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
rs581880	snp	A/G	0	0	splice-acceptor-variant	NFX1	GRCh38.p7	9:33354085	CTTTTTTATATTTCA[A/G]AATAGCTGCAATCTC	4799
rs583428	snp	A/C	0.298398	0.245271	intron-variant	NFX1	GRCh38.p7	9:33315727	ACCAGTCTCTAACAA[A/C]AACAAAAAAAAAAAA	4799
rs583431	snp	A/C	0.298144	0.245321	intron-variant	NFX1	GRCh38.p7	9:33315730	AGTCTCTAACAACAA[A/C]AAAAAAAAAAAATTA	4799
rs587608	snp	C/G	0.306679	0.24349	intron-variant	NFX1	GRCh38.p7	9:33296725	AACTTTTTTCCCCCC[C/G]CAaaacagggtcttg	4799
rs588676	snp	C/T	0.0513262	0.151752	intron-variant	NFX1	GRCh38.p7	9:33333098	aacactttgggaggc[C/T]gaggcgggtggatca	4799
rs589212	snp	C/G	0.328382	0.237395	intron-variant	NFX1	GRCh38.p7	9:33334018	AGCTGGGATTACAGG[C/G]GTGCGCCACTGTACT	4799
rs589231	snp	C/T	0.35809	0.225425	intron-variant	NFX1	GRCh38.p7	9:33334008	ACAGGGGTGCGCCAC[C/T]GTACTTGGCTAATTT	4799
rs590132	snp	A/G	0.0517044	0.152246	intron-variant	NFX1	GRCh38.p7	9:33333789	CAAAAGTTTAAATAC[A/G]GTTTTGAGGCAGATA	4799
rs593495	snp	C/T	0.299916	0.244966	intron-variant	NFX1	GRCh38.p7	9:33317436	TTCttttctttcttt[C/T]ttttttttttttttt	4799
rs599279	snp	C/G	0.298905	0.24517	intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33349703	AATTGGGGGTTCTAT[C/G]CCCTGTTGTCTCTTA	4799
rs617045	snp	C/T	0.0513262	0.151752	intron-variant	NFX1	GRCh38.p7	9:33330455	CTGTTATCCTATGTA[C/T]ATTGTAATTTCTTTC	4799
rs624596	snp	A/T	0	0	intron-variant	NFX1	GRCh38.p7	9:33300061	aaaaaaaaaaatgct[A/T]taacataggtaccat	4799
rs624638	snp	A/G	0	0	intron-variant	NFX1	GRCh38.p7	9:33300033	cattttacagatgaa[A/G]aaactggcttcatgt	4799
rs626069	snp	A/G	0.4582	0.138394	intron-variant	NFX1	GRCh38.p7	9:33316108	CTTCCATCACCTATT[A/G]TGAATCCTGACCCTG	4799
rs628777	snp	C/T	0.0505692	0.150756	intron-variant	NFX1	GRCh38.p7	9:33315449	gaaaTATACTCTCTC[C/T]TTCGTCTGCCTTTCT	4799
rs636170	snp	A/G	0.49934	0.0181589	intron-variant	NFX1	GRCh38.p7	9:33330399	CAACTTTTGTAACAT[A/G]TAAATTATACTACTT	4799
rs636759	snp	A/G	0.0402882	0.136092	intron-variant	NFX1	GRCh38.p7	9:33318390	AGTGAATGGTGTTCA[A/G]CCACGGCCTTATGGA	4799
rs637628	snp	C/T	0.0166915	0.0898172	intron-variant	NFX1	GRCh38.p7	9:33338631	CCAGAAGCCCAGCAC[C/T]TGGATGAATGGAATC	4799
rs642100	snp	A/G	0.0509478	0.151255	intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33351011	tagctggtcgtggtg[A/G]tacacacctgtaacc	4799
rs642157	snp	A/T	0.295599	0.245806	intron-variant	NFX1	GRCh38.p7	9:33344254	AGCAGTGAAGACAGT[A/T]ACACAGCAGGATCCT	4799
rs650325	snp	A/G	0.0402882	0.136092	intron-variant	NFX1	GRCh38.p7	9:33301853	AACTTCTGACTTCAG[A/G]TGATCCGCCTGCCTT	4799
rs662906	snp	A/G	0.0513262	0.151752	intron-variant	NFX1	GRCh38.p7	9:33346139	GATAGCCCTCCCAGC[A/G]TAGTTTGCAAGCCCC	4799
rs667602	snp	A/G	0.472147	0.114677	intron-variant	NFX1	GRCh38.p7	9:33324244	ttacaggcgtgtgcc[A/G]ccacacccagctaat	4799
rs673955	snp	A/G	0.0513262	0.151752	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33353561	ATACTGAGGGATTGA[A/G]TCACCTCATCGCTTC	4799
rs675469	snp	A/G	0.441705	0.160466	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33353214	CGTATTACATTGTGA[A/G]ATAAGAAGGGAAGAT	4799
rs697530	snp	A/G	0.298651	0.24522	intron-variant	NFX1	GRCh38.p7	9:33317688	aaaaTCTAGAGTCTT[A/G]ATTATggccgggcgt	4799
rs706124	snp	A/G	0.0325976	0.123435	intron-variant	NFX1	GRCh38.p7	9:33292804	ATAAGATCAGTAAAG[A/G]TGTCTAGAGAAGCCT	4799
rs706125	snp	A/G	0.0341408	0.126114	intron-variant	NFX1	GRCh38.p7	9:33292932	ATGCAGAGGGTGGCA[A/G]AGGTATTCTGGAAAC	4799
rs706126	snp	C/T	0.125874	0.217008	intron-variant	NFX1	GRCh38.p7	9:33296732	CTAAAGTAACTTTTT[C/T]CCCCCCGCAaaacag	4799
rs706127	snp	C/T	0.471578	0.115772	intron-variant	NFX1	GRCh38.p7	9:33303902	GAGGGAGACAGACAG[C/T]AAAGAAACAAAATCT	4799
rs706128	snp	A/G	0.0158815	0.0876843	intron-variant	NFX1	GRCh38.p7	9:33311102	GGATGGCAGAGACTG[A/G]AAGAGAAAGGTTTCA	4799
rs706129	snp	C/T	0.328616	0.237317	intron-variant	NFX1	GRCh38.p7	9:33317177	cccatcctggcctcc[C/T]aaagtgctgggatta	4799
rs706130	snp	C/T	0.49934	0.0181589	intron-variant	NFX1	GRCh38.p7	9:33330430	TCTTTCAGGAAAAAA[C/T]CCATATATGATTACA	4799
rs706133	snp	C/T	0.298905	0.24517	intron-variant	NFX1	GRCh38.p7	9:33343051	ATCTCAGGATCACTG[C/T]TCATATCCCAAGTTT	4799
rs706134	snp	C/T	0.496382	0.0423778	intron-variant	NFX1	GRCh38.p7	9:33345618	GTAGGATCCCACTTT[C/T]ACATTGGGGAAAAAA	4799
rs830575	snp	A/G	0.29432	0.24604	intron-variant	NFX1	GRCh38.p7	9:33291522	CCCCAACGGCTGGTC[A/G]GGGACAGAGCTGAGA	4799
rs830576	snp	C/T	0.272117	0.249026	utr-variant-5-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33290534	AGCTGTACAGCCAAG[C/T]CAGCACTGTCACCAG	4799
rs830577	snp	A/C	0.294576	0.245994	upstream-variant-2KB	NFX1	GRCh38.p7	9:33288612	AGAGAGGAATGGTAA[A/C]AGAGAAAATTCTGCA	4799
rs830578	snp	A/G	0.32885	0.23724	intron-variant	NFX1	GRCh38.p7	9:33337651	acctcgaattcctgc[A/G]ctcaaatgagcctcc	4799
rs830579	snp	C/T	0	0	intron-variant	NFX1	GRCh38.p7	9:33325521	gcccgccaccatgcc[C/T]ggctaattttttgta	4799
rs830580	snp	C/G	0	0	intron-variant	NFX1	GRCh38.p7	9:33325468	caccgtgttagccag[C/G]atggtctcgatctcc	4799
rs831264	snp	C/T	0.468249	0.121932	intron-variant	NFX1	GRCh38.p7	9:33362623	tctcctcaacctccc[C/T]tttccaccctgtccc	4799
rs831265	snp	A/T	0.298651	0.24522	intron-variant	NFX1	GRCh38.p7	9:33362101	tgggtctggctcttg[A/T]tgcccaggctggagt	4799
rs831266	snp	A/G	0.32955	0.237006	intron-variant	NFX1	GRCh38.p7	9:33359577	gagtcttgctgtatc[A/G]tctaggctagagtgt	4799
rs831267	snp	A/C	0.465263	0.127129	intron-variant	NFX1	GRCh38.p7	9:33334835	TCCTGCttattaata[A/C]tggggaaaaactgga	4799
rs831277	snp	A/T	0.29789	0.24537	intron-variant	NFX1	GRCh38.p7	9:33314975	TTCACAATTAAAAAA[A/T]TTTTTTCTATTCATG	4799
rs831287	snp	A/G	0.320335	0.239902	intron-variant	NFX1	GRCh38.p7	9:33294093	GCTAACAGTTCAGGG[A/G]TATCAATCATCAGGT	4799
rs831288	snp	C/G	0.0325976	0.123435	intron-variant	NFX1	GRCh38.p7	9:33293885	TTATTTCAACGGTTA[C/G]TGAGAAATTTAAATA	4799
rs844216	snp	C/T	0.298398	0.245271	intron-variant	NFX1	GRCh38.p7	9:33336717	gctatttgggaggct[C/T]gtgtgggaggaccac	4799
rs844217	snp	A/G	0	0	intron-variant	NFX1	GRCh38.p7	9:33325479	agacagggtttcacc[A/G]tgttagccagcatgg	4799
rs844238	snp	A/T	0.0345262	0.126772	intron-variant	NFX1	GRCh38.p7	9:33362630	accaacctctcctca[A/T]cctcccttttccacc	4799
rs854169	snp	A/G	0	0	intron-variant	NFX1	GRCh38.p7	9:33355829	tttgtatttttagta[A/G]aaatggggtttcacc	4799
rs854170	snp	A/G	0	0	intron-variant	NFX1	GRCh38.p7	9:33355947	accacgcccagccca[A/G]aacattcttaaactt	4799
rs863816	snp	A/G	0	0	intron-variant	NFX1	GRCh38.p7	9:33325401	gctgggattacaggc[A/G]tgagccaccgcgccc	4799
rs1070046	snp	A/C	0.0402882	0.136092	intron-variant	NFX1	GRCh38.p7	9:33323668	tgaggcaggagaatc[A/C]cttgaacccaggagg	4799
rs1070047	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33323492	aggcatggtggctca[C/T]gcctgtaatcccagc	4799
rs1096495	snp	C/T	0.465158	0.127307	intron-variant	NFX1	GRCh38.p7	9:33334218	ATCCCCCAGCCCTGG[C/T]CTCCCAAAGCATAAG	4799
rs1103478	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33326392	cacttcagcctgggc[A/G]acagagcaagcctct	4799
rs1198239	snp	A/G	0.313082	0.241911	intron-variant	NFX1	GRCh38.p7	9:33358135	tctgtctcaaaaaaa[A/G]aaTTACaagtaatac	4799
rs1198251	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33357007	catgcccggctTAtt[A/T]ttttttttttttttt	4799
rs1702623	snp	C/G	0	0	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33351867	GAACTGTCTACAGTG[C/G]CCCCTGGGCATGCAT	4799
rs1702963	snp	A/G	0.295854	0.245759	upstream-variant-2KB	NFX1	GRCh38.p7	9:33289508	CACCCCCTGCCCGAC[A/G]CTTCTCCCCACCCCC	4799
rs1971352	snp	A/G	0.124144	0.21601	intron-variant	NFX1	GRCh38.p7	9:33318104	TATTTTATTTTTATT[A/G]TATATGTGATTTTAA	4799
rs2230122	snp	A/G	0.134544	0.221743	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33369945	GAAAATAACCAAGGA[A/G]CCAATAATTGACTAT	4799
rs2274866	snp	G/T	0.00161325	0.0283553	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33367586	TGATGAGGAATCGGT[G/T]GTGGAGGCCGTGCCT	4799
rs2292243	snp	C/T	0.207559	0.246371	intron-variant	NFX1	GRCh38.p7	9:33328814	TGCCTTATCCCACTA[C/T]AGGCCTCTGGACCTT	4799
rs2485447	snp	G/T	0	0	intron-variant	NFX1	GRCh38.p7	9:33290603	CCTGTCTCAGGTATT[G/T]TCCCGGCCCGAGCGG	4799
rs2661052	snp	A/G	0.472241	0.114494	intron-variant	NFX1	GRCh38.p7	9:33301851	CTTCTGACTTCAGAT[A/G]ATCCGCCTGCCTTGG	4799
rs2860036	snp	A/G	0.0141037	0.0827824	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33344122	GCCTAGTACCACAGG[A/G]AACTGGAGGGTAAAT	4799
rs2940425	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33307800	AAAAAAAAAAAAAAA[A/G]AAAGAAAGAAAGAAA	4799
rs2993125	snp	C/T	0.0509478	0.151255	intron-variant	NFX1	GRCh38.p7	9:33308072	AGCCTCCCAACATGC[C/T]AGGATTACTGGTGTG	4799
rs3739676	snp	A/G	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33346871	TTGCTTTATGTTAAA[A/G]TGTTGAAGGACAAGC	4799
rs3814515	snp	C/T	0.0991586	0.199366	intron-variant	NFX1	GRCh38.p7	9:33290659	GAGGCCCTAGAACTT[C/T]GTCACTGACCCAATT	4799
rs3849903	snp	A/G	0.49334	0.057322	intron-variant	NFX1	GRCh38.p7	9:33318590	TGCATAGGTCTGATC[A/G]GTACTCTATTTGGCC	4799
rs3942770	snp	A/C	0	0	intron-variant	NFX1	GRCh38.p7	9:33327989	TAAATCTTCTTTTTC[A/C]TCAGGCCCCACATCT	4799
rs4008680	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33363301	attattattattatt[A/T]ttagacagagtctca	4799
rs4878532	snp	C/T	0.313082	0.241911	intron-variant	NFX1	GRCh38.p7	9:33312688	CCAGGTGGGCCAACA[C/T]GGTGAAACCCCGTCT	4799
rs4878533	snp	C/T	0.0119091	0.0762411	intron-variant	NFX1	GRCh38.p7	9:33354594	ATAACAGAGAGGCCA[C/T]CATCCCACCTGTCCT	4799
rs4878534	snp	A/G	0.115383	0.210662	intron-variant	NFX1	GRCh38.p7	9:33354939	TTGCCCTTGAGCTCT[A/G]TGAAATTAATGGGAG	4799
rs4879682	snp	C/G	0.492823	0.0594727	intron-variant	NFX1	GRCh38.p7	9:33290690	AGCCACTCATATCGC[C/G]AGAGTAGCACATGCT	4799
rs4879683	snp	A/G	0.0279526	0.114869	intron-variant	NFX1	GRCh38.p7	9:33315974	TATTGTTCGAAACTC[A/G]GTGTTCTTTGAGTAC	4799
rs4879685	snp	A/G	0.493154	0.0581045	intron-variant	NFX1	GRCh38.p7	9:33335112	TGAAATTCACATAAC[A/G]TAATTAACCATTTTA	4799
rs4879686	snp	G/T	0.493837	0.055168	intron-variant	NFX1	GRCh38.p7	9:33343399	GAATAGCGGATACTT[G/T]GTTTAATAGAAGGTA	4799
rs4879688	snp	C/T	0.0970103	0.197722	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33366400	CCCTTTGTCCCTAAC[C/T]CTGTCCAGCTGCGAC	4799
rs5017299	snp	C/T			missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33342821	TGTGAAGAACCTTGT[C/T]ATCGTGGAAACTGCC	4799
rs5897541	in-del	-/T			intron-variant	NFX1	GRCh38.p7	9:33304853	TAGGACAATACCAAT[-/T]ACTTAATACCTTATT	4799
rs5897542	in-del	-/A	0.5	0	intron-variant	NFX1	GRCh38.p7	9:33317973	GTGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA	4799
rs7019355	snp	A/G	0.100231	0.200173	intron-variant	NFX1	GRCh38.p7	9:33298111	gaagacaggcagaaa[A/G]cacttagatatttaa	4799
rs7024137	snp	C/T	0.0984431	0.198823	intron-variant	NFX1	GRCh38.p7	9:33318169	GATCATTAGATCTTA[C/T]ACTCTCATGCCAATT	4799
rs7027207	snp	G/T	0.0152369	0.0859434	intron-variant	NFX1	GRCh38.p7	9:33354238	TCAATTAGACTTCAA[G/T]TAGAGGGCAGAGATT	4799
rs7033115	snp	A/G	0.0042729	0.0460238	intron-variant	NFX1	GRCh38.p7	9:33294400	TCTCTTTACTGGCAT[A/G]TCTATTTTTTATGTC	4799
rs7037491	snp	C/T	0.0126979	0.078662	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33353304	CTAAGCTCTGTGCTC[C/T]TCTGGTGTGAGGGTT	4799
rs7038216	snp	A/G	0.0479149	0.147179	intron-variant	NFX1	GRCh38.p7	9:33353719	ttgaaatggagtttc[A/G]ctcctgttgcccagg	4799
rs7039578	snp	C/T	0.0138799	0.0821421	intron-variant	NFX1	GRCh38.p7	9:33311621	gcagtggtgcgatct[C/T]ggctcactgcaacct	4799
rs7040601	snp	C/T	0.0980852	0.198549	intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33350217	GCTGAGGTAGGAGAA[C/T]CGCTTGAACCCAGGA	4799
rs7046204	snp	A/G	0.0444908	0.142359	upstream-variant-2KB	NFX1	GRCh38.p7	9:33290264	actgcactcaagcct[A/G]ggtaaggcagcaaga	4799
rs7048066	snp	G/T	0.0256215	0.110247	intron-variant	NFX1	GRCh38.p7	9:33334427	tgccattgcactcta[G/T]cctggtgacagagcg	4799
rs7848862	snp	A/G/T	0.0134861	0.0810011	intron-variant	NFX1	GRCh38.p7	9:33310597	CTAGCATGCCTCCCC[A/G/T]CATGTCAGCCTTCTT	4799
rs7866990	snp	C/T	0.0988009	0.199095	intron-variant	NFX1	GRCh38.p7	9:33301100	CTGCCCCTTTTTGGC[C/T]TCAGTCTGAATAGCC	4799
rs7867024	snp	C/G/T	0.0479149	0.147179	intron-variant	NFX1	GRCh38.p7	9:33311840	acaggcatgagctac[C/G/T]gcgctcggtcGGCAA	4799
rs7872396	snp	C/G	0.0475351	0.146656	intron-variant	NFX1	GRCh38.p7	9:33367981	gctcacgcctgtaat[C/G]ccagcactttgggag	4799
rs9695762	snp	A/G	0.0479149	0.147179	intron-variant	NFX1	GRCh38.p7	9:33315667	cagggcaggtggatc[A/G]cttgagcctaggagt	4799
rs9776553	snp	C/T	0.204496	0.245824	intron-variant	NFX1	GRCh38.p7	9:33342277	CCATCCTGGCTAACA[C/T]GGTGAAACCTCGTCT	4799
rs10046852	snp	A/G	0.110167	0.207236	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33365565	gtaagctgaggttga[A/G]tcactgtactccagc	4799
rs10119298	snp	C/G	0.124837	0.216412	intron-variant	NFX1	GRCh38.p7	9:33329371	agtctctcccgaggt[C/G]taccgataccatgtg	4799
rs10121445	snp	A/C	0.125182	0.216612	intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33349966	gagacacgattgtgc[A/C]actgccctccagcct	4799
rs10121477	snp	G/T	0.101658	0.201233	intron-variant	NFX1	GRCh38.p7	9:33333604	TACACTGTGTCCAAT[G/T]CTTCTGCCTAAACCT	4799
rs10123935	snp	C/T	0.0134861	0.0810011	intron-variant	NFX1	GRCh38.p7	9:33345425	gaggttgcagtgagc[C/T]gagactgtgccattg	4799
rs10125284	snp	A/G	0.101658	0.201233	intron-variant	NFX1	GRCh38.p7	9:33329163	acagagtccaaaaaa[A/G]taccaaaggtggaac	4799
rs10125308	snp	A/G	0.102726	0.202016	intron-variant	NFX1	GRCh38.p7	9:33329247	tgtgtgccagcatac[A/G]tggaatattgccaac	4799
rs10217130	snp	C/T	0.0390735	0.134201	intron-variant	NFX1	GRCh38.p7	9:33344045	TCAGAAAGGATTCTT[C/T]TGTTTTACCTGCTGC	4799
rs10511908	snp	A/G	0.124144	0.21601	intron-variant	NFX1	GRCh38.p7	9:33309915	TCTAGGTTATGTCAA[A/G]TATCTCAGAAGCCTG	4799
rs10552550	in-del	-/AC			intron-variant	NFX1	GRCh38.p7	9:33333138	GGCATGAGTCACCAC[-/AC]CGGCCTCGATTCCTG	4799
rs10664009	in-del	-/AAAA	0.5	0	upstream-variant-2KB	NFX1	GRCh38.p7	9:33290002	AAAAAAAAAAAAAAA[-/AAAA]GTCTGGAGCCAGGCG	4799
rs10813968	snp	A/G	0.492966	0.0588865	intron-variant	NFX1	GRCh38.p7	9:33291679	GAGGCCGAGGTGGAC[A/G]GATCACGAGGTCAGG	4799
rs10813969	snp	C/T	0.5	0	intron-variant	NFX1	GRCh38.p7	9:33335232	CTTTCTTTTTCTTTT[C/T]TTTTTTTTTTTTTTT	4799
rs10971463	snp	C/T	0.0930568	0.194599	intron-variant	NFX1	GRCh38.p7	9:33293059	GAGGTTACTCTATGA[C/T]CTTTATGATCATTCC	4799
rs10971464	snp	C/G	0	0	intron-variant	NFX1	GRCh38.p7	9:33295654	ATACAAATAAGAATT[C/G]TTTTTCTTTTCCAAA	4799
rs10971466	snp	C/G/T	0.123452	0.215605	intron-variant	NFX1	GRCh38.p7	9:33306974	TTTTTATTTATCTTT[C/G/T]CCAGGTAATCCAAGA	4799
rs10971467	snp	C/T	0	0	intron-variant	NFX1	GRCh38.p7	9:33315580	TCCCTGTGAAACATG[C/T]TCAGAGACCACACAT	4799
rs10971468	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33315720	ggcgaaaaccagtct[C/T]taacaacaacaaaaa	4799
rs10971469	snp	A/T	0.124491	0.216211	intron-variant	NFX1	GRCh38.p7	9:33315924	CAGATTGTTCACAAC[A/T]ATGCCAGTCTTTTTG	4799
rs10971470	snp	A/G	0.101658	0.201233	intron-variant	NFX1	GRCh38.p7	9:33330114	TGGATAGTTTTCATC[A/G]GACTTTATGTTATAA	4799
rs10971473	snp	C/T	0.100944	0.200705	intron-variant	NFX1	GRCh38.p7	9:33336876	GGAGGCCAAGGCAGG[C/T]GGATCACTTGAGGTC	4799
rs10971474	snp	C/G	0.101658	0.201233	intron-variant	NFX1	GRCh38.p7	9:33346206	AGGCCAGTCCCCACC[C/G]ATTGCCTCCTTTACA	4799
rs10971475	snp	C/T			intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33349906	cagctacttggaagg[C/T]taaggcaggaggatc	4799
rs10971476	snp	G/T	0.102726	0.202016	intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33350577	TCTGCTGCAAATCCT[G/T]TTGAGTCATAACAGG	4799
rs10971477	snp	C/T	0.0973687	0.197999	intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33351228	tttgggaggcctagg[C/T]gggtggatcgcttcc	4799
rs10971478	snp	A/G	0.00716266	0.059414	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33353012	cctcccaaagtgctg[A/G]gatcacaggcgtgag	4799
rs10971479	snp	A/G	0.102014	0.201495	intron-variant	NFX1	GRCh38.p7	9:33356214	GAGCTTTTAATTTCT[A/G]TTTTCCTGATGACTT	4799
rs10971480	snp	A/G	0.101658	0.201233	intron-variant	NFX1	GRCh38.p7	9:33356919	ATTGCTTGAACCTGC[A/G]AGGTTGAGGCTACAG	4799
rs10971481	snp	G/T	0	0	intron-variant	NFX1	GRCh38.p7	9:33359289	CAGTATATTGTTGAA[G/T]GGAGGGTGGTAATAA	4799
rs10971482	snp	A/G	0.111576	0.20818	intron-variant	NFX1	GRCh38.p7	9:33360127	TTAGGAGTCCTAGGT[A/G]TTCAGAAATGCTATA	4799
rs11364292	in-del	-/G	0.0325976	0.123435	intron-variant	NFX1	GRCh38.p7	9:33338692	GATTTAAAAGTCACT[-/G]GGACAGGCCCCTAAG	4799
rs11381680	in-del	-/A			intron-variant, downstream-variant-500B	NFX1, LOC105376018	GRCh38.p7	9:33348890	TACCAAAAAAAAAAA[-/A]GATATTGTTTTGTAA	4799
rs11394022	in-del	-/A/AA	0	0	intron-variant	NFX1	GRCh38.p7	9:33315903	CTCAAAAAAAAAAAA[-/A/AA]GTGGCCAGATTGTTC	4799
rs11452803	in-del	-/A			intron-variant	NFX1	GRCh38.p7	9:33315742	AACAAAAAAAAAAAA[-/A]TTAGCCAGACATGGT	4799
rs11452804	in-del	-/A/AA			intron-variant	NFX1	GRCh38.p7	9:33315898	CCCACCTCTGTCTCA[-/A/AA]AAAAAAAAAAAGTGG	4799
rs11787812	snp	C/G			intron-variant, utr-variant-3-prime	NFX1	GRCh38.p7	9:33348215	agccgggcctggtgg[C/G]gcatccctgtaatcc	4799
rs11788466	snp	C/T	0	0	intron-variant	NFX1	GRCh38.p7	9:33319965	CTTTTCTTTTCTTTT[C/T]TTTTTTTTTTTTTTG	4799
rs11789719	snp	A/C	0.100588	0.200439	intron-variant	NFX1	GRCh38.p7	9:33304803	AGAAAGGCAGCATGA[A/C]ACTGGAAGTAAGAGA	4799
rs11794927	snp	A/G	0.00947846	0.0681864	intron-variant	NFX1	GRCh38.p7	9:33294165	AGTACTTTATGGCCC[A/G]GGTGAGCATTTTTAC	4799
rs12001617	snp	A/G	0.0425829	0.139564	intron-variant	NFX1	GRCh38.p7	9:33293098	CTGTATGTTTCTATG[A/G]TACCCACTGCCCAAG	4799
rs12002437	snp	A/C	0.00358779	0.0422022	intron-variant	NFX1	GRCh38.p7	9:33310449	AATTCCGTATTGTAA[A/C]TTTTTTCTATTGGTC	4799
rs12005352	snp	A/G	0.0256215	0.110247	intron-variant	NFX1	GRCh38.p7	9:33333126	gttgggattacaggc[A/G]tgagtcaccacaccg	4799
rs12006301	snp	A/T	0.0263992	0.111815	intron-variant	NFX1	GRCh38.p7	9:33303351	GTCTGCGGGGCATGT[A/T]TTAGAAGTTACTAAT	4799
rs12115251	snp	C/T	0.101301	0.200969	intron-variant	NFX1	GRCh38.p7	9:33319650	aagtagctgggacta[C/T]aggcgcacaccacca	4799
rs12115762	snp	C/T	0.101301	0.200969	intron-variant	NFX1	GRCh38.p7	9:33321110	GTTTTATAAGAATTT[C/T]ACATATAATGACCAG	4799
rs12236764	snp	C/G	0.245061	0.249951	intron-variant	NFX1	GRCh38.p7	9:33359361	cccagcactttggga[C/G]actgaggcgggcgga	4799
rs12237401	snp	C/T	0.383053	0.211653	intron-variant	NFX1	GRCh38.p7	9:33367090	CTTTTCTCCTTCTGT[C/T]TCCTGTTCCTCTGTC	4799
rs12335968	snp	A/T	0.108402	0.206034	intron-variant	NFX1	GRCh38.p7	9:33304130	agctgggcatagtgt[A/T]gcatgtctgtaatcc	4799
rs12337652	snp	A/G	0.101658	0.201233	intron-variant	NFX1	GRCh38.p7	9:33337195	atgggttccatatcc[A/G]tggattcaaccaacc	4799
rs12338004	snp	A/G	0.110519	0.207473	intron-variant	NFX1	GRCh38.p7	9:33360649	cacgcatacacctgt[A/G]tgtatatatatgtat	4799
rs12338573	snp	A/C	0.101658	0.201233	intron-variant	NFX1	GRCh38.p7	9:33343103	TTCCTTCTCTGCTAC[A/C]TGCCTCATATGTGTT	4799
rs12339687	snp	G/T	0.100944	0.200705	intron-variant	NFX1	GRCh38.p7	9:33326481	cccagctactcagga[G/T]gctgaggtggaagga	4799
rs12340742	snp	A/G	0.10237	0.201756	intron-variant	NFX1	GRCh38.p7	9:33332887	gtctcgctctgtttc[A/G]caggccagagtgcag	4799
rs12340872	snp	A/T	0.0178098	0.0926698	intron-variant, utr-variant-3-prime, downstream-variant-500B	NFX1, LOC105376018	GRCh38.p7	9:33348363	tctcgaaaaaaaaaa[A/T]aaattttaaaaacta	4799
rs12341808	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33363559	agagtcctaggatta[C/T]tggtgtgagccaccg	4799
rs12342874	snp	A/G	0.109461	0.206758	intron-variant	NFX1	GRCh38.p7	9:33306338	AAGATGTGAACTTTG[A/G]CTGTGGATAAAGCCA	4799
rs12342956	snp	A/G	0.0142736	0.0832652	intron-variant	NFX1	GRCh38.p7	9:33306541	AGAAAAGCAGAGGCC[A/G]TGGACTGGGGATGGC	4799
rs12344357	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33300164	cccccgggttcaaga[A/G]attctcctgcctcat	4799
rs12344796	snp	A/G	0.102014	0.201495	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33353347	GTGAGGTATCTCTGC[A/G]GCCTCCTGAAGTCTT	4799
rs12344981	snp	A/C	0.141596	0.225274	intron-variant	NFX1	GRCh38.p7	9:33323760	ttcatctcaaaaaaa[A/C]aaacaaacaaaaaaa	4799
rs12346991	snp	G/T	0.0146672	0.084371	intron-variant	NFX1	GRCh38.p7	9:33358525	AAAAAAAATGCAAAT[G/T]ACAAGGACTTCATTT	4799
rs12348628	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33298559	aaggcagaaggattg[C/T]ttaagcccaggagtt	4799
rs12349432	snp	A/C	0.108048	0.20579	intron-variant	NFX1	GRCh38.p7	9:33304253	ggcgacagagtgaga[A/C]tccatctcaaaaaaa	4799
rs12351301	snp	A/G	0.111576	0.20818	intron-variant	NFX1	GRCh38.p7	9:33358511	GGTTGACATCCTCAA[A/G]AAAAAATGCAAATTA	4799
rs12351910	snp	A/G	0.146314	0.227484	intron-variant	NFX1	GRCh38.p7	9:33316497	TTTGTACAAATTTCT[A/G]TGGATCCCAGTCTCT	4799
rs12351915	snp	C/T	0.124144	0.21601	intron-variant	NFX1	GRCh38.p7	9:33316622	TAAATAGTTTATCTT[C/T]TTGAATTATAATCTT	4799
rs12352725	snp	A/T	0.101301	0.200969	intron-variant	NFX1	GRCh38.p7	9:33329881	ccaggctggtctcaa[A/T]ctcctgacctcaagt	4799
rs12353391	snp	A/G	0.122064	0.214785	intron-variant	NFX1	GRCh38.p7	9:33300413	TGTAATGTGCTTGCA[A/G]TGTTGTATTTAAGGT	4799
rs12353457	snp	C/T	0	0	intron-variant	NFX1	GRCh38.p7	9:33307794	TTTCTTTCtttcttt[C/T]ttttttttttttttt	4799
rs12377454	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33358288	caccactacacccgg[C/G]taattttttgtattt	4799
rs12551952	snp	A/G	0.00914312	0.0669923	intron-variant	NFX1	GRCh38.p7	9:33331948	CACTCACATGTAGTG[A/G]AAACCAAACTTTAGA	4799
rs12555104	snp	C/G	0.00914312	0.0669923	intron-variant	NFX1	GRCh38.p7	9:33305054	ACTTTGCCCCACACT[C/G]TTCTTCCAGGGGACc	4799
rs12555321	snp	A/C	0	0	intron-variant	NFX1	GRCh38.p7	9:33321421	TCTATAGAAAGCTCG[A/C]TTAGGTCTTTTGTAT	4799
rs12684157	snp	A/G	0	0	intron-variant	NFX1	GRCh38.p7	9:33333762	agtggccgtttggga[A/G]gtacccagcaatatc	4799
rs12684968	snp	C/T	0.226779	0.248919	intron-variant	NFX1	GRCh38.p7	9:33357411	ctgtcttaattactg[C/T]acctttataacaagt	4799
rs12685523	snp	C/T	0.207253	0.246318	intron-variant	NFX1	GRCh38.p7	9:33359099	cacttattTCTGATA[C/T]TGTAGATTATTTTGG	4799
rs12686729	snp	A/T	0.205417	0.245993	intron-variant	NFX1	GRCh38.p7	9:33368650	TGGCTAAAAGTTACT[A/T]CAAAGCCCAGAAGGA	4799
rs13286559	snp	A/G	0	0	intron-variant	NFX1	GRCh38.p7	9:33318429	TGTTCTCTTAATTTA[A/G]AGGTTGCTTCACTCT	4799
rs13286981	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33362693	aataagttcctgtgg[A/T]ttttttttttttttt	4799
rs13296323	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33297961	ttctatttaacaAAT[A/C]TCTTGGGGCCTTAAC	4799
rs13296327	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33297963	ctatttaacaAATCT[C/T]TTGGGGCCTTAACAT	4799
rs13301402	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33317975	tgagactctgtctca[A/C]aaaaaaaaaaaaaaa	4799
rs16919176	snp	A/G	0.031825	0.122064	intron-variant	NFX1	GRCh38.p7	9:33320361	AGAGTCATCATTTTT[A/G]TGAACTCCAGTTACT	4799
rs16919200	snp	C/T	0.097727	0.198275	intron-variant	NFX1	GRCh38.p7	9:33344366	AGCTTGGAATCACAG[C/T]GCCCTCCATTGGTTT	4799
rs16919219	snp	A/G	0.0130921	0.0798413	utr-variant-3-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33370513	ATCTTAAACCCAGCC[A/G]TCATACCTAAGTCTT	4799
rs17251129	snp	C/T	0.00517822	0.0506191	intron-variant	NFX1	GRCh38.p7	9:33316291	TGCAGAAAAGCTCTC[C/T]ATCCTGGTACTTACC	4799
rs28536141	snp	C/G/T	0.0170251	0.090679	intron-variant	NFX1	GRCh38.p7	9:33332852	CTTTGAACTTTTTTT[C/G/T]TTTTTCCTTTTGAGA	4799
rs33976056	in-del	-/T			intron-variant	NFX1	GRCh38.p7	9:33302378	TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTTAC	4799
rs34060097	in-del	-/A	0.140919	0.224948	intron-variant	NFX1	GRCh38.p7	9:33309361	GACTCCGTCTCAGAG[-/A]AAAAAAAAAAAAACT	4799
rs34095644	in-del	-/TT	0.49934	0.0181589	intron-variant	NFX1	GRCh38.p7	9:33325419	CTGTAATCCCAGCAC[-/TT]TGAGAGGCCGAGGCG	4799
rs34133819	in-del	-/A			intron-variant	NFX1	GRCh38.p7	9:33328315	AGGCATGAGCCACCA[-/A]CACTTGGCCTTTTTT	4799
rs34171064	in-del	-/C			intron-variant	NFX1	GRCh38.p7	9:33368552	AGCCCCAGTTGTCCC[-/C]AGTTGTTTGTCACTT	4799
rs34181227	in-del	-/A			intron-variant	NFX1	GRCh38.p7	9:33317676	TTAAAAAAAAAAAAA[-/A]TCTAGAGTCTTGATT	4799
rs34200962	in-del	-/C			intron-variant	NFX1	GRCh38.p7	9:33296610	ATGTTAGCACATGCC[-/C]TGTAGTCCCAGACAC	4799
rs34262554	in-del	-/A			intron-variant	NFX1	GRCh38.p7	9:33337282	TTTTCTCATCATTTT[-/A]CTAATAGCATTTACA	4799
rs34328727	in-del	-/C			intron-variant	NFX1	GRCh38.p7	9:33332226	GAATTTGGAGACCAG[-/C]ACCACAAAAATTGTT	4799
rs34358604	in-del	-/G			intron-variant	NFX1	GRCh38.p7	9:33361843	ATAGTGAAAAAAGGG[-/G]CCCGTTACAGCGGCT	4799
rs34444364	snp	A/C/T	0.000230636	0.0107364	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33319047	GTTTTCCGACTACTA[A/C/T]TTCCAAGTTCTAGCA	4799
rs34533184	in-del	-/A			intron-variant	NFX1	GRCh38.p7	9:33353946	CACCTGCCTTGGTTT[-/A]CCCAAAGTGCTGGGC	4799
rs34550711	in-del	-/C			intron-variant	NFX1	GRCh38.p7	9:33310439	GAATATACAAATTCC[-/C]GTATTGTAACTTTTT	4799
rs34632010	in-del	-/T			intron-variant	NFX1	GRCh38.p7	9:33294026	GTCCAAAGCCTGTTT[-/T]ACTTGATATTACACA	4799
rs34632825	in-del	-/A			intron-variant	NFX1	GRCh38.p7	9:33335747	TGATCTGCTTTCTAT[-/A]CTGTATGGATTTACT	4799
rs34707657	in-del	-/AAA	0.298905	0.24517	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352828	GAGTGGAGAAGAAAC[-/AAA]GAAGTCTGTAACTGT	4799
rs34707774	in-del	-/G			intron-variant	NFX1	GRCh38.p7	9:33359554	CAGTGAGCCGAGATG[-/G]CGCCACCACACTCTA	4799
rs34708441	in-del	-/C			intron-variant	NFX1	GRCh38.p7	9:33311446	TAACTAGTAGTTCCC[-/C]TGTGCTGCCCATGAC	4799
rs34712353	in-del	-/A			intron-variant	NFX1	GRCh38.p7	9:33359449	CTAAAAATACAAAAA[-/A]TTAGCCGGGCATGGT	4799
rs34750068	in-del	-/A			intron-variant	NFX1	GRCh38.p7	9:33362551	CACTCATATGTAGAA[-/A]TATTTAAAAAATAAT	4799
rs34822919	in-del	-/T			intron-variant	NFX1	GRCh38.p7	9:33311558	GACAAGGATTTTTTT[-/T]TTTTTTGAGACGGAG	4799
rs34826491	in-del	-/T			intron-variant	NFX1	GRCh38.p7	9:33300091	TTTTTTTTTTTTTTT[-/T]GAGACGGAGTCTCAC	4799
rs34878738	in-del	-/C			intron-variant	NFX1	GRCh38.p7	9:33330089	TGAGCCACTGTGCCC[-/C]AGCCTACCTTGGATA	4799
rs34924126	in-del	-/C			intron-variant	NFX1	GRCh38.p7	9:33315110	GGCGCCGGTAATCCC[-/C]AGGTACTTGGAGGCT	4799
rs34971771	snp	A/G	0.0271762	0.113356	intron-variant	NFX1	GRCh38.p7	9:33294039	TTTACTTGATATTAC[A/G]CAATGCTACTTTACT	4799
rs35058447	snp	C/T	0.0260105	0.111035	intron-variant	NFX1	GRCh38.p7	9:33308720	ATTAGTGCATCTATG[C/T]GGCTCGATATAGAGT	4799
rs35081523	in-del	-/T			intron-variant	NFX1	GRCh38.p7	9:33296511	GTGAGAGGATCACTT[-/T]GAACACAGGTGTTCA	4799
rs35087267	in-del	-/C			intron-variant	NFX1	GRCh38.p7	9:33361865	CAGCGGCTCATCCCC[-/C]ATAATCCCAGCATTT	4799
rs35141024	in-del	-/C			intron-variant	NFX1	GRCh38.p7	9:33368286	GGGTGTGGGGGTGAG[-/C]AATTGCCGGTGACGG	4799
rs35167820	in-del	-/G			intron-variant	NFX1	GRCh38.p7	9:33308894	GTGGTGGCGCTGGGG[-/G]AAATGTCAGTGGGGG	4799
rs35178105	in-del	-/C			frameshift-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33366704	TCCATGACTTGGCCC[-/C]AAGTTTATGGCCTGG	4799
rs35183496	in-del	-/T			intron-variant	NFX1	GRCh38.p7	9:33328206	TGCTTTTTTTTTTTT[-/T]GGTAGACACAGGGTT	4799
rs35185761	snp	A/G	0.226188	0.248863	intron-variant	NFX1	GRCh38.p7	9:33345714	TGTAAGTATTTTTTT[A/G]CAATATAAACTTTTA	4799
rs35268125	snp	A/C	0.0253123	0.109615	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33313757	AAGGCTGGCACTGAC[A/C]CCCATGGCACAGCTC	4799
rs35289045	in-del	-/C			intron-variant	NFX1	GRCh38.p7	9:33362578	AATACAGAAGCAGAG[-/C]AGTAGACCAGTGTTG	4799
rs35315823	snp	C/G	0.23846	0.249734	intron-variant	NFX1	GRCh38.p7	9:33326565	CCCTCAAAGAAATTT[C/G]TAAAATTACCCAGAC	4799
rs35323259	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33341490	CATAAACAAGGTAAC[A/C]CAGTACCAATAGCAA	4799
rs35343328	in-del	-/C			intron-variant, utr-variant-3-prime	NFX1	GRCh38.p7	9:33348222	CTGGTGGCGCATCCC[-/C]TGTAATCCCAGCTAC	4799
rs35391328	in-del	-/C			intron-variant	NFX1	GRCh38.p7	9:33316229	GAGTTGCCTGTGCCC[-/C]AGTTTGATTATCCAT	4799
rs35426919	in-del	-/T			intron-variant	NFX1	GRCh38.p7	9:33315015	TGTTTTTGATGTTTT[-/T]CAGTTTTTCTCTTCC	4799
rs35534651	in-del	-/A	0.5	0	intron-variant, utr-variant-3-prime, downstream-variant-500B	NFX1, LOC105376018	GRCh38.p7	9:33348506	GAAATAAGAAAAAAG[-/A]AAAAAAAAAAATCAC	4799
rs35554168	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33339982	TGCTTTCACAGGCTG[G/T]CATTGAGTGTCTGTG	4799
rs35555906	in-del	-/G			intron-variant	NFX1	GRCh38.p7	9:33340421	TGCATGCAGCAGGGG[-/G]ACCCTGGGGCCAGCC	4799
rs35570328	in-del	-/T			intron-variant	NFX1	GRCh38.p7	9:33326814	CTAACAAAGTAGTAT[-/T]GGGTTTATAACATAT	4799
rs35620555	in-del	-/T			intron-variant	NFX1	GRCh38.p7	9:33328736	TTTAAAATGGTGATT[-/T]ATGGGAGGGGAGGAA	4799
rs35723578	in-del	-/T			intron-variant	NFX1	GRCh38.p7	9:33302986	TTTTTTTTTTTTTTT[-/T]AATGAACCCCATATT	4799
rs35769483	in-del	-/C			utr-variant-3-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33370346	AGCCTCAGTTGTCCC[-/C]AGTTATTTGTCCTCC	4799
rs35782956	in-del	-/G			intron-variant	NFX1	GRCh38.p7	9:33367272	CTCTCAGAACCTGGG[-/G]AATAGGAAGAACTTG	4799
rs35844303	snp	A/G	0	0	intron-variant	NFX1	GRCh38.p7	9:33355263	TGTGCAGATCAGTGA[A/G]TCGTCACTAAATGAT	4799
rs35854489	in-del	-/CC	0.299411	0.245069	intron-variant	NFX1	GRCh38.p7	9:33342206	GGCTCATGCCTGTAA[-/CC]CCCCAGCACTTTGGG	4799
rs35866452	in-del	-/T	0.444267	0.157354	intron-variant	NFX1	GRCh38.p7	9:33355661	TTTTTTTTTTTTTTT[-/T]GAGATGGAGTTTTTC	4799
rs35938162	in-del	-/A			intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33350321	AAAAAAAAAAAAAAA[-/A]GGCAAAATAAAACGA	4799
rs35956049	snp	A/G	0.0941369	0.195465	upstream-variant-2KB	NFX1	GRCh38.p7	9:33289826	TTTCACGCAGGACAG[A/G]CTGCCCACCCTGTCC	4799
rs35979979	in-del	-/C			intron-variant	NFX1	GRCh38.p7	9:33297731	CCACCTGTGTTTCCC[-/C]TGCCACATGACTCTG	4799
rs35980358	in-del	-/T/TTT			intron-variant	NFX1	GRCh38.p7	9:33331695	TTTTTTTTTTTTTTT[-/T/TTT]CAGGATAATTTTTAC	4799
rs36049764	in-del	-/A			intron-variant	NFX1	GRCh38.p7	9:33368246	ATCTCAAAAAAAAAA[-/A]GAATAGTTACTCTGA	4799
rs36109934	in-del	-/A			intron-variant	NFX1	GRCh38.p7	9:33322217	AAAAAAAAAAAAAAA[-/A]GTCTCTAGAAATTGC	4799
rs41274031	snp	A/C	0.0233165	0.105426	intron-variant	NFX1	GRCh38.p7	9:33301457	GAGTAGTTATTCTCC[A/C]CTATTTGATACGTTT	4799
rs41274033	snp	A/G	0.0659589	0.169201	intron-variant	NFX1	GRCh38.p7	9:33303328	TGTACCTCAGTTCAG[A/G]AAAGGTGGTCTGCGG	4799
rs41274035	snp	A/G	0.0980852	0.198549	intron-variant	NFX1	GRCh38.p7	9:33310995	CAAATACAAAGACAT[A/G]TCATAGTAGATGTAT	4799
rs41274037	snp	A/C	0.0279168	0.1148	intron-variant	NFX1	GRCh38.p7	9:33344060	TTGTTTTACCTGCTG[A/C]TCCACCAGGTTTTGA	4799
rs55675308	snp	A/G			upstream-variant-2KB	NFX1	GRCh38.p7	9:33288521	GGCCTTGGCTGGTTG[A/G]CTGGGCCCAGCTCCT	4799
rs55695110	snp	A/G	0.108755	0.206276	intron-variant	NFX1	GRCh38.p7	9:33305575	ATTAGTTTGGTAGCA[A/G]TGAGTAGAGTATTTT	4799
rs55863878	snp	A/G	0.0314385	0.121371	intron-variant	NFX1	GRCh38.p7	9:33313327	GGCGTGGTGGCTCAA[A/G]CCTGTAATCCCAACA	4799
rs55984305	snp	A/G			upstream-variant-2KB	NFX1	GRCh38.p7	9:33289788	CAACTCCCCTTCCCT[A/G]GCCGCCCACTCACCC	4799
rs56293644	snp	C/T	0.00438332	0.0466095	intron-variant	NFX1	GRCh38.p7	9:33361979	AATACAAAAATTAGC[C/T]GGGCATGGTGGCACA	4799
rs56372045	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33335231	TCTTTCTTTTTCTTT[C/T]TTTTTTTTTTTTTTT	4799
rs57183366	in-del	-/C			intron-variant	NFX1	GRCh38.p7	9:33328762	GGAATCAAAATAACC[-/C]TCAGTAGATTAGGTA	4799
rs57459026	in-del	-/TT			intron-variant	NFX1	GRCh38.p7	9:33335246	TTTTTTTTTTTTTTT[-/TT]GAGACGGAGTTTTGC	4799
rs57525956	in-del	-/AATA			intron-variant	NFX1	GRCh38.p7	9:33341815	GTCTCTAAATAAATA[-/AATA]GATTTAAATGTAAAA	4799
rs57561473	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33362723	TTTTTTTTTTTTTGA[A/G]AAGGAGTTTTGCTCT	4799
rs57802012	in-del	-/TA			intron-variant	NFX1	GRCh38.p7	9:33339020	TTAAAAAGATTTTTT[-/TA]AAAATAAAATATTTA	4799
rs57828781	snp	A/G	0.00597247	0.0543191	intron-variant	NFX1	GRCh38.p7	9:33363140	TCAGGTGATGGATAT[A/G]CCTAATACACTGATT	4799
rs58280674	snp	C/T	0.00874735	0.0655527	intron-variant	NFX1	GRCh38.p7	9:33334980	CAACATTTTACCTCT[C/T]GTTTTCATCCATCCC	4799
rs58553141	in-del	-/T	0	0	intron-variant	NFX1	GRCh38.p7	9:33329645	TGGTTTTTATTTTTC[-/T]TTTTTTTTTTTTAAT	4799
rs58583054	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33336806	AAAAACTTAATTTTT[A/T]AAAGTTTTTCCAGGG	4799
rs58630959	snp	G/T	0.00597247	0.0543191	intron-variant	NFX1	GRCh38.p7	9:33335254	TTTTTTTTTGAGACG[G/T]AGTTTTGCTCTTGTT	4799
rs58683091	snp	G/T	0.101301	0.200969	intron-variant	NFX1	GRCh38.p7	9:33344857	GCGACAGACCAAGAC[G/T]CTGTCTCAAAAAAGA	4799
rs59461242	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33292815	GACATCTTTACTGAT[C/T]TTATTTCTGCCCCTC	4799
rs59623532	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33301964	GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAC	4799
rs59962836	in-del	-/GGGTGGGG	0	0	upstream-variant-2KB	NFX1	GRCh38.p7	9:33289495	GTCTGGGGGGTGGGG[-/GGGTGGGG]AGAAGTGTCGGGCAG	4799
rs60070379	in-del	-/AA			intron-variant	NFX1	GRCh38.p7	9:33309373	GAGAAAAAAAAAAAA[-/AA]CTTAATCCTCTGCAT	4799
rs60088224	snp	C/T	0.111928	0.208413	intron-variant	NFX1	GRCh38.p7	9:33364494	CTGGAGTCCCTGGCC[C/T]TTCAGTGGCTACTTC	4799
rs60137205	in-del	-/AA			intron-variant	NFX1	GRCh38.p7	9:33315241	AAAAAAAAAAAAAAA[-/AA]GGAATCTAGTTTTAT	4799
rs60147681	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33297816	CTTCAGATCTCTCTG[A/C]CTTCTGTTTGATTTT	4799
rs60654583	snp	A/G	0.0130921	0.0798413	intron-variant	NFX1	GRCh38.p7	9:33364597	TTCCTGATCTCTGCA[A/G]TTTTACTGCCAGCAT	4799
rs60776701	snp	A/G	0.192715	0.243348	intron-variant	NFX1	GRCh38.p7	9:33355476	TGTCTGGCTTCTTTC[A/G]TTATATTTTTGTGAC	4799
rs60850126	snp	A/G	0.0577344	0.159793	intron-variant	NFX1	GRCh38.p7	9:33297430	GAATCCTTAAGGCTG[A/G]TTAATAATTACCTCT	4799
rs60988084	in-del	-/A/ATT			intron-variant	NFX1	GRCh38.p7	9:33363300	ATTATTATTATTATT[-/A/ATT]TTTAGACAGAGTCTC	4799
rs61006461	snp	C/T	0.00953873	0.0683987	intron-variant	NFX1	GRCh38.p7	9:33346432	GTTCTTAACATTCTC[C/T]GAGAGGAGGAGGACA	4799
rs61084618	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33358883	GTTTTTTTTTTGGTA[A/G]AGATGGCATCTCGCT	4799
rs61227283	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33322321	AGTCTGTGGCATTGA[A/G]CCCTAGCTAGTTCCT	4799
rs61589629	in-del	-/T			intron-variant	NFX1	GRCh38.p7	9:33358680	TTTTTTTTTTTTTTT[-/T]GATACAGAGTCTCAC	4799
rs61662167	in-del	-/A			intron-variant	NFX1	GRCh38.p7	9:33321895	AAAAAAAAAAAAAAA[-/A]TCAACCATTTAAAGT	4799
rs62542700	snp	A/G	0.5	0	intron-variant	NFX1	GRCh38.p7	9:33307535	GATGAGGCTCAGAAA[A/G]GCCAAGCCTCTTGCC	4799
rs62542701	snp	C/T	0.0752113	0.178743	intron-variant	NFX1	GRCh38.p7	9:33310217	CACACTAATGTTTTA[C/T]AGCAAATTCTGTTAC	4799
rs62542722	snp	G/T	0.5	0	intron-variant	NFX1	GRCh38.p7	9:33316327	TTTTTTTTTTTTTTG[G/T]ATCTCGTTCTGTCAT	4799
rs62542723	snp	C/T	0.5	0	intron-variant	NFX1	GRCh38.p7	9:33316538	TTCTGTTTAGTTGAT[C/T]TTTCAAACCCAGTTT	4799
rs62542724	snp	G/T	0.207864	0.246424	intron-variant	NFX1	GRCh38.p7	9:33324544	AAGAAAGCAAGACCC[G/T]TTCTCAAAGGAAGAA	4799
rs62542725	snp	A/T	0.0980852	0.198549	intron-variant	NFX1	GRCh38.p7	9:33327509	CGCTGGGATTACAGG[A/T]GGGCGCCACCACGCC	4799
rs62542726	snp	A/G	0.5	0	intron-variant	NFX1	GRCh38.p7	9:33334939	AATGAATCCCCACGT[A/G]CCTATGACCTGTCAT	4799
rs62542727	snp	A/C	0.190833	0.242898	intron-variant	NFX1	GRCh38.p7	9:33334959	TGACCTGTCATCATC[A/C]GTTGTCAACATTTTA	4799
rs62542728	snp	C/T	0.0966517	0.197444	intron-variant	NFX1	GRCh38.p7	9:33336562	TGAAGTGATATATCA[C/T]TACCACATGATGTGA	4799
rs62542729	snp	C/T	0.0970103	0.197722	intron-variant	NFX1	GRCh38.p7	9:33341727	TTGATCCAAGGAATT[C/T]AAGGCCAGCCTTGGC	4799
rs62542731	snp	G/T	0.226188	0.248863	intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33349773	ATGAGTTGGGAGACA[G/T]GAGGAGAGTTAAGTA	4799
rs62542732	snp	C/T	0.0973687	0.197999	intron-variant	NFX1	GRCh38.p7	9:33353720	TGAAATGGAGTTTCG[C/T]TCCTGTTGCCCAGGC	4799
rs62542733	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33353737	CCTGTTGCCCAGGCT[A/G]GAGTGCAATGGTGCA	4799
rs62542735	snp	G/T	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33357545	CATTTATGTATTTAT[G/T]TATTGAGATAGGATC	4799
rs62542736	snp	G/T	0.190833	0.242898	intron-variant	NFX1	GRCh38.p7	9:33363565	CTAGGATTACTGGTG[G/T]GAGCCACCGCACCCA	4799
rs62542737	snp	A/G/T	1.64765e-05	0.00287019	synonymous-codon, missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33367521	TTTTATCAGGGGGAA[A/G/T]TCCGTTTGTCCTCCT	4799
rs67399088	snp	C/T	0.0263992	0.111815	intron-variant	NFX1	GRCh38.p7	9:33328930	AAGTTAGAGGAAACA[C/T]AGTCCATATGACCAC	4799
rs67519850	in-del	-/AAA			intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352829	AGTGGAGAAGAAACG[-/AAA]AAGTCTGTAACTGTT	4799
rs67591065	in-del	-/TTTAT			intron-variant	NFX1	GRCh38.p7	9:33354074	TTTTTCCCTTTCTTT[-/TTTAT]ATTTCAGAATAGCTG	4799
rs71485616	snp	C/T	0	0	intron-variant	NFX1	GRCh38.p7	9:33336404	TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT	4799
rs71485617	snp	C/T	0	0	intron-variant	NFX1	GRCh38.p7	9:33336412	GTAGAGACGGGGTTT[C/T]ACCATGTTGGCCAGG	4799
rs71506111	in-del	-/A	0.5	0	intron-variant	NFX1	GRCh38.p7	9:33308331	CTGTAGTCCCAGCTA[-/A]CTTGGGAGGCTGAGC	4799
rs72180208	in-del	-/TCT	0.445064	0.156365	intron-variant	NFX1	GRCh38.p7	9:33301774	TCTATTTTTAATTTA[-/TCT]TCTTCTCATTTTTGG	4799
rs72707406	snp	G/T	0.00597247	0.0543191	intron-variant	NFX1	GRCh38.p7	9:33322601	TGCAGCAGAATACTG[G/T]AGCCCTAATCGTCCT	4799
rs72707413	snp	G/T	0.00597247	0.0543191	intron-variant	NFX1	GRCh38.p7	9:33336681	CCACAGCTCACTGCA[G/T]CCTTGATCTCCTGGG	4799
rs72707417	snp	C/T	0.0162398	0.0886349	intron-variant	NFX1	GRCh38.p7	9:33346199	CATGCCCAGGCCAGT[C/T]CCCACCGATTGCCTC	4799
rs72723046	snp	C/T			upstream-variant-2KB	NFX1	GRCh38.p7	9:33289241	CTCCAGCCAGACCCC[C/T]GAAAGGAAGCAGGTG	4799
rs72723049	snp	C/T	0.0111196	0.0737302	intron-variant	NFX1	GRCh38.p7	9:33299450	AGTACTTTGGGAAAC[C/T]GAGTCAAGAGGATCA	4799
rs73476692	snp	C/G	0.0611083	0.163768	intron-variant	NFX1	GRCh38.p7	9:33298138	TTAATATGTCAGGTG[C/G]TGATAAGGACTAAAA	4799
rs73476696	snp	A/G	0.0115144	0.0749975	intron-variant	NFX1	GRCh38.p7	9:33308859	GATAATATTGGACCA[A/G]GGCCTTGTGATCAAG	4799
rs73476699	snp	C/T	0.0115144	0.0749975	intron-variant	NFX1	GRCh38.p7	9:33316517	TCCCAGTCTCTTCCT[C/T]CTTGTTTCTGTTTAG	4799
rs73478904	snp	C/T	0.0115144	0.0749975	intron-variant	NFX1	GRCh38.p7	9:33322542	AGTTAGGGCTCCCTT[C/T]CTCCACCAAGCTCCC	4799
rs73478912	snp	C/T	0.00953873	0.0683987	intron-variant	NFX1	GRCh38.p7	9:33332143	CTTGTTTGGTGATGA[C/T]TTCTCTTTCCTTTGC	4799
rs73478918	snp	C/T	0.0115144	0.0749975	intron-variant	NFX1	GRCh38.p7	9:33335636	CTCCCATGTTGGCCT[C/T]CCAAAGTGCTGGGGA	4799
rs73478923	snp	A/G	0.0372196	0.131242	intron-variant	NFX1	GRCh38.p7	9:33343365	CAAAAATTTTTTTAA[A/G]TAACTTTTCAAAAAA	4799
rs73478927	snp	A/C	0.0854556	0.188216	intron-variant	NFX1	GRCh38.p7	9:33346021	TATGATTCAGACTTA[A/C]AACTAGAAAACCAAC	4799
rs73478931	snp	C/G	0.0850919	0.187897	intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33350755	CAGCTAATCAGAAGA[C/G]TAAGGCAAGAGGCTC	4799
rs73478934	snp	A/G/T	0.0913286	0.193471	intron-variant	NFX1	GRCh38.p7	9:33356368	GTATTCTGAATATGA[A/G/T]TCCTTTGTTGGCTCT	4799
rs73478939	snp	C/T	0.0115144	0.0749975	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33364912	TGAGGATCCTTATCT[C/T]TCTCAAAACACAGCC	4799
rs73478940	snp	A/G	0.0901694	0.192235	intron-variant	NFX1	GRCh38.p7	9:33367170	GCTGGACTCTGGTTC[A/G]AGGCATCCCCTGTGA	4799
rs73478944	snp	A/C	0.00953873	0.0683987	utr-variant-3-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33370361	CAGTTATTTGTCCTC[A/C]TGAAAATGCCTGAAA	4799
rs73645268	snp	G/T	0.5	0	intron-variant	NFX1	GRCh38.p7	9:33291229	ATTTCCTCAGGGTGT[G/T]CCATAGATCAGTGTT	4799
rs73645269	snp	A/C	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33300809	TAGAGCCATCTCACC[A/C]CTCATGGGTTGTTGG	4799
rs73645270	snp	C/T	0.00358779	0.0422022	utr-variant-3-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33371083	GCAAGCCATGAGCCC[C/T]AGAGCAGTAGCAGGA	4799
rs74311950	in-del	-/GAGACTGGATAGAGTTCTACT			intron-variant	NFX1	GRCh38.p7	9:33321484	ACAGCTTCAGTATAA[-/GAGACTGGATAGAGTTCTACT]TTAAAGATGGTAGCA	4799
rs74348137	snp	G/T	0.00531737	0.0512875	intron-variant	NFX1	GRCh38.p7	9:33301244	GTTAATCTTTTTTGT[G/T]ATTTTGTTTTTTAAA	4799
rs74438074	snp	C/T	0.00557542	0.0525036	intron-variant	NFX1	GRCh38.p7	9:33339130	ATATAAAAAATATAA[C/T]GTATGCTATATATGA	4799
rs74451773	snp	C/T	0.00517822	0.0506191	intron-variant, downstream-variant-500B	NFX1, LOC105376018	GRCh38.p7	9:33349211	TGCTTTGGAAGTGAA[C/T]GAGACTAACCCTTGC	4799
rs74465802	snp	G/T	0.5	0	intron-variant	NFX1	GRCh38.p7	9:33335095	CCCACTTTTTTTTTA[G/T]TTGAAATTCACATAA	4799
rs74566916	snp	A/G	0.0126979	0.078662	intron-variant	NFX1	GRCh38.p7	9:33315977	TGTTCGAAACTCGGT[A/G]TTCTTTGAGTACATT	4799
rs74707263	snp	A/G	0.0232847	0.105357	intron-variant	NFX1	GRCh38.p7	9:33360293	TGAGACCTTGGGCAA[A/G]TCACATATTGTCTGT	4799
rs74708847	snp	A/G	0.0174175	0.0916809	intron-variant	NFX1	GRCh38.p7	9:33312216	GTGGCCTGAGATTAC[A/G]TGTAAGTGTTTTGAC	4799
rs74883784	snp	C/T	0.5	0	intron-variant	NFX1	GRCh38.p7	9:33346261	TGCTGCTGGGCAAGG[C/T]CCATAGTAAGAACTT	4799
rs74919894	snp	G/T	0	0	intron-variant	NFX1	GRCh38.p7	9:33353684	ATCTGATAGATTTGC[G/T]TTTTTTTTTTTTTTT	4799
rs75063899	snp	C/T	0.0134861	0.0810011	intron-variant	NFX1	GRCh38.p7	9:33363945	GATATAGTAGGCACT[C/T]GGGGTTACTGCAAGA	4799
rs75111863	snp	C/T	0	0	intron-variant	NFX1	GRCh38.p7	9:33313996	ATATAATTTTTTTTT[C/T]CTTTTTGAGATAAGT	4799
rs75173942	snp	A/G	0.0134861	0.0810011	intron-variant	NFX1	GRCh38.p7	9:33308492	GCAGTCAGCTTCTAA[A/G]TACCAAAAAATGCAC	4799
rs75179301	snp	C/G	0.124491	0.216211	intron-variant	NFX1	GRCh38.p7	9:33317460	AAAAGAAAAGAAATT[C/G]CACATGCACTTACTG	4799
rs75181385	snp	A/G	0.00789788	0.0623423	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33366646	AAAGAATAGTAAGAA[A/G]AGCCACAGCTTCCCT	4799
rs75231196	snp	A/C/G/T	0.0105887	0.0719985	missense, nc-transcript-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33351711	CCACAGTCAGCTCTG[A/C/G/T]GGGTGGTGCAGGGCT	4799
rs75252244	snp	A/G	0.0126979	0.078662	utr-variant-5-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33290482	CGGCGCGCAGATGCG[A/G]ATATTCTCGCGGCGC	4799
rs75411569	snp	G/T	0.5	0	intron-variant	NFX1	GRCh38.p7	9:33300092	TTTTTTTTTTTTTTT[G/T]AGACGGAGTCTCACT	4799
rs75421418	snp	A/C	0.5	0	intron-variant	NFX1	GRCh38.p7	9:33298784	ATAAGAACCTGTCTC[A/C]AAAAAAAAAATATTA	4799
rs75512284	snp	G/T	0.0984431	0.198823	intron-variant	NFX1	GRCh38.p7	9:33307562	TGCCCAGCATCACAG[G/T]GGCAGGGCGTGGATG	4799
rs75697802	snp	A/G	0.0103295	0.0711199	intron-variant	NFX1	GRCh38.p7	9:33354581	ACTCCTAGACCCCAT[A/G]ACAGAGAGGCCATCA	4799
rs75721607	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33317052	ACAAATATTTATTGT[A/G]TTTTCTGAATCTTTA	4799
rs75761465	snp	C/G	0.0174175	0.0916809	intron-variant	NFX1	GRCh38.p7	9:33292096	GACTCATTTCTGTAC[C/G]CTTCAGTGTTTGAAG	4799
rs75935212	snp	A/G	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33296843	AATTTGCATGCTTCT[A/G]TTACAGAACTTACAC	4799
rs75946862	snp	C/T	0.5	0	intron-variant	NFX1	GRCh38.p7	9:33320574	GTGGCTTCTGATTAC[C/T]TGAATATAGAAACCA	4799
rs76109044	snp	A/G	0.0256215	0.110247	intron-variant	NFX1	GRCh38.p7	9:33305655	CCTCTAAGGAGTGTG[A/G]TAGAAAAATATGGTG	4799
rs76169423	snp	A/G	0.0260105	0.111035	intron-variant	NFX1	GRCh38.p7	9:33326887	AATAGAGCTGTGTAA[A/G]GGTAAACCTTCTGTA	4799
rs76241407	snp	C/T	0.5	0	intron-variant	NFX1	GRCh38.p7	9:33341854	GGATGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC	4799
rs76248433	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33290842	CCGGCGCTGCGAGTC[C/G]ATGTGGGTGCCCTGC	4799
rs76394304	in-del	-/TT			intron-variant	NFX1	GRCh38.p7	9:33316324	GCCTTTTTTTTTTTT[-/TT]GGATCTCGTTCTGTC	4799
rs76482792	snp	C/G	0.0433465	0.140692	intron-variant	NFX1	GRCh38.p7	9:33358633	TAAGGCAAAAAAATT[C/G]TGTGAATGGCTTGAT	4799
rs76655712	snp	C/T	0.0209421	0.100162	intron-variant	NFX1	GRCh38.p7	9:33332076	AATGGTACAGATTGT[C/T]ATCTGTTTTCAATTC	4799
rs76670044	snp	C/T	0.0138799	0.0821421	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352889	TACATGTGTTTATCA[C/T]AGTATCCTTGCAACT	4799
rs76689382	snp	A/G	0.0221141	0.102801	intron-variant	NFX1	GRCh38.p7	9:33345889	GTATCTGTCAAGTCT[A/G]GTTGCTGGCTTTTCT	4799
rs76822493	snp	G/T	0.5	0	intron-variant	NFX1	GRCh38.p7	9:33353704	TTTTTTTTTTTTTTT[G/T]TGAAATGGAGTTTCG	4799
rs76864291	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33326408	ACAGAGCAAGCCTCT[G/T]TCTTTAAAAAAAAAA	4799
rs76870694	snp	G/T	0.021333	0.101051	intron-variant	NFX1	GRCh38.p7	9:33306213	CAACTTGGTGATTAA[G/T]TAGAAAGAGGTGTCA	4799
rs77096312	snp	C/T	0.0236746	0.106192	intron-variant	NFX1	GRCh38.p7	9:33322730	AGACCTTTCCCAGGG[C/T]GAGAGACAGTTCATA	4799
rs77128013	in-del	-/TT			intron-variant	NFX1	GRCh38.p7	9:33311867	GCAAGGATTTTTTTT[-/TT]AACCTCTCTAAGTGG	4799
rs77172042	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33292824	ACTGATCTTATTTCT[G/T]CCCCTCTTTCCAGTC	4799
rs77249146	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33292347	TAAACAGAAGCCCAG[C/T]GCAGAGGATACTTTT	4799
rs77309774	in-del	-/AAAACAAAAAC			intron-variant	NFX1	GRCh38.p7	9:33337752	AAAACAAAACAAAAC[-/AAAACAAAAAC]TGATGGCCGGGCATG	4799
rs77354389	snp	G/T	0.5	0	intron-variant	NFX1	GRCh38.p7	9:33300088	TTTTTTTTTTTTTTT[G/T]TTTGAGACGGAGTCT	4799
rs77366692	snp	A/G	0.0486741	0.148216	intron-variant	NFX1	GRCh38.p7	9:33329007	CCTAAGACCACCTGC[A/G]AGGCTTGATAATTTG	4799
rs77431195	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33317051	TACAAATATTTATTG[C/T]GTTTTCTGAATCTTT	4799
rs77469097	snp	C/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33345535	TCTATTATATGTCAC[C/G]TCCAAAGAATTATAC	4799
rs77573079	snp	G/T			intron-variant	NFX1	GRCh38.p7	9:33317053	CAAATATTTATTGTG[G/T]TTTCTGAATCTTTAT	4799
rs77577339	snp	A/C/T	0.0408579	0.137964	intron-variant	NFX1	GRCh38.p7	9:33304240	GCACTCCAGCCTGGG[A/C/T]GACAGAGTGAGACTC	4799
rs77598372	in-del	-/AA			intron-variant	NFX1	GRCh38.p7	9:33359612	TCACCAAAAAAAAAA[-/AA]TAGATGTTCCTGACT	4799
rs77659068	snp	A/G	0.0479149	0.147179	intron-variant	NFX1	GRCh38.p7	9:33305184	AAGAGTTAAAACACA[A/G]TTAGCCTGATACTCT	4799
rs77746257	snp	G/T	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33311570	GGATTTTTTTTTTTT[G/T]GAGACGGAGTCTCGG	4799
rs77804000	snp	A/C	0.0197687	0.0974348	intron-variant	NFX1	GRCh38.p7	9:33360596	ATTTAAAGAAAAGTC[A/C]ATCTAAAGTTATATC	4799
rs77904344	snp	A/C			intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33364916	GATCCTTATCTTTCT[A/C]AAAACACAGCCATTA	4799
rs78078622	snp	C/G	0.0126979	0.078662	intron-variant	NFX1	GRCh38.p7	9:33327244	TTCCTGGGCTGATCC[C/G]GAACTCCTAGGCTCA	4799
rs78085919	snp	A/G	0.0966517	0.197444	intron-variant	NFX1	GRCh38.p7	9:33335332	ACCTCCTGGGCTCAA[A/G]CAATTCTCCTGTCTT	4799
rs78096700	snp	G/T	0.5	0	intron-variant	NFX1	GRCh38.p7	9:33300087	TTTTTTTTTTTTTTT[G/T]TTTTGAGACGGAGTC	4799
rs78099178	snp	A/C	0	0	intron-variant	NFX1	GRCh38.p7	9:33317422	AGGCCCTGTCTCCAA[A/C]AAAAAAAAAAAAAGA	4799
rs78192843	snp	A/C			upstream-variant-2KB	NFX1	GRCh38.p7	9:33289273	TCCCCCACTTCCAGG[A/C]CTTAGTTGGGGCGGG	4799
rs78281734	snp	A/G	0.5	0	intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33349676	AGGCCATTTTTCAAG[A/G]AAAAAAAAAAGAATT	4799
rs78299931	snp	A/G	0.0150606	0.0854603	intron-variant	NFX1	GRCh38.p7	9:33355575	ACTATTCATTTACCC[A/G]TTATACTGTTAATGG	4799
rs78300540	snp	A/G	0.0980852	0.198549	intron-variant	NFX1	GRCh38.p7	9:33326286	GGTGTGGTGGCATAT[A/G]CCTGTGATCCCAGCT	4799
rs78362561	snp	C/T	0.5	0	intron-variant	NFX1	GRCh38.p7	9:33328195	TCTTGTTTTTGTGCT[C/T]TTTTTTTTTTTGGTA	4799
rs78385710	in-del	-/T			intron-variant	NFX1	GRCh38.p7	9:33301779	TTTTAATTTATCTTC[-/T]TCTCATTTTTGGCCA	4799
rs78449514	snp	A/T	0.5	0	upstream-variant-2KB	NFX1	GRCh38.p7	9:33290296	CCTATATCAAAAAAT[A/T]AAAAAAGGAAAACCA	4799
rs78451763	snp	A/C/T	0.000132031	0.00812391	intron-variant	NFX1	GRCh38.p7	9:33354077	TTCCCTTTCTTTTTT[A/C/T]TATTTCAGAATAGCT	4799
rs78514588	snp	C/G	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33315393	GATACAACTCTAATC[C/G]TCCCAGTTTTTTCTT	4799
rs78592152	snp	G/T	0.0252325	0.109451	intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33350568	TTTTTGGCTTCTGCT[G/T]CAAATCCTTTTGAGT	4799
rs78631374	snp	A/T	0.5	0	intron-variant	NFX1	GRCh38.p7	9:33335093	AGCCCACTTTTTTTT[A/T]AGTTGAAATTCACAT	4799
rs78695051	snp	C/T	0.123452	0.215605	intron-variant	NFX1	GRCh38.p7	9:33314448	TTGAGAGGGTGAGGC[C/T]GGTGGATCACTCGAG	4799
rs78745052	snp	A/G	0.0441095	0.141807	intron-variant, utr-variant-3-prime, downstream-variant-500B	NFX1, LOC105376018	GRCh38.p7	9:33348665	GACAGGGTTGCCACA[A/G]AGTTTCAATTTGTAA	4799
rs78778092	in-del	-/TT			intron-variant	NFX1	GRCh38.p7	9:33357720	CTTTTTTTTTTTTTT[-/TT]CTTTTGTAAAGACAG	4799
rs78828456	snp	A/T	0.00398564	0.0444627	intron-variant	NFX1	GRCh38.p7	9:33347476	ACTTTAAAATACCAA[A/T]TTTTTTTTTAATAAC	4799
rs78936795	snp	C/T	0.0984431	0.198823	intron-variant	NFX1	GRCh38.p7	9:33307046	ATTATATTTATCTTT[C/T]TATTTTAAGATATGG	4799
rs78984357	snp	C/T	0.00835141	0.0640778	intron-variant	NFX1	GRCh38.p7	9:33291154	TTGTTCACTCACTCC[C/T]CCTCCTGGAGTTGCC	4799
rs79012509	snp	G/T	0.5	0	intron-variant	NFX1	GRCh38.p7	9:33316325	CCTTTTTTTTTTTTT[G/T]GGATCTCGTTCTGTC	4799
rs79044176	snp	A/G	0.5	0	intron-variant	NFX1	GRCh38.p7	9:33335094	GCCCACTTTTTTTTT[A/G]GTTGAAATTCACATA	4799
rs79262904	snp	A/G	0.0916144	0.193427	intron-variant	NFX1	GRCh38.p7	9:33362399	TGGATAAAGAAAATG[A/G]GGTATATATACAGAA	4799
rs79303538	snp	A/C	0.5	0	intron-variant	NFX1	GRCh38.p7	9:33346445	TCCGAGAGGAGGAGG[A/C]CAGTAGTTCAATACA	4799
rs79441880	snp	C/T	0.0256215	0.110247	intron-variant	NFX1	GRCh38.p7	9:33343177	ATTAGCAGCAGTTTG[C/T]AAACTTTTTGGTTGT	4799
rs79470721	snp	G/T	0.0479149	0.147179	intron-variant	NFX1	GRCh38.p7	9:33330313	GGCAGCATCTGACTT[G/T]CGAATAATTCTGAGG	4799
rs79637107	snp	A/G	0.00557542	0.0525036	intron-variant	NFX1	GRCh38.p7	9:33293479	CTGCAACTCTTTGAT[A/G]TAGAGGTTGTTACTA	4799
rs79679085	snp	A/T	0.0170251	0.090679	intron-variant	NFX1	GRCh38.p7	9:33347485	TACCAAATTTTTTTT[A/T]AATAACCTCCTTATT	4799
rs79701879	snp	A/G	0.0456336	0.143994	intron-variant	NFX1	GRCh38.p7	9:33297637	TTGTTGGTAGGATTC[A/G]GTTCCTTACAGATGT	4799
rs79744127	snp	C/T	0.00199481	0.0315187	intron-variant	NFX1	GRCh38.p7	9:33362005	GCACACTTGTAGTGC[C/T]AGCTACTGGAGAGGT	4799
rs79819765	snp	A/G	0.0150606	0.0854603	intron-variant	NFX1	GRCh38.p7	9:33332045	GAAGTGTGTAGAGCC[A/G]TTTGTCCCTGCATTA	4799
rs79845235	snp	C/T	0.0103295	0.0711199	intron-variant	NFX1	GRCh38.p7	9:33360991	GCCATGAGATTCAGA[C/T]ACTGATGGCTAGGGC	4799
rs79989223	snp	A/T	0.5	0	intron-variant	NFX1	GRCh38.p7	9:33300065	TACCTATGTTATAGC[A/T]TTTTTTTTTTTTTTT	4799
rs80052565	snp	C/T	0	0	intron-variant	NFX1	GRCh38.p7	9:33342089	CCACCACACTCCAGC[C/T]TGGGCAACAGAGTGA	4799
rs80217601	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33317433	CCAAAAAAAAAAAAA[A/T]AAGAAAGAAAGAAAA	4799
rs80316528	snp	C/T	0.0260105	0.111035	intron-variant	NFX1	GRCh38.p7	9:33318538	GGTAAAGCTCTTAGG[C/T]GGGTCTTAGAGCTGC	4799
rs80356366	in-del	-/T			intron-variant	NFX1	GRCh38.p7	9:33314975	ATGAATAGAAAAAAA[-/T]TTTTTTAATTGTGAA	4799
rs111261562	snp	C/G	0.5	0	intron-variant	NFX1	GRCh38.p7	9:33310842	ATGTCATCTTTGACT[C/G]TCAGACCCAAATATA	4799
rs111273722	snp	A/T	0.00438332	0.0466095	intron-variant	NFX1	GRCh38.p7	9:33369814	TGTTTAAGATTCACA[A/T]ATGGTAAATCAGCTG	4799
rs111306917	in-del	-/TTTTT	0	0	intron-variant	NFX1	GRCh38.p7	9:33353684	ATCTGATAGATTTGC[-/TTTTT]TTTTTTTTTTTTTTT	4799
rs111311257	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33319970	CTTTTCTTTTCTTTT[C/T]TTTTTTTTTGAGACA	4799
rs111324389	snp	A/G	0.5	0	intron-variant	NFX1	GRCh38.p7	9:33326486	CTACTCAGGAGGCTG[A/G]GGTGGAAGGATCACT	4799
rs111528666	snp	C/T	0.0115144	0.0749975	intron-variant	NFX1	GRCh38.p7	9:33358947	CAAGCAATCCTCCTG[C/T]CTCAGCCTTCCAAAG	4799
rs111584716	snp	C/T	0.5	0	intron-variant	NFX1	GRCh38.p7	9:33346956	TTAAAAGTTTCATGC[C/T]GTATGCCACTTATAT	4799
rs111613978	snp	A/G	0.5	0	intron-variant	NFX1	GRCh38.p7	9:33338337	TCCAGCCTGGGCGAC[A/G]GAGAAAGACTCCATC	4799
rs111733942	snp	A/G	0.0115144	0.0749975	intron-variant	NFX1	GRCh38.p7	9:33320154	TATTTTTGTAGAGAC[A/G]GGGTTTCACCATGTT	4799
rs111822743	snp	A/C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33337921	GGGCGTGGTGGCGCA[A/C/T]ACCTGTAATCCCAGC	4799
rs111859910	snp	A/G	0	0	intron-variant	NFX1	GRCh38.p7	9:33343800	ATTAATATAATCTCC[A/G]GTCTAGAAATATGTT	4799
rs111959382	in-del	-/TCTT	0.5	0	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33353174	CCGCTTCCTCCTTCC[-/TCTT]TCTTTTTTTCTCTCT	4799
rs111983358	snp	C/T	0.0581099	0.160244	intron-variant	NFX1	GRCh38.p7	9:33312668	TTGAGGTTAAGAGTT[C/T]GAGACCAGGTGGGCC	4799
rs112070228	snp	C/T			synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33366661	AAGCCACAGCTTCCC[C/T]CCCATGAACAGAGAC	4799
rs112101294	snp	A/C	0	0	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352828	GGAGTGGAGAAGAAA[A/C]GAAGTCTGTAACTGT	4799
rs112109866	snp	C/T	0.5	0	intron-variant	NFX1	GRCh38.p7	9:33313936	GATACGATGCTTAGA[C/T]GGTTTTTATTATTTT	4799
rs112143826	snp	A/G			intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352829	GAGTGGAGAAGAAAC[A/G]AAGTCTGTAACTGTT	4799
rs112160926	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33342121	ACCCTGTCTCTGTCT[C/G]TCTCTCTCACACACA	4799
rs112198129	snp	C/T	0.5	0	utr-variant-3-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33370233	CAAAGAGGCTCTTTA[C/T]ACCATCACTGTGATT	4799
rs112200158	in-del	-/A	0	0	intron-variant	NFX1	GRCh38.p7	9:33317663	TGAGATCCTGTCTTT[-/A]AAAAAAAAAAAAATC	4799
rs112206321	snp	G/T	0.0322114	0.122752	intron-variant	NFX1	GRCh38.p7	9:33359355	TGTAATCCCAGCACT[G/T]TGGGAGACTGAGGCG	4799
rs112316279	snp	C/G			upstream-variant-2KB	NFX1	GRCh38.p7	9:33289577	GGTTGTGCCTTACCT[C/G]AGGAGCCACCCGTTC	4799
rs112322350	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33315524	ATATTCTTTCCCCAG[C/T]GTTTCCTTTCAGGCC	4799
rs112399410	snp	A/G	0.5	0	intron-variant	NFX1	GRCh38.p7	9:33338390	AAAAACTGCATTTAC[A/G]TTATTACAATTGTAT	4799
rs112409354	snp	C/T	0.00517822	0.0506191	intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33350099	ACCTGAGGTCAGCAG[C/T]TGGAGACCAGCCTGG	4799
rs112441794	snp	A/T	0.5	0	intron-variant	NFX1	GRCh38.p7	9:33342699	TTATTTATGGAAAAT[A/T]TAAAATGAAGACCAT	4799
rs112443114	snp	A/G	0.5	0	intron-variant	NFX1	GRCh38.p7	9:33324944	AAAAAAAAAAAAAAA[A/G]AAAGAGATTATATAA	4799
rs112522551	snp	A/G	0.0314385	0.121371	intron-variant	NFX1	GRCh38.p7	9:33362797	CAAGCTCTGCCTCCC[A/G]GGTTCAAGCGATTCT	4799
rs112527259	snp	A/G	0.00478085	0.0486577	intron-variant	NFX1	GRCh38.p7	9:33340602	TGATTTTCTTCTCAG[A/G]AAATAGGATTTTCTT	4799
rs112614986	snp	C/T	0.5	0	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33366480	CCAAACCCCTCCAGG[C/T]TTGCTTGGCAGTTAG	4799
rs112660568	snp	C/T	0.00676609	0.0577691	intron-variant	NFX1	GRCh38.p7	9:33319344	GATTCAGGTATTTTA[C/T]TGTTAACTCTGGACA	4799
rs112720396	snp	A/G	4.962e-05	0.00498072	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33351694	GGATGAGCCCTGCAA[A/G]CAGCCCTGCACCACC	4799
rs112772680	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33315361	TCACTGTATTTTTAG[G/T]TAGGCTGTTTAGTCA	4799
rs112779908	snp	C/G	0.5	0	intron-variant	NFX1	GRCh38.p7	9:33312842	CTCCACTGCACTCCA[C/G]CCTGGGCAACAGAGC	4799
rs112809951	snp	A/T	0.5	0	intron-variant	NFX1	GRCh38.p7	9:33329711	TCACCCAGGATGGAG[A/T]GCAGAGGCGCAGTCT	4799
rs112854220	in-del	-/A/AA/AAA	0.661118	0.0413823	intron-variant	NFX1	GRCh38.p7	9:33315891	ACCCACCTCTGTCTC[-/A/AA/AAA]AAAAAAAAAAAAGTG	4799
rs112857164	snp	A/G	0.0349115	0.127424	intron-variant	NFX1	GRCh38.p7	9:33344739	GGCATGGTGGTGCAC[A/G]CCTGTAGTCCCAGCT	4799
rs112941102	snp	A/G	0.00350917	0.0417405	intron-variant, missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33347684	CACTACTGGGCGTCT[A/G]CCCAGAAGAAAAGAA	4799
rs113004437	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33333213	CTTTTTGGAAAAGTG[A/G]TGGAAGATAAGGATA	4799
rs113081500	snp	G/T	0.5	0	intron-variant	NFX1	GRCh38.p7	9:33295921	AGAGAGCAATCTTTA[G/T]AAAACACATATTTTA	4799
rs113189575	snp	C/T	0.0252325	0.109451	intron-variant	NFX1	GRCh38.p7	9:33298610	TAATGAGACCCCATC[C/T]CTGCAAAAGGCAAAA	4799
rs113205823	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33331034	AGCCAGGCACGGTGG[A/T]GGGCGCCTGTAGTCC	4799
rs113300226	snp	C/T	0.5	0	intron-variant	NFX1	GRCh38.p7	9:33355050	CCAAGAATTGAATTG[C/T]CTTAAGGATAAACCA	4799
rs113313466	snp	C/T	0.5	0	intron-variant	NFX1	GRCh38.p7	9:33300956	CAAGATCCTGTATTG[C/T]CCAGTGGATCCTCAG	4799
rs113334795	snp	G/T	0.5	0	intron-variant	NFX1	GRCh38.p7	9:33313113	TCCAGGCAGAGCTAG[G/T]ACCAGAACCCAGATC	4799
rs113341276	snp	C/T	0.0573587	0.15934	intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33351260	CTCAAGAGTTCGAGA[C/T]CAGCCTGGGCAACAT	4799
rs113433967	snp	A/C/G	1.64738e-05	0.00286995	intron-variant	NFX1	GRCh38.p7	9:33318843	CAAGTAAGGTTTTAC[A/C/G]TTTTCTTCAGTTGAA	4799
rs113516912	snp	A/C/T	0.0479149	0.147179	intron-variant	NFX1	GRCh38.p7	9:33340042	AGTGGATCTCCCATT[A/C/T]TGGGGTCTGGAGGAC	4799
rs113527156	in-del	-/T	0.5	0	intron-variant	NFX1	GRCh38.p7	9:33347246	TCCATTGCTTAAAAA[-/T]TTTTTTCTTAAGATA	4799
rs113545762	snp	C/T	0.00953873	0.0683987	intron-variant	NFX1	GRCh38.p7	9:33345345	AGCCTGGCGTGGTGG[C/T]GGACGCCTGTAATCC	4799
rs113573951	snp	A/G	0.0023933	0.0345097	intron-variant	NFX1	GRCh38.p7	9:33368021	GGTGGATCACTTAAG[A/G]TCAGGAGTTCGAGAC	4799
rs113592819	snp	A/C	0.00676609	0.0577691	intron-variant	NFX1	GRCh38.p7	9:33312926	CTCAGCAAAATCAGG[A/C]TGTTTATTAGAACAA	4799
rs113616089	snp	A/C/G	0	0	splice-acceptor-variant	NFX1	GRCh38.p7	9:33318909	TGTGTTTTCTTAACA[A/C/G]GGACTTGAAATGCGG	4799
rs113745700	in-del	-/A	0.5	0	intron-variant	NFX1	GRCh38.p7	9:33298784	ATAAGAACCTGTCTC[-/A]AAAAAAAAAATATTA	4799
rs113797063	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33303366	TTTAGAAGTTACTAA[C/T]GAGACTTCAAAGCTC	4799
rs113811633	snp	A/G	0.444444	0.157135	intron-variant	NFX1	GRCh38.p7	9:33360657	CACCTGTGTGTATAT[A/G]TATGTATGTGTGTAT	4799
rs113830791	snp	C/T	0.00914312	0.0669923	intron-variant	NFX1	GRCh38.p7	9:33323942	TAAAAGTAGGATAAC[C/T]GAAATGCAAAATTCA	4799
rs113845564	snp	C/T	0.5	0	intron-variant	NFX1	GRCh38.p7	9:33307798	TTTCTTTCTTTCTTT[C/T]TTTTTTTTTTTTTTT	4799
rs114019569	snp	C/T	0.0256215	0.110247	intron-variant	NFX1	GRCh38.p7	9:33308269	CAACAAAATGAGACC[C/T]CGTCTCTACAAAAAA	4799
rs114231070	snp	C/T	0.00274745	0.0369618	intron-variant	NFX1	GRCh38.p7	9:33318877	AAGCTGCACTTTATG[C/T]AACAATTATGTAATA	4799
rs114289781	snp	A/G	0.0479149	0.147179	intron-variant, utr-variant-3-prime	NFX1	GRCh38.p7	9:33348031	GGACTCTGGGGAAAG[A/G]ACGGGAGGCGGGTGA	4799
rs114377255	snp	C/T	0.00211963	0.0324857	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33369926	CTGGGAGCAGTAATT[C/T]ACAGAAAATAACCAA	4799
rs114516137	snp	C/T	0.0248432	0.108648	intron-variant	NFX1	GRCh38.p7	9:33305912	CACAGCTGAGAGGAG[C/T]AGTTAAGACCCTAGC	4799
rs114596797	snp	A/G	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33361835	GAAACGTTATAGTGA[A/G]AAAAGGGGCCCGTTA	4799
rs114609874	snp	C/G	0.0126979	0.078662	intron-variant	NFX1	GRCh38.p7	9:33291933	AAAACACACTGCATT[C/G]GTGTACCCTAGTCTT	4799
rs114634847	snp	G/T	0.0103295	0.0711199	intron-variant	NFX1	GRCh38.p7	9:33359820	AGAATTTAGGTGAAG[G/T]TTATATAGAAGTTTA	4799
rs114674352	snp	A/G	0.0252325	0.109451	intron-variant	NFX1	GRCh38.p7	9:33293505	TACTATCTTCATTAC[A/G]TGTAAGGAAAATGGG	4799
rs114721168	snp	A/G	0.00287387	0.0377978	intron-variant	NFX1	GRCh38.p7	9:33290613	GTATTGTCCCGGCCC[A/G]AGCGGGACTGGGCCC	4799
rs114721508	snp	A/G	0.0174175	0.0916809	intron-variant	NFX1	GRCh38.p7	9:33337655	GCTCATTTGAGTGCA[A/G]GAATTCGAGGTTACA	4799
rs114796802	snp	A/C	0.0429648	0.14013	intron-variant	NFX1	GRCh38.p7	9:33312442	TGATCATTTATGTAC[A/C]TAACAGTGACTTTTA	4799
rs114843698	snp	C/T	0.0217236	0.101931	utr-variant-5-prime, upstream-variant-2KB	NFX1	GRCh38.p7	9:33290429	GTCACGAACGCGCCA[C/T]ACAGATTCGGGCTGC	4799
rs114847998	snp	C/T	0.0225045	0.103662	intron-variant	NFX1	GRCh38.p7	9:33319907	ATCTAGCTGAGGATA[C/T]GAGGATAGCACCTAT	4799
rs114863466	snp	A/G	0.0479149	0.147179	intron-variant	NFX1	GRCh38.p7	9:33333650	AATGGAATTACCATG[A/G]TGGGTAAAGGTACAC	4799
rs114876875	snp	A/C	0.0103295	0.0711199	intron-variant	NFX1	GRCh38.p7	9:33300464	ATTTAGACCTGAAAG[A/C]AAATAACAATAATAT	4799
rs115063688	snp	A/G	0.0130921	0.0798413	intron-variant	NFX1	GRCh38.p7	9:33303965	TGCCTCACTGAAACC[A/G]TATTCAGAAATTACC	4799
rs115134921	snp	A/G	0.0248432	0.108648	intron-variant	NFX1	GRCh38.p7	9:33310684	GTCTGTACTTCTTAC[A/G]GACCAGGTAGATTTG	4799
rs115182494	snp	A/G	0.0345262	0.126772	intron-variant	NFX1	GRCh38.p7	9:33308170	CCATAAGCCAGACAC[A/G]GTGGCTCATGCCTAT	4799
rs115327076	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33323116	TCGGGAATCAAGACA[A/G]AGAGAGCCCTGCTTG	4799
rs115328105	snp	C/T	0.0130921	0.0798413	intron-variant	NFX1	GRCh38.p7	9:33333347	GGGTGTTTACTGCCA[C/T]ACCTGATAGGATATC	4799
rs115399783	snp	A/T	0.00478085	0.0486577	intron-variant	NFX1	GRCh38.p7	9:33290925	CGTCGGCCAGGTCAC[A/T]GCCAGTGACGGTGGC	4799
rs115521821	snp	C/T	0.0193772	0.0965046	intron-variant	NFX1	GRCh38.p7	9:33306352	GACTGTGGATAAAGC[C/T]AGTTTGAGGTGACTG	4799
rs115523120	snp	A/G	0.0134861	0.0810011	intron-variant	NFX1	GRCh38.p7	9:33307989	TTGTATGTTTTGGTA[A/G]AAATGGGGTTTTGCC	4799
rs115594798	snp	A/G	0.0248432	0.108648	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352965	ATTGAGAGGGGTCTC[A/G]CCCTGTTTCCCAGGC	4799
rs115725685	snp	C/T	0.0256215	0.110247	intron-variant	NFX1	GRCh38.p7	9:33302547	TTTTTTTTTTTGAGA[C/T]GGTCTGCTGTGTTGC	4799
rs115749124	snp	C/T	0.021333	0.101051	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33353362	AGCCTCCTGAAGTCT[C/T]GGGACCTGTGTAGCC	4799
rs115754671	snp	A/G/T	0.0174175	0.0916809	intron-variant	NFX1	GRCh38.p7	9:33329629	CTGGTGAAAGCCTGG[A/G/T]TGGTTTTTATTTTTC	4799
rs115758295	snp	C/T	0.0168055	0.0901129	intron-variant	NFX1	GRCh38.p7	9:33316057	TTTTCCAGACTAAAA[C/T]TTCTGGTCTGTTCTC	4799
rs115831329	snp	G/T	0.00993419	0.0697739	intron-variant	NFX1	GRCh38.p7	9:33296154	CTAGTCTCAAACTTC[G/T]GACCTCGGGTGATCC	4799
rs115836298	snp	C/T	0.0111196	0.0737302	intron-variant	NFX1	GRCh38.p7	9:33356729	TGAATATCCATTTGA[C/T]GAGTACCAAGATTGT	4799
rs115864484	snp	A/G	0.0232847	0.105357	intron-variant	NFX1	GRCh38.p7	9:33311966	ATCTGGCATCTAAGA[A/G]TCTTTTAATGAATAT	4799
rs116011624	snp	A/G	0.0217236	0.101931	intron-variant	NFX1	GRCh38.p7	9:33306251	CTGTAGTTTTTGAGC[A/G]TGTGTGACTCTGACA	4799
rs116196461	snp	C/T	0.0479149	0.147179	intron-variant	NFX1	GRCh38.p7	9:33317343	AACATTGCTTGAGCC[C/T]GGGAGTTTGAGGCTG	4799
rs116238815	snp	A/G/T	0.0217236	0.101931	intron-variant	NFX1	GRCh38.p7	9:33340824	TTGCCACTCTCTTTG[A/G/T]TAAACAACAAGAGTC	4799
rs116311556	snp	G/T	0.0126979	0.078662	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352979	CGCCCTGTTTCCCAG[G/T]CTGGTCTCCCACCTT	4799
rs116437144	snp	C/T	0.0174175	0.0916809	intron-variant	NFX1	GRCh38.p7	9:33305601	ATTTTGGAGCCTAAA[C/T]AATTTGGGACTTATA	4799
rs116541890	snp	A/G	0.00438332	0.0466095	intron-variant	NFX1	GRCh38.p7	9:33332805	TAATGGTAGAATCTA[A/G]ATATGGGCATATGGA	4799
rs116580996	snp	C/T	0.00795532	0.062565	intron-variant	NFX1	GRCh38.p7	9:33300664	AGGATTATTCTGATA[C/T]TACACACTGGTCTGT	4799
rs116636847	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33346566	GAGCCCAGACGAGAG[C/T]GTGGTAGCCAAGGAA	4799
rs116691891	snp	C/T	0.021333	0.101051	intron-variant	NFX1	GRCh38.p7	9:33330783	AAAGCTATGTGTAAG[C/T]TGAATTTTTGCAAGT	4799
rs116709261	snp	A/T	0.0256215	0.110247	intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33350709	AAAATACAGCTTTTA[A/T]GCTGGATGCAGTGGC	4799
rs116862346	snp	C/T	0.00874735	0.0655527	intron-variant	NFX1	GRCh38.p7	9:33308382	AGGAGTTCACGGCTG[C/T]AGTGAGCTGTGATTG	4799
rs116902664	snp	A/G	0.00279162	0.0372561	intron-variant	NFX1	GRCh38.p7	9:33293007	CCTAGAATTCTGCCT[A/G]TGTGAAAGCTTTCAG	4799
rs116976364	snp	A/G	0.000399281	0.0141238	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294735	TGAGGAATGAGAAGC[A/G]CCATATCAGAGTCAA	4799
rs117053842	snp	C/G	0.00795532	0.062565	intron-variant	NFX1	GRCh38.p7	9:33298371	GGCAGGAAAGGTGGT[C/G]AGAGAAATAGCAAGG	4799
rs117083431	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33315891	TACCCACCTCTGTCT[A/C]AAAAAAAAAAAAGTG	4799
rs117211957	snp	A/G	0.00993419	0.0697739	utr-variant-3-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33370207	GGTCACTAGGTATGC[A/G]ATCACGCATTCAAAG	4799
rs117407683	snp	C/T	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33325029	GTGGGACACCTTTAA[C/T]TGTATCAGTGTACAT	4799
rs117463912	snp	A/C	1.65438e-05	0.00287605	intron-variant	NFX1	GRCh38.p7	9:33328556	TTGCAGTTTTCATTT[A/C]CAGCTCTTTTCGTTT	4799
rs117499155	snp	A/G	0.00438332	0.0466095	intron-variant	NFX1	GRCh38.p7	9:33321078	ATCAAATCCCCTTTC[A/G]GAAAGCACATGAGTC	4799
rs117607213	snp	C/T	0.00835141	0.0640778	intron-variant	NFX1	GRCh38.p7	9:33335751	TCTGCTTTCTATCTG[C/T]ATGGATTTACTATTT	4799
rs117628167	snp	A/T	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33370462	CTGAAATACCAAATA[A/T]TGAATTGGTATACCA	4799
rs117739333	snp	C/T	0.031825	0.122064	intron-variant	NFX1	GRCh38.p7	9:33341844	AAATAAGGCTGGATG[C/T]GGTGGCTCATGCCTG	4799
rs117783812	snp	A/G	0.0138799	0.0821421	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33365290	AAAAAGAAAGAAAGA[A/G]AGAAAGAAAGCTCTG	4799
rs117802651	snp	C/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33321749	CTGGGTATGGCGGCA[C/T]GTGCCTGTGGTCCCA	4799
rs117847114	snp	C/G	0.0023933	0.0345097	intron-variant	NFX1	GRCh38.p7	9:33316294	AGAAAAGCTCTCTAT[C/G]CTGGTACTTACCAAG	4799
rs117865697	snp	C/T	0.00358779	0.0422022	downstream-variant-500B	NFX1	GRCh38.p7	9:33371210	TTTCATTTTTTTTCC[C/T]CAATCCTCCTCCTCC	4799
rs117879808	snp	A/T	0.02016	0.0983543	intron-variant	NFX1	GRCh38.p7	9:33306938	ATTAGTCAAGATAGT[A/T]TTTTCGTAAGTAAAA	4799
rs118036898	snp	C/T	0.0023933	0.0345097	intron-variant	NFX1	GRCh38.p7	9:33356946	ACAGTGAGCCATGAT[C/T]ACCAGTCTGGACTAT	4799
rs137867798	snp	C/T	0.000399281	0.0141238	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33295077	CTAGAAAAGGAGTAT[C/T]GGATGGGTATGGAGC	4799
rs137901689	snp	A/G	0.00242181	0.0347137	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33364733	AAGTTTGTCAGTGAC[A/G]TTGAGAAGGAAATGG	4799
rs137904960	snp	A/G	0.0023933	0.0345097	intron-variant	NFX1	GRCh38.p7	9:33337083	GGTCTCATTATGTTG[A/G]CCAGGCTGGTCTCAA	4799
rs137932885	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33300892	CTTTCTAACCTAAAT[C/G]CATGGATCTGATAGA	4799
rs137968719	snp	A/G	1.64738e-05	0.00286995	splice-acceptor-variant	NFX1	GRCh38.p7	9:33318730	AAATTTTCTCTTCAA[A/G]TATGCTATTGCGGCA	4799
rs138032838	snp	A/C	0.000560843	0.0167364	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294638	GGAAGCAAACCTAAG[A/C]GTCAGCAGACGTCTT	4799
rs138036626	snp	A/T	0.0341408	0.126114	intron-variant	NFX1	GRCh38.p7	9:33333944	GAGGTCAGGAGTTCA[A/T]GGCCAGCCTAGCCAA	4799
rs138042477	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33367868	ATTTCCATGGTGTAG[A/G]TGGTGACACTGGGAA	4799
rs138099404	snp	C/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33326187	GGAGGCCAAGGTGGG[C/T]AGATCACTTGATGTC	4799
rs138099956	snp	C/T	0.000263596	0.0114773	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33319003	GCTGGTGCGCTGTTG[C/T]CCCTGTGGCCAAACT	4799
rs138155460	snp	G/T	0.00398564	0.0444627	intron-variant	NFX1	GRCh38.p7	9:33363013	CCAGCCTAAGTTCTC[G/T]TGTTCTATGGCACAC	4799
rs138157466	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33323430	AGATGTCAGATTTCA[C/T]AAAGACTGTAGGATA	4799
rs138172031	snp	A/G	0.00318978	0.0398085	intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33350602	AACAGGGATTATTAA[A/G]TAAAGTTAAGGTTTG	4799
rs138192163	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33310599	AGCATGCCTCCCCTC[A/G]TGTCAGCCTTCTTTT	4799
rs138214743	in-del	-/A			intron-variant	NFX1	GRCh38.p7	9:33324770	GTCTCTACTATATAC[-/A]AAAAAAAAATTAGCC	4799
rs138260842	snp	A/G	0.000328319	0.0128083	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33364744	TGACGTTGAGAAGGA[A/G]ATGGAAACCCTCGTG	4799
rs138289400	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33346686	ATTAATAGCAAAGAT[A/G]TCTGAGCAGAAGTGA	4799
rs138386675	snp	A/G	0.00517822	0.0506191	intron-variant	NFX1	GRCh38.p7	9:33301825	GCCTGTAATCCCAGC[A/G]CTTTGGGAGGCCAAG	4799
rs138409735	snp	A/G	0.0142736	0.0832652	intron-variant	NFX1	GRCh38.p7	9:33343112	TGCTACATGCCTCAT[A/G]TGTGTTATTGACCTA	4799
rs138462832	snp	A/C	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33304791	GAATATACTACCAGA[A/C]AGGCAGCATGAAACT	4799
rs138464568	snp	C/T	0.0162398	0.0886349	intron-variant	NFX1	GRCh38.p7	9:33334516	AAATTAATACACTTA[C/T]GAAGTTTAAAAAAAA	4799
rs138490530	in-del	-/A	0.00398564	0.0444627	intron-variant	NFX1	GRCh38.p7	9:33323968	TTCATTAGGCTGGGT[-/A]ACCGTGGCTTATGCC	4799
rs138495653	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33345874	CATCACTCAATTTCC[A/G]TATCTGTCAAGTCTA	4799
rs138587094	snp	C/T	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33367411	ATACCAGAGAGTGCT[C/T]AGTAGTGTCATAGTG	4799
rs138626481	snp	A/G	0.0023933	0.0345097	intron-variant	NFX1	GRCh38.p7	9:33317845	GCTGGGCGTGGTGGC[A/G]GGCCCCTATAATCCC	4799
rs138640111	snp	C/T	0.00279162	0.0372561	intron-variant	NFX1	GRCh38.p7	9:33294182	GTGAGCATTTTTACT[C/T]GACAACACTTAGCTG	4799
rs138664171	snp	A/G	0.00478085	0.0486577	intron-variant	NFX1	GRCh38.p7	9:33354593	CATAACAGAGAGGCC[A/G]TCATCCCACCTGTCC	4799
rs138759567	snp	A/G	0.0479149	0.147179	intron-variant	NFX1	GRCh38.p7	9:33334087	GAGACAGAGGTTGCA[A/G]TGAACTGAGATCACA	4799
rs138770253	snp	A/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33346405	AAGAGAAAAATACCC[A/T]GTGACCTTGAGGTTC	4799
rs138778215	snp	A/G	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33330418	TTACAAAAGTTGTGT[A/G]ATCATATATGGGTTT	4799
rs138868845	snp	C/T	3.295e-05	0.00405881	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33318922	CAGGGACTTGAAATG[C/T]GGTAACCATACATGT	4799
rs138880149	snp	C/G	0.000346984	0.0131671	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33295014	ATGCTGGACCCGAAA[C/G]TACCAAACCTGTGGG	4799
rs138964680	snp	G/T	0.0115144	0.0749975	intron-variant	NFX1	GRCh38.p7	9:33305459	AGTGGGAGATGACTG[G/T]AAAGGAAGGGCTGAC	4799
rs139033635	snp	C/T	0.0166325	0.0896639	intron-variant	NFX1	GRCh38.p7	9:33311706	TACAGGCGCCTGCCA[C/T]CGCACCTGGCTAGTT	4799
rs139071252	snp	A/G	0.00597247	0.0543191	intron-variant	NFX1	GRCh38.p7	9:33313567	CTTAGTGGGTTTTGA[A/G]GGGAGAGTTAGGGGC	4799
rs139109481	snp	C/G	0.0134861	0.0810011	intron-variant	NFX1	GRCh38.p7	9:33326687	TCATGCCACTGCATT[C/G]CAGCCTGAGTGACAA	4799
rs139113603	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33322200	AGTGAGACTCCATCT[C/T]GAAAAAAAAAAAAAA	4799
rs139155265	snp	A/C	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33355136	TAAACATCACATAAC[A/C]CAGCATACTTATTCA	4799
rs139177803	snp	A/C	0.00199481	0.0315187	intron-variant	NFX1	GRCh38.p7	9:33317221	CCCAGGAGTTTGAGA[A/C]CAGCTTGGGCAACAT	4799
rs139304421	snp	A/T	0.00597247	0.0543191	intron-variant	NFX1	GRCh38.p7	9:33368362	TTTGAATAATTTTTA[A/T]AACAAACATATTCAT	4799
rs139309095	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33302318	GTTGTTAGCCATAGT[A/G]CTACTAAACACTAGA	4799
rs139354210	snp	C/T	0.00716266	0.059414	intron-variant	NFX1	GRCh38.p7	9:33369255	TATTTTTAGTAGAAA[C/T]GGGGTTTCACCATGT	4799
rs139419866	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33356290	TCATTTTTGAAGTGC[C/T]TGTACAAGTCCTTTG	4799
rs139424941	snp	C/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33332596	TGTATTTGTCAAAAT[C/T]CAGTGAAGGCATACT	4799
rs139468485	in-del	-/TT	0.00835141	0.0640778	intron-variant	NFX1	GRCh38.p7	9:33307795	TTCTTTCTTTCTTTC[-/TT]TTTTTTTTTTTTTTT	4799
rs139491428	snp	A/T	0.00358779	0.0422022	intron-variant, utr-variant-3-prime	NFX1	GRCh38.p7	9:33348185	GAGACCCCCCCCATC[A/T]CTACTAAAATAATTA	4799
rs139565082	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33306862	CAATTCGCATATCAG[G/T]TCAGAAGTCCAGTTA	4799
rs139566763	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	NFX1	GRCh38.p7	9:33371436	GTGGGTGAATAGTAC[A/G]TGTGAGAGTATCTCA	4799
rs139574808	snp	A/G	3.29625e-05	0.00405958	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33319104	GAAAAGTGTGCGGCA[A/G]GCCTCTGCCTTGTGG	4799
rs139580602	snp	A/G	0.00993419	0.0697739	intron-variant	NFX1	GRCh38.p7	9:33337650	GGGAGGCTCATTTGA[A/G]TGCAGGAATTCGAGG	4799
rs139634183	snp	C/G	1.64773e-05	0.00287026	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33295318	CAACAAGTCTTCCAG[C/G]AGGGTTGACCAAGAG	4799
rs139651471	snp	A/G	0.00438332	0.0466095	intron-variant	NFX1	GRCh38.p7	9:33344412	AACACACCTAAAAAC[A/G]TTGGAAGACTCCCCA	4799
rs139687818	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33338229	GTGTGGTGGCAGGCA[C/T]CTGTAAGCCCAGCTA	4799
rs139726156	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33306551	AGGCCATGGACTGGG[A/G]ATGGCTGCAATTTAG	4799
rs139759458	snp	C/T	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33297080	TCAAGTTTTATCCTC[C/T]GGAGCAGCATAGTAA	4799
rs139791512	snp	C/T	0.00120265	0.0244924	intron-variant, missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33347679	AGTCCCACTACTGGG[C/T]GTCTACCCAGAAGAA	4799
rs139845933	snp	A/G	0.0248432	0.108648	intron-variant	NFX1	GRCh38.p7	9:33323702	AGGTTGCAGTGAGCC[A/G]CGATTGCGCCACTGC	4799
rs139874332	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33334712	CTAATATCTCAAAGA[C/T]GTATTTCCATGTCAG	4799
rs139879652	snp	A/G	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33319549	GAGTCTCGCTCTGTC[A/G]CCCCAGCTCGAGTGC	4799
rs139936652	snp	C/T	0.0181378	0.0934876	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352452	AGGGGGCATTGTGGA[C/T]GGGGCAATTCTTTCC	4799
rs140009891	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33299168	CAGACTGCCTTTGTT[A/G]AAACTAAGAAATTAG	4799
rs140042129	snp	C/T	0.0479149	0.147179	intron-variant	NFX1	GRCh38.p7	9:33302053	CTCCAGCCTGGGTGA[C/T]AGAGCAAGACCCTGT	4799
rs140087729	snp	C/T	0.0115144	0.0749975	utr-variant-3-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33370239	GGCTCTTTACACCAT[C/T]ACTGTGATTGCTCTG	4799
rs140104845	in-del	-/TAAA			intron-variant	NFX1	GRCh38.p7	9:33341806	CATAACCCGGTCTCT[-/TAAA]AAATAAATAGATTTA	4799
rs140178544	snp	A/G	1.68536e-05	0.00290285	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294474	CTCAGGAGAAAAAAA[A/G]TTCTGGTCTAAATTG	4799
rs140227150	snp	A/G	0.00358779	0.0422022	intron-variant, utr-variant-3-prime, downstream-variant-500B	NFX1, LOC105376018	GRCh38.p7	9:33348689	TTTGTAAAAAATGTG[A/G]TATCTATGAAATGCA	4799
rs140260224	snp	A/G	0.00478085	0.0486577	intron-variant	NFX1	GRCh38.p7	9:33345795	GTCTTGTGTTGCTGG[A/G]CATTTTAGTGTTTTC	4799
rs140401733	snp	A/G	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33333883	AGCCTGGTGGCTCAT[A/G]CCTGTAATCCCAGCA	4799
rs140506077	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33362532	AGACAGACACCACAC[A/G]ATCTCACTCATATGT	4799
rs140566514	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33343995	CAAAAATGTGTGTGT[G/T]TGTGTGTGTTAGTAT	4799
rs140574580	snp	A/G	0.00914312	0.0669923	intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33350028	AACAAAACAGGCCAG[A/G]CGTGGTTTCTCATGC	4799
rs140631750	snp	C/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33338722	GCAGCAGTCAGAGAG[C/T]TCTCATAGTCCCCAT	4799
rs140686211	snp	C/T	0.0103295	0.0711199	intron-variant	NFX1	GRCh38.p7	9:33341664	AGCCAGGCATTGTGG[C/T]TCACACCTGTAATTC	4799
rs140790123	snp	A/G	0.000691677	0.0185839	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33313698	CAGTCCACTGTTCTA[A/G]CCCATGTGAGAATAT	4799
rs140817809	snp	C/T	0.00279162	0.0372561	intron-variant	NFX1	GRCh38.p7	9:33293761	TTAATTTTTTCCACT[C/T]TGGGATTGTAGACCA	4799
rs140820791	snp	G/T	0.00199481	0.0315187	intron-variant	NFX1	GRCh38.p7	9:33336772	TGCCCTTTGCTTAAT[G/T]AACTTTTAATTAAGT	4799
rs140903869	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33361435	CACATTCTTATTTTT[A/G]GGGGGGTGAGACAAT	4799
rs140931627	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33317734	TAGTCCCAGCCCTTT[C/G]GGAAGCTGAGGCAGG	4799
rs140981123	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33327199	AGTTTTGATTTATTT[A/G]TTTTTTATAGAGGTG	4799
rs140982709	in-del	-/C			intron-variant	NFX1	GRCh38.p7	9:33310553	TCTTTCCATGACCCC[-/C]TTCCCTTTCATTCTC	4799
rs141001167	snp	G/T	0.0023933	0.0345097	intron-variant	NFX1	GRCh38.p7	9:33329300	TGTGTTCAGTTTTTA[G/T]TGGTGCTCTATTGTG	4799
rs141128443	snp	C/T	0.037233	0.131264	intron-variant	NFX1	GRCh38.p7	9:33366790	GTAGGTCAATCCCGC[C/T]GTCAGAGGAAGAACT	4799
rs141176897	snp	A/G	0.00436	0.0464865	intron-variant	NFX1	GRCh38.p7	9:33294370	GAGTCTATGAGTTTC[A/G]TGGATGAAGTTTAAT	4799
rs141189354	in-del	-/GGGGGGTG	0.239902	0.249796	upstream-variant-2KB	NFX1	GRCh38.p7	9:33289484	ACTGTGTGTGGGTCT[-/GGGGGGTG]GGGGGGTGGGGAGAA	4799
rs141198855	snp	A/C	0.000798403	0.0199641	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33366546	TCTTATTGATCCCTG[A/C]AATTCTTGTGTGGTA	4799
rs141206499	snp	C/T	0.00199481	0.0315187	intron-variant	NFX1	GRCh38.p7	9:33364437	CCAGTCTCACATTCA[C/T]ATGCGTTCTCAGTTG	4799
rs141264250	snp	C/T	0.110872	0.20771	intron-variant	NFX1	GRCh38.p7	9:33362806	CCTCCCGGGTTCAAG[C/T]GATTCTCCTGCCCCA	4799
rs141288436	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33326517	TGAGGCTAGGAGTTC[A/G]AGGCCAGCCTGGGCA	4799
rs141302578	snp	C/G			intron-variant	NFX1	GRCh38.p7	9:33292562	GCTACTTGAAATAGT[C/G]AAATAAAAATGGTGC	4799
rs141333079	snp	C/T	0.0003954	0.014055	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33318939	GTAACCATACATGTT[C/T]GCAAGTGTGCCACCC	4799
rs141337735	snp	A/G	0.0023933	0.0345097	intron-variant	NFX1	GRCh38.p7	9:33345965	GGCAAACCTGAAGTA[A/G]TTCAGGGGACCAGAT	4799
rs141377966	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33309022	GGAAGGAGTTAAGCT[A/G]TTCTTGCCATTAGTT	4799
rs141398955	snp	A/G	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33343716	ATCATTTGGAAAATA[A/G]TTCTTCACTGAGTTA	4799
rs141410248	snp	C/G	0.0023933	0.0345097	intron-variant	NFX1	GRCh38.p7	9:33302058	GCCTGGGTGACAGAG[C/G]AAGACCCTGTCTCAA	4799
rs141426893	snp	C/T	0.000164728	0.00907398	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33303228	CCCTGCCTGTCAGAA[C/T]GTTTCTGCACATGTT	4799
rs141437165	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33354346	TCTGCTCCATCCCCA[A/G]TGAATCCTACTCAGG	4799
rs141450310	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33300731	AACACCACCATGGGG[C/T]TTATGGTAGGCACCA	4799
rs141511995	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33309952	CACACCTGACAAGCA[A/G]TGAAAATTGTTTCAC	4799
rs141515778	snp	A/G	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33296408	TCTGTCACTCAGTTC[A/G]CTGACGAAGTCTTAC	4799
rs141576953	snp	C/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33368398	AAAGAGAAAAGAAAA[C/T]CAAGTTGGCAAGGGG	4799
rs141600641	snp	C/T	0.00993419	0.0697739	intron-variant	NFX1	GRCh38.p7	9:33324581	TTCATTAAAGGGGCT[C/T]AATAGTAGATTTGAG	4799
rs141645085	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33323704	GTTGCAGTGAGCCGC[A/G]ATTGCGCCACTGCAC	4799
rs141664476	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33322410	GATGGGGCTTCTTCT[C/G]CCCTCAGCTCCCAGT	4799
rs141687677	snp	A/G	0.0142736	0.0832652	intron-variant	NFX1	GRCh38.p7	9:33330793	GTAAGTTGAATTTTT[A/G]CAAGTAGAAGTCCTT	4799
rs141719350	snp	G/T			intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352210	TAATTATGGCTGTGG[G/T]GTCATGAGGGAGTAG	4799
rs141789477	snp	A/T	3.35329e-05	0.00409455	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33364102	ATAGTTTGAAAGAAG[A/T]TGCCAGGTATGTAAC	4799
rs141827607	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33306275	TCTGACAGAGTTGAC[A/G]TCACTGACAGAAATA	4799
rs141860211	snp	A/G	0.0115144	0.0749975	intron-variant	NFX1	GRCh38.p7	9:33358401	AGTGCTGGGATTACA[A/G]GCATGAGCCACTGCG	4799
rs141864148	snp	A/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33323249	TAGTCTAGCCAAGTC[A/T]CAAAACAAATAAATA	4799
rs141943031	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33300947	AATGCAAAGCAAGAT[C/T]CTGTATTGCCCAGTG	4799
rs142054340	snp	C/T	0.000798403	0.0199641	missense, nc-transcript-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33351731	GCTGACTGTGGTCAC[C/T]CGTGTATGGCACCCT	4799
rs142065044	snp	A/G	1.64727e-05	0.00286986	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33318769	CGAGATGTGTTATGT[A/G]GAACCGATGTAGGAA	4799
rs142078113	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33356193	TGTGTATAACAAGAT[A/G]TCATTGAGCTTTTAA	4799
rs142116030	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33337504	ATGGCTTCTCCTCCA[C/T]ACCTTAAACACTACC	4799
rs142151972	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33312741	CTGGGTGTGGTGACA[C/T]GTGCCTGTAGCCCCA	4799
rs142159623	snp	A/G	0.00478085	0.0486577	intron-variant	NFX1	GRCh38.p7	9:33320747	AAAAATGGAAAGTAG[A/G]CAACTGAGATTGAAT	4799
rs142165517	snp	G/T	0.00835141	0.0640778	intron-variant	NFX1	GRCh38.p7	9:33300333	CTCCCAAAGTGCTGG[G/T]ATTACAGGTGTAAGC	4799
rs142185123	snp	A/G	0.00159617	0.0282053	intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33351484	GCCATAAGCTTAGAA[A/G]TGTTTAAAGAGAAAG	4799
rs142255938	snp	C/T	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33342593	TTATCTTCATCCCCA[C/T]CTACTCTCCCTTCTG	4799
rs142322281	snp	A/G	0.0018601	0.0304399	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33295254	CAAAGGATGACCTCA[A/G]TGAAAGACCAGCAAA	4799
rs142345056	snp	A/G	0.00597247	0.0543191	intron-variant	NFX1	GRCh38.p7	9:33332995	GGATTACAGGTGTCC[A/G]CCACTACACCTGGCT	4799
rs142414854	snp	A/G	1.64808e-05	0.00287057	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33347061	TCTTGTCATAGTGAG[A/G]AGAAGTGTCCCCCTT	4799
rs142445916	snp	A/G	0.00398564	0.0444627	intron-variant	NFX1	GRCh38.p7	9:33353753	GAGTGCAATGGTGCA[A/G]TCTCGGCTCACTGCA	4799
rs142459232	snp	G/T	0.0103295	0.0711199	intron-variant	NFX1	GRCh38.p7	9:33355431	TTGAACTTTATGTAA[G/T]TGATGAAATCATGTA	4799
rs142572025	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	NFX1	GRCh38.p7	9:33348072	ACTACACACTGGGTC[C/T]GAGCACGGTGGCTCA	4799
rs142587929	snp	A/G	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33356730	GAATATCCATTTGAC[A/G]AGTACCAAGATTGTC	4799
rs142599751	snp	C/T	0.0199719	0.0979136	intron-variant, utr-variant-3-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33347776	AAAATGTGGAACCAG[C/T]CCAACTGCCCATCAG	4799
rs142676453	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33326200	GGCAGATCACTTGAT[A/G]TCAGGAGTTTGAGAC	4799
rs142685159	snp	C/T	0.0422008	0.138995	intron-variant	NFX1	GRCh38.p7	9:33334103	TGAACTGAGATCACA[C/T]CATTGCTCTCCAGCC	4799
rs142688728	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33336669	TGCAGTGGCAGACCA[C/T]AGCTCACTGCAGCCT	4799
rs142834033	snp	C/T	1.64895e-05	0.00287132	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33366640	ACAGGGAAAGAATAG[C/T]AAGAAAAGCCACAGC	4799
rs142858188	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33337684	CAGTGAGCTATGTTA[A/G]TGCTACTGCACTCCA	4799
rs142869109	snp	A/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33366421	CAGCTGCGACTGTTG[A/T]GGCTCACAGAGTAGG	4799
rs142903858	snp	A/G	1.65015e-05	0.00287237	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33319116	GCAAGCCTCTGCCTT[A/G]TGGTTCCTTAGGTAA	4799
rs142940288	snp	A/G	0.00199481	0.0315187	intron-variant	NFX1	GRCh38.p7	9:33328820	CAGAGGCCTATAGTG[A/G]GATAAGGCAAATATA	4799
rs142978308	snp	C/T	0.00199481	0.0315187	intron-variant	NFX1	GRCh38.p7	9:33317630	GTTCACACCACTGTA[C/T]TCCAGCTGGGCAACA	4799
rs142999387	snp	A/G	0.0267878	0.112589	intron-variant	NFX1	GRCh38.p7	9:33343179	TAGCAGCAGTTTGCA[A/G]ACTTTTTGGTTGTAG	4799
rs143045923	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33311846	ATGAGCTACCGCGCT[C/T]GGTCGGCAAGGATTT	4799
rs143076598	snp	A/G	0.00358779	0.0422022	intron-variant	NFX1	GRCh38.p7	9:33305028	GCACATAAAGGCCTT[A/G]TTTGCAGATGACTTT	4799
rs143111645	in-del	-/A			intron-variant	NFX1	GRCh38.p7	9:33322202	TGAGACTCCATCTCG[-/A]AAAAAAAAAAAAAAA	4799
rs143142263	snp	C/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33363350	AGTGTAGTGGCACAA[C/T]CTCGGTTCACTGCAA	4799
rs143201093	snp	A/G	0.0232847	0.105357	intron-variant	NFX1	GRCh38.p7	9:33314667	GGATGACAGAATGAG[A/G]CTCAGTCTAAAATAA	4799
rs143251638	snp	C/T	0.00953873	0.0683987	intron-variant	NFX1	GRCh38.p7	9:33325789	GCCTTACAGTAAGTA[C/T]TAAAAGAAATTCTTC	4799
rs143320370	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33349495	TATGGATTCCAGTGC[A/G]ATGGGAAATATGTAT	4799
rs143387337	snp	A/C	0	0	intron-variant	NFX1	GRCh38.p7	9:33337355	TAAGGGAGGGTGTGC[A/C]TAGGTTATATGCAAA	4799
rs143454591	snp	A/G	0.000119581	0.00773152	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33364849	AGCAATCAAGTCCTG[A/G]AAACACTTTCAACCT	4799
rs143491414	snp	C/T	0.00320747	0.039918	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33367589	CACGGCCTCCACCAC[C/T]GATTCCTCATCACAG	4799
rs143543780	snp	C/T	4.94303e-05	0.00497119	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33295312	AGTCATCAACAAGTC[C/T]TCCAGGAGGGTTGAC	4799
rs143548972	snp	A/C	0.00358779	0.0422022	utr-variant-3-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33370687	AACCTGTTCAGTAAC[A/C]ATCAGTTTGGCCGTC	4799
rs143559591	snp	C/G	0.000264828	0.0115041	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33354180	AAAAAGGAAGTTCAT[C/G]AAGCCAGGTAATTTT	4799
rs143592240	snp	C/G	1.65083e-05	0.00287296	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294646	ACCTAAGAGTCAGCA[C/G]ACGTCTTTCCAGTCC	4799
rs143617101	snp	A/G	0.000428343	0.0146283	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33366665	CACAGCTTCCCTCCC[A/G]TGAACAGAGACCACC	4799
rs143659134	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33293165	ACTGAGTTGGAACCC[C/T]GAGTCTTCCTTGGAA	4799
rs143668586	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33358068	TTTTGTATTCTTTCA[A/G]TAGATTTGTTTCTTG	4799
rs143743524	snp	A/C	0.0248432	0.108648	intron-variant	NFX1	GRCh38.p7	9:33315733	CTCTAACAACAACAA[A/C]AAAAAAAAATTAGCC	4799
rs143808423	snp	A/G	0.00398564	0.0444627	intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33350412	TATAAGAATTAGTCT[A/G]TTGACTCTGCTTTAG	4799
rs143874131	snp	C/T	0.00199481	0.0315187	intron-variant	NFX1	GRCh38.p7	9:33346755	TAGAATTGGATGGAC[C/T]ATATGGCTGTGCTGC	4799
rs143881330	snp	A/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33326812	TTCTAACAAAGTAGT[A/T]TTGGGTTTATAACAT	4799
rs143896389	in-del	-/T	0.273587	0.248885	intron-variant	NFX1	GRCh38.p7	9:33302379	TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTTAC	4799
rs143939428	snp	A/G	0.00199481	0.0315187	intron-variant	NFX1	GRCh38.p7	9:33296114	GTATTTTTAGTAGAA[A/G]TGGGGTTTCACCATG	4799
rs143967704	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33351942	AGGTAGAGTAAGTCA[C/T]ACAAGTTTCTGCCTG	4799
rs144003788	snp	C/G	0.000798403	0.0199641	intron-variant, downstream-variant-500B	NFX1, LOC105376018	GRCh38.p7	9:33349102	TTCTAAAACATCAAT[C/G]TGTTATCTTCGTACT	4799
rs144043679	snp	C/T	0.00331559	0.0405808	intron-variant	NFX1	GRCh38.p7	9:33313625	GAACTTTTACACTGA[C/T]GCTGTCTTTACATCT	4799
rs144117681	snp	A/G	0.000148288	0.00860943	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33318979	CCAGCAATGCCCACG[A/G]CTCCCCCAGCTGGTG	4799
rs144184873	snp	C/T	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33335481	CATGTAATCCGCCTG[C/T]CTCAGCCTCCCAAAG	4799
rs144219565	snp	G/T	0.00636936	0.0560724	intron-variant	NFX1	GRCh38.p7	9:33333189	CTGTTGTTGAAGCCA[G/T]TTTAAAACCTTTTTG	4799
rs144224895	snp	C/G	1.64773e-05	0.00287026	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33367600	CCACCGATTCCTCAT[C/G]ACAGACATCAGTCAG	4799
rs144229739	snp	C/T	0.000164875	0.00907801	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33295153	GGAAGTGGAGGGGGC[C/T]AGGCCACGACCAGGC	4799
rs144277865	snp	A/G	0.00517822	0.0506191	intron-variant	NFX1	GRCh38.p7	9:33343532	AAGAGTATTTTAAAG[A/G]TGTTTTCAAATAATT	4799
rs144345047	snp	C/T	0.0103295	0.0711199	intron-variant	NFX1	GRCh38.p7	9:33332974	CCTCAGCCTCCCAAG[C/T]AGCTGGGATTACAGG	4799
rs144361670	snp	A/G	3.29603e-05	0.00405944	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33295351	ATGCACTGTACGGAG[A/G]CAGGATCCTCAAGTA	4799
rs144462968	snp	A/C	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33297799	GAAAGCAGCTGCTGC[A/C]ACTTCAGATCTCTCT	4799
rs144519029	snp	C/T	0.000708116	0.0188031	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33344160	ATGTACCCAAACCTG[C/T]GCTAGAGTCCATGAG	4799
rs144522602	snp	A/G	0.00238571	0.0344552	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33318780	ATGTGGAACCGATGT[A/G]GGAAAGTCTGATGGA	4799
rs144651970	snp	C/T	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33346560	GTGAGGGAGCCCAGA[C/T]GAGAGTGTGGTAGCC	4799
rs144681736	in-del	-/AAAACAAAAC	0.478271	0.101943	intron-variant	NFX1	GRCh38.p7	9:33337732	AGACCCTGTCTCTTT[-/AAAACAAAAC]AAAACAAAACAAAAC	4799
rs144726964	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33306011	ACCCCAAAACATCAT[G/T]TGGAGTCAGGGACAA	4799
rs144730837	snp	C/T	0.00199481	0.0315187	intron-variant	NFX1	GRCh38.p7	9:33326296	CATATGCCTGTGATC[C/T]CAGCTACTCAGGAGG	4799
rs144787339	snp	A/G	0.000395329	0.0140538	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33367525	ATCAGGGGGAAGTCC[A/G]TTTGTCCTCCTACCA	4799
rs144790423	snp	A/C	0.0126979	0.078662	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33365157	CGGGCACCTGTTATT[A/C]CAGCTACTTGCAAGG	4799
rs144790540	snp	A/G	0.00597247	0.0543191	intron-variant	NFX1	GRCh38.p7	9:33301743	CAGAAGTGTGATTGC[A/G]GGATCATATGGTAAT	4799
rs144790876	snp	C/T	0.0197687	0.0974348	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33365126	TAAAAATATAAAAAT[C/T]AGCTGGGTGTGGTGG	4799
rs144830384	snp	A/T	0.00716266	0.059414	intron-variant	NFX1	GRCh38.p7	9:33291562	GACCATATATGTATT[A/T]GTATACTGGGTGGCA	4799
rs144876675	snp	A/G	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33329975	ATTTTTGTATTTTTA[A/G]TAGAGGTGGGGTTTC	4799
rs145038884	snp	A/G	0.00036053	0.0134214	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33369967	ATTGACTATTTTGAC[A/G]TCCAGGACTAAGAAG	4799
rs145070308	snp	A/G	0.00199481	0.0315187	intron-variant	NFX1	GRCh38.p7	9:33338676	TGGAGAATGCAGCCC[A/G]GATTTAAAAGTCACT	4799
rs145160044	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33309216	TAAAAAATTAGCCGG[A/G]TGTGGTGGTGGGCAC	4799
rs145199965	snp	C/T	0.0607341	0.163335	intron-variant	NFX1	GRCh38.p7	9:33336376	GCCCGCCACCGCGCC[C/T]GGCTAATTTTTGTAT	4799
rs145204863	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33308836	GTATTTCTACTGCTT[A/G]GAGGAGGGATAATAT	4799
rs145283370	snp	C/T	0.00557542	0.0525036	intron-variant	NFX1	GRCh38.p7	9:33324965	GATTATATAACCCAA[C/T]GGACAGAGAGAAAAT	4799
rs145299899	snp	A/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33306691	GATTTGCAGTGACAT[A/T]GATTATAAAAGTATA	4799
rs145308790	in-del	-/AAAA			intron-variant	NFX1	GRCh38.p7	9:33327081	GAGTATTAGAATAAC[-/AAAA]AAGACATGAGACTTA	4799
rs145313410	snp	C/T	0.00993419	0.0697739	intron-variant	NFX1	GRCh38.p7	9:33303491	GGCTCATGCTGCTTC[C/T]GGGCTGTAGTGCTTG	4799
rs145402920	snp	A/G	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33358462	TTATTATTATTTAAT[A/G]TGACAAGTGTTTTGT	4799
rs145430908	snp	A/C	0.0138799	0.0821421	intron-variant	NFX1	GRCh38.p7	9:33320389	ACTGTATTACACTGA[A/C]TGCAGTGGTGCCCTT	4799
rs145448405	snp	C/T	1.64844e-05	0.00287087	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33313657	TTGTCTTTACAGGCA[C/T]ACAGTTCGCTGTGGT	4799
rs145501352	snp	G/T	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33307440	GTCTCAAATCACCCT[G/T]TGCCAGGCACTCTAC	4799
rs145512211	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33356440	TTTTTTACTCTCTTG[A/G]TGCCTTTTTTTAATC	4799
rs145547738	snp	A/G	0.0115144	0.0749975	intron-variant	NFX1	GRCh38.p7	9:33362807	CTCCCGGGTTCAAGC[A/G]ATTCTCCTGCCCCAG	4799
rs145661265	snp	C/G	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33360208	AAGACATATTGTATA[C/G]TAGTTAGAGCCAGAG	4799
rs145748201	snp	A/G	0.00279162	0.0372561	intron-variant	NFX1	GRCh38.p7	9:33342692	CTTGTTGTTATTTAT[A/G]GAAAATATAAAATGA	4799
rs145753714	snp	A/G	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33299287	AATCCAGGATACCAC[A/G]TTGCATTTAGTCATG	4799
rs145766809	snp	A/G	0.00676609	0.0577691	intron-variant	NFX1	GRCh38.p7	9:33354590	CCCCATAACAGAGAG[A/G]CCATCATCCCACCTG	4799
rs145779406	snp	C/G	0.00676609	0.0577691			GRCh38.p7	9:33357414	TCTTAATTACTGTAC[C/G]TTTATAACAAGTCTT	4799
rs145785932	snp	A/G					GRCh38.p7	9:33368092	TATAAAAAAGTAGCC[A/G]GGTGTGGTGGCGGGC	4799
rs145853304	snp	A/G	0.00914312	0.0669923	intron-variant	NFX1	GRCh38.p7	9:33315628	GATTGGCCTGGGCAC[A/G]GTAGCTCATGCACTC	4799
rs145885236	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33353023	GCTGGGATCACAGGC[A/G]TGAGCCACTACACCT	4799
rs145891696	snp	C/G	0.00478085	0.0486577	intron-variant	NFX1	GRCh38.p7	9:33345820	GTTTTCAGTTTTCCT[C/G]TGATAAACTGCTCAG	4799
rs145900391	snp	C/T	0.000487678	0.0156077	missense, nc-transcript-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33351732	CTGACTGTGGTCACC[C/T]GTGTATGGCACCCTG	4799
rs145934546	in-del	-/TTTTA	0.49719	0.0373808	intron-variant	NFX1	GRCh38.p7	9:33354073	CTTTTTCCCTTTCTT[-/TTTTA]TATTTCAGAATAGCT	4799
rs145964114	snp	C/T	0.00199481	0.0315187	intron-variant	NFX1	GRCh38.p7	9:33319258	TTATGATCATATTTA[C/T]GTAGGTACGTTTTCT	4799
rs145982467	snp	A/G	0.204189	0.245767	intron-variant	NFX1	GRCh38.p7	9:33355763	GATTCTCTTGCCTTA[A/G]CCTCCAGAGTAGTTG	4799
rs146008373	snp	A/G	0.0337553	0.125452	intron-variant	NFX1	GRCh38.p7	9:33336828	TTTCCAGGGCTGGGC[A/G]CAGTAGCTCACGCCT	4799
rs146084424	snp	C/T	0.00159617	0.0282053	utr-variant-3-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33370212	CTAGGTATGCAATCA[C/T]GCATTCAAAGAGGCT	4799
rs146117232	snp	A/G	3.29451e-05	0.00405851	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33344103	CCATTGTGGTGCATC[A/G]GTGATTTACCCTCCA	4799
rs146128133	in-del	-/CT	0.0422008	0.138995	intron-variant, utr-variant-3-prime	NFX1	GRCh38.p7	9:33348018	AATGGACTTTGGGGA[-/CT]CTCTGGGGAAAGGAC	4799
rs146161975	in-del	-/TA			intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33353425	TAGAGAATGAATGGT[-/TA]TATATATATATATCT	4799
rs146206603	snp	C/T	8.24572e-05	0.00642042	synonymous-codon, nc-transcript-variant	NFX1, LOC105376018	GRCh38.p7	9:33351577	TCGGAGCAACATCCC[C/T]TGTCACCTGGTTGAT	4799
rs146247251	snp	G/T	0.0111196	0.0737302	intron-variant	NFX1	GRCh38.p7	9:33354724	ACAGGCTGCTTCCTG[G/T]CCTGAGGGATTGTTT	4799
rs146278102	snp	C/T	0.0170251	0.090679	intron-variant	NFX1	GRCh38.p7	9:33353923	ATGAACTCCTGACCT[C/T]AGGTGATCCACCTGC	4799
rs146305609	snp	C/T	1.64746e-05	0.00287002	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33319055	CTTGGAAGTAGTAGT[C/T]GGAAAACATGCATGG	4799
rs146369956	snp	C/T	0.00199481	0.0315187	intron-variant	NFX1	GRCh38.p7	9:33337612	GCTTACACCTGTAAT[C/T]CCAACATTTGGAAGG	4799
rs146425876	snp	A/C/T	0.00478085	0.0486577	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352003	GGTACCCACTGCCAC[A/C/T]GGACCACAGTCTGTG	4799
rs146470023	snp	C/T	0.000758387	0.0194581	intron-variant	NFX1	GRCh38.p7	9:33313648	TTACATCTATTGTCT[C/T]TACAGGCACACAGTT	4799
rs146508853	snp	A/G	0.0278271	0.114626	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33366684	ACAGAGACCACCGCC[A/G]GATCATCCATGACTT	4799
rs146531998	snp	A/C/G			intron-variant	NFX1	GRCh38.p7	9:33356991	AGTGAAATGCTGTCT[A/C/G]AAAAAAAAAAAAAAA	4799
rs146533250	snp	C/T	0.00597247	0.0543191	intron-variant	NFX1	GRCh38.p7	9:33292545	CTGTTTACTAACTTC[C/T]AGCTACTTGAAATAG	4799
rs146536904	snp	A/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33316667	AGCCTTATCTAGAGA[A/T]TAATAAGCATTCTTT	4799
rs146608484	snp	A/G	0.000153988	0.00877328	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33301397	TGCATAAAGAAATGG[A/G]CAAGGTCTCCAGCAT	4799
rs146627477	snp	C/T	0.000798403	0.0199641	intron-variant, downstream-variant-500B	NFX1, LOC105376018	GRCh38.p7	9:33349147	ACTTCATTCAACAGA[C/T]ATCGAGTATGAGTAC	4799
rs146666723	snp	A/G	0.0130921	0.0798413	intron-variant	NFX1	GRCh38.p7	9:33345459	TCCAGCCTGGGTGAC[A/G]GAGTGAGACTCTGTC	4799
rs146707947	snp	C/T	0.00318978	0.0398085	intron-variant, utr-variant-3-prime, downstream-variant-500B	NFX1, LOC105376018	GRCh38.p7	9:33348383	TTTAAAAACTACACA[C/T]TGGGTACAATGTACA	4799
rs146747849	snp	C/T	0.00636936	0.0560724	intron-variant	NFX1	GRCh38.p7	9:33333190	TGTTGTTGAAGCCAT[C/T]TTAAAACCTTTTTGG	4799
rs146788753	snp	C/T	0.0023933	0.0345097	downstream-variant-500B	NFX1	GRCh38.p7	9:33371207	TCTTTTCATTTTTTT[C/T]CCTCAATCCTCCTCC	4799
rs146789262	snp	C/T	0.00478085	0.0486577	intron-variant	NFX1	GRCh38.p7	9:33329829	ACACCCGGCTAATTT[C/T]TGTATTTTTAGTAGA	4799
rs146828525	snp	C/T	0.00398564	0.0444627	intron-variant	NFX1	GRCh38.p7	9:33321013	TCATCTGTTGGTTCT[C/T]TGCTTGCCATGAAAA	4799
rs146919774	snp	C/T	0.0134861	0.0810011	intron-variant	NFX1	GRCh38.p7	9:33336959	ATACAAAAAATTAGC[C/T]GGCATGGTGGCAGGC	4799
rs146955754	snp	A/G	0.021333	0.101051	intron-variant	NFX1	GRCh38.p7	9:33340276	GATTTCTGTGCACCC[A/G]CAGGCTCAGCACCAC	4799
rs147128081	snp	A/G	0.00517822	0.0506191	intron-variant	NFX1	GRCh38.p7	9:33331216	CTCATTGTTTAACTA[A/G]ATTTTTCATGAATAT	4799
rs147166092	in-del	-/T			intron-variant	NFX1	GRCh38.p7	9:33316312	GGTACTTACCAAGCC[-/T]TTTTTTTTTTTTTTG	4799
rs147195056	snp	A/G	4.9731e-05	0.00498629	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294759	GAGTCAAGAAAGCAC[A/G]GAGTCTTGCTGAGCA	4799
rs147215181	snp	C/T	0.00438332	0.0466095	intron-variant	NFX1	GRCh38.p7	9:33312636	AGCATTTCGGGAGGC[C/T]GAGGTGGGTGGATCA	4799
rs147224491	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33358365	TCCTGACCTTATGAT[C/T]TGCCCGCCTCAGCCT	4799
rs147250148	snp	A/G	0.0103295	0.0711199	intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33350588	TCCTTTTGAGTCATA[A/G]CAGGGATTATTAAAT	4799
rs147336848	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33361217	AGAAGACTATGAGCC[A/G]TGAAGACAGTTAAGT	4799
rs147389628	snp	C/T	0.00636936	0.0560724	upstream-variant-2KB	NFX1	GRCh38.p7	9:33289559	CAGGAAAGCCAAAGA[C/T]AGGGTTGTGCCTTAC	4799
rs147463103	snp	A/G	0.00478085	0.0486577	intron-variant	NFX1	GRCh38.p7	9:33317792	ACCAGCCTGGCCAAC[A/G]TGGTGAAACTCCATC	4799
rs147531914	snp	C/T	0.0023933	0.0345097	intron-variant	NFX1	GRCh38.p7	9:33332163	CTTTCCTTTGCATGC[C/T]TTTAGCAGCCCTCTT	4799
rs147558152	snp	A/G	0.000148249	0.00860829	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33367560	GACAGGTGTGCTTGA[A/G]AGGGAAATGCAGGCA	4799
rs147638230	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33303764	AATATCTCAGTTCCC[C/G]CAAGTATTAGGGGAA	4799
rs147654156	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33306699	GTGACATTGATTATA[A/G]AAGTATAAGGTCTTT	4799
rs147721031	snp	A/C	0.00358779	0.0422022	intron-variant	NFX1	GRCh38.p7	9:33356550	TTAATAAGCACTTTT[A/C]ATGTCCTATTTAGAA	4799
rs147789098	snp	A/C	0.000153988	0.00877328	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33369908	GTTTGTTTTTCAGGA[A/C]TCCTGGGAGCAGTAA	4799
rs147790122	snp	C/T	0.0256215	0.110247	intron-variant	NFX1	GRCh38.p7	9:33336856	CCTGTAATCCCAGCA[C/T]TTTGGGAGGCCAAGG	4799
rs147818472	snp	A/G	0.000214177	0.0103461	missense, nc-transcript-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352684	ACGAAGAAAAGAGAT[A/G]GTGATTTGCTCTGAA	4799
rs147828912	snp	A/G	0.0256215	0.110247	intron-variant	NFX1	GRCh38.p7	9:33302882	ATCATGTTAGCCAGG[A/G]TGGTCTCAATCTCCT	4799
rs147861913	snp	C/T	3.29516e-05	0.00405891	intron-variant	NFX1	GRCh38.p7	9:33344196	CCATCCAGGTGAGTA[C/T]CAACTTGTCTTCACA	4799
rs147969277	snp	A/G	0.00676609	0.0577691	intron-variant	NFX1	GRCh38.p7	9:33328060	CTGTCACCTAGACTG[A/G]AGTTCAGTGGTGCGA	4799
rs147998917	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33330549	GAGATGCTGTGATTT[C/G]GCAATCATAAATTTA	4799
rs148050291	snp	C/T	3.31411e-05	0.00407056	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33364062	GATCCTTTCAATATA[C/T]GTTCTTCAGGGTCAA	4799
rs148087720	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33322631	TCACCCCAGCTCACT[C/T]GTAGGGCAGAGGTTC	4799
rs148157154	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33334511	ATACAAAATTAATAC[A/G]CTTATGAAGTTTAAA	4799
rs148209983	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33363669	AACATTTGTATGTCT[A/G]TTTTATGTACCTTAT	4799
rs148263704	snp	C/G	0.0126979	0.078662	intron-variant	NFX1	GRCh38.p7	9:33358209	GGCTCACTGCAAGCT[C/G]CACCTCCCGGGTTCA	4799
rs148298310	snp	A/C	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33354020	AGAGGTCTTCTGTAT[A/C]CCAAGTATAAGGAGG	4799
rs148344677	in-del	-/AAAT			intron-variant	NFX1	GRCh38.p7	9:33323779	CAAACAAAAAAAAAC[-/AAAT]AAATAAATATCTTCA	4799
rs148351114	snp	C/T	0.0107246	0.0724382	intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33349611	TAGCCTTTGGTCCTA[C/T]GAGAGTAAAATTTCA	4799
rs148359129	snp	C/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33296328	ATCTACCACATTTTA[C/T]TCCCTGGATTCTACA	4799
rs148384803	snp	C/T	0.00279162	0.0372561	intron-variant	NFX1	GRCh38.p7	9:33337443	GGTCCTGGAATCAGT[C/T]CCCCATGGACTCCAA	4799
rs148386757	snp	A/G	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33309695	TGCAGTGGTGCTATC[A/G]TAGCTCACTGCACCC	4799
rs148400878	snp	A/G	0.0023933	0.0345097	intron-variant	NFX1	GRCh38.p7	9:33323818	TTGAAGGGAAACCAT[A/G]CTTAAAGAGGTAAAG	4799
rs148454292	snp	C/T	1.64743e-05	0.00287	intron-variant	NFX1	GRCh38.p7	9:33318888	TATGCAACAATTATG[C/T]AATAGTGTGTTTTCT	4799
rs148521615	snp	C/G	0.00279162	0.0372561	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33365686	AGAAACTCTGGGTGA[C/G]GGGGCTCAATAGTGA	4799
rs148542425	snp	A/G	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33306127	TAGTCTGGAGATGAG[A/G]TTTTGGCCAGTTAGA	4799
rs148574249	snp	C/G	0.00676609	0.0577691	intron-variant	NFX1	GRCh38.p7	9:33360184	TGGAAATGTACTTTT[C/G]GTGGTTGAAAGACAT	4799
rs148608486	snp	A/G	0.0178098	0.0926698	intron-variant	NFX1	GRCh38.p7	9:33355937	AGCTTGAGCCACCAC[A/G]CCCAGCCCAGAACAT	4799
rs148661958	snp	G/T	0.00398564	0.0444627	intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33351142	ACAGAGTGAGACTTC[G/T]TCTCAAAATAAATAA	4799
rs148726750	snp	C/G	1.64781e-05	0.00287033	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33295238	AACATGGGCCCCATT[C/G]CAAAGGATGACCTCA	4799
rs148732200	snp	A/G	0.0260105	0.111035	intron-variant	NFX1	GRCh38.p7	9:33332987	AGTAGCTGGGATTAC[A/G]GGTGTCCACCACTAC	4799
rs148751170	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33343606	GAAAGGACTTGACTC[A/G]GTGTTTTTATTCTCT	4799
rs148777292	snp	C/T	1.64838e-05	0.00287083	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33347048	TGCAGTATATCATTC[C/T]TGTCATAGTGAGGAG	4799
rs148815959	snp	C/T	0.000659022	0.0181405	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33313664	TACAGGCACACAGTT[C/T]GCTGTGGTCAGGCTG	4799
rs148856222	snp	C/T	0.00636936	0.0560724	intron-variant	NFX1	GRCh38.p7	9:33307960	AGGCGTGTGCCACCA[C/T]GCCTGGCTAATTTTT	4799
rs148869668	snp	C/G	0.000153988	0.00877328	missense, nc-transcript-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352704	TTTGCTCTGAAGCAT[C/G]TAGTACTTATCAAAG	4799
rs148871493	snp	A/T	0.00398564	0.0444627	intron-variant	NFX1	GRCh38.p7	9:33330419	TACAAAAGTTGTGTA[A/T]TCATATATGGGTTTT	4799
rs148888179	snp	C/T	0.00455264	0.0474931	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33367551	TACCACGCTGACAGG[C/T]GTGCTTGAAAGGGAA	4799
rs148890850	snp	C/T	0.0221141	0.102801	intron-variant	NFX1	GRCh38.p7	9:33336480	CAGCCTCTCAAAGTG[C/T]TGGGATTACAGGCGT	4799
rs148923754	snp	C/T	0.00597247	0.0543191	intron-variant	NFX1	GRCh38.p7	9:33358066	AATTTTGTATTCTTT[C/T]AGTAGATTTGTTTCT	4799
rs148976573	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33353200	TTCTCTCTTTTGGTC[A/G]TATTACATTGTGAGA	4799
rs149005323	in-del	-/AAAAGA	0.499866	0.0081858	intron-variant	NFX1	GRCh38.p7	9:33345170	CCATCTCAAAAAAAG[-/AAAAGA]AAAAGAAAAAGAAAA	4799
rs149044690	snp	A/G	0.0023933	0.0345097	intron-variant	NFX1	GRCh38.p7	9:33304057	GGATCACCTGAGATC[A/G]GGAGTTCGACACCAG	4799
rs149064209	snp	A/G	0.00755907	0.0610114	intron-variant	NFX1	GRCh38.p7	9:33345199	AAGAAAAAAAAGGCC[A/G]GGTGCAGTGACTCAC	4799
rs149096674	snp	C/T	0.0252325	0.109451	intron-variant	NFX1	GRCh38.p7	9:33299757	TGAATTTAACAAATA[C/T]TTAATGGAGCACCTA	4799
rs149133904	snp	C/T	0.00398564	0.0444627	intron-variant	NFX1	GRCh38.p7	9:33325215	AATGCTAAAAGTTAA[C/T]GATAAGGAGAAAGTC	4799
rs149222595	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33349238	TTGCCCTTATGAAGC[C/T]TTCACTTTGGGTTAG	4799
rs149237096	snp	A/G	0.0248432	0.108648	intron-variant	NFX1	GRCh38.p7	9:33359551	GTGCAGTGAGCCGAG[A/G]TGGCGCCACCACACT	4799
rs149258577	snp	A/G	0.00438332	0.0466095	intron-variant	NFX1	GRCh38.p7	9:33301553	GAGTATGTTACCTTG[A/G]TCATGTGTTTCATAT	4799
rs149290040	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33354660	GTCCCTGGGGAAATG[A/G]TATTTCTAGGGCAAG	4799
rs149322800	in-del	-/TTTT	0.0275645	0.114116	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33353180	CCTCCTTCCTCTTTC[-/TTTT]TTTCTCTCTTTTGGT	4799
rs149326448	snp	C/T	3.29468e-05	0.00405861	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33318731	AATTTTCTCTTCAAG[C/T]ATGCTATTGCGGCAG	4799
rs149336198	snp	C/T	0.000560954	0.0167381	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33295081	AAAAGGAGTATTGGA[C/T]GGGTATGGAGCCAGA	4799
rs149341996	snp	A/G	1.64751e-05	0.00287007	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33319015	TTGCCCCTGTGGCCA[A/G]ACTCCTCTCAGCCAA	4799
rs149392456	snp	A/G	3.29598e-05	0.00405941	synonymous-codon, nc-transcript-variant	NFX1	GRCh38.p7	9:33366706	CCATGACTTGGCCCA[A/G]GTTTATGGCCTGGAG	4799
rs149416158	snp	C/G	0.00398564	0.0444627	intron-variant	NFX1	GRCh38.p7	9:33305736	GCTTTTGGAAATGGT[C/G]ATACCAAGGAAAAGG	4799
rs149450417	snp	C/T	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33326712	TGACAAGAGTGGGAC[C/T]CTGTCTCCAAAAATT	4799
rs149537971	snp	A/G	0.00318978	0.0398085	intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33350963	CCAGCCATCTGGCCA[A/G]CATGGCGAAACCCCA	4799
rs149591764	snp	C/T	0.00130151	0.0254767	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33311141	GCCCACCCTGCCCTG[C/T]CTTTATGACAAAAAC	4799
rs149691931	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime, downstream-variant-500B	NFX1, LOC105376018	GRCh38.p7	9:33348308	AGTGAGCCAATATCG[C/T]ACCACTGCACTCCAG	4799
rs149728466	snp	C/G	0.00874735	0.0655527	intron-variant	NFX1	GRCh38.p7	9:33307024	AGTGAAACTTTTTAT[C/G]AATAGCATTATATTT	4799
rs149806027	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33299247	CCAGTTTTTCTGCCA[A/G]TGTCCTTTTTCTGTT	4799
rs149865646	snp	A/G/T	4.94379e-05	0.00497161	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33351622	ACCCTGCAGTGCCAC[A/G/T]CTACCATGTGGGATG	4799
rs149939176	snp	C/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33344843	TGCACTCCAGCCTGG[C/T]GACAGACCAAGACTC	4799
rs149972499	snp	C/T	0.00478085	0.0486577	intron-variant	NFX1	GRCh38.p7	9:33362539	CACCACACGATCTCA[C/T]TCATATGTAGAATAT	4799
rs149999535	snp	C/T	0.00398564	0.0444627	intron-variant	NFX1	GRCh38.p7	9:33302440	GATCATGTCTCACTG[C/T]AGCCTTGAATTCCTG	4799
rs150027958	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33332876	TTTGAGACGGAGTCT[C/G]GCTCTGTTTCGCAGG	4799
rs150061598	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33320385	AGTTACTGTATTACA[C/T]TGAATGCAGTGGTGC	4799
rs150094037	snp	A/G	0.00199481	0.0315187	intron-variant	NFX1	GRCh38.p7	9:33341793	AAATTAGCCAGTTTC[A/G]TAACCCGGTCTCTAA	4799
rs150124256	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33300994	TACAAGGGGCATTTG[A/G]CTACTCTGCTGTTTT	4799
rs150128615	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33366944	AAGGCCTGAGCCAAA[A/G]AGCAAAACCTATGCC	4799
rs150163214	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33354566	TGAGGCCACTGGAGG[A/G]CTCCTAGACCCCATA	4799
rs150176337	snp	C/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33293777	TGGGATTGTAGACCA[C/G]ATTATAGAGGTTATG	4799
rs150183693	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33329373	TCTCTCCCGAGGTGT[A/G]CCGATACCATGTGAC	4799
rs150304652	snp	C/T	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33304370	TGGTAGAGTGATAGC[C/T]CTTGACACCTTTGAC	4799
rs150330215	snp	C/T	3.29598e-05	0.00405941	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33294546	GAAATTACAGTTCAC[C/T]ACCTCCCTGTCACCT	4799
rs150339610	snp	A/G	0.0170251	0.090679	intron-variant	NFX1	GRCh38.p7	9:33333920	GAGGCCAAGGTGGGC[A/G]GATCACCTGAGGTCA	4799
rs150373612	snp	A/G	0.00517822	0.0506191	intron-variant	NFX1	GRCh38.p7	9:33323344	AATGTCTAGTTTCCA[A/G]GAAAAAGTATGAAAT	4799
rs150408873	in-del	-/CA			intron-variant	NFX1	GRCh38.p7	9:33342129	TCTGTCTCTCTCTCT[-/CA]ACACACACACACACA	4799
rs150428184	snp	A/G	0.00199481	0.0315187	intron-variant	NFX1	GRCh38.p7	9:33324681	GCCTGTAATCCCAGC[A/G]TTTTGGGAGGCTGAG	4799
rs150565627	snp	C/G	0.00119737	0.0244387	intron-variant, utr-variant-3-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33347808	CAACAAGTGGATAAA[C/G]AAATTGTGGTGTATC	4799
rs150653467	snp	A/G	0.00676609	0.0577691	intron-variant	NFX1	GRCh38.p7	9:33338108	ACCTGTAATCTCAGC[A/G]CTTTGGGAGGCCATG	4799
rs150654226	snp	A/G	0.00199481	0.0315187	intron-variant	NFX1	GRCh38.p7	9:33334657	TTTCCCTAGATTTAG[A/G]CTTATACTAAAGATA	4799
rs150670270	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB	NFX1	GRCh38.p7	9:33290351	TCCCTCCTGCGATTG[C/T]TGCTATTTCCATCCA	4799
rs150741551	snp	A/G	0.00993419	0.0697739	intron-variant	NFX1	GRCh38.p7	9:33326583	AAATTACCCAGACAT[A/G]GTGGTATGTGCCTGT	4799
rs150757609	in-del	-/T			intron-variant	NFX1	GRCh38.p7	9:33335228	TATCTTTCTTTTTCT[-/T]TTTTTTTTTTTTTTT	4799
rs150758345	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33364625	CATTGTCTATTGTCT[A/G]CGCTTTACAGGGAGA	4799
rs150805516	snp	G/T	1.64779e-05	0.00287031	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33318996	TCCCCCAGCTGGTGC[G/T]CTGTTGCCCCTGTGG	4799
rs150828550	snp	C/T	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33343966	CCCCATAAATTCTCC[C/T]CTAAAAATACAAGCA	4799
rs150843879	snp	A/G	0.000428294	0.0146275	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33295290	CCTGTGACAGTGAGA[A/G]CTTGGCAGTCATCAA	4799
rs150864129	snp	A/C	0.00199481	0.0315187	intron-variant	NFX1	GRCh38.p7	9:33302171	ATATTTTGATACAAG[A/C]GTACAATGTGTAATG	4799
rs150916896	snp	A/G	0.0221141	0.102801	intron-variant	NFX1	GRCh38.p7	9:33296786	TCACCTTTATAGATA[A/G]CGTTAATCTCTTACA	4799
rs150917219	snp	C/T	0.200801	0.245111	intron-variant	NFX1	GRCh38.p7	9:33369214	GGGACTACAGGCGCC[C/T]GCCACCACGCCCGGC	4799
rs150967666	snp	G/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33341195	TTACAGTTCCAAGTG[G/T]CTGGGGAGGCCTCAC	4799
rs150989553	snp	A/C	0.00716266	0.059414	intron-variant	NFX1	GRCh38.p7	9:33293269	AGTTAATACATGTAA[A/C]GTGCTTAGGATAGTG	4799
rs151057046	snp	A/G	0.0134861	0.0810011	intron-variant	NFX1	GRCh38.p7	9:33329084	GCTTTACTACAAGGA[A/G]GTTACAGTTTTATTA	4799
rs151063667	snp	A/C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33343930	TAATAAAATAAAAAC[A/C/T]TCTTTTGAAAAAAGT	4799
rs151073937	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33366475	TCTTCCCAAACCCCT[C/T]CAGGCTTGCTTGGCA	4799
rs151110941	snp	A/G	0.00318978	0.0398085	intron-variant	NFX1	GRCh38.p7	9:33323943	AAAAGTAGGATAACC[A/G]AAATGCAAAATTCAT	4799
rs151146557	snp	C/T	0.0134861	0.0810011	intron-variant	NFX1	GRCh38.p7	9:33319666	AGGCGCACACCACCA[C/T]GCCCGGCTAATTTTT	4799
rs151183891	snp	A/G	0.00199481	0.0315187	intron-variant	NFX1	GRCh38.p7	9:33300345	TGGTATTACAGGTGT[A/G]AGCCACCGTGTCCAA	4799
rs151267155	snp	A/G	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33362470	TTTGCAACAACATGG[A/G]TGGACCTGGAGGACA	4799
rs151267247	snp	G/T			intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352207	AACTAATTATGGCTG[G/T]GGTGTCATGAGGGAG	4799
rs151316654	snp	A/G	3.29625e-05	0.00405958	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33347079	AAGTGTCCCCCTTGC[A/G]CTTTCCTAACTCAGA	4799
rs151319816	snp	A/G	0.0023933	0.0345097	intron-variant	NFX1	GRCh38.p7	9:33356272	ACTGGCCATTGGATA[A/G]CCTCATTTTTGAAGT	4799
rs180741260	snp	A/T			intron-variant	NFX1	GRCh38.p7	9:33312410	TAGTGTTAGCCATTA[A/T]GTCAAGTACTGCAAG	4799
rs180753204	snp	A/C	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33337278	AAATTTTTTCTCATC[A/C]TTTTCTAATAGCATT	4799
rs180753966	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33301847	GAGGCCAAGGCAGGC[A/G]GATCATCTGAAGTCA	4799
rs180764161	snp	A/G	0.00279162	0.0372561	intron-variant	NFX1	GRCh38.p7	9:33326934	ATAAATCTGAAGTAG[A/G]TTCTGATAAGATGTA	4799
rs180765120	snp	C/T	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33358193	GCAATGGTGTGATCT[C/T]GGCTCACTGCAAGCT	4799
rs180961227	snp	C/T	0.000798403	0.0199641	intron-variant, utr-variant-3-prime, downstream-variant-500B	NFX1, LOC105376018	GRCh38.p7	9:33348469	CATGTAACCAAACAC[C/T]ACCTGTTCCCCAAGA	4799
rs180978869	snp	C/T	0.00199481	0.0315187	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33365906	CCCCTGTCCTGGAGG[C/T]GGCCAGGGATGTCAC	4799
rs181210602	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33331783	TGGCAACCTGTAAAT[G/T]ACATCAAAGCCAAAA	4799
rs181211311	snp	A/C	0.00398564	0.0444627	intron-variant	NFX1	GRCh38.p7	9:33306795	TCTTACTGCCTCCCC[A/C]CTTTCCCCACGGTGC	4799
rs181229314	snp	C/T	0.00517822	0.0506191	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33353377	TGGGACCTGTGTAGC[C/T]GTACAGGGATCTGAG	4799
rs181250490	snp	G/T	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33369734	GAAGGAAACACAAAA[G/T]TTAAAAAAATTGCTC	4799
rs181296359	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33325774	CTAGCAGGCAGACTT[A/G]CCTTACAGTAAGTAC	4799
rs181311047	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33365278	AAACTCTGTCTCAAA[A/G]AGAAAGAAAGAAAGA	4799
rs181315369	snp	G/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33362248	ATAGAACTACCATAT[G/T]ATCCAGCAATCCTAT	4799
rs181372734	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33300696	TCACTGGACTTTGAG[C/T]TCCTGGAGCCAGGGA	4799
rs181389399	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33347858	TACTCAGCCAGGAAC[A/G]AAATAATGGCATTCA	4799
rs181432918	snp	A/C	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33321022	GGTTCTCTGCTTGCC[A/C]TGAAAATGTGTTTAT	4799
rs181441879	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33342088	ACCACCACACTCCAG[C/T]CTGGGCAACAGAGTG	4799
rs181514684	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33306473	GATCAATGGCCTTTA[A/G]GTGGATTGCACCTCT	4799
rs181533318	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352877	CCACTGCACAGATAC[A/T]TGTGTTTATCATAGT	4799
rs181664348	snp	G/T	0.00358779	0.0422022	intron-variant	NFX1	GRCh38.p7	9:33293653	ATTTTATGTCCTTAG[G/T]CAAACCATTTTGTCT	4799
rs181670291	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33330318	CATCTGACTTGCGAA[C/T]AATTCTGAGGATATA	4799
rs181761997	snp	A/C			intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33350911	AGCACTTTGGGAGGC[A/C]AAGGCAAGTGGATCA	4799
rs181835958	snp	C/T	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33347260	AATTTTTTCTTAAGA[C/T]ATAATTTGCATACAA	4799
rs181836176	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33364601	TGATCTCTGCAGTTT[C/T]ACTGCCAGCATTGTC	4799
rs181844428	snp	A/T	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33313516	TTGGAGGAGGGAGAC[A/T]TAGGAAAAAGTGAGG	4799
rs181845942	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33338006	GTGAGCCAAGATTGC[A/G]CCATTGCACTCCAGC	4799
rs181884877	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33341747	CCAGCCTTGGCAACA[C/T]GGTAAAACCCCATCT	4799
rs181886509	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33320637	TACTATACTGAGCCT[A/G]TCTGACTCAGTCTTT	4799
rs181957283	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	NFX1	GRCh38.p7	9:33370453	TTTTTTAGTCTGAAA[C/T]ACCAAATAATGAATT	4799
rs182028442	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33299108	TTCAAAGAATTCCCA[C/T]ATATCTTTCACCCAA	4799
rs182032670	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33292514	ACTTGTATTCTAGCC[A/G]TGGTGACTAGACATC	4799
rs182150320	snp	C/T	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33361769	CAAGAGCAGCCTGGG[C/T]GACAAGAGCAAGACT	4799
rs182153488	snp	G/T	0.0023933	0.0345097	intron-variant	NFX1	GRCh38.p7	9:33332129	TTTCTGTCTGTACCC[G/T]TGTTTGGTGATGACT	4799
rs182315289	snp	C/T	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33325112	AATAATAGATAAAAA[C/T]TTTCAAATGTATTGA	4799
rs182369870	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33359276	TGGTTAGGGCCTTCA[C/G]TATATTGTTGAATGG	4799
rs182409540	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33307666	TCATATGTTTTATCC[C/T]GCATTGATATCCAGG	4799
rs182424215	snp	C/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33354538	TTTGGGGCTGAGCAG[C/G]CAGGGAACACTCTGA	4799
rs182514494	snp	A/G	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33309154	CGAGGCCAGGAGATC[A/G]AGACCATCCTGGCTA	4799
rs182520583	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33333753	AAAGAGAAGAGTGGC[C/T]GTTTGGGAGGTACCC	4799
rs182527068	snp	A/T	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33355485	TCTTTCGTTATATTT[A/T]TGTGACATTCACTCC	4799
rs182559248	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33314973	TACATGAATAGAAAA[A/G]AATTTTTTAATTGTG	4799
rs182561834	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33304044	GGCCAAGGTAGGTGG[A/G]TCACCTGAGATCAGG	4799
rs182562309	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33339412	CTTATTCACTATCAC[A/G]AGAACAGCACAAGAA	4799
rs182567295	snp	A/G	0.02016	0.0983543	intron-variant	NFX1	GRCh38.p7	9:33359370	TTGGGAGACTGAGGC[A/G]GGCGGATCACTTGAG	4799
rs182674479	snp	G/T	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33316385	TCAGCCTCCCAAGTA[G/T]CTGGCACTACAGATG	4799
rs182696961	snp	A/G	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33359937	TGAAGTTTGACTTTC[A/G]GCAATTTTAATAGTA	4799
rs182788136	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33308421	CACTCCAGCCTGGGC[A/G]ACAAAGCAAGACCAT	4799
rs182955606	snp	A/C			upstream-variant-2KB	NFX1	GRCh38.p7	9:33289898	CACCCCTCCCTGGGC[A/C]CCCAAGTGAGATTGC	4799
rs182960024	snp	C/T	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33296090	CGCCACCATGCTTGG[C/T]TGATTTTTGTATTTT	4799
rs182967265	snp	C/T	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33343866	ATAAATGAAACTTCA[C/T]ATCTGTTCATGCCTT	4799
rs182971085	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33339628	CATTTCAGCATTAAC[A/G]CAAAAGTCTACAGTC	4799
rs183019930	snp	C/T			upstream-variant-2KB	NFX1	GRCh38.p7	9:33288592	TTCCATTGTTAGCAG[C/T]TGTTTGCAGAATTTT	4799
rs183067366	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33328278	GATCCTCCCACCTCA[C/G]CCTCTCAAAGTGCTG	4799
rs183075040	snp	A/G	0.00279162	0.0372561	intron-variant	NFX1	GRCh38.p7	9:33367766	GTAATGTTTAGTTAG[A/G]GTATCAGACACGTTT	4799
rs183152829	snp	C/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33345110	GAGGTTGCAGTGAGC[C/T]AAGATTGTGCCACTG	4799
rs183218075	snp	A/G	0.00159617	0.0282053	intron-variant	NFX1	GRCh38.p7	9:33360968	AATAACTTGAATGTT[A/G]GTGAGATGCCATGAG	4799
rs183250189	snp	A/C	0.00199481	0.0315187	intron-variant	NFX1	GRCh38.p7	9:33321870	GCTGACAGAGTGAGA[A/C]CCTGTCTCAAAAAAA	4799
rs183337743	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33350245	GGAGGTGGAGGTTGC[A/G]GTGAGCTGAGATGGC	4799
rs183350451	snp	C/G	0.00438332	0.0466095	upstream-variant-2KB	NFX1	GRCh38.p7	9:33290405	CGACACCTGGCGCGT[C/G]TATCTGACGTCACGA	4799
rs183359351	snp	A/G			intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33366545	CTCTTATTGATCCCT[A/G]CAATTCTTGTGTGGT	4799
rs183364583	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33339726	TACTTCCTAGGTCCA[A/G]TGGGAGTACAGGCAT	4799
rs183367103	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33317705	TTATGGCCGGGCGTG[A/G]TGGCTCACGCCTGTA	4799
rs183395982	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33296925	CCTTAAAAACAGACA[C/G]TGTATATTTCTTTTC	4799
rs183414160	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33322651	GGCAGAGGTTCCACT[A/G]AGAGAAGCAAGCCAA	4799
rs183440353	snp	A/G	0.00914312	0.0669923	intron-variant	NFX1	GRCh38.p7	9:33362670	TAAAGTTACAAATAG[A/G]TGGTAGTAATAAGTT	4799
rs183544766	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33364441	TCTCACATTCACATG[C/T]GTTCTCAGTTGGAGC	4799
rs183556658	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33355005	CGCTGCGTCTTTTAC[C/T]GTTATCAAAGAGCAA	4799
rs183558649	snp	A/T	0.00279162	0.0372561	intron-variant	NFX1	GRCh38.p7	9:33323499	GTGGCTCACGCCTGT[A/T]ATCCCAGCACTTTGG	4799
rs183737793	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33329312	TTATTGGTGCTCTAT[C/T]GTGCAATCATAGTTG	4799
rs183739482	snp	C/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33304944	AAATTAGATGAGAGA[C/T]TCTAAGGCAGTATAA	4799
rs183753050	snp	A/G	0.00438332	0.0466095	intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33351037	TAACCCCAGCTACTC[A/G]GGAGGCTGAGGCTGG	4799
rs183757919	snp	A/C	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33368473	CTGAGAGTTGGGTGA[A/C]TGTTGGGCTTTATTT	4799
rs183779009	snp	G/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33333070	AGGCTGGTCTCTAAC[G/T]CCTGACCTCAAGTGA	4799
rs183783991	snp	C/G	0.0023933	0.0345097	intron-variant	NFX1	GRCh38.p7	9:33297302	GAAGCCACCATCTAC[C/G]CAGGGCCTGTTTTTA	4799
rs183795003	snp	G/T	0.000399281	0.0141238	downstream-variant-500B	NFX1	GRCh38.p7	9:33371274	CTGCTTCAAAAGGGA[G/T]CAGGTACAGCAGCAG	4799
rs183841570	snp	C/T	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33303487	ACCAGGCTCATGCTG[C/T]TTCTGGGCTGTAGTG	4799
rs183850453	snp	A/G	0.00755907	0.0610114	intron-variant	NFX1, LOC105376018	GRCh38.p7	9:33349653	CTATGGTGAGGAAGC[A/G]TGGAAACAGGCCATT	4799
rs183948386	snp	A/T	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33335135	CCATTTTAAATGTAC[A/T]GTTCAGTGGCACTTA	4799
rs183992350	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33311963	AGTATCTGGCATCTA[A/G]GAGTCTTTTAATGAA	4799
rs183999309	snp	A/G			intron-variant	NFX1	GRCh38.p7	9:33337111	CAAATTCCTGGGCTC[A/G]AGCAATCCTCCTGCC	4799
rs184000911	snp	C/T	0.00279162	0.0372561	intron-variant	NFX1	GRCh38.p7	9:33357676	AGATAGGACTACAGG[C/T]ACACACCACTACGCC	4799
rs184030847	snp	A/C	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33327217	TTTTATAGAGGTGGA[A/C]TCTCACTCTATTTCC	4799
rs184123192	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33356168	TTTTTAATTTTAGCC[A/G]TTTTGTAGATGTGTA	4799
rs184252154	snp	C/T	0.00318978	0.0398085	intron-variant	NFX1	GRCh38.p7	9:33306547	GCAGAGGCCATGGAC[C/T]GGGGATGGCTGCAAT	4799
rs184258546	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33330358	TGGGAAGCTAGTTTA[A/G]TAGGAAAACTTCAGA	4799
rs184261438	snp	C/T	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33361224	TATGAGCCATGAAGA[C/T]AGTTAAGTGTGAAAA	4799
rs184490310	snp	C/T	0.000798403	0.0199641	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33365142	AGCTGGGTGTGGTGG[C/T]GGGCACCTGTTATTC	4799
rs184515498	snp	G/T	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33361441	CTTATTTTTGGGGGG[G/T]TGAGACAATTTTGAA	4799
rs184556016	snp	A/G	0.00199481	0.0315187	intron-variant	NFX1	GRCh38.p7	9:33346159	TTGCAAGCCCCTCCT[A/G]TGGCATTCATACCAG	4799
rs184558451	snp	A/G	0.00199481	0.0315187	intron-variant	NFX1	GRCh38.p7	9:33361818	ATATATACACATAGA[A/G]AGAAACGTTATAGTG	4799
rs184631338	snp	A/C			intron-variant	NFX1	GRCh38.p7	9:33292206	AGTATCTAATGAGGC[A/C]AAATCTTCTAGTCCA	4799
rs184642613	snp	A/G	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33341437	AGATAAGATTTGGGT[A/G]GAGACACAGCCAAAC	4799
rs184672898	snp	C/T	1.64795e-05	0.00287045	intron-variant	NFX1	GRCh38.p7	9:33311193	GTAAAGTTAAAATTA[C/T]ACCCTAAAGAAGACC	4799
rs184690473	snp	C/T			intron-variant	NFX1	GRCh38.p7	9:33324494	AGGTTGAGGTTGCAG[C/T]AAGCCATGATCATGC	4799
rs184707596	snp	C/T	0.00234993	0.0341971	intron-variant	NFX1	GRCh38.p7	9:33364000	TTGCATACCTCTCTC[C/T]CTCTTTCAGGAGATT	4799
rs184751999	snp	A/C	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33298033	ATATTTGTTGCATAA[A/C]TACTATATACCAAGC	4799
rs184763542	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33298810	TATTATTAAGCTGCT[A/G]TGTGGAGAATAGGCT	4799
rs184768985	snp	A/C/T	0.261884	0.249717	intron-variant	NFX1	GRCh38.p7	9:33324928	AGTGAGATTCCATCT[A/C/T]AAAAAAAAAAAAAAA	4799
rs184831289	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33290820	TTCGGAGGAGAGAGG[A/G]CTTGTCCCGGCGCTG	4799
rs184948964	snp	A/G/T	0.000362408	0.0134566	missense, nc-transcript-variant	NFX1	GRCh38.p7	9:33318924	GGGACTTGAAATGCG[A/G/T]TAACCATACATGTTC	4799
rs185080709	snp	A/G	0.00318978	0.0398085	intron-variant	NFX1	GRCh38.p7	9:33369353	CAGGCGTGAGCCACC[A/G]CACCTGGCCATCCCA	4799
rs185186809	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	NFX1, LOC105376018	GRCh38.p7	9:33352951	TTTTGTTTTGTTTTA[C/T]TGAGAGGGGTCTCGC	4799
rs185230560	snp	A/G	0.000798403	0.0199641	intron-variant	NFX1	GRCh38.p7	9:33327040	CTATAAAAAATATTG[A/G]CAAAATGCAAATGAA	4799
rs185237011	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33302169	TGATATTTTGATACA[A/G]GCGTACAATGTGTAA	4799
rs185241692	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B, nc-transcript-variant	NFX1, LOC105376018	GRCh38.p7	9:33348844	CTTGCTGTGGTTAAG[A/G]TGATACTGTTTGCTA	4799
rs185257472	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	NFX1	GRCh38.p7	9:33366001	CTCCCCCTTCCATCA[A/G]GGGGGACGGTGAGTA	4799
rs185319858	snp	C/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33356915	GAAGATTGCTTGAAC[C/G]TGCGAGGTTGAGGCT	4799
rs185333880	snp	A/C	0.00119737	0.0244387	intron-variant	NFX1	GRCh38.p7	9:33339422	ATCACGAGAACAGCA[A/C]AAGAAAGACCTGCCC	4799
rs185336336	snp	A/G	0.000399281	0.0141238	intron-variant	NFX1	GRCh38.p7	9:33325314	CTCATCAGAAACAAT[A/G]GAGAACACATCACAA	4799

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