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

NEB

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs79562044	snp	C/T	1.8025e-05	0.00300203	missense	NEB	GRCh38.p7	2:151568082	TTACCTCACTCTGAA[C/T]GTCATTGCAGTGATG	4703
rs79570201	snp	A/G	0.172997	0.237846	intron-variant	NEB	GRCh38.p7	2:151535993	CTCACTGCAACCTCC[A/G]CCTCCCAGGCTCCAT	4703
rs79572798	snp	C/G	0.0509478	0.151255	intron-variant	NEB	GRCh38.p7	2:151708187	TCTACTGGATTCTTT[C/G]CATCAACATGATGCT	4703
rs79578929	snp	G/T	0.0425829	0.139564	intron-variant	NEB, RIF1	GRCh38.p7	2:151522192	GTATTTGAAGTTTAA[G/T]ATCTAATTTTTTAGC	4703
rs79649508	snp	C/T	0.0482946	0.147699	intron-variant	NEB	GRCh38.p7	2:151691420	TATTAGTTTCCTTAT[C/T]ATTGCTTGATATCTT	4703
rs79684655	snp	C/G	0.0123036	0.0774623	intron-variant	NEB	GRCh38.p7	2:151683322	TGCACTCGTTAATTT[C/G]CATAAGAGGGCGGTT	4703
rs79710954	snp	A/G	0.0225045	0.103662	intron-variant	NEB, RIF1	GRCh38.p7	2:151532732	ACAAGTTGCTAAGAG[A/G]AAAGCTCAATTAACT	4703
rs79717294	snp	G/T	0.0252325	0.109451	intron-variant	NEB	GRCh38.p7	2:151683976	TCACAAAGAGACAAA[G/T]ACTGTATGACTTTAC	4703
rs79722563	snp	C/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151577998	AGAATTCGATCACTA[C/G]TTCCACAATTTTGGT	4703
rs79767074	snp	A/T	0.0919752	0.193722	intron-variant	NEB, RIF1	GRCh38.p7	2:151504669	TTTTATTGGCCATAA[A/T]CTATTTCCCAAACTT	4703
rs79787361	in-del	-/AT	0.00478085	0.0486577	intron-variant	NEB	GRCh38.p7	2:151648303	TTCTTTTTCCTGCAC[-/AT]GTTTGTTATGGTGCA	4703
rs79832534	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151635445	AGAGTGTGACCTCAC[A/G]CTTGTAAAACCAGCA	4703
rs79843913	snp	C/T	0.00478085	0.0486577	intron-variant	NEB	GRCh38.p7	2:151559126	CCATCAAAAAGTAGG[C/T]GAAGGATATGAACAG	4703
rs79849542	snp	G/T	0.081446	0.184634	intron-variant	NEB	GRCh38.p7	2:151568792	GATACACTAAATTTA[G/T]AGTCCTTCTCTACTA	4703
rs79875240	snp	A/G	0.00745311	0.0605888	intron-variant	NEB	GRCh38.p7	2:151636348	CTCTAAATTTGGGGG[A/G]AAAAAAATCAGATGC	4703
rs79910490	snp	A/T	0.00874735	0.0655527	intron-variant	NEB	GRCh38.p7	2:151686302	CATTTTGCCTGGATA[A/T]TATGTGAGAATGACT	4703
rs79949067	snp	C/T	0.0879971	0.190408	intron-variant	NEB	GRCh38.p7	2:151681517	ACATCCCAGTTAGCA[C/T]CATCACTCTTTCGGC	4703
rs79988094	in-del	-/TG			intron-variant	NEB, RIF1	GRCh38.p7	2:151491052	CTTTTTTTTTTTTTT[-/TG]AGATGGGGTCTCTGT	4703
rs80039460	snp	A/G	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151672785	TGTGACTTTCTCAAG[A/G]GTGTACAAAAAATGC	4703
rs80040840	snp	G/T	0.0341408	0.126114	intron-variant	NEB	GRCh38.p7	2:151648166	AATTACATGTACTAT[G/T]TTTTCAACTTTTCTG	4703
rs80067206	snp	C/T	0.0310518	0.120672	intron-variant	NEB	GRCh38.p7	2:151734111	AGCGTATCTTCTTTT[C/T]CACACTAATATATTT	4703
rs80067588	snp	C/T	0.0126979	0.078662	intron-variant	NEB	GRCh38.p7	2:151638733	TCTGGAATGATGGCA[C/T]GTGGCCCTGTGCACA	4703
rs80103154	snp	C/T	0.0134861	0.0810011	intron-variant	NEB	GRCh38.p7	2:151689791	GATGTTAGTGTTTAG[C/T]TGTTCTTTATTGGGA	4703
rs80129179	snp	C/T	0.5	0	intron-variant	NEB	GRCh38.p7	2:151717857	TACCTCCTTTGTTCT[C/T]TTTTTTTTTTTTTTG	4703
rs80134779	snp	A/C			missense	NEB	GRCh38.p7	2:151682712	CCATTTCTAAGGACC[A/C]AAAAGGCACCCAGCC	4703
rs80163017	snp	C/T	0.00119737	0.0244387	intron-variant, missense	NEB, RIF1	GRCh38.p7	2:151533503	CGCAGAATTTCATTA[C/T]ATCCATGTTGCAGAA	4703
rs80168331	snp	C/T	0.0205511	0.0992634	intron-variant	NEB	GRCh38.p7	2:151661996	TCTTTTTTTTTTTAA[C/T]GACAAGACTCTTTTT	4703
rs80175539	snp	A/C	0.00358779	0.0422022	intron-variant	NEB	GRCh38.p7	2:151657590	ATCAACTATCATGAG[A/C]CCAAATGATCAGCAC	4703
rs80202061	snp	C/T	0.0287284	0.116357	intron-variant	NEB	GRCh38.p7	2:151693313	GCAGGATTGTGGGTT[C/T]GTTACATAGGGAAGC	4703
rs80212211	snp	C/T	0.00398564	0.0444627	intron-variant	NEB, RIF1	GRCh38.p7	2:151487304	TAATAAGTGATAATA[C/T]CAAAAGTTTCTTCCT	4703
rs80232472	snp	A/G	0.0119837	0.0764738	NEB	2	allele_origin=G(germline)/A(germline)	2:151675397	TGTATAAGATCTGCA[A/G]TAAAATGCATTTCAC	4703
rs80240836	snp	C/T	0.0475351	0.146656	intron-variant	NEB	GRCh38.p7	2:151696231	TCATGTACTGAATAC[C/T]TGCTGTTGGCCAGGG	4703
rs80255720	snp	C/T	0.000532526	0.0163089	synonymous-codon	NEB	GRCh38.p7	2:151717458	GGCAAATTCTATATC[C/T]GGAGGATCAGCCAGA	4703
rs80264058	snp	C/G	0.0130921	0.0798413	intron-variant	NEB	GRCh38.p7	2:151670600	ATTCTAAGATTGCCT[C/G]TCAGAACATGGAGCT	4703
rs80293781	snp	A/G	0.0352966	0.128072	intron-variant	NEB, RIF1	GRCh38.p7	2:151526786	CTCACAGGACAGGCC[A/G]TAATTCAGGACCCAT	4703
rs80294572	snp	A/G	0.0452528	0.143452	intron-variant	NEB	GRCh38.p7	2:151710004	TCTTGGCTACCAAGA[A/G]AGATCTCTTAAGGGC	4703
rs80301875	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151684751	CATCTTTTTAAAAGA[G/T]GGGCTACAGAAACCC	4703
rs80320923	snp	A/G	0.00516322	0.0505465	NEB	2	allele_origin=G(germline)/A(germline)	2:151612222	ATTCTTTGCTAGGAC[A/G]ATTTCCGGAGTGTCG	4703
rs80344795	snp	A/G/T	1.65767e-05	0.00287891	missense, stop-gained	NEB	GRCh38.p7	2:151656263	TGGTGATGTTGGCTT[A/G/T]GGCATCCTTTGCAGC	4703
rs80347254	snp	A/C	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151555803	TAGATTTTTCCAAAA[A/C]AGAAAATCAGCTTCT	4703
rs80354608	snp	C/T	0.0170251	0.090679	intron-variant	NEB	GRCh38.p7	2:151552275	TTTTCATAAGCCTTA[C/T]AGATAATGTGTGGTA	4703
rs111228003	snp	C/T	0.0429648	0.14013	intron-variant	NEB, RIF1	GRCh38.p7	2:151532139	TCTTACTCTGTCACC[C/T]AGGCTGGAGTGCAGT	4703
rs111241479	snp	C/T	9.29999e-05	0.00681845	synonymous-codon	NEB	GRCh38.p7	2:151671224	ATACTCGTCTTTATA[C/T]ACATTCTGTAAAAGG	4703
rs111279988	snp	C/G/T	3.31587e-05	0.00407164	splice-donor-variant	NEB	GRCh38.p7	2:151554930	GCATGACCGTACTTA[C/G/T]ATCGATGTTAAGCTT	4703
rs111280849	snp	A/G	0.5	0	intron-variant	NEB, RIF1	GRCh38.p7	2:151513193	CTAAGATGCCTAAAA[A/G]CTGTTCTAAACTTAG	4703
rs111288905	snp	A/G/T	0	0	splice-acceptor-variant, intron-variant	NEB, RIF1	GRCh38.p7	2:151494255	TCTTTGTACAAAACC[A/G/T]ATGGGAATCCAATGG	4703
rs111290910	snp	A/C			splice-acceptor-variant	NEB	GRCh38.p7	2:151568418	TTTCCGGTATTTAAT[A/C]TAAAAAAAAAAAAAT	4703
rs111293259	snp	C/G/T	0	0	splice-donor-variant	NEB	GRCh38.p7	2:151677564	ATTTTATTGTACTCA[C/G/T]ATCACTGACTTGCTT	4703
rs111300270	snp	C/T			splice-acceptor-variant	NEB	GRCh38.p7	2:151725561	CTCCTTGTATTTATT[C/T]TGAAAAGAATATCAG	4703
rs111314898	snp	A/C/G	4.96824e-05	0.00498385	intron-variant	NEB, RIF1	GRCh38.p7	2:151514431	TCCTGTACTCTTTCT[A/C/G]TATCATGAAAGAAAA	4703
rs111321902	snp	C/T	0.00517822	0.0506191	intron-variant	NEB	GRCh38.p7	2:151669537	AGGTAACATTTACAC[C/T]CAAACTTGGAGAGAG	4703
rs111332717	snp	G/T	0.5	0	intron-variant	NEB	GRCh38.p7	2:151723758	CTTCTTTGTTTTTTT[G/T]TTTTTTTTTTTTTTT	4703
rs111348513	snp	C/T	0.5	0	intron-variant	NEB	GRCh38.p7	2:151692622	CGCACACCAATGCTG[C/T]CTTTTTTTAAATAAT	4703
rs111350459	snp	A/G	0.00795532	0.062565	intron-variant	NEB	GRCh38.p7	2:151678967	TAAAGTGGTGTTTGG[A/G]ACTCTGGGAAGTCAA	4703
rs111354048	snp	C/T	0.0494327	0.149241	intron-variant	NEB	GRCh38.p7	2:151681816	CACTGAATTATAATT[C/T]ATACATTACTTCAAA	4703
rs111361047	snp	A/T	0.0170251	0.090679	intron-variant	NEB	GRCh38.p7	2:151544853	GTGAAGCCACAATAC[A/T]GAATGGTGAATGCAC	4703
rs111387118	snp	G/T	0.00953873	0.0683987	intron-variant	NEB	GRCh38.p7	2:151726736	CTTTTTAAAATCCTT[G/T]TGTACAGGGCTGGGC	4703
rs111390846	snp	G/T	0.5	0	intron-variant	NEB	GRCh38.p7	2:151556762	CAACACAATAATAGT[G/T]GGAGACTTTAACACC	4703
rs111404077	snp	C/T	0.000643945	0.017932	intron-variant	NEB	GRCh38.p7	2:151706876	TTTGACAAAAATATA[C/T]TTACGTCACTTAGGG	4703
rs111411188	snp	C/T	0.00795532	0.062565	intron-variant	NEB	GRCh38.p7	2:151724703	CAGGCCACTCAGTCA[C/T]CTGTGCAGCCTCCTT	4703
rs111428600	snp	C/G	0.105214	0.203807	intron-variant	NEB	GRCh38.p7	2:151556922	GAAAGCAGGAAAGAT[C/G]TAAAACTGACACCCT	4703
rs111438984	snp	C/T	0.348794	0.229651	intron-variant	NEB	GRCh38.p7	2:151609313	GTACTTCCAAAAAAG[C/T]AAGACCTGAGATCTC	4703
rs111458459	snp	A/G	0.00993419	0.0697739	intron-variant	NEB, RIF1	GRCh38.p7	2:151510614	CACATTCATGTAACT[A/G]TATAACTTTTATTAC	4703
rs111462227	snp	C/G	0	0	intron-variant	NEB, RIF1	GRCh38.p7	2:151500425	GAGTTGTATATAATA[C/G]ACAAATAATTTGTGT	4703
rs111476763	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151608221	CTACATGTCTTAGTA[A/T]TTAATATGAGGTCAA	4703
rs111486883	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151715712	CTGTGAGAAAATAAA[C/T]GTCTATTGTTTAAGC	4703
rs111508726	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151592254	ATATGAATAAAATTT[G/T]AAGTGAATTTTATAA	4703
rs111517514	snp	A/G	0.00101032	0.0224531	missense	NEB	GRCh38.p7	2:151547734	TACAATTCCCGATAC[A/G]GTCTCTACGTTGGAG	4703
rs111517947	snp	C/T	0.0225045	0.103662	intron-variant	NEB	GRCh38.p7	2:151695515	TGAATTGCAACAAAG[C/T]AGTTCAAACATAAAA	4703
rs111519651	snp	C/T	0	0	intron-variant	NEB	GRCh38.p7	2:151534982	GTACTAATTTTCTCA[C/T]GGAATTTTTGAACTT	4703
rs111538996	snp	C/T			splice-donor-variant	NEB	GRCh38.p7	2:151547428	CCTACGAGATGCTTA[C/T]ATCACTGGTGATGTC	4703
rs111542649	snp	C/T	0.00953873	0.0683987	intron-variant	NEB	GRCh38.p7	2:151573867	AAATAGTTTTTTTTT[C/T]CCTCAGTTGATTCTC	4703
rs111579221	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151605826	TTTTTTTTGAAACGC[A/G]GTTTCAGTCTTGTTG	4703
rs111586622	snp	C/T	0.00874735	0.0655527	intron-variant	NEB	GRCh38.p7	2:151696093	ATTTCTGGCCATTCA[C/T]CTATTGAGGTCACTT	4703
rs111610504	snp	A/G	0.00755907	0.0610114	intron-variant	NEB	GRCh38.p7	2:151708706	CTCTGACACTTCCAT[A/G]TGGATGTCTAAAAGG	4703
rs111613951	snp	C/T	0.0170251	0.090679	intron-variant	NEB, RIF1	GRCh38.p7	2:151531631	CACAACAATTCTTTA[C/T]TGGGGAGGAGAATCC	4703
rs111627031	snp	A/G	0.427423	0.176128	intron-variant	NEB	GRCh38.p7	2:151557453	TACAAGGAGGAGCTG[A/G]TACCATTCCTTCTGA	4703
rs111634348	snp	C/T			splice-donor-variant	NEB	GRCh38.p7	2:151694322	TTACAAAGAAACTCA[C/T]ATCACTCTGGTTTTT	4703
rs111635736	snp	A/C	0.0295035	0.117819	intron-variant	NEB	GRCh38.p7	2:151709005	TTCTCCAGCATAGCC[A/C]AGGCCAGGGTTAGAA	4703
rs111636984	snp	A/C/G	0	0	splice-acceptor-variant, intron-variant	NEB, RIF1	GRCh38.p7	2:151529315	TTCTTTGTATTTCAG[A/C/G]TGTGGGAGGAAACAC	4703
rs111640101	snp	C/T	0.0170251	0.090679	intron-variant	NEB	GRCh38.p7	2:151536785	AGGTGGTTTGCCCCA[C/T]GTCATACATTATTTG	4703
rs111643891	snp	C/T			splice-acceptor-variant, intron-variant	NEB, RIF1	GRCh38.p7	2:151514930	TTCCTATATTCTTTC[C/T]AATGTAAGTAGGAAG	4703
rs111691555	snp	C/T	0.0494327	0.149241	intron-variant	NEB	GRCh38.p7	2:151551418	ACAATTTCTAGTTCA[C/T]CTTTTATTGAGGTTA	4703
rs111701283	snp	A/C	0.0134861	0.0810011	intron-variant	NEB, RIF1	GRCh38.p7	2:151524020	TTAAGGCCTGGGGAG[A/C]GGTTCCAGTAGGATC	4703
rs111714967	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151547536	ATTTGTAGATCAACT[A/C]AAGAAAAAAAAATAC	4703
rs111740128	snp	A/C/G	0	0	splice-acceptor-variant	NEB	GRCh38.p7	2:151548416	TTCTTTGTACTTGAA[A/C/G]TGCAAAAGCAAAGTC	4703
rs111740664	in-del	-/ATGCGTGCTA	0.497933	0.032082	intron-variant	NEB, RIF1	GRCh38.p7	2:151495447	CTGCACGTTATTCTG[-/ATGCGTGCTA]GATGCGTGCTAATGT	4703
rs111753971	snp	C/T	0.00914312	0.0669923	intron-variant	NEB	GRCh38.p7	2:151648188	ACTTTTCTGAGTGCC[C/T]GAAATTATTTCAATA	4703
rs111768044	snp	A/C			splice-acceptor-variant, intron-variant	NEB	GRCh38.p7	2:151612390	AGATTTGTAAATAGC[A/C]TGAAAATGAAATAAT	4703
rs111833078	snp	C/G/T	0	0	splice-donor-variant, intron-variant	NEB, RIF1	GRCh38.p7	2:151514817	ACCAAGTGGGCACTA[C/G/T]CTCGCTTGCTATTTT	4703
rs111835809	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151500064	ATAATTTTGAAAATC[A/G]TTGCAAGCCTTTCAA	4703
rs111841612	snp	C/T	0.000583942	0.0170772	missense, intron-variant	NEB	GRCh38.p7	2:151630818	GCCTCTGTGTATAAA[C/T]GCTATAAAAGAAGAT	4703
rs111853076	snp	C/T	0.0178098	0.0926698	intron-variant	NEB	GRCh38.p7	2:151547350	AAGGCTGTTCAAAGA[C/T]CACTGGTTGTTTTAA	4703
rs111853129	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151568420	TCCGGTATTTAATCT[A/C]AAAAAAAAAAAATGA	4703
rs111863059	snp	C/T			splice-donor-variant, intron-variant	NEB	GRCh38.p7	2:151625533	AAACAAATGATCTTA[C/T]CTCACTATAATTTAT	4703
rs111868589	snp	A/G	0.0178098	0.0926698	intron-variant	NEB	GRCh38.p7	2:151641952	ATATCTCCTAATGCT[A/G]TCCCTCCTCCCTCCC	4703
rs111874021	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151590853	TGAGCCACCATGCCT[G/T]GCCTGAAATAATTTT	4703
rs111876441	snp	C/G	0	0	splice-donor-variant	NEB	GRCh38.p7	2:151562109	TAGGAAGGTGGCTCA[C/G]CTGACTCTGAAGGTC	4703
rs111912709	snp	C/T			splice-donor-variant	NEB	GRCh38.p7	2:151570080	AATGCAGCCCACTCA[C/T]ATCGCTCTGCAGTTC	4703
rs111918477	snp	A/G	0.5	0	intron-variant	NEB	GRCh38.p7	2:151633147	ATCTGCTTCCAATAG[A/G]TAGTAGGCTCTGTCA	4703
rs111919312	snp	C/T	0.5	0	intron-variant	NEB	GRCh38.p7	2:151644724	AATTATGCCCATTGA[C/T]TGCTAATGATCCTGT	4703
rs111954480	snp	A/G	0.5	0	intron-variant	NEB	GRCh38.p7	2:151731224	CCATCTTAGAAATAC[A/G]CTTATAAAAGAGGCA	4703
rs111969069	snp	C/T	0.0444908	0.142359	intron-variant	NEB	GRCh38.p7	2:151610974	TTAACTCACATTTAA[C/T]TATAAAATAGCTCCT	4703
rs111971842	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151721273	ATCATGCTGTTTTCC[A/G]CTCCAAAATCTTATG	4703
rs111974018	snp	G/T	0.5	0	intron-variant	NEB	GRCh38.p7	2:151727242	CTTAGTCTGATCTTG[G/T]ATTTTTAAAATAAAT	4703
rs111994546	snp	A/C			splice-acceptor-variant	NEB	GRCh38.p7	2:151546444	CTCTTTGTATTTAAT[A/C]TGAGAGGCAAACACA	4703
rs112045384	snp	A/G	0.0111196	0.0737302	intron-variant	NEB	GRCh38.p7	2:151632468	ATCACCTGAGGTCAG[A/G]AGTTGGAGACCAGCC	4703
rs112046723	snp	G/T			splice-acceptor-variant, intron-variant	NEB, RIF1	GRCh38.p7	2:151492496	TCAGAATAAAGAACC[G/T]GATGCAGGAGAGACC	4703
rs112052554	snp	A/C	0.0349115	0.127424	intron-variant	NEB	GRCh38.p7	2:151607441	TTTGTCACTATAACA[A/C]TCTCCATGAGCAGAC	4703
rs112053477	snp	A/G	0	0	intron-variant	NEB	GRCh38.p7	2:151605599	GGACAACATAGGCAA[A/G]TTTGAACAAAGAGAG	4703
rs112057574	snp	C/G/T	0	0	splice-donor-variant, intron-variant	NEB, RIF1	GRCh38.p7	2:151513579	GAATAGTAGCACTGA[C/G/T]CTGACTGGCAATATC	4703
rs112099765	snp	A/G	0.00702507	0.0588488	intron-variant	NEB, RIF1	GRCh38.p7	2:151496246	GTTTTTAAAATCAGT[A/G]AGTAGTTTTTTTCTT	4703
rs112125369	snp	G/T	0.5	0	intron-variant	NEB	GRCh38.p7	2:151728114	CTGATTGTTGGGATT[G/T]CGTGGAATAAAAAGT	4703
rs112126396	snp	C/T	0.5	0	intron-variant	NEB	GRCh38.p7	2:151730789	CTTAACCATTGTCAG[C/T]AGGCCGCCTGTGCTA	4703
rs112129826	snp	C/T	0.0111196	0.0737302	intron-variant	NEB	GRCh38.p7	2:151578468	GGTTTGAGACCAGCC[C/T]GGCCAACATGATGAA	4703
rs112157472	snp	C/T	0.444444	0.157135	intron-variant	NEB	GRCh38.p7	2:151648909	GCAAGCTCAAGGACC[C/T]CAGCTGGCCCGGGTT	4703
rs112163856	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151608312	TGTATGTGTGGTAGA[A/G]GAAAGGCATGTTGGT	4703
rs112173816	snp	C/G			splice-donor-variant	NEB	GRCh38.p7	2:151563822	AAAAGGTCATACTGA[C/G]CTCACTGTTCACCAG	4703
rs112199472	snp	C/T	0.5	0	intron-variant	NEB	GRCh38.p7	2:151686453	GCTATCAATGGGGAG[C/T]TATATCCTTCTTGAG	4703
rs112214144	snp	G/T			downstream-variant-500B, splice-donor-variant, utr-variant-3-prime, intron-variant	NEB, RIF1	GRCh38.p7	2:151485338	CATTCCATCCACAGA[G/T]TTGCAGAATTAGAGG	4703
rs112218633	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151630291	TTATGCCTAAGGTTT[C/T]CTTTCTATAGACAAA	4703
rs112229327	snp	A/C/T	0.5	0	synonymous-codon, missense	NEB	GRCh38.p7	2:151675380	ATCTTCTCCTTTAGC[A/C/T]TTGTATAAGATCTGC	4703
rs112238280	snp	A/T	0	0	intron-variant	NEB, RIF1	GRCh38.p7	2:151490369	AGCGCCAGGCACTTG[A/T]ACCTGTTGAGACTGC	4703
rs112255957	snp	A/C			splice-acceptor-variant	NEB	GRCh38.p7	2:151565149	TTCTTTATATTTTAC[A/C]TAAGGAGAGAAAACC	4703
rs112260335	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151602576	AAAGCAAATGATGTG[C/T]GCTGTCTTACATTGC	4703
rs112268049	snp	C/T	0.0295035	0.117819	intron-variant	NEB	GRCh38.p7	2:151687192	AAATATTAATGCATA[C/T]ATTTTTCAAAGTGAA	4703
rs112288851	snp	A/G	0.0033771	0.0409529	intron-variant	NEB	GRCh38.p7	2:151724245	GACAGAAGTGGCAAT[A/G]GAGCAGACCCTTACC	4703
rs112305111	snp	A/C	0.0509478	0.151255	intron-variant	NEB, RIF1	GRCh38.p7	2:151531251	CTCTGCTAAGACTTC[A/C]GTGTTTCCAGCTGGC	4703
rs112308782	snp	C/T	0.00755907	0.0610114	intron-variant	NEB	GRCh38.p7	2:151708767	CTCTTGTCTGTCCTC[C/T]AAAAAAATTACCAAC	4703
rs112383145	in-del	-/TA	0.430136	0.173352	intron-variant	NEB, RIF1	GRCh38.p7	2:151494389	TTAGATGGAAAGTAG[-/TA]TATGTTTCCTAAGGA	4703
rs112384270	in-del	-/T	0	0	intron-variant	NEB	GRCh38.p7	2:151561599	TTTGGTTTCGAACAC[-/T]TTTTTTTTTTTATTA	4703
rs112387433	snp	A/G	0.00755907	0.0610114	intron-variant	NEB	GRCh38.p7	2:151688048	CATGGGAAAGATGTT[A/G]TAAAACTCCAGGGAA	4703
rs112395248	snp	A/C	0.00835141	0.0640778	intron-variant	NEB	GRCh38.p7	2:151721534	TGGCCTTCTCTGATT[A/C]CTCACACGTGTTCTG	4703
rs112396829	snp	C/T	0.00279162	0.0372561	intron-variant	NEB	GRCh38.p7	2:151710938	TAAGCTTTACAAACA[C/T]TCCTAGTTTTCCAGA	4703
rs112398596	snp	A/G	0.00835141	0.0640778	intron-variant	NEB	GRCh38.p7	2:151666917	GTATTACCTTAAAAC[A/G]TATTTGTATGAGTAA	4703
rs112402631	snp	C/T	0.0209421	0.100162	intron-variant	NEB	GRCh38.p7	2:151669863	CCAGATAACAGGTTA[C/T]TGCAGTTGTCCACAC	4703
rs112406355	snp	A/G	0.00835141	0.0640778	intron-variant	NEB	GRCh38.p7	2:151641086	CAGGCACAATTCTAG[A/G]TAAGTACCGCAGATT	4703
rs112409014	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151604552	GGGTCTGGCGATAAT[A/T]TACGCACATCGCTCT	4703
rs112409695	snp	C/T	0.0260105	0.111035	intron-variant	NEB, RIF1	GRCh38.p7	2:151533864	GTTATGTCTTCTTTC[C/T]TTCCATTAATTTTTG	4703
rs112425038	snp	C/G/T	0	0	splice-donor-variant	NEB	GRCh38.p7	2:151568617	ACAGCCATATACTTA[C/G/T]ATCATCGAGGATCTC	4703
rs112439433	snp	C/G			splice-donor-variant, intron-variant	NEB	GRCh38.p7	2:151631142	GGCAGCTAGGACTCA[C/G]CTTATTCATGTTGAG	4703
rs112443521	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151714622	GCCAACCTTCAGTGG[A/G]CCAAGGAGGACCCCT	4703
rs112450383	snp	C/G/T	0	0	splice-donor-variant, intron-variant	NEB, RIF1	GRCh38.p7	2:151514317	TCAGCTGTGGGCCTA[C/G/T]CTCATTGAGGATTTG	4703
rs112451354	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151609483	TAGTTGAAAATTTTT[A/C]AAGGAAAATTTTGCT	4703
rs112470247	snp	C/T	0.0146672	0.084371	intron-variant	NEB	GRCh38.p7	2:151722499	TTTGTGGGATAACTA[C/T]ACAAATGTGTTTTTG	4703
rs112479335	snp	A/G	0.0178098	0.0926698	intron-variant	NEB	GRCh38.p7	2:151544955	CAACCATTTACACTT[A/G]TGAAATGCCCTTTGG	4703
rs112486602	snp	C/T	0.5	0	intron-variant	NEB	GRCh38.p7	2:151640180	GGACGGGCCAGGTAT[C/T]ACACAATATTCCTCT	4703
rs112489183	snp	G/T	0.5	0	intron-variant	NEB	GRCh38.p7	2:151658752	AGAACGAAATTCTAG[G/T]ACTCTCATTTCCTTT	4703
rs112517981	snp	A/C/G/T	1.65999e-05	0.00288091	splice-donor-variant	NEB	GRCh38.p7	2:151671022	AAAGGAAAGCACTCA[A/C/G/T]ATCACTTAGCTGCTT	4703
rs112544116	snp	C/G/T	0	0	splice-donor-variant	NEB	GRCh38.p7	2:151565715	AATAGGCTTTGCGTA[C/G/T]CTGACTCATCATTTC	4703
rs112563738	snp	C/T	0.5	0	intron-variant	NEB, RIF1	GRCh38.p7	2:151512022	TACCCTCTCACTCTT[C/T]TTTTTTTTTTTTTTT	4703
rs112571469	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151590847	CAGGCATGAGCCACC[A/G]TGCCTTGCCTGAAAT	4703
rs112593877	snp	C/T	0.5	0	intron-variant	NEB, RIF1	GRCh38.p7	2:151527831	TCCGGGTGAAATGAT[C/T]CTTCAATCTCTCTAG	4703
rs112610938	snp	A/T			splice-donor-variant, intron-variant	NEB, RIF1	GRCh38.p7	2:151514316	GTCAGCTGTGGGCCT[A/T]CCTCATTGAGGATTT	4703
rs112638545	snp	A/T	0.00398564	0.0444627	intron-variant	NEB	GRCh38.p7	2:151685228	CAGCTTCTGCTTCAG[A/T]CAGGAACAGGAATGA	4703
rs112647729	snp	C/T	0.00953873	0.0683987	intron-variant	NEB	GRCh38.p7	2:151647163	TTGCCCATGCTGGAG[C/T]GCAATGGTGCAGTCT	4703
rs112650499	snp	C/T	0.5	0	intron-variant	NEB	GRCh38.p7	2:151666033	ATGGAGTAAGTGGCT[C/T]CTGTTTTTTCCTCCC	4703
rs112663437	snp	G/T	0.00342587	0.0412456	intron-variant	NEB	GRCh38.p7	2:151675245	AGTCTATAATTTTAT[G/T]GTCAGGTCCGAATTT	4703
rs112675925	snp	C/T	0.0130921	0.0798413	intron-variant	NEB, RIF1	GRCh38.p7	2:151487127	TTTATGGCCTTTTTC[C/T]ACCTTTCGAAGAGGT	4703
rs112687345	snp	G/T			splice-acceptor-variant, intron-variant	NEB, RIF1	GRCh38.p7	2:151493447	TCTTTGTACAATACC[G/T]AGGGAAGCCAAAAGA	4703
rs112740534	snp	C/T	0	0	intron-variant	NEB	GRCh38.p7	2:151625427	AATGGCATAAAAAGC[C/T]AACTAAGCTAACTGG	4703
rs112790025	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151728240	TATTTTTTTAAAACA[A/G]TTGAAAATCTTAAGT	4703
rs112806716	snp	C/T	0.00478085	0.0486577	intron-variant	NEB	GRCh38.p7	2:151647980	CTTGGGAAATACAGA[C/T]GGAATATTTAGGCAT	4703
rs112819259	snp	C/T	0.5	0	intron-variant	NEB	GRCh38.p7	2:151721474	CCTCTACTCAAAATG[C/T]CTTTCTTCATCACCA	4703
rs112823419	snp	A/G	0.5	0	intron-variant	NEB	GRCh38.p7	2:151569697	TTTTTGGATTTTAAA[A/G]TCTTGGCAACTTAAT	4703
rs112835303	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151636550	TTTGGGAGGCAGAGG[A/C]GGGTGGATCACCTGA	4703
rs112844109	snp	A/C	0.5	0	intron-variant	NEB	GRCh38.p7	2:151648358	GACCCTCAGCACCCA[A/C]ACAAAGCAAGGCTTG	4703
rs112856025	snp	A/T	0.5	0	intron-variant	NEB	GRCh38.p7	2:151615816	AGTTTTGATTGATTG[A/T]TGGGTATAATGGGTC	4703
rs112881575	snp	G/T	0.137187	0.223099	intron-variant	NEB	GRCh38.p7	2:151719690	TCAAGACCAGCCAGG[G/T]CAATACGGTGAAACC	4703
rs112901076	snp	A/G/T	0.5	0	intron-variant	NEB	GRCh38.p7	2:151557318	CCAAGACTAAACCAG[A/G/T]AAGAAGTCGAATCCC	4703
rs112916919	snp	C/T	0.0260105	0.111035	intron-variant	NEB, RIF1	GRCh38.p7	2:151491629	ATGAAAGTCATTGAC[C/T]CTAGCATACTAAATG	4703
rs112933443	snp	C/T	0.000399281	0.0141238	splice-donor-variant, intron-variant	NEB, RIF1	GRCh38.p7	2:151525957	GTGGTTGATCACTTA[C/T]ATCACTGACATGCTT	4703
rs112958786	snp	A/G	0.00241693	0.0346789	synonymous-codon	NEB	GRCh38.p7	2:151697205	AGTTATGGTCTGAGG[A/G]AAGAAGCCTTTGCCT	4703
rs112960449	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151670491	CATACAGACGTGGTA[C/T]GAGTCCACGGTGTAA	4703
rs112972844	snp	C/T	0.5	0	intron-variant	NEB	GRCh38.p7	2:151639788	TGTTCTTTCTTTCCT[C/T]ATTAATGTTTCTTTT	4703
rs112989597	snp	A/C/G	4.24854e-05	0.00460878	intron-variant	NEB	GRCh38.p7	2:151568719	TGCGATATTTTTTCT[A/C/G]TGGGAAAGAAAGCAT	4703
rs112997385	in-del	-/T	0.5	0	intron-variant	NEB, RIF1	GRCh38.p7	2:151509614	GGGGAGGAAGAGAGG[-/T]TTTTTTTTTGTTTGT	4703
rs113016451	snp	A/G	0.5	0	intron-variant	NEB	GRCh38.p7	2:151575654	TATAGCCCTGACTGG[A/G]TAACTTTCCAAACAA	4703
rs113019668	snp	A/C	0.5	0	intron-variant	NEB	GRCh38.p7	2:151643003	TTCAGGTCTAAATGT[A/C]TTGTGTCAATAAGAA	4703
rs113028370	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151528285	TGCACTATTAGGCAC[A/G]TTTCTTTCCTCATTC	4703
rs113048349	snp	A/G/T	0.0316863	0.121828	intron-variant, utr-variant-3-prime	NEB, RIF1	GRCh38.p7	2:151497725	GTATAACACCTGTGC[A/G/T]ATAAGAAAGCATCCA	4703
rs113057378	snp	C/T	0	0	intron-variant	NEB	GRCh38.p7	2:151605581	TGTTTCTTTCCTATG[C/T]TTGGACAACATAGGC	4703
rs113057763	snp	A/G	0.00451849	0.0473163	intron-variant	NEB, RIF1	GRCh38.p7	2:151531943	GAAGTTGTAGAGTGG[A/G]CTTTAAGGTATCTAA	4703
rs113064554	snp	A/G	0.0325976	0.123435	intron-variant	NEB	GRCh38.p7	2:151657068	TTTCTTCTACAGAGG[A/G]GAGATCTTGATCCAT	4703
rs113068669	snp	A/G	0.000149074	0.00863221	synonymous-codon	NEB	GRCh38.p7	2:151553978	TACCATGTCGGGCAC[A/G]ATGTGGATTTTCATC	4703
rs113074361	snp	C/T	0.5	0	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151508108	TCTTCCTTGTACTTT[C/T]TCTGGGAATAGATTC	4703
rs113091511	snp	C/G/T	0	0	splice-donor-variant	NEB	GRCh38.p7	2:151682661	CACCCAGTGGCTTTA[C/G/T]CTCATTGAGGATGTC	4703
rs113093598	snp	C/G	0	0	splice-donor-variant	NEB	GRCh38.p7	2:151662134	TTATTGAAAGACTTA[C/G]TTCGTTCATAATTTT	4703
rs113095802	snp	A/G	0.0471641	0.146142	NEB	2	allele_origin=G(germline)/A(germline)	2:151724252	GTGGCAATGGAGCAG[A/G]CCCTTACCTTGCTGA	4703
rs113100061	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151607927	TTGAAGACCTTGATA[A/G]AAAAGACAAACCTCC	4703
rs113124626	snp	C/T	0.00755907	0.0610114	intron-variant	NEB	GRCh38.p7	2:151721842	ACTCACACAATAAAA[C/T]TGGTATCATGTGCTA	4703
rs113127297	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151698683	CCCTCTGTTGCCCAG[A/G]CTGGAGTGCAGTGGC	4703
rs113130896	snp	A/T	0	0	splice-donor-variant, intron-variant	NEB, RIF1	GRCh38.p7	2:151514816	GACCAAGTGGGCACT[A/T]CCTCGCTTGCTATTT	4703
rs113163445	snp	G/T	0.0225045	0.103662	intron-variant	NEB	GRCh38.p7	2:151731787	AGTAAAAACTGTTAC[G/T]GGCATTATTATCATA	4703
rs113174390	snp	C/T	0.000380981	0.0137966	missense	NEB	GRCh38.p7	2:151672470	AGTTGACATTGGTAG[C/T]GACATCCTGGGCCAT	4703
rs113178448	snp	C/G			splice-donor-variant	NEB	GRCh38.p7	2:151540343	AGGAAGGGATGCATA[C/G]ATCACTGGCATTCCA	4703
rs113192566	snp	A/G	0.172997	0.237846	intron-variant	NEB	GRCh38.p7	2:151545305	TCTAGGCCAGGCGTG[A/G]TGGCTCACGCCTGTA	4703
rs113196091	snp	C/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151707546	AGCAGGGAGAAGGAG[C/G]CTTGCTTTTCCTTCT	4703
rs113203777	snp	A/G	0.0368353	0.130617	intron-variant	NEB	GRCh38.p7	2:151607432	GGTAGGTAATTTGTC[A/G]CTATAACACTCTCCA	4703
rs113208235	snp	A/G	0.00755907	0.0610114	intron-variant	NEB	GRCh38.p7	2:151723547	TTACACAAAATACAT[A/G]GTTTTGAATTCATCC	4703
rs113265574	snp	A/T	0.5	0	intron-variant	NEB	GRCh38.p7	2:151566232	GGCATTTAGACTAAA[A/T]GAGGGAAACTACACA	4703
rs113267675	snp	A/C	0.5	0	intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151534522	AGTGTGGGATAGGTC[A/C]GATTTATGACACCAA	4703
rs113277889	in-del	-/TAAG	0.467642	0.123012	intron-variant	NEB, RIF1	GRCh38.p7	2:151495738	TGACACTTTCATTTT[-/TAAG]TAAGTAAATTGATAA	4703
rs113290650	snp	A/G/T	0	0	splice-acceptor-variant, intron-variant	NEB, RIF1	GRCh38.p7	2:151493869	TCTTTGTATAACACC[A/G/T]GTGAGATACAAAGTC	4703
rs113294149	snp	A/C	0.029116	0.117091	intron-variant	NEB	GRCh38.p7	2:151706425	ATTGAACGGCTTAGT[A/C]GGGCTCTTAATAATT	4703
rs113313596	snp	A/G	0.5	0	intron-variant	NEB	GRCh38.p7	2:151632446	TTTGGGATGCTGAGG[A/G]GGGCAGATCACCTGA	4703
rs113316424	snp	A/C	0.353803	0.227431	intron-variant	NEB	GRCh38.p7	2:151608731	AACATGGTGAAACCC[A/C]ATCTCTACTAAAAAT	4703
rs113326313	snp	A/C			splice-acceptor-variant	NEB	GRCh38.p7	2:151680023	GGCTTTGTAAGCGAT[A/C]TGAAAGAGAAAAAAA	4703
rs113327506	in-del	-/AAAC	0.369142	0.219784	intron-variant	NEB, RIF1	GRCh38.p7	2:151509327	ATGTAGATGTAAGGA[-/AAAC]AAACAGTTCTCATTG	4703
rs113329444	in-del	-/CAAAA	0.157972	0.232445	intron-variant	NEB	GRCh38.p7	2:151698065	TGCGAGACTCCGTCT[-/CAAAA]CAAAACAAAACAAAA	4703
rs113332788	snp	C/G/T	0	0	splice-acceptor-variant, intron-variant	NEB, RIF1	GRCh38.p7	2:151516564	TTCTTTGTATTTCAC[C/G/T]TGGTGATAGAAAGCC	4703
rs113350185	snp	C/T	0.0134861	0.0810011	intron-variant	NEB, RIF1	GRCh38.p7	2:151505971	TTCAGATCTAATCTC[C/T]CCCTCATGAAAACCG	4703
rs113370810	snp	C/T	0.5	0	intron-variant	NEB	GRCh38.p7	2:151648443	CACCAGAGTTTCTCT[C/T]TAAAAAATTTTTTTA	4703
rs113389396	snp	A/G	0.00755907	0.0610114	intron-variant	NEB	GRCh38.p7	2:151722397	GTTCCTCTAACATAC[A/G]GTTTTCAAGGTCTAG	4703
rs113401628	snp	A/C/T	0.0365119	0.130094	intron-variant	NEB	GRCh38.p7	2:151706832	AGGAGAAAATTTTCA[A/C/T]CTCTTTTGCAGCTAA	4703
rs113401748	snp	C/G	0.0260105	0.111035	intron-variant	NEB	GRCh38.p7	2:151570024	TTAGTGTCATAAACT[C/G]TCTGGAAGTCATGGC	4703
rs113403461	snp	A/G	0.00126195	0.0250875	intron-variant	NEB, RIF1	GRCh38.p7	2:151526145	GCAGAACTCATGGGC[A/G]GCTGGGGGTTACCTC	4703
rs113406378	snp	A/G	0.0399052	0.1355	intron-variant, utr-variant-3-prime	NEB, RIF1	GRCh38.p7	2:151497319	AGTACCATGCCTCCT[A/G]AACAATTATATGAGG	4703
rs113424185	snp	C/T	0.0134861	0.0810011	intron-variant	NEB	GRCh38.p7	2:151685125	TGTTCATATGTTACA[C/T]ACCATTGAAATTCCC	4703
rs113439353	snp	C/T	0.0143086	0.0833639	missense, intron-variant	NEB	GRCh38.p7	2:151579373	CTTTCCTGGCTTGGA[C/T]CACATCATTCTGGTC	4703
rs113473971	snp	A/G/T	0	0	splice-acceptor-variant	NEB	GRCh38.p7	2:151549742	GTTTTGTATAGATTC[A/G/T]GCAGGAATGAGGAAG	4703
rs113481305	snp	C/T	0.0123036	0.0774623	intron-variant	NEB	GRCh38.p7	2:151571077	ATGGCACCATCTCGG[C/T]TCACCCCAAACTCTG	4703
rs113490103	snp	C/G			splice-donor-variant, intron-variant	NEB	GRCh38.p7	2:151627001	CAAATTGGGGGCTCA[C/G]CTTGTTCATATTGAG	4703
rs113491623	snp	C/T	0.00914312	0.0669923	intron-variant	NEB	GRCh38.p7	2:151544981	TTTGGCAAACATGCA[C/T]ATCTATTATGGCCAA	4703
rs113525641	snp	C/G	0	0	splice-donor-variant, intron-variant	NEB, RIF1	GRCh38.p7	2:151490371	CGCCAGGCACTTGTA[C/G]CTGTTGAGACTGCAA	4703
rs113548820	in-del	-/AACA	0.5	0	intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151507545	TACTAGGAGAATCTG[-/AACA]AACAGCCATCGCTAA	4703
rs113556383	snp	A/G	0.00755907	0.0610114	intron-variant	NEB	GRCh38.p7	2:151724462	AGGCATGCTTGCTCA[A/G]AGGTTGCCAATGGGT	4703
rs113558009	snp	C/G	0.00318978	0.0398085	intron-variant	NEB	GRCh38.p7	2:151709383	GCAAATAATAAATTA[C/G]GAAATATTGAAGATG	4703
rs113565762	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151493870	CTTTGTATAACACCT[A/G]TGAGATACAAAGTCA	4703
rs113585313	snp	A/G	0.00358779	0.0422022	intron-variant	NEB	GRCh38.p7	2:151692799	ATGTGGTAAAACCCC[A/G]TCTCTACTAAAAATA	4703
rs113609170	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151547741	CCCGATACAGTCTCT[A/C]CGTTGGAGGAAATAT	4703
rs113625363	snp	A/C			splice-acceptor-variant	NEB	GRCh38.p7	2:151675392	AGCCTTGTATAAGAT[A/C]TGCAATAAAATGCAT	4703
rs113643881	snp	A/G	0.5	0	intron-variant	NEB	GRCh38.p7	2:151642876	ATAGAGGCGCTAAGA[A/G]AAACAGAAAAACATG	4703
rs113664554	snp	C/T	0.0115144	0.0749975	intron-variant	NEB	GRCh38.p7	2:151732267	CTGTATTTATGTGCA[C/T]TATAGTTCCAAGCCT	4703
rs113666116	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151696105	TCATCTATTGAGGTC[A/G]CTTTTATTTTTTTAG	4703
rs113680966	snp	A/G	0.5	0	intron-variant	NEB, RIF1	GRCh38.p7	2:151516914	TGGGTAGCTGTAAAC[A/G]CTTTAAAATTATTAA	4703
rs113705260	snp	C/T	0.0123036	0.0774623	intron-variant	NEB	GRCh38.p7	2:151566145	TTTCTGCTATCGTCA[C/T]AAGAAAAGGCTTACC	4703
rs113722243	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151659612	GGCCCAAAAAAATTT[C/T]AATGGAAAAGTTGCT	4703
rs113736581	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151583940	ATAATACGATTTTGG[A/G]TCATTTCAGAGAGGA	4703
rs113747416	snp	A/G	0.00953873	0.0683987	intron-variant	NEB	GRCh38.p7	2:151722198	GTCAAATAACTTGTC[A/G]CTTTATAATACAGTG	4703
rs113750553	snp	A/G	0	0	intron-variant	NEB	GRCh38.p7	2:151673820	CTCACTGCAAGCTCC[A/G]CCTCCCGGGTTCACG	4703
rs113756301	snp	C/T	0.5	0	intron-variant	NEB	GRCh38.p7	2:151652505	GCTGAGATTATGGGA[C/T]GGGGCCACTGCACCC	4703
rs113766142	snp	G/T	0.0134861	0.0810011	intron-variant	NEB	GRCh38.p7	2:151618125	TAATATTTTGAAGTA[G/T]CACTAAGTAACTATG	4703
rs113767547	snp	A/T	0.0325976	0.123435	intron-variant	NEB	GRCh38.p7	2:151657072	TTCTACAGAGGGGAG[A/T]TCTTGATCCATGGAG	4703
rs113786286	snp	A/C	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151681788	GCCTCAAGATCATCA[A/C]TATTTTTTCTTACAC	4703
rs113800731	snp	C/T	0.5	0	intron-variant	NEB	GRCh38.p7	2:151673073	GTACCAGCTATAGGA[C/T]AGCTGGGCCTTCACT	4703
rs113803601	snp	C/G/T	0	0	splice-donor-variant, intron-variant	NEB	GRCh38.p7	2:151630714	AGATTTTTGCTCCTA[C/G/T]CTCACTGTAGTTGAT	4703
rs113807294	snp	A/C	0.00716266	0.059414	intron-variant	NEB	GRCh38.p7	2:151729509	GAGTGATCCTCTGTC[A/C]GATAATCCCTTTTGC	4703
rs113815852	in-del	-/AA	0.5	0	intron-variant	NEB	GRCh38.p7	2:151658310	AATACCAGAAAAAGT[-/AA]AAGTTACTGGTCTCT	4703
rs113868334	snp	A/G	0.5	0	intron-variant	NEB	GRCh38.p7	2:151660701	CTACTCAACTCTGCT[A/G]TTGTAGTCCAAAAGC	4703
rs113888767	snp	G/T	0.0376037	0.131863	intron-variant	NEB	GRCh38.p7	2:151726533	GCCTCCAGAGGACAT[G/T]CAATCAAGCCACCCA	4703
rs113916636	snp	C/G/T	0	0	splice-donor-variant, intron-variant	NEB, RIF1	GRCh38.p7	2:151512732	TGACGAATGTCCTTA[C/G/T]CTGGCTTGAAAGATT	4703
rs113925788	snp	G/T			splice-acceptor-variant, intron-variant	NEB, RIF1	GRCh38.p7	2:151505572	TCCTTATACTTCACC[G/T]GCAGATTTAAAAATG	4703
rs113945095	snp	A/G	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151669553	CAAACTTGGAGAGAG[A/G]GGCAGAGGAAGAGCA	4703
rs113945302	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151648455	TCTTTAAAAAATTTT[G/T]TTATTTCCATATATT	4703
rs113948736	snp	A/T	0.5	0	intron-variant	NEB	GRCh38.p7	2:151609198	AACTCCATTTCAAAA[A/T]AAAAGAAAAAAAAAA	4703
rs113952741	snp	A/G/T	0.00747348	0.0606703	NEB	2	allele_origin=G(germline)/A(germline)	2:151640448	GTTCTTGTAGTCCAC[A/G/T]TCGCTGACTAAGGTC	4703
rs113976252	snp	C/T	0.00398564	0.0444627	intron-variant	NEB	GRCh38.p7	2:151719355	ACTGTGAAGTTTCTA[C/T]GATTATTTTCCCTTC	4703
rs114003449	snp	C/G	0.00953873	0.0683987	intron-variant	NEB, RIF1	GRCh38.p7	2:151492727	CTCATTTTCAAAGAA[C/G]GGGCACGGTATAATT	4703
rs114005738	snp	A/G	0.0115144	0.0749975	intron-variant	NEB, RIF1	GRCh38.p7	2:151503576	TTCAAGGAACAGGGG[A/G]GAAAATTCCATGAAT	4703
rs114072223	snp	C/T	0.0283406	0.115616	intron-variant	NEB	GRCh38.p7	2:151691347	CCACCCAACCTAAGA[C/T]GCCCATCCAGTCACT	4703
rs114076111	snp	A/G	0.0103295	0.0711199	intron-variant	NEB	GRCh38.p7	2:151688808	TCTGTCTCTCAAAAT[A/G]TCTTACTGTATGTTT	4703
rs114076205	snp	A/G	0.0186264	0.0946902	synonymous-codon	NEB	GRCh38.p7	2:151684781	CTGGTTACTCACATC[A/G]CTCTGCAGCGCATAT	4703
rs114082480	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151654606	TGTGTTAAAACTGGG[C/T]AATAACAAAAATAGC	4703
rs114089598	snp	C/T	0.00486875	0.0490986	missense	NEB	GRCh38.p7	2:151667874	CTCAAATCATAGCCC[C/T]TGGCAATGGTTTTCT	4703
rs114105852	snp	A/G	0.00119737	0.0244387	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151499115	TTTTTATTAAGTTAA[A/G]TGATTATATTAATGT	4703
rs114111587	snp	C/T	0.00318978	0.0398085	intron-variant	NEB	GRCh38.p7	2:151731036	ATTGTTTGATGCTGA[C/T]GCCACATAGAGTCAT	4703
rs114116625	snp	A/G	0.0168055	0.0901129	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151610118	GGCTTCCTTGTATTT[A/G]TACTAAAATGCCAGA	4703
rs114118829	snp	C/T	0.00874735	0.0655527	intron-variant	NEB	GRCh38.p7	2:151683313	TAAAACAGTTGCACT[C/T]GTTAATTTGCATAAG	4703
rs114124524	snp	A/T	0.0402882	0.136092	intron-variant	NEB	GRCh38.p7	2:151671594	GATCATGCTTTAGAC[A/T]GCATTATGCAACACA	4703
rs114157246	snp	A/G	0.00634325	0.0559588	intron-variant	NEB	GRCh38.p7	2:151553796	CCGTGGGGCGGGGCC[A/G]TGGAGGGGTACTTCT	4703
rs114160460	snp	A/G	0.0165278	0.0893908	intron-variant	NEB	GRCh38.p7	2:151723324	ATCTGGCCAGAATAT[A/G]TAATTCAAGTTCCCC	4703
rs114218081	snp	A/G	0.034155	0.126139	intron-variant, synonymous-codon	NEB, RIF1	GRCh38.p7	2:151533477	TGTAGAGAGCAGTCA[A/G]CATATCTGGACGCAG	4703
rs114238647	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151666031	GGATGGAGTAAGTGG[C/T]TCCTGTTTTTTCCTC	4703
rs114244531	snp	A/G	0.0912534	0.193131	intron-variant	NEB, RIF1	GRCh38.p7	2:151505909	TATCCAGGAAGGTTG[A/G]TTCTTTGACTGTACC	4703
rs114266322	snp	C/G	0.00159617	0.0282053	intron-variant	NEB, RIF1	GRCh38.p7	2:151504952	AGAGAGCAAAGAATA[C/G]AGGAGAAGAAACCTT	4703
rs114269303	snp	C/T	0.00716266	0.059414	intron-variant	NEB, RIF1	GRCh38.p7	2:151519511	GCTTAATGGTTATAG[C/T]TTCTGTTGGTATGAA	4703
rs114287777	snp	A/C	0.0364509	0.129988	intron-variant	NEB	GRCh38.p7	2:151623733	AATCTGTTTTTCTTC[A/C]AAATTTCTAGGAATG	4703
rs114290306	snp	C/G	0.0115144	0.0749975	intron-variant	NEB	GRCh38.p7	2:151656924	CAGTCATTTACTGAT[C/G]AGAAAAGTTTCAATT	4703
rs114308589	snp	C/T	0.0023933	0.0345097	intron-variant	NEB, RIF1	GRCh38.p7	2:151527852	ATCTCTCTAGTTCTG[C/T]CAGTCCAGCCTAATC	4703
rs114323121	snp	C/T	0.0119091	0.0762411	intron-variant	NEB	GRCh38.p7	2:151697702	TCACTCCCACGCTGA[C/T]TATAACACTTACATT	4703
rs114352852	snp	A/T	0.0174175	0.0916809	intron-variant	NEB	GRCh38.p7	2:151613884	CAGCCCATGGAAATG[A/T]AAGTCAATTAAACCT	4703
rs114353777	snp	C/T	0.0930568	0.194599	intron-variant	NEB, RIF1	GRCh38.p7	2:151510826	AAGAGGAGACTACTG[C/T]ATAGTATCCTAAATT	4703
rs114354356	snp	C/T	0.00478085	0.0486577	intron-variant	NEB	GRCh38.p7	2:151649470	CCTCCTAATAACAGA[C/T]GGTTATTATATATCT	4703
rs114404051	snp	A/C	0.0126979	0.078662	intron-variant	NEB	GRCh38.p7	2:151612499	AATCTTATTTGTGTA[A/C]ATTTCTGGGAAGACC	4703
rs114425507	snp	A/G	0.00398564	0.0444627	intron-variant	NEB	GRCh38.p7	2:151649248	GTCAGCATTTACTAT[A/G]CATTCTGGAAATCAG	4703
rs114427517	snp	A/G	0.0410537	0.137264	intron-variant	NEB	GRCh38.p7	2:151646841	TTTTAGTAGAAACAG[A/G]GTTTCGCTACGTTGT	4703
rs114457116	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151543273	TTCTAATCATGGATA[G/T]AAATACCAGTTGAAC	4703
rs114459145	snp	G/T	0.031825	0.122064	intron-variant	NEB	GRCh38.p7	2:151710124	AATTTGGCTCCTCAG[G/T]CAAAGAATAATTAAA	4703
rs114549990	snp	A/G	0.0240643	0.107019	intron-variant	NEB	GRCh38.p7	2:151536463	GTACATTAATTTGAA[A/G]AGTTTTCCAGTAATT	4703
rs114556700	snp	A/G	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151728369	GACTAAGGGAAAATT[A/G]GTCGTTTGTTCTGCA	4703
rs114570062	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151682434	TGGTTAACAAGTTAT[A/G]CCTTAATAAAATTGT	4703
rs114574356	snp	C/T	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151609296	GATAAGTGCACGAGA[C/T]TGTACTTCCAAAAAA	4703
rs114622020	snp	A/C	0.00279162	0.0372561	upstream-variant-2KB	NEB	GRCh38.p7	2:151735710	TGAGAAAGTAATCTC[A/C]TATTTCAAATACATG	4703
rs114650981	snp	A/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151696187	CTCAGAGATTCCAAT[A/T]TCCAGAAACTTACTA	4703
rs114687041	snp	A/G	0.0955749	0.196603	intron-variant	NEB, RIF1	GRCh38.p7	2:151496144	AGCCCAAAGGAAAAA[A/G]GGGTAAATTTGCTAA	4703
rs114798570	snp	A/G	0.0138799	0.0821421	intron-variant	NEB, RIF1	GRCh38.p7	2:151488001	TATGTACTTTATCTT[A/G]TTTTTATATTCTTGG	4703
rs114798617	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151692597	CCTAATATTTTTTCA[A/G]ACTGAAAAACGCACA	4703
rs114807972	snp	G/T	0.00597247	0.0543191	intron-variant	NEB	GRCh38.p7	2:151681322	TTATTAAGAGAGACA[G/T]GACTTTTGCTCTGCA	4703
rs114812442	snp	A/G	0.0418186	0.138422	intron-variant	NEB	GRCh38.p7	2:151630026	GTAGAACAATGTTTA[A/G]TATCTATCTATACGT	4703
rs114844916	snp	A/T	0.0352966	0.128072	intron-variant	NEB	GRCh38.p7	2:151653007	ATAATATATCATCAT[A/T]TTAATTTTCCAACAT	4703
rs114853127	snp	C/T	0.00509621	0.0502208	missense, intron-variant	NEB	GRCh38.p7	2:151642612	CCTTGGCTGCCTTGA[C/T]AGGAATGGCATCTAC	4703
rs114879584	snp	C/T	0.00279162	0.0372561	intron-variant	NEB, RIF1	GRCh38.p7	2:151508270	TCGCAAGGAAGAACC[C/T]TCTCAGTCAAAGAAA	4703
rs114945174	snp	C/T	0.0197687	0.0974348	intron-variant	NEB, RIF1	GRCh38.p7	2:151503707	GCATTAATAAATAAA[C/T]TTACCAATGAGAAAA	4703
rs114945675	snp	C/G	0.0372196	0.131242	intron-variant	NEB	GRCh38.p7	2:151695375	TACGATTATCTAATT[C/G]TATGAAATTACTTAT	4703
rs114950505	snp	A/G	0.00358779	0.0422022	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151503144	CTTATAGTATTTCAA[A/G]TCTAGTCAAGTCACT	4703
rs114959904	snp	A/C/G	0.00392061	0.0441024	NEB	2	allele_origin=G(germline)/A(germline)	2:151684973	ATCTTTTCGATATTC[A/C/G]CGCTGTGAATAGGAA	4703
rs114983921	snp	C/T	0.0138799	0.0821421	intron-variant	NEB	GRCh38.p7	2:151695049	CTTAGTACTCATTTA[C/T]AGAATTATTGAAGAA	4703
rs114985345	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151630514	CACTGGAAATCACCA[C/T]GAACAGAAAAGACAT	4703
rs115003937	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151674590	TATAACAGACCTGGA[C/T]AGAAAAGCAAACAGA	4703
rs115013318	snp	A/G	0.00279162	0.0372561	intron-variant	NEB	GRCh38.p7	2:151651050	TCAGCCTCCCTAGTA[A/G]CTGGGATTTACAGGT	4703
rs115014990	snp	A/G	0.0341408	0.126114	intron-variant	NEB	GRCh38.p7	2:151708473	CACTTGCTTCCCAAC[A/G]CATTGCCCTCTCCTG	4703
rs115047526	snp	A/G	0.0158469	0.0875917	intron-variant	NEB	GRCh38.p7	2:151611478	ATACCCCAGACTCTG[A/G]AGTTTGCTATCTGAA	4703
rs115049343	snp	C/T	0.00478085	0.0486577	intron-variant	NEB	GRCh38.p7	2:151646846	GTAGAAACAGGGTTT[C/T]GCTACGTTGTGCAGG	4703
rs115092099	snp	C/T	0.0916144	0.193427	intron-variant	NEB, RIF1	GRCh38.p7	2:151504296	GCTTCTAGGAACCTT[C/T]GAACATCTACCTTCT	4703
rs115096433	snp	A/G	0.0178098	0.0926698	intron-variant	NEB	GRCh38.p7	2:151689564	TTTTTAAAAGGTGAC[A/G]TTAGGTGTAAGGAAG	4703
rs115135596	snp	C/T	0.0232847	0.105357	intron-variant	NEB	GRCh38.p7	2:151673228	TGCTGTCCAAAGTCT[C/T]TCACTGCTGGAATCA	4703
rs115142419	snp	C/T	0.00140889	0.026504	intron-variant	NEB	GRCh38.p7	2:151551735	CAAGTTCTCACTGCT[C/T]ACCGAACTCTGGAGC	4703
rs115164333	snp	A/G	0.00597247	0.0543191	intron-variant	NEB, RIF1	GRCh38.p7	2:151491327	AACTTCCTTGATGCA[A/G]TAGAGCTCAGGAAGT	4703
rs115178773	snp	C/G	0.0244538	0.107838	intron-variant	NEB	GRCh38.p7	2:151714518	CCTGGGGAGCTGGAG[C/G]TTCATTCTGAAGGCT	4703
rs115187177	snp	C/T	0.00398564	0.0444627	intron-variant	NEB, RIF1	GRCh38.p7	2:151504889	GCTTAATGTATAATA[C/T]ACCATTGTAGGTAGA	4703
rs115197960	snp	A/C	0.02016	0.0983543	intron-variant	NEB	GRCh38.p7	2:151669820	TAAGACAGGCTCTTG[A/C]GATTGTTTGAGACCT	4703
rs115202632	snp	A/G	0.0228947	0.104514	intron-variant	NEB	GRCh38.p7	2:151720082	AGGAACCTTCTTCAG[A/G]ATTCTGTTTAGTTAG	4703
rs115204553	snp	C/G	0.00676609	0.0577691	intron-variant	NEB, RIF1	GRCh38.p7	2:151533783	AGCTAGTTTCACTTA[C/G]GTTACCACCAAAATA	4703
rs115263893	snp	G/T	0.0197687	0.0974348	intron-variant	NEB, RIF1	GRCh38.p7	2:151507622	TCACACTTCCGCATC[G/T]CTATCCATAAAAATA	4703
rs115266621	snp	A/G	0.093777	0.195178	intron-variant	NEB, RIF1	GRCh38.p7	2:151515413	ATATGGGGTCTTGCT[A/G]TGATGCCCAGGCTGG	4703
rs115350357	snp	C/T	0.00278659	0.0372227	missense	NEB	GRCh38.p7	2:151658000	CACTTGCAATATCTC[C/T]GGAAGCCTTGGCAGC	4703
rs115379999	snp	A/G	0.000880187	0.0209599	synonymous-codon	NEB	GRCh38.p7	2:151663593	CAATTCAAAGCTCAT[A/G]GCATCAGGAAGCATG	4703
rs115393086	snp	A/T	0.00953873	0.0683987	intron-variant	NEB	GRCh38.p7	2:151725635	CTCACCCCATTTGAT[A/T]AAAAAAAATCCTTCA	4703
rs115394251	snp	C/T	0.0777632	0.181203	intron-variant	NEB, RIF1	GRCh38.p7	2:151501528	ACCTGGACCCATCAT[C/T]TTTTAGGTAGACTTA	4703
rs115395951	snp	C/T	0.00478085	0.0486577	intron-variant	NEB	GRCh38.p7	2:151691417	CTGTATTAGTTTCCT[C/T]ATTATTGCTTGATAT	4703
rs115403439	snp	C/G	0.00914312	0.0669923	intron-variant	NEB	GRCh38.p7	2:151669270	CTCTGTCATAAGGGA[C/G]GGGCCCTGGTAGATG	4703
rs115454721	snp	A/C	0.0352966	0.128072	intron-variant	NEB	GRCh38.p7	2:151634731	CGAGGAGAATTTATT[A/C]TTATTATTATTATTT	4703
rs115456572	snp	A/C	0.021333	0.101051	intron-variant	NEB	GRCh38.p7	2:151668488	CTTTTAAAAAATTAA[A/C]AATTTTATCCAAGTT	4703
rs115480336	snp	C/G	0.0146672	0.084371	intron-variant	NEB	GRCh38.p7	2:151552585	AGAAAAGACTTGGCA[C/G]TGCCCAGTCTATGGT	4703
rs115481788	snp	A/G	0.00953873	0.0683987	intron-variant	NEB	GRCh38.p7	2:151574398	ATCCTGATATGAATG[A/G]GAAGTTTGGTCACTG	4703
rs115519843	snp	A/G	0.00398564	0.0444627	intron-variant	NEB, RIF1	GRCh38.p7	2:151495149	TTTGGCTCTTATATC[A/G]CTATCATGGCGAATC	4703
rs115538815	snp	C/T	0.0271762	0.113356	intron-variant	NEB, RIF1	GRCh38.p7	2:151510316	TTCATTATTTTGTTA[C/T]GCTTTAAGGCCCAGG	4703
rs115574522	snp	A/T	0.0209421	0.100162	intron-variant	NEB	GRCh38.p7	2:151727282	CACTATACACCTCTT[A/T]ACATACCTTTTTATA	4703
rs115575948	snp	C/T	0.0130921	0.0798413	intron-variant	NEB	GRCh38.p7	2:151628347	ACTCCCTGAAGTGGT[C/T]TGGATTATATTCCCA	4703
rs115579881	snp	G/T	0.00676609	0.0577691	intron-variant	NEB, RIF1	GRCh38.p7	2:151523070	ATTTCAACATCATAG[G/T]CGTTTGTTTTTAAAT	4703
rs115592041	snp	C/T	0.00557542	0.0525036	intron-variant	NEB	GRCh38.p7	2:151683063	CTGCACTTCAAAGAG[C/T]AAGTGAAATTGTCAG	4703
rs115606881	snp	A/G	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151665220	CCCCCTCCCACCACC[A/G]GCACGAAGACGATCA	4703
rs115607882	snp	A/G	0.0119091	0.0762411	intron-variant	NEB	GRCh38.p7	2:151717214	AATTACTGAGTCATC[A/G]AGCTGGCTAAACATT	4703
rs115610425	snp	C/T	0.0182019	0.0936463	intron-variant	NEB	GRCh38.p7	2:151712948	GTACTTGCAGTTGAA[C/T]GATGGAAACTTGGAA	4703
rs115623365	snp	A/G	0.000547486	0.0165361	missense	NEB	GRCh38.p7	2:151538241	ATGTTTCTTTGTAGC[A/G]TAGCTAGAAAGAGAA	4703
rs115624280	snp	C/G	0.00914312	0.0669923	intron-variant	NEB	GRCh38.p7	2:151675137	AAAAGGCCAACTGAA[C/G]AGGTAAAGAACCATC	4703
rs115625493	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151626935	AAAAAGAGACTAACT[C/T]AATTAACAATAGGTA	4703
rs115631125	snp	A/C	0.0166011	0.089582	NEB	2	allele_origin=A(germline)/C(germline)	2:151561253	AGTCACATAGAGGGG[A/C]GTGTCTGTGACCAGA	4703
rs115636003	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151672314	TCTAATAAAAGCGAG[A/C]AGTGATCATCCTTTA	4703
rs115642134	snp	A/G	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151720660	GATGAAGGGAGATAG[A/G]AGATTAACTGTCTTC	4703
rs115659414	snp	C/T	0.00755907	0.0610114	intron-variant	NEB	GRCh38.p7	2:151662604	ACTTGTTTTTCTCAA[C/T]GCCTTCATAAAGAAA	4703
rs115664356	snp	C/T	0.0494327	0.149241	intron-variant	NEB	GRCh38.p7	2:151693492	TCAACATTCAACTCC[C/T]ACTTGTAAGTAAGAA	4703
rs115715574	snp	C/G	0.0228947	0.104514	intron-variant	NEB	GRCh38.p7	2:151713408	CCTGCTTGACTCAAT[C/G]AAATCTCTTCTGGTG	4703
rs115730804	snp	A/G	0.108048	0.20579	intron-variant	NEB, RIF1	GRCh38.p7	2:151493284	TTGAATGAGAAAGGC[A/G]TGTTTTTATGATGTT	4703
rs115751282	snp	A/T	0.0322114	0.122752	intron-variant	NEB	GRCh38.p7	2:151688764	AAAAATTATAACAAA[A/T]CTGTAATAAAAGTTA	4703
rs115761880	snp	C/T	0.00597247	0.0543191	intron-variant	NEB, RIF1	GRCh38.p7	2:151532119	TGTTTCCCTCCGAGA[C/T]GGAGTCTTACTCTGT	4703
rs115768954	snp	G/T	0.00795532	0.062565	intron-variant	NEB	GRCh38.p7	2:151611277	AGAAAGGTACATAAC[G/T]CCTCACATTCCTCAT	4703
rs115781199	snp	G/T	0.0170251	0.090679	intron-variant	NEB	GRCh38.p7	2:151683156	ATAGAAGGCCACATT[G/T]AAGGTGGGTTATTTG	4703
rs115789938	snp	A/G	0.00755907	0.0610114	intron-variant	NEB	GRCh38.p7	2:151535078	CTAAATAAATTCATA[A/G]CTTGTTTATTTCAGC	4703
rs115820899	snp	A/G	0.00636936	0.0560724	intron-variant	NEB, RIF1	GRCh38.p7	2:151516751	GTTGAGGGGATGGGT[A/G]CCATTACTGTCTGCA	4703
rs115826291	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151496780	TGTATTATGGAAATG[A/G]TGTTAGGCTAGAAGT	4703
rs115829760	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151612037	AGAAGAGCACACCTT[C/G]AATTCAAGCAGATGC	4703
rs115831309	snp	C/T	0.0217236	0.101931	intron-variant	NEB	GRCh38.p7	2:151571762	AATAACAGAGAGACT[C/T]GGAAATAATAGTAAT	4703
rs115894166	snp	C/T	0.0228947	0.104514	intron-variant	NEB, RIF1	GRCh38.p7	2:151518704	GGTATTTCTATGTCC[C/T]TAGAGAAAAGGGAAT	4703
rs115986826	snp	G/T	0.00160994	0.0283263	missense	NEB	GRCh38.p7	2:151674478	AAATTTGTACTCACA[G/T]CACTGGCAATGTTTC	4703
rs115996307	snp	C/G	0.0154538	0.0865337	intron-variant	NEB	GRCh38.p7	2:151652704	AATTTATAAATACAA[C/G]GACATTTGAAATTGA	4703
rs116002357	snp	A/C/G	0.0134995	0.0811632	intron-variant	NEB	GRCh38.p7	2:151660442	GTTTTAAATTTTAAC[A/C/G]AACATTAACAAATGG	4703
rs116010361	snp	C/T	0.0197687	0.0974348	intron-variant	NEB, RIF1	GRCh38.p7	2:151502097	GATTGGAGACTAGTA[C/T]TGTAAGTGAAGTAAC	4703
rs116013237	snp	C/G	0.093777	0.195178	intron-variant	NEB, RIF1	GRCh38.p7	2:151509899	AGGCGCGAGCCACTG[C/G]GCCCGACCAAGAGTT	4703
rs116018925	snp	A/G	0.0138799	0.0821421	intron-variant	NEB	GRCh38.p7	2:151684177	TAACACCACTGAACT[A/G]TACACTTGAAAATTG	4703
rs116047847	snp	C/T	0.0577344	0.159793	intron-variant	NEB	GRCh38.p7	2:151694680	GTGATATGCATGTCA[C/T]GACCTTTAAAGACTA	4703
rs116145937	snp	A/T	0.00676609	0.0577691	intron-variant	NEB, RIF1	GRCh38.p7	2:151517044	ATGGAGCTTTATTTA[A/T]AAGTAAACAACTCTA	4703
rs116151533	snp	C/T	0.0138799	0.0821421	intron-variant	NEB	GRCh38.p7	2:151538296	TACCAAGTTAAATAA[C/T]TGAGCTCTTTTAAGC	4703
rs116155021	snp	A/T	0.00835141	0.0640778	intron-variant	NEB	GRCh38.p7	2:151680943	TTTCATGATTTTAAA[A/T]TGCAAAAACACTAGA	4703
rs116173761	snp	C/T	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151717035	TTTTTCCAAGTGTGA[C/T]GGATAAGATAGAACT	4703
rs116189169	snp	A/G	0.000934921	0.0216006	intron-variant	NEB	GRCh38.p7	2:151563817	AGAGGAAAAGGTCAT[A/G]CTGACCTCACTGTTC	4703
rs116203363	snp	C/T	0.00557542	0.0525036	intron-variant	NEB	GRCh38.p7	2:151543675	ATTGATTTTTAGAGA[C/T]GGGGTCTCACTATAT	4703
rs116216525	snp	A/G	0.093417	0.194889	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151498669	ACAAGGAGGGAAAAA[A/G]GTAGAAACAGACAAG	4703
rs116231664	snp	A/T	0.0111196	0.0737302	intron-variant	NEB	GRCh38.p7	2:151622502	TGCAAGAATGCTACA[A/T]TGAATACCAACTATC	4703
rs116233274	snp	C/T	0.00953873	0.0683987	intron-variant	NEB	GRCh38.p7	2:151684165	TGTTAATATACTTAA[C/T]ACCACTGAACTGTAC	4703
rs116270051	snp	C/T	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151682938	ATAGTAACAGCTCTT[C/T]GATTTTTGCTTTCCT	4703
rs116296071	snp	A/G	0.0916144	0.193427	intron-variant	NEB, RIF1	GRCh38.p7	2:151501731	AGTGGCTTGACTTAT[A/G]TAGGCCTTCTCTCAA	4703
rs116320537	snp	C/T	0.00517822	0.0506191	intron-variant	NEB	GRCh38.p7	2:151638569	TCAGAAGCTTTCTCA[C/T]AAATTTTCCAGAACG	4703
rs116340937	snp	C/T	0.00478085	0.0486577	intron-variant	NEB	GRCh38.p7	2:151643459	AAAGTTCATATTATA[C/T]TCTATATTTTTAATA	4703
rs116352209	snp	C/T	0.0337553	0.125452	intron-variant	NEB, RIF1	GRCh38.p7	2:151510015	TTTTAAGCTATATGT[C/T]TTTGTGTAAGTGTTC	4703
rs116352996	snp	A/C	0.00716266	0.059414	intron-variant	NEB, RIF1	GRCh38.p7	2:151523792	ATCAAACACTTGCCA[A/C]ACAAAATTTTAATGA	4703
rs116380444	snp	C/T	0.0410537	0.137264	intron-variant	NEB	GRCh38.p7	2:151626903	CTATACATTGGATAG[C/T]AATTTAATTGGATTT	4703
rs116381842	snp	A/G	0.0168055	0.0901129	intron-variant	NEB	GRCh38.p7	2:151635378	TGAGGCACCAGAAAA[A/G]GATGACAGTTTTGCT	4703
rs116443656	snp	A/G	0.00279162	0.0372561	utr-variant-3-prime, intron-variant	NEB, RIF1	GRCh38.p7	2:151485539	ATGTTTATAATGGAG[A/G]AAGACTCTAGGCACA	4703
rs116458746	snp	C/T	0.0364509	0.129988	intron-variant	NEB	GRCh38.p7	2:151621530	TATTATTTCATCAAC[C/T]GCTGCAAGTTGTTCG	4703
rs116459687	snp	A/G	0.0162398	0.0886349	intron-variant	NEB	GRCh38.p7	2:151675107	GTTATGTCCTTTAAA[A/G]TTGTCCTACATTTGA	4703
rs116482380	snp	A/G	0.00478085	0.0486577	intron-variant	NEB	GRCh38.p7	2:151554463	ACTCAGCAGGCTGAG[A/G]TGGGATGATTCCCGG	4703
rs116491855	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151723831	CTAACACAATGTAAG[A/G]AGCCAGGAAGCACTT	4703
rs116515133	snp	C/T	0.0165278	0.0893908	intron-variant	NEB	GRCh38.p7	2:151538113	AGTTGTAGAGCCCAA[C/T]ACAAGTAGAAATATT	4703
rs116533173	snp	A/G	1.65778e-05	0.002879	missense, intron-variant	NEB	GRCh38.p7	2:151614313	TTCCGAGCCTGAATG[A/G]CGTCATTCTGATCAG	4703
rs116533849	snp	A/T	0.0275645	0.114116	intron-variant	NEB, RIF1	GRCh38.p7	2:151520225	GTTAAATTAGGAGAA[A/T]TTATTGTTATTTTAA	4703
rs116545635	snp	A/G	0.0205511	0.0992634	intron-variant	NEB	GRCh38.p7	2:151626250	CTCCCAAGTACCTAA[A/G]ACTAGAGGTGCGTGT	4703
rs116550691	snp	G/T	0.0134861	0.0810011	intron-variant	NEB	GRCh38.p7	2:151613596	GTCCTATTATAGTTT[G/T]ATATAGTTTGGCTCT	4703
rs116551074	snp	A/G	0.0174175	0.0916809	intron-variant	NEB, RIF1	GRCh38.p7	2:151529521	TGACTATGGTCATCA[A/G]TGTTGCCATATAATT	4703
rs116553601	snp	A/G	0.0926964	0.194308	intron-variant	NEB, RIF1	GRCh38.p7	2:151520443	ATAAAAATAAGTTTA[A/G]GTAGGCAGAGGGCTA	4703
rs116565331	snp	C/T	0.00953873	0.0683987	intron-variant	NEB	GRCh38.p7	2:151706444	CTCTTAATAATTACA[C/T]AATTAGAAAGTCCTG	4703
rs116582799	snp	A/C	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151733914	GCCTCTACAGTTTGA[A/C]GCCAGAGAGTAAGAC	4703
rs116584331	snp	A/G	0.00398564	0.0444627	intron-variant	NEB	GRCh38.p7	2:151569544	GCGGCCAGGCAGTGT[A/G]ACAAACGATAGCATA	4703
rs116609336	snp	A/G	0.0103295	0.0711199	intron-variant	NEB	GRCh38.p7	2:151660812	CTCTGTTTTAGACCA[A/G]CACTATACAATAGAA	4703
rs116629550	snp	C/T	0.00438332	0.0466095	intron-variant	NEB	GRCh38.p7	2:151715154	CTGTCACCTTGCCCA[C/T]CTAGAGTGGTGCCAT	4703
rs116645787	snp	G/T	0.112631	0.208878	intron-variant	NEB, RIF1	GRCh38.p7	2:151508628	GGACTGAGCCGGCAG[G/T]CAGACAGGCAGGCCC	4703
rs116658949	snp	C/T	0.0115144	0.0749975	intron-variant	NEB	GRCh38.p7	2:151652480	TCTTCCTGCCTTGGC[C/T]TCCCAAAGTGCTGAG	4703
rs116662255	snp	C/T	0.0581099	0.160244	intron-variant	NEB	GRCh38.p7	2:151646758	GAGTTCAAGTGATTC[C/T]GGTGCCTCAGCCACC	4703
rs116667161	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151663272	TAGACATATTCCTTT[C/T]AATACACTCTTTCTG	4703
rs116670236	snp	A/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151507163	AGCCCAAGGGAAATT[A/T]TTTGATAAGAATTTT	4703
rs116671455	snp	A/G	0.0825414	0.185628	intron-variant	NEB	GRCh38.p7	2:151574825	CAGCCTCTTCCTCCT[A/G]GGCTCAAGTGATCCT	4703
rs116678485	snp	A/C/T	0.000135025	0.00821561	missense	NEB	GRCh38.p7	2:151724274	CCTTGCTGAACATGG[A/C/T]GGTGTTCTTAACGGC	4703
rs116692677	snp	C/G	0.00676609	0.0577691	intron-variant	NEB	GRCh38.p7	2:151534883	TACTGAAAGTGAACT[C/G]AATCAAATGTAAAGA	4703
rs116694552	snp	C/T	0.0119091	0.0762411	intron-variant	NEB	GRCh38.p7	2:151632943	ACAGGGTTCTGTATG[C/T]CAGAAGCTACAGAAC	4703
rs116698898	snp	A/T	0.00099802	0.0223162	intron-variant	NEB, RIF1	GRCh38.p7	2:151505432	CCAGGGTAGCAATTG[A/T]GAGATGGCCAGTCAC	4703
rs116719754	snp	A/T	0.0228947	0.104514	intron-variant	NEB	GRCh38.p7	2:151723821	CTTACAAGTGCTAAC[A/T]CAATGTAAGGAGCCA	4703
rs116755797	snp	A/G	0.00557542	0.0525036	intron-variant	NEB, RIF1	GRCh38.p7	2:151528547	CCATCCTCAGGATAC[A/G]TACAAGCTCTTTGCC	4703
rs116777627	snp	C/T	0.00358779	0.0422022	intron-variant	NEB	GRCh38.p7	2:151687979	TGCTGTCCTGATTTA[C/T]ATAAGGATGCTATAA	4703
rs116828574	snp	C/G	0.00835141	0.0640778	intron-variant	NEB	GRCh38.p7	2:151731578	TTTCTGGCAGGCAGT[C/G]TATTCGTTTATCACC	4703
rs116830087	snp	C/T	0.0142736	0.0832652	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151495234	CTCCCCTCAGTGTCA[C/T]TCTTGGAAACGTGGG	4703
rs116847832	snp	C/T	0.0352966	0.128072	intron-variant	NEB	GRCh38.p7	2:151616354	AAATCAACATTTGGT[C/T]GGCAAAATTTTATTT	4703
rs116894469	snp	C/T	0.040671	0.13668	intron-variant	NEB	GRCh38.p7	2:151613526	AGCAATATATTACAG[C/T]AGTATTGACACTACA	4703
rs116897114	snp	G/T	0.0221141	0.102801	intron-variant	NEB, RIF1	GRCh38.p7	2:151503724	TACCAATGAGAAAAA[G/T]CTAACCATTTTGTTG	4703
rs116903097	snp	A/T	0.00601566	0.0545128	intron-variant	NEB	GRCh38.p7	2:151674466	AAACTTCACCTAAAA[A/T]TTGTACTCACATCAC	4703
rs116980949	snp	A/G	0.0228947	0.104514	intron-variant	NEB, RIF1	GRCh38.p7	2:151531667	ATAACAGGACATCTC[A/G]CACCCCTGCCTCCCT	4703
rs117018177	snp	C/T	0.0113199	0.0743762	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151618347	ACTGGTAAATTTCAG[C/T]GTTTCTGGACGCTGA	4703
rs117036376	snp	A/G	0.012547	0.0782053	intron-variant	NEB	GRCh38.p7	2:151630860	TAAAAATCATTTGAA[A/G]TAGAAATGACAAAAA	4703
rs117048449	snp	C/T	0.0161553	0.0884118	NEB	2	allele_origin=T(germline)/C(germline)	2:151678031	TATCATGGGGCGTGT[C/T]GTATTTGGACTTTGT	4703
rs117052683	snp	A/G	0.030278	0.119257	intron-variant	NEB	GRCh38.p7	2:151620107	GGGGCGTATGTTTAC[A/G]TGGATCATTAAAATT	4703
rs117071114	snp	C/T	0.0228947	0.104514	intron-variant	NEB	GRCh38.p7	2:151540920	TGCTTACTGTCCTGA[C/T]GTTTGTTTGCTTGTT	4703
rs117101614	snp	C/T	0.039522	0.134904	intron-variant	NEB	GRCh38.p7	2:151651590	GAGCTCAACATACTG[C/T]CAAATGGGTCAAAAT	4703
rs117126164	snp	A/G	0.00358779	0.0422022	intron-variant	NEB	GRCh38.p7	2:151612857	TTTGGGGATAAAAAC[A/G]ACGTCTTTTTCGTAT	4703
rs117151886	snp	C/G	0.00159617	0.0282053	intron-variant	NEB, RIF1	GRCh38.p7	2:151508400	CCACAGGAGGAAGGT[C/G]ACAGCCAGCAAGGCC	4703
rs117178114	snp	A/G	0.00364667	0.0425445	synonymous-codon	NEB	GRCh38.p7	2:151733145	CTCCTCATAGTCTTC[A/G]TCATCTGCCATTTTT	4703
rs117179677	snp	A/C	0.0271762	0.113356	intron-variant	NEB	GRCh38.p7	2:151613542	AGTATTGACACTACA[A/C]CTGACTTTGTCAGCT	4703
rs117212662	snp	A/G	0.00597247	0.0543191	intron-variant	NEB	GRCh38.p7	2:151715481	ACTTGAAGGTAAGGG[A/G]ATTTGGGAAGCAATT	4703
rs117227069	snp	C/T	0.0228947	0.104514	intron-variant	NEB, RIF1	GRCh38.p7	2:151492591	GGAGCTGGTGAGGGA[C/T]GCTTGGGTCAACTGA	4703
rs117240999	snp	A/C	0.0310518	0.120672	intron-variant	NEB	GRCh38.p7	2:151722430	TACCAAAATTCCGGC[A/C]AGTGGGATCACTGAT	4703
rs117255929	snp	A/G	0.0368353	0.130617	intron-variant	NEB	GRCh38.p7	2:151645287	ATGGGGAAAAATCAT[A/G]CCTAAGGGGTTATCT	4703
rs117256095	snp	A/C	0.0225045	0.103662	intron-variant	NEB, RIF1	GRCh38.p7	2:151523692	AACTGGGTTTGGGCA[A/C]CACATTTCTGAGTCC	4703
rs117270796	snp	C/T	0.0184235	0.0941931	intron-variant	NEB	GRCh38.p7	2:151625525	AAGAAATAAAACAAA[C/T]GATCTTACCTCACTA	4703
rs117271684	snp	A/G	0.0176915	0.092373	NEB	2	allele_origin=G(germline)/A(germline)	2:151665469	TTCTTTGCCTTCTCC[A/G]CCTCCAGGGACTCTA	4703
rs117299707	snp	C/T	0.0376037	0.131863	intron-variant	NEB	GRCh38.p7	2:151666953	AGCCCTAATACAAAT[C/T]AGTGTATTAATCTTG	4703
rs117339427	snp	C/T	0.00835141	0.0640778	intron-variant	NEB	GRCh38.p7	2:151540000	ACAGCAGGCAAGTAA[C/T]AGCATCAGGATTTGA	4703
rs117353554	snp	C/G	0.0337553	0.125452	intron-variant	NEB	GRCh38.p7	2:151660037	AAGGACCTGATTCCC[C/G]AACTTTTGGCAAATA	4703
rs117356356	snp	C/T	0.029116	0.117091	intron-variant	NEB	GRCh38.p7	2:151728064	ATGGCACACTGTAGC[C/T]GTATGAAGGCACATT	4703
rs117361266	snp	C/T	0.0271762	0.113356	intron-variant	NEB	GRCh38.p7	2:151620581	TGGGGCAAACTCAGT[C/T]AAGCCTGCTTCTTTT	4703
rs117363062	snp	C/T	0.0379877	0.132479	intron-variant	NEB	GRCh38.p7	2:151662668	CAGGTGACTGTTATC[C/T]CCTTGAGAAAAGCAA	4703
rs117367844	snp	C/T	0.0225045	0.103662	intron-variant	NEB, RIF1	GRCh38.p7	2:151519468	GAGGTTCCCAGGAGC[C/T]GACGGGAGGAGGGAA	4703
rs117379193	snp	C/T	0.0267878	0.112589	intron-variant	NEB	GRCh38.p7	2:151669240	TGTGTTTTCCATTTA[C/T]GAGACAAATACCTAC	4703
rs117383372	snp	A/C	0.0178098	0.0926698	intron-variant	NEB	GRCh38.p7	2:151642111	TCCATCTTTTAAAGA[A/C]AGCAAATATTTGTAA	4703
rs117405908	snp	A/G	0.0240643	0.107019	intron-variant	NEB	GRCh38.p7	2:151578904	CTGGCCAAGATGGCA[A/G]AGACCTGTCTCTAAT	4703
rs117455474	snp	A/T	0.0287284	0.116357	intron-variant	NEB	GRCh38.p7	2:151733422	ATAATCAGTTTAGTT[A/T]AAATTGTAAAACGAA	4703
rs117457833	snp	C/G	0.0123036	0.0774623	intron-variant	NEB	GRCh38.p7	2:151545045	CCAATCATCAAGGAA[C/G]CAACACTCTAGGTGA	4703
rs117526319	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151528820	GCACCAAATGGCTCA[A/G]TGTTTTCTTCATCAG	4703
rs117543436	snp	C/T	0.0225045	0.103662	intron-variant	NEB, RIF1	GRCh38.p7	2:151508826	CTTTGGCTGGAGAGA[C/T]GTGTCCATATAGAGG	4703
rs117602829	snp	A/T	0.0329836	0.124112	intron-variant	NEB	GRCh38.p7	2:151719448	TTTATACTTTAACCA[A/T]GTCTAACTGTATCTT	4703
rs117632493	snp	A/C	0.0154538	0.0865337	intron-variant	NEB, RIF1	GRCh38.p7	2:151490199	TCCAAAAAGAGAAAT[A/C]AAAGAAAATGAAACA	4703
rs117636679	snp	C/G	0.000629045	0.0177236	missense, intron-variant	NEB	GRCh38.p7	2:151627640	TAAGGTCTGGCACTT[C/G]TTGGCTAACACCACT	4703
rs117652649	snp	A/G	0.0228947	0.104514	intron-variant	NEB, RIF1	GRCh38.p7	2:151507786	TATATTTTCTCCCCA[A/G]TACCACCAACGAAGT	4703
rs117655716	snp	A/G	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151669293	GGTAGATGCATTTAT[A/G]TTCCCATTCTACCAG	4703
rs117694074	snp	C/G	0.00990481	0.0696728	intron-variant	NEB, RIF1	GRCh38.p7	2:151513537	ATGTCCTTAAAGTTA[C/G]AACTACTTTCCTGAA	4703
rs117699521	snp	C/T	0.0225045	0.103662	intron-variant	NEB, RIF1	GRCh38.p7	2:151515034	TCTATGTATGGGCTC[C/T]TAATCATAGTTCTGC	4703
rs117720056	snp	A/G	0.0376037	0.131863	intron-variant	NEB	GRCh38.p7	2:151665635	AAAAGAAAAAGAGAA[A/G]CTGGGAGGGGGAGAA	4703
rs117726863	snp	A/G	0.0368353	0.130617	intron-variant	NEB	GRCh38.p7	2:151662983	TTTCGTCTGCTTTGG[A/G]TTTGTAACTTAATTC	4703
rs117763518	snp	C/T	0.00279162	0.0372561	intron-variant	NEB	GRCh38.p7	2:151539877	CAGCAGCATGCTAGA[C/T]ACTTATACATTATCT	4703
rs117769877	snp	C/T	0.0287284	0.116357	upstream-variant-2KB	NEB	GRCh38.p7	2:151735676	GCCGAGGCGGGCAGA[C/T]TGTCTGAGGCCAGGA	4703
rs117784928	snp	A/G	0.0221141	0.102801	intron-variant	NEB, RIF1	GRCh38.p7	2:151518128	CATAATTGCATGTAT[A/G]TTTCTCAACTATATG	4703
rs117787020	snp	C/T	0.0225045	0.103662	intron-variant	NEB	GRCh38.p7	2:151707674	TCAGGAGCCTGTCCA[C/T]AGGGATTAGAACAAG	4703
rs117821421	snp	C/T	0.0267878	0.112589	intron-variant	NEB	GRCh38.p7	2:151561754	TTTCCAGATACTGAT[C/T]TTTTTCCTCCAAAAC	4703
rs117861109	snp	C/T	0.000687475	0.0185274	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151485774	CCTAAATAGCTTCAA[C/T]GTAGTTGGCTGGGAG	4703
rs117862553	snp	G/T	0.0916144	0.193427	intron-variant	NEB, RIF1	GRCh38.p7	2:151494634	TACATCAGCTGTTTG[G/T]TTTTTTTTGTTTTGT	4703
rs117864132	snp	C/T	0.039522	0.134904	intron-variant	NEB	GRCh38.p7	2:151647515	GGTTACTCAACAGTA[C/T]AGCAACCTGGCACCA	4703
rs117900257	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151730722	GAAAACATTAAGATG[C/T]AAAATTTCCCTCAAT	4703
rs117911815	snp	A/G	0.0287284	0.116357	intron-variant	NEB	GRCh38.p7	2:151719697	CAGCCAGGGCAATAC[A/G]GTGAAACCCTGTCTC	4703
rs117959904	snp	A/G	0.00954707	0.068428	intron-variant	NEB, RIF1	GRCh38.p7	2:151518280	TTGTACTGTGGATGA[A/G]TGTGCGCCAGAGGAA	4703
rs117976261	snp	C/T	0.0165278	0.0893908	intron-variant	NEB	GRCh38.p7	2:151561827	TGCAAGTTAACTTGA[C/T]CAACTAAGGTACAGA	4703
rs117987498	snp	C/T	0.0287284	0.116357	intron-variant	NEB	GRCh38.p7	2:151729169	ATGCATCATCAGGGA[C/T]GAAGCCCTGGAGACA	4703
rs118012311	snp	C/T	0.00279162	0.0372561	intron-variant	NEB	GRCh38.p7	2:151566600	AAGTAGAGATCTTGA[C/T]TCAGGCTTCAGTGGG	4703
rs118023496	snp	C/T	0.0225045	0.103662	intron-variant	NEB	GRCh38.p7	2:151561719	CTGCCCTATCAGAGC[C/T]GAACCACGTGCTGAA	4703
rs118047174	snp	A/G	0.0368353	0.130617	intron-variant	NEB	GRCh38.p7	2:151679543	TAGAAGGTTATACAA[A/G]TCTTTTCCCTCCAGA	4703
rs118093256	snp	C/G	0.0577344	0.159793	intron-variant	NEB	GRCh38.p7	2:151622628	TGTTGAACTGATTAA[C/G]AGAAAATTGTACACA	4703
rs118100369	snp	A/G	0.00953873	0.0683987	intron-variant	NEB	GRCh38.p7	2:151732110	AATTTGGTTCTGGGT[A/G]GCTCTTACAGTTAAT	4703
rs118135772	snp	C/T	0.00358779	0.0422022	intron-variant	NEB	GRCh38.p7	2:151709598	ATACAAGAGCCAAAG[C/T]TATAAGAAATTTACC	4703
rs118137536	snp	A/G	0.0930568	0.194599	intron-variant	NEB, RIF1	GRCh38.p7	2:151521893	CTTCTTAAAACTAGT[A/G]TAGTTTGAAAGGTAA	4703
rs118148087	snp	C/T	0.0402882	0.136092	intron-variant	NEB	GRCh38.p7	2:151678790	ACATGAGGGAAGGTT[C/T]GTGGAAAGTTGGGGC	4703
rs118159416	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151653749	CTTTGTAACATCTCC[A/G]AGTAGAGCATCTTAC	4703
rs118191309	snp	G/T	0.00953034	0.0683692	missense, nc-transcript-variant, intron-variant	NEB, RIF1	GRCh38.p7	2:151506216	TCATCTCAGGTGTCT[G/T]TCCGATAGCCGTTCC	4703
rs121913662	snp	A/G/T	0.000130967	0.00809113	NEB, RIF1	2	allele_origin=G(germline)/T(germline)	2:151490495	CAGCGCCGGAGCCGG[A/G/T]AGCAGTCACGATCTG	4703
rs137861708	snp	C/T	0.000830974	0.0203666	intron-variant	NEB	GRCh38.p7	2:151688255	TTTTCTCTTTTCATG[C/T]ACACCAAACATAGGC	4703
rs137862068	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151640896	ACTTTAATACATTCT[C/T]TAATGTGAAAGTCAT	4703
rs137863488	snp	G/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151612824	TTACTGGTTGATCAC[G/T]TTGCATTAATGTGTT	4703
rs137932054	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151500903	CACGCCTGGCCCCAA[A/G]TAAGATTTCTTTTGG	4703
rs137934821	snp	A/G	6.76049e-05	0.00581359	intron-variant	NEB	GRCh38.p7	2:151552784	TACTTGATCTGCCGA[A/G]AGGAAGAAAACAAGC	4703
rs137945369	snp	G/T	0.00318978	0.0398085	intron-variant	NEB	GRCh38.p7	2:151543005	CTGTCTTTCCTGCCT[G/T]GAATGTTCTTCTCCC	4703
rs137948760	snp	C/T	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151645416	AATTTCTAAAACTTA[C/T]GTTTTGAAGAAGGTT	4703
rs137949406	snp	C/T	1.70592e-05	0.0029205	missense, intron-variant	NEB	GRCh38.p7	2:151609858	ATAATGTCGTTTTGA[C/T]CCGGCATGCATGTCC	4703
rs137985656	snp	C/T	0.00557542	0.0525036	intron-variant, utr-variant-3-prime, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151497939	GGGCTGTCAGAGTTA[C/T]CCATGTTATTTTTTT	4703
rs137991128	snp	A/C	0.0103295	0.0711199	intron-variant	NEB	GRCh38.p7	2:151675508	AAAAATCATCAAAGG[A/C]ATTTTCCTATTTTTT	4703
rs138032453	snp	A/G	0.00398564	0.0444627	intron-variant	NEB, RIF1	GRCh38.p7	2:151530702	TGTCTCGTCTACACA[A/G]TAGCCCAGCTCCCAG	4703
rs138036522	snp	C/T	0.00557542	0.0525036	intron-variant	NEB	GRCh38.p7	2:151710766	ACTAACGCCCCCTCC[C/T]CTTGCTGAGTTTGGG	4703
rs138054267	snp	C/T	0.0174175	0.0916809	intron-variant	NEB	GRCh38.p7	2:151577909	CTTCTTCTTTATTCA[C/T]CATGGTATCTTTAGT	4703
rs138055952	snp	C/G	0.0260105	0.111035	intron-variant	NEB, RIF1	GRCh38.p7	2:151494784	CTCCTGAGTAGCTGG[C/G]ATTACAGGCGTGCAC	4703
rs138058093	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151680638	GGGTCTCTTCATATT[A/G]TATAATAACTAGAGG	4703
rs138059383	snp	A/G	0.000223219	0.0105622	intron-variant	NEB	GRCh38.p7	2:151547576	TATGTATTAGAGACC[A/G]AATGATTAACATTCA	4703
rs138059770	snp	C/T	0.00676609	0.0577691	intron-variant	NEB	GRCh38.p7	2:151625765	ATGTATGTTAATATT[C/T]TTTTCAACCTCTTTG	4703
rs138072848	snp	A/G	0.0150606	0.0854603	intron-variant	NEB	GRCh38.p7	2:151635807	ATTTCAATAGCAAGC[A/G]CCGCATGTGTTTTAA	4703
rs138123589	snp	A/G	0.0448719	0.142907	intron-variant	NEB	GRCh38.p7	2:151702384	ATGTCAATTAGGTCC[A/G]CTTGGTGCAGAGCTG	4703
rs138144648	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151567060	CTTTGGGAACAAATT[A/G]AATATCGATGGCCTC	4703
rs138169600	snp	C/G	0.00318978	0.0398085	intron-variant	NEB	GRCh38.p7	2:151635391	AAGGATGACAGTTTT[C/G]CTCTGGGAGACGTGC	4703
rs138175434	snp	A/G	0.00318978	0.0398085	intron-variant	NEB	GRCh38.p7	2:151669561	GAGAGAGGGGCAGAG[A/G]AAGAGCATTCGGGAC	4703
rs138175786	snp	A/T	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151624614	TTTTAAGGCTACATT[A/T]TTATAGGCAAAAGTA	4703
rs138178619	snp	C/T	0.00358779	0.0422022	intron-variant	NEB, RIF1	GRCh38.p7	2:151487850	TTAAACTCCTGGACT[C/T]AAGCAGTCCTCCCAC	4703
rs138201194	snp	C/G	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151656770	AGATTTTGTGATGAT[C/G]CATCACACTGACTTA	4703
rs138217855	snp	C/T	0.00125683	0.0250367	missense, intron-variant	NEB	GRCh38.p7	2:151639296	TCACTGTAGTTGATT[C/T]TGTTCATTCTTGCCA	4703
rs138217960	snp	C/T	0.00440739	0.0467362	missense	NEB	GRCh38.p7	2:151567437	TCGTCGGGACACCAA[C/T]ATAATGACCTTTTTG	4703
rs138264765	snp	A/T	0.0123036	0.0774623	intron-variant	NEB	GRCh38.p7	2:151666453	CATAGAAGTCTGATA[A/T]AAACTGAATTTATAC	4703
rs138272049	snp	C/G/T	0.00358779	0.0422022	intron-variant	NEB	GRCh38.p7	2:151562037	ACTTTCTTTGCCTGC[C/G/T]CATCAGCCCACTGAC	4703
rs138288574	snp	C/T	9.94448e-05	0.00705071	intron-variant	NEB, RIF1	GRCh38.p7	2:151526114	CATCTGCCTGGGGCG[C/T]TCTCCCAAGAGGGAA	4703
rs138315391	snp	C/T	0.00438332	0.0466095	intron-variant	NEB	GRCh38.p7	2:151651061	AGTAGCTGGGATTTA[C/T]AGGTACATGCCACCT	4703
rs138326210	snp	A/G	0.00676609	0.0577691	intron-variant	NEB, RIF1	GRCh38.p7	2:151530040	AGCTATTATCATATC[A/G]TGTTATAATTTTTTT	4703
rs138329241	snp	A/G	0.0023933	0.0345097	intron-variant	NEB, RIF1	GRCh38.p7	2:151520335	AGTTTGGGGGTTAAT[A/G]GCTTCAAGTGTGATT	4703
rs138333783	snp	A/G	0.00438332	0.0466095	intron-variant	NEB, RIF1	GRCh38.p7	2:151514548	GTTTAGTAAGTAAAA[A/G]TATGAATACAGGCAG	4703
rs138339671	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151628415	TGAGGTTTGTTTGGG[A/G]TTCCTCAAGTGAAAA	4703
rs138381510	snp	C/T	0.0023933	0.0345097	upstream-variant-2KB	NEB	GRCh38.p7	2:151735635	GGGCGTGGTGGCTCA[C/T]GCCTGTAATCCCAAC	4703
rs138410068	snp	A/G	0.0209421	0.100162	intron-variant	NEB	GRCh38.p7	2:151544571	CAGGATAAAAATAAC[A/G]TAAGCGTTCTAGTCT	4703
rs138430810	snp	C/T	0.00358779	0.0422022	intron-variant	NEB	GRCh38.p7	2:151684368	TTTCTTTTCAGATAG[C/T]AATCTATGTAAAAAT	4703
rs138442208	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151619221	CTGAATCCCTAGGAA[A/G]ATTTATACCTGTTTA	4703
rs138447923	snp	A/G	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151694248	TTCAGTTAGGCTAAC[A/G]TCCATCCAAGGTTAT	4703
rs138505166	snp	C/T	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151578035	AAACTGTCTTAAATA[C/T]ACCACTTGGCAATGC	4703
rs138505318	snp	C/T	0.00478085	0.0486577	intron-variant	NEB	GRCh38.p7	2:151650476	ATGCATTTTAGATTT[C/T]CAATAATAATTCCTA	4703
rs138509965	snp	C/T	0.00358779	0.0422022	intron-variant	NEB	GRCh38.p7	2:151728060	GGAAATGGCACACTG[C/T]AGCCGTATGAAGGCA	4703
rs138524588	snp	C/G	0.00597247	0.0543191	intron-variant	NEB	GRCh38.p7	2:151697035	AAATAGACTTCATTT[C/G]TTGCGATTGCCTGGC	4703
rs138528093	snp	C/T	0.00215685	0.0327684	synonymous-codon	NEB	GRCh38.p7	2:151723424	AACTCTCCTCAGTTC[C/T]GGGCTATCATTATAG	4703
rs138558301	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151623064	CTGATTTACTTAAAA[C/T]GATCCATGCCAGTTT	4703
rs138566719	snp	A/C	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151504350	ACTCTTCACCCAACA[A/C]AGCAGCAGAATTGAT	4703
rs138582547	snp	C/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151488270	TTGTTATAGAAACAT[C/T]TAAAATTTTATGATC	4703
rs138602456	snp	A/G	0.0138799	0.0821421	intron-variant	NEB	GRCh38.p7	2:151608955	TGTCAACATTTAATG[A/G]AAAAATTGGCAAAGA	4703
rs138605836	snp	A/G	0.00517822	0.0506191	intron-variant	NEB	GRCh38.p7	2:151534983	TACTAATTTTCTCAC[A/G]GAATTTTTGAACTTA	4703
rs138684936	snp	A/C	0.123105	0.215401	intron-variant	NEB, RIF1	GRCh38.p7	2:151510060	ATAAGTGATTAACTT[A/C]TTTTAATTTATAACT	4703
rs138685043	in-del	-/CTTGT	0.0240643	0.107019	intron-variant	NEB	GRCh38.p7	2:151688212	TTATTTGCACAATTC[-/CTTGT]CTTGTCTTTTAAAAT	4703
rs138713770	snp	C/T	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151714222	AATTCCCTCTGACCC[C/T]TTCCCTGAGTTTTCA	4703
rs138720541	in-del	-/AACAA			intron-variant	NEB	GRCh38.p7	2:151698083	ACAAAACAAAACAAA[-/AACAA]ACAAAACAAAACAAA	4703
rs138747940	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151673874	TAGCAGCTGGGACTA[C/T]AGGTGCCCGCCACCA	4703
rs138787956	snp	A/C/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151674927	TCAAGAGAAGACCTG[A/C/G]TGGTCAGCTTTAGAA	4703
rs138789068	snp	A/T	0.00279162	0.0372561	intron-variant	NEB	GRCh38.p7	2:151560333	CTAGCAGAGATTATC[A/T]TGTGCAGACAGGCAG	4703
rs138792610	snp	A/T	0.0271762	0.113356	intron-variant	NEB	GRCh38.p7	2:151709573	ACTCCTCCCCTTTTT[A/T]ACTAATTATATACAA	4703
rs138809126	in-del	-/TTTA	0.491047	0.066306	intron-variant	NEB	GRCh38.p7	2:151574722	GTCTACAGTTTAAAT[-/TTTA]TTTATTTATTTATTT	4703
rs138829987	in-del	-/A	0.0337553	0.125452	intron-variant	NEB	GRCh38.p7	2:151654802	ATACATCTCAAAAAT[-/A]GGCAAAGCCAAAACT	4703
rs138833499	snp	C/T	0.0111196	0.0737302	intron-variant	NEB	GRCh38.p7	2:151629370	AGATACTGAAGTCTT[C/T]CGAAGCTTAAAACAT	4703
rs138875082	snp	C/G	0.00199481	0.0315187	upstream-variant-2KB	NEB	GRCh38.p7	2:151734668	AATTTTACCTAACTT[C/G]CAGCCTGTGCAGTTC	4703
rs138875496	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151718386	ATACTCTATGACCCT[A/G]TGGTATACTAATGCC	4703
rs138944369	snp	A/G	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151577341	CCTGTCTTTCAATTC[A/G]TAGTCTCATCAGCCC	4703
rs138947072	snp	A/G	0.00199481	0.0315187	intron-variant	NEB, RIF1	GRCh38.p7	2:151526722	GAGGACTGTCACCTG[A/G]ATCTAATGGCCCTTG	4703
rs138951514	snp	A/C	0.0142736	0.0832652	intron-variant	NEB	GRCh38.p7	2:151679115	ACCTCGGAGACTCCA[A/C]AGAAATCATGGGGAG	4703
rs138954717	snp	C/G	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151613705	CCCCTTGCTGTTCTT[C/G]TGATAGTGAGTGAAT	4703
rs138956213	snp	A/T	0.0225045	0.103662	intron-variant	NEB, RIF1	GRCh38.p7	2:151520018	AGGTATAAAAAGTAA[A/T]CACCTCTTTCTAATG	4703
rs138976590	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151566376	AAGAAGAGTTGCTAT[G/T]CTGATTTAAGTTCCA	4703
rs138997554	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151568836	CCGTATTTGAATAGC[A/G]TCTTCTTGGGAATTT	4703
rs139042849	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151715032	GGAATAAATAATGTC[A/T]CCATGGCCAAATCCA	4703
rs139046315	snp	A/G	0.0232847	0.105357	intron-variant	NEB	GRCh38.p7	2:151536151	GGGCTCAGGCTATCC[A/G]CCTGCCTTGGCCTCC	4703
rs139063222	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151637079	GTGCGGGGTACTTGG[A/G]AATCAAAGATGAGGT	4703
rs139106679	snp	A/G	0.0130921	0.0798413	intron-variant	NEB	GRCh38.p7	2:151705107	TAAGGTGAGAAATAC[A/G]CAATCTCCCTCCCTC	4703
rs139125293	snp	C/T	6.62427e-05	0.00575473	missense	NEB	GRCh38.p7	2:151694390	TTAATGCTGAGGACT[C/T]CAATCATTTTCCCTT	4703
rs139127912	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151666854	CGTGTGAGCCACCAT[G/T]TCTGGTCAATGTATG	4703
rs139136694	snp	C/T	0.0228947	0.104514	intron-variant	NEB, RIF1	GRCh38.p7	2:151531678	TCTCGCACCCCTGCC[C/T]CCCTCCCACTAAATG	4703
rs139193329	snp	A/G	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151653729	AAAACTTGCAATCTC[A/G]GGTCCTTTGTAACAT	4703
rs139196646	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151731948	AGGCTGAGTGTTACA[C/T]TGTACGAGATTCATT	4703
rs139201963	snp	A/T	0.0302489	0.119203	intron-variant	NEB	GRCh38.p7	2:151655249	ATACAAAACTTAAAA[A/T]TAATTTTTATATAAA	4703
rs139207731	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151517284	AAACAGGCGAAGACC[C/T]TCATGCACGCAGCAC	4703
rs139216819	snp	A/G	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151488540	AGTCCTAGCTATTCT[A/G]GTGGCTGAGGCTGGA	4703
rs139240018	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151553287	CTTTCTCCAGCTCAG[A/C]CACCCCCCAGAGCTG	4703
rs139249092	in-del	-/ATAA	0.497182	0.037434	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151499031	ATTTGCCAAAGCAGT[-/ATAA]ATAAATGTGGATGCT	4703
rs139266987	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151621217	AAAATTTCACATTCA[A/G]CAAGTTTTAACATCA	4703
rs139277072	snp	C/T	0.00358779	0.0422022	intron-variant	NEB	GRCh38.p7	2:151695824	AGGCCATCTGCATTA[C/T]TGATCCTGTGTGCAG	4703
rs139290927	snp	A/G	0.0287284	0.116357	intron-variant	NEB	GRCh38.p7	2:151698088	AACAAAACAAAACAA[A/G]ACAAAACAAAAAGAA	4703
rs139318997	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151553634	TTATGCAAAGAGGCT[A/C]AGGGGAGCCACAGAA	4703
rs139333406	snp	C/T	0.000287283	0.0119816	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151490506	TGCTCCCGGCTCCGG[C/T]GCTGAGCTTGGACTG	4703
rs139367082	snp	C/G	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151558067	TCAATTAGGAAAAGA[C/G]GAAGTCAAATTGTCT	4703
rs139367179	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151505731	CTCATTCTGATACTG[A/G]GTAAGAGGAGAACAA	4703
rs139370581	snp	A/T	0.0174175	0.0916809	intron-variant	NEB	GRCh38.p7	2:151659297	TTAAATTAATTAATT[A/T]ATTTATTTATTATTT	4703
rs139376582	snp	G/T	0.0209421	0.100162	intron-variant	NEB, RIF1	GRCh38.p7	2:151506074	AATATAAGCTGTTTC[G/T]GGTGACAGAGGCTTT	4703
rs139386074	snp	A/G	0.00914312	0.0669923	intron-variant	NEB	GRCh38.p7	2:151625199	GAAAATAAACTTGCC[A/G]CACAAATTTTGAAGC	4703
rs139390050	snp	C/T	0.00478085	0.0486577	intron-variant	NEB	GRCh38.p7	2:151551628	TTCACCTCATGTGAA[C/T]AGAACAGCATTTATA	4703
rs139419111	snp	C/T	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151671773	GAGCAATATTTTTAT[C/T]GAGTGCCAATAAATG	4703
rs139444150	snp	A/G	0.0154538	0.0865337	intron-variant	NEB	GRCh38.p7	2:151634159	TCATGTAATTGTAGT[A/G]TATACCCCAAATCAC	4703
rs139461481	snp	A/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151667972	AGGAATGAAACAGAA[A/T]GCCAAAATGTTTCTT	4703
rs139463983	snp	G/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151676547	TAAAAATTAGCATAC[G/T]AGTCCCTTACTAATC	4703
rs139512360	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151516853	GCTGATGCAAGAAAA[C/T]GCATGGGGAAAATTA	4703
rs139537041	snp	C/T	0.00358779	0.0422022	intron-variant	NEB	GRCh38.p7	2:151629879	TATATTAACCTATTA[C/T]ATATCATTATAGATT	4703
rs139546341	snp	A/T	0.00478085	0.0486577	intron-variant	NEB	GRCh38.p7	2:151572703	GGTGAGCCACCACTA[A/T]GCCTGGCTATTTTTT	4703
rs139548236	snp	A/G	0.00318978	0.0398085	intron-variant	NEB, RIF1	GRCh38.p7	2:151511846	ATTGGTAATCCAAAT[A/G]TGGGCTACTTTGTTT	4703
rs139548702	snp	C/T	0.000331373	0.0128677	missense, intron-variant	NEB	GRCh38.p7	2:151629627	TTTTTTGCTTCTTCA[C/T]TGGCAAGTTTGTATA	4703
rs139553563	snp	A/G	0.00636936	0.0560724	intron-variant	NEB	GRCh38.p7	2:151708008	ACTCTCCCCCTACCC[A/G]CATCTGGGATACACA	4703
rs139564587	snp	A/G	3.53526e-05	0.00420417	intron-variant	NEB	GRCh38.p7	2:151619779	TGAAAGAGAGAATCC[A/G]GTAAATAAGAAGGAA	4703
rs139583928	snp	C/T	0.00597247	0.0543191	intron-variant	NEB, RIF1	GRCh38.p7	2:151522844	ATTCCGCCTAGAGTA[C/T]GCAGCAAGACAGCAA	4703
rs139616481	snp	C/T	0.0060785	0.0547933	intron-variant	NEB	GRCh38.p7	2:151690862	AATGAAATATCAGTA[C/T]ATTCTTGGTTATACA	4703
rs139622158	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151698341	CACCACAATCAATTT[G/T]AAAACATTTCATCAT	4703
rs139636644	snp	G/T	0.0117027	0.0755936	missense	NEB	GRCh38.p7	2:151560620	TGCTTCTGGTTCTTG[G/T]CGTGTGTCAGGGACA	4703
rs139657051	snp	A/G	0.00279162	0.0372561	intron-variant	NEB	GRCh38.p7	2:151574663	TATCATTTTAATGTA[A/G]TGCTGAATTTGATTT	4703
rs139682001	in-del	-/TA			intron-variant	NEB	GRCh38.p7	2:151562955	ATATTCTTTATACTT[-/TA]TATATATATACTTTA	4703
rs139697701	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151527689	AAAACATCTCAAATC[A/G]TGATTCCTAATGCAA	4703
rs139707348	snp	C/T	0.00318978	0.0398085	intron-variant	NEB	GRCh38.p7	2:151633182	CATGTGGCTCCTCCA[C/T]AGACAGCCAGGCTAA	4703
rs139749127	snp	G/T	0.00358779	0.0422022	intron-variant	NEB	GRCh38.p7	2:151682268	AAAATTCAATTGCAG[G/T]GATGACTGCACAATT	4703
rs139770898	snp	A/C	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151528911	CTCAGGCACTTTCCA[A/C]AAATGCAACCTACAT	4703
rs139794371	snp	C/T	0.0221141	0.102801	intron-variant	NEB, RIF1	GRCh38.p7	2:151511392	TTTTACAATATACAA[C/T]TATATGTTTCCAGTA	4703
rs139798654	snp	C/T	0.00127501	0.0252167	NEB	2	allele_origin=T(germline)/C(germline)	2:151619579	ACTTCTTGGCCAAAA[C/T]GATACCAAGCATGTC	4703
rs139812390	snp	C/T	0.00597247	0.0543191	intron-variant	NEB, RIF1	GRCh38.p7	2:151495692	ACAACAAACAAAAAA[C/T]GAAAACTGGTAAAAC	4703
rs139834989	snp	C/T	0.00874735	0.0655527	intron-variant	NEB	GRCh38.p7	2:151574070	GCTCCGCCTCCTGGG[C/T]TTCACGCCATTCTCC	4703
rs139840492	snp	C/G	1.96574e-05	0.00313501	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151531875	TGTCCTTTGATTTTT[C/G]ATAGTTTTTCCTGTA	4703
rs139844745	snp	C/G	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151730270	GTGCTAATATGAAAA[C/G]TGGTAAATGCCAAGT	4703
rs139873336	snp	A/G	0.00398564	0.0444627	intron-variant	NEB	GRCh38.p7	2:151647981	TTGGGAAATACAGAC[A/G]GAATATTTAGGCATC	4703
rs139885226	snp	C/G	0.000233874	0.0108112	intron-variant	NEB	GRCh38.p7	2:151724836	TACTGAGTACCCCAG[C/G]CATCCATATCATTGC	4703
rs139886401	snp	C/T	0.00230887	0.0338985	intron-variant	NEB	GRCh38.p7	2:151682804	GTTACATTTCTTTGC[C/T]GTGTCATCCTCATTA	4703
rs139930220	snp	C/T	0.00257376	0.0357807	missense, intron-variant	NEB	GRCh38.p7	2:151592053	CTGATCTGCAGAGCA[C/T]TGATTTTGGATTGCA	4703
rs139957760	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151610704	AAAGGAAATTGTTAC[A/G]GTGGAAAAAGCATTT	4703
rs139960481	snp	A/C/G	0.0260105	0.111035	intron-variant	NEB	GRCh38.p7	2:151616475	GGGTGGATCACCTGA[A/C/G]GTCATGAGTTTGAGA	4703
rs139963368	snp	A/G	0.00476393	0.0485723	synonymous-codon	NEB	GRCh38.p7	2:151662303	AGGGAGCCATCCAAT[A/G]CCCTTCATGAAGTCA	4703
rs140039820	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151595944	AGAAAGCTTCTAGCA[C/G]AGGATGAGATGCAAT	4703
rs140046334	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151554587	AAGAAATGTTCCTAT[C/T]AATAATACATGGCTA	4703
rs140073759	in-del	-/AG			intron-variant	NEB, RIF1	GRCh38.p7	2:151500423	AGAGTTGTATATAAT[-/AG]ACACAAATAATTTGT	4703
rs140113688	snp	C/G	0.00676609	0.0577691	intron-variant	NEB	GRCh38.p7	2:151637743	GCACATGTAATGCAT[C/G]GTTTCCTGTAACAGG	4703
rs140124389	snp	A/G	0.000900105	0.0211953	intron-variant	NEB	GRCh38.p7	2:151538268	AGAAAAAACACATGA[A/G]TTACAAAAAAACTAC	4703
rs140130412	snp	A/G	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151614116	TATTTCAATATGATT[A/G]GTTTCTTCTGAAACT	4703
rs140134935	snp	A/G	0.00636936	0.0560724	intron-variant	NEB	GRCh38.p7	2:151689594	GGGAGTGTAAAGAAC[A/G]GATGAGGCTGTTTAA	4703
rs140146338	in-del	-/ATG			intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151499126	TAAATGATTATATTA[-/ATG]ATGTTTTACCAAAAT	4703
rs140169473	snp	C/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151569873	ATACAATTAAGACCT[C/G]TATTCATACTACCAT	4703
rs140171212	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151641149	CTGTATATTTATACA[C/T]ACAGAAAAAAAAGAA	4703
rs140171536	snp	C/T	0.420255	0.183066	intron-variant	NEB	GRCh38.p7	2:151557410	aagtccaggaccaga[C/T]ggattcacacctgga	4703
rs140186806	snp	C/T	0.0195673	0.0969576	NEB	2	allele_origin=T(germline)/C(germline)	2:151658007	AATATCTCTGGAAGC[C/T]TTGGCAGCTTTGATA	4703
rs140245557	snp	G/T	0.00438332	0.0466095	intron-variant	NEB	GRCh38.p7	2:151728140	AAAGTTTACTCCTTA[G/T]TACTTTGCAACATTG	4703
rs140268748	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151711164	AGCCTCAGAACCCAA[C/T]ACAAAATGCAGCACA	4703
rs140271590	snp	A/G	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151577503	CCATGGATCACTCTC[A/G]GCCATTCCATTTTTA	4703
rs140283704	snp	A/C	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151611756	AGCAACCTGAGCAAC[A/C]AATTTGAATGTGTAC	4703
rs140303554	snp	A/G	0.00279162	0.0372561	intron-variant	NEB	GRCh38.p7	2:151645001	CCACTGTAACACAAT[A/G]GGAAGTATTAATATT	4703
rs140306917	snp	A/G	0.00835141	0.0640778	intron-variant	NEB	GRCh38.p7	2:151734099	GGAACGTAGAGCAGC[A/G]TATCTTCTTTTTCAC	4703
rs140323673	snp	A/G	0.0018157	0.0300758	synonymous-codon	NEB	GRCh38.p7	2:151547441	TACATCACTGGTGAT[A/G]TCTCCCACATAGCGG	4703
rs140332440	in-del	-/A	0.040671	0.13668	intron-variant	NEB	GRCh38.p7	2:151658494	GTGGAATCTACAATT[-/A]AAAAAAAAAGGTCAG	4703
rs140342307	snp	A/G	0.00835141	0.0640778	intron-variant	NEB	GRCh38.p7	2:151616976	ATGTTAACATCAAAT[A/G]ATTATCAGAGCATAC	4703
rs140343145	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151542376	CCAAATCTACATATC[C/T]AGTGTCTTTCCTGAG	4703
rs140346451	snp	A/G/T	0.00358779	0.0422022	intron-variant	NEB	GRCh38.p7	2:151691356	CTAAGACGCCCATCC[A/G/T]GTCACTGTCTCACAC	4703
rs140378948	snp	C/T	0.00279162	0.0372561	intron-variant	NEB	GRCh38.p7	2:151564479	TTTTATAAGAGTTGA[C/T]TATTTTTGCGGTCCT	4703
rs140387522	snp	A/C	0.00716266	0.059414	intron-variant	NEB	GRCh38.p7	2:151667597	CTGGAGTGCAATCAC[A/C]GCTCACTGCAGCTTC	4703
rs140432671	snp	A/C	0.0154538	0.0865337	intron-variant	NEB	GRCh38.p7	2:151635339	CTTGATTTTTAGAGC[A/C]GTCATTTGTTCCTCA	4703
rs140439578	in-del	-/A	0.00755907	0.0610114	intron-variant	NEB	GRCh38.p7	2:151720597	CATTGTTCAAAGTCC[-/A]TAGCATTAGAATGGT	4703
rs140452327	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151678306	ACTTCAATAACCAAA[C/T]AATTAACAATTCACT	4703
rs140461027	snp	A/G	0.00676609	0.0577691	intron-variant	NEB, RIF1	GRCh38.p7	2:151521353	ACAAAGTAAAGGAAA[A/G]AGAAACGTAAACAAA	4703
rs140467309	snp	C/T	0.00478085	0.0486577	intron-variant	NEB	GRCh38.p7	2:151546637	GATCTTGGCTGACTG[C/T]AACCTCCGCCTCCCG	4703
rs140534629	in-del	-/C	0.0341408	0.126114	intron-variant	NEB	GRCh38.p7	2:151680272	GTAGGAACCTCTGGG[-/C]CCTAGCTCAGGAAAG	4703
rs140535618	snp	C/T	0.0170251	0.090679	intron-variant	NEB	GRCh38.p7	2:151631052	AAAAATGCGACCCCA[C/T]GCCTTCATAGATAAT	4703
rs140549936	snp	C/T	0.0298908	0.118541	intron-variant	NEB, RIF1	GRCh38.p7	2:151517842	AATCTTATGGGACCA[C/T]TGTCATACAGGTGGT	4703
rs140550265	snp	G/T	0.00170352	0.0291352	intron-variant	NEB	GRCh38.p7	2:151568578	GCTTTGGAAGTGATA[G/T]CTGCATCACTGTGAG	4703
rs140558263	snp	A/G	6.62515e-05	0.00575512	synonymous-codon	NEB	GRCh38.p7	2:151671098	TGTGAACTTGACGGT[A/G]TCTGGGTGCTGTCGA	4703
rs140596632	snp	A/G	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151561988	ATTGGGAGAGGAGGG[A/G]CTTTGGTCAGTTAGA	4703
rs140597189	snp	C/T	0.00438332	0.0466095	intron-variant	NEB	GRCh38.p7	2:151566812	TGCTATCATCTAATA[C/T]TGTCAAAACCTCAAC	4703
rs140607495	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151717181	TTCTGTTTTCAAAAG[A/G]TGATTTTCACATTTA	4703
rs140608564	snp	A/G	0.00716266	0.059414	intron-variant	NEB	GRCh38.p7	2:151668939	TCCACACTGAATTGC[A/G]CCCCCTACAATTCTC	4703
rs140631079	snp	C/G/T	0.0079613	0.0626594	intron-variant	NEB	GRCh38.p7	2:151708940	CCTGGTCCAAAACAC[C/G/T]GTCTTACACGTGGAT	4703
rs140642617	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151525590	GCATTATTGATAAGG[A/G]TAGAGCAGGCAGAGA	4703
rs140669305	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151672863	TACAAGTGAGTGTCA[C/T]GATAAATTCAAGATC	4703
rs140681231	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151690167	AGGTCTGAGAAGCAC[A/T]GCTGTTTTCCCCCGA	4703
rs140687709	snp	A/C	0.00398564	0.0444627	intron-variant	NEB, RIF1	GRCh38.p7	2:151520075	AAGGCTTCAGGCTAA[A/C]TTCAGAGATGTGATT	4703
rs140688592	snp	A/C	0.0184596	0.0942858	synonymous-codon	NEB	GRCh38.p7	2:151570566	CCGGACATCACAGCC[A/C]GCCTTCATTTCATCC	4703
rs140837131	snp	C/T	0.00358779	0.0422022	intron-variant	NEB	GRCh38.p7	2:151683771	TCACATGCCCATATT[C/T]ATAGCAGCATTATTC	4703
rs140838871	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151545063	ACACTCTAGGTGAGA[C/G]AATCAGATCTATTCA	4703
rs140856614	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151552152	GAGTTAATAAAGAAA[C/G]AGCAGCTTTGTGCCT	4703
rs140864353	in-del	-/AAC/AACAACA	0.09169	0.193768	intron-variant	NEB, RIF1	GRCh38.p7	2:151500143	TCCAAAAGACATATT[-/AAC/AACAACA]AACATTGAAAATTTA	4703
rs140890564	snp	C/G	0.00478085	0.0486577	intron-variant	NEB	GRCh38.p7	2:151547866	ATATAGAAAATGATT[C/G]AGATTAGGAAAAAAG	4703
rs140894724	snp	C/T	0.00318978	0.0398085	intron-variant	NEB	GRCh38.p7	2:151649947	TTTTCCCATTATATT[C/T]TGGTTAAATAATAAA	4703
rs140896726	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151695926	ATGTTCCCCTCCCTG[A/C]GTAGCACAATTGTCC	4703
rs140916608	snp	C/T	0.00398564	0.0444627	intron-variant	NEB, RIF1	GRCh38.p7	2:151501709	CAGCTGCCAGGCTGC[C/T]GGCAGGAGTGGCTTG	4703
rs140937844	snp	A/G	0.00398564	0.0444627	intron-variant	NEB	GRCh38.p7	2:151692523	AATAGATGTGGTAGA[A/G]GCTCATGCCTTATAT	4703
rs140954520	snp	G/T	0.00318978	0.0398085	intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151496862	TGTCTTTAGAAAATA[G/T]GATTAATATGTATTA	4703
rs140956188	snp	G/T	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151549881	ATTGATTTCAGGAGA[G/T]AATTAAATACATTCT	4703
rs140959933	snp	C/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151502350	AATACCACCTGTACC[C/T]CCCAAACTTATGGAA	4703
rs140962931	snp	C/G	0.00755907	0.0610114	intron-variant	NEB	GRCh38.p7	2:151611100	ATGAAGCAATATAAT[C/G]GTTGCTATTAGTAAT	4703
rs140966488	snp	A/C	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151651835	AACTTCAACATAAGC[A/C]ATCTGACAAAATTGC	4703
rs140967744	snp	A/G	0.000348325	0.0131925	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151503386	CGTTTGACTCTCTCA[A/G]TCTCTGGAGTCACAG	4703
rs140982447	snp	A/T	0.000350312	0.01323	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151526171	ACCTCAGACACCAGG[A/T]TGCTGACAGTCTTCG	4703
rs141004509	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151673502	TTTCTACTTAGACTA[C/G]AAATGTATTTCATAG	4703
rs141073469	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime	NEB	GRCh38.p7	2:151734433	TTCCTCAGCAGCAAA[A/G]CCTCTCCCAACTCTC	4703
rs141084270	snp	A/G	0.00159617	0.0282053	intron-variant	NEB, RIF1	GRCh38.p7	2:151518621	AGATGTAAACACTTA[A/G]GTTATGTGGCTTGTT	4703
rs141084946	snp	C/T	0.0189856	0.0955633	intron-variant	NEB, RIF1	GRCh38.p7	2:151519533	TGGTATGAAAACATT[C/T]TGGAAATAGTGACAG	4703
rs141088433	snp	A/G	0.0152123	0.0858763	intron-variant	NEB	GRCh38.p7	2:151626996	TCCTACAAATTGGGG[A/G]CTCACCTTGTTCATA	4703
rs141089924	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151627443	CCCTTCTGAAGGTTC[C/T]ACCTAATGCTAGACC	4703
rs141094882	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151655090	CTGCTCCACAAAGCA[C/T]ACAGTTGTGGCTGAA	4703
rs141120434	in-del	-/TC			intron-variant	NEB	GRCh38.p7	2:151690972	TCACTTCTCTGTCTG[-/TC]TCTCTCTCTCTCTCT	4703
rs141131711	snp	C/T	0.0111196	0.0737302	intron-variant	NEB	GRCh38.p7	2:151622394	AATGAAATCTTTATA[C/T]TATCACACTTAGTCA	4703
rs141134755	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151507234	TTGTTTTTGTTTAAG[C/T]ATCCCTTGCTTAGTA	4703
rs141150620	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151548550	TATGTAGAAAAGTCA[C/T]TGACAAAATTTCAAT	4703
rs141155976	snp	C/G	0.00288222	0.0378524	missense, intron-variant	NEB	GRCh38.p7	2:151650675	AGTCCACGTCACTAA[C/G]CAACTCCTGACACTT	4703
rs141178569	snp	A/C/G	0.000530296	0.0162753	intron-variant	NEB, RIF1	GRCh38.p7	2:151514292	TGCTGTATGAATTAC[A/C/G]TGCAGGCAGTCAGCT	4703
rs141186475	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151676214	AATAATAAATAATTT[A/C]TTCTAGGACCCAAAG	4703
rs141221298	snp	A/C/G	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151636810	AAACAAAAAAAAAAG[A/C/G]TACCCATAAAGCCCA	4703
rs141240053	snp	C/T	0.000368948	0.0135771	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151494166	AAGACAATACCGAGC[C/T]AATGTTTTCTTGATT	4703
rs141261492	in-del	-/AT	0.120326	0.21374	intron-variant	NEB, RIF1	GRCh38.p7	2:151487766	TTTATACATACACAC[-/AT]ATATATATATATGTA	4703
rs141292016	snp	C/T	0.00517822	0.0506191	intron-variant	NEB	GRCh38.p7	2:151631711	GAATCAATTTTAGGC[C/T]GAGGCAAATGGAACA	4703
rs141298223	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151709254	AATTGCCTCTTCCTG[C/G]GGGGAGAAGTCCTGC	4703
rs141330436	snp	C/T	0.00318978	0.0398085	intron-variant	NEB	GRCh38.p7	2:151566140	GTTATTTTCTGCTAT[C/T]GTCATAAGAAAAGGC	4703
rs141338915	snp	C/G	0.0267878	0.112589	NEB	2	allele_origin=G(germline)/C(germline)	2:151563606	TGGACATTTACTTAC[C/G]GCACTCCTCATCTTT	4703
rs141353276	snp	C/T	0.0154538	0.0865337	intron-variant	NEB	GRCh38.p7	2:151634886	CTAGCCTCACATGTA[C/T]CAACAATGTTTTTAT	4703
rs141355715	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151712235	GCAATTGGGCCTGAT[C/T]CCCAAAACTGAGATC	4703
rs141377412	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151632811	AGAGAAGGTGCCCAA[C/T]AAATAGACAGATGGT	4703
rs141430270	snp	C/T	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151683482	TCTGGGCATTTTAAG[C/T]AGAATGGAAAATCAA	4703
rs141442644	snp	A/G	0.0174175	0.0916809	intron-variant	NEB	GRCh38.p7	2:151698458	TGGGGGGATTAAAAA[A/G]AATTCTGGAATGAGA	4703
rs141449286	snp	A/G	6.62888e-05	0.00575674	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151485905	TCTGCATCAGCAGCC[A/G]TATAGTCATACATGG	4703
rs141468627	snp	A/T	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151679446	TAAGTCACTTCTGGA[A/T]CTCCACAAGAGAAGT	4703
rs141483727	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151589465	AAGATGGCGAAAACC[C/T]GCCTCTAATAAAAAT	4703
rs141501194	snp	C/G	0.0103295	0.0711199	intron-variant	NEB	GRCh38.p7	2:151609337	AGATCTCACATGATT[C/G]AGGGTTTTTAATATT	4703
rs141503992	snp	C/G	0.000145592	0.00853082	intron-variant, utr-variant-3-prime	NEB, RIF1	GRCh38.p7	2:151497754	CAGAAAAACAACCAT[C/G]AGTAACATTTCATTT	4703
rs141526973	snp	C/T	9.95818e-05	0.00705556	synonymous-codon	NEB	GRCh38.p7	2:151553407	ACTCACATCATCACG[C/T]AGATCATAAGCATGC	4703
rs141535165	snp	C/T	0.00676609	0.0577691	intron-variant	NEB	GRCh38.p7	2:151686209	ACATACCAGTACATA[C/T]AAAATGTTGTCAAAG	4703
rs141545609	snp	A/G	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151575426	TGCATCTCTTCATTC[A/G]TCTTTCACCTTCTTT	4703
rs141550837	snp	C/G	0.00358779	0.0422022	intron-variant	NEB	GRCh38.p7	2:151681774	TTGCTGCCTTATGAG[C/G]CTCAAGATCATCACT	4703
rs141586484	snp	C/T	5.0109e-05	0.0050052	intron-variant	NEB, RIF1	GRCh38.p7	2:151492511	TGATGCAGGAGAGAC[C/T]GTGAATGAGTGGTGC	4703
rs141600510	in-del	-/TGTATATATATATATATATATATATATATATATA			intron-variant	NEB	GRCh38.p7	2:151620346	ATATATGTATGTGTG[lengthTooLong]TATATATATATATTT	4703
rs141618371	snp	G/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151535293	TGACATTTTGGTGCC[G/T]TAGTAGAGGATACTA	4703
rs141633082	snp	C/T	0.0271762	0.113356	intron-variant	NEB	GRCh38.p7	2:151613432	CTGGCATCAGTGAAC[C/T]TGGATAGAAAAAATA	4703
rs141642565	snp	C/G	0.00318978	0.0398085	intron-variant	NEB	GRCh38.p7	2:151719633	CTCACGCCTGTAATC[C/G]CAGCACTTTGGGAGG	4703
rs141657883	in-del	-/ATTT	0.00755907	0.0610114	intron-variant	NEB	GRCh38.p7	2:151655011	ATTTTTTTTCAACAA[-/ATTT]TTTTCTATTGATTTC	4703
rs141674862	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151684454	TTTATTGAGAACTCA[C/T]CAGGGCCTGGCACCA	4703
rs141698756	snp	G/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151573533	AGAAAATACATCAGC[G/T]CCCTAAAATTATATT	4703
rs141703040	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151675648	TGGAAGGTAAATTCA[A/T]CCATGAAACCCTAGC	4703
rs141716857	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151534582	CCATCTTTGCATATG[A/G]TGCCATTAACAACAT	4703
rs141782215	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151521188	ACACATCCAGCACAA[C/T]AGACACAAAATAACA	4703
rs141800746	snp	C/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151666497	AAAGCCAACTTCAGT[C/G]TGAATCTAGGTAACA	4703
rs141807057	snp	G/T	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151670777	GTATCTGCTTATGAA[G/T]AGCACAGGCTCTCTA	4703
rs141830788	in-del	-/AAAC	0.11228	0.208646	intron-variant	NEB, RIF1	GRCh38.p7	2:151509359	CTGGGAAAAGAATAG[-/AAAC]AAACAATCGTCCTTT	4703
rs141888573	snp	C/T	0.103438	0.202533	intron-variant	NEB	GRCh38.p7	2:151559472	TTATAAATCATTCTA[C/T]TATAAAGACACATGC	4703
rs141890163	snp	C/T	0.00279162	0.0372561	intron-variant	NEB	GRCh38.p7	2:151659329	TGAGACAGAGTCTTG[C/T]GCTGTCACCCAGGCT	4703
rs141892461	snp	C/G/T	0.00279162	0.0372561	intron-variant	NEB	GRCh38.p7	2:151660731	CAGCCAGAGACCACA[C/G/T]GCCAACAAACAGCTG	4703
rs141910334	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151706764	GTTCCAATGAACCTA[C/T]CACTCCATAACCTTA	4703
rs141919540	snp	G/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151509629	TTTTTTTTTTGTTTG[G/T]TTGGTTTTTTGTTTT	4703
rs141925007	snp	A/G	0.0221141	0.102801	intron-variant	NEB, RIF1	GRCh38.p7	2:151511558	AATCTACATCCCCAG[A/G]TGCCTATAAAGCACA	4703
rs141925015	snp	C/T	0.00015477	0.0087955	synonymous-codon	NEB	GRCh38.p7	2:151562617	ACATCATACATCACT[C/T]AAGATCTCCTGGGCG	4703
rs141927119	snp	C/G	0.0228947	0.104514	intron-variant	NEB	GRCh38.p7	2:151561505	CTTGACTGAGACTGG[C/G]GTTGAGATTTTGGCC	4703
rs141930814	snp	C/T	0.021026	0.100354	NEB	2	allele_origin=T(germline)/C(germline)	2:151663744	CCCTTCTTGTATTCC[C/T]GGTCTGACTGCATCT	4703
rs141933669	snp	A/G	0.00438332	0.0466095	intron-variant	NEB	GRCh38.p7	2:151723837	CAATGTAAGGAGCCA[A/G]GAAGCACTTCACATA	4703
rs141948252	snp	A/G	0.0209421	0.100162	intron-variant	NEB, RIF1	GRCh38.p7	2:151510877	TTGTATTAACCCCCA[A/G]GTATGAGGTTTAAGA	4703
rs141955633	snp	C/T	0.0123036	0.0774623	intron-variant	NEB	GRCh38.p7	2:151646848	AGAAACAGGGTTTCG[C/T]TACGTTGTGCAGGCT	4703
rs141962711	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151560430	AGGCAGTGAGCACAT[A/G]GACTCTAATGACTGA	4703
rs141971613	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151608736	GGTGAAACCCCATCT[C/T]TACTAAAAATACAAA	4703
rs141974681	snp	C/T	0.00676609	0.0577691	intron-variant	NEB	GRCh38.p7	2:151662013	ACAAGACTCTTTTTC[C/T]AGGTAAAATAACCTC	4703
rs141976907	snp	G/T	0.001558	0.0278671	intron-variant	NEB	GRCh38.p7	2:151709640	CATCAAGATAAATGG[G/T]ATGATTTCCTCATAC	4703
rs142021061	snp	C/T	0.00119737	0.0244387	intron-variant	NEB, RIF1	GRCh38.p7	2:151516187	CCAAATTACATTCAG[C/T]ATAATTTGTGTTGGG	4703
rs142042367	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151513748	GCTACTACTAGGTAA[C/T]AAACATACAGGGTGA	4703
rs142074817	snp	A/C/G	0.0014411	0.026805	synonymous-codon	NEB	GRCh38.p7	2:151666141	CACATTCAAGGCATC[A/C/G]GGCAGGAGAGTGTAG	4703
rs142090788	snp	A/G	0.0138799	0.0821421	intron-variant	NEB	GRCh38.p7	2:151626385	CTCCCAAAAGTGTTG[A/G]GATTACAGGTGTGAG	4703
rs142095168	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151704815	ATGCAGAAATCACCC[A/G]TCTTCTGCGTCGCTC	4703
rs142173574	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151556852	ACTCAGAATCTCTGG[C/G]ACACATTTAAAGCAG	4703
rs142175579	in-del	-/C			intron-variant	NEB	GRCh38.p7	2:151718657	GCACCCAGGGTGCTG[-/C]CCTTTCCAGCATATC	4703
rs142198386	snp	C/T	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151695355	CTGGTTACAATACTA[C/T]ATATTACGATTATCT	4703
rs142204833	snp	A/G/T	0.00113791	0.0238266	intron-variant	NEB	GRCh38.p7	2:151723530	AGGAAGTAGGGTCAC[A/G/T]TTTACACAAAATACA	4703
rs142261429	snp	A/G	0.00358779	0.0422022	intron-variant	NEB	GRCh38.p7	2:151690171	CTGAGAAGCACTGCT[A/G]TTTTCCCCCGATCTT	4703
rs142265485	snp	A/C	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151721785	TTGTGAATCTGTGAG[A/C]TACAGAATCAAAAAG	4703
rs142281352	snp	C/T	0.00318978	0.0398085	intron-variant	NEB	GRCh38.p7	2:151616311	GATTTTACTGACTTG[C/T]AAATTTCAACAAAAA	4703
rs142291754	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151720118	TGTTGTTATGGAGAA[C/T]AATCTGATTTTTAAA	4703
rs142302879	snp	C/T	0.00438332	0.0466095	intron-variant	NEB	GRCh38.p7	2:151639486	AAAAAGAAAAGGTTA[C/T]GTGTTTTATACACAT	4703
rs142314464	in-del	-/AACA	0.0540128	0.155206	intron-variant	NEB, RIF1	GRCh38.p7	2:151512887	GTTTGCAATGTGCAC[-/AACA]AACAGTTGTTGGCTT	4703
rs142319849	snp	A/G	0.00398564	0.0444627	intron-variant	NEB	GRCh38.p7	2:151540103	TGCTGCTGAAGAATT[A/G]TAAGAAAGGGTCATA	4703
rs142323216	snp	A/G	0.00636936	0.0560724	intron-variant	NEB, RIF1	GRCh38.p7	2:151489236	TATCAATCCTAAAGT[A/G]TTAGGCTTTTGAGGA	4703
rs142325259	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151543834	GTGTATTATATTTCC[C/T]CTGTACTTAGGTATG	4703
rs142325512	in-del	-/GTG	0.11963	0.213316	intron-variant	NEB, RIF1	GRCh38.p7	2:151487047	TGTATGCATGAAATT[-/GTG]TGTGTGTGCGCATGT	4703
rs142326967	snp	C/T	0.000300531	0.0122546	missense, intron-variant	NEB	GRCh38.p7	2:151642597	CAATATCTCTGGAGG[C/T]CTTGGCTGCCTTGAT	4703
rs142346571	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151639153	GTGATTGAGAAATGC[A/C]AGAGTTGTTATTCAC	4703
rs142368531	snp	C/T	0.00358779	0.0422022	intron-variant	NEB	GRCh38.p7	2:151688478	TAGCTAAGGCATTAG[C/T]GCTGTTTTTAGAAAA	4703
rs142373645	snp	A/G	1.65836e-05	0.0028795	missense, intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151534253	TCTTAGCCAGCAGAT[A/G]TCTAGGCTCATCGAC	4703
rs142376886	snp	A/C	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151678245	AGGGCTTTACTAAAC[A/C]ATGAGGCCATGATTT	4703
rs142435476	snp	A/T	3.08866e-05	0.00392968	missense, intron-variant	NEB	GRCh38.p7	2:151630725	CCTACCTCACTGTAG[A/T]TGATTTTGTTCTGCC	4703
rs142454206	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151491099	GCAGTGGTACAATCA[C/T]GGCTCACTGCAGCTT	4703
rs142454476	snp	C/G	0.000728477	0.0190711	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151524519	GACACCCTTACCTCA[C/G]TGGCCTGTTTGGCTG	4703
rs142489742	snp	A/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151645681	AATTTTCAGATGTAT[A/T]CATTTCAGGAGATTA	4703
rs142510696	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151623220	CTTTCCCCCTTTCCT[C/T]TTTTAAGAGGTTTAT	4703
rs142519626	snp	C/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151519230	GAAACAACCCAAGTG[C/T]CTGTCAGCAGATGAA	4703
rs142540692	snp	A/G	0.000642011	0.0179051	missense	NEB	GRCh38.p7	2:151663564	TCACTTTGAATCTGC[A/G]TCATATTTTTGGCCA	4703
rs142556433	snp	C/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151527818	ATTTTTAAAGGCCTC[C/T]GGGTGAAATGATTCT	4703
rs142619248	snp	G/T	0.00478085	0.0486577	intron-variant	NEB	GRCh38.p7	2:151707480	TGCCTCACCTGCAAC[G/T]GTGCATGGAGCACAC	4703
rs142620932	snp	A/T	0.0119091	0.0762411	intron-variant	NEB, RIF1	GRCh38.p7	2:151512985	CTTCCTATTTTGTTC[A/T]TAGTTTTATACCAAA	4703
rs142627072	snp	C/T	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151621279	TATACATTAAATGAA[C/T]ACCTCTTAATGTGTT	4703
rs142634769	snp	A/T	0.0115144	0.0749975	intron-variant	NEB	GRCh38.p7	2:151705545	ACTGAAAATAGAACT[A/T]CCATTCAATCCAGCA	4703
rs142661296	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151697704	ACTCCCACGCTGATT[A/T]TAACACTTACATTTT	4703
rs142705808	snp	A/G	0.0448719	0.142907	intron-variant	NEB	GRCh38.p7	2:151704604	AAGCGCAATATTCGG[A/G]AGGGAGTGACCCGAT	4703
rs142728108	snp	A/G	0.00716266	0.059414	intron-variant	NEB	GRCh38.p7	2:151671325	GGGAAATGAATAGCA[A/G]CTCTTCAGCATGCTC	4703
rs142767014	snp	C/T	0.00199481	0.0315187	intron-variant	NEB, RIF1	GRCh38.p7	2:151516871	ATGGGGAAAATTACC[C/T]AGGTAGATGAGGTTG	4703
rs142773625	snp	C/T	0.00676609	0.0577691	intron-variant	NEB	GRCh38.p7	2:151714751	TATTTTTTTATACTT[C/T]AAGTTCTAGGGTAGA	4703
rs142777534	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151669891	CACGAGCCATACAGA[A/C]GCTGGAAGTAGGGTT	4703
rs142779425	snp	C/T	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151624828	AACAATTGAGCAAGA[C/T]GCTATTTATGCAGCA	4703
rs142792228	snp	C/T	0.00557542	0.0525036	intron-variant	NEB, RIF1	GRCh38.p7	2:151526768	GCTTGACTGCTGGCG[C/T]CCCTCACAGGACAGG	4703
rs142813503	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151551306	GATGGGAAATAACAT[C/G]AAAAGTTGAGACCAA	4703
rs142820583	snp	C/T	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151653437	TCTATGAACTTTAGA[C/T]TGGATTTTCAGAAAG	4703
rs142872250	snp	C/T	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151717294	TCTTTGGGGATCATA[C/T]GTAAAAATACTCCTA	4703
rs142873623	snp	C/T	0.00398564	0.0444627	intron-variant	NEB, RIF1	GRCh38.p7	2:151530427	ATCGTTGGGGAAGGA[C/T]CCTAGGTTTTAATGT	4703
rs142880846	snp	C/T	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151628568	ATTTTCAGCTGGGCA[C/T]AGTGGCTTATGCCTG	4703
rs142883671	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151635402	TTTTGCTCTGGGAGA[C/T]GTGCTAAATGGCTAG	4703
rs142886286	snp	A/C	0.0189856	0.0955633	intron-variant	NEB, RIF1	GRCh38.p7	2:151502293	CTTGGGTGATGGGTG[A/C]ACCAAAATCTCACAA	4703
rs142927650	in-del	-/T	0.0341408	0.126114	intron-variant	NEB, RIF1	GRCh38.p7	2:151490634	CATGGTTTTAAGTAC[-/T]TTCCCATGGGTCAAA	4703
rs142952391	snp	A/C	2.19339e-05	0.00331157	missense	NEB	GRCh38.p7	2:151565587	GATAGTTTTCAAGGG[A/C]ATTTTTCTTATATTT	4703
rs142954326	snp	C/T	0.00517822	0.0506191	intron-variant	NEB	GRCh38.p7	2:151667999	TCTTATAAAACATGT[C/T]GTAATAGATCCCTTT	4703
rs143001081	snp	A/T	0.00557542	0.0525036	intron-variant	NEB	GRCh38.p7	2:151711774	CCCACAGTGCTAAGC[A/T]AATATAGGGTATAAA	4703
rs143013662	snp	C/T	0.00478085	0.0486577	intron-variant	NEB	GRCh38.p7	2:151685044	AAAGACAGAGATCTT[C/T]CATAAACAATAAATA	4703
rs143014154	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151617703	ATTTAAAATAATTTA[C/T]AGGAAAGAGTTATAG	4703
rs143057229	snp	A/G	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151651882	CCATAGATTTTGTAT[A/G]GGGCACAAATAAGCT	4703
rs143069456	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151730233	AGTCCCTTTCAATAG[C/T]GTGATTGTCCTAAAC	4703
rs143123053	snp	A/G	0.00297761	0.03847	missense	NEB	GRCh38.p7	2:151687453	GTCTTCAAGGAGTGC[A/G]GCATCTTTGGATCGT	4703
rs143167672	snp	A/C	0.00874735	0.0655527	intron-variant	NEB	GRCh38.p7	2:151632137	TATAAAATCATATTG[A/C]CATATTTTTCTCACT	4703
rs143183246	snp	C/T	0.00199481	0.0315187	intron-variant	NEB, RIF1	GRCh38.p7	2:151493208	AAATTTTTATGGTGT[C/T]AAAACGTTACTTTCC	4703
rs143183687	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151505732	TCATTCTGATACTGG[A/G]TAAGAGGAGAACAAT	4703
rs143202961	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151541732	TTTTCTTTTTTCCCT[C/T]GTGTCAAAACAAGAG	4703
rs143208740	snp	A/G	0.00478085	0.0486577	intron-variant	NEB	GRCh38.p7	2:151643707	TGACTAGATGCGCTT[A/G]GGCATTAGTCCAGGG	4703
rs143226849	snp	G/T	0.0130921	0.0798413	intron-variant	NEB	GRCh38.p7	2:151655668	AAAAATAAGAGATGG[G/T]CAGAAGAAGATGGTG	4703
rs143237026	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	NEB	GRCh38.p7	2:151734725	TGAGGCCCCATTCAA[C/T]GTCATATTCATGCAA	4703
rs143238266	snp	C/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151733012	AAATGATGACTCTTT[C/G]TGAAGTTATAATAGA	4703
rs143265967	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151529658	GCCTCAGCCTCCTGA[A/G]TACCTGGGACCACAG	4703
rs143272241	snp	A/G	0.00358779	0.0422022	intron-variant	NEB	GRCh38.p7	2:151665602	TGTTTCTTTGGCTAT[A/G]TGATTTACTTACAAT	4703
rs143300394	snp	C/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151510343	CAGGAAAGGCCTAGC[C/T]GAAACTTTTGGTGGG	4703
rs143308808	snp	C/G	0.0154538	0.0865337	intron-variant	NEB	GRCh38.p7	2:151617946	GCTCCTGTAATCCCA[C/G]CTACTTGGGAGGCTG	4703
rs143310245	snp	C/T	0.0119091	0.0762411	intron-variant	NEB	GRCh38.p7	2:151575319	ACCCCCCGAGGTCCA[C/T]GTTTTAAAATTAATT	4703
rs143330412	snp	A/C	0.00557542	0.0525036	intron-variant	NEB	GRCh38.p7	2:151623626	TTATTAAGATGTGTC[A/C]GTTTATAGTCTTTTC	4703
rs143342172	snp	A/G	0.0410537	0.137264	intron-variant	NEB	GRCh38.p7	2:151613734	ATTCTCATGAGATCC[A/G]GGTGCTTAAAAGTGT	4703
rs143352368	snp	C/T	0.0023933	0.0345097	intron-variant	NEB, RIF1	GRCh38.p7	2:151515710	AGAATTTTAAATTTA[C/T]AGGAAAGTCACAAGA	4703
rs143433144	snp	C/G	0.0456336	0.143994	intron-variant	NEB	GRCh38.p7	2:151620109	GGCGTATGTTTACAT[C/G]GATCATTAAAATTTT	4703
rs143437615	snp	C/T	0.0162398	0.0886349	intron-variant	NEB	GRCh38.p7	2:151654832	TCATACCAAGTCTGT[C/T]TGATGCAATTTTTAC	4703
rs143456239	snp	A/G	0.00105444	0.022937	synonymous-codon	NEB	GRCh38.p7	2:151552762	TGTTTTCAACATGTG[A/G]GCTTTATACTTGATC	4703
rs143470269	snp	C/T	0.021333	0.101051	intron-variant	NEB, RIF1	GRCh38.p7	2:151512328	CATGAGCCACCATGC[C/T]GGGCTTCTCTCTTTT	4703
rs143473183	snp	A/T	0.000778062	0.0197085	missense, intron-variant	NEB	GRCh38.p7	2:151633887	CGTGCATGGACCACA[A/T]CATCTTGGGGTCATC	4703
rs143478654	snp	C/G	0.0178098	0.0926698	intron-variant	NEB	GRCh38.p7	2:151710784	TGCTGAGTTTGGGGA[C/G]TTCATTCATTCGGAA	4703
rs143504634	snp	C/T	0.00636936	0.0560724	intron-variant	NEB	GRCh38.p7	2:151718916	GAACTATTCATAGAT[C/T]CCCAGATACATGAAG	4703
rs143508594	snp	A/C	0.00755907	0.0610114	intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151507237	TTTTTGTTTAAGTAT[A/C]CCTTGCTTAGTAGAT	4703
rs143524804	snp	A/G	0.00279162	0.0372561	intron-variant	NEB	GRCh38.p7	2:151663088	TCTAAAGGCTGCCTC[A/G]GTCATCACCTTCTCA	4703
rs143524931	snp	A/C	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151616695	TGAAACTATGTCTCA[A/C]ACGTAACAAAACAAA	4703
rs143541168	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151649468	ATCCTCCTAATAACA[C/G]ACGGTTATTATATAT	4703
rs143582290	snp	A/G	1.67346e-05	0.00289258	missense	NEB	GRCh38.p7	2:151567385	TTCTGAATCTGGCCT[A/G]CATGCTCAAACCAAA	4703
rs143587644	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151669915	TAGGGTTGGTGGCAT[C/T]TGAGAGCAGACTGGC	4703
rs143602832	snp	C/T	0.00081346	0.0201511	missense, nc-transcript-variant, intron-variant	NEB, RIF1	GRCh38.p7	2:151506988	ATTTTTCCTTTACTG[C/T]TTTTAAGGTCACACT	4703
rs143607363	snp	C/T	0.00517822	0.0506191	intron-variant	NEB	GRCh38.p7	2:151713934	CATCTGAACTGGGAG[C/T]TGTAAGAAAAGGGTG	4703
rs143622692	snp	C/T	0.00159617	0.0282053	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151498748	GATATTTGGGTTTTA[C/T]AAACATTGTGTATAT	4703
rs143625642	snp	A/G	0.210301	0.246828	intron-variant	NEB	GRCh38.p7	2:151605726	AAATCAGAGAAGAAC[A/G]CAGAGAAAGGAACAA	4703
rs143644938	snp	C/G	0.000399281	0.0141238	splice-donor-variant, intron-variant	NEB	GRCh38.p7	2:151636226	GGAATTGACAACTCA[C/G]GTCACTGATGATGTC	4703
rs143652962	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151714146	AATCCTCCAACTCTC[A/C]CAAAGCACAGGCTCA	4703
rs143661332	snp	C/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151712421	TCTGGTTTTCAAGAA[C/G]ATATTAAAACAAGAT	4703
rs143684640	snp	A/G	0.000399281	0.0141238	synonymous-codon	NEB	GRCh38.p7	2:151570584	CTTCATTTCATCCCA[A/G]CCCTCACGGTAAAGT	4703
rs143690964	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151628322	AAATCCAGCTCTGCT[A/G]GGGCACTTGACTCCC	4703
rs143691486	in-del	-/GAC	0.021333	0.101051	intron-variant	NEB	GRCh38.p7	2:151719936	TCATTTTAGGCATAG[-/GAC]AACAGGATTTTTCAT	4703
rs143695780	snp	G/T	0.00557542	0.0525036	intron-variant	NEB	GRCh38.p7	2:151706723	CATTGTACTCAGAGG[G/T]ACTCATGCCTTTCTG	4703
rs143707816	snp	C/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151487968	ATATGATATTTGATT[C/G]AATTTGATACTTTGT	4703
rs143709169	snp	A/G/T	0.00159649	0.0282165	intron-variant	NEB, RIF1	GRCh38.p7	2:151486782	TGTATGGTTTTATTT[A/G/T]TATGAAATGTCTTAG	4703
rs143720079	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151571862	TAATTAGTGACAGTT[C/T]TGTAGCTTTTGCATG	4703
rs143761216	snp	A/G	0.00517822	0.0506191	intron-variant	NEB	GRCh38.p7	2:151567858	TTAAAAAAGCCAAGG[A/G]GGGTGGTGGGCGGGT	4703
rs143782058	snp	C/T	0.0178098	0.0926698	intron-variant	NEB	GRCh38.p7	2:151716297	GCGCCCGCCACCACG[C/T]CTGGCTAATTTTTTG	4703
rs143799133	in-del	-/A	0.0926964	0.194308	intron-variant	NEB, RIF1	GRCh38.p7	2:151520742	GTGGTGCACCCCTGT[-/A]AGTCTCAGCTACTCA	4703
rs143806212	in-del	-/A			intron-variant	NEB	GRCh38.p7	2:151574503	TAAGATTTTATTTTT[-/A]AAAAATAAGAATGGG	4703
rs143815307	in-del	-/ACA	0.00279162	0.0372561	intron-variant	NEB	GRCh38.p7	2:151706562	GCTTCTGTCAAAATC[-/ACA]ACACGTCTGCAATGT	4703
rs143823012	snp	C/T	0.00279162	0.0372561	intron-variant	NEB	GRCh38.p7	2:151638056	AAAATCTCCACAGGC[C/T]TATACCCACAGGCTC	4703
rs143891523	snp	C/G	0.00716266	0.059414	intron-variant	NEB	GRCh38.p7	2:151689683	GGCAGAGTCCATTGC[C/G]TACCTAAGCCAATAA	4703
rs143898397	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151574077	CTCCTGGGTTTCACG[C/T]CATTCTCCTGCCTCA	4703
rs143913273	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151614703	ATCATGAAGGAGAAA[A/G]GTGAGTATCATCAAC	4703
rs143932500	snp	A/G	0.000133837	0.00817929	intron-variant	NEB, RIF1	GRCh38.p7	2:151485962	TGGAAAAGGGGAAAT[A/G]TTATATGTTGGATTT	4703
rs143933602	snp	A/G	0.00219531	0.0330581	missense, intron-variant	NEB	GRCh38.p7	2:151636258	CTGGAGGCCTTGGCC[A/G]CCACGATGGGGATGG	4703
rs143936529	snp	A/G	0.00358779	0.0422022	intron-variant	NEB	GRCh38.p7	2:151641209	AATTTGTTATGATTC[A/G]TGTGTGAGAATATAA	4703
rs143937030	snp	C/T	0.00597247	0.0543191	upstream-variant-2KB	NEB	GRCh38.p7	2:151736196	ACATCTAGGTTGTTT[C/T]GAGGTTTTTGCTATT	4703
rs143944381	in-del	-/TTATCC	0.178465	0.239547	intron-variant	NEB	GRCh38.p7	2:151675770	CCTAGAGAGAAAGTA[-/TTATCC]GTAGTTAGAATAAGT	4703
rs143956956	snp	C/T	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151680959	TGCAAAAACACTAGA[C/T]TCTTGATTGGCTTGA	4703
rs143962561	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151549321	TCCAATAAATGGCTT[A/G]GGATAATTCAGGGTG	4703
rs143983527	in-del	-/TC			intron-variant	NEB	GRCh38.p7	2:151706338	TCATCACATATTCAA[-/TC]TCTCTCTCTCTCTCT	4703
rs143994653	snp	C/T	0.00159617	0.0282053	utr-variant-3-prime, intron-variant	NEB, RIF1	GRCh38.p7	2:151485661	GACACAGAAAAACCA[C/T]AGGCAGCTTGAGAAC	4703
rs144003002	in-del	-/A	0.0876345	0.190099	intron-variant	NEB	GRCh38.p7	2:151647061	TCCTTATGTCTCTTC[-/A]ACAGAAGACAAGGGG	4703
rs144004313	snp	C/T	0.0126979	0.078662	intron-variant	NEB	GRCh38.p7	2:151619319	ACCTCCAATGGGAAA[C/T]TCCTTTCAGACATTT	4703
rs144012829	snp	A/G	4.986e-05	0.00499274	intron-variant	NEB	GRCh38.p7	2:151694288	CAACTTTGTGGCCAC[A/G]TCTGAAAATAGGGGT	4703
rs144025991	snp	A/G	0.0111196	0.0737302	intron-variant	NEB	GRCh38.p7	2:151625900	CACGTGTGTGTGTTT[A/G]GTAACCAGGTCACTC	4703
rs144066670	snp	C/T	0.0119091	0.0762411	intron-variant	NEB	GRCh38.p7	2:151667524	TGATACAATCTTATA[C/T]ATCACATATAGATTT	4703
rs144077905	snp	C/G	0.0141221	0.082835	intron-variant	NEB	GRCh38.p7	2:151552815	CCATGTTGGACCATT[C/G]CTTATGCTTGAAACT	4703
rs144085789	snp	G/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151695847	GTGTGCAGGACACTT[G/T]GCAGCTATTATCACA	4703
rs144125469	snp	A/C	0.00438332	0.0466095	intron-variant	NEB	GRCh38.p7	2:151657110	TTTTCTGCCTGTCTC[A/C]TTTTGGGGTTGCGTG	4703
rs144168709	snp	C/T	0.000234761	0.0108317	missense	NEB	GRCh38.p7	2:151551817	ACTTTGCCTCTGACA[C/T]TGTGCACATAGTCAT	4703
rs144180333	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151711347	GCAATTCTCCCTCCA[C/T]GGCTCATAAAAATGT	4703
rs144180493	snp	A/C	0.00658094	0.0569839	missense	NEB	GRCh38.p7	2:151663756	TCCCGGTCTGACTGC[A/C]TCTTGGCCACTTGCA	4703
rs144221335	in-del	-/AA			intron-variant	NEB	GRCh38.p7	2:151589638	AGACTCTCCGTCTCA[-/AA]AAAAAAAAAAAAAAA	4703
rs144222420	snp	A/G	0.0209421	0.100162	intron-variant	NEB, RIF1	GRCh38.p7	2:151520571	CTAGGTAAAATATCT[A/G]AAGAGGATGATAGCC	4703
rs144225000	snp	A/G	0.0460142	0.144533	intron-variant	NEB	GRCh38.p7	2:151561882	ACACCTCCCAGATAA[A/G]CTTTTATTATAAATG	4703
rs144230150	snp	A/G	0.00438332	0.0466095	intron-variant	NEB	GRCh38.p7	2:151656931	TTACTGATGAGAAAA[A/G]TTTCAATTATGAGAC	4703
rs144253891	snp	C/T	0.00279162	0.0372561	intron-variant	NEB	GRCh38.p7	2:151672938	GAACTTTATTTTAAA[C/T]AAACTGAATTTTCAC	4703
rs144289060	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151615215	AAGTTTTGATAATAC[A/G]GTGTGTGTCCTTAAC	4703
rs144303545	snp	C/T	0.00076164	0.0194997	intron-variant	NEB, RIF1	GRCh38.p7	2:151518309	AAAAATCGGTCTTGA[C/T]CCACTTACTATACTC	4703
rs144312053	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151506509	TAACACAGGATGAGA[A/G]GAGCCAGGAAATGTT	4703
rs144336912	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151729185	GAAGCCCTGGAGACA[C/T]CATCCCTGGTGGCAG	4703
rs144344134	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151565231	AACATAATCAGTCCA[C/T]GTTTAAAGATTAAAA	4703
rs144373355	snp	C/T	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151536826	TAATCCCACTTTATA[C/T]TGGCTGTCATATCAG	4703
rs144376972	snp	A/G/T	0.00186971	0.0305193	missense, synonymous-codon	NEB	GRCh38.p7	2:151677703	TTTAACTTTTTCGAC[A/G/T]TCGAGACTGCCAATA	4703
rs144392345	snp	A/G	0.00438332	0.0466095	intron-variant	NEB	GRCh38.p7	2:151610299	TTGTAATGTAATCAT[A/G]TATCTTCATTGGTGA	4703
rs144400536	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151715422	CTATATCCCCACCCC[C/G]CAAATTCATATGTTG	4703
rs144423548	snp	A/C	0.0221141	0.102801	intron-variant	NEB, RIF1	GRCh38.p7	2:151521385	GCTACAATGGCTCTT[A/C]TCTGAAAAAGTTTCA	4703
rs144454775	snp	C/T	0.0115144	0.0749975	intron-variant	NEB	GRCh38.p7	2:151637526	AACATCAGAGGGGAG[C/T]GCCCATGGCAGCGTC	4703
rs144460445	snp	A/G	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151711587	AGCCAACTGGTTTTC[A/G]TAGCTATAAATTTTA	4703
rs144475008	snp	A/C	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151488507	AAAAAATTAGCCTAG[A/C]ATGGCATATACACCT	4703
rs144481986	snp	A/C	0.00318978	0.0398085	intron-variant	NEB	GRCh38.p7	2:151725104	ATTTTAGCTGGAAAA[A/C]TGTGATCTTCAAAGA	4703
rs144496499	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151640845	ACATATGAAATATAT[A/G]TCTTATATAAAATAT	4703
rs144503367	snp	A/G/T	2.61236e-05	0.00361402	intron-variant	NEB, RIF1	GRCh38.p7	2:151531775	TTGAGAAGGTATTCA[A/G/T]TGTTTCTTGCACTTA	4703
rs144539316	snp	C/T	0.000559416	0.0167151	missense	NEB	GRCh38.p7	2:151560687	CTCTATCCCAGGCCT[C/T]CTTGTACAGGTTCTG	4703
rs144545240	snp	A/C/G	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151528940	ATTTCAGAATTAAAC[A/C/G]TCCCATTTCTCAGCC	4703
rs144545947	snp	A/G	0.00517822	0.0506191	intron-variant	NEB	GRCh38.p7	2:151663159	GGTAGAATGAAACCC[A/G]GTTGGGAGGGAGGGG	4703
rs144547460	snp	C/T	0.0154538	0.0865337	intron-variant	NEB	GRCh38.p7	2:151634716	ACCTGTAGTAGCAAC[C/T]GAGGAGAATTTATTA	4703
rs144549350	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151682373	ATAAAATTGTTAAAA[A/C]TATTTCTATAATGAA	4703
rs144569150	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151586541	AATAGGGAATCAATA[C/T]CTGAAACATTAAGCC	4703
rs144586009	in-del	-/G	0.117537	0.212022	intron-variant	NEB, RIF1	GRCh38.p7	2:151489381	GGCATGTATATATGT[-/G]GGCACATTGCATACA	4703
rs144595998	snp	A/G	0.000759975	0.0194784	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151642828	ATCTGGCATAATGTG[A/G]ACAGTGGTTTTATCT	4703
rs144601709	snp	G/T	0.00279162	0.0372561	intron-variant	NEB	GRCh38.p7	2:151723150	TGACCCCAGATTCAG[G/T]TTTGCCACCTATAAG	4703
rs144632631	snp	G/T	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151540611	CATTTATAGTAATGA[G/T]CTCTCTGATCAGAGG	4703
rs144634228	snp	C/T	0	0	missense, intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151499354	CTGGAGTGATGGGGA[C/T]TGGAATCCCTTTTCC	4703
rs144637168	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151654693	AATTTCCCATTTAGT[C/T]CTCATGGCAATCCAA	4703
rs144673752	snp	A/G	0.000132923	0.00815132	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151619715	GTGTACTGCTCGGGC[A/G]CCAATGTGGTGACCC	4703
rs144676860	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151695061	TTATAGAATTATTGA[A/T]GAAATTGAGAACCCC	4703
rs144680661	snp	C/G	3.81098e-05	0.00436502	intron-variant	NEB	GRCh38.p7	2:151727917	ATTGTCTGAAAATTT[C/G]ATATGCAGTTCAACA	4703
rs144709880	snp	C/T	0.00664	0.0572356	missense, intron-variant, utr-variant-3-prime	NEB, RIF1	GRCh38.p7	2:151497662	GTGTTTGACTCTTTC[C/T]ATCTCGGGAGTGACA	4703
rs144722317	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151650069	AATTTTATGTGGTGA[C/T]GTATGAGGCAATGCT	4703
rs144735118	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151550664	TATTTTTGAGACAGG[G/T]TCTCACTGTGTCACC	4703
rs144760391	snp	A/G	0.0154538	0.0865337	intron-variant	NEB	GRCh38.p7	2:151647856	ATTTTCTTTTCTTAT[A/G]AAGGATATTAGTGAT	4703
rs144769173	in-del	-/AT	0.0205511	0.0992634	intron-variant	NEB	GRCh38.p7	2:151641314	ATAGTCTTTGCACAC[-/AT]GACTGTTTTTTTTGT	4703
rs144791747	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151504216	GGCGTGGGGAGCAAC[A/G]TACCCAGATTTTAAT	4703
rs144800068	snp	C/T	0.00835141	0.0640778	intron-variant	NEB	GRCh38.p7	2:151611628	CTCATTGGATAAAAA[C/T]AGATTGATAAAATTT	4703
rs144823501	snp	C/G	0.00597247	0.0543191	intron-variant	NEB, RIF1	GRCh38.p7	2:151529784	TCCCGCCCACCTCAG[C/G]CTTTCAAAGTGCTGG	4703
rs144836165	snp	A/G	0.00225236	0.0334829	intron-variant	NEB	GRCh38.p7	2:151610640	TAGGGAAGGGATAAT[A/G]GACGACAGAAAATAA	4703
rs144841789	snp	C/T	0.0154538	0.0865337	intron-variant	NEB	GRCh38.p7	2:151646728	AATCATGGCTCACTG[C/T]AACCTCTGCCTCCTG	4703
rs144867082	snp	A/G	0.0123036	0.0774623	intron-variant	NEB	GRCh38.p7	2:151658332	ACTGGTCTCTATTAG[A/G]TTGTAAATATACTTT	4703
rs144873265	in-del	-/TGTC			intron-variant	NEB	GRCh38.p7	2:151625323	ATGAAGATATTTTTG[-/TGTC]TGTCTGTCTATCTGT	4703
rs144875348	in-del	-/AGTGAGAT	0.0352966	0.128072	intron-variant	NEB, RIF1	GRCh38.p7	2:151519137	ACTAATGGAAATCAA[-/AGTGAGAT]AGCCCATCGTCAAAC	4703
rs144948242	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151509430	TAAGCAAAAGCTACC[C/T]CAACTGGTTTGCAGA	4703
rs144954552	snp	C/T	0.00835141	0.0640778	intron-variant	NEB	GRCh38.p7	2:151617204	TACTTTGTGGACCCA[C/T]CACAAAGCTCAAAAT	4703
rs144979692	snp	C/T	0.00358779	0.0422022	intron-variant	NEB	GRCh38.p7	2:151706775	CCTACCACTCCATAA[C/T]CTTAATGTATTTGCA	4703
rs144993309	snp	G/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151517524	TTATAGTCATGAATT[G/T]CTTAACAACTGGGAT	4703
rs145009109	snp	A/T	0.00874735	0.0655527	intron-variant	NEB	GRCh38.p7	2:151705201	TGAACTGGTACTAAG[A/T]GTTACTACTAACTCT	4703
rs145031304	snp	A/C	0.000399281	0.0141238	missense	NEB	GRCh38.p7	2:151562199	TCAACCAATTCAGGT[A/C]ATCTTTATACACATT	4703
rs145034441	snp	A/G	0.0154538	0.0865337	intron-variant	NEB	GRCh38.p7	2:151634948	TAAGCCAGTTATCCA[A/G]AATACATGCTTCTAG	4703
rs145052299	snp	A/G	0.0152103	0.0858708	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151627005	TTGGGGGCTCACCTT[A/G]TTCATATTGAGAGCA	4703
rs145062151	snp	C/G/T	0.000102586	0.00716131	intron-variant	NEB	GRCh38.p7	2:151540650	GAAGGTTTTAACAAA[C/G/T]TATTTTTCTTTTTAC	4703
rs145079286	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151631773	GAATATTTATGACAT[A/G]TAGAAATGTCATTAA	4703
rs145102225	snp	G/T	0.00835141	0.0640778	intron-variant	NEB	GRCh38.p7	2:151611353	GATCCATAACATATA[G/T]AAAATGCCCAAGTCA	4703
rs145112154	snp	C/T	0.000732747	0.0191269	intron-variant	NEB	GRCh38.p7	2:151687402	TGAAAACAAGACAGA[C/T]TCACAAAGACACTCA	4703
rs145127681	snp	A/G	0.0610702	0.163724	NEB	2	allele_origin=G(germline)/A(germline)	2:151561114	TATATTTTACCTGTA[A/G]ACAAGCAACAATAGG	4703
rs145168437	snp	G/T	0.0193772	0.0965046	intron-variant	NEB	GRCh38.p7	2:151630122	TTAAAAGACAAATAA[G/T]AAAAATTAAAATATA	4703
rs145180847	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151708753	TATCTGAAGATGAGC[C/T]CTTGTCTGTCCTCCA	4703
rs145228169	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151490716	AGCTTACGTACATGA[C/T]CAAAGGTCATGGAAC	4703
rs145230109	snp	A/C	0.00358779	0.0422022	intron-variant	NEB	GRCh38.p7	2:151684506	TTACATCCTCCAAAC[A/C]ATGTTTTTGATTTAT	4703
rs145232072	snp	C/T	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151734193	CAAGCAATAAATTGG[C/T]TAGCAAAGGACTTGA	4703
rs145252235	snp	C/T	0.0245199	0.107976	NEB	2	allele_origin=T(germline)/C(germline)	2:151563847	CACCAGATCAGCATG[C/T]TTGGCTCCAACAATG	4703
rs145255277	snp	A/G	0.00557542	0.0525036	intron-variant	NEB	GRCh38.p7	2:151642474	TAAACTGTTAGCAAC[A/G]GCTTTAACCTCATGG	4703
rs145261555	snp	G/T	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151720655	TGATAGATGAAGGGA[G/T]ATAGGAGATTAACTG	4703
rs145274409	snp	A/G	0.00438332	0.0466095	intron-variant	NEB	GRCh38.p7	2:151728480	GATTTTCATTCCCTT[A/G]GCTTAGTCAGTTAAT	4703
rs145298277	snp	A/G	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151664970	AGAGGTTAAATGGAT[A/G]TTAGAAAATGGATGA	4703
rs145305378	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151617066	TACTTGCTAGCTGCT[A/G]AATAAAATAATGACT	4703
rs145307633	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151542973	TTACTGGAACTCATT[A/G]TGGCTGCTTTCACAG	4703
rs145339817	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151731560	GAGATCTCAGTTCAA[C/T]ACTTTCTGGCAGGCA	4703
rs145350746	snp	A/T	0.00358779	0.0422022	intron-variant	NEB	GRCh38.p7	2:151688235	GTCTTTTAAAATTTA[A/T]AACATTTTCTCTTTT	4703
rs145364438	snp	C/T	0.220843	0.248294	intron-variant	NEB	GRCh38.p7	2:151605418	TAGGGAGAGGTCATA[C/T]GTGTGTGGTTTTGGA	4703
rs145367730	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151574854	CTCCCACCTGAGCCT[C/T]CCAAGTAACTTGGGC	4703
rs145376497	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151709234	TATCTTCATATAAGG[C/T]CACCAATTGCCTCTT	4703
rs145381118	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151579109	AAAAAAAAAAAAAAG[A/T]AAGAAACTGGAAACA	4703
rs145394900	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151612730	ATGGAAACTGTACTG[A/G]GTGAGAATACAGTTG	4703
rs145437130	snp	C/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151696353	TGGCCACCCAGACAT[C/G]AATGACAGAGCTAAC	4703
rs145442121	snp	A/G	0.00279162	0.0372561	intron-variant	NEB	GRCh38.p7	2:151539093	CTATTGTAAAGATTA[A/G]AGTTATCAGAATTGC	4703
rs145474632	snp	A/G	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151634499	ATAAAAAAATAAGCC[A/G]GGCGTGGTGGCGGGC	4703
rs145480296	snp	A/G	0.00304185	0.0388803	intron-variant	NEB	GRCh38.p7	2:151547566	CCCCAAAACATATGT[A/G]TTAGAGACCGAATGA	4703
rs145487424	snp	A/C	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151610954	CATTACAGTTGTTAG[A/C]AAATTTAACTCACAT	4703
rs145516449	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151552616	TTTTGCCACCTCTGC[C/T]TGAGTGGTGGCCCTG	4703
rs145541944	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151691265	TTCTCTCCTTAGGCC[A/G]TTCTTCCCTGCTGCT	4703
rs145603467	snp	A/T	0.000798403	0.0199641	intron-variant, utr-variant-3-prime, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151498096	AGATGAAGTAAAAAA[A/T]TGACATTAACTGTAT	4703
rs145632757	snp	A/G	1.65693e-05	0.00287826	missense	NEB	GRCh38.p7	2:151666151	GCATCGGGCAGGAGA[A/G]TGTAGTGGTGGTATG	4703
rs145636096	snp	C/G	0.00584632	0.0537492	intron-variant	NEB	GRCh38.p7	2:151547413	TACTCCAGAAAGACC[C/G]CTACGAGATGCTTAC	4703
rs145666661	snp	A/G	0.0209421	0.100162	intron-variant	NEB, RIF1	GRCh38.p7	2:151520291	AACTTGGCCAAAAAT[A/G]GTATAACTCCTGAGT	4703
rs145672571	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151512368	AGTCTCACCCTGTCA[C/T]CCAGGGGACTGCAGT	4703
rs145679681	snp	G/T	0.00398564	0.0444627	intron-variant	NEB	GRCh38.p7	2:151709303	TTCTCCTTCTAAACA[G/T]CAAAAGGCCCTTCCA	4703
rs145747570	snp	G/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151532405	AAAGGCATTTTTCCA[G/T]GTCAAAGATGAAACA	4703
rs145769840	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151682960	TGCTTTCCTTCTAAC[A/T]GGCGTTATGTTCCAT	4703
rs145770770	snp	A/T	0.0218439	0.10221	missense, intron-variant	NEB	GRCh38.p7	2:151631294	ACATCCATAGACCCA[A/T]TGGGGACCCAGCCAA	4703
rs145791975	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151509660	TTGAGGCGGAGTTTC[A/G]CAGTGTCTCCAGGCT	4703
rs145806704	snp	A/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151486117	CAAGTCATGTATCTG[A/T]TAGGCAATTAATATC	4703
rs145812321	snp	A/G	0.00636936	0.0560724	intron-variant	NEB, RIF1	GRCh38.p7	2:151525784	TAATTGCCAGAATTG[A/G]AAAGCCAATAAATAC	4703
rs145828929	snp	G/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151638395	TGTGAGGAATGCCCC[G/T]CAGCTTGGGATATTG	4703
rs145833677	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151598545	TTGTGATCATAAGTT[A/G]AAGTCGTGAGTGCTA	4703
rs145900263	snp	C/G	0.00358779	0.0422022	intron-variant	NEB, RIF1	GRCh38.p7	2:151513868	GTGGTGTCTTCAGAA[C/G]CCCTCTGGAGGAAAC	4703
rs145934092	snp	C/T	0.0402882	0.136092	intron-variant	NEB	GRCh38.p7	2:151718132	TGCTGGGATTACAGG[C/T]GTGAGCCACCGCGCC	4703
rs145934392	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151489860	ATAAAAGAGCATTAT[A/G]TAAAATAGAAGGTTT	4703
rs145982188	snp	A/G	0.00159617	0.0282053	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151495272	GGAAATGACATTGAA[A/G]AGGAAGAATTCTGTT	4703
rs145984054	snp	A/C	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151578034	GAAACTGTCTTAAAT[A/C]TACCACTTGGCAATG	4703
rs145999882	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151704714	TGCCTCGCCCTGCTT[C/T]GGCTCACGCACAGTG	4703
rs146019317	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151560439	GCACATAGACTCTAA[C/T]GACTGAGCATTTGGA	4703
rs146033860	snp	C/T	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151657168	GCCAAATTACTCCAG[C/T]GTAATAGAGGGGAGA	4703
rs146034002	snp	C/G	0.00438332	0.0466095	intron-variant	NEB	GRCh38.p7	2:151708001	AAACTTTACTCTCCC[C/G]CTACCCGCATCTGGG	4703
rs146054669	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151629021	TTCCTCGTCTTTGTC[C/T]TTCTGTTTTCATTTT	4703
rs146055982	snp	A/C	0.00279162	0.0372561	intron-variant	NEB	GRCh38.p7	2:151554507	GAGGCTTGCAGTGAG[A/C]TGTGATTGCACCACT	4703
rs146068676	snp	C/T	0.0225045	0.103662	intron-variant	NEB	GRCh38.p7	2:151702955	GTTTCTTCCTAGTCT[C/T]GATGGTCTTTACATT	4703
rs146070001	in-del	-/A			intron-variant	NEB	GRCh38.p7	2:151550267	GGAGACCCTGTCTCC[-/A]AAAAAAAAAAAAAAA	4703
rs146070062	snp	A/C	0.107341	0.205301	intron-variant	NEB	GRCh38.p7	2:151576477	ATAAAATATATATAA[A/C]ATAAATACATATATA	4703
rs146086195	snp	A/G	0.00398564	0.0444627	intron-variant	NEB	GRCh38.p7	2:151678901	GACATTTGTTATTCA[A/G]TCATCACATATTTAC	4703
rs146106959	snp	A/C	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151560299	GTATTATGTCTTCAG[A/C]CCATCCTTACTTCTG	4703
rs146122727	snp	A/G	0.00795532	0.062565	intron-variant	NEB	GRCh38.p7	2:151682414	AAATGAATGGTTAAC[A/G]TAAATGGTTAACAAG	4703
rs146153331	snp	C/T	0.387832	0.208572	intron-variant	NEB	GRCh38.p7	2:151595034	TTTCCTATGTTTGGA[C/T]AACATAGGCAAGTTT	4703
rs146156804	snp	C/T	0.0138972	0.0823475	intron-variant	NEB	GRCh38.p7	2:151637538	GAGCGCCCATGGCAG[C/T]GTCCCAGTCTGGGTG	4703
rs146169352	snp	A/T	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151674729	GGCAAAGTGTCACAC[A/T]GTGTGTAGCATGAGA	4703
rs146176320	snp	G/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151531675	ACATCTCGCACCCCT[G/T]CCTCCCTCCCACTAA	4703
rs146178064	snp	A/T	1.8085e-05	0.00300702	missense, intron-variant	NEB	GRCh38.p7	2:151609812	CATGTTACGTACATC[A/T]CTCTGCAGGTCATAG	4703
rs146190536	snp	C/T	0.00438332	0.0466095	intron-variant	NEB	GRCh38.p7	2:151681938	CACATATCCCCCAAC[C/T]GGTGAAGCAATAATA	4703
rs146227449	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151535468	GGTGCTGATGTTTGC[C/G]GGGCTCTCCCACCAC	4703
rs146257939	snp	G/T	0.0162398	0.0886349	intron-variant	NEB	GRCh38.p7	2:151572298	CTGTACTCCAGCCTG[G/T]GTGACAGAGCAAGAC	4703
rs146263790	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151625062	ACATTAAAGTTTATT[A/C]AACAAATACTTTGCA	4703
rs146278361	snp	C/T	0.00517822	0.0506191	intron-variant	NEB	GRCh38.p7	2:151695398	TTACTTATAAGATTG[C/T]TACACATATTTTGTA	4703
rs146294986	snp	A/G	0.00200783	0.0316209	synonymous-codon	NEB	GRCh38.p7	2:151562641	CTGGGCGTTTCGGAC[A/G]CGTATAACATTGGGT	4703
rs146295003	snp	A/G	0.00478085	0.0486577	intron-variant	NEB, RIF1	GRCh38.p7	2:151511566	TCCCCAGGTGCCTAT[A/G]AAGCACAGCTAGGGC	4703
rs146310692	snp	C/T	0.00179736	0.0299241	missense	NEB	GRCh38.p7	2:151662137	TTGAAAGACTTACTT[C/T]GTTCATAATTTTTGC	4703
rs146323641	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151589817	TACGTACAGAGAGTT[A/G]TGTTTTCAGAGCATT	4703
rs146347370	snp	A/G	0.00318978	0.0398085	intron-variant	NEB	GRCh38.p7	2:151720230	AATAAGGAAAACATG[A/G]TAAGTAGATTAAGAA	4703
rs146383966	snp	A/T	0.02016	0.0983543	intron-variant	NEB	GRCh38.p7	2:151578365	GCCCTTCTTTGATTC[A/T]TAGCTGAAGGACCAT	4703
rs146387362	snp	A/G	0.00478085	0.0486577	intron-variant	NEB, RIF1	GRCh38.p7	2:151487732	GTTTTAGGTCAAATG[A/G]CATGTGTGTTTAAAC	4703
rs146397445	snp	G/T	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151677227	CTGCCACAATAAAGT[G/T]TCTGGGATTTAAGCT	4703
rs146460133	snp	A/G	0.00204114	0.0318811	synonymous-codon	NEB	GRCh38.p7	2:151692278	CACTGAAGTTCTTCA[A/G]CTGAGTATCAAGTTG	4703
rs146484052	snp	C/T	0.0138799	0.0821421	intron-variant	NEB	GRCh38.p7	2:151552119	TGGCGGGATCTGATA[C/T]TGACTTACCAACCTG	4703
rs146497640	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151649674	ATTATGTGCTAGATA[C/T]TGGTGTCAGAGCTGG	4703
rs146497711	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151695855	GACACTTGGCAGCTA[C/T]TATCACATCTGTCAC	4703
rs146506218	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151507205	AATTTTAAAAAACAT[A/G]TAAAGCTAGGGGTTT	4703
rs146517474	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151556000	CCAAGAATCTTGCCT[C/T]TATAATTTTGTTCAT	4703
rs146518636	snp	C/T	0.000798403	0.0199641	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151503105	CATTAAGTTATATAA[C/T]GCTGAGGAATCTTGT	4703
rs146583317	snp	C/T	0.0221141	0.102801	intron-variant	NEB	GRCh38.p7	2:151673018	TTTCATAGGGTTTCA[C/T]AGGTTTCGATTTAAT	4703
rs146604424	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151529367	ATAGCAGCATACTGA[A/G]CATCTTAAAAAACAA	4703
rs146605251	snp	A/C	0.0154538	0.0865337	intron-variant	NEB	GRCh38.p7	2:151634804	TCATTTTGAAAACTG[A/C]TTGTACTTGTAAAAC	4703
rs146606674	snp	A/C	0.00199481	0.0315187	intron-variant	NEB, RIF1	GRCh38.p7	2:151491623	GCCCAAATGAAAGTC[A/C]TTGACTCTAGCATAC	4703
rs146616621	snp	C/T	0.0042476	0.0458885	missense	NEB	GRCh38.p7	2:151677746	ATGCCTTTCATCCAG[C/T]TGTTGTAGTCTTCCT	4703
rs146616669	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151631564	AGGTTATTAGGAGAG[A/G]AGTGATCCCAAGTAA	4703
rs146637177	snp	A/G	5.55612e-05	0.00527044	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151531828	TTTTGTAGTACGCAG[A/G]TGTTCTGGAGTATCC	4703
rs146688470	snp	C/T	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151733263	ATGACATTATAAAAA[C/T]AGAATTTGAAGCTAA	4703
rs146701316	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151654729	TAGGCACTTTTATGG[A/T]CCCAATTTTAGGGAT	4703
rs146724879	snp	A/G	0.039522	0.134904	intron-variant	NEB	GRCh38.p7	2:151616883	CTATTATCTCGGACA[A/G]TGATTCATATATGGA	4703
rs146736340	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151611632	TTGGATAAAAATAGA[C/T]TGATAAAATTTTGGA	4703
rs146743760	snp	C/G	0.135825	0.222405	intron-variant	NEB	GRCh38.p7	2:151697848	GAGGCGGGCGGATCA[C/G]GAGGTCAGGAGTTTG	4703
rs146747679	snp	A/T	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151551524	TTGTAAATATTGCTA[A/T]AACATGCCCATTATG	4703
rs146809070	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151712936	CCAAACTCTGTTGTA[C/T]TTGCAGTTGAACGAT	4703
rs146843924	snp	A/T	0.00622694	0.0554499	intron-variant	NEB	GRCh38.p7	2:151570049	CATGGCAAACTGAGA[A/T]AAGAGTTCAACCCCA	4703
rs146858921	snp	A/G	0.00358779	0.0422022	intron-variant	NEB	GRCh38.p7	2:151716995	CCACTGCTGTTAACT[A/G]AGCTATGTCTGAGAC	4703
rs146859476	snp	C/T	0.0130921	0.0798413	intron-variant	NEB	GRCh38.p7	2:151668919	TTTAATGTGGAGGCT[C/T]AGGGTCCACACTGAA	4703
rs146867570	snp	A/C	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151528661	GTTTCATTGTATAAC[A/C]ATTTAATATATTTTT	4703
rs146878975	snp	C/T	0.00199481	0.0315187	intron-variant	NEB, RIF1	GRCh38.p7	2:151525471	CCACCTGGCAATCTT[C/T]GGAGAACCTGGGTAG	4703
rs146893231	snp	A/G	0.00953873	0.0683987	intron-variant	NEB	GRCh38.p7	2:151557711	ATGCAAGCCTGGTTC[A/G]ACATATGCAAATCAA	4703
rs146894367	snp	C/T	0.00636936	0.0560724	intron-variant	NEB	GRCh38.p7	2:151659273	TTCATGTATTTTTAT[C/T]AGCTAGGTTTAAATT	4703
rs146904441	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151655203	ATATCAGTATTTACT[A/G]TTACATTATTTTATA	4703
rs146904996	snp	C/T	0.00318978	0.0398085	intron-variant	NEB	GRCh38.p7	2:151706388	ATCCCAAGCCCAGTC[C/T]CGTTTGCCTAATATG	4703
rs146930335	in-del	-/CATT			intron-variant	NEB, RIF1	GRCh38.p7	2:151502427	CAAACATAAAGAATA[-/CATT]AAACAGCCACAATAA	4703
rs146954746	in-del	-/C			intron-variant	NEB	GRCh38.p7	2:151723746	GACTCTACCTGCCTT[-/C]TTTGTTTTTTTTTTT	4703
rs146997299	snp	C/T	1.65963e-05	0.0028806	intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151534334	TCTGCTCAAACATCA[C/T]AGCATATTATAGCAA	4703
rs147000720	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151639203	CTTTCTAAAGCTGTC[A/G]TTTGGTATCATGTCA	4703
rs147010381	snp	G/T	0.00478085	0.0486577	intron-variant	NEB	GRCh38.p7	2:151683658	GAAAACAGTATGGTG[G/T]TTCCTCTACAAATAA	4703
rs147020028	snp	A/G	0.00358779	0.0422022	intron-variant	NEB, RIF1	GRCh38.p7	2:151530693	AGGGGTTCCTGTCTC[A/G]TCTACACAATAGCCC	4703
rs147022587	snp	A/T	0.0150606	0.0854603	intron-variant	NEB	GRCh38.p7	2:151635790	TCTTTTCATAAGGGC[A/T]AATTTCAATAGCAAG	4703
rs147042788	snp	C/G	0.00318978	0.0398085	intron-variant	NEB, RIF1	GRCh38.p7	2:151530007	AGTCTTGCTCTCCTT[C/G]TGTGCTCCGGCAGTT	4703
rs147071904	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151533769	ATGGGGAATGATACA[A/G]CTAGTTTCACTTACG	4703
rs147084767	snp	C/T	0.0146672	0.084371	intron-variant	NEB	GRCh38.p7	2:151659335	AGAGTCTTGCGCTGT[C/T]ACCCAGGCTGGAGTG	4703
rs147095816	in-del	-/AC			intron-variant	NEB	GRCh38.p7	2:151709351	CAAATTGATAAATGT[-/AC]AGTTTGGTTCCTCAG	4703
rs147104220	snp	A/G	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151622673	CTTGAATACTTTACC[A/G]TGTATCTCCTAAGAA	4703
rs147106649	snp	A/T	0.000155684	0.00882143	intron-variant	NEB	GRCh38.p7	2:151551724	CTGGGCACTCTCAAG[A/T]TCTCACTGCTCACCG	4703
rs147126799	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151618136	AGTATCACTAAGTAA[C/T]TATGGTATTATAGTG	4703
rs147159176	snp	C/T	0.0025866	0.0358693	missense	NEB	GRCh38.p7	2:151563872	ACAATGGGAATGTAG[C/T]GCTCATCCAGGGTGT	4703
rs147168910	snp	C/G/T	0.0019193	0.0309191	missense, intron-variant	NEB	GRCh38.p7	2:151633929	GGGCTCCAATATGGT[C/G/T]GCCAAGTTGCTTGCA	4703
rs147170347	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151711003	TAACGAATAGATCTT[C/T]GCCTTTAGAGTTAAA	4703
rs147188964	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151567869	AAGGGGGGTGGTGGG[C/T]GGGTGAAGAAACAAG	4703
rs147200342	snp	A/G	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151714186	ATCTGTCTAAGGTCC[A/G]GACCTACCAAAGAAG	4703
rs147208822	snp	C/T	0.0023933	0.0345097	intron-variant	NEB, RIF1	GRCh38.p7	2:151526701	TCTGCTGGTGCAGTA[C/T]AAATCGAGGACTGTC	4703
rs147255671	snp	C/G	0.00358779	0.0422022	intron-variant	NEB	GRCh38.p7	2:151731856	CAGTGATATTTCTGA[C/G]CCTTAGGTACATAAG	4703
rs147262394	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151545007	GCCAAGGCACTATGG[A/G]ACACATGTAAATAAC	4703
rs147275999	snp	G/T	0.00318978	0.0398085	intron-variant	NEB	GRCh38.p7	2:151689733	CTGTGACCACATACA[G/T]CACTGTATTTCTCTG	4703
rs147292884	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151549855	ATACTTAATACACTT[A/G]TGCTCACTGAATTGA	4703
rs147296452	snp	C/T	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151651583	TCCACAGGAGCTCAA[C/T]ATACTGCCAAATGGG	4703
rs147305883	snp	C/T	0.0021838	0.0329717	missense	NEB	GRCh38.p7	2:151694363	AAGGAGTGCAGCATC[C/T]TGGGATCGTCATTAA	4703
rs147306586	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151646999	GGATTCCCAAAAGGA[C/T]TTTTTGGGGGGGAAT	4703
rs147313132	snp	A/T	1.65811e-05	0.00287929	intron-variant	NEB, RIF1	GRCh38.p7	2:151505609	GAAAGGTATTATTAC[A/T]TGCTGGACTGTTATT	4703
rs147336598	snp	G/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151501036	GTGGCTTCAAGTCCA[G/T]TATCTTTTCTTGCAT	4703
rs147369976	snp	A/G	0.0221141	0.102801	intron-variant	NEB, RIF1	GRCh38.p7	2:151521792	GGCTCCCTTCTCCAT[A/G]GGAAGTCCTCTAAAC	4703
rs147371427	snp	A/G	0.0260105	0.111035	intron-variant	NEB	GRCh38.p7	2:151629819	AAAATACTATATAGC[A/G]TTAGAAATAAATGGG	4703
rs147381051	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151671739	CTGTCCACCTAGGCT[A/G]TGCTTGAGCTCATCT	4703
rs147399704	snp	C/T	0.00199481	0.0315187	intron-variant	NEB, RIF1	GRCh38.p7	2:151527179	TCACTGCATTTTGGA[C/T]TCCTCCTTTTCAGCC	4703
rs147400784	snp	C/T	0.00438332	0.0466095	intron-variant	NEB	GRCh38.p7	2:151632873	TGACATCAACCCTTT[C/T]AAACTATCTTTTCTG	4703
rs147474831	snp	A/C	0.0209421	0.100162	intron-variant	NEB, RIF1	GRCh38.p7	2:151501826	TAAATTAGGGAACCA[A/C]AGAAAGAGGAGAGAG	4703
rs147475315	snp	A/C/G	0.000663763	0.0182057	intron-variant	NEB	GRCh38.p7	2:151610671	GAGTGTTTGAGGAAG[A/C/G]TAATAGGCCAATTCC	4703
rs147476634	snp	A/G	0.00019884	0.00996898	missense	NEB	GRCh38.p7	2:151656370	GATTGCATCTTAGCC[A/G]CTTGCATGGAATGGA	4703
rs147485418	snp	C/T	0.00398564	0.0444627	intron-variant	NEB	GRCh38.p7	2:151652627	CTTTATGTTATCTTC[C/T]GACTCTAAATTCTAT	4703
rs147488015	snp	G/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151730255	GTCCTAAACAGAGTG[G/T]TGCTAATATGAAAAC	4703
rs147504759	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151505924	GTTCTTTGACTGTAC[C/T]GGATTCTACCTTCTC	4703
rs147507059	snp	C/T	0.0263992	0.111815	intron-variant	NEB	GRCh38.p7	2:151613827	CTTCACCTTCCACCA[C/T]GATTGTAAGTTTCCT	4703
rs147518393	snp	A/G	0.00795532	0.062565	upstream-variant-2KB	NEB	GRCh38.p7	2:151735126	CAAGCTGCTAGGAAT[A/G]CAGAACCTCTCTCAT	4703
rs147560108	snp	A/T	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151630344	CTTTTCTGCCCCTTT[A/T]CTCTCTCTGCCCTGG	4703
rs147569843	snp	A/G	0.0152254	0.085912	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151627011	GCTCACCTTGTTCAT[A/G]TTGAGAGCATTGTTC	4703
rs147573063	snp	A/G	0.00438332	0.0466095	intron-variant	NEB	GRCh38.p7	2:151705506	ACAGCCACCATGGAA[A/G]ACAGTATGGAGATTC	4703
rs147579763	snp	A/G			synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151603727	CAGAACCCTCTGGCA[A/G]CCATCCAATACCCTT	4703
rs147589464	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151561178	ACAAGAAATAGTTTG[C/T]CCCTGGAAGAGGAGT	4703
rs147635867	snp	C/T	0.00358779	0.0422022	intron-variant	NEB	GRCh38.p7	2:151718043	TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGC	4703
rs147654864	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151686896	AGGCAAAAGGCATGA[A/G]AAGAAATGTTCATTT	4703
rs147664385	snp	C/T	0.00795532	0.062565	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151533935	ACTCAATCTGCAGTT[C/T]ACAGTTGCAGTTTTC	4703
rs147676904	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151683172	AAGGTGGGTTATTTG[C/T]TCATTTTCTAATTTC	4703
rs147693870	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151539736	CAGCCTTGCCCTCGA[C/T]TGTGTGATATGGAAA	4703
rs147769181	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151513975	AGTATAAAGTAAATT[A/G]TACATCTAGTTTGGT	4703
rs147771348	snp	C/T	0.000189316	0.0097274	intron-variant	NEB	GRCh38.p7	2:151667940	GAGGTTATTTTATTA[C/T]TTGACATCATTAAAA	4703
rs147771455	snp	G/T	0.0107246	0.0724382	intron-variant	NEB	GRCh38.p7	2:151622106	CCCAGGTTCAAGCGA[G/T]TCTCGTGCCTCAGCC	4703
rs147781115	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151664329	CTTACATTAAATAAT[G/T]AACAGATGATTAGAG	4703
rs147799407	snp	C/G	0.00636936	0.0560724	intron-variant	NEB, RIF1	GRCh38.p7	2:151518517	TTACACAGCACCATT[C/G]TCAAGATCAAACTAA	4703
rs147800947	snp	C/T	3.31934e-05	0.00407377	intron-variant	NEB	GRCh38.p7	2:151626963	GTATCTTGAATGACA[C/T]ATAGCCCTGTCTTAT	4703
rs147836259	in-del	-/TT	0.00318978	0.0398085	intron-variant	NEB, RIF1	GRCh38.p7	2:151515138	TTCAGGCTGAGACAC[-/TT]TGATGGGCCCCTCAC	4703
rs147846081	in-del	-/A	0.350982	0.228698	intron-variant	NEB	GRCh38.p7	2:151633377	GTTTCTTCCTTCCTT[-/A]AAAAAAAGAATAAAT	4703
rs147856812	snp	C/T	0.00478085	0.0486577	intron-variant	NEB	GRCh38.p7	2:151726280	ATGTATGGCAATATA[C/T]TGACAAAAAATTCTA	4703
rs147872436	snp	C/G/T	0.000298454	0.0122126	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151491692	ACACACCATTAATCA[C/G/T]GTGTAAGCTTCGGGA	4703
rs147875484	snp	A/T	0.0103295	0.0711199	intron-variant	NEB	GRCh38.p7	2:151575354	TATTTTTACAAAGAC[A/T]TCTCATAATTATTTT	4703
rs147885742	snp	C/T	0.0155376	0.0867604	intron-variant	NEB	GRCh38.p7	2:151642907	ACTGGTATAGGCCAG[C/T]AATAAATAGACACAT	4703
rs147972500	snp	A/G	0.00795532	0.062565	intron-variant	NEB	GRCh38.p7	2:151719623	GGCACAGTGACTCAC[A/G]CCTGTAATCCCAGCA	4703
rs147993604	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151734335	CTTTGAAAAATACTT[C/T]GAGGGAAGTTGTGGA	4703
rs148024760	snp	A/C	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151714000	CTCCCTAGTATAATG[A/C]GTATTTTGAATTAAA	4703
rs148029966	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151587141	ATATGAGGTCAACAA[A/G]TATTTGTGTTCCTGA	4703
rs148033771	snp	A/C	0.0111196	0.0737302	intron-variant	NEB	GRCh38.p7	2:151607313	TCTAGGCACCCACCG[A/C]TGTATCCAAGCACTC	4703
rs148054269	snp	A/G	0.00438332	0.0466095	intron-variant	NEB	GRCh38.p7	2:151670342	TCTCTTTCTGGTGGA[A/G]GCATTTTAACAGAAC	4703
rs148062318	snp	A/G	0.00199481	0.0315187	intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151534427	GTCATCTCTAGTGGC[A/G]GGCTCCCAACATACC	4703
rs148095660	snp	C/T	0.012368	0.0776596	synonymous-codon	NEB	GRCh38.p7	2:151562719	GTCACTGAGGATGTA[C/T]TGGCACCTTTTAGCC	4703
rs148107832	snp	A/G	0.0174175	0.0916809	intron-variant	NEB	GRCh38.p7	2:151706728	TACTCAGAGGGACTC[A/G]TGCCTTTCTGTGGTT	4703
rs148151643	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151659824	ATAGGTTAGACATAT[A/T]TGAACCTTCTTAAAA	4703
rs148184489	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151680995	GCAATACAAAAGTCA[A/G]TATCTTTAAAAATCC	4703
rs148203573	snp	C/G	0.039522	0.134904	intron-variant	NEB	GRCh38.p7	2:151617849	GGTGGATCACCTGAG[C/G]TCAGGAGTTTGAGAC	4703
rs148205046	snp	C/T	0.00636936	0.0560724	intron-variant	NEB	GRCh38.p7	2:151692956	GCCTGGATGACAGAG[C/T]GAGAGCCTGTCTCAA	4703
rs148214232	snp	C/T	0.00795532	0.062565	intron-variant	NEB	GRCh38.p7	2:151636712	CTTGAACCTGGGAGG[C/T]GGAAGTTGCAGTGAG	4703
rs148233755	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151644835	ACAAAGATACATTCC[A/G]AGAAATGTATTGTTA	4703
rs148245892	snp	C/T	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151541987	CTCAGCCAAGTTGCC[C/T]GTGTTTCTTCTTTGC	4703
rs148268080	snp	A/C	0.00755907	0.0610114	intron-variant	NEB	GRCh38.p7	2:151710174	ACTAATCTCACTTTG[A/C]AGTCAGTAAGAGGGT	4703
rs148275764	snp	C/T	0.00119737	0.0244387	intron-variant	NEB, RIF1	GRCh38.p7	2:151493951	TGGGGGGAAATGTTA[C/T]GTTTAATCTATTACT	4703
rs148278920	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151632531	AAATACAAAAAATTA[C/G]TGGGGCAGGGAGGCA	4703
rs148330973	snp	A/C/G	0.00517822	0.0506191	intron-variant	NEB	GRCh38.p7	2:151665745	GAAATCCTGACCCAG[A/C/G]AATTCCTTTAACAAG	4703
rs148351995	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151729277	AAAGCCAAGGCTCCT[C/T]GGCTTGTTGTCACCA	4703
rs148357666	snp	G/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151516153	GTGTGGAGGGAACTT[G/T]TCATTCATAAAGGAA	4703
rs148359911	snp	G/T	0.0260105	0.111035	intron-variant	NEB	GRCh38.p7	2:151623828	CATATTTTAAAAATG[G/T]TATAAGTGGGAAAAA	4703
rs148426626	snp	C/G	0.00438332	0.0466095	intron-variant	NEB	GRCh38.p7	2:151708720	TGTGGATGTCTAAAA[C/G]GCATCTCAAATCTAC	4703
rs148435739	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151573112	GTGCTTTCTAAATAA[C/T]GGCAGCAGTTTTAAA	4703
rs148442805	snp	A/G	0.00159617	0.0282053	intron-variant	NEB, RIF1	GRCh38.p7	2:151512540	GCTGATCTCAAACTC[A/G]TGGACTTAAATGATC	4703
rs148455519	snp	A/G	0.0014457	0.0268469	intron-variant	NEB	GRCh38.p7	2:151663533	AAACGCTCTGCAAAT[A/G]TGGTTTTCACGTACA	4703
rs148465926	snp	A/C	0.00755907	0.0610114	intron-variant	NEB	GRCh38.p7	2:151560818	CTAACTCCCAGGACT[A/C]CTCTTTAAGGTGGGG	4703
rs148497574	snp	C/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151550908	CCATGACCTCCTAAA[C/G]TGCTGGGATTACAGG	4703
rs148501384	snp	A/G	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151683062	GCTGCACTTCAAAGA[A/G]TAAGTGAAATTGTCA	4703
rs148505154	in-del	-/A			intron-variant	NEB	GRCh38.p7	2:151555872	TAAAAAAAAAAAAAA[-/A]CACATACACACACAC	4703
rs148508525	snp	A/G	0.00874735	0.0655527	intron-variant	NEB	GRCh38.p7	2:151695121	AGTTTGAAAAATGAA[A/G]GATAGAAATGGGTAT	4703
rs148527227	in-del	-/T/TT	0.0795561	0.182899	intron-variant	NEB	GRCh38.p7	2:151733101	AGTTTGCTGTCAGTG[-/T/TT]TTTTTTTTTTAAATC	4703
rs148540062	snp	A/T	0.0221141	0.102801	intron-variant	NEB, RIF1	GRCh38.p7	2:151501836	AACCAAAGAAAGAGG[A/T]GAGAGAGAGACAGGT	4703
rs148550869	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151646847	TAGAAACAGGGTTTC[A/G]CTACGTTGTGCAGGC	4703
rs148580196	snp	A/G	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151578842	ATCCCAGAACTTTGG[A/G]AGGCTGAGACGGGTG	4703
rs148581337	snp	C/T	0.0115144	0.0749975	intron-variant	NEB	GRCh38.p7	2:151634616	CACTGCACTCCAGCC[C/T]GGGTGACAGCAAGAC	4703
rs148583515	snp	A/G	0.00755907	0.0610114	intron-variant	NEB	GRCh38.p7	2:151711738	TTAATAAGATCATTC[A/G]CTAAAGAGTGCTTTG	4703
rs148589314	snp	C/T	0.00279162	0.0372561	intron-variant	NEB, RIF1	GRCh38.p7	2:151495950	TACTCCACCACCCCA[C/T]ACGTACCCGTCCTAA	4703
rs148612471	snp	C/T	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151630423	GTGGGCATGAATATT[C/T]TGGCAGAAATAATGG	4703
rs148641869	snp	A/C	0.0295035	0.117819	intron-variant	NEB, RIF1	GRCh38.p7	2:151531360	CTCACTTTGCCACCC[A/C]GGCTGGAGTGCAGTG	4703
rs148653052	snp	C/T	0.00676609	0.0577691	intron-variant	NEB	GRCh38.p7	2:151556216	TCTAAGCTGTGCATC[C/T]GTAAGCCCAGTAGAG	4703
rs148677492	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151626155	GTTTCACTCTCTTGC[C/T]CAGGCTGGAATGTAG	4703
rs148705319	snp	A/G	0.0023933	0.0345097	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151506687	CCCTGGGATTAAAAA[A/G]TTTAAAAATAAAAGT	4703
rs148706867	snp	C/T	0.0170251	0.090679	intron-variant	NEB	GRCh38.p7	2:151615442	TAGAGAAGAGGCAAG[C/T]GGGTACTGAGAAAAA	4703
rs148729817	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151656951	AATTATGAGACACAC[A/G]GTGTAATTTTAGAAT	4703
rs148759106	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151610300	TGTAATGTAATCATA[C/T]ATCTTCATTGGTGAA	4703
rs148761280	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151685508	ACTGAGAATCTCAAA[A/G]GTTGTTTTCATATCA	4703
rs148761390	snp	C/T	0.00279162	0.0372561	intron-variant	NEB, RIF1	GRCh38.p7	2:151495082	ATCCTCTATGCTCTG[C/T]CTCTTGCTTTAGTTT	4703
rs148794372	snp	A/G	0.000115924	0.00761239	synonymous-codon	NEB	GRCh38.p7	2:151672519	AACCATGTCCCCAGG[A/G]GTATGGTAGCTGGTT	4703
rs148803532	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151537720	CCAAGTTGAAATTCA[C/G]TCACTTAGCAATTGA	4703
rs148814261	snp	C/G	0.000915751	0.0213784	intron-variant	NEB	GRCh38.p7	2:151552662	CTTAACTTCCCCAGT[C/G]ATCACTTACGTCACT	4703
rs148827640	snp	C/T	0.00478085	0.0486577	intron-variant	NEB	GRCh38.p7	2:151696509	TTTTATACAAATGTA[C/T]ACTGTTTAAACTTGC	4703
rs148837095	snp	A/T	0.000459116	0.0151442	intron-variant	NEB	GRCh38.p7	2:151565465	GACAATTTACTCCCC[A/T]GTCTGTGCACTTCAG	4703
rs148839798	in-del	-/A	0.00970376	0.0689762	intron-variant	NEB, RIF1	GRCh38.p7	2:151485949	TATTCGTGGGGATGG[-/A]AAAAGGGGAAATATT	4703
rs148843950	snp	C/T	0.0023933	0.0345097	intron-variant	NEB, RIF1	GRCh38.p7	2:151504729	TGCCTAGAATCTGCG[C/T]ATGGATGGGAAAAGG	4703
rs148857439	snp	C/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151654758	ATGAGGAAAGTGAGA[C/G]TTAGATAGGTAATTG	4703
rs148862132	in-del	-/A	0.000613034	0.0174969	intron-variant	NEB	GRCh38.p7	2:151665552	ATTCTTTACAATGAG[-/A]AAAAAAATTTCATTT	4703
rs148869778	snp	A/C	0.0170251	0.090679	intron-variant	NEB	GRCh38.p7	2:151648346	GAAGCCAATTAAGAC[A/C]CTCAGCACCCAAACA	4703
rs148890765	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151713931	TACCATCTGAACTGG[C/G]AGCTGTAAGAAAAGG	4703
rs148897243	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151498144	ATATCCTTTTGTAAT[A/G]TAAGATGTATTAGAA	4703
rs148899508	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151605476	GGATGGAAAGCAAGG[C/T]TGTGGCTTGAATCAG	4703
rs148910941	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151726815	AGGATCACCTGTGGC[C/G]AGGAGTTTACGACCA	4703
rs148950085	snp	C/T	0.000268156	0.0115761	intron-variant	NEB, RIF1	GRCh38.p7	2:151533439	CATCCCATCAGACAT[C/T]ACCTGGCTCCACATA	4703
rs148951113	snp	G/T	0.0134861	0.0810011	intron-variant	NEB	GRCh38.p7	2:151638438	AACCTGGGGTGAAGG[G/T]GGCAGGGGAGGCACC	4703
rs148976103	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151600182	TGACAGAGCAAGACT[C/T]TCCGTCTCAAAAAAA	4703
rs148983133	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151628229	ACCCAGAAATTTTAC[A/T]TATGATTTTGAGACT	4703
rs148985320	snp	A/G	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151706620	AAGCAACACATCCAT[A/G]TGGAGGCCCAGGTGC	4703
rs148992164	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151486645	AAGATCTGGTATATC[C/T]ATACAGATCTATTAT	4703
rs149025191	snp	C/G	0.0466329	0.14541	NEB	2	allele_origin=G(germline)/C(germline)	2:151617397	GTTGAGTTTGGCTAA[C/G]ATGATTTCTGGTGTA	4703
rs149080521	in-del	-/AGAAAGTAGTAGTT			intron-variant	NEB	GRCh38.p7	2:151675763	TTTTTATCCCTAGAG[-/AGAAAGTAGTAGTT]AGAATAAGTTTTTCA	4703
rs149089623	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151732866	ACGAATTAAAACCTG[A/C]CTTTACTCCAACTTG	4703
rs149111593	snp	G/T	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151674641	TTCCTCAACTGCTGG[G/T]ATTGTTTTGTTCTTT	4703
rs149132362	in-del	-/T			frameshift-variant	NEB	GRCh38.p7	2:151724281	AACATGGCGGTGTTC[-/T]TTAACGGCCTGGACA	4703
rs149160541	snp	A/G	0	0	intron-variant	NEB	GRCh38.p7	2:151575256	TGCTGTATGTTTTTT[A/G]GTTTTTTCTCCTTGG	4703
rs149162847	snp	A/G	0.00516398	0.0505502	synonymous-codon	NEB	GRCh38.p7	2:151678095	TTGTATCTTGGCCAC[A/G]TTCATATAATGAACC	4703
rs149194258	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151665177	ACTATGAAAGAGAAC[A/G]CTCTAAACATAATGG	4703
rs149204604	snp	A/C	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151529631	CGCCTCCCAGGTTCA[A/C]GCAATTCTCCTGCCT	4703
rs149259692	snp	A/G/T	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151718466	TCCCTACTCTCAGGG[A/G/T]CCAGTCTAAAACCCC	4703
rs149291452	snp	C/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151708531	ATGTTCCCATGGAAG[C/G]ACCCCAGAGCTCAGC	4703
rs149298863	snp	C/T	0.0221141	0.102801	intron-variant	NEB, RIF1	GRCh38.p7	2:151488436	CAGAGGGCTTGAGCC[C/T]AGGGGTTTGAGACCA	4703
rs149299471	snp	C/T	0.0236746	0.106192	intron-variant	NEB	GRCh38.p7	2:151572677	CAGCCACCCAAGTAG[C/T]TGGGATTACAGGTGA	4703
rs149302373	snp	A/C	0.0193772	0.0965046	intron-variant	NEB	GRCh38.p7	2:151629779	TTCTGGCAATAGTGG[A/C]AAGCAAATAAATTAT	4703
rs149351567	snp	A/G	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151526635	AATCATGGCGTTTCC[A/G]TAAAGAGTCCAGCCA	4703
rs149353499	snp	A/G/T	0.00954224	0.0684493	intron-variant	NEB	GRCh38.p7	2:151631987	AACCCCTGAAGCCCT[A/G/T]AGATCTTCAACAGCT	4703
rs149374507	snp	A/G	0.00279162	0.0372561	intron-variant	NEB	GRCh38.p7	2:151549961	ATAGAACAATGAGTG[A/G]AATGGTTTATTGAAA	4703
rs149384863	snp	C/G	0.000298186	0.0122067	missense, intron-variant	NEB	GRCh38.p7	2:151619588	CCAAAACGATACCAA[C/G]CATGTCCACTGGGCT	4703
rs149387872	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151695055	ACTCATTTATAGAAT[C/T]ATTGAAGAAATTGAG	4703
rs149396653	snp	A/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151558554	ACTTCAAACTATACT[A/T]CAAGGCTAAAGTAAT	4703
rs149429136	snp	C/T	0.0228947	0.104514	intron-variant	NEB	GRCh38.p7	2:151544827	TGGCCTGGAAGCCAA[C/T]GCTCAGCTGGGTGAA	4703
rs149430473	snp	C/T	0.000270265	0.0116215	missense, intron-variant	NEB	GRCh38.p7	2:151646225	TGTCCCAAGCTTCTC[C/T]ATAAAGTCTCTAAAA	4703
rs149471462	snp	C/G	0.000215312	0.0103735	missense	NEB	GRCh38.p7	2:151680765	TAATTTTAGACTGTA[C/G]TGTAATTGGAGCATC	4703
rs149510427	snp	A/G	0.0301101	0.118947	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151531078	TCTGGGTTTGGCCTT[A/G]TTGTATTCCAATTTA	4703
rs149515371	snp	C/T	0.00358779	0.0422022	intron-variant	NEB	GRCh38.p7	2:151667173	ATATTTCTATTTCCA[C/T]GGATTTTTTTTCTTC	4703
rs149553309	snp	A/G	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151520541	TTGAATGGAAGGAAG[A/G]GACAGTCATTATGTC	4703
rs149563358	snp	C/T	1.65825e-05	0.00287941	missense	NEB	GRCh38.p7	2:151567323	TATCAGCAGGTATAT[C/T]GATTTTGGCCTTTGT	4703
rs149596493	snp	C/T	0.000994546	0.0222774	missense	NEB	GRCh38.p7	2:151553904	ATCCATTCGTGGAGG[C/T]GCAGGCGGTAATCAA	4703
rs149598348	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151656908	TGAGAAATTATTCTG[C/T]CAGTCATTTACTGAT	4703
rs149606244	snp	A/G	5.88149e-05	0.00542254	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151514848	AGTTGCATATTTGAC[A/G]TGTAACAAAGCTGGC	4703
rs149636338	snp	C/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151501018	GAGCCACCATTTCTA[C/T]ATGTGGCTTCAAGTC	4703
rs149639365	snp	C/T	0.00283161	0.0375205	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151609992	CCACTTTTGGAATTC[C/T]TTCTTGTACTCCCTT	4703
rs149649421	snp	A/G	0.00517822	0.0506191	intron-variant	NEB	GRCh38.p7	2:151651577	GAAAATTCCACAGGA[A/G]CTCAACATACTGCCA	4703
rs149668769	snp	A/C	0.00199481	0.0315187	intron-variant	NEB, RIF1	GRCh38.p7	2:151528475	TGGATTTTGCAAGGT[A/C]CGTTTTACTGCATTT	4703
rs149672020	snp	C/T	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151634162	TGTAATTGTAGTATA[C/T]ACCCCAAATCACCTA	4703
rs149704259	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151621715	TCATTTGAGAACCAC[A/G]CATTAAACAAATCAT	4703
rs149734174	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151647985	GAAATACAGACGGAA[C/T]ATTTAGGCATCATGA	4703
rs149752325	snp	C/T	0.0118754	0.0761358	missense	NEB	GRCh38.p7	2:151560621	GCTTCTGGTTCTTGG[C/T]GTGTGTCAGGGACAA	4703
rs149757502	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151690950	CTTAGTTGATGCGTT[C/T]ATATTCTCACTTCTC	4703
rs149787815	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151682839	AAATCATCAAAGTTT[C/T]ACCCAAAACAATGTT	4703
rs149800451	in-del	-/AGC	0.0252325	0.109451	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151499075	TGTTACATTTGTAAA[-/AGC]AGGAATATAATACTG	4703
rs149840790	snp	G/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151676649	CTTTTCTACTGCTGT[G/T]ATATTGTTCCTTTTG	4703
rs149849735	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151597094	AATAGGGAATCAATA[C/T]CTGAAACATTAAGCC	4703
rs149881695	snp	C/T	0.0045643	0.0475533	missense	NEB	GRCh38.p7	2:151569306	GTTTGGCATGATTGA[C/T]GGACACGGAGTCATT	4703
rs149884361	snp	C/T	0.00358779	0.0422022	intron-variant	NEB	GRCh38.p7	2:151671899	TCTCCATGAATCATG[C/T]TGCAAGCACAAAACC	4703
rs149911633	snp	C/T	0.00636936	0.0560724	intron-variant	NEB, RIF1	GRCh38.p7	2:151523350	AATTCTAACTTGTTC[C/T]GTCACTTGACATTAC	4703
rs149916975	snp	C/T	0.00111255	0.0235593	intron-variant	NEB	GRCh38.p7	2:151658124	GGAAGAGTTTTCTTC[C/T]AAATATGAAAGCCTG	4703
rs149933044	in-del	-/CATACAGACGTGTCTCAGAATGAGA			intron-variant	NEB	GRCh38.p7	2:151670426	GAAAGAATAAGAGTC[-/CATACAGACGTGTCTCAGAATGAGA]CATACAGACGTGTCT	4703
rs149957861	snp	A/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151732378	TAAAATAAATATAAA[A/T]TAAATGATTAACAGC	4703
rs149965029	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151517391	CCCTACAGAAGACAC[A/G]AGGACGTTTCTAATA	4703
rs149968625	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151654335	CTGGTGGTATATTTT[A/G]TCATAGCTTCTGCTG	4703
rs149997606	snp	C/T	0.00478085	0.0486577	intron-variant	NEB	GRCh38.p7	2:151641959	CTAATGCTATCCCTC[C/T]TCCCTCCCCCCATCC	4703
rs150000214	snp	A/C	0.00318978	0.0398085	intron-variant	NEB	GRCh38.p7	2:151720509	GAATAGCAGGGAAGA[A/C]TTTACTTCATTATTG	4703
rs150007888	snp	C/T	0.00795532	0.062565	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151506310	GAAAAGAAAACCCAG[C/T]AGTTCCTGGAGAAAG	4703
rs150018403	in-del	-/G	0.00914312	0.0669923	intron-variant	NEB	GRCh38.p7	2:151696322	GAAATATCAGGCAGA[-/G]GGGGGGTTAAATCTT	4703
rs150039924	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151574824	GCAGCCTCTTCCTCC[A/T]GGGCTCAAGTGATCC	4703
rs150051588	snp	C/T	0.00318978	0.0398085	intron-variant	NEB	GRCh38.p7	2:151715125	TTCTGGCAATGCTTT[C/T]AAAGTACCCAACACT	4703
rs150106932	snp	A/G	0.00914312	0.0669923	intron-variant	NEB	GRCh38.p7	2:151684324	TCTGCAGAAAAAACC[A/G]TTATAAATATTTATG	4703
rs150135749	snp	A/G	0.000778152	0.0197097	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151640397	AGCATGGATGACGTC[A/G]CTCTGGTCGGGCAGG	4703
rs150145955	snp	G/T	0.0123036	0.0774623	intron-variant	NEB	GRCh38.p7	2:151534861	AGGGTTGTCCAGTCT[G/T]GAAATCTACTGAAAG	4703
rs150188635	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151673521	TGTATTTCATAGTGA[A/T]GTGCATTGTGTGCAG	4703
rs150203900	in-del	-/T			intron-variant	NEB	GRCh38.p7	2:151685794	TTGACCCACTGCCTT[-/T]CAGAAAACTCTAAAC	4703
rs150230249	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151526351	CAGTAGAACAGCAGC[A/G]TTGACAATACTAAAC	4703
rs150240848	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151668627	AGAGAAAGGCTAGTT[A/G]CATACAAAAAAAGAT	4703
rs150244233	in-del	-/A	0.146314	0.227484	intron-variant	NEB	GRCh38.p7	2:151655538	AACAAACTCAGATTT[-/A]AAAAAAAAATCTTTT	4703
rs150261574	snp	A/C	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151613667	TGTTGGAGGAGGGGC[A/C]TGGTGGGAGGTGATT	4703
rs150263820	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151688547	ACAGGATTCAAACTT[C/T]CATCCCCTATTTCAG	4703
rs150273794	snp	C/T	0.0023933	0.0345097	utr-variant-5-prime	NEB	GRCh38.p7	2:151734445	AAAGCCTCTCCCAAC[C/T]CTCCCCTCCTGAGAA	4703
rs150279580	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151519914	TGGGACATTTAGAGT[A/G]AAGAAGACACTATTA	4703
rs150283068	snp	A/G	6.62504e-05	0.00575507	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151627799	GGCTCCAATGTGGTG[A/G]CCGAGCTGCTTGCGG	4703
rs150315040	snp	C/T	0.0146672	0.084371	intron-variant	NEB	GRCh38.p7	2:151645079	AGTATGATTATGTTA[C/T]GGGACCACCGTCCTG	4703
rs150316683	snp	C/T	0.0174175	0.0916809	intron-variant	NEB	GRCh38.p7	2:151722485	GATAGCAAGAGCTCT[C/T]TGTGGGATAACTATA	4703
rs150322681	snp	C/T	0.00159617	0.0282053	intron-variant	NEB, RIF1	GRCh38.p7	2:151508901	TGATGATTGTTTTTA[C/T]TCTCTGCAGCAGAAC	4703
rs150355941	snp	C/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151494515	ATGAGAAACCACCAT[C/G]ATTTTACCGCTAGTC	4703
rs150397171	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151635340	TTGATTTTTAGAGCC[A/G]TCATTTGTTCCTCAA	4703
rs150399444	snp	G/T	0.00478085	0.0486577	intron-variant	NEB	GRCh38.p7	2:151713343	TCCCTGCAGAAAAGG[G/T]ATAAAGAACCCAGCT	4703
rs150405168	in-del	-/G	0.0107246	0.0724382	intron-variant	NEB	GRCh38.p7	2:151638428	TTTGAAGGTGAACCT[-/G]GGGTGAAGGTGGCAG	4703
rs150439727	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151566957	TTTTAAAAAAATTTG[A/G]TTGAAAGTTACTCAG	4703
rs150452058	snp	A/C/G	0.00676609	0.0577691	intron-variant	NEB	GRCh38.p7	2:151709152	GATTTATGAACCTGC[A/C/G]ACCAGGTTTTTTCAT	4703
rs150471104	snp	A/G	0.0123278	0.0775367	intron-variant	NEB, RIF1	GRCh38.p7	2:151514449	TCATGAAAGAAAAGC[A/G]ACAACATTGACAAGA	4703
rs150475192	snp	C/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151650983	TTTTTTTTGAGACAG[C/G]GGTCTATGTTTCCCA	4703
rs150494392	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151562020	CCTACACTGTTACAG[A/C]AACTTTCTTTGCCTG	4703
rs150496369	snp	C/T	0.000186251	0.00964836	synonymous-codon	NEB	GRCh38.p7	2:151664801	GGAGAGTAAAATATC[C/T]GGTGTGTCAGGCATG	4703
rs150504324	snp	C/T	0.00438332	0.0466095	intron-variant	NEB	GRCh38.p7	2:151544469	CAGTCTGGTGTGGAA[C/T]AAGGGGTCAGGGCCC	4703
rs150508438	snp	A/G	0.00597247	0.0543191	intron-variant	NEB	GRCh38.p7	2:151675933	ATGTTGTTACTTTAA[A/G]GAATTATATACACTT	4703
rs150518285	snp	A/G	0.00557542	0.0525036	intron-variant	NEB	GRCh38.p7	2:151720001	TTGAATAGGATAAAT[A/G]TTTATTAAGTATGAC	4703
rs150547862	snp	A/G	0.0162398	0.0886349	intron-variant	NEB, RIF1	GRCh38.p7	2:151527837	TGAAATGATTCTTCA[A/G]TCTCTCTAGTTCTGC	4703
rs150556274	snp	C/T	0.00478085	0.0486577	intron-variant	NEB	GRCh38.p7	2:151611431	TGTGGTTGCTGTTGA[C/T]GGATATAGTATAAAA	4703
rs150574827	in-del	-/G			intron-variant	NEB	GRCh38.p7	2:151689603	AGAACGGATGAGGCT[-/G]GTTTAATTTTGGAGC	4703
rs150590530	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151629479	CAAATGTTATAATAG[C/T]AATAATCCTGCCTCC	4703
rs150597695	snp	A/G	0.0244538	0.107838	intron-variant	NEB, RIF1	GRCh38.p7	2:151488143	TCCTATTTTGAGGGC[A/G]AGGGGAATAATTTAT	4703
rs150601326	snp	A/G	0.00318978	0.0398085	intron-variant	NEB, RIF1	GRCh38.p7	2:151521313	ATGCAGAACAGTTCA[A/G]CATGATGCAGGCACA	4703
rs150630968	snp	A/C	0.0209421	0.100162	intron-variant	NEB, RIF1	GRCh38.p7	2:151511119	ACATGCTGAAGCTTT[A/C]GTTAAAGATCAGCAG	4703
rs150641800	snp	C/T	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151660880	ATGGTAGAACCTAGC[C/T]ACATAGGCCGATTGA	4703
rs150716011	snp	A/G	0.00557542	0.0525036	intron-variant	NEB	GRCh38.p7	2:151636995	TGGGTGGGAGGGAAA[A/G]GCTTAACTGTTGATC	4703
rs150718757	snp	C/T	0.00676609	0.0577691	intron-variant	NEB	GRCh38.p7	2:151714810	AGAAAGAAGATATGA[C/T]CCTGCTGCAACATGG	4703
rs150746631	snp	A/G	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151568773	GACATGTGTGAACTG[A/G]GAAGATACACTAAAT	4703
rs150755583	snp	A/G	0.00159617	0.0282053	downstream-variant-500B, intron-variant	NEB, RIF1	GRCh38.p7	2:151485250	TTAGATAATTTTTTA[A/G]TAATTTTATGTACAA	4703
rs150770664	snp	C/T	0.00993419	0.0697739	intron-variant	NEB	GRCh38.p7	2:151710646	ATCTTCAGCAAGCCA[C/T]TCTTAGGTCCTTAAT	4703
rs150786947	snp	C/G	0.0209421	0.100162	intron-variant	NEB, RIF1	GRCh38.p7	2:151517012	GAGACCTGGGGTCTA[C/G]ATTGAATGGATAACA	4703
rs150799712	snp	A/G	0.0130921	0.0798413	intron-variant	NEB	GRCh38.p7	2:151666515	AATCTAGGTAACATC[A/G]AAGTTTTTTTTTGTA	4703
rs150833640	snp	C/T	0.00557542	0.0525036	intron-variant	NEB	GRCh38.p7	2:151690389	AATCGGAAATATTTG[C/T]CTTGTCCTACACAAA	4703
rs150842230	snp	A/G	0.00074599	0.0192987	synonymous-codon	NEB	GRCh38.p7	2:151553464	CCAGACGTAGCAACC[A/G]ATGCCTTTCAGCCAG	4703
rs150851976	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151624258	CAATGCATGATCATG[C/T]AATTTTAAAGAAAGT	4703
rs150874422	snp	C/G	0.000248573	0.0111456	missense	NEB	GRCh38.p7	2:151538181	GATGATAGACAATGT[C/G]TAGGGCATCTTTCAC	4703
rs150875491	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151641861	GGTACATGTGCACAA[C/T]GTGCAGGTTTGTTAC	4703
rs150886232	snp	C/T	0.00318978	0.0398085	intron-variant	NEB	GRCh38.p7	2:151686758	TCTCTAAACATTTTA[C/T]ACACAATATATACTA	4703
rs150893414	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151548955	TATTATTCCACCAGC[A/G]GCTCATTGTGGTCTG	4703
rs150950438	snp	A/G	0.00199481	0.0315187	intron-variant	NEB, RIF1	GRCh38.p7	2:151513468	CAGATGTTCAAGAAT[A/G]CCATTGTATGCATGT	4703
rs150961139	snp	A/C/T	0.000398186	0.014105	missense	NEB	GRCh38.p7	2:151663631	TATGGATCACGTTCC[A/C/T]GTAGTTGGCATTGGT	4703
rs150990450	snp	C/G	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151621369	TCCAAATTTGAATTG[C/G]GAACATTTTTACTAG	4703
rs150995303	snp	A/C	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151726867	CCTACCTCTATGAAA[A/C]AATAATTAGGAGATC	4703
rs151025761	snp	A/C	0.000392534	0.014004	intron-variant	NEB	GRCh38.p7	2:151717558	TGTATTTTAAAAACG[A/C]TTATGCTTTCATCTT	4703
rs151032458	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151502328	CCACTAAAGAACTTA[A/G]TAACCAAATACCACC	4703
rs151036013	snp	G/T	0.00716266	0.059414	intron-variant	NEB	GRCh38.p7	2:151639039	TAATAAAAGAAAATG[G/T]TCTACATAATCTCAT	4703
rs151044518	snp	C/G	0.0154538	0.0865337	intron-variant	NEB	GRCh38.p7	2:151653675	TAAAATAGACAAGTA[C/G]AAAGCAGTAAAATTA	4703
rs151065661	snp	C/T	0.00398564	0.0444627	intron-variant	NEB	GRCh38.p7	2:151571027	TCTTTTTTTTTGAGA[C/T]GGAGTTTCGCTCTTG	4703
rs151078091	snp	A/T	0.0174175	0.0916809	intron-variant	NEB	GRCh38.p7	2:151711985	CAGAAGTCAATAAAA[A/T]TGATTTCTGGATTTG	4703
rs151109510	snp	A/G	0.00597247	0.0543191	intron-variant	NEB, RIF1	GRCh38.p7	2:151519480	AGCTGACGGGAGGAG[A/G]GAATGGAGAGTTTTT	4703
rs151119873	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151565908	TTTTTTCAGAAGCTT[C/T]TAAAGGATTTCTCTC	4703
rs151120848	snp	A/G	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151668000	CTTATAAAACATGTC[A/G]TAATAGATCCCTTTC	4703
rs151150876	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151561931	AGGAGAGACTCAGAC[C/T]GGGAAGATCCAGCCC	4703
rs151190834	snp	A/G	0.0221141	0.102801	intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151507529	GCCAAAGACACAGAG[A/G]TACTAGGAGAATCTG	4703
rs151204359	snp	A/G	0.000345408	0.0131372	intron-variant	NEB	GRCh38.p7	2:151657936	AGCCCTTATTATTTC[A/G]GTTCCTTAGAAACCC	4703
rs151206071	snp	A/C	0.00296232	0.0383717	intron-variant	NEB	GRCh38.p7	2:151687547	CCTGCAAAGACATCA[A/C]ACATGCCAGATCCCA	4703
rs151236535	snp	A/G/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151678248	GCTTTACTAAACAAT[A/G/T]AGGCCATGATTTGAA	4703
rs151243988	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151545617	TTCTAATCTATAAAA[C/T]CATGCAAAACCCCTC	4703
rs151278908	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151634982	CAAAGACAACTGACC[A/G]AGAAAGTGTAGGTGA	4703
rs151332165	snp	C/T	0.00318978	0.0398085	intron-variant	NEB	GRCh38.p7	2:151708886	AAATCAAGTCAGCTG[C/T]GCTTTCAAAAGACTT	4703
rs151338614	snp	A/G	0.000449797	0.0149899	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151490380	CTTGTACCTGTTGAG[A/G]CTGCAAAGACACCCC	4703
rs180779260	snp	A/T	0.00038141	0.0138043	missense	NEB	GRCh38.p7	2:151710458	GTTATCAGCATTCAT[A/T]CTGGCATTTGCAACT	4703
rs180820209	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151565301	CAATAGAATAATTTG[A/G]ATAGGAATATAGATA	4703
rs180827597	snp	C/T	0.00636936	0.0560724	intron-variant	NEB	GRCh38.p7	2:151654720	CCAATGTCATAGGCA[C/T]TTTTATGGTCCCAAT	4703
rs180833976	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151726019	GGCAGATCTGAATTA[C/T]ATTCTGTAAATTTAG	4703
rs180841500	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151694792	TTCTTCTCAAGCTGG[A/G]GCTATTAATTCTCCA	4703
rs180844720	snp	C/G	0.00517822	0.0506191	intron-variant	NEB	GRCh38.p7	2:151634668	AAAATAAAATAAAAA[C/G]AGTAAAATGAGTGAC	4703
rs180847025	snp	A/C/G	0.00018219	0.00954281	missense, synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151627050	CACCTGCTCTAGAGA[A/C/G]TCAGTCACACTGGTA	4703
rs180855842	snp	C/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151532542	TTTAAGCAGGACAGA[C/T]ACAGAGAGCACCATA	4703
rs180857062	snp	C/T	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151645599	AGTCCTTCGTGGAAC[C/T]ACTTTAATACATTCT	4703
rs180857677	snp	C/T	0.00199481	0.0315187	intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151497191	CCGACTACTTTACTT[C/T]AGTGGAAGTTGTTGG	4703
rs180861698	snp	A/C	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151514162	ATTGAGGTATATTTT[A/C]TGTAATGGTTAACAA	4703
rs180861957	snp	C/T	0.00119737	0.0244387	intron-variant	NEB, RIF1	GRCh38.p7	2:151489147	CTTCCTTAAATATAA[C/T]AGGTCTAACACTTAT	4703
rs180864305	snp	A/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151676842	CTACATTCTTGTGAA[A/T]TTCTATATCCCATGA	4703
rs180867626	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151729969	TTTTTCTTATGGTCC[C/T]CAAGATAGAATTTGC	4703
rs180869338	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151556539	GGGCTAAGAATTACA[A/G]TAAAGCTTACAGGGA	4703
rs180881237	snp	A/G	0.000426519	0.0145972	synonymous-codon	NEB	GRCh38.p7	2:151687674	CAACAGGGGAATGGC[A/G]TCCACTTTAATGTCA	4703
rs180884188	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151573779	TAATTTCTGCGATCC[A/T]TGAAAATGGTATCTT	4703
rs180903156	snp	A/G	7.79636e-05	0.00624305	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151527556	CTTCCAGTGGGCTTT[A/G]TTGGCTTCGTACTGT	4703
rs180942330	snp	C/T	0.00119737	0.0244387	intron-variant	NEB, RIF1	GRCh38.p7	2:151507796	CCCCAATACCACCAA[C/T]GAAGTAACAGATGAG	4703
rs180950282	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151548022	TGAGTCAGACTAAAA[G/T]GCAACCTTATTAAAG	4703
rs181064751	snp	C/T	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151558847	AAAACCATAAAAACC[C/T]CAGAAGAAAACCTAG	4703
rs181075746	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151578082	ATGCTTTCCTGTAAT[A/G]AACTCATTCATTATA	4703
rs181077987	snp	G/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151494585	TTACAGGCATGAGCT[G/T]CAATCACACTGAGAA	4703
rs181081859	snp	C/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151530392	CAGGGTCGAGGGCCT[C/G]GATCTGGGCTTTTTC	4703
rs181084740	snp	G/T	0.00318978	0.0398085	intron-variant	NEB, RIF1	GRCh38.p7	2:151510064	GTGATTAACTTCTTT[G/T]AATTTATAACTAAGG	4703
rs181092205	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151622387	TTTAAAAAATGAAAT[A/C]TTTATATTATCACAC	4703
rs181093863	snp	A/G/T	0.000134127	0.00818826	intron-variant	NEB	GRCh38.p7	2:151553790	GTGGGGCCGTGGGGC[A/G/T]GGGCCGTGGAGGGGT	4703
rs181095651	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151649591	AGTAATCTTTCCCTT[A/C]TTTGCATATAATTAC	4703
rs181097573	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151640169	TTTAGTTTGGTGGAC[A/G]GGCCAGGTATCACAC	4703
rs181099406	snp	G/T	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151630021	AAATGGTAGAACAAT[G/T]TTTAATATCTATCTA	4703
rs181115077	snp	C/T	0.00318978	0.0398085	intron-variant	NEB	GRCh38.p7	2:151672742	TTAGCGCTGCAATTA[C/T]ATTCACATATAAAGA	4703
rs181116715	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151691542	CAGCACCAAGGAAAG[G/T]GCCTGGCCCAGCATG	4703
rs181127841	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151733065	ATTCACCTACACAGC[C/T]TTGATTGTCACTACA	4703
rs181131090	snp	A/G	0.00478085	0.0486577	intron-variant	NEB	GRCh38.p7	2:151714454	TTTGCCAGGATCCAA[A/G]TTCATAGTCTTTCTG	4703
rs181150718	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151538577	TGTACAATTTCGGTA[A/C]ATCTAAGACTACTTA	4703
rs181169785	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151570980	AAGCATTTATCATGT[C/T]TGTGTCATAAACATT	4703
rs181179297	snp	C/T	4.19278e-05	0.00457845	intron-variant	NEB	GRCh38.p7	2:151612429	TTTATAGATGTCACC[C/T]AGACGGCCTGGTGCC	4703
rs181232914	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151501104	TAAATAAGAGCTTTA[A/G]TGTTTGGTTTTTCTT	4703
rs181233980	snp	A/C			intron-variant	NEB, RIF1	GRCh38.p7	2:151522129	GCCTATTATGGATGT[A/C]GTATAGGAAAGTGAT	4703
rs181243882	snp	A/G	0.000798403	0.0199641	downstream-variant-500B, intron-variant	NEB, RIF1	GRCh38.p7	2:151484891	GTACGTTGGTCATTC[A/G]CAAGTGAGTGCGCTC	4703
rs181244403	snp	A/G	0.000198985	0.00997261	missense	NEB	GRCh38.p7	2:151678027	AACATATCATGGGGC[A/G]TGTTGTATTTGGACT	4703
rs181246909	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151696254	GGCCAGGGTATGTGC[A/G]GTGCATATTTCTTCC	4703
rs181278542	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151556842	CAGGACTTGAACTCA[A/G]AATCTCTGGGACACA	4703
rs181283540	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151730301	AATGAAGGGGAAAAT[A/G]AGAAGATTCTTCATC	4703
rs181283842	snp	C/T	0.00159617	0.0282053	intron-variant	NEB, RIF1	GRCh38.p7	2:151533821	AGAAAAGAAGACATC[C/T]TTGGAATAGAAAGAT	4703
rs181297079	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151573842	CGTAACTGGATTATC[C/T]TGTACTCACAAATAG	4703
rs181305099	snp	A/G	0.00279162	0.0372561	intron-variant	NEB	GRCh38.p7	2:151618004	GGTGGAGGTTGCAGT[A/G]AGCCAAGATCGTGCC	4703
rs181315930	snp	A/T	0.00478085	0.0486577	intron-variant	NEB	GRCh38.p7	2:151655545	TCAGATTTAAAAAAA[A/T]AATCTTTTAAGTATT	4703
rs181338522	snp	A/G	0.00398564	0.0444627	intron-variant	NEB	GRCh38.p7	2:151720137	CTGATTTTTAAAAAA[A/G]TAAAAAAAAAAAGTT	4703
rs181400452	snp	A/G			intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151506613	GGGAGGGATAACAAA[A/G]GAAATCACAATGTCA	4703
rs181414006	snp	C/T	0.00398564	0.0444627	intron-variant	NEB, RIF1	GRCh38.p7	2:151488464	CCAGCCTGGGCAACA[C/T]AGTGAGCCTCTACCA	4703
rs181443897	snp	C/T	0.0189856	0.0955633	intron-variant	NEB	GRCh38.p7	2:151545431	AAATACAAAATTAGC[C/T]AGGCGTGGTGGCACA	4703
rs181450572	snp	C/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151515872	TTCTTTATAGTTGGA[C/G]GAAGAGAGGCAAATG	4703
rs181454588	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151725282	TTTTAGAAGTTTCTT[C/T]GGGTTCACATTTACA	4703
rs181454739	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151673954	TGAGCCACCATGCCC[A/G]GCCAAAATTTTGTTT	4703
rs181475349	snp	A/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151710629	GATTAACTTTTAAAA[A/T]TATCTTCAGCAAGCC	4703
rs181540796	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151630524	CACCACGAACAGAAA[A/G]GACATTGTGACTTCA	4703
rs181547295	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151683470	GTTGTTTTTTACTCT[A/G]GGCATTTTAAGTAGA	4703
rs181549321	snp	A/C	0.000108089	0.00735069	intron-variant	NEB	GRCh38.p7	2:151650126	AGTGCTATTGAGCAA[A/C]CACTAGGTAGCAGGC	4703
rs181551549	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151704647	TCCGTCACCCCTTTC[C/T]TTGAGTCGGAAAGGT	4703
rs181595134	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151526565	GCCCATTATTATTCC[A/G]TCTTTACAGAGGAGG	4703
rs181596662	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151562881	AATGTCTTTTAGATC[C/T]TTATTTCCCATATAG	4703
rs181598432	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151497885	TGGGATAGGGAATCT[C/G]CACCCTCTAGAGAAG	4703
rs181600483	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151502623	TTAGAGAAAACACAG[C/T]TAAAATTTCACACCA	4703
rs181615359	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	NEB, RIF1	GRCh38.p7	2:151485564	GGCACAGAAATAATA[C/T]TGCAGAAGCTTTTAA	4703
rs181642642	snp	C/T	1.67265e-05	0.00289188	missense	NEB	GRCh38.p7	2:151692325	CAGTAATTCATACTC[C/T]TTGCCTTTGTCTTCT	4703
rs181660714	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151720873	CTTTGTTCTGATGAC[C/T]CTCAAATATTAATTT	4703
rs181686899	snp	A/C	0.00478085	0.0486577	intron-variant	NEB	GRCh38.p7	2:151623320	TTAAGGGAAAAACTA[A/C]AAAGATTTACAGTTC	4703
rs181706694	snp	A/C	0.00676609	0.0577691	intron-variant	NEB	GRCh38.p7	2:151660247	TGTTCAACTTCTCCT[A/C]CGGCCTAGTCCTTCT	4703
rs181731062	snp	A/G	0.00358779	0.0422022	intron-variant	NEB, RIF1	GRCh38.p7	2:151523046	TTCAAAAACAATAAA[A/G]TTTTCAAAATTTCAA	4703
rs181747616	snp	A/G/T			intron-variant	NEB	GRCh38.p7	2:151679331	GTCTACAGAAGTAAC[A/G/T]AAGGAAAAAGGGAGA	4703
rs181751377	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151715586	AGAGATCAGAGCTGG[C/T]TCTCTGTCTCCAATG	4703
rs181757132	snp	A/G	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151696385	TTTGAATGCGGTTTT[A/G]TTTGACTCTAGAACT	4703
rs181761568	snp	G/T	0.00914312	0.0669923	intron-variant	NEB	GRCh38.p7	2:151559419	CTAGAAATACCATTT[G/T]ACCCAGCAATCCCAT	4703
rs181790748	snp	C/G	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151579064	CCAGCCTGGGTGACA[C/G]AGCAAGACTCCATCT	4703
rs181802123	snp	C/T	0.00199481	0.0315187	intron-variant	NEB, RIF1	GRCh38.p7	2:151492626	GCCCAGTGAGACACA[C/T]GACCAATTTTGGAAC	4703
rs181805354	snp	C/T	0.00318978	0.0398085	intron-variant	NEB	GRCh38.p7	2:151641145	ATGTCTGTATATTTA[C/T]ACACACAGAAAAAAA	4703
rs181820849	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151564687	TTACCTCCCTTTTCT[C/T]TATTGGTAGGTGCTC	4703
rs181823465	snp	G/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151527294	GGCCCAGCCAAAGGA[G/T]AATAGGCTCCATGGG	4703
rs181826071	snp	C/T	0.00373388	0.0430465	intron-variant	NEB	GRCh38.p7	2:151546334	TATGCATTGTGATGA[C/T]GTGCACTCACCCAGA	4703
rs181828160	snp	C/T	0.0325976	0.123435	intron-variant	NEB	GRCh38.p7	2:151607235	AAAAACCTAAGATGA[C/T]AACAGAGACTGTTAA	4703
rs181837533	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151644991	TTAGTGTAGGCCACT[A/G]TAACACAATGGGAAG	4703
rs181838705	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151626644	CAGGTTCACACCATT[C/G]TCCTGCCTCAGCCTC	4703
rs181871556	snp	C/T	0.00517822	0.0506191	intron-variant	NEB, RIF1	GRCh38.p7	2:151488589	AAGTCGAGACTGCAG[C/T]GAGCTGTGATCATGC	4703
rs181877781	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151507462	CCTTCATTTAAAGCA[A/G]GCAATAAGCCTCTCC	4703
rs181926631	snp	A/G	0.00318978	0.0398085	intron-variant	NEB	GRCh38.p7	2:151665882	ATGTTTGGGTCTAAT[A/G]CCAACATTTTAAATA	4703
rs181929878	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151636185	TCAGTGAAAATGCCA[A/C]ATTAGATTGATCACA	4703
rs181937401	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151709067	TCTTTAGTGACCATC[A/G]TGCTTTAGAATGCTA	4703
rs181947347	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151732706	ATAGATGATTAGCTA[A/G]TTGAAGCAAAGAATA	4703
rs181965940	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151713515	CATGCTGTGTAACAA[C/T]ATGTCACTGAAAGAT	4703
rs181990605	snp	C/T	0.00597247	0.0543191	intron-variant	NEB	GRCh38.p7	2:151575228	TTCTTAATTAAGAAA[C/T]CTCTTAATTTCTTGC	4703
rs181999166	snp	C/T	0.0310518	0.120672	intron-variant	NEB	GRCh38.p7	2:151540187	TTTGCCTGACTAGTA[C/T]TGTTTGGGCATTTTT	4703
rs182011733	snp	G/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151523610	CTCTGAGCTAAAGTC[G/T]GAAAACCTGTCATAA	4703
rs182011930	snp	A/C/G/T	0.000134565	0.00820173	intron-variant	NEB	GRCh38.p7	2:151629680	AGAGTTAAAGCAAAA[A/C/G/T]GTTTGACATCAACAA	4703
rs182013841	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151559769	CACAGGGAGGGGAAC[A/G]TCACACACTGGGTCC	4703
rs182018789	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151541157	AGCTTCGTTTGTCTG[C/T]GGATAACAGGAAGAT	4703
rs182029307	snp	C/T	0.00394874	0.0442581	missense, intron-variant	NEB	GRCh38.p7	2:151579420	CGGTGCAGGTAATGG[C/T]GATAGTCCACATCAC	4703
rs182030730	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151649367	TTATATAAAACTTCT[A/G]ATATATGATATATGT	4703
rs182036549	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151623508	ATTAAGGATACCGGA[A/C]TAGTATCTGGATTTT	4703
rs182039023	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151690377	AGCAAATTCAAGAAT[C/T]GGAAATATTTGCCTT	4703
rs182079003	snp	C/T	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151731091	TGGCTTCAGAAGAAA[C/T]ATTAAAATAAAATGG	4703
rs182138785	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151647342	CTCGAACTCCTGATC[A/G]CAGGTGATCCACCTG	4703
rs182143534	snp	C/T	0.000843615	0.0205206	missense	NEB	GRCh38.p7	2:151669031	CAAATACTCACATCA[C/T]TCATGTTGAGGGCGT	4703
rs182147520	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151689229	TTTTTTTTTGAGACC[A/G]TGTCTGGCTCCATCA	4703
rs182156589	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151711466	GGTATACCTTTAAGA[A/G]AAGGTGAGTGATGTG	4703
rs182184592	snp	A/G	0.00279162	0.0372561	intron-variant	NEB	GRCh38.p7	2:151684401	TTGATAATGATGAAT[A/G]TGATGATTATGATAA	4703
rs182197107	snp	C/G	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151618550	ACAAAATGGGTTATC[C/G]TAGAGAAACACAAAA	4703
rs182207224	snp	C/T	0.00064585	0.0179585	missense	NEB	GRCh38.p7	2:151725500	TGCGAAGTTCTGGAG[C/T]ATCTGTTGTGCTGGC	4703
rs182211152	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151687345	CTCATGAAATTCTTT[G/T]CCACACTACTACCCT	4703
rs182213882	snp	C/T	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151656516	CCTTTGACTAAAAAT[C/T]GATCTAGTGTCAATA	4703
rs182236248	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151611905	AATGTGTGAGGAAGG[C/G]TAATGCAATTGTGAT	4703
rs182252292	snp	C/T	7.43135e-05	0.00609518	missense	NEB	GRCh38.p7	2:151535741	TATTGATCGGAGAGT[C/T]GGCAACATACTTGAA	4703
rs182262864	snp	C/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151517077	TGGGTCCTGACTGGC[C/G]ATATATTTAATGCAG	4703
rs182266681	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151557958	CTTTGAAAACTGGCA[C/T]AAGACAGGGATGCCC	4703
rs182267940	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151641693	TTAACCCTTCTGTGA[C/T]TGTCATTTATTCTTA	4703
rs182280860	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151618927	GTTACAGAGATATGT[G/T]TGGTATTTCCTTAAT	4703
rs182281052	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151575942	AATCTTTTCACGTAA[A/G]TTACTCAAATTTGAT	4703
rs182283687	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151557198	GATATCACCACCGTT[A/C]CCACAGAAATACAAA	4703
rs182325166	snp	C/T	0.00119737	0.0244387	missense, intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151499372	GAATCCCTTTTCCAA[C/T]GTTTTCTTTATACAA	4703
rs182327414	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151552835	TGCTTGAAACTGCTG[A/G]TTTTCACAGAGGGTT	4703
rs182331609	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151509630	TTTTTTTTTGTTTGT[C/T]TGGTTTTTTGTTTTT	4703
rs182440406	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151706326	GATAAACTCAAATCA[C/T]CACATATTCAATCTC	4703
rs182447631	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151660669	GGCTTTGTGGGCTAA[A/C]CAATTGCTGTCATTA	4703
rs182451592	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151726477	TAAACTTTAGTCTTA[C/T]ATAATCCAATGTTCT	4703
rs182460824	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151705674	GTGGAACCAACCTGA[C/G]GGCCCATCAACCAAC	4703
rs182469020	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151656760	ATTAGAACCCAGATT[C/T]TGTGATGATGCATCA	4703
rs182472638	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151628550	ATATTTACAGAAGTC[C/T]GAATTTTCAGCTGGG	4703
rs182494104	snp	C/T	0.000364764	0.0135	intron-variant	NEB	GRCh38.p7	2:151697300	GCCATTGTATTCATG[C/T]CCTGAGAAAAATGTT	4703
rs182495892	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151569875	ACAATTAAGACCTGT[A/G]TTCATACTACCATTT	4703
rs182498474	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151581666	AATTATAAAGTCATA[A/G]AACATACTTGAATAA	4703
rs182498532	snp	A/G	0.0189856	0.0955633	intron-variant	NEB, RIF1	GRCh38.p7	2:151531570	GATCCACCTGCCTTG[A/G]CTTCCCAAAGTGCTG	4703
rs182513864	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151554877	AATCACATAACGAGC[A/G]GCACATTTCTCAGAA	4703
rs182517061	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151623923	TAAAAAAGATGCAGT[G/T]CTTCAAAGGAGAGAA	4703
rs182521252	snp	C/T	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151641965	CTATCCCTCCTCCCT[C/T]CCCCCATCCTATGAC	4703
rs182526686	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151572613	TGAAGTGGCACGATC[A/T]CAGCTCACTGCAACC	4703
rs182526706	snp	A/C	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151661342	TTGAGCTCCACAAAT[A/C]ATTCAATTCTCTGAA	4703
rs182536776	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151684654	AGAACCACAAGGGTC[A/G]TTTGCTTACATACAT	4703
rs182556846	snp	C/G	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151493599	GAAGCAAAAGTTTAA[C/G]AAAGAAGTAAAATCA	4703
rs182560374	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151529160	AGGCCATGTGTCCTA[C/T]AGAAGCTGGTAAATC	4703
rs182563044	snp	C/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151495952	CTCCACCACCCCACA[C/T]GTACCCGTCCTAAAT	4703
rs182569323	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151567579	GCAAATTCAGCCCCC[C/G]AGCTTTTTGTTTGAC	4703
rs182574133	snp	C/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151511874	TTTCTTCCAGATCTG[C/T]GCACACATTTTTAAA	4703
rs182601770	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151530016	CTCCTTCTGTGCTCC[A/G]GCAGTTATAGCTATT	4703
rs182633534	snp	A/T	0.00183135	0.0302046	intron-variant	NEB	GRCh38.p7	2:151548278	CTATTGAAACTCAAT[A/T]TGTCTCTTGGAGAAT	4703
rs182639010	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151508156	AAACACCACAGGGAT[A/G]TAGGCCAATGGGACC	4703
rs182640047	snp	C/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151528181	TGCATGCTTCCTAGA[C/T]CCTTCAGGGCTGGAG	4703
rs182680682	snp	C/T	0.00478085	0.0486577	intron-variant	NEB	GRCh38.p7	2:151697944	GGTGGCGGGTGCCTG[C/T]AATCCCAGCTACTTG	4703
rs182688045	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151722562	TTGTTTGTTTGTTTT[C/T]AAGATGGAGGTCTCG	4703
rs182699929	snp	A/G	3.31257e-05	0.00406962	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151490023	GTTGTCTGTTGGGTA[A/G]CAACTGAAGATGATC	4703
rs182722471	snp	A/T	0.0185938	0.0946107	intron-variant	NEB	GRCh38.p7	2:151576751	TGCTAGCCAGGCTGG[A/T]CTCAAACCCCTGACC	4703
rs182725059	snp	A/G	0.000770713	0.0196154	synonymous-codon	NEB	GRCh38.p7	2:151675365	GTATTTATGTTTCAC[A/G]TCTTCTCCTTTAGCC	4703
rs182735804	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151637780	ATTATAGGTTTGGCT[A/G]ATAATTCAGTCCTTT	4703
rs182737073	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151609570	TTTTGGATCTAGCAT[A/G]ATAGCAACAATTATT	4703
rs182739836	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151619196	TTCATCTGATTCAAA[C/T]AAAGGAAGCCTGAAT	4703
rs182747961	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151716572	TAGATCCTTTATCCA[A/C]ACAGCTCATAGTTAC	4703
rs182748664	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151680164	TTGCATATTCATGTG[A/C]AAATATCTGTAGGCA	4703
rs182755140	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151681209	TTTGCATGGCACAAA[A/C]AAGTTCTCTTTTTCC	4703
rs182763301	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151722347	GCTGCTGTTGCTGCT[A/G]GTTTCAAGCCTAAGG	4703
rs182818106	snp	G/T	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151632633	GTAATCCGAGATCGC[G/T]CCACTGCACTCCAGC	4703
rs182828710	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151504035	GTTTTCTGAATTGGG[A/G]GAAGTCCATATTTTT	4703
rs182831881	snp	C/T	0.00676609	0.0577691	intron-variant	NEB	GRCh38.p7	2:151550433	ATATGCAAGCCATCA[C/T]GAAGATATAGCCAGG	4703
rs182845454	snp	C/G	0.00318978	0.0398085	intron-variant	NEB, RIF1	GRCh38.p7	2:151524815	GGGGACTGCAGGTGT[C/G]CACCACCATGCCCGG	4703
rs182847302	snp	C/T	0.00675283	0.0577132	synonymous-codon	NEB	GRCh38.p7	2:151553999	GATTTTCATCTTGTT[C/T]TTTTCATAAACTGAT	4703
rs182850862	snp	A/C	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151636803	CAAAACAAAACAAAA[A/C]AAAAAGATACCCATA	4703
rs182860337	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151504603	AAAGAAAATCAAATG[A/G]GAGTTCAGTCCTCCA	4703
rs182860509	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151613103	TCTCTTTTTTTAACT[C/G]TCACTGCTTTTATCA	4703
rs182862081	snp	A/G	0.0260105	0.111035	intron-variant	NEB	GRCh38.p7	2:151571194	ATTTTTAGTAGAGAC[A/G]GGGTTTCTCCATGTT	4703
rs182866658	snp	A/G	0.00114756	0.0239262	missense	NEB	GRCh38.p7	2:151541458	TTACCTGACTCTGAA[A/G]CTTCTGCCCTCGCTT	4703
rs182911246	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151487110	ATATGCTGCTAATTT[C/T]ATTTATGGCCTTTTT	4703
rs182917076	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151530463	AGGCCAAAGTAAACT[A/G]TTCCGAGGGAGCCAT	4703
rs182962645	snp	G/T			upstream-variant-2KB	NEB	GRCh38.p7	2:151734846	AATGTACTCACTCTG[G/T]TAAGGTTCACCAGGT	4703
rs182975692	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151707051	GTTATTTTTGCCCCC[A/G]TCTCTATTATGAATA	4703
rs182983409	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151726861	CAAGACCCTACCTCT[A/G]TGAAAAAATAATTAG	4703
rs183005795	snp	A/T	0.00478085	0.0486577	intron-variant	NEB	GRCh38.p7	2:151652302	GCGATCATGGCTCAC[A/T]AAAGCCTCAGCCTTC	4703
rs183019145	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151693665	TTTATACAATCTATC[A/G]TTGTTGATTCCTTGT	4703
rs183061446	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151645900	CTTATGATGATATGT[A/G]TAACAACGGACTGCA	4703
rs183069769	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151549017	CCCTAAGCCTTCCCC[A/G]TGGGGTAAATGCATC	4703
rs183073860	snp	A/G	0.000399281	0.0141238	synonymous-codon	NEB	GRCh38.p7	2:151560655	GCTGGAAGGCAGGAT[A/G]TAGCTGGTGGCTTTC	4703
rs183078519	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151609247	TTAGACATACAAATC[C/T]TTAGCTGAAAAATAA	4703
rs183081714	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151688064	TAAAACTCCAGGGAA[C/T]AGTAGACGGGTAATT	4703
rs183082792	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151566522	GCATTAGCTTCTCTG[C/G]GCACCTAAGCAACTA	4703
rs183088493	snp	A/T	0.000704367	0.0187533	intron-variant	NEB	GRCh38.p7	2:151616117	TAGAGTTTCTGTAGA[A/T]AAGAAAGTCATTACT	4703
rs183094101	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151628118	CCTATGGCTTGTAGA[A/C]GTTAAGTTTCTGAAA	4703
rs183097140	snp	A/G	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151646568	GTGTTTAATTTAGAG[A/G]CAGCCCTTGCCTTTT	4703
rs183099377	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151668198	TAACAGAAGGTTTTC[A/G]TTTATTTGTCATAAT	4703
rs183123066	snp	C/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151487056	GAAATTGTGTGTGTG[C/T]GCGCATGTGCGTGTG	4703
rs183142350	snp	A/C	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151558135	CAACCGTCTCAGCCC[A/C]AAATCTCCTTAAGCT	4703
rs183147528	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151519964	CAACAGGCATTCAAA[C/T]ATATGATCACTGGCC	4703
rs183148841	snp	G/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151528626	CTCTAGCACTAGTGG[G/T]TACTAATTCGGTTAC	4703
rs183154251	snp	A/G	0.0023933	0.0345097	intron-variant	NEB, RIF1	GRCh38.p7	2:151508457	GTGGCAGTAGTCCTC[A/G]CTGGGCTGGATGAAG	4703
rs183168112	snp	A/G	3.31581e-05	0.00407161	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151524317	CTGCATTACCTGGCT[A/G]CTCAGCTTGGCTGCC	4703
rs183190928	snp	C/T	0.00755907	0.0610114	intron-variant	NEB	GRCh38.p7	2:151698151	AATTATAAGACTGTT[C/T]TGTTAGCAATTATTA	4703
rs183198565	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151722832	GGGATTACAGGGGTG[A/G]GTCACCACATCCAGC	4703
rs183321773	snp	C/G	0.000198682	0.00996502	missense, intron-variant	NEB	GRCh38.p7	2:151627637	GACTAAGGTCTGGCA[C/G]TTCTTGGCTAACACC	4703
rs183333679	snp	C/T	3.33128e-05	0.00408109	missense	NEB	GRCh38.p7	2:151667859	GGGATGGCATCTGGT[C/T]TCAAATCATAGCCCT	4703
rs183338314	snp	A/C	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151663048	ATTCTTGGCTCTATT[A/C]TTTCTCTGTCTTCCT	4703
rs183346372	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151651022	TTGAACTCCCAGGCC[G/T]ACTTTTCTAGCTTCA	4703
rs183349829	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151674753	CATGAGATCATTGGA[C/T]TCTGCACTAATTATT	4703
rs183354017	snp	C/T	0.000248597	0.0111462	missense, intron-variant	NEB	GRCh38.p7	2:151643286	CGTTTATTTTTCTCA[C/T]CCTCGAGAGAACCAC	4703
rs183358017	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151626003	TAACAAATCCTTCCC[A/T]TGATTTTATTTGTTT	4703
rs183359751	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151692607	TTTCAGACTGAAAAA[C/T]GCACACCAATGCTGT	4703
rs183365102	snp	C/T	0.000798403	0.0199641	utr-variant-5-prime	NEB	GRCh38.p7	2:151734449	CCTCTCCCAACTCTC[C/T]CCTCCTGAGAACCCC	4703
rs183368898	snp	C/T	0.000190531	0.00975853	intron-variant	NEB	GRCh38.p7	2:151716153	TTTTCTTTTTTTCTC[C/T]TTTTGAGACAGTTTC	4703
rs183380462	snp	A/T	0.00199481	0.0315187	intron-variant	NEB, RIF1	GRCh38.p7	2:151499724	TAAGTTAGATTAGCA[A/T]GTATTTATTTTCTCT	4703
rs183398468	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151566099	ATCGAGTGCTCAAAT[A/G]CTATTGGAGTTGAGG	4703
rs183417184	snp	A/T	0.00398564	0.0444627	intron-variant	NEB	GRCh38.p7	2:151536229	CACATATTTACTGAT[A/T]GTTTATTCTGCCTCC	4703
rs183418509	snp	G/T	2.49741e-05	0.00353361	missense	NEB	GRCh38.p7	2:151561236	ATGCCACTCTGAACA[G/T]CAGTCACATAGAGGG	4703
rs183425374	snp	C/G/T	2.60834e-05	0.00361124	missense, intron-variant	NEB	GRCh38.p7	2:151625538	AATGATCTTACCTCA[C/G/T]TATAATTTATTTTAT	4703
rs183478564	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151494867	GTTGGTCTTGCTGGT[C/T]TTGAACTGCTGACCT	4703
rs183546398	snp	C/T	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151558613	AGATATATAGACCAA[C/T]GGAACAGAACAGAGG	4703
rs183567111	snp	C/G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151577735	AGGCACATGCCACCA[C/G/T]GCCAGGCTAATTTTT	4703
rs183573045	snp	A/G	0.00318978	0.0398085	intron-variant	NEB	GRCh38.p7	2:151621961	TTACAAAGTTTTGAT[A/G]GGCAATAATGAATTA	4703
rs183575266	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151639590	TGAAATGTATGTTAA[C/T]AAAAGGAAAATGAGA	4703
rs183577481	snp	A/G	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151642233	GTTCATACAGCATAG[A/G]TTGGGTTTTGAAGGA	4703
rs183586235	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151685252	GGAATGATTTTATTC[C/T]AAACCAGGGTTTCTC	4703
rs183602069	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151732948	GTCAATTCTAAATCC[C/T]ACATAATTATAGTGA	4703
rs183605172	snp	A/G	0.00279162	0.0372561	intron-variant	NEB, RIF1	GRCh38.p7	2:151521473	TCTGGACCAAAGGCA[A/G]CTTTTCCTAAGAGAT	4703
rs183605677	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151710914	CAAATGAACTTAGCC[A/G]TTAATTTCTAAGCTT	4703
rs183608868	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151681923	AAAATAGAAACCATC[C/T]ACATATCCCCCAACC	4703
rs183613198	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151537798	AGTTTCTTCAGTTTT[C/T]ATGCCATGTATGATT	4703
rs183619728	snp	A/G	0.00119737	0.0244387	intron-variant	NEB, RIF1	GRCh38.p7	2:151500786	CTATTTTTAGCAGAG[A/G]TGGAATTTCACCATG	4703
rs183631073	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151542499	ATTGCTGCTTCTCCT[A/C]TTTTCTCTATTTTGC	4703
rs183667452	snp	A/G	4.97071e-05	0.00498509	missense	NEB	GRCh38.p7	2:151672622	TTGGGATCATCCTGG[A/G]GGCTTCTGAAACCCA	4703
rs183671974	snp	A/G	0.0146672	0.084371	intron-variant	NEB	GRCh38.p7	2:151601411	CACCATGCCTTGCCT[A/G]AAATAATTTTTAATT	4703
rs183682408	snp	C/T	0.00636936	0.0560724	intron-variant	NEB	GRCh38.p7	2:151714219	AACAATTCCCTCTGA[C/T]CCCTTCCCTGAGTTT	4703
rs183693250	snp	C/T	0.00119737	0.0244387	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151498936	AAATAACAGTAGAGA[C/T]AGAAAAGGTTAGAAT	4703
rs183704293	snp	C/T	0.0221141	0.102801	intron-variant	NEB, RIF1	GRCh38.p7	2:151510849	CCTAAATTTGTGAGT[C/T]AGCTTACATTGCTTG	4703
rs183726277	snp	A/G			intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151534542	TATGACACCAAAATT[A/G]GAGTTCCTTGTGCCC	4703
rs183754353	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151626154	AGTTTCACTCTCTTG[A/C]CCAGGCTGGAATGTA	4703
rs183764569	snp	A/G	0.000317187	0.0125894	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151643821	TCTTAGACTCACATC[A/G]CTCTGGAGGTCATAG	4703
rs183767583	snp	A/C	0.00557542	0.0525036	intron-variant	NEB	GRCh38.p7	2:151617724	AGAGTTATAGCACAC[A/C]GTATTTTTTTTTTTT	4703
rs183768928	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151573789	GATCCATGAAAATGG[C/T]ATCTTCCTTGAACTT	4703
rs183775853	snp	A/G	0.00279162	0.0372561	intron-variant	NEB	GRCh38.p7	2:151664206	AGAGAGGGCCTGGCC[A/G]TGGGCCTCCTGGTAA	4703
rs183789184	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151686371	AACAAATATTTATTA[A/G]GCATTTATTATGTGC	4703
rs183791262	snp	A/G	0.00318978	0.0398085	intron-variant	NEB	GRCh38.p7	2:151730553	TGAACAGAAGGAGAG[A/G]CTCGTTTAGGCCAAG	4703
rs183797539	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151708229	TCTTAAAAAGTCCCT[C/T]TTTACCCAGTTTTTC	4703
rs183801463	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151728537	CTAATAAATGCTTAG[A/G]TGGACAAGAATAATG	4703
rs183819561	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151688480	GCTAAGGCATTAGTG[C/T]TGTTTTTAGAAAAAT	4703
rs183886335	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151686086	AAAACAACAGTTTGT[C/T]TTCGTTAGAAATAAA	4703
rs183912061	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151516742	TGTCTAGGTGTTGAG[A/G]GGATGGGTACCATTA	4703
rs183945135	snp	A/C	0.00119737	0.0244387	intron-variant	NEB, RIF1	GRCh38.p7	2:151491181	TACTACAGGTGTACA[A/C]CACCACTCGCGGCTA	4703
rs183946443	snp	C/T	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151613953	ATAGCACTGTGAGAA[C/T]AGACTAGTACAGAGT	4703
rs183961132	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151728073	TGTAGCCGTATGAAG[G/T]CACATTATGTACACA	4703
rs183994491	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151622554	ATATTTGCTTTCTCT[A/T]GCTCTCTCTTTATGT	4703
rs183998406	snp	C/T	0.00297653	0.038463	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151640541	CTTCTCAAAGTCCTT[C/T]TTGTACTCCCTGTCA	4703
rs184000617	snp	A/C	0.0209421	0.100162	intron-variant	NEB, RIF1	GRCh38.p7	2:151511271	AAAAAGCTAATTATT[A/C]TTCTGCATCCCTACC	4703
rs184001522	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151659651	CAATACAGCAGGGAG[A/G]ATGTAAGATGGAAAG	4703
rs184019514	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151683095	TAACCAAATGTGAGA[C/T]GTTTGTTCCCTGGAA	4703
rs184024704	snp	G/T	0.0448719	0.142907	intron-variant	NEB	GRCh38.p7	2:151702951	TGCAGTTTCTTCCTA[G/T]TCTCGATGGTCTTTA	4703
rs184030064	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151554268	ATGCATTGGTAAATA[C/G]AAAATGTTCAGGCTG	4703
rs184064186	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151707547	GCAGGGAGAAGGAGC[A/C]TTGCTTTTCCTTCTG	4703
rs184116327	snp	A/T	0.0111196	0.0737302	intron-variant	NEB	GRCh38.p7	2:151632164	CACTTTATTAAAAAA[A/T]TTTTTTTTGCTGAAG	4703
rs184153548	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151663348	CTCCCAGCAACAATA[G/T]TAGAAAACAAGACTT	4703
rs184167986	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151702359	TGGTTTGGGGTGGAG[A/G]GCTCTGTAGATGTCA	4703
rs184172192	snp	C/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151495451	CACGTTATTCTGATG[C/T]GTGCTAATGTTTTAG	4703
rs184182602	snp	A/C			intron-variant	NEB, RIF1	GRCh38.p7	2:151531219	AATTCTATGAATTTG[A/C]CAGGTGCTTTCATGC	4703
rs184186637	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151572249	ATCGCTTGAACCCGG[A/G]AGGCAGAAGTTTCAG	4703
rs184228859	snp	A/G	0.00199481	0.0315187	intron-variant	NEB, RIF1	GRCh38.p7	2:151529586	CCCAGGCTGGAGTAC[A/G]ATGGTGTGATCTCAG	4703
rs184235026	snp	A/C	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151568484	ATCATGTTGTCCAAG[A/C]AATTGTTAGCATCCA	4703
rs184246504	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151551191	CCAGGCTGGTCTCGA[A/G]CTCCTGACCTCAGGT	4703
rs184262608	snp	C/T	0.0129278	0.0793521	missense	NEB	GRCh38.p7	2:151659071	TATACTTACATCACT[C/T]ATATTAATTGCATTT	4703
rs184287699	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151492548	AAATCTGAAACCTCA[A/G]AGCCTTTCCAGCAGA	4703
rs184290950	snp	A/G	0.0352966	0.128072	intron-variant	NEB, RIF1	GRCh38.p7	2:151509325	GCTATGTAGATGTAA[A/G]GAAAACAGTTCTCAT	4703
rs184292927	snp	G/T	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151682221	AGAGCTGAAATTTTG[G/T]GGGGAAACTTTTTGG	4703
rs184306056	snp	C/T	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151649391	TATATGTAAAGTGTA[C/T]AGCATATTACATATA	4703
rs184314405	snp	C/T	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151723323	CATCTGGCCAGAATA[C/T]GTAATTCAAGTTCCC	4703
rs184319249	snp	C/G/T	0.00201941	0.031712	missense, synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151492117	AATAGTCTCCTGATC[C/G/T]TGGTCATTCCGTTTT	4703
rs184395708	snp	A/G	0.000399281	0.0141238	synonymous-codon	NEB	GRCh38.p7	2:151717455	CTTGGCAAATTCTAT[A/G]TCTGGAGGATCAGCC	4703
rs184426637	snp	A/G	0.00358779	0.0422022	intron-variant	NEB, RIF1	GRCh38.p7	2:151508871	ACCAGTGGGCAGTCA[A/G]TCTCACCACCAAACT	4703
rs184439256	snp	A/G	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151545510	AACCCAGGAGACAGA[A/G]GTTGCAGTGAGCCGA	4703
rs184448167	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151573233	TTCTTCCAAAATGGA[A/G]GTCATTCTCATTAAT	4703
rs184454057	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151527054	GCAGAAGAAAAGGGA[A/G]GGGTGACAGCACAGG	4703
rs184454256	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151633449	CCCATTTTGTTTTTA[C/T]AAGACCAAGTCCACT	4703
rs184456418	snp	G/T	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151616552	TACAATAATTAACTG[G/T]GCATGGTAGCATGCA	4703
rs184468157	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151719704	GGCAATACGGTGAAA[C/T]CCTGTCTCTACCAAA	4703
rs184471959	snp	A/G	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151652891	TATCTTTAGCACATA[A/G]CACTAAATGGAAATG	4703
rs184479806	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151675821	TTTCCAAATTATAAT[G/T]GTATCAGTGAAAGCA	4703
rs184483437	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151694030	ATACTTATGTATATT[A/G]AGCTCGTTTCTAGGA	4703
rs184516994	snp	A/G	0.000348684	0.0131993	missense, nc-transcript-variant, intron-variant	NEB, RIF1	GRCh38.p7	2:151506941	GATTTTCTTTTACAC[A/G]CAGTATTTCTGGCGT	4703
rs184527760	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151555399	ATTCTCTTGTGGTAA[C/T]GGCTTTGTTTTTCTT	4703
rs184529385	snp	A/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151500299	TGACAATTAAAAATA[A/T]TTTGGATTAATTCCC	4703
rs184533865	snp	A/C	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151488570	AGGATTGCTTGAGTC[A/C]ATGAAGTCGAGACTG	4703
rs184535217	snp	A/G	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151634717	CCTGTAGTAGCAACC[A/G]AGGAGAATTTATTAT	4703
rs184539578	snp	C/T	0.00159617	0.0282053	intron-variant	NEB, RIF1	GRCh38.p7	2:151520838	CACTGCACTCCATCG[C/T]GGGCAACAGAGCAAG	4703
rs184545454	snp	C/T	0.00557542	0.0525036	intron-variant	NEB	GRCh38.p7	2:151676850	TTGTGAATTTCTATA[C/T]CCCATGAATCCTCAT	4703
rs184578813	snp	A/C	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151544692	ATCCTCTGATTCTGG[A/C]TCACTGAGTGTAGGA	4703
rs184586388	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151695019	TCATTACAATACTCA[C/G]TGATGCCAGATAATC	4703
rs184671859	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151654788	GAGTTACCCAGTACT[A/G]TACATCTCAAAAATG	4703
rs184684039	snp	C/T	0.00636936	0.0560724	intron-variant	NEB	GRCh38.p7	2:151611133	TTTTCATCCACTGAA[C/T]CACAAGCTTATTCAG	4703
rs184691199	snp	A/G	0.00478085	0.0486577	intron-variant	NEB	GRCh38.p7	2:151569542	AGGCGGCCAGGCAGT[A/G]TGACAAACGATAGCA	4703
rs184691634	snp	A/G	0.0111196	0.0737302	intron-variant	NEB	GRCh38.p7	2:151629310	CCAATTTTATACTGC[A/G]TTGAAGTATACTGGT	4703
rs184698975	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151488277	AGAAACATTTAAAAT[C/T]TTATGATCAAATTGG	4703
rs184704813	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151648536	CATCCATCACTGGAG[A/C]AACACACATTGTACC	4703
rs184716855	snp	A/G/T			intron-variant	NEB	GRCh38.p7	2:151670959	TGAATTAAGAAGGAC[A/G/T]GAGGAGCGGCTCAGA	4703
rs184718543	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151689841	CAGAAAAGTGGCACA[C/T]GAGCTGAAATGACTT	4703
rs184723737	snp	A/G	0.000688468	0.0185408	missense	NEB	GRCh38.p7	2:151562702	TAGTGTCGATACTCC[A/G]GGTCACTGAGGATGT	4703
rs184753675	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151561667	CAGGTTAGTTACATA[C/T]GTATACATGCCCCTC	4703
rs184759981	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151551934	AGCCTGCTTCCCTTT[G/T]CCTGGAGAACTCATC	4703
rs184760448	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151543714	CTGGCCTCAAACTCC[C/T]GCACTCCAGTGATCC	4703
rs184763330	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151605503	TCAGAAGATAACAAC[A/T]AAAGTTCTGTGGACA	4703
rs184787388	snp	A/C	0.00358779	0.0422022	intron-variant	NEB	GRCh38.p7	2:151689629	GGAGCCAAAGGCAAA[A/C]ATGCACAAGATTGAG	4703
rs184815743	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151525380	TGCTCCCCATTTTGG[C/T]GTCAGTCTGGGACTT	4703
rs184819403	snp	G/T			intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151496805	AGAAGTAGCCCAAAG[G/T]AAAAAAGGATAAATT	4703
rs184830411	snp	C/T	0.00199481	0.0315187	intron-variant	NEB, RIF1	GRCh38.p7	2:151505133	ATATGTATATGCTTT[C/T]AGTTAAATTACTTGA	4703
rs184832657	snp	A/G	0.0205511	0.0992634	intron-variant	NEB, RIF1	GRCh38.p7	2:151522441	TGTTTTCATTTCATC[A/G]TTTAACTTGATCAGT	4703
rs184840355	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151732046	CATCTAAATATAGAC[C/T]GGTCACTAAAATAAT	4703
rs184853095	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151610164	ATCCAGTTTTAAAAC[A/C]ATGCTCATGTGCTGA	4703
rs184870150	snp	G/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151647799	AGACATAGCAAGTAA[G/T]GCAACCTGTGGTCTT	4703
rs184895840	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151670414	TCGCTTCTGACAGAA[A/G]GAATAAGAGTCCATA	4703
rs184910108	snp	C/T	0.00755907	0.0610114	intron-variant	NEB	GRCh38.p7	2:151712052	TTGGAGACAGACCTC[C/T]TCAAGAAACTGAGAA	4703
rs184935875	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151676221	AATAATTTCTTCTAG[A/G]ACCCAAAGAGTTACC	4703
rs184943777	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151694266	CATCCAAGGTTATAT[C/T]AAACAGCAACTTTGT	4703
rs184949560	snp	A/C/G	0.00279162	0.0372561	intron-variant	NEB	GRCh38.p7	2:151719210	TCCTATCCTTGGGAA[A/C/G]CCTTGTGGCCTGCAT	4703
rs184956922	snp	A/G	0.00318978	0.0398085	intron-variant	NEB, RIF1	GRCh38.p7	2:151501894	AATGTTGAAAGCTAA[A/G]TAATACTAGCTTTCA	4703
rs184967272	snp	A/C	0.00119737	0.0244387	upstream-variant-2KB	NEB	GRCh38.p7	2:151736378	GATATTGTCAAGTTG[A/C]CAGTCAAAATCCTTA	4703
rs184967835	snp	A/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151539737	AGCCTTGCCCTCGAT[A/T]GTGTGATATGGAAAA	4703
rs184976275	snp	A/C	0.00438332	0.0466095	intron-variant	NEB	GRCh38.p7	2:151578099	ACTCATTCATTATAA[A/C]AAAGTACCTCTGGAA	4703
rs184980136	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151628666	GCCAACATGGTGCAA[C/T]GCTGTCTCTACTAAA	4703
rs185027498	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151665259	CACTGTAGGAGACGA[C/T]TGGGGCACTGCCAGG	4703
rs185045557	snp	A/G	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151708851	CTTAGACCAAAACCC[A/G]TGTCATCCAATCCAT	4703
rs185065542	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151494474	CTTGAGGACTGCAAG[A/G]GAGACCTGTGGTGTT	4703
rs185089507	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151563375	TGCTTTTTCCTTTTC[C/T]GAACACAAAGCAGTC	4703
rs185101017	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151728943	GCATCTACAGATACT[A/C]GTTTTTATGCAGTCA	4703
rs185113790	snp	A/G	0.00279162	0.0372561	intron-variant	NEB	GRCh38.p7	2:151626598	CTGGAGTGCAGTGGC[A/G]CGATCTCAGCTCACT	4703
rs185128155	snp	A/C	0.00636936	0.0560724	intron-variant	NEB, RIF1	GRCh38.p7	2:151496572	CTAGAGAAGCAGGGA[A/C]CTCAGCTGCTGGGGA	4703
rs185146472	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151687004	ACCAAACTCATTACT[A/G]AAGTCAATGAAGAAC	4703
rs185166179	snp	A/G	0.00480242	0.0487662	intron-variant	NEB	GRCh38.p7	2:151581612	ATGAAAAACGATGGA[A/G]TGGTCAATTAGTAAA	4703
rs185169373	snp	A/G	0.000857077	0.0206834	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151531792	GTTTCTTGCACTTAC[A/G]TCGCTGATTTGTTTG	4703
rs185184424	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151641796	AATGGAAAGATAAAA[A/T]TTTTTAGAAATGTGA	4703
rs185184643	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151623772	GAAACTGGAAGGTCA[A/T]ATACTTTATTTATTA	4703
rs185221488	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151607150	CCCGCCATCTGGATG[C/T]AAATAGAAATGGTCT	4703
rs185226825	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151556578	ATAAAAGGTTTTACA[C/T]AGACTTTAAACCAAC	4703
rs185231134	snp	A/G			missense, intron-variant	NEB	GRCh38.p7	2:151644488	TGGCAATTTCCCGGG[A/G]GGCTTTTGCTGCTTT	4703
rs185253455	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151559912	ACCTCCACGTTCTGC[A/T]CGTGTACCCCAGAAC	4703
rs185257490	snp	A/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151523950	TTTCATTGCTCTTCA[A/T]GTTAAATCTATCCCA	4703
rs185261727	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151541223	CAAAACACAAGTTTT[A/G]TAACACTTAGGAAAG	4703
rs185274755	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151712830	TACAATACATGGAGA[C/T]GGGTTACTCACGTCA	4703
rs185277887	snp	A/G	0.0225045	0.103662	intron-variant	NEB, RIF1	GRCh38.p7	2:151512351	TCTCTTTTTTTTTTA[A/G]GAGTCTCACCCTGTC	4703
rs185293492	snp	A/C	0.00119737	0.0244387	intron-variant	NEB, RIF1	GRCh38.p7	2:151515012	GAAGAAAAAAAAAAC[A/C]GCATTTTCTATGTAT	4703
rs185310037	snp	A/C	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151533097	TATTCAGACCTTTTA[A/C]ATGCTGTTGAATCTA	4703
rs185310275	snp	A/C	0.000798403	0.0199641	intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151497214	GTTGTTGGGATGGGG[A/C]ATCTGCACCCTCTAG	4703
rs185318127	snp	C/T	0.00597247	0.0543191	intron-variant	NEB	GRCh38.p7	2:151638425	GGATTTGAAGGTGAA[C/T]CTGGGGTGAAGGTGG	4703
rs185384768	snp	A/C	0.00279162	0.0372561	intron-variant	NEB	GRCh38.p7	2:151537007	AAGTAAGTATGTACT[A/C]AGACTATAAGGTCTA	4703
rs185394453	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151577198	TGGCTTCCCATCGGT[C/T]ATAGGATAAACATCA	4703
rs185402811	snp	C/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151509529	GGACCTGAACTCCCT[C/G]GTGTTCCCAGACCAA	4703
rs185422916	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151645715	TGCAATGATAATGAC[A/G]ATAAAAATGAGATTC	4703
rs185429034	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151667558	TTTCTTTTTTAGAGA[A/T]GGGATCTCACTCTAT	4703
rs185433570	snp	A/C	0.000666963	0.0182493	intron-variant	NEB	GRCh38.p7	2:151687739	TATAAACATTCTGGA[A/C]AAGAAAAATTCAGCA	4703
rs185441677	snp	C/T	0.000364848	0.0135015	missense	NEB	GRCh38.p7	2:151710459	TTATCAGCATTCATT[C/T]TGGCATTTGCAACTT	4703
rs185453728	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151658386	TTCTTATTGATGCAA[A/G]TAAGAGTTAAAGGAA	4703
rs185468841	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151729988	GATAGAATTTGCTGA[A/G]AAGAGAATACAATAA	4703
rs185473377	snp	C/T	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151571066	GCTGGAGGGCAATGG[C/T]ACCATCTCGGCTCAC	4703
rs185477432	snp	A/G	2.20204e-05	0.00331809	intron-variant	NEB	GRCh38.p7	2:151553792	GGGGCCGTGGGGCGG[A/G]GCCGTGGAGGGGTAC	4703
rs185483510	snp	G/T	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151612842	GCATTAATGTGTTTT[G/T]TTGGGGATAAAAACG	4703
rs185489270	snp	A/G	0.00398564	0.0444627	intron-variant	NEB, RIF1	GRCh38.p7	2:151493521	CACTTAGCTGGTGTT[A/G]TGGCTCATGTTATGG	4703
rs185496567	snp	A/G	0.000165755	0.0091022	missense	NEB	GRCh38.p7	2:151729622	GGCCTTACCTCTCCC[A/G]GCACCTCTTCGTAAA	4703
rs185515742	snp	A/G	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151529773	ACCTCAGGTGATCCC[A/G]CCCACCTCAGCCTTT	4703
rs185521149	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151558372	ACTAAGAGAGGACAC[A/G]AACAAATGGAAAAAC	4703
rs185529193	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151619886	ACTGGTCATGCTGCT[A/G]TAACGCCACATATTG	4703
rs185559101	snp	C/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151494763	AAGTGATTCTTCTGC[C/G]TCAGCCTCCTGAGTA	4703
rs185562450	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151654395	ATCACGTATCTTTCT[C/T]ACTGCTGTTTAATAC	4703
rs185565516	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151530415	GCTTTTTCATTAATC[A/G]TTGGGGAAGGATCCT	4703
rs185571652	snp	C/T	0.00318978	0.0398085	intron-variant	NEB, RIF1	GRCh38.p7	2:151510247	GCCTGGGGAGTTTTT[C/T]TTAGACCCACAGTAA	4703
rs185574478	snp	G/T	0.00221488	0.0332044	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151516486	CTGCTGAGACTCTTT[G/T]GCAGTGATGTACGTT	4703
rs185624242	snp	C/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151513252	GATATTCTAAGCAAG[C/G]AATTCCTGGCATCAA	4703
rs185639566	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151555786	CCAACCAAAATTTCC[A/G]CTAGATTTTTCCAAA	4703
rs185651552	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151617013	AGCAAAATAATATGC[A/G]GCTTACTAACTCATC	4703
rs185656394	snp	A/C/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151641970	CCTCCTCCCTCCCCC[A/C/G]ATCCTATGACAGGCC	4703
rs185672413	snp	C/T	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151661850	AATGTCTATTCAACC[C/T]CACCTTAGACAAACA	4703
rs185674525	snp	A/G	0.000233492	0.0108024	synonymous-codon	NEB	GRCh38.p7	2:151684874	CTTATAATCAACGTC[A/G]CTGGCAATTGCCTGA	4703
rs185683423	snp	C/G	0.00358779	0.0422022	intron-variant	NEB	GRCh38.p7	2:151706339	CATCACATATTCAAT[C/G]TCTCTCTCTCTCTCT	4703
rs185691600	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151726545	CATGCAATCAAGCCA[C/T]CCAGTGAGACCTCAG	4703
rs185692915	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151487632	GGACATTTAGTTGTC[A/G]CCATTTTTTCTTACA	4703
rs185695867	snp	G/T	0.000107126	0.00731788	intron-variant	NEB	GRCh38.p7	2:151634013	TGTAACCCCTTAGAG[G/T]CCACAAGTCTGTGCA	4703
rs185718626	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151566168	GGCTTACCAAGGAGG[C/T]TGTACTTTTAGATGG	4703
rs185724204	snp	C/T	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151635964	AAGCCTGCAGCTTCA[C/T]TCTAACAGGGTCCAC	4703
rs185727779	snp	A/T	3.31411e-05	0.00407056	missense, intron-variant	NEB	GRCh38.p7	2:151618370	GACGCTGACGGTAGA[A/T]AGTATCACTAAGTAA	4703
rs185730143	snp	A/G	3.37781e-05	0.00410949	intron-variant	NEB	GRCh38.p7	2:151548451	TGAGATCAATGATGG[A/G]TAAACAAGGACCAAC	4703
rs185740450	snp	G/T	3.31538e-05	0.00407134	missense	NEB	GRCh38.p7	2:151656259	GTGTTGGTGATGTTG[G/T]CTTGGGCATCCTTTG	4703
rs185744543	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151678275	TGAAGTAATTGAGCT[C/T]CCCAAAAATTACTGT	4703
rs185755655	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151705938	AATGTTGGGGTGGGA[A/G]TGAGGGAGTAAAGAC	4703
rs185756357	snp	G/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151532149	TCACCCAGGCTGGAG[G/T]GCAGTGGTGCGATCT	4703
rs185759242	snp	C/T	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151696256	CCAGGGTATGTGCAG[C/T]GCATATTTCTTCCTT	4703
rs185765592	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151720370	AGGGCTCTGTGCCCA[A/G]TAATTGTAGAAGTTC	4703
rs185766723	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151573493	AGAATGCGCTGCACC[A/G]TGATATTGATATCTG	4703
rs185807088	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151574558	TAAATCTAATAAAAT[G/T]AGCCTTTTCTTCTTG	4703
rs185810149	snp	A/C	0.0111196	0.0737302	intron-variant	NEB	GRCh38.p7	2:151629755	ATAGGAACTGGAGAC[A/C]ATTCAAGTTTCTGGC	4703
rs185862134	snp	C/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151503242	TACACAACACACACA[C/G]ACACACACAGAATTG	4703
rs185876029	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151530027	CTCCGGCAGTTATAG[C/T]TATTATCATATCGTG	4703
rs185895596	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151726359	TAGAAACCTGTCTTA[C/G]ATTATTTAAGGCTCT	4703
rs185967154	snp	C/T	0.00318978	0.0398085	intron-variant	NEB	GRCh38.p7	2:151631013	AAATTATTTAGAGGA[C/T]TTCAAGCATGTAATT	4703
rs185971561	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151613201	ATATTTGAGTCTCCA[A/G]AGGACTCTACTGGCC	4703
rs185977009	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151684583	TTCCCAGAGGGAAAC[A/G]GTGATAGGGTGCAAG	4703
rs185977475	snp	A/G	0.000300125	0.0122463	intron-variant	NEB	GRCh38.p7	2:151650399	GAAAAGACAGAGCAA[A/G]CCATCAAAATCCCAT	4703
rs185986903	snp	A/G	0.00199481	0.0315187	intron-variant	NEB, RIF1	GRCh38.p7	2:151486651	TGGTATATCCATACA[A/G]ATCTATTATTGGGTA	4703
rs185991970	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151725296	TTGGGTTCACATTTA[C/T]AGCAACATGATCTAT	4703
rs185994752	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151674315	AACTGAAAAGAACCA[C/T]AAAAATGTTTCTAAA	4703
rs185999504	snp	C/T	3.31972e-05	0.004074	missense	NEB	GRCh38.p7	2:151553405	AAACTCACATCATCA[C/T]GTAGATCATAAGCAT	4703
rs186001008	snp	C/T	0.00089821	0.0211731	intron-variant	NEB	GRCh38.p7	2:151692378	CTGTTAAAGGAAAAA[C/T]AAATTAAACCAAAAA	4703
rs186003676	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151509859	ATGATCCACCCACCT[C/T]GGTCTCCCAAAGTCC	4703
rs186011254	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151722386	AAGCCTTTTAAGTTC[C/T]TCTAACATACAGTTT	4703
rs186033390	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151612018	ATTAGGGGGCAGGGT[A/G]TTGAGAAGAGCACAC	4703
rs186059084	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151571456	GTTATTGAATTTCTT[C/T]AATGCAATAATTCAA	4703
rs186119200	snp	C/G/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151507951	ATCCAGAGGCATCTT[C/G/T]CTCAGCACCCCTAGG	4703
rs186119279	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151548108	CATAATCTATGGAAC[C/T]GAGTCTCTCCAAGGC	4703
rs186148504	snp	A/C	0.00597247	0.0543191	intron-variant	NEB	GRCh38.p7	2:151608959	AACATTTAATGAAAA[A/C]ATTGGCAAAGATTGT	4703
rs186233985	snp	G/T	0.000266689	0.0115444	synonymous-codon	NEB	GRCh38.p7	2:151697619	TATGCTCTTTGCTTT[G/T]GTCTTTTCATAGTTT	4703
rs186234156	snp	C/G	0.00199481	0.0315187	intron-variant	NEB, RIF1	GRCh38.p7	2:151527956	GGTATTTATTTTCTG[C/G]CAGGCACTTTTCTAA	4703
rs186234545	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151721353	TCAAGGTCCTGCTGC[C/T]GGCATTCTCACAAGT	4703
rs186244044	snp	C/T	0.000658725	0.0181364	synonymous-codon	NEB	GRCh38.p7	2:151540401	TGGCGTATCTGGAAC[C/T]GGAGTGTACTTGTCT	4703
rs186269502	snp	C/T	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151565363	GTGACTTTTAAGACA[C/T]ACCCCCCAAAGATGA	4703
rs186277681	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151733450	GAAATTGAGGTAAGG[A/C]AGTGAGAGAGTTTGG	4703
rs186278440	snp	C/T	1.65875e-05	0.00287984	missense, intron-variant	NEB	GRCh38.p7	2:151627195	CACTGGAGATCAGAT[C/T]TGTAAATGTTCTGGA	4703
rs186299935	snp	C/G	0.00159617	0.0282053	intron-variant	NEB, RIF1	GRCh38.p7	2:151502940	AGGCACAGAGAGTAA[C/G]GAAGGAAGGAAATGG	4703
rs186310554	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151691991	GAGAAAAACCAAAAA[C/T]AGATCATGATTGTTA	4703
rs186312965	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	NEB, RIF1	GRCh38.p7	2:151485600	CTGTTCTGCAACTTA[C/T]TTTAAAACCCAAAGG	4703
rs186335817	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151489834	CTGATATCATTAATA[C/T]GAAACATGTAATAAA	4703
rs186381848	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151624220	TACATTAATATATTG[C/T]ACTGTGGTGAAGTCA	4703
rs186387814	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151649819	TTTATAACACATCCA[C/T]TGTGCCTGTGTAAGG	4703
rs186405260	snp	A/G	0.00398564	0.0444627	downstream-variant-500B, intron-variant	NEB, RIF1	GRCh38.p7	2:151485304	GTAGATATTAAAACC[A/G]TTAAACATAAATAAT	4703
rs186440374	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151607242	TAAGATGATAACAGA[A/G]ACTGTTAAGAGTGAA	4703
rs186446594	snp	C/T	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151564797	TGAAGGCTTGTCTCA[C/T]TGAGCTTTAGCCCCT	4703
rs186455653	snp	A/T	0.0154538	0.0865337	intron-variant	NEB	GRCh38.p7	2:151626720	TTTTTGTATTTTTAG[A/T]AGAGACAGGGTTTCA	4703
rs186460427	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151645054	CATGGAAAAGATACC[A/G]CAAAAATACAGTATG	4703
rs186460644	snp	A/G	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151665980	ACTCTGAGTTCTGGA[A/G]GGAATCCTTAATTAC	4703
rs186469843	snp	C/T	0.00835141	0.0640778	intron-variant	NEB	GRCh38.p7	2:151626037	GCTGTTTGTTGTTAG[C/T]TTATTAGCTGCAAAT	4703
rs186473611	snp	C/G	0.00504883	0.0499892	intron-variant	NEB	GRCh38.p7	2:151687606	CTGTCCAGGTCCCCA[C/G]GTCCCCAGGCCACAC	4703
rs186474264	snp	A/G	0.00478085	0.0486577	intron-variant	NEB	GRCh38.p7	2:151643611	TGATTGTCTAGCTCG[A/G]CAATCTAGAGGCTTC	4703
rs186475936	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151663446	TATGTTGGGAAATTG[C/T]AGATGAATTTCTTTC	4703
rs186479631	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151716408	TCCCAAAGTGCTGGG[A/T]TTACAGGTGTGAGCC	4703
rs186482561	snp	A/G	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151686090	CAACAGTTTGTCTTC[A/G]TTAGAAATAAACTGA	4703
rs186496961	snp	A/G	0.00398564	0.0444627	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151499032	ATTTGCCAAAGCAGT[A/G]TAAATGTGGATGCTT	4703
rs186498267	snp	C/T	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151714758	TTATACTTTAAGTTC[C/T]AGGGTAGATAAAGGA	4703
rs186504584	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151516880	ATTACCCAGGTAGAT[A/G]AGGTTGGTCAATAAT	4703
rs186511119	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151527337	CTGAGCTCGCCTATC[A/G]CTCCCCCAACCATCC	4703
rs186513448	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151547108	GAGAGGAAAATACTC[A/C]ACATGACCTGGGATG	4703
rs186545304	snp	A/G	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151710857	TCATCCTCTATTTAT[A/G]TTTCAGTTACAATAC	4703
rs186546249	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	NEB	GRCh38.p7	2:151734708	TTGAATTTCCCATTT[A/T]CTGAGGCCCCATTCA	4703
rs186554497	snp	A/C	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151562279	ATTGAGCATTTGATA[A/C]TTTCCTATCAGCTGT	4703
rs186558962	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151544018	TTAACCCTCCCCCGC[C/T]CTCCATGGTTTTTAT	4703
rs186562370	snp	A/G	0.0894459	0.191631	intron-variant	NEB	GRCh38.p7	2:151605516	ACAAAAGTTCTGTGG[A/G]CAAGAGTTTCCATCT	4703
rs186594907	snp	A/G	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151630032	CAATGTTTAATATCT[A/G]TCTATACGTATAAAA	4703
rs186602389	snp	C/G	0.00279162	0.0372561	intron-variant	NEB	GRCh38.p7	2:151673667	AACCAAGATTTTATT[C/G]CCTGGGATAGCATGT	4703
rs186634689	snp	A/G	8.28082e-05	0.00643407	missense, intron-variant	NEB	GRCh38.p7	2:151627791	ATGTTCCGGGCTCCA[A/G]TGTGGTGGCCGAGCT	4703
rs186645591	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151668046	TGAAGTTAGGACTAT[C/T]AGTTTGTCTTTTATG	4703
rs186670134	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151731226	ATCTTAGAAATACGC[G/T]TATAAAAGAGGCAAC	4703
rs186676110	snp	A/G	0.0001831	0.00956642	intron-variant, missense, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151498228	TAATTCTGAAGTTAA[A/G]TGGCATTTTTTCCCC	4703
rs186686151	snp	A/G	0.00023213	0.0107708	missense, intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151534292	GGTATTTATCTTTCC[A/G]CTGCTCATAATCAGC	4703
rs186711305	snp	C/T	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151689353	GAGACTACAGGCATG[C/T]GCCACCATACCCAGC	4703
rs186715931	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151711483	AGGTGAGTGATGTGC[A/T]GAGTCAACGAGCTTG	4703
rs186731051	snp	A/G	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151511615	GAACTCATTGATCAG[A/G]AGACAAGCACAAATT	4703
rs186742391	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151495479	TAGAAGCACTGTACT[C/T]AAGTACTGGAGAAAC	4703
rs186773334	snp	A/G	0.00358779	0.0422022	intron-variant	NEB	GRCh38.p7	2:151688146	AGTAGGAGTCTTAAG[A/G]GCATTTTGGCCTTAA	4703
rs186846560	snp	C/T	0.00716266	0.059414	intron-variant	NEB	GRCh38.p7	2:151609154	GAGTGCAATTGGAGA[C/T]TGCACTCCAGCCTGG	4703
rs186849982	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151730325	CTTCATCACAAAGTG[C/T]GGGAAAGGTAGGCTG	4703
rs186852328	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151646079	ATTTCACTGATTTAG[A/G]AACAATTAAAATGAG	4703
rs186873048	snp	A/G	0.00279162	0.0372561	intron-variant	NEB, RIF1	GRCh38.p7	2:151515891	GAGAGGCAAATGGAA[A/G]TTCCAAATAAGCCCA	4703
rs186881590	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151684134	GAAAAGGCTCTGCAG[A/G]TTGGTTGTACAACAA	4703
rs186889110	snp	C/T	0.00716266	0.059414	intron-variant	NEB	GRCh38.p7	2:151557073	AAAAAATCAATGAAT[C/T]CAGGAGCTGTTTTTT	4703
rs186902443	snp	A/G	0.000645904	0.0179593	synonymous-codon	NEB	GRCh38.p7	2:151576271	AAAGATATTCTGGGC[A/G]TTTTTGACTCTCAAC	4703
rs186909172	snp	A/G	0.00318978	0.0398085	intron-variant	NEB	GRCh38.p7	2:151618985	ACATGCTGAATGTTG[A/G]TAAGTATTAGACGAC	4703
rs186910779	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151637354	ACTGTGGAGGGGAAG[C/T]GGAGGGGTGTTGAAG	4703
rs186931807	snp	C/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151510917	ACAGATTCTCCATTG[C/G]AAATCGAGAAGCAAG	4703
rs186945674	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151499547	CAGATCTGGGTGAGA[A/G]CATGTTTTGTATTTC	4703
rs186959351	snp	C/T	0.000414817	0.0143957	intron-variant	NEB	GRCh38.p7	2:151554056	CACATGCCAGTTATA[C/T]AGGAAATTGTGCCAA	4703
rs186959666	snp	A/G	0.0189856	0.0955633	intron-variant	NEB	GRCh38.p7	2:151535883	TATGATATAATTGTG[A/G]TAATTAATTCATAGA	4703
rs186961229	snp	A/T	0.331179	0.236453	intron-variant	NEB	GRCh38.p7	2:151579196	CTTTCTGAAGAAACC[A/T]GGCTGTAGGTAGGCA	4703
rs186974080	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151519152	AGTGAGATAGCCCAT[C/T]GTCAAACAAATGCTG	4703
rs186976447	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151558047	GAGAAAGAAATAAAC[A/G]GTATTCAATTAGGAA	4703
rs186981408	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151641438	TTGGGCTGAAGTGAT[C/G]CTCCCACCTCAGCTT	4703
rs186981499	snp	A/C	1.65663e-05	0.002878	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151492123	CTCCTGATCTTGGTC[A/C]TTCCGTTTTTGTTCC	4703
rs186982529	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151728776	ATCATCTGTACCAAA[G/T]AATTCTAGCATCAAT	4703
rs187015560	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151733932	CAGAGAGTAAGACTC[C/T]TGATATGAAGTGGAT	4703
rs187074927	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151660249	TTCAACTTCTCCTCC[A/G]GCCTAGTCCTTCTTC	4703
rs187093710	snp	C/T	0.00318978	0.0398085	intron-variant	NEB	GRCh38.p7	2:151704783	CTAGTGAGATGAACC[C/T]GGTACCTCAGATGGA	4703
rs187118760	snp	C/T	2.71492e-05	0.00368427	intron-variant	NEB	GRCh38.p7	2:151616125	CTGTAGAAAAGAAAG[C/T]CATTACTCATTTACT	4703
rs187121305	snp	A/C/G	0.00478085	0.0486577	intron-variant	NEB	GRCh38.p7	2:151572820	CTCCCAAAGTGCTGG[A/C/G]ATTACAGGCATGAGC	4703
rs187125274	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151632660	CAGCCTGGGCGACAG[A/T]GGGAGACTCTGTCTC	4703
rs187133171	snp	A/G	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151530480	TCCGAGGGAGCCATA[A/G]TGGGGTTTACTAAAC	4703
rs187147644	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151559577	CTGGATAAAGAAAAT[A/G]TGGCATATATACACC	4703
rs187148552	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151656527	AAATCGATCTAGTGT[A/C]AATATGCTATATTAT	4703
rs187152462	snp	C/T	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151623393	CTTTTCATTGCTGAG[C/T]CTGTGTAAAGACAAA	4703
rs187156487	snp	C/G	0.000275283	0.0117288	intron-variant	NEB	GRCh38.p7	2:151696622	TGGGTGTCCTGAGTA[C/G]TTAGAGGAACTTACG	4703
rs187180051	snp	A/G	0.00119737	0.0244387	intron-variant	NEB, RIF1	GRCh38.p7	2:151495998	AACAAAGAGACCTTG[A/G]GGGTAGTGGATAGAG	4703
rs187197381	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151531666	CATAACAGGACATCT[C/T]GCACCCCTGCCTCCC	4703
rs187197725	snp	A/C	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151557500	AGAAAAAGAGAGAAT[A/C]CTCCCTAACTCATTT	4703
rs187205809	snp	A/G	0.00358779	0.0422022	intron-variant	NEB, RIF1	GRCh38.p7	2:151512192	CCTGCCACCACGCCC[A/G]GCTAATTTTTGTGTA	4703
rs187208933	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151618829	TGAGACTGATGGTGC[A/G]TGAGTACTGCAGTCA	4703
rs187211085	snp	A/G	0.00107652	0.0231755	synonymous-codon	NEB	GRCh38.p7	2:151554982	TGTGTTCGGATCATC[A/G]TCAACACTTCTTGGT	4703
rs187231245	snp	A/G	0.00676609	0.0577691	intron-variant	NEB, RIF1	GRCh38.p7	2:151488754	TTGAGATGGGTATCT[A/G]ATTTTATTATTTTAC	4703
rs187316268	snp	A/C	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151490351	GGTGGGACTGCCAAA[A/C]TCAGCGCCAGGCACT	4703
rs187319470	snp	A/G	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151528281	AGCCTGCACTATTAG[A/G]CACATTTCTTTCCTC	4703
rs187320768	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151508224	GGGAAAGTCCTTTGT[A/G]TTTTCTTAACTGTCC	4703
rs187343008	snp	C/T	0.0130163	0.079616	missense	NEB	GRCh38.p7	2:151679785	TCAGTTCTCAGGTCA[C/T]ATCCCTTCTTGCTCA	4703
rs187350875	snp	A/C	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151638392	TCATGTGAGGAATGC[A/C]CCGCAGCTTGGGATA	4703
rs187353548	snp	A/G	0.00279162	0.0372561	intron-variant	NEB	GRCh38.p7	2:151658206	TGAGCAGAATGCTTC[A/G]TTGGTGCTTCAGTGG	4703
rs187373194	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151681598	GAGCAGACAAAATGG[C/T]TTTCATCGAAAACAA	4703
rs187375777	snp	G/T	0.00716266	0.059414	intron-variant	NEB	GRCh38.p7	2:151697991	GAATTGCTTGAACCC[G/T]GGAGGCGGAGGTTGC	4703
rs187382304	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151722571	TGTTTTTAAGATGGA[A/G]GTCTCGCTGTTGCCC	4703
rs187390101	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151534766	TATAAAGGAGACCTG[A/G]AAATTCTTCATGAAA	4703
rs187409832	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151575389	CTATCTGAGTCTATC[A/G]TTAATTCTCTTTTCT	4703
rs187429991	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151636198	CACATTAGATTGATC[A/T]CATACTCAGAATGGA	4703
rs187430466	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151619278	TCTCCTACAGAGAAC[G/T]TTTGGAGAAGAAAAC	4703
rs187439208	snp	G/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151674977	AAAAGGGAGCTCATT[G/T]ATTCTTATGTTTCTG	4703
rs187464016	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151707727	TGATCCCCAGTGTAA[G/T]CCCTTTATTCAGGCA	4703
rs187465186	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151507543	GATACTAGGAGAATC[C/T]GAACAAACAGCCATC	4703
rs187468091	snp	A/G	0.00478085	0.0486577	intron-variant	NEB	GRCh38.p7	2:151561449	GGCTGTCATTCTAGA[A/G]TCCTGCAGACTTTGT	4703
rs187482922	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151531402	GTTCACTGCAACCTC[C/T]ATCTCCTGGGCTCAA	4703
rs187490587	snp	A/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151572418	TTTGTTTTCATTCTA[A/T]TTTATTATGCACATT	4703
rs187496580	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151505270	GGTAGGAAAAGAAAG[C/T]CAAATCCCTTCTACT	4703
rs187511621	snp	A/C	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151487143	ACCTTTCGAAGAGGT[A/C]AGTCTTGTATTTTAG	4703
rs187522094	snp	A/C/T			upstream-variant-2KB	NEB	GRCh38.p7	2:151735950	AAAAAATAATACAGG[A/C/T]CCATACTTTAAAAAC	4703
rs187522643	snp	G/T	0.00557542	0.0525036	intron-variant	NEB, RIF1	GRCh38.p7	2:151525108	AAGAGAATGCACCAA[G/T]CTGGGTTCCACTGCT	4703
rs187530287	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151543016	GCCTTGAATGTTCTT[A/C]TCCCTTTTATTTGCC	4703
rs187535260	snp	A/G	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151504896	GTATAATATACCATT[A/G]TAGGTAGATCGCAGC	4703
rs187560403	snp	C/T	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151653134	ACTCTGTACTTCAAC[C/T]TGCCTATTAACCAAA	4703
rs187573055	snp	C/T	0.00676609	0.0577691	intron-variant	NEB	GRCh38.p7	2:151675885	TACATGAATCTAGCA[C/T]ACTCAAAAGGCTCAC	4703
rs187583991	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151694114	AGGGCATTAAGGAGA[C/T]TAAGGAAAATTTGCA	4703
rs187589358	snp	C/T	0.00716266	0.059414	intron-variant	NEB	GRCh38.p7	2:151718002	GGGACTACAGGCACC[C/T]GCCACCGTGCCCGGC	4703
rs187637065	snp	C/T	0.00054638	0.0165194	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151633714	CTGGTCAGGCAGGCA[C/T]GTCCACTCGTGCAGG	4703
rs187638701	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151616604	GAGGCTGAGGCAGGA[A/G]AATTGCTTGAACCCA	4703
rs187681782	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151550502	CAGTGTGTTGACATC[A/G]GGCCGTGAAGAGGTC	4703
rs187712971	snp	G/T	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151609613	AGATGATTTATATTT[G/T]TCTGAAATATGTTTT	4703
rs187716982	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151628119	CTATGGCTTGTAGAC[A/G]TTAAGTTTCTGAAAA	4703
rs187718056	snp	A/T	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151680531	CAAATGGCTAAAAGG[A/T]CAGTCAGCACAATAT	4703
rs187721334	snp	A/G	0.0111196	0.0737302	intron-variant	NEB	GRCh38.p7	2:151647362	TGATCCACCTGCCTC[A/G]GCCTCCCAAAGTGCT	4703
rs187729385	snp	C/G	0.0193772	0.0965046	intron-variant	NEB	GRCh38.p7	2:151646886	AACTCCCCACCTCAG[C/G]CTCCCAAAGTGCTGG	4703
rs187734567	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151668307	CTTATAGGAAGATAT[A/G]AATACTAAAACTAAA	4703
rs187735737	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151525615	CAGAGATTACTGAGG[C/T]CCAAAGAGGTAGTTT	4703
rs187739126	snp	A/G	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151487740	TCAAATGGCATGTGT[A/G]TTTAAACTTATTTTA	4703
rs187744672	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151688530	TTCAGTCAAAGTCTC[A/G]CACAGGATTCAAACT	4703
rs187747572	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151554677	AATGTTTCAGTCAAA[A/G]GATTATAATGCTGAG	4703
rs187757470	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151615408	CCTTAGGAGGTGTTT[C/T]GCATGTGAAGAAAAG	4703
rs187764127	snp	A/G	0.00119737	0.0244387	intron-variant	NEB, RIF1	GRCh38.p7	2:151509014	TCCCACTCTTCAGGG[A/G]AGTTTTAGTTTGTAG	4703
rs187764790	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151651073	TTACAGGTACATGCC[A/T]CCTCATCCAGCTTCA	4703
rs187781350	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151520928	AGTGACAGAAACATC[C/T]CCTAATTGAAAAACA	4703
rs187787674	snp	A/G	0.00318978	0.0398085	intron-variant	NEB	GRCh38.p7	2:151550227	AGCTGTGATTGCACC[A/G]TTGCACTCCAGCCTG	4703
rs187796360	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151609279	GCACATGGGGTTGAC[A/G]GGATAAGTGCACGAG	4703
rs187798139	snp	A/G	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151537328	ACAAACAGAAGCACT[A/G]CCCCTTGAGGTATAT	4703
rs187804983	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151566605	GAGATCTTGATTCAG[G/T]CTTCAGTGGGAGGTA	4703
rs187960545	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151652321	GCCTCAGCCTTCCAA[A/G]CTCAAGTGATCCTCC	4703
rs187967107	snp	A/G	0.0023933	0.0345097	upstream-variant-2KB	NEB	GRCh38.p7	2:151735144	GAACCTCTCTCATAT[A/G]TAACCGAGTTAGTGA	4703
rs187974537	snp	C/T	0.00716266	0.059414	intron-variant	NEB	GRCh38.p7	2:151693864	TCTTAAAATAAAATG[C/T]TTTGCTTTTGAGTTT	4703
rs187977960	snp	A/G/T	0.000447427	0.0149505	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151529272	CATCTGGCTCAATGG[A/G/T]GCAGTTGGATTTATT	4703
rs187984065	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151567952	ATCACCAAGCCTGGC[C/G]AGGTCTGCCACACTG	4703
rs187993459	snp	A/G	0.00358779	0.0422022	intron-variant	NEB	GRCh38.p7	2:151657116	GCCTGTCTCCTTTTG[A/G]GGTTGCGTGTGCAAG	4703
rs187997329	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151628620	CCGAGGGAGGCGGAT[C/T]GCCTGAGGTCAGGAG	4703
rs188004000	snp	A/G	1.65641e-05	0.00287781	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151524587	TGTGGTGTAATGCAG[A/G]TTCTCTTTGGCATCT	4703
rs188017153	snp	A/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151560793	GTCTGTCCTTCTCAC[A/T]CACTCCCTACTAACT	4703
rs188042437	snp	A/C	0.021333	0.101051	intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151497126	GCTTCCTTGTTAAGA[A/C]AAAACACAGTTGTCC	4703
rs188046646	snp	A/G	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151532363	TGTTTTACTCATAAC[A/G]TATTGTATTGAACAT	4703
rs188057733	snp	C/T	0.00159617	0.0282053	intron-variant	NEB, RIF1	GRCh38.p7	2:151487058	AATTGTGTGTGTGTG[C/T]GCATGTGCGTGTGTG	4703
rs188127282	snp	C/G	6.62712e-05	0.00575597	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151627014	CACCTTGTTCATATT[C/G]AGAGCATTGTTCTTG	4703
rs188131010	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151712384	TGAGCAGGAGATTAA[A/T]TCTCACAGTGAGAGA	4703
rs188169532	snp	G/T	0.00279162	0.0372561	intron-variant	NEB	GRCh38.p7	2:151716799	AGCAGCAGTATCCCA[G/T]GAGAAAGTGGTCTGA	4703
rs188208355	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151670484	AATGAGACATACAGA[C/T]GTGGTATGAGTCCAC	4703
rs188212054	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151639740	AAGCCAATAGATACA[C/T]AGACAGATAGATAGA	4703
rs188212129	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151621981	ATAATGAATTAAGTT[C/G]TCTGGTAGAGTTTTG	4703
rs188224691	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151659486	TTGTATTTTTTGTAG[A/G]GATGGGTTTTTGCCA	4703
rs188234435	snp	A/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151682477	TGTAAGGAATGGTTA[A/T]CATAAATGATTTTGG	4703
rs188247438	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151675592	AATAGAAGGAGAAAA[A/C]ATCCTTAAGAAAATA	4703
rs188248744	snp	A/G	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151536571	CATGAATTAGAATGG[A/G]TTTCACCATTCCACA	4703
rs188253334	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151577016	TCTCCATTTGAGGGA[C/T]TGCATGGAAGACTTC	4703
rs188256987	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151521709	CAATCCCATTGATTC[C/T]ACTTCAGTTTCTTTT	4703
rs188261363	snp	G/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151494558	GCCCCTGAGAGATGA[G/T]CCAAACAGGAGTTAC	4703
rs188276627	snp	C/T	0.00398564	0.0444627	intron-variant	NEB	GRCh38.p7	2:151558748	AACTGGCTAGCCATA[C/T]GCAGAAAGCTGAAAC	4703
rs188278168	snp	G/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151504174	GAGTTCTTTTAAATG[G/T]ATGGATTCCCTGGTG	4703
rs188280277	snp	G/T	3.33456e-05	0.0040831	synonymous-codon	NEB	GRCh38.p7	2:151541474	CTTCTGCCCTCGCTT[G/T]GCTCTTAAAAGATCA	4703
rs188287498	snp	A/T	0.000826887	0.0203165	intron-variant	NEB	GRCh38.p7	2:151538008	AAAGACAGCTGTAAG[A/T]CTTACCCAAAGTTAA	4703
rs188291055	snp	A/T	0.00914312	0.0669923	intron-variant	NEB	GRCh38.p7	2:151581723	AATTTTATAATAAAT[A/T]AAAACTAACATAAGT	4703
rs188291311	snp	A/G	0.00279162	0.0372561	intron-variant	NEB	GRCh38.p7	2:151577871	GGTGTGAGCCACAGC[A/G]CCCAGCCTATGTCAT	4703
rs188298019	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151714288	TGTCAGAAACCTGGA[C/G]AGACTACTGTCATAA	4703
rs188298520	snp	C/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151509945	GGTTACCGGGAGAAG[C/G]CCTGGAAATTATCAC	4703
rs188311818	snp	C/T	0.00119737	0.0244387	intron-variant	NEB, RIF1	GRCh38.p7	2:151499811	TATGGCAATTTGGTC[C/T]TTGTCATTAAGTTCA	4703
rs188363427	snp	A/G	0.00517822	0.0506191	intron-variant	NEB	GRCh38.p7	2:151733023	CTTTGTGAAGTTATA[A/G]TAGACAATGTATTTT	4703
rs188402822	snp	G/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151732408	CTTTGTAAAATGTGT[G/T]AGATGTCCACTAATA	4703
rs188425912	snp	A/C/G	0.00319074	0.0398324	intron-variant	NEB	GRCh38.p7	2:151685489	ATTGACAGGAGATAA[A/C/G]CCCACTGAGAATCTC	4703
rs188444022	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151727447	CCAATAAATGCTTTA[G/T]GATTGGCCTTATGCT	4703
rs188454298	snp	C/T	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151664682	TGACTACAAAGTGGT[C/T]GGTATGTAGAATGCA	4703
rs188456299	snp	C/T	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151617928	TGCTGGGTGTGGTGG[C/T]AGGCTCCTGTAATCC	4703
rs188458344	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151635057	TCAGAGTCCCAACTC[A/C]CCCACTCACTAGGAG	4703
rs188458494	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151686450	CATGCTATCAATGGG[A/G]AGTTATATCCTTCTT	4703
rs188460616	snp	C/T	2.26308e-05	0.00336376	intron-variant	NEB	GRCh38.p7	2:151655409	GACATGAAATTTGAA[C/T]AACTGGGACAAGCAG	4703
rs188466758	snp	C/G	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151708488	GCATTGCCCTCTCCT[C/G]ATTTTGCTTCTCCCT	4703
rs188498310	snp	A/G	0.0023933	0.0345097	intron-variant	NEB, RIF1	GRCh38.p7	2:151515528	TTGACCTGTTTTTTA[A/G]AAATCACTGAATAGC	4703
rs188499923	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151605320	GAAAACAAGGCACAG[A/G]TGATAATCTCCATCA	4703
rs188503474	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151689793	TGTTAGTGTTTAGCT[C/G]TTCTTTATTGGGACA	4703
rs188510244	snp	A/G	0.00318978	0.0398085	intron-variant	NEB	GRCh38.p7	2:151642480	GTTAGCAACAGCTTT[A/G]ACCTCATGGCTTACT	4703
rs188510472	snp	G/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151533670	TTATGTACTCACATA[G/T]GTGCGGGTGAAGACA	4703
rs188524908	snp	C/T	0.00557542	0.0525036	intron-variant	NEB	GRCh38.p7	2:151556768	AATAATAGTGGGAGA[C/T]TTTAACACCTCCTGT	4703
rs188534403	snp	A/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151520272	TATCATTTAAAAATT[A/T]TTAAACTTGGCCAAA	4703
rs188545440	snp	C/T	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151573802	GGTATCTTCCTTGAA[C/T]TTTCTTGAATTGTGT	4703
rs188548723	snp	C/G	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151558289	AAGATAATAAAATAC[C/G]TAGGAATCCAACTTA	4703
rs188685325	snp	A/T	0.00557542	0.0525036	intron-variant	NEB	GRCh38.p7	2:151698204	CCAAACTCAAAAAAA[A/T]TTTTTTTCTTTCTTT	4703
rs188700206	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151683334	TTTGCATAAGAGGGC[A/G]GTTATTATTTGGAAT	4703
rs188718613	snp	C/T	0.003291	0.040431	missense	NEB	GRCh38.p7	2:151724895	TCTTTGCATGTTCAA[C/T]ATCCTTTGCTTTTTC	4703
rs188719625	snp	C/T	0.00755907	0.0610114	intron-variant	NEB	GRCh38.p7	2:151707387	AGAACCTTCACTCAG[C/T]TCTCAACCCCCAGCT	4703
rs188721359	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151488407	ATCCCAGCATTTTAG[A/G]AGGCCAAAGCAGGCA	4703
rs188734420	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151558465	CTATAGATTCAATGC[C/T]ATCCCCATCAAGCTA	4703
rs188740682	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151620465	GATTAATTTTTAAGA[C/T]GTCCAGGGATCTGAT	4703
rs188766723	snp	C/T	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151658912	GTCCTACTCCAACTC[C/T]GCAAAGCAAAATTAG	4703
rs188772913	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151730706	AGCACTCAAGGGAAG[A/G]GAAAACATTAAGATG	4703
rs188788701	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151660062	CAAATAGTCTCCAGT[C/T]ACCAGCTGTCTCACT	4703
rs188790192	snp	C/G	0.0193772	0.0965046	intron-variant	NEB, RIF1	GRCh38.p7	2:151528775	CAGGGAATATCTGAG[C/G]AGGAAGAAGGTCTAG	4703
rs188792150	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151491387	TTGCCTATGTATTTT[A/G]TGTATTTTCATTATT	4703
rs188797999	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151663214	TCTTACTTTCCCTTT[C/T]ATTCCTCTATTAAAA	4703
rs188873569	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151610195	CAATTACAGACAACA[G/T]GAAATGGACAAGATT	4703
rs188926325	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151492604	GACGCTTGGGTCAAC[C/T]GAAGGGGCCCAGTGA	4703
rs188932786	snp	C/T	0.00318978	0.0398085	intron-variant	NEB, RIF1	GRCh38.p7	2:151509367	AAGAATAGAAACAAT[C/T]GTCCTTTTATTTTAT	4703
rs188954469	snp	C/T	0.0310518	0.120672	intron-variant	NEB, RIF1	GRCh38.p7	2:151529655	CCTGCCTCAGCCTCC[C/T]GAGTACCTGGGACCA	4703
rs188962186	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151720802	TCCTCCAAAACTCTG[C/T]CCTTGGCCATGCACT	4703
rs188962960	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151568950	TAGCTCTCAAAGTTA[C/T]ATAATGTATCATTAT	4703
rs188969310	snp	A/G	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151551207	CTCCTGACCTCAGGT[A/G]ATCTGCCCGCCTCAG	4703
rs188970233	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151722949	TAGTAAGGCACAACC[C/T]TTCCATAACATTGTT	4703
rs188977183	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151573601	GCTCATTATACCAGA[A/G]CTTATAGAGCTGTTT	4703
rs189009035	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151634658	AAAATAAAATAAAAT[A/C]AAATAAAAACAGTAA	4703
rs189023361	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151676576	TCAGGTTACAATCCT[A/G]AACCTTTTGCTTTTA	4703
rs189026131	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151577553	GTCTCGGTTATCAAT[C/G]TGAACTCCCTAAAGT	4703
rs189043507	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151638734	CTGGAATGATGGCAC[A/G]TGGCCCTGTGCACAC	4703
rs189051720	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151682188	ATGCAAATCAGTGGT[A/T]GCCTGGGGCTGAAGA	4703
rs189056008	snp	C/G/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151508601	CAGGTGCGGTCAGGG[C/G/T]TCCCAGCTATAGGAC	4703
rs189132567	snp	C/T	0.00835141	0.0640778	intron-variant	NEB	GRCh38.p7	2:151607165	TAAATAGAAATGGTC[C/T]TTTGTCTTTCTTATG	4703
rs189173573	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151691068	ATTAACCTTACCCTG[C/T]TGAAGCCTTACACAG	4703
rs189177176	snp	A/G	0.00993419	0.0697739	intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151507153	ATGGTCTGGTAGCCC[A/G]AGGGAAATTATTTGA	4703
rs189191274	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151488578	TTGAGTCCATGAAGT[C/T]GAGACTGCAGCGAGC	4703
rs189207492	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151564215	GCTGGAGTGCAGTGC[C/T]GTGATCTAAGCTCAC	4703
rs189211507	snp	C/T	0.00478085	0.0486577	intron-variant	NEB, RIF1	GRCh38.p7	2:151527095	GCATTTGATTAAACA[C/T]ACAGGGAGTCCTCTT	4703
rs189217946	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151546142	AGGCAGGAGCAAAAA[C/T]AATTGTCATTTAACT	4703
rs189232206	snp	C/T	0.00043097	0.0146731	missense	NEB	GRCh38.p7	2:151553454	CAGGAGTGTCCCAGA[C/T]GTAGCAACCAATGCC	4703
rs189243890	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151612064	ATGCTCTGTTAAAGG[C/T]CTGCATGAGAATCAG	4703
rs189256996	snp	C/T	0.00318978	0.0398085	intron-variant	NEB	GRCh38.p7	2:151649581	AGCAGTGTTGAGTAA[C/T]CTTTCCCTTCTTTGC	4703
rs189269744	snp	A/C	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151723646	CTTTCCATCCAACCC[A/C]AGTCATTTTTACTGA	4703
rs189270720	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151556162	GTTTCCTCCAGGTAA[A/G]AATTAAATAATTCCA	4703
rs189270971	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151617116	TAGGGGAAGGTTTTA[A/G]AAGTATAATTCCTAT	4703
rs189300215	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151654540	TTTATAAATTGCAAT[A/G]ATTTAGTTGCAATCT	4703
rs189304276	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151722426	AGGATACCAAAATTC[C/T]GGCAAGTGGGATCAC	4703
rs189366071	snp	A/G	0.00279162	0.0372561	intron-variant	NEB, RIF1	GRCh38.p7	2:151500352	TAAATTTTCCTAATG[A/G]CATTTGATTCTCCAT	4703
rs189370433	snp	A/G	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151648633	TGTGGGGGCTGCCCC[A/G]TGCATTGTGGGGTGC	4703
rs189385160	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151671786	ATCGAGTGCCAATAA[A/G]TGTATAACACTTCTT	4703
rs189391277	snp	G/T	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151690012	CTATGTTAGCACCTT[G/T]CTGTTCAAAGAGTAG	4703
rs189400576	snp	A/C	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151713262	AAAGCCAGTTAATTA[A/C]CCTTCTCTTTTTCTG	4703
rs189426770	snp	A/C	0.00279162	0.0372561	intron-variant	NEB	GRCh38.p7	2:151732678	ATTCTGAATATCTAA[A/C]CCATGTTACCCTATA	4703
rs189450215	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151569833	ATTCTATAGAAAGAA[A/T]ATTTTCACAGTTTTC	4703
rs189458281	snp	A/G	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151629445	AAAACAAGCCAATAA[A/G]TGTGCTTAAACTGGC	4703
rs189462757	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151611867	AAGACACGTAAGTGG[C/G]CTGAATCTGCTCTGC	4703
rs189511734	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151570486	CTGAGAAGTTAAAAA[A/T]GGCCACTCACGTCAC	4703
rs189538857	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151629773	TCAAGTTTCTGGCAA[C/T]AGTGGAAAGCAAATA	4703
rs189541265	snp	A/G	0.000408108	0.0142789	missense	NEB	GRCh38.p7	2:151562760	TCATCATGTCATTGG[A/G]GATATGAACATTTGC	4703
rs189541337	snp	A/T	0.00755907	0.0610114	intron-variant, utr-variant-3-prime	NEB, RIF1	GRCh38.p7	2:151497394	AAAACTCATTATTTT[A/T]AAAAAAAGATTGAAA	4703
rs189542576	snp	C/T	0.00636936	0.0560724	intron-variant	NEB	GRCh38.p7	2:151702383	GATGTCAATTAGGTC[C/T]GCTTGGTGCAGAGCT	4703
rs189550334	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151626262	TAAGACTAGAGGTGC[A/G]TGTCACCACACCCGG	4703
rs189553632	snp	C/T	0.000404367	0.0142134	missense	NEB	GRCh38.p7	2:151672679	GCTTCCTTGTATTTA[C/T]ACTGTGGAGGCAGAA	4703
rs189576481	snp	C/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151501049	CAGTATCTTTTCTTG[C/G]ATCTCTAACCCAGAA	4703
rs189609282	snp	C/T	0.00086911	0.0208279	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151526214	GAGGCGTGTCAGGTA[C/T]GGCATGGCAGGTTCC	4703
rs189615764	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151645338	TGTGAAATAGTCTGT[A/C]TCCCAAAATGGGACC	4703
rs189617624	snp	C/T	3.33367e-05	0.00408255	missense	NEB	GRCh38.p7	2:151666386	TGGCTTTCTCGTAGG[C/T]CTCCTTATATTTGCA	4703
rs189620546	snp	A/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151719313	TGTCTCAAGAGGAGA[A/T]TTATCTTTCTAATCT	4703
rs189623595	snp	C/T	0.00213086	0.0325713	missense	NEB	GRCh38.p7	2:151687639	ACATCGCTGGTGTTC[C/T]TGGTGTTGGCTTTGG	4703
rs189628263	snp	A/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151709390	ATAAATTAGGAAATA[A/T]TGAAGATGGTAATTA	4703
rs189655274	snp	A/G	0.00222593	0.0332868	missense, intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151499356	GGAGTGATGGGGATT[A/G]GAATCCCTTTTCCAA	4703
rs189655947	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	NEB	GRCh38.p7	2:151734790	GGCTTTAACCCTTCC[A/G]TGACTGCTTTCTTCA	4703
rs189663713	snp	A/T	0.00358779	0.0422022	intron-variant	NEB, RIF1	GRCh38.p7	2:151516925	AAACACTTTAAAATT[A/T]TTAATGCTATTAGCA	4703
rs189680878	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151534846	TGGCAGTAATTCTTC[A/C]GGGTTGTCCAGTCTG	4703
rs189696194	snp	A/G	0.0103295	0.0711199	intron-variant	NEB	GRCh38.p7	2:151557569	AGACACAACCAAAAA[A/G]GAGAATTTTAGACCA	4703
rs189775542	snp	A/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151677228	TGCCACAATAAAGTG[A/T]CTGGGATTTAAGCTT	4703
rs189789895	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151720037	GCCAAGAAGTTTCAG[A/G]CAAATCAGATCTAGA	4703
rs189798513	snp	C/T	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151539885	TGCTAGACACTTATA[C/T]ATTATCTTGTTTGGT	4703
rs189799843	snp	C/G	0.02016	0.0983543	intron-variant	NEB	GRCh38.p7	2:151545211	GCCATGCTCGGGGCT[C/G]CTGATAGCAGGAATT	4703
rs189808361	snp	A/G	0.0240643	0.107019	intron-variant	NEB	GRCh38.p7	2:151578372	TTTGATTCATAGCTG[A/G]AGGACCATGGACATT	4703
rs189814602	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151628762	AGTTACTTGGGAGGC[G/T]GAGGCAGGAGAATCA	4703
rs189829350	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151606501	TAGCACAGGATGAGA[G/T]GAATTCTATGCACAG	4703
rs189831062	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151640852	AAATATATATCTTAT[A/G]TAAAATATATACCAT	4703
rs189833374	snp	C/T	0.00478085	0.0486577	intron-variant	NEB	GRCh38.p7	2:151644327	ATCCTTGATCTTATC[C/T]TCATCCCACACTGCA	4703
rs189852571	snp	A/G	0.00438332	0.0466095	intron-variant	NEB	GRCh38.p7	2:151641811	ATTTTTAGAAATGTG[A/G]GCAAATCCTTTATTT	4703
rs189854512	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151660899	TAGGCCGATTGAGTA[C/T]TTGAAATGTAGCTAA	4703
rs189862776	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151684619	TCAGTTCTTCCTAAC[C/T]TTGAAGGGCATGCTC	4703
rs189874501	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151506326	AGTTCCTGGAGAAAG[A/G]CTAGGACACATGGCT	4703
rs189912759	snp	C/T	0.000952673	0.0218043	missense	NEB	GRCh38.p7	2:151560611	CTGGCCAGATGCTTC[C/T]GGTTCTTGGCGTGTG	4703
rs189918704	snp	C/T	0.00189956	0.0307599	intron-variant	NEB	GRCh38.p7	2:151541434	TGGCAGGCTTATGAA[C/T]CTCTGAGCTTACCTG	4703
rs189923104	snp	C/T	0.000807615	0.0200787	intron-variant	NEB	GRCh38.p7	2:151581633	AATTAGTAAATAAGT[C/T]AATTACCACATAAAT	4703
rs189946813	snp	C/T	0.00557542	0.0525036	intron-variant	NEB	GRCh38.p7	2:151623859	ATGTGCTTCAATCAT[C/T]TCATGGCTTCAGGCC	4703
rs190059793	snp	C/T	1.65908e-05	0.00288012	missense, intron-variant	NEB	GRCh38.p7	2:151644574	CCCATTCGGTAGAGT[C/T]TCTGTTAAGAAATGA	4703
rs190063063	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151489890	TGGTTAAAAAAAACC[A/G]TAATACCTAATACTT	4703
rs190067734	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151559246	CCACAATGAGATACC[A/C]TCTCACGCCAGTTAG	4703
rs190067778	snp	A/G	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151622855	CAATGTTGCTTTTCT[A/G]TCCAGAATTCAGTTC	4703
rs190073570	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151648026	TTTCTCATATAGATA[C/T]ATAGATATAGATCTG	4703
rs190078692	snp	A/G	0.00517822	0.0506191	intron-variant	NEB	GRCh38.p7	2:151730123	TAAATGGATTGCATC[A/G]TGGAAATAATAAGAT	4703
rs190080213	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151729267	TGCCAATCACAAAGC[C/T]AAGGCTCCTTGGCTT	4703
rs190080587	snp	A/T	0.00478085	0.0486577	intron-variant	NEB	GRCh38.p7	2:151687012	CATTACTAAAGTCAA[A/T]GAAGAACGATACTCT	4703
rs190098609	snp	G/T	0.000463134	0.0152103	intron-variant	NEB, RIF1	GRCh38.p7	2:151507991	GCTGTGCCTTACATT[G/T]AATAAAAACTTACAA	4703
rs190099660	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151687928	AAATAAGTATCAACT[A/T]CTCTTTTTAATGTTC	4703
rs190100490	snp	A/G	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151555441	TGCGAGATTAAAACT[A/G]TGCTTAGGAATATCT	4703
rs190103999	snp	A/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151710594	GAATTGACAAATAAG[A/T]CAGCAAATTAAGAAA	4703
rs190104505	snp	G/T	0.000533686	0.0163266	intron-variant	NEB, RIF1	GRCh38.p7	2:151512708	GATTGGGGTTTATGA[G/T]TGATGGCATGACGAA	4703
rs190106012	snp	A/G	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151657772	GATCTCATGAGTCAG[A/G]GAGCTGACATCTATG	4703
rs190108219	snp	A/G	1.65905e-05	0.0028801	intron-variant	NEB	GRCh38.p7	2:151680722	ATATAGATAGCATTA[A/G]CACTTACATCACTCC	4703
rs190127469	snp	A/C	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151522492	ATACATTAGGAGTCC[A/C]TCTCTGAGTCTAGTC	4703
rs190132249	snp	A/T			utr-variant-3-prime, intron-variant	NEB, RIF1	GRCh38.p7	2:151485559	CTCTAGGCACAGAAA[A/T]AATATTGCAGAAGCT	4703
rs190160163	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151558066	TTCAATTAGGAAAAG[A/G]GGAAGTCAAATTGTC	4703
rs190169784	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151536064	GGTTGTACACCACCA[G/T]GCCTGGCTAATTTAC	4703
rs190182350	snp	C/T	0.000399281	0.0141238	missense	NEB	GRCh38.p7	2:151576318	GGGGCATCCAGCCAA[C/T]GCCACGCAACCACTC	4703
rs190190974	snp	C/T	0.0119091	0.0762411	intron-variant	NEB	GRCh38.p7	2:151637624	TGGCAGCCGAGTAGC[C/T]GCACTAACACATCTC	4703
rs190193237	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151618998	TGATAAGTATTAGAC[A/G]ACTGGTTTCGAAAAA	4703
rs190253948	snp	C/T	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151630171	CCATAATCACAACTT[C/T]CTAAATTTTGGTTGT	4703
rs190270930	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151650098	CTTTGTGGTTCTACT[A/C]ATTTATTAAGCAAGT	4703
rs190304350	snp	G/T	0.0221141	0.102801	intron-variant	NEB, RIF1	GRCh38.p7	2:151510848	TCCTAAATTTGTGAG[G/T]CAGCTTACATTGCTT	4703
rs190308758	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151626600	GGAGTGCAGTGGCGC[A/G]ATCTCAGCTCACTAC	4703
rs190311687	snp	C/T	0.00636936	0.0560724	intron-variant	NEB	GRCh38.p7	2:151660623	AGATTGGCAAACTTT[C/T]TCTGTATAGACAGAA	4703
rs190314267	snp	G/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151487075	CATGTGCGTGTGTGT[G/T]TACTGACAGAAAAGA	4703
rs190317746	snp	A/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151530440	GATCCTAGGTTTTAA[A/T]GTGACTAAGGCCAAA	4703
rs190319656	snp	A/C/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151494793	AGCTGGGATTACAGG[A/C/T]GTGCACCACCATGCC	4703
rs190322907	snp	A/G	8.50521e-05	0.00652065	synonymous-codon	NEB	GRCh38.p7	2:151665498	TATGGGCACCCAGCC[A/G]ATCCCTTTCATCCAA	4703
rs190335341	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151705277	TGATTAGTTTTAAAT[A/G]TGCAGCTGATAAAGC	4703
rs190336010	snp	A/G	0.00265065	0.0363084	synonymous-codon	NEB	GRCh38.p7	2:151553828	AAGTCACAGGCTTAC[A/G]TCGCTGATCTGATCT	4703
rs190336699	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151708941	CTGGTCCAAAACACC[A/G]TCTTACACGTGGATG	4703
rs190337294	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151529985	ACCAGCTCACCCAGA[C/T]AGAATTAGTCTTGCT	4703
rs190345918	snp	A/G	0.00318978	0.0398085	intron-variant	NEB	GRCh38.p7	2:151612848	ATGTGTTTTTTTGGG[A/G]ATAAAAACGACGTCT	4703
rs190348020	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151571104	TCTGCCTCCCAGGCT[C/T]AAGCCATTCTCCTTC	4703
rs190350909	snp	C/T	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151706735	AGGGACTCATGCCTT[C/T]CTGTGGTTACATAGT	4703
rs190359096	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151726825	GTGGCCAGGAGTTTA[C/T]GACCATCCTGGGCAA	4703
rs190360492	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151532002	ATGGTATCTAGCTTT[C/T]TCTTTAATTCCTAAC	4703
rs190364700	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151573331	AATGGTAAGGTTCTG[A/G]TGTTTTCAGCTGAGA	4703
rs190418561	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151496579	AGCAGGGACCTCAGC[C/T]GCTGGGGAAAGGCTG	4703
rs190419780	snp	C/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151493541	TCATGTTATGGCTCA[C/G]TTATATCACACTGAA	4703
rs190493045	snp	A/G	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151725327	GGTTCATGCTTTTCT[A/G]GATTTGTGAACTAGC	4703
rs190503847	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151678742	CTTCCTCAGAGATAT[A/G]TGGAGGGCACTGTGG	4703
rs190510381	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151628012	AGCACTAATCTAATG[C/G]GCAGTAGTCTAATGC	4703
rs190514184	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151696355	GCCACCCAGACATCA[A/G]TGACAGAGCTAACAT	4703
rs190559725	snp	A/G	0.00478085	0.0486577	intron-variant	NEB	GRCh38.p7	2:151641578	TTAAGTGATCCTCCC[A/G]CCTTGACCTCCCAAA	4703
rs190561841	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151490827	ACCAAAATGAATAAA[C/T]AGTAATATTCACATT	4703
rs190566569	snp	A/C	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151528282	GCCTGCACTATTAGG[A/C]ACATTTCTTTCCTCA	4703
rs190576077	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151684215	GGTAAATTTATGTTA[C/T]ATGTATTTTGTCACA	4703
rs190576328	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151566489	TTCCCTTTTGTTAAT[C/G]ATGAGAAGACCCAGG	4703
rs190584571	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151548909	TAGGTTTGATTCCCA[C/G]GAATATGAAGGGTAG	4703
rs190586690	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151609241	CAAGTGTTAGACATA[C/T]AAATCCTTAGCTGAA	4703
rs190590883	snp	C/T	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151636027	AGTTTTCACAGAAGA[C/T]GCTGTGTCCTGTAGG	4703
rs190594778	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151656492	TATGAGTTTTTACAC[A/G]GAGCAATTCCTTTGA	4703
rs190601529	snp	G/T	0.00318978	0.0398085	intron-variant	NEB, RIF1	GRCh38.p7	2:151509615	GGGAGGAAGAGAGGT[G/T]TTTTTTTTGTTTGTT	4703
rs190603389	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151547358	TCAAAGACCACTGGT[A/T]GTTTTAACTGCTGAA	4703
rs190605644	snp	A/C	0.000374581	0.0136803	missense	NEB	GRCh38.p7	2:151552757	TTCCTTGTTTTCAAC[A/C]TGTGAGCTTTATACT	4703
rs190717362	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151734211	GCAAAGGACTTGACT[C/G]TAATCACACACGGTA	4703
rs190745431	snp	C/T	0.00279162	0.0372561	intron-variant	NEB	GRCh38.p7	2:151674344	AAAGTGACAGGTTTT[C/T]CCAAACAATATTTTG	4703
rs190747291	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151729707	CAAAGCAGAAACCAC[C/T]TCTCCTCTGCCTCAG	4703
rs190759199	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151692532	GGTAGAGGCTCATGC[C/T]TTATATAATCTCATC	4703
rs190765209	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151716092	AAAAAGATAAATTGT[C/T]CTTCTCCCGTCTTAT	4703
rs190784493	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151615965	TATTTGTCAACATCT[G/T]TGAATAAGAAATGGC	4703
rs190788190	snp	A/C/G	0.000287767	0.0119917	intron-variant	NEB	GRCh38.p7	2:151694493	ATGTCCCCGAAGCCA[A/C/G]CCTGTCCAGGTCCCC	4703
rs190800576	snp	C/G	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151651365	TATGGAAATGATAAT[C/G]CTTACGGGCTAAATG	4703
rs190816134	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151726457	TCAATAGGATGCTTT[C/T]GACATAAACTTTAGT	4703
rs190823348	snp	A/C	0.00358779	0.0422022	intron-variant	NEB	GRCh38.p7	2:151631018	ATTTAGAGGATTTCA[A/C]GCATGTAATTTAAAA	4703
rs190843599	snp	G/T	5.53429e-05	0.00526007	intron-variant	NEB	GRCh38.p7	2:151650546	ATATGAATTAATATA[G/T]AAACTATTGGATTTA	4703
rs190848612	snp	A/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151524303	ACCAGTGCACCCATC[A/T]GCATTACCTGGCTGC	4703
rs190857199	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151527357	CCCAACCATCCTCCT[C/T]TCCTTCTCGGATCTC	4703
rs190909511	snp	A/G	0.00438332	0.0466095	intron-variant	NEB, RIF1	GRCh38.p7	2:151486722	CATGATACAACATGG[A/G]TGAACTTCAAAAGTA	4703
rs190915366	snp	A/T	0.00199481	0.0315187	intron-variant	NEB, RIF1	GRCh38.p7	2:151488838	TTGCTGATTTATAAT[A/T]CTTTTAGGGTCTGTT	4703
rs190983049	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151716425	TACAGGTGTGAGCCA[A/C]CGCGCCTGGCCAATA	4703
rs190990358	snp	A/C	0.00199481	0.0315187	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151503051	TTAATGATGAACTCT[A/C]CAATGCTAATTCTGG	4703
rs190999546	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151688855	TAAAGAAGGGACAAA[A/G]GGGGATGGTGTGAGA	4703
rs191005974	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151711246	TATGCGGTTTTGAAA[C/T]ACCTTGGCTGAAGTG	4703
rs191006696	snp	C/G	0.00119737	0.0244387	utr-variant-3-prime, intron-variant	NEB, RIF1	GRCh38.p7	2:151485694	AGGTAACAGTGGAGA[C/G]TCTAAACCGAAACAT	4703
rs191012906	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151541114	TCAACATATTTTCCC[C/T]TGATTTTTGCGTGAC	4703
rs191025448	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151523556	AGTCCTATAGGATCA[A/G]ACTTGCACTCTGATA	4703
rs191051682	snp	A/G	0.00835141	0.0640778	intron-variant	NEB	GRCh38.p7	2:151632631	CAGTAATCCGAGATC[A/G]CGCCACTGCACTCCA	4703
rs191054016	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151697794	AATTGAGGCCAGGTG[C/T]GGCGGCTCACGCCTG	4703
rs191058825	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151730732	AGATGCAAAATTTCC[C/T]TCAATGGCCTGCATT	4703
rs191066110	snp	C/T	0.00557542	0.0525036	intron-variant	NEB	GRCh38.p7	2:151675205	TGGGCCTAAATAAAT[C/T]GTCAAGGCACCATCC	4703
rs191083610	snp	C/T	2.28877e-05	0.0033828	synonymous-codon	NEB	GRCh38.p7	2:151565800	GCCTCGGAGCCACTC[C/T]AGGTCAGCTCTGTAG	4703
rs191097958	snp	C/T	0.0013596	0.0260375	intron-variant	NEB	GRCh38.p7	2:151627238	AAAAGCGAGTATTAC[C/T]GAAGTTGTTTTAACA	4703
rs191118542	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151667648	TCCTCCCATCTCAGC[C/T]TCTCAAATAGTTGGA	4703
rs191158721	snp	A/T	0.00318978	0.0398085	intron-variant	NEB, RIF1	GRCh38.p7	2:151528009	AATTAAATGAATTAT[A/T]AAATTTTATAAAATT	4703
rs191163375	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151503647	CTTTGAAAACTGGGC[A/G]CTAAATTATGCATTT	4703
rs191204814	snp	A/T	0.00438332	0.0466095	intron-variant	NEB	GRCh38.p7	2:151728405	TTAGGCATTCTCCAC[A/T]GTAGTAGGAGACAAA	4703
rs191239070	snp	A/G	0.00358779	0.0422022	intron-variant	NEB	GRCh38.p7	2:151686225	AAAATGTTGTCAAAG[A/G]TCCAAATGGCTTTAA	4703
rs191247719	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151707774	TCAAGGAATCCTAGA[C/T]AAATCTACCACTTAT	4703
rs191299444	snp	C/G	0.0103295	0.0711199	intron-variant	NEB	GRCh38.p7	2:151605717	ACATGATGAAAATCA[C/G]AGAAGAACACAGAGA	4703
rs191301938	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151562429	ATTAAATATTTAACA[C/T]ATGTGTCCTATGGCT	4703
rs191305748	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151626050	AGTTTATTAGCTGCA[A/C]ATGTACCTGTATGTG	4703
rs191308706	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151722393	TTAAGTTCCTCTAAC[A/G]TACAGTTTTCAAGGT	4703
rs191320701	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151643634	GAGGCTTCCACCAAA[A/G]CAATGGGGCTTTGCT	4703
rs191326683	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151664110	AATTGGTTTAGAGAG[A/G]TTTAGAAAGCAGATT	4703
rs191344391	snp	A/C	0.0825414	0.185628	intron-variant	NEB	GRCh38.p7	2:151609025	TCTGAGTACATGCAA[A/C]GGCAAAGCAAAAATA	4703
rs191354219	snp	C/T	0.00517822	0.0506191	intron-variant	NEB	GRCh38.p7	2:151673862	CCTCAGCCTCCCTAG[C/T]AGCTGGGACTACAGG	4703
rs191354245	snp	G/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151583944	TACGATTTTGGGTCA[G/T]TTCAGAGAGGACATG	4703
rs191357992	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151642128	GCAAATATTTGTAAC[A/C]CACCACCTGATATAG	4703
rs191358881	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151645717	CAATGATAATGACAA[C/T]AAAAATGAGATTCTC	4703
rs191411275	snp	C/T	0.00716266	0.059414	intron-variant	NEB	GRCh38.p7	2:151548125	AGTCTCTCCAAGGCA[C/T]TACCAAATACAAAAA	4703
rs191421788	snp	G/T	0.00716266	0.059414	intron-variant	NEB	GRCh38.p7	2:151542246	CTGGTTCTGCCCTCA[G/T]GCAAAGGCTGCTGTT	4703
rs191423579	snp	A/G	0.0209421	0.100162	intron-variant	NEB, RIF1	GRCh38.p7	2:151504531	ATAAGCAGAGAGTGA[A/G]AAGGGAATGAGATCT	4703
rs191479433	snp	A/C	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151495890	CTGAAGTCATTGACA[A/C]AAAAACACAACAAAA	4703
rs191482613	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151683029	TCTAATTCCAACCTG[C/G]AAAATGTTCGAGTCA	4703
rs191487260	snp	C/T	0.00119737	0.0244387	intron-variant	NEB, RIF1	GRCh38.p7	2:151511707	AAGTGAAGGCCTATC[C/T]CAGGGTGTGAAGGAT	4703
rs191490930	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151702750	TCCTTTTATTTTGAG[C/G]CTATGTGTGTCTCTG	4703
rs191507607	snp	A/T	0.0023933	0.0345097	intron-variant	NEB, RIF1	GRCh38.p7	2:151531403	TTCACTGCAACCTCC[A/T]TCTCCTGGGCTCAAG	4703
rs191569384	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151731468	AAAGCTAGTTCCTCT[C/T]TGTTTTCTAAAATCT	4703
rs191576590	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151659641	CTTATTCAAACAATA[C/T]AGCAGGGAGGATGTA	4703
rs191576710	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151711828	TTACTATTGTCATCA[C/T]CATAACAGAAAGAAA	4703
rs191579691	snp	A/C/T	0.000229728	0.0107153	missense	NEB	GRCh38.p7	2:151561212	GGAAGACGCACCTCA[A/C/T]TGGCATTAATGCCAC	4703
rs191587678	snp	A/G	0.00953873	0.0683987	intron-variant	NEB	GRCh38.p7	2:151625336	TGTGTCTGTCTGTCT[A/G]TCTGTCTGTCTAATC	4703
rs191596517	snp	A/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151646373	ACAACATAAGCAGAA[A/T]ATAGATGCAATATTT	4703
rs191607728	snp	A/G	0.000398585	0.0141115	intron-variant	NEB	GRCh38.p7	2:151692236	AAAGCCCTCCTACCC[A/G]AAAGGTAACCGTGGC	4703
rs191610670	snp	C/T	0.00159662	0.0282093	synonymous-codon	NEB	GRCh38.p7	2:151688364	TATATGGCACTTGAA[C/T]TTCTCACCTTCATGT	4703
rs191619875	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151662417	GTGTGTTTAACATTC[C/T]GTAACTTCCATTTCA	4703
rs191626993	snp	C/G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151733866	CCTTAGCCTAAGCTT[C/G/T]TAATGCAGAAAACAG	4703
rs191633535	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151730509	AGGAGAGAGGAATCC[C/T]GTCCTTAGCCTCACC	4703
rs191633560	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151557076	AAATCAATGAATCCA[A/G]GAGCTGTTTTTTTGA	4703
rs191676595	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151618491	ATTCTGCAGATCAAC[A/C]GATAAGAAACAGATT	4703
rs191681154	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151524785	GATTCTTCTGCCTCA[A/G]CCTCCCGAGTAGCTG	4703
rs191696329	snp	A/G/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151509209	GCCTAGATTTTGTTC[A/G/T]TCTAAATGGAAGCGA	4703
rs191711599	snp	C/T	0.0015146	0.0274773	intron-variant	NEB, RIF1	GRCh38.p7	2:151492531	ATGAGTGGTGCTGTC[C/T]TAAATCTGAAACCTC	4703
rs191721976	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151516171	ATTCATAAAGGAAAA[C/T]CCAAATTACATTCAG	4703
rs191722579	snp	A/T	0.000348094	0.0131881	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151529281	CAATGGTGCAGTTGG[A/T]TTTATTTCTTTGGTA	4703
rs191833711	snp	C/G	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151708669	TCTCCCCTGAAACTT[C/G]AGGCTCATGTAGTCG	4703
rs191861842	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151652332	CCAAGCTCAAGTGAT[C/T]CTCCCACCTCAGCCT	4703
rs191875178	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151675814	TAAAAACTTTCCAAA[C/T]TATAATTGTATCAGT	4703
rs191885809	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151623463	AATAATTAAACTTCA[A/T]TTTTATACCCCATTC	4703
rs191891809	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151530933	ACTGGACCAGGGTTT[A/G]TTACATCTCATTAGA	4703
rs191894959	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151668109	AACTGTATACACAGT[A/G]TAATCTCAACTGATC	4703
rs191895957	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151572128	GGAGTTTGAGACCAG[C/T]CTAGCCAACATGGTG	4703
rs191901936	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151531758	GCAGATGCCCCCTGA[A/G]TTTGAGAAGGTATTC	4703
rs191913719	snp	G/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151710896	AACCTGAGATTTCTA[G/T]GCCAAATGAACTTAG	4703
rs191918237	snp	A/C	0.00199481	0.0315187	intron-variant	NEB, RIF1	GRCh38.p7	2:151512350	CTCTCTTTTTTTTTT[A/C]AGAGTCTCACCCTGT	4703
rs191918431	snp	C/T	0.00279162	0.0372561	intron-variant	NEB	GRCh38.p7	2:151555217	GATACAGCAGTAGCG[C/T]CTGCCATGGGGTTAT	4703
rs191932021	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151616410	AAATTATTTACTGGC[C/T]GGGCGTGGTGGCTCA	4703
rs191935844	snp	C/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151534446	TCCCAACATACCCAA[C/G]ACAATAAAAACAGGG	4703
rs191938959	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151572925	GTTTTCAGCTACTAA[C/T]TTTGAGAACATGGGA	4703
rs191940349	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151574752	TATTTATTTATTTGA[A/G]ACAGGGTCTTGCCCT	4703
rs191941623	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151632775	TATGAAGGTCATATC[A/G]CAGGGTGAGGAAGGT	4703
rs191960837	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151495306	ATAGTGATTCTCAAC[A/G]TGGGGTCCTTGGACA	4703
rs192031676	snp	G/T			intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151498573	AAATAGGAAAAGAAA[G/T]GTTGTTATTTTCATT	4703
rs192047179	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151721662	TATAAATTCTAAGAG[A/G]AAAGGATGAAAACTG	4703
rs192094279	snp	A/C	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151575644	ATGCTCATAGTATAG[A/C]CCTGACTGGGTAACT	4703
rs192098032	snp	C/T	0.00448558	0.0471452	missense, intron-variant	NEB	GRCh38.p7	2:151636277	CGATGGGGATGGCGT[C/T]GCTTCGCAAGTCATA	4703
rs192110787	snp	C/T	0.00318978	0.0398085	intron-variant	NEB	GRCh38.p7	2:151648248	AACTTGTCCATTTCC[C/T]TTTGAGGTATGCAGC	4703
rs192114549	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151698083	AACAAAACAAAACAA[A/G]ACAAAACAAAACAAA	4703
rs192117840	snp	C/T	0.000347777	0.0131821	missense	NEB	GRCh38.p7	2:151679792	TCAGGTCATATCCCT[C/T]CTTGCTCAAGTCTTT	4703
rs192120847	snp	C/T	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151722694	GACTACAGGCATGCA[C/T]CCCCACACTTGGCTA	4703
rs192159441	snp	A/G	0.00199481	0.0315187	intron-variant	NEB, RIF1	GRCh38.p7	2:151529767	CTCGTGACCTCAGGT[A/G]ATCCCGCCCACCTCA	4703
rs192161410	snp	A/G	0.0189856	0.0955633	intron-variant	NEB, RIF1	GRCh38.p7	2:151508798	TCCTTGGGCTCCCCT[A/G]TCCTGCCCCAGCCTT	4703
rs192176986	snp	C/G	0.0194118	0.0965871	intron-variant	NEB	GRCh38.p7	2:151551520	TAACTTGTAAATATT[C/G]CTAAAACATGCCCAT	4703
rs192184171	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151611047	GAAAGTAAAACATAG[C/G]AATATTTAAATAGCT	4703
rs192186947	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151658210	CAGAATGCTTCGTTG[A/G]TGCTTCAGTGGCTGA	4703
rs192187173	snp	A/G	0.02016	0.0983543	intron-variant	NEB	GRCh38.p7	2:151554095	GGCCATACATGAGAA[A/G]TCAGGCTAACCAACT	4703
rs192188977	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151569493	AAGGAGGACATACTC[A/G]AGCAGCCACGCAGGT	4703
rs192205315	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151628866	AGACTCTGAGACTCT[G/T]TCTCAAACAAACAAA	4703
rs192217338	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151613270	GTTTTCAAGTTTCTT[A/G]GAAAATTTGTCTTCA	4703
rs192246661	snp	C/T	0.00279162	0.0372561	intron-variant	NEB, RIF1	GRCh38.p7	2:151509459	GAGCTGGTGCTAATC[C/T]CTTAGAGGGATAATC	4703
rs192270760	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151511104	CACTGGGATAGGTCC[A/G]CATGCTGAAGCTTTC	4703
rs192346354	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151694158	TCAAAGGCATCAACA[A/G]GAATAAGGAAGTTCA	4703
rs192355519	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151718442	AGCCCATTATGAGTC[C/T]CTGGTTAGTCCCTAC	4703
rs192356492	snp	C/G	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151625921	CAGGTCACTCTCACC[C/G]CAATTAAATAAAAAG	4703
rs192400461	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151525133	ACTGCTTCAAATGGG[C/T]CCCCAAGAGTGTTGA	4703
rs192402741	snp	C/G	0.00678339	0.0578418	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151525997	CTTGACGTGAACAGT[C/G]TCCCGGGTCTCTGGT	4703
rs192411508	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151487970	ATGATATTTGATTCA[A/G]TTTGATACTTTGTAT	4703
rs192413758	snp	G/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151505007	ACATGTCTACCCAGG[G/T]TCTTTTTGGACACTG	4703
rs192420192	snp	C/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151554725	CTATGTTTAGATACA[C/G]AAATACTTGCCACTG	4703
rs192421493	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	NEB	GRCh38.p7	2:151735999	TAAAGTAAAAAATGA[A/G]CATTGACCTTCTTAG	4703
rs192423523	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151653478	TAAGCCCTTGGGAAC[G/T]TAAACCTAAATTTCT	4703
rs192425425	snp	G/T	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151561556	CCTATTCTCCATCCC[G/T]GACAGCAGCCCCTCA	4703
rs192431887	snp	C/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151543712	GGCTGGCCTCAAACT[C/G]CTGCACTCCAGTGAT	4703
rs192432310	snp	A/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151675903	TCAAAAGGCTCACTA[A/T]TTCATATTTGCCCTA	4703
rs192441239	snp	A/C	0.00795532	0.062565	intron-variant	NEB	GRCh38.p7	2:151605373	ACATTAGGTCAAATG[A/C]TCTCCTAAGAGTACT	4703
rs192459112	snp	C/T	0.00438332	0.0466095	intron-variant	NEB	GRCh38.p7	2:151618869	CACTTTTATTTCCAT[C/T]TTCAAAAATCACAAA	4703
rs192478649	snp	A/G	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151487580	GAATTTCACATTTTA[A/G]TAATATCACGAATTA	4703
rs192489739	snp	C/T	0.00716266	0.059414	intron-variant	NEB	GRCh38.p7	2:151656537	AGTGTCAATATGCTA[C/T]ATTATTTTTGTATAA	4703
rs192510362	snp	G/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151696928	CTTTCCTATATCTTC[G/T]GGTTTCCAATAACTC	4703
rs192559143	snp	A/C	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151529066	TTTATATTTTAGCAT[A/C]ATTGTTCATGCTCCT	4703
rs192569351	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151492024	ATGTTTTGACTTGAT[A/G]TAGGTAATGCTACTT	4703
rs192589367	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151628656	GACCAGCCTAGCCAA[C/T]ATGGTGCAACGCTGT	4703
rs192599031	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151670345	CTTTCTGGTGGAGGC[A/G]TTTTAACAGAACTCT	4703
rs192610117	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151668494	AAAAATTAACAATTT[C/T]ATCCAAGTTTTATTA	4703
rs192653230	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151521249	TCACAATGCTGAGAC[C/T]CCTTTACTTTGAATA	4703
rs192666140	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151537540	AGAGCTGAACTTTCT[A/C]AGTGAGCATTGTTAT	4703
rs192669125	snp	A/G	0.00557542	0.0525036	intron-variant	NEB, RIF1	GRCh38.p7	2:151500633	CAGGGTCTCACTCCT[A/G]TTGCCTAGGCTGGAG	4703
rs192680024	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151628465	AAAAGCATTTTGTTG[G/T]TGGTGGTGGTAAGGG	4703
rs192681908	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151558468	TAGATTCAATGCTAT[C/T]CCCATCAAGCTACCA	4703
rs192691122	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151646968	AGTTATGCCTCATAA[C/T]CATTGTGAAGGATTA	4703
rs192693221	snp	A/G	0.00159617	0.0282053	intron-variant	NEB, RIF1	GRCh38.p7	2:151499582	GTGAAATATCAGTGT[A/G]TTTGATATTCATCAT	4703
rs192696802	snp	C/G	0.00398564	0.0444627	intron-variant	NEB	GRCh38.p7	2:151577604	GTTTGCCTTTGAGAC[C/G]GAGTCTCACTCTGCC	4703
rs192716842	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151544200	TGATGCACAACTTGC[C/T]CAAAATCCCTCTGGG	4703
rs192754055	snp	G/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151505376	CACAACATCCCCAAG[G/T]CATGGAAGCTCTTGA	4703
rs192758522	snp	A/C	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151607131	ACATAGATATCATAC[A/C]TAGCCCGCCATCTGG	4703
rs192761288	snp	A/T	0.00755907	0.0610114	intron-variant	NEB	GRCh38.p7	2:151572525	TATATATATATAAAA[A/T]ATATATATAAAAGTA	4703
rs192766711	snp	A/C/T	1.66197e-05	0.00288263	intron-variant	NEB	GRCh38.p7	2:151644446	GCAATCAAATCAATA[A/C/T]CAACAGAGGATAAAA	4703
rs192769920	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151716922	GAGCTAGTTTACTGC[C/T]TAAATATAGGTAGAC	4703
rs192774814	snp	C/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151686837	GCAAAATGTTACATG[C/G]CCCATAGATGAGCCT	4703
rs192826362	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151724038	CCCCTCTGCCCCCAG[A/G]TTGCTCAGGTTCCCA	4703
rs192843524	snp	C/T	0.00107724	0.0231831	missense, intron-variant	NEB	GRCh38.p7	2:151609823	CATCACTCTGCAGGT[C/T]ATAGGCCTTTTTTGC	4703
rs192848765	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151647400	CAGGTGTGAGCCATC[A/G]TGCCCGGCTAAAACT	4703
rs192857636	snp	C/T	0.00358779	0.0422022	intron-variant	NEB	GRCh38.p7	2:151689361	AGGCATGTGCCACCA[C/T]ACCCAGCTAATTTTT	4703
rs192871991	snp	G/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151519834	GGAATTGGGGAATAG[G/T]AGAAACACAAATGCC	4703
rs192887477	snp	A/G	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151550772	ACCTCCCAAGTAGCT[A/G]GGACCACAGGTGCAT	4703
rs192888796	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151689805	GCTGTTCTTTATTGG[A/G]ACACAAAATATTAAG	4703
rs192909346	snp	C/T	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151558369	GGAACTAAGAGAGGA[C/T]ACGAACAAATGGAAA	4703
rs192910192	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151619309	AAATTGTAGTACCTC[C/T]AATGGGAAACTCCTT	4703
rs192951371	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151520316	CTGAGTAAACAAATA[C/T]GAGAGTTTGGGGGTT	4703
rs192964949	snp	G/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151626566	TTTTGAGACGGAATC[G/T]TGCTCTGTCGCCCAG	4703
rs192974246	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151693889	GAGTTTATGCCTTAT[A/G]TAGTTTTTCTTACTT	4703
rs192975308	snp	A/G	0.00438332	0.0466095	intron-variant	NEB	GRCh38.p7	2:151664939	AAGAGGAAGAGATTT[A/G]CAACTCCATGGTAAA	4703
rs192992474	snp	C/T			upstream-variant-2KB	NEB	GRCh38.p7	2:151735205	CCCAGAAGCAACGTG[C/T]GAATGCGGACACAAA	4703
rs193025560	snp	C/T	0.00398564	0.0444627	intron-variant	NEB, RIF1	GRCh38.p7	2:151496195	GTTGTCTTTAAAAAG[C/T]AGGATTAATATGTAT	4703
rs193026977	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151573367	ATCATGCAAAAGAGA[A/G]CATATGTGACTTTCC	4703
rs193038729	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151663312	TCCATTTGCTGTTGT[A/G]GAATTCAGAATCCAA	4703
rs193042896	snp	C/G/T	0.00441203	0.0467612	missense, intron-variant	NEB	GRCh38.p7	2:151633722	GCAGGCATGTCCACT[C/G/T]GTGCAGGTAGTTCTT	4703
rs193058425	snp	A/G	0.00119737	0.0244387	intron-variant	NEB, RIF1	GRCh38.p7	2:151496607	CTGTCAGAGTTATCC[A/G]TGTTATTTTTTTTCA	4703
rs193127495	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151639467	CCACAAAAACTTTAT[A/T]AAAAAAAAGAAAAGG	4703
rs193128616	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151712633	AGGAGGAGGCTGGAG[C/T]TTGCTGGCTACTGAG	4703
rs193132406	snp	G/T	0.00597247	0.0543191	intron-variant	NEB	GRCh38.p7	2:151682220	GAGAGCTGAAATTTT[G/T]GGGGGAAACTTTTTG	4703
rs193136587	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151723165	GTTTGCCACCTATAA[A/G]AAGAGGGAACTGGAC	4703
rs193139751	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151550334	TGCCCAGTTGGCTGT[A/G]TGGCATCTAGCAAGA	4703
rs193155908	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151577109	GCTTTCTAGTAAGTT[C/T]TCTACACAGCAGCCA	4703
rs193161727	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151638409	CGCAGCTTGGGATAT[C/T]GGATTTGAAGGTGAA	4703
rs193176875	snp	C/T	0.00199481	0.0315187	intron-variant	NEB, RIF1	GRCh38.p7	2:151500184	AGGATTGTTAGTGAA[C/T]AGTAATTAAAAAACA	4703
rs193178265	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151536662	AGATGTTTTATTTAC[G/T]ATCTGGCATTTTTCA	4703
rs193218477	snp	A/C/T	0.00016787	0.00916035	missense, intron-variant	NEB	GRCh38.p7	2:151642588	CTTCACTTGCAATAT[A/C/T]TCTGGAGGCCTTGGC	4703
rs193221910	snp	C/T	0.00636936	0.0560724	intron-variant	NEB	GRCh38.p7	2:151616647	TGCAGTGAACCAAAA[C/T]TGTGCCACTGCACTC	4703
rs193222660	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151685540	GTTCAATTGGGGCAA[A/C]AATTTAAAAGAAGCT	4703
rs193224180	snp	A/G	0.00190648	0.0308157	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151503408	GAGTCACAGTGGTTG[A/G]AATGCCTGTTCCCAA	4703
rs193227711	snp	A/C/T	3.46736e-05	0.00416363	missense	NEB	GRCh38.p7	2:151727890	GTTGTCGTAGTCTCA[A/C/T]AAATTTTTGTTATTG	4703
rs193238639	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151555556	CAATCAACTTCTGTG[C/G]GATAACAATTAGTTC	4703
rs193239623	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151513156	ATAAGCAAAAGACCC[A/G]TACCAATGAGCATTA	4703
rs193281402	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151658984	ATTCACTCTCATAAC[A/T]GAGAGAGATATTAAT	4703
rs193295412	snp	A/C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151566721	TTCTCTTTTGCTTTG[A/C/T]GAACAACTTCATAAA	4703
rs193300993	snp	C/T	0.00160347	0.0282695	intron-variant	NEB	GRCh38.p7	2:151621056	AGTAGCTTTTAAATA[C/T]AGAATTCACATTCAC	4703
rs199498034	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151638811	TTTCTCTCTCTCTGT[C/G]TGTGTGTGTGTGTGT	4703
rs199505117	in-del	-/TG	0.02016	0.0983543	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151506742	ATTTCAAATGGTCTC[-/TG]GAGATGATTTTGGAG	4703
rs199511221	snp	C/T	0.000366801	0.0135376	missense	NEB	GRCh38.p7	2:151677916	TTAGACAGCTCCAGG[C/T]CCATGGCGTCAGGCA	4703
rs199521496	snp	C/G	0.00399193	0.0444975	missense, intron-variant	NEB	GRCh38.p7	2:151579446	ATCACTTGCCAGTGC[C/G]TGACCTTCTTTGGCA	4703
rs199527028	snp	C/T	0.499087	0.0213463	intron-variant	NEB	GRCh38.p7	2:151702203	CTTAATCCTGAGTTC[C/T]AGTTTGATTGCACTG	4703
rs199528953	snp	A/G	0.000298949	0.0122223	synonymous-codon	NEB	GRCh38.p7	2:151692285	GTTCTTCAGCTGAGT[A/G]TCAAGTTGATATTTT	4703
rs199543107	snp	A/T	0.178465	0.239547	intron-variant	NEB	GRCh38.p7	2:151675775	GAGAGAAAGTAGTAG[A/T]TAGAATAAGTTTTTC	4703
rs199551865	snp	C/T	0.00026763	0.0115648	missense, intron-variant	NEB	GRCh38.p7	2:151617429	CAGGCATGACATGAA[C/T]AGTTTTCTTGTCATT	4703
rs199558093	snp	A/G			missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151494163	CTCAAGACAATACCG[A/G]GCTAATGTTTTCTTG	4703
rs199558203	snp	A/G	6.10681e-05	0.00552542	intron-variant	NEB, RIF1	GRCh38.p7	2:151512683	AATGGAAGGACTTCC[A/G]TTCTTTCATGATTGG	4703
rs199564399	snp	C/T	0.000668419	0.0182692	intron-variant	NEB	GRCh38.p7	2:151642561	AGGCAAATAACTTTC[C/T]AAGTATACTTACTTC	4703
rs199584268	snp	C/T	0.000235789	0.0108554	missense, intron-variant	NEB	GRCh38.p7	2:151619740	TGACCCAACTGTTTA[C/T]GATATGCTTCTTTGT	4703
rs199594449	snp	C/T	0.000363985	0.0134855	missense	NEB	GRCh38.p7	2:151565117	AACGTATATTTGCCC[C/T]TTGCTTTATTAAATG	4703
rs199609054	in-del	-/TT			intron-variant	NEB	GRCh38.p7	2:151699179	ATCCATGTCCCTACA[-/TT]AAGGACATGAACTCA	4703
rs199639494	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151620652	AGGTTTTGTGAGTAG[A/C]TCAGCATACACACAT	4703
rs199650389	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151580540	ATTAAATCTCTTTAA[A/G]TACTTGTAAATTAAG	4703
rs199652902	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151495745	TTCATTTTTAAGTAA[A/G]TAAATTGATAATCAA	4703
rs199660489	snp	A/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151509366	AAAGAATAGAAACAA[A/T]CGTCCTTTTATTTTA	4703
rs199662534	snp	A/G	4.96792e-05	0.00498368	missense	NEB	GRCh38.p7	2:151666217	GATTTCTTTGCAGCT[A/G]TCACACTGACCATAT	4703
rs199665245	snp	C/T	9.17958e-05	0.00677418	intron-variant	NEB, RIF1	GRCh38.p7	2:151490534	CTGGGAGAGATGCAG[C/T]TGGGGGAGATGTAGC	4703
rs199673817	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151699727	TTGTTTTTTTCTTGT[A/C]AATTTGTTTGAGTTC	4703
rs199681309	snp	A/G	1.84181e-05	0.00303458	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151531835	GTACGCAGGTGTTCT[A/G]GAGTATCCACAATTG	4703
rs199683595	snp	C/G/T	8.32832e-05	0.00645256	missense, intron-variant	NEB	GRCh38.p7	2:151609879	ATGCATGTCCATTCA[C/G/T]GCAGGTAATTGCGAT	4703
rs199692784	snp	A/C/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151501132	CTTTTCTGGAAATCA[A/C/G]TTAACTTCAACAGTC	4703
rs199694315	snp	A/G	0.000861997	0.0207426	missense	NEB	GRCh38.p7	2:151663808	CATCTTCCAGGCTCC[A/G]GAAGCCAATGTGTTT	4703
rs199695976	snp	A/G	0.000780193	0.0197354	synonymous-codon	NEB	GRCh38.p7	2:151697595	GAATTTGGGGGTCTC[A/G]CAGTAATTTATGCTC	4703
rs199700878	snp	C/T	0.000910221	0.0213139	missense, intron-variant	NEB	GRCh38.p7	2:151654090	CTTCCCATCCAAGTT[C/T]ATAGAGTTTCTGAAA	4703
rs199702346	in-del	-/TCTG			intron-variant	NEB	GRCh38.p7	2:151690964	TTATATTCTCACTTC[-/TCTG]TCTGTCTCTCTCTCT	4703
rs199709120	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151664032	CTTCATTTTTTTTTT[C/T]CCCGAGACTTGAGTC	4703
rs199710125	snp	C/T	0.000199538	0.00998644	missense	NEB	GRCh38.p7	2:151696656	CTCAGTTGTTTGGAA[C/T]TGACTTGGGCTTGTA	4703
rs199722285	snp	G/T	1.68309e-05	0.00290089	missense	NEB	GRCh38.p7	2:151547678	CTTGGCGGATCTCAG[G/T]GGTATCGGGAGTTGT	4703
rs199722379	snp	A/G			missense, intron-variant	NEB	GRCh38.p7	2:151627653	TTCTTGGCTAACACC[A/G]CTCCCAGCATGTCCA	4703
rs199725501	snp	A/C/T	0.000666048	0.0182382	intron-variant	NEB	GRCh38.p7	2:151672320	AAAAGCGAGAAGTGA[A/C/T]CATCCTTTAAGTGCA	4703
rs199730497	snp	A/G	0.000645751	0.0179571	synonymous-codon	NEB	GRCh38.p7	2:151540383	CTTGGCTCTGATGAG[A/G]ATTGGCGTATCTGGA	4703
rs199738417	in-del	-/T	0.00449821	0.0472109	intron-variant	NEB	GRCh38.p7	2:151716143	TTCTTTTTTTTTTTC[-/T]TTTTTTCTCTTTTTG	4703
rs199738870	in-del	-/AAC	0.0360663	0.129354	intron-variant	NEB, RIF1	GRCh38.p7	2:151495666	ACAGTAAAACTAAAG[-/AAC]AACAACAACAACAAC	4703
rs199751776	in-del	-/TTTG	0.142947	0.22592	intron-variant	NEB	GRCh38.p7	2:151605973	ACGCCCAGCTAAGTT[-/TTTG]TTTGTTTGTTTGTTT	4703
rs199756204	snp	C/G	0.000123394	0.00785378	synonymous-codon	NEB	GRCh38.p7	2:151570554	GATGGCATCCAGCCG[C/G]ACATCACAGCCCGCC	4703
rs199766131	snp	C/T	1.65743e-05	0.00287869	missense	NEB	GRCh38.p7	2:151655859	GGCAAGCACCATGTC[C/T]ATGGAATCAGTCAGC	4703
rs199766288	snp	C/T	5.00329e-05	0.0050014	missense, intron-variant	NEB	GRCh38.p7	2:151612355	GGAACCCATCCTATG[C/T]CTCTCAGCCACTCAA	4703
rs199766446	snp	C/T	4.19666e-05	0.00458056	missense	NEB	GRCh38.p7	2:151687718	TGCTCTTCTCCCAGT[C/T]TTGCTTATAAACATT	4703
rs199770830	in-del	-/TGAG	0.0119091	0.0762411	intron-variant	NEB	GRCh38.p7	2:151574286	GCATGTTCTTACTCT[-/TGAG]TAATTATATTAGCAT	4703
rs199779426	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151647729	TCTTTACGAATGTCA[A/T]AAACTTGGAAGGCAA	4703
rs199786837	snp	G/T	8.33118e-05	0.0064536	intron-variant	NEB	GRCh38.p7	2:151540677	TTACCCAGTGCCTCA[G/T]TGCTGAATTCCCATC	4703
rs199789085	snp	C/T	0.000447335	0.0149488	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151618326	CTGCTCCGGAGTGTC[C/T]GTTATACTGGTAAAT	4703
rs199790903	in-del	-/A			intron-variant	NEB, RIF1	GRCh38.p7	2:151523888	TATGTATGTTTAATG[-/A]AAAAAAAAATGAATA	4703
rs199791504	snp	A/T	0.355811	0.226504	intron-variant	NEB	GRCh38.p7	2:151546002	TAGGTAATTAGACTT[A/T]AAAAAAAAAAAAAAA	4703
rs199793754	snp	A/G	0.000100588	0.00709113	intron-variant	NEB	GRCh38.p7	2:151670993	GTGTGGTTATTTACG[A/G]GCAAATCATTTTGAA	4703
rs199798402	snp	A/G			missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151525272	TTCTTTTTGTAATTT[A/G]TCTAAATAGAGCCAG	4703
rs199798472	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151590820	CCTTGGCCTCCCAAA[A/G]TGCTGGGATTACAGG	4703
rs199800122	snp	C/T	0.000422303	0.0145249	intron-variant	NEB	GRCh38.p7	2:151724214	ACATGAAATATATGA[C/T]GGGATGACATAGGAA	4703
rs199804593	snp	A/G	0.000834927	0.0204149	intron-variant	NEB	GRCh38.p7	2:151654110	AGTTTCTGAAAATTA[A/G]AGATATTCTTCAGCA	4703
rs199809548	snp	A/G	2.0166e-05	0.00317531	synonymous-codon	NEB	GRCh38.p7	2:151664777	ACTCATGGTGATTTG[A/G]TTTACTCTGGAGAGT	4703
rs199810746	in-del	-/C	0.0123036	0.0774623	intron-variant	NEB	GRCh38.p7	2:151656868	AAAAAGGCAAAAAAA[-/C]AGAACATTTCTCTTA	4703
rs199811860	snp	C/T	0.0103295	0.0711199	intron-variant	NEB	GRCh38.p7	2:151634514	GGGCGTGGTGGCGGG[C/T]GCCTGTAGTCCCAGC	4703
rs199822815	in-del	-/AACAT	0.0205511	0.0992634	intron-variant	NEB, RIF1	GRCh38.p7	2:151521406	AAAAGTTTCACTCTC[-/AACAT]AAAGAAGTGGAAGGC	4703
rs199822924	snp	A/T	0.00299544	0.0385843	missense	NEB	GRCh38.p7	2:151677955	TAATGATGGAGAGAA[A/T]GCTTATAGTTGACAT	4703
rs199835469	snp	C/T	3.31406e-05	0.00407053	synonymous-codon	NEB	GRCh38.p7	2:151554973	GCACCGTGCTGTGTT[C/T]GGATCATCGTCAACA	4703
rs199845420	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151577322	GTGTGTCCTGATCAC[A/C]CAGCCTGTCTTTCAA	4703
rs199847072	snp	A/T	0.000828089	0.0203312	missense, intron-variant	NEB	GRCh38.p7	2:151627148	TGACCACATCCATAG[A/T]CCCAATGGGGACCCA	4703
rs199859012	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151623688	AAAAATAAGAATCAA[C/T]TTAATATCTTTGAGA	4703
rs199862790	snp	A/G	0.00091092	0.0213221	missense	NEB	GRCh38.p7	2:151659120	TGGGGGATATCAGGC[A/G]TGATGTGGACTTTGG	4703
rs199868095	in-del	-/TTATT	0.0182019	0.0936463	intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151497278	TCAGAGTTATCCATG[-/TTATT]TTATTTTTTTTTTTC	4703
rs199870629	snp	A/G	4.97723e-05	0.00498835	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151627526	TTAATTACTCACATC[A/G]CTCTGGAGGTCATAG	4703
rs199875722	snp	C/G/T	0.0001331	0.00815688	missense	NEB	GRCh38.p7	2:151546364	AGCTTCCGCAGGTGC[C/G/T]GGGAGCGGACCATGT	4703
rs199883706	in-del	-/CC	0.0252325	0.109451	intron-variant	NEB	GRCh38.p7	2:151702417	TCAATTCCTTGATAT[-/CC]CCCTGTTGACTTTCT	4703
rs199886070	snp	A/G	0.00299544	0.0385843	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151603755	CTTCAGCCATTCCAG[A/G]TCTGACTTGTACAAG	4703
rs199890164	snp	C/G	9.93706e-05	0.00704808	missense, intron-variant	NEB	GRCh38.p7	2:151627788	TCAATGTTCCGGGCT[C/G]CAATGTGGTGGCCGA	4703
rs199890298	snp	C/T	0.00104371	0.0228203	missense	NEB	GRCh38.p7	2:151548337	TGTTGACTCTCCGGA[C/T]GTGGACAAATGGAAC	4703
rs199894970	snp	A/G	1.65696e-05	0.00287828	intron-variant	NEB	GRCh38.p7	2:151563727	TATTTAAGCTGTAAA[A/G]TGGGTTAAACATTGA	4703
rs199897201	snp	C/T	1.65608e-05	0.00287752	synonymous-codon	NEB	GRCh38.p7	2:151672543	GCTGGTTTTGGTGTT[C/T]TCATAGTTCTTCTTG	4703
rs199899629	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151694036	ATGTATATTAAGCTC[A/G]TTTCTAGGAAAAATA	4703
rs199903114	snp	G/T	0.000641482	0.0178978	missense	NEB	GRCh38.p7	2:151684842	TCAGGGGGGTAGCTG[G/T]AACTGTGTAAGATGT	4703
rs199907781	snp	C/T	0.000149176	0.00863514	missense	NEB	GRCh38.p7	2:151729632	CTCCCGGCACCTCTT[C/T]GTAAACCACTTCTTC	4703
rs199909877	snp	A/C	0.000116066	0.00761706	intron-variant	NEB	GRCh38.p7	2:151692187	AAATAAAACAAATGT[A/C]ATTCAAGTTAACAAT	4703
rs199920828	snp	A/C/G	5.70467e-05	0.00534042	missense	NEB	GRCh38.p7	2:151724277	TGCTGAACATGGCGG[A/C/G]GTTCTTAACGGCCTG	4703
rs199934793	snp	A/T	8.29098e-05	0.00643801	missense, intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151534284	TACCAGGTGGTATTT[A/T]TCTTTCCGCTGCTCA	4703
rs199937246	snp	C/T	0.000980692	0.022122	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151494220	GAGTGACAGGGGTTG[C/T]GGTGGCTTTCCCCAC	4703
rs199952912	in-del	-/TA	0.0154538	0.0865337	intron-variant	NEB	GRCh38.p7	2:151687030	GAACGATACTCTATT[-/TA]AAGATTTTTGTGACT	4703
rs199957886	snp	G/T	0.000325549	0.0127542	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151508079	TCTCATAATACGACA[G/T]GGACTTCTCAGCATC	4703
rs199966292	in-del	-/A	0.040671	0.13668	intron-variant	NEB	GRCh38.p7	2:151659601	CACTGCACCTGGCCC[-/A]AAAAAAATTTTAATG	4703
rs199967751	in-del	-/G			intron-variant	NEB	GRCh38.p7	2:151669689	TAGACAGAAGGTGCA[-/G]AAGGGCCACAGAGAA	4703
rs199969138	snp	A/G	0.000932952	0.0215779	synonymous-codon	NEB	GRCh38.p7	2:151709707	ATACTCTGGTGTTTC[A/G]GTCTGCATGAAGTAG	4703
rs199974460	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151707009	TTACCTGTAGGAGTG[A/C]AATAAAATGATAAAG	4703
rs199977733	snp	C/T	8.28809e-05	0.00643689	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151650290	CTCACTGATGATTTC[C/T]GAAGCCCGCTTGTTC	4703
rs199990202	snp	C/T			intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151497293	GTTATTTTTTTTTTT[C/T]CTTTTTTGTGAGTAC	4703
rs200002537	snp	C/T	0.000116989	0.00764729	missense	NEB	GRCh38.p7	2:151671187	CAATAGGGATCCATC[C/T]GATGCCCTTCAAGAA	4703
rs200006992	in-del	-/A			intron-variant	NEB	GRCh38.p7	2:151629073	TTAAGATAATTTTCC[-/A]AAAAAAAAATGAGTT	4703
rs200011828	snp	C/T	2.27265e-05	0.00337087	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151526252	TTGACATGTTTCTCT[C/T]TGTATTTCAGCTTCA	4703
rs200015472	snp	C/T			missense, intron-variant	NEB	GRCh38.p7	2:151644101	ATGTGGTGGCCGAGC[C/T]GCTTGCGAAAGCCTT	4703
rs200018782	snp	A/C/G	0.00150733	0.0274134	synonymous-codon	NEB	GRCh38.p7	2:151655904	GTTGCTCGGGTGCTG[A/C/G]CGGTATTTCTGATCA	4703
rs200022613	in-del	-/A			intron-variant	NEB	GRCh38.p7	2:151615704	CTCAATTATTTATTT[-/A]TTTTTTTTGAAGACG	4703
rs200043736	snp	C/T	3.31329e-05	0.00407005	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151614516	GGACCACATCATCTT[C/T]GGGTCATCCTTAATG	4703
rs200050128	snp	A/G	2.45921e-05	0.00350648	missense	NEB	GRCh38.p7	2:151665517	CCTTTCATCCAATTG[A/G]TGAAGTCAGATTTGT	4703
rs200053313	snp	G/T	0.222678	0.248502	missense, intron-variant	NEB	GRCh38.p7	2:151590049	ACAGGGATGGAGATC[G/T]TGGCTTTGTGGTCGT	4703
rs200056050	snp	C/T	3.50275e-05	0.0041848	missense	NEB	GRCh38.p7	2:151561053	TCATAATCCACTGTT[C/T]CTAGAACTGTTGTGT	4703
rs200057961	snp	C/T			missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151493785	AATACCGAGCTAAAG[C/T]TTTCTTGATTGCGTT	4703
rs200059745	snp	A/C/T	0.000412482	0.0143554	intron-variant	NEB	GRCh38.p7	2:151679698	TTTTCTAGTTGCCCA[A/C/T]GTATGACCACAGCTG	4703
rs200059848	snp	C/T	3.31301e-05	0.00406989	intron-variant	NEB	GRCh38.p7	2:151575692	GTCTGTTGTAGTACT[C/T]ACATTGCTCACATTA	4703
rs200067860	snp	A/G	0.4973	0.0366419	intron-variant	NEB	GRCh38.p7	2:151608798	ATCCCAGCTACTTGG[A/G]AGGCTGAGGCAGGAG	4703
rs200079863	snp	A/T			intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151499039	AAAGCAGTATAAATG[A/T]GGATGCTTAGACACT	4703
rs200083849	snp	C/T	0.000115931	0.00761264	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151490007	TGGGATGGAAGATAC[C/T]GTTGTCTGTTGGGTA	4703
rs200090059	snp	C/T	0.00299557	0.0385851	splice-donor-variant	NEB	GRCh38.p7	2:151568315	TGGGTGAAACCCATA[C/T]CTGGTCCAGTATCCT	4703
rs200091194	snp	A/G	4.06314e-05	0.00450711	intron-variant	NEB	GRCh38.p7	2:151642916	GGCCAGTAATAAATA[A/G]ACACATGCAGACAGT	4703
rs200104698	snp	A/G	0.000120655	0.00776615	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151531040	TGCAGCAACATGGGT[A/G]TGTCGTGGATTGTGG	4703
rs200112795	snp	A/G/T	0.00201094	0.0316453	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151531895	TTTTTCCTGTATTTG[A/G/T]TCTAAATTGTGGAAG	4703
rs200113036	snp	C/T	0.00144098	0.0268032	intron-variant	NEB, RIF1	GRCh38.p7	2:151514295	TGTATGAATTACGTG[C/T]AGGCAGTCAGCTGTG	4703
rs200122580	snp	A/G	0.000270464	0.0116258	synonymous-codon	NEB	GRCh38.p7	2:151562632	CAAGATCTCCTGGGC[A/G]TTTCGGACGCGTATA	4703
rs200125713	snp	G/T	0.230622	0.249248	missense, intron-variant	NEB	GRCh38.p7	2:151600602	ACAGGGATGGAGATC[G/T]TGGCTTTGTGGTCGT	4703
rs200145194	snp	C/T	0.300421	0.244863	intron-variant	NEB	GRCh38.p7	2:151605341	ATCTCCATCACCAAG[C/T]TTCCCTGACAAGTGC	4703
rs200146776	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151608439	GGCTCAGTTTGGGTG[C/G]TATCTTTGGAAAAGA	4703
rs200151543	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151727070	AAAAAAAAAAAAAAA[A/C]CCTTTCTGCACAGTC	4703
rs200154617	snp	C/T			missense	NEB	GRCh38.p7	2:151725517	TCTGTTGTGCTGGCG[C/T]ATGGCTGTCCTTTTG	4703
rs200165006	snp	A/G	8.44744e-05	0.00649847	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151492419	GGGTCTCCCTCACCC[A/G]TCTCATCTCGGGGGT	4703
rs200165275	in-del	-/ACA			intron-variant	NEB, RIF1	GRCh38.p7	2:151512881	ATGTTTGCAATGTGC[-/ACA]ACAACAGTTGTTGGC	4703
rs200179236	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151692375	TCTCTGTTAAAGGAA[A/G]AATAAATTAAACCAA	4703
rs200193449	in-del	-/AA	0.0221141	0.102801	intron-variant	NEB, RIF1	GRCh38.p7	2:151487744	ATGGCATGTGTGTTT[-/AA]ACTTATTTTATACAT	4703
rs200195063	snp	C/T	0.00028073	0.0118442	missense	NEB	GRCh38.p7	2:151562642	TGGGCGTTTCGGACG[C/T]GTATAACATTGGGTT	4703
rs200200798	in-del	-/CTT	0.02016	0.0983543	intron-variant	NEB	GRCh38.p7	2:151573903	TAAGACTTAAAATGA[-/CTT]CTTCTGCAAATAATG	4703
rs200201736	snp	C/T	0.0209421	0.100162	intron-variant	NEB	GRCh38.p7	2:151579253	AAAGTGGAGTGCCTA[C/T]GTACAGAGAGTTGTG	4703
rs200207568	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151669774	CCTAAGAGGTTTTAC[A/T]CATAAGAGGGACATG	4703
rs200221888	in-del	-/C	0.0912534	0.193131	intron-variant	NEB, RIF1	GRCh38.p7	2:151502209	ACAGTGAACTTTGGG[-/C]GACTTGCAGGAAAGA	4703
rs200231116	in-del	-/T	0.00478085	0.0486577	intron-variant	NEB	GRCh38.p7	2:151625374	CTTTCTATCTGCCTA[-/T]TTTTTAATACAATAA	4703
rs200239095	snp	A/G	0.00270332	0.0366654	missense	NEB	GRCh38.p7	2:151549653	AACTGCTCATGTAAC[A/G]GGTGTCCTTGATGTG	4703
rs200246050	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151729991	AGAATTTGCTGAGAA[G/T]AGAATACAATAAGAA	4703
rs200247246	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151605534	AGAGTTTCCATCTGA[C/T]GAGTGTCTCAGGACT	4703
rs200250294	snp	C/T	0.000350712	0.0132376	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151527542	CGGTCAGGAGTCCAC[C/T]TCCAGTGGGCTTTGT	4703
rs200251444	snp	A/G	0.000577185	0.0169782	missense	NEB	GRCh38.p7	2:151658078	ACTCTTCCAAGGAAA[A/G]TTTGTAGAGTTTCTG	4703
rs200261335	snp	C/G	8.40371e-05	0.00648163	intron-variant	NEB	GRCh38.p7	2:151540309	AACCTCAGCTCTCCC[C/G]ATCACAACAGAAGAA	4703
rs200263587	snp	A/G	0.000780092	0.0197342	intron-variant	NEB	GRCh38.p7	2:151668992	AGAAAGGAGAGGCCC[A/G]CATACGCAATATTAG	4703
rs200269437	snp	A/G	0.000185856	0.00963813	missense, intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151499371	GGAATCCCTTTTCCA[A/G]CGTTTTCTTTATACA	4703
rs200270156	snp	A/G	0.00018225	0.00954421	missense, intron-variant	NEB	GRCh38.p7	2:151614544	ATGTTCCGGGCCCCA[A/G]TATGGTGGCCAAGCT	4703
rs200289181	snp	A/C/T	3.34466e-05	0.0040893	intron-variant	NEB	GRCh38.p7	2:151687381	ATCGTAACAGGGAGT[A/C/T]CATCTTGAAAACAAG	4703
rs200293825	snp	A/G	6.62515e-05	0.00575512	intron-variant	NEB, RIF1	GRCh38.p7	2:151518302	CCAGAGGAAAAATCG[A/G]TCTTGATCCACTTAC	4703
rs200297299	snp	A/T	0.00295362	0.0383156	synonymous-codon	NEB	GRCh38.p7	2:151727817	TGCTGGCTGTGCCAG[A/T]GCTGGCTGTGCCAGA	4703
rs200298261	snp	C/T	0.000480638	0.0154948	missense	NEB	GRCh38.p7	2:151697457	AATCTTTATATTTTT[C/T]CTGCAAGACAAAACA	4703
rs200304547	snp	C/G	0.000314609	0.0125382	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151526011	TGTCCCGGGTCTCTG[C/G]TAGTGTTGTGTATGA	4703
rs200307392	snp	C/T	0.00109338	0.0233559	missense, intron-variant	NEB	GRCh38.p7	2:151639945	CTGTCTGGAGGCTGG[C/T]GATAGATTTTATCAC	4703
rs200323882	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151699009	TATCTCCCAATGCTA[C/T]CCCTCCCCCCTCCCC	4703
rs200333206	snp	A/G	0.000347783	0.0131822	synonymous-codon	NEB	GRCh38.p7	2:151553972	CATCTCTACCATGTC[A/G]GGCACGATGTGGATT	4703
rs200335438	snp	A/G	1.65666e-05	0.00287802	synonymous-codon	NEB	GRCh38.p7	2:151576277	ATTCTGGGCGTTTTT[A/G]ACTCTCAACACTTCA	4703
rs200350243	snp	C/T	5.38121e-05	0.00518683	intron-variant	NEB	GRCh38.p7	2:151551709	TGGAACGGATTTCTG[C/T]TGGGCACTCTCAAGT	4703
rs200351671	snp	A/G/T	0.000168344	0.00917324	missense, intron-variant	NEB	GRCh38.p7	2:151630819	CCTCTGTGTATAAAC[A/G/T]CTATAAAAGAAGATA	4703
rs200384957	in-del	-/CAT	0.0119091	0.0762411	intron-variant	NEB, RIF1	GRCh38.p7	2:151494511	AGGATGAGAAACCAC[-/CAT]CATCATTTTACCGCT	4703
rs200386897	snp	C/T	0.000430478	0.0146647	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151640415	CTGGTCGGGCAGGCA[C/T]GTCCACTGGTGCAGG	4703
rs200393215	snp	C/T			missense, intron-variant	NEB	GRCh38.p7	2:151629606	CTTCGCAAGTCGTAG[C/T]CTTTCTTTTTTGCTT	4703
rs200412065	snp	C/T	0.000382314	0.0138207	missense	NEB	GRCh38.p7	2:151664539	CTCTTGCAGCCTTTA[C/T]TGCAATGGCATCAGG	4703
rs200425929	snp	A/G	0.00129133	0.0253771	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151644531	ATCAACAGGAAGATC[A/G]TAACCTTTTCTCTTC	4703
rs200427401	snp	A/G	0.000994728	0.0222795	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151618284	ACTCACCTTATTCAT[A/G]TTTAAAGCATTGTTT	4703
rs200433466	in-del	-/TC			intron-variant	NEB	GRCh38.p7	2:151638798	ACACTGACAGATATT[-/TC]TCTCTCTCTGTGTGT	4703
rs200433731	snp	C/T	0.000718529	0.0189406	intron-variant	NEB	GRCh38.p7	2:151725424	TATTTTGAAATGTCC[C/T]TCTCCTTTATTTCAG	4703
rs200436252	snp	A/G	7.26296e-05	0.00602574	intron-variant	NEB	GRCh38.p7	2:151669001	AGGCCCGCATACGCA[A/G]TATTAGCACTGGGCC	4703
rs200449517	snp	A/G	0.000232605	0.0107818	splice-donor-variant, intron-variant	NEB, RIF1	GRCh38.p7	2:151519656	CAATTTTAGAAACAT[A/G]CCTCACTTGCAAGAT	4703
rs200454939	snp	A/G	3.3389e-05	0.00408575	missense, nc-transcript-variant, intron-variant	NEB, RIF1	GRCh38.p7	2:151506910	AATAGTAAATATACC[A/G]AGCTGAAATTCTTCT	4703
rs200462172	snp	A/C	0.000399281	0.0141238	missense	NEB	GRCh38.p7	2:151672606	CATATAGTGGACCAG[A/C]TTGGGATCATCCTGG	4703
rs200462308	snp	A/C/G	0.000240816	0.0109706	missense, intron-variant	NEB	GRCh38.p7	2:151625638	CTTCTGTGTATAAGC[A/C/G]CTGTGAAGGATAAAA	4703
rs200468391	snp	G/T	0.000398274	0.014106	missense	NEB	GRCh38.p7	2:151663746	CTTCTTGTATTCCCG[G/T]TCTGACTGCATCTTG	4703
rs200473774	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151668364	TAATTGATCTTAATG[C/T]TTAAATATTACTTAG	4703
rs200479578	snp	C/T	0.000414096	0.0143832	intron-variant	NEB	GRCh38.p7	2:151575662	TGACTGGGTAACTTT[C/T]CAAACAAAAAGAGAG	4703
rs200481156	snp	C/T	4.97211e-05	0.00498579	missense	NEB	GRCh38.p7	2:151655861	CAAGCACCATGTCCA[C/T]GGAATCAGTCAGCTT	4703
rs200482878	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151608441	CTCAGTTTGGGTGGT[A/T]TCTTTGGAAAAGATA	4703
rs200484073	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151494122	ACTGCAAGAGTTATT[C/T]TGCAAAATTAAAAGC	4703
rs200486452	snp	C/T	0.00299551	0.0385848	missense, intron-variant	NEB	GRCh38.p7	2:151646189	GTGTATCAGGCATGA[C/T]GTGGATCTGAGTCTT	4703
rs200486767	snp	C/T	0.000118064	0.00768231	missense	NEB	GRCh38.p7	2:151684972	AATCTTTTCGATATT[C/T]GCGCTGTGAATAGGA	4703
rs200488898	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151559106	CAAGAAAAAAACAAA[A/C]AACCCCATCAAAAAG	4703
rs200489965	snp	C/G	1.66263e-05	0.00288321	synonymous-codon	NEB	GRCh38.p7	2:151696658	CAGTTGTTTGGAATT[C/G]ACTTGGGCTTGTAGC	4703
rs200492532	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151605502	ATCAGAAGATAACAA[C/T]AAAAGTTCTGTGGAC	4703
rs200496403	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151578586	GAATCGCTTGAACCC[A/G]GGAGGCAGAGGTTGC	4703
rs200501968	snp	C/T	3.70686e-05	0.00430499	missense	NEB	GRCh38.p7	2:151570382	TTCTCATGGTCAAGC[C/T]TATATTTATACTGGA	4703
rs200521644	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151546796	ACTCCTGACCTCAGG[C/T]GATCTGCCCACCTCA	4703
rs200523155	snp	A/G	0.000267098	0.0115533	missense	NEB	GRCh38.p7	2:151537166	TTCTTTTCAGCCAGA[A/G]TGAAATCAGGGGTAT	4703
rs200531108	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151591331	GTTTGTTCCGGTTGG[C/G]AAGGAGGAGCTCTTA	4703
rs200532658	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151495447	CCTGCACGTTATTCT[A/G]ATGCGTGCTAATGTT	4703
rs200540053	in-del	-/G			intron-variant	NEB	GRCh38.p7	2:151561484	CTGCCAGAATGAATA[-/G]CTTCTCTTGACTGAG	4703
rs200544122	snp	C/T			missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151494171	AATACCGAGCTAATG[C/T]TTTCTTGATTGCGTT	4703
rs200545007	snp	A/G/T	0.00109252	0.023347	NEB	2	allele_origin=G(germline)/A(somatic)	2:151666287	CCTTTTTGTACTCAC[A/G/T]ATCAGACTGGATTTT	4703
rs200548050	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151652538	CCTCCAAAATTCTTA[C/T]ATTTTTAAGTATCTA	4703
rs200555425	snp	A/G	0.000132527	0.00813916	missense	NEB	GRCh38.p7	2:151725488	CTTTTTTGATTCTGC[A/G]AAGTTCTGGAGTATC	4703
rs200557002	snp	A/G	3.3134e-05	0.00407012	missense, intron-variant	NEB	GRCh38.p7	2:151614517	GACCACATCATCTTC[A/G]GGTCATCCTTAATGT	4703
rs200559481	snp	A/C	0.000201349	0.0100316	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151502881	AAATTTTCTTTGTAC[A/C]AAACCTGTGAGATAC	4703
rs200564629	snp	C/G/T	1.65685e-05	0.00287819	missense	NEB	GRCh38.p7	2:151679929	GCACCTCACTGATAT[C/G/T]GTAGGCATTAACTTT	4703
rs200579863	snp	A/T	0.00299551	0.0385848	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151501413	AAGTTTTCTTGATTG[A/T]GTTTGACTCGCTCCA	4703
rs200580792	in-del	-/T	0.0509478	0.151255	intron-variant	NEB	GRCh38.p7	2:151708184	CTTTCTACTGGATTC[-/T]TTCCATCAACATGAT	4703
rs200580970	snp	C/G	0.041118	0.137362	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151590051	AGGGATGGAGATCTT[C/G]GCTTTGTGGTCGTTG	4703
rs200583505	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151699993	AGGGTTTTTATGGTT[G/T]TAGGTCTAACGTTTA	4703
rs200585609	snp	A/G	0.000149401	0.00864166	missense	NEB	GRCh38.p7	2:151697590	AGCTTGAATTTGGGG[A/G]TCTCGCAGTAATTTA	4703
rs200590080	snp	A/G/T	0.000200114	0.0100011	missense, synonymous-codon	NEB	GRCh38.p7	2:151724938	TATAGTCTTAGCAAC[A/G/T]TCACCATCCATTCGA	4703
rs200591649	snp	C/G	1.65715e-05	0.00287845	missense, intron-variant	NEB	GRCh38.p7	2:151610620	ATCCCTTGGTGTAAA[C/G]TTTCTAGGGAAGGGA	4703
rs200602229	snp	C/G	0.1609	0.233583	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151579500	AGGGATGGAGATCTT[C/G]GCTTTGTGGTCGTTG	4703
rs200624735	snp	C/T	0.000595977	0.0172521	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151640487	CTTGGCCAGCACCAC[C/T]CCCAGCATGTCCACT	4703
rs200637566	snp	A/G/T	0.000696262	0.0186466	missense	NEB	GRCh38.p7	2:151678000	TGGGCTTTCTTAGCC[A/G/T]CCACGACATTGAACA	4703
rs200649387	snp	C/T	1.65792e-05	0.00287912	missense	NEB	GRCh38.p7	2:151662251	CACTAATAATCTCCA[C/T]GGCTTTCTTGTTTTT	4703
rs200658908	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151580621	AGAGTTGCAGAACCA[A/G]ACATAGATGCAAAAG	4703
rs200661161	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151671986	CTTGAGTTAATAAAG[A/G]AAAAAAAAAAACACC	4703
rs200662106	snp	A/C	0.000742868	0.0192583	intron-variant	NEB	GRCh38.p7	2:151567151	TTCTAGATAATGAAG[A/C]AACAAAAATCACTTA	4703
rs200662950	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151608135	ACACACACACACACA[C/G]AGCCCCTATTGGTTC	4703
rs200664249	in-del	-/C	0.0166325	0.0896639	intron-variant	NEB	GRCh38.p7	2:151575304	TGATTTTCTAGAAAA[-/C]CCCCCCGAGGTCCAT	4703
rs200664592	snp	A/C	0.000798403	0.0199641	missense	NEB	GRCh38.p7	2:151687690	TCCACTTTAATGTCA[A/C]ACTTCTTGGCTTTGC	4703
rs200672688	snp	A/C/G	3.31726e-05	0.00407252	missense	NEB	GRCh38.p7	2:151710484	CAACTTCAAAGCAAG[A/C/G]TGTCTCACTCCATTT	4703
rs200672818	snp	C/T	0.000101451	0.00712145	missense	NEB	GRCh38.p7	2:151570296	CATTCTGGAGCTTGT[C/T]AGCTATGAGGGCCCA	4703
rs200698871	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151722917	GACACACCACAATTT[A/G]GACTTGATGATTAGA	4703
rs200703673	snp	A/G	0.00387417	0.0438415	missense, intron-variant	NEB	GRCh38.p7	2:151579372	GCTTTCCTGGCTTGG[A/G]TCACATCATTCTGGT	4703
rs200719359	snp	C/T	0.00306272	0.0390126	missense	NEB	GRCh38.p7	2:151724333	AGCAGGTACTTATCC[C/T]TGGTGTCTTCCCAGT	4703
rs200721646	snp	G/T	0.00299551	0.0385848	intron-variant	NEB	GRCh38.p7	2:151659016	AATTTGTTCTTACTG[G/T]TTCAAATCTGCTGGA	4703
rs200729207	snp	C/T	0.000711973	0.0188542	missense, intron-variant	NEB	GRCh38.p7	2:151640396	GAGCATGGATGACGT[C/T]GCTCTGGTCGGGCAG	4703
rs200731507	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151650023	TTCAGTGTAGGATAG[C/T]TGCTAATTCAAATAA	4703
rs200731870	snp	A/G	0.000115958	0.00761352	stop-gained, intron-variant	NEB, RIF1	GRCh38.p7	2:151490039	CAACTGAAGATGATC[A/G]TTGTTGTGGGAGCTC	4703
rs200743562	snp	A/G	1.65611e-05	0.00287755	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151614453	GGTCTTCCACTTCTC[A/G]AACTCCTTCTTGTAC	4703
rs200744202	snp	A/G	5.92575e-05	0.00544291	intron-variant	NEB	GRCh38.p7	2:151664901	ATGATTTTACAGCAG[A/G]ACAAGTTTGACCCAA	4703
rs200758495	snp	A/G	0.000419045	0.0144688	synonymous-codon	NEB	GRCh38.p7	2:151696637	GTTAGAGGAACTTAC[A/G]TCACTCAGTTGTTTG	4703
rs200761405	snp	C/T	0.000356189	0.0133404	missense, intron-variant, utr-variant-3-prime	NEB, RIF1	GRCh38.p7	2:151497651	TTTTCTTGATTGTGT[C/T]TGACTCTTTCCATCT	4703
rs200776925	snp	C/G	0.000696067	0.0186427	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151519700	CATGACTTTGTAGAG[C/G]TGGCTGTCTTTTGGA	4703
rs200783124	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151559040	TTCTGCAATCTATCC[A/G]TCTGACAATGGGCTA	4703
rs200783974	snp	A/G	0.0029955	0.0385847	missense	NEB	GRCh38.p7	2:151679762	TGGCAGCTCTGATGG[A/G]AATCGCATCAGTTCT	4703
rs200790107	in-del	-/C	0.0337553	0.125452	intron-variant	NEB, RIF1	GRCh38.p7	2:151523859	ATCCCTACTTCCTAG[-/C]CCGGGCAGTTAATAT	4703
rs200792421	snp	C/G	0.000116101	0.00761819	synonymous-codon, intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151534245	GCCTGCGGTCTTAGC[C/G]AGCAGATGTCTAGGC	4703
rs200793308	in-del	-/AACT	0.0807149	0.183963	intron-variant	NEB	GRCh38.p7	2:151592278	TTTATAATAAATTAA[-/AACT]AACATAAGTAAATTA	4703
rs200804762	snp	A/G	5.12904e-05	0.00506385	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151492401	CCGTTGAGATGTGCC[A/G]TTGGGTCTCCCTCAC	4703
rs200811504	in-del	-/G			intron-variant	NEB	GRCh38.p7	2:151722473	AAGTATCTTCTGATA[-/G]GCAAGAGCTCTTTGT	4703
rs200813844	snp	C/T	1.7842e-05	0.00298675	missense	NEB	GRCh38.p7	2:151656160	AGCCTTACATCACTC[C/T]GTATGCGATTCATAT	4703
rs200819489	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151520944	CCTAATTGAAAAACA[A/G]ACTGATGCTTTTGTC	4703
rs200822815	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151638807	GATATTTCTCTCTCT[C/G]TGTGTGTGTGTGTGT	4703
rs200826420	snp	A/G	8.89197e-05	0.00666723	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151531020	CATCTTTAACCTTGC[A/G]GACATGCAGCAACAT	4703
rs200830455	in-del	-/TATATATATATTTTTTTTTTTTTTT			intron-variant	NEB	GRCh38.p7	2:151576507	ATATATATATATATA[-/TATATATATATTTTTTTTTTTTTTT]TTTTTTTTTTTTTTT	4703
rs200831033	snp	A/G	0.000272072	0.0116603	intron-variant	NEB	GRCh38.p7	2:151576402	TGTGTTTTGTTGTGT[A/G]TGTGTGTGGTAAAAT	4703
rs200832059	in-del	-/TAA			intron-variant	NEB, RIF1	GRCh38.p7	2:151525656	AATTGGGTAGCAGTT[-/TAA]TAATAATAGGAGAGG	4703
rs200889451	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151546803	ACCTCAGGTGATCTG[C/T]CCACCTCAGCCTCCC	4703
rs200898845	in-del	-/CA	0.0221141	0.102801	intron-variant	NEB, RIF1	GRCh38.p7	2:151517588	TCATTGTGTGAACAT[-/CA]CAGAGTACACTTACA	4703
rs200899978	snp	G/T	0.178465	0.239547	intron-variant	NEB	GRCh38.p7	2:151675776	AGAGAAAGTAGTAGT[G/T]AGAATAAGTTTTTCA	4703
rs200902944	snp	A/G	0.000760913	0.0194904	intron-variant	NEB, RIF1	GRCh38.p7	2:151492289	TATTTCACCTGAAAT[A/G]TCATGAATTTGCTTT	4703
rs200914547	snp	A/C	0.0039921	0.0444985	intron-variant	NEB	GRCh38.p7	2:151551730	ACTCTCAAGTTCTCA[A/C]TGCTCACCGAACTCT	4703
rs200914626	snp	C/T	0.000391183	0.0139799	synonymous-codon	NEB	GRCh38.p7	2:151706914	TGCTGCCTTCAGCTG[C/T]CTAAGCTGTGGGTTC	4703
rs200915116	snp	C/T			missense	NEB	GRCh38.p7	2:151697623	CTCTTTGCTTTTGTC[C/T]TTTCATAGTTTTCCT	4703
rs200915591	snp	C/T	0.00177212	0.029714	intron-variant	NEB	GRCh38.p7	2:151626984	CCTGTCTTATTTTCC[C/T]ACAAATTGGGGGCTC	4703
rs200915868	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151701178	acatttattgatttg[C/T]gtatattgaaccagc	4703
rs200918570	snp	C/T			missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151526166	GGGTTACCTCAGACA[C/T]CAGGTTGCTGACAGT	4703
rs200930670	snp	A/C/T	9.93845e-05	0.00704865	missense, intron-variant	NEB	GRCh38.p7	2:151629594	GGGATGGCGTCACTT[A/C/T]GCAAGTCGTAGCCTT	4703
rs200936927	snp	A/C/G/T	4.98661e-05	0.00499309	synonymous-codon	NEB	GRCh38.p7	2:151727736	GTGTGCAATGTAGGG[A/C/G/T]GTCATGAACTTTGAA	4703
rs200945025	snp	C/T	0.00173182	0.0293753	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151527483	TCTCCTGTCTTACAT[C/T]GCTTTGCTGCAGGGA	4703
rs200950755	snp	A/G	0.00299544	0.0385843	intron-variant	NEB	GRCh38.p7	2:151724795	CAATTTTCTCCTATA[A/G]GACAATGCAGAGGTG	4703
rs200951652	snp	C/T	3.68942e-05	0.00429485	missense	NEB	GRCh38.p7	2:151694527	CCACACTCACATCGC[C/T]GGTGTTCTTGGTGTT	4703
rs200952733	snp	A/G	0.00011602	0.00761554	missense	NEB	GRCh38.p7	2:151576236	AGGTTCACCACAGGC[A/G]TCCGATAGACACTGT	4703
rs200954059	snp	A/G	0.000399281	0.0141238	synonymous-codon	NEB	GRCh38.p7	2:151656189	ATTCCTGGTCAGCTC[A/G]ATGTTCATTGCATCT	4703
rs200963111	snp	C/T	0.00049699	0.0157559	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151513680	TCCAGTTCCAGGTCT[C/T]GCTTATATTCTTTCT	4703
rs200970764	snp	C/G	0.00299551	0.0385848	intron-variant	NEB	GRCh38.p7	2:151646078	AATTTCACTGATTTA[C/G]AAACAATTAAAATGA	4703
rs200979504	snp	C/T			missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151502825	GATTGCGTTTGACTC[C/T]CTCCATCTCTGGAGT	4703
rs200983285	in-del	-/TAATCTGCC			intron-variant	NEB, RIF1	GRCh38.p7	2:151530056	TGTTATAATTTTTTT[-/TAATCTGCC]TATTCTTTCCATTAA	4703
rs200985915	snp	A/G	0.00299544	0.0385843	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151609937	ATTTCTTGGCCAGCA[A/G]GATGCTTAACATGTC	4703
rs200990309	snp	C/T	0.00152614	0.0275815	synonymous-codon	NEB	GRCh38.p7	2:151727808	CTTTGCTGATGCTGG[C/T]TGTGCCAGTGCTGGC	4703
rs200998609	in-del	-/GGA			intron-variant	NEB	GRCh38.p7	2:151717385	AGCAGAGTCTTCAAG[-/GGA]GGAGGCAATGTCCCA	4703
rs201001168	snp	C/T	5.49466e-05	0.00524121	missense	NEB	GRCh38.p7	2:151545961	ACTTTGTATTTGTCT[C/T]GCATCTTCCTTGCCT	4703
rs201005449	snp	A/G/T	0.000257288	0.0113394	missense, synonymous-codon	NEB	GRCh38.p7	2:151560622	CTTCTGGTTCTTGGC[A/G/T]TGTGTCAGGGACAAG	4703
rs201008053	snp	G/T	0.084728	0.187577	intron-variant	NEB	GRCh38.p7	2:151594831	AATGATCTCCTAAGA[G/T]TACTGAAGGAACCTC	4703
rs201020210	in-del	-/A			intron-variant	NEB	GRCh38.p7	2:151624729	CCTTCCTTTTTCTCT[-/A]AAAAAAAAATGAAGA	4703
rs201022605	snp	A/G	1.73123e-05	0.00294208	intron-variant	NEB, RIF1	GRCh38.p7	2:151492353	TACACATTCTGACAG[A/G]CAGCCAGCCAATCCT	4703
rs201028196	snp	C/G	0.000398439	0.0141089	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151503421	TGGAATGCCTGTTCC[C/G]AAGTTTTCTTTGTAC	4703
rs201046240	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151603531	TCTGGATTCAGATTT[A/C]TTCCATTTGTCTGAA	4703
rs201046639	in-del	-/AC	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151559952	ATAAACCAAAACAAA[-/AC]ACACACACACGCAAA	4703
rs201057354	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151677458	AATAAACAAAATAAT[A/T]TAAAATGGAAAGATA	4703
rs201065426	snp	C/T	1.66369e-05	0.00288412	missense	NEB	GRCh38.p7	2:151692310	TATTTTGGGGTCTCA[C/T]AGTAATTCATACTCT	4703
rs201071685	snp	C/T	0.00253317	0.0354989	missense	NEB	GRCh38.p7	2:151548376	GGCCAAGTGTATACC[C/T]ATATGCCTTGGTGTG	4703
rs201072996	snp	A/G	0.000877592	0.0209291	missense	NEB	GRCh38.p7	2:151568371	AGGGGGGTTTCTGTG[A/G]GGGTGTACTTTGATT	4703
rs201080620	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151627357	TACAGTCTCAGGTAT[C/T]ACTTTCTTTCTCTCC	4703
rs201082106	snp	A/G	0.00299544	0.0385843	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151505530	ACTTCAGGCAGGTCA[A/G]GGATTGGAGTTCCTT	4703
rs201094376	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151546770	CACCATGTTGGCCAG[G/T]CTGGTCTCGAACTCC	4703
rs201094791	snp	C/T	0.000904159	0.0212429	intron-variant, missense	NEB, RIF1	GRCh38.p7	2:151533488	GTCAACATATCTGGA[C/T]GCAGAATTTCATTAC	4703
rs201111610	snp	C/T			missense, intron-variant	NEB	GRCh38.p7	2:151579405	GGAAAGCAAGACCAG[C/T]GGTGCAGGTAATGGC	4703
rs201119402	snp	C/T	0.000844322	0.0205292	missense, intron-variant	NEB	GRCh38.p7	2:151643247	TGCTGACGGTAAACA[C/T]GGTCACTCAAAATCT	4703
rs201121053	snp	A/T	2.55647e-05	0.00357515	intron-variant	NEB	GRCh38.p7	2:151562579	AGTCATGGAAGCTGT[A/T]GCTGAGTCAAGCTGC	4703
rs201121298	snp	A/C	1.76708e-05	0.00297239	intron-variant	NEB	GRCh38.p7	2:151650147	GGTAGCAGGCACTAT[A/C]ATCTATTTATTTCCA	4703
rs201124975	snp	C/G	0.000124979	0.00790404	missense	NEB	GRCh38.p7	2:151684833	TTGATGCTATCAGGG[C/G]GGTAGCTGTAACTGT	4703
rs201126336	snp	A/C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151565452	CCACCCAATGATAGA[A/C/T]AATTTACTCCCCAGT	4703
rs201132539	snp	A/G	1.74888e-05	0.00295704	missense, intron-variant	NEB	GRCh38.p7	2:151650608	ACTTTCTTAGCTTGC[A/G]CAACATCGTTCTGAT	4703
rs201141958	snp	A/G	0.00248106	0.0351336	missense	NEB	GRCh38.p7	2:151677716	ACGTCGAGACTGCCA[A/G]TAGGAATCCAGCCAA	4703
rs201154794	snp	A/G	1.65671e-05	0.00287807	missense, intron-variant	NEB	GRCh38.p7	2:151650815	GACAACACAAGTTTT[A/G]GGTCATCTTGCAGAC	4703
rs201161533	snp	A/T	0.00299547	0.0385845	intron-variant	NEB	GRCh38.p7	2:151538079	GGTTGCTAAAAAATA[A/T]ATGTATATGTATATG	4703
rs201167928	snp	C/T	0.00299544	0.0385843	missense	NEB	GRCh38.p7	2:151655855	GCTTGGCAAGCACCA[C/T]GTCCATGGAATCAGT	4703
rs201169452	snp	A/T	0.00091086	0.0213214	missense	NEB	GRCh38.p7	2:151672462	CTGTTTGTAGTTGAC[A/T]TTGGTAGCGACATCC	4703
rs201173663	snp	A/G	0.000216182	0.0103944	intron-variant	NEB	GRCh38.p7	2:151538255	CGTAGCTAGAAAGAG[A/G]AAAAACACATGAATT	4703
rs201176536	snp	C/T	0.000480596	0.0154941	intron-variant	NEB	GRCh38.p7	2:151547559	AAAAATACCCCAAAA[C/T]ATATGTATTAGAGAC	4703
rs201176993	snp	C/G/T	0.00117518	0.0242117	missense, intron-variant	NEB	GRCh38.p7	2:151633913	TCATCTTCAATGTTC[C/G/T]GGGCTCCAATATGGT	4703
rs201177994	in-del	-/A			intron-variant	NEB	GRCh38.p7	2:151538644	AAGTTCATTTGAGAG[-/A]AAAAAAAAAACCCAA	4703
rs201180226	snp	A/G	0.00245497	0.0349493	intron-variant	NEB	GRCh38.p7	2:151665554	TCTTTACAATGAGAA[A/G]AAAAATTTCATTTCA	4703
rs201189784	snp	C/T	0.000544361	0.0164889	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151512801	CCACAGAAGTGAAAT[C/T]GGCTTTCTCCATTTC	4703
rs201218741	in-del	-/A			intron-variant	NEB	GRCh38.p7	2:151632316	ACAAAAAAAAAAAAA[-/A]CTATTAGAATTAGCC	4703
rs201219620	snp	C/T	0.000145484	0.00852764	intron-variant	NEB	GRCh38.p7	2:151567133	TCAGAGTGTACCATG[C/T]GTTTCTAGATAATGA	4703
rs201221209	snp	A/C			missense, intron-variant	NEB	GRCh38.p7	2:151650743	GAGAACTTAGTTTTC[A/C]ACTTCTCAAAGTCCT	4703
rs201224940	snp	C/G/T	1.65773e-05	0.00287895	intron-variant	NEB	GRCh38.p7	2:151687549	TGCAAAGACATCACA[C/G/T]ATGCCAGATCCCACT	4703
rs201225181	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151579084	AGACTCCATCTCAAA[A/G]AAAAAAAAAAAAAAA	4703
rs201225445	snp	C/G	0.0382395	0.132881	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151600604	AGGGATGGAGATCTT[C/G]GCTTTGTGGTCGTTG	4703
rs201232044	snp	A/G			intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151499040	AAGCAGTATAAATGT[A/G]GATGCTTAGACACTG	4703
rs201235129	in-del	-/TTGA			intron-variant	NEB	GRCh38.p7	2:151574285	GGCATGTTCTTACTC[-/TTGA]GTAATTATATTAGCA	4703
rs201243201	snp	G/T	0.000399281	0.0141238	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151493815	TTCACTCTTTCCATC[G/T]CAGGAGTAAAGGGTG	4703
rs201250579	snp	C/T	0.00083022	0.0203573	intron-variant	NEB	GRCh38.p7	2:151618263	ATCTAACAGTGAGGA[C/T]TGAAGACTCACCTTA	4703
rs201272155	in-del	-/A			intron-variant	NEB	GRCh38.p7	2:151639466	CCACAAAAACTTTAT[-/A]AAAAAAAAAGAAAAG	4703
rs201272410	in-del	-/TATATATATATTTTTTTT			intron-variant	NEB	GRCh38.p7	2:151576507	ATATATATATATATA[-/TATATATATATTTTTTTT]TTTTTTTTTTTTTTT	4703
rs201286491	snp	C/T			synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151494176	CGAGCTAATGTTTTC[C/T]TGATTGCGTTTGACT	4703
rs201288341	snp	C/T	0.000215341	0.0103742	missense, intron-variant	NEB	GRCh38.p7	2:151629550	TCACATCACTGATAA[C/T]GTCCCTGGAGGCCTT	4703
rs201290038	in-del	-/T	0.04299	0.140167	intron-variant	NEB, RIF1	GRCh38.p7	2:151502763	AATAAAATTAAGGGA[-/T]TTTTTTTTTTTTGGC	4703
rs201291446	snp	C/T	0.000298855	0.0122204	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151493797	AAGTTTTCTTGATTG[C/T]GTTTCACTCTTTCCA	4703
rs201293220	in-del	-/AA	0.0221141	0.102801	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151498951	AGAAAAGGTTAGAAT[-/AA]AAGAAACGAGGATAA	4703
rs201297872	snp	A/G	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151607109	AAGTTTCTGCTAAAG[A/G]GTTGTGACATAGATA	4703
rs201305344	snp	C/T	4.52253e-05	0.00475506	intron-variant	NEB	GRCh38.p7	2:151723348	GTTCCCCTGACTCTG[C/T]ACACCTAAGTGGTGC	4703
rs201317374	in-del	-/A	0.0410537	0.137264	intron-variant	NEB	GRCh38.p7	2:151627419	ATGAGCAGAGAGAAG[-/A]AATGTCATCCCTTCT	4703
rs201337732	snp	C/T	0.000269924	0.0116142	missense	NEB	GRCh38.p7	2:151547684	GGATCTCAGGGGTAT[C/T]GGGAGTTGTATGGAT	4703
rs201345781	snp	C/T	1.65597e-05	0.00287743	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151627670	TCCCAGCATGTCCAC[C/T]GGGCTGCTGAACTTG	4703
rs201359707	in-del	-/TG			intron-variant	NEB	GRCh38.p7	2:151572946	AACATGGGAAAATTT[-/TG]CTTAACTTTTAAAAA	4703
rs201360854	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151659493	TTTTGTAGAGATGGG[G/T]TTTTGCCATGTTGCC	4703
rs201365253	in-del	-/CT	0.00914312	0.0669923	intron-variant	NEB	GRCh38.p7	2:151719172	CCTCTTGACTGTGAG[-/CT]CTCTGGGATGGCAAA	4703
rs201365821	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151580385	GTGGAAAAAAACAGT[A/G]TATTTCTAGCACACA	4703
rs201374063	snp	A/G	0.00299545	0.0385843	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151501443	ATCTCAGGAGTGACA[A/G]GTAGGGGAGTCCCCT	4703
rs201384911	snp	C/T	0.00299551	0.0385848	intron-variant	NEB	GRCh38.p7	2:151591296	ATTAAGTTAAACTCC[C/T]TCTATTTCTACTAGT	4703
rs201389582	snp	C/T	6.88931e-05	0.00586871	missense	NEB	GRCh38.p7	2:151666091	TAACCAGTACATACA[C/T]CACTCTGAATCTGCA	4703
rs201399589	snp	A/G	0.0039921	0.0444985	intron-variant	NEB	GRCh38.p7	2:151560945	CCCATTTATTCTCTT[A/G]CTGTCCCAGAAGGGG	4703
rs201400523	snp	C/T	0.00230715	0.0338859	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151526203	CAGCAGGATCTGAGG[C/T]GTGTCAGGTACGGCA	4703
rs201413627	snp	C/G/T	0.178465	0.239547	intron-variant	NEB	GRCh38.p7	2:151675771	CCTAGAGAGAAAGTA[C/G/T]TAGTTAGAATAAGTT	4703
rs201416585	in-del	-/A			intron-variant	NEB, RIF1	GRCh38.p7	2:151503618	CTTTTCCAAAATAGT[-/A]AAAATTTTTACTACT	4703
rs201416685	snp	A/G	4.96808e-05	0.00498377	missense, intron-variant	NEB	GRCh38.p7	2:151614454	GTCTTCCACTTCTCA[A/G]ACTCCTTCTTGTACT	4703
rs201419564	snp	A/G	0.000405721	0.0142371	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151502816	AGTTCTCTTGATTGC[A/G]TTTGACTCTCTCCAT	4703
rs201420007	snp	A/C/T	3.31225e-05	0.00406941	synonymous-codon	NEB	GRCh38.p7	2:151677643	AAATTTGAGGGTGTC[A/C/T]GGATGTTGCCTGTAC	4703
rs201423455	snp	A/G	0.00268078	0.036513	intron-variant	NEB	GRCh38.p7	2:151576398	GGTTTGTGTTTTGTT[A/G]TGTATGTGTGTGGTA	4703
rs201426239	snp	A/G	0.000563296	0.0167729	missense, intron-variant	NEB	GRCh38.p7	2:151618327	TGCTCCGGAGTGTCC[A/G]TTATACTGGTAAATT	4703
rs201429250	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151699818	TTTTGTAGGTTGCCT[C/G]TTCACTCTGATGGTA	4703
rs201433028	snp	C/T	0.000280204	0.0118331	missense	NEB	GRCh38.p7	2:151724286	TGGCGGTGTTCTTAA[C/T]GGCCTGGACAAGTTC	4703
rs201445278	snp	C/T			missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151493788	ACCGAGCTAAAGTTT[C/T]CTTGATTGCGTTTCA	4703
rs201456787	snp	G/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151495741	CACTTTCATTTTTAA[G/T]TAAGTAAATTGATAA	4703
rs201460418	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151558327	TCTGAAGGACCTCTT[C/T]AAGGAGAACTACAAA	4703
rs201462794	snp	A/G	0.000263314	0.0114712	missense	NEB	GRCh38.p7	2:151565105	GTATCTGGTGAAAAC[A/G]TATATTTGCCCTTTG	4703
rs201468807	snp	A/T	0.00299544	0.0385843	missense	NEB	GRCh38.p7	2:151682739	AGCCACAACCTTTCA[A/T]CCAGCTATTGTAGTC	4703
rs201473194	snp	A/G	0.000355393	0.0133255	missense	NEB	GRCh38.p7	2:151727692	TGTTTGAAACTTACT[A/G]GGCTAAAAAGATCCT	4703
rs201473873	snp	A/G	0.000350435	0.0132323	intron-variant	NEB	GRCh38.p7	2:151555054	TTTGATCTATAGAGA[A/G]TAAGTAGAAAGGAAG	4703
rs201482443	in-del	-/TGAG	0.00415014	0.0453635	intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151497067	CCAGAAAAACAACCA[-/TGAG]TGAGTAACATTTCAT	4703
rs201482825	snp	A/C/T	4.4506e-05	0.00471714	intron-variant	NEB, RIF1	GRCh38.p7	2:151516432	TGTGATGGATCATTG[A/C/T]TGTGTGGTGTGGTTT	4703
rs201483656	snp	A/C/G/T	0.000132701	0.00814475	missense, intron-variant	NEB	GRCh38.p7	2:151612236	CAATTTCCGGAGTGT[A/C/G/T]GGTAATGCATGTGAA	4703
rs201498216	snp	C/T	0.00299544	0.0385843	missense	NEB	GRCh38.p7	2:151688341	ATAAACTGTGGAGCA[C/T]CTGCTGGTATATGGC	4703
rs201515651	snp	A/G	0.00016578	0.00910288	synonymous-codon	NEB	GRCh38.p7	2:151553455	AGGAGTGTCCCAGAC[A/G]TAGCAACCAATGCCT	4703
rs201529683	snp	A/G	0.000192734	0.00981478	missense	NEB	GRCh38.p7	2:151563914	TTGGTGCCCTCCCAC[A/G]CCCCTTTATACAGTA	4703
rs201536366	snp	A/G	1.72412e-05	0.00293604	intron-variant	NEB, RIF1	GRCh38.p7	2:151529335	GGAGGAAACACAGTG[A/G]CAAGATTAATTTTTT	4703
rs201539560	snp	C/T			synonymous-codon	NEB	GRCh38.p7	2:151663740	ATATCCCTTCTTGTA[C/T]TCCCGGTCTGACTGC	4703
rs201539722	snp	G/T	7.26599e-05	0.00602699	missense	NEB	GRCh38.p7	2:151545932	CTTTTCTGTATTCTG[G/T]AGTGTCAAGCACCAC	4703
rs201541240	snp	A/C/T	0.000182204	0.00954309	missense	NEB	GRCh38.p7	2:151677623	GGGGAGTCCACAATG[A/C/T]TGGTAAATTTGAGGG	4703
rs201545521	snp	A/G	0.000877374	0.0209265	missense	NEB	GRCh38.p7	2:151671066	GCCAACACCATGCCC[A/G]TGGAATCAGGCACAC	4703
rs201548700	snp	C/T	0.000232311	0.010775	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151525248	GATTTTCCTTTCTCC[C/T]TGACAAACTTCTTTT	4703
rs201553266	snp	C/T	3.38341e-05	0.00411289	synonymous-codon	NEB	GRCh38.p7	2:151551738	GTTCTCACTGCTCAC[C/T]GAACTCTGGAGCTTG	4703
rs201566336	snp	A/G	0.000257782	0.0113501	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151494170	CAATACCGAGCTAAT[A/G]TTTTCTTGATTGCGT	4703
rs201575525	in-del	-/C			intron-variant	NEB	GRCh38.p7	2:151556778	GAGACTTTAACACCT[-/C]CCTGTCGACACTAGA	4703
rs201575629	snp	C/T	0.496999	0.0386216	intron-variant	NEB	GRCh38.p7	2:151702171	TTCCATGTAGTTGAG[C/T]GGTTTTGAGTGAGAT	4703
rs201577560	in-del	-/A	0.0158469	0.0875917	intron-variant	NEB	GRCh38.p7	2:151658591	ACTATGATTAGGATG[-/A]AAAAAGGAAATGAAA	4703
rs201579869	snp	A/G	0.00685063	0.0581239	intron-variant	NEB	GRCh38.p7	2:151535669	TGAATAGGCTTAATT[A/G]GAGCAGTTTATTCAT	4703
rs201585290	snp	C/T	0.000151469	0.00870125	intron-variant	NEB	GRCh38.p7	2:151642914	TAGGCCAGTAATAAA[C/T]AGACACATGCAGACA	4703
rs201588466	snp	G/T	7.05542e-05	0.00593903	intron-variant	NEB	GRCh38.p7	2:151707020	AGTGAAATAAAATGA[G/T]AAAGTAACTCTATGG	4703
rs201596787	snp	A/G	0.000198771	0.00996724	missense, intron-variant	NEB	GRCh38.p7	2:151627091	TGTCCGGAGGCTGGC[A/G]GTAGATGTTATCACT	4703
rs201609120	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151700070	GGGATCCAGTTTCAG[A/C]TTTCTACATATGGCT	4703
rs201614105	snp	A/G	6.63812e-05	0.00576075	missense, intron-variant	NEB	GRCh38.p7	2:151618426	ACTTCCAAGGAATCA[A/G]TCGGAACCCAGCCAA	4703
rs201622661	snp	A/G	6.62745e-05	0.00575612	synonymous-codon	NEB	GRCh38.p7	2:151562167	GGGTGTATCCCAAAC[A/G]TAGCAACCAATGCCT	4703
rs201623736	snp	A/C			intron-variant	NEB, RIF1	GRCh38.p7	2:151532757	TTAACTTTTTTTTTT[A/C]GGTCTGGGAAAAATG	4703
rs201624046	snp	A/T	1.66103e-05	0.00288182	missense	NEB	GRCh38.p7	2:151697599	TTGGGGGTCTCGCAG[A/T]AATTTATGCTCTTTG	4703
rs201625994	snp	C/T			missense, intron-variant	NEB	GRCh38.p7	2:151646212	TGAGTCTTGTCTTTG[C/T]CCCAAGCTTCTCTAT	4703
rs201634621	snp	A/G	3.31516e-05	0.0040712	intron-variant	NEB, RIF1	GRCh38.p7	2:151531906	TTTGATCTAAATTGT[A/G]GAAGAGAAGAAAGAG	4703
rs201636991	snp	A/C/T	2.70077e-05	0.00367466	stop-gained, missense	NEB	GRCh38.p7	2:151664588	CTTCTTTTCCTCTTC[A/C/T]CAGCCAGCTTTGTAC	4703
rs201646087	snp	A/C/T	0.000127596	0.00798648	intron-variant	NEB	GRCh38.p7	2:151682633	CAACACAGTCACCAC[A/C/T]CTCCCTCTGACACAC	4703
rs201650096	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151512289	TCCACCCACCTCGGC[C/T]TCCCAAAGTGCTGGG	4703
rs201683981	in-del	-/A	0.000281942	0.0118698	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151498379	GAAAGCATCCAGAAC[-/A]AAAAAAGCAATCAAT	4703
rs201684605	snp	C/T	0.00140119	0.0264316	intron-variant	NEB	GRCh38.p7	2:151546338	CATTGTGATGATGTG[C/T]ACTCACCCAGAGCTT	4703
rs201688876	snp	C/T	0.000867853	0.0208128	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151519013	ATTCATGATCAGAGA[C/T]TCCTTCATGTCAGTC	4703
rs201690442	snp	A/G	6.53381e-05	0.00571531	intron-variant	NEB	GRCh38.p7	2:151565839	AGAGCAGGAAGAGAG[A/G]TATAATGGAGGAATA	4703
rs201690610	snp	C/T	6.63075e-05	0.00575755	missense, intron-variant	NEB	GRCh38.p7	2:151650325	CTGCCTCTAAAGAAC[C/T]CAAGGGACTCCATCC	4703
rs201695184	snp	A/G			missense, intron-variant	NEB	GRCh38.p7	2:151650731	TCCACTGGGCTGGAG[A/G]ACTTAGTTTTCCACT	4703
rs201698008	snp	A/C	0.000794886	0.0199201	synonymous-codon	NEB	GRCh38.p7	2:151687452	TGTCTTCAAGGAGTG[A/C]AGCATCTTTGGATCG	4703
rs201707021	snp	C/T	0.000711926	0.0188535	missense, intron-variant	NEB	GRCh38.p7	2:151640027	ACACCCAGCCAATGC[C/T]TCTCATCCACTGGAG	4703
rs201707392	snp	C/T	0.000309621	0.0124384	intron-variant	NEB, RIF1	GRCh38.p7	2:151519100	GAAGAAAGGAAATCA[C/T]GTAAATAGGAAATGG	4703
rs201714437	snp	C/T	0.000563063	0.0167695	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151485875	ATGGCATCTCCATCC[C/T]TGAAGGACACCTCAT	4703
rs201719702	snp	C/T			stop-gained, intron-variant	NEB	GRCh38.p7	2:151612363	TCCTATGCCTCTCAG[C/T]CACTCAAGATCAGAT	4703
rs201731351	snp	A/C/T	8.33807e-05	0.00645637	missense	NEB	GRCh38.p7	2:151553878	CATTGACTTGCAAGT[A/C/T]GGGGTGGCAAATCCA	4703
rs201732607	snp	C/T	0.00157279	0.0279986	missense, intron-variant	NEB	GRCh38.p7	2:151591389	TGGCATGCTGGATCC[C/T]AATGGCATCTGCTCG	4703
rs201732664	snp	A/G	1.65644e-05	0.00287783	intron-variant	NEB, RIF1	GRCh38.p7	2:151526073	TTGTACTTGTTCTGG[A/G]GGAATCCATAGAGAG	4703
rs201734774	snp	A/T	0.000303767	0.0123204	missense	NEB	GRCh38.p7	2:151570579	CCCGCCTTCATTTCA[A/T]CCCAGCCCTCACGGT	4703
rs201735545	snp	A/G	4.98799e-05	0.00499374	synonymous-codon	NEB	GRCh38.p7	2:151727733	ACTGTGTGCAATGTA[A/G]GGGGTCATGAACTTT	4703
rs201738560	snp	C/T	1.71587e-05	0.002929	missense	NEB	GRCh38.p7	2:151655319	AAAATATCTGGTGTA[C/T]CAGGCATCACATGAA	4703
rs201741126	in-del	-/ATATATATA			intron-variant	NEB	GRCh38.p7	2:151576508	TATATATATATATAT[-/ATATATATA]TTTTTTTTTTTTTTT	4703
rs201746137	snp	C/T	0.000745163	0.019288	missense, intron-variant	NEB	GRCh38.p7	2:151643271	AAAATCTGGGTGGCT[C/T]GTTTATTTTTCTCAT	4703
rs201747395	snp	C/T	0.000267971	0.0115721	missense, intron-variant	NEB	GRCh38.p7	2:151642591	CACTTGCAATATCTC[C/T]GGAGGCCTTGGCTGC	4703
rs201751179	snp	G/T	0.0039921	0.0444985	intron-variant	NEB	GRCh38.p7	2:151551731	CTCTCAAGTTCTCAC[G/T]GCTCACCGAACTCTG	4703
rs201758329	snp	A/G	0.000106707	0.00730355	missense	NEB	GRCh38.p7	2:151656167	CATCACTCTGTATGC[A/G]ATTCATATTCCTGGT	4703
rs201761956	snp	C/T	0.0039921	0.0444985	missense	NEB	GRCh38.p7	2:151663840	CCTTTGGCTTGTTCA[C/T]AGGCTTTCTTGTATT	4703
rs201767726	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151581966	AATGAGTCAGAAATA[C/T]GGTAGTAAAATTATT	4703
rs201767727	snp	A/G	0.00349604	0.0416629	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151512812	AAATTGGCTTTCTCC[A/G]TTTCTGCTGATTGCT	4703
rs201774719	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151559102	TTTACAAGAAAAAAA[A/C]AAACAACCCCATCAA	4703
rs201780892	in-del	-/G	0.0228947	0.104514	intron-variant	NEB, RIF1	GRCh38.p7	2:151531648	GGGGAGGAGAATCCT[-/G]TGCATAACAGGACAT	4703
rs201792803	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151594747	TAACATATATTCCAG[A/T]TGGGGAAAACAAGGC	4703
rs201795802	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151635575	TATGGGCGTGGTGGT[G/T]AGTGCCTGTAATCCC	4703
rs201797283	snp	A/T	6.34256e-05	0.00563106	intron-variant	NEB	GRCh38.p7	2:151694643	TTCTGGACAAAAAAA[A/T]TCAGCAAAGGAATTG	4703
rs201804220	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151577837	CCCACCTCAGCCTCC[C/G]CAAAGTGCTGAGATT	4703
rs201825451	snp	A/G	0.00276309	0.0370663	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151492120	AGTCTCCTGATCTTG[A/G]TCATTCCGTTTTTGT	4703
rs201836097	in-del	-/AACTT			intron-variant	NEB, RIF1	GRCh38.p7	2:151486595	CCAAAAAGTGGAAAC[-/AACTT]AAATGCCCACCAACT	4703
rs201847731	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151601111	CTTTTCTTTTCTTTT[C/T]TTTTTTTTTTTTTTG	4703
rs201869942	snp	C/T	1.66123e-05	0.00288199	intron-variant	NEB	GRCh38.p7	2:151692235	GAAAGCCCTCCTACC[C/T]GAAAGGTAACCGTGG	4703
rs201874451	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151546897	GTTTACTTGCACCCA[A/C]ATAAGTCATGTTTTT	4703
rs201877927	in-del	-/T	0.0252325	0.109451	intron-variant	NEB	GRCh38.p7	2:151698217	AATTTTTTTTCTTTC[-/T]TTTTTTTGTAACAGC	4703
rs201885553	in-del	-/T	0.0341408	0.126114	intron-variant	NEB	GRCh38.p7	2:151682994	ATCCTTATTTCCAAC[-/T]TAATGGAAGTCTGTG	4703
rs201886728	snp	C/T	0.000789066	0.0198472	missense	NEB	GRCh38.p7	2:151562640	CCTGGGCGTTTCGGA[C/T]GCGTATAACATTGGG	4703
rs201895549	snp	G/T	0.00299545	0.0385843	missense	NEB	GRCh38.p7	2:151567173	AATCACTTACATCAC[G/T]CTGTAGGTCATAGGC	4703
rs201896003	snp	A/C/T	6.62662e-05	0.00575581	synonymous-codon	NEB	GRCh38.p7	2:151679766	AGCTCTGATGGGAAT[A/C/T]GCATCAGTTCTCAGG	4703
rs201897684	snp	C/T	6.11378e-05	0.00552858	intron-variant	NEB, RIF1	GRCh38.p7	2:151527439	ATTGTATTTCTCAGG[C/T]GCAGTATGCAGTTAC	4703
rs201903214	snp	G/T	0.0039921	0.0444985	missense	NEB	GRCh38.p7	2:151662151	TCGTTCATAATTTTT[G/T]CATTATTCTGGGCCA	4703
rs201923569	snp	A/C			intron-variant	NEB, RIF1	GRCh38.p7	2:151495462	GATGCGTGCTAATGT[A/C]TTAGAAGCACTGTAC	4703
rs201934608	snp	A/C	0.0029954	0.038584	intron-variant	NEB, RIF1	GRCh38.p7	2:151490093	CTGAAAAAAAGGGGG[A/C]AAATTCTTTATAAGA	4703
rs201940342	snp	C/T	0.000166066	0.00911073	missense	NEB	GRCh38.p7	2:151663688	CCACCACACTGAGCA[C/T]GTCCACCGGGGTGTG	4703
rs201940775	snp	A/C			intron-variant	NEB, RIF1	GRCh38.p7	2:151502400	CATAAAAAAAAAAAA[A/C]CTTAAAAGCTGCAAA	4703
rs201941010	snp	C/T	0.00299544	0.0385843	NEB	2	allele_origin=T(somatic)/C(germline)	2:151724910	TATCCTTTGCTTTTT[C/T]ATCTACGTGACATAT	4703
rs201949169	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151576051	AATAAAATTTTTGTT[A/T]TTAATAAAGTTTTTA	4703
rs201961566	snp	C/T	5.30743e-05	0.00515115	intron-variant	NEB, RIF1	GRCh38.p7	2:151527040	GTGATAGAAGAAAGG[C/T]AGAAGAAAAGGGAAG	4703
rs201962649	snp	C/T	0.000530381	0.016276	missense	NEB	GRCh38.p7	2:151569293	ATGTCCGCGGCATGT[C/T]TGGCATGATTGACGG	4703
rs201964096	in-del	-/CTACGTAGGGT	0.00874735	0.0655527	intron-variant	NEB	GRCh38.p7	2:151563491	AATCTCAGGAAGGAC[-/CTACGTAGGGT]CCTACGCTACTCCAT	4703
rs201964719	snp	C/T	1.66015e-05	0.00288105	missense	NEB	GRCh38.p7	2:151655998	AGCCCTTTGTACCAT[C/T]CATTGTAATCTTGCT	4703
rs201964885	snp	C/T	1.66674e-05	0.00288676	intron-variant	NEB	GRCh38.p7	2:151538091	ATATATGTATATGTA[C/T]ATGGTGAGTTGTAGA	4703
rs201965465	snp	C/T	1.65625e-05	0.00287766	missense, intron-variant	NEB	GRCh38.p7	2:151627782	TCATCTTCAATGTTC[C/T]GGGCTCCAATGTGGT	4703
rs201968290	snp	C/G	1.92643e-05	0.00310351	missense	NEB	GRCh38.p7	2:151664837	AATGGTGGTCTTGTC[C/G]TTGTTCCATTTTTCA	4703
rs201968673	snp	C/T	8.54032e-05	0.00653409	synonymous-codon	NEB	GRCh38.p7	2:151665528	ATTGGTGAAGTCAGA[C/T]TTGTACAGATTCTTT	4703
rs201971223	snp	G/T	0.00142162	0.0266231	missense	NEB	GRCh38.p7	2:151565051	GAACTTACAGTACTG[G/T]AGAGTTTTCCCATGT	4703
rs201976154	snp	C/T	0.000417554	0.0144431	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151519018	TGATCAGAGACTCCT[C/T]CATGTCAGTCACGGG	4703
rs201979610	snp	C/G	0.00380415	0.0434466	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151529260	TGATATGAACAGCAT[C/G]TGGCTCAATGGTGCA	4703
rs201983142	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151631112	AACATCTTCTGGCAT[C/T]TTGGAGAAGCTTAAG	4703
rs201984572	snp	C/T	6.62449e-05	0.00575483	missense	NEB	GRCh38.p7	2:151672565	TTCTTCTTGTATTCA[C/T]GATCAGACTGCAGCT	4703
rs201998031	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151608240	ATATGAGGTCAACAA[A/G]TATTTGTGTTCCTGA	4703
rs202003762	in-del	-/AG	0.0166325	0.0896639	intron-variant	NEB, RIF1	GRCh38.p7	2:151501831	TAGGGAACCAAAGAA[-/AG]AGGAGAGAGAGAGAC	4703
rs202009284	snp	A/G	0.0029954	0.038584	missense	NEB	GRCh38.p7	2:151575759	TCTGGCATTATGTGT[A/G]TTGAAGTTTTATCCT	4703
rs202017360	snp	C/T	0.00884677	0.0659175	missense, intron-variant	NEB	GRCh38.p7	2:151603751	TACCCTTCAGCCATT[C/T]CAGGTCTGACTTGTA	4703
rs202024824	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151546788	GGTCTCGAACTCCTG[A/T]CCTCAGGTGATCTGC	4703
rs202026890	snp	C/T	0.00012256	0.0078272	missense	NEB	GRCh38.p7	2:151684974	TCTTTTCGATATTCG[C/T]GCTGTGAATAGGAAA	4703
rs202034435	snp	C/T	5.84915e-05	0.00540762	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151514849	GTTGCATATTTGACA[C/T]GTAACAAAGCTGGCG	4703
rs202035863	snp	C/T	0.0129625	0.0794557	missense	NEB	GRCh38.p7	2:151710498	GGTGTCTCACTCCAT[C/T]TGCCTTTGATTTTAT	4703
rs202042541	snp	A/G	0.000399281	0.0141238	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151512767	ACTTGTTGGGCATGA[A/G]TGATCTCTGGAGTAT	4703
rs202044707	snp	A/G	9.93674e-05	0.00704796	missense, intron-variant	NEB	GRCh38.p7	2:151643239	GATCTGGGTGCTGAC[A/G]GTAAACATGGTCACT	4703
rs202048855	snp	C/G/T	0.0001456	0.00853129	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151494161	TTCTCAAGACAATAC[C/G/T]GAGCTAATGTTTTCT	4703
rs202050860	snp	A/G	0.000513343	0.0160127	NEB, RIF1	2	allele_origin=G(germline)/A(germline)	2:151524358	TTTCTATGTCTGGGC[A/G]ACCGAGCATGCTTAA	4703
rs202065132	snp	A/G			intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151499038	CAAAGCAGTATAAAT[A/G]TGGATGCTTAGACAC	4703
rs202068501	in-del	-/CAAA			intron-variant	NEB, RIF1	GRCh38.p7	2:151510431	CATTCATTTAGTACT[-/CAAA]CAGTTGTTAGTGAGA	4703
rs202072006	in-del	-/AAC	0.424037	0.179474	intron-variant	NEB	GRCh38.p7	2:151559104	TACAAGAAAAAAACA[-/AAC]AACCCCATCAAAAAG	4703
rs202073021	snp	G/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151495444	AACCCTGCACGTTAT[G/T]CTGATGCGTGCTAAT	4703
rs202074655	in-del	-/AAC	0.021333	0.101051	intron-variant	NEB	GRCh38.p7	2:151688727	GCACAGTAAGAGATT[-/AAC]AACAATAACTAATAA	4703
rs202082785	snp	A/G	6.65059e-05	0.00576616	intron-variant	NEB	GRCh38.p7	2:151618245	TCTGTGGTAACTTTC[A/G]GTATCTAACAGTGAG	4703
rs202085388	in-del	-/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151529534	TTTTTTTTTTTTTTT[-/T]AACAGATTCTCTCTC	4703
rs202085426	in-del	-/A	0.0329836	0.124112	intron-variant	NEB	GRCh38.p7	2:151725634	CTCACCCCATTTGAT[-/A]AAAAAAAAATCCTTC	4703
rs202111641	snp	C/T	5.11496e-05	0.00505689	missense	NEB	GRCh38.p7	2:151570308	TGTCAGCTATGAGGG[C/T]CCAGCGGATCTTGTT	4703
rs202113159	snp	A/C	0.00028614	0.0119578	missense	NEB	GRCh38.p7	2:151665346	ACCTTGTCCATGTTC[A/C]GTTTGTTACTCTTGT	4703
rs202118466	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151605505	AGAAGATAACAACAA[A/G]AGTTCTGTGGACAAG	4703
rs202124287	snp	C/T	0.00120824	0.0245491	missense	NEB	GRCh38.p7	2:151677702	TTTTAACTTTTTCGA[C/T]GTCGAGACTGCCAAT	4703
rs202133044	snp	C/T	0.00015614	0.00883435	intron-variant	NEB	GRCh38.p7	2:151565024	GAAATTGAGTGGTTA[C/T]TACATAAAAGAGAAC	4703
rs202137113	snp	A/G	0.000480571	0.0154937	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151502794	CCCCTAAGAAATACC[A/G]AGCTAAAGTTCTCTT	4703
rs202137722	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151704655	CCCTTTCTTTGAGTC[A/G]GAAAGGTAACTCTCT	4703
rs202139330	snp	G/T	0.00115961	0.0240512	missense	NEB	GRCh38.p7	2:151548367	CATCTTTGGGGCCAA[G/T]TGTATACCCATATGC	4703
rs202142644	snp	A/G	6.63416e-05	0.00575903	synonymous-codon	NEB	GRCh38.p7	2:151576346	CTCCAAGTCAGCCTT[A/G]TAGAGGGCCTGAAAA	4703
rs202144520	snp	C/G/T	1.65608e-05	0.00287752	synonymous-codon, missense	NEB	GRCh38.p7	2:151672552	GGTGTTCTCATAGTT[C/G/T]TTCTTGTATTCACGA	4703
rs202145313	snp	C/G	0.000250244	0.011183	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151492258	GCAACCCTTGTGTTT[C/G]TCAAAGTCTTCATGA	4703
rs202148108	snp	A/G	0.000149225	0.00863657	intron-variant	NEB	GRCh38.p7	2:151575815	CTGTGGAAAGAAACA[A/G]AAATAATAAAATTAC	4703
rs202149495	snp	C/T			missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151493786	ATACCGAGCTAAAGT[C/T]TTCTTGATTGCGTTT	4703
rs202159633	snp	C/T	1.65853e-05	0.00287964	synonymous-codon	NEB	GRCh38.p7	2:151710467	ATTCATTCTGGCATT[C/T]GCAACTTCAAAGCAA	4703
rs202172327	snp	C/T	1.6582e-05	0.00287936	synonymous-codon, intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151534269	TCTAGGCTCATCGAC[C/T]ACCAGGTGGTATTTA	4703
rs202191938	snp	A/G	0.000281562	0.0118618	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151506167	CACTGTGTCTTTACC[A/G]AGCTAATGTGGTCCT	4703
rs202207189	snp	C/T	1.65787e-05	0.00287907	missense	NEB	GRCh38.p7	2:151674568	ATTAAGTCATACCAA[C/T]CCCGTTTATAACAGA	4703
rs202209668	snp	A/G	0.00069972	0.0186915	missense	NEB	GRCh38.p7	2:151541475	TTCTGCCCTCGCTTG[A/G]CTCTTAAAAGATCAG	4703
rs202211102	snp	A/G	0.000248416	0.0111421	missense	NEB	GRCh38.p7	2:151563653	GAACCACACCAGGGA[A/G]TTCACCGATCACTTT	4703
rs202232547	snp	A/T	0.000350933	0.0132417	intron-variant	NEB, RIF1	GRCh38.p7	2:151529174	ACAGAAGCTGGTAAA[A/T]CCCCCACCATGCTTG	4703
rs202233025	snp	A/C	1.65745e-05	0.00287871	missense, intron-variant	NEB	GRCh38.p7	2:151650295	TGATGATTTCCGAAG[A/C]CCGCTTGTTCTTTTC	4703
rs202234374	snp	A/G/T	0.000995181	0.0222848	missense	NEB	GRCh38.p7	2:151663615	GGAAGCATGTTGTAG[A/G/T]TATGGATCACGTTCC	4703
rs202245789	snp	C/T	0.00299545	0.0385843	missense, intron-variant	NEB	GRCh38.p7	2:151646186	CAGGTGTATCAGGCA[C/T]GATGTGGATCTGAGT	4703
rs207462557	snp	C/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151524646	AAAATGTTTACTCAA[C/G]AGAGAGGCTTTTTTT	4703
rs267598917	snp	C/T			synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151492153	CATTTCTACCACTTT[C/T]CTCTGAATACCTCGG	4703
rs267598918	snp	C/T			synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151526236	GCAGGTTCCTCTTTC[C/T]TTGACATGTTTCTCT	4703
rs267598919	snp	A/G			synonymous-codon	NEB	GRCh38.p7	2:151562152	GGCATGGAGGATTTG[A/G]GGTGTATCCCAAACG	4703
rs267598920	snp	A/G			missense	NEB	GRCh38.p7	2:151562153	GCATGGAGGATTTGG[A/G]GTGTATCCCAAACGT	4703
rs267598921	snp	C/T			missense	NEB	GRCh38.p7	2:151562160	GGATTTGGGGTGTAT[C/T]CCAAACGTAGCAACC	4703
rs267598922	snp	G/T			missense, intron-variant	NEB	GRCh38.p7	2:151616076	AGTCATAGCCTTCCT[G/T]CTTGGACTCTTCCAA	4703
rs267598923	snp	C/T	1.66153e-05	0.00288225	NEB	2	allele_origin=T(somatic)/C(germline)	2:151656012	TTCATTGTAATCTTG[C/T]TTATATTCATTCTAT	4703
rs267598924	snp	A/G			missense	NEB	GRCh38.p7	2:151671178	CCAGGGAACCAATAG[A/G]GATCCATCCGATGCC	4703
rs267598925	snp	A/G			missense	NEB	GRCh38.p7	2:151696653	TCACTCAGTTGTTTG[A/G]AATTGACTTGGGCTT	4703
rs267598926	snp	C/T	9.97888e-05	0.00706289	NEB	2	allele_origin=T(somatic)/C(germline)	2:151717466	CTATATCTGGAGGAT[C/T]AGCCAGAGGCGTGAA	4703
rs367564407	snp	G/T	1.6563e-05	0.00287771	missense	NEB	GRCh38.p7	2:151694351	TTGGCCACCTTCAAG[G/T]AGTGCAGCATCTTGG	4703
rs367581295	snp	C/T	3.38524e-05	0.00411401	synonymous-codon	NEB	GRCh38.p7	2:151724866	CCTTACCTTACTGAC[C/T]TGCTGCGACACTTTC	4703
rs367585270	snp	A/T	6.6807e-05	0.00577919	intron-variant	NEB	GRCh38.p7	2:151687387	ACAGGGAGTCCATCT[A/T]GAAAACAAGACAGAT	4703
rs367587065	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151486197	AGGCAAAGGATATGA[A/G]TAGACATTTCTCCAA	4703
rs367588674	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151655475	ATGCACTCAATTTGA[C/T]GTAGTAAGTAATAAC	4703
rs367588710	snp	A/G	1.92158e-05	0.0030996	intron-variant	NEB	GRCh38.p7	2:151667762	TCTTGAACTCCTGAA[A/G]TCTTTTAGATAGAAA	4703
rs367591953	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151635303	AACATAAGATTCCAA[C/T]ATAAAGGACAGCAAG	4703
rs367593747	snp	A/T	1.65938e-05	0.00288039	missense	NEB	GRCh38.p7	2:151697552	TGCTTACATCACTAC[A/T]GAAGTTCTGCAGAAC	4703
rs367594330	snp	G/T	3.31719e-05	0.00407245	missense	NEB	GRCh38.p7	2:151672640	CTTCTGAAACCCACA[G/T]GCTTTCCCTTTGACT	4703
rs367599472	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151613639	AGATCTCATGTTGAA[C/T]TGTAATCCTCAATGT	4703
rs367607601	snp	G/T	1.65968e-05	0.00288065	synonymous-codon	NEB	GRCh38.p7	2:151663647	GTAGTTGGCATTGGT[G/T]GCCACTTCCTGAGAC	4703
rs367610538	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151622386	ATTTAAAAAATGAAA[C/T]CTTTATATTATCACA	4703
rs367610955	snp	C/T	0.000165986	0.00910855	intron-variant	NEB, RIF1	GRCh38.p7	2:151492325	AATATGATGGTGTGA[C/T]TATATCCCTTTTTAC	4703
rs367619283	snp	C/T	8.3002e-05	0.00644159	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151639923	AGTCACACTGGTAAA[C/T]TTGAATCTGTCTGGA	4703
rs367621870	in-del	-/GTGG			intron-variant	NEB	GRCh38.p7	2:151638837	TGTGTGTGTGTGTGT[-/GTGG]GTTACCTGGTAGTAC	4703
rs367626762	snp	A/G	0.000473649	0.0153818	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151527524	GCCTGGAGGAAGTCC[A/G]GTCGGTCAGGAGTCC	4703
rs367627899	snp	C/T	0.000119263	0.00772122	missense, intron-variant	NEB	GRCh38.p7	2:151625637	GCTTCTGTGTATAAG[C/T]GCTGTGAAGGATAAA	4703
rs367630355	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151669210	GAGACTCCTTTAAAA[C/T]GGAAGGCTATCATTT	4703
rs367633538	snp	C/G	1.65916e-05	0.00288019	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151503382	ATTGCGTTTGACTCT[C/G]TCAATCTCTGGAGTC	4703
rs367638234	snp	C/G/T	6.80138e-05	0.0058312	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151609860	AATGTCGTTTTGATC[C/G/T]GGCATGCATGTCCAT	4703
rs367642307	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151638477	GCTCTCCATCTCTGG[A/G]GGTTGGCACAGATTT	4703
rs367643586	in-del	-/T	0.32885	0.23724	intron-variant	NEB	GRCh38.p7	2:151579186	ACAATGAAAACTTTC[-/T]GAAGAAACCTGGCTG	4703
rs367646560	snp	A/G/T	3.32703e-05	0.00407851	missense, synonymous-codon	NEB	GRCh38.p7	2:151553882	GACTTGCAAGTCGGG[A/G/T]TGGCAAATCCATTCG	4703
rs367648012	snp	A/C	2.52931e-05	0.00355611	intron-variant	NEB	GRCh38.p7	2:151565654	ACCACCACAGGTTAT[A/C]TACCCCAACATGGCA	4703
rs367652956	in-del	-/A	0.00795532	0.062565	intron-variant	NEB	GRCh38.p7	2:151538718	AAGGGAAAAAGGTTT[-/A]AGCTTCTAACTCCTA	4703
rs367668195	snp	C/T	3.32e-05	0.00407417	missense	NEB	GRCh38.p7	2:151541503	CAGGAGTATCAGGAA[C/T]TGAAGTAAAGATTGA	4703
rs367679749	snp	C/G	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151652770	TTATAGTTCATTTGA[C/G]AGTAAGATTTCAAAA	4703
rs367680989	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151654519	GCAATAAATGATGAA[A/G]TGCCTTTTATAAATT	4703
rs367690280	snp	C/T	0.00318978	0.0398085	intron-variant	NEB	GRCh38.p7	2:151548524	AAAAATTGCTCTTTT[C/T]AAGGATTAAGTATGT	4703
rs367733212	snp	G/T	3.31356e-05	0.00407022	missense, intron-variant	NEB	GRCh38.p7	2:151619572	GTCTGACACTTCTTG[G/T]CCAAAACGATACCAA	4703
rs367739638	snp	A/G/T	0.000182149	0.00954167	missense, synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151633723	CAGGCATGTCCACTC[A/G/T]TGCAGGTAGTTCTTA	4703
rs367755249	snp	A/G	5.32354e-05	0.00515896	intron-variant	NEB	GRCh38.p7	2:151610886	AGGGCAGGGCGGCAT[A/G]GGGCATGGGGAGAGG	4703
rs367755687	snp	A/G	0.000106532	0.00729759	intron-variant	NEB	GRCh38.p7	2:151568197	AAAGACAGAGCCACC[A/G]TAAAGGGTTAAAATG	4703
rs367773430	snp	C/T	4.34169e-05	0.00465903	missense	NEB	GRCh38.p7	2:151547431	ACGAGATGCTTACAT[C/T]ACTGGTGATGTCTCC	4703
rs367794943	in-del	-/CTCC	0.00478085	0.0486577	downstream-variant-500B, intron-variant	NEB, RIF1	GRCh38.p7	2:151485057	TTATGGTTGCTTCTT[-/CTCC]CTTTGCCTTTGCCAC	4703
rs367851383	snp	A/C	2.01217e-05	0.00317182	missense	NEB	GRCh38.p7	2:151560671	TAGCTGGTGGCTTTC[A/C]CTCTATCCCAGGCCT	4703
rs367853125	snp	A/T	2.76354e-05	0.00371711	synonymous-codon	NEB	GRCh38.p7	2:151547474	ATGGATCACTTGGGG[A/T]GTGTATGGCAGAGAG	4703
rs367881797	snp	C/T	0.119018	0.212941	intron-variant	NEB	GRCh38.p7	2:151581472	AAAGCAAATGATGTG[C/T]GCTGTCTTACATTGC	4703
rs367894816	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151668737	GACTAGGCACTCTTG[G/T]GTTTTCCAATCTTGT	4703
rs367906477	in-del	-/G			intron-variant	NEB	GRCh38.p7	2:151621694	ACAAATGTTCCATGG[-/G]AAGTGTCATTTGAGA	4703
rs367914393	snp	A/G	0.0023933	0.0345097	intron-variant	NEB, RIF1	GRCh38.p7	2:151529664	GCCTCCTGAGTACCT[A/G]GGACCACAGGCATGC	4703
rs367921141	snp	A/G			missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151505497	CTAATGTGCTTCTGC[A/G]TCTCCTTCACACGTT	4703
rs367923089	snp	A/C/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151540262	TAGAACTATGGATAT[A/C/G]GCTGAAATATGTTAT	4703
rs367960359	in-del	-/TCTTAAGCCAT			intron-variant	NEB	GRCh38.p7	2:151555570	GGGATAACAATTAGT[-/TCTTAAGCCAT]GTTGCCCGTTAATTA	4703
rs367988005	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151701465	CTCCTTGTACCTCTG[A/G]TAGAATTCGGCTGTG	4703
rs367997645	snp	C/T	0.000133023	0.00815437	synonymous-codon	NEB	GRCh38.p7	2:151692306	TTGATATTTTGGGGT[C/T]TCACAGTAATTCATA	4703
rs368021241	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151495924	TATTTAAGAAAGAGC[C/T]GCATTGGACCTACTC	4703
rs368025512	snp	C/T	1.75059e-05	0.00295849	intron-variant	NEB	GRCh38.p7	2:151672722	AGTCCTAGGCATTGA[C/T]AGCATTAGCGCTGCA	4703
rs368049677	in-del	G/TTATCCC			intron-variant	NEB	GRCh38.p7	2:151675771	CCTAGAGAGAAAGTA[G/TTATCCC]TAGTTAGAATAAGTT	4703
rs368073327	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151524887	TGGCCAGGCTGGTCT[C/T]GAACTCCTGACCTCG	4703
rs368074416	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151611413	TCCTATTGCTGTTAT[C/T]ATTGTGGTTGCTGTT	4703
rs368075131	snp	C/T	0.00015265	0.00873508	synonymous-codon	NEB	GRCh38.p7	2:151727880	AGATGTCCTTGTTGT[C/T]GTAGTCTCATAAATT	4703
rs368091868	snp	C/T	1.80922e-05	0.00300762	missense	NEB	GRCh38.p7	2:151682750	TTCATCCAGCTATTG[C/T]AGTCAGCTTTGTATT	4703
rs368108960	in-del	-/AAAG	0.0111196	0.0737302	intron-variant	NEB	GRCh38.p7	2:151641739	CCATATTTTGGAAAT[-/AAAG]AAAAAAATCTAGAGT	4703
rs368120887	snp	C/T	3.3345e-05	0.00408306	missense	NEB	GRCh38.p7	2:151665377	TAAGTGCCTGTTCCA[C/T]TGTGTCCATGGCGTA	4703
rs368124260	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151704423	GCTTTGTTTACCTAA[G/T]CAAGCCTGGGCAATG	4703
rs368125758	snp	C/G	5.18435e-05	0.00509108	intron-variant	NEB, RIF1	GRCh38.p7	2:151492367	GGCAGCCAGCCAATC[C/G]TAAAGAATTCCTGAC	4703
rs368135069	snp	C/T	0.00438332	0.0466095	intron-variant	NEB, RIF1	GRCh38.p7	2:151500644	TCCTGTTGCCTAGGC[C/T]GGAGTACAGTGGCAC	4703
rs368135985	snp	A/C	3.37319e-05	0.00410668	intron-variant	NEB, RIF1	GRCh38.p7	2:151527622	GGAATCACTTGATTC[A/C]GTAGGCTAAATTCAT	4703
rs368136951	snp	A/C/T	0.000132563	0.00814036	synonymous-codon	NEB	GRCh38.p7	2:151671131	CTTCCTCTCATTTAA[A/C/T]GCATCGCCTGCTTTC	4703
rs368146492	snp	A/G	3.79442e-05	0.00435553	intron-variant	NEB	GRCh38.p7	2:151688413	TGAAAAACAAAGGAT[A/G]TTTGAACGGTTCAGG	4703
rs368148074	snp	A/G	3.31378e-05	0.00407036	missense, intron-variant	NEB	GRCh38.p7	2:151644485	CACTGGCAATTTCCC[A/G]GGAGGCTTTTGCTGC	4703
rs368148266	snp	A/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151533052	TGTAGTGATAATTGA[A/T]CAAGAGACACATTAG	4703
rs368150737	snp	C/T	0.000149543	0.00864575	missense	NEB	GRCh38.p7	2:151696662	TGTTTGGAATTGACT[C/T]GGGCTTGTAGCAGAA	4703
rs368150913	in-del	-/GTTT			intron-variant	NEB, RIF1	GRCh38.p7	2:151486899	AGCATTTGTTTGTTT[-/GTTT]TAATTCACCAGAAGA	4703
rs368155040	snp	C/T	4.96792e-05	0.00498368	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151640484	CTTCTTGGCCAGCAC[C/T]ACCCCCAGCATGTCC	4703
rs368162542	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151701542	TCGCCACAATTTCAG[A/C]TCCTGTTATTGGTCT	4703
rs368162982	snp	A/T	1.6591e-05	0.00288015	missense, intron-variant	NEB	GRCh38.p7	2:151612225	CTTTGCTAGGACAAT[A/T]TCCGGAGTGTCGGTA	4703
rs368165645	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151719735	AATACAAAAATTAGC[C/T]GGGTGTGGTGGTGTG	4703
rs368167657	snp	A/G	1.65737e-05	0.00287864	missense	NEB	GRCh38.p7	2:151576240	TCACCACAGGCGTCC[A/G]ATAGACACTGTCACA	4703
rs368167929	snp	C/G	1.65734e-05	0.00287862	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151485809	CCGGTCCTGCCAGTC[C/G]TCTGCACAGTGCCAT	4703
rs368180456	snp	A/G	3.43737e-05	0.00414556	missense	NEB	GRCh38.p7	2:151655323	TATCTGGTGTATCAG[A/G]CATCACATGAATCTT	4703
rs368188014	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151660727	AAAGCAGCCAGAGAC[C/G]ACACGCCAACAAACA	4703
rs368196453	snp	C/G	0.000167986	0.00916324	missense	NEB	GRCh38.p7	2:151717427	TTACCTTGCTCACTT[C/G]ATTGGTTACTTTCTT	4703
rs368202765	snp	C/T	4.97047e-05	0.00498496	missense, intron-variant	NEB	GRCh38.p7	2:151627543	TCTGGAGGTCATAGG[C/T]CTGCCGAGCATGGAT	4703
rs368206682	snp	G/T	4.96956e-05	0.00498451	missense	NEB	GRCh38.p7	2:151568362	GTGTGCAGCAGGGGG[G/T]TTTCTGTGAGGGTGT	4703
rs368215104	snp	A/C	0.000157988	0.00888644	missense	NEB	GRCh38.p7	2:151671065	AGCCAACACCATGCC[A/C]ATGGAATCAGGCACA	4703
rs368217121	snp	C/T	0.000364263	0.0134907	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151640550	GTCCTTCTTGTACTC[C/T]CTGTCACTCTGGATC	4703
rs368224713	snp	C/T	8.27917e-05	0.00643343	missense, intron-variant	NEB	GRCh38.p7	2:151627608	TGCAGGTAGTTCTTG[C/T]AGTCCACATCGCTGA	4703
rs368230090	snp	A/G	0.000132705	0.00814463	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151612237	AATTTCCGGAGTGTC[A/G]GTAATGCATGTGAAT	4703
rs368232288	snp	A/G	0.000215276	0.0103726	missense, intron-variant	NEB	GRCh38.p7	2:151644078	CATCTTCAATGTTCC[A/G]GGCACCAATGTGGTG	4703
rs368240939	snp	C/T	2.23952e-05	0.0033462	missense	NEB	GRCh38.p7	2:151560692	TCCCAGGCCTCCTTG[C/T]ACAGGTTCTGCAGGA	4703
rs368242921	snp	A/G	0.000120338	0.00775595	intron-variant	NEB	GRCh38.p7	2:151547558	AAAAAATACCCCAAA[A/G]CATATGTATTAGAGA	4703
rs368244387	snp	C/G	1.8675e-05	0.00305568	missense	NEB	GRCh38.p7	2:151655364	TTATTCCAATCAATG[C/G]TGTATAAATGCTAGG	4703
rs368268273	snp	G/T	0.00010843	0.0073623	missense	NEB	GRCh38.p7	2:151690735	CACTTACATCACTAA[G/T]CTGTTTCGTGTTGAG	4703
rs368270996	snp	A/G	3.33706e-05	0.00408463	missense	NEB	GRCh38.p7	2:151665397	TCCATGGCGTAAGTG[A/G]ACTTCAGCTTCTCGG	4703
rs368290448	snp	C/G	0.000169985	0.00921758	intron-variant	NEB, RIF1	GRCh38.p7	2:151496251	TAAAATCAGTAAGTA[C/G]TTTTTTTCTTTTCTC	4703
rs368298310	snp	C/G/T	0.00010195	0.00713907	intron-variant	NEB	GRCh38.p7	2:151642899	AAAACATGACTGGTA[C/G/T]AGGCCAGTAATAAAT	4703
rs368298970	snp	A/G	2.44144e-05	0.00349379	intron-variant	NEB, RIF1	GRCh38.p7	2:151516570	GTATTTCACCTGGTG[A/G]TAGAAAGCCATGTTA	4703
rs368302286	snp	A/T	0.000563436	0.016775	missense	NEB	GRCh38.p7	2:151656267	GATGTTGGCTTGGGC[A/T]TCCTTTGCAGCCGTG	4703
rs368312506	snp	C/T	1.92354e-05	0.00310118	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151616017	ATCACTAGCAATATC[C/T]CTTGAAGCCTTGGCT	4703
rs368315700	snp	A/G	8.25764e-05	0.00642506	synonymous-codon	NEB	GRCh38.p7	2:151570123	GGCCTGAATCACATC[A/G]TTCTGGTCGGGCATG	4703
rs368315910	snp	A/G	8.28494e-05	0.00643567	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151529256	GCTTTGATATGAACA[A/G]CATCTGGCTCAATGG	4703
rs368328496	snp	A/G	6.62987e-05	0.00575717	synonymous-codon	NEB	GRCh38.p7	2:151548338	GTTGACTCTCCGGAC[A/G]TGGACAAATGGAACA	4703
rs368328716	snp	C/T	9.93986e-05	0.00704907	missense, intron-variant	NEB	GRCh38.p7	2:151610563	TTTTGATGGAAATAG[C/T]ATCTGCTCTCAGATC	4703
rs368334428	snp	A/C	3.46308e-05	0.00416104	intron-variant	NEB	GRCh38.p7	2:151538014	AGCTGTAAGTCTTAC[A/C]CAAAGTTAATGTAAA	4703
rs368346105	snp	C/T	0.000132657	0.00814314	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151485923	TAGTCATACATGGCA[C/T]GGAAGATTTTCTATT	4703
rs368353531	snp	C/T	5.0109e-05	0.0050052	intron-variant	NEB, RIF1	GRCh38.p7	2:151503336	GTTTCTTATATGATA[C/T]ATTTGTAAATACCGA	4703
rs368360859	snp	A/G/T	3.27295e-05	0.0040452	intron-variant	NEB	GRCh38.p7	2:151576113	TTCTCATCTATTTAT[A/G/T]GCATTAATTCAATTT	4703
rs368371414	snp	C/T	0.000332287	0.0128854	synonymous-codon	NEB	GRCh38.p7	2:151663695	ACTGAGCATGTCCAC[C/T]GGGGTGTGGAAGGAG	4703
rs368373064	snp	A/G	4.96857e-05	0.00498401	missense, intron-variant	NEB	GRCh38.p7	2:151640008	ACATCCAAAGAGCCA[A/G]TGGACACCCAGCCAA	4703
rs368377514	snp	C/G/T	3.38028e-05	0.00411102	missense	NEB	GRCh38.p7	2:151678141	TGAAGACTTTGGAAG[C/G/T]CAACCATTTTCCCTT	4703
rs368377930	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151584173	TCTATGAGGTAGATA[C/T]TATTATTAACATATA	4703
rs368383341	snp	A/G	0.00013271	0.00814476	NEB	2	allele_origin=G(germline)/A(germline)	2:151609892	CATGCAGGTAATTGC[A/G]ATAATCAATGTCAGT	4703
rs368398931	snp	A/C	0.00279162	0.0372561	upstream-variant-2KB	NEB	GRCh38.p7	2:151735359	TTTTCTTAAAACTTG[A/C]CTGATGTCTTTCTTG	4703
rs368399531	snp	C/T	1.68806e-05	0.00290517	missense	NEB	GRCh38.p7	2:151551824	CTCTGACACTGTGCA[C/T]ATAGTCATAGTGGTA	4703
rs368426954	snp	G/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151713446	TGGAAATCTTTCCAA[G/T]TCTATGTGATGGAAG	4703
rs368471624	snp	C/G	0.000115953	0.00761333	missense, intron-variant	NEB	GRCh38.p7	2:151650705	TCTTGGCCAGTACCA[C/G]TCCCAACATGTCCAC	4703
rs368475840	snp	C/T	0.000329946	0.0128399	intron-variant	NEB	GRCh38.p7	2:151565627	AGAAACGGAGACAAT[C/T]AAGACAGGTCTACCA	4703
rs368484176	snp	C/T	6.76521e-05	0.00581562	missense	NEB	GRCh38.p7	2:151553857	CTGTGACTTTCCTGA[C/T]GTGATCATTGACTTG	4703
rs368489561	snp	C/T	1.69691e-05	0.00291278	missense	NEB	GRCh38.p7	2:151541452	CTGAGCTTACCTGAC[C/T]CTGAAGCTTCTGCCC	4703
rs368494039	snp	C/T	0.000159987	0.00894248	missense	NEB	GRCh38.p7	2:151666256	GTGTGGTACTTGGTC[C/T]TGCTGGCTTCATAGC	4703
rs368498883	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151655018	TTTCAACAATTTTCT[A/G]TTGATTTCCTGCTTG	4703
rs368500993	snp	A/C/G	0.000151043	0.00868923	synonymous-codon	NEB	GRCh38.p7	2:151717500	AGCTTGCTGTTCAGC[A/C/G]AGACCTTTTTTGTAG	4703
rs368505253	snp	C/G	1.68746e-05	0.00290466	intron-variant	NEB, RIF1	GRCh38.p7	2:151519800	ACATCCAAATTATTC[C/G]TGGACATCAATCAAT	4703
rs368507593	snp	A/G	0.000163987	0.00905353	missense	NEB	GRCh38.p7	2:151690755	TTCGTGTTGAGCTGG[A/G]CTTGCAACAGTACAG	4703
rs368526624	snp	C/T	4.98434e-05	0.00499192	intron-variant	NEB	GRCh38.p7	2:151541559	TAGACCAGCTAGACA[C/T]AAACCAAGTTATCAC	4703
rs368569756	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151712562	GTCAGGGTGGAGATC[A/G]AGCTCTCACAATCCA	4703
rs368577765	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151676498	TTAAACATATTCAAC[A/G]TCTCTTCTTACCTAC	4703
rs368583298	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151733343	TTAAAATACAAGTAT[A/G]AACAGCAGAAGCTTC	4703
rs368585998	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151687594	CCCAAGGCCACCCTG[C/T]CCAGGTCCCCAGGTC	4703
rs368590269	snp	A/G	0.00517822	0.0506191	intron-variant	NEB	GRCh38.p7	2:151665596	GGCTTGTGTTTCTTT[A/G]GCTATGTGATTTACT	4703
rs368600988	snp	C/T	3.32535e-05	0.00407746	intron-variant	NEB	GRCh38.p7	2:151694287	GCAACTTTGTGGCCA[C/T]GTCTGAAAATAGGGG	4703
rs368614143	snp	A/C	7.08818e-05	0.0059528	intron-variant	NEB	GRCh38.p7	2:151724406	GGCTTGAGGTCTCAC[A/C]CAAAGGCATGAGGAT	4703
rs368625295	snp	A/G	0.000317835	0.0126022	synonymous-codon	NEB	GRCh38.p7	2:151679721	CACAGCTGGACTTAC[A/G]TCACTCGCCGCCTGC	4703
rs368626849	snp	C/T	1.65745e-05	0.00287871	missense	NEB	GRCh38.p7	2:151656400	ACTAATTTGGGATCA[C/T]CCTCGAGACTGCGGA	4703
rs368626961	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151521417	TCTCAACATAAAGAA[A/G]TGGAAGGCCTGCTAA	4703
rs368636884	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151609365	ATTGATCACAGAAGT[C/T]ACTTGTAAAAACATA	4703
rs368637389	snp	C/T	0.000149055	0.00863164	missense, intron-variant	NEB	GRCh38.p7	2:151643185	TGTTTTTTGCCAAAA[C/T]CATTGGTATGGAATC	4703
rs368642083	snp	C/T	5.49828e-05	0.00524294	missense	NEB	GRCh38.p7	2:151682684	AGGATGTCTGAAGCT[C/T]GCTTTGCCTTTTCCA	4703
rs368644406	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151561846	CTAAGGTACAGATGC[C/T]TGAGAGTAGTTCACT	4703
rs368668412	snp	A/C	6.05382e-05	0.0055014	intron-variant	NEB	GRCh38.p7	2:151706831	AAGGAGAAAATTTTC[A/C]TCTCTTTTGCAGCTA	4703
rs368671999	snp	C/T	0.000730342	0.0190955	intron-variant	NEB	GRCh38.p7	2:151687590	TGTCCCCAAGGCCAC[C/T]CTGTCCAGGTCCCCA	4703
rs368678889	snp	C/T	0.00318978	0.0398085	intron-variant	NEB	GRCh38.p7	2:151733660	TCTTAGGCTTCAAAT[C/T]GGAACCCATAAAAAT	4703
rs368682145	snp	C/T	0.000314671	0.0125394	synonymous-codon	NEB	GRCh38.p7	2:151674546	CAGCACATTGTTGCC[C/T]TTGGCTATTAAGTCA	4703
rs368694337	snp	A/G	4.80296e-05	0.00490025	synonymous-codon	NEB	GRCh38.p7	2:151664501	AGTGCAAGCACTTAC[A/G]TCACTGGCAATGTCT	4703
rs368695432	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151517052	TTATTTATAAGTAAA[C/T]AACTCTATGTGGGTC	4703
rs368703295	snp	C/T	0.000163987	0.00905354	intron-variant	NEB	GRCh38.p7	2:151640341	TGCACGTTATTATGA[C/T]TCTCAGTACTCACAT	4703
rs368710945	snp	C/T	1.85955e-05	0.00304916	intron-variant	NEB	GRCh38.p7	2:151653945	CGACATTAAGTCACC[C/T]GATTCAGATAAAAAT	4703
rs368718211	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151628077	ATGGGAATAGTCCAG[G/T]GGGAAGACAGGCCAA	4703
rs368719373	snp	C/T	0.000430592	0.0146666	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151627080	AAATTTCAGCTTGTC[C/T]GGAGGCTGGCGGTAG	4703
rs368738886	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151564871	CACCAGCTGAATAAA[C/T]GCTATTTGCCTTGAA	4703
rs368764053	snp	C/T	1.65877e-05	0.00287986	intron-variant	NEB, RIF1	GRCh38.p7	2:151505613	GGTATTATTACATGC[C/T]GGACTGTTATTCTTC	4703
rs368770648	snp	A/G	1.85451e-05	0.00304503	intron-variant	NEB, RIF1	GRCh38.p7	2:151525315	GAGTAGAGGAAGCTG[A/G]GAACAGAGTTGGTTT	4703
rs368774294	snp	A/G	0.000165986	0.00910855	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151506262	TTTATATAAAACCTG[A/G]GCATTCAGAATCAGG	4703
rs368776493	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151691776	CTTCTAATCACTAGA[A/T]ATTAGCATGTAAACT	4703
rs368778921	in-del	-/TCT			intron-variant	NEB	GRCh38.p7	2:151573908	CTTAAAATGACTTCT[-/TCT]GCAAATAATGATAAT	4703
rs368799447	snp	A/C	1.82657e-05	0.003022	intron-variant	NEB	GRCh38.p7	2:151609769	AATGAACAAATCTAC[A/C]TCTTCCCCTTCCCCC	4703
rs368800654	snp	C/T	1.65999e-05	0.00288091	missense, intron-variant	NEB	GRCh38.p7	2:151640653	TGCTTACGATAGCCT[C/T]CTTTGTACTTGAACT	4703
rs368803600	snp	A/G	0.000181665	0.00952887	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151620919	TTGATCAGCTCTTAC[A/G]TCACTGGCAATATCC	4703
rs368804328	snp	C/T	0.00557542	0.0525036	intron-variant	NEB	GRCh38.p7	2:151702859	ATTGGAGCATTAAGT[C/T]CATTTACATTTAAAG	4703
rs368821800	snp	C/T	0.000387406	0.0139123	intron-variant	NEB	GRCh38.p7	2:151696615	TCATAATTGGGTGTC[C/T]TGAGTAGTTAGAGGA	4703
rs368826289	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151552248	AATGGGAGGCTCAGA[C/T]GGATTAAGTGCTTTT	4703
rs368831828	snp	C/T	1.65666e-05	0.00287802	intron-variant	NEB, RIF1	GRCh38.p7	2:151518285	CTGTGGATGAATGTG[C/T]GCCAGAGGAAAAATC	4703
rs368837832	snp	A/G	0.104149	0.203046	intron-variant	NEB	GRCh38.p7	2:151606120	CCACCATGCCCGACA[A/G]GTAGCATAATTATTT	4703
rs368842783	snp	C/T	9.17305e-05	0.00677177	missense, intron-variant	NEB	GRCh38.p7	2:151625567	ATTTTGTCTTGCCAA[C/T]ATGATTTCAGGTGTA	4703
rs368857335	in-del	-/GTCT			intron-variant	NEB	GRCh38.p7	2:151625332	TTTTTGTGTCTGTCT[-/GTCT]ATCTGTCTGTCTAAT	4703
rs368866814	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151719886	AGTGAGACCCTGTCT[A/C]AAAAAAAAAAAAAAA	4703
rs368876005	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151607153	GCCATCTGGATGTAA[A/T]TAGAAATGGTCTTTT	4703
rs368876425	snp	A/C/G/T	8.13531e-05	0.00637742	synonymous-codon	NEB	GRCh38.p7	2:151562671	TTCTTCCAGAAGAGA[A/C/G/T]GTCCACTGGTGGAAA	4703
rs368883773	snp	C/G/T	9.11006e-05	0.0067486	missense	NEB	GRCh38.p7	2:151549645	ACTCACATAACTGCT[C/G/T]ATGTAACGGGTGTCC	4703
rs368886308	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151578952	CTGGGTGTGGTGCAC[A/G]TGCCTGTAATCCCAG	4703
rs368887173	snp	A/C/T	0.000122327	0.00781986	synonymous-codon	NEB	GRCh38.p7	2:151535733	GAAATGCCTATTGAT[A/C/T]GGAGAGTCGGCAACA	4703
rs368898214	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151695292	TGGCTAAAAGATCTA[A/C]CATTAAAATTTGCAA	4703
rs368912483	snp	A/G	0.000142498	0.00843972	missense	NEB	GRCh38.p7	2:151567427	TCATCTCTCATCGTC[A/G]GGACACCAACATAAT	4703
rs368915047	snp	C/T	0.000506009	0.0158981	missense, intron-variant	NEB	GRCh38.p7	2:151617467	GCTTCAGTATATAAG[C/T]GCTACAAAAAAAAAA	4703
rs368928126	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151493258	TTTTAAAATTTTAGT[A/G]TGTTTTTCAGTTGAA	4703
rs368938540	snp	C/T	0.00438332	0.0466095	intron-variant	NEB, RIF1	GRCh38.p7	2:151527749	ATTTATGCAGCTAGT[C/T]ATCCACTCAGAGGTC	4703
rs368941494	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151641036	GGTTTTATATGCTCA[A/T]TGATCCAAAATTTCA	4703
rs368952983	snp	A/G	1.65784e-05	0.00287905	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151529280	TCAATGGTGCAGTTG[A/G]ATTTATTTCTTTGGT	4703
rs368953684	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151530627	GATATGTTTAAGCCA[C/T]GTGGAGACCCATCTG	4703
rs368954128	snp	C/T	0.000512241	0.0159956	intron-variant	NEB	GRCh38.p7	2:151616135	GAAAGTCATTACTCA[C/T]TTACTCCTTCCATAA	4703
rs368955312	snp	A/G	2.98878e-05	0.00386562	intron-variant	NEB, RIF1	GRCh38.p7	2:151496402	TCCAGAAAAACAACC[A/G]TGAGTAACATTTCAT	4703
rs368956947	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151701297	GATTTTTGCATCAAT[A/G]TTCATCAAGGATATT	4703
rs368965372	snp	A/G	9.39541e-05	0.00685334	missense, intron-variant	NEB	GRCh38.p7	2:151639384	CTTCTGTGTATAAAC[A/G]CTATCAAAAAAAATA	4703
rs368967111	snp	A/G	1.98371e-05	0.00314931	missense	NEB	GRCh38.p7	2:151562645	GCGTTTCGGACGCGT[A/G]TAACATTGGGTTCTT	4703
rs368972405	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151659264	TATCAATATTTCATG[C/T]ATTTTTATTAGCTAG	4703
rs368977093	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151679641	GACTGCATGCATGGA[A/G]ACTTTTGGGTCATCG	4703
rs368988777	snp	A/G	1.66197e-05	0.00288263	intron-variant	NEB, RIF1	GRCh38.p7	2:151518436	TACTGAGGGGAAGGC[A/G]GCAAAAAAGGCACAT	4703
rs368998033	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151684644	ATGCTCTTATAGAAC[C/T]ACAAGGGTCGTTTGC	4703
rs369010036	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151641246	GTCATATTGTATATG[A/G]GTTTGTGCCTGCTCT	4703
rs369014813	snp	C/G	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151620028	AAGAGTCCAATTACA[C/G]TAATAAACCATGATG	4703
rs369024842	snp	C/T	0.000167986	0.00916322	intron-variant	NEB	GRCh38.p7	2:151561137	ACAATAGGTTATTCA[C/T]CTCTGTTGTTAGAAA	4703
rs369038670	snp	A/G	3.96503e-05	0.00445237	intron-variant	NEB	GRCh38.p7	2:151630707	GCACCACAGATTTTT[A/G]CTCCTACCTCACTGT	4703
rs369040645	snp	A/C/T	0.000116667	0.00763689	intron-variant	NEB	GRCh38.p7	2:151610502	CCACAGAGAGTTAGA[A/C/T]GGAAGGTACTCACGT	4703
rs369042477	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151497281	AGAGTTATCCATGTT[A/G]TTTTTTTTTTTCCTT	4703
rs369046108	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151701991	CTTTCCTGCTTTCTC[C/T]TGTGGGCATTTAGTG	4703
rs369051192	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151514041	CAGTGTAGTGTTTTC[A/G]TGTAGATGAGCACAC	4703
rs369054525	snp	A/G	4.97113e-05	0.00498529	missense	NEB	GRCh38.p7	2:151554974	CACCGTGCTGTGTTC[A/G]GATCATCGTCAACAC	4703
rs369065019	in-del	-/AG/AGAGAGAG/G/GAGAG	0.2688	0.249292	NEB	2	allele_origin=G(germline)/(germline)	2:151617487	AAAAAAAAAAAAAAA[-/AG/AGAGAGAG/G/GAGAG]AGAGAGAGAGAGAGA	4703
rs369065324	snp	A/G	3.41303e-05	0.00413086	missense	NEB	GRCh38.p7	2:151570311	CAGCTATGAGGGCCC[A/G]GCGGATCTTGTTGTC	4703
rs369069068	snp	C/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151511089	AGTGACGTGATCCCA[C/G]ACTGGGATAGGTCCA	4703
rs369071102	snp	A/G	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151675863	CCTCATAATGTAGAG[A/G]TGCTTATACATGAAT	4703
rs369083039	snp	A/G	1.69183e-05	0.00290841	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151493408	TCTGGAGTAACAGGT[A/G]TCGGAGTTGCTTTTC	4703
rs369085018	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151555216	AGATACAGCAGTAGC[A/G]CCTGCCATGGGGTTA	4703
rs369098763	snp	C/T	3.31203e-05	0.00406928	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151514385	TCCATTTCAGTGAGG[C/T]CCTTCCCACGGATGC	4703
rs369105505	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151504182	TTAAATGGATGGATT[C/T]CCTGGTGTATTAGTG	4703
rs369125377	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151578131	CTTAAGGGAACCAAG[A/G]TCAGATAATTTTTAA	4703
rs369143071	snp	C/G	6.21601e-05	0.0055746	missense	NEB	GRCh38.p7	2:151562679	GAAGAGACGTCCACT[C/G]GTGGAAATAGTGTCG	4703
rs369147939	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151601054	TGTACTTCTTATTAC[G/T]TTAAATCAAATTAAT	4703
rs369153778	snp	G/T	0.000368528	0.0135694	missense	NEB	GRCh38.p7	2:151706988	TTTCATAGTCTTCTT[G/T]GTATTTTACCTGTAG	4703
rs369174368	snp	C/G/T	4.58747e-05	0.00478908	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151491703	ATCATGTGTAAGCTT[C/G/T]GGGACTGGATGTTGT	4703
rs369179720	in-del	-/CTCT			intron-variant	NEB	GRCh38.p7	2:151690987	TCTCTCTCTCTCTCT[-/CTCT]TTTTCCTTTAATCCC	4703
rs369183371	snp	A/G	0.000293915	0.012119	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151531099	TTCCAATTTATAAAG[A/G]ATCTGAAAGATCAAA	4703
rs369188503	snp	A/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151531902	TGTATTTGATCTAAA[A/T]TGTGGAAGAGAAGAA	4703
rs369195516	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151571917	TATCCTTGTAAGCAT[A/G]GACAGGTTTTATATG	4703
rs369198856	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151576405	GTTTTGTTGTGTATG[C/T]GTGTGGTAAAATAAG	4703
rs369208403	snp	C/G	0.000165986	0.00910855	intron-variant	NEB, RIF1	GRCh38.p7	2:151492071	TCACTTAAAGTTAAT[C/G]CCCTCCCCCAACCCA	4703
rs369215974	snp	C/T	0.000148064	0.00860291	missense	NEB	GRCh38.p7	2:151657991	GACTTACATCACTTG[C/T]AATATCTCTGGAAGC	4703
rs369220518	snp	G/T	3.46614e-05	0.00416287	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151526959	GGGCGAGCACCGTGT[G/T]TTTGTCATCAGTGAC	4703
rs369222043	snp	A/T	1.66557e-05	0.00288575	synonymous-codon	NEB	GRCh38.p7	2:151667843	TTTTGCAGCAACAAT[A/T]GGGATGGCATCTGGT	4703
rs369224273	snp	C/T	1.65765e-05	0.00287888	missense, intron-variant	NEB	GRCh38.p7	2:151643290	TATTTTTCTCATCCT[C/T]GAGAGAACCACTAGT	4703
rs369229042	in-del	-/A	0	0	intron-variant	NEB, RIF1	GRCh38.p7	2:151513711	AAAAGAAAAAAAAAA[-/A]GGTACCTAAATGCTA	4703
rs369262243	snp	C/T	3.79802e-05	0.0043576	missense	NEB	GRCh38.p7	2:151691874	CTTACATCTTTACAC[C/T]GGTCCAGCTTCTTGA	4703
rs369273788	snp	A/G	1.79829e-05	0.00299852	missense	NEB	GRCh38.p7	2:151684881	TCAACGTCGCTGGCA[A/G]TTGCCTGAGATTTCT	4703
rs369275207	snp	C/T	8.64367e-05	0.0065735	missense	NEB	GRCh38.p7	2:151664542	TTGCAGCCTTTATTG[C/T]AATGGCATCAGGCCT	4703
rs369276552	snp	C/T	8.32362e-05	0.00645067	intron-variant	NEB	GRCh38.p7	2:151717559	GTATTTTAAAAACGA[C/T]TATGCTTTCATCTTT	4703
rs369283016	snp	C/T	0.000198758	0.00996691	missense, intron-variant	NEB	GRCh38.p7	2:151640393	GCCGAGCATGGATGA[C/T]GTCGCTCTGGTCGGG	4703
rs369292364	snp	G/T	1.65663e-05	0.002878	missense	NEB	GRCh38.p7	2:151725521	TTGTGCTGGCGTATG[G/T]CTGTCCTTTTGTTTT	4703
rs369310946	in-del	-/C			intron-variant	NEB	GRCh38.p7	2:151673732	AAAATTTTTCTTTTT[-/C]TTTTTTTTTTTTTTT	4703
rs369321748	in-del	-/C	0.00557542	0.0525036	intron-variant	NEB	GRCh38.p7	2:151633066	GCTAGTGCTTTAATT[-/C]CTTCAAAGTTTATAA	4703
rs369331223	snp	C/G/T	4.97511e-05	0.00498733	intron-variant	NEB	GRCh38.p7	2:151697296	TGCAGCCATTGTATT[C/G/T]ATGCCCTGAGAAAAA	4703
rs369339460	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151488914	ATTTTGTATCTATTG[C/T]CATGCTAAATCCATA	4703
rs369352855	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151552583	TTAGAAAAGACTTGG[C/T]ACTGCCCAGTCTATG	4703
rs369373369	snp	G/T	1.6582e-05	0.00287936	missense	NEB	GRCh38.p7	2:151677972	CTTATAGTTGACATT[G/T]CTGACCACATCCTGG	4703
rs369374856	snp	A/G	1.65734e-05	0.00287862	missense	NEB	GRCh38.p7	2:151655888	GCTTCTTAAACTGGA[A/G]GTTGCTCGGGTGCTG	4703
rs369378749	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151649524	AGATTTCAGGGCACA[C/T]ACTTCAGTATTCTGT	4703
rs369384031	snp	A/T	9.95206e-05	0.0070534	intron-variant	NEB	GRCh38.p7	2:151729581	TCCTGCTTTAATGAG[A/T]ATGCAGTTTATGCAG	4703
rs369385033	snp	A/T	4.96808e-05	0.00498377	missense, intron-variant	NEB	GRCh38.p7	2:151627702	TCTTCCACTTCTCAA[A/T]GTCCTTCTTATACTC	4703
rs369400827	snp	A/G	2.67921e-05	0.00365996	synonymous-codon	NEB	GRCh38.p7	2:151568675	AACTCTGTCATCCAC[A/G]GGCGTAAAGTTGAGA	4703
rs369406950	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151645444	GTTTAAATAATGAAT[C/T]TTAAAAGCTTAAGTG	4703
rs369409568	snp	C/T	1.78928e-05	0.002991	intron-variant	NEB	GRCh38.p7	2:151697103	ATCCTGACCACTAGA[C/T]GCTATGGAAGGCAGT	4703
rs369413843	snp	C/T	3.10313e-05	0.00393887	intron-variant	NEB	GRCh38.p7	2:151684758	TTAAAAGAGGGGCTA[C/T]AGAAACCCTGGTTAC	4703
rs369413888	snp	A/G	0.000163986	0.00905352	synonymous-codon	NEB	GRCh38.p7	2:151655960	CCTTCTCCACTTCCA[A/G]AGAACCTGCTGGACT	4703
rs369420017	snp	C/T	4.97492e-05	0.0049872	intron-variant	NEB, RIF1	GRCh38.p7	2:151489926	CATGTTTGCACATAT[C/T]AAAAATTAAGAATAA	4703
rs369420467	snp	A/G	1.66087e-05	0.00288168	synonymous-codon	NEB	GRCh38.p7	2:151662324	CATGAAGTCAGCATA[A/G]TCAGCCTTGTACTGA	4703
rs369426786	snp	C/T	5.02651e-05	0.00501299	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151654022	TCTTGAAGCTTTAGC[C/T]AGCTGTACAGAAATT	4703
rs369428164	snp	A/G	1.77577e-05	0.00297969	synonymous-codon	NEB	GRCh38.p7	2:151552741	GACAAGCTTGTAGTC[A/G]TTCCTTGTTTTCAAC	4703
rs369429046	snp	A/G	8.28741e-05	0.00643663	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151614318	AGCCTGAATGACGTC[A/G]TTCTGATCAGGCAGG	4703
rs369431254	snp	C/G	6.63911e-05	0.00576118	intron-variant	NEB	GRCh38.p7	2:151694467	ACATGCCAGATTCCA[C/G]TCAAGAGGAAATGTC	4703
rs369433731	snp	A/C/G	0.000199002	0.00997331	synonymous-codon	NEB	GRCh38.p7	2:151569286	ACTGAAGATGTCCGC[A/C/G]GCATGTTTGGCATGA	4703
rs369436489	snp	C/T	9.93657e-05	0.00704791	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151524393	TGGCTGCCTTCCTTG[C/T]GGTGCTTGGCTCTGT	4703
rs369441230	snp	A/G	0.000257107	0.0113352	intron-variant	NEB	GRCh38.p7	2:151691976	TAACTTTTCTATAAT[A/G]AGAAAAACCAAAAAT	4703
rs369449701	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151611877	AGTGGCCTGAATCTG[C/G]TCTGCCTAGGAGAAT	4703
rs369449864	snp	A/C	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151693425	TTCTCCCGCCTCCCC[A/C]ACCCCCAGCCTCCAA	4703
rs369456343	snp	C/G/T	0.000132586	0.00814098	missense, intron-variant	NEB	GRCh38.p7	2:151650833	TCATCTTGCAGACTC[C/G/T]GGAATCCAACATGGT	4703
rs369465041	snp	A/G	0.000169986	0.00921758	intron-variant	NEB	GRCh38.p7	2:151665569	AAAAAATTTCATTTC[A/G]GAAAGAGTCAGGGCT	4703
rs369467210	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151648139	ATGCACACACACATA[C/T]ACACATATGTGAATT	4703
rs369496057	snp	C/T	6.62636e-05	0.00575564	missense, intron-variant	NEB	GRCh38.p7	2:151644530	CATCAACAGGAAGAT[C/T]GTAACCTTTTCTCTT	4703
rs369504639	snp	G/T	5.01027e-05	0.00500488	intron-variant	NEB, RIF1	GRCh38.p7	2:151490561	TAGCAAACATGAAAT[G/T]TCTATGGTAGTAATG	4703
rs369508429	snp	A/G	6.62998e-05	0.00575721	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151619670	CTGCACTTTGGCAAT[A/G]TGGAGGGACCACATT	4703
rs369514902	snp	G/T			intron-variant, utr-variant-3-prime, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151497999	CAATCACATGAGGAT[G/T]TGAGACTGTTAGAAC	4703
rs369514998	snp	C/T	0.000116249	0.00762306	missense, nc-transcript-variant, intron-variant	NEB, RIF1	GRCh38.p7	2:151506940	TGATTTTCTTTTACA[C/T]GCAGTATTTCTGGCG	4703
rs369515076	snp	A/G	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151514996	TATCTCTCCATCTCA[A/G]GAAGAAAAAAAAAAC	4703
rs369521405	snp	A/G	0.000165986	0.00910854	intron-variant	NEB, RIF1	GRCh38.p7	2:151526282	AGGGGCAGGAAAAGG[A/G]GCATTTCTTTAGCTC	4703
rs369523677	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151705853	ATATGCTCTCACTTA[C/T]AAGTGGAAGCTAAGC	4703
rs369529666	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151553017	CTTTCTTACTGAAAT[C/T]CTCATTACAGTATTT	4703
rs369533357	snp	C/T	2.40532e-05	0.00346786	missense	NEB	GRCh38.p7	2:151665515	TCCCTTTCATCCAAT[C/T]GGTGAAGTCAGATTT	4703
rs369534205	snp	C/T	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151562544	GCATGGCAGCCAGGG[C/T]TGGGGGGTAGCCAAG	4703
rs369556101	snp	A/G	0.00017916	0.00946297	intron-variant	NEB	GRCh38.p7	2:151642542	AATCTTTGAGCCAAA[A/G]CTAAGGCAAATAACT	4703
rs369562967	snp	A/G	0.000161987	0.00899817	missense	NEB	GRCh38.p7	2:151549677	TGATGTGTTTGAAGT[A/G]AGGAGTGTCACCTGG	4703
rs369602540	snp	C/T	1.65993e-05	0.00288086	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151503414	CAGTGGTTGGAATGC[C/T]TGTTCCCAAGTTTTC	4703
rs369611234	snp	C/T	9.94299e-05	0.00705018	synonymous-codon	NEB	GRCh38.p7	2:151538197	TAGGGCATCTTTCAC[C/T]GTGTGGTATTTCCCT	4703
rs369626112	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151674110	ACATTTTATATAACA[C/T]CTTTTCAATCTTTTT	4703
rs369632989	snp	C/T	0.000160304	0.00895132	intron-variant	NEB	GRCh38.p7	2:151535813	AGAAAAAACAGAACA[C/T]GGTTACTTGACAGCA	4703
rs369636789	snp	C/T	8.31981e-05	0.0064492	intron-variant	NEB, RIF1	GRCh38.p7	2:151505440	GCAATTGAGAGATGG[C/T]CAGTCACACAAATGG	4703
rs369641020	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151706736	GGGACTCATGCCTTT[C/T]TGTGGTTACATAGTT	4703
rs369642754	snp	G/T	0.000165986	0.00910855	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151525171	AACTTACATCACTTT[G/T]CTTCTTGGCCACTTC	4703
rs369667745	snp	A/C	4.96841e-05	0.00498393	missense, intron-variant	NEB	GRCh38.p7	2:151633939	ATGGTGGCCAAGTTG[A/C]TTGCAGTAACCATCT	4703
rs369672584	in-del	-/CAA			intron-variant	NEB	GRCh38.p7	2:151688732	GTAAGAGATTAACAA[-/CAA]TAACTAATAAATAGA	4703
rs369688367	snp	C/T	4.96997e-05	0.00498472	synonymous-codon	NEB	GRCh38.p7	2:151576280	CTGGGCGTTTTTGAC[C/T]CTCAACACTTCAGGA	4703
rs369699291	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151492669	GGACCAGAAGGGCCC[A/G]CCAGTGGAAGAGAAA	4703
rs369707120	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151623717	GATAAATTCCAGAGG[A/G]AATCTGTTTTTCTTC	4703
rs369721821	snp	A/G	0.00557542	0.0525036	intron-variant	NEB	GRCh38.p7	2:151618875	TATTTCCATCTTCAA[A/G]AATCACAAAACTTCA	4703
rs369758648	snp	C/T	0.000117633	0.0076683	intron-variant	NEB, RIF1	GRCh38.p7	2:151526907	CATCATGGAAGGAAC[C/T]AGGTACTTACATCAC	4703
rs369765913	snp	C/T	0.000165986	0.00910854	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151519069	CAGCCTTGTATTTAA[C/T]CTGTGTGTTATGGGG	4703
rs369805203	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151577736	GGCACATGCCACCAC[A/G]CCAGGCTAATTTTTG	4703
rs369807844	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151492721	ATGAAACTCATTTTC[A/G]AAGAAGGGGCACGGT	4703
rs369843963	snp	A/G	1.65836e-05	0.0028795	intron-variant	NEB	GRCh38.p7	2:151729599	GCAGTTTATGCAGCT[A/G]TGGGCTGGGCCTTAC	4703
rs369875205	snp	C/T	3.9604e-05	0.00444977	missense	NEB	GRCh38.p7	2:151684794	TCGCTCTGCAGCGCA[C/T]ATGCCTTCTTGGCAA	4703
rs369888024	snp	A/G	1.81648e-05	0.00301365	intron-variant	NEB	GRCh38.p7	2:151725011	GGCATGTACATGTGA[A/G]TATATTAAGGAATTT	4703
rs369897667	snp	C/T	0.00515036	0.0504842	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151636257	CCTGGAGGCCTTGGC[C/T]GCCACGATGGGGATG	4703
rs369903833	snp	A/G/T	3.31528e-05	0.0040713	intron-variant	NEB	GRCh38.p7	2:151679900	CATACGCATCAGCCC[A/G/T]TGAGTCCACCCACGC	4703
rs369908508	snp	A/G	6.6443e-05	0.00576343	intron-variant	NEB	GRCh38.p7	2:151655782	CTAGCCTTTCCTCAC[A/G]TGGGAGCTGTGTGGA	4703
rs369912398	snp	G/T	0.000248614	0.0111465	intron-variant	NEB	GRCh38.p7	2:151677807	GGAGTGAGGGCCTAG[G/T]ACAGGGTTCTTTTCA	4703
rs369913099	snp	A/C	2.18926e-05	0.00330845	intron-variant	NEB	GRCh38.p7	2:151667949	TTATTATTTGACATC[A/C]TTAAAAGAGGAATGA	4703
rs369915027	snp	C/G	0.000164478	0.00906709	intron-variant	NEB	GRCh38.p7	2:151694633	CTTATAAAGATTCTG[C/G]ACAAAAAAATTCAGC	4703
rs369957704	snp	A/G	4.99172e-05	0.00499561	missense	NEB	GRCh38.p7	2:151697614	TAATTTATGCTCTTT[A/G]CTTTTGTCTTTTCAT	4703
rs369985728	snp	C/T	3.31214e-05	0.00406935	missense, intron-variant	NEB	GRCh38.p7	2:151631183	TTGGCCAGCACCTGC[C/T]CTAGAGAATCAGTCA	4703
rs369995092	snp	G/T			missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151518347	CTGTGGCCTCTTTTA[G/T]GTGAAGCTGCTCCAG	4703
rs369998169	snp	C/T	0.000161987	0.00899817	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151650826	TTTTGGGTCATCTTG[C/T]AGACTCCGGAATCCA	4703
rs369999168	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151557495	ACAACAGAAAAAGAG[A/G]GAATCCTCCCTAACT	4703
rs370000978	snp	A/G	0.000185925	0.00963993	missense	NEB	GRCh38.p7	2:151664802	GAGAGTAAAATATCC[A/G]GTGTGTCAGGCATGA	4703
rs370002963	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151513837	TCACCTTCGCTCTTC[C/T]GTGTGGTAGGATGAA	4703
rs370002964	snp	C/T	0.000157988	0.00888644	missense, intron-variant	NEB	GRCh38.p7	2:151640443	AGGTAGTTCTTGTAG[C/T]CCACATCGCTGACTA	4703
rs370016228	snp	C/T	9.0824e-05	0.00673823	intron-variant	NEB	GRCh38.p7	2:151551699	CAGAGGCTGATGGAA[C/T]GGATTTCTGCTGGGC	4703
rs370017162	in-del	-/AAGA			intron-variant	NEB, RIF1	GRCh38.p7	2:151501749	GCCTTCTCTCAAAGA[-/AAGA]CCAGAGTATCAAATA	4703
rs370036294	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151710410	CTCCCAGGATGACCA[A/G]CCAGCCATCCCTTCC	4703
rs370053963	snp	C/T	0.00046383	0.0152217	missense, intron-variant	NEB	GRCh38.p7	2:151627008	GGGGCTCACCTTGTT[C/T]ATATTGAGAGCATTG	4703
rs370064089	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151632535	ACAAAAAATTAGTGG[C/G]GCAGGGAGGCAGCAG	4703
rs370064863	snp	A/C/T	5.05165e-05	0.00502551	missense, stop-gained	NEB	GRCh38.p7	2:151669110	TGTGCTTCAGTTTCT[A/C/T]TCCCTCTACCTTGTA	4703
rs370068571	snp	A/G	4.98956e-05	0.00499453	missense, intron-variant	NEB	GRCh38.p7	2:151610077	ATGCTCTGGGCTCCA[A/G]TGTGGTGGCCTTTCT	4703
rs370068618	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151612589	GCCAATATTTACTGT[C/T]TTAAAGACTCATAAA	4703
rs370074798	snp	C/T	3.31175e-05	0.00406911	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151643920	GTCCACGTCGCTGAC[C/T]AAGGTCTGGCACTTC	4703
rs370082885	snp	A/G	1.65748e-05	0.00287874	missense	NEB	GRCh38.p7	2:151554941	CTTACATCGATGTTA[A/G]GCTTGCCAACTCGGA	4703
rs370086704	snp	C/T	0.00111478	0.0235828	intron-variant	NEB	GRCh38.p7	2:151568274	TTCCATTAAGGCCCT[C/T]CACTCGTACACAAAC	4703
rs370098540	snp	C/G	1.83478e-05	0.00302879	missense	NEB	GRCh38.p7	2:151545962	CTTTGTATTTGTCTC[C/G]CATCTTCCTTGCCTT	4703
rs370099071	snp	A/G	4.04032e-05	0.00449444	missense	NEB	GRCh38.p7	2:151547436	ATGCTTACATCACTG[A/G]TGATGTCTCCCACAT	4703
rs370108917	snp	A/G	0.000149381	0.00864108	missense, nc-transcript-variant, intron-variant	NEB, RIF1	GRCh38.p7	2:151506955	CGCAGTATTTCTGGC[A/G]TGTCTTGAACAACTG	4703
rs370126271	snp	A/C			synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151531837	ACGCAGGTGTTCTGG[A/C]GTATCCACAATTGAG	4703
rs370161504	snp	A/C	9.97191e-05	0.00706043	missense, intron-variant	NEB	GRCh38.p7	2:151618438	TCAATCGGAACCCAG[A/C]CAATGCCTTTCATCC	4703
rs370165599	snp	A/G	0.000167986	0.00916323	intron-variant	NEB	GRCh38.p7	2:151575684	AAAAGAGAGTCTGTT[A/G]TAGTACTTACATTGC	4703
rs370172690	snp	C/T	0.000132721	0.0081451	missense	NEB	GRCh38.p7	2:151663757	CCCGGTCTGACTGCA[C/T]CTTGGCCACTTGCAT	4703
rs370176216	snp	A/G	0.000264997	0.0115078	synonymous-codon	NEB	GRCh38.p7	2:151687467	CAGCATCTTTGGATC[A/G]TCATTAATGCTGAGG	4703
rs370176412	snp	C/T	0.000161987	0.00899819	missense, intron-variant	NEB	GRCh38.p7	2:151643856	GCCGAGCATGGATGA[C/T]ATCGCTCTGGTCGGG	4703
rs370178501	snp	C/T	0.000132705	0.00814463	intron-variant	NEB	GRCh38.p7	2:151563581	ATGGGGCACAAATCC[C/T]GTGTTAAAGTGGACA	4703
rs370178599	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151701345	TTTGGTTGTGTCTCT[C/G]CCTGGCTTTGGTATC	4703
rs370178670	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151528961	TTTCTCAGCCACCCA[C/T]CGCAAAAGCTGAGTG	4703
rs370185522	snp	C/T	3.34297e-05	0.00408824	synonymous-codon	NEB	GRCh38.p7	2:151551756	ACTCTGGAGCTTGTA[C/T]GCATGAAGGGCCCGG	4703
rs370189384	snp	A/G	3.31422e-05	0.00407063	missense, intron-variant	NEB	GRCh38.p7	2:151618364	TTTCTGGACGCTGAC[A/G]GTAGATAGTATCACT	4703
rs370198621	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151701781	ATTAGTCTTGCTAGC[A/G]GTCTATCTATTTTGT	4703
rs370199118	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151617658	TGTTAAAGGACTTAT[C/T]GGTTATGAAAAGTAT	4703
rs370200484	snp	A/G	6.77484e-05	0.00581976	intron-variant	NEB	GRCh38.p7	2:151562811	TTCTGTAGTTCAACT[A/G]ATATGTTTTAAAGAC	4703
rs370206339	snp	A/T	0.000182247	0.00954414	missense	NEB	GRCh38.p7	2:151562158	GAGGATTTGGGGTGT[A/T]TCCCAAACGTAGCAA	4703
rs370211010	snp	A/T	1.66994e-05	0.00288953	missense	NEB	GRCh38.p7	2:151537163	TTGTTCTTTTCAGCC[A/T]GAGTGAAATCAGGGG	4703
rs370252074	snp	A/G	1.65658e-05	0.00287795	missense	NEB	GRCh38.p7	2:151679962	CCTGGATGAACTGGG[A/G]CAGGTCTGGTGGCAG	4703
rs370262770	snp	C/T	0.000167986	0.00916323	intron-variant	NEB, RIF1	GRCh38.p7	2:151494137	TTGCAAAATTAAAAG[C/T]ACTTTTGTTTCTCAA	4703
rs370264178	snp	A/G/T	1.65817e-05	0.00287933	intron-variant	NEB	GRCh38.p7	2:151659048	AGAAAGATGACAACA[A/G/T]GGGGAACTATACTTA	4703
rs370265998	snp	C/T	3.31296e-05	0.00406985	missense, intron-variant	NEB	GRCh38.p7	2:151631256	TATCACTCAGTATTT[C/T]GGTAGCTCTCTTGCA	4703
rs370268300	snp	C/T	1.66161e-05	0.00288232	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151612195	ACTCACCTTGCTCAT[C/T]GTCAGGGCATTATTC	4703
rs370278293	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151690092	AATATGGAGTCCCCT[A/G]GATCTACTGAATTAG	4703
rs370284834	snp	A/T	3.40559e-05	0.00412635	missense	NEB	GRCh38.p7	2:151677566	TTTATTGTACTCACA[A/T]CACTGACTTGCTTCG	4703
rs370294616	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151545328	CGCCTGTAATTCCAG[C/T]ACTTTGGAAGGCTGA	4703
rs370296542	snp	C/T	3.34605e-05	0.00409012	missense	NEB	GRCh38.p7	2:151688353	GCATCTGCTGGTATA[C/T]GGCACTTGAACTTCT	4703
rs370313343	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151703964	TTTCCAGTTTTTCTG[C/T]TCTGTTTTTTCCCCA	4703
rs370321257	in-del	-/A	0	0	intron-variant	NEB	GRCh38.p7	2:151550290	AAAAAAAAAAAAAAA[-/A]CACTAATTCCTCTGT	4703
rs370362357	snp	A/G	1.82857e-05	0.00302366	intron-variant	NEB	GRCh38.p7	2:151710573	AATAAGACAAGCATA[A/G]CTCATGAATTGACAA	4703
rs370366011	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151515769	TACTCAGATTGACCA[A/G]TTGTTTGAAGCCATT	4703
rs370366880	snp	A/G	0.000183268	0.0095708	intron-variant	NEB, RIF1	GRCh38.p7	2:151490335	ATCAATGAGCTGGCC[A/G]GGTGGGACTGCCAAA	4703
rs370369451	snp	C/T	1.66067e-05	0.00288151	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151485792	AGTTGGCTGGGAGCA[C/T]TCCGGTCCTGCCAGT	4703
rs370372224	snp	A/C	0.0189856	0.0955633	intron-variant	NEB	GRCh38.p7	2:151550096	ACATAGCAAGATCCC[A/C]CCTCTATAAAAAATT	4703
rs370375238	snp	A/G	2.16668e-05	0.00329134	intron-variant	NEB, RIF1	GRCh38.p7	2:151516439	GATCATTGTTGTGTG[A/G]TGTGGTTTTTTTGAC	4703
rs370385896	snp	C/T	0.000236602	0.0108741	intron-variant	NEB	GRCh38.p7	2:151639811	TTTCTTTTTTGTTGA[C/T]TCAGCTTTAGGAGCC	4703
rs370416426	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151726363	AACCTGTCTTAGATT[A/G]TTTAAGGCTCTGAAC	4703
rs370421594	in-del	-/CTTT			intron-variant	NEB, RIF1	GRCh38.p7	2:151503276	TTAAGATGTTACTTT[-/CTTT]AAAAAAGATGGGTTA	4703
rs370443685	snp	C/T	1.97861e-05	0.00314526	intron-variant	NEB	GRCh38.p7	2:151688423	AGGATATTTGAACGG[C/T]TCAGGGGAACTTCTT	4703
rs370466757	in-del	-/C			intron-variant	NEB, RIF1	GRCh38.p7	2:151531308	TCTCTTTTTTTCTTT[-/C]TTTTTTTTTTTTTTT	4703
rs370467068	snp	C/T	0.000583016	0.0170636	intron-variant	NEB, RIF1	GRCh38.p7	2:151512852	TCTGTAAAACAACAC[C/T]GAATAGTTGGGTAAA	4703
rs370471076	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151612755	CAGTTGGCTCCTATG[A/T]TGTTAGGCAGTGGCC	4703
rs370477835	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151578351	AGGAAGATGGTCCTG[C/T]CCTTCTTTGATTCAT	4703
rs370502634	snp	A/G	4.97517e-05	0.00498732	intron-variant	NEB	GRCh38.p7	2:151610648	GGATAATAGACGACA[A/G]AAAATAAGAGTGTTT	4703
rs370518330	snp	G/T	3.47536e-05	0.0041684	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151516496	TCTTTGGCAGTGATG[G/T]ACGTTGGTGTTTCAA	4703
rs370534835	snp	G/T	1.65957e-05	0.00288055	intron-variant	NEB	GRCh38.p7	2:151680720	ACATATAGATAGCAT[G/T]AACACTTACATCACT	4703
rs370543734	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151511635	AAGCACAAATTCTAA[C/T]CTGGCACCACTCAAA	4703
rs370553299	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151637925	TTCCATCTAAATTCT[C/T]TAAATTATGCTCTGT	4703
rs370560106	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151616584	CTGCAATCCCAGTTA[C/T]TCGGGAGGCTGAGGC	4703
rs370560340	snp	A/T	1.66302e-05	0.00288355	missense	NEB	GRCh38.p7	2:151678080	ATACTCCCGATCTGA[A/T]TGTATCTTGGCCACG	4703
rs370566572	snp	C/T	3.53301e-05	0.00420283	missense	NEB	GRCh38.p7	2:151656179	TGCGATTCATATTCC[C/T]GGTCAGCTCAATGTT	4703
rs370572955	snp	A/G	8.28315e-05	0.00643497	missense, intron-variant	NEB	GRCh38.p7	2:151627813	GGCCGAGCTGCTTGC[A/G]GTAACCATCTTTGTA	4703
rs370595465	snp	A/G	3.32088e-05	0.00407471	missense	NEB	GRCh38.p7	2:151679989	GCAGGTTGTATTTGT[A/G]AATAATTTCCTCTCC	4703
rs370598026	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151612995	TTTTCTTTCTTTCAT[C/T]TTCTTCTTTGAATAT	4703
rs370599158	snp	G/T	0.000163987	0.00905353	intron-variant	NEB, RIF1	GRCh38.p7	2:151506159	AGTGCATTCACTGTG[G/T]CTTTACCGAGCTAAT	4703
rs370615288	snp	A/G	8.28e-05	0.00643375	missense, intron-variant	NEB	GRCh38.p7	2:151643996	GTCTTCCACTTCTCA[A/G]AGTCCTTCTTGTACT	4703
rs370623512	snp	C/T	0.000161987	0.00899818	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151619472	CTGGAGGTCATAGGC[C/T]TTCCGTGCATGAATG	4703
rs370629876	in-del	-/CT	0.00119737	0.0244387	utr-variant-3-prime, intron-variant	NEB, RIF1	GRCh38.p7	2:151485544	TATAATGGAGAAAGA[-/CT]CTAGGCACAGAAATA	4703
rs370663399	snp	C/T	1.68374e-05	0.00290145	missense	NEB	GRCh38.p7	2:151695591	ACATCACTCAAGTTA[C/T]AGGCATTGACTTTGT	4703
rs370664349	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151620304	CAGTATACTTGAAAA[C/T]GGTTAAGATGGTAAA	4703
rs370673536	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151527416	GTGGTTATTATAAAT[A/G]ATTATTCATTGTATT	4703
rs370685957	snp	A/C/T	0.000167986	0.00916322	intron-variant	NEB	GRCh38.p7	2:151625529	AATAAAACAAATGAT[A/C/T]TTACCTCACTATAAT	4703
rs370692765	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151500421	TTCAGAGTTGTATAT[A/G]ATACACAAATAATTT	4703
rs370695020	snp	A/T	6.63548e-05	0.0057596	missense	NEB	GRCh38.p7	2:151565589	TAGTTTTCAAGGGCA[A/T]TTTTCTTATATTTGA	4703
rs370696317	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151543111	GCCTGTTTCTTCTCC[A/G]AGACTAGGGCACAGC	4703
rs370738668	snp	C/T	0.000136156	0.00824982	missense, intron-variant	NEB	GRCh38.p7	2:151636274	CCACGATGGGGATGG[C/T]GTCGCTTCGCAAGTC	4703
rs370739551	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151685561	AAAAGAAGCTTCAGA[C/T]TGCAGCAGTTAAAAG	4703
rs370742146	snp	A/G	0.000116638	0.00763581	synonymous-codon	NEB	GRCh38.p7	2:151551783	CCGGTCCAGATCCAC[A/G]GTTTTGGTAGTTGGA	4703
rs370745767	snp	C/T	1.65817e-05	0.00287933	missense, intron-variant	NEB	GRCh38.p7	2:151650235	TGGCATCAGGAATGC[C/T]GGTGAACTTGTTTCT	4703
rs370748336	snp	A/C/T	4.02099e-05	0.00448367	intron-variant	NEB	GRCh38.p7	2:151625497	ATCGGCAACAATCAA[A/C/T]GTGGCCAGACCAAAG	4703
rs370750687	snp	A/T	3.42401e-05	0.0041375	missense	NEB	GRCh38.p7	2:151570081	ATGCAGCCCACTCAC[A/T]TCGCTCTGCAGTTCG	4703
rs370756059	snp	A/G			upstream-variant-2KB	NEB	GRCh38.p7	2:151734761	TTTAGTAGAAAATAA[A/G]CATGACTTTGAGAGG	4703
rs370756582	snp	A/G	0.000183655	0.0095809	missense, intron-variant	NEB	GRCh38.p7	2:151579406	GAAAGCAAGACCAGC[A/G]GTGCAGGTAATGGCG	4703
rs370764959	snp	C/T	4.98029e-05	0.00498988	missense	NEB	GRCh38.p7	2:151546377	GCCGGGAGCGGACCA[C/T]GTCAGGAGTGTCATA	4703
rs370768526	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151701033	TATTATTTTGAAATA[C/T]GTCCCATCAATACCT	4703
rs370770040	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151500710	TCAGATGAACCTCCC[A/G]CCTCAGCCTCCCAAG	4703
rs370779281	snp	A/G	8.48212e-05	0.00651179	intron-variant	NEB, RIF1	GRCh38.p7	2:151502931	ATTTAAAACAGGCAC[A/G]GAGAGTAAGGAAGGA	4703
rs370790324	snp	C/G/T	1.65693e-05	0.00287826	missense	NEB	GRCh38.p7	2:151659115	TAATCTGGGGGATAT[C/G/T]AGGCATGATGTGGAC	4703
rs370792132	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151569596	ATCCTTGATTCCATT[A/C]TGGTTATTGTTACTA	4703
rs370806634	snp	A/G	1.72308e-05	0.00293515	intron-variant	NEB	GRCh38.p7	2:151538007	CAAAGACAGCTGTAA[A/G]TCTTACCCAAAGTTA	4703
rs370810654	snp	A/G	0.000116004	0.00761504	missense	NEB	GRCh38.p7	2:151555001	ACACTTCTTGGTAAC[A/G]TATAAAGAGCTTTGA	4703
rs370819880	snp	A/G	0.000104158	0.00721581	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151490413	TCGCTGTAAGTCGAA[A/G]GGTGGTGGTCTGGTG	4703
rs370822145	in-del	-/T			intron-variant	NEB	GRCh38.p7	2:151661983	AAATAATTCCTATTC[-/T]TTTTTTTTTTAACGA	4703
rs370825760	snp	A/G	3.31378e-05	0.00407036	synonymous-codon, nc-transcript-variant, intron-variant	NEB, RIF1	GRCh38.p7	2:151506220	CTCAGGTGTCTTTCC[A/G]ATAGCCGTTCCTGGT	4703
rs370828660	snp	A/G	0.000165986	0.00910855	intron-variant	NEB, RIF1	GRCh38.p7	2:151526111	AGGCATCTGCCTGGG[A/G]CGTTCTCCCAAGAGG	4703
rs370838616	snp	A/G/T	8.47095e-05	0.00650759	intron-variant	NEB	GRCh38.p7	2:151615979	TTTGAATAAGAAATG[A/G/T]CTTTTCCAAAACATC	4703
rs370854178	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151670966	AGAAGGACGGAGGAG[C/T]GGCTCAGACACGTGT	4703
rs370860682	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151699109	TGAGTGAGAATATGC[A/G]GTGTTTGGTTTTTTG	4703
rs370873040	snp	A/G	0.000859414	0.0207116	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151514821	AGTGGGCACTACCTC[A/G]CTTGCTATTTTAGTT	4703
rs370889078	snp	A/G	0.000337943	0.0129945	intron-variant	NEB	GRCh38.p7	2:151540468	GAAATAAATGCAGAA[A/G]AGAGAGACAAGCTTA	4703
rs370895611	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151579000	GCAGGAACATCGCTT[A/G]AACCTGGGAGGCGGA	4703
rs370924370	snp	C/T	3.36848e-05	0.00410381	missense	NEB	GRCh38.p7	2:151692335	TACTCTTTGCCTTTG[C/T]CTTCTCATAGTTTTC	4703
rs370931831	snp	A/G			upstream-variant-2KB	NEB	GRCh38.p7	2:151735454	GTCCTTACACACAGC[A/G]ACAGAAATCACAGGC	4703
rs370944400	in-del	-/GT			intron-variant	NEB, RIF1	GRCh38.p7	2:151487067	TGTGTGCGCATGTGC[-/GT]GTGTGTGTACTGACA	4703
rs370953833	snp	C/G	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151676546	CTAAAAATTAGCATA[C/G]GAGTCCCTTACTAAT	4703
rs370965998	snp	A/G	0.000399208	0.0141225	NEB	2	allele_origin=G(germline)/A(germline)	2:151663587	TTTGGCCAATTCAAA[A/G]CTCATGGCATCAGGA	4703
rs370970283	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151576516	TATATATATATATAT[A/T]TTTTTTTTTTTTTTT	4703
rs370976402	snp	A/T	6.63229e-05	0.00575822	missense	NEB	GRCh38.p7	2:151678018	ACGACATTGAACATA[A/T]CATGGGGCGTGTTGT	4703
rs370986655	snp	C/T	4.96899e-05	0.00498422	missense	NEB	GRCh38.p7	2:151692112	GATATGGGTCCTCCA[C/T]GCTGCCTACATAATG	4703
rs370994489	snp	C/T	1.75111e-05	0.00295893	missense, intron-variant	NEB	GRCh38.p7	2:151625605	TAATATGGACTTGGG[C/T]CTTGTCTTTGTCCCA	4703
rs370994522	snp	C/T	7.1328e-05	0.00597151	missense	NEB	GRCh38.p7	2:151656162	CCTTACATCACTCTG[C/T]ATGCGATTCATATTC	4703
rs370996408	snp	A/G	3.33996e-05	0.0040864	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151639905	CACTTGTTCCAGAGA[A/G]TCAGTCACACTGGTA	4703
rs370999716	snp	A/G	0.000260342	0.0114063	intron-variant	NEB	GRCh38.p7	2:151666086	CTTGGTAACCAGTAC[A/G]TACATCACTCTGAAT	4703
rs371004065	snp	C/T	0.000368155	0.0135625	missense, intron-variant	NEB	GRCh38.p7	2:151592093	GAGTGTCAGCTGGCA[C/T]GTTCACATTAGCCTT	4703
rs371007266	snp	A/G	0.000167986	0.00916323	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151642667	GGCTTCTTCTAGGCC[A/G]AGCTTATACAATTTC	4703
rs371008487	snp	C/T	1.82457e-05	0.00302035	intron-variant	NEB	GRCh38.p7	2:151609781	TACATCTTCCCCTTC[C/T]CCCTTTCCCAAAATT	4703
rs371008675	snp	A/G	0.000101665	0.00712896	intron-variant	NEB	GRCh38.p7	2:151565645	GACAGGTCTACCACC[A/G]CAGGTTATCTACCCC	4703
rs371015050	snp	A/C/T	0.000353104	0.0132826	NEB	2	allele_origin=A(germline)/C(germline)	2:151724872	CTTACTGACTTGCTG[A/C/T]GACACTTTCTTTGCA	4703
rs371019748	snp	A/C	1.67136e-05	0.00289076	missense	NEB	GRCh38.p7	2:151553873	GTGATCATTGACTTG[A/C]AAGTCGGGGTGGCAA	4703
rs371027084	snp	A/G	9.56709e-05	0.00691566	missense	NEB	GRCh38.p7	2:151684975	CTTTTCGATATTCGC[A/G]CTGTGAATAGGAAAT	4703
rs371035828	snp	A/C	2.57463e-05	0.00358783	missense	NEB	GRCh38.p7	2:151733126	TAAATCTTACCTCCA[A/C]CACCTCCTCATAGTC	4703
rs371041798	snp	C/T	6.63823e-05	0.00576079	missense	NEB	GRCh38.p7	2:151663625	TGTAGGTATGGATCA[C/T]GTTCCTGTAGTTGGC	4703
rs371069626	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151522834	CCTTTGAGGTATTCC[A/G]CCTAGAGTACGCAGC	4703
rs371095047	snp	C/T	3.31395e-05	0.00407046	missense, intron-variant	NEB	GRCh38.p7	2:151627169	TGGGGACCCAGCCAA[C/T]GCCTCTCAGCCACTG	4703
rs371099860	snp	C/T	1.65734e-05	0.00287862	synonymous-codon	NEB	GRCh38.p7	2:151697452	GTAGGAATCTTTATA[C/T]TTTTTCTGCAAGACA	4703
rs371102558	snp	C/T	0.000163987	0.00905353	missense, intron-variant	NEB	GRCh38.p7	2:151610844	GAGGTTTTGTCAGCA[C/T]CCCAAGCTTCTGTGT	4703
rs371105660	snp	G/T	9.78976e-05	0.00699566	missense	NEB	GRCh38.p7	2:151684956	GTTTTTGACTTTTCA[G/T]AATCTTTTCGATATT	4703
rs371107941	snp	C/G	1.65806e-05	0.00287924	intron-variant	NEB	GRCh38.p7	2:151729683	GCACAAAGGCATTGG[C/G]AAGAGAACCAAAGCA	4703
rs371109129	snp	A/G	1.65748e-05	0.00287874	missense	NEB	GRCh38.p7	2:151656280	GCATCCTTTGCAGCC[A/G]TGACACTGAGCATGT	4703
rs371110613	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151631492	AACTAAAAGAATTAT[A/G]CTCAAAAATGACCCA	4703
rs371125812	snp	A/G	0.0003121	0.0124881	intron-variant	NEB	GRCh38.p7	2:151547385	TGAAAGCAAGCCTGC[A/G]TCTTGGTAAGACTAC	4703
rs371137550	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151711571	TAATATGTAAATAAA[C/T]AGCCAACTGGTTTTC	4703
rs371151246	snp	A/G/T	0.000229196	0.0107027	missense, synonymous-codon	NEB	GRCh38.p7	2:151662138	TGAAAGACTTACTTC[A/G/T]TTCATAATTTTTGCA	4703
rs371168880	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151601491	GGAAAAAAACAGTAT[A/T]TTTCTAGCACACATT	4703
rs371174518	snp	A/G/T	0.00062905	0.0177239	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151633753	ATAGTCCACGTCACT[A/G/T]ACTAAGGTCTGGCAC	4703
rs371175607	snp	A/G	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151685848	ATATGTGTTAGAGAC[A/G]GTGACCCAAGCTGGC	4703
rs371175998	snp	A/G	0.00015359	0.00876193	synonymous-codon	NEB	GRCh38.p7	2:151675287	AAAGACCCTACTTAC[A/G]TCACTTATATTGTAA	4703
rs371178078	snp	C/T	1.65814e-05	0.00287931	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151519729	GATTGTATTTTGGTG[C/T]CTTGCCCTTTTCTTT	4703
rs371183779	snp	A/G	0.000199734	0.00999134	intron-variant	NEB	GRCh38.p7	2:151568280	TAAGGCCCTCCACTC[A/G]TACACAAACACCAGG	4703
rs371194689	snp	A/G	7.67666e-05	0.00619495	synonymous-codon	NEB	GRCh38.p7	2:151552672	CCAGTGATCACTTAC[A/G]TCACTTAGCTGTTTC	4703
rs371201619	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151714872	TAGTACCAAAGGTAA[A/G]TCACTCTTGGCAGCC	4703
rs371201870	snp	C/T	9.94299e-05	0.00705018	synonymous-codon	NEB	GRCh38.p7	2:151538191	AATGTCTAGGGCATC[C/T]TTCACCGTGTGGTAT	4703
rs371204200	in-del	-/CATAA			intron-variant	NEB, RIF1	GRCh38.p7	2:151532357	AAATATTGTTTTACT[-/CATAA]CATATTGTATTGAAC	4703
rs371206417	snp	A/G	5.14443e-05	0.00507144	intron-variant	NEB	GRCh38.p7	2:151568023	AACTGGAATCCCTGG[A/G]AGCAAGGTCCCACTT	4703
rs371253929	snp	A/G	2.58702e-05	0.00359645	synonymous-codon	NEB	GRCh38.p7	2:151568669	ATAATCAACTCTGTC[A/G]TCCACAGGCGTAAAG	4703
rs371265681	snp	C/G	0.00033157	0.0128715	intron-variant	NEB	GRCh38.p7	2:151697464	ATATTTTTTCTGCAA[C/G]ACAAAACATACTTCA	4703
rs371270146	snp	A/G	0.00010744	0.00732861	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151493832	AGGAGTAAAGGGTGT[A/G]GGGGTTGCTTTCCCC	4703
rs371271473	snp	A/C			intron-variant	NEB, RIF1	GRCh38.p7	2:151520040	TTTCTAATGCAAAAC[A/C]AAAAAAAAAAAAAAT	4703
rs371287755	snp	A/G	6.62504e-05	0.00575507	missense	NEB	GRCh38.p7	2:151680819	TGTCTGGATGTTGGC[A/G]ATATTTTTTCTGTTT	4703
rs371300756	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151684169	AATATACTTAACACC[A/T]CTGAACTGTACACTT	4703
rs371301797	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151601644	ATTAAATCTCTTTAA[A/G]TACTTGTAAATTAAG	4703
rs371317825	snp	C/T	3.33289e-05	0.00408207	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151526167	GGTTACCTCAGACAC[C/T]AGGTTGCTGACAGTC	4703
rs371325785	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151666832	TTCCCAAAGTGCTAG[A/G]ATTAGACGTGTGAGC	4703
rs371358588	snp	A/C			intron-variant	NEB, RIF1	GRCh38.p7	2:151523971	ATCTATCCCAGGTGA[A/C]TCAAGTATGAATCAG	4703
rs371358687	in-del	-/C			intron-variant	NEB, RIF1	GRCh38.p7	2:151531304	CAACTCTCTTTTTTT[-/C]TTTCTTTTTTTTTTT	4703
rs371391123	snp	C/T	0.000165986	0.00910855	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151506273	CCTGGGCATTCAGAA[C/T]CAGGACAGTGTTAAC	4703
rs371405720	in-del	-/TGTG			intron-variant	NEB	GRCh38.p7	2:151620340	TTATATATATATGTA[-/TGTG]TGTGTATATATATAT	4703
rs371428101	snp	A/G	0.00914312	0.0669923	intron-variant	NEB, RIF1	GRCh38.p7	2:151520596	ATAGCCAGGTGTGGT[A/G]GCTCATGCCTGTAAT	4703
rs371431256	snp	A/G	0.000115937	0.00761283	NEB, RIF1	2	allele_origin=G(germline)/A(germline)	2:151524362	TATGTCTGGGCGACC[A/G]AGCATGCTTAAGCCA	4703
rs371454282	snp	C/T	0.000629306	0.0177273	missense	NEB	GRCh38.p7	2:151672608	TATAGTGGACCAGCT[C/T]GGGATCATCCTGGAG	4703
rs371465237	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151688878	GTGTGAGATTTCATC[A/G]TGCTACTCAGAACAA	4703
rs371473963	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151549530	CATCATTCTATCAGG[C/T]TGAACCTTGAGGGTG	4703
rs371490023	snp	C/T	9.93756e-05	0.00704826	missense, intron-variant	NEB	GRCh38.p7	2:151627800	GCTCCAATGTGGTGG[C/T]CGAGCTGCTTGCGGT	4703
rs371499917	snp	A/G	1.65839e-05	0.00287953	synonymous-codon	NEB	GRCh38.p7	2:151569370	GTCAGCCTTGTAAAC[A/G]TTCTGTGAAAACAGG	4703
rs371503160	snp	G/T	1.69372e-05	0.00291004	intron-variant	NEB, RIF1	GRCh38.p7	2:151485973	AAATATTATATGTTG[G/T]ATTTGCAACAGTTAA	4703
rs371515180	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151524890	CCAGGCTGGTCTCGA[A/G]CTCCTGACCTCGTGA	4703
rs371523761	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151546998	GGAGAAAAGAACAGA[C/T]TGAATGGATTGGTCT	4703
rs371542110	snp	C/T	3.31702e-05	0.00407235	missense	NEB	GRCh38.p7	2:151671154	CTGCTTTCTTGACCT[C/T]CTCCACCTCCAGGGA	4703
rs371545317	snp	A/G	9.93772e-05	0.00704831	synonymous-codon	NEB	GRCh38.p7	2:151671104	CTTGACGGTATCTGG[A/G]TGCTGTCGATACTTC	4703
rs371548550	snp	A/G	0.000165986	0.00910855	missense	NEB	GRCh38.p7	2:151696681	CTTGTAGCAGAACAG[A/G]AGAGTCTGTAACTTG	4703
rs371549127	snp	A/G	1.66029e-05	0.00288117	intron-variant	NEB	GRCh38.p7	2:151644451	CAAATCAATATCAAC[A/G]GAGGATAAAATCTTA	4703
rs371553211	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151714536	CATTCTGAAGGCTCC[C/T]GTGTGTGCATGTTAA	4703
rs371554127	snp	A/G	3.31559e-05	0.00407147	synonymous-codon	NEB	GRCh38.p7	2:151662300	CAGAGGGAGCCATCC[A/G]ATGCCCTTCATGAAG	4703
rs371554739	snp	G/T	1.65583e-05	0.00287731	missense, intron-variant	NEB	GRCh38.p7	2:151627621	TGTAGTCCACATCGC[G/T]GACTAAGGTCTGGCA	4703
rs371565168	snp	A/G	4.96866e-05	0.00498406	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151644097	ACCAATGTGGTGGCC[A/G]AGCTGCTTGCGAAAG	4703
rs371568550	snp	C/T	0.000281758	0.0118659	missense, intron-variant	NEB	GRCh38.p7	2:151619521	AGGCAGATCCATTCA[C/T]GCAGAGGATGTTTAT	4703
rs371570995	snp	A/G	4.9703e-05	0.00498488	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151644489	GGCAATTTCCCGGGA[A/G]GCTTTTGCTGCTTTG	4703
rs371572709	snp	C/T	0.000323948	0.0127228	missense, intron-variant	NEB	GRCh38.p7	2:151619617	CTGCTGTACCTTGTC[C/T]TGTATTTCTCAAAAT	4703
rs371591500	snp	C/G			missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151485916	AGCCATATAGTCATA[C/G]ATGGCACGGAAGATT	4703
rs371598031	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151607143	TACCTAGCCCGCCAT[C/T]TGGATGTAAATAGAA	4703
rs371598760	snp	C/T	1.7205e-05	0.00293295	missense	NEB	GRCh38.p7	2:151727888	TTGTTGTCGTAGTCT[C/T]ATAAATTTTTGTTAT	4703
rs371600800	snp	A/G	0.000110888	0.00744525	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151490507	GCTCCCGGCTCCGGC[A/G]CTGAGCTTGGACTGG	4703
rs371605774	snp	C/T	0.00949149	0.0682324	missense, intron-variant	NEB	GRCh38.p7	2:151621016	TCTTCCATGGCCTGA[C/T]GATAGAGGCTCTGAG	4703
rs371611266	snp	A/G	1.80598e-05	0.00300493	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151526215	AGGCGTGTCAGGTAC[A/G]GCATGGCAGGTTCCT	4703
rs371615634	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151649990	GACAAAAACTGACAC[G/T]GACCCATTTTTACAT	4703
rs371634536	snp	A/G	0.000169986	0.00921759	intron-variant	NEB	GRCh38.p7	2:151733192	ACCTACAAACTTTTC[A/G]TATTCCATACAAATG	4703
rs371639543	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151733852	ATAGGATTGTCAGTC[C/T]TTAGCCTAAGCTTCT	4703
rs371639863	snp	C/T	5.00221e-05	0.00500085	missense	NEB	GRCh38.p7	2:151665389	CCATTGTGTCCATGG[C/T]GTAAGTGAACTTCAG	4703
rs371658494	snp	A/G	3.31846e-05	0.00407323	synonymous-codon	NEB	GRCh38.p7	2:151697574	CTGCAGAACAGTATC[A/G]AGCTTGAATTTGGGG	4703
rs371669095	snp	C/G/T	9.51415e-05	0.00689659	synonymous-codon	NEB	GRCh38.p7	2:151563913	CTTGGTGCCCTCCCA[C/G/T]GCCCCTTTATACAGT	4703
rs371670376	snp	C/T	3.32027e-05	0.00407434	synonymous-codon	NEB	GRCh38.p7	2:151663662	GGCCACTTCCTGAGA[C/T]TTCTTGGCTGCCACC	4703
rs371675358	snp	A/G	0.000116135	0.00761933	missense, intron-variant	NEB	GRCh38.p7	2:151612229	GCTAGGACAATTTCC[A/G]GAGTGTCGGTAATGC	4703
rs371675749	snp	C/G	0.00011635	0.00762635	intron-variant	NEB	GRCh38.p7	2:151618250	GGTAACTTTCGGTAT[C/G]TAACAGTGAGGATTG	4703
rs371680259	snp	A/T	1.65803e-05	0.00287922	missense	NEB	GRCh38.p7	2:151538231	GTCTTTTGAAATGTT[A/T]CTTTGTAGCGTAGCT	4703
rs371681892	snp	C/T	1.71053e-05	0.00292444	missense	NEB	GRCh38.p7	2:151570313	GCTATGAGGGCCCAG[C/T]GGATCTTGTTGTCAT	4703
rs371689870	snp	A/G	4.08097e-05	0.00451699	missense	NEB	GRCh38.p7	2:151562672	TCTTCCAGAAGAGAC[A/G]TCCACTGGTGGAAAT	4703
rs371691551	in-del	-/GTATGTATGTAT			intron-variant	NEB	GRCh38.p7	2:151660368	CTTGTGTGTATGTAT[-/GTATGTATGTAT]ATCTTTGCACACATA	4703
rs371704528	snp	C/G	4.87781e-05	0.00493829	missense	NEB	GRCh38.p7	2:151535735	AATGCCTATTGATCG[C/G]AGAGTCGGCAACATA	4703
rs371710158	snp	C/G	1.6566e-05	0.00287797	missense	NEB	GRCh38.p7	2:151679767	GCTCTGATGGGAATC[C/G]CATCAGTTCTCAGGT	4703
rs371711395	in-del	-/T			intron-variant	NEB	GRCh38.p7	2:151564334	AATTTTTGTATTTTT[-/T]AGTAGAGATGGGGTT	4703
rs371713922	snp	C/T	8.3176e-05	0.00644834	intron-variant	NEB, RIF1	GRCh38.p7	2:151505429	GCACCAGGGTAGCAA[C/T]TGAGAGATGGCCAGT	4703
rs371720016	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151622813	ATATTCAAATTTCAT[C/G]AAATGTCCCAATAAT	4703
rs371724109	snp	A/C	0.00318978	0.0398085	intron-variant	NEB, RIF1	GRCh38.p7	2:151486182	TTCCCCCACCAAAAG[A/C]GGCAAAGGATATGAA	4703
rs371738434	snp	A/G	0.000559304	0.0167134	intron-variant	NEB	GRCh38.p7	2:151657966	CCCAGCCAGGTGACC[A/G]TTTCCTTTGGACTTA	4703
rs371740288	snp	C/T	0.000163987	0.00905353	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151630754	CCTTGCCAACATAAT[C/T]TCTGGTGTATCAGGC	4703
rs371740292	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151522265	CTGAAGAACAGTCCC[A/G]AGAATTAGAAAAGCT	4703
rs371771414	snp	C/G	4.99214e-05	0.00499582	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151609881	GCATGTCCATTCATG[C/G]AGGTAATTGCGATAA	4703
rs371778394	snp	A/G	6.07995e-05	0.00551326	intron-variant	NEB	GRCh38.p7	2:151690837	TATGCTAGAAAAGAA[A/G]ATGTTCTTTAATGAA	4703
rs371780078	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151542803	TCAAATCTATTCTTC[A/G]TAGAAATAATTCTTC	4703
rs371783915	snp	C/T	6.61981e-05	0.0057528	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151490503	GACTGCTCCCGGCTC[C/T]GGCGCTGAGCTTGGA	4703
rs371785128	snp	A/G	9.95454e-05	0.00705427	synonymous-codon	NEB	GRCh38.p7	2:151553897	GTGGCAAATCCATTC[A/G]TGGAGGCGCAGGCGG	4703
rs371786629	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151567111	TCTGGGATGTTGCTC[A/G]TCATTCTCAGAGTGT	4703
rs371791129	snp	A/G	0.000231706	0.010761	intron-variant	NEB	GRCh38.p7	2:151717526	TGTAGGCAACCTGAT[A/G]AAATAAAAGACAGGG	4703
rs371812340	snp	A/G	6.63768e-05	0.00576056	intron-variant	NEB	GRCh38.p7	2:151655799	GGGAGCTGTGTGGAC[A/G]GCCACTGTTCTCTGT	4703
rs371816204	snp	C/T	1.67492e-05	0.00289384	missense	NEB	GRCh38.p7	2:151677896	TCTGTATCTGCATCA[C/T]GTTCTTAGACAGCTC	4703
rs371819541	snp	C/G/T	1.65957e-05	0.00288055	missense, synonymous-codon	NEB	GRCh38.p7	2:151655988	ACTCCAGCCAAGCCC[C/G/T]TTGTACCATTCATTG	4703
rs371822291	snp	A/C	2.08797e-05	0.00323101	missense	NEB	GRCh38.p7	2:151665496	TCTATGGGCACCCAG[A/C]CGATCCCTTTCATCC	4703
rs371835861	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151503903	AATGTTCCTCGCTGG[C/T]TCCTAATCTGTAGGA	4703
rs371857325	in-del	-/AAG			intron-variant, utr-variant-3-prime	NEB, RIF1	GRCh38.p7	2:151497576	TTTAAATCATGAAAG[-/AAG]TTTTCAAAATCATTA	4703
rs371868090	snp	A/G	0.000654296	0.0180754	intron-variant	NEB	GRCh38.p7	2:151567134	CAGAGTGTACCATGC[A/G]TTTCTAGATAATGAA	4703
rs371895415	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151638502	AGATTTGTTCTGTGC[A/T]GCTTCAGAGGACTAT	4703
rs371901612	in-del	-/AAATT			intron-variant	NEB	GRCh38.p7	2:151677437	ACTGTAATTTTTAAA[-/AAATT]AAATAAACAAAATAA	4703
rs371903766	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151710152	AAAAAGAGTCCCTTT[A/G]ACTTGTACTAATCTC	4703
rs371907218	snp	A/T	4.97591e-05	0.00498769	intron-variant	NEB	GRCh38.p7	2:151729588	TTAATGAGAATGCAG[A/T]TTATGCAGCTGTGGG	4703
rs371909976	snp	A/C/T	0.000174068	0.00932787	missense	NEB	GRCh38.p7	2:151682709	TTTCCATTTCTAAGG[A/C/T]CCCAAAAGGCACCCA	4703
rs371915921	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151593568	TAACATCAGTTGGAT[C/T]TTAGGAGGTAAAGAA	4703
rs371928978	snp	C/T	0.000592303	0.0171989	intron-variant	NEB	GRCh38.p7	2:151640704	AGTCATCTGTTTTAA[C/T]TTTTAGTAAAAAGCA	4703
rs371937219	snp	A/G	1.8e-05	0.00299995	intron-variant	NEB	GRCh38.p7	2:151612395	TGTAAATAGCCTGAA[A/G]ATGAAATAATGTCAA	4703
rs371938654	snp	A/G	4.97913e-05	0.00498931	missense	NEB	GRCh38.p7	2:151662224	TGTCTGGGTGCTGGC[A/G]GTACTTCTTTTCACT	4703
rs371956053	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151701507	TCCTGGACTCTTTTT[A/G]GTTGGTAAACTATTG	4703
rs371959881	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151683297	GGCTAACAAAACACT[G/T]TAAAACAGTTGCACT	4703
rs371962475	snp	C/T	0.000246722	0.0111041	synonymous-codon	NEB	GRCh38.p7	2:151665450	ACTAAGAATCTCTCC[C/T]GCTTTCTTTGCCTTC	4703
rs371963286	in-del	-/AGGA			intron-variant	NEB	GRCh38.p7	2:151578693	GGAAGGAAGGAAGGA[-/AGGA]GAGAAGGAGGGAAGG	4703
rs371982926	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151709585	TTTTACTAATTATAT[A/G]CAAGAGCCAAAGTTA	4703
rs371991383	snp	A/T	1.6669e-05	0.00288691	missense, nc-transcript-variant, intron-variant	NEB, RIF1	GRCh38.p7	2:151506914	GTAAATATACCGAGC[A/T]GAAATTCTTCTGATT	4703
rs371998749	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151633404	AAATGTCTCCCTCTA[C/G]TGGACCCTGAATTCT	4703
rs372005148	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151513522	ACAGAGGGACACTTT[A/G]TGTCCTTAAAGTTAC	4703
rs372024982	snp	G/T	0.000167986	0.00916323	synonymous-codon	NEB	GRCh38.p7	2:151568367	CAGCAGGGGGGTTTC[G/T]GTGAGGGTGTACTTT	4703
rs372037674	snp	C/G	2.03048e-05	0.00318622	missense	NEB	GRCh38.p7	2:151560674	CTGGTGGCTTTCACT[C/G]TATCCCAGGCCTCCT	4703
rs372041287	snp	C/T	1.73021e-05	0.00294121	missense	NEB	GRCh38.p7	2:151655329	GTGTATCAGGCATCA[C/T]ATGAATCTTGGTCTT	4703
rs372042301	snp	C/T	0.000313463	0.0125153	missense	NEB	GRCh38.p7	2:151547506	TCATGTGGCCCTGCA[C/T]CTTGAAGAAGTCTGA	4703
rs372049328	snp	C/T	0.000215401	0.0103757	missense	NEB	GRCh38.p7	2:151576242	ACCACAGGCGTCCGA[C/T]AGACACTGTCACAAA	4703
rs372053480	snp	C/T	1.65641e-05	0.00287781	missense, intron-variant	NEB	GRCh38.p7	2:151627554	TAGGCCTGCCGAGCA[C/T]GGATGACATCATTCT	4703
rs372061947	snp	A/G	3.34594e-05	0.00409006	intron-variant	NEB, RIF1	GRCh38.p7	2:151529169	GTCCTACAGAAGCTG[A/G]TAAATCCCCCACCAT	4703
rs372073855	in-del	-/AAAA			intron-variant	NEB	GRCh38.p7	2:151550287	AAAAAAAAAAAAAAA[-/AAAA]CACTAATTCCTCTGT	4703
rs372092324	snp	A/T	2.71102e-05	0.00368162	intron-variant	NEB, RIF1	GRCh38.p7	2:151516589	AAAGCCATGTTAGAT[A/T]TCTCTCCTCTGGTCA	4703
rs372106749	snp	A/G	3.31246e-05	0.00406955	missense	NEB	GRCh38.p7	2:151694355	CCACCTTCAAGGAGT[A/G]CAGCATCTTGGGATC	4703
rs372111642	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151540829	AGAAAGTGAGGTGTC[A/G]TAGAGATAAAGCATT	4703
rs372113031	snp	A/G	0.000149538	0.0086456	intron-variant	NEB, RIF1	GRCh38.p7	2:151485940	GAAGATTTTCTATTC[A/G]TGGGGATGGAAAAGG	4703
rs372116910	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151584195	TAACATATATTCCAG[A/T]TGGGGAAAACAAGGC	4703
rs372117694	snp	A/G	0.000746485	0.0193051	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151503372	AGTTCTCTTGATTGC[A/G]TTTGACTCTCTCAAT	4703
rs372122164	snp	C/G	0.0314385	0.121371	intron-variant	NEB	GRCh38.p7	2:151581905	TAAAAGGTGCCAATA[C/G]TGACTTCAATAAGAA	4703
rs372123788	snp	C/T	0.000167986	0.00916322	intron-variant	NEB, RIF1	GRCh38.p7	2:151519812	TTCCTGGACATCAAT[C/T]AATTTGGGAATTGGG	4703
rs372132667	snp	A/C	3.31241e-05	0.00406952	missense, intron-variant	NEB	GRCh38.p7	2:151650776	TTGTATTCTCTTTCA[A/C]TCTGCATTTTGGCTA	4703
rs372138506	snp	A/G			synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151640619	ACGTATAGCTCGGGC[A/G]CCAATGTGGTGGCCG	4703
rs372143763	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151505718	GTGTGAATGGGACCT[C/T]ATTCTGATACTGGGT	4703
rs372183545	snp	C/T	2.19952e-05	0.00331619	intron-variant	NEB	GRCh38.p7	2:151565668	TCTACCCCAACATGG[C/T]AGGTAGGAGGACAGG	4703
rs372199850	snp	C/T	1.65921e-05	0.00288024	synonymous-codon	NEB	GRCh38.p7	2:151541519	TGAAGTAAAGATTGA[C/T]TTCTGCTTCTTGCCT	4703
rs372203426	snp	A/G	8.34941e-05	0.00646065	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151492440	TCTCGGGGGTATCCA[A/G]TACATAGGCAGCTTT	4703
rs372217127	snp	A/G	0.000314655	0.0125391	missense	NEB	GRCh38.p7	2:151687483	TCATTAATGCTGAGG[A/G]CTCCAATCATTTTCC	4703
rs372224380	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151669386	AAGGCATATCTGTCC[C/T]GTTGGAGCTTACTGT	4703
rs372228043	snp	A/G	6.67713e-05	0.00577764	missense, intron-variant, utr-variant-3-prime	NEB, RIF1	GRCh38.p7	2:151497633	CAAAGTACCGAGCTA[A/G]TATTTTCTTGATTGT	4703
rs372236577	snp	C/T	1.65858e-05	0.00287969	synonymous-codon	NEB	GRCh38.p7	2:151697187	AATTGCTTCATATTC[C/T]TGAGTTATGGTCTGA	4703
rs372239158	snp	A/G	1.65649e-05	0.00287788	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151629557	ACTGATAACGTCCCT[A/G]GAGGCCTTGGCAGCC	4703
rs372241831	snp	C/T	0.000215583	0.01038	intron-variant	NEB	GRCh38.p7	2:151554045	AAAGTTAAAATCACA[C/T]GCCAGTTATACAGGA	4703
rs372245772	snp	A/G	0.000167986	0.00916323	missense, intron-variant	NEB	GRCh38.p7	2:151616024	GCAATATCTCTTGAA[A/G]CCTTGGCTGCTTGGA	4703
rs372247757	snp	A/T	0.000159987	0.00894247	missense	NEB	GRCh38.p7	2:151570177	GCGGTAATCCATGTC[A/T]CTGACCAGAGCCTGG	4703
rs372248515	snp	A/G	1.65614e-05	0.00287757	missense, intron-variant	NEB	GRCh38.p7	2:151643206	GTATGGAATCCATAA[A/G]GCTGGAAAACTTAAA	4703
rs372252328	snp	A/C/T	0.000250199	0.0111822	intron-variant	NEB	GRCh38.p7	2:151545848	TTCAGTTTGTACTGG[A/C/T]CAATTTGATTGACTT	4703
rs372259638	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151492792	AATTACAGCATCAAC[A/G]TATTCGATGGTATTT	4703
rs372267179	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151730610	ACACTTGGCTCATTT[C/T]TTAGTGAAAAAAAAA	4703
rs372271428	snp	A/G	0.000161987	0.00899818	missense	NEB	GRCh38.p7	2:151562663	ACATTGGGTTCTTCC[A/G]GAAGAGACGTCCACT	4703
rs372279388	snp	A/G	0.00023393	0.0108125	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151519022	CAGAGACTCCTTCAT[A/G]TCAGTCACGGGTTTG	4703
rs372283650	snp	A/C	1.65745e-05	0.00287871	missense, intron-variant	NEB	GRCh38.p7	2:151609931	TCTGACATTTCTTGG[A/C]CAGCAAGATGCTTAA	4703
rs372284984	snp	C/T	0.000447631	0.0149538	missense, intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151534291	TGGTATTTATCTTTC[C/T]GCTGCTCATAATCAG	4703
rs372285797	in-del	-/G			intron-variant	NEB	GRCh38.p7	2:151671988	GAGTTAATAAAGGAA[-/G]AAAAAAAAACACCTT	4703
rs372326115	snp	A/G	9.21022e-05	0.00678547	intron-variant, synonymous-codon	NEB, RIF1	GRCh38.p7	2:151533538	CTTGGCACTAGATTT[A/G]TATTTTCTCTGTCCA	4703
rs372328578	snp	C/T	0.0209421	0.100162	intron-variant	NEB, RIF1	GRCh38.p7	2:151517996	CCTGACTCCCTATAA[C/T]CTACTGTAGTGTTCC	4703
rs372350585	snp	C/G/T	6.7944e-05	0.00582816	intron-variant	NEB	GRCh38.p7	2:151636367	AAAATCAGATGCTGA[C/G/T]ATTTATATCTAAAAA	4703
rs372356574	snp	C/G	0.00137576	0.0261914	intron-variant	NEB	GRCh38.p7	2:151614254	TTCTAAACCATTACT[C/G]AAGAATATTAGAGCC	4703
rs372371053	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151716023	AAACATTTAAAAATA[G/T]ATTCCTTTTTCTTTC	4703
rs372378614	snp	A/G	1.72439e-05	0.00293627	intron-variant	NEB, RIF1	GRCh38.p7	2:151492380	TCCTAAAGAATTCCT[A/G]ACTCACCGTTGAGAT	4703
rs372378973	snp	A/G	1.66208e-05	0.00288273	missense	NEB	GRCh38.p7	2:151576197	AGGACCACTTCAGGT[A/G]TGTCAACAATGCTTG	4703
rs372386615	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151625299	TTGAGATATTTTTTC[C/T]CTCCTGAAATGAAGA	4703
rs372387518	snp	A/G/T	0.000195084	0.00987441	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151513623	GCCCTCATAAAATCC[A/G/T]GAGTTTCATTGGCCA	4703
rs372391157	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151683774	CATGCCCATATTCAT[A/G]GCAGCATTATTCAAA	4703
rs372391684	snp	C/G	1.74579e-05	0.00295443	missense	NEB	GRCh38.p7	2:151551842	AGTCATAGTGGTAGA[C/G]AGCCTGGTGCAGAAA	4703
rs372409953	snp	C/T	0.000184111	0.00959279	missense, intron-variant	NEB	GRCh38.p7	2:151592128	TTCTCCCAGGCATTG[C/T]GATACAATGGCTGGG	4703
rs372447162	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151731345	CTCTCTCTTTCTTTT[C/T]AAGTTTAAGTTAGAG	4703
rs372454928	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151661127	AACTCTGCAATGGGA[C/G]GATTCAACTTGATGG	4703
rs372470491	snp	A/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151495747	CATTTTTAAGTAAGT[A/T]AATTGATAATCAATA	4703
rs372473041	snp	C/T	4.53206e-05	0.00476007	intron-variant	NEB	GRCh38.p7	2:151547574	CATATGTATTAGAGA[C/T]CGAATGATTAACATT	4703
rs372475028	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151706456	ACACAATTAGAAAGT[C/G]CTGTGAAGACTTAGG	4703
rs372487130	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151619787	AGAATCCAGTAAATA[A/G]GAAGGAAGCACAAAG	4703
rs372525290	snp	C/T	3.37786e-05	0.00410952	intron-variant	NEB, RIF1	GRCh38.p7	2:151526286	GCAGGAAAAGGGGCA[C/T]TTCTTTAGCTCTGCT	4703
rs372540293	snp	C/T	0.000273124	0.0116828	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151496309	ATTGTGTTTGACTCG[C/T]TCCATCTCGGGAGTG	4703
rs372545569	snp	A/G	0.00755907	0.0610114	intron-variant	NEB	GRCh38.p7	2:151719798	GTGAGAGGATCACTT[A/G]AGCCTGGGAGGTGGA	4703
rs372552087	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151701789	TGCTAGCAGTCTATC[A/T]ATTTTGTTGATCCTT	4703
rs372553629	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151632841	TAAGCAATCTGTCAA[A/T]ATTGTCGTTGTATGG	4703
rs372554238	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151701598	TTTAGTCTTGGGAGA[G/T]TGTATGTGTCGAGGA	4703
rs372554545	in-del	-/TGAGATAG			intron-variant	NEB, RIF1	GRCh38.p7	2:151519139	TAATGGAAATCAAAG[-/TGAGATAG]CCCATCGTCAAACAA	4703
rs372554892	snp	G/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151522712	AAGACAGAAATAATG[G/T]CTTGCTGGTCTCAGT	4703
rs372579696	snp	C/G/T	6.63013e-05	0.00575733	missense	NEB	GRCh38.p7	2:151725548	TTTTCTCAAACTTCT[C/G/T]CTTGTATTTATTCTG	4703
rs372580033	snp	A/T	5.54985e-05	0.00526746	intron-variant	NEB	GRCh38.p7	2:151724221	ATATATGATGGGATG[A/T]CATAGGAAGACAGAA	4703
rs372593815	snp	A/C/T	0.000248721	0.0111492	synonymous-codon	NEB	GRCh38.p7	2:151678026	GAACATATCATGGGG[A/C/T]GTGTTGTATTTGGAC	4703
rs372607126	snp	C/T	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151619895	GCTGCTGTAACGCCA[C/T]ATATTGGACTGTTGT	4703
rs372609682	snp	C/G/T	0.000248428	0.0111426	synonymous-codon	NEB	GRCh38.p7	2:151692116	TGGGTCCTCCATGCT[C/G/T]CCTACATAATGTCCC	4703
rs372630401	in-del	-/GTCTT			intron-variant	NEB	GRCh38.p7	2:151688220	ACAATTCCTTGTCTT[-/GTCTT]TTAAAATTTAAAACA	4703
rs372633207	snp	A/C/G/T	0.000232417	0.0107776	intron-variant	NEB	GRCh38.p7	2:151694299	CCACGTCTGAAAATA[A/C/G/T]GGGTGAATTACAAAG	4703
rs372640666	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151520084	GGCTAAATTCAGAGA[C/T]GTGATTTAATGTACT	4703
rs372645309	snp	C/T	0.000159987	0.00894249	intron-variant	NEB	GRCh38.p7	2:151724848	CAGCCATCCATATCA[C/T]TGCCTTACCTTACTG	4703
rs372649635	snp	A/G	0.000169986	0.00921759	intron-variant	NEB	GRCh38.p7	2:151666439	CAGAAGTTGGCTAGC[A/G]TAGAAGTCTGATATA	4703
rs372653139	snp	A/C			missense	NEB	GRCh38.p7	2:151537210	ACCAATGCCTTTAAG[A/C]CAAGTCAAGTCTTCT	4703
rs372655602	snp	C/G	1.68043e-05	0.0028986	missense, intron-variant	NEB	GRCh38.p7	2:151650869	AGTTGCTTTCGGTAG[C/G]CTTGTTTGTATTTAT	4703
rs372661728	in-del	-/T			intron-variant	NEB	GRCh38.p7	2:151637299	TCAGTAGACTAAGGT[-/T]GGCATCAAGTGCAGA	4703
rs372664114	snp	C/T	1.66194e-05	0.00288261	synonymous-codon	NEB	GRCh38.p7	2:151679730	ACTTACGTCACTCGC[C/T]GCCTGCCTGGCAGCT	4703
rs372667149	snp	C/T	0.000165761	0.00910235	missense	NEB	GRCh38.p7	2:151656404	ATTTGGGATCATCCT[C/T]GAGACTGCGGAAACC	4703
rs372668101	snp	A/G	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151670197	AATTAACCCTTAGAC[A/G]TCTGTGATAATGTGG	4703
rs372669969	snp	C/T	3.31246e-05	0.00406955	missense, intron-variant	NEB	GRCh38.p7	2:151640033	AGCCAATGCCTCTCA[C/T]CCACTGGAGATCAGA	4703
rs372676278	snp	C/T	1.6574e-05	0.00287867	missense	NEB	GRCh38.p7	2:151697216	GAGGGAAGAAGCCTT[C/T]GCCTCTGTCTTCTTC	4703
rs372680461	snp	C/T	1.658e-05	0.00287919	missense	NEB	GRCh38.p7	2:151674493	TCACTGGCAATGTTT[C/T]TCGATGCCTTGGCTG	4703
rs372680599	snp	A/C/G	3.3166e-05	0.00407211	intron-variant	NEB, RIF1	GRCh38.p7	2:151514281	CAAAGAAATGATGCT[A/C/G]TATGAATTACGTGCA	4703
rs372689662	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151505721	TGAATGGGACCTCAT[C/T]CTGATACTGGGTAAG	4703
rs372694084	snp	A/G	3.48147e-05	0.00417207	missense	NEB	GRCh38.p7	2:151672397	TGATTGACATTCCTC[A/G]TATGCTCAAGACTCA	4703
rs372699411	snp	C/T	8.27986e-05	0.0064337	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151514394	GTGAGGCCCTTCCCA[C/T]GGATGCTTTCCTCTA	4703
rs372703032	snp	A/G	1.6638e-05	0.00288422	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151490077	TTTGCATGTTTGTAA[A/G]CTGAAAAAAAGGGGG	4703
rs372724145	snp	A/G			synonymous-codon	NEB	GRCh38.p7	2:151684817	CTTGGCAAGGTCCAC[A/G]TTGATGCTATCAGGG	4703
rs372726513	snp	C/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151715778	GCTGACTTATATACT[C/G]AGTTTATACTGATCA	4703
rs372731855	snp	A/C	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151641413	CATGTCTCACTGCAA[A/C]CTCCAACTCTTGGGC	4703
rs372739191	in-del	-/AGTA	0.00279162	0.0372561	intron-variant	NEB, RIF1	GRCh38.p7	2:151503003	TAGTAAGTAATATTT[-/AGTA]AGGATAATGTTTTTA	4703
rs372740184	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151704554	CAGGTGCAGGATATA[A/G]TCTCGTGGTGCGCCG	4703
rs372754098	snp	A/G	5.0683e-05	0.00503378	synonymous-codon	NEB	GRCh38.p7	2:151570237	GTCCACAGGGCTCTG[A/G]ATCTTGGCCTTCCAT	4703
rs372755514	snp	A/C/G	3.33763e-05	0.004085	intron-variant	NEB, RIF1	GRCh38.p7	2:151518462	CACATTGATGGAGAA[A/C/G]CTGCTCAGCATTCCT	4703
rs372762302	snp	A/G	8.28878e-05	0.00643716	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151492100	CAGGCTCAGTTACCT[A/G]TAATAGTCTCCTGAT	4703
rs372763273	snp	C/T	0.000165986	0.00910854	missense	NEB	GRCh38.p7	2:151691890	GGTCCAGCTTCTTGA[C/T]TGCTTCATATTCTTG	4703
rs372772045	snp	C/T	1.65957e-05	0.00288055	missense	NEB	GRCh38.p7	2:151548396	GCCTTGGTGTGTTCA[C/T]AGGCTTCTTTGTACT	4703
rs372772607	snp	A/G	1.66147e-05	0.0028822	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151614288	CACATCACTCTGCAG[A/G]TCATAGGCCTTCCGA	4703
rs372778072	snp	C/T	0.084364	0.187256	intron-variant	NEB	GRCh38.p7	2:151601341	CTCGAACTCCTGACC[C/T]CAAGTGATCCACCCG	4703
rs372780802	snp	A/T	2.60468e-05	0.0036087	missense	NEB	GRCh38.p7	2:151665523	ATCCAATTGGTGAAG[A/T]CAGATTTGTACAGAT	4703
rs372786852	snp	C/T	6.63493e-05	0.00575936	synonymous-codon	NEB	GRCh38.p7	2:151569283	CTCACTGAAGATGTC[C/T]GCGGCATGTTTGGCA	4703
rs372787876	snp	C/G	3.7145e-05	0.00430942	intron-variant	NEB	GRCh38.p7	2:151625512	TGTGGCCAGACCAAA[C/G]AAATAAAACAAATGA	4703
rs372788442	snp	C/T	1.67245e-05	0.00289171	missense	NEB	GRCh38.p7	2:151665406	TAAGTGAACTTCAGC[C/T]TCTCGGGGTGCTGGC	4703
rs372797159	snp	C/T	1.855e-05	0.00304543	intron-variant	NEB	GRCh38.p7	2:151547605	CATCCCTAGTCTCTA[C/T]TCCCTGTCTTTCCTA	4703
rs372800812	snp	G/T	0.000175663	0.0093702	missense	NEB	GRCh38.p7	2:151655373	TCAATGGTGTATAAA[G/T]GCTAGGAAGTGGGAA	4703
rs372803182	snp	A/G	1.65581e-05	0.00287728	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151627616	GTTCTTGTAGTCCAC[A/G]TCGCTGACTAAGGTC	4703
rs372804275	snp	C/T	3.67033e-05	0.00428373	intron-variant	NEB	GRCh38.p7	2:151642558	CTAAGGCAAATAACT[C/T]TCCAAGTATACTTAC	4703
rs372804439	snp	C/T	0.000369368	0.0135848	missense	NEB	GRCh38.p7	2:151562693	TGGTGGAAATAGTGT[C/T]GATACTCCAGGTCAC	4703
rs372808358	snp	C/T	0.000739836	0.019219	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151527002	ACCCTTGAGGAACTC[C/T]CGGTCCAGCTTATAT	4703
rs372813378	in-del	-/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151489757	TGCTCTAGGTTTGGG[-/T]TTTTTTTTTTAAGTT	4703
rs372819467	snp	C/T	3.04048e-05	0.00389891	intron-variant	NEB	GRCh38.p7	2:151568611	TTTAAAACAGCCATA[C/T]ACTTACATCATCGAG	4703
rs372827767	snp	C/T			missense, intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151534286	CCAGGTGGTATTTAT[C/T]TTTCCGCTGCTCATA	4703
rs372856725	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151520822	TGAGTCAGGATCGCA[C/T]CACTGCACTCCATCG	4703
rs372863074	snp	C/T	5.5622e-05	0.00527332	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151493809	TTGCGTTTCACTCTT[C/T]CCATCTCAGGAGTAA	4703
rs372877088	snp	A/G	0.000659585	0.0181482	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151531045	CAACATGGGTGTGTC[A/G]TGGATTGTGGTGTAG	4703
rs372905711	snp	G/T	4.99397e-05	0.00499673	intron-variant	NEB	GRCh38.p7	2:151610509	GAGTTAGATGGAAGG[G/T]ACTCACGTCACTGGC	4703
rs372906589	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151728875	GCTAATAGGTTGTTT[C/T]CTGCCCATGATTACC	4703
rs372910723	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151699160	GAATGATGATTTCCA[A/G]TTTCATCCATGTCCC	4703
rs372936552	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151564755	TTCTATCAATTTAAG[C/T]CTGTTCCCCTCACTT	4703
rs372984467	in-del	-/T	0.0337553	0.125452	intron-variant	NEB, RIF1	GRCh38.p7	2:151491422	CAATAGAATTACTAC[-/T]GTTTTTTCTTTGGAA	4703
rs372991820	in-del	-/CTA			intron-variant	NEB	GRCh38.p7	2:151560045	AGGATGTATGATCTT[-/CTA]CTATATTTAAACAGC	4703
rs373007581	snp	A/C	0.00835141	0.0640778	intron-variant	NEB	GRCh38.p7	2:151609278	AGCACATGGGGTTGA[A/C]GGGATAAGTGCACGA	4703
rs373014903	snp	A/G	0.000163987	0.00905352	intron-variant	NEB	GRCh38.p7	2:151549773	AGCAGGTTAAATGAC[A/G]TCGGGCATCAAGTAA	4703
rs373019444	in-del	-/A	0.0182019	0.0936463	intron-variant	NEB	GRCh38.p7	2:151564131	GACTCGAGGCATTTT[-/A]TTTTTTATTTTATTT	4703
rs373043006	in-del	-/ACAA			intron-variant	NEB, RIF1	GRCh38.p7	2:151509365	AAAGAATAGAAACAA[-/ACAA]TCGTCCTTTTATTTT	4703
rs373043905	snp	C/T	0.000165986	0.00910855	intron-variant	NEB	GRCh38.p7	2:151695552	GTTGTCAGTACATCA[C/T]ATGGTACAGGGCATA	4703
rs373058243	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151658286	CAAACTTAAACATAT[A/T]TTCAAGAAAATACCA	4703
rs373064894	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151638369	AGAGTCACATTTTAC[C/T]AGTGATGTCATGTGA	4703
rs373069408	snp	C/T	0.000134463	0.00819837	intron-variant	NEB	GRCh38.p7	2:151669148	TAAAAACAAAGGAGA[C/T]AGCATGCACATATCA	4703
rs373105485	snp	C/T	0.000155988	0.00883005	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151514347	GAGTGGCATTCTTTG[C/T]TCTTAGCATGTCAGG	4703
rs373107685	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151641202	CTAAAATAATTTGTT[A/G]TGATTCGTGTGTGAG	4703
rs373115276	in-del	-/ATG			intron-variant	NEB, RIF1	GRCh38.p7	2:151496723	ACTCATTTTTAAAAA[-/ATG]ATGATTGAAAATATC	4703
rs373118761	snp	A/G	3.31631e-05	0.00407191	synonymous-codon	NEB	GRCh38.p7	2:151678005	TTTCTTAGCCGCCAC[A/G]ACATTGAACATATCA	4703
rs373133009	snp	A/G/T	0.000295563	0.0121532	missense, synonymous-codon	NEB	GRCh38.p7	2:151723457	GTAAAACAAACTTTT[A/G/T]TCTGCTTCCCAGTCT	4703
rs373134363	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151674727	TTGGCAAAGTGTCAC[A/G]CTGTGTGTAGCATGA	4703
rs373141155	snp	C/G	3.31625e-05	0.00407188	intron-variant	NEB	GRCh38.p7	2:151729606	ATGCAGCTGTGGGCT[C/G]GGCCTTACCTCTCCC	4703
rs373141570	snp	A/C	0.167484	0.23599	intron-variant	NEB	GRCh38.p7	2:151601572	AAATTATTATAGGAA[A/C]CACCGGTAGTATACA	4703
rs373162293	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151607156	ATCTGGATGTAAATA[A/G]AAATGGTCTTTTGTC	4703
rs373164962	snp	G/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151493637	CTCGTGGGGTTGGTT[G/T]GTTGTTTTTAAGTGG	4703
rs373166434	snp	C/T	8.90972e-05	0.00667388	intron-variant	NEB	GRCh38.p7	2:151663521	ATTATCCAGAGTAAA[C/T]GCTCTGCAAATGTGG	4703
rs373168257	snp	C/G	3.56856e-05	0.00422392	missense	NEB	GRCh38.p7	2:151684858	AACTGTGTAAGATGT[C/G]CTTATAATCAACGTC	4703
rs373188212	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151567748	AAAAAATATATACTT[A/G]TTCTCTGATTCTGGC	4703
rs373191528	snp	A/G	2.76951e-05	0.00372112	intron-variant	NEB, RIF1	GRCh38.p7	2:151530960	TAGAAGGAGGCCAAG[A/G]TGAGAGGGACTGCTA	4703
rs373197639	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151698901	TACTTTAAGTTTTAG[C/G]GTACATGTGCACATT	4703
rs373197663	snp	C/T	0.000265481	0.0115182	intron-variant	NEB, RIF1	GRCh38.p7	2:151505617	TTATTACATGCTGGA[C/T]TGTTATTCTTCCCAA	4703
rs373225058	snp	A/C/G/T	9.94563e-05	0.00705129	intron-variant	NEB	GRCh38.p7	2:151679857	GTCATTTAAGTACAA[A/C/G/T]TTAGAGACTGTGTTA	4703
rs373232042	snp	C/G	6.67668e-05	0.00577745	intron-variant	NEB	GRCh38.p7	2:151709620	AAATTTACCCACACT[C/G]AAACCATCAAGATAA	4703
rs373234291	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151723288	ACATTTAGTCTCTTA[C/T]ACAGAAGAGTTGCAG	4703
rs373238925	snp	C/G/T	3.38669e-05	0.00411491	intron-variant	NEB	GRCh38.p7	2:151694494	TGTCCCCGAAGCCAG[C/G/T]CTGTCCAGGTCCCCA	4703
rs373246130	snp	A/C	3.41023e-05	0.00412917	missense, intron-variant	NEB	GRCh38.p7	2:151654080	TTCAAAGCTTCTTCC[A/C]ATCCAAGTTTATAGA	4703
rs373250411	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151702584	ATTTAGGATAGTTAG[C/T]TCTTCTTGTGGAATT	4703
rs373252601	snp	G/T	0.000167986	0.00916322	missense, intron-variant	NEB	GRCh38.p7	2:151643331	ATGCCTTTTAGCCAC[G/T]GAAGGTCTGACTTGT	4703
rs373258662	snp	A/G	0.000232161	0.0107716	synonymous-codon	NEB	GRCh38.p7	2:151677975	ATAGTTGACATTGCT[A/G]ACCACATCCTGGGCT	4703
rs373259828	snp	A/G	0.000140974	0.00839447	intron-variant	NEB	GRCh38.p7	2:151568064	CACTCCCATCAGGAT[A/G]TATTACCTCACTCTG	4703
rs373263895	snp	A/G	8.36603e-05	0.00646708	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151519031	CTTCATGTCAGTCAC[A/G]GGTTTGTGAAGTTTC	4703
rs373264501	snp	C/T	0.000106773	0.00730581	intron-variant	NEB	GRCh38.p7	2:151717562	TTTTAAAAACGATTA[C/T]GCTTTCATCTTTATT	4703
rs373269210	snp	A/C	0.000165986	0.00910854	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151512745	TACCTGGCTTGAAAG[A/C]TTCTTGACTTGTTGG	4703
rs373276853	snp	G/T	2.14245e-05	0.00327289	missense	NEB	GRCh38.p7	2:151570528	CTGGAGGCCTTGGCA[G/T]CCTGGATGGGGATGG	4703
rs373276952	snp	A/G	0.000161987	0.00899818	synonymous-codon	NEB	GRCh38.p7	2:151546381	GGAGCGGACCATGTC[A/G]GGAGTGTCATACAGG	4703
rs373278622	snp	A/C/T	0.000132598	0.00814144	synonymous-codon	NEB	GRCh38.p7	2:151655895	AAACTGGAAGTTGCT[A/C/T]GGGTGCTGGCGGTAT	4703
rs373285394	snp	A/T	1.65605e-05	0.0028775	missense, intron-variant	NEB	GRCh38.p7	2:151627707	CACTTCTCAAAGTCC[A/T]TCTTATACTCCCTGT	4703
rs373299798	in-del	-/A	0.00438332	0.0466095	intron-variant	NEB, RIF1	GRCh38.p7	2:151520396	CTTCAGAATAATGAG[-/A]AAAAATAAGATTAAA	4703
rs373328073	snp	A/G	9.38659e-05	0.00685012	synonymous-codon	NEB	GRCh38.p7	2:151669045	ACTCATGTTGAGGGC[A/G]TTGACTTTGGCTTGA	4703
rs373353657	snp	A/G	0.000149067	0.00863199	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151643860	AGCATGGATGACATC[A/G]CTCTGGTCGGGCAGG	4703
rs373359731	in-del	-/AT	0.00676609	0.0577691	downstream-variant-500B, intron-variant	NEB, RIF1	GRCh38.p7	2:151485311	TTAAAACCATTAAAC[-/AT]AAATAATGCTCATTC	4703
rs373360468	snp	C/T	0.000260383	0.0114072	intron-variant	NEB, RIF1	GRCh38.p7	2:151493902	GCCCGAAAGTCACTA[C/T]GAGGTAATAATCACT	4703
rs373365702	snp	A/G	0.000347921	0.0131848	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151618365	TTCTGGACGCTGACG[A/G]TAGATAGTATCACTA	4703
rs373371474	snp	A/T	6.96403e-05	0.00590045	intron-variant	NEB	GRCh38.p7	2:151562815	GTAGTTCAACTAATA[A/T]GTTTTAAAGACAAAA	4703
rs373385805	snp	C/T	1.65655e-05	0.00287793	missense, intron-variant	NEB	GRCh38.p7	2:151627090	TTGTCCGGAGGCTGG[C/T]GGTAGATGTTATCAC	4703
rs373390654	snp	A/C/T	0.000760583	0.0194862	intron-variant	NEB	GRCh38.p7	2:151567484	TTGTATTTCAGCTGG[A/C/T]GAGAAGAGGAATATA	4703
rs373412519	snp	C/T	0.000169985	0.00921758	intron-variant	NEB	GRCh38.p7	2:151646267	AATTTTTCAGTGGTG[C/T]TGTTAGATTAGTGAA	4703
rs373421444	snp	A/G	0.0205511	0.0992634	intron-variant	NEB	GRCh38.p7	2:151625340	TCTGTCTGTCTATCT[A/G]TCTGTCTAATCTATC	4703
rs373426420	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151733021	CTCTTTGTGAAGTTA[C/T]AATAGACAATGTATT	4703
rs373439650	snp	A/C/G	0.000281987	0.0118707	missense	NEB	GRCh38.p7	2:151655965	TCCACTTCCAGAGAA[A/C/G]CTGCTGGACTCCAGC	4703
rs373449008	snp	A/G	0.00011647	0.00763029	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151642619	TGCCTTGATAGGAAT[A/G]GCATCTACCCGCATG	4703
rs373453206	snp	A/G	0.000331186	0.012864	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151633942	GTGGCCAAGTTGCTT[A/G]CAGTAACCATCTTTA	4703
rs373461387	snp	C/T	3.33056e-05	0.00408065	intron-variant	NEB	GRCh38.p7	2:151562077	GATTCTGATGACCCA[C/T]GGAGAACCAGTCCTT	4703
rs373468992	in-del	-/C			intron-variant	NEB, RIF1	GRCh38.p7	2:151520039	CTTTCTAATGCAAAA[-/C]AAAAAAAAAAAAAAA	4703
rs373471062	snp	A/G	1.65638e-05	0.00287778	missense, intron-variant	NEB	GRCh38.p7	2:151614490	TCACTCTGGATCTTG[A/G]CCACATGGATGGACC	4703
rs373475161	snp	C/T	2.69676e-05	0.00367193	intron-variant	NEB, RIF1	GRCh38.p7	2:151531128	AAAAGCAGAAAGACA[C/T]CATGTCATGCTTCTC	4703
rs373491741	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151557498	ACAGAAAAAGAGAGA[A/C]TCCTCCCTAACTCAT	4703
rs373503374	snp	A/G	6.76842e-05	0.005817	intron-variant	NEB	GRCh38.p7	2:151535833	ACTTGACAGCAGGCT[A/G]TGATTATCTTAAGAA	4703
rs373548410	in-del	-/T			intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151507254	TTGCTTAGTAGATTT[-/T]AACTTTGAAAAAGAT	4703
rs373551215	snp	A/G	0.000353115	0.0132828	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151490504	ACTGCTCCCGGCTCC[A/G]GCGCTGAGCTTGGAC	4703
rs373563301	snp	A/C	1.81046e-05	0.00300865	synonymous-codon	NEB	GRCh38.p7	2:151684898	TGCCTGAGATTTCTT[A/C]GCTTGAGTGACTTGG	4703
rs373581480	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151689274	CAGTGACACAATCTC[C/G]GCTCACTGCAACCTC	4703
rs373587647	snp	C/T	0.00127992	0.025265	missense, intron-variant	NEB	GRCh38.p7	2:151636282	GGGATGGCGTCGCTT[C/T]GCAAGTCATAGCCTT	4703
rs373588820	snp	G/T			missense, intron-variant	NEB	GRCh38.p7	2:151646232	AGCTTCTCTATAAAG[G/T]CTCTAAAATAAGAAA	4703
rs373589529	snp	C/T	0.000132611	0.00814173	missense, intron-variant	NEB	GRCh38.p7	2:151650264	CTGTCTGGAGGCTGA[C/T]GATATTTCTTCTCAC	4703
rs373594030	in-del	-/CTT			intron-variant	NEB, RIF1	GRCh38.p7	2:151496069	GAAAATCTGTTACTT[-/CTT]GATATTAGAACTTTA	4703
rs373618445	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151631672	GACAGAAACCACACC[C/T]GTGCCCAACATCAGG	4703
rs373632181	snp	G/T	0.00597247	0.0543191	intron-variant	NEB	GRCh38.p7	2:151668306	GCTTATAGGAAGATA[G/T]GAATACTAAAACTAA	4703
rs373634428	snp	A/C/T	0.000767235	0.0195714	intron-variant	NEB	GRCh38.p7	2:151692007	AGATCATGATTGTTA[A/C/T]GGCTCTCAAACAATG	4703
rs373635403	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151672022	ATAGAAGAATTTTCT[A/G]TCCTTCCTGAATTTG	4703
rs373635811	snp	A/G	0.0111196	0.0737302	intron-variant	NEB	GRCh38.p7	2:151609504	AAATTTTGCTGAATT[A/G]GATTCCATTTTAATC	4703
rs373652428	snp	A/G	6.66733e-05	0.00577341	synonymous-codon	NEB	GRCh38.p7	2:151727841	TGCCAGAGCTGGTTT[A/G]GAAGTTTCTGATTGC	4703
rs373699055	snp	A/T	1.67916e-05	0.0028975	missense	NEB	GRCh38.p7	2:151677574	ACTCACATCACTGAC[A/T]TGCTTCGTGTTCTGT	4703
rs373705550	snp	C/T	0.000105219	0.00725247	missense	NEB	GRCh38.p7	2:151687673	CCAACAGGGGAATGG[C/T]GTCCACTTTAATGTC	4703
rs373713314	snp	C/T	1.72071e-05	0.00293313	missense	NEB	GRCh38.p7	2:151655310	TTGGCTTGTAAAATA[C/T]CTGGTGTATCAGGCA	4703
rs373721189	snp	A/G	5.60491e-05	0.00529353	missense	NEB	GRCh38.p7	2:151664826	GGCATGACATGAATG[A/G]TGGTCTTGTCCTTGT	4703
rs373729655	snp	C/T	1.68032e-05	0.0028985	missense	NEB	GRCh38.p7	2:151724961	CCATTCGATACTTAA[C/T]CTGCCCAAATAATGC	4703
rs373742185	snp	C/G	0.00392137	0.0441057	intron-variant, missense, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151498243	GTGGCATTTTTTCCC[C/G]TTTCTTTCCAAAATA	4703
rs373748568	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151632367	CTAGTTATTGCCCCA[C/T]AAATAACAATAGCAA	4703
rs373748794	snp	A/C	9.9486e-05	0.00705217	synonymous-codon	NEB	GRCh38.p7	2:151672636	GAGGCTTCTGAAACC[A/C]ACATGCTTTCCCTTT	4703
rs373750915	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151732870	ATTAAAACCTGCCTT[C/T]ACTCCAACTTGGTTT	4703
rs373751073	snp	A/C	1.65954e-05	0.00288053	intron-variant	NEB	GRCh38.p7	2:151610668	TAAGAGTGTTTGAGG[A/C]AGGTAATAGGCCAAT	4703
rs373755540	snp	C/G	1.65971e-05	0.00288067	missense	NEB	GRCh38.p7	2:151697548	GGATTGCTTACATCA[C/G]TACTGAAGTTCTGCA	4703
rs373758264	in-del	-/GTAA			intron-variant	NEB, RIF1	GRCh38.p7	2:151495745	TTCATTTTTAAGTAA[-/GTAA]ATTGATAATCAATAA	4703
rs373778424	snp	C/T	0.000106916	0.0073107	missense	NEB	GRCh38.p7	2:151656166	ACATCACTCTGTATG[C/T]GATTCATATTCCTGG	4703
rs373790988	snp	A/G	0.000760384	0.0194837	missense	NEB	GRCh38.p7	2:151664532	CTAGAGGCTCTTGCA[A/G]CCTTTATTGCAATGG	4703
rs373793316	snp	C/T	4.96915e-05	0.0049843	missense, intron-variant	NEB	GRCh38.p7	2:151631273	GTAGCTCTCTTGCAC[C/T]TGACCACATCCATAG	4703
rs373796976	snp	C/T	0.000167986	0.00916322	synonymous-codon	NEB	GRCh38.p7	2:151709752	GTTTTCAAAATCTTC[C/T]TGGTATTTCCTCTGT	4703
rs373799650	snp	A/G	0.000161987	0.00899818	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151640358	CTCAGTACTCACATC[A/G]CTCTGGAGGTCATAG	4703
rs373804545	snp	A/G	1.66454e-05	0.00288486	intron-variant	NEB	GRCh38.p7	2:151569413	TCAGCAACCCTGGTC[A/G]TGTGGTCCTAGTTAG	4703
rs373818296	snp	A/C	0.000288845	0.0120141	intron-variant	NEB	GRCh38.p7	2:151650561	TAAACTATTGGATTT[A/C]ATAGAAACTGACCTC	4703
rs373823362	snp	A/G	0.000105417	0.00725929	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151625609	ATGGACTTGGGTCTT[A/G]TCTTTGTCCCAGGCT	4703
rs373827041	snp	G/T	1.66621e-05	0.00288631	missense, intron-variant	NEB	GRCh38.p7	2:151639909	TGTTCCAGAGAGTCA[G/T]TCACACTGGTAAATT	4703
rs373829936	snp	C/G	0.000158165	0.00889144	missense, intron-variant	NEB	GRCh38.p7	2:151609841	AGGCCTTTTTTGCTT[C/G]GATAATGTCGTTTTG	4703
rs373833313	snp	C/T	3.31235e-05	0.00406948	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151631221	AAATTTCAGCTTGTC[C/T]GGAGGCTGGCGGTAG	4703
rs373834327	snp	C/T			intron-variant, utr-variant-3-prime	NEB, RIF1	GRCh38.p7	2:151497365	AACTCAGTGGTGTTA[C/T]CCACACAAACTGAAA	4703
rs373844031	snp	A/G	2.54075e-05	0.00356414	intron-variant	NEB	GRCh38.p7	2:151565648	AGGTCTACCACCACA[A/G]GTTATCTACCCCAAC	4703
rs373850451	snp	A/C/T	0.000139733	0.00835745	NEB	2	allele_origin=A(germline)/C(germline)	2:151570591	TCATCCCAGCCCTCA[A/C/T]GGTAAAGTTTCTGAA	4703
rs373850463	in-del	-/TCTA	0.00119737	0.0244387	intron-variant	NEB, RIF1	GRCh38.p7	2:151507622	TCACACTTCCGCATC[-/TCTA]TCCATAAAAATACAC	4703
rs373852098	snp	A/G	5.82326e-05	0.00539564	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151514850	TTGCATATTTGACAT[A/G]TAACAAAGCTGGCGT	4703
rs373854612	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151514107	ATAGATTATGATAAC[C/T]ACTACAGAAACACAC	4703
rs373858974	snp	C/T	1.66194e-05	0.00288261	synonymous-codon	NEB	GRCh38.p7	2:151692297	AGTATCAAGTTGATA[C/T]TTTGGGGTCTCACAG	4703
rs373861490	snp	C/G	1.65603e-05	0.00287747	synonymous-codon	NEB	GRCh38.p7	2:151666225	TGCAGCTGTCACACT[C/G]ACCATATCCAGAGGT	4703
rs373866669	in-del	-/TTA			intron-variant	NEB	GRCh38.p7	2:151634726	GCAACCGAGGAGAAT[-/TTA]TTATTATTATTATTA	4703
rs373868916	snp	A/G	0.000169986	0.00921759	missense, intron-variant	NEB	GRCh38.p7	2:151642859	TTATCCCAAGCTTCT[A/G]TATAGAGGCGCTAAG	4703
rs373871239	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151612821	GCATTACTGGTTGAT[C/T]ACGTTGCATTAATGT	4703
rs373883986	snp	A/G	3.31846e-05	0.00407323	missense	NEB	GRCh38.p7	2:151697576	GCAGAACAGTATCGA[A/G]CTTGAATTTGGGGGT	4703
rs373888482	snp	G/T	1.71123e-05	0.00292504	intron-variant	NEB	GRCh38.p7	2:151672703	GGCAGAATTGGGTTA[G/T]CAAAGTCCTAGGCAT	4703
rs373892420	snp	C/T	8.29125e-05	0.00643812	missense	NEB	GRCh38.p7	2:151687426	ACACTCACATCACTC[C/T]GGTTTTTGGCTGTCT	4703
rs373895191	snp	A/G	0.000464206	0.0152279	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151650678	CCACGTCACTAACCA[A/G]CTCCTGACACTTCTT	4703
rs373903232	snp	A/C	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151664092	CGAAGAGATGTGTAA[A/C]TAAATTGGTTTAGAG	4703
rs373922594	snp	C/T	1.67911e-05	0.00289746	intron-variant	NEB	GRCh38.p7	2:151540666	TATTTTTCTTTTTAC[C/T]CAGTGCCTCAGTGCT	4703
rs373926259	snp	C/T	0.000188968	0.00971845	intron-variant	NEB	GRCh38.p7	2:151672362	GTCTGTTGTTACACA[C/T]ACTTACATCACTCTG	4703
rs373945534	snp	A/G	0.000165986	0.00910855	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151526948	AGTATTCCTGAGGGC[A/G]AGCACCGTGTTTTTG	4703
rs373946062	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151500467	TCAGCAACAATATTA[A/G]TAAAAGATAACATTA	4703
rs373946448	snp	A/G	0.00126679	0.0251354	synonymous-codon	NEB	GRCh38.p7	2:151690754	TTTCGTGTTGAGCTG[A/G]GCTTGCAACAGTACA	4703
rs373946758	snp	C/G	0.000843455	0.0205187	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151527570	TGTTGGCTTCGTACT[C/G]TTTCTTATAGTCCAG	4703
rs373969894	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151502683	AAAACTGAGGTAATA[C/T]TTGGTATCATTATTT	4703
rs373981344	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151494471	ACCCTTGAGGACTGC[A/G]AGAGAGACCTGTGGT	4703
rs373982126	in-del	-/ATATATATATATA			intron-variant	NEB	GRCh38.p7	2:151576504	TATATATATATATAT[-/ATATATATATATA]TTTTTTTTTTTTTTT	4703
rs373984704	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151729069	AGGTATTTCACCTTG[A/G]AAAAAAAAAGAGCTT	4703
rs373993514	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151618009	AGGTTGCAGTGAGCC[A/G]AGATCGTGCCATTGC	4703
rs374002871	snp	C/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151528140	AGCTGGAATTTAAAC[C/G]CAGGCAGTCTGGCTG	4703
rs374003090	snp	A/G	0.000109312	0.00739215	intron-variant	NEB, RIF1	GRCh38.p7	2:151531913	TAAATTGTGGAAGAG[A/G]AGAAAGAGCTCTAAG	4703
rs374029795	snp	C/G	3.31274e-05	0.00406972	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151506178	TACCGAGCTAATGTG[C/G]TCCTGTGTTTGTTTC	4703
rs374039131	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151708328	ATCTTCAATTTCCCT[C/T]TTTTCATTCACTTGT	4703
rs374044989	snp	A/C/T	0.000251999	0.0112223	intron-variant	NEB	GRCh38.p7	2:151670991	ACGTGTGGTTATTTA[A/C/T]GGGCAAATCATTTTG	4703
rs374096746	in-del	-/AC			intron-variant	NEB	GRCh38.p7	2:151568602	TGTGAGATTTTAAAA[-/AC]CAGCCATATACTTAC	4703
rs374114696	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151628906	AAAAACAAAAGAAAA[A/G]AAGAAGAAGAAGAAG	4703
rs374142041	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151509313	GATGACTCCTTAGCT[A/G]TGTAGATGTAAGGAA	4703
rs374142869	snp	A/T	5.04359e-05	0.00502149	intron-variant	NEB, RIF1	GRCh38.p7	2:151519788	CAGCAAATGCAAACA[A/T]CCAAATTATTCCTGG	4703
rs374151310	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151632189	CTGAAGGTTTTTATA[C/T]ACCCATTAGATATTC	4703
rs374153115	snp	A/G			intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151534528	GGATAGGTCAGATTT[A/G]TGACACCAAAATTAG	4703
rs374155853	snp	C/T			synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151612360	CCATCCTATGCCTCT[C/T]AGCCACTCAAGATCA	4703
rs374157764	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151494937	ACAGGCGTGAGCCAC[C/T]ACACCTGGCCCACAG	4703
rs374180094	snp	A/T	8.67416e-05	0.00658508	intron-variant	NEB	GRCh38.p7	2:151664658	TTATTGGGGTTAGAA[A/T]AGAGGTCCTGACTAC	4703
rs374182560	snp	C/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151513174	CCAATGAGCATTAGA[C/G]AAGCTAAGATGCCTA	4703
rs374185098	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151529692	TGCGCCACCTCACCC[A/G]GCTAATTTTGTATTT	4703
rs374205890	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151556483	TACAGAAAATGTTCC[C/T]GATTAAGAGATAAAG	4703
rs374214388	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151690028	CTGTTCAAAGAGTAG[C/G]CTACCAATCACAGCA	4703
rs374227241	snp	A/C/G	0.000126688	0.007958	intron-variant	NEB	GRCh38.p7	2:151724370	TGTATAAAACCTAGA[A/C/G]AGAAGGAGCAGAGGA	4703
rs374230433	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151616714	TAACAAAACAAAACA[A/C]AACAGTATTTATTAT	4703
rs374266734	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151572853	CCATGCCCAGCCAAG[G/T]ATGTATATATTTTTA	4703
rs374281356	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151651056	TCCCTAGTAGCTGGG[A/G]TTTACAGGTACATGC	4703
rs374287903	snp	A/G	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151692689	AGAAAAATGAGTTTC[A/G]CTAGGTGCAGGGGCT	4703
rs374318711	snp	A/C	0.000171527	0.00925926	intron-variant	NEB	GRCh38.p7	2:151717367	CTGATGGTTGAAATT[A/C]TTAAGCAGAGTCTTC	4703
rs374323430	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151717288	GTAGAGTCTTTGGGG[A/G]TCATATGTAAAAATA	4703
rs374331837	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151646634	AGGAAGTTTTATTTC[C/T]TATGTGGCTTATTGT	4703
rs374341745	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151678860	GGGTGAGAACTTCGG[A/G]TGGGACAGGGGCATT	4703
rs374345029	snp	C/T	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151626891	TCAACTGAATCACTA[C/T]ACATTGGATAGCAAT	4703
rs374345951	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151569099	ATATTATGGATGTGG[C/T]CCCATAATGTGATAG	4703
rs374359052	snp	C/G/T	0.000215246	0.010372	missense, intron-variant	NEB	GRCh38.p7	2:151627591	GCAGGCACGTCCACT[C/G/T]GTGCAGGTAGTTCTT	4703
rs374368246	snp	A/G	1.65833e-05	0.00287948	intron-variant	NEB, RIF1	GRCh38.p7	2:151505467	ATGGAAGCTGAGAGT[A/G]TGGCCACTACCGAGC	4703
rs374373873	in-del	-/AAG			intron-variant	NEB, RIF1	GRCh38.p7	2:151505223	TGATAATTAATTAAG[-/AAG]CCAAGTCCATGAGCT	4703
rs374375884	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151698041	ATTGCACTCCAGCCC[A/G]GGCGACAATGCGAGA	4703
rs374382175	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151576518	TATATATATATATAT[A/T]TTTTTTTTTTTTTTT	4703
rs374388899	snp	C/T	0.00318978	0.0398085	intron-variant	NEB	GRCh38.p7	2:151676267	CCTTTAAGAACAATA[C/T]CTAAGCAATGACAGA	4703
rs374390581	snp	C/T	0.000101722	0.00713095	missense	NEB	GRCh38.p7	2:151733144	CCTCCTCATAGTCTT[C/T]GTCATCTGCCATTTT	4703
rs374396459	snp	A/G/T	3.74576e-05	0.00432754	intron-variant	NEB	GRCh38.p7	2:151610137	TAAAATGCCAGAAAT[A/G/T]CAGGTGGAGACATCC	4703
rs374409067	snp	A/G	0.000150793	0.0086818	intron-variant	NEB	GRCh38.p7	2:151687369	CTACCCTTGGGCATC[A/G]TAACAGGGAGTCCAT	4703
rs374410062	snp	A/G	0.000163987	0.00905353	synonymous-codon	NEB	GRCh38.p7	2:151567399	TGCATGCTCAAACCA[A/G]ACCAGCTTAGGATCA	4703
rs374412508	snp	A/G	1.65778e-05	0.002879	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151485917	GCCATATAGTCATAC[A/G]TGGCACGGAAGATTT	4703
rs374413679	snp	A/G	0.000182202	0.00954295	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151492128	GATCTTGGTCATTCC[A/G]TTTTTGTTCCATTTC	4703
rs374422239	snp	C/G	0.000341769	0.0130678	intron-variant	NEB	GRCh38.p7	2:151546312	ATCCAGCTGTGCGGG[C/G]GGTAATTATGCATTG	4703
rs374433039	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151701231	CACTTGATCATGGTG[A/G]ATAAGCTTTTTGATG	4703
rs374439684	snp	A/C	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151681612	GTTTTCATCGAAAAC[A/C]AAACACCGAACAAGA	4703
rs374440932	snp	C/G	3.31246e-05	0.00406955	synonymous-codon	NEB	GRCh38.p7	2:151671092	CACACTTGTGAACTT[C/G]ACGGTATCTGGGTGC	4703
rs374444328	snp	C/T	9.48452e-05	0.00688575	intron-variant	NEB	GRCh38.p7	2:151630833	CGCTATAAAAGAAGA[C/T]AAGATGCTGATTAAA	4703
rs374445549	snp	A/G	1.66518e-05	0.00288542	intron-variant	NEB	GRCh38.p7	2:151644433	GAAGTGATAAATTGC[A/G]ATCAAATCAATATCA	4703
rs374461410	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151701412	ATTCCCTCTTTTTCT[A/G]TTGATTGGAATAGTT	4703
rs374463547	snp	A/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151664708	ATGCAGACATAAGTA[A/T]CAGTTCCCTTTAACC	4703
rs374466769	snp	C/T	1.65622e-05	0.00287764	missense, intron-variant	NEB	GRCh38.p7	2:151640398	GCATGGATGACGTCG[C/T]TCTGGTCGGGCAGGC	4703
rs374468605	snp	A/C/T	3.31369e-05	0.00407032	missense, intron-variant	NEB	GRCh38.p7	2:151619546	GTTTATAGTCCACAT[A/C/T]GCTGACCAAGGTCTG	4703
rs374470965	snp	A/G	6.08217e-05	0.00551427	intron-variant	NEB	GRCh38.p7	2:151655224	TTATTTTATAAGTTC[A/G]TAAGTTTCAATACAA	4703
rs374471394	snp	C/G	3.32049e-05	0.00407448	missense, intron-variant	NEB	GRCh38.p7	2:151627203	ATCAGATTTGTAAAT[C/G]TTCTGGAGAGATTAA	4703
rs374475460	snp	A/T	7.74863e-05	0.00622392	intron-variant	NEB	GRCh38.p7	2:151642762	TATGAATATATTACT[A/T]ACCTCACTGTAATTT	4703
rs374476761	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151659489	TATTTTTTGTAGAGA[C/T]GGGTTTTTGCCATGT	4703
rs374477471	snp	C/T	7.92299e-05	0.00629354	intron-variant	NEB	GRCh38.p7	2:151610870	TGTGTATAAATGCTA[C/T]AGGGCAGGGCGGCAT	4703
rs374478409	snp	G/T	9.31858e-05	0.00682526	intron-variant	NEB	GRCh38.p7	2:151552648	TTTATTACTGTCCAC[G/T]TAACTTCCCCAGTGA	4703
rs374482369	snp	C/T	0.000159987	0.00894247	intron-variant	NEB	GRCh38.p7	2:151568192	TACTGAAAGACAGAG[C/T]CACCATAAAGGGTTA	4703
rs374484102	snp	A/G	0.000880958	0.0209691	intron-variant	NEB	GRCh38.p7	2:151538025	TTACCCAAAGTTAAT[A/G]TAAATATGGCTTCTT	4703
rs374486286	snp	A/C/T	0.000116108	0.00761856	missense, intron-variant	NEB	GRCh38.p7	2:151614565	TGGCCAAGCTGTTTG[A/C/T]GGTAGCCTTCCTTGT	4703
rs374486889	snp	C/T	4.9717e-05	0.00498558	intron-variant	NEB	GRCh38.p7	2:151563747	TTAAACATTGAGAAT[C/T]GCTGGAGTTTCCTAA	4703
rs374487720	snp	C/G	0.00010605	0.00728106	intron-variant	NEB	GRCh38.p7	2:151560555	GCAGGGGAGGGGAGG[C/G]AGGGTGGGAAAGCTG	4703
rs374494479	snp	C/G	2.55614e-05	0.00357492	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151490461	TTCTCCTCACCCCCA[C/G]TGATGCTTAGTGCAC	4703
rs374499643	snp	C/G	0.000232984	0.0107906	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151506261	CTTTATATAAAACCT[C/G]GGCATTCAGAATCAG	4703
rs374503714	snp	A/G	0.000182302	0.00954556	intron-variant	NEB, RIF1	GRCh38.p7	2:151526113	GCATCTGCCTGGGGC[A/G]TTCTCCCAAGAGGGA	4703
rs374505298	snp	C/G	7.07001e-05	0.00594517	utr-variant-3-prime, intron-variant	NEB, RIF1	GRCh38.p7	2:151485722	CATTGACTGCAGGAT[C/G]TGTAAGTCCTGCAGA	4703
rs374511864	snp	C/G	0.000437904	0.0147905	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151501469	CCCCTTGCTCAAGTT[C/G]TCTTTGTACAATATC	4703
rs374513817	snp	A/G	5.05421e-05	0.00502678	intron-variant	NEB, RIF1	GRCh38.p7	2:151529321	GTATTTCAGCTGTGG[A/G]AGGAAACACAGTGAC	4703
rs374516019	snp	A/G	5.83606e-05	0.00540157	intron-variant	NEB, RIF1	GRCh38.p7	2:151519101	AAGAAAGGAAATCAC[A/G]TAAATAGGAAATGGA	4703
rs374520321	snp	A/T	5.61656e-05	0.00529902	intron-variant	NEB	GRCh38.p7	2:151547410	GACTACTCCAGAAAG[A/T]CCCCTACGAGATGCT	4703
rs374528765	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151691638	CCAAATTCGTGTAGA[C/T]ATAAACTAATGAAAA	4703
rs374534499	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151529680	GGACCACAGGCATGC[A/G]CCACCTCACCCGGCT	4703
rs374538366	snp	A/C/G	0.000204817	0.010118	synonymous-codon	NEB	GRCh38.p7	2:151724287	GGCGGTGTTCTTAAC[A/C/G]GCCTGGACAAGTTCA	4703
rs374553944	snp	A/C/G	0.00105235	0.0229162	intron-variant	NEB	GRCh38.p7	2:151565618	GATCTGTAAAGAAAC[A/C/G]GAGACAATTAAGACA	4703
rs374557429	snp	A/G	0.000161987	0.00899817	missense	NEB	GRCh38.p7	2:151553835	AGGCTTACATCGCTG[A/G]TCTGATCTGTGACTT	4703
rs374558726	snp	C/T			upstream-variant-2KB	NEB	GRCh38.p7	2:151735668	TTTGGGAGGCCGAGG[C/T]GGGCAGATTGTCTGA	4703
rs374560223	snp	C/T	0.00159617	0.0282053	intron-variant	NEB, RIF1	GRCh38.p7	2:151512191	GCCTGCCACCACGCC[C/T]GGCTAATTTTTGTGT	4703
rs374562457	snp	A/C			splice-donor-variant	NEB	GRCh38.p7	2:151710433	TCCCTTCCCACTTAA[A/C]TGTGCTAATGTTATC	4703
rs374575419	snp	C/G	1.65924e-05	0.00288027	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151503380	TGATTGCGTTTGACT[C/G]TCTCAATCTCTGGAG	4703
rs374581669	snp	C/T	0.000159987	0.00894249	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151524349	TCTTGGCCATTTCTA[C/T]GTCTGGGCGACCGAG	4703
rs374586028	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151633494	TTCTTATGAAGTCTA[C/T]TAGTGTATTCATAAT	4703
rs374606967	snp	A/G	0.000159904	0.00894016	missense	NEB	GRCh38.p7	2:151562643	GGGCGTTTCGGACGC[A/G]TATAACATTGGGTTC	4703
rs374609793	snp	A/G	9.20514e-05	0.0067836	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151592094	AGTGTCAGCTGGCAC[A/G]TTCACATTAGCCTTC	4703
rs374619990	snp	A/G	6.70264e-05	0.00578867	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151534195	CCTGCCTGGGCCACC[A/G]GCCAGCCCCATCACA	4703
rs374650537	in-del	-/AA			intron-variant, utr-variant-3-prime, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151498173	AGCAAAGAAGGGAAA[-/AA]TGGGCTTCAAACAAA	4703
rs374656230	snp	A/C/T	5.64637e-05	0.00531306	missense, stop-gained, intron-variant, utr-variant-3-prime	NEB, RIF1	GRCh38.p7	2:151497661	TGTGTTTGACTCTTT[A/C/T]CATCTCGGGAGTGAC	4703
rs374662309	snp	C/G	5.00029e-05	0.0049999	synonymous-codon	NEB	GRCh38.p7	2:151546357	CACCCAGAGCTTCCG[C/G]AGGTGCCGGGAGCGG	4703
rs374677022	snp	C/G	3.12984e-05	0.00395578	missense	NEB	GRCh38.p7	2:151664533	TAGAGGCTCTTGCAG[C/G]CTTTATTGCAATGGC	4703
rs374682217	snp	A/C	0.00557542	0.0525036	intron-variant	NEB	GRCh38.p7	2:151545375	GAGGTTGGGAGTTCG[A/C]GACCAGCCTGGCCAA	4703
rs374685094	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151731657	GATGTCTAAAAATAG[C/T]CACCTCCTTTTTTAT	4703
rs374685180	snp	A/G			missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151527525	CCTGGAGGAAGTCCG[A/G]TCGGTCAGGAGTCCA	4703
rs374689143	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151577654	GGCAATCTCGGCTCA[C/T]TGCAACCTCTGCCTC	4703
rs374691148	snp	C/T	0.000458064	0.0151269	intron-variant	NEB, RIF1	GRCh38.p7	2:151490334	CATCAATGAGCTGGC[C/T]GGGTGGGACTGCCAA	4703
rs374717947	snp	A/G	1.6585e-05	0.00287962	synonymous-codon	NEB	GRCh38.p7	2:151662237	GCGGTACTTCTTTTC[A/G]CTAATAATCTCCATG	4703
rs374723803	snp	A/G	0.000169986	0.00921759	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151644474	AAATCTTACTTCACT[A/G]GCAATTTCCCGGGAG	4703
rs374727099	snp	C/G	0.000248416	0.0111421	missense	NEB	GRCh38.p7	2:151563677	TCACTTTTCCAGCCA[C/G]GTAGTGACCTTTCTG	4703
rs374734631	snp	A/G	0.00014904	0.00863121	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151633873	CTGGATCTTGGCTAC[A/G]TGCATGGACCACATC	4703
rs374735542	snp	A/G	0.159951	0.233219	intron-variant	NEB	GRCh38.p7	2:151601725	AGAGTTGCAGAACCA[A/G]ACATAGATGCAAAAG	4703
rs374740079	snp	C/T	0.000149158	0.00863464	missense	NEB	GRCh38.p7	2:151576239	TTCACCACAGGCGTC[C/T]GATAGACACTGTCAC	4703
rs374760449	snp	C/T	0.000215798	0.0103852	missense, intron-variant	NEB	GRCh38.p7	2:151627525	CTTAATTACTCACAT[C/T]GCTCTGGAGGTCATA	4703
rs374764078	snp	C/T	0.000171781	0.00926613	intron-variant	NEB	GRCh38.p7	2:151662095	TTATACCTGGATTCT[C/T]TCTGATGCATATGAA	4703
rs374776000	snp	A/G	0.0825414	0.185628	intron-variant	NEB	GRCh38.p7	2:151594749	ACATATATTCCAGTT[A/G]GGGAAAACAAGGCAC	4703
rs374776885	snp	A/G	1.6604e-05	0.00288127	intron-variant	NEB	GRCh38.p7	2:151568308	AGGCATGTGGGTGAA[A/G]CCCATACCTGGTCCA	4703
rs374795174	in-del	-/T			intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151506461	ATCTTTCCAGATCTT[-/T]AAGATTTCTTCTAAG	4703
rs374797073	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151662746	GATGACTATGGAAAC[A/C]CCATTTTTCTCTTTC	4703
rs374803216	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151619943	CACAGAATAACCCCA[C/T]AATGGTTCCTTTATA	4703
rs374805021	snp	G/T	0.0193772	0.0965046	intron-variant	NEB	GRCh38.p7	2:151649286	AAAAGTCTGTGAGGG[G/T]TTAGTTAGGAAAAGA	4703
rs374806417	snp	G/T	4.14413e-05	0.00455181	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151490375	AGGCACTTGTACCTG[G/T]TGAGACTGCAAAGAC	4703
rs374812946	snp	A/G	0.000163987	0.00905352	intron-variant	NEB	GRCh38.p7	2:151549590	TAATATGAGTCTCCT[A/G]CCACCCCACCTTCAG	4703
rs374819736	snp	A/G	7.10884e-05	0.00596147	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151526955	CTGAGGGCGAGCACC[A/G]TGTTTTTGTCATCAG	4703
rs374821601	snp	C/T	0.0170251	0.090679	intron-variant	NEB	GRCh38.p7	2:151730157	AAGGTATATCCACAT[C/T]TCAATTATTCCTATA	4703
rs374831599	snp	A/G	0.0629771	0.165899	intron-variant	NEB	GRCh38.p7	2:151606829	CAATATAAGAAAAAA[A/G]CATTCATTTCTGGGT	4703
rs374842077	snp	G/T	0.00119737	0.0244387	intron-variant	NEB, RIF1	GRCh38.p7	2:151510993	TGTAAATACTGATCT[G/T]AATTGGGGAGGAACT	4703
rs374863223	snp	C/T	2.3307e-05	0.00341365	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151630757	TGCCAACATAATCTC[C/T]GGTGTATCAGGCATT	4703
rs374864873	in-del	-/C	0.00312387	0.0393976	intron-variant	NEB	GRCh38.p7	2:151617472	AGTATATAAGCGCTA[-/C]AAAAAAAAAAAAAAA	4703
rs374866390	snp	A/G	9.96761e-05	0.0070589	intron-variant	NEB	GRCh38.p7	2:151618261	GTATCTAACAGTGAG[A/G]ATTGAAGACTCACCT	4703
rs374867405	snp	C/T	8.61453e-05	0.00656241	missense	NEB	GRCh38.p7	2:151570326	AGCGGATCTTGTTGT[C/T]ATCCCTGGCTGTGAG	4703
rs374874999	snp	A/G	0.000223228	0.0105624	synonymous-codon	NEB	GRCh38.p7	2:151562716	CAGGTCACTGAGGAT[A/G]TACTGGCACCTTTTA	4703
rs374877131	snp	A/G	4.724e-05	0.00485981	synonymous-codon	NEB	GRCh38.p7	2:151665513	GATCCCTTTCATCCA[A/G]TTGGTGAAGTCAGAT	4703
rs374879543	snp	C/T	0.0861826	0.188849	intron-variant	NEB	GRCh38.p7	2:151581318	TTGAGATGTACATTA[C/T]ACAGACACACGCAGA	4703
rs374881020	snp	C/T	1.78004e-05	0.00298327	missense	NEB	GRCh38.p7	2:151682747	CCTTTCATCCAGCTA[C/T]TGTAGTCAGCTTTGT	4703
rs374881368	snp	A/G	0.000117231	0.00765518	synonymous-codon	NEB	GRCh38.p7	2:151549666	ACGGGTGTCCTTGAT[A/G]TGTTTGAAGTGAGGA	4703
rs374883639	in-del	-/AAGTA			intron-variant	NEB	GRCh38.p7	2:151715703	CTCCAGAACTGTGAG[-/AAGTA]AAAATAAACGTCTAT	4703
rs374884826	snp	A/G	4.94976e-05	0.00497457	synonymous-codon	NEB	GRCh38.p7	2:151535742	ATTGATCGGAGAGTC[A/G]GCAACATACTTGAAA	4703
rs374904427	snp	A/C			intron-variant	NEB, RIF1	GRCh38.p7	2:151526313	TGCTGGATATCCTAC[A/C]TATTTTTATTACACC	4703
rs374908915	snp	A/C/G	5.27397e-05	0.00513493	intron-variant	NEB	GRCh38.p7	2:151640710	CTGTTTTAACTTTTA[A/C/G]TAAAAAGCAATCACT	4703
rs374917107	snp	C/T	0.000261091	0.0114227	intron-variant	NEB	GRCh38.p7	2:151612433	TAGATGTCACCTAGA[C/T]GGCCTGGTGCCTGAT	4703
rs374917890	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151728622	GAGAAATTACTATTT[A/C]TTACAGCAGGCTGTA	4703
rs374918522	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151572318	CAGAGCAAGACTCCC[A/T]CTCAAAAAATAAATA	4703
rs374929041	snp	C/T			missense	NEB	GRCh38.p7	2:151727864	CTGATTGCTCATAGT[C/T]AGATGTCCTTGTTGT	4703
rs374929094	snp	C/G/T	0.000103927	0.00720792	intron-variant	NEB	GRCh38.p7	2:151561203	AGGAGTACAGGAAGA[C/G/T]GCACCTCACTGGCAT	4703
rs374930376	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151688919	AAGACTTATGAATTG[C/T]TTGTTTCTGGAATCT	4703
rs374933570	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151666948	ATTTCAGCCCTAATA[C/T]AAATTAGTGTATTAA	4703
rs374935839	snp	A/G	1.90776e-05	0.00308844	intron-variant	NEB, RIF1	GRCh38.p7	2:151493345	TTCTTTTTAGTCCTA[A/G]AAAATACCGAGCTAA	4703
rs374938814	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151645424	AAACTTATGTTTTGA[A/C]GAAGGTTTAAATAAT	4703
rs374941096	snp	A/G	0.000115916	0.00761214	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151514397	AGGCCCTTCCCACGG[A/G]TGCTTTCCTCTAGAT	4703
rs374949827	snp	A/G	1.7402e-05	0.0029497	synonymous-codon	NEB	GRCh38.p7	2:151563841	ACTGTTCACCAGATC[A/G]GCATGCTTGGCTCCA	4703
rs374950634	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151513890	GGAGGAAACTATTCT[A/G]TGCAAGTCAGTATGG	4703
rs374957115	snp	C/T	1.73264e-05	0.00294328	synonymous-codon	NEB	GRCh38.p7	2:151552705	ACTTTTGACAGCCTG[C/T]ACGTAGACTGGTGTA	4703
rs374961597	snp	C/T	0.000116001	0.00761491	missense	NEB	GRCh38.p7	2:151538196	CTAGGGCATCTTTCA[C/T]CGTGTGGTATTTCCC	4703
rs374962220	snp	C/T	1.89672e-05	0.00307949	intron-variant	NEB	GRCh38.p7	2:151697690	AGTAGATTCCTGTCA[C/T]TCCCACGCTGATTAT	4703
rs374964721	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151552491	CCCCAGCAAACTGCT[C/T]GAATGCATCAGGTTT	4703
rs374968999	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151729829	CATCTTCACTTTGTA[A/G]TACTTCAGGAAAGCT	4703
rs374990633	snp	G/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151690130	ACTTCAACAGGGTCA[G/T]CAGGCGATTGCATGA	4703
rs375006172	snp	A/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151711279	CTTGGAGCAGAATTA[A/T]CCAAGCCAACCCCAA	4703
rs375014703	snp	A/G	0.000135398	0.00822683	synonymous-codon	NEB	GRCh38.p7	2:151656213	TGCATCTGGAAGGAG[A/G]ATGTACTTGTGAATC	4703
rs375024246	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151504672	TATTGGCCATAAACT[A/G]TTTCCCAAACTTCAC	4703
rs375026732	snp	A/C	0.000167986	0.00916322	intron-variant	NEB	GRCh38.p7	2:151629659	AGTCTATGAAAAGAA[A/C]GGCAAAGAGTTAAAG	4703
rs375040433	snp	A/G	8.28466e-05	0.00643556	synonymous-codon	NEB	GRCh38.p7	2:151554970	GAGGCACCGTGCTGT[A/G]TTCGGATCATCGTCA	4703
rs375041595	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151686715	TATCTGCAAGCTACA[C/T]TGAACATTCTCAGTA	4703
rs375047465	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151607146	CTAGCCCGCCATCTG[C/G]ATGTAAATAGAAATG	4703
rs375062057	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151664641	AAAACAACAGCATCT[C/T]GTTATTGGGGTTAGA	4703
rs375105168	snp	C/G	1.72797e-05	0.00293931	intron-variant	NEB	GRCh38.p7	2:151724994	AGTTAGAGTTCATGA[C/G]AGGCATGTACATGTG	4703
rs375112781	snp	C/G/T	5.06499e-05	0.00503218	intron-variant	NEB	GRCh38.p7	2:151627872	AAAAATAAAAATGAA[C/G/T]AGAAAGGCTTAGAAG	4703
rs375114931	snp	C/T	1.80543e-05	0.00300447	intron-variant	NEB	GRCh38.p7	2:151667787	TAGAAAGTTTCCTAC[C/T]TTTAAGTTAGACTTA	4703
rs375116982	snp	C/T	0.000248668	0.0111477	intron-variant	NEB	GRCh38.p7	2:151679889	TAAAGTCTGGACATA[C/T]GCATCAGCCCGTGAG	4703
rs375127333	snp	A/G	0.000167986	0.00916322	missense, intron-variant	NEB	GRCh38.p7	2:151616012	CTTACATCACTAGCA[A/G]TATCTCTTGAAGCCT	4703
rs375128171	snp	C/G	1.8492e-05	0.00304067	missense	NEB	GRCh38.p7	2:151694529	ACACTCACATCGCTG[C/G]TGTTCTTGGTGTTGG	4703
rs375132728	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151547208	TGAGTGATCAAGAAT[A/G]ATGGCAATTCTGTCT	4703
rs375141068	snp	G/T	0.000510148	0.0159629	intron-variant	NEB	GRCh38.p7	2:151643402	AATCATTTATCACAA[G/T]TTGTCATAATTTGTC	4703
rs375143141	snp	C/G/T	4.17731e-05	0.00457002	missense	NEB	GRCh38.p7	2:151570122	TGGCCTGAATCACAT[C/G/T]GTTCTGGTCGGGCAT	4703
rs375145370	snp	C/T	0.000142043	0.00842624	splice-acceptor-variant, intron-variant	NEB	GRCh38.p7	2:151630821	TCTGTGTATAAACGC[C/T]ATAAAAGAAGATAAG	4703
rs375150505	in-del	-/C	0.00279162	0.0372561	intron-variant	NEB	GRCh38.p7	2:151574282	CCAGGCATGTTCTTA[-/C]TCTTGAGTAATTATA	4703
rs375155384	snp	A/T	3.31246e-05	0.00406955	missense	NEB	GRCh38.p7	2:151672574	TATTCACGATCAGAC[A/T]GCAGCTTTGCCACAT	4703
rs375158508	in-del	-/G			intron-variant	NEB	GRCh38.p7	2:151723750	CTACCTGCCTTCTTT[-/G]TTTTTTTTTTTTTTT	4703
rs375160678	snp	C/T	0.00013274	0.00814571	intron-variant	NEB	GRCh38.p7	2:151626968	TTGAATGACATATAG[C/T]CCTGTCTTATTTTCC	4703
rs375164626	snp	A/G	0.000182323	0.00954611	missense, intron-variant	NEB	GRCh38.p7	2:151650298	TGATTTCCGAAGCCC[A/G]CTTGTTCTTTTCTGC	4703
rs375167899	snp	A/C/T	4.24622e-05	0.00460756	intron-variant	NEB	GRCh38.p7	2:151565711	GGAGAATAGGCTTTG[A/C/T]GTACCTGACTCATCA	4703
rs375168249	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151510375	TTTTGTTACATCCCA[A/G]CCTTTGTACAGGGAC	4703
rs375168429	snp	C/G	8.99807e-05	0.00670688	intron-variant	NEB, RIF1	GRCh38.p7	2:151533407	CATCCAAGACTTCTT[C/G]TAAACCTCCTTCTTC	4703
rs375181005	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151546077	TTGTCTTTCAAATGT[C/T]TGGCATGTGTAAGCT	4703
rs375181577	snp	A/G	3.31554e-05	0.00407144	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151519706	TTTGTAGAGCTGGCT[A/G]TCTTTTGGATTGTAT	4703
rs375182306	snp	C/T	0.000165909	0.00910643	missense	NEB	GRCh38.p7	2:151555034	TTTTCATATTCTTCC[C/T]GATATTTGATCTATA	4703
rs375186536	snp	C/T	4.11896e-05	0.00453796	intron-variant	NEB	GRCh38.p7	2:151727937	GCAGTTCAACATTGT[C/T]GTGAAAGTAAAAACT	4703
rs375199303	snp	C/T	1.73054e-05	0.00294149	intron-variant	NEB, RIF1	GRCh38.p7	2:151492361	CTGACAGGCAGCCAG[C/T]CAATCCTAAAGAATT	4703
rs375200998	snp	C/G/T	0.000125383	0.00791697	intron-variant	NEB	GRCh38.p7	2:151697099	ACATATCCTGACCAC[C/G/T]AGATGCTATGGAAGG	4703
rs375216341	snp	C/G/T	0.000163987	0.00905353	intron-variant	NEB, RIF1	GRCh38.p7	2:151513556	TACTTTCCTGAAAGA[C/G/T]TGACATCGAATAGTA	4703
rs375216659	snp	A/C/G	6.62442e-05	0.00575485	missense, intron-variant	NEB	GRCh38.p7	2:151633914	CATCTTCAATGTTCC[A/C/G]GGCTCCAATATGGTG	4703
rs375216853	snp	G/T	3.31318e-05	0.00406999	missense, intron-variant	NEB	GRCh38.p7	2:151644502	GAGGCTTTTGCTGCT[G/T]TGATTGGTATGGCAT	4703
rs375244873	in-del	-/AAGA			intron-variant	NEB, RIF1	GRCh38.p7	2:151508533	GTTAAGAGTCAAAGA[-/AAGA]CATGACCTCTAGAAA	4703
rs375249117	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151567838	AAGAATTTGAACAAT[C/T]GCTTTTAAAAAAGCC	4703
rs375256600	snp	A/C/G	0.000103714	0.0072005	missense	NEB	GRCh38.p7	2:151656199	AGCTCAATGTTCATT[A/C/G]CATCTGGAAGGAGGA	4703
rs375261614	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151704042	GATGGGTTTTTGGTG[C/T]GGATGTCCTTTCTGT	4703
rs375265096	snp	A/G	7.60196e-05	0.00616474	intron-variant	NEB	GRCh38.p7	2:151690703	CTCTGGGTCACCCAC[A/G]CTTGCATAAATCAAA	4703
rs375266824	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151726394	TAGAATTTTACCAAA[C/G]AGTGAGCTGCTATCA	4703
rs375279588	in-del	-/GT			intron-variant	NEB, RIF1	GRCh38.p7	2:151524480	CCTTGGCAATGGCTG[-/GT]TTGGGGACTGGGGAC	4703
rs375289058	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151712150	ATCTCCTAATGCATC[A/C]TTTTTTGGAGAGACA	4703
rs375292986	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151663973	GAGCTACTCTAAAAT[G/T]GGAAGGGAGGCACTC	4703
rs375293033	snp	A/G	0.000181439	0.00952294	intron-variant	NEB	GRCh38.p7	2:151619403	AGAACTCACAGACAC[A/G]TTTCAGATCCGCTTT	4703
rs375294508	snp	C/T	0.000132499	0.00813829	missense	NEB	GRCh38.p7	2:151575724	GAGCATTTGCTCTAG[C/T]GAGATTAATTTCTGG	4703
rs375298473	snp	C/T	0.00159617	0.0282053	upstream-variant-2KB	NEB	GRCh38.p7	2:151735201	GGCTCCCAGAAGCAA[C/T]GTGTGAATGCGGACA	4703
rs375304669	snp	A/G	0.00034825	0.013191	intron-variant	NEB	GRCh38.p7	2:151563582	TGGGGCACAAATCCC[A/G]TGTTAAAGTGGACAT	4703
rs375307136	snp	C/T	3.33444e-05	0.00408303	missense	NEB	GRCh38.p7	2:151551769	TATGCATGAAGGGCC[C/T]GGTCCAGATCCACGG	4703
rs375312685	snp	A/G	0.000239055	0.0109302	intron-variant	NEB	GRCh38.p7	2:151537989	TATCTGTTATAAAAA[A/G]CACAAAGACAGCTGT	4703
rs375313114	snp	A/G	0.000161987	0.00899817	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151640544	CTCAAAGTCCTTCTT[A/G]TACTCCCTGTCACTC	4703
rs375313248	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151704546	CTCCGAGCCAGGTGC[A/G]GGATATAATCTCGTG	4703
rs375322569	snp	A/G	0.000106779	0.00730602	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151516520	GTTTCAAAGTCCAGC[A/G]TGGGTTTTCCTCGTT	4703
rs375345535	in-del	-/ATT	0.0189856	0.0955633	intron-variant	NEB	GRCh38.p7	2:151545281	AAAATAATAAGTAAA[-/ATT]ATTATTTCTAGGCCA	4703
rs375357016	snp	A/G	8.28397e-05	0.00643529	missense	NEB	GRCh38.p7	2:151563607	GGACATTTACTTACC[A/G]CACTCCTCATCTTTT	4703
rs375377794	snp	C/T			intron-variant, missense	NEB, RIF1	GRCh38.p7	2:151533542	GCACTAGATTTATAT[C/T]TTCTCTGTCCATGCA	4703
rs375383335	snp	G/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151487153	GAGGTCAGTCTTGTA[G/T]TTTAGAGAAGAATTT	4703
rs375386622	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151552190	CTGCTTTGTGTCAGG[C/T]GTCATAGTGGGTGCT	4703
rs375389456	snp	C/T	0.00159617	0.0282053	intron-variant	NEB, RIF1	GRCh38.p7	2:151522894	CACACACAGCTGAAG[C/T]GCCCTTGGGCCCAGG	4703
rs375407146	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151639523	TTTTATGCACATCTT[C/T]GGGTAATAAGTTCAT	4703
rs375409868	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151717855	TATACCTCCTTTGTT[C/T]TTTTTTTTTTTTTTT	4703
rs375412223	snp	A/G	0.000533627	0.0163257	missense	NEB	GRCh38.p7	2:151662166	GCATTATTCTGGGCC[A/G]AAACCATGTTCATCG	4703
rs375434588	snp	A/G	6.63724e-05	0.00576036	synonymous-codon	NEB	GRCh38.p7	2:151576214	GTCAACAATGCTTGT[A/G]TACTTAAGGTTCACC	4703
rs375442628	snp	A/C/T	0.000199938	0.00999657	intron-variant	NEB, RIF1	GRCh38.p7	2:151525129	TTCCACTGCTTCAAA[A/C/T]GGGCCCCCAAGAGTG	4703
rs375458245	snp	G/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151505830	CTGCAGCCCTTTCCT[G/T]TATACTCCAATGTCT	4703
rs375470527	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151645197	GAAATGGATTATTAT[C/T]GAGGTGCTGTTTTTC	4703
rs375483860	snp	C/T	0.0314385	0.121371	intron-variant	NEB	GRCh38.p7	2:151605854	TTGCCCAGGCTGGAA[C/T]GCAATGGCATGATCT	4703
rs375502035	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151567596	GCTTTTTGTTTGACA[C/T]CCCCAACTCTGAGAG	4703
rs375504512	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151567000	TAGGCAAACCAATCA[A/G]TCCATCACTGCTCCT	4703
rs375506991	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151708861	AACCCGTGTCATCCA[A/G]TCCATCAGCAAATCA	4703
rs375510817	snp	C/T	3.31279e-05	0.00406975	missense	NEB	GRCh38.p7	2:151687466	GCAGCATCTTTGGAT[C/T]GTCATTAATGCTGAG	4703
rs375533560	snp	C/G	0.000182429	0.00954888	intron-variant	NEB	GRCh38.p7	2:151729597	ATGCAGTTTATGCAG[C/G]TGTGGGCTGGGCCTT	4703
rs375534633	snp	A/G	0.000161987	0.00899818	synonymous-codon	NEB	GRCh38.p7	2:151570186	CATGTCACTGACCAG[A/G]GCCTGGGAATTTTTA	4703
rs375543045	snp	A/G	0.00062614	0.0176827	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151625552	ACTATAATTTATTTT[A/G]TTTTGTCTTGCCAAC	4703
rs375545766	snp	C/T	1.65767e-05	0.00287891	missense	NEB	GRCh38.p7	2:151548375	GGGCCAAGTGTATAC[C/T]CATATGCCTTGGTGT	4703
rs375552682	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151628639	TGAGGTCAGGAGTTT[C/G]AGACCAGCCTAGCCA	4703
rs375569766	snp	C/T	0.000182374	0.00954746	synonymous-codon	NEB	GRCh38.p7	2:151677999	CTGGGCTTTCTTAGC[C/T]GCCACGACATTGAAC	4703
rs375573462	snp	C/T	2.24298e-05	0.00334879	intron-variant	NEB	GRCh38.p7	2:151717568	AAACGATTATGCTTT[C/T]ATCTTTATTTGAAGT	4703
rs375580202	in-del	-/ACAA			intron-variant	NEB, RIF1	GRCh38.p7	2:151509167	AGAGACAACAAACAA[-/ACAA]GCAGTTTCAGCCAAT	4703
rs375581714	snp	C/T	3.64014e-05	0.00426607	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151527523	AGCCTGGAGGAAGTC[C/T]GGTCGGTCAGGAGTC	4703
rs375588361	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151685879	AAGTACAGATGTGCA[C/T]TACAAATCTTCTGTA	4703
rs375622138	snp	A/G	1.65817e-05	0.00287933	intron-variant	NEB	GRCh38.p7	2:151729689	AGGCATTGGCAAGAG[A/G]ACCAAAGCAGAAACC	4703
rs375628303	snp	A/C/G/T	5.02656e-05	0.00501307	splice-donor-variant	NEB	GRCh38.p7	2:151679720	CCACAGCTGGACTTA[A/C/G/T]GTCACTCGCCGCCTG	4703
rs375646776	snp	A/G	7.72096e-05	0.0062128	missense	NEB	GRCh38.p7	2:151552763	GTTTTCAACATGTGA[A/G]CTTTATACTTGATCT	4703
rs375655424	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151644723	AAATTATGCCCATTG[A/G]TTGCTAATGATCCTG	4703
rs375657086	snp	A/C/T	3.76777e-05	0.00434024	missense, intron-variant	NEB	GRCh38.p7	2:151616070	GACGCAAGTCATAGC[A/C/T]TTCCTTCTTGGACTC	4703
rs375657266	snp	C/T	0.000163987	0.00905353	missense, intron-variant	NEB	GRCh38.p7	2:151629591	ATGGGGATGGCGTCA[C/T]TTCGCAAGTCGTAGC	4703
rs375674948	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151648918	AGGACCCCAGCTGGC[C/T]CGGGTTTTGTGTGGC	4703
rs375705906	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151492716	CGAAAATGAAACTCA[C/T]TTTCAAAGAAGGGGC	4703
rs375710037	snp	A/C	0.000163986	0.00905352	synonymous-codon	NEB	GRCh38.p7	2:151688337	TTGGATAAACTGTGG[A/C]GCATCTGCTGGTATA	4703
rs375720162	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151499992	AGGATCATTAAGGTT[C/T]CAAATAGATACAAAT	4703
rs375721498	snp	A/G	1.65608e-05	0.00287752	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151640412	GCTCTGGTCGGGCAG[A/G]CATGTCCACTGGTGC	4703
rs375723442	snp	A/G	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151542791	TTTTCTTAATGCTCA[A/G]ATCTATTCTTCATAG	4703
rs375723456	snp	A/G	0.000442788	0.0148727	intron-variant	NEB	GRCh38.p7	2:151655260	AAAATTAATTTTTAT[A/G]TAAATTTACCTGACT	4703
rs375731546	snp	C/T	0.00018339	0.00957399	intron-variant	NEB	GRCh38.p7	2:151627220	TCTGGAGAGATTAAA[C/T]ACAAAAGCGAGTATT	4703
rs375737365	snp	C/G/T	0.000268323	0.0115798	missense	NEB	GRCh38.p7	2:151695630	AAAGCAGGAGTATCA[C/G/T]GGGGGATATGGCACT	4703
rs375749306	snp	A/G	0.000182896	0.00956109	synonymous-codon	NEB	GRCh38.p7	2:151727730	CTGACTGTGTGCAAT[A/G]TAGGGGGTCATGAAC	4703
rs375756148	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151726772	GGCTTATGCCTATAA[G/T]TCTAATGTTTTGTGG	4703
rs375763991	snp	A/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151518089	AAAACACACTCTTTA[A/T]GCTTCCAGCCCCTGC	4703
rs375768742	snp	C/T	2.36897e-05	0.00344155	intron-variant	NEB	GRCh38.p7	2:151547563	ATACCCCAAAACATA[C/T]GTATTAGAGACCGAA	4703
rs375771207	snp	A/G/T	1.96423e-05	0.00313381	intron-variant	NEB	GRCh38.p7	2:151680058	TAAACAAACAAATAA[A/G/T]GTAGAAAGAAAATTT	4703
rs375774380	snp	A/C/T	4.71879e-05	0.00485717	intron-variant	NEB	GRCh38.p7	2:151662105	ATTCTCTCTGATGCA[A/C/T]ATGAAACACTGCATT	4703
rs375777350	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151656769	CAGATTTTGTGATGA[C/T]GCATCACACTGACTT	4703
rs375780147	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151701831	GCTCCTGGATTCATT[A/G]ATTTTTTGAAGGGTT	4703
rs375796482	snp	C/T	0.000163987	0.00905353	missense, intron-variant	NEB	GRCh38.p7	2:151644042	TCTTGGCCACATGCA[C/T]GGACCACATCATCTT	4703
rs375807681	snp	A/C			intron-variant	NEB, RIF1	GRCh38.p7	2:151496492	GGAGCCAGAAGTTAT[A/C]TGCTGACAAAATGCC	4703
rs375811851	snp	C/T	1.65891e-05	0.00287998	missense, intron-variant	NEB	GRCh38.p7	2:151633695	GAGCATGGATGACAT[C/T]GCTCTGGTCAGGCAG	4703
rs375814899	snp	A/G	0.00013326	0.00816163	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151619502	GATGTCATTCTGGTC[A/G]GGCAGGCAGATCCAT	4703
rs375817279	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151489734	ACCAATGAGCCAAAA[C/T]TGATGCTTTGCTCTA	4703
rs375829957	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151701673	TGTTTGTAGTATTCT[C/T]TGATGGTAGTTTGTA	4703
rs375830667	snp	C/T	8.27986e-05	0.0064337	missense, intron-variant	NEB	GRCh38.p7	2:151627661	TAACACCACTCCCAG[C/T]ATGTCCACTGGGCTG	4703
rs375837416	snp	C/T	0.000104586	0.00723064	missense	NEB	GRCh38.p7	2:151568671	AATCAACTCTGTCAT[C/T]CACAGGCGTAAAGTT	4703
rs375843338	snp	C/T	4.97071e-05	0.00498509	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151525183	TTTGCTTCTTGGCCA[C/T]TTCCATAGCATGTTT	4703
rs375851843	snp	C/T	4.51651e-05	0.00475189	intron-variant	NEB	GRCh38.p7	2:151547575	ATATGTATTAGAGAC[C/T]GAATGATTAACATTC	4703
rs375877485	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151704720	GCCCTGCTTCGGCTC[A/C]CGCACAGTGCGAGCA	4703
rs375883374	in-del	-/A	0.00478085	0.0486577	intron-variant	NEB	GRCh38.p7	2:151652696	TTTCTGAAAATTTAT[-/A]AATACAAGGACATTT	4703
rs375888522	snp	C/T	0.000108909	0.00737852	intron-variant	NEB	GRCh38.p7	2:151696606	TGTTATCCCTCATAA[C/T]TGGGTGTCCTGAGTA	4703
rs375894183	snp	C/T	0.000364353	0.0134924	missense	NEB	GRCh38.p7	2:151687516	TTGCTCTTTTCATAG[C/T]CTTTCTTGTACATCA	4703
rs375909006	snp	A/G	0.000282357	0.0118785	missense	NEB	GRCh38.p7	2:151727791	TTCCTCCTCTCCACC[A/G]GCTTTGCTGATGCTG	4703
rs375936460	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151664185	TTTCTCATGGTGCAT[C/T]TTTAAAGAGAGGGCC	4703
rs375938655	snp	A/G	4.03364e-05	0.00449072	missense	NEB	GRCh38.p7	2:151562667	TGGGTTCTTCCAGAA[A/G]AGACGTCCACTGGTG	4703
rs375957418	in-del	-/A	0.00119737	0.0244387	intron-variant	NEB, RIF1	GRCh38.p7	2:151510196	CAGGGAGGTTTGAGG[-/A]GTTTCTTCAGACCCC	4703
rs375966356	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151520251	TTTAAAATAGTACTT[C/T]GGCTATATCATTTAA	4703
rs375977317	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151606944	GTTTGAATATTTGCA[C/T]CCATCACAATATGGT	4703
rs375986600	snp	C/T	0.000167986	0.00916323	intron-variant	NEB	GRCh38.p7	2:151657967	CCAGCCAGGTGACCG[C/T]TTCCTTTGGACTTAC	4703
rs375987922	snp	C/T	0.00398564	0.0444627	intron-variant	NEB	GRCh38.p7	2:151612850	GTGTTTTTTTGGGGA[C/T]AAAAACGACGTCTTT	4703
rs375992994	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151641862	GTACATGTGCACAAC[A/G]TGCAGGTTTGTTACA	4703
rs375997049	snp	A/G	4.97154e-05	0.0049855	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151639947	GTCTGGAGGCTGGCG[A/G]TAGATTTTATCACTC	4703
rs376008654	snp	G/T	1.65784e-05	0.00287905	synonymous-codon	NEB	GRCh38.p7	2:151697196	ATATTCTTGAGTTAT[G/T]GTCTGAGGGAAGAAG	4703
rs376013221	snp	G/T	3.70185e-05	0.00430208	missense	NEB	GRCh38.p7	2:151672370	TTACACATACTTACA[G/T]CACTCTGAATTTGAT	4703
rs376019368	snp	C/G/T	4.97742e-05	0.00498849	missense, intron-variant	NEB	GRCh38.p7	2:151609891	TCATGCAGGTAATTG[C/G/T]GATAATCAATGTCAG	4703
rs376037403	snp	A/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151504359	CCAACAAAGCAGCAG[A/T]ATTGATCTCGGACAA	4703
rs376045753	snp	A/G	6.12689e-05	0.0055345	intron-variant	NEB, RIF1	GRCh38.p7	2:151491804	CAGTGATCAGAACAA[A/G]TGTTCTTGGAGTTTT	4703
rs376065596	snp	C/T	0.000465908	0.0152557	intron-variant	NEB, RIF1	GRCh38.p7	2:151508122	TTTCTGGGAATAGAT[C/T]CCAAGAAATAAGGAG	4703
rs376072545	snp	A/G	7.52078e-05	0.00613174	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151527004	CCTTGAGGAACTCCC[A/G]GTCCAGCTTATATTC	4703
rs376082951	snp	C/T	8.28974e-05	0.00643753	intron-variant	NEB, RIF1	GRCh38.p7	2:151489925	TCATGTTTGCACATA[C/T]CAAAAATTAAGAATA	4703
rs376085885	snp	C/T	3.31592e-05	0.00407167	intron-variant	NEB	GRCh38.p7	2:151729609	CAGCTGTGGGCTGGG[C/T]CTTACCTCTCCCGGC	4703
rs376091169	in-del	-/A	0.00438332	0.0466095	intron-variant	NEB	GRCh38.p7	2:151640240	CCTGTCGATAAAGGC[-/A]ATGCTATTTGCCTCC	4703
rs376099069	snp	A/G	0.00438332	0.0466095	intron-variant	NEB, RIF1	GRCh38.p7	2:151511174	TGGTGAGGCTCTCAC[A/G]GCCCAAAGAATATCA	4703
rs376101302	snp	C/T	1.65619e-05	0.00287762	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151524376	CGAGCATGCTTAAGC[C/T]ATGGCTGCCTTCCTT	4703
rs376120080	snp	A/G	0.000167986	0.00916323	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151614579	GCGGTAGCCTTCCTT[A/G]TACTTGTACTAAAAA	4703
rs376129412	snp	C/T	0.000754561	0.019409	intron-variant	NEB	GRCh38.p7	2:151562594	AGCTGAGTCAAGCTG[C/T]AGAAGGGACATCATA	4703
rs376144975	snp	A/G	0.000167986	0.00916323	intron-variant	NEB, RIF1	GRCh38.p7	2:151514774	AGTGTCACTAGTGCA[A/G]TTATTTGGATTAAGA	4703
rs376148882	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151681146	CTGGAAACATCACAG[A/G]GTTTTCTAAAGGTTT	4703
rs376152166	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151658850	CCTAGAACAAAATCC[A/C]ATCACACCGTTCAAA	4703
rs376152685	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151732177	CCTCCAAGTGCCTTA[G/T]GCATTTGGAGATTTT	4703
rs376157878	snp	A/G	0.000165266	0.00908878	missense	NEB	GRCh38.p7	2:151540402	GGCGTATCTGGAACC[A/G]GAGTGTACTTGTCTT	4703
rs376163240	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151616740	ATTATTGTCATCATA[A/G]TATAAAAGACACAGC	4703
rs376182104	snp	A/G	9.94151e-05	0.00704966	missense, intron-variant	NEB	GRCh38.p7	2:151627168	ATGGGGACCCAGCCA[A/G]TGCCTCTCAGCCACT	4703
rs376187503	snp	A/G	0.000146854	0.00856769	intron-variant	NEB	GRCh38.p7	2:151709785	GACATCAGACAAGCT[A/G]AAGAACTGCTGTGGA	4703
rs376194864	snp	C/T	0.00018259	0.0095531	missense, intron-variant	NEB	GRCh38.p7	2:151610772	CTTACTTGGCTGATA[C/T]TGGCAGAATTACTCT	4703
rs376199241	snp	C/T	0.000202211	0.0100531	synonymous-codon	NEB	GRCh38.p7	2:151568077	ATGTATTACCTCACT[C/T]TGAACGTCATTGCAG	4703
rs376200575	snp	A/G	0.000155318	0.00881108	intron-variant	NEB	GRCh38.p7	2:151555090	GTTTTAGAGAGTAAT[A/G]GATTTATATTATTAA	4703
rs376205959	snp	C/T	4.98907e-05	0.00499428	intron-variant	NEB	GRCh38.p7	2:151546466	GCAAACACAGAAATA[C/T]AGCTGGTCATAAGCA	4703
rs376210839	snp	A/G	1.65685e-05	0.00287819	synonymous-codon	NEB	GRCh38.p7	2:151679939	GATATTGTAGGCATT[A/G]ACTTTAGCCTGGATG	4703
rs376215599	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151500423	CAGAGTTGTATATAA[C/T]ACACAAATAATTTGT	4703
rs376218705	snp	A/T	8.29208e-05	0.00643844	intron-variant	NEB	GRCh38.p7	2:151659023	TCTTACTGGTTCAAA[A/T]CTGCTGGAGAGAAAG	4703
rs376221776	snp	A/G	0.000437904	0.0147905	synonymous-codon, intron-variant, utr-variant-3-prime	NEB, RIF1	GRCh38.p7	2:151497710	GCCCATGTTTTCTTT[A/G]TATAACACCTGTGCG	4703
rs376224722	snp	C/T	3.31362e-05	0.00407026	missense, intron-variant	NEB	GRCh38.p7	2:151631244	GGCGGTAGATGTTAT[C/T]ACTCAGTATTTCGGT	4703
rs376233306	snp	A/G	5.40921e-05	0.0052003	intron-variant	NEB, RIF1	GRCh38.p7	2:151527459	TATGCAGTTACAATC[A/G]TCTGTGTCTCTCCTG	4703
rs376248833	snp	C/T	3.31351e-05	0.00407019	intron-variant	NEB	GRCh38.p7	2:151575663	GACTGGGTAACTTTC[C/T]AAACAAAAAGAGAGT	4703
rs376262701	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151612709	TGATGGTCCCTACCT[C/T]CTCTTATGGAAACTG	4703
rs376268872	snp	A/G	0.000132608	0.00814166	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151614315	CCGAGCCTGAATGAC[A/G]TCATTCTGATCAGGC	4703
rs376277385	snp	C/T	9.95091e-05	0.00705299	missense	NEB	GRCh38.p7	2:151569285	CACTGAAGATGTCCG[C/T]GGCATGTTTGGCATG	4703
rs376281958	snp	A/G	0.000231562	0.0107577	intron-variant	NEB	GRCh38.p7	2:151561343	AAAGTCATCAAAAAT[A/G]GTAACATACAGGTCT	4703
rs376283107	in-del	-/T			intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151497281	GAGTTATCCATGTTA[-/T]TTTTTTTTTTTCCTT	4703
rs376288418	snp	C/T	4.99313e-05	0.00499632	missense	NEB	GRCh38.p7	2:151724916	TTGCTTTTTCATCTA[C/T]GTGACATATAGTCTT	4703
rs376290032	in-del	CTTAA/T			intron-variant	NEB	GRCh38.p7	2:151713598	CCTGAAATCTCATAT[CTTAA/T]TTTTCTTTTGTGGAT	4703
rs376355410	snp	G/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151486382	TGTGGAGAAATTGGG[G/T]CCTTCATAAACCACT	4703
rs376370460	snp	A/G	0.000123993	0.0078728	intron-variant	NEB	GRCh38.p7	2:151567485	TGTATTTCAGCTGGC[A/G]AGAAGAGGAATATAA	4703
rs376394584	snp	C/T	0.000167986	0.00916322	missense	NEB	GRCh38.p7	2:151697606	TCTCGCAGTAATTTA[C/T]GCTCTTTGCTTTTGT	4703
rs376429348	snp	C/T	0.000165986	0.00910854	intron-variant	NEB	GRCh38.p7	2:151674468	ACTTCACCTAAAATT[C/T]GTACTCACATCACTG	4703
rs376465215	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151629790	GTGGAAAGCAAATAA[A/T]TTATATTCTACCAAA	4703
rs376478761	snp	C/T	0.000215448	0.0103768	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151493775	TCCTTTCTAAAATAC[C/T]GAGCTAAAGTTTTCT	4703
rs376494214	snp	C/T	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151549030	TCAACTGGGACTTGA[C/T]GCATTTACCCCATGG	4703
rs376495046	snp	C/T	3.31857e-05	0.00407329	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151519744	TCTTGCCCTTTTCTT[C/T]ATCGAAATTTTCTCG	4703
rs376501860	in-del	-/T	3.53139e-05	0.00420187	utr-variant-3-prime, intron-variant	NEB, RIF1	GRCh38.p7	2:151485724	TGACTGCAGGATCTG[-/T]TAAGTCCTGCAGACA	4703
rs376503299	snp	A/G/T	7.94446e-05	0.00630215	missense	NEB	GRCh38.p7	2:151691920	GTGTTATTGTCTGAG[A/G/T]GAAATAGCATTTTCC	4703
rs376503933	in-del	-/GGC			intron-variant	NEB	GRCh38.p7	2:151717389	GAGTCTTCAAGGGAG[-/GGC]GCAATGTCCCAGCTC	4703
rs376507321	snp	A/T	8.28617e-05	0.00643615	intron-variant	NEB, RIF1	GRCh38.p7	2:151506127	TAAATTATCAAAGGG[A/T]GGCAGAAAATATTGC	4703
rs376507810	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151566460	CTATGCTGCAGCAGT[C/T]TTTGACTTCCAGGTT	4703
rs376511134	snp	C/T	0.000967534	0.0219734	NEB	2	allele_origin=T(germline)/C(germline)	2:151675279	ATCCCAGCAAAGACC[C/T]TACTTACGTCACTTA	4703
rs376512820	snp	A/G	9.98552e-05	0.00706524	synonymous-codon	NEB	GRCh38.p7	2:151677924	CTCCAGGTCCATGGC[A/G]TCAGGCAAGTAGGTG	4703
rs376524766	snp	A/G	0.000116054	0.00761668	synonymous-codon	NEB	GRCh38.p7	2:151678008	CTTAGCCGCCACGAC[A/G]TTGAACATATCATGG	4703
rs376534942	snp	A/G	0.00046433	0.0152299	intron-variant	NEB	GRCh38.p7	2:151692031	AACAATGTCACTGTG[A/G]GGCATGAACCATTGT	4703
rs376535906	snp	A/G	8.30392e-05	0.00644304	synonymous-codon	NEB	GRCh38.p7	2:151656006	GTACCATTCATTGTA[A/G]TCTTGCTTATATTCA	4703
rs376540186	snp	C/T	1.79464e-05	0.00299548	intron-variant	NEB	GRCh38.p7	2:151666044	GGCTCCTGTTTTTTC[C/T]TCCCACCCATTAGAA	4703
rs376558062	snp	C/T	4.97137e-05	0.00498542	missense, intron-variant	NEB	GRCh38.p7	2:151619647	TCTTTCTTGTACTCA[C/T]GGTCACTCTGCACTT	4703
rs376559033	in-del	-/A	0.0325976	0.123435	intron-variant	NEB	GRCh38.p7	2:151556938	TAAAACTGACACCCT[-/A]ACATCACAATTAAAA	4703
rs376580237	snp	C/T	1.65847e-05	0.0028796	missense	NEB	GRCh38.p7	2:151538235	TTTGAAATGTTTCTT[C/T]GTAGCGTAGCTAGAA	4703
rs376597690	snp	A/G	1.69729e-05	0.0029131	synonymous-codon	NEB	GRCh38.p7	2:151695578	GCATAAGGAACTTAC[A/G]TCACTCAAGTTATAG	4703
rs376609115	snp	A/G	4.9736e-05	0.00498653	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151519713	AGCTGGCTGTCTTTT[A/G]GATTGTATTTTGGTG	4703
rs376611641	snp	A/C	6.62954e-05	0.00575702	missense	NEB	GRCh38.p7	2:151674500	CAATGTTTCTCGATG[A/C]CTTGGCTGCAGTGAT	4703
rs376614443	snp	C/T	0.000165986	0.00910855	missense	NEB	GRCh38.p7	2:151694343	TCTGGTTTTTGGCCA[C/T]CTTCAAGGAGTGCAG	4703
rs376616601	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151544615	GGCTGAAATAACACA[A/G]TGAAGCTTTTAGGAA	4703
rs376617021	snp	A/C/T	5.11758e-05	0.00505819	intron-variant	NEB	GRCh38.p7	2:151662367	GGAAAAATTAAATTA[A/C/T]GAGAAGAAACTGGAA	4703
rs376621580	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151711419	GCCTACATCCCCACA[A/G]TACCCTTTAAGGAAA	4703
rs376623225	snp	C/T	0.000134003	0.00818436	intron-variant	NEB	GRCh38.p7	2:151663863	CTTGTATTTGTACTG[C/T]GGACAGAGAAGAAAT	4703
rs376626113	snp	A/G	0.000167986	0.00916322	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151654004	CACATCACTAGCAAT[A/G]TCTCTTGAAGCTTTA	4703
rs376626620	snp	C/T	6.83142e-05	0.00584401	missense	NEB	GRCh38.p7	2:151724859	ATCATTGCCTTACCT[C/T]ACTGACTTGCTGCGA	4703
rs376630715	snp	C/T	0.000165986	0.00910854	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151640037	AATGCCTCTCATCCA[C/T]TGGAGATCAGACTTG	4703
rs376636477	snp	C/G	0.000167986	0.00916323	intron-variant	NEB	GRCh38.p7	2:151650907	TCAGAGAAAACACAG[C/G]TCTTTTAGTACACAA	4703
rs376636568	snp	A/C/T	1.6588e-05	0.00287988	synonymous-codon, missense	NEB	GRCh38.p7	2:151679736	GTCACTCGCCGCCTG[A/C/T]CTGGCAGCTTTGGCA	4703
rs376655029	snp	C/T	0.000195155	0.0098762	synonymous-codon	NEB	GRCh38.p7	2:151567426	ATCATCTCTCATCGT[C/T]GGGACACCAACATAA	4703
rs376658336	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151719815	GCCTGGGAGGTGGAG[A/G]TTGCAATAAGCCAAT	4703
rs376664167	snp	A/C	0.000161329	0.0089799	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151493824	TCCATCTCAGGAGTA[A/C]AGGGTGTGGGGGTTG	4703
rs376674974	snp	C/T	0.00755907	0.0610114	intron-variant	NEB	GRCh38.p7	2:151729111	ATTTATGGTAATAGG[C/T]TATTTAGAATTGCTA	4703
rs376680564	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151689345	CAGTAGCTGAGACTA[C/T]AGGCATGTGCCACCA	4703
rs376684415	snp	C/T	1.65616e-05	0.00287759	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151526028	AGTGTTGTGTATGAG[C/T]CCTGTGCCAAGTGCT	4703
rs376693617	snp	A/C	2.77204e-05	0.00372283	missense	NEB	GRCh38.p7	2:151664592	TTTTCCTCTTCCCAG[A/C]CAGCTTTGTACAGTT	4703
rs376710012	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151541557	TGTAGACCAGCTAGA[C/T]ATAAACCAAGTTATC	4703
rs376713799	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151684090	GGGAGTTGCTGTTTA[A/G]TGAATACAGAATTTC	4703
rs376718485	snp	C/T	0.206947	0.246265	intron-variant	NEB	GRCh38.p7	2:151584236	ATCTCCATCACCAAG[C/T]TTCCCTGACAAGTGC	4703
rs376723012	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151641094	ATTCTAGATAAGTAC[C/T]GCAGATTCAATAAAA	4703
rs376726354	snp	A/C/T	8.28118e-05	0.0064343	missense, intron-variant	NEB	GRCh38.p7	2:151631231	TTGTCCGGAGGCTGG[A/C/T]GGTAGATGTTATCAC	4703
rs376732812	snp	C/T	0.000110871	0.00744467	missense	NEB	GRCh38.p7	2:151562769	CATTGGGGATATGAA[C/T]ATTTGCTTTGGTATC	4703
rs376741337	snp	A/G	1.67604e-05	0.00289481	synonymous-codon	NEB	GRCh38.p7	2:151537150	GCTGTAGAGAGTCTT[A/G]TTCTTTTCAGCCAGA	4703
rs376759078	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151688214	ATTTGCACAATTCCT[C/T]GTCTTGTCTTTTAAA	4703
rs376769059	snp	C/G	0.000437904	0.0147905	intron-variant	NEB	GRCh38.p7	2:151636385	TTATATCTAAAAACT[C/G]ACAGAGGACTAAGAC	4703
rs376788015	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151560305	TGTCTTCAGCCCATC[C/T]TTACTTCTGACTCTA	4703
rs376788751	snp	A/C	1.66832e-05	0.00288814	intron-variant	NEB, RIF1	GRCh38.p7	2:151492501	ATAAAGAACCTGATG[A/C]AGGAGAGACCGTGAA	4703
rs376798329	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151646277	TGGTGTTGTTAGATT[A/T]GTGAATGATACAGTT	4703
rs376799101	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151634539	CCCAGCTACTTGGGA[A/G]GCTGAGGCAGGAGAA	4703
rs376818553	in-del	-/G			intron-variant	NEB	GRCh38.p7	2:151679291	CTGGCTATTACAGGT[-/G]GGTGAAATTGAGGCC	4703
rs376827489	in-del	-/T			intron-variant	NEB	GRCh38.p7	2:151561572	ACAGCAGCCCCTCAC[-/T]TTTTTTTTTTTTTTG	4703
rs376835458	snp	A/G	8.32106e-05	0.00644968	missense	NEB	GRCh38.p7	2:151717477	GGATCAGCCAGAGGC[A/G]TGAATTGAGCTTGCT	4703
rs376849181	snp	C/T	0.000103271	0.00718503	synonymous-codon	NEB	GRCh38.p7	2:151684790	CACATCGCTCTGCAG[C/T]GCATATGCCTTCTTG	4703
rs376859839	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151563343	CTTTTATAACACAGG[G/T]TAAATAGTGACCTTG	4703
rs376866297	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151701528	TAAACTATTGATTAT[C/T]GCCACAATTTCAGCT	4703
rs376869270	snp	A/G	9.85309e-05	0.00701824	intron-variant	NEB	GRCh38.p7	2:151547743	CGATACAGTCTCTAC[A/G]TTGGAGGAAATATCA	4703
rs376876225	in-del	-/A			intron-variant	NEB	GRCh38.p7	2:151697773	TCAACTGTCTTAAAA[-/A]CTGACAATTGAGGCC	4703
rs376890655	snp	C/G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151640729	AAAGCAATCACTAAG[C/G/T]CTAACTTGCTCTATT	4703
rs376897146	snp	C/T	0.00048607	0.015582	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151490508	CTCCCGGCTCCGGCG[C/T]TGAGCTTGGACTGGG	4703
rs376904705	snp	C/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151531448	CAGCCTCCTGAGTAG[C/G]TGGGACCACAGGCAT	4703
rs376911383	snp	A/G	9.94497e-05	0.00705088	synonymous-codon	NEB	GRCh38.p7	2:151697232	GCCTCTGTCTTCTTC[A/G]TATTCTGCTTTGTAG	4703
rs376913159	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151674915	ATGAAAGGAATGTCA[A/T]GAGAAGACCTGGTGG	4703
rs376932516	snp	C/T	0.000115964	0.00761371	missense, intron-variant	NEB	GRCh38.p7	2:151627812	TGGCCGAGCTGCTTG[C/T]GGTAACCATCTTTGT	4703
rs376953361	snp	G/T	9.13534e-05	0.00675784	intron-variant, missense, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151498245	GGCATTTTTTCCCCT[G/T]TCTTTCCAAAATACC	4703
rs376973987	snp	C/T	1.70127e-05	0.00291652	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151492410	TGTGCCGTTGGGTCT[C/T]CCTCACCCGTCTCAT	4703
rs376977065	snp	G/T	0.000167986	0.00916323	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151513675	TGACTTCCAGTTCCA[G/T]GTCTCGCTTATATTC	4703
rs376984481	snp	C/G/T	0.000132489	0.00813815	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151489985	CTCCAGCAGTAGATG[C/G/T]ATGAGATGGGATGGA	4703
rs376988538	snp	C/G	0.000159987	0.00894248	intron-variant	NEB, RIF1	GRCh38.p7	2:151525953	ACCGGTGGTTGATCA[C/G]TTACATCACTGACAT	4703
rs377008596	snp	A/G	8.81834e-05	0.00663957	missense	NEB	GRCh38.p7	2:151669065	CTTTGGCTTGAATAA[A/G]CTGAGGCAATTCAGG	4703
rs377015178	snp	C/T	8.28e-05	0.00643375	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151643878	CTGGTCGGGCAGGCA[C/T]GTCCACTGGTGCAGG	4703
rs377020291	snp	C/T			intron-variant, utr-variant-3-prime, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151497886	GGGATAGGGAATCTG[C/T]ACCCTCTAGAGAAGC	4703
rs377027708	snp	A/G	0.000165986	0.00910854	missense, intron-variant	NEB	GRCh38.p7	2:151618429	TCCAAGGAATCAATC[A/G]GAACCCAGCCAATGC	4703
rs377039628	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151577913	TTCTTTATTCACCAT[G/T]GTATCTTTAGTGCTT	4703
rs377045831	snp	C/T	0.000169986	0.00921759	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151514909	TTAATGGACTCTTCA[C/T]AATCTTTCCTATATT	4703
rs377047616	snp	A/G	0.000182601	0.0095534	intron-variant	NEB	GRCh38.p7	2:151697530	ACAGAAAGAGTGACA[A/G]TAGGATTGCTTACAT	4703
rs377054979	snp	A/G	6.62548e-05	0.00575526	missense	NEB	GRCh38.p7	2:151672596	TTGCCACATTCATAT[A/G]GTGGACCAGCTTGGG	4703
rs377073737	snp	A/G	0.00438332	0.0466095	intron-variant	NEB	GRCh38.p7	2:151707156	TAACTCTTAAAAGCA[A/G]CAGAGAAACTGCATA	4703
rs377076154	snp	C/T	3.38461e-05	0.00411362	missense	NEB	GRCh38.p7	2:151567209	TTGCCTGAATAACAT[C/T]GTTCTGGTCAGGATG	4703
rs377076974	in-del	-/AGTA	0.00318978	0.0398085	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151498446	GGAAGGGAGGAAGAG[-/AGTA]AGTAAGTTAGAGGAA	4703
rs377096416	snp	C/T	1.65853e-05	0.00287964	missense, intron-variant	NEB	GRCh38.p7	2:151640371	TCGCTCTGGAGGTCA[C/T]AGGCCTGCCGAGCAT	4703
rs377097560	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151678863	TGAGAACTTCGGGTG[G/T]GACAGGGGCATTTCA	4703
rs377103164	snp	C/T	0.00279162	0.0372561	intron-variant	NEB	GRCh38.p7	2:151577200	GCTTCCCATCGGTCA[C/T]AGGATAAACATCAAA	4703
rs377109601	snp	A/G	0.000169986	0.00921759	intron-variant	NEB	GRCh38.p7	2:151538003	AACACAAAGACAGCT[A/G]TAAGTCTTACCCAAA	4703
rs377109660	in-del	-/GTG			intron-variant	NEB	GRCh38.p7	2:151673787	GCCCAGGCTGGAGTG[-/GTG]CAGTGGCGCAATCTC	4703
rs377112785	snp	A/G	6.62844e-05	0.00575655	missense	NEB	GRCh38.p7	2:151554996	CGTCAACACTTCTTG[A/G]TAACGTATAAAGAGC	4703
rs377121323	in-del	-/GTTTT			intron-variant	NEB, RIF1	GRCh38.p7	2:151509394	TATTTTTATTGTTTT[-/GTTTT]TCTTTTATTTTTTCC	4703
rs377130044	snp	A/C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151656699	CATTTTATAGATGAA[A/C/T]AAGCTGAGACCCAGA	4703
rs377131345	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151636649	AGCTGGGTGTGGTGG[C/T]GCATGCCTGCAATCC	4703
rs377135465	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151614919	CAATCTGATGGAGCA[C/T]AACAATCTGATGGAA	4703
rs377137664	snp	C/T	1.66194e-05	0.00288261	missense	NEB	GRCh38.p7	2:151568410	TTCCAGTCTTTCCGG[C/T]ATTTAATCTAAAAAA	4703
rs377143618	snp	C/T	0.000370989	0.0136146	intron-variant	NEB	GRCh38.p7	2:151547551	AAAGAAAAAAAAATA[C/T]CCCAAAACATATGTA	4703
rs377146103	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151717939	GCTCACTGCAAGCTC[C/T]GCCTCCTGGGTTCAG	4703
rs377168325	snp	A/G	9.93937e-05	0.0070489	synonymous-codon	NEB	GRCh38.p7	2:151677769	GTCTTCCTTGTAGAC[A/G]TTCTACAGCAATGGA	4703
rs377168964	snp	A/G	0.000217856	0.0104346	synonymous-codon	NEB	GRCh38.p7	2:151665411	GAACTTCAGCTTCTC[A/G]GGGTGCTGGCGATAC	4703
rs377170982	snp	A/G	1.65814e-05	0.00287931	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151640634	ACCAATGTGGTGGCC[A/G]AGCTGCTTACGATAG	4703
rs377171458	snp	A/G	0.000167986	0.00916323	intron-variant	NEB, RIF1	GRCh38.p7	2:151490326	ATAGTAACCATCAAT[A/G]AGCTGGCCGGGTGGG	4703
rs377174386	snp	C/T	0.000431894	0.0146888	intron-variant	NEB	GRCh38.p7	2:151655781	GCTAGCCTTTCCTCA[C/T]GTGGGAGCTGTGTGG	4703
rs377179553	snp	A/G	0.000169986	0.00921759	missense	NEB	GRCh38.p7	2:151565090	TGGGAGATATGTGGT[A/G]TATCTGGTGAAAACG	4703
rs377180119	snp	C/G/T	3.31166e-05	0.00406908	missense, intron-variant	NEB	GRCh38.p7	2:151627618	TCTTGTAGTCCACAT[C/G/T]GCTGACTAAGGTCTG	4703
rs377182240	snp	A/G	1.65963e-05	0.0028806	stop-gained, intron-variant	NEB	GRCh38.p7	2:151612272	GCTGGTCTGCAGGCT[A/G]GCGATACTTCCTGTC	4703
rs377183242	snp	A/G	0.000168449	0.00917586	synonymous-codon	NEB	GRCh38.p7	2:151568624	TATACTTACATCATC[A/G]AGGATCTCGCCACTT	4703
rs377214303	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151491011	CTGGAGTATAAATCC[C/T]TTGAGGACTGTCTCT	4703
rs377226592	snp	A/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151524247	AATCTGGAAATCACT[A/T]CTTCCTGCAAGGTCT	4703
rs377228526	snp	C/T	9.9744e-05	0.00706131	intron-variant	NEB	GRCh38.p7	2:151725589	CAGATATTAGCCTAA[C/T]AAGACAGCAGTGAAA	4703
rs377231011	snp	A/C	7.03185e-05	0.00592911	intron-variant	NEB, RIF1	GRCh38.p7	2:151526289	GGAAAAGGGGCATTT[A/C]TTTAGCTCTGCTGGA	4703
rs377239300	snp	A/G/T	6.63405e-05	0.00575898	intron-variant	NEB	GRCh38.p7	2:151554917	GTCATTAAGGGGCGC[A/G/T]TGACCGTACTTACAT	4703
rs377243130	snp	C/T	8.67566e-05	0.00658565	synonymous-codon	NEB	GRCh38.p7	2:151545900	TACCTCACTCAGATG[C/T]GTCTTCAGTTCTTGC	4703
rs377244662	snp	C/T	1.66021e-05	0.0028811	missense	NEB	GRCh38.p7	2:151679988	GGCAGGTTGTATTTG[C/T]GAATAATTTCCTCTC	4703
rs377274148	in-del	-/CAAACAAA			intron-variant	NEB	GRCh38.p7	2:151628886	AAACAAACAAACAAA[-/CAAACAAA]AACAAAAGAAAAGAA	4703
rs377282917	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151726286	GGCAATATATTGACA[A/G]AAAATTCTATCCTTG	4703
rs377286332	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151673819	GCTCACTGCAAGCTC[C/T]GCCTCCCGGGTTCAC	4703
rs377295890	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151668795	ATGGGACACAACTTA[C/T]TTGACTGACTTTACA	4703
rs377301805	snp	C/T	0.000165986	0.00910854	intron-variant	NEB	GRCh38.p7	2:151675282	CCAGCAAAGACCCTA[C/T]TTACGTCACTTATAT	4703
rs377317466	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151622035	TTTGTTTTTTGAGAC[A/G]GTCTCACTCTGTCGC	4703
rs377336846	snp	C/G/T	4.96868e-05	0.00498411	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151492146	TTTGTTCCATTTCTA[C/G/T]CACTTTCCTCTGAAT	4703
rs377343559	snp	G/T	1.7257e-05	0.00293738	utr-variant-3-prime, intron-variant	NEB, RIF1	GRCh38.p7	2:151485753	CAAGTGTGATGCTTT[G/T]AAATGCCTAAATAGC	4703
rs377372435	snp	A/G	1.6593e-05	0.00288031	missense, intron-variant	NEB	GRCh38.p7	2:151650213	GTCTTTGCCAGAACT[A/G]TATCCATGGCATCAG	4703
rs377374622	snp	C/G/T	0.00495298	0.0495172	intron-variant	NEB	GRCh38.p7	2:151621071	TAGAATTCACATTCA[C/G/T]TCGAAAAGTATATTT	4703
rs377375638	snp	C/T	0.000135964	0.00824401	missense, intron-variant	NEB	GRCh38.p7	2:151636262	AGGCCTTGGCCGCCA[C/T]GATGGGGATGGCGTC	4703
rs377381673	snp	C/T	5.0043e-05	0.0050019	intron-variant	NEB	GRCh38.p7	2:151548266	ACAAAGCCATGGCTA[C/T]TGAAACTCAATATGT	4703
rs377385674	snp	A/C	0.000238199	0.0109107	intron-variant	NEB	GRCh38.p7	2:151565486	TGCACTTCAGCATGC[A/C]CAAAGCAAACTTACA	4703
rs377412501	in-del	-/A			intron-variant	NEB, RIF1	GRCh38.p7	2:151510680	TGTTGTTAATCTCTT[-/A]ACTGTGCTAATTTAC	4703
rs377428242	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151601589	ACCGGTAGTATACAC[A/G]CCACACTTTGAGTAA	4703
rs377429434	snp	C/T	4.97385e-05	0.00498666	missense	NEB	GRCh38.p7	2:151562124	CCTGACTCTGAAGGT[C/T]GTATGATTTCTTGGC	4703
rs377431945	in-del	-/AT	0.0209421	0.100162	intron-variant	NEB, RIF1	GRCh38.p7	2:151515071	TCACACATTTGAAAC[-/AT]GTATGATTGTACTTG	4703
rs377434935	snp	A/G/T	4.978e-05	0.00498878	intron-variant	NEB	GRCh38.p7	2:151563571	CAGCACACTTATGGG[A/G/T]CACAAATCCCGTGTT	4703
rs377443184	snp	C/T	6.71231e-05	0.00579284	missense	NEB	GRCh38.p7	2:151537918	TGGAAATGCTCTGGA[C/T]GATCAGGAATGGACC	4703
rs377452683	in-del	-/TGCTGGCTGTGCCAG	0.0119243	0.0762888	NEB	2	allele_origin=G(germline)/(germline)	2:151727802	CACCGGCTTTGCTGA[-/TGCTGGCTGTGCCAG]TGCTGGCTGTGCCAG	4703
rs377477857	snp	A/C/T			intron-variant	NEB	GRCh38.p7	2:151717842	ATCGACTTGACCATA[A/C/T]ACCTCCTTTGTTCTT	4703
rs377481097	snp	A/G	0.000182178	0.00954232	synonymous-codon	NEB	GRCh38.p7	2:151575725	AGCATTTGCTCTAGC[A/G]AGATTAATTTCTGGA	4703
rs377482159	snp	C/G/T	9.9431e-05	0.00705034	intron-variant	NEB	GRCh38.p7	2:151563601	TAAAGTGGACATTTA[C/G/T]TTACCGCACTCCTCA	4703
rs377487468	snp	C/T	8.33007e-05	0.00645317	missense	NEB	GRCh38.p7	2:151551782	CCCGGTCCAGATCCA[C/T]GGTTTTGGTAGTTGG	4703
rs377491119	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151515208	AGAGTGGAAGGATGG[A/G]TGCACCATCAGGACT	4703
rs377497238	snp	A/G/T	6.73991e-05	0.00580474	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151519047	GGTTTGTGAAGTTTC[A/G/T]TCAGGTCAGCCTTGT	4703
rs377528063	snp	A/G/T	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151690136	ACAGGGTCAGCAGGC[A/G/T]ATTGCATGAATGTGG	4703
rs377545263	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151629818	AAAAATACTATATAG[C/T]GTTAGAAATAAATGG	4703
rs377552363	snp	C/T	5.42667e-05	0.00520869	intron-variant	NEB, RIF1	GRCh38.p7	2:151494120	AAACTGCAAGAGTTA[C/T]TTTGCAAAATTAAAA	4703
rs377554789	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151575943	ATCTTTTCACGTAAG[C/T]TACTCAAATTTGATA	4703
rs377555125	snp	A/C/T	0.00024829	0.0111397	intron-variant	NEB	GRCh38.p7	2:151733081	TTGATTGTCACTACA[A/C/T]AAAATAGTTTGCTGT	4703
rs377567296	snp	A/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151526729	GTCACCTGGATCTAA[A/T]GGCCCTTGCACTGCT	4703
rs377570744	in-del	-/G			intron-variant	NEB	GRCh38.p7	2:151538346	TCTGGTTTTCCCATG[-/G]AATACATTTAGGAAA	4703
rs377576345	snp	C/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151729325	GGAGAATGGTGATAG[C/G]CACTGACATTATTCT	4703
rs377576558	in-del	-/AT			intron-variant	NEB, RIF1	GRCh38.p7	2:151505066	TACATACACACACAC[-/AT]GTTTTATATATATAC	4703
rs377582191	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151684461	AGAACTCACCAGGGC[C/G]TGGCACCATGCTAAG	4703
rs377592679	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151658593	CTATGATTAGGATGA[A/G]AAAGGAAATGAAATA	4703
rs377596701	snp	C/T	0.0111196	0.0737302	intron-variant	NEB	GRCh38.p7	2:151609512	CTGAATTAGATTCCA[C/T]TTTAATCCTGTGGCA	4703
rs377598058	snp	A/C	0.000167986	0.00916323	missense	NEB	GRCh38.p7	2:151706945	TCTGAAGCAGGAAGC[A/C]CATTATAATCTGCTT	4703
rs377599060	snp	C/T	5.75082e-05	0.00536198	missense	NEB	GRCh38.p7	2:151687628	AGGCCACACTCACAT[C/T]GCTGGTGTTCTTGGT	4703
rs377602828	snp	A/C	1.65605e-05	0.0028775	missense, intron-variant	NEB	GRCh38.p7	2:151643986	GCTGAACTTGGTCTT[A/C]CACTTCTCAAAGTCC	4703
rs377603856	snp	A/G	0.000133609	0.00817232	intron-variant	NEB	GRCh38.p7	2:151674608	AAAAGCAAACAGAAT[A/G]TCAGCATCTGTAAGT	4703
rs377606986	snp	A/C/G	0.000149093	0.00863284	missense, intron-variant	NEB	GRCh38.p7	2:151631288	TTGACCACATCCATA[A/C/G]ACCCAATGGGGACCC	4703
rs377617944	snp	A/G	1.905e-05	0.0030862	missense	NEB	GRCh38.p7	2:151695676	CATGTTTTGCTTTGT[A/G]ATTTAACTATGACAG	4703
rs377647449	snp	G/T	1.65616e-05	0.00287759	missense	NEB	GRCh38.p7	2:151697373	TTTGAGCTGTGACTT[G/T]CATGCAGTGTGAATG	4703
rs377649771	snp	A/G/T	0.000100472	0.00708717	missense	NEB	GRCh38.p7	2:151684932	ATATCAAGAGGTGCC[A/G/T]TGTAGATAGTTTTTG	4703
rs377652750	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151609285	GGGGTTGACGGGATA[A/G]GTGCACGAGATTGTA	4703
rs377653217	snp	C/G	0.000325947	0.012762	missense	NEB	GRCh38.p7	2:151672549	TTTGGTGTTCTCATA[C/G]TTCTTCTTGTATTCA	4703
rs377655799	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151532747	GAAAGCTCAATTAAC[C/T]TTTTTTTTTTGGTCT	4703
rs377656129	snp	C/T	5.04596e-05	0.00502267	missense	NEB	GRCh38.p7	2:151663568	TTTGAATCTGCATCA[C/T]ATTTTTGGCCAATTC	4703
rs377658340	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151528669	GTATAACCATTTAAT[A/G]TATTTTTAAGAAGTC	4703
rs377659398	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151549044	CATCAAGTCCCAGTT[A/G]AGTACTTGTGAAAAG	4703
rs377663194	in-del	-/GTG			intron-variant	NEB	GRCh38.p7	2:151657798	TATGAGGGTCACCAT[-/GTG]GTGGTTAGCTTGGTG	4703
rs377698227	snp	A/G	2.57935e-05	0.00359111	intron-variant	NEB	GRCh38.p7	2:151552802	GAAGAAAACAAGCCC[A/G]TGTTGGACCATTCCT	4703
rs377722150	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151651076	CAGGTACATGCCACC[C/T]CATCCAGCTTCAGTT	4703
rs377722971	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151632501	GCCAATATGGCGAAA[A/C]CCCATCTCCACTAAA	4703
rs377726497	snp	A/G	8.30268e-05	0.00644256	synonymous-codon	NEB	GRCh38.p7	2:151553398	ACAAGGCAAACTCAC[A/G]TCATCACGTAGATCA	4703
rs377734027	snp	A/G	0.000149116	0.00863342	missense, intron-variant	NEB	GRCh38.p7	2:151627153	ACATCCATAGACCCA[A/G]TGGGGACCCAGCCAA	4703
rs377735454	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151608704	TGTCAGACAAAAATA[C/G]CATTTCTGACCAACA	4703
rs377748897	snp	G/T	4.96874e-05	0.0049841	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151490016	AGATACCGTTGTCTG[G/T]TGGGTAGCAACTGAA	4703
rs377751674	snp	C/T	1.65737e-05	0.00287864	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151505478	GAGTATGGCCACTAC[C/T]GAGCTAATGTGCTTC	4703
rs377752982	snp	C/G	6.93265e-05	0.00588714	intron-variant	NEB, RIF1	GRCh38.p7	2:151525287	GTCTAAATAGAGCCA[C/G]AATTACTTTTATGAG	4703
rs377755862	snp	C/T			missense	NEB	GRCh38.p7	2:151549670	GTGTCCTTGATGTGT[C/T]TGAAGTGAGGAGTGT	4703
rs377765404	snp	A/C			intron-variant	NEB, RIF1	GRCh38.p7	2:151520039	CTTTCTAATGCAAAA[A/C]AAAAAAAAAAAAAAA	4703
rs386391505	in-del	-/AAA			intron-variant	NEB	GRCh38.p7	2:151719887	TGAGACCCTGTCTCA[-/AAA]AAAAAAAAAAAAAAA	4703
rs386418003	in-del	-/G			intron-variant	NEB	GRCh38.p7	2:151730616	GGCTCATTTCTTAGT[-/G]AAAAAAAAAAAAAAA	4703
rs386651673	in-del	ATG/CATATAATCTAT			intron-variant	NEB, RIF1	GRCh38.p7	2:151519878	TGTACATAGAGTGAT[ATG/CATATAATCTAT]TATCCAAACTGGGAC	4703
rs386651674	multinucleotide-polymorphism	CT/GC			intron-variant	NEB	GRCh38.p7	2:151561484	CTGCCAGAATGAATA[CT/GC]TTCTCTTGACTGAGA	4703
rs386651675	multinucleotide-polymorphism	AAG/TAA			intron-variant	NEB	GRCh38.p7	2:151607217	AAGTCCTGGATCAAT[AAG/TAA]AAAAACCTAAGATGA	4703
rs386651676	multinucleotide-polymorphism	AT/GC			intron-variant	NEB	GRCh38.p7	2:151609525	CATTTTAATCCTGTG[AT/GC]AATTGACCCAAGGAA	4703
rs386651677	multinucleotide-polymorphism	CT/TG			intron-variant	NEB	GRCh38.p7	2:151637165	CTGTGGAAGCAACTG[CT/TG]GAAAAGTCAAACCAC	4703
rs386651678	in-del	A/GTG			intron-variant	NEB	GRCh38.p7	2:151638823	TGTGTGTGTGTGTGT[A/GTG]TGTGTGTGTGTGTGG	4703
rs386651679	multinucleotide-polymorphism	AG/TT			intron-variant	NEB	GRCh38.p7	2:151675775	GAGAGAAAGTAGTAG[AG/TT]AGAATAAGTTTTTCA	4703
rs386651680	multinucleotide-polymorphism	ATA/TAG			intron-variant	NEB	GRCh38.p7	2:151722471	CTGAAGTATCTTCTG[ATA/TAG]GCAAGAGCTCTTTGT	4703
rs397689198	in-del	-/CAAAA	0	0	intron-variant	NEB	GRCh38.p7	2:151698099	CAAAACAAAACAAAA[-/CAAAA]AGAAAAAAACCTGAC	4703
rs397717850	in-del	-/AAG			intron-variant	NEB	GRCh38.p7	2:151628928	AAGAAGAAGAAGAAG[-/AAG]TCTGAATTTTCCACC	4703
rs397718862	in-del	-/GGC			intron-variant	NEB	GRCh38.p7	2:151717391	GTCTTCAAGGGAGGC[-/GGC]AATGTCCCAGCTCTA	4703
rs397722862	in-del	-/C			intron-variant	NEB	GRCh38.p7	2:151560800	TTCTCACACACTCCC[-/C]TACTAACTCCCAGGA	4703
rs397729869	in-del	-/AT			intron-variant	NEB, RIF1	GRCh38.p7	2:151494392	GATGGAAAGTAGTAT[-/AT]GTTTCCTAAGGAAGT	4703
rs397732305	in-del	-/A	0	0	intron-variant	NEB	GRCh38.p7	2:151656857	AGATGAAAAAAAAAA[-/A]GGCAAAAAAACAGAA	4703
rs397751859	in-del	-/ATT			intron-variant	NEB	GRCh38.p7	2:151550983	ATTATTATTATTATT[-/ATT]TGAAACGGAGTTTTG	4703
rs397772995	in-del	-/A			intron-variant	NEB	GRCh38.p7	2:151568432	CTAAAAAAAAAAAAA[-/A]TGAGAGGCAAGGGGG	4703
rs397775205	in-del	-/A	0	0	intron-variant	NEB	GRCh38.p7	2:151671997	AAGGAAAAAAAAAAA[-/A]CACCTTTCCCAAATT	4703
rs397868741	in-del	-/T			intron-variant	NEB	GRCh38.p7	2:151563032	TTTTTTTTTTTTTTT[-/T]GAGATGGTGTCCTAC	4703
rs397870075	in-del	-/A			intron-variant	NEB, RIF1	GRCh38.p7	2:151520054	CAAAAAAAAAAAAAA[-/A]TGGAAAAGGCTTCAG	4703
rs397870716	in-del	-/T			intron-variant	NEB	GRCh38.p7	2:151659680	AGTAAAAATGTTTTT[-/T]CCCCTTATCTTACAG	4703
rs397871464	in-del	-/A			intron-variant	NEB, RIF1	GRCh38.p7	2:151502400	CATAAAAAAAAAAAA[-/A]CTTAAAAGCTGCAAA	4703
rs397872591	in-del	-/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151491052	CTTTTTTTTTTTTTT[-/T]GAGATGGGGTCTCTG	4703
rs397976755	in-del	-/GGGT			intron-variant	NEB, RIF1	GRCh38.p7	2:151491062	TTTTTGAGATGGGGT[-/GGGT]CTCTGTTGCTCAGGC	4703
rs397986288	in-del	-/T	0	0	intron-variant	NEB	GRCh38.p7	2:151664032	CTTCATTTTTTTTTT[-/T]CCCGAGACTTGAGTC	4703
rs397986289	in-del	-/T	0	0	intron-variant	NEB	GRCh38.p7	2:151673751	TTTTTTTTTTTTTTT[-/T]GAGATGGAGTCTCCC	4703
rs398071409	in-del	-/AACA			intron-variant	NEB, RIF1	GRCh38.p7	2:151509332	GATGTAAGGAAAACA[-/AACA]GTTCTCATTGTCCTG	4703
rs398090759	in-del	-/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151531903	GTATTTGATCTAAAT[-/T]GTGGAAGAGAAGAAA	4703
rs398104845	in-del	-/A			intron-variant	NEB	GRCh38.p7	2:151540219	TTCTCTTTAAAAAAA[-/A]TGTGTGTTTTTTTCC	4703
rs398124167	snp	A/G/T	4.30024e-05	0.00463674	NEB	2	allele_origin=G(germline)/A(germline)	2:151706880	GATGCCCTAAGTGAC[A/G/T]TAAGTATATTTTTGT	4703
rs398124168	in-del	-/AG			intron-variant	NEB	GRCh38.p7	2:151694517	AACACCAGCGATGTG[-/AG]TGTGGCCTGGGGACC	4703
rs398124169	snp	A/G	9.67508e-05	0.00695457	NEB, RIF1	2	allele_origin=G(germline)/A(germline)	2:151494231	ACAAAGAAAATGTGG[A/G]GAAAGCCACCGCAAC	4703
rs398124170	snp	A/G			synonymous-codon	NEB	GRCh38.p7	2:151682662	AGACATCCTCAATGA[A/G]GTAAAGCCACTGGGT	4703
rs398124171	snp	A/C			missense	NEB	GRCh38.p7	2:151672650	GCTTATGAGAAGTCA[A/C]AGGGAAAGCATGTGG	4703
rs398124172	in-del	-/AAATAAACGAG			frameshift-variant, intron-variant	NEB	GRCh38.p7	2:151643269	TCTCGAGGATGAGAA[-/AAATAAACGAG]CCACCCAGATTTTGA	4703
rs398124173	snp	C/T			missense, intron-variant	NEB	GRCh38.p7	2:151642594	AAGGCAGCCAAGGCC[C/T]CCAGAGATATTGCAA	4703
rs527241220	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151713720	ATAGCTTCCCCACCT[A/G]GAAGGCCTGTTTCTA	4703
rs527248669	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151706114	GCTTTACAGTGATTT[C/T]CCAGCAGAGCTATTT	4703
rs527250558	snp	A/G	0.000313627	0.0125186	missense	NEB	GRCh38.p7	2:151549719	CAGTGGGCAGGGTGC[A/G]CAGGCTGGTTTTGTA	4703
rs527256438	snp	G/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151491608	GGAAGGAACTTCAGA[G/T]CCCAAATGAAAGTCA	4703
rs527281505	snp	A/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151492569	TTCCAGCAGATAGAG[A/T]TGGATAGGAGCTGGT	4703
rs527283653	snp	C/G	1.66087e-05	0.00288168	missense	NEB	GRCh38.p7	2:151663669	TCCTGAGACTTCTTG[C/G]CTGCCACCACACTGA	4703
rs527318565	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151621703	TCCATGGAAGTGTCA[C/T]TTGAGAACCACGCAT	4703
rs527322850	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151497915	GCAGGGACTTCAGCT[A/G]CTGAGGAAGGGCTGT	4703
rs527330600	snp	A/G	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151505414	CAGAAAGATGAGAGA[A/G]CACCAGGGTAGCAAT	4703
rs527347377	snp	A/G	0.00318978	0.0398085	intron-variant	NEB	GRCh38.p7	2:151676911	TACAGTGCCTGGCAC[A/G]TGGTAAATGTTCAAA	4703
rs527352987	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151620833	ACTGAAGGGAGTTAA[A/G]GTGGATGATGACCAA	4703
rs527378105	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151548822	CCTTTAGGTGTTAGA[C/T]TATTAAATCTGTGAC	4703
rs527398884	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151721228	CAATCTATCATATTG[C/T]TCATCAAAATTACTC	4703
rs527410677	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151556061	TAAAATCTTATCTAT[A/G]GTACTTTTCTTCCAA	4703
rs527412427	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151712893	CACAACAGAGTTGGA[A/G]AGAAAGGTTAGGGGG	4703
rs527449806	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151697980	CTGAGGCAGGAGAAT[G/T]GCTTGAACCCGGGAG	4703
rs527453526	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151691092	TACACAGTGACTCTT[C/T]AGTCAACTTGGTACT	4703
rs527480768	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151641743	ATTTTGGAAATAAAG[A/G]AAAAAATCTAGAGTT	4703
rs527492258	snp	C/G	0.000153858	0.00876957	missense	NEB	GRCh38.p7	2:151691873	ACTTACATCTTTACA[C/G]TGGTCCAGCTTCTTG	4703
rs527508632	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151577675	CCTCTGCCTCCTAGG[C/T]TCAAACGATTCTCCT	4703
rs527519394	snp	G/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151527205	CAGCCTAGCTGCCAG[G/T]ACCAAGCCCCTCCAT	4703
rs527528603	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151651528	TCTTGCATGTGCAGA[A/T]GGCTAAAAATAACTA	4703
rs527541818	snp	C/T	0.000798403	0.0199641	missense, intron-variant	NEB	GRCh38.p7	2:151606650	CGTGCTTGATTTCAA[C/T]GGCATCTGCCCTTAT	4703
rs527553539	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151657531	TGATATCAAGCCACC[A/G]ATAGTTTAACAACTG	4703
rs527576680	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151706536	AGATCTATCTTTGAA[A/G]GTCTCCTTCTGCTTC	4703
rs527577277	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151718513	CCACAATCAACCCCA[A/C]CTTACTCTCAGCTTC	4703
rs527580456	in-del	-/T			intron-variant	NEB	GRCh38.p7	2:151546558	TTTGGTTCATCTACT[-/T]TTTTTTTTTTTTTTT	4703
rs527598126	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151658101	AGTTTCTGTAAAGAG[A/G]GGCAAAGGGAAGAGT	4703
rs527598803	snp	C/T	5.02105e-05	0.00501026	missense	NEB	GRCh38.p7	2:151541469	TGAAGCTTCTGCCCT[C/T]GCTTGGCTCTTAAAA	4703
rs527610146	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151689905	AATTGGGTATGAGCT[A/G]ATTTGTGTCATTAAA	4703
rs527640575	in-del	-/A	0.00415799	0.045406	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151499415	CAAGAAAGCATCCAG[-/A]AAAAAACAAGAGCAG	4703
rs527672223	snp	A/G	1.65699e-05	0.00287831	missense	NEB	GRCh38.p7	2:151576245	ACAGGCGTCCGATAG[A/G]CACTGTCACAAAAGA	4703
rs527693892	snp	A/G	0.00358779	0.0422022	intron-variant	NEB	GRCh38.p7	2:151689738	ACCACATACAGCACT[A/G]TATTTCTCTGCAGCT	4703
rs527696498	in-del	-/CATCGGT			intron-variant	NEB	GRCh38.p7	2:151577191	CATCCTATGGCTTCC[-/CATCGGT]CATAGGATAAACATC	4703
rs527708642	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151601407	GAGCCACCATGCCTT[C/G]CCTGAAATAATTTTT	4703
rs527724374	in-del	-/T	0.0115144	0.0749975	intron-variant	NEB	GRCh38.p7	2:151637298	TTCAGTAGACTAAGG[-/T]TGGCATCAAGTGCAG	4703
rs527724982	snp	C/T	0.00119737	0.0244387	intron-variant	NEB, RIF1	GRCh38.p7	2:151531608	AGGCATAAGCCACCA[C/T]GCCCGGCCACAACAA	4703
rs527744844	snp	C/T	0.000399281	0.0141238	synonymous-codon, intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151496941	TTCTTGCCCAAGTAC[C/T]GAGCTAATATTTTCT	4703
rs527746468	snp	C/T	0.00118835	0.0243468	missense, intron-variant	NEB	GRCh38.p7	2:151594296	TGGCCCAGTTGCTTA[C/T]GGTAACCTTCTTTGT	4703
rs527760025	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151574364	AAATAATGATGATAT[C/T]AGGGGCACCCTCATT	4703
rs527760406	snp	A/G	1.72895e-05	0.00294015	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151531042	CAGCAACATGGGTGT[A/G]TCGTGGATTGTGGTG	4703
rs527778127	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151704732	CTCACGCACAGTGCG[A/C]GCACTCACTGACCTG	4703
rs527787338	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151648454	CTCTTTAAAAAATTT[C/T]TTTATTTCCATATAT	4703
rs527787405	snp	C/T	3.31417e-05	0.00407059	missense	NEB	GRCh38.p7	2:151656377	TCTTAGCCACTTGCA[C/T]GGAATGGACTAATTT	4703
rs527799915	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151538645	AAGTTCATTTGAGAG[A/G]AAAAAAAAACCCAAA	4703
rs527803367	snp	A/C	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151547801	GGGCATCTACTGACT[A/C]ATCAAGAATAAAATA	4703
rs527815508	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151705099	AAGTTATATAAGGTG[A/G]GAAATACGCAATCTC	4703
rs527821690	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151662972	TGTAGCCTTGCTTTC[A/G]TCTGCTTTGGGTTTG	4703
rs527832195	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151510939	AGAAGCAAGTTTGTG[A/G]AAACACAAGCACCAT	4703
rs527873088	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151684167	TTAATATACTTAACA[A/C]CACTGAACTGTACAC	4703
rs527896306	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151569702	GGATTTTAAAATCTT[A/G]GCAACTTAATTCAAA	4703
rs527904939	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151676353	TTCAGTCCAATTAAG[C/G]CTTCCTTGGATTTCG	4703
rs527929096	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151727551	AATTCAACAGTCACA[A/G]GAGCCTATAATTTGC	4703
rs527930624	snp	A/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151635894	CTAAGTTTATGAGTT[A/T]TATCTTCTATAAGCT	4703
rs527935329	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151628268	TGAGTCCACAGATAC[C/T]ATTTTATCCCTCCAT	4703
rs527940573	snp	C/T	0.00557542	0.0525036	intron-variant	NEB	GRCh38.p7	2:151723898	GGGGCACAAAATAAA[C/T]CTCTAATTAGAGTAA	4703
rs527959796	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151635080	ACTAGGAGTTTGATT[C/T]GAGGCAAGTTGCTTA	4703
rs527960458	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151649751	AGAATTATCCATTTA[A/T]CCTGATTCAGCTAAA	4703
rs527989906	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime	NEB	GRCh38.p7	2:151734427	ATAAATTTCCTCAGC[A/G]GCAAAGCCTCTCCCA	4703
rs527991803	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151681962	AATAATAACAATGTG[A/G]TGTGTATTATGCTGG	4703
rs528021136	snp	A/C	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151683422	ACCATAGGTGGTACC[A/C]AAAATTTACGTTTTA	4703
rs528030270	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151560788	TCTGTGTCTGTCCTT[C/T]TCACACACTCCCTAC	4703
rs528036824	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151576963	CTGTGTGGTAGTGCC[C/T]ATGTGCATTCTAAAA	4703
rs528089909	snp	C/T			intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151534597	ATGCCATTAACAACA[C/T]TAGGTTTTATGGCAT	4703
rs528112985	snp	G/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151529033	TCCCTATGCTCCTTT[G/T]TGAGGACCAATGCAG	4703
rs528116521	in-del	-/A	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151581692	AATAAATGGATGATG[-/A]AAAAAATTTTAAGTG	4703
rs528135373	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151609673	TTTTATATTAAACAA[C/T]GTGAATGGTACCCCC	4703
rs528140737	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151494507	TCAAAAGGATGAGAA[A/G]CCACCATCATTTTAC	4703
rs528145845	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151732298	TTAGATTTTATTTCT[A/G]GAATGTGAAGCTAAA	4703
rs528147715	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151644301	TATGAAATTCCATAC[A/G]TAATAAATGCATCCT	4703
rs528149253	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151578889	GAGTTCAAAACCAGC[A/C]TGGCCAAGATGGCAA	4703
rs528154006	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151536410	TATAATTATTATTTA[A/C]CTTTGAAAGTATTTT	4703
rs528160346	snp	A/C	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151652576	TTGGAGATGGAGAGA[A/C]GGTAGGATGCTGAGT	4703
rs528166825	snp	G/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151507626	ACTTCCGCATCTCTA[G/T]CCATAAAAATACACA	4703
rs528170584	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151535259	ACAACTATTCCTTTA[G/T]CGTAGCTCTTCTAAC	4703
rs528182275	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151653423	TTTGGGAGAGTGAAT[A/C]TATGAACTTTAGATT	4703
rs528188812	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151698868	TGGTCTCCATCTCTT[C/T]TTTTTTTTTTTTAAT	4703
rs528213899	snp	A/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151544380	GTGCGGTGGTTTTCA[A/T]CACAGGCTACATATT	4703
rs528223952	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151641635	GGTGCCTGACCTATA[C/T]ACATGATTTTTAATG	4703
rs528226745	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151702375	GCTCTGTAGATGTCA[A/G]TTAGGTCCGCTTGGT	4703
rs528258272	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151680885	ACTGAAGATTAATAC[A/G]TCAAAATCCTTGAAA	4703
rs528259973	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151558845	CTAAAACCATAAAAA[A/C]CCCAGAAGAAAACCT	4703
rs528289995	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151559589	AATATGGCATATATA[C/T]ACCATGGAATACTAT	4703
rs528297791	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151516164	ACTTTTCATTCATAA[A/G]GGAAAATCCAAATTA	4703
rs528334504	snp	G/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151515388	TTCCTAATCATGACC[G/T]GTTTTTTTAATATGG	4703
rs528353486	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151523763	TTCTCCATCAGCACC[C/T]TGTGCATACCCTGAT	4703
rs528372410	snp	G/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151517014	GACCTGGGGTCTAGA[G/T]TGAATGGATAACACA	4703
rs528373903	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151730747	CTCAATGGCCTGCAT[C/T]CTTTTCAGTGAAGTG	4703
rs528387620	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151638898	TTATATACTAAAAAT[C/G]TTAAATTTGGATCCT	4703
rs528399612	snp	C/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151731402	AGATGTCCAAGATCC[C/G]AAGGAGATATATTTT	4703
rs528428684	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151722039	TCAAAAGTTGGAGAC[A/G]CCATCAAATTGGTGT	4703
rs528428802	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151729962	GGAAATTTTTTTCTT[A/T]TGGTCCCCAAGATAG	4703
rs528433512	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151680366	GGATGGTTTTGATTA[C/T]ATATGATTTTTTTTT	4703
rs528434259	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151565321	GAATATAGATATCTA[A/C]AAGTGAATACAATTC	4703
rs528472700	snp	C/T	0.000399281	0.0141238	missense, nc-transcript-variant, intron-variant	NEB, RIF1	GRCh38.p7	2:151506931	AAATTCTTCTGATTT[C/T]CTTTTACACGCAGTA	4703
rs528473489	snp	A/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151522941	GTCAATCCGGAGACC[A/T]GCCTTTCACAGGAAG	4703
rs528496328	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151678924	ATATTTACACTGGTG[C/T]GATGTAAACCTAATT	4703
rs528519313	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151671627	GGGGAATCCAGGTCA[C/T]TATGGGTGCTGCTAA	4703
rs528519532	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151637807	CTTTCTGACAGGGGA[G/T]TAAGACTTGATGTTT	4703
rs528558526	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151521204	AGACACAAAATAACA[A/G]TGAAATCTGCCACAT	4703
rs528570189	snp	A/G	0.0023933	0.0345097	upstream-variant-2KB	NEB	GRCh38.p7	2:151736230	AAATAAAGCAAAACA[A/G]TGCGAAACAAAACAC	4703
rs528610168	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151571404	TTTTCTTGTGTTGGT[A/G]TATTGGTAACATTGA	4703
rs528614990	snp	A/C/G	6.6242e-05	0.00575476	synonymous-codon, missense, intron-variant	NEB	GRCh38.p7	2:151644037	CTGGATCTTGGCCAC[A/C/G]TGCATGGACCACATC	4703
rs528620935	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151551593	GAGGAAAGATAGATT[A/G]TGCTCTGTGTTTTTG	4703
rs528631745	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151685455	TTGAATGGATAGTCA[A/G]CTGGTTTTTTAACCT	4703
rs528660946	snp	A/G	0.000150218	0.00866524	intron-variant	NEB, RIF1	GRCh38.p7	2:151493891	TACAAAGTCATGCCC[A/G]AAAGTCACTACGAGG	4703
rs528722359	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151687013	ATTACTAAAGTCAAT[A/G]AAGAACGATACTCTA	4703
rs528727313	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151623858	AATGTGCTTCAATCA[C/T]CTCATGGCTTCAGGC	4703
rs528756686	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151499848	TGTAGAGATGGTCAA[A/G]TATAGAGGTTCAATA	4703
rs528787460	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151642473	ATAAACTGTTAGCAA[C/T]AGCTTTAACCTCATG	4703
rs528794843	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151652791	GATTTCAAAAGGTTC[A/G]AATTAATGGGTTCAC	4703
rs528809023	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151558706	CGATGGGGAGAAGAC[C/T]CCCTATTTAATGAAT	4703
rs528814044	snp	C/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151715703	CCTCCAGAACTGTGA[C/G]AAAATAAACGTCTAT	4703
rs528820555	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151550750	CTGAGGTAATCTTTT[C/T]ACCTCAACCTCCCAA	4703
rs528857504	snp	A/C	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151698788	GACTACAGGTGCCTG[A/C]CACCATGCCCGGCTA	4703
rs528861659	in-del	-/AAGTA	0.00199481	0.0315187	intron-variant	NEB, RIF1	GRCh38.p7	2:151509127	AGGAATTACATTTAT[-/AAGTA]AAGTATTGAAATTTG	4703
rs528876396	snp	C/T	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151578867	CGGGTGGATCACCTG[C/T]GGTCAGGAGTTCAAA	4703
rs528886615	snp	C/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151486107	GAAATACTTGCAAGT[C/T]ATGTATCTGATAGGC	4703
rs528895091	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151539788	TTTTAACCACTGTGT[C/T]ATGCATCATTCACAT	4703
rs528938852	snp	C/T	0.000766695	0.0195642	intron-variant	NEB	GRCh38.p7	2:151607465	AGCAGACAGATATTG[C/T]CCATAAAGGCTTTTA	4703
rs528950893	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151493173	TCTATTTTAGTGTAA[A/G]TTTTCAGTTGAATAA	4703
rs528960750	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151651718	TAATGAGTATACTAA[C/G]AGCATTTACTTGATG	4703
rs528962426	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151659178	AGAGATGCTAGGAAA[A/G]AAACAGTGTAAATTA	4703
rs528974814	snp	C/T	3.31466e-05	0.0040709	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151618317	TGCCAGCACCTGCTC[C/T]GGAGTGTCCGTTATA	4703
rs528975319	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151543406	TTTTTTCATGTTACT[A/G]TTGAAAGAGATAAAC	4703
rs528982427	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151533803	CCACCAAAATAGCTT[C/T]ATAGAAAAGAAGACA	4703
rs529015239	snp	C/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151486803	AATGTCTTAGGTAGC[C/G]AAATAATATAGTGAC	4703
rs529017806	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151542611	AAATGGTCATGAATC[C/T]TGGGCTCCTCACTTT	4703
rs529023851	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151615718	TATTTTTTTTGAAGA[C/T]GGAGTGTTCAATTTC	4703
rs529024553	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151698052	GCCCGGGCGACAATG[C/T]GAGACTCCGTCTCAA	4703
rs529047489	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151566087	AAGTGCTGTTAGATC[A/G]AGTGCTCAAATGCTA	4703
rs529053642	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151558970	TAAAGAACTTCTGCA[C/T]AGCAAAAGAAACTAC	4703
rs529067250	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151723033	TCATTCTGTTGTCAC[A/C]GAACAACTTCAACCA	4703
rs529100205	snp	C/G	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151522863	GCAAGACAGCAAAGT[C/G]AGAACAGGGAAAGCC	4703
rs529106025	snp	A/C	0.0146672	0.084371	intron-variant	NEB	GRCh38.p7	2:151554524	GTGATTGCACCACTG[A/C]CCTCCAGCCAGGGCA	4703
rs529135164	snp	C/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151514512	AAATAAAAAACAATT[C/G]CAATTTTTAAAGGGT	4703
rs529136096	snp	C/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151522045	GGAGCTAAGAGGCAA[C/T]TCTGCAATGCCATGT	4703
rs529137547	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151720103	GTTTAGTTAGAATTC[C/T]GTTGTTATGGAGAAT	4703
rs529166120	snp	A/G	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151529487	GAGATGCACCTTCCT[A/G]TCTCAGATCAGGGCA	4703
rs529171294	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151638196	GTCTTAGAGTTTAAG[C/T]TGGTCTCAAGTTCTG	4703
rs529175229	snp	A/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151528391	GGTTTTTTTCCCCTC[A/T]TTTTATTTTGAAAAA	4703
rs529190897	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151645777	AAAATTTCATTGAGT[A/G]TCTACTATGTGTCAG	4703
rs529199721	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151536623	AATATGCCCTAGAAT[C/G]AATCTGGCCCATAAC	4703
rs529200875	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151629075	TAAGATAATTTTCCA[A/G]AAAAAAATGAGTTGG	4703
rs529207958	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151645170	CAGGCAGAAGTAAAA[A/C]AATAGAGAAATGAAA	4703
rs529223188	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151692977	CCTGTCTCAAAAAAC[A/G]AAGAAGGAAAGAAAA	4703
rs529237074	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151686205	TGACACATACCAGTA[C/T]ATATAAAATGTTGTC	4703
rs529249679	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151572551	AAGTATATATATATA[C/T]ACTTTTTTTTTTTTG	4703
rs529254638	snp	A/G			synonymous-codon	NEB	GRCh38.p7	2:151656399	GACTAATTTGGGATC[A/G]TCCTCGAGACTGCGG	4703
rs529291298	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151728287	AAGCAAACTTGAGTT[C/T]GGGGAACAAAAGGTT	4703
rs529303347	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151577603	TGTTTGCCTTTGAGA[C/T]GGAGTCTCACTCTGC	4703
rs529307236	in-del	-/CAAA	0.00676609	0.0577691	intron-variant	NEB	GRCh38.p7	2:151538657	GAGAAAAAAAAAACC[-/CAAA]CAAACAACATTGTTG	4703
rs529315703	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151653619	ATCTATCAGCATCAG[C/T]TTGTTGAGGTTGATT	4703
rs529321293	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151677251	TTAAGCTTAAATTCT[A/G]TGTATGTATGTGTTT	4703
rs529322446	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151638881	AGTTCTTGCCTTTAA[C/T]CTTATATACTAAAAA	4703
rs529337570	snp	C/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151636769	CTGGGCAACAAGAGT[C/G]AAACTCCATCTCAAA	4703
rs529345289	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151566885	GCTGATACTTTTCTA[C/T]GTGAATGTGAGTGAG	4703
rs529351602	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	NEB	GRCh38.p7	2:151735254	AGCAAGAGCAGATAA[C/G]ATGGAAATCAGTAAC	4703
rs529354859	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151543442	GAAAACTTAATGCTT[C/T]TTCCAAGCTAAATTT	4703
rs529356194	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151689253	TCCATCACCCAGGCT[A/G]GAGTACAGTGACACA	4703
rs529359497	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151526467	CAATCAAAATGGATC[C/T]CGTGATGAATCTTTA	4703
rs529383426	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151650479	CATTTTAGATTTTCA[A/G]TAATAATTCCTAATT	4703
rs529387833	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151532729	AAAACAAGTTGCTAA[A/G]AGGAAAGCTCAATTA	4703
rs529389293	snp	G/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151527137	AAAGACTTGCTACCA[G/T]AATGAGGAGAAGAGC	4703
rs529425164	snp	A/G	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151499785	ATATTTAACAGGCCA[A/G]ATCTATGCAATATGG	4703
rs529427924	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151691065	CAGATTAACCTTACC[C/T]TGCTGAAGCCTTACA	4703
rs529431111	snp	C/T	0.00199481	0.0315187	intron-variant	NEB, RIF1	GRCh38.p7	2:151526564	AGCCCATTATTATTC[C/T]GTCTTTACAGAGGAG	4703
rs529481412	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151671562	TACTGTATTATGAAG[C/G]CTAATAAAATAGAAA	4703
rs529481846	snp	C/T	0.00438332	0.0466095	intron-variant	NEB	GRCh38.p7	2:151622987	ATGCCACTCAAGCTG[C/T]AGGGGCATTCTTGGG	4703
rs529482600	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151550656	TTTTATTTTATTTTT[A/G]AGACAGGGTCTCACT	4703
rs529497329	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151506058	AGGCACCTATTTTAG[C/T]AATATAAGCTGTTTC	4703
rs529504738	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151506706	AAAAATAAAAGTTAC[A/G]TTGTTAGCAGATTTA	4703
rs529518712	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151549912	AAGAGTCATAAAATG[A/T]GTCAGATTACTCTTC	4703
rs529518948	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151630253	GTCAGTAATCAATGT[G/T]GTTGATAGAGAACAC	4703
rs529524492	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151729032	AGAGAAACAGCTGCA[G/T]GCAGAAAATAAAGCA	4703
rs529531749	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151513509	AATAAATCAGATGAC[A/G]GAGGGACACTTTATG	4703
rs529536066	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151721354	CAAGGTCCTGCTGCC[A/G]GCATTCTCACAAGTG	4703
rs529541416	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151731692	TCTAGTTGAATCAAT[A/C]AAGTCTAGCACTAAG	4703
rs529554791	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151629727	TGACTTATATCCTAA[A/T]ATTTAAAAAAGGATA	4703
rs529570242	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151637306	GACTAAGGTGGCATC[A/C]AGTGCAGAGGAAATC	4703
rs529583359	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151624610	CATTTTTTAAGGCTA[C/T]ATTATTATAGGCAAA	4703
rs529604324	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151564164	TTTTATTTTATTTTT[A/G]TGTTTTTTGAGACAG	4703
rs529640937	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151635076	ACTCACTAGGAGTTT[G/T]ATTTGAGGCAAGTTG	4703
rs529661869	snp	C/G	3.56297e-05	0.00422061	intron-variant	NEB	GRCh38.p7	2:151568203	AGAGCCACCATAAAG[C/G]GTTAAAATGAGGAGT	4703
rs529664907	snp	A/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151567715	GATAAAAATAAAATT[A/T]AAAAAATAAAAATAG	4703
rs529679573	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151732931	AAACAGTGATATTTC[C/T]TGTCAATTCTAAATC	4703
rs529683537	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151725051	ACAGAGCATTACCCC[A/C]ATGACTCTAGGTCTG	4703
rs529685296	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151692767	TCAAGGCCAGGAGTT[C/T]AACACCAGCCTGGCC	4703
rs529704102	in-del	-/T			intron-variant	NEB	GRCh38.p7	2:151666518	TAGGTAACATCGAAG[-/T]TTTTTTTTTGTATTT	4703
rs529735446	snp	A/G	6.62372e-05	0.0057545	missense, intron-variant	NEB	GRCh38.p7	2:151640458	TCCACATCGCTGACT[A/G]AGGTCTGGCACTTCT	4703
rs529736855	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151682441	CAAGTTATACCTTAA[C/T]AAAATTGTTAAAAAT	4703
rs529738646	snp	C/T	6.79152e-05	0.00582692	intron-variant	NEB	GRCh38.p7	2:151674454	AGGCAAACACCTAAA[C/T]TTCACCTAAAATTTG	4703
rs529742011	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151732344	GGAAAAACCGTAAGA[C/T]GATAAAAACAAAAGG	4703
rs529784085	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151556117	ATCTTCCAAATAGAG[A/G]TGGGTCTGGGTAAAA	4703
rs529794859	snp	C/T	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151647361	GTGATCCACCTGCCT[C/T]GGCCTCCCAAAGTGC	4703
rs529799103	snp	C/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151524695	TTTTTGAGATGGAAT[C/T]TCACTCTGTTGCCCA	4703
rs529799872	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151557551	GATACCAAAGCCGGG[A/C]AGAGACACAACCAAA	4703
rs529801297	snp	A/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151516284	TACCTAGAGCATTTT[A/T]AAAAAATAACTGAAC	4703
rs529803903	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151711064	TTGAATTATTGCCCC[A/G]TCTGACTCCCAAATC	4703
rs529815073	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151639758	ACAGATAGATAGATG[C/G]CTTTTATTACTCAAT	4703
rs529834661	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151619827	CTGTTGTTCTTTCTG[G/T]GGTGGTGCTTTCTAT	4703
rs529838581	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151523876	CGGGCAGTTAATATA[C/T]GTATGTTTAATGAAA	4703
rs529844343	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151668523	TATGTTTTTAAATTA[A/G]GATTTATCAATATCC	4703
rs529856378	in-del	-/C	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151709586	TTTACTAATTATATA[-/C]AAGAGCCAAAGTTAT	4703
rs529869416	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151547305	TCTTACCTCCAACTT[A/G]TACTCTTTGTTTAGA	4703
rs529870670	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151619230	TAGGAAGATTTATAC[C/G]TGTTTAGAACTGATA	4703
rs529893589	in-del	-/A	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151696999	GGATGTCAACAAGGG[-/A]AAAATAGGATGTTTA	4703
rs529898558	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151503224	ATTTTGGTCAGGTAA[C/T]AATACACAACACACA	4703
rs529907435	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151627313	AAATTTCATGTATAC[A/G]TTCTTCAATATATGA	4703
rs529946520	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151626767	CTGACCTCATGATCC[A/G]CCTGCCTTGGCCTCC	4703
rs529959049	snp	A/C	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151509699	GTGACGTGATCTTGG[A/C]TCACTGCAACCTCTG	4703
rs529963270	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151718899	CTGTTTCCAACAATG[A/C]AGAACTATTCATAGA	4703
rs529974373	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151510457	TAGTGAGACCTGGCC[C/T]GCCATACTGGCATTA	4703
rs529978259	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151609127	CATTTAAAAAAATTT[A/T]TTTAAGGGATGGAGT	4703
rs529989952	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151544599	TCTGAGTGCGAGTGC[A/G]GGCTGAAATAACACA	4703
rs529991621	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151708794	CAACTTCTTCCATAG[C/T]CTTCCCTGTCTCAAT	4703
rs530007989	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151552824	ACCATTCCTTATGCT[A/T]GAAACTGCTGGTTTT	4703
rs530008835	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151546776	GTTGGCCAGGCTGGT[C/T]TCGAACTCCTGACCT	4703
rs530011001	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151634435	GATCATGAGGTCAGG[A/C]GATCAAGACCATCCT	4703
rs530026840	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151517509	TCTGAGAATCTTCAA[C/T]TATAGTCATGAATTG	4703
rs530032320	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151561566	ATCCCTGACAGCAGC[C/T]CCTCACTTTTTTTTT	4703
rs530092023	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151508478	CTGGATGAAGCTATG[C/T]AGCCAGACTGTTCAA	4703
rs530092700	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151713766	GTTCATCTATGTTAG[A/G]GCTACAAAATACAGC	4703
rs530094480	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151672850	CATATATTGGAGTTA[C/T]AAGTGAGTGTCACGA	4703
rs530095681	snp	G/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151502284	TGTATACTGCTTGGG[G/T]GATGGGTGCACCAAA	4703
rs530105295	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151609749	CTCAGAGGCACTGAC[C/T]GGGCAATGAACAAAT	4703
rs530125387	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151552395	ATAGAAATAAACTTG[A/C]TATGACACAGGGCAC	4703
rs530140578	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151659990	TCCTTGTGGTGGACA[C/T]GGAGATGTGCCACCA	4703
rs530148803	snp	A/T	0.00676609	0.0577691	intron-variant	NEB, RIF1	GRCh38.p7	2:151509051	GGGCTGAGGAATGAG[A/T]CTAGCCACTGTTATA	4703
rs530150106	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151724142	CACATGTCTCAAGGC[G/T]ACTCATAAAAAGATT	4703
rs530157211	snp	A/G	0.0023933	0.0345097	intron-variant	NEB, RIF1	GRCh38.p7	2:151501710	AGCTGCCAGGCTGCC[A/G]GCAGGAGTGGCTTGA	4703
rs530166491	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151559507	GTATGTTTATTGCAG[C/T]ACTCTTCACCATAGC	4703
rs530190152	snp	C/T	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151723298	TCTTATACAGAAGAG[C/T]TGCAGTGACCATCTG	4703
rs530213197	snp	C/T	0.206642	0.246211	intron-variant	NEB	GRCh38.p7	2:151584313	TAGGGAGAGGTCATA[C/T]GTGTGTGGTTTTGGA	4703
rs530215033	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151574032	ACGCTGGAGTACAGT[A/G]GCGTGATCTCGGCTT	4703
rs530237907	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151488466	AGCCTGGGCAACATA[A/G]TGAGCCTCTACCAAA	4703
rs530242068	snp	A/G	3.3123e-05	0.00406945	synonymous-codon	NEB	GRCh38.p7	2:151694371	CAGCATCTTGGGATC[A/G]TCATTAATGCTGAGG	4703
rs530250693	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151581683	ACATACTTGAATAAA[C/T]GGATGATGAAAAAAA	4703
rs530271998	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151537563	ATTGTTATGTGTCTT[A/C]ATTGCTTCATGAAGT	4703
rs530287109	snp	A/G	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151610317	TCTTCATTGGTGAAA[A/G]CATTCCCTGCAGCAA	4703
rs530297242	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151660357	CAAAACATATTCTTG[C/T]GTGTATGTATGTATG	4703
rs530308859	snp	A/T	0.0023933	0.0345097	intron-variant	NEB, RIF1	GRCh38.p7	2:151488953	TAATAGCTTTATAGT[A/T]TGTTTTGTTCTTTTT	4703
rs530317889	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151709328	CTTCCAGTGAGAAGA[C/T]ACTAAATCAAATTGA	4703
rs530320236	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151644703	AAATACTCAAATGTA[A/T]TTAGAAATTATGCCC	4703
rs530324617	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151536651	AACATCTTCTTAGAT[A/G]TTTTATTTACTATCT	4703
rs530329582	snp	A/G	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151530844	TCCAGTCAACTTACC[A/G]AATCATGAGCAAAAG	4703
rs530353267	snp	C/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151702926	TGATGTTAGCTTGCT[C/G]GTTAGTTGATGCAGT	4703
rs530360366	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151646811	TGTGCCACCATACCC[A/G]GCTAATTTTTGTATT	4703
rs530382185	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151487667	AATGAGCATCCTACC[A/G]TTTATCTTTGGGCAA	4703
rs530458106	snp	C/T			intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151506751	GGTCTCTGGAGATGA[C/T]TTTGGAGCAAAGTAT	4703
rs530468906	snp	A/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151523807	AACAAAATTTTAATG[A/T]TTTATCCATGGACAA	4703
rs530477924	snp	A/C	0.00011372	0.00753971	intron-variant	NEB	GRCh38.p7	2:151581634	ATTAGTAAATAAGTC[A/C]ATTACCACATAAATA	4703
rs530488571	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151672057	GCATTTTGTATCTAT[A/C]ACCATTGCAGCCAAC	4703
rs530489622	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151637571	TGGAATAGGGGGTTG[C/T]GGGCAAAATGGGGAA	4703
rs530496513	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151687585	GGAAATGTCCCCAAG[G/T]CCACCCTGTCCAGGT	4703
rs530498417	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151653882	GTAGGAGAAAATGAA[A/G]GAAGCATTATATTTT	4703
rs530505669	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151560057	CTTCTACTATATTTA[A/T]ACAGCTCATGAGATT	4703
rs530546903	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151557907	ACAAACCCACAGCCA[A/G]TATCATACTGAATGG	4703
rs530561318	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151693761	TATATTCCTTTGGGT[A/G]TATGCCCAGTAATGG	4703
rs530565802	snp	A/T			missense, intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151534240	TGGTCGCCTGCGGTC[A/T]TAGCCAGCAGATGTC	4703
rs530569239	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151731501	CCTGGCCATTTTTTC[A/G]AATGCACCACCCTCT	4703
rs530601099	snp	G/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151503119	ACGCTGAGGAATCTT[G/T]TTAATTCTACTTATA	4703
rs530604506	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151645999	AAAAGCCACTAAATA[A/C]GGAATCTAAGTCATA	4703
rs530610541	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151523071	TTTCAACATCATAGT[C/T]GTTTGTTTTTAAATT	4703
rs530643847	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151667707	TAATTTTTTTTTTTA[C/T]TTCTGTAGAGACAGG	4703
rs530658048	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151626681	AGCTGGGACTACAGG[C/T]GTCTGCCACCATGCC	4703
rs530661756	snp	G/T	0.00159617	0.0282053	intron-variant	NEB, RIF1	GRCh38.p7	2:151488379	TGGCCGGGCTGAGTG[G/T]CTGATGCCTGTAATC	4703
rs530690335	in-del	-/G	0.00318978	0.0398085	intron-variant	NEB	GRCh38.p7	2:151689977	TCTTGAGAAGGATGT[-/G]ACTACTCTCTAGGAC	4703
rs530692325	snp	C/G/T	0.000116562	0.00763338	missense, intron-variant	NEB	GRCh38.p7	2:151633679	AGGTCATAGGCCTGC[C/G/T]GAGCATGGATGACAT	4703
rs530695897	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151615146	AAGATTCCAGAATAA[C/T]GCATTATGGTCCATT	4703
rs530698691	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151732323	GCTAAAGGCAAGAGC[C/T]GGTGAGGAAAAACCG	4703
rs530701650	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151566167	AGGCTTACCAAGGAG[G/T]TTGTACTTTTAGATG	4703
rs530721101	snp	C/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151516234	CTAATTTTACAGAAA[C/T]GGCTGTTGAAATAAG	4703
rs530734065	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151553158	AAATAGCCTAAAACA[C/T]AGAAAGAGAAGATGC	4703
rs530736055	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151560845	GGGGCTTATTTAATT[A/G]TACCTACTAGAATTT	4703
rs530755893	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151611947	ACTGCTCAGAAGGGT[A/G]AGTGCATCACTCCAG	4703
rs530774035	snp	A/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151723237	AATGAGACATCATAA[A/T]TTATAACAATTCTAG	4703
rs530781574	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151681782	TTATGAGCCTCAAGA[A/T]CATCACTATTTTTTC	4703
rs530783400	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151673794	GCTGGAGTGCAGTGG[A/C]GCAATCTCGGCTCAC	4703
rs530788800	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151559432	TTGACCCAGCAATCC[C/T]ATTACTGGGTATATA	4703
rs530840484	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151672760	TCACATATAAAGACA[C/T]TCAGAGCTTTGTGAC	4703
rs530873244	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151560468	GAATTATTTCCTGGA[C/T]ATGCCCACGGGAGTG	4703
rs530910991	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151508451	CCTCCAGTGGCAGTA[A/G]TCCTCGCTGGGCTGG	4703
rs530914597	snp	C/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151521852	AATCTGAGTTCAGCA[C/T]TTTTGGCCTTCCTTT	4703
rs530915015	in-del	-/TTCTA	0.0023933	0.0345097	intron-variant	NEB, RIF1	GRCh38.p7	2:151510648	ATATTGTTATAATTG[-/TTCTA]TTTTATTAGTTATTG	4703
rs530959473	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151565370	TTAAGACATACCCCC[A/C]AAAGATGATCTTAGA	4703
rs530973409	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151624071	CAATGAAGGAACCAC[A/G]GGCAATGGGTTGAGA	4703
rs530974339	in-del	-/G	0.00159617	0.0282053	intron-variant	NEB, RIF1	GRCh38.p7	2:151519889	GATCATATAATCTAT[-/G]TATCCAAACTGGGAC	4703
rs530981229	snp	C/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151515518	ACACTGAGTTTTGAC[C/G]TGTTTTTTAAAAATC	4703
rs530990385	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151679123	GACTCCACAGAAATC[A/T]TGGGGAGGGGGATTC	4703
rs531002685	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151610268	AAAGCAATGTTTTAT[A/G]CTGTTTTAAAAATAA	4703
rs531006251	snp	A/C	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151487595	ATAATATCACGAATT[A/C]TTCAGCCATTTTCAT	4703
rs531018317	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151494532	TTTTACCGCTAGTCT[C/T]TCAATGTCAAGCCCC	4703
rs531022313	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151702883	TTTAAAGTTAATATT[A/G]TTATGTGTGAATTTG	4703
rs531041156	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151609684	ACAATGTGAATGGTA[C/T]CCCCAGCCCCACCCC	4703
rs531048848	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151694828	GGGCTTCTCTACTCC[A/C]CATGAGAATTTTTTA	4703
rs531075623	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151617238	ATCAAGTGAGAACTA[C/T]CTCTTCTACTGAAAA	4703
rs531081657	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151648722	TAAAAACCAAAAATA[C/T]TTCTAGATGTTGCTA	4703
rs531085311	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151535462	TGCAGAGGTGCTGAT[A/G]TTTGCGGGGCTCTCC	4703
rs531108520	snp	C/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151544534	TCTCATACTGAGCCA[C/G]AGTGGAAAAGCACAA	4703
rs531112299	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151625214	GCACAAATTTTGAAG[C/T]AAGTACTAATTTGAT	4703
rs531138961	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151652225	CTCCAAAATTCCTTT[A/G]AAGAATTTTTTTATT	4703
rs531169443	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151660276	CTTCCCAAAGACTAG[A/G]ATCCCTAAAAAATAC	4703
rs531172776	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151653446	TTTAGATTGGATTTT[C/G]AGAAAGAAGAGTTAA	4703
rs531195692	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151676249	ACCTCTAAGTCCTCA[C/T]TGCCTTTAAGAACAA	4703
rs531200956	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151669211	AGACTCCTTTAAAAC[A/G]GAAGGCTATCATTTG	4703
rs531201942	snp	A/G	0.00199481	0.0315187	intron-variant	NEB, RIF1	GRCh38.p7	2:151501526	CAACCTGGACCCATC[A/G]TTTTTTAGGTAGACT	4703
rs531215710	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151555134	TTAATGGGAAAAACC[C/T]GACTCTGAGATCCAC	4703
rs531234795	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151659912	ATTAATTTAATCAGT[C/T]CTCTGGTGATGAATA	4703
rs531237676	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151658858	AAAATCCAATCACAC[A/C]GTTCAAATTCTTAAC	4703
rs531240193	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151616660	AATTGTGCCACTGCA[C/T]TCCAGCCTGGGTGAC	4703
rs531257691	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151732552	GTGGCTCCAACAATC[A/G]CTGTGACCTTCATGC	4703
rs531314016	in-del	-/AGA	0.00676609	0.0577691	intron-variant	NEB, RIF1	GRCh38.p7	2:151501256	GGAGATCTGGAAAAC[-/AGA]AGAAGGATTCAGTTG	4703
rs531315555	snp	G/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151510751	CAGTATATATAGGGT[G/T]AGGTATTGTCTGTAA	4703
rs531322067	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151719694	GACCAGCCAGGGCAA[C/T]ACGGTGAAACCCTGT	4703
rs531334594	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151620730	AAGGAGTCAAATGAG[C/G]CACATTCCAGTCTAG	4703
rs531377534	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151706481	CTTAGGGGCCCATCT[C/T]TTAAGTTCTGTTGTT	4703
rs531385680	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151577114	CTAGTAAGTTCTCTA[C/T]ACAGCAGCCAGAATG	4703
rs531386439	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151676464	TTAAAACACAAGCCT[A/G]ATAATGCGGCTCCAT	4703
rs531417831	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151690584	AATCTAGCAGCCTCA[G/T]TTGTGTTTTATTAAA	4703
rs531424377	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151605616	TTGAACAAAGAGAGA[C/G]AAAACTGGGAATCAA	4703
rs531442897	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151518601	AAGTTCAGTATTGTC[C/T]GTTAAGATGTAAACA	4703
rs531445719	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151634997	GAGAAAGTGTAGGTG[A/T]GTCAGCAAGAGACAA	4703
rs531447001	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151543635	CCCAAGCAATTTTTT[C/T]CTTATTTTTAAATTT	4703
rs531447914	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151650031	AGGATAGTTGCTAAT[G/T]CAAATAAAATGATCC	4703
rs531451107	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151727442	AAATACCAATAAATG[C/T]TTTATGATTGGCCTT	4703
rs531451526	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151645556	TTATTTAAAGTGCCT[A/G]TTGATCTTGGACTTG	4703
rs531466579	in-del	-/TA	0.0248432	0.108648	intron-variant	NEB	GRCh38.p7	2:151561610	ACACTTTTTTTTTTT[-/TA]TTATTATACTTTAAG	4703
rs531472572	snp	A/C	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151490757	TACAGCCAGGTTTCA[A/C]ATCCAAGAGTCTATT	4703
rs531491352	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151712768	GACCCTCTCTACCAG[C/T]GAAGGGGTCCCACTC	4703
rs531536677	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151659407	GCTCAAACAATCCAT[C/T]CTCCCACCTCAGCCT	4703
rs531537640	snp	A/C	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151491523	CTTATCTAGAAAGTA[A/C]GTTTTGCTCACTAGT	4703
rs531538100	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151631673	ACAGAAACCACACCC[A/G]TGCCCAACATCAGGC	4703
rs531545323	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151518059	GGAGTTACCATGAGG[A/G]GTTTGTCCCCTCATA	4703
rs531576697	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151657400	TTGAGTTTCATATAG[A/G]TGGCATGTCATGACA	4703
rs531581372	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151704726	CTTCGGCTCACGCAC[A/G]GTGCGAGCACTCACT	4703
rs531604132	snp	C/T			missense, intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151498294	TTGTGTTTGACTCTC[C/T]GCATCTCAGGAGTGA	4703
rs531611570	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151492986	TTCAGAGTATTACCC[A/G]TGTCATAAAGTATCT	4703
rs531618541	snp	A/T	0.000101042	0.00710711	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151526971	TGTTTTTGTCATCAG[A/T]GACAGAAAGCTTGCA	4703
rs531628640	snp	A/G/T	3.40514e-05	0.00412611	intron-variant	NEB	GRCh38.p7	2:151540653	GGTTTTAACAAAGTA[A/G/T]TTTTCTTTTTACCCA	4703
rs531658423	snp	A/G	0.00279162	0.0372561	intron-variant	NEB	GRCh38.p7	2:151661378	CAGGGGGTTTGCTCC[A/G]TGGCTTAGCATAATA	4703
rs531663279	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151697120	CTATGGAAGGCAGTC[A/G]CATTCAAAGTTCAGA	4703
rs531664908	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151548690	GCCAGAGAAAAATCT[C/T]TATTTTTAGCCCCAG	4703
rs531666957	snp	C/T			missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151501422	TGATTGAGTTTGACT[C/T]GCTCCATCTCAGGAG	4703
rs531673549	snp	A/C			intron-variant	NEB, RIF1	GRCh38.p7	2:151495029	CTGTAGGCCCTCAGA[A/C]AAAGCAAAGGGTTTC	4703
rs531681895	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151495617	AGAGCACAAGCTTAC[A/G]GGAAATGGTTTACTA	4703
rs531692437	snp	A/G/T	3.31489e-05	0.00407107	missense	NEB	GRCh38.p7	2:151662277	TTTTTCTCTGCTTCC[A/G/T]GGGAGCCCAGAGGGA	4703
rs531693249	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151538347	TCTGGTTTTCCCATG[A/T]ATACATTTAGGAAAA	4703
rs531694264	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151654721	CAATGTCATAGGCAC[C/T]TTTATGGTCCCAATT	4703
rs531711771	snp	A/G	1.88692e-05	0.00307152	synonymous-codon	NEB	GRCh38.p7	2:151537872	GATGTCAACACTCAC[A/G]TCACTGACTGTGTCA	4703
rs531715678	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151618577	AAAAATACCGATGAA[C/T]AGTTAAGGTTCCTAG	4703
rs531723796	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151701272	TTCGTTTTGCCAGTA[G/T]TTTATTGAGGATTTT	4703
rs531729514	snp	C/T	0.0107246	0.0724382	intron-variant	NEB	GRCh38.p7	2:151593635	CTGTATCTATATCCA[C/T]CCTGCCCCCCATCTC	4703
rs531732495	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151669662	TGGGTAGACGTGGGG[G/T]TGGAGCAGTATTAGA	4703
rs531748728	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151546647	GACTGCAACCTCCGC[C/T]TCCCGAGTTCAAGCG	4703
rs531768093	snp	A/G	0.000696829	0.0186529	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151591396	CTGGATCCCAATGGC[A/G]TCTGCTCGCAGGTCA	4703
rs531768201	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151611858	AGATGGCTAAAGACA[C/T]GTAAGTGGCCTGAAT	4703
rs531770073	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151726107	GTGCATAATTTATCA[C/T]TATAAATGTTTTGGG	4703
rs531781478	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151545670	GCCAGTATGAATATG[C/T]GTATCTTACCAAAAG	4703
rs531818635	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151581257	TATCTATAAGTTTTA[C/T]GTTGTGTTTTTGGAG	4703
rs531825244	in-del	-/ATC	0.0023933	0.0345097	intron-variant	NEB, RIF1	GRCh38.p7	2:151495151	GGCTCTTATATCACT[-/ATC]ATCATGGCGAATCAG	4703
rs531829566	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151718728	ACAACCCCAAACTCT[C/T]CTTCTTCATTAGCTC	4703
rs531833307	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151547178	ATTCCATGTTGAATG[C/T]AGAATGGTGGTCACT	4703
rs531840938	snp	C/T	1.65976e-05	0.00288072	missense	NEB	GRCh38.p7	2:151710436	CTTCCCACTTAACTG[C/T]GCTAATGTTATCAGC	4703
rs531867067	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151575606	CGGGAAGTCAGGGAC[C/T]GAGTCCATCTTCCCT	4703
rs531869863	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151704560	CAGGATATAATCTCG[C/T]GGTGCGCCGTTTTTT	4703
rs531888998	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151648280	TGAGATGTGTGTGTC[C/T]GGCACTTTTCTTTTT	4703
rs531895099	snp	C/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151507702	ATAAATTGTGTGTCT[C/G]TCTTGTTAATCTGTC	4703
rs531900016	in-del	-/C			intron-variant	NEB, RIF1	GRCh38.p7	2:151530782	CCTGGCTTGACTGAG[-/C]CCCAGGTGTCTGCCA	4703
rs531902900	snp	A/G	2.83998e-05	0.00376817	intron-variant	NEB, RIF1	GRCh38.p7	2:151530950	TACATCTCATTAGAA[A/G]GAGGCCAAGATGAGA	4703
rs531906107	snp	G/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151503334	TAGTTTCTTATATGA[G/T]ATATTTGTAAATACC	4703
rs531914447	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151569057	CCATTTATACAATGC[C/T]AAGCATCAGTGAGTG	4703
rs531920220	snp	C/G	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151688990	TGAAATTATGGAAAG[C/G]AAAACCGTGGATAAG	4703
rs531944752	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151562054	ATCAGCCCACTGACA[A/C]CACCATGGATTCTGA	4703
rs531949723	snp	C/G/T	4.97305e-05	0.0049863	synonymous-codon	NEB	GRCh38.p7	2:151576235	AAGGTTCACCACAGG[C/G/T]GTCCGATAGACACTG	4703
rs531975357	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151704836	TGCGTCGCTCGCTCA[C/T]GCTGGGAGCTGTAGA	4703
rs531980706	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151641914	GGTGTGCTGCACCCA[C/T]TAACTGATCATTTAC	4703
rs531981196	in-del	-/AT	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151553652	GGGAGCCACAGAAAC[-/AT]GTGTACACAGAGCCC	4703
rs531989234	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151634515	GGCGTGGTGGCGGGC[A/G]CCTGTAGTCCCAGCT	4703
rs531996429	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151675100	GAAGAATGTTATGTC[C/T]TTTAAAATTGTCCTA	4703
rs531998257	snp	A/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151503957	GCTTAATCAGTTTAT[A/T]TTTCAGGAAGAGCAT	4703
rs532040825	snp	C/T	5.86161e-05	0.00541337	intron-variant	NEB	GRCh38.p7	2:151697696	TTCCTGTCACTCCCA[C/T]GCTGATTATAACACT	4703
rs532076837	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151524136	AGAAAGGTCTAGACA[A/G]CTTAGAGGGAAACGA	4703
rs532095196	snp	C/G	0.00358779	0.0422022	intron-variant	NEB	GRCh38.p7	2:151733008	CTTTAAATGATGACT[C/G]TTTGTGAAGTTATAA	4703
rs532130242	snp	A/G	0.000415901	0.0144145	missense	NEB	GRCh38.p7	2:151679728	GGACTTACGTCACTC[A/G]CCGCCTGCCTGGCAG	4703
rs532139457	snp	C/T	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151716283	AGCTGAGATTACAGG[C/T]GCCCGCCACCACGCC	4703
rs532154971	snp	A/T	0.00318978	0.0398085	intron-variant	NEB	GRCh38.p7	2:151675524	ATTTTCCTATTTTTT[A/T]AAATAAAACAAGCAT	4703
rs532164483	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151613599	CTATTATAGTTTGAT[A/G]TAGTTTGGCTCTGCA	4703
rs532173583	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151510519	AGGTTTCACTTTCCA[C/T]GGTTTCAGTTAACTG	4703
rs532178479	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151705157	CTTATTATACAAACA[A/G]TTAGCCTTCAAAATT	4703
rs532209748	snp	A/G	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151517671	GTTGCTCCTAGGCTA[A/G]AAACCTGTACAGCAT	4703
rs532239472	snp	A/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151525542	AAAATATATGGAACC[A/T]TATGGGACTCATATA	4703
rs532241403	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151619928	TCATTGGCACATGTC[C/T]ACAGAATAACCCCAC	4703
rs532244536	snp	A/C	1.75523e-05	0.00296241	intron-variant	NEB	GRCh38.p7	2:151656489	AAATATGAGTTTTTA[A/C]ACAGAGCAATTCCTT	4703
rs532258293	snp	C/T	0.000798403	0.0199641	utr-variant-5-prime	NEB	GRCh38.p7	2:151733735	AATGGGGTTATTTTC[C/T]TCCCGAACACCATTG	4703
rs532276976	snp	A/G			intron-variant, utr-variant-3-prime, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151497802	ATGAGGAAAAAACAC[A/G]GTCATCCAAGGAGCC	4703
rs532278571	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151496513	ACAAAATGCCACCAG[C/T]TACTTTAGTGGAAGC	4703
rs532292844	in-del	-/GAG	0.0225045	0.103662	intron-variant	NEB, RIF1	GRCh38.p7	2:151500444	ATAATTTGTGTGTTA[-/GAG]GAGTTTTTCAGCAAC	4703
rs532323749	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151546505	TCAGGAAACACAAAA[A/G]ATGGAGTAGCAACAC	4703
rs532330829	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151547344	TCAGAAAAGGCTGTT[C/T]AAAGACCACTGGTTG	4703
rs532343989	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151705829	CTCAGGAATGAAAAA[C/T]CAAATATCATATGCT	4703
rs532344337	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151663174	GGTTGGGAGGGAGGG[G/T]CTGGAGCTATCAGGT	4703
rs532345972	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151497120	AGGTCAGCTTCCTTG[C/T]TAAGACAAAACACAG	4703
rs532351026	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151696234	TGTACTGAATACCTG[C/T]TGTTGGCCAGGGTAT	4703
rs532370784	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151667677	GAACTACAGGTACAC[A/G]CCACCACATCTGGCT	4703
rs532406299	snp	C/T	0.00318978	0.0398085	intron-variant	NEB	GRCh38.p7	2:151634448	GGAGATCAAGACCAT[C/T]CTGGCTAATATGGTG	4703
rs532408242	snp	G/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151504604	AAGAAAATCAAATGA[G/T]AGTTCAGTCCTCCAT	4703
rs532427194	snp	A/G	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151674281	TGTCAGATTTATGAC[A/G]GCTCTACCAAGTGGG	4703
rs532431337	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151667037	AATATAACTTAATTT[A/G]TAAAAAAAAAAATTA	4703
rs532438756	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151661183	TACGTGCTAGTTCTA[C/T]GATTCTCCTCTTGGC	4703
rs532462595	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151555112	TATTATTAAAACAGC[A/G]TAAGACTTAATGGGA	4703
rs532535946	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151495487	CTGTACTCAAGTACT[A/G]GAGAAACCTACAGAT	4703
rs532539798	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151611104	AGCAATATAATGGTT[G/T]CTATTAGTAATTCTT	4703
rs532547534	snp	A/G	0.000133638	0.00817321	synonymous-codon	NEB	GRCh38.p7	2:151688325	ATTGACTCTGTGTTG[A/G]ATAAACTGTGGAGCA	4703
rs532618407	snp	C/T	0	0	intron-variant	NEB	GRCh38.p7	2:151618058	AGAACAAAACTTAGT[C/T]TCAAAAAACAAAACA	4703
rs532629827	snp	C/T	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151553659	ACAGAAACATGTGTA[C/T]ACAGAGCCCTGCTTC	4703
rs532647648	snp	C/T	9.1245e-05	0.00675383	intron-variant	NEB	GRCh38.p7	2:151591324	AGTTAGTGTTTGTTC[C/T]GGTTGGGAAGGAGGA	4703
rs532675271	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151542629	GGCTCCTCACTTTGT[A/G]ATATTCCTGAAATCT	4703
rs532687013	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151718058	CGGGGTTTCACCATG[A/C]TAGCCAGGCTGGGCT	4703
rs532710372	snp	A/G	0.000399281	0.0141238	synonymous-codon	NEB	GRCh38.p7	2:151694419	TTTGTTTTTTTCATA[A/G]TCTTTCTTGTACATC	4703
rs532715542	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151575442	TCTTTCACCTTCTTT[A/G]TCCCCTTATTCAAAA	4703
rs532726419	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151533080	TAGATGAAAACATTA[A/G]ATATTCAGACCTTTT	4703
rs532755200	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151592157	GGAAAAATGAAAAAC[A/G]ATGGAATGGTCAATT	4703
rs532783102	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151530896	ACTAAGTTTTAGGGT[A/G]GTTGTTACACAGGAA	4703
rs532789868	snp	A/C	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151492973	AGAAGGCATCCATTT[A/C]AGAGTATTACCCATG	4703
rs532797761	snp	A/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151499681	CCTAAGACCACTAAA[A/T]TACTCAGTGTACAAT	4703
rs532800289	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151658193	TTTTTTTTGTTTTTG[A/G]GCAGAATGCTTCGTT	4703
rs532800993	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151648208	TTATTTCAATAAAAA[A/T]TTTTTTTGTCTCATT	4703
rs532815235	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151711364	GCTCATAAAAATGTG[C/T]TAACAGACATAACTA	4703
rs532820519	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151527612	AGGAGAGAAAGGAAT[C/T]ACTTGATTCAGTAGG	4703
rs532828308	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151664284	GAATAGACTCTAAAG[C/G]CTACTTATTTTAACA	4703
rs532852115	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151622764	CAGTATTATTGTCTA[G/T]TATTATTCTCTTTTA	4703
rs532854253	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151671497	TTTGACAATAAATTG[C/G]TACTTTCTATAATGG	4703
rs532865070	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151657663	GAAGCAGGAGGCAAG[A/T]ACAACACAAGACTTT	4703
rs532884424	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151501652	CCTTTGGACATTTAG[C/T]CACACACAGGATGTC	4703
rs532891421	snp	A/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151489083	GGATTTATATTGGAA[A/T]TGAATGCATTGGTTT	4703
rs532934712	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151645094	CGGGACCACCGTCCT[A/G]TATGTGTGCCTTTGT	4703
rs532945473	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151564437	GGATTATAGGCGTGA[C/G]CCACCATGCCCAGCC	4703
rs532945852	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151607322	CCACCGATGTATCCA[A/C]GCACTCATTTAAAAG	4703
rs532950615	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151698044	GCACTCCAGCCCGGG[C/T]GACAATGCGAGACTC	4703
rs532955484	snp	A/G	0.00438332	0.0466095	intron-variant	NEB	GRCh38.p7	2:151556371	CTCAGGTAAACTTCA[A/G]GGGTGTGTGTCTGTG	4703
rs532986882	snp	C/T	0.000759821	0.0194765	missense, intron-variant	NEB	GRCh38.p7	2:151606665	TGGCATCTGCCCTTA[C/T]GTCATAGCCTTTCTG	4703
rs532996835	snp	A/G	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151578733	GGAAGGAGGGAAGGA[A/G]GGAAGGAAGGAGAGA	4703
rs533027587	snp	A/G	0.000314739	0.0125407	missense, intron-variant	NEB	GRCh38.p7	2:151614536	CATCCTTAATGTTCC[A/G]GGCCCCAATATGGTG	4703
rs533047516	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151621829	AGTAATTGCCAACAT[C/T]GGTATTCAATAAATC	4703
rs533060176	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151540021	CAGGATTTGAATCCA[C/T]GTCTGGCTGACTGCA	4703
rs533080752	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151624198	TGGGGGATGAGTGCA[A/G]TTTTGCTACATTAAT	4703
rs533092252	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151714403	ATTTCTTGCTCCTCA[A/G]CAGAATTCCTCTTCT	4703
rs533102466	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151620196	TAAAATGGACAATTT[C/G]TGTTATTTAATAGGT	4703
rs533137797	in-del	-/C	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151554363	CCCAGGAGTTTGAGA[-/C]CAGAGTGGGCAACAT	4703
rs533166341	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151571500	AATTCAATTCAGTTT[C/T]GTAACCTTCAGAATT	4703
rs533225671	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151728203	ACACTTCAAAGTAGT[C/G]GGGGGGAAATTGGCA	4703
rs533233215	snp	A/G	9.94547e-05	0.00705106	missense	NEB	GRCh38.p7	2:151548334	CATTGTTGACTCTCC[A/G]GACGTGGACAAATGG	4703
rs533243756	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151644203	GGCAAATTACAAAGC[A/G]CATTAACTCTAAATA	4703
rs533246582	snp	C/T	6.70443e-05	0.00578945	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151526185	GTTGCTGACAGTCTT[C/T]GCCAGCAGGATCTGA	4703
rs533260992	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151637502	CAGCCAAAAAGTTCT[C/T]TTCTTTTTAACATCA	4703
rs533274709	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	NEB	GRCh38.p7	2:151736262	CAGTAAGCATCCCTG[C/T]ACATTACCTTTGTAT	4703
rs533286934	snp	A/G	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151491378	CTCTTCCCTTTGCCT[A/G]TGTATTTTATGTATT	4703
rs533289457	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151723791	GTCATTATTTGTCAT[G/T]GTTTATTAATAGCAC	4703
rs533289804	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151615779	TGTCCGTAAAACACT[A/T]TTTAAAAAATAGTAT	4703
rs533303342	snp	A/C	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151486029	ATGACTGACTCCACA[A/C]ACTTAAGTTGAACAA	4703
rs533345768	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151690408	GTCCTACACAAATAG[A/G]TGCTTTTGTTGTCAC	4703
rs533368725	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151628021	CTAATGGGCAGTAGT[C/G]TAATGCGAAGTCTCA	4703
rs533374072	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151556256	CAATTTACTGAGTCA[C/T]TAGCATTTAAATGAG	4703
rs533374837	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151577041	GACTTCTGAATAATA[A/T]TTAGGTTATCATCAT	4703
rs533383355	snp	A/T	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151690972	TCACTTCTCTGTCTG[A/T]CTCTCTCTCTCTCTC	4703
rs533393007	snp	C/T	1.7585e-05	0.00296517	missense	NEB	GRCh38.p7	2:151567184	TCACTCTGTAGGTCA[C/T]AGGCCTTTCTTGCCT	4703
rs533393621	snp	C/T	6.62509e-05	0.00575509	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151505558	CTTGTCCTATTGCTT[C/T]CTTATACTTCACCTG	4703
rs533407732	snp	C/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151526514	TTCACAGCACGCTCA[C/G]ATATGCCATTTGTCC	4703
rs533428599	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151576684	CTACAGGCACGTGCC[A/T]TGATGCCTGTCTAAT	4703
rs533437385	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151658895	GCCCAACCCCATCCA[A/C]AGTCCTACTCCAACT	4703
rs533439732	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151656889	ATTTCTCTTAATGCT[A/G]CCCTGAGAAATTATT	4703
rs533459664	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151643087	TTCTTTTATACAAAC[A/T]GACTTCAGTGTTTCC	4703
rs533478122	snp	C/T	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151649872	TATACTCTACCCCAA[C/T]AAAAAACATCTGGGT	4703
rs533482697	snp	G/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151531628	GGCCACAACAATTCT[G/T]TATTGGGGAGGAGAA	4703
rs533494950	snp	A/C/T	3.45795e-05	0.00415798	missense	NEB	GRCh38.p7	2:151570331	ATCTTGTTGTCATCC[A/C/T]TGGCTGTGAGGGTGC	4703
rs533511481	in-del	-/TAGG	0.00517822	0.0506191	intron-variant	NEB, RIF1	GRCh38.p7	2:151520441	ACATAAAAATAAGTT[-/TAGG]TAGGCAGAGGGCTAA	4703
rs533529606	snp	A/T	0.00438332	0.0466095	intron-variant	NEB	GRCh38.p7	2:151546892	TCTTAGTTTACTTGC[A/T]CCCAAATAAGTCATG	4703
rs533578801	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151563393	ACACAAAGCAGTCAC[A/G]GTGTTAAATAGTCAG	4703
rs533601461	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151670861	TTTCCCATGTTCAAG[A/G]TCCCAGTTGCCTCAA	4703
rs533613637	snp	A/G	0.000399281	0.0141238	missense, intron-variant	NEB	GRCh38.p7	2:151629640	CATTGGCAAGTTTGT[A/G]TAGAGTCTATGAAAA	4703
rs533617088	snp	A/C	0.0263992	0.111815	intron-variant	NEB	GRCh38.p7	2:151594847	TACTGAAGGAACCTC[A/C]GGTAGGGAGAGGTCA	4703
rs533636180	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151704830	GTCTTCTGCGTCGCT[C/T]GCTCACGCTGGGAGC	4703
rs533644712	snp	C/T	0.479502	0.0991411	intron-variant	NEB, RIF1	GRCh38.p7	2:151531308	TCTCTTTTTTTCTTT[C/T]TTTTTTTTTTTTTTT	4703
rs533657837	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	NEB	GRCh38.p7	2:151735196	CTCCTGGCTCCCAGA[A/C]GCAACGTGTGAATGC	4703
rs533667658	in-del	-/T			intron-variant	NEB	GRCh38.p7	2:151720668	AGATAGGAGATTAAC[-/T]TGTCTTCTTGGAAAC	4703
rs533697294	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151728214	TAGTGGGGGGGAAAT[G/T]GGCAATAAACTATTT	4703
rs533701247	snp	A/G	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151510196	CAGGGAGGTTTGAGG[A/G]GTTTCTTCAGACCCC	4703
rs533746329	in-del	-/AAAT	0.00517822	0.0506191	intron-variant	NEB, RIF1	GRCh38.p7	2:151501966	TACATAGCATACAAA[-/AAAT]AAATAGCCAAGACAA	4703
rs533748763	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151568828	ATACAGTGCCGTATT[C/T]GAATAGCGTCTTCTT	4703
rs533759930	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151686880	GAGTTCACCAAAATT[C/T]AGGCAAAAGGCATGA	4703
rs533761507	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151569955	CCATACTATAAGGTC[G/T]CACTAATATTAAATT	4703
rs533774197	in-del	-/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151640932	TAGAATTTAGAATTT[-/G]TTTTTAAAATATTTA	4703
rs533775799	in-del	-/A			intron-variant	NEB, RIF1	GRCh38.p7	2:151488157	CGAGGGGAATAATTT[-/A]TCAGTGAATTTTAGA	4703
rs533777948	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151656681	AGTTCTTATTACTCT[C/T]CTCATTTTATAGATG	4703
rs533799220	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151569451	ATTGGTCTCATGAAG[A/C]AATACAATGTAAATG	4703
rs533811764	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151490837	ATAAATAGTAATATT[C/T]ACATTCAGACTCCAT	4703
rs533819821	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151604455	AATTGTACAGAATAT[G/T]TTAGGTTCTATTAAG	4703
rs533823410	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151497229	AATCTGCACCCTCTA[A/G]AGAAGCAGGGACCTC	4703
rs533834439	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151612868	AAACGACGTCTTTTT[C/T]GTATGCTTCTATGTA	4703
rs533838343	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151635470	CCAGCACTTTGGGAG[C/T]CTGAGGCAAGTGGAT	4703
rs533840503	snp	A/T	0.00318978	0.0398085	intron-variant	NEB	GRCh38.p7	2:151689975	CTATCTTGAGAAGGA[A/T]GTACTACTCTCTAGG	4703
rs533857454	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151532129	CGAGACGGAGTCTTA[C/T]TCTGTCACCCAGGCT	4703
rs533898172	snp	A/G/T	0.000645706	0.0179567	missense, intron-variant	NEB	GRCh38.p7	2:151633935	CAATATGGTGGCCAA[A/G/T]TTGCTTGCAGTAACC	4703
rs533911309	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151561523	TGAGATTTTGGCCAT[A/T]TTGTTGCCTTTTCCA	4703
rs533916749	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151730467	GATGCAGAAAGGAAC[C/T]GGTTGACACTTGGTT	4703
rs533918654	snp	A/G	6.00691e-05	0.00548005	intron-variant	NEB	GRCh38.p7	2:151561347	TCATCAAAAATGGTA[A/G]CATACAGGTCTGTCA	4703
rs533939803	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151674690	GAATCCCTCATAGCA[C/T]ATACTGCTTTAGGAA	4703
rs533969387	snp	G/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151517266	GACAGAGAACTTCTG[G/T]AAAAACAGGCGAAGA	4703
rs534008092	snp	A/C	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151524990	TATCTTTCTAAAAGT[A/C]CCCATTAAGCACAAT	4703
rs534018522	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151511768	GGAAGATGATGGAGA[A/G]TTATTCATCATGAGG	4703
rs534018659	snp	C/G/T	0.000117722	0.00767128	intron-variant	NEB, RIF1	GRCh38.p7	2:151519790	GCAAATGCAAACATC[C/G/T]AAATTATTCCTGGAC	4703
rs534028054	snp	A/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151640758	TTTATTAAAAAAAAA[A/T]TTTTCCCTGAATATG	4703
rs534043031	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151524167	GAAAAGGCCCTCAGT[A/G]CACTTTTTATAACTC	4703
rs534044088	in-del	-/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151656855	GAAGATGAAAAAAAA[-/G]AAGGCAAAAAAACAG	4703
rs534067782	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151688466	GGGCAGCATATATAG[C/G]TAAGGCATTAGTGCT	4703
rs534069288	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151487252	TTTCTCAAAGCTATC[C/T]TCCACAGTGTTAAAA	4703
rs534101469	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151656644	AACTGAATACAACTC[G/T]CCCTTGTGAGGTAGA	4703
rs534108860	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151655034	TTGATTTCCTGCTTG[A/G]TATCAAGCACAATGA	4703
rs534108954	snp	G/T	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151642230	TTGGTTCATACAGCA[G/T]AGGTTGGGTTTTGAA	4703
rs534113128	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151668859	AAGCCTGTATTAAGC[A/C]AAATTTTATTGCCGC	4703
rs534115160	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151660279	CCCAAAGACTAGGAT[C/G]CCTAAAAAATACTCT	4703
rs534124991	snp	C/T	0.000399281	0.0141238	missense	NEB	GRCh38.p7	2:151690731	AAAGCACTTACATCA[C/T]TAAGCTGTTTCGTGT	4703
rs534143040	snp	A/C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151669253	TACGAGACAAATACC[A/C/T]ACTCTGTCATAAGGG	4703
rs534152855	snp	A/G	0.00318978	0.0398085	intron-variant	NEB	GRCh38.p7	2:151662889	ACCTGTGCCATGGCT[A/G]CTTTCATTCAGGCAC	4703
rs534153627	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151641304	GTGTCATTAAATAGT[C/T]TTTGCACACATGACT	4703
rs534167667	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151635168	GTAAGTGAGACAATG[C/T]ATATAAAGCTCTTAG	4703
rs534172800	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151719620	CAAGGCACAGTGACT[C/T]ACGCCTGTAATCCCA	4703
rs534213069	in-del	-/AG	0.000110065	0.00741759	intron-variant	NEB, RIF1	GRCh38.p7	2:151494113	GCAGGCCAAACTGCA[-/AG]AGTTATTTTGCAAAA	4703
rs534222901	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151517927	AATTTTGTAAATTCC[C/T]AGAACTGCTTTCAGT	4703
rs534227206	snp	G/T	0.00119737	0.0244387	intron-variant	NEB, RIF1	GRCh38.p7	2:151510200	GAGGTTTGAGGAGTT[G/T]CTTCAGACCCCCAAT	4703
rs534245725	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151719331	ATCTTTCTAATCTTC[C/T]GTGACACAACTGTGA	4703
rs534281462	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151547994	CAATAGTTGGTGTAG[A/G]AAACCAGGATCATGA	4703
rs534292082	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151553769	GGTGAGTTTGCTGCC[C/T]TCTGGGTGGGGCCGT	4703
rs534292858	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151686256	AAGATTCTTTTTAAA[A/C]AGCCATTCATATTCT	4703
rs534330275	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151679656	GACTTTTGGGTCATC[A/G]TCAGACCCCAAGCCC	4703
rs534335738	snp	C/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151504507	ACAAGGAAATCTGTA[C/G]CACAGAGTATAAGCA	4703
rs534354953	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151522081	CAAGTGGCAGCCCCC[A/G]GGGTTTATAATCCCA	4703
rs534356975	snp	A/G	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151513781	GTAAATCCACATAAC[A/G]CGCCACCCCAGTTGT	4703
rs534378316	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151496688	TTAGAACTCAGTGTT[A/G]TTATCCACACAAACG	4703
rs534393321	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151521423	CATAAAGAAGTGGAA[A/G]GCCTGCTAAGGAAGG	4703
rs534407315	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151554832	TCTAGGTATGTGGAA[A/G]TGCACTCTATGATGT	4703
rs534420795	snp	G/T	0.00636936	0.0560724	intron-variant	NEB	GRCh38.p7	2:151645210	ATTGAGGTGCTGTTT[G/T]TCAATTCACATGGAC	4703
rs534436549	snp	C/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151527787	GGGACCCTGTGGTCC[C/T]GAAATAGAGGCTAAA	4703
rs534443920	snp	C/T	6.63724e-05	0.00576036	missense	NEB	GRCh38.p7	2:151546386	GGACCATGTCAGGAG[C/T]GTCATACAGGAAGCA	4703
rs534454973	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151609392	CATAATTATTTATAC[G/T]AGCCATGAATAATAA	4703
rs534467862	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151510807	GAACATATCCCCCTC[A/G]GATAAGAGGAGACTA	4703
rs534475193	snp	C/T	3.31181e-05	0.00406914	missense, intron-variant	NEB	GRCh38.p7	2:151627654	TCTTGGCTAACACCA[C/T]TCCCAGCATGTCCAC	4703
rs534476142	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151544096	AGTGGCTTGGATCAG[C/T]ATTTTATCAAGCCTG	4703
rs534479847	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151726066	TTTCTGCTGAATACA[A/C]AATGAATTCTTGCTT	4703
rs534494008	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151672982	ATGACACATTCTAAA[C/T]ATAAGGCCAATATCT	4703
rs534498474	snp	A/G	1.69329e-05	0.00290967	intron-variant	NEB	GRCh38.p7	2:151675255	TTTATTGTCAGGTCC[A/G]AATTTCACATCCCAG	4703
rs534519331	snp	C/T	1.66582e-05	0.00288597	missense	NEB	GRCh38.p7	2:151551779	GGGCCCGGTCCAGAT[C/T]CACGGTTTTGGTAGT	4703
rs534525035	snp	A/C	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151634622	ACTCCAGCCTGGGTG[A/C]CAGCAAGACTCCATC	4703
rs534531948	snp	A/C/T	6.62464e-05	0.00575495	missense	NEB	GRCh38.p7	2:151666286	CCCTTTTTGTACTCA[A/C/T]GATCAGACTGGATTT	4703
rs534560842	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151630616	GGAGTGTTAAATGAA[A/T]GAGCCACATGCACCA	4703
rs534563062	snp	C/T	0.00119737	0.0244387	intron-variant	NEB, RIF1	GRCh38.p7	2:151500922	GATTTCTTTTGGTTT[C/T]AATATGGAGCAATTT	4703
rs534585372	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151726365	CCTGTCTTAGATTAT[G/T]TAAGGCTCTGAACTA	4703
rs534606943	snp	A/C	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151514639	TAAGGTAATATTCAA[A/C]TAAAAAATTAGAAGA	4703
rs534627855	snp	A/C	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151572608	TGGAGTGAAGTGGCA[A/C]GATCTCAGCTCACTG	4703
rs534643907	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151729749	AGGTGACTGCACTAG[C/T]TCGGTTGATTTGGAA	4703
rs534646949	snp	C/T	0.000182151	0.00954161	missense	NEB	GRCh38.p7	2:151672502	TTTGCAGCTGTGATG[C/T]TAACCATGTCCCCAG	4703
rs534654639	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151722271	CCTCCCGCAAATCCA[A/G]TGGTCATGTAAGAAA	4703
rs534694376	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151663934	GCTAGGTGATGTGAG[C/T]TTTGTCTTAGATGAA	4703
rs534707716	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151616532	AATCCCGTCTCCACT[A/G]AAAATACAATAATTA	4703
rs534711644	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151557100	TTTTTGAAAAGATCA[A/G]CAAAATAGATAGACT	4703
rs534723016	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151683937	GTGGACCTTGAGGAC[A/T]TTTTGCTAAGTGAAA	4703
rs534757980	snp	A/G	0.00358779	0.0422022	intron-variant	NEB	GRCh38.p7	2:151685660	AAACCAAATGTCCTG[A/G]CTGGGCCTCAAGGAC	4703
rs534770042	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151646239	CTATAAAGTCTCTAA[A/T]ATAAGAAATAATAAT	4703
rs534774975	snp	A/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151720737	TTTTCAACTTCGCTG[A/T]TTGTTCCCTCATCCT	4703
rs534775049	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151708235	AAAGTCCCTCTTTAC[C/T]CAGTTTTTCATTAGC	4703
rs534781325	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151552495	AGCAAACTGCTTGAA[C/T]GCATCAGGTTTCAGG	4703
rs534797175	snp	A/C	0.00136824	0.0261199	intron-variant	NEB, RIF1	GRCh38.p7	2:151494265	AAACCTATGGGAATC[A/C]AATGGGTCCAAAAAG	4703
rs534811786	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151721436	AGACCTCATTTTACC[G/T]GTGTCCCCTTGTTCA	4703
rs534819552	snp	C/T	0.00358779	0.0422022	intron-variant	NEB	GRCh38.p7	2:151678547	CTACCAATTACATTG[C/T]GCTACTAGAGTACAA	4703
rs534840784	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151659457	AGGCATGCACTACCA[C/T]GCCTGGCTAATTTTT	4703
rs534845823	snp	A/G	1.6563e-05	0.00287771	synonymous-codon	NEB	GRCh38.p7	2:151563660	ACCAGGGAATTCACC[A/G]ATCACTTTTCCAGCC	4703
rs534852023	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151616852	TTGTGCTTATTTTTT[C/T]TTATTTTGCTGTGGA	4703
rs534861704	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151625459	TTACATGAGGATTAA[C/T]TTCATAATTCTCACA	4703
rs534886159	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151486146	TCCAGAACATATGAC[A/G]AACTCCTACAACTCA	4703
rs534886343	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151651225	AAATCTAATGTAATT[G/T]AGTATCAAGAGAGGT	4703
rs534894362	in-del	-/TA	0.0349115	0.127424	intron-variant	NEB	GRCh38.p7	2:151572507	TATATATTGAATATT[-/TA]TATATATATATATAA	4703
rs534898543	snp	C/T	1.73773e-05	0.0029476	utr-variant-3-prime, intron-variant	NEB, RIF1	GRCh38.p7	2:151485749	CAGACAAGTGTGATG[C/T]TTTGAAATGCCTAAA	4703
rs534898649	snp	C/T	0.000234811	0.0108328	intron-variant	NEB, RIF1	GRCh38.p7	2:151493342	TATTTCTTTTTAGTC[C/T]TAGAAAATACCGAGC	4703
rs534921943	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151651833	TTAACTTCAACATAA[A/G]CAATCTGACAAAATT	4703
rs534933139	snp	A/G	0.132751	0.2208	intron-variant	NEB	GRCh38.p7	2:151607768	TGTGTCAGCTTGGCT[A/G]GGGCATGGTACCCAG	4703
rs534951410	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151615926	GGTAACTAAATTTCT[A/C]GCAAGAAAAACTCTA	4703
rs534976589	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151714066	CTTTCTACATAAAGA[C/T]CAGACAGACCCACTA	4703
rs534988166	snp	C/T	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151615029	TCTCAGTCAAGGATA[C/T]GTGTTACATTTAGAT	4703
rs534992315	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151523429	AAGTCAGTCACTCAC[A/G]ACAACCAAATGTATA	4703
rs535039142	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151707250	TTCTGTTTCTGGCTT[A/G]GGGACAGATATAAGA	4703
rs535041729	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151664449	TACACACAAGCTTAG[C/T]GCATTTGTTCTTACT	4703
rs535044327	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151563398	AAGCAGTCACAGTGT[C/T]AAATAGTCAGGGAGA	4703
rs535044394	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151535592	AAAACTTAGGATGGC[C/T]TTCCTGTCATTCTGT	4703
rs535064978	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151644395	AGATTTTGTTCAATT[A/T]AAAATTAAATTGAGA	4703
rs535084521	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151512994	TTGTTCATAGTTTTA[C/T]ACCAAAGAGTGAGAT	4703
rs535113713	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151685571	TCAGATTGCAGCAGT[C/T]AAAAGACTTCACAGG	4703
rs535125329	snp	C/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151512463	TCCTAGAAGCTGGGA[C/T]TGGCGTGCACCACCA	4703
rs535169903	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, intron-variant	NEB, RIF1	GRCh38.p7	2:151485687	AGAACTTAGGTAACA[A/G]TGGAGAGTCTAAACC	4703
rs535170041	snp	A/C/G	4.09243e-05	0.00452336	intron-variant	NEB	GRCh38.p7	2:151677523	TACTTTTCTAAAAAG[A/C/G]TTCCTCCATATCCTC	4703
rs535232428	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151533144	TCTAAGGAATCTATT[C/T]CTTTGAGGCAAATAC	4703
rs535236430	snp	A/G	6.62866e-05	0.00575664	synonymous-codon	NEB	GRCh38.p7	2:151692062	CTTCAAACTTACATC[A/G]CTGTTTTGAGCTGCA	4703
rs535255941	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151559001	TATCAGAGTGAAAAG[A/G]CAACCTACAGAATGG	4703
rs535289921	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151606879	TTCCTCTGTGGTGTA[C/T]AGGATACTTCTGGTT	4703
rs535323610	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151542793	TTCTTAATGCTCAAA[C/T]CTATTCTTCATAGAA	4703
rs535347765	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151534877	GAAATCTACTGAAAG[C/T]GAACTGAATCAAATG	4703
rs535365871	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151541750	GTCAAAACAAGAGAC[A/G]TTCTCTAGCCTGTCC	4703
rs535370004	snp	C/T	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151697832	AGCACTTTAGGAGGC[C/T]GAGGCGGGCGGATCA	4703
rs535373507	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151513718	CATTAAAAGAAAAAA[A/G]AAAGGTACCTAAATG	4703
rs535402051	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151717917	GGAATGCAGTAGCGC[A/G]ATCTCGGCTCACTGC	4703
rs535404281	snp	C/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151637497	GAAAGCAGCCAAAAA[C/G]TTCTCTTCTTTTTAA	4703
rs535412981	in-del	-/C	0.00143233	0.0267229	intron-variant	NEB	GRCh38.p7	2:151569420	CCCTGGTCATGTGGT[-/C]CTAGTTAGCCTATCC	4703
rs535453399	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151571035	TTTGAGACGGAGTTT[C/T]GCTCTTGTTGCCCAG	4703
rs535470587	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151728692	GGTTAAAAATAATGC[A/G]TGTAAGAAAAAAAGA	4703
rs535487481	snp	A/G	0.000175562	0.0093675	intron-variant	NEB	GRCh38.p7	2:151562850	GAAAGGGGTTTAAAT[A/G]TAAATTATTCAGATC	4703
rs535523032	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151619040	TAGAATTTTCCCATC[A/G]GTAAGTATAAAATGT	4703
rs535527430	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151512404	AGTCACAGCTGACTG[C/T]AGCCTCAACCGCCTG	4703
rs535537123	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151628359	GGTCTGGATTATATT[C/T]CCATACTACAAGCCC	4703
rs535571812	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151691342	CTTGACCACCCAACC[C/T]AAGACGCCCATCCAG	4703
rs535581703	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151649926	GAAAAACAGTTTGTT[C/T]GATCATTTTCCCATT	4703
rs535644664	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151541668	CCCACTGCAACGATT[G/T]CAGTTTCTTCCCAAT	4703
rs535660251	snp	A/T	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151664999	GAAATAACAAAAAGA[A/T]GGGCCAAGTAAACTA	4703
rs535663567	snp	A/G	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151664338	AATAATGAACAGATG[A/G]TTAGAGGGTACTTGG	4703
rs535682829	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151657881	AGAGAGTGAGACCCA[C/T]TGTTTTTCATATTGT	4703
rs535683841	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151715130	GCAATGCTTTCAAAG[C/T]ACCCAACACTGTCAC	4703
rs535691730	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151623500	TAGATTGAATTAAGG[A/G]TACCGGACTAGTATC	4703
rs535702519	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151614785	CAGTCACACCACAAG[C/G]AGGTGGCAGCATGAG	4703
rs535729072	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151630578	ATGTAATATTTAACC[C/T]AGAGATGAAAGGTTG	4703
rs535760499	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	NEB, RIF1	GRCh38.p7	2:151497422	AAAATACCAGATGAA[A/G]TAAAAAATTGAAATT	4703
rs535855138	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151555588	TAAGCCATGTTGCCC[A/G]TTAATTAGTGTTCCA	4703
rs535864465	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151540608	CACCATTTATAGTAA[C/T]GAGCTCTCTGATCAG	4703
rs535864508	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151670281	CCCACCTTCCAAAAT[C/G]TGGGGCTAAAATACA	4703
rs535869893	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151510644	CAGTATATTGTTATA[A/G]TTGTTCTATTTTATT	4703
rs535870667	snp	G/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151501924	AATGATACTGAAAGT[G/T]TTCCAAAGGAAAAAT	4703
rs535889614	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151667258	CTAATTTAGTGATAT[C/T]TTAGTATATCATGAC	4703
rs535891183	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151626381	CAGCCTCCCAAAAGT[A/G]TTGAGATTACAGGTG	4703
rs535910091	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151717630	TCCTAGATGTTACAT[A/T]CCATTGCTCTCAGTA	4703
rs535926481	snp	C/T	0.000471019	0.0153391	missense, intron-variant	NEB	GRCh38.p7	2:151625593	GTGTATCAGGCATAA[C/T]ATGGACTTGGGTCTT	4703
rs535935432	in-del	-/AACA	0.0393541	0.134641	intron-variant	NEB, RIF1	GRCh38.p7	2:151512883	GTTTGCAATGTGCAC[-/AACA]AACAGTTGTTGGCTT	4703
rs535953574	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151508756	CAGCTGACTGGCCAA[A/G]GACTGCTCTGAACCA	4703
rs535967336	snp	A/G	1.67086e-05	0.00289033	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151518998	TGTATTCAGGACATG[A/G]TTCATGATCAGAGAC	4703
rs535973187	in-del	-/G	1.67818e-05	0.00289665	intron-variant	NEB	GRCh38.p7	2:151677843	GCTCTGAACTTAATA[-/G]GGGGGGTTTCTTGAG	4703
rs536003026	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151684338	CGTTATAAATATTTA[C/T]GTTAAATCATATATT	4703
rs536004370	snp	C/G	0.0146672	0.084371	intron-variant	NEB	GRCh38.p7	2:151559840	GAAATACCTAATGTA[C/G]ATGATGGGTTGATGG	4703
rs536014958	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151489388	ATATATGTGGGCACA[C/T]TGCATACATCTATAC	4703
rs536027296	snp	G/T	0.000399281	0.0141238	downstream-variant-500B, intron-variant	NEB, RIF1	GRCh38.p7	2:151484873	AGTGCCTGGCATAGA[G/T]GTGTACGTTGGTCAT	4703
rs536035064	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151654385	TATCAGGCATATCAC[A/G]TATCTTTCTCACTGC	4703
rs536051621	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151577340	GCCTGTCTTTCAATT[C/T]GTAGTCTCATCAGCC	4703
rs536056198	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151541129	CTGATTTTTGCGTGA[C/T]TGCATGAAATACAGC	4703
rs536088464	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151605999	GTTTGTTTGTATTTT[C/T]AGTAGAGATGAGGTT	4703
rs536089037	snp	G/T	0.000185557	0.00963038	intron-variant	NEB, RIF1	GRCh38.p7	2:151491805	AGTGATCAGAACAAG[G/T]GTTCTTGGAGTTTTC	4703
rs536092134	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151583231	TTTCTACCTAATTAC[A/G]TAGAATAAGAGACTG	4703
rs536096331	snp	C/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151488714	ATTTTACATCTAAAT[C/G]TTTGGTACAGCTACA	4703
rs536101098	snp	A/C	0.000399281	0.0141238	synonymous-codon	NEB	GRCh38.p7	2:151663764	TGACTGCATCTTGGC[A/C]ACTTGCATGAAGTGC	4703
rs536114462	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151660630	CAAACTTTTTCTGTA[A/T]AGACAGAAATTCCTT	4703
rs536116098	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151613987	TGCTGATGTCTTAAA[A/G]TATTTATGCTCATCA	4703
rs536129128	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151610703	GAAAGGAAATTGTTA[C/T]GGTGGAAAAAGCATT	4703
rs536145124	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151537073	TTCTCAGTGCTAATT[A/C]TCTCTGGGTACAGGT	4703
rs536150202	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151618181	GAAGGTATCATAATG[C/T]TTATTATTATCTTTA	4703
rs536152996	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151621167	AAGAACTCTTTCTTT[C/T]ACTTTCTGTTTATCC	4703
rs536192602	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151605362	TGACAAGTGCAACAT[A/T]AGGTCAAATGATCTC	4703
rs536199831	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151699237	ATGGTGTATATGTGC[C/T]ACATTTTCTTAATCC	4703
rs536205101	snp	G/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151534813	AAATATATCAAGATT[G/T]TATTCATAGGAAGCT	4703
rs536220078	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151553273	TCTGCTCCTAGCAAC[C/T]TTCTCCAGCTCAGCC	4703
rs536240414	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151673859	GGGCCTCAGCCTCCC[G/T]AGCAGCTGGGACTAC	4703
rs536243403	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151579048	ATTGCACCACTGCAC[C/T]CCAGCCTGGGTGACA	4703
rs536247366	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151659351	ACCCAGGCTGGAGTG[C/T]AGTAGTGCAATTATG	4703
rs536328500	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151632891	ACTATCTTTTCTGTG[C/T]AGGCAAAGCCTTTCT	4703
rs536329294	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151715969	ATAAGGCAAAAGAAT[A/G]TTTCCTTAGTAAAGT	4703
rs536356221	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151527757	AGCTAGTCATCCACT[C/T]AGAGGTCATCTGTTG	4703
rs536375355	snp	A/G	1.67094e-05	0.0028904	missense	NEB	GRCh38.p7	2:151551757	CTCTGGAGCTTGTAT[A/G]CATGAAGGGCCCGGT	4703
rs536400042	snp	A/G			intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151499016	TTTAGGTTCAGATCA[A/G]ATTTGCCAAAGCAGT	4703
rs536402096	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151673160	ATTAAGGAGCCACAG[G/T]AAGGACCTGCTGTGG	4703
rs536410281	snp	C/T	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151694137	AATTTGCAGTATTCA[C/T]TGGCATCAAAGGCAT	4703
rs536418256	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151687171	GAATACAATCAATAT[G/T]CTATTAAATATTAAT	4703
rs536426422	in-del	-/AG	0.226843	0.248925	intron-variant	NEB	GRCh38.p7	2:151591464	AGCGTTTCTGCAAAC[-/AG]AGAGTGCAATGCCAC	4703
rs536443205	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151661696	AGATTACCCAGAGAA[C/T]GTCCTGGTTTGAAAT	4703
rs536447142	snp	A/G	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151591724	AAAAACATATTGCTT[A/G]GCTTTTACAAGGAAA	4703
rs536449918	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151574409	AATGAGAAGTTTGGT[C/G]ACTGAGGATGAGTTG	4703
rs536483432	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151611378	AAGTCATAGCAGATA[C/G]TCAACGATTTTTTGG	4703
rs536508378	snp	A/C	0.00438332	0.0466095	intron-variant	NEB	GRCh38.p7	2:151572763	ATCACGTTGGCCAGG[A/C]TGGTCTCGAACTCTG	4703
rs536508687	snp	C/T	0.297521	0.245442	missense, intron-variant	NEB	GRCh38.p7	2:151579592	TAGGGTCTTCCTTGG[C/T]GCTGCGACAGCCAAT	4703
rs536529073	in-del	-/CCT	0.00119737	0.0244387	intron-variant	NEB, RIF1	GRCh38.p7	2:151489555	AGATGCACCACCACA[-/CCT]GGCTAATTTTTTGGT	4703
rs536560975	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151502600	AGAAAGTGATAAATA[C/T]CTATGTTTTAGAGAA	4703
rs536567910	snp	C/T	0.00755907	0.0610114	intron-variant	NEB	GRCh38.p7	2:151704213	GAGGAGGCAGTCTGC[C/T]CGTTCTCAGATCTCC	4703
rs536578561	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151693334	ATAGGGAAGCGTGTG[C/T]CATGGTGGTTTGCTG	4703
rs536581512	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151546145	CAGGAGCAAAAACAA[C/T]TGTCATTTAACTAAG	4703
rs536660515	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151673026	GGTTTCATAGGTTTC[A/G]ATTTAATATGTTATT	4703
rs536677256	snp	A/G	0.000224067	0.0105822	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151508078	GTCTCATAATACGAC[A/G]TGGACTTCTCAGCAT	4703
rs536678090	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151652818	TCACACAAAAAGAAA[C/T]GAGGTACTATCAAAT	4703
rs536684179	snp	A/G	0.000399281	0.0141238	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151494162	TCTCAAGACAATACC[A/G]AGCTAATGTTTTCTT	4703
rs536689277	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151486383	GTGGAGAAATTGGGT[C/T]CTTCATAAACCACTG	4703
rs536694687	snp	C/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151493578	GCTATTAAAATGTTA[C/T]GGTAGGAAGCAAAAG	4703
rs536698421	snp	A/G	0.00199481	0.0315187	intron-variant	NEB, RIF1	GRCh38.p7	2:151500851	TGATCTGCCTGCCTC[A/G]ACCTCCCAAAGTGCT	4703
rs536700837	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151658741	AGGGCTGTCTAAGAA[C/T]GAAATTCTAGGACTC	4703
rs536730527	snp	C/G	0.000169866	0.00921434	intron-variant	NEB, RIF1	GRCh38.p7	2:151514788	AATTATTTGGATTAA[C/G]AGGGAAAGAAAAGAC	4703
rs536735721	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151639121	TTCATATTGCATAAA[A/G]TTTGACATTTATGAT	4703
rs536736014	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151631389	CTTCATCAAGACCAC[A/T]ATATTTAGGGTAAAT	4703
rs536747617	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151556877	AAGCAGTGTGTAGAG[A/G]GAAATTTATAGCACT	4703
rs536758857	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151500063	AATAATTTTGAAAAT[C/T]GTTGCAAGCCTTTCA	4703
rs536762025	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151616292	CACATGTTCCAAACA[C/T]TGGGATTTTACTGAC	4703
rs536768399	snp	A/C	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151706695	ACCCCACAGAACCAC[A/C]AACAGTAAGGCACAT	4703
rs536768661	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151522142	GTAGTATAGGAAAGT[A/G]ATTTTGCATTAATTA	4703
rs536781506	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151543023	ATGTTCTTCTCCCTT[C/T]TATTTGCCTGGAAAA	4703
rs536782479	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151578646	GGGCAAGGGAAGGAG[A/G]GAAGGAGGGAAAGAG	4703
rs536803104	snp	A/C	0.00119737	0.0244387	intron-variant	NEB, RIF1	GRCh38.p7	2:151523226	TTCAAATACTTATAC[A/C]ATTCCATTAATTTAT	4703
rs536824060	snp	A/C	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151535970	TGGACTGCAAGGCAC[A/C]GTCATAGCTCACTGC	4703
rs536841560	snp	C/T	0.00835141	0.0640778	intron-variant	NEB	GRCh38.p7	2:151660139	GTGGGGGTACAAAGA[C/T]CTAGCCATTTCAGTT	4703
rs536849721	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151680572	AAATATATGAATTAG[G/T]CATGCTTTATTAATG	4703
rs536867483	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151565682	GCAGGTAGGAGGACA[G/T]GCATAGGTTAGAAGG	4703
rs536875096	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151660563	TGCTATCTCTTTGTT[C/T]TAGCCCATCTTAATT	4703
rs536889870	snp	A/G	0.00119737	0.0244387	intron-variant	NEB, RIF1	GRCh38.p7	2:151494735	CTCACTGCAACCTCC[A/G]CCTCCCGGGTTCAAG	4703
rs536916296	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151653540	AATTTATTACAATTA[A/T]ATAAGTGCAAAATGG	4703
rs536920694	snp	A/G	0.000459918	0.0151574	intron-variant	NEB	GRCh38.p7	2:151617503	AGAGAGAGAGAGAGA[A/G]AAAAATTATTTTGGT	4703
rs536921322	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151645578	TTGGACTTGTGTTTA[A/T]CTGTCAGTCCTTCGT	4703
rs536921930	snp	A/C	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151522391	AACTTCAGAAGAGGC[A/C]GAGGTTTCTTTGGTT	4703
rs536934629	snp	C/T	8.29057e-05	0.00643785	missense	NEB	GRCh38.p7	2:151548321	ACCTCGCTGGTAACA[C/T]TGTTGACTCTCCGGA	4703
rs536945839	snp	C/T	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151638484	ATCTCTGGGGGTTGG[C/T]ACAGATTTGTTCTGT	4703
rs536948198	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151692778	AGTTCAACACCAGCC[G/T]GGCCAATGTGGTAAA	4703
rs536965992	snp	A/G	0.00119737	0.0244387	intron-variant	NEB, RIF1	GRCh38.p7	2:151508623	CTATAGGACTGAGCC[A/G]GCAGTCAGACAGGCA	4703
rs536975021	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151639475	ACTTTATAAAAAAAA[A/C]GAAAAGGTTATGTGT	4703
rs537018767	snp	A/T	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151680528	TGTCAAATGGCTAAA[A/T]GGACAGTCAGCACAA	4703
rs537028649	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151559764	ATGGACACAGGGAGG[A/G]GAACATCACACACTG	4703
rs537031468	snp	A/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151551903	ACCCAGGTTCCTCTT[A/T]AAAAAAAATAACGGT	4703
rs537033983	snp	A/C	6.07995e-05	0.00551326	intron-variant	NEB, RIF1	GRCh38.p7	2:151493480	ATCTAGGCATCAGAC[A/C]GCAGAAAACCAGGTC	4703
rs537047994	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151642061	GAGTGAGAACATGCA[A/G]TGTTTGATTTTCTGT	4703
rs537061302	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151499617	TTATTGTAACTTGAA[C/T]ATATTTATTTCCTGT	4703
rs537062415	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151550844	TCAGACAGGGTTTCA[C/T]CATGTTGCTCAGGCT	4703
rs537063465	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151559198	TGAAAAAATGCTCAT[A/C]ATCACTGGTCATTAG	4703
rs537070329	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151566260	ACAAGTAAATATTCA[C/T]GTATTGGGTAGGGGA	4703
rs537095240	snp	C/G/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151499920	CACCACTGGGCAATT[C/G/T]TGCCTAAATGCAATC	4703
rs537096950	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151624867	GGACTGCAAAGATAT[G/T]CAATGACAAGTTTAG	4703
rs537101142	snp	A/G	0.00318978	0.0398085	intron-variant	NEB	GRCh38.p7	2:151671759	TGAGCTCATCTGGGG[A/G]GCAATATTTTTATCG	4703
rs537107342	snp	A/T			synonymous-codon	NEB	GRCh38.p7	2:151674486	ACTCACATCACTGGC[A/T]ATGTTTCTCGATGCC	4703
rs537118920	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151615103	CAACATCACTGAACT[C/T]TCACTATGAGTCAGT	4703
rs537124764	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151714208	CCAAAGAAGAAAACA[A/G]TTCCCTCTGACCCCT	4703
rs537127403	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151623364	CATCCCTCTACTTTA[C/T]ACTGTTCAGTGTACT	4703
rs537133652	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151722102	TAGATTCCATTAGAA[G/T]TAAATCCCAATCAGT	4703
rs537167912	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151714799	CTATTTTAGGGAGAA[A/G]GAAGATATGATCCTG	4703
rs537183497	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151687090	TGAAAATTATCATTT[A/T]AAAAATTGTTTTTCA	4703
rs537193914	snp	C/T	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151709566	AAGAACCACTCCTCC[C/T]CTTTTTTACTAATTA	4703
rs537199662	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151702695	GATTGCAACCCCTGC[C/T]TTTTTTTTGTTTTCC	4703
rs537211383	snp	A/G	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151692684	TTTAAAGAAAAATGA[A/G]TTTCGCTAGGTGCAG	4703
rs537229270	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151495077	TTGCTATCCTCTATG[C/T]TCTGCCTCTTGCTTT	4703
rs537240072	snp	A/G	0.000637146	0.0178372	intron-variant	NEB	GRCh38.p7	2:151581466	CTGTGAAAAGCAAAT[A/G]ATGTGTGCTGTCTTA	4703
rs537243517	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151667125	AATACGAAAAACCAG[A/G]AAGAATCAGCAAAAT	4703
rs537255388	snp	A/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151486892	GGGCACCAGCATTTG[A/T]TTGTTTGTTTTAATT	4703
rs537272980	in-del	-/AATA	0.0225045	0.103662	intron-variant	NEB, RIF1	GRCh38.p7	2:151525660	GGGTAGCAGTTTAAT[-/AATA]AATAGGAGAGGCCAC	4703
rs537278235	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151579007	CATCGCTTGAACCTG[A/G]GAGGCGGAGGTTGCA	4703
rs537285801	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151645297	ATCATGCCTAAGGGG[A/T]TATCTCTTCTATGTA	4703
rs537287106	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151618122	GTTTAATATTTTGAA[G/T]TATCACTAAGTAACT	4703
rs537319618	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151486237	ACAAATAGCCAAAAA[A/G]CACACAAAAGGATGC	4703
rs537345128	in-del	-/AA	0.000190862	0.009767	intron-variant	NEB	GRCh38.p7	2:151553813	GGAGGGGTACTTCTT[-/AA]GTCACAGGCTTACAT	4703
rs537348115	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151708085	GCCATCCCCTCCTCT[C/T]AAGCACCAAATCTCT	4703
rs537380305	snp	C/T	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151699088	TCATTGTTCAGTTCC[C/T]ACCTATGAGTGAGAA	4703
rs537451022	snp	A/T	8.28754e-05	0.00643668	missense	NEB	GRCh38.p7	2:151538171	GTGACTTTGCGATGA[A/T]AGACAATGTCTAGGG	4703
rs537470113	snp	A/T	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151658495	GTGGAATCTACAATT[A/T]AAAAAAAAGGTCAGC	4703
rs537472211	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151559177	TTTATGCGGCCAACA[A/C]ATATATGAAAAAATG	4703
rs537480755	in-del	-/GAG	0.00199481	0.0315187	intron-variant	NEB, RIF1	GRCh38.p7	2:151491916	CATGTCTTTTCCTCA[-/GAG]GAGAACAAAGATAAG	4703
rs537485718	snp	G/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151489613	TGTTGCCTAGGCTGG[G/T]CTCAAACTCCTGAGC	4703
rs537508368	snp	C/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151499144	GTTTTACCAAAATGG[C/G]GAAAACTGATTCATA	4703
rs537538598	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151544392	TCAACACAGGCTACA[C/T]ATTATTAAACAGAAT	4703
rs537542648	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151539954	ATATGAAAAGAGACT[C/T]GGAAAAATTAGACAG	4703
rs537551104	in-del	-/AAAG	0.021333	0.101051	intron-variant, utr-variant-3-prime	NEB, RIF1	GRCh38.p7	2:151497398	TCATTATTTTAAAAA[-/AAAG]AAAGATTGAAAATAC	4703
rs537560378	snp	A/G	1.65633e-05	0.00287774	stop-gained, intron-variant	NEB, RIF1	GRCh38.p7	2:151506189	TGTGGTCCTGTGTTT[A/G]TTTCACTCTCATCAT	4703
rs537591141	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151546968	TGCTATTATTTTATT[A/G]CTATAACATTGATTG	4703
rs537596189	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151550098	ATAGCAAGATCCCAC[A/C]TCTATAAAAAATTTT	4703
rs537610307	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151521554	AAAGCAAACCAGATA[C/T]GCAGAGTCAGAGTAG	4703
rs537682041	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151572150	AACATGGTGAAACCT[C/T]GTCTCTATTAAAAAT	4703
rs537703262	snp	C/T	0.00279162	0.0372561	intron-variant	NEB	GRCh38.p7	2:151659327	TTTGAGACAGAGTCT[C/T]GCGCTGTCACCCAGG	4703
rs537703959	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151575866	AGTCCCACTATGCAA[A/C]TTTTAAATTTTCTTT	4703
rs537706011	snp	A/G	0.152778	0.230321	intron-variant	NEB	GRCh38.p7	2:151603816	GGAAGAGTCAAAGTT[A/G]CCCATAAGAGTTTGA	4703
rs537717247	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151578489	ACATGATGAAACCCT[A/G]CCTCTACTAAAAAAT	4703
rs537737064	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151705266	AGAAGAAGCAATGAT[C/T]AGTTTTAAATATGCA	4703
rs537748753	snp	A/G	0.000120564	0.00776321	intron-variant	NEB	GRCh38.p7	2:151695553	TTGTCAGTACATCAC[A/G]TGGTACAGGGCATAA	4703
rs537749540	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151698272	CACACAATTCACCAA[A/T]TTAAAGTATACAATT	4703
rs537769519	snp	A/C	1.65682e-05	0.00287817	missense	NEB	GRCh38.p7	2:151677618	TAACTGGGGAGTCCA[A/C]AATGCTGGTAAATTT	4703
rs537772844	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151534014	TTCATCTTCACCACA[A/G]CACAAGTGAGAACAC	4703
rs537774772	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151613265	CAATTGTTTTCAAGT[A/T]TCTTAGAAAATTTGT	4703
rs537787722	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151689374	CATACCCAGCTAATT[C/T]TTTTATTTTTTTGTA	4703
rs537810047	snp	C/T	0.000481468	0.0155081	intron-variant	NEB	GRCh38.p7	2:151640087	AATAGCCAATAAATA[C/T]TTATCTCTGTATCAG	4703
rs537819135	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151539092	ACTATTGTAAAGATT[A/G]GAGTTATCAGAATTG	4703
rs537819790	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151628333	TGCTGGGGCACTTGA[C/T]TCCCTGAAGTGGTCT	4703
rs537821059	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151687778	ATAAGAACAACAGTG[G/T]AATCCAGTAAAAAAA	4703
rs537831148	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151662681	TCTCCTTGAGAAAAG[C/T]AACTATGCTGACCTT	4703
rs537836623	in-del	-/AATT	0.00557542	0.0525036	intron-variant	NEB	GRCh38.p7	2:151612652	AAACCACCTTAAGGA[-/AATT]AATTACTGCCTGCCT	4703
rs537850384	snp	A/G	0.000399281	0.0141238	missense	NEB	GRCh38.p7	2:151688383	TCACCTTCATGTTTT[A/G]CTTTGTAATTCAGCT	4703
rs537856203	snp	C/G	6.2588e-05	0.00559375	intron-variant	NEB	GRCh38.p7	2:151547383	GCTGAAAGCAAGCCT[C/G]CGTCTTGGTAAGACT	4703
rs537871535	snp	A/G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151574275	CATCGCGCCAGGCAT[A/G/T]TTCTTACTCTTGAGT	4703
rs537878765	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151612072	TTAAAGGCCTGCATG[A/G]GAATCAGGCCTATGA	4703
rs537884087	snp	C/T	0.00398564	0.0444627	intron-variant	NEB	GRCh38.p7	2:151566202	TGATACATTTAGTCA[C/T]GTAGAAGTATGTGGG	4703
rs537901110	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151668714	AAAGCAATGTTTTCC[A/G]TACTACAGACTAGGC	4703
rs537915810	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151654155	TAAAGAATATCAATA[G/T]ATTATTAGGGAAAAG	4703
rs537921520	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151719300	GGCCATGGGGGAATG[C/T]CTCAAGAGGAGAATT	4703
rs537940961	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151702998	TGCAGTGGCTGGTAC[A/C]GGTTGTTGCTTTCCA	4703
rs537951612	snp	C/T	3.31241e-05	0.00406952	missense, intron-variant	NEB	GRCh38.p7	2:151627563	CGAGCATGGATGACA[C/T]CATTCTGGTCGGGCA	4703
rs537954993	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151661228	ATGTTAATCACTAAC[A/G]CTGAAAAAAATAGAT	4703
rs538003303	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151642168	TGTTCCACAGGAATC[A/G]TTGAACTTTGAGTAA	4703
rs538019612	snp	A/G	0.00358779	0.0422022	intron-variant	NEB	GRCh38.p7	2:151689847	AGTGGCACACGAGCT[A/G]AAATGACTTCTGAGT	4703
rs538027877	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151693733	GTTCATATATATTTA[C/T]AATAGAATGATTTAT	4703
rs538032504	snp	C/G	6.67546e-05	0.00577692	intron-variant	NEB	GRCh38.p7	2:151674604	ACAGAAAAGCAAACA[C/G]AATGTCAGCATCTGT	4703
rs538050592	snp	C/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151574780	CCTGTCACCCAGGCT[C/G]GACTGCAGTGGCATG	4703
rs538068134	snp	A/G	0.000416157	0.0144189	missense	NEB	GRCh38.p7	2:151561252	CAGTCACATAGAGGG[A/G]CGTGTCTGTGACCAG	4703
rs538092955	snp	A/G/T			intron-variant	NEB	GRCh38.p7	2:151685415	AGGGCTGTAGACTTA[A/G/T]TTTATTGGCTGTATA	4703
rs538093509	in-del	-/A	0.5	0.000399361	intron-variant	NEB	GRCh38.p7	2:151555871	TTTAAAGGCACCGTT[-/A]AAAAAAAAAAAAAAC	4703
rs538107253	snp	C/T	1.90944e-05	0.00308979	missense	NEB	GRCh38.p7	2:151560642	TCAGGGACAAGGTGC[C/T]GGAAGGCAGGATGTA	4703
rs538132231	snp	A/C			intron-variant	NEB, RIF1	GRCh38.p7	2:151494397	GAAAGTAGTATGTTT[A/C]CTAAGGAAGTTAAGT	4703
rs538146978	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151649402	TGTATAGCATATTAC[A/G]TATAGTATATATATT	4703
rs538167251	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151524957	AGGCATGAGCCACCA[C/T]GCCCAGCCGAGATAT	4703
rs538176117	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151696284	CTTCACTTACTCTTC[A/C]AAACAGCCACAAATT	4703
rs538178591	snp	G/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151531185	AAAGTTTTTTCCTGA[G/T]TGAATATAAAGGAAA	4703
rs538231036	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151575046	TGCCCAGCTGGTCTA[C/T]AGTTTTTAATTTGTG	4703
rs538269978	in-del	-/A	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151697769	CCTGTCAACTGTCTT[-/A]AAAACTGACAATTGA	4703
rs538273174	snp	A/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151731800	ACTGGCATTATTATC[A/T]TAGGGAAGACAATTT	4703
rs538299812	snp	A/C	0.00795532	0.062565	intron-variant	NEB	GRCh38.p7	2:151583178	AATATGTATATGACT[A/C]TGCAAAGGTAACGGC	4703
rs538314913	snp	C/T	0.000710315	0.0188322	intron-variant	NEB, RIF1	GRCh38.p7	2:151502779	TTTTTTTTTTTTGGC[C/T]CCCTAAGAAATACCG	4703
rs538360152	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151534834	ATAGGAAGCTACTGG[C/T]AGTAATTCTTCAGGG	4703
rs538365180	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151621257	TTTGCACAAATCTTT[C/T]ACACGTTATACATTA	4703
rs538368070	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151626502	TATAACTAACTCTTA[C/T]AGACTTCAAACAATT	4703
rs538369739	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151718399	CTATGGTATACTAAT[A/G]CCATTTTGTCTTCAA	4703
rs538372926	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151536835	TTTATATTGGCTGTC[A/T]TATCAGCTTTAATAG	4703
rs538380281	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151657232	TGGGATGGGCTGGAT[A/G]GGTAGGGAAGATGAA	4703
rs538486333	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151567896	CAAGAAAGCTCAAAG[C/T]CCATGGAAGAAAGAC	4703
rs538486421	snp	G/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151575257	GCTGTATGTTTTTTG[G/T]TTTTTTCTCCTTGGG	4703
rs538514382	snp	C/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151489556	GATGCACCACCACAC[C/G]TGGCTAATTTTTTGG	4703
rs538514532	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151517050	CTTTATTTATAAGTA[A/G]ACAACTCTATGTGGG	4703
rs538520038	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151654965	TAGCTGGGACTACAG[A/G]TGCATGTCATCACAC	4703
rs538524105	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151591977	TTTGGGGTGTATAAT[A/G]AAAGGTTTGGTTAGG	4703
rs538524863	snp	C/T	0.00102625	0.022629	missense, intron-variant	NEB	GRCh38.p7	2:151633890	GCATGGACCACATCA[C/T]CTTGGGGTCATCTTC	4703
rs538529215	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151509522	GAGAAAGGGACCTGA[A/G]CTCCCTGGTGTTCCC	4703
rs538552221	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151640725	GTAAAAAGCAATCAC[C/T]AAGCCTAACTTGCTC	4703
rs538554559	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151704616	CGGGAGGGAGTGACC[C/T]GATTTTCCAGGTGCG	4703
rs538573341	in-del	-/TCA	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151698350	CAATTTTAAAACATT[-/TCA]TCATCTCAAAAAAGC	4703
rs538590995	snp	A/G/T	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151631982	TGTAGAACCCCTGAA[A/G/T]CCCTGAGATCTTCAA	4703
rs538609404	snp	C/T	1.65707e-05	0.00287838	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151529264	ATGAACAGCATCTGG[C/T]TCAATGGTGCAGTTG	4703
rs538637730	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151573665	CTTCTCTCACAAAGA[C/T]ATATTATTCTTTTGA	4703
rs538647271	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151546198	ACAGATCACATTAAA[A/G]TGATAATCTGCTCAA	4703
rs538650358	snp	A/G	0.00279162	0.0372561	intron-variant	NEB	GRCh38.p7	2:151687292	TCTGAAGTTCTCTAC[A/G]GCAGTACTTTTGTGA	4703
rs538652431	snp	C/T	0.00279162	0.0372561	intron-variant	NEB	GRCh38.p7	2:151693985	AATCAGTTCAGGGCA[C/T]TGGGTGAATATATAC	4703
rs538665334	snp	A/C	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151661737	GCATGTAATCTTGGA[A/C]TTTTCTTTGATCCCA	4703
rs538695891	snp	C/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151509936	TCTGTAACTGGTTAC[C/T]GGGAGAAGGCCTGGA	4703
rs538704145	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151626888	AATTCAACTGAATCA[C/T]TATACATTGGATAGC	4703
rs538727749	snp	G/T	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151549985	ATTGAAAGTAGTTCC[G/T]GGCCAGGTGTGGTAG	4703
rs538739411	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151535900	AATTAATTCATAGAA[C/T]TAACACATATTCGTT	4703
rs538743682	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151702122	CTTCATTTCGTTATG[C/T]ACCCAGTAGTCATTC	4703
rs538774800	snp	G/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151544813	TGAGAAGGATGAAAT[G/T]GCCTGGAAGCCAATG	4703
rs538780310	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151732266	ACTGTATTTATGTGC[A/G]TTATAGTTCCAAGCC	4703
rs538790617	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151702615	GATCCCTTTACCATT[A/G]TGTAATGGCCTTCTT	4703
rs538803526	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151695400	ACTTATAAGATTGCT[A/G]CACATATTTTGTAAG	4703
rs538809505	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151632962	AAGCTACAGAACAGA[C/T]GTGGGAGTTTTCTCA	4703
rs538816636	snp	C/T	1.65647e-05	0.00287786	missense	NEB	GRCh38.p7	2:151575699	GTAGTACTTACATTG[C/T]TCACATTAAGAGCAT	4703
rs538841644	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151689291	CTCACTGCAACCTCC[A/G]CCTCCCAGGCTCAAG	4703
rs538853596	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151594483	AGGAATTAGATAATA[C/T]GATTTTAGGTCATTT	4703
rs538857403	snp	A/G/T	0.0134861	0.0810011	intron-variant	NEB	GRCh38.p7	2:151702227	TGCACTGTGGTCTGA[A/G/T]AGATAGTTTGTTATA	4703
rs538863332	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151648545	CTGGAGCAACACACA[C/T]TGTACCCACCAAGCA	4703
rs538875676	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151673937	GAAATTTTGGCCAGG[C/T]GTGAGCCACCATGCC	4703
rs538894161	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151724602	TCTTTGGTGACACTG[G/T]GACTTCATGCAGCAA	4703
rs538907698	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151577924	CCATGGTATCTTTAG[C/T]GCTTAGCACAATGCC	4703
rs538919878	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151711173	ACCCAACACAAAATG[C/T]AGCACACAGAAGTTA	4703
rs538925558	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151538782	AAACTTCATTTCATT[A/T]TAATCTTTATCTTTG	4703
rs538931154	snp	G/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151530633	TTTAAGCCACGTGGA[G/T]ACCCATCTGGGGAGA	4703
rs538962069	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151694697	ACCTTTAAAGACTAG[C/T]GGGTAACTAAATACC	4703
rs538990928	snp	C/T	7.36323e-05	0.00606718	synonymous-codon	NEB	GRCh38.p7	2:151687707	CTTCTTGGCTTTGCT[C/T]TTCTCCCAGTCTTGC	4703
rs538993594	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151702953	CAGTTTCTTCCTAGT[A/C]TCGATGGTCTTTACA	4703
rs539008055	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151695884	ACCATGGTAGGACCC[A/T]AAGGGAATGAGGTGG	4703
rs539013258	snp	C/T	0.000205698	0.0101394	intron-variant	NEB	GRCh38.p7	2:151690846	AAAGAAGATGTTCTT[C/T]AATGAAATATCAGTA	4703
rs539013946	snp	A/C	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151581955	ACATAATTTAAAATG[A/C]GTCAGAAATATGGTA	4703
rs539015767	snp	G/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151508524	AAGCTGGAGGGTTAA[G/T]AGTCAAAGACATGAC	4703
rs539039729	in-del	-/TAAAT	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151592270	AAGTGAATTTTATAA[-/TAAAT]TAAAACTAACATAAG	4703
rs539072071	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151646287	AGATTAGTGAATGAT[A/G]CAGTTGGCTTCAAAC	4703
rs539092012	snp	A/G	0	0	upstream-variant-2KB	NEB	GRCh38.p7	2:151734822	GTCATTTGTCCAGTC[A/G]TGGTGGTAAATGTAC	4703
rs539099291	snp	G/T	1.799e-05	0.00299911	missense, intron-variant	NEB	GRCh38.p7	2:151609820	GTACATCACTCTGCA[G/T]GTCATAGGCCTTTTT	4703
rs539103036	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151535509	CTTCACTTGTTCTTA[C/T]TTGTAGTTTGGCAGA	4703
rs539109624	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151494700	GTCACCCAGGCTGGA[A/G]TGCAATGGCACGATC	4703
rs539139958	snp	A/G	0.000432432	0.0146979	missense, intron-variant	NEB	GRCh38.p7	2:151617468	CTTCAGTATATAAGC[A/G]CTACAAAAAAAAAAA	4703
rs539142297	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151532166	CAGTGGTGCGATCTC[A/G]GCTCACTGCAACCTC	4703
rs539166926	snp	C/T	0.00716266	0.059414	intron-variant	NEB, RIF1	GRCh38.p7	2:151500839	CCTGGGCTCAAGTGA[C/T]CTGCCTGCCTCGACC	4703
rs539177919	snp	A/G	0.00119737	0.0244387	intron-variant	NEB, RIF1	GRCh38.p7	2:151522064	GCAATGCCATGTCTC[A/G]GCAAGTGGCAGCCCC	4703
rs539183430	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151541038	ACCACTGAGTATGAT[C/T]CAAGCAAAGCCATGT	4703
rs539213959	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151535230	ACAATGGCAATATCT[C/T]TGAAGCATGAATCAC	4703
rs539238376	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151681972	ATGTGGTGTGTATTA[C/T]GCTGGGGCAAAAGTA	4703
rs539264436	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151732382	ATAAATATAAAATAA[A/G]TGATTAACAGCTTTG	4703
rs539274148	snp	A/T	0.00318978	0.0398085	intron-variant	NEB	GRCh38.p7	2:151678518	AAAATGAAAAGATAA[A/T]TATGTCACAATCTCT	4703
rs539298730	snp	A/C/T			intron-variant	NEB	GRCh38.p7	2:151670520	AAGAGTCCATACAGA[A/C/T]GTGGTCTCAGAATGA	4703
rs539307156	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151563062	CTCTGTTGCCCAGAC[C/T]GGATTGCAATGGTGT	4703
rs539315827	in-del	-/A			intron-variant	NEB	GRCh38.p7	2:151650939	GGCCAAGTTAAGCTC[-/A]ACTTGCTTTTTTTTC	4703
rs539319198	snp	A/G			intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151498657	TCCCACCTTGTTACA[A/G]GGAGGGAAAAAAGTA	4703
rs539335816	snp	C/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151520384	AAAAGTGAGATACTT[C/T]AGAATAATGAGAAAA	4703
rs539347918	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151544458	ACACGGAGAATCAGT[A/C]TGGTGTGGAACAAGG	4703
rs539363010	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151667748	GTTGCCCAGGCTGGT[C/T]TTGAACTCCTGAAGT	4703
rs539367087	snp	A/C	0.000399281	0.0141238	missense, intron-variant	NEB	GRCh38.p7	2:151639302	TAGTTGATTTTGTTC[A/C]TTCTTGCCAACATAA	4703
rs539372339	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151527276	CTCAGTCATTTGTGT[C/T]CAGGCCCAGCCAAAG	4703
rs539377777	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151526704	GCTGGTGCAGTATAA[A/G]TCGAGGACTGTCACC	4703
rs539401306	snp	A/C	2.67813e-05	0.00365923	intron-variant	NEB	GRCh38.p7	2:151642873	TGTATAGAGGCGCTA[A/C]GAGAAACAGAAAAAC	4703
rs539404905	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151513314	ATGTCGAGTTTGCCC[C/T]AGCTCCAAACAGCTA	4703
rs539435670	snp	C/G	1.65811e-05	0.00287929	intron-variant	NEB	GRCh38.p7	2:151554926	GGGCGCATGACCGTA[C/G]TTACATCGATGTTAA	4703
rs539448604	snp	A/C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151577326	GTCCTGATCACACAG[A/C/G]CTGTCTTTCAATTCG	4703
rs539456425	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151571130	CCTTCCTCAGCCTCC[C/T]GAGTAGCTGGGATTA	4703
rs539492726	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151518793	GAGGTGTTACAGACA[A/G]TGGAGAATTGGTAGA	4703
rs539502735	in-del	-/T	0.00438332	0.0466095	intron-variant	NEB	GRCh38.p7	2:151568855	TCTTGGGAATTTGGC[-/T]TTCTTTTTAGCATTT	4703
rs539508810	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151605809	TTCTATTTTTATTTT[C/T]ATTTTTTTTGAAACG	4703
rs539518038	in-del	-/A	0.542788	0.0908276	splice-acceptor-variant	NEB	GRCh38.p7	2:151568419	TCCGGTATTTAATCT[-/A]AAAAAAAAAAAAATG	4703
rs539518293	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151706195	CCAACCACACACACA[C/T]ATTTCCTATGCTGCT	4703
rs539522251	snp	A/T	1.76064e-05	0.00296697	intron-variant	NEB	GRCh38.p7	2:151650149	TAGCAGGCACTATAA[A/T]CTATTTATTTCCAGA	4703
rs539542406	snp	C/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151605010	TCATTACATATTTCA[C/G]TTCACTTTAAAGAAA	4703
rs539546162	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151697004	GTCAACAAGGGAAAA[C/T]AGGATGTTTACTACA	4703
rs539569696	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151641519	AGTTTTTTGTAGAGA[C/T]AGTGCCTTGCTATGT	4703
rs539577289	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151621786	AAAAATTTTGACTGA[C/T]TCTGTATCCTCTTAA	4703
rs539588988	snp	G/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151493664	GTGGACAAGGAAGAA[G/T]TTTTAAAGATACACA	4703
rs539607744	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151705501	TTAGCACAGCCACCA[C/T]GGAAAACAGTATGGA	4703
rs539611102	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151564510	AGTAAAAGTGACAAC[A/G]AATTTGCACACAGGG	4703
rs539625883	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151732892	ACTTGGTTTTTTGAG[A/C]GCTTAAAGAAAAGCA	4703
rs539629142	snp	G/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151497963	TTTTTTTTCATTTTT[G/T]TGAGTACGGTGCCTC	4703
rs539629438	snp	A/G	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151567052	TCAATTCCCTTTGGG[A/G]ACAAATTAAATATCG	4703
rs539633486	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151663349	TCCCAGCAACAATAG[C/T]AGAAAACAAGACTTT	4703
rs539688897	snp	A/G	0.00119737	0.0244387	intron-variant	NEB, RIF1	GRCh38.p7	2:151513172	TACCAATGAGCATTA[A/G]ACAAGCTAAGATGCC	4703
rs539695426	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151667454	CGTAATTGGCAATTA[A/G]GATTTTAGGAAATAT	4703
rs539695831	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151669308	GTTCCCATTCTACCA[A/G]TATTTATTGGACAGC	4703
rs539701779	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151504919	ATCGCAGCCTGTACC[A/G]CTGCATTTACTAGAT	4703
rs539704700	snp	A/C	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151651273	TCTAACTAGATGCAG[A/C]AATATATGTTTGGTT	4703
rs539727676	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151512594	GCTGGGAATACAGAC[A/G]TGAGCCACTGCACCT	4703
rs539731795	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151636872	GTTGAATTAAGTATA[C/T]ATACATATTACAGGT	4703
rs539735480	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151541221	TCCAAAACACAAGTT[C/T]TATAACACTTAGGAA	4703
rs539739216	snp	A/C	0.00279162	0.0372561	intron-variant	NEB, RIF1	GRCh38.p7	2:151519841	GGGAATAGTAGAAAC[A/C]CAAATGCCAAAGAAT	4703
rs539741763	in-del	-/CTTT	0.0023933	0.0345097	intron-variant	NEB, RIF1	GRCh38.p7	2:151503272	GCTGTTAAGATGTTA[-/CTTT]CTTTAAAAAAGATGG	4703
rs539748914	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151511580	TAAAGCACAGCTAGG[A/G]CACGTTAACTATGGC	4703
rs539752947	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151726667	ATCTAAGGACCAGGG[A/G]CCATTGAGAGCAGTG	4703
rs539763157	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151504214	ATGGCGTGGGGAGCA[A/G]CGTACCCAGATTTTA	4703
rs539764982	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151626529	AATTTGAACCCATAA[C/T]AGCTGTCCCATTCTT	4703
rs539770919	in-del	-/TAAA	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151641296	ATTTCTATGTGTCAT[-/TAAA]TAGTCTTTGCACACA	4703
rs539800267	snp	C/T	0.000215266	0.0103724	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151526009	AGTGTCCCGGGTCTC[C/T]GGTAGTGTTGTGTAT	4703
rs539819851	snp	A/G	2.04635e-05	0.00319865	stop-gained	NEB	GRCh38.p7	2:151562637	TCTCCTGGGCGTTTC[A/G]GACGCGTATAACATT	4703
rs539828580	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151562373	CCCAAGCCTAAAGAA[A/G]CTTGAGAGCAATATC	4703
rs539838130	in-del	-/TTA			intron-variant	NEB	GRCh38.p7	2:151618182	AAGGTATCATAATGC[-/TTA]TTATTATCTTTAAAA	4703
rs539847080	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151561584	TCACTTTTTTTTTTT[G/T]TTGGTTTCGAACACT	4703
rs539856643	snp	A/G	4.97566e-05	0.00498757	missense	NEB	GRCh38.p7	2:151569284	TCACTGAAGATGTCC[A/G]CGGCATGTTTGGCAT	4703
rs539862981	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151561948	GGAAGATCCAGCCCC[A/T]GAGCAGGACACTAGA	4703
rs539868308	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151568244	GGGTAAGTTGTGTGC[A/C]TAATTATCCTACAGT	4703
rs539902145	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151518058	TGGAGTTACCATGAG[A/G]GGTTTGTCCCCTCAT	4703
rs539904520	snp	A/G	0	0	intron-variant	NEB	GRCh38.p7	2:151575393	CTGAGTCTATCGTTA[A/G]TTCTCTTTTCTTGTT	4703
rs539906629	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151707286	CACATGGTCCTTGCC[C/T]TCAAAGAGAGAGATA	4703
rs539921062	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151490312	TCAAAGCATCTCTTA[C/T]AGTAACCATCAATGA	4703
rs539930008	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151517864	ACAGGTGGTCTGCTG[C/T]TGACCAAAAACATCA	4703
rs539930335	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151734082	AGAACAGGATAAATA[C/T]AGGAACGTAGAGCAG	4703
rs539939678	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151525841	AGATTCACATGTAGA[C/T]ATTGATGGTAAGAGT	4703
rs539979338	snp	A/T	0.00358779	0.0422022	intron-variant	NEB	GRCh38.p7	2:151689798	GTGTTTAGCTGTTCT[A/T]TATTGGGACACAAAA	4703
rs539999470	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151713043	CCAATTCCAAGCTCT[A/G]GGACACCTTCTCTGG	4703
rs540029025	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151555695	AAAACTCAGCGATTT[A/G]CACCTCTGTAACAAA	4703
rs540035985	snp	C/G	0.00059943	0.0173019	intron-variant	NEB	GRCh38.p7	2:151548282	TGAAACTCAATATGT[C/G]TCTTGGAGAATCAGC	4703
rs540099871	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151711851	GAAAGAAACTCTGTA[A/C]GAAAGAAAATTGTAT	4703
rs540103059	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151620365	TATATATATATATAT[A/G]TATATATATATATAT	4703
rs540111651	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151726439	AGTATGTATTGCTCA[A/G]CCTCAATAGGATGCT	4703
rs540121903	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151719771	GTAGTCCCAGCTACT[C/T]GGGAGGCTGAAGTGA	4703
rs540140967	snp	C/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151628319	CCCAAATCCAGCTCT[C/G]CTGGGGCACTTGACT	4703
rs540146839	snp	C/T	0.00358779	0.0422022	intron-variant	NEB	GRCh38.p7	2:151631956	AAAACACAGTTAAAA[C/T]ATAACAGTGCTGTAG	4703
rs540147997	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151719520	ATGGACATCAAATCA[A/G]TTGGGATACAAAAGA	4703
rs540154305	in-del	-/T			intron-variant	NEB	GRCh38.p7	2:151629886	ACCTATTATATATCA[-/T]TATAGATTAATATGC	4703
rs540173575	snp	A/G	0.00119737	0.0244387	intron-variant	NEB, RIF1	GRCh38.p7	2:151510485	TTAAGTATTCAGTAC[A/G]GTAGTCCCCACTTAT	4703
rs540200461	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151641733	TACTTCCCATATTTT[C/G]GAAATAAAGAAAAAA	4703
rs540205453	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151674167	TTGAATTTAATGTGG[C/T]AATGTCAGTCAGGGT	4703
rs540221964	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151651366	ATGGAAATGATAATC[C/T]TTACGGGCTAAATGG	4703
rs540227599	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151553236	AATAAGAATGCCATA[C/T]GCCTTCCTGAGAGAT	4703
rs540231493	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151649010	AGTCCTGTCCCAGAA[C/T]GTGTATATCGATAAA	4703
rs540262689	snp	G/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151508599	AGCAGGTGCGGTCAG[G/T]GCTCCCAGCTATAGG	4703
rs540306408	snp	C/T	0.000285118	0.0119364	intron-variant	NEB, RIF1	GRCh38.p7	2:151516581	GGTGATAGAAAGCCA[C/T]GTTAGATATCTCTCC	4703
rs540319303	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151560386	TCTTTGCAAGTGCTT[A/G]TGATTCTCTCCAGGC	4703
rs540324874	snp	A/G	1.65625e-05	0.00287766	missense	NEB	GRCh38.p7	2:151680788	GGAGCATCTTCAATC[A/G]AGGTAAACTTGAGGG	4703
rs540344197	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151681067	TGCTCTCAGGAACCA[C/G]ACAGACTCCTTTCTT	4703
rs540345056	snp	C/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151516049	TTGATTATCTGGGGT[C/G]TTGATAAACATCTTG	4703
rs540352878	snp	G/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151530806	TCTGCCAGCAACATG[G/T]GGAGCAGGACTGTTC	4703
rs540361862	snp	C/T	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151673542	TTGTGTGCAGACCTC[C/T]GAGGAAGATGTTTTC	4703
rs540368653	snp	G/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151509106	TCTCTATGTACTTTG[G/T]TAATATAGGAATTAC	4703
rs540384749	snp	G/T	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151704662	TTTGAGTCGGAAAGG[G/T]AACTCTCTGACCCCT	4703
rs540388719	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151541332	GTGTTAATGGGCATG[A/C]GGTTGCAGCCAGGAC	4703
rs540390514	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151510996	AAATACTGATCTGAA[C/T]TGGGGAGGAACTAAC	4703
rs540401629	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151676019	GGTATTAGAAATATA[A/T]TACTTAGTTCCTAAA	4703
rs540406132	snp	C/T	7.62224e-05	0.00617296	intron-variant	NEB	GRCh38.p7	2:151668995	AAGGAGAGGCCCGCA[C/T]ACGCAATATTAGCAC	4703
rs540412767	in-del	-/ATC	0.00478085	0.0486577	intron-variant	NEB	GRCh38.p7	2:151687083	GACAGTTTGAAAATT[-/ATC]ATTTTAAAAATTGTT	4703
rs540438521	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151669555	AACTTGGAGAGAGGG[A/G]CAGAGGAAGAGCATT	4703
rs540454943	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151504577	CCTGCAAGAGAAATA[C/T]CAAGTATCCTAAAGA	4703
rs540471929	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151537584	TTCATGAAGTTGTCA[C/T]TTCATTGGATCAAAA	4703
rs540483472	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151562031	ACAGCAACTTTCTTT[A/G]CCTGCCCATCAGCCC	4703
rs540494419	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151486341	TGATGATAAAAAAGA[C/T]AGACAATAACAGACA	4703
rs540510067	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151627989	CCTAAATTCTTATTA[A/G]ACTCTACAGCACTAA	4703
rs540510544	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151657924	TTTCCAGAACTCAGC[C/T]CTTATTATTTCGGTT	4703
rs540510741	snp	C/T	0.206029	0.246103	intron-variant	NEB	GRCh38.p7	2:151584335	GGTTTTGGAAACAGA[C/T]AAGAAAGATGCATGT	4703
rs540516732	snp	C/G			missense	NEB	GRCh38.p7	2:151674550	ACATTGTTGCCCTTG[C/G]CTATTAAGTCATACC	4703
rs540542557	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151691403	TCTGTATCATCATCC[C/T]GTATTAGTTTCCTTA	4703
rs540542570	snp	C/G/T	0.000265171	0.0115116	synonymous-codon	NEB	GRCh38.p7	2:151656279	GGCATCCTTTGCAGC[C/G/T]GTGACACTGAGCATG	4703
rs540544669	snp	A/G	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151704535	GGCGTAGGACCCTCC[A/G]AGCCAGGTGCAGGAT	4703
rs540547156	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151634805	CATTTTGAAAACTGA[C/T]TGTACTTGTAAAACT	4703
rs540564866	snp	A/C	3.32116e-05	0.00407488	intron-variant	NEB	GRCh38.p7	2:151546449	TGTATTTAATCTGAG[A/C]GGCAAACACAGAAAT	4703
rs540574500	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151675507	TAAAAATCATCAAAG[A/G]CATTTTCCTATTTTT	4703
rs540588920	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151626616	ATCTCAGCTCACTAC[A/G]AGCTCCGCCTCTCAG	4703
rs540601499	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151707275	ATAAGAAAGAACACA[C/T]GGTCCTTGCCCTCAA	4703
rs540616698	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151660896	ACATAGGCCGATTGA[A/G]TACTTGAAATGTAGC	4703
rs540635854	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151560750	AAATGCATCTGGTTA[A/G]CTTCTGAGTAGCAGG	4703
rs540724600	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151574506	GATTTTATTTTTAAA[A/G]AATAAGAATGGGTAT	4703
rs540738561	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151724787	GGCCTGTCCAATTTT[C/T]TCCTATAAGACAATG	4703
rs540744014	snp	A/G	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151520583	TCTAAAGAGGATGAT[A/G]GCCAGGTGTGGTGGC	4703
rs540749546	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151640226	AAAGGATTAAAATTC[C/T]TGTCGATAAAGGCAA	4703
rs540766586	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151670840	CCCCATTTTCATCTC[C/T]CTGTTTTTCCCATGT	4703
rs540775836	in-del	-/A	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151705744	TGCTACTCAGCCATG[-/A]AAATGAATGAAATAA	4703
rs540787105	snp	G/T	0.00358779	0.0422022	intron-variant	NEB	GRCh38.p7	2:151698486	AGATGGTATTATTTG[G/T]GCAACATTGTAAATG	4703
rs540812788	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151626986	TGTCTTATTTTCCTA[C/T]AAATTGGGGGCTCAC	4703
rs540816110	snp	C/T	0.00119737	0.0244387	intron-variant	NEB, RIF1	GRCh38.p7	2:151489672	AAAGTGCTGGCATTA[C/T]AGGCATGATTCACTA	4703
rs540836141	snp	C/T	0.000399281	0.0141238	intron-variant, synonymous-codon	NEB, RIF1	GRCh38.p7	2:151533535	CATCTTGGCACTAGA[C/T]TTATATTTTCTCTGT	4703
rs540836366	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151543155	GATCCTTTCATCAAC[C/T]AGAGCTCAGACAAAG	4703
rs540843525	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151655217	TGTTACATTATTTTA[C/T]AAGTTCATAAGTTTC	4703
rs540846983	in-del	-/A	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151618547	GTTACAAAATGGGTT[-/A]TCCTAGAGAAACACA	4703
rs540856259	snp	A/G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151640744	CCTAACTTGCTCTAT[A/G/T]TATTAAAAAAAAAAT	4703
rs540861644	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151611707	AGATTGCAGCTAGCT[C/T]TCAAAAGTGGATTTC	4703
rs540875810	snp	A/G	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151496042	AGAGAGAAGCAAAAG[A/G]ATGTTTTATAGGAAA	4703
rs540877796	snp	A/C	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151488979	TTTTTTAGTTGAGTC[A/C]TTAAGTATTATCATT	4703
rs540879298	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151671646	GGGTGCTGCTAAAAA[A/G]CATTTTGTCACTTTT	4703
rs540879300	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151665034	CACAATAAGAAAAAA[A/T]TTGTTGAATACGGCA	4703
rs540891759	snp	A/C/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151495472	AATGTTTTAGAAGCA[A/C/G]TGTACTCAAGTACTG	4703
rs540894838	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151652310	GGCTCACTAAAGCCT[A/C]AGCCTTCCAAGCTCA	4703
rs540894908	in-del	-/AAAAAAAAA/AAAAAAAAT	0.00597534	0.0543715	intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151507112	AAATCCTGTATCTTT[-/AAAAAAAAA/AAAAAAAAT]AAAAAAAAGTCTATG	4703
rs540906577	snp	G/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151488541	GTCCTAGCTATTCTG[G/T]TGGCTGAGGCTGGAG	4703
rs540908117	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151619096	GCTTTCCCTCTATCT[C/G]CCTACTGCCCTCTGC	4703
rs540911325	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151608976	TTGGCAAAGATTGTA[A/T]GAGAAGCAAGGTGCA	4703
rs540945097	snp	C/G	0.000399281	0.0141238	missense, intron-variant	NEB	GRCh38.p7	2:151618405	CCAGCTCTCTTGGCC[C/G]TAACAACTTCCAAGG	4703
rs540950468	snp	C/T	0.00318978	0.0398085	intron-variant	NEB	GRCh38.p7	2:151697984	GGCAGGAGAATTGCT[C/T]GAACCCGGGAGGCGG	4703
rs540978026	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151622672	CCTTGAATACTTTAC[A/C]ATGTATCTCCTAAGA	4703
rs540984657	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151717286	CTGTAGAGTCTTTGG[A/G]GATCATATGTAAAAA	4703
rs541043625	snp	A/G	8.01057e-05	0.00632823	intron-variant	NEB	GRCh38.p7	2:151549776	AGGTTAAATGACATC[A/G]GGCATCAAGTAACTG	4703
rs541055839	snp	A/G	0.00119737	0.0244387	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151498742	CATAGGGATATTTGG[A/G]TTTTACAAACATTGT	4703
rs541070338	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151714313	TCATAAACCATTGTT[C/T]GCTTTGTGGGCCCAA	4703
rs541074474	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151627306	GATAGTCAAATTTCA[A/T]GTATACGTTCTTCAA	4703
rs541077365	in-del	-/T			intron-variant	NEB	GRCh38.p7	2:151667536	TACATCACATATAGA[-/T]TTTTTTTTTCTTTTT	4703
rs541082708	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151556767	CAATAATAGTGGGAG[A/G]CTTTAACACCTCCTG	4703
rs541088387	snp	A/G	0.000778758	0.0197173	synonymous-codon	NEB	GRCh38.p7	2:151563871	AACAATGGGAATGTA[A/G]CGCTCATCCAGGGTG	4703
rs541091289	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151657123	TCCTTTTGGGGTTGC[A/G]TGTGCAAGTTGGGGG	4703
rs541098098	snp	A/G			upstream-variant-2KB	NEB	GRCh38.p7	2:151735293	AGAAAATAATGCCCT[A/G]TTTGGCAAATCCGAA	4703
rs541098123	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151728811	AAAAGAGAACCTAGT[A/G]AGGAAATTGTACATT	4703
rs541102012	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151613564	TTGTCAGCTATAGAA[A/G]TCTCAAATCTTTTTA	4703
rs541102331	snp	A/C	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151721241	TGCTCATCAAAATTA[A/C]TCCAGATTCTATTTT	4703
rs541126160	snp	C/G/T	0.000141977	0.00842451	synonymous-codon, intron-variant, utr-variant-3-prime	NEB, RIF1	GRCh38.p7	2:151497626	TTCTTGCCAAAGTAC[C/G/T]GAGCTAATATTTTCT	4703
rs541137710	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151556372	TCAGGTAAACTTCAG[C/G]GGTGTGTGTCTGTGT	4703
rs541150975	snp	A/G	0.000299715	0.012238	missense, intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151496984	ACTCTCTCCATCTCA[A/G]GAGTGACAGGTAGAG	4703
rs541179237	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151612716	CCCTACCTCCTCTTA[C/T]GGAAACTGTACTGGG	4703
rs541183630	snp	A/C	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151520044	TAATGCAAAACAAAA[A/C]AAAAAAAAAATGGAA	4703
rs541189135	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151505107	AAGTATGTTATACTA[C/T]TTATATGTTTATATG	4703
rs541193797	in-del	-/G	0.00700467	0.0587645	intron-variant	NEB	GRCh38.p7	2:151610469	GCCACCCTCTGGGTT[-/G]GTTCAGCACAGTGGA	4703
rs541207329	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151651547	TAAAAATAACTAAAT[A/G]TGTTAGATTAGGAAG	4703
rs541227605	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151643036	ACAATACTTTAAAAC[A/C]ACATTAGTACCAAGC	4703
rs541247212	snp	A/G			intron-variant, utr-variant-3-prime, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151497846	TGACAAAATGCCACC[A/G]ACTACTTTAGTGGAA	4703
rs541272208	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151493621	GTAAAATCACTGTGA[C/T]CTCGTGGGGTTGGTT	4703
rs541288131	snp	C/T	1.65773e-05	0.00287895	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151650314	CTTGTTCTTTTCTGC[C/T]TCTAAAGAACCCAAG	4703
rs541294994	snp	A/C	0.00279162	0.0372561	upstream-variant-2KB	NEB	GRCh38.p7	2:151735760	ATTCACATGGTAGTA[A/C]ATAAAATCTAACAGA	4703
rs541298841	snp	C/G	0.000399281	0.0141238	downstream-variant-500B, intron-variant	NEB, RIF1	GRCh38.p7	2:151484987	ACGGCTGTAAAGTTA[C/G]AGGGACTTACCTACC	4703
rs541319152	snp	C/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151518668	AGTAAAAAGTTAAAA[C/G]TGAAAGAAACTATTC	4703
rs541327915	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151577521	CATTCCATTTTTATT[C/G]TTTAATGAACATCTA	4703
rs541352177	snp	A/G	6.71659e-05	0.00579469	intron-variant	NEB, RIF1	GRCh38.p7	2:151526873	TGTACCATGGAAGAT[A/G]GCCCTGAGTGAGGTT	4703
rs541355005	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151615448	AGAGGCAAGCGGGTA[C/G]TGAGAAAAAGCTCTG	4703
rs541360752	snp	A/G	0.0103295	0.0711199	intron-variant	NEB	GRCh38.p7	2:151606259	TCTTAAGTCTTATAT[A/G]AAACTATCATCTGTG	4703
rs541363612	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151642536	GAAATAAATCTTTGA[A/G]CCAAAGCTAAGGCAA	4703
rs541389349	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151532540	GTTTTAAGCAGGACA[A/G]ATACAGAGAGCACCA	4703
rs541400243	snp	G/T	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151676874	TCCTCATCTATTTCA[G/T]CTTTATGCCATCAGC	4703
rs541402862	snp	C/G	0.00636936	0.0560724	intron-variant	NEB	GRCh38.p7	2:151656817	TTAGTGCTAAAGAGG[C/G]CTTTAGTAGGTAAAA	4703
rs541404513	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151556662	AAGAAGAAGAGCTAA[C/T]TATCCTAAATATATA	4703
rs541406987	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151702016	TTAGTGCTATAAATT[C/T]CCCTCTACACACTGC	4703
rs541423786	snp	A/G	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151512634	CTTTTTTATTGGGAA[A/G]AACTGATCTGAAGAA	4703
rs541439171	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151556006	ATCTTGCCTCTATAA[C/T]TTTGTTCATGACTCA	4703
rs541454059	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151605374	CATTAGGTCAAATGA[A/T]CTCCTAAGAGTACTG	4703
rs541476865	snp	A/C	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151563232	GTTGGCCAGGCCAGT[A/C]TCGAACTCCTGACCT	4703
rs541478499	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151613661	CCTCAATGTTGGAGG[A/C]GGGGCCTGGTGGGAG	4703
rs541504956	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151508827	TTTGGCTGGAGAGAC[A/G]TGTCCATATAGAGGC	4703
rs541519836	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151570071	TCAACCCCAAATGCA[G/T]CCCACTCACATCGCT	4703
rs541535489	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151705821	TGAAGTAACTCAGGA[A/G]TGAAAAACCAAATAT	4703
rs541537952	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151623504	TTGAATTAAGGATAC[C/T]GGACTAGTATCTGGA	4703
rs541558723	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151690880	TCTTGGTTATACATG[C/T]GCTAACATAAAAAAT	4703
rs541576803	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151636694	ACTGAGGCAGGAGAA[C/T]TACTTGAACCTGGGA	4703
rs541579503	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151539890	GACACTTATACATTA[C/T]CTTGTTTGGTTTTAT	4703
rs541582490	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151529621	CTGCAACCTCCGCCT[C/T]CCAGGTTCAAGCAAT	4703
rs541588943	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151718367	GCTTGGGGCTCTGTG[C/T]CCAATACTCTATGAC	4703
rs541609396	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	NEB	GRCh38.p7	2:151735127	AAGCTGCTAGGAATA[C/T]AGAACCTCTCTCATA	4703
rs541617483	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151677035	CGCTGCTCATGGACA[C/G]GCAGGCAAACGATAC	4703
rs541618851	snp	C/T			missense, intron-variant	NEB	GRCh38.p7	2:151614281	AGCCACTCACATCAC[C/T]CTGCAGGTCATAGGC	4703
rs541628185	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151542131	GTAGCAACTGAAGCT[C/G]CTCAGTGTTTCATTC	4703
rs541641039	snp	C/T	0.000131473	0.00810675	missense	NEB	GRCh38.p7	2:151664578	CATATCCTTTCTTCT[C/T]TTCCTCTTCCCAGCC	4703
rs541642473	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151563365	GTGACCTTGATGCTT[C/T]TTCCTTTTCTGAACA	4703
rs541666044	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151706849	TCTTTTGCAGCTAAG[A/G]TTTAAAAACACTTTG	4703
rs541672313	snp	C/T	0.000168751	0.00918406	missense	NEB	GRCh38.p7	2:151570239	CCACAGGGCTCTGGA[C/T]CTTGGCCTTCCATTT	4703
rs541710927	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151569752	ATTAAAAAAGCATGT[C/T]TGTGCCTACATCCTG	4703
rs541714415	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151576964	TGTGTGGTAGTGCCC[A/T]TGTGCATTCTAAAAG	4703
rs541725812	snp	A/C	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151721655	GCCTGATTATAAATT[A/C]TAAGAGGAAAGGATG	4703
rs541737756	snp	A/T	1.65616e-05	0.00287759	missense	NEB	GRCh38.p7	2:151697381	GTGACTTTCATGCAG[A/T]GTGAATGGTATGGAT	4703
rs541739087	snp	A/G	0.0023933	0.0345097	intron-variant	NEB, RIF1	GRCh38.p7	2:151526509	TTACGTTCACAGCAC[A/G]CTCAGATATGCCATT	4703
rs541765128	snp	A/G	6.82431e-05	0.00584097	intron-variant	NEB	GRCh38.p7	2:151549605	GCCACCCCACCTTCA[A/G]ACCCATCTCAATGAG	4703
rs541787991	in-del	-/G	0.0023933	0.0345097	intron-variant	NEB, RIF1	GRCh38.p7	2:151504813	CCTGATATTTCAGGT[-/G]TGGGGGACACGTGCC	4703
rs541803243	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151490541	AGATGCAGTTGGGGG[A/G]GATGTAGCAAACATG	4703
rs541803470	snp	C/T	5.02727e-05	0.00501337	missense	NEB	GRCh38.p7	2:151671192	GGGATCCATCCGATG[C/T]CCTTCAAGAAGCTGT	4703
rs541839240	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151721046	CCACCAGTCTACAGT[C/T]AGAAGCTCCTCTAGG	4703
rs541853407	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151721021	CCAGCTGTGCCCCTA[C/T]TCACCCAGACCACCA	4703
rs541879026	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151663433	ACAAATGAAACACTA[C/T]GTTGGGAAATTGCAG	4703
rs541884259	snp	G/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151512149	CATTCTCCTGCCTCA[G/T]CCTCCCAAGTAGCTG	4703
rs541884621	snp	A/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151505314	AAAAGTGGTTTCTTA[A/T]CTACTTTTGCAACCT	4703
rs541908352	snp	A/G	0.000170034	0.00921891	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151496277	TTCTCGCCAAGTACC[A/G]AGCTAATATTTTCTT	4703
rs541920805	snp	A/G	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151503728	AATGAGAAAAATCTA[A/G]CCATTTTGTTGCATC	4703
rs541922943	snp	G/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151519433	AAACAGGCAAATGCA[G/T]AGAGACAAAAAGTAG	4703
rs541937969	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151628616	GAAGCCGAGGGAGGC[A/G]GATCGCCTGAGGTCA	4703
rs541971525	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151526471	CAAAATGGATCTCGT[A/G]ATGAATCTTTATATA	4703
rs541979214	snp	C/G	0.00478085	0.0486577	intron-variant	NEB	GRCh38.p7	2:151619217	AAGCCTGAATCCCTA[C/G]GAAGATTTATACCTG	4703
rs542001695	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151547202	GGTCACTGAGTGATC[A/G]AGAATGATGGCAATT	4703
rs542012620	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151649656	AATATTTATTGAGTA[C/T]CTATTATGTGCTAGA	4703
rs542013157	snp	A/T	0.000399281	0.0141238	missense	NEB	GRCh38.p7	2:151541450	CTCTGAGCTTACCTG[A/T]CTCTGAAGCTTCTGC	4703
rs542029783	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151657452	TTTTTTGCCGGCCAG[C/T]GCAGGGAAAGCCTCA	4703
rs542055948	snp	A/G	0.000186376	0.00965159	intron-variant	NEB	GRCh38.p7	2:151606561	ATAGTCTCCCTGCTC[A/G]TTTTGTAGAAAAGAA	4703
rs542064000	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151611529	GAGCACTCAATTGTA[C/T]TAGCCTAATGATTGG	4703
rs542074583	snp	A/C	0.00438332	0.0466095	intron-variant	NEB	GRCh38.p7	2:151713647	GCAGGTACAGAGAAA[A/C]TAAAGGGACTTTCCA	4703
rs542075875	snp	A/T	0.00478085	0.0486577	intron-variant	NEB	GRCh38.p7	2:151649274	ATCAGCATTATAAAA[A/T]GTCTGTGAGGGGTTA	4703
rs542092706	snp	C/T	0.000182347	0.00954674	missense, intron-variant	NEB	GRCh38.p7	2:151614314	TCCGAGCCTGAATGA[C/T]GTCATTCTGATCAGG	4703
rs542104135	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151682012	CTTGCCATTACTTTT[A/G]ATGTCAAAACTGCAA	4703
rs542106802	snp	C/T	4.98451e-05	0.004992	intron-variant	NEB, RIF1	GRCh38.p7	2:151526144	AGCAGAACTCATGGG[C/T]GGCTGGGGGTTACCT	4703
rs542109967	snp	C/T	0.00119737	0.0244387	intron-variant	NEB, RIF1	GRCh38.p7	2:151491189	GTGTACAACACCACT[C/T]GCGGCTAATTTTTTT	4703
rs542134067	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151498498	GACTCAACCTGTTTG[C/T]TTGAGCCTAAAGACA	4703
rs542149432	snp	G/T	0.000887813	0.0210504	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151531801	ACTTACATCGCTGAT[G/T]TGTTTGTTGACTTTT	4703
rs542174363	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151539855	ATTTTCTGAGTAACT[A/G]GGAGCCCAGCAGCAT	4703
rs542201618	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151509243	AAAGCCAGATTTTTC[A/G]GAAGAAACGGTAGTT	4703
rs542238394	snp	A/C/T	0.00318978	0.0398085	intron-variant	NEB	GRCh38.p7	2:151653225	ATTTATTCACTATAA[A/C/T]CAAGACCTTCTGAAT	4703
rs542245348	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151659717	GGTAGCATTTGCCTC[A/C]TAAAATTTTCTGTGT	4703
rs542263096	snp	C/G	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151494458	CACCTGCCCTGAAAC[C/G]CTTGAGGACTGCAAG	4703
rs542275170	snp	C/G	0.000399281	0.0141238	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151493798	AGTTTTCTTGATTGC[C/G]TTTCACTCTTTCCAT	4703
rs542285056	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151712465	GTAAGATCACTCAAC[C/T]CCCTCATCCAAAGTC	4703
rs542285125	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151705073	ATTTTTTTAAACAAA[A/C]CTTCATGAAAAAGTT	4703
rs542325814	snp	G/T			utr-variant-3-prime, intron-variant	NEB, RIF1	GRCh38.p7	2:151485752	ACAAGTGTGATGCTT[G/T]GAAATGCCTAAATAG	4703
rs542330320	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151624996	AGCTCAAGTTATTTT[C/G]AGCACATTAAATACA	4703
rs542338580	snp	A/C	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151500403	AGGTCTTGATATAGA[A/C]GCTTCAGAGTTGTAT	4703
rs542367734	snp	C/T	0.00358779	0.0422022	intron-variant	NEB	GRCh38.p7	2:151690172	TGAGAAGCACTGCTG[C/T]TTTCCCCCGATCTTG	4703
rs542377970	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151642451	TTTTAAACCATTCAT[C/T]GAAACAATAAACTGT	4703
rs542392215	snp	A/T	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151684389	ATGTAAAAATCATTG[A/T]TAATGATGAATGTGA	4703
rs542407202	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151665950	ACCTATAGTTCAAAT[A/G]AGTGAAATCCTAAAA	4703
rs542410070	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151646494	ATCTAGGTAATTACA[C/T]GCCTTGCCAATATTA	4703
rs542423499	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151639538	CGGGTAATAAGTTCA[C/T]AAAGGAATGTGTATT	4703
rs542423844	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151648495	ACAAGAGCAATTGCA[C/T]TGTGGTGAAGTCAGG	4703
rs542456282	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151566944	AGCAGCAGATTTTTT[A/T]TAAAAAAATTTGATT	4703
rs542457486	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151721318	TTACCGTTCCATGTC[A/G]AAGCAATTTTGTCTG	4703
rs542473152	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151533890	TTTTGTTTGTTTTTT[A/G]TTGTTGTTTGTTTAT	4703
rs542473359	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151645819	GATAAGCACTGTAGA[G/T]TCAATAAGAATTGCC	4703
rs542515750	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151605337	GATAATCTCCATCAC[C/T]AAGCTTCCCTGACAA	4703
rs542519903	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151705598	CAAAGGAAAAGAAAT[A/G]ATATGAAAAAGACAC	4703
rs542531221	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151696576	TCATTGGATTTTATG[C/T]ATAGAGTTATGAAAT	4703
rs542546078	snp	A/C/G	0.000220747	0.0105037	intron-variant	NEB	GRCh38.p7	2:151548456	TCAATGATGGGTAAA[A/C/G]AAGGACCAACATTAC	4703
rs542552121	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151601345	AACTCCTGACCTCAA[A/G]TGATCCACCCGCCTT	4703
rs542576990	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151693593	CCTGCAAAGGACATG[A/G]TCTGATTCCATTTTA	4703
rs542585539	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151529004	ATGGCATGGGATGAA[A/G]CTTCCTTTGCTCTTC	4703
rs542606113	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151519825	ATCAATTTGGGAATT[A/G]GGGAATAGTAGAAAC	4703
rs542610724	snp	C/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151572248	CATCGCTTGAACCCG[C/G]GAGGCAGAAGTTTCA	4703
rs542627829	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151660218	TGGCCAAGACTTTGT[C/G]ATGCCAGCATCACTG	4703
rs542631751	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151494857	GTTTCACTATGTTGG[C/T]CTTGCTGGTCTTGAA	4703
rs542645206	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151544312	TTTACTCTGAAGCAC[C/T]ATAAGTTACCAATTG	4703
rs542647964	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151571258	TGATCCACCTGCCTC[A/G]GCCTCCCAAAGTGCT	4703
rs542686767	snp	A/G	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151578057	TGGCAATGCATTTTA[A/G]GTGATGAGCATGCTT	4703
rs542692600	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151697943	TGGTGGCGGGTGCCT[A/G]TAATCCCAGCTACTT	4703
rs542706227	snp	A/G	6.63306e-05	0.00575855	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151485924	AGTCATACATGGCAC[A/G]GAAGATTTTCTATTC	4703
rs542721837	snp	A/C	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151616497	AGTTTGAGAAGAGAC[A/C]AGCCTGGCCAACATG	4703
rs542729527	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151698357	AAAACATTTCATCAT[C/T]TCAAAAAAGCAAAAC	4703
rs542731924	snp	A/G	0.00119737	0.0244387	intron-variant	NEB, RIF1	GRCh38.p7	2:151508176	CCAATGGGACCTAAA[A/G]TAGGCTATTTTAGCC	4703
rs542763719	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151708551	CAGAGCTCAGCCCCT[A/G]AAGTTTTCTGTTTAC	4703
rs542765197	snp	C/T	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151607216	AAAGTCCTGGATCAA[C/T]TAAAAAAACCTAAGA	4703
rs542768248	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151631474	AGCGCGTTGTATAAG[G/T]CAAACTAAAAGAATT	4703
rs542782332	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151543534	TAGTCCAACTCTTCA[C/G]TTTAGGAAATTAGGG	4703
rs542782355	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151551937	CTGCTTCCCTTTGCC[G/T]GGAGAACTCATCTGA	4703
rs542810745	snp	A/G	0.00478085	0.0486577	intron-variant	NEB	GRCh38.p7	2:151675170	TATGGGATATGTTCC[A/G]GTAGGGGATTTGTGA	4703
rs542822883	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151663158	TGGTAGAATGAAACC[C/T]GGTTGGGAGGGAGGG	4703
rs542860663	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151488191	CTTTATTCTTTTTCA[A/G]TATTAATATTTTTGT	4703
rs542880080	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151573798	AAATGGTATCTTCCT[C/T]GAACTTTCTTGAATT	4703
rs542880285	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151731365	TTAAGTTAGAGTAGA[A/G]AGAACAGTAAAACTT	4703
rs542886788	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151729903	AGAAAAATGTATGAG[G/T]CTGTTTTTTAATCAA	4703
rs542895768	snp	C/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151529443	CGGAATTTTAAAAAT[C/T]TGCTGTGGAGCAAGG	4703
rs542898222	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151722902	ACACAGAAAAAGGGA[A/G]ACACACCACAATTTG	4703
rs542901451	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151693050	GTGAACCTTAGATAA[C/T]TAAGCACAGTCCTGG	4703
rs542910032	snp	A/T			upstream-variant-2KB	NEB	GRCh38.p7	2:151736008	AAATGAGCATTGACC[A/T]TCTTAGTCATTTTTA	4703
rs542916866	snp	A/G	0.0251073	0.109194	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151581498	ATTGCTGATCTGCAG[A/G]GCATTGATTTTGGAT	4703
rs542917965	snp	C/T	0.000399281	0.0141238	missense, intron-variant	NEB	GRCh38.p7	2:151610072	CTTCAATGCTCTGGG[C/T]TCCAATGTGGTGGCC	4703
rs542924938	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151702729	TGCTTGGTAGATCTT[C/T]CACCATCCTTTTATT	4703
rs542928634	snp	A/G	0.0023933	0.0345097	intron-variant	NEB, RIF1	GRCh38.p7	2:151514007	CATAACTAAGATTAC[A/G]CTTAGGTGCACACCA	4703
rs542945412	snp	C/T	0.000489788	0.0156414	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151579347	ACTTACGTCGCTCTG[C/T]AGGTCGTAGGCTTTC	4703
rs542945536	snp	C/G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151706715	GTAAGGCACATTGTA[C/G/T]TCAGAGGGACTCATG	4703
rs542948999	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151685955	ACTTGATCTTCCTTC[C/T]CATATTTTGTGGGTG	4703
rs542967158	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151685368	AAAACCATATGACAA[C/T]TGGATTTTAATAAAA	4703
rs542975095	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151637323	GTGCAGAGGAAATCA[C/T]GTGAATCAAGGCACC	4703
rs542981685	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151607450	ATAACACTCTCCATG[A/G]GCAGACAGATATTGC	4703
rs542982049	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151637776	CTATATTATAGGTTT[A/G]GCTAATAATTCAGTC	4703
rs542983606	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151689809	TTCTTTATTGGGACA[C/T]AAAATATTAAGATGC	4703
rs542996647	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151521120	AAGATGAAAGACTCA[C/T]TAACACCAGTACCCC	4703
rs543012140	snp	C/T	4.96816e-05	0.00498381	missense, intron-variant	NEB	GRCh38.p7	2:151644005	TTCTCAAAGTCCTTC[C/T]TGTACTCCCTGTCAC	4703
rs543032074	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151665797	AATGAAAAATTAACA[C/G]AATTTTGCACTGGAA	4703
rs543037801	snp	G/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151652087	TGGAAGTGGAAATAG[G/T]CTGCTTTGTGGTGTT	4703
rs543071934	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151551303	CAAGATGGGAAATAA[C/T]ATGAAAAGTTGAGAC	4703
rs543100735	snp	A/T	0.000248379	0.0111413	missense, intron-variant	NEB	GRCh38.p7	2:151633716	GGTCAGGCAGGCATG[A/T]CCACTCGTGCAGGTA	4703
rs543102903	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151651503	AACCTTGTCCTGTTT[A/G]GGATCTATATCTTGC	4703
rs543114788	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151722327	AGGCCCAAGTGGGTC[C/T]CTCTGCTGCTGTTGC	4703
rs543122492	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	NEB, RIF1	GRCh38.p7	2:151485410	TTCAGAACTGAATTA[G/T]AAATAATAAGCATTA	4703
rs543126725	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151691593	TAAATAATGAACACT[C/T]ATCTTAAATCTGCAT	4703
rs543131351	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151527458	GTATGCAGTTACAAT[C/T]GTCTGTGTCTCTCCT	4703
rs543138263	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151623649	GTCTTTTCAAGATGA[G/T]ATTTTATAAGAAAAA	4703
rs543192540	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151672122	CAAAGTGGCTCTCAT[A/C]GTTAGTGGAATATAG	4703
rs543212623	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151672304	TAGTATGAAGTCTAA[C/T]AAAAGCGAGAAGTGA	4703
rs543214700	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151692872	CTACTTGGGAGGCTG[A/G]GGCAGGAGAATTGCT	4703
rs543217471	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151665231	CACCGGCACGAAGAC[A/G]ATCAGAAAGAAACAC	4703
rs543223920	snp	A/C	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151528293	TAGGCACATTTCTTT[A/C]CTCATTCTTTCTCTC	4703
rs543224168	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151534960	TATTTTCATTTTTAG[A/C]AATATTGTACTAATT	4703
rs543243569	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151653109	CCATTTTTAGGCATT[A/C]CTTTCCTGCACTCTG	4703
rs543247547	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151573044	CATGAGTCACTTTAA[C/T]GTGAATTTGCTTTGT	4703
rs543252190	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151715691	TTAGACTCCCAGCCT[A/C]CAGAACTGTGAGAAA	4703
rs543269236	snp	C/G	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151659516	ATGTTGCCCAGGCTG[C/G]TTTCAAACTCCTGAG	4703
rs543345499	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151523162	ACATCTCATTACTCT[C/T]AGAGATTCCACTGTT	4703
rs543356769	snp	A/C	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151521699	TTTCAAGCAGCAATC[A/C]CATTGATTCCACTTC	4703
rs543366982	in-del	-/AACA	0.00755907	0.0610114	intron-variant	NEB, RIF1	GRCh38.p7	2:151509158	AATCTTGCCAGAGAC[-/AACA]AACAAACAAGCAGTT	4703
rs543373554	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151678902	ACATTTGTTATTCAA[C/T]CATCACATATTTACA	4703
rs543415168	snp	C/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151697865	AGGTCAGGAGTTTGA[C/G]ACAAGCCTAGCCAAC	4703
rs543424623	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151679528	ATTAGAACTGATCAG[C/T]AGAAGGTTATACAAA	4703
rs543428309	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151628352	CTGAAGTGGTCTGGA[A/T]TATATTCCCATACTA	4703
rs543452660	snp	A/G	0.000798403	0.0199641	downstream-variant-500B, intron-variant	NEB, RIF1	GRCh38.p7	2:151485096	GCCATCCTACTGGAT[A/G]CAGATGGGAAAGATG	4703
rs543463673	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151550534	GGATGCATGTGTTCA[C/T]GGCAGAAAGGGAGGA	4703
rs543480189	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151529748	TGGCCAGGCTGGTCT[C/T]GAACTCGTGACCTCA	4703
rs543481312	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151606486	AATACAGAAAGCTTC[C/T]AGCACAGGATGAGAT	4703
rs543483258	in-del	-/A	0.308661	0.24302	intron-variant	NEB	GRCh38.p7	2:151572872	TATATATTTTTAACT[-/A]AAAAAAAAAAAAAAA	4703
rs543484495	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151716207	GTAATGGCACAATCT[C/T]GGCTCACTGCAACCT	4703
rs543484501	snp	A/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151707873	ATCAACCCCTCAGCC[A/T]CCACAGAGCATCACG	4703
rs543499102	in-del	-/AAAG	0.0130921	0.0798413	intron-variant	NEB, RIF1	GRCh38.p7	2:151508528	GGAGGGTTAAGAGTC[-/AAAG]AAAGACATGACCTCT	4703
rs543499208	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151558530	AAGCTGGAGGCATTA[C/T]GCTATCTGACTTCAA	4703
rs543506644	snp	C/T	0.000399281	0.0141238	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151492115	GTAATAGTCTCCTGA[C/T]CTTGGTCATTCCGTT	4703
rs543524715	snp	A/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151513955	TTCTCTGCTTAGAAG[A/T]TTAGAGTATAAAGTA	4703
rs543550263	snp	C/T	0.00557542	0.0525036	intron-variant	NEB	GRCh38.p7	2:151678690	AGGAGGGGGTAAACA[C/T]TAACTGGCTCTGGAT	4703
rs543560458	in-del	-/TCATATAATC	0.00159617	0.0282053	intron-variant	NEB, RIF1	GRCh38.p7	2:151519877	TTGTACATAGAGTGA[-/TCATATAATC]TATTATCCAAACTGG	4703
rs543570092	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151498426	GCTTTGGAGCAGTTG[A/G]GAGTGGGAAGGGAGG	4703
rs543571584	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151548085	ATTTCTTTAGAAAAG[C/T]TTTGCATCATAATCT	4703
rs543576274	in-del	-/AA			intron-variant	NEB, RIF1	GRCh38.p7	2:151532970	TTCAGCATCAAAGTC[-/AA]GAGGCGCCATGAATA	4703
rs543596736	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151541375	GAGTCTGCCACTGGC[C/T]AGGTGAGGCCAGGCA	4703
rs543627504	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151634268	AGAGAACATTTGAAC[A/C]AGGGAACCTGTAGAA	4703
rs543644491	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151487175	GAAGAATTTGAAAAC[C/T]CGTAGCACTATTGCA	4703
rs543655045	snp	A/T	0.0023933	0.0345097	intron-variant	NEB, RIF1	GRCh38.p7	2:151494388	GGTTAGATGGAAAGT[A/T]GTATGTTTCCTAAGG	4703
rs543664411	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	NEB	GRCh38.p7	2:151735940	TTGTTGAATTAAAAA[A/T]TAATACAGGCCCATA	4703
rs543688476	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151713540	AAAGATTAGTTTTTT[A/T]AAAAAAATTTAGGCT	4703
rs543690192	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151524143	TCTAGACAGCTTAGA[A/G]GGAAACGAGAAAAGG	4703
rs543709356	snp	G/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151616963	AATGCCTGGAAAAAT[G/T]TTAACATCAAATGAT	4703
rs543712234	snp	C/G	0.00279162	0.0372561	intron-variant	NEB	GRCh38.p7	2:151578790	GAAGGAAGGAAGGAA[C/G]GGCGGGCAAGGCTGG	4703
rs543713432	snp	C/G/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151704634	TTTTCCAGGTGCGTC[C/G/T]GTCACCCCTTTCTTT	4703
rs543755429	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151520874	GTCTCACAAAATAAA[C/T]AAGAGGATTTATTTA	4703
rs543770578	snp	C/T	1.65704e-05	0.00287836	missense, intron-variant	NEB	GRCh38.p7	2:151643151	AACATAGGACTTACA[C/T]GATTCATGGTAATAG	4703
rs543795912	snp	C/T	1.65589e-05	0.00287736	missense, intron-variant	NEB	GRCh38.p7	2:151643907	GGTAGTTCTTGTAGT[C/T]CACGTCGCTGACTAA	4703
rs543800943	snp	C/G	0.00755907	0.0610114	intron-variant	NEB	GRCh38.p7	2:151690975	CTTCTCTGTCTGTCT[C/G]TCTCTCTCTCTCTCT	4703
rs543808992	snp	G/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151533316	ACAAGGAATGAATAT[G/T]TACATAGCTTTACCA	4703
rs543827269	snp	A/T	0.000645709	0.0179565	missense	NEB	GRCh38.p7	2:151657994	TTACATCACTTGCAA[A/T]ATCTCTGGAAGCCTT	4703
rs543830856	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151577554	TCTCGGTTATCAATG[G/T]GAACTCCCTAAAGTC	4703
rs543833425	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151610209	ATGAAATGGACAAGA[C/T]TTTATATTACAAACA	4703
rs543836428	snp	C/G	9.20175e-05	0.00678235	missense, intron-variant	NEB	GRCh38.p7	2:151592062	AGAGCATTGATTTTG[C/G]ATTGCAGCATCAGGG	4703
rs543850875	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151532660	AGGTTAAGCTCTTAA[C/T]TGGAGCTTAACCTCC	4703
rs543858018	in-del	-/AACAA	0.000401526	0.0141634	intron-variant	NEB	GRCh38.p7	2:151616699	CTATGTCTCAAACGT[-/AACAA]AACAAAACAAAACAA	4703
rs543874057	snp	C/G	0.0240643	0.107019	intron-variant	NEB	GRCh38.p7	2:151583990	AGATGGTATGGTGAA[C/G]AAGAGTAATGAAAAC	4703
rs543882211	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151704500	CAGACTGCTGTGCTA[G/T]CAATCAGCGAGACTC	4703
rs543891880	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151657169	CCAAATTACTCCAGC[A/G]TAATAGAGGGGAGAA	4703
rs543917506	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151704648	CCGTCACCCCTTTCT[C/T]TGAGTCGGAAAGGTA	4703
rs543954741	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151636765	CAGCCTGGGCAACAA[G/T]AGTGAAACTCCATCT	4703
rs543961404	snp	C/T	0.000862627	0.0207502	synonymous-codon	NEB	GRCh38.p7	2:151678044	GTTGTATTTGGACTT[C/T]GTCTTCTCATAGTCT	4703
rs543983879	in-del	-/TTTTG	0.00438332	0.0466095	intron-variant	NEB	GRCh38.p7	2:151641324	ACACATGACTGTTTT[-/TTTTG]TTTTGTTTTGTTTTG	4703
rs543990700	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151733576	AGCTGAAATTTATCC[C/T]CCAGCACCAAAATTC	4703
rs543995438	snp	A/G	0.00358779	0.0422022	intron-variant	NEB	GRCh38.p7	2:151685767	CTCACCAATTACTTT[A/G]ACAGAAAAATGTTGA	4703
rs544004969	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151710133	CCTCAGGCAAAGAAT[A/G]ATTAAAAAGAGTCCC	4703
rs544026234	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151557645	GCAAACCAAATCCAG[A/C]AGCACATCAAAAAGC	4703
rs544053490	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151732852	AGCAGTTTTAGAAGA[C/T]GAATTAAAACCTGCC	4703
rs544057137	snp	A/G	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151561993	GAGAGGAGGGGCTTT[A/G]GTCAGTTAGAGCCTA	4703
rs544060798	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151564019	AATTAAGGTGAAACA[C/T]GTATGTTCAAGGCAA	4703
rs544069233	snp	C/T	0.000298201	0.012207	missense	NEB	GRCh38.p7	2:151725533	ATGGCTGTCCTTTTG[C/T]TTTCTCAAACTTCTC	4703
rs544083672	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151668340	TCCAGATGTAGTACA[A/C]CTCAGCTTTAATTGA	4703
rs544106474	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151718752	TTAGCTCCTTCCCTT[C/T]AGCCTATAAAAGACT	4703
rs544154834	snp	C/T	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151694949	TACTTTTTTATGATA[C/T]AAAGGCATCACTTTC	4703
rs544182833	snp	C/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151638992	GGAGATACATGTATA[C/G]GTCAATTGCTAATAT	4703
rs544184007	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151566499	TTAATGATGAGAAGA[C/G]CCAGGGAGCATTAGC	4703
rs544200886	snp	C/G	0.000182157	0.00954176	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151524548	TGCCTGTGTGGCCTT[C/G]TTGATGTCTGGTCGA	4703
rs544217482	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151516746	TAGGTGTTGAGGGGA[C/T]GGGTACCATTACTGT	4703
rs544220811	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151622889	AGAATGAGTAGCATT[C/T]AGTTCTCTAGTTTAT	4703
rs544225993	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151648024	AATTTCTCATATAGA[C/T]ATATAGATATAGATC	4703
rs544243498	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151613687	GGGAGGTGATTGGAC[A/T]TCCCCCTTGCTGTTC	4703
rs544280263	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151654441	TTTTGAAGATAGATA[G/T]TAAGATAATTGCTAA	4703
rs544282408	snp	C/T			synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151619748	CTGTTTACGATATGC[C/T]TCTTTGTATTTGTAC	4703
rs544291371	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151673483	TTATACTGTAGACTT[C/T]CACTTTCTACTTAGA	4703
rs544299391	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151686888	CAAAATTCAGGCAAA[A/G]GGCATGAAAAGAAAT	4703
rs544311834	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151724088	TGCCTAGGAGCTTTC[C/T]TCTCAGTTCCTTTTT	4703
rs544334101	snp	A/G	1.65669e-05	0.00287805	missense	NEB	GRCh38.p7	2:151679971	ACTGGGGCAGGTCTG[A/G]TGGCAGGTTGTATTT	4703
rs544335030	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151566020	TTGGTGTTTTGATGA[A/G]TAAGTATAAAGAAGG	4703
rs544336075	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151687350	GAAATTCTTTTCCAC[A/G]CTACTACCCTTGGGC	4703
rs544340668	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151537449	CATTTTTAATACTAA[C/T]TAAAGCAATTCAAAT	4703
rs544356078	snp	A/G	0.00279162	0.0372561	intron-variant	NEB, RIF1	GRCh38.p7	2:151510344	AGGAAAGGCCTAGCC[A/G]AAACTTTTGGTGGGC	4703
rs544356647	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151516854	CTGATGCAAGAAAAC[A/G]CATGGGGAAAATTAC	4703
rs544392853	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151683147	CAAATTAAAATAGAA[A/G]GCCACATTGAAGGTG	4703
rs544394354	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151674924	ATGTCAAGAGAAGAC[C/T]TGGTGGTCAGCTTTA	4703
rs544396827	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151576457	GTATATATTATATAT[A/G]CAACATAAAATATAT	4703
rs544398473	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151554321	ATCCCAGCACTATGG[A/G]AGACTGAGGCAGGAG	4703
rs544442915	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151709965	ACAATTAAAATAGGC[C/T]AAAAACAGAATTAGA	4703
rs544453966	snp	A/G	0.000143536	0.00847039	synonymous-codon	NEB	GRCh38.p7	2:151568083	TACCTCACTCTGAAC[A/G]TCATTGCAGTGATGG	4703
rs544471446	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151717283	TTGCTGTAGAGTCTT[C/T]GGGGATCATATGTAA	4703
rs544492715	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151688599	TTGTCCTTGGGGGAT[A/G]CTTTTCAAGACCCCC	4703
rs544494923	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151517332	ATCTCCGAGCTCTTG[A/G]GTTGTAACAAGATGT	4703
rs544521035	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151706074	AATGACTGAAATAAA[A/G]TGTTTTTTAAAAGAA	4703
rs544525796	snp	A/G			missense	NEB	GRCh38.p7	2:151569342	TCCACCCAATTCCAC[A/G]CAACCATTCCAAGTC	4703
rs544527677	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151640899	TTAATACATTCTTTA[A/G]TGTGAAAGTCATTCT	4703
rs544575376	snp	C/T	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151632315	ATTTTGTAGTCTAGA[C/T]AAAAAAAAAAAAACT	4703
rs544587883	snp	C/T	0.00119737	0.0244387	intron-variant	NEB, RIF1	GRCh38.p7	2:151488827	TTACCCCTTTCTTGC[C/T]GATTTATAATTCTTT	4703
rs544598491	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151661198	TGATTCTCCTCTTGG[C/T]ATCATTATCCTGAAA	4703
rs544605837	snp	A/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151731291	AATCTCACTCTTTTT[A/T]TAGAGCTGTGCCACT	4703
rs544625291	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151666864	ACCATGTCTGGTCAA[C/T]GTATGCTTTTTTATG	4703
rs544647168	snp	C/T	0.000139066	0.00833748	intron-variant	NEB	GRCh38.p7	2:151610880	TGCTACAGGGCAGGG[C/T]GGCATGGGGCATGGG	4703
rs544666336	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151653825	GCCCTTTTGACATAT[A/G]AACAGTGAAAGAGAA	4703
rs544684151	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151610201	CAGACAACATGAAAT[A/G]GACAAGATTTTATAT	4703
rs544693073	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151693477	TGTATCCATGTGTTC[C/T]CAACATTCAACTCCC	4703
rs544714293	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151631699	CAGGCCCTTAGTGAA[G/T]CAATTTTAGGCCGAG	4703
rs544719028	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151609678	TATTAAACAATGTGA[A/G]TGGTACCCCCAGCCC	4703
rs544731220	in-del	-/A	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151613140	AAAAGTGCTTGATTT[-/A]AACCAGAGCTTGATT	4703
rs544731507	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151660248	GTTCAACTTCTCCTC[C/T]GGCCTAGTCCTTCTT	4703
rs544760870	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151516732	TTTTTGTTGTTGTCT[A/G]GGTGTTGAGGGGATG	4703
rs544761884	snp	A/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151709162	CCTGCGACCAGGTTT[A/T]TTCATAGTCAGTGGG	4703
rs544767693	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151519603	TTGCACACTTAAAAA[C/T]AGTTAAAATGGCAAA	4703
rs544771331	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151667614	CTCACTGCAGCTTCA[A/T]ACTCCTGGGTTAAAG	4703
rs544775500	snp	A/G	1.69378e-05	0.00291009	intron-variant	NEB	GRCh38.p7	2:151546333	TTATGCATTGTGATG[A/G]TGTGCACTCACCCAG	4703
rs544799431	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151702848	TGTGCCTTTTAATTG[A/G]AGCATTAAGTCCATT	4703
rs544802320	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151660313	CTCCAATTTTCATCT[C/T]AGCGTCTCCTTTCAG	4703
rs544836440	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151660851	AATGATGGAAATGTT[C/T]TGCATAATCCAATAT	4703
rs544837067	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151633573	AATCTTAACTTGAGT[A/G]ATGGATTGTATATAA	4703
rs544840737	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151681699	TCTGCCCTCCTTGAG[A/G]ATGTACTCACCTGAC	4703
rs544910782	snp	A/C	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151502256	GGAATAAAACACTAC[A/C]AATATGGTGCAGTGT	4703
rs544923426	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151508958	CATCGCTTGTCACTG[C/T]CCTTTCACTTTTCTC	4703
rs544950658	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151704437	ATCAAGCCTGGGCAA[C/T]GGCGGGCGCCCCTCC	4703
rs544978867	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151573848	TGGATTATCTTGTAC[C/T]CACAAATAGTTTTTT	4703
rs545007307	snp	A/C	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151523780	GTGCATACCCTGATC[A/C]AACACTTGCCAAACA	4703
rs545014209	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151654419	TTAATACCGCCTGGG[C/T]TTACTATTTTGAAGA	4703
rs545028504	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151572882	TAACTAAAAAAAAAA[A/T]AAAAAAGCCCGGGGC	4703
rs545030782	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151536346	CAAATAGATTTATTT[A/T]CCATATTGGGCAAAA	4703
rs545034738	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151565330	TATCTAAAAGTGAAT[A/G]CAATTCACCACCTGC	4703
rs545048178	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151494847	TAGAGACGGGGTTTC[A/G]CTATGTTGGTCTTGC	4703
rs545059735	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151665145	TAACATGCTGTTGAG[A/C]GATGATCTGAGGGGT	4703
rs545065178	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151572373	TACAAAATAGTTAAT[A/G]CAAACGTGTATTATG	4703
rs545085837	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151569685	TGTACACAAAAATTT[A/T]TGGATTTTAAAATCT	4703
rs545091147	snp	A/G	1.66255e-05	0.00288314	synonymous-codon	NEB	GRCh38.p7	2:151692303	AAGTTGATATTTTGG[A/G]GTCTCACAGTAATTC	4703
rs545099391	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151551378	GCAGGTGGGATCCAG[C/G]TTCTTTCTCTTCTGA	4703
rs545106602	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151730556	ACAGAAGGAGAGGCT[C/T]GTTTAGGCCAAGCAC	4703
rs545107350	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151502208	ATACAGTGAACTTTG[A/G]GGACTTGCAGGAAAG	4703
rs545111131	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151709877	ACCCTGTCCTTGGTT[C/T]AGGCTGGTCAGATTA	4703
rs545121121	snp	A/G	0.00358779	0.0422022	intron-variant	NEB	GRCh38.p7	2:151666883	TGCTTTTTTATGACT[A/G]TATTTCCATTATTAA	4703
rs545126083	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151692820	ACTAAAAATACAAAA[A/T]TTAGCCGGGCGTGAT	4703
rs545129051	snp	C/T	0.0111196	0.0737302	intron-variant	NEB	GRCh38.p7	2:151609526	ATTTTAATCCTGTGG[C/T]AATTGACCCAAGGAA	4703
rs545152474	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151617121	GAAGGTTTTAAAAGT[A/G]TAATTCCTATGGAAA	4703
rs545176211	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151578675	AGACAAGGAGGGAAG[A/G]AGGGAAGGAAGGAAG	4703
rs545200284	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151693337	GGGAAGCGTGTGCCA[C/T]GGTGGTTTGCTGCAC	4703
rs545202321	snp	G/T			upstream-variant-2KB	NEB	GRCh38.p7	2:151735143	AGAACCTCTCTCATA[G/T]GTAACCGAGTTAGTG	4703
rs545214498	snp	C/T	0.000126555	0.00795371	intron-variant	NEB	GRCh38.p7	2:151568031	TCCCTGGGAGCAAGG[C/T]CCCACTTTTGCAAAA	4703
rs545244457	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151717238	AAACATTTATTAACA[C/T]AGTTCTTGACGTTTA	4703
rs545246394	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151565921	TTTTAAAGGATTTCT[C/G]TCTAGTAGTTTTCTC	4703
rs545269330	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151723162	CAGGTTTGCCACCTA[C/T]AAGAAGAGGGAACTG	4703
rs545282896	snp	G/T	6.62482e-05	0.00575497	intron-variant	NEB, RIF1	GRCh38.p7	2:151524480	GCCTTGGCAATGGCT[G/T]TTGGGGACTGGGGAC	4703
rs545293311	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151583864	TGTTTTCTTAGCCTT[G/T]GTATAAATTGGCTCA	4703
rs545299279	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151640304	CATTTTCTCCAAGGG[C/G]TGTTAAATAATTTCC	4703
rs545304760	snp	A/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151501316	GATTATTATAAAGGG[A/T]TGAACAGTGAGATGT	4703
rs545305923	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151716553	GAAATTTTACTATAC[C/T]TACTAGATCCTTTAT	4703
rs545320389	snp	C/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151530015	TCTCCTTCTGTGCTC[C/T]GGCAGTTATAGCTAT	4703
rs545323278	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151542266	AGGCTGCTGTTAACT[A/G]GGGTGAAGGATTGGC	4703
rs545350843	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151630931	TAAGCCAGACTTGAA[A/T]ATAAAGTATTCTACT	4703
rs545355758	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151684034	ACTTAGAAACAAAGC[A/G]TAGATTGGTGGTTGC	4703
rs545419056	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151645609	GGAACTACTTTAATA[C/T]ATTCTTTAATGTTAA	4703
rs545420980	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151637830	TGATGTTTTTAGTTT[C/T]TGGTGACAATTAAAA	4703
rs545436525	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151661774	CAGAAAGCAAGCTGG[A/G]GTTTGGGAGGTGGTT	4703
rs545439230	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151519282	ATACATACAATGGAA[C/T]ATTATTTAGCCATAA	4703
rs545445070	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151653028	TTTCCAACATTTCTG[G/T]AGTGCCAGAAATTAA	4703
rs545449022	snp	C/T	0.00279162	0.0372561	intron-variant	NEB	GRCh38.p7	2:151579157	TCTATAGGAAAATTC[C/T]GGTAGCACCTTTAAC	4703
rs545466072	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151643715	TGCGCTTGGGCATTA[G/T]TCCAGGGTAATTGTG	4703
rs545513893	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151686032	CCTGGTTTATAAAAA[C/T]AAAGTATGCAAACTT	4703
rs545521116	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151683324	CACTCGTTAATTTGC[A/G]TAAGAGGGCGGTTAT	4703
rs545535063	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime	NEB	GRCh38.p7	2:151733773	CAGACTTTTTCTTTC[A/G]TTTCTGTAGCTCTCG	4703
rs545536423	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151625710	TTTCAATTAAGACAC[A/C]ATGACAAAGTTGAGA	4703
rs545595071	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151666015	AGTGCAGCCAGGTGT[A/G]GGATGGAGTAAGTGG	4703
rs545597449	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151673422	TAACATGTGAAAAAT[C/T]ACTGTGTAAGTGCTA	4703
rs545605928	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151559914	CTCCACGTTCTGCAC[C/G]TGTACCCCAGAACTT	4703
rs545631716	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151666676	AAAGGTTCCTGAGAA[A/G]TTGGCTTATGAAGCA	4703
rs545652087	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151617659	GTTAAAGGACTTATC[A/G]GTTATGAAAAGTATA	4703
rs545692773	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151712724	TAGGTGAAGGAGTGA[C/G]AGGAAGAGAGAGGTA	4703
rs545694580	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151720833	CTTCTGCTTCCCTCA[C/T]AGATGTTCATGTCTT	4703
rs545715315	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151615182	ATGGTGTGGGCTTCT[C/T]CAGCTTAACAGCAAG	4703
rs545726685	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151680630	GTGTAATTGGGTCTC[C/T]TCATATTGTATAATA	4703
rs545734259	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151514981	ATCTTTATTACAATA[C/T]ATCTCTCCATCTCAG	4703
rs545763932	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151629334	TACTGGTTTAGGTTA[C/T]CCCCTTCCTACCTGG	4703
rs545764197	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151721832	AGCAAGAAGTACTCA[C/T]ACAATAAAATTGGTA	4703
rs545775533	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151734256	GTAGGGCCTTAGTAG[A/G]GCAATGGGGTTAAAC	4703
rs545777316	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151635630	AGAATCGCTTGACCC[C/T]AGGGGGCAGAGGTTG	4703
rs545785622	snp	A/C	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151676194	AATAGCTAAATTAAT[A/C]CCCAAATAATAAATA	4703
rs545805392	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151668901	ATGTTGCATGGTTAA[A/G]GGTTTAATGTGGAGG	4703
rs545889830	snp	A/G	5.50605e-05	0.00524664	missense	NEB	GRCh38.p7	2:151576158	TAACTCACAATACTA[A/G]TATTTTCAGCATTTG	4703
rs545897872	snp	G/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151509620	GAAGAGAGGTTTTTT[G/T]TTTGTTTGTTTGGTT	4703
rs545911622	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151634980	CTCAAAGACAACTGA[C/T]CGAGAAAGTGTAGGT	4703
rs545912181	snp	C/G	0.00119737	0.0244387	intron-variant	NEB, RIF1	GRCh38.p7	2:151517290	GCGAAGACCCTCATG[C/G]ACGCAGCACCTTGAT	4703
rs545913445	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151642267	CTACAATAAGCTCAA[C/T]TGTATATGAGAGATA	4703
rs545916295	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151634140	GTAGAAAAATAGATG[A/G]AATTCATGTAATTGT	4703
rs545916388	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151526105	TCATTAAGGCATCTG[C/T]CTGGGGCGTTCTCCC	4703
rs545925732	in-del	-/A			intron-variant	NEB	GRCh38.p7	2:151715772	CCCAAGCTGACTTAT[-/A]ATACTCAGTTTATAC	4703
rs545935553	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151553662	GAAACATGTGTACAC[A/G]GAGCCCTGCTTCCAG	4703
rs545936569	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151667681	TACAGGTACACGCCA[C/T]CACATCTGGCTAATT	4703
rs545937015	snp	A/G	3.31494e-05	0.00407107	splice-donor-variant, intron-variant	NEB, RIF1	GRCh38.p7	2:151505476	GAGAGTATGGCCACT[A/G]CCGAGCTAATGTGCT	4703
rs545974205	snp	A/T	0.00119737	0.0244387	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151503061	ACTCTACAATGCTAA[A/T]TCTGGAAATGAAAAA	4703
rs545992813	snp	C/T	0.00199481	0.0315187	intron-variant	NEB, RIF1	GRCh38.p7	2:151518821	AGATTAATGTTGTCA[C/T]TTGGAAGAATACACT	4703
rs545994198	snp	A/C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151530916	TTACACAGGAATAGA[A/C/T]AACTGGACCAGGGTT	4703
rs546003460	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151540635	TCAGAGGTAGCAGGG[A/G]AAGGTTTTAACAAAG	4703
rs546004791	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151626654	CCATTCTCCTGCCTC[A/T]GCCTCTTGAGTAGCT	4703
rs546035390	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151688092	ATTGGAGATCTTCTG[A/G]TAGTAACAGAGACCA	4703
rs546045636	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151536302	GCCCAAAAGTGGACA[C/T]GACGAAAACACTTCC	4703
rs546050688	snp	G/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151505798	CTTTGGGGCAGGGAT[G/T]GGGGCCCCTATTTAG	4703
rs546063461	snp	C/T	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151620714	AGCAAAGATCAAAAA[C/T]AAGGAGTCAAATGAG	4703
rs546066939	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151620277	AATATGAATATACTG[A/G]ACCCCACCAAACAGT	4703
rs546100235	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151628490	TAAGGGCAAACTGGA[G/T]ATTTTCTCCCTATTT	4703
rs546100702	snp	G/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151695157	CTTCTGCCCTTTCAA[G/T]CCCCTATATCTTTAT	4703
rs546113087	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151505146	TTTAGTTAAATTACT[C/T]GAGATCATCCCAATA	4703
rs546120601	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151669810	ATTCGTGTTTTAAGA[C/T]AGGCTCTTGCGATTG	4703
rs546128271	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151652506	CTGAGATTATGGGAC[A/G]GGGCCACTGCACCCA	4703
rs546132354	snp	A/G	3.50355e-05	0.00418527	synonymous-codon	NEB	GRCh38.p7	2:151655297	TGTTTGATTCTGCTT[A/G]GCTTGTAAAATATCT	4703
rs546139292	snp	C/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151511978	CTTAAAAGAGTTCTT[C/T]ACTACCTTAAAATTC	4703
rs546152104	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151626778	ATCCGCCTGCCTTGG[C/G]CTCCCAAAGAGCTGT	4703
rs546158995	snp	C/T	0.000399281	0.0141238	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151593091	GGTGAATTTGAGGGC[C/T]TCAGGCTTTATACGA	4703
rs546166920	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151704721	CCCTGCTTCGGCTCA[C/T]GCACAGTGCGAGCAC	4703
rs546186930	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151725052	CAGAGCATTACCCCA[A/G]TGACTCTAGGTCTGC	4703
rs546188898	in-del	-/T	0.00119737	0.0244387	intron-variant	NEB, RIF1	GRCh38.p7	2:151528663	TTCATTGTATAACCA[-/T]TTAATATATTTTTAA	4703
rs546202227	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151554219	ATAGCTGAAATAATA[C/T]GTAGCTTCTTTACAT	4703
rs546226673	snp	A/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151725729	ACTAAAATAGATTTG[A/T]TAATTGCTTCTCCTA	4703
rs546247045	snp	A/G	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151732373	GGATGTAAAATAAAT[A/G]TAAAATAAATGATTA	4703
rs546250852	snp	C/T	3.31362e-05	0.00407026	missense	NEB	GRCh38.p7	2:151725487	ACTTTTTTGATTCTG[C/T]GAAGTTCTGGAGTAT	4703
rs546253308	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151567740	AAATAGAGAAAAAAT[A/G]TATACTTGTTCTCTG	4703
rs546268078	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151719379	TCCCTTCCTCATGGC[A/T]GTGTTCTTATTTATC	4703
rs546284369	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151718125	CCCAAAGTGCTGGGA[A/T]TACAGGCGTGAGCCA	4703
rs546292006	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151567066	GAACAAATTAAATAT[C/T]GATGGCCTCAAATTT	4703
rs546316138	in-del	-/G	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151723259	AATTCTAGACATACT[-/G]CCTCTGAAATACAAC	4703
rs546329629	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151718638	TTCAGAGGGAATGAC[C/T]CCTGCACCCAGGGTG	4703
rs546363216	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151655612	ATAATAATTAAAAAC[A/G]TAAATAATTTCTAAC	4703
rs546371080	snp	C/T	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151681043	TTGGGACAGCACAGA[C/T]ACATATACTGCTCTC	4703
rs546378956	in-del	-/T	0.000880772	0.0209669	intron-variant	NEB	GRCh38.p7	2:151697506	TGAAATAATGGGTTC[-/T]TTTTTTTAACAGAAA	4703
rs546393433	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151612514	AATTTCTGGGAAGAC[C/T]CACAGGATTGCTTTA	4703
rs546404193	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151649130	CCAACAAGGGGGAAA[C/T]ATTTTGTACAAATTT	4703
rs546406285	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151538572	AACTCTGTACAATTT[C/T]GGTAAATCTAAGACT	4703
rs546421187	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151489404	TGCATACATCTATAC[A/G]TTCTTGATTTTTGAG	4703
rs546422983	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151496440	GAGGTTTTAAGGGTA[A/G]GGTCAACTTCCTTGT	4703
rs546424421	snp	C/T	0.0103295	0.0711199	intron-variant	NEB	GRCh38.p7	2:151551148	AATTTTTTGTATTTT[C/T]AGTAGAGATGGGGTT	4703
rs546435412	in-del	-/G			intron-variant	NEB	GRCh38.p7	2:151558924	AACACCAAAAGCAAT[-/G]GCAACAAAGGCCATT	4703
rs546460398	snp	C/T	0.0146672	0.084371	intron-variant	NEB	GRCh38.p7	2:151595477	GAGGTTTTACCATGT[C/T]GGCCAGGCTGGTCTC	4703
rs546472674	in-del	-/TT			intron-variant	NEB, RIF1	GRCh38.p7	2:151517729	TGTAACACAAGAGTA[-/TT]TGTGTATCTTGATAC	4703
rs546478649	snp	G/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151489853	ACATGTAATAAAAGA[G/T]CATTATATAAAATAG	4703
rs546484256	snp	G/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151495782	CCAAAACTACTATTG[G/T]ATCATAATTTATATC	4703
rs546496124	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151548810	ATTTTAACACATCCT[C/T]TAGGTGTTAGATTAT	4703
rs546500075	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151704869	GGAGCTGTTCCTATT[C/T]GGCCATCTTGGCTCC	4703
rs546510007	snp	A/G	8.28274e-05	0.00643481	synonymous-codon	NEB	GRCh38.p7	2:151725516	ATCTGTTGTGCTGGC[A/G]TATGGCTGTCCTTTT	4703
rs546540315	snp	A/G	0.00478085	0.0486577	intron-variant	NEB	GRCh38.p7	2:151554477	GGTGGGATGATTCCC[A/G]GAGCCCAAGAGGTAG	4703
rs546571019	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151611418	TTGCTGTTATCATTG[C/T]GGTTGCTGTTGATGG	4703
rs546610700	snp	A/G	8.31584e-05	0.00644766	intron-variant	NEB	GRCh38.p7	2:151561111	CTTTATATTTTACCT[A/G]TAGACAAGCAACAAT	4703
rs546618139	snp	A/G	0.00279162	0.0372561	intron-variant	NEB	GRCh38.p7	2:151661697	GATTACCCAGAGAAC[A/G]TCCTGGTTTGAAATG	4703
rs546621564	snp	C/T	9.09116e-05	0.00674148	intron-variant	NEB	GRCh38.p7	2:151667786	ATAGAAAGTTTCCTA[C/T]TTTTAAGTTAGACTT	4703
rs546621865	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151674973	TTTTAAAAGGGAGCT[C/G]ATTTATTCTTATGTT	4703
rs546626927	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151615513	GACATCTCACCAATT[A/T]GGAGTTACAAAGGAC	4703
rs546628365	snp	A/C	1.82623e-05	0.00302173	intron-variant	NEB	GRCh38.p7	2:151609780	CTACATCTTCCCCTT[A/C]CCCCTTTCCCAAAAT	4703
rs546635720	snp	C/G	0.021333	0.101051	intron-variant	NEB	GRCh38.p7	2:151702592	TAGTTAGCTCTTCTT[C/G]TGGAATTGATCCCTT	4703
rs546641596	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151552457	GTTACTTCATAGACT[C/G]GCATCACCTACAACT	4703
rs546650833	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151659993	TTGTGGTGGACATGG[A/C]GATGTGCCACCAATA	4703
rs546657259	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151618653	TTTTTTTTTCTGAGC[A/G]TTTTTTTGGTACAGA	4703
rs546730539	snp	C/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151611940	CCAGGTCACTGCTCA[C/G]AAGGGTGAGTGCATC	4703
rs546738723	in-del	-/TC	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151713596	ACCTGAAATCTCATA[-/TC]TTTTTTCTTTTGTGG	4703
rs546747977	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151516333	GAGAAGATTTTAGTG[A/G]TCACATGATAAAAAG	4703
rs546748774	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151716822	TGGTCTGATTTGGAC[C/T]AATTTAAAATAGGAA	4703
rs546749783	snp	A/T	0.00199481	0.0315187	intron-variant	NEB, RIF1	GRCh38.p7	2:151524698	TTGAGATGGAATCTC[A/T]CTCTGTTGCCCAGGC	4703
rs546750696	snp	C/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151662474	CTTCAATATTTGCTT[C/G]AATATTGGTATTTAA	4703
rs546787322	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151655537	AAACAAACTCAGATT[A/T]AAAAAAAAAATCTTT	4703
rs546801327	snp	A/C	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151538665	AAAAACCCAAACAAA[A/C]AACATTGTTGAGCCC	4703
rs546831156	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151574042	ACAGTGGCGTGATCT[C/T]GGCTTACTGCTAGCT	4703
rs546840028	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151547313	CCAACTTGTACTCTT[A/T]GTTTAGAAGTGCTTA	4703
rs546861596	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151577244	ACTAGAAGGGATGAA[C/T]GGTCTGGCACCAGTC	4703
rs546864277	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151704733	TCACGCACAGTGCGA[G/T]CACTCACTGACCTGC	4703
rs546864597	in-del	-/T	0.00119737	0.0244387	intron-variant	NEB, RIF1	GRCh38.p7	2:151489668	CCCAAAGTGCTGGCA[-/T]TTATAGGCATGATTC	4703
rs546869744	snp	A/C/G	0.00013452	0.00820022	missense	NEB	GRCh38.p7	2:151570269	TGGCCCAGTCCAGCC[A/C/G]GTACTCTCGTTCATT	4703
rs546872372	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151702927	GATGTTAGCTTGCTC[A/G]TTAGTTGATGCAGTT	4703
rs546876604	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151546781	CCAGGCTGGTCTCGA[A/T]CTCCTGACCTCAGGT	4703
rs546883371	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151711083	GACTCCCAAATCCCA[C/T]TCCATCTGAATCCCA	4703
rs546956355	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151668537	AGGATTTATCAATAT[A/C]CTTTTTTTAAAAAAG	4703
rs546965949	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151666506	TTCAGTCTGAATCTA[A/G]GTAACATCGAAGTTT	4703
rs546970274	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151544192	CTCAGTGCTGATGCA[A/C]AACTTGCCCAAAATC	4703
rs546970989	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151617987	ATTGCTTGAACCCAG[A/G]AGGTGGAGGTTGCAG	4703
rs546992311	snp	A/G	0.0570934	0.159019	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151579593	AGGGTCTTCCTTGGC[A/G]CTGCGACAGCCAATG	4703
rs547001246	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151523223	AGTTTCAAATACTTA[C/T]ACAATTCCATTAATT	4703
rs547020660	snp	A/G	1.65699e-05	0.00287831	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151529251	TGGCTGCTTTGATAT[A/G]AACAGCATCTGGCTC	4703
rs547028135	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151696927	ACTTTCCTATATCTT[C/T]GGGTTTCCAATAACT	4703
rs547028423	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151653592	GCCTATTTTAAAATA[C/T]GTGCATATAAAATCT	4703
rs547036219	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151546661	CCTCCCGAGTTCAAG[A/C]GATTCTCCTGCCTCA	4703
rs547049780	in-del	-/T	0.00795532	0.062565	intron-variant	NEB	GRCh38.p7	2:151668768	CTGTCTCATGTTCCA[-/T]TTTTTTTTTAAATGG	4703
rs547052441	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151548885	GGTTATTGGGTCCTT[C/T]CTGGCCACTAGGTTT	4703
rs547068600	snp	C/T	0.00119737	0.0244387	intron-variant	NEB, RIF1	GRCh38.p7	2:151501721	TGCCGGCAGGAGTGG[C/T]TTGACTTATGTAGGC	4703
rs547078436	snp	C/T	3.37206e-05	0.00410599	missense	NEB	GRCh38.p7	2:151717420	TATTTACTTACCTTG[C/T]TCACTTGATTGGTTA	4703
rs547080730	snp	A/G	0.00517822	0.0506191	intron-variant	NEB, RIF1	GRCh38.p7	2:151508505	TCAACAGGCAGGCGG[A/G]GAGAAGCTGGAGGGT	4703
rs547102749	snp	A/G	3.3157e-05	0.00407154	intron-variant	NEB	GRCh38.p7	2:151679873	TTAGAGACTGTGTTA[A/G]TAAAGTCTGGACATA	4703
rs547109690	snp	A/G	0.00284645	0.0376181	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151617412	CATGATTTCTGGTGT[A/G]TCAGGCATGACATGA	4703
rs547143001	snp	C/T	7.68649e-05	0.00619892	missense	NEB	GRCh38.p7	2:151691925	ATTGTCTGAGGGAAA[C/T]AGCATTTTCCTTTAT	4703
rs547170182	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151497935	GGAAGGGCTGTCAGA[A/G]TTATCCATGTTATTT	4703
rs547183534	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151523893	TATGTTTAATGAAAA[A/G]AAAATGAATATTTTC	4703
rs547231033	snp	A/G	0.000399281	0.0141238	missense	NEB	GRCh38.p7	2:151570592	CATCCCAGCCCTCAC[A/G]GTAAAGTTTCTGAAA	4703
rs547284355	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151527207	GCCTAGCTGCCAGGA[C/T]CAAGCCCCTCCATCC	4703
rs547286016	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151610319	TTCATTGGTGAAAGC[A/G]TTCCCTGCAGCAACT	4703
rs547288176	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151620525	GTTCTGTGCACCACA[C/T]AGAAAGAAGACTTTG	4703
rs547290800	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	NEB	GRCh38.p7	2:151736234	AAAGCAAAACAATGC[A/G]AAACAAAACACACAG	4703
rs547304933	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151691259	AGCTTGTTCTCTCCT[C/T]AGGCCGTTCTTCCCT	4703
rs547323004	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151605772	TGGAGCTGGGGGCAG[G/T]GTGCACCTGGTAGCA	4703
rs547326393	snp	A/T	1.69725e-05	0.00291306	missense, intron-variant	NEB	GRCh38.p7	2:151650633	TCTGATCAGGCAGAC[A/T]TGTCCACTGATGCAG	4703
rs547326621	in-del	-/A			intron-variant	NEB	GRCh38.p7	2:151595767	AAATATTTTAGGGAT[-/A]AAAATGACATTGTAT	4703
rs547341741	snp	C/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151494950	ACCACACCTGGCCCA[C/G]AGCAGCTGTTTTTTT	4703
rs547353501	snp	A/G	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151577682	CTCCTAGGTTCAAAC[A/G]ATTCTCCTGCCTCAG	4703
rs547356589	snp	A/G	0.0023933	0.0345097	intron-variant	NEB, RIF1	GRCh38.p7	2:151517984	GTTTGAAATCTTCCT[A/G]ACTCCCTATAATCTA	4703
rs547368083	snp	A/T	1.7688e-05	0.00297383	intron-variant	NEB	GRCh38.p7	2:151653976	ATAGCCTTATAGAAC[A/T]CAAACTAGTACTCAC	4703
rs547373183	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151649333	AATGCTCATTCTAAG[C/T]TGATTATGGGCTTAT	4703
rs547390770	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151634676	ATAAAAACAGTAAAA[C/T]GAGTGACTGATTCCT	4703
rs547392955	snp	C/T	0.000304136	0.0123278	missense, intron-variant	NEB	GRCh38.p7	2:151606653	GCTTGATTTCAATGG[C/T]ATCTGCCCTTATGTC	4703
rs547421303	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151533021	TGCACGGTAATCCTC[A/G]TCTCCCTGCAACAGT	4703
rs547441716	snp	A/G	1.67354e-05	0.00289265	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151526180	ACCAGGTTGCTGACA[A/G]TCTTCGCCAGCAGGA	4703
rs547477093	snp	A/C	0.000399281	0.0141238	intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151497233	TGCACCCTCTAGAGA[A/C]GCAGGGACCTCAGCT	4703
rs547478187	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151531613	TAAGCCACCACGCCC[A/G]GCCACAACAATTCTT	4703
rs547481191	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151706158	TATACCCTCTCACTT[G/T]CCACTTTCCCACACC	4703
rs547506442	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151613770	ACTTCCCCCTTTGCT[C/G]TCTCTCTCCTGCTCC	4703
rs547507758	snp	C/T	1.66045e-05	0.00288132	missense	NEB	GRCh38.p7	2:151663670	CCTGAGACTTCTTGG[C/T]TGCCACCACACTGAG	4703
rs547541231	snp	C/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151620861	CAAAGAGACATCCAG[C/G]TGTATTCTGTGTGGC	4703
rs547541336	snp	A/G	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151512250	CGTGTTAGCCAGGAT[A/G]GTCTGGATCTCCTGA	4703
rs547544106	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151636809	AAAACAAAAAAAAAA[G/T]ATACCCATAAAGCCC	4703
rs547548701	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	NEB	GRCh38.p7	2:151735428	ATCTAATTCTATCTG[C/T]CTGTCTGTCTGTCCT	4703
rs547556599	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151705106	ATAAGGTGAGAAATA[C/T]GCAATCTCCCTCCCT	4703
rs547586036	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151670064	TTTATTGTGATGTGG[A/G]AGACTTTATATAGTG	4703
rs547589242	snp	A/G	0.00358779	0.0422022	intron-variant	NEB	GRCh38.p7	2:151689260	CCCAGGCTGGAGTAC[A/G]GTGACACAATCTCGG	4703
rs547589562	snp	A/G	1.65611e-05	0.00287755	missense, splice-donor-variant, intron-variant	NEB	GRCh38.p7	2:151644071	TTGGGGTCATCTTCA[A/G]TGTTCCGGGCACCAA	4703
rs547625126	snp	C/T	1.66527e-05	0.00288549	synonymous-codon	NEB	GRCh38.p7	2:151656432	ACCAACCATTTTCCC[C/T]TTCCCTTTTTCATAA	4703
rs547639762	snp	A/G	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151628685	GTCTCTACTAAAAAT[A/G]CAAAAAATACTAAAT	4703
rs547642912	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151676368	CCTTCCTTGGATTTC[A/G]GTGACAGCCTTCTAA	4703
rs547714053	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151526638	CATGGCGTTTCCATA[A/G]AGAGTCCAGCCAGGC	4703
rs547715993	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151723607	TGAGAGCAAAGGTAA[A/G]TGAAATTCACAGATA	4703
rs547724356	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151734379	GAGTATTACAGAAAA[A/G]GTCATAAACTGGCCT	4703
rs547728786	in-del	-/AT			intron-variant	NEB, RIF1	GRCh38.p7	2:151503507	TTAGATAGCAGCCAC[-/AT]GTGGGCTATTTGGGG	4703
rs547758981	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151548774	CTGACAAATAGCTTC[A/G]TGGACTGATTTTAAC	4703
rs547779805	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151708213	ATGCTTTTGTTTCGT[A/G]TCTTAAAAAGTCCCT	4703
rs547791393	snp	G/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151734022	GCAGTGGCTGGTTTT[G/T]TTAAGCTAGCGAAAC	4703
rs547829189	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151620750	TTCCAGTCTAGGCTA[C/T]GCCTCTGTGATGCTT	4703
rs547833033	in-del	-/TGTT	0.00199481	0.0315187	intron-variant	NEB, RIF1	GRCh38.p7	2:151501333	AACAGTGAGATGTTC[-/TGTT]TGTTTTGTAGAAATT	4703
rs547834650	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151555141	GAAAAACCCGACTCT[C/G]AGATCCACCCAGCGT	4703
rs547852316	snp	C/T	2.67255e-05	0.00365541	missense	NEB	GRCh38.p7	2:151568632	CATCATCGAGGATCT[C/T]GCCACTTTGTTTCGC	4703
rs547877070	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151675661	CAACCATGAAACCCT[A/G]GCAAGAATAATAGAA	4703
rs547888290	snp	C/T	0.00018401	0.00959015	intron-variant	NEB	GRCh38.p7	2:151594341	AGTAAGAAATCATAT[C/T]AAAAAGACATATGAA	4703
rs547889316	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151712169	TTTGGAGAGACATGG[A/C]CCTACCTCTTGCTTG	4703
rs547889698	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151666520	AGGTAACATCGAAGT[A/T]TTTTTTTGTATTTTA	4703
rs547891086	snp	C/T	4.96948e-05	0.00498447	intron-variant	NEB	GRCh38.p7	2:151575682	CAAAAAGAGAGTCTG[C/T]TGTAGTACTTACATT	4703
rs547920691	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151556274	GCATTTAAATGAGTA[C/G]AACAGAATGGAAATT	4703
rs547922604	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151712774	CTCTACCAGCGAAGG[A/G]GTCCCACTCTGCAAG	4703
rs547952084	in-del	-/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151524684	TTTTTTTTTTTTTTT[-/T]GAGATGGAATCTCAC	4703
rs547972269	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151628269	GAGTCCACAGATACC[A/G]TTTTATCCCTCCATC	4703
rs547975375	snp	A/G	0.0119091	0.0762411	intron-variant	NEB	GRCh38.p7	2:151620345	TATATATGTATGTGT[A/G]TGTATATATATATAT	4703
rs548008163	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151727559	AGTCACAAGAGCCTA[C/T]AATTTGCAAAATAAG	4703
rs548008246	snp	A/G	0.00478085	0.0486577	intron-variant	NEB	GRCh38.p7	2:151719736	ATACAAAAATTAGCC[A/G]GGTGTGGTGGTGTGC	4703
rs548011009	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151638696	GGGTGGAGGCTTGAC[A/T]CTCTGCCTAAGCCTC	4703
rs548014686	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151703210	TCTTCTGGCTTGTAG[A/G]GTTTCTGCTGAGAGA	4703
rs548030104	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151577133	GCAGCCAGAATGATC[C/T]TTTCAAAATTCAGAA	4703
rs548046655	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151527695	TCTCAAATCATGATT[C/T]CTAATGCAAGAGGAA	4703
rs548049758	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151705991	CTGTAGGTGATGGGT[A/G]CACCAAAATCTCAGC	4703
rs548052618	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151672835	AAAGTTCAGTGAAAA[C/T]ATATATTGGAGTTAC	4703
rs548061398	snp	A/G	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151683458	AAAATTCAAACTGTT[A/G]TTTTTTACTCTGGGC	4703
rs548066315	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151605640	GAATCAAGCAGATAA[C/T]GTGGACTAGCTATGG	4703
rs548084149	snp	C/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151532114	TTTTTTGTTTCCCTC[C/T]GAGACGGAGTCTTAC	4703
rs548093589	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151603825	AAAGTTGCCCATAAG[A/C]GTTTGATGCTTGCAA	4703
rs548107210	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151635179	AATGCATATAAAGCT[C/T]TTAGCAAAGAGTTCT	4703
rs548112806	snp	A/G	3.32596e-05	0.00407783	intron-variant	NEB	GRCh38.p7	2:151569263	AGGGTAAAATCTTGG[A/G]ATACCTCACTGAAGA	4703
rs548142273	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151524965	GCCACCACGCCCAGC[C/T]GAGATATGCTATCTT	4703
rs548144157	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151540130	CATATTTTTATTCAG[A/G]AGAGAATTGAGAAGA	4703
rs548145659	snp	C/G	0.00199481	0.0315187	intron-variant	NEB, RIF1	GRCh38.p7	2:151491542	TTGCTCACTAGTTAA[C/G]AAGGTATTTTTATGC	4703
rs548217762	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151656534	TCTAGTGTCAATATG[C/T]TATATTATTTTTGTA	4703
rs548243788	snp	G/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151497201	TACTTTAGTGGAAGT[G/T]GTTGGGATGGGGAAT	4703
rs548244023	in-del	-/AATGT	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151625813	TTGTAACAAAATATA[-/AATGT]ATACTAAGATATGAA	4703
rs548258921	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151620036	AATTACAGTAATAAA[C/T]CATGATGGTGTCTCA	4703
rs548272880	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151557592	TTAGACCAATATCCC[C/T]GATGAACATCGATGT	4703
rs548279259	snp	A/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151495657	GTTAAAGACTACAGT[A/T]AAACTAAAGAACAAC	4703
rs548306000	snp	A/C	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151504677	GCCATAAACTATTTC[A/C]CAAACTTCACATAGT	4703
rs548318087	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151504107	TAAGGAACCTCCACT[C/T]TCTGAGCCTCCTTAA	4703
rs548319430	snp	C/T	0.00119737	0.0244387	intron-variant	NEB, RIF1	GRCh38.p7	2:151489889	TTGGTTAAAAAAAAC[C/T]GTAATACCTAATACT	4703
rs548343514	snp	A/G	0.000399281	0.0141238	missense, intron-variant	NEB	GRCh38.p7	2:151642773	TACTTACCTCACTGT[A/G]ATTTACTTTGTTTTG	4703
rs548363954	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151554720	CTTTTCTATGTTTAG[A/G]TACACAAATACTTGC	4703
rs548389227	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151650036	AGTTGCTAATTCAAA[C/T]AAAATGATCCAATAT	4703
rs548410154	snp	C/T	0.000217984	0.0104376	intron-variant	NEB	GRCh38.p7	2:151690607	TTATTAAACAAATCT[C/T]GAAAAATAATAATAT	4703
rs548426281	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151650487	ATTTTCAATAATAAT[C/T]CCTAATTTCTGCTTC	4703
rs548487053	snp	A/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151490762	CCAGGTTTCAAATCC[A/T]AGAGTCTATTTGTAA	4703
rs548491697	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151726013	ATTAATGGCAGATCT[G/T]AATTATATTCTGTAA	4703
rs548491801	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151682903	CATTAAGGTTATTTT[A/G]TATATTTCTTTGGTG	4703
rs548496222	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151701814	ATCCTTTCAAAAAAC[C/T]AGCTCCTGGATTCAT	4703
rs548502763	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151641930	TAACTGATCATTTAC[C/G]TTAGGTATATCTCCT	4703
rs548532933	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151717325	GTGTTTGTGTTTTAT[C/T]TTCAGTCTCACCTTT	4703
rs548535400	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151569071	CCAAGCATCAGTGAG[G/T]GTGCTGGATATTATA	4703
rs548535958	snp	A/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151521398	TTCTCTGAAAAAGTT[A/T]CACTCTCAACATAAA	4703
rs548548066	snp	A/G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151645187	ATAGAGAAATGAAAT[A/G/T]GATTATTATTGAGGT	4703
rs548548742	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151656930	TTTACTGATGAGAAA[A/C]GTTTCAATTATGAGA	4703
rs548573941	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151527690	AAACATCTCAAATCA[C/T]GATTCCTAATGCAAG	4703
rs548609014	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151695320	CAATTAAGCATACAT[C/G]AGACGTAGCATTCTG	4703
rs548650238	snp	A/C	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151593640	TCTATATCCATCCTG[A/C]CCCCCATCTCTCTCT	4703
rs548652177	snp	C/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151489254	AGGCTTTTGAGGATA[C/T]TATGAATGAGATCCA	4703
rs548687115	snp	A/G	0.000101036	0.00710687	stop-gained, intron-variant	NEB	GRCh38.p7	2:151591404	CAATGGCATCTGCTC[A/G]CAGGTCATAACCAGT	4703
rs548707428	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151704730	GGCTCACGCACAGTG[C/T]GAGCACTCACTGACC	4703
rs548714740	snp	A/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151510779	TAATTTCAGGCATCC[A/T]CTAGAGGTCTTGGAA	4703
rs548720543	snp	C/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151515272	ACACCTTTCTTAAGG[C/T]GACAAAAGACTTTAT	4703
rs548726582	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151680243	CAGTTTTGCAAAGAT[C/T]CCTTGGAACTTGCAG	4703
rs548768085	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151635019	AAGAGACAATATGGT[A/G]CAGTGGAAAGGAATG	4703
rs548769915	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151530938	ACCAGGGTTTGTTAC[A/G]TCTCATTAGAAGGAG	4703
rs548791409	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151561745	CTGAAAAGTTTTCCA[A/G]ATACTGATCTTTTTC	4703
rs548807123	snp	C/G	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151634614	GCCACTGCACTCCAG[C/G]CTGGGTGACAGCAAG	4703
rs548833828	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151726601	GACCCATTGAAATGT[A/G]TCTGAATCTGTCTGA	4703
rs548836588	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151568508	GCATCCATCATTTCA[A/G]TGATTAAAATCTGTA	4703
rs548846329	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151644781	CTAAATCAGCAAAAT[C/T]GTCAGCTCTTCCCAA	4703
rs548848498	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151689049	CTGCCAGCTGCCATT[G/T]CATAGATTCTGTTAT	4703
rs548934119	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151629752	AGGATAGGAACTGGA[A/G]ACAATTCAAGTTTCT	4703
rs548934775	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151689910	GGTATGAGCTAATTT[G/T]TGTCATTAAAATATA	4703
rs548935919	snp	C/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151521135	CTAACACCAGTACCC[C/G]TCATGGTTCATCACT	4703
rs548943007	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151559027	AATGGGAAAAAATTT[A/C]TGCAATCTATCCATC	4703
rs548964642	snp	A/G	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151728288	AGCAAACTTGAGTTC[A/G]GGGAACAAAAGGTTA	4703
rs548969150	snp	C/G	0.000798403	0.0199641	intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151534502	GATTACCTGAAGAAG[C/G]CTGGAGTGTGGGATA	4703
rs548977523	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151644405	CAATTTAAAATTAAA[C/T]TGAGACTGCTTTGAA	4703
rs548981872	snp	A/G	9.17347e-05	0.00677192	intron-variant	NEB	GRCh38.p7	2:151565466	ACAATTTACTCCCCA[A/G]TCTGTGCACTTCAGC	4703
rs549001664	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151729088	AAAAAAGAGCTTGAA[C/T]GTGGAATATTTATGG	4703
rs549010236	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151486744	TCAAAAGTAAAGGAC[A/G]CCATGCACCAAGGTC	4703
rs549010673	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151693664	CTTTATACAATCTAT[C/T]GTTGTTGATTCCTTG	4703
rs549037740	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151578868	GGGTGGATCACCTGC[A/G]GTCAGGAGTTCAAAA	4703
rs549040858	snp	A/T	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151609124	TAACATTTAAAAAAA[A/T]TTTTTTAAGGGATGG	4703
rs549060633	snp	A/G			intron-variant, utr-variant-3-prime, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151498017	AGACTGTTAGAACTC[A/G]GTGTTGTTATCCACA	4703
rs549074640	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151578352	GGAAGATGGTCCTGC[C/T]CTTCTTTGATTCATA	4703
rs549080092	snp	A/T	0.00019918	0.00997749	intron-variant	NEB	GRCh38.p7	2:151692023	GGCTCTCAAACAATG[A/T]CACTGTGAGGCATGA	4703
rs549082598	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151698053	CCCGGGCGACAATGC[A/G]AGACTCCGTCTCAAA	4703
rs549092959	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151625358	TGTCTAATCTATCTA[C/T]CTTTCTATCTGCCTA	4703
rs549110906	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151659220	CTTAAAAGAAGCTCA[C/T]TTAGTACATACATAT	4703
rs549112309	snp	A/C	0.00874735	0.0655527	intron-variant	NEB	GRCh38.p7	2:151636798	AAAAACAAAACAAAA[A/C]AAAAAAAAAAGATAC	4703
rs549119346	snp	A/T	0.00279162	0.0372561	intron-variant	NEB	GRCh38.p7	2:151698816	CTAATTTTTTTGTAT[A/T]TTTAGTAGAGACAGG	4703
rs549129112	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151631807	AATATGAAATTTTAA[A/G]GTAGCACATAAAACA	4703
rs549136313	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151682930	GGTGAGATATAGTAA[A/C]AGCTCTTCGATTTTT	4703
rs549149709	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151559519	CAGCACTCTTCACCA[C/T]AGCAAAGTCTTGGAA	4703
rs549162403	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151624423	AACTAACTTCATCTG[C/T]CTTGGATAAAATAAA	4703
rs549163678	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151577598	TTTTTTGTTTGCCTT[C/T]GAGACGGAGTCTCAC	4703
rs549170732	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151543073	CTTGACTGTTCCTAT[A/G]TAAAGCCATTTATCA	4703
rs549199184	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151730740	AATTTCCCTCAATGG[A/C]CTGCATTCTTTTCAG	4703
rs549227905	snp	C/T	0.00018222	0.00954342	missense, intron-variant	NEB	GRCh38.p7	2:151643275	TCTGGGTGGCTCGTT[C/T]ATTTTTCTCATCCTC	4703
rs549231016	snp	A/C/T	9.34872e-05	0.00683638	missense	NEB	GRCh38.p7	2:151684780	CCTGGTTACTCACAT[A/C/T]GCTCTGCAGCGCATA	4703
rs549257129	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151623023	AATTTAGAAGAGTGT[A/G]TGTATGGAAGTTGAA	4703
rs549261822	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151615719	ATTTTTTTTGAAGAC[A/G]GAGTGTTCAATTTCT	4703
rs549285971	snp	C/T	1.866e-05	0.00305445	missense	NEB	GRCh38.p7	2:151664824	CAGGCATGACATGAA[C/T]GGTGGTCTTGTCCTT	4703
rs549288015	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151542775	AAGTCTGAGACACAT[A/G]TTTTCTTAATGCTCA	4703
rs549295899	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151622270	TGGGATTTCAGGCAT[A/G]AGCCACTGCACCCAG	4703
rs549346797	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151658197	TTTTGTTTTTGAGCA[A/G]AATGCTTCGTTGGTG	4703
rs549351171	snp	A/G	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151527330	TTGGGTTCTGAGCTC[A/G]CCTATCGCTCCCCCA	4703
rs549356470	snp	C/T	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151677278	GTTTGCATGTGTATG[C/T]GTGTAGTCCTAGAAT	4703
rs549390899	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151721402	TCCCATCATTCATTT[C/T]CCTTGTCCCTCAAAA	4703
rs549419196	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151548553	GTAGAAAAGTCATTG[A/G]CAAAATTTCAATATT	4703
rs549421094	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151714587	TCCAATTAATCTGCC[C/T]TTTGCAAGCTGATTT	4703
rs549421303	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151562865	GTAAATTATTCAGAT[C/T]AATGTCTTTTAGATC	4703
rs549447969	snp	A/G	0.00358779	0.0422022	intron-variant	NEB, RIF1	GRCh38.p7	2:151512415	ACTGCAGCCTCAACC[A/G]CCTGGGCTCAATTGA	4703
rs549474703	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151574574	AGCCTTTTCTTCTTG[C/T]TCTATGGCACTATTA	4703
rs549485763	snp	A/C	1.65963e-05	0.0028806	missense	NEB	GRCh38.p7	2:151697544	AGTAGGATTGCTTAC[A/C]TCACTACTGAAGTTC	4703
rs549488623	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151520231	TTAGGAGAATTTATT[A/G]TTATTTTAAAATAGT	4703
rs549497202	snp	A/T	1.73951e-05	0.00294911	missense, intron-variant	NEB	GRCh38.p7	2:151636234	CAACTCACGTCACTG[A/T]TGATGTCCCTGGAGG	4703
rs549507691	snp	G/T	1.86565e-05	0.00305416	missense	NEB	GRCh38.p7	2:151664799	CTGGAGAGTAAAATA[G/T]CCGGTGTGTCAGGCA	4703
rs549517158	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151631412	GGGTAAATATGCAAA[G/T]AGAATCAGTAATAAA	4703
rs549525441	snp	A/G	1.65814e-05	0.00287931	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151519728	GGATTGTATTTTGGT[A/G]TCTTGCCCTTTTCTT	4703
rs549568631	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151541719	TCCTGCACCCTCCTT[C/T]TCTTTTTTCCCTTGT	4703
rs549597397	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151546839	GCTGGGATTACAGGC[A/G]TGAGCCACCGTGCCC	4703
rs549603593	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151557733	GCAAATCAATAAATG[C/T]AATCTATCACATAAA	4703
rs549612614	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151498810	CACTTTCAAAAGAAG[C/T]CAGAGTATTTAATTT	4703
rs549621880	snp	C/G	0	0	intron-variant	NEB	GRCh38.p7	2:151714018	ATTTTGAATTAAAGG[C/G]CCTTAGAGATTAATG	4703
rs549640295	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151614856	TTATTATACCACACT[G/T]CTCAGTTTACATTTG	4703
rs549643594	snp	A/G	0.00438332	0.0466095	intron-variant	NEB	GRCh38.p7	2:151707234	ATCCATAGGGTGTCA[A/G]TTCTGTTTCTGGCTT	4703
rs549650292	snp	C/G	0.00119737	0.0244387	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151506714	AAGTTACGTTGTTAG[C/G]AGATTTAAAGTTATT	4703
rs549651526	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151541638	CTGCTTTTACATAGA[A/G]AAGGCAGGAGCCCTC	4703
rs549676026	in-del	-/C			intron-variant	NEB, RIF1	GRCh38.p7	2:151518166	TGTTGTAATTTATAA[-/C]ATAAGAATTTGTTTC	4703
rs549685288	snp	C/T	0.00279162	0.0372561	intron-variant	NEB	GRCh38.p7	2:151664340	TAATGAACAGATGAT[C/T]AGAGGGTACTTGGAT	4703
rs549712411	snp	C/T	7.2812e-05	0.0060333	intron-variant	NEB, RIF1	GRCh38.p7	2:151527629	CTTGATTCAGTAGGC[C/T]AAATTCATAAACACA	4703
rs549721052	snp	C/T	0.00279162	0.0372561	intron-variant	NEB, RIF1	GRCh38.p7	2:151521339	GCACACTGAGACACA[C/T]AAAGTAAAGGAAAAA	4703
rs549722074	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151659458	GGCATGCACTACCAT[A/G]CCTGGCTAATTTTTG	4703
rs549723235	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151730143	AATAATAAGATCCCA[A/C]GGTATATCCACATCT	4703
rs549728563	snp	A/G			intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151498613	AATCTCTGCAGCACT[A/G]AGCAACCGTGAAAGA	4703
rs549733394	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151671572	TGAAGCCTAATAAAA[C/T]AGAAATGATCATGCT	4703
rs549736667	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151636029	TTTTCACAGAAGACG[C/T]TGTGTCCTGTAGGTT	4703
rs549740944	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime	NEB	GRCh38.p7	2:151734453	TCCCAACTCTCCCCT[C/T]CTGAGAACCCCAGGC	4703
rs549741138	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151629878	ATATATTAACCTATT[A/G]TATATCATTATAGAT	4703
rs549769231	snp	C/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151542533	ATGACTTGTTGATAT[C/G]CCAGTTACTCGGGCC	4703
rs549773768	snp	C/T	0.0209421	0.100162	intron-variant	NEB	GRCh38.p7	2:151647268	GGCACCCACCACATG[C/T]CCAGCTAATTTTTGT	4703
rs549777377	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151493115	TGGCAATTAACTTGT[C/T]ATGTTTAGTATGATG	4703
rs549778793	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151571505	AATTCAGTTTTGTAA[A/C]CTTCAGAATTGTAAA	4703
rs549794342	snp	A/G	0.000816586	0.0201897	stop-gained, intron-variant	NEB, RIF1	GRCh38.p7	2:151501423	GATTGAGTTTGACTC[A/G]CTCCATCTCAGGAGT	4703
rs549795769	snp	A/T	0.00398564	0.0444627	intron-variant	NEB	GRCh38.p7	2:151577773	TAGTAAAGACAGGGT[A/T]TCACCATGTTGGTCA	4703
rs549826996	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	NEB, RIF1	GRCh38.p7	2:151485617	TTAAAACCCAAAGGA[C/G]AAAGGATGGTACTAC	4703
rs549830185	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151615625	ATATTGGCTGTTTCT[C/T]ACATATTATTTAAAG	4703
rs549838776	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151628416	GAGGTTTGTTTGGGA[A/T]TCCTCAAGTGAAAAA	4703
rs549857007	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151697714	TGATTATAACACTTA[C/T]ATTTTCTAACACTAA	4703
rs549867834	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151706674	ATTTCCCTGCCCATT[C/G]AATTAACCCCACAGA	4703
rs549878144	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151566200	TTTGATACATTTAGT[A/C]ACGTAGAAGTATGTG	4703
rs549888246	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151606717	TTGGTAGAGTTTCTA[C/T]AGAGGGAAAATAAAG	4703
rs549919581	snp	G/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151526524	GCTCAGATATGCCAT[G/T]TGTCCCTCCCATAAG	4703
rs549926192	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151729203	TCCCTGGTGGCAGAG[A/G]TGGTGTCCTACAAGT	4703
rs549927406	snp	C/T	0.00517822	0.0506191	intron-variant	NEB, RIF1	GRCh38.p7	2:151506017	GAATATGAGATGACT[C/T]TAGCCACTGTGTGGT	4703
rs549955221	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151645097	GACCACCGTCCTGTA[C/T]GTGTGCCTTTGTTGG	4703
rs549970489	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151664301	TACTTATTTTAACAA[A/G]ACTCAGTCACTACTT	4703
rs549971753	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151638109	GAGATAAATGCCAAT[C/T]TTTGAACAGAGATAA	4703
rs549981562	snp	A/T	0.0111196	0.0737302	intron-variant	NEB	GRCh38.p7	2:151572522	TTATATATATATATA[A/T]AATATATATATAAAA	4703
rs550008306	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151637440	AGTTGGACTGTGAAC[A/G]CCTCATTCTAAGAAG	4703
rs550039083	snp	G/T	1.65693e-05	0.00287826	intron-variant	NEB, RIF1	GRCh38.p7	2:151505586	CTGCAGATTTAAAAA[G/T]GGGAAAAGAAAGGTA	4703
rs550046486	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151734094	ATATAGGAACGTAGA[C/G]CAGCGTATCTTCTTT	4703
rs550047078	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151631912	CGATGTATTCTTCTA[C/T]ACATTTCAAAATATC	4703
rs550057953	snp	A/G	1.70842e-05	0.00292264	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151512781	AATGATCTCTGGAGT[A/G]TCAACCACAGAAGTG	4703
rs550078964	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151670870	TTCAAGATCCCAGTT[G/T]CCTCAAAAGGCAGCC	4703
rs550094523	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151636720	TGGGAGGCGGAAGTT[G/T]CAGTGAGCTGAGATT	4703
rs550100261	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151721342	TTGTCTGCCTTTCAA[A/G]GTCCTGCTGCCGGCA	4703
rs550107741	snp	A/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151578179	GGAAATAAATAACCT[A/T]CTGTAATCCATCATT	4703
rs550127171	in-del	-/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151509613	GGGGAGGAAGAGAGG[-/T]TTTTTTTTTTGTTTG	4703
rs550138461	snp	C/T	0	0	upstream-variant-2KB	NEB	GRCh38.p7	2:151736317	GTAAATTTCTAGAAA[C/T]AGAAATACTGAGGCA	4703
rs550142812	snp	A/C/G			intron-variant	NEB	GRCh38.p7	2:151726869	TACCTCTATGAAAAA[A/C/G]TAATTAGGAGATCCT	4703
rs550157545	snp	A/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151728233	AATAAACTATTTTTT[A/T]AAAACAGTTGAAAAT	4703
rs550158943	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151684323	ATCTGCAGAAAAAAC[C/T]GTTATAAATATTTAT	4703
rs550176368	snp	A/G	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151732324	CTAAAGGCAAGAGCC[A/G]GTGAGGAAAAACCGT	4703
rs550191566	snp	C/T	9.85885e-05	0.0070203	missense	NEB	GRCh38.p7	2:151562756	TGATTCATCATGTCA[C/T]TGGGGATATGAACAT	4703
rs550272381	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151581646	GTCAATTACCACATA[A/G]ATAAAATTATAAAGT	4703
rs550296441	snp	A/G	3.35357e-05	0.00409472	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151526186	TTGCTGACAGTCTTC[A/G]CCAGCAGGATCTGAG	4703
rs550314687	snp	G/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151497965	TTTTTTCATTTTTGT[G/T]AGTACGGTGCCTCCT	4703
rs550322123	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151690532	AAAATATTTATTTTT[A/G]TTATTGTCTAACACA	4703
rs550325427	snp	C/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151495081	TATCCTCTATGCTCT[C/G]CCTCTTGCTTTAGTT	4703
rs550329590	in-del	-/TAT	0.00517822	0.0506191	intron-variant	NEB	GRCh38.p7	2:151676621	TTCCTACTGCTGTTA[-/TAT]TATTGTTCATTCCTT	4703
rs550331661	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151532271	GGCCCCCAGAGGTTA[C/T]GAGACTGACCCAAGG	4703
rs550346485	snp	A/G	0.00119737	0.0244387	intron-variant	NEB, RIF1	GRCh38.p7	2:151531985	AAACACCAGAGTGGG[A/G]GATGGTATCTAGCTT	4703
rs550368508	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151661447	CTGCAACTGTTTCAC[A/G]TTTAGATCCAAATCA	4703
rs550369455	snp	C/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151566290	AGGCATCCCCTGGGT[C/G]CCAGCCAAACCTATT	4703
rs550390253	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151521690	AGAGGTATTTTTCAA[A/G]CAGCAATCCCATTGA	4703
rs550391834	snp	A/T	0.00199481	0.0315187	intron-variant	NEB, RIF1	GRCh38.p7	2:151515538	TTTTAAAAATCACTG[A/T]ATAGCTTAGGTGGGC	4703
rs550414166	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151573428	TGAGTGGGAAGAGGC[A/G]TCTATACTGCAGTGA	4703
rs550432268	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151707887	CTCCACAGAGCATCA[C/G]GACAGTATGCTACAG	4703
rs550442008	in-del	-/A	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151692988	AACAAAGAAGGAAAG[-/A]AAAAATGAGTTTAAG	4703
rs550447099	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151639139	TGACATTTATGATGG[C/T]GATTGAGAAATGCAA	4703
rs550447698	snp	C/G/T	0.00319074	0.0398324	intron-variant	NEB	GRCh38.p7	2:151676516	TCTTCTTACCTACCC[C/G/T]CTAATATCCAGACTC	4703
rs550452858	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151563510	ACGCTACTCCATTTC[C/T]CAGCTAACCTGAACC	4703
rs550456346	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151626698	TCTGCCACCATGCCC[A/G]GCTAATTTTTTGTAT	4703
rs550469336	snp	C/T	0.00597247	0.0543191	intron-variant	NEB	GRCh38.p7	2:151555267	TGTATCAAAAGTACT[C/T]TTAAACCACAGAGCG	4703
rs550482658	snp	A/G	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151628787	GAATCACTTGAACCC[A/G]GGAGGCGGAGGTTGC	4703
rs550493617	snp	C/T	1.65784e-05	0.00287905	missense, intron-variant	NEB	GRCh38.p7	2:151633698	CATGGATGACATCGC[C/T]CTGGTCAGGCAGGCA	4703
rs550494388	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151684666	GTCGTTTGCTTACAT[A/T]CATAGGACAATGCAG	4703
rs550498649	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151706272	GCTACATAAAATCCA[C/T]AAATGCTAGGAAAGC	4703
rs550501273	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151516251	GCTGTTGAAATAAGA[C/T]ATATGGTAAATATTT	4703
rs550520536	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151546099	GTGTAAGCTGAGCAG[A/G]GCTTTCATGTGTCCT	4703
rs550543287	snp	C/T	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151534935	ATTTAAGTAAATATA[C/T]CATTGGCTATATTTT	4703
rs550544634	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151624768	CATGTTTAAAAAATT[A/G]GTATCCTTCTTGAAT	4703
rs550556368	snp	A/C	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151639682	ACAATGACTAAATAT[A/C]AAAATATACATGATA	4703
rs550584748	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151560477	CCTGGACATGCCCAC[A/G]GGAGTGCTAGGGGTA	4703
rs550585111	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151566971	GATTGAAAGTTACTC[A/G]GAAATGCAGTCAGTA	4703
rs550589802	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151708119	CCTTCCACCTGCTCT[A/G]GGATATCACTCCAGA	4703
rs550591751	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151716709	TGCTTAAGATAAAAA[G/T]CTTGAGGTTTCATCA	4703
rs550600476	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151673844	GTTCACGCCATTCTC[C/G]GGCCTCAGCCTCCCT	4703
rs550607466	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151646763	CAAGTGATTCTGGTG[C/G]CTCAGCCACCTGAGT	4703
rs550608313	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151621575	GCAGGTACCAAAGAT[G/T]TAGGAGTCAAAACTG	4703
rs550614355	snp	C/T	0.00636936	0.0560724	intron-variant	NEB	GRCh38.p7	2:151558858	AACCCCAGAAGAAAA[C/T]CTAGGCAATACCTTT	4703
rs550620134	in-del	-/AG	0.00199481	0.0315187	intron-variant	NEB, RIF1	GRCh38.p7	2:151511790	ATCATGAGGGGAGTC[-/AG]GGGTTAGACTGTGTG	4703
rs550623411	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151573911	AAAATGACTTCTTCT[A/G]CAAATAATGATAATT	4703
rs550660975	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151679215	AATGACTTCAGTTCA[C/T]ATCTTGGTTAAAGAT	4703
rs550661724	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151616668	CACTGCACTCCAGCC[C/T]GGGTGACAGAGTGAA	4703
rs550671525	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151653768	AGAGCATCTTACTCT[A/G]ATGGATCTTAGAGGT	4703
rs550679734	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151543861	TATGCATTGCTTATG[C/T]TTCTTGGGACAACGT	4703
rs550715282	snp	C/T	8.2848e-05	0.00643561	missense, intron-variant	NEB	GRCh38.p7	2:151618363	GTTTCTGGACGCTGA[C/T]GGTAGATAGTATCAC	4703
rs550720877	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151667741	TTGCTATGTTGCCCA[C/G]GCTGGTCTTGAACTC	4703
rs550721502	snp	G/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151523101	TATAATGATATGACC[G/T]TGTACATTTAAAAAC	4703
rs550731190	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151546708	GGATTACAGGCGTAC[A/C]TCATCGTGCCTGGCT	4703
rs550743428	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151718145	GGCGTGAGCCACCGC[A/G]CCTGGCCAACTTCCT	4703
rs550752514	snp	A/T	0.110519	0.207473	intron-variant	NEB	GRCh38.p7	2:151722472	TGAAGTATCTTCTGA[A/T]AGCAAGAGCTCTTTG	4703
rs550794569	snp	A/C			missense	NEB	GRCh38.p7	2:151562770	ATTGGGGATATGAAC[A/C]TTTGCTTTGGTATCC	4703
rs550804983	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151724987	AATGCACAGTTAGAG[C/T]TCATGACAGGCATGT	4703
rs550832252	snp	A/G	8.38835e-05	0.0064757	synonymous-codon	NEB	GRCh38.p7	2:151672417	CTCAAGACTCATGGC[A/G]TCAGGTAGGTATGTG	4703
rs550849471	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151609688	TGTGAATGGTACCCC[C/T]AGCCCCACCCCCAGG	4703
rs550884017	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151570741	AGAGCATAGATGAGA[A/G]TCATTCTATGCACCA	4703
rs550889123	snp	A/C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151674421	CAATTTAAACAAGCA[A/C/T]TTGATTACTTTTCAA	4703
rs550913954	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151646004	CCACTAAATAAGGAA[G/T]CTAAGTCATATGTAG	4703
rs550925801	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151672781	GCTTTGTGACTTTCT[C/T]AAGAGTGTACAAAAA	4703
rs550926787	in-del	-/AG	0.00199481	0.0315187	intron-variant	NEB, RIF1	GRCh38.p7	2:151487092	ACTGACAGAAAAGAC[-/AG]AATATGCTGCTAATT	4703
rs550938736	snp	A/T	0.00279162	0.0372561	intron-variant	NEB	GRCh38.p7	2:151693295	AAGTTCAGGTGTACA[A/T]GTGCAGGATTGTGGG	4703
rs550944564	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151723261	ATTCTAGACATACTC[C/T]TCTGAAATACAACAT	4703
rs550973714	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151638408	CCGCAGCTTGGGATA[G/T]TGGATTTGAAGGTGA	4703
rs550979811	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151486990	ATGGTTGGAAAAAAA[A/G]CTTAAAATCATTGTA	4703
rs550991910	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151493971	AATCTATTACTATTA[A/G]TGAGAACACCTCTCA	4703
rs550993536	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151543602	TTGGAAGTAAATCTG[A/G]GACTAAAACCCAATT	4703
rs550995865	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151702463	CTAATGTTGACAGTG[A/G]GGTGTTAAAGTCTCC	4703
rs551014775	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151645270	AGCATCTAATTCTTC[C/T]AATGGGGAAAAATCA	4703
rs551019146	snp	C/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151487462	TTTGCATAAGTGGAA[C/G]ATTACTATAAATAAT	4703
rs551070692	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151507737	GTTACAGGGGTTTTC[A/G]CCATGAACCTTGCCA	4703
rs551098215	snp	A/C	0	0	intron-variant	NEB, RIF1	GRCh38.p7	2:151522107	TCCCATCAGGCTCAG[A/C]AATTGGGCCTATTAT	4703
rs551108095	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151730794	CCATTGTCAGTAGGC[C/T]GCCTGTGCTATTTCA	4703
rs551129164	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151509222	TCATCTAAATGGAAG[C/T]GAATTAAAGCCAGAT	4703
rs551129690	snp	A/G	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151631045	AAAAGGTAAAAATGC[A/G]ACCCCACGCCTTCAT	4703
rs551156819	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151535608	TTCCTGTCATTCTGT[A/G]TATTGGGCTTTAATT	4703
rs551166109	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151667062	AAATTAACTAAAATC[C/T]TGTTATGTAATTAAC	4703
rs551170885	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151643027	ATAAGAAGCACAATA[C/T]TTTAAAACCACATTA	4703
rs551181743	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151487653	TTTTCTTACACTATA[A/G]TGAGCATCCTACCGT	4703
rs551196688	snp	C/T	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151702906	TGAATTTGATCCTGT[C/T]ATTATGATGTTAGCT	4703
rs551216186	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151653912	TGAAAGGTAAAGACT[A/G]TCCATAAAAATAGTT	4703
rs551232956	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151528610	CATAAATATATGTCC[C/T]CTCTAGCACTAGTGG	4703
rs551234348	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151572521	TTTATATATATATAT[A/G]AAATATATATATAAA	4703
rs551253459	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151501787	AACTAATTGAAATTA[A/G]TATCCATGAGTTGTT	4703
rs551261559	snp	A/T	0.00638367	0.0561345	missense, intron-variant	NEB	GRCh38.p7	2:151617364	CAACAGTTTACTTAC[A/T]TCACTGTAGTTTATT	4703
rs551276462	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151617244	TGAGAACTATCTCTT[C/G]TACTGAAAATGGTAG	4703
rs551320985	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151552517	GGTTTCAGGAAACAA[C/T]AGCCAGCAGCATCTT	4703
rs551324977	in-del	-/TG			intron-variant	NEB	GRCh38.p7	2:151654589	GATTGAATGGATGTA[-/TG]TGTGTTAAAACTGGG	4703
rs551325251	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151509999	TTTTTCAGAGCTTAC[C/T]TTTTAAGCTATATGT	4703
rs551342717	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151659923	CAGTTCTCTGGTGAT[G/T]AATATTTAACTTATG	4703
rs551346638	snp	C/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151527237	CCCAGTCTTCCCCCA[C/G]ACTCTCCCCAGCCTC	4703
rs551346874	snp	C/G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151687008	AACTCATTACTAAAG[C/G/T]CAATGAAGAACGATA	4703
rs551363476	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151723862	CACATAGTTCAGGGC[A/T]ATATAGGACACTTGC	4703
rs551376268	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151680508	ACCTTTTCCTTAGAA[A/G]GAAATGTCAAATGGC	4703
rs551399063	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151573259	TTAATATCTTAATAA[A/C]GTTAATAATTTTACT	4703
rs551409341	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151653430	GAGTGAATCTATGAA[A/C]TTTAGATTGGATTTT	4703
rs551420257	snp	A/C			intron-variant	NEB, RIF1	GRCh38.p7	2:151488042	TTTTATTTTTATATT[A/C]CTGGTTACTAGTCAT	4703
rs551422314	in-del	-/TGTGTG			intron-variant	NEB	GRCh38.p7	2:151638834	GTGTGTGTGTGTGTG[-/TGTGTG]GGTTACCTGGTAGTA	4703
rs551432484	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151564302	TGGGATTACACGCAC[A/G]CACCACTATGCCTGG	4703
rs551433596	in-del	-/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151675746	TTTTGTTAGTTTCTA[-/T]TTTTTTATCCCTAGA	4703
rs551464446	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151571430	ATTGAGATAACTTTA[A/G]ACATTAATGGGTTAT	4703
rs551471949	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151571340	AATGATAGCCTTGAA[G/T]TAGTTGCTCATGCTT	4703
rs551514489	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151609158	GCAATTGGAGATTGC[A/G]CTCCAGCCTGGGCAA	4703
rs551517727	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151673693	CATGTAACAGTGAAC[A/T]CTGCAGGGCATGCAT	4703
rs551520922	in-del	-/A	0.000349502	0.0132147	intron-variant	NEB	GRCh38.p7	2:151659174	TGTAGAGATGCTAGG[-/A]AAAAAAACAGTGTAA	4703
rs551546597	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151535271	TTAGCGTAGCTCTTC[C/T]AACAACTGACATTTT	4703
rs551548208	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151553026	TGAAATCCTCATTAC[A/G]GTATTTAATTTGCGT	4703
rs551562850	snp	A/G	0.0792508	0.182605	intron-variant	NEB	GRCh38.p7	2:151617489	AAAAAAAAAAAAAAA[A/G]AGAGAGAGAGAGAGA	4703
rs551573518	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151685485	TGTTATTGACAGGAG[A/G]TAACCCCACTGAGAA	4703
rs551578623	snp	C/T	0.0134861	0.0810011	intron-variant	NEB	GRCh38.p7	2:151560775	AGCAGGTTTTCCTTC[C/T]GTGTCTGTCCTTCTC	4703
rs551589373	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151716978	GTTATGAGGTCCACT[A/G]CCCACTGCTGTTAAC	4703
rs551606658	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151731444	CTTCTCTGTTTTCTG[C/T]ATATTTTTAAAGCTA	4703
rs551610043	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151678410	GCTGTTTCTGCCTAT[C/T]CAAGTGAGGTTGAGA	4703
rs551640716	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151689822	CACAAAATATTAAGA[G/T]GCTCAGAAAAGTGGC	4703
rs551649582	snp	C/T	0.000488878	0.0156269	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151493361	AAAATACCGAGCTAA[C/T]GTTTTCTTGGTTGCG	4703
rs551656396	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151511681	TGACCATCACTGACA[A/G]TCGTTCATACAAGTG	4703
rs551668800	snp	A/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151566947	AGCAGATTTTTTTTA[A/T]AAAAATTTGATTGAA	4703
rs551670960	snp	C/G	0.0111196	0.0737302	intron-variant	NEB	GRCh38.p7	2:151559605	ACCATGGAATACTAT[C/G]CAGCCATAAAAAAGA	4703
rs551680049	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151680886	CTGAAGATTAATACG[C/T]CAAAATCCTTGAAAT	4703
rs551703465	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151686120	ATAAAGCAATATTGC[A/C]ACAGCAATAGGTGTG	4703
rs551705849	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151728349	TTTAATATTAACTTG[A/T]AAATGACTAAGGGAA	4703
rs551736548	snp	C/T	0.00279162	0.0372561	intron-variant	NEB	GRCh38.p7	2:151698870	GTCTCCATCTCTTTT[C/T]TTTTTTTTTTAATTA	4703
rs551745393	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151719261	GTCAATGACTGACAT[C/T]TCAATGTGTGTCTTA	4703
rs551782392	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151711233	ACTGAGACCATGATA[C/T]GCGGTTTTGAAATAC	4703
rs551789097	snp	A/C			intron-variant	NEB, RIF1	GRCh38.p7	2:151518532	GTCAAGATCAAACTA[A/C]AAATGGCAAACACTA	4703
rs551793348	snp	C/T	0.00279162	0.0372561	intron-variant	NEB, RIF1	GRCh38.p7	2:151499862	AGTATAGAGGTTCAA[C/T]ATGTGGCATTGTCTA	4703
rs551799555	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151708045	TCCCCTGTTATGCAG[A/G]TGAACTGTCAGGGCT	4703
rs551804427	snp	A/T	0.000399281	0.0141238	synonymous-codon	NEB	GRCh38.p7	2:151664852	CTTGTTCCATTTTTC[A/T]GTGTAGAGCCTCTGC	4703
rs551823879	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151557110	GATCAACAAAATAGA[C/T]AGACTGCTAGCAAGA	4703
rs551832094	snp	G/T	9.94102e-05	0.00704948	intron-variant	NEB, RIF1	GRCh38.p7	2:151506145	CAGAAAATATTGCAA[G/T]TGCATTCACTGTGTC	4703
rs551850470	snp	A/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151493682	TTAAAGATACACAAA[A/T]GTTTTGGAAAAACTG	4703
rs551850674	snp	A/C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151628049	TCATAAATAGTCTAA[A/C/T]AGCAACAGTCTAATG	4703
rs551861920	snp	A/G	1.67902e-05	0.00289738	intron-variant	NEB	GRCh38.p7	2:151568446	AATGAGAGGCAAGGG[A/G]GCAAGTTACTTGTTA	4703
rs551874737	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151726532	AGCCTCCAGAGGACA[C/T]GCAATCAAGCCACCC	4703
rs551880764	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151555130	AGACTTAATGGGAAA[A/T]ACCCGACTCTGAGAT	4703
rs551898907	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151513573	GACATCGAATAGTAG[C/T]ACTGACCTGACTGGC	4703
rs551916944	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151714806	AGGGAGAAAGAAGAT[A/G]TGATCCTGCTGCAAC	4703
rs551937560	snp	G/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151513097	GGGATCATCAACAGA[G/T]AGTAAGGCATGGATT	4703
rs551941569	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151637355	CTGTGGAGGGGAAGC[A/G]GAGGGGTGTTGAAGG	4703
rs552010760	in-del	-/C			intron-variant	NEB	GRCh38.p7	2:151546634	CAAGATCTTGGCTGA[-/C]TGCAACCTCCGCCTC	4703
rs552014509	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151707284	AACACATGGTCCTTG[C/T]CCTCAAAGAGAGAGA	4703
rs552015343	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151639695	ATCAAAATATACATG[A/G]TATATATCAGTTATT	4703
rs552019813	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151517754	TTGATACCTCTAAGC[A/G]TAGAAAAGGTACAGT	4703
rs552024643	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151567574	TATCAGCAAATTCAG[C/T]CCCCCAGCTTTTTGT	4703
rs552027767	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151533924	TTGCTTTTGCAACTC[A/G]ATCTGCAGTTTACAG	4703
rs552034750	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151607839	ATTGTTAAAATGAAG[C/T]TAACATTTAAATCAG	4703
rs552040955	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151653290	ATGCTAGCAATATGC[A/G]GAATATCTAAGTAAA	4703
rs552060376	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151542894	CTCCAACCCATGTTT[A/C]TATAATAGCTTCATT	4703
rs552067797	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151556479	GTGTTACAGAAAATG[C/T]TCCTGATTAAGAGAT	4703
rs552094328	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151658342	ATTAGGTTGTAAATA[C/T]ACTTTAAAAAATGTG	4703
rs552113061	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151619356	AAATTGTTTGAAATA[C/T]ACAAACAAATTGCAG	4703
rs552126147	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151705863	ACTTATAAGTGGAAG[C/G]TAAGCTATGAGGACA	4703
rs552133013	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151661207	TCTTGGCATCATTAT[C/T]CTGAAATGTTAATCA	4703
rs552134884	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151537737	CACTTAGCAATTGAG[C/T]TTTATGATTTAAACA	4703
rs552140238	snp	A/G	0.000399281	0.0141238	missense	NEB	GRCh38.p7	2:151665394	GTGTCCATGGCGTAA[A/G]TGAACTTCAGCTTCT	4703
rs552146632	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151547981	CAGATATGCAAACCA[A/G]TAGTTGGTGTAGAAA	4703
rs552168614	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151503961	AATCAGTTTATTTTT[C/T]AGGAAGAGCATCTTT	4703
rs552168697	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151668633	AGGCTAGTTACATAC[A/G]AAAAAAGATTTTGTG	4703
rs552182544	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151554551	GGCAACAGAGTGAGA[C/G]CTGTCTTAAAAAGAA	4703
rs552200908	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151725813	AAATACCCTAAAATG[A/G]TTCTTTCAATCTTTT	4703
rs552202257	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151694025	TACCTATACTTATGT[A/G]TATTAAGCTCGTTTC	4703
rs552207300	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151669188	ATAATATAAATTTCA[C/T]CAAGCAGAGACTCCT	4703
rs552212006	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151619952	ACCCCACAATGGTTC[A/C]TTTATATATGCTAGA	4703
rs552230672	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151655651	AAGGTCAAGAGAAGA[A/C]AAAAAATAAGAGATG	4703
rs552239683	snp	A/G	2.26549e-05	0.00336555	intron-variant	NEB	GRCh38.p7	2:151682789	AACACCAAGAGAAAG[A/G]TTACATTTCTTTGCT	4703
rs552252041	snp	C/T	0.000798403	0.0199641	intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151534509	TGAAGAAGGCTGGAG[C/T]GTGGGATAGGTCAGA	4703
rs552255524	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151717704	CAAGACTCATGGCCC[C/T]AGATCTGCTTTCTTC	4703
rs552265116	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151645736	AATGAGATTCTCCTG[C/T]GTGGGTTTTGTATGC	4703
rs552308369	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151546634	CAAGATCTTGGCTGA[A/C]TGCAACCTCCGCCTC	4703
rs552318393	snp	A/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151495535	CACAAGGTTGTTTGC[A/T]ACTGAAAGCTGAAGT	4703
rs552334918	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151581956	CATAATTTAAAATGA[G/T]TCAGAAATATGGTAG	4703
rs552335910	snp	C/T	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151634510	AGCCGGGCGTGGTGG[C/T]GGGCGCCTGTAGTCC	4703
rs552352912	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151709512	CTACTCTTTTTCAAA[A/T]GCCTCACATCCACTG	4703
rs552379239	snp	A/G	1.72958e-05	0.00294068	synonymous-codon	NEB	GRCh38.p7	2:151552708	TTTGACAGCCTGCAC[A/G]TAGACTGGTGTATCT	4703
rs552393379	in-del	-/AGTC	0.00119737	0.0244387	intron-variant	NEB, RIF1	GRCh38.p7	2:151501029	CTATATGTGGCTTCA[-/AGTC]AGTCCAGTATCTTTT	4703
rs552422028	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151540022	AGGATTTGAATCCAT[A/G]TCTGGCTGACTGCAA	4703
rs552439665	snp	C/T	0.000399281	0.0141238	missense	NEB	GRCh38.p7	2:151694420	TTGTTTTTTTCATAG[C/T]CTTTCTTGTACATCA	4703
rs552439882	snp	C/G	3.34158e-05	0.00408739	intron-variant	NEB, RIF1	GRCh38.p7	2:151490090	AAGCTGAAAAAAAGG[C/G]GGCAAATTCTTTATA	4703
rs552448949	snp	A/C	0.00716266	0.059414	intron-variant	NEB, RIF1	GRCh38.p7	2:151496564	TGCACCCTCTAGAGA[A/C]GCAGGGACCTCAGCT	4703
rs552455799	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151682043	TTACTTTTGTACCAA[A/C]CTAATAAATCCATAC	4703
rs552459382	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151538980	TGACTTTGTAATTTT[C/G]TTTTTTAGATGGATC	4703
rs552465899	snp	C/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151525561	GGGACTCATATAATA[C/G]CAAGGTTACTACAGC	4703
rs552504401	snp	A/C	0.00119737	0.0244387	intron-variant	NEB, RIF1	GRCh38.p7	2:151504624	CAGTCCTCCATTGAC[A/C]AGGGGAATCCCAAGA	4703
rs552505883	in-del	-/ATT	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151689915	GAGCTAATTTGTGTC[-/ATT]AAAATATATTTTATA	4703
rs552515107	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151725272	TAAGCCAAGCTTTTA[A/G]AAGTTTCTTTGGGTT	4703
rs552515749	snp	C/T	0.000698347	0.0186731	intron-variant	NEB	GRCh38.p7	2:151618227	TCAGAATTTTTAAAT[C/T]GTTCTGTGGTAACTT	4703
rs552522048	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151682311	TAAAACTTGTCAAAG[C/T]GTACACTTAATGTGA	4703
rs552538657	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151575561	CTCACTCCTAGTCAA[A/G]GGGTGACCACAAGGA	4703
rs552552295	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151617679	TGAAAAGTATAATTG[A/G]ATTGAAGTATTTAAA	4703
rs552566305	in-del	-/TCTC	0.00159617	0.0282053	intron-variant	NEB, RIF1	GRCh38.p7	2:151529558	TTTTTTTTAACAGAT[-/TCTC]TCTCTGTCACCCAGG	4703
rs552579849	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151704558	TGCAGGATATAATCT[C/T]GTGGTGCGCCGTTTT	4703
rs552598372	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151545744	TGCTTAGACATAGTA[A/G]CCATTCCACAGTTAA	4703
rs552601131	snp	A/G	0.00358779	0.0422022	intron-variant	NEB	GRCh38.p7	2:151574167	TTTTAGTAGAGACAG[A/G]GTTTCACCGTGTTAG	4703
rs552610311	snp	A/G	0.00795532	0.062565	intron-variant	NEB	GRCh38.p7	2:151724490	GGTTACTAGGAAAAC[A/G]TTGACCATGCCAACA	4703
rs552640559	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151710203	GTCTTACCATAATGT[A/G]TTGTAAAAATTGAGG	4703
rs552657693	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151660245	ACTGTTCAACTTCTC[C/T]TCCGGCCTAGTCCTT	4703
rs552686980	snp	A/G	8.30668e-05	0.00644411	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151610516	ATGGAAGGTACTCAC[A/G]TCACTGGCGATGTCC	4703
rs552701643	snp	C/T			intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151507423	CTTCTCTGTTTTTTC[C/T]TGAAGCAGATAATAA	4703
rs552717386	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151563283	GCCTCCAAAGTGCTG[A/G]GATTACAGGTGTGAG	4703
rs552720477	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151642931	GACACATGCAGACAG[C/T]CTGATTTTTAATGAG	4703
rs552727689	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151618081	ACAAAACAAACAAAC[A/T]AAAGCACACAGTACT	4703
rs552734719	snp	A/C	1.68026e-05	0.00289845	intron-variant	NEB, RIF1	GRCh38.p7	2:151524274	GTCTTTTATAATCTC[A/C]TCACATGAGAGCCAC	4703
rs552753865	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151717183	CTGTTTTCAAAAGGT[A/G]ATTTTCACATTTATC	4703
rs552774805	snp	C/T	1.65597e-05	0.00287743	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151633798	CACCCCCAGCATGTC[C/T]ACTGGGCTGCTGAAC	4703
rs552789987	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151647599	GCCTCCTGATATGAG[A/G]TACTGAGGAGGACAC	4703
rs552806247	snp	G/T	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151574945	GGGTCTCCCTATGTT[G/T]CCCAGACTAGTCTTG	4703
rs552817361	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151666550	AAAATAAACAATTAG[C/G]AAAATATTTTTAATG	4703
rs552826360	in-del	-/G	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151625908	TGTGTTTGGTAACCA[-/G]GTCACTCTCACCCCA	4703
rs552843115	snp	A/G	0.000182	0.00953766	intron-variant	NEB	GRCh38.p7	2:151591325	GTTAGTGTTTGTTCC[A/G]GTTGGGAAGGAGGAG	4703
rs552844692	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151488750	TGCTTTGAGATGGGT[A/G]TCTAATTTTATTATT	4703
rs552847899	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151591861	AACAAACATTGAGAT[A/G]TACATTACACAGACA	4703
rs552854544	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151618571	AAACACAAAAATACC[A/G]ATGAATAGTTAAGGT	4703
rs552856891	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151531734	AATTTAAAATGCCCC[C/T]CCATGTTTGCAGATG	4703
rs552856923	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151488209	TTAATATTTTTGTTA[C/T]GTATGCTGTAAATGT	4703
rs552857196	snp	C/T	0.00119737	0.0244387	intron-variant	NEB, RIF1	GRCh38.p7	2:151495159	ATATCACTATCATGG[C/T]GAATCAGTGGAAAAT	4703
rs552874566	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151530578	CTTTAGGAGAAAGTC[A/G]TGGAAATTCATTTTT	4703
rs552878499	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151640230	GATTAAAATTCCTGT[C/T]GATAAAGGCAATGCT	4703
rs552917581	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151616427	GGCGTGGTGGCTCAC[A/G]CCTGTAATCCCAGCA	4703
rs552931809	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151687941	CTACTCTTTTTAATG[C/T]TCTGTAAACTTTCTA	4703
rs552968660	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151667305	TCCAAATAAAAAGTG[A/G]TTTTTAAGTTCATAA	4703
rs553020641	in-del	-/TAAAG	0.00392535	0.0441278	intron-variant	NEB	GRCh38.p7	2:151680055	GCATAAACAAACAAA[-/TAAAG]TAGAAAGAAAATTTA	4703
rs553022931	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151698446	GAGGTTTATGGTTGG[A/G]GGGATTAAAAAAAAT	4703
rs553041442	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151578619	TGAGCTGAGACTCCA[A/G]CCAGGGCCACAGGGC	4703
rs553043135	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151559898	TACCTATGTAATAAA[C/T]CTCCACGTTCTGCAC	4703
rs553055781	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151646812	GTGCCACCATACCCG[C/G]CTAATTTTTGTATTT	4703
rs553059981	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151699262	TAATCCAGTCTATCA[C/T]TGTTGGACATTTGGG	4703
rs553074727	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151563553	ATAAACAGGCAGACA[C/T]GGCAGCACACTTATG	4703
rs553079055	snp	C/T	0.000259374	0.0113851	missense	NEB	GRCh38.p7	2:151552707	TTTTGACAGCCTGCA[C/T]GTAGACTGGTGTATC	4703
rs553081790	in-del	-/ATTT			intron-variant	NEB	GRCh38.p7	2:151574746	TTTATTTATTTATTT[-/ATTT]GAGACAGGGTCTTGC	4703
rs553097509	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151673176	AAGGACCTGCTGTGG[G/T]GTTTTCCCATCAATA	4703
rs553159145	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151574448	TTTGAGATTTATTTT[A/T]CAGTCATGTTGAGAA	4703
rs553187006	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151486552	ATAATTTGTACATCC[A/G]TGTCCGTAGCAGCAT	4703
rs553190163	snp	C/T	3.45566e-05	0.00415658	intron-variant	NEB	GRCh38.p7	2:151537123	CCAATTCTCCTTGAG[C/T]ATATATACCTTGCTG	4703
rs553222973	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151583823	AATGTATTAAGAGGG[G/T]TTTTCTAATTTAAAT	4703
rs553228974	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151715368	AGATCCAGTGTCTAT[C/T]TCTCACATATTGGAC	4703
rs553229607	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151693349	CCATGGTGGTTTGCT[A/G]CACAGATCATCCTGT	4703
rs553268247	snp	C/T	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151572797	TCAAGTGATCCACCC[C/T]CCTCAGCCTCCCAAA	4703
rs553277624	snp	C/G	0.00755907	0.0610114	intron-variant	NEB	GRCh38.p7	2:151704214	AGGAGGCAGTCTGCC[C/G]GTTCTCAGATCTCCA	4703
rs553292905	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151730521	TCCTGTCCTTAGCCT[C/T]ACCCTGCTCTGTAGG	4703
rs553314467	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151704603	AAAGCGCAATATTCG[A/G]GAGGGAGTGACCCGA	4703
rs553314919	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151528758	CAAGAAGAGAGTCAA[C/T]GCAGGGAATATCTGA	4703
rs553336450	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151559377	CCATTGTGGAAGACA[C/G]TGTGGTGATTCCTCA	4703
rs553353710	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151534845	CTGGCAGTAATTCTT[C/G]AGGGTTGTCCAGTCT	4703
rs553363896	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151487067	TGTGTGCGCATGTGC[A/G]TGTGTGTGTACTGAC	4703
rs553367472	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151686511	TAGTAATATAAGTGA[C/G]CACTATATACTGACA	4703
rs553375465	snp	C/T	0.000122222	0.0078164	missense	NEB	GRCh38.p7	2:151565722	TTTGCGTACCTGACT[C/T]ATCATTTCCTGGTTC	4703
rs553375987	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151616622	TTGCTTGAACCCAGG[A/G]GGCGGAGGTTGCAGT	4703
rs553384058	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151511151	GTCAAAAGCAGAAGG[C/T]AAAAGGCTGGTGAGG	4703
rs553396871	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151503843	AGGATACTCTATTCC[C/T]TCAGGCTTATTGAGA	4703
rs553413475	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151540198	AGTATTGTTTGGGCA[C/T]TTTTTTTTCTCTTTA	4703
rs553416014	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151645592	ATCTGTCAGTCCTTC[A/G]TGGAACTACTTTAAT	4703
rs553439048	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151638514	TGCAGCTTCAGAGGA[A/C]TATGTGAGTTTACAG	4703
rs553445006	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151576454	TGTGTATATATTATA[C/T]ATACAACATAAAATA	4703
rs553452164	snp	C/T	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151696387	TGAATGCGGTTTTGT[C/T]TGACTCTAGAACTCA	4703
rs553463857	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151616744	TTGTCATCATAATAT[A/G]AAAGACACAGCATCT	4703
rs553472039	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151659388	TGCAACCTCCACCTC[C/G]CAGGCTCAAACAATC	4703
rs553486564	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151680574	ATATATGAATTAGGC[A/G]TGCTTTATTAATGAA	4703
rs553492759	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151720814	CTGCCCTTGGCCATG[C/T]ACTCTTCTGCTTCCC	4703
rs553507212	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151632162	CTCACTTTATTAAAA[A/T]ATTTTTTTTTGCTGA	4703
rs553510261	snp	G/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151493596	TAGGAAGCAAAAGTT[G/T]AAGAAAGAAGTAAAA	4703
rs553513895	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151510335	TTAAGGCCCAGGAAA[A/G]GCCTAGCCGAAACTT	4703
rs553527829	snp	C/T	1.66222e-05	0.00288285	missense	NEB	GRCh38.p7	2:151727834	CTGGCTGTGCCAGAG[C/T]TGGTTTGGAAGTTTC	4703
rs553542892	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151652255	TTTTGAGATACCGTC[C/T]GGCTCTGTTGCCCAG	4703
rs553561600	snp	A/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151705361	CATGTTTAATATTTT[A/T]ATATTCCTGTCTTTA	4703
rs553573261	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151515688	TTTGTAATTTTGTTA[C/T]TTTAATAGAATTTTA	4703
rs553578005	snp	A/C	0.00119737	0.0244387	missense, intron-variant	NEB	GRCh38.p7	2:151604577	CGCTCTGCAGGTCGT[A/C]GGCTTTCTTGGCCTG	4703
rs553585911	snp	C/G/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151531542	GGCTGGTCTCAAACT[C/G/T]GTGGCCTCAAGTGAT	4703
rs553595417	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151562898	TATTTCCCATATAGA[G/T]CAGTATCTCTAGAAT	4703
rs553610068	snp	C/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151523251	ATTTATAATAAAATA[C/T]GTTACATAGGAATTT	4703
rs553626030	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151656683	TTCTTATTACTCTCC[C/T]CATTTTATAGATGAA	4703
rs553630698	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151569979	TTAAATTCTTGGTGA[C/T]ATGAAGTCGTAAAAT	4703
rs553632770	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151562530	CAGGGACAACGGGAG[A/C]ATGGCAGCCAGGGTT	4703
rs553667593	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151569470	ACAATGTAAATGCTA[C/T]ATAAGCCAAGGAGGA	4703
rs553688128	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151727199	TAAGGTATAGCCAAA[C/T]ATTCAGATCCTCAAT	4703
rs553695316	snp	A/G	1.69861e-05	0.00291424	missense, intron-variant	NEB	GRCh38.p7	2:151636264	GCCTTGGCCGCCACG[A/G]TGGGGATGGCGTCGC	4703
rs553733560	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151734220	TTGACTCTAATCACA[C/T]ACGGTACATAGCAGA	4703
rs553757153	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151517276	TTCTGGAAAAACAGG[C/T]GAAGACCCTCATGCA	4703
rs553780822	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151649518	AATTACAGATTTCAG[A/G]GCACATACTTCAGTA	4703
rs553780946	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151575591	AGTCTTCCCCTGTTG[C/T]GGGAAGTCAGGGACC	4703
rs553797693	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151684452	TGTTTATTGAGAACT[C/T]ACCAGGGCCTGGCAC	4703
rs553807201	in-del	-/TC	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151612908	AAGTCACAGAGTACA[-/TC]TCTCTTTACTCATAT	4703
rs553823470	snp	G/T	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151576045	TTACTTAATAAAATT[G/T]TTGTTATTAATAAAG	4703
rs553824237	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	NEB	GRCh38.p7	2:151734778	ATGACTTTGAGAGGC[G/T]TTAACCCTTCCGTGA	4703
rs553827525	in-del	-/AAC			intron-variant	NEB	GRCh38.p7	2:151559107	AAGAAAAAAACAAAC[-/AAC]CCCATCAAAAAGTAG	4703
rs553835395	snp	C/T	0.00358779	0.0422022	intron-variant	NEB	GRCh38.p7	2:151626615	GATCTCAGCTCACTA[C/T]GAGCTCCGCCTCTCA	4703
rs553850451	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151550031	TCAACACTTTGGGAG[C/G]CCAAGGCAGGAGGAT	4703
rs553854859	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151634642	AAGACTCCATCTCAA[A/T]AAAATAAAATAAAAT	4703
rs553886802	snp	A/G	0.0023933	0.0345097	intron-variant	NEB, RIF1	GRCh38.p7	2:151505110	TATGTTATACTACTT[A/G]TATGTTTATATGTAT	4703
rs553893593	snp	G/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151516616	GTCAATTCCTAGACA[G/T]CAGTTTAAGGATAGT	4703
rs553895313	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151696592	ATAGAGTTATGAAAT[A/G]TTATCCCTCATAATT	4703
rs553897657	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151640783	AATATGTAAATTATA[G/T]GATAGATGTAGAAAC	4703
rs553901242	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151490955	AAATTGCACATGTCA[A/G]AATGCAACCATGGAT	4703
rs553939421	snp	C/G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151539590	TCTAGGGGTGTGGCT[C/G/T]TGGTAATGGGTACAG	4703
rs553955087	snp	C/T			upstream-variant-2KB	NEB	GRCh38.p7	2:151735384	TTCTTGCACTTTCTT[C/T]GCTCCTGAAGTATTT	4703
rs553984889	in-del	-/G	0.00438332	0.0466095	intron-variant	NEB	GRCh38.p7	2:151705951	GAGTGAGGGAGTAAA[-/G]ACTACATATTGATCA	4703
rs554012622	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151683989	AATACTGTATGACTT[C/T]ACATATATGAGGTAT	4703
rs554018092	snp	A/G	5.11295e-05	0.0050559	intron-variant	NEB, RIF1	GRCh38.p7	2:151519814	CCTGGACATCAATCA[A/G]TTTGGGAATTGGGGA	4703
rs554019582	snp	A/C	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151525031	CCTTAAACCCAAACC[A/C]ATTCTCGCCACTAAC	4703
rs554040025	snp	A/G	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151496703	GTTATCCACACAAAC[A/G]GAAAAACTCATTTTT	4703
rs554046143	snp	C/T	1.65603e-05	0.00287747	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151496348	AGGAGTTCCCTTGCC[C/T]ATGTTTTCTTTGTAT	4703
rs554049565	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151676112	ATCCTTATTTCCAAG[C/G]CATGACTATATGGAA	4703
rs554073356	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151663336	AATCCAACAATGCTC[C/T]CAGCAACAATAGTAG	4703
rs554075543	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151668872	GCAAAATTTTATTGC[C/T]GCCCCCTAGGCTCAT	4703
rs554082474	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151635473	GCACTTTGGGAGCCT[A/G]AGGCAAGTGGATCAC	4703
rs554096247	snp	G/T	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151594802	GTTTCCCTGACAAGT[G/T]CAACATTAGGTCAAA	4703
rs554104620	in-del	-/A			intron-variant	NEB	GRCh38.p7	2:151633526	AAGCAATAAAATTGT[-/A]TTCTGATTTAAATCT	4703
rs554106678	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151510226	CCAATAAACTTGTTT[A/G]TGGAGGCCTGGGGAG	4703
rs554107791	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151712309	TATTCTTAATGAGGT[C/G]TAAATGTTGGGCATT	4703
rs554120506	in-del	-/GTTGGTTTGTT	0.00119737	0.0244387	intron-variant	NEB, RIF1	GRCh38.p7	2:151493629	CTGTGACCTCGTGGG[-/GTTGGTTTGTT]GTTGGTTTGTTGTTT	4703
rs554150754	snp	A/G	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151504199	CTGGTGTATTAGTGC[A/G]TGGCGTGGGGAGCAA	4703
rs554175385	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151636121	CCTACACAAATATAT[A/C]AGGATATATTTTCAA	4703
rs554182078	in-del	-/TGTT	0.00398564	0.0444627	intron-variant, utr-variant-3-prime, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151498005	ATGAGGATTTGAGAC[-/TGTT]TGTTAGAACTCGGTG	4703
rs554194312	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151547399	CGTCTTGGTAAGACT[A/G]CTCCAGAAAGACCCC	4703
rs554212770	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151711300	CCAACCCCAAACCTG[A/G]GTCCATGAGCTAGAG	4703
rs554223659	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151718605	CCACCCCTTCCCTGG[C/T]TCAGAGGAGAAACAT	4703
rs554223924	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151726092	TGCTTTAATGATAAT[A/G]TGCATAATTTATCAT	4703
rs554231162	snp	A/G	0.000644004	0.0179329	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151592075	TGGATTGCAGCATCA[A/G]GGGAGTGTCAGCTGG	4703
rs554237986	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151665176	CACTATGAAAGAGAA[C/T]GCTCTAAACATAATG	4703
rs554251472	snp	A/C	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151704823	ATCACCCGTCTTCTG[A/C]GTCGCTCGCTCACGC	4703
rs554253941	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151682289	CTGCACAATTATATG[A/G]ATTTATTAAAACTTG	4703
rs554287308	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151567965	GCCAGGTCTGCCACA[C/T]TGAAACTGAACACCT	4703
rs554303939	snp	A/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151490281	GGATGAAAAATTTTT[A/T]AATTTGTTTTTGTAC	4703
rs554311072	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151662956	CATTCCCAAAGAGAA[A/G]TGTAGCCTTGCTTTC	4703
rs554323365	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151609577	TCTAGCATAATAGCA[A/G]CAATTATTTTAAAAA	4703
rs554323969	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151575255	TTGCTGTATGTTTTT[C/T]GGTTTTTTCTCCTTG	4703
rs554325054	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151734184	CAATTCAGTCAAGCA[A/G]TAAATTGGTTAGCAA	4703
rs554335343	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151645701	TCAGGAGATTATGCT[A/G]CAATGATAATGACAA	4703
rs554338455	in-del	-/AGAA	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151535157	AAGGCTGGATAAAAT[-/AGAA]AGAAAAAATTTGGGT	4703
rs554349461	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151574262	TACAGGCGTGAGCCA[C/T]CGCGCCAGGCATGTT	4703
rs554357395	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151612121	ATCCTTAGGGAATTT[C/T]CTACTTTATGAGCCA	4703
rs554366790	snp	C/T	4.97715e-05	0.00498831	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151612228	TGCTAGGACAATTTC[C/T]GGAGTGTCGGTAATG	4703
rs554367263	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151668735	CAGACTAGGCACTCT[C/T]GTGTTTTCCAATCTT	4703
rs554368027	snp	A/G	0.00279162	0.0372561	intron-variant	NEB	GRCh38.p7	2:151727035	CCAGCCTGGGCTACA[A/G]AGAAAGATTCTGTTT	4703
rs554404343	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151662726	CCAAGTCCCCTTGGT[C/T]AACAGATGACTATGG	4703
rs554417448	in-del	-/GG	0.00835141	0.0640778	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151498527	ATCTTCAAAAGCAAA[-/GG]GGAATGCAGGAAAGA	4703
rs554420915	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151576395	CAGGGTTTGTGTTTT[G/T]TTGTGTATGTGTGTG	4703
rs554445168	snp	G/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151635433	GAGCTATTGCTAAGA[G/T]TGTGACCTCACGCTT	4703
rs554455877	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151575938	CTGGAATCTTTTCAC[C/G]TAAGTTACTCAAATT	4703
rs554456375	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151554189	CCAAGGGAAATTTTT[A/T]AAAAATAAAGCATTA	4703
rs554458808	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151719332	TCTTTCTAATCTTCC[A/G]TGACACAACTGTGAA	4703
rs554485389	snp	C/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151496066	TAGGAAAATCTGTTA[C/T]TTCTTGATATTAGAA	4703
rs554488430	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151733636	CCCTGATCCACTGTT[C/T]GCAATATATCTTAGG	4703
rs554493195	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151503627	AATAGTAAAAATTTT[C/T]ACTACTTTGAAAACT	4703
rs554506351	snp	A/G	5.00154e-05	0.00500052	intron-variant	NEB	GRCh38.p7	2:151569417	CAACCCTGGTCATGT[A/G]GTCCTAGTTAGCCTA	4703
rs554538840	in-del	-/CT			intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151507472	AAGCAGGCAATAAGC[-/CT]CTCCTTCCAGAAGGG	4703
rs554540673	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151619175	ATATATTTTTAAGGG[C/T]TAAGTTTCATCTGAT	4703
rs554545811	snp	G/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151524116	AAATGGTAAAGTGGA[G/T]AACAAGAAAGGTCTA	4703
rs554577431	snp	C/T	0.000399281	0.0141238	missense	NEB	GRCh38.p7	2:151655830	ACCTTGTTCATGGTA[C/T]GTGCATTCTGCTTGG	4703
rs554584242	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151550136	GCCAGGCATGGTGGC[G/T]TGTACCTGTAGTCCC	4703
rs554588837	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151681529	GCATCATCACTCTTT[C/T]GGCTTCAGACTTCTA	4703
rs554593132	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151695818	TTGGGTAGGCCATCT[A/G]CATTACTGATCCTGT	4703
rs554603516	snp	A/G			synonymous-codon, intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151499373	AATCCCTTTTCCAAC[A/G]TTTTCTTTATACAAC	4703
rs554622262	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151530717	ATAGCCCAGCTCCCA[A/G]CCCGCAGCCATCACC	4703
rs554646451	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151661975	CTAGTTAGAAATAAT[C/T]CCTATTCTTTTTTTT	4703
rs554648466	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151489652	TCCTCCTGCATCAGC[A/G]TCCCAAAGTGCTGGC	4703
rs554675179	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151611634	GGATAAAAATAGATT[A/G]ATAAAATTTTGGATG	4703
rs554685729	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151724725	AGCCTCCTTGATGAA[C/T]ACAGGTATTGAACTC	4703
rs554715984	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151511083	AGAGCAAGTGACGTG[A/G]TCCCACACTGGGATA	4703
rs554733664	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151546994	GATTGGAGAAAAGAA[C/G]AGATTGAATGGATTG	4703
rs554741684	snp	A/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151655188	ATTGCTTCAACATTT[A/T]TATCAGTATTTACTG	4703
rs554762224	snp	C/T	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151710991	CAACTTGCAGGCTAA[C/T]GAATAGATCTTCGCC	4703
rs554767843	snp	A/G	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151488660	CTAAAAATAAAAAAA[A/G]AGTATTCTGTATTAT	4703
rs554776846	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151710757	AAAGAGGGTACTAAC[A/G]CCCCCTCCCCTTGCT	4703
rs554779217	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151573786	TGCGATCCATGAAAA[C/T]GGTATCTTCCTTGAA	4703
rs554797755	snp	C/T	0.00279162	0.0372561	intron-variant	NEB	GRCh38.p7	2:151562017	GAGCCTACACTGTTA[C/T]AGCAACTTTCTTTGC	4703
rs554800005	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151641638	GCCTGACCTATACAC[A/G]TGATTTTTAATGACA	4703
rs554809115	snp	A/G	4.08113e-05	0.00451708	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151526239	GGTTCCTCTTTCCTT[A/G]ACATGTTTCTCTTTG	4703
rs554825950	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151674128	TTTCAATCTTTTTAA[A/T]ACAATTATAATGCAG	4703
rs554830380	snp	C/T	0.00358779	0.0422022	intron-variant	NEB	GRCh38.p7	2:151689532	TTAAATTATTAAACA[C/T]AGAACTTTATTTAAA	4703
rs554915141	snp	C/G	1.73972e-05	0.00294929	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151516505	GTGATGTACGTTGGT[C/G]TTTCAAAGTCCAGCA	4703
rs554950818	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151649404	TATAGCATATTACAT[A/G]TAGTATATATATTCA	4703
rs554964408	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151640168	ATTTAGTTTGGTGGA[C/T]GGGCCAGGTATCACA	4703
rs554975445	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151567913	CATGGAAGAAAGACC[A/G]AAAAGTGAGCAGGTA	4703
rs554981365	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151633219	GTGTCTGTGAAACAG[C/T]CCAGTAGTGTACAGA	4703
rs554984749	snp	A/G	6.62449e-05	0.00575483	missense	NEB	GRCh38.p7	2:151671060	TGCTGAGCCAACACC[A/G]TGCCCATGGAATCAG	4703
rs555005834	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151617575	TCTTGTATACAAGGT[A/G]GAAATAAAATTATTA	4703
rs555018349	snp	C/T	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151562990	ACTTTAATATATTCT[C/T]CTTCTTTTGAAATTT	4703
rs555038381	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151636591	TCGAGACCAGCATGG[C/T]CAACATGGTGAAACC	4703
rs555046947	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151708949	AAACACCGTCTTACA[C/T]GTGGATGCTGTAATA	4703
rs555054057	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151687801	TAAAAAAATAAAAAC[A/G]TATTGAAAATTTGTG	4703
rs555082157	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151637012	CTTAACTGTTGATCA[C/T]GGCAATCAATTCAAC	4703
rs555083986	snp	A/C	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151527340	AGCTCGCCTATCGCT[A/C]CCCCAACCATCCTCC	4703
rs555087411	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151574390	TCATTTTAATCCTGA[C/T]ATGAATGAGAAGTTT	4703
rs555092927	snp	A/C	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151646890	CCCCACCTCAGCCTC[A/C]CAAAGTGCTGGGATT	4703
rs555111768	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151619059	AGTATAAAATGTAAA[G/T]TAAAGTAATTTAGCA	4703
rs555124282	snp	A/G	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151583191	CTATGCAAAGGTAAC[A/G]GCTCAGAGCAGCTGC	4703
rs555139925	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151718467	CCCTACTCTCAGGGG[A/C]CAGTCTAAAACCCCA	4703
rs555141104	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151543054	CTCCAAGAGTCCATG[C/T]TGTCTTGACTGTTCC	4703
rs555142334	in-del	-/T	0.00119737	0.0244387	intron-variant	NEB, RIF1	GRCh38.p7	2:151530103	TAAGGGCAAAAACTG[-/T]TTATCATCCATCATC	4703
rs555168193	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151724812	ACAATGCAGAGGTGA[C/T]GCACATGCTACTGAG	4703
rs555177762	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151707622	AAGTTGAGGGGTGTT[A/G]GGGGAGAATAGGGAA	4703
rs555177933	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151551033	AGTGCAGTGGTGCAA[C/T]CTCAGCTCACTGCAA	4703
rs555201508	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151725304	ACATTTACAGCAACA[A/T]GATCTATGGTTCATG	4703
rs555216853	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151550294	AAAAAAAAAAAACAC[G/T]AATTCCTCTGTGCTT	4703
rs555237537	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151665017	GCCAAGTAAACTAAA[C/T]ACACAATAAGAAAAA	4703
rs555253918	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151572583	CAGAGTCTCGCTCTG[C/T]CACCCAAGCTGGAGT	4703
rs555270787	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151715438	CAAATTCATATGTTG[A/G]AGACCTAACTCACAA	4703
rs555271841	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151671932	CCTGGTTAATTTTAG[A/G]TGACTCATTACAGAG	4703
rs555272619	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151658762	TCTAGGACTCTCATT[G/T]CCTTTTTCTCTTCTC	4703
rs555299523	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151685620	GAGCCATTAAAATAA[C/T]GTTGGCCCTTCCGTA	4703
rs555310415	snp	A/G			missense, intron-variant	NEB	GRCh38.p7	2:151609933	TGACATTTCTTGGCC[A/G]GCAAGATGCTTAACA	4703
rs555313113	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	NEB, RIF1	GRCh38.p7	2:151497554	AAAGTAGGATTAATA[C/T]GTATTATTTTAAATC	4703
rs555320115	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151637506	CAAAAAGTTCTCTTC[C/T]TTTTAACATCAGAGG	4703
rs555321675	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151518474	GAAGCTGCTCAGCAT[C/T]CCTATTTTTCCTCTT	4703
rs555335217	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151722234	CTGAAGACTGGAGTA[A/G]CAGTCTGGATTTTCA	4703
rs555346186	snp	A/C	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151629079	ATAATTTTCCAAAAA[A/C]AAATGAGTTGGCAAA	4703
rs555360650	snp	G/T	0.00676609	0.0577691	intron-variant	NEB	GRCh38.p7	2:151546910	CAAATAAGTCATGTT[G/T]TTTTTCATTTAAGTC	4703
rs555373555	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151655053	CAAGCACAATGAACA[A/C]AGAGATAAACAGACA	4703
rs555385718	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151728697	AAAATAATGCATGTA[A/T]GAAAAAAAGATAAGC	4703
rs555419306	snp	C/T	0.00199481	0.0315187	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151506369	AGACACTAGACGATG[C/T]TCCCAGGCAAGTGCC	4703
rs555424690	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151725934	TGCTAATACAATGCA[A/G]AAATATTCAATTCAG	4703
rs555435863	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151635620	CTGAGGCAGGAGAAT[C/T]GCTTGACCCCAGGGG	4703
rs555436960	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151651449	TAATCCATTAAATAG[C/T]AGGATCTTTTTGTGG	4703
rs555445835	in-del	-/AG			frameshift-variant, intron-variant	NEB, RIF1	GRCh38.p7	2:151494212	CATCTCAGGAGTGAC[-/AG]GGGTTGCGGTGGCTT	4703
rs555479550	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151628395	TGTTGGAGATCAAAT[C/T]TGACTGAGGTTTGTT	4703
rs555509949	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151664103	GTAAATAAATTGGTT[C/T]AGAGAGATTTAGAAA	4703
rs555514418	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151657929	AGAACTCAGCCCTTA[C/T]TATTTCGGTTCCTTA	4703
rs555516831	snp	A/G	0.000221865	0.0105301	synonymous-codon	NEB	GRCh38.p7	2:151570096	ATCGCTCTGCAGTTC[A/G]TAGGCCTTCTTGGCC	4703
rs555516873	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151577846	GCCTCCCCAAAGTGC[C/T]GAGATTACAGGTGTG	4703
rs555547035	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	NEB	GRCh38.p7	2:151735698	AGGCCAGGAGTTTGA[A/G]AAAGTAATCTCATAT	4703
rs555564051	snp	C/G	0.0023933	0.0345097	intron-variant	NEB, RIF1	GRCh38.p7	2:151505037	GGGAATCCTATCATT[C/G]ATATGATGTGTCATA	4703
rs555573061	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151716003	TTTTAAAATAGACTT[C/T]AAATAAACATTTAAA	4703
rs555573858	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151657122	CTCCTTTTGGGGTTG[C/T]GTGTGCAAGTTGGGG	4703
rs555582398	snp	A/G	1.91258e-05	0.00309233	stop-gained, intron-variant	NEB, RIF1	GRCh38.p7	2:151516533	GCATGGGTTTTCCTC[A/G]TTCCTTTTCATACTT	4703
rs555591029	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151562455	TGGCTTAGGGTGGAT[G/T]CTTATACCAAAAAGT	4703
rs555610870	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151560205	CTGGGGATGGTATAA[C/T]AACCGGTTATCATAT	4703
rs555639331	snp	G/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151491840	AACTTGAAAACCAAG[G/T]CATGAATTTTAACAA	4703
rs555646329	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151564740	CTTGTTAGATTATTA[C/T]TCTATCAATTTAAGT	4703
rs555647608	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151491319	AATGAATAAACTTCC[C/T]TGATGCAATAGAGCT	4703
rs555651487	snp	G/T	0.00119737	0.0244387	intron-variant, utr-variant-3-prime, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151498112	TGACATTAACTGTAT[G/T]ATAGAAATGGGAAAG	4703
rs555681348	snp	A/G	0.000399281	0.0141238	missense, intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151499384	CAACGTTTTCTTTAT[A/G]CAACACCTGTATGAC	4703
rs555690038	snp	A/G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151691992	AGAAAAACCAAAAAT[A/G/T]GATCATGATTGTTAT	4703
rs555706086	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151505686	TAACAGTGTAAATAA[C/T]GCAGGCTTTATACTT	4703
rs555720977	snp	C/G	0.000399281	0.0141238	downstream-variant-500B, intron-variant	NEB, RIF1	GRCh38.p7	2:151484886	GAGGTGTACGTTGGT[C/G]ATTCGCAAGTGAGTG	4703
rs555729045	snp	C/T	0.000180489	0.009498	intron-variant	NEB	GRCh38.p7	2:151540494	GCTTAAGTGTCTTCC[C/T]AATTTCCAACCAAGC	4703
rs555736662	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151630591	CCCAGAGATGAAAGG[A/T]TGGATGAGTGGAGTG	4703
rs555737256	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151541134	TTTTGCGTGACTGCA[G/T]GAAATACAGCTTCGT	4703
rs555738592	snp	A/T	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151622647	AAATTGTACACATTA[A/T]GGCCTTCATCCTTGA	4703
rs555774189	snp	A/T	0.0182019	0.0936463	intron-variant	NEB	GRCh38.p7	2:151606091	TCCCAAAGTGCTGGG[A/T]TTACAGGGGTGAGCC	4703
rs555782688	snp	A/G	0.000497323	0.0157612	synonymous-codon	NEB	GRCh38.p7	2:151663791	GTGCACCAGCTTGGG[A/G]TCATCTTCCAGGCTC	4703
rs555785007	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151684508	ACATCCTCCAAACAA[C/T]GTTTTTGATTTATTT	4703
rs555787270	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151691294	CTGTTCCCCTGACCT[G/T]GGCCTGACTGGTCAT	4703
rs555811226	snp	A/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151614021	CTTTGAAATTAGTTA[A/T]TACAGTCACCACTAG	4703
rs555824421	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151556421	AAATAAATTTCCCAC[C/T]GTGAGTCATGGTCAA	4703
rs555871433	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151555675	AATAAAATAACAGTT[A/C]TTCCAAAACTCAGCG	4703
rs555871503	in-del	-/AAAA	0.999999	3.15785e-05	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151506610	TGGGGGAGGGATAAC[-/AAAA]GAAATCACAATGTCA	4703
rs555880328	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151606846	ATTCATTTCTGGGTT[A/C]TTTTCGTTGTTGGAT	4703
rs555968605	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151690911	GGTTCCAGGTCAAAA[C/G]AGAGTTTATTTTGTT	4703
rs555969077	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151557342	GAATCCCTGAATAGG[C/T]CAATAACAAGTTCTG	4703
rs555971855	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151577327	TCCTGATCACACAGC[C/T]TGTCTTTCAATTCGT	4703
rs556001227	in-del	-/T	0.00398564	0.0444627	intron-variant	NEB	GRCh38.p7	2:151564329	TGGCTAATTTTTGTA[-/T]TTTTTAGTAGAGATG	4703
rs556005538	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151556657	AATGAAAGAAGAAGA[A/G]CTAACTATCCTAAAT	4703
rs556005765	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151563772	TCCTAACCAGCCCCT[C/T]GATCCCCAGTAAAGA	4703
rs556029291	snp	A/G	1.65916e-05	0.00288019	missense, intron-variant	NEB	GRCh38.p7	2:151650219	GCCAGAACTATATCC[A/G]TGGCATCAGGAATGC	4703
rs556038767	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151697795	ATTGAGGCCAGGTGC[A/G]GCGGCTCACGCCTGT	4703
rs556042472	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151563172	GGCATGCACCACCAC[A/G]CCCAGCTAATTTTTG	4703
rs556063902	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151721625	TGTTTGCTATATCAT[A/C]CTTTTATTTTATCAG	4703
rs556099353	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151662536	CCCTAAACTTTTATC[C/T]TTTTTATATTTCCTT	4703
rs556100050	snp	A/G	1.65734e-05	0.00287862	intron-variant	NEB	GRCh38.p7	2:151697313	TGCCCTGAGAAAAAT[A/G]TTATTTGGAAAGTCA	4703
rs556105905	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151643609	TTTGATTGTCTAGCT[C/T]GACAATCTAGAGGCT	4703
rs556111600	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151511582	AAGCACAGCTAGGGC[A/G]CGTTAACTATGGCTT	4703
rs556175395	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151544423	CTCTATGGAGCATCT[A/G]AAAGTGTATAGATGC	4703
rs556175813	snp	C/G	3.46512e-05	0.00416226	missense, intron-variant	NEB	GRCh38.p7	2:151636294	CTTCGCAAGTCATAG[C/G]CTTTCTTCTTTGCTT	4703
rs556179522	snp	A/C	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151642443	TACCATTATTTTAAA[A/C]CATTCATCGAAACAA	4703
rs556180035	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	NEB	GRCh38.p7	2:151734851	ACTCACTCTGGTAAG[C/G]TTCACCAGGTGAGCT	4703
rs556189491	in-del	-/AAAC	5.17255e-05	0.00508528	intron-variant, utr-variant-3-prime	NEB, RIF1	GRCh38.p7	2:151497743	AGAAAGCATCCAGAA[-/AAAC]AAACAACCATGAGTA	4703
rs556196602	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	NEB	GRCh38.p7	2:151735544	GTGAGTCACCTATAT[C/T]TTGATATGGATTTGA	4703
rs556224656	snp	C/T	0.000386495	0.013896	intron-variant	NEB, RIF1	GRCh38.p7	2:151491680	CTTTTTCAGCTAACA[C/T]ACCATTAATCATGTG	4703
rs556225404	snp	A/G	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151728571	ACAACATAATGGGGT[A/G]ATTATCCTCACAACA	4703
rs556231215	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151622950	TTTAACATGAGAGAA[A/G]AGTGATTATGAAAGA	4703
rs556247275	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151576489	TAACATAAATACATA[C/T]ATATATATATATATA	4703
rs556253692	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151720610	CCATAGCATTAGAAT[C/G]GTATGAAGGTAATCC	4703
rs556307762	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151656708	GATGAATAAGCTGAG[A/T]CCCAGAGAGCTGAGC	4703
rs556314125	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151578934	TAAAAATACAAAAAT[C/T]AGCTGGGTGTGGTGC	4703
rs556323559	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151559801	CTCAGGGAGTAGGGG[A/G]CTAGGGGAGGGATAG	4703
rs556335527	snp	C/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151513232	AGGAGAGGAAGAACT[C/T]CCAAGATATTCTAAG	4703
rs556377694	snp	A/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151494429	TAGTTACAGCAAGAC[A/T]CAACCAGGATAGGCA	4703
rs556404118	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151626610	GGCGCGATCTCAGCT[C/T]ACTACGAGCTCCGCC	4703
rs556430063	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151571025	TTTCTTTTTTTTTGA[A/G]ACGGAGTTTCGCTCT	4703
rs556431017	snp	C/T	0.00199481	0.0315187	intron-variant	NEB, RIF1	GRCh38.p7	2:151518065	ACCATGAGGGGTTTG[C/T]CCCCTCATAAAACAC	4703
rs556432184	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151663008	TAATTCACCTCTCCA[A/G]CCATCAAATGGACTC	4703
rs556443343	snp	C/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151491118	TCACTGCAGCTTCAA[C/G]TTTCTAGGCTCAAGC	4703
rs556470265	snp	A/G	0.00119737	0.0244387	intron-variant	NEB, RIF1	GRCh38.p7	2:151520386	AAGTGAGATACTTCA[A/G]AATAATGAGAAAAAA	4703
rs556472871	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151663361	TAGTAGAAAACAAGA[C/T]TTTAGTTTCTAGAAT	4703
rs556473915	snp	A/C/G	3.56252e-05	0.00422035	intron-variant	NEB	GRCh38.p7	2:151725007	GACAGGCATGTACAT[A/C/G]TGAGTATATTAAGGA	4703
rs556478437	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151668916	GGGTTTAATGTGGAG[A/G]CTCAGGGTCCACACT	4703
rs556483735	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151505806	CAGGGATGGGGGCCC[C/T]TATTTAGACTGCAGC	4703
rs556486696	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151661332	TTCAAGGAGGTTGAG[C/T]TCCACAAATCATTCA	4703
rs556492694	snp	A/C/T	0.000282392	0.0118794	missense, intron-variant	NEB	GRCh38.p7	2:151619714	CGTGTACTGCTCGGG[A/C/T]GCCAATGTGGTGACC	4703
rs556542697	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151636899	AGGTTGTTTTAAAAA[A/T]TTTTAGTTAAAACAA	4703
rs556543279	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151549055	AGTTGAGTACTTGTG[A/G]AAAGTGGAGAAGGGC	4703
rs556548001	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151695953	GTCCCTGCAGGTTCT[C/G]AGAGGGGCCCCGCCC	4703
rs556557712	snp	C/G	0.00119737	0.0244387	intron-variant, utr-variant-3-prime	NEB, RIF1	GRCh38.p7	2:151497377	TTATCCACACAAACT[C/G]AAAAACTCATTATTT	4703
rs556560430	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151513804	CCAGTTGTCACAGAT[A/G]GTGTCGCTTGCTACT	4703
rs556575602	snp	A/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151719404	TTTATCAAGTAAAGC[A/T]GTTGAATAATCCCAA	4703
rs556575814	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151669320	CCAGTATTTATTGGA[A/C]AGCACTGTGGGCCAG	4703
rs556591659	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151555481	ATAACTGAAAAGTCT[C/G]CTGCTAAGAAAACAC	4703
rs556599405	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151730878	CTTTACTCTTGAGCT[A/G]TTGTTTTAATTTAAA	4703
rs556610841	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151620369	TATATATATATATAT[A/G]TATATATATATATAT	4703
rs556615183	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151719785	TTGGGAGGCTGAAGT[C/G]AGAGGATCACTTGAG	4703
rs556615209	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151711612	ATTTTAGAGTCCTGG[A/G]CCTGGGTTCAAACTC	4703
rs556619257	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151688816	TCAAAATATCTTACT[A/G]TATGTTTTCACCCTT	4703
rs556624010	snp	C/G/T	0.000116015	0.00761546	missense	NEB	GRCh38.p7	2:151554953	TTAAGCTTGCCAACT[C/G/T]GGAGGCACCGTGCTG	4703
rs556643186	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151675672	CCCTAGCAAGAATAA[C/T]AGAATTCACCAAAGC	4703
rs556660124	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151726108	TGCATAATTTATCAT[A/T]ATAAATGTTTTGGGA	4703
rs556671596	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151684581	ATTTCCCAGAGGGAA[A/T]CAGTGATAGGGTGCA	4703
rs556678490	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151631423	CAAATAGAATCAGTA[A/G]TAAAGTGCAATTCTG	4703
rs556687790	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151624880	ATGCAATGACAAGTT[C/T]AGCAAGGCTGAAGAT	4703
rs556691119	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151635444	AAGAGTGTGACCTCA[C/T]GCTTGTAAAACCAGC	4703
rs556696953	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151541049	TGATCCAAGCAAAGC[A/C]ATGTGATAAAGAATG	4703
rs556704549	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151715672	AGGAACTGAATCCGT[G/T]ATCTTAGACTCCCAG	4703
rs556708670	snp	A/C	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151660592	TTAAAATAAGAATAA[A/C]CTTTTTCTGGACTAG	4703
rs556710936	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151653785	TGGATCTTAGAGGTC[A/G]TCTGGCCCGACCTCT	4703
rs556745883	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151654305	TGGCTTTAATCTTTT[C/T]TGGCTGTGAGAATCC	4703
rs556757083	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151605036	AGAAATTAGATAATA[C/T]GATTTTAGGTCATTT	4703
rs556772125	snp	C/T	0.00597247	0.0543191	intron-variant	NEB, RIF1	GRCh38.p7	2:151492874	AGTGATTATTTTCCT[C/T]AGGTTGTGTCCAGAC	4703
rs556772291	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151647313	TGGGGTTTCACCATG[C/T]TGGCCAGGCTGGTCT	4703
rs556780530	snp	A/C	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151504987	GGGAGGGGAGAAGAG[A/C]CTTCACATGTCTACC	4703
rs556886468	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151646378	ATAAGCAGAAAATAG[A/G]TGCAATATTTCTTGA	4703
rs556896885	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151608851	GAGCTTGCAGTGAGC[C/T]GAGACTGTGCCATTG	4703
rs556930902	snp	A/C/T	0.000182571	0.0095526	missense, intron-variant	NEB	GRCh38.p7	2:151612274	TGGTCTGCAGGCTGG[A/C/T]GATACTTCCTGTCAC	4703
rs556950561	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151717043	AGTGTGACGGATAAG[A/C]TAGAACTATCCAAGG	4703
rs556985148	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151552589	AAGACTTGGCACTGC[C/T]CAGTCTATGGTTTTT	4703
rs556986127	snp	A/G	0.0023933	0.0345097	intron-variant	NEB, RIF1	GRCh38.p7	2:151494419	AAGTTAAGTGTAGTT[A/G]CAGCAAGACACAACC	4703
rs557022044	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151551915	CTTTAAAAAAAATAA[C/T]GGTAGCCTGCTTCCC	4703
rs557044334	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151619080	TAATTTAGCATAATA[C/T]GCTTTCCCTCTATCT	4703
rs557045202	snp	A/C	0.00014997	0.00865809	intron-variant	NEB, RIF1	GRCh38.p7	2:151514814	AAGACCAAGTGGGCA[A/C]TACCTCGCTTGCTAT	4703
rs557061052	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151564872	ACCAGCTGAATAAAC[A/G]CTATTTGCCTTGAAT	4703
rs557075220	snp	G/T	8.29414e-05	0.00643924	missense	NEB	GRCh38.p7	2:151679735	CGTCACTCGCCGCCT[G/T]CCTGGCAGCTTTGGC	4703
rs557106618	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151698292	AGTATACAATTCAAT[A/G]GATTTTAGTATGTTT	4703
rs557113523	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151638469	CTGGTGCTGCTCTCC[A/G]TCTCTGGGGGTTGGC	4703
rs557153254	snp	A/G	0	0	intron-variant	NEB, RIF1	GRCh38.p7	2:151492609	TTGGGTCAACTGAAG[A/G]GGCCCAGTGAGACAC	4703
rs557179412	in-del	-/T	0.00119737	0.0244387	intron-variant	NEB, RIF1	GRCh38.p7	2:151526361	CAGCGTTGACAATAC[-/T]TAAACTCAATAAAAG	4703
rs557216009	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151579013	TTGAACCTGGGAGGC[A/G]GAGGTTGCAGTGGGC	4703
rs557219100	in-del	-/TTTA/TTTATTTA/TTTATTTATTTATTTATTTA	0.614897	0.151931	intron-variant	NEB	GRCh38.p7	2:151574726	ACAGTTTAAATTTTA[lengthTooLong]TTTATTTATTTATTT	4703
rs557219422	snp	C/T	0.0023933	0.0345097	intron-variant	NEB, RIF1	GRCh38.p7	2:151494741	GCAACCTCCGCCTCC[C/T]GGGTTCAAGTGATTC	4703
rs557224425	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151703138	TAGTTTGGCTGGATA[G/T]GAAATTCTGGGTTGA	4703
rs557237512	snp	A/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151513967	AAGATTAGAGTATAA[A/T]GTAAATTGTACATCT	4703
rs557251885	snp	A/C	0.00318978	0.0398085	intron-variant	NEB	GRCh38.p7	2:151617551	TTTTGATTATGTGCC[A/C]GTCATCTCTCTTGTA	4703
rs557256600	snp	A/G	0.00279162	0.0372561	intron-variant	NEB	GRCh38.p7	2:151578518	ATAAAAAAATCAGCC[A/G]ACTGTGGTGGCATGT	4703
rs557275976	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151521645	TACTAAAAGTCCTCC[C/T]TCTGTCTTTTAGAAG	4703
rs557283502	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151672055	TTGCATTTTGTATCT[A/G]TCACCATTGCAGCCA	4703
rs557283717	snp	A/G	6.63207e-05	0.00575812	missense, intron-variant	NEB	GRCh38.p7	2:151609900	TAATTGCGATAATCA[A/G]TGTCAGTGACCAAAG	4703
rs557288737	snp	C/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151493489	TCAGACAGCAGAAAA[C/G]CAGGTCTGAAAATCA	4703
rs557299931	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151702701	AACCCCTGCCTTTTT[G/T]TTGTTTTCCATTTGC	4703
rs557311446	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151527406	ACTCATGATAGTGGT[C/T]ATTATAAATAATTAT	4703
rs557317101	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151697880	GACAAGCCTAGCCAA[C/G]AAAGTGAAACCCTCT	4703
rs557325694	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151644772	TTCAATTACCTAAAT[C/T]AGCAAAATTGTCAGC	4703
rs557356525	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151572237	TGAGGCAGGAGCATC[A/G]CTTGAACCCGGGAGG	4703
rs557363591	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151658557	AAATGATAAAAATAG[A/G]ATTAGAGGATTTCCT	4703
rs557404113	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151533371	TGGAAGAGGAAATCA[A/G]TGAAAGCATACAAGG	4703
rs557466986	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151499933	TTTTGCCTAAATGCA[A/G]TCTGTGTAAAAATTA	4703
rs557480322	snp	C/T	0.00140696	0.0264859	intron-variant	NEB	GRCh38.p7	2:151630708	CACCACAGATTTTTG[C/T]TCCTACCTCACTGTA	4703
rs557533181	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151660055	CTTTTGGCAAATAGT[C/T]TCCAGTCACCAGCTG	4703
rs557552315	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151549813	GCTTAACAAATCACA[C/T]ATAGCTCATGTTACA	4703
rs557557423	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151537388	AAAAGACATTTTCAG[A/T]AATACTGACCTTTGG	4703
rs557582375	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151678857	GGTGGGTGAGAACTT[C/T]GGGTGGGACAGGGGC	4703
rs557584808	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151564274	ATTCTCCTGTCTCAG[C/T]CTCCAGAGTAGCTGG	4703
rs557591373	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151528643	ACTAATTCGGTTACA[A/G]TGGTTTCATTGTATA	4703
rs557599229	snp	C/T	0.030665	0.119967	intron-variant	NEB	GRCh38.p7	2:151699131	GGTTTTTTGTTCTTG[C/T]GATAGTTTACTGAGA	4703
rs557611006	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151729380	ATCACACAGAAGAAA[C/T]AGGGGGAACCACCCC	4703
rs557622391	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151665046	AAAATTGTTGAATAC[A/G]GCAACCCTCTACCAC	4703
rs557634344	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151686403	TACTGCTGGGTTCTG[C/T]GATAGGAATAAAAAC	4703
rs557645705	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151622010	TGTGGGGTCTTTTTT[A/G]TTGTTGTTTTTTGTT	4703
rs557658030	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151708472	TCACTTGCTTCCCAA[A/C]GCATTGCCCTCTCCT	4703
rs557685210	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151566317	TATTCTTGCCCTTAC[A/G]CCTTCAAGAACCTAG	4703
rs557688210	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151615037	AAGGATATGTGTTAC[A/G]TTTAGATAGAGTTTA	4703
rs557688789	snp	C/T			synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151501391	CTTTCTCCCAAATAC[C/T]GAGCTAAAGTTTTCT	4703
rs557696314	snp	C/T	3.35317e-05	0.00409448	intron-variant	NEB, RIF1	GRCh38.p7	2:151492055	TTGTTCTTCTACCCC[C/T]TCACTTAAAGTTAAT	4703
rs557730486	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151652748	CTATAATAGTGGGAA[A/T]GTTCACTTATAGTTC	4703
rs557748180	snp	A/G	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151493625	AATCACTGTGACCTC[A/G]TGGGGTTGGTTTGTT	4703
rs557754227	in-del	-/TT	0.0673337	0.170684	intron-variant	NEB	GRCh38.p7	2:151664022	ACTCTTTTTACTTCA[-/TT]TTTTTTTTTCCCGAG	4703
rs557762911	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151722279	AAATCCAATGGTCAT[A/G]TAAGAAAGTACCTCA	4703
rs557809441	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151500210	AAACAAAACAGAACA[A/G]AAAGACAGTGGGACC	4703
rs557816404	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151680542	AAGGACAGTCAGCAC[A/G]ATATACATTACTGTA	4703
rs557825157	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151614152	CATACTTTATTTTGT[A/G]CATTTCAGAACATTA	4703
rs557865820	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151621283	CATTAAATGAACACC[C/T]CTTAATGTGTTTAGA	4703
rs557870969	snp	C/T	0.000399281	0.0141238	splice-donor-variant	NEB	GRCh38.p7	2:151657982	TTTCCTTTGGACTTA[C/T]ATCACTTGCAATATC	4703
rs557877968	in-del	-/A	0.474453	0.110094	intron-variant	NEB	GRCh38.p7	2:151656847	AGAACACAGAAGATG[-/A]AAAAAAAAAAGGCAA	4703
rs557879773	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151718143	CAGGCGTGAGCCACC[A/G]CGCCTGGCCAACTTC	4703
rs557882649	snp	C/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151521449	GAAGGTCTGAGGTGT[C/G]AGCTGGTGTCTGGAC	4703
rs557903450	snp	C/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151494337	GTACAGATAACTTTT[C/G]ATTATCTTTAGGGCC	4703
rs557914760	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151637103	ATGAGGTTGAGACCC[C/G]TCTCAACCTAAAGGT	4703
rs557950249	snp	C/G/T	0.000132666	0.00814341	missense, intron-variant	NEB	GRCh38.p7	2:151643843	AGGTCATAGGCCTGC[C/G/T]GAGCATGGATGACAT	4703
rs557951728	snp	G/T	9.08389e-05	0.00673878	missense, intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151498281	AAGGTTTTCTTGATT[G/T]TGTTTGACTCTCTGC	4703
rs557976927	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151541244	CTTAGGAAAGAAGAT[A/G]TGGCATCCCTTACCT	4703
rs558001311	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151523683	TCATGTGGTAACTGG[A/G]TTTGGGCAACACATT	4703
rs558010091	snp	G/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151501003	CCTGTTCCTAAGGAA[G/T]AGCCACCATTTCTAT	4703
rs558019875	snp	A/G	1.6784e-05	0.00289685	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151485773	GCCTAAATAGCTTCA[A/G]CGTAGTTGGCTGGGA	4703
rs558020281	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151632413	AGGTGTTGGGGTCCA[C/T]GCCTGTAATTCCAGC	4703
rs558022715	snp	A/G	1.65614e-05	0.00287757	synonymous-codon	NEB	GRCh38.p7	2:151672510	TGTGATGCTAACCAT[A/G]TCCCCAGGGGTATGG	4703
rs558033751	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151492551	TCTGAAACCTCAAAG[C/T]CTTTCCAGCAGATAG	4703
rs558034027	snp	A/G	0.000399281	0.0141238	downstream-variant-500B, intron-variant	NEB, RIF1	GRCh38.p7	2:151485076	CTTTGCCTTTGCCAC[A/G]TGCTGCCATCCTACT	4703
rs558035288	snp	A/G	0.000199621	0.00998852	intron-variant	NEB	GRCh38.p7	2:151716101	AATTGTCCTTCTCCC[A/G]TCTTATTTACAATAT	4703
rs558091865	snp	G/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151527358	CCAACCATCCTCCTC[G/T]CCTTCTCGGATCTCA	4703
rs558092001	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151606337	CATTGTATTGGGTCC[A/T]GAATTTTCCCAGGAA	4703
rs558098358	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151657147	TTGGGGGTAGAAGCT[A/T]GTAGAGCCAAATTAC	4703
rs558115292	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151616355	AATCAACATTTGGTT[A/G]GCAAAATTTTATTTG	4703
rs558120873	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151706420	TTTAAATTGAACGGC[G/T]TAGTCGGGCTCTTAA	4703
rs558150698	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151577920	TTCACCATGGTATCT[C/T]TAGTGCTTAGCACAA	4703
rs558152102	snp	C/T	7.7009e-05	0.00620472	intron-variant	NEB	GRCh38.p7	2:151664469	TTGTTCTTACTTGCT[C/T]AACCCCAAAAAGGCC	4703
rs558178555	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151541882	TCCTGTTTTCCCAAT[C/G]CCCTCTTTTCACCTG	4703
rs558185112	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151709905	TTACAATTAGAGAAT[A/G]TGGTACCATTACAAA	4703
rs558185248	snp	C/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151718409	CTAATGCCATTTTGT[C/G]TTCAAGGAAACTTTC	4703
rs558189577	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151606908	TTAAAATTTTAAAGC[C/T]AAACATCAAACTCTA	4703
rs558228679	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151583907	ATTACATATTTCAGT[C/T]CACTTTAAAGAAGTT	4703
rs558230126	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151610927	AAGACCTTCTGTTAA[A/G]GCCAATAACATCATT	4703
rs558242409	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151605504	CAGAAGATAACAACA[A/C]AAGTTCTGTGGACAA	4703
rs558259277	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151704462	CCCTCCCCCAGCCTC[A/G]CTGCCGCCTTGCAGT	4703
rs558265511	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151573847	CTGGATTATCTTGTA[C/T]TCACAAATAGTTTTT	4703
rs558275246	in-del	-/CCTC	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151626221	CCAGGCTCAGGTGAT[-/CCTC]CCACCTCAGCCTCCC	4703
rs558294677	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	NEB	GRCh38.p7	2:151735810	TTATACCTGTTCATC[C/T]TGTATGTTCTCACAG	4703
rs558313733	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151641537	TGCCTTGCTATGTTG[A/G]CCAGGCTGGTCTCAA	4703
rs558345996	snp	C/T	9.94975e-05	0.00705258	missense	NEB	GRCh38.p7	2:151568407	GCATTCCAGTCTTTC[C/T]GGTATTTAATCTAAA	4703
rs558350064	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151570058	CTGAGAAAAGAGTTC[A/G]ACCCCAAATGCAGCC	4703
rs558430454	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151671294	GGATGTTTCTGGGAT[A/C]TGCAATTCTATCCAA	4703
rs558432537	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151732816	TCCCTTTGAACATCG[C/G]GGTTGGGAAGTGGGG	4703
rs558437971	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151513446	CATTGGGATGGCTTC[C/T]TCCAGGCAGATGTTC	4703
rs558439149	snp	A/G	6.62669e-05	0.00575578	missense	NEB	GRCh38.p7	2:151692078	CTGTTTTGAGCTGCA[A/G]CTTTCATGCAGTGTG	4703
rs558447104	snp	A/C/T	0.000184132	0.00959368	intron-variant	NEB	GRCh38.p7	2:151592012	GAGCACTGTGAAAAG[A/C/T]AAATGATGTGCGCTG	4703
rs558451254	in-del	-/TTTG	0.0020036	0.0315878	intron-variant	NEB, RIF1	GRCh38.p7	2:151486888	CAATGGGCACCAGCA[-/TTTG]TTTGTTTGTTTTAAT	4703
rs558453081	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151533269	CGGATGACCACTGTC[C/T]CATCACCTTTGGCCA	4703
rs558453820	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151648550	GCAACACACATTGTA[C/T]CCACCAAGCAAACAG	4703
rs558457083	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151525866	AAGAGTGAAGCTACA[C/T]AAAGGAAGCAAAAGG	4703
rs558463697	in-del	-/T			intron-variant	NEB	GRCh38.p7	2:151632164	CACTTTATTAAAAAA[-/T]TTTTTTTTGCTGAAG	4703
rs558500998	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151529099	GGCCTGACTCTTGCT[C/T]TGGAATCAATCACTA	4703
rs558563333	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151502117	AGTGAAGTAACTCAG[A/G]AATGGAAAACCAAAC	4703
rs558576817	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151687314	CTTTTGTGAATGTGA[G/T]GTGAAAGAGCCCATG	4703
rs558577048	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151546294	GAGGCTGGTGATGGG[A/G]GCATCCAGCTGTGCG	4703
rs558580429	snp	A/G	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151489597	AGATGAAGTCTCACT[A/G]TGTTGCCTAGGCTGG	4703
rs558583733	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151538060	GAGAATTTCAGAAGA[C/G]GGAGGTTGCTAAAAA	4703
rs558588239	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151535913	AACTAACACATATTC[A/G]TTTGTTTGTTTTGAG	4703
rs558594730	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151534852	TAATTCTTCAGGGTT[G/T]TCCAGTCTGGAAATC	4703
rs558601807	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151537365	ATAAAGTATTAAAAC[A/C]ATTATTTAAAAGACA	4703
rs558657964	snp	C/T	8.60237e-05	0.00655778	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151502793	CCCCCTAAGAAATAC[C/T]GAGCTAAAGTTCTCT	4703
rs558663009	snp	A/G	0.00159617	0.0282053	intron-variant	NEB, RIF1	GRCh38.p7	2:151503294	TAAAAAAGATGGGTT[A/G]TTGTGGTAAATTTTT	4703
rs558682746	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151731165	AAGCAGCTCCTTGGA[A/G]ACCATTCAATTTTAC	4703
rs558704229	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151517292	GAAGACCCTCATGCA[C/T]GCAGCACCTTGATGG	4703
rs558704335	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151550754	GGTAATCTTTTCACC[C/T]CAACCTCCCAAGTAG	4703
rs558719999	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151660754	AACAGCTGTGGTTGT[A/G]TCACTATAAAACTTT	4703
rs558763531	snp	G/T	2.06281e-05	0.00321149	intron-variant	NEB	GRCh38.p7	2:151568061	ATGCACTCCCATCAG[G/T]ATGTATTACCTCACT	4703
rs558766064	snp	A/G	0.00279162	0.0372561	intron-variant	NEB	GRCh38.p7	2:151572895	AAAAAAAAAGCCCGG[A/G]GCCTGAGACCCAATG	4703
rs558788206	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151694720	TAAATACCTTATCTT[A/C]ATATAAAATAAATGG	4703
rs558788763	snp	A/G	0.00318978	0.0398085	intron-variant	NEB, RIF1	GRCh38.p7	2:151494705	CCAGGCTGGAGTGCA[A/G]TGGCACGATCCCTGC	4703
rs558798089	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151575290	AATTTTGGTCACTTA[C/T]GATTTTCTAGAAAAC	4703
rs558804962	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151579186	ACAATGAAAACTTTC[C/T]GAAGAAACCTGGCTG	4703
rs558809946	snp	A/C	2.51386e-05	0.00354523	intron-variant	NEB, RIF1	GRCh38.p7	2:151531118	TGAAAGATCAAAAAG[A/C]AGAAAGACATCATGT	4703
rs558829102	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151566532	CTCTGGGCACCTAAG[A/C]AACTAAGTTGATGCA	4703
rs558837275	snp	A/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151502217	ACTTTGGGGACTTGC[A/T]GGAAAGAGTGGAAGT	4703
rs558838602	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151682403	ATGGCTAACATAAAT[A/G]AATGGTTAACGTAAA	4703
rs558850676	snp	A/G	0.00119737	0.0244387	intron-variant	NEB, RIF1	GRCh38.p7	2:151530667	CCCAGGCATGTGGAG[A/G]GGCCACATGAAGGGG	4703
rs558890527	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151646321	ATTGCTGAATTTATC[G/T]GAATTAAACATTATA	4703
rs558895238	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151487331	TCCTAGGAGCAGCCA[C/T]TGGTTAGTAGTTTTG	4703
rs558896753	snp	C/T	2.3011e-05	0.0033919	intron-variant	NEB, RIF1	GRCh38.p7	2:151516414	AGAGCTTGTGTTCAG[C/T]AGTGTGATGGATCAT	4703
rs558897486	in-del	-/AGCTGACCACTGCTCCTACATACACACA	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151664414	ACCAACCCTGAATGG[-/AGCTGACCACTGCTCCTACATACACACA]AGCTTAGCGCATTTG	4703
rs558935171	snp	C/G/T	3.31429e-05	0.0040707	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151529266	GAACAGCATCTGGCT[C/G/T]AATGGTGCAGTTGGA	4703
rs558974602	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151702677	TGTTTTATCAGAGAC[G/T]AGGATTGCAACCCCT	4703
rs558976070	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151639430	AAAAAAGTTCTGTGT[A/C]TAGTTAATAGGAATT	4703
rs558978223	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151559365	AAACTAGTTCAACCA[C/T]TGTGGAAGACAGTGT	4703
rs558980498	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151651691	ACTAGATGACAATAA[A/C]AACAGTGATAATAAT	4703
rs558993290	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151581442	AAAGGTTTGGTTAGG[A/C]AGAGAGCACTGTGAA	4703
rs558995519	in-del	-/T	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151680463	GAAAAAGGCTTGTAG[-/T]TTTTGTTGTCATTAA	4703
rs559010148	snp	A/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151673453	AAAAAAAAAAAAGAA[A/T]AAAAAAGAATAAAGT	4703
rs559020888	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151535386	GAGTTCCGCTGACAG[C/T]CAAGAAAATCCTTTA	4703
rs559034846	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151523952	TCATTGCTCTTCATG[C/T]TAAATCTATCCCAGG	4703
rs559049450	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151653734	TTGCAATCTCGGGTC[C/T]TTTGTAACATCTCCA	4703
rs559062262	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151617105	ACAGTGACCTGTAGG[A/G]GAAGGTTTTAAAAGT	4703
rs559067790	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151673953	GTGAGCCACCATGCC[C/T]GGCCAAAATTTTGTT	4703
rs559070193	in-del	-/TTTG	0.0715223	0.175059	intron-variant	NEB	GRCh38.p7	2:151595421	ACGCCCAGCTAAGTT[-/TTTG]TTTGTTTGTTTGTTT	4703
rs559105961	snp	G/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151722005	GTGATATGAAGAGGG[G/T]GGCGTTAAAAATTAG	4703
rs559136603	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151645619	TAATACATTCTTTAA[C/T]GTTAAAGTCATTCTA	4703
rs559144143	snp	G/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151523699	TTTGGGCAACACATT[G/T]CTGAGTCCATTTGCT	4703
rs559180928	snp	C/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151522911	CCCTTGGGCCCAGGG[C/G]CACACCATGAAGCTG	4703
rs559182058	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151494690	GTCTTGCTCTGTCAC[C/T]CAGGCTGGAGTGCAA	4703
rs559204422	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151632963	AGCTACAGAACAGAC[A/G]TGGGAGTTTTCTCAG	4703
rs559215916	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151609142	TTTTAAGGGATGGAG[C/T]GCAATTGGAGATTGC	4703
rs559226181	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151681265	CAAGAAGCTGTCCGG[C/T]TGAGGAAGGAGGAAT	4703
rs559228102	snp	A/C	0.00279162	0.0372561	intron-variant	NEB, RIF1	GRCh38.p7	2:151501144	TCAATTAACTTCAAC[A/C]GTCCCAACAACATAA	4703
rs559266998	snp	C/G			intron-variant, utr-variant-3-prime, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151497872	TGGAAGCTGTTGTTG[C/G]GATAGGGAATCTGCA	4703
rs559268680	snp	C/T	9.65298e-05	0.00694662	missense, intron-variant	NEB	GRCh38.p7	2:151579352	CGTCGCTCTGTAGGT[C/T]GTAGGCTTTCCTGGC	4703
rs559287425	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151732077	TTTCCAAAGAGAAAT[A/T]TTGGCACTGCCACCT	4703
rs559289928	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151729109	ATATTTATGGTAATA[C/G]GTTATTTAGAATTGC	4703
rs559295305	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151529030	TCTTCCCTATGCTCC[C/T]TTGTGAGGACCAATG	4703
rs559305221	snp	G/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151609621	TATATTTGTCTGAAA[G/T]ATGTTTTCATTGCCA	4703
rs559330245	in-del	-/TC	0.0158469	0.0875917	intron-variant	NEB	GRCh38.p7	2:151706337	TCATCACATATTCAA[-/TC]TCTCTCTCTCTCTCT	4703
rs559331503	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151535224	GGAGTAACAATGGCA[A/G]TATCTTTGAAGCATG	4703
rs559340875	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151515863	AAACAATTTTTCTTT[A/G]TAGTTGGAGGAAGAG	4703
rs559349183	snp	A/G	0.00358779	0.0422022	intron-variant	NEB	GRCh38.p7	2:151687001	TAGACCAAACTCATT[A/G]CTAAAGTCAATGAAG	4703
rs559387525	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151665971	AATCCTAAAACTCTG[A/G]GTTCTGGAGGGAATC	4703
rs559391024	snp	C/T	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151702361	GTTTGGGGTGGAGAG[C/T]TCTGTAGATGTCAAT	4703
rs559415895	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151693096	AGCACTTGGTGAAAA[C/T]GCATTTTGTAACACC	4703
rs559417107	snp	C/G	0.000356506	0.0133464	missense, intron-variant	NEB	GRCh38.p7	2:151581543	AGTGTCAGCTGGCAC[C/G]TTCACATTAGCCTTC	4703
rs559424609	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151659737	ATTTTCTGTGTAAAT[G/T]AAAACAGACATATAG	4703
rs559445859	snp	A/C	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151564241	CTCACTGCAAACTCT[A/C]CCTCCTGGGTTCAAG	4703
rs559449354	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151578063	TGCATTTTAAGTGAT[A/G]AGCATGCTTTCCTGT	4703
rs559449907	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151642211	TTCAGCCCTTGTAGA[G/T]TCATTGGTTCATACA	4703
rs559501599	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151552004	GCGTGTGGACACTCA[C/T]ACTGAGAAACAGAAG	4703
rs559513122	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151571155	GGATTACAGGCATGC[A/G]CCACCAGGCCCAGCT	4703
rs559519959	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151556110	TTTTGTAATCTTCCA[A/G]ATAGAGGTGGGTCTG	4703
rs559522444	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151639560	ATGTGTATTTATAAA[C/T]GCCTTCTAATAATCT	4703
rs559531040	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151623844	TATAAGTGGGAAAAA[A/G]TGTGCTTCAATCATC	4703
rs559543039	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151500670	GGCACAATCACGGCT[C/T]ACTGCAGCCTTGACT	4703
rs559556429	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151731397	ATTTCAGATGTCCAA[C/G]ATCCCAAGGAGATAT	4703
rs559632362	in-del	-/ATA	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151662701	ATGCTGACCTTTCTT[-/ATA]AAAATTCCCAAGTCC	4703
rs559660789	snp	C/T	0.00358779	0.0422022	intron-variant	NEB	GRCh38.p7	2:151722392	TTTAAGTTCCTCTAA[C/T]ATACAGTTTTCAAGG	4703
rs559669058	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151715692	TAGACTCCCAGCCTC[C/G]AGAACTGTGAGAAAA	4703
rs559674933	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151568913	TTATGCCTCCCACAG[A/T]TTTTAAAGTAGGAAG	4703
rs559680312	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151566144	TTTTCTGCTATCGTC[A/G]TAAGAAAAGGCTTAC	4703
rs559687247	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151725733	AAATAGATTTGATAA[C/T]TGCTTCTCCTAAACA	4703
rs559711349	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151708002	AACTTTACTCTCCCC[C/G]TACCCGCATCTGGGA	4703
rs559720970	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151646711	CTGGAGTGCAATGGC[A/G]CAATCATGGCTCACT	4703
rs559737682	in-del	-/TT	0.00199481	0.0315187	intron-variant	NEB, RIF1	GRCh38.p7	2:151532840	TGCATCAAATTTACC[-/TT]TCAGCATGTGCTGGA	4703
rs559800794	snp	A/G	0.000798403	0.0199641	missense	NEB	GRCh38.p7	2:151692283	AAGTTCTTCAGCTGA[A/G]TATCAAGTTGATATT	4703
rs559804968	snp	A/T	0.000399281	0.0141238	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151485932	ATGGCACGGAAGATT[A/T]TCTATTCGTGGGGAT	4703
rs559816364	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151557857	TAAACTAGGTATTGA[C/T]GGAATGTATCTCAAA	4703
rs559823585	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151678284	TGAGCTTCCCAAAAA[C/T]TACTGTACTTCAATA	4703
rs559846137	snp	A/G	9.93608e-05	0.00704773	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151644016	CTTCTTGTACTCCCT[A/G]TCACTCTGGATCTTG	4703
rs559862729	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime	NEB	GRCh38.p7	2:151733729	CAAGGCAATGGGGTT[A/G]TTTTCTTCCCGAACA	4703
rs559888560	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151620680	CATCTAGCTTTAATC[C/G]AGGCACTCACTCCTA	4703
rs559890495	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151719964	TTCATGGCTGGTTAA[G/T]TCCTTAGGGTAAAAG	4703
rs559914745	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151533255	TGTCAGATGATGTAC[A/G]GATGACCACTGTCCC	4703
rs559942697	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151681358	TAATGTGGTTAGTAC[A/G]TAAGTTATCACCAAA	4703
rs559977860	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151717021	GAGACACATTCTTAT[G/T]TTTCCAAGTGTGACG	4703
rs559979682	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151558691	TCTGACAAAAACAAG[C/T]GATGGGGAGAAGACT	4703
rs560007979	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151676860	CTATATCCCATGAAT[C/T]CTCATCTATTTCATC	4703
rs560043429	snp	A/C	0.00022542	0.0106141	intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151497063	AGCAACCAGAAAAAC[A/C]ACCATGAGTAACATT	4703
rs560054416	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151719595	CTTAATTTCTTTTAA[A/G]TAAGTTAAGCAAGGC	4703
rs560064368	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151678919	ATCACATATTTACAC[A/T]GGTGCGATGTAAACC	4703
rs560070870	snp	C/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151667652	CCCATCTCAGCCTCT[C/G]AAATAGTTGGAACTA	4703
rs560075959	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151627428	GAGAAGAAATGTCAT[A/C]CCTTCTGAAGGTTCT	4703
rs560104581	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151712670	ATGGCCTTCTGTCTC[A/G]TTTGTGAGTAGGAGA	4703
rs560109089	snp	A/G	4.97228e-05	0.00498587	missense	NEB	GRCh38.p7	2:151548366	ACATCTTTGGGGCCA[A/G]GTGTATACCCATATG	4703
rs560114260	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151634492	ACTAAAAATAAAAAA[A/G]TAAGCCGGGCGTGGT	4703
rs560132337	snp	A/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151514151	ATTCATCAGAAATTG[A/T]GGTATATTTTATGTA	4703
rs560136842	snp	A/T	0.0263992	0.111815	intron-variant	NEB	GRCh38.p7	2:151561597	TTTTTGGTTTCGAAC[A/T]CTTTTTTTTTTTTAT	4703
rs560160030	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151545642	CCCCTCATCAGCCCT[A/G]GACATAGGAAGAGCC	4703
rs560175225	snp	C/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151510517	TGAGGTTTCACTTTC[C/G]ACGGTTTCAGTTAAC	4703
rs560191386	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151673568	TTTTCAGTATCATTC[C/T]TACAAGGAAAGTAGC	4703
rs560204569	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151682535	TGGGTAATTTGTGCA[C/T]GTGGTAAGCTCTTTT	4703
rs560213816	snp	A/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151517614	CTTACACAAACCTAG[A/T]TGGTATAGCCTACTA	4703
rs560218553	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151732968	AATTATAGTGAAACT[A/G]AACATAAAATATTCC	4703
rs560227110	snp	A/T	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151674273	AAAGCCACTGTCAGA[A/T]TTATGACAGCTCTAC	4703
rs560231650	snp	C/T	0.000198708	0.00996568	missense, intron-variant	NEB	GRCh38.p7	2:151640555	TCTTGTACTCCCTGT[C/T]ACTCTGGATCTTGGC	4703
rs560249045	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151663172	CCGGTTGGGAGGGAG[A/G]GGCTGGAGCTATCAG	4703
rs560249971	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151641112	AGATTCAATAAAAAT[C/T]ATCTTTGCCTGCAAA	4703
rs560271695	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151711984	ACAGAAGTCAATAAA[A/G]TTGATTTCTGGATTT	4703
rs560294490	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151569764	TGTCTGTGCCTACAT[C/T]CTGTCCATGGGCTGC	4703
rs560300260	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151617535	TTCACAGATATTATT[G/T]TTTTGATTATGTGCC	4703
rs560312070	snp	C/T	8.28027e-05	0.00643386	synonymous-codon	NEB	GRCh38.p7	2:151694401	GACTCCAATCATTTT[C/T]CCTTTGTTTTTTTCA	4703
rs560319608	in-del	-/AC	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151671942	TTTAGATGACTCATT[-/AC]AGAGATTTACATGGA	4703
rs560347906	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151696394	GGTTTTGTTTGACTC[C/T]AGAACTCATGTTCTT	4703
rs560365791	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151704550	GAGCCAGGTGCAGGA[G/T]ATAATCTCGTGGTGC	4703
rs560366733	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151560751	AATGCATCTGGTTAG[C/T]TTCTGAGTAGCAGGT	4703
rs560410986	snp	C/G	0.00318978	0.0398085	intron-variant	NEB	GRCh38.p7	2:151693458	GTGTGTGTTGCACCC[C/G]CCATGTATCCATGTG	4703
rs560418316	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151515071	TCACACATTTGAAAC[A/G]TGTATGATTGTACTT	4703
rs560424395	snp	A/G	0.00119737	0.0244387	intron-variant	NEB, RIF1	GRCh38.p7	2:151503846	ATACTCTATTCCTTC[A/G]GGCTTATTGAGAATT	4703
rs560431879	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151633499	ATGAAGTCTATTAGT[A/G]TATTCATAATAAAGC	4703
rs560433734	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151547920	TAGGTGAAGAATTCT[A/G]AGCACAAAGCCTTCC	4703
rs560440121	snp	C/T	0.000552639	0.0166137	intron-variant	NEB	GRCh38.p7	2:151592156	GGGAAAAATGAAAAA[C/T]GATGGAATGGTCAAT	4703
rs560447668	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151542434	CTGAATTTAGGTGAT[A/T]TACCATGTTCAATAT	4703
rs560477170	snp	C/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151511166	TAAAAGGCTGGTGAG[C/G]CTCTCACAGCCCAAA	4703
rs560479496	snp	G/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151494987	CTGTTTTGCAGCACT[G/T]AAACTCTCATAGACA	4703
rs560490281	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151545049	TCATCAAGGAACCAA[C/T]ACTCTAGGTGAGAGA	4703
rs560492956	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151626623	CTCACTACGAGCTCC[A/G]CCTCTCAGGTTCACA	4703
rs560508569	snp	A/G	0.00636936	0.0560724	intron-variant	NEB	GRCh38.p7	2:151704705	GTGAGGCAATGCCTC[A/G]CCCTGCTTCGGCTCA	4703
rs560519235	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151732338	CGGTGAGGAAAAACC[A/G]TAAGATGATAAAAAC	4703
rs560550775	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151502326	CACCACTAAAGAACT[C/T]AGTAACCAAATACCA	4703
rs560561105	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151662505	CCAATAGCATGTTGA[A/G]CTTCAACCATTTCTT	4703
rs560608623	snp	C/T	1.854e-05	0.00304461	intron-variant	NEB	GRCh38.p7	2:151724820	GAGGTGATGCACATG[C/T]TACTGAGTACCCCAG	4703
rs560618706	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151552879	CTCATGAGATTTATA[G/T]TCATCAGCACTACTC	4703
rs560619586	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151611730	TGGATTTCCATAACC[C/T]AATGTGGAGGAGCAA	4703
rs560630772	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151628443	AAAATGGAATATGTA[C/T]CTACAAAAAAGCATT	4703
rs560634136	snp	G/T	0.0023933	0.0345097	intron-variant	NEB, RIF1	GRCh38.p7	2:151489758	TGCTCTAGGTTTGGG[G/T]TTTTTTTTTAAGTTA	4703
rs560635876	snp	C/T	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151647405	GTGAGCCATCGTGCC[C/T]GGCTAAAACTAGGAA	4703
rs560651819	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151662044	AAGTGTGATGCCCTA[C/T]AACTGTATTAGCAAA	4703
rs560665343	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151509182	AGCAGTTTCAGCCAA[C/T]GAGAGATGTAGGCCT	4703
rs560707978	snp	C/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151503730	TGAGAAAAATCTAAC[C/T]ATTTTGTTGCATCTA	4703
rs560724451	snp	C/T	0.00318978	0.0398085	intron-variant	NEB	GRCh38.p7	2:151627912	TTTAAAACTTTATTA[C/T]TTTAAAATTGCTAAT	4703
rs560737063	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151524753	CTCACTGCAACTTCT[A/G]TCTCCCGGATTCAAG	4703
rs560751992	in-del	-/AATTGCA	0.0170251	0.090679	intron-variant	NEB	GRCh38.p7	2:151632916	TTTCTTTTTGGAAAG[-/AATTGCA]AATTGCAAAACACAG	4703
rs560763551	snp	C/T	0.00358779	0.0422022	intron-variant	NEB	GRCh38.p7	2:151688654	GCACTGAACCCTATA[C/T]ATACCATGTTCTTTC	4703
rs560773553	snp	G/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151530189	TACAGCAATCATTCT[G/T]CCTTTTAAAAATATA	4703
rs560800486	in-del	-/TTG	0.00318978	0.0398085	intron-variant	NEB	GRCh38.p7	2:151709471	AATTCCAAAGTACTT[-/TTG]TTGTTGTTCTTGTTG	4703
rs560831825	snp	G/T	0.0023933	0.0345097	intron-variant	NEB, RIF1	GRCh38.p7	2:151488951	TTTAATAGCTTTATA[G/T]TATGTTTTGTTCTTT	4703
rs560832815	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151661069	CCCTGCTGTTGACCC[A/G]CTGTGTGGGAGGTGC	4703
rs560836580	snp	A/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151591269	ATTCCATTTAAATAT[A/T]ATTCAAAGGGCATTA	4703
rs560873675	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151611102	GAAGCAATATAATGG[C/T]TGCTATTAGTAATTC	4703
rs560893884	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151567602	TGTTTGACACCCCCA[A/G]CTCTGAGAGCAAATA	4703
rs560896756	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151725627	GCAACATACTCACCC[C/G]ATTTGATAAAAAAAA	4703
rs560918131	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151530033	CAGTTATAGCTATTA[C/T]CATATCGTGTTATAA	4703
rs560929947	snp	A/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151510378	TGTTACATCCCAGCC[A/T]TTGTACAGGGACACT	4703
rs560937315	snp	A/C			intron-variant	NEB, RIF1	GRCh38.p7	2:151524084	TTAAGCACACAGACA[A/C]CCAGACAAATGCCCA	4703
rs560950509	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151644202	TGGCAAATTACAAAG[C/T]GCATTAACTCTAAAT	4703
rs560964775	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151654477	AGAAAAACAGGTCAC[A/T]ACATTTTAATTAGCT	4703
rs560965487	snp	A/G	8.27945e-05	0.00643354	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151640451	CTTGTAGTCCACATC[A/G]CTGACTAAGGTCTGG	4703
rs561010990	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151697090	ACATTTTAAACATAT[C/G]CTGACCACTAGATGC	4703
rs561020159	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151675447	CTATTAATTGTTTGC[C/T]TTAAAGAGTTATTTT	4703
rs561026006	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151687351	AAATTCTTTTCCACA[C/T]TACTACCCTTGGGCA	4703
rs561026516	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151631567	TTATTAGGAGAGGAG[C/T]GATCCCAAGTAATAT	4703
rs561028222	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151665256	AAACACTGTAGGAGA[C/T]GATTGGGGCACTGCC	4703
rs561031675	snp	A/G	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151559492	AAGACACATGCACAC[A/G]TATGTTTATTGCAGC	4703
rs561041344	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151688220	ACAATTCCTTGTCTT[G/T]TCTTTTAAAATTTAA	4703
rs561060029	in-del	-/TTTTC	0.00636936	0.0560724	intron-variant	NEB, RIF1	GRCh38.p7	2:151501112	GCTTTAGTGTTTGGT[-/TTTTC]TTTTCTTTTCTGGAA	4703
rs561076178	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151647352	TGATCGCAGGTGATC[C/T]ACCTGCCTCGGCCTC	4703
rs561088562	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151663163	GAATGAAACCCGGTT[A/G]GGAGGGAGGGGCTGG	4703
rs561088574	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151711024	TAGAGTTAAATTTAA[C/T]AGGAACTGGAAAGTA	4703
rs561088816	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151675663	ACCATGAAACCCTAG[C/G]AAGAATAATAGAATT	4703
rs561112290	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151716788	AAGTATTTAAAAGCA[G/T]CAGTATCCCAGGAGA	4703
rs561116004	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151554394	AACGAGATTCCAATC[A/G]CTACAAAAAAAAACC	4703
rs561121659	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151517857	CTGTCATACAGGTGG[C/T]CTGCTGTTGACCAAA	4703
rs561123550	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151718809	CCCACAAATAATGCA[C/T]ATCCTTCTCTCTTGC	4703
rs561141464	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151709976	AGGCTAAAAACAGAA[G/T]TAGAAAGGCTTTTCT	4703
rs561143244	snp	C/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151702924	TATGATGTTAGCTTG[C/G]TCGTTAGTTGATGCA	4703
rs561160404	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151704566	ATAATCTCGTGGTGC[A/G]CCGTTTTTTAAGCCG	4703
rs561161116	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151581239	TAGGTATTACTCTAC[A/G]TGTATCTATAAGTTT	4703
rs561180172	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151704513	TAGCAATCAGCGAGA[C/T]TCCGTGGGCGTAGGA	4703
rs561183277	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151519984	GATCACTGGCCTTGC[C/T]CATTTTTATATTATT	4703
rs561190918	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151547786	AGTAGGGGACGACGA[C/G]GGCATCTACTGACTA	4703
rs561204709	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151709315	ACAGCAAAAGGCCCT[G/T]CCAGTGAGAAGACAC	4703
rs561259760	snp	A/C	2.17867e-05	0.00330044	intron-variant	NEB	GRCh38.p7	2:151560987	CATATATAAGGGGGA[A/C]AAAAAACTCAACTCA	4703
rs561268084	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151509688	GCTAGAGTCCAGTGA[C/T]GTGATCTTGGCTCAC	4703
rs561277838	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151707653	GGCAGGGTTCACAAG[A/C]CCCCATCAGGAGCCT	4703
rs561297238	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151670701	AATAAATAGCTTGTT[C/T]TGCAATTCATACAGA	4703
rs561322654	snp	A/C	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151724097	GCTTTCCTCTCAGTT[A/C]CTTTTTGCCAAGCCC	4703
rs561355105	snp	A/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151508474	TGGGCTGGATGAAGC[A/T]ATGTAGCCAGACTGT	4703
rs561358756	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151717291	GAGTCTTTGGGGATC[A/G]TATGTAAAAATACTC	4703
rs561380484	snp	C/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151717903	ATGTTGCCCAGGCTG[C/G]AATGCAGTAGCGCGA	4703
rs561382896	in-del	-/T	0.00993419	0.0697739	intron-variant	NEB	GRCh38.p7	2:151667176	TTCTATTTCCATGGA[-/T]TTTTTTTTCTTCATG	4703
rs561396121	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151548795	TGATTTTAACCAACC[A/G]TTTTAACACATCCTT	4703
rs561402352	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151539470	CTCGGGCTTACTGCA[A/G]TTACCTTAAGATGCC	4703
rs561427003	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151676321	AGCTCCTTCTCTGCC[A/G]TTGCTACTGCCTTAG	4703
rs561429482	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151653931	ATAAAAATAGTTACC[A/G]ACATTAAGTCACCTG	4703
rs561432979	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151556025	GTTCATGACTCAAGG[A/G]AAAAGCCTCTTTTGA	4703
rs561445832	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151667629	AACTCCTGGGTTAAA[A/G]AGATCCTCCCATCTC	4703
rs561450014	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151551909	GTTCCTCTTTAAAAA[A/T]AATAACGGTAGCCTG	4703
rs561457300	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151566031	ATGAATAAGTATAAA[A/G]AAGGAGTCTAGGAGT	4703
rs561461904	snp	A/C			intron-variant	NEB, RIF1	GRCh38.p7	2:151511060	GCCAAAGAGAGCCCC[A/C]GGAGAGCAGAGCAAG	4703
rs561474254	snp	A/C	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151515051	AATCATAGTTCTGCT[A/C]ATGGTCACACATTTG	4703
rs561494024	in-del	-/G	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151687016	ACTAAAGTCAATGAA[-/G]AACGATACTCTATTA	4703
rs561512571	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151721103	ATCCAATGCCATTCA[C/T]GCCTATTAATACTTA	4703
rs561514158	snp	A/G	0.00438332	0.0466095	intron-variant	NEB	GRCh38.p7	2:151577648	TGCAGTGGCAATCTC[A/G]GCTCACTGCAACCTC	4703
rs561542607	snp	A/G	3.0801e-05	0.00392422	synonymous-codon	NEB	GRCh38.p7	2:151706910	CTCCTGCTGCCTTCA[A/G]CTGCCTAAGCTGTGG	4703
rs561551965	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151494891	CTGACCTTGTGATCC[A/G]CCCACCTTGGCCTCC	4703
rs561553901	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151713668	GGACTTTCCAGTGTC[A/G]CATTCAGGGCCCCAC	4703
rs561582746	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151542215	CTGTCTTTTAGACCT[C/T]CTCATCAGCCTTCCT	4703
rs561592841	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151545445	CCAGGCGTGGTGGCA[C/T]ATGCCTGTAATCCCA	4703
rs561611191	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151706533	CCAAGATCTATCTTT[C/G]AAAGTCTCCTTCTGC	4703
rs561613991	snp	C/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151502261	AAAACACTACAAATA[C/T]GGTGCAGTGTATACT	4703
rs561626081	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151497892	GGGAATCTGCACCCT[C/T]TAGAGAAGCAGGGAC	4703
rs561644740	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151621686	AGACAAAACACAAAT[G/T]TTCCATGGAAGTGTC	4703
rs561682763	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151620752	CCAGTCTAGGCTATG[C/G]CTCTGTGATGCTTGT	4703
rs561682789	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151629452	GCCAATAAATGTGCT[C/T]AAACTGGCCCCCAAA	4703
rs561703073	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	NEB, RIF1	GRCh38.p7	2:151485500	TTCAAAATCCCTGTT[C/T]TAGAAAAGAAATAAT	4703
rs561706320	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151577545	ACATCTAGGTCTCGG[A/T]TATCAATGTGAACTC	4703
rs561708515	snp	G/T			missense	NEB	GRCh38.p7	2:151656290	CAGCCGTGACACTGA[G/T]CATGTCGGCAGGGGT	4703
rs561730361	snp	G/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151512667	TCTTAAGGTATTTAT[G/T]AATGGAAGGACTTCC	4703
rs561736266	snp	C/T	0.000399281	0.0141238	missense, intron-variant	NEB	GRCh38.p7	2:151606635	CTCTGGAGGCCTTGG[C/T]GTGCTTGATTTCAAT	4703
rs561747330	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151649278	GCATTATAAAAAGTC[C/T]GTGAGGGGTTAGTTA	4703
rs561766700	snp	C/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151532963	CTAGCAATTCAGCAT[C/G]AAAGTCAAGAGGCGC	4703
rs561767644	snp	A/G	0.000182344	0.00954666	intron-variant	NEB	GRCh38.p7	2:151554032	GTACAGGCGCTGTAA[A/G]GTTAAAATCACATGC	4703
rs561769594	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151556698	CCAACACAGGAGCAC[A/G]CATATTCATAAAACA	4703
rs561771736	in-del	-/AATAGAGACAATACCTA			intron-variant	NEB	GRCh38.p7	2:151653326	TGTAAAAAATTAACC[-/AATAGAGACAATACCTA]AATAGAGACAATACC	4703
rs561773632	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151636551	TTGGGAGGCAGAGGC[A/G]GGTGGATCACCTGAG	4703
rs561806276	snp	A/G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151563253	CTCCTGACCTCTGGT[A/G/T]ATCTGCCTGCCTTGG	4703
rs561859275	snp	A/G	0.00119737	0.0244387	intron-variant	NEB, RIF1	GRCh38.p7	2:151527196	CCTCCTTTTCAGCCT[A/G]GCTGCCAGGACCAAG	4703
rs561865407	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151651520	GATCTATATCTTGCA[G/T]GTGCAGATGGCTAAA	4703
rs561884655	snp	A/G	2.83226e-05	0.00376304	missense	NEB	GRCh38.p7	2:151658084	CCAAGGAAAGTTTGT[A/G]GAGTTTCTGTAAAGA	4703
rs561885346	snp	C/T	1.86524e-05	0.00305382	intron-variant	NEB	GRCh38.p7	2:151619808	AAGCACAAAGGGCTA[C/T]TCCCTGTTGTTCTTT	4703
rs561904743	snp	A/G	0.000197176	0.00992719	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151490498	ATCGTGACTGCTCCC[A/G]GCTCCGGCGCTGAGC	4703
rs561915220	snp	A/G	0.000399281	0.0141238	intron-variant, missense	NEB, RIF1	GRCh38.p7	2:151533479	TAGAGAGCAGTCAAC[A/G]TATCTGGACGCAGAA	4703
rs561926406	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151513696	GCTTATATTCTTTCT[A/G]TAGTAGCATTAAAAG	4703
rs561932473	snp	A/C	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151531587	TTCCCAAAGTGCTGG[A/C]ATTACAGGCATAAGC	4703
rs561965425	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151518608	GTATTGTCCGTTAAG[A/G]TGTAAACACTTAGGT	4703
rs562029680	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151601370	CGCCTTGGCCTCCCA[A/G]AATGCTGGGATTTAC	4703
rs562043011	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151624445	TAAAATAAACCTCCT[A/G]GGAGAAGATAATCCA	4703
rs562061208	in-del	-/GAAC	0.00835141	0.0640778	intron-variant	NEB, RIF1	GRCh38.p7	2:151495666	TACAGTAAAACTAAA[-/GAAC]AACAACAACAACAAA	4703
rs562083839	in-del	-/T			intron-variant	NEB	GRCh38.p7	2:151647116	TACTAAAACTAATAA[-/T]TTTTTTTTTTTGAGA	4703
rs562093491	in-del	-/TGTG			intron-variant	NEB	GRCh38.p7	2:151638836	GTGTGTGTGTGTGTG[-/TGTG]GGTTACCTGGTAGTA	4703
rs562114080	in-del	-/CTT	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151573728	CACTAAGGTAGTATC[-/CTT]CTTCTTCTGAGGTCA	4703
rs562173208	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151547266	TCCATAGCTGTAGAA[C/T]TGTGGCATCCTTCTC	4703
rs562175196	snp	C/T	0.000248523	0.0111445	missense	NEB	GRCh38.p7	2:151554981	CTGTGTTCGGATCAT[C/T]GTCAACACTTCTTGG	4703
rs562182655	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151555133	CTTAATGGGAAAAAC[C/T]CGACTCTGAGATCCA	4703
rs562184453	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151538573	ACTCTGTACAATTTC[A/G]GTAAATCTAAGACTA	4703
rs562190656	in-del	-/G	0.00119737	0.0244387	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151534074	ACGGGCTTTTTGGGT[-/G]GGCTAGACAGATACT	4703
rs562192701	snp	C/G	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151489896	AAAAAAACCGTAATA[C/G]CTAATACTTATAATC	4703
rs562215553	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151683333	ATTTGCATAAGAGGG[A/C]GGTTATTATTTGGAA	4703
rs562216144	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151569699	TTTGGATTTTAAAAT[C/T]TTGGCAACTTAATTC	4703
rs562238211	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151543297	GTTGAACAGATAAAA[C/T]GTAAGAAACACAGGC	4703
rs562247714	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151690183	GCTGTTTTCCCCCGA[C/T]CTTGGCATGACTGGA	4703
rs562250972	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151684040	AAACAAAGCGTAGAT[C/T]GGTGGTTGCCACAAG	4703
rs562252715	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151611887	ATCTGCTCTGCCTAG[A/G]AGAATGTGTGAGGAA	4703
rs562254781	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151722962	CCCTTCCATAACATT[C/G]TTTACTTAATAGATT	4703
rs562257405	snp	C/G	0.00159617	0.0282053	intron-variant	NEB, RIF1	GRCh38.p7	2:151488896	TTGCCATGCTAAATC[C/G]ATATTTTGTATCTAT	4703
rs562274800	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	NEB	GRCh38.p7	2:151735093	CCTATTTAGCACCTT[C/T]TCCCTCCTTAGATAA	4703
rs562276740	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151727527	TATAAATGAATTACA[C/T]AAAAGGAAAATTCAA	4703
rs562328283	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151727397	ATCTGTATTTATGAT[C/T]TCATTATTCTAGATT	4703
rs562338913	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151713549	TTTTTTAAAAAAAAT[G/T]TAGGCTCCAGTTGGT	4703
rs562338944	snp	A/G	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151705884	TATGAGGACACAAAG[A/G]CAGAAGAATGATATA	4703
rs562358079	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151576945	GTTTTCTGTGGCAAG[A/G]GTCTGTGTGGTAGTG	4703
rs562368741	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151641941	TTACGTTAGGTATAT[C/T]TCCTAATGCTATCCC	4703
rs562397367	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151569124	TGATAGCGACAGTAC[A/G]TTTTGAAAAATATAT	4703
rs562419268	snp	C/T	8.28e-05	0.00643375	missense, intron-variant	NEB	GRCh38.p7	2:151614448	AACTTGGTCTTCCAC[C/T]TCTCAAACTCCTTCT	4703
rs562428904	snp	C/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151504666	CCCTTTTATTGGCCA[C/T]AAACTATTTCCCAAA	4703
rs562431197	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151512082	GCTGCCCAGGCTGGA[A/G]TGCAGTGGCGTGATC	4703
rs562443128	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151569502	ATACTCAAGCAGCCA[C/T]GCAGGTAATGTAAGA	4703
rs562445766	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151555999	GCCAAGAATCTTGCC[G/T]CTATAATTTTGTTCA	4703
rs562464958	in-del	-/ATC	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151541281	AACACAACCATAATT[-/ATC]ATGGCCCAAAAGAGA	4703
rs562467957	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151568974	TCATTATGTGTACTG[C/T]AATGCACATTTTTCC	4703
rs562483407	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151620022	GAAATGAAGAGTCCA[A/T]TTACAGTAATAAACC	4703
rs562484158	snp	G/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151518593	GAGGATCCAAGTTCA[G/T]TATTGTCCGTTAAGA	4703
rs562485929	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151635635	CGCTTGACCCCAGGG[C/G]GCAGAGGTTGCAGTG	4703
rs562505444	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151519390	CAAAGGACAGATACT[A/G]TTTGATTCCATTTAT	4703
rs562516214	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151491481	ACATGCACTGAGGCA[A/G]TGAAACAAAATTTTT	4703
rs562521752	in-del	-/A	0.00159617	0.0282053	upstream-variant-2KB	NEB	GRCh38.p7	2:151735073	CCAAGAGGGTATACC[-/A]AAATCCTATTTAGCA	4703
rs562522818	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151628071	AGTCTAATGGGAATA[A/G]TCCAGTGGGAAGACA	4703
rs562556217	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151639581	CTAATAATCTGAAAT[C/G]TATGTTAACAAAAGG	4703
rs562603844	snp	A/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151548557	AAAAGTCATTGACAA[A/T]ATTTCAATATTAATC	4703
rs562610622	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151675608	ATCCTTAAGAAAATA[C/G]AAATTGTTCACTGCC	4703
rs562628217	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151731006	ATGAGAAATATCATT[C/T]GGACACTAGAAAATA	4703
rs562629326	snp	A/G	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151667693	CCACCACATCTGGCT[A/G]ATTTTTTTTTTTATT	4703
rs562632547	snp	A/T	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151656923	TCAGTCATTTACTGA[A/T]GAGAAAAGTTTCAAT	4703
rs562634452	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151664074	AATAATCTCAGAGTT[A/G]ATCGAAGAGATGTGT	4703
rs562646640	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151498464	TAAGTTAGAGGAAGA[A/G]AAATACCAGAAGCTT	4703
rs562666913	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151531989	ACCAGAGTGGGAGAT[A/G]GTATCTAGCTTTCTC	4703
rs562669490	snp	A/G	4.97673e-05	0.00498811	missense, intron-variant	NEB	GRCh38.p7	2:151614302	GGTCATAGGCCTTCC[A/G]AGCCTGAATGACGTC	4703
rs562682807	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151620720	GATCAAAAATAAGGA[C/G]TCAAATGAGCCACAT	4703
rs562717514	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151509968	ATTATCACCAGGCCA[A/G]CTCAAAATTACAAAG	4703
rs562729009	snp	A/T	0.00478085	0.0486577	intron-variant	NEB	GRCh38.p7	2:151549533	CATTCTATCAGGTTG[A/T]ACCTTGAGGGTGAGA	4703
rs562733275	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151696788	CCTGTCAGATCCAAG[C/G]TGGCCCACAGGCCAA	4703
rs562737744	snp	C/T	0.00358779	0.0422022	intron-variant	NEB	GRCh38.p7	2:151688933	GTTTGTTTCTGGAAT[C/T]TTCCACTTCATATTT	4703
rs562747897	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151619203	GATTCAAACAAAGGA[A/G]GCCTGAATCCCTAGG	4703
rs562756150	snp	C/G	0.00279162	0.0372561	intron-variant	NEB, RIF1	GRCh38.p7	2:151531444	GCCTCAGCCTCCTGA[C/G]TAGCTGGGACCACAG	4703
rs562766815	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151658727	AAAGGCTTGATGGAA[A/G]GGCTGTCTAAGAACG	4703
rs562779765	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151576656	CCTGCCTCAGCCTCC[C/T]GAGTAGTTGAGACTA	4703
rs562792360	snp	C/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151530940	CAGGGTTTGTTACAT[C/T]TCATTAGAAGGAGGC	4703
rs562819573	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151505199	ATTTTACTTTGGAAA[C/T]GAATGGCATGATAAT	4703
rs562828540	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151674802	ACACATATTGAAGAG[A/G]GGAATATTGAAAGAC	4703
rs562842160	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151611794	GCTATGAAACACTAT[A/G]TGTATCCCAGCCCTC	4703
rs562850745	snp	G/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151497137	AAGACAAAACACAGT[G/T]GTCCAAGGAGCCAGA	4703
rs562873882	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151611175	TGGATCTCAGTTATG[C/G]AACTATGAGACAGTA	4703
rs562906648	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151641102	TAAGTACCGCAGATT[C/G]AATAAAAATTATCTT	4703
rs562911495	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151649158	TTTGTTGTTTTCTCA[C/T]TTTGTTGGATTCTGT	4703
rs562919926	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151704722	CCTGCTTCGGCTCAC[C/G]CACAGTGCGAGCACT	4703
rs562928562	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151710235	AGAAATAATGGCATG[C/T]GGCCAAAATAATATT	4703
rs562966880	in-del	-/TGTT	0.00279162	0.0372561	intron-variant	NEB, RIF1	GRCh38.p7	2:151494972	GTTTTTTTACTGGAC[-/TGTT]TGTTTTGCAGCACTT	4703
rs562985649	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151495597	ACAACCATATATAAT[A/G]TCACAGAGCACAAGC	4703
rs562995819	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151704944	CACGTCCTTAGTAGC[A/G]GAGATTCTTGTGTAT	4703
rs563001387	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151553697	AGCTCTGAAGTCAAG[C/T]TGGACAAATGGACAT	4703
rs563012644	snp	A/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151718722	TTTCTCACAACCCCA[A/T]ACTCTCCTTCTTCAT	4703
rs563060192	snp	G/T	3.40263e-05	0.00412456	intron-variant	NEB	GRCh38.p7	2:151568467	TTACTTGTTAAGAAA[G/T]CATCATGTTGTCCAA	4703
rs563085264	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151733805	TCAAACCTGAAAAAT[A/T]ACAAAGTTGTAAAGC	4703
rs563123280	snp	A/C			intron-variant	NEB, RIF1	GRCh38.p7	2:151502618	ATGTTTTAGAGAAAA[A/C]ACAGTTAAAATTTCA	4703
rs563153373	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151695256	GGAATAAATGAATTA[C/T]ATATAATTTAAATGA	4703
rs563158387	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151521980	GTAATGTAGTAAAAC[C/T]ACATACACTTGGCAT	4703
rs563162141	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151528957	CCCATTTCTCAGCCA[C/T]CCACCGCAAAAGCTG	4703
rs563169928	snp	A/G	0.0298908	0.118541	intron-variant	NEB	GRCh38.p7	2:151698765	GCCTCAGCCTCCCGA[A/G]TAGCTGGGACTACAG	4703
rs563172875	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151600959	ATTGAGAGCATCTCT[G/T]AGGCAAGAACTGTGT	4703
rs563173814	snp	C/T	3.14747e-05	0.00396691	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151490429	GGTGGTGGTCTGGTG[C/T]TTCTGAATGCTCAGA	4703
rs563178837	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151614741	TTAAAAGTCAAAACC[C/T]GAACCTAGCAGGGGT	4703
rs563192073	snp	G/T	1.71581e-05	0.00292895	synonymous-codon	NEB	GRCh38.p7	2:151655315	TTGTAAAATATCTGG[G/T]GTATCAGGCATCACA	4703
rs563195889	snp	A/G	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151575592	GTCTTCCCCTGTTGC[A/G]GGAAGTCAGGGACCG	4703
rs563198994	snp	C/T	0.00119737	0.0244387	intron-variant	NEB, RIF1	GRCh38.p7	2:151528363	ACATGCTTTTATGTA[C/T]ACTATTTAATAAGGT	4703
rs563201773	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151542543	GATATCCCAGTTACT[C/T]GGGCCAGAAACTTGG	4703
rs563211185	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151593581	ATTTTAGGAGGTAAA[C/G]AACCTTAGATGTATG	4703
rs563224214	snp	G/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151493152	AATGTAAAAGCACAG[G/T]TAATGTCTATTTTAG	4703
rs563226332	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151670131	TGAGAAGTGACATCT[C/T]GCTCAGTACAAAAGA	4703
rs563228394	in-del	-/TGTA	0.00239856	0.0345474	intron-variant	NEB	GRCh38.p7	2:151660370	GTGTGTATGTATGTA[-/TGTA]TGTATGTATATCTTT	4703
rs563230733	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151648260	TCCCTTTGAGGTATG[C/T]AGCATGAGATGTGTG	4703
rs563238012	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151609081	ACTGGAAATCCCTTT[A/T]GTGATCATAAGTTGA	4703
rs563239607	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151652429	AGAGTCTCACTACGT[C/T]GCCCAGGCTGGTCTT	4703
rs563241688	in-del	-/ATG			intron-variant	NEB	GRCh38.p7	2:151611656	TTTTGGATGAAACAA[-/ATG]ATCATCTATCTTGTG	4703
rs563247822	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151686163	TGAAGAAATTGTTGT[C/T]ACTGTTTTGTTCATG	4703
rs563268864	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151707916	AGTAATGGGAGACTC[A/G]GATCACTTTTCCACC	4703
rs563269120	snp	A/C/G	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151493710	CTGTAAGATAAATTA[A/C/G]TGGTACAACCATGTT	4703
rs563277006	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151615628	TTGGCTGTTTCTCAC[A/G]TATTATTTAAAGGGA	4703
rs563284532	in-del	-/AGGGCTG	0.00636936	0.0560724	intron-variant	NEB, RIF1	GRCh38.p7	2:151509028	GAAGTTTTAGTTTGT[-/AGGGCTG]AGGGCTGAGGAATGA	4703
rs563314229	in-del	-/AA	0.00159617	0.0282053	intron-variant	NEB, RIF1	GRCh38.p7	2:151487500	TTGTTCTTTCCATTT[-/AA]AATATAGCTTGGAAG	4703
rs563317498	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	NEB	GRCh38.p7	2:151735212	GCAACGTGTGAATGC[A/G]GACACAAACAGGCTC	4703
rs563318828	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151671741	GTCCACCTAGGCTAT[A/G]CTTGAGCTCATCTGG	4703
rs563322824	snp	C/T	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151543314	TAAGAAACACAGGCA[C/T]ACACATCAATTTCTT	4703
rs563331627	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151707139	AAACAAAATACTCAT[A/C]GTAACTCTTAAAAGC	4703
rs563334086	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151636752	TGCCAATGCACTCCA[A/G]CCTGGGCAACAAGAG	4703
rs563351070	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151673305	AACTGTTATGCAAGA[A/G]AATTCAAATCCACTT	4703
rs563374542	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151550552	CAGAAAGGGAGGACA[C/T]GGAGGAGTGTCTGTC	4703
rs563381877	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151710013	CCAAGAAAGATCTCT[C/T]AAGGGCCAGGAGCAG	4703
rs563400410	in-del	-/T	0.0946579	0.19588	intron-variant	NEB	GRCh38.p7	2:151664023	CTCTTTTTACTTCAT[-/T]TTTTTTTTTCCCGAG	4703
rs563401255	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151645113	GTGTGCCTTTGTTGG[C/G]CAAACTGTTGTTATA	4703
rs563430718	snp	G/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151577589	GCTGTCATGTTTTTT[G/T]TTTGCCTTTGAGACG	4703
rs563433708	snp	A/G	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151487209	CATCTTTCACTCTGG[A/G]AATTTGGGAGCATAC	4703
rs563449440	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151573045	ATGAGTCACTTTAAC[A/G]TGAATTTGCTTTGTT	4703
rs563487406	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151686028	AGACCCTGGTTTATA[A/G]AAATAAAGTATGCAA	4703
rs563488101	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151638730	GATTCTGGAATGATG[A/G]CACGTGGCCCTGTGC	4703
rs563500961	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151506705	TAAAAATAAAAGTTA[C/T]GTTGTTAGCAGATTT	4703
rs563513307	snp	A/C	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151520224	TGTTAAATTAGGAGA[A/C]TTTATTGTTATTTTA	4703
rs563522035	snp	C/T	2.49106e-05	0.00352912	missense, intron-variant	NEB	GRCh38.p7	2:151630804	TGTCTTTGTCCCAGG[C/T]CTCTGTGTATAAACG	4703
rs563560112	snp	A/G	0.000132483	0.00813782	missense, intron-variant	NEB	GRCh38.p7	2:151643220	AGGCTGGAAAACTTA[A/G]ATTGATCTGGGTGCT	4703
rs563567747	snp	A/G	0.00557542	0.0525036	intron-variant	NEB	GRCh38.p7	2:151702221	TTTGATTGCACTGTG[A/G]TCTGAAAGATAGTTT	4703
rs563594942	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151637280	GTTAGACTTTGAGCA[C/G]AGTTTCAGTAGACTA	4703
rs563595055	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151629698	TTGACATCAACAATT[C/T]AGAGATTATTAAGTG	4703
rs563610639	snp	A/G	0.00557542	0.0525036	intron-variant	NEB, RIF1	GRCh38.p7	2:151486680	TAGTAACAAGAATGG[A/G]GTAGTAACAAGAATG	4703
rs563635709	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151691051	AGCAACTCAGCAACC[A/T]GATTAACCTTACCCT	4703
rs563649839	snp	G/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151527426	TAAATAATTATTCAT[G/T]GTATTTCTCAGGTGC	4703
rs563671419	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151651370	AAATGATAATCCTTA[C/T]GGGCTAAATGGCAGA	4703
rs563691738	snp	A/C	0.000496656	0.0157506	missense, intron-variant	NEB	GRCh38.p7	2:151643909	TAGTTCTTGTAGTCC[A/C]CGTCGCTGACTAAGG	4703
rs563696157	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151652039	CTGAAAACAAAGGAG[A/G]GCAAATATGAAAATG	4703
rs563706819	snp	A/G	0.00358779	0.0422022	intron-variant	NEB	GRCh38.p7	2:151684690	AATGCAGATACCTCT[A/G]AGAAGTGCAAAAACC	4703
rs563712566	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151722002	CAGGTGATATGAAGA[A/G]GGTGGCGTTAAAAAT	4703
rs563727665	snp	C/G	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151532665	AAGCTCTTAATTGGA[C/G]CTTAACCTCCTCATT	4703
rs563754609	snp	C/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151506546	CAACAAAACCCTCCC[C/G]ATATGTAACACAAAA	4703
rs563768825	snp	G/T	1.65941e-05	0.00288041	synonymous-codon	NEB	GRCh38.p7	2:151541513	AGGAACTGAAGTAAA[G/T]ATTGACTTCTGCTTC	4703
rs563798779	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151562338	GGGTAGGCCTCTCAC[C/T]AGCTGGAAGGTCTTT	4703
rs563800224	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151650004	CTGACCCATTTTTAC[A/G]TGATTCAGTGTAGGA	4703
rs563821589	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151670848	TCATCTCCCTGTTTT[C/T]CCCATGTTCAAGATC	4703
rs563831189	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151577110	CTTTCTAGTAAGTTC[C/T]CTACACAGCAGCCAG	4703
rs563836738	snp	C/T	6.64033e-05	0.0057617	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151618428	TTCCAAGGAATCAAT[C/T]GGAACCCAGCCAATG	4703
rs563840333	snp	A/G	4.97162e-05	0.00498554	intron-variant	NEB	GRCh38.p7	2:151563600	TTAAAGTGGACATTT[A/G]CTTACCGCACTCCTC	4703
rs563860152	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151536391	CTAGTTTATTTCTAT[A/G]TATTATAATTATTAT	4703
rs563860284	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151671416	TTGTTAGAGTGCATT[A/G]TACAACACAGAAGGG	4703
rs563860375	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151664258	CATTTGCTTAGGATT[A/G]TAAGTGATTTGAATA	4703
rs563875345	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151729004	CATCCATATCACTGT[C/T]TGTCATGCTCAAAGA	4703
rs563892367	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151714457	GCCAGGATCCAAGTT[C/T]ATAGTCTTTCTGTAA	4703
rs563896790	snp	C/T	0.00932926	0.0676579	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151514390	TTCAGTGAGGCCCTT[C/T]CCACGGATGCTTTCC	4703
rs563910276	snp	C/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151513508	CAATAAATCAGATGA[C/G]AGAGGGACACTTTAT	4703
rs563918991	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151678900	GGACATTTGTTATTC[A/C]ATCATCACATATTTA	4703
rs563925147	snp	C/T	0.00358779	0.0422022	intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151507202	ACTAATTTTAAAAAA[C/T]ATATAAAGCTAGGGG	4703
rs563934691	snp	A/T	2.32783e-05	0.00341154	missense	NEB	GRCh38.p7	2:151691940	TAGCATTTTCCTTTA[A/T]CTTCTTCATATTCTG	4703
rs563947796	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151556888	AGAGGGAAATTTATA[C/G]CACTAGATGCCCACA	4703
rs563983531	snp	C/T	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151564032	CATGTATGTTCAAGG[C/T]AAGGCTGAAATCTTT	4703
rs563984509	snp	G/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151509253	TTTTCGGAAGAAACG[G/T]TAGTTCATCATGAAC	4703
rs563991393	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151549812	AGCTTAACAAATCAC[A/G]TATAGCTCATGTTAC	4703
rs563992275	snp	A/G	0.00119737	0.0244387	intron-variant	NEB, RIF1	GRCh38.p7	2:151533652	GATGTAGGCATACAC[A/G]CTTTATGTACTCACA	4703
rs564017545	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151641471	GAGTAGCTAGCACTA[C/T]AGGCATGCGCCATCA	4703
rs564034546	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151571178	GCCCAGCTAATTTTG[C/T]ATTTTTAGTAGAGAC	4703
rs564045842	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151615476	CTGCTTACTTTGCCA[C/T]TTGTTCTTGTGTCCG	4703
rs564051788	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151714344	CAGACTTCACCCCAG[A/G]CTATTGTATGTTCTT	4703
rs564052640	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151505955	ACAAGCCTCTCTGTT[C/T]TTCAGATCTAATCTC	4703
rs564102266	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151521312	CATGCAGAACAGTTC[A/G]GCATGATGCAGGCAC	4703
rs564138223	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151550445	TCACGAAGATATAGC[C/T]AGGCACATGTTTGTA	4703
rs564153904	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151721999	TTGCAGGTGATATGA[A/G]GAGGGTGGCGTTAAA	4703
rs564164306	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151676621	TTTCCTACTGCTGTT[A/G]TATTGTTCATTCCTT	4703
rs564174822	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151557525	TCATTTTATGAGGCC[A/G]GCATCATCCTGATAC	4703
rs564212448	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151721903	TATTTCCTAACTTAC[C/T]TGTGGAAGGATACGA	4703
rs564219539	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151658145	TGAAAGCCTGGATTT[A/C]TTTTAGAAGAGTAAA	4703
rs564221677	snp	C/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151491344	AGAGCTCAGGAAGTT[C/G]CTACAGGTCAAATCC	4703
rs564222446	snp	A/C	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151578119	TACCTCTGGAAGCTT[A/C]AGGGAACCAAGGTCA	4703
rs564226824	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151617717	ATAGGAAAGAGTTAT[A/G]GCACACAGTATTTTT	4703
rs564241582	snp	A/G	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151486638	CATAAGCAAGATCTG[A/G]TATATCCATACAGAT	4703
rs564250981	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151630040	AATATCTATCTATAC[A/G]TATAAAAATATATTT	4703
rs564255340	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151651560	ATATGTTAGATTAGG[A/G]AGAAAATTCCACAGG	4703
rs564265023	snp	C/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151578678	CAAGGAGGGAAGGAG[C/G]GAAGGAAGGAAGGAA	4703
rs564270527	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151685826	CATCCTAGTTTCCCA[C/T]GGTCACATATGTGTT	4703
rs564277371	in-del	-/TGTATGTATGTA	0.00438857	0.0466372	intron-variant	NEB	GRCh38.p7	2:151660359	AAACATATTCTTGTG[-/TGTATGTATGTA]TGTATGTATATCTTT	4703
rs564289152	in-del	-/CTAT	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151564706	GGTAGGTGCTCAATG[-/CTAT]CTATGTGCCCCCAGA	4703
rs564295966	snp	G/T	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151698582	TTTCTGATTTCTCTC[G/T]TAGCATGTTTTCAAG	4703
rs564304837	snp	C/T	0.000115924	0.00761239	missense, intron-variant	NEB	GRCh38.p7	2:151644077	TCATCTTCAATGTTC[C/T]GGGCACCAATGTGGT	4703
rs564320646	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151526510	TACGTTCACAGCACG[C/T]TCAGATATGCCATTT	4703
rs564325749	snp	C/T	0.00180231	0.0299651	intron-variant	NEB, RIF1	GRCh38.p7	2:151512720	TGAGTGATGGCATGA[C/T]GAATGTCCTTACCTG	4703
rs564357294	snp	C/G	0.00279162	0.0372561	intron-variant	NEB	GRCh38.p7	2:151707807	ACTCAGAAAACAAGG[C/G]AATCAGCTTGGTATC	4703
rs564360823	snp	A/G	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151636708	ATTACTTGAACCTGG[A/G]AGGCGGAAGTTGCAG	4703
rs564376832	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151705828	ACTCAGGAATGAAAA[A/G]CCAAATATCATATGC	4703
rs564383442	in-del	-/TTTCT	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151731337	CCTTGCTTCTCTCTC[-/TTTCT]TTTCAAGTTTAAGTT	4703
rs564400584	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151519520	TTATAGTTTCTGTTG[A/G]TATGAAAACATTTTG	4703
rs564403179	snp	C/T	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151551379	CAGGTGGGATCCAGG[C/T]TCTTTCTCTTCTGAA	4703
rs564409665	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151607314	CTAGGCACCCACCGA[G/T]GTATCCAAGCACTCA	4703
rs564417486	snp	C/T	0.0174175	0.0916809	intron-variant	NEB	GRCh38.p7	2:151605396	AGAGTACTGAAGGAA[C/T]CTCAGGTAGGGAGAG	4703
rs564453666	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151656858	AGATGAAAAAAAAAA[A/G]GCAAAAAAACAGAAC	4703
rs564490447	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151623476	CATTTTTATACCCCA[C/T]TCTCAAATTAGATTG	4703
rs564497323	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151704824	TCACCCGTCTTCTGC[A/G]TCGCTCGCTCACGCT	4703
rs564504601	snp	C/T	3.31296e-05	0.00406985	missense, intron-variant	NEB	GRCh38.p7	2:151629574	AGGCCTTGGCAGCCA[C/T]GATGGGGATGGCGTC	4703
rs564509638	snp	C/T	1.65616e-05	0.00287759	synonymous-codon	NEB	GRCh38.p7	2:151697410	ATCCTCGAAGCTGCC[C/T]ACATAATGTCCCAAA	4703
rs564510167	snp	A/G	1.65778e-05	0.002879	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151650328	CCTCTAAAGAACCCA[A/G]GGGACTCCATCCTAT	4703
rs564530918	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151639615	ATGAGAATAAGCATA[A/T]TTTATGCAGACTATT	4703
rs564543405	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151540609	ACCATTTATAGTAAT[A/G]AGCTCTCTGATCAGA	4703
rs564572990	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151677041	TCATGGACAGGCAGG[A/C]AAACGATACACACCT	4703
rs564576692	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151531624	GCCCGGCCACAACAA[C/T]TCTTTATTGGGGAGG	4703
rs564635324	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151684643	CATGCTCTTATAGAA[C/T]CACAAGGGTCGTTTG	4703
rs564636113	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151601468	AAAATGTGTAACCCT[A/T]TCTACGTGGAAAAAA	4703
rs564643938	snp	C/T	6.6201e-05	0.00575292	missense, intron-variant, utr-variant-3-prime	NEB, RIF1	GRCh38.p7	2:151497634	AAAGTACCGAGCTAA[C/T]ATTTTCTTGATTGTG	4703
rs564645145	snp	A/G	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151522505	CCATCTCTGAGTCTA[A/G]TCTACCTTCCTATTC	4703
rs564675123	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151721272	TATCATGCTGTTTTC[C/T]GCTCCAAAATCTTAT	4703
rs564680867	in-del	-/AG	0.00199481	0.0315187	intron-variant	NEB, RIF1	GRCh38.p7	2:151520846	TCCATCGTGGGCAAC[-/AG]AGCAAGACCCTGTCT	4703
rs564725049	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151520055	AAAAAAAAAAAAAAA[C/T]GGAAAAGGCTTCAGG	4703
rs564732735	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151647292	TTTTTGTATTTTTAG[A/T]AGAGATGGGGTTTCA	4703
rs564744440	snp	C/G	0.00398564	0.0444627	intron-variant	NEB	GRCh38.p7	2:151690971	CTCACTTCTCTGTCT[C/G]TCTCTCTCTCTCTCT	4703
rs564752449	snp	C/G	1.68148e-05	0.0028995	synonymous-codon	NEB	GRCh38.p7	2:151570264	CCATTTGGCCCAGTC[C/G]AGCCGGTACTCTCGT	4703
rs564755487	snp	C/T	1.75348e-05	0.00296093	intron-variant	NEB	GRCh38.p7	2:151633629	TATTTCTATGCACAG[C/T]TCCATTTATAGATGC	4703
rs564759053	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151636019	GGTTGACCAGTTTTC[A/G]CAGAAGACGCTGTGT	4703
rs564761820	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151509223	CATCTAAATGGAAGC[A/G]AATTAAAGCCAGATT	4703
rs564794233	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151632806	AATCCAGAGAAGGTG[C/T]CCAACAAATAGACAG	4703
rs564853737	in-del	-/T	0.00318978	0.0398085	intron-variant	NEB	GRCh38.p7	2:151689973	CCTATCTTGAGAAGG[-/T]ATGTACTACTCTCTA	4703
rs564867595	snp	A/G	0.00394874	0.0442581	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151579389	CACATCATTCTGGTC[A/G]GGAAAGCAAGACCAG	4703
rs564867769	snp	A/T	0.00159617	0.0282053	intron-variant	NEB, RIF1	GRCh38.p7	2:151494859	TTCACTATGTTGGTC[A/T]TGCTGGTCTTGAACT	4703
rs564869163	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151693722	TGAATATATGTGTTC[A/C]TATATATTTATAATA	4703
rs564871448	snp	C/T	0.00279162	0.0372561	intron-variant	NEB	GRCh38.p7	2:151678882	AGGGGCATTTCAGAA[C/T]GAGGACATTTGTTAT	4703
rs564874548	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151529429	AATGCTCCTTAAGAC[A/G]GAATTTTAAAAATCT	4703
rs564889467	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151529616	GCTCACTGCAACCTC[C/T]GCCTCCCAGGTTCAA	4703
rs564907904	snp	C/T	3.32497e-05	0.00407722	intron-variant	NEB	GRCh38.p7	2:151687567	GCCAGATCCCACTCA[C/T]CAGGAAATGTCCCCA	4703
rs564923917	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151529086	TTCATGCTCCTGGGG[C/T]CTGACTCTTGCTTTG	4703
rs564925756	snp	A/C	0	0	intron-variant	NEB	GRCh38.p7	2:151536370	GGCAAAAATTTAAAT[A/C]AATGTCTAGTTTATT	4703
rs564932879	snp	A/G	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151516739	TGTTGTCTAGGTGTT[A/G]AGGGGATGGGTACCA	4703
rs564961541	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151634372	AATGAGGCTGGGCAC[A/G]GTGGCTCATGCCTGT	4703
rs564969085	snp	C/T	0.00557542	0.0525036	intron-variant	NEB	GRCh38.p7	2:151714213	GAAGAAAACAATTCC[C/T]TCTGACCCCTTCCCT	4703
rs564980806	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151558816	AAGATGGACTAAAAA[A/T]GTACACATAAGACCT	4703
rs565002768	snp	A/C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151680913	AAATTTATTTTGAAG[A/C/T]GAAAAGGAAGAGTTT	4703
rs565012000	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151686075	CAACAACATTGAAAA[A/C]AACAGTTTGTCTTCG	4703
rs565023747	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151653843	CAGTGAAAGAGAAGA[A/G]TGAACTCCGGATAAA	4703
rs565039008	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151581674	AGTCATAAAACATAC[C/T]TGAATAAATGGATGA	4703
rs565055664	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151574578	TTTTCTTCTTGTTCT[A/G]TGGCACTATTAGGTC	4703
rs565070678	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151626677	GAGTAGCTGGGACTA[C/T]AGGCGTCTGCCACCA	4703
rs565107060	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151617790	CTTTAGGCTGGGCAC[A/G]GTGGCTTACACCTGT	4703
rs565114531	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151669356	GTGGTAAGTTCTGTG[C/T]TTAAAGAGGTGAGGA	4703
rs565119047	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151623939	CTTCAAAGGAGAGAA[C/T]ACTTTTAGCTATCAT	4703
rs565122954	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151575607	GGGAAGTCAGGGACC[A/G]AGTCCATCTTCCCTC	4703
rs565124435	snp	A/C			intron-variant	NEB, RIF1	GRCh38.p7	2:151495222	CAACCTCGGTATCTC[A/C]CCTCAGTGTCATTCT	4703
rs565131674	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151674323	AGAACCACAAAAATG[C/T]TTCTAAAAGTGACAG	4703
rs565135862	snp	G/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151523184	TCCACTGTTTTTTTG[G/T]TGGTGGTGGTGATCC	4703
rs565153313	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151560445	AGACTCTAATGACTG[A/T]GCATTTGGAATTATT	4703
rs565162006	snp	C/T	0.000379706	0.0137735	synonymous-codon	NEB	GRCh38.p7	2:151567462	TTTTTGCTTCACATG[C/T]TCAGCTTTGTATTTC	4703
rs565184120	snp	C/T	0.000161335	0.00898006	missense	NEB	GRCh38.p7	2:151672385	TCACTCTGAATTTGA[C/T]TGACATTCCTCGTAT	4703
rs565189262	snp	A/C			intron-variant, utr-variant-3-prime, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151497800	GGATGAGGAAAAAAC[A/C]CAGTCATCCAAGGAG	4703
rs565241507	snp	C/G	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151559423	AAATACCATTTGACC[C/G]AGCAATCCCATTACT	4703
rs565248569	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151730605	ATGAAACACTTGGCT[A/C]ATTTCTTAGTGAAAA	4703
rs565264927	snp	A/T	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151631624	TATCATAATTATAAC[A/T]TCCCTATGCAGGGAA	4703
rs565292161	snp	A/C/T	4.15533e-05	0.00455795	intron-variant	NEB	GRCh38.p7	2:151672323	AGCGAGAAGTGATCA[A/C/T]CCTTTAAGTGCAAAC	4703
rs565299814	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151638573	AAGCTTTCTCATAAA[A/T]TTTCCAGAACGAATG	4703
rs565333645	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151513766	ACATACAGGGTGAAT[A/G]TAAATCCACATAACA	4703
rs565335470	snp	A/G	0.00199481	0.0315187	intron-variant	NEB, RIF1	GRCh38.p7	2:151522068	TGCCATGTCTCGGCA[A/G]GTGGCAGCCCCCGGG	4703
rs565336554	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151638007	AGCCAGGTGAAATAA[C/G]TAACACATCAGCTGA	4703
rs565342176	snp	C/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151521826	TGCAGCTTTTTACAA[C/G]TACTAATATGAATCT	4703
rs565372251	snp	C/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151521403	TGAAAAAGTTTCACT[C/G]TCAACATAAAGAAGT	4703
rs565400770	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151572378	AATAGTTAATGCAAA[C/T]GTGTATTATGTTATC	4703
rs565431433	snp	G/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151494519	GAAACCACCATCATT[G/T]TACCGCTAGTCTCTC	4703
rs565433415	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151715852	CTGGAGAGTGTAGCA[C/G]TAAACCAACTGGCAA	4703
rs565435272	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151659868	TCATTTTTAGAGCTA[C/T]GTAGTATTTCATTAG	4703
rs565437315	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151666826	CTCAGCTTCCCAAAG[C/T]GCTAGGATTAGACGT	4703
rs565466689	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151500666	CAGTGGCACAATCAC[A/G]GCTCACTGCAGCCTT	4703
rs565467379	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151652568	ACAGAATTTTGGAGA[C/T]GGAGAGAAGGTAGGA	4703
rs565486015	snp	G/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151659813	AACTTAATAATATAG[G/T]TTAGACATATTTGAA	4703
rs565504789	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151544528	GGTGATTCTCATACT[A/G]AGCCAGAGTGGAAAA	4703
rs565538052	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151555539	CTTTCAAAAATACAG[C/T]GCAATCAACTTCTGT	4703
rs565559334	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151672746	CGCTGCAATTACATT[A/C]ACATATAAAGACACT	4703
rs565580426	snp	G/T	0.000399281	0.0141238	missense	NEB	GRCh38.p7	2:151551776	GAAGGGCCCGGTCCA[G/T]ATCCACGGTTTTGGT	4703
rs565598716	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151514615	GAAAGCTTGAAGTTA[A/G]TAGAATGCTAAGGTA	4703
rs565601680	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151557143	AATAAAGAAGAAAAG[A/T]AAGAAGAATCAAATA	4703
rs565633504	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151578882	CGGTCAGGAGTTCAA[A/G]ACCAGCCTGGCCAAG	4703
rs565642365	in-del	-/GTCTTC	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151575577	GGGTGACCACAAGGA[-/GTCTTC]CCCTGTTGCGGGAAG	4703
rs565647243	snp	A/G	3.31235e-05	0.00406948	missense	NEB	GRCh38.p7	2:151672481	GTAGCGACATCCTGG[A/G]CCATCTTTGCAGCTG	4703
rs565651664	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	NEB	GRCh38.p7	2:151736454	ACACATCTCAATATC[C/T]TTAGGGATTATTAGA	4703
rs565666640	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151638394	ATGTGAGGAATGCCC[C/T]GCAGCTTGGGATATT	4703
rs565679431	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151692560	ATCTGCTAATAATCA[G/T]GAAGATGTTTATGTT	4703
rs565700705	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151716032	AAAATAGATTCCTTT[C/T]TCTTTCTAAATGACC	4703
rs565700902	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151721408	CATTCATTTTCCTTG[C/T]CCCTCAAAACTCAGA	4703
rs565728404	snp	A/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151508525	AGCTGGAGGGTTAAG[A/T]GTCAAAGACATGACC	4703
rs565730899	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151698866	GATGGTCTCCATCTC[C/T]TTTTTTTTTTTTTTA	4703
rs565737442	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151722027	AAAAATTAGACCTCA[A/G]AAGTTGGAGACACCA	4703
rs565759383	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151631863	AAGAGTGGGTTTTTC[C/T]AGTGGTTGGATTGTT	4703
rs565775242	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151571763	ATAACAGAGAGACTC[A/G]GAAATAATAGTAATT	4703
rs565776982	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151729742	ACCACTTAGGTGACT[A/G]CACTAGCTCGGTTGA	4703
rs565778338	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151533823	AAAAGAAGACATCTT[C/T]GGAATAGAAAGATAT	4703
rs565797221	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151629087	CCAAAAAAAAATGAG[C/T]TGGCAAAAACACAGA	4703
rs565808934	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151486145	ATCCAGAACATATGA[C/T]GAACTCCTACAACTC	4703
rs565823706	snp	C/T	0.000399281	0.0141238	missense	NEB	GRCh38.p7	2:151727795	TCCTCTCCACCGGCT[C/T]TGCTGATGCTGGCTG	4703
rs565857707	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151500896	GAGCCACCACGCCTG[A/G]CCCCAAATAAGATTT	4703
rs565862415	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151616828	CTGTTTTATGAAAAA[C/T]TCAATGCATTGTGCT	4703
rs565866686	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151625425	TAAATGGCATAAAAA[A/G]CCAACTAAGCTAACT	4703
rs565867868	in-del	-/T/TT	0.000129554	0.0080475	intron-variant	NEB, RIF1	GRCh38.p7	2:151516444	TGTTGTGTGGTGTGG[-/T/TT]TTTTTTTGACTTACC	4703
rs565869762	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151507797	CCCAATACCACCAAC[A/G]AAGTAACAGATGAGT	4703
rs565902147	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151624551	ATCAGGCTTGTCCTT[C/T]GGTCTGTTTTATAAT	4703
rs565924213	snp	C/T	1.65622e-05	0.00287764	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151631227	CAGCTTGTCCGGAGG[C/T]TGGCGGTAGATGTTA	4703
rs565937163	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151679608	AATAGTTTTCAATCA[A/G]ATTTGCTTCCAATTG	4703
rs565944075	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151505713	ACTTAGTGTGAATGG[A/G]ACCTCATTCTGATAC	4703
rs565945220	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151559033	AAAAAATTTCTGCAA[C/T]CTATCCATCTGACAA	4703
rs565959687	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151605297	TATTAACATATATTC[C/T]AGATGGGGAAAACAA	4703
rs565968165	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151730175	AATTATTCCTATACC[C/T]TCCTGATTAGTAAGT	4703
rs565998554	snp	C/T	0.000100455	0.00708641	synonymous-codon	NEB	GRCh38.p7	2:151565525	ATTGACAGAATTAAT[C/T]TTGGCTAAAACAATC	4703
rs565999392	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151512425	CAACCGCCTGGGCTC[A/G]ATTGATCTTCCCACC	4703
rs566010204	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151730741	ATTTCCCTCAATGGC[C/T]TGCATTCTTTTCAGT	4703
rs566036465	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151556424	TAAATTTCCCACTGT[A/G]AGTCATGGTCAAAAC	4703
rs566056296	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151506095	CAGAGGCTTTGAGTG[C/T]AACTCATAGGTCATT	4703
rs566059908	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151498965	ATAAGAAACGAGGAT[A/G]ATAGTCGGATCTTTG	4703
rs566080141	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151623045	GAAGTTGAAGCTATG[G/T]TAACTGATTTACTTA	4703
rs566087290	snp	A/T	0.00478085	0.0486577	upstream-variant-2KB	NEB	GRCh38.p7	2:151736015	CATTGACCTTCTTAG[A/T]CATTTTTAAGTTTCA	4703
rs566096042	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime, intron-variant	NEB, RIF1	GRCh38.p7	2:151485703	TGGAGAGTCTAAACC[A/G]AAACATTGACTGCAG	4703
rs566125535	snp	A/C	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151636799	AAAACAAAACAAAAC[A/C]AAAAAAAAAGATACC	4703
rs566144499	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151676569	TTACTAATCAGGTTA[C/G]AATCCTGAACCTTTT	4703
rs566149448	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151606852	TTCTGGGTTCTTTTC[A/G]TTGTTGGATATTTCC	4703
rs566158320	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	NEB	GRCh38.p7	2:151735277	TCAGTAACTTATCAG[A/G]AGAAAATAATGCCCT	4703
rs566164056	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151609720	TTGTGCAGTGCACAG[C/T]CCAGGGGACTGTCCT	4703
rs566181075	snp	G/T	0.00318978	0.0398085	intron-variant	NEB	GRCh38.p7	2:151677429	TACACATAACTGTAA[G/T]TTTTAAAAAATTAAA	4703
rs566190508	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151533207	GAAATAACACTTGAA[A/G]GAATCAGTTAATTTT	4703
rs566217786	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151658261	ACTGTGTTTGAAAAA[C/T]AATCTATAACAAACT	4703
rs566221198	snp	A/C	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151664382	AGGTGTCTTGTGTCA[A/C]ATGGGATGGCATTCC	4703
rs566222665	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151724491	GTTACTAGGAAAACA[C/T]TGACCATGCCAACAT	4703
rs566235446	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151607657	TGAAACATTAAGCCT[C/T]AGCTAATGTTTGGCT	4703
rs566239476	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151707247	CAATTCTGTTTCTGG[C/T]TTGGGGACAGATATA	4703
rs566249311	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151567837	AAAGAATTTGAACAA[C/T]TGCTTTTAAAAAAGC	4703
rs566260207	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151725053	AGAGCATTACCCCAA[C/T]GACTCTAGGTCTGCA	4703
rs566270715	snp	A/G	0.00159617	0.0282053	intron-variant	NEB, RIF1	GRCh38.p7	2:151527788	GGACCCTGTGGTCCC[A/G]AAATAGAGGCTAAAA	4703
rs566289994	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151614972	CTGTTTGACATTAAG[A/G]ATATTTTAGAATAGT	4703
rs566299587	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151641839	TTTATTATACTTTAA[C/G]TTCTAGGGTACATGT	4703
rs566341392	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151612011	ACAGAGAATTAGGGG[A/G]CAGGGTGTTGAGAAG	4703
rs566341488	snp	A/G	0.00159617	0.0282053	intron-variant	NEB, RIF1	GRCh38.p7	2:151489534	TTCCTCAGTAGCTGG[A/G]GCTATAGATGCACCA	4703
rs566362863	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151673010	TCTCTTGGTTTCATA[A/G]GGTTTCATAGGTTTC	4703
rs566364165	snp	A/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151626856	GCTCCCATATATTGT[A/T]ATCTAACAGAATAGA	4703
rs566381567	snp	C/T	1.91313e-05	0.00309278	missense	NEB	GRCh38.p7	2:151664835	TGAATGGTGGTCTTG[C/T]CCTTGTTCCATTTTT	4703
rs566388572	snp	A/G	6.6324e-05	0.00575826	missense	NEB	GRCh38.p7	2:151553905	TCCATTCGTGGAGGC[A/G]CAGGCGGTAATCAAT	4703
rs566397629	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151549966	ACAATGAGTGAAATG[A/G]TTTATTGAAAGTAGT	4703
rs566403951	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151714657	CCCAACAGATGGATC[A/T]GGGAGACATGATTCA	4703
rs566427472	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151561131	CAAGCAACAATAGGT[C/T]ATTCACCTCTGTTGT	4703
rs566464624	in-del	-/AA	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151713598	CTGAAATCTCATATT[-/AA]TTTTCTTTTGTGGAT	4703
rs566465441	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151502636	AGTTAAAATTTCACA[C/T]CAGAACTAAATACTA	4703
rs566474049	in-del	-/A			intron-variant	NEB	GRCh38.p7	2:151545576	GCAAAACTCCATCTC[-/A]AAAAAAAAAAGAAAA	4703
rs566476860	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151509900	GGCGCGAGCCACTGC[A/G]CCCGACCAAGAGTTT	4703
rs566505821	snp	A/T	0.00874735	0.0655527	intron-variant	NEB	GRCh38.p7	2:151655538	AACAAACTCAGATTT[A/T]AAAAAAAAATCTTTT	4703
rs566519174	in-del	-/ACTT	0.00557542	0.0525036	intron-variant	NEB	GRCh38.p7	2:151697709	CACGCTGATTATAAC[-/ACTT]ACATTTTCTAACACT	4703
rs566521476	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151518602	AGTTCAGTATTGTCC[A/G]TTAAGATGTAAACAC	4703
rs566522551	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151594435	TAAATTGGCTCAACA[C/T]TGGCAGTCATTACAT	4703
rs566527888	snp	A/C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151704737	GCACAGTGCGAGCAC[A/C/T]CACTGACCTGCGCCC	4703
rs566536629	snp	A/C	0.00199481	0.0315187	intron-variant	NEB, RIF1	GRCh38.p7	2:151509381	TCGTCCTTTTATTTT[A/C]TTTTTATTGTTTTTC	4703
rs566539789	snp	C/T	2.08644e-05	0.00322983	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151531090	CTTGTTGTATTCCAA[C/T]TTATAAAGGATCTGA	4703
rs566546892	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151720668	GAGATAGGAGATTAA[C/T]TGTCTTCTTGGAAAC	4703
rs566551082	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151693369	GATCATCCTGTCACC[C/T]AGGAATTAAGCCCAG	4703
rs566554370	in-del	-/CTT	0.0023933	0.0345097	intron-variant	NEB, RIF1	GRCh38.p7	2:151496066	TAGGAAAATCTGTTA[-/CTT]CTTGATATTAGAACT	4703
rs566604130	snp	C/T	3.31274e-05	0.00406972	missense	NEB	GRCh38.p7	2:151666182	ACTGTCTGTAGTTGG[C/T]GTTGGTGGCAACCTC	4703
rs566605570	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151539640	TGAGACACAAAACCC[A/G]TAAGGATTGGCTATT	4703
rs566608554	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151512100	CAGTGGCGTGATCTC[A/G]GCTCACTGCAAGCTC	4703
rs566646071	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151544063	TAGGCTGTCTCCCAA[C/T]CCTTCTAAATTCAGG	4703
rs566651804	in-del	-/AT	0.00199481	0.0315187	intron-variant	NEB, RIF1	GRCh38.p7	2:151489840	TCATTAATATGAAAC[-/AT]GTAATAAAAGAGCAT	4703
rs566670037	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151591865	AACATTGAGATGTAC[A/G]TTACACAGACACACG	4703
rs566673738	snp	C/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151496474	GAAAACACAGTCGTC[C/T]AAGGAGCCAGAAGTT	4703
rs566679460	snp	C/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151495800	CATAATTTATATCAT[C/T]ATTCTTGAAGGAGGG	4703
rs566694679	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151656720	GAGACCCAGAGAGCT[A/G]AGCAACCTGCTGAGG	4703
rs566701444	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151538761	CTTCTTCACTAAGCA[G/T]TCTTAAAACTTCATT	4703
rs566706198	snp	C/T	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151660441	AGTTTTAAATTTTAA[C/T]GAACATTAACAAATG	4703
rs566722585	snp	A/G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151610382	CTGTAACAACAAAGG[A/G/T]AATGGTCTTGAGAGG	4703
rs566740147	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151547335	AAGTGCTTATCAGAA[A/G]AGGCTGTTCAAAGAC	4703
rs566742054	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151661719	TTTGAAATGCTGCTA[C/T]AGGCATGTAATCTTG	4703
rs566775299	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151546818	CCCACCTCAGCCTCC[C/G]AAAGTGCTGGGATTA	4703
rs566784626	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151693917	CTTTGCCCTTACATT[A/G]ATTTCTTTACTTCTT	4703
rs566828890	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151581238	CTAGGTATTACTCTA[C/T]GTGTATCTATAAGTT	4703
rs566889654	snp	G/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151494638	TCAGCTGTTTGTTTT[G/T]TTTTGTTTTGTTTTG	4703
rs566890411	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151574341	AGCCAATACTTCCAG[A/C]AAATGTTAAATAATG	4703
rs566952319	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151708914	CTTCTTATCACCTGC[C/T]CTGCTACCCTCCTGG	4703
rs566973184	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151660011	TGTGCCACCAATATA[C/G]TCATTCAAGGAAGGA	4703
rs566977223	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151495652	TTGCAGTTAAAGACT[A/G]CAGTAAAACTAAAGA	4703
rs566989836	snp	A/G	8.49481e-05	0.00651666	synonymous-codon	NEB	GRCh38.p7	2:151688292	GGCTTTGGTACTTAC[A/G]TCACTCAGATTATAG	4703
rs567006996	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151731611	CTGGTCAGACACAGA[C/T]GCTGTAATGGGAACA	4703
rs567009676	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151655749	AATTAGATTTCTCCA[A/G]ACAAGAACCAGAGCC	4703
rs567012454	snp	A/G	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151730915	TTCTGCCTGTATGTC[A/G]TTACACATAGCAACA	4703
rs567012762	in-del	-/CAAAA			intron-variant	NEB	GRCh38.p7	2:151698095	CAAAACAAAACAAAA[-/CAAAA]AGAAAAAAACCTGAC	4703
rs567022787	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151733041	GACAATGTATTTTTC[A/G]AATGATTAATTCACC	4703
rs567026785	snp	C/T	0.00119737	0.0244387	intron-variant	NEB, RIF1	GRCh38.p7	2:151529675	ACCTGGGACCACAGG[C/T]ATGCGCCACCTCACC	4703
rs567045621	snp	C/T	1.67273e-05	0.00289195	missense, intron-variant	NEB	GRCh38.p7	2:151654030	CTTTAGCTAGCTGTA[C/T]AGAAATTGCATCAAC	4703
rs567047486	in-del	-/C	0.00318978	0.0398085	intron-variant	NEB	GRCh38.p7	2:151677407	AAGAAAATGTTAGTG[-/C]CCAAACTACACATAA	4703
rs567049545	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151573923	TCTGCAAATAATGAT[A/C]ATTTGGCCTCTTTCT	4703
rs567069085	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151516372	GCTACCACTTTTGGA[C/T]GACAGGAAACTGGCC	4703
rs567088469	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151681075	GGAACCAGACAGACT[C/T]CTTTCTTAATTTCTT	4703
rs567096026	snp	C/G	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151653792	TAGAGGTCGTCTGGC[C/G]CGACCTCTATTCAGG	4703
rs567102938	snp	A/C	8.28096e-05	0.00643412	missense, intron-variant	NEB	GRCh38.p7	2:151639997	TGCATTTTTCCACAT[A/C]CAAAGAGCCAATGGA	4703
rs567111784	snp	A/G	6.23111e-05	0.00558137	intron-variant	NEB	GRCh38.p7	2:151560544	TGGAGTGGAGAGCAG[A/G]GGAGGGGAGGGAGGG	4703
rs567125126	in-del	-/GGGTAGTAACAAGAATG	0.0225045	0.103662	intron-variant	NEB, RIF1	GRCh38.p7	2:151486662	TACAGATCTATTATT[-/GGGTAGTAACAAGAATG]GGGTAGTAACAAGAA	4703
rs567135338	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151680622	AGATGCTTGTGTAAT[C/T]GGGTCTCTTCATATT	4703
rs567143080	snp	A/G	0.000798403	0.0199641	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151503180	TGTTCAAGTATAATC[A/G]GAAATGTGAGTCATT	4703
rs567146339	snp	G/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151509341	GAAAACAGTTCTCAT[G/T]GTCCTGGGAAAAGAA	4703
rs567168669	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151516262	AAGACATATGGTAAA[C/T]ATTTACTACCTAGAG	4703
rs567208277	snp	C/T			intron-variant, utr-variant-3-prime, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151498033	GTGTTGTTATCCACA[C/T]AAATGGAAACATTCA	4703
rs567213467	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151639754	ATAGACAGATAGATA[A/G]ATGCCTTTTATTACT	4703
rs567250105	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151646810	ATGTGCCACCATACC[C/T]GGCTAATTTTTGTAT	4703
rs567255080	snp	A/G	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151502561	AGGAATGGAGGAAGA[A/G]AACAGAGTATTACAG	4703
rs567259977	snp	A/G	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151508661	AGGCATTTCCAGAAT[A/G]TGGCTCTTGATGCTG	4703
rs567277006	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151723609	AGAGCAAAGGTAAAT[A/G]AAATTCACAGATAAC	4703
rs567282220	snp	A/G	0.00118119	0.0242735	intron-variant	NEB	GRCh38.p7	2:151563812	TTAGGAGAGGAAAAG[A/G]TCATACTGACCTCAC	4703
rs567310102	in-del	-/TTAT			intron-variant	NEB, RIF1	GRCh38.p7	2:151495824	GGAGGGGATCAGGGA[-/TTAT]TTATTTTTCCCAAGG	4703
rs567311565	snp	C/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151515543	AAAATCACTGAATAG[C/T]TTAGGTGGGCAGTGA	4703
rs567312873	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151673845	TTCACGCCATTCTCG[G/T]GCCTCAGCCTCCCTA	4703
rs567324487	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151523862	CCTACTTCCTAGCCC[A/G]GGCAGTTAATATATG	4703
rs567332802	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151680553	GCACAATATACATTA[C/T]TGTAAATATATGAAT	4703
rs567345432	snp	A/T	0.030665	0.119967	intron-variant	NEB	GRCh38.p7	2:151699133	TTTTTTGTTCTTGCG[A/T]TAGTTTACTGAGAAT	4703
rs567345506	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151708783	AAAAAAATTACCAAC[C/T]TCTTCCATAGTCTTC	4703
rs567365256	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151559788	CACACTGGGTCCTCT[C/T]AGGGAGTAGGGGGCT	4703
rs567369388	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151673066	AATATGAGTACCAGC[C/T]ATAGGATAGCTGGGC	4703
rs567372148	in-del	-/ATTGAC			intron-variant, cds-indel, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151498095	CAGATGAAGTAAAAA[-/ATTGAC]ATTAACTGTATTATA	4703
rs567375307	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151680960	GCAAAAACACTAGAT[A/T]CTTGATTGGCTTGAT	4703
rs567386118	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151657445	CACCTGCTTTTTTGC[C/T]GGCCAGCGCAGGGAA	4703
rs567389268	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151566294	ATCCCCTGGGTCCCA[A/G]CCAAACCTATTCTTG	4703
rs567412477	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151568006	ATCTCTGCCTTTGGC[A/G]TAACTGGAATCCCTG	4703
rs567416438	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151625988	GTAGTATGACTATAT[C/T]AACAAATCCTTCCCA	4703
rs567445698	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151550874	TGGTCTTGAACTCCA[A/G]GCTCAAGCCATCTGC	4703
rs567455283	snp	A/G	0.029116	0.117091	intron-variant	NEB	GRCh38.p7	2:151703373	GAGTATCTTTGTGGC[A/G]TTCTCTGTATTTCCT	4703
rs567468763	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151610679	GAGGAAGGTAATAGG[C/T]CAATTCCAGAAAGGA	4703
rs567478677	snp	A/G	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151572599	CACCCAAGCTGGAGT[A/G]AAGTGGCACGATCTC	4703
rs567486086	snp	A/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151573470	CCCCTTGATTCAGCC[A/T]CTTGACAAGAATGCG	4703
rs567492697	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151704592	AGCCGGTCAGAAAAG[C/T]GCAATATTCGGGAGG	4703
rs567495727	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151718244	AACATGATGAGTAGG[A/G]TTAAGAAGGACACAG	4703
rs567501862	snp	C/T	9.94992e-05	0.00705264	missense	NEB	GRCh38.p7	2:151666140	CCACATTCAAGGCAT[C/T]GGGCAGGAGAGTGTA	4703
rs567517023	snp	G/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151546735	GGCTAATTTTTGTAT[G/T]TTTAGTAGAGACAGG	4703
rs567524588	snp	C/G	0.000399281	0.0141238	missense, intron-variant	NEB	GRCh38.p7	2:151579587	CAGTTTAGGGTCTTC[C/G]TTGGCGCTGCGACAG	4703
rs567526465	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151667184	TCCATGGATTTTTTT[C/T]CTTCATGGAAATTAT	4703
rs567531004	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151683205	AATTGTATAAGACTT[A/T]ATAGAACTATTCGTA	4703
rs567547678	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151674423	ATTTAAACAAGCATT[C/T]GATTACTTTTCAAAA	4703
rs567552070	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151659330	GAGACAGAGTCTTGC[A/G]CTGTCACCCAGGCTG	4703
rs567553899	snp	A/C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151626261	CTAAGACTAGAGGTG[A/C/T]GTGTCACCACACCCG	4703
rs567580290	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151702484	TAAAGTCTCCCATTA[C/T]TAATGTGTGGGAGTC	4703
rs567589481	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151553251	CGCCTTCCTGAGAGA[C/T]GGTTGCTCTGCTCCT	4703
rs567607576	snp	C/T	0.000297059	0.0121836	intron-variant	NEB, RIF1	GRCh38.p7	2:151494139	GCAAAATTAAAAGCA[C/T]TTTTGTTTCTCAAGA	4703
rs567612671	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151656979	AATAGCTTTATATTC[A/G]TGGAGCTCCTTTTCC	4703
rs567646712	snp	A/G	5.39108e-05	0.00519158	intron-variant	NEB, RIF1	GRCh38.p7	2:151493903	CCCGAAAGTCACTAC[A/G]AGGTAATAATCACTA	4703
rs567659738	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151579032	GTTGCAGTGGGCTGA[A/G]ATTGCACCACTGCAC	4703
rs567668342	snp	C/T	0.00517822	0.0506191	intron-variant	NEB	GRCh38.p7	2:151726023	GATCTGAATTATATT[C/T]TGTAAATTTAGGAAT	4703
rs567668986	in-del	-/GGAA	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151578677	CAAGGAGGGAAGGAG[-/GGAA]GGAAGGAAGGAAGGA	4703
rs567694727	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151705290	ATATGCAGCTGATAA[A/G]GCAGATTATTGTCAC	4703
rs567700506	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151543923	GTCAAGAATCTATAC[A/C]ATTGAAAACTCAAAA	4703
rs567743283	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151706097	TAAAAGAAAGCAAAC[A/G]TGCTTTACAGTGATT	4703
rs567755362	in-del	-/A	0.267908	0.249358	intron-variant	NEB, RIF1	GRCh38.p7	2:151488479	TAGTGAGCCTCTACC[-/A]AAAAAAAAAAAAAAA	4703
rs567768015	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151572710	CACCACTATGCCTGG[C/T]TATTTTTTGTATTTT	4703
rs567792020	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151693882	TGCTTTTGAGTTTAT[A/G]CCTTATGTAGTTTTT	4703
rs567792534	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151500007	TCAAATAGATACAAA[C/T]AATAATATACTTACT	4703
rs567794299	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151507742	AGGGGTTTTCGCCAT[A/G]AACCTTGCCATGGGT	4703
rs567797595	snp	A/G	0.00716266	0.059414	intron-variant	NEB	GRCh38.p7	2:151715941	CTTTTAAGAATCCCC[A/G]CTGCATATTTAAATA	4703
rs567799866	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151666839	AGTGCTAGGATTAGA[C/T]GTGTGAGCCACCATG	4703
rs567810005	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151646036	TAATTAATTAAAATA[A/G]TTCAGGGATTCAGAG	4703
rs567845113	snp	A/G	0.00279162	0.0372561	intron-variant	NEB, RIF1	GRCh38.p7	2:151487664	TATAATGAGCATCCT[A/G]CCGTTTATCTTTGGG	4703
rs567862993	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151705982	TAGTGTACACTGTAG[A/G]TGATGGGTGCACCAA	4703
rs567874589	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151544593	TTCTAGTCTGAGTGC[A/G]AGTGCGGGCTGAAAT	4703
rs567875243	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151687137	AAAATATCTAGTGAT[A/G]TTTTCCAAAAGGTTT	4703
rs567882559	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151569911	TTGATATAAAGTCCA[C/G]GTCCTTCTTGGATTT	4703
rs567919770	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151577157	TTCAGAATTCAAATC[C/T]GATGTCACAACATTC	4703
rs567934849	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151604277	TTATGAAATATGTAT[A/G]TGATTATGCAAAGGT	4703
rs567949095	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151659974	ACAAGCAATGTCATG[A/T]TCCTTGTGGTGGACA	4703
rs567964368	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151696815	CCAAGCAAATAGAAC[C/T]TCATGCCCCACAAAG	4703
rs567985801	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151653523	TTTTTATGTCCCAAG[G/T]TAATTTATTACAATT	4703
rs567999585	snp	A/G	1.65971e-05	0.00288067	missense	NEB	GRCh38.p7	2:151663648	TAGTTGGCATTGGTG[A/G]CCACTTCCTGAGACT	4703
rs568043024	snp	G/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151504645	AATCCCAAGACCAAG[G/T]TCCTCCCCTTTTATT	4703
rs568077695	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151648450	GTTTCTCTTTAAAAA[A/T]TTTTTTTATTTCCAT	4703
rs568081136	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151663295	TCTTTCTGAAATGAA[A/G]TTCCATTTGCTGTTG	4703
rs568101617	snp	A/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151712234	GGCAATTGGGCCTGA[A/T]CCCCAAAACTGAGAT	4703
rs568110378	snp	A/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151517194	TGTTGTATAAATAAA[A/T]TTTTCTCATCCTCAT	4703
rs568110476	snp	A/C	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151525622	TACTGAGGCCCAAAG[A/C]GGTAGTTTTACCTTT	4703
rs568113302	snp	A/C/T	1.965e-05	0.00313443	intron-variant	NEB	GRCh38.p7	2:151547742	CCGATACAGTCTCTA[A/C/T]GTTGGAGGAAATATC	4703
rs568134439	in-del	-/T	0.49753	0.0350569	intron-variant	NEB	GRCh38.p7	2:151563012	TTGAAATTTCCCATC[-/T]TTTTTTTTTTTTTTT	4703
rs568135973	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151649861	TTTCCCCCTCATATA[C/T]TCTACCCCAACAAAA	4703
rs568146843	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151524966	CCACCACGCCCAGCC[A/G]AGATATGCTATCTTT	4703
rs568150421	snp	C/T	0.000105513	0.0072626	intron-variant	NEB	GRCh38.p7	2:151690622	TGAAAAATAATAATA[C/T]TGGGATGGTAGATGA	4703
rs568197703	snp	A/G	1.89593e-05	0.00307885	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151642813	TAAAACTTCAGGGGT[A/G]TCTGGCATAATGTGG	4703
rs568203312	snp	C/T	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151649757	ATCCATTTATCCTGA[C/T]TCAGCTAAACTAAAA	4703
rs568248456	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151558951	CATTGGAATCTAATT[A/G]AACTAAAGAACTTCT	4703
rs568248647	snp	A/G	0.000911297	0.0213265	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151529210	GTTTCTGGAACTTAC[A/G]TTGGTGTTGACTTTG	4703
rs568270970	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151691081	TGCTGAAGCCTTACA[C/T]AGTGACTCTTTAGTC	4703
rs568294159	snp	C/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151526628	GAAAACAAATCATGG[C/T]GTTTCCATAAAGAGT	4703
rs568317333	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151717916	TGGAATGCAGTAGCG[C/T]GATCTCGGCTCACTG	4703
rs568323762	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151620665	AGCTCAGCATACACA[C/T]ATCTAGCTTTAATCG	4703
rs568335746	snp	C/T	2.06345e-05	0.00321198	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151526241	TTCCTCTTTCCTTGA[C/T]ATGTTTCTCTTTGTA	4703
rs568352529	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151695325	AAGCATACATGAGAC[A/G]TAGCATTCTGAGGGC	4703
rs568355799	snp	C/G	1.66532e-05	0.00288554	intron-variant	NEB	GRCh38.p7	2:151540680	CCCAGTGCCTCAGTG[C/G]TGAATTCCCATCTTA	4703
rs568362014	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151641285	ATTATATAAGCATTT[A/C]TATGTGTCATTAAAT	4703
rs568371034	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151517898	GGTATATGACTGTAT[C/T]TTAAAAATTTAGTAA	4703
rs568389927	snp	C/G/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151487134	CCTTTTTCTACCTTT[C/G/T]GAAGAGGTCAGTCTT	4703
rs568392776	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151650046	TCAAATAAAATGATC[C/T]AATATAAAATTTTAT	4703
rs568409508	snp	A/C	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151491560	GGTATTTTTATGCCA[A/C]ATGGGCAGCTCAGAA	4703
rs568412898	snp	C/T	0.00279162	0.0372561	intron-variant	NEB	GRCh38.p7	2:151666610	TTAAAAATGGAATAA[C/T]GGAATAGTTTATATT	4703
rs568415782	snp	C/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151683413	TGTTGTCTGACCATA[C/G]GTGGTACCAAAAATT	4703
rs568415904	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151675177	TATGTTCCAGTAGGG[A/G]ATTTGTGAGAAATGG	4703
rs568429436	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151688453	TTGAATTTATTTAGG[G/T]CAGCATATATAGCTA	4703
rs568451191	in-del	-/G/GG	0.00322355	0.0400198	intron-variant	NEB	GRCh38.p7	2:151546308	GGCATCCAGCTGTGC[-/G/GG]GGGGGGTAATTATGC	4703
rs568465937	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151619030	GTAAGAATGATAGAA[G/T]TTTCCCATCAGTAAG	4703
rs568470719	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151575172	AAGGGGACCCTGACA[C/T]TTGAAAGTAGGAAGA	4703
rs568470795	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151593646	TCCATCCTGCCCCCC[A/G]TCTCTCTCTCTTTCT	4703
rs568473495	snp	A/T	1.67511e-05	0.00289401	missense	NEB	GRCh38.p7	2:151537928	CTGGACGATCAGGAA[A/T]GGACCTCCAGATACC	4703
rs568527189	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151704731	GCTCACGCACAGTGC[A/G]AGCACTCACTGACCT	4703
rs568531004	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151712070	AAGAAACTGAGAAAG[C/T]TATAAAATGCTCACA	4703
rs568531186	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151540512	TTTCCAACCAAGCCA[C/T]CTACAGGTCTTGTGG	4703
rs568557026	snp	C/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151507944	CTGGGATATCCAGAG[C/G]CATCTTCCTCAGCAC	4703
rs568565482	in-del	-/TG	0.00318978	0.0398085	intron-variant	NEB, RIF1	GRCh38.p7	2:151487045	ATGTATGCATGAAAT[-/TG]TGTGTGTGTGTGCGC	4703
rs568580858	snp	A/C	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151510780	AATTTCAGGCATCCA[A/C]TAGAGGTCTTGGAAC	4703
rs568599013	snp	A/C	0.000580109	0.0170211	synonymous-codon	NEB	GRCh38.p7	2:151562209	CAGGTCATCTTTATA[A/C]ACATTCTGCAAGAAA	4703
rs568605073	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151719322	AGGAGAATTATCTTT[C/G]TAATCTTCCGTGACA	4703
rs568608277	snp	A/G	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151591513	AGCTACTGAGTCAGC[A/G]TTACTGATGTATTTA	4703
rs568620891	snp	A/G	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151511394	TTACAATATACAACT[A/G]TATGTTTCCAGTAAA	4703
rs568626228	snp	A/G	0.000399281	0.0141238	missense	NEB	GRCh38.p7	2:151554007	TCTTGTTCTTTTCAT[A/G]AACTGATCTGTACAG	4703
rs568626255	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151561694	CCTCACTTTTAACAT[A/T]CCATTACAACTGCCC	4703
rs568634365	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151726696	TGATTCTCAACCTGG[C/G]TACACATTAGAATCA	4703
rs568636683	in-del	-/TT	0.00199481	0.0315187	intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151497282	GAGTTATCCATGTTA[-/TT]TTTTTTTTTCCTTTT	4703
rs568655110	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151719295	ACTGAGGCCATGGGG[A/G]AATGTCTCAAGAGGA	4703
rs568658040	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151567867	CCAAGGGGGGTGGTG[C/G]GCGGGTGAAGAAACA	4703
rs568688863	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151568545	ATGATTGCATTCTGA[A/G]TGTAAGTAGATGGAA	4703
rs568697998	in-del	-/A	0.137527	0.223271	intron-variant	NEB	GRCh38.p7	2:151720138	GATTTTTAAAAAAGT[-/A]AAAAAAAAAAAGTTC	4703
rs568712971	snp	A/G			intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151533936	CTCAATCTGCAGTTT[A/G]CAGTTGCAGTTTTCA	4703
rs568714726	snp	A/G	0.000101291	0.00711586	intron-variant	NEB	GRCh38.p7	2:151603785	GTTCTACATGAAGGA[A/G]AGGAACACAGAGTGG	4703
rs568741653	in-del	-/T	0.400147	0.19989	intron-variant	NEB	GRCh38.p7	2:151546557	TTTTGGTTCATCTAC[-/T]TTTTTTTTTTTTTTT	4703
rs568751958	in-del	-/C	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151542290	GATTGGCCCCTTTCA[-/C]CCAGTACATTCTCCC	4703
rs568762355	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151733243	CCCAGCACAGAAATT[A/T]TCTTATGACATTATA	4703
rs568799016	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151733873	CTAAGCTTCTAATGC[A/G]GAAAACAGCGAAAGG	4703
rs568814745	snp	C/T	0.000364407	0.0134934	missense, intron-variant	NEB	GRCh38.p7	2:151627548	AGGTCATAGGCCTGC[C/T]GAGCATGGATGACAT	4703
rs568830640	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151675114	CCTTTAAAATTGTCC[C/T]ACATTTGAAAAGGCC	4703
rs568835715	in-del	-/A			intron-variant	NEB, RIF1	GRCh38.p7	2:151509829	GGTCAGGATGGTCTC[-/A]AATCTCCTGACCTCA	4703
rs568850342	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151555996	TTTGCCAAGAATCTT[C/G]CCTCTATAATTTTGT	4703
rs568850372	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151594546	GGTATGGTGAACAAG[A/G]GTAATGAAAACAATA	4703
rs568854960	snp	A/G	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151704794	AACCCGGTACCTCAG[A/G]TGGAAATGCAGAAAT	4703
rs568869829	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151668683	GGATGTTTTAATAAA[C/T]AATTAAAAGTTGTAA	4703
rs568889862	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151618997	TTGATAAGTATTAGA[C/T]GACTGGTTTCGAAAA	4703
rs568910689	snp	C/G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151653793	AGAGGTCGTCTGGCC[C/G/T]GACCTCTATTCAGGA	4703
rs568918412	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151649394	ATGTAAAGTGTATAG[A/C]ATATTACATATAGTA	4703
rs568941097	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151529702	CACCCGGCTAATTTT[A/G]TATTTTAGTAGAGAT	4703
rs568950144	in-del	-/TTATTA	0.0138799	0.0821421	intron-variant	NEB	GRCh38.p7	2:151634726	GCAACCGAGGAGAAT[-/TTATTA]TTATTATTATTATTT	4703
rs568970805	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151685855	TTAGAGACGGTGACC[C/T]AAGCTGGCAAGTACA	4703
rs568978130	snp	G/T	0.0130921	0.0798413	intron-variant	NEB	GRCh38.p7	2:151536833	ACTTTATATTGGCTG[G/T]CATATCAGCTTTAAT	4703
rs568996390	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151660511	ATATTGCATGTAACA[C/T]AGCTATTTAATATTT	4703
rs569013971	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151705218	TTACTACTAACTCTT[C/T]TTCTCTGCCAGGATT	4703
rs569014816	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151535924	ATTCGTTTGTTTGTT[C/T]TGAGACAGGGTTTCA	4703
rs569058869	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151538996	TTTTTTAGATGGATC[A/G]TAAGATTGCTTAGAT	4703
rs569100746	snp	A/C	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151525872	GAAGCTACATAAAGG[A/C]AGCAAAAGGCAACTG	4703
rs569102821	snp	C/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151531651	GAGGAGAATCCTGTG[C/G]ATAACAGGACATCTC	4703
rs569104377	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151682137	GAAGCCAGATACAAA[A/G]TAAATTTCTAGAAAA	4703
rs569107587	snp	C/T	1.67562e-05	0.00289444	intron-variant	NEB, RIF1	GRCh38.p7	2:151490099	AAAAGGGGGCAAATT[C/T]TTTATAAGAAGAAAA	4703
rs569117771	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151490729	GACCAAAGGTCATGG[A/G]ACAGTTAAGTTGTAC	4703
rs569139721	snp	A/G	3.10005e-05	0.00393692	intron-variant	NEB, RIF1	GRCh38.p7	2:151531137	AAGACATCATGTCAT[A/G]CTTCTCAATGTATAA	4703
rs569156383	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151648592	TACCTGCTAACCACT[C/G]ATATTGTGTATGGAT	4703
rs569156711	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151543673	GTATTGATTTTTAGA[A/G]ACGGGGTCTCACTAT	4703
rs569159953	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151663249	ATTATGCTTTTGACC[A/G]TCTTTGCTAGACATA	4703
rs569192098	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151646851	AACAGGGTTTCGCTA[C/T]GTTGTGCAGGCTGGC	4703
rs569212511	in-del	-/CATTA			intron-variant	NEB	GRCh38.p7	2:151720537	TTGTATGTTCTCTTT[-/CATTA]CATCTTCTACTGTAA	4703
rs569214142	in-del	-/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151515867	AATTTTTCTTTATAG[-/T]TGGAGGAAGAGAGGC	4703
rs569227724	snp	C/T	0.00119737	0.0244387	intron-variant	NEB, RIF1	GRCh38.p7	2:151523991	GTATGAATCAGACCC[C/T]GAGGATGAAACTCTT	4703
rs569229209	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151694029	TATACTTATGTATAT[G/T]AAGCTCGTTTCTAGG	4703
rs569237119	snp	A/G	0.00119737	0.0244387	intron-variant	NEB, RIF1	GRCh38.p7	2:151488579	TGAGTCCATGAAGTC[A/G]AGACTGCAGCGAGCT	4703
rs569248375	snp	A/G	9.84979e-05	0.00701707	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151591390	GGCATGCTGGATCCC[A/G]ATGGCATCTGCTCGC	4703
rs569276450	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151583173	TATGAAATATGTATA[C/T]GACTATGCAAAGGTA	4703
rs569300032	snp	C/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151495046	AAGCAAAGGGTTTCC[C/G]CTACCCTCTTTTTCT	4703
rs569301301	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151527684	ATTTCAAAACATCTC[A/G]AATCATGATTCCTAA	4703
rs569340100	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151527334	GTTCTGAGCTCGCCT[A/G]TCGCTCCCCCAACCA	4703
rs569357091	snp	C/T	2.85874e-05	0.00378059	intron-variant	NEB	GRCh38.p7	2:151654149	TCTATATAAAGAATA[C/T]CAATAGATTATTAGG	4703
rs569358371	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151725822	AAAATGATTCTTTCA[A/G]TCTTTTTTTTTGTCT	4703
rs569359041	in-del	-/T	0.00159617	0.0282053	intron-variant	NEB, RIF1	GRCh38.p7	2:151518252	AGGGAATCTATGAAA[-/T]TTTTTTTTCACATTG	4703
rs569378468	snp	A/G	0.00119737	0.0244387	intron-variant	NEB, RIF1	GRCh38.p7	2:151533126	TACTTACTATCTTCA[A/G]TCTCTAAGGAATCTA	4703
rs569398871	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151657850	AAACACAAAAGCAAG[A/G]TTAAGAAGCATTCAC	4703
rs569401630	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151524828	GTGCACCACCATGCC[C/T]GGCTGATTTTTGTGT	4703
rs569420905	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151617268	ATGGTAGTTTGTAGT[A/C]TGTGTAGTAAATTAG	4703
rs569421854	snp	A/G	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151532253	TATACACATGTACTC[A/G]GAGGCCCCCAGAGGT	4703
rs569450156	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151567870	AGGGGGGTGGTGGGC[A/G]GGTGAAGAAACAAGA	4703
rs569486464	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151575020	ACTGGGATTATAGGC[A/G]TGAGCCACCATGCCC	4703
rs569523954	snp	A/C	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151486084	AGTAAAAGGAACCCA[A/C]AAAATAGGAAATACT	4703
rs569538452	snp	C/T	8.73828e-05	0.00660937	intron-variant	NEB	GRCh38.p7	2:151640707	CATCTGTTTTAACTT[C/T]TAGTAAAAAGCAATC	4703
rs569538550	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151631897	GATTCTTATTCCCTG[C/G]GATGTATTCTTCTAT	4703
rs569542176	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151691312	CCTGACTGGTCATGC[C/T]TGTTTTAGACCTTCC	4703
rs569542268	snp	G/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151520441	ACATAAAAATAAGTT[G/T]AGGTAGGCAGAGGGC	4703
rs569568388	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151540882	TTCATTCATTTCTAA[A/C]CATTCAGTGGGAAGG	4703
rs569573558	snp	A/C	1.65899e-05	0.00288005	intron-variant	NEB	GRCh38.p7	2:151640072	TATTCTGTTGACACA[A/C]ATAGCCAATAAATAT	4703
rs569580109	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151685559	TTAAAAGAAGCTTCA[A/G]ATTGCAGCAGTTAAA	4703
rs569603594	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151697787	AACTGACAATTGAGG[A/C]CAGGTGCGGCGGCTC	4703
rs569621146	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151678607	TTTTAGTAGTAGTGG[C/T]AGGATGTTAATATCA	4703
rs569670606	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151577782	CAGGGTTTCACCATG[C/T]TGGTCAGGCTGATCT	4703
rs569675501	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151651024	GAACTCCCAGGCCTA[A/C]TTTTCTAGCTTCAGC	4703
rs569677481	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151530964	AGGAGGCCAAGATGA[A/G]AGGGACTGCTAAACC	4703
rs569703584	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151629011	TTTTCTTGTTTTCCT[C/T]GTCTTTGTCTTTCTG	4703
rs569729941	snp	A/G	0.00159617	0.0282053	intron-variant	NEB, RIF1	GRCh38.p7	2:151514487	GATTGATTCTCTCAG[A/G]CAAAGAAGAAAATAA	4703
rs569734890	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151541642	TTTTACATAGAAAAG[A/G]CAGGAGCCCTCCCAC	4703
rs569742329	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151636053	GTAGGTTACAGATCC[C/T]TCTTATAAACATCAA	4703
rs569781774	snp	A/C	1.72841e-05	0.00293969	intron-variant	NEB, RIF1	GRCh38.p7	2:151492363	GACAGGCAGCCAGCC[A/C]ATCCTAAAGAATTCC	4703
rs569794468	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151501851	AGAGAGAGAGACAGG[C/T]AGGTTTGGGGGAACA	4703
rs569805031	snp	C/G	0.00488653	0.0491873	intron-variant	NEB	GRCh38.p7	2:151606760	GAATGGAAAAATAAG[C/G]AAATTTACTCAAATT	4703
rs569807131	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151513241	AGAACTCCCAAGATA[C/T]TCTAAGCAAGGAATT	4703
rs569844485	snp	A/G	0.125182	0.216612	intron-variant	NEB	GRCh38.p7	2:151722473	GAAGTATCTTCTGAT[A/G]GCAAGAGCTCTTTGT	4703
rs569846162	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	NEB	GRCh38.p7	2:151734497	ATGCCTGGGCTCCGA[A/C]TTATCATGTGGCAAG	4703
rs569849433	snp	A/G	2.89197e-05	0.0038025	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151513687	CCAGGTCTCGCTTAT[A/G]TTCTTTCTATAGTAG	4703
rs569860726	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151507125	TTTAAAAAAAAGTCT[A/G]TGCACAATAATTATG	4703
rs569875492	snp	A/G	0.00119737	0.0244387	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151498817	AAAAGAAGTCAGAGT[A/G]TTTAATTTTTAGTTT	4703
rs569888682	snp	C/G	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151553570	TTAACACTAAAAACA[C/G]AGGTACATTCTAGAC	4703
rs569893371	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151630550	CTTCAGTTTGCCAGT[A/G]GAATCCCATAAAATG	4703
rs569902276	snp	C/T			missense	NEB	GRCh38.p7	2:151677641	GTAAATTTGAGGGTG[C/T]CTGGATGTTGCCTGT	4703
rs569930213	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151564575	ACACATGTACACTAT[C/T]GGTCTCCTTTAAATT	4703
rs569934070	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151644394	TAGATTTTGTTCAAT[G/T]TAAAATTAAATTGAG	4703
rs569936628	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151498037	TGTTATCCACACAAA[C/T]GGAAACATTCATTAT	4703
rs569938511	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151506026	ATGACTCTAGCCACT[A/G]TGTGGTGGTGGTACA	4703
rs569960990	snp	C/G	0.00557542	0.0525036	intron-variant	NEB	GRCh38.p7	2:151571610	ATGTTAGATCTTCCG[C/G]TGAAGCATGATTGGA	4703
rs569962317	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	NEB	GRCh38.p7	2:151736323	TTCTAGAAATAGAAA[A/T]ACTGAGGCAGAAGAT	4703
rs569963280	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151508598	GAGCAGGTGCGGTCA[A/G]GGCTCCCAGCTATAG	4703
rs569966533	snp	C/T	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151636924	AAACAATAAATCCAG[C/T]TTAAAAATTACAGGA	4703
rs569999031	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151729222	TGTCCTACAAGTTAT[A/T]ACTCCACACAGTAAA	4703
rs570007021	snp	G/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151518867	TTGTAATAAATCTAG[G/T]GTATCAGTAGCAGAG	4703
rs570017063	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151641968	TCCCTCCTCCCTCCC[C/T]CCATCCTATGACAGG	4703
rs570049431	snp	C/T	1.65789e-05	0.0028791	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151519711	AGAGCTGGCTGTCTT[C/T]TGGATTGTATTTTGG	4703
rs570122863	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151569864	TTTAATCTGATACAA[C/T]TAAGACCTGTATTCA	4703
rs570130830	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151683663	CAGTATGGTGGTTCC[C/T]CTACAAATAAAAAAT	4703
rs570134110	snp	A/C/G	0.00016244	0.00901102	missense	NEB	GRCh38.p7	2:151690773	TGCAACAGTACAGGA[A/C/G]AATCAGTGACTGCCG	4703
rs570138741	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151675883	TATACATGAATCTAG[C/T]ATACTCAAAAGGCTC	4703
rs570142622	snp	C/T	4.98037e-05	0.00498993	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151612282	AGGCTGGCGATACTT[C/T]CTGTCACTCAGGATT	4703
rs570161989	snp	C/T	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151562424	AACCAATTAAATATT[C/T]AACATATGTGTCCTA	4703
rs570168676	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151726876	ATGAAAAAATAATTA[C/G]GAGATCCTACAATTT	4703
rs570173271	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151613960	TGTGAGAACAGACTA[A/G]TACAGAGTTGTTGCT	4703
rs570201668	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151541100	TTCTGATAGACCCCT[C/G]AACATATTTTCCCCT	4703
rs570203943	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151621158	AATCAGAAAAAGAAC[C/T]CTTTCTTTTACTTTC	4703
rs570218590	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151540222	CTCTTTAAAAAAATG[C/T]GTGTTTTTTTCCTAG	4703
rs570230631	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151670199	TTAACCCTTAGACAT[A/C]TGTGATAATGTGGGG	4703
rs570238837	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151548994	ACTTACTGGGATGGC[C/T]ACGATTTCCCTAAGC	4703
rs570243269	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151605952	GGATTACAGGCTCCC[A/G]CCACCACGCCCAGCT	4703
rs570245458	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151713935	ATCTGAACTGGGAGC[C/T]GTAAGAAAAGGGTGT	4703
rs570287825	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151616341	AAATGTGGGGAAAAA[A/G]TCAACATTTGGTTGG	4703
rs570322006	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151721512	CCTTGGGACCACCAC[A/C]TCCACATGGCCTTCT	4703
rs570324527	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151577280	CTATTCTTCCAGCCT[C/T]GTGTCATCTGTACTT	4703
rs570337448	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151670898	GCCCTTTCTCTCATA[C/T]CTATGAAAGCAGTTT	4703
rs570352251	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151612856	TTTTGGGGATAAAAA[C/T]GACGTCTTTTTCGTA	4703
rs570365650	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151605778	TGGGGGCAGGGTGCA[C/T]CTGGTAGCATAATTA	4703
rs570384266	snp	A/C	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151556593	CAGACTTTAAACCAA[A/C]AAAGATCAAAAGAGA	4703
rs570385120	snp	C/T	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151657644	TTAGAAAATCAGATC[C/T]GAAGAAGCAGGAGGC	4703
rs570401836	snp	A/G	0.000399281	0.0141238	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151606654	CTTGATTTCAATGGC[A/G]TCTGCCCTTATGTCA	4703
rs570407654	snp	A/C	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151706614	GCTCATAAGCAACAC[A/C]TCCATATGGAGGCCC	4703
rs570447892	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151569988	TGGTGATATGAAGTC[A/G]TAAAATGATGACAGA	4703
rs570473589	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151507588	TTATTACCATTGGAT[C/T]ATACCCCTCTTTGTC	4703
rs570511034	snp	A/G	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151518716	TCCTTAGAGAAAAGG[A/G]AATGGTTAATTGGAG	4703
rs570533384	snp	A/G	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151548897	CTTTCTGGCCACTAG[A/G]TTTGATTCCCAGGAA	4703
rs570546212	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151629814	TACCAAAAATACTAT[A/G]TAGCGTTAGAAATAA	4703
rs570598088	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	NEB	GRCh38.p7	2:151736253	CAAAACACACAGTAA[A/G]CATCCCTGTACATTA	4703
rs570638656	snp	C/G			missense	NEB	GRCh38.p7	2:151655840	TGGTATGTGCATTCT[C/G]CTTGGCAAGCACCAT	4703
rs570643172	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151649355	TGGGCTTATATATTA[C/T]ATAAAACTTCTGATA	4703
rs570682789	snp	A/T	0.000186369	0.00965141	intron-variant	NEB	GRCh38.p7	2:151619809	AGCACAAAGGGCTAT[A/T]CCCTGTTGTTCTTTC	4703
rs570690843	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB	NEB	GRCh38.p7	2:151735453	TGTCCTTACACACAG[C/T]GACAGAAATCACAGG	4703
rs570708987	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151734066	GCAAATGAAGCCCAG[G/T]AGAACAGGATAAATA	4703
rs570756591	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151670153	TACAAAAGAAAAAGA[A/C]TTGACACCAGTTATT	4703
rs570758069	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151577687	AGGTTCAAACGATTC[C/T]CCTGCCTCAGCCTCC	4703
rs570763682	snp	A/G	0.000154919	0.00879973	missense, intron-variant	NEB	GRCh38.p7	2:151642869	CTTCTGTATAGAGGC[A/G]CTAAGAGAAACAGAA	4703
rs570781439	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151616511	CCAGCCTGGCCAACA[C/T]GGTGAAATCCCGTCT	4703
rs570812712	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151561942	AGACTGGGAAGATCC[A/G]GCCCCAGAGCAGGAC	4703
rs570818658	snp	C/T	0.000399281	0.0141238	missense	NEB	GRCh38.p7	2:151569279	ATACCTCACTGAAGA[C/T]GTCCGCGGCATGTTT	4703
rs570838584	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151554109	AGTCAGGCTAACCAA[C/T]TCACAGCGAACAGTT	4703
rs570844805	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151645971	TGAGTACTAACATTT[C/T]GATATTCAATCTAAA	4703
rs570860340	snp	C/G	3.3484e-05	0.00409156	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151526182	CAGGTTGCTGACAGT[C/G]TTCGCCAGCAGGATC	4703
rs570882479	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151559542	TCTTGGAACCAACCC[A/C]AATGCCCATCAATGA	4703
rs570905221	in-del	-/TTAGGTATGCATTGCTT	0.00279162	0.0372561	intron-variant	NEB	GRCh38.p7	2:151543841	ATATTTCCCCTGTAC[-/TTAGGTATGCATTGCTT]ATGCTTCTTGGGACA	4703
rs570918442	snp	A/G	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151689261	CCAGGCTGGAGTACA[A/G]TGACACAATCTCGGC	4703
rs570924936	snp	G/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151514762	AACACATTAATGAGT[G/T]TCACTAGTGCAATTA	4703
rs570940080	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151733440	ATTGTAAAACGAAAT[C/T]GAGGTAAGGAAGTGA	4703
rs570962421	snp	A/C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151712949	TACTTGCAGTTGAAC[A/C/G]ATGGAAACTTGGAAG	4703
rs570989932	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151537476	AAATTTAACAGGCAT[A/G]CTTTCCTAGATAGTA	4703
rs570990335	snp	A/T			missense	NEB	GRCh38.p7	2:151694422	GTTTTTTTCATAGTC[A/T]TTCTTGTACATCACC	4703
rs570993272	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151712350	TAGGCATTGCATATG[C/T]AGATTTGTTAAGGAT	4703
rs571013769	snp	C/G	0.000399281	0.0141238	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151505482	ATGGCCACTACCGAG[C/G]TAATGTGCTTCTGCG	4703
rs571015530	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151628309	CACACTCCTTCCCAA[A/C]TCCAGCTCTGCTGGG	4703
rs571024419	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151720375	TCTGTGCCCAATAAT[C/T]GTAGAAGTTCATAGT	4703
rs571046551	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151628686	TCTCTACTAAAAATA[C/T]AAAAAATACTAAATA	4703
rs571049718	snp	A/G	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151618584	CCGATGAATAGTTAA[A/G]GTTCCTAGCATAGTC	4703
rs571070175	snp	A/C	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151502383	ATAAATAAACATCTA[A/C]ACATAAAAAAAAAAA	4703
rs571132358	snp	G/T	0.00557542	0.0525036	intron-variant	NEB, RIF1	GRCh38.p7	2:151515515	ACCACACTGAGTTTT[G/T]ACCTGTTTTTTAAAA	4703
rs571135539	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151676438	TCCACACTTGGGGCC[A/G]GCATTGTCTTTTAAA	4703
rs571153285	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151727569	GCCTATAATTTGCAA[A/G]ATAAGTTTTTGTTTC	4703
rs571159256	snp	C/T	0.00438332	0.0466095	intron-variant	NEB	GRCh38.p7	2:151660133	ATCGAAGTGGGGGTA[C/T]AAAGATCTAGCCATT	4703
rs571174587	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151659466	CTACCATGCCTGGCT[A/G]ATTTTTGTATTTTTT	4703
rs571176528	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151562335	ATAGGGTAGGCCTCT[C/T]ACCAGCTGGAAGGTC	4703
rs571189841	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151719743	AATTAGCCGGGTGTG[A/G]TGGTGTGCACCTGTA	4703
rs571195392	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151730829	CGTTAACAATCGTCT[A/G]GAACTTGCCTAATGT	4703
rs571212132	snp	A/G	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151559127	CATCAAAAAGTAGGC[A/G]AAGGATATGAACAGA	4703
rs571223810	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151649071	CCTTATTAAGTTCAG[A/G]TCTTTTTATCTCCTG	4703
rs571230045	snp	C/T	0.000399281	0.0141238	missense	NEB	GRCh38.p7	2:151723437	TCCGGGCTATCATTA[C/T]AGGGGTAAAACAAAC	4703
rs571243008	snp	A/G	0.00159617	0.0282053	intron-variant	NEB, RIF1	GRCh38.p7	2:151508610	TCAGGGCTCCCAGCT[A/G]TAGGACTGAGCCGGC	4703
rs571252686	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151680515	CCTTAGAAAGAAATG[G/T]CAAATGGCTAAAAGG	4703
rs571273099	snp	A/G	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151522118	TCAGAAATTGGGCCT[A/G]TTATGGATGTAGTAT	4703
rs571287692	snp	C/T	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151645907	TGATATGTATAACAA[C/T]GGACTGCAAGGAACA	4703
rs571292207	snp	A/T	0.000179533	0.00947282	missense, intron-variant	NEB	GRCh38.p7	2:151616103	CCAAAGCAAGTTTAT[A/T]GAGTTTCTGTAGAAA	4703
rs571319976	snp	A/G	0.00358779	0.0422022	intron-variant	NEB	GRCh38.p7	2:151686370	TAACAAATATTTATT[A/G]GGCATTTATTATGTG	4703
rs571320108	snp	G/T	0.00636936	0.0560724	intron-variant	NEB	GRCh38.p7	2:151693205	TTTCTTTTCTGCTAG[G/T]AATTAGGAAAGCAAT	4703
rs571332376	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151618096	AAAAGCACACAGTAC[G/T]TTTAACAATGGTTTA	4703
rs571355263	snp	C/T	0.00398564	0.0444627	intron-variant	NEB	GRCh38.p7	2:151572668	CTTGTGCCTCAGCCA[C/T]CCAAGTAGCTGGGAT	4703
rs571380556	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151494712	GGAGTGCAATGGCAC[A/G]ATCCCTGCTCACTGC	4703
rs571400578	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151549531	ATCATTCTATCAGGT[C/T]GAACCTTGAGGGTGA	4703
rs571422799	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151564325	ATGCCTGGCTAATTT[C/T]TGTATTTTTAGTAGA	4703
rs571436287	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151722087	GGCAAGATCAGACCA[C/T]AGATTCCATTAGAAG	4703
rs571437283	snp	A/G	0.0271762	0.113356	intron-variant	NEB	GRCh38.p7	2:151617491	AAAAAAAAAAAAAGA[A/G]AGAGAGAGAGAGAAA	4703
rs571443638	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151501809	TGAGTTGTTGGTAAC[A/G]TTAAATTAGGGAACC	4703
rs571444956	snp	C/G	1.78535e-05	0.00298771	missense, intron-variant	NEB	GRCh38.p7	2:151609830	CTGCAGGTCATAGGC[C/G]TTTTTTGCTTGGATA	4703
rs571451076	snp	C/T	1.67744e-05	0.00289602	missense	NEB	GRCh38.p7	2:151717499	GAGCTTGCTGTTCAG[C/T]GAGACCTTTTTTGTA	4703
rs571458319	snp	A/G	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151673707	CTCTGCAGGGCATGC[A/G]TGCTTTCTAAAAATT	4703
rs571459517	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151486868	AGGGGATGGAGAATG[A/G]ATGCCAATGGGCACC	4703
rs571467230	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151522021	TGAAGCTTTTTCCCA[C/T]TAACCATGGGAGCTA	4703
rs571471196	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151702058	CCCAGAGATTCTGGT[A/G]TGTTGTGTCTTTGTT	4703
rs571472421	snp	G/T	3.58764e-05	0.0042352	intron-variant	NEB	GRCh38.p7	2:151625516	GCCAGACCAAAGAAA[G/T]AAAACAAATGATCTT	4703
rs571487406	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151709557	AGTTCCCCCAAGAAC[C/T]ACTCCTCCCCTTTTT	4703
rs571488755	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151673021	CATAGGGTTTCATAG[C/G]TTTCGATTTAATATG	4703
rs571494549	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151552547	TCAGTGCTTTCAAAC[A/G]CACCAACTCTGGTTT	4703
rs571497125	snp	A/G	7.58769e-05	0.00615895	synonymous-codon	NEB	GRCh38.p7	2:151724278	GCTGAACATGGCGGT[A/G]TTCTTAACGGCCTGG	4703
rs571516269	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151609176	CCAGCCTGGGCAACG[A/C]GAGTGAAACTCCATT	4703
rs571600251	in-del	-/A	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151578504	CCTCTACTAAAAAAT[-/A]AAAAAAATCAGCCGA	4703
rs571603783	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151499877	TATGTGGCATTGTCT[A/G]TTTTCCACAGTATCT	4703
rs571656835	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151550774	CTCCCAAGTAGCTGG[A/G]ACCACAGGTGCATGC	4703
rs571664412	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151557121	TAGATAGACTGCTAG[C/G]AAGACTAATAAAGAA	4703
rs571669097	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151630491	AATACTACTCAGTCC[C/T]ACTGACTCACTGGAA	4703
rs571680679	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151692002	AAAATAGATCATGAT[G/T]GTTATGGCTCTCAAA	4703
rs571681151	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151729823	GGAACCCATCTTCAC[C/T]TTGTAATACTTCAGG	4703
rs571683473	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151678431	GAGGTTGAGATGGGG[C/T]ATTACCATAATTTGT	4703
rs571713476	snp	A/G	4.13548e-05	0.00454705	missense	NEB	GRCh38.p7	2:151664853	TTGTTCCATTTTTCA[A/G]TGTAGAGCCTCTGCA	4703
rs571741519	snp	A/G	2.71743e-05	0.00368597	intron-variant	NEB	GRCh38.p7	2:151671270	AAGATACCCTGGAGA[A/G]TATTCAAGGGATGTT	4703
rs571743708	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151513301	AAATAAGGCCAAGAT[A/G]TCGAGTTTGCCCCAG	4703
rs571765240	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151567675	TAAAAATAGAAAAAT[A/G]TTCTGCTGAGATAGC	4703
rs571768496	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151638134	AGATAAATTACCAAA[C/T]GCATAAATGCAGGAT	4703
rs571772483	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151652666	TTCATTAAATACTTA[G/T]AAAATTGTTTTAATT	4703
rs571786873	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151578970	CCTGTAATCCCAGCT[A/C]CTTGGGAGGCTGATG	4703
rs571792954	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151698930	TTGTGCAGGTTAGTT[A/G]CATATGTATACATGT	4703
rs571799428	snp	A/C	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151528617	ATATGTCCCCTCTAG[A/C]ACTAGTGGGTACTAA	4703
rs571808208	snp	C/T	0.000399281	0.0141238	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151513606	TATCAGTAGCATTCC[C/T]GGCCCTCATAAAATC	4703
rs571809291	in-del	-/GAGA	0.00119737	0.0244387	intron-variant	NEB, RIF1	GRCh38.p7	2:151510586	TAAGATATTCTGAGG[-/GAGA]GAGAGAGACCACATT	4703
rs571816267	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151543785	TACCACTGTGCTTGG[C/T]CTCTATGCCATTTCT	4703
rs571821120	snp	A/C	0.00159617	0.0282053	intron-variant	NEB, RIF1	GRCh38.p7	2:151520043	CTAATGCAAAACAAA[A/C]AAAAAAAAAAATGGA	4703
rs571828232	in-del	-/A	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151667360	TACGTCACAGTTTTT[-/A]AAAAAAGAATTTTCT	4703
rs571830632	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151658377	TCCCAGAGATTCTTA[C/T]TGATGCAAATAAGAG	4703
rs571839830	in-del	-/CTTGGTT	0.00438332	0.0466095	intron-variant	NEB	GRCh38.p7	2:151662712	CTTATAAAAATTCCC[-/CTTGGTT]AAGTCCCCTTGGTTA	4703
rs571868690	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151651863	TGCTTTTTAAAAAGC[A/G]GTGCCATAGATTTTG	4703
rs571889715	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151692636	GTCTTTTTTTAAATA[A/T]TTTTTTGTCTTAAAG	4703
rs571891007	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151698241	TAACAGCTTTATTGA[A/G]ATTTAATGCATATAC	4703
rs571935637	snp	A/G	0.000287972	0.011996	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151493411	GGAGTAACAGGTGTC[A/G]GAGTTGCTTTTCTCA	4703
rs571940509	snp	G/T	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151630605	GTTGGATGAGTGGAG[G/T]GTTAAATGAAAGAGC	4703
rs571949102	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151707989	AAGCAGATTCACAAA[A/C]TTTACTCTCCCCCTA	4703
rs571962441	snp	C/T	0	0	intron-variant	NEB	GRCh38.p7	2:151557459	GAGGAGCTGGTACCA[C/T]TCCTTCTGAAACTAT	4703
rs571975658	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151542925	TACCAGCATCCTTCC[A/G]CACCCTCCATGTGCT	4703
rs571982094	snp	A/G	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151671987	TTGAGTTAATAAAGG[A/G]AAAAAAAAAACACCT	4703
rs571984726	snp	C/T	0.00438332	0.0466095	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151506424	TGTCAGTATCAGTGA[C/T]TCAGACCAGTTATAC	4703
rs571988370	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151551096	CCTCAGCCTCCCAAG[C/T]AGCTGGGATTACAGG	4703
rs572010543	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151706417	TGCTTTAAATTGAAC[A/G]GCTTAGTCGGGCTCT	4703
rs572013399	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151494788	TGAGTAGCTGGGATT[A/G]CAGGCGTGCACCACC	4703
rs572020755	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151729317	CTGCTGTTGGAGAAT[G/T]GTGATAGCCACTGAC	4703
rs572030936	in-del	-/T			intron-variant	NEB	GRCh38.p7	2:151617727	TTATAGCACACAGTA[-/T]TTTTTTTTTTTTTGA	4703
rs572032031	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151573408	TGCCACAGATGCCTA[C/T]GGATTGAGTGGGAAG	4703
rs572052807	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151636631	CTAAATATAAAAAAA[A/T]TTAGCTGGGTGTGGT	4703
rs572058727	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151527355	CCCCCAACCATCCTC[C/T]TCTCCTTCTCGGATC	4703
rs572065448	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151622664	GCCTTCATCCTTGAA[C/T]ACTTTACCATGTATC	4703
rs572075529	snp	A/T			missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151519719	CTGTCTTTTGGATTG[A/T]ATTTTGGTGTCTTGC	4703
rs572079091	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151637064	CCTGTGTCTCTGACT[A/G]TGCGGGGTACTTGGG	4703
rs572091314	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151630272	GATAGAGAACACTTC[C/T]TCCTTATGCCTAAGG	4703
rs572094934	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151626973	TGACATATAGCCCTG[G/T]CTTATTTTCCTACAA	4703
rs572099716	snp	A/G	1.76275e-05	0.00296874	synonymous-codon	NEB	GRCh38.p7	2:151563850	CAGATCAGCATGCTT[A/G]GCTCCAACAATGGGA	4703
rs572100388	snp	C/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151491325	TAAACTTCCTTGATG[C/G]AATAGAGCTCAGGAA	4703
rs572112088	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	NEB, RIF1	GRCh38.p7	2:151497575	ATTTTAAATCATGAA[A/G]GTTTTCAAAATCATT	4703
rs572130630	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151621228	TTCAGCAAGTTTTAA[C/T]ATCACAACCTCTCTT	4703
rs572148392	snp	A/G	0.00199481	0.0315187	intron-variant	NEB, RIF1	GRCh38.p7	2:151500106	ATAATTACAACCCAC[A/G]GGGAAAACAATGAGT	4703
rs572151183	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151728065	TGGCACACTGTAGCC[A/G]TATGAAGGCACATTA	4703
rs572169293	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151620469	AATTTTTAAGATGTC[C/T]AGGGATCTGATGTTT	4703
rs572199977	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151731158	AGTTTAAAAGCAGCT[C/T]CTTGGAAACCATTCA	4703
rs572204300	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151571046	GTTTCGCTCTTGTTG[C/T]CCAGGCTGGAGGGCA	4703
rs572205688	snp	A/C/T			upstream-variant-2KB	NEB	GRCh38.p7	2:151735487	TTATGTGACAGAGAA[A/C/T]TGCTCTTTCTCTGGG	4703
rs572217916	snp	A/C/T	3.55714e-05	0.00421716	intron-variant	NEB	GRCh38.p7	2:151664622	TTCTAAACAATAAAA[A/C/T]AGAAAAACAACAGCA	4703
rs572230636	in-del	-/T	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151649919	TTCAAAGAAAAACAG[-/T]TTTGTTCGATCATTT	4703
rs572244289	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151714308	TACTGTCATAAACCA[C/T]TGTTCGCTTTGTGGG	4703
rs572249041	snp	C/T	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151658804	GCCTGTTTCTTTCTA[C/T]CAAATCTCTCAATTT	4703
rs572259723	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151651082	CATGCCACCTCATCC[A/G]GCTTCAGTTTGCCTT	4703
rs572266556	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151696557	TTTGAATAAACTTGA[C/T]AAGTCATTGGATTTT	4703
rs572270270	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151492733	TTCAAAGAAGGGGCA[C/T]GGTATAATTTTGAAA	4703
rs572277679	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151698051	AGCCCGGGCGACAAT[A/G]CGAGACTCCGTCTCA	4703
rs572285102	snp	A/T			missense	NEB	GRCh38.p7	2:151672428	TGGCGTCAGGTAGGT[A/T]TGTGTAATGATGCAA	4703
rs572294892	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151616330	TTTCAACAAAAAAAT[A/G]TGGGGAAAAAATCAA	4703
rs572334924	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151715232	GTAGAAGGAAACATG[C/T]GGGAAATAACTTTAA	4703
rs572349033	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151643024	TCAATAAGAAGCACA[A/G]TACTTTAAAACCACA	4703
rs572364790	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151722257	GATTTTCAATATGGC[C/T]TCCCGCAAATCCAAT	4703
rs572387830	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151614100	AATACTTTGATAATG[A/G]TATTTCAATATGATT	4703
rs572390677	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151656788	TCACACTGACTTATG[C/T]ATGTACTTTGCTGTT	4703
rs572391597	in-del	-/AC	0.00438332	0.0466095	intron-variant	NEB	GRCh38.p7	2:151662713	TTATAAAAATTCCCA[-/AC]AGTCCCCTTGGTTAA	4703
rs572430179	snp	C/G	0.00279162	0.0372561	intron-variant	NEB	GRCh38.p7	2:151549144	GCCTTCTGTGAACTG[C/G]GCACAGAGGATAAGT	4703
rs572436771	snp	A/C	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151491971	ATGAGATAATAGGAG[A/C]TTTCTTGCACCTCTA	4703
rs572437765	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151705798	GAGCTGGAGGCCATT[A/G]TTCTAAATGAAGTAA	4703
rs572452659	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151663489	ACGTCATTGCTTATG[G/T]TCACTCATGGTTGCT	4703
rs572469655	snp	A/G	0.00119737	0.0244387	intron-variant	NEB, RIF1	GRCh38.p7	2:151505075	ACACACATGTTTTAT[A/G]TATATACACAAAACC	4703
rs572475180	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151712628	GACACAGGAGGAGGC[G/T]GGAGCTTGCTGGCTA	4703
rs572480524	snp	A/G	5.49476e-05	0.00524126	intron-variant	NEB	GRCh38.p7	2:151696602	GAAATGTTATCCCTC[A/G]TAATTGGGTGTCCTG	4703
rs572490312	in-del	-/AAAAGAAATCACAATGTCA	0.0019968	0.0315343	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151506610	TGGGGGAGGGATAAC[-/AAAAGAAATCACAATGTCA]AAAAGAAATCCATCT	4703
rs572507208	snp	C/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151494809	GTGCACCACCATGCC[C/T]GGCTAATTTTTGTAT	4703
rs572528608	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151720732	GTTCCTTTTCAACTT[C/T]GCTGTTTGTTCCCTC	4703
rs572576885	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151684584	TCCCAGAGGGAAACA[C/G]TGATAGGGTGCAAGC	4703
rs572608929	snp	G/T	0.0115144	0.0749975	intron-variant	NEB	GRCh38.p7	2:151702972	ATGGTCTTTACATTT[G/T]GGCATGATTTTGCAG	4703
rs572625026	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151691349	ACCCAACCTAAGACG[C/T]CCATCCAGTCACTGT	4703
rs572633888	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151717736	ATTCATTTCCATGCC[A/G]TGGTTTGCAACTGCA	4703
rs572642460	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151539353	ACTAACTGGCATTGC[C/T]TTTTTCTAACTAGTA	4703
rs572663193	snp	A/G	0.00318978	0.0398085	intron-variant	NEB	GRCh38.p7	2:151697798	GAGGCCAGGTGCGGC[A/G]GCTCACGCCTGTAAT	4703
rs572684337	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151607046	CAAGATATCAGGTAA[A/G]ATCTGATAAGATTTT	4703
rs572684413	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151532419	ATGTCAAAGATGAAA[C/T]AGGGATGTAAAATAA	4703
rs572690722	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151516661	ATGTTCTGTCAATTG[A/G]ATGGCATCTCATTGC	4703
rs572716576	snp	C/G	0.000185385	0.00962592	intron-variant	NEB	GRCh38.p7	2:151709812	TGGAAATGAACTATG[C/G]AAGAATTTCCATGAG	4703
rs572744443	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151640237	ATTCCTGTCGATAAA[A/G]GCAATGCTATTTGCC	4703
rs572755218	snp	C/T	0.00517822	0.0506191	intron-variant	NEB	GRCh38.p7	2:151704291	GGACATTTAAGTCTG[C/T]AGAGGTTACTGCTGT	4703
rs572757495	snp	C/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151502283	GTGTATACTGCTTGG[C/G]TGATGGGTGCACCAA	4703
rs572782313	snp	C/T	0.000361011	0.0134304	missense, intron-variant	NEB	GRCh38.p7	2:151581554	GCACGTTCACATTAG[C/T]CTTCTCTTTCTCCCA	4703
rs572797277	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151541148	ATGAAATACAGCTTC[A/G]TTTGTCTGCGGATAA	4703
rs572804368	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151647952	AATGTGATTATGTGA[A/G]TATGTTCTTATTCTT	4703
rs572813291	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151502169	GTGGGAACTAAGCTA[C/T]GAGGATGCAAAGGCA	4703
rs572822095	snp	A/G	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151647172	CTGGAGTGCAATGGT[A/G]CAGTCTTAGCTCACT	4703
rs572823953	snp	A/G	1.65638e-05	0.00287778	intron-variant	NEB	GRCh38.p7	2:151697342	CAAACAATTGTCTTA[A/G]AACTTACATCACTGT	4703
rs572841396	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151653812	CTCTATTCAGGAAGC[A/C]CTTTTGACATATGAA	4703
rs572844231	snp	C/T	0.00636936	0.0560724	intron-variant	NEB	GRCh38.p7	2:151702837	ATTTGCCAGTCTGTG[C/T]CTTTTAATTGGAGCA	4703
rs572870212	snp	C/T	1.78752e-05	0.00298953	synonymous-codon	NEB	GRCh38.p7	2:151552744	AAGCTTGTAGTCATT[C/T]CTTGTTTTCAACATG	4703
rs572883027	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151684156	GTACAACAATGTTAA[C/T]ATACTTAACACCACT	4703
rs572889252	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151527880	ATCATCTTCAGAATC[A/G]AGTACTTTTAATTTC	4703
rs572982909	snp	A/G	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151525038	CCCAAACCAATTCTC[A/G]CCACTAACTTTTTGA	4703
rs573000702	snp	A/T			downstream-variant-500B, intron-variant	NEB, RIF1	GRCh38.p7	2:151485258	TTTTTTAGTAATTTT[A/T]TGTACAATTTGCTTC	4703
rs573012090	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151681620	CGAAAACAAAACACC[C/G]AACAAGAAGTAAAAC	4703
rs573018729	snp	C/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151530014	CTCTCCTTCTGTGCT[C/G]CGGCAGTTATAGCTA	4703
rs573030690	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151637324	TGCAGAGGAAATCAC[A/G]TGAATCAAGGCACCA	4703
rs573036698	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151654411	ACTGCTGTTTAATAC[C/T]GCCTGGGCTTACTAT	4703
rs573036942	snp	A/G	1.71375e-05	0.00292719	missense, intron-variant	NEB	GRCh38.p7	2:151619477	GGTCATAGGCTTTCC[A/G]TGCATGAATGATGTC	4703
rs573041919	snp	A/T	0.021333	0.101051	intron-variant	NEB	GRCh38.p7	2:151701989	ATCTTTCCTGCTTTC[A/T]CTTGTGGGCATTTAG	4703
rs573046595	snp	C/T	1.65985e-05	0.00288079	missense, intron-variant	NEB	GRCh38.p7	2:151612208	ATTGTCAGGGCATTA[C/T]TCTTTGCTAGGACAA	4703
rs573047672	snp	C/T	3.52603e-05	0.00419868	synonymous-codon	NEB	GRCh38.p7	2:151567423	AGGATCATCTCTCAT[C/T]GTCGGGACACCAACA	4703
rs573056121	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151723827	AGTGCTAACACAATG[C/T]AAGGAGCCAGGAAGC	4703
rs573084437	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151574516	TTAAAAAATAAGAAT[C/G]GGTATTGGATTTTGT	4703
rs573104454	snp	C/T	0.0142736	0.0832652	intron-variant	NEB	GRCh38.p7	2:151583841	TTCTAATTTAAATGG[C/T]TTCAGTATGTTTTCT	4703
rs573107331	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151541270	TACCTGAGTAAAACA[C/T]AACCATAATTATCAT	4703
rs573135393	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151625109	GCATGTTAAATATTT[C/T]ACCTCATTTAGTCAT	4703
rs573151161	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151726738	TTTTAAAATCCTTTT[G/T]TACAGGGCTGGGCAT	4703
rs573164134	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151579128	AAACTGGAAACACTG[C/T]ACACATTAACAAATC	4703
rs573220419	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151694187	CATCTTCCTTTAGCA[C/T]CTGGGTGAAGCTTTC	4703
rs573227446	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151571036	TTGAGACGGAGTTTC[A/G]CTCTTGTTGCCCAGG	4703
rs573235868	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151659447	CTGGGACTACAGGCA[C/T]GCACTACCATGCCTG	4703
rs573252580	snp	A/G	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151528152	AACCCAGGCAGTCTG[A/G]CTGCAGAGGGGCTTG	4703
rs573293100	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151494448	CCAGGATAGGCACCT[A/G]CCCTGAAACCCTTGA	4703
rs573300250	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151521711	ATCCCATTGATTCCA[C/T]TTCAGTTTCTTTTTC	4703
rs573326074	snp	A/G	0.0111196	0.0737302	intron-variant	NEB	GRCh38.p7	2:151609525	CATTTTAATCCTGTG[A/G]CAATTGACCCAAGGA	4703
rs573342319	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151552096	TAGGTCTCAATGTTT[A/G]CACTCACTGGCGGGA	4703
rs573344158	snp	A/G	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151659663	GAGGATGTAAGATGG[A/G]AAGTAAAAATGTTTT	4703
rs573357125	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151680610	GGGGAATTCTACAGA[C/T]GCTTGTGTAATTGGG	4703
rs573360567	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151624927	TATTTTATTGTTCTC[A/G]GGCAATTTGAAATGG	4703
rs573362774	snp	A/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151501289	GTGATTAAAAAAAGA[A/T]TTTGTTAAATTGATT	4703
rs573391302	snp	A/C			intron-variant	NEB, RIF1	GRCh38.p7	2:151510945	AAGTTTGTGGAAACA[A/C]AAGCACCATCTCACC	4703
rs573393673	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151634298	ATTGGATTCTATACA[C/T]TAAAAGCATGTCAGG	4703
rs573399302	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151486557	TTGTACATCCATGTC[C/T]GTAGCAGCATTACTC	4703
rs573418460	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151687229	ATCAAGTACAAATCA[A/G]TAATTTCTCCCCTCA	4703
rs573437684	snp	C/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151513807	GTTGTCACAGATAGT[C/G]TCGCTTGCTACTCTT	4703
rs573452969	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151631514	AATGACCCAGAAATA[C/T]CTCCTAGCCATAATA	4703
rs573473619	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151731058	TAGAGTCATTCCTCC[A/G]GTCACACAAAACATC	4703
rs573487321	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151638539	TTACAGAGAGAAATG[C/T]TGTGACTCAATACAT	4703
rs573487443	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151488349	GGCTTTCCCCTTTAT[A/G]TTTTAAAATAATTGT	4703
rs573521385	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151717084	GAATTTAAACCAGCT[C/T]TTCACGGAAGTGTGT	4703
rs573536794	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151544304	GAGTTATCTTTACTC[C/T]GAAGCACTATAAGTT	4703
rs573537251	snp	C/T	1.71965e-05	0.00293222	missense, intron-variant	NEB	GRCh38.p7	2:151618471	TCAAGGTCTGACTTA[C/T]ACAAATTCTGCAGAT	4703
rs573541651	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151617602	ATTAAAGCTGCATAA[A/G]TTCCTTACCTTTGTT	4703
rs573552392	snp	C/G	5.6912e-05	0.00533411	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151514892	CAGTCAGGTTTCTGC[C/G]TTTAATGGACTCTTC	4703
rs573579322	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151653174	TCTTTCAAAGATTTT[A/G]ATTAAGAGGTCCTAC	4703
rs573579430	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151660189	CAGAGACACTTGAGA[A/G]CCCTCTGTGGGACTG	4703
rs573585650	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151528962	TTCTCAGCCACCCAC[C/T]GCAAAAGCTGAGTGG	4703
rs573613643	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151653791	TTAGAGGTCGTCTGG[C/T]CCGACCTCTATTCAG	4703
rs573628875	snp	A/G	9.97722e-05	0.0070623	intron-variant	NEB	GRCh38.p7	2:151541573	ATAAACCAAGTTATC[A/G]CCATCATTTCTGTTT	4703
rs573670215	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151722833	GGATTACAGGGGTGA[A/G]TCACCACATCCAGCC	4703
rs573677087	in-del	-/A	0.0505692	0.150756	intron-variant	NEB	GRCh38.p7	2:151581192	TTACAAGGAAAAAGC[-/A]AATGATGGATGGCCC	4703
rs573679607	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151578576	TGAGGCAGAAGAATC[A/G]CTTGAACCCGGGAGG	4703
rs573680669	snp	C/T	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151708985	CTAAGTGATGTAATC[C/T]TGCTTTCTCCAGCAT	4703
rs573685953	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151611920	GTAATGCAATTGTGA[C/T]GTCTCCAGGTCACTG	4703
rs573686432	snp	C/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151665903	ATTTTAAATATATTT[C/G]TATGCATATATATAA	4703
rs573693040	snp	A/T	6.69871e-05	0.00578697	missense, intron-variant	NEB	GRCh38.p7	2:151619734	ATGTGGTGACCCAAC[A/T]GTTTACGATATGCTT	4703
rs573713941	in-del	-/TTTTGTATCTATTGCCATGCTAAATCGATA	0.0023933	0.0345097	intron-variant	NEB, RIF1	GRCh38.p7	2:151488870	CTGGACTTCATCTAT[lengthTooLong]TTTTGTATCTATTGC	4703
rs573714322	snp	G/T	0.00993419	0.0697739	intron-variant	NEB	GRCh38.p7	2:151608874	TGCCATTGCACTCCA[G/T]CCTGGGCAACAAGAG	4703
rs573733338	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151646404	CTTGACTTATCTGGG[A/G]CATAACTGCCTTTCA	4703
rs573755765	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151693536	ATTTTCTGTTCCTGC[A/G]TTAGTTTGCTGAGGA	4703
rs573757030	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151651774	TTACATGATACCCAG[C/T]TTCATTATTACATAT	4703
rs573762770	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151565168	GGAGAGAAAACCAAA[C/T]CTTTTATTACTATAA	4703
rs573766756	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151694119	ATTAAGGAGATTAAG[A/G]AAAATTTGCAGTATT	4703
rs573812402	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151551347	TTGGGTAACATAGAA[C/T]AGGTAGGTTAAATAT	4703
rs573814642	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151559272	GTTAGAATGGTGATC[A/T]TTACAAAGTCAGGAA	4703
rs573822094	snp	A/G	0.000188142	0.00969719	missense, intron-variant	NEB	GRCh38.p7	2:151636285	ATGGCGTCGCTTCGC[A/G]AGTCATAGCCTTTCT	4703
rs573822657	in-del	-/CAGCCAAAGGAGAATAGGCTCCATGGGCAGGTTTGGGTTCTGAGCT	0.00398564	0.0444627	intron-variant	NEB, RIF1	GRCh38.p7	2:151527282	ATTTGTGTCCAGGCC[lengthTooLong]CAGCCAAAGGAGAAT	4703
rs573850843	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151730331	CACAAAGTGTGGGAA[A/G]GGTAGGCTGCAATTT	4703
rs573859524	snp	C/G	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151583223	ACTGAAATTTTCTAC[C/G]TAATTACATAGAATA	4703
rs573893870	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151623787	AATACTTTATTTATT[A/T]CATTTTTTCTTTAGG	4703
rs573898757	snp	C/T	0.00722012	0.0596484	intron-variant	NEB	GRCh38.p7	2:151581477	AAATGATGTGTGCTG[C/T]CTTACATTGCTGATC	4703
rs573903582	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151535028	AATCTGAAAATAGGA[A/C]ATTAAATACAACTTT	4703
rs573907541	snp	A/G	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151487258	AAAGCTATCCTCCAC[A/G]GTGTTAAAATTGTAA	4703
rs573910896	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151630457	AGTATTTTATCTGAC[A/G]ATCCTCTGAAGTGTC	4703
rs573926640	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151691573	GCTTCTCACATAGAA[C/T]TTGTTAAATAATGAA	4703
rs573927528	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151566451	GTTCAACATCTATGC[G/T]GCAGCAGTCTTTGAC	4703
rs573951853	in-del	-/TAAAT			intron-variant	NEB	GRCh38.p7	2:151692378	CTGTTAAAGGAAAAA[-/TAAAT]TAAACCAAAAAGAAA	4703
rs573971362	snp	C/G	0.00358779	0.0422022	intron-variant	NEB	GRCh38.p7	2:151660860	AATGTTCTGCATAAT[C/G]CAATATGGTAGAACC	4703
rs573971577	snp	C/T			synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151627613	GTAGTTCTTGTAGTC[C/T]ACATCGCTGACTAAG	4703
rs573996197	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151632072	ATTTCATTGTGCAGG[A/G]CCCCAGTCTCTTCCT	4703
rs573996296	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151534145	CATCCTTGCAGCAGA[C/T]GGGATGACATCTCAT	4703
rs574018891	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151730730	TAAGATGCAAAATTT[C/T]CCTCAATGGCCTGCA	4703
rs574033065	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151702704	CCCTGCCTTTTTTTT[A/G]TTTTCCATTTGCTTG	4703
rs574036198	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151652047	AAAGGAGGGCAAATA[C/T]GAAAATGTTTGAAGA	4703
rs574047897	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151641969	CCCTCCTCCCTCCCC[A/C]CATCCTATGACAGGC	4703
rs574053092	in-del	-/AA	0.00199481	0.0315187	intron-variant, utr-variant-3-prime, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151498170	AGAAGCAAAGAAGGG[-/AA]AAATGGGCTTCAAAC	4703
rs574074536	in-del	-/A			intron-variant	NEB	GRCh38.p7	2:151667038	TATAACTTAATTTGT[-/A]AAAAAAAAAAATTAA	4703
rs574074634	snp	C/T	0.00318978	0.0398085	intron-variant	NEB	GRCh38.p7	2:151694091	TATTTTTCCTCCTAA[C/T]AAAACAGAGGGCATT	4703
rs574100586	snp	A/G	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151697935	CCTGGGCATGGTGGC[A/G]GGTGCCTGTAATCCC	4703
rs574102907	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151722359	GCTGGTTTCAAGCCT[A/G]AGGACTCTGTTAAGC	4703
rs574103523	snp	A/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151542078	GTCACACTCATTGAG[A/T]CTACCAAGAACTTCA	4703
rs574142553	snp	C/T	0.00358779	0.0422022	intron-variant	NEB	GRCh38.p7	2:151686406	TGCTGGGTTCTGTGA[C/T]AGGAATAAAAACAAA	4703
rs574146967	snp	C/T	0.000145075	0.00851565	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151514820	AAGTGGGCACTACCT[C/T]GCTTGCTATTTTAGT	4703
rs574157563	snp	G/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151507449	AATAATTATCTGACC[G/T]TCATTTAAAGCAGGC	4703
rs574195456	snp	A/C	0.00279162	0.0372561	intron-variant	NEB	GRCh38.p7	2:151651402	AAATCAGGAAGATAC[A/C]TGACTAAGTAAATAC	4703
rs574197358	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151658585	CCTAGCAACTATGAT[C/T]AGGATGAAAAAGGAA	4703
rs574230816	snp	C/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151704826	ACCCGTCTTCTGCGT[C/G]GCTCGCTCACGCTGG	4703
rs574242986	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151727144	GTTTTAAAATTCCCA[A/G]GGGGTTCCAGTGTGC	4703
rs574256696	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151558604	TACCAAAACAGATAT[A/G]TAGACCAATGGAACA	4703
rs574286344	snp	C/G/T	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151644883	GGGAACATCACAGAG[C/G/T]GTACTTATGCAATCC	4703
rs574293654	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151529428	CAATGCTCCTTAAGA[C/T]GGAATTTTAAAAATC	4703
rs574309369	snp	A/G/T	3.31391e-05	0.00407046	missense	NEB	GRCh38.p7	2:151679752	CTGGCAGCTTTGGCA[A/G/T]CTCTGATGGGAATCG	4703
rs574315546	snp	A/C/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151522329	CTGAACTGAGAAACT[A/C/G]TATTAAATACCAATC	4703
rs574316948	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151572247	GCATCGCTTGAACCC[A/G]GGAGGCAGAAGTTTC	4703
rs574324297	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151627931	AAAATTGCTAATTCT[C/T]GCAGAGTAATGAAAG	4703
rs574356522	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151521658	CCTTCTGTCTTTTAG[A/G]AGATACTTGTTTCTG	4703
rs574363877	snp	G/T			missense	NEB	GRCh38.p7	2:151675359	CATGGTGTATTTATG[G/T]TTCACATCTTCTCCT	4703
rs574366255	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151640928	CTGTTAGAATTTAGA[A/G]TTTGTTTTTAAAATA	4703
rs574369613	in-del	-/AAAT	0.021333	0.101051	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151498920	TCAAAATATCTGTAC[-/AAAT]AAATAACAGTAGAGA	4703
rs574373511	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151689551	ACTTTATTTAAATTT[G/T]TTAAAAGGTGACGTT	4703
rs574385575	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151569443	GCCTATCCATTGGTC[C/T]CATGAAGAAATACAA	4703
rs574386664	in-del	-/C	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151636034	CAGAAGACGCTGTGT[-/C]CCTGTAGGTTACAGA	4703
rs574395938	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151521038	AAAACTGAGCTGTTT[C/T]TAGATGTTAGCCAAC	4703
rs574430935	in-del	-/CTTTT			intron-variant	NEB	GRCh38.p7	2:151671681	ATAAATTGGGCTTTC[-/CTTTT]GATTCCACTGAAGAC	4703
rs574435543	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151530721	CCCAGCTCCCAGCCC[A/G]CAGCCATCACCAATG	4703
rs574438811	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151648956	AGGCCTGAGAGCTCC[A/G]TGTTTCAGCATTCCC	4703
rs574451516	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151707132	ATTTTATAAACAAAA[C/T]ACTCATAGTAACTCT	4703
rs574454612	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151662884	TCTACACCTGTGCCA[C/T]GGCTGCTTTCATTCA	4703
rs574456460	snp	C/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151539424	TGGAACTGAGATATT[C/G]TTCACATTTGCTGTG	4703
rs574477731	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151489663	CAGCGTCCCAAAGTG[C/T]TGGCATTATAGGCAT	4703
rs574519394	snp	A/G	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151674163	TCATTTGAATTTAAT[A/G]TGGTAATGTCAGTCA	4703
rs574520488	snp	A/C/T	3.37982e-05	0.00411074	intron-variant	NEB	GRCh38.p7	2:151612152	AATCTGTGGAAGGTA[A/C/T]GATTCTGGCAACAGA	4703
rs574524843	snp	G/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151504553	ATGAGATCTAAATAA[G/T]ATGAACAACCTGCAA	4703
rs574534331	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151525424	ATTCTAGTTCTTCTC[C/T]GTCATTTGTGTCCTG	4703
rs574544074	snp	A/C/T	4.96868e-05	0.00498411	synonymous-codon	NEB	GRCh38.p7	2:151680787	TGGAGCATCTTCAAT[A/C/T]GAGGTAAACTTGAGG	4703
rs574547229	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151500890	AGGTGTGAGCCACCA[C/T]GCCTGGCCCCAAATA	4703
rs574564577	snp	A/T	0	0	intron-variant	NEB, RIF1	GRCh38.p7	2:151524121	GTAAAGTGGAGAACA[A/T]GAAAGGTCTAGACAG	4703
rs574565073	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151683859	AAAATATGGCATATC[A/G]ATACAATAGAATATT	4703
rs574571582	snp	G/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151511712	AAGGCCTATCCCAGG[G/T]TGTGAAGGATGGCCT	4703
rs574602169	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151648028	TCTCATATAGATATA[C/T]AGATATAGATCTGAG	4703
rs574636914	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151689911	GTATGAGCTAATTTG[C/T]GTCATTAAAATATAT	4703
rs574647086	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151642192	TGAGTAATGTGTCCT[A/G]TAATTCAGCCCTTGT	4703
rs574649870	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151547009	CAGATTGAATGGATT[A/G]GTCTTTTAGGAGGAG	4703
rs574677745	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151715430	CCACCCCCCAAATTC[A/G]TATGTTGAAGACCTA	4703
rs574681426	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151675486	TCACCCATGATTTTC[C/T]AGTGTTAAAAATCAT	4703
rs574693122	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151704659	TTCTTTGAGTCGGAA[A/C]GGTAACTCTCTGACC	4703
rs574715843	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151617799	GGGCACGGTGGCTTA[C/T]ACCTGTAATCCCAGC	4703
rs574720296	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151509563	GAGGGTTGGACTGCT[A/G]TTTCTCGTGGCCCAA	4703
rs574746662	snp	C/T	0.00115963	0.0240514	missense	NEB	GRCh38.p7	2:151567260	AATTACGATAATCAA[C/T]ATCACTGACAAGGGT	4703
rs574756435	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151674664	TGTTCTTTTCCAGAC[A/C]GAAGTTGAAGGAATC	4703
rs574757972	snp	A/G	3.31285e-05	0.00406978	intron-variant	NEB, RIF1	GRCh38.p7	2:151518301	GCCAGAGGAAAAATC[A/G]GTCTTGATCCACTTA	4703
rs574785257	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151554116	CTAACCAACTCACAG[C/T]GAACAGTTGGGGGCA	4703
rs574822994	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151616821	CTCTATTCTGTTTTA[C/T]GAAAAACTCAATGCA	4703
rs574825401	snp	A/G	6.89774e-05	0.0058723	intron-variant	NEB	GRCh38.p7	2:151553538	GGATCAGAAAAAAAA[A/G]ATTGACCATAATAAC	4703
rs574836604	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151724782	GATCAGGCCTGTCCA[A/G]TTTTCTCCTATAAGA	4703
rs574848193	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151515990	AAAGAAAATTTAGTG[C/T]TTCTGCTTACAATTC	4703
rs574906895	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151611600	AGTCTAAAATATGCA[A/T]ATTAAGGGCTGACTC	4703
rs574918728	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151611653	AAATTTTGGATGAAA[C/G]AAATGATCATCTATC	4703
rs574922237	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151633358	TTTCTTTTTAAAGTA[A/G]AAACGTTTCTTCCTT	4703
rs574925585	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151505862	TATGCCCAGCAGGTC[A/G]TTTGACTAGGATAAA	4703
rs574939161	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151721261	GATTCTATTTTTATC[A/C]TGCTGTTTTCCGCTC	4703
rs574949083	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151510349	AGGCCTAGCCGAAAC[C/T]TTTGGTGGGCTTTTG	4703
rs574960576	snp	A/G	0.000221967	0.0105325	intron-variant, utr-variant-3-prime	NEB, RIF1	GRCh38.p7	2:151497758	AAAACAACCATGAGT[A/G]ACATTTCATTTCTTG	4703
rs574967543	snp	A/C	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151731308	AGAGCTGTGCCACTA[A/C]TTAGATAGTGCATCC	4703
rs574990727	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151559888	GGCATATGTATACCT[A/G]TGTAATAAACCTCCA	4703
rs574997115	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151611083	ATGGTTTCATAATTA[A/G]TATGAAGCAATATAA	4703
rs575036921	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151668035	AAGACAATCTATGAA[C/G]TTAGGACTATTAGTT	4703
rs575041402	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151718551	ATAGAGTGAAGAAAC[A/G]CTACACACTTATCTT	4703
rs575043770	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151667630	ACTCCTGGGTTAAAG[A/T]GATCCTCCCATCTCA	4703
rs575054196	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151733568	TCAGAAGAAGCTGAA[A/G]TTTATCCCCCAGCAC	4703
rs575057605	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151718552	TAGAGTGAAGAAACG[C/T]TACACACTTATCTTC	4703
rs575091306	snp	A/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151503540	AAACTCATAAAAACA[A/T]TCTAGCTCTCAAATA	4703
rs575092904	snp	A/C	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151495471	TAATGTTTTAGAAGC[A/C]CTGTACTCAAGTACT	4703
rs575108565	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151619092	ATATGCTTTCCCTCT[A/G]TCTCCCTACTGCCCT	4703
rs575115630	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151704635	TTTCCAGGTGCGTCC[A/G]TCACCCCTTTCTTTG	4703
rs575133539	in-del	-/CTTG	0.00358779	0.0422022	intron-variant	NEB	GRCh38.p7	2:151703409	TGAACGTTGGCCTGC[-/CTTG]CTAGATTGGGGAAGT	4703
rs575135001	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151634160	CATGTAATTGTAGTA[C/T]ATACCCCAAATCACC	4703
rs575150573	snp	A/C	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151488839	TGCTGATTTATAATT[A/C]TTTTAGGGTCTGTTT	4703
rs575160299	snp	C/T	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151547068	GCAGCAAGAAGTTGC[C/T]AATGAGGTCAGAGTA	4703
rs575162285	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151533694	GAAGACATCAAATAC[A/G]TTATAATGTGAAGCA	4703
rs575174530	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151725326	TGGTTCATGCTTTTC[C/T]AGATTTGTGAACTAG	4703
rs575186265	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151732839	AAGTGGGGAAGAAAG[C/T]AGTTTTAGAAGACGA	4703
rs575199748	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151675738	TCTTCCATTTTTGTT[A/G]GTTTCTATTTTTTTA	4703
rs575227042	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151687321	GAATGTGATGTGAAA[A/G]AGCCCATGCTCATGA	4703
rs575237517	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151512699	TTCTTTCATGATTGG[A/G]GTTTATGAGTGATGG	4703
rs575246159	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151535872	GCTGTTTATCATATG[A/G]TATAATTGTGATAAT	4703
rs575248859	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151565985	TTCTTGAGGCTGTTA[C/G]TGTGCATGAGGCACT	4703
rs575287494	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151686846	TACATGGCCCATAGA[C/T]GAGCCTTAAGCAACC	4703
rs575343794	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151704499	TCAGACTGCTGTGCT[A/G]GCAATCAGCGAGACT	4703
rs575357270	snp	G/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151530020	TTCTGTGCTCCGGCA[G/T]TTATAGCTATTATCA	4703
rs575377770	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151715739	AAGCCACCCAATGTA[C/T]GGTATTTTGTTGTAG	4703
rs575378799	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151517322	GCACTGCTCAATCTC[C/T]GAGCTCTTGGGTTGT	4703
rs575395962	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151537413	CTTTGGTATATTGTT[G/T]TATAACATATGGAAG	4703
rs575407079	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151717877	TTTTTTTTTTGAGAC[A/G]GAGTCTCACTATGTT	4703
rs575415587	snp	C/T	0.00119737	0.0244387	intron-variant	NEB, RIF1	GRCh38.p7	2:151525330	GGAACAGAGTTGGTT[C/T]ACTTGAAGAACTGTG	4703
rs575426263	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151674834	GGATCCAGAGAAAAA[A/C]AAATAAAGGTTCTGG	4703
rs575441385	in-del	-/A			intron-variant	NEB	GRCh38.p7	2:151564319	CCACTATGCCTGGCT[-/A]AATTTTTGTATTTTT	4703
rs575491723	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151529474	ATACAGCCATGCAGA[A/G]ATGCACCTTCCTATC	4703
rs575499014	snp	A/G	0.000149037	0.00863114	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151524540	TGTTTGGCTGCCTGT[A/G]TGGCCTTCTTGATGT	4703
rs575502115	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151682413	TAAATGAATGGTTAA[C/T]GTAAATGGTTAACAA	4703
rs575551386	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151573750	TTCTGAGGTCATACT[A/G]TTCTACACACAAGTA	4703
rs575565098	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151688555	CAAACTTTCATCCCC[C/T]ATTTCAGGGACTGTG	4703
rs575570267	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151717279	GCTTTTGCTGTAGAG[A/T]CTTTGGGGATCATAT	4703
rs575604630	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151693459	TGTGTGTTGCACCCC[C/G]CATGTATCCATGTGT	4703
rs575621498	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151684520	CAATGTTTTTGATTT[A/G]TTTCCATTTTACAGA	4703
rs575662770	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151522763	GTACATTAATTTTCT[C/T]AAGATGCCTCATCAT	4703
rs575672064	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151646342	AAACATTATACAGAA[C/T]TGATATAATAAGCAG	4703
rs575683350	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151684061	TTGCCACAAGCTAGG[A/G]GAAGAAGGAAAATGG	4703
rs575688720	snp	C/T	0.000754717	0.019411	intron-variant	NEB	GRCh38.p7	2:151581449	TGGTTAGGCAGAGAG[C/T]ACTGTGAAAAGCAAA	4703
rs575701990	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151526759	TGCTGCCCTGCTTGA[C/T]TGCTGGCGCCCCTCA	4703
rs575732128	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151572936	CTAACTTTGAGAACA[C/T]GGGAAAATTTCTTAA	4703
rs575741197	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151526399	ACTTGCAAATTTTGG[A/G]AAATATTCAAAAGGG	4703
rs575748655	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151639468	CACAAAAACTTTATA[A/T]AAAAAAAGAAAAGGT	4703
rs575774513	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151626576	GAATCTTGCTCTGTC[A/G]CCCAGGCTGGAGTGC	4703
rs575784920	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151638676	GGAGGGGTACCTTTG[C/T]ACTAGGGTGGAGGCT	4703
rs575789994	snp	G/T	0.00119737	0.0244387	intron-variant	NEB, RIF1	GRCh38.p7	2:151494860	TCACTATGTTGGTCT[G/T]GCTGGTCTTGAACTG	4703
rs575820785	snp	C/T	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151617827	AGCACTTTGGGAGGC[C/T]GAGATGGGTGGATCA	4703
rs575857499	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151625879	ACACACACACATATA[C/G]ACACCCACGTGTGTG	4703
rs575861609	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151673479	AAAGTTATACTGTAG[A/G]CTTTCACTTTCTACT	4703
rs575865769	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151684614	CCAGATCAGTTCTTC[C/T]TAACCTTGAAGGGCA	4703
rs575892313	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151705960	AGTAAAGACTACATA[C/T]TGATCATAGTGTACA	4703
rs575900829	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151549997	TCCTGGCCAGGTGTG[A/G]TAGCTGACATCTGTA	4703
rs575901416	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151727976	GTGATCTTAGTATAT[A/G]TTAGTCTAACTTCAA	4703
rs575930999	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151549535	TTCTATCAGGTTGAA[C/G]CTTGAGGGTGAGACT	4703
rs575958060	snp	C/T	6.17354e-05	0.00555553	missense	NEB	GRCh38.p7	2:151562636	ATCTCCTGGGCGTTT[C/T]GGACGCGTATAACAT	4703
rs575965243	snp	C/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151563225	TCACCATGTTGGCCA[C/G]GCCAGTCTCGAACTC	4703
rs575966196	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151556659	TGAAAGAAGAAGAGC[C/T]AACTATCCTAAATAT	4703
rs575967856	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151713620	TTTGTGGATCTGGAA[A/G]GGAGCAGAGAGGCAG	4703
rs575974234	in-del	-/TTC	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151680498	AGTCCCTCTTACCTT[-/TTC]CTTAGAAAGAAATGT	4703
rs575979401	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151508951	CTTTCATCATCGCTT[A/G]TCACTGTCCTTTCAC	4703
rs575983497	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151512621	ACCTGGTGAATCTCT[C/T]TTTTATTGGGAAAAA	4703
rs575985689	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151512132	GCCTCCCGGGTTCAC[A/G]CCATTCTCCTGCCTC	4703
rs575992442	snp	C/T	0.000161721	0.00899078	intron-variant	NEB	GRCh38.p7	2:151570069	GTTCAACCCCAAATG[C/T]AGCCCACTCACATCG	4703
rs576011710	snp	C/T	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151632263	TTGGAAAGATTTCAC[C/T]TGTCACAGAAACTAA	4703
rs576028439	in-del	-/A	0.00755907	0.0610114	intron-variant	NEB	GRCh38.p7	2:151726285	TGGCAATATATTGAC[-/A]AAAAATTCTATCCTT	4703
rs576037795	snp	C/T	0.00358779	0.0422022	intron-variant	NEB	GRCh38.p7	2:151566959	TTAAAAAAATTTGAT[C/T]GAAAGTTACTCAGAA	4703
rs576039712	snp	A/G	0.00046853	0.0152986	intron-variant	NEB	GRCh38.p7	2:151690863	ATGAAATATCAGTAT[A/G]TTCTTGGTTATACAT	4703
rs576055505	snp	C/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151720713	CATGACATGGCATTT[C/G]CTGGTTCCTTTTCAA	4703
rs576067859	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151642444	ACCATTATTTTAAAC[C/T]ATTCATCGAAACAAT	4703
rs576068953	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151663026	ATCAAATGGACTCTT[G/T]AGCTAAATTCTTGGC	4703
rs576076237	snp	A/G	0.000629765	0.0177337	missense, intron-variant	NEB	GRCh38.p7	2:151650265	TGTCTGGAGGCTGAC[A/G]ATATTTCTTCTCACT	4703
rs576094056	snp	C/T	1.65762e-05	0.00287886	missense, intron-variant	NEB	GRCh38.p7	2:151627821	TGCTTGCGGTAACCA[C/T]CTTTGTATTTGTACT	4703
rs576097741	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151569550	AGGCAGTGTGACAAA[C/T]GATAGCATATATTTT	4703
rs576098387	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151503727	CAATGAGAAAAATCT[A/G]ACCATTTTGTTGCAT	4703
rs576142462	snp	A/G/T	0.00031536	0.0125534	missense, synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151636314	CTTCTTTGCTTCTTC[A/G/T]TTAGCAAGTTTGTAC	4703
rs576163234	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151665866	TCATAGACAACATCA[C/T]ATGTTTGGGTCTAAT	4703
rs576167442	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151547847	AGGGGAGGAAATATC[A/G]AGGATATAGAAAATG	4703
rs576177807	snp	A/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151615348	GAGGGAAAGTCTGGA[A/T]TTGAGTCCTAAGGAG	4703
rs576184961	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151734310	TAATTTCCTCAGTTA[G/T]GGCCCAAACCTTTGA	4703
rs576192217	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151706796	TGTATTTGCAAAGTT[A/G]TATATTCATTTAGTC	4703
rs576212927	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151622576	TCTTTATGTGTTTGT[A/G]TATTTCTTCATTTTA	4703
rs576220399	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151670536	GTGGTCTCAGAATGA[A/G]ATCCCAGATGACTGC	4703
rs576222548	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151621556	GTTCGAGGACATGAG[A/G]GTAGCAGGTACCAAA	4703
rs576224678	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151704602	AAAAGCGCAATATTC[A/G]GGAGGGAGTGACCCG	4703
rs576226396	snp	A/T	2.6371e-05	0.00363109	synonymous-codon	NEB	GRCh38.p7	2:151664567	AGGCCTCAGGTCATA[A/T]CCTTTCTTCTTTTCC	4703
rs576247324	snp	A/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151577328	CCTGATCACACAGCC[A/T]GTCTTTCAATTCGTA	4703
rs576254823	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151720973	TCCTTCAATCATCTC[A/G]ACTCCATTTCTCTTT	4703
rs576281961	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151728597	CAACAGTCCTATCTA[C/T]GTAGTAGGTGAGAAA	4703
rs576286059	snp	A/G	8.35652e-05	0.00646341	synonymous-codon	NEB	GRCh38.p7	2:151671188	AATAGGGATCCATCC[A/G]ATGCCCTTCAAGAAG	4703
rs576294918	snp	C/T	0.00318978	0.0398085	intron-variant	NEB	GRCh38.p7	2:151712761	CATGTGGGACCCTCT[C/T]TACCAGCGAAGGGGT	4703
rs576306653	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151663404	GTTAAAGGACATGAA[C/T]TCAATCTAAGGTAAC	4703
rs576311412	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151498472	AGGAAGAGAAATACC[A/G]GAAGCTTTTAGACTC	4703
rs576312700	snp	A/G	0.00119737	0.0244387	intron-variant	NEB, RIF1	GRCh38.p7	2:151531543	GCTGGTCTCAAACTC[A/G]TGGCCTCAAGTGATC	4703
rs576341516	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151656742	CTGCTGAGGCCACTG[A/G]GGATTAGAACCCAGA	4703
rs576352358	snp	A/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151496818	AGGAAAAAAGGATAA[A/T]TTTGCTAAAGAAAGA	4703
rs576359540	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151719797	AGTGAGAGGATCACT[C/T]GAGCCTGGGAGGTGG	4703
rs576375058	snp	C/T	0.00279162	0.0372561	intron-variant	NEB, RIF1	GRCh38.p7	2:151505822	TATTTAGACTGCAGC[C/T]CTTTCCTGTATACTC	4703
rs576423557	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151669531	CTGCAGAGGTAACAT[G/T]TACACTCAAACTTGG	4703
rs576442482	in-del	-/AG			intron-variant	NEB, RIF1	GRCh38.p7	2:151522702	GAATCAGAGGAAGAC[-/AG]AAATAATGGCTTGCT	4703
rs576443058	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151568938	AGGAAGTTTGCTTAG[C/G]TCTCAAAGTTATATA	4703
rs576457241	snp	C/T			synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151609995	CTTTTGGAATTCCTT[C/T]TTGTACTCCCTTTCA	4703
rs576480071	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151711687	CTCAGCCACAAGTGC[C/T]GGCAATAATATTTAC	4703
rs576514493	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151712464	TGTAAGATCACTCAA[A/C]CCCCTCATCCAAAGT	4703
rs576518579	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151639646	TTTTGATAAAATATG[C/T]TACTTTATCAAAATC	4703
rs576537316	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151696570	GATAAGTCATTGGAT[C/T]TTATGTATAGAGTTA	4703
rs576556678	in-del	-/A	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151636799	AAAACAAAACAAAAC[-/A]AAAAAAAAAGATACC	4703
rs576575365	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151696447	GTTTCCTTCACAGAA[C/T]TGTTTCACTGTAAAT	4703
rs576575471	snp	G/T	0.00358779	0.0422022	intron-variant	NEB	GRCh38.p7	2:151689595	GGAGTGTAAAGAACG[G/T]ATGAGGCTGTTTAAT	4703
rs576589999	in-del	-/CTTAA	0.00597247	0.0543191	intron-variant	NEB	GRCh38.p7	2:151633561	CATGGACCAATCAAT[-/CTTAA]CTTGAGTAATGGATT	4703
rs576600477	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151720812	CTCTGCCCTTGGCCA[C/T]GCACTCTTCTGCTTC	4703
rs576631368	snp	C/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151613439	CAGTGAACTTGGATA[C/G]AAAAAATATGTAACA	4703
rs576634277	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151713496	GGCCTGGGCCTGGTA[G/T]CCTCATGCTGTGTAA	4703
rs576634292	in-del	-/T			intron-variant	NEB	GRCh38.p7	2:151671530	GTTTATCTTAAAGCA[-/T]TTTTTTTCAAGTCAC	4703
rs576645878	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151554281	TAGAAAATGTTCAGG[C/T]TGGGCATGATAACTC	4703
rs576660293	snp	A/G	0.000399281	0.0141238	synonymous-codon	NEB	GRCh38.p7	2:151540353	GCATACATCACTGGC[A/G]TTCCAGTAAGCCCTC	4703
rs576670286	in-del	-/T	0.0023933	0.0345097	intron-variant	NEB, RIF1	GRCh38.p7	2:151504231	GTACCCAGATTTTAA[-/T]TCTTAAAATCAGTGA	4703
rs576696191	snp	C/T	3.11095e-05	0.00394383	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151490430	GTGGTGGTCTGGTGC[C/T]TCTGAATGCTCAGAC	4703
rs576710510	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151554856	ATGATGTTAGCACAA[A/C]AATGAAATCACATAA	4703
rs576729161	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151605230	AATCATTGACTGGTG[A/G]CAATTATGATCACAG	4703
rs576759199	snp	A/C			intron-variant	NEB, RIF1	GRCh38.p7	2:151502224	GGACTTGCAGGAAAG[A/C]GTGGAAGTGAGGCGA	4703
rs576784287	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151684023	GGGTTAGTCAAACTT[A/T]GAAACAAAGCGTAGA	4703
rs576839373	snp	G/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151510242	TGGAGGCCTGGGGAG[G/T]TTTTTTTAGACCCAC	4703
rs576892246	snp	C/T	0	0	intron-variant	NEB	GRCh38.p7	2:151649527	TTTCAGGGCACATAC[C/T]TCAGTATTCTGTAAT	4703
rs576901009	snp	A/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151509618	AGGAAGAGAGGTTTT[A/T]TTTTTGTTTGTTTGG	4703
rs576914148	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151576063	GTTATTAATAAAGTT[C/T]TTATTATTCTAAAAT	4703
rs576918934	snp	C/T	0.0134222	0.0808143	missense, intron-variant	NEB	GRCh38.p7	2:151604849	TGGCCCAGTTGCTTA[C/T]GGTAACCTTCTTTGT	4703
rs576940894	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151518478	CTGCTCAGCATTCCT[A/G]TTTTTCCTCTTTAGA	4703
rs576956539	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151642242	GCATAGGTTGGGTTT[G/T]GAAGGAACCCTACAA	4703
rs576961127	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151621368	CTCCAAATTTGAATT[A/G]GGAACATTTTTACTA	4703
rs576962825	snp	A/C	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151676697	TCTCACTTGCCTGGG[A/C]AACTCTGGTAGGCAG	4703
rs576979783	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151540519	CCAAGCCACCTACAG[A/G]TCTTGTGGAGGGGCA	4703
rs577022318	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151676149	ATGTAAACTGGTATG[C/T]ATGTACCCAAGATAA	4703
rs577031998	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151628473	TTTGTTGTTGGTGGT[A/G]GTAAGGGCAAACTGG	4703
rs577037083	snp	C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151526352	AGTAGAACAGCAGCG[C/T]TGACAATACTAAACT	4703
rs577066629	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151539651	ACCCGTAAGGATTGG[C/T]TATTTACCTTGGATT	4703
rs577091219	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151668873	CAAAATTTTATTGCC[A/G]CCCCCTAGGCTCATG	4703
rs577111489	snp	C/T	0.00159617	0.0282053	intron-variant	NEB, RIF1	GRCh38.p7	2:151505791	CTCGTCTCTTTGGGG[C/T]AGGGATGGGGGCCCC	4703
rs577125380	snp	A/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151512586	CCCAAAGTGCTGGGA[A/T]TACAGACGTGAGCCA	4703
rs577134008	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151547087	GAGGTCAGAGTAGGG[A/T]TGAGTGAGAGGAAAA	4703
rs577162274	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151674733	AAGTGTCACACTGTG[C/T]GTAGCATGAGATCAT	4703
rs577168374	snp	A/G	0.00199481	0.0315187	intron-variant	NEB, RIF1	GRCh38.p7	2:151503643	ACTACTTTGAAAACT[A/G]GGCACTAAATTATGC	4703
rs577188214	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151613512	CCATTGTAAGTATAA[A/G]CAATATATTACAGCA	4703
rs577213817	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151635567	CAAAAAATTATGGGC[A/G]TGGTGGTGAGTGCCT	4703
rs577229428	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151507206	ATTTTAAAAAACATA[C/T]AAAGCTAGGGGTTTG	4703
rs577236124	in-del	-/T	0.00318978	0.0398085	intron-variant	NEB	GRCh38.p7	2:151706076	GACTGAAATAAAATG[-/T]TTTTTTAAAAGAAAG	4703
rs577252319	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151665162	ATGATCTGAGGGGTC[A/G]CTATGAAAGAGAACG	4703
rs577263334	snp	A/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151726098	AATGATAATGTGCAT[A/T]ATTTATCATTATAAA	4703
rs577263890	snp	C/T	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151732790	TTTTCAGAACTTTCT[C/T]TTCGTCTCTGTCCCT	4703
rs577274382	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151633506	CTATTAGTGTATTCA[C/T]AATAAAGCAATAAAA	4703
rs577289601	snp	A/C	0.000399281	0.0141238	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151506638	ATGTCAAAAAGAAAT[A/C]CATCTTCTTGGAGCA	4703
rs577300387	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151619179	ATTTTTAAGGGCTAA[A/G]TTTCATCTGATTCAA	4703
rs577314666	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151532977	TCAAAGTCAAGAGGC[A/G]CCATGAATATATACA	4703
rs577322365	snp	C/T	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151637616	CCTGGGACTGGCAGC[C/T]GAGTAGCCGCACTAA	4703
rs577326703	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151509491	CATTTGCACACAGAA[C/T]TTGGATGTATTCTGG	4703
rs577335449	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151704853	CTGGGAGCTGTAGAC[C/T]GGAGCTGTTCCTATT	4703
rs577347137	in-del	-/GAA	0.00358779	0.0422022	intron-variant	NEB	GRCh38.p7	2:151723084	CTCATGCTCTAATGG[-/GAA]GAATACTAGTCTTGG	4703
rs577350705	snp	A/G	5.15743e-05	0.00507784	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151492388	AATTCCTGACTCACC[A/G]TTGAGATGTGCCGTT	4703
rs577351442	snp	C/T	0.0142736	0.0832652	intron-variant	NEB	GRCh38.p7	2:151595408	AGGCTCCCGCCACCA[C/T]GCCCAGCTAAGTTTT	4703
rs577370516	snp	C/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151496712	ACAAACGGAAAAACT[C/G]ATTTTTAAAAAATGA	4703
rs577374558	snp	G/T	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151705393	CAACAAAGGAGATTT[G/T]AACTTGGGCTTTTAG	4703
rs577380338	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151535543	TGTTGGATGGTGACA[C/T]TATAGAGTCTTTTCC	4703
rs577381350	in-del	-/AAAA	0.566701	0.118995	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151498891	CAATGATAAGGTGCT[-/AAAA]AAAAAAAAGAAACTT	4703
rs577399266	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151610356	ATAATGCCAAAATGT[A/G]TTTTTATTCTCTGTA	4703
rs577407348	snp	A/G	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151561457	TTCTAGAGTCCTGCA[A/G]ACTTTGTATGGCTGC	4703
rs577410545	snp	A/G	0.000298364	0.0122104	missense	NEB	GRCh38.p7	2:151655906	TGCTCGGGTGCTGGC[A/G]GTATTTCTGATCACT	4703
rs577431684	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151692831	AAAAATTAGCCGGGC[A/G]TGATGGCACATGTCT	4703
rs577447763	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151618176	TTTAAGAAGGTATCA[C/T]AATGCTTATTATTAT	4703
rs577448257	snp	C/T	1.66524e-05	0.00288547	intron-variant	NEB	GRCh38.p7	2:151725436	TCCCTCTCCTTTATT[C/T]CAGCAATGCAGCCCA	4703
rs577482758	snp	C/T	1.65919e-05	0.00288022	intron-variant	NEB	GRCh38.p7	2:151554914	CTAGTCATTAAGGGG[C/T]GCATGACCGTACTTA	4703
rs577494262	snp	C/T	6.63383e-05	0.00575888	synonymous-codon, intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151534317	ATCAGCTCTGTATTT[C/T]TTCTGCTCAAACATC	4703
rs577514019	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151716028	TTTAAAAATAGATTC[A/C]TTTTTCTTTCTAAAT	4703
rs577518808	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151551270	CACCGCACCTGGCCA[A/G]AAATTATTTTTAATA	4703
rs577525536	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151659502	GATGGGTTTTTGCCA[C/T]GTTGCCCAGGCTGGT	4703
rs577535881	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151722590	TCGCTGTTGCCCAGG[C/T]TGGAGTGCAGTGGCT	4703
rs577558302	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151624844	GCTATTTATGCAGCA[A/G]TATTTCTGGACTGCA	4703
rs577563614	snp	A/T	0.00318978	0.0398085	intron-variant	NEB	GRCh38.p7	2:151672061	TTTGTATCTATCACC[A/T]TTGCAGCCAACCCAT	4703
rs577564071	snp	A/C	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151500244	GAAAGTTACTGATCT[A/C]ATTATGTCAAAGAAT	4703
rs577565427	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151611745	TAATGTGGAGGAGCA[A/C]CCTGAGCAACCAATT	4703
rs577567436	in-del	-/A	0.00597247	0.0543191	intron-variant	NEB	GRCh38.p7	2:151636624	ATCTCTACTAAATAT[-/A]AAAAAAATTAGCTGG	4703
rs577573338	snp	A/G	1.65696e-05	0.00287828	missense, intron-variant	NEB	GRCh38.p7	2:151619614	GGGCTGCTGTACCTT[A/G]TCTTGTATTTCTCAA	4703
rs577576908	snp	C/T	0.000399281	0.0141238	downstream-variant-500B, intron-variant	NEB, RIF1	GRCh38.p7	2:151485080	GCCTTTGCCACATGC[C/T]GCCATCCTACTGGAT	4703
rs577598374	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151623644	TTATAGTCTTTTCAA[A/G]ATGAGATTTTATAAG	4703
rs577600012	snp	C/T	1.65611e-05	0.00287755	missense	NEB	GRCh38.p7	2:151672514	ATGCTAACCATGTCC[C/T]CAGGGGTATGGTAGC	4703
rs577627895	in-del	-/C	0.00362318	0.0424083	intron-variant	NEB	GRCh38.p7	2:151551521	AACTTGTAAATATTG[-/C]TAAAACATGCCCATT	4703
rs577630679	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151615053	TTTAGATAGAGTTTA[C/T]GTGTCACCAGGAAAT	4703
rs577630811	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151606370	TAATACAGACTCTTC[A/G]TGATGTTTTGTTTCT	4703
rs577635321	snp	C/T	3.72946e-05	0.00431809	intron-variant	NEB	GRCh38.p7	2:151630711	CACAGATTTTTGCTC[C/T]TACCTCACTGTAGTT	4703
rs577654358	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151559417	AACTAGAAATACCAT[C/T]TGACCCAGCAATCCC	4703
rs577666634	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151572859	CCAGCCAAGTATGTA[A/T]ATATTTTTAACTAAA	4703
rs577666822	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151630120	GTTTAAAAGACAAAT[A/G]AGAAAAATTAAAATA	4703
rs577667600	snp	G/T	1.73285e-05	0.00294346	intron-variant	NEB	GRCh38.p7	2:151614231	GGCACAAAAGAGTTA[G/T]AATGCTTTTCTAAAC	4703
rs577676687	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151679036	CAGCAAGAGGAGACC[C/T]GCAGGAGGAGGGCGC	4703
rs577701098	snp	A/G	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151616407	AAAAAATTATTTACT[A/G]GCCGGGCGTGGTGGC	4703
rs577702109	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151519577	TTGTGAGTGTTATAA[A/G]TGCTACTGAATTGCA	4703
rs577705900	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151655556	AAAAAAATCTTTTAA[A/G]TATTTTCTATTTTCT	4703
rs577719000	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151689275	AGTGACACAATCTCG[G/T]CTCACTGCAACCTCC	4703
rs577730451	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151569669	TGGGAAATCCGACAT[C/T]TGTACACAAAAATTT	4703
rs577744452	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151579194	AACTTTCTGAAGAAA[A/C]CTGGCTGTAGGTAGG	4703
rs577751355	snp	C/T	0.00438332	0.0466095	intron-variant	NEB	GRCh38.p7	2:151702174	CATGTAGTTGAGCGG[C/T]TTTGAGTGAGATTCT	4703
rs577781118	snp	C/T	0.0252325	0.109451	intron-variant	NEB	GRCh38.p7	2:151702694	GGATTGCAACCCCTG[C/T]CTTTTTTTTGTTTTC	4703
rs577787000	snp	A/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151494338	TACAGATAACTTTTG[A/T]TTATCTTTAGGGCCC	4703
rs577792197	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151631463	CGTAGAAAACAAGCG[C/T]GTTGTATAAGGCAAA	4703
rs577792311	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151623006	GGCATTCTTGGGCAG[A/C]TAATTTAGAAGAGTG	4703
rs577807450	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151513482	TGCCATTGTATGCAT[A/G]TGACTGTCACCAATA	4703
rs577815440	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151640195	CACACAATATTCCTC[C/T]TTGGTCTGAAGGGTT	4703
rs577818221	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151653104	AGATTCCATTTTTAG[A/G]CATTCCTTTCCTGCA	4703
rs577839043	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151564978	TGACAAAATCAGCCA[A/T]GAATATGAATGCAAC	4703
rs577843590	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151722291	CATGTAAGAAAGTAC[C/T]TCAAAATAAGGGAGA	4703
rs577856870	snp	C/T	8.28851e-05	0.00643705	missense, intron-variant	NEB	GRCh38.p7	2:151644563	GCTCCTCATAACCCA[C/T]TCGGTAGAGTTTCTG	4703
rs577871503	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151730064	ACTCACTGTTTGCAA[A/C]CTAACAATAAACTAA	4703
rs577874679	snp	A/G	0.00083043	0.0203599	intron-variant	NEB	GRCh38.p7	2:151551857	CAGCCTGGTGCAGAA[A/G]GAAGCATTGTTAGAA	4703
rs577883889	snp	A/T	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151543270	AAATTCTAATCATGG[A/T]TATAAATACCAGTTG	4703
rs577894144	snp	C/T	0.000314577	0.0125375	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151643899	CTGGTGCAGGTAGTT[C/T]TTGTAGTCCACGTCG	4703
rs577895344	in-del	-/A	0.0302959	0.11929	intron-variant	NEB, RIF1	GRCh38.p7	2:151488653	CTGTCTCTAAAAATA[-/A]AAAAAAAAGTATTCT	4703
rs577919574	snp	C/T	0.00199481	0.0315187	intron-variant	NEB, RIF1	GRCh38.p7	2:151492560	TCAAAGCCTTTCCAG[C/T]AGATAGAGATGGATA	4703
rs577939684	snp	A/C	3.31279e-05	0.00406975	missense	NEB	GRCh38.p7	2:151697430	AATGTCCCAAAATAT[A/C]TTTTAAGTAGGAATC	4703
rs577964703	in-del	-/G	0.15698	0.23205	intron-variant	NEB	GRCh38.p7	2:151579760	TTTTTTGGGGGGGTC[-/G]GGGAATACTGTTTTT	4703
rs577965267	snp	C/T	0.0217236	0.101931	intron-variant	NEB	GRCh38.p7	2:151664245	GATTGCATCTTTACA[C/T]TTGCTTAGGATTGTA	4703
rs577984867	snp	A/G	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151697849	AGGCGGGCGGATCAC[A/G]AGGTCAGGAGTTTGA	4703
rs577986799	snp	G/T			upstream-variant-2KB	NEB	GRCh38.p7	2:151735624	GTAATCTCGCTGGGC[G/T]TGGTGGCTCACGCCT	4703
rs577996029	snp	A/G/T	3.32497e-05	0.00407722	intron-variant	NEB	GRCh38.p7	2:151650382	ATTTATATAGATTCT[A/G/T]TGAAAAGACAGAGCA	4703
rs578023308	snp	C/T	0.000248585	0.0111459	missense	NEB	GRCh38.p7	2:151656323	GGTAGCTGGTCTTTG[C/T]GTTCTCATAGTTTTT	4703
rs578039411	snp	A/C			missense, intron-variant	NEB	GRCh38.p7	2:151625584	TGATTTCAGGTGTAT[A/C]AGGCATAATATGGAC	4703
rs578058542	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151549351	GCATCTGTGCTAAGT[A/G]AGGCCAGCAGAAGTA	4703
rs578076414	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151498423	CCTGCTTTGGAGCAG[C/T]TGGGAGTGGGAAGGG	4703
rs578076971	snp	A/C	0.00517822	0.0506191	intron-variant	NEB	GRCh38.p7	2:151702451	TCGTTGATCTGTCTA[A/C]TGTTGACAGTGGGGT	4703
rs578091424	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151572147	GCCAACATGGTGAAA[A/C]CTTGTCTCTATTAAA	4703
rs578101732	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151532621	GTTCAGGCAAACAGG[A/G]TATTTATAGGAGGAG	4703
rs578122962	snp	C/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151695996	CACTGTCAGTGCTCA[C/T]GTACCAGAGCCACTT	4703
rs578124296	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151571085	ATCTCGGCTCACCCC[A/G]AACTCTGCCTCCCAG	4703
rs578126100	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151664035	CATTTTTTTTTTTCC[C/T]GAGACTTGAGTCCAT	4703
rs578126381	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151541306	AAAAGAGAACTGCTT[A/C]TTCAAGTGCAGTGTT	4703
rs578172403	snp	G/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151527367	CTCCTCTCCTTCTCG[G/T]ATCTCAAACGAGCAA	4703
rs578183119	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151633252	CAGAGACTTCTTTTA[C/T]TTCATAAGCATAATA	4703
rs578185837	snp	G/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151651359	TATTCTTATGGAAAT[G/T]ATAATCCTTACGGGC	4703
rs578199142	snp	C/T	7.13521e-05	0.00597252	intron-variant	NEB	GRCh38.p7	2:151563945	TCTAGAACAAAGAAA[C/T]ACATGGCAACAAAAG	4703
rs578211653	snp	A/C	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151685142	CCATTGAAATTCCCC[A/C]AAAAAGCACGCATGG	4703
rs578220161	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151630606	TTGGATGAGTGGAGT[A/G]TTAAATGAAAGAGCC	4703
rs578224884	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151577953	CCTGGCACATGGTGT[A/G]TTTAATAAGTATTTT	4703
rs578229327	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151685730	TGCTAGTTGGGTCAA[A/G]TTCCCAGCTTCATTG	4703
rs578251637	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151533306	GAGATCATTTACAAG[A/G]AATGAATATTTACAT	4703
rs587780397	in-del	CTTAT/GAG			frameshift-variant	NEB	GRCh38.p7	2:151553413	TCCATGCCAAGCATG[CTTAT/GAG]GATCTACGTGATGAT	4703
rs587780398	snp	A/G	1.66192e-05	0.00288259	NEB	2	allele_origin=G(germline)/A(germline)	2:151727741	GATCCTTCAAAGTTC[A/G]TGACCCCCTACATTG	4703
rs587780399	snp	A/G			splice-donor-variant	NEB	GRCh38.p7	2:151677875	CAGATACAGAGTGAT[A/G]TAAGTGTCATTTACT	4703
rs727504032	snp	C/G			missense	NEB	GRCh38.p7	2:151568664	CGCCTGTGGATGACA[C/G]AGTTGATTATGTGAC	4703
rs727504033	snp	C/T	8.2837e-05	0.00643519	NEB	2	allele_origin=T(germline)/C(germline)	2:151627116	GTGCAAGAGAGCTGC[C/T]GAAATACTGAGTGAT	4703
rs727504034	snp	A/G	8.28301e-05	0.00643492	NEB	2	allele_origin=G(germline)/A(germline)	2:151627118	AAGTGCAAGAGAGCT[A/G]CTGAAATACTGAGTG	4703
rs727504035	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151629535	GTTATCAGTGATGTG[A/G]GTAGCAACACCCTAG	4703
rs727504036	snp	A/G/T	1.6582e-05	0.00287936	NEB	2	allele_origin=T(germline)/A(germline)	2:151677982	CTAAGAAAGCCCAGG[A/G/T]TGTGGTCAGCAATGT	4703
rs727504037	snp	A/G	3.32198e-05	0.00407539	NEB	2	allele_origin=G(germline)/A(germline)	2:151727767	GGAGGAAGGTCATCC[A/G]GAAGAAAGTGGATCC	4703
rs745307272	snp	A/C			utr-variant-3-prime, intron-variant	NEB, RIF1	GRCh38.p7	2:151485436	CATTAGCAATCAGCA[A/C]GGAAAAGGTGAACAT	4703
rs745308961	snp	A/G	8.61527e-05	0.00656269	intron-variant	NEB, RIF1	GRCh38.p7	2:151503483	AAAGGTAAAATGACC[A/G]TAAATCCTTTAGATA	4703
rs745315104	snp	C/T	1.66532e-05	0.00288554	intron-variant	NEB	GRCh38.p7	2:151568271	CAGTTCCATTAAGGC[C/T]CTCCACTCGTACACA	4703
rs745320297	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151658441	CATCAAAAGAAAACA[C/T]CTCTGTTTTAGAATC	4703
rs745323298	snp	A/C/G/T	0.000104834	0.0072393	missense	NEB	GRCh38.p7	2:151658075	TAGACTCTTCCAAGG[A/C/G/T]AAGTTTGTAGAGTTT	4703
rs745325085	snp	A/G	3.32187e-05	0.00407532	synonymous-codon	NEB	GRCh38.p7	2:151727772	CACTTTCTTCCGGAT[A/G]ACCTTCCTCCTCTCC	4703
rs745335695	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151690461	GTTTTAGTGTGCATG[C/T]GACAGATCCTAATGA	4703
rs745338464	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151709600	ACAAGAGCCAAAGTT[A/G]TAAGAAATTTACCCA	4703
rs745348500	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151641409	CAATCATGTCTCACT[A/G]CAACCTCCAACTCTT	4703
rs745349330	snp	C/T	1.65883e-05	0.00287991	intron-variant	NEB	GRCh38.p7	2:151695718	ATTAGTTCAGAAGAA[C/T]TGTTCCAGAATACAA	4703
rs745358590	snp	C/T	1.69654e-05	0.00291246	missense, intron-variant	NEB	GRCh38.p7	2:151610101	CCTTTCTGTTTCTCA[C/T]AGGCTTCCTTGTATT	4703
rs745359696	in-del	-/AGTA	0.000486204	0.0155841	intron-variant	NEB, RIF1	GRCh38.p7	2:151496242	GTAGTTTTTAAAATC[-/AGTA]AGTAAGTAGTTTTTT	4703
rs745360846	snp	C/T	1.66175e-05	0.00288244	intron-variant	NEB	GRCh38.p7	2:151554881	ACATAACGAGCGGCA[C/T]ATTTCTCAGAATGTA	4703
rs745363472	in-del	-/AA			intron-variant	NEB, RIF1	GRCh38.p7	2:151500565	TGGCTTGTTTTGAAT[-/AA]AAGTATCAAAATAAG	4703
rs745382279	snp	C/T	3.31505e-05	0.00407113	missense	NEB	GRCh38.p7	2:151671136	TCTCATTTAATGCAT[C/T]GCCTGCTTTCTTGAC	4703
rs745386853	snp	C/G	7.4758e-05	0.00611338	intron-variant	NEB	GRCh38.p7	2:151675416	AATGCATTTCACATA[C/G]TGCAAAAAGGAAAAT	4703
rs745386924	snp	C/G	1.66749e-05	0.00288741	intron-variant	NEB	GRCh38.p7	2:151680699	TGTATTAGTTAACAT[C/G]TATTAACATATAGAT	4703
rs745401996	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151638479	TCTCCATCTCTGGGG[G/T]TTGGCACAGATTTGT	4703
rs745404405	snp	C/G	2.92916e-05	0.00382687	intron-variant	NEB, RIF1	GRCh38.p7	2:151531746	CCCTCCATGTTTGCA[C/G]ATGCCCCCTGAGTTT	4703
rs745410848	snp	A/G			synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151643857	CCGAGCATGGATGAC[A/G]TCGCTCTGGTCGGGC	4703
rs745413093	snp	A/C/T	8.51222e-05	0.0065234	intron-variant	NEB	GRCh38.p7	2:151663887	AAGAAATTATGGTGA[A/C/T]GAAAATGGTAAAAGA	4703
rs745415126	snp	A/G	8.65239e-05	0.00657681	intron-variant	NEB	GRCh38.p7	2:151540474	AATGCAGAAGAGAGA[A/G]ACAAGCTTAAGTGTC	4703
rs745420110	snp	A/T	1.70287e-05	0.00291788	stop-gained, intron-variant	NEB	GRCh38.p7	2:151643344	ACTGAAGGTCTGACT[A/T]GTACAAATTCTGAAA	4703
rs745425031	snp	A/G	1.65605e-05	0.0028775	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151514366	TAGCATGTCAGGTGT[A/G]TCTTCCATTTCAGTG	4703
rs745427052	snp	A/G	1.65669e-05	0.00287805	intron-variant	NEB	GRCh38.p7	2:151575669	GTAACTTTCCAAACA[A/G]AAAGAGAGTCTGTTG	4703
rs745435880	snp	A/C	1.66369e-05	0.00288412	intron-variant	NEB	GRCh38.p7	2:151625491	TCCTACATCGGCAAC[A/C]ATCAATGTGGCCAGA	4703
rs745437510	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151486251	AGCACACAAAAGGAT[A/G]CTCAAAATTAGTCAT	4703
rs745444923	snp	C/T	1.65652e-05	0.0028779	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151485870	TTATGATGGCATCTC[C/T]ATCCTTGAAGGACAC	4703
rs745445273	snp	A/C	3.31455e-05	0.00407083	missense, intron-variant	NEB	GRCh38.p7	2:151631313	GGACCCAGCCAATGC[A/C]TCTCAGCCACTGGAG	4703
rs745448583	snp	A/G			synonymous-codon	NEB	GRCh38.p7	2:151563883	GTAGCGCTCATCCAG[A/G]GTGTAGCCATAGGCC	4703
rs745449733	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151517055	TTTATAAGTAAACAA[C/T]TCTATGTGGGTCCTG	4703
rs745456462	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151679209	GAGCAAAATGACTTC[A/G]GTTCACATCTTGGTT	4703
rs745458642	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151712627	TGACACAGGAGGAGG[C/T]TGGAGCTTGCTGGCT	4703
rs745481666	snp	C/G/T	3.57113e-05	0.00422547	synonymous-codon	NEB	GRCh38.p7	2:151684832	ATTGATGCTATCAGG[C/G/T]GGGTAGCTGTAACTG	4703
rs745481978	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151644909	AATCCTAGATGGTAC[A/G]GCCTAGTACACACCT	4703
rs745483038	snp	A/C	4.97814e-05	0.00498881	intron-variant	NEB	GRCh38.p7	2:151692025	CTCTCAAACAATGTC[A/C]CTGTGAGGCATGAAC	4703
rs745485126	in-del	-/AA	0.00362829	0.042438	intron-variant	NEB	GRCh38.p7	2:151639263	CAGTGTGCAAATGTC[-/AA]AGAATCTGCTCTCAC	4703
rs745488953	snp	A/T	6.65657e-05	0.00576875	intron-variant	NEB	GRCh38.p7	2:151644438	GATAAATTGCAATCA[A/T]ATCAATATCAACAGA	4703
rs745490728	snp	C/T	3.84978e-05	0.00438719	intron-variant	NEB	GRCh38.p7	2:151655259	TAAAATTAATTTTTA[C/T]ATAAATTTACCTGAC	4703
rs745503224	snp	C/T	1.66582e-05	0.00288597	synonymous-codon	NEB	GRCh38.p7	2:151717482	AGCCAGAGGCGTGAA[C/T]TGAGCTTGCTGTTCA	4703
rs745504838	snp	C/T	1.65658e-05	0.00287795	missense, intron-variant	NEB	GRCh38.p7	2:151610580	TCTGCTCTCAGATCA[C/T]AGTCCTTCATCTTTG	4703
rs745511810	snp	C/T	1.65897e-05	0.00288003	splice-acceptor-variant, intron-variant	NEB, RIF1	GRCh38.p7	2:151518423	CTTCTTGTACTGGTA[C/T]TGAGGGGAAGGCGGC	4703
rs745517888	snp	C/G	1.65614e-05	0.00287757	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151526039	TGAGCCCTGTGCCAA[C/G]TGCTTCTTGACATGG	4703
rs745520362	snp	G/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151518093	CACACTCTTTATGCT[G/T]CCAGCCCCTGCCAGT	4703
rs745524418	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151715960	CATATTTAAATAAGG[C/G]AAAAGAATGTTTCCT	4703
rs745529494	snp	A/C			intron-variant	NEB, RIF1	GRCh38.p7	2:151505266	GACAGGTAGGAAAAG[A/C]AAGCCAAATCCCTTC	4703
rs745532672	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151551343	ACCATTGGGTAACAT[A/G]GAATAGGTAGGTTAA	4703
rs745534711	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151734098	AGGAACGTAGAGCAG[C/G]GTATCTTCTTTTTCA	4703
rs745539800	snp	C/T	1.65671e-05	0.00287807	missense	NEB	GRCh38.p7	2:151568348	CAGCCTCCTGGGCAG[C/T]GTGCAGCAGGGGGGT	4703
rs745553889	snp	A/T	3.39311e-05	0.00411879	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151494243	TTCCCCACATTTTCT[A/T]TGTACAAAACCTATG	4703
rs745555630	snp	C/T	1.65644e-05	0.00287783	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151631266	TATTTCGGTAGCTCT[C/T]TTGCACTTGACCACA	4703
rs745561094	snp	G/T	1.68244e-05	0.00290033	missense	NEB	GRCh38.p7	2:151671195	ATCCATCCGATGCCC[G/T]TCAAGAAGCTGTTAT	4703
rs745573198	snp	A/C	1.65608e-05	0.00287752	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151525966	CACTTACATCACTGA[A/C]ATGCTTGGTCACTTC	4703
rs745573366	snp	A/G	1.6577e-05	0.00287893	synonymous-codon	NEB	GRCh38.p7	2:151659065	GGGAACTATACTTAC[A/G]TCACTCATATTAATT	4703
rs745579334	snp	C/T			missense, intron-variant	NEB	GRCh38.p7	2:151617374	CTTACATCACTGTAG[C/T]TTATTCGGTTGAGTT	4703
rs745581012	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151631898	ATTCTTATTCCCTGC[A/G]ATGTATTCTTCTATA	4703
rs745586435	snp	C/T	1.84252e-05	0.00303517	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151531848	CTGGAGTATCCACAA[C/T]TGAGGTAAATTTGTC	4703
rs745593343	snp	C/T	1.80853e-05	0.00300705	intron-variant	NEB	GRCh38.p7	2:151663512	TGGTTGCTTATTATC[C/T]AGAGTAAACGCTCTG	4703
rs745600430	in-del	-/ATGTCCA	1.69971e-05	0.00291518	frameshift-variant, intron-variant	NEB	GRCh38.p7	2:151650633	TCTGATCAGGCAGAC[-/ATGTCCA]CTGATGCAGGTAGTT	4703
rs745615279	snp	C/T			missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151492472	CCTTGTATTTGTTTC[C/T]GGAAACTATCAGAAT	4703
rs745615339	snp	C/T	6.62636e-05	0.00575564	missense, intron-variant	NEB	GRCh38.p7	2:151644536	CAGGAAGATCGTAAC[C/T]TTTTCTCTTCAGCTC	4703
rs745617522	snp	A/G			intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151506571	ACAAAATCCATTAAA[A/G]AAATGCAAACTCAGT	4703
rs745620924	snp	A/G	1.67615e-05	0.0028949	synonymous-codon	NEB	GRCh38.p7	2:151666108	ACTCTGAATCTGCAT[A/G]GCATTCCTGGAGTGC	4703
rs745632829	snp	A/G	4.8846e-05	0.00494172	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151491770	TAGTACGCCAGACAC[A/G]TAAACCTGAAAGGGA	4703
rs745639468	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151716929	TTTACTGCCTAAATA[C/T]AGGTAGACTAAGCTG	4703
rs745641069	snp	A/T	1.92937e-05	0.00310587	missense	NEB	GRCh38.p7	2:151561092	TTAATCTGATGATAA[A/T]TTTCTTTATATTTTA	4703
rs745641419	snp	A/C	1.65594e-05	0.0028774	missense, intron-variant	NEB	GRCh38.p7	2:151627651	ACTTCTTGGCTAACA[A/C]CACTCCCAGCATGTC	4703
rs745645792	snp	A/G	1.94339e-05	0.00311714	intron-variant	NEB	GRCh38.p7	2:151679682	AGCCCACCCACCCAC[A/G]TTTTCTAGTTGCCCA	4703
rs745648379	snp	A/G	5.42079e-05	0.00520586	intron-variant	NEB	GRCh38.p7	2:151565165	TAAGGAGAGAAAACC[A/G]AATCTTTTATTACTA	4703
rs745662866	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151729055	ATAAAGCATGAGAGA[A/G]GTATTTCACCTTGAA	4703
rs745668945	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151618824	CACACTGAGACTGAT[G/T]GTGCGTGAGTACTGC	4703
rs745671713	snp	C/T	1.74066e-05	0.00295008	intron-variant	NEB	GRCh38.p7	2:151546044	AGTTGATTAATCATT[C/T]AAGGGATTCATGTCA	4703
rs745678940	snp	A/G	3.62332e-05	0.00425621	intron-variant	NEB	GRCh38.p7	2:151537106	ATGTCGAATGGATGA[A/G]GCCAATTCTCCTTGA	4703
rs745679694	in-del	-/AGA	2.83974e-05	0.00376801	intron-variant	NEB, RIF1	GRCh38.p7	2:151530946	TTGTTACATCTCATT[-/AGA]AGGAGGCCAAGATGA	4703
rs745684008	snp	C/T	4.02423e-05	0.00448548	intron-variant	NEB	GRCh38.p7	2:151665545	TGTACAGATTCTTTA[C/T]AATGAGAAAAAAAAT	4703
rs745689055	in-del	-/A			intron-variant	NEB	GRCh38.p7	2:151681607	AAATGGTTTTCATCG[-/A]AAACAAAACACCGAA	4703
rs745689099	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151651861	ATTGCTTTTTAAAAA[C/G]CAGTGCCATAGATTT	4703
rs745697868	in-del	-/AG			intron-variant	NEB	GRCh38.p7	2:151570682	TGGAATTAATACCAC[-/AG]GGGCACAGTTTTGAA	4703
rs745706462	snp	A/G	1.656e-05	0.00287745	missense, intron-variant	NEB	GRCh38.p7	2:151627584	TGGTCGGGCAGGCAC[A/G]TCCACTCGTGCAGGT	4703
rs745710574	snp	C/T	2.08984e-05	0.00323246	intron-variant	NEB	GRCh38.p7	2:151610730	CATTTTAATTAATCT[C/T]AGGTTTAAGCAACAA	4703
rs745718073	snp	C/T			missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151525261	CCTTGACAAACTTCT[C/T]TTTGTAATTTGTCTA	4703
rs745727353	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151705390	TATCAACAAAGGAGA[C/T]TTGAACTTGGGCTTT	4703
rs745733944	snp	A/C	1.65611e-05	0.00287755	missense	NEB	GRCh38.p7	2:151694402	ACTCCAATCATTTTC[A/C]CTTTGTTTTTTTCAT	4703
rs745748427	snp	A/G	1.65685e-05	0.00287819	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151619580	CTTCTTGGCCAAAAC[A/G]ATACCAAGCATGTCC	4703
rs745763058	snp	C/G	1.81549e-05	0.00301283	intron-variant	NEB	GRCh38.p7	2:151547609	CCTAGTCTCTACTCC[C/G]TGTCTTTCCTAAGAA	4703
rs745770468	snp	C/G	1.67744e-05	0.00289602	intron-variant	NEB	GRCh38.p7	2:151553515	AATCTAGAGGGTTTT[C/G]ATAGAAAGGATCAGA	4703
rs745772328	snp	A/C	6.68952e-05	0.005783	intron-variant	NEB	GRCh38.p7	2:151674465	TAAACTTCACCTAAA[A/C]TTTGTACTCACATCA	4703
rs745773397	snp	C/T	1.6577e-05	0.00287893	missense	NEB	GRCh38.p7	2:151656266	TGATGTTGGCTTGGG[C/T]ATCCTTTGCAGCCGT	4703
rs745778403	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151573531	AGAGAAAATACATCA[A/G]CGCCCTAAAATTATA	4703
rs745779078	snp	C/T	6.63691e-05	0.00576022	missense, intron-variant	NEB	GRCh38.p7	2:151614301	AGGTCATAGGCCTTC[C/T]GAGCCTGAATGACGT	4703
rs745784289	snp	C/T	1.87929e-05	0.00306531	intron-variant	NEB	GRCh38.p7	2:151642714	AGTAAGTTGGATTTA[C/T]AAAGTGCATTGTAAG	4703
rs745791097	snp	C/T	0.000141894	0.00842182	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151527564	GGGCTTTGTTGGCTT[C/T]GTACTGTTTCTTATA	4703
rs745794482	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151706154	CATTTATACCCTCTC[A/C]CTTGCCACTTTCCCA	4703
rs745794892	snp	A/T	3.51185e-05	0.00419023	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151512738	ATGTCCTTACCTGGC[A/T]TGAAAGATTCTTGAC	4703
rs745801833	snp	A/T	1.71272e-05	0.00292632	intron-variant	NEB	GRCh38.p7	2:151724985	ATAATGCACAGTTAG[A/T]GTTCATGACAGGCAT	4703
rs745811089	snp	A/T	1.70731e-05	0.00292169	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151636281	GGGGATGGCGTCGCT[A/T]CGCAAGTCATAGCCT	4703
rs745836611	snp	A/G	1.70313e-05	0.00291811	missense	NEB	GRCh38.p7	2:151570214	TTAGAGTGCAGGATG[A/G]AAAGCATGTCCACAG	4703
rs745843859	snp	A/C	1.65647e-05	0.00287786	missense	NEB	GRCh38.p7	2:151694344	CTGGTTTTTGGCCAC[A/C]TTCAAGGAGTGCAGC	4703
rs745856699	in-del	-/ATTT			intron-variant	NEB, RIF1	GRCh38.p7	2:151489941	CAAAAATTAAGAATA[-/ATTT]ATTTAAGTGAGTTGT	4703
rs745870274	in-del	-/G			intron-variant	NEB	GRCh38.p7	2:151686981	TGGAGTCTTTTTCTT[-/G]GATCTAGACCAAACT	4703
rs745875222	snp	A/G	1.74818e-05	0.00295645	intron-variant	NEB	GRCh38.p7	2:151665320	TGGGCGAGGCTGGCA[A/G]GTGAGTCCTTACCTT	4703
rs745881254	snp	A/G	0.000104064	0.00721256	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151610112	CTCATAGGCTTCCTT[A/G]TATTTGTACTAAAAT	4703
rs745882588	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151629213	CCTCTTTTGCCATTT[G/T]CTATTTTCTGTGAGG	4703
rs745887781	in-del	-/T			intron-variant	NEB	GRCh38.p7	2:151626114	AGATTTGCATCTTTC[-/T]TTTTTTTTTTTTTTT	4703
rs745891821	snp	A/G			synonymous-codon	NEB	GRCh38.p7	2:151672528	CCCAGGGGTATGGTA[A/G]CTGGTTTTGGTGTTC	4703
rs745895961	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151513293	TGACTCAGAAATAAG[A/G]CCAAGATGTCGAGTT	4703
rs745897827	snp	C/G	5.01015e-05	0.00500482	intron-variant	NEB	GRCh38.p7	2:151687388	CAGGGAGTCCATCTT[C/G]AAAACAAGACAGATT	4703
rs745898708	snp	C/T	1.65592e-05	0.00287738	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151643941	CTGGCACTTCTTGGC[C/T]AACACCACCCCCAGC	4703
rs745900657	snp	A/G	4.96948e-05	0.00498447	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151627092	GTCCGGAGGCTGGCG[A/G]TAGATGTTATCACTC	4703
rs745900992	in-del	-/G	9.29239e-05	0.00681566	intron-variant	NEB	GRCh38.p7	2:151617491	AAAAAAAAAAAAAGA[-/G]AGAGAGAGAGAGAAA	4703
rs745903486	snp	C/T	2.90516e-05	0.00381116	intron-variant	NEB, RIF1	GRCh38.p7	2:151516597	GTTAGATATCTCTCC[C/T]CTGGTCAATTCCTAG	4703
rs745909054	snp	C/T	7.70505e-05	0.00620639	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151490396	CTGCAAAGACACCCC[C/T]GTCGCTGTAAGTCGA	4703
rs745912237	snp	A/C	5.10625e-05	0.00505259	intron-variant	NEB	GRCh38.p7	2:151650889	TTTGTATTTATACTG[A/C]AATCAGAGAAAACAC	4703
rs745925059	snp	A/C	1.6563e-05	0.00287771	synonymous-codon	NEB	GRCh38.p7	2:151563657	CACACCAGGGAATTC[A/C]CCGATCACTTTTCCA	4703
rs745931591	snp	A/G	2.35197e-05	0.00342919	intron-variant	NEB	GRCh38.p7	2:151682794	CAAGAGAAAGGTTAC[A/G]TTTCTTTGCTGTGTC	4703
rs745933118	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151560042	TAGAGGATGTATGAT[C/G]TTCTACTATATTTAA	4703
rs745936008	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151676125	AGGCATGACTATATG[A/G]AATATGACATGTAAA	4703
rs745949259	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151542103	ACTTCATGATTGCCA[C/T]GAACACTTCTCTGTA	4703
rs745957152	snp	C/G	1.73622e-05	0.00294632	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151516499	TTGGCAGTGATGTAC[C/G]TTGGTGTTTCAAAGT	4703
rs745959432	snp	A/G	1.65682e-05	0.00287817	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151525216	CCTCTGGTGGCTCCA[A/G]CATGATGGAGTAGTT	4703
rs745972474	snp	C/T	3.32867e-05	0.00407949	missense	NEB	GRCh38.p7	2:151541479	GCCCTCGCTTGGCTC[C/T]TAAAAGATCAGGAGT	4703
rs745986847	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151674220	GGCTGTCAGGGAAAT[G/T]TGTCAGTGAAGGTAA	4703
rs745988264	in-del	-/AAAG	8.28535e-05	0.00643583	intron-variant	NEB, RIF1	GRCh38.p7	2:151505591	GATTTAAAAATGGGA[-/AAAG]AAAGGTATTATTACA	4703
rs745990032	snp	C/G	1.65608e-05	0.00287752	missense, intron-variant	NEB	GRCh38.p7	2:151631187	CCAGCACCTGCTCTA[C/G]AGAATCAGTCACACT	4703
rs745991110	snp	G/T	2.46296e-05	0.00350916	intron-variant	NEB	GRCh38.p7	2:151568041	CAAGGTCCCACTTTT[G/T]CAAAATGCACTCCCA	4703
rs746001580	snp	A/T	4.97822e-05	0.00498885	missense	NEB	GRCh38.p7	2:151690818	TCTGGATGAACTTTG[A/T]AGGTATGCTAGAAAA	4703
rs746008098	snp	A/G	8.28562e-05	0.00643593	missense, intron-variant	NEB	GRCh38.p7	2:151609939	TTCTTGGCCAGCAAG[A/G]TGCTTAACATGTCCA	4703
rs746015217	snp	C/T	1.65641e-05	0.00287781	missense, intron-variant	NEB	GRCh38.p7	2:151627037	TGTTCTTGGCCAGCA[C/T]CTGCTCTAGAGAGTC	4703
rs746029836	snp	G/T	1.65844e-05	0.00287957	intron-variant	NEB	GRCh38.p7	2:151697270	ATGAGGAGAAGAAAT[G/T]AGGCATAAGATGCAG	4703
rs746031384	snp	A/G	7.0629e-05	0.00594218	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151493776	CCTTTCTAAAATACC[A/G]AGCTAAAGTTTTCTT	4703
rs746035711	snp	C/G	1.66095e-05	0.00288175	intron-variant	NEB	GRCh38.p7	2:151692251	GAAAGGTAACCGTGG[C/G]TTTTCGAACCTCACT	4703
rs746040419	snp	A/G	5.73564e-05	0.0053549	intron-variant	NEB	GRCh38.p7	2:151551876	GCATTGTTAGAAGCA[A/G]AGAGAATGGGAACCC	4703
rs746053646	snp	C/T			intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151506290	AGGACAGTGTTAACA[C/T]AGAAGAAAAGAAAAC	4703
rs746053964	snp	A/T	1.65809e-05	0.00287926	missense	NEB	GRCh38.p7	2:151678006	TTCTTAGCCGCCACG[A/T]CATTGAACATATCAT	4703
rs746058844	snp	C/T	1.65798e-05	0.00287917	missense	NEB	GRCh38.p7	2:151662254	TAATAATCTCCATGG[C/T]TTTCTTGTTTTTCTC	4703
rs746062325	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151627329	TTCTTCAATATATGA[A/C]GGCCAAATTGAATAC	4703
rs746067563	snp	A/G	8.3875e-05	0.00647537	intron-variant	NEB, RIF1	GRCh38.p7	2:151526271	ATTTCAGCTTCAGGG[A/G]CAGGAAAAGGGGCAT	4703
rs746068413	snp	G/T	1.65734e-05	0.00287862	missense	NEB	GRCh38.p7	2:151655876	TGGAATCAGTCAGCT[G/T]CTTAAACTGGAAGTT	4703
rs746072690	snp	C/T	1.65726e-05	0.00287855	missense, intron-variant	NEB	GRCh38.p7	2:151618333	GGAGTGTCCGTTATA[C/T]TGGTAAATTTCAGCG	4703
rs746076977	snp	G/T	2.64652e-05	0.00363757	missense	NEB	GRCh38.p7	2:151535708	CATTCATCAATTGAG[G/T]TGCATACTTGAAATG	4703
rs746079973	snp	G/T	2.16668e-05	0.00329134	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151490473	CCACTGATGCTTAGT[G/T]CACTGGCAGATCGTG	4703
rs746083931	snp	A/G	1.92454e-05	0.00310199	synonymous-codon	NEB	GRCh38.p7	2:151560631	CTTGGCGTGTGTCAG[A/G]GACAAGGTGCTGGAA	4703
rs746089985	snp	C/G	1.65597e-05	0.00287743	missense, intron-variant	NEB	GRCh38.p7	2:151640472	TAAGGTCTGGCACTT[C/G]TTGGCCAGCACCACC	4703
rs746090587	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151661703	CCAGAGAACGTCCTG[A/G]TTTGAAATGCTGCTA	4703
rs746096624	snp	A/G			synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151640580	CTTGGCCACGTGCAT[A/G]GACCACATCATCTTG	4703
rs746106936	snp	A/G	0.000148732	0.00862229	intron-variant	NEB	GRCh38.p7	2:151568729	TTTCTATGGGAAAGA[A/G]AGCATCTTTTAGATA	4703
rs746112355	snp	A/G	1.65795e-05	0.00287914	missense	NEB	GRCh38.p7	2:151697194	TCATATTCTTGAGTT[A/G]TGGTCTGAGGGAAGA	4703
rs746117467	snp	C/T	1.65957e-05	0.00288055	missense	NEB	GRCh38.p7	2:151541542	TCTTGCCTGCAGCTC[C/T]GTAGACCAGCTAGAC	4703
rs746122939	snp	C/T	0.000103109	0.0071794	missense, intron-variant	NEB	GRCh38.p7	2:151579340	GCGACACACTTACGT[C/T]GCTCTGTAGGTCGTA	4703
rs746128355	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151566636	GGTTATGTCTTATTC[C/T]CTATCCTAGCTTTAC	4703
rs746132553	snp	A/G	3.31934e-05	0.00407377	intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151534338	CTCAAACATCATAGC[A/G]TATTATAGCAAGAGT	4703
rs746145524	in-del	-/T			intron-variant	NEB	GRCh38.p7	2:151662441	CATTTCATTTGTAAA[-/T]TTTCTGTAACTTTTC	4703
rs746149366	snp	A/C	1.66335e-05	0.00288383	missense	NEB	GRCh38.p7	2:151662178	GCCAAAACCATGTTC[A/C]TCGAGTCCATGAGTG	4703
rs746149494	in-del	-/TG	4.97327e-05	0.00498637	intron-variant	NEB	GRCh38.p7	2:151679866	GTACAACTTAGAGAC[-/TG]TGTTAGTAAAGTCTG	4703
rs746152457	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151613290	ATTTGTCTTCATATG[G/T]ATAATTCATTTTTAA	4703
rs746163908	in-del	-/CTT	3.35323e-05	0.00409451	cds-indel	NEB	GRCh38.p7	2:151695601	AGTTATAGGCATTGA[-/CTT]TGTGCTGGATAAAAG	4703
rs746169321	snp	A/G	5.1351e-05	0.00506684	intron-variant	NEB, RIF1	GRCh38.p7	2:151492316	CTTTATGAAAATATG[A/G]TGGTGTGACTATATC	4703
rs746174952	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151488961	TTATAGTATGTTTTG[C/T]TCTTTTTTAGTTGAG	4703
rs746179104	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151646880	GCCTTGAACTCCCCA[A/C]CTCAGCCTCCCAAAG	4703
rs746179607	snp	A/C	3.32474e-05	0.00407708	missense, intron-variant	NEB	GRCh38.p7	2:151612323	TCTTCACTTTCTCGA[A/C]CTCTACAGAGCCAAT	4703
rs746180925	snp	C/T	5.5588e-05	0.00527171	missense, intron-variant, utr-variant-3-prime	NEB, RIF1	GRCh38.p7	2:151497664	GTTTGACTCTTTCCA[C/T]CTCGGGAGTGACAGG	4703
rs746187473	snp	A/G	0.000311284	0.0124718	missense, intron-variant	NEB	GRCh38.p7	2:151603649	ATTTGAGGGCCTCAG[A/G]CTTTATACGATACAG	4703
rs746193282	snp	C/T	3.35166e-05	0.00409355	intron-variant	NEB, RIF1	GRCh38.p7	2:151524278	TTTATAATCTCCTCA[C/T]ATGAGAGCCACCAGT	4703
rs746203138	snp	G/T	1.7487e-05	0.00295689	missense	NEB	GRCh38.p7	2:151552734	TATCTGTGACAAGCT[G/T]GTAGTCATTCCTTGT	4703
rs746213184	snp	A/G	1.66832e-05	0.00288814	intron-variant	NEB	GRCh38.p7	2:151546489	CATAAGCAAATGTAA[A/G]TCAGGAAACACAAAA	4703
rs746215416	snp	A/G			intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151534671	ACCAACTAAGGCTGT[A/G]AGAATCTCAAAGCAT	4703
rs746218685	snp	C/T	3.31658e-05	0.00407208	missense	NEB	GRCh38.p7	2:151672638	GGCTTCTGAAACCCA[C/T]ATGCTTTCCCTTTGA	4703
rs746220411	snp	A/G	1.65652e-05	0.0028779	missense	NEB	GRCh38.p7	2:151666320	CCACATTCATGTAGT[A/G]AACCAGTTTAGGATC	4703
rs746232620	snp	A/C	0.0108355	0.0728035	missense, intron-variant	NEB	GRCh38.p7	2:151618432	AAGGAATCAATCGGA[A/C]CCCAGCCAATGCCTT	4703
rs746242505	snp	A/G	2.017e-05	0.00317563	missense	NEB	GRCh38.p7	2:151565726	CGTACCTGACTCATC[A/G]TTTCCTGGTTCTTAG	4703
rs746244049	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151621737	ACAAATCATATATAC[C/G]AATGGCTTTTAGCCC	4703
rs746252441	snp	G/T	3.43625e-05	0.00414488	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151526962	CGAGCACCGTGTTTT[G/T]GTCATCAGTGACAGA	4703
rs746257688	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151724723	GCAGCCTCCTTGATG[A/G]ATACAGGTATTGAAC	4703
rs746260041	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151682353	TGTATGCAAGTTATA[C/T]CTTAATAAAATTGTT	4703
rs746260372	snp	A/T			missense, intron-variant	NEB	GRCh38.p7	2:151633824	TGAACTTGGTCTTCC[A/T]CTTCTCAAAGTCCTT	4703
rs746282239	snp	C/T	0.000308547	0.0124168	intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151497072	AAAAACAACCATGAG[C/T]AACATTTCATTTGTT	4703
rs746282255	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151521239	GAAAATGCATTCACA[A/G]TGCTGAGACTCCTTT	4703
rs746286869	snp	A/T	2.10369e-05	0.00324315	missense	NEB	GRCh38.p7	2:151724346	CCTTGGTGTCTTCCC[A/T]GTTCTGCTTGTATAA	4703
rs746289376	snp	C/G	1.65605e-05	0.0028775	missense, intron-variant	NEB	GRCh38.p7	2:151633895	GACCACATCATCTTG[C/G]GGTCATCTTCAATGT	4703
rs746291431	snp	A/G	1.65748e-05	0.00287874	synonymous-codon	NEB	GRCh38.p7	2:151569307	TTTGGCATGATTGAC[A/G]GACACGGAGTCATTT	4703
rs746300613	snp	C/T	2.0976e-05	0.00323845	missense, intron-variant	NEB	GRCh38.p7	2:151620986	CTTCTCAAGTCATAG[C/T]CTTCTTTCTTGGCTT	4703
rs746303798	snp	C/T	1.6623e-05	0.00288292	synonymous-codon, nc-transcript-variant, intron-variant	NEB, RIF1	GRCh38.p7	2:151507002	GTTTTTAAGGTCACA[C/T]TGGTATTGGAGCTAT	4703
rs746304150	snp	A/C/T			intron-variant	NEB	GRCh38.p7	2:151665218	GTCCCCCTCCCACCA[A/C/T]CGGCACGAAGACGAT	4703
rs746327457	snp	C/T	0.001512	0.0274539	intron-variant	NEB	GRCh38.p7	2:151606565	TCTCCCTGCTCGTTT[C/T]GTAGAAAAGAAAAAC	4703
rs746332432	snp	C/T	6.00384e-05	0.00547865	synonymous-codon	NEB	GRCh38.p7	2:151706932	AAGCTGTGGGTTCTC[C/T]GAAGCAGGAAGCACA	4703
rs746334983	snp	A/T	1.65647e-05	0.00287786	missense	NEB	GRCh38.p7	2:151553980	CCATGTCGGGCACGA[A/T]GTGGATTTTCATCTT	4703
rs746337207	snp	C/T	3.97646e-05	0.00445878	missense	NEB	GRCh38.p7	2:151562644	GGCGTTTCGGACGCG[C/T]ATAACATTGGGTTCT	4703
rs746355961	snp	G/T			intron-variant, utr-variant-3-prime	NEB, RIF1	GRCh38.p7	2:151497362	TAGAACTCAGTGGTG[G/T]TATCCACACAAACTG	4703
rs746357379	snp	A/G	1.65611e-05	0.00287755	missense, intron-variant	NEB	GRCh38.p7	2:151643230	ACTTAAATTGATCTG[A/G]GTGCTGACGGTAAAC	4703
rs746361891	in-del	-/CAAAA			intron-variant	NEB	GRCh38.p7	2:151698069	GACTCCGTCTCAAAA[-/CAAAA]CAAAACAAAACAAAA	4703
rs746370157	snp	C/T	3.31647e-05	0.00407201	missense, intron-variant	NEB	GRCh38.p7	2:151650232	CCATGGCATCAGGAA[C/T]GCTGGTGAACTTGTT	4703
rs746376570	snp	A/G	2.46491e-05	0.00351054	synonymous-codon	NEB	GRCh38.p7	2:151565812	CTCCAGGTCAGCTCT[A/G]TAGACATTCTGAGAG	4703
rs746382045	snp	A/G	1.6727e-05	0.00289193	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151485775	CTAAATAGCTTCAAC[A/G]TAGTTGGCTGGGAGC	4703
rs746382270	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151541124	TTCCCCTGATTTTTG[C/T]GTGACTGCATGAAAT	4703
rs746392211	snp	A/C	5.18605e-05	0.00509191	intron-variant	NEB	GRCh38.p7	2:151562568	AGCCAAGACACAGTC[A/C]TGGAAGCTGTAGCTG	4703
rs746394316	snp	A/G	4.97797e-05	0.00498873	missense	NEB	GRCh38.p7	2:151555035	TTTCATATTCTTCCC[A/G]ATATTTGATCTATAG	4703
rs746396853	snp	C/G	1.98206e-05	0.003148	intron-variant	NEB	GRCh38.p7	2:151697697	TCCTGTCACTCCCAC[C/G]CTGATTATAACACTT	4703
rs746405327	snp	C/T	1.65974e-05	0.0028807	intron-variant	NEB	GRCh38.p7	2:151629494	TAATAATCCTGCCTC[C/T]CCACTTCATCCATCC	4703
rs746409121	snp	A/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151527865	TGCCAGTCCAGCCTA[A/T]TCATCTTCAGAATCG	4703
rs746409256	snp	C/T	3.31768e-05	0.00407275	missense	NEB	GRCh38.p7	2:151663760	GGTCTGACTGCATCT[C/T]GGCCACTTGCATGAA	4703
rs746411559	snp	A/G	5.09992e-05	0.00504945	synonymous-codon	NEB	GRCh38.p7	2:151724863	TTGCCTTACCTTACT[A/G]ACTTGCTGCGACACT	4703
rs746415512	in-del	-/GTA	3.31293e-05	0.00406984	cds-indel	NEB	GRCh38.p7	2:151563677	CACTTTTCCAGCCAG[-/GTA]GTAGTGACCTTTCTG	4703
rs746416581	snp	C/T	5.36677e-05	0.00517986	intron-variant	NEB	GRCh38.p7	2:151666438	ACAGAAGTTGGCTAG[C/T]ATAGAAGTCTGATAT	4703
rs746423947	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151563333	GTTTTCCATCCTTTT[A/G]TAACACAGGGTAAAT	4703
rs746430269	in-del	-/A	1.66549e-05	0.00288568	frameshift-variant, intron-variant	NEB, RIF1	GRCh38.p7	2:151492488	GGAAACTATCAGAAT[-/A]AAGAACCTGATGCAG	4703
rs746447333	in-del	-/AC	3.41641e-05	0.0041329	intron-variant	NEB	GRCh38.p7	2:151650901	CTGAAATCAGAGAAA[-/AC]ACAGCTCTTTTAGTA	4703
rs746452808	snp	A/G	1.65726e-05	0.00287855	synonymous-codon	NEB	GRCh38.p7	2:151538188	GACAATGTCTAGGGC[A/G]TCTTTCACCGTGTGG	4703
rs746454129	snp	A/G	8.35541e-05	0.00646297	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151518997	TTGTATTCAGGACAT[A/G]ATTCATGATCAGAGA	4703
rs746456810	snp	A/G/T	5.23934e-05	0.00511805	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151496282	GCCAAGTACCGAGCT[A/G/T]ATATTTTCTTGATTG	4703
rs746461699	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151487469	AAGTGGAACATTACT[A/G]TAAATAATACTGTGA	4703
rs746464274	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151591209	CAGATTGTAAGAGTT[A/G]TTCTTGAATTTAGGA	4703
rs746479662	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151527718	AAGAGGAAGCCCCAA[C/T]TGAAATTTCTGTACA	4703
rs746481799	snp	C/T	9.22552e-05	0.0067911	intron-variant	NEB	GRCh38.p7	2:151655265	TAATTTTTATATAAA[C/T]TTACCTGACTATACA	4703
rs746490267	snp	A/G	1.68937e-05	0.0029063	intron-variant	NEB	GRCh38.p7	2:151549751	AGATTCTGCAGGAAT[A/G]AGGAAGAGCAGGTTA	4703
rs746498723	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151664955	CAACTCCATGGTAAA[A/T]GAGGTTAAATGGATA	4703
rs746502484	snp	A/G	1.92369e-05	0.0031013	missense	NEB	GRCh38.p7	2:151684926	TGGAGCATATCAAGA[A/G]GTGCCGTGTAGATAG	4703
rs746505680	snp	C/T	1.65496e-05	0.00287655	intron-variant	NEB	GRCh38.p7	2:151672360	GGGTCTGTTGTTACA[C/T]ATACTTACATCACTC	4703
rs746507330	snp	C/T	3.31241e-05	0.00406952	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151526056	GCTTCTTGACATGGT[C/T]CTTGTACTTGTTCTG	4703
rs746519954	snp	A/G/T	6.62098e-05	0.00575331	missense, intron-variant	NEB	GRCh38.p7	2:151617413	ATGATTTCTGGTGTA[A/G/T]CAGGCATGACATGAA	4703
rs746524043	snp	C/T	1.68601e-05	0.00290341	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151534167	ACATCTCATGAGAAA[C/T]TGGGAGCACAGTCCT	4703
rs746528654	snp	A/G	1.69358e-05	0.00290992	intron-variant	NEB	GRCh38.p7	2:151568462	GCAAGTTACTTGTTA[A/G]GAAAGCATCATGTTG	4703
rs746533704	in-del	-/GT			intron-variant	NEB	GRCh38.p7	2:151630205	ATATTAATAAACCAC[-/GT]GTCTATAAAATTGCA	4703
rs746541315	in-del	-/TTTTTTTTTTTTTTT			intron-variant	NEB, RIF1	GRCh38.p7	2:151524655	ACTCAAGAGAGAGGC[-/TTTTTTTTTTTTTTT]TTTTTTTTTTTTTTT	4703
rs746541595	in-del	-/AAGCC	1.65888e-05	0.00287996	frameshift-variant	NEB	GRCh38.p7	2:151663810	TCTTCCAGGCTCCGG[-/AAGCC]AATGTGTTTCCCTTT	4703
rs746552340	snp	A/G	1.65652e-05	0.0028779	missense	NEB	GRCh38.p7	2:151568360	CAGTGTGCAGCAGGG[A/G]GGTTTCTGTGAGGGT	4703
rs746558524	snp	A/G	1.6563e-05	0.00287771	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151505551	GGAGTTCCTTGTCCT[A/G]TTGCTTCCTTATACT	4703
rs746559281	in-del	-/T			intron-variant	NEB	GRCh38.p7	2:151662115	ATGCATATGAAACAC[-/T]GCATTATTGAAAGAC	4703
rs746567958	snp	C/T	3.34885e-05	0.00409184	splice-acceptor-variant, intron-variant	NEB	GRCh38.p7	2:151631347	TGACTTGTAAATATT[C/T]TGAGCAGAGGAAAAA	4703
rs746575438	snp	A/G	3.32165e-05	0.00407519	missense	NEB	GRCh38.p7	2:151576203	ACTTCAGGTGTGTCA[A/G]CAATGCTTGTGTACT	4703
rs746579007	snp	C/T	3.50085e-05	0.00418366	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151494248	CACATTTTCTTTGTA[C/T]AAAACCTATGGGAAT	4703
rs746581105	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151716943	ATAGGTAGACTAAGC[C/T]GTTTGTTAGGGCCTT	4703
rs746587041	snp	A/C	1.65839e-05	0.00287953	intron-variant	NEB	GRCh38.p7	2:151697469	TTTTCTGCAAGACAA[A/C]ACATACTTCATTTAT	4703
rs746594174	snp	C/T	1.65798e-05	0.00287917	intron-variant	NEB	GRCh38.p7	2:151692044	TGAGGCATGAACCAT[C/T]GTCTTCAAACTTACA	4703
rs746598121	snp	A/G			intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151506826	ATGTTAATTGTGTGT[A/G]TCAATATAAGGCTAG	4703
rs746602928	snp	A/C	1.65597e-05	0.00287743	missense, intron-variant	NEB	GRCh38.p7	2:151627666	CCACTCCCAGCATGT[A/C]CACTGGGCTGCTGAA	4703
rs746606383	in-del	-/AGT			intron-variant	NEB, RIF1	GRCh38.p7	2:151495630	CGGGAAATGGTTTAC[-/AGT]TAAAGTTTGCAGTTA	4703
rs746609595	snp	A/G	4.21434e-05	0.0045902	intron-variant	NEB	GRCh38.p7	2:151610876	TAAATGCTACAGGGC[A/G]GGGCGGCATGGGGCA	4703
rs746614628	snp	A/G	2.29371e-05	0.00338645	intron-variant	NEB	GRCh38.p7	2:151537857	TATGTGAAAATAGAA[A/G]ATGTCAACACTCACA	4703
rs746617401	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151492990	GAGTATTACCCATGT[C/T]ATAAAGTATCTTAAA	4703
rs746622217	snp	C/T	2.51468e-05	0.00354581	missense	NEB	GRCh38.p7	2:151561222	CCTCACTGGCATTAA[C/T]GCCACTCTGAACAGC	4703
rs746623312	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151619015	CTGGTTTCGAAAAAC[A/G]TAAGAATGATAGAAT	4703
rs746625254	snp	A/C	1.80527e-05	0.00300433	intron-variant	NEB	GRCh38.p7	2:151679697	ATTTTCTAGTTGCCC[A/C]TGTATGACCACAGCT	4703
rs746625486	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151667237	TTAAAATACTTGGAG[A/T]CTTTTCTAATTTAGT	4703
rs746629795	snp	C/G/T	0.000137611	0.00829397	intron-variant	NEB	GRCh38.p7	2:151646110	CTTTCTGAAAACACA[C/G/T]GCTGAATTTGAAAAC	4703
rs746641050	snp	C/T	8.81174e-05	0.00663709	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151591363	ATCACTGGCAATATC[C/T]CTGGAAGCCTTGGCA	4703
rs746641192	snp	A/G	3.71733e-05	0.00431107	intron-variant	NEB, RIF1	GRCh38.p7	2:151519089	GTGTTATGGGGGAAG[A/G]AAGGAAATCACGTAA	4703
rs746644593	snp	A/C	3.33017e-05	0.00408041	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151642628	AGGAATGGCATCTAC[A/C]CGCATGTCATAACCT	4703
rs746651854	snp	C/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151500233	GTGGGACCAAAGAAA[C/G]TTACTGATCTAATTA	4703
rs746674977	snp	G/T	4.11024e-05	0.00453315	intron-variant	NEB	GRCh38.p7	2:151723361	TGCACACCTAAGTGG[G/T]GCCACTTGCATTTCA	4703
rs746675517	snp	C/T	7.7824e-05	0.00623746	intron-variant	NEB	GRCh38.p7	2:151565175	AAACCAAATCTTTTA[C/T]TACTATAAATGAATA	4703
rs746686431	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151731769	GGGATATTTAAGTTG[C/G]AGAGTAAAAACTGTT	4703
rs746691476	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151539507	TCCTAGAGCTATGTT[A/G]CTAAGTTGAGGGGGT	4703
rs746700725	in-del	-/CT	0.000145066	0.0085154	intron-variant	NEB, RIF1	GRCh38.p7	2:151531754	GTTTGCAGATGCCCC[-/CT]GAGTTTGAGAAGGTA	4703
rs746705215	in-del	-/A			intron-variant	NEB	GRCh38.p7	2:151637698	TGACTAGCTAGACAC[-/A]GGGGGAGCCCTTTGT	4703
rs746719652	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151653614	ATAAAATCTATCAGC[A/G]TCAGTTTGTTGAGGT	4703
rs746733372	snp	C/T	6.88006e-05	0.00586477	intron-variant	NEB	GRCh38.p7	2:151546308	GGGCATCCAGCTGTG[C/T]GGGGGGTAATTATGC	4703
rs746737604	snp	C/T	5.2946e-05	0.00514492	missense	NEB	GRCh38.p7	2:151570350	CTGTGAGGGTGCCCA[C/T]GTAGTGTCCCTTCTG	4703
rs746738114	snp	C/T	1.65616e-05	0.00287759	missense, intron-variant	NEB	GRCh38.p7	2:151614419	CCACCCCCAGCATGT[C/T]CACTGGGCTGCTGAA	4703
rs746755643	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151668967	CTCAGAGCAAGAGTT[A/G]CAAAGAACCAGAAAG	4703
rs746761307	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151550507	TGTTGACATCAGGCC[A/G]TGAAGAGGTCAGGAT	4703
rs746761562	snp	C/T	1.65993e-05	0.00288086	missense	NEB	GRCh38.p7	2:151663655	CATTGGTGGCCACTT[C/T]CTGAGACTTCTTGGC	4703
rs746768491	snp	C/T	3.51877e-05	0.00419436	intron-variant	NEB, RIF1	GRCh38.p7	2:151502783	TTTTTTTTGGCCCCC[C/T]AAGAAATACCGAGCT	4703
rs746777409	snp	A/G	5.13518e-05	0.00506688	intron-variant	NEB	GRCh38.p7	2:151561362	ACATACAGGTCTGTC[A/G]TCAGCTGTAGCTGCT	4703
rs746779495	in-del	-/TAT			intron-variant	NEB, RIF1	GRCh38.p7	2:151485961	ATGGAAAAGGGGAAA[-/TAT]TATATGTTGGATTTG	4703
rs746795048	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151574988	CAAGCAATCCTCTGG[C/T]CTTGACCTCCCAAAG	4703
rs746809883	snp	C/T			missense	NEB	GRCh38.p7	2:151663607	TGGCATCAGGAAGCA[C/T]GTTGTAGGTATGGAT	4703
rs746813930	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151677360	AGTTAAAAAGGAAAA[G/T]TTTTTAAAAAGGAAG	4703
rs746816609	snp	A/G	4.96915e-05	0.0049843	synonymous-codon	NEB	GRCh38.p7	2:151674549	CACATTGTTGCCCTT[A/G]GCTATTAAGTCATAC	4703
rs746822265	snp	C/T	3.3123e-05	0.00406945	missense	NEB	GRCh38.p7	2:151666188	TGTAGTTGGCGTTGG[C/T]GGCAACCTCCTGAGA	4703
rs746834957	snp	A/G	5.3118e-05	0.00515327	intron-variant	NEB, RIF1	GRCh38.p7	2:151527601	CTGTTTTTAACAGGA[A/G]AGAAAGGAATCACTT	4703
rs746838787	snp	C/T	1.92007e-05	0.00309838	intron-variant	NEB	GRCh38.p7	2:151642735	GCATTGTAAGGAAAA[C/T]GTATCACGCACTATG	4703
rs746838940	snp	C/T	1.6563e-05	0.00287771	missense	NEB	GRCh38.p7	2:151694429	TCATAGTCTTTCTTG[C/T]ACATCACCTGCAAAG	4703
rs746855707	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151709185	TCAGTGGGAAAATAA[A/G]AAAAATAATGATAGT	4703
rs746862475	snp	C/T	1.71185e-05	0.00292557	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151512757	AAGATTCTTGACTTG[C/T]TGGGCATGAATGATC	4703
rs746866602	snp	A/G	1.65608e-05	0.00287752	missense, intron-variant	NEB	GRCh38.p7	2:151627753	CCACATGCATGGACC[A/G]CATCATCTTGGGGTC	4703
rs746875695	snp	C/T	1.66239e-05	0.00288299	intron-variant	NEB	GRCh38.p7	2:151690720	TTGCATAAATCAAAG[C/T]ACTTACATCACTAAG	4703
rs746880032	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151527379	TCGGATCTCAAACGA[A/G]CAAGGGTTAACACTC	4703
rs746885793	in-del	-/TTG			intron-variant	NEB, RIF1	GRCh38.p7	2:151510636	TTTTATTACAGTATA[-/TTG]TTATAATTGTTCTAT	4703
rs746894401	snp	A/C	1.6671e-05	0.00288708	intron-variant	NEB	GRCh38.p7	2:151630847	ATAAGATGCTGATTA[A/C]AAATCATTTGAAATA	4703
rs746895397	snp	C/T	1.93883e-05	0.00311348	intron-variant	NEB	GRCh38.p7	2:151727648	TGAGATAAGTAATTT[C/T]TTAATAATCAAGCCA	4703
rs746898531	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151560114	TTTATATCTAAGAAA[A/T]GTTCTACCTAAAAAA	4703
rs746898612	snp	A/G	5.53557e-05	0.00526068	intron-variant	NEB	GRCh38.p7	2:151547784	TTAGTAGGGGACGAC[A/G]AGGGCATCTACTGAC	4703
rs746902887	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151726088	TTCTTGCTTTAATGA[A/T]AATGTGCATAATTTA	4703
rs746910220	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151640867	ATAAAATATATACCA[C/T]ATAGATAGGCATTAC	4703
rs746912117	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151688563	CATCCCCTATTTCAG[A/G]GACTGTGGCACAGTC	4703
rs746929676	snp	C/G	1.65611e-05	0.00287755	missense, intron-variant	NEB	GRCh38.p7	2:151650745	GAACTTAGTTTTCCA[C/G]TTCTCAAAGTCCTTC	4703
rs746929871	snp	A/T	1.77944e-05	0.00298276	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151502872	CCTTTCCCCAAATTT[A/T]CTTTGTACAAAACCT	4703
rs746940000	snp	A/G	3.32215e-05	0.00407549	intron-variant	NEB	GRCh38.p7	2:151710427	CAGCCATCCCTTCCC[A/G]CTTAACTGTGCTAAT	4703
rs746940820	snp	G/T	1.82871e-05	0.00302377	intron-variant	NEB, RIF1	GRCh38.p7	2:151524664	AGAGGCTTTTTTTTT[G/T]TTTTTTTTTTTTTTT	4703
rs746963507	snp	A/T	1.8013e-05	0.00300103	missense	NEB	GRCh38.p7	2:151694523	CAGGCCACACTCACA[A/T]CGCTGGTGTTCTTGG	4703
rs746969189	snp	C/T	1.6571e-05	0.0028784	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151529257	CTTTGATATGAACAG[C/T]ATCTGGCTCAATGGT	4703
rs746969300	snp	C/G	7.13598e-05	0.00597284	intron-variant	NEB	GRCh38.p7	2:151675248	CTATAATTTTATTGT[C/G]AGGTCCGAATTTCAC	4703
rs746981514	in-del	-/A/AA	0.00161777	0.028403	splice-acceptor-variant, intron-variant	NEB	GRCh38.p7	2:151617470	CAGTATATAAGCGCT[-/A/AA]ACAAAAAAAAAAAAA	4703
rs746993173	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151547139	GAGGCCACACAGGGA[G/T]TTAGGGAGTGAGGAG	4703
rs746996111	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151553197	TCTCCACCAGAGGAC[A/G]ATGGCACACCTGGAC	4703
rs746999970	snp	C/T	5.16596e-05	0.00508204	splice-donor-variant	NEB	GRCh38.p7	2:151675286	CAAAGACCCTACTTA[C/T]GTCACTTATATTGTA	4703
rs747014548	in-del	-/A			intron-variant	NEB, RIF1	GRCh38.p7	2:151514709	TGAGAACCCAATTTG[-/A]AAACCCACAGTTAGG	4703
rs747014723	snp	C/T	1.65737e-05	0.00287864	synonymous-codon	NEB	GRCh38.p7	2:151569322	GGACACGGAGTCATT[C/T]GGCATCCACCCAATT	4703
rs747017871	snp	A/G	1.68012e-05	0.00289833	intron-variant	NEB	GRCh38.p7	2:151669134	CCTTGTAGTTCAACT[A/G]AAAACAAAGGAGACA	4703
rs747026163	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151712911	AAAGGTTAGGGGGAA[A/T]CCTTTCTCTCCAAAC	4703
rs747030280	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151548139	ATTACCAAATACAAA[A/G]AACCACTACCAAGAA	4703
rs747034126	snp	A/T	1.72662e-05	0.00293817	missense	NEB	GRCh38.p7	2:151553841	ACATCGCTGATCTGA[A/T]CTGTGACTTTCCTGA	4703
rs747035666	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151661950	TGGTTCATTGAAGAT[C/T]TGAAGACTACTAGTT	4703
rs747044882	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151670752	TAATGTTATTTCATA[C/T]GTATAATGCGTATCT	4703
rs747045452	snp	A/G	3.36689e-05	0.00410284	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151507038	AAGAGTAAACATCTT[A/G]TTAAGATTTCAACAT	4703
rs747051653	snp	G/T	1.6666e-05	0.00288664	intron-variant	NEB	GRCh38.p7	2:151644422	GAGACTGCTTTGAAG[G/T]GATAAATTGCAATCA	4703
rs747055614	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151533729	GACTGCAATGCTTGC[A/G]GTTGGCCATTCATAG	4703
rs747055828	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151572278	AGCAAGCTGAGATCA[C/T]GCCACTGTACTCCAG	4703
rs747063282	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151613355	TAAGTTAAATAGACA[C/T]AAAATTATAATGCAA	4703
rs747066360	in-del	-/AG			intron-variant	NEB, RIF1	GRCh38.p7	2:151503571	TAACATTCAAGGAAC[-/AG]GGGGGAAAATTCCAT	4703
rs747068363	snp	A/G	2.56269e-05	0.0035795	intron-variant	NEB	GRCh38.p7	2:151560959	TACTGTCCCAGAAGG[A/G]GGAAAGGTGGCTCAT	4703
rs747069226	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151631706	TTAGTGAATCAATTT[C/T]AGGCCGAGGCAAATG	4703
rs747090172	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151628615	GGAAGCCGAGGGAGG[C/T]GGATCGCCTGAGGTC	4703
rs747091795	snp	C/T	3.36973e-05	0.00410457	missense	NEB	GRCh38.p7	2:151665421	TTCTCGGGGTGCTGG[C/T]GATACTTCTTCTCAC	4703
rs747094514	snp	A/G	1.83481e-05	0.00302882	missense	NEB	GRCh38.p7	2:151684810	ATGCCTTCTTGGCAA[A/G]GTCCACATTGATGCT	4703
rs747100290	snp	C/T	1.67567e-05	0.00289449	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151506904	AAAATAAATAGTAAA[C/T]ATACCGAGCTGAAAT	4703
rs747100627	snp	C/T	1.65616e-05	0.00287759	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151518377	GATTATCGGGTATGG[C/T]GTGGTAGTGGCCTTT	4703
rs747101480	in-del	-/C	0.000162193	0.00900389	intron-variant	NEB, RIF1	GRCh38.p7	2:151514803	GAGGGAAAGAAAAGA[-/C]CAAGTGGGCACTACC	4703
rs747102490	snp	C/T	1.65822e-05	0.00287938	missense	NEB	GRCh38.p7	2:151678019	CGACATTGAACATAT[C/T]ATGGGGCGTGTTGTA	4703
rs747108920	snp	A/T	5.37062e-05	0.00518172	intron-variant	NEB	GRCh38.p7	2:151568218	GGTTAAAATGAGGAG[A/T]CAGAAGGGAGGGGTA	4703
rs747118508	snp	A/G	1.67441e-05	0.0028934	intron-variant	NEB	GRCh38.p7	2:151627229	ATTAAACACAAAAGC[A/G]AGTATTACTGAAGTT	4703
rs747127559	snp	C/T	1.65806e-05	0.00287924	intron-variant	NEB	GRCh38.p7	2:151697290	ATAAGATGCAGCCAT[C/T]GTATTCATGCCCTGA	4703
rs747131655	snp	G/T	3.31225e-05	0.00406941	missense, intron-variant	NEB	GRCh38.p7	2:151640606	TCTTGGGGTCATCAC[G/T]TATAGCTCGGGCACC	4703
rs747133507	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151503874	ATTTTCTTTTTGTTT[C/T]GTATGTTCTAATGAA	4703
rs747134879	snp	C/G	2.65009e-05	0.00364002	synonymous-codon	NEB	GRCh38.p7	2:151547498	CAGAGAGATCATGTG[C/G]CCCTGCATCTTGAAG	4703
rs747146562	snp	G/T	2.43442e-05	0.00348877	missense	NEB	GRCh38.p7	2:151535728	TACTTGAAATGCCTA[G/T]TGATCGGAGAGTCGG	4703
rs747159745	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151644864	TAGGTGATTTTGTCC[G/T]TGTGGGAACATCACA	4703
rs747168854	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151713875	GGAAGGCTGGCAAAC[A/G]GAAGGTAACATTAGT	4703
rs747179265	snp	A/G	2.17238e-05	0.00329567	stop-gained, intron-variant	NEB, RIF1	GRCh38.p7	2:151490486	GTGCACTGGCAGATC[A/G]TGACTGCTCCCGGCT	4703
rs747180990	snp	C/T			upstream-variant-2KB	NEB	GRCh38.p7	2:151736061	GATATTGACATAAAT[C/T]GATATACTTAATATG	4703
rs747186813	snp	A/G	4.6619e-05	0.00482776	synonymous-codon	NEB	GRCh38.p7	2:151687661	TGGCTTTGGCTGCCA[A/G]CAGGGGAATGGCGTC	4703
rs747188236	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151673025	GGGTTTCATAGGTTT[C/T]GATTTAATATGTTAT	4703
rs747193550	snp	A/T	1.68838e-05	0.00290544	intron-variant	NEB	GRCh38.p7	2:151553361	TAGACTATGGAGAAA[A/T]GGAAATATACTAAAG	4703
rs747203833	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151614800	CAGGTGGCAGCATGA[A/G]CCTAGAATGAAGAGC	4703
rs747207078	snp	A/G	1.66405e-05	0.00288443	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151612339	CTCTACAGAGCCAAT[A/G]GGAACCCATCCTATG	4703
rs747213004	snp	G/T	3.31576e-05	0.00407157	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151650254	GAACTTGTTTCTGTC[G/T]GGAGGCTGACGATAT	4703
rs747215131	snp	C/T	7.14107e-05	0.00597497	synonymous-codon	NEB	GRCh38.p7	2:151656159	AAGCCTTACATCACT[C/T]TGTATGCGATTCATA	4703
rs747222372	snp	C/G	3.92881e-05	0.00443199	missense	NEB	GRCh38.p7	2:151565751	TCTTAGTAACCCTTA[C/G]ATGGTCCACAGAATC	4703
rs747223492	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151490359	TGCCAAAATCAGCGC[C/T]AGGCACTTGTACCTG	4703
rs747225286	snp	A/G	6.71704e-05	0.00579489	missense	NEB	GRCh38.p7	2:151724873	TTACTGACTTGCTGC[A/G]ACACTTTCTTTGCAT	4703
rs747225838	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151620771	TGTGATGCTTGTGAT[C/T]TTGGGCAAGTTATCT	4703
rs747227019	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151618205	ATCTTTAAAATGCAA[A/T]AATATATCAGAATTT	4703
rs747227602	snp	A/G	1.65996e-05	0.00288089	intron-variant	NEB, RIF1	GRCh38.p7	2:151524300	GCCACCAGTGCACCC[A/G]TCTGCATTACCTGGC	4703
rs747230092	in-del	-/CAAA	3.31362e-05	0.00407026	intron-variant	NEB	GRCh38.p7	2:151697327	TGTTATTTGGAAAGT[-/CAAA]CAATTGTCTTAGAAC	4703
rs747230349	snp	C/G	3.56837e-05	0.00422381	intron-variant	NEB	GRCh38.p7	2:151619446	CTAACATCAAGGAAA[C/G]TTACGTCACTCTGGA	4703
rs747237399	snp	A/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151521394	GCTCTTCTCTGAAAA[A/T]GTTTCACTCTCAACA	4703
rs747246143	snp	C/T	1.66715e-05	0.00288712	missense, intron-variant	NEB	GRCh38.p7	2:151640663	AGCCTTCTTTGTACT[C/T]GAACTAAAAGAAGAA	4703
rs747252722	snp	A/G	0.000188326	0.00970192	intron-variant	NEB	GRCh38.p7	2:151633985	AATGAAAATGCACAA[A/G]TCAGGTTTTTATTGT	4703
rs747254061	snp	A/T	1.77461e-05	0.00297871	missense	NEB	GRCh38.p7	2:151692355	TCATAGTTTTCCTTG[A/T]ATAATCTCTGTTAAA	4703
rs747256555	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151696110	TATTGAGGTCACTTT[C/T]ATTTTTTTAGTTCAA	4703
rs747263642	in-del	-/A	1.66334e-05	0.00288382	intron-variant	NEB	GRCh38.p7	2:151725441	CTCCTTTATTTCAGC[-/A]ATGCAGCCCACCTCA	4703
rs747277167	snp	A/G	0.00013249	0.00813802	synonymous-codon	NEB	GRCh38.p7	2:151697353	CTTAGAACTTACATC[A/G]CTGTTTTGAGCTGTG	4703
rs747277690	snp	A/G	1.69766e-05	0.00291342	synonymous-codon	NEB	GRCh38.p7	2:151667894	AATGGTTTTCTTCCA[A/G]TCTGCTTTATAATGA	4703
rs747277701	in-del	-/ATG			intron-variant	NEB, RIF1	GRCh38.p7	2:151511778	GGAGAGTTATTCATC[-/ATG]AGGGGAGTCAGGGGT	4703
rs747282057	in-del	-/TGTAGCCATAGGCC	1.94369e-05	0.00311738	frameshift-variant	NEB	GRCh38.p7	2:151563885	AGCGCTCATCCAGGG[-/TGTAGCCATAGGCC]TTGGTGCCCTCCCAC	4703
rs747282707	snp	C/T	0.000146322	0.00855216	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151527000	CAACCCTTGAGGAAC[C/T]CCCGGTCCAGCTTAT	4703
rs747303590	snp	A/G	4.97583e-05	0.00498765	missense	NEB	GRCh38.p7	2:151672641	TTCTGAAACCCACAT[A/G]CTTTCCCTTTGACTT	4703
rs747306079	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151569757	AAAAGCATGTCTGTG[A/C]CTACATCCTGTCCAT	4703
rs747307404	snp	A/G	1.70822e-05	0.00292247	intron-variant	NEB	GRCh38.p7	2:151663890	AAATTATGGTGATGA[A/G]AATGGTAAAAGAGAA	4703
rs747323786	snp	C/T	1.65685e-05	0.00287819	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151485885	CATCCTTGAAGGACA[C/T]CTCATCTGCATCAGC	4703
rs747324129	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151635105	TGCTTAAACAATCCT[C/G]AAAATGGGGATAATG	4703
rs747326135	snp	C/T	3.33006e-05	0.00408034	missense	NEB	GRCh38.p7	2:151662334	GCATAGTCAGCCTTG[C/T]ACTGATTCTGCAAAA	4703
rs747329222	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151683235	ACTAAGTATTTGCAC[A/G]CATGGCCCTTCATGT	4703
rs747337656	snp	C/G	9.95652e-05	0.00705498	missense, intron-variant	NEB	GRCh38.p7	2:151650361	CTCTCAGCCACTCAA[C/G]GTCAGATTTATATAG	4703
rs747342665	snp	G/T	1.66596e-05	0.00288609	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151492491	AACTATCAGAATAAA[G/T]AACCTGATGCAGGAG	4703
rs747346453	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151719634	TCACGCCTGTAATCC[A/C]AGCACTTTGGGAGGC	4703
rs747349612	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151618269	CAGTGAGGATTGAAG[A/G]CTCACCTTATTCATG	4703
rs747362775	snp	G/T	0.000144155	0.00848861	intron-variant	NEB	GRCh38.p7	2:151684733	AAAGTCCATTTCAGT[G/T]TCCATCTTTTTAAAA	4703
rs747370639	snp	A/C/T			intron-variant	NEB	GRCh38.p7	2:151555154	CTGAGATCCACCCAG[A/C/T]GTTGGGGACAACACT	4703
rs747383643	snp	C/T	1.99647e-05	0.00315942	synonymous-codon	NEB	GRCh38.p7	2:151562659	TATAACATTGGGTTC[C/T]TCCAGAAGAGACGTC	4703
rs747388026	snp	A/T	1.94139e-05	0.00311554	intron-variant	NEB	GRCh38.p7	2:151688253	CATTTTCTCTTTTCA[A/T]GTACACCAAACATAG	4703
rs747394409	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151720870	TCACTTTGTTCTGAT[A/G]ACTCTCAAATATTAA	4703
rs747398931	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151647680	ACCAGAAAACCCAAA[C/T]GGAGGGAGATTCTAC	4703
rs747404777	snp	A/C	1.68221e-05	0.00290014	intron-variant	NEB	GRCh38.p7	2:151538292	AAACTACCAAGTTAA[A/C]TAATTGAGCTCTTTT	4703
rs747405149	in-del	-/TG	2.33252e-05	0.00341498	frameshift-variant, intron-variant	NEB, RIF1	GRCh38.p7	2:151496296	TAATATTTTCTTGAT[-/TG]TGTTTGACTCGCTCC	4703
rs747414141	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151622125	CGTGCCTCAGCCACC[C/T]GAGTAGCTGGGATTA	4703
rs747415022	snp	C/T	3.3054e-05	0.00406521	intron-variant	NEB	GRCh38.p7	2:151565840	GAGCAGGAAGAGAGA[C/T]ATAATGGAGGAATAA	4703
rs747423578	snp	C/T	5.02121e-05	0.00501034	missense	NEB	GRCh38.p7	2:151724951	ACATCACCATCCATT[C/T]GATACTTAACCTGCC	4703
rs747423590	snp	C/T	3.45871e-05	0.00415841	missense	NEB	GRCh38.p7	2:151706955	GAAGCACATTATAAT[C/T]TGCTTTTCCTTTATT	4703
rs747425038	snp	C/G/T	6.62815e-05	0.00575647	missense	NEB	GRCh38.p7	2:151554962	CCAACTCGGAGGCAC[C/G/T]GTGCTGTGTTCGGAT	4703
rs747430602	snp	C/T	5.76076e-05	0.00536661	intron-variant	NEB	GRCh38.p7	2:151667764	TTGAACTCCTGAAGT[C/T]TTTTAGATAGAAAGT	4703
rs747434554	in-del	-/AGA	1.92406e-05	0.0031016	intron-variant	NEB	GRCh38.p7	2:151570414	ATGCAAAAATAAAGC[-/AGA]TGGGTCACAGCATGT	4703
rs747440264	snp	A/T	3.37223e-05	0.00410609	intron-variant	NEB	GRCh38.p7	2:151614261	CCATTACTGAAGAAT[A/T]TTAGAGCCACTCACA	4703
rs747450126	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151729154	CTGAGTAGCATTTCA[A/G]TGCATCATCAGGGAC	4703
rs747458739	snp	A/G	8.28233e-05	0.00643465	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151629602	GTCACTTCGCAAGTC[A/G]TAGCCTTTCTTTTTT	4703
rs747459591	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151657180	CAGCGTAATAGAGGG[A/G]AGAAGAATTTGGAGT	4703
rs747461174	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151542192	ACCATTCTTCCCTAG[G/T]TGGCTTCCTGTCTTT	4703
rs747461182	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151556682	CTAAATATATACACA[A/C]CCAACACAGGAGCAC	4703
rs747464189	snp	A/G	1.79255e-05	0.00299373	missense, intron-variant	NEB	GRCh38.p7	2:151625620	TCTTGTCTTTGTCCC[A/G]GGCTTCTGTGTATAA	4703
rs747465260	snp	A/G	0.000120431	0.00775893	intron-variant	NEB	GRCh38.p7	2:151549621	ACCCATCTCAATGAG[A/G]AGGAGACCACTCACA	4703
rs747466015	snp	A/G	8.28397e-05	0.00643529	missense, intron-variant	NEB	GRCh38.p7	2:151640056	AGATCAGACTTGTAC[A/G]TATTCTGTTGACACA	4703
rs747472693	snp	A/G	1.65614e-05	0.00287757	synonymous-codon	NEB	GRCh38.p7	2:151677640	GGTAAATTTGAGGGT[A/G]TCTGGATGTTGCCTG	4703
rs747474929	snp	A/G	0.000942951	0.021693	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151498393	CAAAAAAAGCAATCA[A/G]TCAGTCATTTTCCCC	4703
rs747479662	snp	C/T	1.94604e-05	0.00311926	intron-variant	NEB	GRCh38.p7	2:151727923	TGAAAATTTGATATG[C/T]AGTTCAACATTGTTG	4703
rs747482412	snp	G/T	1.83643e-05	0.00303015	intron-variant	NEB	GRCh38.p7	2:151643362	ACAAATTCTGAAAGT[G/T]CAAGTGACAAATTTG	4703
rs747483703	snp	C/T	1.65745e-05	0.00287871	missense	NEB	GRCh38.p7	2:151659075	CTTACATCACTCATA[C/T]TAATTGCATTTGCCT	4703
rs747498755	snp	A/C/G	8.29502e-05	0.00643965	intron-variant	NEB	GRCh38.p7	2:151575830	AAAATAATAAAATTA[A/C/G]TTCACAATTTTCATG	4703
rs747500560	snp	A/G	1.6795e-05	0.0028978	synonymous-codon	NEB	GRCh38.p7	2:151695635	AGGAGTATCAGGGGG[A/G]ATATGGCACTTGAAC	4703
rs747503023	snp	A/G	1.65633e-05	0.00287774	synonymous-codon	NEB	GRCh38.p7	2:151671095	ACTTGTGAACTTGAC[A/G]GTATCTGGGTGCTGT	4703
rs747504576	snp	A/G	9.94283e-05	0.00705012	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151529268	ACAGCATCTGGCTCA[A/G]TGGTGCAGTTGGATT	4703
rs747505579	snp	G/T	1.65625e-05	0.00287766	synonymous-codon	NEB	GRCh38.p7	2:151680802	CGAGGTAAACTTGAG[G/T]GTGTCTGGATGTTGG	4703
rs747506458	snp	A/C	4.76497e-05	0.00488084	intron-variant	NEB	GRCh38.p7	2:151630687	GACACCACCACCACA[A/C]TATAGCACCACAGAT	4703
rs747518320	snp	A/G	1.68769e-05	0.00290485	intron-variant	NEB, RIF1	GRCh38.p7	2:151485969	GGGGAAATATTATAT[A/G]TTGGATTTGCAACAG	4703
rs747521866	snp	G/T	1.66327e-05	0.00288376	intron-variant	NEB, RIF1	GRCh38.p7	2:151505437	GTAGCAATTGAGAGA[G/T]GGCCAGTCACACAAA	4703
rs747522554	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151708495	CCTCTCCTGATTTTG[C/T]TTCTCCCTCATCTTA	4703
rs747529091	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151558574	GCTAAAGTAATAAAA[A/T]CACCATGGTACTTTT	4703
rs747545945	snp	A/T	6.25489e-05	0.005592	intron-variant	NEB	GRCh38.p7	2:151709634	TCAAACCATCAAGAT[A/T]AATGGGATGATTTCC	4703
rs747546709	snp	A/G	3.31576e-05	0.00407157	missense, intron-variant	NEB	GRCh38.p7	2:151643844	GGTCATAGGCCTGCC[A/G]AGCATGGATGACATC	4703
rs747553930	in-del	-/A	1.67556e-05	0.0028944	intron-variant	NEB	GRCh38.p7	2:151677842	GGCTCTGAACTTAAT[-/A]AGGGGGGTTTCTTGA	4703
rs747554265	snp	C/G	1.66172e-05	0.00288242	intron-variant	NEB	GRCh38.p7	2:151625501	GCAACAATCAATGTG[C/G]CCAGACCAAAGAAAT	4703
rs747562571	snp	A/G	3.81417e-05	0.00436685	intron-variant	NEB	GRCh38.p7	2:151540496	TTAAGTGTCTTCCCA[A/G]TTTCCAACCAAGCCA	4703
rs747564597	in-del	-/TCTT	5.83005e-05	0.00539878	frameshift-variant, intron-variant, utr-variant-3-prime	NEB, RIF1	GRCh38.p7	2:151497656	TTGATTGTGTTTGAC[-/TCTT]TCCATCTCGGGAGTG	4703
rs747575539	snp	C/T	1.65877e-05	0.00287986	missense	NEB	GRCh38.p7	2:151658080	TCTTCCAAGGAAAGT[C/T]TGTAGAGTTTCTGTA	4703
rs747576289	snp	A/T	3.31268e-05	0.00406968	missense	NEB	GRCh38.p7	2:151687470	CATCTTTGGATCGTC[A/T]TTAATGCTGAGGGCT	4703
rs747601206	snp	A/G	1.65605e-05	0.0028775	synonymous-codon	NEB	GRCh38.p7	2:151666213	CTGAGATTTCTTTGC[A/G]GCTGTCACACTGACC	4703
rs747601238	snp	G/T	0.000184111	0.00959279	intron-variant	NEB	GRCh38.p7	2:151592017	CTGTGAAAAGCAAAT[G/T]ATGTGCGCTGTCTTA	4703
rs747602368	in-del	-/AGA	1.92556e-05	0.00310281	intron-variant	NEB	GRCh38.p7	2:151537242	TATATTTTACCTGGG[-/AGA]AGAAGAACATCAAAG	4703
rs747602429	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151667705	GCTAATTTTTTTTTT[A/T]ATTTCTGTAGAGACA	4703
rs747606224	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151522169	ATTATATTTTTAGGA[A/G]TTTAATTGTATTTGA	4703
rs747606446	snp	C/T	1.65773e-05	0.00287895	synonymous-codon	NEB	GRCh38.p7	2:151655832	CTTGTTCATGGTATG[C/T]GCATTCTGCTTGGCA	4703
rs747618627	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151558406	CTATGCTCATGGATA[C/G]GAAGACTCAATATCG	4703
rs747654975	snp	A/C	6.06888e-05	0.00550824	intron-variant	NEB	GRCh38.p7	2:151646124	ATGCTGAATTTGAAA[A/C]CTTACATCACTTGTG	4703
rs747656491	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151539745	CCTCGATTGTGTGAT[A/G]TGGAAAATGAACATC	4703
rs747662624	snp	C/T	1.9975e-05	0.00316024	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151526235	GGCAGGTTCCTCTTT[C/T]CTTGACATGTTTCTC	4703
rs747662736	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151634598	AGTGACCCAAAATTA[C/T]GCCACTGCACTCCAG	4703
rs747673035	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151731647	GTAGGGATGGGATGT[C/T]TAAAAATAGCCACCT	4703
rs747680799	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151730377	AGGTCATCATGGCCT[G/T]CATGATGGATCTGCA	4703
rs747680930	snp	A/G	4.89548e-05	0.00494722	intron-variant	NEB, RIF1	GRCh38.p7	2:151496375	GTATAACACCTGTGC[A/G]ATGAGAAAGCATCCA	4703
rs747689558	in-del	-/AG	6.62076e-05	0.00575321	intron-variant	NEB	GRCh38.p7	2:151546007	ATTAGACTTAAAAAA[-/AG]AAAAAAAAAAACAGA	4703
rs747691417	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151669216	CCTTTAAAACGGAAG[C/G]CTATCATTTGTGTTT	4703
rs747692792	in-del	-/GG			intron-variant	NEB	GRCh38.p7	2:151707525	CAAGTAGGAGGAGGA[-/GG]ATGGAGCAGGGAGAA	4703
rs747695048	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151620025	ATGAAGAGTCCAATT[A/G]CAGTAATAAACCATG	4703
rs747695332	snp	A/G			missense	NEB	GRCh38.p7	2:151684905	GATTTCTTAGCTTGA[A/G]TGACTTGGAGCATAT	4703
rs747699601	snp	A/G	5.56344e-05	0.00527391	missense	NEB	GRCh38.p7	2:151568679	CTGTCATCCACAGGC[A/G]TAAAGTTGAGAGTTT	4703
rs747707574	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151617597	AAATTATTAAAGCTG[C/T]ATAAATTCCTTACCT	4703
rs747709979	snp	C/T	1.65603e-05	0.00287747	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151627694	GAACTTGGTCTTCCA[C/T]TTCTCAAAGTCCTTC	4703
rs747721528	snp	C/T	1.66092e-05	0.00288172	intron-variant	NEB	GRCh38.p7	2:151692234	GGAAAGCCCTCCTAC[C/T]CGAAAGGTAACCGTG	4703
rs747721713	snp	C/T	3.31406e-05	0.00407053	missense	NEB	GRCh38.p7	2:151672458	ATGGCTGTTTGTAGT[C/T]GACATTGGTAGCGAC	4703
rs747725529	snp	A/G	0.000105669	0.00726797	intron-variant	NEB	GRCh38.p7	2:151610881	GCTACAGGGCAGGGC[A/G]GCATGGGGCATGGGG	4703
rs747729019	snp	C/T	1.65721e-05	0.0028785	missense	NEB	GRCh38.p7	2:151656386	CTTGCATGGAATGGA[C/T]TAATTTGGGATCATC	4703
rs747736112	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151494994	GCAGCACTTAAACTC[C/T]CATAGACATATCAGT	4703
rs747738880	snp	C/G	1.74379e-05	0.00295273	intron-variant	NEB	GRCh38.p7	2:151697653	TTGTATAGTTTCTGT[C/G]AAAGAAAAAAAATTC	4703
rs747742809	snp	A/G	4.99297e-05	0.00499623	missense, intron-variant	NEB	GRCh38.p7	2:151619723	CTCGGGCGCCAATGT[A/G]GTGACCCAACTGTTT	4703
rs747743998	snp	C/T			missense	NEB	GRCh38.p7	2:151540738	TAGCATGCTTCAAGG[C/T]TGTGGTCTGGTTTCC	4703
rs747745090	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151496045	GAGAAGCAAAAGGAT[A/G]TTTTATAGGAAAATC	4703
rs747751758	snp	C/T	1.67801e-05	0.00289651	missense	NEB	GRCh38.p7	2:151553865	TTCCTGACGTGATCA[C/T]TGACTTGCAAGTCGG	4703
rs747759738	snp	A/G	6.913e-05	0.00587879	intron-variant	NEB	GRCh38.p7	2:151646253	AAATAAGAAATAATA[A/G]TTTTTCAGTGGTGTT	4703
rs747780924	in-del	-/TAACTA			intron-variant	NEB	GRCh38.p7	2:151535043	AATTAAATACAACTT[-/TAACTA]TAAAACCATCCCAAC	4703
rs747809024	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151707261	GCTTGGGGACAGATA[C/T]AAGAAAGAACACATG	4703
rs747809567	snp	A/G	3.31664e-05	0.00407211	intron-variant	NEB, RIF1	GRCh38.p7	2:151513555	CTACTTTCCTGAAAG[A/G]TTGACATCGAATAGT	4703
rs747822944	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151661274	AGATTTAAATCTTAA[A/G]AGAGGCACAGAAATT	4703
rs747837704	snp	C/T	0.0419388	0.138602	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151594154	TGACATCATGTCCAA[C/T]GGTGTGTTGTGAATT	4703
rs747847680	snp	C/T	1.65754e-05	0.00287879	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151609968	CACTGGGCTAGAGAA[C/T]TTGGTTTTCCACTTT	4703
rs747850462	snp	C/T	1.94007e-05	0.00311448	intron-variant	NEB	GRCh38.p7	2:151642760	ACTATGAATATATTA[C/T]TTACCTCACTGTAAT	4703
rs747860562	snp	C/G/T	3.32786e-05	0.00407902	intron-variant	NEB	GRCh38.p7	2:151546469	AACACAGAAATATAG[C/G/T]TGGTCATAAGCAAAT	4703
rs747863168	snp	G/T	1.77546e-05	0.00297943	missense	NEB	GRCh38.p7	2:151570356	GGGTGCCCACGTAGT[G/T]TCCCTTCTGCTTCTC	4703
rs747873337	snp	C/T	3.32552e-05	0.00407756	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151503349	TATATTTGTAAATAC[C/T]GAGCTAAAGTTCTCT	4703
rs747874307	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151514681	TAATAGATTAGGTGG[C/T]AGTACCAAGCACATG	4703
rs747898598	snp	C/T	6.62767e-05	0.00575621	missense, intron-variant	NEB	GRCh38.p7	2:151614535	TCATCCTTAATGTTC[C/T]GGGCCCCAATATGGT	4703
rs747905292	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151688702	TGATAAAGTTTAATT[C/T]ATATATTAGGCACAG	4703
rs747919357	snp	A/T	1.6566e-05	0.00287797	missense	NEB	GRCh38.p7	2:151553937	TCACTGACTTTCTTC[A/T]GGGAATCCTTGGCAG	4703
rs747922248	snp	A/G	1.91155e-05	0.0030915	intron-variant	NEB	GRCh38.p7	2:151727659	ATTTCTTAATAATCA[A/G]GCCAGGTTAGCAGAA	4703
rs747924696	snp	A/T	1.67922e-05	0.00289755	missense	NEB	GRCh38.p7	2:151675386	TCCTTTAGCCTTGTA[A/T]AAGATCTGCAATAAA	4703
rs747924748	snp	C/T	1.65721e-05	0.0028785	missense	NEB	GRCh38.p7	2:151671045	AGCTGCTTTGTGTTA[C/T]GCTGAGCCAACACCA	4703
rs747925018	snp	C/T	1.79693e-05	0.00299739	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151531017	CTTCATCTTTAACCT[C/T]GCGGACATGCAGCAA	4703
rs747928192	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151674111	CATTTTATATAACAT[C/G]TTTTCAATCTTTTTA	4703
rs747929421	snp	A/G	1.73622e-05	0.00294632	intron-variant	NEB	GRCh38.p7	2:151656480	CTGTGAAGAAAATAT[A/G]AGTTTTTACACAGAG	4703
rs747931478	in-del	-/GT	6.08958e-05	0.00551762	intron-variant	NEB, RIF1	GRCh38.p7	2:151491804	CAGTGATCAGAACAA[-/GT]GTTCTTGGAGTTTTC	4703
rs747932217	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151529122	AATCACTAGAGCTGA[A/G]TTGCCTGAAGAGATG	4703
rs747935845	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151705908	TGATATAATGGACTT[C/T]GGGGACTTGAGTGGA	4703
rs747936582	snp	C/T	0.000133398	0.00816585	intron-variant	NEB	GRCh38.p7	2:151548272	CCATGGCTATTGAAA[C/T]TCAATATGTCTCTTG	4703
rs747939711	snp	A/C	1.68371e-05	0.00290143	intron-variant	NEB	GRCh38.p7	2:151675261	GTCAGGTCCGAATTT[A/C]ACATCCCAGCAAAGA	4703
rs747942612	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151724799	TTTCTCCTATAAGAC[A/G]ATGCAGAGGTGATGC	4703
rs747946275	snp	C/T	2.10444e-05	0.00324373	splice-donor-variant	NEB	GRCh38.p7	2:151570496	AAAAAAGGCCACTCA[C/T]GTCACTGGCAATCTC	4703
rs747949097	snp	A/T	3.38558e-05	0.00411422	intron-variant	NEB	GRCh38.p7	2:151690836	GTATGCTAGAAAAGA[A/T]GATGTTCTTTAATGA	4703
rs747952544	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151717545	TAAAAGACAGGGATG[C/T]ATTTTAAAAACGATT	4703
rs747960478	snp	G/T			missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151502845	ATCTCTGGAGTGATA[G/T]GTGTTGGGATTCCTT	4703
rs747981393	in-del	-/G/GAGAG	0.000182983	0.00956336	intron-variant	NEB	GRCh38.p7	2:151617504	AGAGAGAGAGAGAGA[-/G/GAGAG]AAAATTATTTTGGTG	4703
rs747988039	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151641997	GGCCCCAGTGTGTGA[C/T]GTTCCCCACCCTGTG	4703
rs748004807	snp	A/T	2.94633e-05	0.00383807	intron-variant	NEB	GRCh38.p7	2:151620910	TGTTAGGACTTGATC[A/T]GCTCTTACATCACTG	4703
rs748015381	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151676949	CATTAAATAAATAAA[C/T]GAGTGAATGCTTTTG	4703
rs748018769	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151675544	AAAACAAGCATCTTA[A/T]TATCTTTAATACCAA	4703
rs748020383	snp	A/G	5.73345e-05	0.00535387	synonymous-codon	NEB	GRCh38.p7	2:151690730	CAAAGCACTTACATC[A/G]CTAAGCTGTTTCGTG	4703
rs748029822	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151549054	CAGTTGAGTACTTGT[A/G]AAAAGTGGAGAAGGG	4703
rs748032411	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151723138	CACTAACTAATGTGA[A/C]CCCAGATTCAGGTTT	4703
rs748036402	snp	C/T	1.65625e-05	0.00287766	missense, intron-variant	NEB	GRCh38.p7	2:151631240	GGCTGGCGGTAGATG[C/T]TATCACTCAGTATTT	4703
rs748037366	snp	A/G	1.91141e-05	0.00309139	missense	NEB	GRCh38.p7	2:151560647	GACAAGGTGCTGGAA[A/G]GCAGGATGTAGCTGG	4703
rs748045252	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151515744	GTATAAGAAACTCCT[A/G]TAGATCCTTTACTCA	4703
rs748048179	snp	G/T	3.59305e-05	0.00423839	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151490408	CCCCGTCGCTGTAAG[G/T]CGAAAGGTGGTGGTC	4703
rs748055566	snp	A/G	1.65658e-05	0.00287795	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151627109	AGATGTTATCACTCA[A/G]TATTTCAGCAGCTCT	4703
rs748060415	snp	C/T			upstream-variant-2KB	NEB	GRCh38.p7	2:151735909	ACTTACTAGTCATTA[C/T]ATGCTTTAAAATGTG	4703
rs748063124	snp	C/T	2.79279e-05	0.00373673	intron-variant	NEB	GRCh38.p7	2:151682813	CTTTGCTGTGTCATC[C/T]TCATTATGTAAAATC	4703
rs748065575	snp	A/C/G	3.32448e-05	0.00407695	intron-variant	NEB	GRCh38.p7	2:151541567	CTAGACATAAACCAA[A/C/G]TTATCACCATCATTT	4703
rs748066063	snp	A/C	3.31208e-05	0.00406931	missense, intron-variant	NEB	GRCh38.p7	2:151644052	ATGCATGGACCACAT[A/C]ATCTTGGGGTCATCT	4703
rs748079134	in-del	-/AAGA	1.67657e-05	0.00289527	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151506292	ACAGTGTTAACACAG[-/AAGA]AAGAAAAGAAAACCC	4703
rs748084943	snp	C/T	1.65778e-05	0.002879	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151525238	GGAGTAGTTGGATTT[C/T]CCTTTCTCCTTGACA	4703
rs748088676	snp	A/G	1.65625e-05	0.00287766	missense	NEB	GRCh38.p7	2:151563664	GGGAATTCACCGATC[A/G]CTTTTCCAGCCAGGT	4703
rs748089645	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151676791	CTGGATGACAATGCT[C/T]TGTTTGTAGCCATGT	4703
rs748099183	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151663472	CTTTCAGGATTTTCA[A/G]AACGTCATTGCTTAT	4703
rs748105415	snp	A/C	1.66181e-05	0.00288249	synonymous-codon	NEB	GRCh38.p7	2:151541489	GGCTCTTAAAAGATC[A/C]GGAGTATCAGGAACT	4703
rs748107385	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151664166	GAAAAGGCTGCAGGC[A/G]GGATTTCTCATGGTG	4703
rs748119905	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151487955	CGAATATGATACAAT[A/G]TGATATTTGATTCAA	4703
rs748120166	snp	A/G	3.32817e-05	0.00407919	missense, intron-variant	NEB	GRCh38.p7	2:151639912	TCCAGAGAGTCAGTC[A/G]CACTGGTAAATTTGA	4703
rs748121656	snp	A/G	0.000132512	0.00813869	missense	NEB	GRCh38.p7	2:151671115	CTGGGTGCTGTCGAT[A/G]CTTCCTCTCATTTAA	4703
rs748122258	snp	A/G	1.65608e-05	0.00287752	missense, intron-variant	NEB	GRCh38.p7	2:151631195	TGCTCTAGAGAATCA[A/G]TCACACTGGTAAATT	4703
rs748123049	snp	C/T	0.000223278	0.0105636	intron-variant	NEB	GRCh38.p7	2:151650909	AGAGAAAACACAGCT[C/T]TTTTAGTACACAAAG	4703
rs748133379	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151503951	GAGATGGCTTAATCA[A/G]TTTATTTTTCAGGAA	4703
rs748136244	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151696351	TTTGGCCACCCAGAC[A/T]TCAATGACAGAGCTA	4703
rs748140650	in-del	-/AATG	1.65332e-05	0.00287512	frameshift-variant, intron-variant	NEB	GRCh38.p7	2:151631247	GTAGATGTTATCACT[-/AATG]CAGTATTTCGGTAGC	4703
rs748144272	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151536264	CAGTAAAGGGTAGAA[C/T]TGCCTAGATGTCTTG	4703
rs748144877	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151577870	AGGTGTGAGCCACAG[C/T]GCCCAGCCTATGTCA	4703
rs748146504	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151564216	CTGGAGTGCAGTGCC[A/G]TGATCTAAGCTCACT	4703
rs748163166	in-del	-/AAA			intron-variant	NEB	GRCh38.p7	2:151628902	AAACAAAAACAAAAG[-/AAA]AGAAGAAGAAGAAGA	4703
rs748167683	snp	C/T	1.69137e-05	0.00290802	missense	NEB	GRCh38.p7	2:151665341	TCCTTACCTTGTCCA[C/T]GTTCAGTTTGTTACT	4703
rs748169663	snp	A/G	0.000388048	0.0139238	synonymous-codon, intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151499304	TTTAAATACCGAACT[A/G]AAGTTTTCTTGATTG	4703
rs748173187	snp	C/T	1.74163e-05	0.00295091	missense	NEB	GRCh38.p7	2:151570188	TGTCACTGACCAGAG[C/T]CTGGGAATTTTTAGA	4703
rs748182149	in-del	-/CT			intron-variant	NEB, RIF1	GRCh38.p7	2:151505946	TACCTTCTCACAAGC[-/CT]CTCTGTTTTTCAGAT	4703
rs748186692	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151715199	ATGCAAGTCATTCTT[C/G]TAGCCACATTTTTAA	4703
rs748186794	snp	A/G			missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151490489	CACTGGCAGATCGTG[A/G]CTGCTCCCGGCTCCG	4703
rs748203894	snp	G/T	1.726e-05	0.00293763	intron-variant	NEB	GRCh38.p7	2:151662378	ATTATGAGAAGAAAC[G/T]GGAACTTCCCAAGAA	4703
rs748209108	snp	C/G	1.90871e-05	0.0030892	intron-variant	NEB	GRCh38.p7	2:151688259	CTCTTTTCATGTACA[C/G]CAAACATAGGCTTCT	4703
rs748221928	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151683349	GGTTATTATTTGGAA[C/T]TGGTCCTAGTTGAGG	4703
rs748226247	snp	C/T	0.00433837	0.046372	missense, intron-variant	NEB	GRCh38.p7	2:151583724	GGGTGCGGAAACCCA[C/T]GTGGTGGCCCAGTTG	4703
rs748228489	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151569782	GTCCATGGGCTGCCA[A/G]TATTTTACTGGATAT	4703
rs748228984	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151694831	CTTCTCTACTCCCCA[C/T]GAGAATTTTTTATCA	4703
rs748230801	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151616877	TGTGGACTATTATCT[C/T]GGACAATGATTCATA	4703
rs748230949	snp	G/T	1.81869e-05	0.00301548	intron-variant	NEB	GRCh38.p7	2:151567131	TCTCAGAGTGTACCA[G/T]GCGTTTCTAGATAAT	4703
rs748239538	snp	A/G	3.31225e-05	0.00406941	missense	NEB	GRCh38.p7	2:151694393	ATGCTGAGGACTCCA[A/G]TCATTTTCCCTTTGT	4703
rs748242961	snp	G/T	1.67019e-05	0.00288975	missense	NEB	GRCh38.p7	2:151672664	TTTGACTTCTCATAA[G/T]CTTCCTTGTATTTAT	4703
rs748242988	snp	C/T	1.65564e-05	0.00287714	intron-variant	NEB	GRCh38.p7	2:151679677	CCCCAAGCCCACCCA[C/T]CCACATTTTCTAGTT	4703
rs748243107	snp	A/G/T	5.26185e-05	0.00512903	missense, synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151619463	TACGTCACTCTGGAG[A/G/T]TCATAGGCTTTCCGT	4703
rs748244283	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151649587	GTTGAGTAATCTTTC[C/G]CTTCTTTGCATATAA	4703
rs748246603	snp	A/G	1.65669e-05	0.00287805	synonymous-codon	NEB	GRCh38.p7	2:151694332	ACTCACATCACTCTG[A/G]TTTTTGGCCACCTTC	4703
rs748254970	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151555259	AATCAGACTGTATCA[A/C]AAGTACTTTTAAACC	4703
rs748268365	snp	A/G	1.74315e-05	0.00295219	intron-variant	NEB	GRCh38.p7	2:151633999	AATCAGGTTTTTATT[A/G]TAACCCCTTAGAGGC	4703
rs748269558	snp	A/C	1.67567e-05	0.00289449	missense	NEB	GRCh38.p7	2:151537193	GTATCATAGGCATAG[A/C]AACCAATGCCTTTAA	4703
rs748282591	in-del	-/C	5.10356e-05	0.00505126	intron-variant	NEB	GRCh38.p7	2:151567524	GTTTTGACAAGCACA[-/C]CAAGGCAGAGGGGGC	4703
rs748289685	snp	C/T	3.64618e-05	0.00426961	intron-variant	NEB	GRCh38.p7	2:151609787	TTCCCCTTCCCCCTT[C/T]CCCAAAATTCATGTT	4703
rs748290377	snp	A/G	2.26904e-05	0.00336819	intron-variant	NEB, RIF1	GRCh38.p7	2:151527474	GTCTGTGTCTCTCCT[A/G]TCTTACATCGCTTTG	4703
rs748298265	snp	A/G	6.4539e-05	0.00568026	intron-variant, utr-variant-3-prime	NEB, RIF1	GRCh38.p7	2:151497733	CCTGTGCGATAAGAA[A/G]GCATCCAGAAAAACA	4703
rs748303993	snp	C/G	1.65701e-05	0.00287833	missense	NEB	GRCh38.p7	2:151725484	TGTACTTTTTTGATT[C/G]TGCGAAGTTCTGGAG	4703
rs748306872	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151697009	CAAGGGAAAATAGGA[C/T]GTTTACTACAAAATA	4703
rs748311158	snp	C/T	2.83579e-05	0.00376539	missense	NEB	GRCh38.p7	2:151570095	CATCGCTCTGCAGTT[C/T]GTAGGCCTTCTTGGC	4703
rs748311856	snp	A/C	1.65614e-05	0.00287757	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151524544	TGGCTGCCTGTGTGG[A/C]CTTCTTGATGTCTGG	4703
rs748314709	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151668969	CAGAGCAAGAGTTGC[A/G]AAGAACCAGAAAGGA	4703
rs748315043	snp	C/G	2.36119e-05	0.0034359	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151508065	GGTGTCCAAAACAGT[C/G]TCATAATACGACATG	4703
rs748318479	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151571609	AATGTTAGATCTTCC[A/G]CTGAAGCATGATTGG	4703
rs748325862	snp	A/G	3.31362e-05	0.00407026	missense	NEB	GRCh38.p7	2:151680743	ACATCACTCCTCTGG[A/G]CCTGGTTAATTTTAG	4703
rs748332134	snp	C/T	1.71023e-05	0.00292419	synonymous-codon	NEB	GRCh38.p7	2:151688379	CTTCTCACCTTCATG[C/T]TTTGCTTTGTAATTC	4703
rs748339284	snp	A/G	8.87403e-05	0.0066605	synonymous-codon	NEB	GRCh38.p7	2:151562740	CCTTTTAGCCAGCAC[A/G]TGATTCATCATGTCA	4703
rs748349518	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151641622	AGGTGTGAGCCATGG[C/T]GCCTGACCTATACAC	4703
rs748357667	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151643399	TTAAATCATTTATCA[C/T]AATTTGTCATAATTT	4703
rs748358450	in-del	-/GACT			frameshift-variant	NEB	GRCh38.p7	2:151567297	CTGCTTGGCGGCCAA[-/GACT]GACACCATATCAGCA	4703
rs748358612	snp	A/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151494016	AAATAGTTAATGGCT[A/T]CAGTAAATGTAGTGT	4703
rs748359305	snp	C/T	1.78121e-05	0.00298425	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151650586	GACCTCACTTTGCAG[C/T]TCATAAACTTTCTTA	4703
rs748363300	snp	A/G	1.91459e-05	0.00309396	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151527550	AGTCCACTTCCAGTG[A/G]GCTTTGTTGGCTTCG	4703
rs748368046	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151651480	TTTGCCATGTGGTTA[C/T]GTCATATAACCTTGT	4703
rs748370445	snp	A/G	4.97022e-05	0.00498484	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151614360	ATGCAGGGGATGCTT[A/G]TAGTCTATGTCGCTT	4703
rs748373113	snp	G/T	1.95789e-05	0.00312875	intron-variant	NEB	GRCh38.p7	2:151547596	ATTAACATTCATCCC[G/T]AGTCTCTACTCCCTG	4703
rs748386134	snp	A/C			intron-variant	NEB, RIF1	GRCh38.p7	2:151510264	TAGACCCACAGTAAA[A/C]CTTGTTTAATTCTAC	4703
rs748386782	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151703911	CTGGTGAGGAACTGC[A/G]TTCCTTTGGAGGAGG	4703
rs748388746	snp	C/T	0.000166246	0.00911568	intron-variant	NEB	GRCh38.p7	2:151709649	AAATGGGATGATTTC[C/T]TCATACCTTGCTAGC	4703
rs748392411	snp	G/T	1.6574e-05	0.00287867	missense	NEB	GRCh38.p7	2:151567266	GATAATCAATATCAC[G/T]GACAAGGGTCTGCCC	4703
rs748395516	snp	A/G	0.000272257	0.0116642	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151636275	CACGATGGGGATGGC[A/G]TCGCTTCGCAAGTCA	4703
rs748402585	snp	A/G	1.66877e-05	0.00288852	intron-variant	NEB, RIF1	GRCh38.p7	2:151492507	AACCTGATGCAGGAG[A/G]GACCGTGAATGAGTG	4703
rs748407608	snp	G/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151486002	AACACACATCTATTT[G/T]TAAGATCTCTCATGA	4703
rs748408038	snp	C/G	1.8517e-05	0.00304272	missense	NEB	GRCh38.p7	2:151664805	AGTAAAATATCCGGT[C/G]TGTCAGGCATGACAT	4703
rs748409064	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151524792	CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGGACTG	4703
rs748415881	snp	A/G	1.65616e-05	0.00287759	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151524401	TTCCTTGCGGTGCTT[A/G]GCTCTGTACTCCACC	4703
rs748423678	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151637527	ACATCAGAGGGGAGC[A/G]CCCATGGCAGCGTCC	4703
rs748427401	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151556745	CAGAGAGACTTAGAA[G/T]GCAACACAATAATAG	4703
rs748447261	snp	C/T	1.66045e-05	0.00288132	missense, intron-variant	NEB	GRCh38.p7	2:151650369	CACTCAAGGTCAGAT[C/T]TATATAGATTCTGTG	4703
rs748448253	snp	C/T	1.65979e-05	0.00288074	missense	NEB	GRCh38.p7	2:151576209	GGTGTGTCAACAATG[C/T]TTGTGTACTTAAGGT	4703
rs748453057	snp	A/T	1.65616e-05	0.00287759	stop-gained	NEB	GRCh38.p7	2:151677738	TCCAGCCAATGCCTT[A/T]CATCCAGTTGTTGTA	4703
rs748458332	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151624250	AAAGCCTTCAATGCA[G/T]GATCATGCAATTTTA	4703
rs748458556	snp	A/G	3.31422e-05	0.00407063	synonymous-codon	NEB	GRCh38.p7	2:151659097	CATTTGCCTTTGCCA[A/G]AATAATCTGGGGGAT	4703
rs748460393	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151567668	ACCCATTTAAAAATA[G/T]AAAAATATTCTGCTG	4703
rs748461742	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151671403	AGAAGCTGTTCTGTT[A/G]TTAGAGTGCATTATA	4703
rs748475168	snp	C/T	1.65655e-05	0.00287793	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151505566	ATTGCTTCCTTATAC[C/T]TCACCTGCAGATTTA	4703
rs748478190	snp	A/T			intron-variant, utr-variant-3-prime, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151498132	AAATGGGAAAGTATA[A/T]CCTTTTGTAATATAA	4703
rs748478191	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151511841	TTGAGATTGGTAATC[C/T]AAATGTGGGCTACTT	4703
rs748479655	snp	A/G	0.000369788	0.0135925	synonymous-codon	NEB	GRCh38.p7	2:151669090	TTCAGGGTCAATAGT[A/G]TACTTGTGCTTCAGT	4703
rs748482247	snp	C/T	1.65693e-05	0.00287826	missense, intron-variant	NEB	GRCh38.p7	2:151643849	TAGGCCTGCCGAGCA[C/T]GGATGACATCGCTCT	4703
rs748500096	snp	C/T	1.67922e-05	0.00289755	intron-variant	NEB	GRCh38.p7	2:151710392	CTAAGGAAAGGGGTC[C/T]CCCTCCCAGGATGAC	4703
rs748500508	snp	C/T	3.32121e-05	0.00407492	intron-variant	NEB	GRCh38.p7	2:151563556	AACAGGCAGACACGG[C/T]AGCACACTTATGGGG	4703
rs748513829	snp	C/T			missense, intron-variant	NEB	GRCh38.p7	2:151625541	GATCTTACCTCACTA[C/T]AATTTATTTTATTTT	4703
rs748515593	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151544291	TAAAGGTATTTCAGA[A/G]TTATCTTTACTCTGA	4703
rs748518353	snp	C/T	3.28305e-05	0.00405144	missense	NEB	GRCh38.p7	2:151709697	TATTCATTTTATACT[C/T]TGGTGTTTCGGTCTG	4703
rs748523874	snp	C/G	1.65627e-05	0.00287769	synonymous-codon	NEB	GRCh38.p7	2:151680817	GGTGTCTGGATGTTG[C/G]CGATATTTTTTCTGT	4703
rs748525509	snp	C/G/T	3.31352e-05	0.00407022	missense, synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151490043	TGAAGATGATCGTTG[C/G/T]TGTGGGAGCTCTGTG	4703
rs748541129	snp	C/T	1.68117e-05	0.00289923	synonymous-codon	NEB	GRCh38.p7	2:151551744	ACTGCTCACCGAACT[C/T]TGGAGCTTGTATGCA	4703
rs748547529	in-del	-/A			intron-variant	NEB	GRCh38.p7	2:151670404	CATTGTAATTCGCTT[-/A]CTGACAGAAAGAATA	4703
rs748550315	in-del	-/TGAG	9.07565e-05	0.00673572	frameshift-variant, intron-variant	NEB, RIF1	GRCh38.p7	2:151501410	TAAAGTTTTCTTGAT[-/TGAG]TGAGTTTGACTCGCT	4703
rs748552068	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151536702	TTGCTGGATCCTATT[A/G]TACAACCCAAATGCA	4703
rs748557105	snp	G/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151526744	TGGCCCTTGCACTGC[G/T]GCTGCCCTGCTTGAC	4703
rs748557938	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151658546	TTCAAACAAAGAAAT[G/T]ATAAAAATAGGATTA	4703
rs748559658	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151672191	ATAATTATGATATAA[A/G]CACAGAAAGCAGGCA	4703
rs748559932	snp	A/G	1.80091e-05	0.0030007	intron-variant	NEB	GRCh38.p7	2:151696609	TATCCCTCATAATTG[A/G]GTGTCCTGAGTAGTT	4703
rs748561855	snp	A/C/G	3.40346e-05	0.00412509	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151493376	TGTTTTCTTGGTTGC[A/C/G]CTTAGCTCTCTCCAT	4703
rs748564316	snp	C/T	1.65924e-05	0.00288027	missense	NEB	GRCh38.p7	2:151540776	TGATGGGGTCTCTCT[C/T]TGGTGGCAAGTTCAA	4703
rs748570482	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151642205	CTATAATTCAGCCCT[C/T]GTAGATTCATTGGTT	4703
rs748570945	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151530554	GTTTACCAATTTACT[C/T]ATCAGTATCTTTAGG	4703
rs748573296	snp	C/T	1.6617e-05	0.00288239	intron-variant	NEB	GRCh38.p7	2:151575849	ACAATTTTCATGTTG[C/T]TAGTCCCACTATGCA	4703
rs748581626	snp	A/G	1.65534e-05	0.00287688	intron-variant	NEB	GRCh38.p7	2:151618233	TTTTTAAATTGTTCT[A/G]TGGTAACTTTCGGTA	4703
rs748591900	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151486553	TAATTTGTACATCCA[C/T]GTCCGTAGCAGCATT	4703
rs748594782	snp	C/T	6.62526e-05	0.00575516	missense	NEB	GRCh38.p7	2:151692117	GGGTCCTCCATGCTG[C/T]CTACATAATGTCCCA	4703
rs748600035	snp	A/C/T	3.31599e-05	0.00407174	missense, intron-variant	NEB	GRCh38.p7	2:151633697	GCATGGATGACATCG[A/C/T]TCTGGTCAGGCAGGC	4703
rs748607410	snp	C/G	3.40768e-05	0.00412762	missense, intron-variant	NEB	GRCh38.p7	2:151609859	TAATGTCGTTTTGAT[C/G]CGGCATGCATGTCCA	4703
rs748618562	snp	A/G	1.65707e-05	0.00287838	missense, intron-variant	NEB	GRCh38.p7	2:151640381	GGTCATAGGCCTGCC[A/G]AGCATGGATGACGTC	4703
rs748634386	snp	A/G	2.0723e-05	0.00321886	intron-variant	NEB	GRCh38.p7	2:151655387	ATGCTAGGAAGTGGG[A/G]AAAAAAGACATGAAA	4703
rs748634452	snp	A/C	1.65701e-05	0.00287833	intron-variant	NEB, RIF1	GRCh38.p7	2:151506134	TCAAAGGGAGGCAGA[A/C]AATATTGCAAGTGCA	4703
rs748649959	snp	C/G	3.33918e-05	0.00408592	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151526174	TCAGACACCAGGTTG[C/G]TGACAGTCTTCGCCA	4703
rs748661428	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151614798	AGCAGGTGGCAGCAT[A/G]AGCCTAGAATGAAGA	4703
rs748666706	snp	C/T	0.000124821	0.00789903	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151496287	GTACCGAGCTAATAT[C/T]TTCTTGATTGTGTTT	4703
rs748667515	snp	A/T	1.66142e-05	0.00288216	missense	NEB	GRCh38.p7	2:151555043	TCTTCCCGATATTTG[A/T]TCTATAGAGAATAAG	4703
rs748679499	snp	A/T	3.31549e-05	0.0040714	missense	NEB	GRCh38.p7	2:151729646	TCGTAAACCACTTCT[A/T]CTGTGTAGTACTGTA	4703
rs748684538	snp	G/T	1.66194e-05	0.00288261	missense	NEB	GRCh38.p7	2:151696661	TTGTTTGGAATTGAC[G/T]TGGGCTTGTAGCAGA	4703
rs748684620	snp	C/T	8.28535e-05	0.00643583	missense	NEB	GRCh38.p7	2:151692063	TTCAAACTTACATCA[C/T]TGTTTTGAGCTGCAA	4703
rs748691260	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151710963	TCCAGAAAGAAACAA[C/T]CACAATAAAATTCAA	4703
rs748704765	snp	A/C	3.3557e-05	0.00409602	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151534194	TCCTGCCTGGGCCAC[A/C]GGCCAGCCCCATCAC	4703
rs748724373	snp	A/C	1.68272e-05	0.00290057	intron-variant	NEB	GRCh38.p7	2:151659211	GTTTAAAATCTTAAA[A/C]GAAGCTCACTTAGTA	4703
rs748728868	snp	C/T	1.71146e-05	0.00292524	utr-variant-3-prime, intron-variant	NEB, RIF1	GRCh38.p7	2:151485759	TGATGCTTTGAAATG[C/T]CTAAATAGCTTCAAC	4703
rs748738174	snp	A/T	1.67697e-05	0.00289561	missense	NEB	GRCh38.p7	2:151677887	TTACATCACTCTGTA[A/T]CTGCATCATGTTCTT	4703
rs748741238	snp	C/G	1.6569e-05	0.00287824	missense	NEB	GRCh38.p7	2:151679934	TCACTGATATTGTAG[C/G]CATTAACTTTAGCCT	4703
rs748741696	snp	C/T	0.000294421	0.0121295	intron-variant	NEB	GRCh38.p7	2:151606558	AAAATAGTCTCCCTG[C/T]TCGTTTTGTAGAAAA	4703
rs748742142	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151611830	GAAGTGTAAATGGCT[C/T]ATATTCCTTACCAGA	4703
rs748759110	snp	A/G	3.33506e-05	0.0040834	intron-variant	NEB	GRCh38.p7	2:151642900	AAACATGACTGGTAT[A/G]GGCCAGTAATAAATA	4703
rs748760784	snp	G/T	1.65949e-05	0.00288048	missense	NEB	GRCh38.p7	2:151663753	TATTCCCGGTCTGAC[G/T]GCATCTTGGCCACTT	4703
rs748766619	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151670029	TTCCAGCTTGAGTAA[C/T]GAGGTAGATGTTGAT	4703
rs748770036	snp	A/G	1.6574e-05	0.00287867	synonymous-codon	NEB	GRCh38.p7	2:151538179	GCGATGATAGACAAT[A/G]TCTAGGGCATCTTTC	4703
rs748776713	in-del	-/A			intron-variant	NEB	GRCh38.p7	2:151575247	TTAATTTCTTGCTGT[-/A]TGTTTTTTGGTTTTT	4703
rs748780345	in-del	-/TA	1.71765e-05	0.00293052	intron-variant	NEB, RIF1	GRCh38.p7	2:151492326	ATATGATGGTGTGAC[-/TA]TATCCCTTTTTACAC	4703
rs748785523	snp	C/G	3.31873e-05	0.0040734	intron-variant	NEB	GRCh38.p7	2:151562236	GAAAGAGAGAACAAT[C/G]AAATGTGGAAGGTAT	4703
rs748799656	snp	C/G			missense, intron-variant	NEB	GRCh38.p7	2:151620935	TCACTGGCAATATCC[C/G]GAGAGGCCTTGGCAG	4703
rs748802423	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151708391	TCTTGTTCAGGTCAC[C/T]AGAGACCAGACATTG	4703
rs748806846	snp	A/T	1.67775e-05	0.00289629	missense, intron-variant	NEB	GRCh38.p7	2:151619736	GTGGTGACCCAACTG[A/T]TTACGATATGCTTCT	4703
rs748807974	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151611383	ATAGCAGATACTCAA[C/T]GATTTTTTGGTGATT	4703
rs748813339	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151623363	TCATCCCTCTACTTT[A/T]TACTGTTCAGTGTAC	4703
rs748823676	snp	C/G	3.3106e-05	0.0040684	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151513605	ATATCAGTAGCATTC[C/G]TGGCCCTCATAAAAT	4703
rs748829230	snp	A/C	6.59044e-05	0.00574002	intron-variant	NEB	GRCh38.p7	2:151690843	AGAAAAGAAGATGTT[A/C]TTTAATGAAATATCA	4703
rs748833645	in-del	-/TTG			intron-variant	NEB, RIF1	GRCh38.p7	2:151533888	ATTTTTGTTTGTTTT[-/TTG]TTGTTGTTTGTTTAT	4703
rs748838869	snp	C/G/T	0.000115838	0.00760973	intron-variant	NEB	GRCh38.p7	2:151697693	AGATTCCTGTCACTC[C/G/T]CACGCTGATTATAAC	4703
rs748841596	snp	C/T	5.1402e-05	0.00506935	intron-variant	NEB	GRCh38.p7	2:151621073	GAATTCACATTCACT[C/T]GAAAAGTATATTTTC	4703
rs748842079	snp	C/G	1.66062e-05	0.00288146	missense	NEB	GRCh38.p7	2:151663681	TTGGCTGCCACCACA[C/G]TGAGCATGTCCACCG	4703
rs748842263	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151576814	TGCTGGGATTACAGG[A/C]ATGAGCCACTACGCC	4703
rs748846666	in-del	-/T			intron-variant	NEB	GRCh38.p7	2:151644253	CCAAAGACTTCAGTC[-/T]TTTGATAAGAAAGAT	4703
rs748849840	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151577703	CCTGCCTCAGCCTCC[C/T]GTGTAGCTGGGATTA	4703
rs748864845	snp	A/T	1.65638e-05	0.00287778	missense	NEB	GRCh38.p7	2:151666309	CTGGATTTTGGCCAC[A/T]TTCATGTAGTGAACC	4703
rs748877908	in-del	-/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151515776	ATTGACCAATTGTTT[-/G]AAGCCATTTTAAAGT	4703
rs748878958	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151657063	CCAACTTTCTTCTAC[A/T]GAGGGGAGATCTTGA	4703
rs748879863	in-del	-/AAG			intron-variant	NEB	GRCh38.p7	2:151654252	AAAACAAGCTGTTTA[-/AAG]GAGGGGAAAAAGCAC	4703
rs748883194	snp	G/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151529202	TTGGGGAAGTTTCTG[G/T]AACTTACATTGGTGT	4703
rs748885286	snp	G/T	1.67809e-05	0.00289658	intron-variant	NEB	GRCh38.p7	2:151627868	TTTCAAAAATAAAAA[G/T]GAATAGAAAGGCTTA	4703
rs748890641	snp	C/T	1.65987e-05	0.00288082	missense, intron-variant	NEB	GRCh38.p7	2:151639925	TCACACTGGTAAATT[C/T]GAATCTGTCTGGAGG	4703
rs748900763	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151530356	CTTCCAGCTTCACCC[A/G]CTTTTGCTCTTCTTA	4703
rs748915406	snp	A/G	2.15209e-05	0.00328024	missense	NEB	GRCh38.p7	2:151658041	ATTGCATCAGGTCTG[A/G]GATCATAGCCTTTCT	4703
rs748918372	snp	C/G/T	5.43187e-05	0.00521123	intron-variant	NEB	GRCh38.p7	2:151615982	GAATAAGAAATGGCT[C/G/T]TTCCAAAACATCCAC	4703
rs748919494	snp	A/C	1.66087e-05	0.00288168	missense	NEB	GRCh38.p7	2:151727763	TGAAGGATCCACTTT[A/C]TTCCGGATGACCTTC	4703
rs748922882	snp	C/G	1.67072e-05	0.00289021	stop-gained, intron-variant	NEB, RIF1	GRCh38.p7	2:151525265	GACAAACTTCTTTTT[C/G]TAATTTGTCTAAATA	4703
rs748941455	snp	A/C/G	0.000217531	0.0104272	intron-variant	NEB	GRCh38.p7	2:151675413	TAAAATGCATTTCAC[A/C/G]TAGTGCAAAAAGGAA	4703
rs748949581	snp	A/G/T	3.3711e-05	0.00410543	intron-variant	NEB	GRCh38.p7	2:151663872	GTACTGTGGACAGAG[A/G/T]AGAAATTATGGTGAT	4703
rs748950090	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151516065	TTGATAAACATCTTG[A/G]TCACAAATACCCTTT	4703
rs748955611	snp	A/G	1.65614e-05	0.00287757	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151643213	ATCCATAAGGCTGGA[A/G]AACTTAAATTGATCT	4703
rs748965422	snp	C/G	1.90569e-05	0.00308676	intron-variant	NEB	GRCh38.p7	2:151695536	AAACATAAAAGCACA[C/G]GTTGTCAGTACATCA	4703
rs748974435	snp	C/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151490914	GTCTTTCTCTGTGTT[C/G]CCAAAATACCATGGG	4703
rs748975894	snp	C/T	1.76197e-05	0.00296809	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151531025	TTAACCTTGCGGACA[C/T]GCAGCAACATGGGTG	4703
rs748976723	in-del	-/TTA			intron-variant	NEB	GRCh38.p7	2:151634729	ACCGAGGAGAATTTA[-/TTA]TTATTATTATTATTT	4703
rs748977335	snp	C/T	1.65641e-05	0.00287781	missense	NEB	GRCh38.p7	2:151553971	CCATCTCTACCATGT[C/T]GGGCACGATGTGGAT	4703
rs748978197	snp	A/G	0.000153325	0.00875437	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151494221	AGTGACAGGGGTTGC[A/G]GTGGCTTTCCCCACA	4703
rs748982274	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151592001	GGTTAGGCAGAGAGC[A/G]CTGTGAAAAGCAAAT	4703
rs748987521	snp	C/T	5.96546e-05	0.00546111	missense, intron-variant	NEB	GRCh38.p7	2:151639865	GTCTCACCTTGTTCA[C/T]AGTGATGGCATTATT	4703
rs748989842	snp	A/G	5.94489e-05	0.00545169	intron-variant	NEB	GRCh38.p7	2:151568066	CTCCCATCAGGATGT[A/G]TTACCTCACTCTGAA	4703
rs748990736	snp	A/T	1.65723e-05	0.00287852	stop-gained, intron-variant	NEB, RIF1	GRCh38.p7	2:151518407	TACTCTTCTCATACT[A/T]CTTCTTGTACTGGTA	4703
rs749003938	snp	A/T	1.65663e-05	0.002878	stop-gained, intron-variant	NEB, RIF1	GRCh38.p7	2:151485823	CCTCTGCACAGTGCC[A/T]TACATCCAGCCTTCA	4703
rs749008823	snp	A/G	1.70197e-05	0.00291711	intron-variant	NEB	GRCh38.p7	2:151548460	TGATGGGTAAACAAG[A/G]ACCAACATTACATTT	4703
rs749009922	snp	A/C	1.66529e-05	0.00288551	intron-variant	NEB	GRCh38.p7	2:151538261	TAGAAAGAGAAAAAA[A/C]ACATGAATTACAAAA	4703
rs749015752	in-del	-/T	1.66178e-05	0.00288247	intron-variant	NEB	GRCh38.p7	2:151618257	TTCGGTATCTAACAG[-/T]GAGGATTGAAGACTC	4703
rs749021345	snp	C/T	1.71097e-05	0.00292481	missense	NEB	GRCh38.p7	2:151563828	TCATACTGACCTCAC[C/T]GTTCACCAGATCAGC	4703
rs749034995	snp	C/T	0.000109802	0.00740871	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151490497	GATCGTGACTGCTCC[C/T]GGCTCCGGCGCTGAG	4703
rs749035919	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151676901	CAGCAGGTAATACAG[C/T]GCCTGGCACATGGTA	4703
rs749040192	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151504072	TAGTATCTAAGGACT[A/G]TGCATTTTAATGAAA	4703
rs749042104	snp	C/T	1.67242e-05	0.00289168	missense, intron-variant	NEB	GRCh38.p7	2:151654042	GTACAGAAATTGCAT[C/T]AACTGGGAGATCATA	4703
rs749050869	snp	C/T	4.96882e-05	0.00498414	intron-variant	NEB, RIF1	GRCh38.p7	2:151524509	ACATTTTCATGACAC[C/T]CTTACCTCACTGGCC	4703
rs749054242	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151615605	GTAAGGAAGAGTTTA[C/T]ATGTATATTGGCTGT	4703
rs749055833	snp	A/G	1.65641e-05	0.00287781	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151629581	GGCAGCCACGATGGG[A/G]ATGGCGTCACTTCGC	4703
rs749056839	in-del	-/AA	0.000168172	0.00916829	intron-variant	NEB	GRCh38.p7	2:151633968	CTTTATATTTGTACT[-/AA]AATGAAAATGCACAA	4703
rs749058044	in-del	-/A	1.65913e-05	0.00288017	intron-variant	NEB	GRCh38.p7	2:151644458	ATATCAACAGAGGAT[-/A]AAATCTTACTTCACT	4703
rs749074172	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151549991	AGTAGTTCCTGGCCA[C/G]GTGTGGTAGCTGACA	4703
rs749076437	snp	C/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151490924	GTGTTCCCAAAATAC[C/G]ATGGGCAGACCTTTA	4703
rs749076925	snp	A/G	1.78918e-05	0.00299092	missense	NEB	GRCh38.p7	2:151684830	ACATTGATGCTATCA[A/G]GGGGGTAGCTGTAAC	4703
rs749082898	snp	A/G	1.65603e-05	0.00287747	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151525958	TGGTTGATCACTTAC[A/G]TCACTGACATGCTTG	4703
rs749091687	snp	A/C	2.99415e-05	0.00386909	intron-variant	NEB	GRCh38.p7	2:151682819	TGTGTCATCCTCATT[A/C]TGTAAAATCATCAAA	4703
rs749100154	snp	A/C	3.37718e-05	0.00410911	intron-variant	NEB, RIF1	GRCh38.p7	2:151503466	ATAATTAGAATACCC[A/C]GAAAGGTAAAATGAC	4703
rs749120253	snp	C/T	1.65847e-05	0.0028796	intron-variant	NEB	GRCh38.p7	2:151680725	TAGATAGCATTAACA[C/T]TTACATCACTCCTCT	4703
rs749120737	in-del	-/T			frameshift-variant	NEB	GRCh38.p7	2:151659084	CTCATATTAATTGCA[-/T]TTGCCTTTGCCAAAA	4703
rs749123729	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151630482	AGTGTCTAAAATACT[A/C]CTCAGTCCCACTGAC	4703
rs749125049	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151664342	ATGAACAGATGATTA[A/G]AGGGTACTTGGATGG	4703
rs749127170	in-del	-/A	0.00102866	0.0226555	intron-variant	NEB, RIF1	GRCh38.p7	2:151514958	AAGGAAAGACAAGTT[-/A]AAAAAAAATCTTTAT	4703
rs749127568	in-del	-/TTG			intron-variant	NEB, RIF1	GRCh38.p7	2:151501577	AAAGAAGTATTTTTA[-/TTG]TTGTTTTTATGATGA	4703
rs749128283	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151731370	TTAGAGTAGAGAGAA[C/G]AGTAAAACTTTATTT	4703
rs749128793	snp	C/T	8.99046e-05	0.00670405	missense	NEB	GRCh38.p7	2:151684882	CAACGTCGCTGGCAA[C/T]TGCCTGAGATTTCTT	4703
rs749132969	snp	G/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151505006	CACATGTCTACCCAG[G/T]GTCTTTTTGGACACT	4703
rs749148737	snp	A/G	5.86665e-05	0.0054157	intron-variant	NEB	GRCh38.p7	2:151610154	AGGTGGAGACATCCA[A/G]TTTTAAAACCATGCT	4703
rs749150490	snp	C/T	4.06438e-05	0.0045078	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151616089	CTTCTTGGACTCTTC[C/T]AAAGCAAGTTTATAG	4703
rs749151324	snp	A/G	5.67328e-05	0.00532571	intron-variant	NEB, RIF1	GRCh38.p7	2:151507956	GAGGCATCTTCCTCA[A/G]CACCCCTAGGTGCCT	4703
rs749153659	snp	A/G	3.39928e-05	0.00412253	missense	NEB	GRCh38.p7	2:151727881	GATGTCCTTGTTGTC[A/G]TAGTCTCATAAATTT	4703
rs749166661	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151715536	GGGAACCCCATAATG[A/G]GATTATCATCCTTAT	4703
rs749168085	snp	A/G	5.56684e-05	0.00527552	missense	NEB	GRCh38.p7	2:151691913	TATTCTTGTGTTATT[A/G]TCTGAGGGAAATAGC	4703
rs749174010	snp	A/T	0.000108849	0.00737651	intron-variant	NEB, RIF1	GRCh38.p7	2:151494118	CCAAACTGCAAGAGT[A/T]ATTTTGCAAAATTAA	4703
rs749175654	snp	C/T	5.54155e-05	0.00526352	intron-variant	NEB	GRCh38.p7	2:151537095	GGTACAGGTATATGT[C/T]GAATGGATGAGGCCA	4703
rs749185577	snp	C/T	1.79664e-05	0.00299714	missense	NEB	GRCh38.p7	2:151561068	TCTAGAACTGTTGTG[C/T]ATTTGTCCTTAATCT	4703
rs749185640	snp	A/T	1.67225e-05	0.00289154	missense	NEB	GRCh38.p7	2:151678123	ACCAGTTTAGGGTCA[A/T]CTTGAAGACTTTGGA	4703
rs749222946	snp	C/T	1.6902e-05	0.00290701	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151518970	CTGAGCTTACAGAAC[C/T]GGCAAGTTGGCTTGT	4703
rs749224345	snp	C/T	2.41917e-05	0.00347782	intron-variant	NEB	GRCh38.p7	2:151560976	GAAAGGTGGCTCATA[C/T]ATAAGGGGGAAAAAA	4703
rs749224510	snp	C/G	2.30417e-05	0.00339416	intron-variant	NEB	GRCh38.p7	2:151618516	CAGATTTATTAATTA[C/G]TGTTTCAGATTCATA	4703
rs749227055	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151649896	TCTGGGTGTTTCATG[C/T]AGTCAAGTTTCAAAG	4703
rs749228422	snp	A/T	1.67167e-05	0.00289103	missense	NEB	GRCh38.p7	2:151697156	GACTTACGTCTTTAC[A/T]CTGATCTAGTTTCTT	4703
rs749235813	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151618598	AGGTTCCTAGCATAG[C/T]CATTCACTCACTCAC	4703
rs749237360	snp	C/T	1.72119e-05	0.00293354	intron-variant	NEB	GRCh38.p7	2:151640695	AAGACAGATAGTCAT[C/T]TGTTTTAACTTTTAG	4703
rs749251567	snp	C/T	1.66538e-05	0.00288559	intron-variant	NEB	GRCh38.p7	2:151644429	CTTTGAAGTGATAAA[C/T]TGCAATCAAATCAAT	4703
rs749269694	snp	A/G	1.69318e-05	0.00290957	intron-variant	NEB	GRCh38.p7	2:151627476	TGTCTCAGTATTTCT[A/G]TGAATTACTATTATG	4703
rs749270501	snp	A/C/G	3.38805e-05	0.00411571	missense, intron-variant	NEB	GRCh38.p7	2:151609861	ATGTCGTTTTGATCC[A/C/G]GCATGCATGTCCATT	4703
rs749274458	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151493676	GAATTTTTAAAGATA[C/T]ACAAAAGTTTTGGAA	4703
rs749274693	snp	A/T	1.77294e-05	0.00297731	missense, intron-variant	NEB	GRCh38.p7	2:151650593	CTTTGCAGTTCATAA[A/T]CTTTCTTAGCTTGCA	4703
rs749277876	in-del	-/CT/GTTTTT/TTTTTTT			intron-variant	NEB, RIF1	GRCh38.p7	2:151524653	TACTCAAGAGAGAGG[-/CT/GTTTTT/TTTTTTT]CTTTTTTTTTTTTTT	4703
rs749280613	snp	G/T	0.000465178	0.0152438	missense, intron-variant	NEB	GRCh38.p7	2:151631295	CATCCATAGACCCAA[G/T]GGGGACCCAGCCAAT	4703
rs749297993	in-del	-/AC/T			intron-variant	NEB	GRCh38.p7	2:151570470	GCTGAAAAAAAAAAA[-/AC/T]CTGAGAAGTTAAAAA	4703
rs749302235	snp	G/T	1.83849e-05	0.00303185	missense	NEB	GRCh38.p7	2:151545928	TGCACTTTTCTGTAT[G/T]CTGGAGTGTCAAGCA	4703
rs749308804	snp	A/G	1.6577e-05	0.00287893	missense	NEB	GRCh38.p7	2:151662286	GCTTCCAGGGAGCCC[A/G]GAGGGAGCCATCCAA	4703
rs749309632	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151524932	TGGGCTCCCAAAGTG[C/T]TGGGATTATAGGCAT	4703
rs749318184	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151705161	TTATACAAACAATTA[G/T]CCTTCAAAATTATAT	4703
rs749320722	snp	C/G	1.68977e-05	0.00290665	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151493392	CTTAGCTCTCTCCAT[C/G]TCTGGAGTAACAGGT	4703
rs749327025	snp	C/T	1.65641e-05	0.00287781	missense, intron-variant	NEB	GRCh38.p7	2:151614491	CACTCTGGATCTTGG[C/T]CACATGGATGGACCA	4703
rs749332680	snp	C/T	1.65638e-05	0.00287778	synonymous-codon	NEB	GRCh38.p7	2:151680826	ATGTTGGCGATATTT[C/T]TTCTGTTTGGCAAAT	4703
rs749336034	snp	C/T	1.65644e-05	0.00287783	missense	NEB	GRCh38.p7	2:151674544	CCCAGCACATTGTTG[C/T]CCTTGGCTATTAAGT	4703
rs749338317	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151637572	GGAATAGGGGGTTGC[A/G]GGCAAAATGGGGAAG	4703
rs749357193	snp	G/T	0.000580046	0.0170202	intron-variant	NEB	GRCh38.p7	2:151690707	GGGTCACCCACGCTT[G/T]CATAAATCAAAGCAC	4703
rs749362320	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151573416	ATGCCTATGGATTGA[A/G]TGGGAAGAGGCGTCT	4703
rs749368259	snp	C/G/T	5.81074e-05	0.00538984	synonymous-codon, missense	NEB	GRCh38.p7	2:151669129	CTCTACCTTGTAGTT[C/G/T]AACTAAAAACAAAGG	4703
rs749369995	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151671537	TTAAAGCATTTTTTT[C/T]CAAGTCACTTACTGT	4703
rs749374539	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151725196	CCTTACTGTGCTACA[C/G]TGTGGAGAACCACAG	4703
rs749383803	snp	C/T	3.18122e-05	0.00398812	missense	NEB	GRCh38.p7	2:151562751	GCACGTGATTCATCA[C/T]GTCATTGGGGATATG	4703
rs749386509	snp	C/T	1.6569e-05	0.00287824	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151529243	GGCGTCCTTGGCTGC[C/T]TTGATATGAACAGCA	4703
rs749386810	snp	A/G	2.31019e-05	0.00339859	intron-variant	NEB	GRCh38.p7	2:151667958	GACATCATTAAAAGA[A/G]GAATGAAACAGAATG	4703
rs749393120	in-del	-/A	3.37285e-05	0.00410647	intron-variant	NEB	GRCh38.p7	2:151614597	TTGTACTAAAAAAAT[-/A]AGAGATATGAGTATA	4703
rs749393240	in-del	-/ATT	7.62398e-05	0.00617366	intron-variant, utr-variant-3-prime	NEB, RIF1	GRCh38.p7	2:151497765	CATGAGTAACATTTC[-/ATT]ATTTCTTGGGACTTT	4703
rs749395393	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151651410	AAGATACATGACTAA[A/G]TAAATACGCCTAATA	4703
rs749395667	snp	C/T	1.65608e-05	0.00287752	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151524553	GTGTGGCCTTCTTGA[C/T]GTCTGGTCGATCAGC	4703
rs749398319	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151511951	TACAAGTTGTACCAT[A/G]TTCTTCAGTACCTTA	4703
rs749404397	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151544712	TGAGTGTAGGAAGCT[C/G]CATATCCCTCCACTG	4703
rs749408883	snp	G/T	1.6669e-05	0.00288691	intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151534211	GCCAGCCCCATCACA[G/T]TACCTGACTGATCTG	4703
rs749414615	snp	A/G	1.65853e-05	0.00287964	synonymous-codon	NEB	GRCh38.p7	2:151710464	AGCATTCATTCTGGC[A/G]TTTGCAACTTCAAAG	4703
rs749417645	snp	A/G	3.14629e-05	0.00396616	missense, intron-variant	NEB	GRCh38.p7	2:151630723	CTCCTACCTCACTGT[A/G]GTTGATTTTGTTCTG	4703
rs749419926	snp	C/G	1.6566e-05	0.00287797	missense	NEB	GRCh38.p7	2:151725494	TGATTCTGCGAAGTT[C/G]TGGAGTATCTGTTGT	4703
rs749434786	snp	C/T	1.65723e-05	0.00287852	synonymous-codon	NEB	GRCh38.p7	2:151567285	AAGGGTCTGCCCCTG[C/T]TTGGCGGCCAAGACT	4703
rs749444070	snp	C/G	1.69321e-05	0.0029096	intron-variant	NEB, RIF1	GRCh38.p7	2:151492523	GACCGTGAATGAGTG[C/G]TGCTGTCCTAAATCT	4703
rs749446572	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151727613	AAACAAATCCAGCCA[A/G]CATCCAAAACAGAGT	4703
rs749447128	snp	A/T	2.82514e-05	0.00375831	intron-variant	NEB, RIF1	GRCh38.p7	2:151502755	TTATTTTAAATAAAA[A/T]TAAGGGATTTTTTTT	4703
rs749449995	snp	C/T	1.65647e-05	0.00287786	missense, intron-variant	NEB	GRCh38.p7	2:151614388	CTTACAAGGATCTGA[C/T]ACTTCTTGGCCAGCA	4703
rs749452631	snp	C/T	1.65655e-05	0.00287793	missense, intron-variant	NEB	GRCh38.p7	2:151627024	ATATTGAGAGCATTG[C/T]TCTTGGCCAGCACCT	4703
rs749452641	snp	A/G	1.67111e-05	0.00289055	stop-gained	NEB	GRCh38.p7	2:151541470	GAAGCTTCTGCCCTC[A/G]CTTGGCTCTTAAAAG	4703
rs749468828	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151625644	TGTATAAGCGCTGTG[A/T]AGGATAAAAAGGTTA	4703
rs749473348	snp	A/C	1.66012e-05	0.00288103	missense	NEB	GRCh38.p7	2:151696678	GGGCTTGTAGCAGAA[A/C]AGGAGAGTCTGTAAC	4703
rs749473861	snp	C/T	4.96907e-05	0.00498426	missense, intron-variant	NEB	GRCh38.p7	2:151643861	GCATGGATGACATCG[C/T]TCTGGTCGGGCAGGC	4703
rs749477627	snp	A/G	2.25076e-05	0.00335459	intron-variant	NEB	GRCh38.p7	2:151682651	CCCTCTGACACACCC[A/G]GTGGCTTTACCTCAT	4703
rs749496248	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151638693	CTAGGGTGGAGGCTT[C/G]ACTCTCTGCCTAAGC	4703
rs749503444	snp	G/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151487440	CACAAATAGATTTCC[G/T]TTCCCCTTTGCATAA	4703
rs749504940	snp	C/T	1.65908e-05	0.00288012	missense	NEB	GRCh38.p7	2:151576215	TCAACAATGCTTGTG[C/T]ACTTAAGGTTCACCA	4703
rs749508488	snp	A/C	1.65592e-05	0.00287738	missense, intron-variant	NEB	GRCh38.p7	2:151643930	CTGACTAAGGTCTGG[A/C]ACTTCTTGGCCAACA	4703
rs749514411	snp	A/G	1.66632e-05	0.0028864	synonymous-codon	NEB	GRCh38.p7	2:151672425	TCATGGCGTCAGGTA[A/G]GTATGTGTAATGATG	4703
rs749526878	snp	G/T	1.65627e-05	0.00287769	missense, intron-variant	NEB	GRCh38.p7	2:151650723	CCAACATGTCCACTG[G/T]GCTGGAGAACTTAGT	4703
rs749527199	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151561665	TGCAGGTTAGTTACA[C/T]ATGTATACATGCCCC	4703
rs749529584	snp	C/T	1.65737e-05	0.00287864	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151490057	GTTGTGGGAGCTCTG[C/T]GGTTTTTGCATGTTT	4703
rs749535082	snp	C/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151513187	GACAAGCTAAGATGC[C/G]TAAAAACTGTTCTAA	4703
rs749536005	snp	A/G			missense, intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151499389	TTTTCTTTATACAAC[A/G]CCTGTATGACACAAG	4703
rs749542572	snp	A/T	9.3576e-05	0.00683954	intron-variant	NEB	GRCh38.p7	2:151630832	ACGCTATAAAAGAAG[A/T]TAAGATGCTGATTAA	4703
rs749543184	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151545523	GAGGTTGCAGTGAGC[C/T]GAGATTGCGCCATTG	4703
rs749548260	snp	C/T	8.03503e-05	0.00633788	intron-variant	NEB, RIF1	GRCh38.p7	2:151493760	TTAAGGATTTATTTT[C/T]CCTTTCTAAAATACC	4703
rs749549868	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151674066	CCTAAAAAAGTGGAC[G/T]TTTCCCTCTTTGGTT	4703
rs749550758	in-del	-/TT			intron-variant	NEB, RIF1	GRCh38.p7	2:151502763	AATAAAATTAAGGGA[-/TT]TTTTTTTTTTTGGCC	4703
rs749553879	snp	A/G	1.66651e-05	0.00288657	missense	NEB	GRCh38.p7	2:151662169	TTATTCTGGGCCAAA[A/G]CCATGTTCATCGAGT	4703
rs749555452	snp	C/T	3.33673e-05	0.00408442	intron-variant	NEB	GRCh38.p7	2:151710408	CCCTCCCAGGATGAC[C/T]AACCAGCCATCCCTT	4703
rs749556191	snp	C/G	0.000265129	0.0115106	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151609929	AGTCTGACATTTCTT[C/G]GCCAGCAAGATGCTT	4703
rs749556642	snp	C/T			downstream-variant-500B, intron-variant	NEB, RIF1	GRCh38.p7	2:151484979	GCATTACTACGGCTG[C/T]AAAGTTACAGGGACT	4703
rs749556721	snp	C/T	9.9481e-05	0.00705199	intron-variant	NEB	GRCh38.p7	2:151610643	GGAAGGGATAATAGA[C/T]GACAGAAAATAAGAG	4703
rs749557861	snp	G/T	2.55392e-05	0.00357337	missense	NEB	GRCh38.p7	2:151733152	TAGTCTTCGTCATCT[G/T]CCATTTTTCCAGAGT	4703
rs749563453	in-del	-/TTT			intron-variant	NEB	GRCh38.p7	2:151673733	AAATTTTTCTTTTTC[-/TTT]TTTTTTTTTTTTTTT	4703
rs749573099	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151626411	GTGAGACACCATGCC[C/T]GGCTTGCATCTTTCT	4703
rs749577422	snp	A/G	2.22586e-05	0.00333598	intron-variant	NEB	GRCh38.p7	2:151547772	CATTACAGGCATTTA[A/G]TAGGGGACGACGAGG	4703
rs749577487	snp	A/G	1.68038e-05	0.00289855	intron-variant	NEB	GRCh38.p7	2:151540819	GAATAATAGAAGAAA[A/G]TGAGGTGTCATAGAG	4703
rs749580427	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151546704	GCTGGGATTACAGGC[A/G]TACATCATCGTGCCT	4703
rs749583428	snp	C/G	1.66388e-05	0.00288429	splice-acceptor-variant, nc-transcript-variant, intron-variant	NEB, RIF1	GRCh38.p7	2:151506259	CTCTTTATATAAAAC[C/G]TGGGCATTCAGAATC	4703
rs749583969	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151626064	AAATGTACCTGTATG[G/T]GCTATCTCTAGATTT	4703
rs749596914	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151668757	TCCAATCTTGTCTGT[C/T]TCATGTTCCATTTTT	4703
rs749608225	snp	A/G	0.000173705	0.00931786	intron-variant	NEB	GRCh38.p7	2:151655400	GGAAAAAAAGACATG[A/G]AATTTGAATAACTGG	4703
rs749616883	snp	C/G	7.26507e-05	0.00602661	intron-variant	NEB	GRCh38.p7	2:151610896	GGCATGGGGCATGGG[C/G]AGAGGGAGGGAGTAT	4703
rs749620604	in-del	-/A			intron-variant	NEB, RIF1	GRCh38.p7	2:151532358	AATATTGTTTTACTC[-/A]TAACATATTGTATTG	4703
rs749630865	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151711253	TTTTGAAATACCTTG[A/G]CTGAAGTGTTCTTGG	4703
rs749631051	snp	C/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151486752	AAAGGACGCCATGCA[C/G]CAAGGTCAGTATATT	4703
rs749635922	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151661527	GCTGCAGTTATTTTA[C/T]TACTTTTAACTTCAA	4703
rs749638353	in-del	-/CTT	1.65625e-05	0.00287766	cds-indel, intron-variant	NEB, RIF1	GRCh38.p7	2:151505502	GTGCTTCTGCGTCTC[-/CTT]CACACGTTTCACTTC	4703
rs749649342	snp	C/G	1.66103e-05	0.00288182	intron-variant	NEB	GRCh38.p7	2:151692241	CCTCCTACCCGAAAG[C/G]TAACCGTGGCTTTTC	4703
rs749655119	snp	C/T	3.34689e-05	0.00409064	missense	NEB	GRCh38.p7	2:151677902	TCTGCATCATGTTCT[C/T]AGACAGCTCCAGGTC	4703
rs749661136	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151611966	GCATCACTCCAGGGA[A/T]ATCATTCCAGGCTCT	4703
rs749666647	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151563580	TATGGGGCACAAATC[C/T]CGTGTTAAAGTGGAC	4703
rs749668960	snp	A/T	3.3248e-05	0.00407712	intron-variant	NEB	GRCh38.p7	2:151618247	TGTGGTAACTTTCGG[A/T]ATCTAACAGTGAGGA	4703
rs749677571	in-del	AT/GTCAAGTAAAAGGAAA			intron-variant	NEB	GRCh38.p7	2:151578277	CACATTGTGAAGAAC[AT/GTCAAGTAAAAGGAAA]CAAGTGGTCTGGAGT	4703
rs749690481	snp	A/G	3.33078e-05	0.00408078	intron-variant	NEB	GRCh38.p7	2:151546479	TATAGCTGGTCATAA[A/G]CAAATGTAAGTCAGG	4703
rs749691023	snp	A/C	2.46984e-05	0.00351405	intron-variant	NEB	GRCh38.p7	2:151662090	GTAAATTATACCTGG[A/C]TTCTCTCTGATGCAT	4703
rs749691317	snp	G/T	1.65844e-05	0.00287957	missense, intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151534308	CTGCTCATAATCAGC[G/T]CTGTATTTTTTCTGC	4703
rs749692165	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151645100	CACCGTCCTGTATGT[C/G]TGCCTTTGTTGGCCA	4703
rs749694311	in-del	-/GA	1.65493e-05	0.00287652	intron-variant	NEB	GRCh38.p7	2:151677850	ACTTAATAGGGGGGT[-/GA]TTCTTGAGAAGTAAA	4703
rs749700121	snp	C/T	3.01818e-05	0.00388459	intron-variant	NEB	GRCh38.p7	2:151568613	TAAAACAGCCATATA[C/T]TTACATCATCGAGGA	4703
rs749713442	snp	A/C/T	4.96992e-05	0.00498473	missense	NEB	GRCh38.p7	2:151576270	AAAAGATATTCTGGG[A/C/T]GTTTTTGACTCTCAA	4703
rs749714601	snp	C/T	6.62361e-05	0.00575445	missense, intron-variant	NEB	GRCh38.p7	2:151640452	TTGTAGTCCACATCG[C/T]TGACTAAGGTCTGGC	4703
rs749715395	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151566333	CCTTCAAGAACCTAG[A/T]TTCTCCCAGCCAACT	4703
rs749717087	snp	C/T	1.6593e-05	0.00288031	intron-variant	NEB	GRCh38.p7	2:151562107	TCTAGGAAGGTGGCT[C/T]ACCTGACTCTGAAGG	4703
rs749718307	snp	A/G	1.65652e-05	0.0028779	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151627089	CTTGTCCGGAGGCTG[A/G]CGGTAGATGTTATCA	4703
rs749718917	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151487760	AACTTATTTTATACA[C/T]ACACACATATATATA	4703
rs749757964	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151679614	TTTCAATCAGATTTG[C/T]TTCCAATTGGGGACT	4703
rs749780816	snp	C/G	1.65767e-05	0.00287891	missense	NEB	GRCh38.p7	2:151569300	CGGCATGTTTGGCAT[C/G]ATTGACGGACACGGA	4703
rs749789516	snp	C/T	1.88177e-05	0.00306733	synonymous-codon	NEB	GRCh38.p7	2:151724320	GGCATCAGGAGGAAG[C/T]AGGTACTTATCCTTG	4703
rs749804170	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151519888	GTGATCATATAATCT[A/G]TTATCCAAACTGGGA	4703
rs749807202	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151552939	ACAGTGTAACCAACA[C/T]TTATATGGGGCTTCT	4703
rs749827507	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151732637	TATAAAGTCTCACAT[C/T]TGCATATAATTTCAT	4703
rs749832597	snp	A/G	3.53845e-05	0.00420606	missense, intron-variant	NEB	GRCh38.p7	2:151609837	TCATAGGCCTTTTTT[A/G]CTTGGATAATGTCGT	4703
rs749837540	snp	A/G	1.65592e-05	0.00287738	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151633747	GTTCTTATAGTCCAC[A/G]TCACTGACTAAGGTC	4703
rs749842408	in-del	-/AC	0.000103634	0.00719766	intron-variant	NEB	GRCh38.p7	2:151546014	TTAAAAAAAAAAAAA[-/AC]AAAACAGAAATACAA	4703
rs749846221	snp	A/G	1.65608e-05	0.00287752	missense	NEB	GRCh38.p7	2:151672548	TTTTGGTGTTCTCAT[A/G]GTTCTTCTTGTATTC	4703
rs749846777	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151567927	CGAAAAGTGAGCAGG[C/T]ACTCCAACCATCACC	4703
rs749861183	snp	A/G	1.65666e-05	0.00287802	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151524597	TGCAGGTTCTCTTTG[A/G]CATCTTTTCTGTAAG	4703
rs749865900	snp	C/T	1.65616e-05	0.00287759	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151633708	ATCGCTCTGGTCAGG[C/T]AGGCATGTCCACTCG	4703
rs749875634	snp	C/T	1.66054e-05	0.00288139	missense	NEB	GRCh38.p7	2:151567349	TTTGTTTTGTGATAG[C/T]CCTCTTTGTATAGTC	4703
rs749876066	in-del	-/AA			intron-variant	NEB	GRCh38.p7	2:151694636	ATAAAGATTCTGGAC[-/AA]AAAAATTCAGCAAAG	4703
rs749884138	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151672174	TAATAAAGACAGCAT[C/T]AATAATTATGATATA	4703
rs749884255	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151686636	ATGTATAGATCATTA[C/T]ATAAAAGCATGGTTA	4703
rs749892783	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151569848	TATTTTCACAGTTTT[C/T]TTTAATCTGATACAA	4703
rs749894317	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151626228	CAGGTGATCCTCCCA[C/T]CTCAGCCTCCCAAGT	4703
rs749905917	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151670132	GAGAAGTGACATCTC[A/G]CTCAGTACAAAAGAA	4703
rs749913865	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151545147	TAGTCTGAATTGTAC[C/T]GAATGGGCAGCAGAG	4703
rs749915004	in-del	-/A/AA	0.29639	0.268522	intron-variant	NEB	GRCh38.p7	2:151617472	GTATATAAGCGCTAC[-/A/AA]AAAAAAAAAAAAAAA	4703
rs749915831	snp	C/G	2.29471e-05	0.00338718	missense	NEB	GRCh38.p7	2:151562703	AGTGTCGATACTCCA[C/G]GTCACTGAGGATGTA	4703
rs749924365	snp	C/T	1.81335e-05	0.00301105	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151493353	AGTCCTAGAAAATAC[C/T]GAGCTAATGTTTTCT	4703
rs749927128	snp	C/T	0.000104912	0.00724188	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151625600	AGGCATAATATGGAC[C/T]TGGGTCTTGTCTTTG	4703
rs749939967	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151722357	CTGCTGGTTTCAAGC[C/G]TAAGGACTCTGTTAA	4703
rs749945086	snp	A/C	1.85675e-05	0.00304687	intron-variant	NEB	GRCh38.p7	2:151650545	AATATGAATTAATAT[A/C]TAAACTATTGGATTT	4703
rs749953597	snp	A/C			intron-variant	NEB, RIF1	GRCh38.p7	2:151500318	GGATTAATTCCCACT[A/C]CCCAGAAAAAAATCC	4703
rs749953873	snp	A/G	4.97558e-05	0.00498753	intron-variant	NEB	GRCh38.p7	2:151629510	CCACTTCATCCATCC[A/G]TGTAAATATCTAGGG	4703
rs749955078	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151668197	ATAACAGAAGGTTTT[C/T]ATTTATTTGTCATAA	4703
rs749958402	in-del	-/T	8.33229e-05	0.00645403	intron-variant, utr-variant-3-prime	NEB, RIF1	GRCh38.p7	2:151497600	TCATTAAATAAGTAG[-/T]TTTTTTTCTTTTCTT	4703
rs749959056	snp	C/G/T	4.99924e-05	0.00499941	synonymous-codon, missense	NEB	GRCh38.p7	2:151667861	GATGGCATCTGGTCT[C/G/T]AAATCATAGCCCTTG	4703
rs749972227	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151673013	CTTGGTTTCATAGGG[C/T]TTCATAGGTTTCGAT	4703
rs749977606	snp	A/G	1.66713e-05	0.0028871	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151492448	GTATCCAATACATAG[A/G]CAGCTTTGCCTTGTA	4703
rs749981587	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151710797	GACTTCATTCATTCG[A/G]AAGTTGCAGATGTCC	4703
rs749986606	snp	C/T	1.68182e-05	0.00289979	synonymous-codon	NEB	GRCh38.p7	2:151547649	CTCACTGACAGCCTC[C/T]TGTGTCTTCTTGACT	4703
rs749988845	snp	A/G	8.37009e-05	0.00646865	intron-variant	NEB	GRCh38.p7	2:151725418	TAGGTGTATTTTGAA[A/G]TGTCCCTCTCCTTTA	4703
rs749993364	snp	A/T	3.27434e-05	0.00404606	intron-variant	NEB, RIF1	GRCh38.p7	2:151501351	TTTTGTAGAAATTAT[A/T]ATTTTTTAATATGGA	4703
rs750007272	snp	A/C/G	3.65492e-05	0.00427475	intron-variant	NEB	GRCh38.p7	2:151609760	TGACTGGGCAATGAA[A/C/G]AAATCTACATCTTCC	4703
rs750007608	snp	C/T	1.6563e-05	0.00287771	intron-variant	NEB, RIF1	GRCh38.p7	2:151524508	GACATTTTCATGACA[C/T]CCTTACCTCACTGGC	4703
rs750010017	snp	G/T	1.67559e-05	0.00289442	intron-variant	NEB	GRCh38.p7	2:151640344	ACGTTATTATGACTC[G/T]CAGTACTCACATCGC	4703
rs750018272	snp	A/G	3.37194e-05	0.00410592	intron-variant	NEB, RIF1	GRCh38.p7	2:151490117	TATAAGAAGAAAAAT[A/G]GCTAGGTATCCTTTA	4703
rs750022788	snp	C/T	2.28752e-05	0.00338187	intron-variant	NEB, RIF1	GRCh38.p7	2:151516417	GCTTGTGTTCAGTAG[C/T]GTGATGGATCATTGT	4703
rs750023832	snp	G/T	1.66707e-05	0.00288705	missense	NEB	GRCh38.p7	2:151696645	AACTTACGTCACTCA[G/T]TTGTTTGGAATTGAC	4703
rs750026140	snp	A/G	1.65594e-05	0.0028774	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151643896	CCACTGGTGCAGGTA[A/G]TTCTTGTAGTCCACG	4703
rs750031501	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151611516	TCATATTTGTACTGA[A/G]CACTCAATTGTACTA	4703
rs750039342	snp	C/T	9.16548e-05	0.00676897	intron-variant, missense	NEB, RIF1	GRCh38.p7	2:151533522	CATGTTGCAGAAACA[C/T]CTTGGCACTAGATTT	4703
rs750041475	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151487224	GAATTTGGGAGCATA[C/T]GAGTAGTAAAAGTTT	4703
rs750050167	snp	C/T	1.65734e-05	0.00287862	intron-variant	NEB	GRCh38.p7	2:151626990	TTATTTTCCTACAAA[C/T]TGGGGGCTCACCTTG	4703
rs750051812	in-del	-/T	0.000106992	0.00731331	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151499279	AAATAATTAAAGGGA[-/T]TTTTTTATTTTTAAA	4703
rs750062819	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151660904	CGATTGAGTACTTGA[A/C]ATGTAGCTAATGTGA	4703
rs750062926	snp	C/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151508135	ATTCCAAGAAATAAG[C/G]AGGGTAAACACCACA	4703
rs750063002	snp	C/T	1.68898e-05	0.00290596	synonymous-codon	NEB	GRCh38.p7	2:151576175	ATTTTCAGCATTTGA[C/T]TTAGCAAGGACCACT	4703
rs750064909	snp	A/C	1.6577e-05	0.00287893	synonymous-codon	NEB	GRCh38.p7	2:151729621	GGGCCTTACCTCTCC[A/C]GGCACCTCTTCGTAA	4703
rs750067420	snp	A/G/T	3.32029e-05	0.00407438	missense, intron-variant	NEB	GRCh38.p7	2:151643837	CTCTGGAGGTCATAG[A/G/T]CCTGCCGAGCATGGA	4703
rs750067873	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151692962	ATGACAGAGCGAGAG[A/C]CTGTCTCAAAAAACA	4703
rs750070644	snp	C/T	1.66098e-05	0.00288177	missense	NEB	GRCh38.p7	2:151659168	GCTTGTTTGTAGAGA[C/T]GCTAGGAAAAAAACA	4703
rs750085420	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151501915	CTAGCTTTCAATGAT[A/G]CTGAAAGTTTTCCAA	4703
rs750100838	snp	C/G	1.72074e-05	0.00293316	intron-variant	NEB	GRCh38.p7	2:151541437	CAGGCTTATGAACCT[C/G]TGAGCTTACCTGACT	4703
rs750103810	snp	C/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151532871	AAAGTGCATGCTTCA[C/G]TTGGCCTTCTAAAAA	4703
rs750109772	snp	A/T	6.20771e-05	0.00557088	missense	NEB	GRCh38.p7	2:151709723	GTCTGCATGAAGTAG[A/T]TCTGGTCTTTCATGT	4703
rs750111822	snp	A/G	1.65941e-05	0.00288041	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151609890	TTCATGCAGGTAATT[A/G]CGATAATCAATGTCA	4703
rs750113592	snp	C/T	3.32751e-05	0.00407878	missense, intron-variant	NEB	GRCh38.p7	2:151650663	GGTAGTTCTTGTAGT[C/T]CACGTCACTAACCAA	4703
rs750121360	snp	C/T	1.65619e-05	0.00287762	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151505509	TGCGTCTCCTTCACA[C/T]GTTTCACTTCAGGCA	4703
rs750122752	in-del	-/C	2.27464e-05	0.00337234	intron-variant	NEB	GRCh38.p7	2:151662112	CTGATGCATATGAAA[-/C]ACTGCATTATTGAAA	4703
rs750124596	snp	C/T	1.65864e-05	0.00287974	missense, intron-variant	NEB	GRCh38.p7	2:151618283	GACTCACCTTATTCA[C/T]GTTTAAAGCATTGTT	4703
rs750129587	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151612625	CTTTAATGCTATTCA[C/T]TTTCAGTGATAAAAA	4703
rs750137329	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151671417	TGTTAGAGTGCATTA[C/T]ACAACACAGAAGGGA	4703
rs750141196	snp	C/G	5.22507e-05	0.00511103	missense	NEB	GRCh38.p7	2:151562793	TGGTATCCTCATAAT[C/G]TTTTCTGTAGTTCAA	4703
rs750145113	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151662111	TCTGATGCATATGAA[A/G]CACTGCATTATTGAA	4703
rs750150665	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151645966	CATAGTGAGTACTAA[C/T]ATTTCGATATTCAAT	4703
rs750152377	snp	A/C/T	8.29269e-05	0.00643874	missense	NEB	GRCh38.p7	2:151540756	TGGTCTGGTTTCCAG[A/C/T]GTGATGATGGGGTCT	4703
rs750172942	snp	C/G	3.34096e-05	0.00408702	missense, intron-variant	NEB	GRCh38.p7	2:151610854	CAGCATCCCAAGCTT[C/G]TGTGTATAAATGCTA	4703
rs750175349	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151488631	AGCCTGGGTGATAGA[A/G]TGAGACCCTGTCTCT	4703
rs750186349	snp	C/T	3.31384e-05	0.00407039	missense	NEB	GRCh38.p7	2:151692166	AGTCTTTATATCTAG[C/T]CTGAAAAATAAAACA	4703
rs750186471	snp	A/C	3.31219e-05	0.00406938	missense, intron-variant	NEB	GRCh38.p7	2:151633717	GTCAGGCAGGCATGT[A/C]CACTCGTGCAGGTAG	4703
rs750187840	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151647537	CTGGCACCATCACTT[C/T]AACCAAGTGTTTAAG	4703
rs750188445	snp	A/C/G	0.000132059	0.00812495	intron-variant	NEB	GRCh38.p7	2:151684994	TGAATAGGAAATTAT[A/C/G]ATTTATTATCACAAA	4703
rs750205781	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151552529	CAATAGCCAGCAGCA[C/T]CTTCAGTGCTTTCAA	4703
rs750207141	snp	A/G	1.80977e-05	0.00300808	missense	NEB	GRCh38.p7	2:151655356	TCTTATCTTTATTCC[A/G]ATCAATGGTGTATAA	4703
rs750212562	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151680991	GAATGCAATACAAAA[G/T]TCAATATCTTTAAAA	4703
rs750215416	snp	C/T			missense	NEB	GRCh38.p7	2:151567290	TCTGCCCCTGCTTGG[C/T]GGCCAAGACTGACAC	4703
rs750219813	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151683857	ATAAAATATGGCATA[C/T]CGATACAATAGAATA	4703
rs750221285	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151633540	TATTCTGATTTAAAT[A/C]TTATTCATGGACCAA	4703
rs750225285	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151645464	AAGCTTAAGTGAAAG[A/T]ATTTGTTTTTTCAGA	4703
rs750233465	snp	A/G	1.65847e-05	0.0028796	intron-variant	NEB, RIF1	GRCh38.p7	2:151526124	GGGCGTTCTCCCAAG[A/G]GGGAAGCAGAACTCA	4703
rs750242909	snp	A/C	1.71849e-05	0.00293124	intron-variant	NEB	GRCh38.p7	2:151696750	GCTGTGGGGAAGCAA[A/C]GGCATTTGGTTTAGT	4703
rs750247193	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151553821	ACTTCTTAAGTCACA[A/G]GCTTACATCGCTGAT	4703
rs750260952	in-del	-/TTC	1.65611e-05	0.00287755	cds-indel	NEB	GRCh38.p7	2:151672550	TTGGTGTTCTCATAG[-/TTC]TTCTTGTATTCACGA	4703
rs750262941	snp	C/T	3.54975e-05	0.00421278	intron-variant	NEB	GRCh38.p7	2:151551714	CGGATTTCTGCTGGG[C/T]ACTCTCAAGTTCTCA	4703
rs750264857	snp	A/T	4.10341e-05	0.00452939	intron-variant	NEB	GRCh38.p7	2:151672336	CATCCTTTAAGTGCA[A/T]ACATCTCTGGGTCTG	4703
rs750274374	snp	C/G/T	3.31188e-05	0.00406921	synonymous-codon, missense, intron-variant	NEB	GRCh38.p7	2:151640421	GGGCAGGCATGTCCA[C/G/T]TGGTGCAGGTAGTTC	4703
rs750276279	snp	A/C/G	0.000149072	0.00863235	missense	NEB	GRCh38.p7	2:151692103	AGTGTGTGTGATATG[A/C/G]GTCCTCCATGCTGCC	4703
rs750278744	snp	A/C	5.01065e-05	0.00500507	intron-variant	NEB	GRCh38.p7	2:151677826	GGGTTCTTTTCATGG[A/C]AGGCTCTGAACTTAA	4703
rs750285243	snp	C/G	1.68655e-05	0.00290387	intron-variant	NEB	GRCh38.p7	2:151568434	TAAAAAAAAAAAAAT[C/G]AGAGGCAAGGGGGCA	4703
rs750290748	in-del	-/C			intron-variant	NEB	GRCh38.p7	2:151658175	CTACCACTGTGGCGT[-/C]CTTTTTTTTTGTTTT	4703
rs750302574	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151668887	CGCCCCCTAGGCTCA[C/T]GTTGCATGGTTAAGG	4703
rs750304427	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151505319	TGGTTTCTTATCTAC[C/T]TTTGCAACCTGTAGT	4703
rs750311680	snp	C/G/T	1.65866e-05	0.00287976	intron-variant	NEB, RIF1	GRCh38.p7	2:151505612	AGGTATTATTACATG[C/G/T]TGGACTGTTATTCTT	4703
rs750316684	snp	A/C	1.65902e-05	0.00288008	synonymous-codon	NEB	GRCh38.p7	2:151546414	GCAGCCAAATCCCTT[A/C]AGGACCTGCAAGTCC	4703
rs750321888	snp	C/T	1.65982e-05	0.00288077	intron-variant	NEB	GRCh38.p7	2:151697541	GACAGTAGGATTGCT[C/T]ACATCACTACTGAAG	4703
rs750337661	snp	G/T	1.65798e-05	0.00287917	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151519684	GATTATTAGCATCTT[G/T]CATGACTTTGTAGAG	4703
rs750345178	snp	C/T	1.66092e-05	0.00288172	intron-variant	NEB	GRCh38.p7	2:151655783	TAGCCTTTCCTCACG[C/T]GGGAGCTGTGTGGAC	4703
rs750352913	snp	A/C	1.65608e-05	0.00287752	missense	NEB	GRCh38.p7	2:151666272	TGCTGGCTTCATAGC[A/C]CTTTTTGTACTCACG	4703
rs750353626	snp	C/G	4.29729e-05	0.00463515	intron-variant	NEB	GRCh38.p7	2:151723509	AAAAAAGAGTGAAAA[C/G]TTAGGAGGAAGTAGG	4703
rs750355299	snp	C/T	1.66034e-05	0.00288122	missense, intron-variant	NEB	GRCh38.p7	2:151612203	TGCTCATTGTCAGGG[C/T]ATTATTCTTTGCTAG	4703
rs750360947	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151559962	AACAAAACACACACA[C/G]GCAAAAAGGTTTTAC	4703
rs750363714	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151557524	CTCATTTTATGAGGC[C/T]GGCATCATCCTGATA	4703
rs750374820	snp	A/G	0.000117293	0.00765721	synonymous-codon	NEB	GRCh38.p7	2:151537946	ACCTCCAGATACCCA[A/G]CTGGCTCATGTAGTT	4703
rs750375108	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151494810	TGCACCACCATGCCC[A/G]GCTAATTTTTGTATT	4703
rs750375788	snp	G/T	1.66793e-05	0.0028878	missense	NEB	GRCh38.p7	2:151551797	CGGTTTTGGTAGTTG[G/T]AGCCACTTTGCCTCT	4703
rs750385058	snp	C/T	7.04871e-05	0.00593621	missense, intron-variant	NEB	GRCh38.p7	2:151646213	GAGTCTTGTCTTTGT[C/T]CCAAGCTTCTCTATA	4703
rs750390546	snp	A/C	0.000308499	0.0124159	missense, intron-variant	NEB	GRCh38.p7	2:151591420	CAGGTCATAACCAGT[A/C]ATCTTGACATCTTCC	4703
rs750392223	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151658758	AAATTCTAGGACTCT[A/C]ATTTCCTTTTTCTCT	4703
rs750393216	snp	A/G	6.67327e-05	0.00577597	missense	NEB	GRCh38.p7	2:151565545	CTAAAACAATCTCTG[A/G]AGGATCCACCACACT	4703
rs750399192	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151621156	TAAATCAGAAAAAGA[A/T]CTCTTTCTTTTACTT	4703
rs750403649	snp	G/T	7.48923e-05	0.00611887	intron-variant	NEB	GRCh38.p7	2:151646091	TAGAAACAATTAAAA[G/T]GAGCTTTCTGAAAAC	4703
rs750404540	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151591035	CACCGGTAGTATACA[C/T]GCCACACTTTGAGTA	4703
rs750405935	snp	A/C			intron-variant	NEB, RIF1	GRCh38.p7	2:151493490	CAGACAGCAGAAAAC[A/C]AGGTCTGAAAATCAT	4703
rs750414431	snp	C/T	1.68306e-05	0.00290087	intron-variant	NEB	GRCh38.p7	2:151546342	GTGATGATGTGCACT[C/T]ACCCAGAGCTTCCGC	4703
rs750421861	snp	A/C	1.671e-05	0.00289045	missense, intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151496947	CCCAAGTACCGAGCT[A/C]ATATTTTCTTGATTG	4703
rs750437206	in-del	-/A	0.00015266	0.00873537	intron-variant	NEB, RIF1	GRCh38.p7	2:151493767	TTATTTTTCCTTTCT[-/A]AAAATACCGAGCTAA	4703
rs750445824	snp	C/T	1.66178e-05	0.00288247	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151503430	TGTTCCCAAGTTTTC[C/T]TTGTACATAACCTGT	4703
rs750455026	snp	C/T			intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151499047	ATAAATGTGGATGCT[C/T]AGACACTGAGAATGT	4703
rs750468623	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151541634	TTCACTGCTTTTACA[C/T]AGAAAAGGCAGGAGC	4703
rs750480211	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151708721	GTGGATGTCTAAAAG[C/G]CATCTCAAATCTACC	4703
rs750480680	snp	A/C	6.62508e-05	0.00575508	missense	NEB	GRCh38.p7	2:151658006	CAATATCTCTGGAAG[A/C]CTTGGCAGCTTTGAT	4703
rs750481145	snp	C/T	1.65608e-05	0.00287752	intron-variant	NEB, RIF1	GRCh38.p7	2:151525932	TGGCATTGTTGCTGC[C/T]AAGAGACCGGTGGTT	4703
rs750498117	snp	C/G	1.65795e-05	0.00287914	missense	NEB	GRCh38.p7	2:151548323	CTCGCTGGTAACATT[C/G]TTGACTCTCCGGACG	4703
rs750502323	in-del	-/T	8.90697e-05	0.00667285	frameshift-variant, intron-variant	NEB	GRCh38.p7	2:151630729	CCTCACTGTAGTTGA[-/T]TTTGTTCTGCCTTGC	4703
rs750523537	snp	A/T	2.74729e-05	0.00370617	missense, intron-variant	NEB	GRCh38.p7	2:151621020	CCATGGCCTGACGAT[A/T]GAGGCTCTGAGGAAA	4703
rs750532795	snp	A/G	5.12913e-05	0.00506389	intron-variant	NEB	GRCh38.p7	2:151614615	AGATATGAGTATAAT[A/G]ACAAGAACATCTTAT	4703
rs750535430	snp	A/G	4.67716e-05	0.00483566	missense	NEB	GRCh38.p7	2:151675358	TCATGGTGTATTTAT[A/G]TTTCACATCTTCTCC	4703
rs750541601	snp	A/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151514210	CTGAAAATGAAAAGC[A/T]CTGTTTTTCTCTGTT	4703
rs750548574	snp	A/T	3.32901e-05	0.0040797	missense, intron-variant	NEB	GRCh38.p7	2:151640659	CGATAGCCTTCTTTG[A/T]ACTTGAACTAAAAGA	4703
rs750555338	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151577203	TCCCATCGGTCATAG[A/G]ATAAACATCAAAATC	4703
rs750556090	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151688501	TTAGAAAAATGCCTC[A/G]AAGAGATACTCAATT	4703
rs750572050	snp	C/G	3.31329e-05	0.00407005	intron-variant	NEB, RIF1	GRCh38.p7	2:151514312	GGCAGTCAGCTGTGG[C/G]CCTACCTCATTGAGG	4703
rs750572273	snp	C/T	1.6681e-05	0.00288794	intron-variant	NEB, RIF1	GRCh38.p7	2:151503338	TTCTTATATGATATA[C/T]TTGTAAATACCGAGC	4703
rs750581337	snp	A/G	1.67486e-05	0.00289379	missense, intron-variant	NEB	GRCh38.p7	2:151639900	GCCAACACTTGTTCC[A/G]GAGAGTCAGTCACAC	4703
rs750582285	snp	C/T	1.68088e-05	0.00289899	missense	NEB	GRCh38.p7	2:151717424	TACTTACCTTGCTCA[C/T]TTGATTGGTTACTTT	4703
rs750585238	snp	A/C	3.39795e-05	0.00412172	splice-donor-variant	NEB	GRCh38.p7	2:151695577	GGCATAAGGAACTTA[A/C]ATCACTCAAGTTATA	4703
rs750590997	in-del	-/CAAA			intron-variant	NEB	GRCh38.p7	2:151626509	AACTCTTATAGACTT[-/CAAA]CAATTTGAACCCATA	4703
rs750592605	snp	A/G	1.91653e-05	0.00309553	missense	NEB	GRCh38.p7	2:151563881	ATGTAGCGCTCATCC[A/G]GGGTGTAGCCATAGG	4703
rs750607570	snp	G/T	5.17639e-05	0.00508717	intron-variant	NEB	GRCh38.p7	2:151560957	CTTACTGTCCCAGAA[G/T]GGGGAAAGGTGGCTC	4703
rs750607813	in-del	-/TAGAG			intron-variant	NEB	GRCh38.p7	2:151731356	TTTTCAAGTTTAAGT[-/TAGAG]TAGAGAGAACAGTAA	4703
rs750620305	snp	A/C	1.77055e-05	0.00297531	intron-variant	NEB	GRCh38.p7	2:151691984	CTATAATGAGAAAAA[A/C]CAAAAATAGATCATG	4703
rs750627350	snp	C/T	0.000111414	0.00746289	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151514863	ATGTAACAAAGCTGG[C/T]GTGACCTCCAGGCCA	4703
rs750629199	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151675190	GGGATTTGTGAGAAA[C/T]GGGCCTAAATAAATT	4703
rs750640967	snp	C/T	1.66721e-05	0.00288717	intron-variant	NEB	GRCh38.p7	2:151644144	ACTAGAGAAAAAAAA[C/T]GTGTCTCATTCCTTT	4703
rs750641025	snp	A/G	2.14167e-05	0.00327229	intron-variant	NEB	GRCh38.p7	2:151654125	AAGATATTCTTCAGC[A/G]TTATTCTGTCTATAT	4703
rs750642580	snp	A/T	1.65611e-05	0.00287755	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151526005	GAACAGTGTCCCGGG[A/T]CTCTGGTAGTGTTGT	4703
rs750642880	snp	G/T	1.65619e-05	0.00287762	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151518367	AGCTGCTCCAGATTA[G/T]CGGGTATGGTGTGGT	4703
rs750645150	snp	A/G	1.66114e-05	0.00288192	intron-variant	NEB	GRCh38.p7	2:151568301	AAACACCAGGCATGT[A/G]GGTGAAACCCATACC	4703
rs750647701	snp	C/G	4.70566e-05	0.00485037	missense	NEB	GRCh38.p7	2:151545890	AAAGCGTCCTTACCT[C/G]ACTCAGATGTGTCTT	4703
rs750650533	in-del	-/G			intron-variant	NEB	GRCh38.p7	2:151581688	CTTGAATAAATGGAT[-/G]ATGAAAAAAATTTTA	4703
rs750657732	snp	G/T	1.67936e-05	0.00289767	missense, intron-variant	NEB	GRCh38.p7	2:151654016	AATGTCTCTTGAAGC[G/T]TTAGCTAGCTGTACA	4703
rs750659953	snp	C/T	3.34431e-05	0.00408906	intron-variant	NEB	GRCh38.p7	2:151563796	GTAAAGACTCTCAAA[C/T]TTAGGAGAGGAAAAG	4703
rs750664746	in-del	-/TCTATA	1.65611e-05	0.00287755	intron-variant	NEB, RIF1	GRCh38.p7	2:151514428	CTTTCCTGTACTCTT[-/TCTATA]TCATGAAAGAAAAGC	4703
rs750676739	snp	C/T	1.65861e-05	0.00287972	missense	NEB	GRCh38.p7	2:151671156	GCTTTCTTGACCTTC[C/T]CCACCTCCAGGGAAC	4703
rs750679086	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151678437	GAGATGGGGCATTAC[C/G]ATAATTTGTATCAGT	4703
rs750685144	snp	A/C			intron-variant	NEB, RIF1	GRCh38.p7	2:151503714	TAAATAAATTTACCA[A/C]TGAGAAAAATCTAAC	4703
rs750689059	snp	C/G	2.43058e-05	0.00348601	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151508040	TCTCCCGGACTCTCT[C/G]TATCTCTGGGGTGTC	4703
rs750690457	in-del	-/GT			intron-variant	NEB	GRCh38.p7	2:151675774	AGAGAGAAAGTAGTA[-/GT]TAGAATAAGTTTTTC	4703
rs750690826	snp	C/G	2.90896e-05	0.00381366	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151494188	TTCTTGATTGCGTTT[C/G]ACTCTCTGCATCTCA	4703
rs750698659	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151548773	ACTGACAAATAGCTT[C/T]GTGGACTGATTTTAA	4703
rs750704829	snp	G/T	1.66335e-05	0.00288383	missense	NEB	GRCh38.p7	2:151548413	GGCTTCTTTGTACTT[G/T]AACTGCAAAAGCAAA	4703
rs750705899	snp	C/T	4.97913e-05	0.00498931	missense, intron-variant	NEB	GRCh38.p7	2:151610524	TACTCACGTCACTGG[C/T]GATGTCCCTGGAGGC	4703
rs750709191	in-del	-/AGAT	1.69882e-05	0.00291441	intron-variant	NEB	GRCh38.p7	2:151640685	AAAGAAGAAAAAGAC[-/AGAT]AGTCATCTGTTTTAA	4703
rs750709906	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151548101	TTTGCATCATAATCT[A/G]TGGAACCGAGTCTCT	4703
rs750721746	snp	C/T	1.75256e-05	0.00296015	missense	NEB	GRCh38.p7	2:151561029	AGATTCTTCAGGTTT[C/T]TGGTTCTGTCATAAT	4703
rs750732324	in-del	-/T			intron-variant	NEB	GRCh38.p7	2:151689878	ATACTGATGCCATTC[-/T]TCCTCTTTACTAATT	4703
rs750732565	snp	C/T	3.35008e-05	0.00409259	missense	NEB	GRCh38.p7	2:151665410	TGAACTTCAGCTTCT[C/T]GGGGTGCTGGCGATA	4703
rs750737380	snp	C/G	3.00802e-05	0.00387804	intron-variant	NEB, RIF1	GRCh38.p7	2:151527443	TATTTCTCAGGTGCA[C/G]TATGCAGTTACAATC	4703
rs750748717	snp	A/C			missense, intron-variant	NEB	GRCh38.p7	2:151614296	TCTGCAGGTCATAGG[A/C]CTTCCGAGCCTGAAT	4703
rs750760976	snp	A/C	3.45471e-05	0.004156	intron-variant	NEB	GRCh38.p7	2:151546014	CTTAAAAAAAAAAAA[A/C]AAAACAGAAATACAA	4703
rs750762588	snp	C/T	1.6623e-05	0.00288292	missense	NEB	GRCh38.p7	2:151678072	TCTTTTTTATACTCC[C/T]GATCTGATTGTATCT	4703
rs750769675	snp	C/T			missense	NEB	GRCh38.p7	2:151662329	AGTCAGCATAGTCAG[C/T]CTTGTACTGATTCTG	4703
rs750771590	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151713760	CTGACTGTTCATCTA[C/T]GTTAGAGCTACAAAA	4703
rs750778420	snp	A/G	2.75486e-05	0.00371127	intron-variant	NEB	GRCh38.p7	2:151692498	AATTTTCCACAAAGC[A/G]GAAAAGCAGAATAGA	4703
rs750779863	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151625827	AAATGTATACTAAGA[C/T]ATGAAAAGAAAAATA	4703
rs750788670	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151732411	TGTAAAATGTGTTAG[A/T]TGTCCACTAATAATT	4703
rs750788902	snp	A/T	2.64988e-05	0.00363988	intron-variant	NEB	GRCh38.p7	2:151678223	CATAATTTAAAATGT[A/T]GTTTTGAGGGCTTTA	4703
rs750794609	snp	A/G	1.68264e-05	0.0029005	intron-variant	NEB	GRCh38.p7	2:151535814	GAAAAAACAGAACAT[A/G]GTTACTTGACAGCAG	4703
rs750798983	in-del	-/G	3.31879e-05	0.00407343	intron-variant	NEB, RIF1	GRCh38.p7	2:151524304	CCAGTGCACCCATCT[-/G]CATTACCTGGCTGCT	4703
rs750799792	snp	C/T	1.65828e-05	0.00287943	missense, intron-variant	NEB	GRCh38.p7	2:151640647	CCGAGCTGCTTACGA[C/T]AGCCTTCTTTGTACT	4703
rs750807425	snp	G/T	1.78957e-05	0.00299124	missense	NEB	GRCh38.p7	2:151684866	AAGATGTGCTTATAA[G/T]CAACGTCGCTGGCAA	4703
rs750810441	snp	C/T	0.00785504	0.0621757	missense, intron-variant	NEB	GRCh38.p7	2:151581575	CTTTCTCCCAGGCAT[C/T]GCGATACAATGGCTG	4703
rs750810861	snp	A/G			synonymous-codon	NEB	GRCh38.p7	2:151663818	GCTCCGGAAGCCAAT[A/G]TGTTTCCCTTTGGCT	4703
rs750824184	snp	A/G	3.31318e-05	0.00406999	missense, intron-variant	NEB	GRCh38.p7	2:151627549	GGTCATAGGCCTGCC[A/G]AGCATGGATGACATC	4703
rs750828421	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151730161	TATATCCACATCTCA[A/G]TTATTCCTATACCCT	4703
rs750835495	snp	C/G	1.65715e-05	0.00287845	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151644483	TTCACTGGCAATTTC[C/G]CGGGAGGCTTTTGCT	4703
rs750836832	in-del	-/CAGCCATCCA	3.63392e-05	0.00426243	intron-variant	NEB	GRCh38.p7	2:151724832	TGCTACTGAGTACCC[-/CAGCCATCCA]CAGCCATCCATATCA	4703
rs750849844	snp	G/T	6.62603e-05	0.0057555	intron-variant	NEB	GRCh38.p7	2:151697336	GAAAGTCAAACAATT[G/T]TCTTAGAACTTACAT	4703
rs750859605	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151695936	CCCTGCGTAGCACAA[C/T]TGTCCCTGCAGGTTC	4703
rs750862012	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151569605	TCCATTCTGGTTATT[G/T]TTACTAAGGGATAAT	4703
rs750863262	snp	C/T	0.00692033	0.0584147	missense, intron-variant	NEB	GRCh38.p7	2:151579577	CTGCCCAAACCAGTT[C/T]AGGGTCTTCCTTGGC	4703
rs750863417	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151714980	TATTTTGGATGCACA[A/G]TAGTCATTAAGAACT	4703
rs750872866	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151694472	CCAGATTCCACTCAA[C/G]AGGAAATGTCCCCGA	4703
rs750875873	snp	A/C	1.67374e-05	0.00289282	intron-variant	NEB, RIF1	GRCh38.p7	2:151518469	ATGGAGAAGCTGCTC[A/C]GCATTCCTATTTTTC	4703
rs750892868	in-del	-/T			intron-variant	NEB	GRCh38.p7	2:151676997	CTTTCCTTTAGAAAC[-/T]TTGACTTTAGCCAGA	4703
rs750900690	snp	A/G	1.81936e-05	0.00301603	stop-gained, intron-variant	NEB, RIF1	GRCh38.p7	2:151527528	GGAGGAAGTCCGGTC[A/G]GTCAGGAGTCCACTT	4703
rs750901271	snp	A/G	7.23301e-05	0.0060133	intron-variant	NEB	GRCh38.p7	2:151687767	GCAAAGGAATGATAA[A/G]AACAACAGTGTAATC	4703
rs750904252	snp	G/T	2.35496e-05	0.00343136	intron-variant	NEB	GRCh38.p7	2:151547565	ACCCCAAAACATATG[G/T]ATTAGAGACCGAATG	4703
rs750905463	snp	A/G	3.32231e-05	0.00407559	stop-gained	NEB	GRCh38.p7	2:151567236	GATGACACATCCATT[A/G]GTGCAAGTAATTACG	4703
rs750906423	snp	C/T	1.66771e-05	0.00288761	missense	NEB	GRCh38.p7	2:151724940	TAGTCTTAGCAACAT[C/T]ACCATCCATTCGATA	4703
rs750911075	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151489316	GGTGAACTGTGAAGA[C/T]GATTTGGCTTACCAT	4703
rs750943922	in-del	-/AT			intron-variant	NEB, RIF1	GRCh38.p7	2:151487767	TTTATACATACACAC[-/AT]ATATATATATGTATA	4703
rs750950248	snp	G/T	1.97066e-05	0.00313893	synonymous-codon	NEB	GRCh38.p7	2:151570132	CACATCGTTCTGGTC[G/T]GGCATGCAGGTCCAC	4703
rs750952879	snp	A/G	3.33183e-05	0.00408143	synonymous-codon	NEB	GRCh38.p7	2:151656231	GTACTTGTGAATCAG[A/G]TGCTTGTAGTTAGTG	4703
rs750959127	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151696787	ACCTGTCAGATCCAA[G/T]GTGGCCCACAGGCCA	4703
rs750970430	snp	C/T	1.73033e-05	0.00294132	intron-variant	NEB	GRCh38.p7	2:151672712	GGGTTAGCAAAGTCC[C/T]AGGCATTGATAGCAT	4703
rs750970894	snp	C/T	3.6525e-05	0.00427331	intron-variant	NEB	GRCh38.p7	2:151642559	TAAGGCAAATAACTT[C/T]CCAAGTATACTTACT	4703
rs750971265	snp	C/T	1.78982e-05	0.00299145	intron-variant	NEB	GRCh38.p7	2:151656149	AAGTAGAAGAAAGCC[C/T]TACATCACTCTGTAT	4703
rs750971367	snp	A/T	1.73285e-05	0.00294346	missense	NEB	GRCh38.p7	2:151663548	GTGGTTTTCACGTAC[A/T]TCACTTTGAATCTGC	4703
rs750990726	snp	A/G	0.000115931	0.00761264	missense, intron-variant	NEB	GRCh38.p7	2:151627783	CATCTTCAATGTTCC[A/G]GGCTCCAATGTGGTG	4703
rs751002022	snp	C/T	1.65633e-05	0.00287774	missense	NEB	GRCh38.p7	2:151563634	TTTTGGAAATCCAGA[C/T]AGTGAACCACACCAG	4703
rs751018137	snp	G/T	1.65488e-05	0.00287647	intron-variant	NEB	GRCh38.p7	2:151677852	CTTAATAGGGGGGTT[G/T]CTTGAGAAGTAAATG	4703
rs751019290	snp	A/G	1.65974e-05	0.0028807	intron-variant	NEB, RIF1	GRCh38.p7	2:151505619	ATTACATGCTGGACT[A/G]TTATTCTTCCCAACA	4703
rs751024964	snp	A/G	0.000129391	0.00804232	intron-variant	NEB	GRCh38.p7	2:151664886	GAGAAAGTCAGGTGC[A/G]TGATTTTACAGCAGG	4703
rs751025060	snp	G/T	1.67024e-05	0.0028898	intron-variant	NEB	GRCh38.p7	2:151659185	CTAGGAAAAAAACAG[G/T]GTAAATTAGTGTTTA	4703
rs751032903	snp	C/T	2.56802e-05	0.00358322	intron-variant	NEB	GRCh38.p7	2:151682632	ACAACACAGTCACCA[C/T]TCTCCCTCTGACACA	4703
rs751041067	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151646628	GAAATCAGGAAGTTT[C/T]ATTTCCTATGTGGCT	4703
rs751045077	snp	C/T	1.66021e-05	0.0028811	missense	NEB	GRCh38.p7	2:151555040	TATTCTTCCCGATAT[C/T]TGATCTATAGAGAAT	4703
rs751052601	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151733821	ACAAAGTTGTAAAGC[A/T]TTGATTGAGGTACAT	4703
rs751062424	snp	C/T	1.66346e-05	0.00288393	intron-variant	NEB	GRCh38.p7	2:151618226	ATCAGAATTTTTAAA[C/T]TGTTCTGTGGTAACT	4703
rs751065117	snp	A/G	1.73682e-05	0.00294683	synonymous-codon	NEB	GRCh38.p7	2:151682716	TTCTAAGGACCCAAA[A/G]GGCACCCAGCCACAA	4703
rs751068542	snp	C/T	8.47853e-05	0.00651041	intron-variant	NEB	GRCh38.p7	2:151627246	GTATTACTGAAGTTG[C/T]TTTAACATGATTTCA	4703
rs751075730	in-del	-/AAAG	0.000262548	0.0114545	intron-variant	NEB	GRCh38.p7	2:151617486	ACAAAAAAAAAAAAA[-/AAAG]AGAGAGAGAGAGAGA	4703
rs751093136	snp	G/T	3.3129e-05	0.00406982	missense, intron-variant	NEB	GRCh38.p7	2:151627069	GTCACACTGGTAAAT[G/T]TCAGCTTGTCCGGAG	4703
rs751094658	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151487044	TTATGTATGCATGAA[A/G]TTGTGTGTGTGTGCG	4703
rs751098420	snp	C/G	1.65696e-05	0.00287828	intron-variant	NEB	GRCh38.p7	2:151631121	TGGCATCTTGGAGAA[C/G]CTTAAGGCAGCTAGG	4703
rs751108424	in-del	-/AT			upstream-variant-2KB	NEB	GRCh38.p7	2:151736079	TATACTTAATATGCA[-/AT]AGACATTTTTATGAA	4703
rs751111521	in-del	-/TTC	9.30362e-05	0.00681978	cds-indel, intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151499376	CCCTTTTCCAACGTT[-/TTC]TTTATACAACACCTG	4703
rs751124198	snp	C/T	1.6577e-05	0.00287893	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151525165	AGGGAAAACTTACAT[C/T]ACTTTGCTTCTTGGC	4703
rs751128054	snp	C/T	1.65669e-05	0.00287805	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151490038	GCAACTGAAGATGAT[C/T]GTTGTTGTGGGAGCT	4703
rs751128682	snp	G/T	1.91206e-05	0.00309192	intron-variant	NEB, RIF1	GRCh38.p7	2:151493463	AGGGAAGCCAAAAGA[G/T]CATCTAGGCATCAGA	4703
rs751129331	snp	A/C	2.15218e-05	0.00328031	missense	NEB	GRCh38.p7	2:151565559	GGAGGATCCACCACA[A/C]TTCTAAAGTTAGGAT	4703
rs751129598	in-del	-/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151503305	GGTTATTGTGGTAAA[-/T]TTTTTATGGGAAATA	4703
rs751142187	snp	A/T	1.69109e-05	0.00290778	synonymous-codon	NEB	GRCh38.p7	2:151541456	GCTTACCTGACTCTG[A/T]AGCTTCTGCCCTCGC	4703
rs751159312	snp	C/T	4.96816e-05	0.00498381	missense, intron-variant	NEB	GRCh38.p7	2:151640536	TTCCACTTCTCAAAG[C/T]CCTTCTTGTACTCCC	4703
rs751167749	snp	C/T	5.77895e-05	0.00537508	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151526228	ACGGCATGGCAGGTT[C/T]CTCTTTCCTTGACAT	4703
rs751181789	snp	A/C/G	3.31825e-05	0.00407313	intron-variant	NEB	GRCh38.p7	2:151692203	ATTCAAGTTAACAAT[A/C/G]ATTTGTCAAACAGTA	4703
rs751194502	snp	C/T	1.65592e-05	0.00287738	missense, intron-variant	NEB	GRCh38.p7	2:151640434	CACTGGTGCAGGTAG[C/T]TCTTGTAGTCCACAT	4703
rs751212315	snp	A/G	1.65891e-05	0.00287998	intron-variant	NEB	GRCh38.p7	2:151655803	GCTGTGTGGACGGCC[A/G]CTGTTCTCTGTACCT	4703
rs751222116	snp	C/T	2.02908e-05	0.00318512	intron-variant	NEB	GRCh38.p7	2:151662122	TGAAACACTGCATTA[C/T]TGAAAGACTTACTTC	4703
rs751223917	snp	C/G/T	4.97231e-05	0.00498593	missense, intron-variant	NEB	GRCh38.p7	2:151618310	TGTTTTTTGCCAGCA[C/G/T]CTGCTCCGGAGTGTC	4703
rs751224989	snp	A/T	0.000127498	0.00798328	intron-variant	NEB	GRCh38.p7	2:151560586	TCATGTTTTTGCTTT[A/T]CTTACATGGCTGGCC	4703
rs751228445	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151520818	GCAGTGAGTCAGGAT[C/T]GCACCACTGCACTCC	4703
rs751229526	in-del	-/TGT			intron-variant, cds-indel, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151498019	ACTGTTAGAACTCGG[-/TGT]TGTTATCCACACAAA	4703
rs751246882	snp	A/T	2.70435e-05	0.00367709	intron-variant	NEB	GRCh38.p7	2:151733111	TCAGTGTTTTTTTTT[A/T]AAATCTTACCTCCAC	4703
rs751252166	snp	A/C	1.66277e-05	0.00288333	intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151534369	ACAACTTCAAGGCTA[A/C]ACAAAAATGTCTCAA	4703
rs751256739	in-del	-/AGCAA	1.70901e-05	0.00292314	intron-variant	NEB	GRCh38.p7	2:151672702	AGGCAGAATTGGGTT[-/AGCAA]AGTCCTAGGCATTGA	4703
rs751269690	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151728463	GCATCAATATTATAA[A/G]AGATTTTCATTCCCT	4703
rs751269756	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151634422	GCTAAGGCAGGTGGA[C/T]CATGAGGTCAGGAGA	4703
rs751270076	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151643001	TTTTCAGGTCTAAAT[A/G]TCTTGTGTCAATAAG	4703
rs751280827	snp	A/G	2.2658e-05	0.00336578	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151496364	ATGTTTTCTTTGTAT[A/G]ACACCTGTGCGATGA	4703
rs751291481	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151682887	GCTTCCTTACTCCAG[A/G]CATTAAGGTTATTTT	4703
rs751303153	snp	C/T	3.38564e-05	0.00411425	intron-variant	NEB	GRCh38.p7	2:151687587	AAATGTCCCCAAGGC[C/T]ACCCTGTCCAGGTCC	4703
rs751304945	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151635477	TTTGGGAGCCTGAGG[C/T]AAGTGGATCACCTGA	4703
rs751332969	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151508946	TTTTTCTTTCATCAT[C/T]GCTTGTCACTGTCCT	4703
rs751345146	snp	A/G	6.60786e-05	0.0057476	intron-variant	NEB	GRCh38.p7	2:151565685	GGTAGGAGGACAGGC[A/G]TAGGTTAGAAGGAGA	4703
rs751346602	in-del	-/G	1.79053e-05	0.00299204	frameshift-variant	NEB	GRCh38.p7	2:151684830	ACATTGATGCTATCA[-/G]GGGGGTAGCTGTAAC	4703
rs751352182	snp	C/T	1.65745e-05	0.00287871	missense	NEB	GRCh38.p7	2:151655899	TGGAAGTTGCTCGGG[C/T]GCTGGCGGTATTTCT	4703
rs751353236	snp	A/G	6.6302e-05	0.00575731	intron-variant	NEB	GRCh38.p7	2:151679856	TGTCATTTAAGTACA[A/G]CTTAGAGACTGTGTT	4703
rs751361823	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151621262	ACAAATCTTTTACAC[A/G]TTATACATTAAATGA	4703
rs751363280	in-del	-/T	1.6821e-05	0.00290004	frameshift-variant	NEB	GRCh38.p7	2:151547649	CTCACTGACAGCCTC[-/T]TGTGTCTTCTTGACT	4703
rs751366549	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151554802	TTTGTAGTCTAGGAG[A/C]AATAGGCTATCCCAT	4703
rs751373246	snp	A/G	1.65644e-05	0.00287783	missense	NEB	GRCh38.p7	2:151687463	AGTGCAGCATCTTTG[A/G]ATCGTCATTAATGCT	4703
rs751375256	snp	C/G	2.27384e-05	0.00337175	intron-variant	NEB	GRCh38.p7	2:151552652	TTACTGTCCACTTAA[C/G]TTCCCCAGTGATCAC	4703
rs751381939	snp	A/G	6.63989e-05	0.00576151	intron-variant	NEB, RIF1	GRCh38.p7	2:151526881	GGAAGATGGCCCTGA[A/G]TGAGGTTAGGCATCA	4703
rs751387280	snp	G/T	1.6593e-05	0.00288031	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151492237	ATCTGTCACCACTGG[G/T]GTGAAGCAACCCTTG	4703
rs751389797	snp	A/G	1.66214e-05	0.00288278	intron-variant	NEB	GRCh38.p7	2:151546460	TGAGAGGCAAACACA[A/G]AAATATAGCTGGTCA	4703
rs751394716	snp	C/G/T	0.000182366	0.00954754	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151485804	GCATTCCGGTCCTGC[C/G/T]AGTCCTCTGCACAGT	4703
rs751406959	snp	C/T	1.86621e-05	0.00305462	intron-variant	NEB	GRCh38.p7	2:151619810	GCACAAAGGGCTATT[C/T]CCTGTTGTTCTTTCT	4703
rs751410886	snp	A/C	4.33736e-05	0.00465671	missense, intron-variant	NEB	GRCh38.p7	2:151646230	CAAGCTTCTCTATAA[A/C]GTCTCTAAAATAAGA	4703
rs751414365	snp	C/T	3.31208e-05	0.00406931	missense, intron-variant	NEB	GRCh38.p7	2:151633841	TTCTCAAAGTCCTTT[C/T]TGTACTCCCTGTCAC	4703
rs751417359	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151656806	GTACTTTGCTGTTAG[C/T]GCTAAAGAGGCCTTT	4703
rs751428967	snp	G/T	1.6593e-05	0.00288031	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151612213	CAGGGCATTATTCTT[G/T]GCTAGGACAATTTCC	4703
rs751429773	snp	C/T	1.72743e-05	0.00293885	intron-variant	NEB	GRCh38.p7	2:151656477	ATACTGTGAAGAAAA[C/T]ATGAGTTTTTACACA	4703
rs751440474	snp	C/T	1.66846e-05	0.00288826	missense, intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151496972	TGATTGTGTTTGACT[C/T]TCTCCATCTCAGGAG	4703
rs751450878	snp	A/C	1.65647e-05	0.00287786	missense, intron-variant	NEB	GRCh38.p7	2:151629571	TGGAGGCCTTGGCAG[A/C]CACGATGGGGATGGC	4703
rs751455983	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151529001	TCCATGGCATGGGAT[A/G]AAGCTTCCTTTGCTC	4703
rs751456572	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151541748	GTGTCAAAACAAGAG[A/T]CATTCTCTAGCCTGT	4703
rs751462080	in-del	-/G	1.68556e-05	0.00290302	intron-variant	NEB, RIF1	GRCh38.p7	2:151490117	TATAAGAAGAAAAAT[-/G]GCTAGGTATCCTTTA	4703
rs751469627	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151670761	TTCATATGTATAATG[C/T]GTATCTGCTTATGAA	4703
rs751470649	snp	C/G	8.3944e-05	0.00647804	missense	NEB	GRCh38.p7	2:151697631	TTTTGTCTTTTCATA[C/G]TTTTCCTTGTATAGT	4703
rs751474807	snp	A/G	1.66114e-05	0.00288192	missense, intron-variant	NEB	GRCh38.p7	2:151650198	CTATTTTTGGCATTT[A/G]TCTTTGCCAGAACTA	4703
rs751475190	snp	A/C	3.31263e-05	0.00406965	missense, intron-variant	NEB	GRCh38.p7	2:151643184	TTGTTTTTTGCCAAA[A/C]CCATTGGTATGGAAT	4703
rs751475228	snp	A/G	1.70842e-05	0.00292264	intron-variant	NEB	GRCh38.p7	2:151694639	AAGATTCTGGACAAA[A/G]AAATTCAGCAAAGGA	4703
rs751477515	snp	C/T	2.89247e-05	0.00380283	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151513686	TCCAGGTCTCGCTTA[C/T]ATTCTTTCTATAGTA	4703
rs751483486	snp	A/G	9.94069e-05	0.00704937	missense	NEB	GRCh38.p7	2:151553919	CGCAGGCGGTAATCA[A/G]TCTCACTGACTTTCT	4703
rs751485151	snp	A/G	2.16842e-05	0.00329266	missense	NEB	GRCh38.p7	2:151562621	CATACATCACTCAAG[A/G]TCTCCTGGGCGTTTC	4703
rs751494785	snp	A/G	1.65839e-05	0.00287953	missense	NEB	GRCh38.p7	2:151663816	AGGCTCCGGAAGCCA[A/G]TGTGTTTCCCTTTGG	4703
rs751519609	snp	C/T	3.32066e-05	0.00407458	synonymous-codon	NEB	GRCh38.p7	2:151663734	TTTCTCATATCCCTT[C/T]TTGTATTCCCGGTCT	4703
rs751540631	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151554763	GTTGCCTACAGTATT[A/C]AGTACAGTAACATGC	4703
rs751546666	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151543410	TTCATGTTACTATTG[A/G]AAGAGATAAACTAAA	4703
rs751551042	snp	C/T	4.97121e-05	0.00498534	intron-variant	NEB	GRCh38.p7	2:151679909	CAGCCCGTGAGTCCA[C/T]CCACGCACCTCACTG	4703
rs751564866	snp	C/G	3.14936e-05	0.0039681	intron-variant	NEB	GRCh38.p7	2:151642891	GAAACAGAAAAACAT[C/G]ACTGGTATAGGCCAG	4703
rs751567546	snp	G/T	1.65789e-05	0.0028791	missense	NEB	GRCh38.p7	2:151538162	ATGTCATCTGTGACT[G/T]TGCGATGATAGACAA	4703
rs751570070	snp	A/G	3.16862e-05	0.00398021	intron-variant	NEB	GRCh38.p7	2:151671279	TGGAGAATATTCAAG[A/G]GATGTTTCTGGGATC	4703
rs751571184	in-del	-/CTTT			intron-variant	NEB, RIF1	GRCh38.p7	2:151521615	TGAGAATAAAATCTG[-/CTTT]TTTTAGAAGCATACT	4703
rs751592907	snp	A/G	1.65949e-05	0.00288048	intron-variant	NEB	GRCh38.p7	2:151610665	AAATAAGAGTGTTTG[A/G]GGAAGGTAATAGGCC	4703
rs751597129	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151689889	CATTCTCCTCTTTAC[C/T]AATTGGGTATGAGCT	4703
rs751597547	in-del	-/AG	1.66179e-05	0.00288248	intron-variant	NEB, RIF1	GRCh38.p7	2:151524644	GAAAATGTTTACTCA[-/AG]AGAGAGAGGCTTTTT	4703
rs751602407	snp	A/G/T	9.99663e-05	0.0070693	missense	NEB	GRCh38.p7	2:151666385	TTGGCTTTCTCGTAG[A/G/T]CCTCCTTATATTTGC	4703
rs751613683	snp	C/T	0.000347725	0.0131811	missense, intron-variant	NEB	GRCh38.p7	2:151633917	CTTCAATGTTCCGGG[C/T]TCCAATATGGTGGCC	4703
rs751615290	snp	C/T	1.65608e-05	0.00287752	missense	NEB	GRCh38.p7	2:151563899	GTGTAGCCATAGGCC[C/T]TGGTGCCCTCCCACG	4703
rs751617027	snp	C/T	6.77897e-05	0.00582153	intron-variant	NEB, RIF1	GRCh38.p7	2:151491653	CTAAATGGTGATGTT[C/T]ATGTTGTAAGCCTTT	4703
rs751617454	snp	A/C	5.22411e-05	0.00511056	intron-variant	NEB	GRCh38.p7	2:151654141	TTATTCTGTCTATAT[A/C]AAGAATATCAATAGA	4703
rs751623331	snp	A/T			upstream-variant-2KB	NEB	GRCh38.p7	2:151736021	CCTTCTTAGTCATTT[A/T]TAAGTTTCAGATATT	4703
rs751624391	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151691087	AGCCTTACACAGTGA[A/C]TCTTTAGTCAACTTG	4703
rs751642040	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151704856	GGAGCTGTAGACCGG[A/G]GCTGTTCCTATTCGG	4703
rs751650751	snp	A/C/T	4.97033e-05	0.00498494	missense, intron-variant	NEB	GRCh38.p7	2:151610554	CCTTGGCACTTTTGA[A/C/T]GGAAATAGCATCTGC	4703
rs751651573	snp	C/T	3.31038e-05	0.00406827	intron-variant	NEB, RIF1	GRCh38.p7	2:151518937	ATGGGTAAAACAAGC[C/T]GTTTCTGGAGCAAAT	4703
rs751657802	snp	C/T	3.32419e-05	0.00407675	missense	NEB	GRCh38.p7	2:151671175	CCTCCAGGGAACCAA[C/T]AGGGATCCATCCGAT	4703
rs751661672	snp	A/T	3.53938e-05	0.00420662	intron-variant	NEB	GRCh38.p7	2:151633620	AGTTTAAATTATTTC[A/T]ATGCACAGCTCCATT	4703
rs751665091	snp	A/T	0.000132494	0.00813815	synonymous-codon	NEB	GRCh38.p7	2:151697419	GCTGCCTACATAATG[A/T]CCCAAAATATCTTTT	4703
rs751677106	snp	A/G	5.02635e-05	0.0050129	intron-variant	NEB	GRCh38.p7	2:151692003	AAATAGATCATGATT[A/G]TTATGGCTCTCAAAC	4703
rs751677850	in-del	-/A	0.000235363	0.0108456	intron-variant	NEB	GRCh38.p7	2:151643109	AGTGTTTCCATAAAC[-/A]AAAAAAATTAATAAC	4703
rs751680308	snp	A/G	5.89675e-05	0.00542957	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151494213	ATCTCAGGAGTGACA[A/G]GGGTTGCGGTGGCTT	4703
rs751681905	snp	C/T	8.96355e-05	0.006694	missense	NEB	GRCh38.p7	2:151684873	GCTTATAATCAACGT[C/T]GCTGGCAATTGCCTG	4703
rs751687245	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151676638	ATTGTTCATTCCTTT[C/T]CTACTGCTGTTATAT	4703
rs751690109	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151643050	CCACATTAGTACCAA[A/G]CAAAGGAATCAAAAA	4703
rs751696276	in-del	-/C	3.31494e-05	0.00407107	frameshift-variant	NEB	GRCh38.p7	2:151655841	GGTATGTGCATTCTG[-/C]TTGGCAAGCACCATG	4703
rs751696754	snp	A/G	8.29497e-05	0.00643956	intron-variant	NEB	GRCh38.p7	2:151617350	GTTCATTACAAGATC[A/G]ACAGTTTACTTACAT	4703
rs751699429	snp	C/T	1.66507e-05	0.00288532	missense	NEB	GRCh38.p7	2:151717456	TTGGCAAATTCTATA[C/T]CTGGAGGATCAGCCA	4703
rs751720097	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151549545	TTGAACCTTGAGGGT[A/G]AGACTGGAGGATTAG	4703
rs751724804	snp	A/G	0.000152981	0.00874455	missense	NEB	GRCh38.p7	2:151549692	GAGGAGTGTCACCTG[A/G]AAGTCTATATCCAGT	4703
rs751729671	snp	A/G	1.67374e-05	0.00289282	intron-variant	NEB, RIF1	GRCh38.p7	2:151492064	TACCCCCTCACTTAA[A/G]GTTAATCCCCTCCCC	4703
rs751732546	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151715133	ATGCTTTCAAAGTAC[A/C]CAACACTGTCACCTT	4703
rs751747575	snp	A/G	3.31362e-05	0.00407026	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151631293	CACATCCATAGACCC[A/G]ATGGGGACCCAGCCA	4703
rs751750770	in-del	-/CT			intron-variant	NEB	GRCh38.p7	2:151706241	ACAAAGAAAAGATAA[-/CT]AACCCACACAGACAG	4703
rs751756810	in-del	-/A	0.000105357	0.00725725	intron-variant	NEB, RIF1	GRCh38.p7	2:151526310	TCTGCTGGATATCCT[-/A]ACATATTTTTATTAC	4703
rs751767468	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151616729	AAACAGTATTTATTA[C/T]TGTCATCATAATATA	4703
rs751774625	snp	G/T	5.00872e-05	0.00500411	intron-variant	NEB	GRCh38.p7	2:151644609	CATTTTGGGAAATAC[G/T]GTTCCCCATAGACAA	4703
rs751776632	snp	A/C	1.72024e-05	0.00293273	splice-donor-variant, intron-variant	NEB	GRCh38.p7	2:151642572	TTTCCAAGTATACTT[A/C]CTTCACTTGCAATAT	4703
rs751778176	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151732173	ACTGCCTCCAAGTGC[C/T]TTAGGCATTTGGAGA	4703
rs751782241	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151630052	TACGTATAAAAATAT[A/T]TTTTTATTCATTTTT	4703
rs751783628	snp	A/G	5.3638e-05	0.00517843	intron-variant	NEB	GRCh38.p7	2:151666056	TTCCTCCCACCCATT[A/G]GAAATGGATAACAAC	4703
rs751787450	snp	A/G	1.67584e-05	0.00289464	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151519037	GTCAGTCACGGGTTT[A/G]TGAAGTTTCTTCAGG	4703
rs751799971	in-del	-/CTCC			intron-variant	NEB	GRCh38.p7	2:151714395	AGTAATCATTTCTTG[-/CTCC]CTCCTCAACAGAATT	4703
rs751812161	snp	A/G	1.65682e-05	0.00287817	missense, intron-variant	NEB	GRCh38.p7	2:151614341	CAGGCAGGCAGGTCC[A/G]TTCATGCAGGGGATG	4703
rs751820717	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151696886	TAGACTGTAGTTTGA[C/G]AGGTGCTCTTATATC	4703
rs751831934	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151573617	CTTATAGAGCTGTTT[C/G]GCACATGGTGAGGAA	4703
rs751842194	snp	C/T	3.49773e-05	0.00418179	missense	NEB	GRCh38.p7	2:151561051	TGTCATAATCCACTG[C/T]TTCTAGAACTGTTGT	4703
rs751842742	snp	A/T	0.000460134	0.015161	intron-variant	NEB	GRCh38.p7	2:151546025	AAAAAAAAACAGAAA[A/T]ACAAGTTGATTAATC	4703
rs751844098	snp	A/T	4.24737e-05	0.00460815	missense	NEB	GRCh38.p7	2:151565092	GGAGATATGTGGTGT[A/T]TCTGGTGAAAACGTA	4703
rs751847160	snp	A/G	0.000313067	0.0125074	intron-variant	NEB	GRCh38.p7	2:151537096	GTACAGGTATATGTC[A/G]AATGGATGAGGCCAA	4703
rs751860529	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151548466	GTAAACAAGGACCAA[C/G]ATTACATTTCTCCAA	4703
rs751865750	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151631413	GGTAAATATGCAAAT[A/G]GAATCAGTAATAAAG	4703
rs751868241	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151571165	CATGCGCCACCAGGC[C/T]CAGCTAATTTTGTAT	4703
rs751870182	snp	A/G	3.35492e-05	0.00409554	missense	NEB	GRCh38.p7	2:151537919	GGAAATGCTCTGGAC[A/G]ATCAGGAATGGACCT	4703
rs751872533	snp	C/T	1.65756e-05	0.00287881	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151529211	TTTCTGGAACTTACA[C/T]TGGTGTTGACTTTGT	4703
rs751875993	snp	C/T	2.73228e-05	0.00369603	missense	NEB	GRCh38.p7	2:151684965	TTTTCATAATCTTTT[C/T]GATATTCGCGCTGTG	4703
rs751877532	snp	G/T	2.91244e-05	0.00381593	intron-variant	NEB	GRCh38.p7	2:151678229	TTAAAATGTAGTTTT[G/T]AGGGCTTTACTAAAC	4703
rs751893167	snp	C/G/T	3.35978e-05	0.00409853	intron-variant	NEB	GRCh38.p7	2:151694484	CAAGAGGAAATGTCC[C/G/T]CGAAGCCAGCCTGTC	4703
rs751900587	snp	C/T	1.7184e-05	0.00293117	intron-variant	NEB	GRCh38.p7	2:151674448	TCAAAAAGGCAAACA[C/T]CTAAACTTCACCTAA	4703
rs751919085	snp	A/G	1.69934e-05	0.00291486	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151636263	GGCCTTGGCCGCCAC[A/G]ATGGGGATGGCGTCG	4703
rs751925793	snp	C/T	1.84266e-05	0.00303528	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151527541	TCGGTCAGGAGTCCA[C/T]TTCCAGTGGGCTTTG	4703
rs751935179	snp	C/T	1.6591e-05	0.00288015	missense	NEB	GRCh38.p7	2:151656248	GCTTGTAGTTAGTGT[C/T]GGTGATGTTGGCTTG	4703
rs751938843	snp	A/G	0.000165703	0.00910077	missense, intron-variant	NEB	GRCh38.p7	2:151619648	CTTTCTTGTACTCAC[A/G]GTCACTCTGCACTTT	4703
rs751939044	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151650463	GCATTACAAACAGAT[A/G]CATTTTAGATTTTCA	4703
rs751944054	snp	C/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151492841	GTAGGGAATTTGAAA[C/G]AACTGTCCTTTAAAA	4703
rs751951834	snp	C/T	1.65765e-05	0.00287888	synonymous-codon	NEB	GRCh38.p7	2:151725549	TTTCTCAAACTTCTC[C/T]TTGTATTTATTCTGA	4703
rs751957350	snp	C/T	3.31647e-05	0.00407201	missense	NEB	GRCh38.p7	2:151567250	TGGTGCAAGTAATTA[C/T]GATAATCAATATCAC	4703
rs751961393	in-del	-/A			intron-variant	NEB	GRCh38.p7	2:151668159	ATAACAAAGCAACAG[-/A]AAGGTAATGCTTTGA	4703
rs751972598	snp	C/G	1.72788e-05	0.00293923	missense, intron-variant	NEB	GRCh38.p7	2:151642670	TTCTTCTAGGCCAAG[C/G]TTATACAATTTCTAA	4703
rs751976783	snp	A/G	0.000364287	0.0134911	synonymous-codon	NEB	GRCh38.p7	2:151694380	GGGATCGTCATTAAT[A/G]CTGAGGACTCCAATC	4703
rs751984756	snp	A/G	0.000100842	0.00710006	intron-variant	NEB	GRCh38.p7	2:151670986	CAGACACGTGTGGTT[A/G]TTTACGGGCAAATCA	4703
rs751988475	snp	C/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151516395	AACTGGCCATGTCAT[C/G]GGCAGAGCTTGTGTT	4703
rs751994032	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151704916	ATTAAGAAACCAATA[A/T]GCCACCTCTGACCAC	4703
rs752014573	snp	A/G	1.88667e-05	0.00307132	missense	NEB	GRCh38.p7	2:151570142	TGGTCGGGCATGCAG[A/G]TCCACTGGTGCAGGT	4703
rs752016512	snp	C/G	9.16548e-05	0.00676897	intron-variant	NEB	GRCh38.p7	2:151690668	GCATGTAAATGCTTA[C/G]ATTTTAAATGAGCAA	4703
rs752020105	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151652352	CACCTCAGCCTCCCA[A/G]GTAGCTGAGACTCCA	4703
rs752021639	snp	A/G	6.63967e-05	0.00576142	intron-variant	NEB	GRCh38.p7	2:151697519	TTCTTTTTTTAACAG[A/G]AAGAGTGACAGTAGG	4703
rs752028559	snp	C/T	4.97063e-05	0.00498505	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151524616	CTTTTCTGTAAGCGA[C/T]CTTTATTGGGGAAGA	4703
rs752037296	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151524068	TGTCACATAAAGATA[A/G]TTAAGCACACAGACA	4703
rs752039321	snp	G/T	2.03097e-05	0.0031866	intron-variant	NEB, RIF1	GRCh38.p7	2:151512693	CTTCCATTCTTTCAT[G/T]ATTGGGGTTTATGAG	4703
rs752051506	snp	A/G	5.59394e-05	0.00528834	intron-variant	NEB	GRCh38.p7	2:151709799	TGAAGAACTGCTGTG[A/G]AAATGAACTATGCAA	4703
rs752056199	in-del	-/AT	2.12454e-05	0.00325918	intron-variant	NEB	GRCh38.p7	2:151610171	TTTAAAACCATGCTC[-/AT]GTGCTGACAATTACA	4703
rs752086781	snp	C/T	3.31214e-05	0.00406935	missense	NEB	GRCh38.p7	2:151672535	GTATGGTAGCTGGTT[C/T]TGGTGTTCTCATAGT	4703
rs752089716	snp	C/T	1.73601e-05	0.00294614	missense, intron-variant	NEB	GRCh38.p7	2:151609850	TTGCTTGGATAATGT[C/T]GTTTTGATCCGGCAT	4703
rs752094861	snp	C/T			missense	NEB	GRCh38.p7	2:151695579	CATAAGGAACTTACA[C/T]CACTCAAGTTATAGG	4703
rs752095965	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151557689	TCAAGTCAGCTTCAT[C/T]ACTGGGATGCAAGCC	4703
rs752098313	snp	A/G	4.98244e-05	0.00499096	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151650667	GTTCTTGTAGTCCAC[A/G]TCACTAACCAACTCC	4703
rs752102535	snp	A/G	1.65888e-05	0.00287996	missense	NEB	GRCh38.p7	2:151540768	CAGCGTGATGATGGG[A/G]TCTCTCTTTGGTGGC	4703
rs752103155	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151535412	CTTTACCTGCCTGGT[A/G]TTGTCACCCGCAGGG	4703
rs752113075	snp	A/G	8.31179e-05	0.00644609	missense	NEB	GRCh38.p7	2:151567359	GATAGTCCTCTTTGT[A/G]TAGTCTCTCATTCTG	4703
rs752114805	snp	A/G	3.31466e-05	0.0040709	synonymous-codon	NEB	GRCh38.p7	2:151656333	CTTTGTGTTCTCATA[A/G]TTTTTCTTGTACTCC	4703
rs752127208	snp	A/G	1.79968e-05	0.00299968	intron-variant	NEB	GRCh38.p7	2:151650567	ATTGGATTTAATAGA[A/G]ACTGACCTCACTTTG	4703
rs752127302	snp	A/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151511672	GCAGACTCCTGACCA[A/T]CACTGACAATCGTTC	4703
rs752140285	snp	G/T	2.00142e-05	0.00316334	missense, intron-variant	NEB	GRCh38.p7	2:151636325	CTTCATTAGCAAGTT[G/T]GTACAGACTCTAAAT	4703
rs752141396	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151725440	TCTCCTTTATTTCAG[C/T]AATGCAGCCCACCTC	4703
rs752150326	snp	C/G	1.65718e-05	0.00287848	missense, intron-variant	NEB	GRCh38.p7	2:151627160	TAGACCCAATGGGGA[C/G]CCAGCCAATGCCTCT	4703
rs752157470	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151521178	CCCCAACTTGACACA[C/T]CCAGCACAACAGACA	4703
rs752162339	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151649671	CCTATTATGTGCTAG[A/C]TACTGGTGTCAGAGC	4703
rs752170910	snp	C/T	2.18558e-05	0.00330566	intron-variant	NEB	GRCh38.p7	2:151553795	GCCGTGGGGCGGGGC[C/T]GTGGAGGGGTACTTC	4703
rs752174970	snp	A/C/T	0.000399644	0.0141306	synonymous-codon, missense	NEB	GRCh38.p7	2:151669072	TTGAATAAACTGAGG[A/C/T]AATTCAGGGTCAATA	4703
rs752178904	snp	A/C	1.65817e-05	0.00287933	missense	NEB	GRCh38.p7	2:151677998	CCTGGGCTTTCTTAG[A/C]CGCCACGACATTGAA	4703
rs752185026	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151522187	TAATTGTATTTGAAG[C/T]TTAAGATCTAATTTT	4703
rs752193330	snp	C/T	1.68457e-05	0.00290216	missense, intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151497026	CCCATGTTTTCTTTG[C/T]ATAACACCTGTGCGA	4703
rs752193365	snp	C/T	1.66067e-05	0.00288151	missense	NEB	GRCh38.p7	2:151678054	GACTTTGTCTTCTCA[C/T]AGTCTTTTTTATACT	4703
rs752202907	snp	C/G	3.98383e-05	0.00446291	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151526942	TATTAAAGTATTCCT[C/G]AGGGCGAGCACCGTG	4703
rs752227497	snp	C/T	6.65082e-05	0.00576625	missense	NEB	GRCh38.p7	2:151692305	GTTGATATTTTGGGG[C/T]CTCACAGTAATTCAT	4703
rs752233745	snp	A/G	9.94184e-05	0.00704977	missense	NEB	GRCh38.p7	2:151554963	CAACTCGGAGGCACC[A/G]TGCTGTGTTCGGATC	4703
rs752233898	snp	G/T	1.67178e-05	0.00289113	intron-variant	NEB	GRCh38.p7	2:151627854	AATAAAGGTGGTCAT[G/T]TCAAAAATAAAAATG	4703
rs752237252	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151720235	GGAAAACATGATAAG[C/T]AGATTAAGAAGGACA	4703
rs752241986	snp	G/T	1.65825e-05	0.00287941	intron-variant	NEB	GRCh38.p7	2:151562217	CTTTATACACATTCT[G/T]CAAGAAAGAGAGAAC	4703
rs752246621	in-del	-/T	1.65756e-05	0.00287881	frameshift-variant, intron-variant	NEB, RIF1	GRCh38.p7	2:151513677	ACTTCCAGTTCCAGG[-/T]CTCGCTTATATTCTT	4703
rs752267876	snp	G/T	1.65622e-05	0.00287764	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151518326	CACTTACTATACTCT[G/T]TAATTCTGTGGCCTC	4703
rs752269554	snp	A/G	1.66106e-05	0.00288184	synonymous-codon, nc-transcript-variant, intron-variant	NEB, RIF1	GRCh38.p7	2:151506250	TGAGACATCCTCTTT[A/G]TATAAAACCTGGGCA	4703
rs752270361	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151649245	CAGGTCAGCATTTAC[C/T]ATACATTCTGGAAAT	4703
rs752283693	in-del	-/ATGAACCATTGTCTTCAAACTT	1.65883e-05	0.00287991	intron-variant	NEB	GRCh38.p7	2:151692035	ATGTCACTGTGAGGC[-/ATGAACCATTGTCTTCAAACTT]ACATCACTGTTTTGA	4703
rs752285938	snp	C/T	3.28682e-05	0.00405377	missense	NEB	GRCh38.p7	2:151547454	ATGTCTCCCACATAG[C/T]GGCAATGGATCACTT	4703
rs752288259	snp	A/G	3.70343e-05	0.004303	intron-variant	NEB	GRCh38.p7	2:151724817	GCAGAGGTGATGCAC[A/G]TGCTACTGAGTACCC	4703
rs752295097	snp	A/G	2.152e-05	0.00328017	intron-variant	NEB	GRCh38.p7	2:151565704	GTTAGAAGGAGAATA[A/G]GCTTTGCGTACCTGA	4703
rs752314976	snp	G/T	1.65751e-05	0.00287876	missense	NEB	GRCh38.p7	2:151697227	CCTTTGCCTCTGTCT[G/T]CTTCGTATTCTGCTT	4703
rs752318455	snp	A/G	8.28645e-05	0.00643625	missense, intron-variant	NEB	GRCh38.p7	2:151618318	GCCAGCACCTGCTCC[A/G]GAGTGTCCGTTATAC	4703
rs752326827	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151669967	ACTCAGCAGAGGTAC[C/T]GCATGTGGGAGTTCA	4703
rs752327839	snp	C/T	9.93591e-05	0.00704767	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151633870	ACTCTGGATCTTGGC[C/T]ACGTGCATGGACCAC	4703
rs752328965	snp	C/T	4.98418e-05	0.00499183	missense	NEB	GRCh38.p7	2:151656014	CATTGTAATCTTGCT[C/T]ATATTCATTCTATAA	4703
rs752331021	snp	A/C			intron-variant	NEB, RIF1	GRCh38.p7	2:151509980	CCAACTCAAAATTAC[A/C]AAGTTTTTCAGAGCT	4703
rs752334619	snp	C/T	9.70662e-05	0.00696589	missense	NEB	GRCh38.p7	2:151570552	GGGATGGCATCCAGC[C/T]GGACATCACAGCCCG	4703
rs752338827	snp	A/T	1.65616e-05	0.00287759	missense, intron-variant	NEB	GRCh38.p7	2:151633934	CCAATATGGTGGCCA[A/T]GTTGCTTGCAGTAAC	4703
rs752344851	snp	C/T	2.14742e-05	0.00327668	missense	NEB	GRCh38.p7	2:151565789	ATCCAGCCAATGCCT[C/T]GGAGCCACTCCAGGT	4703
rs752349680	snp	C/T	8.28768e-05	0.00643673	missense	NEB	GRCh38.p7	2:151655905	TTGCTCGGGTGCTGG[C/T]GGTATTTCTGATCAC	4703
rs752349894	snp	A/C	6.22297e-05	0.00557772	intron-variant	NEB	GRCh38.p7	2:151692422	ATCTCATAAAGTAAA[A/C]GTCATTCATGTCTTT	4703
rs752351483	snp	C/T	6.65314e-05	0.00576726	intron-variant	NEB	GRCh38.p7	2:151569407	ATGAGTTCAGCAACC[C/T]TGGTCATGTGGTCCT	4703
rs752364121	snp	A/G	1.67595e-05	0.00289473	intron-variant	NEB, RIF1	GRCh38.p7	2:151527038	CTGTGATAGAAGAAA[A/G]GCAGAAGAAAAGGGA	4703
rs752372235	snp	G/T	1.66932e-05	0.002889	missense	NEB	GRCh38.p7	2:151666388	GCTTTCTCGTAGGCC[G/T]CCTTATATTTGCACT	4703
rs752379641	snp	C/T	1.65927e-05	0.00288029	missense, intron-variant	NEB	GRCh38.p7	2:151650217	TTGCCAGAACTATAT[C/T]CATGGCATCAGGAAT	4703
rs752396426	in-del	-/AC	1.69654e-05	0.00291246	intron-variant	NEB	GRCh38.p7	2:151548455	ATCAATGATGGGTAA[-/AC]AAGGACCAACATTAC	4703
rs752399918	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151720345	GCATTCTGCAAACAA[C/T]AGCTTGCTTAGGGCT	4703
rs752409761	snp	A/C	1.6894e-05	0.00290633	missense	NEB	GRCh38.p7	2:151695585	GAACTTACATCACTC[A/C]AGTTATAGGCATTGA	4703
rs752420000	snp	A/G	1.83768e-05	0.00303118	intron-variant	NEB	GRCh38.p7	2:151680042	AAGAGAAAAAAATGC[A/G]TAAACAAACAAATAA	4703
rs752425545	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151541940	AATTAAGCCTTTTCC[A/G]GTCTCTAGCCAATGG	4703
rs752431335	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151530242	TGGAGACATACCTAG[C/T]AAGTTTTGGTATATG	4703
rs752431957	snp	C/T	1.65864e-05	0.00287974	missense, intron-variant	NEB	GRCh38.p7	2:151640633	CACCAATGTGGTGGC[C/T]GAGCTGCTTACGATA	4703
rs752432007	in-del	-/GTA	1.6599e-05	0.00288084	intron-variant	NEB	GRCh38.p7	2:151562248	AATGAAATGTGGAAG[-/GTA]TTCTGAATTTACAAT	4703
rs752432245	in-del	-/AAAG			intron-variant	NEB	GRCh38.p7	2:151545590	CAAAAAAAAAAAGAA[-/AAAG]AAAGGTCTTTCTAAT	4703
rs752432423	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151624688	GTACTTAAATTTTTC[A/G]GTGCTCTCAAACTGA	4703
rs752435891	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151725691	AGCTTTCTTTTTGTC[C/T]CCTACCCCAACTCTC	4703
rs752442261	snp	C/T	3.92411e-05	0.00442933	missense	NEB	GRCh38.p7	2:151687712	TGGCTTTGCTCTTCT[C/T]CCAGTCTTGCTTATA	4703
rs752462184	snp	A/G	1.65616e-05	0.00287759	missense	NEB	GRCh38.p7	2:151666293	TGTACTCACGATCAG[A/G]CTGGATTTTGGCCAC	4703
rs752467283	snp	A/G			missense	NEB	GRCh38.p7	2:151535734	AAATGCCTATTGATC[A/G]GAGAGTCGGCAACAT	4703
rs752469790	snp	C/T	0.000155003	0.00880212	intron-variant	NEB	GRCh38.p7	2:151707029	AAATGATAAAGTAAC[C/T]CTATGGGTTATTTTT	4703
rs752473638	snp	G/T	1.65611e-05	0.00287755	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151514329	CTACCTCATTGAGGA[G/T]TTGAGTGGCATTCTT	4703
rs752495462	snp	A/G	5.57864e-05	0.00528111	intron-variant	NEB, RIF1	GRCh38.p7	2:151513717	GCATTAAAAGAAAAA[A/G]AAAAGGTACCTAAAT	4703
rs752513954	snp	A/C	0.00270492	0.0366762	missense, intron-variant	NEB	GRCh38.p7	2:151640014	AAAGAGCCAATGGAC[A/C]CCCAGCCAATGCCTC	4703
rs752520601	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151577636	CCCAGGCTGGAGTGC[A/T]GTGGCAATCTCGGCT	4703
rs752529011	snp	C/T	1.67998e-05	0.00289821	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151492428	TCACCCGTCTCATCT[C/T]GGGGGTATCCAATAC	4703
rs752534636	snp	C/G	1.65916e-05	0.00288019	missense	NEB	GRCh38.p7	2:151568319	TGAAACCCATACCTG[C/G]TCCAGTATCCTAGCA	4703
rs752534946	snp	A/G	5.3111e-05	0.00515293	intron-variant	NEB	GRCh38.p7	2:151570611	AAGTTTCTGAAAAGG[A/G]GAAAAATAAGGTATC	4703
rs752536032	snp	C/T	0.000154811	0.00879667	intron-variant	NEB	GRCh38.p7	2:151607488	GGCTTTTACACTTCA[C/T]GTTCGTGCCACTTAC	4703
rs752536311	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151643360	GTACAAATTCTGAAA[G/T]TGCAAGTGACAAATT	4703
rs752540640	snp	A/G	3.23766e-05	0.00402334	missense	NEB	GRCh38.p7	2:151691892	TCCAGCTTCTTGATT[A/G]CTTCATATTCTTGTG	4703
rs752553797	snp	A/G	6.92161e-05	0.00588245	synonymous-codon	NEB	GRCh38.p7	2:151706893	TACGTCACTTAGGGC[A/G]TCTCCTGCTGCCTTC	4703
rs752562590	in-del	-/GTGTGG			intron-variant	NEB	GRCh38.p7	2:151638835	TGTGTGTGTGTGTGT[-/GTGTGG]GTTACCTGGTAGTAC	4703
rs752565808	snp	A/C	5.35131e-05	0.0051724	missense	NEB	GRCh38.p7	2:151547533	CTGATTTGTAGATCA[A/C]CTAAAGAAAAAAAAA	4703
rs752579656	snp	C/T	3.31252e-05	0.00406958	missense, intron-variant	NEB	GRCh38.p7	2:151643188	TTTTTGCCAAAACCA[C/T]TGGTATGGAATCCAT	4703
rs752582527	in-del	-/CT	6.14949e-05	0.0055447	frameshift-variant, intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151496970	CTTGATTGTGTTTGA[-/CT]CTCTCCATCTCAGGA	4703
rs752586147	in-del	-/T			intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151507120	TATCTTTAAAAAAAA[-/T]GTCTATGCACAATAA	4703
rs752591391	snp	C/T	2.04405e-05	0.00319685	intron-variant	NEB	GRCh38.p7	2:151612425	AATATTTATAGATGT[C/T]ACCTAGACGGCCTGG	4703
rs752592929	snp	A/G	0.5	0	intron-variant	NEB	GRCh38.p7	2:151603820	GAGTCAAAGTTGCCC[A/G]TAAGAGTTTGATGCT	4703
rs752593789	snp	A/C			intron-variant	NEB, RIF1	GRCh38.p7	2:151516818	AAAAGAATCATTGAC[A/C]AGAGCCAGCTGAGAG	4703
rs752598891	snp	C/T	5.60135e-05	0.00529184	missense, intron-variant	NEB	GRCh38.p7	2:151616066	TCCAGACGCAAGTCA[C/T]AGCCTTCCTTCTTGG	4703
rs752603296	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151530140	CTAGTGTCAGGCACA[C/T]AGACAATATTTGATG	4703
rs752606341	snp	G/T	3.31279e-05	0.00406975	missense, intron-variant	NEB	GRCh38.p7	2:151629577	CCTTGGCAGCCACGA[G/T]GGGGATGGCGTCACT	4703
rs752609796	snp	C/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151499747	TTTTCTCTACAAAAA[C/G]CGTTTGTCTTACGGT	4703
rs752616176	in-del	-/GAAA			upstream-variant-2KB	NEB	GRCh38.p7	2:151734973	AGTGAAGTTAAAGGT[-/GAAA]GAAAATATTTGACAA	4703
rs752626000	snp	C/T	1.65787e-05	0.00287907	missense	NEB	GRCh38.p7	2:151554933	TGACCGTACTTACAT[C/T]GATGTTAAGCTTGCC	4703
rs752643338	snp	C/T	2.04346e-05	0.00319639	intron-variant	NEB	GRCh38.p7	2:151695686	TTTGTAATTTAACTA[C/T]GACAGAGAGAGAACC	4703
rs752650720	snp	C/G	1.89579e-05	0.00307873	intron-variant	NEB, RIF1	GRCh38.p7	2:151512718	TATGAGTGATGGCAT[C/G]ACGAATGTCCTTACC	4703
rs752655488	snp	A/G	3.31653e-05	0.00407204	intron-variant	NEB	GRCh38.p7	2:151659033	TCAAATCTGCTGGAG[A/G]GAAAGATGACAACAG	4703
rs752660824	snp	A/T	1.66579e-05	0.00288595	missense	NEB	GRCh38.p7	2:151727857	GAAGTTTCTGATTGC[A/T]CATAGTCAGATGTCC	4703
rs752681778	snp	G/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151504812	ACCTGATATTTCAGG[G/T]GTGGGGGACACGTGC	4703
rs752691224	snp	A/G	4.14568e-05	0.00455266	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151531089	CCTTGTTGTATTCCA[A/G]TTTATAAAGGATCTG	4703
rs752706153	snp	C/T	1.662e-05	0.00288266	intron-variant	NEB	GRCh38.p7	2:151687412	ACAGATTCACAAAGA[C/T]ACTCACATCACTCTG	4703
rs752706161	in-del	-/ATAAT	0.000161577	0.00898679	intron-variant	NEB	GRCh38.p7	2:151669173	ATATCATTAGCTGAC[-/ATAAT]ATAAATTTCATCAAG	4703
rs752707527	snp	A/G	1.66288e-05	0.00288343	intron-variant	NEB, RIF1	GRCh38.p7	2:151485943	GATTTTCTATTCGTG[A/G]GGATGGAAAAGGGGA	4703
rs752709295	snp	C/T	1.6563e-05	0.00287771	missense	NEB	GRCh38.p7	2:151666178	TATGACTGTCTGTAG[C/T]TGGCGTTGGTGGCAA	4703
rs752711370	snp	A/G	1.68091e-05	0.00289901	synonymous-codon	NEB	GRCh38.p7	2:151663569	TTGAATCTGCATCAT[A/G]TTTTTGGCCAATTCA	4703
rs752728924	snp	C/G	5.08014e-05	0.00503965	intron-variant	NEB, RIF1	GRCh38.p7	2:151531120	AAAGATCAAAAAGCA[C/G]AAAGACATCATGTCA	4703
rs752735649	in-del	-/TGG			intron-variant	NEB	GRCh38.p7	2:151638838	GTGTGTGTGTGTGTG[-/TGG]GTTACCTGGTAGTAC	4703
rs752740238	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151640975	ATAAATTTCAGGAGA[C/T]TATGCTGCAATGACA	4703
rs752741921	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151564861	AGCTCAAAAGCACCA[C/G]CTGAATAAACGCTAT	4703
rs752742064	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151550715	CCATCACAGTTCACT[A/G]CATCCTTGACCTCCC	4703
rs752744680	snp	A/G	7.16153e-05	0.00598352	missense	NEB	GRCh38.p7	2:151664523	GCAATGTCTCTAGAG[A/G]CTCTTGCAGCCTTTA	4703
rs752753583	snp	C/T	1.66181e-05	0.00288249	intron-variant	NEB, RIF1	GRCh38.p7	2:151519655	ACAATTTTAGAAACA[C/T]ACCTCACTTGCAAGA	4703
rs752762618	snp	A/G	0.000101932	0.00713831	intron-variant	NEB	GRCh38.p7	2:151692463	AACTGAAGGGGCAAA[A/G]TTTATGTTTTCTCAC	4703
rs752766337	snp	C/T	3.32784e-05	0.00407898	intron-variant	NEB, RIF1	GRCh38.p7	2:151492078	AAGTTAATCCCCTCC[C/T]CCAACCCAGGCTCAG	4703
rs752771727	in-del	-/TGGAC			intron-variant	NEB	GRCh38.p7	2:151661733	ACAGGCATGTAATCT[-/TGGAC]TTTTCTTTGATCCCA	4703
rs752773707	snp	A/G	1.69332e-05	0.0029097	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151519051	TGTGAAGTTTCTTCA[A/G]GTCAGCCTTGTATTT	4703
rs752778244	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151517799	AAAGGTTTTAAAATG[A/G]TACACCTGCATAGGG	4703
rs752791822	snp	C/G	3.92704e-05	0.00443099	missense, intron-variant	NEB	GRCh38.p7	2:151642830	CTGGCATAATGTGGA[C/G]AGTGGTTTTATCTTT	4703
rs752800070	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151732761	CTATACAGATACTAA[A/G]AGACAGAGTTCCATT	4703
rs752801727	snp	A/G	3.31208e-05	0.00406931	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151627742	CTGGATCTTGGCCAC[A/G]TGCATGGACCACATC	4703
rs752809792	snp	A/G	1.66098e-05	0.00288177	missense	NEB	GRCh38.p7	2:151679731	CTTACGTCACTCGCC[A/G]CCTGCCTGGCAGCTT	4703
rs752810060	in-del	-/GA	4.96882e-05	0.00498414	intron-variant	NEB, RIF1	GRCh38.p7	2:151527599	AGCTGTTTTTAACAG[-/GA]GAGAAAGGAATCACT	4703
rs752812755	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151730656	TGTAAAACACTTTAT[G/T]CTTCCTTTTTCTTAT	4703
rs752814885	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151730914	ATTCTGCCTGTATGT[C/T]GTTACACATAGCAAC	4703
rs752819207	snp	C/T	0.000296604	0.0121743	missense, intron-variant	NEB	GRCh38.p7	2:151591409	GCATCTGCTCGCAGG[C/T]CATAACCAGTCATCT	4703
rs752821359	snp	A/T	4.50237e-05	0.00474445	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151491753	AAAAACCGAACCAGG[A/T]TTAGTACGCCAGACA	4703
rs752823702	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151716296	GGCGCCCGCCACCAC[A/G]CCTGGCTAATTTTTT	4703
rs752825848	snp	G/T	8.31958e-05	0.00644911	missense, intron-variant	NEB	GRCh38.p7	2:151610823	GTGTCTGGCATCACG[G/T]GGATGGAGGTTTTGT	4703
rs752826478	snp	A/G	3.36185e-05	0.00409977	intron-variant	NEB	GRCh38.p7	2:151694486	AGAGGAAATGTCCCC[A/G]AAGCCAGCCTGTCCA	4703
rs752828094	in-del	-/AAGT	2.89457e-05	0.00380421	intron-variant	NEB	GRCh38.p7	2:151545871	ATTGACTTCAATGAC[-/AAGT]AAAGCGTCCTTACCT	4703
rs752829395	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151631449	TTCTGTTTTCTATTC[A/G]TAGAAAACAAGCGCG	4703
rs752836728	snp	C/T	4.97187e-05	0.00498567	missense	NEB	GRCh38.p7	2:151656349	TTTTTCTTGTACTCC[C/T]GATCAGATTGCATCT	4703
rs752847889	snp	A/G	1.68835e-05	0.00290542	missense	NEB	GRCh38.p7	2:151672412	GTATGCTCAAGACTC[A/G]TGGCGTCAGGTAGGT	4703
rs752852239	snp	C/T	2.33861e-05	0.00341943	intron-variant	NEB	GRCh38.p7	2:151636341	GTACAGACTCTAAAT[C/T]TGGGGGAAAAAAAAT	4703
rs752857965	snp	A/G	1.67936e-05	0.00289767	intron-variant	NEB	GRCh38.p7	2:151644617	GAAATACTGTTCCCC[A/G]TAGACAAATATAGCA	4703
rs752862300	snp	G/T	2.02645e-05	0.00318305	intron-variant	NEB	GRCh38.p7	2:151553803	GCGGGGCCGTGGAGG[G/T]GTACTTCTTAAGTCA	4703
rs752863746	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151538806	ATCTTTGTGATATTT[C/T]AAGAGAAAACAGCTC	4703
rs752868147	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151505911	TCCAGGAAGGTTGGT[C/T]CTTTGACTGTACCGG	4703
rs752877760	snp	C/T	9.20429e-05	0.00678329	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151592088	CAGGGGAGTGTCAGC[C/T]GGCACGTTCACATTA	4703
rs752881790	snp	A/G	3.28272e-05	0.00405124	missense, intron-variant	NEB	GRCh38.p7	2:151646182	ATGTCAGGTGTATCA[A/G]GCATGATGTGGATCT	4703
rs752889625	snp	C/G/T	3.31177e-05	0.00406914	missense, intron-variant	NEB	GRCh38.p7	2:151627642	AGGTCTGGCACTTCT[C/G/T]GGCTAACACCACTCC	4703
rs752890513	snp	C/T	3.31301e-05	0.00406989	synonymous-codon	NEB	GRCh38.p7	2:151697434	TCCCAAAATATCTTT[C/T]AAGTAGGAATCTTTA	4703
rs752893483	snp	C/T	3.3157e-05	0.00407154	splice-acceptor-variant	NEB	GRCh38.p7	2:151723488	TCAGTGTACAGTTTC[C/T]AAATCAAAAAAGAGT	4703
rs752911349	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151492980	ATCCATTTCAGAGTA[C/T]TACCCATGTCATAAA	4703
rs752912604	snp	C/T	1.65638e-05	0.00287778	missense	NEB	GRCh38.p7	2:151679797	TCATATCCCTTCTTG[C/T]TCAAGTCTTTCAAGT	4703
rs752916632	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151659879	GCTACGTAGTATTTC[A/T]TTAGGAGGTATAATC	4703
rs752928207	snp	C/G	0.0002372	0.0108878	missense	NEB	GRCh38.p7	2:151567405	CTCAAACCAAACCAG[C/G]TTAGGATCATCTCTC	4703
rs752929929	in-del	-/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151515139	TCAGGCTGAGACACT[-/T]TGATGGGCCCCTCAC	4703
rs752930244	in-del	-/CTCC			intron-variant	NEB, RIF1	GRCh38.p7	2:151489427	TTTTTGAGACAGGGT[-/CTCC]CTCTGTCATCCAGGC	4703
rs752937326	snp	A/T	3.31587e-05	0.00407164	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151609905	GCGATAATCAATGTC[A/T]GTGACCAAAGTCTGA	4703
rs752947071	snp	C/G	1.73351e-05	0.00294402	intron-variant	NEB, RIF1	GRCh38.p7	2:151494303	GAAAAAGAGTTAACA[C/G]TTACCAAAAAAGGAA	4703
rs752954554	in-del	-/AGCTACTTGGG			intron-variant	NEB	GRCh38.p7	2:151692855	CATGTCTGTAATCCC[-/AGCTACTTGGG]AGGCTGAGGCAGGAG	4703
rs752957835	snp	C/T	3.31406e-05	0.00407053	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151529230	TGTTGACTTTGTAGG[C/T]GTCCTTGGCTGCTTT	4703
rs752961222	snp	C/T	0.000133264	0.00816177	intron-variant	NEB	GRCh38.p7	2:151538096	TGTATATGTATATGG[C/T]GAGTTGTAGAGCCCA	4703
rs752963578	snp	C/T	1.65679e-05	0.00287814	missense, intron-variant	NEB	GRCh38.p7	2:151650702	ACTTCTTGGCCAGTA[C/T]CACTCCCAACATGTC	4703
rs752967926	snp	C/T	1.65712e-05	0.00287843	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151525174	TTACATCACTTTGCT[C/T]CTTGGCCACTTCCAT	4703
rs752975981	in-del	-/TTTTC			intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151507061	TTCAACATTGCTTTG[-/TTTTC]TTTATTTGTCCTATA	4703
rs752982584	snp	C/T	2.26781e-05	0.00336727	intron-variant	NEB, RIF1	GRCh38.p7	2:151512849	TAATCTGTAAAACAA[C/T]ACCGAATAGTTGGGT	4703
rs752983457	in-del	-/AC			intron-variant	NEB, RIF1	GRCh38.p7	2:151494426	TGTAGTTACAGCAAG[-/AC]ACACAACCAGGATAG	4703
rs752988895	snp	A/G	1.82022e-05	0.00301675	intron-variant	NEB	GRCh38.p7	2:151642693	ATTTCTAAAATAGAC[A/G]TTAATAGTAAGTTGG	4703
rs752988954	snp	C/T	1.66432e-05	0.00288467	missense	NEB	GRCh38.p7	2:151553499	GGTCATCCTTGTATA[C/T]AATCTAGAGGGTTTT	4703
rs752989502	snp	A/G	0.000110932	0.00744674	intron-variant	NEB, RIF1	GRCh38.p7	2:151501523	AATCAACCTGGACCC[A/G]TCATTTTTTAGGTAG	4703
rs752994973	snp	A/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151489823	ATGAAAGTTTTCTGA[A/T]ATCATTAATATGAAA	4703
rs752996600	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151557874	GAATGTATCTCAAAA[G/T]AGTAAGAGCTATTTA	4703
rs753000183	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151523479	AACAGATACCTGAGA[A/G]GACAAGGAAAAAGAA	4703
rs753001657	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151705778	CTTTCAAAGCAACTT[A/G]AATGGAGCTGGAGGC	4703
rs753005851	snp	A/G	1.65649e-05	0.00287788	synonymous-codon	NEB	GRCh38.p7	2:151674528	GATGGGAATAGCATC[A/G]CCCAGCACATTGTTG	4703
rs753014048	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151573302	TTGAATATTAGTCTT[A/G]TTCATATAATATCAA	4703
rs753019048	snp	A/G	6.64176e-05	0.00576233	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151529296	ATTTATTTCTTTGGT[A/G]TACTTCTTTGTATTT	4703
rs753027887	snp	A/G	1.65619e-05	0.00287762	missense, intron-variant	NEB	GRCh38.p7	2:151631157	CCTTATTCATGTTGA[A/G]AGCATTGTTCTTGGC	4703
rs753043192	snp	C/T	3.88221e-05	0.00440563	intron-variant	NEB	GRCh38.p7	2:151570424	AAAGCAGATGGGTCA[C/T]AGCATGTCCTCTTGA	4703
rs753048510	in-del	-/TCATAGTCC	1.65656e-05	0.00287794	cds-indel, intron-variant	NEB	GRCh38.p7	2:151610576	GCATCTGCTCTCAGA[-/TCATAGTCC]TCATAGTCCTTCATC	4703
rs753052594	snp	C/T	4.98442e-05	0.00499196	intron-variant	NEB	GRCh38.p7	2:151682638	CAGTCACCACTCTCC[C/T]TCTGACACACCCAGT	4703
rs753061996	snp	A/T	1.65627e-05	0.00287769	missense, intron-variant	NEB	GRCh38.p7	2:151614477	CTTGTACTCCCTGTC[A/T]CTCTGGATCTTGGCC	4703
rs753063012	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151638587	ATTTTCCAGAACGAA[C/T]GGACTGATTTATGAG	4703
rs753064438	snp	A/G	6.63471e-05	0.00575927	missense	NEB	GRCh38.p7	2:151656413	CATCCTCGAGACTGC[A/G]GAAACCAACCATTTT	4703
rs753076994	snp	A/T	5.28797e-05	0.0051417	intron-variant	NEB	GRCh38.p7	2:151690679	CTTACATTTTAAATG[A/T]GCAAAGCACTCTGGG	4703
rs753081037	snp	A/T	4.1855e-05	0.00457447	intron-variant	NEB	GRCh38.p7	2:151547761	GGAGGAAATATCATT[A/T]CAGGCATTTAGTAGG	4703
rs753098235	snp	A/T	9.42951e-05	0.00686576	intron-variant	NEB	GRCh38.p7	2:151567506	AGGAATATAAATTCC[A/T]TCAGTTTTGACAAGC	4703
rs753115433	snp	A/T	1.68439e-05	0.00290201	intron-variant	NEB, RIF1	GRCh38.p7	2:151524640	GGGAAGAAAATGTTT[A/T]CTCAAGAGAGAGGCT	4703
rs753119399	snp	C/T	9.16184e-05	0.00676763	synonymous-codon	NEB	GRCh38.p7	2:151694591	TTTAATGTCAAACTT[C/T]TTGGCTTTGCTCTTC	4703
rs753135135	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151548097	AAGTTTTGCATCATA[A/G]TCTATGGAACCGAGT	4703
rs753145197	snp	A/C	3.3461e-05	0.00409016	intron-variant	NEB	GRCh38.p7	2:151674613	CAAACAGAATGTCAG[A/C]ATCTGTAAGTGATTC	4703
rs753146053	snp	C/G	1.6607e-05	0.00288153	intron-variant	NEB	GRCh38.p7	2:151725576	CTGAAAAGAATATCA[C/G]ATATTAGCCTAACAA	4703
rs753150044	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151526573	TTATTCCGTCTTTAC[A/G]GAGGAGGAAACTGTA	4703
rs753151349	snp	C/T	3.39605e-05	0.00412057	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151502840	TCTCCATCTCTGGAG[C/T]GATAGGTGTTGGGAT	4703
rs753157256	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151513002	AGTTTTATACCAAAG[A/G]GTGAGATTCAGTAAG	4703
rs753157636	snp	A/G	5.03859e-05	0.005019	missense	NEB	GRCh38.p7	2:151727698	AAACTTACTGGGCTA[A/G]AAAGATCCTGCATTT	4703
rs753177210	snp	A/G	2.3646e-05	0.00343838	intron-variant	NEB, RIF1	GRCh38.p7	2:151516566	CTTTGTATTTCACCT[A/G]GTGATAGAAAGCCAT	4703
rs753178123	snp	G/T	8.31732e-05	0.00644823	intron-variant	NEB, RIF1	GRCh38.p7	2:151490336	TCAATGAGCTGGCCG[G/T]GTGGGACTGCCAAAA	4703
rs753180567	snp	C/T	1.68369e-05	0.0029014	missense	NEB	GRCh38.p7	2:151541461	CCTGACTCTGAAGCT[C/T]CTGCCCTCGCTTGGC	4703
rs753192734	in-del	-/CT	1.6593e-05	0.00288031	frameshift-variant, intron-variant	NEB, RIF1	GRCh38.p7	2:151503378	CTTGATTGCGTTTGA[-/CT]CTCTCAATCTCTGGA	4703
rs753198978	snp	A/G	1.65644e-05	0.00287783	missense, intron-variant	NEB	GRCh38.p7	2:151627081	AATTTCAGCTTGTCC[A/G]GAGGCTGGCGGTAGA	4703
rs753227351	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151684171	TATACTTAACACCAC[C/T]GAACTGTACACTTGA	4703
rs753227895	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151673553	CCTCCGAGGAAGATG[C/T]TTTCAGTATCATTCC	4703
rs753229810	snp	C/T			missense	NEB	GRCh38.p7	2:151553896	GGTGGCAAATCCATT[C/T]GTGGAGGCGCAGGCG	4703
rs753231552	snp	A/T	3.38513e-05	0.00411394	intron-variant	NEB	GRCh38.p7	2:151666405	CTTATATTTGCACTA[A/T]TTGAAAACAAAGGGC	4703
rs753234017	snp	G/T	1.65905e-05	0.0028801	missense	NEB	GRCh38.p7	2:151541527	AGATTGACTTCTGCT[G/T]CTTGCCTGCAGCTCT	4703
rs753238617	snp	A/G			upstream-variant-2KB	NEB	GRCh38.p7	2:151735066	TACTAAACCAAGAGG[A/G]TATACCAAAATCCTA	4703
rs753240480	snp	C/G			missense, intron-variant	NEB	GRCh38.p7	2:151627023	CATATTGAGAGCATT[C/G]TTCTTGGCCAGCACC	4703
rs753243290	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151500800	GATGGAATTTCACCA[C/T]GTTGGCTAGGCTGGT	4703
rs753245497	snp	C/G	1.67077e-05	0.00289026	intron-variant	NEB	GRCh38.p7	2:151656040	TATAAAGAAGATAAG[C/G]AAATTCTACTTTATC	4703
rs753245846	snp	C/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151523877	GGGCAGTTAATATAT[C/G]TATGTTTAATGAAAA	4703
rs753251668	snp	C/T	1.84599e-05	0.00303803	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151527510	GGGATGACTTGGCAG[C/T]CTGGAGGAAGTCCGG	4703
rs753253128	snp	A/G	3.31774e-05	0.00407279	synonymous-codon	NEB	GRCh38.p7	2:151548311	GCATTCAGGTACCTC[A/G]CTGGTAACATTGTTG	4703
rs753256008	snp	C/T	1.65644e-05	0.00287783	missense, intron-variant	NEB	GRCh38.p7	2:151629586	CCACGATGGGGATGG[C/T]GTCACTTCGCAAGTC	4703
rs753256671	snp	C/T	3.34734e-05	0.00409091	missense, intron-variant	NEB	GRCh38.p7	2:151650863	TGGCCAAGTTGCTTT[C/T]GGTAGCCTTGTTTGT	4703
rs753257736	snp	C/G	5.5004e-05	0.00524395	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151493840	AGGGTGTGGGGGTTG[C/G]TTTCCCCAGGTTCTC	4703
rs753261774	snp	A/C	1.6563e-05	0.00287771	missense	NEB	GRCh38.p7	2:151563643	TCCAGACAGTGAACC[A/C]CACCAGGGAATTCAC	4703
rs753267809	snp	A/G	4.9675e-05	0.00498348	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151643914	CTTGTAGTCCACGTC[A/G]CTGACTAAGGTCTGG	4703
rs753284331	snp	C/G			missense	NEB	GRCh38.p7	2:151725480	ATCTTGTACTTTTTT[C/G]ATTCTGCGAAGTTCT	4703
rs753291174	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151544648	CAAATTGGCTCAATG[G/T]TGCATTTGCAAAAGC	4703
rs753291655	snp	A/G	1.69634e-05	0.00291229	intron-variant	NEB	GRCh38.p7	2:151672689	ATTTATACTGTGGAG[A/G]CAGAATTGGGTTAGC	4703
rs753301409	snp	C/G/T	6.1004e-05	0.00552259	intron-variant	NEB	GRCh38.p7	2:151664908	TACAGCAGGACAAGT[C/G/T]TGACCCAATGCTAGC	4703
rs753302781	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151671699	TTGATTCCACTGAAG[A/C]CTTCAAAACTAAATT	4703
rs753302955	snp	C/T	1.95578e-05	0.00312706	intron-variant	NEB	GRCh38.p7	2:151692442	TTCATGTCTTTGCTG[C/T]ACTTTAACTGAAGGG	4703
rs753319208	snp	A/G	3.35739e-05	0.00409705	intron-variant	NEB	GRCh38.p7	2:151670992	CGTGTGGTTATTTAC[A/G]GGCAAATCATTTTGA	4703
rs753322285	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151674838	CCAGAGAAAAACAAA[C/T]AAAGGTTCTGGAAAC	4703
rs753328294	snp	A/G	1.65614e-05	0.00287757	synonymous-codon	NEB	GRCh38.p7	2:151671068	CAACACCATGCCCAT[A/G]GAATCAGGCACACTT	4703
rs753329732	snp	A/T	3.56094e-05	0.00421941	intron-variant	NEB	GRCh38.p7	2:151724839	TGAGTACCCCAGCCA[A/T]CCATATCATTGCCTT	4703
rs753335163	snp	A/G	2.37386e-05	0.0034451	synonymous-codon	NEB	GRCh38.p7	2:151565806	GAGCCACTCCAGGTC[A/G]GCTCTGTAGACATTC	4703
rs753340681	in-del	-/AC	1.65754e-05	0.00287879	frameshift-variant	NEB	GRCh38.p7	2:151723480	CCCAGTCTTCAGTGT[-/AC]AGTTTCTAAATCAAA	4703
rs753361326	snp	C/T	1.65625e-05	0.00287766	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151524375	CCGAGCATGCTTAAG[C/T]CATGGCTGCCTTCCT	4703
rs753363321	snp	A/T	1.73228e-05	0.00294297	missense, intron-variant	NEB	GRCh38.p7	2:151636237	CTCACGTCACTGATG[A/T]TGTCCCTGGAGGCCT	4703
rs753372799	snp	A/G	1.72674e-05	0.00293827	intron-variant	NEB, RIF1	GRCh38.p7	2:151492369	CAGCCAGCCAATCCT[A/G]AAGAATTCCTGACTC	4703
rs753378097	snp	C/T	9.85309e-05	0.00701824	missense	NEB	GRCh38.p7	2:151678183	TAGTCTTTTTTGTAC[C/T]GAACCTATTGTAAAC	4703
rs753378567	snp	A/G	1.66927e-05	0.00288895	intron-variant	NEB, RIF1	GRCh38.p7	2:151485955	GTGGGGATGGAAAAG[A/G]GGAAATATTATATGT	4703
rs753381922	snp	C/G	1.65693e-05	0.00287826	missense	NEB	GRCh38.p7	2:151672624	GGGATCATCCTGGAG[C/G]CTTCTGAAACCCACA	4703
rs753382223	snp	C/G	3.32895e-05	0.00407966	missense, intron-variant, utr-variant-3-prime	NEB, RIF1	GRCh38.p7	2:151497657	TGATTGTGTTTGACT[C/G]TTTCCATCTCGGGAG	4703
rs753384215	snp	C/T	0.000157604	0.00887566	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151508030	TTCTTTTGGTTCTCC[C/T]GGACTCTCTGTATCT	4703
rs753394142	snp	A/T	0.000123191	0.0078473	intron-variant	NEB	GRCh38.p7	2:151687748	TCTGGACAAGAAAAA[A/T]TCAGCAAAGGAATGA	4703
rs753405799	snp	A/G	1.70464e-05	0.0029194	intron-variant	NEB, RIF1	GRCh38.p7	2:151527055	CAGAAGAAAAGGGAA[A/G]GGTGACAGCACAGGA	4703
rs753408606	snp	A/G	1.65855e-05	0.00287967	intron-variant	NEB	GRCh38.p7	2:151619409	CACAGACACGTTTCA[A/G]ATCCGCTTTTAACAT	4703
rs753409626	snp	C/T	8.77385e-05	0.00662281	missense	NEB	GRCh38.p7	2:151547464	CATAGCGGCAATGGA[C/T]CACTTGGGGTGTGTA	4703
rs753417634	snp	A/G	1.6937e-05	0.00291002	synonymous-codon	NEB	GRCh38.p7	2:151540428	GTCTTTCATCTTTTC[A/G]TATTGAATCTTGTAC	4703
rs753417927	in-del	-/T	7.05443e-05	0.00593862	intron-variant	NEB	GRCh38.p7	2:151562816	AGTTCAACTAATATG[-/T]TTTTAAAGACAAAAA	4703
rs753425308	snp	C/T	8.01635e-05	0.00633051	intron-variant	NEB	GRCh38.p7	2:151707033	GATAAAGTAACTCTA[C/T]GGGTTATTTTTGCCC	4703
rs753426448	in-del	-/TT	5.41169e-05	0.00520149	intron-variant	NEB	GRCh38.p7	2:151733102	AGTTTGCTGTCAGTG[-/TT]TTTTTTTTAAATCTT	4703
rs753428817	snp	C/T	5.91465e-05	0.00543781	missense	NEB	GRCh38.p7	2:151684930	GCATATCAAGAGGTG[C/T]CGTGTAGATAGTTTT	4703
rs753430815	snp	A/G	1.65941e-05	0.00288041	intron-variant	NEB	GRCh38.p7	2:151552808	AACAAGCCCATGTTG[A/G]ACCATTCCTTATGCT	4703
rs753443619	snp	C/T	2.13915e-05	0.00327037	missense	NEB	GRCh38.p7	2:151562690	CACTGGTGGAAATAG[C/T]GTCGATACTCCAGGT	4703
rs753450456	snp	C/T	8.31083e-05	0.00644571	missense, intron-variant	NEB	GRCh38.p7	2:151612320	CTCTCTTCACTTTCT[C/T]GACCTCTACAGAGCC	4703
rs753467772	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151658233	GTGGCTGAATGTTCT[C/T]ACAAGTAACATAACT	4703
rs753473309	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151724593	TCCTCAGCTTCTTTG[A/G]TGACACTGGGACTTC	4703
rs753477337	snp	A/G	3.35644e-05	0.00409647	intron-variant	NEB	GRCh38.p7	2:151629674	AGGCAAAGAGTTAAA[A/G]CAAAAGGTTTGACAT	4703
rs753482224	snp	A/G			intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151498750	TATTTGGGTTTTACA[A/G]ACATTGTGTATATGG	4703
rs753484461	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151558023	GTTCTGGCCAGGGCA[A/G]TGAGGCAAGAGAAAG	4703
rs753488259	snp	A/G	2.00753e-05	0.00316816	intron-variant	NEB	GRCh38.p7	2:151650535	ACTCATATAAAATAT[A/G]AATTAATATATAAAC	4703
rs753488581	snp	C/T	1.66258e-05	0.00288316	missense, intron-variant	NEB	GRCh38.p7	2:151643319	GTCATCCAGCCAATG[C/T]CTTTTAGCCACTGAA	4703
rs753492033	snp	C/T	1.69743e-05	0.00291322	missense	NEB	GRCh38.p7	2:151688293	GCTTTGGTACTTACA[C/T]CACTCAGATTATAGG	4703
rs753494666	snp	A/G	1.68655e-05	0.00290387	synonymous-codon	NEB	GRCh38.p7	2:151567210	TGCCTGAATAACATC[A/G]TTCTGGTCAGGATGA	4703
rs753497414	snp	C/T	1.65603e-05	0.00287747	missense	NEB	GRCh38.p7	2:151664535	GAGGCTCTTGCAGCC[C/T]TTATTGCAATGGCAT	4703
rs753498671	snp	A/G	1.65767e-05	0.00287891	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151650319	TCTTTTCTGCCTCTA[A/G]AGAACCCAAGGGACT	4703
rs753503996	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151672036	ATAGAAAATTCTTCT[A/G]TTTTTGCATTTTGTA	4703
rs753510989	snp	A/C	3.06753e-05	0.00391621	missense	NEB	GRCh38.p7	2:151706911	TCCTGCTGCCTTCAG[A/C]TGCCTAAGCTGTGGG	4703
rs753516486	snp	A/G	1.65608e-05	0.00287752	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151514360	TGCTCTTAGCATGTC[A/G]GGTGTATCTTCCATT	4703
rs753520710	snp	A/G	1.65627e-05	0.00287769	intron-variant	NEB, RIF1	GRCh38.p7	2:151524485	GGCAATGGCTGTTGG[A/G]GACTGGGGACATTTT	4703
rs753521859	snp	C/T	1.82128e-05	0.00301762	intron-variant	NEB	GRCh38.p7	2:151710569	AGAAAATAAGACAAG[C/T]ATAACTCATGAATTG	4703
rs753525909	snp	C/T	3.04233e-05	0.0039001	intron-variant	NEB	GRCh38.p7	2:151664717	TAAGTATCAGTTCCC[C/T]TTAACCTTCTCCCCA	4703
rs753537388	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151617171	AATTCCTGATAACCT[A/G]TTAATAAAATGGTAG	4703
rs753546355	snp	C/T	1.66021e-05	0.0028811	intron-variant	NEB	GRCh38.p7	2:151692021	ATGGCTCTCAAACAA[C/T]GTCACTGTGAGGCAT	4703
rs753550094	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151689265	GCTGGAGTACAGTGA[A/C]ACAATCTCGGCTCAC	4703
rs753552984	snp	A/C	1.66649e-05	0.00288655	missense	NEB	GRCh38.p7	2:151724936	CATATAGTCTTAGCA[A/C]CATCACCATCCATTC	4703
rs753559022	snp	C/T	1.65943e-05	0.00288043	intron-variant	NEB	GRCh38.p7	2:151626965	ATCTTGAATGACATA[C/T]AGCCCTGTCTTATTT	4703
rs753569565	snp	C/T	0.000304368	0.0123325	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151607606	GGCTTCCTGATACAG[C/T]TTCTGTGGAGAGGAG	4703
rs753570540	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151499996	TCATTAAGGTTTCAA[A/G]TAGATACAAATAATA	4703
rs753570764	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151560240	TGGTTTATTTTTGCC[C/G]TACATCCATGTAATT	4703
rs753573270	in-del	-/ATT	7.88426e-05	0.00627814	intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151497080	CATGAGTAACATTTC[-/ATT]ATTTGTTGAAAGGTT	4703
rs753574965	snp	A/G	1.70409e-05	0.00291893	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151617370	TTTACTTACATCACT[A/G]TAGTTTATTCGGTTG	4703
rs753576597	in-del	-/CCAAAAAG			intron-variant	NEB, RIF1	GRCh38.p7	2:151494273	GGGAATCCAATGGGT[-/CCAAAAAG]CCAAAAAGAAAAAGA	4703
rs753577039	snp	A/G	3.31225e-05	0.00406941	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151526023	CTGGTAGTGTTGTGT[A/G]TGAGCCCTGTGCCAA	4703
rs753586000	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151625985	TCTGTAGTATGACTA[G/T]ATTAACAAATCCTTC	4703
rs753592387	snp	A/G	1.98057e-05	0.00314682	intron-variant	NEB	GRCh38.p7	2:151680061	ACAAACAAATAAAGT[A/G]GAAAGAAAATTTAAT	4703
rs753594856	snp	G/T	1.66527e-05	0.00288549	missense	NEB	GRCh38.p7	2:151667856	ATTGGGATGGCATCT[G/T]GTCTCAAATCATAGC	4703
rs753609843	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151692717	GCTCACACCTGTCAT[C/T]ACAGCACTTTGGGAA	4703
rs753611103	snp	C/T	1.65647e-05	0.00287786	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151505488	ACTACCGAGCTAATG[C/T]GCTTCTGCGTCTCCT	4703
rs753618186	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151532362	TTGTTTTACTCATAA[C/T]ATATTGTATTGAACA	4703
rs753638647	snp	C/G/T	6.26945e-05	0.00559857	missense	NEB	GRCh38.p7	2:151709706	TATACTCTGGTGTTT[C/G/T]GGTCTGCATGAAGTA	4703
rs753647278	snp	C/T	8.28878e-05	0.00643716	missense, intron-variant	NEB	GRCh38.p7	2:151644565	TCCTCATAACCCATT[C/T]GGTAGAGTTTCTGTT	4703
rs753652055	snp	A/G	1.81585e-05	0.00301313	intron-variant	NEB	GRCh38.p7	2:151551700	AGAGGCTGATGGAAC[A/G]GATTTCTGCTGGGCA	4703
rs753653230	snp	A/G	3.31675e-05	0.00407218	synonymous-codon	NEB	GRCh38.p7	2:151568331	CTGGTCCAGTATCCT[A/G]GCAGCCTCCTGGGCA	4703
rs753658752	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151661031	GTGGTGACTAGTTAT[C/G]AGAATCCCTGTTCTA	4703
rs753669326	snp	A/C/T	1.76266e-05	0.00296867	missense, intron-variant	NEB	GRCh38.p7	2:151625581	ACATGATTTCAGGTG[A/C/T]ATCAGGCATAATATG	4703
rs753673376	snp	C/T	1.65938e-05	0.00288039	missense	NEB	GRCh38.p7	2:151540717	TGACCATGTCCTTCA[C/T]GTCTTTAGCATGCTT	4703
rs753676768	in-del	-/TTT			intron-variant	NEB, RIF1	GRCh38.p7	2:151493286	AATGAGAAAGGCGTG[-/TTT]TTTTTATGATGTTAA	4703
rs753681154	snp	A/G	1.95881e-05	0.00312948	missense	NEB	GRCh38.p7	2:151576152	AAAAACTAACTCACA[A/G]TACTAATATTTTCAG	4703
rs753681247	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151611263	GCTGTGTGATCTTGA[A/G]AAAGGTACATAACTC	4703
rs753682489	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151631578	GGAGTGATCCCAAGT[A/T]ATATCTTCTGTCAGT	4703
rs753686179	snp	A/T	1.66521e-05	0.00288544	missense, intron-variant	NEB	GRCh38.p7	2:151643825	AGACTCACATCGCTC[A/T]GGAGGTCATAGGCCT	4703
rs753691207	snp	A/G/T	3.31248e-05	0.00406958	missense	NEB	GRCh38.p7	2:151680785	ATTGGAGCATCTTCA[A/G/T]TCGAGGTAAACTTGA	4703
rs753692124	snp	A/G	6.84486e-05	0.00584975	intron-variant	NEB	GRCh38.p7	2:151695703	ACAGAGAGAGAACCA[A/G]TTAGTTCAGAAGAAT	4703
rs753692957	in-del	-/CC			intron-variant	NEB, RIF1	GRCh38.p7	2:151495569	CCTGCAAACCTCAAT[-/CC]CTAGGTAATTTACAA	4703
rs753696014	snp	A/G	1.65888e-05	0.00287996	missense	NEB	GRCh38.p7	2:151677599	TTCTGTTTTGCCTGG[A/G]CCATAACTGGGGAGT	4703
rs753714285	snp	A/G	1.78899e-05	0.00299076	missense, intron-variant	NEB	GRCh38.p7	2:151609828	CTCTGCAGGTCATAG[A/G]CCTTTTTTGCTTGGA	4703
rs753718572	snp	C/G/T	3.31242e-05	0.00406955	missense, synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151640028	CACCCAGCCAATGCC[C/G/T]CTCATCCACTGGAGA	4703
rs753725565	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151716471	GATCATGTATTTATG[C/T]ACAGTTCTAAAGTTA	4703
rs753739208	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151645550	ACCAGATTATTTAAA[A/G]TGCCTATTGATCTTG	4703
rs753746154	snp	C/T	1.68624e-05	0.0029036	intron-variant	NEB	GRCh38.p7	2:151640336	ACCTCTGCACGTTAT[C/T]ATGACTCTCAGTACT	4703
rs753749364	snp	A/C	1.65789e-05	0.0028791	intron-variant	NEB, RIF1	GRCh38.p7	2:151526121	CTGGGGCGTTCTCCC[A/C]AGAGGGAAGCAGAAC	4703
rs753750022	snp	C/T	3.3157e-05	0.00407154	intron-variant	NEB, RIF1	GRCh38.p7	2:151505605	AAAAGAAAGGTATTA[C/T]TACATGCTGGACTGT	4703
rs753752286	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151552451	CACAAAGTTACTTCA[C/T]AGACTCGCATCACCT	4703
rs753752389	snp	C/T	1.65663e-05	0.002878	intron-variant	NEB, RIF1	GRCh38.p7	2:151514474	ACAAGAAAGCCCAGA[C/T]TGATTCTCTCAGGCA	4703
rs753761094	snp	A/G	1.65649e-05	0.00287788	missense	NEB	GRCh38.p7	2:151692091	CAACTTTCATGCAGT[A/G]TGTGTGATATGGGTC	4703
rs753769042	snp	G/T	0.000111582	0.00746851	intron-variant	NEB	GRCh38.p7	2:151546033	ACAGAAATACAAGTT[G/T]ATTAATCATTTAAGG	4703
rs753799779	snp	C/T	1.74689e-05	0.00295536	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151502859	AGGTGTTGGGATTCC[C/T]TTCCCCAAATTTTCT	4703
rs753810451	snp	G/T	1.73718e-05	0.00294714	missense	NEB	GRCh38.p7	2:151655331	GTATCAGGCATCACA[G/T]GAATCTTGGTCTTAT	4703
rs753812451	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151678909	TTATTCAATCATCAC[A/G]TATTTACACTGGTGC	4703
rs753821338	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151633352	CAGTAATTTCTTTTT[A/C]AAGTAAAAACGTTTC	4703
rs753826855	snp	A/G	1.74306e-05	0.00295211	intron-variant	NEB	GRCh38.p7	2:151655228	TTTATAAGTTCATAA[A/G]TTTCAATACAAAACT	4703
rs753828020	snp	C/T	3.53838e-05	0.00420603	utr-variant-3-prime, intron-variant	NEB, RIF1	GRCh38.p7	2:151485710	TCTAAACCGAAACAT[C/T]GACTGCAGGATCTGT	4703
rs753828954	snp	A/G			missense	NEB	GRCh38.p7	2:151659135	ATGATGTGGACTTTG[A/G]TTTTGTCAGCCTCCC	4703
rs753830499	snp	C/T	1.77862e-05	0.00298207	missense	NEB	GRCh38.p7	2:151553829	AGTCACAGGCTTACA[C/T]CGCTGATCTGATCTG	4703
rs753834454	in-del	-/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151488818	TAAATAACTTACCCC[-/T]TTTCTTGCTGATTTA	4703
rs753852194	in-del	-/A	4.97451e-05	0.00498699	intron-variant	NEB	GRCh38.p7	2:151659043	GGAGAGAAAGATGAC[-/A]AACAGGGGGAACTAT	4703
rs753852471	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151729752	TGACTGCACTAGCTC[A/G]GTTGATTTGGAATGT	4703
rs753854812	in-del	-/AG	2.69771e-05	0.00367258	frameshift-variant	NEB	GRCh38.p7	2:151547484	TGGGGTGTGTATGGC[-/AG]AGAGATCATGTGGCC	4703
rs753855949	snp	C/G	4.88938e-05	0.00494414	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151513648	TGGCCATGGCATTCA[C/G]GCCTCTTCCTTTGAC	4703
rs753863257	snp	C/G	3.31741e-05	0.00407259	missense, intron-variant	NEB	GRCh38.p7	2:151619700	TATCTTGGGGTCATC[C/G]TGTACTGCTCGGGCG	4703
rs753864118	snp	C/T	0.000281692	0.0118645	synonymous-codon	NEB	GRCh38.p7	2:151656357	GTACTCCCGATCAGA[C/T]TGCATCTTAGCCACT	4703
rs753865894	snp	G/T	1.66109e-05	0.00288187	missense	NEB	GRCh38.p7	2:151663699	AGCATGTCCACCGGG[G/T]TGTGGAAGGAGGTCT	4703
rs753872949	snp	G/T	4.26776e-05	0.0046192	missense	NEB	GRCh38.p7	2:151549715	TATCCAGTGGGCAGG[G/T]TGCGCAGGCTGGTTT	4703
rs753885527	in-del	-/A			intron-variant	NEB	GRCh38.p7	2:151681135	CTAAGCAGAATCTGG[-/A]AACATCACAGAGTTT	4703
rs753885744	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151564430	AGTGCTGGGATTATA[A/G]GCGTGAGCCACCATG	4703
rs753886676	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151680318	TACACCAACCACCTA[C/T]ATTATATTTTGTGGG	4703
rs753896636	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151538907	TATTTTCAACGTCAA[A/T]CAGTTCTTTTCTTTT	4703
rs753909079	snp	A/G	2.05586e-05	0.00320607	intron-variant	NEB	GRCh38.p7	2:151570455	TGCACCTAGGGCATC[A/G]GCTGAAAAAAAAAAA	4703
rs753909381	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151717697	TCCTCCTCAAGACTC[A/G]TGGCCCTAGATCTGC	4703
rs753909783	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151718636	CCTTCAGAGGGAATG[A/G]CTCCTGCACCCAGGG	4703
rs753917990	snp	C/T	3.31356e-05	0.00407022	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151492208	ATGTTCTTCTTTACT[C/T]GTTCAGTGATAGGAT	4703
rs753920981	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151612508	TGTGTAAATTTCTGG[A/G]AAGACCCACAGGATT	4703
rs753924668	snp	A/T	1.72015e-05	0.00293265	intron-variant	NEB, RIF1	GRCh38.p7	2:151529333	TGGGAGGAAACACAG[A/T]GACAAGATTAATTTT	4703
rs753936212	snp	C/G	1.83112e-05	0.00302576	intron-variant	NEB	GRCh38.p7	2:151619802	AGAAGGAAGCACAAA[C/G]GGCTATTCCCTGTTG	4703
rs753943333	snp	A/G	0.000101693	0.00712995	intron-variant	NEB	GRCh38.p7	2:151674633	GTAAGTGATTCCTCA[A/G]CTGCTGGGATTGTTT	4703
rs753947526	snp	C/G/T	3.43384e-05	0.00414346	synonymous-codon, missense, intron-variant	NEB	GRCh38.p7	2:151639887	GGCATTATTTTTGGC[C/G/T]AACACTTGTTCCAGA	4703
rs753949296	snp	A/G			missense, intron-variant	NEB	GRCh38.p7	2:151620956	GCCTTGGCAGCCACA[A/G]TGGGAATGGCATCAC	4703
rs753957097	snp	G/T	1.6566e-05	0.00287797	missense	NEB	GRCh38.p7	2:151679819	CTTTCAAGTCTGCTT[G/T]GTACATATTCTGAAA	4703
rs753965951	snp	C/T	1.65792e-05	0.00287912	synonymous-codon	NEB	GRCh38.p7	2:151690787	AGAATCAGTGACTGC[C/T]GTGAATTTGGTCTTA	4703
rs753968560	snp	A/T	9.20429e-05	0.00678329	missense, intron-variant	NEB	GRCh38.p7	2:151592101	GCTGGCACGTTCACA[A/T]TAGCCTTCTCTTTCT	4703
rs753969729	snp	A/C/T	3.43343e-05	0.00414321	missense	NEB	GRCh38.p7	2:151568133	CATCTGGAGGCAAAA[A/C/T]GTAACCTGTGGCTTT	4703
rs753972462	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151609444	ATTCCATAATATAAT[C/T]ATTTGATATTTCAAA	4703
rs753976426	in-del	-/AAGCTGAAAAA	1.66183e-05	0.00288251	intron-variant	NEB, RIF1	GRCh38.p7	2:151490075	TTTTTGCATGTTTGT[-/AAGCTGAAAAA]AAGGGGGCAAATTCT	4703
rs753978077	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151654752	TTAGGGATGAGGAAA[A/G]TGAGACTTAGATAGG	4703
rs753983177	snp	C/T	4.89416e-05	0.00494656	intron-variant	NEB, RIF1	GRCh38.p7	2:151512859	AACAACACCGAATAG[C/T]TGGGTAAATGTTTGC	4703
rs753985158	snp	A/C	1.6703e-05	0.00288985	intron-variant	NEB, RIF1	GRCh38.p7	2:151519773	CGGTATTTAACCTAA[A/C]AGCAAATGCAAACAT	4703
rs753987329	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151540141	TCAGGAGAGAATTGA[A/G]AAGAATAGGCTTCTG	4703
rs753992038	snp	A/G	3.31697e-05	0.00407231	missense	NEB	GRCh38.p7	2:151548315	TCAGGTACCTCGCTG[A/G]TAACATTGTTGACTC	4703
rs753993227	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151668333	CTAAAAATCCAGATG[C/T]AGTACAACTCAGCTT	4703
rs753996512	snp	C/T	2.53649e-05	0.00356116	missense, intron-variant	NEB	GRCh38.p7	2:151642868	GCTTCTGTATAGAGG[C/T]GCTAAGAGAAACAGA	4703
rs753997031	snp	C/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151520063	AAAAAAATGGAAAAG[C/G]CTTCAGGCTAAATTC	4703
rs754001835	snp	A/C	1.65616e-05	0.00287759	missense, intron-variant	NEB	GRCh38.p7	2:151631174	GCATTGTTCTTGGCC[A/C]GCACCTGCTCTAGAG	4703
rs754008028	snp	A/G	1.66272e-05	0.00288328	missense	NEB	GRCh38.p7	2:151727728	TTCTGACTGTGTGCA[A/G]TGTAGGGGGTCATGA	4703
rs754046288	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151574425	ACTGAGGATGAGTTG[A/G]CCTTTGATTTGAGAT	4703
rs754047069	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151687017	CTAAAGTCAATGAAG[A/G]ACGATACTCTATTAA	4703
rs754048535	in-del	-/C			intron-variant	NEB, RIF1	GRCh38.p7	2:151513836	TTCACCTTCGCTCTT[-/C]CGTGTGGTAGGATGA	4703
rs754048990	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151706644	CAGGTGCCCAGAGCT[A/C]CTAAGCAAGTGAGAA	4703
rs754061484	snp	G/T	3.32574e-05	0.00407769	intron-variant	NEB	GRCh38.p7	2:151725592	ATATTAGCCTAACAA[G/T]ACAGCAGTGAAAATT	4703
rs754061952	snp	A/G	8.28411e-05	0.00643535	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151525188	TTCTTGGCCACTTCC[A/G]TAGCATGTTTCACCT	4703
rs754065526	snp	C/T	1.67885e-05	0.00289724	missense	NEB	GRCh38.p7	2:151656443	TCCCCTTCCCTTTTT[C/T]ATAATTGTACTTGTA	4703
rs754071232	snp	A/G	1.65471e-05	0.00287633	intron-variant	NEB	GRCh38.p7	2:151695563	ATCACATGGTACAGG[A/G]CATAAGGAACTTACA	4703
rs754079017	snp	C/T	3.34493e-05	0.00408944	missense, intron-variant	NEB	GRCh38.p7	2:151614586	CCTTCCTTGTACTTG[C/T]ACTAAAAAAATAGAG	4703
rs754081456	snp	C/T	1.89939e-05	0.00308165	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151531077	CTCTGGGTTTGGCCT[C/T]GTTGTATTCCAATTT	4703
rs754082609	snp	G/T	1.65616e-05	0.00287759	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151518337	CTCTGTAATTCTGTG[G/T]CCTCTTTTAGGTGAA	4703
rs754082773	snp	A/G	1.70391e-05	0.00291878	intron-variant	NEB	GRCh38.p7	2:151576404	TGTTTTGTTGTGTAT[A/G]TGTGTGGTAAAATAA	4703
rs754114947	snp	A/C	1.6715e-05	0.00289089	intron-variant	NEB, RIF1	GRCh38.p7	2:151503335	AGTTTCTTATATGAT[A/C]TATTTGTAAATACCG	4703
rs754118814	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151639389	GTGTATAAACGCTAT[A/C]AAAAAAAATACACAA	4703
rs754120353	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151656517	CTTTGACTAAAAATC[A/G]ATCTAGTGTCAATAT	4703
rs754131951	in-del	-/A			intron-variant	NEB	GRCh38.p7	2:151578096	GAACTCATTCATTAT[-/A]AAAAAAGTACCTCTG	4703
rs754134059	snp	A/T	1.66233e-05	0.00288295	intron-variant	NEB	GRCh38.p7	2:151563775	TAACCAGCCCCTTGA[A/T]CCCCAGTAAAGACTC	4703
rs754134514	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151560009	TTAGAGGTCATAAGA[C/T]TTAAAGGCATAAAGA	4703
rs754136793	snp	A/G	0.000255979	0.0113103	intron-variant	NEB	GRCh38.p7	2:151688421	AAAGGATATTTGAAC[A/G]GTTCAGGGGAACTTC	4703
rs754138745	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151489572	TGGCTAATTTTTTGG[C/T]TTTTAGTAGAGATGA	4703
rs754142587	snp	A/G	1.6585e-05	0.00287962	intron-variant	NEB	GRCh38.p7	2:151643137	AACCTCCTCAAACAA[A/G]CATAGGACTTACATG	4703
rs754144094	snp	A/T	6.08921e-05	0.00551746	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151494179	GCTAATGTTTTCTTG[A/T]TTGCGTTTGACTCTC	4703
rs754156824	snp	C/T	1.67489e-05	0.00289381	intron-variant	NEB	GRCh38.p7	2:151670995	GTGGTTATTTACGGG[C/T]AAATCATTTTGAAAG	4703
rs754158432	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151628305	CACCCACACTCCTTC[A/C]CAAATCCAGCTCTGC	4703
rs754168438	snp	C/G	2.18248e-05	0.00330332	intron-variant	NEB	GRCh38.p7	2:151682782	AACCTAAAACACCAA[C/G]AGAAAGGTTACATTT	4703
rs754177595	snp	A/T	1.65789e-05	0.0028791	missense, intron-variant	NEB	GRCh38.p7	2:151627189	CTCAGCCACTGGAGA[A/T]CAGATTTGTAAATGT	4703
rs754183918	snp	C/G	1.70281e-05	0.00291783	intron-variant	NEB	GRCh38.p7	2:151717404	GGCAATGTCCCAGCT[C/G]TATTTACTTACCTTG	4703
rs754184037	in-del	-/T	1.69957e-05	0.00291506	intron-variant	NEB	GRCh38.p7	2:151627883	GAATAGAAAGGCTTA[-/T]GAAGCCTCATTAATT	4703
rs754196398	snp	G/T			upstream-variant-2KB	NEB	GRCh38.p7	2:151734698	CAATTTTAGGTTGAA[G/T]TTCCCATTTACTGAG	4703
rs754203319	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151502145	AACATTGTATGTTCT[C/T]ACTGATATGTGGGAA	4703
rs754204181	in-del	-/A			intron-variant	NEB, RIF1	GRCh38.p7	2:151513712	TAGTAGCATTAAAAG[-/A]AAAAAAAAAGGTACC	4703
rs754208298	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151657761	AAGTTTATCTAGATC[C/T]CATGAGTCAGGGAGC	4703
rs754212836	snp	A/G	3.31587e-05	0.00407164	intron-variant	NEB	GRCh38.p7	2:151697255	CTTTGTAGTTTTTCT[A/G]TGAGGAGAAGAAATT	4703
rs754215694	snp	C/G	1.88938e-05	0.00307352	intron-variant	NEB, RIF1	GRCh38.p7	2:151525319	AGAGGAAGCTGGGAA[C/G]AGAGTTGGTTTACTT	4703
rs754222404	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151560982	TGGCTCATATATAAG[A/G]GGGAAAAAAAACTCA	4703
rs754222791	snp	C/G	3.31603e-05	0.00407174	missense	NEB	GRCh38.p7	2:151548382	GTGTATACCCATATG[C/G]CTTGGTGTGTTCATA	4703
rs754232689	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151696523	ATACTGTTTAAACTT[A/G]CTAATACTTACTTAG	4703
rs754233089	snp	A/G	1.65932e-05	0.00288034	synonymous-codon	NEB	GRCh38.p7	2:151541537	CTGCTTCTTGCCTGC[A/G]GCTCTGTAGACCAGC	4703
rs754234740	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151732092	TTTGGCACTGCCACC[C/T]AAAATTTGGTTCTGG	4703
rs754243460	snp	C/T	4.96586e-05	0.00498265	intron-variant	NEB	GRCh38.p7	2:151691845	GCTCAATTTCAATAA[C/T]TCAGGGCAGCTAACT	4703
rs754252102	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151675134	TTGAAAAGGCCAACT[A/G]AAGAGGTAAAGAACC	4703
rs754262594	snp	A/C	1.65696e-05	0.00287828	intron-variant	NEB	GRCh38.p7	2:151697324	AAATGTTATTTGGAA[A/C]GTCAAACAATTGTCT	4703
rs754263826	snp	G/T	1.65625e-05	0.00287766	missense, intron-variant	NEB	GRCh38.p7	2:151631226	TCAGCTTGTCCGGAG[G/T]CTGGCGGTAGATGTT	4703
rs754270019	snp	A/G	1.85269e-05	0.00304354	intron-variant	NEB	GRCh38.p7	2:151710579	ACAAGCATAACTCAT[A/G]AATTGACAAATAAGA	4703
rs754272319	snp	A/G	1.70449e-05	0.00291928	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151653995	ACTAGTACTCACATC[A/G]CTAGCAATGTCTCTT	4703
rs754272530	snp	C/G	5.95646e-05	0.00545699	stop-gained, intron-variant	NEB, RIF1	GRCh38.p7	2:151493859	CCCCAGGTTCTCTTT[C/G]TATAACACCTGTGAG	4703
rs754277002	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151676022	ATTAGAAATATATTA[C/T]TTAGTTCCTAAAACT	4703
rs754277025	snp	A/T	1.65965e-05	0.00288062	missense	NEB	GRCh38.p7	2:151662316	ATGCCCTTCATGAAG[A/T]CAGCATAGTCAGCCT	4703
rs754279354	snp	C/T	1.65622e-05	0.00287764	missense	NEB	GRCh38.p7	2:151671090	GGCACACTTGTGAAC[C/T]TGACGGTATCTGGGT	4703
rs754285878	snp	A/G			utr-variant-5-prime	NEB	GRCh38.p7	2:151733779	TTTTCTTTCGTTTCT[A/G]TAGCTCTCGTTCAAA	4703
rs754290375	in-del	-/G	1.80699e-05	0.00300577	intron-variant	NEB, RIF1	GRCh38.p7	2:151519080	TAACCTGTGTGTTAT[-/G]GGGGGAAGAAAGGAA	4703
rs754298562	snp	C/T	3.31417e-05	0.00407059	missense, intron-variant	NEB	GRCh38.p7	2:151627539	TCGCTCTGGAGGTCA[C/T]AGGCCTGCCGAGCAT	4703
rs754308213	snp	A/C	1.83984e-05	0.00303296	missense, intron-variant	NEB	GRCh38.p7	2:151616031	CTCTTGAAGCCTTGG[A/C]TGCTTGGATTGGAAT	4703
rs754310164	snp	C/T	3.33561e-05	0.00408374	missense, intron-variant	NEB	GRCh38.p7	2:151610086	GCTCCAATGTGGTGG[C/T]CTTTCTGTTTCTCAT	4703
rs754326721	snp	C/T	3.31444e-05	0.00407076	missense, intron-variant	NEB	GRCh38.p7	2:151640642	GGTGGCCGAGCTGCT[C/T]ACGATAGCCTTCTTT	4703
rs754331413	snp	G/T	1.67072e-05	0.00289021	missense	NEB	GRCh38.p7	2:151692323	CACAGTAATTCATAC[G/T]CTTTGCCTTTGTCTT	4703
rs754340689	snp	A/T	1.82427e-05	0.0030201	missense	NEB	GRCh38.p7	2:151561009	CTCAACTCACACTGC[A/T]GTAAAGATTCTTCAG	4703
rs754340833	snp	C/G	1.7268e-05	0.00293832	missense	NEB	GRCh38.p7	2:151552716	CCTGCACGTAGACTG[C/G]TGTATCTGTGACAAG	4703
rs754341838	snp	C/T	3.31466e-05	0.0040709	missense, intron-variant	NEB	GRCh38.p7	2:151618391	CACTAAGTAATTCTC[C/T]AGCTCTCTTGGCCCT	4703
rs754344015	snp	C/T	1.6582e-05	0.00287936	missense	NEB	GRCh38.p7	2:151655933	CACTGGCATATTCAG[C/T]TGCTTTCTTGGCCTT	4703
rs754354488	snp	C/T	6.17894e-05	0.00555796	missense	NEB	GRCh38.p7	2:151535693	TATTCATACATACCT[C/T]ATTCATCAATTGAGT	4703
rs754360411	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151503462	GAAAATAATTAGAAT[A/G]CCCAGAAAGGTAAAA	4703
rs754365974	snp	A/G	0.000116323	0.00762547	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151492246	CACTGGTGTGAAGCA[A/G]CCCTTGTGTTTCTCA	4703
rs754366347	snp	C/T	0.000286504	0.0119654	missense	NEB	GRCh38.p7	2:151535794	ACTTCTTTATACTTA[C/T]ACTAGAAAAAACAGA	4703
rs754369875	snp	A/G			stop-gained	NEB	GRCh38.p7	2:151562694	GGTGGAAATAGTGTC[A/G]ATACTCCAGGTCACT	4703
rs754379331	in-del	-/TAGTT	1.70185e-05	0.00291701	intron-variant	NEB, RIF1	GRCh38.p7	2:151503318	ATTTTTTATGGGAAA[-/TAGTT]TAGTTTCTTATATGA	4703
rs754384444	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151613889	CATGGAAATGTAAGT[C/G]AATTAAACCTCTTTT	4703
rs754391030	snp	C/G	0.00105652	0.0229597	missense, intron-variant	NEB	GRCh38.p7	2:151579497	CACAGGGATGGAGAT[C/G]TTGGCTTTGTGGTCG	4703
rs754392310	snp	C/G	2.69255e-05	0.00366906	intron-variant	NEB	GRCh38.p7	2:151545879	CAATGACAAGTAAAG[C/G]GTCCTTACCTCACTC	4703
rs754392417	snp	C/T	1.66158e-05	0.0028823	missense	NEB	GRCh38.p7	2:151678069	TAGTCTTTTTTATAC[C/T]CCCGATCTGATTGTA	4703
rs754394858	snp	A/G	1.65795e-05	0.00287914	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151644121	GCGAAAGCCTTCCTT[A/G]TACTTGTACTAGAGA	4703
rs754403972	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151549230	CATGGTGATGTTATA[C/T]CTTCTGCAGTGAAAC	4703
rs754420039	snp	G/T	1.65814e-05	0.00287931	missense	NEB	GRCh38.p7	2:151677994	ACATCCTGGGCTTTC[G/T]TAGCCGCCACGACAT	4703
rs754435179	in-del	-/TTGT			intron-variant	NEB, RIF1	GRCh38.p7	2:151533894	GTTTGTTTTTTGTTG[-/TTGT]TTGTTTATTTTTTGC	4703
rs754439228	snp	A/T	8.10975e-05	0.00636727	intron-variant	NEB	GRCh38.p7	2:151733112	CAGTGTTTTTTTTTT[A/T]AATCTTACCTCCACC	4703
rs754439771	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151670282	CCACCTTCCAAAATC[C/T]GGGGCTAAAATACAA	4703
rs754454398	snp	A/G	1.65594e-05	0.0028774	missense, intron-variant	NEB	GRCh38.p7	2:151640446	TAGTTCTTGTAGTCC[A/G]CATCGCTGACTAAGG	4703
rs754463499	snp	A/G	4.00232e-05	0.00447325	intron-variant	NEB	GRCh38.p7	2:151560745	TGGGAAAATGCATCT[A/G]GTTAGCTTCTGAGTA	4703
rs754481417	snp	A/G	4.97228e-05	0.00498587	intron-variant	NEB, RIF1	GRCh38.p7	2:151506124	TTGTAAATTATCAAA[A/G]GGAGGCAGAAAATAT	4703
rs754485722	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151646666	ATCACTATCATTATT[A/T]TGACACAGAGTCTTA	4703
rs754491465	snp	A/G/T	0.000132913	0.0081511	synonymous-codon	NEB	GRCh38.p7	2:151555042	TTCTTCCCGATATTT[A/G/T]ATCTATAGAGAATAA	4703
rs754495206	snp	C/G			intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151534425	ATGTCATCTCTAGTG[C/G]CGGGCTCCCAACATA	4703
rs754500916	snp	A/C	2.85457e-05	0.00377784	intron-variant	NEB	GRCh38.p7	2:151664898	TGCATGATTTTACAG[A/C]AGGACAAGTTTGACC	4703
rs754502554	snp	C/T	1.67281e-05	0.00289202	intron-variant	NEB	GRCh38.p7	2:151659195	AACAGTGTAAATTAG[C/T]GTTTAAAATCTTAAA	4703
rs754506178	snp	C/T	3.31642e-05	0.00407198	synonymous-codon, intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151534287	CAGGTGGTATTTATC[C/T]TTCCGCTGCTCATAA	4703
rs754513702	snp	C/T	0.00029831	0.0122093	synonymous-codon	NEB	GRCh38.p7	2:151672450	ATGATGCAATGGCTG[C/T]TTGTAGTTGACATTG	4703
rs754546866	in-del	-/AC			intron-variant	NEB	GRCh38.p7	2:151686077	ACAACATTGAAAACA[-/AC]AGTTTGTCTTCGTTA	4703
rs754556124	snp	C/T	6.62581e-05	0.0057554	missense, intron-variant	NEB	GRCh38.p7	2:151627070	TCACACTGGTAAATT[C/T]CAGCTTGTCCGGAGG	4703
rs754556507	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151558055	AATAAACGGTATTCA[A/G]TTAGGAAAAGAGGAA	4703
rs754561099	snp	A/G	1.65924e-05	0.00288027	stop-gained	NEB	GRCh38.p7	2:151697561	CACTACTGAAGTTCT[A/G]CAGAACAGTATCGAG	4703
rs754562358	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151520836	ACCACTGCACTCCAT[C/T]GTGGGCAACAGAGCA	4703
rs754565040	snp	C/T	1.65608e-05	0.00287752	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151633849	GTCCTTTTTGTACTC[C/T]CTGTCACTCTGGATC	4703
rs754579097	snp	A/C	1.66217e-05	0.0028828	intron-variant	NEB	GRCh38.p7	2:151546461	GAGAGGCAAACACAG[A/C]AATATAGCTGGTCAT	4703
rs754580455	snp	C/G	5.04503e-05	0.00502221	intron-variant	NEB	GRCh38.p7	2:151677869	TTGAGAAGTAAATGA[C/G]ACTTACATCACTCTG	4703
rs754591559	in-del	-/C			intron-variant	NEB	GRCh38.p7	2:151554350	AGAATTGCTTGAGCC[-/C]AGGAGTTTGAGACCA	4703
rs754596703	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151508145	ATAAGGAGGGTAAAC[A/G]CCACAGGGATATAGG	4703
rs754604343	in-del	-/TATATATATATATATTTTTTTTTTTTTTTTTTT			intron-variant	NEB	GRCh38.p7	2:151576503	ATATATATATATATA[lengthTooLong]TTTTTTTTTTTTTTG	4703
rs754607487	snp	C/T	1.65608e-05	0.00287752	missense, intron-variant	NEB	GRCh38.p7	2:151627754	CACATGCATGGACCA[C/T]ATCATCTTGGGGTCA	4703
rs754614002	snp	A/C			intron-variant	NEB, RIF1	GRCh38.p7	2:151508993	GCTTAACTTAGCTCC[A/C]GTTTTTCCCACTCTT	4703
rs754624107	in-del	-/T	8.3455e-05	0.00645914	intron-variant	NEB	GRCh38.p7	2:151675441	AAAATCTATTAATTG[-/T]TTTGCTTTAAAGAGT	4703
rs754626202	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151719148	TAATTTTTTGTCTAC[A/G]TGTCTCTTTCCTCTT	4703
rs754635266	snp	G/T	1.65616e-05	0.00287759	missense	NEB	GRCh38.p7	2:151666202	GTGGCAACCTCCTGA[G/T]ATTTCTTTGCAGCTG	4703
rs754635980	snp	C/T	1.68303e-05	0.00290084	synonymous-codon	NEB	GRCh38.p7	2:151551822	GCCTCTGACACTGTG[C/T]ACATAGTCATAGTGG	4703
rs754636584	snp	C/T	2.29745e-05	0.00338921	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151496366	GTTTTCTTTGTATAA[C/T]ACCTGTGCGATGAGA	4703
rs754636819	snp	A/G	1.6588e-05	0.00287988	intron-variant	NEB	GRCh38.p7	2:151655806	GTGTGGACGGCCACT[A/G]TTCTCTGTACCTTGT	4703
rs754636982	snp	A/T	1.65611e-05	0.00287755	missense	NEB	GRCh38.p7	2:151672523	ATGTCCCCAGGGGTA[A/T]GGTAGCTGGTTTTGG	4703
rs754642401	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151682924	TTCTTTGGTGAGATA[C/T]AGTAACAGCTCTTCG	4703
rs754642464	in-del	-/T	1.65798e-05	0.00287917	frameshift-variant	NEB	GRCh38.p7	2:151687428	CTCACATCACTCTGG[-/T]TTTTTGGCTGTCTTC	4703
rs754659395	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151621389	ATTTTTACTAGCAGA[G/T]AACAGTATCATATAA	4703
rs754671742	snp	C/G	1.65946e-05	0.00288046	missense, intron-variant	NEB	GRCh38.p7	2:151612214	AGGGCATTATTCTTT[C/G]CTAGGACAATTTCCG	4703
rs754682378	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151724643	CCGAGTCACAGCTGC[C/G]TCTTTGGGCAGGGCA	4703
rs754685780	snp	A/G	2.11737e-05	0.00325367	intron-variant	NEB	GRCh38.p7	2:151570491	AAGTTAAAAAAGGCC[A/G]CTCACGTCACTGGCA	4703
rs754689425	snp	A/C	6.68293e-05	0.00578015	intron-variant	NEB	GRCh38.p7	2:151723536	TAGGGTCACGTTTAC[A/C]CAAAATACATAGTTT	4703
rs754699796	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151495912	ACAACAAAATCATAT[C/T]TAAGAAAGAGCCGCA	4703
rs754700207	snp	C/T	1.65789e-05	0.0028791	missense	NEB	GRCh38.p7	2:151538163	TGTCATCTGTGACTT[C/T]GCGATGATAGACAAT	4703
rs754711510	snp	A/T	1.65913e-05	0.00288017	missense, nc-transcript-variant, intron-variant	NEB, RIF1	GRCh38.p7	2:151506239	GCCGTTCCTGGTGAG[A/T]CATCCTCTTTATATA	4703
rs754715428	snp	C/G	1.93414e-05	0.00310972	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151526229	CGGCATGGCAGGTTC[C/G]TCTTTCCTTGACATG	4703
rs754726977	snp	A/G	4.57007e-05	0.00477999	intron-variant	NEB	GRCh38.p7	2:151610879	ATGCTACAGGGCAGG[A/G]CGGCATGGGGCATGG	4703
rs754730007	in-del	-/T	1.65814e-05	0.00287931	frameshift-variant	NEB	GRCh38.p7	2:151548321	ACCTCGCTGGTAACA[-/T]TGTTGACTCTCCGGA	4703
rs754735623	snp	A/G	1.6596e-05	0.00288058	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151650209	ATTTGTCTTTGCCAG[A/G]ACTATATCCATGGCA	4703
rs754740854	snp	A/C	9.2477e-05	0.00679926	intron-variant	NEB	GRCh38.p7	2:151592177	AATGGTCAATTAGTA[A/C]ATAAGTCAATTACCA	4703
rs754741351	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151554873	ATGAAATCACATAAC[A/G]AGCGGCACATTTCTC	4703
rs754749029	snp	G/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151524849	ATTTTTGTGTTTTTA[G/T]TAGAGACAGGGTTTC	4703
rs754749448	snp	A/G	1.658e-05	0.00287919	synonymous-codon	NEB	GRCh38.p7	2:151562212	GTCATCTTTATACAC[A/G]TTCTGCAAGAAAGAG	4703
rs754751835	snp	C/G	1.74659e-05	0.0029551	utr-variant-3-prime, intron-variant	NEB, RIF1	GRCh38.p7	2:151485743	GTCCTGCAGACAAGT[C/G]TGATGCTTTGAAATG	4703
rs754761334	snp	A/C	4.55861e-05	0.00477399	missense, intron-variant	NEB	GRCh38.p7	2:151646233	GCTTCTCTATAAAGT[A/C]TCTAAAATAAGAAAT	4703
rs754761980	snp	C/T	1.66454e-05	0.00288486	intron-variant	NEB	GRCh38.p7	2:151642893	AACAGAAAAACATGA[C/T]TGGTATAGGCCAGTA	4703
rs754762324	snp	C/T	1.68134e-05	0.00289938	synonymous-codon	NEB	GRCh38.p7	2:151697634	TGTCTTTTCATAGTT[C/T]TCCTTGTATAGTTTC	4703
rs754764615	snp	A/C	0.00011653	0.00763225	intron-variant	NEB	GRCh38.p7	2:151603791	CATGAAGGAGAGGAA[A/C]ACAGAGTGGGGAAGA	4703
rs754783982	snp	A/G	2.19962e-05	0.00331626	intron-variant	NEB	GRCh38.p7	2:151565689	GGAGGACAGGCATAG[A/G]TTAGAAGGAGAATAG	4703
rs754791239	snp	G/T	1.66021e-05	0.0028811	missense	NEB	GRCh38.p7	2:151663736	TCTCATATCCCTTCT[G/T]GTATTCCCGGTCTGA	4703
rs754819032	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151634338	CACTTGGTAGAATGG[G/T]GTCTTTGATAAACAG	4703
rs754819856	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151622872	CCAGAATTCAGTTCA[A/G]GAGAATGAGTAGCAT	4703
rs754847294	in-del	-/CTC	0.000194129	0.00985022	cds-indel, intron-variant	NEB, RIF1	GRCh38.p7	2:151490448	TGAATGCTCAGACTT[-/CTC]CTCACCCCCACTGAT	4703
rs754848415	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151656978	GAATAGCTTTATATT[C/T]GTGGAGCTCCTTTTC	4703
rs754861799	snp	A/G			upstream-variant-2KB	NEB	GRCh38.p7	2:151735669	TTGGGAGGCCGAGGC[A/G]GGCAGATTGTCTGAG	4703
rs754862510	snp	A/C			intron-variant	NEB, RIF1	GRCh38.p7	2:151496727	CATTTTTAAAAAATG[A/C]TTGAAAATATCAGAT	4703
rs754865589	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151657785	AGGGAGCTGACATCT[A/G]TGAGGGTCACCATGT	4703
rs754872432	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151661095	GGTGCTTTGCTTCTC[C/T]GGGCTGTTCTTTTCT	4703
rs754874791	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151688569	CTATTTCAGGGACTG[C/T]GGCACAGTCCTCCTT	4703
rs754876542	snp	C/G	3.33378e-05	0.00408262	intron-variant	NEB	GRCh38.p7	2:151562062	ACTGACACCACCATG[C/G]ATTCTGATGACCCAT	4703
rs754876825	snp	C/T	0.000104511	0.00722806	intron-variant	NEB	GRCh38.p7	2:151614630	GACAAGAACATCTTA[C/T]ATAATCATGTTTCAT	4703
rs754891682	snp	A/G	4.73003e-05	0.00486291	intron-variant	NEB	GRCh38.p7	2:151568048	CCACTTTTGCAAAAT[A/G]CACTCCCATCAGGAT	4703
rs754895962	snp	A/G	1.66333e-05	0.00288381	splice-donor-variant, intron-variant	NEB, RIF1	GRCh38.p7	2:151503347	GATATATTTGTAAAT[A/G]CCGAGCTAAAGTTCT	4703
rs754896798	snp	A/G	1.6571e-05	0.0028784	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151525223	TGGCTCCAGCATGAT[A/G]GAGTAGTTGGATTTT	4703
rs754903293	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151529024	CTTTGCTCTTCCCTA[C/T]GCTCCTTTGTGAGGA	4703
rs754906199	snp	C/G	2.77982e-05	0.00372805	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151621021	CATGGCCTGACGATA[C/G]AGGCTCTGAGGAAAG	4703
rs754906897	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151637109	TTGAGACCCCTCTCA[A/T]CCTAAAGGTTCCTGG	4703
rs754914675	snp	C/T	1.65949e-05	0.00288048	synonymous-codon	NEB	GRCh38.p7	2:151663833	GTGTTTCCCTTTGGC[C/T]TGTTCATAGGCTTTC	4703
rs754923566	snp	G/T	1.65792e-05	0.00287912	intron-variant	NEB	GRCh38.p7	2:151620870	ATCCAGCTGTATTCT[G/T]TGTGGCTGGCATGAT	4703
rs754933341	snp	A/G	0.000142288	0.00843349	intron-variant	NEB	GRCh38.p7	2:151675250	ATAATTTTATTGTCA[A/G]GTCCGAATTTCACAT	4703
rs754944482	snp	G/T	2.13723e-05	0.0032689	missense	NEB	GRCh38.p7	2:151565097	TATGTGGTGTATCTG[G/T]TGAAAACGTATATTT	4703
rs754953272	snp	A/C	3.41629e-05	0.00413283	intron-variant	NEB	GRCh38.p7	2:151694640	AGATTCTGGACAAAA[A/C]AATTCAGCAAAGGAA	4703
rs754959175	snp	C/T	0.00010176	0.00713231	missense	NEB	GRCh38.p7	2:151690822	GATGAACTTTGTAGG[C/T]ATGCTAGAAAAGAAG	4703
rs754970992	snp	C/T	1.65619e-05	0.00287762	missense	NEB	GRCh38.p7	2:151697355	TAGAACTTACATCAC[C/T]GTTTTGAGCTGTGAC	4703
rs754972801	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151729795	GGTAGGTGAGGGAGC[C/T]TGTTCATATTTTGGA	4703
rs754978861	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151676656	ACTGCTGTTATATTG[C/T]TCCTTTTGCCAGGAA	4703
rs754985496	snp	A/C	1.65688e-05	0.00287821	missense	NEB	GRCh38.p7	2:151553921	CAGGCGGTAATCAAT[A/C]TCACTGACTTTCTTC	4703
rs754985741	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151689897	TCTTTACTAATTGGG[C/T]ATGAGCTAATTTGTG	4703
rs754993589	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151517396	CAGAAGACACGAGGA[C/T]GTTTCTAATAGTTAG	4703
rs755003638	snp	C/T	1.66768e-05	0.00288758	missense	NEB	GRCh38.p7	2:151662337	TAGTCAGCCTTGTAC[C/T]GATTCTGCAAAAGAG	4703
rs755005542	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151713995	TATGGCTCCCTAGTA[A/T]AATGAGTATTTTGAA	4703
rs755007581	in-del	-/TTTTTTTTT			intron-variant	NEB, RIF1	GRCh38.p7	2:151512021	TTACCCTCTCACTCT[-/TTTTTTTTT]TTTTTTTTTTTTTTT	4703
rs755009242	snp	A/G	4.40733e-05	0.00469411	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151491745	TCATAGTCAAAAACC[A/G]AACCAGGATTAGTAC	4703
rs755009988	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151591110	TTGTAAATTAAGTGA[C/T]ATTGTGAAGATATTG	4703
rs755028230	snp	C/T	7.22517e-05	0.00601005	intron-variant	NEB	GRCh38.p7	2:151549589	TTAATATGAGTCTCC[C/T]GCCACCCCACCTTCA	4703
rs755030833	snp	C/T	3.48888e-05	0.0041765	intron-variant	NEB	GRCh38.p7	2:151639831	CTTTAGGAGCCCCAC[C/T]TCGATTCTTAATTTT	4703
rs755041913	snp	A/C	1.77998e-05	0.00298321	intron-variant	NEB	GRCh38.p7	2:151666068	ATTAGAAATGGATAA[A/C]AACTTGGTAACCAGT	4703
rs755045379	snp	A/T	2.01015e-05	0.00317023	intron-variant	NEB	GRCh38.p7	2:151717554	GGGATGTATTTTAAA[A/T]ACGATTATGCTTTCA	4703
rs755046176	snp	G/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151503880	TTTTTGTTTTGTATG[G/T]TCTAATGAATGTTCC	4703
rs755060324	snp	A/G	2.50466e-05	0.00353874	synonymous-codon	NEB	GRCh38.p7	2:151665519	TTTCATCCAATTGGT[A/G]AAGTCAGATTTGTAC	4703
rs755064162	snp	C/T	3.79097e-05	0.00435355	intron-variant	NEB, RIF1	GRCh38.p7	2:151496266	GTTTTTTTCTTTTCT[C/T]GCCAAGTACCGAGCT	4703
rs755069446	snp	A/G	1.65616e-05	0.00287759	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151627565	AGCATGGATGACATC[A/G]TTCTGGTCGGGCAGG	4703
rs755069615	in-del	-/AG	1.66179e-05	0.00288248	intron-variant	NEB, RIF1	GRCh38.p7	2:151524645	GAAAATGTTTACTCA[-/AG]AGAGAGGCTTTTTTT	4703
rs755072735	snp	A/G	3.35284e-05	0.00409427	intron-variant	NEB, RIF1	GRCh38.p7	2:151491656	AATGGTGATGTTTAT[A/G]TTGTAAGCCTTTTTC	4703
rs755078182	snp	C/T	1.71646e-05	0.0029295	intron-variant	NEB	GRCh38.p7	2:151535834	CTTGACAGCAGGCTA[C/T]GATTATCTTAAGAAT	4703
rs755100778	snp	A/G	0.000352423	0.0132698	intron-variant	NEB	GRCh38.p7	2:151581456	GCAGAGAGCACTGTG[A/G]AAAGCAAATGATGTG	4703
rs755102106	snp	A/C	0.000153331	0.00875454	intron-variant	NEB	GRCh38.p7	2:151546027	AAAAAAACAGAAATA[A/C]AAGTTGATTAATCAT	4703
rs755105815	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151536040	GCCTCCCAAGTAGGT[A/G]GGACTACAGGTTGTA	4703
rs755106823	snp	A/G	3.3315e-05	0.00408122	intron-variant	NEB	GRCh38.p7	2:151644427	TGCTTTGAAGTGATA[A/G]ATTGCAATCAAATCA	4703
rs755107450	in-del	-/CTTT			intron-variant	NEB	GRCh38.p7	2:151691456	TTTCTGTGCTCCTTC[-/CTTT]GTTTATTACTTGTCT	4703
rs755110823	snp	C/T	3.64564e-05	0.0042693	intron-variant	NEB, RIF1	GRCh38.p7	2:151518941	GTAAAACAAGCTGTT[C/T]CTGGAGCAAATGACT	4703
rs755135440	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151728935	AAATTACAGCATCTA[C/T]AGATACTAGTTTTTA	4703
rs755139831	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151504754	AAAAGGGGTGGGTGC[A/G]GAGCCAGGGCTTGCT	4703
rs755153044	snp	A/T	0.000232063	0.0107693	missense	NEB	GRCh38.p7	2:151549696	AGTGTCACCTGGAAG[A/T]CTATATCCAGTGGGC	4703
rs755153443	snp	C/T	2.09466e-05	0.00323618	missense	NEB	GRCh38.p7	2:151545905	CACTCAGATGTGTCT[C/T]CAGTTCTTGCACTTT	4703
rs755161771	snp	C/T	1.71557e-05	0.00292875	intron-variant	NEB	GRCh38.p7	2:151674449	CAAAAAGGCAAACAC[C/T]TAAACTTCACCTAAA	4703
rs755164442	snp	A/C	1.76577e-05	0.00297129	missense, intron-variant	NEB	GRCh38.p7	2:151642677	AGGCCAAGCTTATAC[A/C]ATTTCTAAAATAGAC	4703
rs755165133	snp	C/T	6.68416e-05	0.00578068	missense	NEB	GRCh38.p7	2:151537184	AAATCAGGGGTATCA[C/T]AGGCATAGCAACCAA	4703
rs755169922	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151715145	TACCCAACACTGTCA[C/T]CTTGCCCACCTAGAG	4703
rs755176537	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151550588	TCTTAAATACTCTGT[C/G]TCTTGGAGTTTAGGA	4703
rs755185189	snp	C/T	1.65614e-05	0.00287757	missense	NEB	GRCh38.p7	2:151694388	CATTAATGCTGAGGA[C/T]TCCAATCATTTTCCC	4703
rs755195025	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151649396	GTAAAGTGTATAGCA[C/T]ATTACATATAGTATA	4703
rs755199802	snp	A/T	1.68125e-05	0.00289931	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151519043	CACGGGTTTGTGAAG[A/T]TTCTTCAGGTCAGCC	4703
rs755212048	snp	C/T	1.78156e-05	0.00298454	intron-variant	NEB	GRCh38.p7	2:151619448	AACATCAAGGAAACT[C/T]ACGTCACTCTGGAGG	4703
rs755213444	snp	C/T	2.63584e-05	0.00363022	intron-variant	NEB	GRCh38.p7	2:151561180	AAGAAATAGTTTGTC[C/T]CTGGAAGAGGAGTAC	4703
rs755223820	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151716287	GAGATTACAGGCGCC[C/T]GCCACCACGCCTGGC	4703
rs755225703	snp	G/T	0.000132864	0.0081495	intron-variant	NEB, RIF1	GRCh38.p7	2:151491659	GGTGATGTTTATGTT[G/T]TAAGCCTTTTTCAGC	4703
rs755228645	snp	C/T	1.65756e-05	0.00287881	synonymous-codon	NEB	GRCh38.p7	2:151725468	CTCACTGAGTTGATC[C/T]TGTACTTTTTTGATT	4703
rs755229024	in-del	-/TG	2.63953e-05	0.00363276	intron-variant	NEB, RIF1	GRCh38.p7	2:151527462	GCAGTTACAATCGTC[-/TG]TGTCTCTCCTGTCTT	4703
rs755231047	snp	G/T	1.84517e-05	0.00303735	missense	NEB	GRCh38.p7	2:151570150	CATGCAGGTCCACTG[G/T]TGCAGGTAATTGCGG	4703
rs755239192	snp	C/T	9.92113e-05	0.00704243	splice-donor-variant, intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151499297	TTTTATTTTTAAATA[C/T]CGAACTAAAGTTTTC	4703
rs755239726	snp	A/T	1.65638e-05	0.00287778	missense	NEB	GRCh38.p7	2:151697429	TAATGTCCCAAAATA[A/T]CTTTTAAGTAGGAAT	4703
rs755241089	snp	A/G	2.01205e-05	0.00317173	intron-variant	NEB, RIF1	GRCh38.p7	2:151512700	TCTTTCATGATTGGG[A/G]TTTATGAGTGATGGC	4703
rs755252426	snp	C/T	1.68012e-05	0.00289833	missense, intron-variant	NEB	GRCh38.p7	2:151642587	ACTTCACTTGCAATA[C/T]CTCTGGAGGCCTTGG	4703
rs755252809	in-del	-/A	0.5	0	intron-variant	NEB	GRCh38.p7	2:151570459	CTAGGGCATCGGCTG[-/A]AAAAAAAAAAACTGA	4703
rs755268228	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151537097	TACAGGTATATGTCG[A/G]ATGGATGAGGCCAAT	4703
rs755269650	snp	A/C	0.000475342	0.0154092	intron-variant	NEB	GRCh38.p7	2:151679672	TCAGACCCCAAGCCC[A/C]CCCACCCACATTTTC	4703
rs755272145	snp	C/T	1.68792e-05	0.00290505	missense	NEB	GRCh38.p7	2:151663565	CACTTTGAATCTGCA[C/T]CATATTTTTGGCCAA	4703
rs755284958	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151651071	ATTTACAGGTACATG[C/T]CACCTCATCCAGCTT	4703
rs755288635	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151571378	TCGTTCATAAAAAGG[A/G]TTTGGCTTTGTTTTC	4703
rs755291072	snp	C/T	2.09633e-05	0.00323747	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151636329	ATTAGCAAGTTTGTA[C/T]AGACTCTAAATTTGG	4703
rs755291524	snp	C/T	1.65737e-05	0.00287864	missense	NEB	GRCh38.p7	2:151656343	TCATAGTTTTTCTTG[C/T]ACTCCCGATCAGATT	4703
rs755292193	snp	A/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151522636	CACAAAAATCAACAG[A/T]AAAGAATGCAACCTG	4703
rs755294228	snp	A/C	2.33348e-05	0.00341568	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151508057	ATCTCTGGGGTGTCC[A/C]AAACAGTCTCATAAT	4703
rs755307254	snp	A/G	1.65614e-05	0.00287757	synonymous-codon	NEB	GRCh38.p7	2:151562731	GTACTGGCACCTTTT[A/G]GCCAGCACGTGATTC	4703
rs755311694	snp	C/T	1.65614e-05	0.00287757	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151524529	CCTCACTGGCCTGTT[C/T]GGCTGCCTGTGTGGC	4703
rs755314719	snp	C/T	4.97104e-05	0.00498525	missense, intron-variant	NEB	GRCh38.p7	2:151618357	TTCAGCGTTTCTGGA[C/T]GCTGACGGTAGATAG	4703
rs755319612	snp	C/T	1.73399e-05	0.00294443	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151493364	ATACCGAGCTAATGT[C/T]TTCTTGGTTGCGCTT	4703
rs755325245	snp	C/T	9.18695e-05	0.0067769	intron-variant	NEB	GRCh38.p7	2:151630693	ACCACCACAATATAG[C/T]ACCACAGATTTTTGC	4703
rs755335251	snp	C/G	1.66852e-05	0.0028883	missense	NEB	GRCh38.p7	2:151567378	TCTCTCATTCTGAAT[C/G]TGGCCTGCATGCTCA	4703
rs755351248	snp	C/T	1.65723e-05	0.00287852	missense	NEB	GRCh38.p7	2:151674502	ATGTTTCTCGATGCC[C/T]TGGCTGCAGTGATGG	4703
rs755370356	snp	C/G/T	0.00011757	0.00766631	missense	NEB	GRCh38.p7	2:151547668	GTCTTCTTGACTTGG[C/G/T]GGATCTCAGGGGTAT	4703
rs755374717	in-del	-/TA			intron-variant	NEB, RIF1	GRCh38.p7	2:151502602	AAAGTGATAAATATC[-/TA]TGTTTTAGAGAAAAC	4703
rs755378494	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151556727	CAAGTTCTTGGAGAC[A/C]TACAGAGAGACTTAG	4703
rs755388476	snp	G/T	1.79258e-05	0.00299376	missense, intron-variant	NEB	GRCh38.p7	2:151650575	TAATAGAAACTGACC[G/T]CACTTTGCAGTTCAT	4703
rs755389282	snp	C/T	1.6819e-05	0.00289987	missense	NEB	GRCh38.p7	2:151688366	TATGGCACTTGAACT[C/T]CTCACCTTCATGTTT	4703
rs755390933	snp	C/G	9.94052e-05	0.00704931	missense, intron-variant	NEB	GRCh38.p7	2:151614344	GCAGGCAGGTCCATT[C/G]ATGCAGGGGATGCTT	4703
rs755392031	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151644267	CTTTTGATAAGAAAG[A/G]TTAAAGGCTAAATTC	4703
rs755394940	snp	C/T	1.65814e-05	0.00287931	missense	NEB	GRCh38.p7	2:151656254	AGTTAGTGTTGGTGA[C/T]GTTGGCTTGGGCATC	4703
rs755407242	snp	C/T	1.6585e-05	0.00287962	missense	NEB	GRCh38.p7	2:151553469	CGTAGCAACCAATGC[C/T]TTTCAGCCAGTTGAG	4703
rs755408282	snp	C/T	1.91521e-05	0.00309446	intron-variant	NEB, RIF1	GRCh38.p7	2:151493464	GGGAAGCCAAAAGAG[C/T]ATCTAGGCATCAGAC	4703
rs755422317	snp	A/G	2.18272e-05	0.0033035	intron-variant	NEB, RIF1	GRCh38.p7	2:151516438	GGATCATTGTTGTGT[A/G]GTGTGGTTTTTTTGA	4703
rs755427627	snp	A/T	1.76462e-05	0.00297032	missense	NEB	GRCh38.p7	2:151667907	CAATCTGCTTTATAA[A/T]GAGCCTTCAAAAAAG	4703
rs755428873	snp	C/T	1.65693e-05	0.00287826	missense, intron-variant	NEB	GRCh38.p7	2:151627006	TGGGGGCTCACCTTG[C/T]TCATATTGAGAGCAT	4703
rs755457782	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151685038	TCCAGAAAAGACAGA[G/T]ATCTTTCATAAACAA	4703
rs755457824	snp	C/T	3.31538e-05	0.00407134	missense	NEB	GRCh38.p7	2:151567257	AGTAATTACGATAAT[C/T]AATATCACTGACAAG	4703
rs755465698	snp	A/T			intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151498983	AGTCGGATCTTTGCA[A/T]AATACATTTGTTTAA	4703
rs755467658	snp	C/G	1.65627e-05	0.00287769	missense	NEB	GRCh38.p7	2:151680809	AACTTGAGGGTGTCT[C/G]GATGTTGGCGATATT	4703
rs755468871	snp	A/G	3.32044e-05	0.00407444	missense	NEB	GRCh38.p7	2:151576206	TCAGGTGTGTCAACA[A/G]TGCTTGTGTACTTAA	4703
rs755471043	snp	A/G	8.7447e-05	0.0066118	intron-variant	NEB	GRCh38.p7	2:151562848	AAGAAAGGGGTTTAA[A/G]TGTAAATTATTCAGA	4703
rs755477517	snp	C/T			utr-variant-5-prime	NEB	GRCh38.p7	2:151733787	CGTTTCTGTAGCTCT[C/T]GTTCAAACCTGAAAA	4703
rs755477956	snp	C/T	3.31214e-05	0.00406935	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151614459	CCACTTCTCAAACTC[C/T]TTCTTGTACTCCCTG	4703
rs755492414	snp	C/T	1.6855e-05	0.00290297	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151534176	GAGAAACTGGGAGCA[C/T]AGTCCTGCCTGGGCC	4703
rs755494167	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151707543	TGGAGCAGGGAGAAG[A/G]AGCCTTGCTTTTCCT	4703
rs755508128	snp	C/T	1.65866e-05	0.00287976	missense	NEB	GRCh38.p7	2:151710457	TGTTATCAGCATTCA[C/T]TCTGGCATTTGCAAC	4703
rs755513692	snp	A/G	9.1295e-05	0.00675568	intron-variant	NEB	GRCh38.p7	2:151690669	CATGTAAATGCTTAC[A/G]TTTTAAATGAGCAAA	4703
rs755517435	snp	C/T	5.62003e-05	0.00530066	intron-variant	NEB	GRCh38.p7	2:151709648	TAAATGGGATGATTT[C/T]CTCATACCTTGCTAG	4703
rs755521679	snp	A/G	0.000138153	0.00831007	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151609851	TGCTTGGATAATGTC[A/G]TTTTGATCCGGCATG	4703
rs755531536	in-del	-/C	1.65616e-05	0.00287759	frameshift-variant	NEB	GRCh38.p7	2:151694370	GCAGCATCTTGGGAT[-/C]GTCATTAATGCTGAG	4703
rs755542829	snp	C/T	1.65902e-05	0.00288008	synonymous-codon	NEB	GRCh38.p7	2:151540772	GTGATGATGGGGTCT[C/T]TCTTTGGTGGCAAGT	4703
rs755544084	snp	C/T	1.65696e-05	0.00287828	intron-variant	NEB, RIF1	GRCh38.p7	2:151524623	GTAAGCGACCTTTAT[C/T]GGGGAAGAAAATGTT	4703
rs755548124	snp	C/T	6.57052e-05	0.00573134	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151514832	CCTCGCTTGCTATTT[C/T]AGTTGCATATTTGAC	4703
rs755554259	snp	A/G	1.83981e-05	0.00303294	synonymous-codon	NEB	GRCh38.p7	2:151724296	CTTAACGGCCTGGAC[A/G]AGTTCAGGGGCATCA	4703
rs755562712	snp	C/G	2.14576e-05	0.00327542	intron-variant	NEB	GRCh38.p7	2:151565705	TTAGAAGGAGAATAG[C/G]CTTTGCGTACCTGAC	4703
rs755565215	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151512896	CACAACAGTTGTTGG[C/T]TTGATTTGATTAAGA	4703
rs755578871	in-del	-/T			frameshift-variant, intron-variant	NEB	GRCh38.p7	2:151654061	TGGGAGATCATAGCC[-/T]TTCTTCAAAGCTTCT	4703
rs755582434	snp	A/G	1.7042e-05	0.00291903	intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151497040	GTATAACACCTGTGC[A/G]ATAAGAAAGCAACCA	4703
rs755600124	snp	G/T	6.11639e-05	0.00552976	missense, intron-variant, utr-variant-3-prime	NEB, RIF1	GRCh38.p7	2:151497647	AATATTTTCTTGATT[G/T]TGTTTGACTCTTTCC	4703
rs755604172	snp	C/T	1.65608e-05	0.00287752	missense, intron-variant	NEB	GRCh38.p7	2:151633872	TCTGGATCTTGGCTA[C/T]GTGCATGGACCACAT	4703
rs755614432	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151503555	ATCTAGCTCTCAAAT[A/G]TAACATTCAAGGAAC	4703
rs755616084	snp	A/C	1.65619e-05	0.00287762	missense	NEB	GRCh38.p7	2:151666294	GTACTCACGATCAGA[A/C]TGGATTTTGGCCACA	4703
rs755620162	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151683011	AATGGAAGTCTGTGG[C/T]ACTCTAATTCCAACC	4703
rs755621643	snp	A/C/G	9.94455e-05	0.00705081	missense, intron-variant	NEB	GRCh38.p7	2:151643846	TCATAGGCCTGCCGA[A/C/G]CATGGATGACATCGC	4703
rs755631301	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151722366	TCAAGCCTAAGGACT[C/G]TGTTAAGCCTTTTAA	4703
rs755633016	snp	C/T	1.69902e-05	0.00291458	missense	NEB	GRCh38.p7	2:151551832	CTGTGCACATAGTCA[C/T]AGTGGTAGACAGCCT	4703
rs755634045	snp	C/T	1.65756e-05	0.00287881	synonymous-codon	NEB	GRCh38.p7	2:151655841	GGTATGTGCATTCTG[C/T]TTGGCAAGCACCATG	4703
rs755653889	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151539926	TATCACAATTCTCAT[C/T]ATCATTCCACATATA	4703
rs755659279	snp	G/T	3.31796e-05	0.00407292	missense	NEB	GRCh38.p7	2:151662229	GGGTGCTGGCGGTAC[G/T]TCTTTTCACTAATAA	4703
rs755660001	snp	C/T	3.60887e-05	0.00424771	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151526953	TCCTGAGGGCGAGCA[C/T]CGTGTTTTTGTCATC	4703
rs755665857	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151720484	GCCTTAACTGTCACA[C/T]CTTTTTGAGGAATAG	4703
rs755673215	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151641542	TGCTATGTTGACCAG[C/G]CTGGTCTCAAACTCC	4703
rs755681001	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151669976	AGGTACTGCATGTGG[G/T]AGTTCACACAGGGAG	4703
rs755686393	snp	A/G	1.68182e-05	0.00289979	missense	NEB	GRCh38.p7	2:151666395	CGTAGGCCTCCTTAT[A/G]TTTGCACTATTTGAA	4703
rs755692441	in-del	-/CT	3.53232e-05	0.00420242	intron-variant	NEB	GRCh38.p7	2:151551716	GATTTCTGCTGGGCA[-/CT]CTCAAGTTCTCACTG	4703
rs755693888	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151621743	CATATATACCAATGG[A/C]TTTTAGCCCTTTTTG	4703
rs755695934	snp	C/T	1.6563e-05	0.00287771	missense	NEB	GRCh38.p7	2:151687475	TTGGATCGTCATTAA[C/T]GCTGAGGGCTCCAAT	4703
rs755703654	snp	A/C			intron-variant	NEB, RIF1	GRCh38.p7	2:151496060	GTTTTATAGGAAAAT[A/C]TGTTACTTCTTGATA	4703
rs755707288	snp	C/T	2.55764e-05	0.00357597	missense	NEB	GRCh38.p7	2:151535713	ATCAATTGAGTTGCA[C/T]ACTTGAAATGCCTAT	4703
rs755708498	snp	C/G	1.65641e-05	0.00287781	missense, intron-variant	NEB	GRCh38.p7	2:151629580	TGGCAGCCACGATGG[C/G]GATGGCGTCACTTCG	4703
rs755711568	snp	A/G	4.9831e-05	0.00499129	intron-variant	NEB	GRCh38.p7	2:151538248	TTTGTAGCGTAGCTA[A/G]AAAGAGAAAAAACAC	4703
rs755719180	snp	A/G			upstream-variant-2KB	NEB	GRCh38.p7	2:151735451	TCTGTCCTTACACAC[A/G]GCGACAGAAATCACA	4703
rs755729476	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151635817	CAAGCACCGCATGTG[C/T]TTTAAAATACTATCT	4703
rs755734109	snp	G/T	2.15459e-05	0.00328215	synonymous-codon	NEB	GRCh38.p7	2:151565791	CCAGCCAATGCCTCG[G/T]AGCCACTCCAGGTCA	4703
rs755734122	snp	C/T	3.15333e-05	0.0039706	synonymous-codon	NEB	GRCh38.p7	2:151706905	GGCATCTCCTGCTGC[C/T]TTCAGCTGCCTAAGC	4703
rs755736894	snp	G/T	6.45307e-05	0.00567989	intron-variant	NEB, RIF1	GRCh38.p7	2:151513723	AAAGAAAAAAAAAAG[G/T]TACCTAAATGCTACT	4703
rs755738112	snp	C/G	2.32382e-05	0.0034086	missense	NEB	GRCh38.p7	2:151560696	AGGCCTCCTTGTACA[C/G]GTTCTGCAGGAATTA	4703
rs755738831	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151541941	ATTAAGCCTTTTCCA[C/G]TCTCTAGCCAATGGC	4703
rs755753727	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151708326	ATATCTTCAATTTCC[C/G]TCTTTTCATTCACTT	4703
rs755759817	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151543833	TGTGTATTATATTTC[C/T]CCTGTACTTAGGTAT	4703
rs755768805	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151670942	GATGCATCCTCACAC[A/G]TTGAATTAAGAAGGA	4703
rs755791156	snp	A/G	3.32016e-05	0.00407427	missense	NEB	GRCh38.p7	2:151663745	CCTTCTTGTATTCCC[A/G]GTCTGACTGCATCTT	4703
rs755793871	snp	A/G	0.000645599	0.017955	missense	NEB	GRCh38.p7	2:151547455	TGTCTCCCACATAGC[A/G]GCAATGGATCACTTG	4703
rs755796377	snp	A/C	1.67553e-05	0.00289437	intron-variant	NEB	GRCh38.p7	2:151627860	GGTGGTCATTTCAAA[A/C]ATAAAAATGAATAGA	4703
rs755800924	snp	A/G	1.65828e-05	0.00287943	intron-variant	NEB	GRCh38.p7	2:151554042	TGTAAAGTTAAAATC[A/G]CATGCCAGTTATACA	4703
rs755804203	in-del	-/CTC	2.16364e-05	0.00328903	cds-indel	NEB	GRCh38.p7	2:151562623	TACATCACTCAAGAT[-/CTC]CTGGGCGTTTCGGAC	4703
rs755804753	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151577638	CAGGCTGGAGTGCAG[G/T]GGCAATCTCGGCTCA	4703
rs755814962	snp	G/T	1.78121e-05	0.00298425	intron-variant	NEB	GRCh38.p7	2:151568205	AGCCACCATAAAGGG[G/T]TAAAATGAGGAGTCA	4703
rs755817533	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151623349	TCTATAAAGCTTTAT[A/C]ATCCCTCTACTTTAT	4703
rs755820638	snp	C/G	4.97632e-05	0.0049879	intron-variant	NEB	GRCh38.p7	2:151562227	ATTCTGCAAGAAAGA[C/G]AGAACAATGAAATGT	4703
rs755822172	in-del	-/TTC	1.65644e-05	0.00287783	cds-indel, intron-variant	NEB, RIF1	GRCh38.p7	2:151492196	CTGAAGTCCTGCATG[-/TTC]TTCTTTACTCGTTCA	4703
rs755850940	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151712973	TTGGAAGAAAGAGTC[A/G]GTTTCACTTCTCTAG	4703
rs755853362	snp	C/T	6.29875e-05	0.00561158	missense	NEB	GRCh38.p7	2:151658021	CCTTGGCAGCTTTGA[C/T]AGGAATTGCATCAGG	4703
rs755863625	in-del	-/CT	8.70208e-05	0.00659567	frameshift-variant, intron-variant	NEB, RIF1	GRCh38.p7	2:151494190	CTTGATTGCGTTTGA[-/CT]CTCTGCATCTCAGGA	4703
rs755864993	snp	C/G	5.60386e-05	0.00529303	intron-variant	NEB	GRCh38.p7	2:151687621	GGTCCCCAGGCCACA[C/G]TCACATCGCTGGTGT	4703
rs755866825	in-del	-/TACT			intron-variant	NEB	GRCh38.p7	2:151696528	GTTTAAACTTGCTAA[-/TACT]TACTTAGCCTTTTGA	4703
rs755867355	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151529132	GCTGAATTGCCTGAA[A/G]AGATGTAAAAAGAGG	4703
rs755868416	snp	A/G	0.000587865	0.0171344	intron-variant	NEB	GRCh38.p7	2:151570648	GATTCAAATTTGCCA[A/G]TACCTTCAATGGCTC	4703
rs755871388	snp	G/T	1.66081e-05	0.00288163	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151612294	CTTCCTGTCACTCAG[G/T]ATTTCTCCAGCTCTC	4703
rs755875238	snp	G/T	0.00332225	0.0406213	missense, intron-variant	NEB	GRCh38.p7	2:151594258	ACTTGGGGTCATCTT[G/T]TAGGGTGCGGAAACC	4703
rs755877926	snp	A/C	1.65649e-05	0.00287788	missense	NEB	GRCh38.p7	2:151671116	TGGGTGCTGTCGATA[A/C]TTCCTCTCATTTAAT	4703
rs755883171	snp	A/G	6.63119e-05	0.00575774	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151643291	ATTTTTCTCATCCTC[A/G]AGAGAACCACTAGTC	4703
rs755888789	snp	G/T	1.65614e-05	0.00287757	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151514335	CATTGAGGATTTGAG[G/T]GGCATTCTTTGCTCT	4703
rs755894828	snp	A/G	0.000281529	0.0118611	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151643195	CAAAACCATTGGTAT[A/G]GAATCCATAAGGCTG	4703
rs755901684	snp	C/T	1.69493e-05	0.00291108	intron-variant	NEB, RIF1	GRCh38.p7	2:151519807	AATTATTCCTGGACA[C/T]CAATCAATTTGGGAA	4703
rs755915064	snp	A/G	3.32973e-05	0.00408014	synonymous-codon	NEB	GRCh38.p7	2:151677583	ACTGACTTGCTTCGT[A/G]TTCTGTTTTGCCTGG	4703
rs755926453	snp	C/T	1.65619e-05	0.00287762	synonymous-codon	NEB	GRCh38.p7	2:151575761	TGGCATTATGTGTAT[C/T]GAAGTTTTATCCTTG	4703
rs755926462	snp	C/T	1.66117e-05	0.00288194	synonymous-codon	NEB	GRCh38.p7	2:151727757	GAACTTTGAAGGATC[C/T]ACTTTCTTCCGGATG	4703
rs755934851	snp	A/G	1.66468e-05	0.00288498	intron-variant	NEB, RIF1	GRCh38.p7	2:151485946	TTTCTATTCGTGGGG[A/G]TGGAAAAGGGGAAAT	4703
rs755943261	snp	A/G	1.70758e-05	0.00292192	intron-variant	NEB	GRCh38.p7	2:151621066	AAATATAGAATTCAC[A/G]TTCACTCGAAAAGTA	4703
rs755955081	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151690066	CACCTAGGAGCTTAT[C/T]AGAAAGTCAGAATAT	4703
rs755956903	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151530162	TATTTGATGAATGAA[C/T]GAACTGATGAATACA	4703
rs755957294	snp	G/T	2.09641e-05	0.00323753	missense	NEB	GRCh38.p7	2:151658024	TGGCAGCTTTGATAG[G/T]AATTGCATCAGGTCT	4703
rs755966351	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151609682	AAACAATGTGAATGG[C/T]ACCCCCAGCCCCACC	4703
rs755970391	snp	A/G	4.98649e-05	0.00499299	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151503350	ATATTTGTAAATACC[A/G]AGCTAAAGTTCTCTT	4703
rs755973658	snp	A/G	1.68159e-05	0.0028996	intron-variant	NEB	GRCh38.p7	2:151663869	TTTGTACTGTGGACA[A/G]AGAAGAAATTATGGT	4703
rs755976297	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151643441	ATCATTTGCCCCTAA[A/G]TAAAAGTTCATATTA	4703
rs755977726	snp	C/T	0.00031746	0.0125948	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151607513	ACTTACATTGCTGAT[C/T]TGCAAGGCATTGATG	4703
rs755982851	snp	A/G	1.65641e-05	0.00287781	missense	NEB	GRCh38.p7	2:151553958	TCCTTGGCAGTAACC[A/G]TCTCTACCATGTCGG	4703
rs756000690	snp	C/G	1.66896e-05	0.00288869	missense	NEB	GRCh38.p7	2:151671186	CCAATAGGGATCCAT[C/G]CGATGCCCTTCAAGA	4703
rs756001037	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151486015	TTGTAAGATCTCTCA[C/T]GACTGACTCCACAAA	4703
rs756001738	snp	C/T			missense, intron-variant	NEB	GRCh38.p7	2:151644491	CAATTTCCCGGGAGG[C/T]TTTTGCTGCTTTGAT	4703
rs756002873	snp	A/T	0.000184064	0.00959156	intron-variant	NEB	GRCh38.p7	2:151680043	AGAGAAAAAAATGCA[A/T]AAACAAACAAATAAA	4703
rs756011050	snp	A/T	1.65608e-05	0.00287752	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151526015	CCGGGTCTCTGGTAG[A/T]GTTGTGTATGAGCCC	4703
rs756013849	snp	A/G	2.20276e-05	0.00331863	intron-variant	NEB	GRCh38.p7	2:151695697	ACTATGACAGAGAGA[A/G]AACCAATTAGTTCAG	4703
rs756023078	snp	A/G			missense	NEB	GRCh38.p7	2:151549734	GCAGGCTGGTTTTGT[A/G]TAGATTCTGCAGGAA	4703
rs756024407	snp	C/T	1.65688e-05	0.00287821	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151485816	TGCCAGTCCTCTGCA[C/T]AGTGCCATACATCCA	4703
rs756025635	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151631850	AAATTACATGAATAA[C/G]AGTGGGTTTTTCTAG	4703
rs756040800	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151691354	ACCTAAGACGCCCAT[C/T]CAGTCACTGTCTCAC	4703
rs756041236	snp	A/G	3.03255e-05	0.00389382	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151494219	GGAGTGACAGGGGTT[A/G]CGGTGGCTTTCCCCA	4703
rs756043359	snp	A/T	1.7211e-05	0.00293346	intron-variant	NEB	GRCh38.p7	2:151617360	AGATCAACAGTTTAC[A/T]TACATCACTGTAGTT	4703
rs756046096	snp	A/G	1.65894e-05	0.00288	synonymous-codon	NEB	GRCh38.p7	2:151568324	CCCATACCTGGTCCA[A/G]TATCCTAGCAGCCTC	4703
rs756051738	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151728616	GTAGGTGAGAAATTA[C/G]TATTTCTTACAGCAG	4703
rs756052626	snp	C/G	1.68255e-05	0.00290043	intron-variant	NEB, RIF1	GRCh38.p7	2:151503458	TGTAGAAAATAATTA[C/G]AATACCCAGAAAGGT	4703
rs756069640	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151660335	TCCTTTCAGAAACCC[C/T]AAACTGCAAAACATA	4703
rs756070569	in-del	-/AAG			intron-variant	NEB, RIF1	GRCh38.p7	2:151533844	AGAAAGATATATAGT[-/AAG]GAGTTATGTCTTCTT	4703
rs756086092	snp	C/T	3.00838e-05	0.00387827	missense	NEB	GRCh38.p7	2:151691901	TTGATTGCTTCATAT[C/T]CTTGTGTTATTGTCT	4703
rs756093933	snp	A/T	1.83852e-05	0.00303188	intron-variant	NEB	GRCh38.p7	2:151642699	AAAATAGACATTAAT[A/T]GTAAGTTGGATTTAT	4703
rs756098317	snp	A/T	5.17514e-05	0.00508655	missense	NEB	GRCh38.p7	2:151570328	CGGATCTTGTTGTCA[A/T]CCCTGGCTGTGAGGG	4703
rs756101733	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151504906	CCATTGTAGGTAGAT[C/T]GCAGCCTGTACCACT	4703
rs756102340	snp	C/G	1.65611e-05	0.00287755	missense	NEB	GRCh38.p7	2:151694395	GCTGAGGACTCCAAT[C/G]ATTTTCCCTTTGTTT	4703
rs756103485	snp	C/T	1.80801e-05	0.00300661	missense	NEB	GRCh38.p7	2:151684818	TTGGCAAGGTCCACA[C/T]TGATGCTATCAGGGG	4703
rs756106087	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151665321	GGGCGAGGCTGGCAG[A/G]TGAGTCCTTACCTTG	4703
rs756114192	snp	A/G	1.67245e-05	0.00289171	missense, intron-variant	NEB	GRCh38.p7	2:151654038	AGCTGTACAGAAATT[A/G]CATCAACTGGGAGAT	4703
rs756117435	in-del	-/A	1.65594e-05	0.0028774	frameshift-variant, intron-variant	NEB	GRCh38.p7	2:151633784	TTCTTGGCCAGCACC[-/A]CCCCCAGCATGTCCA	4703
rs756123091	snp	A/G	3.32989e-05	0.00408024	missense	NEB	GRCh38.p7	2:151553501	TCATCCTTGTATACA[A/G]TCTAGAGGGTTTTGA	4703
rs756124792	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151548814	TAACACATCCTTTAG[G/T]TGTTAGATTATTAAA	4703
rs756130763	snp	C/T	0.00018238	0.00954761	missense	NEB	GRCh38.p7	2:151656260	TGTTGGTGATGTTGG[C/T]TTGGGCATCCTTTGC	4703
rs756135837	snp	C/T	0.000133236	0.00816089	missense	NEB	GRCh38.p7	2:151677923	GCTCCAGGTCCATGG[C/T]GTCAGGCAAGTAGGT	4703
rs756135944	in-del	-/TAA	1.66418e-05	0.00288455	intron-variant	NEB	GRCh38.p7	2:151643118	ATAAACAAAAAAAAT[-/TAA]TAACCTCCTCAAACA	4703
rs756142785	in-del	-/TT			intron-variant	NEB, RIF1	GRCh38.p7	2:151524005	CCGAGGATGAAACTC[-/TT]AAGGCCTGGGGAGAG	4703
rs756146889	snp	A/T	1.65622e-05	0.00287764	missense, intron-variant	NEB	GRCh38.p7	2:151640024	TGGACACCCAGCCAA[A/T]GCCTCTCATCCACTG	4703
rs756156443	snp	A/G	1.65836e-05	0.0028795	intron-variant	NEB	GRCh38.p7	2:151659034	CAAATCTGCTGGAGA[A/G]AAAGATGACAACAGG	4703
rs756162358	snp	C/T	5.00179e-05	0.00500065	missense	NEB	GRCh38.p7	2:151727860	GTTTCTGATTGCTCA[C/T]AGTCAGATGTCCTTG	4703
rs756174240	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151716363	CAGGCTGGTCTCGAA[C/T]TCCTGACAGGTGATC	4703
rs756175808	snp	A/C	1.68917e-05	0.00290613	intron-variant	NEB	GRCh38.p7	2:151644625	GTTCCCCATAGACAA[A/C]TATAGCATAATGATC	4703
rs756177723	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151577741	ATGCCACCACGCCAG[C/G]CTAATTTTTGTGTTT	4703
rs756185799	snp	C/T	6.62416e-05	0.00575469	missense, intron-variant	NEB	GRCh38.p7	2:151627745	GATCTTGGCCACATG[C/T]ATGGACCACATCATC	4703
rs756190937	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151591897	AGACCCACACAGCTA[C/G]TTATCATTAACTTAA	4703
rs756192566	snp	A/T	0.00220929	0.0331627	missense, intron-variant	NEB	GRCh38.p7	2:151591413	CTGCTCGCAGGTCAT[A/T]ACCAGTCATCTTGAC	4703
rs756196691	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151552408	TGCTATGACACAGGG[A/C]ACAAAAAACACGTTG	4703
rs756196753	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151537408	CTGACCTTTGGTATA[C/T]TGTTTTATAACATAT	4703
rs756204418	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151493161	GCACAGTTAATGTCT[A/G]TTTTAGTGTAAATTT	4703
rs756217803	snp	C/T	3.31934e-05	0.00407377	intron-variant	NEB	GRCh38.p7	2:151697537	GAGTGACAGTAGGAT[C/T]GCTTACATCACTACT	4703
rs756220555	snp	G/T	0.00033173	0.0128746	intron-variant	NEB, RIF1	GRCh38.p7	2:151524655	ACTCAAGAGAGAGGC[G/T]TTTTTTTTTTTTTTT	4703
rs756224064	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151678791	CATGAGGGAAGGTTC[A/G]TGGAAAGTTGGGGCA	4703
rs756238111	snp	C/T	1.65647e-05	0.00287786	synonymous-codon	NEB	GRCh38.p7	2:151674531	GGGAATAGCATCGCC[C/T]AGCACATTGTTGCCC	4703
rs756245968	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151708798	TTCTTCCATAGTCTT[A/C]CCTGTCTCAATAAAG	4703
rs756253354	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151524816	GGGACTGCAGGTGTG[C/T]ACCACCATGCCCGGC	4703
rs756259392	snp	C/T	1.74705e-05	0.00295549	missense	NEB	GRCh38.p7	2:151567420	CTTAGGATCATCTCT[C/T]ATCGTCGGGACACCA	4703
rs756271464	snp	A/C	3.3248e-05	0.00407712	intron-variant	NEB, RIF1	GRCh38.p7	2:151492082	TAATCCCCTCCCCCA[A/C]CCCAGGCTCAGTTAC	4703
rs756281965	snp	A/G	1.70622e-05	0.00292076	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151502846	TCTCTGGAGTGATAG[A/G]TGTTGGGATTCCTTT	4703
rs756284738	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151538831	CAGCTCTGATTCTAA[C/T]CTGAGAATATCATAG	4703
rs756295339	snp	C/T	1.65679e-05	0.00287814	missense, intron-variant	NEB	GRCh38.p7	2:151619573	TCTGACACTTCTTGG[C/T]CAAAACGATACCAAG	4703
rs756307220	snp	C/T	1.66125e-05	0.00288201	intron-variant	NEB	GRCh38.p7	2:151725580	AAAGAATATCAGATA[C/T]TAGCCTAACAAGACA	4703
rs756309002	snp	A/G	2.9546e-05	0.00384345	intron-variant	NEB	GRCh38.p7	2:151630822	CTGTGTATAAACGCT[A/G]TAAAAGAAGATAAGA	4703
rs756314450	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151654226	CTATCTTTAAAGATA[C/T]GGATAAAAATAAAAC	4703
rs756331897	in-del	-/GCCAATG	1.66305e-05	0.00288357	frameshift-variant, intron-variant	NEB	GRCh38.p7	2:151612333	CTCGACCTCTACAGA[-/GCCAATG]GGAACCCATCCTATG	4703
rs756336950	snp	A/T	0.000135597	0.00823287	intron-variant	NEB	GRCh38.p7	2:151570428	CAGATGGGTCACAGC[A/T]TGTCCTCTTGATGCA	4703
rs756338814	snp	G/T	1.66977e-05	0.00288939	intron-variant	NEB	GRCh38.p7	2:151710404	GTCTCCCTCCCAGGA[G/T]GACCAACCAGCCATC	4703
rs756340507	snp	A/C/T	3.35825e-05	0.0040976	intron-variant	NEB	GRCh38.p7	2:151674625	CAGCATCTGTAAGTG[A/C/T]TTCCTCAACTGCTGG	4703
rs756341175	snp	A/C	1.65674e-05	0.00287809	missense, intron-variant	NEB	GRCh38.p7	2:151614365	GGGGATGCTTGTAGT[A/C]TATGTCGCTTACAAG	4703
rs756345641	snp	A/G	4.97096e-05	0.00498521	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151529231	GTTGACTTTGTAGGC[A/G]TCCTTGGCTGCTTTG	4703
rs756348880	snp	A/G	1.69654e-05	0.00291246	intron-variant	NEB	GRCh38.p7	2:151690694	AGCAAAGCACTCTGG[A/G]TCACCCACGCTTGCA	4703
rs756352101	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151705957	GGGAGTAAAGACTAC[A/C]TATTGATCATAGTGT	4703
rs756352186	snp	C/T	1.78905e-05	0.00299081	splice-donor-variant	NEB	GRCh38.p7	2:151553827	TAAGTCACAGGCTTA[C/T]ATCGCTGATCTGATC	4703
rs756355046	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151652812	ATGGGTTCACACAAA[A/G]AGAAATGAGGTACTA	4703
rs756360867	snp	A/C	4.96364e-05	0.00498154	missense	NEB	GRCh38.p7	2:151669108	CTTGTGCTTCAGTTT[A/C]TCTCCCTCTACCTTG	4703
rs756363951	snp	A/G	1.67483e-05	0.00289377	stop-gained, intron-variant	NEB	GRCh38.p7	2:151650864	GGCCAAGTTGCTTTC[A/G]GTAGCCTTGTTTGTA	4703
rs756369116	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151573311	AGTCTTGTTCATATA[A/C]TATCAATGGTAAGGT	4703
rs756383903	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151685184	CAAATCAATGAGAAA[C/T]TGTCTGGGTCACAGC	4703
rs756384471	in-del	-/AGGT	9.18991e-05	0.00677799	frameshift-variant, intron-variant	NEB, RIF1	GRCh38.p7	2:151501442	CATCTCAGGAGTGAC[-/AGGT]AGGGGAGTCCCCTTG	4703
rs756390965	snp	A/C	0.00125214	0.02499	intron-variant	NEB, RIF1	GRCh38.p7	2:151514947	ATGTAAGTAGGAAGG[A/C]AAGACAAGTTAAAAA	4703
rs756396449	snp	C/T	1.65861e-05	0.00287972	missense	NEB	GRCh38.p7	2:151710460	TATCAGCATTCATTC[C/T]GGCATTTGCAACTTC	4703
rs756398214	snp	A/G	3.3145e-05	0.0040708	missense	NEB	GRCh38.p7	2:151656350	TTTTCTTGTACTCCC[A/G]ATCAGATTGCATCTT	4703
rs756403694	snp	A/G	1.65636e-05	0.00287776	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151614483	CTCCCTGTCACTCTG[A/G]ATCTTGGCCACATGG	4703
rs756406274	in-del	-/AGAG			intron-variant	NEB, RIF1	GRCh38.p7	2:151513509	AATAAATCAGATGAC[-/AGAG]GGACACTTTATGTCC	4703
rs756411365	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151638608	GATTTATGAGATCAG[C/G]TCCTTGTCACTGGGA	4703
rs756419543	in-del	-/AGAG	0.0107586	0.0725503	intron-variant	NEB	GRCh38.p7	2:151617488	AAAAAAAAAAAAAAA[-/AGAG]AGAGAGAGAGAGAAA	4703
rs756424328	snp	C/T	1.65809e-05	0.00287926	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151619688	GAGGGACCACATTAT[C/T]TTGGGGTCATCGTGT	4703
rs756424584	snp	C/T			synonymous-codon	NEB	GRCh38.p7	2:151552732	TGTATCTGTGACAAG[C/T]TTGTAGTCATTCCTT	4703
rs756429569	snp	C/T	1.65614e-05	0.00287757	missense, intron-variant	NEB	GRCh38.p7	2:151631169	TGAGAGCATTGTTCT[C/T]GGCCAGCACCTGCTC	4703
rs756435364	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151559930	TGTACCCCAGAACTT[A/G]AAGTATAATAAACCA	4703
rs756436872	snp	A/G	1.66131e-05	0.00288206	intron-variant	NEB, RIF1	GRCh38.p7	2:151490354	GGGACTGCCAAAATC[A/G]GCGCCAGGCACTTGT	4703
rs756460818	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151574304	GTAATTATATTAGCA[A/T]CAATGAGAATCTCAC	4703
rs756461553	snp	G/T	1.65674e-05	0.00287809	synonymous-codon	NEB	GRCh38.p7	2:151576259	GACACTGTCACAAAA[G/T]ATATTCTGGGCGTTT	4703
rs756476348	snp	A/G	9.94398e-05	0.00705053	synonymous-codon	NEB	GRCh38.p7	2:151656297	GACACTGAGCATGTC[A/G]GCAGGGGTGTGGTAG	4703
rs756489221	snp	C/T	1.83781e-05	0.00303129	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151516464	TTTGACTTACCCCAC[C/T]CTGCATCTGCTGAGA	4703
rs756491764	snp	A/T	1.66319e-05	0.00288369	intron-variant	NEB	GRCh38.p7	2:151555047	CCCGATATTTGATCT[A/T]TAGAGAATAAGTAGA	4703
rs756495284	snp	C/T			synonymous-codon	NEB	GRCh38.p7	2:151684802	CAGCGCATATGCCTT[C/T]TTGGCAAGGTCCACA	4703
rs756496204	snp	A/C	1.68258e-05	0.00290045	missense	NEB	GRCh38.p7	2:151541462	CTGACTCTGAAGCTT[A/C]TGCCCTCGCTTGGCT	4703
rs756500097	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151513063	TTTAGTTGGATGCAG[A/G]ATGGGATATGGGTAA	4703
rs756509531	snp	C/G/T	9.28319e-05	0.00681238	intron-variant	NEB	GRCh38.p7	2:151682648	TCTCCCTCTGACACA[C/G/T]CCAGTGGCTTTACCT	4703
rs756512891	snp	C/T	1.65726e-05	0.00287855	missense, intron-variant	NEB	GRCh38.p7	2:151618322	GCACCTGCTCCGGAG[C/T]GTCCGTTATACTGGT	4703
rs756517186	snp	C/T	1.79146e-05	0.00299282	intron-variant	NEB, RIF1	GRCh38.p7	2:151513735	AAGGTACCTAAATGC[C/T]ACTACTAGGTAATAA	4703
rs756517766	snp	C/G	2.13554e-05	0.00326761	intron-variant	NEB	GRCh38.p7	2:151547765	GAAATATCATTACAG[C/G]CATTTAGTAGGGGAC	4703
rs756518712	snp	A/G	1.65748e-05	0.00287874	missense, intron-variant	NEB	GRCh38.p7	2:151609915	ATGTCAGTGACCAAA[A/G]TCTGACATTTCTTGG	4703
rs756520999	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151710968	AAAGAAACAACCACA[A/G]TAAAATTCAACTTGC	4703
rs756526984	snp	C/T	3.31411e-05	0.00407056	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151525175	TACATCACTTTGCTT[C/T]TTGGCCACTTCCATA	4703
rs756529265	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151546645	CTGACTGCAACCTCC[A/G]CCTCCCGAGTTCAAG	4703
rs756535543	snp	A/T	3.51834e-05	0.0041941	intron-variant	NEB	GRCh38.p7	2:151535683	TGGAGCAGTTTATTC[A/T]TACATACCTCATTCA	4703
rs756535708	snp	A/G	1.67091e-05	0.00289038	synonymous-codon	NEB	GRCh38.p7	2:151662162	TTTTGCATTATTCTG[A/G]GCCAAAACCATGTTC	4703
rs756541561	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151668266	ATACTTTTGGAAAAA[C/T]GTTTCTTGTAATGAA	4703
rs756545133	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151625935	CCCAATTAAATAAAA[A/G]GCAAGTATTTCTCAA	4703
rs756558819	snp	C/G	8.5848e-05	0.00655108	intron-variant	NEB, RIF1	GRCh38.p7	2:151493741	TGCCAGGGCTGTTAA[C/G]ATTTTAAGGATTTAT	4703
rs756563857	snp	A/G	5.54483e-05	0.00526508	missense	NEB	GRCh38.p7	2:151664811	ATATCCGGTGTGTCA[A/G]GCATGACATGAATGG	4703
rs756569688	snp	A/G	1.67961e-05	0.00289789	intron-variant	NEB	GRCh38.p7	2:151567510	ATATAAATTCCATCA[A/G]TTTTGACAAGCACAC	4703
rs756590829	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151694488	AGGAAATGTCCCCGA[A/G]GCCAGCCTGTCCAGG	4703
rs756592613	snp	G/T	1.65644e-05	0.00287783	missense, intron-variant	NEB	GRCh38.p7	2:151627084	TTCAGCTTGTCCGGA[G/T]GCTGGCGGTAGATGT	4703
rs756593205	snp	G/T	2.86718e-05	0.00378617	missense	NEB	GRCh38.p7	2:151568685	TCCACAGGCGTAAAG[G/T]TGAGAGTTTCTATTT	4703
rs756597328	snp	A/G	1.66299e-05	0.00288352	synonymous-codon, nc-transcript-variant, intron-variant	NEB, RIF1	GRCh38.p7	2:151506255	CATCCTCTTTATATA[A/G]AACCTGGGCATTCAG	4703
rs756600687	snp	A/G	1.66735e-05	0.00288729	synonymous-codon	NEB	GRCh38.p7	2:151665387	TTCCATTGTGTCCAT[A/G]GCGTAAGTGAACTTC	4703
rs756608986	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151693310	TGTGCAGGATTGTGG[G/T]TTTGTTACATAGGGA	4703
rs756612643	in-del	-/A	1.65905e-05	0.0028801	frameshift-variant, intron-variant	NEB, RIF1	GRCh38.p7	2:151503397	TCAATCTCTGGAGTC[-/A]ACAGTGGTTGGAATG	4703
rs756635997	snp	C/T	6.70916e-05	0.00579148	missense	NEB	GRCh38.p7	2:151677891	ATCACTCTGTATCTG[C/T]ATCATGTTCTTAGAC	4703
rs756639505	snp	C/T	3.31526e-05	0.00407127	missense	NEB	GRCh38.p7	2:151697231	TGCCTCTGTCTTCTT[C/T]GTATTCTGCTTTGTA	4703
rs756646859	snp	G/T	0.00012145	0.00779168	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151526238	AGGTTCCTCTTTCCT[G/T]GACATGTTTCTCTTT	4703
rs756652477	snp	A/C			intron-variant	NEB, RIF1	GRCh38.p7	2:151533145	CTAAGGAATCTATTT[A/C]TTTGAGGCAAATACT	4703
rs756654072	snp	A/T	1.65831e-05	0.00287945	missense, intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151534303	TTCCGCTGCTCATAA[A/T]CAGCTCTGTATTTTT	4703
rs756659726	snp	C/T	1.65641e-05	0.00287781	stop-gained, intron-variant	NEB, RIF1	GRCh38.p7	2:151485829	CACAGTGCCATACAT[C/T]CAGCCTTCATCAATT	4703
rs756671954	in-del	-/AT	6.62987e-05	0.00575717	intron-variant	NEB	GRCh38.p7	2:151563596	CGTGTTAAAGTGGAC[-/AT]TTACTTACCGCACTC	4703
rs756676516	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151712174	AGAGACATGGCCCTA[C/T]CTCTTGCTTGTTGTC	4703
rs756679545	snp	C/T	2.60712e-05	0.00361039	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151490458	GACTTCTCCTCACCC[C/T]CACTGATGCTTAGTG	4703
rs756691673	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151661446	TCTGCAACTGTTTCA[C/T]GTTTAGATCCAAATC	4703
rs756692621	snp	A/G	4.99604e-05	0.00499777	missense	NEB	GRCh38.p7	2:151667857	TTGGGATGGCATCTG[A/G]TCTCAAATCATAGCC	4703
rs756706066	snp	A/C	3.41658e-05	0.00413301	intron-variant	NEB	GRCh38.p7	2:151697143	AGTTCAGACTACAGA[A/C]TTACGTCTTTACACT	4703
rs756711705	snp	C/G	1.67111e-05	0.00289055	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151492438	CATCTCGGGGGTATC[C/G]AATACATAGGCAGCT	4703
rs756715032	snp	C/T	1.6666e-05	0.00288664	intron-variant	NEB	GRCh38.p7	2:151538263	GAAAGAGAAAAAACA[C/T]ATGAATTACAAAAAA	4703
rs756720674	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151487726	GTAAAAGTTTTAGGT[C/T]AAATGGCATGTGTGT	4703
rs756722257	snp	C/T	2.04564e-05	0.00319809	synonymous-codon	NEB	GRCh38.p7	2:151560616	CAGATGCTTCTGGTT[C/T]TTGGCGTGTGTCAGG	4703
rs756723106	snp	A/C	1.65765e-05	0.00287888	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151650323	TTCTGCCTCTAAAGA[A/C]CCCAAGGGACTCCAT	4703
rs756726488	snp	A/T			stop-gained, intron-variant, utr-variant-3-prime	NEB, RIF1	GRCh38.p7	2:151497714	ATGTTTTCTTTGTAT[A/T]ACACCTGTGCGATAA	4703
rs756733221	snp	C/T	0.000370714	0.0136095	intron-variant	NEB	GRCh38.p7	2:151606559	AAATAGTCTCCCTGC[C/T]CGTTTTGTAGAAAAG	4703
rs756738995	snp	C/T	1.65608e-05	0.00287752	missense, intron-variant	NEB	GRCh38.p7	2:151644012	AGTCCTTCTTGTACT[C/T]CCTGTCACTCTGGAT	4703
rs756745218	snp	C/T	4.96783e-05	0.00498364	missense, intron-variant	NEB	GRCh38.p7	2:151640450	TCTTGTAGTCCACAT[C/T]GCTGACTAAGGTCTG	4703
rs756758730	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151511581	AAAGCACAGCTAGGG[C/T]ACGTTAACTATGGCT	4703
rs756763962	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151734051	ACTGCCACTCCTCAG[A/G]CAAATGAAGCCCAGT	4703
rs756765934	snp	A/G/T	5.57091e-05	0.0052775	missense	NEB	GRCh38.p7	2:151547472	CAATGGATCACTTGG[A/G/T]GTGTGTATGGCAGAG	4703
rs756766749	snp	C/T	9.1245e-05	0.00675383	intron-variant, stop-gained, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151498252	TTTCCCCTTTCTTTC[C/T]AAAATACCGAGCTAA	4703
rs756774051	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151672085	AACCCATCAGGAATA[A/C]CCATCTCCTCTTGCT	4703
rs756778687	snp	A/G	1.65872e-05	0.00287981	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151650224	AACTATATCCATGGC[A/G]TCAGGAATGCTGGTG	4703
rs756787775	snp	A/G	4.96923e-05	0.00498434	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151629587	CACGATGGGGATGGC[A/G]TCACTTCGCAAGTCG	4703
rs756790304	snp	C/G			missense	NEB	GRCh38.p7	2:151706957	AGCACATTATAATCT[C/G]CTTTTCCTTTATTCT	4703
rs756804630	snp	A/G	1.65839e-05	0.00287953	missense	NEB	GRCh38.p7	2:151677602	TGTTTTGCCTGGACC[A/G]TAACTGGGGAGTCCA	4703
rs756816194	snp	C/T	1.67276e-05	0.00289197	intron-variant	NEB	GRCh38.p7	2:151656045	AGAAGATAAGCAAAT[C/T]CTACTTTATCTTATC	4703
rs756817624	snp	C/T	1.65888e-05	0.00287996	intron-variant	NEB	GRCh38.p7	2:151694463	TCACACATGCCAGAT[C/T]CCACTCAAGAGGAAA	4703
rs756820051	in-del	-/G			intron-variant	NEB	GRCh38.p7	2:151562921	TCTAGAATAAACTAA[-/G]GTTAATATATACTTT	4703
rs756823337	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151545009	CAAGGCACTATGGGA[A/C]ACATGTAAATAACAT	4703
rs756829657	snp	C/T	2.42163e-05	0.00347959	synonymous-codon	NEB	GRCh38.p7	2:151565809	CCACTCCAGGTCAGC[C/T]CTGTAGACATTCTGA	4703
rs756831276	in-del	-/AAAAAG	5.45033e-05	0.00522003	intron-variant	NEB, RIF1	GRCh38.p7	2:151494283	TGGGTCCAAAAAGCC[-/AAAAAG]AAAAAGAGTTAACAG	4703
rs756840132	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151709426	TATTAATGCTCATAC[A/G]TGGCAAAACATTTTT	4703
rs756846904	snp	G/T			intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151498773	GTATATGGAGACACA[G/T]ACACACAACTCTTCT	4703
rs756852049	snp	A/C	3.49144e-05	0.00417803	missense, intron-variant	NEB	GRCh38.p7	2:151625591	AGGTGTATCAGGCAT[A/C]ATATGGACTTGGGTC	4703
rs756852826	snp	A/T	1.69596e-05	0.00291196	intron-variant	NEB	GRCh38.p7	2:151666407	TATATTTGCACTATT[A/T]GAAAACAAAGGGCAA	4703
rs756856551	in-del	-/TT	0.000191495	0.00978319	splice-acceptor-variant	NEB	GRCh38.p7	2:151733187	GTGGCACCTACAAAC[-/TT]TTCATATTCCATACA	4703
rs756859541	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151624894	TTAGCAAGGCTGAAG[A/G]TAGTTCATAAAAGAA	4703
rs756867494	snp	A/G	1.65993e-05	0.00288086	intron-variant	NEB	GRCh38.p7	2:151552809	ACAAGCCCATGTTGG[A/G]CCATTCCTTATGCTT	4703
rs756871030	snp	A/G	8.27421e-05	0.0064315	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151616092	CTTGGACTCTTCCAA[A/G]GCAAGTTTATAGAGT	4703
rs756875036	snp	G/T	1.6628e-05	0.00288335	missense, intron-variant	NEB	GRCh38.p7	2:151643830	CACATCGCTCTGGAG[G/T]TCATAGGCCTGCCGA	4703
rs756876031	snp	A/G	6.98934e-05	0.00591116	intron-variant	NEB	GRCh38.p7	2:151687763	TTCAGCAAAGGAATG[A/G]TAAGAACAACAGTGT	4703
rs756878272	snp	G/T	8.14631e-05	0.00638161	intron-variant	NEB	GRCh38.p7	2:151707036	AAAGTAACTCTATGG[G/T]TTATTTTTGCCCCCG	4703
rs756896023	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151530380	CTTCTTAAATTTCAG[A/G]GTCGAGGGCCTCGAT	4703
rs756899490	snp	G/T	2.33217e-05	0.00341472	intron-variant	NEB	GRCh38.p7	2:151695707	AGAGAGAACCAATTA[G/T]TTCAGAAGAATTGTT	4703
rs756903450	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151667759	TGGTCTTGAACTCCT[A/G]AAGTCTTTTAGATAG	4703
rs756909344	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151643751	TCAACTCTGCTCACT[A/G]TGGGACTCTGATACT	4703
rs756920047	snp	C/T	1.6755e-05	0.00289435	missense	NEB	GRCh38.p7	2:151695604	TATAGGCATTGACTT[C/T]GTGCTGGATAAAAGC	4703
rs756923494	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151535488	TCTCCCACCACTGAA[C/T]GGTCCCTTCACTTGT	4703
rs756926807	snp	C/T	0.000420442	0.0144929	missense	NEB	GRCh38.p7	2:151658047	TCAGGTCTGAGATCA[C/T]AGCCTTTCTTTTTAG	4703
rs756937043	in-del	-/AA	1.65897e-05	0.00288003	intron-variant	NEB	GRCh38.p7	2:151570048	TCATGGCAAACTGAG[-/AA]AAGAGTTCAACCCCA	4703
rs756946672	snp	A/G	6.60044e-05	0.00574438	intron-variant	NEB	GRCh38.p7	2:151621074	AATTCACATTCACTC[A/G]AAAAGTATATTTTCT	4703
rs756949010	snp	A/T	6.49709e-05	0.00569923	missense	NEB	GRCh38.p7	2:151540431	TTTCATCTTTTCATA[A/T]TGAATCTTGTACTTT	4703
rs756949795	snp	C/T	3.46927e-05	0.00416475	intron-variant	NEB, RIF1	GRCh38.p7	2:151496268	TTTTTTCTTTTCTCG[C/T]CAAGTACCGAGCTAA	4703
rs756951729	snp	C/G	1.69327e-05	0.00290965	intron-variant	NEB, RIF1	GRCh38.p7	2:151503471	TAGAATACCCAGAAA[C/G]GTAAAATGACCGTAA	4703
rs756951979	snp	A/G	3.31466e-05	0.0040709	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151631299	CATAGACCCAATGGG[A/G]ACCCAGCCAATGCCT	4703
rs756954250	snp	C/G	5.88893e-05	0.00542598	intron-variant	NEB	GRCh38.p7	2:151563934	TTTATACAGTATCTA[C/G]AACAAAGAAATACAT	4703
rs756955407	snp	C/G	8.65838e-05	0.00657909	intron-variant	NEB, RIF1	GRCh38.p7	2:151514769	TAATGAGTGTCACTA[C/G]TGCAATTATTTGGAT	4703
rs756955786	snp	A/G	1.6569e-05	0.00287824	intron-variant	NEB	GRCh38.p7	2:151575804	CTGTACTTTGGCTGT[A/G]GAAAGAAACAAAAAT	4703
rs756956766	snp	A/C	6.67401e-05	0.00577629	missense, intron-variant	NEB	GRCh38.p7	2:151643327	GCCAATGCCTTTTAG[A/C]CACTGAAGGTCTGAC	4703
rs756969095	in-del	-/ATAG			intron-variant	NEB, RIF1	GRCh38.p7	2:151500421	TCAGAGTTGTATATA[-/ATAG]ATACACAAATAATTT	4703
rs756969318	snp	A/T	6.63526e-05	0.0057595	intron-variant	NEB	GRCh38.p7	2:151554053	AATCACATGCCAGTT[A/T]TACAGGAAATTGTGC	4703
rs756973168	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151549490	AGCACCCCTCAAAAA[G/T]ATGCTGTCTCTCCTC	4703
rs756975611	snp	A/G	1.65638e-05	0.00287778	intron-variant	NEB, RIF1	GRCh38.p7	2:151524487	CAATGGCTGTTGGGG[A/G]CTGGGGACATTTTCA	4703
rs756979937	snp	A/G	1.68151e-05	0.00289953	intron-variant	NEB	GRCh38.p7	2:151629679	AAGAGTTAAAGCAAA[A/G]GGTTTGACATCAACA	4703
rs756984541	snp	A/G	9.04691e-05	0.00672505	intron-variant, missense	NEB, RIF1	GRCh38.p7	2:151533489	TCAACATATCTGGAC[A/G]CAGAATTTCATTACA	4703
rs756995329	snp	A/G	1.68516e-05	0.00290268	intron-variant	NEB	GRCh38.p7	2:151640337	CCTCTGCACGTTATT[A/G]TGACTCTCAGTACTC	4703
rs756995889	in-del	-/A	8.54664e-05	0.00653651	intron-variant, utr-variant-3-prime	NEB, RIF1	GRCh38.p7	2:151497581	ATCATGAAAGTTTTC[-/A]AAAATCATTAAATAA	4703
rs756999212	snp	C/T	1.6601e-05	0.00288101	missense	NEB	GRCh38.p7	2:151549716	ATCCAGTGGGCAGGG[C/T]GCGCAGGCTGGTTTT	4703
rs757001501	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151644599	AAATGAAGATCATTT[A/T]GGGAAATACTGTTCC	4703
rs757002467	snp	C/T	1.66969e-05	0.00288932	intron-variant	NEB	GRCh38.p7	2:151680680	TTTGAAATACAAATG[C/T]ATTTGTATTAGTTAA	4703
rs757005119	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151551205	AACTCCTGACCTCAG[A/G]TGATCTGCCCGCCTC	4703
rs757006805	snp	G/T	6.62416e-05	0.00575469	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151514362	CTCTTAGCATGTCAG[G/T]TGTATCTTCCATTTC	4703
rs757016884	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151517032	AATGGATAACACATG[A/G]AGCTTTATTTATAAG	4703
rs757027644	snp	C/T	0.000149209	0.00863611	missense, intron-variant	NEB	GRCh38.p7	2:151617380	TCACTGTAGTTTATT[C/T]GGTTGAGTTTGGCTA	4703
rs757028005	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151487177	AGAATTTGAAAACCC[A/G]TAGCACTATTGCATG	4703
rs757045956	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151610271	GCAATGTTTTATACT[G/T]TTTTAAAAATAATTG	4703
rs757051537	snp	A/C	1.6574e-05	0.00287867	synonymous-codon	NEB	GRCh38.p7	2:151554949	GATGTTAAGCTTGCC[A/C]ACTCGGAGGCACCGT	4703
rs757055441	snp	C/T			intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151503179	ATGTTCAAGTATAAT[C/T]GGAAATGTGAGTCAT	4703
rs757057661	snp	C/T	4.1486e-05	0.00455426	intron-variant	NEB	GRCh38.p7	2:151672327	AGAAGTGATCATCCT[C/T]TAAGTGCAAACATCT	4703
rs757070337	snp	A/G	5.02391e-05	0.00501169	synonymous-codon	NEB	GRCh38.p7	2:151671191	AGGGATCCATCCGAT[A/G]CCCTTCAAGAAGCTG	4703
rs757071372	snp	A/G	1.69821e-05	0.00291389	synonymous-codon	NEB	GRCh38.p7	2:151568415	GTCTTTCCGGTATTT[A/G]ATCTAAAAAAAAAAA	4703
rs757082095	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151565324	TATAGATATCTAAAA[A/G]TGAATACAATTCACC	4703
rs757107530	snp	A/G	9.32879e-05	0.006829	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151491761	AACCAGGATTAGTAC[A/G]CCAGACACGTAAACC	4703
rs757108531	snp	A/G	4.97954e-05	0.00498951	missense	NEB	GRCh38.p7	2:151553406	AACTCACATCATCAC[A/G]TAGATCATAAGCATG	4703
rs757122461	snp	C/T	1.65641e-05	0.00287781	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151505493	CGAGCTAATGTGCTT[C/T]TGCGTCTCCTTCACA	4703
rs757122750	snp	C/T	1.65778e-05	0.002879	missense	NEB	GRCh38.p7	2:151568336	CCAGTATCCTAGCAG[C/T]CTCCTGGGCAGTGTG	4703
rs757123029	in-del	-/TTAGA	8.06809e-05	0.0063509	intron-variant	NEB	GRCh38.p7	2:151646270	TTTTCAGTGGTGTTG[-/TTAGA]TTAGTGAATGATACA	4703
rs757137860	in-del	-/T	1.65703e-05	0.00287834	frameshift-variant	NEB	GRCh38.p7	2:151659136	TGATGTGGACTTTGG[-/T]TTTGTCAGCCTCCCA	4703
rs757141482	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151679032	AGAGCAGCAAGAGGA[C/G]ACCCGCAGGAGGAGG	4703
rs757142334	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151726127	AATGTTTTGGGAGTA[C/T]TCTTAAGTGGAGTAG	4703
rs757157808	snp	C/G	3.49901e-05	0.00418256	splice-acceptor-variant, intron-variant	NEB, RIF1	GRCh38.p7	2:151519070	AGCCTTGTATTTAAC[C/G]TGTGTGTTATGGGGG	4703
rs757158172	snp	C/T	1.98742e-05	0.00315225	intron-variant	NEB	GRCh38.p7	2:151679678	CCCAAGCCCACCCAC[C/T]CACATTTTCTAGTTG	4703
rs757163864	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151716527	TTCAGATTGATAGTA[C/T]TCCTATTGGTGAAAT	4703
rs757175445	snp	A/G	2.86324e-05	0.00378357	missense, intron-variant	NEB	GRCh38.p7	2:151610829	GGCATCACGTGGATG[A/G]AGGTTTTGTCAGCAT	4703
rs757176860	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151717735	CATTCATTTCCATGC[C/T]ATGGTTTGCAACTGC	4703
rs757178437	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151656885	GAACATTTCTCTTAA[C/T]GCTGCCCTGAGAAAT	4703
rs757182190	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151712505	TTCTTAATCTTCACA[C/G]ACCACGACATGTTAT	4703
rs757184585	snp	A/G	2.02357e-05	0.0031808	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151496320	CTCGCTCCATCTCGG[A/G]AGTGACAGCTAAAGG	4703
rs757188494	snp	A/G	2.20948e-05	0.00332369	synonymous-codon	NEB	GRCh38.p7	2:151565107	ATCTGGTGAAAACGT[A/G]TATTTGCCCTTTGCT	4703
rs757190749	in-del	-/TTTC			intron-variant	NEB	GRCh38.p7	2:151650956	CTTGCTTTTTTTTCT[-/TTTC]TTTCTTTCTTTTTTT	4703
rs757205373	snp	A/G	1.68337e-05	0.00290114	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151518975	CTTACAGAACTGGCA[A/G]GTTGGCTTGTATTCA	4703
rs757207159	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151618613	TCATTCACTCACTCA[C/T]GCACATTATTGAATC	4703
rs757210732	snp	C/G	1.6896e-05	0.0029065	intron-variant	NEB	GRCh38.p7	2:151546337	GCATTGTGATGATGT[C/G]CACTCACCCAGAGCT	4703
rs757210775	snp	A/C	1.70901e-05	0.00292314	missense	NEB	GRCh38.p7	2:151537212	CAATGCCTTTAAGCC[A/C]AGTCAAGTCTTCTTT	4703
rs757218213	snp	C/T	1.65636e-05	0.00287776	missense	NEB	GRCh38.p7	2:151692099	ATGCAGTGTGTGTGA[C/T]ATGGGTCCTCCATGC	4703
rs757220439	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151705310	ATTATTGTCACTTTT[C/T]TCATTCTGGGTTTTC	4703
rs757230269	snp	A/G	1.98612e-05	0.00315122	intron-variant	NEB	GRCh38.p7	2:151610716	TACGGTGGAAAAAGC[A/G]TTTTAATTAATCTTA	4703
rs757230357	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151538925	GTTCTTTTCTTTTGG[G/T]GTTAACTGAGCAAAC	4703
rs757230955	snp	A/T	1.65696e-05	0.00287828	missense	NEB	GRCh38.p7	2:151697447	TTTAAGTAGGAATCT[A/T]TATATTTTTTCTGCA	4703
rs757232974	snp	A/T	3.42965e-05	0.0041409	intron-variant	NEB	GRCh38.p7	2:151723492	TGTACAGTTTCTAAA[A/T]CAAAAAAGAGTGAAA	4703
rs757234274	snp	A/G	2.10737e-05	0.00324598	intron-variant	NEB	GRCh38.p7	2:151639399	GCTATCAAAAAAAAT[A/G]CACAAATTCATCAGG	4703
rs757238122	snp	C/G	2.53534e-05	0.00356034	intron-variant	NEB	GRCh38.p7	2:151568030	ATCCCTGGGAGCAAG[C/G]TCCCACTTTTGCAAA	4703
rs757248006	snp	A/C	5.39884e-05	0.00519531	missense	NEB	GRCh38.p7	2:151684885	CGTCGCTGGCAATTG[A/C]CTGAGATTTCTTAGC	4703
rs757254996	snp	A/G	1.65836e-05	0.0028795	intron-variant	NEB, RIF1	GRCh38.p7	2:151526122	TGGGGCGTTCTCCCA[A/G]GAGGGAAGCAGAACT	4703
rs757255513	in-del	-/CTT	0.00010463	0.00723215	intron-variant	NEB, RIF1	GRCh38.p7	2:151524654	TACTCAAGAGAGAGG[-/CTT]TTTTTTTTTTTTTTT	4703
rs757263577	snp	A/T	0.000112518	0.00749974	intron-variant	NEB	GRCh38.p7	2:151546034	CAGAAATACAAGTTG[A/T]TTAATCATTTAAGGG	4703
rs757264762	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151705994	TAGGTGATGGGTGCA[C/T]CAAAATCTCAGCAAT	4703
rs757266049	snp	A/G	1.65666e-05	0.00287802	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151644534	AACAGGAAGATCGTA[A/G]CCTTTTCTCTTCAGC	4703
rs757273703	in-del	-/TGGA	0.000431285	0.0146784	intron-variant	NEB, RIF1	GRCh38.p7	2:151529199	GCTTGGGGAAGTTTC[-/TGGA]TGGAACTTACATTGG	4703
rs757273793	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151666554	TAAACAATTAGCAAA[A/C]TATTTTTAATGGCTC	4703
rs757278862	snp	C/T	1.65737e-05	0.00287864	missense	NEB	GRCh38.p7	2:151553910	TCGTGGAGGCGCAGG[C/T]GGTAATCAATCTCAC	4703
rs757285495	snp	A/G	3.32707e-05	0.00407851	intron-variant	NEB	GRCh38.p7	2:151725598	GCCTAACAAGACAGC[A/G]GTGAAAATTTCAGGC	4703
rs757290420	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151507729	TGTCTTTTGTTACAG[A/G]GGTTTTCGCCATGAA	4703
rs757290966	in-del	-/A	1.66615e-05	0.00288626	intron-variant	NEB, RIF1	GRCh38.p7	2:151490080	CATGTTTGTAAGCTG[-/A]AAAAAAAGGGGGCAA	4703
rs757299256	snp	A/G	1.6612e-05	0.00288196	missense	NEB	GRCh38.p7	2:151663711	GGGGTGTGGAAGGAG[A/G]TCTTGGATTTCTCAT	4703
rs757306687	snp	C/T	1.74689e-05	0.00295536	missense	NEB	GRCh38.p7	2:151655335	CAGGCATCACATGAA[C/T]CTTGGTCTTATCTTT	4703
rs757309889	snp	A/C	1.67379e-05	0.00289287	intron-variant	NEB, RIF1	GRCh38.p7	2:151493769	TATTTTTCCTTTCTA[A/C]AATACCGAGCTAAAG	4703
rs757312364	snp	A/T			synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151526212	CTGAGGCGTGTCAGG[A/T]ACGGCATGGCAGGTT	4703
rs757321879	snp	C/G	4.96857e-05	0.00498401	missense, intron-variant	NEB	GRCh38.p7	2:151650725	AACATGTCCACTGGG[C/G]TGGAGAACTTAGTTT	4703
rs757326038	snp	C/T	3.40443e-05	0.00412565	missense	NEB	GRCh38.p7	2:151656460	TAATTGTACTTGTAT[C/T]TATACTGTGAAGAAA	4703
rs757330264	snp	A/T	0.000670705	0.0183003	intron-variant	NEB	GRCh38.p7	2:151570466	CATCGGCTGAAAAAA[A/T]AAAACTGAGAAGTTA	4703
rs757331071	snp	C/T	7.00648e-05	0.0059184	intron-variant	NEB	GRCh38.p7	2:151690710	TCACCCACGCTTGCA[C/T]AAATCAAAGCACTTA	4703
rs757339655	snp	C/T	0.000135358	0.0082256	missense	NEB	GRCh38.p7	2:151675349	GATCAGGACTCATGG[C/T]GTATTTATGTTTCAC	4703
rs757340420	snp	C/T	1.65721e-05	0.0028785	synonymous-codon	NEB	GRCh38.p7	2:151656369	AGATTGCATCTTAGC[C/T]ACTTGCATGGAATGG	4703
rs757351857	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151513267	GAATTCCTGGCATCA[A/G]ATGAGTGGACTGACT	4703
rs757360324	snp	C/G	3.51655e-05	0.00419303	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151502865	TGGGATTCCTTTCCC[C/G]AAATTTTCTTTGTAC	4703
rs757361284	snp	A/G	5.82089e-05	0.00539454	intron-variant	NEB	GRCh38.p7	2:151694636	ATAAAGATTCTGGAC[A/G]AAAAAATTCAGCAAA	4703
rs757391972	snp	A/G	1.6703e-05	0.00288985	intron-variant	NEB	GRCh38.p7	2:151671001	ATTTACGGGCAAATC[A/G]TTTTGAAAGGAAAGC	4703
rs757394301	snp	A/T	1.65633e-05	0.00287774	missense	NEB	GRCh38.p7	2:151563655	ACCACACCAGGGAAT[A/T]CACCGATCACTTTTC	4703
rs757407447	snp	C/T	3.55038e-05	0.00421315	missense	NEB	GRCh38.p7	2:151553830	GTCACAGGCTTACAT[C/T]GCTGATCTGATCTGT	4703
rs757420871	snp	A/G	6.00727e-05	0.00548021	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151493861	CCAGGTTCTCTTTGT[A/G]TAACACCTGTGAGAT	4703
rs757422187	snp	A/T	1.65935e-05	0.00288036	missense	NEB	GRCh38.p7	2:151541540	CTTCTTGCCTGCAGC[A/T]CTGTAGACCAGCTAG	4703
rs757429369	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151673110	TTTTATCAGCAGCTG[C/T]TTTCCAAGCTCACTG	4703
rs757431297	in-del	-/T	1.65855e-05	0.00287967	frameshift-variant, intron-variant	NEB	GRCh38.p7	2:151629641	ATTGGCAAGTTTGTA[-/T]AGAGTCTATGAAAAG	4703
rs757433328	snp	C/T	1.65825e-05	0.00287941	missense	NEB	GRCh38.p7	2:151548319	GTACCTCGCTGGTAA[C/T]ATTGTTGACTCTCCG	4703
rs757438945	snp	A/G	1.65652e-05	0.0028779	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151614495	CTGGATCTTGGCCAC[A/G]TGGATGGACCACATC	4703
rs757444464	snp	C/T	3.7262e-05	0.0043162	intron-variant	NEB	GRCh38.p7	2:151710582	AGCATAACTCATGAA[C/T]TGACAAATAAGACAG	4703
rs757463424	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151654868	TTATGTATTTATTTA[C/T]TAGAGACAGGGTCTC	4703
rs757481415	in-del	-/CTATCAAGAG	1.65636e-05	0.00287776	frameshift-variant, intron-variant	NEB, RIF1	GRCh38.p7	2:151505558	TTGTCCTATTGCTTC[-/CTATCAAGAG]CTTATACTTCACCTG	4703
rs757488944	snp	A/C	2.22225e-05	0.00333328	intron-variant	NEB	GRCh38.p7	2:151682786	TAAAACACCAAGAGA[A/C]AGGTTACATTTCTTT	4703
rs757493228	in-del	-/GAG	0.000781899	0.019757	intron-variant	NEB	GRCh38.p7	2:151617489	AAAAAAAAAAAAAAA[-/GAG]AGAGAGAGAGAGAAA	4703
rs757496436	snp	A/G	1.65627e-05	0.00287769	intron-variant	NEB, RIF1	GRCh38.p7	2:151525915	CAGATTCTACAGTCA[A/G]GTGGCATTGTTGCTG	4703
rs757497327	snp	C/T	1.65605e-05	0.0028775	missense, intron-variant	NEB	GRCh38.p7	2:151640573	TCTGGATCTTGGCCA[C/T]GTGCATGGACCACAT	4703
rs757504190	snp	A/G	1.65351e-05	0.00287528	intron-variant	NEB	GRCh38.p7	2:151665310	GAGGGTTCCCTGGGC[A/G]AGGCTGGCAGGTGAG	4703
rs757505325	snp	A/G	4.17162e-05	0.00456688	missense	NEB	GRCh38.p7	2:151690788	GAATCAGTGACTGCC[A/G]TGAATTTGGTCTTAT	4703
rs757508899	snp	C/T	1.65894e-05	0.00288	missense, intron-variant	NEB	GRCh38.p7	2:151644125	AAGCCTTCCTTGTAC[C/T]TGTACTAGAGAAAAA	4703
rs757517429	snp	A/C	1.65833e-05	0.00287948	intron-variant	NEB	GRCh38.p7	2:151697267	TCTATGAGGAGAAGA[A/C]ATTAGGCATAAGATG	4703
rs757519199	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151514017	ATTACACTTAGGTGC[A/G]CACCACTCCAGTGTA	4703
rs757526825	snp	C/T	1.68117e-05	0.00289923	missense, intron-variant	NEB	GRCh38.p7	2:151650870	GTTGCTTTCGGTAGC[C/T]TTGTTTGTATTTATA	4703
rs757537132	snp	A/T	1.65853e-05	0.00287964	missense	NEB	GRCh38.p7	2:151710465	GCATTCATTCTGGCA[A/T]TTGCAACTTCAAAGC	4703
rs757546480	snp	C/G/T	6.63178e-05	0.00575805	synonymous-codon	NEB	GRCh38.p7	2:151662252	ACTAATAATCTCCAT[C/G/T]GCTTTCTTGTTTTTC	4703
rs757560173	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151732335	AGCCGGTGAGGAAAA[A/T]CCGTAAGATGATAAA	4703
rs757562423	in-del	-/T			intron-variant	NEB	GRCh38.p7	2:151673735	ATTTTTCTTTTTCTT[-/T]TTTTTTTTTTTTTTT	4703
rs757574053	in-del	-/AA			intron-variant	NEB, RIF1	GRCh38.p7	2:151513712	TAGTAGCATTAAAAG[-/AA]AAAAAAAAGGTACCT	4703
rs757579723	snp	A/G	1.65605e-05	0.0028775	missense, intron-variant	NEB	GRCh38.p7	2:151640576	GGATCTTGGCCACGT[A/G]CATGGACCACATCAT	4703
rs757586183	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151675148	TGAAGAGGTAAAGAA[C/G]CATCCTTATGGGATA	4703
rs757590200	snp	C/T	1.65614e-05	0.00287757	synonymous-codon	NEB	GRCh38.p7	2:151535700	ACATACCTCATTCAT[C/T]AATTGAGTTGCATAC	4703
rs757595185	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151628400	GAGATCAAATTTGAC[C/T]GAGGTTTGTTTGGGA	4703
rs757598739	snp	A/T	1.68471e-05	0.00290228	intron-variant	NEB	GRCh38.p7	2:151614596	ACTTGTACTAAAAAA[A/T]TAGAGATATGAGTAT	4703
rs757601764	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151661561	CAGATGTTCAAGGTT[A/G]ATTGTACTTGTTGGT	4703
rs757601781	snp	C/T	3.3151e-05	0.00407117	missense	NEB	GRCh38.p7	2:151569302	GCATGTTTGGCATGA[C/T]TGACGGACACGGAGT	4703
rs757621444	snp	C/T	1.80426e-05	0.00300349	missense	NEB	GRCh38.p7	2:151561071	AGAACTGTTGTGTAT[C/T]TGTCCTTAATCTGAT	4703
rs757621514	snp	C/T	1.65679e-05	0.00287814	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151525194	GCCACTTCCATAGCA[C/T]GTTTCACCTCTGGTG	4703
rs757625697	snp	A/C	2.33713e-05	0.00341835	intron-variant	NEB, RIF1	GRCh38.p7	2:151490543	ATGCAGTTGGGGGAG[A/C]TGTAGCAAACATGAA	4703
rs757629824	snp	C/G	4.17528e-05	0.00456888	intron-variant	NEB	GRCh38.p7	2:151560746	GGGAAAATGCATCTG[C/G]TTAGCTTCTGAGTAG	4703
rs757637316	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151548564	ATTGACAAAATTTCA[A/G]TATTAATCCAGGCCT	4703
rs757638348	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151694761	TTGTCTAGGAAATCA[C/T]GCATATTTTAAATAT	4703

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