCAT	4799
rs555966467	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33297344	AGTTCTAGTTTCTTG[C/T]TTTATCAGGATTATT	4799
rs555990526	snp	A/C			upstream-variant-2KB	NFX1	GRCh38.p7	9:33290390	TCTCCTCCTCCCGCC[A/C]GACACCTGGCGCGTC	4799
rs556019675	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33364290	TTCTCGAAACTGTCC[C/T]CTTAAAGAACTGAAC	4799
rs556029775	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33326280	TAGTGTGGTGTGGTG[A/G]CATATGCCTGTGATC	4799
rs556081952	in-del	-/AG	0.00279162	0.0372561	intron-variant	NFX1	GRCh38.p7	9:33354280	TCAATCCTTCATAGT[-/AG]AGCCTTGCATACACA	4799
rs556089898	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33290800	GTGAAGCCCAGTAGC[C/T]GGGTTTCGGAGGAGA	4799
rs556167259	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33292653	TCTTATGGGTTTTTT[C/T]CCTGAGGGCTTTGCC	4799
rs556177336	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33336239	TTGTTTTTTTGAGAT[A/G]GAGTCCCACTCTGTT	4799
rs556228127	snp	A/C	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33354449	AGCTTAACCCATATG[A/C]GAATAGAGAACCCAG	4799
rs556254893	snp	A/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33319539	TTTGGAGACAGAGTC[A/T]CGCTCTGTCGCCCCA	4799
rs556282972	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33311828	AGTGTTGGGATTACA[A/G]GCATGAGCTACCGCG	4799
rs556283122	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33328347	GACTTAGGCAAATCG[C/T]CGTATACTTTAAAGC	4799
rs556288214	snp	A/C	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33357315	TCAAAAAATAATAAT[A/C]AATAAATAAAGTATA	4799
rs556294220	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33323490	CCAGGCATGGTGGCT[C/T]ACGCCTGTAATCCCA	4799
rs556306431	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33290717	TGCTAGGGCGTAGGA[C/T]AGTGGCTCGGAAGGG	4799
rs556312027	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33349444	GGTAGTAGAATGGGT[A/G]AGTGTTTAATGATTG	4799
rs556329349	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33315101	CGTGTTGGCGGGCGC[C/T]GGTAATCCCAGGTAC	4799
rs556357362	snp	A/C	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33315749	AAAAAAAAATTAGCC[A/C]GACATGGTGGCATGT	4799
rs556366681	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33368107	GGGTGTGGTGGCGGG[C/T]ACCTGTAAACACAGC	4799
rs556371683	snp	C/T			intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33350058	CCTGTAATCCCAACA[C/T]TTTGATAGGCTGAGG	4799
rs556439874	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33355980	TTGCTCTATATTTCT[A/G]TACATTTCTGTTGGA	4799
rs556475101	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B, nc-transcript-variant	NFX1, LOC105376018	GRCh38.p7	9:33348812	ATATAAACCACCAGA[C/T]GTGGTACACATTTTT	4799
rs556480704	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33362614	CTGAGAAGAGGGACA[A/G]GGTGGAAAAGGGAGG	4799
rs556501692	in-del	-/AAGTG	0.00636936	0.0560724	intron-variant	NFX1	GRCh38.p7	9:33341566	TAAATTTATATATTT[-/AAGTG]AAGAGTGATGAATTG	4799
rs556506479	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33342081	AGATCGCACCACCAC[A/G]CTCCAGCCTGGGCAA	4799
rs556558388	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33290684	GGCCTCAGCCACTCA[G/T]ATCGCGAGAGTAGCA	4799
rs556569768	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33305852	AATATGTCCAACAGG[C/T]AGGTAGCAATATTTG	4799
rs556621793	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33363860	CCACCTCATGTCCCA[A/C]GTTGTTGTTATTCTC	4799
rs556627308	snp	C/T	0.000148247	0.00860822	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33367541	TTTGTCCTCCTACCA[C/T]GCTGACAGGTGTGCT	4799
rs556641959	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33368759	CTGAAGGGTGGTTAC[A/G]GCAGTTCACAAGGTC	4799
rs556644922	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33341352	ATCATGAGAACAGCA[C/T]GGGAAAGACCTCCCC	4799
rs556652987	snp	C/T	0.0023933	0.0345097	intron-variant	NFX1	GRCh38.p7	9:33309139	AAGGCGGGTGGATCA[C/T]GAGGCCAGGAGATCG	4799
rs556676434	snp	C/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33325161	GAAACTCAGTAAACT[C/G]CAGGTAGGAAAGAGA	4799
rs556725128	snp	C/T	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33339420	CTATCACGAGAACAG[C/T]ACAAGAAAGACCTGC	4799
rs556744708	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33297951	CATCTTAGAATTCTA[C/T]TTAACAAATCTCTTG	4799
rs556746679	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	NFX1	GRCh38.p7	9:33290387	TAGTCTCCTCCTCCC[G/T]CCCGACACCTGGCGC	4799
rs556762179	snp	C/T	1.70778e-05	0.00292209	intron-variant	NFX1	GRCh38.p7	9:33338603	TGGTAAGTGGACTTA[C/T]TAGGCATAATCAGAT	4799
rs556819953	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33300927	GAGGATCCTGGAAAA[C/T]AGAAAATGCAAAGCA	4799
rs556842104	snp	C/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33304817	AAACTGGAAGTAAGA[C/G]ATCAGTGGAAATTTG	4799
rs556889006	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33292500	GGATTTAGGGTACCA[C/G]TTGTATTCTAGCCGT	4799
rs556921996	snp	A/G	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33308418	TTGCACTCCAGCCTG[A/G]GCAACAAAGCAAGAC	4799
rs556982079	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33313016	GCTGGGTCTCAGGAT[A/G]ATGCCATTGTGCTGT	4799
rs557060340	snp	A/T	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33298883	TCAGGTAGGAGATGA[A/T]GGAGACTTAGACTGG	4799
rs557120121	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33366413	ACCCTGTCCAGCTGC[A/G]ACTGTTGTGGCTCAC	4799
rs557146865	snp	A/G	3.30382e-05	0.00406423	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33294940	CTATGGTAGAGGACC[A/G]AAAGTCAAGGGGAAA	4799
rs557154609	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33333004	GTGTCCACCACTACA[C/G]CTGGCTGATTTTTGT	4799
rs557163928	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33299919	GAGAGCCAATATTAT[A/G]GAATATTACAGTGTG	4799
rs557173917	snp	A/G	0.00199481	0.0315187	intron-variant	NFX1	GRCh38.p7	9:33358131	TCTTGTATTACTTGT[A/G]ATTTTTTTTTTGAGA	4799
rs557200588	snp	C/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33307388	GGTTAGCATGTAATG[C/G]TTTGGGATGAAGGGT	4799
rs557217830	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33291000	TGGTGGCGTGGGCGC[C/G]AGCCGAATTCCAGTA	4799
rs557218036	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33334981	AACATTTTACCTCTC[G/T]TTTTCATCCATCCCT	4799
rs557262064	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33353294	ACAGCCAGGGCTAAG[C/T]TCTGTGCTCCTCTGG	4799
rs557312881	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33337384	AATATTATACCATTT[C/T]GTATAAGAGACTTCA	4799
rs557321733	snp	C/T	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33337774	AAACTGATGGCCGGG[C/T]ATGGTGGTTCACACC	4799
rs557340454	snp	A/G	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33324265	ACGCCTGTAATCCTG[A/G]CTATTTGGAAGGCTA	4799
rs557381723	snp	A/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33345152	GGGCAACAGAGTGAG[A/T]CTCCATCTCAAAAAA	4799
rs557425580	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33365428	AGCCTGGGCAACGTG[A/G]CAAAACCCTGTCTCT	4799
rs557489880	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33350463	AGATCATCTGCCCCT[A/G]CCAGTTAGTCATAGC	4799
rs557502296	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352935	AAGGTTTTTTTGTTT[C/G]TTTTGTTTTGTTTTA	4799
rs557505661	snp	C/G	3.98843e-05	0.00446549	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33332490	CTTCCATGTACCAGT[C/G]TCAAAAGTGAAGGTA	4799
rs557584836	snp	A/C	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33330876	AAAGTAAAAAAAAAA[A/C]TCTTCAAAAAGCTGA	4799
rs557587806	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33296859	TTACAGAACTTACAC[C/T]GGAAACCATAATTTA	4799
rs557655235	snp	A/G	0.000939392	0.0216521	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33313654	CTATTGTCTTTACAG[A/G]CACACAGTTCGCTGT	4799
rs557690033	snp	C/T	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33298880	TGTTCAGGTAGGAGA[C/T]GATGGAGACTTAGAC	4799
rs557821391	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	NFX1	GRCh38.p7	9:33371293	GTACAGCAGCAGGAA[C/T]AGGTGACTGGAGGGA	4799
rs557837965	in-del	-/A			intron-variant, downstream-variant-500B	NFX1, LOC105376018	GRCh38.p7	9:33348880	CAACTGTCCTATACC[-/A]AAAAAAAAAAGATAT	4799
rs557858209	snp	A/G/T	0.000102866	0.00717108	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33364766	ACCCTCGTGGAGGCC[A/G/T]TGAATAAGGTTGAAG	4799
rs557875732	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33339853	TAAAGCTACAAAATG[C/T]TCTCCTTTGACTCCA	4799
rs557910792	snp	A/C	0.00199481	0.0315187	intron-variant	NFX1	GRCh38.p7	9:33330781	GAAAAGCTATGTGTA[A/C]GTTGAATTTTTGCAA	4799
rs557947024	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33293201	CTGTGGCCTTGGGCA[A/G]GTTCCTACTCTCTGT	4799
rs557960916	snp	C/T	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33345349	TGGCGTGGTGGTGGA[C/T]GCCTGTAATCCCAGC	4799
rs558030610	snp	C/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33309088	CCTGGCTGGGCGCGG[C/T]GGCTCATGCCTGTAA	4799
rs558052472	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33299562	GTATAGTGGCACACG[C/T]TTGTGGTCCCAGCTA	4799
rs558081071	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33295827	TCTGCCTCATCTGGT[C/T]TGCTTAGTTGCAGCA	4799
rs558082609	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33300820	CACCACTCATGGGTT[C/G]TTGGAACCTGCCCAG	4799
rs558085693	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33337283	TTTTCTCATCATTTT[C/T]TAATAGCATTTACAT	4799
rs558125087	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33343875	ACTTCATATCTGTTC[A/G]TGCCTTTTTCACCAG	4799
rs558151198	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33292280	TTTAGTTCCCATTCC[A/G]TGTTCGTATTTTAGC	4799
rs558153948	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33350341	AAATAAAACGAAAAA[A/G]TGGCCCTGCCATCAG	4799
rs558188998	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33350975	CCAACATGGCGAAAC[C/G]CCAACTAAAAATACA	4799
rs558257484	snp	C/G	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33340110	TAGTAGGGACTCCGT[C/G]TGGGGGCTGCAACCC	4799
rs558258660	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33302725	CCCAGGCTGGAGTGC[A/G]GTGGCACGATCTCGG	4799
rs558280548	snp	C/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33356701	AGAGTTTACAATTCA[C/G]CTTTTTTCCACGTGA	4799
rs558310001	snp	G/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33327578	CACCATGTTGGTCAG[G/T]CTGGTCTCAAACTCC	4799
rs558356666	snp	A/C			intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33350570	TTTGGCTTCTGCTGC[A/C]AATCCTTTTGAGTCA	4799
rs558447902	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33291556	CAAGAAGACCATATA[C/T]GTATTTGTATACTGG	4799
rs558523111	snp	A/C	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33333935	GGATCACCTGAGGTC[A/C]GGAGTTCAAGGCCAG	4799
rs558559682	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33347542	ATAATAGATGTTGGC[A/G]TGGATGTGGTGAAAA	4799
rs558589402	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB	NFX1	GRCh38.p7	9:33288734	CCCCCTATGCGGGGT[A/G]TCATTTCACCATCCA	4799
rs558595523	snp	C/T	0.00318978	0.0398085	intron-variant, utr-variant-3-prime	NFX1	GRCh38.p7	9:33348076	CACACTGGGTCCGAG[C/T]ACGGTGGCTCATGCC	4799
rs558630289	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33355012	TCTTTTACCGTTATC[A/G]AAGAGCAAGAGAAAT	4799
rs558647485	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33310823	GCCAAGACTGTATTT[C/G]AAAATGTCATCTTTG	4799
rs558683242	snp	A/G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33353572	TTGAGTCACCTCATC[A/G/T]CTTCCCATGTAGCTG	4799
rs558720413	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33354394	GGAGACTTTTCCAGG[C/T]CTCACAGTAACCGAA	4799
rs558735727	snp	G/T	4.94752e-05	0.00497344	intron-variant	NFX1	GRCh38.p7	9:33338482	TCCTTTGTCTGGTTT[G/T]TTTTTTCTTTTTAAT	4799
rs558769771	snp	C/G	0.00279162	0.0372561	intron-variant	NFX1	GRCh38.p7	9:33341108	CAGTTTACTGTATTA[C/G]TCTGTTTTCACACTG	4799
rs558802017	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	NFX1	GRCh38.p7	9:33289359	GCCCCTGCCTGCCCC[C/T]CTCTGCCTTTTCCTC	4799
rs558856715	snp	A/G			utr-variant-3-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33370700	ACAATCAGTTTGGCC[A/G]TCCCCCATGATGGTA	4799
rs558888919	snp	A/G	4.94189e-05	0.00497062	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33318737	CTCTTCAAGTATGCT[A/G]TTGCGGCAGCACCTC	4799
rs558902080	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33333147	CACCACACCGGCCTC[A/G]ATTCCTGTTTTTATA	4799
rs558928469	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33339339	CATGGATAGCAGCAG[C/G]CAGAGAAAGAGAGTT	4799
rs559008668	snp	A/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33332690	AAATGCTGAAAAATA[A/T]AAGCTAAGTGCACTC	4799
rs559073871	snp	A/G	1.67548e-05	0.00289432	intron-variant	NFX1	GRCh38.p7	9:33319138	CTTAGGTAACTAGTA[A/G]GCGTAAAGTTGGCTT	4799
rs559097229	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33308125	ATGTCAGTCTTTTCC[C/G]TACAATAAATAGCCA	4799
rs559119675	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33333456	TCTTGATTTTCTCCT[C/T]GTGGGTATGTTAGCT	4799
rs559177632	snp	A/C	0.000128246	0.00800666	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352462	GTGGACGGGGCAATT[A/C]TTTCCTAGCATGTCA	4799
rs559179409	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33360556	CTTTCATAAATACAC[A/G]CAAACCTAAGAGAAA	4799
rs559220222	in-del	-/A	0.00119737	0.0244387	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33366232	TGTATCTGAATACTC[-/A]ACGATTTTTAAAGTA	4799
rs559260456	snp	A/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33294189	TTTTTACTCGACAAC[A/T]CTTAGCTGTCATTGG	4799
rs559304775	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33325613	AGCTTGCAGTGAGCC[A/G]AGATTGCGCCACTGC	4799
rs559315004	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33298383	GGTCAGAGAAATAGC[A/G]AGGGCTGGATCATGT	4799
rs559333088	snp	C/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33326101	AACAAATGAGGGAAG[C/T]CATAAGTGGTAAATT	4799
rs559389788	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33330651	GAAGTGGCTGCTGTC[A/G]GTTTTCTTCATTCTC	4799
rs559417937	in-del	-/T			intron-variant	NFX1	GRCh38.p7	9:33302089	ACAAACAAAAAAACA[-/T]TTTTTTTTCATTTTT	4799
rs559428620	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33353004	CACCTTGGCCTCCCA[A/G]AGTGCTGGGATCACA	4799
rs559470395	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33323898	TAGAAACTAGTTTTA[A/G]AAGAGGCCCAAATGG	4799
rs559483547	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33326234	CCTGACCAACATGGT[A/G]AAACTCCGTTTCTAC	4799
rs559494430	snp	A/T	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33308610	TTAAATAGTTATGTA[A/T]CCTTGGACAAGTTAT	4799
rs559507191	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33330994	CCATGGTGAAACCCC[A/G]TCTCTACTAAAAATA	4799
rs559533283	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33307780	AAGATGTCAATCTTT[G/T]TCTTTCTTTCTTTCT	4799
rs559668651	snp	A/G	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33316243	CCAGTTTGATTATCC[A/G]TTATGTCATATGGAT	4799
rs559702172	snp	C/T	0.00517822	0.0506191	intron-variant	NFX1	GRCh38.p7	9:33369429	ACTCTATTATGGAAA[C/T]GTTTTAGAGTAGAGA	4799
rs559725524	snp	A/G			missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33311168	AAACATGTGAATGTG[A/G]ACGAACCAGGTAAAG	4799
rs559785891	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33339619	GTCTTAACTCATTTC[A/G]GCATTAACGCAAAAG	4799
rs559817739	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33292578	AAATAAAAATGGTGC[C/T]TCTGATCTTTGCCAT	4799
rs559819303	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33360985	TGAGATGCCATGAGA[C/T]TCAGACACTGATGGC	4799
rs559844056	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33337465	GGACTCCAAAAGTTT[A/G]TACACCCATCTACTA	4799
rs559863450	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33314233	AAGTGATAATGCCTG[C/T]CTGGGCCTCCCAAAG	4799
rs559888372	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33295903	ACCTCTTAAACCAGC[A/T]TCAGAGAGCAATCTT	4799
rs559888390	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33305264	CAGCTGGATGATTAA[G/T]AGAAGCCTTCTTGGA	4799
rs559910071	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33317169	CACACCTGTAATCCC[A/G]GCACTTTAGGAGGCC	4799
rs559949421	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33324351	ACCACTGTACTCCAG[C/T]CTGGACGAGGGAGTA	4799
rs560039385	snp	A/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33324623	AACGATCAGTGAACA[A/T]GAAAATAGATTGAAA	4799
rs560069312	snp	A/G/T	0.00795532	0.062565	intron-variant	NFX1	GRCh38.p7	9:33299991	TTTAAATTTCTAGTT[A/G/T]TGTGACCTTGGATAA	4799
rs560071971	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33320505	TATATTCTTATCAGT[A/G]CTTTTAGTATGCTTG	4799
rs560074712	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33353861	GCCTGGCTAATTTTT[C/T]GTATTTTTAGTAGAG	4799
rs560142537	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33368294	GGGGTGAGAATTGCC[A/G]GTGACGGGGGTGGAT	4799
rs560205477	snp	A/G	9.94563e-05	0.00705112	intron-variant	NFX1	GRCh38.p7	9:33301460	TAGTTATTCTCCCCT[A/G]TTTGATACGTTTAAG	4799
rs560207628	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33328097	TTCACTGTAGCCTCA[A/G]CGTCCCATGCTCAGG	4799
rs560224856	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33298664	TGGCACATGCCTATA[A/G]TCCCAGCTACTCAAG	4799
rs560231383	snp	A/C	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33360765	TAGTGGCCAACTAAC[A/C]AAAACATCAAAAGAT	4799
rs560233348	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33321338	TAGGCTGAGTTGACT[G/T]AGAAGCTCAGAGACA	4799
rs560244238	snp	A/C	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33334736	ATGTCAGTATGCATA[A/C]CTCTTGTTCTTGCAG	4799
rs560347755	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33356134	GCTGTACATTTTTGT[C/T]AGCACTTGAAATTGT	4799
rs560436843	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33312047	ATACAAGGTCTCCTA[C/T]ATCATTAGTACAAGG	4799
rs560462267	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33362146	AAAAAAACAATTAGA[A/G]AAAAGGGAACACTTA	4799
rs560512970	snp	A/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33341322	AGCCATTAGATCTCA[A/T]GAGACTTATTCACTA	4799
rs560616685	snp	A/C	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33367435	CATAGTGCCAAAATC[A/C]AGGGCTGAGTTTCTA	4799
rs560617795	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33347187	TACTTAAGAATTGTT[A/G]GTCTCATCGTCTGTC	4799
rs560623375	snp	A/G	0.00199481	0.0315187	intron-variant, utr-variant-3-prime, downstream-variant-500B	NFX1, LOC105376018	GRCh38.p7	9:33348347	ACAGAGCAAGACTCC[A/G]TCTCGAAAAAAAAAA	4799
rs560642613	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	NFX1	GRCh38.p7	9:33288811	GCCTCCCCAACCCCC[A/G]CCTACCTACTGCTCC	4799
rs560690181	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33358600	TGTGCTTCAGCAGGC[A/G]TAAAAATATATCACA	4799
rs560696315	snp	C/T	0.00159617	0.0282053	upstream-variant-2KB	NFX1	GRCh38.p7	9:33289018	GGGTCTTGGCACTGT[C/T]TTCCTGGCCGGGGCC	4799
rs560744472	snp	A/G	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33326477	TAATCCCAGCTACTC[A/G]GGAGGCTGAGGTGGA	4799
rs560756424	snp	C/T	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33311436	GTACTTTTCTGTAAC[C/T]AGTAGTTCCCTGTGC	4799
rs560817061	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33355036	GAGAAATGCCGTTAC[C/T]AAGAATTGAATTGTC	4799
rs560850236	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33295984	TGCCCAGGCTAGAGT[A/G]CAGTGGTGCGATCCC	4799
rs560873428	snp	A/G	0.000328677	0.0128152	intron-variant, synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33347737	TGCACACGCATGTTT[A/G]TAGCAGCACAATTCA	4799
rs560882763	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33301531	TTAACTACTTTTTCT[A/G]CAGGGAGAGTATGTT	4799
rs560926221	snp	A/C	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33340196	GCAGCAAACTTCTGC[A/C]TGGACATCCAGGCAT	4799
rs560926673	snp	A/G/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33327118	AAAACTAAAAAAGAC[A/G/T]AACATAAATCCAGCT	4799
rs561000626	in-del	-/G	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33325638	ACTGCACTCCAGCCT[-/G]GGGCAACAGAGAGAG	4799
rs561026055	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33366208	AGATGTGTTTCTCTG[C/T]TTGTGTGTCTGTATC	4799
rs561075133	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33327927	CGACAGCATTCCACT[A/G]AAGTCATCCATGGCT	4799
rs561082067	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33360126	ATTAGGAGTCCTAGG[G/T]ATTCAGAAATGCTAT	4799
rs561097690	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33309286	GGCGTGAACCCGGGA[A/G]GCGGAGGTTGCAGTG	4799
rs561098342	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33333853	TTTGGTTATTAAAAA[C/T]ATAATTTGGGTCCAA	4799
rs561161676	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33360734	AGACAGGTTTTATTG[C/G]TGTTTAAATTTGAAT	4799
rs561183104	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33361539	GCACTTTGGGAGGTC[A/G]AGGCGGGTGGATCAC	4799
rs561185210	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33368246	CATCTCAAAAAAAAA[A/G]GAATAGTTACTCTGA	4799
rs561240147	snp	A/G	0.000159091	0.0089174	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294446	TTCAATACAGATGCT[A/G]CTGAATTCATTCCTC	4799
rs561244559	snp	C/T	0.000230597	0.0107352	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33318752	ATTGCGGCAGCACCT[C/T]CCGAGATGTGTTATG	4799
rs561275406	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33317899	GAGAATTGCATGAAC[C/G]GGGGAGGTGGAGGTT	4799
rs561299378	snp	A/C/G	6.80797e-05	0.00583403	intron-variant	NFX1	GRCh38.p7	9:33364127	TGTAACTTGTTACCT[A/C/G]CTTTCTTAATTGTGG	4799
rs561386439	snp	C/T	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33361468	TGAATATAATAATGG[C/T]GGTACTTAAAATTAT	4799
rs561413224	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33317358	CGGGAGTTTGAGGCT[A/G]CAGTGAGCTGTGTTC	4799
rs561415636	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33353100	GTTCAAAGAAACAGT[A/G]CTGCTTTATATACCT	4799
rs561456525	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33301939	TAGCCAGGCGTGGTG[G/T]CGGGCACCTGTAATC	4799
rs561463711	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33363713	CTCAGAGAAAGTCAT[C/T]CCCCATTGACCATTC	4799
rs561480716	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33325412	CTCACGCCTGTAATC[C/G]CAGCACTTTGAGAGG	4799
rs561533811	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33337400	GTATAAGAGACTTCA[A/G]TATCTGTGGATTTTG	4799
rs561536034	snp	A/T	0.0023933	0.0345097	intron-variant	NFX1	GRCh38.p7	9:33302798	CCTCAGCCTCCTGAG[A/T]AGCTGGGATTACAGG	4799
rs561638298	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33315213	CTGGGCAACAAGAGC[A/G]GAACTCTGTCTCAAA	4799
rs561686790	in-del	-/C	0.021333	0.101051	intron-variant	NFX1	GRCh38.p7	9:33345663	TAACTAGCTTTTTTT[-/C]CCCACTCTTATTATT	4799
rs561690582	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33291644	CGTGGTGGCTCACGC[C/T]TGTAATCCTAGCACT	4799
rs561743247	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33342232	TTTGGGAGGCCAAGG[C/T]GGGCGGATCATGAGG	4799
rs561779938	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33341586	AAGAGTGATGAATTG[G/T]GCAAGTATTATAAAC	4799
rs561828133	snp	A/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33357448	ATCTGGTAGTATATA[A/T]CCTCAACCATGACTT	4799
rs561832113	snp	A/G	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33299080	CAGATTTATAGAAAA[A/G]TTGCAAAGATAGTTC	4799
rs561864448	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33350584	CAAATCCTTTTGAGT[C/T]ATAACAGGGATTATT	4799
rs561900502	snp	A/C	0.000399281	0.0141238	intron-variant, downstream-variant-500B, nc-transcript-variant	NFX1, LOC105376018	GRCh38.p7	9:33348864	ACTGTTTGCTACATT[A/C]CAACTGTCCTATACC	4799
rs561915189	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33344559	ATATATATTTATCGT[A/G]TTAAAATTAAGAAAA	4799
rs561967631	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33336315	CCACCTCCCAGGTTC[A/G]AGTGATTCACCTGCC	4799
rs562002452	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33335511	GTGCTGGGATTACAG[C/T]CATGAGCCACCGTGC	4799
rs562009501	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33349848	ATCCTGTCTCTACAA[A/G]TAATACAAAAATTAG	4799
rs562019356	snp	A/T	0.00438332	0.0466095	upstream-variant-2KB	NFX1	GRCh38.p7	9:33289870	ACGCCCTCCCCACCC[A/T]GGGCCGAGCCCCCAC	4799
rs562034667	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33318221	GGGGACCTTTTTACA[A/G]GTGTTTTATGTAAAA	4799
rs562069969	snp	A/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33356022	AGTAGAATTGCTGAT[A/T]AATAGGGTTTATGTG	4799
rs562143206	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33321593	AAAAAGCAACCATCA[A/G]GGCTGGGCATGGTGG	4799
rs562202694	snp	A/G	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33355364	CCAGAACCGTCTCTT[A/G]TACTCTACATAAAGG	4799
rs562208895	in-del	-/G			intron-variant	NFX1	GRCh38.p7	9:33363618	AGTGTATATGTTAAT[-/G]GAATTCTTTACTTTT	4799
rs562238556	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime, downstream-variant-500B	NFX1, LOC105376018	GRCh38.p7	9:33348404	ACAATGTACACTCCT[C/T]GGGTGATGGGTGCAC	4799
rs562240198	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33320544	CTTTTAGTAATTCCC[C/G]CTTTCTTCTGATTTG	4799
rs562244370	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33304153	TGTAATCCCAGCTAC[C/T]TGGGAGGCTGAGGCA	4799
rs562257424	snp	A/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33369085	TTTTCTTTTTTTTTG[A/T]GATGGAGTCTCGCTC	4799
rs562279165	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33356551	TAATAAGCACTTTTC[A/G]TGTCCTATTTAGAAA	4799
rs562289252	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33321598	GCAACCATCAAGGCT[C/G]GGCATGGTGGCTCAT	4799
rs562300501	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33317027	GTTTCTTTACCAGTT[A/C]ATTGATTCTACAAAT	4799
rs562316036	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33322488	TACCCCTCCAACTCC[A/G]AGTTGAAGAGGCTGA	4799
rs562327629	snp	G/T	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33328918	CAGCCAACTAAGAAG[G/T]TAGAGGAAACACAGT	4799
rs562347166	snp	A/C	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33297526	CTGTGGGTCAGATGA[A/C]TGGGTCCTGGTTAGC	4799
rs562387513	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33290466	TCTGTGGCCGTCTAC[A/G]CGGCGCGCAGATGCG	4799
rs562481662	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33321565	AAAGCAAACAAAGCT[A/G]GGGAAAACTATAAAA	4799
rs562485201	snp	A/G	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33312820	AGGTTGCAGTGAGCC[A/G]AGATGGCTCCACTGC	4799
rs562504930	snp	A/C	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33355206	AAACAATGTTTAGTT[A/C]ACTTTTCGTTGAAGT	4799
rs562517362	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33301678	AATGATGGCTTTTAC[G/T]TATTATTTTTTCTTT	4799
rs562521372	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33320720	GGGTGTTGAAAGGCC[A/G]TGCATTTAGAAAAAA	4799
rs562547451	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33306153	TTAGAGAGGCAGGAA[C/G]AGGAGAGCGATGAGG	4799
rs562629914	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33363628	TTAATGGAATTCTTT[A/G]CTTTTCAGATTTCTA	4799
rs562636346	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33349751	ACTGCGTGAAGCTGT[A/G]GAGACCATGAGTTGG	4799
rs562666598	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33356787	CTCTGTCATACATCA[C/T]ATATAAGCCTGGGCA	4799
rs562796939	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	NFX1, LOC105376018	GRCh38.p7	9:33349038	GGGTGGTTCTCAAGT[C/T]CTTGGTATTTATTCT	4799
rs562850878	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33291319	TACACTTACATAAAT[A/G]TAAAAGCGAACCAGA	4799
rs562901942	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33303604	GCTTTGATAGTCCAG[A/G]TTTGAGCAGTATGAG	4799
rs562980334	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33344869	GACTCTGTCTCAAAA[A/G]AGAAAATAGAGGCCA	4799
rs563038013	snp	G/T	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33311287	AATAAATGGTAGGCA[G/T]GAATAGTACTTTTTT	4799
rs563040765	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33340584	AAATTTCTGCAGCCA[C/G]CTTGATTTTCTTCTC	4799
rs563063677	snp	A/G	0.00358779	0.0422022	intron-variant	NFX1	GRCh38.p7	9:33328217	TTTTTGGTAGACACA[A/G]GGTTTCACCATGTTC	4799
rs563109369	snp	A/G			intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352286	TAAGCCTGGTCTAAA[A/G]GATCAAGTGTGGCCA	4799
rs563143374	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33300284	TGGCCAGGATGGTCT[C/T]GATCTCCCGACCTCA	4799
rs563164978	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	NFX1	GRCh38.p7	9:33289795	CCTTCCCTGGCCGCC[C/T]ACTCACCCACACCTC	4799
rs563203078	snp	A/C	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33296703	TACTCCAGCCTGGAT[A/C]ACAGAGCAAGACCCT	4799
rs563203088	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	NFX1	GRCh38.p7	9:33289063	CCAGCCGGCCCGAGT[G/T]GGGGATATCGACACC	4799
rs563226447	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33358343	GTTAGCCAGGACAGT[C/T]TCAATCTCCTGACCT	4799
rs563236122	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33297645	AGGATTCAGTTCCTT[A/T]CAGATGTAGGACTGA	4799
rs563242274	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33292726	ATGCAGCCTTCTCTG[C/G]ATTCTCTAGTTGCAT	4799
rs563258642	snp	C/G/T	0.000292708	0.0120948	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352442	GGTTTCCAAAAGGGG[C/G/T]CATTGTGGACGGGGC	4799
rs563261235	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33300910	TGGATCTGATAGATT[C/T]AGAGGATCCTGGAAA	4799
rs563301839	in-del	-/T	0.458775	0.137524	intron-variant	NFX1	GRCh38.p7	9:33302968	CCACCACACCTGGCC[-/T]TTTTTTTTTTTTTTT	4799
rs563388344	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33304204	GAGGCAGAGGTTGCA[A/G]TGATCCAAGATCATG	4799
rs563399182	snp	A/G	0.0130921	0.0798413	intron-variant	NFX1	GRCh38.p7	9:33337964	TGAGGCAGGAGAATC[A/G]CTTGAACCTGGGAGG	4799
rs563432583	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33291635	AGGGCCGGGCGTGGT[A/G]GCTCACGCCTGTAAT	4799
rs563458701	snp	A/G	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33324822	TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG	4799
rs563461687	in-del	-/C	0.00318978	0.0398085	intron-variant	NFX1	GRCh38.p7	9:33359605	TCAGTCTCACCAAAA[-/C]AAAAAAAATAGATGT	4799
rs563471245	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33290881	AGGCTGTTTCTGGGG[C/T]AGCGGCGCACTGACC	4799
rs563525884	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33362943	TCCCAGCTTCAGGTG[A/T]TCCGCCCGCCTCGGC	4799
rs563559654	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33336827	TTTTCCAGGGCTGGG[C/T]GCAGTAGCTCACGCC	4799
rs563603922	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33293374	TCAATGCTCAAGCCT[G/T]TGTGTTTCAGATCCT	4799
rs563663170	in-del	-/AGACTGGATAGAGTTC	0.0685596	0.171987	intron-variant	NFX1	GRCh38.p7	9:33321485	CAGCTTCAGTATAAG[-/AGACTGGATAGAGTTC]TACTTTAAAGATGGT	4799
rs563681924	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33364875	AACCTAGAGTAGTTG[C/T]AGGAAAAAGTCACAA	4799
rs563708929	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33340660	TTCCAAACTTTTATG[C/T]TCTGTTTCCCTTTTA	4799
rs563735563	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33343944	CCTCTTTTGAAAAAA[A/G]TAGCACCCCCATAAA	4799
rs563850206	snp	A/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33310666	TTCACTAGCTGATAG[A/T]ATGTCTGTACTTCTT	4799
rs563857361	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33357781	AAACTTCTGGCTCAA[A/G]CGAACCTCCTGCCTT	4799
rs563952508	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33292058	CTGGATCTATTGATC[A/G]TCTCATCCACAGGCT	4799
rs564013625	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33364293	TCGAAACTGTCCCCT[G/T]AAAGAACTGAACTTG	4799
rs564022439	snp	A/G	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33364325	GGTAGGGTTGAGATA[A/G]GAGTTTGGGTGGGGT	4799
rs564035411	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33299197	AGCACTGGTATAATC[A/G]TATTAACTAAACTAC	4799
rs564035607	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33307570	ATCACAGTGGCAGGG[C/T]GTGGATGGTGGAGCT	4799
rs564037157	snp	A/G	0.00199481	0.0315187	intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33351256	TCCACTCAAGAGTTC[A/G]AGACCAGCCTGGGCA	4799
rs564155200	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33337520	ACCTTAAACACTACC[A/G]TTGCTATTTTTTTTA	4799
rs564213737	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33292704	AACATATCCTGTATA[C/T]GAGTACATGCAGCCT	4799
rs564240024	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33298134	ATATTTAATATGTCA[A/G]GTGGTGATAAGGACT	4799
rs564265931	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33331197	ATAAGCTGATAATTA[C/T]CACCTCATTGTTTAA	4799
rs564284182	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33290814	CTGGGTTTCGGAGGA[A/G]AGAGGACTTGTCCCG	4799
rs564297891	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33337918	GCCGGGCGTGGTGGC[A/G]CACACCTGTAATCCC	4799
rs564356538	snp	A/G	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33330287	GTTCTGTTAAACACA[A/G]TGCAGGGTCTGGCAG	4799
rs564374088	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33331774	CTGAGTACATGGCAA[C/T]CTGTAAATGACATCA	4799
rs564399409	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33300153	TGCAACCTCCGCCCC[C/T]GGGTTCAAGAGATTC	4799
rs564430731	snp	C/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33291729	TAACACGGTGAAACC[C/T]CGTCTCTACTAAAAA	4799
rs564442925	snp	A/G	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33317853	TGGTGGCGGGCCCCT[A/G]TAATCCCAGCTACTT	4799
rs564535970	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33345364	CGCCTGTAATCCCAG[C/T]TACTTGGGAGGCTGA	4799
rs564570776	snp	C/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33342440	GCACTCCAGCCTGGG[C/T]GACAGAGCGAGACTC	4799
rs564573246	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33370486	TATACCATATCCGGA[A/G]TCACACATGTTATCT	4799
rs564601328	snp	A/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	NFX1, LOC105376018	GRCh38.p7	9:33348945	ATTGGCCAACATTTC[A/T]TGAAACTCTTGACAT	4799
rs564603443	snp	C/T	0.000798403	0.0199641	utr-variant-5-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33290511	GCCGGAAGTCCGGGG[C/T]ACGTGACCTGGTGAC	4799
rs564665266	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33322055	AAAATACAAAAATTA[G/T]CCAGGCATGGTGGCA	4799
rs564679411	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33314165	ATTTTTGTGTTTTTA[G/T]TAGAGATAGGGTTTC	4799
rs564719300	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33319510	AAAATAATTGTGGGT[A/G]AGACAGAGTCTGGTT	4799
rs564751095	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33363808	TGACTTGCTCAGATC[C/G]TTATAGATCTGTTTA	4799
rs564764541	in-del	-/T			intron-variant	NFX1	GRCh38.p7	9:33358132	TTGTATTACTTGTAA[-/T]TTTTTTTTTTGAGAC	4799
rs564782043	in-del	-/T	0.0111196	0.0737302	intron-variant	NFX1	GRCh38.p7	9:33312114	AAGATCTTAAAATGA[-/T]TTTTGAACCACAGGA	4799
rs564790181	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33326295	GCATATGCCTGTGAT[C/T]CCAGCTACTCAGGAG	4799
rs564857007	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33328798	AGTGGTTGTGGCACT[C/G]AAGGTCCAGAGGCCT	4799
rs564883698	snp	A/G	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33360944	TGAAATCTAGCTTTA[A/G]AAAAATAAAATAACT	4799
rs564887022	snp	A/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33333324	AGAAAAAGTGACTTT[A/T]ACGATAAGGGTGTTT	4799
rs564912505	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33310523	TCTGACCTATAGCAT[A/G]TCACTCAGCCCAGTT	4799
rs564922982	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33339677	AAGGCAAGTCGCTTT[A/G]CCTATGAGCCTGTAA	4799
rs564991694	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33355356	GATAATTACCAGAAC[C/T]GTCTCTTGTACTCTA	4799
rs565008518	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33346812	ATCTGCTTCTGTTTT[C/G]GCATGTCTCTTCCTC	4799
rs565049278	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33367475	CCATCTCCACAAACA[A/G]TTCTCACTTTTCAAT	4799
rs565099130	snp	A/C	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33301870	TGAAGTCAGAAGTTC[A/C]AGATTAGCCTGGCCA	4799
rs565111570	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33339200	CATTTTCACACTGTC[A/T]GTAAAGACATACCCA	4799
rs565114565	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33306090	GGAGCAAAAAAGCAC[A/G]GAGGCAGGGAGGCTT	4799
rs565121557	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33303708	TTATAAACTCTATCC[C/T]GGCATCTTCCCTCTT	4799
rs565135572	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33367778	TAGGGTATCAGACAC[A/G]TTTGTTCCCACCAGA	4799
rs565140361	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33301087	CCTCAGCAAATTCCT[A/G]CCCCTTTTTGGCCTC	4799
rs565212980	in-del	-/G	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33342233	TTGGGAGGCCAAGGT[-/G]GGCGGATCATGAGGT	4799
rs565297634	snp	A/C	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33324723	ACGAGGTCAGGAGAT[A/C]GAGACCATCCTGGCT	4799
rs565331660	snp	C/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33332146	GTTTGGTGATGACTT[C/G]TCTTTCCTTTGCATG	4799
rs565334504	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33332023	GTGATATTATCAGGT[A/G]TGCTCTGAAGTGTGT	4799
rs565334516	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33323962	TGCAAAATTCATTAG[A/G]CTGGGTACCGTGGCT	4799
rs565366193	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33331455	AGTTCTGCCTTTCCT[C/G]ACAATTGTAGATAAC	4799
rs565443879	in-del	-/T	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33333199	AGCCATTTTAAAACC[-/T]TTTTGGAAAAGTGAT	4799
rs565477239	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33308671	ATAATGATAGTAATA[A/G]TAACACTTATAGGGT	4799
rs565529972	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33324251	GGGTGTGGCGGCACA[C/T]GCCTGTAATCCTGGC	4799
rs565550191	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33308353	AGGCTGAGCAAGGAG[G/T]ATCATTTGAGTCCAG	4799
rs565602033	snp	A/G	3.29538e-05	0.00405904	missense, nc-transcript-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352671	AGTGTGAATGTGGAC[A/G]AAGAAAAGAGATGGT	4799
rs565612962	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33365334	GTAAATGCCAGGCAC[A/G]GTGGCTCACACCTGT	4799
rs565645098	snp	A/G	0.000798403	0.0199641	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33366247	CACGATTTTTAAAGT[A/G]GAACATACTTTTAAA	4799
rs565729586	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33345087	GAATTGTTTGAATCC[A/G]GGAGGCAGAGGTTGC	4799
rs565770840	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33300221	AGCCACACTCCACCA[C/T]GCCCAGCTAATTTTT	4799
rs565835332	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33293456	TTATTAACTTGCTTT[A/C]CTCTTCACTGCAACT	4799
rs565958313	in-del	-/A			intron-variant	NFX1	GRCh38.p7	9:33334464	TATCTCTAAAACAAT[-/A]AAACAAAATAATAAA	4799
rs565979063	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33332210	AATTATTAGTCTACT[A/G]TGAATTTGGAGACCA	4799
rs565999171	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33322761	ACAAAAGAGAGCTCC[A/G]AGGTACTCTCCAAAG	4799
rs566084459	snp	A/G			missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33319067	AGTCGGAAAACATGC[A/G]TGGACCCTGTGCCTT	4799
rs566108869	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33303331	ACCTCAGTTCAGGAA[A/G]GGTGGTCTGCGGGGC	4799
rs566108971	snp	A/G	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33311576	TTTTTTTTTTGAGAC[A/G]GAGTCTCGGTCTGTC	4799
rs566114246	snp	C/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33292083	CAGGCTCGTTTCTGA[C/T]TCATTTCTGTACCCT	4799
rs566125925	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33357245	AGGCGGAGCTTGCAG[C/T]GAGCCGAGATGGTGC	4799
rs566141711	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33332089	GTCATCTGTTTTCAA[G/T]TCTTATATCTGCTTT	4799
rs566145226	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33310746	CTACAGGACCCTATT[A/G]GCCATTCTGCCTTTT	4799
rs566151738	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33299421	GTTTAATTTGGTTAA[A/G]TTTCTGTAATCCCAG	4799
rs566172616	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33370648	TTTCCTTAAGTCCCT[A/G]GCACTTCTCATACCA	4799
rs566183478	snp	A/G			upstream-variant-2KB	NFX1	GRCh38.p7	9:33290370	TATTTCCATCCAGCT[A/G]CTAGTCTCCTCCTCC	4799
rs566185288	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33363894	TTAATAATCCAGTTT[A/G]CCAAAATAGAGATAA	4799
rs566235673	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33300371	TCCAACCTGTTACAG[C/T]CTTTTTGAGAGGACT	4799
rs566263111	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33350930	GCAAGTGGATCACTT[C/G]AAGTCAGGAGTTCAA	4799
rs566355206	in-del	-/TA			intron-variant	NFX1	GRCh38.p7	9:33306937	CATTAGTCAAGATAG[-/TA]TTTTCGTAAGTAAAA	4799
rs566358539	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33358020	TCTTCTTTGATTTCT[C/T]TCAATGATACTTTAT	4799
rs566419069	snp	C/T			upstream-variant-2KB	NFX1	GRCh38.p7	9:33288485	CCTTCCCCAACAGGG[C/T]TATAGTTTCAGGGTG	4799
rs566423513	snp	A/G	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33344557	CAATATATATTTATC[A/G]TATTAAAATTAAGAA	4799
rs566425254	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33322663	ACTGAGAGAAGCAAG[C/T]CAAGAAGGCAAGAGG	4799
rs566469851	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33303816	TCATTCTTGCTGCTA[A/G]CCCATTTCTGCATGT	4799
rs566479220	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33347567	TGAAAAGGGAACACT[C/T]TTACACTGCTGGTGG	4799
rs566503159	snp	A/G	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33314006	TTTTTTCTTTTTGAG[A/G]TAAGTCTCACTCTGC	4799
rs566507775	snp	C/T	0.000798403	0.0199641	intron-variant, utr-variant-3-prime, downstream-variant-500B	NFX1, LOC105376018	GRCh38.p7	9:33348533	TCACTGATTGCAGGT[C/T]ACCCTAACAGATATA	4799
rs566516856	snp	C/G	0.000411824	0.0143437	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33319080	GCATGGACCCTGTGC[C/G]TTCATGTGGAAAAGT	4799
rs566535660	snp	C/T	6.59076e-05	0.00574016	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33367597	CCACCACCGATTCCT[C/T]ATCACAGACATCAGT	4799
rs566608110	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33360183	ATGGAAATGTACTTT[G/T]GGTGGTTGAAAGACA	4799
rs566622522	snp	G/T	0.000798403	0.0199641	upstream-variant-2KB	NFX1	GRCh38.p7	9:33289291	TAGTTGGGGCGGGGG[G/T]CCCAGCTCCTGGGCC	4799
rs566758783	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33354732	CTTCCTGGCCTGAGG[A/G]ATTGTTTTTTGGCAA	4799
rs566832610	snp	A/G	4.96134e-05	0.00498039	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294690	AATCGCCCAAGAGCC[A/G]TGGCCTTCAGAATCA	4799
rs566874608	snp	A/G	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33345847	TCAGATACCAGGCCA[A/G]CAACCATTTGACATC	4799
rs566883545	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33302124	TTTTACTATGCATAC[A/G]TAATAGTTTACATGT	4799
rs566905614	in-del	-/TT	0.00597247	0.0543191	intron-variant	NFX1	GRCh38.p7	9:33327560	TTAGTAGAGACAGGG[-/TT]TCACCATGTTGGTCA	4799
rs566909693	snp	G/T	1.64746e-05	0.00287002	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33319026	GCCAAACTCCTCTCA[G/T]CCAATTGCTAGAACT	4799
rs566930319	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33339804	GGGCTACAGGCCCCA[C/T]GCAAGTCCGAAATTC	4799
rs566967758	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33355521	TTGCATGTAGCAATG[C/T]TTTATTCATTTTTAT	4799
rs566983730	snp	G/T	0.00199481	0.0315187	intron-variant	NFX1	GRCh38.p7	9:33326036	ATAGATGGGATCAAA[G/T]TTGTGTTAGAATAAG	4799
rs567017785	snp	C/T	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33309351	TACAGAGCAAGACTC[C/T]GTCTCAGAGAAAAAA	4799
rs567020993	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33339779	ATGGGAGAAATTGGC[C/T]AAAACAAAGGGGCTA	4799
rs567078024	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33347456	TTGTCTGTTCCAATC[A/G]TTTTACTTTAAAATA	4799
rs567135911	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33333094	CAAGTGATCCACCCG[C/T]CTCGGCCTCCCAAAG	4799
rs567175786	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33339286	TGGGGAGGCCTCACA[A/G]TCATGGTGGAAGGCA	4799
rs567192953	snp	A/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33360452	TAGGTACTCAGTAAA[A/T]GTTATTGATTAAAAC	4799
rs567208900	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33292227	TTCTAGTCCAAAGAC[C/T]TCCTTACTCCTTTTC	4799
rs567267087	snp	A/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33310630	CACTGTTCCATTGTT[A/T]GCCCAGTGCCTGATT	4799
rs567268251	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33323074	ACTGAGCGTAATCCA[A/G]ATAAGGCACACAGTT	4799
rs567291860	snp	A/C	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33293004	TCCCCTAGAATTCTG[A/C]CTATGTGAAAGCTTT	4799
rs567293636	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33299328	CTCCTACCATCTCTG[A/G]CAGTTTCTTCATCTT	4799
rs567345370	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33354278	TCTCAATCCTTCATA[A/G]TAGAGCCTTGCATAC	4799
rs567347038	snp	C/T			intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33350266	CTGAGATGGCGCCAC[C/T]GCACTCCAGCCTGGG	4799
rs567373349	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33366861	AATACTTGTCTTTCT[C/T]ACTACCACTCTCCCT	4799
rs567410029	snp	A/G			intron-variant, utr-variant-3-prime	NFX1	GRCh38.p7	9:33348139	GTAGATTATGAGGTC[A/G]GGAGTTCGAAACCAG	4799
rs567410428	snp	C/T			synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33338541	TGACAAGCGGTGTAA[C/T]AAGAAACGGTTGTGT	4799
rs567426264	snp	C/T	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33295581	CCTAAGTTCTACCAC[C/T]ACTCGCTGCTCCCTG	4799
rs567441783	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33296220	GAGCCACTGCGCCCT[C/G]CCTAAAACACACATT	4799
rs567464198	snp	G/T	0.00119737	0.0244387	intron-variant, downstream-variant-500B, nc-transcript-variant	NFX1, LOC105376018	GRCh38.p7	9:33348871	GCTACATTCCAACTG[G/T]CCTATACCAAAAAAA	4799
rs567494221	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33302441	ATCATGTCTCACTGC[A/G]GCCTTGAATTCCTGG	4799
rs567569115	snp	A/G	0.000189602	0.00973474	intron-variant	NFX1	GRCh38.p7	9:33354204	TAATTTTTAAAATGC[A/G]TATATGTGCCTTCTT	4799
rs567603597	snp	A/G	1.65839e-05	0.00287953	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352741	GTTACTTAAATGTTA[A/G]CAACTGATGGCCTAG	4799
rs567620459	snp	C/G	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33301122	TGAATAGCCAGCTGC[C/G]TTACCCAGAATCAGA	4799
rs567635996	snp	G/T	0.00199481	0.0315187	intron-variant	NFX1	GRCh38.p7	9:33358915	TGTTGGCCAGGCTGG[G/T]CTCACATTCCTGGGC	4799
rs567670901	snp	A/G	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33351843	GTTCTGAGGCTACTA[A/G]TGAATCCAGAACTGT	4799
rs567699283	snp	A/G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33308005	AAATGGGGTTTTGCC[A/G/T]TGTTGCCCAGGTTGG	4799
rs567707776	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33302629	AAATGCTGGGATTAG[A/G]CACATGAGCCACCAT	4799
rs567721375	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33367368	AGGGGGTTAAATGCA[G/T]GTGGCCATGTCTGAG	4799
rs567747162	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33309346	TGGGCTACAGAGCAA[A/G]ACTCCGTCTCAGAGA	4799
rs567753032	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33325211	TAAAAATGCTAAAAG[C/T]TAATGATAAGGAGAA	4799
rs567765611	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33359467	AGCCGGGCATGGTGG[C/G]AGACGCCTGTAGTCC	4799
rs567779502	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33330814	AGAAGTCCTTAAATT[G/T]CAGGAGGAGCTCACT	4799
rs567799085	snp	C/T	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33362955	GTGATCCGCCCGCCT[C/T]GGCCTCCCAAAGTGC	4799
rs567844369	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33333038	TTTGGTAGAGACGGG[G/T]TTTCACTGTGTTGGC	4799
rs567861463	in-del	-/T	0.00199481	0.0315187	intron-variant	NFX1	GRCh38.p7	9:33335085	CAGTGGTTAGCCCAC[-/T]TTTTTTTTAGTTGAA	4799
rs567892282	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33338892	TGAGCACACAGTCTT[C/T]GGCAGAAGATTGTGT	4799
rs567930451	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33338304	ATGTTGCAGTGAGCC[A/G]AGATCACACCACTGC	4799
rs567934926	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33297714	TCTCTCAGCTCCTAG[A/G]GGCCACCTGTGTTTC	4799
rs568059563	snp	A/C	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33297076	TGGTTCAAGTTTTAT[A/C]CTCCGGAGCAGCATA	4799
rs568107627	in-del	-/A			intron-variant	NFX1	GRCh38.p7	9:33309362	ACTCCGTCTCAGAGA[-/A]AAAAAAAAAAAACTT	4799
rs568131090	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33355747	CCTCCCGGGTTCAAG[C/T]GATTCTCTTGCCTTA	4799
rs568158442	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33329840	ATTTTTGTATTTTTA[A/G]TAGAGACGGGATTTT	4799
rs568167483	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime, downstream-variant-500B	NFX1, LOC105376018	GRCh38.p7	9:33348633	GTTGGAAAAGTGGAA[C/G]AGATAGACTTGCTGG	4799
rs568174807	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33312823	TTGCAGTGAGCCGAG[A/C]TGGCTCCACTGCACT	4799
rs568196277	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33304586	CCTTCTTTTCTTTCA[A/G]TTCTTAACCACAGTA	4799
rs568223223	snp	A/T	0.0023933	0.0345097	intron-variant	NFX1	GRCh38.p7	9:33339911	AGGAAGTGGGTTCCC[A/T]TGGTCTTGGACAGCT	4799
rs568225742	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33358965	CAGCCTTCCAAAGTG[A/C]TGGGTTTACAGGCGT	4799
rs568268507	in-del	-/A	0.227959	0.249026	intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33350304	GCGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA	4799
rs568278951	snp	A/C	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33329230	TACTCTCTCCGCTTC[A/C]GTGTGTGCCAGCATA	4799
rs568294292	snp	C/T	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33336449	TCGAACTCCTGACCT[C/T]GTGATCCGCCTGCCT	4799
rs568341114	snp	C/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33291065	ACTCAGTCTCAGTCT[C/T]CTCATCTGTCAGTTG	4799
rs568360685	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33362455	AATGAAACCCTGTCA[C/T]TTGCAACAACATGGA	4799
rs568369548	snp	A/C	0.00199481	0.0315187	intron-variant	NFX1	GRCh38.p7	9:33342625	GGCTATTTTGAAGGT[A/C]TTTCCAGATATCATT	4799
rs568385335	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33368018	GCGGGTGGATCACTT[A/G]AGGTCAGGAGTTCGA	4799
rs568422184	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33368536	TTAGAGCACTTGGTC[A/G]TAGCCCCAGTTGTCC	4799
rs568423948	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33361825	CACATAGAGAGAAAC[A/G]TTATAGTGAAAAAAG	4799
rs568430850	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33333831	CATCTGTATCAAGGA[A/G]AAAAAGTTTGGTTAT	4799
rs568455077	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33347861	TCAGCCAGGAACGAA[A/G]TAATGGCATTCACAG	4799
rs568477107	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33334245	GGATCACTTAAAGCC[A/G]GGAGTTCAAGACCAG	4799
rs568482499	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33317879	TACTTGGGAGGCTGA[A/G]GCAAGAGAATTGCAT	4799
rs568492263	snp	A/C	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33296555	CAACATAAGGAGACC[A/C]TGTCACTACAAAAGA	4799
rs568562609	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	NFX1	GRCh38.p7	9:33289185	GCCCTGGTCACTTGG[C/T]AAGTGGCTGGGCCTG	4799
rs568580876	snp	A/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33320837	TTTGGTTTCCATTTC[A/T]TCAAAAGGAGAGAGT	4799
rs568617198	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33328303	GTGCTGGAATTATAG[G/T]CATGAGCCACCACAC	4799
rs568636250	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33313410	TCTGGGCAATATAGT[C/G]AGACCCTGTCTCTAT	4799
rs568656837	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33312370	TGTTAGCCATGGTGC[C/T]AGGCAGAATGGCAGC	4799
rs568695289	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33311697	AGCTGGGATTACAGG[C/T]GCCTGCCACCGCACC	4799
rs568710816	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33328430	CCAGATGAAGGGAAG[A/G]TAGGGAAGAAGCATT	4799
rs568713086	snp	A/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33355578	ATTCATTTACCCATT[A/T]TACTGTTAATGGATA	4799
rs568716771	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	NFX1	GRCh38.p7	9:33290141	ACATGGCGAAACCCG[C/T]CTCTACTAAAAATAG	4799
rs568777488	snp	C/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33312152	AATCATGCAGATTTT[C/T]GGTGAGGTGCGTTTG	4799
rs568819103	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33358440	ACTTTTAATTTTTTT[A/T]AAATTATTATTATTA	4799
rs568823615	snp	A/G	0.0023933	0.0345097	intron-variant, utr-variant-3-prime	NFX1	GRCh38.p7	9:33348171	CTGGCCAACAAGGTG[A/G]GACCCCCCCCATCTC	4799
rs568845169	in-del	-/T			utr-variant-3-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33370438	AGGAGCACAAATGAA[-/T]TTTTTAGTCTGAAAT	4799
rs568847390	in-del	-/CTCT	0.00119737	0.0244387	intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33349322	AGGAGGATGGAAGGG[-/CTCT]CCAGGTGTTCTGGAA	4799
rs568856171	snp	C/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33297022	AAAAGTTCATCCTTA[C/T]ATTGAACTGAAAGCT	4799
rs568911340	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33361770	AAGAGCAGCCTGGGC[A/G]ACAAGAGCAAGACTC	4799
rs568958378	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33335814	ATATTCTTTTGTGCC[C/T]TGCTTCTTTCACTTA	4799
rs568987827	snp	C/G	2.28757e-05	0.00338191	intron-variant	NFX1	GRCh38.p7	9:33354822	CAGTCTGTATTCTGA[C/G]TTTAATTTTTTTTCA	4799
rs568996955	in-del	-/T			upstream-variant-2KB	NFX1	GRCh38.p7	9:33288693	TGTGAAGGCAGAGAG[-/T]TTTTTTTTCTTTTTT	4799
rs568998474	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33346521	CAGCAACCCATCTGC[A/G]TAGGAACTGAGACAC	4799
rs569035202	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33347275	TATAATTTGCATACA[A/G]CAGAATTTACCCTTT	4799
rs569108978	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33342469	TCCATCTCAAAAAAT[A/G]TATATGTATGTATCA	4799
rs569145311	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33367972	GGCGCGGTGGCTCAC[A/G]CCTGTAATCCCAGCA	4799
rs569162050	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime, downstream-variant-500B	NFX1, LOC105376018	GRCh38.p7	9:33348574	AGTCTGAGATGTTGC[A/G]AGAATTACCAAAATG	4799
rs569227201	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33339370	TGTCCAGGAAATGGC[C/T]TTAGAAAGCCATCAG	4799
rs569278498	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33295522	GAAAGCAGAAAGTAT[A/G]GAAAGTTACACTGTA	4799
rs569402956	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33350820	ACATAGTGAGACCCT[G/T]TCTCTAAAAATTAAA	4799
rs569413974	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33334196	GCAGTGGCTCACATC[C/T]GTAATCCTTATGCTT	4799
rs569416990	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33303054	TTGTGAATTTGTTCC[C/T]TAAATGTCTGATATG	4799
rs569445819	snp	A/G			intron-variant, downstream-variant-500B	NFX1, LOC105376018	GRCh38.p7	9:33349157	ACAGATATCGAGTAT[A/G]AGTACCTACTATGTG	4799
rs569463922	snp	C/T	0.00279162	0.0372561	intron-variant	NFX1	GRCh38.p7	9:33319756	ACCAAGTGATCCACC[C/T]GCCTTGGGTTCCCAA	4799
rs569499613	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33327430	AGTGCAGTGGCATGA[C/T]CTTGGCTCACTGCAA	4799
rs569532365	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33326626	TCAAGAGGCTAAAGT[G/T]GGGGATCACTTGAGG	4799
rs569586912	snp	C/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33337089	ATTATGTTGGCCAGG[C/T]TGGTCTCAAATTCCT	4799
rs569617476	snp	C/T	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33364626	ATTGTCTATTGTCTA[C/T]GCTTTACAGGGAGAG	4799
rs569697662	snp	A/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33313449	AAAAACAAAAACAAA[A/T]ACAGAAGAAGAAAAA	4799
rs569706083	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33336654	TCACCTTGACTGGAG[G/T]GCAGTGGCAGACCAC	4799
rs569721993	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33310572	CCTTTCATTCTCTCC[A/G]TGTTACTCACTAGCA	4799
rs569789485	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33341797	TAGCCAGTTTCATAA[C/G]CCGGTCTCTAAATAA	4799
rs569798737	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33291353	TTCTGGAAGCAGTGA[A/G]GTTGGTTGGTTTGTT	4799
rs569829262	snp	C/T			missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33366702	TCATCCATGACTTGG[C/T]CCAAGTTTATGGCCT	4799
rs569885213	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33315750	AAAAAAAATTAGCCA[C/G]ACATGGTGGCATGTA	4799
rs569889381	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33324223	GTCTCTACTAAAAAT[A/G]TAAAAATTAGCTGGG	4799
rs569894298	snp	A/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33331338	GGTTGTTTTCATTTC[A/T]TCACTTTGGTGGGAT	4799
rs569927394	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33323689	ACCCAGGAGGCAGAG[A/G]TTGCAGTGAGCCGCG	4799
rs570013691	snp	A/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33329099	GGTTACAGTTTTATT[A/T]CAAGGAAAAGGATAC	4799
rs570108431	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33370063	CATGCCCGTTCCCCT[A/C]TGCCTGGCAGAATCA	4799
rs570120961	snp	A/T	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33298795	TCTCAAAAAAAAAAA[A/T]ATTATTAAGCTGCTG	4799
rs570177442	in-del	-/T	0.0158469	0.0875917	intron-variant	NFX1	GRCh38.p7	9:33353684	ATCTGATAGATTTGC[-/T]TTTTTTTTTTTTTTT	4799
rs570198079	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33357091	TTGAGGTGGGCAGAT[C/T]ACAAGGTCAGCAGAT	4799
rs570234433	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33363844	TTTTATGAAGACAAT[A/G]CCACCTCATGTCCCA	4799
rs570462839	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33298644	TAAAAATTAGCTGGA[C/T]GTGGTGGCACATGCC	4799
rs570503483	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33342927	ATACTTTGAGAGATT[C/G]ATTTACTTAGAATTG	4799
rs570541419	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33328339	CTTTTTTTGACTTAG[G/T]CAAATCGTCGTATAC	4799
rs570574882	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33337844	ACCTGAGGTCAGGTG[G/T]TCAAGACCAGCCTGG	4799
rs570578589	snp	C/T	0.00795532	0.062565	intron-variant	NFX1	GRCh38.p7	9:33335203	CTTACATTTTTTCTT[C/T]TTCTCTATTTTATCT	4799
rs570585991	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33340866	AGTTCCCAACAAATT[C/T]CTCATCTCTATCTGA	4799
rs570601312	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33297937	GGAATCTGGAAGACC[A/G]TCTTAGAATTCTATT	4799
rs570601348	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33306305	AGGAAACCCTGAAAA[A/G]GGAGGAGTTATAGAG	4799
rs570613416	snp	C/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33334436	ACTCTATCCTGGTGA[C/G]AGAGCGAGACCCTAT	4799
rs570635918	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33367955	ATAGTTACTCTGGGC[C/T]GGGCGCGGTGGCTCA	4799
rs570648058	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33323626	GGCATGTTGGTATGC[A/G]CCTGTGGTCCCAGCT	4799
rs570658670	snp	A/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33336535	GGGCTTTTTAAATCA[A/T]AGCCATCCTAGTGAA	4799
rs570689933	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33336993	TGTAATCCCAGCTAC[G/T]CGGGAGGCTGAGGCA	4799
rs570767095	snp	A/G			missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33364107	TTGAAAGAAGATGCC[A/G]GGTATGTAACTTGTT	4799
rs570818153	snp	A/C	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33320927	TCAATCTGACCTTAA[A/C]ATTGTGTATAGAGGA	4799
rs570860319	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33368751	CAAAACCTCTGAAGG[A/G]TGGTTACGGCAGTTC	4799
rs570894587	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	NFX1	GRCh38.p7	9:33289965	AAATGTGAACCATGA[A/G]AATATCGGTGATACT	4799
rs570898384	snp	C/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33325726	TCTCATGAAACTAAC[C/T]TTAGAAAATGAAGAT	4799
rs570953205	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33312669	TGAGGTTAAGAGTTC[A/G]AGACCAGGTGGGCCA	4799
rs570969332	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33363412	GCCTCAGCCTCCTAG[C/T]AGCTAGGATTACAGG	4799
rs570970557	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33313324	CCGGGCGTGGTGGCT[C/T]AAGCCTGTAATCCCA	4799
rs570975850	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33332320	ATAGGGATTAGGCTC[A/G]CTCCAGACATGGCAA	4799
rs571012633	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33331756	AAGTCATTTTTCTCA[C/T]TTCTGAGTACATGGC	4799
rs571013094	snp	A/G	0.00517822	0.0506191	intron-variant	NFX1	GRCh38.p7	9:33321750	TGGGTATGGCGGCAC[A/G]TGCCTGTGGTCCCAG	4799
rs571032866	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33305811	TAGAAATGTTGAGCT[A/G]GAGGAGTGAGCAGAA	4799
rs571060259	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33353288	ATTGACACAGCCAGG[G/T]CTAAGCTCTGTGCTC	4799
rs571148577	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33317603	TGGGAGGTCGAGGCC[A/G]CAGTAAGCTGTGTTC	4799
rs571192893	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33366312	TCATTTTTGGGGAAT[A/G]TCACCCACTCCCCAG	4799
rs571236873	snp	C/T	6.63603e-05	0.00575984	intron-variant	NFX1	GRCh38.p7	9:33313818	GGGCACACCAGCTAG[C/T]AATGCTTGTGTTCTT	4799
rs571252493	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33296347	CTGGATTCTACACTT[C/T]TTTGTCTTTGCATGG	4799
rs571265107	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33331747	GGACTTTTAAAGTCA[C/T]TTTTCTCATTTCTGA	4799
rs571364819	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33325037	CCTTTAACTGTATCA[G/T]TGTACATGTAATTGG	4799
rs571405792	snp	C/T	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33309123	AGCACTTTGGGAGGC[C/T]AAGGCGGGTGGATCA	4799
rs571425919	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33359579	ACTCTAGCCTAGACG[A/G]TACAGCAAGACTCAG	4799
rs571437420	snp	A/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33309539	TTGACTTGGGAACTT[A/T]CTTTTACTTTCAGGA	4799
rs571510119	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33292899	AATTTAACCATTCCA[A/G]CCTTTAAATTATCTT	4799
rs571545173	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33304309	AATCACCAATGACTC[C/T]TTTCCAGCCATATCT	4799
rs571592449	snp	C/T	0.00318978	0.0398085	intron-variant	NFX1	GRCh38.p7	9:33307955	ACTACAGGCGTGTGC[C/T]ACCACGCCTGGCTAA	4799
rs571618909	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33350989	CCCCAACTAAAAATA[C/T]AAAAATTAGCTGGTC	4799
rs571706080	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33364168	TGTTTGGTCTTTTGA[A/G]ATGTCATAACTAATA	4799
rs571717585	snp	A/G	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33358719	CCAGGCTGGAGTGCA[A/G]TGGCACAATTACAGC	4799
rs571745606	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33357471	CATGACTTTTCTTCA[A/G]TATTGTCTTTGATTA	4799
rs571774177	snp	A/C	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33330660	GCTGTCAGTTTTCTT[A/C]ATTCTCCCACAATCC	4799
rs571787362	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33337771	CAAAAACTGATGGCC[A/G]GGCATGGTGGTTCAC	4799
rs571824103	snp	G/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33345100	CCGGGAGGCAGAGGT[G/T]GCAGTGAGCCAAGAT	4799
rs571897563	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33357281	CACTCTAGCCTGGGC[A/G]ACAGTGGGAGACTCC	4799
rs571961069	in-del	-/A	0.00199481	0.0315187	intron-variant	NFX1	GRCh38.p7	9:33305137	GAAACAGAGGCGAAT[-/A]AAAACGGTTAACTTA	4799
rs572007498	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	NFX1	GRCh38.p7	9:33371266	TACCCAGTCTGCTTC[A/G]AAAGGGATCAGGTAC	4799
rs572019177	snp	A/C	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33359071	TTGACTTATTTAGCA[A/C]CCTCGCTAAATTCAC	4799
rs572096874	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33315276	TCTTAGTGCAATGCA[A/G]TTATCCCCTTTTTGC	4799
rs572097385	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33344693	CAACATGGTGAAACC[C/G]CGTCTCTACTAAAAA	4799
rs572119143	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33336007	AACATTTGTATACAA[C/G]TTTTTGTTCCAATAC	4799
rs572123783	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33292611	CCAGTTTCCTGATCA[A/G]TGTGTCCTGTTTCCC	4799
rs572148174	snp	A/C/T			intron-variant	NFX1	GRCh38.p7	9:33357158	ATACAAAAAATTAGC[A/C/T]GGGCATGGTGGCGGG	4799
rs572159167	snp	A/G	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33305134	TGAAGAAACAGAGGC[A/G]AATAAAACGGTTAAC	4799
rs572187798	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33301494	TATTAAGCCCAGCTT[C/T]AAAAATACAGTTTAA	4799
rs572206981	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33326757	TATATATATTTGTTA[C/T]CTTTTTCAGCTTCTT	4799
rs572252801	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352090	AATGTATAAATGTCT[C/T]TTGTGCAAGACATAG	4799
rs572284676	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33308241	GAGGCCAGGAGTTCT[A/G]GACCAGACTAGGCAA	4799
rs572322870	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33307523	CTCTGCTTTACAGAT[A/G]AGGCTCAGAAAGGCC	4799
rs572335726	snp	C/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33298062	GCACTGTTCTAGGTA[C/T]AGGGAATGCTGATGG	4799
rs572384734	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33336336	TTCACCTGCCTCAGC[C/T]TCCCGAGTAGCTGGG	4799
rs572418074	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33297417	CAGAGTTGTTACTGA[A/G]TCCTTAAGGCTGGTT	4799
rs572484977	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33329501	CACTTATATCAGGCA[C/T]GGCATTCCACTAGGC	4799
rs572612634	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33291418	TTTAAAAATATGTCA[C/G]AGCCCACTGCCTTCA	4799
rs572632231	in-del	-/ATTA	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33310240	TCTGTTACCCATCTG[-/ATTA]ATTAGTCTTGGCTCT	4799
rs572663637	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33326136	ATAAGAGGGGGGCTA[G/T]GCGCAGTGACTCACA	4799
rs572678276	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33343829	TTGGGAAAAGTATTG[A/G]GAAGTTGTCAGGGTC	4799
rs572699512	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33290808	CAGTAGCTGGGTTTC[A/G]GAGGAGAGAGGACTT	4799
rs572779356	snp	A/C	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33333252	AAAAGGTCTTACTGT[A/C]GTCAGAAAGAAAGCT	4799
rs572807363	in-del	-/T	0.000635664	0.0178165	intron-variant	NFX1	GRCh38.p7	9:33354908	GTAAGTAGTTGCAGC[-/T]GCTTTTTTAATCTCC	4799
rs572815955	snp	A/G			intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33350256	TTGCAGTGAGCTGAG[A/G]TGGCGCCACCGCACT	4799
rs572845025	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33346701	ATCTGAGCAGAAGTG[A/G]GCAGTTGCGGTTAAA	4799
rs572935120	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33341963	TCTACTAGAAATACA[A/G]AACTTACCTGGACAT	4799
rs573039091	snp	C/T	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33347499	TTAATAACCTCCTTA[C/T]TCCTGCAAGAATGGC	4799
rs573092223	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33295759	GTTGTGAAAACAAGT[G/T]GTGGGTGGTAACATC	4799
rs573195235	snp	A/G	0.000798403	0.0199641	intron-variant, downstream-variant-500B	NFX1, LOC105376018	GRCh38.p7	9:33349168	GTATGAGTACCTACT[A/G]TGTGCTAGGTAACAG	4799
rs573221212	in-del	-/AAAG	0.00557542	0.0525036	intron-variant	NFX1	GRCh38.p7	9:33345484	TCTGTCTCAAAAAAA[-/AAAG]AGAGATAAAGTCAAA	4799
rs573316234	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33338427	TATTGTATTCTTTGA[A/G]CCTATAGTTACTCAA	4799
rs573325622	snp	A/G	0.00318978	0.0398085	intron-variant	NFX1	GRCh38.p7	9:33309141	GGCGGGTGGATCACG[A/G]GGCCAGGAGATCGAG	4799
rs573351793	snp	C/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33337909	CAAAAATTAGCCGGG[C/T]GTGGTGGCGCACACC	4799
rs573363093	snp	G/T	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33297047	AAAGCTTCTTTCCTT[G/T]CCTTCCTATCCTTTG	4799
rs573364300	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33317698	GTCTTAATTATGGCC[A/G]GGCGTGGTGGCTCAC	4799
rs573392251	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33367072	CTGCCCATCATATCT[C/G]CTCTTTTCTCCTTCT	4799
rs573438931	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33323738	AGCCTGGGCAACAGA[A/G]CAAGACTTCATCTCA	4799
rs573452634	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33325312	TTCTCATCAGAAACA[A/G]TGGAGAACACATCAC	4799
rs573501651	snp	C/T			intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33351066	GGAGAATCACTTGAA[C/T]CCTGGAGGTGGAGGT	4799
rs573573696	snp	C/T			upstream-variant-2KB	NFX1	GRCh38.p7	9:33289605	TTCCCCCTTGCCCTG[C/T]CGTTCACCCTCCACC	4799
rs573579661	snp	A/G	5.14937e-05	0.00507388	intron-variant	NFX1	GRCh38.p7	9:33338611	GGACTTATTAGGCAT[A/G]ATCAGATTCCATTCA	4799
rs573581415	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33346004	CACAGTTAGTCTGGC[A/G]GTATGATTCAGACTT	4799
rs573688483	snp	G/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33359871	GTCTTTGAAATTTGT[G/T]TAAGATAAAAAGTTA	4799
rs573717023	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33300199	CTTGGATTACTACTG[A/G]GATTACAGCCACACT	4799
rs573750368	snp	G/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33366420	CCAGCTGCGACTGTT[G/T]TGGCTCACAGAGTAG	4799
rs573752828	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33316076	TGGTCTGTTCTCTGT[A/G]GAATAGAACTTCAAG	4799
rs573762705	snp	A/G/T	6.61141e-05	0.00574922	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294978	GTGAATGGAGTAACC[A/G/T]AACAACTCCAAAACC	4799
rs573797028	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33332869	TTTTCCTTTTGAGAC[A/G]GAGTCTCGCTCTGTT	4799
rs573846690	snp	C/T			intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33349670	GGAAACAGGCCATTT[C/T]TCAAGAAAAAAAAAA	4799
rs573875376	snp	C/T	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33333097	GTGATCCACCCGCCT[C/T]GGCCTCCCAAAGTGT	4799
rs573895458	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33341524	AGTACGTGTGTATGT[A/C]TGTATATAGCATACA	4799
rs573895665	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33317087	TTTATCAAATCAGTC[C/T]TTATTAAATGAACAA	4799
rs573911983	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33326285	TGGTGTGGTGGCATA[A/T]GCCTGTGATCCCAGC	4799
rs573965574	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33323856	TGAAGATGATGTCTT[A/G]TCAAATAGAGAATAT	4799
rs573999376	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33296254	CTGTGTCACTCCTCT[A/G]CTTAATTCCGTTTAC	4799
rs574067555	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	NFX1	GRCh38.p7	9:33290319	GAAAACCACAATGAT[C/T]ACGCAAGTCGCCGCC	4799
rs574104609	snp	A/G	0.0107246	0.0724382	upstream-variant-2KB	NFX1	GRCh38.p7	9:33289528	GGCAGGGGGTGCAGG[A/G]GAGGAAACTCCTCAC	4799
rs574124649	snp	A/C/T	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33299935	GAATATTACAGTGTG[A/C/T]GCTTTTGAGTCAGAT	4799
rs574164570	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33344458	CAAGAACTTTTCTTT[C/G]TTTGTGGTCTCCACT	4799
rs574201450	snp	A/C	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33343950	TTGAAAAAAGTAGCA[A/C]CCCCATAAATTCTCC	4799
rs574220205	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33360637	CACACATATATACAC[A/G]CATACACCTGTGTGT	4799
rs574241013	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	NFX1	GRCh38.p7	9:33288982	TCTGCTTGTTGTGGG[A/G]GTCAGTGCCACGGTC	4799
rs574243535	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33331792	GTAAATGACATCAAA[G/T]CCAAAATCAGATGTA	4799
rs574260229	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33330894	TTCAAAAAGCTGATA[A/G]TTGGCTGGGTGTGGT	4799
rs574317488	snp	A/G	0.00159617	0.0282053	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33365636	AGAAAGAAAAAGAAA[A/G]TAAAGATGCTGGCCA	4799
rs574353039	snp	C/G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33336017	TACAAGTTTTTGTTC[C/G/T]AATACCTATTTTCAT	4799
rs574395931	snp	G/T	0.00914312	0.0669923	intron-variant	NFX1	GRCh38.p7	9:33337778	TGATGGCCGGGCATG[G/T]TGGTTCACACCTGTA	4799
rs574431588	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime, downstream-variant-500B	NFX1, LOC105376018	GRCh38.p7	9:33348306	GCAGTGAGCCAATAT[C/T]GCACCACTGCACTCC	4799
rs574486594	snp	A/G	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33367300	TTGCCAGTGAAGAAA[A/G]CAAGTCTGACATGAA	4799
rs574494449	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33296642	CAGGAAGCTGAAGTG[A/G]GAGGATCACTTGAGC	4799
rs574525226	snp	A/C	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33360704	TAAAAACCTAGCAGG[A/C]CAAATTCAGCCCACA	4799
rs574525400	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33367707	GCTGCACCAGCCATT[G/T]GTGGCCTCCTCAGGC	4799
rs574526861	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33315525	TATTCTTTCCCCAGC[A/G]TTTCCTTTCAGGCCT	4799
rs574564266	snp	G/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33341203	CCAAGTGGCTGGGGA[G/T]GCCTCACAATCATGG	4799
rs574571432	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33322046	TCTCTACTAAAAATA[C/T]AAAAATTAGCCAGGC	4799
rs574574097	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33321131	TAATGACCAGAAATC[C/G]TACCCTGGCACTCAT	4799
rs574618461	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33318259	TAAAGTATGAAACCT[A/G]TGCTTCTTGGGTTGA	4799
rs574680129	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33328021	TCTGTGTTTTTGTTA[C/T]TTGTTTTGAAACAGG	4799
rs574685186	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33368886	GTCCCCAGGACCAGC[C/T]CCTCTCCACTCCTGG	4799
rs574714918	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33338402	TACATTATTACAATT[G/T]TATTATTACTATTGT	4799
rs574720492	in-del	-/CT	0.0115144	0.0749975	intron-variant	NFX1	GRCh38.p7	9:33325655	GGCAACAGAGAGAGA[-/CT]CTGTCTCAAAAAAAG	4799
rs574775093	snp	A/C	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33326793	GATATAACATTATAT[A/C]AAGTTCTAACAAAGT	4799
rs574828099	snp	G/T			intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33350966	GCCATCTGGCCAACA[G/T]GGCGAAACCCCAACT	4799
rs574846473	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33326194	AAGGTGGGCAGATCA[C/T]TTGATGTCAGGAGTT	4799
rs574874577	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	NFX1	GRCh38.p7	9:33288760	ATCCACATCCTTGTT[C/T]GCGTTTCTGGCCCTC	4799
rs574911273	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33295859	TTCCTAACTGGTCTT[A/G]TCATCTCTTAATTTC	4799
rs574964222	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33296052	CTGCATCAGCCTCCC[A/G]AGTAGCTGGGATTAC	4799
rs574999177	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33303449	GCCTTTGTGCTCCTG[A/G]CAAGCTGTTCTGGAG	4799
rs575001223	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33361724	GTTGCAGTGAACCGA[C/G]ATCATGCTATTGTAC	4799
rs575018320	snp	C/T	3.36106e-05	0.00409929	intron-variant	NFX1	GRCh38.p7	9:33342729	TTTTATGAACAAATA[C/T]AAATCTCTTTTCCCA	4799
rs575022931	snp	A/G	0.000399281	0.0141238	intron-variant, missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33347717	CATTATATGAAAAAG[A/G]TACCTGCACACGCAT	4799
rs575086498	snp	G/T	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33354551	AGCCAGGGAACACTC[G/T]GAGGCCACTGGAGGA	4799
rs575096048	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33320175	TCACCATGTTGGCCA[A/G]GCTGGTCTTGAACTC	4799
rs575146027	snp	A/G	3.31768e-05	0.00407275	intron-variant	NFX1	GRCh38.p7	9:33311066	TGTTCGGGTTTGGAT[A/G]CATGGCTGTGGTTTA	4799
rs575191635	snp	C/G	0.00358779	0.0422022	upstream-variant-2KB	NFX1	GRCh38.p7	9:33289440	CTTGTTTCAGGGACC[C/G]CAGGAGGTGGTGCCC	4799
rs575242952	snp	A/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33340127	GGGGGCTGCAACCCC[A/T]CATTTCCCTTCTGTA	4799
rs575323097	in-del	-/AT	0.00279162	0.0372561	intron-variant	NFX1	GRCh38.p7	9:33341409	GGTCCTTCCTACAAC[-/AT]GTGGGAATTCAAGAT	4799
rs575389921	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33346860	TTCTCACTCATGCTT[A/G]TCCTTCAACACTTTA	4799
rs575421585	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33334513	ACAAAATTAATACAC[C/T]TATGAAGTTTAAAAA	4799
rs575427098	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33347572	AGGGAACACTTTTAC[A/G]CTGCTGGTGGGAATG	4799
rs575538935	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33368195	AGCCGAGATCGCACC[A/G]CTGCACTCCACCCTG	4799
rs575705154	snp	C/T	0.000511024	0.0159766	intron-variant	NFX1	GRCh38.p7	9:33338488	GTCTGGTTTTTTTTT[C/T]CTTTTTAATTTGCCA	4799
rs575739806	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33310915	CTGTGGTGATAATGA[G/T]GTCGATTTTTTGCAC	4799
rs575744565	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33325332	GAACACATCACAACC[A/G]GAAGGCAGTAGGATG	4799
rs575777380	snp	C/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33302733	GGAGTGCAGTGGCAC[C/G]ATCTCGGCTCACTGC	4799
rs575863603	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33367135	CTCTGTCCTCTTGGC[A/G]TGGGGAAAACAGAAA	4799
rs575930472	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33320106	AGCTGGGATTACAGG[C/T]ACCTGCAATCATGCC	4799
rs576009605	snp	A/G			downstream-variant-500B	NFX1	GRCh38.p7	9:33371567	AAGATTAAAGGAGTA[A/G]TACACGTGGAGGTAC	4799
rs576021225	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33363663	AATTTTAACATTTGT[A/G]TGTCTATTTTATGTA	4799
rs576022340	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33290785	TTCTTGGACTAGATG[A/G]TGAAGCCCAGTAGCT	4799
rs576024951	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33329426	ATCCAGTGTGGCCAG[C/T]CTGCTCCTAAATCAC	4799
rs576063727	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33336246	TTTGAGATGGAGTCC[C/T]ACTCTGTTGCCCAGG	4799
rs576105699	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33323178	CCCTAAGGTTGTGCC[A/G]TCCAAAGAGTGACAC	4799
rs576107392	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33314001	ATTTTTTTTTTCTTT[C/T]TGAGATAAGTCTCAC	4799
rs576114166	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33303345	AAGGTGGTCTGCGGG[A/G]CATGTTTTAGAAGTT	4799
rs576127968	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33326282	GTGTGGTGTGGTGGC[A/G]TATGCCTGTGATCCC	4799
rs576138107	snp	A/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33322396	AGTGTGGACAAGAAG[A/T]TGGGGCTTCTTCTCC	4799
rs576140720	snp	C/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33298929	AAGGTAACAATTGGA[C/T]AGATTTTGGATGTAT	4799
rs576167785	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33307413	AAGGGTGATATGGGA[C/T]CTCAGTAAATGGTCT	4799
rs576177456	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33306588	AATTGCCCAAGTGAG[A/G]ATGAATTCCTCAAGG	4799
rs576237405	snp	A/T			intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33350209	CTTGGGAGGCTGAGG[A/T]AGGAGAATCGCTTGA	4799
rs576237882	snp	A/G			intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33365344	GGCACGGTGGCTCAC[A/G]CCTGTAATCCCAGCG	4799
rs576276387	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33343004	TTTTTTAAAGTTACT[G/T]CTAATGCTGTGTTGT	4799
rs576306949	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B, nc-transcript-variant	NFX1, LOC105376018	GRCh38.p7	9:33348821	ACCAGACGTGGTACA[C/T]ATTTTTCCTTGCTGT	4799
rs576328371	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33333090	ACCTCAAGTGATCCA[C/T]CCGCCTCGGCCTCCC	4799
rs576343762	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33349448	GTAGAATGGGTAAGT[A/G]TTTAATGATTGAGAA	4799
rs576361087	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33315125	CAGGTACTTGGAGGC[C/T]GAGGCAGGAGAATCG	4799
rs576380208	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33312639	ATTTCGGGAGGCCGA[A/G]GTGGGTGGATCACTT	4799
rs576399006	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33356001	TTCTGTTGGATATAA[A/G]CCAGAAGTAGAATTG	4799
rs576453124	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33357763	GTTGACCAGGGTGGT[C/G]TCAAACTTCTGGCTC	4799
rs576487282	snp	A/G	0.00279162	0.0372561	intron-variant	NFX1	GRCh38.p7	9:33355214	TTTAGTTAACTTTTC[A/G]TTGAAGTTTAGCATA	4799
rs576488271	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33319698	TATTTTTAATAGAGA[C/T]GGGGTTTCACCATGT	4799
rs576573860	snp	A/C	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33368789	CACCATGAAGGTCAC[A/C]GCACTTAGTGTTCCT	4799
rs576599442	in-del	-/G	0.00398564	0.0444627	intron-variant	NFX1	GRCh38.p7	9:33297305	GCCACCATCTACCCA[-/G]GGCCTGTTTTTACAC	4799
rs576623068	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33335501	GCCTCCCAAAGTGCT[A/G]GGATTACAGTCATGA	4799
rs576680067	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33290723	GGCGTAGGATAGTGG[C/T]TCGGAAGGGCCAAGC	4799
rs576717289	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33297992	ATTCTCACATTATTC[A/G]TATCATTTTTGAGAA	4799
rs576767065	snp	A/C	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33360340	AAAAATCTAGAAATG[A/C]TGACAATAACAGTAT	4799
rs576797570	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33369057	CGTTTATCCCATGCT[A/G]TCTTTTTTCTTTTTT	4799
rs576852571	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33297367	GGATTATTCTTGGAA[C/T]CTCAATGTATATGTG	4799
rs576865754	snp	A/G	0.00199481	0.0315187	intron-variant	NFX1	GRCh38.p7	9:33361936	AAGACCAGCCTGGGC[A/G]ACATAGCAAAACCCT	4799
rs576890714	snp	A/C	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33327519	ACAGGTGGGCGCCAC[A/C]ACGCCTGGCTAATTT	4799
rs576905955	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	NFX1	GRCh38.p7	9:33290375	CCATCCAGCTACTAG[C/T]CTCCTCCTCCCGCCC	4799
rs576952447	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33336096	TCTTGTGTTTAATTT[C/T]TTTGAAAAACTGCCA	4799
rs576954551	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33328791	TATGGGAAGTGGTTG[C/T]GGCACTCAAGGTCCA	4799
rs576988977	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33335452	TGCCCAGGCTGGTCT[C/T]GAACTCCTGGCCTCA	4799
rs577027763	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33369685	GAATTTGTTATCTCA[C/G]AGAATAAAATTCCCC	4799
rs577066016	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33363573	ACTGGTGTGAGCCAC[C/T]GCACCCAGCCAAGAA	4799
rs577069670	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33321435	GCTTAGGTCTTTTGT[A/G]TCTCACTCAGTAGGA	4799
rs577127395	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33305611	CTAAATAATTTGGGA[C/G]TTATAATCCAGATGA	4799
rs577131883	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33355781	TCCAGAGTAGTTGGC[A/G]TTACAGGTGTGTACC	4799
rs577162151	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33311732	TAGTTTTTGTATTTT[C/T]AGTAGAGATGGGATT	4799
rs577194232	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33320117	CAGGCACCTGCAATC[A/G]TGCCCAGCTAATTTT	4799
rs577269801	snp	A/C	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33368074	ACCCATCTCTACTAA[A/C]AATATAAAAAAGTAG	4799
rs577283545	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33324437	ACACCTGTGATCCCA[C/G]CTACTCAGGAGGCTG	4799
rs577320206	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33358245	TTCTCCTGCCTCAGC[A/G]TCCCAAGTAGCTGGG	4799
rs577321902	snp	A/C	0.0023933	0.0345097	intron-variant	NFX1	GRCh38.p7	9:33323763	ATCTCAAAAAAAAAA[A/C]CAAACAAAAAAAAAC	4799
rs577346241	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	NFX1	GRCh38.p7	9:33289671	TTCCTCCCCTGCCCT[G/T]CCCTGAGCTGCATGG	4799
rs577369914	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33345938	CATCATTTCATTTTA[C/G]CAAATACCAGAGGCA	4799
rs577371362	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33339268	TCTACAGTTCCAAGT[C/T]GGTGGGGAGGCCTCA	4799
rs577414423	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	NFX1, LOC105376018	GRCh38.p7	9:33348730	GTCCAATAAGAAATG[C/T]ATATTTATTGTACAG	4799
rs577432449	in-del	-/A			intron-variant	NFX1	GRCh38.p7	9:33368236	GACAGACTCCATCTC[-/A]AAAAAAAAAAGAATA	4799
rs577433646	snp	A/G	0.00318978	0.0398085	intron-variant	NFX1	GRCh38.p7	9:33297390	TATATGTGAAGCAAA[A/G]CAATGTTATACCAGA	4799
rs577478448	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime, downstream-variant-500B	NFX1, LOC105376018	GRCh38.p7	9:33348351	AGCAAGACTCCGTCT[C/T]GAAAAAAAAAATAAA	4799
rs577492238	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352193	ATTATTACTTAGATA[A/T]CTAATTATGGCTGTG	4799
rs577528428	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33296701	TGTACTCCAGCCTGG[A/G]TAACAGAGCAAGACC	4799
rs577531923	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352940	TTTTTTGTTTGTTTT[A/G]TTTTGTTTTATTGAG	4799
rs577567627	snp	C/T	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33303988	AAATTACCAATGGGC[C/T]GGGCTTAGTGGCTCA	4799
rs577595854	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33307571	TCACAGTGGCAGGGC[A/G]TGGATGGTGGAGCTA	4799
rs577596325	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33316688	AGCATTCTTTTTGGG[G/T]CTTTATTCATATGTT	4799
rs577606790	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33359174	TTTATTGTCAATTCC[C/T]GTTATTTTTTTCCTT	4799
rs577610592	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33297474	ATTATCACAATGTAG[C/T]GGCTTATGATAACAC	4799
rs577628307	snp	A/G	2.38604e-05	0.00345393	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33364831	GCTTGATGAAAAAAA[A/G]AAAGCAATCAAGTCC	4799
rs577630958	snp	G/T	0.00199481	0.0315187	intron-variant	NFX1	GRCh38.p7	9:33298881	GTTCAGGTAGGAGAT[G/T]ATGGAGACTTAGACT	4799
rs577638769	in-del	-/AAG			intron-variant	NFX1	GRCh38.p7	9:33298163	CTAAAAAGAAATATT[-/AAG]AAGGTTAAGAAGACA	4799
rs577668318	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33365503	ATCCCAGCTACTCAG[A/G]GGGCTGAGGCAGGAG	4799
rs577695344	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33336689	CACTGCAGCCTTGAT[C/G]TCCTGGGCTCCAGTG	4799
rs577700627	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33326487	TACTCAGGAGGCTGA[A/G]GTGGAAGGATCACTT	4799
rs577890526	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33293987	CAATAAGTTGGACAG[G/T]TGGACTTTAACCCAT	4799
rs577929396	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33293235	TCAGTTTTCTCATCA[A/G]GAATGTAAGGATTAA	4799
rs577959624	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33292286	TCCCATTCCATGTTC[A/G]TATTTTAGCATCATC	4799
rs577966450	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33300885	CGAGCCTCTTTCTAA[C/T]CTAAATCCATGGATC	4799
rs578126447	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33349693	AAAAAAAAAGAATTG[G/T]GGGTTCTATCCCCTG	4799
rs578154808	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33350392	GTTGCCCTCCACCCC[A/G]CATCTATAAGAATTA	4799
rs578195715	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33336792	TTTAATTAAGTTTTA[A/G]AAACTTAATTTTTAA	4799
rs745321036	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33314668	GATGACAGAATGAGG[C/G]TCAGTCTAAAATAAT	4799
rs745348931	snp	A/G	1.65056e-05	0.00287272	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33364841	AAAAAAAAAGCAATC[A/G]AGTCCTGGAAACACT	4799
rs745400837	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33359985	TGTGTAGAAGGTAAT[A/G]TGATGACTAGTAGTG	4799
rs745401977	snp	A/C	0.000181346	0.00952051	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33366644	GGAAAGAATAGTAAG[A/C]AAAGCCACAGCTTCC	4799
rs745439942	in-del	-/G	1.6476e-05	0.00287014	intron-variant	NFX1	GRCh38.p7	9:33318843	CAAGTAAGGTTTTAC[-/G]TTTTCTTCAGTTGAA	4799
rs745467861	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33341297	TGTGCAGGGAAACTC[A/G]GCCTTATAAAGCCAT	4799
rs745469756	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33309076	TAAGAAGTTAATCCT[A/G]GCTGGGCGCGGTGGC	4799
rs745508041	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33293949	AAGGCTAAAAGCAGG[C/G]ACGTGATATCCCTAA	4799
rs745515973	snp	G/T	1.64893e-05	0.0028713	utr-variant-5-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33290523	GGGCACGTGACCTGG[G/T]GACAGTGCTGACTTG	4799
rs745526965	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33328020	TTCTGTGTTTTTGTT[A/G]TTTGTTTTGAAACAG	4799
rs745552898	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33326693	CACTGCATTCCAGCC[A/T]GAGTGACAAGAGTGG	4799
rs745582055	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33341094	CACTCTGCTGGTACC[A/T]GTTTACTGTATTAGT	4799
rs745591155	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33336589	GTGATGTCTCTGATA[C/T]CTCAATGTTAGGTTT	4799
rs745619482	snp	C/T	1.64789e-05	0.0028704	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33307214	GTAAAGAATCCTGAG[C/T]GGAGCAGAAATGAAA	4799
rs745647737	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33368933	GTTCTGGTCAGCACA[A/G]TCTGCAAATCCATAT	4799
rs745667689	snp	C/G	1.95574e-05	0.00312703	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33351805	GGTGGGTATTTCTGG[C/G]CACAGATGCAGCATT	4799
rs745692773	snp	A/G	1.65559e-05	0.00287709	intron-variant	NFX1	GRCh38.p7	9:33328693	GGTAAATCCTAAACA[A/G]TGCTAGAGTTGTTGC	4799
rs745714098	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33336416	AGATGGGGTTTTACC[A/G]TGTTGGTCAGGCTGG	4799
rs745726967	snp	A/G	1.67666e-05	0.00289534	intron-variant	NFX1	GRCh38.p7	9:33354944	CTTGAGCTCTGTGAA[A/G]TTAATGGGAGGGAGC	4799
rs745735902	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33291169	CCCTCCTGGAGTTGC[C/T]TCAGTGTGTAGAGAC	4799
rs745739635	snp	A/C			upstream-variant-2KB	NFX1	GRCh38.p7	9:33290407	ACACCTGGCGCGTCT[A/C]TCTGACGTCACGAAC	4799
rs745774556	in-del	-/A			intron-variant	NFX1	GRCh38.p7	9:33315226	GCGGAACTCTGTCTC[-/A]AAAAAAAAAAAAAAA	4799
rs745797255	snp	A/G	1.65781e-05	0.00287902	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33294805	TGGATTAGAGAGCTC[A/G]ACCAGATCAGAGAGT	4799
rs745813302	in-del	-/GGTTGAAGTGA			intron-variant	NFX1	GRCh38.p7	9:33318269	AACCTGTGCTTCTTG[-/GGTTGAAGTGA]GGATGGGAAATCCAG	4799
rs745814185	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33338788	GCCTCACCCAGGTTA[A/G]GAAGTCAGCCAGTGG	4799
rs745823910	snp	A/G			upstream-variant-2KB	NFX1	GRCh38.p7	9:33289083	ATATCGACACCCCCA[A/G]CTAAAGCACAAGCAC	4799
rs745829305	snp	G/T			intron-variant, downstream-variant-500B	NFX1, LOC105376018	GRCh38.p7	9:33348928	TTTTTGCATCATGAC[G/T]TATTGGCCAACATTT	4799
rs745893542	snp	C/G	1.65272e-05	0.0028746	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294977	TGTGAATGGAGTAAC[C/G]GAACAACTCCAAAAC	4799
rs745894460	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33330115	GGATAGTTTTCATCA[C/G]ACTTTATGTTATAAA	4799
rs745906151	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33344313	TGCTCCCGGCTCAGG[A/G]GCTGGTTCTCTGAAG	4799
rs745970544	snp	C/T	9.88517e-05	0.00702966	intron-variant	NFX1	GRCh38.p7	9:33344200	CCAGGTGAGTACCAA[C/T]TTGTCTTCACACTTC	4799
rs745984486	snp	A/T	1.66034e-05	0.00288122	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33364042	TTCATATCAGTGAGG[A/T]TTCTGATCCTTTCAA	4799
rs745996104	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33296715	GATAACAGAGCAAGA[C/T]CCTGTTTTGCGGGGG	4799
rs746009136	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33344573	TATTAAAATTAAGAA[A/C]ATAGAGGCCAGGGCC	4799
rs746039618	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33301849	GGCCAAGGCAGGCGG[A/G]TCATCTGAAGTCAGA	4799
rs746122019	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33308200	TAATCCCAACACGTT[A/G]GGAAGCCAAGGCAGG	4799
rs746175912	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33304173	AGGCTGAGGCAGGAG[A/T]ATCGCTTGAACCTGG	4799
rs746182233	snp	A/G			intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33351308	TAAAAAAAAATTCAA[A/G]AATTAGCTGGGCGTG	4799
rs746197424	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33301424	GCATCTCAAGCAGGT[C/T]AATTAATTCTCTCTT	4799
rs746203314	snp	C/G	0.000115495	0.00759831	intron-variant	NFX1	GRCh38.p7	9:33367482	CACAAACAATTCTCA[C/G]TTTTCAATGCTTGGT	4799
rs746224922	snp	A/G	0.000115362	0.00759393	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33301300	AACAGAAAAATACGA[A/G]TGCATGGTGTGCTGT	4799
rs746256176	snp	A/C	1.64735e-05	0.00286993	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33367570	CTTGAAAGGGAAATG[A/C]AGGCACGGCCTCCAC	4799
rs746325425	in-del	-/G	1.65474e-05	0.00287636	intron-variant	NFX1	GRCh38.p7	9:33347006	GGCTTTATTTAGAAA[-/G]TATTCCTAAAGTTAC	4799
rs746362534	in-del	-/ATTTTTGT			intron-variant	NFX1	GRCh38.p7	9:33355811	CACCATGCCCAGCTG[-/ATTTTTGT]ATTTTTAGTAGAAAT	4799
rs746395666	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33297603	CATCTGAGGCTCAGG[A/G]TTCTCTTTCAGTCAC	4799
rs746426321	snp	A/G	3.43619e-05	0.00414485	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33294463	TGAATTCATTCCTCA[A/G]GAGAAAAAAAATTCT	4799
rs746432575	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33331223	TTTAACTAGATTTTT[C/T]ATGAATATGGATTTT	4799
rs746447574	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33326534	GGCCAGCCTGGGCAA[C/T]GTAGTGAGATTTAAT	4799
rs746455145	snp	A/G	1.73174e-05	0.00294251	intron-variant	NFX1	GRCh38.p7	9:33338622	GCATAATCAGATTCC[A/G]TTCATCCAGGTGCTG	4799
rs746464469	snp	C/G	1.64741e-05	0.00286998	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33313695	TCTCAGTCCACTGTT[C/G]TAACCCATGTGAGAA	4799
rs746485504	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33358522	TCAAAAAAAAATGCA[A/G]ATTACAAGGACTTCA	4799
rs746486834	snp	C/T	1.80651e-05	0.00300536	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33364722	GGAAGGACTTAAAGT[C/T]TGTCAGTGACGTTGA	4799
rs746515435	snp	A/T	1.76527e-05	0.00297087	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33342801	TCCGTTGTGGCCTTC[A/T]TAGGTGTGAAGAACC	4799
rs746546115	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33356617	TATTATCTAGAAACT[C/G]TGTTATTTTACCTTT	4799
rs746572472	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33315098	GGGCGTGTTGGCGGG[C/T]GCCGGTAATCCCAGG	4799
rs746649702	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33325231	GATAAGGAGAAAGTC[C/T]TGAAAGCAGCAAGAG	4799
rs746687666	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33305101	TTTATTGAGAACTTA[C/T]TAATGTTCAAGGCAC	4799
rs746691798	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33291897	GACAGAGTGTGACTT[C/T]GTCTCAAAAAAAAAA	4799
rs746692969	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33338962	GCTTCAGGTTTCATG[A/T]ACTGCTTAGGTCAGG	4799
rs746694318	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33312687	ACCAGGTGGGCCAAC[A/G]TGGTGAAACCCCGTC	4799
rs746710711	snp	A/G			intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352557	TCTCTAGTCTCTGCT[A/G]TGGTTTAAGAGAGGA	4799
rs746724780	snp	C/T	1.67936e-05	0.00289767	intron-variant	NFX1	GRCh38.p7	9:33313845	TCTTTTCTGGAACCT[C/T]ATTAATGATTGTCTT	4799
rs746750324	snp	C/T	1.67329e-05	0.00289243	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33351724	CCCCAGAGCTGACTG[C/T]GGTCACCCGTGTATG	4799
rs746763042	in-del	-/A	3.29576e-05	0.00405928	splice-acceptor-variant	NFX1	GRCh38.p7	9:33367513	GTTTTGACTTTTATC[-/A]GGGGGAAGTCCGTTT	4799
rs746771449	snp	G/T	1.64787e-05	0.00287038	intron-variant	NFX1	GRCh38.p7	9:33319178	TATTGTAAATGGTTG[G/T]CAGCAGTGAGTGTTT	4799
rs746857675	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33341699	TTTTGAGGCCGAGGT[A/G]GGTGGATCTTGCTTG	4799
rs746891385	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33299760	ATTTAACAAATATTT[A/C]ATGGAGCACCTAGTA	4799
rs746915708	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33314379	AAGACCAAAATAATC[C/T]TTTTAAAAATGAACT	4799
rs746933024	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33369285	TGTTAGGATGGTCTC[A/G]ATCTCCTGACCTCGT	4799
rs746943126	snp	A/G/T	6.6127e-05	0.00574976	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33366603	AGAATGATATGATCA[A/G/T]TCAGTCATCTTTTCC	4799
rs746985970	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33346124	CCTTGGGGATCTTAG[C/G]ATAGCCCTCCCAGCG	4799
rs747002301	snp	A/G	1.64762e-05	0.00287016	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33328646	TGCTCTCGCACATCA[A/G]TTATTTCCTGCAGAT	4799
rs747039532	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33355257	TGGAAGTGTGCAGAT[C/G]AGTGAATCGTCACTA	4799
rs747060175	snp	C/T	1.95276e-05	0.00312465	utr-variant-3-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33370029	GGTATAGTGGAGACT[C/T]ATTTGCCAGCAGATA	4799
rs747064844	snp	C/T	6.61474e-05	0.00575059	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294689	AAATCGCCCAAGAGC[C/T]ATGGCCTTCAGAATC	4799
rs747075322	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33354510	GGCTGTTAAGAGGGG[C/T]ACCTGTGGAGCATTT	4799
rs747121493	snp	A/G	8.25576e-05	0.00642433	intron-variant	NFX1	GRCh38.p7	9:33354226	TGCCTTCTTTCTTCA[A/G]TTAGACTTCAATTAG	4799
rs747121753	snp	A/G	1.65089e-05	0.00287301	intron-variant	NFX1	GRCh38.p7	9:33307187	TCTCTGATCTGATAT[A/G]TTCTAGGCAAGGTAA	4799
rs747135716	in-del	-/GT			intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33349741	AAAGGACAGGACTGC[-/GT]GAAGCTGTGGAGACC	4799
rs747224012	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33306664	CTGAGTCCATGGAAG[A/T]TGTGCCATGAAGATT	4799
rs747261162	snp	C/T	1.64754e-05	0.00287009	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33344186	ATGAGTGTGACCATC[C/T]AGGTGAGTACCAACT	4799
rs747279188	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33321273	CAGGTTAAGGGATAA[A/G]AGGGTACCTGCTATA	4799
rs747281736	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33331122	AGTGAACCGAGATTG[C/G]ACCACTGCGCTCCAG	4799
rs747289879	in-del	-/AT	1.64795e-05	0.00287045	frameshift-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33311157	CTTTATGACAAAAAC[-/AT]GTGAATGTGGACGAA	4799
rs747319326	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33316819	ATATTTCTGTCTCTC[A/G]TGCCTAGGAGAGCTT	4799
rs747333586	snp	A/G	8.25008e-05	0.00642212	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33295400	GGCAAACAGAACCAT[A/G]TGCTAAAGAATGTGG	4799
rs747345263	snp	G/T	3.29457e-05	0.00405854	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33318804	TGATGGATTTGGGGA[G/T]TTCAGCTGTTTAAAG	4799
rs747382309	in-del	-/TTTTA			intron-variant	NFX1	GRCh38.p7	9:33354072	CTTTTTCCCTTTCTT[-/TTTTA]TTTTATATTTCAGAA	4799
rs747412323	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33360759	TTGAATTAGTGGCCA[A/G]CTAACCAAAACATCA	4799
rs747416001	snp	C/G	1.64806e-05	0.00287054	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33347060	TTCTTGTCATAGTGA[C/G]GAGAAGTGTCCCCCT	4799
rs747481308	snp	C/T	0.000145826	0.00853766	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352443	GTTTCCAAAAGGGGG[C/T]ATTGTGGACGGGGCA	4799
rs747537492	snp	A/G	3.56875e-05	0.00422404	intron-variant	NFX1	GRCh38.p7	9:33366816	GAACTCCTAAGCAGG[A/G]CAAACTGGACCCAAG	4799
rs747554251	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33330194	CCTGCTCTTTGACCT[A/C]CTTAGTCATTTTAGT	4799
rs747572562	snp	C/G	1.65059e-05	0.00287275	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33301274	ACAGGTTCTCTAATT[C/G]AACAACTAACAACAG	4799
rs747601126	snp	C/T	1.8104e-05	0.0030086	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294426	ATGTCCTAGGTACTT[C/T]TAAATTCAATACAGA	4799
rs747605590	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33343188	TTTGCAAACTTTTTG[A/G]TTGTAGGGCTCATTT	4799
rs747679809	snp	C/T	1.64868e-05	0.00287109	intron-variant	NFX1	GRCh38.p7	9:33338490	CTGGTTTTTTTTTTC[C/T]TTTTAATTTGCCACA	4799
rs747729005	in-del	-/T	1.65214e-05	0.0028741	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33366609	TATGATCAATCAGTC[-/T]ATCTTTTCCCTCAAT	4799
rs747736111	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33360659	CCTGTGTGTATATAT[A/G]TGTATGTGTGTATAT	4799
rs747745377	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33359064	ATAATTATTGACTTA[C/T]TTAGCAACCTCGCTA	4799
rs747780580	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33304005	GGCTTAGTGGCTCAC[A/G]CCTGTAATCCCAGCA	4799
rs747785930	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33336891	CGGATCACTTGAGGT[A/C]AGGAGTTCAAGACTA	4799
rs747835676	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33318196	AATTTTTAAATTTCT[C/T]TTTGGCAACGGGGAC	4799
rs747840802	snp	A/G			intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33350197	TAGTCCCAGCTACTT[A/G]GGAGGCTGAGGTAGG	4799
rs747841095	in-del	-/C			intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33353186	CCTCTTTCTTTTTTT[-/C]CTCTCTTTTGGTCGT	4799
rs747939329	snp	G/T	1.64776e-05	0.00287028	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33313671	ACACAGTTCGCTGTG[G/T]TCAGGCTGTCTCAGT	4799
rs747975920	snp	A/G	0.000148747	0.00862272	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33294994	AACAACTCCAAAACC[A/G]GAGGATGCTGGACCC	4799
rs747981212	snp	C/G	3.71637e-05	0.0043105	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33364816	ATTTCTCTAAGGCCA[C/G]CTTGATGAAAAAAAA	4799
rs748007302	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33311791	CTATTGACTTCGTGA[A/T]CCACCCGCCTCGGCC	4799
rs748033119	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33313121	GAGCTAGGACCAGAA[C/G]CCAGATCTTCTAACT	4799
rs748037181	in-del	-/AA	1.67382e-05	0.00289289	frameshift-variant, nc-transcript-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33351726	CAGAGCTGACTGTGG[-/AA]TCACCCGTGTATGGC	4799
rs748040227	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33292529	GTGGTGACTAGACAT[C/T]CTGTTTACTAACTTC	4799
rs748041375	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33315662	GAGGCCAGGGCAGGT[C/G]GATCACTTGAGCCTA	4799
rs748058720	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33325181	TAGGAAAGAGATCCA[C/T]ATCTAGACATATAAT	4799
rs748101287	snp	A/G	1.64768e-05	0.00287021	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33319086	ACCCTGTGCCTTCAT[A/G]TGGAAAAGTGTGCGG	4799
rs748127878	snp	C/T			intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33353131	TTTCTTCCCTAACTT[C/T]AGTGTGTAAAATAAC	4799
rs748154598	snp	A/T			synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33294421	TTTTTATGTCCTAGG[A/T]ACTTTTAAATTCAAT	4799
rs748161391	snp	C/T	1.64811e-05	0.00287059	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33351601	GGTTGATATCTCTTG[C/T]GGATTACCCTGCAGT	4799
rs748243324	snp	A/G	1.77068e-05	0.00297541	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33354102	ATAGCTGCAATCTCC[A/G]TGGCCTCTAAGATAA	4799
rs748243837	snp	C/T	1.73087e-05	0.00294177	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33369910	TTGTTTTTCAGGAAT[C/T]CTGGGAGCAGTAATT	4799
rs748248803	snp	A/G	1.93366e-05	0.00310933	intron-variant	NFX1	GRCh38.p7	9:33354210	TTAAAATGCATATAT[A/G]TGCCTTCTTTCTTCA	4799
rs748250698	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33342303	CGTCTCTACTAAAAA[C/T]ACAAAAAAATTAGCC	4799
rs748269950	snp	A/G	1.733e-05	0.00294358	intron-variant	NFX1	GRCh38.p7	9:33319161	GTTGGCTTTAAAAAT[A/G]TTATTGTAAATGGTT	4799
rs748314218	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33333757	AGAAGAGTGGCCGTT[C/T]GGGAGGTACCCAGCA	4799
rs748325477	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33291557	AAGAAGACCATATAT[A/G]TATTTGTATACTGGG	4799
rs748341054	in-del	-/TTG			intron-variant	NFX1	GRCh38.p7	9:33320469	AATTGTTGTATCTGC[-/TTG]TTGAAGCTTTTTGTT	4799
rs748360812	snp	G/T	1.6522e-05	0.00287414	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33294667	TTTCCAGTCCTCTCC[G/T]TGTAATAAATCGCCC	4799
rs748365178	snp	C/G	1.65427e-05	0.00287595	intron-variant	NFX1	GRCh38.p7	9:33307173	TTTGTACCATTGACT[C/G]TCTGATCTGATATGT	4799
rs748421806	snp	C/G	1.64817e-05	0.00287064	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294599	GAAATCTCTGCTGTT[C/G]ATCAGCATAGTTATC	4799
rs748452147	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33332829	ATATGGATGTTCACT[G/T]TAAAATACTTTGAAC	4799
rs748479632	snp	G/T	1.64746e-05	0.00287002	intron-variant	NFX1	GRCh38.p7	9:33344038	CCCAAACTCAGAAAG[G/T]ATTCTTTTGTTTTAC	4799
rs748492217	snp	A/G	3.29582e-05	0.00405931	intron-variant	NFX1	GRCh38.p7	9:33318703	ATACATGTTACTAAC[A/G]TTTTGTTTTTGAAAT	4799
rs748556877	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33347355	CACTACCACAATCAA[A/G]ATATAGAACAGTTCA	4799
rs748566256	snp	C/T	1.67478e-05	0.00289372	intron-variant	NFX1	GRCh38.p7	9:33354922	CTGCTTTTTTAATCT[C/T]CTTGCCCTTGAGCTC	4799
rs748653854	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33341374	GACCTCCCCCACCAT[A/G]ATTTAGTTAACTCCT	4799
rs748687488	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33306562	TGGGGATGGCTGCAA[G/T]TTAGTGTGCAAATTG	4799
rs748700380	snp	C/G	1.64898e-05	0.00287135	utr-variant-5-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33290531	GACCTGGTGACAGTG[C/G]TGACTTGGCTGTACA	4799
rs748704744	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33340216	CATCCAGGCATTTCC[A/G]TACATCTTTTGAAAC	4799
rs748716336	snp	C/T	3.29571e-05	0.00405924	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33366659	AAAAGCCACAGCTTC[C/T]CTCCCATGAACAGAG	4799
rs748719024	snp	A/G	1.64901e-05	0.00287137	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33366723	TTTATGGCCTGGAGA[A/G]CGTGAGCTATGACAG	4799
rs748719247	snp	C/T	1.64727e-05	0.00286986	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33318789	CGATGTAGGAAAGTC[C/T]GATGGATTTGGGGAT	4799
rs748721204	snp	A/T	1.64765e-05	0.00287019	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33295274	AGACCAGCAAAATCT[A/T]CCTGTGACAGTGAGA	4799
rs748754825	in-del	-/AGCCCTGCAAGC	1.65124e-05	0.00287331	cds-indel, nc-transcript-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33351683	AGTGTCTTGTGGATG[-/AGCCCTGCAAGC]AGCCCTGCAAGCAGC	4799
rs748771170	snp	C/T	6.15176e-05	0.00554572	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352432	GAACAGAGGTGGTTT[C/T]CAAAAGGGGGCATTG	4799
rs748791183	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33335421	TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT	4799
rs748801998	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33362241	ATTAAAAATAGAACT[A/G]CCATATGATCCAGCA	4799
rs748810142	snp	A/C			intron-variant, downstream-variant-500B	NFX1, LOC105376018	GRCh38.p7	9:33349182	TATGTGCTAGGTAAC[A/C]GGCTAGGTTTGGGTG	4799
rs748822455	snp	A/G/T	6.73042e-05	0.00580071	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33351733	TGACTGTGGTCACCC[A/G/T]TGTATGGCACCCTGC	4799
rs748881696	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33335987	TTGTGAATAGTGCTG[C/T]TATGAACATTTGTAT	4799
rs748883748	in-del	-/TT			intron-variant	NFX1	GRCh38.p7	9:33302359	TCTATCTAACTGTAT[-/TT]TTTTTTTTTTTTTTT	4799
rs748912654	in-del	-/G	1.65847e-05	0.0028796	intron-variant	NFX1	GRCh38.p7	9:33328542	TGAAAATGAGTAGTT[-/G]GCAGTTTTCATTTCC	4799
rs748942553	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33316505	AATTTCTGTGGATCC[C/G]AGTCTCTTCCTCCTT	4799
rs748994943	snp	C/T	3.29641e-05	0.00405968	intron-variant	NFX1	GRCh38.p7	9:33311213	TAAAGAAGACCTCAG[C/T]TTTCACATGCATGAT	4799
rs748998437	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33360669	TATATATGTATGTGT[A/G]TATATCTCTATTGTA	4799
rs749019010	snp	A/G	1.65712e-05	0.00287843	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33364059	TCTGATCCTTTCAAT[A/G]TACGTTCTTCAGGGT	4799
rs749050514	snp	C/T	4.96257e-05	0.004981	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294867	AGAGTGAGAAGGAAG[C/T]TGTGGGTGCAGATCC	4799
rs749052163	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33355752	CGGGTTCAAGCGATT[A/C]TCTTGCCTTAGCCTC	4799
rs749056992	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33325100	AATATTTAATGAAAT[A/G]ATAGATAAAAACTTT	4799
rs749063841	snp	A/G			missense, nc-transcript-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352680	GTGGACGAAGAAAAG[A/G]GATGGTGATTTGCTC	4799
rs749073168	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33356744	CGAGTACCAAGATTG[A/T]CCTTTTCCCAGCACT	4799
rs749091213	snp	A/G	1.70124e-05	0.00291649	intron-variant	NFX1	GRCh38.p7	9:33338598	CTGTGTGGTAAGTGG[A/G]CTTATTAGGCATAAT	4799
rs749119528	snp	C/G	1.65658e-05	0.00287795	intron-variant	NFX1	GRCh38.p7	9:33311092	GTTTATTCAGTGAAA[C/G]CTTTCTCTTTCAGTC	4799
rs749178270	snp	C/T	2.65565e-05	0.00364384	intron-variant	NFX1	GRCh38.p7	9:33364661	GGTGAAAGGGGTTCT[C/T]AGAAGGGCAGGGACA	4799
rs749180683	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33324161	AGGCAGGCAGATCAC[C/T]TGGGATCAGGAGTTT	4799
rs749224231	snp	C/T			utr-variant-5-prime, upstream-variant-2KB	NFX1	GRCh38.p7	9:33290453	GGGCTGCGCAACCTC[C/T]GTGGCCGTCTACACG	4799
rs749231661	snp	C/T	3.30524e-05	0.00406511	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294981	AATGGAGTAACCGAA[C/T]AACTCCAAAACCGGA	4799
rs749254119	snp	C/G	1.64882e-05	0.00287121	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33347098	TCCTAACTCAGAAGT[C/G]GTGCATGGGCAAGCA	4799
rs749254397	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33369299	CAATCTCCTGACCTC[A/G]TGATCCGTCCGCCTT	4799
rs749271451	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33315852	AGCTGAGATCATGCT[A/G]CCGCACTCCAGCCTA	4799
rs749297726	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33332605	CAAAATTCAGTGAAG[A/G]CATACTTAAGATTTG	4799
rs749349994	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33364655	AGGATGGGTGAAAGG[A/G]GTTCTCAGAAGGGCA	4799
rs749397674	snp	A/C	6.5925e-05	0.00574092	intron-variant	NFX1	GRCh38.p7	9:33367504	ATGCTTGGTGTTTTG[A/C]CTTTTATCAGGGGGA	4799
rs749469629	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33329310	TTTTATTGGTGCTCT[A/G]TTGTGCAATCATAGT	4799
rs749549933	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33296733	TGTTTTGCGGGGGGA[A/T]AAAAGTTACTTTAGT	4799
rs749569134	snp	C/T	1.6569e-05	0.00287824	intron-variant	NFX1	GRCh38.p7	9:33301455	CTGAGTAGTTATTCT[C/T]CCCTATTTGATACGT	4799
rs749619721	snp	A/G	1.6554e-05	0.00287693	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294494	GGTCTAAATTGTGGG[A/G]CTCAAAGGAGACTAG	4799
rs749643176	snp	C/T	1.7693e-05	0.00297425	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33342806	TGTGGCCTTCATAGG[C/T]GTGAAGAACCTTGTC	4799
rs749643279	snp	A/T	0.000148252	0.00860838	intron-variant	NFX1	GRCh38.p7	9:33354197	AGCCAGGTAATTTTT[A/T]AAATGCATATATGTG	4799
rs749653888	in-del	-/AATAT			intron-variant	NFX1	GRCh38.p7	9:33353593	CATGTAGCTGCTTTG[-/AATAT]AATTGAAGAGATATG	4799
rs749676432	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33306274	CTCTGACAGAGTTGA[C/T]GTCACTGACAGAAAT	4799
rs749681973	snp	G/T			intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352841	AACGAAGTCTGTAAC[G/T]GTTGTAATCAGTTGT	4799
rs749694529	snp	G/T	3.6527e-05	0.00427343	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33354088	TTTTATATTTCAGAA[G/T]AGCTGCAATCTCCAT	4799
rs749766979	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33305284	GCCTTCTTGGAGGAG[A/G]TAGAATTGAACTGGC	4799
rs749767278	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33320870	ACATTTCTTTCAAGT[A/G]CCAGCGTGAATCAGT	4799
rs749814602	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33319743	TCGAACTCCTGGCAC[C/T]AAGTGATCCACCCGC	4799
rs749825952	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33308717	TGAATTAGTGCATCT[A/G]TGCGGCTCGATATAG	4799
rs749842889	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33329305	TCAGTTTTTATTGGT[A/G]CTCTATTGTGCAATC	4799
rs749866424	snp	A/G	1.64746e-05	0.00287002	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33313707	GTTCTAACCCATGTG[A/G]GAATATTTTGAACTG	4799
rs749871939	snp	A/C	1.6477e-05	0.00287024	intron-variant	NFX1	GRCh38.p7	9:33344018	GTTAGTATGTACTTG[A/C]ACATCCCAAACTCAG	4799
rs749873835	in-del	-/GAAAAA			intron-variant	NFX1	GRCh38.p7	9:33345174	CTCAAAAAAAGAAAA[-/GAAAAA]GAAAAAGAAAAAAAA	4799
rs749874115	snp	A/G			intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33351368	GGGAGACTGAGATGG[A/G]AGGATCACCTGAGCC	4799
rs749907395	snp	C/T	1.64727e-05	0.00286986	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33318774	TGTGTTATGTGGAAC[C/T]GATGTAGGAAAGTCT	4799
rs749939292	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33296182	TCCGCCTCGGCTTCC[C/T]AAAGTGCTGAGATTA	4799
rs749960266	snp	A/T	0.000120839	0.00777205	intron-variant	NFX1	GRCh38.p7	9:33363990	CTCCTTTTATTTGCA[A/T]ACCTCTCTCTCTCTT	4799
rs749964248	snp	C/T	1.64732e-05	0.0028699	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33344142	TGGTACTAGGCCCCC[C/T]GAATGTACCCAAACC	4799
rs749996370	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33308770	AAAATGACAATTCTT[A/G]CTTTTACTACCCAAA	4799
rs750021585	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33343509	GATAGCCTTACACAG[A/G]AGAAGGGAAGAGTAT	4799
rs750031800	snp	A/T			utr-variant-3-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33370366	ATTTGTCCTCCTGAA[A/T]ATGCCTGAAACATCA	4799
rs750037320	snp	A/G	4.61862e-05	0.00480531	intron-variant	NFX1	GRCh38.p7	9:33295473	TGTCTTTTTAATTTA[A/G]ATTTTTAAATAAGTC	4799
rs750040440	snp	A/G	1.6522e-05	0.00287414	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294950	GGACCAAAAGTCAAG[A/G]GGAAACTCAAATGTG	4799
rs750071390	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33368799	GTCACAGCACTTAGT[A/G]TTCCTGTGGGACTGG	4799
rs750091700	snp	A/G	1.64757e-05	0.00287012	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33318916	TCTTAACAGGGACTT[A/G]AAATGCGGTAACCAT	4799
rs750118361	snp	C/T			intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33350862	CCTTATTTTAAAAAC[C/T]GAGCTGAGTGTGGTG	4799
rs750149873	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33354988	TCATTCACTCAGCAC[A/T]GCGCTGCGTCTTTTA	4799
rs750202530	snp	A/G	1.69801e-05	0.00291372	intron-variant	NFX1	GRCh38.p7	9:33366783	CCATCAGGTAGGTCA[A/G]TCCCGCCGTCAGAGG	4799
rs750288649	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33303760	TTTGAATATCTCAGT[C/T]CCCCCAAGTATTAGG	4799
rs750356191	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33363757	ACCCCCAAACTCCTC[C/T]TCCCCAAATAATCTA	4799
rs750359068	snp	A/T			intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33349886	TAGTGGCATGCCTGT[A/T]CTCCCAGCTACTTGG	4799
rs750381915	snp	C/T	1.65209e-05	0.00287405	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352746	TTAAATGTTAACAAC[C/T]GATGGCCTAGGTGAA	4799
rs750407918	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33330609	GTGTGACTGAAAATT[A/G]TAAGCAGGGTTGGGA	4799
rs750408203	snp	C/T	1.84211e-05	0.00303483	intron-variant	NFX1	GRCh38.p7	9:33294386	TGGATGAAGTTTAAT[C/T]TCTTTACTGGCATGT	4799
rs750424673	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33361722	AGGTTGCAGTGAACC[A/G]AGATCATGCTATTGT	4799
rs750441430	snp	G/T	5.22735e-05	0.00511214	intron-variant	NFX1	GRCh38.p7	9:33364153	TGTGGCTTGTCAGGG[G/T]GTTTGGTCTTTTGAG	4799
rs750456170	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33357782	AACTTCTGGCTCAAG[C/T]GAACCTCCTGCCTTG	4799
rs750471286	snp	C/T	3.45871e-05	0.00415841	intron-variant	NFX1	GRCh38.p7	9:33342727	CATTTTATGAACAAA[C/T]ATAAATCTCTTTTCC	4799
rs750479330	snp	G/T	1.64931e-05	0.00287163	intron-variant	NFX1	GRCh38.p7	9:33313647	TTTACATCTATTGTC[G/T]TTACAGGCACACAGT	4799
rs750523853	snp	C/G			downstream-variant-500B	NFX1	GRCh38.p7	9:33371216	TTTTTTTCCTCAATC[C/G]TCCTCCTCCTGTAGC	4799
rs750534278	snp	C/G	3.29538e-05	0.00405904	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33311174	GTGAATGTGGACGAA[C/G]CAGGTAAAGTTAAAA	4799
rs750544815	in-del	-/TT			intron-variant	NFX1	GRCh38.p7	9:33362692	AATAAGTTCCTGTGG[-/TT]TTTTTTTTTTTTTTT	4799
rs750549105	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33334469	CTAAAACAATAAAAC[A/C]AAATAATAAAAACAT	4799
rs750570682	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33310793	ATTTTTATCCCCACA[C/T]ACTGCTGTAAGTGGG	4799
rs750600889	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33292378	CTGCCGGTGAGCAGA[C/G]TCTGCAATGCCAGCC	4799
rs750628024	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33362007	ACACTTGTAGTGCCA[C/G]CTACTGGAGAGGTTG	4799
rs750629696	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33339401	ATCTCATGAGACTTA[C/T]TCACTATCACGAGAA	4799
rs750638766	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33324973	AACCCAACGGACAGA[C/G]AGAAAATATAATGAA	4799
rs750655337	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33291357	GGAAGCAGTGAGGTT[A/G]GTTGGTTTGTTTTAC	4799
rs750658985	snp	A/G	6.59261e-05	0.00574097	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33295191	CACCAAAACAGGAGG[A/G]CCACCGACATACAAA	4799
rs750659731	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33304784	TATTCTTGAATATAC[C/T]ACCAGAAAGGCAGCA	4799
rs750695554	in-del	-/CTCACAAT			intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352151	AGAGACACATGGTTC[-/CTCACAAT]CTGATAGGACAGATA	4799
rs750714099	snp	C/T	3.30382e-05	0.00406423	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33295040	GTGGGGGTTTTCCAC[C/T]CTGACTCTTCAGAGG	4799
rs750747817	in-del	-/GTCAGGGTGTTTGGTC	0.000120639	0.00776562	intron-variant	NFX1	GRCh38.p7	9:33364146	TCTTAATTGTGGCTT[-/GTCAGGGTGTTTGGTC]TTTTGAGATGTCATA	4799
rs750794308	snp	C/T	3.3066e-05	0.00406595	missense, nc-transcript-variant	NFX1, LOC105376018	GRCh38.p7	9:33351563	TGTCTCTCCTAGTTT[C/T]GGAGCAACATCCCCT	4799
rs750830269	in-del	-/TTT			intron-variant	NFX1	GRCh38.p7	9:33354073	CTTTTTCCCTTTCTT[-/TTT]TATATTTCAGAATAG	4799
rs750836048	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33300507	GCAGTGCTAAAAGTA[C/T]GTACTCAAAAAAGCA	4799
rs750842407	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33299095	GTTGCAAAGATAGTT[C/G]AAAGAATTCCCATAT	4799
rs750855291	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33358275	GACTGCAGGTGCCCA[C/T]CACTACACCCGGCTA	4799
rs750866215	in-del	-/AG			intron-variant	NFX1	GRCh38.p7	9:33357001	GTCTCAAAAAAAAAA[-/AG]AAAAAAAATAAGCCG	4799
rs750881272	snp	A/G	1.64779e-05	0.00287031	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33294571	TCACCTTTCCAGGCA[A/G]GTCCCTTATGATGAA	4799
rs750886482	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33317149	ATAGGCCGGGTGTAG[A/T]GGCTCACACCTGTAA	4799
rs750889635	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33332230	TTTGGAGACCAGACC[A/T]CAAAAATTGTTAGAA	4799
rs750919821	in-del	-/A/AA			intron-variant	NFX1	GRCh38.p7	9:33315890	TACCCACCTCTGTCT[-/A/AA]CAAAAAAAAAAAAGT	4799
rs750923271	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33346708	CAGAAGTGAGCAGTT[A/G]CGGTTAAAGTAGGGC	4799
rs750935554	snp	A/G	3.29669e-05	0.00405984	intron-variant	NFX1	GRCh38.p7	9:33303314	TTTACTACATACATT[A/G]TACCTCAGTTCAGGA	4799
rs750963641	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33341004	CTTCTGAGCCCTCCA[G/T]ACTGTTCCAACATCT	4799
rs750970201	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33358916	GTTGGCCAGGCTGGT[C/T]TCACATTCCTGGGCT	4799
rs750972739	in-del	-/CAGCCTGGGCGACAAGAG			intron-variant	NFX1	GRCh38.p7	9:33361742	CATGCTATTGTACTC[-/CAGCCTGGGCGACAAGAG]CAGCCTGGGCGACAA	4799
rs750973399	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33312742	TGGGTGTGGTGACAC[A/G]TGCCTGTAGCCCCAG	4799
rs750974433	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33345483	CTCTGTCTCAAAAAA[A/T]AAAGAGAGATAAAGT	4799
rs750974588	snp	C/T	1.64906e-05	0.00287142	intron-variant	NFX1	GRCh38.p7	9:33328571	CCAGCTCTTTTCGTT[C/T]TTATTAAAGATTTCA	4799
rs751013103	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33354906	AAGTAAGTAGTTGCA[G/T]CTGCTTTTTTAATCT	4799
rs751044704	snp	C/G	4.18962e-05	0.00457672	intron-variant	NFX1	GRCh38.p7	9:33342902	AGTTTTTTAGAAATT[C/G]AGACATAATATACTT	4799
rs751076597	snp	C/T	1.88397e-05	0.00306912	intron-variant	NFX1	GRCh38.p7	9:33354842	ATTTTTTTTCATTTG[C/T]TTATCAAGGCTGGAG	4799
rs751098880	snp	A/G	3.49284e-05	0.00417887	utr-variant-3-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33369980	ACGTCCAGGACTAAG[A/G]AGATCATGATGCACT	4799
rs751129925	snp	C/T	1.78334e-05	0.00298603	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33354184	AGGAAGTTCATCAAG[C/T]CAGGTAATTTTTAAA	4799
rs751147346	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33321740	TTTATTTACCTGGGT[A/G]TGGCGGCACGTGCCT	4799
rs751169794	snp	A/G	3.29451e-05	0.00405851	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33318755	GCGGCAGCACCTCCC[A/G]AGATGTGTTATGTGG	4799
rs751186673	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33293678	TTGTCTTTGTGCTTC[A/G]GGGACTGAATTGACT	4799
rs751223287	snp	G/T	3.29457e-05	0.00405854	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33344106	TTGTGGTGCATCAGT[G/T]ATTTACCCTCCAGTT	4799
rs751232643	snp	A/G			utr-variant-5-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33290499	TATTCTCGCGGCGCC[A/G]GAAGTCCGGGGCACG	4799
rs751297808	snp	C/T	3.29592e-05	0.00405938	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33295346	GAGAAATGCACTGTA[C/T]GGAGGCAGGATCCTC	4799
rs751312611	snp	G/T	1.64754e-05	0.00287009	intron-variant	NFX1	GRCh38.p7	9:33318896	AATTATGTAATAGTG[G/T]GTTTTCTTAACAGGG	4799
rs751323442	snp	A/T			missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33301304	GAAAAATACGAGTGC[A/T]TGGTGTGCTGTGAAT	4799
rs751356481	snp	A/C			intron-variant, utr-variant-3-prime, downstream-variant-500B	NFX1, LOC105376018	GRCh38.p7	9:33348645	GAACAGATAGACTTG[A/C]TGGAGACAGGGTTGC	4799
rs751400317	snp	A/G	1.64776e-05	0.00287028	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33366693	ACCGCCGGATCATCC[A/G]TGACTTGGCCCAAGT	4799
rs751410410	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33316105	AGGCTTCCATCACCT[A/G]TTGTGAATCCTGACC	4799
rs751442579	snp	A/G			downstream-variant-500B	NFX1	GRCh38.p7	9:33371630	GTATCTAGAAAATAT[A/G]TACACATCTTCCTCC	4799
rs751459030	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33331050	GGGCGCCTGTAGTCC[C/G]AGCTACTCGGGAGGC	4799
rs751485816	snp	C/T	1.65018e-05	0.00287239	utr-variant-5-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33290560	CAGCTCGATCTAGGT[C/T]CTGCGGCACGGGATG	4799
rs751520416	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33327804	CTTGTCCTAAACCTA[C/G]TTTAGCAGCATGGAT	4799
rs751530598	snp	A/G	1.80755e-05	0.00300623	intron-variant	NFX1	GRCh38.p7	9:33295456	GATAGGAAATATTTT[A/G]TTGTCTTTTTAATTT	4799
rs751537368	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33342393	TGTGAACCTGGGAGG[C/T]GGAACTTGCAGTGAG	4799
rs751559126	snp	A/G/T	1.65745e-05	0.00287871	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294747	AGCACCATATCAGAG[A/G/T]CAAGAAAGCACAGAG	4799
rs751574564	snp	C/T	1.7828e-05	0.00298558	missense, nc-transcript-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33351777	CCTGCCCTGTGACTG[C/T]TTGTAAAGCTAAGGT	4799
rs751599342	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33323872	TCAAATAGAGAATAT[A/T]GATAAAGAGATAGAA	4799
rs751628729	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33337440	GGAGGTCCTGGAATC[A/G]GTCCCCCATGGACTC	4799
rs751645209	snp	A/G	1.6501e-05	0.00287232	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33338535	TATGTGTGACAAGCG[A/G]TGTAACAAGAAACGG	4799
rs751656490	in-del	-/A			intron-variant	NFX1	GRCh38.p7	9:33326413	CAAGCCTCTGTCTTT[-/A]AAAAAAAAAAAAAAA	4799
rs751667686	in-del	-/TC			intron-variant	NFX1	GRCh38.p7	9:33342119	GACCCTGTCTCTGTC[-/TC]TCTCTCTCTCACACA	4799
rs751694407	snp	C/G	1.76139e-05	0.00296759	intron-variant	NFX1	GRCh38.p7	9:33332551	GGGTGAAAGTGTCGT[C/G]ACTCTGAATCTTGTT	4799
rs751702494	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33310610	CCTCATGTCAGCCTT[C/G]TTTTCACTGTTCCAT	4799
rs751738597	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33302277	CATTTCTACTCTTCT[A/G]GTTATTTTGAAATAT	4799
rs751760562	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33303711	TAAACTCTATCCTGG[C/T]ATCTTCCCTCTTTAT	4799
rs751787511	in-del	-/TA			intron-variant	NFX1	GRCh38.p7	9:33341463	CAAACTGTATCAGTG[-/TA]TATATATATACATAA	4799
rs751871486	snp	A/G	1.64822e-05	0.00287068	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33311151	CCCTGCCTTTATGAC[A/G]AAAACATGTGAATGT	4799
rs751936006	snp	C/T	5.16658e-05	0.00508234	intron-variant	NFX1	GRCh38.p7	9:33364143	CTTTCTTAATTGTGG[C/T]TTGTCAGGGTGTTTG	4799
rs751956101	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33360437	GAGCTTGGCACATAG[G/T]AGGTACTCAGTAAAT	4799
rs751965322	in-del	-/TTC	1.64743e-05	0.00287	intron-variant	NFX1	GRCh38.p7	9:33344040	CAAACTCAGAAAGGA[-/TTC]TTTTGTTTTACCTGC	4799
rs751986608	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33310721	ATTACTTTGCTTAGA[C/T]TCTGATCTTCTACAG	4799
rs751991037	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33297448	AATAATTACCTCTTG[C/T]TTTATAGTGAATTAT	4799
rs752009150	snp	C/G	4.94271e-05	0.00497102	intron-variant	NFX1	GRCh38.p7	9:33344212	CAACTTGTCTTCACA[C/G]TTCAGCCTGCTCACA	4799
rs752032040	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33364542	TTCTTATATTTTTCT[C/G]TTTTGTTCTTCCGTC	4799
rs752033156	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33334872	CTGTCCCACTTTTTA[C/T]AACTTTATGATGCAA	4799
rs752037717	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33324680	TGCCTGTAATCCCAG[C/T]ATTTTGGGAGGCTGA	4799
rs752097779	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33356512	ATTTTTAATGTTAAT[A/G]TTATCCAGTTTATTT	4799
rs752107545	snp	A/C	1.65343e-05	0.00287521	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33319122	CTCTGCCTTGTGGTT[A/C]CTTAGGTAACTAGTA	4799
rs752112486	snp	A/G			utr-variant-3-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33371075	GCCCTAGAGCAAGCC[A/G]TGAGCCCCAGAGCAG	4799
rs752121359	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33293278	ATGTAAAGTGCTTAG[C/G]ATAGTGCCTGGCACA	4799
rs752139108	snp	C/G			intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352245	AGCCTTGTGGAGGGG[C/G]CTATGAGAGCAGGTA	4799
rs752178838	snp	C/G	1.65792e-05	0.00287912	intron-variant	NFX1	GRCh38.p7	9:33367651	GCTTTCCAAGGGGAC[C/G]TGTCTGTCCAGAAAA	4799
rs752191290	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33366976	CGACCCACAGGGCAG[A/G]TGCACTCAAAATGCA	4799
rs752195519	snp	A/T	1.64817e-05	0.00287064	intron-variant	NFX1	GRCh38.p7	9:33303164	TGGAAGAAAATTTAT[A/T]TGGCCTACTCCCATT	4799
rs752256678	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33333034	TATTTTTGGTAGAGA[C/T]GGGGTTTCACTGTGT	4799
rs752285099	snp	C/T			intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33365480	AGGTGTGGTGGTGCA[C/T]ACCCATAATCCCAGC	4799
rs752312227	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33290767	CGTACGAAGATCTGT[A/G]TCTTCTTGGACTAGA	4799
rs752313027	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33305052	TGACTTTGCCCCACA[C/T]TGTTCTTCCAGGGGA	4799
rs752313092	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33320442	TGATGCCCCATACCA[A/G]TGAGCAGTTTGAATT	4799
rs752331742	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33319597	TCACTGCAGCCTCTG[A/C]CTCCTGGGCTCAAAT	4799
rs752350712	snp	A/G	3.51339e-05	0.00419115	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33354178	CCAAAAAGGAAGTTC[A/G]TCAAGCCAGGTAATT	4799
rs752376581	snp	C/T	0.000131896	0.00811976	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294618	AGCATAGTTATCATC[C/T]GTCAGGAAGCAAACC	4799
rs752402702	snp	A/G	1.78512e-05	0.00298752	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33342784	GATTTGTGGGAGGAA[A/G]CTCCGTTGTGGCCTT	4799
rs752419688	snp	C/T			intron-variant, downstream-variant-500B	NFX1, LOC105376018	GRCh38.p7	9:33348941	ACGTATTGGCCAACA[C/T]TTCATGAAACTCTTG	4799
rs752427499	snp	C/T	1.64795e-05	0.00287045	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294548	AATTACAGTTCACCA[C/T]CTCCCTGTCACCTTT	4799
rs752440787	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33364401	GGAGGATCTCTGGGC[G/T]TCATTCCACTTCTGT	4799
rs752487982	snp	A/G	1.6473e-05	0.00286988	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33344090	ATGAATTAACCTGCC[A/G]TTGTGGTGCATCAGT	4799
rs752496378	snp	G/T	2.9773e-05	0.00385819	intron-variant	NFX1	GRCh38.p7	9:33342881	TACTGTATAGTTTAT[G/T]AGAAGAGTTTTTTAG	4799
rs752567124	snp	A/G	3.2956e-05	0.00405918	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33295329	CCAGGAGGGTTGACC[A/G]AGAGAAATGCACTGT	4799
rs752633056	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33293435	ATTTTAACCATTTTG[C/T]GTGTGTTATTAACTT	4799
rs752656128	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33339557	CCTCCCAAATTTCAT[A/G]TCCTCACATTTCAAA	4799
rs752676329	snp	A/G	3.29462e-05	0.00405857	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33318742	CAAGTATGCTATTGC[A/G]GCAGCACCTCCCGAG	4799
rs752685066	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33305979	CAGAACACTTGCAGG[A/G]GAAAGAAAAGCAAAA	4799
rs752706744	snp	C/T			intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33353396	CAGGGATCTGAGTGC[C/T]GAGATGGAGGTGTTA	4799
rs752724803	snp	C/G	1.64792e-05	0.00287042	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33295203	AGGGCCACCGACATA[C/G]AAACGCAGGACACAG	4799
rs752750039	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33328765	AATCAAAATAACCTC[A/G]GTAGATTAGGTATGG	4799
rs752752218	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33357122	CGAGACCATCCTGGT[A/G]AAACCCCATCTCTAC	4799
rs752785345	snp	C/T	1.71079e-05	0.00292466	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33351748	GTGTATGGCACCCTG[C/T]CATACCAGCTCACCC	4799
rs752811815	snp	C/T	1.64768e-05	0.00287021	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33366683	AACAGAGACCACCGC[C/T]GGATCATCCATGACT	4799
rs752836665	snp	C/G/T	3.33146e-05	0.00408122	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33351718	CACCACCCCCAGAGC[C/G/T]GACTGTGGTCACCCG	4799
rs752937678	in-del	-/AGAA			intron-variant	NFX1	GRCh38.p7	9:33300574	GCTGTATTGAAATCT[-/AGAA]AGACTTTGCTGCAAT	4799
rs752946352	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33329038	ATAAAAGGACTCACC[A/G]AACTTGCTGGTGGTT	4799
rs752962173	snp	A/G	1.65597e-05	0.00287743	intron-variant	NFX1	GRCh38.p7	9:33307337	TTGGGATTGCTGGTG[A/G]ACATGCTTTGCTGGT	4799
rs752963245	in-del	-/TTG	1.8275e-05	0.00302278	intron-variant	NFX1	GRCh38.p7	9:33301240	TTGAGTTAATCTTTT[-/TTG]TTATTTTGTTTTTTA	4799
rs752987048	snp	A/G	1.82703e-05	0.00302239	utr-variant-3-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33370007	CACTTAGATAAAAGA[A/G]TGATTAGGTATAGTG	4799
rs753004239	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33360508	TTTCTCCTCAATCTT[A/G]GTGATGACATAATGA	4799
rs753005658	snp	C/T	1.65806e-05	0.00287924	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33294778	TCTTGCTGAGCAGAC[C/T]TCAGATACAGCTGGA	4799
rs753015194	snp	A/T	8.54328e-05	0.00653522	intron-variant	NFX1	GRCh38.p7	9:33332528	GGTGGGGCATGAGGG[A/T]ATTTCTGGGGTGAAA	4799
rs753018462	in-del	-/CAGATTCCATTC	1.71991e-05	0.00293245	intron-variant	NFX1	GRCh38.p7	9:33338614	CTTATTAGGCATAAT[-/CAGATTCCATTC]ATCCAGGTGCTGGGC	4799
rs753076324	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33337045	AGGCGGAGGTTGCAG[C/T]GAGCAAATTTTTGTA	4799
rs753127976	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33309086	ATCCTGGCTGGGCGC[G/T]GTGGCTCATGCCTGT	4799
rs753162476	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33339638	TTAACGCAAAAGTCT[A/G]CAGTCCAAAGTCTCA	4799
rs753168068	snp	A/G			intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33365078	CAGGAGTTCTAGATC[A/G]GCTTGGCCAACATGA	4799
rs753192767	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33368282	CAAGTGGGTGTGGGG[A/G]TGAGAATTGCCGGTG	4799
rs753209207	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33309658	ACAGAGACAGGGTCT[C/T]GCTCTGTTGCCCAGG	4799
rs753242213	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33369484	CCATGTGCCCATTAC[A/C]AAATTTCAAAATCAC	4799
rs753295941	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33363882	GTTATTCTCTCCTTA[A/G]TAATCCAGTTTACCA	4799
rs753346973	snp	A/G	1.64746e-05	0.00287002	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33319036	TCTCAGCCAATTGCT[A/G]GAACTTGGAAGTAGT	4799
rs753361898	in-del	-/A	0.0513736	0.151814	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33364823	AAGGCCAGCTTGATG[-/A]AAAAAAAAAAAGCAA	4799
rs753384426	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33367985	ACGCCTGTAATCCCA[A/G]CACTTTGGGAGGCCA	4799
rs753391467	snp	C/T	0.000373065	0.0136526	intron-variant	NFX1	GRCh38.p7	9:33347660	ATTTACCGTTTGATC[C/T]AGCAGTCCCACTACT	4799
rs753459524	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33332056	AGCCGTTTGTCCCTG[C/T]ATTAAATGGTACAGA	4799
rs753502192	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33293966	CGTGATATCCCTAAG[C/T]TCATACAATAAGTTG	4799
rs753512511	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33344989	CAACATGGTGAAACC[A/G]TGTCTCTACTAAAAA	4799
rs753553235	snp	A/T	1.64765e-05	0.00287019	missense, nc-transcript-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352664	GAGCTACAGTGTGAA[A/T]GTGGACGAAGAAAAG	4799
rs753581917	snp	A/C	1.64735e-05	0.00286993	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33301364	TGTCAGAGCTGTTAC[A/C]ATGTGTTTCATTTGA	4799
rs753589325	snp	A/G	2.09426e-05	0.00323587	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33342751	CTTTTCCCAGGATAA[A/G]GAGCACAAGTGTCCT	4799
rs753616198	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33305790	GTGGGGACAGTGACT[A/G]CAGTTTAGAAATGTT	4799
rs753642287	snp	A/G	1.65504e-05	0.00287662	intron-variant	NFX1	GRCh38.p7	9:33354035	CCCAAGTATAAGGAG[A/G]TTCTTGTGAAACTGC	4799
rs753648254	snp	G/T			downstream-variant-500B	NFX1	GRCh38.p7	9:33371492	ACTTCAGATTCTAGC[G/T]GTGCCACATAATTTG	4799
rs753673717	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33292448	TTAGTCTGCCTTTCC[C/G]ACCTGTTGGACACCT	4799
rs753713076	snp	A/T	1.65064e-05	0.00287279	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33313787	TGCCAGATCATTTTG[A/T]ACCAGGGTAAGTGGT	4799
rs753753224	snp	A/G			intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33349612	AGCCTTTGGTCCTAC[A/G]AGAGTAAAATTTCAG	4799
rs753807128	snp	A/T	9.90769e-05	0.00703766	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33295057	TGACTCTTCAGAGGC[A/T]TCCTCTAGAAAAGGA	4799
rs753811440	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33337838	TGAATCACCTGAGGT[C/G]AGGTGTTCAAGACCA	4799
rs753889264	snp	C/T	1.64914e-05	0.00287149	intron-variant	NFX1	GRCh38.p7	9:33347032	GTTACCTTTCTCTTT[C/T]TGCAGTATATCATTC	4799
rs753944671	in-del	-/A			intron-variant	NFX1	GRCh38.p7	9:33338050	GAGACCCTGTCTCAG[-/A]AAAAAAAAAAAGAAA	4799
rs753947560	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33357942	TTAACTTGTAGGTCA[A/G]TTTGGAATCTTTACA	4799
rs753959250	in-del	-/T	1.65222e-05	0.00287417	frameshift-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33294949	GGACCAAAAGTCAAG[-/T]GGGAAACTCAAATGT	4799
rs754036140	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33299283	ACCCAATCCAGGATA[A/C]CACGTTGCATTTAGT	4799
rs754042118	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33325937	AACTGATTTAAAAAA[C/T]AACTGTATAAAATAA	4799
rs754086250	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33359175	TTATTGTCAATTCCT[A/G]TTATTTTTTTCCTTT	4799
rs754112867	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33355589	CATTATACTGTTAAT[A/G]GATATCTTTGTATTA	4799
rs754160309	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33367372	GGTTAAATGCAGGTG[A/G]CCATGTCTGAGAGCA	4799
rs754180653	snp	A/T	1.75937e-05	0.0029659	utr-variant-3-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33369984	CCAGGACTAAGAAGA[A/T]CATGATGCACTTAGA	4799
rs754204936	snp	A/C	1.93336e-05	0.00310909	intron-variant	NFX1	GRCh38.p7	9:33369871	CTGTTTCCCCCAAAG[A/C]AGAAAAGACTGATCA	4799
rs754231208	snp	A/C	1.64751e-05	0.00287007	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33328604	CATACCTGTGAAAAG[A/C]TCTGCCATGAAGGAG	4799
rs754232201	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33311575	TTTTTTTTTTTGAGA[C/T]GGAGTCTCGGTCTGT	4799
rs754279851	in-del	-/TC			intron-variant	NFX1	GRCh38.p7	9:33343148	TGTCCTCAACAATCT[-/TC]TTTCTCTATATTATT	4799
rs754290710	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33313579	TGAGGGGAGAGTTAG[A/G]GGCCGCAGTGTTAGT	4799
rs754312792	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33334892	TTATGATGCAAAATT[G/T]CAACCATACGTGAAA	4799
rs754325951	snp	A/C			intron-variant, utr-variant-3-prime, downstream-variant-500B	NFX1, LOC105376018	GRCh38.p7	9:33348322	GCACCACTGCACTCC[A/C]GCCTGGGCAACAGAG	4799
rs754326928	snp	A/G	1.65754e-05	0.00287879	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33294754	TATCAGAGTCAAGAA[A/G]GCACAGAGTCTTGCT	4799
rs754367663	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33340731	TGCTTCGCTACTTAG[A/C]AATTTCTTCCACCAG	4799
rs754367696	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33333255	AGGTCTTACTGTAGT[C/T]AGAAAGAAAGCTGTA	4799
rs754378328	snp	C/T	1.65269e-05	0.00287457	intron-variant	NFX1	GRCh38.p7	9:33307319	GTTGGAATGCTAATT[C/T]CGTTGGGATTGCTGG	4799
rs754380285	snp	C/T	4.9534e-05	0.0049764	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294650	AAGAGTCAGCAGACG[C/T]CTTTCCAGTCCTCTC	4799
rs754383221	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33358860	TACCACACCCAGCTA[A/G]TTTTTTTGTTTTTTT	4799
rs754455559	snp	G/T			intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33351100	AGTGAGCCCCGAGAT[G/T]GGCGCCACTGTACTC	4799
rs754472586	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33303915	TTACTGTCTGTCTCC[C/T]TCCCTGAAGCATTGC	4799
rs754474266	in-del	-/AA	0.0277946	0.114563	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33364824	AAGGCCAGCTTGATG[-/AA]AAAAAAAAAGCAATC	4799
rs754481079	snp	C/G	1.64743e-05	0.00287	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33319037	CTCAGCCAATTGCTA[C/G]AACTTGGAAGTAGTA	4799
rs754499988	snp	G/T	0.000876355	0.0209166	intron-variant	NFX1	GRCh38.p7	9:33319141	AGGTAACTAGTAAGC[G/T]TAAAGTTGGCTTTAA	4799
rs754512598	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33363891	TCCTTAATAATCCAG[C/T]TTACCAAAATAGAGA	4799
rs754516773	snp	G/T	1.64749e-05	0.00287005	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33301377	ACCATGTGTTTCATT[G/T]GAACTGCATAAAGAA	4799
rs754574697	snp	A/T	2.96441e-05	0.00384983	intron-variant	NFX1	GRCh38.p7	9:33354042	ATAAGGAGGTTCTTG[A/T]GAAACTGCAATGCCT	4799
rs754581703	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33317348	TGCTTGAGCCCGGGA[A/G]TTTGAGGCTGCAGTG	4799
rs754626165	snp	C/T	6.59044e-05	0.00574002	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352666	GCTACAGTGTGAATG[C/T]GGACGAAGAAAAGAG	4799
rs754656061	snp	C/T	1.6473e-05	0.00286988	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33367544	GTCCTCCTACCACGC[C/T]GACAGGTGTGCTTGA	4799
rs754675248	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33297409	TGTTATACCAGAGTT[G/T]TTACTGAATCCTTAA	4799
rs754688509	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33345674	TTTTTCCCACTCTTA[C/T]TATTATATTTTTGAT	4799
rs754723298	snp	C/T	1.83058e-05	0.00302532	intron-variant	NFX1	GRCh38.p7	9:33294412	CATGTCTATTTTTTA[C/T]GTCCTAGGTACTTTT	4799
rs754747689	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33330961	AGGTGGGCGGATCAT[A/G]AGGTCAGGAGATTGA	4799
rs754754194	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33325993	TATAACCTGTAGAAG[G/T]ATATTTGATAATTAT	4799
rs754802102	snp	A/G	1.651e-05	0.0028731	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33295065	CAGAGGCATCCTCTA[A/G]AAAAGGAGTATTGGA	4799
rs754807658	snp	A/G	2.04731e-05	0.0031994	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33342753	TTTCCCAGGATAAGG[A/G]GCACAAGTGTCCTTT	4799
rs754831254	snp	C/T	1.64806e-05	0.00287054	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294543	GAAGAAATTACAGTT[C/T]ACCACCTCCCTGTCA	4799
rs754865750	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33292456	CCTTTCCCACCTGTT[A/G]GACACCTACTGTGCT	4799
rs754893922	snp	A/G			missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33301387	TCATTTGAACTGCAT[A/G]AAGAAATGGGCAAGG	4799
rs754911870	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33298228	CCTCTTTGATAAGGA[A/G]ACATTTGAACAGAGA	4799
rs754929752	snp	A/C/T			intron-variant	NFX1	GRCh38.p7	9:33337917	AGCCGGGCGTGGTGG[A/C/T]GCACACCTGTAATCC	4799
rs754958644	in-del	-/G	3.9045e-05	0.00441825	intron-variant	NFX1	GRCh38.p7	9:33301213	ATTAAAGTGAGGAAT[-/G]GTTTTTTGTGTTTGA	4799
rs754968530	snp	A/C			intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352051	TCTCAATAGTCACTG[A/C]TTGTTTACTCCATTT	4799
rs754975530	snp	A/G	2.6403e-05	0.00363329	intron-variant	NFX1	GRCh38.p7	9:33364662	GTGAAAGGGGTTCTC[A/G]GAAGGGCAGGGACAG	4799
rs754992267	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33291596	AAAATGTATTTATTA[C/G]TATGGTTCTTAGTTT	4799
rs755008312	snp	C/T	1.7221e-05	0.00293432	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33364783	GAATAAGGTTGAAGT[C/T]GAAACATCCCACTGG	4799
rs755029734	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33333326	AAAAAGTGACTTTTA[C/T]GATAAGGGTGTTTAC	4799
rs755040825	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33300813	GCCATCTCACCACTC[A/C]TGGGTTGTTGGAACC	4799
rs755044520	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33347278	AATTTGCATACAACA[C/G]AATTTACCCTTTTTA	4799
rs755061500	snp	C/G	1.65307e-05	0.0028749	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33366605	AATGATATGATCAAT[C/G]AGTCATCTTTTCCCT	4799
rs755080345	snp	A/G	1.70093e-05	0.00291622	intron-variant	NFX1	GRCh38.p7	9:33319146	ACTAGTAAGCGTAAA[A/G]TTGGCTTTAAAAATA	4799
rs755087550	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33359303	ATGGAGGGTGGTAAT[A/T]ATAGATATTCCTTGG	4799
rs755097574	snp	A/G/T	3.29496e-05	0.00405881	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33328611	GTGAAAAGCTCTGCC[A/G/T]TGAAGGAGACTGTGG	4799
rs755131177	snp	A/G	1.64844e-05	0.00287087	missense, nc-transcript-variant	NFX1, LOC105376018	GRCh38.p7	9:33351591	CCTGTCACCTGGTTG[A/G]TATCTCTTGCGGATT	4799
rs755133879	snp	C/T	8.23676e-05	0.00641693	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33303236	GTCAGAATGTTTCTG[C/T]ACATGTTCCTAATAC	4799
rs755142469	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33314181	TAGAGATAGGGTTTC[A/T]CAATGTTGGCCAGGC	4799
rs755171961	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33345785	TATTCAGTCAGTCTT[A/G]TGTTGCTGGACATTT	4799
rs755189763	snp	A/G	1.86308e-05	0.00305206	intron-variant	NFX1	GRCh38.p7	9:33369886	AAGAAAAGACTGATC[A/G]TTCTTTGTTTGTTTT	4799
rs755235263	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33299359	TCCTTTTTGGAAAAG[A/T]TGTTTCTGCTCTTGT	4799
rs755255485	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33308197	CTATAATCCCAACAC[A/G]TTGGGAAGCCAAGGC	4799
rs755292345	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33313030	TAATGCCATTGTGCT[A/G]TTAGTCTGAGTGTGT	4799
rs755311472	snp	C/G	1.65149e-05	0.00287353	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294655	TCAGCAGACGTCTTT[C/G]CAGTCCTCTCCTTGT	4799
rs755315460	snp	A/G	1.78535e-05	0.00298771	utr-variant-3-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33369991	TAAGAAGATCATGAT[A/G]CACTTAGATAAAAGA	4799
rs755328581	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33368190	CAGTGAGCCGAGATC[A/G]CACCACTGCACTCCA	4799
rs755341463	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33305583	GGTAGCAGTGAGTAG[A/G]GTATTTTGGAGCCTA	4799
rs755343225	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33336930	AACAAGGTGAAACCC[C/T]GTCTCTACTAAAAAT	4799
rs755351291	snp	C/T	3.79571e-05	0.00435627	intron-variant	NFX1	GRCh38.p7	9:33354203	GTAATTTTTAAAATG[C/T]ATATATGTGCCTTCT	4799
rs755352739	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33322480	CATTTCTCTACCCCT[A/C]CAACTCCAAGTTGAA	4799
rs755362923	snp	C/T	4.96537e-05	0.00498241	intron-variant	NFX1	GRCh38.p7	9:33307171	AGTTTGTACCATTGA[C/T]TCTCTGATCTGATAT	4799
rs755415074	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33353993	CCACACCTGGCCTAG[A/G]TTTGCTTTTAAAGAG	4799
rs755531408	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33330732	TGTCCTCACTCCCTC[C/T]AATAGTGGACTCCAT	4799
rs755546276	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33334937	ATAATGAATCCCCAC[G/T]TACCTATGACCTGTC	4799
rs755548405	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33320898	AGTGGGAACACCCTA[C/G]TTAATCCTTTTTCTC	4799
rs755564182	snp	A/G	1.64841e-05	0.00287085	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33295369	GGATCCTCAAGTAGT[A/G]TCTCCTTTCTCCCGA	4799
rs755582830	snp	A/C			intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33365197	GAGAATTCCTTGAAC[A/C]CGGGAGGCAGAGGTT	4799
rs755605902	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33316391	TCCCAAGTAGCTGGC[A/G]CTACAGATGCACACC	4799
rs755616380	in-del	-/TG			intron-variant	NFX1	GRCh38.p7	9:33333045	GAGACGGGGTTTCAC[-/TG]TGTTGGCCAGGCTGG	4799
rs755634970	in-del	-/TG			intron-variant	NFX1	GRCh38.p7	9:33310378	GTATTTCTGTACCAC[-/TG]TGTAATTTGCCAAAG	4799
rs755666826	in-del	-/GAG	1.64806e-05	0.00287054	cds-indel, nc-transcript-variant	NFX1	GRCh38.p7	9:33347058	CATTCTTGTCATAGT[-/GAG]GAGAAGTGTCCCCCT	4799
rs755720948	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33290819	TTTCGGAGGAGAGAG[A/G]ACTTGTCCCGGCGCT	4799
rs755723817	snp	A/G	3.29451e-05	0.00405851	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33318775	GTGTTATGTGGAACC[A/G]ATGTAGGAAAGTCTG	4799
rs755724429	snp	C/T	3.92141e-05	0.00442781	intron-variant	NFX1	GRCh38.p7	9:33301215	TAAAGTGAGGAATGG[C/T]TTTTTGTGTTTGAGT	4799
rs755754909	snp	G/T	1.64841e-05	0.00287085	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33366714	TGGCCCAAGTTTATG[G/T]CCTGGAGAGCGTGAG	4799
rs755768124	snp	A/G	4.95086e-05	0.00497512	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33295080	GAAAAGGAGTATTGG[A/G]TGGGTATGGAGCCAG	4799
rs755808061	snp	C/T	1.70487e-05	0.0029196	intron-variant	NFX1	GRCh38.p7	9:33366786	TCAGGTAGGTCAATC[C/T]CGCCGTCAGAGGAAG	4799
rs755836467	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33291425	ATATGTCACAGCCCA[C/T]TGCCTTCATTTGATT	4799
rs755837540	snp	C/G	1.84164e-05	0.00303444	intron-variant	NFX1	GRCh38.p7	9:33294388	GATGAAGTTTAATCT[C/G]TTTACTGGCATGTCT	4799
rs755841040	snp	A/C/G			intron-variant	NFX1	GRCh38.p7	9:33308905	TGGGGAAATGTCAGT[A/C/G]GGGGTAGAGCTGTTT	4799
rs755846664	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33319699	ATTTTTAATAGAGAC[A/G]GGGTTTCACCATGTT	4799
rs755853956	snp	A/G	1.66037e-05	0.00288125	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33338561	AACGGTTGTGTGGAC[A/G]GCATAAATGTAATGA	4799
rs755948726	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33324056	AGACCAGCCTGAGCA[C/T]GTAGTGAGACCCTAT	4799
rs755949287	snp	C/T	1.64819e-05	0.00287066	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352629	CTAAAAGTCGTTCCA[C/T]GTTCATCTGACTTCA	4799
rs755962219	snp	A/G	1.65081e-05	0.00287293	utr-variant-5-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33290570	TAGGTTCTGCGGCAC[A/G]GGATGGCGGAGGCGC	4799
rs755980130	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33363786	TAAGTCCCCAGTGTT[C/T]AGCCTATGACTTGCT	4799
rs755980358	snp	C/T	2.6164e-05	0.00361681	intron-variant	NFX1	GRCh38.p7	9:33338479	ATATCCTTTGTCTGG[C/T]TTTTTTTTTCTTTTT	4799
rs756035252	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33303792	GAAAACTTCTTGTAA[C/T]CCAGATGCTCATTCT	4799
rs756053827	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33304540	CTCTGAATCTTCTAG[A/G]TGCAATACCTTGGTG	4799
rs756181743	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33357786	TCTGGCTCAAGCGAA[A/C]CTCCTGCCTTGGCCC	4799
rs756184485	snp	A/G	0.000473597	0.015381	intron-variant, utr-variant-3-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33347755	GCAGCACAATTCACA[A/G]TTGCAAAAATGTGGA	4799
rs756226064	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33312760	CCTGTAGCCCCAGCT[A/C]CTGGGGAGGTTGAGG	4799
rs756236900	snp	C/T	1.65059e-05	0.00287275	synonymous-codon, nc-transcript-variant	NFX1, LOC105376018	GRCh38.p7	9:33351568	CTCCTAGTTTCGGAG[C/T]AACATCCCCTGTCAC	4799
rs756238391	snp	G/T	1.65154e-05	0.00287358	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33295055	CCTGACTCTTCAGAG[G/T]CATCCTCTAGAAAAG	4799
rs756269481	snp	G/T	1.75529e-05	0.00296246	intron-variant	NFX1	GRCh38.p7	9:33364158	CTTGTCAGGGTGTTT[G/T]GTCTTTTGAGATGTC	4799
rs756279086	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33325710	AACCAAGAATCTTAC[A/G]TCTCATGAAACTAAC	4799
rs756279196	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33310869	TATAACCAGTATTTT[G/T]ACTTGGGATTTACTT	4799
rs756304158	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33356712	TTCAGCTTTTTTCCA[C/T]GTGAATATCCATTTG	4799
rs756330478	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33355471	ATTTTTGTCTGGCTT[C/G]TTTCGTTATATTTTT	4799
rs756469051	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33325024	GAAATGTGGGACACC[C/T]TTAACTGTATCAGTG	4799
rs756502240	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33319668	GCGCACACCACCACG[A/C]CCGGCTAATTTTTGT	4799
rs756509327	snp	C/G	1.68319e-05	0.00290098	intron-variant	NFX1	GRCh38.p7	9:33319140	TAGGTAACTAGTAAG[C/G]GTAAAGTTGGCTTTA	4799
rs756544379	snp	C/T	1.65743e-05	0.00287869	intron-variant	NFX1	GRCh38.p7	9:33307147	CATTAAAGTTGAGAA[C/T]GTGGTTGAAGTTTGT	4799
rs756547976	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33340528	GGAGACATTTTCCCC[A/G]TTGTCTTGGGGTTTT	4799
rs756577903	snp	C/G	1.64779e-05	0.00287031	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294572	CACCTTTCCAGGCAG[C/G]TCCCTTATGATGAAA	4799
rs756589650	snp	C/T			intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33365773	AAGGGCTATTGTATG[C/T]TAGGAAAGCCCACTG	4799
rs756642355	in-del	-/TGG	2.34321e-05	0.00342279	intron-variant	NFX1	GRCh38.p7	9:33364689	ACAGACAAAATTAAC[-/TGG]TGATTTCTCATTTCA	4799
rs756643018	snp	G/T	1.80703e-05	0.0030058	splice-donor-variant	NFX1	GRCh38.p7	9:33354189	GTTCATCAAGCCAGG[G/T]AATTTTTAAAATGCA	4799
rs756658119	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33337113	AATTCCTGGGCTCGA[A/G]CAATCCTCCTGCCCT	4799
rs756660168	in-del	-/TAT			intron-variant	NFX1	GRCh38.p7	9:33363275	ATGTATTATTATTAT[-/TAT]TATTATTATTATTAT	4799
rs756670990	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33332290	GGAGTCCTCTTGTGA[A/G]TAAAGCTCATTCATA	4799
rs756671203	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33346841	TCCTTGGTTGGGTTT[C/G]TTTTTCTCACTCATG	4799
rs756690663	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33299144	TCTAATGTTAACGTC[C/T]TACATAACCAGACTG	4799
rs756698809	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33342394	GTGAACCTGGGAGGC[A/G]GAACTTGCAGTGAGC	4799
rs756708991	snp	A/G	1.6486e-05	0.00287102	intron-variant	NFX1	GRCh38.p7	9:33318684	TGTGACATTTTAAGA[A/G]CCCATACATGTTACT	4799
rs756733794	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33327919	TTCAGAGTCGACAGC[A/G]TTCCACTAAAGTCAT	4799
rs756734017	in-del	-/G			intron-variant	NFX1	GRCh38.p7	9:33316449	CTCTTGATTCATATT[-/G]GGCTTTTACTCAGCT	4799
rs756757277	snp	A/C/G	1.65784e-05	0.00287905	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294798	ATACAGCTGGATTAG[A/C/G]GAGCTCGACCAGATC	4799
rs756761905	snp	A/T	4.23738e-05	0.00460273	intron-variant	NFX1	GRCh38.p7	9:33342903	GTTTTTTAGAAATTC[A/T]GACATAATATACTTT	4799
rs756781204	snp	G/T	1.6473e-05	0.00286988	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33344109	TGGTGCATCAGTGAT[G/T]TACCCTCCAGTTCCC	4799
rs756804844	in-del	-/A			intron-variant	NFX1	GRCh38.p7	9:33331174	TCTCAAAAAAAAAAT[-/A]AAAAAAAATAAGCTG	4799
rs756822193	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33341020	ACTGTTCCAACATCT[G/T]CCTGTTACCCAGTTC	4799
rs756871615	snp	C/T	1.83913e-05	0.00303238	intron-variant	NFX1	GRCh38.p7	9:33354844	TTTTTTTCATTTGCT[C/T]ATCAAGGCTGGAGTG	4799
rs756878970	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33368189	GCAGTGAGCCGAGAT[C/T]GCACCACTGCACTCC	4799
rs756951810	snp	A/T	3.29554e-05	0.00405914	stop-gained, nc-transcript-variant	NFX1	GRCh38.p7	9:33366699	GGATCATCCATGACT[A/T]GGCCCAAGTTTATGG	4799
rs756973325	snp	A/G	1.64893e-05	0.0028713	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33366641	CAGGGAAAGAATAGT[A/G]AGAAAAGCCACAGCT	4799
rs757001181	snp	A/G	1.81744e-05	0.00301444	missense, nc-transcript-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33351785	GTGACTGCTTGTAAA[A/G]CTAAGGTGGGTATTT	4799
rs757022239	snp	C/T	1.81939e-05	0.00301606	intron-variant	NFX1	GRCh38.p7	9:33295457	ATAGGAAATATTTTG[C/T]TGTCTTTTTAATTTA	4799
rs757030709	in-del	-/AAC			intron-variant	NFX1	GRCh38.p7	9:33324257	GCGGCACACGCCTGT[-/AAC]AATCCTGGCTATTTG	4799
rs757067103	snp	A/G	1.648e-05	0.0028705	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33295347	AGAAATGCACTGTAC[A/G]GAGGCAGGATCCTCA	4799
rs757083888	snp	C/T			intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33349812	CAGAAAACAGCCTCC[C/T]AGCCTGGGCAACCTA	4799
rs757083957	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33335162	CTTAGTTCTTTCACA[A/G]TCTAGTTCCAAAATA	4799
rs757108986	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33361483	CGGTACTTAAAATTA[G/T]AGAGAAAGGCTGGGC	4799
rs757127069	snp	A/T	1.67413e-05	0.00289316	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33351727	CAGAGCTGACTGTGG[A/T]CACCCGTGTATGGCA	4799
rs757205348	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33329252	GCCAGCATACATGGA[A/G]TATTGCCAACCAGGA	4799
rs757208353	snp	C/T	1.65364e-05	0.0028754	intron-variant	NFX1	GRCh38.p7	9:33338463	TGTTGTATGAATGTT[C/T]ATATCCTTTGTCTGG	4799
rs757233908	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33309240	TGGGCACCTGTAGTC[C/T]CACCTACTGGAGAGG	4799
rs757248956	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33314399	AAAAATGAACTGGCC[A/G]GGCATAGTGGCTCAT	4799
rs757253017	snp	A/G	1.65045e-05	0.00287263	utr-variant-5-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33290563	CTCGATCTAGGTTCT[A/G]CGGCACGGGATGGCG	4799
rs757287370	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33323913	AAAGAGGCCCAAATG[A/G]AAATTCTGAAGTTTA	4799
rs757309589	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33324736	ATCGAGACCATCCTG[A/G]CTAACATGGTGAAAC	4799
rs757339389	in-del	-/TA			intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33353426	GAGAATGAATGGTTA[-/TA]TATATATATATATCT	4799
rs757339907	snp	A/G	3.31559e-05	0.00407147	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294801	CAGCTGGATTAGAGA[A/G]CTCGACCAGATCAGA	4799
rs757354935	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33369697	TCACAGAATAAAATT[C/G]CCCATGTAATATGTA	4799
rs757392035	snp	A/C	1.64798e-05	0.00287047	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33311157	CTTTATGACAAAAAC[A/C]TGTGAATGTGGACGA	4799
rs757410034	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33368668	AAGCCCAGAAGGAGA[C/G]GGGTGCCTACTCCTG	4799
rs757445040	snp	A/G	1.65979e-05	0.00288074	intron-variant	NFX1	GRCh38.p7	9:33311056	GGGACAGCTTTGTTC[A/G]GGTTTGGATACATGG	4799
rs757447295	snp	A/G	1.65206e-05	0.00287403	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33338543	ACAAGCGGTGTAACA[A/G]GAAACGGTTGTGTGG	4799
rs757472551	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33331882	CCATCATCACTACAC[A/G]CGATTTTTAGGATCA	4799
rs757475507	snp	A/T	1.67119e-05	0.00289062	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33364027	GATTAGCAGAGGCAT[A/T]TCATATCAGTGAGGA	4799
rs757480133	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33329441	CCTGCTCCTAAATCA[C/T]GTAATTGGACTATCC	4799
rs757488500	snp	A/G	4.95692e-05	0.00497816	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33294961	CAAGGGGAAACTCAA[A/G]TGTGAATGGAGTAAC	4799
rs757534708	in-del	-/T			intron-variant	NFX1	GRCh38.p7	9:33357706	CTGGCTAAGATTTTC[-/T]TTTTTTTTTTTTTTT	4799
rs757546421	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33364442	CTCACATTCACATGC[A/G]TTCTCAGTTGGAGCT	4799
rs757548322	in-del	-/TTTTG	1.64741e-05	0.00286998	intron-variant	NFX1	GRCh38.p7	9:33344043	ACTCAGAAAGGATTC[-/TTTTG]TTTTACCTGCTGCTC	4799
rs757607292	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33336567	TGATATATCACTACC[A/G]CATGATGTGATGTCT	4799
rs757635929	in-del	-/TAT			intron-variant	NFX1	GRCh38.p7	9:33363264	AATAATAAAGAAATG[-/TAT]TATTATTATTATTAT	4799
rs757638469	snp	A/G	4.98475e-05	0.00499212	intron-variant	NFX1	GRCh38.p7	9:33319131	GTGGTTCCTTAGGTA[A/G]CTAGTAAGCGTAAAG	4799
rs757659652	snp	C/T	0.000257699	0.0113483	intron-variant, missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33347721	ATATGAAAAAGATAC[C/T]TGCACACGCATGTTT	4799
rs757669423	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33331198	TAAGCTGATAATTAT[C/G]ACCTCATTGTTTAAC	4799
rs757691772	snp	A/C/G	4.94257e-05	0.004971	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33301385	TTTCATTTGAACTGC[A/C/G]TAAAGAAATGGGCAA	4799
rs757698482	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33357775	GGTCTCAAACTTCTG[A/G]CTCAAGCGAACCTCC	4799
rs757751680	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33297499	TAACACACATTTACT[A/G]TGCCACTGTTTCTGT	4799
rs757785786	in-del	-/AAG	1.64811e-05	0.00287059	intron-variant	NFX1	GRCh38.p7	9:33311200	TAAAATTACACCCTA[-/AAG]AAGACCTCAGTTTTC	4799
rs757796283	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33311842	AGGCATGAGCTACCG[C/T]GCTCGGTCGGCAAGG	4799
rs757802820	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33296595	AAAAAATTAGCCAGG[C/G]ATGTTAGCACATGCC	4799
rs757827629	snp	C/T	1.65187e-05	0.00287386	intron-variant	NFX1	GRCh38.p7	9:33367467	CTTTCTGTCCATCTC[C/T]ACAAACAATTCTCAC	4799
rs757844634	snp	C/T	3.5517e-05	0.00421394	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33342788	TGTGGGAGGAAACTC[C/T]GTTGTGGCCTTCATA	4799
rs757851928	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33314460	GGCCGGTGGATCACT[C/T]GAGGTCAGCAGATTG	4799
rs757871082	snp	G/T	1.64819e-05	0.00287066	intron-variant	NFX1	GRCh38.p7	9:33303167	AAGAAAATTTATTTG[G/T]CCTACTCCCATTTTT	4799
rs757878976	snp	C/G	1.64732e-05	0.0028699	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33367562	CAGGTGTGCTTGAAA[C/G]GGAAATGCAGGCACG	4799
rs757895913	snp	A/T	3.25187e-05	0.00403216	intron-variant	NFX1	GRCh38.p7	9:33354057	TGAAACTGCAATGCC[A/T]CTTTTTCCCTTTCTT	4799
rs757922966	snp	A/T	1.76543e-05	0.002971	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33354179	CAAAAAGGAAGTTCA[A/T]CAAGCCAGGTAATTT	4799
rs757940215	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33306072	AAACCAGGGCACTGT[A/T]TTGGAGCAAAAAAGC	4799
rs757961704	snp	C/T			intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352420	AGCCAGGATTAAGAA[C/T]AGAGGTGGTTTCCAA	4799
rs757991037	snp	C/T	9.88419e-05	0.00702931	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33313688	CAGGCTGTCTCAGTC[C/T]ACTGTTCTAACCCAT	4799
rs757995287	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33320501	TGTTTATATTCTTAT[C/T]AGTGCTTTTAGTATG	4799
rs758131575	in-del	-/TA			intron-variant	NFX1	GRCh38.p7	9:33341462	CAAACTGTATCAGTG[-/TA]TATATATATATACAT	4799
rs758141714	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33368985	GAGGGGTTTTCTCAG[A/G]AACTGCCAGAGTCGG	4799
rs758142916	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33313187	CTTCATGGAACTCAG[A/G]GATGAAATCACATAA	4799
rs758162267	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33314302	TCTAATTTAAATAGT[A/G]GATTTTAAAATGCTG	4799
rs758191648	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33319604	AGCCTCTGACTCCTG[C/G]GCTCAAATGATTCTT	4799
rs758224012	snp	C/T	1.65968e-05	0.00288065	intron-variant	NFX1	GRCh38.p7	9:33313821	CACACCAGCTAGCAA[C/T]GCTTGTGTTCTTTTC	4799
rs758240529	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33347521	AAGAATGGCAATAAT[A/C]AAAAAATAATAGATG	4799
rs758240993	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33360522	TGGTGATGACATAAT[A/G]ACCCTTACTGGATAG	4799
rs758263494	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33294355	TTTAGATTTGGCTTG[A/G]AGTCTATGAGTTTCA	4799
rs758297806	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33359455	AATACAAAAATTAGC[C/T]GGGCATGGTGGCAGA	4799
rs758363726	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33322633	ACCCCAGCTCACTCG[A/T]AGGGCAGAGGTTCCA	4799
rs758398298	snp	G/T	1.64792e-05	0.00287042	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33295337	GTTGACCAAGAGAAA[G/T]GCACTGTACGGAGGC	4799
rs758415563	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33335037	AAGTACTTTGAAAAC[A/C]AATCTCAAATATCAT	4799
rs758438685	in-del	-/AG			intron-variant	NFX1	GRCh38.p7	9:33346182	ATACCAGCATGAAGT[-/AG]ACATGCCCAGGCCAG	4799
rs758448189	snp	C/T			missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33367582	ATGCAGGCACGGCCT[C/T]CACCACCGATTCCTC	4799
rs758458758	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33336490	AAGTGCTGGGATTAC[A/G]GGCGTGAGCCACCGC	4799
rs758485096	snp	C/T	1.65899e-05	0.00288005	intron-variant	NFX1	GRCh38.p7	9:33307343	TTGCTGGTGGACATG[C/T]TTTGCTGGTGGCTCT	4799
rs758495561	snp	C/G	1.65272e-05	0.0028746	intron-variant	NFX1	GRCh38.p7	9:33307180	CATTGACTCTCTGAT[C/G]TGATATGTTCTAGGC	4799
rs758507443	snp	A/C	1.67598e-05	0.00289476	intron-variant	NFX1	GRCh38.p7	9:33354927	TTTTTAATCTCCTTG[A/C]CCTTGAGCTCTGTGA	4799
rs758538041	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33302083	TCTCAAACAAACAAA[A/C]AAACATTTTTTTTTC	4799
rs758539930	snp	C/T	1.72252e-05	0.00293467	intron-variant	NFX1	GRCh38.p7	9:33332534	GCATGAGGGAATTTC[C/T]GGGGTGAAAGTGTCG	4799
rs758589543	snp	C/T	3.295e-05	0.00405881	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33328637	TGTGGACCATGCTCT[C/T]GCACATCAGTTATTT	4799
rs758591739	snp	C/G	1.72341e-05	0.00293543	missense, nc-transcript-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33351756	CACCCTGCCATACCA[C/G]CTCACCCTGCCCTGT	4799
rs758607590	snp	C/T	1.83893e-05	0.00303221	utr-variant-3-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33370011	TAGATAAAAGAATGA[C/T]TAGGTATAGTGGAGA	4799
rs758670510	snp	A/T			missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33344073	TGCTCCACCAGGTTT[A/T]GATGAATTAACCTGC	4799
rs758688253	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33301028	GGGAATGTTTCCTTA[A/G]TTGTGGGAATCCCCA	4799
rs758709335	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33356424	GCACTCTGTACCTTC[A/G]TTTTTTACTCTCTTG	4799
rs758715470	snp	G/T	1.6582e-05	0.00287936	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294782	GCTGAGCAGACCTCA[G/T]ATACAGCTGGATTAG	4799
rs758718536	in-del	-/GAAGA	1.78253e-05	0.00298535	frameshift-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33342809	GGCCTTCATAGGTGT[-/GAAGA]ACCTTGTCATCGTGG	4799
rs758723971	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33296409	CTGTCACTCAGTTCG[C/T]TGACGAAGTCTTACT	4799
rs758738066	snp	G/T	1.64735e-05	0.00286993	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33344161	TGTACCCAAACCTGC[G/T]CTAGAGTCCATGAGT	4799
rs758755334	snp	A/G			intron-variant, utr-variant-3-prime, downstream-variant-500B	NFX1, LOC105376018	GRCh38.p7	9:33348455	CTAAGGAACTTATCC[A/G]TGTAACCAAACACCA	4799
rs758761807	snp	A/G	4.95626e-05	0.00497784	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294951	GACCAAAAGTCAAGG[A/G]GAAACTCAAATGTGA	4799
rs758775263	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33309140	AGGCGGGTGGATCAC[A/G]AGGCCAGGAGATCGA	4799
rs758784376	snp	C/T	6.59467e-05	0.00574187	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33347038	TTTCTCTTTCTGCAG[C/T]ATATCATTCTTGTCA	4799
rs758845691	snp	A/T	5.0635e-05	0.0050314	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33364013	TCTCTCTTTCAGGAG[A/T]TTAGCAGAGGCATTT	4799
rs758875711	in-del	-/AATT	1.65068e-05	0.00287283	intron-variant	NFX1	GRCh38.p7	9:33301425	CATCTCAAGCAGGTC[-/AATT]AATTCTCTCTTCTGA	4799
rs758884575	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33355140	CATCACATAACACAG[C/T]ATACTTATTCAGGGA	4799
rs758944962	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33307610	AAAGCCAGTGCTGCT[A/T]CCATTACATTACACT	4799
rs758945869	snp	A/C			intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33365264	GGGCAACAAGAGTGA[A/C]ACTCTGTCTCAAAAA	4799
rs758948084	snp	G/T	1.65012e-05	0.00287234	missense, nc-transcript-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33351671	TGTCACAAAGGGGAG[G/T]GTCTTGTGGATGAGC	4799
rs758991948	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33299871	CTCTATTTCTTTTGA[C/T]ATTAAACTGAACAAT	4799
rs759008909	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33323717	GCGATTGCGCCACTG[C/T]ACTACAGCCTGGGCA	4799
rs759065043	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33332959	CAAGTGATTCCCCTG[C/T]CTCAGCCTCCCAAGT	4799
rs759090798	snp	C/T	1.64925e-05	0.00287158	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33295134	CACAGAAAAGGCCTC[C/T]CTGGGAAGTGGAGGG	4799
rs759119173	snp	A/G	1.69559e-05	0.00291164	intron-variant, nc-transcript-variant	NFX1, LOC105376018	GRCh38.p7	9:33351533	CCCACATGGAGATGA[A/G]AATCTGGCTACTTCT	4799
rs759134301	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33332060	GTTTGTCCCTGCATT[A/G]AATGGTACAGATTGT	4799
rs759165372	snp	C/G			intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33350563	TCACATTTTTGGCTT[C/G]TGCTGCAAATCCTTT	4799
rs759178801	snp	A/C	3.31774e-05	0.00407279	intron-variant	NFX1	GRCh38.p7	9:33328544	GAAAATGAGTAGTTG[A/C]AGTTTTCATTTCCAG	4799
rs759182807	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33358742	ATTACAGCTCACTGC[A/G]GCCTCTACCTCCTGG	4799
rs759234987	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33312517	ACTCTTCTTGCAGGA[A/G]AGTAGACTCCAAGTG	4799
rs759256266	snp	C/T			intron-variant, utr-variant-3-prime	NFX1	GRCh38.p7	9:33348265	GCTGAGGCAGGAGAA[C/T]TGCTTGAACTCGGGA	4799
rs759309570	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33293202	TGTGGCCTTGGGCAA[A/G]TTCCTACTCTCTGTG	4799
rs759312653	snp	C/T	2.398e-05	0.00346257	intron-variant	NFX1	GRCh38.p7	9:33342866	GCCAGTGAGTGTCTT[C/T]ACTGTATAGTTTATT	4799
rs759362441	snp	C/T	1.64852e-05	0.00287094	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33294613	TCATCAGCATAGTTA[C/T]CATCCGTCAGGAAGC	4799
rs759366147	snp	A/G	3.43159e-05	0.00414207	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33354151	GTTCAGTGGAGATCA[A/G]CAAGTTAATTACCAA	4799
rs759378010	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33303913	CTTTACTGTCTGTCT[C/G]CCTCCCTGAAGCATT	4799
rs759385173	in-del	-/C			intron-variant	NFX1	GRCh38.p7	9:33347285	ATACAACAGAATTTA[-/C]CCTTTTTATTGTACA	4799
rs759402860	snp	A/T	1.6473e-05	0.00286988	stop-gained, nc-transcript-variant	NFX1	GRCh38.p7	9:33344081	CAGGTTTTGATGAAT[A/T]AACCTGCCATTGTGG	4799
rs759421646	snp	A/C/G	3.29605e-05	0.00405948	intron-variant	NFX1	GRCh38.p7	9:33303293	TTTATATACACTGGA[A/C/G]TCTCTTTTACTACAT	4799
rs759436885	in-del	-/A			intron-variant	NFX1	GRCh38.p7	9:33308730	TATGCGGCTCGATAT[-/A]AGAGTCTTTCTGGCA	4799
rs759532222	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33321386	AACAATGACTGTCAG[A/G]TTTGTTCAGACCTAG	4799
rs759581812	snp	C/G	1.67142e-05	0.00289081	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33366769	TGTGGTGGTCACTGC[C/G]ATCAGGTAGGTCAAT	4799
rs759584759	snp	A/G	3.29468e-05	0.00405861	intron-variant	NFX1	GRCh38.p7	9:33318874	CTAAAGCTGCACTTT[A/G]TGCAACAATTATGTA	4799
rs759585226	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33320282	ATGAATATTTTTCTA[A/C]AATTTACATTTCATG	4799
rs759595677	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33315550	AGGCCTAACAGCTGT[A/G]ATTGCTTCATTTCTT	4799
rs759597425	snp	C/T	1.65529e-05	0.00287683	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33294709	CCTTCAGAATCAACC[C/T]TGGCAGAAATTGAGG	4799
rs759654671	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33360849	TGGAAATCTAGCAGT[A/G]TGAACCAGATTCTTG	4799
rs759663752	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33342223	CCCCAGCACTTTGGG[A/G]GGCCAAGGTGGGCGG	4799
rs759695372	snp	C/T	3.29549e-05	0.00405911	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33366680	ATGAACAGAGACCAC[C/T]GCCGGATCATCCATG	4799
rs759746513	snp	C/G	0.000288358	0.012004	missense, nc-transcript-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33351740	GGTCACCCGTGTATG[C/G]CACCCTGCCATACCA	4799
rs759775410	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33295586	GTTCTACCACCACTC[G/T]CTGCTCCCTGCCCCA	4799
rs759775529	in-del	CTCTGTTACCCAGG/TT			intron-variant	NFX1	GRCh38.p7	9:33302394	TGAGACAGAGTCTTA[CTCTGTTACCCAGG/TT]CTGGAGTCCAGTGGT	4799
rs759796113	snp	A/G	1.6483e-05	0.00287076	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33338515	GCCACAGCAGATGCT[A/G]CATTTATGTGTGACA	4799
rs759849666	snp	A/G	0.000135713	0.00823638	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352453	GGGGGCATTGTGGAC[A/G]GGGCAATTCTTTCCT	4799
rs759854404	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33323646	TGGTCCCAGCTGCTC[C/T]GGCGGCTGAGGCAGG	4799
rs759863066	snp	A/G	1.66241e-05	0.00288302	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33295426	TGTGGAAACGCACAC[A/G]GGTAAACCTACCTAG	4799
rs759896209	snp	A/G	4.96192e-05	0.00498067	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33366745	CTATGACAGTGAACC[A/G]AAGCGCAATGTGGTG	4799
rs759897813	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33367268	GATCACTCTCAGAAC[C/T]TGGGAATAGGAAGAA	4799
rs759908015	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33337044	GAGGCGGAGGTTGCA[A/G]TGAGCAAATTTTTGT	4799
rs759909124	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33363992	CCTTTTATTTGCATA[C/T]CTCTCTCTCTCTTTC	4799
rs759946910	snp	C/T	1.64991e-05	0.00287215	utr-variant-5-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33290550	CTTGGCTGTACAGCT[C/T]GATCTAGGTTCTGCG	4799
rs759975588	snp	C/G	4.86772e-05	0.00493318	intron-variant	NFX1	GRCh38.p7	9:33332511	AGTGAAGGTATGACT[C/G]GGGTGGGGCATGAGG	4799
rs759988089	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33295931	CTTTATAAAACACAT[A/G]TTTTATTTATTTGTT	4799
rs760009492	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33316972	TTGAGCAGAAACTTA[A/G]CAAAGAAAAGCCTAC	4799
rs760099661	snp	C/G	1.64876e-05	0.00287116	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33311138	CCTGCCCACCCTGCC[C/G]TGCCTTTATGACAAA	4799
rs760110185	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33312153	ATCATGCAGATTTTC[G/T]GTGAGGTGCGTTTGT	4799
rs760142520	snp	G/T	4.9579e-05	0.00497866	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33295005	AACCGGAGGATGCTG[G/T]ACCCGAAAGTACCAA	4799
rs760153579	snp	C/T			synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33364067	TTTCAATATACGTTC[C/T]TCAGGGTCAAAATTC	4799
rs760170848	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33340066	GGAGGACAGTGGCCT[C/T]CTTCTCACAGCTCCA	4799
rs760195808	snp	A/G	1.65184e-05	0.00287384	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294932	GTATACAGCTATGGT[A/G]GAGGACCAAAAGTCA	4799
rs760268440	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33343906	CTTAGCTTTAATAAA[A/G]TAAAAGTTTAATAAA	4799
rs760270088	snp	C/G	1.69286e-05	0.0029093	intron-variant	NFX1	GRCh38.p7	9:33364117	ATGCCAGGTATGTAA[C/G]TTGTTACCTGCTTTC	4799
rs760272678	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33357161	CAAAAAATTAGCCGG[A/G]CATGGTGGCGGGCAC	4799
rs760286062	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33293475	TTCACTGCAACTCTT[G/T]GATATAGAGGTTGTT	4799
rs760316374	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33310557	TCCATGACCCCCTTC[A/C]CTTTCATTCTCTCCA	4799
rs760320130	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33320228	CCTTGGCCTCCCAAA[A/G]TGCTGGGATTATAGG	4799
rs760335735	snp	C/T	1.72178e-05	0.00293404	intron-variant, nc-transcript-variant	NFX1, LOC105376018	GRCh38.p7	9:33351518	AAACTCACCCCAAAT[C/T]CCACATGGAGATGAG	4799
rs760371386	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33324357	GTACTCCAGCCTGGA[C/T]GAGGGAGTAAGACTC	4799
rs760398081	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33304789	TTGAATATACTACCA[C/G]AAAGGCAGCATGAAA	4799
rs760406085	snp	A/G	1.64741e-05	0.00286998	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33301342	TGTCACGGCCCCAGT[A/G]TGGAGTTGTCAGAGC	4799
rs760416527	snp	C/T	1.64746e-05	0.00287002	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33367532	GGAAGTCCGTTTGTC[C/T]TCCTACCACGCTGAC	4799
rs760430195	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33309274	ATGCAGGAGAATGGC[A/G]TGAACCCGGGAGGCG	4799
rs760455623	snp	A/G	3.30764e-05	0.00406659	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352757	CAACTGATGGCCTAG[A/G]TGAAACAGATACATG	4799
rs760469956	snp	C/T	1.64846e-05	0.0028709	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33367613	ATCACAGACATCAGT[C/T]AGACAAGTAAGATTC	4799
rs760484173	snp	C/G			intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33364926	TTTCTCAAAACACAG[C/G]CATTATAACATCTGT	4799
rs760521498	in-del	-/C			intron-variant	NFX1	GRCh38.p7	9:33309800	GCCTGGTGTGAACAT[-/C]AATATTTTTAAAAGC	4799
rs760668568	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33336559	TAGTGAAGTGATATA[G/T]CACTACCACATGATG	4799
rs760699354	snp	A/C	0.000666611	0.0182445	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33342848	TGCCAGACATGCTGG[A/C]AAGCCAGTGAGTGTC	4799
rs760726943	snp	A/C	8.24056e-05	0.00641841	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294534	GGATTGGTAGAAGAA[A/C]TTACAGTTCACCACC	4799
rs760786103	snp	C/T	1.64738e-05	0.00286995	intron-variant	NFX1	GRCh38.p7	9:33344054	ATTCTTTTGTTTTAC[C/T]TGCTGCTCCACCAGG	4799
rs760801060	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33294140	TAATAAAATGAATAG[A/T]TGTATACATAGTACT	4799
rs760813679	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33344960	TGAGGTCAGGAGTTC[A/G]AGACCACTCTGGCCA	4799
rs760853945	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33293031	CTTTCAGGACAAATC[C/G]TGAATTGGGTGAGAG	4799
rs760911598	snp	C/T	1.6477e-05	0.00287024	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33366670	CTTCCCTCCCATGAA[C/T]AGAGACCACCGCCGG	4799
rs760932130	snp	A/C			missense, nc-transcript-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33351737	TGTGGTCACCCGTGT[A/C]TGGCACCCTGCCATA	4799
rs760979353	snp	A/T			intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33349472	TTGAGAACTACATTC[A/T]ACTAAAATATGGATT	4799
rs761009993	snp	A/G	1.65436e-05	0.00287602	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33366598	TTTTCAGAATGATAT[A/G]ATCAATCAGTCATCT	4799
rs761011350	snp	A/C	4.94303e-05	0.00497119	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33328594	AGATTTCATTCATAC[A/C]TGTGAAAAGCTCTGC	4799
rs761026248	snp	A/G			intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33353235	AAGGGAAGATGTCCT[A/G]AAGTTAGGTGAATTG	4799
rs761040535	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33301776	TATTTTTAATTTATC[A/T]TCTTCTCATTTTTGG	4799
rs761041774	snp	A/G	1.64808e-05	0.00287057	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33295194	CAAAACAGGAGGGCC[A/G]CCGACATACAAACGC	4799
rs761052925	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33342655	TTTATCCATAAATGT[A/G]TAGAGCTTTGTTTTT	4799
rs761079803	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33300581	TGAAATCTAGAAAGA[C/G]TTTGCTGCAATTGTG	4799
rs761099346	snp	G/T	0.000109399	0.00739511	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33332476	TTTTTCCATAGGAGC[G/T]TCCATGTACCAGTCT	4799
rs761131253	snp	G/T	3.29522e-05	0.00405894	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33295279	AGCAAAATCTACCTG[G/T]GACAGTGAGAACTTG	4799
rs761163839	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33308593	TCTTAGGTTCAAGTT[A/C]CTTAAATAGTTATGT	4799
rs761260477	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33315323	TGTCAGTTACCCAGT[C/T]GCTGATTAAACAGCC	4799
rs761277333	snp	C/T	1.65616e-05	0.00287759	intron-variant	NFX1	GRCh38.p7	9:33311098	TCAGTGAAACCTTTC[C/T]CTTTCAGTCTCTGCC	4799
rs761317568	snp	A/T	1.64955e-05	0.00287184	utr-variant-5-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33290537	GTGACAGTGCTGACT[A/T]GGCTGTACAGCTCGA	4799
rs761334335	snp	A/C	1.64977e-05	0.00287203	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33307297	CCCACATTCCTGTAA[A/C]CTGTAAGTTGGAATG	4799
rs761361763	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33323611	TACAAAAATTAGCTG[G/T]GCATGTTGGTATGCG	4799
rs761376733	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33356004	TGTTGGATATAAGCC[A/T]GAAGTAGAATTGCTG	4799
rs761378780	in-del	-/A			intron-variant	NFX1	GRCh38.p7	9:33317419	TGAGGCCCTGTCTCC[-/A]AAAAAAAAAAAAAAA	4799
rs761399788	snp	G/T	3.46542e-05	0.00416244	intron-variant	NFX1	GRCh38.p7	9:33363982	CCCTCCCACTCCTTT[G/T]ATTTGCATACCTCTC	4799
rs761432507	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33369343	GCTGAGATTACAGGC[A/G]TGAGCCACCACACCT	4799
rs761446543	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33300850	GACTTGGGCTTCTTA[C/T]AGCTGACACTACAGC	4799
rs761451648	in-del	-/G	1.65274e-05	0.00287462	intron-variant	NFX1	GRCh38.p7	9:33338473	ATGTTCATATCCTTT[-/G]TCTGGTTTTTTTTTT	4799
rs761470365	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33354907	AGTAAGTAGTTGCAG[C/T]TGCTTTTTTAATCTC	4799
rs761492650	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33363599	AAGAAATGTATAAAA[A/G]TGAAGTGTATATGTT	4799
rs761493015	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33367971	GGGCGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC	4799
rs761495400	snp	C/T	1.66801e-05	0.00288787	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33364093	AATTCAGTGATAGTT[C/T]GAAAGAAGATGCCAG	4799
rs761497155	snp	A/G	1.65627e-05	0.00287769	intron-variant	NFX1	GRCh38.p7	9:33346989	TGTATAATGGTTTAC[A/G]TGGCTTTATTTAGAA	4799
rs761508827	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33330459	GAAATTACAATATAC[A/G]TAGGATAACAGAGGC	4799
rs761527546	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33344565	ATTTATCGTATTAAA[A/C]TTAAGAAAATAGAGG	4799
rs761553051	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33317291	AGGTGTAGTGGCACG[C/T]ACCTGTACTCCCAGC	4799
rs761569890	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33322087	ATGCCTGCAATCCCA[A/G]CTACTCGGGAGGCTG	4799
rs761645639	snp	C/G	1.64768e-05	0.00287021	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33318999	CCCAGCTGGTGCGCT[C/G]TTGCCCCTGTGGCCA	4799
rs761709550	snp	C/T	3.29516e-05	0.00405891	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33367524	TATCAGGGGGAAGTC[C/T]GTTTGTCCTCCTACC	4799
rs761728109	snp	A/G	1.65209e-05	0.00287405	splice-donor-variant	NFX1	GRCh38.p7	9:33347118	ATGGGCAAGCATGAG[A/G]TAAGTTTTCTCTCTC	4799
rs761755725	snp	C/T	1.6486e-05	0.00287102	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352622	CAGTGTGCTAAAAGT[C/T]GTTCCATGTTCATCT	4799
rs761808158	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33296817	GCCCTCACGCTTATG[A/T]CTTTCTCTTAAATTT	4799
rs761811527	snp	C/T	1.65888e-05	0.00287996	intron-variant	NFX1	GRCh38.p7	9:33301463	TTATTCTCCCCTATT[C/T]GATACGTTTAAGTAT	4799
rs761826812	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33305558	CATGATTCTTTATGG[A/G]GATTAGTTTGGTAGC	4799
rs761829693	in-del	-/AGCACAGAG	1.65748e-05	0.00287874	cds-indel, nc-transcript-variant	NFX1	GRCh38.p7	9:33294754	TATCAGAGTCAAGAA[-/AGCACAGAG]TCTTGCTGAGCAGAC	4799
rs761833024	in-del	-/T			intron-variant	NFX1	GRCh38.p7	9:33353683	ATCTGATAGATTTGC[-/T]TTTTTTTTTTTTTTT	4799
rs761835654	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33310040	AAGAAACATGCTTAA[A/C]CTTATGTCTCCTATG	4799
rs761843438	snp	C/T	3.30104e-05	0.00406252	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33294506	GGGACTCAAAGGAGA[C/T]TAGACTCTAATAGGA	4799
rs761869989	snp	A/G			utr-variant-3-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33371107	AGCAGGAGACTTGAG[A/G]AGTAGAGTGACAAAA	4799
rs761874593	snp	A/G	1.64762e-05	0.00287016	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33301328	TGTGAATTGGTTCGT[A/G]TCACGGCCCCAGTGT	4799
rs761876492	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33343857	GTCATAGTAATAAAT[C/G]AAACTTCATATCTGT	4799
rs761896436	snp	A/G	0.000147427	0.0085844	intron-variant	NFX1	GRCh38.p7	9:33294374	CTATGAGTTTCATGG[A/G]TGAAGTTTAATCTCT	4799
rs761932714	in-del	-/AG			intron-variant	NFX1	GRCh38.p7	9:33363308	TTATTATTTTTAGAC[-/AG]AGTCTCACTGTGTTG	4799
rs761945226	in-del	-/T			intron-variant	NFX1	GRCh38.p7	9:33314953	AAAAAAAGTAGAAAG[-/T]TATCTACATGAATAG	4799
rs761965322	snp	A/G	3.94392e-05	0.0044405	intron-variant	NFX1	GRCh38.p7	9:33342718	AATGAAGACCATTTT[A/G]TGAACAAATATAAAT	4799
rs761966431	in-del	-/TTTG			intron-variant	NFX1	GRCh38.p7	9:33359866	AACTTGTCTTTGAAA[-/TTTG]TTTAAGATAAAAAGT	4799
rs761997550	snp	C/T			intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33350706	TTAAAAATACAGCTT[C/T]TAAGCTGGATGCAGT	4799
rs762020191	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33298861	GTTAGGAGGCTATTG[A/C]AGTTGTTCAGGTAGG	4799
rs762022938	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33304733	CAGAATCTCAGCCTT[A/C]ATAGATACTAAATTG	4799
rs762051619	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33318317	CTCCTCCACCACTAC[C/T]ACCAGCTTAGCTTGT	4799
rs762156342	snp	C/T	1.66735e-05	0.00288729	intron-variant, nc-transcript-variant	NFX1, LOC105376018	GRCh38.p7	9:33351548	GAATCTGGCTACTTC[C/T]GTCTCTCCTAGTTTC	4799
rs762174406	snp	C/G/T	0.00013201	0.00812335	synonymous-codon, missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33313784	CCTTGCCAGATCATT[C/G/T]TGAACCAGGGTAAGT	4799
rs762175151	snp	A/G	3.12994e-05	0.00395585	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33364852	AATCAAGTCCTGGAA[A/G]CACTTTCAACCTAGA	4799
rs762194419	snp	C/T	1.65004e-05	0.00287227	intron-variant	NFX1	GRCh38.p7	9:33313640	TGCTGTCTTTACATC[C/T]ATTGTCTTTACAGGC	4799
rs762213097	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33346600	TTCATTGTAGGAGGT[A/G]AGTTTTGATGAACCT	4799
rs762217638	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33316738	TAAGGCTGGCAACAG[C/G]GTCCTTTGGTTCCTT	4799
rs762278570	in-del	-/CT	0.000539882	0.016421	intron-variant	NFX1	GRCh38.p7	9:33363993	CTTTTATTTGCATAC[-/CT]CTCTCTCTCTTTCAG	4799
rs762288470	snp	A/G	1.64768e-05	0.00287021	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33313734	ACTGTGGTCAGCACC[A/G]GTGTGCTGAGCTGTG	4799
rs762307587	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33345156	AACAGAGTGAGACTC[C/G]ATCTCAAAAAAAGAA	4799
rs762334911	snp	C/T			intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33353461	AGATGGGGAGAGGTG[C/T]CATGGATATAGGACT	4799
rs762345135	snp	A/G	1.66983e-05	0.00288944	intron-variant	NFX1	GRCh38.p7	9:33328716	GTTGTTGCCATCAAT[A/G]TTTTCTTTAAAATGG	4799
rs762437306	in-del	-/A			intron-variant	NFX1	GRCh38.p7	9:33326414	CAAGCCTCTGTCTTT[-/A]AAAAAAAAAAAAAAA	4799
rs762447698	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33325621	GTGAGCCGAGATTGC[A/G]CCACTGCACTCCAGC	4799
rs762457413	snp	A/T	9.0841e-05	0.00673886	intron-variant	NFX1	GRCh38.p7	9:33354827	TGTATTCTGACTTTA[A/T]TTTTTTTTCATTTGC	4799
rs762503027	snp	A/G	6.63603e-05	0.00575984	intron-variant	NFX1	GRCh38.p7	9:33367653	TTTCCAAGGGGACCT[A/G]TCTGTCCAGAAAAGC	4799
rs762505412	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33367847	AGAGAGCAGTCACTG[G/T]ACATAATTTCCATGG	4799
rs762508897	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33321632	TATAATCTCAGCACT[G/T]TGGGAGGCCAAGGTG	4799
rs762577713	snp	A/G	8.23988e-05	0.00641815	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33307267	TTGTAGAAAGAAACA[A/G]CCTGGCCAGGACTGC	4799
rs762623475	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33333660	CCATGGTGGGTAAAG[C/G]TACACAACATCCACC	4799
rs762688098	snp	C/T	1.64727e-05	0.00286986	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33344094	ATTAACCTGCCATTG[C/T]GGTGCATCAGTGATT	4799
rs762704295	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33331038	AGGCACGGTGGTGGG[C/T]GCCTGTAGTCCCAGC	4799
rs762752283	in-del	-/A			intron-variant	NFX1	GRCh38.p7	9:33329878	GGCCAGGCTGGTCTC[-/A]AAACTCCTGACCTCA	4799
rs762791599	snp	C/G	3.29538e-05	0.00405904	intron-variant	NFX1	GRCh38.p7	9:33344219	TCTTCACACTTCAGC[C/G]TGCTCACACCATGTC	4799
rs762841245	snp	C/T	1.73649e-05	0.00294655	intron-variant	NFX1	GRCh38.p7	9:33363977	AGTTTCCCTCCCACT[C/T]CTTTTATTTGCATAC	4799
rs762855009	snp	A/C	1.65723e-05	0.00287852	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33294742	TGAGAAGCACCATAT[A/C]AGAGTCAAGAAAGCA	4799
rs762875485	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33357015	AAAAAAAAAATAAGC[C/T]GGGCATGGTGGCTCA	4799
rs762877353	in-del	-/GTTT			intron-variant	NFX1	GRCh38.p7	9:33291362	CAGTGAGGTTGGTTG[-/GTTT]GTTTTACAATCAGCA	4799
rs762900896	snp	A/G	1.65021e-05	0.00287241	utr-variant-5-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33290556	TGTACAGCTCGATCT[A/G]GGTTCTGCGGCACGG	4799
rs762945725	snp	A/C/T	1.65176e-05	0.00287376	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294663	CGTCTTTCCAGTCCT[A/C/T]TCCTTGTAATAAATC	4799
rs762974777	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33308333	TGTAGTCCCAGCTAC[C/T]TGGGAGGCTGAGCAA	4799
rs762981638	snp	A/G	1.64768e-05	0.00287021	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33301314	AGTGCATGGTGTGCT[A/G]TGAATTGGTTCGTGT	4799
rs762989502	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33307769	TCCAAGATGTCAAGA[C/T]GTCAATCTTTTTCTT	4799
rs763002693	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33354742	TGAGGGATTGTTTTT[C/T]GGCAAGAGTCAGCTG	4799
rs763025332	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33303674	TGGTATTTATAATCA[A/G]ATTTTTTATAAACCA	4799
rs763030054	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33306897	CGACTTGTCTTATAG[G/T]TATTTATCTTAAATT	4799
rs763036759	snp	C/T	1.72127e-05	0.00293361	intron-variant	NFX1	GRCh38.p7	9:33295443	GTAAACCTACCTAGA[C/T]AGGAAATATTTTGTT	4799
rs763036764	snp	A/C	1.64773e-05	0.00287026	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33318986	TGCCCACGGCTCCCC[A/C]AGCTGGTGCGCTGTT	4799
rs763066787	in-del	-/A	5.74256e-05	0.00535813	intron-variant	NFX1	GRCh38.p7	9:33354208	TTTTAAAATGCATAT[-/A]TGTGCCTTCTTTCTT	4799
rs763152361	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33363394	AGTTCAAGTGATTCT[C/T]ATGCCTCAGCCTCCT	4799
rs763180654	in-del	-/A			intron-variant	NFX1	GRCh38.p7	9:33292206	AGTATCTAATGAGGC[-/A]AAATCTTCTAGTCCA	4799
rs763191350	in-del	-/T	3.57923e-05	0.00423023	intron-variant	NFX1	GRCh38.p7	9:33369897	ATCATTCTTTGTTTG[-/T]TTTTTCAGGAATCCT	4799
rs763201703	snp	A/C	1.64977e-05	0.00287203	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33338533	TTTATGTGTGACAAG[A/C]GGTGTAACAAGAAAC	4799
rs763202907	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33330364	GCTAGTTTAATAGGA[A/C]AACTTCAGAAAAAAG	4799
rs763226840	in-del	-/TA			intron-variant	NFX1	GRCh38.p7	9:33341464	AACTGTATCAGTGTA[-/TA]TATATATATACATAA	4799
rs763259811	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33336696	GCCTTGATCTCCTGG[C/G]CTCCAGTGGTCCTCC	4799
rs763329918	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33361096	CTGGAAACATTTTCA[A/G]AGCTTTTTGCACAGA	4799
rs763346920	snp	A/T			upstream-variant-2KB	NFX1	GRCh38.p7	9:33289992	TACTGATGAGAATAA[A/T]CGCCTTTGTAAAAAA	4799
rs763379598	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33369520	CATGTTTGTCCCACT[A/G]TCAAAACTTCACAAG	4799
rs763385986	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33339135	AAAAATATAACGTAT[G/T]CTATATATGACATAA	4799
rs763436840	snp	C/T	4.29673e-05	0.00463485	intron-variant	NFX1	GRCh38.p7	9:33342698	GTTATTTATGGAAAA[C/T]ATAAAATGAAGACCA	4799
rs763507302	snp	C/T	1.64887e-05	0.00287125	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294620	CATAGTTATCATCCG[C/T]CAGGAAGCAAACCTA	4799
rs763526742	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33292120	TTTGAAGAAGAATTC[A/G]GTGGGGCCTAGTTGT	4799
rs763562413	snp	A/G	6.59315e-05	0.0057412	intron-variant	NFX1	GRCh38.p7	9:33303311	TCTTTTACTACATAC[A/G]TTGTACCTCAGTTCA	4799
rs763579424	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33290782	GTCTTCTTGGACTAG[A/G]TGGTGAAGCCCAGTA	4799
rs763583671	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33320679	GTCTGCAGTTTTGCA[A/G]TGACTTGGCAACTTC	4799
rs763656159	snp	C/G			upstream-variant-2KB	NFX1	GRCh38.p7	9:33289940	CTGTAAGGAGAGGAG[C/G]GGCGTTGGCAAATGT	4799
rs763680219	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33321681	AGGACTTTGAGACCA[G/T]CCTGGGCAACATGGC	4799
rs763723302	snp	C/T			intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33353566	GAGGGATTGAGTCAC[C/T]TCATCGCTTCCCATG	4799
rs763724178	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33326830	GGGTTTATAACATAT[A/G]GATGTGATATGTATA	4799
rs763733705	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33334533	AAGTTTAAAAAAAAA[A/T]ATGAAGTGAAAGATG	4799
rs763752139	snp	A/G	1.65732e-05	0.00287859	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294743	GAGAAGCACCATATC[A/G]GAGTCAAGAAAGCAC	4799
rs763761010	snp	A/G	5.18892e-05	0.00509332	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33369972	CTATTTTGACGTCCA[A/G]GACTAAGAAGATCAT	4799
rs763804988	snp	C/T	4.94401e-05	0.00497168	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33307270	TAGAAAGAAACAGCC[C/T]GGCCAGGACTGCCCA	4799
rs763832463	snp	C/T	2.02386e-05	0.00318102	intron-variant	NFX1	GRCh38.p7	9:33354836	ACTTTAATTTTTTTT[C/T]ATTTGCTTATCAAGG	4799
rs763842299	in-del	-/AG	3.2975e-05	0.00406035	utr-variant-5-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33290527	ACGTGACCTGGTGAC[-/AG]TGCTGACTTGGCTGT	4799
rs763871126	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33330378	AAAACTTCAGAAAAA[A/C]GGGAAAAGTAGTATA	4799
rs763882410	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33324066	GAGCACGTAGTGAGA[C/T]CCTATCTCTACAAAA	4799
rs763905305	snp	C/G	1.64773e-05	0.00287026	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33366685	CAGAGACCACCGCCG[C/G]ATCATCCATGACTTG	4799
rs763938891	snp	C/T			intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33351103	GAGCCCCGAGATTGG[C/T]GCCACTGTACTCCAG	4799
rs763971076	snp	A/G	1.76095e-05	0.00296723	intron-variant	NFX1	GRCh38.p7	9:33295451	ACCTAGATAGGAAAT[A/G]TTTTGTTGTCTTTTT	4799
rs764066701	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33359799	CTGCAAATTGTTAAT[A/C]ATTGGAGAATTTAGG	4799
rs764103006	snp	C/T	1.7327e-05	0.00294333	missense, nc-transcript-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33351761	TGCCATACCAGCTCA[C/T]CCTGCCCTGTGACTG	4799
rs764104282	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33340944	GGGCAAAGCCATTCA[A/G]CAAGTCTCTAGGAAG	4799
rs764113461	snp	G/T	3.32508e-05	0.00407729	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33366760	GAAGCGCAATGTGGT[G/T]GTCACTGCCATCAGG	4799
rs764114130	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33303686	TCAGATTTTTTATAA[A/G]CCAGCATTATAAACT	4799
rs764118180	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33336509	GTGAGCCACCGCACC[A/G]ACCATTTTTGGGGCT	4799
rs764147162	in-del	-/C			intron-variant	NFX1	GRCh38.p7	9:33331590	GGAACTTTTTCATAT[-/C]ATCAATCCCAGACAC	4799
rs764183625	snp	C/T	1.64822e-05	0.00287068	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33311150	GCCCTGCCTTTATGA[C/T]AAAAACATGTGAATG	4799
rs764241219	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33317198	CCAGGATGGGCTGAT[C/G]ACTTGAGCCCAGGAG	4799
rs764252060	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33337305	CATTTACATTATATT[C/T]GGTGTTATAAGTAAT	4799
rs764264385	in-del	-/TAAA			intron-variant	NFX1	GRCh38.p7	9:33301592	TTAAGTTATAGATCT[-/TAAA]TAAACCAGCTAAACA	4799
rs764273236	snp	G/T	4.95005e-05	0.00497471	utr-variant-5-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33290557	GTACAGCTCGATCTA[G/T]GTTCTGCGGCACGGG	4799
rs764308454	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33313574	GGTTTTGAGGGGAGA[G/T]TTAGGGGCCGCAGTG	4799
rs764322163	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33302172	TATTTTGATACAAGC[A/G]TACAATGTGTAATGA	4799
rs764343913	in-del	-/G	3.29289e-05	0.0040575	intron-variant	NFX1	GRCh38.p7	9:33342888	TAGTTTATTAGAAGA[-/G]TTTTTTAGAAATTCA	4799
rs764358489	snp	A/C			intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33349775	GAGTTGGGAGACATG[A/C]GGAGAGTTAAGTATT	4799
rs764374865	snp	G/T	4.24836e-05	0.00460869	intron-variant	NFX1	GRCh38.p7	9:33342706	TGGAAAATATAAAAT[G/T]AAGACCATTTTATGA	4799
rs764384109	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33325532	AGCCGGGCATGGTGG[C/T]GGGCACCTGTAGTCC	4799
rs764404273	in-del	-/TA			intron-variant	NFX1	GRCh38.p7	9:33361209	ACATAATTAGAAGAC[-/TA]TGAGCCATGAAGACA	4799
rs764416905	snp	A/G	1.65222e-05	0.00287417	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33294955	AAAAGTCAAGGGGAA[A/G]CTCAAATGTGAATGG	4799
rs764425708	snp	A/G	1.65012e-05	0.00287234	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33338534	TTATGTGTGACAAGC[A/G]GTGTAACAAGAAACG	4799
rs764428056	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33361110	AAAGCTTTTTGCACA[A/G]AGATATTAATTGTGT	4799
rs764434349	in-del	-/TT	1.64762e-05	0.00287016	intron-variant	NFX1	GRCh38.p7	9:33354816	GCTGTACAGTCTGTA[-/TT]CTGACTTTAATTTTT	4799
rs764462285	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33310695	TTACGGACCAGGTAG[A/G]TTTGAGTTCTATTAC	4799
rs764516387	snp	A/G/T	4.9576e-05	0.00497855	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33295016	GCTGGACCCGAAAGT[A/G/T]CCAAACCTGTGGGGG	4799
rs764541959	snp	C/T			utr-variant-3-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33370835	AACTGTCCTGTGTTG[C/T]TTTCCCTAGGCCTTC	4799
rs764552894	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33311181	TGGACGAACCAGGTA[A/G]AGTTAAAATTACACC	4799
rs764593231	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33369592	TGAACTGTGAAGGCA[C/G]AGTAAAATCATCATC	4799
rs764594075	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33324652	AAGAGATTTGGTCAG[A/G]CACAGTGGCTCATGC	4799
rs764609252	snp	A/G	1.73132e-05	0.00294216	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33364743	GTGACGTTGAGAAGG[A/G]AATGGAAACCCTCGT	4799
rs764618587	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33356436	TTCATTTTTTACTCT[C/G]TTGATGCCTTTTTTT	4799
rs764634764	snp	C/T	1.64776e-05	0.00287028	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33319040	AGCCAATTGCTAGAA[C/T]TTGGAAGTAGTAGTC	4799
rs764686786	snp	A/G	0.000477669	0.0154469	intron-variant, synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33347680	GTCCCACTACTGGGC[A/G]TCTACCCAGAAGAAA	4799
rs764716427	snp	A/G	1.6519e-05	0.00287388	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33319119	AGCCTCTGCCTTGTG[A/G]TTCCTTAGGTAACTA	4799
rs764732191	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33292263	CTTTAGTTTGATTTT[A/G]CTTTAGTTCCCATTC	4799
rs764899118	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33346347	TTCTTAAGTGTTTAT[G/T]GTATTTCTAACATGG	4799
rs764930143	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33298720	GCCCAGTGGGTCAAG[C/G]CTGCAGTAAGTAGTG	4799
rs764957343	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33300861	CTTATAGCTGACACT[A/G]CAGCTTCACGAGCCT	4799
rs764974514	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33293390	TGTGTTTCAGATCCT[C/G]TGTAGTCCTAACAGC	4799
rs764989805	snp	A/G	1.64827e-05	0.00287073	intron-variant	NFX1	GRCh38.p7	9:33303158	AGCTTTTGGAAGAAA[A/G]TTTATTTGGCCTACT	4799
rs765000713	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33341972	AATACAAAACTTACC[C/T]GGACATTGTTGTGGG	4799
rs765009422	snp	A/G	2.40001e-05	0.00346403	intron-variant	NFX1	GRCh38.p7	9:33354806	CTGGATGGGAGCTGT[A/G]CAGTCTGTATTCTGA	4799
rs765022164	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33327269	GGCTCAAGCAGTCCT[C/T]CCACCTTGGCTTCTC	4799
rs765025801	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33305960	GTGAGAAAAGGGTGT[A/G]ATGCAGAACACTTGC	4799
rs765060950	snp	C/G			missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294568	CTGTCACCTTTCCAG[C/G]CAGGTCCCTTATGAT	4799
rs765079224	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33327322	GAGCCACTGCACCCA[A/G]CCAAAAGCAGAAATT	4799
rs765084768	snp	A/T	5.3775e-05	0.00518504	intron-variant	NFX1	GRCh38.p7	9:33342874	GTGTCTTTACTGTAT[A/T]GTTTATTAGAAGAGT	4799
rs765123405	snp	A/G			intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33353378	GGGACCTGTGTAGCC[A/G]TACAGGGATCTGAGT	4799
rs765174526	snp	A/C	0.0148125	0.0847753	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33344083	GGTTTTGATGAATTA[A/C]CCTGCCATTGTGGTG	4799
rs765176387	snp	A/G	3.31521e-05	0.00407123	intron-variant	NFX1	GRCh38.p7	9:33313813	GTGGTGGGCACACCA[A/G]CTAGCAATGCTTGTG	4799
rs765230296	snp	A/G	1.67114e-05	0.00289057	intron-variant	NFX1	GRCh38.p7	9:33295431	AAACGCACACAGGTA[A/G]ACCTACCTAGATAGG	4799
rs765280402	snp	C/T	1.65119e-05	0.00287327	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33366617	AATCAGTCATCTTTT[C/T]CCTCAATACAGGGAA	4799
rs765307920	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33329037	GATAAAAGGACTCAC[C/T]GAACTTGCTGGTGGT	4799
rs765316135	snp	C/G	1.64982e-05	0.00287208	utr-variant-5-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33290551	TTGGCTGTACAGCTC[C/G]ATCTAGGTTCTGCGG	4799
rs765344674	snp	A/G	5.45628e-05	0.00522288	intron-variant	NFX1	GRCh38.p7	9:33332519	TATGACTGGGGTGGG[A/G]CATGAGGGAATTTCT	4799
rs765378259	in-del	-/AA	1.64849e-05	0.00287092	intron-variant	NFX1	GRCh38.p7	9:33338495	TTTTTTTTTCTTTTT[-/AA]TTTGCCACAGCAGAT	4799
rs765410019	snp	G/T	1.64779e-05	0.00287031	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33295322	AAGTCTTCCAGGAGG[G/T]TTGACCAAGAGAAAT	4799
rs765442784	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33314183	GAGATAGGGTTTCAC[A/C]ATGTTGGCCAGGCTG	4799
rs765453746	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33360889	AGCTTGTAAGTGACT[C/G]TTGGTGCAGTGTAAA	4799
rs765481026	snp	A/G	8.23825e-05	0.00641751	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33366681	TGAACAGAGACCACC[A/G]CCGGATCATCCATGA	4799
rs765551703	snp	C/G			upstream-variant-2KB	NFX1	GRCh38.p7	9:33289717	AAGCCAGGAAGGAAT[C/G]TGAATGGAGAATCAC	4799
rs765557226	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33324405	TAATAATTAAATTTA[G/T]CTGGGCATGGTGGCA	4799
rs765578531	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33369425	TAAAACTCTATTATG[A/G]AAATGTTTTAGAGTA	4799
rs765614714	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33316806	CTGTCACCTGCTCAT[A/G]TTTCTGTCTCTCGTG	4799
rs765617069	in-del	-/AATCTTTTTTGTTATTTTGTTTTTTAA	1.89356e-05	0.00307692	intron-variant	NFX1	GRCh38.p7	9:33301232	TTTTGTGTTTGAGTT[-/AATCTTTTTTGTTATTTTGTTTTTTAA]ACAGGTTCTCTAATT	4799
rs765638560	snp	C/T	8.50564e-05	0.00652081	intron-variant	NFX1	GRCh38.p7	9:33364125	TATGTAACTTGTTAC[C/T]TGCTTTCTTAATTGT	4799
rs765690645	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33358201	GTGATCTCGGCTCAC[C/T]GCAAGCTCCACCTCC	4799
rs765693218	snp	G/T	1.64868e-05	0.00287109	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33338520	AGCAGATGCTACATT[G/T]ATGTGTGACAAGCGG	4799
rs765733144	snp	C/T	1.65787e-05	0.00287907	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294764	AAGAAAGCACAGAGT[C/T]TTGCTGAGCAGACCT	4799
rs765744061	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33368245	CCATCTCAAAAAAAA[A/C]AGAATAGTTACTCTG	4799
rs765749371	in-del	-/AT			intron-variant	NFX1	GRCh38.p7	9:33357334	AATAAAGTATATCAA[-/AT]ATATATATATATATG	4799
rs765775985	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33313873	CTTGATAAACTTTGA[C/T]TGGTGTCAGACTTTT	4799
rs765801764	snp	C/G	1.64735e-05	0.00286993	intron-variant	NFX1	GRCh38.p7	9:33363999	TTTGCATACCTCTCT[C/G]TCTCTTTCAGGAGAT	4799
rs765803979	in-del	-/AG			intron-variant	NFX1	GRCh38.p7	9:33326050	AGTTGTGTTAGAATA[-/AG]AAAATGATACCAGAT	4799
rs765834749	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33345503	AGAGATAAAGTCAAA[A/C]GTTTGAAATTAAATA	4799
rs765854696	snp	A/G			intron-variant, utr-variant-3-prime	NFX1	GRCh38.p7	9:33348041	GAAAGGACGGGAGGC[A/G]GGTGAGGGATAAAAA	4799
rs765869641	snp	A/G	0.000136547	0.00826164	intron-variant	NFX1	GRCh38.p7	9:33347618	ACTGTGGAAAACTGT[A/G]GAGATTCCTTAAAGA	4799
rs765950663	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33356230	TTTTCCTGATGACTT[A/G]AGAGATTGAGCACCT	4799
rs765980673	snp	A/G	3.42331e-05	0.00413707	intron-variant	NFX1	GRCh38.p7	9:33366788	AGGTAGGTCAATCCC[A/G]CCGTCAGAGGAAGAA	4799
rs766005694	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33296293	CCTTACTCAACAGTC[C/G]CATCTTCTGCTGCCT	4799
rs766036038	snp	A/C	1.6473e-05	0.00286988	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33367539	CGTTTGTCCTCCTAC[A/C]ACGCTGACAGGTGTG	4799
rs766078175	snp	C/T	1.64817e-05	0.00287064	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294536	ATTGGTAGAAGAAAT[C/T]ACAGTTCACCACCTC	4799
rs766078939	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33310578	ATTCTCTCCATGTTA[C/T]TCACTAGCATGCCTC	4799
rs766129802	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33301152	ATATCCCTTAAAATC[C/T]CTGTGTTTGGATTCT	4799
rs766130876	in-del	-/A			intron-variant	NFX1	GRCh38.p7	9:33341181	AGTTTTAATGGACTT[-/A]ACAGTTCCAAGTGGC	4799
rs766138283	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33292443	TCCCTTTAGTCTGCC[C/T]TTCCCACCTGTTGGA	4799
rs766175062	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33305703	AGTAGTAGGAATGGG[A/T]GTCACCCAAAGTTTC	4799
rs766178202	snp	C/T			intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33351036	GTAACCCCAGCTACT[C/T]GGGAGGCTGAGGCTG	4799
rs766181742	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33331039	GGCACGGTGGTGGGC[A/G]CCTGTAGTCCCAGCT	4799
rs766183390	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33339411	ACTTATTCACTATCA[C/G]GAGAACAGCACAAGA	4799
rs766215554	in-del	-/AAAAC			intron-variant	NFX1	GRCh38.p7	9:33337741	TCTTTAAAACAAAAC[-/AAAAC]AAAACAAAACAAAAC	4799
rs766230183	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33320230	TTGGCCTCCCAAAGT[C/G]CTGGGATTATAGGTG	4799
rs766245605	snp	C/T	2.70508e-05	0.00367759	intron-variant	NFX1	GRCh38.p7	9:33342739	AAATATAAATCTCTT[C/T]TCCCAGGATAAGGAG	4799
rs766250425	snp	G/T	1.84184e-05	0.00303461	intron-variant	NFX1	GRCh38.p7	9:33294389	ATGAAGTTTAATCTC[G/T]TTACTGGCATGTCTA	4799
rs766263566	snp	A/G			intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33365135	AAAAATTAGCTGGGT[A/G]TGGTGGCGGGCACCT	4799
rs766307991	snp	A/G	0.000143718	0.00847575	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33342850	CCAGACATGCTGGCA[A/G]GCCAGTGAGTGTCTT	4799
rs766324581	snp	A/G	1.72806e-05	0.00293938	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33354123	TCTAAGATAACAGAC[A/G]TGCAGCTTGGAGGTT	4799
rs766329824	snp	C/T	1.66197e-05	0.00288263	intron-variant	NFX1	GRCh38.p7	9:33301470	CCCCTATTTGATACG[C/T]TTAAGTATTATTAAG	4799
rs766340986	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33328758	GGGGAGGAATCAAAA[C/T]AACCTCAGTAGATTA	4799
rs766365361	in-del	-/TTTTTTTTTTTTTTTTTTTTTT			intron-variant	NFX1	GRCh38.p7	9:33358648	CTGTGAATGGCTTGA[-/TTTTTTTTTTTTTTTTTTTTTT]TTTTTTTTTTTGATA	4799
rs766445841	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33340665	AACTTTTATGCTCTG[C/T]TTCCCTTTTAAAACT	4799
rs766496359	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33310516	GGCTAATTCTGACCT[A/G]TAGCATATCACTCAG	4799
rs766537287	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33314046	TGGAGTGCAGTGGCG[C/T]GATCCTAGCTCACTG	4799
rs766542107	in-del	-/ATAA			intron-variant	NFX1	GRCh38.p7	9:33331294	AAGTGAGTTTTCTAG[-/ATAA]ATAAAACATTTCTTA	4799
rs766586264	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33339304	ATGGTGGAAGGCAAG[A/G]AAGAGCAAGTCACTT	4799
rs766596948	in-del	-/G			intron-variant	NFX1	GRCh38.p7	9:33317435	AAAAAAAAAAAAAAA[-/G]GAAAGAAAGAAAAGA	4799
rs766650826	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33322259	ACCTCAAATGAAGAC[A/G]TATTTATTCAACAAA	4799
rs766710851	snp	C/G/T	3.29616e-05	0.00405954	missense, stop-gained, nc-transcript-variant	NFX1	GRCh38.p7	9:33295196	AAACAGGAGGGCCAC[C/G/T]GACATACAAACGCAG	4799
rs766780852	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33334883	TTTATAACTTTATGA[C/T]GCAAAATTTCAACCA	4799
rs766793150	snp	A/G	3.29516e-05	0.00405891	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33328596	ATTTCATTCATACCT[A/G]TGAAAAGCTCTGCCA	4799
rs766828155	snp	A/G	1.65031e-05	0.00287251	intron-variant	NFX1	GRCh38.p7	9:33307302	ATTCCTGTAACCTGT[A/G]AGTTGGAATGCTAAT	4799
rs766832068	snp	A/G			intron-variant, utr-variant-3-prime	NFX1	GRCh38.p7	9:33348256	ACTTGGGAGGCTGAG[A/G]CAGGAGAATTGCTTG	4799
rs766833043	snp	G/T	6.75504e-05	0.00581125	missense, nc-transcript-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33351738	GTGGTCACCCGTGTA[G/T]GGCACCCTGCCATAC	4799
rs766853213	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33301824	CGCCTGTAATCCCAG[C/T]GCTTTGGGAGGCCAA	4799
rs766859257	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33360421	AAAGCTCTTGGCACA[A/G]GAGCTTGGCACATAG	4799
rs766874196	snp	A/G	1.75431e-05	0.00296163	utr-variant-3-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33369982	GTCCAGGACTAAGAA[A/G]ATCATGATGCACTTA	4799
rs766885159	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33346949	TCTGAATTTAAAAGT[G/T]TCATGCCGTATGCCA	4799
rs766885210	snp	C/T	3.31369e-05	0.00407032	intron-variant	NFX1	GRCh38.p7	9:33307158	AGAATGTGGTTGAAG[C/T]TTGTACCATTGACTC	4799
rs766885247	snp	A/G	7.4638e-05	0.00610847	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33332480	TCCATAGGAGCTTCC[A/G]TGTACCAGTCTCAAA	4799
rs766918659	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33367332	CAAGCCACGGGCCTG[C/G]CATAGGTGGGTGGAA	4799
rs766956595	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33319559	CTGTCGCCCCAGCTC[A/G]AGTGCAGTGGTAGGA	4799
rs766975571	snp	C/T	1.70411e-05	0.00291895	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33354863	AAGGCTGGAGTGTGA[C/T]GAGGAGTGTTCAGCC	4799
rs766976116	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33318882	GCACTTTATGCAACA[A/G]TTATGTAATAGTGTG	4799
rs766982846	snp	A/G	1.65754e-05	0.00287879	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294749	CACCATATCAGAGTC[A/G]AGAAAGCACAGAGTC	4799
rs767023807	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33307095	ATAATAAAAACCACA[C/T]TAAAGTTGCATGCTG	4799
rs767037695	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33329266	AATATTGCCAACCAG[A/G]AAAGTTCACCCAGAC	4799
rs767045851	snp	C/T	1.65162e-05	0.00287365	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33294916	AAAAGCAACACAGTT[C/T]GTATACAGCTATGGT	4799
rs767053439	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33315379	GGCTGTTTAGTCATG[A/G]TACAACTCTAATCGT	4799
rs767065632	snp	A/G	1.72716e-05	0.00293862	intron-variant	NFX1	GRCh38.p7	9:33363989	ACTCCTTTTATTTGC[A/G]TACCTCTCTCTCTCT	4799
rs767092821	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33342562	CAGTATTGATCACCT[C/T]ATGACGAATTTTGTT	4799
rs767110744	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33296174	TCGGGTGATCCGCCT[C/T]GGCTTCCCAAAGTGC	4799
rs767188893	in-del	-/C			intron-variant	NFX1	GRCh38.p7	9:33331290	ACAGAAGTGAGTTTT[-/C]TAGATAAATAAAACA	4799
rs767202377	in-del	-/G			intron-variant	NFX1	GRCh38.p7	9:33338694	TTTAAAAGTCACTGG[-/G]ACAGGCCCCTAAGCA	4799
rs767206663	snp	C/T	1.6473e-05	0.00286988	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33344112	TGCATCAGTGATTTA[C/T]CCTCCAGTTCCCTGT	4799
rs767229216	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33354985	ACGTCATTCACTCAG[C/T]ACTGCGCTGCGTCTT	4799
rs767243668	snp	C/G	3.33572e-05	0.00408381	intron-variant	NFX1	GRCh38.p7	9:33347149	AAGTGCTCATTGTTC[C/G]AGGCAGAGGTTCATG	4799
rs767290817	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33368004	TTTGGGAGGCCAAGG[C/T]GGGTGGATCACTTAA	4799
rs767298535	snp	C/T	1.65359e-05	0.00287536	intron-variant	NFX1	GRCh38.p7	9:33347011	TATTTAGAAAGTATT[C/T]CTAAAGTTACCTTTC	4799
rs767320184	in-del	-/AT	1.65209e-05	0.00287405	frameshift-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33294948	AGGACCAAAAGTCAA[-/AT]GGGGAAACTCAAATG	4799
rs767323009	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33303971	ACTGAAACCGTATTC[A/G]GAAATTACCAATGGG	4799
rs767325028	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33317505	TATTTTAAAAATAAA[C/G]AGTCCTTGAATCTTA	4799
rs767328490	snp	A/G	1.65817e-05	0.00287933	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33338558	AGAAACGGTTGTGTG[A/G]ACGGCATAAATGTAA	4799
rs767328612	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33361648	CATGGTTGCGGGCGC[C/G]TGTAATCCCAGCTAC	4799
rs767363650	snp	A/C	1.6768e-05	0.00289546	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33366772	GGTGGTCACTGCCAT[A/C]AGGTAGGTCAATCCC	4799
rs767396216	snp	A/G	9.21226e-05	0.00678622	intron-variant	NFX1	GRCh38.p7	9:33294383	TCATGGATGAAGTTT[A/G]ATCTCTTTACTGGCA	4799
rs767403488	snp	A/G	1.8479e-05	0.0030396	intron-variant	NFX1	GRCh38.p7	9:33295459	AGGAAATATTTTGTT[A/G]TCTTTTTAATTTAAA	4799
rs767496239	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33292298	TTCGTATTTTAGCAT[C/T]ATCTTTAGCCCACAC	4799
rs767507491	in-del	-/G	4.95708e-05	0.00497825	intron-variant	NFX1	GRCh38.p7	9:33338476	TCATATCCTTTGTCT[-/G]GGTTTTTTTTTTCTT	4799
rs767563599	snp	A/C			utr-variant-3-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33371145	CTTAATTAAATTATA[A/C]AATTTAACTTTATAG	4799
rs767574057	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33355195	TAAGAGGTTTAAAAC[A/G]ATGTTTAGTTAACTT	4799
rs767614678	snp	G/T	1.71422e-05	0.0029276	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33364757	GAAATGGAAACCCTC[G/T]TGGAGGCCGTGAATA	4799
rs767627337	snp	A/G	1.64852e-05	0.00287094	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294524	GACTCTAATAGGATT[A/G]GTAGAAGAAATTACA	4799
rs767700064	snp	A/G	3.29772e-05	0.00406048	intron-variant	NFX1	GRCh38.p7	9:33342722	AAGACCATTTTATGA[A/G]CAAATATAAATCTCT	4799
rs767716580	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33339448	TGCCCCCACGATTCA[A/G]TTACCTCCCACCAGG	4799
rs767729899	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33313314	AAAGAGTGGGCCGGG[C/T]GTGGTGGCTCAAGCC	4799
rs767747313	in-del	-/CT	0.000539882	0.016421	intron-variant	NFX1	GRCh38.p7	9:33363992	CTTTTATTTGCATAC[-/CT]CTCTCTCTCTCTTTC	4799
rs767752736	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33339388	AGAAAGCCATCAGAT[C/T]TCATGAGACTTATTC	4799
rs767788724	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33304773	GAGGGAATAAATATT[C/T]TTGAATATACTACCA	4799
rs767807735	snp	C/G	1.6522e-05	0.00287414	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33295031	ACCAAACCTGTGGGG[C/G]TTTTCCACCCTGACT	4799
rs767808474	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33313903	TAGTCACAAAGACCT[G/T]GAGTAGAGAGAACTG	4799
rs767827749	in-del	-/T			intron-variant	NFX1	GRCh38.p7	9:33328194	TTCTTGTTTTTGTGC[-/T]TTTTTTTTTTTTGGT	4799
rs767851797	snp	A/T	1.65479e-05	0.0028764	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33366594	TTTGTTTTCAGAATG[A/T]TATGATCAATCAGTC	4799
rs767852818	snp	A/G			intron-variant, utr-variant-3-prime	NFX1	GRCh38.p7	9:33348052	AGGCGGGTGAGGGAT[A/G]AAAAACTACACACTG	4799
rs767865210	snp	A/G	4.94972e-05	0.00497455	intron-variant	NFX1	GRCh38.p7	9:33313641	GCTGTCTTTACATCT[A/G]TTGTCTTTACAGGCA	4799
rs767907828	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33346636	TATAGGCAGTAATGA[A/C]ATTGGAAGGAGTCAG	4799
rs767916554	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33310919	GGTGATAATGATGTC[A/G]ATTTTTTGCACATAA	4799
rs767955632	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33337016	CTGAGGCAAGAGAAT[C/T]GCTTGAACCCAGGAG	4799
rs767959999	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33298961	TGGAAGGAAGATTTT[A/G]TGCCTGAGCAACTTA	4799
rs767975109	snp	A/G	3.30022e-05	0.00406202	intron-variant	NFX1	GRCh38.p7	9:33328568	TTTCCAGCTCTTTTC[A/G]TTTTTATTAAAGATT	4799
rs768006910	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33312689	CAGGTGGGCCAACAT[A/G]GTGAAACCCCGTCTC	4799
rs768026485	snp	C/T	1.66749e-05	0.00288741	intron-variant	NFX1	GRCh38.p7	9:33319133	GGTTCCTTAGGTAAC[C/T]AGTAAGCGTAAAGTT	4799
rs768028419	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33357777	TCTCAAACTTCTGGC[G/T]CAAGCGAACCTCCTG	4799
rs768028637	snp	C/T	1.6571e-05	0.0028784	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33351703	CTGCAAGCAGCCCTG[C/T]ACCACCCCCAGAGCT	4799
rs768041373	snp	A/G	9.89218e-05	0.00703215	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33295161	AGGGGGCCAGGCCAC[A/G]ACCAGGCAGAAATCC	4799
rs768121378	snp	C/T			intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33365038	CAGCACTTTGGGAGG[C/T]CAAGGCAGGCAGATC	4799
rs768149583	snp	C/T	1.66346e-05	0.00288393	intron-variant	NFX1	GRCh38.p7	9:33367659	AGGGGACCTGTCTGT[C/T]CAGAAAAGCTAGCAG	4799
rs768198917	in-del	-/A			intron-variant	NFX1	GRCh38.p7	9:33337657	TCATTTGAGTGCAGG[-/A]ATTCGAGGTTACAGT	4799
rs768210300	snp	C/G	3.36717e-05	0.00410302	intron-variant	NFX1	GRCh38.p7	9:33332454	AAGTAGTTACCATTT[C/G]TTTTTCTTTTTCCAT	4799
rs768230654	snp	C/T			intron-variant, downstream-variant-500B	NFX1, LOC105376018	GRCh38.p7	9:33349198	GGCTAGGTTTGGGTG[C/T]TTTGGAAGTGAACGA	4799
rs768231655	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33356636	TATTTTACCTTTCAC[A/G]TTTTAAATCTACAGT	4799
rs768245203	in-del	-/TG	1.64746e-05	0.00287002	frameshift-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33328622	TGCCATGAAGGAGAC[-/TG]TGGACCATGCTCTCG	4799
rs768304472	in-del	-/CCAGAGCTG	1.66004e-05	0.00288096	cds-indel, nc-transcript-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33351711	AGCCCTGCACCACCC[-/CCAGAGCTG]ACTGTGGTCACCCGT	4799
rs768332281	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33344423	AAACGTTGGAAGACT[C/T]CCCAGCTGATCTTAT	4799
rs768373584	snp	A/G	1.65419e-05	0.00287588	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294869	AGTGAGAAGGAAGTT[A/G]TGGGTGCAGATCCCA	4799
rs768396681	snp	A/C	0.000104187	0.00721682	intron-variant	NFX1	GRCh38.p7	9:33363978	GTTTCCCTCCCACTC[A/C]TTTTATTTGCATACC	4799
rs768419684	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33301569	TCATGTGTTTCATAT[A/G]ACCAGAATTAAGTTA	4799
rs768434930	snp	C/T	0.00196078	0.0312497	intron-variant, utr-variant-3-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33347785	AACCAGCCCAACTGC[C/T]CATCAGTCAACAAGT	4799
rs768483022	snp	A/G	1.65258e-05	0.00287448	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294983	TGGAGTAACCGAACA[A/G]CTCCAAAACCGGAGG	4799
rs768518848	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33296764	CACATGTCCAGGGAA[C/G]CTTTTCTCACCTTTA	4799
rs768532351	snp	C/T	1.64844e-05	0.00287087	intron-variant	NFX1	GRCh38.p7	9:33311219	AGACCTCAGTTTTCA[C/T]ATGCATGATTGACTT	4799
rs768542746	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33343605	AGAAAGGACTTGACT[C/T]GGTGTTTTTATTCTC	4799
rs768549065	snp	A/G	1.64768e-05	0.00287021	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33367520	CTTTTATCAGGGGGA[A/G]GTCCGTTTGTCCTCC	4799
rs768579772	snp	C/T			upstream-variant-2KB	NFX1	GRCh38.p7	9:33289386	CCTCGGGTGTCCCTC[C/T]TCGAGCCCCTGCGGC	4799
rs768580361	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33309969	GAAAATTGTTTCACC[C/T]GAAAGGATTGAGGTA	4799
rs768587816	in-del	-/CCAAGGAG	1.69178e-05	0.00290837	frameshift-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33369938	ATTTACAGAAAATAA[-/CCAAGGAG]CCAATAATTGACTAT	4799
rs768595821	snp	C/T	3.29544e-05	0.00405908	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33318995	CTCCCCCAGCTGGTG[C/T]GCTGTTGCCCCTGTG	4799
rs768613904	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33309550	ACTTTCTTTTACTTT[C/G]AGGACCATAGAAGCC	4799
rs768646677	snp	A/G	1.65021e-05	0.00287241	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33347103	ACTCAGAAGTGGTGC[A/G]TGGGCAAGCATGAGG	4799
rs768668091	snp	C/T			utr-variant-3-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33370052	AGCAGATAAATCATG[C/T]CCGTTCCCCTCTGCC	4799
rs768699939	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33324201	CTGGCCAACATGGTG[A/C]AATCTCGTCTCTACT	4799
rs768701973	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33338902	GTCTTCGGCAGAAGA[G/T]TGTGTGTTGTCCCAA	4799
rs768703484	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33319795	GATTACAGGTGTAAG[C/T]CACTGTACCTGGCCA	4799
rs768719490	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33369305	CCTGACCTCGTGATC[C/T]GTCCGCCTTGGCCTC	4799
rs768744896	in-del	-/AGACTGGATAGAGTTCTA			intron-variant	NFX1	GRCh38.p7	9:33321485	CAGCTTCAGTATAAG[-/AGACTGGATAGAGTTCTA]CTTTAAAGATGGTAG	4799
rs768756671	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33332788	TATATGAAAAAATAT[A/G]TTAATGGTAGAATCT	4799
rs768771157	snp	A/G	4.94295e-05	0.00497115	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33301318	CATGGTGTGCTGTGA[A/G]TTGGTTCGTGTCACG	4799
rs768807628	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33331550	CATGAGTCACTTTTG[C/T]TTTATATCTGTAGAG	4799
rs768809838	snp	A/G	0.000115684	0.00760452	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33294499	AAATTGTGGGACTCA[A/G]AGGAGACTAGACTCT	4799
rs768832725	snp	C/G/T	2.09111e-05	0.00323344	intron-variant	NFX1	GRCh38.p7	9:33364700	TAACTGGTGATTTCT[C/G/T]ATTTCAGGAAGGACT	4799
rs768887823	snp	A/G	1.80091e-05	0.0030007	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33354093	TATTTCAGAATAGCT[A/G]CAATCTCCATGGCCT	4799
rs768912754	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33292870	AGCGAGAACTACACA[A/G]TACCCACTGGTCCAA	4799
rs768936628	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33347139	TTTCTCTCTCAAGTG[C/T]TCATTGTTCCAGGCA	4799
rs769015728	snp	A/G	1.65056e-05	0.00287272	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352735	GTTAGTGTTACTTAA[A/G]TGTTAACAACTGATG	4799
rs769022835	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33293975	CCTAAGTTCATACAA[C/T]AAGTTGGACAGGTGG	4799
rs769030891	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33326713	GACAAGAGTGGGACC[C/T]TGTCTCCAAAAATTA	4799
rs769038034	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33297870	TGATTAAGTCAGGCC[C/T]ACCCATACTCAAGGG	4799
rs769042634	snp	C/T	1.64784e-05	0.00287035	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33294580	CAGGCAGGTCCCTTA[C/T]GATGAAATCTCTGCT	4799
rs769140135	snp	A/G	1.64754e-05	0.00287009	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33313722	AGAATATTTTGAACT[A/G]TGGTCAGCACCAGTG	4799
rs769144020	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33335589	TCACTTTGTTGACCA[A/G]GCTGGTCTTGAATGC	4799
rs769179861	snp	A/G	2.76049e-05	0.00371506	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33364842	AAAAAAAAGCAATCA[A/G]GTCCTGGAAACACTT	4799
rs769188738	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33314873	TACCAAAAGATATCC[A/G]AAACCAATCAAAACT	4799
rs769195607	snp	C/T			synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33342808	TGGCCTTCATAGGTG[C/T]GAAGAACCTTGTCAT	4799
rs769234052	snp	C/G			intron-variant, utr-variant-3-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33347832	GTGTATCTATACGTA[C/G]CATGGAATACTACTC	4799
rs769234551	snp	A/G	0.000164823	0.00907659	intron-variant	NFX1	GRCh38.p7	9:33318692	TTTAAGAACCCATAC[A/G]TGTTACTAACGTTTT	4799
rs769264741	snp	C/G	1.64893e-05	0.0028713	utr-variant-5-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33290528	CGTGACCTGGTGACA[C/G]TGCTGACTTGGCTGT	4799
rs769285068	snp	A/G	4.99496e-05	0.00499723	intron-variant	NFX1	GRCh38.p7	9:33328710	GCTAGAGTTGTTGCC[A/G]TCAATGTTTTCTTTA	4799
rs769287620	snp	A/T	1.64757e-05	0.00287012	intron-variant	NFX1	GRCh38.p7	9:33344019	TTAGTATGTACTTGC[A/T]CATCCCAAACTCAGA	4799
rs769288291	in-del	-/C	1.64765e-05	0.00287019	frameshift-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33318939	GTAACCATACATGTT[-/C]GCAAGTGTGCCACCC	4799
rs769302256	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33299998	TTCTAGTTGTGTGAC[C/T]TTGGATAAATGATCT	4799
rs769338231	snp	C/T	1.67708e-05	0.00289571	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33351730	AGCTGACTGTGGTCA[C/T]CCGTGTATGGCACCC	4799
rs769340772	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33333146	TCACCACACCGGCCT[C/T]GATTCCTGTTTTTAT	4799
rs769384788	snp	A/C	1.6476e-05	0.00287014	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33295266	TCAATGAAAGACCAG[A/C]AAAATCTACCTGTGA	4799
rs769407132	snp	A/G	1.65111e-05	0.0028732	missense, nc-transcript-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33351680	GGGGAGTGTCTTGTG[A/G]ATGAGCCCTGCAAGC	4799
rs769495025	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33358754	TGCAGCCTCTACCTC[C/T]TGGGTTCAAGTGATC	4799
rs769528318	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33368969	GTCACTTTGGAAACA[C/T]GAGGGGTTTTCTCAG	4799
rs769562465	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33313583	GGGAGAGTTAGGGGC[C/T]GCAGTGTTAGTTTGG	4799
rs769575487	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33355492	TTATATTTTTGTGAC[A/G]TTCACTCCTGTTGTT	4799
rs769581738	snp	A/T	3.31757e-05	0.00407269	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33364048	TCAGTGAGGATTCTG[A/T]TCCTTTCAATATACG	4799
rs769612182	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33354598	CAGAGAGGCCATCAT[C/T]CCACCTGTCCTTCAG	4799
rs769619640	snp	C/G	3.31494e-05	0.00407107	intron-variant	NFX1	GRCh38.p7	9:33311084	TGGCTGTGGTTTATT[C/G]AGTGAAACCTTTCTC	4799
rs769656277	in-del	-/G			intron-variant	NFX1	GRCh38.p7	9:33321644	ACTTTGGGAGGCCAA[-/G]GTGGGAGAACTGCTT	4799
rs769699152	snp	A/G	1.65581e-05	0.00287728	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294717	ATCAACCTTGGCAGA[A/G]ATTGAGGAATGAGAA	4799
rs769703923	snp	C/T			upstream-variant-2KB	NFX1	GRCh38.p7	9:33290408	CACCTGGCGCGTCTA[C/T]CTGACGTCACGAACG	4799
rs769713950	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33335362	TAGCCTCCTGAGTAG[C/G]TGGAATTACAGGCAC	4799
rs769727357	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33331232	ATTTTTCATGAATAT[G/T]GATTTTTCATGACAT	4799
rs769735044	snp	A/G/T			intron-variant	NFX1	GRCh38.p7	9:33367795	TTGTTCCCACCAGAG[A/G/T]GGTCCTAAGTTTGTT	4799
rs769738932	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33323305	GGAGAGGGGAAGCAG[C/T]ATCCAGAGTTGCTAT	4799
rs769753244	snp	A/G	1.64792e-05	0.00287042	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33307217	AAGAATCCTGAGTGG[A/G]GCAGAAATGAAATTC	4799
rs769787881	snp	A/G	8.28494e-05	0.00643567	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33294823	CAGATCAGAGAGTGG[A/G]ACAGACCTCAGAGAG	4799
rs769795918	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33321526	ATGGTAGCATGAAGA[G/T]CTCCCATAGATCTGC	4799
rs769811928	snp	C/T			missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294968	AAACTCAAATGTGAA[C/T]GGAGTAACCGAACAA	4799
rs769820740	in-del	-/C			intron-variant	NFX1	GRCh38.p7	9:33315730	AGTCTCTAACAACAA[-/C]AAAAAAAAAAAATTA	4799
rs769937776	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33330345	TATAGTCCATAAATG[A/G]GAAGCTAGTTTAATA	4799
rs769941074	snp	C/T			intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33366614	ATCAATCAGTCATCT[C/T]TTCCCTCAATACAGG	4799
rs769979489	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33295630	TAGTTTTATGCATAT[C/T]ACAAGCAAATACAAA	4799
rs769986190	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33363186	ATAGTATATATGTAC[C/G]GAGACATCAACATCA	4799
rs770002799	snp	C/T	1.64806e-05	0.00287054	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33301303	AGAAAAATACGAGTG[C/T]ATGGTGTGCTGTGAA	4799
rs770021057	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33363373	CACTGCAACCTCTTT[C/G]TCCTGAGTTCAAGTG	4799
rs770111552	snp	A/G	0.000133094	0.00815654	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352455	GGGCATTGTGGACGG[A/G]GCAATTCTTTCCTAG	4799
rs770143877	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33305144	GAGGCGAATAAAACG[A/G]TTAACTTACCAGAGC	4799
rs770163267	snp	A/C/T			intron-variant	NFX1	GRCh38.p7	9:33347395	AAATATCCTTCATGC[A/C/T]CCTGTATACTCAATG	4799
rs770171072	snp	C/T	1.64966e-05	0.00287194	intron-variant	NFX1	GRCh38.p7	9:33367486	AACAATTCTCACTTT[C/T]CAATGCTTGGTGTTT	4799
rs770187015	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33338976	GTACTGCTTAGGTCA[G/T]GTCAGTAGGAAAAAT	4799
rs770203964	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33309580	CCATTCCCCAGTAGC[A/C]CTTTTCTGGTCTCCA	4799
rs770246849	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33363047	GGTGATGATGGTTAA[C/T]GGTAAGGTGTAGTAT	4799
rs770287119	snp	C/T	1.764e-05	0.00296979	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33342802	CCGTTGTGGCCTTCA[C/T]AGGTGTGAAGAACCT	4799
rs770325587	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33298212	ATTTTACATAGGTTG[A/T]CCTCTTTGATAAGGA	4799
rs770342678	snp	A/G	1.64844e-05	0.00287087	missense, nc-transcript-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352716	CATCTAGTACTTATC[A/G]AAGGTTAGTGTTACT	4799
rs770379467	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33364555	CTCTTTTGTTCTTCC[A/G]TCAGTCATCCTTCTG	4799
rs770384621	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33358536	AAATTACAAGGACTT[C/G]ATTTTAAAGCAAATG	4799
rs770416767	snp	G/T	1.64923e-05	0.00287156	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33295129	ATACCCACAGAAAAG[G/T]CCTCCCTGGGAAGTG	4799
rs770427707	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33339834	CAGTGGGGCAGTCAA[A/G]TCTTAAAGCTACAAA	4799
rs770430638	snp	C/T	6.56276e-05	0.00572796	intron-variant	NFX1	GRCh38.p7	9:33354078	TCCCTTTCTTTTTTA[C/T]ATTTCAGAATAGCTG	4799
rs770450230	snp	G/T	1.64955e-05	0.00287184	missense, nc-transcript-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33351657	AATGTCAGAGACTCT[G/T]TCACAAAGGGGAGTG	4799
rs770456972	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33359719	ACTCTATCAGATCAA[C/G]AGGCATTTATTCAAC	4799
rs770476536	snp	A/G	0.000103552	0.0071948	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33364838	GAAAAAAAAAAAGCA[A/G]TCAAGTCCTGGAAAC	4799
rs770540633	snp	A/G	1.77789e-05	0.00298146	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33364728	ACTTAAAGTTTGTCA[A/G]TGACGTTGAGAAGGA	4799
rs770599350	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33321287	AGAGGGTACCTGCTA[C/T]ACCTCAGCAGGTATC	4799
rs770618202	snp	C/G			utr-variant-3-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33370593	TCAATGTGATCAGTT[C/G]TAGACCTAGAAGGGG	4799
rs770628557	snp	C/T	1.72065e-05	0.00293308	intron-variant, nc-transcript-variant	NFX1, LOC105376018	GRCh38.p7	9:33351519	AACTCACCCCAAATC[C/T]CACATGGAGATGAGA	4799
rs770637796	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33336023	TTTTTGTTCCAATAC[C/T]TATTTTCATTTCTTT	4799
rs770645661	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33333793	TGCCTCAAAACCGTA[G/T]TTAAACTTTTGGTTC	4799
rs770699534	snp	A/G	1.64898e-05	0.00287135	splice-donor-variant	NFX1	GRCh38.p7	9:33367620	ACATCAGTCAGACAA[A/G]TAAGATTCTCCAGCT	4799
rs770749592	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33292716	ATATGAGTACATGCA[A/G]CCTTCTCTGGATTCT	4799
rs770823567	snp	A/G	4.21879e-05	0.00459262	intron-variant	NFX1	GRCh38.p7	9:33354231	TCTTTCTTCAATTAG[A/G]CTTCAATTAGAGGGC	4799
rs770840877	snp	A/G	1.64849e-05	0.00287092	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294609	CTGTTCATCAGCATA[A/G]TTATCATCCGTCAGG	4799
rs770845719	snp	A/G	1.65179e-05	0.00287379	intron-variant	NFX1	GRCh38.p7	9:33328683	TCAGAACAAAGGTAA[A/G]TCCTAAACAATGCTA	4799
rs770879767	snp	A/G	1.69436e-05	0.00291058	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33369952	ACCAAGGAGCCAATA[A/G]TTGACTATTTTGACG	4799
rs770900675	snp	G/T	1.6593e-05	0.00288031	intron-variant	NFX1	GRCh38.p7	9:33328534	TTGGGAGTATGAAAA[G/T]GAGTAGTTGCAGTTT	4799
rs770937663	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33332903	CAGGCCAGAGTGCAG[C/T]GGCGCGATCTCGGCT	4799
rs770937745	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33347593	GGTGGGAATGTAAAC[C/T]AGTACAACCACTGTG	4799
rs770937775	snp	A/G	1.64917e-05	0.00287151	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33307198	ATATGTTCTAGGCAA[A/G]GTAAAGAATCCTGAG	4799
rs770938824	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33369675	TGTAAATAGAGAATT[A/T]GTTATCTCACAGAAT	4799
rs770969884	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33299811	CTACACTCAGCAAGG[C/T]AGACAAAACTCTCCC	4799
rs770984807	in-del	-/T			intron-variant	NFX1	GRCh38.p7	9:33311557	CCAAAGTGACAAGGA[-/T]TTTTTTTTTTTTTGA	4799
rs771012756	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33328852	AGATCACTCTACCAA[A/C]TACAGGTGTGATAGT	4799
rs771050218	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33317791	GACCAGCCTGGCCAA[C/T]GTGGTGAAACTCCAT	4799
rs771066170	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33342178	AAAATATATTTTTTT[A/T]AAATTTCAAACTGGC	4799
rs771077223	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33354521	GGGGCACCTGTGGAG[C/G]ATTTGGGGCTGAGCA	4799
rs771116339	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33306666	GAGTCCATGGAAGAT[A/G]TGCCATGAAGATTTG	4799
rs771137618	snp	A/C	0.000214131	0.010345	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33318822	CAGCTGTTTAAAGAT[A/C]TGTGGCAAGTAAGGT	4799
rs771148447	snp	A/C	1.64757e-05	0.00287012	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33344187	TGAGTGTGACCATCC[A/C]GGTGAGTACCAACTT	4799
rs771152801	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33295458	TAGGAAATATTTTGT[C/T]GTCTTTTTAATTTAA	4799
rs771189815	snp	C/T	1.64879e-05	0.00287118	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33301287	TTGAACAACTAACAA[C/T]AGAAAAATACGAGTG	4799
rs771209135	snp	A/T	1.64765e-05	0.00287019	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33366673	CCCTCCCATGAACAG[A/T]GACCACCGCCGGATC	4799
rs771242528	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33292689	CCTCATGTCTAGTTG[A/G]ACATATCCTGTATAT	4799
rs771243168	snp	C/T	1.64754e-05	0.00287009	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33318974	CCCTGCCAGCAATGC[C/T]CACGGCTCCCCCAGC	4799
rs771251359	snp	A/G			intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33349509	CGATGGGAAATATGT[A/G]TGTCCTAGATGTTGG	4799
rs771286375	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33325698	AAGAAAACTGTCAAC[C/G]AAGAATCTTACATCT	4799
rs771292246	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33360776	TAACCAAAACATCAA[A/G]AGATCTTCCCCTAGA	4799
rs771353559	snp	A/G	2.35602e-05	0.00343213	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352451	AAGGGGGCATTGTGG[A/G]CGGGGCAATTCTTTC	4799
rs771370492	snp	A/G/T	4.96696e-05	0.00498324	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33295420	AAAGAATGTGGAAAC[A/G/T]CACACAGGTAAACCT	4799
rs771372990	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33303341	AGGAAAGGTGGTCTG[C/T]GGGGCATGTTTTAGA	4799
rs771385915	snp	A/T	0.000280368	0.0118366	intron-variant	NFX1	GRCh38.p7	9:33338495	TTTTTTTTTCTTTTT[A/T]ATTTGCCACAGCAGA	4799
rs771399317	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33318205	ATTTCTTTTTGGCAA[C/T]GGGGACCTTTTTACA	4799
rs771400720	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33329944	GATTACAGGTGTGCA[C/T]CACCACTCCTGGCTA	4799
rs771405424	snp	G/T	1.64974e-05	0.00287201	utr-variant-5-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33290541	CAGTGCTGACTTGGC[G/T]GTACAGCTCGATCTA	4799
rs771406711	snp	A/G			intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33350246	GAGGTGGAGGTTGCA[A/G]TGAGCTGAGATGGCG	4799
rs771427965	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33316914	TTGATTCTTTTGCTC[A/C]CAGCTTTCTATTCAT	4799
rs771452514	in-del	-/AAAAC			intron-variant	NFX1	GRCh38.p7	9:33334464	TATCTCTAAAACAAT[-/AAAAC]AAAATAATAAAAACA	4799
rs771461348	snp	A/G			synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33328600	CATTCATACCTGTGA[A/G]AAGCTCTGCCATGAA	4799
rs771496605	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33291793	CTGTAGTCCCAGCTA[C/T]TCCGGAGGCTGAGGC	4799
rs771549437	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33325206	TATAATAAAAATGCT[A/G]AAAGTTAATGATAAG	4799
rs771563414	snp	A/C/G	4.95858e-05	0.00497904	intron-variant	NFX1	GRCh38.p7	9:33313620	AACAGGAACTTTTAC[A/C/G]CTGATGCTGTCTTTA	4799
rs771602313	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33324294	TAAGGCAGGAGAATC[A/G]CTTGAACCCAGTAGG	4799
rs771651293	snp	C/G	3.30546e-05	0.00406524	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33295002	CAAAACCGGAGGATG[C/G]TGGACCCGAAAGTAC	4799
rs771723667	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33299547	AAAAAAATCAGCCAG[A/G]TATAGTGGCACACGC	4799
rs771764282	in-del	-/CGTGT	1.67944e-05	0.00289775	frameshift-variant, nc-transcript-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33351732	CTGACTGTGGTCACC[-/CGTGT]ATGGCACCCTGCCAT	4799
rs771795551	snp	G/T	4.95225e-05	0.00497582	utr-variant-5-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33290565	CGATCTAGGTTCTGC[G/T]GCACGGGATGGCGGA	4799
rs771848372	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33339993	GCTGTCATTGAGTGT[C/G]TGTGGCTTTTCCAGG	4799
rs771852347	snp	G/T	6.93289e-05	0.00588724	intron-variant	NFX1	GRCh38.p7	9:33319162	TTGGCTTTAAAAATA[G/T]TATTGTAAATGGTTG	4799
rs771913959	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33298091	GGAATTTACATTCTG[G/T]TAGGGAAGACAGGCA	4799
rs771924547	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33336469	TCCGCCTGCCTCAGC[C/T]TCTCAAAGTGCTGGG	4799
rs771952737	in-del	-/CTC	5.21952e-05	0.00510832	intron-variant	NFX1	GRCh38.p7	9:33366804	CCGTCAGAGGAAGAA[-/CTC]CTAAGCAGGGCAAAC	4799
rs771993876	snp	C/T	3.32602e-05	0.00407786	intron-variant	NFX1	GRCh38.p7	9:33301468	CTCCCCTATTTGATA[C/T]GTTTAAGTATTATTA	4799
rs772028768	in-del	-/TT			intron-variant	NFX1	GRCh38.p7	9:33307796	TCTTTCTTTCTTTCT[-/TT]TTTTTTTTTTTTTTT	4799
rs772042226	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33354295	AGAGCCTTGCATACA[A/C]AATAAGTATTCAATA	4799
rs772047064	snp	G/T	6.59087e-05	0.00574021	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33319095	CTTCATGTGGAAAAG[G/T]GTGCGGCAAGCCTCT	4799
rs772049576	snp	A/C	1.72925e-05	0.0029404	intron-variant, nc-transcript-variant	NFX1, LOC105376018	GRCh38.p7	9:33351512	AAGTTAAAACTCACC[A/C]CAAATCCCACATGGA	4799
rs772067131	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33344762	TCCCAGCTACTCGGG[A/T]GGCTGAGGCAGGAGA	4799
rs772075970	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33358406	TGGGATTACAGGCAT[G/T]AGCCACTGCGCCTGG	4799
rs772076541	snp	A/G	1.7151e-05	0.00292835	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33369915	TTTCAGGAATCCTGG[A/G]AGCAGTAATTTACAG	4799
rs772080987	snp	C/T	1.64741e-05	0.00286998	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33303240	GAATGTTTCTGCACA[C/T]GTTCCTAATACCTAC	4799
rs772105913	snp	C/T	1.76142e-05	0.00296762	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33354106	CTGCAATCTCCATGG[C/T]CTCTAAGATAACAGA	4799
rs772129698	snp	A/G	3.29636e-05	0.00405964	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294603	TCTCTGCTGTTCATC[A/G]GCATAGTTATCATCC	4799
rs772139645	snp	C/T	6.59141e-05	0.00574045	missense, nc-transcript-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33351621	TACCCTGCAGTGCCA[C/T]GCTACCATGTGGGAT	4799
rs772189300	snp	A/G			intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33364900	TCACAACTTCTTTGA[A/G]GATCCTTATCTTTCT	4799
rs772193536	snp	A/G	3.6806e-05	0.00428971	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33342825	AAGAACCTTGTCATC[A/G]TGGAAACTGCCAGAC	4799
rs772219716	snp	C/T	1.65285e-05	0.00287471	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294678	CTCCTTGTAATAAAT[C/T]GCCCAAGAGCCATGG	4799
rs772349633	snp	C/T	2.02067e-05	0.00317851	intron-variant	NFX1	GRCh38.p7	9:33354222	TATGTGCCTTCTTTC[C/T]TCAATTAGACTTCAA	4799
rs772400482	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33333917	TGGGAGGCCAAGGTG[G/T]GCGGATCACCTGAGG	4799
rs772421611	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33360701	AAATAAAAACCTAGC[A/T]GGCCAAATTCAGCCC	4799
rs772424888	in-del	-/C	1.9618e-05	0.00313187	intron-variant	NFX1	GRCh38.p7	9:33369862	GTCCTGTATCTGTTT[-/C]CCCCAAAGAAGAAAA	4799
rs772463761	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33315018	TTTTTGATGTTTTCA[C/G]TTTTTCTCTTCCTCT	4799
rs772509151	in-del	-/T			intron-variant	NFX1	GRCh38.p7	9:33323889	TAAAGAGATAGAAAC[-/T]TAGTTTTAAAAGAGG	4799
rs772521756	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33326289	GTGGTGGCATATGCC[C/T]GTGATCCCAGCTACT	4799
rs772553986	snp	C/T			missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33295239	ACATGGGCCCCATTC[C/T]AAAGGATGACCTCAA	4799
rs772554522	snp	A/G	1.68445e-05	0.00290206	intron-variant	NFX1	GRCh38.p7	9:33364111	AAGAAGATGCCAGGT[A/G]TGTAACTTGTTACCT	4799
rs772556996	snp	A/G	3.29451e-05	0.00405851	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33318790	GATGTAGGAAAGTCT[A/G]ATGGATTTGGGGATT	4799
rs772558982	snp	A/C/T	3.29518e-05	0.00405894	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33295277	CCAGCAAAATCTACC[A/C/T]GTGACAGTGAGAACT	4799
rs772584907	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33312040	CATTATAATACAAGG[C/T]CTCCTACATCATTAG	4799
rs772599798	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33328384	CAGTGTCTAAGCTGG[C/G]CCCTGAAGTTGTCAG	4799
rs772601342	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33302817	TGGGATTACAGGCGC[A/G]CACCACCACGCCCAG	4799
rs772614037	snp	G/T	1.64792e-05	0.00287042	intron-variant	NFX1	GRCh38.p7	9:33318708	TGTTACTAACGTTTT[G/T]TTTTTGAAATTTTCT	4799
rs772639464	snp	A/G	1.65187e-05	0.00287386	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294927	AGTTTGTATACAGCT[A/G]TGGTAGAGGACCAAA	4799
rs772646855	snp	C/T	3.29832e-05	0.00406085	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33295387	TCCTTTCTCCCGAGG[C/T]AAACAGAACCATGTG	4799
rs772649041	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33341541	GTATATAGCATACAT[A/C]ATTATTTTTTAAATT	4799
rs772651192	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33326982	GGACCATTAAGAAAA[C/T]AACTCAAAACATTTA	4799
rs772668043	snp	C/T	1.64901e-05	0.00287137	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33366724	TTATGGCCTGGAGAG[C/T]GTGAGCTATGACAGT	4799
rs772771313	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33356135	CTGTACATTTTTGTC[A/G]GCACTTGAAATTGTC	4799
rs772803308	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33324327	GAGGTTGCAGTGAGC[C/T]GAGATCGCACCACTG	4799
rs772820962	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33310490	AGCTCCTAAAATAGC[A/G]TTTTTCAGAGGGCTA	4799
rs772856084	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33291857	GCAGTGAGCCAAGAT[C/T]GTGCCACTGCACTCC	4799
rs772860393	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33337017	TGAGGCAAGAGAATC[A/G]CTTGAACCCAGGAGG	4799
rs772868104	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33300904	AATCCATGGATCTGA[C/T]AGATTTAGAGGATCC	4799
rs772878659	snp	G/T	4.95798e-05	0.0049787	stop-gained, nc-transcript-variant	NFX1	GRCh38.p7	9:33295004	AAACCGGAGGATGCT[G/T]GACCCGAAAGTACCA	4799
rs772904912	in-del	-/C			intron-variant	NFX1	GRCh38.p7	9:33315202	GCACTCCAGCCTGGG[-/C]CAACAAGAGCGGAAC	4799
rs772905633	snp	A/C			utr-variant-3-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33370450	GAATTTTTTAGTCTG[A/C]AATACCAAATAATGA	4799
rs772965225	snp	G/T	6.0381e-05	0.00549426	intron-variant	NFX1	GRCh38.p7	9:33364704	TGGTGATTTCTCATT[G/T]CAGGAAGGACTTAAA	4799
rs772984845	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33356201	ACAAGATGTCATTGA[A/G]CTTTTAATTTCTATT	4799
rs772990706	snp	A/G	3.295e-05	0.00405881	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33319010	CGCTGTTGCCCCTGT[A/G]GCCAAACTCCTCTCA	4799
rs772994810	snp	A/G	1.72196e-05	0.00293419	intron-variant, nc-transcript-variant	NFX1, LOC105376018	GRCh38.p7	9:33351515	TTAAAACTCACCCCA[A/G]ATCCCACATGGAGAT	4799
rs773005352	snp	C/G	1.64833e-05	0.00287078	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294528	CTAATAGGATTGGTA[C/G]AAGAAATTACAGTTC	4799
rs773025187	snp	C/T	1.64751e-05	0.00287007	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33367526	TCAGGGGGAAGTCCG[C/T]TTGTCCTCCTACCAC	4799
rs773047830	snp	C/G	1.66879e-05	0.00288855	intron-variant	NFX1	GRCh38.p7	9:33347151	GTGCTCATTGTTCCA[C/G]GCAGAGGTTCATGAT	4799
rs773078157	snp	A/G	1.64803e-05	0.00287052	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33367607	TTCCTCATCACAGAC[A/G]TCAGTCAGACAAGTA	4799
rs773080677	snp	C/T	1.64798e-05	0.00287047	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33319099	ATGTGGAAAAGTGTG[C/T]GGCAAGCCTCTGCCT	4799
rs773085463	in-del	-/A			intron-variant	NFX1	GRCh38.p7	9:33334467	CTCTAAAACAATAAA[-/A]CAAAATAATAAAAAC	4799
rs773104865	in-del	-/C			intron-variant	NFX1	GRCh38.p7	9:33346076	TAAAACAGAACTTAA[-/C]AAATTCTTCATTAAG	4799
rs773156073	in-del	-/G			intron-variant	NFX1	GRCh38.p7	9:33340417	AGGCTGCATGCAGCA[-/G]GGGGACCCTGGGGCC	4799
rs773175746	snp	A/G	1.64779e-05	0.00287031	intron-variant	NFX1	GRCh38.p7	9:33303273	TTGTTTCTGTGGTAA[A/G]TTTGTTTATATACAC	4799
rs773241268	in-del	-/T	1.68692e-05	0.00290419	frameshift-variant, nc-transcript-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33351738	GTGGTCACCCGTGTA[-/T]GGCACCCTGCCATAC	4799
rs773263205	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33346055	TGATTTTTTAAGTTA[A/G]TGGAGTAAAACAGAA	4799
rs773282504	snp	C/T	1.64727e-05	0.00286986	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33354107	TGCAATCTCCATGGC[C/T]TCTAAGATAACAGAC	4799
rs773288353	snp	A/T	1.64735e-05	0.00286993	intron-variant	NFX1	GRCh38.p7	9:33318728	TGAAATTTTCTCTTC[A/T]AGTATGCTATTGCGG	4799
rs773289316	snp	C/T	1.87503e-05	0.00306183	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33342832	TTGTCATCGTGGAAA[C/T]TGCCAGACATGCTGG	4799
rs773316074	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33344597	CAGGGCCAGGCGCAG[C/T]GGCTCATGCCTGTAA	4799
rs773328002	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33293008	CTAGAATTCTGCCTA[C/T]GTGAAAGCTTTCAGG	4799
rs773330529	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33315747	AAAAAAAAAAATTAG[C/T]CAGACATGGTGGCAT	4799
rs773345497	snp	C/T	1.64743e-05	0.00287	intron-variant	NFX1	GRCh38.p7	9:33344048	GAAAGGATTCTTTTG[C/T]TTTACCTGCTGCTCC	4799
rs773390069	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33339131	TATAAAAAATATAAC[A/G]TATGCTATATATGAC	4799
rs773433301	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33301585	ACCAGAATTAAGTTA[C/T]AGATCTTAAATAAAC	4799
rs773439653	snp	A/G	3.30868e-05	0.00406723	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33366596	TGTTTTCAGAATGAT[A/G]TGATCAATCAGTCAT	4799
rs773452960	snp	C/T			synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33366676	TCCCATGAACAGAGA[C/T]CACCGCCGGATCATC	4799
rs773468811	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33291929	TTGGAAAACACACTG[C/T]ATTGGTGTACCCTAG	4799
rs773505331	snp	A/G			intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33351845	TCTGAGGCTACTAGT[A/G]AATCCAGAACTGTCT	4799
rs773506099	snp	G/T			intron-variant, utr-variant-3-prime	NFX1	GRCh38.p7	9:33348129	GCCAAGGCAGGTAGA[G/T]TATGAGGTCGGGAGT	4799
rs773522181	snp	C/G/T	3.31462e-05	0.0040709	missense, nc-transcript-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33351705	GCAAGCAGCCCTGCA[C/G/T]CACCCCCAGAGCTGA	4799
rs773558836	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33322964	CTTACAGCAAAGACT[A/G]TTCCTTCCCAAATTT	4799
rs773576567	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33318127	GATTTTAAAAATGTG[A/T]TGTTTTTATAATACT	4799
rs773608362	snp	C/G	1.6492e-05	0.00287154	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33313770	GGGGTCAGTGCCAGC[C/G]TTGCCAGATCATTTT	4799
rs773669095	snp	C/T	1.64781e-05	0.00287033	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33366666	ACAGCTTCCCTCCCA[C/T]GAACAGAGACCACCG	4799
rs773700247	snp	A/T	3.60081e-05	0.00424297	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33332473	TTCTTTTTCCATAGG[A/T]GCTTCCATGTACCAG	4799
rs773753223	snp	G/T	6.73923e-05	0.00580445	missense, nc-transcript-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33351735	ACTGTGGTCACCCGT[G/T]TATGGCACCCTGCCA	4799
rs773755669	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33315032	AGTTTTTCTCTTCCT[C/T]TCCATTACTGCAATC	4799
rs773788139	snp	C/T	0.00175363	0.0295591	intron-variant	NFX1	GRCh38.p7	9:33338489	TCTGGTTTTTTTTTT[C/T]TTTTTAATTTGCCAC	4799
rs773789197	snp	G/T			intron-variant, utr-variant-3-prime	NFX1	GRCh38.p7	9:33348216	GCCGGGCCTGGTGGC[G/T]CATCCCTGTAATCCC	4799
rs773808937	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33313925	AGAGAACTGGAGATA[C/T]GATGCTTAGACGGTT	4799
rs773821463	in-del	-/G	1.66899e-05	0.00288871	frameshift-variant, nc-transcript-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33351723	CCCCCAGAGCTGACT[-/G]TGGTCACCCGTGTAT	4799
rs773863868	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33327036	TACACTATAAAAAAT[A/G]TTGACAAAATGCAAA	4799
rs773874168	snp	C/T	1.64996e-05	0.0028722	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33295399	AGGCAAACAGAACCA[C/T]GTGCTAAAGAATGTG	4799
rs773879588	snp	C/T			intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33350346	AAACGAAAAAATGGC[C/T]CTGCCATCAGTCTCA	4799
rs773905274	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33334638	ATGCCAGCATAGTTT[C/T]GTTTTTCCCTAGATT	4799
rs773934509	snp	C/G			utr-variant-5-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33290519	TCCGGGGCACGTGAC[C/G]TGGTGACAGTGCTGA	4799
rs773941577	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33369342	TGCTGAGATTACAGG[C/T]GTGAGCCACCACACC	4799
rs773945379	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33306805	TCCCCCCTTTCCCCA[C/T]GGTGCTCTTCTCTTA	4799
rs773964858	snp	C/T	1.65018e-05	0.00287239	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33347104	CTCAGAAGTGGTGCA[C/T]GGGCAAGCATGAGGT	4799
rs773972105	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33335624	TCTCAAGTGATCCTC[C/T]CATGTTGGCCTCCCA	4799
rs773981565	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33323569	ACCAGCCTGGCCGAC[A/G]TGGTGAAACCCCATC	4799
rs774024515	snp	A/G			intron-variant, downstream-variant-500B	NFX1, LOC105376018	GRCh38.p7	9:33349212	GCTTTGGAAGTGAAC[A/G]AGACTAACCCTTGCC	4799
rs774029795	snp	A/G	1.65141e-05	0.00287346	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294908	AAACCCAAAAAAGCA[A/G]CACAGTTTGTATACA	4799
rs774052053	snp	G/T	1.64863e-05	0.00287104	intron-variant	NFX1	GRCh38.p7	9:33344240	ACACCATGTCATTTA[G/T]GATCCTGCTGTGTTA	4799
rs774102134	in-del	-/T			intron-variant	NFX1	GRCh38.p7	9:33336226	TTTTTTTGGTTTTTG[-/T]TTTTTTTGAGATGGA	4799
rs774118140	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33309989	GGATTGAGGTATATA[A/T]AAAATATAACTGTTG	4799
rs774173112	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33324215	GAAATCTCGTCTCTA[C/T]TAAAAATATAAAAAT	4799
rs774187610	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33355972	AAACTTGCTTGCTCT[A/G]TATTTCTGTACATTT	4799
rs774229685	in-del	-/TG	4.75636e-05	0.00487642	intron-variant	NFX1	GRCh38.p7	9:33332510	AAGTGAAGGTATGAC[-/TG]GGGTGGGGCATGAGG	4799
rs774237141	in-del	-/TTT			intron-variant	NFX1	GRCh38.p7	9:33307795	TTCTTTCTTTCTTTC[-/TTT]TTTTTTTTTTTTTTT	4799
rs774257704	snp	A/G	6.59044e-05	0.00574002	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33301326	GCTGTGAATTGGTTC[A/G]TGTCACGGCCCCAGT	4799
rs774259888	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33344434	GACTCCCCAGCTGAT[C/G]TTATCTCTCAAGAAC	4799
rs774279256	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33292278	GCTTTAGTTCCCATT[C/T]CATGTTCGTATTTTA	4799
rs774281204	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33298060	AAGCACTGTTCTAGG[A/T]ACAGGGAATGCTGAT	4799
rs774292124	in-del	-/T			intron-variant	NFX1	GRCh38.p7	9:33296719	CAGAGCAAGACCCTG[-/T]TTTTGCGGGGGGAAA	4799
rs774318791	in-del	-/CAGACGT	1.65056e-05	0.00287272	frameshift-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33294644	AAACCTAAGAGTCAG[-/CAGACGT]CTTTCCAGTCCTCTC	4799
rs774323527	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33356818	ACTTGGCAAAACCTC[A/T]TCTGTACAAAAAATA	4799
rs774331623	snp	C/T	1.64762e-05	0.00287016	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33319083	TGGACCCTGTGCCTT[C/T]ATGTGGAAAAGTGTG	4799
rs774338907	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33304660	TTCCTTTGTTATTCT[C/T]TGTCTCACTTTGGCC	4799
rs774338992	snp	A/G	1.64751e-05	0.00287007	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33367590	ACGGCCTCCACCACC[A/G]ATTCCTCATCACAGA	4799
rs774349439	snp	A/G	1.84344e-05	0.00303593	intron-variant	NFX1	GRCh38.p7	9:33294372	GTCTATGAGTTTCAT[A/G]GATGAAGTTTAATCT	4799
rs774364234	in-del	-/TTTTT			intron-variant	NFX1	GRCh38.p7	9:33354071	CTCTTTTTCCCTTTC[-/TTTTT]TATATTTCAGAATAG	4799
rs774387246	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33296087	GCCCGCCACCATGCT[C/T]GGCTGATTTTTGTAT	4799
rs774444222	snp	C/T	1.65091e-05	0.00287303	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352736	TTAGTGTTACTTAAA[C/T]GTTAACAACTGATGG	4799
rs774446752	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33308585	GGTTTAAATCTTAGG[A/T]TCAAGTTACTTAAAT	4799
rs774457761	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33319829	AACTAAAATTGTAAG[A/T]ACAATAGAACCTCAG	4799
rs774480595	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33305519	TTCATTTGGAAGGCT[A/G]TGGGAAGCCACTGAG	4799
rs774553843	in-del	-/AAAG			intron-variant	NFX1	GRCh38.p7	9:33323822	AGGGAAACCATACTT[-/AAAG]AGGTAAAGAAAGATG	4799
rs774567112	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33312982	CCTGAAGCAAAGTCA[C/T]ATATAGTATGTTCTA	4799
rs774580086	snp	A/G	1.65187e-05	0.00287386	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294501	ATTGTGGGACTCAAA[A/G]GAGACTAGACTCTAA	4799
rs774585416	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33342219	AACCCCCCAGCACTT[C/T]GGGAGGCCAAGGTGG	4799
rs774642385	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33326840	CATATAGATGTGATA[A/T]GTATAACAATAACTG	4799
rs774643400	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33358770	TGGGTTCAAGTGATC[C/T]TCCCACCTCACCTCC	4799
rs774673524	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33339407	TGAGACTTATTCACT[A/G]TCACGAGAACAGCAC	4799
rs774678744	in-del	-/CTATTT	1.70012e-05	0.00291553	cds-indel, nc-transcript-variant	NFX1	GRCh38.p7	9:33369957	GGAGCCAATAATTGA[-/CTATTT]TGACGTCCAGGACTA	4799
rs774696495	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33295519	TTAGAAAGCAGAAAG[C/T]ATGGAAAGTTACACT	4799
rs774708136	snp	C/T	1.83397e-05	0.00302812	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33342823	TGAAGAACCTTGTCA[C/T]CGTGGAAACTGCCAG	4799
rs774708199	snp	A/T			intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33350636	TCTTCATCTCAAACT[A/T]ACCTTTCAGACTTTG	4799
rs774757298	snp	A/G	4.06529e-05	0.0045083	intron-variant	NFX1	GRCh38.p7	9:33342713	TATAAAATGAAGACC[A/G]TTTTATGAACAAATA	4799
rs774797953	snp	A/G	1.6476e-05	0.00287014	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33313728	TTTTGAACTGTGGTC[A/G]GCACCAGTGTGCTGA	4799
rs775025749	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33301496	TTAAGCCCAGCTTTA[A/C]AAATACAGTTTAATT	4799
rs775027341	snp	A/G	3.29587e-05	0.00405934	intron-variant	NFX1	GRCh38.p7	9:33318701	CCATACATGTTACTA[A/G]CGTTTTGTTTTTGAA	4799
rs775029226	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33339259	ATTAATGGATCTACA[G/T]TTCCAAGTCGGTGGG	4799
rs775088732	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33300310	CCTCATGATCTGCCC[A/G]CCTTGGCCTCCCAAA	4799
rs775102060	snp	C/T	1.7406e-05	0.00295003	intron-variant	NFX1	GRCh38.p7	9:33363973	AGATAGTTTCCCTCC[C/T]ACTCCTTTTATTTGC	4799
rs775158626	in-del	-/AATATT	0.000689643	0.0185566	intron-variant	NFX1	GRCh38.p7	9:33319140	AGGTAACTAGTAAGC[-/AATATT]GTAAAGTTGGCTTTA	4799
rs775175046	snp	C/T			intron-variant, utr-variant-3-prime	NFX1	GRCh38.p7	9:33347982	GCTAAGCTATGAGGA[C/T]GCAAAGGCATGAGAA	4799
rs775187592	snp	C/G	3.29549e-05	0.00405911	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33307249	ACATAGCTGTGGTGA[C/G]GTTTGTAGAAAGAAA	4799
rs775200609	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33354509	GGGCTGTTAAGAGGG[A/G]CACCTGTGGAGCATT	4799
rs775205417	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33342096	ACTCCAGCCTGGGCA[A/G]CAGAGTGAGACCCTG	4799
rs775217185	snp	A/C			intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33350994	ACTAAAAATACAAAA[A/C]TTAGCTGGTCGTGGT	4799
rs775263541	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33309273	GATGCAGGAGAATGG[C/T]GTGAACCCGGGAGGC	4799
rs775292133	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33355715	AATGGCATGATCTTG[A/G]CTCACTGCCACCTCT	4799
rs775292986	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33335374	TAGCTGGAATTACAG[C/G]CACCCACCACCATGC	4799
rs775333664	snp	G/T	3.29527e-05	0.00405898	intron-variant	NFX1	GRCh38.p7	9:33344214	ACTTGTCTTCACACT[G/T]CAGCCTGCTCACACC	4799
rs775345655	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33295767	AACAAGTGGTGGGTG[A/G]TAACATCTCTGCTGC	4799
rs775393859	snp	C/T	1.64738e-05	0.00286995	intron-variant	NFX1	GRCh38.p7	9:33318880	CTGCACTTTATGCAA[C/T]AATTATGTAATAGTG	4799
rs775482135	snp	C/G	6.70466e-05	0.00578954	intron-variant	NFX1	GRCh38.p7	9:33295433	ACGCACACAGGTAAA[C/G]CTACCTAGATAGGAA	4799
rs775483701	snp	C/T	1.64773e-05	0.00287026	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33318983	CAATGCCCACGGCTC[C/T]CCCAGCTGGTGCGCT	4799
rs775488309	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33340065	TGGAGGACAGTGGCC[G/T]TCTTCTCACAGCTCC	4799
rs775488644	snp	A/T	1.64844e-05	0.00287087	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33347090	TTGCACTTTCCTAAC[A/T]CAGAAGTGGTGCATG	4799
rs775515979	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33323414	CCTTGTGAGAGTGAC[C/T]AGATGTCAGATTTCA	4799
rs775544064	snp	A/G	1.66754e-05	0.00288746	intron-variant	NFX1	GRCh38.p7	9:33290625	CCCGAGCGGGACTGG[A/G]CCCCTTTCAGGGAGC	4799
rs775572690	snp	A/G	1.64953e-05	0.00287182	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33338531	CATTTATGTGTGACA[A/G]GCGGTGTAACAAGAA	4799
rs775589926	snp	A/G	4.97071e-05	0.00498509	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294827	TCAGAGAGTGGGACA[A/G]ACCTCAGAGAGCATA	4799
rs775612952	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33331374	TAAATGTATGCTGTG[G/T]CTATGTCTTCATAAA	4799
rs775653865	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33316086	TCTGTGGAATAGAAC[G/T]TCAAGGCTTCCATCA	4799
rs775657209	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33363198	TACCGAGACATCAAC[A/G]TCAAACTGCTTCATA	4799
rs775667668	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33330346	ATAGTCCATAAATGG[A/G]AAGCTAGTTTAATAG	4799
rs775697318	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33342305	TCTCTACTAAAAATA[A/C]AAAAAAATTAGCCAG	4799
rs775712673	snp	G/T	1.64779e-05	0.00287031	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33301309	ATACGAGTGCATGGT[G/T]TGCTGTGAATTGGTT	4799
rs775726099	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33300265	AGATGGGGTTTCACC[A/G]TGTTGGCCAGGATGG	4799
rs775742113	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33344897	CCAGGCACAGTGGCT[C/T]ATGCCTGTAATCCTA	4799
rs775751251	snp	A/G	8.28192e-05	0.00643449	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33366750	ACAGTGAACCGAAGC[A/G]CAATGTGGTGGTCAC	4799
rs775773172	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33339129	TATATAAAAAATATA[A/G]CGTATGCTATATATG	4799
rs775837177	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33360960	AAAAATAAAATAACT[C/T]GAATGTTGGTGAGAT	4799
rs775838582	snp	C/T	4.94205e-05	0.0049707	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33313700	GTCCACTGTTCTAAC[C/T]CATGTGAGAATATTT	4799
rs775851524	snp	A/G	3.29696e-05	0.00406001	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352717	ATCTAGTACTTATCA[A/G]AGGTTAGTGTTACTT	4799
rs775866659	snp	A/G	7.01434e-05	0.00592172	intron-variant	NFX1	GRCh38.p7	9:33338638	TTCATCCAGGTGCTG[A/G]GCTTCTGGAAGCCTG	4799
rs775877278	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33303626	CAGTATGAGTAAATA[A/G]TAGTGTTTATTTTAA	4799
rs775956279	snp	A/G	3.30551e-05	0.00406528	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33295010	GAGGATGCTGGACCC[A/G]AAAGTACCAAACCTG	4799
rs775956984	snp	A/G	1.71287e-05	0.00292644	intron-variant, nc-transcript-variant	NFX1, LOC105376018	GRCh38.p7	9:33351523	CACCCCAAATCCCAC[A/G]TGGAGATGAGAATCT	4799
rs775971071	snp	A/T			intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33366535	CTAAAATCACCTCTT[A/T]TTGATCCCTGCAATT	4799
rs775981113	snp	A/T	1.68414e-05	0.0029018	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294475	TCAGGAGAAAAAAAA[A/T]TCTGGTCTAAATTGT	4799
rs775996622	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33292760	CTCATTACTGCTTAA[C/T]GAGAAACACTCTTTT	4799
rs776020166	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33296161	CAAACTTCTGACCTC[G/T]GGTGATCCGCCTCGG	4799
rs776049473	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33291986	TGGGGTTGGAAAACT[C/T]TTTGGGCTGGGTATT	4799
rs776073485	snp	A/C	1.64917e-05	0.00287151	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33295131	ACCCACAGAAAAGGC[A/C]TCCCTGGGAAGTGGA	4799
rs776074926	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33318532	TCCTATGGTAAAGCT[C/T]TTAGGCGGGTCTTAG	4799
rs776099743	snp	C/G	1.65211e-05	0.00287407	intron-variant	NFX1	GRCh38.p7	9:33313627	ACTTTTACACTGATG[C/G]TGTCTTTACATCTAT	4799
rs776105034	snp	A/T			intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33351329	GCTGGGCGTGGTGGC[A/T]TGCACCTGCAATCCC	4799
rs776107583	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33299860	CTCAGGGTGTTCTCT[A/C]TTTCTTTTGACATTA	4799
rs776112396	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33356692	TGGATAAGGAGAGTT[C/T]ACAATTCAGCTTTTT	4799
rs776151437	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33325392	CAACTGGCCGGGCGC[A/G]GTGGCTCACGCCTGT	4799
rs776156665	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33313370	GAGGCAGGAGGATCG[A/C]TTAAGCCTAGGAGTT	4799
rs776274787	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33300478	GCAAATAACAATAAT[A/G]TTATGAAATAAATGC	4799
rs776331682	snp	A/G	1.70237e-05	0.00291746	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33369959	AGCCAATAATTGACT[A/G]TTTTGACGTCCAGGA	4799
rs776370370	snp	A/G	1.71402e-05	0.00292742	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33354143	GCTTGGAGGTTCAGT[A/G]GAGATCAGCAAGTTA	4799
rs776385598	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33320260	GTGAGCCACCATGCC[C/T]GGCTGGATGAATATT	4799
rs776386236	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33327008	ATTTAGTGAAAAATA[C/T]AATTAAGGGAATTAC	4799
rs776387616	snp	A/G	1.64996e-05	0.0028722	missense, nc-transcript-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33351668	CTCTGTCACAAAGGG[A/G]AGTGTCTTGTGGATG	4799
rs776453170	snp	A/G	1.6486e-05	0.00287102	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294612	TTCATCAGCATAGTT[A/G]TCATCCGTCAGGAAG	4799
rs776461378	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33347630	TGTGGAGATTCCTTA[A/C]AGAACTAAAAGTAGA	4799
rs776485537	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33312754	CACGTGCCTGTAGCC[C/T]CAGCTACTGGGGAGG	4799
rs776504483	snp	A/G	3.29592e-05	0.00405938	intron-variant	NFX1	GRCh38.p7	9:33303291	TGTTTATATACACTG[A/G]AGTCTCTTTTACTAC	4799
rs776533877	snp	A/G			missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33366752	AGTGAACCGAAGCGC[A/G]ATGTGGTGGTCACTG	4799
rs776544249	snp	C/T	1.64732e-05	0.0028699	intron-variant	NFX1	GRCh38.p7	9:33344066	TACCTGCTGCTCCAC[C/T]AGGTTTTGATGAATT	4799
rs776599276	snp	C/T	2.12632e-05	0.00326055	intron-variant	NFX1	GRCh38.p7	9:33354232	CTTTCTTCAATTAGA[C/T]TTCAATTAGAGGGCA	4799
rs776602469	snp	A/G	1.65433e-05	0.002876	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294693	CGCCCAAGAGCCATG[A/G]CCTTCAGAATCAACC	4799
rs776605074	snp	A/G			upstream-variant-2KB	NFX1	GRCh38.p7	9:33289138	GCCTCCTGGCCTGCC[A/G]CCCCACCCCAGCGTT	4799
rs776624575	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33295542	GTTACACTGTAAAAA[A/G]TCTCAATCTTTATTC	4799
rs776633540	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33321374	GTGGCTAGCGATAAC[A/G]ATGACTGTCAGGTTT	4799
rs776675734	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33308146	TAAATAGCCAGCTGT[A/G]GATTATATCCATAAG	4799
rs776694702	in-del	-/TTTG	0.000221223	0.0105149	intron-variant	NFX1	GRCh38.p7	9:33369890	AAAGACTGATCATTC[-/TTTG]TTTGTTTTTCAGGAA	4799
rs776713229	snp	C/T	3.29462e-05	0.00405857	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33318736	TCTCTTCAAGTATGC[C/T]ATTGCGGCAGCACCT	4799
rs776733316	snp	A/C	1.64833e-05	0.00287078	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33307206	TAGGCAAGGTAAAGA[A/C]TCCTGAGTGGAGCAG	4799
rs776778773	snp	C/T			upstream-variant-2KB	NFX1	GRCh38.p7	9:33289398	CTCCTCGAGCCCCTG[C/T]GGCACTGGCTTGGGT	4799
rs776786393	in-del	-/T			intron-variant	NFX1	GRCh38.p7	9:33356482	AGAACTCTTGTTGTC[-/T]TTTGATAAACAGAAA	4799
rs776834279	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33316726	TACTAAATGGGTTAA[A/G]GCTGGCAACAGGGTC	4799
rs776836889	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33360117	AGAATGTAAATTAGG[A/G]GTCCTAGGTATTCAG	4799
rs776862209	snp	A/G	1.68872e-05	0.00290574	missense, nc-transcript-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33351739	TGGTCACCCGTGTAT[A/G]GCACCCTGCCATACC	4799
rs776938091	snp	A/C	3.29527e-05	0.00405898	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33366679	CATGAACAGAGACCA[A/C]CGCCGGATCATCCAT	4799
rs776953622	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33347216	TCAAAGTAAATACAC[C/T]CAGAAGTAGAAGCTT	4799
rs776992796	snp	C/T	1.72582e-05	0.00293748	intron-variant	NFX1	GRCh38.p7	9:33338618	TTAGGCATAATCAGA[C/T]TCCATTCATCCAGGT	4799
rs777041406	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33345054	GTAATCTCAGCTACT[C/T]AGGAGGCTGAGGCAG	4799
rs777106920	snp	C/T	1.65023e-05	0.00287244	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33311128	CATCCAGGACCCTGC[C/T]CACCCTGCCCTGCCT	4799
rs777143618	snp	C/T			utr-variant-3-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33370054	CAGATAAATCATGCC[C/T]GTTCCCCTCTGCCTG	4799
rs777199700	snp	C/G	0.000148472	0.00861475	utr-variant-5-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33290548	GACTTGGCTGTACAG[C/G]TCGATCTAGGTTCTG	4799
rs777224783	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33360833	GTGTCTTTTGAAAAA[C/T]TGGAAATCTAGCAGT	4799
rs777228386	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33316939	ATTCATTACCTCTGT[A/G]AAAAGCCTTTGTTCT	4799
rs777233202	snp	A/T	3.29701e-05	0.00406005	intron-variant	NFX1	GRCh38.p7	9:33338496	TTTTTTTTCTTTTTA[A/T]TTTGCCACAGCAGAT	4799
rs777289568	snp	C/T	1.65515e-05	0.00287671	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33290593	GGAGGCGCCTCCTGT[C/T]TCAGGTATTGTCCCG	4799
rs777291826	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33315430	AGCCAAAATCTGCTT[C/T]CCTGAAATATACTCT	4799
rs777295586	snp	A/G	0.0025641	0.0357138	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33364824	AAGGCCAGCTTGATG[A/G]AAAAAAAAAAGCAAT	4799
rs777313911	snp	A/G	3.02375e-05	0.00388817	intron-variant	NFX1	GRCh38.p7	9:33342883	CTGTATAGTTTATTA[A/G]AAGAGTTTTTTAGAA	4799
rs777322745	in-del	-/T			intron-variant	NFX1	GRCh38.p7	9:33302088	ACAAACAAAAAAACA[-/T]TTTTTTTTTCATTTT	4799
rs777322909	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33306406	AGCAGACATTTGGAC[A/C]TATGGGTCTGAAACT	4799
rs777327879	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33339661	AAGTCTCATCCAAGA[C/T]AAGGCAAGTCGCTTT	4799
rs777353252	in-del	-/TT			intron-variant	NFX1	GRCh38.p7	9:33331694	AACTTCAGTAGCTGC[-/TT]TTTTTTTTTTTTTTT	4799
rs777356361	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33361640	TAGCTGGGCATGGTT[A/G]CGGGCGCCTGTAATC	4799
rs777358299	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33338917	TTGTGTGTTGTCCCA[A/G]CACAAACTGGCCTGG	4799
rs777376611	snp	A/G	1.64982e-05	0.00287208	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33295086	GAGTATTGGATGGGT[A/G]TGGAGCCAGACGAAA	4799
rs777376924	snp	C/T	1.67486e-05	0.00289379	intron-variant	NFX1	GRCh38.p7	9:33313842	TGTTCTTTTCTGGAA[C/T]CTTATTAATGATTGT	4799
rs777390241	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33293659	TGTCCTTAGGCAAAC[C/T]ATTTTGTCTTTGTGC	4799
rs777391776	snp	C/T	3.29582e-05	0.00405931	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33294553	CAGTTCACCACCTCC[C/T]TGTCACCTTTCCAGG	4799
rs777410050	in-del	-/CTGTT			intron-variant	NFX1	GRCh38.p7	9:33303454	TGTGCTCCTGGCAAG[-/CTGTT]CTGGAGATGGCCAAC	4799
rs777445030	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33306085	GTATTGGAGCAAAAA[A/T]GCACAGAGGCAGGGA	4799
rs777449193	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33292610	GCCAGTTTCCTGATC[A/G]ATGTGTCCTGTTTCC	4799
rs777452439	in-del	-/T	1.65033e-05	0.00287252	intron-variant	NFX1	GRCh38.p7	9:33367476	CATCTCCACAAACAA[-/T]TCTCACTTTTCAATG	4799
rs777455055	in-del	-/AT			intron-variant	NFX1	GRCh38.p7	9:33361796	ACTCCATCTCCAAAA[-/AT]ATATATATATATACA	4799
rs777476642	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33314341	TAACTGCTTGAAAAG[A/G]ACCAGATTATTATGG	4799
rs777498537	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33305069	GTTCTTCCAGGGGAC[C/T]ATTAATTTAACATGT	4799
rs777612672	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33290996	GGAGTGGTGGCGTGG[C/G]CGCGAGCCGAATTCC	4799
rs777646204	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33327610	GACCTCATGATCTGC[A/C]CACCTCGGTCTCCCA	4799
rs777673435	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33299600	TGCTGAGGTGGGAGG[A/G]TCGCTTGGGCCCAGG	4799
rs777681699	snp	A/G	1.64904e-05	0.00287139	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33366638	ATACAGGGAAAGAAT[A/G]GTAAGAAAAGCCACA	4799
rs777717084	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33317695	AGAGTCTTAATTATG[A/G]CCGGGCGTGGTGGCT	4799
rs777724789	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33313189	TCATGGAACTCAGAG[A/G]TGAAATCACATAAAG	4799
rs777764187	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33360539	CCCTTACTGGATAGA[A/G]TCTTTCATAAATACA	4799
rs777770472	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33298243	GACATTTGAACAGAG[A/G]CAAGAATGAAGTACA	4799
rs777785376	snp	A/G	1.65162e-05	0.00287365	intron-variant	NFX1	GRCh38.p7	9:33307183	TGACTCTCTGATCTG[A/G]TATGTTCTAGGCAAG	4799
rs777804825	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33346125	CTTGGGGATCTTAGG[A/G]TAGCCCTCCCAGCGT	4799
rs777819227	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33359456	ATACAAAAATTAGCC[A/G]GGCATGGTGGCAGAC	4799
rs777820194	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33321244	CAGTAACAGACCTTG[A/G]GATGGGACAAGACCA	4799
rs777820463	in-del	-/AATA			intron-variant	NFX1	GRCh38.p7	9:33323451	CTGTAGGATAATCAT[-/AATA]AATATGTTCAAAGAA	4799
rs777825964	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33307725	GTCTGGGGAAAGACA[A/G]TTGTTTAGGGTCCCG	4799
rs777833367	snp	C/G	1.64751e-05	0.00287007	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33328638	GTGGACCATGCTCTC[C/G]CACATCAGTTATTTC	4799
rs777875367	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33333919	GGAGGCCAAGGTGGG[C/T]GGATCACCTGAGGTC	4799
rs777875408	snp	A/G	1.65307e-05	0.0028749	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33294679	TCCTTGTAATAAATC[A/G]CCCAAGAGCCATGGC	4799
rs777881189	snp	C/T	3.72045e-05	0.00431287	utr-variant-3-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33370016	AAAAGAATGATTAGG[C/T]ATAGTGGAGACTTAT	4799
rs777884767	snp	A/C	1.66863e-05	0.0028884	missense, nc-transcript-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33351720	CCACCCCCAGAGCTG[A/C]CTGTGGTCACCCGTG	4799
rs777891978	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33368393	GATTTAAAGAGAAAA[C/G]AAAACCAAGTTGGCA	4799
rs777898995	snp	C/G	9.88614e-05	0.00703	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33301390	TTTGAACTGCATAAA[C/G]AAATGGGCAAGGTCT	4799
rs777958892	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33322654	AGAGGTTCCACTGAG[A/T]GAAGCAAGCCAAGAA	4799
rs777959054	snp	C/G	1.67435e-05	0.00289335	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33364024	GGAGATTAGCAGAGG[C/G]ATTTCATATCAGTGA	4799
rs778009699	snp	G/T	1.67652e-05	0.00289522	intron-variant	NFX1	GRCh38.p7	9:33354930	TTAATCTCCTTGCCC[G/T]TGAGCTCTGTGAAAT	4799
rs778018133	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33335056	CTCAAATATCATTTC[A/T]CCCATAAATACTTCA	4799
rs778018873	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33325528	AATTAGCCGGGCATG[A/G]TGGCGGGCACCTGTA	4799
rs778019831	snp	A/C	1.65787e-05	0.00287907	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33294793	CTCAGATACAGCTGG[A/C]TTAGAGAGCTCGACC	4799
rs778040594	snp	A/G	1.64743e-05	0.00287	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33344175	CGCTAGAGTCCATGA[A/G]TGTGACCATCCAGGT	4799
rs778073373	snp	C/G	3.32237e-05	0.00407563	intron-variant	NFX1	GRCh38.p7	9:33307350	TGGACATGCTTTGCT[C/G]GTGGCTCTAAGTAAA	4799
rs778130319	snp	A/T	1.64727e-05	0.00286986	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33318796	GGAAAGTCTGATGGA[A/T]TTGGGGATTTCAGCT	4799
rs778150191	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33355243	TACATATTGAAGATT[G/T]GAAGTGTGCAGATCA	4799
rs778162686	snp	A/G	1.6476e-05	0.00287014	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33318934	ATGCGGTAACCATAC[A/G]TGTTCGCAAGTGTGC	4799
rs778195126	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33308707	GAAAATTAAATGAAT[C/T]AGTGCATCTATGCGG	4799
rs778261791	in-del	-/A	3.32099e-05	0.00407478	intron-variant	NFX1	GRCh38.p7	9:33301466	TCTCCCCTATTTGAT[-/A]ACGTTTAAGTATTAT	4799
rs778272099	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33331112	TGGAGCTTGCAGTGA[A/C]CCGAGATTGCACCAC	4799
rs778350965	snp	C/G	1.7221e-05	0.00293432	intron-variant	NFX1	GRCh38.p7	9:33366793	GGTCAATCCCGCCGT[C/G]AGAGGAAGAACTCCT	4799
rs778382118	in-del	-/TC			intron-variant	NFX1	GRCh38.p7	9:33342118	GAGACCCTGTCTCTG[-/TC]TCTCTCTCTCACACA	4799
rs778385108	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33311955	CCTAGCACAGTATCT[A/G]GCATCTAAGAGTCTT	4799
rs778396783	snp	A/T	7.05206e-05	0.00593762	intron-variant	NFX1	GRCh38.p7	9:33301245	TTAATCTTTTTTGTT[A/T]TTTTGTTTTTTAAAC	4799
rs778399234	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33308970	TGGGCAGTCAGATAC[C/T]TCATTCCCTTTGACT	4799
rs778403045	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33341027	CAACATCTGCCTGTT[A/G]CCCAGTTCCAAAGTC	4799
rs778513685	snp	C/G	1.91046e-05	0.00309062	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33342762	ATAAGGAGCACAAGT[C/G]TCCTTTGATTTGTGG	4799
rs778517492	snp	A/C			intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33350149	TCTCTACTAAAAATA[A/C]AAAAATTAGCTGGGC	4799
rs778540604	snp	A/G			intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33366306	CTTTAGTCATTTTTG[A/G]GGAATATCACCCACT	4799
rs778569524	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33313068	GGGTACATGATAGCT[G/T]TCCTCCCGTCTGTAA	4799
rs778619591	snp	A/C	3.30682e-05	0.00406608	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33290588	ATGGCGGAGGCGCCT[A/C]CTGTCTCAGGTATTG	4799
rs778622587	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33326121	AGTGGTAAATTTTGT[A/G]TAAGAGGGGGGCTAG	4799
rs778643902	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33318170	ATCATTAGATCTTAT[A/C]CTCTCATGCCAATTT	4799
rs778679819	snp	A/G	6.59131e-05	0.0057404	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33295202	GAGGGCCACCGACAT[A/G]CAAACGCAGGACACA	4799
rs778698408	in-del	-/T	5.00551e-05	0.0050025	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33364834	GATGAAAAAAAAAAA[-/T]GCAATCAAGTCCTGG	4799
rs778702049	snp	A/T	1.64819e-05	0.00287066	missense, nc-transcript-variant	NFX1, LOC105376018	GRCh38.p7	9:33351594	GTCACCTGGTTGATA[A/T]CTCTTGCGGATTACC	4799
rs778709362	snp	A/G	1.81965e-05	0.00301628			GRCh38.p7	9:33294420	TTTTTTATGTCCTAG[A/G]TACTTTTAAATTCAA	4799
rs778787960	snp	G/T	1.70174e-05	0.00291692	intron-variant	NFX1	GRCh38.p7	9:33319147	CTAGTAAGCGTAAAG[G/T]TGGCTTTAAAAATAT	4799
rs778799184	snp	A/G	1.6477e-05	0.00287024	intron-variant	NFX1	GRCh38.p7	9:33364670	GGTTCTCAGAAGGGC[A/G]GGGACAGACAAAATT	4799
rs778819206	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33311238	CATGATTGACTTGTG[A/T]ATTTCTGAAATAAAA	4799
rs778853826	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33292463	CACCTGTTGGACACC[C/T]ACTGTGCTGCTGTGT	4799
rs778883175	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33291167	CCCCCTCCTGGAGTT[A/G]CCTCAGTGTGTAGAG	4799
rs778890382	in-del	-/T			intron-variant	NFX1	GRCh38.p7	9:33301827	CTGTAATCCCAGCGC[-/T]TTGGGAGGCCAAGGC	4799
rs778954976	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33321041	AAATGTGTTTATGAT[A/G]TGGAGATCAAATGAC	4799
rs778955600	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33332792	TGAAAAAATATGTTA[A/G]TGGTAGAATCTAGAT	4799
rs778956660	snp	A/G	6.88693e-05	0.0058677	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33364784	AATAAGGTTGAAGTC[A/G]AAACATCCCACTGGA	4799
rs778970893	snp	A/C			downstream-variant-500B	NFX1	GRCh38.p7	9:33371540	AGTTTCACTGACCTC[A/C]TTAGGGTTATGAAGA	4799
rs778984860	snp	A/C			intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33366325	ATATCACCCACTCCC[A/C]AGTTATGGAACCCAT	4799
rs779028887	in-del	-/AAAG			intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33365277	GAAACTCTGTCTCAA[-/AAAG]AAAGAAAGAAAGAAA	4799
rs779078004	snp	C/G	0.000197746	0.00994152	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294596	GATGAAATCTCTGCT[C/G]TTCATCAGCATAGTT	4799
rs779126884	snp	A/C	4.94214e-05	0.00497074	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33303237	TCAGAATGTTTCTGC[A/C]CATGTTCCTAATACC	4799
rs779130162	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33344390	TTGGTTTACTCTAGG[G/T]ATGTCAAACACACCT	4799
rs779151490	snp	G/T	1.79435e-05	0.00299523	intron-variant	NFX1	GRCh38.p7	9:33369896	TGATCATTCTTTGTT[G/T]GTTTTTCAGGAATCC	4799
rs779159795	snp	C/T	4.96257e-05	0.004981	intron-variant	NFX1	GRCh38.p7	9:33307172	GTTTGTACCATTGAC[C/T]CTCTGATCTGATATG	4799
rs779165109	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33300921	GATTTAGAGGATCCT[G/T]GAAAATAGAAAATGC	4799
rs779203298	in-del	-/T			intron-variant	NFX1	GRCh38.p7	9:33344483	CCACTTTGGTGCATG[-/T]TTTTGAAATTTAGCA	4799
rs779218191	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33299426	ATTTGGTTAAATTTC[C/T]GTAATCCCAGTACTT	4799
rs779245404	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33298958	ATTTGGAAGGAAGAT[G/T]TTATGCCTGAGCAAC	4799
rs779274407	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33307542	CTCAGAAAGGCCAAG[C/T]CTCTTGCCCAGCATC	4799
rs779304552	snp	C/T	8.23906e-05	0.00641783	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33295207	CCACCGACATACAAA[C/T]GCAGGACACAGAAAC	4799
rs779327775	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33306383	TGAAACCCCAAGCAA[C/G]AATGTTCAGCAGACA	4799
rs779333340	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33329529	GGCTTAGAGATTACC[C/T]CTCAGAAGCCAAGCA	4799
rs779359597	snp	C/T	1.64754e-05	0.00287009	intron-variant	NFX1	GRCh38.p7	9:33344022	GTATGTACTTGCACA[C/T]CCCAAACTCAGAAAG	4799
rs779393131	snp	C/T	0.000164775	0.00907525	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33366656	AAGAAAAGCCACAGC[C/T]TCCCTCCCATGAACA	4799
rs779432093	in-del	-/C			intron-variant	NFX1	GRCh38.p7	9:33355803	GTGTGTACCACCATG[-/C]CCAGCTGATTTTTGT	4799
rs779488966	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33341270	GATGGCAGCAGGCAG[A/C]GGGAGAGAGCTTGTG	4799
rs779531641	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33302826	AGGCGCGCACCACCA[C/T]GCCCAGCTAATTTTT	4799
rs779535393	snp	A/C	1.65217e-05	0.00287412	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33290580	GGCACGGGATGGCGG[A/C]GGCGCCTCCTGTCTC	4799
rs779557457	snp	G/T	3.41e-05	0.00412902	intron-variant	NFX1	GRCh38.p7	9:33338480	TATCCTTTGTCTGGT[G/T]TTTTTTTTCTTTTTA	4799
rs779559940	in-del	-/ACGCT	1.64789e-05	0.0028704	frameshift-variant, nc-transcript-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33351620	TTACCCTGCAGTGCC[-/ACGCT]ACCATGTGGGATGCA	4799
rs779568439	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33314543	TTAACTGGGCGTGGT[G/T]GTGGGCGCCTGTAAT	4799
rs779584046	snp	A/C	9.579e-05	0.00691996	intron-variant	NFX1	GRCh38.p7	9:33301228	GGTTTTTTGTGTTTG[A/C]GTTAATCTTTTTTGT	4799
rs779591254	snp	C/T	1.6473e-05	0.00286988	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33344156	CTGAATGTACCCAAA[C/T]CTGCGCTAGAGTCCA	4799
rs779592892	snp	A/G	1.64895e-05	0.00287132	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33366722	GTTTATGGCCTGGAG[A/G]GCGTGAGCTATGACA	4799
rs779645956	snp	C/G	1.65751e-05	0.00287876	intron-variant	NFX1	GRCh38.p7	9:33311086	GCTGTGGTTTATTCA[C/G]TGAAACCTTTCTCTT	4799
rs779648057	snp	A/G	1.80325e-05	0.00300265	utr-variant-3-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33369998	ATCATGATGCACTTA[A/G]ATAAAAGAATGATTA	4799
rs779663091	snp	G/T	1.64792e-05	0.00287042	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352637	CGTTCCATGTTCATC[G/T]GACTTCAGGTAGAGC	4799
rs779665984	in-del	-/A			intron-variant	NFX1	GRCh38.p7	9:33321168	TGTTGGTGATGAGAG[-/A]AGAAGGAAATGTGAA	4799
rs779680360	snp	A/C/T	3.29773e-05	0.00406051	synonymous-codon, stop-gained, nc-transcript-variant	NFX1	GRCh38.p7	9:33295382	GTATCTCCTTTCTCC[A/C/T]GAGGCAAACAGAACC	4799
rs779723334	in-del	-/T			intron-variant	NFX1	GRCh38.p7	9:33334579	ATAGTAGTTTGTTAG[-/T]TAGGGTTTCAGATCT	4799
rs779772179	snp	A/G	1.64895e-05	0.00287132	utr-variant-5-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33290530	TGACCTGGTGACAGT[A/G]CTGACTTGGCTGTAC	4799
rs779772284	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33328176	TCACCACTCCTGGCT[A/G]ATTTCTTGTTTTTGT	4799
rs779802656	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33343548	TGTTTTCAAATAATT[A/G]TTGATATTCTTTGAA	4799
rs779816614	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33329583	AAGGTTTAATTCTTC[A/G]CTGTACATCTGTTTT	4799
rs779827679	snp	A/G	3.335e-05	0.00408337	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33338568	GTGTGGACGGCATAA[A/G]TGTAATGAGATATGC	4799
rs779846418	snp	A/G	1.75225e-05	0.00295989	intron-variant	NFX1	GRCh38.p7	9:33364159	TTGTCAGGGTGTTTG[A/G]TCTTTTGAGATGTCA	4799
rs779867888	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33342996	TTGAGACTTTTTTTA[A/T]AGTTACTTCTAATGC	4799
rs779934301	snp	C/T	0.000478583	0.0154617	intron-variant, utr-variant-3-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33347756	CAGCACAATTCACAA[C/T]TGCAAAAATGTGGAA	4799
rs779978109	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33309832	CTCCAGGCACTTCCA[A/G]TATATAGCCAGTGTT	4799
rs779986710	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33303870	ATGACTAACTTCCCT[C/G]TAGTTGTTGATTTTT	4799
rs779997334	snp	C/T			intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33366426	GCGACTGTTGTGGCT[C/T]ACAGAGTAGGTGAAA	4799
rs780044199	snp	C/G			intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33349988	CTCCAGCCTAGGCAA[C/G]AGAGCAAGATTCTGC	4799
rs780062519	snp	C/G	8.23947e-05	0.00641799	intron-variant	NFX1	GRCh38.p7	9:33311195	AAAGTTAAAATTACA[C/G]CCTAAAGAAGACCTC	4799
rs780079708	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33294390	TGAAGTTTAATCTCT[C/T]TACTGGCATGTCTAT	4799
rs780083768	snp	A/G	1.65737e-05	0.00287864	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33364057	ATTCTGATCCTTTCA[A/G]TATACGTTCTTCAGG	4799
rs780176698	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33305417	GATTCATCCACTTAC[A/G]GAGCCCAGGATCTAT	4799
rs780181886	snp	A/C			intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33349719	CCCTGTTGTCTCTTA[A/C]TTTTTTAAAGGACAG	4799
rs780219736	snp	A/G	1.65149e-05	0.00287353	intron-variant	NFX1	GRCh38.p7	9:33301430	CAAGCAGGTCAATTA[A/G]TTCTCTCTTCTGAGT	4799
rs780328531	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33305265	AGCTGGATGATTAAG[A/G]GAAGCCTTCTTGGAG	4799
rs780332636	in-del	-/TTT			intron-variant	NFX1	GRCh38.p7	9:33302358	TTCTATCTAACTGTA[-/TTT]TTTTTTTTTTTTTTT	4799
rs780336420	snp	C/T	1.65141e-05	0.00287346	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33295056	CTGACTCTTCAGAGG[C/T]ATCCTCTAGAAAAGG	4799
rs780336859	snp	C/T	1.9623e-05	0.00313227	intron-variant	NFX1	GRCh38.p7	9:33369864	CCTGTATCTGTTTCC[C/T]CCAAAGAAGAAAAGA	4799
rs780345629	snp	C/T			downstream-variant-500B	NFX1	GRCh38.p7	9:33371406	ATCTGTTACCTCTTT[C/T]AAGCAGTGGGTTCAG	4799
rs780351763	snp	C/G	1.64966e-05	0.00287194	missense, nc-transcript-variant	NFX1, LOC105376018	GRCh38.p7	9:33351574	GTTTCGGAGCAACAT[C/G]CCCTGTCACCTGGTT	4799
rs780383710	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33319671	CACACCACCACGCCC[A/G]GCTAATTTTTGTATT	4799
rs780439321	snp	C/T	3.29554e-05	0.00405914	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294575	CTTTCCAGGCAGGTC[C/T]CTTATGATGAAATCT	4799
rs780462813	snp	C/T	1.64749e-05	0.00287005	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33303213	GAGTGGTTGGAGGTG[C/T]CCTGCCTGTCAGAAT	4799
rs780497285	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33333250	ATAAAAGGTCTTACT[A/G]TAGTCAGAAAGAAAG	4799
rs780512027	snp	A/G	1.88049e-05	0.00306629	intron-variant	NFX1	GRCh38.p7	9:33354079	CCCTTTCTTTTTTAT[A/G]TTTCAGAATAGCTGC	4799
rs780513290	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33320810	TTGTGAGGTAAAGCT[A/G]GAATCTTTAGGTTTG	4799
rs780568457	snp	C/T	3.30213e-05	0.00406319	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294648	CTAAGAGTCAGCAGA[C/T]GTCTTTCCAGTCCTC	4799
rs780604454	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33327967	GGGAGATTCAAGTCT[A/G]CACTGGAGATGTGGG	4799
rs780620519	snp	C/T	3.29641e-05	0.00405968	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352627	TGCTAAAAGTCGTTC[C/T]ATGTTCATCTGACTT	4799
rs780659745	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33341056	TCACTTCCACATTTT[C/T]GGGTATCTTTTCAGC	4799
rs780687870	snp	C/T			intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33365976	AAGCCCCCAGCGCTG[C/T]ATTGGCTTCCTCCCC	4799
rs780696575	snp	A/C/T	0.000336873	0.0129741	missense, nc-transcript-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33351729	GAGCTGACTGTGGTC[A/C/T]CCCGTGTATGGCACC	4799
rs780729254	snp	A/C	4.94173e-05	0.00497053	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33318771	AGATGTGTTATGTGG[A/C]ACCGATGTAGGAAAG	4799
rs780741203	snp	A/G	1.82035e-05	0.00301686	intron-variant	NFX1	GRCh38.p7	9:33354191	TCATCAAGCCAGGTA[A/G]TTTTTAAAATGCATA	4799
rs780742916	snp	A/G	3.53388e-05	0.00420335	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33342805	TTGTGGCCTTCATAG[A/G]TGTGAAGAACCTTGT	4799
rs780770751	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33358995	TGAGCCACCACACCC[A/G]GCCTAAATTGGTATT	4799
rs780781378	snp	C/G	1.64882e-05	0.00287121	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33366643	GGGAAAGAATAGTAA[C/G]AAAAGCCACAGCTTC	4799
rs780823681	snp	C/T	1.64885e-05	0.00287123	intron-variant	NFX1	GRCh38.p7	9:33318686	TGACATTTTAAGAAC[C/T]CATACATGTTACTAA	4799
rs780835560	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33315569	GCTTCATTTCTTCCC[G/T]GTGAAACATGCTCAG	4799
rs780858582	in-del	-/AA			upstream-variant-2KB	NFX1	GRCh38.p7	9:33290001	AATAAACGCCTTTGT[-/AA]AAAAAAAAAAAAAAA	4799
rs780876090	snp	A/C			missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294942	ATGGTAGAGGACCAA[A/C]AGTCAAGGGGAAACT	4799
rs780899318	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33340011	TGGCTTTTCCAGGCA[C/T]ACAGTGCAAGCTGTC	4799
rs780911637	snp	A/G	1.64776e-05	0.00287028	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33295244	GGCCCCATTCCAAAG[A/G]ATGACCTCAATGAAA	4799
rs780913690	in-del	-/TTC			intron-variant	NFX1	GRCh38.p7	9:33345387	AGGCTGAGGCAAGAG[-/TTC]AATCACTTGAACCCG	4799
rs780931078	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33293890	AAATTTCTCAGTAAC[C/T]GTTGAAATAAGTATT	4799
rs780936274	in-del	-/AAAGA			intron-variant	NFX1	GRCh38.p7	9:33317441	AAAAAAAAAAGAAAG[-/AAAGA]AAAGAAAAGAAATTG	4799
rs780977047	snp	A/G	1.89658e-05	0.00307937	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33351797	AAAGCTAAGGTGGGT[A/G]TTTCTGGCCACAGAT	4799
rs780991839	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33302482	TCCTCCTGCCTCAGA[C/T]TCCCAAGCAGCTGAG	4799
rs780994575	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33353798	GGTTCAAGTGATTCT[C/G]CTGCTTCAGCCTCCT	4799
rs781022787	snp	A/G	3.29761e-05	0.00406041	utr-variant-5-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33290522	GGGGCACGTGACCTG[A/G]TGACAGTGCTGACTT	4799
rs781104327	snp	A/G	1.6782e-05	0.00289668	intron-variant	NFX1	GRCh38.p7	9:33354941	GCCCTTGAGCTCTGT[A/G]AAATTAATGGGAGGG	4799
rs781125716	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33310762	GCCATTCTGCCTTTT[A/C]CCTGAGTAGCAAACT	4799
rs781137522	in-del	-/T			frameshift-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33344163	TACCCAAACCTGCGC[-/T]AGAGTCCATGAGTGT	4799
rs781192765	snp	G/T	1.66291e-05	0.00288345	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33364037	GGCATTTCATATCAG[G/T]GAGGATTCTGATCCT	4799
rs781197229	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33335322	TGCAACCTCCACCTC[C/G]TGGGCTCAAGCAATT	4799
rs781216596	snp	A/G	1.65321e-05	0.00287502	intron-variant	NFX1	GRCh38.p7	9:33338464	GTTGTATGAATGTTC[A/G]TATCCTTTGTCTGGT	4799
rs781230023	in-del	-/TTACTACAAGGAGG			intron-variant	NFX1	GRCh38.p7	9:33329072	CTCATGGTTAGAGCT[-/TTACTACAAGGAGG]TTACAGTTTTATTAC	4799
rs781231656	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33325066	GGAATATGAGGAGGA[G/T]AGTAGAAAGAAGTGG	4799
rs781244429	snp	A/G	1.65869e-05	0.00287979	intron-variant	NFX1	GRCh38.p7	9:33311064	TTTGTTCGGGTTTGG[A/G]TACATGGCTGTGGTT	4799
rs781250124	snp	A/G			intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352885	CAGATACATGTGTTT[A/G]TCATAGTATCCTTGC	4799
rs781283259	in-del	-/G			intron-variant	NFX1	GRCh38.p7	9:33321565	AAGCAAACAAAGCTA[-/G]GGGAAAACTATAAAA	4799
rs781289066	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33368678	GGAGAGGGGTGCCTA[C/T]TCCTGTTCTGGCTTT	4799
rs781330477	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33296627	GTAGTCCCAGACACT[C/T]AGGAAGCTGAAGTGA	4799
rs781373695	snp	C/T	0.000282048	0.011872	intron-variant, synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33347728	AAAGATACCTGCACA[C/T]GCATGTTTATAGCAG	4799
rs781379316	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33309493	CCTTAAAACCTGCTC[C/T]TGCTCTTTTGTGGCT	4799
rs781424720	snp	A/G	3.29609e-05	0.00405948	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33347065	GTCATAGTGAGGAGA[A/G]GTGTCCCCCTTGCAC	4799
rs781447908	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33318335	CAGCTTAGCTTGTCT[A/G]TCTCCTGTAACATCA	4799
rs781456935	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33369804	ATAAAATAAATGTTT[A/T]AGATTCACAAATGGT	4799
rs781476573	snp	A/T	1.64743e-05	0.00287	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33319051	AGAACTTGGAAGTAG[A/T]AGTCGGAAAACATGC	4799
rs781481080	snp	A/G	3.29544e-05	0.00405908	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33311171	CATGTGAATGTGGAC[A/G]AACCAGGTAAAGTTA	4799
rs781481115	snp	C/T	1.65778e-05	0.002879	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294804	CTGGATTAGAGAGCT[C/T]GACCAGATCAGAGAG	4799
rs781492768	in-del	-/CAG	1.65605e-05	0.0028775	intron-variant	NFX1	GRCh38.p7	9:33313811	AAGTGGTGGGCACAC[-/CAG]CTAGCAATGCTTGTG	4799
rs781569062	snp	A/G	1.65244e-05	0.00287436	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294972	TCAAATGTGAATGGA[A/G]TAACCGAACAACTCC	4799
rs781577269	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33336577	CTACCACATGATGTG[A/G]TGTCTCTGATATCTC	4799
rs781590864	snp	C/G/T	4.94485e-05	0.00497214	missense, nc-transcript-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352710	CTGAAGCATCTAGTA[C/G/T]TTATCAAAGGTTAGT	4799
rs781606378	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33319608	TCTGACTCCTGGGCT[C/T]AAATGATTCTTGTGT	4799
rs781641100	in-del	-/CAA			intron-variant	NFX1	GRCh38.p7	9:33308254	CTAGACCAGACTAGG[-/CAA]CAAAATGAGACCCCG	4799
rs781647506	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33332164	TTTCCTTTGCATGCC[C/T]TTAGCAGCCCTCTTT	4799
rs781665875	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33364492	TCCTGGAGTCCCTGG[A/C]CTTTCAGTGGCTACT	4799
rs781670847	snp	A/T	1.64866e-05	0.00287106	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33301288	TGAACAACTAACAAC[A/T]GAAAAATACGAGTGC	4799
rs781695236	snp	C/T	1.64798e-05	0.00287047	intron-variant	NFX1	GRCh38.p7	9:33303175	TTATTTGGCCTACTC[C/T]CATTTTTCCTGACAG	4799
rs781710180	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33305706	AGTAGGAATGGGAGT[C/T]ACCCAAAGTTTCATG	4799
rs781715242	snp	C/T	6.28062e-05	0.00560349	intron-variant	NFX1	GRCh38.p7	9:33354068	TGCCTCTTTTTCCCT[C/T]TCTTTTTTATATTTC	4799
rs781749963	snp	C/T	1.64732e-05	0.0028699	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33367568	TGCTTGAAAGGGAAA[C/T]GCAGGCACGGCCTCC	4799
rs781756626	in-del	-/GCTTTATTTA	3.31274e-05	0.00406972	intron-variant	NFX1	GRCh38.p7	9:33346991	ATAATGGTTTACATG[-/GCTTTATTTA]GCTTTATTTAGAAAG	4799
rs796075790	snp	A/G			utr-variant-3-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33370979	GCTCCTTTAAGGCAG[A/G]TGCATTGATAGTTCC	4799
rs796077545	in-del	-/C			intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33366186	CTCCTAATTAAGAAA[-/C]CCCAACAGATGTGTT	4799
rs796079212	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33311852	TACCGCGCTCGGTCG[C/G]CAAGGATTTTTTTTT	4799
rs796109164	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33299240	GATTTCACCAGTTTT[A/T]CTGCCAATGTCCTTT	4799
rs796169345	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33368274	TGAAGATGCAAGTGG[A/G]TGTGGGGGTGAGAAT	4799
rs796176134	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33314992	TTTTTAATTGTGAAT[A/T]TAAGTTTATGTTTTT	4799
rs796212929	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33291264	AAATGTGTTGGACAG[C/T]AACCAAAAGAAACAT	4799
rs796219218	snp	A/C			missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33303251	CACATGTTCCTAATA[A/C]CTACACTTGTTTCTG	4799
rs796237747	in-del	-/TT			intron-variant	NFX1	GRCh38.p7	9:33325420	TGTAATCCCAGCACT[-/TT]GAGAGGCCGAGGCGG	4799
rs796253452	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33292494	TATCTTGGATTTAGG[G/T]TACCACTTGTATTCT	4799
rs796256658	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33332927	CTCGGCTCACTGCAA[C/T]CTCCACCTCCCAGGT	4799
rs796273643	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33362695	TAAGTTCCTGTGGTT[G/T]TTTTTTTTTTTTTTT	4799
rs796293415	in-del	-/T			intron-variant	NFX1	GRCh38.p7	9:33319965	TTTTCTTTTCTTTTC[-/T]TTTTTTTTTTTTTTG	4799
rs796329827	in-del	-/TA			intron-variant, utr-variant-3-prime, splice-donor-variant	NFX1	GRCh38.p7	9:33347943	GAAAACCAAACATCG[-/TA]TATGTTCTCAATTAT	4799
rs796485970	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33317289	CCAGGTGTAGTGGCA[C/T]GCACCTGTACTCCCA	4799
rs796521735	in-del	-/A			intron-variant	NFX1	GRCh38.p7	9:33317533	TAAATTCAGCTAATT[-/A]AAAAAAAAAAAATCA	4799
rs796527293	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33328788	AGGTATGGGAAGTGG[C/T]TGTGGCACTCAAGGT	4799
rs796633244	in-del	-/TC			intron-variant	NFX1	GRCh38.p7	9:33316813	CTGCTCATATTTCTG[-/TC]TCTCGTGCCTAGGAG	4799
rs796667414	in-del	-/T			intron-variant	NFX1	GRCh38.p7	9:33331695	AACTTCAGTAGCTGC[-/T]TTTTTTTTTTTTTTC	4799
rs796690417	in-del	-/TTTT			intron-variant	NFX1	GRCh38.p7	9:33313986	CATTGTCCTATATAA[-/TTTT]TTTTTTTTTTCTTTT	4799
rs796721415	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33369152	CTCACTGCAAGCTCC[A/G]CCTCCCGGGTTCATG	4799
rs796722565	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33329324	TATTGTGCAATCATA[A/G]TTGACTGCCCATGTG	4799
rs796792172	snp	A/G			intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352361	GGGCCTAGGGCAAGT[A/G]TCTGTCTCTGATGGT	4799
rs796827414	snp	C/T			missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294557	TCACCACCTCCCTGT[C/T]ACCTTTCCAGGCAGG	4799
rs796847017	in-del	-/C			intron-variant	NFX1	GRCh38.p7	9:33335231	CTTTCTTTTTCTTTT[-/C]TTTTTTTTTTTTTTT	4799
rs796905317	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33341852	CTGGATGCGGTGGCT[C/T]ATGCCTGTAATCCCA	4799
rs796959431	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33306870	ATATCAGTTCAGAAG[A/T]CCAGTTATAGACGAC	4799

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