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

NSMAF

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs901954	snp	A/T	0.494896	0.0502606	intron-variant	NSMAF	GRCh38.p7	8:58613180	ttaaaaatactaaaa[A/T]atatttttaatactt	8439
rs931396	snp	A/T	0	0	intron-variant	NSMAF	GRCh38.p7	8:58587448	TTAGGTTTCCAAGTC[A/T]ACTTTGTTTTGTTTT	8439
rs973807	snp	C/T	0.499713	0.0119774	intron-variant	NSMAF	GRCh38.p7	8:58658728	TGTCACCAAAAATGC[C/T]CTGGGAACTATACAT	8439
rs1050488	snp	C/T	0.393987	0.204372	utr-variant-3-prime	NSMAF	GRCh38.p7	8:58583931	AAAGCCATTAGTTGC[C/T]ATTCTCTTAGGGCAG	8439
rs1050504	snp	A/G	0.3744	0.216852	utr-variant-3-prime	NSMAF	GRCh38.p7	8:58583857	CAGATGATCGTCCCC[A/G]TATGATGATTGTCAG	8439
rs1352496	snp	C/G	0.368119	0.220336	intron-variant	NSMAF	GRCh38.p7	8:58636433	GTACCCGTGTACTAC[C/G]TCTGAAAGTATTCTT	8439
rs1387222	snp	A/T	0.435407	0.167703	intron-variant	NSMAF	GRCh38.p7	8:58643172	TGTTTGTTAAATTCA[A/T]GAATGGAAAAGCTTT	8439
rs2054900	snp	A/G	0.147991	0.228242	intron-variant	NSMAF	GRCh38.p7	8:58601976	TTCCCCTAAGCCTTG[A/G]AGAAACGAATTTCCT	8439
rs2130072	snp	C/T	0.372592	0.217879	intron-variant	NSMAF	GRCh38.p7	8:58614140	tcacaacatatgagg[C/T]gggaaattaaagaaa	8439
rs2228505	snp	A/G/T	0.0621084	0.164914	missense	NSMAF	GRCh38.p7	8:58595575	AGTTACACGAGCACT[A/G/T]TAAAATCCACAAAGA	8439
rs2228506	snp	A/G/T	0.000164786	0.00907584	synonymous-codon	NSMAF	GRCh38.p7	8:58597514	GGTAGCCATGCTTAC[A/G/T]CAAATCTTGGAATTT	8439
rs2229740	snp	A/G/T	0.00694917	0.0585432	synonymous-codon	NSMAF	GRCh38.p7	8:58589470	GCTATATTCTGCATC[A/G/T]TGGGACTCTACAGTG	8439
rs2242344	snp	G/T	0.486595	0.0807641	intron-variant	NSMAF	GRCh38.p7	8:58658989	GAATCAGGCCTTTCC[G/T]GCGGCCCCCCTCCCA	8439
rs2255834	snp	A/G	0.496783	0.0399767	intron-variant	NSMAF	GRCh38.p7	8:58603197	TGGTCAGAATTCCAC[A/G]TGTGGCAGTTACCTA	8439
rs2279459	snp	C/G	0.152001	0.229992	intron-variant	NSMAF	GRCh38.p7	8:58595874	AAGTATAAAAAGATT[C/G]TAGTATTATTCAAAG	8439
rs2279460	snp	A/G	0.491783	0.0635686	intron-variant	NSMAF	GRCh38.p7	8:58595816	TTTTCCTTGACTAAC[A/G]TGGAACCATCTAACA	8439
rs2279462	snp	G/T	0.491421	0.0649309	intron-variant	NSMAF	GRCh38.p7	8:58595391	ATCTCCACCTGAGGT[G/T]GATGTAGTAGGGAAA	8439
rs2326129	snp	C/T	0.499539	0.0151687	intron-variant	NSMAF	GRCh38.p7	8:58611978	TCTCTGCTCCCAGTT[C/T]GTGGCACAGAGCTCC	8439
rs2634488	snp	C/T	0.499999	0.000798721	intron-variant	NSMAF	GRCh38.p7	8:58598751	ACAGGTGTGAGCCAC[C/T]GCGCCCAGCCCCTGG	8439
rs2634489	snp	C/T	0.5	0	intron-variant	NSMAF	GRCh38.p7	8:58598498	tcttttttttttttt[C/T]tttttttgtttgaga	8439
rs2634527	snp	A/G	0.483995	0.0880135	intron-variant	NSMAF	GRCh38.p7	8:58586830	CTTTAGCAATACTTC[A/G]TTTCTTCTTGTATTC	8439
rs2634529	snp	A/G	0.188946	0.24243	intron-variant	NSMAF	GRCh38.p7	8:58602953	TAATGATAACCCTGG[A/G]TTAAAATCATGCCCA	8439
rs2634530	snp	A/C	0.495135	0.0490805	intron-variant	NSMAF	GRCh38.p7	8:58603597	AAATTATTAAATACA[A/C]TGAGCTATTACACTA	8439
rs2634531	snp	C/T	0.497586	0.0346604	intron-variant	NSMAF	GRCh38.p7	8:58604499	AGCTTAATGTATGAA[C/T]AAAATACTAGCTATA	8439
rs2634532	snp	A/G	0.121717	0.214577	intron-variant	NSMAF	GRCh38.p7	8:58606960	AGCTCTATACCCAAA[A/G]GAGGAGATTTTTAAT	8439
rs2634533	snp	C/G	0.118933	0.212888	intron-variant	NSMAF	GRCh38.p7	8:58623063	AGGAGAACTCTCTAG[C/G]GCTTCCTCAACTCTT	8439
rs2634534	snp	C/T	0.494484	0.0522255	intron-variant	NSMAF	GRCh38.p7	8:58614479	AGGTTATAGGATAAG[C/T]CTGTGCCTAGGCAAA	8439
rs2680896	snp	A/G	0.16618	0.23553	intron-variant	NSMAF	GRCh38.p7	8:58603922	AAGAAGAAAACAGGC[A/G]TTTGGCAGGAGGACC	8439
rs2680897	snp	A/G	0.494143	0.0537956	intron-variant	NSMAF	GRCh38.p7	8:58607078	CAAATTAAAAGCACA[A/G]AAATAAGAATTAAAA	8439
rs2680898	snp	A/G	0.121717	0.214577	intron-variant	NSMAF	GRCh38.p7	8:58607232	AGTAAGACATGTGTC[A/G]GAAATAGGACCTAAG	8439
rs2680899	snp	C/T	0.494774	0.0508504	intron-variant	NSMAF	GRCh38.p7	8:58609475	ATACACAGATGCTGC[C/T]TGTGAAGGGGGTGGG	8439
rs2680900	snp	A/G	0.122064	0.214785	intron-variant	NSMAF	GRCh38.p7	8:58609976	AGCCATGACAGACAA[A/G]TAAATAATACCAAAT	8439
rs2680901	snp	C/T	0.49533	0.0480965	intron-variant	NSMAF	GRCh38.p7	8:58610885	CTGTGGAAGAGAAAG[C/T]CTTTATCACTCCCTC	8439
rs2680903	snp	C/T	0.128684	0.218592	synonymous-codon	NSMAF	GRCh38.p7	8:58599775	ACAGATGGTTGACGA[C/T]GTGGAGCTTCCCCCT	8439
rs2680904	snp	C/T	0.162253	0.234095	intron-variant	NSMAF	GRCh38.p7	8:58598687	CTTTTGCCCAAATAA[C/T]ACCAAATTCATCCTG	8439
rs2946577	snp	C/T			intron-variant	NSMAF	GRCh38.p7	8:58600619	agagcaagactttgt[C/T]tcaaaaaaaaaaaaa	8439
rs2946578	snp	C/T	0.493837	0.055168	intron-variant	NSMAF	GRCh38.p7	8:58602515	GTGAATATTATTATT[C/T]TTCAATATTAGCCTA	8439
rs2969915	snp	A/T	0.147991	0.228242	intron-variant	NSMAF	GRCh38.p7	8:58602569	CTAGAAATATGATAA[A/T]GTATTTCTCTGAAAA	8439
rs2969916	snp	A/G			intron-variant	NSMAF	GRCh38.p7	8:58600615	tttttttttgagaca[A/G]agtcttgctctgtcg	8439
rs3736236	snp	C/T	0.046008	0.144524	intron-variant	NSMAF	GRCh38.p7	8:58589976	CCCTGCTCTGTGATT[C/T]GACGTGCAGAATAGC	8439
rs3739327	snp	A/G	0.498034	0.0312882	downstream-variant-500B	NSMAF	GRCh38.p7	8:58583493	AGTTACTTAAATAAA[A/G]TGAAAACAGCTTTCT	8439
rs3816846	snp	C/T	0.381891	0.212379	intron-variant	NSMAF	GRCh38.p7	8:58586678	GACTACATATTTGAA[C/T]CAGACTAGAGAAACA	8439
rs3816847	snp	A/G	0.186737	0.241863	intron-variant	NSMAF	GRCh38.p7	8:58603551	AGTATTTGTTCAGCT[A/G]TGTATAAACAGTTCC	8439
rs3837194	in-del	-/T	0.498392	0.028309	downstream-variant-500B	SDCBP, NSMAF	GRCh38.p7	8:58583149	AATATTTAATAACAC[-/T]TGAAACTGACTTTGG	8439
rs4266636	snp	A/G	0.419936	0.183362	intron-variant	NSMAF	GRCh38.p7	8:58619986	AAGGTATAATAATTA[A/G]CTTAGTGGTACCAGA	8439
rs4421339	snp	A/G	0.0901694	0.192235	intron-variant	NSMAF	GRCh38.p7	8:58630098	CAATCATGTGGTGCT[A/G]TGTGGGACAGAGGAT	8439
rs4598239	snp	G/T	0.411746	0.190626	intron-variant	NSMAF	GRCh38.p7	8:58620148	AAACCATTAGAACAG[G/T]AGAAGTGTACTCTCT	8439
rs4737504	snp	A/G	0.493969	0.05458	intron-variant	NSMAF	GRCh38.p7	8:58628020	ccaaaatagcatggg[A/G]ctagtataacaacag	8439
rs4737505	snp	A/G	0.214843	0.247516	intron-variant	NSMAF	GRCh38.p7	8:58644964	CGGGGACCTGTTGGC[A/G]GGGTGGGGAGCTAGA	8439
rs4738695	snp	C/G	0.183886	0.241099	intron-variant	NSMAF	GRCh38.p7	8:58609412	AACAGATCAGAAGAA[C/G]TCAAACTTCAGAGAC	8439
rs4738696	snp	C/T	0.305436	0.243776	intron-variant	NSMAF	GRCh38.p7	8:58611577	GTTTCAGCAGAGAAA[C/T]AGAAACTATGAAAAA	8439
rs4738697	snp	C/T	0.0349115	0.127424	intron-variant	NSMAF	GRCh38.p7	8:58620467	CCATGTTAAGGTGTT[C/T]AGGCTTTATCCTGAA	8439
rs4738699	snp	C/T	0.490287	0.0690083	intron-variant	NSMAF	GRCh38.p7	8:58654830	ATCTAAATTTCTTTT[C/T]TATTATGTATTTATT	8439
rs5891688	in-del	-/TGAT	0.383053	0.211653	downstream-variant-500B	SDCBP, NSMAF	GRCh38.p7	8:58583103	ACTCATTGAGGCTAC[-/TGAT]TGATTGTCCCTAGCA	8439
rs5891689	in-del	-/ATTG			downstream-variant-500B	SDCBP, NSMAF	GRCh38.p7	8:58583109	TGAGGCTACTGATTG[-/ATTG]TCCCTAGCAATACCT	8439
rs5891691	in-del	-/A	0.365024	0.221967	upstream-variant-2KB	NSMAF	GRCh38.p7	8:58660100	GTGTCCTCCATTGTG[-/A]AAAAAAAAAAAAGAC	8439
rs6471732	snp	C/T	0.419296	0.183954	intron-variant	NSMAF	GRCh38.p7	8:58626583	attccatggtgtata[C/T]atataggactttttc	8439
rs6985007	snp	G/T	0.499954	0.00479211	intron-variant	NSMAF	GRCh38.p7	8:58649186	tcataggagattatt[G/T]tggagttttaagatt	8439
rs6985643	snp	A/G	0.499839	0.00898417	intron-variant	NSMAF	GRCh38.p7	8:58649528	atgtttgtcccctcc[A/G]aatctcatgttaata	8439
rs6991020	snp	A/G	0.497959	0.0318836	intron-variant	NSMAF	GRCh38.p7	8:58592819	TTGAACCCAGGAGGC[A/G]GAGGTTGCAGTGAGC	8439
rs6991479	snp	C/T	0.305186	0.243833	intron-variant	NSMAF	GRCh38.p7	8:58610191	AATACATTTGAGTAA[C/T]TGTATATTCCTTTGT	8439
rs6991644	snp	A/G	0.307671	0.243257	intron-variant	NSMAF	GRCh38.p7	8:58610347	GAAAAAATAAGGGAA[A/G]ACAACCAAATCATCA	8439
rs6994461	snp	C/T	0.17332	0.23795	intron-variant	NSMAF	GRCh38.p7	8:58654609	AATATTATACACTCA[C/T]GGAATGTCTGAAACA	8439
rs6994565	snp	C/T	0.130351	0.219509	intron-variant	NSMAF	GRCh38.p7	8:58598854	atggtgaaaccgtca[C/T]gaccaaaaaaaatac	8439
rs6994622	snp	C/G/T	0.0209503	0.100241	intron-variant	NSMAF	GRCh38.p7	8:58656488	ataaaaatatcatat[C/G/T]cccagttacatttga	8439
rs6995115	snp	A/G	0.498369	0.0285077	intron-variant	NSMAF	GRCh38.p7	8:58586055	CAGAATGTGGTTTAC[A/G]TTATTCTGGATTTTA	8439
rs6998210	snp	C/T	0.418007	0.185132	intron-variant	NSMAF	GRCh38.p7	8:58625691	ccgaaaatgagtctc[C/T]tgcagatggcatata	8439
rs7001188	snp	C/T	0.111224	0.207945	intron-variant	NSMAF	GRCh38.p7	8:58645004	gcattaggagaaata[C/T]ctaatgtagatgatg	8439
rs7006797	snp	A/G	0.496999	0.0386216	intron-variant	NSMAF	GRCh38.p7	8:58588588	AAGCAAATAGGCATC[A/G]AAGATGCTCGCTTCA	8439
rs7006937	snp	C/G	0.414905	0.187899	intron-variant	NSMAF	GRCh38.p7	8:58618624	taacacacacacaca[C/G]aGAGCAACAATGTGA	8439
rs7008292	snp	C/T	0.130351	0.219509	intron-variant	NSMAF	GRCh38.p7	8:58597156	GCCAACTTTCACTCA[C/T]ATTCAATTGCCAGAA	8439
rs7011033	snp	C/T	0.0325976	0.123435	intron-variant	NSMAF	GRCh38.p7	8:58618909	TTTCATTTCATATGG[C/T]AAAAATCCCTTCCCC	8439
rs7011066	snp	C/G	0.412082	0.190341	intron-variant	NSMAF	GRCh38.p7	8:58618972	ATACATTAAAACGTT[C/G]ACAGTGAACTATTTT	8439
rs7014666	snp	C/G	0	0	intron-variant	NSMAF	GRCh38.p7	8:58632073	CCTGTACTTTCCTCA[C/G]TGCTTTTCCTCCTGC	8439
rs7015319	snp	A/G	0.26326	0.249648	intron-variant	NSMAF	GRCh38.p7	8:58594912	CATGACCTGTATGCC[A/G]GAGGGGCTGTCTGTC	8439
rs7015870	snp	G/T	0.0952156	0.196321	intron-variant	NSMAF	GRCh38.p7	8:58625386	tatgtctgtatatat[G/T]tatatgcatatgtat	8439
rs7465261	snp	C/T			upstream-variant-2KB	NSMAF	GRCh38.p7	8:58660356	ggagggtgggggatt[C/T]ttgctaaactgccgt	8439
rs7816499	snp	C/T	0.305436	0.243776	intron-variant	NSMAF	GRCh38.p7	8:58612566	ctaaggaatgtgttg[C/T]gggaatctctgattt	8439
rs7820921	snp	A/C	0.493386	0.0571263	intron-variant	NSMAF	GRCh38.p7	8:58650097	AAGCACTTGGGTACC[A/C]TTTGCATCTTCACCC	8439
rs7825739	snp	C/T	0.418814	0.184396	intron-variant	NSMAF	GRCh38.p7	8:58606917	AAAGCACTTAATCAA[C/T]GTTAATTTCTTCTCT	8439
rs7826122	snp	A/G	0.499502	0.0157669	intron-variant	NSMAF	GRCh38.p7	8:58593570	CCCTTCCATCTCTGC[A/G]TCTTCCAGAGTGCCA	8439
rs7826603	snp	A/G	0.499527	0.0153681	intron-variant	NSMAF	GRCh38.p7	8:58593628	AAGACATACTTTAAT[A/G]AATAATATATAATGC	8439
rs7830228	snp	A/C	0.498611	0.0263212	intron-variant	NSMAF	GRCh38.p7	8:58657617	GATTCCAGTGCATAC[A/C]TGATGTGAGACAGAT	8439
rs7831185	snp	A/G	0.121717	0.214577	intron-variant	NSMAF	GRCh38.p7	8:58617494	acccatcaaaaagtg[A/G]gcaaaggatatgaac	8439
rs7833097	snp	A/G	0.110519	0.207473	intron-variant	NSMAF	GRCh38.p7	8:58635709	ATTAACTGGTAAAAC[A/G]AAACACAGAATAGTG	8439
rs7833791	snp	C/T	0.409382	0.192607	intron-variant	NSMAF	GRCh38.p7	8:58630142	cacaaatttttatac[C/T]ggctttgatgtggtt	8439
rs7836960	snp	C/T	0.493793	0.055364	intron-variant	NSMAF	GRCh38.p7	8:58634011	ATGAAAACCCTATCT[C/T]CAAGTCAAAAAGTAC	8439
rs7840932	snp	A/G	0.498369	0.0285077	intron-variant	NSMAF	GRCh38.p7	8:58589256	AGATATATTTTATAT[A/G]TATTTTTTAAACACA	8439
rs7841618	snp	C/T	0.305685	0.24372	intron-variant	NSMAF	GRCh38.p7	8:58610835	TAAAGCACAAAGATA[C/T]CTCTAGAATCCTTCA	8439
rs7844231	snp	G/T	0.49949	0.0159663	intron-variant	NSMAF	GRCh38.p7	8:58593473	ATGATAAAGACTAAA[G/T]AACGAGTAGCCTTAC	8439
rs10086028	snp	G/T	0.370974	0.218781	intron-variant	NSMAF	GRCh38.p7	8:58612325	actatgaggctggga[G/T]agcttctgggttgct	8439
rs10086130	snp	A/G	0.192088	0.2432	intron-variant	NSMAF	GRCh38.p7	8:58605399	CTCATAAACTAATAT[A/G]AGACCTGACTGAACA	8439
rs10086457	snp	C/G	0.293294	0.246223	intron-variant	NSMAF	GRCh38.p7	8:58605629	AAAGAGGCGATTCTA[C/G]AAATAGCATTTTTCT	8439
rs10087843	snp	C/T	0.413748	0.188909	intron-variant	NSMAF	GRCh38.p7	8:58621783	gcatgtatgtctttt[C/T]ttgaaaagtgtctgt	8439
rs10088312	snp	A/T	0	0	intron-variant	NSMAF	GRCh38.p7	8:58639015	aatgggtgggtgtgg[A/T]ggctcacgcctgtaa	8439
rs10088541	snp	A/G	0.411914	0.190483	intron-variant	NSMAF	GRCh38.p7	8:58618348	TAATATGAAGCTATA[A/G]GATGatattatgatt	8439
rs10090212	snp	A/G	0.43309	0.17023	intron-variant	NSMAF	GRCh38.p7	8:58643597	GAGTAAAATGGCGCA[A/G]TCTCAGCTCAAGTAA	8439
rs10090837	snp	G/T	0.417683	0.185425	intron-variant	NSMAF	GRCh38.p7	8:58621978	ctttagtttaattag[G/T]tctcatttgtcaatt	8439
rs10091952	snp	A/G	0.37138	0.218556	intron-variant	NSMAF	GRCh38.p7	8:58631854	GCAGACAGGGAAGGA[A/G]GCTAATCCAAGTGCT	8439
rs10093782	snp	A/G	0.191147	0.242974	intron-variant	NSMAF	GRCh38.p7	8:58607161	AAAAAATGAATTTCT[A/G]TTGGTGTCGAATTAA	8439
rs10098355	snp	A/G	0.19334	0.243495	intron-variant	NSMAF	GRCh38.p7	8:58638508	atcatccacaaaggt[A/G]ccaaaaacacacaat	8439
rs10099231	snp	C/T	0.19334	0.243495	intron-variant	NSMAF	GRCh38.p7	8:58626256	ggcacttgcctcgcc[C/T]ggctaattttttgta	8439
rs10103176	snp	A/G			intron-variant	NSMAF	GRCh38.p7	8:58654904	caatggcacaatctc[A/G]gctcactgcaacctc	8439
rs10103279	snp	C/T			intron-variant	NSMAF	GRCh38.p7	8:58654897	tggagtgcaatggca[C/T]aatctcagctcactg	8439
rs10107530	snp	A/T	0.380138	0.213458	intron-variant	NSMAF	GRCh38.p7	8:58589208	TAACAGATATTATAT[A/T]TTAAATATAAATAAT	8439
rs10111180	snp	C/T	0.43132	0.172114	intron-variant	NSMAF	GRCh38.p7	8:58599197	TGCTAAATATTCACC[C/T]AATGCTAAATAAAAT	8439
rs10112330	snp	C/T	0.414245	0.188477	intron-variant	NSMAF	GRCh38.p7	8:58638012	agaaattaacattga[C/T]attgacccacaaaat	8439
rs10113323	snp	A/G	0.394354	0.204112	intron-variant	NSMAF	GRCh38.p7	8:58642147	TTTACTTTAGCTTGT[A/G]TTTAAACAAATACCA	8439
rs10113667	snp	A/T	0.369346	0.219673	intron-variant	NSMAF	GRCh38.p7	8:58612326	ctatgaggctgggag[A/T]gcttctgggttgctg	8439
rs10113830	snp	A/C	0.398903	0.200818	intron-variant	NSMAF	GRCh38.p7	8:58635245	AATACAGATAAAAGT[A/C]ATTAAATATATACAG	8439
rs10504257	snp	A/C	0.0901694	0.192235	intron-variant	NSMAF	GRCh38.p7	8:58631628	AATCAGAACATTATC[A/C]ATCAAAAGTTTTAAA	8439
rs10656601	in-del	-/AT/ATAT	0.574554	0.104622	intron-variant	NSMAF	GRCh38.p7	8:58604557	ACATAGATATATATA[-/AT/ATAT]ATATATATATATAAA	8439
rs10710122	in-del	-/A	0.135143	0.222054	intron-variant	NSMAF	GRCh38.p7	8:58592566	GAGAAAAACAAACAG[-/A]AAAAAACAAAAGCTT	8439
rs10957061	snp	C/T	0.0418186	0.138422	intron-variant	NSMAF	GRCh38.p7	8:58611232	ACTTTAAGATAACTA[C/T]AGTAAATATGATAAA	8439
rs10957062	snp	A/C	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58611491	TCAGCCATGATTATG[A/C]CACTGCACTCCAGCC	8439
rs10957063	snp	A/G	0.412583	0.189912	intron-variant	NSMAF	GRCh38.p7	8:58630741	TCAGCACATGCAAGT[A/G]TTTCTTGTCCGTAAA	8439
rs11337086	in-del	-/A			intron-variant	NSMAF	GRCh38.p7	8:58645114	ACTTAAAGTATAATT[-/A]AAAAAAAAAAAAAAA	8439
rs11431046	in-del	-/T	0	0	intron-variant	NSMAF	GRCh38.p7	8:58624036	TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTTGT	8439
rs11774558	snp	A/T	0.379746	0.213696	intron-variant	NSMAF	GRCh38.p7	8:58588367	GTACAGTTTCCATTT[A/T]ATTTTTCTCCAGAGA	8439
rs11774998	snp	C/G	0.412917	0.189626	intron-variant	NSMAF	GRCh38.p7	8:58636784	ctgtagtttgccaag[C/G]cctgctgtgaatcca	8439
rs11777487	snp	C/T	0.00199481	0.0315187	intron-variant	NSMAF	GRCh38.p7	8:58635128	CTACAAGTAATTTCA[C/T]TCATGCACATATATA	8439
rs11780640	snp	G/T	0	0	intron-variant	NSMAF	GRCh38.p7	8:58603001	CTTCAAGAAGTATGG[G/T]GGAAAAAACATACAT	8439
rs11782455	snp	A/G	0.379354	0.213933	intron-variant	NSMAF	GRCh38.p7	8:58589304	TCCTTACACTCACAC[A/G]CTTTGTGAAAAAGAG	8439
rs11784708	snp	A/C	0.0248432	0.108648	intron-variant	NSMAF	GRCh38.p7	8:58609426	ACTCAAACTTCAGAG[A/C]CTACACATCACGATT	8439
rs11785141	snp	C/T	0.426528	0.177025	intron-variant	NSMAF	GRCh38.p7	8:58588466	CCCGCAGGTCTAAAT[C/T]GGGGTGGGGGTGTTC	8439
rs11985566	snp	C/T	0.416708	0.186302	intron-variant	NSMAF	GRCh38.p7	8:58627555	tcagtagcactgcta[C/T]acaccaacaacggcc	8439
rs11994921	snp	C/T	0.411914	0.190483	intron-variant	NSMAF	GRCh38.p7	8:58616988	AAATATCTAGGAATA[C/T]GTCCAACAAAAGATG	8439
rs11994937	snp	C/T	0.0792508	0.182605	intron-variant	NSMAF	GRCh38.p7	8:58596021	TGCAACAATTTTGTT[C/T]TGGTGTGGGGTGGGG	8439
rs11995355	snp	A/G	0.0364509	0.129988	intron-variant	NSMAF	GRCh38.p7	8:58591248	GCAGAAAGTTACAGG[A/G]AGGAAAATAGCAATT	8439
rs12056696	snp	A/T	0.00358779	0.0422022	intron-variant	NSMAF	GRCh38.p7	8:58601154	AAAAAGCCTGAGAGG[A/T]ATAGATAGAACAATT	8439
rs12171634	snp	G/T	0.41141	0.19091	intron-variant	NSMAF	GRCh38.p7	8:58626092	tccattatataattc[G/T]ttttttttttttttt	8439
rs12171670	snp	C/T	0.419296	0.183954	intron-variant	NSMAF	GRCh38.p7	8:58626161	tggagtgcagtggcg[C/T]gatcttggctctctg	8439
rs12334684	snp	A/G	0.493013	0.058691	intron-variant	NSMAF	GRCh38.p7	8:58628827	ttggcaggcattttt[A/G]tttgtttgttttatt	8439
rs12674724	snp	A/G	0.461259	0.133677	intron-variant	NSMAF	GRCh38.p7	8:58600396	TTGGGAGGCCAAGGC[A/G]GGTGGATCACGAAGT	8439
rs12677290	snp	A/G	0.469295	0.120041	intron-variant	NSMAF	GRCh38.p7	8:58585631	AGAACAAAGATCAAG[A/G]CAACTGCAGTAGCTG	8439
rs12679938	snp	G/T	0.34437	0.231505	intron-variant	NSMAF	GRCh38.p7	8:58586126	CAAAATCCTTGTACT[G/T]AAGCAATGACTATCC	8439
rs12682397	snp	A/G			intron-variant	NSMAF	GRCh38.p7	8:58624062	tttttttttttttga[A/G]acagagtcttgttct	8439
rs12682645	snp	G/T	0	0	intron-variant	NSMAF	GRCh38.p7	8:58635026	TGAAGAAGCTCATTA[G/T]GGATCACATCTTTTT	8439
rs13248968	snp	C/T	0	0	intron-variant	NSMAF	GRCh38.p7	8:58642822	CTCCAAAAGACTCTC[C/T]TAGGTTATAATCCTC	8439
rs13251087	snp	G/T			intron-variant	NSMAF	GRCh38.p7	8:58642846	AATCCTCAATAAAAG[G/T]Ctaaataaaatttac	8439
rs13253245	snp	C/T	0.0182019	0.0936463	intron-variant	NSMAF	GRCh38.p7	8:58630363	GTATTATAATTCACA[C/T]TGGAACAAAAGAGCT	8439
rs13263085	snp	A/C			intron-variant	NSMAF	GRCh38.p7	8:58640537	AATAGTATACTAATA[A/C]CAACAATATTGCAAC	8439
rs13263086	snp	A/C	0	0	intron-variant	NSMAF	GRCh38.p7	8:58640540	AGTATACTAATAACA[A/C]CAATATTGCAACTGG	8439
rs13263515	snp	A/G			intron-variant	NSMAF	GRCh38.p7	8:58640425	TTTTCTTTTATACTG[A/G]AAAATCTGAGTCTTG	8439
rs13265063	snp	G/T			intron-variant	NSMAF	GRCh38.p7	8:58640400	TTCTTTAATATTACA[G/T]GTATGTCTCTTTTCT	8439
rs13265070	snp	G/T			intron-variant	NSMAF	GRCh38.p7	8:58640406	AATATTACATGTATG[G/T]CTCTTTTCTTTTATA	8439
rs13265082	snp	A/T			intron-variant	NSMAF	GRCh38.p7	8:58640418	ATGTCTCTTTTCTTT[A/T]ATACTGGAAAATCTG	8439
rs13270855	snp	C/T	0.12932	0.218944	upstream-variant-2KB	NSMAF	GRCh38.p7	8:58659942	GGCCAGCGGCCAGAC[C/T]AGGATCCGACCTCAC	8439
rs13438863	snp	C/T	0.0520825	0.152737	intron-variant	NSMAF	GRCh38.p7	8:58635973	TCAGTGCTCAATATA[C/T]ATGTACTGAATAGAT	8439
rs13439297	snp	A/T	0.0460142	0.144533	intron-variant	NSMAF	GRCh38.p7	8:58599685	CTAAGCAATAAAATA[A/T]TTACTGAAATTGCAC	8439
rs16923584	snp	A/G	0.0162398	0.0886349	intron-variant	NSMAF	GRCh38.p7	8:58588824	TAACTATAATCAACT[A/G]ATATTTCTGATCATG	8439
rs16923588	snp	A/G	0.472285	0.114409	intron-variant	NSMAF	GRCh38.p7	8:58595517	AAGACCCTAACTTTT[A/G]CCAGGACTATCAGCT	8439
rs16923594	snp	C/T	0.44546	0.155869	intron-variant	NSMAF	GRCh38.p7	8:58598309	GGAAGAAGATAAGCA[C/T]TGAAACTGAAGAGAA	8439
rs16923600	snp	A/C	0.0166325	0.0896639	intron-variant	NSMAF	GRCh38.p7	8:58601626	AAAAGAAATCATAAC[A/C]TAGATATACCATATT	8439
rs16923629	snp	A/C	0.254664	0.249956	intron-variant	NSMAF	GRCh38.p7	8:58651441	GCTGGACTCTAGAAA[A/C]TTACATTCTCCCTGA	8439
rs16923631	snp	A/G	0.193653	0.243567	intron-variant	NSMAF	GRCh38.p7	8:58652514	AGCCACACATGCTGA[A/G]CTGGGATGAGTGAGC	8439
rs16923635	snp	A/C/G	0.145978	0.227331	intron-variant	NSMAF	GRCh38.p7	8:58653093	AGGATGGGGGCACAG[A/C/G]AGTTAAGTGTTCCAA	8439
rs16923636	snp	A/G	0.101301	0.200969	intron-variant	NSMAF	GRCh38.p7	8:58653186	ATGCTTATGTTTTAA[A/G]GATAAGCATTAGAAA	8439
rs16923637	snp	G/T	0.332106	0.236133	intron-variant	NSMAF	GRCh38.p7	8:58655326	ATCCCAACACTCCAC[G/T]GTGGATAGTAAAGCA	8439
rs17206144	snp	C/T	0.031825	0.122064	intron-variant	NSMAF	GRCh38.p7	8:58603470	TAACGTGTAGACCAT[C/T]CCTGTGCATTCTTGA	8439
rs17206746	snp	A/T	0.372189	0.218105	intron-variant	NSMAF	GRCh38.p7	8:58631693	TGCTTTAGTATTAGT[A/T]CTAGTATGGCTTTAA	8439
rs17265530	snp	A/G	0.0322114	0.122752	intron-variant	NSMAF	GRCh38.p7	8:58602214	AATTCAAATATACAC[A/G]TTTACTTCCACAAAA	8439
rs17272151	snp	A/G	0.370365	0.219117	intron-variant	NSMAF	GRCh38.p7	8:58608152	CAGGTTAGATTGTGG[A/G]GTGATAAGAAATATA	8439
rs17272647	snp	A/G	0.0185938	0.0946107	intron-variant	NSMAF	GRCh38.p7	8:58631870	GCTAATCCAAGTGCT[A/G]ATTTTTTAAGAAACG	8439
rs17273109	snp	C/T	0.15665	0.231917	intron-variant	NSMAF	GRCh38.p7	8:58655616	GCCATCCCTGACAAA[C/T]CCAAGGAAGACATGT	8439
rs28373260	snp	C/T			intron-variant	NSMAF	GRCh38.p7	8:58585332	GTTTTTTTTTTTTCT[C/T]TTTTTTTACTATTCT	8439
rs28429099	snp	A/T	0.410568	0.191619	intron-variant	NSMAF	GRCh38.p7	8:58632503	GAAGCAGTTTTCCAC[A/T]TGGCTTCCTGGACAC	8439
rs28489122	snp	A/G	0.436408	0.16659	intron-variant	NSMAF	GRCh38.p7	8:58632795	CCCCTTGGAGTTCTC[A/G]TGGCCATCTTAAATC	8439
rs28507102	snp	A/C			intron-variant	NSMAF	GRCh38.p7	8:58598489	AAGACTCTGTCTCAA[A/C]CAAAAAAAAAAAAAA	8439
rs28548238	snp	A/G	0.192715	0.243348	intron-variant	NSMAF	GRCh38.p7	8:58645910	GCCAGGCGTGGTGGC[A/G]GGCGCCTATAATCCC	8439
rs28623575	snp	A/C	0.405082	0.196086	intron-variant	NSMAF	GRCh38.p7	8:58592917	CAAAAACAACAACAA[A/C]AAAAAAAAAACCTCT	8439
rs28655100	snp	C/T			intron-variant	NSMAF	GRCh38.p7	8:58585330	GGGTTTTTTTTTTTT[C/T]TCTTTTTTTACTATT	8439
rs28655813	snp	C/T			intron-variant	NSMAF	GRCh38.p7	8:58654954	ATTCTCTTGTCTCAG[C/T]CTCCCGAGTAGCTGG	8439
rs28674507	snp	A/G			intron-variant	NSMAF	GRCh38.p7	8:58654969	TCTCCCGAGTAGCTG[A/G]GATTACAGGTGTGTG	8439
rs28686801	snp	A/G	0.000798403	0.0199641	intron-variant	NSMAF	GRCh38.p7	8:58654960	TTGTCTCAGTCTCCC[A/G]AGTAGCTGGGATTAC	8439
rs28688734	snp	A/G	0.0248432	0.108648	intron-variant	NSMAF	GRCh38.p7	8:58598567	TTCCATAGGAATTGA[A/G]GCCACTGTTCTATCA	8439
rs28697918	snp	A/T	0.0228947	0.104514	intron-variant	NSMAF	GRCh38.p7	8:58591471	ATTTTCTTGTGTAAC[A/T]GAAACCTTCCTTTTT	8439
rs28710949	snp	C/T			intron-variant	NSMAF	GRCh38.p7	8:58654911	ACAATCTCAGCTCAC[C/T]GCAACCTCTGCCTCC	8439
rs28755983	snp	C/T	0.409891	0.192184	intron-variant	NSMAF	GRCh38.p7	8:58633019	TGGATTCCTGGAACA[C/T]CCCAATAGGTCTCCT	8439
rs28819228	snp	G/T	0.485324	0.0843964	intron-variant	NSMAF	GRCh38.p7	8:58639722	TGTCCATTGATAGAT[G/T]AATGAATAAAGAAAA	8439
rs28886919	snp	A/G	0.415235	0.18761	intron-variant	NSMAF	GRCh38.p7	8:58621501	GCTGGGTCAAATGGT[A/G]GCTCTGTTTTAAGTT	8439
rs33942423	in-del	-/A/AA/AAA/AAAA/AAAAA	0.737074	0.120428	intron-variant	NSMAF	GRCh38.p7	8:58601546	GTGTCTAGAATACAG[-/A/AA/AAA/AAAA/AAAAA]AAAAAAAAAAAAAAA	8439
rs34054274	in-del	-/T			intron-variant	NSMAF	GRCh38.p7	8:58624035	GGTATAGAGTTAGGA[-/T]TTTTTTTTTTTTTTT	8439
rs34092757	snp	A/C	0	0	upstream-variant-2KB	NSMAF	GRCh38.p7	8:58661287	TGAACCACCCCTCCC[A/C]TATGGTATATAAGCC	8439
rs34191934	in-del	-/G			intron-variant	NSMAF	GRCh38.p7	8:58659180	AAGGGGGTGCCCGCC[-/G]GGCAGCGTACTCACC	8439
rs34591986	in-del	-/A			intron-variant	NSMAF	GRCh38.p7	8:58652405	CCTGACCATGCCAGG[-/A]AAAAGGCTGGTGTTT	8439
rs34637164	snp	C/T	0.0289792	0.116832	synonymous-codon	NSMAF	GRCh38.p7	8:58597388	TTTACAAAATTTACC[C/T]GGGGAATCTGCCATA	8439
rs34638032	in-del	-/ACAC	0.492679	0.0600586	intron-variant	NSMAF	GRCh38.p7	8:58637018	ACTGATTAAGATTAT[-/ACAC]ACACACACACACACA	8439
rs34689462	in-del	-/T			intron-variant	NSMAF	GRCh38.p7	8:58651216	AAAAGACCTGGCTCA[-/T]TTTTATTATCCATGT	8439
rs34780319	in-del	-/T			intron-variant	NSMAF	GRCh38.p7	8:58609248	ATATTTCAAAATCTA[-/T]TTTCTTATTAATCAT	8439
rs34989196	in-del	-/G			intron-variant	NSMAF	GRCh38.p7	8:58655261	ACAAGTGTAAGCCAT[-/G]GCACCTAGGCAAGTA	8439
rs35037523	in-del	-/C			intron-variant	NSMAF	GRCh38.p7	8:58644144	GGGACTTGAGATGGG[-/C]CCTTAAGTTCCAGTG	8439
rs35129339	in-del	-/C			intron-variant	NSMAF	GRCh38.p7	8:58623443	AGTATCATAAACAGA[-/C]CATGAATTTATTTTT	8439
rs35188110	in-del	-/T			intron-variant	NSMAF	GRCh38.p7	8:58643431	CTGACTGAACAATGC[-/T]TAGGCTTCCCCACCT	8439
rs35189286	in-del	-/C			intron-variant	NSMAF	GRCh38.p7	8:58631208	AAATTCTCAGTAACA[-/C]CCCAGTAAATAATCT	8439
rs35190779	in-del	-/A			intron-variant	NSMAF	GRCh38.p7	8:58592685	TGAGGTCAGGAGTTC[-/A]AAGACCAACCTGGCC	8439
rs35209612	in-del	-/AAAA			intron-variant	NSMAF	GRCh38.p7	8:58600646	AAAAAAAAAAAAAAA[-/AAAA]GATTAGCACCACTAT	8439
rs35234411	in-del	-/C			intron-variant	NSMAF	GRCh38.p7	8:58595991	GTTTCAAAAACCTGA[-/C]CAGTTGCCTAAGAAT	8439
rs35286551	in-del	-/A			intron-variant	NSMAF	GRCh38.p7	8:58594609	CGTTTGACCATCACC[-/A]AAAGGACAAACTCTT	8439
rs35319550	in-del	-/G			intron-variant	NSMAF	GRCh38.p7	8:58645770	AATAGGCCAGGCGCA[-/G]CGGCTCACACCTGTA	8439
rs35328777	in-del	-/T			intron-variant	NSMAF	GRCh38.p7	8:58624059	TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTTGT	8439
rs35369541	in-del	-/C			intron-variant	NSMAF	GRCh38.p7	8:58591731	GCTTCAAGTGATCCG[-/C]CCCCTTCGGCCTCCC	8439
rs35393291	in-del	-/G			intron-variant	NSMAF	GRCh38.p7	8:58658289	TGAGTTACATAGTTA[-/G]GGGCTCAGTTATTTA	8439
rs35395804	snp	C/T			intron-variant	NSMAF	GRCh38.p7	8:58600576	CAGTGAGCTGAGATT[C/T]TGCTCACTGTACTCC	8439
rs35436008	snp	A/G/T	1.65512e-05	0.00287669	stop-gained, missense	NSMAF	GRCh38.p7	8:58635511	GGTTCAAAAATCACC[A/G/T]ATTTTGAACATATTT	8439
rs35465191	in-del	-/CT			intron-variant	NSMAF	GRCh38.p7	8:58598850	AACATGGTGAAACCG[-/CT]TCACGACCAAAAAAA	8439
rs35492874	in-del	-/C			intron-variant	NSMAF	GRCh38.p7	8:58590153	CTATCTTATACATTT[-/C]CCGAAAAATTAATGC	8439
rs35634753	in-del	-/C			intron-variant	NSMAF	GRCh38.p7	8:58586320	ATAAAGCAGTGTTAG[-/C]CATTGGCAAAACCTC	8439
rs35663505	in-del	-/C			intron-variant	NSMAF	GRCh38.p7	8:58644153	GATGGGCCTTAAGTT[-/C]CCAGTGTGTTGGAGG	8439
rs35666144	in-del	-/A			intron-variant	NSMAF	GRCh38.p7	8:58614705	GTCATTTGGACGCTG[-/A]AGTCAGCTGGGCCTG	8439
rs35668952	in-del	-/T			intron-variant	NSMAF	GRCh38.p7	8:58657258	AGAAATAAATGCTCA[-/T]TTTCAAGTTTCTTTT	8439
rs35747457	in-del	-/T			intron-variant	NSMAF	GRCh38.p7	8:58593034	TGGTTAACAAGGTCA[-/T]TACAAGTACAACTGT	8439
rs35776754	in-del	-/A			intron-variant	NSMAF	GRCh38.p7	8:58584456	GAATTATGGATATAG[-/A]AACAATGCAAATAAA	8439
rs35906151	in-del	-/A			intron-variant	NSMAF	GRCh38.p7	8:58619916	TTGAAGACATAAGTG[-/A]AAAAGGAAAATAAGG	8439
rs36011709	in-del	-/CC			intron-variant	NSMAF	GRCh38.p7	8:58654816	ACATATCTCAACTAT[-/CC]CTAAATTTCTTTTCT	8439
rs36053026	in-del	-/TAA	0.495708	0.0461266	intron-variant	NSMAF	GRCh38.p7	8:58600770	TCTCAGTGTGGTGGG[-/TAA]ATACCAAGTAAACTT	8439
rs36064879	in-del	-/G			intron-variant	NSMAF	GRCh38.p7	8:58632942	GTCAGCACATCTGTT[-/G]GGGTTTTCTTCAGAA	8439
rs36067275	snp	C/T	0.00276268	0.0370635	missense	NSMAF	GRCh38.p7	8:58599358	TCTGGAGAAAGTCCT[C/T]GGGACCTATTAGATT	8439
rs36136766	in-del	-/T			intron-variant	NSMAF	GRCh38.p7	8:58604550	ATATAACTACATAGA[-/T]ATATATAATATATAT	8439
rs55658192	snp	G/T	0.305436	0.243776	intron-variant	NSMAF	GRCh38.p7	8:58613520	AGTACTGAAAAATAC[G/T]AGAATTACCGAAAAG	8439
rs55719287	snp	C/T			intron-variant	NSMAF	GRCh38.p7	8:58605099	TAGCAACTTTGTAAA[C/T]TAGAATAATTTAATT	8439
rs55909077	snp	A/G	0.164873	0.23506	intron-variant	NSMAF	GRCh38.p7	8:58602520	TATTATTATTCTTCA[A/G]TATTAGCCTATTTGA	8439
rs55965030	in-del	-/T	0.402845	0.197835	intron-variant	NSMAF	GRCh38.p7	8:58595686	ACATTAAATTTTTGC[-/T]AAGTCAACTAAGTTA	8439
rs56249776	snp	C/T	0.379942	0.213577	intron-variant	NSMAF	GRCh38.p7	8:58590366	GGAGTAAATCTCCAG[C/T]TGGGGGCAGACTGGG	8439
rs56337961	snp	C/T	0.0295035	0.117819	intron-variant	NSMAF	GRCh38.p7	8:58618570	AAAAATATATACACA[C/T]ATATATATAATACAA	8439
rs56900658	in-del	-/A			intron-variant	NSMAF	GRCh38.p7	8:58635141	CATTCATGCACATAT[-/A]TAAGAATGTTCATTC	8439
rs57177969	in-del	-/AA/AAA/AAAA/AAAAG/AAAG/AAAT/AAG/AG/G	0.00173957	0.0294512	intron-variant	NSMAF	GRCh38.p7	8:58601560	GAAAAAAAAAAAAAA[lengthTooLong]TAGAGCTAAGTGTTG	8439
rs57204135	in-del	-/AGA			intron-variant	NSMAF	GRCh38.p7	8:58639320	AGAAGAAGAAGAAGA[-/AGA]CATACAAATGGCCAA	8439
rs57382087	snp	A/G			intron-variant	NSMAF	GRCh38.p7	8:58607519	GAATGAGAAACTCAA[A/G]GGCACTCTAGCCCTC	8439
rs57658577	snp	C/T	0.021333	0.101051	intron-variant	NSMAF	GRCh38.p7	8:58616224	AACAACAATCCTACA[C/T]AAACTTTTTCTGAAA	8439
rs57773582	snp	C/G	0.111224	0.207945	intron-variant	NSMAF	GRCh38.p7	8:58647440	CCCAGTAATACACTG[C/G]ACAGTGATATAGTTT	8439
rs57883071	snp	C/G	0.0023933	0.0345097	intron-variant	NSMAF	GRCh38.p7	8:58655096	CACCCACCTTGGCCT[C/G]CCAAAGTTCTGGGAC	8439
rs58238055	snp	A/G			intron-variant	NSMAF	GRCh38.p7	8:58654898	GGAGTGCAATGGCAC[A/G]ATCTCAGCTCACTGC	8439
rs58306865	snp	C/T			intron-variant	NSMAF	GRCh38.p7	8:58593690	AGTAAGGGATGCTTT[C/T]TGCTTTACAGCTATA	8439
rs58563498	snp	C/T			intron-variant	NSMAF	GRCh38.p7	8:58641741	ATAACTGCCAGTTCT[C/T]TTTGAAATGGTATCC	8439
rs58627447	snp	C/T	0.079696	0.183021	intron-variant	NSMAF	GRCh38.p7	8:58643097	GGGGCGAAAAAACAA[C/T]TTTCAGTTTATTTTT	8439
rs58863335	snp	A/G	0.180383	0.240111	intron-variant	NSMAF	GRCh38.p7	8:58657915	GAATTCTAACAAAGC[A/G]GCATATACATGGAAA	8439
rs58866790	snp	A/C	0.19334	0.243495	intron-variant	NSMAF	GRCh38.p7	8:58642571	CCGAATAATTGAGAG[A/C]AGAGGATACTGCATA	8439
rs59030019	snp	A/C/T	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58586102	CCTAATCTCCACATT[A/C/T]GTTTTCTTCAAAATC	8439
rs59063037	in-del	-/A			intron-variant	NSMAF	GRCh38.p7	8:58607151	TCAAAGGAGAAAAAA[-/A]TGAATTTCTATTGGT	8439
rs59104727	snp	C/T	0.110519	0.207473	intron-variant	NSMAF	GRCh38.p7	8:58638575	AAAACTAGATATCCC[C/T]GTGGAAAAAAAAAAG	8439
rs59269342	snp	A/C	0.0537552	0.154881	intron-variant	NSMAF	GRCh38.p7	8:58607751	ATCATGCCCCAGCAC[A/C]GCCTCCCAAGGACTC	8439
rs59589377	in-del	-/AAA			upstream-variant-2KB	NSMAF	GRCh38.p7	8:58660112	TGAAAAAAAAAAAAA[-/AAA]GACGGAAGTTAAAGG	8439
rs59606339	snp	A/C	0.191755	0.24312	missense, intron-variant	NSMAF	GRCh38.p7	8:58659297	GACCTGCACTGCCGG[A/C]TAGCTCGGCATGCCT	8439
rs59644857	snp	C/T	0.227074	0.248947	intron-variant	NSMAF	GRCh38.p7	8:58584375	AATTAAAAATAATTG[C/T]TTGGTACAAAGATCT	8439
rs60099840	in-del	-/T/TATA	0	0	intron-variant	NSMAF	GRCh38.p7	8:58604570	TAATATATATATATA[-/T/TATA]AACCTACTTTAAAAT	8439
rs60214509	in-del	-/T			intron-variant	NSMAF	GRCh38.p7	8:58588335	TAACTTGACATTTTC[-/T]TTTTTTTTTTTTTTA	8439
rs60289621	snp	C/G	0.156319	0.231784	intron-variant	NSMAF	GRCh38.p7	8:58646035	AACAAGAGCGAGACT[C/G]CGTCTCAAAATCATC	8439
rs60504120	snp	G/T	0.157972	0.232445	intron-variant	NSMAF	GRCh38.p7	8:58640868	CACCACACCTGAACT[G/T]TTTCATTTTCTCTTT	8439
rs60534391	snp	A/T	0.293551	0.246177	intron-variant	NSMAF	GRCh38.p7	8:58606769	CAGGCTTTCACCATG[A/T]ACTAGCTGGGAGCTT	8439
rs60567264	snp	A/C	0.42357	0.179927	intron-variant	NSMAF	GRCh38.p7	8:58655088	AAGTGATCCACCCAC[A/C]TTGGCCTCCCAAAGT	8439
rs60663073	in-del	-/G	0.110561	0.207501	intron-variant	NSMAF	GRCh38.p7	8:58638458	GCTGTACAGACCAAT[-/G]GAACACAATACATCC	8439
rs60780937	snp	C/T	0.152001	0.229992	intron-variant	NSMAF	GRCh38.p7	8:58596288	CCAGGAAGCTATTTC[C/T]CCATGCTTGAGAGAA	8439
rs61196735	in-del	-/C			intron-variant	NSMAF	GRCh38.p7	8:58592911	CAAAAACAAAAACAA[-/C]AACAACAAAAAAAAA	8439
rs61359641	in-del	-/CT	0.165853	0.235413	intron-variant	NSMAF	GRCh38.p7	8:58598849	CAACATGGTGAAACC[-/CT]GTCACGACCAAAAAA	8439
rs61542378	snp	C/T	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58631431	AGATGTTAATAGAGT[C/T]ACAAAATTTTATTGT	8439
rs61553196	in-del	-/CA			intron-variant	NSMAF	GRCh38.p7	8:58592917	CAAAAACAACAACAA[-/CA]AAAAAAAAACCTCTC	8439
rs62512000	snp	G/T			intron-variant	NSMAF	GRCh38.p7	8:58643552	TTTTTTTTTTTTTGG[G/T]ACGGAGTTTCACTCT	8439
rs62512001	snp	A/C/T	0.00119737	0.0244387	intron-variant	NSMAF	GRCh38.p7	8:58645112	GAACTTAAAGTATAA[A/C/T]TAAAAAAAAAAAAAA	8439
rs66472341	in-del	-/AA			intron-variant	NSMAF	GRCh38.p7	8:58601547	TGTCTAGAATACAGA[-/AA]AAAAAAAAAAAAATA	8439
rs67832316	in-del	-/A	0.431769	0.17164	intron-variant	NSMAF	GRCh38.p7	8:58640556	CAATATTGCAACTGG[-/A]AAAGTTTACAATTAC	8439
rs67992430	in-del	-/TAA			intron-variant	NSMAF	GRCh38.p7	8:58600771	CTCAGTGTGGTGGGA[-/TAA]TACCAAGTAAACTTA	8439
rs71250204	in-del	-/AAAAAAAAAAAAAA	0.0209421	0.100162	intron-variant	NSMAF	GRCh38.p7	8:58598491	GACTCTGTCTCAAAC[-/AAAAAAAAAAAAAA]AAAAAAAGAAAAAAA	8439
rs71521421	snp	G/T	0.5	0	intron-variant	NSMAF	GRCh38.p7	8:58606919	AGCACTTAATCAATG[G/T]TAATTTCTTCTCTTT	8439
rs71521422	snp	A/C	0.5	0	intron-variant	NSMAF	GRCh38.p7	8:58620051	GATATAAGGCAATAA[A/C]CAAGTAAGAGAATGG	8439
rs71521423	snp	C/T	0.00517822	0.0506191	intron-variant	NSMAF	GRCh38.p7	8:58632352	CATGACAGGTTTTCA[C/T]CCCTACCATATTATT	8439
rs71767302	in-del	-/T	0.499539	0.0151687	intron-variant	NSMAF	GRCh38.p7	8:58643535	CTCTAGGGACAGATC[-/T]TTTTTTTTTTTTTTG	8439
rs71942199	in-del	-/AAA			intron-variant	NSMAF	GRCh38.p7	8:58601558	CAGAAAAAAAAAAAA[-/AAA]AATAGAGCTAAGTGT	8439
rs72647443	snp	A/G	0.397994	0.201489	intron-variant	NSMAF	GRCh38.p7	8:58584812	TTTCTAATATTTCTG[A/G]TTTTTAGTAAGAGAT	8439
rs72647444	snp	C/T	0.00597247	0.0543191	intron-variant	NSMAF	GRCh38.p7	8:58591776	ACAGGTGTGAGTAAC[C/T]GTGCCCGGCCTCAAA	8439
rs72647445	snp	A/T	0.00835141	0.0640778	intron-variant	NSMAF	GRCh38.p7	8:58595434	TTTGGGGAGATTTTT[A/T]AAAATAAAGACAACA	8439
rs72647450	snp	G/T			intron-variant	NSMAF	GRCh38.p7	8:58608126	TTAGTTTGGGGTGGG[G/T]TGATATCTTTCAGGT	8439
rs72647451	snp	A/C	0.408017	0.193729	intron-variant	NSMAF	GRCh38.p7	8:58610673	AGTGAGTAAGGGCTG[A/C]AGAATGAAGAGAGAT	8439
rs72647454	snp	C/T	0.00716266	0.059414	intron-variant	NSMAF	GRCh38.p7	8:58624738	CTGTTGGGTAGAAAG[C/T]TCTGCATATCTGTTA	8439
rs72647462	snp	C/T	0.000798403	0.0199641	intron-variant	NSMAF	GRCh38.p7	8:58649393	ATGAGACTTAGGACT[C/T]TGGACTTGATGTTGA	8439
rs72647463	snp	C/T	0.0232847	0.105357	intron-variant	NSMAF	GRCh38.p7	8:58653159	TGATTAGCTTCAGAT[C/T]TTAAATTTAATATGC	8439
rs72647464	snp	A/C			intron-variant	NSMAF	GRCh38.p7	8:58655506	CTGGGCTCGAGTGAT[A/C]TTCCCACCTTTTAAT	8439
rs73240230	snp	A/T	0.02016	0.0983543	intron-variant	NSMAF	GRCh38.p7	8:58640236	GAGGTGATGGATATG[A/T]TAATTACTTTGATTG	8439
rs73240232	snp	C/G	0.0898077	0.191933	intron-variant	NSMAF	GRCh38.p7	8:58641665	GTCTCCTGTAGGATT[C/G]TTCCTAGTCTTTTAC	8439
rs73240235	snp	C/G	0.111224	0.207945	intron-variant	NSMAF	GRCh38.p7	8:58647542	GGTGATTGGATCATG[C/G]GGGTAGATCCCTCAT	8439
rs73240247	snp	C/G	0.117886	0.21224	upstream-variant-2KB	NSMAF	GRCh38.p7	8:58660504	TTGTTGAGATAATTG[C/G]TCGCATGATTTTTTT	8439
rs73240249	snp	A/G	0.0901694	0.192235	upstream-variant-2KB	NSMAF	GRCh38.p7	8:58660681	CCATACCCTCTAGCT[A/G]TCACTCTTCCTAACT	8439
rs73240250	snp	A/G	0.0944967	0.195752	upstream-variant-2KB	NSMAF	GRCh38.p7	8:58661030	TGGACCTATGTTTCC[A/G]TTTCTGTTGAGTGGA	8439
rs73240252	snp	A/T	0.0941369	0.195465	upstream-variant-2KB	NSMAF	GRCh38.p7	8:58661137	CTTCTGATTGACCCC[A/T]GTTCTGGGAAGGCCT	8439
rs73248892	snp	G/T	0.0314385	0.121371	intron-variant	NSMAF	GRCh38.p7	8:58592940	AAACCTCTCTCTCCT[G/T]TATTGTGAAAATCCA	8439
rs73248900	snp	C/T	0.0376037	0.131863	intron-variant	NSMAF	GRCh38.p7	8:58594412	TCACAGCATGTCTGC[C/T]GGATCTGTCCCAGCA	8439
rs73248901	snp	A/G	0.0119091	0.0762411	intron-variant	NSMAF	GRCh38.p7	8:58594595	CTTCTATTCCCCCTC[A/G]TTTGACCATCACCAA	8439
rs73250303	snp	C/T	0.114738	0.210248	intron-variant	NSMAF	GRCh38.p7	8:58594796	GAGAAAAGACAGCCA[C/T]TGTCATCATGAATCA	8439
rs73250333	snp	A/G	0.0998734	0.199905	intron-variant	NSMAF	GRCh38.p7	8:58615150	TTAAGAAGACATTAC[A/G]CATCTTAATGTATAT	8439
rs73250335	snp	C/G	0.149665	0.228982	intron-variant	NSMAF	GRCh38.p7	8:58615753	GGTGACCTAGACTTT[C/G]TTCTTAGAAAGTTAC	8439
rs73250339	snp	C/T	0.097727	0.198275	intron-variant	NSMAF	GRCh38.p7	8:58617087	TTGGTCTGTTCTTCT[C/T]AAATCTACAATCATT	8439
rs73250343	snp	C/T	0.147656	0.228091	intron-variant	NSMAF	GRCh38.p7	8:58618815	AACAAAAAATTATCT[C/T]CTCAGAAATACGATG	8439
rs73250346	snp	G/T	0.0150606	0.0854603	intron-variant	NSMAF	GRCh38.p7	8:58625755	CACTCCATATTTTTT[G/T]ATTGGGGAGTTTGAT	8439
rs73250347	snp	A/T	0.109108	0.206518	intron-variant	NSMAF	GRCh38.p7	8:58626645	TTCATATTTTTGCAA[A/T]TGCAAATTGTGTTAC	8439
rs73250349	snp	A/T	0.0901694	0.192235	intron-variant	NSMAF	GRCh38.p7	8:58626673	TACTATAACTATGTG[A/T]GTGCATGTGTCTTGT	8439
rs73250352	snp	C/G	0.0718919	0.175435	intron-variant	NSMAF	GRCh38.p7	8:58627059	TTGATGGGATTATTT[C/G]TTTTTTGCTTGCTGA	8439
rs73250359	snp	G/T	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58630398	TTTACTCAGACAACC[G/T]CACTTTTATTTCCTT	8439
rs73250362	snp	C/T	0.00597247	0.0543191	intron-variant	NSMAF	GRCh38.p7	8:58631347	AAAATCTGTGGCTCC[C/T]TTGGGTAATTTTGTT	8439
rs73684346	snp	C/T	0.00159617	0.0282053	intron-variant	NSMAF	GRCh38.p7	8:58595313	GACCACATCTTGTAC[C/T]GTGAAGTGACAGACT	8439
rs73684347	snp	C/T	0.00119737	0.0244387	intron-variant	NSMAF	GRCh38.p7	8:58601608	GACAAGTAGAAAAAG[C/T]CTAAAAGAAATCATA	8439
rs73684348	snp	A/G	0.0825414	0.185628	intron-variant	NSMAF	GRCh38.p7	8:58605161	CTTGAACATCATAAT[A/G]TAAGTATTTTCTCTG	8439
rs73684352	snp	A/G	0.00159617	0.0282053	intron-variant	NSMAF	GRCh38.p7	8:58631852	AAGCAGACAGGGAAG[A/G]AGGCTAATCCAAGTG	8439
rs73684353	snp	C/T	0.00159617	0.0282053	intron-variant	NSMAF	GRCh38.p7	8:58636257	ATAACCCCCTGGGAC[C/T]CTGCTGAATAACACA	8439
rs74356313	snp	A/C			intron-variant	NSMAF	GRCh38.p7	8:58619950	GGGGCCCTGCACTAC[A/C]AGATATCAATAGTTA	8439
rs74378476	snp	A/G	0.0448719	0.142907	intron-variant	NSMAF	GRCh38.p7	8:58657494	TGATGCAAGGGGATA[A/G]ACCCGGAAAAATCTG	8439
rs74390016	snp	A/G	0.0327778	0.123752	intron-variant	NSMAF	GRCh38.p7	8:58655288	AGTATCTAAACTTCT[A/G]CATTACCCAAGAAAT	8439
rs74411351	snp	A/C	0.177503	0.239258	intron-variant	NSMAF	GRCh38.p7	8:58655895	CTGGGCGAGAGTGAG[A/C]CTCCGTCTCAATAAA	8439
rs74444047	snp	C/T	0.0279526	0.114869	intron-variant	NSMAF	GRCh38.p7	8:58586209	TTGATTATGAGTTCA[C/T]TTTTATCTTAAATTA	8439
rs74566438	snp	C/T	0.0652144	0.168387	intron-variant	NSMAF	GRCh38.p7	8:58596428	TGGAAGCCTGTAGGT[C/T]TGAAGTTGTCTTAGG	8439
rs74639699	snp	C/T	0.0168055	0.0901129	intron-variant	NSMAF	GRCh38.p7	8:58647912	GGATATACGTAAAGA[C/T]ATGGAAGCAGCTTTG	8439
rs74675746	snp	C/T	0.00597247	0.0543191	intron-variant	NSMAF	GRCh38.p7	8:58638839	TCAAAAGACAACCTA[C/T]GGAATGGGAGAAAAT	8439
rs74784575	snp	A/G	0.00874735	0.0655527	intron-variant	NSMAF	GRCh38.p7	8:58647738	GCTTACCAGAAACCA[A/G]GCAGATGCTGGTGCC	8439
rs74799426	snp	A/T	0.0333695	0.124785	intron-variant	NSMAF	GRCh38.p7	8:58646561	GAAGGGATATAACCA[A/T]ATCATATTGTTTGAA	8439
rs74802209	snp	A/G	0.0603597	0.1629	intron-variant	NSMAF	GRCh38.p7	8:58648772	GTGTTAGGTGTGCAG[A/G]TGCACAGAATGCAAG	8439
rs74805916	snp	A/G	0.5	0	intron-variant	NSMAF	GRCh38.p7	8:58645128	TAAAAAAAAAAAAAA[A/G]AGAAATTGCAGTATC	8439
rs74853108	snp	G/T	0.155656	0.231515	intron-variant	NSMAF	GRCh38.p7	8:58636694	CAGCCACACACAGTA[G/T]GTACACAAATGGGAA	8439
rs74931651	snp	G/T			intron-variant	NSMAF	GRCh38.p7	8:58637797	AAATTTAACCAAGGA[G/T]GTAAAAAGTCTGTAC	8439
rs74972994	snp	C/T	0.0599851	0.162463	intron-variant	NSMAF	GRCh38.p7	8:58643851	TCTTTAGATATTCCC[C/T]TGTGATAACCAGCCC	8439
rs74999856	snp	A/G	0.133093	0.220981	intron-variant	NSMAF	GRCh38.p7	8:58629457	AATTTTCCTGAGCTC[A/G]TTAAGCATCTTTATG	8439
rs75030081	snp	C/G	0.0150606	0.0854603	intron-variant	NSMAF	GRCh38.p7	8:58602433	TTCCAAGTAAAACAA[C/G]AACAACAACAAAATT	8439
rs75109800	snp	A/G	0.00923794	0.0673322	intron-variant	NSMAF	GRCh38.p7	8:58635240	CCTAAAATACAGATA[A/G]AAGTCATTAAATATA	8439
rs75227414	snp	A/T	0.00676609	0.0577691	intron-variant	NSMAF	GRCh38.p7	8:58640336	TATTCATCAATTATA[A/T]CTCAATAAAGCTGGA	8439
rs75264318	snp	C/T	0.00159617	0.0282053	intron-variant	NSMAF	GRCh38.p7	8:58601967	CTGGTATAATTCCCC[C/T]AAGCCTTGGAGAAAC	8439
rs75266299	snp	A/G	0.0599851	0.162463	intron-variant	NSMAF	GRCh38.p7	8:58649233	GGGTTTCAGACTTCA[A/G]TGAGGCCTACTGCCC	8439
rs75330784	snp	C/T			intron-variant	NSMAF	GRCh38.p7	8:58617014	AGATGGCAGCATCTA[C/T]ATACTAAACAGAACA	8439
rs75450902	snp	C/T	0.0023933	0.0345097	intron-variant	NSMAF	GRCh38.p7	8:58587118	CAGTACTGTCAACTA[C/T]AGCATAAGATGCAGC	8439
rs75471338	snp	C/T	0.00636936	0.0560724	intron-variant	NSMAF	GRCh38.p7	8:58609328	ATCTCTAGCGACCCT[C/T]TACTAAAATAGGGAG	8439
rs75517496	snp	A/G	0.0391387	0.134304	intron-variant	NSMAF	GRCh38.p7	8:58611772	AAAAAATATATAGGA[A/G]TGTGTATCTGAGATC	8439
rs75535763	snp	A/G	0.0240643	0.107019	intron-variant	NSMAF	GRCh38.p7	8:58612355	TGAAGACATCTATGT[A/G]CCAGGAGGGTGATGT	8439
rs75546621	snp	A/T	0.00716266	0.059414	intron-variant	NSMAF	GRCh38.p7	8:58596185	AGAGTGCAGTTTGAA[A/T]CAGCATCACAAGATA	8439
rs75646495	snp	A/C	0.444444	0.157135	intron-variant	NSMAF	GRCh38.p7	8:58637042	CACACACACACACAC[A/C]CACACACAAACACAC	8439
rs75647812	snp	C/T	0.175897	0.238765	intron-variant	NSMAF	GRCh38.p7	8:58657952	TACAGGTTTCAAGGT[C/T]TGTGTGACACCACGG	8439
rs75669640	snp	C/G			intron-variant	NSMAF	GRCh38.p7	8:58596952	AAAAAAAAAAAAGAT[C/G]TGTATGTGGGTATAG	8439
rs75712986	snp	C/T	0.0441095	0.141807	intron-variant	NSMAF	GRCh38.p7	8:58637233	TTGATACCTTCCTTA[C/T]TTGCCAGTATGACAG	8439
rs75717007	snp	A/T	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58634597	AAGCAGATGAAACCC[A/T]GAGCCAAAAGAAAGT	8439
rs75763165	snp	C/T	0.0329836	0.124112	intron-variant	NSMAF	GRCh38.p7	8:58624903	AGTTCTATCAATGTT[C/T]GCTTCATATATTTAG	8439
rs75794523	snp	A/G	0.121022	0.21416	intron-variant	NSMAF	GRCh38.p7	8:58625813	TACTGTTGCCATTTT[A/G]ACTGTTTTCTGTCTT	8439
rs75827935	snp	A/G	0.0337553	0.125452	intron-variant	NSMAF	GRCh38.p7	8:58651438	TCAGCTGGACTCTAG[A/G]AAATTACATTCTCCC	8439
rs75851323	snp	C/G	0.0329836	0.124112	upstream-variant-2KB	NSMAF	GRCh38.p7	8:58660813	GGCCTTTTGTGTCTG[C/G]CTTCTTTCATTTAGC	8439
rs75868612	snp	A/G	0.02016	0.0983543	intron-variant	NSMAF	GRCh38.p7	8:58592307	CATTTCTCAGTCAGG[A/G]AACCAAAAAAATGGA	8439
rs75916717	snp	A/G	0.00597247	0.0543191	intron-variant	NSMAF	GRCh38.p7	8:58620228	CAGGAAAGACCTTCT[A/G]GAAGAACTGAGAGCA	8439
rs75989158	snp	A/G	0.5	0	intron-variant	NSMAF	GRCh38.p7	8:58638580	TAGATATCCCCGTGG[A/G]AAAAAAAAAGTGAAC	8439
rs76002125	snp	A/T	0.5	0	intron-variant	NSMAF	GRCh38.p7	8:58645114	ACTTAAAGTATAATT[A/T]AAAAAAAAAAAAAAA	8439
rs76043179	snp	C/T	0.5	0	intron-variant	NSMAF	GRCh38.p7	8:58592181	TTTAAGATGATTAAT[C/T]TGAGACATCCTACAA	8439
rs76050509	snp	A/G			intron-variant	NSMAF	GRCh38.p7	8:58608992	ACAAGTTTCAGCATG[A/G]ATATCTAAGTTTATA	8439
rs76103962	snp	A/G	0.095934	0.196885	intron-variant	NSMAF	GRCh38.p7	8:58625418	TATGTATGTATGTAT[A/G]TATATGTGTGAATGT	8439
rs76129781	in-del	-/GT	0.177824	0.239355	intron-variant	NSMAF	GRCh38.p7	8:58656024	TCTAAATCTTTTTTT[-/GT]TTTGTTTGTTTGAGA	8439
rs76143633	snp	A/C	0.5	0	intron-variant	NSMAF	GRCh38.p7	8:58596932	CAAGACTCCGTCTCA[A/C]AAAAAAAAAAAAAAA	8439
rs76143792	snp	G/T	0.0329836	0.124112	intron-variant	NSMAF	GRCh38.p7	8:58610640	TGAGTGGCAGGAGGA[G/T]GAGCAACCTATGATA	8439
rs76189774	snp	C/T	0.0596104	0.162024	intron-variant	NSMAF	GRCh38.p7	8:58636386	AGAAATTAATAATTC[C/T]TTAATGTCATCATGT	8439
rs76262616	snp	A/G	0.0520825	0.152737	intron-variant	NSMAF	GRCh38.p7	8:58635930	TGTTCTTTTGTGAGC[A/G]GTAAATATTTACTTT	8439
rs76279588	snp	A/T			intron-variant	NSMAF	GRCh38.p7	8:58596951	AAAAAAAAAAAAAGA[A/T]CTGTATGTGGGTATA	8439
rs76301119	snp	C/T	0.0283406	0.115616	intron-variant	NSMAF	GRCh38.p7	8:58630321	TCCACCTCACCCTTT[C/T]TTTTTTTTTAATCTG	8439
rs76354168	snp	A/T	0.0917425	0.193579	intron-variant	NSMAF	GRCh38.p7	8:58585855	GAAGTGATCATGAAC[A/T]TGTCTGTAAATGTCT	8439
rs76433721	snp	A/C	0.0244538	0.107838	utr-variant-3-prime	NSMAF	GRCh38.p7	8:58583817	ATTTATCTCTTAGCT[A/C]TTCTCTGCTACTTAG	8439
rs76522931	snp	A/G	0.125182	0.216612	upstream-variant-2KB	NSMAF	GRCh38.p7	8:58661736	AGAGAGAGAGACCTT[A/G]TCTCAAAAGAAAAAA	8439
rs76548657	snp	C/T	0.0599851	0.162463	intron-variant	NSMAF	GRCh38.p7	8:58643481	TGCCCCCAACATCTG[C/T]CTCATGGTTATCTGA	8439
rs76568131	snp	A/T	0.0569829	0.158885	intron-variant	NSMAF	GRCh38.p7	8:58653498	ACAATGGAAAATCCC[A/T]TACAAAGCAAATAAC	8439
rs76597186	snp	A/G	0.119387	0.213167	intron-variant	NSMAF	GRCh38.p7	8:58635551	CTCTGATTTTCCTAG[A/G]GATCCAAGTACAACA	8439
rs76620947	snp	A/G	0.0872718	0.189788	intron-variant	NSMAF	GRCh38.p7	8:58652922	AGAGAAAATAATTCC[A/G]TAACGAGGATATGAC	8439
rs76664593	snp	A/T			intron-variant	NSMAF	GRCh38.p7	8:58658926	TCCAACACAAGGTCC[A/T]CTGCGCGGGGAGCAA	8439
rs76751509	snp	A/C	0.183568	0.241012	intron-variant	NSMAF	GRCh38.p7	8:58604379	TCTTTTTATTGTAAT[A/C]TTGTTATAGTTAAAA	8439
rs76766121	snp	A/C	0.000747803	0.0193221	intron-variant	NSMAF	GRCh38.p7	8:58640141	TGACTACAGTCCATA[A/C]CACATCATACACTTG	8439
rs76775419	snp	C/G	0.0337553	0.125452	intron-variant	NSMAF	GRCh38.p7	8:58651336	CTTCCCTCCCAGAAA[C/G]AGTTCTCATGAATTT	8439
rs76795096	snp	G/T	0	0	intron-variant	NSMAF	GRCh38.p7	8:58627766	GGTCATTTTCACAAT[G/T]TTGAGTCTACCCATC	8439
rs76812722	snp	A/G	0.00597247	0.0543191	intron-variant	NSMAF	GRCh38.p7	8:58607701	CCATAAGTGTTTACC[A/G]TCAATAAACTGCTGG	8439
rs76937541	snp	C/T	0.0418186	0.138422	intron-variant	NSMAF	GRCh38.p7	8:58616880	TGAATTTAGAAGAGT[C/T]ATAGTATACAAGGCC	8439
rs77029767	snp	A/C/T	0.0422008	0.138995	intron-variant	NSMAF	GRCh38.p7	8:58651757	ATTACTGTTATCTAG[A/C/T]GCAGCGCTTCACAAA	8439
rs77059535	snp	G/T	0.0170251	0.090679	intron-variant	NSMAF	GRCh38.p7	8:58657714	CATGGGGCAGAGCAC[G/T]AAACAATTTGGGCAC	8439
rs77125463	snp	A/G	0.0596104	0.162024	intron-variant	NSMAF	GRCh38.p7	8:58650256	ACTTCCTAGTTCCAA[A/G]GGCAACTTTGGAAGT	8439
rs77192980	snp	C/T	0.0558544	0.157504	intron-variant	NSMAF	GRCh38.p7	8:58593123	AAAGATAAAGCACTT[C/T]GTCTGAGGCTATAAT	8439
rs77219624	snp	C/G	0.0596104	0.162024	intron-variant	NSMAF	GRCh38.p7	8:58636712	ACACAAATGGGAATG[C/G]CTGTGTTCCAGTAAA	8439
rs77564282	snp	A/G	0.0599851	0.162463	intron-variant	NSMAF	GRCh38.p7	8:58647359	TCTGAAATAAAGAAG[A/G]AATTAAGAAAACTGT	8439
rs77593073	snp	A/G	0.079617	0.182947	intron-variant	NSMAF	GRCh38.p7	8:58594566	CAATTTCTGGCAATT[A/G]GAAAACTCTTCTCCT	8439
rs77608120	snp	A/G	0.289942	0.246789	intron-variant	NSMAF	GRCh38.p7	8:58605893	TCCAAAAAAAAAAAA[A/G]AAAGAAAGAAACAAT	8439
rs77620684	snp	C/T	0.0596104	0.162024	intron-variant	NSMAF	GRCh38.p7	8:58637608	ACCCTAAGGATTCTA[C/T]CAAAAAAACTATTCA	8439
rs77724289	snp	C/T	0.0596104	0.162024	intron-variant	NSMAF	GRCh38.p7	8:58650934	AGCCACCATTTCTTC[C/T]ACCCACTTAACGTGG	8439
rs77736827	snp	C/T	0	0	intron-variant	NSMAF	GRCh38.p7	8:58598849	CCAACATGGTGAAAC[C/T]GTCACGACCAAAAAA	8439
rs77754084	snp	A/G	0.0599851	0.162463	intron-variant	NSMAF	GRCh38.p7	8:58645204	GTGAATGAGGGCAGT[A/G]GCCCCCAATTCTTTT	8439
rs77805388	snp	A/G	0.0174175	0.0916809	intron-variant	NSMAF	GRCh38.p7	8:58634941	TTCATTTCAAGCCTC[A/G]TAAATCATAAATCGT	8439
rs77807250	snp	A/G	0.0599851	0.162463	intron-variant	NSMAF	GRCh38.p7	8:58642210	GAATAATAAAAATAA[A/G]TGGATTTATCTACTG	8439
rs77940965	snp	C/G	0.5	0	intron-variant	NSMAF	GRCh38.p7	8:58607930	GGGAAAAAAAAATCA[C/G]CAAATCTTGCTTTCC	8439
rs77949515	snp	C/T	0.0298908	0.118541	intron-variant	NSMAF	GRCh38.p7	8:58655303	ACATTACCCAAGAAA[C/T]AGCTGTCATCCCAAC	8439
rs77976156	snp	A/C	0.0596104	0.162024	intron-variant	NSMAF	GRCh38.p7	8:58641387	CCTCATTCCATCTCT[A/C]TATTGTTCTTCTGAT	8439
rs77982702	snp	C/G	0.0584853	0.160693	intron-variant	NSMAF	GRCh38.p7	8:58630970	TCTACTATGTATTAA[C/G]CTGAAGCATAAAGAA	8439
rs77985891	snp	A/G	0.0799831	0.183287	intron-variant	NSMAF	GRCh38.p7	8:58593675	AACAATGGTGTATAT[A/G]GTAAGGGATGCTTTC	8439
rs78073005	snp	A/T	0.5	0	upstream-variant-2KB	NSMAF	GRCh38.p7	8:58660522	GCATGATTTTTTTTT[A/T]TATAACAGCTTTATT	8439
rs78087465	snp	C/G	0.0596104	0.162024	intron-variant	NSMAF	GRCh38.p7	8:58640592	ATTCTTTTTCAACTT[C/G]TTTGCAATACTTTTT	8439
rs78100978	snp	A/G	0.00597247	0.0543191	intron-variant	NSMAF	GRCh38.p7	8:58652244	AGAGATTACCTACAA[A/G]GAACAATTAGACTTA	8439
rs78187905	snp	A/T	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58641788	AGATCAATAGGTTAA[A/T]GCACATGTCATCTTA	8439
rs78203934	snp	A/C	0.5	0	intron-variant	NSMAF	GRCh38.p7	8:58605879	AGCGAGACTCAGCCT[A/C]CAAAAAAAAAAAAAA	8439
rs78232690	snp	A/G	0.5	0	intron-variant	NSMAF	GRCh38.p7	8:58644020	TTGTTGTATGGCTAC[A/G]GCAACAAATACATGA	8439
rs78267912	snp	C/T	0.0599851	0.162463	intron-variant	NSMAF	GRCh38.p7	8:58639917	TACTACATGATTTCA[C/T]GTAGACTCTAAAAGA	8439
rs78283377	snp	C/T	0.0599851	0.162463	intron-variant	NSMAF	GRCh38.p7	8:58646390	ATTTTATTTCTATGA[C/T]GCACAAGTAGCCTTC	8439
rs78313259	snp	C/T	0.0283406	0.115616	intron-variant	NSMAF	GRCh38.p7	8:58630380	GGAACAAAAGAGCTT[C/T]TCTTTACTCAGACAA	8439
rs78320292	snp	A/T	0.5	0	intron-variant	NSMAF	GRCh38.p7	8:58639288	GACTCCGTCTCAATA[A/T]AAAAAAAAAAAGAAG	8439
rs78351859	snp	G/T	0.5	0	intron-variant	NSMAF	GRCh38.p7	8:58651217	AAAAGACCTGGCTCA[G/T]TTTATTATCCATGTT	8439
rs78387563	snp	C/T	0.0711525	0.174681	intron-variant	NSMAF	GRCh38.p7	8:58652958	AGAAGGAATATTGAA[C/T]AAAAACAATGGTAAA	8439
rs78517028	snp	A/G	0.00159617	0.0282053	intron-variant	NSMAF	GRCh38.p7	8:58620501	ACTGGGGATGGGGGC[A/G]TCTTGAAAATTTTTA	8439
rs78533823	snp	A/T	0.0995161	0.199636	intron-variant	NSMAF	GRCh38.p7	8:58658208	GTACTAAACAAAGAA[A/T]CTCCACTCAAGCTCT	8439
rs78576678	snp	C/T	0.00716266	0.059414	intron-variant	NSMAF	GRCh38.p7	8:58610707	CAGGGAAATGGAAAG[C/T]CAGAGTTGAGACTGG	8439
rs78609537	snp	A/C			synonymous-codon	NSMAF	GRCh38.p7	8:58601494	GGAAGAGTAGTGACT[A/C]CCATACATGAACTTT	8439
rs78629641	snp	A/C	0.031825	0.122064	intron-variant	NSMAF	GRCh38.p7	8:58603110	AATTTGTTCACATGT[A/C]ACATCACAATTATAA	8439
rs78674858	snp	A/G	0.00914312	0.0669923	intron-variant	NSMAF	GRCh38.p7	8:58642482	CTTCTAGTTCAAATC[A/G]CATGACTCATTTTGA	8439
rs78681369	snp	A/G	0.120674	0.21395	intron-variant	NSMAF	GRCh38.p7	8:58634516	AATTCTTCTCTGAAC[A/G]CTTCAACACCCCAAG	8439
rs78734696	snp	A/G	0.0622301	0.165053	intron-variant	NSMAF	GRCh38.p7	8:58658624	CACTGGAAGATCTGT[A/G]GCTCTCACAATCAAA	8439
rs78831721	snp	C/T	0.0528381	0.153711	intron-variant	NSMAF	GRCh38.p7	8:58658060	TGTATATCAAAAAGG[C/T]CAATATGAGTATTGG	8439
rs78848156	snp	C/T	0.0603597	0.1629	intron-variant	NSMAF	GRCh38.p7	8:58648940	GCTGGAGTCCCCATA[C/T]ATAGTCCCCACCAAG	8439
rs78976045	snp	A/G	0.0573587	0.15934	intron-variant	NSMAF	GRCh38.p7	8:58653084	CTATAACTGAGGATG[A/G]GGGCACAGCAGTTAA	8439
rs79040519	snp	A/G	0.0596104	0.162024	intron-variant	NSMAF	GRCh38.p7	8:58638620	ATCCCATACATAAAA[A/G]TCTACTTGAAATGAA	8439
rs79040985	snp	C/T	0.0146672	0.084371	intron-variant	NSMAF	GRCh38.p7	8:58648192	GGGATCTGTGGAAGG[C/T]TGAACTTAAGAGTAA	8439
rs79046832	snp	A/C	0.0471551	0.14613	intron-variant	NSMAF	GRCh38.p7	8:58628431	AGTCACATACAAAAA[A/C]TATTCCTTCAGATAC	8439
rs79075701	snp	A/G	0.0596104	0.162024	intron-variant	NSMAF	GRCh38.p7	8:58636353	TCTTAATAAGTGACC[A/G]ATCATTAACACACTC	8439
rs79085330	snp	A/G			intron-variant	NSMAF	GRCh38.p7	8:58587105	CTTAGAGAAAAGGCA[A/G]TACTGTCAACTACAG	8439
rs79088831	snp	C/T	0.0599851	0.162463	intron-variant	NSMAF	GRCh38.p7	8:58647789	AGAACCATGAGCCAA[C/T]TAAGCCTCTTTCCAT	8439
rs79089199	snp	C/T	0.00159617	0.0282053	intron-variant	NSMAF	GRCh38.p7	8:58629888	CCTTTGAAGCAGTAG[C/T]GTGCTACCCAGCTCT	8439
rs79263920	snp	C/T	0.00398564	0.0444627	intron-variant	NSMAF	GRCh38.p7	8:58625515	TATCTTTCTGATAAA[C/T]TGACCCTTTTATCAT	8439
rs79270027	snp	A/G	0.118235	0.212457	intron-variant	NSMAF	GRCh38.p7	8:58635875	ATAGTCTTACAGACT[A/G]AGAATGCCTACACTC	8439
rs79339869	snp	A/C	0.0329836	0.124112	intron-variant	NSMAF	GRCh38.p7	8:58590657	TCCAAGTATTTTAAG[A/C]TAAAAATGAAATCAC	8439
rs79496598	snp	A/G	0.0603597	0.1629	intron-variant	NSMAF	GRCh38.p7	8:58648908	GTCTACGACAGTAGT[A/G]TGAAGGGGAAAAGTG	8439
rs79518213	snp	C/T			missense	NSMAF	GRCh38.p7	8:58623391	CCATGGCGGTTTGGT[C/T]ACCCAATTTGTCAAG	8439
rs79542143	snp	G/T	0.0130921	0.0798413	intron-variant	NSMAF	GRCh38.p7	8:58603831	TAGGCTTGGAAGAGA[G/T]GTACTACTGCTAATT	8439
rs79546377	snp	A/G	0.0329836	0.124112	intron-variant	NSMAF	GRCh38.p7	8:58616876	TGAGTGAATTTAGAA[A/G]AGTCATAGTATACAA	8439
rs79584150	snp	C/G	0.0221141	0.102801	intron-variant	NSMAF	GRCh38.p7	8:58596430	GAAGCCTGTAGGTTT[C/G]AAGTTGTCTTAGGTA	8439
rs79668053	snp	C/T	0.0225045	0.103662	intron-variant	NSMAF	GRCh38.p7	8:58593592	AGAGTGCCAACACAG[C/T]GCTCTCAACATGACA	8439
rs79697297	snp	C/G	0.00716266	0.059414	intron-variant	NSMAF	GRCh38.p7	8:58625614	CTAGCTCTGTTGTTT[C/G]ATTACCAAGCATGGA	8439
rs79745047	snp	C/T	0.16846	0.236329	intron-variant	NSMAF	GRCh38.p7	8:58591893	TTCTAACTTACACAA[C/T]GTGATGTCGGAATGA	8439
rs79745296	snp	C/G	0.0799831	0.183287	intron-variant	NSMAF	GRCh38.p7	8:58593936	CCAACAAGTGGACAG[C/G]GCACCTCTCATGGGC	8439
rs79758009	snp	G/T	0.0283406	0.115616	intron-variant	NSMAF	GRCh38.p7	8:58632569	CTTCCGTCTACTTTT[G/T]GACCTTGCTTTGTTC	8439
rs79764090	snp	G/T	0.5	0	intron-variant	NSMAF	GRCh38.p7	8:58591507	TTTTTTTTTTTTTTT[G/T]ACACAGTATCACTCT	8439
rs79799797	snp	C/T	0.0599851	0.162463	intron-variant	NSMAF	GRCh38.p7	8:58646993	TGTACAACACTTAAC[C/T]AGAACTTAAAATAGC	8439
rs79806631	snp	A/G/T	0.00776208	0.0618133	intron-variant	NSMAF	GRCh38.p7	8:58586049	CAGCTTCAGAATGTG[A/G/T]TTTACATTATTCTGG	8439
rs79878854	snp	A/G	0.00119737	0.0244387	intron-variant	NSMAF	GRCh38.p7	8:58641836	CACCTACATGGGGCT[A/G]TACCATTTTGCCCTA	8439
rs79989266	snp	A/T	0.0115144	0.0749975	intron-variant	NSMAF	GRCh38.p7	8:58631777	ACAAGATAGCAACAA[A/T]TACAAGATAAATAAA	8439
rs80127104	snp	A/C	0.5	0	intron-variant	NSMAF	GRCh38.p7	8:58637038	CACACACACACACAC[A/C]CACCCACACACAAAC	8439
rs80127371	snp	C/G	0.000798403	0.0199641	intron-variant	NSMAF	GRCh38.p7	8:58658448	TGGACACACTGGTTA[C/G]ACCAACATTACAGAT	8439
rs80145292	snp	C/T	0.5	0	intron-variant	NSMAF	GRCh38.p7	8:58655400	TAAAATAGAAATGTC[C/T]TTTTTTTTTTTTTCT	8439
rs80347765	snp	A/C/G	0.0422008	0.138995	intron-variant	NSMAF	GRCh38.p7	8:58651797	GCACACAATCAACTG[A/C/G]GGATCTTGTTAAAAT	8439
rs111250614	snp	A/G	0.5	0	intron-variant	NSMAF	GRCh38.p7	8:58585590	TGTTCCCTGATGGAA[A/G]AGGCAGGCTTGAGTT	8439
rs111266642	snp	A/C	0.00636936	0.0560724	intron-variant	NSMAF	GRCh38.p7	8:58646022	CTCCAGCCTAGGCAA[A/C]AAGAGCGAGACTCCG	8439
rs111319005	snp	A/G	0.00522792	0.0508589	missense	NSMAF	GRCh38.p7	8:58603374	TCAGCAGTGTGCTCC[A/G]CCACATGGTGCTCTG	8439
rs111348885	snp	A/G	0.5	0	intron-variant	NSMAF	GRCh38.p7	8:58648460	CTATGGAATAATTGC[A/G]TGCTAGAGAGATGAG	8439
rs111374814	snp	C/G	0.00557542	0.0525036	intron-variant	NSMAF	GRCh38.p7	8:58645468	AACTAAACAGCCTCA[C/G]AGAAAAAGCCAGGTC	8439
rs111387497	snp	C/T	0.130008	0.219321	intron-variant	NSMAF	GRCh38.p7	8:58598987	GCCAAGATTGTGTCA[C/T]TGCACTCCAGCCTGG	8439
rs111446513	in-del	-/C	0.5	0	intron-variant	NSMAF	GRCh38.p7	8:58589722	CTCAAATTACTAAAT[-/C]AAAATATTCAAAATT	8439
rs111479963	snp	C/T	0.0232847	0.105357	intron-variant	NSMAF	GRCh38.p7	8:58607108	ATTCCACAATGCTTT[C/T]GTAATGTCACCAAGT	8439
rs111495601	snp	C/T	0.5	0	intron-variant	NSMAF	GRCh38.p7	8:58601172	AGATAGAACAATTAG[C/T]GATTTTTTACATTTC	8439
rs111503399	in-del	-/AA	0.5	0	upstream-variant-2KB	NSMAF	GRCh38.p7	8:58660099	GTGTCCTCCATTGTG[-/AA]AAAAAAAAAAAAAGA	8439
rs111510937	snp	C/T	0.0236746	0.106192	intron-variant	NSMAF	GRCh38.p7	8:58593544	CATGGAAGCAGGAAG[C/T]AAAGATACTACCCTT	8439
rs111515165	snp	A/T	0.125182	0.216612	upstream-variant-2KB	NSMAF	GRCh38.p7	8:58661451	AAAATAAAAATTACC[A/T]GGGTACAGTGGCACA	8439
rs111516405	in-del	-/TG	0.5	0	intron-variant	NSMAF	GRCh38.p7	8:58625416	GTATGTATGTATGTA[-/TG]TATATATGTGTGAAT	8439
rs111524143	snp	A/C	0.0279526	0.114869	intron-variant	NSMAF	GRCh38.p7	8:58589722	CTCAAATTACTAAAT[A/C]AAAATATTCAAAATT	8439
rs111526931	snp	C/T			intron-variant	NSMAF	GRCh38.p7	8:58624127	GCTCACTGCAACCTC[C/T]GTCTCCTGGGTTCAA	8439
rs111551809	snp	A/G	0.0325976	0.123435	intron-variant	NSMAF	GRCh38.p7	8:58600452	ACATGGTGAAACCTC[A/G]TCTCTACTAAAAATA	8439
rs111561052	snp	A/C	0.00557542	0.0525036	intron-variant	NSMAF	GRCh38.p7	8:58654340	TGGCTCACCTGAGAT[A/C]GGGAGTTCGAGACCA	8439
rs111601968	snp	C/T	0.5	0	intron-variant	NSMAF	GRCh38.p7	8:58594554	ACATATTCCTGACAA[C/T]TTCTGGCAATTGGAA	8439
rs111613231	snp	A/G	0.5	0	intron-variant	NSMAF	GRCh38.p7	8:58617610	TCAAAACCACAACAA[A/G]ATACCATCTCATGCC	8439
rs111629575	snp	A/G	0.0150606	0.0854603	intron-variant	NSMAF	GRCh38.p7	8:58657650	CTGTCATTCAAATGC[A/G]TATTCTATGCATTGA	8439
rs111725014	snp	A/G	0.5	0	missense	NSMAF	GRCh38.p7	8:58599833	TTCAGGCTATTGACT[A/G]GAAAGCTCACATCAT	8439
rs111780262	snp	G/T	0.00517822	0.0506191	intron-variant	NSMAF	GRCh38.p7	8:58603849	ACTACTGCTAATTTG[G/T]CAATGACTACATATT	8439
rs111791325	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	SDCBP, NSMAF	GRCh38.p7	8:58583009	GCTGAGACTGAGTGT[C/T]AGGAAAATTGCTTCC	8439
rs111825363	snp	C/T	0.00517822	0.0506191	intron-variant	NSMAF	GRCh38.p7	8:58607992	CAAGGTGATATCTGG[C/T]TTCCCATTCTGCTCT	8439
rs111935811	snp	A/T	0.5	0	intron-variant	NSMAF	GRCh38.p7	8:58608572	AGGATCCTGGCCAGT[A/T]TTGGGAAGGGGTAAA	8439
rs112104200	snp	C/T	0.0107246	0.0724382	intron-variant	NSMAF	GRCh38.p7	8:58601799	TTTATGTGTCTCTTA[C/T]GCGATTTACCACAGA	8439
rs112124743	snp	G/T	0.5	0	intron-variant	NSMAF	GRCh38.p7	8:58601185	AGTGATTTTTTACAT[G/T]TCTTTACTTTTTTAT	8439
rs112174205	snp	C/T	0.0150606	0.0854603	intron-variant	NSMAF	GRCh38.p7	8:58655358	AAAAATTTAACAATT[C/T]GCCTACTTTAGTCTA	8439
rs112174664	snp	G/T			intron-variant	NSMAF	GRCh38.p7	8:58596804	GTGGTGGCGGGCGCC[G/T]GTAGTCCCAGCTACT	8439
rs112213500	in-del	-/A	0.415563	0.18732	intron-variant	NSMAF	GRCh38.p7	8:58645266	GTGGTTTTTCTATTT[-/A]AAAAAAAAGTGGAAC	8439
rs112226247	in-del	-/TCTTTAAATAATT	0.0103295	0.0711199	intron-variant	NSMAF	GRCh38.p7	8:58591909	GTGATGTCGGAATGA[-/TCTTTAAATAATT]TCTTCTGCACAGTAT	8439
rs112228649	snp	C/T	0.00517822	0.0506191	intron-variant	NSMAF	GRCh38.p7	8:58610578	GTTGAGCATGTAAAG[C/T]AACCTAAATGAACAT	8439
rs112233809	snp	A/T			splice-acceptor-variant	NSMAF	GRCh38.p7	8:58601537	TCCTGGTAGCGTGTC[A/T]AGAATACAGAAAAAA	8439
rs112251427	snp	A/G	0.00636936	0.0560724	intron-variant	NSMAF	GRCh38.p7	8:58657099	ACCTGTCAATCACAC[A/G]TCCTAAAAACATCTA	8439
rs112260176	snp	G/T	0.0146672	0.084371	intron-variant	NSMAF	GRCh38.p7	8:58653635	GATAACAATTCTAAG[G/T]TACTTACTGAATACA	8439
rs112333009	snp	C/G	0.00557542	0.0525036	intron-variant	NSMAF	GRCh38.p7	8:58637528	AAAAGAAAGAACAGG[C/G]ATCCAAATTGGAAAA	8439
rs112410678	snp	C/T	0.5	0	intron-variant	NSMAF	GRCh38.p7	8:58600025	GTTTCTGCAATACTA[C/T]ATATGAAAAAAAAAT	8439
rs112436112	snp	A/G	0	0	intron-variant	NSMAF	GRCh38.p7	8:58584523	GACAAAAGTTGGGAG[A/G]CAGATGTGAAGGAAA	8439
rs112471698	snp	C/T	0.0150606	0.0854603	intron-variant	NSMAF	GRCh38.p7	8:58657331	AATTAGCATGAGAGC[C/T]GCCAGTGAACTTACA	8439
rs112500913	snp	C/T	0.00557542	0.0525036	intron-variant	NSMAF	GRCh38.p7	8:58653609	TGATAAAAAATTCAA[C/T]TCACCAAGAAGATAA	8439
rs112518043	snp	A/G	0.5	0	intron-variant	NSMAF	GRCh38.p7	8:58590238	TAATTCCAGCTGTAG[A/G]GTTTTTTCCCAAATG	8439
rs112550046	in-del	-/CG	0	0	intron-variant	NSMAF	GRCh38.p7	8:58623300	ACCAGAAAAAAAGTA[-/CG]TTTATAAGTATTTAT	8439
rs112561291	in-del	-/C	0.5	0	intron-variant	NSMAF	GRCh38.p7	8:58590305	GACCTAGCCTGATGA[-/C]TCTCCAGGGTCCTGC	8439
rs112563457	snp	C/T	0.0287284	0.116357	upstream-variant-2KB	NSMAF	GRCh38.p7	8:58661607	GGGTGCAGTGGCACA[C/T]ACCTATAGTCCCAGC	8439
rs112566612	snp	C/T	0.0146672	0.084371	intron-variant	NSMAF	GRCh38.p7	8:58653944	AAGTAAGTGGGTAGG[C/T]TAGTAATACATTTTG	8439
rs112601288	snp	C/T	0.00557542	0.0525036	intron-variant	NSMAF	GRCh38.p7	8:58648574	TCCCATCACAGAGGG[C/T]CTAGGAGAGGAAAGA	8439
rs112613718	snp	C/G	0.0150606	0.0854603	intron-variant	NSMAF	GRCh38.p7	8:58657531	AATGGTAAATTTGGG[C/G]CTTAATAAAGTTGCC	8439
rs112618535	snp	A/C	0.125182	0.216612	upstream-variant-2KB	NSMAF	GRCh38.p7	8:58661370	TGAAGCTGGAGGATT[A/C]CTTGAAGCCAGGAGT	8439
rs112763617	snp	A/C	0.00517822	0.0506191	intron-variant	NSMAF	GRCh38.p7	8:58615254	GACAATTTTAACATC[A/C]TTCTCTCAGTGACTG	8439
rs112773679	snp	A/G	0.0023933	0.0345097	intron-variant	NSMAF	GRCh38.p7	8:58654037	TGTTTTTCATGTGAG[A/G]AAAAAAAACCCTATT	8439
rs112819868	snp	A/C	0.00716266	0.059414	intron-variant	NSMAF	GRCh38.p7	8:58617518	TATGAACAGACACTT[A/C]TCAAAAGAAGACATC	8439
rs112934124	snp	C/T	0.5	0	intron-variant	NSMAF	GRCh38.p7	8:58607472	GTTTTACACAGATCA[C/T]TCTAGCCTGAGCCCA	8439
rs112957608	snp	A/C/G	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58586278	TTTCTACCTGATACA[A/C/G]ATGCCACAAGTATAC	8439
rs112972156	snp	C/G	0.00279162	0.0372561	intron-variant	NSMAF	GRCh38.p7	8:58627321	AGACAAGGTTACCCA[C/G]TTTCACCACTTCTAT	8439
rs113021646	snp	A/G/T	0.000297	0.0121824	synonymous-codon	NSMAF	GRCh38.p7	8:58599239	TTACATACCATTATG[A/G/T]GCCCCAACTGCATCA	8439
rs113043285	snp	A/G	0.0023933	0.0345097	intron-variant	NSMAF	GRCh38.p7	8:58613151	GACTAGAAATTATAA[A/G]CATCTAAATATCTAA	8439
rs113047690	snp	C/T	0.0150606	0.0854603	intron-variant	NSMAF	GRCh38.p7	8:58654580	GAAAGAAAGTTAATA[C/T]TAGCATAATCAAGAA	8439
rs113053323	snp	C/T	0.5	0	intron-variant	NSMAF	GRCh38.p7	8:58621233	ATTAATTTGCTCCAG[C/T]GCCATCCGTGGCCTC	8439
rs113075924	snp	A/G	0.5	0	intron-variant	NSMAF	GRCh38.p7	8:58594413	CACAGCATGTCTGCC[A/G]GATCTGTCCCAGCAT	8439
rs113081985	snp	A/C	0	0	intron-variant	NSMAF	GRCh38.p7	8:58591600	CAAGCAATTCTTGTG[A/C]CTCAGCCTCCCGAAT	8439
rs113085598	snp	A/G	0.0376037	0.131863	intron-variant	NSMAF	GRCh38.p7	8:58600585	GAGATTCTGCTCACT[A/G]TACTCCAGCCTGGGC	8439
rs113098396	snp	G/T	0.00557542	0.0525036	intron-variant	NSMAF	GRCh38.p7	8:58604758	TTTGTTTGTTTGTTT[G/T]TTTGAGACAGGGTCT	8439
rs113201208	snp	A/T			intron-variant	NSMAF	GRCh38.p7	8:58589229	TATAAATAATATATA[A/T]ATATATATTATAGAT	8439
rs113211945	snp	C/T	0.105214	0.203807	intron-variant	NSMAF	GRCh38.p7	8:58645972	CTTGAACCTGGGAAG[C/T]AGAGGTTGCAGTGAG	8439
rs113231777	snp	C/T	0.00636936	0.0560724	intron-variant	NSMAF	GRCh38.p7	8:58641109	GTATTTTAGCAGAGA[C/T]GAGGTTTCACCGTGT	8439
rs113232919	snp	A/G	0.5	0	intron-variant	NSMAF	GRCh38.p7	8:58594134	ACTTTATGTGGAGGC[A/G]GCACATGCAAGTGCA	8439
rs113332653	snp	A/T	0.5	0	intron-variant	NSMAF	GRCh38.p7	8:58611180	AGAGAAAAGACTCTA[A/T]AGAAGGTGTGTCAGA	8439
rs113346339	snp	A/G	0.0279526	0.114869	intron-variant	NSMAF	GRCh38.p7	8:58598824	GGTCAGGAGTTTGAG[A/G]CCAACCTGGCCAACA	8439
rs113368984	snp	C/T	0.00755907	0.0610114	intron-variant	NSMAF	GRCh38.p7	8:58597298	CTCTAAGTAGCACAA[C/T]AGTATACGTCTTATC	8439
rs113426123	snp	A/C	0.0150606	0.0854603	intron-variant	NSMAF	GRCh38.p7	8:58656404	TATTTATAAACATCA[A/C]CAATAAATGGCACCA	8439
rs113439667	snp	C/T	0.00557542	0.0525036	intron-variant	NSMAF	GRCh38.p7	8:58641616	CTGCATAGTACTCCA[C/T]CATGTGGCCATTTCT	8439
rs113440553	snp	A/C	0.00557542	0.0525036	intron-variant	NSMAF	GRCh38.p7	8:58619641	TTGCATTCTATATAT[A/C]AACAATAAACAGAAA	8439
rs113493388	snp	A/C/G	3.30355e-05	0.00406407	missense	NSMAF	GRCh38.p7	8:58609693	GCGTCACCATTTCTG[A/C/G]TTTGCATTCCATGTG	8439
rs113530938	in-del	-/T	0.5	0	intron-variant	NSMAF	GRCh38.p7	8:58630318	CATTCCACCTCACCC[-/T]TTTTTTTTTTTTAAT	8439
rs113612498	snp	A/G	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58609322	GTCTAAATCTCTAGC[A/G]ACCCTTTACTAAAAT	8439
rs113703391	snp	A/G	0.00438332	0.0466095	intron-variant	NSMAF	GRCh38.p7	8:58639241	GTGAGCAGAGATCAC[A/G]CCACTGCACTTCAGC	8439
rs113738969	snp	A/G	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58595211	GTAAATCCAACACTC[A/G]TGGGGTATACATCAC	8439
rs113744183	snp	C/T	0.5	0	utr-variant-5-prime, intron-variant	NSMAF	GRCh38.p7	8:58659354	CCCGTCATCCAGTTC[C/T]TGTCCCCGGCAGGCT	8439
rs113798347	snp	C/G	0.0221141	0.102801	intron-variant	NSMAF	GRCh38.p7	8:58609296	TCTAGGAAATGCCTC[C/G]TAGAAGAAAGGTCTA	8439
rs113829551	snp	A/G	0.5	0	intron-variant	NSMAF	GRCh38.p7	8:58647314	GATTTAATTAAACGG[A/G]CCATTTTTAAGAAGC	8439
rs113847133	snp	A/G	0.0325976	0.123435	intron-variant	NSMAF	GRCh38.p7	8:58630173	AGTTTCATGCTCACC[A/G]GGGGTGCAGGATCCT	8439
rs113865246	snp	A/C	0.439224	0.163383	intron-variant	NSMAF	GRCh38.p7	8:58644655	ATTCTGCTACAAAGA[A/C]ACAGGCACACATATG	8439
rs113885233	snp	A/G	0.5	0	upstream-variant-2KB	NSMAF	GRCh38.p7	8:58661596	AAAAATTACCTGGGT[A/G]CAGTGGCACACACCT	8439
rs113969235	snp	A/G	0.0147201	0.0845185	intron-variant	NSMAF	GRCh38.p7	8:58586035	TCAGATATGAGTGAC[A/G]GCTTCAGAATGTGGT	8439
rs113997754	snp	C/T	1.65534e-05	0.00287688	intron-variant	NSMAF	GRCh38.p7	8:58601419	TGAAATAAAATTTAA[C/T]TGGGGGTAATGATAA	8439
rs114030808	snp	C/T	0.0626037	0.165477	intron-variant	NSMAF	GRCh38.p7	8:58643820	ACAAGCATGAGCCAC[C/T]GGCCCAGCCAACAGA	8439
rs114046880	snp	C/T	0.0275645	0.114116	intron-variant	NSMAF	GRCh38.p7	8:58622231	GTTGTTTAGAAAGGA[C/T]ATTTTAAAATTTATT	8439
rs114068917	snp	G/T	0.0517044	0.152246	intron-variant	NSMAF	GRCh38.p7	8:58647534	CGGTAGGAGGTGATT[G/T]GATCATGGGGGTAGA	8439
rs114103907	snp	C/T	0.0185938	0.0946107	intron-variant	NSMAF	GRCh38.p7	8:58633189	TGGCCCACAAGGCCC[C/T]GCATGACACGGTCCC	8439
rs114149618	snp	A/G	0.0115144	0.0749975	upstream-variant-2KB	NSMAF	GRCh38.p7	8:58660873	AGCATGTATCTGTAC[A/G]GTACTTCGTTCCTTT	8439
rs114194467	snp	A/G	0.0107246	0.0724382	intron-variant	NSMAF	GRCh38.p7	8:58619061	GACACATTCTAAGTA[A/G]GTCAGAAGAAGCTAA	8439
rs114232060	snp	C/T	0.0322114	0.122752	intron-variant	NSMAF	GRCh38.p7	8:58614577	AATTTGATTATCGGT[C/T]GTTGTCCTGCCTCTG	8439
rs114344173	snp	A/G	0.0119091	0.0762411	intron-variant	NSMAF	GRCh38.p7	8:58648260	GCAGCAAAGGGTTTC[A/G]GAACTGGTCTGGCTG	8439
rs114344372	snp	C/T	0.00318978	0.0398085	intron-variant	NSMAF	GRCh38.p7	8:58658339	ACTAAAACCTAATCA[C/T]ATCACCAAAAACATT	8439
rs114386215	snp	G/T	0.0221141	0.102801	intron-variant	NSMAF	GRCh38.p7	8:58597034	ACAGTGACTGGGAAG[G/T]CAGACTGGACAGCTA	8439
rs114418587	snp	A/G	0.0599851	0.162463	intron-variant	NSMAF	GRCh38.p7	8:58649700	TGTTTAAAAGAGTCC[A/G]GAGCCTCCTCCTCCT	8439
rs114434538	snp	A/C/G	0.0107246	0.0724382	intron-variant	NSMAF	GRCh38.p7	8:58594114	AAAGGAACTGCTCTA[A/C/G]GTTTACTTTATGTGG	8439
rs114473428	snp	G/T	0.0298908	0.118541	intron-variant	NSMAF	GRCh38.p7	8:58654016	AACATTTATTTCCTC[G/T]CCCGCTGTTTTTCAT	8439
rs114499353	snp	A/T	0.00358779	0.0422022	intron-variant	NSMAF	GRCh38.p7	8:58623552	GATATACCTATGGCT[A/T]CTTCCTAATATATAG	8439
rs114604639	snp	A/G	0.0298908	0.118541	intron-variant	NSMAF	GRCh38.p7	8:58656282	TTGGGGATTACAGGC[A/G]TGAGCCCTGTGTCTG	8439
rs114634049	snp	A/G	0.0333695	0.124785	intron-variant	NSMAF	GRCh38.p7	8:58645380	GATGAACACTAGTTT[A/G]CTGAGAATTATGGTT	8439
rs114644030	snp	A/G	0.0154538	0.0865337	intron-variant	NSMAF	GRCh38.p7	8:58636736	CAGTAAAACTTTACA[A/G]GAACAAGTGGCAGCT	8439
rs114672033	snp	A/G	0.00993419	0.0697739	intron-variant	NSMAF	GRCh38.p7	8:58590202	GCTCTCCTCCTATTT[A/G]CGCAGATTTTCTCAA	8439
rs114758390	snp	A/G	0.00676609	0.0577691	intron-variant	NSMAF	GRCh38.p7	8:58599684	TCTAAGCAATAAAAT[A/G]ATTACTGAAATTGCA	8439
rs114855446	snp	C/T	0.00159617	0.0282053	intron-variant	NSMAF	GRCh38.p7	8:58618962	CAGCAACTGGATACA[C/T]TAAAACGTTCACAGT	8439
rs114861835	snp	A/C/G	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58654787	GATAAAACTATGACT[A/C/G]TTCCTCAGAAGGAAA	8439
rs114872292	snp	C/G/T	0.00838764	0.064226	missense, intron-variant	NSMAF	GRCh38.p7	8:58659270	TCCGGGTGAGCTGCC[C/G/T]GCGGCCGCCGGGACC	8439
rs115075372	snp	C/T	0.00478085	0.0486577	intron-variant	NSMAF	GRCh38.p7	8:58657314	GAAATCTAAAATCCC[C/T]TAATTAGCATGAGAG	8439
rs115146661	snp	C/T	0.00119737	0.0244387	intron-variant	NSMAF	GRCh38.p7	8:58647453	TGGACAGTGATATAG[C/T]TTGGATGTTCTGTCC	8439
rs115177564	snp	C/T	0.00398564	0.0444627	intron-variant	NSMAF	GRCh38.p7	8:58591184	ACATGGTAGGTATAC[C/T]GTTGACATTTCAGCA	8439
rs115290812	snp	A/C/T			intron-variant	NSMAF	GRCh38.p7	8:58623301	ACCAGAAAAAAAGTA[A/C/T]TTATAAGTATTTATA	8439
rs115400736	snp	C/G	0.0596104	0.162024	intron-variant	NSMAF	GRCh38.p7	8:58644479	ATCAAGTGCTAGAGA[C/G]GATGTGGAGAAATAG	8439
rs115502177	snp	A/C	0.0596104	0.162024	intron-variant	NSMAF	GRCh38.p7	8:58649628	ATGCCTCAGCACCAT[A/C]CCCTTGGTAATAAGT	8439
rs115503834	snp	A/G	0.029116	0.117091	intron-variant	NSMAF	GRCh38.p7	8:58642708	AAGGTTTCAAGTTAC[A/G]ATTATAACTTTTAAA	8439
rs115531997	snp	C/T	0.0603597	0.1629	intron-variant	NSMAF	GRCh38.p7	8:58648391	AGCCCGGCCATGTGG[C/T]AGAGAAAGAAAAAGC	8439
rs115574277	snp	C/T	0.0383715	0.133092	intron-variant	NSMAF	GRCh38.p7	8:58658988	AGAATCAGGCCTTTC[C/T]GGCGGCCCCCCTCCC	8439
rs115787885	snp	C/T	0.000798403	0.0199641	intron-variant	NSMAF	GRCh38.p7	8:58634451	TGAAGTCAGCAAGTC[C/T]GTGCATCTTTGTTCC	8439
rs115888833	snp	C/T	0.0599851	0.162463	intron-variant	NSMAF	GRCh38.p7	8:58638702	TACAGAAAAGCTTCT[C/T]GGCATTGGTCTGGGC	8439
rs115890214	snp	C/T	0.0333695	0.124785	intron-variant	NSMAF	GRCh38.p7	8:58644434	ACCAGTTCAAGTCAC[C/T]GGACTTCCAAAAAGT	8439
rs115905537	snp	A/C/T	0.00517822	0.0506191	intron-variant	NSMAF	GRCh38.p7	8:58597646	AATAGGAGGGACTAA[A/C/T]CCTCAAATAATGACA	8439
rs115963376	snp	A/C	0.0279526	0.114869	downstream-variant-500B	SDCBP, NSMAF	GRCh38.p7	8:58583060	CAGGGCCAAAAGAAG[A/C]GCTGGTTCACACCTG	8439
rs115967796	snp	A/G	0.0283406	0.115616	intron-variant	NSMAF	GRCh38.p7	8:58630839	TCAGATTCAGCCTGT[A/G]GGACTATGTTTGCCC	8439
rs116055735	snp	A/C	0.0279526	0.114869	intron-variant	NSMAF	GRCh38.p7	8:58607415	ATTTTGCTTTGAGAC[A/C]TAGCTGCTATGAATG	8439
rs116201925	snp	C/T	0.0130921	0.0798413	intron-variant	NSMAF	GRCh38.p7	8:58631995	CCACTGGTCCTTACA[C/T]AGTATATTAATAACT	8439
rs116205331	snp	A/G	0.0193772	0.0965046	upstream-variant-2KB	NSMAF	GRCh38.p7	8:58661309	ATATAAGCCCTAAGG[A/G]GCTGGAGTGATGGCT	8439
rs116248212	snp	C/T	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58617137	GGAAGACTTTTGGGG[C/T]AGAAAAGGGTAAATT	8439
rs116254184	snp	A/G	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58639471	GTTGTTGGCAAGAGC[A/G]TGGAGAAAAGAGAAC	8439
rs116255551	snp	A/G	0.0599851	0.162463	intron-variant	NSMAF	GRCh38.p7	8:58644474	GCAGGATCAAGTGCT[A/G]GAGACGATGTGGAGA	8439
rs116358575	snp	C/T	0.0113802	0.0745694	intron-variant	NSMAF	GRCh38.p7	8:58599881	ATTAACTGAAAGTTT[C/T]GGGGAAAAATAAAAA	8439
rs116544617	snp	A/T	0.411724	0.190644	intron-variant	NSMAF	GRCh38.p7	8:58623302	CCAGAAAAAAAGTAT[A/T]TATAAGTATTTATAA	8439
rs116564295	snp	A/C	0.0103295	0.0711199	intron-variant	NSMAF	GRCh38.p7	8:58640930	TTTATTTATTGATTG[A/C]TTTATTTTTGAGACA	8439
rs116579426	snp	C/G	0.0596104	0.162024	intron-variant	NSMAF	GRCh38.p7	8:58643435	ACTGAACAATGCTAG[C/G]CTTCCCCACCTCTTC	8439
rs116612002	snp	C/T	0.0341408	0.126114	intron-variant	NSMAF	GRCh38.p7	8:58658572	TGTAACCTGCTTTGC[C/T]GGTATTCACTGATGA	8439
rs116638259	snp	C/T	0.0275645	0.114116	intron-variant	NSMAF	GRCh38.p7	8:58625930	TAAAATTTATTTTGA[C/T]AGTTTTTGTGGTACA	8439
rs116639554	snp	A/T	0.0325976	0.123435	intron-variant	NSMAF	GRCh38.p7	8:58632819	TTAAATCTCACATCC[A/T]ACTTGAAGCCTGCTC	8439
rs116670146	snp	A/G	0.0599851	0.162463	intron-variant	NSMAF	GRCh38.p7	8:58647556	GGGGGTAGATCCCTC[A/G]TGACTCAGCACCATC	8439
rs116673198	snp	A/G	0.0599851	0.162463	intron-variant	NSMAF	GRCh38.p7	8:58644670	AACAGGCACACATAT[A/G]TTTAATGCGGCACTG	8439
rs116987489	snp	A/G	0.0023933	0.0345097	intron-variant	NSMAF	GRCh38.p7	8:58639918	ACTACATGATTTCAC[A/G]TAGACTCTAAAAGAG	8439
rs117063745	snp	C/G	0.0314385	0.121371	intron-variant	NSMAF	GRCh38.p7	8:58602804	TTAATTTTCTTCTTT[C/G]ATTATTTCAGGACTT	8439
rs117087142	snp	A/G	0.00676609	0.0577691	intron-variant	NSMAF	GRCh38.p7	8:58627092	TGTTTGAGGTTCCTC[A/G]TAGATTCTGGATGTT	8439
rs117164295	snp	C/T	0.118235	0.212457	intron-variant	NSMAF	GRCh38.p7	8:58639278	GACAGAGTGAGACTC[C/T]GTCTCAATAAAAAAA	8439
rs117167909	snp	C/G	0.00636936	0.0560724	intron-variant	NSMAF	GRCh38.p7	8:58652324	CTGCAAAGTTTCAGG[C/G]AAAACTGCTATGATT	8439
rs117187681	snp	A/G	0.0494327	0.149241	intron-variant	NSMAF	GRCh38.p7	8:58643767	AACTCCCAACCTCAC[A/G]TAATCCACCCACCTC	8439
rs117413256	snp	C/T	0.0048914	0.0492115	synonymous-codon	NSMAF	GRCh38.p7	8:58595652	CAGGTCTTCAAAAGA[C/T]TCTTCACCTGGAGAG	8439
rs117475935	snp	C/T	0.00835141	0.0640778	intron-variant	NSMAF	GRCh38.p7	8:58649350	TTTTGATTTTACAGG[C/T]TCATAGGTGGAAAGA	8439
rs117607963	snp	A/C	0.40853	0.193309	intron-variant	NSMAF	GRCh38.p7	8:58592919	AAAACAACAACAACA[A/C]AAAAAAAACCTCTCT	8439
rs117703176	snp	A/G	0.0275645	0.114116	intron-variant	NSMAF	GRCh38.p7	8:58626866	CAAATCCATGCCAAC[A/G]TCTATTATTTTTTGA	8439
rs117884048	snp	C/T	0.0142736	0.0832652	intron-variant	NSMAF	GRCh38.p7	8:58633812	TGCCTGGTTGTATAC[C/T]TGACACAGGAAGCTT	8439
rs118011811	snp	C/T	0.0535932	0.154675	intron-variant	NSMAF	GRCh38.p7	8:58646840	AGACTCTTAGCCCTG[C/T]CCCTACATATTCCTA	8439
rs118039071	snp	A/T	0.00557542	0.0525036	intron-variant	NSMAF	GRCh38.p7	8:58609151	GCTCATAGTGCTCCT[A/T]CAGGAAAAATTCAGA	8439
rs118060071	snp	A/G	0.00676609	0.0577691	intron-variant	NSMAF	GRCh38.p7	8:58645315	TATCAGGCACAGTGG[A/G]GAGCAGGATTGTAGT	8439
rs118128651	snp	A/G	0.00636936	0.0560724	intron-variant	NSMAF	GRCh38.p7	8:58644086	TTGTGATAAGGACCA[A/G]GAAACATCAATGAGT	8439
rs137894141	snp	C/T	0.0599851	0.162463	intron-variant	NSMAF	GRCh38.p7	8:58644936	ATGGACACAGGGAGG[C/T]GAACATCACACACGG	8439
rs137945277	in-del	-/TCTT	0.371987	0.218218	intron-variant	NSMAF	GRCh38.p7	8:58629410	TCTTTGTTAATATTC[-/TCTT]TGTTAAAATTCTCAT	8439
rs137997625	snp	A/G	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58652526	TGAGCTGGGATGAGT[A/G]AGCCAAGGTTCCATC	8439
rs138006293	snp	C/T	0.00398564	0.0444627	intron-variant	NSMAF	GRCh38.p7	8:58624893	TTCTCCCTTCAGTTC[C/T]ATCAATGTTCGCTTC	8439
rs138041844	snp	C/T	0.000798403	0.0199641	intron-variant	NSMAF	GRCh38.p7	8:58605621	AGACCCACAAAGAGG[C/T]GATTCTACAAATAGC	8439
rs138116298	snp	A/G	0.00279162	0.0372561	intron-variant	NSMAF	GRCh38.p7	8:58594549	GCTTTACATATTCCT[A/G]ACAATTTCTGGCAAT	8439
rs138220588	snp	C/T	0.00874735	0.0655527	intron-variant	NSMAF	GRCh38.p7	8:58646670	ATGTAAAAATTATTA[C/T]AATTAAGTTGCATGA	8439
rs138228792	snp	C/T	0.000798403	0.0199641	intron-variant	NSMAF	GRCh38.p7	8:58639198	CTAAGGCAGGAGAAT[C/T]GCTTGAACCCGGAAG	8439
rs138347708	snp	C/T	0.00636936	0.0560724	intron-variant	NSMAF	GRCh38.p7	8:58634367	AGTGCTGGGAGCATG[C/T]TCTTCCCCTCCCCAT	8439
rs138352251	in-del	-/T			intron-variant	NSMAF	GRCh38.p7	8:58631299	AGGCACTTTTTTTTT[-/T]AAGTCAAAAAGTTAA	8439
rs138354390	snp	A/G	0.00279162	0.0372561	downstream-variant-500B	SDCBP, NSMAF	GRCh38.p7	8:58583331	TATACAGCTTACCTT[A/G]TTTGAAATTTAGAAG	8439
rs138393448	snp	A/G	0.00438332	0.0466095	intron-variant	NSMAF	GRCh38.p7	8:58647501	GAAATGTGATTCCCA[A/G]CGTTGAAGGTGGAGG	8439
rs138445971	in-del	-/TG	0.172997	0.237846	intron-variant	NSMAF	GRCh38.p7	8:58603725	TCCCTCCAAATGTGC[-/TG]TGTCTCCATGCATTT	8439
rs138504485	snp	A/G	8.24273e-05	0.00641926	synonymous-codon	NSMAF	GRCh38.p7	8:58609619	CGGGTAGCCGTTGAG[A/G]GGCTGAAAATACAGG	8439
rs138530641	snp	A/G	8.23811e-05	0.00641746	missense	NSMAF	GRCh38.p7	8:58586523	TGCATTAAGGTGGCC[A/G]TTGTGAGGTCCCAAA	8439
rs138534625	snp	A/T	0.00438332	0.0466095	intron-variant	NSMAF	GRCh38.p7	8:58620486	CTTTATCCTGAAGGC[A/T]CTGGGGATGGGGGCG	8439
rs138554941	snp	A/T	0.00398564	0.0444627	intron-variant	NSMAF	GRCh38.p7	8:58586156	CTCTCCTTGAAATGG[A/T]TCTAGCCCTTTCCAA	8439
rs138561357	snp	C/G	0.000798403	0.0199641	intron-variant	NSMAF	GRCh38.p7	8:58600160	GTTCTAACCATCTCT[C/G]TGAGTGTCCCACTTT	8439
rs138598489	snp	C/T	0.00159617	0.0282053	intron-variant	NSMAF	GRCh38.p7	8:58627783	TTGTGAAAATGACCA[C/T]ACTGCCTAAAGCAAG	8439
rs138599020	snp	A/G	0.0134861	0.0810011	intron-variant	NSMAF	GRCh38.p7	8:58644677	ACACATATGTTTAAT[A/G]CGGCACTGTTCACAA	8439
rs138612248	snp	A/G	0.0182019	0.0936463	intron-variant	NSMAF	GRCh38.p7	8:58607688	ACTTTCAGACATCCC[A/G]TAAGTGTTTACCGTC	8439
rs138626790	snp	C/T	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58615520	AATTATAAATCAGTA[C/T]CTATAAAATATCTAC	8439
rs138678600	snp	A/T	0.00874735	0.0655527	intron-variant	NSMAF	GRCh38.p7	8:58633985	AAATAACTAAAATGT[A/T]TAGTTTTATAATGAA	8439
rs138858711	snp	C/T			intron-variant	NSMAF	GRCh38.p7	8:58599563	TCACATTAAGGTCTC[C/T]CAAATATATATTAAT	8439
rs138913786	snp	C/T	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58595935	TCTAACTTATGAATT[C/T]GGGGAAATACAAGAC	8439
rs138913829	snp	A/T	0.000798403	0.0199641	intron-variant	NSMAF	GRCh38.p7	8:58643269	CTTGCCTTGTGTCCA[A/T]ATAACTACTATGTCA	8439
rs138928312	snp	G/T	0.0150606	0.0854603	intron-variant	NSMAF	GRCh38.p7	8:58655236	CTTGGCCTCCCAAAG[G/T]GCTGGGATTACAAGT	8439
rs138959726	snp	A/G	0.0123036	0.0774623	intron-variant	NSMAF	GRCh38.p7	8:58621148	TGTTCCCTTCTTTGC[A/G]TCCATTTGTACTCAA	8439
rs138976513	snp	A/T	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58610983	TGACAGATTTGATTG[A/T]CAGAGCCTCCCTGTA	8439
rs139025201	snp	C/G	0.00358779	0.0422022	intron-variant	NSMAF	GRCh38.p7	8:58657936	TACATGGAAATGCAA[C/G]TACAGGTTTCAAGGT	8439
rs139107276	in-del	-/AAC	0.00517822	0.0506191	intron-variant	NSMAF	GRCh38.p7	8:58629623	TATCCACACATTAAA[-/AAC]AACAACAACAACAAC	8439
rs139257218	snp	A/G	0.00199481	0.0315187	intron-variant	NSMAF	GRCh38.p7	8:58649745	CTCTTGCCATGTGAT[A/G]TACCTGCTCCCACTT	8439
rs139260915	snp	C/T	0.00478085	0.0486577	intron-variant	NSMAF	GRCh38.p7	8:58591788	AACTGTGCCCGGCCT[C/T]AAAACAACCTCTTAA	8439
rs139321192	snp	C/G	0.00119737	0.0244387	intron-variant	NSMAF	GRCh38.p7	8:58587472	AACCTAAAGAGTCAA[C/G]ACAAAGAAAAGAACT	8439
rs139325712	snp	C/T	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58588136	GGAATTCTAACAATT[C/T]TAGGTTCTTGCTTTC	8439
rs139327692	snp	C/T	0.0513262	0.151752	intron-variant	NSMAF	GRCh38.p7	8:58636085	ATCATTTTTCCAAGT[C/T]GTTAACTGCATTTAC	8439
rs139353415	snp	C/T	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58602831	ACTTTCCAAGTGTTC[C/T]ATAACAAATAATCAC	8439
rs139355331	snp	A/G	0.000181233	0.00951753	synonymous-codon	NSMAF	GRCh38.p7	8:58599778	GGGAAGCTCCACGTC[A/G]TCAACCATCTGTCCT	8439
rs139360502	snp	C/G	0.00874735	0.0655527	intron-variant	NSMAF	GRCh38.p7	8:58645697	GGCTACAATTAATAT[C/G]CCTACAAAGAAGAAG	8439
rs139378838	snp	G/T	0.00953873	0.0683987	upstream-variant-2KB	NSMAF	GRCh38.p7	8:58661541	TCGAGACCAGCCTGG[G/T]CAACAAAGCAAGACC	8439
rs139397159	snp	A/G	0.0154538	0.0865337	intron-variant	NSMAF	GRCh38.p7	8:58589908	TTAGAAAACAGTGCT[A/G]TGTCCTGGCAGGGAA	8439
rs139446771	snp	A/G	0.00874735	0.0655527	intron-variant	NSMAF	GRCh38.p7	8:58631031	TATGCTTAAGTGAAA[A/G]GTCCCAGGGAACCAG	8439
rs139458676	snp	A/G	0.00557542	0.0525036	intron-variant	NSMAF	GRCh38.p7	8:58636945	AATGCTTGATTCTTT[A/G]CCTTTATTTATCAAG	8439
rs139539085	in-del	-/C			intron-variant	NSMAF	GRCh38.p7	8:58645459	TTGGAAAAAACTAAA[-/C]CAGCCTCAGAGAAAA	8439
rs139562997	snp	A/G	0.00597247	0.0543191	intron-variant	NSMAF	GRCh38.p7	8:58629558	TATTTTGTACCTCTG[A/G]TTGGACTATTTTTCT	8439
rs139596316	snp	C/T	0.00874735	0.0655527	intron-variant	NSMAF	GRCh38.p7	8:58637102	TTAACATTTATGAAA[C/T]ATTTCAATCCATTGC	8439
rs139692322	snp	G/T	0.00517822	0.0506191	intron-variant	NSMAF	GRCh38.p7	8:58612963	CTGTCAACCTAGAAT[G/T]CTATATCCAAAAACA	8439
rs139716198	snp	A/G	0.00159617	0.0282053	intron-variant	NSMAF	GRCh38.p7	8:58616874	AATGAGTGAATTTAG[A/G]AGAGTCATAGTATAC	8439
rs139776887	snp	A/G/T	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58612363	TCTATGTGCCAGGAG[A/G/T]GTGATGTACCCTCAC	8439
rs139778478	in-del	-/A	0.0260105	0.111035	intron-variant	NSMAF	GRCh38.p7	8:58607918	AGTATCAGAAAGGGG[-/A]AAAAAAAATCACCAA	8439
rs139786186	snp	A/G	8.26849e-05	0.00642928	missense	NSMAF	GRCh38.p7	8:58623251	ATGTTCTAGCTAAAC[A/G]AGACTGCAAAATAGC	8439
rs139813149	snp	C/G	0.0283406	0.115616	upstream-variant-2KB	NSMAF	GRCh38.p7	8:58660030	GCATAAAAAGGGATG[C/G]TGGCCCATAAACCAC	8439
rs139863054	snp	C/T	0.000165082	0.0090837	synonymous-codon	NSMAF	GRCh38.p7	8:58635307	GAAAATGACATACTT[C/T]GTGAAGTGTCTATTG	8439
rs139896943	snp	C/T	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58622542	AGGATTACAGGTGCC[C/T]GCCACCATGCCTGGG	8439
rs139986925	snp	C/T	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58592536	CAGTAATATGAATTA[C/T]GAAAATCTAAATATG	8439
rs140016602	snp	C/T	0.00993419	0.0697739	intron-variant	NSMAF	GRCh38.p7	8:58658632	GATCTGTGGCTCTCA[C/T]AATCAAAACAGTGTG	8439
rs140016690	snp	G/T	0.00597247	0.0543191	intron-variant	NSMAF	GRCh38.p7	8:58618008	GAGTTCATGTCCTTT[G/T]CAGGGACATGGACGA	8439
rs140109769	snp	C/T	0.00279162	0.0372561	intron-variant	NSMAF	GRCh38.p7	8:58611825	TAACTTAAGTATAAC[C/T]GATTATAAAAGAAAA	8439
rs140141320	snp	A/G	0.00199481	0.0315187	intron-variant	NSMAF	GRCh38.p7	8:58608753	TGAGCCCCACCACCT[A/G]GTGGACACAATCACT	8439
rs140144207	snp	A/G	4.95503e-05	0.00497722	synonymous-codon	NSMAF	GRCh38.p7	8:58589488	TGCAGAATATAGCCT[A/G]TTGTCATGCCAACAG	8439
rs140163032	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	NSMAF	GRCh38.p7	8:58660551	TTGGGATATAACTCA[C/T]ATACCAAACAAGTCA	8439
rs140199734	snp	A/G	0.0185938	0.0946107	intron-variant	NSMAF	GRCh38.p7	8:58649079	TGAAAGCAGCCAAGT[A/G]GGCTGCACCCTTCAA	8439
rs140230826	snp	C/T	0.000798403	0.0199641	intron-variant	NSMAF	GRCh38.p7	8:58589374	CTTATAATATCTGTA[C/T]GTACATTTTAAGCTA	8439
rs140238260	snp	G/T	0.00676609	0.0577691	intron-variant	NSMAF	GRCh38.p7	8:58624873	ATTATTGTGTTGCTA[G/T]CTATTTCTCCCTTCA	8439
rs140271902	snp	A/C/T	0.0138799	0.0821421	intron-variant	NSMAF	GRCh38.p7	8:58605139	AATGTAATAAAAAAA[A/C/T]TTTGGGCTTGAACAT	8439
rs140279762	snp	A/G	6.58946e-05	0.0057396	missense	NSMAF	GRCh38.p7	8:58603282	GGTCGTTGCAGCTGC[A/G]GTCGGCCAGGTTGTT	8439
rs140301116	snp	C/T	0.00517822	0.0506191	intron-variant	NSMAF	GRCh38.p7	8:58619184	TGGAAATAAAATTAA[C/T]GCTATATAGTGAAGC	8439
rs140329740	in-del	-/AT	0.0596104	0.162024	intron-variant	NSMAF	GRCh38.p7	8:58641471	CCGATTTTTAAAAAC[-/AT]AGTGATAAATCTGCC	8439
rs140337580	snp	A/G			intron-variant	NSMAF	GRCh38.p7	8:58646149	TAATCTGTAACTTTT[A/G]TTGACCTGTCCTCCA	8439
rs140433357	snp	A/C	0.00438332	0.0466095	intron-variant	NSMAF	GRCh38.p7	8:58597691	GGATTGTCTAAACCT[A/C]ATTATAGACCTTCAG	8439
rs140433686	snp	G/T	0.0023933	0.0345097	intron-variant	NSMAF	GRCh38.p7	8:58639152	TAGCCAGAAATGGTG[G/T]CACGTGCTGTACGCC	8439
rs140438385	snp	C/T	0.00110309	0.0234591	missense	NSMAF	GRCh38.p7	8:58585736	GACTGCCAGATAAAA[C/T]GGAATTTCCATCCCA	8439
rs140503497	snp	C/T	0.00159617	0.0282053	intron-variant	NSMAF	GRCh38.p7	8:58656281	TTTGGGGATTACAGG[C/T]GTGAGCCCTGTGTCT	8439
rs140579437	snp	C/G	0.00268797	0.0365617	missense	NSMAF	GRCh38.p7	8:58599762	CACTGGAAGCCCAAG[C/G]GGGAAGCTCCACGTC	8439
rs140586276	snp	C/T	0.00159617	0.0282053	intron-variant	NSMAF	GRCh38.p7	8:58593806	CTAAATCAAATATCC[C/T]GAAGAAATATACACT	8439
rs140614316	in-del	-/A	0.0599851	0.162463	intron-variant	NSMAF	GRCh38.p7	8:58647595	GATAAATGAGTTCAC[-/A]ATCTGTTCACTCAAG	8439
rs140695181	in-del	-/TG			intron-variant	NSMAF	GRCh38.p7	8:58624174	AGCCTCCCGAGTAGC[-/TG]GGGCTAGAGGTGTGC	8439
rs140730866	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime	NSMAF	GRCh38.p7	8:58583597	AACTTACTAAGAACT[A/G]CTAATCCTTCTCCAG	8439
rs140758394	snp	C/T	0.000798403	0.0199641	intron-variant	NSMAF	GRCh38.p7	8:58627091	TTGTTTGAGGTTCCT[C/T]GTAGATTCTGGATGT	8439
rs140792558	snp	C/T	0.0475351	0.146656	intron-variant	NSMAF	GRCh38.p7	8:58588755	CATTGTTCCTTCTTT[C/T]CTTTGTCATCTTGGA	8439
rs140817904	snp	A/C	0.00119737	0.0244387	intron-variant	NSMAF	GRCh38.p7	8:58644111	ATGAGTTACAGGCAA[A/C]AGCTTTCATGAAAAG	8439
rs140848286	in-del	-/ATC			intron-variant	NSMAF	GRCh38.p7	8:58646044	AGACTCCGTCTCAAA[-/ATC]ATCATCATCATCATC	8439
rs140849154	in-del	-/C			intron-variant	NSMAF	GRCh38.p7	8:58626287	TTTTAGTAGAGACAG[-/C]GTTTCACAGTGTTAA	8439
rs140903039	snp	A/G	0.0130921	0.0798413	intron-variant	NSMAF	GRCh38.p7	8:58624299	TGATCCACCCGCCTC[A/G]GCCTCCCACAGTGCT	8439
rs140916412	snp	C/T	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58641835	ACACCTACATGGGGC[C/T]GTACCATTTTGCCCT	8439
rs140928325	snp	C/T	3.33072e-05	0.00408075	missense	NSMAF	GRCh38.p7	8:58590032	CCCATGAAGAAGTTA[C/T]GACAGTGGCATCTCC	8439
rs141143369	snp	A/G	0.00874735	0.0655527	intron-variant	NSMAF	GRCh38.p7	8:58640671	AAAATAATTTTCTGT[A/G]GCTAACTCCAACTTT	8439
rs141171976	snp	A/G	0.0023933	0.0345097	intron-variant	NSMAF	GRCh38.p7	8:58651763	GTTATCTAGCGCAGC[A/G]CTTCACAAAGGTTAG	8439
rs141212033	snp	C/T	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58645488	AAAGCCAGGTCTCTA[C/T]AACATCATCCCACAG	8439
rs141228279	snp	C/T	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58642665	TCTACAACCCCAGAA[C/T]TGGAACAAATGCTTT	8439
rs141283122	snp	C/T	0.00874735	0.0655527	intron-variant	NSMAF	GRCh38.p7	8:58639227	AGGCAGAGGTTGCAG[C/T]GAGCAGAGATCACGC	8439
rs141322725	snp	C/G	0.00199481	0.0315187	intron-variant	NSMAF	GRCh38.p7	8:58597128	GAAAGAGAACCACAT[C/G]AAAACATATATGGCC	8439
rs141379793	in-del	-/A	0.0402882	0.136092	intron-variant	NSMAF	GRCh38.p7	8:58652160	GCAGGATAGATGAAG[-/A]AAAAAAAAATCTATA	8439
rs141403706	snp	C/T	0.0126979	0.078662	intron-variant	NSMAF	GRCh38.p7	8:58614106	TCCTCACAATGACCA[C/T]TGCCTAACAACACGT	8439
rs141442542	snp	C/T	0.0130921	0.0798413	intron-variant	NSMAF	GRCh38.p7	8:58628200	GTAGAAGAATGAAAC[C/T]GGATCCTTATCTCTT	8439
rs141561489	snp	C/T	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58625277	GTCTGGAATTCTTGG[C/T]CTCTATAATCACATG	8439
rs141635262	snp	A/G	0.0126979	0.078662	intron-variant	NSMAF	GRCh38.p7	8:58614653	CCCCTTTGGAGAAGT[A/G]TGTATAAAAGTCAAG	8439
rs141749982	snp	C/T	0.000798403	0.0199641	intron-variant	NSMAF	GRCh38.p7	8:58632164	ACACCTCCCCAAACC[C/T]GTCAGATATTCAAAA	8439
rs141760460	snp	A/C	0.000798403	0.0199641	intron-variant	NSMAF	GRCh38.p7	8:58627584	CCAAGCTAAGAATCA[A/C]ATCAACAATTCCATT	8439
rs141793921	snp	A/G	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58630088	AATTTCTTCCCAATC[A/G]TGTGGTGCTGTGTGG	8439
rs141877327	snp	C/T	0.0115144	0.0749975	intron-variant	NSMAF	GRCh38.p7	8:58591628	AATAGCTGGGATTTT[C/T]TGACGTGCACACCAC	8439
rs141916240	in-del	-/AGAGT	0.0715223	0.175059	intron-variant	NSMAF	GRCh38.p7	8:58653131	ACACTGGTAGAGAGG[-/AGAGT]AAAGATAATGATTAG	8439
rs141959844	snp	G/T	0.000153988	0.00877328	stop-gained	NSMAF	GRCh38.p7	8:58609697	CACCATTTCTGCTTT[G/T]CATTCCATGTGCAGC	8439
rs141973474	snp	C/T	0.00119737	0.0244387	intron-variant	NSMAF	GRCh38.p7	8:58657888	AGCCTATCACGTTGT[C/T]GTCTAATCAATGAAT	8439
rs142087727	snp	A/G	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58588915	GACCATTCATCCCAC[A/G]ATGGAATACACAGTA	8439
rs142092969	snp	A/G			intron-variant	NSMAF	GRCh38.p7	8:58631999	TGGTCCTTACATAGT[A/G]TATTAATAACTATGT	8439
rs142123842	snp	G/T	0.0023933	0.0345097	intron-variant	NSMAF	GRCh38.p7	8:58616582	CTCTCAGTAAACTAG[G/T]AACAGAAAGGAATAT	8439
rs142165848	snp	A/G	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58613475	ACACAAAGTGCTACA[A/G]CTAAAAAGTCAATAG	8439
rs142178018	snp	C/T	0.0150606	0.0854603	intron-variant	NSMAF	GRCh38.p7	8:58654433	CGCATGCCTGTAATC[C/T]CAGCTACTTGGGAGG	8439
rs142178137	snp	A/C	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58610784	GTGCAAAACAAGGGA[A/C]ATCTCCCACAGTTCA	8439
rs142189452	snp	A/G	0.00199481	0.0315187	intron-variant	NSMAF	GRCh38.p7	8:58611871	AGAGGAAATGGAGAA[A/G]AGAATGGCTGAGAAC	8439
rs142189658	snp	A/G	0.00517822	0.0506191	intron-variant	NSMAF	GRCh38.p7	8:58655252	GCTGGGATTACAAGT[A/G]TAAGCCATGGCACCT	8439
rs142191042	snp	A/G	0.0103295	0.0711199	intron-variant	NSMAF	GRCh38.p7	8:58585266	GAGGTAGGAGTCAGC[A/G]GTAGAAAGAAGCCTT	8439
rs142203067	snp	A/T	0.0146672	0.084371	intron-variant	NSMAF	GRCh38.p7	8:58653831	AAAATTTTTAATGAA[A/T]ATTATATAGCTTACA	8439
rs142243518	snp	A/C	0.00874735	0.0655527	intron-variant	NSMAF	GRCh38.p7	8:58651537	ATCCATAAAGCCAGT[A/C]AATTCTATTTTCAAG	8439
rs142278918	snp	C/T	0.000247168	0.0111141	missense	NSMAF	GRCh38.p7	8:58602120	TGAGATCCCGGAAGG[C/T]TCCTGGATTTGACAA	8439
rs142293482	snp	A/G	0.000313203	0.0125101	synonymous-codon	NSMAF	GRCh38.p7	8:58609655	GTCCGTGATGCACAC[A/G]TGTCCAGGATTAGTC	8439
rs142450621	snp	A/G	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58638961	TATTAAAAGACAGGC[A/G]GAGGACCTGAATAGA	8439
rs142454070	in-del	-/TATA			intron-variant	NSMAF	GRCh38.p7	8:58604565	ATATATAATATATAT[-/TATA]ATATAAACCTACTTT	8439
rs142532753	snp	C/T	0.000798403	0.0199641	intron-variant	NSMAF	GRCh38.p7	8:58593362	GCTACAGATCATAAA[C/T]AATGATAACAGAATC	8439
rs142537914	snp	A/G	0.0103295	0.0711199	intron-variant	NSMAF	GRCh38.p7	8:58596404	CTCCACAGAGTGTCA[A/G]CCTCCTTCTGGAAGC	8439
rs142542935	snp	A/G	0.000494454	0.0157157	missense	NSMAF	GRCh38.p7	8:58589537	TCATGTCCCATTAAC[A/G]TGTCCTGGCGTCTTC	8439
rs142545036	snp	A/G	0.0023933	0.0345097	intron-variant	NSMAF	GRCh38.p7	8:58638828	AATTAACAAAGTCAA[A/G]AGACAACCTACGGAA	8439
rs142605608	snp	C/T	0.0023933	0.0345097	intron-variant	NSMAF	GRCh38.p7	8:58592250	TCTCTCCTTGATGTC[C/T]AGTGGTTAGGATTTG	8439
rs142618981	snp	A/G	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58636209	ATGGCCTAGCTCTAC[A/G]ATTGTCAATATGTGG	8439
rs142642956	snp	A/G	0.000400982	0.0141538	intron-variant	NSMAF	GRCh38.p7	8:58623805	AGGGGAAGATATCAA[A/G]ATACAGGAAGAGAAG	8439
rs142652236	snp	G/T	0.12932	0.218944	upstream-variant-2KB, utr-variant-5-prime	NSMAF	GRCh38.p7	8:58659781	GCGGCGCCGCTGGGC[G/T]GCCGAGAGCCCGACG	8439
rs142686417	snp	C/T	0.00318978	0.0398085	intron-variant	NSMAF	GRCh38.p7	8:58611031	TAAGAGGTGGCTTGA[C/T]CACTTCTGGAGGTAA	8439
rs142821507	snp	C/T	0.00398564	0.0444627	intron-variant	NSMAF	GRCh38.p7	8:58653956	AGGCTAGTAATACAT[C/T]TTGGGTAAAGTCAAT	8439
rs142844478	snp	A/C/T	8.40394e-05	0.00648181	missense	NSMAF	GRCh38.p7	8:58590008	GCACAGATACATACA[A/C/T]ATTATTATCCCATGA	8439
rs142915707	snp	G/T	0.00597247	0.0543191	intron-variant	NSMAF	GRCh38.p7	8:58608370	GAAGAAAATTGTCTT[G/T]CTTTTCTATAATTTT	8439
rs142942697	snp	C/T	0.00914312	0.0669923	intron-variant	NSMAF	GRCh38.p7	8:58653106	AGCAGTTAAGTGTTC[C/T]AAGGTTCTTACACTG	8439
rs142982194	snp	C/G	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58612386	ACCCTCACTCCACAG[C/G]GACAGAAGCTCCTGC	8439
rs143006088	snp	A/G	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58648374	AACTCTGGGAAATTT[A/G]TAGCCCGGCCATGTG	8439
rs143043635	snp	C/G	0.00478085	0.0486577	intron-variant	NSMAF	GRCh38.p7	8:58587204	CTTGACCATCCCAGA[C/G]AGCTGGTCACTGTCC	8439
rs143050199	snp	C/T	0.00755907	0.0610114	intron-variant	NSMAF	GRCh38.p7	8:58657937	ACATGGAAATGCAAG[C/T]ACAGGTTTCAAGGTT	8439
rs143061129	snp	A/G	0.000148425	0.0086134	synonymous-codon	NSMAF	GRCh38.p7	8:58623745	ATCTTCCACTTTCCC[A/G]GGAACATCCAATTCA	8439
rs143061385	in-del	-/TTTTCT	0.0596104	0.162024	intron-variant	NSMAF	GRCh38.p7	8:58650443	TATTTGCTAGCCTGA[-/TTTTCT]TTTTCTTTTTTAGCT	8439
rs143063886	in-del	-/TTG	0.079617	0.182947	intron-variant	NSMAF	GRCh38.p7	8:58595114	TTAGAAGCATAATTA[-/TTG]TTTTTAAAATTCATG	8439
rs143199390	snp	C/G	0.00676609	0.0577691	upstream-variant-2KB	NSMAF	GRCh38.p7	8:58660261	GAAATTCTGGCTGAA[C/G]CAACCTAACAGGAGT	8439
rs143256721	snp	A/G	0.00358779	0.0422022	intron-variant	NSMAF	GRCh38.p7	8:58628065	GGAACAGAACAGACA[A/G]CCCAGAAATAAAGCC	8439
rs143359529	snp	A/C	0.0178098	0.0926698	intron-variant	NSMAF	GRCh38.p7	8:58625088	GAGTAAAACAGATTG[A/C]CCTCCCCAATGTGGG	8439
rs143400607	snp	A/C/T	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58646719	TCAAACTACATTTTA[A/C/T]GGAGTAAAAGAGTCC	8439
rs143437399	snp	A/C	0.00318978	0.0398085	intron-variant	NSMAF	GRCh38.p7	8:58626116	TTTTTTTTTTTTGAG[A/C]TGGAGTCTCACTGTG	8439
rs143464405	snp	A/T	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58654794	CTATGACTCTTCCTC[A/T]GAAGGAAACATATCT	8439
rs143464800	snp	A/G	0.0599851	0.162463	intron-variant	NSMAF	GRCh38.p7	8:58644979	GGGGTGGGGAGCTAG[A/G]GGAGGGATAGCATTA	8439
rs143492573	snp	C/T	0.000148249	0.00860829	missense	NSMAF	GRCh38.p7	8:58597458	TTTGGGGTGATCCTT[C/T]GAGGATGTGGTGTCA	8439
rs143505109	snp	A/G	0.00636936	0.0560724	intron-variant	NSMAF	GRCh38.p7	8:58624423	AACTTCCCTGTTTAT[A/G]CTGCTTTTGCTGCAT	8439
rs143612297	in-del	-/T			intron-variant	NSMAF	GRCh38.p7	8:58656024	CCTGCTATCTAAATC[-/T]TTTTTTTGTTTGTTT	8439
rs143614595	snp	A/C	0.00438332	0.0466095	intron-variant	NSMAF	GRCh38.p7	8:58614154	GCGGGAAATTAAAGA[A/C]AAATAAAATTAAAAA	8439
rs143673373	snp	C/T	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58590808	GTATTATTGTATGGG[C/T]GTGTATAAAACAAAC	8439
rs143700391	snp	C/T	0.00279162	0.0372561	intron-variant	NSMAF	GRCh38.p7	8:58606391	TTCTTCAAACATAAA[C/T]GTCTAGCTTTCTTTC	8439
rs143706617	snp	C/T	0.00874735	0.0655527	intron-variant	NSMAF	GRCh38.p7	8:58634124	CAGAATTATTAATAA[C/T]GATGTTTGGTCCCCA	8439
rs143723291	snp	A/G	0.0599851	0.162463	intron-variant	NSMAF	GRCh38.p7	8:58646016	ACTGCACTCCAGCCT[A/G]GGCAACAAGAGCGAG	8439
rs143744312	snp	A/C/T	0.00119737	0.0244387	intron-variant	NSMAF	GRCh38.p7	8:58657768	ATATAAAACACATGG[A/C/T]GCCAACTTTTTCAGA	8439
rs143780760	snp	C/T	0.00398564	0.0444627	intron-variant	NSMAF	GRCh38.p7	8:58586215	ATGAGTTCATTTTTA[C/T]CTTAAATTAATTTCT	8439
rs143795707	snp	C/T	0.0107246	0.0724382	intron-variant	NSMAF	GRCh38.p7	8:58598570	CATAGGAATTGAGGC[C/T]ACTGTTCTATCACAC	8439
rs143811464	snp	A/G	0.000511378	0.0159821	missense	NSMAF	GRCh38.p7	8:58609680	TTAGTCACCAGAGGC[A/G]TCACCATTTCTGCTT	8439
rs143812039	snp	C/G	0.00199481	0.0315187	utr-variant-3-prime	NSMAF	GRCh38.p7	8:58583565	TAATGAAATACAAAC[C/G]GTTCCTATACACAGT	8439
rs143815884	snp	A/G	0.0023933	0.0345097	intron-variant	NSMAF	GRCh38.p7	8:58627975	GCATCACATTATTCA[A/G]CTTCAAAATATACTA	8439
rs143817244	snp	A/G	9.90737e-05	0.00703754	synonymous-codon	NSMAF	GRCh38.p7	8:58589491	AGAATATAGCCTGTT[A/G]TCATGCCAACAGATC	8439
rs143857347	snp	C/G	0.00438332	0.0466095	intron-variant	NSMAF	GRCh38.p7	8:58608923	GTTAGGATTTCTGTT[C/G]TTTTAATGGATCATG	8439
rs143879961	snp	A/C/T	0.0142982	0.0835538	intron-variant	NSMAF	GRCh38.p7	8:58625519	TTTCTGATAAATTGA[A/C/T]CCTTTTATCATTACA	8439
rs143916762	snp	A/G	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58603650	TAAACAAATACAAAA[A/G]TGTAGCGCAAATATA	8439
rs143955175	snp	C/T	0.00716266	0.059414	intron-variant	NSMAF	GRCh38.p7	8:58611565	TGAAAAGACAGAGTT[C/T]CAGCAGAGAAATAGA	8439
rs143992092	in-del	-/T	0.00279162	0.0372561	intron-variant	NSMAF	GRCh38.p7	8:58648543	AAGTCATTTCAGAAG[-/T]TTTTCAGGATGTCCC	8439
rs144003915	snp	A/T	0.00874735	0.0655527	intron-variant	NSMAF	GRCh38.p7	8:58626600	TATAGGACTTTTTCC[A/T]CTTGTTGGTTGATGG	8439
rs144005823	snp	A/G	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58625706	TTGCAGATGGCATAT[A/G]GTTTTAGATCTTATT	8439
rs144059643	snp	A/G	6.59326e-05	0.00574125	synonymous-codon	NSMAF	GRCh38.p7	8:58586564	GCCTTCTTTGGTGCC[A/G]GAAACTAACAGTGTG	8439
rs144123853	snp	C/T	0.00398564	0.0444627	intron-variant	NSMAF	GRCh38.p7	8:58588160	TGCTTTCTTTTACAC[C/T]AACACAAAATAGAAA	8439
rs144140694	snp	C/T	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58639810	TGGAATATTATTCAG[C/T]CTCAAAAAAGGAAAT	8439
rs144156948	snp	C/T	0.000642605	0.0179134	intron-variant	NSMAF	GRCh38.p7	8:58585874	CTGTAAATGTCTTCG[C/T]CCCCAGTAACTCACA	8439
rs144157766	snp	C/T	0.00119737	0.0244387	intron-variant	NSMAF	GRCh38.p7	8:58631106	ACTTACAAATTATTA[C/T]TGAGTTCTCAAATAA	8439
rs144205198	in-del	-/TAA			intron-variant	NSMAF	GRCh38.p7	8:58591941	CTGCACAGTATAACT[-/TAA]TAATTCAACCCAATT	8439
rs144218057	snp	C/T	0.0197687	0.0974348	intron-variant	NSMAF	GRCh38.p7	8:58655885	GCACTCCAGCCTGGG[C/T]GAGAGTGAGACTCCG	8439
rs144256965	snp	G/T	0.000611151	0.01747	missense	NSMAF	GRCh38.p7	8:58601306	AACATTCTATCTGCA[G/T]TATCAAATCTTCCAT	8439
rs144276701	snp	A/T	4.94531e-05	0.00497234	missense	NSMAF	GRCh38.p7	8:58599859	ATCATCACCATAGAA[A/T]TCTGGAATTAACTGA	8439
rs144319758	snp	A/C	0.0107246	0.0724382	intron-variant	NSMAF	GRCh38.p7	8:58597701	AACCTCATTATAGAC[A/C]TTCAGAATATTTTCT	8439
rs144463073	snp	C/T	0.0599851	0.162463	intron-variant	NSMAF	GRCh38.p7	8:58645766	AAATAATAGGCCAGG[C/T]GCAGCGGCTCACACC	8439
rs144515120	snp	A/G	0.000214127	0.0103449	synonymous-codon	NSMAF	GRCh38.p7	8:58603271	GTACTGGGAGAGGTC[A/G]TTGCAGCTGCGGTCG	8439
rs144527895	snp	C/T	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58587777	TGCATTCAAGAAAAA[C/T]TCCTATGCTCAATTT	8439
rs144534227	snp	C/T	0.00582728	0.0536627	upstream-variant-2KB, intron-variant	NSMAF	GRCh38.p7	8:58659427	TTTCCGCCACAGCCC[C/T]CAGCCCAGGCCCTGG	8439
rs144552140	snp	G/T	0.000153988	0.00877328	missense	NSMAF	GRCh38.p7	8:58643017	TTGTGCAAAATGTGA[G/T]TGGCTCTATGCTGTT	8439
rs144600575	snp	C/T	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58600336	ACACTGAAAGATTAG[C/T]ACCACTGGTAGGGCG	8439
rs144608080	snp	A/G	0.00412994	0.0452539	missense	NSMAF	GRCh38.p7	8:58607807	TTTTGTAGATGCGGC[A/G]GACATCTTGGAGTGT	8439
rs144620540	snp	A/G	0.00358779	0.0422022	intron-variant	NSMAF	GRCh38.p7	8:58620461	TTGGGGCCATGTTAA[A/G]GTGTTTAGGCTTTAT	8439
rs144634636	snp	C/T	0.00028131	0.0118565	synonymous-codon	NSMAF	GRCh38.p7	8:58601449	AAGAATCTTACCAAT[C/T]CTAACAAGATAAAAA	8439
rs144667907	snp	A/G	0.0023933	0.0345097	intron-variant	NSMAF	GRCh38.p7	8:58657569	ATTCCTCTGTTTCAG[A/G]ATGAATTCTAAGATT	8439
rs144678337	snp	C/T	0.0150606	0.0854603	intron-variant	NSMAF	GRCh38.p7	8:58656007	CAATATGGTTCCTGC[C/T]ATCTAAATCTTTTTT	8439
rs144679672	snp	C/T	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58655154	TATTTATTTTTTAAA[C/T]AGAGAAAAGGTCTCC	8439
rs144693853	snp	A/G			utr-variant-3-prime	NSMAF	GRCh38.p7	8:58583907	TTTCCTAACACAGCC[A/G]CATTTTATCTGCCCT	8439
rs144708345	in-del	-/AAATAATAAAAT	0.216472	0.247742	intron-variant	NSMAF	GRCh38.p7	8:58606052	ATAAATTCAAAAAGA[-/AAATAATAAAAT]AAATAATAAAATAAA	8439
rs144737228	snp	A/T	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58585043	GGGATAACAAGAGAC[A/T]CTAGAAGAATTAAAA	8439
rs144741992	snp	G/T	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58654255	CTTGCCAAGTGCTTT[G/T]TATAAAATAAATATA	8439
rs144846583	snp	A/T	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58653850	ATATAGCTTACATAC[A/T]CAAAATCCATTTATG	8439
rs144877578	snp	C/T	9.30501e-05	0.00682029	missense	NSMAF	GRCh38.p7	8:58631527	GGTGCAACAACATTA[C/T]GTTCTTTAATGAAAT	8439
rs145049734	snp	C/G/T	0.0180909	0.0933734	intron-variant	NSMAF	GRCh38.p7	8:58643086	AATCTGGATTTGGGG[C/G/T]GAAAAAACAACTTTC	8439
rs145050534	snp	C/T	0.00636936	0.0560724	intron-variant	NSMAF	GRCh38.p7	8:58595781	CACCCTGTCACAATA[C/T]AACTGCTTTGAAATG	8439
rs145137115	snp	A/G	0.00557542	0.0525036	intron-variant	NSMAF	GRCh38.p7	8:58620022	AGATACAGACGAATC[A/G]CCTAAATCTCCTTGA	8439
rs145150387	snp	A/C	0.00055788	0.0166922	intron-variant	NSMAF	GRCh38.p7	8:58637373	TGGTGCTGATTGCAA[A/C]TGAGTTATTTCTAGG	8439
rs145238522	snp	C/T	0.0023933	0.0345097	intron-variant	NSMAF	GRCh38.p7	8:58610241	TCTGTGAATTTACTG[C/T]AGAAAACCTCTGAAA	8439
rs145287691	snp	C/T	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58649946	GTGGTTTATAAATAA[C/T]CTGTCTGATCTAGAA	8439
rs145302601	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	NSMAF	GRCh38.p7	8:58661024	TTTTTATGGACCTAT[A/G]TTTCCATTTCTGTTG	8439
rs145313280	snp	A/G	0.000307953	0.0124049	synonymous-codon	NSMAF	GRCh38.p7	8:58590071	GTAAACAAGACGATA[A/G]AGCCTGAAATACAAA	8439
rs145334211	snp	A/C	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58624892	TTTCTCCCTTCAGTT[A/C]TATCAATGTTCGCTT	8439
rs145346621	snp	A/G	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58620608	GTGTATGGCTGTAAA[A/G]GACTATTTGTGTCTT	8439
rs145400140	snp	C/T	0.00874735	0.0655527	intron-variant	NSMAF	GRCh38.p7	8:58623563	GGCTTCTTCCTAATA[C/T]ATAGTTTTTAAACTC	8439
rs145443754	snp	C/T	0.00438332	0.0466095	intron-variant	NSMAF	GRCh38.p7	8:58592763	ACGATGGTGGGTGCC[C/T]GTGAACCCAGCTACT	8439
rs145506455	in-del	-/TATATATGTATGTATGTATG/TATATATGTATGTATGTATGTATG	0.278399	0.248382	intron-variant	NSMAF	GRCh38.p7	8:58625394	ATATATGTATATGCA[lengthTooLong]TATGTATGTATGTAT	8439
rs145605691	snp	C/G	1.64749e-05	0.00287005	missense	NSMAF	GRCh38.p7	8:58643023	AAAATGTGATTGGCT[C/G]TATGCTGTTCAAAGT	8439
rs145670976	snp	A/G	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58604009	ATCTTAGATAAATGC[A/G]GCAATGAGAACTTCC	8439
rs145717567	snp	A/T	0.0134861	0.0810011	intron-variant	NSMAF	GRCh38.p7	8:58600085	TAGCAGCATTTCCTA[A/T]GCACTTGGGGGCTGT	8439
rs145730575	snp	A/G	0.00159617	0.0282053	intron-variant	NSMAF	GRCh38.p7	8:58646720	CAAACTACATTTTAC[A/G]GAGTAAAAGAGTCCA	8439
rs145789659	snp	C/T	0.00676609	0.0577691	intron-variant	NSMAF	GRCh38.p7	8:58627367	AAGTCCTAGCCACAG[C/T]AATCAGACAGAAAAG	8439
rs145857425	snp	C/T	0.00874735	0.0655527	intron-variant	NSMAF	GRCh38.p7	8:58641849	CTGTACCATTTTGCC[C/T]TAATAGTTACTTTAA	8439
rs145930714	snp	A/G	1.65425e-05	0.00287593	stop-gained	NSMAF	GRCh38.p7	8:58597546	TCTCATCAGGATCCT[A/G]GATGCTTTGGGACAG	8439
rs146010335	snp	C/G	0.0107246	0.0724382	intron-variant	NSMAF	GRCh38.p7	8:58596564	GCCCAGCGCAGAACA[C/G]ATACCCTGTAAATGT	8439
rs146013099	snp	C/T	0.00318978	0.0398085	intron-variant	NSMAF	GRCh38.p7	8:58613837	ATATCGGTGTGCCTC[C/T]CTAATCACAAAATCT	8439
rs146029974	snp	A/C	0.00636936	0.0560724	intron-variant	NSMAF	GRCh38.p7	8:58592278	TTGGTGCTCTCACTG[A/C]AGCAGCCTGGGTTCA	8439
rs146075702	in-del	-/TA			intron-variant	NSMAF	GRCh38.p7	8:58606215	ACATATACGTTTGCG[-/TA]TATATATATATGTTG	8439
rs146112363	snp	G/T	0.0283406	0.115616	intron-variant	NSMAF	GRCh38.p7	8:58653286	TCCAAAGGAAGAAGG[G/T]AAGGAAGGCAAAATA	8439
rs146130275	snp	A/G	0.00517822	0.0506191	intron-variant	NSMAF	GRCh38.p7	8:58610872	GAGATCCCAAGTCCT[A/G]TGGAAGAGAAAGTCT	8439
rs146147055	snp	A/G	0.00199481	0.0315187	intron-variant	NSMAF	GRCh38.p7	8:58648793	AGAATGCAAGCATGA[A/G]GGAGCCTTGGCAGCT	8439
rs146159106	snp	A/C	0.00874735	0.0655527	intron-variant	NSMAF	GRCh38.p7	8:58651556	TCTATTTTCAAGTCC[A/C]AGCAATTTATGAGAA	8439
rs146232790	snp	A/C/G	0.00178266	0.0298023	intron-variant	NSMAF	GRCh38.p7	8:58635273	CAGCTTTTTGGTTGA[A/C/G]GTAAAATTAAACAGT	8439
rs146265969	snp	A/G	0.00119737	0.0244387	intron-variant	NSMAF	GRCh38.p7	8:58630221	TTTCTCACAAAGGGA[A/G]TTTGTCCATGTGTTG	8439
rs146351476	snp	A/G	9.89201e-05	0.00703209	synonymous-codon	NSMAF	GRCh38.p7	8:58589518	GATCTTACTAACAGC[A/G]TCATCATGTCCCATT	8439
rs146351652	snp	A/G	0.00517822	0.0506191	intron-variant	NSMAF	GRCh38.p7	8:58616832	CATGAAAACTCCATG[A/G]AATCTAGCAAAAAAC	8439
rs146386677	in-del	-/TAAA	1.65633e-05	0.00287774	utr-variant-3-prime	NSMAF	GRCh38.p7	8:58584065	GGTTTAAAAATGCAT[-/TAAA]TAGAGTTCAATTTAA	8439
rs146409525	snp	A/C	0.00557542	0.0525036	intron-variant	NSMAF	GRCh38.p7	8:58657464	AATCCAATCCATTTG[A/C]TAATTTGTGTTTATT	8439
rs146413959	snp	C/T	0.000798403	0.0199641	intron-variant	NSMAF	GRCh38.p7	8:58586056	AGAATGTGGTTTACA[C/T]TATTCTGGATTTTAT	8439
rs146520291	snp	A/C	0.380138	0.213458	intron-variant	NSMAF	GRCh38.p7	8:58588724	TGCACGTGGCCGCGG[A/C]CCTTTTTGGCACGAC	8439
rs146530407	snp	C/T	0.0379877	0.132479	upstream-variant-2KB, utr-variant-5-prime	NSMAF	GRCh38.p7	8:58659797	GCCGAGAGCCCGACG[C/T]GGCGTCCCGGCCGCG	8439
rs146533360	snp	C/T	0.00159617	0.0282053	intron-variant	NSMAF	GRCh38.p7	8:58642555	TTTATAACATTGTCA[C/T]CCGAATAATTGAGAG	8439
rs146594730	in-del	-/AA	0.0475351	0.146656	intron-variant	NSMAF	GRCh38.p7	8:58585565	GGGTGTTTTTTGCCC[-/AA]AAAGAGTATGTTCCC	8439
rs146647649	snp	C/G	0.0225045	0.103662	intron-variant	NSMAF	GRCh38.p7	8:58645788	GCTCACACCTGTAAT[C/G]CCAGCACTTCGGGAG	8439
rs146669277	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	NSMAF	GRCh38.p7	8:58660410	CATTTACAAGGAAGT[G/T]CACACAAGGACCTGG	8439
rs146767847	snp	A/C	0.0107246	0.0724382	intron-variant	NSMAF	GRCh38.p7	8:58626136	GTCTCACTGTGTCAC[A/C]CAGGCTGGATGGAGT	8439
rs146901191	snp	A/G	0.000131889	0.00811956	missense	NSMAF	GRCh38.p7	8:58589547	TTAACGTGTCCTGGC[A/G]TCTTCCAAATGCTAT	8439
rs146992366	snp	C/T	0.00279162	0.0372561	intron-variant	NSMAF	GRCh38.p7	8:58651005	TTTCCAATTGTGTTC[C/T]CTGGGATTTTTTCCT	8439
rs147008504	snp	A/G	0.00159617	0.0282053	intron-variant	NSMAF	GRCh38.p7	8:58646655	CTTTAAAATTTTTCT[A/G]TGTAAAAATTATTAT	8439
rs147027400	snp	A/G	0.00438332	0.0466095	upstream-variant-2KB	NSMAF	GRCh38.p7	8:58661690	CTGTGAGCCATGATC[A/G]TACCACTGCACCCCA	8439
rs147111951	snp	A/C	0.00478085	0.0486577	intron-variant	NSMAF	GRCh38.p7	8:58627610	CCATTCCTTTTATAA[A/C]AGCTGCAAAAAAAAT	8439
rs147176369	snp	G/T	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58641722	TGTGCATATGTCCAT[G/T]TATATAACTGCCAGT	8439
rs147219674	snp	C/G	0.0119091	0.0762411	intron-variant	NSMAF	GRCh38.p7	8:58606398	AACATAAATGTCTAG[C/G]TTTCTTTCATAAGTT	8439
rs147254735	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime	NSMAF	GRCh38.p7	8:58583566	AATGAAATACAAACC[A/G]TTCCTATACACAGTA	8439
rs147265710	snp	C/G	0.0126979	0.078662	intron-variant	NSMAF	GRCh38.p7	8:58614513	AGATAATGGACATCT[C/G]GGTTGCATAGCAATG	8439
rs147272494	snp	C/T	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58625599	CTGATATAAGTATGG[C/T]TAGCTCTGTTGTTTG	8439
rs147275100	snp	G/T			intron-variant	NSMAF	GRCh38.p7	8:58623569	TTCCTAATATATAGT[G/T]TTTAAACTCAACATT	8439
rs147332065	snp	C/G	5.14999e-05	0.00507418	intron-variant	NSMAF	GRCh38.p7	8:58586638	ACATTGATACATATT[C/G]CATTAGATTTATGGT	8439
rs147344169	snp	C/T	0.00119737	0.0244387	intron-variant	NSMAF	GRCh38.p7	8:58641059	CCCAAGTAGCTGGGA[C/T]TACAAGGGTGCACCA	8439
rs147432706	snp	A/G	0.00874735	0.0655527	intron-variant	NSMAF	GRCh38.p7	8:58644820	GTCCTTTGCAGCGAC[A/G]TGGATGAAGCTGGAA	8439
rs147448493	snp	A/G	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58621237	ATTTGCTCCAGCGCC[A/G]TCCGTGGCCTCCAGC	8439
rs147469873	snp	A/C	3.70741e-05	0.00430531	missense	NSMAF	GRCh38.p7	8:58631521	TTATATGGTGCAACA[A/C]CATTATGTTCTTTAA	8439
rs147493861	snp	C/G	0.0832709	0.186283	intron-variant	NSMAF	GRCh38.p7	8:58656121	CCTCCCAGGTTCAAG[C/G]AATTCTCCTGCCTCA	8439
rs147537159	snp	C/T	0.00874735	0.0655527	intron-variant	NSMAF	GRCh38.p7	8:58625423	ATGTATGTATATATA[C/T]GTGTGAATGTATGTA	8439
rs147582418	snp	C/T	0.00269443	0.0366054	intron-variant	NSMAF	GRCh38.p7	8:58597575	AGAACACAAATAATG[C/T]AGTGAACCACTAGGT	8439
rs147591576	snp	A/G	0.00119737	0.0244387	intron-variant	NSMAF	GRCh38.p7	8:58593293	TTCTATGCTTTGTGG[A/G]AAATTTTTTTATATA	8439
rs147602341	snp	A/G	0.00993419	0.0697739	intron-variant	NSMAF	GRCh38.p7	8:58654321	AAAGTTGGGCCGGGC[A/G]TGGTGGCTCACCTGA	8439
rs147618593	snp	A/G	0.00874735	0.0655527	intron-variant	NSMAF	GRCh38.p7	8:58651228	CTCATTTTATTATCC[A/G]TGTTCTACACATTTG	8439
rs147647770	snp	C/T	4.94907e-05	0.00497422	missense	NSMAF	GRCh38.p7	8:58594264	ACTGAAGATCCATTG[C/T]GAGAGACCGTGATTC	8439
rs147657608	in-del	-/ATAT			intron-variant	NSMAF	GRCh38.p7	8:58604560	TAGATATATATAATA[-/ATAT]TATATATATAAACCT	8439
rs147712910	snp	C/T	0.0185938	0.0946107	intron-variant	NSMAF	GRCh38.p7	8:58638057	AAACAATCTGTTTTG[C/T]TTCATTTTAAGAAAT	8439
rs147741715	snp	C/T	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58632400	GTCACATGAAGTGCA[C/T]AAGATCTCCACGTCA	8439
rs147816862	snp	C/T	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58618419	TTATTATATATGAGA[C/T]ATATTATGGAATTAT	8439
rs147846446	snp	A/T	0.00199481	0.0315187	intron-variant	NSMAF	GRCh38.p7	8:58613847	GCCTCCCTAATCACA[A/T]AATCTGAAATCTGAA	8439
rs147866066	snp	C/T	6.62087e-05	0.00575326	missense	NSMAF	GRCh38.p7	8:58601498	GAGTAGTGACTCCCA[C/T]ACATGAACTTTGGTT	8439
rs147897385	snp	A/G	0.00597247	0.0543191	intron-variant	NSMAF	GRCh38.p7	8:58617647	AATGGCAATCATTAA[A/G]AAGTCAGGAAACAAC	8439
rs147914201	snp	A/G	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58613472	ATAACACAAAGTGCT[A/G]CAGCTAAAAAGTCAA	8439
rs147922619	snp	C/T	0.00299725	0.0385959	intron-variant	NSMAF	GRCh38.p7	8:58597953	GCTATTTCAATGTAA[C/T]ATACACTGTTTAGAA	8439
rs147951951	snp	C/T	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58593724	CATATCAATGACACA[C/T]TGCAAGGGTTTTTAT	8439
rs147985912	snp	C/T	0.00953873	0.0683987	intron-variant	NSMAF	GRCh38.p7	8:58654959	CTTGTCTCAGTCTCC[C/T]GAGTAGCTGGGATTA	8439
rs147990005	snp	A/T	1.64738e-05	0.00286995	missense	NSMAF	GRCh38.p7	8:58597475	AGGATGTGGTGTCAC[A/T]AATAGTTGTTTTGGT	8439
rs148067365	snp	C/T	0.0119091	0.0762411	intron-variant	NSMAF	GRCh38.p7	8:58600352	ACCACTGGTAGGGCG[C/T]GGTGGCTCACACCTG	8439
rs148145587	snp	C/T	0.0123036	0.0774623	intron-variant	NSMAF	GRCh38.p7	8:58657869	GTTCTCTCTGAACAC[C/T]GCCAGCCTATCACGT	8439
rs148148194	snp	C/T	3.30437e-05	0.00406457	missense	NSMAF	GRCh38.p7	8:58609695	GTCACCATTTCTGCT[C/T]TGCATTCCATGTGCA	8439
rs148182874	snp	C/T	0.00119737	0.0244387	intron-variant	NSMAF	GRCh38.p7	8:58651670	CAGCCTTTTTATATG[C/T]ACTATCAAGAAGTTA	8439
rs148303650	snp	C/T	0.00119737	0.0244387	intron-variant	NSMAF	GRCh38.p7	8:58628090	AAAGCCAAATACTTA[C/T]AGCCAACTGATCTTT	8439
rs148355171	snp	C/G/T	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58625230	TTGCATTCAGACTCA[C/G/T]ACTAAACGCTATACC	8439
rs148436988	snp	C/T	0.00676609	0.0577691	intron-variant	NSMAF	GRCh38.p7	8:58608186	AACTGGCATAAATAA[C/T]CTCTCAGGAATCTTG	8439
rs148453600	snp	A/G	0.000798403	0.0199641	intron-variant	NSMAF	GRCh38.p7	8:58623613	CTACATATTTAGAAA[A/G]CAGATGATGATTTGG	8439
rs148456704	snp	C/G	0.00626517	0.0556177	upstream-variant-2KB, missense	NSMAF	GRCh38.p7	8:58659589	TCTCCTTGGAGTAGA[C/G]CTGCAGCTGCTGCTC	8439
rs148557673	snp	A/G	0.00279162	0.0372561	intron-variant	NSMAF	GRCh38.p7	8:58648026	GAGACTGGTTAAATG[A/G]TTGTGACCAAAATAC	8439
rs148646550	snp	A/T	0.00993419	0.0697739	intron-variant	NSMAF	GRCh38.p7	8:58645367	AAAACATGGAATAGA[A/T]GAACACTAGTTTGCT	8439
rs148661666	snp	A/G	0.000798403	0.0199641	intron-variant	NSMAF	GRCh38.p7	8:58585114	TAAGCAAACAATCTA[A/G]TGAATCTCCAAGAAA	8439
rs148669315	snp	A/T	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58596575	AACAGATACCCTGTA[A/T]ATGTTTGTCAAATGT	8439
rs148714602	snp	A/C	0.0535932	0.154675	intron-variant	NSMAF	GRCh38.p7	8:58617379	TGAACAGGCAACCTA[A/C]AGAATGGGAGAAAAT	8439
rs148783221	in-del	-/TG	0.00199481	0.0315187	intron-variant	NSMAF	GRCh38.p7	8:58612829	CCCCATCATACACTC[-/TG]AAACCCTCAAGCAGG	8439
rs148818311	snp	C/G	0.00159617	0.0282053	intron-variant	NSMAF	GRCh38.p7	8:58654708	ATCACTAATTTCCAT[C/G]CTTGAGTGGAAATCT	8439
rs148862871	snp	C/T	0.000132264	0.00813109	missense	NSMAF	GRCh38.p7	8:58597396	ATTTACCTGGGGAAT[C/T]TGCCATAGAAGCATT	8439
rs148870150	snp	A/G	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58650946	TTCCACCCACTTAAC[A/G]TGGCCTGTAACAAAA	8439
rs148946537	snp	A/G	0.0599851	0.162463	intron-variant	NSMAF	GRCh38.p7	8:58646001	AGCCAAGATCGCGCC[A/G]CTGCACTCCAGCCTA	8439
rs148976415	snp	A/T	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58657755	ATAATTCAAATAAAT[A/T]TAAAACACATGGCGC	8439
rs148980935	snp	A/C	0.0252325	0.109451	intron-variant	NSMAF	GRCh38.p7	8:58586181	TTCCAAGATGTAAGG[A/C]TGAGATGACCCTTTG	8439
rs148981624	snp	G/T	0.00199481	0.0315187	intron-variant	NSMAF	GRCh38.p7	8:58598102	AATCTACTTGTCAGG[G/T]AGAGGACCTGTCATC	8439
rs148997894	snp	A/C	0.00478085	0.0486577	intron-variant	NSMAF	GRCh38.p7	8:58641894	GTTTCAGTTTGCTAC[A/C]TGTAGTTGTATTTTA	8439
rs149004252	snp	C/T	0.0174175	0.0916809	intron-variant	NSMAF	GRCh38.p7	8:58639325	AAGAAGAAGAAGACA[C/T]ACAAATGGCCAACAA	8439
rs149019489	in-del	-/C	0.178465	0.239547	intron-variant	NSMAF	GRCh38.p7	8:58653462	CCTAAAGCCTTAGGA[-/C]ACAGAATAGTGAAAA	8439
rs149032828	snp	C/T	0.00119737	0.0244387	intron-variant	NSMAF	GRCh38.p7	8:58620410	AAGATGCATCATCAA[C/T]GACTAGTAGTAAATA	8439
rs149155175	snp	C/T	0.000798403	0.0199641	intron-variant	NSMAF	GRCh38.p7	8:58610591	AGCAACCTAAATGAA[C/T]ATGATTGCAAAAAGG	8439
rs149185722	snp	A/G	0.00279162	0.0372561	intron-variant	NSMAF	GRCh38.p7	8:58624952	CATACATATGGTGAT[A/G]ATTAATTTTATATGT	8439
rs149202268	snp	A/G	0.0185938	0.0946107	upstream-variant-2KB	NSMAF	GRCh38.p7	8:58661115	GGAAGCTAATCCTCC[A/G]TGTTGACTTCTGATT	8439
rs149227756	snp	C/T	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58603556	TTGTTCAGCTATGTA[C/T]AAACAGTTCCAAGAT	8439
rs149258877	snp	A/G	0.00119737	0.0244387	intron-variant	NSMAF	GRCh38.p7	8:58647503	AATGTGATTCCCAAC[A/G]TTGAAGGTGGAGGCC	8439
rs149300701	snp	A/G	0.0103295	0.0711199	intron-variant	NSMAF	GRCh38.p7	8:58600253	GTGGGCATAGAGTCC[A/G]AGTCCACACCATTAG	8439
rs149317377	snp	C/T	0.131723	0.220251	intron-variant	NSMAF	GRCh38.p7	8:58644703	CACAATAGCAAAGAC[C/T]TGGAACCAACCCAAA	8439
rs149344037	snp	A/G	0.0252325	0.109451	intron-variant	NSMAF	GRCh38.p7	8:58590783	ACTCAATTGTTTTGG[A/G]AGAAATAAAGTATTA	8439
rs149346079	snp	A/G	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58621163	GTCCATTTGTACTCA[A/G]TGTTCAGTTCCTACT	8439
rs149360975	snp	A/G	0.00874735	0.0655527	intron-variant	NSMAF	GRCh38.p7	8:58633987	ATAACTAAAATGTAT[A/G]GTTTTATAATGAAAA	8439
rs149476649	snp	A/G	0.00318978	0.0398085	intron-variant	NSMAF	GRCh38.p7	8:58611556	CAACACATGTGAAAA[A/G]ACAGAGTTTCAGCAG	8439
rs149487246	in-del	-/CAAC			intron-variant	NSMAF	GRCh38.p7	8:58592911	CAAAAACAAAAACAA[-/CAAC]AACAAAAAAAAAACC	8439
rs149521321	snp	A/G	0.000798403	0.0199641	intron-variant	NSMAF	GRCh38.p7	8:58639467	AACAGTTGTTGGCAA[A/G]AGCGTGGAGAAAAGA	8439
rs149564750	snp	A/G	0.0111798	0.073925	synonymous-codon	NSMAF	GRCh38.p7	8:58595607	CAGTTTGGTGATGTT[A/G]TTCCAGGCCAGTGTT	8439
rs149592948	snp	C/T	0.00879672	0.0657342	synonymous-codon, intron-variant	NSMAF	GRCh38.p7	8:58659236	GTGCCGGGATCCACG[C/T]CCGGACCCCGCGCGG	8439
rs149643936	snp	G/T	0.172997	0.237846	intron-variant	NSMAF	GRCh38.p7	8:58655851	GGCGGAACTTGCAGT[G/T]GGCTGAGATCGTGCC	8439
rs149650758	snp	C/G/T	1.64787e-05	0.00287038	synonymous-codon	NSMAF	GRCh38.p7	8:58585987	TGTTCCTGTGCTGAG[C/G/T]ACATGGCGACTATCT	8439
rs149662501	snp	C/G	0.00438332	0.0466095	intron-variant	NSMAF	GRCh38.p7	8:58592746	ACAAAAATTAGCCAG[C/G]CACGATGGTGGGTGC	8439
rs149678977	snp	A/C	0.00557542	0.0525036	intron-variant	NSMAF	GRCh38.p7	8:58637040	CACACACACACACAC[A/C]CCCACACACAAACAC	8439
rs149714345	snp	A/T	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58587574	CAGCCGAACCCCTAG[A/T]CTTTTAAGGTCAGTT	8439
rs149742903	snp	A/G	0.00953873	0.0683987	intron-variant	NSMAF	GRCh38.p7	8:58654491	GGAGGCGGAGTTTGC[A/G]GTGAGCCAAGATCAT	8439
rs149787547	snp	C/T	0.00199481	0.0315187	intron-variant	NSMAF	GRCh38.p7	8:58613210	ATTTCTATGCAAACA[C/T]ATATATGTATCTAAA	8439
rs149890381	snp	C/G/T	0.00269863	0.0366342	synonymous-codon, missense	NSMAF	GRCh38.p7	8:58597505	TGTCTGCCCAAATTC[C/G/T]AAGATTTGCGTAAGC	8439
rs149924717	in-del	-/TAA			intron-variant	NSMAF	GRCh38.p7	8:58600768	TATCTCAGTGTGGTG[-/TAA]GGATACCAAGTAAAC	8439
rs149927505	snp	C/T	0.00874735	0.0655527	intron-variant	NSMAF	GRCh38.p7	8:58625677	TCTGTGTCCTTAAAC[C/T]GAAAATGAGTCTCTT	8439
rs149947487	snp	A/T	0.0023933	0.0345097	intron-variant	NSMAF	GRCh38.p7	8:58619691	CCATTTATAATACCA[A/T]CACAAATATGAAGTA	8439
rs149963470	snp	A/C	0.0023933	0.0345097	intron-variant	NSMAF	GRCh38.p7	8:58657341	AGAGCCGCCAGTGAA[A/C]TTACAATGAACAGGT	8439
rs149989927	snp	C/T	0.0325976	0.123435	intron-variant	NSMAF	GRCh38.p7	8:58609387	AGCAAGTGCCCCTGA[C/T]ATGACTGAAAACAGA	8439
rs149999640	snp	C/T	0.0185938	0.0946107	intron-variant	NSMAF	GRCh38.p7	8:58649926	GACAACAACTTCCTC[C/T]TCTAGTGGTTTATAA	8439
rs150019202	snp	C/T	3.29549e-05	0.00405911	missense	NSMAF	GRCh38.p7	8:58599804	GTCCTCCTTGTCTCT[C/T]TCCCAAATCCAACTT	8439
rs150048294	snp	A/G	0.000378903	0.0137589	synonymous-codon	NSMAF	GRCh38.p7	8:58603301	GGCCAGGTTGTTGAG[A/G]TGAAGGAGGTACTGA	8439
rs150104149	snp	C/T	0.00318978	0.0398085	intron-variant	NSMAF	GRCh38.p7	8:58586120	TTTCTTCAAAATCCT[C/T]GTACTTAAGCAATGA	8439
rs150112584	snp	C/T	0.00795532	0.062565	intron-variant	NSMAF	GRCh38.p7	8:58615347	TGGACCCATACGGCA[C/T]TTATGGAATACTATT	8439
rs150120245	snp	C/T	0.00557542	0.0525036	intron-variant	NSMAF	GRCh38.p7	8:58627324	CAAGGTTACCCACTT[C/T]CACCACTTCTATTCA	8439
rs150150191	snp	A/C			intron-variant	NSMAF	GRCh38.p7	8:58644286	CCCACAGGCTAAAGC[A/C]AATTGGAGAGATATT	8439
rs150271308	snp	A/G/T	0.0185938	0.0946107	intron-variant	NSMAF	GRCh38.p7	8:58633906	CTTCTATAAACTATT[A/G/T]AAAAAGTAGGTGGAG	8439
rs150273330	snp	A/G	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58657924	CAAAGCAGCATATAC[A/G]TGGAAATGCAAGTAC	8439
rs150306393	snp	C/T			intron-variant	NSMAF	GRCh38.p7	8:58611060	AAATATTATTTAGTT[C/T]GGTCTCAACACTTCC	8439
rs150322945	snp	C/T	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58651983	TAAACTTCAAGGATA[C/T]CATAAAAATAAGCAC	8439
rs150323981	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	NSMAF	GRCh38.p7	8:58660853	TCAAGGTTCATCTAT[A/G]TTGTAGCATGTATCT	8439
rs150327850	snp	A/C	0.00119737	0.0244387	intron-variant	NSMAF	GRCh38.p7	8:58589379	AATATCTGTATGTAC[A/C]TTTTAAGCTAAAAAT	8439
rs150330925	snp	C/T	1.64741e-05	0.00286998	missense	NSMAF	GRCh38.p7	8:58603285	CGTTGCAGCTGCGGT[C/T]GGCCAGGTTGTTGAG	8439
rs150358444	snp	C/T	0.000798403	0.0199641	intron-variant	NSMAF	GRCh38.p7	8:58605461	ATTCAATTTGGAGGA[C/T]GTTAAAATATAAGAG	8439
rs150411552	snp	A/G	0.0023933	0.0345097	intron-variant	NSMAF	GRCh38.p7	8:58639165	TGGCACGTGCTGTAC[A/G]CCCAGCTACTTGGGA	8439
rs150453888	in-del	-/CAA			intron-variant	NSMAF	GRCh38.p7	8:58629640	TAAAAACAACAACAA[-/CAA]CAACAAAAACAATTA	8439
rs150488651	snp	C/T	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58594000	AAAGGAGGCTGTTTC[C/T]GTCCTCTATCCTCAA	8439
rs150591467	snp	C/T	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58636772	ATGGCCCAAGGGCTG[C/T]AGTTTGCCAAGCCCT	8439
rs150636426	snp	A/G	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58654069	CTTTAAGTCACAGTC[A/G]GATAGATTTCTTGGG	8439
rs150658367	snp	G/T	0.0023933	0.0345097	intron-variant	NSMAF	GRCh38.p7	8:58608524	GGAAACTGCCCCGGA[G/T]TCCCAGAGTCAGGTC	8439
rs150658908	snp	C/T	0.000231512	0.0107565	missense	NSMAF	GRCh38.p7	8:58623250	GATGTTCTAGCTAAA[C/T]GAGACTGCAAAATAG	8439
rs150692077	snp	C/T	0.00676609	0.0577691	intron-variant	NSMAF	GRCh38.p7	8:58621147	TTGTTCCCTTCTTTG[C/T]GTCCATTTGTACTCA	8439
rs150719986	snp	A/G	0.000181271	0.00951855	missense	NSMAF	GRCh38.p7	8:58584128	TGCAATTTCCAGAAT[A/G]TAATTTGTCTGTCTT	8439
rs150775141	in-del	-/CT			intron-variant	NSMAF	GRCh38.p7	8:58598848	CCAACATGGTGAAAC[-/CT]CGTCACGACCAAAAA	8439
rs150791010	in-del	-/T	0.172997	0.237846	intron-variant	NSMAF	GRCh38.p7	8:58655477	GACCATAGCTCACTG[-/T]TAACCTTGGACTCCT	8439
rs150799495	snp	C/T	0.00119737	0.0244387	intron-variant	NSMAF	GRCh38.p7	8:58597188	ATAAAAGCGATTTGA[C/T]TTCCCTTACAGTCTA	8439
rs150850146	snp	C/T	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58587363	GCTCAGAAACTACTA[C/T]TTTGGAATTCTAGTT	8439
rs150870126	snp	A/G	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58645666	ACAATGCAGAGAACA[A/G]AAGAAAAGGTCAAAA	8439
rs150898090	snp	A/G	0.00517822	0.0506191	intron-variant	NSMAF	GRCh38.p7	8:58655329	CCAACACTCCACGGT[A/G]GATAGTAAAGCAAAA	8439
rs150902909	snp	C/G	0.000798403	0.0199641	downstream-variant-500B	SDCBP, NSMAF	GRCh38.p7	8:58583189	TAGTGTGGTCTGACT[C/G]AAGTTTTTTCTCCTA	8439
rs150953038	snp	C/T	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58626837	CCAGCAGTGTAAAAG[C/T]GCTCCCTTTTCACCA	8439
rs150970885	snp	G/T	0.00199481	0.0315187	intron-variant	NSMAF	GRCh38.p7	8:58610769	ATGCTGTCGACTGAG[G/T]TGCAAAACAAGGGAA	8439
rs150981925	snp	A/G	0.306679	0.24349	intron-variant	NSMAF	GRCh38.p7	8:58639300	ATAAAAAAAAAAAAA[A/G]AAGAAGAAGAAGAAG	8439
rs151004766	snp	A/G/T	0.00319106	0.0398404	intron-variant	NSMAF	GRCh38.p7	8:58623866	ATGTGTACAGAACCT[A/G/T]CTATGATAAAATCTG	8439
rs151015572	in-del	-/ACGAA/CGAA/GA/TT	0.443908	0.157796	intron-variant	NSMAF	GRCh38.p7	8:58623301	CCAGAAAAAAAGTAT[-/ACGAA/CGAA/GA/TT]TTATAAGTATTTATA	8439
rs151028316	snp	C/G/T	0.00119737	0.0244387	intron-variant	NSMAF	GRCh38.p7	8:58612710	AGGCAGACAATGAAT[C/G/T]GAATTGTAGAATACC	8439
rs151047902	snp	A/G	1.66838e-05	0.00288818	missense	NSMAF	GRCh38.p7	8:58590022	ACATTATTATCCCAT[A/G]AAGAAGTTATGACAG	8439
rs151164453	snp	C/T	0.0134861	0.0810011	intron-variant	NSMAF	GRCh38.p7	8:58589369	AGTGGCTTATAATAT[C/T]TGTATGTACATTTTA	8439
rs151180209	snp	A/G	0.00478085	0.0486577	intron-variant	NSMAF	GRCh38.p7	8:58632001	GTCCTTACATAGTAT[A/G]TTAATAACTATGTGG	8439
rs151184016	snp	A/G	0.000798403	0.0199641	intron-variant	NSMAF	GRCh38.p7	8:58646037	CAAGAGCGAGACTCC[A/G]TCTCAAAATCATCAT	8439
rs151206159	snp	C/T	1.6473e-05	0.00286988	missense	NSMAF	GRCh38.p7	8:58603272	TACTGGGAGAGGTCG[C/T]TGCAGCTGCGGTCGG	8439
rs151218098	snp	A/G	0.0162398	0.0886349	intron-variant	NSMAF	GRCh38.p7	8:58656857	ATAAAAAAAATTAGT[A/G]TAAGTATATACCAAA	8439
rs151241201	snp	G/T	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58649446	CTATTGGGAAGAAAT[G/T]ATTGTATTTTCCAAT	8439
rs151337681	snp	C/G	0.0599851	0.162463	intron-variant	NSMAF	GRCh38.p7	8:58639083	AGATCAGGAGATCGA[C/G]ACCATCCTGGCTAAC	8439
rs180829573	snp	A/G	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58628290	TAAAAATTCTACATG[A/G]TAATATTGGAAAAAC	8439
rs180833557	snp	A/G	0.00398564	0.0444627	intron-variant	NSMAF	GRCh38.p7	8:58612894	ACAGCAATTCAAATC[A/G]TGGGGCTCTTCACCG	8439
rs180833723	snp	A/C	0.000798403	0.0199641	intron-variant	NSMAF	GRCh38.p7	8:58639355	AGCATATGAAAAGAT[A/C]CTCAGCAGCCTTAAT	8439
rs180834416	snp	G/T	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58655150	GGCCTATTTATTTTT[G/T]AAATAGAGAAAAGGT	8439
rs180844868	snp	C/T	0.00199481	0.0315187	intron-variant	NSMAF	GRCh38.p7	8:58602410	TCTGATTAAGGAACA[C/T]ATATATATTCCAAGT	8439
rs180848184	snp	C/T	0.00636936	0.0560724	intron-variant	NSMAF	GRCh38.p7	8:58592465	ACATACCTAAACATA[C/T]TGTATACTAGAAGAA	8439
rs180864351	snp	C/T	0.00159617	0.0282053	intron-variant	NSMAF	GRCh38.p7	8:58622541	TAGGATTACAGGTGC[C/T]CGCCACCATGCCTGG	8439
rs181056367	snp	A/G			intron-variant	NSMAF	GRCh38.p7	8:58625678	CTGTGTCCTTAAACC[A/G]AAAATGAGTCTCTTG	8439
rs181059552	snp	A/G	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58649776	CACCTTCCACCATGA[A/G]TAAAAGCTCCCTGAG	8439
rs181066202	snp	C/T	0.00438332	0.0466095	intron-variant	NSMAF	GRCh38.p7	8:58606881	AAATGAAACATTATA[C/T]ATAAATTGCCTGTTA	8439
rs181073134	snp	C/T	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58633635	GAGCCCTGAATATAA[C/T]ACTTATTGAATCCAT	8439
rs181075508	snp	C/T	0.000798403	0.0199641	intron-variant	NSMAF	GRCh38.p7	8:58586926	TAAATTATAGTGAGC[C/T]GCCAAAGTGCCTGAA	8439
rs181078156	snp	A/G	0.00716266	0.059414	intron-variant	NSMAF	GRCh38.p7	8:58617608	AATCAAAACCACAAC[A/G]AGATACCATCTCATG	8439
rs181106136	snp	C/T	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58657199	AGTCAGTCTCTATGC[C/T]TCTGCTTTTGCAGGA	8439
rs181119457	snp	A/C	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58643175	GCTTTTCCATTCTTG[A/C]ATTTAACAAACATTT	8439
rs181166254	snp	A/G	0.000798403	0.0199641	intron-variant	NSMAF	GRCh38.p7	8:58597665	CAAATAATGACAGCA[A/G]CTATGTACCAGGATT	8439
rs181280024	snp	C/T	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58646119	AAATGATAGCAGAAA[C/T]CAATTTTACCATCCT	8439
rs181281545	snp	A/T	0.00159617	0.0282053	intron-variant	NSMAF	GRCh38.p7	8:58629007	TCTGATTATCATGTG[A/T]CTTGGTAAGGACATC	8439
rs181297328	snp	A/T	0.000798403	0.0199641	intron-variant	NSMAF	GRCh38.p7	8:58613359	AAATACATTGGAGTA[A/T]GGTTCTTGTATTGGT	8439
rs181399024	snp	A/G	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58593417	TGAAAGTGTTTAGTT[A/G]GATAGCACTTTGTCT	8439
rs181414322	snp	A/T	0.000798403	0.0199641	intron-variant	NSMAF	GRCh38.p7	8:58620671	ACAGGCATTTAAATT[A/T]ACTGTTATTGAAAAC	8439
rs181528893	snp	C/T	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58637965	AAACCCTATTAAAAT[C/T]CCAATGGCATTTTTA	8439
rs181540899	snp	A/C	0.000727082	0.0190529	intron-variant	NSMAF	GRCh38.p7	8:58601234	ACAAGTATGTTGTAT[A/C]TATACAATCAGAAAG	8439
rs181584517	snp	A/G	0.0154538	0.0865337	intron-variant	NSMAF	GRCh38.p7	8:58656697	TAGCCGGGCGTGGTG[A/G]CAGGCGCCTGTAGTC	8439
rs181600101	snp	C/T	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58641780	GCATTGCTAGATCAA[C/T]AGGTTAATGCACATG	8439
rs181602009	snp	C/T	0.000798403	0.0199641	intron-variant	NSMAF	GRCh38.p7	8:58624895	CTCCCTTCAGTTCTA[C/T]CAATGTTCGCTTCAT	8439
rs181604893	snp	A/G	0.0279526	0.114869	intron-variant	NSMAF	GRCh38.p7	8:58605784	ACTCGGGAGGCTGAG[A/G]CACAAGAATCACTTG	8439
rs181615215	snp	G/T	0.00398564	0.0444627	intron-variant	NSMAF	GRCh38.p7	8:58584940	GCCCAGACTTTTTAA[G/T]GTATACATTTAAGAA	8439
rs181706670	snp	G/T	0.00199481	0.0315187	intron-variant	NSMAF	GRCh38.p7	8:58634152	CCAGAGCAGTAGATG[G/T]TTGTCACTGTCTTCA	8439
rs181721905	snp	A/C	0.0040129	0.0446133	intron-variant	NSMAF	GRCh38.p7	8:58597840	ACTCAAGTAGAAACT[A/C]CTTATTGACATATAA	8439
rs181785544	snp	A/G	0.000798403	0.0199641	intron-variant	NSMAF	GRCh38.p7	8:58654593	TACTAGCATAATCAA[A/G]AATATTATACACTCA	8439
rs181800391	snp	A/G	0.00159617	0.0282053	intron-variant	NSMAF	GRCh38.p7	8:58638910	ATACATAAAAAACTC[A/G]AACAACTTGATAGTA	8439
rs181805347	snp	G/T	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58650475	AGCTTCCTTCCAACA[G/T]GCAAGCTTGCCTGAT	8439
rs181810828	snp	G/T	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58621965	CTGTTTAAAAGCTCT[G/T]TAGTTTAATTAGTTC	8439
rs181821805	snp	C/G	0.000399281	0.0141238	intron-variant	NSMAF	GRCh38.p7	8:58601825	ACAGAATGCCTTCAT[C/G]AAAATAATTCAGTGA	8439
rs181851130	snp	C/T	0.00755907	0.0610114	intron-variant	NSMAF	GRCh38.p7	8:58618021	TTGCAGGGACATGGA[C/T]GAAGCTGGAAACCAT	8439
rs181978585	snp	A/G	0.000798403	0.0199641	intron-variant	NSMAF	GRCh38.p7	8:58611015	AAGTAGCCTGACAGA[A/G]TAAGAGGTGGCTTGA	8439
rs181995138	snp	C/G	0.00159617	0.0282053	intron-variant	NSMAF	GRCh38.p7	8:58651430	TCTATCACTCAGCTG[C/G]ACTCTAGAAAATTAC	8439

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