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
rs1061305	snp	A/G	0.485063	0.08512	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151490465	GCCAGTGCACTAAGC[A/G]TCAGTGGGGGTGAGG	4703
rs1061317	snp	C/T	0.00358779	0.0422022	utr-variant-3-prime, intron-variant	NEB, RIF1	GRCh38.p7	2:151485548	TATTATTTCTGTGCC[C/T]AGAGTCTTTCTCCAT	4703
rs1061322	snp	A/G	0.000248617	0.0111466	intron-variant, utr-variant-3-prime	NEB, RIF1	GRCh38.p7	2:151497728	TAACACCTGTGCGAT[A/G]AGAAAGCATCCAGAA	4703
rs1063573	snp	C/G	0	0	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151494196	GTCACTCCTGAGATG[C/G]AGAGAGTCAAACGCA	4703
rs2288193	snp	A/T	0.419428	0.183832	intron-variant	NEB, RIF1	GRCh38.p7	2:151492328	ATGATGGTGTGACTA[A/T]ATCCCTTTTTACACA	4703
rs2288194	snp	C/T	0.0221141	0.102801	intron-variant	NEB, RIF1	GRCh38.p7	2:151492333	GGTGTGACTATATCC[C/T]TTTTTACACATTCTG	4703
rs2288195	snp	A/G	0.447267	0.153577	intron-variant	NEB, RIF1	GRCh38.p7	2:151492512	GATGCAGGAGAGACC[A/G]TGAATGAGTGGTGCT	4703
rs2288196	snp	A/G	0.49607	0.0441545	intron-variant	NEB, RIF1	GRCh38.p7	2:151525381	GCTCCCCATTTTGGC[A/G]TCAGTCTGGGACTTA	4703
rs2288197	snp	A/G	0.0926964	0.194308	intron-variant	NEB, RIF1	GRCh38.p7	2:151526345	TCAAACCAGTAGAAC[A/G]GCAGCGTTGACAATA	4703
rs2288198	snp	C/T	0.477175	0.104362	intron-variant	NEB, RIF1	GRCh38.p7	2:151527399	GGTTAACACTCATGA[C/T]AGTGGTTATTATAAA	4703
rs2288199	snp	C/T	0.0106619	0.0722307	intron-variant	NEB	GRCh38.p7	2:151541404	CACATATAATCACCC[C/T]CTGTGATGCCTGAGT	4703
rs2288200	snp	A/T	0.0665968	0.169892	NEB	2	allele_origin=T(germline)/A(germline)	2:151547704	GTTGTATGGATCTTG[A/T]CTTTCAGTTTGTGGT	4703
rs2288201	snp	C/T	0.460677	0.134592	intron-variant	NEB	GRCh38.p7	2:151547780	GCATTTAGTAGGGGA[C/T]GACGAGGGCATCTAC	4703
rs2288202	snp	C/T	0.499996	0.00139776	intron-variant	NEB	GRCh38.p7	2:151549299	AGTGCGTGTGTGAAG[C/T]TGCATTTCCAATAAA	4703
rs2288203	snp	C/T	0.499017	0.0221427	intron-variant	NEB	GRCh38.p7	2:151552902	CACTACTCAACAGAC[C/T]GAGATGCATTTGAAT	4703
rs2288204	snp	A/G	0.00557542	0.0525036	intron-variant	NEB	GRCh38.p7	2:151553089	TATAGCATTGCAAAC[A/G]CTAACAAATCACACT	4703
rs2288205	snp	C/T	0.154993	0.231244	intron-variant	NEB	GRCh38.p7	2:151560418	GCAGAGAGAGACAGG[C/T]AGTGAGCACATAGAC	4703
rs2288206	snp	A/G	0.462495	0.131704	intron-variant	NEB	GRCh38.p7	2:151560550	GGAGAGCAGGGGAGG[A/G]GAGGGAGGGTGGGAA	4703
rs2288207	snp	C/T	0.0267878	0.112589	intron-variant	NEB	GRCh38.p7	2:151562292	TAATTTCCTATCAGC[C/T]GTTGGCTGTGCTTAT	4703
rs2288208	snp	C/T	0.0267878	0.112589	intron-variant	NEB	GRCh38.p7	2:151562404	AATGTCTGAGTCTAT[C/T]GTGAAACCAATTAAA	4703
rs2288209	snp	C/T	0.148996	0.228688	intron-variant	NEB	GRCh38.p7	2:151562524	TGAATACAGGGACAA[C/T]GGGAGCATGGCAGCC	4703
rs2288210	snp	C/G	0.441722	0.160446	missense	NEB	GRCh38.p7	2:151565562	GGATCCACCACACTT[C/G]TAAAGTTAGGATAGT	4703
rs2288211	snp	A/G	0.416342	0.186629	synonymous-codon	NEB	GRCh38.p7	2:151565573	ACTTCTAAAGTTAGG[A/G]TAGTTTTCAAGGGCA	4703
rs2288212	snp	C/T	0.0267878	0.112589	intron-variant	NEB	GRCh38.p7	2:151568002	TGCTATCTCTGCCTT[C/T]GGCATAACTGGAATC	4703
rs2288217	snp	A/G	0.444444	0.157135	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151593174	CAGAACCCTCTGGCA[A/G]CCATCCAATACCCTT	4703
rs3213814	snp	A/G	0.000798403	0.0199641	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151499495	AGACGTCAGACAGAA[A/G]AGACAGATTCAACAA	4703
rs3213815	snp	A/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151499683	TAAGACCACTAAAAT[A/T]CTCAGTGTACAATAG	4703
rs3213816	snp	A/G	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151499694	AAATACTCAGTGTAC[A/G]ATAGAAAAATTGCTT	4703
rs3213817	snp	A/C/T	0.10817	0.208706	intron-variant	NEB, RIF1	GRCh38.p7	2:151503248	ACACACACAGACACA[A/C/T]ACAGAATTGCTGTTA	4703
rs3213818	snp	A/G	0.468249	0.121932	intron-variant	NEB	GRCh38.p7	2:151546197	CACAGATCACATTAA[A/G]GTGATAATCTGCTCA	4703
rs3214502	in-del	-/C	0.328382	0.237395	intron-variant	NEB	GRCh38.p7	2:151560797	TCCTTCTCACACACT[-/C]CCCTACTAACTCCCA	4703
rs3214503	in-del	-/A/AA			intron-variant	NEB	GRCh38.p7	2:151568420	CTAAAAAAAAAAAAA[-/A/AA]TGAGAGGCAAGGGGG	4703
rs3732307	snp	A/G	0.109461	0.206758	intron-variant	NEB, RIF1	GRCh38.p7	2:151495214	TAAATCCTCAACCTC[A/G]GTATCTCCCCTCAGT	4703
rs3732308	snp	C/G	0.342806	0.232136	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151495283	TGAAGAGGAAGAATT[C/G]TGTTGAAATAGTGAT	4703
rs3732309	snp	C/T	0.0103893	0.0713213	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151516460	TTTTTTTGACTTACC[C/T]CACTCTGCATCTGCT	4703
rs3732310	snp	G/T	0.48599	0.0825158	intron-variant	NEB	GRCh38.p7	2:151538020	AAGTCTTACCCAAAG[G/T]TAATGTAAATATGGC	4703
rs3732311	snp	A/G	0.0810805	0.184299	intron-variant	NEB	GRCh38.p7	2:151567091	AAATTTCAAGCACTT[A/G]TGGATCTGGGATGTT	4703
rs3732312	snp	C/T	0.347473	0.230215	intron-variant	NEB	GRCh38.p7	2:151569178	TTGAAATGGTTAAGA[C/T]TGCTGATATTAGATG	4703
rs3771900	snp	A/G	0.461813	0.132798	intron-variant	NEB, RIF1	GRCh38.p7	2:151492880	TATTTTCCTTAGGTT[A/G]TGTCCAGACTTCATA	4703
rs3771901	snp	A/G	0.334642	0.235236	intron-variant	NEB	GRCh38.p7	2:151575967	TTTGATATAAAATCT[A/G]TATTATTCCCTTTTA	4703
rs3815852	snp	C/G	0.493793	0.055364	intron-variant	NEB, RIF1	GRCh38.p7	2:151505884	TAGGATAAACAGATT[C/G]ACATACATATATCCA	4703
rs3815853	snp	A/G			synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151579338	GGGCGACACACTTAC[A/G]TCGCTCTGTAGGTCG	4703
rs3821324	snp	A/G	0.00979356	0.0692883	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151485796	GGCTGGGAGCATTCC[A/G]GTCCTGCCAGTCCTC	4703
rs3832166	in-del	-/CGTGCTAATG			intron-variant	NEB, RIF1	GRCh38.p7	2:151495460	TGATGCGTGCTAATG[-/CGTGCTAATG]TTTTAGAAGCACTGT	4703
rs3835058	in-del	-/T	0.46845	0.121572	intron-variant	NEB, RIF1	GRCh38.p7	2:151503623	CCAAAATAGTAAAAA[-/T]TTTTACTACTTTGAA	4703
rs4130862	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151609668	TACCATTCACATTGT[G/T]TAATATAAAATCCAT	4703
rs4233649	snp	A/G	0.466721	0.124627	intron-variant	NEB, RIF1	GRCh38.p7	2:151502229	TGCAGGAAAGAGTGG[A/G]AGTGAGGCGAGGGAA	4703
rs4233650	snp	A/G	0.477853	0.102875	intron-variant	NEB, RIF1	GRCh38.p7	2:151529676	CCTGGGACCACAGGC[A/G]TGCGCCACCTCACCC	4703
rs4233651	snp	A/C	0.4711	0.116682	intron-variant	NEB, RIF1	GRCh38.p7	2:151529878	AAAGGACCAGTTGGA[A/C]CCCTATTCATTCAGG	4703
rs4233652	snp	C/T	0.499563	0.0147699	intron-variant	NEB	GRCh38.p7	2:151550713	CACCATCACAGTTCA[C/T]TGCATCCTTGACCTC	4703
rs4233653	snp	C/T	0.350982	0.228698	intron-variant	NEB	GRCh38.p7	2:151631060	GACCCCACGCCTTCA[C/T]AGATAATTTAGACTC	4703
rs4248068	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151591172	AGAGTTGCAGAACCA[A/G]ACATAGATGCAAAAG	4703
rs4266011	snp	C/T	0.376791	0.215463	intron-variant	NEB	GRCh38.p7	2:151717850	GACCATATACCTCCT[C/T]TGTTCTTTTTTTTTT	4703
rs4271765	snp	C/T	0.495016	0.0496707	intron-variant	NEB	GRCh38.p7	2:151692826	AATACAAAAATTAGC[C/T]GGGCGTGATGGCACA	4703
rs4289189	snp	C/T	0.49533	0.0480965	intron-variant	NEB	GRCh38.p7	2:151682963	TTTCCTTCTAACTGG[C/T]GTTATGTTCCATTTC	4703
rs4300824	snp	C/T	0.44755	0.153212	intron-variant	NEB	GRCh38.p7	2:151725352	ACTAGCTCATAGTAA[C/T]TCAACTGCTCATTCT	4703
rs4303716	snp	A/G	0.315913	0.241154	intron-variant	NEB	GRCh38.p7	2:151617487	CAAAAAAAAAAAAAA[A/G]AGAGAGAGAGAGAGA	4703
rs4316939	snp	C/T	0.404559	0.196498	intron-variant	NEB	GRCh38.p7	2:151668606	ATTAGATGTCTAGAC[C/T]ACTCAAGAGAAAGGC	4703
rs4327235	snp	A/G	0.00793638	0.0624916	missense	NEB	GRCh38.p7	2:151567409	AACCAAACCAGCTTA[A/G]GATCATCTCTCATCG	4703
rs4338956	snp	C/T	0.0271762	0.113356	intron-variant	NEB, RIF1	GRCh38.p7	2:151522771	ATTTTCTTAAGATGC[C/T]TCATCATAGGGGTGT	4703
rs4358117	snp	C/T	0.493703	0.0557558	intron-variant	NEB	GRCh38.p7	2:151717946	GCAAGCTCCGCCTCC[C/T]GGGTTCAGGCCATTC	4703
rs4364020	snp	A/G/T	0.0890224	0.191284	intron-variant	NEB	GRCh38.p7	2:151561167	AATACATAAAGACAA[A/G/T]AAATAGTTTGTCCCT	4703
rs4372897	snp	C/T	0.499992	0.00199679	intron-variant	NEB	GRCh38.p7	2:151550853	gtttcaccatgttgc[C/T]caggctggtcttgaa	4703
rs4374369	snp	C/T	0.497613	0.0344622	intron-variant	NEB	GRCh38.p7	2:151713465	ATGTGATGGAAGAAT[C/T]TCCATGGTTTTAGAG	4703
rs4375863	snp	A/G	0.490398	0.0686206	intron-variant	NEB	GRCh38.p7	2:151717885	TTGAGACGGAGTCTC[A/G]CTATGTTGCCCAGGC	4703
rs4378803	snp	A/G	0.00358779	0.0422022	intron-variant	NEB	GRCh38.p7	2:151645849	CTCTGCCTGCAAAGA[A/G]TGCCTGTCCACACTG	4703
rs4381780	snp	C/G	0.0517044	0.152246	intron-variant	NEB	GRCh38.p7	2:151704766	CCACTGTCTGGCACT[C/G]CCTAGTGAGATGAAC	4703
rs4381781	snp	C/G	0.496778	0.0400063	intron-variant	NEB	GRCh38.p7	2:151705086	AACCTTCATGAAAAA[C/G]TTATATAAGGTGAGA	4703
rs4384787	snp	A/C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151511387	TGTAATTTTACAATA[A/C/T]ACAACTATATGTTTC	4703
rs4410290	snp	C/T	0.0185938	0.0946107	intron-variant	NEB	GRCh38.p7	2:151704516	caatcagcgagactc[C/T]gtgggcgtaggaccc	4703
rs4413159	snp	A/G	0.490398	0.0686206	intron-variant	NEB	GRCh38.p7	2:151717770	ATTCTCTTAACCAGC[A/G]TCTTCAACTCCCAAC	4703
rs4414676	snp	C/T	0.085037	0.187849	intron-variant	NEB, RIF1	GRCh38.p7	2:151491671	GTTGTAAGCCTTTTT[C/T]AGCTAACACACCATT	4703
rs4425075	snp	A/G	0.49621	0.0433651	intron-variant	NEB	GRCh38.p7	2:151733507	CCAAACACTTAGAGA[A/G]AAGACATTTTCCAGC	4703
rs4453694	snp	C/T	0.371785	0.218331	intron-variant	NEB	GRCh38.p7	2:151683036	CCAACCTGGAAAATG[C/T]TCGAGTCAAAGCTGC	4703
rs4461258	snp	C/T	0.333722	0.235565	intron-variant	NEB	GRCh38.p7	2:151573165	AGTAATGGTGATACA[C/T]TTGTAAAGAAAATGC	4703
rs4464268	snp	G/T	0.375399	0.216275	intron-variant	NEB	GRCh38.p7	2:151702594	gttagctcttcttgt[G/T]gaattgatcccttta	4703
rs4465763	snp	A/G	0.453939	0.144598	intron-variant	NEB	GRCh38.p7	2:151683399	TAAAATGCTACTCTT[A/G]TTGTCTGACCATAGG	4703
rs4484033	snp	A/G	0.0513262	0.151752	intron-variant	NEB	GRCh38.p7	2:151687098	ATCATTTTAAAAATT[A/G]TTTTTCAATTAGAAG	4703
rs4503987	snp	A/C	0.172351	0.237636	intron-variant	NEB	GRCh38.p7	2:151684322	GATCTGCAGAAAAAA[A/C]CGTTATAAATATTTA	4703
rs4507102	snp	A/T	0.342134	0.232404	intron-variant	NEB	GRCh38.p7	2:151632163	TCACTTTATTAAAAA[A/T]TTTTTTTTTGCTGAA	4703
rs4536649	snp	C/T	0.469937	0.118861	intron-variant	NEB	GRCh38.p7	2:151658239	GAATGTTCTTACAAG[C/T]AACATAACTGTGTTT	4703
rs4544436	snp	A/C/G	0.023584	0.106003	NEB	2	allele_origin=G(germline)/A(germline)	2:151561322	TTGTAGCTGTGAAGA[A/C/G]AAACAAAAGTCATCA	4703
rs4564765	snp	C/G	0.499866	0.0081858	intron-variant	NEB	GRCh38.p7	2:151641134	GCCTGCAAAGAATGT[C/G]TGTATATTTATACAC	4703
rs4564766	snp	A/T	0.490673	0.0676508	intron-variant	NEB	GRCh38.p7	2:151695828	CATCTGCATTACTGA[A/T]CCTGTGTGCAGGACA	4703
rs4575719	snp	A/C	0.499942	0.00539106	intron-variant	NEB	GRCh38.p7	2:151553295	AGCTCAGCCACCCCC[A/C]AGAGCTGGCCTGTGA	4703
rs4599105	snp	A/G	0.471292	0.116318	intron-variant	NEB	GRCh38.p7	2:151625332	TTTTTGTGTCTGTCT[A/G]TCTATCTGTCTGTCT	4703
rs4602223	snp	A/G	0.0441095	0.141807	intron-variant	NEB, RIF1	GRCh38.p7	2:151486036	ACTCCACAAACTTAA[A/G]TTGAACAAAAGAGAA	4703
rs4605369	snp	C/T	0.0123036	0.0774623	intron-variant	NEB	GRCh38.p7	2:151561974	CTAGAAGAGCTTTGA[C/T]TGGGAGAGGAGGGGC	4703
rs4611637	snp	A/G	0.381169	0.212826	synonymous-codon	NEB	GRCh38.p7	2:151717467	TATATCTGGAGGATC[A/G]GCCAGAGGCGTGAAT	4703
rs4616478	snp	C/T	0.192715	0.243348	intron-variant	NEB	GRCh38.p7	2:151578307	ACAAGTGGTCTGGAG[C/T]GTGCTGCTAACTTTT	4703
rs4625904	snp	C/T	0.497211	0.037236	upstream-variant-2KB	NEB	GRCh38.p7	2:151736357	TGCACATTTTGAAAA[C/T]TGATAGATATTGTCA	4703
rs4641933	snp	A/G	0.00478085	0.0486577	intron-variant	NEB, RIF1	GRCh38.p7	2:151500870	TCCCAAAGTGCTGAG[A/G]TGACAGGTGTGAGCC	4703
rs4643540	snp	A/G	0.498459	0.0277128	intron-variant	NEB, RIF1	GRCh38.p7	2:151504053	AGTCCATATTTTTTA[A/G]TAGTAGTATCTAAGG	4703
rs4664055	snp	A/C	0.46754	0.123192	intron-variant	NEB	GRCh38.p7	2:151545657	AGACATAGGAAGAGC[A/C]AGTATGAATATGCGT	4703
rs4664056	snp	C/G	0.498982	0.0225409	intron-variant	NEB	GRCh38.p7	2:151552459	TACTTCATAGACTCG[C/G]ATCACCTACAACTCC	4703
rs4664057	snp	A/G	0.416545	0.186448	intron-variant	NEB	GRCh38.p7	2:151555429	TACTAAAAGGAGTGC[A/G]AGATTAAAACTGTGC	4703
rs4664058	snp	C/T	0.329084	0.237162	intron-variant	NEB	GRCh38.p7	2:151555689	TCTTCCAAAACTCAG[C/T]GATTTGCACCTCTGT	4703
rs4664059	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151608935	AAAAAAAAAAAAAAG[G/T]TAAATGTCAACATTT	4703
rs4664060	snp	A/T	0.389152	0.207694	intron-variant	NEB	GRCh38.p7	2:151608962	ATTTAATGAAAAAAT[A/T]GGCAAAGATTGTATG	4703
rs4664061	snp	A/G	0.296364	0.245663	intron-variant	NEB	GRCh38.p7	2:151608981	AAAGATTGTATGAGA[A/G]GCAAGGTGCAGGCCT	4703
rs4664062	snp	C/T	0.293807	0.246132	intron-variant	NEB	GRCh38.p7	2:151608995	AAGCAAGGTGCAGGC[C/T]TTCAGCACTGAAACT	4703
rs4664063	snp	A/G	0.0410537	0.137264	intron-variant	NEB	GRCh38.p7	2:151609095	TTGTGATCATAAGTT[A/G]AAGTCGTGAGTGCTA	4703
rs4664064	snp	C/G	0.489259	0.0724914	intron-variant	NEB	GRCh38.p7	2:151609291	GACGGGATAAGTGCA[C/G]GAGATTGTACTTCCA	4703
rs4664065	snp	C/T	0.469148	0.120308	intron-variant	NEB	GRCh38.p7	2:151625947	AAAAGCAAGTATTTC[C/T]CAAGCATATATTCAC	4703
rs4664455	snp	C/T	0.46014	0.13543	intron-variant	NEB, RIF1	GRCh38.p7	2:151493948	AGTTGGGGGGAAATG[C/T]TATGTTTAATCTATT	4703
rs4664475	snp	C/T	0.486218	0.0818596	synonymous-codon, intron-variant	NEB, RIF1	GRCh38.p7	2:151531039	ATGCAGCAACATGGG[C/T]GTGTCGTGGATTGTG	4703
rs4664485	snp	A/G	0.498009	0.0314867	intron-variant	NEB	GRCh38.p7	2:151545165	ATGGGCAGCAGAGCA[A/G]GGAGCCACTGAAGAC	4703
rs4664486	snp	C/T	0.498813	0.0243321	intron-variant	NEB	GRCh38.p7	2:151546500	GTAAGTCAGGAAACA[C/T]AAAAGATGGAGTAGC	4703
rs4664487	snp	C/G	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151606491	AGAAAGCTTCTAGCA[C/G]AGGATGAGATGCAAT	4703
rs4664489	snp	C/T	0.270654	0.249145	intron-variant	NEB	GRCh38.p7	2:151607640	AATAGGGAATCAATA[C/T]CTGAAACATTAAGCC	4703
rs4664490	snp	C/G	0.362523	0.223246	intron-variant	NEB	GRCh38.p7	2:151615409	CTTAGGAGGTGTTTC[C/G]CATGTGAAGAAAAGG	4703
rs4664491	snp	C/T	0.340784	0.232934	intron-variant	NEB	GRCh38.p7	2:151623472	ACTTCATTTTTATAC[C/T]CCATTCTCAAATTAG	4703
rs4664492	snp	A/C	0.318656	0.240388	intron-variant	NEB	GRCh38.p7	2:151630268	TGTTGATAGAGAACA[A/C]TTCTTCCTTATGCCT	4703
rs4664493	snp	A/G	0.477515	0.103619	intron-variant	NEB	GRCh38.p7	2:151635810	TCAATAGCAAGCACC[A/G]CATGTGTTTTAAAAT	4703
rs4664494	snp	C/T	0.482905	0.0908579	intron-variant	NEB	GRCh38.p7	2:151643066	CAAAGGAATCAAAAA[C/T]AAGTTTTCTTTTATA	4703
rs4664496	snp	C/T	0.291083	0.246609	intron-variant	NEB	GRCh38.p7	2:151666042	GTGGCTCCTGTTTTT[C/T]CCTCCCACCCATTAG	4703
rs4664497	snp	G/T	0.468148	0.122112	intron-variant	NEB	GRCh38.p7	2:151685778	CTTTGACAGAAAAAT[G/T]TTGACCCACTGCCTT	4703
rs4664498	snp	A/G	0.412583	0.189912	intron-variant	NEB	GRCh38.p7	2:151718903	TTCCAACAATGCAGA[A/G]CTATTCATAGATCCC	4703
rs4664499	snp	A/C	0.376791	0.215463	intron-variant	NEB	GRCh38.p7	2:151727639	AGAGTGAGTTGAGAT[A/C]AGTAATTTCTTAATA	4703
rs4664500	snp	G/T	0.00358779	0.0422022	intron-variant	NEB	GRCh38.p7	2:151728878	AATAGGTTGTTTTCT[G/T]CCCATGATTACCTAG	4703
rs4664501	snp	C/T	0.489318	0.0722982	intron-variant	NEB	GRCh38.p7	2:151729163	ATTTCAATGCATCAT[C/T]AGGGACGAAGCCCTG	4703
rs4994327	snp	C/T	0.460252	0.135255	intron-variant	NEB, RIF1	GRCh38.p7	2:151494612	AGAAGGTTGAGGCTG[C/T]TCCTAATACATCAGC	4703
rs5005569	snp	C/G	0.440884	0.161442	intron-variant	NEB	GRCh38.p7	2:151664036	ATTTTTTTTTTTCCC[C/G]AGACTTGAGTCCATG	4703
rs5835368	in-del	-/T			frameshift-variant, intron-variant	NEB, RIF1	GRCh38.p7	2:151491723	TGGATGTTGTCTTCT[-/T]GCTGGATCATAGTCA	4703
rs5835369	in-del	-/A	0.470424	0.117954	intron-variant	NEB, RIF1	GRCh38.p7	2:151520040	TTTCTAATGCAAAAC[-/A]AAAAAAAAAAAAAAT	4703
rs5835371	in-del	-/T	0.5	0	intron-variant	NEB, RIF1	GRCh38.p7	2:151524655	ACTCAAGAGAGAGGC[-/T]TTTTTTTTTTTTTTT	4703
rs5835372	in-del	-/T	0.461923	0.132621	intron-variant	NEB, RIF1	GRCh38.p7	2:151532747	GAAAGCTCAATTAAC[-/T]TTTTTTTTTTGGTCT	4703
rs5835373	in-del	-/ATT/ATTATT/ATTATTATTATT/ATTATTATTATTATTATT	0.413416	0.189196	intron-variant	NEB	GRCh38.p7	2:151550947	ATTATTATTATTATT[lengthTooLong]TGAAACGGAGTTTTG	4703
rs5835375	in-del	-/T	0	0	intron-variant	NEB	GRCh38.p7	2:151664022	ACTCTTTTTACTTCA[-/T]TTTTTTTTTTCCCGA	4703
rs5835376	in-del	-/T	0.0894459	0.191631	intron-variant	NEB	GRCh38.p7	2:151680373	TTTGATTATATATGA[-/T]TTTTTTTTTTTTTGC	4703
rs5835379	in-del	-/TT/TTT/TTTT	0.498369	0.0285077	intron-variant	NEB	GRCh38.p7	2:151717855	ATACCTCCTCTGTTC[-/TT/TTT/TTTT]TTTTTTTTTTTTTTT	4703
rs6414089	snp	A/G	0.496681	0.0405994	intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151534663	ACAGCTTTACCAACT[A/G]AGGCTGTGAGAATCT	4703
rs6414090	snp	C/T	0.0685596	0.171987	intron-variant	NEB	GRCh38.p7	2:151534745	AATGCTATTAATTTA[C/T]TGGATTATAAAGGAG	4703
rs6433469	snp	A/G	0.497241	0.037038	intron-variant	NEB, RIF1	GRCh38.p7	2:151509570	ggactgctatttctc[A/G]tggcccaataatgaa	4703
rs6433481	snp	C/T	0.478768	0.100824	intron-variant	NEB, RIF1	GRCh38.p7	2:151531248	GCTCTCTGCTAAGAC[C/T]TCAGTGTTTCCAGCT	4703
rs6433482	snp	C/T	0.462691	0.131387	intron-variant	NEB, RIF1	GRCh38.p7	2:151533028	TAATCCTCATCTCCC[C/T]GCAACAGTTGTAGTG	4703
rs6433504	snp	A/G	0.216048	0.247684	intron-variant	NEB	GRCh38.p7	2:151564843	AGCCCGGCACATCAC[A/G]GGAGCTCAAAAGCAC	4703
rs6433566	snp	C/T	0.466824	0.124448	intron-variant	NEB	GRCh38.p7	2:151684563	ACTTAGCAAGGTTGA[C/T]ATATTTCCCAGAGGG	4703
rs6433569	snp	A/C	0.397607	0.201798	intron-variant	NEB	GRCh38.p7	2:151695548	ACAGGTTGTCAGTAC[A/C]TCACATGGTACAGGG	4703
rs6433575	snp	A/G	0.494976	0.0498674	intron-variant	NEB	GRCh38.p7	2:151711394	AATGGGTCTCAAGGC[A/G]CTGGCATATGCCTAC	4703
rs6433576	snp	C/T	0.0341408	0.126114	intron-variant	NEB	GRCh38.p7	2:151713441	ATCAATGGAAATCTT[C/T]CCAATTCTATGTGAT	4703
rs6433579	snp	C/T	0.0341408	0.126114	intron-variant	NEB	GRCh38.p7	2:151714956	AGCATTTCTCCCTAA[C/T]ACAACTATTATTTTG	4703
rs6433584	snp	A/C	0	0	intron-variant	NEB	GRCh38.p7	2:151720323	AATCTATGTGCCTAC[A/C]CATGGTGCATTCTGC	4703
rs6433590	snp	A/C	0.375996	0.215928	intron-variant	NEB	GRCh38.p7	2:151731606	ACCTGCTGGTCAGAC[A/C]CAGATGCTGTAATGG	4703
rs6704618	snp	A/T	0.49931	0.0185575	intron-variant	NEB	GRCh38.p7	2:151536540	AGCTAGCATGCCACC[A/T]GTTTTTAAACAGCTT	4703
rs6705355	snp	A/T	0.109461	0.206758	intron-variant	NEB	GRCh38.p7	2:151537313	ATCTATACAAGTGGA[A/T]CAAACAGAAGCACTA	4703
rs6709752	snp	C/T	0.000629754	0.0177336	synonymous-codon	NEB	GRCh38.p7	2:151672447	GTAATGATGCAATGG[C/T]TGTTTGTAGTTGACA	4703
rs6709886	snp	A/G	0.462949	0.131056	synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151633705	GACATCGCTCTGGTC[A/G]GGCAGGCATGTCCAC	4703
rs6710212	snp	A/G	0.014256	0.0832151	missense, intron-variant	NEB	GRCh38.p7	2:151633944	GGCCAAGTTGCTTGC[A/G]GTAACCATCTTTATA	4703
rs6711382	snp	A/G	0.286811	0.247275	missense	NEB	GRCh38.p7	2:151674563	TGGCTATTAAGTCAT[A/G]CCAATCCCGTTTATA	4703
rs6712443	snp	A/G	0.440884	0.161442	intron-variant	NEB	GRCh38.p7	2:151669535	AGAGGTAACATTTAC[A/G]CTCAAACTTGGAGAG	4703
rs6712533	snp	A/G	0.440609	0.161766	intron-variant	NEB	GRCh38.p7	2:151669568	Gggcagaggaagagc[A/G]ttcgggacctgaggc	4703
rs6713162	snp	A/G	0.37898	0.214159	NEB	2	allele_origin=G(germline)/A(germline)	2:151640012	CCAAAGAGCCAATGG[A/G]CACCCAGCCAATGCC	4703
rs6715755	snp	C/T	0.495855	0.045338	intron-variant	NEB	GRCh38.p7	2:151719488	ATATCTACCTAGTGC[C/T]TATAACAAAAGCTTT	4703
rs6716286	snp	C/T	0.469445	0.119766	intron-variant	NEB	GRCh38.p7	2:151719922	ACAAACTGAAGACTT[C/T]ATTTTAGGCATAGGA	4703
rs6717213	snp	C/T	0.112397	0.208723	NEB	2	allele_origin=T(germline)/C(germline)	2:151619616	GCTGCTGTACCTTGT[C/T]TTGTATTTCTCAAAA	4703
rs6718372	snp	C/G	0.4444	0.15719	intron-variant	NEB, RIF1	GRCh38.p7	2:151489357	ATTAATAGGGGAGAT[C/G]TAAGATAAGGCATGT	4703
rs6718653	snp	A/C	0.430136	0.173352	intron-variant	NEB, RIF1	GRCh38.p7	2:151489604	GTCTCACTATGTTGC[A/C]TAGGCTGGTCTCAAA	4703
rs6718654	snp	A/C/T	7.96464e-05	0.00631006	intron-variant	NEB	GRCh38.p7	2:151549775	CAGGTTAAATGACAT[A/C/T]GGGCATCAAGTAACT	4703
rs6719297	snp	A/G	0.476746	0.10529	intron-variant	NEB, RIF1	GRCh38.p7	2:151507685	TCTGAAGCTTTTATT[A/G]AATAAATTGTGTGTC	4703
rs6720169	snp	A/C	0.497959	0.0318836	intron-variant	NEB	GRCh38.p7	2:151616892	CGGACAATGATTCAT[A/C]TATGGACCTGGGATT	4703
rs6721666	snp	C/G	0.482245	0.092629	intron-variant	NEB, RIF1	GRCh38.p7	2:151525940	TTGCTGCCAAGAGAC[C/G]GGTGGTTGATCACTT	4703
rs6723129	snp	C/T	0.497211	0.037236	intron-variant	NEB	GRCh38.p7	2:151726882	AAATAATTAGGAGAT[C/T]CTACAATTTTTTTTT	4703
rs6723316	snp	C/T	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151712130	TACACATACCTCAGG[C/T]TAGGATCTCCTAATG	4703
rs6724796	snp	C/T	0.419776	0.18351	intron-variant	NEB	GRCh38.p7	2:151556299	gaaattatcagagtg[C/T]actgtctctagtcta	4703
rs6725513	snp	C/T	0.462363	0.131916	intron-variant	NEB	GRCh38.p7	2:151541889	TTCCCAATCCCCTCT[C/T]TTCACCTGCAAACAG	4703
rs6730454	snp	C/T	0.497613	0.0344622	intron-variant	NEB, RIF1	GRCh38.p7	2:151522440	TTGTTTTCATTTCAT[C/T]ATTTAACTTGATCAG	4703
rs6730589	snp	A/C	0.489201	0.0726845	intron-variant	NEB	GRCh38.p7	2:151719493	TACCTAGTGCCTATA[A/C]CAAAAGCTTTCATGG	4703
rs6731486	snp	A/G	0.418974	0.184249	intron-variant	NEB	GRCh38.p7	2:151554218	TATAGCTGAAATAAT[A/G]TGTAGCTTCTTTACA	4703
rs6732307	snp	C/T	0.469937	0.118861	intron-variant	NEB	GRCh38.p7	2:151613704	cccccttgctgttct[C/T]gtgatagtgagtgaa	4703
rs6733688	snp	A/C	0.0236746	0.106192	intron-variant	NEB, RIF1	GRCh38.p7	2:151489887	GTTTGGTTAAAAAAA[A/C]CCGTAATACCTAATA	4703
rs6733707	snp	C/T	0.416871	0.186156	intron-variant	NEB	GRCh38.p7	2:151558881	atacctttcaggaca[C/T]aggcatgggcaaaca	4703
rs6733811	snp	C/T	0.499741	0.0113788	intron-variant	NEB	GRCh38.p7	2:151689631	AGCCAAAGGCAAAAA[C/T]GCACAAGATTGAGAA	4703
rs6733909	snp	C/T	0.497445	0.0356514	intron-variant	NEB	GRCh38.p7	2:151689684	GCAGAGTCCATTGCC[C/T]ACCTAAGCCAATAAG	4703
rs6734148	snp	A/T	0.495252	0.0484902	intron-variant	NEB	GRCh38.p7	2:151719947	ATAGGACAACAGGAT[A/T]TTTCATGGCTGGTTA	4703
rs6735208	snp	A/T	0.375058	0.216473	missense	NEB	GRCh38.p7	2:151679984	TGGTGGCAGGTTGTA[A/T]TTGTGAATAATTTCC	4703
rs6735678	snp	A/G	0.462582	0.131564	intron-variant	NEB	GRCh38.p7	2:151542058	CACCTACCCACATCA[A/G]TGAAGTCACACTCAT	4703
rs6736236	snp	C/T	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151695319	GCAATTAAGCATACA[C/T]GAGACGTAGCATTCT	4703
rs6739271	snp	A/T	0.161596	0.233848	intron-variant	NEB	GRCh38.p7	2:151555923	TTTCCTAAAATAAGG[A/T]CAGAATACTTCTTTT	4703
rs6741567	snp	C/T	0.374	0.217081	intron-variant	NEB	GRCh38.p7	2:151721500	CACCACCCATGCCCT[C/T]GGGACCACCACCTCC	4703
rs6744470	snp	C/T	0.496874	0.0394129	intron-variant	NEB	GRCh38.p7	2:151536782	ACTAGGTGGTTTGCC[C/T]CACGTCATACATTAT	4703
rs6745072	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151698203	TCCAAACTCAAAAAA[A/T]TTTTTTTTCTTTCTT	4703
rs6747113	snp	C/G	0.496937	0.0390173	intron-variant	NEB	GRCh38.p7	2:151702732	ttggtagatcttcca[C/G]catccttttattttg	4703
rs6749823	snp	C/T	0.373397	0.217424	intron-variant	NEB	GRCh38.p7	2:151708541	ggaaggaccccagag[C/T]tcagcccctaaagtt	4703
rs6750147	snp	A/C	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151708795	aacttcttccatagt[A/C]ttccctgtctcaata	4703
rs6750342	snp	A/G	0.36315	0.222928	intron-variant	NEB	GRCh38.p7	2:151629240	GAGGCTCTATGCTCA[A/G]AATATGGAGATGAAT	4703
rs6750662	snp	G/T	0.0111196	0.0737302	intron-variant	NEB	GRCh38.p7	2:151726826	tggccaggagtttac[G/T]accatcctgggcaac	4703
rs6752115	snp	A/G	0.00478085	0.0486577	intron-variant	NEB	GRCh38.p7	2:151722009	TATGAAGAGGGTGGC[A/G]TTAAAAATTAGACCT	4703
rs6755280	snp	A/G	0.0242094	0.107325	intron-variant	NEB	GRCh38.p7	2:151698101	aaaacaaaacaaaaa[A/G]aaaaaaaCCTGACAA	4703
rs6756349	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151635191	gctcttagcaaagag[G/T]tctcaatacttcttg	4703
rs6759419	snp	A/G	0.369958	0.21934	intron-variant	NEB	GRCh38.p7	2:151693189	ATATTACTTGTCTGT[A/G]TTTCTTTTCTGCTAG	4703
rs6760384	snp	C/T	0.48995	0.0701706	intron-variant	NEB	GRCh38.p7	2:151731300	CTTTTTTTAGAGCTG[C/T]GCCACTAATTAGATA	4703
rs6760683	snp	C/T	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151716428	aggtgtgagccaccg[C/T]gcctggccAATATCA	4703
rs7419413	snp	C/T	0.453575	0.145111	intron-variant	NEB	GRCh38.p7	2:151561508	GACTGAGACTGGGGT[C/T]GAGATTTTGGCCATT	4703
rs7419956	snp	C/T	0.466721	0.124627	intron-variant	NEB, RIF1	GRCh38.p7	2:151502418	TAAAAGCTGCAAACA[C/T]AAAGAATACATTAAA	4703
rs7420102	snp	C/T	0	0	intron-variant	NEB	GRCh38.p7	2:151688186	TTACAAAGTAACCAT[C/T]TTAAAGTTGTTTATT	4703
rs7421893	snp	A/G	0.456803	0.140473	intron-variant	NEB	GRCh38.p7	2:151572620	gcacgatctcagctc[A/G]ctgcaacctctgcct	4703
rs7422136	snp	C/T	0.455502	0.142369	intron-variant	NEB	GRCh38.p7	2:151577803	AGGCTGATCTTGAAA[C/T]TCTGGACCTTGTGAT	4703
rs7423252	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151591071	AGAATTCTCTGTACT[A/G]TGAAATTAAATCTCT	4703
rs7424331	snp	C/T	0.453453	0.145282	intron-variant	NEB	GRCh38.p7	2:151561485	TGCCAGAATGAATAG[C/T]TTCTCTTGACTGAGA	4703
rs7426114	snp	C/T	0.386175	0.209658	missense	NEB	GRCh38.p7	2:151671058	TATGCTGAGCCAACA[C/T]CATGCCCATGGAATC	4703
rs7557092	snp	A/T	0.294064	0.246086	intron-variant	NEB	GRCh38.p7	2:151566945	GCAGCAGATTTTTTT[A/T]AAAAAAATTTGATTG	4703
rs7557801	snp	A/G	0.375996	0.215928	intron-variant	NEB	GRCh38.p7	2:151730144	ATAATAAGATCCCAA[A/G]GTATATCCACATCTC	4703
rs7558940	snp	C/G	0.467132	0.12391	intron-variant	NEB, RIF1	GRCh38.p7	2:151511541	CCAGAGTTGGACCAG[C/G]GAATCTACATCCCCA	4703
rs7559359	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151717679	TTGCTGAATTTTCTT[C/G]CCTCCTCCTCAAGAC	4703
rs7561515	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151660163	TTCAGTTCAGTGCAG[A/G]TCTCTACTGACAGAG	4703
rs7563441	snp	A/G	0.48378	0.0885831	intron-variant	NEB	GRCh38.p7	2:151710099	AAATTAATCAATTTC[A/G]TAACTGTACAATTTG	4703
rs7563568	snp	A/G	0.467234	0.12373	intron-variant	NEB	GRCh38.p7	2:151544191	CCTCAGTGCTGATGC[A/G]CAACTTGCCCAAAAT	4703
rs7564024	snp	C/T	0.466824	0.124448	intron-variant	NEB	GRCh38.p7	2:151678621	GTAGGATGTTAATAT[C/T]AATGATAGTAGAATT	4703
rs7564674	snp	C/T	0.495056	0.049474	intron-variant	NEB	GRCh38.p7	2:151684620	CAGTTCTTCCTAACC[C/T]TGAAGGGCATGCTCT	4703
rs7566225	snp	C/T	0.467234	0.12373	intron-variant	NEB, RIF1	GRCh38.p7	2:151513277	CATCAAATGAGTGGA[C/T]TGACTCAGAAATAAG	4703
rs7567137	snp	C/T	0.00478085	0.0486577	intron-variant	NEB	GRCh38.p7	2:151654936	aagggatcctcctgc[C/T]tcagcttcctgagta	4703
rs7568873	snp	A/G	0.456332	0.141164	intron-variant	NEB	GRCh38.p7	2:151570735	TAAAGAAGAGCATAG[A/G]TGAGAATCATTCTAT	4703
rs7572497	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151717158	GTCAAGTGACATTAG[A/G]ACATGGCTTCTGTTT	4703
rs7572749	snp	A/G	0	0	intron-variant	NEB	GRCh38.p7	2:151717393	TCTTCAAGGGAGGCA[A/G]TGTCCCAGCTCTATT	4703
rs7575451	snp	C/G	0.455039	0.143036	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151496329	TCTCGGGAGTGACAG[C/G]TAAAGGAGTTCCCTT	4703
rs7577146	snp	G/T	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151715235	gaaggaaacatgtgg[G/T]aaataactttaataa	4703
rs7583401	snp	C/T	0.00517822	0.0506191	intron-variant	NEB	GRCh38.p7	2:151654654	TTTCCATGGGCCAGG[C/T]ACTGTATTGAGAATC	4703
rs7584016	snp	C/T	0.0205511	0.0992634	intron-variant	NEB	GRCh38.p7	2:151664226	CCTCCTGGTAAAACA[C/T]GTAGATTGCATCTTT	4703
rs7585717	snp	A/G	0.45692	0.1403	intron-variant	NEB, RIF1	GRCh38.p7	2:151525685	GGCCACTCCTAATCA[A/G]CAATGTTTCCTTCTG	4703
rs7587301	snp	A/G	0.445196	0.1562	intron-variant	NEB, RIF1	GRCh38.p7	2:151491086	CTCAGGCTGAAGGGC[A/G]GTGGTACAATCACGG	4703
rs7591363	snp	C/T	0.206029	0.246103	intron-variant	NEB	GRCh38.p7	2:151722048	GGAGACACCATCAAA[C/T]TGGTGTGTATAATTT	4703
rs7592236	snp	C/T	0	0	intron-variant	NEB	GRCh38.p7	2:151591719	CAGAAAAAAACATAT[C/T]GCTTGGCTTTTACAA	4703
rs7596907	snp	A/G	0.000684039	0.0184811	intron-variant	NEB	GRCh38.p7	2:151653955	TCACCTGATTCAGAT[A/G]AAAATATAGCCTTAT	4703
rs7597735	snp	A/G	0.482083	0.0929373	intron-variant	NEB, RIF1	GRCh38.p7	2:151525815	TGGGTCATTTTAAAA[A/G]TCAGAGTTTAAGATT	4703
rs7602626	snp	A/G	0.00279162	0.0372561	intron-variant	NEB	GRCh38.p7	2:151660416	GATTTCTATAGGGTA[A/G]TGATACCTGAGTTTT	4703
rs7602715	snp	A/G	0.401215	0.199083	intron-variant	NEB	GRCh38.p7	2:151565423	TACAAGCAATTATCT[A/G]AAGTTAAGCTAATCC	4703
rs7602828	snp	C/T	0.467234	0.12373	intron-variant	NEB	GRCh38.p7	2:151544218	AAATCCCTCTGGGAA[C/T]TGGGAAGAGGAGAAA	4703
rs9287979	snp	A/G	0.497182	0.037434	intron-variant	NEB, RIF1	GRCh38.p7	2:151499847	TTGTAGAGATGGTCA[A/G]GTATAGAGGTTCAAT	4703
rs9287981	snp	A/G	0.462472	0.13174	intron-variant	NEB	GRCh38.p7	2:151539826	ATGCAATTAAGAGAA[A/G]AAAGGGAACAAACAT	4703
rs9287982	snp	A/G	0.462582	0.131564	intron-variant	NEB	GRCh38.p7	2:151539927	ATCACAATTCTCATT[A/G]TCATTCCACATATAT	4703
rs9287983	snp	A/C	0.499035	0.0219437	intron-variant	NEB	GRCh38.p7	2:151544797	CAGCCATCAGAGCTA[A/C]TGAGAAGGATGAAAT	4703
rs9287990	snp	A/G	0.468349	0.121752	intron-variant	NEB	GRCh38.p7	2:151660317	AATTTTCATCTTAGC[A/G]TCTCCTTTCAGAAAC	4703
rs9677191	snp	C/T	0	0	intron-variant	NEB	GRCh38.p7	2:151703228	ttctgctgagagatc[C/T]gctgttagtctgatg	4703
rs9750717	snp	A/G	0.418007	0.185132	intron-variant	NEB	GRCh38.p7	2:151557690	caagtcagcttcatc[A/G]ctgggatgcaagcct	4703
rs9751624	snp	A/G	0.4087	0.193169	intron-variant	NEB	GRCh38.p7	2:151557411	agtccaggaccagat[A/G]gattcacacctggat	4703
rs10165921	snp	A/G	0.444	0.157683	intron-variant	NEB	GRCh38.p7	2:151730830	GTTAACAATCGTCTA[A/G]AACTTGCCTAATGTT	4703
rs10167358	snp	G/T	0.330947	0.236533	intron-variant	NEB	GRCh38.p7	2:151578178	AGGAAATAAATAACC[G/T]TCTGTAATCCATCAT	4703
rs10170273	snp	C/T	0.421464	0.181934	NEB	2	allele_origin=T(germline)/C(germline)	2:151664582	TCCTTTCTTCTTTTC[C/T]TCTTCCCAGCCAGCT	4703
rs10172023	snp	C/G	0.411049	0.191215	missense, intron-variant	NEB	GRCh38.p7	2:151619514	GTCGGGCAGGCAGAT[C/G]CATTCATGCAGAGGA	4703
rs10172692	snp	A/G	0.461592	0.133149	intron-variant	NEB	GRCh38.p7	2:151732794	CAGAACTTTCTCTTC[A/G]TCTCTGTCCCTTTGA	4703
rs10173335	snp	A/T	0.122667	0.21515	intron-variant	NEB	GRCh38.p7	2:151656478	TACTGTGAAGAAAAT[A/T]TGAGTTTTTACACAG	4703
rs10174077	snp	C/T	0.39009	0.207062	intron-variant	NEB	GRCh38.p7	2:151625198	AGAAAATAAACTTGC[C/T]GCACAAATTTTGAAG	4703
rs10174130	snp	C/T	0.46845	0.121572	intron-variant	NEB	GRCh38.p7	2:151550103	AAGATCCCACCTCTA[C/T]AAAAAATTTTAAAAT	4703
rs10178880	snp	C/T	0.494013	0.0543839	intron-variant	NEB	GRCh38.p7	2:151657251	AGGGAAGATGAAGAA[C/T]AGAGATGGGAGAGAA	4703
rs10182296	snp	A/G	0.476746	0.10529	intron-variant	NEB, RIF1	GRCh38.p7	2:151515219	ATGGATGCACCATCA[A/G]GACTCTGAATCCTCT	4703
rs10185966	snp	A/G	0.376989	0.215346	intron-variant	NEB	GRCh38.p7	2:151726009	CTGAATTAATGGCAG[A/G]TCTGAATTATATTCT	4703
rs10186482	snp	A/G	0.49621	0.0433651	intron-variant	NEB	GRCh38.p7	2:151625463	ATGAGGATTAATTTC[A/G]TAATTCTCACATTCC	4703
rs10186656	snp	G/T	0.44933	0.15097	intron-variant	NEB	GRCh38.p7	2:151619424	GATCCGCTTTTAACA[G/T]GCAGAGCTAACATCA	4703
rs10186956	snp	C/T	0.0271762	0.113356	intron-variant	NEB	GRCh38.p7	2:151544368	AGGAGAGATGTGGTG[C/T]Ggtggttttcaacac	4703
rs10187997	snp	C/T	0.462582	0.131564	intron-variant	NEB	GRCh38.p7	2:151539455	CCTTCTCTTTTCTGC[C/T]TCGGGCTTACTGCAA	4703
rs10192459	snp	C/T	0.180383	0.240111	intron-variant	NEB	GRCh38.p7	2:151661465	TAGATCCAAATCATC[C/T]TTTTCTCTGTTATCA	4703
rs10193188	snp	A/G	0.488118	0.0761554	intron-variant	NEB	GRCh38.p7	2:151694696	GACCTTTAAAGACTA[A/G]TGGGTAACTAAATAC	4703
rs10199238	snp	A/G	4.3555e-05	0.00466643	intron-variant	NEB, RIF1	GRCh38.p7	2:151490357	ACTGCCAAAATCAGC[A/G]CCAGGCACTTGTACC	4703
rs10202662	snp	A/G	0.206947	0.246265	intron-variant	NEB	GRCh38.p7	2:151727299	CATACCTTTTTATAT[A/G]CTGTTAGCTAGTCTA	4703
rs10203078	snp	A/G	0.0271762	0.113356	intron-variant	NEB	GRCh38.p7	2:151540131	ATATTTTTATTCAGG[A/G]GAGAATTGAGAAGAA	4703
rs10208825	snp	A/G	0.46865	0.121211	intron-variant	NEB	GRCh38.p7	2:151547168	AGTTGGAATGATTCC[A/G]TGTTGAATGTAGAAT	4703
rs10210564	snp	A/G	0.449091	0.151204	intron-variant	NEB, RIF1	GRCh38.p7	2:151532192	ACCTCCACCTCCCAG[A/G]TTCAAGCAATTCTTC	4703
rs10432479	snp	C/T	0.475789	0.107327	intron-variant	NEB, RIF1	GRCh38.p7	2:151509261	AGAAACGGTAGTTCA[C/T]CATGAACAAATGTTT	4703
rs10432480	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151703020	tgctttccatgttta[C/G]cgcttccttcagaag	4703
rs10497081	snp	G/T	0.323434	0.238972	intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151496881	TAATATGTATTATTT[G/T]AAATCATGAAATAGT	4703
rs10497082	snp	C/T	0.32153	0.239548	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151498744	TAGGGATATTTGGGT[C/T]TTACAAACATTGTGT	4703
rs10497083	snp	C/T	0.02016	0.0983543	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151499043	CAGTATAAATGTGGA[C/T]GCTTAGACACTGAGA	4703
rs10497084	snp	A/G	0.344147	0.231595	intron-variant	NEB	GRCh38.p7	2:151560022	GATTTAAAGGCATAA[A/G]GAGTTAGAGGATGTA	4703
rs10497085	snp	A/G	0.144632	0.226711	intron-variant	NEB	GRCh38.p7	2:151571758	AACAAATAACAGAGA[A/G]ACTCGGAAATAATAG	4703
rs10529317	in-del	-/ATTT			intron-variant	NEB	GRCh38.p7	2:151574749	TTTATTTATTTATTT[-/ATTT]GAGACAGGGTCTTGC	4703
rs10545796	in-del	-/AGG	0.497803	0.033074	intron-variant	NEB	GRCh38.p7	2:151707515	ATTCAATTTACAAGT[-/AGG]AGGAGGAGGATGGAG	4703
rs10687343	in-del	-/AA/C	0.000238199	0.0109107	intron-variant	NEB	GRCh38.p7	2:151546018	AAAAAAAAAAAAAAA[-/AA/C]CAGAAATACAAGTTG	4703
rs10712295	in-del	-/A	0.497211	0.037236	intron-variant	NEB	GRCh38.p7	2:151729069	AGGTATTTCACCTTG[-/A]AAAAAAAAAGAGCTT	4703
rs10716811	in-del	-/T			intron-variant	NEB	GRCh38.p7	2:151673733	AAATTTTTCTTTTTC[-/T]TTTTTTTTTTTTTTT	4703
rs10803901	snp	A/G	0.4711	0.116682	intron-variant	NEB	GRCh38.p7	2:151730616	GGCTCATTTCTTAGT[A/G]AAAAAAAAAAAAAAA	4703
rs10909569	snp	C/T	0.291976	0.246451	missense, intron-variant	NEB	GRCh38.p7	2:151592126	CTTTCTCCCAGGCAT[C/T]GCGATACAATGGCTG	4703
rs10930688	snp	C/T	0.477515	0.103619	intron-variant	NEB, RIF1	GRCh38.p7	2:151527863	TCTGCCAGTCCAGCC[C/T]AATCATCTTCAGAAT	4703
rs10930723	snp	A/C	0.449528	0.150627	NEB	2	allele_origin=A(germline)/C(germline)	2:151655264	TTAATTTTTATATAA[A/C]TTTACCTGACTATAC	4703
rs10930740	snp	C/T	0.4944	0.0526182	intron-variant	NEB	GRCh38.p7	2:151698050	CAGCCCGGGCGACAA[C/T]GCGAGACTCCGTCTC	4703
rs11305294	in-del	-/T	0.5	0	intron-variant	NEB	GRCh38.p7	2:151689222	TTTTTTTTTTTTTTT[-/T]GAGACCGTGTCTGGC	4703
rs11308757	in-del	-/T			intron-variant	NEB	GRCh38.p7	2:151723751	TACCTGCCTTCTTTG[-/T]TTTTTTTTTTTTTTT	4703
rs11428843	in-del	-/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151500604	TTTTTTTTTTTTTTT[-/T]GAAACAGGGTCTCAC	4703
rs11436329	in-del	-/G	0.0085769	0.0649221	intron-variant	NEB	GRCh38.p7	2:151546309	CAGCTGTGCGGGGGG[-/G]TAATTATGCATTGTG	4703
rs11436330	in-del	-/T			intron-variant	NEB	GRCh38.p7	2:151546575	TTTTTTTTTTTTTTT[-/T]GAGACAGAGTTTCAT	4703
rs11444927	in-del	-/A/AA	0.499866	0.0081858	intron-variant	NEB	GRCh38.p7	2:151671986	AAGGAAAAAAAAAAA[-/A/AA]CACCTTTCCCAAATT	4703
rs11550110	snp	A/G	0.00358779	0.0422022	utr-variant-5-prime	NEB	GRCh38.p7	2:151733727	TTCGGGAAGAAAATA[A/G]CCCCATTGCCTTGAG	4703
rs11676552	snp	C/T	0	0	intron-variant	NEB	GRCh38.p7	2:151689159	AAAACAACAATAATT[C/T]TAAATAAAATACTAG	4703
rs11681815	snp	C/T	0.00438332	0.0466095	intron-variant	NEB	GRCh38.p7	2:151622304	TGTTTGGTAAAGTTT[C/T]GTTTTAATACTTTCA	4703
rs11681877	snp	A/C	0.309154	0.242901	intron-variant	NEB	GRCh38.p7	2:151622456	ATGTATACTTTCCAC[A/C]TTTTGCAAAACTTCA	4703
rs11682211	snp	G/T	0.00947846	0.0681864	intron-variant	NEB	GRCh38.p7	2:151658624	AAATATCAATACATT[G/T]GCACATTCTTTGTTT	4703
rs11692477	snp	C/T	0.00557542	0.0525036	intron-variant	NEB	GRCh38.p7	2:151730165	TCCACATCTCAATTA[C/T]TCCTATACCCTCCTG	4703
rs11692567	snp	A/G	0.17138	0.237316	intron-variant	NEB	GRCh38.p7	2:151706441	GGGCTCTTAATAATT[A/G]CACAATTAGAAAGTC	4703
rs11693227	snp	A/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151630469	GACAATCCTCTGAAG[A/T]GTCTAAAATACTACT	4703
rs11695285	snp	C/T	0.116838	0.211584	intron-variant	NEB, RIF1	GRCh38.p7	2:151486160	CGAACTCCTACAACT[C/T]AATGCCTTCCCCCAC	4703
rs11695661	snp	C/T	0.491368	0.0651254	intron-variant	NEB	GRCh38.p7	2:151707836	TCCAAAGGCAAGAGA[C/T]ACACAAGGGAAGCAC	4703
rs11884193	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151700802	atatacaatcatgtc[A/G]tctgcaaacagggac	4703
rs11884800	snp	A/G	0.0325976	0.123435	intron-variant	NEB	GRCh38.p7	2:151554181	GATTAACACCAAGGG[A/G]AATTTTTAAAAAATA	4703
rs11885813	snp	A/T	0.185788	0.241613	intron-variant	NEB	GRCh38.p7	2:151655001	TGTTTGATGCAATTT[A/T]TTTTCAACAATTTTC	4703
rs11892352	snp	A/G	0.0329836	0.124112	intron-variant	NEB	GRCh38.p7	2:151559105	acaagaaaaaaacaa[A/G]caaccccatcaaaaa	4703
rs11892439	snp	A/T	0.361894	0.223562	intron-variant	NEB	GRCh38.p7	2:151613344	GATACTTCCTATAAG[A/T]TAAATAGACACAAAA	4703
rs11894996	snp	A/G	0.0498993	0.149866	NEB	2	allele_origin=G(germline)/A(germline)	2:151552782	TATACTTGATCTGCC[A/G]AGAGGAAGAAAACAA	4703
rs11896217	snp	A/G	0.378568	0.214407	upstream-variant-2KB	NEB	GRCh38.p7	2:151734675	CCTAACTTCCAGCCT[A/G]TGCAGTTCAATTTTA	4703
rs11900107	snp	C/T	0.00947846	0.0681864	intron-variant	NEB	GRCh38.p7	2:151573427	TTGAGTGGGAAGAGG[C/T]GTCTATACTGCAGTG	4703
rs11900790	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151700924	ggagtggtgagagag[A/G]gcatccctgtcttgt	4703
rs11900834	snp	C/T	0.0221141	0.102801	intron-variant	NEB	GRCh38.p7	2:151649611	CATATAATTACTCCA[C/T]CCTGCTATATTTTAT	4703
rs11900890	snp	C/T	0.0829062	0.185956	intron-variant	NEB	GRCh38.p7	2:151569835	TCTATAGAAAGAATA[C/T]TTTCACAGTTTTCTT	4703
rs11902272	snp	A/G	0.0221141	0.102801	intron-variant	NEB	GRCh38.p7	2:151668267	TACTTTTGGAAAAAC[A/G]TTTCTTGTAATGAAG	4703
rs11902616	snp	C/T	0.134325	0.221629	intron-variant	NEB	GRCh38.p7	2:151610487	TCAGCACAGTGGAGA[C/T]CACAGAGAGTTAGAT	4703
rs11902876	snp	G/T	0.444444	0.157135	intron-variant	NEB	GRCh38.p7	2:151723750	CTACCTGCCTTCTTT[G/T]TTTTTTTTTTTTTTT	4703
rs11904536	snp	C/T	0.461703	0.132974	intron-variant	NEB	GRCh38.p7	2:151647876	atattagtgataaaa[C/T]tgaataaattctgta	4703
rs12052407	snp	C/T	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151513486	ATTGTATGCATGTGA[C/T]TGTCACCAATAAATC	4703
rs12052828	snp	A/C	0.493477	0.0567349	intron-variant	NEB	GRCh38.p7	2:151693913	CTTACTTTGCCCTTA[A/C]ATTAATTTCTTTACT	4703
rs12052998	snp	A/T	0.347032	0.230401	intron-variant	NEB	GRCh38.p7	2:151566946	CAGCAGATTTTTTTT[A/T]AAAAAATTTGATTGA	4703
rs12053135	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151524852	tttgtgtttttagta[A/G]agacagggtttcacc	4703
rs12104727	snp	C/T	0.0248432	0.108648	intron-variant	NEB	GRCh38.p7	2:151680320	CACCAACCACCTATA[C/T]TATATTTTGTGGGCA	4703
rs12328396	snp	A/G	0.191461	0.24305	intron-variant	NEB	GRCh38.p7	2:151718562	AAACGCTACACACTT[A/G]TCTTCTCCATATTCA	4703
rs12328501	snp	A/G	0.471004	0.116864	intron-variant	NEB	GRCh38.p7	2:151665025	AACTAAATACACAAT[A/G]AGAAAAAAATTGTTG	4703
rs12328572	snp	C/T	0.0263992	0.111815	intron-variant	NEB	GRCh38.p7	2:151568866	TGGCTTTCTTTTTAG[C/T]ATTTTATTTTTTAAA	4703
rs12464543	snp	A/G	0.48378	0.0885831	intron-variant	NEB	GRCh38.p7	2:151709919	TGTGGTACCATTACA[A/G]AAATGATTAGCAACT	4703
rs12472633	snp	A/G	0	0	intron-variant	NEB	GRCh38.p7	2:151713652	TACAGAGAAACTAAA[A/G]GGACTTTCCAGTGTC	4703
rs12612655	snp	C/G	0.0448719	0.142907	intron-variant	NEB	GRCh38.p7	2:151731636	GGAACAAAATGGTAG[C/G]GATGGGATGTCTAAA	4703
rs12616767	snp	C/T	0.469346	0.119947	intron-variant	NEB	GRCh38.p7	2:151663267	TTTGCTAGACATATT[C/T]CTTTCAATACACTCT	4703
rs12618063	snp	A/C	0.37973	0.213706	intron-variant	NEB	GRCh38.p7	2:151675267	TCCGAATTTCACATC[A/C]CAGCAAAGACCCTAC	4703
rs12618365	snp	A/G	0.0356815	0.128715	intron-variant	NEB	GRCh38.p7	2:151718130	agtgctgggattaca[A/G]gcgtgagccaccgcg	4703
rs12619249	snp	A/G	0.0448719	0.142907	intron-variant	NEB	GRCh38.p7	2:151695051	TAGTACTCATTTATA[A/G]AATTATTGAAGAAAT	4703
rs12620077	snp	A/G	0.373666	0.217271	intron-variant	NEB	GRCh38.p7	2:151663513	GGTTGCTTATTATCC[A/G]GAGTAAACGCTCTGC	4703
rs12622127	snp	C/G	0.0263992	0.111815	intron-variant	NEB	GRCh38.p7	2:151609700	CCCCAGCCCCACCCC[C/G]AGGTTTGTGCAGTGC	4703
rs12623343	snp	G/T	0	0	intron-variant	NEB	GRCh38.p7	2:151623289	CTGGAAAAGAATTTA[G/T]AAATAATGCATGGCT	4703
rs12623597	snp	C/T	0	0	intron-variant	NEB	GRCh38.p7	2:151711377	TGTTAACAGACATAA[C/T]TAATGGGTCTCAAGG	4703
rs12623646	snp	C/G	0.0543475	0.155628	intron-variant	NEB	GRCh38.p7	2:151674950	ctttagaaattttag[C/G]gttgttattttaaaa	4703
rs12624108	snp	G/T	0.039522	0.134904	intron-variant	NEB	GRCh38.p7	2:151647855	tattttcttttctta[G/T]aaaggatattagtga	4703
rs12693088	snp	A/G	0.158962	0.232835	intron-variant	NEB	GRCh38.p7	2:151677122	CTTAGGAGCAAAAAC[A/G]TATATTCATATGTAT	4703
rs12693090	snp	A/C	0.467642	0.123012	intron-variant	NEB	GRCh38.p7	2:151693655	CCACATTTTCTTTAT[A/C]CAATCTATCGTTGTT	4703
rs12996964	snp	C/T	0.319376	0.240181	intron-variant	NEB	GRCh38.p7	2:151536908	AAGAATCATGAGGGG[C/T]TGAACAGAGTTGATT	4703
rs12997759	snp	G/T	0.00398564	0.0444627	intron-variant	NEB	GRCh38.p7	2:151621598	CAAAACTGCAAAACT[G/T]TTTTGACTTCTTCTG	4703
rs12997859	snp	A/G	0.00716266	0.059414	intron-variant	NEB	GRCh38.p7	2:151692808	aaccccgtctctact[A/G]aaaatacaaaaatta	4703
rs12998096	snp	C/G	0.00676609	0.0577691	intron-variant	NEB	GRCh38.p7	2:151671647	GGTGCTGCTAAAAAG[C/G]ATTTTGTCACTTTTG	4703
rs12998234	snp	C/T	0.00394655	0.0442459	missense, intron-variant	NEB	GRCh38.p7	2:151606686	AGCCTTTCTGCTTGG[C/T]GTCATTCCAGTCTTT	4703
rs12998871	snp	C/T			synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151631167	GTTGAGAGCATTGTT[C/T]TTGGCCAGCACCTGC	4703
rs12999032	snp	C/T	0	0	missense, intron-variant	NEB	GRCh38.p7	2:151631184	TGGCCAGCACCTGCT[C/T]TAGAGAATCAGTCAC	4703
rs13012674	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151714198	tccggacctaccaaa[A/G]aagaaaacaattccc	4703
rs13013209	snp	C/G	0.48554	0.0837915	NEB	2	allele_origin=G(germline)/C(germline)	2:151643935	TAAGGTCTGGCACTT[C/G]TTGGCCAACACCACC	4703
rs13013919	snp	A/G	0	0	intron-variant	NEB	GRCh38.p7	2:151661858	TTCAACCTCACCTTA[A/G]ACAAACAGGACTCAT	4703
rs13018522	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151609319	CCAAAAAAGCAAGAC[C/T]TGAGATCTCACATGA	4703
rs13021010	snp	C/T	0.00438332	0.0466095	intron-variant	NEB	GRCh38.p7	2:151552266	ATTAAGTGCTTTTCA[C/T]AAGCCTTATAGATAA	4703
rs13023600	snp	C/T	0.00676609	0.0577691	intron-variant	NEB, RIF1	GRCh38.p7	2:151512603	ACAGACGTGAGCCAC[C/T]GCACCTGGTGAATCT	4703
rs13024542	snp	A/C	0	0	missense, intron-variant	NEB	GRCh38.p7	2:151631177	TTGTTCTTGGCCAGC[A/C]CCTGCTCTAGAGAAT	4703
rs13025954	snp	C/T	0.204496	0.245824	intron-variant	NEB	GRCh38.p7	2:151728506	TTAATTAATGTGAAC[C/T]GGAGTGCCATTTACA	4703
rs13028859	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151576546	ttttttttttttttt[C/T]tttgagacagagtct	4703
rs13031275	snp	A/C	0.0841707	0.187085	NEB, RIF1	2	allele_origin=A(germline)/C(germline)	2:151489980	ACTTACTCCAGCAGT[A/C]GATGGATGAGATGGG	4703
rs13032138	snp	A/G	0.488666	0.0744214	intron-variant	NEB	GRCh38.p7	2:151639524	TTTATGCACATCTTC[A/G]GGTAATAAGTTCATA	4703
rs13032358	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151531305	AACTCTCTTTTTTTC[C/T]ttctttttttttttt	4703
rs13032364	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151531309	CTCTTTTTTTCtttc[C/T]ttttttttttttttt	4703
rs13383484	snp	C/T	0.468148	0.122112	intron-variant	NEB	GRCh38.p7	2:151633040	CAAATTAGTTTTAGT[C/T]TCCAAAACTTGCTAG	4703
rs13384856	snp	C/T	0.171057	0.237209	intron-variant	NEB	GRCh38.p7	2:151708963	ACGTGGATGCTGTAA[C/T]AGCCTTCTAAGTGAT	4703
rs13387601	snp	A/G	0.0452528	0.143452	intron-variant	NEB	GRCh38.p7	2:151715250	gaaataactttaata[A/G]tacagtttactgaac	4703
rs13389497	snp	A/G	0	0	intron-variant	NEB, RIF1	GRCh38.p7	2:151531641	ctttattggggagga[A/G]aatcctgtgcataac	4703
rs13391309	snp	C/T	0.46885	0.12085	intron-variant	NEB, RIF1	GRCh38.p7	2:151519421	ATGCACTCTCTAAAA[C/T]AGGCAAATGCATAGA	4703
rs13393021	snp	A/C	0.420096	0.183214	intron-variant	NEB	GRCh38.p7	2:151556744	acagagagacttaga[A/C]tgcaacacaataata	4703
rs13393122	snp	A/G	0.319616	0.240112	intron-variant	NEB	GRCh38.p7	2:151556801	acactagacagatca[A/G]ccagacagaaaatta	4703
rs13394721	snp	C/T	0.0356815	0.128715	intron-variant	NEB	GRCh38.p7	2:151686906	CATGAAAAGAAATGT[C/T]CATTTTCTAGATAGA	4703
rs13399526	snp	A/G	0	0	intron-variant	NEB	GRCh38.p7	2:151685498	AGATAACCCCACTGA[A/G]AATCTCAAAGGTTGT	4703
rs13399785	snp	A/G	0.0513262	0.151752	intron-variant	NEB	GRCh38.p7	2:151655667	AAAAAATAAGAGATG[A/G]GCAGAAGAAGATGGT	4703
rs13404704	snp	A/G	0.471578	0.115772	intron-variant	NEB	GRCh38.p7	2:151651915	CTGACCTGACCTTCC[A/G]TATCAAGAAAACAAC	4703
rs13405323	snp	C/T	0.0142736	0.0832652	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151498958	GGTTAGAATAAGAAA[C/T]GAGGATAATAGTCGG	4703
rs13407334	snp	C/T	0.0744748	0.178019	intron-variant	NEB	GRCh38.p7	2:151665199	ACATAATGGAAGCAA[C/T]AGAGTCCCCCTCCCA	4703
rs13409931	snp	A/G	0	0	intron-variant	NEB, RIF1	GRCh38.p7	2:151512444	gatcttcccacctca[A/G]ccttcctagaagctg	4703
rs13413290	snp	C/T	0.0463947	0.145069	intron-variant	NEB	GRCh38.p7	2:151546149	AGCAAAAACAATTGT[C/T]ATTTAACTAAGCTCA	4703
rs13425109	snp	C/G	0.49681	0.0398085	intron-variant	NEB	GRCh38.p7	2:151537592	GTTGTCACTTCATTG[C/G]ATCAAAATAGGCTAT	4703
rs13425170	snp	A/C	0.301681	0.2446	intron-variant	NEB, RIF1	GRCh38.p7	2:151530598	AATTCATTTTTAAAA[A/C]ATCAGTACCTCAGGA	4703
rs13426673	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151641488	ggcatgcgccatcac[A/C]cctggctaattttta	4703
rs13427102	snp	C/T	0.137433	0.223223	NEB	2	allele_origin=T(germline)/C(germline)	2:151680837	ATTTTTTCTGTTTGG[C/T]AAATCAAAAAGAGAA	4703
rs13428975	snp	C/T	0.490453	0.0684267	intron-variant	NEB	GRCh38.p7	2:151641117	CAATAAAAATTATCT[C/T]TGCCTGCAAAGAATG	4703
rs13429205	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151641359	gtAttttagaaagca[C/T]ctctctctgttgccc	4703
rs13429567	snp	A/G	0.182933	0.240836	intron-variant	NEB	GRCh38.p7	2:151647857	ttttcttttcttata[A/G]aggatattagtgata	4703
rs16830090	snp	A/G	0.410657	0.191544	intron-variant	NEB, RIF1	GRCh38.p7	2:151485967	AAGGGGAAATATTAT[A/G]TGTTGGATTTGCAAC	4703
rs16830094	snp	A/C	0.117537	0.212022	intron-variant	NEB, RIF1	GRCh38.p7	2:151488297	GATCAAATTGGCCAG[A/C]CTTTTATACTTCTAG	4703
rs16830096	snp	A/G	0.35445	0.227135	intron-variant	NEB, RIF1	GRCh38.p7	2:151488692	CTTTGTACTTCTACA[A/G]TTTTGTATTTTACAT	4703
rs16830106	snp	G/T	0.0919752	0.193722	intron-variant	NEB, RIF1	GRCh38.p7	2:151496076	TGTTACTTCTTGATA[G/T]TAGAACTTTATGGAT	4703
rs16830109	snp	C/T	0.093777	0.195178	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151498701	AACCAAGGAAGTTAC[C/T]TTTGATTTGAAAATG	4703
rs16830114	snp	A/C	0.0916144	0.193427	intron-variant	NEB, RIF1	GRCh38.p7	2:151500288	TATATTTAAACTGAC[A/C]ATTAAAAATATTTTG	4703
rs16830117	snp	A/G	0.0916144	0.193427	intron-variant	NEB, RIF1	GRCh38.p7	2:151501772	ATCAAATAGCATTCA[A/G]ACTAATTGAAATTAA	4703
rs16830125	snp	A/G	0.130008	0.219321	intron-variant	NEB, RIF1	GRCh38.p7	2:151504160	CTAAAGGACTGAATG[A/G]GTTCTTTTAAATGGA	4703
rs16830128	snp	A/G	0.0625487	0.165415	intron-variant	NEB, RIF1	GRCh38.p7	2:151513538	TGTCCTTAAAGTTAC[A/G]ACTACTTTCCTGAAA	4703
rs16830130	snp	A/G	0.0926964	0.194308	intron-variant	NEB, RIF1	GRCh38.p7	2:151513885	CCTCTGGAGGAAACT[A/G]TTCTATGCAAGTCAG	4703
rs16830136	snp	A/G	0.483966	0.0880896	intron-variant	NEB, RIF1	GRCh38.p7	2:151518286	TGTGGATGAATGTGC[A/G]CCAGAGGAAAAATCG	4703
rs16830140	snp	C/T	0.162253	0.234095	intron-variant	NEB, RIF1	GRCh38.p7	2:151523343	TTTTCATAATTCTAA[C/T]TTGTTCTGTCACTTG	4703
rs16830143	snp	A/C	0.0310518	0.120672	intron-variant	NEB, RIF1	GRCh38.p7	2:151525562	GGACTCATATAATAC[A/C]AAGGTTACTACAGCA	4703
rs16830159	snp	C/T	0.350982	0.228698	intron-variant	NEB, RIF1	GRCh38.p7	2:151528703	GCTCATCTAAATGCA[C/T]AAAATTATTTCTGTA	4703
rs16830170	snp	A/G	0.0167857	0.0900616	NEB, RIF1	2	allele_origin=G(germline)/A(germline)	2:151531795	TCTTGCACTTACATC[A/G]CTGATTTGTTTGTTG	4703
rs16830171	snp	C/G/T	0.00179044	0.0298666	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151531823	TTGACTTTTGTAGTA[C/G/T]GCAGGTGTTCTGGAG	4703
rs16830173	snp	C/T	0.0185938	0.0946107	intron-variant	NEB, RIF1	GRCh38.p7	2:151533736	ATGCTTGCGGTTGGC[C/T]ATTCATAGTCCTTGT	4703
rs16830174	snp	C/T	0.0376037	0.131863	intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151534520	GGAGTGTGGGATAGG[C/T]CAGATTTATGACACC	4703
rs16830177	snp	C/T	0.173643	0.238054	intron-variant	NEB	GRCh38.p7	2:151536273	GTAGAACTGCCTAGA[C/T]GTCTTGAAAACTAGC	4703
rs16830186	snp	C/T	0.17332	0.23795	intron-variant	NEB	GRCh38.p7	2:151540093	CCCCAGAAAATGCTG[C/T]TGAAGAATTATAAGA	4703
rs16830189	snp	A/G	0.0154538	0.0865337	intron-variant	NEB	GRCh38.p7	2:151540950	TTTTTTGTTATATGC[A/G]TTTCTGTTCATTTGT	4703
rs16830192	snp	C/G	0.0623228	0.165158	NEB	2	allele_origin=G(germline)/C(germline)	2:151541531	TGACTTCTGCTTCTT[C/G]CCTGCAGCTCTGTAG	4703
rs16830216	snp	A/G	0.00755117	0.0609801	NEB	2	allele_origin=G(germline)/A(germline)	2:151560595	TGCTTTACTTACATG[A/G]CTGGCCAGATGCTTC	4703
rs16830228	snp	A/G	0.347032	0.230401	intron-variant	NEB	GRCh38.p7	2:151563341	TCCTTTTATAACACA[A/G]GGTAAATAGTGACCT	4703
rs16830236	snp	C/T	0.00699791	0.0587366	NEB	2	allele_origin=T(germline)/C(germline)	2:151567211	GCCTGAATAACATCG[C/T]TCTGGTCAGGATGAC	4703
rs17198052	snp	A/G	0.0279526	0.114869	intron-variant	NEB	GRCh38.p7	2:151537491	ACTTTCCTAGATAGT[A/G]TATCATTAGCTTGGC	4703
rs17270233	snp	A/G	0.322959	0.239117	intron-variant	NEB, RIF1	GRCh38.p7	2:151515906	ATTCCAAATAAGCCC[A/G]TTTCCCACTGAAGAC	4703
rs17270269	snp	A/G	0.00874735	0.0655527	intron-variant	NEB	GRCh38.p7	2:151548111	AATCTATGGAACCGA[A/G]TCTCTCCAAGGCATT	4703
rs28375835	snp	A/G	0.336017	0.234736	intron-variant	NEB	GRCh38.p7	2:151643505	AATTCTAAATTTTTG[A/G]TATGAATTATAAATC	4703
rs28439679	snp	A/T	0.0850919	0.187897	intron-variant	NEB	GRCh38.p7	2:151669236	CATTTGTGTTTTCCA[A/T]TTACGAGACAAATAC	4703
rs28705680	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151600018	AAGATGGCGAAAACC[C/T]GCCTCTAATAAAAAT	4703
rs28762756	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151702346	ATGTATATTCTGTTG[A/G]TTTGGGGTGGAGAGC	4703
rs28771721	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151703592	CTAAACTTCCCTTCT[C/T]GCTTCATTTCATTCA	4703
rs28827472	snp	C/G	0	0	intron-variant	NEB	GRCh38.p7	2:151703501	TTCAGGTACACCAAT[C/G]AGACGTAGATTTGGT	4703
rs33988153	snp	C/T	0.318113	0.240542	NEB	2	allele_origin=T(germline)/C(germline)	2:151575797	AACCTCTCTGTACTT[C/T]GGCTGTGGAAAGAAA	4703
rs34024883	in-del	-/T			upstream-variant-2KB	NEB	GRCh38.p7	2:151735925	ATGCTTTAAAATGTG[-/T]TGTTGAATTAAAAAA	4703
rs34036703	in-del	-/G			intron-variant	NEB	GRCh38.p7	2:151554423	CTTAGCTGGGTGTGG[-/G]TGGTGCATGCCTGTA	4703
rs34057391	in-del	-/C			intron-variant	NEB	GRCh38.p7	2:151729391	AAATAGGGGGAACCA[-/C]CCCCCTGCCATCTTG	4703
rs34065332	in-del	-/T			intron-variant	NEB	GRCh38.p7	2:151712605	CCAAGTCTGGGAAGA[-/T]TTTTCATGACACAGG	4703
rs34076280	in-del	-/C			intron-variant	NEB	GRCh38.p7	2:151665301	AACACCATGAGGGTT[-/C]CCCTGGGCGAGGCTG	4703
rs34086514	in-del	-/C			intron-variant	NEB	GRCh38.p7	2:151690175	AAGCACTGCTGTTTT[-/C]CCCCCGATCTTGGCA	4703
rs34116466	in-del	-/AA/AAA/AAAAAA			intron-variant	NEB	GRCh38.p7	2:151719886	GTGAGACCCTGTCTC[-/AA/AAA/AAAAAA]AAAAAAAAAAAAAAA	4703
rs34170221	in-del	-/C			intron-variant	NEB	GRCh38.p7	2:151657345	TCATTAAATGTTCCC[-/C]TGTGAGTGGATTTCT	4703
rs34182658	in-del	-/AAG			intron-variant	NEB	GRCh38.p7	2:151628904	ACAAAAACAAAAGAA[-/AAG]AAGAAGAAGAAGAAG	4703
rs34192896	in-del	-/C			intron-variant	NEB, RIF1	GRCh38.p7	2:151519871	ATGCATTGTACATAG[-/C]AGTGATCATATAATC	4703
rs34219954	snp	G/T	0.143284	0.226079	intron-variant	NEB, RIF1	GRCh38.p7	2:151509342	AAAACAGTTCTCATT[G/T]TCCTGGGAAAAGAAT	4703
rs34234609	snp	A/C	0.00416181	0.0454267	missense	NEB	GRCh38.p7	2:151675340	AAATACACCATGAGT[A/C]CTGATCTTCCTCAGT	4703
rs34238937	in-del	-/C			intron-variant	NEB	GRCh38.p7	2:151690994	TCTCTCTCTCTTTTT[-/C]CCTTTAATCCCCACT	4703
rs34247624	in-del	-/G			intron-variant	NEB	GRCh38.p7	2:151654165	AATAGATTATTAGGG[-/G]AAAAGTTTACCTACA	4703
rs34288939	in-del	-/T			frameshift-variant	NEB	GRCh38.p7	2:151555022	GAGCTTTGAACTTTT[-/T]CATATTCTTCCCGAT	4703
rs34295833	in-del	-/T			intron-variant, utr-variant-3-prime	NEB, RIF1	GRCh38.p7	2:151497300	TTTTTTTTCCTTTTT[-/T]GTGAGTACCATGCCT	4703
rs34351322	in-del	-/T			intron-variant	NEB	GRCh38.p7	2:151649215	AAATGCTTAAACATT[-/T]CATAATGAAGCTGAC	4703
rs34364750	in-del	-/G			intron-variant	NEB	GRCh38.p7	2:151650556	TATATAAACTATTGG[-/G]ATTTAATAGAAACTG	4703
rs34366405	in-del	-/C			intron-variant	NEB	GRCh38.p7	2:151676193	AATAGCTAAATTAAT[-/C]CCCCAAATAATAAAT	4703
rs34368668	snp	C/T	0.00686583	0.0581874	NEB, RIF1	2	allele_origin=T(germline)/C(germline)	2:151506970	GTAAAGGAAAAATTA[C/T]AGTTGTTCAAGACAC	4703
rs34390104	in-del	-/A			intron-variant	NEB	GRCh38.p7	2:151547160	AGTGAGGAGTTGGAA[-/A]TGATTCCATGTTGAA	4703
rs34415027	in-del	-/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151490092	GCTGAAAAAAAGGGG[-/G]CAAATTCTTTATAAG	4703
rs34446552	snp	A/G	0.0209421	0.100162	intron-variant	NEB, RIF1	GRCh38.p7	2:151517833	CTCCATTATAATCTT[A/G]TGGGACCACTGTCAT	4703
rs34471889	snp	A/G	0.00135723	0.0260149	missense	NEB	GRCh38.p7	2:151563646	TCGGTGAATTCCCTG[A/G]TGTGGTTCACTGTCT	4703
rs34482239	in-del	-/A			intron-variant	NEB	GRCh38.p7	2:151553549	AAAAATTGACCATAA[-/A]TAACTTTAACACTAA	4703
rs34484326	in-del	-/AAAT			intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151499037	CAAAGCAGTATAAAT[-/AAAT]GTGGATGCTTAGACA	4703
rs34504204	snp	A/G/T	0.00128874	0.0253528	missense	NEB	GRCh38.p7	2:151565084	CACCAGATACACCAC[A/G/T]TATCTCCCACTCCAA	4703
rs34532796	snp	C/T	0.00377857	0.0433014	missense	NEB	GRCh38.p7	2:151662200	CCAGACACTTTGAAG[C/T]ATTCCACACTCATGG	4703
rs34533053	in-del	-/C			intron-variant	NEB	GRCh38.p7	2:151631628	TAATTATAACATCCC[-/C]TATGCAGGGAAGAAT	4703
rs34555492	snp	C/T	0.0308361	0.12028	NEB	2	allele_origin=T(germline)/C(germline)	2:151540718	GAAGCATGCTAAAGA[C/T]GTGAAGGACATGGTC	4703
rs34556044	snp	A/G	0.0253123	0.109615	missense	NEB	GRCh38.p7	2:151563879	TATGGCTACACCCTG[A/G]ATGAGCGCTACATTC	4703
rs34563404	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151692975	AGCCTGTCTCAAAAA[A/C]CAAAGAAGGAAAGAA	4703
rs34577613	snp	A/G	0.307621	0.243269	NEB	2	allele_origin=G(germline)/A(germline)	2:151671094	CAGCACCCAGATACC[A/G]TCAAGTTCACAAGTG	4703
rs34579746	snp	C/G	0.12932	0.218944	intron-variant	NEB	GRCh38.p7	2:151631935	AAAATATCTGTAATG[C/G]CTTTAAAAACACAGT	4703
rs34591082	in-del	-/G			intron-variant	NEB	GRCh38.p7	2:151561841	TCAACTAAGGTACAG[-/G]ATGCTTGAGAGTAGT	4703
rs34668892	in-del	-/C			intron-variant	NEB	GRCh38.p7	2:151662424	AACATTCTGTAACTT[-/C]CCATTTCATTTGTAA	4703
rs34689224	in-del	-/T			intron-variant	NEB	GRCh38.p7	2:151553037	TACAGTATTTAATTT[-/T]GCGTGGAAAATCCTC	4703
rs34709490	in-del	-/T			intron-variant	NEB	GRCh38.p7	2:151683656	CAGAAAACAGTATGG[-/T]GGTTCCTCTACAAAT	4703
rs34713837	in-del	-/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151523267	TTACATAGGAATTTT[-/T]AAGTTTAAAAACTTT	4703
rs34718443	snp	C/T	0.00494224	0.0494641	NEB, RIF1	2	allele_origin=T(germline)/C(germline)	2:151529225	AGCCAAGGACGCCTA[C/T]AAAGTCAACACCAAT	4703
rs34733773	in-del	-/GGC	0.379561	0.213855	intron-variant	NEB	GRCh38.p7	2:151717388	AGAGTCTTCAAGGGA[-/GGC]GGCAATGTCCCAGCT	4703
rs34754792	in-del	-/C			intron-variant	NEB	GRCh38.p7	2:151695484	TCTTCTCATTTTTAA[-/C]CATTAATCTATTCAT	4703
rs34764042	in-del	-/G			intron-variant	NEB	GRCh38.p7	2:151712554	GAAATGGGTCAGGGT[-/G]GGAGATCGAGCTCTC	4703
rs34766430	in-del	-/G			frameshift-variant, intron-variant	NEB, RIF1	GRCh38.p7	2:151531828	TTTGTAGTACGCAGG[-/G]TGTTCTGGAGTATCC	4703
rs34778227	snp	C/G	0.0266618	0.112339	missense	NEB	GRCh38.p7	2:151663813	AAGGGAAACACATTG[C/G]CTTCCGGAGCCTGGA	4703
rs34784156	in-del	-/A/AA	0.5	0	intron-variant	NEB	GRCh38.p7	2:151656848	AGATGAAAAAAAAAA[-/A/AA]GGCAAAAAAACAGAA	4703
rs34788064	in-del	-/T			intron-variant	NEB	GRCh38.p7	2:151562002	GCTTTGGTCAGTTAG[-/T]AGCCTACACTGTTAC	4703
rs34800215	snp	C/G	0.0393845	0.134689	NEB	2	allele_origin=G(germline)/C(germline)	2:151671122	CGATGCATTAAATGA[C/G]AGGAAGTATCGACAG	4703
rs34816284	in-del	-/A	0.5	0	intron-variant	NEB, RIF1	GRCh38.p7	2:151502388	TAAACATCTAAACAT[-/A]AAAAAAAAAAAACTT	4703
rs34821635	in-del	-/A			intron-variant	NEB, RIF1	GRCh38.p7	2:151517100	AATGCAGCCAATAAA[-/A]TTGGTATAAAAATGA	4703
rs34829854	in-del	-/C			intron-variant	NEB	GRCh38.p7	2:151547167	AGTTGGAATGATTCC[-/C]ATGTTGAATGTAGAA	4703
rs34849956	in-del	-/C			intron-variant	NEB	GRCh38.p7	2:151663155	AGTGGTAGAATGAAA[-/C]CCCGGTTGGGAGGGA	4703
rs34875514	in-del	-/A			intron-variant	NEB	GRCh38.p7	2:151685180	TCTCAAATCAATGAG[-/A]AAACTGTCTGGGTCA	4703
rs34897277	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151691341	CCTTGACCACCCAAC[C/T]TAAGACGCCCATCCA	4703
rs34943165	in-del	-/G			upstream-variant-2KB	NEB	GRCh38.p7	2:151735011	AATAAGATATCCACA[-/G]GGGTGTAATTAGAAA	4703
rs35016946	snp	C/T	0.000516869	0.0160676	synonymous-codon	NEB	GRCh38.p7	2:151665390	GCTGAAGTTCACTTA[C/T]GCCATGGACACAATG	4703
rs35059848	in-del	-/CA	0.45843	0.138046	intron-variant	NEB	GRCh38.p7	2:151656599	TAGAGCTCTATAGTT[-/CA]CAGACTAATTTTTCA	4703
rs35086293	in-del	-/C			intron-variant	NEB	GRCh38.p7	2:151550872	CTGGTCTTGAACTCC[-/C]AGGCTCAAGCCATCT	4703
rs35087623	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151550292	AAAAAAAAAAAAAAC[A/T]CTAATTCCTCTGTGC	4703
rs35092454	in-del	-/A			intron-variant	NEB	GRCh38.p7	2:151554213	GCATTATAGCTGAAA[-/A]TAATATGTAGCTTCT	4703
rs35110901	in-del	-/T	0.210909	0.246925	intron-variant	NEB	GRCh38.p7	2:151726889	TAGGAGATCCTACAA[-/T]TTTTTTTTTAATTAG	4703
rs35134311	in-del	-/T			intron-variant	NEB	GRCh38.p7	2:151683655	CAGAAAACAGTATGG[-/T]TGGTTCCTCTACAAA	4703
rs35134482	snp	C/T	0.029116	0.117091	intron-variant	NEB	GRCh38.p7	2:151672183	CAGCATCAATAATTA[C/T]GATATAAGCACAGAA	4703
rs35153662	in-del	-/T			intron-variant	NEB	GRCh38.p7	2:151726409	AGTGAGCTGCTATCA[-/T]TTTAATGAAAAGTGA	4703
rs35172004	snp	A/T	0.35574	0.226537	intron-variant	NEB	GRCh38.p7	2:151642987	CGGTATTTGTGACAT[A/T]TTCAGGTCTAAATGT	4703
rs35181329	in-del	-/T			intron-variant	NEB	GRCh38.p7	2:151708372	GCAGACTCCACCAAA[-/T]TGCTCTTGTTCAGGT	4703
rs35185037	in-del	-/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151509013	TCCCACTCTTCAGGG[-/G]AAGTTTTAGTTTGTA	4703
rs35194393	snp	A/C	0.000149089	0.00863264	missense	NEB	GRCh38.p7	2:151679765	CTGAGAACTGATGCG[A/C]TTCCCATCAGAGCTG	4703
rs35218518	in-del	-/T			intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151507421	GCCTTCTCTGTTTTT[-/T]CCTGAAGCAGATAAT	4703
rs35227368	snp	A/T	0.0594909	0.161884	NEB	2	allele_origin=T(germline)/A(germline)	2:151576297	TGGATGCCCCAAGGG[A/T]CTCCTGAAGTGTTGA	4703
rs35236177	in-del	-/A	0.5	0	intron-variant	NEB	GRCh38.p7	2:151673436	CACTGTGTAAGTGCT[-/A]AAAAAAAAAAAAAGA	4703
rs35253319	in-del	-/C			intron-variant	NEB, RIF1	GRCh38.p7	2:151508960	CGCTTGTCACTGTCC[-/C]TTTCACTTTTCTCTC	4703
rs35253954	snp	A/T	0.0111196	0.0737302	intron-variant	NEB	GRCh38.p7	2:151569682	ATTTGTACACAAAAA[A/T]TTTTGGATTTTAAAA	4703
rs35273905	snp	A/G	0.00346732	0.0414926	synonymous-codon	NEB	GRCh38.p7	2:151570207	CATGCTTTCCATCCT[A/G]CACTCTAAAAATTCC	4703
rs35292878	snp	A/C	0.0035072	0.0417289	missense, intron-variant	NEB	GRCh38.p7	2:151646152	TTGTTCTGGCTAAAG[A/C]AAACTTAATCAACAC	4703
rs35295005	in-del	-/A			intron-variant	NEB	GRCh38.p7	2:151645253	GTTTTTGTTAGAAAA[-/A]GAGCATCTAATTCTT	4703
rs35307851	in-del	-/T	0.0588605	0.161139	intron-variant	NEB	GRCh38.p7	2:151659675	TGGAAAGTAAAAATG[-/T]TTTTTCCCCTTATCT	4703
rs35318345	in-del	-/A			intron-variant	NEB	GRCh38.p7	2:151671234	TTATACACATTCTGT[-/A]AAAGGGTAAGCTAAT	4703
rs35389145	snp	C/T	0.414741	0.188044	intron-variant	NEB	GRCh38.p7	2:151575374	ATAATTATTTTGAGT[C/T]TATCTGAGTCTATCG	4703
rs35409532	in-del	-/T			intron-variant	NEB	GRCh38.p7	2:151721498	TCACCACCCATGCCC[-/T]TCGGGACCACCACCT	4703
rs35415723	in-del	-/G			intron-variant	NEB	GRCh38.p7	2:151643368	CTGAAAGTGCAAGTG[-/G]ACAAATTTGTCATAA	4703
rs35443024	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151572657	TTCAAACGATTCTTG[G/T]GCCTCAGCCACCCAA	4703
rs35447718	in-del	-/TTA			intron-variant	NEB	GRCh38.p7	2:151550981	TTATTATTATTATTA[-/TTA]TTTGAAACGGAGTTT	4703
rs35488049	in-del	-/A	0.219947	0.248187	intron-variant	NEB	GRCh38.p7	2:151722471	CTGAAGTATCTTCTG[-/A]TAGCAAGAGCTCTTT	4703
rs35499194	snp	G/T	0.5	0	intron-variant	NEB	GRCh38.p7	2:151723777	TTTTTTTTTTTTTGG[G/T]CATTATTTGTCATTG	4703
rs35511860	in-del	-/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151516431	TGTGATGGATCATTG[-/G]TTGTGTGGTGTGGTT	4703
rs35533179	in-del	-/G			intron-variant	NEB	GRCh38.p7	2:151733590	CCCAGCACCAAAATT[-/G]CTAAGAGGGCTGACT	4703
rs35555631	snp	A/G	0.00107595	0.0231694	missense, intron-variant	NEB	GRCh38.p7	2:151643238	GTGACCATGTTTACC[A/G]TCAGCACCCAGATCA	4703
rs35609925	in-del	-/C			intron-variant	NEB, RIF1	GRCh38.p7	2:151533552	ATATTTTCTCTGTCC[-/C]ATGCAAAGAGCAGTG	4703
rs35622063	in-del	-/G			upstream-variant-2KB	NEB	GRCh38.p7	2:151735175	TTTTCTATTAACTCA[-/G]GATGACTCCTGGCTC	4703
rs35625172	snp	A/G	0.0178098	0.0926698	intron-variant	NEB, RIF1	GRCh38.p7	2:151486243	AGCCAAAAAGCACAC[A/G]AAAGGATGCTCAAAA	4703
rs35625617	snp	A/G	0.0514257	0.151882	NEB, RIF1	2	allele_origin=G(germline)/A(germline)	2:151527007	TTTGAATATAAGCTG[A/G]ACCGGGAGTTCCTCA	4703
rs35654397	snp	C/G	0.00424682	0.0458885	synonymous-codon	NEB	GRCh38.p7	2:151672396	GAGTCTTGAGCATAC[C/G]AGGAATGTCAATCAA	4703
rs35676677	in-del	-/T			intron-variant	NEB	GRCh38.p7	2:151687193	ATATTAATGCATACA[-/T]TTTTTCAAAGTGAAA	4703
rs35677134	in-del	-/C	0.0271762	0.113356	intron-variant	NEB	GRCh38.p7	2:151554348	AGAATTGCTTGAGCC[-/C]AGGAGTTTGAGACCA	4703
rs35683184	in-del	-/G			intron-variant	NEB	GRCh38.p7	2:151611646	TTGATAAAATTTTGG[-/G]ATGAAACAAATGATC	4703
rs35686968	snp	C/G	0.0354574	0.128341	NEB	2	allele_origin=G(germline)/C(germline)	2:151724301	CCTCCTGATGCCCCT[C/G]AACTTGTCCAGGCCG	4703
rs35690321	in-del	-/G			intron-variant	NEB	GRCh38.p7	2:151660187	ACAGAGACACTTGAG[-/G]AGCCCTCTGTGGGAC	4703
rs35690604	in-del	-/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151515909	CAAATAAGCCCATTT[-/T]CCCACTGAAGACAGA	4703
rs35696429	in-del	-/AAC			intron-variant	NEB, RIF1	GRCh38.p7	2:151495681	AACAACAACAACAAC[-/AAC]AAACAAAAAACGAAA	4703
rs35707762	snp	C/T	0.0135732	0.081255	NEB	2	allele_origin=T(germline)/C(germline)	2:151548387	AAGCCTATGAACACA[C/T]CAAGGCATATGGGTA	4703
rs35740585	snp	A/G	0.0294045	0.117633	NEB	2	allele_origin=G(germline)/A(germline)	2:151612262	ATCGCCAGCCTGCAG[A/G]CCAGCTCAAATTCAC	4703
rs35751146	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151609578	CTAGCATAATAGCAA[C/G]AATTATTTTAAAAAC	4703
rs35751744	in-del	-/C			intron-variant	NEB	GRCh38.p7	2:151634313	TAAAAGCATGTCAGG[-/C]AAGAGGGTGCACTTG	4703
rs35808744	snp	A/G/T	0.006717	0.0575634	NEB, RIF1	2	allele_origin=G(germline)/A(germline)	2:151506954	AGTTGTTCAAGACAC[A/G/T]CCAGAAATACTGCGT	4703
rs35824119	in-del	-/T	0.474453	0.110094	intron-variant	NEB, RIF1	GRCh38.p7	2:151491038	CTCTACATAATATCC[-/T]TTTTTTTTTTTTTTG	4703
rs35837315	in-del	-/C			intron-variant	NEB	GRCh38.p7	2:151722754	GGTCTTGCTTTACTG[-/C]CCCAGGCTGATCTCC	4703
rs35883641	in-del	-/A	0.169435	0.236663	intron-variant	NEB	GRCh38.p7	2:151733607	TAAGAGGGCTGACTT[-/A]GTTTTCCATACTGCC	4703
rs35886539	snp	A/G	0.5	0	intron-variant	NEB	GRCh38.p7	2:151622104	CTCCCAGGTTCAAGC[A/G]ATTCTCGTGCCTCAG	4703
rs35888911	in-del	-/C			intron-variant	NEB	GRCh38.p7	2:151561696	CACTTTTAACATTCC[-/C]ATTACAACTGCCCTA	4703
rs35891102	in-del	-/A			intron-variant	NEB	GRCh38.p7	2:151689321	TGATCCTCCCACCTC[-/A]AGCCTCCTCAGTAGC	4703
rs35904965	in-del	-/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151533171	TACTGAAAAGTATAA[-/G]ATTAATGTTATACCA	4703
rs35913032	in-del	-/GA	0.444533	0.157025	intron-variant	NEB	GRCh38.p7	2:151730616	GGCTCATTTCTTAGT[-/GA]AAAAAAAAAAAAAAA	4703
rs35926277	in-del	-/T			intron-variant	NEB	GRCh38.p7	2:151660624	GATTGGCAAACTTTT[-/T]CTGTATAGACAGAAA	4703
rs35929034	in-del	-/C			intron-variant	NEB	GRCh38.p7	2:151630578	TGTAATATTTAACCC[-/C]AGAGATGAAAGGTTG	4703
rs35933372	in-del	-/A			intron-variant	NEB	GRCh38.p7	2:151535118	TAAATTTAACTTAAA[-/A]TTATTGCAAAGATGG	4703
rs35943488	snp	C/T	0.00438332	0.0466095	intron-variant	NEB, RIF1	GRCh38.p7	2:151530176	ATGAACTGATGAATA[C/T]AGCAATCATTCTGCC	4703
rs35946547	snp	C/T	0.000182629	0.00955411	synonymous-codon	NEB	GRCh38.p7	2:151663599	CTACAACATGCTTCC[C/T]GATGCCATGAGCTTT	4703
rs35967764	in-del	-/G			intron-variant	NEB	GRCh38.p7	2:151628026	GGCAGTAGTCTAATG[-/G]CGAAGTCTCATAAAT	4703
rs35974308	snp	A/G	0.0460646	0.144604	NEB	2	allele_origin=G(germline)/A(germline)	2:151642629	AAGGTTATGACATGC[A/G]GGTAGATGCCATTCC	4703
rs35994301	in-del	-/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151505024	TTTTTGGACACTGGG[-/G]AATCCTATCATTCAT	4703
rs36019698	in-del	-/G			intron-variant	NEB	GRCh38.p7	2:151726593	CAAATTAGACCCATT[-/G]GAAATGTGTCTGAAT	4703
rs36084429	in-del	-/C			intron-variant	NEB	GRCh38.p7	2:151714064	TCTTTCTACATAAAG[-/C]ACCAGACAGACCCAC	4703
rs36101756	in-del	-/T			intron-variant, utr-variant-3-prime	NEB, RIF1	GRCh38.p7	2:151497782	TTTCTTGGGACTTTT[-/T]AAGGATGAGGAAAAA	4703
rs36105240	snp	A/G	0.00695946	0.0585772	missense	NEB	GRCh38.p7	2:151710447	CCAGAATGAATGCTG[A/G]TAACATTAGCACAGT	4703
rs36182904	in-del	-/G			intron-variant	NEB	GRCh38.p7	2:151717342	TCAGTCTCACCTTTA[-/G]TAACCCTCTCTGATG	4703
rs41270201	snp	A/G	0.0478942	0.14715	NEB, RIF1	2	allele_origin=G(germline)/A(germline)	2:151508075	ACAGTCTCATAATAC[A/G]ACATGGACTTCTCAG	4703
rs41525550	snp	C/T	0.00354735	0.0419653	intron-variant	NEB, RIF1	GRCh38.p7	2:151527448	CTCAGGTGCAGTATG[C/T]AGTTACAATCGTCTG	4703
rs55636832	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151731441	GTTCTTCTCTGTTTT[C/T]TGCATATTTTTAAAG	4703
rs55641952	snp	A/G	0.161596	0.233848	intron-variant	NEB	GRCh38.p7	2:151704559	GCAGGATATAATCTC[A/G]TGGTGCGCCGTTTTT	4703
rs55680824	snp	A/G	0.00795532	0.062565	intron-variant	NEB	GRCh38.p7	2:151714025	ATTAAAGGCCCTTAG[A/G]GATTAATGGAAGCTA	4703
rs55720586	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151646988	GTGAAGGATTAGGAT[C/T]CCCAAAAGGATTTTT	4703
rs55817374	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151647552	TAACCAAGTGTTTAA[A/G]TTATTAGTAATAGAA	4703
rs55846441	snp	C/G	0.345925	0.230864	intron-variant	NEB	GRCh38.p7	2:151561484	CTGCCAGAATGAATA[C/G]CTTCTCTTGACTGAG	4703
rs55894710	snp	A/G	0.49706	0.0382258	intron-variant	NEB	GRCh38.p7	2:151620347	TATATGTATGTGTGT[A/G]TATATATATATATAT	4703
rs55914727	snp	A/G	0.00557542	0.0525036	intron-variant	NEB	GRCh38.p7	2:151543223	AATTTAATGTAATGC[A/G]GCAAATGAGAAAGAA	4703
rs55917454	snp	C/T	0.354235	0.227234	intron-variant	NEB	GRCh38.p7	2:151634755	ATTATTTTACTAGAT[C/T]CATGCATTCAATGGC	4703
rs55945158	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151668656	ATTTTGTGAAGAAAA[C/T]TAAACTTTTTTGGAT	4703
rs55945937	snp	C/G	0.16911	0.236552	intron-variant	NEB	GRCh38.p7	2:151642185	TGAACTTTGAGTAAT[C/G]TGTCCTATAATTCAG	4703
rs55996489	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151686771	TATACACAATATATA[A/C]TATAATTTGCAGTAG	4703
rs56002721	snp	C/T	0.406468	0.194981	intron-variant	NEB	GRCh38.p7	2:151574661	CTTATCATTTTAATG[C/T]AATGCTGAATTTGAT	4703
rs56026241	in-del	-/T	0.478167	0.102175	intron-variant	NEB, RIF1	GRCh38.p7	2:151531902	TGTATTTGATCTAAA[-/T]TGTGGAAGAGAAGAA	4703
rs56080930	snp	A/C	0.395635	0.2032	intron-variant	NEB, RIF1	GRCh38.p7	2:151494933	GATTACAGGCGTGAG[A/C]CACCACACCTGGCCC	4703
rs56214532	snp	C/T	0.00398564	0.0444627	intron-variant	NEB	GRCh38.p7	2:151706245	AGAAAAGATAACTAA[C/T]CCACACAGACAGCTA	4703
rs56224718	snp	C/T	0.416708	0.186302	intron-variant	NEB	GRCh38.p7	2:151556292	CAGAATGGAAATTAT[C/T]AGAGTGCACTGTCTC	4703
rs56240091	in-del	-/ATAT/ATATAT			intron-variant	NEB	GRCh38.p7	2:151620392	TATATATATATATAT[-/ATAT/ATATAT]TTAACCAGAATTTAA	4703
rs56258194	snp	C/T	0.342358	0.232314	intron-variant	NEB	GRCh38.p7	2:151632919	TCTTTTTGGAAAGAA[C/T]TGCAAAACACAGGGT	4703
rs56319152	snp	C/T	0.0260105	0.111035	intron-variant	NEB	GRCh38.p7	2:151573706	AGTTTCAAGCCTTGG[C/T]AAATTGCACTAAGGT	4703
rs56333529	in-del	-/CAAAA			intron-variant	NEB	GRCh38.p7	2:151698064	CAAAACAAAACAAAA[-/CAAAA]AGAAAAAAACCTGAC	4703
rs56343608	snp	A/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151515976	GTTAAAAATGACCAA[A/G]AGAAAATTTAGTGCT	4703
rs56401060	snp	G/T	0.139564	0.224285	intron-variant	NEB	GRCh38.p7	2:151550188	GGGAGGATCACTTGA[G/T]CCCAGGAATTTGAGA	4703
rs56805351	snp	C/G	0.0349115	0.127424	intron-variant	NEB, RIF1	GRCh38.p7	2:151508171	ATAGGCCAATGGGAC[C/G]TAAAATAGGCTATTT	4703
rs56963141	snp	C/G	0.00874735	0.0655527	intron-variant	NEB, RIF1	GRCh38.p7	2:151495006	CTCTCATAGACATAT[C/G]AGTAAAACTGTAGGC	4703
rs56974166	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151652238	TTAAAGAATTTTTTT[A/T]TTTTTGAGATACCGT	4703
rs56980395	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151652239	TAAAGAATTTTTTTA[A/T]TTTTGAGATACCGTC	4703
rs57057802	in-del	-/AA			intron-variant	NEB	GRCh38.p7	2:151550289	AAAAAAAAAAAAAAA[-/AA]CACTAATTCCTCTGT	4703
rs57082978	snp	A/T	0.341685	0.232581	intron-variant	NEB	GRCh38.p7	2:151623622	TGGATTATTAAGATG[A/T]GTCAGTTTATAGTCT	4703
rs57165100	in-del	-/A			intron-variant	NEB	GRCh38.p7	2:151635726	AAAAAAAAAAAAAAA[-/A]GAGTGTAACCTTAGG	4703
rs57312023	snp	C/T	0.0103295	0.0711199	intron-variant	NEB	GRCh38.p7	2:151716614	ATCTACAATATAAAA[C/T]ACTAATAAACATCAC	4703
rs57832702	in-del	-/AT/TA			intron-variant	NEB, RIF1	GRCh38.p7	2:151494390	TAGATGGAAAGTAGT[-/AT/TA]ATGTTTCCTAAGGAA	4703
rs57867185	in-del	-/AAA/AAAA			intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151498899	AGGTGCTAAAAAAAA[-/AAA/AAAA]GAAACTTCAAAATAT	4703
rs57965576	snp	C/T	0.0103295	0.0711199	intron-variant	NEB	GRCh38.p7	2:151560322	TACTTCTGACTCTAG[C/T]AGAGATTATCATGTG	4703
rs58037758	snp	C/G	0.407845	0.193868	intron-variant	NEB	GRCh38.p7	2:151574196	AGGCAGGATGGTCTC[C/G]ATCTCCTGACCTCGT	4703
rs58135483	snp	C/T	0.229136	0.249128	intron-variant	NEB	GRCh38.p7	2:151619396	ACTAGTCAGAACTCA[C/T]AGACACGTTTCAGAT	4703
rs58263509	snp	C/T	0.000880071	0.0209586	synonymous-codon	NEB	GRCh38.p7	2:151568651	ACTTTGTTTCGCTGT[C/T]ACATAATCAACTCTG	4703
rs58308258	in-del	-/GA/GACA			intron-variant	NEB, RIF1	GRCh38.p7	2:151500424	GAGTTGTATATAATA[-/GA/GACA]CACAAATAATTTGTG	4703
rs58354762	in-del	-/A			intron-variant	NEB	GRCh38.p7	2:151647973	TCTTATTCTTGGGAA[-/A]TACAGACGGAATATT	4703
rs58510460	in-del	-/AAAA	0.150667	0.229419	intron-variant	NEB, RIF1	GRCh38.p7	2:151520866	AAGACCCTGTCTCAC[-/AAAA]TAAATAAGAGGATTT	4703
rs58532073	snp	C/T	0.0376037	0.131863	intron-variant	NEB	GRCh38.p7	2:151637439	GAGTTGGACTGTGAA[C/T]GCCTCATTCTAAGAA	4703
rs58860557	snp	A/G	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151559734	TCGTAAGTGGGGGTT[A/G]AACAGTGAGAACACA	4703
rs58903550	snp	A/G	0.447032	0.153878	intron-variant	NEB	GRCh38.p7	2:151668957	CCCTACAATTCTCAG[A/G]GCAAGAGTTGCAAAG	4703
rs58909595	snp	C/T	0.344815	0.231323	intron-variant	NEB	GRCh38.p7	2:151610214	ATGGACAAGATTTTA[C/T]ATTACAAACATTTTG	4703
rs58993993	in-del	-/T	0	0	intron-variant	NEB	GRCh38.p7	2:151680386	GATTTTTTTTTTTTT[-/T]GCACTGACTTAAAAT	4703
rs58996775	snp	C/T	0.341685	0.232581	intron-variant	NEB	GRCh38.p7	2:151623632	AGATGTGTCAGTTTA[C/T]AGTCTTTTCAAGATG	4703
rs59037518	in-del	-/AT			intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151498633	CCGTGAAAGAGCAAT[-/AT]TAGTCTTTTCCCACC	4703
rs59290272	snp	A/G	0.0146672	0.084371	intron-variant	NEB, RIF1	GRCh38.p7	2:151495011	ATAGACATATCAGTA[A/G]AACTGTAGGCCCTCA	4703
rs59427070	in-del	-/A/AA			intron-variant	NEB	GRCh38.p7	2:151555885	TAAAAAAAAAAAAAA[-/A/AA]CACATACACACACAC	4703
rs59444636	snp	A/C	0.338523	0.233803	intron-variant	NEB	GRCh38.p7	2:151670161	AAAAAGAATTGACAC[A/C]AGTTATTACTCCTAA	4703
rs59493296	snp	C/T	0.265727	0.249505	intron-variant	NEB	GRCh38.p7	2:151641030	TGCATGGGTTTTATA[C/T]GCTCAATGATCCAAA	4703
rs59509952	in-del	-/CT	0.0569829	0.158885	utr-variant-3-prime, intron-variant	NEB, RIF1	GRCh38.p7	2:151485495	GCATATTCAAAATCC[-/CT]GTTTTAGAAAAGAAA	4703
rs59532113	snp	C/T	0.0138799	0.0821421	intron-variant	NEB	GRCh38.p7	2:151661904	TAAAAGAAAAAGTCC[C/T]TATTTATTTGGTTAT	4703
rs59607184	snp	A/C	0.0130921	0.0798413	intron-variant	NEB	GRCh38.p7	2:151732418	TGTGTTAGATGTCCA[A/C]TAATAATTGGAAGGA	4703
rs59619867	snp	C/T	0.0494327	0.149241	intron-variant	NEB	GRCh38.p7	2:151681619	TCGAAAACAAAACAC[C/T]GAACAAGAAGTAAAA	4703
rs59655785	snp	A/G	0.398354	0.201224	intron-variant	NEB	GRCh38.p7	2:151637704	GCTAGACACAGGGGG[A/G]GCCCTTTGTTTCCTG	4703
rs59681554	snp	A/T	0.0130921	0.0798413	intron-variant	NEB	GRCh38.p7	2:151732419	GTGTTAGATGTCCAC[A/T]AATAATTGGAAGGAA	4703
rs59723161	snp	C/T	0.331179	0.236453	intron-variant	NEB	GRCh38.p7	2:151573059	CGTGAATTTGCTTTG[C/T]TACCCATAAAATCAC	4703
rs59898635	in-del	-/A	0.46875	0.121031	intron-variant	NEB	GRCh38.p7	2:151556779	AGACTTTAACACCTC[-/A]CTGTCGACACTAGAC	4703
rs59941666	in-del	-/TCTCAGAATGAGACATACAGACGTG			intron-variant	NEB	GRCh38.p7	2:151670463	AGACATACAGACGTG[-/TCTCAGAATGAGACATACAGACGTG]GTATGAGTCCACGGT	4703
rs60069721	in-del	-/TT			intron-variant	NEB, RIF1	GRCh38.p7	2:151524683	TTTTTTTTTTTTTTT[-/TT]GAGATGGAATCTCAC	4703
rs60169474	in-del	-/AAA	0	0	intron-variant	NEB	GRCh38.p7	2:151719905	AAAAAAAAAAAAAAA[-/AAA]TACAAACTGAAGACT	4703
rs60202285	in-del	-/GA			intron-variant	NEB, RIF1	GRCh38.p7	2:151500426	GTTGTATATAATACA[-/GA]CAAATAATTTGTGTG	4703
rs60317553	in-del	-/GGA			intron-variant	NEB	GRCh38.p7	2:151707525	CAAGTAGGAGGAGGA[-/GGA]TGGAGCAGGGAGAAG	4703
rs60597794	snp	A/G	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151706494	CTTTTAAGTTCTGTT[A/G]TTGGCAAATGATGGT	4703
rs60629492	snp	C/T	0.0123036	0.0774623	intron-variant	NEB	GRCh38.p7	2:151691720	AATTGTTGTGTTCCC[C/T]GGTTCCACCCCAAAA	4703
rs60806638	snp	C/G	0.499999	0.000599041	intron-variant	NEB, RIF1	GRCh38.p7	2:151531714	AGTCTCCCAGACTTT[C/G]TGACAATTTAAAATG	4703
rs61014963	snp	C/T	0.00301197	0.0386899	intron-variant	NEB	GRCh38.p7	2:151562067	CACCACCATGGATTC[C/T]GATGACCCATGGAGA	4703
rs61027211	in-del	-/T			intron-variant	NEB	GRCh38.p7	2:151713274	TACCCTTCTCTTTTT[-/T]CTGTGAGGGGCTAAG	4703
rs61104725	snp	A/G	0.00597247	0.0543191	intron-variant	NEB	GRCh38.p7	2:151667115	TGGAAATAGAAATAC[A/G]AAAAACCAGAAAGAA	4703
rs61122586	in-del	-/GGGT			intron-variant	NEB, RIF1	GRCh38.p7	2:151491058	TTTTTTTTTGAGATG[-/GGGT]GGGTCTCTGTTGCTC	4703
rs61254943	snp	A/G	0.388587	0.208071	intron-variant	NEB	GRCh38.p7	2:151576372	GAAAAAGAAAACACA[A/G]GTAGAAGCAGGGTTT	4703
rs61576710	snp	C/T	0.0577344	0.159793	intron-variant	NEB	GRCh38.p7	2:151727163	GTTCCAGTGTGCAGC[C/T]ATGGTTAATAACCAC	4703
rs61730765	snp	C/T	0.0515527	0.152048	NEB, RIF1	2	allele_origin=T(germline)/C(germline)	2:151526245	TCTTTCCTTGACATG[C/T]TTCTCTTTGTATTTC	4703
rs61730769	snp	A/G	0.0259695	0.110952	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151491772	GTACGCCAGACACGT[A/G]AACCTGAAAGGGAAA	4703
rs61730771	snp	A/C/G	0.0423692	0.13925	NEB	2	allele_origin=G(germline)/A(germline)	2:151640574	CTGGATCTTGGCCAC[A/C/G]TGCATGGACCACATC	4703
rs61730780	snp	C/T	0.0539897	0.155177	missense, intron-variant	NEB	GRCh38.p7	2:151650297	ATGATTTCCGAAGCC[C/T]GCTTGTTCTTTTCTG	4703
rs62167160	snp	G/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151502777	ATTTTTTTTTTTTTG[G/T]CCCCCTAAGAAATAC	4703
rs62167161	snp	C/T	0.0070493	0.0589488	intron-variant	NEB, RIF1	GRCh38.p7	2:151502930	CATTTAAAACAGGCA[C/T]AGAGAGTAAGGAAGG	4703
rs62167162	snp	C/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151529083	TTGTTCATGCTCCTG[C/G]GGCCTGACTCTTGCT	4703
rs62167164	snp	C/G	0.0180037	0.0931542	NEB	2	allele_origin=G(germline)/C(germline)	2:151537930	GGACGATCAGGAATG[C/G]ACCTCCAGATACCCA	4703
rs62174683	snp	A/G	0.0134861	0.0810011	intron-variant	NEB	GRCh38.p7	2:151563751	ACATTGAGAATCGCT[A/G]GAGTTTCCTAACCAG	4703
rs62174688	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151578396	GGACATTCTTCTGTT[C/T]AAGAAACTGCCCCAG	4703
rs62174689	snp	C/G	0.425894	0.177655	intron-variant	NEB	GRCh38.p7	2:151579326	GACTTGTTTCCTGGG[C/G]GACACACTTACGTCG	4703
rs62174690	snp	G/T	0.451108	0.148512	missense, intron-variant	NEB	GRCh38.p7	2:151579498	ACAGGGATGGAGATC[G/T]TGGCTTTGTGGTCGT	4703
rs62174691	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151584825	CTGCCTCAGACTCCT[A/G]AGTAGCTGGGATTAC	4703
rs62174692	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151587992	TTGTGATCATAAGTT[A/G]AAGTCGTGAGTGCTA	4703
rs62174693	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151588788	TGAACTCATTCATTA[C/T]AAAAAGGTATCTCTG	4703
rs62174694	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151588794	CATTCATTACAAAAA[A/G]GTATCTCTGGAAGCT	4703
rs62174695	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151588798	CATTACAAAAAGGTA[C/T]CTCTGGAAGCTTAAG	4703
rs62174696	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151588823	CTTAAGGGAACCAAG[A/G]TCAGATAATTTTTAA	4703
rs62174697	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151588889	GTAATCCATCATTTC[C/T]AAAAGTCTGAAGGGC	4703
rs62174698	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151588896	ATCATTTCTAAAAGT[C/T]TGAAGGGCAGAAAAT	4703
rs62174699	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151588905	AAAAGTCTGAAGGGC[A/G]GAAAATACGAGTAAA	4703
rs62174700	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151589074	GGACATTCTTCTGTT[C/T]AAGAAACTGCCCCAG	4703
rs62174701	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151598431	AAAGATTGTATGAGA[A/G]GCAAGGTGCAGGCTT	4703
rs62174702	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151598445	AGGCAAGGTGCAGGC[C/T]TTCAGCACTGAAACT	4703
rs62174703	snp	C/T	0.5	0	intron-variant	NEB	GRCh38.p7	2:151604121	TAACATCAGTTGGAT[C/T]TTAGGAGGTAAAGAA	4703
rs62174704	snp	C/T	0.5	0	intron-variant	NEB	GRCh38.p7	2:151604281	GAAATATGTATATGA[C/T]TATGCAAAGGTAACG	4703
rs62174706	snp	A/C			synonymous-codon, intron-variant	NEB	GRCh38.p7	2:151612312	TTCTCCAGCTCTCTT[A/C]ACTTTCTCGACCTCT	4703
rs62174707	snp	C/T	0.318656	0.240388	intron-variant	NEB	GRCh38.p7	2:151615903	TAAAGGGAATTGAGA[C/T]TTATAGGGGTAACTA	4703
rs62174709	snp	A/G	0.317692	0.240661	intron-variant	NEB	GRCh38.p7	2:151620371	TATATATATATATAT[A/G]TATATATATATATAT	4703
rs62174710	snp	A/G	0.5	0	intron-variant	NEB	GRCh38.p7	2:151620375	TATATATATATATAT[A/G]TATATATATATATAT	4703
rs62174711	snp	A/G	0.5	0	intron-variant	NEB	GRCh38.p7	2:151620377	TATATATATATATAT[A/G]TATATATATATATAT	4703
rs62174712	snp	A/G	0.5	0	intron-variant	NEB	GRCh38.p7	2:151620379	TATATATATATATAT[A/G]TATATATATATATTT	4703
rs62174727	snp	C/T	0.0103295	0.0711199	intron-variant	NEB	GRCh38.p7	2:151637146	TGATGGAGAGACTGA[C/T]AACCTGTGGAAGCAA	4703
rs62174728	snp	C/G	0.461923	0.132621	intron-variant	NEB	GRCh38.p7	2:151638809	TATTTCTCTCTCTCT[C/G]TGTGTGTGTGTGTGT	4703
rs62174729	snp	A/G	0.0217236	0.101931	intron-variant	NEB	GRCh38.p7	2:151657508	GGTGTAAATATGCCC[A/G]TCACAGCTGATATCA	4703
rs62174730	snp	A/C	0.5	0	intron-variant	NEB	GRCh38.p7	2:151692246	TACCCGAAAGGTAAC[A/C]GTGGCTTTTCGAACC	4703
rs62174731	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151699454	CTGACTTCCACAATG[C/G]TTGAACTAGTTTACA	4703
rs62174732	snp	C/G			intron-variant	NEB	GRCh38.p7	2:151699737	CTTGTAAATTTGTTT[C/G]AGTTCATTGTAGATT	4703
rs62174733	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151699765	ATTCTGGATATTAGC[C/T]CTTTGTCAGATGAGT	4703
rs62174756	snp	A/T	0.0174175	0.0916809	intron-variant	NEB	GRCh38.p7	2:151732698	GTTACCCTATAGATG[A/T]TTAGCTAGTTGAAGC	4703
rs66468516	snp	C/T	0.192715	0.243348	intron-variant	NEB	GRCh38.p7	2:151640873	TATATACCATATAGA[C/T]AGGCATTACTTTAAT	4703
rs66541369	in-del	-/A	0.480461	0.0968913	intron-variant	NEB	GRCh38.p7	2:151540212	TTTTTTTTTCTCTTT[-/A]AAAAAAATGTGTGTT	4703
rs66881625	in-del	-/AAAA			intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151498892	AGGTGCTAAAAAAAA[-/AAAA]GAAACTTCAAAATAT	4703
rs67239108	in-del	-/TTT	0.181022	0.240296	intron-variant	NEB	GRCh38.p7	2:151658177	TACCACTGTGGCGTC[-/TTT]TTTTTTTGTTTTTGA	4703
rs67476200	in-del	-/TG			intron-variant	NEB	GRCh38.p7	2:151723749	TCTACCTGCCTTCTT[-/TG]TTTTTTTTTTTTTTT	4703
rs67484661	snp	A/T	0	0	intron-variant	NEB	GRCh38.p7	2:151698880	CTTTTTTTTTTTTTT[A/T]AATTATACTTTAAGT	4703
rs67996056	in-del	-/A			intron-variant	NEB	GRCh38.p7	2:151556780	GACTTTAACACCTCC[-/A]TGTCGACACTAGACA	4703
rs71000480	in-del	-/TTT	0	0	intron-variant	NEB	GRCh38.p7	2:151576550	TTTTTTTTTTTTTTT[-/TTT]TTTTTTTTTTGAGAC	4703
rs71000481	in-del	-/AT	0	0	intron-variant	NEB	GRCh38.p7	2:151620391	TATATATATATATAT[-/AT]TTAACCAGAATTTAA	4703
rs71000485	in-del	-/GT	0	0	intron-variant	NEB	GRCh38.p7	2:151723750	CTACCTGCCTTCTTT[-/GT]TTTTTTTTTTTTTTT	4703
rs71350102	snp	G/T	0.0205511	0.0992634	intron-variant	NEB, RIF1	GRCh38.p7	2:151510645	AGTATATTGTTATAA[G/T]TGTTCTATTTTATTA	4703
rs71350303	snp	C/G	0.373196	0.217538	intron-variant	NEB	GRCh38.p7	2:151698669	TTGAGATGGAGTCTC[C/G]CTCTGTTGCCCAGGC	4703
rs71357322	snp	G/T	0	0	intron-variant	NEB	GRCh38.p7	2:151704232	TCTCAGATCTCCAGC[G/T]GCGTGCTGGGAGAAC	4703
rs71392958	snp	A/G	0.5	0	intron-variant	NEB	GRCh38.p7	2:151605023	CAGTTCACTTTAAAG[A/G]AATTAGATAATACGA	4703
rs71403173	in-del	-/T	0.5	0	intron-variant	NEB, RIF1	GRCh38.p7	2:151512019	GTTACCCTCTCACTC[-/T]TTTTTTTTTTTTTTT	4703
rs71415141	snp	C/T	0.00438332	0.0466095	intron-variant	NEB, RIF1	GRCh38.p7	2:151523258	ATAAAATATGTTACA[C/T]AGGAATTTTAAGTTT	4703
rs71415142	snp	C/T	0.5	0	intron-variant	NEB	GRCh38.p7	2:151551680	CAAGCTCAGCTTGCT[C/T]CCACAGAGGCTGATG	4703
rs71415143	snp	G/T	0.5	0	intron-variant	NEB	GRCh38.p7	2:151578695	AAGGAAGGAAGGAAG[G/T]AGAGAAGGAGGGAAG	4703
rs71415144	snp	G/T	0.5	0	intron-variant	NEB	GRCh38.p7	2:151578697	GGAAGGAAGGAAGGA[G/T]AGAAGGAGGGAAGGA	4703
rs71415145	snp	G/T	0.5	0	intron-variant	NEB	GRCh38.p7	2:151578723	AAGGAAGGAAGGAAG[G/T]AGGGAAGGAAGGAAG	4703
rs71415146	snp	G/T	0.5	0	intron-variant	NEB	GRCh38.p7	2:151578743	AAGGAAGGAAGGAAG[G/T]AGAGAAGGAAGGAAC	4703
rs71415157	snp	C/T	0.5	0	intron-variant	NEB	GRCh38.p7	2:151594788	ATCTCCATCACCAAG[C/T]TTCCCTGACAAGTGC	4703
rs71415158	snp	C/T	0.0295035	0.117819	intron-variant	NEB	GRCh38.p7	2:151605440	GGTTTTGGAAACAGA[C/T]AAGAAAGATGCATGT	4703
rs71415160	snp	C/T	0.444444	0.157135	intron-variant	NEB	GRCh38.p7	2:151605587	TTTCCTATGTTTGGA[C/T]AACATAGGCAAGTTT	4703
rs71415168	snp	A/T	0.5	0	intron-variant	NEB	GRCh38.p7	2:151607327	GATGTATCCAAGCAC[A/T]CATTTAAAAGAGAGA	4703
rs71415169	snp	G/T	0.5	0	intron-variant	NEB	GRCh38.p7	2:151668053	AGGACTATTAGTTTG[G/T]CTTTTATGTATATAA	4703
rs71415170	snp	G/T	0.5	0	intron-variant	NEB	GRCh38.p7	2:151676627	ACTGCTGTTATATTG[G/T]TCATTCCTTTTCTAC	4703
rs71415171	snp	G/T	0.5	0	intron-variant	NEB	GRCh38.p7	2:151676648	CCTTTTCTACTGCTG[G/T]TATATTGTTCCTTTT	4703
rs71415174	snp	C/T	0.0310518	0.120672	intron-variant	NEB	GRCh38.p7	2:151718291	AGGGAGACTCTGAAC[C/T]CCAGCACTTAGCTTG	4703
rs71415175	snp	A/C	0.5	0	intron-variant	NEB	GRCh38.p7	2:151732389	TAAAATAAATGATTA[A/C]CAGCTTTGTAAAATG	4703
rs71415176	snp	G/T	0.5	0	upstream-variant-2KB	NEB	GRCh38.p7	2:151735928	CTTTAAAATGTGTTG[G/T]TGAATTAAAAAATAA	4703
rs71996133	in-del	-/TGTG			intron-variant	NEB	GRCh38.p7	2:151638808	ATATTTCTCTCTCTC[-/TGTG]TGTGTGTGTGTGTGT	4703
rs72071424	in-del	-/TG			intron-variant	NEB	GRCh38.p7	2:151638808	ATATTTCTCTCTCTC[-/TG]TGTGTGTGTGTGTGT	4703
rs72120958	in-del	-/G	0.348794	0.229651	intron-variant	NEB	GRCh38.p7	2:151609202	ATTTCAAAATAAAAG[-/G]AAAAAAAAAAGGAAA	4703
rs72227806	in-del	-/TGTGTG			intron-variant	NEB	GRCh38.p7	2:151638808	ATATTTCTCTCTCTC[-/TGTGTG]TGTGTGTGTGTGTGT	4703
rs72621644	snp	A/G	0.00597247	0.0543191	intron-variant	NEB	GRCh38.p7	2:151641095	TTCTAGATAAGTACC[A/G]CAGATTCAATAAAAA	4703
rs72861620	snp	A/G			intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151507078	TTCTTTATTTGTCCT[A/G]TATTATGTGAAGAAA	4703
rs72863249	snp	A/G	0.5	0	intron-variant	NEB	GRCh38.p7	2:151609204	ATTTCAAAATAAAAG[A/G]AAAAAAAAAGGAAAA	4703
rs72863259	snp	A/G	0.00755907	0.0610114	intron-variant	NEB	GRCh38.p7	2:151620414	AGAATTTAAACATTT[A/G]AAAACCTATAAAAAT	4703
rs72863267	snp	A/C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151626445	TTGCTCTGTGCTTAC[A/C/T]TAAATAAGTACTCAG	4703
rs72863268	snp	C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151627904	CTCATTAATTTAAAA[C/T]TTTATTATTTTAAAA	4703
rs72863280	snp	C/T	0.00478085	0.0486577	intron-variant	NEB	GRCh38.p7	2:151667016	TATTATGTCAATTCA[C/T]ATAGGAATATAACTT	4703
rs72863283	snp	A/C	0.235564	0.249583	intron-variant	NEB	GRCh38.p7	2:151676710	GGAAACTCTGGTAGG[A/C]AGTTACCTGTGTACA	4703
rs72863291	snp	A/G	0.00716266	0.059414	intron-variant	NEB	GRCh38.p7	2:151705014	TCTTTCCTCACTGAT[A/G]GCACCACAGCAAACA	4703
rs73005907	snp	A/G	0.142609	0.225759	intron-variant	NEB, RIF1	GRCh38.p7	2:151486656	TATCCATACAGATCT[A/G]TTATTGGGTAGTAAC	4703
rs73005916	snp	A/G	0.00199481	0.0315187	intron-variant	NEB, RIF1	GRCh38.p7	2:151495693	CAACAAACAAAAAAC[A/G]AAAACTGGTAAAACA	4703
rs73005917	snp	A/G	0.128632	0.218563	intron-variant	NEB, RIF1	GRCh38.p7	2:151496636	CATTTTTGTGAGTAC[A/G]GTGCCTCCTAAACAA	4703
rs73005979	snp	A/G	0.0107246	0.0724382	intron-variant	NEB, RIF1	GRCh38.p7	2:151504741	GCGTATGGATGGGAA[A/G]AGGGGTGGGTGCAGA	4703
rs73005996	snp	G/T	0.110872	0.20771	intron-variant	NEB	GRCh38.p7	2:151544101	CTTGGATCAGCATTT[G/T]ATCAAGCCTGGGTCA	4703
rs73007903	snp	C/T	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151547942	AAGCCTTCCACTTTC[C/T]ATCAGATGGTTGCAT	4703
rs73007929	snp	A/G	0.00835141	0.0640778	intron-variant	NEB	GRCh38.p7	2:151628155	GAAGCAACACTTTCC[A/G]GAAGATCTTTCGGTA	4703
rs73007940	snp	C/T	0.337386	0.23423	intron-variant	NEB	GRCh38.p7	2:151648673	TCCCTGGCTTCTACC[C/T]ACTAGATGCCAGTAG	4703
rs73007946	snp	A/G/T	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151685152	TCCCCCAAAAAGCAC[A/G/T]CATGGGCAGACCTTC	4703
rs73007948	snp	A/G	0.00318978	0.0398085	intron-variant	NEB	GRCh38.p7	2:151685633	AACGTTGGCCCTTCC[A/G]TACAGCATTATAAAC	4703
rs73007953	snp	G/T	0.0123036	0.0774623	intron-variant	NEB	GRCh38.p7	2:151688700	TGTGATAAAGTTTAA[G/T]TTATATATTAGGCAC	4703
rs73007959	snp	G/T	0.0123036	0.0774623	intron-variant	NEB	GRCh38.p7	2:151696789	CTGTCAGATCCAAGG[G/T]GGCCCACAGGCCAAG	4703
rs73007985	snp	C/G	0.0123036	0.0774623	intron-variant	NEB	GRCh38.p7	2:151722534	GTTTAGTTGTTGTTG[C/G]TGTGGTCATTGTTTG	4703
rs73007989	snp	A/G	2.50529e-05	0.00353919	synonymous-codon	NEB	GRCh38.p7	2:151723433	CAGTTCCGGGCTATC[A/G]TTATAGGGGTAAAAC	4703
rs73009858	snp	G/T	0.0023933	0.0345097	upstream-variant-2KB	NEB	GRCh38.p7	2:151735841	GTCTTATGACCAAAG[G/T]ATATTTATGTAATAT	4703
rs73967561	snp	C/G	0.180064	0.240019	intron-variant	NEB	GRCh38.p7	2:151547067	GGCAGCAAGAAGTTG[C/G]TAATGAGGTCAGAGT	4703
rs73967562	snp	A/C	0.133777	0.221342	intron-variant	NEB	GRCh38.p7	2:151549479	ATCAATTGCACAGCA[A/C]CCCTCAAAAATATGC	4703
rs73967566	snp	A/G	0.147656	0.228091	intron-variant	NEB	GRCh38.p7	2:151567949	ACCATCACCAAGCCT[A/G]GCCAGGTCTGCCACA	4703
rs73967567	snp	C/T	0.00256265	0.0357037	missense	NEB	GRCh38.p7	2:151568168	CTCTCCCAGCCTTCC[C/T]TGTAGAGATACTGAA	4703
rs73967569	snp	C/T	0.144296	0.226554	intron-variant	NEB	GRCh38.p7	2:151573874	TTTTTTTTTCCTCAG[C/T]TGATTCTCTTTTTTA	4703
rs73967575	snp	A/T	0.188946	0.24243	intron-variant	NEB	GRCh38.p7	2:151615704	CTCAATTATTTATTT[A/T]TTTTTTTTGAAGACG	4703
rs73967578	snp	G/T	0.223225	0.248562	intron-variant	NEB	GRCh38.p7	2:151632179	TTTTTTTTTGCTGAA[G/T]GTTTTTATATACCCA	4703
rs73967579	snp	A/G	0.0520825	0.152737	intron-variant	NEB	GRCh38.p7	2:151632810	CAGAGAAGGTGCCCA[A/G]CAAATAGACAGATGG	4703
rs73967581	snp	C/T	0.228842	0.249103	intron-variant	NEB	GRCh38.p7	2:151634178	ACCCCAAATCACCTA[C/T]AGCCTGGTACTAAGG	4703
rs73967584	snp	C/T	0.046775	0.145601	intron-variant	NEB	GRCh38.p7	2:151681871	ATAATTCTTCAAAGA[C/T]GATTTCTATAATAAC	4703
rs73967586	snp	C/T	0.0244538	0.107838	intron-variant	NEB	GRCh38.p7	2:151690965	TATATTCTCACTTCT[C/T]TGTCTGTCTCTCTCT	4703
rs73967589	snp	C/T	0.00636936	0.0560724	intron-variant	NEB	GRCh38.p7	2:151724716	CATCTGTGCAGCCTC[C/T]TTGATGAATACAGGT	4703
rs74320183	snp	A/G	0.00087736	0.0209263	synonymous-codon	NEB	GRCh38.p7	2:151677700	CTTTTTAACTTTTTC[A/G]ACGTCGAGACTGCCA	4703
rs74328528	snp	C/T	0.0322114	0.122752	intron-variant	NEB	GRCh38.p7	2:151628027	GGCAGTAGTCTAATG[C/T]GAAGTCTCATAAATA	4703
rs74357123	snp	A/G	0.136506	0.222754	intron-variant	NEB	GRCh38.p7	2:151652319	AAGCCTCAGCCTTCC[A/G]AGCTCAAGTGATCCT	4703
rs74391169	snp	C/T	0.0217236	0.101931	upstream-variant-2KB	NEB	GRCh38.p7	2:151735506	TCTTTCTCTGGGTTG[C/T]TCCTGTATTCAGGCA	4703
rs74429765	snp	C/T	0.0372196	0.131242	intron-variant	NEB, RIF1	GRCh38.p7	2:151530414	GGCTTTTTCATTAAT[C/T]GTTGGGGAAGGATCC	4703
rs74435646	snp	C/T	0.0341408	0.126114	intron-variant	NEB	GRCh38.p7	2:151717248	TAACACAGTTCTTGA[C/T]GTTTATGGATGTATT	4703
rs74473884	snp	C/T	0.00716266	0.059414	intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151507143	CACAATAATTATGGT[C/T]TGGTAGCCCAAGGGA	4703
rs74482326	snp	C/T	0.000960153	0.0218896	missense	NEB	GRCh38.p7	2:151671063	TGAGCCAACACCATG[C/T]CCATGGAATCAGGCA	4703
rs74486389	snp	A/G	0.0193772	0.0965046	intron-variant	NEB	GRCh38.p7	2:151615492	TTGTTCTTGTGTCCG[A/G]TGAGGGACATCTCAC	4703
rs74527227	snp	C/G	0.21303	0.247251	intron-variant	NEB	GRCh38.p7	2:151691363	GCCCATCCAGTCACT[C/G]TCTCACACATTGTCC	4703
rs74532673	snp	C/T	0.186737	0.241863	intron-variant	NEB	GRCh38.p7	2:151694213	CTTTCATGTGTGATT[C/T]GTCATCTTGAATCCA	4703
rs74548340	snp	C/G	0.0524604	0.153226	upstream-variant-2KB	NEB	GRCh38.p7	2:151735258	AGAGCAGATAACATG[C/G]AAATCAGTAACTTAT	4703
rs74586903	snp	G/T	0.48	0.0979796	intron-variant	NEB	GRCh38.p7	2:151723751	TACCTGCCTTCTTTG[G/T]TTTTTTTTTTTTTTT	4703
rs74622558	snp	C/T	0.00398564	0.0444627	intron-variant	NEB	GRCh38.p7	2:151616409	AAAATTATTTACTGG[C/T]CGGGCGTGGTGGCTC	4703
rs74626643	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151654209	ATCGAACATCATCTA[A/C]CCTATCTTTAAAGAT	4703
rs74630432	snp	G/T	0.0130921	0.0798413	intron-variant	NEB	GRCh38.p7	2:151637426	TGAGAATAGCCCAGA[G/T]TTGGACTGTGAACGC	4703
rs74684819	snp	A/T	0.0490535	0.14873	intron-variant	NEB	GRCh38.p7	2:151562878	ATCAATGTCTTTTAG[A/T]TCCTTATTTCCCATA	4703
rs74692049	snp	A/G	0.00557542	0.0525036	intron-variant	NEB	GRCh38.p7	2:151720407	CTGACAACAGTATTA[A/G]TAGGCATGTCAATAA	4703
rs74747513	snp	C/T	0.0494327	0.149241	intron-variant	NEB	GRCh38.p7	2:151696857	GTAGTTAATAAAATA[C/T]ATTTTTTTCTAACTA	4703
rs74751445	snp	C/T	0.0260105	0.111035	intron-variant	NEB, RIF1	GRCh38.p7	2:151511348	TAATCAAACCACTCT[C/T]TAGTGATAACTATAT	4703
rs74756840	snp	A/G	0.5	0	intron-variant	NEB	GRCh38.p7	2:151689829	TATTAAGATGCTCAG[A/G]AAAGTGGCACACGAG	4703
rs74774971	snp	C/T	0.00415965	0.045415	intron-variant	NEB	GRCh38.p7	2:151667766	GAACTCCTGAAGTCT[C/T]TTAGATAGAAAGTTT	4703
rs74780321	in-del	-/AAA			intron-variant	NEB	GRCh38.p7	2:151546016	TAAAAAAAAAAAAAA[-/AAA]CAGAAATACAAGTTG	4703
rs74802483	snp	A/C/T	0.0287284	0.116357	intron-variant	NEB	GRCh38.p7	2:151716942	TATAGGTAGACTAAG[A/C/T]TGTTTGTTAGGGCCT	4703
rs74804252	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151631893	TTTGGATTCTTATTC[C/T]CTGCGATGTATTCTT	4703
rs74813400	snp	A/G	0.0263992	0.111815	intron-variant	NEB	GRCh38.p7	2:151730120	TTTTAAATGGATTGC[A/G]TCATGGAAATAATAA	4703
rs74814103	snp	A/G	0.5	0	intron-variant	NEB	GRCh38.p7	2:151668290	TAATGAAGCATTTCA[A/G]GCTTATAGGAAGATA	4703
rs74820105	snp	A/G	0.153665	0.230694	intron-variant	NEB, RIF1	GRCh38.p7	2:151526548	CCATAAGCCCTCCAT[A/G]AGCCCATTATTATTC	4703
rs74829016	snp	A/G	0.0123036	0.0774623	intron-variant	NEB	GRCh38.p7	2:151647901	TCTGTAGACTAGCAG[A/G]CCAGTGGAAATTAAT	4703
rs74831611	snp	C/T	0.0919752	0.193722	intron-variant	NEB	GRCh38.p7	2:151647918	CAGTGGAAATTAATT[C/T]TGTGATTTTAATCAT	4703
rs74859201	snp	A/C/T	0.0310078	0.120594	NEB	2	allele_origin=T(germline)/C(germline)	2:151679913	CCGTGAGTCCACCCA[A/C/T]GCACCTCACTGATAT	4703
rs74885771	snp	A/T	0.5	0	intron-variant	NEB	GRCh38.p7	2:151625374	CTTTCTATCTGCCTA[A/T]TTTTTAATACAATAA	4703
rs74886039	snp	A/T	0.00597247	0.0543191	intron-variant	NEB, RIF1	GRCh38.p7	2:151489207	GACAGTTGTCTTCAT[A/T]CAAAGATTGTTCATA	4703
rs74916574	snp	A/G	0.5	0	intron-variant	NEB	GRCh38.p7	2:151540323	CCATCACAACAGAAG[A/G]AAAAAGGAAGGGATG	4703
rs74935217	snp	A/G	0.040671	0.13668	intron-variant	NEB	GRCh38.p7	2:151657001	TCCTTTTCCTTTAAG[A/G]CTCTCTAAACTGCTA	4703
rs74942276	snp	C/T	0.0520825	0.152737	intron-variant	NEB	GRCh38.p7	2:151654838	CAAGTCTGTTTGATG[C/T]AATTTTTACTTTATT	4703
rs74954359	in-del	-/AACA			intron-variant	NEB, RIF1	GRCh38.p7	2:151509328	GATGTAAGGAAAACA[-/AACA]GTTCTCATTGTCCTG	4703
rs74956359	snp	C/T	0.00874735	0.0655527	intron-variant	NEB	GRCh38.p7	2:151719465	TCTAACTGTATCTTA[C/T]CCCAATAATATCTAC	4703
rs74999312	snp	G/T	0.00358779	0.0422022	intron-variant	NEB	GRCh38.p7	2:151571397	GGCTTTGTTTTCTTG[G/T]GTTGGTGTATTGGTA	4703
rs75003522	snp	A/T	0.00636936	0.0560724	intron-variant	NEB	GRCh38.p7	2:151613030	AACTGGTTGAAGGAA[A/T]ATTTTTCTTGTAAGG	4703
rs75005333	snp	A/G	0.0603597	0.1629	intron-variant	NEB	GRCh38.p7	2:151643703	TGGGTGACTAGATGC[A/G]CTTGGGCATTAGTCC	4703
rs75048674	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151676379	TTTCGGTGACAGCCT[A/T]CTAATTCATCTTCTC	4703
rs75073923	snp	A/C	0.168723	0.236419	missense	NEB	GRCh38.p7	2:151682720	AAGGACCCAAAAGGC[A/C]CCCAGCCACAACCTT	4703
rs75118047	snp	A/C	0.0154199	0.0864419	NEB	2	allele_origin=A(germline)/C(germline)	2:151694638	AAAGATTCTGGACAA[A/C]AAAATTCAGCAAAGG	4703
rs75127853	snp	C/T	0.0611083	0.163768	intron-variant	NEB	GRCh38.p7	2:151721920	GTGGAAGGATACGAC[C/T]GTATCTGTGTTATAT	4703
rs75162551	snp	A/G	0.0520825	0.152737	intron-variant	NEB	GRCh38.p7	2:151653055	TTAAGTGAATTAAAT[A/G]AAATCTTCCCCTATA	4703
rs75170780	snp	A/G	0.0314385	0.121371	intron-variant	NEB	GRCh38.p7	2:151715713	TGTGAGAAAATAAAC[A/G]TCTATTGTTTAAGCC	4703
rs75221580	snp	A/G	0.00109942	0.0234201	intron-variant	NEB, RIF1	GRCh38.p7	2:151513564	TGAAAGATTGACATC[A/G]AATAGTAGCACTGAC	4703
rs75244176	snp	A/G	0.133777	0.221342	intron-variant	NEB	GRCh38.p7	2:151685971	CATATTTTGTGGGTG[A/G]TCATTTTCACTGAAT	4703
rs75254271	snp	C/T	0.0349115	0.127424	intron-variant	NEB	GRCh38.p7	2:151731864	TTTCTGACCCTTAGG[C/T]ACATAAGTAAAATGC	4703
rs75260990	snp	A/C/G	0.0295035	0.117819	intron-variant	NEB	GRCh38.p7	2:151644901	ACTTATGCAATCCTA[A/C/G]ATGGTACGGCCTAGT	4703
rs75266729	snp	G/T	0	0	intron-variant	NEB	GRCh38.p7	2:151717870	CTTTTTTTTTTTTTT[G/T]TGAGACGGAGTCTCA	4703
rs75272311	snp	A/T	0.0225045	0.103662	intron-variant	NEB	GRCh38.p7	2:151731510	TTTTTCGAATGCACC[A/T]CCCTCTTATGCTCAT	4703
rs75291571	snp	A/G	0.0209421	0.100162	intron-variant	NEB	GRCh38.p7	2:151654440	ATTTTGAAGATAGAT[A/G]TTAAGATAATTGCTA	4703
rs75299359	snp	C/T	0.0528381	0.153711	intron-variant	NEB	GRCh38.p7	2:151674070	AAAAAGTGGACTTTT[C/T]CCTCTTTGGTTTATA	4703
rs75300348	snp	C/T	0.0197687	0.0974348	intron-variant	NEB	GRCh38.p7	2:151618619	ACTCACTCACGCACA[C/T]TATTGAATCCTAAGT	4703
rs75320668	snp	A/G/T	0.00210596	0.0323816	intron-variant	NEB	GRCh38.p7	2:151697531	CAGAAAGAGTGACAG[A/G/T]AGGATTGCTTACATC	4703
rs75323975	snp	A/C	0.00755907	0.0610114	intron-variant	NEB, RIF1	GRCh38.p7	2:151528845	CATCAGAAGAAGCAG[A/C]TTGTAGAGTTTGAGG	4703
rs75333635	snp	G/T			missense	NEB	GRCh38.p7	2:151725532	TATGGCTGTCCTTTT[G/T]TTTTCTCAAACTTCT	4703
rs75346830	snp	A/G	0.0532157	0.154195	intron-variant	NEB	GRCh38.p7	2:151722126	AATCAGTCTGAACTG[A/G]CTTACTAAGTCCAAA	4703
rs75396628	snp	A/G	0.171057	0.237209	intron-variant	NEB	GRCh38.p7	2:151698624	TTGTACCCTGTATCA[A/G]TACTTCATTAATTTT	4703
rs75410226	snp	A/G	0.0448719	0.142907	intron-variant	NEB	GRCh38.p7	2:151696795	GATCCAAGGTGGCCC[A/G]CAGGCCAAGCAAATA	4703
rs75414727	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151562525	GAATACAGGGACAAC[A/G]GGAGCATGGCAGCCA	4703
rs75418704	snp	C/T	0.0498117	0.149749	intron-variant	NEB, RIF1	GRCh38.p7	2:151523387	ATATCTTCCAAAAGA[C/T]TGGAATCCCATGTTT	4703
rs75470740	snp	A/G/T	4.35571e-05	0.00466658	intron-variant	NEB	GRCh38.p7	2:151612434	AGATGTCACCTAGAC[A/G/T]GCCTGGTGCCTGATC	4703
rs75471310	snp	G/T	0	0	intron-variant	NEB, RIF1	GRCh38.p7	2:151502775	GGATTTTTTTTTTTT[G/T]GGCCCCCTAAGAAAT	4703
rs75506805	snp	C/T	0.00358779	0.0422022	intron-variant	NEB	GRCh38.p7	2:151661876	AAACAGGACTCATTT[C/T]CAAGAGGTGCAGTAA	4703
rs75513863	snp	C/T	0.00119737	0.0244387	intron-variant	NEB, RIF1	GRCh38.p7	2:151523944	TTAGAATTTCATTGC[C/T]CTTCATGTTAAATCT	4703
rs75514769	snp	A/C/T	0.0058947	0.05397	intron-variant	NEB	GRCh38.p7	2:151710560	AAAAGAAAAAGAAAA[A/C/T]AAGACAAGCATAACT	4703
rs75515097	snp	G/T	0.000927576	0.0215157	intron-variant	NEB, RIF1	GRCh38.p7	2:151527468	ACAATCGTCTGTGTC[G/T]CTCCTGTCTTACATC	4703
rs75518052	snp	C/T	0.5	0	intron-variant	NEB	GRCh38.p7	2:151717856	ATACCTCCTTTGTTC[C/T]TTTTTTTTTTTTTTT	4703
rs75549502	snp	A/C/T	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151486567	ATGTCCGTAGCAGCA[A/C/T]TACTCATAATAGCCA	4703
rs75572293	snp	C/T	0.0829062	0.185956	intron-variant	NEB	GRCh38.p7	2:151575101	AATTGCAATGGATTT[C/T]CTTCTTTTACTAGGC	4703
rs75630911	snp	C/T	0.0240643	0.107019	intron-variant	NEB	GRCh38.p7	2:151685136	TACATACCATTGAAA[C/T]TCCCCCAAAAAGCAC	4703
rs75639119	snp	C/T	0.00691599	0.0583966	missense, intron-variant	NEB	GRCh38.p7	2:151627801	CTCCAATGTGGTGGC[C/T]GAGCTGCTTGCGGTA	4703
rs75643374	snp	C/T	0.000798403	0.0199641	intron-variant	NEB	GRCh38.p7	2:151734222	GACTCTAATCACACA[C/T]GGTACATAGCAGATA	4703
rs75648481	snp	A/G	0.0456336	0.143994	intron-variant	NEB	GRCh38.p7	2:151663989	GGAAGGGAGGCACTC[A/G]TGAGAGGGAGGGAGC	4703
rs75665029	snp	C/T	0.0279526	0.114869	upstream-variant-2KB	NEB	GRCh38.p7	2:151735090	AATCCTATTTAGCAC[C/T]TTCTCCCTCCTTAGA	4703
rs75684310	snp	A/T	0.021333	0.101051	intron-variant	NEB	GRCh38.p7	2:151659293	AGGTTTAAATTAATT[A/T]ATTTATTTATTTATT	4703
rs75687497	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151528419	AAATTTCAAACATAC[A/G]AAAATGTTGCAAGAA	4703
rs75702091	snp	C/T	0.0448719	0.142907	intron-variant	NEB	GRCh38.p7	2:151676908	TAATACAGTGCCTGG[C/T]ACATGGTAAATGTTC	4703
rs75722587	snp	A/C	0.00358779	0.0422022	intron-variant	NEB	GRCh38.p7	2:151669816	GTTTTAAGACAGGCT[A/C]TTGCGATTGTTTGAG	4703
rs75795281	snp	A/C	0.5	0	intron-variant	NEB	GRCh38.p7	2:151622707	AGATATTTTTATATA[A/C]TGACAGTATATGTAT	4703
rs75797633	snp	A/G	0.0829062	0.185956	intron-variant	NEB, RIF1	GRCh38.p7	2:151495905	CAAAAACACAACAAA[A/G]TCATATTTAAGAAAG	4703
rs75804242	snp	A/G	0.00240172	0.0345701	intron-variant	NEB	GRCh38.p7	2:151548261	TTCAAACAAAGCCAT[A/G]GCTATTGAAACTCAA	4703
rs75805078	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151654212	GAACATCATCTACCC[A/T]ATCTTTAAAGATATG	4703
rs75807392	snp	A/G	0.142798	0.225849	NEB	2	allele_origin=G(germline)/A(germline)	2:151659169	CTTGTTTGTAGAGAT[A/G]CTAGGAAAAAAACAG	4703
rs75830808	snp	C/T	0.0236746	0.106192	intron-variant	NEB	GRCh38.p7	2:151656691	ACTCTCCTCATTTTA[C/T]AGATGAATAAGCTGA	4703
rs75832634	snp	A/T	0.0310518	0.120672	intron-variant	NEB	GRCh38.p7	2:151734272	GCAATGGGGTTAAAC[A/T]CTCCTAGCCATATTT	4703
rs75843358	snp	A/G	0.5	0	intron-variant	NEB	GRCh38.p7	2:151661113	GCTGTTCTTTTCTCA[A/G]CTCTGCAATGGGAGG	4703
rs75859017	snp	C/T	0.0341408	0.126114	intron-variant	NEB	GRCh38.p7	2:151691280	GTTCTTCCCTGCTGC[C/T]GTTCCCCTGACCTTG	4703
rs75873810	snp	A/T			splice-acceptor-variant	NEB	GRCh38.p7	2:151568419	TTCCGGTATTTAATC[A/T]AAAAAAAAAAAAATG	4703
rs75880964	snp	C/G	0.00755907	0.0610114	intron-variant	NEB	GRCh38.p7	2:151706547	TGAAAGTCTCCTTCT[C/G]CTTCTGTCAAAATCA	4703
rs75883373	snp	G/T	0.0494327	0.149241	intron-variant	NEB	GRCh38.p7	2:151693245	GAGTTTTATCTTATT[G/T]TTTATTTTTTTGTTT	4703
rs75895266	snp	A/G	0.0150606	0.0854603	intron-variant	NEB	GRCh38.p7	2:151709398	GGAAATATTGAAGAT[A/G]GTAATTAGATGTTAT	4703
rs75901530	snp	A/G	0.0479149	0.147179	intron-variant	NEB	GRCh38.p7	2:151705347	TAAATGATGCTATTC[A/G]TGTTTAATATTTTTA	4703
rs75907947	snp	C/T	0.00716266	0.059414	intron-variant	NEB	GRCh38.p7	2:151609679	ATTAAACAATGTGAA[C/T]GGTACCCCCAGCCCC	4703
rs75908937	snp	C/T	0.00874735	0.0655527	intron-variant	NEB	GRCh38.p7	2:151637220	AGGAGTCATTTATTC[C/T]GAACTGAGAATCAGG	4703
rs75931010	snp	C/T	0.0170251	0.090679	intron-variant	NEB, RIF1	GRCh38.p7	2:151526508	CTTACGTTCACAGCA[C/T]GCTCAGATATGCCAT	4703
rs75944430	snp	C/G	0.0584853	0.160693	intron-variant	NEB	GRCh38.p7	2:151713229	ATTTTTATGTGGTTA[C/G]CAAATGGAAAGGAAT	4703
rs75983376	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151578006	ATCACTACTTCCACA[A/G]TTTTGGTCTCCAGAA	4703
rs75995378	snp	A/T	0.039522	0.134904	intron-variant	NEB	GRCh38.p7	2:151651797	TTACATATATAAAAT[A/T]TTCAGGAGTTTAAGT	4703
rs76016277	snp	A/T	0.0952156	0.196321	intron-variant	NEB	GRCh38.p7	2:151654486	GGTCACAACATTTTA[A/T]TTAGCTAAGTGATAA	4703
rs76047035	snp	A/G/T	0.125182	0.216612	intron-variant	NEB	GRCh38.p7	2:151722471	CTGAAGTATCTTCTG[A/G/T]TAGCAAGAGCTCTTT	4703
rs76123095	snp	C/T	0.0391387	0.134304	intron-variant	NEB, RIF1	GRCh38.p7	2:151514714	AACCCAATTTGAAAC[C/T]CACAGTTAGGTGGTG	4703
rs76127015	snp	C/T	0.0142366	0.0831603	intron-variant	NEB	GRCh38.p7	2:151696599	TATGAAATGTTATCC[C/T]TCATAATTGGGTGTC	4703
rs76128511	snp	C/T	0.00874735	0.0655527	intron-variant	NEB	GRCh38.p7	2:151706416	ATGCTTTAAATTGAA[C/T]GGCTTAGTCGGGCTC	4703
rs76129073	snp	A/G	0.0236746	0.106192	intron-variant	NEB	GRCh38.p7	2:151667388	TCTTCTAACAACTTT[A/G]TTAAGCTTTTAAATA	4703
rs76153088	snp	A/G	0.5	0	intron-variant	NEB	GRCh38.p7	2:151553530	GATAGAAAGGATCAG[A/G]AAAAAAAAATTGACC	4703
rs76177996	snp	C/T	0.121717	0.214577	intron-variant	NEB	GRCh38.p7	2:151726410	AGTGAGCTGCTATCA[C/T]TTAATGAAAAGTGAG	4703
rs76204433	snp	A/G	0.00874735	0.0655527	intron-variant	NEB	GRCh38.p7	2:151712583	TCACAATCCACTCCC[A/G]AGCACTGCCAAGTCT	4703
rs76213967	snp	C/T	0.5	0	intron-variant	NEB	GRCh38.p7	2:151615136	ATCTACCTTGAAGAT[C/T]CCAGAATAACGCATT	4703
rs76244655	snp	A/T	0.021333	0.101051	intron-variant	NEB	GRCh38.p7	2:151671542	GCATTTTTTTTCAAG[A/T]CACTTACTGTATTAT	4703
rs76252750	snp	C/T	0.0448719	0.142907	intron-variant	NEB	GRCh38.p7	2:151729926	TTAATCAAGAGAAGC[C/T]ATTTTACTTTACTGG	4703
rs76255313	snp	C/T	0.5	0	intron-variant	NEB, RIF1	GRCh38.p7	2:151530785	GGCTTGACTGAGCCC[C/T]AGGTGTCTGCCAGCA	4703
rs76255773	snp	A/G	0.0410537	0.137264	intron-variant	NEB	GRCh38.p7	2:151629922	ATAGATCAATATGAT[A/G]TACATATCAGCATAG	4703
rs76261031	snp	G/T	0.0429047	0.140041	intron-variant	NEB	GRCh38.p7	2:151560958	TTACTGTCCCAGAAG[G/T]GGGAAAGGTGGCTCA	4703
rs76262827	snp	A/G	0.0912534	0.193131	intron-variant	NEB, RIF1	GRCh38.p7	2:151515280	CTTAAGGTGACAAAA[A/G]ACTTTATTTCAGAAT	4703
rs76264092	snp	A/G	0.0433465	0.140692	intron-variant	NEB	GRCh38.p7	2:151646503	ATTACATGCCTTGCC[A/G]ATATTATCAAATGAA	4703
rs76287069	snp	C/G	0.0225045	0.103662	intron-variant	NEB	GRCh38.p7	2:151685409	ATACACAGGGCTGTA[C/G]ACTTAGTTTATTGGC	4703
rs76314607	snp	A/G	0.00318978	0.0398085	intron-variant	NEB	GRCh38.p7	2:151679263	AAATTCTTAACTGTA[A/G]TAGAACCCAAAGACT	4703
rs76321692	snp	A/C	0.0689305	0.172377	intron-variant	NEB	GRCh38.p7	2:151620708	CTATTGAGCAAAGAT[A/C]AAAAATAAGGAGTCA	4703
rs76346927	snp	C/T	0.116838	0.211584	intron-variant	NEB, RIF1	GRCh38.p7	2:151486812	GGTAGCCAAATAATA[C/T]AGTGACAGGAAATGG	4703
rs76375465	snp	C/G	0.0584853	0.160693	intron-variant	NEB	GRCh38.p7	2:151706698	CCACAGAACCACAAA[C/G]AGTAAGGCACATTGT	4703
rs76400407	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151717388	CAGAGTCTTCAAGGG[A/C]GGCAATGTCCCAGCT	4703
rs76488145	snp	C/T	0.0513262	0.151752	intron-variant	NEB	GRCh38.p7	2:151672152	GTTTTATCTTTTATC[C/T]ATAAGTTAATAAAGA	4703
rs76498020	snp	C/T	0.0103295	0.0711199	intron-variant	NEB, RIF1	GRCh38.p7	2:151502521	CTGTGTTACACCAGT[C/T]AGAAACACCTACTGT	4703
rs76504462	snp	C/T	0.0240643	0.107019	intron-variant	NEB	GRCh38.p7	2:151722165	AAGAGGTTCCAGGGA[C/T]CTAACTGACAATTGA	4703
rs76523290	snp	C/G/T	5.44394e-05	0.00521701	intron-variant	NEB	GRCh38.p7	2:151619402	CAGAACTCACAGACA[C/G/T]GTTTCAGATCCGCTT	4703
rs76545410	snp	A/T	0.5	0	intron-variant	NEB	GRCh38.p7	2:151664022	ACTCTTTTTACTTCA[A/T]TTTTTTTTTTCCCGA	4703
rs76550036	snp	C/T	0.0341408	0.126114	intron-variant	NEB	GRCh38.p7	2:151689108	CTGCTAGGTTGTGTC[C/T]GGAGAACACGAACTT	4703
rs76559186	snp	C/T	0.0588605	0.161139	intron-variant	NEB	GRCh38.p7	2:151731030	GAAAATATTGTTTGA[C/T]GCTGACGCCACATAG	4703
rs76591052	snp	A/G	1.90188e-05	0.00308367	intron-variant	NEB, RIF1	GRCh38.p7	2:151502895	CAAAACCTGTGAGAT[A/G]CAAGAAAGTACCCAG	4703
rs76594381	snp	C/G	0.0162398	0.0886349	intron-variant	NEB	GRCh38.p7	2:151564810	CATTGAGCTTTAGCC[C/G]CTCATTGCCTCCTAA	4703
rs76613929	in-del	-/AA			intron-variant	NEB	GRCh38.p7	2:151729077	CACCTTGAAAAAAAA[-/AA]GAGCTTGAACGTGGA	4703
rs76662961	snp	A/T	0	0	intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151497282	GAGTTATCCATGTTA[A/T]TTTTTTTTTTCCTTT	4703
rs76664802	snp	G/T	0.00146534	0.0270282	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151526226	GTACGGCATGGCAGG[G/T]TCCTCTTTCCTTGAC	4703
rs76673047	snp	C/G	0.00478085	0.0486577	intron-variant	NEB	GRCh38.p7	2:151645866	GCCTGTCCACACTGG[C/G]AAGAGCAATATAAGC	4703
rs76673906	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151534621	ATGGCATCTAACGGT[A/G]TATTTAAAATAGGGT	4703
rs76697324	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151661050	ATCCCTGTTCTAGTC[A/C]AGACCCTGCTGTTGA	4703
rs76737405	snp	C/T	0.0448719	0.142907	intron-variant	NEB	GRCh38.p7	2:151690341	TGTTACTGTGCCCTT[C/T]CTTTTTGCAAAATCT	4703
rs76767949	snp	A/C/T	0.0197857	0.0974765	NEB	2	allele_origin=T(germline)/C(germline)	2:151642841	TGGACAGTGGTTTTA[A/C/T]CTTTATCCCAAGCTT	4703
rs76787276	snp	A/G	0.0209421	0.100162	intron-variant	NEB, RIF1	GRCh38.p7	2:151488998	AGTATTATCATTTTC[A/G]AATTTTACTTGATTA	4703
rs76790417	snp	A/T	0.0839998	0.186933	intron-variant	NEB	GRCh38.p7	2:151561608	GAACACTTTTTTTTT[A/T]TTATTATTATACTTT	4703
rs76810008	snp	C/T	0.117537	0.212022	intron-variant	NEB, RIF1	GRCh38.p7	2:151488081	CCTTTTTCTGTTGGC[C/T]ATTTATATTTATTTT	4703
rs76819780	snp	C/T	0.077417	0.180873	intron-variant	NEB	GRCh38.p7	2:151682305	ATTTATTAAAACTTG[C/T]CAAAGTGTACACTTA	4703
rs76855426	snp	C/T	0.0168055	0.0901129	intron-variant	NEB	GRCh38.p7	2:151542315	TCTCCCGGGGTGATC[C/T]CATCTGTACCTGTGA	4703
rs76860735	snp	C/T	0.00199481	0.0315187	intron-variant	NEB	GRCh38.p7	2:151638725	TCTATGATTCTGGAA[C/T]GATGGCACGTGGCCC	4703
rs76926856	snp	C/T	0.0490535	0.14873	intron-variant	NEB	GRCh38.p7	2:151685994	CACTGAATACATTTA[C/T]TATTTAACTATAAAA	4703
rs76935557	snp	A/G	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151686892	ATTCAGGCAAAAGGC[A/G]TGAAAAGAAATGTTC	4703
rs77027033	snp	C/G	0.0154538	0.0865337	intron-variant	NEB, RIF1	GRCh38.p7	2:151490287	AAAATTTTTAAATTT[C/G]TTTTTGTACTCAAAG	4703
rs77028362	snp	A/G	0.00318978	0.0398085	intron-variant	NEB	GRCh38.p7	2:151611272	TCTTGAGAAAGGTAC[A/G]TAACTCCTCACATTC	4703
rs77044468	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151647472	ATATCTCCCTGCCAG[A/T]TTACTTATCAATTAC	4703
rs77054491	snp	A/G	0.00557542	0.0525036	intron-variant	NEB	GRCh38.p7	2:151629441	TAGAAAAACAAGCCA[A/G]TAAATGTGCTTAAAC	4703
rs77062531	snp	G/T	0.0626037	0.165477	intron-variant	NEB	GRCh38.p7	2:151645203	GATTATTATTGAGGT[G/T]CTGTTTTTCAATTCA	4703
rs77080541	snp	A/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151503623	CCAAAATAGTAAAAA[A/T]TTTTACTACTTTGAA	4703
rs77083451	snp	G/T	0	0	intron-variant	NEB	GRCh38.p7	2:151647127	ATAATTTTTTTTTTT[G/T]GAGATGGAGTTTCAC	4703
rs77091895	snp	A/G	0.00953873	0.0683987	intron-variant	NEB	GRCh38.p7	2:151707935	CACTTTTCCACCTTA[A/G]AGAATTAACTGTTTC	4703
rs77149626	snp	A/G	0.0341408	0.126114	intron-variant	NEB	GRCh38.p7	2:151687915	TCTCCCTACCACTAA[A/G]TAAGTATCAACTACT	4703
rs77151072	snp	C/T	0.0104695	0.0715899	missense	NEB	GRCh38.p7	2:151688389	TCATGTTTTGCTTTG[C/T]AATTCAGCTGAAAAA	4703
rs77154348	snp	A/T	0.0130921	0.0798413	intron-variant	NEB	GRCh38.p7	2:151690539	TTATTTTTATTATTG[A/T]CTAACACAACTTTCC	4703
rs77171268	snp	A/C	0.5	0	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151529242	AGGCGTCCTTGGCTG[A/C]TTTGATATGAACAGC	4703
rs77233070	snp	A/G	0.398354	0.201224	intron-variant	NEB	GRCh38.p7	2:151559963	ACAAAACACACACAC[A/G]CAAAAAGGTTTTACT	4703
rs77236877	snp	A/G	0.0103295	0.0711199	intron-variant	NEB	GRCh38.p7	2:151685719	GTTAGACAAGGTGCT[A/G]GTTGGGTCAAATTCC	4703
rs77239448	snp	C/T	0.0916144	0.193427	intron-variant	NEB, RIF1	GRCh38.p7	2:151508592	AGCCATGAGCAGGTG[C/T]GGTCAGGGCTCCCAG	4703
rs77270718	snp	A/G	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151721955	ACCAATTACATAGAA[A/G]GTGAAATAGAAAAAG	4703
rs77278257	snp	A/C	0.0399052	0.1355	intron-variant	NEB	GRCh38.p7	2:151721636	TCATACTTTTATTTT[A/C]TCAGCCTGATTATAA	4703
rs77279207	snp	A/G	0.039522	0.134904	intron-variant	NEB, RIF1	GRCh38.p7	2:151516393	GAAACTGGCCATGTC[A/G]TGGGCAGAGCTTGTG	4703
rs77385846	snp	A/G	0.00318978	0.0398085	intron-variant	NEB	GRCh38.p7	2:151695965	TCTGAGAGGGGCCCC[A/G]CCCTGTCTCTCTTGT	4703
rs77395793	snp	A/C	0	0	intron-variant	NEB	GRCh38.p7	2:151635709	AAAACTCTGTCTCCA[A/C]AAAAAAAAAAAAAAA	4703
rs77418991	snp	A/G/T	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151707517	TCAATTTACAAGTAG[A/G/T]AGGAGGAGGATGGAG	4703
rs77455721	snp	C/T	0.0225045	0.103662	intron-variant	NEB	GRCh38.p7	2:151683691	AATAGAGCTACCATG[C/T]GATCCAACTATTCAA	4703
rs77474850	snp	A/G			intron-variant	NEB	GRCh38.p7	2:151598435	ATTGTATGAGAGGCA[A/G]GGTGCAGGCTTTCAG	4703
rs77478656	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151660953	AATATGATTTATGTA[A/T]ATATAAATCAACACA	4703
rs77486954	snp	A/G	0.0295035	0.117819	intron-variant	NEB	GRCh38.p7	2:151718619	GCTCAGAGGAGAAAC[A/G]TCCTTCAGAGGGAAT	4703
rs77507435	snp	G/T	0.0566069	0.158427	intron-variant	NEB	GRCh38.p7	2:151649089	TTTTTATCTCCTGTT[G/T]CATGGAAAGAAAAGA	4703
rs77521841	in-del	-/G			intron-variant	NEB	GRCh38.p7	2:151722470	ACTGAAGTATCTTCT[-/G]ATAGCAAGAGCTCTT	4703
rs77534070	snp	A/G	0.111928	0.208413	intron-variant	NEB, RIF1	GRCh38.p7	2:151509427	GATTAAGCAAAAGCT[A/G]CCTCAACTGGTTTGC	4703
rs77538319	snp	A/G	0.00755907	0.0610114	intron-variant	NEB	GRCh38.p7	2:151724630	CAACAGCCTGGAGCC[A/G]AGTCACAGCTGCCTC	4703
rs77543961	snp	C/T	0.00241915	0.0346947	intron-variant	NEB	GRCh38.p7	2:151684738	CCATTTCAGTTTCCA[C/T]CTTTTTAAAAGAGGG	4703
rs77544031	snp	C/T	0.00279162	0.0372561	intron-variant	NEB	GRCh38.p7	2:151553196	TTCTCCACCAGAGGA[C/T]GATGGCACACCTGGA	4703
rs77547727	snp	A/G	0.0152607	0.0860086	NEB	2	allele_origin=G(germline)/A(germline)	2:151662333	AGCATAGTCAGCCTT[A/G]TACTGATTCTGCAAA	4703
rs77560924	snp	C/T	0.00874735	0.0655527	intron-variant	NEB	GRCh38.p7	2:151717632	CTAGATGTTACATAC[C/T]ATTGCTCTCAGTACT	4703
rs77567545	snp	C/G	0.0626037	0.165477	intron-variant	NEB	GRCh38.p7	2:151671511	GGTACTTTCTATAAT[C/G]GTTGTTTATCTTAAA	4703
rs77581064	snp	C/T	0.0314385	0.121371	intron-variant	NEB	GRCh38.p7	2:151718314	TTAGCTTGAAATCTA[C/T]ATGCCTGCCCAGTGG	4703
rs77609804	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151654211	CGAACATCATCTACC[C/T]TATCTTTAAAGATAT	4703
rs77622515	snp	A/G	0.0916144	0.193427	intron-variant	NEB, RIF1	GRCh38.p7	2:151508448	ATGCCTCCAGTGGCA[A/G]TAGTCCTCGCTGGGC	4703
rs77630398	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151507694	TTTATTGAATAAATT[A/G]TGTGTCTCTCTTGTT	4703
rs77632045	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151676380	TTCGGTGACAGCCTT[A/C]TAATTCATCTTCTCA	4703
rs77668847	snp	C/T	0.0341408	0.126114	intron-variant	NEB	GRCh38.p7	2:151733838	TGATTGAGGTACATA[C/T]AGGATTGTCAGTCCT	4703
rs77669964	snp	C/T	0.00636936	0.0560724	intron-variant	NEB	GRCh38.p7	2:151708683	TCAGGCTCATGTAGT[C/T]GACTGACCTCTGACA	4703
rs77674470	snp	A/G	0.00398564	0.0444627	intron-variant	NEB, RIF1	GRCh38.p7	2:151525472	CACCTGGCAATCTTC[A/G]GAGAACCTGGGTAGA	4703
rs77695696	snp	C/G	0.000798403	0.0199641	intron-variant	NEB, RIF1	GRCh38.p7	2:151503774	AAATATAGTAGGCCT[C/G]CAGTAGACTTGTACT	4703
rs77698187	snp	C/G	0.0154538	0.0865337	intron-variant	NEB	GRCh38.p7	2:151635398	ACAGTTTTGCTCTGG[C/G]AGACGTGCTAAATGG	4703
rs77728938	snp	C/T	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151653289	TATGCTAGCAATATG[C/T]AGAATATCTAAGTAA	4703
rs77732019	snp	A/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	NEB, RIF1	GRCh38.p7	2:151496814	CCAAAGGAAAAAAGG[A/T]TAAATTTGCTAAAGA	4703
rs77733926	snp	C/T	0.0333695	0.124785	intron-variant, nc-transcript-variant	NEB, RIF1	GRCh38.p7	2:151534061	CACTCAAATAGCTGA[C/T]GGGCTTTTTGGGTGG	4703
rs77734671	snp	C/T	0	0	upstream-variant-2KB	NEB	GRCh38.p7	2:151735738	ATGTACCTTTTCCCC[C/T]TCCATGATTCACATG	4703
rs77753093	snp	C/T	0.0193772	0.0965046	intron-variant	NEB	GRCh38.p7	2:151614678	GTTTCTTTTTCTTTT[C/T]CCCAACACTATCATG	4703
rs77785992	snp	A/T			intron-variant	NEB	GRCh38.p7	2:151676378	ATTTCGGTGACAGCC[A/T]TCTAATTCATCTTCT	4703
rs77826191	snp	A/T	0.00103447	0.0227193	missense	NEB	GRCh38.p7	2:151692360	GTTTTCCTTGTATAA[A/T]CTCTGTTAAAGGAAA	4703
rs77827516	snp	A/G	0.0138799	0.0821421	intron-variant	NEB	GRCh38.p7	2:151629244	CTCTATGCTCAAAAT[A/G]TGGAGATGAATTTCT	4703
rs77829631	snp	G/T			intron-variant	NEB	GRCh38.p7	2:151670760	TTTCATATGTATAAT[G/T]CGTATCTGCTTATGA	4703
rs77836537	snp	A/G	0.00358779	0.0422022	intron-variant	NEB	GRCh38.p7	2:151686819	GTAGTAAGAATTTTA[A/G]CTGCAAAATGTTACA	4703
rs77846253	snp	C/T	0.0147477	0.0845952	intron-variant	NEB	GRCh38.p7	2:151729679	TAGAGCACAAAGGCA[C/T]TGGCAAGAGAACCAA	4703
rs77875934	snp	A/G	0.0178098	0.0926698	intron-variant	NEB, RIF1	GRCh38.p7	2:151513413	GCAATGAGCCTGGCA[A/G]AGGGTCCTCCATCCT	4703
rs77884575	snp	A/G	0.140242	0.224618	intron-variant	NEB	GRCh38.p7	2:151568823	GAAACATACAGTGCC[A/G]TATTTGAATAGCGTC	4703
rs77888471	snp	C/T	0.00716266	0.059414	upstream-variant-2KB	NEB	GRCh38.p7	2:151736146	AATAATTCTATTGAT[C/T]GGATAGAGTATAATA	4703
rs77889129	snp	G/T	0.02016	0.0983543	intron-variant	NEB, RIF1	GRCh38.p7	2:151520167	TCTGTGAAATCCAAA[G/T]AAGGGCTGTAAATGA	4703
rs77907054	snp	A/G	0.031825	0.122064	intron-variant	NEB	GRCh38.p7	2:151713828	TTGGCCAAAGACAAA[A/G]GTGAGAGAATTGATT	4703
rs77954046	snp	A/T	0.104149	0.203046	intron-variant	NEB	GRCh38.p7	2:151637473	GGTGTTTAATTCTAC[A/T]GAAAATAGGAAAGCA	4703
rs77994592	snp	A/G	0.000398598	0.0141117	missense	NEB	GRCh38.p7	2:151727768	GATCCACTTTCTTCC[A/G]GATGACCTTCCTCCT	4703
rs78007533	snp	G/T	0.0352966	0.128072	intron-variant	NEB, RIF1	GRCh38.p7	2:151503736	AAATCTAACCATTTT[G/T]TTGCATCTAGCTTTG	4703
rs78062528	snp	C/T	0.0271762	0.113356	intron-variant	NEB, RIF1	GRCh38.p7	2:151532976	ATCAAAGTCAAGAGG[C/T]GCCATGAATATATAC	4703
rs78078428	snp	G/T	0.0372196	0.131242	intron-variant	NEB, RIF1	GRCh38.p7	2:151526834	AGCAGCTCTTCTCCA[G/T]CCTTCCCTGGTGTCC	4703
rs78085464	snp	C/T	0.0174175	0.0916809	intron-variant	NEB	GRCh38.p7	2:151693114	ATTTTGTAACACCTC[C/T]GGAAGCTGGCTATTA	4703
rs78128680	snp	A/G	0.0322114	0.122752	intron-variant	NEB	GRCh38.p7	2:151670367	CAGAACTCTAAAATT[A/G]ACAAGTCATGTGAGG	4703
rs78149441	snp	A/T	0.00159617	0.0282053	intron-variant	NEB	GRCh38.p7	2:151688727	GCACAGTAAGAGATT[A/T]ACAACAATAACTAAT	4703
rs78167444	snp	C/T	0.0221141	0.102801	intron-variant	NEB, RIF1	GRCh38.p7	2:151523510	GGTAGGATCTGTAAA[C/T]TGGAGGAGAAATGAG	4703
rs78168095	snp	C/G	0.0513262	0.151752	intron-variant	NEB	GRCh38.p7	2:151708188	CTACTGGATTCTTTC[C/G]ATCAACATGATGCTT	4703
rs78193127	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151519855	CACAAATGCCAAAGA[A/G]TATGCATTGTACATA	4703
rs78226234	snp	A/G/T	0.029724	0.118238	intron-variant	NEB	GRCh38.p7	2:151644443	ATTGCAATCAAATCA[A/G/T]TATCAACAGAGGATA	4703
rs78261389	snp	A/G	0.00478085	0.0486577	intron-variant	NEB	GRCh38.p7	2:151641628	GAGCCATGGTGCCTG[A/G]CCTATACACATGATT	4703
rs78262185	snp	A/C	0.5	0	intron-variant	NEB	GRCh38.p7	2:151635710	AAACTCTGTCTCCAA[A/C]AAAAAAAAAAAAAAA	4703
rs78276723	snp	C/T	0.00589306	0.0539611	intron-variant	NEB	GRCh38.p7	2:151639248	AACTGAAATAAGCAG[C/T]AGTGTGCAAATGTCA	4703
rs78292131	snp	C/T			intron-variant	NEB	GRCh38.p7	2:151658178	ACCACTGTGGCGTCT[C/T]TTTTTTTGTTTTTGA	4703
rs78299584	snp	G/T	0.0225045	0.103662	intron-variant	NEB	GRCh38.p7	2:151708179	CTTCCCTTTCTACTG[G/T]ATTCTTTCCATCAAC	4703
rs78333353	snp	C/T	0.5	0	intron-variant	NEB	GRCh38.p7	2:151734063	CAGGCAAATGAAGCC[C/T]AGTAGAACAGGATAA	4703
rs78353363	snp	A/G	0.000399281	0.0141238	intron-variant	NEB, RIF1	GRCh38.p7	2:151523850	CATCTGCTCATCCCT[A/G]CTTCCTAGCCCGGGC	4703
rs78362366	snp	A/G	0.031825	0.122064	intron-variant	NEB	GRCh38.p7	2:151725764	TGGTTGGATCTTGGA[A/G]ACAATGCAAATTTAT	4703
rs78414215	snp	A/G	0.0352966	0.128072	intron-variant	NEB, RIF1	GRCh38.p7	2:151515630	CAGTCTCCAGACTTA[A/G]CTGACTCACAGAGGG	4703
rs78415336	snp	A/C	0.0209421	0.100162	intron-variant	NEB	GRCh38.p7	2:151670359	CATTTTAACAGAACT[A/C]TAAAATTAACAAGTC	4703
rs78420579	snp	G/T	0.000376959	0.0137236	missense	NEB	GRCh38.p7	2:151664541	CTTGCAGCCTTTATT[G/T]CAATGGCATCAGGCC	4703
rs78427369	snp	C/T	0.0111196	0.0737302	intron-variant	NEB	GRCh38.p7	2:151613600	TATTATAGTTTGATA[C/T]AGTTTGGCTCTGCAT	4703
rs78430905	snp	A/G	0.0584853	0.160693	intron-variant	NEB	GRCh38.p7	2:151713759	TCTGACTGTTCATCT[A/G]TGTTAGAGCTACAAA	4703
rs78481438	snp	C/T	0.00119737	0.0244387	downstream-variant-500B, intron-variant	NEB, RIF1	GRCh38.p7	2:151484869	ACCCAGTGCCTGGCA[C/T]AGAGGTGTACGTTGG	4703
rs78482419	snp	C/T	0.202651	0.245475	intron-variant	NEB	GRCh38.p7	2:151656985	TTTATATTCGTGGAG[C/T]TCCTTTTCCTTTAAG	4703
rs78540635	snp	A/G	0.0513262	0.151752	intron-variant	NEB	GRCh38.p7	2:151673060	ATCACAAATATGAGT[A/G]CCAGCTATAGGATAG	4703
rs78555217	snp	A/T	0	0	intron-variant	NEB	GRCh38.p7	2:151676722	AGGCAGTTACCTGTG[A/T]ACAAGGCACCTCCCT	4703
rs78556634	snp	C/T	0.0558544	0.157504	intron-variant	NEB	GRCh38.p7	2:151612702	TCTGATTTGATGGTC[C/T]CTACCTCCTCTTATG	4703
rs78592085	snp	A/G	0.00352155	0.0418136	missense, intron-variant	NEB, RIF1	GRCh38.p7	2:151490008	GGGATGGAAGATACC[A/G]TTGTCTGTTGGGTAG	4703
rs78626031	snp	A/G	0.0584853	0.160693	upstream-variant-2KB	NEB	GRCh38.p7	2:151734873	AGGTGAGCTACAGGT[A/G]AGTTACTGGTGCTAG	4703
rs78626039	snp	A/G	0.0448719	0.142907	intron-variant	NEB	GRCh38.p7	2:151712698	AGAGAATTTGAAAGG[A/G]CAAGGGTCCATAGGT	4703
rs78690011	snp	C/T	0.00914312	0.0669923	intron-variant	NEB	GRCh38.p7	2:151659243	ATACATATCATTGTA[C/T]ATATATATCAATATT	4703
rs78711592	snp	A/G	0.0916144	0.193427	intron-variant	NEB, RIF1	GRCh38.p7	2:151504208	TAGTGCATGGCGTGG[A/G]GAGCAACGTACCCAG	4703
rs78713434	snp	C/G	0.00914312	0.0669923	intron-variant	NEB	GRCh38.p7	2:151622885	CAAGAGAATGAGTAG[C/G]ATTTAGTTCTCTAGT	4703
rs78721175	snp	C/T	0.0543475	0.155628	intron-variant	NEB	GRCh38.p7	2:151706170	CTTGCCACTTTCCCA[C/T]ACCTGCTCCCCAACC	4703
rs78733601	snp	A/C	0.0168187	0.090147	NEB	2	allele_origin=A(germline)/C(germline)	2:151655360	ATCTTTATTCCAATC[A/C]ATGGTGTATAAATGC	4703
rs78750194	snp	C/G			intron-variant	NEB, RIF1	GRCh38.p7	2:151517156	TGTTAAAAAACCTGA[C/G]AGTCTCAAAAGATCC	4703
rs78773099	snp	A/C	0.00676609	0.0577691	intron-variant	NEB, RIF1	GRCh38.p7	2:151533156	ATTTCTTTGAGGCAA[A/C]TACTGAAAAGTATAA	4703
rs78775134	snp	A/G	0.0119091	0.0762411	intron-variant	NEB	GRCh38.p7	2:151631481	TGTATAAGGCAAACT[A/G]AAAGAATTATGCTCA	4703
rs78775419	snp	G/T	0.00597247	0.0543191	intron-variant	NEB	GRCh38.p7	2:151641779	TATTCATAGACAAAA[G/T]AAATGGAAAGATAAA	4703
rs78776959	snp	C/T	0.0524604	0.153226	intron-variant	NEB	GRCh38.p7	2:151663066	TCTCTGTCTTCCTTA[C/T]ATTTAGTCTAAAGGC	4703
rs78789544	snp	C/G	0.0452528	0.143452	intron-variant	NEB	GRCh38.p7	2:151708062	GAACTGTCAGGGCTT[C/G]TGGCAAAGCCATCCC	4703
rs78867421	snp	C/T	0.0225045	0.103662	intron-variant	NEB	GRCh38.p7	2:151707074	TATGAATATGACATA[C/T]TTCCACAAATCAATT	4703
rs78892743	snp	A/G	8.2958e-05	0.00643988	synonymous-codon	NEB	GRCh38.p7	2:151697571	GTTCTGCAGAACAGT[A/G]TCGAGCTTGAATTTG	4703
rs78895794	snp	C/G	0.0941369	0.195465	intron-variant	NEB, RIF1	GRCh38.p7	2:151495948	CCTACTCCACCACCC[C/G]ACACGTACCCGTCCT	4703
rs78916288	snp	A/G/T	0.00614057	0.055071	NEB	2	allele_origin=G(germline)/A(germline)	2:151663544	AAATGTGGTTTTCAC[A/G/T]TACATCACTTTGAAT	4703
rs78982474	snp	A/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151486568	TGTCCGTAGCAGCAT[A/T]ACTCATAATAGCCAA	4703
rs79018537	snp	A/G	0.00716266	0.059414	intron-variant	NEB	GRCh38.p7	2:151622305	GTTTGGTAAAGTTTC[A/G]TTTTAATACTTTCAG	4703
rs79019047	snp	A/C	0.5	0	intron-variant	NEB	GRCh38.p7	2:151635707	GCAAAACTCTGTCTC[A/C]AAAAAAAAAAAAAAA	4703
rs79023475	snp	C/T	0.0569829	0.158885	intron-variant	NEB, RIF1	GRCh38.p7	2:151526497	ATATAGTCACACTTA[C/T]GTTCACAGCACGCTC	4703
rs79026325	snp	C/T	0.00914312	0.0669923	intron-variant	NEB	GRCh38.p7	2:151619214	AGGAAGCCTGAATCC[C/T]TAGGAAGATTTATAC	4703
rs79061878	snp	A/C			intron-variant	NEB	GRCh38.p7	2:151680490	TTAAGAGAAGTCCCT[A/C]TTACCTTTTCCTTAG	4703
rs79064738	snp	A/T	0	0	intron-variant	NEB, RIF1	GRCh38.p7	2:151531334	TTTTTTTTTTTTTTT[A/T]GAGACAGAGTCTCAC	4703
rs79092350	snp	C/T			intron-variant	NEB, RIF1	GRCh38.p7	2:151512652	CTGATCTGAAGAATC[C/T]CTTAAGGTATTTATT	4703
rs79129822	snp	C/T	0.0333695	0.124785	intron-variant	NEB	GRCh38.p7	2:151544033	TCTCCATGGTTTTTA[C/T]TAAAAACAGATTCGT	4703
rs79130216	snp	A/G	0.0325976	0.123435	intron-variant	NEB	GRCh38.p7	2:151611434	GGTTGCTGTTGATGG[A/G]TATAGTATAAAAGAG	4703
rs79167650	snp	A/C/T	0.000399281	0.0141238	intron-variant	NEB	GRCh38.p7	2:151637340	TGAATCAAGGCACCA[A/C/T]TGTGGAGGGGAAGCG	4703
rs79205344	snp	A/G	0.000381684	0.0138093	missense	NEB	GRCh38.p7	2:151568646	TCGCCACTTTGTTTC[A/G]CTGTCACATAATCAA	4703
rs79231198	snp	C/T	0.00914312	0.0669923	intron-variant	NEB, RIF1	GRCh38.p7	2:151487431	ATTCAAATTCACAAA[C/T]AGATTTCCTTTCCCC	4703
rs79262260	snp	A/G	0.029116	0.117091	intron-variant	NEB	GRCh38.p7	2:151695038	TGCCAGATAATCTTA[A/G]TACTCATTTATAGAA	4703
rs79285434	snp	A/G	0.00119737	0.0244387	intron-variant	NEB	GRCh38.p7	2:151695997	ACTGTCAGTGCTCAC[A/G]TACCAGAGCCACTTT	4703
rs79315981	snp	C/G	0.0142736	0.0832652	intron-variant	NEB	GRCh38.p7	2:151546933	TTTAAGTCTCTAACC[C/G]TGAGCTGAGGAGAGA	4703
rs79395391	snp	A/C/G	0.0023933	0.0345097	intron-variant	NEB	GRCh38.p7	2:151654431	GGGCTTACTATTTTG[A/C/G]AGATAGATATTAAGA	4703
rs79402065	snp	A/G	0.00137948	0.0262266	intron-variant	NEB	GRCh38.p7	2:151666419	ATTTGAAAACAAAGG[A/G]CAAACAGAAGTTGGC	4703
rs79415884	snp	A/G/T	0.000335216	0.0129423	intron-variant	NEB	GRCh38.p7	2:151639834	TAGGAGCCCCACTTC[A/G/T]ATTCTTAATTTTGAA	4703
rs79421278	snp	A/T	0.00557542	0.0525036	intron-variant	NEB	GRCh38.p7	2:151696554	CCTTTTGAATAAACT[A/T]GATAAGTCATTGGAT	4703
rs79487307	snp	C/T	0.0501905	0.150254	intron-variant	NEB, RIF1	GRCh38.p7	2:151500754	AGGCATGTGCCACCA[C/T]GCTTGGCTAATTTTT	4703
rs79506457	in-del	-/GGT			intron-variant	NEB	GRCh38.p7	2:151723775	TTTTTTTTTTTTTTT[-/GGT]CATTATTTGTCATTG	4703
rs79524813	snp	C/T	0.00889401	0.0660901	synonymous-codon	NEB	GRCh38.p7	2:151727790	CTTCCTCCTCTCCAC[C/T]GGCTTTGCTGATGCT	4703
rs79552023	snp	A/G	0.0916144	0.193427	intron-variant	NEB, RIF1	GRCh38.p7	2:151501088	TAAAAAGAGTTCCAA[A/G]TAAATAAGAGCTTTA	4703

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