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

TOM1L2

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs3677	snp	A/C	0.00806438	0.0629854	intron-variant	TOM1L2	GRCh38.p7	17:17868937	GGGAAAGAGGAAATC[A/C]TTTTTCTTACTAGAG	146691
rs745401	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17901673	GGAACTGAAGACATG[C/T]AATAGAGCAAGATAA	146691
rs950966	snp	C/T	0.387263	0.208947	intron-variant	TOM1L2	GRCh38.p7	17:17880434	GGAGAAAGTGTATGA[C/T]GTCTCTGTTGCTGGA	146691
rs998179	snp	C/T	0.00279162	0.0372561	intron-variant	TOM1L2	GRCh38.p7	17:17884458	AGTGAGACAGCTGGT[C/T]GACTGGTGATTAAGT	146691
rs1052299	snp	C/T	0.453697	0.14494	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847105	GTGACATTTGGCTTA[C/T]CAGCATTTGAGAAGG	146691
rs1108646	snp	C/T	0.495927	0.0449436	intron-variant	TOM1L2	GRCh38.p7	17:17848164	GCATCTCCTCAGTCC[C/T]CCATTGGTGGGCAAG	146691
rs1108648	snp	A/G	0.442655	0.159323	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847244	ATGCCTGAGAAGGTC[A/G]CTGAGCCAGGCAGAG	146691
rs1737972	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17893354	TAGGAAGAACCATGT[A/T]AGAGCTACGTGCGGG	146691
rs1737973	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17893310	CAGGGCAGGGGCCAA[A/C]TCTGGGTCAGGCGGA	146691
rs1759082	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17893299	CCAAATCTGGGTCAG[C/G]CGGAGCAAGGTAAGg	146691
rs1889014	snp	A/G	0.346147	0.230772			GRCh38.p7	17:17863851	caacaaaaGTGTAGT[A/G]TCCAccaggggtggt	146691
rs1889015	snp	C/T	0.0528381	0.153711			GRCh38.p7	17:17844512	GGAAAGGTGACCATC[C/T]GTCTGTCCTCCTGTC	146691
rs2236513	snp	G/T	0.476918	0.104919	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17844052	TCTGCACTGTCGGCT[G/T]TGGGGACGTCTCACC	146691
rs2274893	snp	A/G	0.0329836	0.124112	intron-variant	TOM1L2	GRCh38.p7	17:17885030	AGGTGTTATTTCTCT[A/G]TCTCTTCTCCAAGGA	146691
rs2350977	snp	C/T	0.455263	0.142713	intron-variant	TOM1L2	GRCh38.p7	17:17899465	AAAGTTGGAGTGGAG[C/T]TGTTTGGAAGTTGGA	146691
rs3075551	snp	A/G	0.46875	0.121031	intron-variant	TOM1L2	GRCh38.p7	17:17894975	CATACATACATACAT[A/G]CATGCATGCATGCAT	146691
rs3075553	in-del	-/GCATGCAT	0	0	intron-variant	TOM1L2	GRCh38.p7	17:17894994	catgcatgcatgcat[-/GCATGCAT]aaaataatgcacata	146691
rs3183702	snp	C/T	0.477004	0.104734	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17843975	ACCCCAGAGACATTG[C/T]CTGTCAGCCCCTGAA	146691
rs3737121	snp	C/T	0	0	intron-variant	TOM1L2	GRCh38.p7	17:17849136	AGAACCAGCCTGCAC[C/T]GTTTTTGGAGTTTTC	146691
rs3737122	snp	A/G	0.105214	0.203807	intron-variant	TOM1L2	GRCh38.p7	17:17849078	CTAAAACATGTTTGA[A/G]TTTTTTGCTTTTGTT	146691
rs3737123	snp	A/G	0.136847	0.222927	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17846794	TGTGGAGGGACTTGC[A/G]CTGGAGGTATTGCTC	146691
rs3744113	snp	C/T	0.44858	0.151875	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17845331	AGGCCTCTCCAATGA[C/T]GCCTGGCAACCAGCT	146691
rs3744114	snp	C/T	0.0379877	0.132479	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17846472	TACATGTTACCAGCC[C/T]CTAGCTGCTCTGCCT	146691
rs3744115	snp	A/G	0.453575	0.145111	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17846508	CAGGATCAGCTTGGG[A/G]AGAGAGTATAAATTG	146691
rs4077198	snp	A/G	0.455502	0.142369	intron-variant	TOM1L2	GRCh38.p7	17:17931249	TGGAGAATTGGGGAA[A/G]TCTGTAGAAGAGGAA	146691
rs4077828	snp	A/T	0.455502	0.142369	intron-variant	TOM1L2	GRCh38.p7	17:17930330	TGGTCTTAGGAAATG[A/T]CCAAATCAGAGACTC	146691
rs4244602	snp	A/G	0.392325	0.205532	intron-variant	TOM1L2	GRCh38.p7	17:17938142	AGAGGACCCAGGACT[A/G]CAGGTAGAAATGAGA	146691
rs4257260	snp	A/G	0.455024	0.143057	intron-variant	TOM1L2	GRCh38.p7	17:17953689	CACACATGAAGACAC[A/G]TGAGTGGGGGGAGCA	146691
rs4341796	snp	A/C	0.377385	0.215112	intron-variant	TOM1L2	GRCh38.p7	17:17935710	CATCTCTAAAGTCCA[A/C]CAATGATGCCATCAT	146691
rs4343339	snp	C/T	0.455024	0.143057	intron-variant	TOM1L2	GRCh38.p7	17:17969275	TTGGTCAGGCTGGCC[C/T]CCAACTCCTGACCTC	146691
rs4413022	snp	C/G	0.448066	0.152544	intron-variant	TOM1L2	GRCh38.p7	17:17954966	CCCTTCCTGACCTCC[C/G]TTTCTTTTGCTGTTG	146691
rs4414547	snp	G/T	0.455024	0.143057	intron-variant	TOM1L2	GRCh38.p7	17:17955738	actgacttcaagaat[G/T]aagccatagaccctc	146691
rs4458058	snp	A/G	0.021333	0.101051	intron-variant	TOM1L2	GRCh38.p7	17:17910008	cattccagcctaggc[A/G]acagagtaagaccct	146691
rs4470201	snp	A/G	0.455858	0.141853	intron-variant	TOM1L2	GRCh38.p7	17:17941556	GGGATTCCAAGCCAC[A/G]AGGAGATATCCACGG	146691
rs4471742	snp	C/T	0.485392	0.0842056	upstream-variant-2KB, intron-variant	TOM1L2, DRC3	GRCh38.p7	17:17974457	GCTCACCGCAACCTC[C/T]GCCTCCCGGTTTCAA	146691
rs4534911	snp	A/G	0.394538	0.203982	intron-variant	TOM1L2	GRCh38.p7	17:17949016	GAAGGGGCCACATAC[A/G]GAGTGACTGTCCCAT	146691
rs4553680	snp	A/G	0.386313	0.209568	intron-variant	TOM1L2	GRCh38.p7	17:17954408	ACCTCAGCCTCCCAG[A/G]TTCAAATGATTCTCC	146691
rs4616339	snp	C/G	0	0	intron-variant	TOM1L2	GRCh38.p7	17:17952549	ggtgcgtgctgccac[C/G]cctggctaagttttt	146691
rs4616340	snp	C/T	0.448452	0.152042	intron-variant	TOM1L2	GRCh38.p7	17:17958046	AGTAAGTCGAGATTG[C/T]GCCACTGCACTCCAG	146691
rs4621034	snp	C/T	0.42	0.183303	intron-variant	TOM1L2	GRCh38.p7	17:17952381	TCTTTATTTTCTTTt[C/T]ttttttttttttttt	146691
rs4624238	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17954331	TTTTTTTTTTTTTTG[G/T]GATGGAGCTTCGCTT	146691
rs4924822	snp	A/G	0.476401	0.106032	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17844699	AAGGCCCATGGTGCC[A/G]GGGGCCCAACTGCAC	146691
rs4924823	snp	A/G	0.484209	0.0874434	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17861188	TAGGATTGGAACCCC[A/G]GCTTGCTGTCTGCTC	146691
rs4924824	snp	C/T	0.0209421	0.100162	intron-variant	TOM1L2	GRCh38.p7	17:17867077	ATATCAACTCTGCCA[C/T]GGCTTCCTCTGTGTG	146691
rs4924825	snp	A/G	0.0209421	0.100162	intron-variant	TOM1L2	GRCh38.p7	17:17884128	AGGGCTTTGATCCCA[A/G]GGCTGATGGAATCAA	146691
rs4924826	snp	A/C	0.167809	0.236103	intron-variant	TOM1L2	GRCh38.p7	17:17894732	GGTCAGGAATTCAAG[A/C]CCAGCCTAGCCAACA	146691
rs4924827	snp	C/G	0.00755907	0.0610114	intron-variant	TOM1L2	GRCh38.p7	17:17930247	GCTCCAGAAAGTGGG[C/G]TATAGAGAATTACCA	146691
rs4925120	snp	C/T	0.464416	0.128553	intron-variant	TOM1L2	GRCh38.p7	17:17851319	AGGAAGGCGCTGCCA[C/T]GCAGGCTGATTTTGA	146691
rs4925123	snp	C/T	0.387263	0.208947	intron-variant	TOM1L2	GRCh38.p7	17:17881060	AGACCTTTAGCTTCT[C/T]AGGGCAGGAACTCAG	146691
rs4925124	snp	A/T	0.147991	0.228242	intron-variant	TOM1L2	GRCh38.p7	17:17887580	CTCCGGGCTCAAGCA[A/T]TCCTCCCACTTTAGC	146691
rs4925125	snp	C/T	0.480853	0.0959518	intron-variant	TOM1L2	GRCh38.p7	17:17891130	CCAGGCAGAAGCTTG[C/T]GAGGCATCTCAAGGC	146691
rs4925126	snp	A/G	0.479904	0.0982045	intron-variant	TOM1L2	GRCh38.p7	17:17895319	TTTCTGACTACCTCA[A/G]TTATTCTCATTTGCC	146691
rs4925127	snp	C/G	0.0209421	0.100162	intron-variant	TOM1L2	GRCh38.p7	17:17903141	TGCCACTGCACTAGT[C/G]TCCGTAGCTATATAT	146691
rs4925128	snp	A/G	0.144632	0.226711	intron-variant	TOM1L2	GRCh38.p7	17:17903636	AAAAAAAAAATGTTG[A/G]GTAAAACAGATGGAA	146691
rs4925129	snp	A/G	0.395635	0.2032	intron-variant	TOM1L2	GRCh38.p7	17:17903872	GGATCTACTTAGTGA[A/G]AGAGGTGACGAGAAC	146691
rs4925130	snp	A/G	0.390651	0.206682	intron-variant	TOM1L2	GRCh38.p7	17:17904544	ATGAGGGGCCTGGTT[A/G]GGGTTTTTAACCTAA	146691
rs4925131	snp	A/G	0.0209421	0.100162	intron-variant	TOM1L2	GRCh38.p7	17:17904684	AGTGCAGACACCAGA[A/G]AATGCAGCACCTGAC	146691
rs4925132	snp	C/G	0.0248432	0.108648	intron-variant	TOM1L2	GRCh38.p7	17:17904757	CCAATGTCACCCTGT[C/G]TATCCTAGACAGCTT	146691
rs4997327	snp	A/G	0.0448719	0.142907	intron-variant	TOM1L2	GRCh38.p7	17:17920872	AACTCCTGACCTCAG[A/G]TGATCCACCCGCCTC	146691
rs5002487	snp	A/G	0.387263	0.208947	intron-variant	TOM1L2	GRCh38.p7	17:17929146	TATAGTAAAGGGTAC[A/G]AGCCAGAATGCAGTC	146691
rs5819629	in-del	-/A	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17855963	ATATTTGTTGTAAAG[-/A]AAAAAAAAAAAACAA	146691
rs5819630	in-del	-/G			intron-variant	TOM1L2	GRCh38.p7	17:17880245	CTCTGAGAGGCTGGG[-/G]CAGTGTCAATAGCAC	146691
rs5819637	in-del	-/T/TT			intron-variant	TOM1L2	GRCh38.p7	17:17938781	TTTTTTTTTTTTTTT[-/T/TT]AATATTTTGTAAAGA	146691
rs5819638	in-del	-/T/TT	0.489142	0.0728777	intron-variant	TOM1L2	GRCh38.p7	17:17954312	TTTTTTTTTTTTTTT[-/T/TT]GTGATGGAGCTTCGC	146691
rs6502618	snp	A/G	0.46137	0.133501	downstream-variant-500B	TOM1L2	GRCh38.p7	17:17843427	AGGGTCCCCATGGCC[A/G]CCCCTGCTTAAATAA	146691
rs6502619	snp	C/G	0.377582	0.214995	intron-variant	TOM1L2	GRCh38.p7	17:17876390	CCTGTGGTGGGCTGC[C/G]AAATGCTGCCAAATG	146691
rs6502622	snp	A/G	0.448963	0.151372	intron-variant	TOM1L2	GRCh38.p7	17:17931377	GATCTTTGGAGTCAG[A/G]CCAATTGAGCTCAAA	146691
rs6502624	snp	A/G	0.455977	0.141681	intron-variant	TOM1L2	GRCh38.p7	17:17944622	TCCCCAAAGCACCAG[A/G]CACCTGCTTCTCTTG	146691
rs6502625	snp	C/G	0.346811	0.230494	intron-variant	TOM1L2	GRCh38.p7	17:17944972	CGTACTCCTGACATT[C/G]CAGCAGATGCTGCCC	146691
rs6502626	snp	C/T	0.474363	0.110278	intron-variant	TOM1L2	GRCh38.p7	17:17946136	gcctgcctcagcctc[C/T]gaaagtgctgggatt	146691
rs6502627	snp	C/T	0.455383	0.142541	intron-variant	TOM1L2	GRCh38.p7	17:17946357	tcctgtacctgttag[C/T]agtcacttcccattc	146691
rs6502629	snp	A/G	0.347914	0.230028	intron-variant	TOM1L2	GRCh38.p7	17:17966328	ACAGGGCCACTGAAT[A/G]AATAAATGAACAAAT	146691
rs7207043	snp	A/G	0.448836	0.15154	intron-variant	TOM1L2	GRCh38.p7	17:17915874	ggttgttaagctgta[A/G]gagttctttatatat	146691
rs7207395	snp	C/T	0.377385	0.215112	intron-variant	TOM1L2	GRCh38.p7	17:17916021	cctgtggttttggta[C/T]catatctcagaaatc	146691
rs7207535	snp	C/T	0.00517822	0.0506191	intron-variant	TOM1L2	GRCh38.p7	17:17964690	ttgagcccagtaggt[C/T]gaggctttaactacg	146691
rs7208190	snp	A/G	0.455502	0.142369	intron-variant	TOM1L2	GRCh38.p7	17:17916343	ctcccaaagtgctgg[A/G]attacaggcatgaat	146691
rs7208950	snp	C/T	0	0	intron-variant	TOM1L2	GRCh38.p7	17:17948241	GGATAATCTTGATAC[C/T]AAGATAAATACGCCC	146691
rs7209478	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17895399	GGTCCAAGCAAGTGG[A/G]CTTTACCTGGACAAA	146691
rs7209628	snp	A/G	0	0	intron-variant	TOM1L2	GRCh38.p7	17:17895473	TGCGACTATATGCCA[A/G]GCACTATGAGAGATC	146691
rs7213225	snp	C/T	0.455024	0.143057	intron-variant	TOM1L2	GRCh38.p7	17:17965797	TCAGTCTCTGGCACA[C/T]AGGAATACAACATTA	146691
rs7213566	snp	C/T	0	0	intron-variant	TOM1L2	GRCh38.p7	17:17852373	ACTCTGAGCAGGTAT[C/T]TACGATGCCACCAGA	146691
rs7214002	snp	C/G	0.479904	0.0982045	intron-variant	TOM1L2	GRCh38.p7	17:17948790	CCAGAGCAAGGCAGG[C/G]GTCCTAGGAAGGGCT	146691
rs7214028	snp	C/T	0.148996	0.228688	intron-variant	TOM1L2	GRCh38.p7	17:17886872	CCCAAGTTGGGCCAA[C/T]CAGATGCTCCTCCTT	146691
rs7214536	snp	A/G	0.453575	0.145111	intron-variant	TOM1L2	GRCh38.p7	17:17949132	GGTTTCATGCCATGC[A/G]TTTCTCACACAGGAG	146691
rs7214844	snp	A/C	0.0345262	0.126772	intron-variant	TOM1L2	GRCh38.p7	17:17927862	tacagccagggtttc[A/C]ctatgttacccaggc	146691
rs7217349	snp	C/T	0.0209421	0.100162	intron-variant	TOM1L2	GRCh38.p7	17:17901690	ATGTCTTCAGTTCCT[C/T]CTCTGTGCCCTCTCC	146691
rs7218054	snp	A/G	0.0402882	0.136092	intron-variant	TOM1L2	GRCh38.p7	17:17872132	TCACAATTACTGTAC[A/G]CAGGAAAACCAACAA	146691
rs7218594	snp	A/C	0.0704125	0.17392	intron-variant	TOM1L2	GRCh38.p7	17:17910873	tgtgcccagccCCAA[A/C]ACTCTTGATGGTTGG	146691
rs7221575	snp	A/T	0.453209	0.145623	intron-variant	TOM1L2	GRCh38.p7	17:17945290	CACACACACACACAC[A/T]CTCTCTCTCTCTCTC	146691
rs7221934	snp	C/G	0.0770498	0.180522	intron-variant	TOM1L2	GRCh38.p7	17:17863558	GTGGGTGGGAAGACA[C/G]TAGACtttttttttt	146691
rs7222480	snp	G/T	0.387263	0.208947	intron-variant	TOM1L2	GRCh38.p7	17:17915503	ctattcaattttttt[G/T]gcccctcaccccttt	146691
rs7224621	snp	C/T	0.0387552	0.1337	intron-variant	TOM1L2	GRCh38.p7	17:17942296	TCCATTAATAAATAG[C/T]AGTAATAAGGATGGG	146691
rs7224815	snp	A/T	0.337386	0.23423	intron-variant	TOM1L2	GRCh38.p7	17:17942486	CCAGAAAATCATATC[A/T]ATTTAAAGGACATTT	146691
rs7501812	snp	A/G	0.499954	0.00478616	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847593	GTGTCCACGGGGTGC[A/G]AGCGGGGACCCGCCA	146691
rs7503334	snp	C/T	0.377582	0.214995	intron-variant	TOM1L2	GRCh38.p7	17:17876144	ACTGGATGACATAAT[C/T]GCAATCTTTAAAGAT	146691
rs8065076	snp	A/G	0	0	intron-variant	TOM1L2	GRCh38.p7	17:17878783	GTGTGGGGCCTTGCA[A/G]TTCACAGCATCCTTC	146691
rs8065416	snp	C/T	0.454664	0.143571	intron-variant	TOM1L2	GRCh38.p7	17:17947848	ATTCATTTTTAATTT[C/T]TTTTGGTAGCATGAG	146691
rs8065497	snp	A/G	0.337158	0.234315	intron-variant	TOM1L2	GRCh38.p7	17:17879335	GCTTGGGTCAAAGAA[A/G]GTTATTTTCTTTTCT	146691
rs8065563	snp	A/G	0.37778	0.214877	intron-variant	TOM1L2	GRCh38.p7	17:17879090	GAATCCTCAGTGTTA[A/G]GGAAAAGCATGGGAG	146691
rs8065970	snp	A/G	0.455024	0.143057	intron-variant	TOM1L2	GRCh38.p7	17:17955457	gattctccagcctcc[A/G]tctcccacgtagctg	146691
rs8066145	snp	A/G	0.455144	0.142885	intron-variant	TOM1L2	GRCh38.p7	17:17903600	CCTGGGCGACAGAGC[A/G]AGACTCCATCTCAAA	146691
rs8066353	snp	A/T	0.089084	0.191327	intron-variant, downstream-variant-500B	TOM1L2, LOC100507131	GRCh38.p7	17:17858196	GAACCAGCTTTTACA[A/T]AAGCAATTCTACTTT	146691
rs8066528	snp	A/G	0.0704125	0.17392	intron-variant	TOM1L2	GRCh38.p7	17:17925495	ACTAAGAAAGAAAGT[A/G]GCAAACTAATGACCA	146691
rs8066865	snp	A/G	0.0387552	0.1337	intron-variant	TOM1L2	GRCh38.p7	17:17934367	gaggggtatcacttg[A/G]gcccggggatcaagg	146691
rs8066982	snp	C/T	0.455024	0.143057	intron-variant	TOM1L2	GRCh38.p7	17:17948063	CAATTCTAAGAGATA[C/T]ATATTAGTCATAATT	146691
rs8067044	snp	A/C/T	0.315516	0.241263	intron-variant	TOM1L2	GRCh38.p7	17:17903631	AAAAAAAAAAAAAAA[A/C/T]GTTGGGTAAAACAGA	146691
rs8068175	snp	C/T	0.445592	0.155704	intron-variant, upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17971172	TTCAGCTTTGGTAAA[C/T]TTAATATGAGGTGGG	146691
rs8068281	snp	G/T	0.378765	0.214288	intron-variant	TOM1L2	GRCh38.p7	17:17912844	gcaggcggctgggag[G/T]tggaggttgtagcga	146691
rs8068820	snp	A/G	0.455502	0.142369	intron-variant	TOM1L2	GRCh38.p7	17:17930805	TTATTGCAACTAGAC[A/G]CTAATTAGGCCCATG	146691
rs8069907	snp	A/G	0.0178098	0.0926698	intron-variant	TOM1L2	GRCh38.p7	17:17939898	AATGGAAGTGTTAAG[A/G]ATTCTGCTTTGggcc	146691
rs8070128	snp	C/T	0.395635	0.2032	intron-variant	TOM1L2	GRCh38.p7	17:17901411	GTCAGGCTCCTCAGG[C/T]AGTGCTCACAGCCTC	146691
rs8070462	snp	C/T	0.089084	0.191327	intron-variant	TOM1L2	GRCh38.p7	17:17946685	GCAGGAGGCCTGTTT[C/T]GCTCTCTAAACATCA	146691
rs8070624	snp	A/G	0.336474	0.234568	intron-variant	TOM1L2	GRCh38.p7	17:17940082	cctgtaatcccagct[A/G]cctgagaggctgaag	146691
rs8070722	snp	C/T	0.455263	0.142713	intron-variant	TOM1L2	GRCh38.p7	17:17910248	ccaggagctcaggat[C/T]gtcagtggcagagcc	146691
rs8070748	snp	A/G	0.455024	0.143057	intron-variant	TOM1L2	GRCh38.p7	17:17956107	agcctcccccgcacg[A/G]aaaaggacccaagtg	146691
rs8073001	snp	G/T	0.455144	0.142885	intron-variant	TOM1L2	GRCh38.p7	17:17928402	CGCTAAGTGGAAATC[G/T]GCATAGGAATGCTAA	146691
rs8075594	snp	A/G	0.126909	0.217598	intron-variant	TOM1L2	GRCh38.p7	17:17968601	ACTTGTGGGGCGGAG[A/G]TTGCAGTGAGCTTAG	146691
rs8075965	snp	A/T	0.448066	0.152544	intron-variant	TOM1L2	GRCh38.p7	17:17949866	TTATTtttatttttt[A/T]aattttatttattta	146691
rs8076747	snp	C/T	0.47852	0.101384	intron-variant	TOM1L2	GRCh38.p7	17:17950281	TGTGCCTCAGTCTTC[C/T]GAGTAGCTGGGATTA	146691
rs8077338	snp	C/T	0.336245	0.234652	intron-variant	TOM1L2	GRCh38.p7	17:17957232	gcaatcctcctgcct[C/T]ggcctcccaaagtgc	146691
rs8077530	snp	C/T	0.448066	0.152544	intron-variant	TOM1L2	GRCh38.p7	17:17950140	TGCTGGGATTACAGG[C/T]GTGAGTCACCACACC	146691
rs8078001	snp	G/T	0.0178098	0.0926698	intron-variant	TOM1L2	GRCh38.p7	17:17929317	CAGCAGGCTTTGGGT[G/T]GGTGAGAGGGGTTGA	146691
rs8078105	snp	C/T	0.455024	0.143057	intron-variant	TOM1L2	GRCh38.p7	17:17950468	ctagcctctcttttt[C/T]ttttttttagagaca	146691
rs8078138	snp	C/T	0.387074	0.209071	intron-variant	TOM1L2	GRCh38.p7	17:17907937	tagtgaaaacaacag[C/T]acttacctgatatat	146691
rs8078252	snp	A/G	0.126564	0.217402	intron-variant	TOM1L2	GRCh38.p7	17:17899355	CTTAAAACCCAACAA[A/G]TTTTGTGTTTTTAGG	146691
rs8078368	snp	A/G	0.0704125	0.17392	intron-variant	TOM1L2	GRCh38.p7	17:17937975	GCCACTCACAGAAAG[A/G]TCTCCACTGATGTCC	146691
rs8078583	snp	C/T	0.396	0.202938	intron-variant	TOM1L2	GRCh38.p7	17:17908151	GTGTTGGGTGTTTCA[C/T]GTACATTATTTTATC	146691
rs8078811	snp	C/T	0.0704125	0.17392	intron-variant	TOM1L2	GRCh38.p7	17:17899164	CACATGCAAGTATTA[C/T]TTATTCAAAACCCTA	146691
rs8079321	snp	C/T	0.484138	0.0876334	intron-variant	TOM1L2	GRCh38.p7	17:17857475	AAAAGTGAATACTGC[C/T]CGGAGCTCCGGAGAC	146691
rs8080061	snp	C/T	0.462691	0.131387	intron-variant	TOM1L2	GRCh38.p7	17:17873075	CAGGCACTTGCCACA[C/T]TGCTTAAGGGCTCCT	146691
rs8080823	snp	C/T	0.386313	0.209568	intron-variant	TOM1L2	GRCh38.p7	17:17960734	TCCAAAAAAACAAAA[C/T]AGAGTGATAATACCT	146691
rs8080949	snp	C/T	0.0894459	0.191631	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17845261	TGTCAGCATGGCCAA[C/T]GGCCTCCTGCCAGCC	146691
rs8081654	snp	C/T	0	0	intron-variant	TOM1L2	GRCh38.p7	17:17903469	ACAAAAAAAATTAGC[C/T]GGGCGTGGTGGCGGG	146691
rs9635697	snp	A/T	0.455024	0.143057	intron-variant	TOM1L2	GRCh38.p7	17:17967080	CATCTACCCTATTAG[A/T]TGTGTCCCTCTAGAG	146691
rs9635698	snp	C/T	0.455024	0.143057	intron-variant	TOM1L2	GRCh38.p7	17:17968570	CTTGGGAGGCTGAGA[C/T]AGGAGAATCGCTTGA	146691
rs9674691	snp	C/T	0.444444	0.157135	intron-variant	TOM1L2	GRCh38.p7	17:17912021	gaatttttcttagta[C/T]agaacaaaatgaaaa	146691
rs9890341	snp	C/G	0.455263	0.142713	intron-variant	TOM1L2	GRCh38.p7	17:17919861	ACCCTACCATCCCAC[C/G]CCCCAGCCGCCAGGA	146691
rs9892833	snp	C/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17937958	AACCACACTCCATTC[C/G]TGCCACTCACAGAAA	146691
rs9892963	snp	A/T	0.464629	0.128197	intron-variant	TOM1L2	GRCh38.p7	17:17945288	CACACACACACACAC[A/T]CACTCTCTCTCTCTC	146691
rs9893690	snp	A/T	0.485118	0.0849685	intron-variant	TOM1L2	GRCh38.p7	17:17850532	AAAACATGCTCCCCC[A/T]ACACTCCCTCCCCCA	146691
rs9895335	snp	A/G	0.462909	0.131034	intron-variant	TOM1L2	GRCh38.p7	17:17864453	ctgaccttgtgatcc[A/G]cccgcctcggcctcc	146691
rs9895750	snp	C/T	0.396364	0.202676	intron-variant	TOM1L2	GRCh38.p7	17:17864505	gttagccaccgcacc[C/T]ggctttttttttttt	146691
rs9895909	snp	A/T	0	0	intron-variant	TOM1L2	GRCh38.p7	17:17917607	cctggcttcattgca[A/T]ttttaactgggattt	146691
rs9897374	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17864492	tgggattacaggcgt[G/T]agccaccgcacccgg	146691
rs9897573	snp	A/G	0.0150606	0.0854603	intron-variant	TOM1L2	GRCh38.p7	17:17896420	AGAGCAACAGTGGCA[A/G]GAACCACTGCCCGCC	146691
rs9900947	snp	A/T	0.0193772	0.0965046	intron-variant	TOM1L2	GRCh38.p7	17:17909077	ttccagctactcagg[A/T]ggctgaggcaggaga	146691
rs9904163	snp	C/T	0.455383	0.142541	intron-variant	TOM1L2	GRCh38.p7	17:17927239	CCAAAGGGACAGGCC[C/T]GACATTATTTTCAGC	146691
rs9905284	snp	A/G	0.455263	0.142713	intron-variant	TOM1L2	GRCh38.p7	17:17962438	ctgcttcagcctccc[A/G]agtacctgggactac	146691
rs9907246	snp	C/T	0.405603	0.195673	intron-variant	TOM1L2	GRCh38.p7	17:17867651	AAACTCCAAATGCCA[C/T]GGGCAGCGGTAGCTA	146691
rs9907287	snp	C/T	0.484138	0.0876334	intron-variant	TOM1L2	GRCh38.p7	17:17870804	GATGCCCTCAAGCCC[C/T]GCACTGAGCCACACA	146691
rs9908017	snp	C/T	0.462909	0.131034	intron-variant	TOM1L2	GRCh38.p7	17:17871108	AGGTGTGGTGGCTCA[C/T]GCCTGTAATCCCAAA	146691
rs9908299	snp	C/T	0.404733	0.196361	intron-variant	TOM1L2	GRCh38.p7	17:17871254	CGGGCACCTGTAGTC[C/T]CAGCTACTTGGGAGA	146691
rs9908832	snp	C/T	0.479744	0.0985793	intron-variant	TOM1L2	GRCh38.p7	17:17967754	CTGGGATTATACGCG[C/T]GTGCCACCATGCCCA	146691
rs9908994	snp	C/T	0.0150606	0.0854603	intron-variant	TOM1L2	GRCh38.p7	17:17901642	TTCTGTCACCCTGAA[C/T]ATGCCCTCCCCATTA	146691
rs9910488	snp	C/T	0.0154538	0.0865337	intron-variant	TOM1L2	GRCh38.p7	17:17904735	GATTCCAGACCCTCC[C/T]GCTCCCCCAATGTCA	146691
rs9911281	snp	C/G	0.484066	0.0878235	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17859143	GTGCAATGGCATGAT[C/G]TCGGCTCACTGCAAC	146691
rs9911890	snp	A/G	0.232651	0.249397	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17859656	GAGGCCAAGACGGGC[A/G]GAGTGCCTGAGGTCA	146691
rs9912895	snp	A/G	0.448836	0.15154	intron-variant	TOM1L2	GRCh38.p7	17:17922706	AAATAAGTTAGTGAT[A/G]TAAGACACGAAACAG	146691
rs9913724	snp	A/G	0.448836	0.15154	intron-variant	TOM1L2	GRCh38.p7	17:17915787	ttggccccccaaagt[A/G]ctaggatcacaggca	146691
rs9914083	snp	A/G	0	0	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17843782	CACAATTAAGTGCAA[A/G]CTTTAGGAAATAAAT	146691
rs9914127	snp	A/T	0.485049	0.0851591	upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17972522	CGTTACACCTCTGTC[A/T]GCAAAGCCCCCACCC	146691
rs9915030	snp	A/G	0	0	intron-variant	TOM1L2	GRCh38.p7	17:17916094	tttttttttttttga[A/G]atggagtcttgcgct	146691
rs9915248	snp	C/T	0.454544	0.143743	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17844200	TGGCCTACCCCAAGC[C/T]ATCCAGAAGGCTGGG	146691
rs9915374	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17852699	ggagaaacccagtct[C/T]tactaaaaatacaaa	146691
rs9915776	snp	A/G	0.476227	0.106402	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17845742	CAAGTGAAGCCAGCT[A/G]ACTTCAGCAGTCTTC	146691
rs10048206	snp	A/G	0.455024	0.143057	intron-variant	TOM1L2	GRCh38.p7	17:17963583	AAATTTTTAAATGAG[A/G]TAAGTATGCACAGCA	146691
rs10538817	in-del	-/CA	0.455383	0.142541	intron-variant	TOM1L2	GRCh38.p7	17:17946278	ATTAGTACATATATT[-/CA]CAGAGTTGTGCAACC	146691
rs10551928	in-del	-/AGG	0.0236746	0.106192	intron-variant	TOM1L2	GRCh38.p7	17:17926653	GGATTGCTTGAGCTC[-/AGG]AGTTCAAGACCAGCC	146691
rs10553875	in-del	-/TCTC			intron-variant	TOM1L2	GRCh38.p7	17:17949835	TAACACTGAATCTGT[-/TCTC]TCTCTCTATTTTTTA	146691
rs10555800	in-del	-/TC	0.441806	0.160345	intron-variant	TOM1L2	GRCh38.p7	17:17969860	GTGAATAGGAATCTT[-/TC]TCTCTCTCTCTCTCT	146691
rs10584478	in-del	-/CTCT			intron-variant	TOM1L2	GRCh38.p7	17:17949842	GAATCTGTTCTCTCT[-/CTCT]ATTTTTTATTTTTAT	146691
rs10664045	in-del	-/T/TT	0	0	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17858236	CTACATTTTTTTTTT[-/T/TT]CTCTTTTCTAGTGGC	146691
rs11078400	snp	A/G	0.483995	0.0880135	intron-variant	TOM1L2	GRCh38.p7	17:17854414	TTAGGAGGCCTCGGT[A/G]TCCTCATCTGTCAGA	146691
rs11078401	snp	A/G	0.0189856	0.0955633	intron-variant	TOM1L2	GRCh38.p7	17:17866138	AAGGTATGAATTGAA[A/G]GTAAGGTGGTACAAC	146691
rs11078403	snp	A/G	0.479663	0.0987666	intron-variant	TOM1L2	GRCh38.p7	17:17900102	CCTGTAATCCTAGCT[A/G]CTCGGGAGGCTGAGG	146691
rs11078404	snp	A/T	0.448963	0.151372	intron-variant	TOM1L2	GRCh38.p7	17:17917173	taaaaaaattaaaaa[A/T]tttaaaaaattagct	146691
rs11078405	snp	G/T	0.395818	0.203069	intron-variant	TOM1L2	GRCh38.p7	17:17921664	GTCAGACAGGTGGGG[G/T]TGGCTGGGAGGATCA	146691
rs11078406	snp	G/T	0.480223	0.0974544	intron-variant	TOM1L2	GRCh38.p7	17:17937509	ACATATGAACCAGAT[G/T]AAACAAAGGTTCTTT	146691
rs11078407	snp	C/T	0.472335	0.114312	intron-variant	TOM1L2	GRCh38.p7	17:17937769	GGTGAACACCACTCA[C/T]GCAAGAGCATAACAA	146691
rs11078408	snp	A/G	0.485049	0.0851591	upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17972697	ACTATTATTGGACAA[A/G]AGACGAGTCAATCAC	146691
rs11078409	snp	C/G	0.485324	0.0843964	upstream-variant-2KB, intron-variant, utr-variant-5-prime	TOM1L2, DRC3	GRCh38.p7	17:17972982	TTGAGAAGGTGAGAC[C/G]TGGGAGCTGAGGCTC	146691
rs11298542	in-del	-/A	0.450105	0.149859	intron-variant	TOM1L2	GRCh38.p7	17:17968665	GTGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA	146691
rs11308511	in-del	-/T	0.0256215	0.110247	intron-variant	TOM1L2	GRCh38.p7	17:17881962	ATAAACATTGGAGAG[-/T]TTTTTTTTCCCCCAA	146691
rs11334951	in-del	-/T	0.4661	0.125701	intron-variant	TOM1L2	GRCh38.p7	17:17863564	TTTTTTTTTTTTTTT[-/T]AAAGAGACAGAGTCT	146691
rs11340467	in-del	-/T	0.455383	0.142541	intron-variant	TOM1L2	GRCh38.p7	17:17926261	TCTGAACATACAGAC[-/T]TAAGGATAAAAGCCT	146691
rs11386510	in-del	-/C	0.145305	0.227022	intron-variant	TOM1L2	GRCh38.p7	17:17904812	TGATGCCACCCTTGG[-/C]CTACGGGACACATTT	146691
rs11418958	in-del	-/T/TT/TTT/TTTTTTCTT/TTTTTTCTTT	0.484209	0.0874434	intron-variant, downstream-variant-500B	TOM1L2, LOC100507131	GRCh38.p7	17:17858226	TTTCTTTTTCCTACA[lengthTooLong]ATTTTTTTTTTCTCT	146691
rs11450891	in-del	-/A	0.480931	0.0957637	intron-variant	TOM1L2	GRCh38.p7	17:17879407	CATTTTATAATCAGG[-/A]AAAAAAATGTTATTA	146691
rs11650649	snp	A/C	0.386884	0.209196	intron-variant	TOM1L2	GRCh38.p7	17:17887005	GACAGCCTATGTTCT[A/C]CAGAAGGAGCAGCTA	146691
rs11650651	snp	A/T	0.105569	0.204058	intron-variant	TOM1L2	GRCh38.p7	17:17945292	CACACACACACACAC[A/T]CTCTCTCTCTCTCTC	146691
rs11650890	snp	C/T	0.377582	0.214995	intron-variant	TOM1L2	GRCh38.p7	17:17887568	TGCAACCTCTGCCTC[C/T]GGGCTCAAGCAATCC	146691
rs11651831	snp	A/G	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17894971	CATACATACATACAT[A/G]CATACATGCATGCAT	146691
rs11652883	snp	A/C	0.00985198	0.0694905	downstream-variant-500B	TOM1L2	GRCh38.p7	17:17843335	CACCGATGTCACAAC[A/C]TGGGCCACGCACAGG	146691
rs11653828	snp	C/T	0.00597247	0.0543191	intron-variant, upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17972114	CCGACGACCAGGATG[C/T]CCAGCCCGCTCGTGG	146691
rs11655294	snp	C/T	0.0170251	0.090679	intron-variant	TOM1L2	GRCh38.p7	17:17938545	TAGAGAATGGAGTGA[C/T]GACGTGCTCTGGAAA	146691
rs11655631	snp	A/G	0.0134861	0.0810011	intron-variant	TOM1L2	GRCh38.p7	17:17926181	gtctcttggagaaaa[A/G]aaaaaaaaaaaGCTA	146691
rs11656840	snp	C/T	0.455502	0.142369	intron-variant	TOM1L2	GRCh38.p7	17:17934040	TTAGGAAAAAAAAAT[C/T]TGAGTAGGCAAGTGT	146691
rs11657074	snp	A/G	0.404733	0.196361	intron-variant	TOM1L2	GRCh38.p7	17:17867041	AGCCAGTCCCACCTG[A/G]GGGCTAGGGAGTGAA	146691
rs11657773	snp	C/T	0.395635	0.2032	intron-variant	TOM1L2	GRCh38.p7	17:17940044	ctaaaaatacaaaaa[C/T]tagccaggtgtggtg	146691
rs11657845	snp	C/G	0.455621	0.142197	intron-variant	TOM1L2	GRCh38.p7	17:17940064	caggtgtggtggcgg[C/G]tgcctgtaatcccag	146691
rs11658309	snp	G/T	0.463018	0.130857	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17858933	atcttggccaggctg[G/T]tcttgaactcccacc	146691
rs11658804	snp	A/G	0.0337553	0.125452	intron-variant	TOM1L2	GRCh38.p7	17:17923356	cagtgagccgagatc[A/G]cgccactgcattcca	146691
rs11869536	snp	A/T	0.455383	0.142541	intron-variant	TOM1L2	GRCh38.p7	17:17923214	ACCAGCCTGGCCAAC[A/T]TGATGAAATCCTGGT	146691
rs11870660	snp	C/T	0.445724	0.155538	upstream-variant-2KB, intron-variant	TOM1L2, DRC3	GRCh38.p7	17:17973782	CCCAACCAATTTTCT[C/T]CTTATTAATTCATGG	146691
rs11871899	snp	C/G	0.396364	0.202676	intron-variant	TOM1L2	GRCh38.p7	17:17923434	caacaacaacaacaa[C/G]aacaacaaACACCCA	146691
rs12187125	snp	C/T	0	0	intron-variant	TOM1L2	GRCh38.p7	17:17911969	ATCTGTGACCTTACC[C/T]CCAACCCTGTGCTCT	146691
rs12452121	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17925815	agctatgatggtgcc[A/C]ctgtactctagcctg	146691
rs12452219	snp	C/T	0.389527	0.207442	intron-variant	TOM1L2	GRCh38.p7	17:17926109	ACAGGATGTCGAGGC[C/T]GCAGTGAGTTGTGAT	146691
rs12452254	snp	A/G	0.394904	0.203722	intron-variant	TOM1L2	GRCh38.p7	17:17926120	AGGCCGCAGTGAGTT[A/G]TGATCATACCACTGT	146691
rs12453825	snp	C/T	0.482083	0.0929373	intron-variant	TOM1L2	GRCh38.p7	17:17916321	ctcgtgatctgcctg[C/T]cttggcctcccaaag	146691
rs12600546	snp	A/G	0.455144	0.142885	intron-variant	TOM1L2	GRCh38.p7	17:17964300	TTATCTGCTAGGTCA[A/G]GAGCAACAACCCCTA	146691
rs12602500	snp	C/T	0.138546	0.223781	intron-variant	TOM1L2	GRCh38.p7	17:17966203	GGTCACCCCTCCCCT[C/T]CTACATTTCCTTACT	146691
rs12603148	snp	C/T	0.479663	0.0987666	intron-variant	TOM1L2	GRCh38.p7	17:17961943	tagcagcattattta[C/T]aatagccaaaaagtg	146691
rs12936037	snp	A/G	0.394721	0.203852	intron-variant	TOM1L2	GRCh38.p7	17:17873931	GGAGGAAAAGGTTCC[A/G]TACTTTATTTACTTA	146691
rs12940498	snp	C/G	0	0	intron-variant	TOM1L2	GRCh38.p7	17:17952469	gatcttacctcactg[C/G]agcctcgaccttccc	146691
rs12940522	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17920401	gctggagtgcagtgg[G/T]acaatctcagctcac	146691
rs12940786	snp	C/T	0	0	intron-variant	TOM1L2	GRCh38.p7	17:17921775	GGGGTGGGATTCACC[C/T]GTCCTGTCTTCCTCT	146691
rs12940832	snp	C/T	0.0479149	0.147179	intron-variant	TOM1L2	GRCh38.p7	17:17950586	ATGCTCCCATTCTAA[C/T]GAGAGTGAGTCTTGG	146691
rs12940904	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17892199	AAGACCTTTCAGGCA[G/T]AGGGAAGTGAGCACA	146691
rs12941039	snp	C/T	0.490265	0.0690849	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17862341	TAGTCAGGAAAATCT[C/T]GCTGTAAGGAATGGG	146691
rs12941550	snp	A/C	0.458315	0.13822	intron-variant	TOM1L2	GRCh38.p7	17:17850514	CAAAACAAAACAAAA[A/C]AAAAAACATGCTCCC	146691
rs12942827	snp	A/C	0	0	intron-variant	TOM1L2	GRCh38.p7	17:17966453	GCAAGAACTACAgtt[A/C]tcgaagtgaaccagt	146691
rs12942836	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17952577	tttaaatattctttg[G/T]agcaacaaggtctta	146691
rs12943087	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17952596	aacaaggtcttactg[G/T]gttgcctaggctggt	146691
rs12943500	snp	C/T	0.336474	0.234568	intron-variant	TOM1L2	GRCh38.p7	17:17887274	GACTGGATGAGATGG[C/T]TGCTAACAGAGCAGA	146691
rs12944200	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17852599	agcagggcacggtgg[C/T]tcatgcctgtaatcc	146691
rs12946283	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17852600	gcagggcacggtggc[C/T]catgcctgtaatccc	146691
rs12951376	snp	C/T	0.47517	0.10862	intron-variant	TOM1L2	GRCh38.p7	17:17849495	GCCCAGATTATATTA[C/T]CTGCTGCTGGCTCCT	146691
rs12951817	snp	A/G	0	0	intron-variant	TOM1L2	GRCh38.p7	17:17852890	aaaaaaaaaaaaaaa[A/G]gaaCATTGAATTGAA	146691
rs16960744	snp	A/G	0.464309	0.12873	intron-variant	TOM1L2	GRCh38.p7	17:17851945	AAGGTTTAAGTTGCC[A/G]TCAAATATGACATGA	146691
rs16960745	snp	C/T	0.0821764	0.185298	intron-variant	TOM1L2	GRCh38.p7	17:17867627	GATTATGTTCTGTAT[C/T]GTATTTAAAAACTCC	146691
rs16960751	snp	C/T	0.144632	0.226711	intron-variant	TOM1L2	GRCh38.p7	17:17899689	GCTCTGGGGAGCCCT[C/T]AGTCCGGCTGTGGGC	146691
rs16960766	snp	C/G	0.0130921	0.0798413	intron-variant	TOM1L2	GRCh38.p7	17:17933674	TAAAATGTTTAGCCT[C/G]GTGGAGCCATAATAG	146691
rs16960767	snp	A/G	0.0314385	0.121371	intron-variant	TOM1L2	GRCh38.p7	17:17940758	CCACAGGGTTTCAAA[A/G]GGAACAGTTTTAACT	146691
rs28366006	in-del	-/G	0.445855	0.155373	upstream-variant-2KB, intron-variant	TOM1L2, DRC3	GRCh38.p7	17:17973131	GTCTTGGCTGTCTCA[-/G]CACGACTGTAAAGTG	146691
rs28366007	snp	C/T	0.167484	0.23599	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	TOM1L2, DRC3	GRCh38.p7	17:17972903	TGGGGAACCAAGCGC[C/T]GCGACTTGGTTGCTA	146691
rs28370872	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17911665	TTTTTTTTAATTTTT[A/T]TATTTTTTATTGATC	146691
rs28421060	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17913079	GCAATCGCAGGCACT[A/C]GGCAGGCTGAGGCAG	146691
rs28428991	snp	C/T	0.455263	0.142713	intron-variant	TOM1L2	GRCh38.p7	17:17924335	TGATTGTGGTAATGG[C/T]TGAACAACGCTGTGA	146691
rs28444502	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17913057	TCAGGCGTGGCAGCG[C/G]GTGCCTGCAATCGCA	146691
rs28573153	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17913069	GCGGGTGCCTGCAAT[C/T]GCAGGCACTCGGCAG	146691
rs28584362	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17912964	CGAGGCTGGCGGATC[A/G]CTCGCGGTTAGGAGC	146691
rs28595155	snp	A/T	0.0150606	0.0854603	intron-variant	TOM1L2	GRCh38.p7	17:17886820	CACTCTGCTTCCATG[A/T]TCACAGAGACAGACT	146691
rs28642968	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17911657	ATTCTTTTTTTTTTT[A/T]AATTTTTTTATTTTT	146691
rs28680287	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17913084	CGCAGGCACTCGGCA[A/G]GCTGAGGCAGGAGAA	146691
rs28689792	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17913228	GAGGGAGAGGGAGAC[C/T]GTGGGGAGACGGGGG	146691
rs28704959	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17913051	AACCAGTCAGGCGTG[G/T]CAGCGGGTGCCTGCA	146691
rs28728241	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17912950	GCACCTCGGGAGGCC[A/G]AGGCTGGCGGATCGC	146691
rs34004233	in-del	-/A			intron-variant	TOM1L2	GRCh38.p7	17:17893440	GAGGGATGGCACCCA[-/A]GAAAGCTTCAGGAAG	146691
rs34032256	in-del	-/G			upstream-variant-2KB, intron-variant	TOM1L2, DRC3	GRCh38.p7	17:17973277	CTTTCATAGAAAGAG[-/G]AGGTACCCGGTCCAC	146691
rs34034507	in-del	-/G			intron-variant	TOM1L2	GRCh38.p7	17:17909623	GAATGGGGAGTTATT[-/G]TTTAATGAACACAGA	146691
rs34132537	in-del	-/C			intron-variant	TOM1L2	GRCh38.p7	17:17920924	CAGGTGTGAGCCACC[-/C]GTTGCAGGCAGTTCA	146691
rs34173057	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17912232	GGGGCGCCTCTGCCC[A/G]GCTGCCCCTACTGGG	146691
rs34183095	snp	A/G	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17917755	AGCTCAGGAGTTTAA[A/G]AACAGCCTGGGCAAC	146691
rs34215858	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17917636	TTCATTACATCTGTA[A/G]ATCACTTTGGGTAGT	146691
rs34240068	in-del	-/T			intron-variant	TOM1L2	GRCh38.p7	17:17872516	ACCAGAGGGAGACCT[-/T]GGCCAAAGTGTGCAG	146691
rs34249123	in-del	-/C			intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17859880	GCGAGACTCCATCTC[-/C]AAAAAAAGCAATCTG	146691
rs34289066	in-del	-/T			intron-variant	TOM1L2	GRCh38.p7	17:17899126	ACTGGACTGCCTTTT[-/T]GCAGACCTCTTGAAT	146691
rs34289357	in-del	-/G			intron-variant	TOM1L2	GRCh38.p7	17:17943487	ATGGAGAGAATGTGG[-/G]ATGATCCAAAAGAGA	146691
rs34299501	snp	A/T	0.111928	0.208413	upstream-variant-2KB, intron-variant	TOM1L2, DRC3	GRCh38.p7	17:17973179	GTCAAGCTTTTGAAT[A/T]AAAAAAAAAAAAAAT	146691
rs34308060	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17967874	CGGCCTCCCAAAGTG[A/C]TGGATTACAGGTGTG	146691
rs34317642	in-del	-/T			intron-variant	TOM1L2	GRCh38.p7	17:17881462	CACCTCCCACACTTT[-/T]GAGTCGGTGAAGGGG	146691
rs34332120	snp	C/T			intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17860229	GCTCTCTAATGCCCA[C/T]GCTGGGGCAGGTGGG	146691
rs34358059	in-del	-/T			intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17862656	AAATAAATGCCTTTT[-/T]GTGCTGGCCTGTGAC	146691
rs34367133	in-del	-/G			intron-variant	TOM1L2	GRCh38.p7	17:17967399	CTAGCCAACACAAGG[-/G]AAAACTGCAAACTGC	146691
rs34378514	in-del	-/C			intron-variant	TOM1L2	GRCh38.p7	17:17934331	TGCTCCTGTAGTCTC[-/C]AGCTACTTGGGAGGC	146691
rs34383547	in-del	-/T	0	0	intron-variant	TOM1L2	GRCh38.p7	17:17864228	TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTCGC	146691
rs34400884	in-del	-/C			intron-variant	TOM1L2	GRCh38.p7	17:17953577	GCATCACCTGGCCCC[-/C]TAACCCAGGAGGAAA	146691
rs34433429	in-del	-/AAAA			intron-variant	TOM1L2	GRCh38.p7	17:17940215	AAAAAAAAAAAAAAA[-/AAAA]GGAAGAAGAGTTCTG	146691
rs34434158	snp	C/T	0.0581099	0.160244	intron-variant	TOM1L2	GRCh38.p7	17:17966077	AGTGAGCTGAGATCG[C/T]GCCACTGCACTCCAC	146691
rs34464842	in-del	-/C			intron-variant	TOM1L2	GRCh38.p7	17:17848136	GGCAGGAACCATCCC[-/C]ACCTACCCCACCCTT	146691
rs34612894	in-del	-/C			intron-variant	TOM1L2	GRCh38.p7	17:17959052	CTTGCCCGATGAATC[-/C]TCTTCCATTTGGCTG	146691
rs34622786	in-del	-/C			intron-variant	TOM1L2	GRCh38.p7	17:17854319	AGGGAAGTGGGGCCC[-/C]TGGTTGGAGCAGGGG	146691
rs34640275	in-del	-/T			intron-variant	TOM1L2	GRCh38.p7	17:17880315	CAGGGGAGACACCTT[-/T]CCCCACCCAGCTCCC	146691
rs34681423	in-del	-/A	0	0	intron-variant	TOM1L2	GRCh38.p7	17:17875270	CAAAAAGAAAAAAAG[-/A]AAAAAAAAAAAAAAG	146691
rs34685563	in-del	-/A	0.455144	0.142885	intron-variant	TOM1L2	GRCh38.p7	17:17899949	GGCATGGTGGCTCAC[-/A]GTCTGTAATCCCAGC	146691
rs34710174	in-del	-/G			intron-variant	TOM1L2	GRCh38.p7	17:17872606	TCTGCTCTGCCATGG[-/G]ACTGTTCCGGGCCAC	146691
rs34749268	in-del	-/A			intron-variant	TOM1L2	GRCh38.p7	17:17945657	TATTTTGTGAGCAAA[-/A]GTGACCTTAATATTT	146691
rs34783062	in-del	-/C			intron-variant	TOM1L2	GRCh38.p7	17:17873834	GCTGCAGCGGCCTCC[-/C]ATGGCACGGGGCCAG	146691
rs34788344	in-del	-/C			intron-variant	TOM1L2	GRCh38.p7	17:17893488	AGAGCCATCAATTAG[-/C]AATTTCATTCCAGTG	146691
rs34865538	in-del	-/GC	0.280785	0.248097	intron-variant	TOM1L2	GRCh38.p7	17:17894975	ATACATACATACATA[-/GC]CATGCATGCATGCAT	146691
rs34879782	in-del	-/A/AA			intron-variant	TOM1L2	GRCh38.p7	17:17869309	AATCTTTTCAAGGGA[-/A/AA]AAAAAAAAAAAAAAG	146691
rs34903609	in-del	-/A			intron-variant	TOM1L2	GRCh38.p7	17:17955487	GGATTACAGGCACAC[-/A]GCCACCAAGCCCAGA	146691
rs34912631	in-del	-/G			intron-variant	TOM1L2	GRCh38.p7	17:17941733	GCAATTTTACAGTGG[-/G]AAATGGATACATAAG	146691
rs34967526	in-del	-/AC			intron-variant	TOM1L2	GRCh38.p7	17:17945291	CACACACACACACAC[-/AC]TCTCTCTCTCTCTCT	146691
rs34991179	in-del	-/G			intron-variant	TOM1L2	GRCh38.p7	17:17880729	TTTCCTCACCTACAG[-/G]AAAGGTGGCACTAAC	146691
rs35006161	in-del	-/T			intron-variant	TOM1L2	GRCh38.p7	17:17965321	GCCTTATCCTCCCTT[-/T]CCCAGTCTCACCCCC	146691
rs35007355	in-del	-/C			intron-variant	TOM1L2	GRCh38.p7	17:17876376	CTGCCTATCCCTCCC[-/C]TGTGGTGGGCTGCGA	146691
rs35022332	in-del	-/T			intron-variant	TOM1L2	GRCh38.p7	17:17962325	GGTGATTGTTGCATA[-/T]TTTTTTTTTTTTAGG	146691
rs35040991	in-del	-/T			intron-variant	TOM1L2	GRCh38.p7	17:17969682	CTTCACAGGTCACAG[-/T]ACGGGCCAGTTGTTT	146691
rs35052993	in-del	-/C			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17843904	CGCAGGGGAAGCCTG[-/C]ACTTGGACCCCACAG	146691
rs35098604	in-del	-/C			intron-variant	TOM1L2	GRCh38.p7	17:17898412	AAGCTCACCACTCCC[-/C]TGTTTCAGAGGACAG	146691
rs35146679	in-del	-/C			intron-variant	TOM1L2	GRCh38.p7	17:17905004	GCTATACCTCCACCC[-/C]TGGGGGTCAGTAAAC	146691
rs35149306	in-del	-/G			intron-variant	TOM1L2	GRCh38.p7	17:17887115	ACCTGGACTTCTGGG[-/G]AGACTCTGCCCTGTC	146691
rs35150040	in-del	-/A			intron-variant	TOM1L2	GRCh38.p7	17:17889481	CCCCTTCCCCTCAAT[-/A]CTGGCTGCAGCTCTG	146691
rs35159529	in-del	-/C			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17845459	GCACTATGGAATCCC[-/C]TGCTCCTTTCAGAGC	146691
rs35222539	in-del	-/A	0	0	intron-variant	TOM1L2	GRCh38.p7	17:17855975	AAGAAAAAAAAAAAA[-/A]CAAACTGCAGTCAGT	146691
rs35408977	in-del	-/T			intron-variant	TOM1L2	GRCh38.p7	17:17865762	TTTTTTTTTTTTTTT[-/T]GAGACAGTGTCTTGC	146691
rs35415447	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17962824	AATTTAGCTGGGCGT[A/G]GTGGCGCGTGCCTGT	146691
rs35451946	snp	C/G	0.463234	0.130503	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17860747	TTTGTTAGGCAAAAA[C/G]AAAAATCTCATGAGA	146691
rs35508354	in-del	-/TA			intron-variant	TOM1L2	GRCh38.p7	17:17942490	AAATCATATCAATTT[-/TA]AAAGGACATTTATAA	146691
rs35540485	in-del	-/C			intron-variant	TOM1L2	GRCh38.p7	17:17848651	TAAATCACACTTCCC[-/C]AAATCAGCGTAAGAC	146691
rs35563098	in-del	-/C			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17846296	CAGCGAGCTGGGCCC[-/C]AAGACACACGGGGAT	146691
rs35579807	in-del	-/A/AA			intron-variant	TOM1L2	GRCh38.p7	17:17885925	AAAAAAAAAAAAAAA[-/A/AA]ATTCTGTTCTTTGGA	146691
rs35590413	in-del	-/G			intron-variant	TOM1L2	GRCh38.p7	17:17878624	GTGTAGCACTTGGGG[-/G]ACCAAGACTGACAAC	146691
rs35600233	in-del	-/T			intron-variant	TOM1L2	GRCh38.p7	17:17897943	TTTTTTTTTTTTTTT[-/T]GAGACGAAGTCTCAC	146691
rs35622054	snp	A/G/T	0.00636936	0.0560724	intron-variant	TOM1L2	GRCh38.p7	17:17865784	GTGTCTTGCTCTGTC[A/G/T]CCCAGGCTGGAGTGC	146691
rs35633724	in-del	-/G			intron-variant	TOM1L2	GRCh38.p7	17:17934382	GCCCGGGGATCAAGG[-/G]CTGCAGTGAGCTATG	146691
rs35668837	in-del	-/G			intron-variant	TOM1L2	GRCh38.p7	17:17910839	TCCCAAAGTGCTGGG[-/G]ATTACAGGCGTGAGC	146691
rs35672484	in-del	-/TT			intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17858235	CTACATTTTTTTTTT[-/TT]CTCTTTTCTAGTGGC	146691
rs35723284	in-del	-/CT	0.396364	0.202676	intron-variant	TOM1L2	GRCh38.p7	17:17852118	TTACAAAAATGCCAG[-/CT]CTGTCTATAGCTGGC	146691
rs35745427	in-del	-/C			intron-variant	TOM1L2	GRCh38.p7	17:17940722	GTCATTGGGGTGACC[-/C]TCGCTAATTCAAATA	146691
rs35769010	in-del	-/A			intron-variant	TOM1L2	GRCh38.p7	17:17886011	AGGCCTTCCCAGAAA[-/A]TGGCCCTTCTCATGC	146691
rs35798490	in-del	-/G			intron-variant	TOM1L2	GRCh38.p7	17:17946411	ACTAATCTGCCTTTT[-/G]CTCTATATAGATGTG	146691
rs35832741	in-del	-/G			intron-variant	TOM1L2	GRCh38.p7	17:17964851	TAGAAAAGCCCTGGG[-/G]AATAGGTCAGCCCTG	146691
rs35903499	in-del	-/G			intron-variant	TOM1L2	GRCh38.p7	17:17872155	CCAACAACACAGGGG[-/G]AAACACTCATTACAG	146691
rs35975670	in-del	-/T			intron-variant	TOM1L2	GRCh38.p7	17:17951845	CAACCAAATGCCTTT[-/T]CCCCTCCTCAGATGT	146691
rs35985348	snp	A/G	0.0146672	0.084371	intron-variant	TOM1L2	GRCh38.p7	17:17911513	GTTTTGACGATTTAG[A/G]TGACAAAATAAATGA	146691
rs35991536	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17917731	AGGCCAAGGTGGGAA[A/G]ACTGCTTGAGCTCAG	146691
rs36019227	in-del	-/C			intron-variant	TOM1L2	GRCh38.p7	17:17916772	CACGCCTGTAATCCC[-/C]GATACTTTGGGAGGC	146691
rs36029602	in-del	-/C			intron-variant	TOM1L2	GRCh38.p7	17:17911414	TACAATTATCCGTCC[-/C]AGAGGGCTGGCTGGT	146691
rs36043265	in-del	-/G			intron-variant	TOM1L2	GRCh38.p7	17:17947216	TATACGGTGGGGGGG[-/G]TCTCACTATATTGCC	146691
rs36050958	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17917820	ATTAGCCAGGAGTGG[G/T]GGCTTACACCTGTCA	146691
rs36079750	in-del	-/C			intron-variant	TOM1L2	GRCh38.p7	17:17899237	GAGAAACCATATGAG[-/C]AGACACAGAAGAGAG	146691
rs36095502	in-del	-/A	0.455024	0.143057	intron-variant	TOM1L2	GRCh38.p7	17:17962233	AAAATGGTAGTTGCC[-/A]GGGGCTGGGGGGAGG	146691
rs55784499	snp	C/T	0.0138799	0.0821421	intron-variant	TOM1L2	GRCh38.p7	17:17852229	ATGTAAAAAATAACA[C/T]GACCTTCACAAAGAA	146691
rs55850617	snp	A/G			intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17859647	GCACTTTGGGAGGCC[A/G]AGACGGGCAGAGTGC	146691
rs55930046	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17903833	GGGAAATGAGATTCA[A/G]ACTGAGAGATCCAGT	146691
rs56153053	snp	A/G	0.0704125	0.17392	intron-variant	TOM1L2	GRCh38.p7	17:17921443	TATTTGATGTATGCC[A/G]TTCTTTGTACTTAAT	146691
rs56160247	snp	C/T	0.0741063	0.177655	intron-variant	TOM1L2	GRCh38.p7	17:17884566	GCAGCAGCAGAAGGG[C/T]GGCTGCAGCAGCTTG	146691
rs56232485	snp	C/T	0.0391387	0.134304	intron-variant	TOM1L2	GRCh38.p7	17:17909349	AAGGTGTAAACAGCC[C/T]GTGTCCATCAATTAA	146691
rs56677911	in-del	-/A			intron-variant	TOM1L2	GRCh38.p7	17:17898891	GCAAAAAAGAATAAA[-/A]GAAACTCATGCACCA	146691
rs56698800	snp	C/T	0.0205511	0.0992634	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17858344	GGTCTCACTGTGTTG[C/T]CCGGACTGGTCTCAA	146691
rs56758399	snp	C/T	0.0115144	0.0749975	intron-variant	TOM1L2	GRCh38.p7	17:17906105	CCTTCTAAATGAGAC[C/T]TTTCTGTTGTTTTGT	146691
rs56886154	snp	A/C	0.387263	0.208947	intron-variant	TOM1L2	GRCh38.p7	17:17928159	AATTTTCTGTAACAA[A/C]AAAAAAAATCAGTAG	146691
rs56928492	snp	C/T	0.0766824	0.180169	intron-variant	TOM1L2	GRCh38.p7	17:17856955	TCTGTTTCTACTGTG[C/T]TTATTTTTTTATTTT	146691
rs57006959	snp	C/T	0.151668	0.229849	intron-variant	TOM1L2	GRCh38.p7	17:17848192	TGCTGAGGAATGCAG[C/T]GGGGAGGGGGGAGTG	146691
rs57082481	snp	C/T	0.0368353	0.130617	intron-variant	TOM1L2	GRCh38.p7	17:17948952	TGCTCAGAGTAAGTA[C/T]TGGGCAAAGCCAAAA	146691
rs57147966	in-del	-/AACAAA			intron-variant	TOM1L2	GRCh38.p7	17:17924150	TCAAACAAAAACAAA[-/AACAAA]GGTAAAAATGACTAC	146691
rs57262667	snp	C/T	0.150333	0.229274	intron-variant	TOM1L2	GRCh38.p7	17:17865805	GCTGGAGTGCAATGA[C/T]GCGATATCGGCTCAC	146691
rs57277459	snp	A/G	0.0387552	0.1337	intron-variant	TOM1L2	GRCh38.p7	17:17900498	CTGCACTCCAGCCTG[A/G]GTGACAGAGTAAGAC	146691
rs57323732	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17863819	CTCCCAAAGTGATGA[A/G]ATTGCAAGTGTGAGC	146691
rs57451875	in-del	-/GCATGGTAG			intron-variant	TOM1L2	GRCh38.p7	17:17917686	AGCTTCCCAGGCCAG[-/GCATGGTAG]CTCATGCCTGTAAAT	146691
rs57525532	in-del	-/AT	0.0622301	0.165053	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17843665	TGCCCACAGAAACAC[-/AT]GACAGTGACAAAAAC	146691
rs57599370	in-del	-/AA			intron-variant	TOM1L2	GRCh38.p7	17:17926192	AAAAAAAAAAAAAAA[-/AA]GCTAGGTACAAGCTT	146691
rs57728924	snp	A/G	0.445592	0.155704	intron-variant, upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17972028	CGTGAGGTGGCACCG[A/G]CGCCCAGTGAAGGCC	146691
rs57770081	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17904567	TAACCTAAGTGCCTG[C/T]GAAACCCCTGAAGGC	146691
rs57791826	snp	C/T	0.0322114	0.122752	intron-variant	TOM1L2	GRCh38.p7	17:17898446	AACCCAAAGGCAATA[C/T]CAGAAGGCTTTGCTG	146691
rs57878351	in-del	-/T			intron-variant	TOM1L2	GRCh38.p7	17:17847937	TCGTGAGCTGCAGTG[-/T]TGGGGGGAGGCTCCT	146691
rs57964957	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17875934	GGCCTTGGCCGTTCT[A/G]TCTTTGTTGAAATGA	146691
rs57969260	snp	A/C	0.00478085	0.0486577	intron-variant	TOM1L2	GRCh38.p7	17:17915682	CACCACAACTAGATA[A/C]TTTTCTTTAAAAAAA	146691
rs58016787	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17955223	TTCTCTCCACCTCTT[C/T]TATCATACTCAGCAG	146691
rs58018883	snp	A/G	0.0596104	0.162024	intron-variant	TOM1L2	GRCh38.p7	17:17853005	ATGACTGACAGATGT[A/G]TTAACAATGCCTAAG	146691
rs58066258	snp	C/T	0.132409	0.220618	intron-variant	TOM1L2	GRCh38.p7	17:17865525	GGGACTACAGGTGCC[C/T]GCCACCAAGTCTGGC	146691
rs58166931	in-del	-/C	0.0189856	0.0955633	intron-variant	TOM1L2	GRCh38.p7	17:17868007	GGCTTTGCCTCTGAA[-/C]TTATGTGTAATGCTT	146691
rs58219643	snp	A/G	0.0770498	0.180522	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17858480	GGAGTGCAGTGGTGC[A/G]ATCTCGGCTCACTGC	146691
rs58249969	snp	G/T	0.00517822	0.0506191	intron-variant	TOM1L2	GRCh38.p7	17:17868916	TTTTTTCTTTTTTTT[G/T]AAGATGGGAAAGAGG	146691
rs58376085	snp	A/G/T	0.0704125	0.17392	intron-variant	TOM1L2	GRCh38.p7	17:17922850	GGGTGACTGTCTCCA[A/G/T]TGCTTTTATTGCAGC	146691
rs58495771	in-del	-/C	0.130008	0.219321	intron-variant	TOM1L2	GRCh38.p7	17:17878510	TCACCCCCATAAGAG[-/C]CGATGGCTTTGGAGT	146691
rs58628558	snp	C/T	0.0607341	0.163335	intron-variant	TOM1L2	GRCh38.p7	17:17855433	ATTTTCCTGGCTGCA[C/T]CCTGCAAAAGGGAGA	146691
rs58881326	in-del	-/ATTATT			intron-variant	TOM1L2	GRCh38.p7	17:17904011	ATTATTATTATTATT[-/ATTATT]TTTAAGATATGGGGT	146691
rs58936409	snp	G/T	0.0704125	0.17392	intron-variant	TOM1L2	GRCh38.p7	17:17903921	GAGGCCTTCAGGGAG[G/T]GCACAAAGGGGTGGG	146691
rs58957900	snp	A/G	0.134119	0.221521	intron-variant	TOM1L2	GRCh38.p7	17:17923675	AGCCTGGGCAAGAGG[A/G]TGAGACCCCATCTCA	146691
rs59015453	in-del	-/GT			intron-variant	TOM1L2	GRCh38.p7	17:17891820	TGTGTGTGTGTGTGT[-/GT]CAGAGGGAGACAGAG	146691
rs59297123	in-del	-/A	0.377187	0.215229	intron-variant	TOM1L2	GRCh38.p7	17:17906132	TTGTCTTCTCTTTTC[-/A]TTTTTTTTTTTTTTG	146691
rs59304093	snp	A/G	0.445592	0.155704	intron-variant, upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17972093	GCACAAGCGCCCGGC[A/G]AAGGCCCGACGACCA	146691
rs59334660	snp	A/T	0.126564	0.217402	intron-variant	TOM1L2	GRCh38.p7	17:17898161	GAACTCCTGACCTTG[A/T]GATCCTCCCGCTTCA	146691
rs59382992	in-del	-/CCCTG			intron-variant	TOM1L2	GRCh38.p7	17:17911305	CTCAGGCCTGCCCTG[-/CCCTG]TCCAGTCCAGCCCAG	146691
rs59445408	snp	A/G	0.0205511	0.0992634	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17858615	TTGAGATGGAGTCTA[A/G]CTCTGTCGCCAGGCT	146691
rs59692932	snp	A/C/G	0.00358779	0.0422022	intron-variant	TOM1L2	GRCh38.p7	17:17906286	GGTGTGCACCACCAC[A/C/G]CCTGGCTAACTTTTG	146691
rs59713490	snp	C/T	0.124491	0.216211	intron-variant	TOM1L2	GRCh38.p7	17:17848298	CAGGGTCTGGCAGAC[C/T]TGGGGAGAGGAGGAC	146691
rs59751059	snp	A/G/T	0.0119174	0.076348	intron-variant	TOM1L2	GRCh38.p7	17:17909842	GACAACAGCTTGGGC[A/G/T]ACATAGCAAGACATT	146691
rs59899858	snp	A/C	0.0607341	0.163335	intron-variant	TOM1L2	GRCh38.p7	17:17855277	GGGGTTAGGATTATC[A/C]TTCCAGAGTAAGAGC	146691
rs59929025	snp	A/G	0.0603597	0.1629	intron-variant	TOM1L2	GRCh38.p7	17:17940512	CATGCCATAGCCAGG[A/G]GAGAGTCCTGTGGGT	146691
rs59948477	snp	C/G	0.093777	0.195178	intron-variant	TOM1L2	GRCh38.p7	17:17915780	TCTTGCCTTGGCCCC[C/G]CAAAGTACTAGGATC	146691
rs60045046	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17881870	TATCCCTACACACAC[A/G]TTGCTTGACCCCTCT	146691
rs60073596	snp	G/T	0.482384	0.0921818	intron-variant	TOM1L2	GRCh38.p7	17:17967660	CATTCAGGCTGGAGT[G/T]CAAATGGCACGATCT	146691
rs60388742	in-del	-/TTTTTT			intron-variant	TOM1L2	GRCh38.p7	17:17952404	TTTTTTTTTTTTTTT[-/TTTTTT]GAGACAGGATTTCAC	146691
rs60604370	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17852549	TGTTGCTCATTATTT[C/T]TTTGACTTACTGGGG	146691
rs60743050	snp	A/T	0.0581099	0.160244	intron-variant	TOM1L2	GRCh38.p7	17:17898431	TTCAGAGGACAGGAA[A/T]ACCCAAAGGCAATAC	146691
rs60749449	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17964516	ACAAATTTGTGAGGA[C/T]GCACATTGTGGAGAT	146691
rs61050785	snp	C/T	0.0704125	0.17392	intron-variant	TOM1L2	GRCh38.p7	17:17936515	GTAAATAATCTGAAA[C/T]GCAAAGATATAAGCC	146691
rs61169324	snp	A/G	0.132409	0.220618	intron-variant	TOM1L2	GRCh38.p7	17:17857140	TTGTATTTTTAGTAG[A/G]GACAGGGTTTCACCA	146691
rs61188141	snp	C/T	0.0322114	0.122752	intron-variant	TOM1L2	GRCh38.p7	17:17873134	CCTTATTTCCTTTTC[C/T]ATCAAACAAACTCTT	146691
rs61217632	snp	C/T	0.211212	0.246973	intron-variant	TOM1L2	GRCh38.p7	17:17872392	GGGCTGACAGAGGAG[C/T]ACAGATTTAGGTTAA	146691
rs61225351	snp	C/G	0.0618563	0.164627	intron-variant	TOM1L2	GRCh38.p7	17:17876230	CAGATGCAGTGTCTT[C/G]AATTTCGGGCCCAGA	146691
rs61501350	snp	G/T	0.00953873	0.0683987	intron-variant	TOM1L2	GRCh38.p7	17:17955345	TTTTTTTTTTTTTTT[G/T]TTTTTGTTTTTGAGA	146691
rs61555188	snp	A/G	0.0770498	0.180522	intron-variant	TOM1L2	GRCh38.p7	17:17912566	CGGCGGGGCAGAGGC[A/G]CTCCCCACATCTCAG	146691
rs61657399	snp	G/T	0.127599	0.217986	intron-variant	TOM1L2	GRCh38.p7	17:17926886	AAAGAAAAAGAAAAA[G/T]AAATGTAACCATATT	146691
rs61679820	snp	A/C	0.0581099	0.160244	intron-variant	TOM1L2	GRCh38.p7	17:17872146	CACAGGAAAACCAAC[A/C]ACACAGGGGAAACAC	146691
rs62064120	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17851142	AGATGGCAGGTGAGG[A/G]AAGCAATGAGGTGCA	146691
rs62064155	snp	C/G	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17905536	TCCTCACTGGGTTTT[C/G]TTTCTTCTTTTTTCT	146691
rs62064156	snp	C/T	0.387453	0.208822	intron-variant	TOM1L2	GRCh38.p7	17:17919166	CCTTTTGGACTGCTG[C/T]AAAATGCTGCAATAA	146691
rs62064157	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17920230	TTCTTTTTTTTTTTA[A/T]TTAATACATCTTTTA	146691
rs62064158	snp	C/T	0.455263	0.142713	intron-variant	TOM1L2	GRCh38.p7	17:17923621	CTTGAGGCTAGGAGG[C/T]CAAGGCTACAGTGAG	146691
rs62072024	snp	G/T	0.00597247	0.0543191	intron-variant	TOM1L2	GRCh38.p7	17:17929297	CTGCTTAGAGCTGCT[G/T]TGAGCAGCAGGCTTT	146691
rs62072025	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17934770	CATCCAAAGCAAGGG[A/C]ATGACTGTGTATGCA	146691
rs62072026	snp	C/T	0.00478085	0.0486577	intron-variant	TOM1L2	GRCh38.p7	17:17935791	CAGTTGGCAAATCAA[C/T]CTAAAAATATTCAAC	146691
rs62072044	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17959750	AGCCCAATTCTCTGA[A/G]ATGAAAGAATCAGTC	146691
rs62072046	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17969075	TTTTTTTTTTTTTTG[G/T]AGACAGAGTCTCACT	146691
rs62072047	snp	A/C	0.0236746	0.106192	intron-variant	TOM1L2	GRCh38.p7	17:17969223	CACCACACCCGGCTC[A/C]TTTTTGTATTACTAG	146691
rs63721860	snp	C/T	0.479984	0.0980171	intron-variant	TOM1L2	GRCh38.p7	17:17926262	CTGAACATACAGACT[C/T]AAGGATAAAAGCCTG	146691
rs66531105	snp	C/T	0.455263	0.142713	intron-variant	TOM1L2	GRCh38.p7	17:17905687	GGGATTGCAGGTGCA[C/T]GCCACTATGCCAGGC	146691
rs66943513	in-del	-/C			upstream-variant-2KB, intron-variant	TOM1L2, DRC3	GRCh38.p7	17:17973132	ACTTTACAGTCGTGT[-/C]GAGACAGCCAAGACA	146691
rs67253360	snp	C/T	0.455383	0.142541	intron-variant	TOM1L2	GRCh38.p7	17:17925659	CCAGCCTGGCCAACA[C/T]AGCGACCTCACCTCG	146691
rs67325661	snp	A/T	0.444444	0.157135	intron-variant	TOM1L2	GRCh38.p7	17:17906132	TTGTCTTCTCTTTTC[A/T]TTTTTTTTTTTTTTG	146691
rs67575563	in-del	-/A	0.375	0.216506	intron-variant	TOM1L2	GRCh38.p7	17:17955350	TCTTGTCTCAAAAAC[-/A]AAAAAAAAAAAAAAA	146691
rs71155307	in-del	-/A	0	0	intron-variant	TOM1L2	GRCh38.p7	17:17917480	AAGACCCTGTCTCTG[-/A]AAAAAAAAAAAAAAA	146691
rs71355556	in-del	-/A	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17890872	AAAAGTTTAAAAAAA[-/A]GAAAGGGCTAGGGAT	146691
rs71355557	in-del	-/C	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17921779	TGGGATTCACCTGTC[-/C]TGTCTTCCTCTCGGC	146691
rs71367417	snp	C/T	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17848440	CATCCAGCCCATCAG[C/T]TGAGGCCCAGGAGAG	146691
rs71367418	snp	C/T	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17877015	GTTGCTGTGTTCACT[C/T]TGGGCACCCTTCCTT	146691
rs71367419	snp	C/T	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17886067	AGGAGGAGGCAGAGC[C/T]TCCTGTGCCCATGAC	146691
rs71367420	snp	A/G	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17906577	TACTCTAGACTGGCC[A/G]CTCCCCAAGGGGAAG	146691
rs71367421	snp	C/G	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17913259	AGACCGTGGGGAGAC[C/G]GGAGAGGGAGAGGGA	146691
rs71367422	snp	A/G	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17917104	GGCAGAGGTTGCAAT[A/G]AGCCGAGATCACGCC	146691
rs71367423	snp	A/G	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17917483	TTTTTTTTTTTTTCA[A/G]AGACAGGGTCTTGCT	146691
rs71367424	snp	C/T	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17925584	CAGTGGCTCATGCCT[C/T]TAATCCCAGCACTTT	146691
rs71367425	snp	A/T	0.0138799	0.0821421	intron-variant	TOM1L2	GRCh38.p7	17:17926089	GGTGAGAGGATCACT[A/T]GAGCACAGGATGTCG	146691
rs71367426	snp	C/T	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17927779	AGTGAGCCTCCCACC[C/T]TCAGCCTCCTGAGTA	146691
rs72838921	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17858412	CCTGAGTAGCTAGAA[C/T]GACTTTTTCTTTTTC	146691
rs72838939	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	TOM1L2, DRC3	GRCh38.p7	17:17974070	TGAGAAACACTGTGA[A/G]CTGTGGCAATGATAG	146691
rs73299846	snp	A/G	0.089084	0.191327	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17844595	TGCACGCTGGTAAGC[A/G]AGCCAGTCATTCTCT	146691
rs73299861	snp	A/G	0.0329836	0.124112	intron-variant	TOM1L2	GRCh38.p7	17:17857311	TGGATATAAGCAACT[A/G]TATTATAAAAATCTG	146691
rs73299869	snp	G/T	0.150333	0.229274	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17859812	CTTGAACCTGGGAGA[G/T]GAAAGCTGCAGTGAG	146691
rs73299873	snp	A/C	0.0770498	0.180522	intron-variant	TOM1L2	GRCh38.p7	17:17863122	CAAGGCAGGGACTGG[A/C]GCCAGTGCACCTGCA	146691
rs73299885	snp	C/T	0.148996	0.228688	intron-variant	TOM1L2	GRCh38.p7	17:17881159	AGATGGTCTGGGTCC[C/T]GAGAGGCTCTTGTTA	146691
rs73299887	snp	A/G	0.093417	0.194889	intron-variant	TOM1L2	GRCh38.p7	17:17884050	AGCTGCCCCCTCCAC[A/G]GTGCTCAAGTTACTG	146691
rs73299892	snp	A/G	0.031825	0.122064	intron-variant	TOM1L2	GRCh38.p7	17:17888485	TTTGGATAGAAGGGA[A/G]CTTCTGTCAGCTCCT	146691
rs73299893	snp	C/G	0.0599851	0.162463	intron-variant	TOM1L2	GRCh38.p7	17:17890063	TGGGAGCAGCACTTT[C/G]TCTCCTGGGGGAATT	146691
rs73301821	snp	C/T	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17919722	CTACCATTGAACCAC[C/T]GGTCTCAAGTCTTCA	146691
rs73301827	snp	C/T	0.0387552	0.1337	intron-variant	TOM1L2	GRCh38.p7	17:17921952	CCACACTGTCACCAG[C/T]CTTTTTTTTGAGCTT	146691
rs73301842	snp	C/T	0.093417	0.194889	intron-variant	TOM1L2	GRCh38.p7	17:17925136	AGAAGCAGCTGCCAG[C/T]ACTATGCTTCCTATA	146691
rs73301851	snp	C/T	0.093417	0.194889	intron-variant	TOM1L2	GRCh38.p7	17:17926320	TTTATTCTGACCAGG[C/T]CTCCCTGCTAACTCT	146691
rs73301854	snp	A/G	0.093417	0.194889	intron-variant	TOM1L2	GRCh38.p7	17:17927971	GAAATGCATACTTAG[A/G]TATTCATAGATGAAA	146691
rs73301859	snp	C/T	0.0337553	0.125452	intron-variant	TOM1L2	GRCh38.p7	17:17931193	ACATCCCCACCTTTT[C/T]GTTACTACCTATTTT	146691
rs73301862	snp	A/G	0.0577344	0.159793	intron-variant	TOM1L2	GRCh38.p7	17:17931697	TTTGGAATTAGATCA[A/G]AGAGTCTGACATGCA	146691
rs73301865	snp	A/C	0.093417	0.194889	intron-variant	TOM1L2	GRCh38.p7	17:17934491	CTAGGCAAAGGAACA[A/C]AGCCTGAAAGGCTAG	146691
rs73301873	snp	C/G	0.093417	0.194889	intron-variant	TOM1L2	GRCh38.p7	17:17939473	CAATCACAGTATTGT[C/G]ATTGTTTCTAAAATG	146691
rs73301880	snp	C/T	0.093417	0.194889	intron-variant	TOM1L2	GRCh38.p7	17:17941939	GTCCAACCTGGACAA[C/T]ACAGCAAGACCTCAT	146691
rs73301894	snp	A/T	0.0372196	0.131242	intron-variant	TOM1L2	GRCh38.p7	17:17953016	CGCCATGCCCAACAG[A/T]CTGGTCCCCACCCCT	146691
rs73301900	snp	A/G	0.0770498	0.180522	intron-variant	TOM1L2	GRCh38.p7	17:17956079	ACATTTGTTTCAAAG[A/G]GCAAAAGAACAAAGC	146691
rs73303809	snp	C/T	0.0599851	0.162463	intron-variant	TOM1L2	GRCh38.p7	17:17959083	TTGCTGAGTTATATC[C/T]TTTGTCACGAAAATG	146691
rs73303812	snp	C/G	0.0322114	0.122752	intron-variant	TOM1L2	GRCh38.p7	17:17961312	CCTATAATCCCAACA[C/G]TTTGGGAGGCCAAGA	146691
rs73303813	snp	C/T	0.0244538	0.107838	intron-variant	TOM1L2	GRCh38.p7	17:17961488	ACTAAGGCAGGAGGA[C/T]TGCTCGAGTTCAGAA	146691
rs73303821	snp	C/T	0.0936653	0.195088	intron-variant	TOM1L2	GRCh38.p7	17:17965042	TCTGAGGGGGCTTCA[C/T]AGACAGTGTCCCTAC	146691
rs73303826	snp	A/G	0.00874735	0.0655527	intron-variant	TOM1L2	GRCh38.p7	17:17967361	AAACTTTACTCTTGG[A/G]AAAGGATTTTCTGAA	146691
rs73303830	snp	C/T	0.093417	0.194889	intron-variant	TOM1L2	GRCh38.p7	17:17969014	CTTCTCTCCTGAAAC[C/T]GTAAATCCATTGAGG	146691
rs73303831	snp	A/G	0.093417	0.194889	intron-variant	TOM1L2	GRCh38.p7	17:17969514	TTGTCACAACAGTAC[A/G]GAATATACATTAGAA	146691
rs73303833	snp	C/T	0.0314385	0.121371	intron-variant	TOM1L2	GRCh38.p7	17:17970365	CACCGCACCCAACCA[C/T]ATTTGTATTTTAAAT	146691
rs73979206	snp	C/G	0.0193772	0.0965046	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17846916	CACCATCTGCGGGCT[C/G]CCTGCTGCCCTCCCA	146691
rs73979207	snp	A/G	0.0360663	0.129354	intron-variant	TOM1L2	GRCh38.p7	17:17853768	CCCACTTTCTTCACC[A/G]GAGAGCTCCTGAGTT	146691
rs73979209	snp	C/T	0.151668	0.229849	intron-variant	TOM1L2	GRCh38.p7	17:17862939	AGGACGCCAGCCAGG[C/T]GGGTTTAGGTTCCAT	146691
rs73979211	snp	C/G	0.0755793	0.179102	intron-variant	TOM1L2	GRCh38.p7	17:17867905	ACAATTTTAATCCTG[C/G]GGTACCTTTCCCACA	146691
rs73979217	snp	C/T	0.0387552	0.1337	intron-variant	TOM1L2	GRCh38.p7	17:17896510	GCCTGGTCTTGGAAG[C/T]GCCCTGGACAGAGAT	146691
rs73979241	snp	A/G	0.0150606	0.0854603	intron-variant	TOM1L2	GRCh38.p7	17:17937358	AGGAAATGGTAGCCT[A/G]TGTGCCAATATCCAC	146691
rs73979242	snp	A/C	0.0197687	0.0974348	intron-variant	TOM1L2	GRCh38.p7	17:17943854	AGGGCCCCACGTGAA[A/C]ATCCAGAGCCCAAGG	146691
rs73979243	snp	C/T	0.0696718	0.173152	intron-variant	TOM1L2	GRCh38.p7	17:17951631	AAACCTTTCAAGAAA[C/T]GTAAAGGTCTTGCAT	146691
rs74255341	snp	C/T	0.0158469	0.0875917	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17859435	TCATTTCGAGGTCAG[C/T]ATGGCTTGGGATGGG	146691
rs74336194	snp	C/T	0.0023933	0.0345097	intron-variant	TOM1L2	GRCh38.p7	17:17931590	ACAAAATGAGCTCCT[C/T]GAAAGGCAATACAAT	146691
rs74411723	snp	A/G	0.0325976	0.123435	intron-variant	TOM1L2	GRCh38.p7	17:17952283	CTTCATGGAACATGC[A/G]CCACACACTAAGCAG	146691
rs74417974	snp	C/G	0.0391387	0.134304	intron-variant	TOM1L2	GRCh38.p7	17:17885576	CACAGAGAGGAAAGA[C/G]CAAAAATTCAAGTAG	146691
rs74433088	snp	A/G	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17912128	TTTCTATTCCACAAA[A/G]CCGCCACTGTCATCA	146691
rs74440715	snp	A/G	0.0162398	0.0886349	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17845065	GAGCAGAGATCTCAG[A/G]ACAGGCCATCTCGCC	146691
rs74473167	snp	A/G	0.0174175	0.0916809	intron-variant	TOM1L2	GRCh38.p7	17:17890610	CTAGAATCACAGGCA[A/G]CAATGCGTGTGACAC	146691
rs74488035	snp	A/G	0.0414363	0.137845	intron-variant	TOM1L2	GRCh38.p7	17:17950851	GTAGTCCCCAGGAGA[A/G]TGGAAACTGCAAGAT	146691
rs74500432	snp	C/T	0.00874735	0.0655527	intron-variant	TOM1L2	GRCh38.p7	17:17964166	ACATATGTAACCAAG[C/T]CTGAGACTGGTTTTA	146691
rs74506959	snp	A/C	0.00597247	0.0543191	intron-variant	TOM1L2	GRCh38.p7	17:17894160	ACTCCTCTCTCTGGG[A/C]CTCTGGGTATAAGGC	146691
rs74528549	snp	A/G	0.16618	0.23553	intron-variant	TOM1L2	GRCh38.p7	17:17882455	GCATGTCAGGTCCCC[A/G]GTGCCTCCCAGGCAC	146691
rs74573174	snp	A/T	0.0618563	0.164627	intron-variant	TOM1L2	GRCh38.p7	17:17955008	GCAATGTCTTTATGT[A/T]CAAAAAGCATTTATG	146691
rs74582416	snp	A/T	0.0174175	0.0916809	intron-variant	TOM1L2	GRCh38.p7	17:17928289	TGAGAAAAACACTGC[A/T]GCTCCCAACAAACGA	146691
rs74585069	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17892071	CAAAGCCAGTCTTGA[A/G]GACCACAAAAAAGGA	146691
rs74786790	snp	C/T	0.0618563	0.164627	intron-variant	TOM1L2	GRCh38.p7	17:17946669	CATGGGTGCAGAGGC[C/T]GCAGGAGGCCTGTTT	146691
rs74790591	snp	G/T	0.00636936	0.0560724	intron-variant	TOM1L2	GRCh38.p7	17:17966539	AAACCTACTGAAACA[G/T]AAACTCTGAGGGTAG	146691
rs74887979	snp	A/T	0.00953873	0.0683987	intron-variant	TOM1L2	GRCh38.p7	17:17934608	GGGATAATTTCTAAA[A/T]TTTTTCTCCTAAAAA	146691
rs74912104	snp	A/C	0.0391387	0.134304	intron-variant	TOM1L2	GRCh38.p7	17:17869115	TTACAAAGGGCAGAG[A/C]CTAATTCTGCACGTC	146691
rs74995486	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17901390	CTAGCAGCTTTCAGG[A/G]GAAAGGTCAGGCTCC	146691
rs75053299	snp	C/G	0.0325976	0.123435	intron-variant	TOM1L2	GRCh38.p7	17:17947211	CAGTTTTATACGGTG[C/G]GGGGGTCTCACTATA	146691
rs75090450	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17903764	CATCAGTACAACACG[A/G]GTTATGAAATCATAT	146691
rs75114179	snp	C/T	0.0168055	0.0901129	intron-variant	TOM1L2	GRCh38.p7	17:17963858	GAATCAAGAAGTCTA[C/T]ATTAGTTGATTGCAG	146691
rs75118126	snp	C/T	0.0325976	0.123435	intron-variant	TOM1L2	GRCh38.p7	17:17958570	CCCTCCCTGCCCATA[C/T]ACAAATATCTAAATG	146691
rs75134216	snp	A/T	0.0197687	0.0974348	intron-variant	TOM1L2	GRCh38.p7	17:17892169	AGGAGGAGTCACTGC[A/T]CTGAAAGCTGGGGAA	146691
rs75169217	snp	C/G	0.0441095	0.141807	intron-variant	TOM1L2	GRCh38.p7	17:17905998	TGTCCCAGGACTTCT[C/G]GGTTTGCTGTTCCAT	146691
rs75191323	snp	A/C	0	0	intron-variant	TOM1L2	GRCh38.p7	17:17903615	GAGACTCCATCTCAA[A/C]AAAAAAAAAAAAAAA	146691
rs75239995	snp	A/G	0.0126979	0.078662	intron-variant, upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17971612	GACAAAGATGGAGAA[A/G]AAGGTGACATCCCAC	146691
rs75295960	snp	A/G	0.00874735	0.0655527	intron-variant	TOM1L2	GRCh38.p7	17:17949672	AGACAGCCATCCTGG[A/G]GAAGGAAGGACAGAA	146691
rs75406820	snp	A/T	0.0162398	0.0886349	intron-variant	TOM1L2	GRCh38.p7	17:17885300	AGGTTTCCTCAGATC[A/T]GAGACAACTAATGCT	146691
rs75411982	snp	C/T	0.0607341	0.163335	intron-variant	TOM1L2	GRCh38.p7	17:17901570	CCTTCAGCTTCAGGA[C/T]TACTCTCTGGAAAAG	146691
rs75438214	snp	A/G	0.0162398	0.0886349	intron-variant	TOM1L2	GRCh38.p7	17:17869593	TACATGCTTGTTCAT[A/G]AAACCAGACATGTGC	146691
rs75499446	snp	C/G	0.0275645	0.114116	intron-variant	TOM1L2	GRCh38.p7	17:17931159	CATTCAACCAAACCA[C/G]ACTCCTCTTTCCAAG	146691
rs75504959	snp	C/T	0.0391387	0.134304	intron-variant	TOM1L2	GRCh38.p7	17:17910416	GATGAATGACTGCAT[C/T]AGCAACCCTTCCTCT	146691
rs75561977	snp	C/T	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17912135	TCCACAAAACCGCCA[C/T]TGTCATCATGGCCGG	146691
rs75607932	snp	A/G	0.0130921	0.0798413	intron-variant	TOM1L2	GRCh38.p7	17:17880852	CCAGAGAGAGGAACT[A/G]TAATGTCATTCTTCC	146691
rs75620030	snp	A/G	0.0209421	0.100162	intron-variant	TOM1L2	GRCh38.p7	17:17876510	TAGTCTTGTTCTAGT[A/G]TCTAAGAAGACAGAC	146691
rs75657476	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17894062	AATTAGTTGGTAATT[G/T]AGGCACCAGTTTTGC	146691
rs75665393	snp	A/G	0.0263992	0.111815	intron-variant	TOM1L2	GRCh38.p7	17:17878773	ATTGAAAAGTGTGTG[A/G]GGCCTTGCAGTTCAC	146691
rs75728623	snp	C/G	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17891725	GGTAGGGGAGTGCAG[C/G]CCCAGAAGGAAGGGC	146691
rs75865442	snp	A/G	0.00597247	0.0543191	intron-variant	TOM1L2	GRCh38.p7	17:17894216	TCACAAGAGGAGGCT[A/G]CTATGACAGCTTGAA	146691
rs75924706	snp	C/G	0.029116	0.117091	intron-variant	TOM1L2	GRCh38.p7	17:17941812	AGATAACCTATGAAC[C/G]TCATTTTGCCTTAAA	146691
rs75942072	snp	C/G	0.0607341	0.163335	intron-variant	TOM1L2	GRCh38.p7	17:17893144	TGCTCTCTTTGATGC[C/G]TCTGGGCCTTTGCAC	146691
rs76027583	snp	A/C	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17948004	AGGAAAAGAAAATTA[A/C]TGAGTCAAGTGCTTT	146691
rs76044072	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17889467	GTGGAGCCCAACCTC[C/G]CCCTTCCCCTCAATC	146691
rs76059560	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17904938	CTTGCCAGTCCTGCC[A/G]GGTGAGCGTTCAAGG	146691
rs76075894	snp	C/T	0.0209421	0.100162	intron-variant	TOM1L2	GRCh38.p7	17:17914600	CCACTTTCCCCATCT[C/T]GTAGACAAGTATCAA	146691
rs76081513	snp	C/G	0.0391387	0.134304	intron-variant, downstream-variant-500B	TOM1L2, LOC100507131	GRCh38.p7	17:17858165	ATCAGGGTTGGGAGG[C/G]GGTCAACTTTTCAAA	146691
rs76099088	snp	G/T	0.0333695	0.124785	intron-variant	TOM1L2	GRCh38.p7	17:17903283	TTATTTAACAAATAT[G/T]TATTAACAGCTAATC	146691
rs76200634	snp	A/C	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17912131	CCATGATGACGATGG[A/C]GGTTTTGTCGAATAG	146691
rs76272425	snp	C/T	0.375	0.216506	intron-variant	TOM1L2	GRCh38.p7	17:17912401	AGACGGGGCGGCTGC[C/T]GGGCAGAGGGGCTCC	146691
rs76413864	snp	A/T	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17877891	TTAAAAAAAAAAAAA[A/T]ATCCCAAACCCCCTC	146691
rs76533378	snp	G/T	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17854266	TGAACCAAAGAAACT[G/T]TGGGAGGCCGAGGAC	146691
rs76595964	snp	A/G	0.0337553	0.125452	intron-variant	TOM1L2	GRCh38.p7	17:17934096	TCAAGACACAAACTA[A/G]TATATTTTTTATATT	146691
rs76612598	snp	C/T	0.00597247	0.0543191	intron-variant	TOM1L2	GRCh38.p7	17:17941805	AATCCACAGATAACC[C/T]ATGAACCTCATTTTG	146691
rs76696230	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17870569	AGTGAGTTAAGGGGA[A/T]AAGACATGAAGGATA	146691
rs76722346	snp	C/T	0.0640965	0.167152	intron-variant	TOM1L2	GRCh38.p7	17:17899112	GAGGGAGGTTTTTCA[C/T]TGGACTGCCTTTTTG	146691
rs76770797	snp	C/G	0.0618563	0.164627	intron-variant	TOM1L2	GRCh38.p7	17:17854088	TTAAGCTTATATAAC[C/G]TAAGCTTAAATTGAC	146691
rs76852760	snp	A/T	0.166506	0.235645	intron-variant	TOM1L2	GRCh38.p7	17:17868101	GGCTTAAATAGGTTT[A/T]ATAGGTTAAACCCAA	146691
rs76926781	snp	C/T	0.0150606	0.0854603	intron-variant	TOM1L2	GRCh38.p7	17:17901815	GCACATCAGAGTCAC[C/T]TGTAGTGCCATTCCC	146691
rs76962986	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17851213	AAGGTGGCTGTACGC[A/G]TTCTTGAAATGGAGA	146691
rs76970097	snp	C/T	0.021333	0.101051	intron-variant	TOM1L2	GRCh38.p7	17:17944947	CGGATGCTCCTGCAA[C/T]TCCCAACACCGTACT	146691
rs77026069	snp	C/T	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17954312	CATTTATAAATCATT[C/T]TTTTTTTTTTTTTTT	146691
rs77075870	snp	C/G	0.0372196	0.131242	intron-variant	TOM1L2	GRCh38.p7	17:17855657	GTCCCAGGAGCATAA[C/G]GGTTCCAACAGATGC	146691
rs77082949	snp	C/T	0.0607341	0.163335	intron-variant	TOM1L2	GRCh38.p7	17:17880542	GACCTTCCTTGCCCA[C/T]AGTGAAATATCATAG	146691
rs77151937	snp	A/G	0.00716266	0.059414	intron-variant	TOM1L2	GRCh38.p7	17:17903882	AGTGAAAGAGGTGAC[A/G]AGAACAGAAGGGACA	146691
rs77181590	snp	C/T	0.00676609	0.0577691	intron-variant	TOM1L2	GRCh38.p7	17:17850368	CCCTATCTCTGAGGA[C/T]GGAGACAATGGGTCT	146691
rs77257272	snp	A/G	0.021333	0.101051	intron-variant	TOM1L2	GRCh38.p7	17:17928581	CCCCAGACGGCCCCC[A/G]CGTGAGCATGCACAC	146691
rs77260701	snp	A/G	0.0126979	0.078662	intron-variant	TOM1L2	GRCh38.p7	17:17849652	GGGCCTCATTGGGAA[A/G]GGGCAGGATGGGGAA	146691
rs77293240	snp	A/G	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17855964	TATTTGTTGTAAAGA[A/G]AAAAAAAAAAACAAA	146691
rs77304058	snp	C/G	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17968149	CCCAGGACACCTTTT[C/G]TGAGCATGTTACCTC	146691
rs77310955	snp	A/G	0.0387552	0.1337	intron-variant	TOM1L2	GRCh38.p7	17:17911384	CATTAGCATATCACC[A/G]GAGAGGTCAGCACTT	146691
rs77322052	snp	A/G	0.0225045	0.103662	intron-variant	TOM1L2	GRCh38.p7	17:17940420	TAACTTGTCCAAAAA[A/G]TCATGCTGCCAATAT	146691
rs77334048	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17918415	CCATGTTGAATAGAA[A/G]TGGTGAAAGGCAGCA	146691
rs77356265	snp	G/T	0	0	intron-variant	TOM1L2	GRCh38.p7	17:17952674	TGCTGGGATTACAGG[G/T]GTGAGCCACCACACC	146691
rs77413472	snp	A/C	0.0142736	0.0832652	intron-variant	TOM1L2	GRCh38.p7	17:17949472	TACAGGATAAATACC[A/C]CCCCACTCCGATGCT	146691
rs77423543	snp	A/C	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17962960	AGTGAGACTCCGTCT[A/C]AAAAAAAAAAAAAAT	146691
rs77431985	snp	A/G	0.0193772	0.0965046	intron-variant	TOM1L2	GRCh38.p7	17:17851612	AAACACAGCAAAAAC[A/G]AGGGCTCTGATGACA	146691
rs77453338	snp	C/T	0.0607341	0.163335	intron-variant	TOM1L2	GRCh38.p7	17:17880440	AACAGAGACATCATA[C/T]ACTTTCTCCCCTTGC	146691
rs77502635	snp	C/T	0.0611083	0.163768	intron-variant	TOM1L2	GRCh38.p7	17:17904830	ACGGGACACATTTCT[C/T]CTGCCATCCTGGAAG	146691
rs77549844	snp	A/C	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17924299	GCTAATGGGTACGGA[A/C]TGATGAAAATGTTCT	146691
rs77574734	snp	A/G	0.16618	0.23553	intron-variant	TOM1L2	GRCh38.p7	17:17883666	GTGAACCCAGAAGGC[A/G]GAGCGTGCAGTGAGC	146691
rs77599969	snp	A/G	0.0209421	0.100162	intron-variant	TOM1L2	GRCh38.p7	17:17927069	CAAAGCTTGCCAAGG[A/G]AAACATGCAAATAAG	146691
rs77634794	snp	C/T	0.0368353	0.130617	intron-variant	TOM1L2	GRCh38.p7	17:17893371	CATGGTTCTTCCTAC[C/T]CCAAGTTTTCTCAGA	146691
rs77671185	snp	A/G	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17869322	GGAAAAAAAAAAAAA[A/G]AGAAATCCGGCTCCC	146691
rs77681052	snp	A/G	0.480461	0.0968913	intron-variant	TOM1L2	GRCh38.p7	17:17913033	CACCAAAAAAAATAC[A/G]AAAACCAGTCAGGCG	146691
rs77729440	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17916207	GCCTCCTGAGTAGCT[G/T]AGACTACAGGCGCCC	146691
rs77735858	snp	A/G	0.16911	0.236552	intron-variant	TOM1L2	GRCh38.p7	17:17962876	TGAGGCAGGAGAATC[A/G]CTTGAACCTGGGAGG	146691
rs77766992	snp	A/G	0.00636936	0.0560724	intron-variant	TOM1L2	GRCh38.p7	17:17940262	TTACTCAGATGAGAT[A/G]AGCTTATACGGGTCA	146691
rs77786709	snp	A/C	0	0	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17844487	ACTCACATGGAGGCG[A/C]TAATAGAAAGACAGG	146691
rs77788941	snp	C/T	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17912223	TCCTCACTTCCCAGA[C/T]GGGGCAGCCAGGCAG	146691
rs77818644	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17862872	ACAAAACAAATGGGT[C/G]GCAGATGAGAACAAA	146691
rs77821901	snp	A/G	0.0726307	0.176182	intron-variant	TOM1L2	GRCh38.p7	17:17896299	ATGCTTTATTTTGTG[A/G]GAAGCAGGTGGGAAA	146691
rs77840825	snp	C/T	0.00438332	0.0466095	intron-variant	TOM1L2	GRCh38.p7	17:17905297	CACATCTTCCAGGAG[C/T]CTGGCTGGCAGCAAA	146691
rs77890701	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17946248	CTACCCTCTTGAAGT[A/G]TACAATTCAGTGGCA	146691
rs77897450	snp	A/G	0.00737997	0.0602953	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17862352	ATCTCGCTGTAAGGA[A/G]TGGGTTCACCCTGCA	146691
rs77916160	snp	A/G			missense, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17882724	TCTGAATTGGCTGTG[A/G]TGGGGCCAGTCACAC	146691
rs77983901	snp	A/T	0.0275645	0.114116	intron-variant	TOM1L2	GRCh38.p7	17:17930007	GACCACTAGCAGAGA[A/T]ACAGAGCCCATGCCT	146691
rs77988845	snp	A/G	0.00438332	0.0466095	intron-variant	TOM1L2	GRCh38.p7	17:17915352	GGTACCACCAATTCA[A/G]TGATGGGATCCTGGC	146691
rs77995948	snp	C/T	0.0618563	0.164627	intron-variant	TOM1L2	GRCh38.p7	17:17911584	GTGAGGGAGCCCACA[C/T]TGAGTGGCCTTAGTT	146691
rs78000129	snp	G/T	0.0607341	0.163335	intron-variant	TOM1L2	GRCh38.p7	17:17873802	TGAGGAAGTTTTTCT[G/T]CAGAAGGCCACTGTC	146691
rs78021295	snp	C/T	0.0209421	0.100162	intron-variant	TOM1L2	GRCh38.p7	17:17941555	AGGGATTCCAAGCCA[C/T]GAGGAGATATCCACG	146691
rs78164263	snp	A/G	0.0240643	0.107019	intron-variant	TOM1L2	GRCh38.p7	17:17853377	CAACAAAGACATTAA[A/G]GGGTCAGGGGCCTTA	146691
rs78197992	in-del	-/AAA			intron-variant	TOM1L2	GRCh38.p7	17:17875282	AAGAAAAAAAAAAAA[-/AAA]GGACAGAAGGTGAGA	146691
rs78224599	snp	C/G	0.0391387	0.134304	intron-variant	TOM1L2	GRCh38.p7	17:17943211	AAGGCAGAAGCAGGT[C/G]TCAAACTGGGGTATG	146691
rs78228545	snp	A/G	0.0607341	0.163335	intron-variant	TOM1L2	GRCh38.p7	17:17908683	TAACAAGTATGTGAA[A/G]AGAGGTTCAACATCA	146691
rs78316700	snp	A/C/G			intron-variant	TOM1L2	GRCh38.p7	17:17962233	AAAATGGTAGTTGCC[A/C/G]GGGGCTGGGGGGAGG	146691
rs78435472	snp	A/C	0.0607341	0.163335	intron-variant	TOM1L2	GRCh38.p7	17:17894574	AGCCTCAGCATCCTC[A/C]TCTGTAAAGCAGAGA	146691
rs78447682	snp	C/T	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17912080	gacacagtaacaatc[C/T]gatttctctttcttt	146691
rs78514350	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17862873	CAAAACAAATGGGTG[G/T]CAGATGAGAACAAAA	146691
rs78639097	snp	C/T	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17911645	GATTAGCTGGAAATT[C/T]TTTTTTTTTTTTAAT	146691
rs78646914	snp	C/G/T	0.00953873	0.0683987	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847267	AGGCAGAGGTGAGCA[C/G/T]AGGGCGGGGCCGGGC	146691
rs78686345	snp	A/G	0.093417	0.194889	intron-variant	TOM1L2	GRCh38.p7	17:17925486	CAGCAAAAGACTAAG[A/G]AAGAAAGTGGCAAAC	146691
rs78692119	snp	A/C	0.106987	0.205054	intron-variant	TOM1L2	GRCh38.p7	17:17921260	TCCTCCCACTCCCCA[A/C]ACAAAGGAACCCTTC	146691
rs78759059	snp	A/G	0	0	intron-variant	TOM1L2	GRCh38.p7	17:17949800	CAGTGGGCAAGTTTA[A/G]GTGGGCCAGGGCAAT	146691
rs78804231	snp	A/C	0.00438332	0.0466095	intron-variant	TOM1L2	GRCh38.p7	17:17930444	AGACCCTCACGGTAG[A/C]CAGACACCTGGCAGG	146691
rs78819540	snp	A/T	0.5	0	intron-variant, downstream-variant-500B	TOM1L2, LOC100507131	GRCh38.p7	17:17858226	TTTTCTTTTTCCTAC[A/T]TTTTTTTTTTCTCTT	146691
rs78820309	snp	A/G	0.0607341	0.163335	intron-variant	TOM1L2	GRCh38.p7	17:17910249	CAGGAGCTCAGGATC[A/G]TCAGTGGCAGAGCCA	146691
rs78829178	snp	A/T	0.0236746	0.106192	intron-variant	TOM1L2	GRCh38.p7	17:17897503	TGTTACAGTTTCTAT[A/T]TTAAGAACTCACTGT	146691
rs78839717	snp	C/G	0.0618563	0.164627	intron-variant	TOM1L2	GRCh38.p7	17:17948962	AAGTATTGGGCAAAG[C/G]CAAAAAGTTAAGAGT	146691
rs78872339	snp	C/T	0.0209421	0.100162	intron-variant	TOM1L2	GRCh38.p7	17:17879170	ACAAGGGCTCCTGTG[C/T]ACAGTCAAGGTTGAA	146691
rs78921226	snp	A/C/G	0.0329836	0.124112	intron-variant	TOM1L2	GRCh38.p7	17:17919065	TTATAATGGAGTCTA[A/C/G]AACAGGGAGTGTGAA	146691
rs78943608	snp	A/T	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17962326	GTGATTGTTGCATAT[A/T]TTTTTTTTTTTAGGG	146691
rs79027773	snp	G/T	0.0618563	0.164627	intron-variant	TOM1L2	GRCh38.p7	17:17951761	GTGGTGCTTAGGAAG[G/T]AAGTTAGCCGAAGGC	146691
rs79055068	snp	C/T	0.0185938	0.0946107	intron-variant	TOM1L2	GRCh38.p7	17:17938021	TGGGATTTTGCCATA[C/T]GGTGGCTCTGCTTTG	146691
rs79165753	snp	G/T	0.00398564	0.0444627	intron-variant	TOM1L2	GRCh38.p7	17:17938663	AACCCAGCAGGCAGA[G/T]AGTCACAAACCAATA	146691
rs79236785	snp	A/G	0.0189856	0.0955633	intron-variant	TOM1L2	GRCh38.p7	17:17853089	CTGTGCTTGCTGGCA[A/G]GCCTTCTGCCTTGAG	146691
rs79315516	snp	A/G	0.0023933	0.0345097	intron-variant	TOM1L2	GRCh38.p7	17:17949259	AGCAGTGTGGAACTC[A/G]TGCCAGGAAAACCCA	146691
rs79333265	snp	G/T	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17917990	TATGAACACAGGATG[G/T]TTTTCCATATATTTA	146691
rs79380527	snp	C/T	0.0588605	0.161139	intron-variant	TOM1L2	GRCh38.p7	17:17941504	ATCATTACGCTGACT[C/T]CCATTAAGCCAGAAC	146691
rs79382853	snp	A/G	0.438105	0.164671	intron-variant	TOM1L2	GRCh38.p7	17:17875269	TCAAAAAGAAAAAAA[A/G]AAAAAAAAAAAAAAA	146691
rs79383804	snp	A/G	0.0614824	0.164198	intron-variant	TOM1L2	GRCh38.p7	17:17850168	CTACCCCATGACTCT[A/G]GGCAAGCCACTTCCC	146691
rs79396371	snp	A/G	0.0209421	0.100162	intron-variant	TOM1L2	GRCh38.p7	17:17937259	TGAATTCCCTCCTCC[A/G]GTTTTGTAACAAGCA	146691
rs79414011	snp	C/T	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17912163	CGGTTCTCAATGAGC[C/T]GCTGGGCACACCTCC	146691
rs79457691	snp	A/G	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17916209	CTCCTGAGTAGCTGA[A/G]ACTACAGGCGCCCAC	146691
rs79471489	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17870568	CAGTGAGTTAAGGGG[A/C]TAAGACATGAAGGAT	146691
rs79482298	snp	C/T	0.00676609	0.0577691	intron-variant	TOM1L2	GRCh38.p7	17:17950776	AGTAAAAAAAGTTAG[C/T]CAATACACAGAAAAT	146691
rs79512784	snp	C/T	0.0236746	0.106192	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17845466	TGGAATCCCTGCTCC[C/T]TTCAGAGCCTCCAGG	146691
rs79556089	snp	C/T	0.00510713	0.0502741	synonymous-codon, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17869402	CAGCTCCTCGGTGAC[C/T]TCCTCATTGGACACG	146691
rs79565780	snp	C/T	0.375	0.216506	intron-variant	TOM1L2	GRCh38.p7	17:17912314	CCCTCCCGGACGGGG[C/T]GGCTGCCGGGCGGAG	146691
rs79572919	snp	C/T	0.165853	0.235413	intron-variant	TOM1L2	GRCh38.p7	17:17882438	CTGTGTCAGGACCCT[C/T]TGCATGTCAGGTCCC	146691
rs79619630	snp	C/T	0.0189856	0.0955633	intron-variant	TOM1L2	GRCh38.p7	17:17883767	AATCCCTCATGCTTG[C/T]CCTTTGGGTATCTCA	146691
rs79649608	in-del	-/TT			intron-variant	TOM1L2	GRCh38.p7	17:17903848	ACTGAGAGATCCAGT[-/TT]GAATGACGGGATCTA	146691
rs79662763	snp	G/T	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17960204	TCATTCAGGCATTCA[G/T]TCACTCAATCCCACA	146691
rs79665189	snp	A/G	0.00953873	0.0683987	intron-variant	TOM1L2	GRCh38.p7	17:17896776	AAGACACAAGCAGAG[A/G]GCCCCTCAGGGCTTC	146691
rs79673844	snp	A/G	0.0150606	0.0854603	intron-variant	TOM1L2	GRCh38.p7	17:17936756	AATTGTACTTACAGC[A/G]TTATCTCTGTAAAGA	146691
rs79705505	snp	G/T	0.00358779	0.0422022	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17844236	CTGAGTTAGAGATGC[G/T]TGTCTGCGGGGGCCC	146691
rs79717717	snp	C/T	0.0209421	0.100162	intron-variant	TOM1L2	GRCh38.p7	17:17872418	GTTAACTTTGACAGA[C/T]CATCCTCCCCTGCTT	146691
rs79722366	snp	C/G	0.0618563	0.164627	intron-variant	TOM1L2	GRCh38.p7	17:17950693	TTTTATGTTACTTTA[C/G]ATTAATGCCAAGTGA	146691
rs79743842	snp	C/T	0.00636936	0.0560724	intron-variant	TOM1L2	GRCh38.p7	17:17853558	CCTCCTCAAAAATAA[C/T]TTCCCAAAAGCTGGC	146691
rs79817429	snp	A/C	0.00914312	0.0669923	intron-variant	TOM1L2	GRCh38.p7	17:17959492	CCTTTCAACTAGAGT[A/C]TTCTGATTCTTTGAA	146691
rs79834613	snp	C/T	0.0107246	0.0724382	intron-variant	TOM1L2	GRCh38.p7	17:17850280	GGCCAGCAGTTATCA[C/T]ATGCAGCCACTGCAG	146691
rs79886927	snp	A/G	0.0441095	0.141807	intron-variant	TOM1L2	GRCh38.p7	17:17848688	GGGACAAAGCCACCC[A/G]TGAAGCCCATGGCTC	146691
rs79905157	snp	A/T	0.0607341	0.163335	intron-variant	TOM1L2	GRCh38.p7	17:17908615	AAACTATCCAATTAA[A/T]AAATGGGAAAGGACT	146691
rs79953861	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17904937	CCTTGCCAGTCCTGC[A/C]AGGTGAGCGTTCAAG	146691
rs79996790	snp	A/G	0.00438332	0.0466095	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17845113	ACTCTGGGGCACCGG[A/G]GCTATACTTGCTTCC	146691
rs80070730	snp	C/T	0.0618563	0.164627	intron-variant	TOM1L2	GRCh38.p7	17:17946461	ATAAATGCAATCATA[C/T]AATATATAGCTGTTT	146691
rs80157839	snp	C/T	0.0618563	0.164627	intron-variant	TOM1L2	GRCh38.p7	17:17955935	CTGAAGTTGTTCGCT[C/T]CTACCGCCTGGAATT	146691
rs80185456	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17853779	CACCGGAGAGCTCCT[A/G]AGTTTCTTCTATCCT	146691
rs80236924	snp	A/G	0.0209421	0.100162	intron-variant	TOM1L2	GRCh38.p7	17:17968298	GTGTAAGCCCCATGC[A/G]GCTGTTGAGAAGTAT	146691
rs80337969	snp	C/T	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17911646	ATTAGCTGGAAATTC[C/T]TTTTTTTTTTTAATT	146691
rs80345000	snp	C/G	0.0111196	0.0737302	intron-variant	TOM1L2	GRCh38.p7	17:17855852	GCCTTTGATCTCACT[C/G]AATAGTACAAAAAGT	146691
rs80347931	snp	C/T	0.0107246	0.0724382	intron-variant	TOM1L2	GRCh38.p7	17:17926530	GAAAGGTCACGAATA[C/T]CAACAGTGAGAACAA	146691
rs111238555	snp	C/G	0.0217236	0.101931	intron-variant	TOM1L2	GRCh38.p7	17:17851968	TGACATGATAAGAAG[C/G]TCCCTAGAAGCCATG	146691
rs111240440	snp	A/C	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17875169	GGCTGAAGCAGGAGA[A/C]TCACTTGAACCCAGG	146691
rs111261278	in-del	-/A	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17903613	GCGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA	146691
rs111347018	snp	C/T	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17920057	GAAGACCCTGGCCTC[C/T]ACAATAGACGGTCCA	146691
rs111367557	snp	C/G	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17935572	TAGCTTAGAGGACTG[C/G]AGAAAGCAGAGGATG	146691
rs111367898	snp	G/T	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17953314	AAGGTAAATGTTATG[G/T]TATGTGTATTTTACC	146691
rs111386508	snp	A/C	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17949241	TGTTCTCCAATGGGG[A/C]ACAGCAGTGTGGAAC	146691
rs111427183	snp	A/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17950613	TTGGCGGGGAGCCTT[A/T]GGCAGACAACAGGAT	146691
rs111430123	snp	G/T	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17878455	CTGTGCCCCTAGGAC[G/T]GTGTTTTGTGTCAGG	146691
rs111430660	snp	C/T	0.0178098	0.0926698	intron-variant	TOM1L2	GRCh38.p7	17:17960619	CTAGTATTACAGGCA[C/T]GAGCCAGTGAGCCCA	146691
rs111432689	snp	A/C	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17907821	ATTAGGTTTATGAAC[A/C]CGTAGAGTCTGGAGC	146691
rs111513809	snp	A/G			intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17862406	GCTTCTCCTGTGGAT[A/G]AGGGGCCAGGCAGGG	146691
rs111530230	snp	G/T	0.0178098	0.0926698	intron-variant	TOM1L2	GRCh38.p7	17:17924039	GCTACTCGGGAGGCT[G/T]AGGCAGGAGAATTAC	146691
rs111535749	snp	A/G	0.0930568	0.194599	intron-variant	TOM1L2	GRCh38.p7	17:17885722	GAGGTCAGGAGATCA[A/G]GACCATCCTGGCTAA	146691
rs111563061	snp	A/C	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17966963	TCAGCTTTGGGACTC[A/C]GACTGGCTTCCTTGC	146691
rs111566634	snp	C/T	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17960790	AAAGAAAAGAATGCA[C/T]GTAAACTACATAACC	146691
rs111583066	snp	C/T	0.126909	0.217598	intron-variant	TOM1L2	GRCh38.p7	17:17952538	CTGGGACCACAGGTG[C/T]GTGCTGCCACCCCTG	146691
rs111583947	snp	C/T	1.65905e-05	0.0028801	intron-variant	TOM1L2	GRCh38.p7	17:17882886	GGCAACAACAAAGTC[C/T]TCTGTTTACCTGGGC	146691
rs111589513	snp	A/G	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17873174	TCAAGGCCTCAGGAT[A/G]TTTCCCCACTCCAGT	146691
rs111596308	snp	A/G/T	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17850699	TGGCCTCCGCAGGCC[A/G/T]GGAGGCCACTGCAGC	146691
rs111604873	snp	A/G	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17888944	AAGCTGAAAGCTGCC[A/G]GAAGGGAAGTCTTTG	146691
rs111629292	snp	C/T	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17934010	CCTAATCCACAGACA[C/T]ATTTAGATACTAGGT	146691
rs111642596	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17851153	GAGGAAAGCAATGAG[A/G]TGCAAATGATAAGAA	146691
rs111649260	snp	G/T	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17958260	GCCCCACCCAAAGTC[G/T]CACAGCAAATCAGCA	146691
rs111650396	snp	C/G	0.0123036	0.0774623	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17846558	GGTGGGAGGAGGCCA[C/G]ACTGTCAGGAGAGTC	146691
rs111653510	snp	G/T	0	0	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17844234	AACTGAGTTAGAGAT[G/T]CGTGTCTGCGGGGGC	146691
rs111679762	snp	A/C	0.5	0	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17859454	GCTTGGGATGGGACA[A/C]GGTAACCTGAAATGC	146691
rs111681206	snp	C/T	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17907157	TTGGGCTGCAGAGAC[C/T]AATGGCCACTGGGAA	146691
rs111788094	snp	C/T	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17879841	GTCTAGTGACAATCC[C/T]TCTCACTGGGAGATC	146691
rs111800464	snp	C/T	0.0232981	0.10548	intron-variant	TOM1L2	GRCh38.p7	17:17964167	CATATGTAACCAAGT[C/T]TGAGACTGGTTTTAA	146691
rs111809849	snp	A/T	0.0741063	0.177655	intron-variant	TOM1L2	GRCh38.p7	17:17874354	CAGCTCACTGCAACC[A/T]CCGCCTCCCAGGTTC	146691
rs111846807	snp	A/G	0.0894459	0.191631	intron-variant	TOM1L2	GRCh38.p7	17:17956843	GCCCGGTTCCCGCCC[A/G]CGCCTCTCCCTCCAC	146691
rs111860025	snp	C/G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17890720	AGGCAAGTGGTCATC[C/G/T]GGAAGGTGGGAGGTT	146691
rs111879805	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17857611	GAGATTATGCAAAAA[C/T]AGGAGGGGAAATTTG	146691
rs111882961	snp	C/G	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17866543	TGCTCTAGTACAGAA[C/G]CAAGGCCACTTCCCC	146691
rs111930624	snp	C/T	0.444444	0.157135	intron-variant	TOM1L2	GRCh38.p7	17:17869592	GTACATGCTTGTTCA[C/T]AAAACCAGACATGTG	146691
rs111973311	snp	A/G	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17915660	AGCTGGGACTTCAGG[A/G]ATGCACCACCACAAC	146691
rs111978994	snp	A/G	0.0225045	0.103662	intron-variant	TOM1L2	GRCh38.p7	17:17864655	TAGTTGGGATTACAG[A/G]CACACACCACCATGC	146691
rs112014667	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17918563	AGGAACCATAACAGG[A/T]TCTGCAGGTCTTTGC	146691
rs112029189	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17967640	GAGATGCAGTCTCGC[C/T]CTGTCATTCAGGCTG	146691
rs112067578	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17854877	GGGCAATGATCCAAG[C/T]TGAAGGCTGGTCTGA	146691
rs112086388	snp	C/G	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17875342	ACTTTTGCTACCACA[C/G]TGCCAGCCGGCCACC	146691
rs112123910	snp	C/T	0.444444	0.157135	intron-variant	TOM1L2	GRCh38.p7	17:17955027	AAAGCATTTATGGAA[C/T]TGAAATGATTGCATC	146691
rs112123927	snp	A/G	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17931194	CATCCCCACCTTTTC[A/G]TTACTACCTATTTTT	146691
rs112128938	snp	A/T	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17863207	CCAAGGACCTGGAAC[A/T]TCTATTTATTCAGCA	146691
rs112141002	snp	C/T	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17920078	AGACGGTCCAGAGTA[C/T]TGGATGCAGCCCACC	146691
rs112148928	snp	G/T	0.5	0	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17860861	TACCATTCCCTCCAC[G/T]TCACTGTGCCGCACC	146691
rs112236478	snp	C/T	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17940372	ATTAGAATCATTTTA[C/T]AGATGAGGAAGATGA	146691
rs112245587	snp	A/C	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17965813	AGGAATACAACATTA[A/C]ACTTTTTTTAAAACC	146691
rs112261227	snp	A/C	0.444444	0.157135	intron-variant	TOM1L2	GRCh38.p7	17:17969997	CAGAAGTATCAAGCT[A/C]TTTCCACTTGCTATA	146691
rs112262750	snp	C/T	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17954625	GCCCTATTTATAAAT[C/T]ATTCTAAAGGAGATG	146691
rs112307196	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17879534	CCACTGGACCTGTCC[C/T]GCCTTGCCGCTGTGT	146691
rs112367971	snp	C/T	0.105569	0.204058	intron-variant	TOM1L2	GRCh38.p7	17:17849536	TGGAGGCTCTGTGCA[C/T]TCAAAAATTAAAGTG	146691
rs112369842	snp	A/T	0.0023933	0.0345097	intron-variant	TOM1L2	GRCh38.p7	17:17890865	TTCAATTAAAAGTTT[A/T]AAAAAAAGAAAGGGC	146691
rs112370353	snp	A/G	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17892082	TTGAAGACCACAAAA[A/G]AGGATGATGTGAGAC	146691
rs112464513	snp	A/C	0.5	0	intron-variant, downstream-variant-500B	TOM1L2, LOC100507131	GRCh38.p7	17:17857996	ACCTCCACCCCAGCA[A/C]GTCCCCCTTACCTGC	146691
rs112479495	snp	C/T	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17897844	TCTTTTGGAGGGTGG[C/T]TGTAAACATATTCAT	146691
rs112490308	snp	C/T	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17921482	TTACGTGTGAGTCAG[C/T]GTGTGAGAGTAGCTG	146691
rs112501212	snp	C/G	0.0178098	0.0926698	intron-variant, upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17970846	GGCCCATAAGAACAC[C/G]AAAGATCCTGGCTCA	146691
rs112501627	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17943504	TGATCCAAAAGAGAA[C/T]GTAGGAATGTGAAGG	146691
rs112525639	snp	C/T	0.0123036	0.0774623	intron-variant	TOM1L2	GRCh38.p7	17:17910096	TTTTAAAAACCACCA[C/T]CAAAAAAGACAGAAA	146691
rs112528671	snp	C/T	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17919894	GTTCTCTCTCTCTAA[C/T]AGGAAGAAAATGAAG	146691
rs112532611	snp	C/T	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17887028	AGCAGCTAGAGTGCT[C/T]GGAGGTGCAGGCGTA	146691
rs112538429	snp	A/G			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847279	GCACAGGGCGGGGCC[A/G]GGCGTGCTCTTTCTC	146691
rs112547253	snp	A/G	0.093417	0.194889	intron-variant	TOM1L2	GRCh38.p7	17:17923864	AAAAAAAGGCCGGGC[A/G]CGGTGGCTGTCGCCT	146691
rs112550845	snp	C/T	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17880813	TCTACTACACACATA[C/T]GGCCCTTGTTCCTGC	146691
rs112567095	snp	C/T	0.126564	0.217402	intron-variant	TOM1L2	GRCh38.p7	17:17903403	CTGAGGCGGGCGGAT[C/T]ACGAGGTAAGGGGAT	146691
rs112567218	snp	C/G	0.0178098	0.0926698	intron-variant	TOM1L2	GRCh38.p7	17:17877743	TGATTTATAAGATAG[C/G]AGTGAGGGCTGGGAG	146691
rs112582045	snp	C/T	0.0178098	0.0926698	intron-variant	TOM1L2	GRCh38.p7	17:17889530	CAACCAAAGGGGCAG[C/T]GGGCTTTGGCCAGCA	146691
rs112610645	snp	A/C	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17873086	CACACTGCTTAAGGG[A/C]TCCTGAGAAGTTGGC	146691
rs112621342	snp	A/G	0.0463947	0.145069	intron-variant	TOM1L2	GRCh38.p7	17:17850692	GCACAGTTGGCCTCC[A/G]CAGGCCGGGAGGCCA	146691
rs112644943	snp	C/G	0.5	0	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17846973	GGGAGCCTGCAGGGA[C/G]CCTCGGTGCCAGGCT	146691
rs112665326	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17946673	GGTGCAGAGGCTGCA[A/G]GAGGCCTGTTTTGCT	146691
rs112682302	snp	A/G	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17853086	ACTCTGTGCTTGCTG[A/G]CAGGCCTTCTGCCTT	146691
rs112730117	snp	C/G	0	0	intron-variant	TOM1L2	GRCh38.p7	17:17945289	ACACACACACACACA[C/G]ACTCTCTCTCTCTCT	146691
rs112760381	snp	C/T	0.0376037	0.131863	intron-variant	TOM1L2	GRCh38.p7	17:17961728	AATACAAAAATTAGC[C/T]GGGCGTGGTGGCAGG	146691
rs112777834	snp	C/T	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17934950	TCATTACTCAGCCAC[C/T]GTGCTGCACTCAGCT	146691
rs112780317	snp	A/G	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17853144	GTTATCATGCTCTCA[A/G]TGACTGTAAGTCAGA	146691
rs112830338	snp	C/G	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17947052	AATTTTAACAGAAGT[C/G]CCTCAGGGTTAGGAA	146691
rs112909414	snp	A/G	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17949718	CTGGTGGTGTGTCCC[A/G]AAAAGGTGCACAGTC	146691
rs112922132	snp	C/G	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17952445	TCCCAGGCTGGAGTG[C/G]AGTGGTGTGATCTTA	146691
rs112956966	snp	A/C	0.093417	0.194889	intron-variant	TOM1L2	GRCh38.p7	17:17879405	TGGCATTTTATAATC[A/C]GGAAAAAAATGTTAT	146691
rs112960145	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17965174	GCTAAGGAGAAATCT[C/T]CCTACCTCTGTAATG	146691
rs112968102	in-del	-/T	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17970226	GCCTGGCTAATTTTC[-/T]TTTTTTTTTTTGGAT	146691
rs112983696	snp	C/T	0.0178098	0.0926698	intron-variant	TOM1L2	GRCh38.p7	17:17952282	ACTTCATGGAACATG[C/T]GCCACACACTAAGCA	146691
rs113010398	snp	C/T	0.0209421	0.100162	intron-variant	TOM1L2	GRCh38.p7	17:17892301	ACTTCCTGCATTCTC[C/T]GCTGCCTCTGCCTGG	146691
rs113046680	snp	C/T	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17917480	TTTTTTTTTTTTTTT[C/T]CAGAGACAGGGTCTT	146691
rs113061594	snp	A/C	0	0	intron-variant	TOM1L2	GRCh38.p7	17:17933860	TCAAATCCATCCTTC[A/C]AAAGATGATGATCTG	146691
rs113111319	snp	G/T	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17906392	CCTTGGCCTCCCAAG[G/T]TGCTAGGATTACAGA	146691
rs113119874	snp	A/C	0.444444	0.157135	intron-variant	TOM1L2	GRCh38.p7	17:17943333	TGCTGCTAATTAGAG[A/C]TAGGGAGTTAGGAAG	146691
rs113122975	snp	G/T	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17937695	CATGCTACAGTCTCT[G/T]TTCCTGCAGGCTGTA	146691
rs113143934	snp	A/G	0.0174175	0.0916809	intron-variant	TOM1L2	GRCh38.p7	17:17903499	GCGCCTGTAGTCCCA[A/G]CTACTCAGGAGGCTG	146691
rs113148998	snp	A/G	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17967399	TCTAGCCAACACAAG[A/G]AAAACTGCAAACTGC	146691
rs113168368	snp	A/G	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17908464	GAACTACATCAAAAT[A/G]AAAACTTCCAGGCAT	146691
rs113184106	snp	A/G	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17868226	CTGATGCACTGGGGG[A/G]TCCTGGGGATGCCCC	146691
rs113222208	snp	A/G	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17907379	ACCTGCCACCCTTAG[A/G]CCCTGACAAGCTTTG	146691
rs113241287	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17843617	GGATGCTCTGAGCCT[C/T]GGGTGCACTGACCCA	146691
rs113257509	snp	C/T	0.00755907	0.0610114	intron-variant	TOM1L2	GRCh38.p7	17:17917693	CCAGGCCAGCTCATG[C/T]CTGTAAATCCCATCA	146691
rs113278018	snp	A/G	0.126909	0.217598	intron-variant	TOM1L2	GRCh38.p7	17:17966053	TTAAACCCAGGAGGT[A/G]GAGGTTGCAGTGAGC	146691
rs113335514	snp	A/C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17951178	GATAATACCCACTCC[A/C/T]TTGCGGGGCTGCAAG	146691
rs113361397	snp	C/T	0.000184043	0.00959103	intron-variant, downstream-variant-500B	TOM1L2, LOC100507131	GRCh38.p7	17:17857881	AAAGTCACAGCAAGA[C/T]CCATGAGAAAGAAGT	146691
rs113440615	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17926525	ACATAGAAAGGTCAC[A/G]AATATCAACAGTGAG	146691
rs113446813	snp	C/T	0.5	0	downstream-variant-500B	TOM1L2	GRCh38.p7	17:17843088	ATTCAGTGCCCAGCA[C/T]AGGCTCTGCAGATGA	146691
rs113506356	snp	A/G	0.00716266	0.059414	intron-variant	TOM1L2	GRCh38.p7	17:17931573	CTCTCCCCCTCCCCC[A/G]TACAAAATGAGCTCC	146691
rs113541695	snp	C/T	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17850669	CTGTGCCCAAGGCCT[C/T]GCCCCCAGCACAGTT	146691
rs113588658	snp	C/T	0.0178098	0.0926698	intron-variant	TOM1L2	GRCh38.p7	17:17892018	ATGTCCCTGGGTTCT[C/T]AGGGAACGAAGAATG	146691
rs113592800	snp	C/T	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17915923	CTATTTTATGGTTGT[C/T]TTTTCACTCTCTTGA	146691
rs113605584	snp	C/T	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17880000	GAAAGCAGTACCACG[C/T]AGTGAAGGGCTCCGT	146691
rs113609739	snp	A/C	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17886534	GTGACGCCAACCTCA[A/C]AATGCCCTAGCATTT	146691
rs113663703	snp	A/G	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17903474	AAAAATTAGCTGGGC[A/G]TGGTGGCGGGCGCCT	146691
rs113678027	snp	C/T	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17889013	AACCAGGCTGCACCA[C/T]TCTCAATGTGTCTTT	146691
rs113693642	snp	A/G	0.5	0	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17862370	GGTTCACCCTGCATG[A/G]CTGCACCCTCCTGCT	146691
rs113718273	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17900331	TCAAGACCAGCCTGG[C/G]CAACATGGTGAAACC	146691
rs113763559	snp	A/G	0.0232847	0.105357	intron-variant	TOM1L2	GRCh38.p7	17:17956689	CAGCACTGGCGGGCC[A/G]GCACTGCTGGGGGAA	146691
rs113775891	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17910702	AGCCTCCCGAGTAGC[G/T]GGGATTACAGGCACG	146691
rs113799152	snp	A/G	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17943764	CTTCACTTCAGATAA[A/G]GTCTACACTCCTCAA	146691
rs113843062	snp	A/G	0.0221141	0.102801	intron-variant	TOM1L2	GRCh38.p7	17:17871055	AGTACTTCTGAGAGA[A/G]TTAATTAATGACTCT	146691
rs113843553	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17854330	GGCCCTGGTTGGAGC[A/G]GGGGGCACTGCGCTG	146691
rs113875432	snp	C/G	0	0	intron-variant	TOM1L2	GRCh38.p7	17:17955135	GATCTGATTTGCCCA[C/G]CTGACAAGTGAGAAG	146691
rs113876689	snp	A/G	0.0314385	0.121371	intron-variant	TOM1L2	GRCh38.p7	17:17969218	CCCACCACCACACCC[A/G]GCTCATTTTTGTATT	146691
rs113879084	in-del	-/AGGCATGGT	0.38928	0.208446	intron-variant	TOM1L2	GRCh38.p7	17:17917684	TTAGCTTCCCAGGCC[-/AGGCATGGT]AGCTCATGCCTGTAA	146691
rs113879421	snp	A/C	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17958192	CAACCTCTGTTCTTC[A/C]AAACAAACGAACGAA	146691
rs113881699	snp	C/T	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17899627	CTGTGGGCCTAGCAG[C/T]TGCCCCTGGCACAAA	146691
rs113893128	snp	C/T	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17913999	CCAGCTGGCCTCTCC[C/T]CTTCCTGGCTCAAAA	146691
rs113895896	snp	A/T	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17953855	CACAGTCCCCTGCAC[A/T]AGCAGGTGCTCTATG	146691
rs113897503	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17957634	CACAAAATATATATA[A/C]AGTATAACATATTTA	146691
rs113911262	snp	A/C	0	0	intron-variant	TOM1L2	GRCh38.p7	17:17884160	GATTGAATCCAGAAT[A/C]AATTCTGGATTGATG	146691
rs113942143	snp	G/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17966197	ACCTGAGGTCACCCC[G/T]CCCCTCCTACATTTC	146691
rs113947566	snp	A/T	0.5	0	intron-variant	TOM1L2	GRCh38.p7	17:17907636	CTTCTCCCAAGCAGA[A/T]GGGCTGAGCCAACAG	146691
rs113956376	snp	C/T	0.0178098	0.0926698	intron-variant	TOM1L2	GRCh38.p7	17:17958555	ACTACCCCATGCTTA[C/T]CCTCCCTGCCCATAT	146691
rs113971448	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17874334	GGAGTACGGTGGTAC[A/G]ATCTCAGCTCACTGC	146691
rs113975825	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17851425	CAGGTGCTCAGAGGG[C/G]AGGGCAGCACCAGCC	146691
rs114027168	snp	C/T	0.00914312	0.0669923	intron-variant	TOM1L2	GRCh38.p7	17:17870048	AACATTAATTAGTAA[C/T]AGTAAAAGGCCCTCC	146691
rs114053937	snp	C/T	0.0126979	0.078662	intron-variant	TOM1L2	GRCh38.p7	17:17856357	GGAACTGCCTTCTCA[C/T]GCAGAGCAGCAGTAT	146691
rs114061756	snp	C/G	0.0162398	0.0886349	intron-variant	TOM1L2	GRCh38.p7	17:17939044	TATAATGCAGCTACT[C/G]AGTAATGGGATGAAA	146691
rs114071057	snp	C/T	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17878599	AGCATGTGCCAGCAG[C/T]AGGGTAGAAGGTGTA	146691
rs114088267	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17863270	TAGATCTTGAGTAGA[A/C]CAAATTGAATCTGAT	146691
rs114092384	snp	A/C	0.0391387	0.134304	intron-variant	TOM1L2	GRCh38.p7	17:17923235	AAATCCTGGTCTCTA[A/C]TAAACATACAAAAAA	146691
rs114098732	snp	A/G	0.0168055	0.0901129	intron-variant	TOM1L2	GRCh38.p7	17:17933946	TGAGACCCTGCCTGA[A/G]ATGACAGTATTATCC	146691
rs114119595	snp	A/T	0.0614824	0.164198	intron-variant	TOM1L2	GRCh38.p7	17:17850419	CATCAAAAATCAGGA[A/T]GGGAGGAGGGGGATG	146691
rs114183672	snp	A/G	0.00755907	0.0610114	intron-variant	TOM1L2	GRCh38.p7	17:17855731	CCTGTCCAGTTTTCA[A/G]TGTAACAAGAACAAT	146691
rs114228354	snp	C/G	0.0170251	0.090679	intron-variant	TOM1L2	GRCh38.p7	17:17872715	GCTCCAGCGCTCCAG[C/G]TGTCTGCGGAAAATC	146691
rs114229625	snp	A/G	0.0168055	0.0901129	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847122	AAGCCAAATGTCACA[A/G]GGTGACAAGTCCAAG	146691
rs114269263	snp	A/T	0.0349115	0.127424	intron-variant	TOM1L2	GRCh38.p7	17:17947910	TGTTCTATTTTTTTT[A/T]AAATATATACTCTTT	146691
rs114347092	snp	A/G	0.0663309	0.169604	intron-variant	TOM1L2	GRCh38.p7	17:17909805	GAGGCTGAGGCAGGA[A/G]GGTTACTTGAATCCA	146691
rs114357186	snp	A/G	0.00636936	0.0560724	intron-variant	TOM1L2	GRCh38.p7	17:17862969	TGGGGAGGGTGGGGC[A/G]GGACTTTCCTTGGTA	146691
rs114397219	snp	C/T	0.00557542	0.0525036	intron-variant	TOM1L2	GRCh38.p7	17:17891706	GAATTCCTGGGGGTA[C/T]TGAGGTAGGGGAGTG	146691
rs114459022	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17961482	CAGGAGACTAAGGCA[A/G]GAGGATTGCTCGAGT	146691
rs114484048	snp	C/T	0.0387552	0.1337	intron-variant	TOM1L2	GRCh38.p7	17:17908876	CTATGGAAAACAGGA[C/T]GGTAGTTAAAACACA	146691
rs114493908	snp	A/G	0.0209421	0.100162	intron-variant	TOM1L2	GRCh38.p7	17:17960309	GCTCTGCCACTGATA[A/G]TCCACAGACCTTGAG	146691
rs114541585	snp	C/T	0.00438332	0.0466095	intron-variant	TOM1L2	GRCh38.p7	17:17924182	CTACATATTGTATGA[C/T]TCCATTTATATAAAA	146691
rs114549536	snp	A/G	0.0607341	0.163335	intron-variant	TOM1L2	GRCh38.p7	17:17929294	CTTCTGCTTAGAGCT[A/G]CTTTGAGCAGCAGGC	146691
rs114678748	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17908197	CTTTCTGACCACTCA[A/G]TGAGGAAAGGACAGT	146691
rs114720292	snp	A/T	0.0023933	0.0345097	intron-variant	TOM1L2	GRCh38.p7	17:17874762	TTCCCACTGGGGTGG[A/T]GGGTTAGACAGCTCC	146691
rs114738677	snp	C/T	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17902781	TAAAGTGAAATAGTA[C/T]ATCCACATAGATATA	146691
rs114741730	snp	A/C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17949309	ACTGAACATCTAGCA[A/C/T]GGCAGAGCATAGAGC	146691
rs114749091	snp	A/G	0.0162398	0.0886349	intron-variant	TOM1L2	GRCh38.p7	17:17880334	CACCCAGCTCCCTAC[A/G]TGGTAACACAGCCCC	146691
rs114777135	snp	A/C	0.0391387	0.134304	intron-variant	TOM1L2	GRCh38.p7	17:17855072	AGTGGTTAGACCAGC[A/C]CTGCCCATTTTCAAA	146691
rs114781342	snp	A/G	0.0391387	0.134304	intron-variant	TOM1L2	GRCh38.p7	17:17910213	GGAAACCCGGGGCCC[A/G]CAGAAGAAAAGGGAA	146691
rs114787101	snp	A/G	0.00755907	0.0610114	intron-variant	TOM1L2	GRCh38.p7	17:17869808	CAGACACCGTTCTCC[A/G]TCACTTGGTACAGAC	146691
rs114873147	snp	A/G	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17876872	TGTCACTGGGGACAC[A/G]CAGAAAGACCCAACA	146691
rs114874245	snp	C/T	0.0209421	0.100162	intron-variant	TOM1L2	GRCh38.p7	17:17931457	GTCTCTGAGCCTCAG[C/T]TTCCACATCTATAGA	146691
rs114887754	snp	C/T	0.0209421	0.100162	intron-variant	TOM1L2	GRCh38.p7	17:17904204	TCACTGAGGTGCTCT[C/T]ACTCAAAAAGGTAGC	146691
rs114923482	snp	A/G	0.00597247	0.0543191	intron-variant	TOM1L2	GRCh38.p7	17:17854188	TTATAACAGGGCAAA[A/G]TTCCTTCTAATAATG	146691
rs114926222	snp	C/T	0.0618563	0.164627	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17844233	CAACTGAGTTAGAGA[C/T]GCGTGTCTGCGGGGG	146691
rs115046828	snp	C/G	0.0209421	0.100162	intron-variant	TOM1L2	GRCh38.p7	17:17870096	TTACTTACACTTCCA[C/G]CAACAGCAGGAGTGT	146691
rs115071927	snp	A/C	0.00636936	0.0560724	intron-variant	TOM1L2	GRCh38.p7	17:17946383	CATTCCCCCTCTCCC[A/C]GCCTCCTACAACCAC	146691
rs115112944	snp	C/T	0.0170251	0.090679	intron-variant	TOM1L2	GRCh38.p7	17:17863275	CTTGAGTAGACCAAA[C/T]TGAATCTGATATGGT	146691
rs115119456	snp	C/T	0.0130921	0.0798413	intron-variant	TOM1L2	GRCh38.p7	17:17945901	TTTGAGACAAGGTCT[C/T]AGTGTCACCCAGGCT	146691
rs115137474	snp	A/G	0.0166325	0.0896639	intron-variant	TOM1L2	GRCh38.p7	17:17956802	GCCCACCCAGAACTC[A/G]CGCTGGCCCGCAAGC	146691
rs115170028	snp	C/T	0.00716266	0.059414	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17860877	TCACTGTGCCGCACC[C/T]CCTCACCGCCACAGG	146691
rs115174410	snp	A/C	0.00795532	0.062565	intron-variant	TOM1L2	GRCh38.p7	17:17894311	ACCCTGCTTCTGCAA[A/C]CAAAATTGGCAATGA	146691
rs115175666	snp	C/T	0.00478085	0.0486577	intron-variant	TOM1L2	GRCh38.p7	17:17942343	AGACCTGGGCTCAAA[C/T]TCCTGGCTCTGTAAT	146691
rs115181587	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17939787	ATAAATGTAATGAAA[A/G]TATAAGTAAGGGAAA	146691
rs115189547	snp	A/G	0.00874735	0.0655527	intron-variant	TOM1L2	GRCh38.p7	17:17940580	GAGCTGTGACTCCTG[A/G]ACAAAGAGCAGGAAT	146691
rs115223465	snp	C/G	0.0633504	0.166319	intron-variant	TOM1L2	GRCh38.p7	17:17960222	ACTCAATCCCACAAA[C/G]AATACTAAGCTCTCT	146691
rs115229075	snp	A/G	0.021333	0.101051	intron-variant	TOM1L2	GRCh38.p7	17:17895461	ACACTGACTGAATGC[A/G]ACTATATGCCAGGCA	146691
rs115234022	snp	C/T	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17903311	ATCAAATGCATTGTG[C/T]TAGGTGCTAGGGACA	146691
rs115247602	snp	C/T	0.0240643	0.107019	intron-variant	TOM1L2	GRCh38.p7	17:17937216	ATGAACCCTTCCTCC[C/T]ACAGAAGTGATGATC	146691
rs115304353	snp	A/T	0.0150606	0.0854603	intron-variant	TOM1L2	GRCh38.p7	17:17961113	AATTAAAAACTAGGC[A/T]CAGGACTTGAACAGA	146691
rs115345706	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17851978	AGAAGCTCCCTAGAA[A/G]CCATGTTAATGGAAT	146691
rs115349495	snp	C/T	0.0209421	0.100162	intron-variant	TOM1L2	GRCh38.p7	17:17908563	TTAATATCCAGACTA[C/T]GTAAAGAACTCCTAT	146691
rs115401934	snp	C/T	0.0193772	0.0965046	intron-variant	TOM1L2	GRCh38.p7	17:17880879	TTCCTGCACTGTGAC[C/T]CAGCTTAAGTGACAA	146691
rs115406681	snp	A/G	0.00914312	0.0669923	intron-variant	TOM1L2	GRCh38.p7	17:17854434	CATCTGTCAGACTAG[A/G]GGCTGGCCCAGCAGA	146691
rs115454933	snp	C/T	0.0618563	0.164627	intron-variant	TOM1L2	GRCh38.p7	17:17849172	CTGGGCTGCAGAGGG[C/T]GGGACCCCACCTTTG	146691
rs115459657	snp	A/G	0.0209421	0.100162	intron-variant	TOM1L2	GRCh38.p7	17:17940907	AGCAATGAGGTGATT[A/G]GTTTTGCATTCCTAC	146691
rs115526241	snp	A/G	0.0193772	0.0965046	intron-variant	TOM1L2	GRCh38.p7	17:17937462	AGGTAAGAATGGTGA[A/G]GGCCAAAGATCTGTA	146691
rs115553254	snp	G/T	0.00914312	0.0669923	intron-variant	TOM1L2	GRCh38.p7	17:17855108	CAGACATCTTGGATG[G/T]CAGAAGCCACAGGTT	146691
rs115597364	snp	C/T	0.0209421	0.100162	intron-variant	TOM1L2	GRCh38.p7	17:17863159	CCATAATGCCCTTCT[C/T]GCTTGGGCTCCTCAT	146691
rs115603986	snp	A/T	0.0345262	0.126772	intron-variant	TOM1L2	GRCh38.p7	17:17876483	AAGGATCTACCCATG[A/T]GAAAGAGGAATTAGT	146691
rs115624824	snp	C/T	0.00636936	0.0560724	intron-variant	TOM1L2	GRCh38.p7	17:17969651	TGGTGAATCCTGGGG[C/T]CTGGTAGGGTATTTT	146691
rs115717097	snp	C/T	0.00874735	0.0655527	intron-variant	TOM1L2	GRCh38.p7	17:17870552	GGGCACTGGAGGGTG[C/T]CAGTGAGTTAAGGGG	146691
rs115722989	snp	A/G	0.0349115	0.127424	intron-variant	TOM1L2	GRCh38.p7	17:17927153	AGAAAAATAAACACA[A/G]TATCTATCTAGTTTC	146691
rs115747322	snp	A/G	0.0322114	0.122752	intron-variant	TOM1L2	GRCh38.p7	17:17869861	TTCATAATGTATCTC[A/G]CCATTCTTCTATTGC	146691
rs115756671	snp	A/G	0.0618563	0.164627	intron-variant	TOM1L2	GRCh38.p7	17:17949175	AATATATTTATTCTT[A/G]CCACCTGCCATTAAG	146691
rs115790948	snp	G/T	0.0119091	0.0762411	intron-variant	TOM1L2	GRCh38.p7	17:17940662	TGCCATTCCGATGAA[G/T]TTCAAGGCAAATTCT	146691
rs115791750	snp	C/G/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17880346	TACATGGTAACACAG[C/G/T]CCCTTGAAAAATACC	146691
rs115796741	snp	A/T	0.00636936	0.0560724	intron-variant	TOM1L2	GRCh38.p7	17:17966540	AACCTACTGAAACAG[A/T]AACTCTGAGGGTAGG	146691
rs115901542	snp	C/T	0.00517822	0.0506191	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17843890	CCTATGGCTGGTGGC[C/T]GCAGGGGAAGCCTGA	146691
rs115938796	snp	A/G	0.0182019	0.0936463	intron-variant	TOM1L2	GRCh38.p7	17:17946026	GGGGTGCACCATCAC[A/G]CCTGCCTGGCTAAAT	146691
rs115940195	snp	C/T	0.0607341	0.163335	intron-variant	TOM1L2	GRCh38.p7	17:17909621	GGGAATGGGGAGTTA[C/T]TGTTTAATGAACACA	146691
rs115973167	snp	A/T	0.00636936	0.0560724	intron-variant	TOM1L2	GRCh38.p7	17:17924517	ATTATTTAAAATCCT[A/T]AGCTGGGTGCAGTGG	146691
rs116001567	snp	A/T	0.104149	0.203046	intron-variant	TOM1L2	GRCh38.p7	17:17854533	TTTATTTAATTAATT[A/T]ATTTATTTAGAGACA	146691
rs116127128	snp	C/T	0.0209421	0.100162	intron-variant	TOM1L2	GRCh38.p7	17:17904850	CATCCTGGAAGACAG[C/T]CCCTCCAGGAAGCAT	146691
rs116142630	snp	C/T	0.0111196	0.0737302	intron-variant	TOM1L2	GRCh38.p7	17:17857362	TTCACAGGCACTGGG[C/T]TACAGAGGGCTTCCC	146691
rs116151361	snp	C/T	0.00438332	0.0466095	intron-variant	TOM1L2	GRCh38.p7	17:17964946	CAGGGGTTTTAAGAC[C/T]TGTCCAGGCAATTAA	146691
rs116174842	snp	A/G	0.00438332	0.0466095	intron-variant	TOM1L2	GRCh38.p7	17:17944034	GCTGCTACATTATCA[A/G]AGCACCCCCACACTG	146691
rs116217143	snp	A/G	0.021333	0.101051	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17846306	GGGCCCAAGACACAC[A/G]GGGATGCATACAGCT	146691
rs116233213	snp	C/T	0.00438332	0.0466095	intron-variant	TOM1L2	GRCh38.p7	17:17864819	ATTTTAAGTATTAAA[C/T]CTGGCAGTCATATAT	146691
rs116235575	snp	A/T	0.0134861	0.0810011	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17859071	CACGATTTTCTCCCA[A/T]TCATTTTATTTTATT	146691
rs116238840	snp	C/G	0.0166325	0.0896639	intron-variant	TOM1L2	GRCh38.p7	17:17961081	AGAACTCCTAAAACC[C/G]AACAACAACAAAACC	146691
rs116239767	snp	A/T	0.0162398	0.0886349	intron-variant	TOM1L2	GRCh38.p7	17:17917799	ATCCCTACAAAAAAT[A/T]TAAAAATTAGCCAGG	146691
rs116262834	snp	C/T	0.0158469	0.0875917	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17843937	AGGAAGGGCTGGTGA[C/T]GGGCACTGGGGGAGG	146691
rs116285429	snp	A/C	0.00953873	0.0683987	intron-variant	TOM1L2	GRCh38.p7	17:17968740	CTGTGCCCAAACCCT[A/C]CTTGCCACCACTCCC	146691
rs116297752	snp	C/G	0.0178098	0.0926698	intron-variant	TOM1L2	GRCh38.p7	17:17943613	GGGATTGCTGCTGCA[C/G]CCTCCTCATTGTTAT	146691
rs116343777	snp	A/G	0.00795532	0.062565	intron-variant	TOM1L2	GRCh38.p7	17:17883782	CCCTTTGGGTATCTC[A/G]GATGACCTCTTGCAC	146691
rs116345190	snp	C/T	0.0130921	0.0798413	intron-variant	TOM1L2	GRCh38.p7	17:17894776	CGTCTACTACAAATA[C/T]AAAAACTAGCCAGGC	146691
rs116376954	snp	C/T	0.00478085	0.0486577	intron-variant	TOM1L2	GRCh38.p7	17:17964162	AATAACATATGTAAC[C/T]AAGTCTGAGACTGGT	146691
rs116435662	snp	G/T	0.00636936	0.0560724	intron-variant	TOM1L2	GRCh38.p7	17:17915533	TTTTTTAAGAGACAG[G/T]ATCTCACTTTGTCAC	146691
rs116437711	snp	A/G	0.0209421	0.100162	intron-variant	TOM1L2	GRCh38.p7	17:17897810	TTTCATCATCTGTAC[A/G]GGGGAGGATAGTAAA	146691
rs116438132	snp	C/T	0.00676609	0.0577691	intron-variant	TOM1L2	GRCh38.p7	17:17931921	TAATATAACCCGAGG[C/T]GGCCACCTTACCCAA	146691
rs116559410	snp	C/G	0.0162398	0.0886349	intron-variant	TOM1L2	GRCh38.p7	17:17873919	AATTTTATTTGTGGA[C/G]GAAAAGGTTCCATAC	146691
rs116560884	snp	A/G	0.00557542	0.0525036	intron-variant	TOM1L2	GRCh38.p7	17:17881683	TACTGATGGGAGACC[A/G]GGGTTAAATGTCCTG	146691
rs116610797	snp	G/T	0.00636936	0.0560724	intron-variant	TOM1L2	GRCh38.p7	17:17930679	ACTTCCAAAAGGAAT[G/T]TAGGGTAATTTTAGT	146691
rs116637581	snp	A/G	0.0126979	0.078662	intron-variant	TOM1L2	GRCh38.p7	17:17910487	TGGGGAGCTTCTAGA[A/G]AGCACCAATACCTGA	146691
rs116652573	snp	C/T	0.0166325	0.0896639	intron-variant	TOM1L2	GRCh38.p7	17:17877044	TTCCTTCTCCTCAGG[C/T]GCTCCAGCTACGCTG	146691
rs116667542	snp	A/G	0.00636936	0.0560724	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17846631	GCCTTAGTGCTGCCC[A/G]GGCCTCTCAGTCACT	146691
rs116670186	snp	A/G	0.0209421	0.100162	intron-variant	TOM1L2	GRCh38.p7	17:17908873	CTGCTATGGAAAACA[A/G]GACGGTAGTTAAAAC	146691
rs116687148	snp	A/G	0.0607341	0.163335	intron-variant	TOM1L2	GRCh38.p7	17:17924173	TAAAAATGACTACAT[A/G]TTGTATGATTCCATT	146691
rs116701289	snp	A/C/G	0.00636936	0.0560724	intron-variant, upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17971084	TCTCTGGTGTCCCCA[A/C/G]GTGTCCACATCCCCC	146691
rs116711019	snp	C/T	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17892561	CATGCCTCCTCAGCA[C/T]GCATGGCCACTGGCC	146691
rs116746344	snp	A/G	0.00636936	0.0560724	intron-variant	TOM1L2	GRCh38.p7	17:17935781	TGATGAAATACAGTT[A/G]GCAAATCAACCTAAA	146691
rs116765277	snp	A/G	0.00438332	0.0466095	intron-variant	TOM1L2	GRCh38.p7	17:17953870	AAGCAGGTGCTCTAT[A/G]CATGTTCATTGCCTT	146691
rs116778100	snp	A/C	0.0240643	0.107019	intron-variant	TOM1L2	GRCh38.p7	17:17918558	AAAACAGGAACCATA[A/C]CAGGATCTGCAGGTC	146691
rs116845981	snp	C/T	0.00676609	0.0577691	intron-variant	TOM1L2	GRCh38.p7	17:17954904	TAAGGCCAAGAGAGG[C/T]CCCAGAACCTCCATG	146691
rs116859428	snp	C/G	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17945166	AGCTTTCTTTTCAGA[C/G]ATGATTTTATGCAGT	146691
rs116891426	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17861691	CCTGAAACCTTGACA[C/T]TGAGCAGAGGCTAAG	146691
rs116954588	snp	C/G	0.00676609	0.0577691	intron-variant	TOM1L2	GRCh38.p7	17:17864787	AAAGTCTTGGGATTA[C/G]CGGTGTTACACTTTG	146691
rs116982623	snp	C/T	0.0329836	0.124112	intron-variant	TOM1L2	GRCh38.p7	17:17937141	AAGGAGAGCAATGCC[C/T]GGCAAATTGTCCCTA	146691
rs116986961	snp	A/G	0.00192803	0.0309887	intron-variant	TOM1L2	GRCh38.p7	17:17869331	AAAAAAAAGAAATCC[A/G]GCTCCCACCTCTCGT	146691
rs117049692	snp	C/T	0.115788	0.21092	upstream-variant-2KB, utr-variant-5-prime, intron-variant	TOM1L2, DRC3	GRCh38.p7	17:17973725	GCAGTCCTTCCACCT[C/T]GGCCTCCCAAAGAGC	146691
rs117075284	snp	A/G	0.0232847	0.105357	intron-variant	TOM1L2	GRCh38.p7	17:17901865	TGATTGTGTAGGTCT[A/G]AGGTGAGGCCTGGAA	146691
rs117279893	snp	A/T	0.00636936	0.0560724	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17859422	CTTGGCCTCGTTTTC[A/T]TTTCGAGGTCAGCAT	146691
rs117296440	snp	C/G	0.00478085	0.0486577	intron-variant	TOM1L2	GRCh38.p7	17:17848076	TTCCAGATCAGCACT[C/G]GGGGTGGGGCAGGGT	146691
rs117327272	snp	C/T	0.0162398	0.0886349	intron-variant	TOM1L2	GRCh38.p7	17:17885288	AAGGCTAACTACAGG[C/T]TTCCTCAGATCAGAG	146691
rs117337033	snp	C/G/T	0.00517822	0.0506191	intron-variant	TOM1L2	GRCh38.p7	17:17915046	CTATCTAGTTTGTTA[C/G/T]GTAAAAAACAAGTGT	146691
rs117368055	snp	C/T	0.0182019	0.0936463	intron-variant	TOM1L2	GRCh38.p7	17:17956817	GCGCTGGCCCGCAAG[C/T]GCCACGCGCAGCCCG	146691
rs117416477	snp	A/G	0.0329836	0.124112	intron-variant	TOM1L2	GRCh38.p7	17:17926471	AAAGCCAAATACAAT[A/G]GGGTTCTAGATCATC	146691
rs117419095	snp	C/T	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17862316	GAGCCTCTGCTCTGA[C/T]CACTTATTTTAGTCA	146691
rs117422442	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17930694	TTAGGGTAATTTTAG[C/T]AATAATTTATACCCA	146691
rs117426903	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17948048	AATTTGAACATTAAA[C/T]AATTCTAAGAGATAT	146691
rs117544762	snp	C/T	0.00358779	0.0422022	intron-variant	TOM1L2	GRCh38.p7	17:17953022	GCCCAACAGACTGGT[C/T]CCCACCCCTTCATTT	146691
rs117561333	snp	A/G	0.0189856	0.0955633	intron-variant	TOM1L2	GRCh38.p7	17:17883419	GTCTGGAGGGATCAT[A/G]ATGAAAACAGCCTCC	146691
rs117601338	snp	A/G	0.0329836	0.124112	intron-variant	TOM1L2	GRCh38.p7	17:17937133	AAAGGATAAAGGAGA[A/G]CAATGCCTGGCAAAT	146691
rs117603004	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17884354	AGCAGGTGCTAATGA[A/C]CCTCACAGGATGGCT	146691
rs117688336	snp	C/T	0.0111196	0.0737302	intron-variant	TOM1L2	GRCh38.p7	17:17956822	GGCCCGCAAGCGCCA[C/T]GCGCAGCCCGGTTCC	146691
rs117696856	snp	A/G	0.0189856	0.0955633	intron-variant	TOM1L2	GRCh38.p7	17:17956684	CAGCACAGCACTGGC[A/G]GGCCGGCACTGCTGG	146691
rs117718998	snp	A/G	0.0193772	0.0965046	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17858892	GGCCCTAATTTTTGC[A/G]TTTTTATTAGAGACA	146691
rs117795168	snp	A/C/T	0.0162398	0.0886349	intron-variant	TOM1L2	GRCh38.p7	17:17853254	GAAAATAGTCCCACA[A/C/T]TAGCGGTTAGAGTGT	146691
rs117815291	snp	C/T	0.0364509	0.129988	intron-variant	TOM1L2	GRCh38.p7	17:17960526	ATTTTTTTGTAGAGA[C/T]GGAATTTCGCCATGT	146691
rs117850964	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17887815	CCGAGTCTCTCACCC[A/G]TGTACAGAGAAGGCA	146691
rs117861021	snp	C/T	0.0170251	0.090679	intron-variant	TOM1L2	GRCh38.p7	17:17911103	AGGTTTCAGAGAACA[C/T]AGGAGGGTGGGTGGG	146691
rs117890270	snp	A/G	0.0337553	0.125452	intron-variant	TOM1L2	GRCh38.p7	17:17967464	CATGTATGTCATCCA[A/G]CTCCAAGCAGTTGTG	146691
rs117898889	snp	A/G	0.00676609	0.0577691	intron-variant	TOM1L2	GRCh38.p7	17:17930371	GGTTAAAAAAAAGGG[A/G]GGTCTGGGAATGTGT	146691
rs117915049	snp	C/G	0.00597247	0.0543191	intron-variant	TOM1L2	GRCh38.p7	17:17899775	TACTGGTCTTTCCCA[C/G]CTTGCACGTTTGTTA	146691
rs117924262	snp	C/G	0.0193772	0.0965046	intron-variant	TOM1L2	GRCh38.p7	17:17854206	CCTTCTAATAATGTA[C/G]GTGCTATCAGACTCA	146691
rs117924544	snp	C/T	0.245631	0.249962	intron-variant	TOM1L2	GRCh38.p7	17:17956786	GGCCCGCTGAGCTCA[C/T]GCCCACCCAGAACTC	146691
rs117929409	snp	A/C/G	3.30591e-05	0.00406554	synonymous-codon, upstream-variant-2KB, intron-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17861524	AGAAGCAAGTCCTCC[A/C/G]ACAGCCTGAGGATCC	146691
rs117929831	snp	C/T	0.0325976	0.123435	intron-variant	TOM1L2	GRCh38.p7	17:17957066	TCGCTGCAGTCTCCA[C/T]CTCCTGGGCTCAAGC	146691
rs117960192	snp	C/T	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17964782	AAATAAAAAGCACAA[C/T]TATATGAGAATTTTA	146691
rs117964680	snp	C/T	0.0329836	0.124112	intron-variant	TOM1L2	GRCh38.p7	17:17863642	TTAGCCTTGACCTCC[C/T]GGGCTAAGTGATCCT	146691
rs118016722	snp	A/C			intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17860882	GTGCCGCACCCCCTC[A/C]CCGCCACAGGACACC	146691
rs118022455	snp	C/T	0.0165278	0.0893908	intron-variant	TOM1L2	GRCh38.p7	17:17925025	GCACTCCCTCCTCCA[C/T]TCTCTCTCTCTGTTT	146691
rs118075439	snp	C/T	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17895460	AACACTGACTGAATG[C/T]GACTATATGCCAGGC	146691
rs118100410	snp	C/T	0.00636936	0.0560724	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17859426	GCCTCGTTTTCATTT[C/T]GAGGTCAGCATGGCT	146691
rs118143947	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17868052	TTGGGTGAAAATACT[C/T]ATATTAGTTAGCTCC	146691
rs118157950	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17909991	ATATGATTGAGCCAC[C/T]GCATTCCAGCCTAGG	146691
rs118161505	snp	C/T	0.00835141	0.0640778	intron-variant	TOM1L2	GRCh38.p7	17:17907867	CAAATACAGGCTCCA[C/T]TACTTACTAGTTGTG	146691
rs118179422	snp	A/G	0.0379877	0.132479	intron-variant	TOM1L2	GRCh38.p7	17:17874983	AAGAAAAGGCCATGC[A/G]TGGTGGCTCACACCT	146691
rs118190519	snp	C/G	0.0325976	0.123435	intron-variant	TOM1L2	GRCh38.p7	17:17944507	TGATCCGTGGGATCA[C/G]AGATTTGGTGTCTTA	146691
rs137857564	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17931780	GCCAAACTTTACACA[C/T]GTGACACTGTTAGCC	146691
rs137864824	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847507	CCTGGGAGCAGACAC[A/G]GTGGCATTTCCATGG	146691
rs137936959	snp	C/G	0.00557542	0.0525036	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17860948	ACAAACCCTGGCTCT[C/G]GAGTGCCTTCTAATG	146691
rs137956304	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17894537	CACTTTCTCCCTGAA[C/T]GGCCCAGGACAGATC	146691
rs137959916	snp	A/G	0.0524604	0.153226	intron-variant	TOM1L2	GRCh38.p7	17:17946764	GAGTCTCACTCTATC[A/G]CCCAGGCTGGAGCGC	146691
rs137981880	snp	C/T	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17893367	CTAACATGGTTCTTC[C/T]TACTCCAAGTTTTCT	146691
rs137990788	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17910661	TGCAACCTTTACCTC[C/T]TGGGTTCAAGCAATT	146691
rs138010646	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17926489	GTTCTAGATCATCTG[A/G]GAAATTACTCCTATT	146691
rs138033123	snp	C/G	0.000399281	0.0141238	intron-variant, splice-acceptor-variant, downstream-variant-500B	TOM1L2, LOC100507131	GRCh38.p7	17:17857856	CGAGGACAGAAAAGT[C/G]TCAGAAAGAAAAGTC	146691
rs138054008	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17889413	TGAGCTCTATCACCC[A/G]CTTCCCTATAGGCAC	146691
rs138118323	snp	A/C	0.0023933	0.0345097	intron-variant	TOM1L2	GRCh38.p7	17:17965052	CTTCATAGACAGTGT[A/C]CCTACCCTTGACCAC	146691
rs138120331	snp	A/C	0.00795532	0.062565	intron-variant	TOM1L2	GRCh38.p7	17:17877913	AACCCCCTCTCCCCC[A/C]AAAACACGAAGTATT	146691
rs138140910	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17937553	GTCACCAGTGGGGGA[A/G]GGCCTTTCCCAGTGA	146691
rs138142115	snp	A/G	0.0023933	0.0345097	intron-variant	TOM1L2	GRCh38.p7	17:17884531	TAAGAAAGCATGATG[A/G]CAAGCTGAATAATTC	146691
rs138147144	snp	A/G	0.00018125	0.009518	missense, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17882781	TAGGGAGCAGGAGGC[A/G]GCGAGGAATAGGAAC	146691
rs138318777	snp	A/G	0.00517822	0.0506191	intron-variant	TOM1L2	GRCh38.p7	17:17948253	TACCAAGATAAATAC[A/G]CCCTAGTCCCTACCT	146691
rs138318922	in-del	-/CAGA			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17845968	AGTCCCACCCTCAGC[-/CAGA]ACAGAGGTTTCCTCT	146691
rs138342385	snp	C/T	0.00755907	0.0610114	intron-variant	TOM1L2	GRCh38.p7	17:17926368	GTCACCCAGGGTACC[C/T]AGCTAGTTAAGGAGG	146691
rs138379562	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17922834	GGGAAGCAGAAGGGG[A/T]GGGTGACTGTCTCCA	146691
rs138397907	snp	A/G	0.00597247	0.0543191	intron-variant	TOM1L2	GRCh38.p7	17:17852230	TGTAAAAAATAACAC[A/G]ACCTTCACAAAGAAA	146691
rs138437093	snp	A/G	0.00155159	0.0278098	synonymous-codon, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17866363	CATTGGGCTCACCAC[A/G]GCTGGAGACCCTGGC	146691
rs138486187	snp	A/G	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17916773	CACGCCTGTAATCCC[A/G]ATACTTTGGGAGGCC	146691
rs138537592	in-del	-/A			intron-variant	TOM1L2	GRCh38.p7	17:17926176	CTCTGTCTCTTGGAG[-/A]GAAAAAAAAAAAAAA	146691
rs138561612	snp	A/C	0.00398564	0.0444627	intron-variant	TOM1L2	GRCh38.p7	17:17884179	TCTGGATTGATGCTG[A/C]ATACTCACAGCTCAA	146691
rs138614846	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17931420	GCTTATATGCTGTGT[A/G]ATCCTAACCAAATAA	146691
rs138628526	snp	C/T	0.0174175	0.0916809	intron-variant	TOM1L2	GRCh38.p7	17:17968556	AGTAATCCCAGCTAC[C/T]TGGGAGGCTGAGACA	146691
rs138661420	snp	C/T	0.00279162	0.0372561	intron-variant	TOM1L2	GRCh38.p7	17:17850538	TGCTCCCCCAACACT[C/T]CCTCCCCCAAAAAAC	146691
rs138679512	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17922304	CCAGGGCCAGGGCCT[C/T]GGTGAAGGGGAGCGG	146691
rs138683843	snp	C/G	0.0146672	0.084371	intron-variant	TOM1L2	GRCh38.p7	17:17904091	TCCTGCCTCAGCCTT[C/G]TGAATAGGTGGGACT	146691
rs138703159	snp	C/G	0.00279162	0.0372561	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17846242	GGAACCTGTGCTGAC[C/G]TAGGCAGTGCATGCT	146691
rs138737113	snp	G/T	0.0182019	0.0936463	intron-variant	TOM1L2	GRCh38.p7	17:17900086	GGTGTGGTGGCAGCT[G/T]CCTGTAATCCTAGCT	146691
rs138740740	snp	A/G	0.00636936	0.0560724	intron-variant	TOM1L2	GRCh38.p7	17:17951183	TACCCACTCCCTTGC[A/G]GGGCTGCAAGGAAAA	146691
rs138767851	snp	A/T	0.00795532	0.062565	intron-variant	TOM1L2	GRCh38.p7	17:17894306	ACTCAACCCTGCTTC[A/T]GCAACCAAAATTGGC	146691
rs138790403	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17867388	AGGAAGGCGGACGCA[C/T]GGCCCTGGCTACGGC	146691
rs138797183	snp	C/T	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17952033	TAAACTACACAAATA[C/T]AGAAATGCACAAAGA	146691
rs138797627	snp	A/G/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17970043	TATATTTGGTTTTTT[A/G/T]TTGTTGTTGTTGTTG	146691
rs138936813	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17905234	TCCCACGTTTTCATC[C/T]AGTGCAGGCCACTGC	146691
rs138985296	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17880560	TGAAATATCATAGAA[C/G]AATCTGCATAGAGGT	146691
rs138999765	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17966518	TAGAATGCTACTTCC[C/T]ACCCCAAACCTACTG	146691
rs139006036	snp	C/G	0.0154538	0.0865337	intron-variant	TOM1L2	GRCh38.p7	17:17956078	AACATTTGTTTCAAA[C/G]AGCAAAAGAACAAAG	146691
rs139020086	in-del	-/G			intron-variant	TOM1L2	GRCh38.p7	17:17852891	AAAAAAAAAAAAAAA[-/G]AACATTGAATTGAAA	146691
rs139022042	snp	G/T	0.00182696	0.0301686	synonymous-codon, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17898658	GCTTCTTCAGGGCTC[G/T]AATGGCATCCTTTGG	146691
rs139027770	snp	A/G	0.0162398	0.0886349	intron-variant	TOM1L2	GRCh38.p7	17:17871442	TGGGAGGCCGAGGCA[A/G]GCGGATCACTTGAGG	146691
rs139069604	snp	A/G	0.00398564	0.0444627	intron-variant	TOM1L2	GRCh38.p7	17:17883716	TCCAGCCTGGGCGAC[A/G]CAGCAAGACTCCGAC	146691
rs139141212	snp	A/C	0.00149818	0.0273284	missense, upstream-variant-2KB, intron-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17862800	CCGTCACGGGGATTA[A/C]ATTGCTGGAGTGAAC	146691
rs139143017	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17843802	AGGAAATAAATATCC[A/G]TCCCCCTCTCCGGGA	146691
rs139158330	snp	A/C/G	3.29621e-05	0.00405958	missense, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17882748	GTCACACTCAGAGCT[A/C/G]GGGCCTGCGGTGCGG	146691
rs139160414	snp	C/G	0.00398564	0.0444627	intron-variant	TOM1L2	GRCh38.p7	17:17878478	GTGTCAGGCCTGGAA[C/G]AGGTCTCCACCCACC	146691
rs139174546	snp	A/G	0.00318978	0.0398085	intron-variant	TOM1L2	GRCh38.p7	17:17924604	ACCTTGCCTCTACAA[A/G]AAATACAAAATTAGC	146691
rs139257586	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17940606	GGAATAAGGTAAGCC[G/T]GAAAGAATGAAGGAA	146691
rs139274915	snp	C/T	0.0126979	0.078662	intron-variant	TOM1L2	GRCh38.p7	17:17854129	CCAGACACAAAACCT[C/T]AGCTATCTAAACCTC	146691
rs139284272	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17943752	CAGATCTCCCCACTT[C/T]ACTTCAGATAAGGTC	146691
rs139293775	snp	A/G	0.00676609	0.0577691	intron-variant	TOM1L2	GRCh38.p7	17:17953204	AGAACTGCTTGAACT[A/G]GGGAGGCAGAGGTTG	146691
rs139314037	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17869776	TTTCCAGATTGCTTT[A/T]TCTCAACAAAATATT	146691
rs139344560	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17885473	TTCTTTCATGATGTC[C/T]GCTGCCAAAAATGTC	146691
rs139364598	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17934066	AGTGTGCATCACACA[A/T]TAAGTGGGGGGAAAT	146691
rs139382350	snp	A/C	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17900575	GTTTAAGGAGCAAGG[A/C]TACTAGAAGAAAATT	146691
rs139419152	snp	A/G	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17916167	CAAGCTCTACCTCCT[A/G]GGTTCACGCCCTTCT	146691
rs139449587	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17923919	GAGGTGGGCAGATCA[C/T]AAGGTCAGGAGTTTG	146691
rs139494270	in-del	-/CCCAGAGATCTCCTCTTGT	0.132409	0.220618	intron-variant	TOM1L2	GRCh38.p7	17:17867214	CCTCACACACCTGGG[-/CCCAGAGATCTCCTCTTGT]CCCTGGAGGGAGGGT	146691
rs139601088	snp	A/G	0.00279162	0.0372561	intron-variant	TOM1L2	GRCh38.p7	17:17902155	CACTCCAGCCTGGGC[A/G]ACAAGAGCAAAACTC	146691
rs139614444	snp	A/C/G	0.00716625	0.0594738	intron-variant	TOM1L2	GRCh38.p7	17:17874650	TCAGCTTGGAGGAAG[A/C/G]ATGAGCCCCAAGGGC	146691
rs139620019	snp	A/G	0.00517822	0.0506191	intron-variant	TOM1L2	GRCh38.p7	17:17874234	GCTGGGATTACAGGC[A/G]TGAGCCACCACGCCC	146691
rs139661997	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	TOM1L2, DRC3	GRCh38.p7	17:17972789	AGAAACATTTGTTTT[C/G]TCTACGGCTGGTTGG	146691
rs139707382	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17870370	TTGCTTACAGAGCTC[C/T]GTCAATTCCTGCCAG	146691
rs139707511	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17923380	CATTCCAGTCTGGGC[A/G]ACAAGAGTGAAACTC	146691
rs139714452	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17896601	GGGCTGGCAAGAGCC[A/G]CTTTAGGCCACCCTG	146691
rs139744493	snp	A/G	0.0023933	0.0345097	intron-variant	TOM1L2	GRCh38.p7	17:17917999	AGGATGTTTTTCCAT[A/G]TATTTATGTCTTCTT	146691
rs139758979	snp	C/T	0.0349115	0.127424	intron-variant	TOM1L2	GRCh38.p7	17:17914292	CAGGGCACACTGCTG[C/T]CTCAGTGGCTACATT	146691
rs139816500	snp	A/G	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17971815	CATCTCCGAGTCCAA[A/G]TTGGGCCTCAGGGGT	146691
rs139832021	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17844331	CGAGCATCTGTTGCC[C/T]TTGGGCCATGTGGAG	146691
rs139851670	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17929057	AGTCTGAAGATTCCC[C/T]AAGCACTGCTGTGAG	146691
rs139856437	snp	C/T	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17881845	ACTGCCATCCCTACA[C/T]ACACATTGCTATCCC	146691
rs139863160	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17968018	GACTGTGGTCTTAGC[C/T]GCTAACTTGAGATGA	146691
rs139869743	snp	A/G	4.94214e-05	0.00497074	synonymous-codon, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17884664	TATGGGAGACAGAGC[A/G]TCCAAGTCTGCCATG	146691
rs139985939	in-del	-/C	0.0209421	0.100162	intron-variant	TOM1L2	GRCh38.p7	17:17941324	AGGACTGGTCGCAGT[-/C]CCAAGGATGGCACTT	146691
rs140029254	snp	G/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17949453	CTTCCAGCAGCTAGA[G/T]TCTTACAGGATAAAT	146691
rs140040482	snp	G/T	0.00279162	0.0372561	intron-variant	TOM1L2	GRCh38.p7	17:17852535	TTAGGAAGAGTCTGT[G/T]TTGCTCATTATTTCT	146691
rs140047115	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17864026	TGTGTGCCACCACTC[A/G]CAGCTAATTTTTTTG	146691
rs140055594	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17938989	TGGACTAGAATTCCA[C/T]TCTGTCTGACCTCTG	146691
rs140065130	snp	A/G	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17944813	TATTAAATGCTTAGC[A/G]ACAAGGCCTAACAGA	146691
rs140067769	snp	C/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17859512	ACACACAGACACACA[C/G]AGCCCACATGCTCTG	146691
rs140130603	snp	A/G	0.000164965	0.00908048	intron-variant	TOM1L2	GRCh38.p7	17:17848880	GGAGGAGCAGAGAAA[A/G]TGAAATTAGGGCACT	146691
rs140171445	snp	C/T	0.0185938	0.0946107	intron-variant	TOM1L2	GRCh38.p7	17:17871186	CCATCCTGGCTAATA[C/T]GGTGAAACCCCGTCT	146691
rs140193192	snp	G/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17955213	AATCAAGCTGTTCTC[G/T]CCACCTCTTCTATCA	146691
rs140261859	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17888597	CCAGCTACCAGGCTC[C/T]GACGTCTTCAAAGAA	146691
rs140263207	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17954502	ATTTTTAGTAGAGAC[A/G]GGGTTTCGCCATGTT	146691
rs140297730	in-del	-/TG			intron-variant	TOM1L2	GRCh38.p7	17:17891794	CACACGTGTGTGTGT[-/TG]GTGTGTGTGTGTGTG	146691
rs140309393	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17903398	GGAGGCTGAGGCGGG[C/T]GGATCACGAGGTAAG	146691
rs140322756	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17941737	ATTTTACAGTGGAAA[C/T]GGATACATAAGCCCT	146691
rs140327091	snp	A/G	0.00279162	0.0372561	intron-variant	TOM1L2	GRCh38.p7	17:17854282	TGGGAGGCCGAGGAC[A/G]CGCTCCTTGTCAGGC	146691
rs140346442	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17850562	AAAAAACCAAAGCAC[A/G]GCACATACATCTGAA	146691
rs140445913	in-del	-/T	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17870586	GACATGAAGGATAAG[-/T]TCTCTCCTTCTCACA	146691
rs140457102	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17917383	TTGTTTGGCTATTTG[A/G]GGTCCCTTGAGATTT	146691
rs140518090	snp	A/G	0.00636936	0.0560724	intron-variant	TOM1L2	GRCh38.p7	17:17931033	TATAAAATATAAAAT[A/G]TTCTTCCTGTAACTT	146691
rs140547924	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17915107	AGGATACTTCCAGCC[C/T]GTACAGAGGTCTTCT	146691
rs140557624	in-del	-/AAGT	0.0607341	0.163335	intron-variant	TOM1L2	GRCh38.p7	17:17902938	AGACACAGGGAGATG[-/AAGT]AAGTAACTCACACAG	146691
rs140588105	snp	C/T	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17960534	GTAGAGACGGAATTT[C/T]GCCATGTTGCCCAGA	146691
rs140637306	snp	A/G	0.0023933	0.0345097	intron-variant	TOM1L2	GRCh38.p7	17:17926211	AGGTACAAGCTTTCA[A/G]GCTGGCCTAAACATA	146691
rs140644692	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17919869	ATCCCACGCCCCAGC[C/T]GCCAGGAAGGTTCTC	146691

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