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
rs140667386	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17968477	CAAGACCAGCCTGGC[C/T]AAGGTAGTGAAACCT	146691
rs140667401	snp	G/T	0.00795532	0.062565	intron-variant	TOM1L2	GRCh38.p7	17:17916629	ATTCCATTGGTCCAT[G/T]TGTCTTTCCTTATTC	146691
rs140681069	snp	A/G	0.00517822	0.0506191	intron-variant	TOM1L2	GRCh38.p7	17:17934951	CATTACTCAGCCACC[A/G]TGCTGCACTCAGCTA	146691
rs140710606	snp	A/G	0.0023933	0.0345097	intron-variant	TOM1L2	GRCh38.p7	17:17964461	GAGAAGATGAAGAGT[A/G]AAATACAAAAGTATT	146691
rs140719992	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17865255	TCCTGTTTCCAAGCC[C/T]TCTGTAGATATTGAC	146691
rs140812484	snp	C/T	0.00199481	0.0315187	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17846208	GCCAGGTGGGAAGGG[C/T]TAACTACACCATGGA	146691
rs140921961	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17849391	ACAGCACAGGGCCTG[C/T]CACTCAGTAGGTACT	146691
rs140960352	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17891757	GTGGTAGAGTGGGGT[A/G]TATGAGGAAGGTAAA	146691
rs140973573	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17897014	TGGCTGGGTTTGTAG[C/T]GAAGACCTAACCCAA	146691
rs141013293	snp	C/G	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17945153	TGCAAAAGTCTTTAG[C/G]TTTCTTTTCAGAGAT	146691
rs141013373	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17893575	CATTTTTTTTTTCCT[C/T]CAAATGGTGGGAGAG	146691
rs141092559	snp	A/G	0.00159617	0.0282053	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17860493	AAGAAGGAGCATCCC[A/G]TGGAAACCAGCACTG	146691
rs141105694	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17942287	TTGCAAGGTTCCATT[A/G]ATAAATAGCAGTAAT	146691
rs141162979	snp	C/T	0.00795532	0.062565	intron-variant	TOM1L2	GRCh38.p7	17:17942930	ACAAAAAGCTGTTTA[C/T]CTTTTAGAGCCCTTT	146691
rs141164116	in-del	-/GGGGGGGGGG			intron-variant	TOM1L2	GRCh38.p7	17:17919204	TCTCACACAGTGGCT[-/GGGGGGGGGG]GTTAGAGGAGACTAA	146691
rs141171530	in-del	-/T			intron-variant	TOM1L2	GRCh38.p7	17:17911646	ATTAGCTGGAAATTC[-/T]TTTTTTTTTTTAATT	146691
rs141184752	in-del	-/T	0.0607341	0.163335	intron-variant	TOM1L2	GRCh38.p7	17:17893513	CCAGTGGGATGAGAA[-/T]TTTTTTTGAAGTATT	146691
rs141225500	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17904441	AGAATTTCAAGCTGG[A/G]CCCAGGAATATGGAA	146691
rs141301017	snp	C/G/T	0.000148343	0.00861112	synonymous-codon, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17850941	CATGACAGATGGCTG[C/G/T]GCAACGGGGATCTAT	146691
rs141334726	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17876454	GTGGGGCTTATGGCA[A/G]TCTTCAAATATTTAA	146691
rs141337186	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17880108	GCTTCCGTTCCTGCT[C/G]TTTAAAATCCAAGTG	146691
rs141353505	snp	A/G	0.0356815	0.128715	intron-variant	TOM1L2	GRCh38.p7	17:17871288	AGGCAGGAGAATGGC[A/G]TGAACCCAGGAGGCG	146691
rs141375393	snp	A/C/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17927542	TAAACATTTGGCCTC[A/C/G]TGAGAATGGCCACAG	146691
rs141381396	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17894492	TGGTTCTGGCCAGAC[A/G]GTCAGTGAGAGCTTG	146691
rs141416225	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17867776	GACAAGAAAGAGATC[C/T]CCAGGAGGAATGATC	146691
rs141417765	snp	A/G	0.0154538	0.0865337	intron-variant	TOM1L2	GRCh38.p7	17:17864581	CAGTGGCACAATCTC[A/G]GCTCACTGCAACCTC	146691
rs141462803	snp	C/T	0.00358779	0.0422022	intron-variant	TOM1L2	GRCh38.p7	17:17917020	CATAAATTAGCTGGG[C/T]GCAGGGGCACACACC	146691
rs141512497	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17891856	GAAGGATATTGGGTG[A/G]GCAGAACAGGGACGA	146691
rs141524395	snp	C/T	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17861924	TAATTCTTATTTTAT[C/T]AGCAGCAGCCTCAGT	146691
rs141532435	snp	A/C	0.00279162	0.0372561	intron-variant	TOM1L2	GRCh38.p7	17:17947249	TGCTGGTCTTGAACT[A/C]CTGGGCTCAAGTGAT	146691
rs141551894	snp	A/G	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17887359	ATGGGGTGCAGGGGC[A/G]CCTCTGAATAAATGC	146691
rs141610547	snp	A/G	0.00636936	0.0560724	intron-variant	TOM1L2	GRCh38.p7	17:17851356	CCACTATGACAGTCC[A/G]CTGTCAAGCCCAACC	146691
rs141629879	snp	A/G	0.0162398	0.0886349	intron-variant	TOM1L2	GRCh38.p7	17:17898220	TGAGTCACCGCGCCT[A/G]GCCAACATTTTTACA	146691
rs141755585	in-del	-/T			intron-variant	TOM1L2	GRCh38.p7	17:17928172	AACAAAAAAAATCAG[-/T]AGGAGACAGCATAAA	146691
rs141811470	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17970893	AGTCCTTCAACCAAC[C/T]AGGAGGAATCCAGTT	146691
rs141841081	snp	C/T	0.0126979	0.078662	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17844814	AGAAAGGGTTAAACA[C/T]ATTCCCAAGAAAATA	146691
rs141848214	snp	C/T	0.00358779	0.0422022	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17846711	AGATGTGTGAGGCTA[C/T]GGCAGGCCAGGCCAC	146691
rs141872961	snp	C/T	0.0372196	0.131242	intron-variant	TOM1L2	GRCh38.p7	17:17957879	GCGGATCATGAGGTC[C/T]GGAGATCAAGACCAT	146691
rs141888342	snp	C/T	0.00557542	0.0525036	intron-variant	TOM1L2	GRCh38.p7	17:17873521	GCCTCAAGGGTGGTT[C/T]ACTGGATTTAGAGGA	146691
rs141957116	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17904745	CCTCCCGCTCCCCCA[A/G]TGTCACCCTGTCTAT	146691
rs141965541	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17951072	AGGTAAGGGCTTTAG[C/T]GTGGGGCAGACCTGT	146691
rs141970880	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17952202	CCAAAATGTACAATG[A/G]CATGGCAAAACAAAA	146691
rs141977420	snp	A/C	0.00318978	0.0398085	intron-variant	TOM1L2	GRCh38.p7	17:17951613	CAAAGGGTTTTTAGC[A/C]AAAAACCTTTCAAGA	146691
rs142050683	snp	A/G	0.0111196	0.0737302	intron-variant	TOM1L2	GRCh38.p7	17:17946781	CCAGGCTGGAGCGCA[A/G]TGGCACAATCTTGGC	146691
rs142070589	snp	A/G	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17871071	TTAATTAATGACTCT[A/G]AAGTATTCAGAGGCC	146691
rs142091065	snp	A/G	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17919705	GTTTCTTGCCCTTAA[A/G]GCTACCATTGAACCA	146691
rs142157164	snp	C/T	0.00636936	0.0560724	intron-variant	TOM1L2	GRCh38.p7	17:17950409	AGTGATCTGCCTGCC[C/T]TAGCCTCCCAAAATG	146691
rs142177592	snp	C/T	0.0236746	0.106192	intron-variant	TOM1L2	GRCh38.p7	17:17864456	ACCTTGTGATCCACC[C/T]GCCTCGGCCTCCCAA	146691
rs142249750	snp	C/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17908802	ACAAGTGTTGGCAAG[C/G]ATATAGACAAATTGG	146691
rs142277648	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17905416	ATTTCCCTTAACTCT[C/T]CATTCCTGTCTTATG	146691
rs142325996	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17883313	GCAATTTACCAAATG[C/T]TTTTTGTAATTATAG	146691
rs142344542	snp	A/G	0.00517822	0.0506191	intron-variant	TOM1L2	GRCh38.p7	17:17929924	CAGCAAGGCAGCTGC[A/G]ATGAGTGAGGTACTA	146691
rs142364551	snp	C/T	0.0209421	0.100162	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17859733	TAAAAACACAAAAAT[C/T]AGCCGGCTGTGGTGG	146691
rs142374476	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17931909	TGCAAATCACATTAA[C/T]ATAACCCGAGGTGGC	146691
rs142424594	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17926380	ACCCAGCTAGTTAAG[A/G]AGGACCAAACTGAGA	146691
rs142432222	snp	C/T	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17926064	TAGTCCCAGCTACTC[C/T]ACAGGCTGAGGTGAG	146691
rs142473918	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17853244	TCTCCAGAGAGAAAA[C/T]AGTCCCACACTAGCG	146691
rs142479417	snp	G/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	TOM1L2, DRC3	GRCh38.p7	17:17973997	GGTTGGGTGGTAAAC[G/T]ATAAGATCCCCATAG	146691
rs142500519	in-del	-/G	0.0923359	0.194016	upstream-variant-2KB, intron-variant	TOM1L2, DRC3	GRCh38.p7	17:17973605	TTTATTCTTTTTTAA[-/G]AAAAATTTTGTTCAT	146691
rs142502409	snp	C/T	0.00318978	0.0398085	intron-variant	TOM1L2	GRCh38.p7	17:17916263	TATTTTTAGTAGAGA[C/T]GGGGTTTCACTGTGT	146691
rs142515051	snp	A/G	1.64838e-05	0.00287083	missense, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17882727	GAATTGGCTGTGATG[A/G]GGCCAGTCACACTCA	146691
rs142548610	snp	A/G	0.0325976	0.123435	intron-variant	TOM1L2	GRCh38.p7	17:17962528	CGTGTTGCGCAGGCT[A/G]GTCTCGAACTCCTGA	146691
rs142558539	snp	C/T	0.00835141	0.0640778	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17843813	ATCCGTCCCCCTCTC[C/T]GGGAGAGCCTGGAGG	146691
rs142579355	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17890656	AGGCAACAGAGCACT[C/G]TGGATGAAGTTCAGG	146691
rs142581994	snp	C/T	0.000153988	0.00877328	missense, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17882848	TGGTCGCAGCTGGAT[C/T]CACTTCAGGGACACT	146691
rs142618280	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17886249	AATTATGACTGATGC[A/G]TCTCACCAGGAACAG	146691
rs142623965	snp	A/C	0.00953873	0.0683987	intron-variant	TOM1L2	GRCh38.p7	17:17907740	GAGGTTCTTCATTCA[A/C]CAAACTCTAGACTGA	146691
rs142659717	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17889469	GGAGCCCAACCTCCC[C/T]CTTCCCCTCAATCTG	146691
rs142680733	in-del	-/AAACAA	0.031825	0.122064	intron-variant	TOM1L2	GRCh38.p7	17:17924137	GCAAGACTCTGTCTC[-/AAACAA]AAACAAAAACAAAGG	146691
rs142696068	snp	A/C	0.00358779	0.0422022	intron-variant	TOM1L2	GRCh38.p7	17:17884533	AGAAAGCATGATGAC[A/C]AGCTGAATAATTCAA	146691
rs142748902	snp	A/G	0.00398564	0.0444627	intron-variant	TOM1L2	GRCh38.p7	17:17852328	CTGATGGTGGGGGAG[A/G]GTGGTTTGGGGTCCC	146691
rs142783691	snp	A/G	0.0607341	0.163335	intron-variant	TOM1L2	GRCh38.p7	17:17913511	AAATTCTTTTATGAA[A/G]AGAAAAATCAGAACT	146691
rs142811474	snp	C/G	0.00636936	0.0560724	intron-variant	TOM1L2	GRCh38.p7	17:17944452	ACCGACAGCTTGACG[C/G]TCCCTTCACCTCCAT	146691
rs142813134	snp	A/C	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17970576	AGGACATGGGGAAGA[A/C]GTAAGGAAGTGAGAA	146691
rs142813882	snp	C/T	0.00478085	0.0486577	intron-variant	TOM1L2	GRCh38.p7	17:17917502	CAGGGTCTTGCTATG[C/T]TGCCCAGTCTGGACT	146691
rs142843986	snp	A/G	0.00438332	0.0466095	intron-variant	TOM1L2	GRCh38.p7	17:17966110	TGGGCAACAGAGCAA[A/G]ACTCCATCTGGAAAA	146691
rs142990508	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17896219	CCCTTCTCTCTAGGA[C/T]TCTCTAAAACCTTCC	146691
rs143054062	snp	A/C/G	3.29556e-05	0.00405918	intron-variant	TOM1L2	GRCh38.p7	17:17866848	GGTCTGGCCTCAGGA[A/C/G]ATGACAGGATTCTGA	146691
rs143069395	snp	C/T	0.00181123	0.0300389	synonymous-codon, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17882756	CAGAGCTGGGGCCTG[C/T]GGTGCGGAGTAGGGA	146691
rs143094992	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17863441	GAAAGGCAGATAAAA[A/C]GGCACGGGGTTTGGA	146691
rs143095039	snp	C/T	0.0607341	0.163335	intron-variant	TOM1L2	GRCh38.p7	17:17916883	CAAAAATTAGCCAGG[C/T]ACAGTGGCTCACACC	146691
rs143100611	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17861155	AACAGCAGGGGTTCT[A/G]GAAATGGACACTAAT	146691
rs143105134	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17883798	GATGACCTCTTGCAC[A/G]TTAAAATTAAGTCGT	146691
rs143141192	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17965668	GACCTTAGGTAGGTT[C/T]CATACTTTCTCATTG	146691
rs143148030	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17879248	AGTACAAGCTCAACT[A/G]CATTTAAAATAAACC	146691
rs143182667	snp	A/T	0.000675214	0.0183617	synonymous-codon, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17866906	TTGAACGGATCGGCC[A/T]GACCTGTATCGTTCG	146691
rs143190643	snp	A/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17942422	CTCAATCATATCATA[A/T]GTAAAATGGGGATTA	146691
rs143218625	snp	A/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17971819	TCCGAGTCCAAGTTG[A/G]GCCTCAGGGGTGCCT	146691
rs143220830	snp	A/G	0.0020899	0.032258	missense, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17884689	GCCATGGGAAATTCA[A/G]CCCCTTTCCTCTTCA	146691
rs143225227	snp	C/T	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17916991	ATGGTGAAACCCCAT[C/T]TCTACTAAAAATACA	146691
rs143228017	snp	A/G	0.0142736	0.0832652	intron-variant	TOM1L2	GRCh38.p7	17:17885344	CTAGCTCTGTCTAGC[A/G]CTGCTGCCAGTAGGT	146691
rs143267389	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17845834	CAAGCATCAGGGAGC[A/T]GAAGGCCCAGGCAGG	146691
rs143273074	snp	C/T	0.0142736	0.0832652	intron-variant	TOM1L2	GRCh38.p7	17:17965457	TTTTCCATTTCTACA[C/T]AAACCAAATCCTCCC	146691
rs143285665	snp	C/T			intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17860880	CTGTGCCGCACCCCC[C/T]CACCGCCACAGGACA	146691
rs143297465	snp	C/T	0.00279162	0.0372561	intron-variant	TOM1L2	GRCh38.p7	17:17881979	TTTTTTTCCCCCAAG[C/T]CTGACCAATTCTCAA	146691
rs143309642	snp	A/G	0.0115144	0.0749975	intron-variant	TOM1L2	GRCh38.p7	17:17968282	AGACAAAATTATTTA[A/G]GTGTAAGCCCCATGC	146691
rs143313370	snp	G/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17893123	ATACAACCCAAATAT[G/T]CCAACTGCTCTCTTT	146691
rs143501362	in-del	-/ACACAC			intron-variant	TOM1L2	GRCh38.p7	17:17945268	ACCACACACACACAT[-/ACACAC]ACACACACACACACA	146691
rs143521789	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17861150	GTAGGAACAGCAGGG[A/G]TTCTGGAAATGGACA	146691
rs143561964	snp	A/G	0.00517822	0.0506191	intron-variant, downstream-variant-500B	TOM1L2, LOC100507131	GRCh38.p7	17:17858187	CTTTTCAAAGAACCA[A/G]CTTTTACAAAAGCAA	146691
rs143607027	snp	C/T	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17901603	TTCTCCTCATCACCC[C/T]CAAGGAGGACATGGC	146691
rs143625645	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17897895	ACAGTCCCAGGCAGG[C/G]GCAGGTACTCAATAG	146691
rs143643996	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17949692	GAAGGACAGAAGCAA[C/T]GGCCAGAAGGCTGGT	146691
rs143646997	snp	C/T	0.00557542	0.0525036	intron-variant	TOM1L2	GRCh38.p7	17:17958544	ATGACAGACTTACTA[C/T]CCCATGCTTACCCTC	146691
rs143654934	snp	C/T	0.0356815	0.128715	intron-variant	TOM1L2	GRCh38.p7	17:17874258	CACGCCCAGCCATTA[C/T]TTATTTATTTATTTA	146691
rs143683494	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17887439	CGTACAGATGGGAGA[C/T]ATCCAGAGATGCCAT	146691
rs143694764	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17922825	ATTCCAGCGGGGAAG[C/T]AGAAGGGGAGGGTGA	146691
rs143740637	snp	A/G	0.00478085	0.0486577	intron-variant	TOM1L2	GRCh38.p7	17:17944929	CCTCCATTTTTCATA[A/G]GCCGGATGCTCCTGC	146691
rs143752965	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17951381	TCTCACTTTGTCTTA[C/T]TGGGTTAGAGATGAA	146691
rs143754531	snp	G/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17866032	CGGGCGTGAGCCACT[G/T]CGCACGGCCGTGACC	146691
rs143793320	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17883223	ATTAAGTTTTGCTAA[C/T]CACAGATCTTTACTT	146691
rs143816562	snp	A/G	1.64972e-05	0.00287199	stop-gained, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17879710	CTTTTGTGTTTCCTC[A/G]AACGACGTCCAGTTC	146691
rs143836593	snp	C/G	0.00755907	0.0610114	intron-variant	TOM1L2	GRCh38.p7	17:17878014	GAGCACGGCTCTATC[C/G]AGAGCAAATCCCCCC	146691
rs143886787	snp	C/T	0.0182019	0.0936463	intron-variant	TOM1L2	GRCh38.p7	17:17967761	TATACGCGCGTGCCA[C/T]CATGCCCAGCTAATT	146691
rs143933572	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17848092	GGGGTGGGGCAGGGT[A/C]AGCTGGAGGGGCCAG	146691
rs144000106	snp	A/G	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17881260	GCTAGGAAGGCCCAG[A/G]AAGGCTATGGGCAGC	146691
rs144010877	snp	C/T	0.0023933	0.0345097	intron-variant	TOM1L2	GRCh38.p7	17:17939078	ATAAAATGAAGAACC[C/T]TGATATACAGACAGC	146691
rs144019168	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17875474	TCTTTGGGCCTAAGA[C/T]ACCCAAGAGCCTACT	146691
rs144019597	snp	A/G	0.0023933	0.0345097	intron-variant	TOM1L2	GRCh38.p7	17:17928093	TAGAAGCTCAATGAT[A/G]AGTATGTGGGGGTTC	146691
rs144061121	snp	C/T	1.64814e-05	0.00287061	missense, intron-variant	TOM1L2	GRCh38.p7	17:17862833	AGGGTGCCACTGACG[C/T]TCTCTGTCCCCAAGT	146691
rs144067613	snp	A/G	0.00517822	0.0506191	intron-variant	TOM1L2	GRCh38.p7	17:17924709	GACTGAGGCTGCAGC[A/G]AACCGTGATCACATC	146691
rs144108947	snp	A/G	0.00279162	0.0372561	intron-variant	TOM1L2	GRCh38.p7	17:17926631	AGTTTTGGAGGCCGA[A/G]GCGGGCGGATTGCTT	146691
rs144186572	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17954886	CACACAGATACTACG[C/T]TCTAAGGCCAAGAGA	146691
rs144215401	snp	A/G	0.00159617	0.0282053	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17859159	TCGGCTCACTGCAAC[A/G]TCCGCCTTTGGGTTC	146691
rs144251630	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17854130	CAGACACAAAACCTT[A/C]GCTATCTAAACCTCT	146691
rs144253677	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17906816	TGGTTTAAGAGGGCA[C/T]GGCTACAGTAAAGTA	146691
rs144286969	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17906848	GTGTTAGTGGTATGG[A/T]CAGAGGGCTAAATAC	146691
rs144342105	snp	G/T	0.00478085	0.0486577	intron-variant	TOM1L2	GRCh38.p7	17:17848493	GCCCAAGGGTGCTGC[G/T]GCGCACCTCCACAAA	146691
rs144347240	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17902583	GTTGGGGGTAGGGGG[C/T]GCTGCTTGTGATGAT	146691
rs144373290	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17852984	ACTGGGGGGATGGAC[A/G]CACAAATGACTGACA	146691
rs144393419	snp	C/G	0.00358779	0.0422022	intron-variant	TOM1L2	GRCh38.p7	17:17901156	AGTGATGGGTGAGCA[C/G]AAAAGCAAGTATTTA	146691
rs144478072	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17890167	AAGGGGCTAAAAAAA[C/G]GTTGACCCAATGCAA	146691
rs144497916	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17938833	CCACCTTGGCCTCCT[A/G]AAGTACTGGGATTAT	146691
rs144541510	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17953680	CCAGCCCAACACACA[A/T]GAAGACACATGAGTG	146691
rs144564501	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17908814	AAGGATATAGACAAA[C/T]TGGAACCCCTTTACA	146691
rs144566098	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17970754	CAATAAGTTTATAGG[C/T]TCCACTAAAGGCTGG	146691
rs144566546	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17960961	CTTAAAACTTTTGTG[C/T]ATTAAAGGACACTAT	146691
rs144585778	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17884510	AAAAGGAATGCCCCC[A/G]AGCTTTAAGAAAGCA	146691
rs144591677	snp	A/G	0.00102125	0.0225739	missense, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17882823	CTCTGCTGTGATTGG[A/G]ACCTGGGCATGGTCG	146691
rs144605645	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17935053	GAGGAACCAAAATGC[A/G]CAAGACCCCACAGCA	146691
rs144669335	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17873049	CAGACTTTCCAGAAT[A/G]TAGGTGGCCTCAGGC	146691
rs144737546	snp	C/T	0.0611083	0.163768	intron-variant	TOM1L2	GRCh38.p7	17:17864311	CGCCTCCCGGGTTCA[C/T]GCCATTCTCCTGCCT	146691
rs144761420	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17897042	CAAGGAAAGGTCAAA[C/T]AGTGTCCATCATGCC	146691
rs144763450	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17846227	CTACACCATGGATCA[A/G]GAACCTGTGCTGACC	146691
rs144840537	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17943916	CTCCAATGTTCTCTC[C/T]TCCTTGCACATCCCT	146691
rs144846487	snp	A/G	0.000798403	0.0199641	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17858732	GGATTACAAGCATGC[A/G]CTGCCACGCCCAGCT	146691
rs144853541	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17894183	TATAAGGCATTAGCC[A/G]ATCGGACATGGGCTC	146691
rs144889402	snp	A/G	0.00676609	0.0577691	intron-variant	TOM1L2	GRCh38.p7	17:17918433	GTGAAAGGCAGCATC[A/G]TTGCGCCTATATATA	146691
rs144970186	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17940172	CATTCCAGGCTGGGC[A/G]ACAGAGCAAGACTCT	146691
rs144974516	snp	C/T	0.00517822	0.0506191	intron-variant	TOM1L2	GRCh38.p7	17:17886834	GTTCACAGAGACAGA[C/T]TGGAGTGGGAGGGAA	146691
rs145020428	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17855479	ACCAGCCAAGAGAGG[C/T]AAAAAGACCTCACAC	146691
rs145096522	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17963465	TGGCTGGAGAGGACC[A/G]CTCCGCCTACTTGAG	146691
rs145100280	in-del	-/CT	0.0019992	0.0315532	intron-variant	TOM1L2	GRCh38.p7	17:17878029	CAGAGCAAATCCCCC[-/CT]GTCAGCAGGAATTCC	146691
rs145116893	snp	A/G	0.00438332	0.0466095	intron-variant	TOM1L2	GRCh38.p7	17:17876981	AGTGGAGGATTTGAC[A/G]CATAGCTCAAGAGGA	146691
rs145137404	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17871358	ACTGGGAGAGAGAGC[A/G]AGACTCCATCTCAAA	146691
rs145143504	snp	A/G	0.00279162	0.0372561	intron-variant	TOM1L2	GRCh38.p7	17:17955992	TCTGCGCCAGCCTCA[A/G]GAGAAAAACTGCAGA	146691
rs145163933	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17951770	AGGAAGGAAGTTAGC[C/T]GAAGGCAACTTTCAT	146691
rs145212794	snp	A/G	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17892278	AGCCCGGCCTGCCCC[A/G]GCACTCCACTTCCTG	146691
rs145261583	snp	C/T	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17941093	GCTACTGGAGACCAT[C/T]TCTCCAGTGAACAGG	146691
rs145272969	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17954080	ACTGCAGTTCAGAGG[C/T]TTCTGGGCCAGCTTT	146691
rs145275066	snp	A/T	0.00398564	0.0444627	intron-variant	TOM1L2	GRCh38.p7	17:17870709	CATATTGTCTCATAA[A/T]CTTGCTAGCTTGGCT	146691
rs145295489	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17955442	CTCCCGGGTTCAAGC[A/G]ATTCTCCAGCCTCCA	146691
rs145372848	snp	G/T	0.0185938	0.0946107	intron-variant	TOM1L2	GRCh38.p7	17:17885917	GCGACAGAGCAAGAC[G/T]CCGTCTCAAAAAAAA	146691
rs145393131	snp	A/G	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17871231	AAAAATTAGCCGGGC[A/G]TTGGTGGCGGGCACC	146691
rs145420007	snp	A/G	3.30022e-05	0.00406202	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17907514	CCTCACTTTGCAGGG[A/G]GCCATCTGTTGCCTT	146691
rs145438922	snp	A/C/G	0.00362486	0.0424185	stop-gained, synonymous-codon, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17869345	CGGCTCCCACCTCTC[A/C/G]TATCGAAGGAAGACG	146691
rs145458248	snp	A/G	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17875275	AGAAAAAAAGAAAAA[A/G]AAAAAAAAAGGACAG	146691
rs145467981	snp	A/G	0.0023933	0.0345097	intron-variant	TOM1L2	GRCh38.p7	17:17854542	TTAATTAATTTATTT[A/G]GAGACAGAGTCTTGC	146691
rs145512816	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17850621	TGTGTGTTTTGGAGC[C/T]AGCTACGGCTAGGAC	146691
rs145529301	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17937303	CTATTCAAGGAACAC[C/T]GACATTTTTATTTTT	146691
rs145556777	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17852932	GAGTCTTATCACCCA[C/G]ACATGAAACCTAGGG	146691
rs145614479	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17934273	AACATAGTGAGACTT[C/T]GTCTCTACAAAAACA	146691
rs145626175	snp	A/G			intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17860280	AGAATCAGAGCCATG[A/G]GCACTGCATTGATTT	146691
rs145649442	snp	A/T	0.0023933	0.0345097	intron-variant	TOM1L2	GRCh38.p7	17:17849018	TTTCTGTAATAGTAA[A/T]ATACTGCTCTTCTTA	146691
rs145687907	snp	A/G	0.00676609	0.0577691	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17844946	ATTTCTAACACTCAC[A/G]GAGAGGCTGGTGGGC	146691
rs145706137	snp	C/T	0.00795532	0.062565	intron-variant	TOM1L2	GRCh38.p7	17:17929531	AGCTACTCAGGAGGC[C/T]GAGGCAGGAGAATCG	146691
rs145722244	snp	C/T	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17935981	CCATCCTCCACCCAG[C/T]AGCTAGTGGCTTTTC	146691
rs145741752	snp	A/G	0.0023933	0.0345097	intron-variant	TOM1L2	GRCh38.p7	17:17850370	CTATCTCTGAGGATG[A/G]AGACAATGGGTCTTT	146691
rs145808881	snp	C/G	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17882406	AGCATGCGGTCTCAC[C/G]TGACAAAGCCCAACT	146691
rs145828753	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17929184	TGGCTGCTCAGCAGC[A/G]TCAGGCGGGGAAGTC	146691
rs145839429	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17900040	AACATGGTGAAACCC[C/T]GTCTTTACTGAAATA	146691
rs145868968	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17916670	ATGTTGTGATTATTA[C/T]AGTTTTGAAGTAAGT	146691
rs145877547	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17946984	CCCTCCTCAGCCTCC[C/T]AAAGTGCTGGGATTA	146691
rs145932831	snp	A/G	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17884979	ATGGTGCTGCTGAGC[A/G]TGAACAAAAACACAA	146691
rs145959115	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17933468	CAGGTATTGGGAGCC[C/T]GTGGAACAGTGTCTA	146691
rs145970344	snp	A/T	0.0023933	0.0345097	intron-variant	TOM1L2	GRCh38.p7	17:17928617	ATGAATTAATTGCAC[A/T]CTTCTGGGATCTCAC	146691
rs145989079	snp	C/T	0.000247095	0.0111124	synonymous-codon, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17884658	TGTGTGTATGGGAGA[C/T]AGAGCGTCCAAGTCT	146691
rs146033716	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17889538	GGGGCAGTGGGCTTT[A/G]GCCAGCAGCTGGTAA	146691
rs146057546	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17949381	CTCTGACAAGAGCCT[A/G]TCTCAGCCCCCAAGG	146691
rs146071694	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17944680	TTTTATTTAACATAG[C/T]ATAAAACCAACGTCT	146691
rs146148202	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17951522	TGGCAACAGAAAAAT[C/T]TGGTTTCCTCAGGAG	146691
rs146181297	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17927777	CAAGTGAGCCTCCCA[C/T]CCTCAGCCTCCTGAG	146691
rs146192005	snp	C/T	0.0333695	0.124785	intron-variant	TOM1L2	GRCh38.p7	17:17924207	ATAAAATGTCCAGAA[C/T]AGGCAAATCTATAGA	146691
rs146285322	snp	A/G	0.00318978	0.0398085	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847498	AGTGGGAGGCCTGGG[A/G]GCAGACACGGTGGCA	146691
rs146301377	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17905505	ATCATCTCACACCAG[G/T]ATTACTGTGATAACC	146691
rs146312145	snp	C/T	0.00597247	0.0543191	intron-variant	TOM1L2	GRCh38.p7	17:17952328	GGAGCCTAGTTGGGC[C/T]GAGAAATTAAGGGCT	146691
rs146339075	snp	A/G	0.0633504	0.166319	intron-variant	TOM1L2	GRCh38.p7	17:17949964	CAAGCTCCGCCTCCC[A/G]GGTTCACACCATTCT	146691
rs146443731	snp	A/C	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17881507	AACTTCAAACATTTT[A/C]TGCCTTCCCTCAGAG	146691
rs146446650	snp	C/T	4.21914e-05	0.00459281	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17866341	ATGGGGGCGCTGTGT[C/T]CCCCACCATTGGGCT	146691
rs146454571	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17875887	TAATGAAGCTAAACA[C/T]GTAGAATAAACTAGA	146691
rs146474832	snp	C/G	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17945083	ACCAAAATAGCTCAT[C/G]TGACCTTTGCAAATA	146691
rs146500299	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17941963	ACCTCATCTCTAAAA[C/T]ACAAAAGTCTCAGCC	146691
rs146502059	snp	A/C	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17878426	AAGCTCCAGGGACCA[A/C]AGCTCATGCACCTCT	146691
rs146542892	in-del	-/AGAG	0.0232847	0.105357	intron-variant	TOM1L2	GRCh38.p7	17:17886825	TGCTTCCATGTTCAC[-/AGAG]ACAGACTGGAGTGGG	146691
rs146566341	snp	A/G	0.0356815	0.128715	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17859327	TGATCCGCCCGCCTC[A/G]GCCTCCCAAAGTGCT	146691
rs146572034	snp	A/T	0.0023933	0.0345097	intron-variant	TOM1L2	GRCh38.p7	17:17926481	ACAATAGGGTTCTAG[A/T]TCATCTGGGAAATTA	146691
rs146578360	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17854152	TAAACCTCTTGTCCT[A/G]GTAAATAAATGCCTT	146691
rs146604032	snp	A/G	0.00636936	0.0560724	intron-variant	TOM1L2	GRCh38.p7	17:17925149	AGTACTATGCTTCCT[A/G]TACAGCCTGCAAAAC	146691
rs146614581	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17920528	TATTTTTAGTAGAGA[C/T]GGGGTTTCACAATGT	146691
rs146710625	snp	G/T	0.000494381	0.0157145	missense, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17882728	AATTGGCTGTGATGG[G/T]GCCAGTCACACTCAG	146691
rs146724090	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17903102	CAAGAAGGCTTTGCT[A/G]CCAAAAGTCCCAAGG	146691
rs146735480	snp	A/G	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17897376	CTTAATAAGTTTTGG[A/G]GTTTCGCTTGGGCAA	146691
rs146797713	snp	A/G	0.00517822	0.0506191	intron-variant	TOM1L2	GRCh38.p7	17:17901606	TCCTCATCACCCCCA[A/G]GGAGGACATGGCTGC	146691
rs146823737	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17896962	GCCTCAGTGTAGGGA[C/T]GGCAGCCCTGCGCAT	146691
rs146834113	snp	A/G	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17968337	AAGCAGGGAAAATTA[A/G]GTCCAAAGAGACTAA	146691
rs146860871	snp	A/C/G	0.00478085	0.0486577	intron-variant	TOM1L2	GRCh38.p7	17:17963916	TTATCTCATTTAATC[A/C/G]TCACAAAAACCTGGA	146691
rs146927292	snp	C/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17860583	GCAAACAGCCCTTTG[C/G]AAACCTTCCTGTCCA	146691
rs146944644	snp	A/G	0.00318978	0.0398085	intron-variant	TOM1L2	GRCh38.p7	17:17857593	GGGAATCTGTGGCTT[A/G]CAGAGATTATGCAAA	146691
rs146967942	snp	C/G	0.0232847	0.105357	intron-variant	TOM1L2	GRCh38.p7	17:17904443	AATTTCAAGCTGGGC[C/G]CAGGAATATGGAAAA	146691
rs146989195	in-del	-/CCTGC	0.0704125	0.17392	intron-variant	TOM1L2	GRCh38.p7	17:17911296	TTACCCGAGCTCAGG[-/CCTGC]CCTGCCCTGTCCAGT	146691
rs147030540	snp	C/G	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17926325	TCTGACCAGGCCTCC[C/G]TGCTAACTCTCCCTT	146691
rs147187584	snp	C/T	0.030665	0.119967	intron-variant	TOM1L2	GRCh38.p7	17:17879533	GCCACTGGACCTGTC[C/T]CGCCTTGCCGCTGTG	146691
rs147202020	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17959839	CCAGACTACAAGGCT[C/T]ATGCTTCATTAATGA	146691
rs147275011	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17873740	TCCAAGTCTCCAGTC[C/T]TCTCCAGGCCTGCTT	146691
rs147297445	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17943705	AAACAGAAAATCTGA[C/T]CTCATCTTCCCCCTA	146691
rs147388488	snp	C/T	0.00438332	0.0466095	intron-variant	TOM1L2	GRCh38.p7	17:17852376	CTGAGCAGGTATCTA[C/T]GATGCCACCAGAGCT	146691
rs147404282	snp	A/G	0.00438332	0.0466095	intron-variant	TOM1L2	GRCh38.p7	17:17870212	CGAAAGAGGAAATTC[A/G]CACACCCCCGGTTGC	146691
rs147448880	snp	C/T	6.62361e-05	0.00575445	synonymous-codon, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847710	GGCTGGGGCAGGAGC[C/T]TCCATGGGGGGCGAG	146691
rs147504636	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17848592	CAGCTCTGCAACTTT[A/G]TGGAATTGACATGTT	146691
rs147552379	snp	C/T	0.00279162	0.0372561	intron-variant	TOM1L2	GRCh38.p7	17:17951032	GATGTCTCCAGGGAT[C/T]TACCTGGAGCCAACC	146691
rs147559989	snp	C/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17864674	ACACCACCATGCCCA[C/G]CTGATTTTTGTATTT	146691
rs147642961	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17870785	TACCATTTATCCACT[C/T]AAGGATGCCCTCAAG	146691
rs147647643	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17954193	GCCAAAGGCCATGCT[A/G]AGCACAGAAAAGGAG	146691
rs147657261	snp	A/G	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17929826	CCCTGGCCTCAGTCA[A/G]ATACCACTTCTGCCC	146691
rs147665992	snp	C/G	0.00636936	0.0560724	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17845048	CAGATGGTGGGGTCT[C/G]GGAGCAGAGATCTCA	146691
rs147747231	snp	A/C	0.0138799	0.0821421	intron-variant	TOM1L2	GRCh38.p7	17:17849325	AAGACGCTGTTGACA[A/C]CAATAGCTGGAAACC	146691
rs147751619	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17934752	AAAGGCAAATAAGAA[C/T]GGCATCCAAAGCAAG	146691
rs147768977	snp	A/G	0.0209421	0.100162	intron-variant	TOM1L2	GRCh38.p7	17:17909009	ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA	146691
rs147850951	snp	C/T	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17915591	TAGCAGCATAGCTCA[C/T]TGCAACCTTGAAATC	146691
rs147873590	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17886873	CCAAGTTGGGCCAAT[C/G]AGATGCTCCTCCTTC	146691
rs147947479	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17844598	ACGCTGGTAAGCGAG[C/G]CAGTCATTCTCTCAG	146691
rs147956954	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17891833	TGTCAGAGGGAGACA[A/G]AGAGACAGAAGGATA	146691
rs148054363	snp	C/G	0.00318978	0.0398085	intron-variant	TOM1L2	GRCh38.p7	17:17970764	ATAGGCTCCACTAAA[C/G]GCTGGAAAGTAAGCT	146691
rs148099819	snp	A/G	0.0119091	0.0762411	intron-variant	TOM1L2	GRCh38.p7	17:17873190	TTTCCCCACTCCAGT[A/G]TTTTGTCATAAAAAT	146691
rs148118677	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17888580	CAGAATCTGGCCAGA[G/T]CCCAGCTACCAGGCT	146691
rs148129200	snp	A/G	0.00557542	0.0525036	intron-variant	TOM1L2	GRCh38.p7	17:17904496	AGGGTTGAAGAGCTC[A/G]AAGTGGAGCTGCCGA	146691
rs148152734	snp	A/C	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17951433	GGGTAGACACTGTAG[A/C]TTCTCAAGCCTCATG	146691
rs148181569	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17942908	ACATGAAGACTGTTA[A/G]AAGTAAACAAAAAGC	146691
rs148191024	snp	A/G	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17856721	AGCTCAGGCTCCATC[A/G]CATGTACCACAGCTT	146691
rs148268063	snp	A/T	0.00676609	0.0577691	intron-variant	TOM1L2	GRCh38.p7	17:17927212	AACTGCATTCTTCAA[A/T]GGGGGTGGAGTCCAA	146691
rs148310920	snp	G/T	0.00318978	0.0398085	intron-variant	TOM1L2	GRCh38.p7	17:17917018	TACATAAATTAGCTG[G/T]GCGCAGGGGCACACA	146691
rs148312891	in-del	-/AAAT	0.0973687	0.197999	intron-variant	TOM1L2	GRCh38.p7	17:17902179	AAAACTCCACCTCAA[-/AAAT]AAATAAATAAATAAA	146691
rs148321382	snp	A/G	0.00438332	0.0466095	intron-variant	TOM1L2	GRCh38.p7	17:17965579	CTTGCTGAGGGCAGC[A/G]CAGCGTGACAGGATA	146691
rs148329645	snp	C/G	0.0023933	0.0345097	intron-variant	TOM1L2	GRCh38.p7	17:17930916	CATTCCTCTAGGATG[C/G]GGATTTTTTTTCCCT	146691
rs148331137	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17845846	AGCAGAAGGCCCAGG[A/C]AGGTGTGGCATGTGC	146691
rs148341150	snp	G/T	0.00318978	0.0398085	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17861862	CTGAATGTCCAAAGT[G/T]CCCTAATACTCCTCA	146691
rs148363552	snp	A/T	0.0209421	0.100162	intron-variant	TOM1L2	GRCh38.p7	17:17911663	TTTTTTTTTTAATTT[A/T]TTTATTTTTTATTGA	146691
rs148412933	snp	C/G	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17875386	TGGTGTCATCACAGC[C/G]AGACCCTCAGCAGGC	146691
rs148425871	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17890501	ACAGTACCCCCAAAC[A/T]GCAAACACCAAGTCC	146691
rs148447343	snp	A/G	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17906994	AAGTCCACTCATGCC[A/G]CTTTCCCACTCCCGG	146691
rs148458682	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17953786	AACACAGGTAAAAAT[C/G]CCATCTCACAAAGTC	146691
rs148462085	snp	A/G	0.000153988	0.00877328	missense, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17882845	GCATGGTCGCAGCTG[A/G]ATCCACTTCAGGGAC	146691
rs148500340	snp	C/T	0.0115144	0.0749975	intron-variant	TOM1L2	GRCh38.p7	17:17944334	GCAGCCTTGCTGCGG[C/T]GCCCTTCATGAGTCT	146691
rs148502512	in-del	-/A/AA	0.391954	0.205789	intron-variant	TOM1L2	GRCh38.p7	17:17928156	AATTTTCTGTAACAA[-/A/AA]CAAAAAAAATCAGTA	146691
rs148581631	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17896152	TAGTGATCCATGGGG[G/T]CACTGAAATGAACCA	146691
rs148614635	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17919053	GAGAAATGTGCATTA[C/T]AATGGAGTCTAGAAC	146691
rs148632373	snp	C/T	0.00636936	0.0560724	intron-variant	TOM1L2	GRCh38.p7	17:17933594	AGGTTCTGATGCCCC[C/T]TAAGCATCATTTTGA	146691
rs148641956	snp	C/T	0.0260105	0.111035	intron-variant	TOM1L2	GRCh38.p7	17:17848321	AGGAGGACAGGAGCA[C/T]GGAGAGGCAGATGGA	146691
rs148693597	snp	A/G	0.000659076	0.0181412	synonymous-codon, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17850923	CCACACCTCAATGTC[A/G]TCCATGACAGATGGC	146691
rs148793622	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17853012	ACAGATGTGTTAACA[A/G]TGCCTAAGGCTGGCA	146691
rs148859609	snp	A/G	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17951212	AATGACCAGCACCCA[A/G]TAGACGGCAGTTCCC	146691
rs148902613	snp	A/G	0.0023933	0.0345097	intron-variant	TOM1L2	GRCh38.p7	17:17897405	AAAAAATCCAAACAG[A/G]TTCTCTGCTTTAAAA	146691
rs148953641	snp	A/G	0.00835141	0.0640778	intron-variant	TOM1L2	GRCh38.p7	17:17936453	AGAAACTTAAAAACA[A/G]GCATACCCTTTGACA	146691
rs148954790	in-del	-/CT	0.0146672	0.084371	intron-variant	TOM1L2	GRCh38.p7	17:17966356	AATTCTAAATAATCA[-/CT]CTTTTAGCCTGTCCA	146691
rs148972599	snp	A/G	0.02016	0.0983543	intron-variant	TOM1L2	GRCh38.p7	17:17865964	TCAGGCTGGTCTCAA[A/G]CTCCTGACCTCAGGT	146691
rs148983790	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17882924	ATAGCTGGACCTGGT[A/G]CCTACCCCACCCCAT	146691
rs149006338	snp	A/T	0.0023933	0.0345097	intron-variant	TOM1L2	GRCh38.p7	17:17929461	ACGTGGAGAAACCCC[A/T]TCTCTACTAAAAATA	146691
rs149026437	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17870814	AGCCCCGCACTGAGC[C/T]ACACACAGTGAAAAA	146691
rs149068874	snp	C/T	0.00636936	0.0560724	intron-variant	TOM1L2	GRCh38.p7	17:17910723	TACAGGCACGTGCCA[C/T]CATGCCTGGCTAATT	146691
rs149144863	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17965315	CAATCAGGCCTTATC[C/T]TCCCTTCCCAGTCTC	146691
rs149148558	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17845574	GCAGTGCTGAGGCTG[C/T]GGAGCACTGACTGCC	146691
rs149158661	snp	A/G	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17892364	CCCAGCCCTAGGTTT[A/G]TCTCTCCTCTTGGCT	146691
rs149193123	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17898110	TTTGTATTTTTAGTA[A/G]AGACTGGGTTTCACT	146691
rs149193716	snp	C/T	0.00636936	0.0560724	intron-variant	TOM1L2	GRCh38.p7	17:17925218	TCAGGTATTTCTTTA[C/T]GGCAATGCAAGAACA	146691
rs149197235	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17955941	TTGTTCGCTCCTACC[A/G]CCTGGAATTGTTCAT	146691
rs149218000	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	TOM1L2, DRC3	GRCh38.p7	17:17973874	CTGGATCTGTTATCT[C/G]TGAGGAGGCCACTCC	146691
rs149250807	snp	G/T	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17889694	TACTTTTCCATAATG[G/T]AAAGGTTAAGGCTGT	146691
rs149260887	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17938397	TTTGATTTCACTGCA[A/G]TGGCCTGAAGCTGCC	146691
rs149335483	snp	C/T	1.64789e-05	0.0028704	missense, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17882800	AGGAATAGGAACCAG[C/T]ACTTGTCCTCTGCTG	146691
rs149341172	snp	C/T	0.00279162	0.0372561	intron-variant	TOM1L2	GRCh38.p7	17:17872102	GCCAATGGACACTCA[C/T]AGGTCAAAACCCAGT	146691
rs149351273	snp	G/T	0.00636936	0.0560724	intron-variant	TOM1L2	GRCh38.p7	17:17922531	GCTCAGTGAGAAAAG[G/T]AGACAGGACAGCATG	146691
rs149419397	snp	C/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17943877	GCCCAAGGTCTAGCT[C/G]CCACAAACATACAGG	146691
rs149429221	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17858711	CCTCAGCCTCCCAAG[C/T]AGCTGGGATTACAAG	146691
rs149458835	snp	C/T	0.00279162	0.0372561	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847579	GTGGCCAGTGCCCGG[C/T]GTCCACGGGGTGCGA	146691
rs149516604	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17926524	AACATAGAAAGGTCA[C/T]GAATATCAACAGTGA	146691
rs149600136	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17953275	ACAGAGCGAGACTCT[A/G]TCTCAAAAAAATATA	146691
rs149637738	snp	C/T	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17900620	ATCACCTGTTTCCCA[C/T]TCCCAGCTTGACATA	146691
rs149647702	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17948979	AAAAAGTTAAGAGTG[C/T]CAAGCAGGGGTCAAA	146691
rs149786379	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17896828	ATATTAACAATTTTG[A/G]TGGGTACAGATATGA	146691
rs149795232	snp	A/C	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17864257	GCTCTGTCACCCAGG[A/C]TGGAGTGTAGTAGAG	146691
rs149805330	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17914422	CCCTCCCTTGGGGGG[C/T]TCTGATTTCCCTGTT	146691
rs149829211	snp	A/G	0.00993419	0.0697739	intron-variant	TOM1L2	GRCh38.p7	17:17929076	CACTGCTGTGAGAAC[A/G]GGCCTTTCCTTGGCT	146691
rs149849266	in-del	-/AAAAAAAAC			intron-variant	TOM1L2	GRCh38.p7	17:17928057	ATGGATGAACCAAAA[-/AAAAAAAAC]CTGCCATGAATTGAT	146691
rs149873726	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17966923	TTTGCAAATTCCTGC[C/T]CTTGAACATCAGACT	146691
rs149918611	in-del	-/TC	0.0759472	0.179459	intron-variant	TOM1L2	GRCh38.p7	17:17871199	TACGGTGAAACCCCG[-/TC]TCTACTAAAAACACA	146691
rs149968726	snp	A/T	0.00279162	0.0372561	intron-variant	TOM1L2	GRCh38.p7	17:17950857	CCCAGGAGAATGGAA[A/T]CTGCAAGATCTGGGA	146691
rs149987323	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17891873	CAGAACAGGGACGAG[A/G]GACAACCCTAGGGTA	146691
rs149996996	snp	C/G	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17940882	CCCAAGAAAGCCAGA[C/G]TGTCATTCGAGCAAT	146691
rs150017352	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17869782	GATTGCTTTTTCTCA[A/G]CAAAATATTCCAGAC	146691
rs150032341	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	TOM1L2, DRC3	GRCh38.p7	17:17972877	AGGATGTCTCCCTTC[A/T]GACTTCCCCTTAGCA	146691
rs150069096	snp	C/T	1.64863e-05	0.00287104	synonymous-codon, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17907491	GATCTCCATATTCAA[C/T]GTCCAATCCTCACTT	146691
rs150087002	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17937998	TGATGTCCACACAAA[A/G]GCTTGACTGGGATTT	146691
rs150125461	snp	A/G	0.00318978	0.0398085	intron-variant	TOM1L2	GRCh38.p7	17:17916365	GGCATGAATCACCGC[A/G]CCCGGCCTATTTTAA	146691
rs150133962	snp	C/T	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17931232	CTATCCTCTTTAAAT[C/T]CTTCCTCTTCTACAG	146691
rs150156162	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17860225	CTGGGCTCTCTAATG[C/T]CCACGCTGGGGCAGG	146691
rs150281431	snp	A/C	0.00398564	0.0444627	intron-variant	TOM1L2	GRCh38.p7	17:17921465	GTACTTAATGGAATA[A/C]CTTACGTGTGAGTCA	146691
rs150292198	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17894534	CACCACTTTCTCCCT[A/G]AATGGCCCAGGACAG	146691
rs150315008	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17943070	GATTGGCCAGATGCT[C/T]AGAAGCTGAGTCATG	146691
rs150345845	snp	G/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17889378	AGAAGGTGGGCTGGG[G/T]GCAGGCAGATATGCA	146691
rs150404032	snp	C/T	0.000181277	0.00951871	synonymous-codon, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17882780	GTAGGGAGCAGGAGG[C/T]GGCGAGGAATAGGAA	146691
rs150439624	snp	C/G	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17883937	TTTCCTGGCTCTCCC[C/G]CAGGCTAGGAGTGGA	146691
rs150454237	in-del	-/T	0.0314385	0.121371	intron-variant	TOM1L2	GRCh38.p7	17:17906053	ATAATCCTCACCCCC[-/T]ACTCCCTCATCTCCT	146691
rs150494085	snp	A/C	0.0244538	0.107838	intron-variant	TOM1L2	GRCh38.p7	17:17877899	AAAAAAAAATCCCAA[A/C]CCCCCTCTCCCCCCA	146691
rs150561338	in-del	-/T			intron-variant	TOM1L2	GRCh38.p7	17:17928796	GTCTGTGTCTCAGGA[-/T]TTTTTTTTTTCTTTA	146691
rs150590314	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17923667	TGCACTCCAGCCTGG[C/G]CAAGAGGGTGAGACC	146691
rs150631349	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17913768	CCCTTCCCCAGTATC[A/G]TAAGAGGAAAGGAAA	146691
rs150642526	snp	C/G	0.00636936	0.0560724	intron-variant	TOM1L2	GRCh38.p7	17:17957965	CGTGGTGGTGGGCGC[C/G]TGTAGTCCTAGCTAT	146691
rs150666718	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17891663	GACATGCTTTGTGAG[A/G]AGAAGCCACCATTTG	146691
rs150684003	snp	C/T	0.0178098	0.0926698	intron-variant	TOM1L2	GRCh38.p7	17:17905124	TTAGAGATGTGTAGT[C/T]CCTAACAACTATTTG	146691
rs150746086	snp	C/T	0.0023933	0.0345097	intron-variant	TOM1L2	GRCh38.p7	17:17885393	GGGAAGAAGAGCCCA[C/T]TGGGAGCTAGACCCA	146691
rs150784633	snp	C/T	8.24219e-05	0.00641905	missense, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17850946	CAGATGGCTGCGCAA[C/T]GGGGATCTATGGAGG	146691
rs150799747	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17880504	TCCCTCAACCCCCTC[A/G]AAGGATCTGCAGAAA	146691
rs150803663	snp	A/T	0.00478085	0.0486577	intron-variant	TOM1L2	GRCh38.p7	17:17966166	AACCCAAAAGCCTTT[A/T]GCTATTATTATTACC	146691
rs150875750	snp	C/T	0.00318978	0.0398085	intron-variant	TOM1L2	GRCh38.p7	17:17933842	ATTGGCTTATTTTTT[C/T]AATCAAATCCATCCT	146691
rs150895229	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17947423	TCACAATATGACTGA[C/T]TGAATTTGGAGACAG	146691
rs150897719	snp	C/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17862332	CACTTATTTTAGTCA[C/G]GAAAATCTCGCTGTA	146691
rs150960424	snp	C/T	0.00358779	0.0422022	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17844044	CCCAAGTGGGTGAGA[C/T]GTCCCCAAAGCCGAC	146691
rs150961477	snp	A/G	0.0777841	0.181223	intron-variant	TOM1L2	GRCh38.p7	17:17962757	CAAGGTCAAGAGATC[A/G]AGACCAACCTGGCCA	146691
rs150992296	snp	C/T	0.00398564	0.0444627	intron-variant	TOM1L2	GRCh38.p7	17:17908548	ATATATGATAAGGGG[C/T]TAATATCCAGACTAC	146691
rs151035387	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17896295	AAGTATGCTTTATTT[C/T]GTGAGAAGCAGGTGG	146691
rs151099170	snp	A/G	6.59881e-05	0.00574367	synonymous-codon, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17879717	GTTTCCTCGAACGAC[A/G]TCCAGTTCACTCCGC	146691
rs151123049	snp	A/G	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17883312	TGCAATTTACCAAAT[A/G]TTTTTTGTAATTATA	146691
rs151150802	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17954993	GTTGCTCACCCTAGA[A/G]CAATGTCTTTATGTT	146691
rs151152770	snp	A/G	0.021333	0.101051	intron-variant	TOM1L2	GRCh38.p7	17:17871137	AAACTATTGGAGGCC[A/G]AGGCGGATGGATCAC	146691
rs151155378	snp	A/T	1.64727e-05	0.00286986	missense, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17884717	TCAGCTCCTCATATA[A/T]GTGCACAACGCCGGT	146691
rs151184467	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17936695	TATAAGCTGTTTTTT[A/C]ATTAAAAATGATTAT	146691
rs151202379	snp	C/T	0.00358779	0.0422022	intron-variant	TOM1L2	GRCh38.p7	17:17950507	CTATCTTACCAAGGC[C/T]GGCCTCAAGCTCCTG	146691
rs151244996	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17940361	CAATAAATACTATTA[A/G]AATCATTTTACAGAT	146691
rs151248056	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17853301	TACACCTGACCAGCT[C/T]TTGTCCACTTAGCAG	146691
rs151331597	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17926076	CTCCACAGGCTGAGG[C/T]GAGAGGATCACTTGA	146691
rs180793648	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17863123	AAGGCAGGGACTGGC[A/G]CCAGTGCACCTGCAG	146691
rs180817975	snp	C/T	0.00358779	0.0422022	intron-variant	TOM1L2	GRCh38.p7	17:17899993	AAGGCAGGTGGATAA[C/T]CTGAGGACAGGAGTT	146691
rs180839283	snp	G/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17940695	TCCTAATTAAAGGCT[G/T]GTCTCCACAGCTGTC	146691
rs180843327	snp	C/T	0.00676609	0.0577691	intron-variant	TOM1L2	GRCh38.p7	17:17851442	GGGCAGCACCAGCCC[C/T]GGGGGGATGCAGGGG	146691
rs180882891	snp	C/T	0.00438332	0.0466095	intron-variant	TOM1L2	GRCh38.p7	17:17919662	GGGGAGGAGGGGCCA[C/T]GGTGTTGTTGCAAGT	146691
rs180892119	snp	A/G	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17876674	GATCACTCCAGTCTA[A/G]AGAGGAGAAGGGGGC	146691
rs180931090	snp	A/G	0.00318978	0.0398085	intron-variant	TOM1L2	GRCh38.p7	17:17855573	CCATTGACAAGTCTC[A/G]TTTCTCTTCAACCAG	146691
rs180964056	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17938117	CCCAGCGTGGTGCAA[C/T]GGGAAGAGGAGAGGA	146691
rs180986569	snp	A/C	0.00478085	0.0486577	intron-variant	TOM1L2	GRCh38.p7	17:17882378	GCATCTCTGCATTTA[A/C]ATGTCATTGCTGAGC	146691
rs180994680	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17903916	GGTCAGAGGCCTTCA[C/G]GGAGGGCACAAAGGG	146691
rs181001709	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17925517	TAATGACCAAAACTA[A/T]AAGCCAGTTATTTAA	146691
rs181008987	snp	A/C	0.00795532	0.062565	intron-variant	TOM1L2	GRCh38.p7	17:17956660	ACCGCTGAGACCCGG[A/C]GAGAATTCCAGCACA	146691
rs181021970	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17944781	GGGAAACAGGAGGTC[C/T]GCACTTGTGCTCTCC	146691
rs181026118	snp	A/C			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17844565	CCCCTTGAGGCTCCA[A/C]AGCTCCTTGTCCCAT	146691
rs181032615	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17964267	GACTACTAGGTTAGC[A/G]CAACATTTCTGGGTG	146691
rs181040846	snp	C/G	0.00398564	0.0444627	intron-variant	TOM1L2	GRCh38.p7	17:17870459	TGCCAGGCTGGCCCC[C/G]AAGCATGTGACCAAA	146691
rs181043608	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17894558	AGGACAGATCTTTCT[G/T]AGCCTCAGCATCCTC	146691
rs181064706	snp	C/G	0.00597247	0.0543191	intron-variant	TOM1L2	GRCh38.p7	17:17956481	AGCTGCCTGCCAGTC[C/G]CTGGCAGTGCGCCTG	146691
rs181072832	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17936926	AACAGTCTAAGTTCA[A/G]CCTCTTTGATTCTTC	146691
rs181090156	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17916038	ATATCTCAGAAATCT[C/T]TGCTAAATCCAATGT	146691
rs181114038	snp	A/G	0.0023933	0.0345097	intron-variant	TOM1L2	GRCh38.p7	17:17944506	ATGATCCGTGGGATC[A/G]GAGATTTGGTGTCTT	146691
rs181125450	snp	A/G	0.0134861	0.0810011	intron-variant	TOM1L2	GRCh38.p7	17:17924086	AGGTTGCAGTGAGCC[A/G]AGATCGCGCCACTGC	146691
rs181129601	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17854831	GAGCCACTGCACCCA[C/G]CCTGACATGCCATAG	146691
rs181138363	snp	C/T	0.00517822	0.0506191	intron-variant	TOM1L2	GRCh38.p7	17:17881278	GGCTATGGGCAGCCA[C/T]CCAGTAGACTCTGAA	146691
rs181220441	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17959478	AATACCACTAAGACC[C/T]TTTCAACTAGAGTCT	146691
rs181471332	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17844106	GTGCCAGAGGCTGAA[A/G]CCAGGCTGCAAGCAA	146691
rs181559941	snp	A/G	0.00279162	0.0372561	intron-variant	TOM1L2	GRCh38.p7	17:17883204	AAGTGGAGGGAGGGC[A/G]GTTATTAAGTTTTGC	146691
rs181575621	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17905125	TAGAGATGTGTAGTC[C/T]CTAACAACTATTTGT	146691
rs181581388	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17926814	AGTGAGCAAGGATCA[C/T]ACCACTGCACTCCTG	146691
rs181590691	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17875545	CAGGAATTTCCTAAA[C/T]GCTGACGACTTCAGC	146691
rs181599107	snp	C/T	0.00279162	0.0372561	intron-variant	TOM1L2	GRCh38.p7	17:17899828	CAGTTTTAAAACATT[C/T]ATACTCTACCAAATG	146691
rs181628481	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17939907	GTTAAGAATTCTGCT[A/T]TGGGCCAGGTGTGGT	146691
rs181634161	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17919006	GCTCGGTTCCCAGCT[A/G]TCCCCGGTTCTCCCT	146691
rs181658867	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17959411	GTCATACATCACAGA[C/T]ACCCTCTCTGGCCTT	146691
rs181717141	snp	C/T	0.0150606	0.0854603	intron-variant	TOM1L2	GRCh38.p7	17:17936167	CTCTGGCCTTAGCTC[C/T]CCCAGGCGTGTGCCC	146691
rs181717552	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17893414	CCACCCTACCTGCCT[C/T]TGTGAGCAGCAGAGG	146691
rs181720210	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17856207	CTGGATCTTCCCAAT[C/G]AATGGACATGGTTTC	146691
rs181772552	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17888620	TCAAAGAACACACAC[C/T]TCCAGTTTCTCCTGT	146691
rs181777346	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17910755	TTGTATTTGTAGTAG[A/G]GATGGGTTTCGGCAC	146691
rs181780341	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17877263	ATCCTAGGGCTGACA[C/T]CACCAATTATCTCTC	146691
rs181810674	snp	G/T			upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	TOM1L2, DRC3	GRCh38.p7	17:17972943	AGACGCGTCTGCTGC[G/T]TGGAACCGCCGAGTT	146691
rs181820601	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17949208	TCTCCACCTTCATCT[C/T]TTCCCAGTGCTAGGT	146691
rs181825341	snp	C/G	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17929904	CACAACATGAATTTC[C/G]ACAACAGCAAGGCAG	146691
rs181851330	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17869545	ATCTCCTTTGAAAAA[A/C]TTTGTACTGATTCTT	146691
rs181852871	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17864274	GGAGTGTAGTAGAGC[A/G]ATGTCGGCTCACTGC	146691
rs181853250	snp	A/G	0.00279162	0.0372561	intron-variant	TOM1L2	GRCh38.p7	17:17955874	GGCTTCAAGAGTGAA[A/G]CTGCAGACCTTCGCG	146691
rs181856064	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17950835	AGGGAAAACCATGAA[A/G]GTAGTCCCCAGGAGA	146691
rs181867562	snp	G/T	0.0023933	0.0345097	intron-variant	TOM1L2	GRCh38.p7	17:17911086	CCAAACAGGGCTGCC[G/T]TAGGTTTCAGAGAAC	146691
rs181930679	snp	C/T	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17965400	CTACCTCTTAACATC[C/T]AGCATTTGCTCAAGT	146691
rs181936569	snp	A/C/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17945676	ACCTTAATATTTCAC[A/C/G]GAGACTTTCTCTGCA	146691
rs181963697	snp	G/T	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17921400	TAAAATGCATTTGGG[G/T]TGTGCTCTCTAGAAG	146691
rs181987485	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17959636	ATTTCGACTAATGAC[A/G]TGCCAGAAATCTGTG	146691
rs182112147	snp	A/G	0.0588605	0.161139	upstream-variant-2KB, intron-variant	TOM1L2, DRC3	GRCh38.p7	17:17973605	TTTATTCTTTTTTAA[A/G]AAAAATTTTGTTCAT	146691
rs182119577	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17889297	AGTTGGCCAGGGTGC[C/T]ACTGATGGCAAAGGT	146691
rs182122807	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17930547	CAGCAGCCTCTTGCA[A/G]TCAGCTCATCAATAT	146691
rs182169958	snp	A/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17864649	CCCTAGTAGTTGGGA[A/T]TACAGGCACACACCA	146691
rs182181044	snp	C/T	0.00636936	0.0560724	intron-variant	TOM1L2	GRCh38.p7	17:17889807	AAACCTTTGCTTCTC[C/T]AGTTAAACTGCAGGC	146691
rs182199340	snp	A/G	0.00398564	0.0444627	intron-variant	TOM1L2	GRCh38.p7	17:17863812	CCTCGGCCTCCCAAA[A/G]TGATGAGATTGCAAG	146691
rs182272066	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17900150	CCTGGGAGACGGAGG[A/T]TGCAGTGAGCTGAGA	146691
rs182282131	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17941355	GTGTCCTGGCTCTGC[C/T]CTCGGATGACTATGG	146691
rs182290751	snp	A/T	0.00159617	0.0282053	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17859537	GCTCTGCTGCCCTGT[A/T]TCGCTAAGGCTGTGG	146691
rs182295987	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17885882	GTGAGCTGAGATGGC[A/G]CCACTGCACTCCAGC	146691
rs182337909	snp	A/G	0.00636936	0.0560724	intron-variant	TOM1L2	GRCh38.p7	17:17927443	CTGAGGCCAGGACCT[A/G]CATGCAGACCTTTCT	146691
rs182343095	snp	A/C	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17907659	GCCAACAGAGCCATT[A/C]TAGGAGTGCTATTAT	146691
rs182530109	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17951917	CAAACAGTCACTCGG[A/G]CTCTGTTGGTGAGGG	146691
rs182537814	snp	C/T	0.00398564	0.0444627	intron-variant	TOM1L2	GRCh38.p7	17:17931642	TACACATGAGGGGAC[C/T]TCAAAAATGGAGTTG	146691
rs182539922	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17873769	TTCTCCCTGGGTAAA[A/G]TAAGGGGGCTGCATT	146691
rs182548301	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17912496	GCAGAGACACTCCTC[A/G]CCTCCCAGACGGGGT	146691
rs182550518	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17897696	CTATTTTCAGTTTTT[A/G]CCCCATGCAAAAGAC	146691
rs182575666	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17848713	TGGCTCAGGGCCTGG[C/T]ACCAGTAGGTGCTCT	146691
rs182598335	snp	C/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17957857	CTGTAATCCCAGGCC[C/G]AGGTGGGCGGATCAT	146691
rs182603238	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17938971	ACAGCAAGCAGTGGC[A/T]CCTGGACTAGAATTC	146691
rs182678645	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17916924	GCATTTTGGGAGGCC[A/G]AGGCAGGTGGATCAC	146691
rs182712491	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17871779	TCTTCACTCAGAGAA[C/T]GGGGAATTCTTGTTC	146691
rs182725246	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17946709	AACATCAGCTCATTA[C/T]ATTGGTCTAAGTATT	146691
rs182850026	snp	A/C	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17966531	CCCACCCCAAACCTA[A/C]TGAAACAGAAACTCT	146691
rs182853768	snp	C/T	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17883821	TAAGTCGTGTTCCTA[C/T]GAGAGATGTGCACAG	146691
rs182868069	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17927240	CAAAGGGACAGGCCC[A/G]ACATTATTTTCAGCA	146691
rs182949495	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17895085	GTTCAGAAGGCTGCT[A/G]TACACACGACGAAGG	146691
rs182987019	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17845207	GGTGCAAGCAGGCCA[C/T]CTGAGGGGTGGCTCC	146691
rs183006761	snp	C/G	0.00119737	0.0244387	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17846686	GCTGTTTGCTGCTGG[C/G]TCTTGAGGCAGATGT	146691
rs183019158	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17872675	ACACATGAGGACCGA[G/T]CCAGGCACTGCTGAG	146691
rs183034102	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17853443	GCTAAAGAACAAATC[C/T]CTTGAGGCCTGGGGT	146691
rs183043553	snp	A/C	0.00953873	0.0683987	intron-variant	TOM1L2	GRCh38.p7	17:17942766	AAGCAGTCACATCAG[A/C]ACGGTAGTTAGTATA	146691
rs183047943	snp	A/C	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17902056	TGGTACACACCTATA[A/C]TCCCAGCTACTCAGG	146691
rs183052911	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	TOM1L2, DRC3	GRCh38.p7	17:17974149	TGCCACGTGCTAAGT[A/G]TATGAAGTTGGGCAT	146691
rs183109465	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17913624	TCTGCAAAATGAAAA[G/T]AAAGAAGCATTCTTT	146691
rs183123479	snp	A/C/G	0.00914312	0.0669923	intron-variant	TOM1L2	GRCh38.p7	17:17877640	GCTGTGTCTGTTCAC[A/C/G]GCTGTCCACAGTGCT	146691
rs183134710	snp	A/C	0.00636936	0.0560724	intron-variant	TOM1L2	GRCh38.p7	17:17901643	TCTGTCACCCTGAAC[A/C]TGCCCTCCCCATTAT	146691
rs183141836	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17932465	CAGAAAACATACGTC[C/T]CTTTGTTTCCTGGGG	146691
rs183145072	snp	A/C/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17921801	CCTCTCGGCCTCTTC[A/C/G]TGCAGTCTGCTTTGC	146691
rs183149098	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17857398	GGTCAGATGCTTTGA[A/G]TCTGTTCCCTTAGAA	146691
rs183158250	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17946560	TTTCTTTCCCATCTC[A/G]ATTCTGATATATTTA	146691
rs183166875	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17852822	GTGAGCCGAGATCAC[A/G]CCATTGCACTCCACC	146691
rs183168143	snp	C/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17905857	GTTGCTCTGGTTCTA[C/G]ATGGCCCTGTGTTAT	146691
rs183171625	snp	A/G	0.00636936	0.0560724	intron-variant	TOM1L2	GRCh38.p7	17:17953752	AATCCTGTTGGTTGT[A/G]TGATTCTGAGAAAGT	146691
rs183176909	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17960546	TTTCGCCATGTTGCC[A/C]AGACTGGTCTCGAAC	146691
rs183183660	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17941694	GGCTCTGCCACATTT[A/G]TTATCTTCCAATGAT	146691
rs183219988	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17851799	ACTGGGGCGCAGCAG[C/T]CAGAGCCAGGGAGGT	146691
rs183239600	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17908497	AAGGACACAACACAG[C/T]GAACCTGCAGAGGAA	146691
rs183267086	snp	C/T	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17947573	TCTGAAGAAGCCAAA[C/T]CTGCAGCTTGATCTT	146691
rs183274248	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17928213	ACTTTGACCCGGCAA[C/T]AGCCCCCTAAGGAAA	146691
rs183297969	snp	G/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17961518	AGTTCGAGGCTGCAG[G/T]GAGCTATGATCATGC	146691
rs183305989	snp	A/G	0.00398564	0.0444627	intron-variant	TOM1L2	GRCh38.p7	17:17878612	AGCAGGGTAGAAGGT[A/G]TAGCACTTGGGGACC	146691
rs183313763	snp	C/G	0.00279162	0.0372561	intron-variant	TOM1L2	GRCh38.p7	17:17922339	AGGAGGCCAGCTCTG[C/G]AGTGTCCTTTCATTT	146691
rs183335306	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17968491	CCAAGGTAGTGAAAC[C/G]TTGTCTCTACTAAAA	146691
rs183563807	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17866772	TCTTCAATTTCCCAA[A/C]TATTTCAAAACCAGT	146691
rs183614612	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17948743	CCTTCAGTTCACACC[C/T]CCTCTTGCTAAGAGT	146691
rs183627778	snp	A/G	0.00398564	0.0444627	intron-variant	TOM1L2	GRCh38.p7	17:17914149	TCATTCCCTCTGGGC[A/G]TGGACAGAGGAGGGG	146691
rs183634824	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17954270	CGGGAAGAAGCCCAG[A/T]CAGTGAAGGCCTTGA	146691
rs183778523	snp	A/G	0.0166325	0.0896639	intron-variant	TOM1L2	GRCh38.p7	17:17961789	AGGCAGGAGAATGGC[A/G]TGAACCCGGGAGGTG	146691
rs183815207	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17932750	AAAATGGAGTTAATA[C/G]TATTAATAAATATGG	146691
rs183840182	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17891550	ACAGTGCAGTTCACA[A/C]CCCTTGTGATAACTG	146691
rs183875951	snp	C/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17938451	GACAACAGTCCCGCT[C/G]TGACTAGGATGTTCT	146691
rs183891231	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17899904	GGTTGATGCTCTGCT[A/G]ATCAGCTTAATTTAA	146691
rs183916309	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17940149	AGTGAGCTGAGATCA[C/T]GCCTCTGCATTCCAG	146691
rs183919769	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17895977	CACCTTAGGAGGCCC[C/T]GGGTTCCTCTGGGCT	146691
rs183923402	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17919267	TACAGAGGACCTTTC[C/T]TTGCTGTTACTTCTA	146691
rs183935738	snp	C/T	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17875626	ACTTGTACAAAAGCC[C/T]TCCAACTATTAGAAC	146691
rs183935994	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17887873	GAATTCAGTTCTCAC[A/T]GTTACTAAGCATCCT	146691
rs183944886	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17909861	TAGCAAGACATTGTT[C/T]CTACAAAAAATTTAA	146691
rs183945118	snp	C/T	0.00438332	0.0466095	intron-variant	TOM1L2	GRCh38.p7	17:17865727	GTTCCATATAAAACA[C/T]GGCAGGTGACCTTTC	146691
rs183954004	snp	A/C/G			intron-variant	TOM1L2	GRCh38.p7	17:17929319	GCAGGCTTTGGGTGG[A/C/G]TGAGAGGGGTTGATA	146691
rs183959980	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17958336	TTGGTTTCTCTGGTC[C/T]GGACCAGTGCCAGAA	146691
rs183966880	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17959423	AGACACCCTCTCTGG[C/T]CTTGTTTCCACAACC	146691
rs183967319	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17863170	TTCTCGCTTGGGCTC[C/T]TCATTAACTCAATCA	146691
rs184092221	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17917201	GCTGGGCGTGGTGGC[A/G]CACACCTGTTGTCCC	146691
rs184093720	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17957012	CAACGGCTGCCAGCA[C/T]GCTGTCACCTCTCAA	146691
rs184179818	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17867963	TCAAAGACACTCTAA[C/G]CAGGATAGCACTTCC	146691
rs184183837	snp	G/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17892410	CTTGCCTCTGCCACA[G/T]CACTAATCACCCAGG	146691
rs184187648	snp	A/G	0.00358779	0.0422022	intron-variant	TOM1L2	GRCh38.p7	17:17962534	GCGCAGGCTGGTCTC[A/G]AACTCCTGAGCTCAG	146691
rs184191454	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17914636	GCTTCTGTAACTGCC[A/G]GCCTGGTGCCATCTG	146691
rs184233255	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17954878	AAAACTCTCACACAG[A/G]TACTACGCTCTAAGG	146691
rs184259774	snp	A/C	0.00318978	0.0398085	intron-variant, upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17971503	AGTCCCTCCTACAGC[A/C]CAGCTGAGTTGCAGC	146691
rs184467300	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17903349	GAGTAATTGGCTGGG[C/T]GCGGTGGCTCACGCC	146691
rs184494388	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17943856	GGCCCCACGTGAACA[C/T]CCAGAGCCCAAGGTC	146691
rs184501752	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17918045	TTCAGCAACGTTTTA[C/T]AGTTTTCGGTGCACA	146691
rs184503682	snp	A/C/T	0.0023933	0.0345097	intron-variant	TOM1L2	GRCh38.p7	17:17923098	CATACCTGCTGTGCT[A/C/T]ATTAAAGCCACAGTG	146691
rs184511473	snp	C/T	0.00597247	0.0543191	intron-variant	TOM1L2	GRCh38.p7	17:17879984	TCTCTGACTGTGACA[C/T]GAAAGCAGTACCACG	146691
rs184532928	snp	A/G	0.00597247	0.0543191	intron-variant	TOM1L2	GRCh38.p7	17:17874244	CAGGCGTGAGCCACC[A/G]CGCCCAGCCATTACT	146691
rs184565189	snp	A/G	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17854411	CCCTTAGGAGGCCTC[A/G]GTATCCTCATCTGTC	146691
rs184576586	snp	C/T	0.00398564	0.0444627	intron-variant	TOM1L2	GRCh38.p7	17:17878984	ACTGCAGGCCGCCCA[C/T]TCCTGGACCCCATTC	146691
rs184585913	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17903137	CCACTGCCACTGCAC[C/T]AGTCTCCGTAGCTAT	146691
rs184602373	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17850038	GCCCACAGACAGCCA[A/G]GCTGACCCTGTGGTT	146691
rs184627904	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17922759	CGCAATAAATATGAA[C/T]CACAATTCTTAACTT	146691
rs184652533	snp	A/G	0.00398564	0.0444627	intron-variant	TOM1L2	GRCh38.p7	17:17928928	TTATGAAGCCAGCAA[A/G]GCAAAACAAAATCAA	146691
rs184673889	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17939653	TGTAGAAGTTCATTA[C/T]ACTATTCTACTTTTG	146691
rs184674027	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17898216	GGTGTGAGTCACCGC[A/G]CCTGGCCAACATTTT	146691
rs184690664	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17971150	CTCTACATTGCCAAC[A/G]AAAGATTTCAGCTTT	146691
rs184710098	snp	A/G	0.00146621	0.0270362	intron-variant	TOM1L2	GRCh38.p7	17:17850852	AGAAGAGCCTCTGCC[A/G]CTCCACACCCCACAG	146691
rs184721103	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17874893	GGCTTCCACATCAGG[G/T]ATTTCCAGGGGTCTC	146691
rs184747207	snp	C/G/T	9.88643e-05	0.00703024	synonymous-codon, upstream-variant-2KB, intron-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17862763	CAAGGAGTTTCCTCT[C/G/T]GTCTGGGCAAACATG	146691
rs184787643	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17854908	GGGATCTGAAGAAGC[A/G]TATGAGTTGGAAGAG	146691
rs184821419	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17909347	AAAAGGTGTAAACAG[A/C]CTGTGTCCATCAATT	146691
rs184837957	snp	A/T	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17948162	CTTAGTCAAATAGTT[A/T]CATTTTGAAAGACCA	146691
rs184851169	snp	C/G	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17955235	CTTCTATCATACTCA[C/G]CAGACAATATGGTGG	146691
rs184874285	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17944611	TGGAGTTATTCTCCC[C/T]AAAGCACCAGGCACC	146691
rs184884476	snp	C/T	0.0154538	0.0865337	intron-variant	TOM1L2	GRCh38.p7	17:17912674	AGGTGGGATGGCGGC[C/T]GGACGGAGACGCTCC	146691
rs184907863	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17951925	CACTCGGGCTCTGTT[A/G]GTGAGGGGCTCATTT	146691
rs184908441	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17881555	TGCCCATAGAAGCAG[A/G]GCCAAAAGCCAGAGA	146691
rs184916121	snp	C/T	0.00279162	0.0372561	intron-variant	TOM1L2	GRCh38.p7	17:17864895	GTGGCTACAAATATA[C/T]GAAATATTGAGAAGC	146691
rs184918487	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17931827	ACACTGACTTCCTAT[C/T]TCACACAATAAAGAT	146691
rs184926314	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17890203	CTCCATGCTCTAATG[A/G]AGAAGATTGAAAACA	146691
rs184943066	snp	A/G	0.00914312	0.0669923	intron-variant	TOM1L2	GRCh38.p7	17:17924469	GCTGTTGAAAAATGG[A/G]AGAAAAGCTACTAGG	146691
rs184971919	snp	A/C	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17963037	AAATAGAAACAGGTG[A/C]CCTCATGGAACATTT	146691
rs184978945	snp	C/G	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17956100	AGAACAAAGCCTCCC[C/G]CGCACGAAAAAGGAC	146691
rs185377366	snp	C/T	0.0162398	0.0886349	intron-variant	TOM1L2	GRCh38.p7	17:17864314	CTCCCGGGTTCACGC[C/T]ATTCTCCTGCCTCAG	146691
rs185431675	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17843987	CAGACAATGTCTCTG[A/G]GGTGGAAACACTTCT	146691
rs185469975	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17854536	ATTTAATTAATTAAT[C/T]TATTTAGAGACAGAG	146691
rs185496957	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17892780	TCTAACAAATAGAAT[A/G]TAACAGAAAAAAATG	146691
rs185503737	snp	C/G/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17935403	ACTCCTTGATTTAAA[C/G/T]TGGGCTTGCTGCATT	146691
rs185528496	snp	C/T	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17916401	TTATAGTTTTCCCTT[C/T]GCTCTTATGTTTAGG	146691
rs185548860	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17844972	TGGGCCTTGAGAGTC[C/T]AGGTTTCCTGACAGA	146691
rs185549052	snp	C/T	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17956515	TCCTCAGCCCTTGGG[C/T]GGTCGATGGGACCGG	146691
rs185554916	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17938078	ACCAAGAGCAGAGAC[C/G]TCCCTCTGTGTTACT	146691
rs185560860	snp	A/G	0.0023933	0.0345097	intron-variant	TOM1L2	GRCh38.p7	17:17870929	GTATCCTGCAACACA[A/G]CACTCACACAGGGGC	146691
rs185571786	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17894790	ACAAAAACTAGCCAG[A/G]CTTGGTGGCACATGC	146691
rs185593838	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17861702	GACATTGAGCAGAGG[C/T]TAAGGGCTCATGTTG	146691
rs185594787	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17943077	CAGATGCTTAGAAGC[C/T]GAGTCATGGGTACAC	146691
rs185614934	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17939830	ATAAACACATTTGTT[A/G]AGTCCCCATTATGTA	146691
rs185618648	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17868942	AGAGGAAATCCTTTT[C/T]CTTACTAGAGATTTT	146691
rs185634819	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17915384	TACCAGGTGTGAAGT[A/G]GTATCCCAGTGTGGT	146691
rs185731377	snp	C/T	0.00517822	0.0506191	intron-variant	TOM1L2	GRCh38.p7	17:17886442	GGAGAGTAGGTTGCC[C/T]GTAGGGAGTGCCTCT	146691
rs185737836	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17959256	GGGGCAGTCTTGTGG[A/G]ACTGAGCCCTTAACC	146691
rs185758132	snp	C/T	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17918547	GCAAGAGGGTGAAAA[C/T]AGGAACCATAACAGG	146691
rs185765198	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17919864	CTACCATCCCACGCC[A/C]CAGCCGCCAGGAAGG	146691
rs185795088	snp	G/T	0.00517822	0.0506191	intron-variant	TOM1L2	GRCh38.p7	17:17959514	TTCTTTGAATTGCTG[G/T]TTTAAGAATTTCCAC	146691
rs185886306	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17941108	TTCTCCAGTGAACAG[A/G]TGGAAGGGTCATCTC	146691
rs185915613	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17900041	ACATGGTGAAACCCC[A/G]TCTTTACTGAAATAT	146691
rs185923997	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17966010	CCTGTAATCCCAGCT[A/G]CTTGGGAGGCTGAGA	146691
rs185936983	snp	C/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17945837	TAAGTCTGCCACCAC[C/G]CTAATTCAATCTTTT	146691
rs185946084	snp	A/C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17926836	GCACTCCTGTCTGGG[A/C/T]GACAGAGAGGGACTC	146691
rs186015839	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17844128	TGCAAGCAAGTGCTC[A/C]TCCACACTGCTCTTC	146691
rs186024126	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17869988	CTTCCATAGGACAGG[C/T]TCCTTAGCAGGGAAA	146691
rs186028319	snp	A/C	0.00113351	0.0237796	intron-variant	TOM1L2	GRCh38.p7	17:17893632	CATCTTACTCTGTTC[A/C]AACAAATTGGGCAAG	146691
rs186123000	snp	C/T	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17876987	GGATTTGACGCATAG[C/T]TCAAGAGGAGGAGTT	146691
rs186250583	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17851470	GGGGTCTGTTTGCTC[C/T]GCTGAAGAGATTTTG	146691
rs186271076	snp	C/T	0.00953873	0.0683987	intron-variant	TOM1L2	GRCh38.p7	17:17889579	GGGTTCTACCTCTGC[C/T]AGGACCCCCAACCAT	146691
rs186289448	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17851212	GAAGGTGGCTGTACG[C/T]GTTCTTGAAATGGAG	146691
rs186319060	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17930630	CCCTTTATTAACTTT[C/T]CTTGTGATGGTACAA	146691
rs186344316	snp	G/T	0.00199481	0.0315187	upstream-variant-2KB, intron-variant	TOM1L2, DRC3	GRCh38.p7	17:17974022	CCATAGAAGAGGACT[G/T]TTTGGGCCTTGGCCC	146691
rs186369255	snp	C/G	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17904157	TTTTGAGACACCTCA[C/G]AGCAGAGGCAACAAG	146691
rs186380940	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17925663	CCTGGCCAACATAGC[A/G]ACCTCACCTCGTGTC	146691
rs186397022	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17855789	GAGAAGCTGTGAATC[C/T]CTTCCTATGTCACTT	146691
rs186417228	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17944982	ACATTGCAGCAGATG[C/T]TGCCCGCACTGCCGC	146691
rs186433475	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17911506	ATTTTAGGTTTTGAC[A/G]ATTTAGGTGACAAAA	146691
rs186476744	snp	A/G	0.0023933	0.0345097	intron-variant	TOM1L2	GRCh38.p7	17:17877485	TAAGCAGACAGTGGT[A/G]TTTCTCCACATGGAA	146691
rs186478616	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17946664	AGGCTCATGGGTGCA[C/G]AGGCTGCAGGAGGCC	146691
rs186484570	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17900778	TGATTTCTGCAAATA[C/T]GGGACTTAACCGGCT	146691
rs186486908	snp	C/G	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17951266	CTCTGGCAGGGACCA[C/G]ATCTGAGATCCAGTC	146691
rs186496987	snp	A/G	0.00199481	0.0315187	upstream-variant-2KB, intron-variant	TOM1L2, DRC3	GRCh38.p7	17:17973250	TTTTTAAGGGGTTCC[A/G]TCTTCCAGCCTCCTT	146691
rs186501519	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17921413	GGGTGTGCTCTCTAG[A/T]AGCAGAGCCACTGGT	146691
rs186507727	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17950288	CAGTCTTCCGAGTAG[C/T]TGGGATTACTGGAAT	146691
rs186508426	snp	A/G	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17852074	GGGAGGTACCCTTCC[A/G]GGGCTCACTTGCAAG	146691
rs186511177	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17930367	AAGTGGTTAAAAAAA[A/G]GGGGGGTCTGGGAAT	146691
rs186562872	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17915944	ACTCTCTTGATTGTA[C/T]CTTTTAATGCACAAA	146691
rs186574515	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17883442	CAGCCTCCAGAAAGG[A/G]CAATCCCCTGGGCCA	146691
rs186664904	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17966835	ACTTAATAATTATAA[A/G]TTCCTTCCAGTTATC	146691
rs186678628	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17967871	CCACGGCCTCCCAAA[A/G]TGCTGGATTACAGGT	146691
rs186693139	snp	A/C	0.00478085	0.0486577	intron-variant	TOM1L2	GRCh38.p7	17:17927378	GGCCAGCTGCAGAGG[A/C]TGTGGAGAGAGGCCT	146691
rs186782235	snp	G/T	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17936465	ACAAGCATACCCTTT[G/T]ACATGGTAATTCTAT	146691
rs186795198	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17856863	CCTTGCAGGTCTGTG[G/T]GCCAGGAAAGCTCTG	146691
rs186818700	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17905571	AGAGACAGGGTCTTA[C/G]TCTGTCGCCCAGGCT	146691
rs187065346	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17857613	GATTATGCAAAAATA[C/G]GAGGGGAAATTTGGC	146691
rs187102203	snp	A/G	0.00557542	0.0525036	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17845690	GGCTGGGGCCTCTGG[A/G]TGCACCTGGGCCATC	146691
rs187117142	snp	C/T	0.0023933	0.0345097	intron-variant	TOM1L2	GRCh38.p7	17:17921874	CCCTCGCCCTCGTGC[C/T]CACCATTCACCACCA	146691
rs187119469	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17891875	GAACAGGGACGAGGG[A/G]CAACCCTAGGGTAAA	146691
rs187138590	snp	C/T	0.00279162	0.0372561	intron-variant	TOM1L2	GRCh38.p7	17:17960565	CTGGTCTCGAACTCC[C/T]GAGCTCAAGTGATCC	146691
rs187143908	snp	C/G	0.0023933	0.0345097	intron-variant	TOM1L2	GRCh38.p7	17:17901665	CCCCATTATTATCTT[C/G]CTCTATTGCATGTCT	146691
rs187145330	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17941995	CTTTCCCACAAAAAC[A/G]TAGCACAAAAGAGCT	146691
rs187145970	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17938163	AGAAATGAGAGGGAG[A/G]CAGTTAGATCCAATT	146691
rs187150286	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17964355	TTTACACCGTTTTCC[C/T]TTCCTAATATCCCAA	146691
rs187163545	snp	A/G	0.0023933	0.0345097	intron-variant	TOM1L2	GRCh38.p7	17:17895423	GGACAAAACATAGCC[A/G]TAAAGAAAGGTCCAT	146691
rs187176752	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17867241	GGGTGGCTTAACCAC[C/T]TTACCTTGGAGCTGC	146691
rs187247880	snp	C/G	0.0023933	0.0345097	intron-variant	TOM1L2	GRCh38.p7	17:17947634	TAAGTTCGGTTAAGC[C/G]TTCCAGTCTGTGGTA	146691
rs187277095	snp	C/T	0.0023933	0.0345097	intron-variant	TOM1L2	GRCh38.p7	17:17969614	AGCCATCATCATCTT[C/T]AGTCAAGCATCTTAT	146691
rs187287829	snp	C/T	0.00557542	0.0525036	intron-variant	TOM1L2	GRCh38.p7	17:17872014	CAGGCAGGAGAGGGG[C/T]TCTCAAAAAGCTGCC	146691
rs187298113	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17863963	CCTCAACCTCCTGGG[C/T]TCAGGAGATTCTCCT	146691
rs187301683	snp	A/G	0.00636936	0.0560724	intron-variant	TOM1L2	GRCh38.p7	17:17957888	GAGGTCCGGAGATCA[A/G]GACCATCCTGGCTAA	146691
rs187304003	snp	C/T	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17897805	CTCAGTTTCATCATC[C/T]GTACGGGGGAGGATA	146691
rs187307377	snp	C/T	0.0023933	0.0345097	intron-variant	TOM1L2	GRCh38.p7	17:17939458	TACATTTTAAAAGTA[C/T]AATCACAGTATTGTG	146691
rs187308465	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17917563	CTTAGCCTTCCAAGT[A/G]GCTGGGAATACATGT	146691
rs187309196	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17911005	TGCTTCTGAAGTCAC[C/T]ATATTTAACATCAAA	146691
rs187331191	snp	C/T	0.00358779	0.0422022	intron-variant	TOM1L2	GRCh38.p7	17:17941569	ACGAGGAGATATCCA[C/T]GGGCAGTCTAAGTCT	146691
rs187355154	snp	C/G	0.00636936	0.0560724	intron-variant	TOM1L2	GRCh38.p7	17:17896587	AGGAGGTCCTCCCTG[C/G]GCTGGCAAGAGCCGC	146691
rs187369801	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17917401	TCCCTTGAGATTTCA[C/T]GTGAATTTTAGGATG	146691
rs187375080	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17917116	AATGAGCCGAGATCA[C/T]GCCACTGCACTCCAG	146691
rs187381567	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17956863	TCTCCCTCCACATCT[C/T]CCTGCAAGCTGAGGG	146691
rs187387829	snp	C/T			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847368	CTGGGCCACTCTGCC[C/T]GCTCTTCCTGGGAGG	146691
rs187390700	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17873309	TGACAGCTTTAACAC[A/G]TACTTCCCATTTATT	146691
rs187440414	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17878644	AGACTGACAACGGAG[A/G]GCCAGACACAAATGG	146691
rs187473884	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17961645	TTGGGAGGCCGAGGC[A/G]GGCGCATCATGAGGT	146691
rs187494347	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17922407	GGGGCTTTTCAACAG[A/G]AGTGACAAGAATATT	146691
rs187562380	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17888810	AGGGAAAGGCTCAGG[A/G]ATGGCATAGAGTGGG	146691
rs187590165	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17959837	TCCCAGACTACAAGG[C/T]TTATGCTTCATTAAT	146691
rs187605819	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17939669	ACTATTCTACTTTTG[C/T]ATGTTTAAAATTTTC	146691
rs187686024	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17853906	TGCTAGATTGTATTT[A/G]GCTTTCAATTCTTAT	146691
rs187694602	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17902059	TACACACCTATAATC[C/T]CAGCTACTCAGGAGG	146691
rs187717027	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17908138	CACTGTAGGTGTGGT[A/G]TTGGGTGTTTCACGT	146691
rs187740531	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17946973	CAAGTGATCAGCCCT[C/T]CTCAGCCTCCCAAAG	146691
rs187740982	snp	C/G	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17942787	AGTTAGTATAGAAAA[C/G]GAAGCAGTCAGAATT	146691
rs187744470	snp	A/C	0.00398564	0.0444627	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17859881	GCGAGACTCCATCTC[A/C]AAAAAAGCAATCTGC	146691
rs187749093	snp	A/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17928088	AATTGTAGAAGCTCA[A/T]TGATGAGTATGTGGG	146691
rs187750425	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17886206	GACCCATTTGAAGTT[A/C]AAAGGTCAGTTTCCA	146691
rs187869429	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17958594	CTAAATGACTGGCAA[C/G]AGGCTGTGAGCTAAA	146691
rs187888734	snp	A/C	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17943265	TCTCCAATCCACTGT[A/C]ACAGTCACTTTAAAA	146691
rs187889153	snp	C/T	0.00874735	0.0655527	intron-variant	TOM1L2	GRCh38.p7	17:17918256	GCAGTTTTTCTTTTT[C/T]TTTTTGTTTTGTGGT	146691
rs187890657	snp	C/G	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17854441	CAGACTAGGGGCTGG[C/G]CCAGCAGATTCCTAA	146691
rs187896804	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17922962	TTGGCCAGGCACCAA[C/G]TAGCCTGTGAGGCCA	146691
rs187898776	snp	C/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17879139	TCTCAGGACACCTTG[C/G]GGGTGAGGTGCCACT	146691
rs187899529	snp	A/G	0.0023933	0.0345097	intron-variant	TOM1L2	GRCh38.p7	17:17853025	CAATGCCTAAGGCTG[A/G]CACTTCCTTGCCCTT	146691
rs187903136	snp	A/C/G	0.0023933	0.0345097	intron-variant	TOM1L2	GRCh38.p7	17:17903182	TCTCTCCCTGCCCCC[A/C/G]ACCCAGCACTCGTTA	146691
rs187903137	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17954189	CAGGGCCAAAGGCCA[C/T]GCTGAGCACAGAAAA	146691
rs187958674	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17933150	ACCCAGGAACTTTTT[G/T]TCTTCTTCCTCTGCC	146691
rs188053682	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17905976	CTCAAACACATCAGA[C/T]ACCCTCTGTCCCAGG	146691
rs188108612	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17873828	CTGTCATGCTGCAGC[A/G]GCCTCCATGGCACGG	146691
rs188167986	snp	A/T	0.00279162	0.0372561	intron-variant	TOM1L2	GRCh38.p7	17:17868053	TGGGTGAAAATACTC[A/T]TATTAGTTAGCTCCT	146691
rs188174407	snp	C/T	0.00636936	0.0560724	intron-variant	TOM1L2	GRCh38.p7	17:17892413	GCCTCTGCCACAGCA[C/T]TAATCACCCAGGCTG	146691
rs188176264	snp	C/G	0.00398564	0.0444627	intron-variant	TOM1L2	GRCh38.p7	17:17855170	GTCAGCTGATTCTCA[C/G]TTGGAACTGCAGGCA	146691
rs188176454	snp	C/T	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17954884	CTCACACAGATACTA[C/T]GCTCTAAGGCCAAGA	146691
rs188180683	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17915269	GATCCAAACTCAGGC[C/T]TTGCTAGCAGGTGAG	146691
rs188184739	snp	A/C	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17934864	TTAACAGGGGAAAAC[A/C]TTCAGAATGAAACAC	146691
rs188199834	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17886493	CGCTGGCTGCCTCCA[C/T]CTGGTTCAAAATCCA	146691
rs188227236	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17914500	CCACATGCATGAAAA[A/G]GGCAGAGAGGGGGTA	146691
rs188233856	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17928518	AGAGAACACAGAAGG[C/T]GACACCCTCCCTTTA	146691
rs188244445	snp	C/T	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17957663	TATATAAAATATATA[C/T]AAAATATGTATATGT	146691
rs188247405	snp	C/T	0.00398564	0.0444627	intron-variant	TOM1L2	GRCh38.p7	17:17877658	TGTCCACAGTGCTGC[C/T]CAGCTCCTGAATCTG	146691
rs188316864	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17888325	TTCCTTTGGACCGTA[C/T]ACAAAACCCCAGAAT	146691
rs188326801	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17883902	TACTGGGATGAGGTG[C/T]CTCTCCCAGACCCTG	146691
rs188327042	snp	A/G/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17910333	TGAGGGCAGGGACTA[A/G/T]GTCTGTCTTGCCTTC	146691
rs188327273	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17948903	CTGACCCTGTGAGGG[A/G]TGGGGGGAAAGAGTT	146691
rs188333342	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17929580	AGGTTGTGGTGAGCC[A/G]AGATCGCACCATTGT	146691
rs188334639	snp	A/G	0.00478085	0.0486577	intron-variant	TOM1L2	GRCh38.p7	17:17848735	AGGTGCTCTGGCAGC[A/G]GGGGCTCCAAGATGA	146691
rs188480751	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17861798	CGATCTCAGATTTTG[C/T]GCACCTCAACATCCC	146691
rs188536712	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17938461	CCGCTCTGACTAGGA[C/T]GTTCTATATAATAAA	146691
rs188545013	snp	C/G	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17908560	GGGTTAATATCCAGA[C/G]TACGTAAAGAACTCC	146691
rs188676020	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17954375	TAGAGTGCAATGGTG[C/T]AATCTTGGCTCACTG	146691
rs188698341	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17940268	AGATGAGATGAGCTT[A/T]TACGGGTCAAGCACT	146691
rs188707542	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17919615	GATTCCCCATAAGTC[C/T]ACATTTCCTGGACCC	146691
rs188736861	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17959438	CCTTGTTTCCACAAC[C/T]TGCAAAAATTAGAGG	146691
rs188742768	snp	A/G	0.00318978	0.0398085	intron-variant	TOM1L2	GRCh38.p7	17:17898248	ACAAAGAGGAAACTG[A/G]TATCTAGAGAAGGAG	146691
rs188779427	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17887505	ATTGGGCATGGGTCA[C/G]AGCTGTCCCCCAGGC	146691
rs188818770	snp	C/T	0.000627487	0.0177017	intron-variant	TOM1L2	GRCh38.p7	17:17850999	CCCCCACACAGCCAG[C/T]GAGGGGAGACAGAAC	146691
rs188820433	snp	A/C	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17862998	TACTCCCAGTGCACC[A/C]CATGCCGGAGGAGCC	146691
rs188826834	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17939856	ATGTAGGAGGCTCTG[C/T]AGTAGCCTCTACTTC	146691
rs188830898	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17875350	TACCACAGTGCCAGC[C/T]GGCCACCTGCATGTC	146691
rs188835145	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17918995	GTGAGATGAGAGCTC[A/G]GTTCCCAGCTGTCCC	146691
rs188839204	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17899409	AGATAAAATCTTGCA[C/G]AATTATAGACAGTAC	146691
rs188839975	snp	G/T	0.000205884	0.0101439	intron-variant	TOM1L2	GRCh38.p7	17:17866275	AGTAGGTAGGCCCTT[G/T]TGTCCCTGTGAGACA	146691
rs188910664	snp	A/G	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17913728	GAATGCACTGACCCT[A/G]AGGATAAGTTATCAT	146691
rs188938931	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17944297	ATGCTGAGCAGAGGG[C/T]TCCTTCCTGACCTTG	146691
rs188940960	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17915988	GATTGTCCCATTTAT[C/T]TATTTTTTCTTTTGT	146691
rs188949486	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17923521	AGACCCTGTCTCTAC[A/C]AAAAAAAATTTTTTT	146691
rs188968852	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17844537	CTTTCCCTCTAGCCC[A/C]GGCCAGCAACAACCC	146691
rs188973187	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17870344	AGACTTACTGATGCC[C/T]TTGTTCAAACTTGCT	146691
rs188978382	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	TOM1L2, DRC3	GRCh38.p7	17:17973313	ACTTTTCCCAGAATT[C/T]AGCCATCATAACTGA	146691
rs188984654	snp	C/T	0.000696009	0.0186419	intron-variant, synonymous-codon, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17893760	GAAATCTCGGTTGGC[C/T]ACAAGGATGTGGAAG	146691
rs188984784	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17962609	ATGAGCCACCGCGAC[C/T]GGCCCAATGTGAATA	146691
rs189027382	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17881918	CAGTCATGACATTGT[C/T]GCAAATAGTAAATAA	146691
rs189054676	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17925094	CTTCCCCTTCTGCCA[C/T]GAGTAAAAGCTTCCT	146691
rs189090653	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17964065	CTGCCTGTAGGAAGA[A/G]GTGAGGGCTGATGGG	146691
rs189163747	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17932523	TGGGCAGCAGTGTAA[A/C]ACTGTTTTACAAACA	146691
rs189184401	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17891380	GGTAAAAGCTAGGAG[A/G]AGCTGGAAAGTGTGG	146691
rs189228933	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17962118	AGTCAGTCATGAAAG[A/G]ATAAATACTATATGA	146691
rs189317890	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17903580	ATCGCGCCACTGCAC[C/T]CCAGCCTGGGCGACA	146691
rs189381137	snp	C/T	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17944648	TCTTGTGAAAATCTA[C/T]GAGCTAACACAATGA	146691
rs189437233	snp	C/G	0.00438332	0.0466095	intron-variant	TOM1L2	GRCh38.p7	17:17863358	GGCTTGAGACATCAG[C/G]AAAGACTCAAAACCA	146691
rs189529619	snp	C/T	0.00438332	0.0466095	intron-variant	TOM1L2	GRCh38.p7	17:17854669	AGCTGGGATTACAGG[C/T]GTGAGCCACCACACC	146691
rs189591390	snp	A/G	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17895003	CATGCATAAAATAAT[A/G]CACATAGCAAAGTAT	146691
rs189623076	snp	A/G	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17938108	TCCCTCTCACCCAGC[A/G]TGGTGCAATGGGAAG	146691
rs189642815	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17945637	ACATCTTAGTTAATC[A/T]TTGATATTTTGTGAG	146691
rs189649689	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17916516	TCCCAGCACCATTTG[C/T]TGAAAAGACTGTCCT	146691
rs189651562	snp	C/T			intron-variant, downstream-variant-500B	TOM1L2, LOC100507131	GRCh38.p7	17:17857766	CGGCTGGTGACTCCT[C/T]ACCATTCCTTGGGTT	146691
rs189653968	snp	A/G	0.00438332	0.0466095	intron-variant	TOM1L2	GRCh38.p7	17:17884103	GGGATGCCCCTAAAG[A/G]GACCTTCCCAGGGCT	146691
rs189664582	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17956570	TCCTTGGGGAGGTTC[G/T]GGCCGCATAGGAGCC	146691
rs189703979	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17909355	TAAACAGCCTGTGTC[C/T]ATCAATTAAAGAATG	146691
rs189708003	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17876507	AATTAGTCTTGTTCT[A/G]GTGTCTAAGAAGACA	146691
rs189762501	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17948262	AAATACGCCCTAGTC[A/C]CTACCTTGGAGAGAG	146691
rs189763684	snp	A/C	0.00517822	0.0506191	intron-variant	TOM1L2	GRCh38.p7	17:17952545	CACAGGTGCGTGCTG[A/C]CACCCCTGGCTAAGT	146691
rs189773544	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17931874	AAATAATTCTTATCA[C/T]ACAGGTCTCCAAATA	146691
rs189792214	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17912805	CGGGCAGAGGCTGCA[A/C]TCTCGGCACTTTGGG	146691
rs189815724	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17880177	ATCCTATTCTACAAA[C/G]CTCTGAGTTATAGAC	146691
rs189856202	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17888952	AGCTGCCGGAAGGGA[A/C]GTCTTTGGTGCCCCT	146691
rs189867274	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17959399	GCTGTCAGAAATGTC[A/T]TACATCACAGACACC	146691
rs189889450	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17851785	AAGTTCAGCTGAGCA[C/T]TGGGGCGCAGCAGCC	146691
rs189907731	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17930472	AGGCCCCTCCTGACA[C/T]TTGGGGCTCCTAAGT	146691
rs189953454	snp	C/T	0.00953873	0.0683987	intron-variant	TOM1L2	GRCh38.p7	17:17851403	ACAGCCTGCCCAGAG[C/T]GGGGTACAGGTGCTC	146691
rs189973574	snp	C/G	0.00279162	0.0372561	intron-variant	TOM1L2	GRCh38.p7	17:17929186	GCTGCTCAGCAGCGT[C/G]AGGCGGGGAAGTCAA	146691
rs190002405	snp	A/C	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17971213	ACAGTCAATGTGCAG[A/C]GTACTACAAAGAATA	146691
rs190015609	snp	C/G	0.0232847	0.105357	intron-variant	TOM1L2	GRCh38.p7	17:17903405	GAGGCGGGCGGATCA[C/G]GAGGTAAGGGGATCG	146691
rs190020732	snp	A/C	0.00517822	0.0506191	intron-variant	TOM1L2	GRCh38.p7	17:17899983	TTGGGAGACCAAGGC[A/C]GGTGGATAACCTGAG	146691
rs190023641	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17936580	AAGGAAAAAAAGAAA[A/C]GAAATAATCTAAATG	146691
rs190055023	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17961288	TGAACCAAGTGCAGG[C/G]GTTCACGTCCTATAA	146691
rs190062714	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17942554	GCCGATATGTATGGG[C/T]CGATATGTACACCTT	146691
rs190095140	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17864047	AATTTTTTTGTATTT[C/T]TAGTAGAGATGAGGT	146691
rs190114974	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17911062	AAGCCGCTGGATTGC[A/G]AGGCTCCTCCAAACA	146691
rs190152096	snp	C/T	0.00279162	0.0372561	intron-variant	TOM1L2	GRCh38.p7	17:17950369	TTACCAAGTTGGCCG[C/T]GCTTGTCTCGAACTC	146691
rs190254223	snp	A/C	0.0209421	0.100162	intron-variant	TOM1L2	GRCh38.p7	17:17911680	TTATTTTTTATTGAT[A/C]ATTCTTGGGTGTTTC	146691
rs190270353	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17956256	TGCGTTTACAATCCC[G/T]GAGCTAGACACAAAG	146691
rs190290115	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17864462	TGATCCACCCGCCTC[A/G]GCCTCCCAAAGTGCT	146691
rs190295829	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17889736	CCCCCAAGCCACAAA[C/T]AGTCAAAAGCCAGTT	146691
rs190326813	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17970083	TTTTTGAGACAGAGT[C/T]TCACTCTGTCGCCCA	146691
rs190341312	snp	A/T	0.0023933	0.0345097	intron-variant	TOM1L2	GRCh38.p7	17:17850467	AAAGCACTGTGTGTA[A/T]ACTTCACAATTAAAA	146691
rs190494455	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17868953	TTTTTCTTACTAGAG[A/T]TTTTTTTTCCCTTTA	146691
rs190510444	snp	A/G	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17915481	TATATCTTCTTTGGA[A/G]ACATATCTATTCAAT	146691
rs190513487	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17852134	TCTGTCTATAGCTGG[C/T]TTCACCCAATGCCAT	146691
rs190543165	snp	C/T	0.00279162	0.0372561	intron-variant	TOM1L2	GRCh38.p7	17:17921447	TGATGTATGCCGTTC[C/T]TTGTACTTAATGGAA	146691
rs190544229	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17955840	AGTTTCTTCCTCCTG[C/G]TGGGTTCGTAGTCTC	146691
rs190567944	snp	C/T	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17877560	GCTGGCTTTTGACTG[C/T]CAGGGGAAGAAGGGG	146691
rs190572108	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17960295	GGGTTCAAATCCCTG[C/T]TCTGCCACTGATAAT	146691
rs190573009	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17901186	ATCTCTCTCCCCGGG[A/G]GAAAAGCTTCAGAGA	146691
rs190580978	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17941613	CTCACCTGCCCGTCC[A/C]TAAAGGCAGAGTGGA	146691
rs190592513	snp	A/G	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17874357	CTCACTGCAACCTCC[A/G]CCTCCCAGGTTCAAG	146691
rs190643600	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17845199	GGATAGGAGGTGCAA[C/G]CAGGCCACCTGAGGG	146691
rs190687645	snp	A/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17966244	ATCCAATCTTGCAAC[A/T]ACTTTCTATCTGATC	146691
rs190700789	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17946290	ATTCACAGAGTTGTG[C/T]AACCATCACCACTAT	146691
rs190725344	snp	C/T	0.0111196	0.0737302	intron-variant	TOM1L2	GRCh38.p7	17:17927381	CAGCTGCAGAGGCTG[C/T]GGAGAGAGGCCTCTC	146691
rs190728659	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17917417	GTGAATTTTAGGATG[C/G]ATTTTTCTATTTCTG	146691
rs190732791	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17938645	ATAAATGCACAGGGA[C/T]GCAACCCAGCAGGCA	146691
rs190749303	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17892810	GGTATGTGACTTCCA[A/G]GGCTAGGTCATCAAG	146691
rs190753984	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17967639	GGAGATGCAGTCTCG[C/T]TCTGTCATTCAGGCT	146691
rs190779850	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17844050	TGGGTGAGACGTCCC[C/T]AAAGCCGACAGTGCA	146691
rs190788582	snp	C/T	0.00597247	0.0543191	intron-variant	TOM1L2	GRCh38.p7	17:17900127	CTGAGGCAGGAGAAT[C/T]GCTTGAACCTGGGAG	146691
rs190798808	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17865351	CCAAGAAGCCAAAGA[A/G]CTGAAACCTATCTGC	146691
rs190803135	snp	A/C	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17935922	GTGCAACAGTCTGAA[A/C]TGGTCTCCCAGAAGG	146691
rs190807882	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17941190	GGAGGGGCTACTGGC[A/C]CCCTGAAGTTCCTGT	146691
rs190904963	snp	C/T	0.0023933	0.0345097	intron-variant	TOM1L2	GRCh38.p7	17:17871397	TTCAGAGGCCAAGTG[C/T]GGTGCCTCATGCCTG	146691
rs190982757	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17907007	CCGCTTTCCCACTCC[C/T]GGCCGTGTCTGCCCC	146691
rs191005293	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17921997	GACACATCCCAGAGA[C/T]GTGAATGCCACTCCT	146691
rs191061716	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17920851	ATGTTGGCCAGGCTG[A/G]TCTCAAACTCCTGAC	146691
rs191078231	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17877202	CCAAAAGTGCTTTGC[A/G]ATGTGCAGGAGGCAA	146691
rs191097137	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17959630	TTTCCTATTTCGACT[A/G]ATGACGTGCCAGAAA	146691
rs191159445	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17856100	GTGTGGGCAGAGACA[A/G]GCACCACCACCAGCT	146691
rs191186748	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17925856	TGAGACCCTGTCTCA[A/C]AAAAAAAAAAAAAAA	146691
rs191218095	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17904403	GAGTTGCCAACATAT[A/T]TGTATATTGCTCAAA	146691
rs191245951	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	TOM1L2, DRC3	GRCh38.p7	17:17974139	AAATGAACTCTGCCA[C/T]GTGCTAAGTGTATGA	146691
rs191340185	snp	A/C/T	0.00438769	0.0466326	intron-variant	TOM1L2	GRCh38.p7	17:17878028	CCAGAGCAAATCCCC[A/C/T]CTGTCAGCAGGAATT	146691
rs191351526	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17918007	TTTCCATATATTTAT[A/G]TCTTCTTTCTTCTTT	146691
rs191355285	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17854281	GTGGGAGGCCGAGGA[C/T]GCGCTCCTTGTCAGG	146691
rs191361483	snp	A/G	0.00279162	0.0372561	intron-variant	TOM1L2	GRCh38.p7	17:17951600	GAAGAATGGTGACCA[A/G]AGGGTTTTTAGCAAA	146691
rs191370195	snp	A/G/T	0.00398564	0.0444627	intron-variant	TOM1L2	GRCh38.p7	17:17878979	GGTAGACTGCAGGCC[A/G/T]CCCACTCCTGGACCC	146691
rs191390196	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17958152	CCTTAAGCTTTAGGT[A/C]TGAAATGAACTTGGA	146691
rs191396229	snp	C/T	0.00517822	0.0506191	intron-variant	TOM1L2	GRCh38.p7	17:17939469	AGTACAATCACAGTA[C/T]TGTGATTGTTTCTAA	146691
rs191405567	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17887681	GGGTTTCATCATGTG[G/T]CCTAGGCTGGTCTTG	146691
rs191415718	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17909799	CTTTGGGAGGCTGAG[C/G]CAGGAGGGTTACTTG	146691
rs191497312	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17915382	CTTACCAGGTGTGAA[A/G]TGGTATCCCAGTGTG	146691
rs191535481	snp	C/T	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17955001	CCCTAGAGCAATGTC[C/T]TTATGTTCAAAAAGC	146691
rs191541081	snp	A/G	0.00636936	0.0560724	intron-variant	TOM1L2	GRCh38.p7	17:17962956	ACAGAGTGAGACTCC[A/G]TCTCAAAAAAAAAAA	146691
rs191546086	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17935215	TCTACAAGTTGGATG[C/T]TGTTAACTTTGGGGA	146691
rs191584319	snp	A/G	0.00398564	0.0444627	intron-variant	TOM1L2	GRCh38.p7	17:17856867	GCAGGTCTGTGGGCC[A/G]GGAAAGCTCTGCTAC	146691
rs191587909	snp	A/G	0	0	intron-variant	TOM1L2	GRCh38.p7	17:17901712	GCCCTCTCCAGCTTA[A/G]AAGATAGAACACAAA	146691
rs191598663	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17905623	GGTTCATCACAGCCT[C/T]GAACTCCTAGGCGTA	146691
rs191614210	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17931517	CTCAGGAGAACTGGG[A/G]GAGCAATAGCTGGCA	146691
rs191616358	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17933395	GTAAGAGAATATAGC[C/T]GGGCACATAGGCAAT	146691
rs191622862	snp	A/C	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17853388	TTAAGGGGTCAGGGG[A/C]CTTAAACCTTCAGAT	146691
rs191641335	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17892231	GGAATGGACAGAGGC[C/T]CCTCTCCAGCTGCAC	146691
rs191646031	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17914590	CTCTCCTCCTCCACT[C/T]TCCCCATCTTGTAGA	146691
rs191806812	snp	C/T	0.00279162	0.0372561	intron-variant	TOM1L2	GRCh38.p7	17:17956927	GTTCTCACAGTGCAG[C/T]GGCGGGCTGAAGGGC	146691
rs191884913	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17883472	AGGTGCGGTGGCTTA[A/C]GCCTGTAATCTCAGC	146691
rs191923008	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17867536	CTTTGAGCAACTGTC[A/G]AAGGCCAGGTCATCC	146691
rs191950905	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17927195	AAAAACCAACAGCAT[A/G]AAACTGCATTCTTCA	146691
rs191968214	snp	C/T	0.0023933	0.0345097	intron-variant	TOM1L2	GRCh38.p7	17:17957682	ATATGTATATGTATA[C/T]ATTTACCTGTGTGCA	146691
rs191998900	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17854522	TTATTTAGTTATTTA[A/T]TTAATTAATTAATTT	146691
rs192046587	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17943849	TTGCCAGGGCCCCAC[A/G]TGAACATCCAGAGCC	146691
rs192060418	snp	C/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17923093	GGGCTCATACCTGCT[C/G]TGCTCATTAAAGCCA	146691
rs192069818	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17903194	CCCCACCCAGCACTC[A/G]TTATGCATATGTTTA	146691
rs192088174	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17962190	TTATATGAGGTTCCT[A/G]GAGTAGTCAAATTCA	146691
rs192099711	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17917174	AAAAAAATTAAAAAA[A/T]TTAAAAAATTAGCTG	146691
rs192130442	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17872414	TTAGGTTAACTTTGA[C/T]AGACCATCCTCCCCT	146691
rs192167760	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17848089	CTGGGGGTGGGGCAG[A/G]GTAAGCTGGAGGGGC	146691
rs192236847	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17897809	GTTTCATCATCTGTA[C/T]GGGGGAGGATAGTAA	146691
rs192237814	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17873540	GGATTTAGAGGAGAA[C/T]CAAACCAGATTCCTC	146691
rs192246588	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17897484	AGAAGTTGACCTGGT[A/G]ACCTGTTACAGTTTC	146691
rs192262088	snp	A/C	0.00051191	0.0159904	intron-variant	TOM1L2	GRCh38.p7	17:17848797	GGCAACAAAAGGGGG[A/C]TGTAAGGCCACTGGC	146691
rs192270195	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17929284	TTCTCCATCTCTTCT[A/G]CTTAGAGCTGCTTTG	146691
rs192299536	snp	C/G	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17971318	CAGAAAGGGCACAAG[C/G]TCATATGGAGTCACT	146691
rs192302744	snp	G/T	0.00398564	0.0444627	intron-variant	TOM1L2	GRCh38.p7	17:17947210	TCAGTTTTATACGGT[G/T]GGGGGGTCTCACTAT	146691
rs192310201	snp	C/G	0.00279162	0.0372561	intron-variant	TOM1L2	GRCh38.p7	17:17928171	CAACAAAAAAAATCA[C/G]TAGGAGACAGCATAA	146691
rs192325904	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17908489	AGGCATCAAAGGACA[C/T]AACACAGTGAACCTG	146691
rs192330704	snp	G/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17850592	AATGGAAAAGATACT[G/T]GGGGGAAGGCAAGTG	146691
rs192346676	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17968223	CAGAGCCTGGCACAG[A/G]CCTGGCCCCCCACAG	146691
rs192372400	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17868909	TTTTTTCTTTTTTCT[C/T]TTTTTTTAAGATGGG	146691
rs192405035	snp	C/T	0.00279162	0.0372561	intron-variant	TOM1L2	GRCh38.p7	17:17942999	ATATGATGCCTGGAA[C/T]CTGCTTCAAAATAAT	146691
rs192415363	snp	C/T	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17902464	TGTGCTTGCATCCTG[C/T]ATGTGCCCTTCCAAG	146691
rs192462222	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17895444	AAAGGTCCATAACTG[A/G]AACACTGACTGAATG	146691
rs192487679	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17938298	GCCACCTGGCAGGAC[A/G]TTCTAGAAGGGGTGC	146691
rs192494886	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17846033	CAGGGTCCTGGGTCG[A/G]GCAGCACTTGCTCTT	146691
rs192564870	snp	C/G	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17954532	TGGCCAGGCTAGTCT[C/G]GAACTACTGACCTCA	146691
rs192634024	snp	A/C	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17874027	GTGGCACAATCTCGG[A/C]TCACTGCAAGCTCCG	146691
rs192658231	snp	G/T	0.000798403	0.0199641	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17860439	CTCAGATCCACCAGG[G/T]GAAGACCAGCATGGA	146691
rs192672275	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17886227	TCAGTTTCCAAAAAG[C/T]CTCCTTAATTATGAC	146691
rs192712592	snp	A/C	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17948524	AGGTATGGTGGTGCA[A/C]GTCTGTAATCCCAGC	146691
rs192755902	snp	A/G	0.00478085	0.0486577	intron-variant	TOM1L2	GRCh38.p7	17:17961729	ATACAAAAATTAGCC[A/G]GGCGTGGTGGCAGGC	146691
rs192763013	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17922441	GTCTGAGACAGATCG[C/T]TCTGGTAACAGCATG	146691
rs192764265	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17843954	GGCACTGGGGGAGGC[A/G]AGCACTTCAGGGGCT	146691
rs192854205	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17891495	CCAGTGAAGAAGGCT[A/G]TGTCTGCCCTCAGCC	146691
rs192869423	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17932623	TCTCTGGAGCAGGCA[C/T]GGGATGTGGTGGGGA	146691
rs192932736	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17908877	TATGGAAAACAGGAC[A/G]GTAGTTAAAACACAG	146691
rs192946362	snp	A/C	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17861896	GGAAGACTAGATAAA[A/C]ACAAAGTAACATTAA	146691
rs192963602	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17948149	TTTCATTAAGTTCCT[A/T]AGTCAAATAGTTTCA	146691
rs193016756	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17958856	CTCATCCCACCTTAC[C/T]TCCGGAAAGGGGAGA	146691
rs193019962	snp	C/T	0.0023933	0.0345097	intron-variant	TOM1L2	GRCh38.p7	17:17874572	CACTATGCCTGGCCT[C/T]CATTACTTTAAAAAA	146691
rs193025080	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17918437	AAGGCAGCATCGTTG[C/T]GCCTATATATATTTT	146691
rs193065265	snp	C/G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17913979	GAGAGACTACTACCC[C/G/T]CTAGCCAGCTGGCCT	146691
rs193079680	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17866712	ACCTTCCCATCAGGG[A/G]TGCCTGCTAGCTCTG	146691
rs193104589	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17954256	GGTAAGAGAAAAGAC[A/G]GGAAGAAGCCCAGTC	146691
rs193175129	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17928789	TAGCTGCTGTCTGTG[C/T]CTCAGGATTTTTTTT	146691
rs193178991	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17886623	CTGGGGAAAAAACAC[A/G]TGGCAGTTCTTCCTG	146691
rs193184127	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17969685	TCACAGGTCACAGAC[A/G]GGCCAGTTGTTTCAC	146691
rs193213610	snp	C/T	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17939731	GATAAAATTGACACA[C/T]TCAATATTCTTAGAG	146691
rs193215242	snp	C/T	0.00279162	0.0372561	intron-variant	TOM1L2	GRCh38.p7	17:17898268	TAGAGAAGGAGTTGG[C/T]CTCAGTCTCAGAGCA	146691
rs199505893	in-del	-/C/CTTTTTTTTT			intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17858232	TTTCCTACATTTTTT[-/C/CTTTTTTTTT]TTTTCTCTTTTCTAG	146691
rs199528113	in-del	-/C			intron-variant	TOM1L2	GRCh38.p7	17:17928159	AATTTTCTGTAACAA[-/C]AAAAAAAATCAGTAG	146691
rs199553714	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17950509	ATCTTACCAAGGCCG[A/G]CCTCAAGCTCCTGGG	146691
rs199563013	snp	A/G	3.29587e-05	0.00405934	missense, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17882784	GGAGCAGGAGGCGGC[A/G]AGGAATAGGAACCAG	146691
rs199586093	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17956703	CGGCACTGCTGGGGG[A/G]ATGGCACACCCTCCG	146691
rs199625924	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17912870	AGCGAGCCGAGATCA[C/T]GCCACTGCACTCCAG	146691
rs199631147	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17946960	GAGCTCCTGACCTCA[A/G]GTGATCAGCCCTCCT	146691
rs199699086	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17894932	CAAAACTCTGTCTCA[A/C]AAACATACATACATA	146691
rs199730242	snp	A/G	0.280226	0.248166	intron-variant	TOM1L2	GRCh38.p7	17:17869324	AAAAAAAAAAAAAAA[A/G]AAATCCGGCTCCCAC	146691
rs199774885	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17884596	GGCTCACCCGTTCTG[C/T]AGTAGGTCTTTCTAG	146691
rs199826035	in-del	-/CAA	0.0178098	0.0926698	intron-variant	TOM1L2	GRCh38.p7	17:17956062	TCATGGAGTAAGCAG[-/CAA]CATTTGTTTCAAAGA	146691
rs199832973	snp	C/T	1.65184e-05	0.00287384	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17869398	GCAGCAGCTCCTCGG[C/T]GACCTCCTCATTGGA	146691
rs199905322	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17961023	GGGAGAAAATATTTG[C/T]AAATCACATGTCTGA	146691
rs199937944	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17906131	TTTGTCTTCTCTTTT[C/T]ATTTTTTTTTTTTTT	146691
rs199943147	snp	A/C/T	0.000247091	0.0111127	synonymous-codon, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17898596	GAGAATAGCACTCAC[A/C/T]GTTAATGCCAGCATC	146691
rs199957406	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17943874	AGAGCCCAAGGTCTA[C/G]CTGCCACAAACATAC	146691
rs200001748	snp	A/G	0.000265103	0.01151	intron-variant	TOM1L2	GRCh38.p7	17:17907443	GAGAGGGGGGCACAC[A/G]TACCCTTCCTCCGTC	146691
rs200066297	in-del	-/CCTGT			intron-variant	TOM1L2	GRCh38.p7	17:17911306	TCAGGCCTGCCCTGC[-/CCTGT]CCAGTCCAGCCCAGC	146691
rs200097417	snp	C/T	0.00716266	0.059414	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847596	TCCACGGGGTGCGAG[C/T]GGGGACCCGCCATCT	146691
rs200113859	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17896763	AAGTCCACAAATGAA[A/G]ACACAAGCAGAGAGC	146691
rs200120270	snp	C/T	8.23608e-05	0.00641667	missense, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17884726	CATATATGTGCACAA[C/T]GCCGGTGAGATCAGG	146691
rs200179098	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17970432	ATTTTAAAGGTGTAG[A/C]GCTTCCTATTATAAA	146691
rs200200260	snp	A/G			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17845308	TCCCTGCTGCCCCTG[A/G]GGCAGCCAGGCCTCT	146691
rs200208686	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17954330	TTTTTTTTTTTTTTT[G/T]TGATGGAGCTTCGCT	146691
rs200213659	snp	A/G	8.18599e-05	0.00639713	intron-variant	TOM1L2	GRCh38.p7	17:17866452	TGGCCATAAGCCCCA[A/G]AACCCTGGAGTCAGG	146691
rs200243623	snp	A/G	0.001403	0.0264486	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847747	TCGGGAACCATTTCA[A/G]CAGCTTTGGCTCTTT	146691
rs200296185	snp	A/C/T	0.000957326	0.0218577	intron-variant	TOM1L2	GRCh38.p7	17:17866272	GGAAGTAGGTAGGCC[A/C/T]TTTTGTCCCTGTGAG	146691
rs200447964	in-del	-/GCCT			intron-variant	TOM1L2	GRCh38.p7	17:17911295	ATTACCCGAGCTCAG[-/GCCT]GCCCTGCCCTGTCCA	146691
rs200460740	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17875286	AAAAAAAAAAAAAAG[C/T]ACAGAAGGTGAGAAG	146691
rs200485753	snp	A/C/G	3.30301e-05	0.00406377	intron-variant	TOM1L2	GRCh38.p7	17:17884590	CAGCTTGGCTCACCC[A/C/G]TTCTGCAGTAGGTCT	146691
rs200557620	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17848495	CCAAGGGTGCTGCTG[C/T]GCACCTCCACAAACT	146691
rs200566614	snp	G/T	0.00199806	0.0315443	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17848824	TGGCCAGGCCATACC[G/T]TCACTTGTGACACCC	146691
rs200600237	in-del	-/T	0.115788	0.21092	intron-variant	TOM1L2	GRCh38.p7	17:17920218	TTTATTCTCTCGTTC[-/T]TTTTTTTTTTAATTA	146691
rs200639065	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17855962	AATATTTGTTGTAAA[A/G]AAAAAAAAAAAAACA	146691
rs200653624	in-del	-/TTTTATTTTTAT			intron-variant	TOM1L2	GRCh38.p7	17:17854485	TCTGATGTGTCATAG[-/TTTTATTTTTAT]TTTTATTTATTTATT	146691
rs200695831	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17852500	ACTTTCAGAAAGGCC[G/T]AAGCCAGTCACTGAT	146691
rs200708706	in-del	-/CC	0.0150606	0.0854603	intron-variant	TOM1L2	GRCh38.p7	17:17920431	CCACAACCGCCGGCT[-/CC]CGGGTTCAAGCAATT	146691
rs200715176	snp	C/T	0.00199792	0.0315431	missense, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17882802	GAATAGGAACCAGCA[C/T]TTGTCCTCTGCTGTG	146691
rs200818129	in-del	-/T	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17873637	GGGAGCAGGGGTTGA[-/T]TGTCAGTCTCCTCAA	146691
rs200846712	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17956872	ACATCTCCCTGCAAG[C/G]TGAGGGAGGCGGCTC	146691
rs200859885	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17900296	AGGCCGAGATGGGTG[C/G]ATCACTTGAGGTCAG	146691
rs200865180	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17894934	AAACTCTGTCTCAAA[A/T]ACATACATACATACA	146691
rs200871331	snp	C/T	0.00199799	0.0315437	intron-variant	TOM1L2	GRCh38.p7	17:17893658	GCAAGGGGTCCAACC[C/T]ACCTGGATCAGAGCA	146691
rs200887854	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17952376	GTGCTTCTTTATTTT[C/T]TTTTTTTTTTTTTTT	146691
rs200890228	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17879407	GCATTTTATAATCAG[C/T]AAAAAAATGTTATTA	146691
rs200892708	in-del	-/G	0.0248432	0.108648	intron-variant	TOM1L2	GRCh38.p7	17:17852971	ATGTGGGTCCTCACT[-/G]GGGGGGATGGACGCA	146691
rs200934002	snp	A/G			intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17858237	CTACATTTTTTTTTT[A/G]TCTTTTCTAGTGGCA	146691
rs200960434	snp	C/T	0.0136067	0.0813524	intron-variant	TOM1L2	GRCh38.p7	17:17869334	AAAAAGAAATCCGGC[C/T]CCCACCTCTCGTATC	146691
rs200964866	snp	A/C/G	4.94442e-05	0.00497188	intron-variant	TOM1L2	GRCh38.p7	17:17850878	CACAGATGAAATAGA[A/C/G]AAGTCGAGTCTCACC	146691
rs200969782	in-del	-/ACAT			intron-variant	TOM1L2	GRCh38.p7	17:17894978	CATACATACATACAT[-/ACAT]GCATGCATGCATGCA	146691
rs200990292	snp	C/G	0.000192619	0.00981185	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847640	ACAGAGCTGCTCACA[C/G]GGCGAAGAGGGCATC	146691
rs200992928	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17955324	CCAGACCACACAATT[C/T]CTTTTTTTTTTTTTT	146691
rs200998156	snp	A/T	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17923530	CTCTACAAAAAAAAA[A/T]TTTTTTTTAATTAGC	146691
rs201002134	in-del	-/GTAA			intron-variant	TOM1L2	GRCh38.p7	17:17902944	AGGGAGATGAAGTAA[-/GTAA]CTCACACAGGCTCGC	146691
rs201006886	in-del	-/CT	0.0930568	0.194599	intron-variant	TOM1L2	GRCh38.p7	17:17886175	GCAGCCACAGAAACT[-/CT]GTCTCTAACCAACAG	146691
rs201070873	in-del	-/T	0.0189856	0.0955633	intron-variant	TOM1L2	GRCh38.p7	17:17915515	TTGGCCCCTCACCCC[-/T]TTTTTTTTAAGAGAC	146691
rs201125880	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17850544	CCCAACACTCCCTCC[C/T]CCAAAAAACCAAAGC	146691
rs201174884	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17852354	GTCCCAGGTAGAGTC[C/T]AGCACTCTGAGCAGG	146691
rs201178500	in-del	-/T	0.0166325	0.0896639	intron-variant	TOM1L2	GRCh38.p7	17:17868585	GGTCCTTTCTGGTCC[-/T]TATGCTGAGTCCTTC	146691
rs201189467	in-del	-/CT	0.0193772	0.0965046	intron-variant	TOM1L2	GRCh38.p7	17:17962355	GGATGGAGTCTCGCT[-/CT]GTCACCCAGGCTGGA	146691
rs201194960	snp	C/G	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17883029	CCCCACTGAGCCCAG[C/G]CTCTCCATCTGGGAA	146691
rs201202809	snp	A/C/G/T	0.000115335	0.00759319	synonymous-codon, intron-variant	TOM1L2	GRCh38.p7	17:17862817	TTGCTGGAGTGAACT[A/C/G/T]AGGGTGCCACTGACG	146691
rs201213109	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17945267	CACCACACACACACA[C/T]ACACACACACACACA	146691
rs201221655	snp	C/T	0.00315749	0.0396077	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	TOM1L2, DRC3	GRCh38.p7	17:17972359	CCCCTGTCTGCCACC[C/T]AGGCCTCCGCTGTAA	146691
rs201316492	snp	C/T	6.60873e-05	0.00574798	synonymous-codon, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17907455	CACGTACCCTTCCTC[C/T]GTCTCATTGATGATG	146691
rs201350393	in-del	-/T	0.0611083	0.163768	intron-variant	TOM1L2	GRCh38.p7	17:17921953	ACCAGCCTTTTTTTT[-/T]GAGCTTCTCCCGATG	146691
rs201460966	in-del	-/GC			intron-variant	TOM1L2	GRCh38.p7	17:17852117	ATTACAAAAATGCCA[-/GC]TCTGTCTATAGCTGG	146691
rs201467144	in-del	-/T	0.030665	0.119967	upstream-variant-2KB, intron-variant	TOM1L2, DRC3	GRCh38.p7	17:17973610	CTTTTTTAAGAAAAA[-/T]TTTTGTTCATTATTT	146691
rs201470533	snp	A/G			upstream-variant-2KB, intron-variant	TOM1L2, DRC3	GRCh38.p7	17:17974012	TATAAGATCCCCATA[A/G]AAGAGGACTGTTTGG	146691
rs201500161	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17946278	ATTAGTACATATATT[C/T]ACAGAGTTGTGCAAC	146691
rs201589396	snp	C/G	1.65239e-05	0.00287431	intron-variant	TOM1L2	GRCh38.p7	17:17884588	AGCAGCTTGGCTCAC[C/G]CGTTCTGCAGTAGGT	146691
rs201598372	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17947838	AACAAGTTGTATTCA[C/T]TTTTAATTTCTTTTG	146691
rs201662293	snp	C/G	4.95152e-05	0.00497545	intron-variant	TOM1L2	GRCh38.p7	17:17884601	ACCCGTTCTGCAGTA[C/G]GTCTTTCTAGAAAGT	146691
rs201716163	snp	A/G	0.000444682	0.0149045	synonymous-codon, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17898635	GTAGTTCCGGTTCCC[A/G]TTGAGCCGCTTCTTC	146691
rs201756024	in-del	-/AG	0.0130921	0.0798413	intron-variant	TOM1L2	GRCh38.p7	17:17927098	AGATCAAAATCCAAC[-/AG]GGAATAGGCATTTTC	146691
rs201811747	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17958189	GTTCAACCTCTGTTC[C/T]TCAAAACAAACGAAC	146691
rs201832403	snp	C/T	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17895882	ACCATGTAACTTAAC[C/T]TAGGAGGCCAAAGCT	146691
rs201841501	in-del	-/C			intron-variant	TOM1L2	GRCh38.p7	17:17962231	GTAAAATGGTAGTTG[-/C]CAGGGGCTGGGGGGA	146691
rs201848045	in-del	-/TC			intron-variant	TOM1L2	GRCh38.p7	17:17969881	CTCTCTCTCTCTCTC[-/TC]AGAAGACTGACAAAC	146691
rs201857256	in-del	-/AAAAAAAA			intron-variant	TOM1L2	GRCh38.p7	17:17885925	GCAAGACTCCGTCTC[-/AAAAAAAA]AAAAAAAAAAAAAAA	146691
rs201901656	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17926261	TCTGAACATACAGAC[C/T]TAAGGATAAAAGCCT	146691
rs202004431	snp	A/G	4.94271e-05	0.00497102	synonymous-codon, upstream-variant-2KB, intron-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17862787	AAACATGTCAAAGCC[A/G]TCACGGGGATTACAT	146691
rs202014353	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17969465	TTAAAAGAATACTAA[C/G]AACACTAAATATCAA	146691
rs202027819	in-del	-/TC	0.021333	0.101051	intron-variant	TOM1L2	GRCh38.p7	17:17916139	AGTGCAGTGGCGCGA[-/TC]TCAGCTCACTGCAAG	146691
rs202028070	in-del	-/G			intron-variant	TOM1L2	GRCh38.p7	17:17938763	AGGCAAAGGTTGAAA[-/G]GGGTTTTTTTTTTTT	146691
rs202079010	snp	G/T	0.00137507	0.0261848	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847700	AAGGGTTTGAGGCTG[G/T]GGCAGGAGCCTCCAT	146691
rs202095814	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17902821	TGAAGATACAGTTAT[A/G]TAGCCAGATACATCA	146691
rs202104443	in-del	-/T	0.0166325	0.0896639	intron-variant	TOM1L2	GRCh38.p7	17:17868588	CCTTTCTGGTCCTTA[-/T]GCTGAGTCCTTCATG	146691
rs202127899	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17945273	ACACACACATACACA[C/T]ACACACACACACACA	146691
rs202176189	snp	A/G/T	3.62807e-05	0.00425902	intron-variant	TOM1L2	GRCh38.p7	17:17907581	TCCTGGAATAAGTGG[A/G/T]CCTTGGCAGGAAATG	146691
rs202242757	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17946279	TTAGTACATATATTC[A/T]CAGAGTTGTGCAACC	146691
rs367643455	snp	G/T	0.0023933	0.0345097	intron-variant	TOM1L2	GRCh38.p7	17:17886977	CATGTGCCAGCACAG[G/T]ACTGGAAGCAGAGAC	146691
rs367652676	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17910785	CGTTGGCCAGACTGG[A/T]CTCGAACTCCTGACC	146691
rs367692512	snp	C/G	0.000153988	0.00877328	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17862703	CCCCCAATATCTTTA[C/G]AGAGCCACTAAAAGG	146691
rs367787859	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17851776	AAAGAAACCAAGTTC[A/G]GCTGAGCACTGGGGC	146691
rs367792902	snp	A/G	0.00438332	0.0466095	intron-variant	TOM1L2	GRCh38.p7	17:17874042	CTCACTGCAAGCTCC[A/G]CCTCCCGGGTTCATG	146691
rs367833252	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17941370	CCTCGGATGACTATG[A/G]ACGACTCCCTTATAT	146691
rs367888650	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17871506	AAAACCCCATCTCTA[C/T]GAAAAAATACAAAAA	146691
rs367907915	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17964633	CACAGTGGCTGAAAC[C/G]TATAATCCCAGCACT	146691
rs367914908	snp	C/T	1.64885e-05	0.00287123	intron-variant	TOM1L2	GRCh38.p7	17:17884787	GGATAATAGAAGGCC[C/T]GTTAGGAAGCATTTC	146691
rs367931506	snp	C/T			intron-variant, upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17971890	GTGCCCGGGAGGAGG[C/T]CCGAGGACACAGATG	146691
rs367962637	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17917124	GAGATCACGCCACTG[C/T]ACTCCAGCCTGGGAG	146691
rs367974603	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17957754	ACACACACACACGTA[C/T]ACACACATATGATTC	146691
rs367991496	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17938274	GAGGTATACAAGTCT[A/G]GGCGGGTAGCCACCT	146691
rs368013634	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17943859	CCCACGTGAACATCC[A/G]GAGCCCAAGGTCTAG	146691
rs368043815	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17930744	GCTGAAAACCAAATG[A/G]AATAAAAGAAGAAAT	146691
rs368089054	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17920427	CTCACCACAACCGCC[A/G]GCTCCCGGGTTCAAG	146691
rs368135913	snp	A/C	0.000182051	0.009539	intron-variant	TOM1L2	GRCh38.p7	17:17882686	CTGGCTTGCCTATGG[A/C]CCCGAAGTATGCAAG	146691
rs368173617	snp	C/T	0.000101261	0.00711478	intron-variant	TOM1L2	GRCh38.p7	17:17893639	CTCTGTTCCAACAAA[C/T]TGGGCAAGGGGTCCA	146691
rs368229418	snp	A/T	0.0383715	0.133092	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17846327	GCATACAGCTGCAGT[A/T]TTCTCCTTCTGAGCA	146691
rs368237067	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17928439	AACAGGCAGGATAAA[A/T]TATTATGTGCATACT	146691
rs368237767	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17866081	ATTTCCCCCATCCCT[A/G]CTTTCCAACATAGAT	146691
rs368246255	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17968804	CACAGATGTGCCTGT[A/G]CCCCACTCCCTGCCT	146691
rs368290783	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17929881	TATGAACACTTAGAC[A/G]AGTTAAACACAACAT	146691
rs368309703	snp	A/T	1.6473e-05	0.00286988	missense, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17884684	AGTCTGCCATGGGAA[A/T]TTCAACCCCTTTCCT	146691
rs368358107	snp	C/T			intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17859771	CTGTAATACCAGCTA[C/T]TCAGGAGGCTGAGGC	146691
rs368367418	in-del	-/T	0.00103946	0.0227739	intron-variant, splice-donor-variant	TOM1L2	GRCh38.p7	17:17893658	CAAGGGGTCCAACCT[-/T]ACCTGGATCAGAGCA	146691
rs368373845	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17901453	TCTGGGCCATGATCA[G/T]GCTCCTCAAAGTCTC	146691
rs368469555	snp	C/G/T	9.93012e-05	0.00704575	synonymous-codon, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847716	GGCAGGAGCCTCCAT[C/G/T]GGGGGCGAGGGGAGG	146691
rs368497617	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17921563	AAGGCCTCTGCAGGA[G/T]CCAGCCAGGCCCCAA	146691
rs368508954	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17849740	ACCTGCTATGTAGCC[C/T]TACTGGACACATCCC	146691
rs368530167	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17970009	GCTCTTTCCACTTGC[A/T]ATATATCCCTATATC	146691
rs368534395	snp	A/G			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17845103	AGTGGAACCCACTCT[A/G]GGGCACCGGGGCTAT	146691
rs368535621	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17925833	GTACTCTAGCCTGGG[A/T]GACACAGTGAGACCC	146691
rs368553102	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17915530	CTTTTTTTTAAGAGA[A/C]AGGATCTCACTTTGT	146691
rs368557607	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17940529	AGAGTCCTGTGGGTG[C/T]AGAGCATGGAGAAGT	146691
rs368561210	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17959167	TGGGGAAGGCATCAC[A/G]GGAATCCCCAATTTA	146691
rs368657965	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17935755	TAGGACATAAGGAAC[A/G]AGGTCACAAGTGATG	146691
rs368658342	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17875261	ACTCCTTCTCAAAAA[A/G]AAAAAAAGAAAAAAA	146691
rs368670982	snp	A/C/G	5.07055e-05	0.00503494	intron-variant	TOM1L2	GRCh38.p7	17:17893820	CAGCACCTGATGTGG[A/C/G]GAGGGAAGGAAAAGG	146691
rs368711763	snp	A/G			synonymous-codon, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17884733	GTGCACAACGCCGGT[A/G]AGATCAGGACTGCTT	146691
rs368745364	snp	C/T	0.0023933	0.0345097	intron-variant	TOM1L2	GRCh38.p7	17:17906285	AGGTGTGCACCACCA[C/T]GCCTGGCTAACTTTT	146691
rs368760571	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17863464	GGTTTGGAGGCCAGG[A/G]TGTGTGAAGTGAACA	146691
rs368777753	snp	A/G	3.30371e-05	0.00406417	intron-variant	TOM1L2	GRCh38.p7	17:17848794	AGAGGCAACAAAAGG[A/G]GGCTGTAAGGCCACT	146691
rs368797073	snp	A/G	1.64959e-05	0.00287188	intron-variant	TOM1L2	GRCh38.p7	17:17884611	CAGTAGGTCTTTCTA[A/G]AAAGTGCCAGCTGGA	146691
rs368798310	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17966537	CCAAACCTACTGAAA[C/T]AGAAACTCTGAGGGT	146691
rs368850260	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17854297	GCGCTCCTTGTCAGG[C/G]TGATGGGAGGGAAGT	146691
rs368984208	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17962910	AGGTTGCAATGAGCC[C/G]AGGTCGTGCCACTGC	146691
rs369013597	snp	C/G	0.000148688	0.00862101	synonymous-codon, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17869426	GGACACGCGGGAGAT[C/G]AGCTCCACGATGCGC	146691
rs369066421	snp	G/T	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17881152	ACCAGGGAGATGGTC[G/T]GGGTCCTGAGAGGCT	146691
rs369069269	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17930034	GCCTGGGCACACACA[A/G]GAAGGCAAGAGCACC	146691
rs369075728	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17951526	AACAGAAAAATTTGG[C/T]TTCCTCAGGAGTAGC	146691
rs369090044	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17902974	CACAATAAGCGAGTG[A/G]TGACCTAGAATTGCT	146691
rs369098448	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17873842	CGGCCTCCATGGCAC[A/G]GGGCCAGGGCAGCTG	146691
rs369110926	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17948485	AACCCCGTCTCTACT[A/G]AAAATACAAAACAAA	146691
rs369126280	snp	G/T	0.0023933	0.0345097	intron-variant	TOM1L2	GRCh38.p7	17:17961733	AAAAATTAGCCGGGC[G/T]TGGTGGCAGGCGCCT	146691
rs369129462	snp	A/G	8.24056e-05	0.00641841	intron-variant	TOM1L2	GRCh38.p7	17:17850884	TGAAATAGAAAAGTC[A/G]AGTCTCACCAGGTCG	146691
rs369187930	snp	A/C	0.000145057	0.00851514	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17866365	TTGGGCTCACCACGG[A/C]TGGAGACCCTGGCCC	146691
rs369244199	in-del	-/ATT			intron-variant	TOM1L2	GRCh38.p7	17:17937290	TTCTACTGTAATCCT[-/ATT]CAAGGAACACCGACA	146691
rs369253025	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17865262	TCCAAGCCCTCTGTA[A/G]ATATTGACAATCAAT	146691
rs369287558	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17951914	AGGCAAACAGTCACT[C/T]GGGCTCTGTTGGTGA	146691
rs369297606	snp	A/C/T			intron-variant	TOM1L2	GRCh38.p7	17:17871226	ACACAAAAAATTAGC[A/C/T]GGGCGTTGGTGGCGG	146691
rs369309745	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17897814	ATCATCTGTACGGGG[A/G]AGGATAGTAAAATCT	146691
rs369310259	snp	C/G/T	9.9189e-05	0.00704171	synonymous-codon, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17869378	GTTGAGGTCATCGTT[C/G/T]ACATGCAGCAGCTCC	146691
rs369336762	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17908171	ATTATTTTATCTCAT[C/T]CACAAAATGACTTTC	146691
rs369474704	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17945044	ATGGAAATGTAGGAT[C/T]TCCCATTAATCAGGG	146691
rs369528742	snp	A/G	0.00716266	0.059414	intron-variant	TOM1L2	GRCh38.p7	17:17963139	GGTGCAAGTGTTCTT[A/G]TACTCCCTTCACCAC	146691
rs369606512	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17900257	CAGCATTATGGCTCA[A/T]TCCTGTAATCCCAGG	146691
rs369632310	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17967169	GGTTAAACGTCTACC[A/G]TTCACAGGATATTAT	146691
rs369750846	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17897143	GTTGGGTGTGTAAAT[A/G]GAGATGTTTTAGATA	146691
rs369760871	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17867170	GTGGCTGGCCCATCA[C/T]GGAGGTCATTGTGAG	146691
rs369767690	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17923896	TAATCTCAGCACTTT[A/G]GGAGGTCGAGGTGGG	146691
rs369770321	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17917193	AAAAATTAGCTGGGC[A/G]TGGTGGCGCACACCT	146691
rs369774049	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17883139	AGCACCGAGAGTGCT[C/G]TGTGAGCCCTCTGGT	146691
rs369794952	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17872552	AAAAGGGAGGCTGGG[C/T]AGTAGGACAGAGAAA	146691
rs369867440	snp	A/C			intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17859500	ATATGTGTAGACACA[A/C]ACAGACACACACAGC	146691
rs369916789	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17891837	AGAGGGAGACAGAGA[A/G]ACAGAAGGATATTGG	146691
rs369926682	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17916748	TTGTTTAGGGCCAGG[C/T]GCAGTGGCTCACGCC	146691
rs369929552	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17864580	GCAGTGGCACAATCT[C/T]GGCTCACTGCAACCT	146691
rs369932741	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17938107	CTCCCTCTCACCCAG[C/T]GTGGTGCAATGGGAA	146691
rs369947230	in-del	-/A			intron-variant	TOM1L2	GRCh38.p7	17:17903612	GCGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA	146691
rs369970593	in-del	-/ACAC			intron-variant	TOM1L2	GRCh38.p7	17:17945268	ACCACACACACACAT[-/ACAC]ACACACACACACACA	146691
rs369975685	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17890278	TGGTGGCTGAGAACA[C/G]CCAAGAGCCCAGTGG	146691
rs369984263	snp	C/T	1.64969e-05	0.00287196	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17879716	TGTTTCCTCGAACGA[C/T]GTCCAGTTCACTCCG	146691
rs369986925	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17938619	CAGATTCCACTTCTA[C/T]CCACATACTCATAAA	146691
rs369994414	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17882472	TGCCTCCCAGGCACC[A/T]CTCAACCCTGGGCTC	146691
rs370048714	snp	C/T	1.6483e-05	0.00287076	synonymous-codon, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17850938	GTCCATGACAGATGG[C/T]TGCGCAACGGGGATC	146691
rs370051264	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17884030	CTTTTAACCCTGAAG[C/T]GCCAAGCTGCCCCCT	146691
rs370128787	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17952672	AGTGCTGGGATTACA[A/G]GTGTGAGCCACCACA	146691
rs370170703	snp	C/T	7.03284e-05	0.00592953	synonymous-codon, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847638	CCACAGAGCTGCTCA[C/T]AGGGCGAAGAGGGCA	146691
rs370279147	snp	A/G	3.29582e-05	0.00405931	missense, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17882775	GCGGAGTAGGGAGCA[A/G]GAGGCGGCGAGGAAT	146691
rs370314804	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17922898	AAGTGGCCACCTTAA[C/G]TGCCTCCTGGAGTGT	146691
rs370375492	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17892261	CACCTGACCCATCTG[A/G]GAGCCCGGCCTGCCC	146691
rs370392640	snp	C/G	0.0023933	0.0345097	intron-variant	TOM1L2	GRCh38.p7	17:17884069	CTCAAGTTACTGTTG[C/G]CACTGCAAAAGCTTT	146691
rs370402084	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17909969	AGGAGTTTGAGGCTG[C/T]AGTGAGATATGATTG	146691
rs370406124	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17953659	GACCTCACTGACCTG[C/T]CCCCACCAGCCCAAC	146691
rs370443913	in-del	-/G			intron-variant	TOM1L2	GRCh38.p7	17:17955250	GCAGACAATATGGTG[-/G]TCACCGGCAGAGGGC	146691
rs370444624	snp	A/G	3.62707e-05	0.0042584	intron-variant	TOM1L2	GRCh38.p7	17:17866434	CCTGTCAGAACATGA[A/G]ATTGGCCATAAGCCC	146691
rs370447300	in-del	-/TAAA			intron-variant	TOM1L2	GRCh38.p7	17:17902194	AAATAAATAAATAAA[-/TAAA]AACAGTCCCAGGTAG	146691
rs370496202	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17898379	CCTTATCTTCTGCTC[C/G]TATACATTTACCAAA	146691
rs370509140	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17920883	TCAGGTGATCCACCC[A/G]CCTCAGCCTTCAAAG	146691
rs370564768	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17944990	GCAGATGCTGCCCGC[A/G]CTGCCGCCGCCACAC	146691
rs370578073	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17878533	TTTGGAGTAGGAAGG[A/G]GGCACAATAAGCAGC	146691
rs370581016	snp	A/G	0.000216196	0.0103948	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17862694	GGGTCAATCCCCCCA[A/G]TATCTTTAGAGAGCC	146691
rs370603083	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17925135	CAGAAGCAGCTGCCA[A/G]TACTATGCTTCCTAT	146691
rs370606144	snp	C/T	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17888369	AACATAAACCATAAC[C/T]TATTCATTTCTGTAT	146691
rs370628988	snp	A/G	0.000153988	0.00877328	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847723	GCCTCCATGGGGGGC[A/G]AGGGGAGGTCGGGAA	146691
rs370686384	snp	A/G	0.00358779	0.0422022	intron-variant	TOM1L2	GRCh38.p7	17:17902632	CAGGGCCTGCAGGGC[A/G]TGGCACATGCCAAGT	146691
rs370788824	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17913399	CCATGGAGCAGATGC[C/T]GGGCCATCCTGCCCC	146691
rs370796784	in-del	-/CT	0.0023933	0.0345097	intron-variant	TOM1L2	GRCh38.p7	17:17875657	ACCTTGGTAAATATC[-/CT]CTTTTTTCTATCTAA	146691
rs370835723	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17915037	GTGTGAGTTCTATCT[A/C]GTTTGTTACGTAAAA	146691
rs370871324	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17867844	CGACTTGTGTGTTTT[C/T]TCAACAGTGGTCTAC	146691
rs370884264	in-del	-/CATA			intron-variant	TOM1L2	GRCh38.p7	17:17894972	atacatacatacata[-/CATA]catgcatgcatgcat	146691
rs370887219	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17903340	CAAAATGTTGAGTAA[C/T]TGGCTGGGCGCGGTG	146691
rs370908256	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17958819	CAAGGTACATTTCAG[C/T]GTTGGAACTTTTAGC	146691
rs371012675	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17963827	GATAAATAACAACAG[A/T]AACAGTGGAGGGAAG	146691
rs371034710	in-del	-/AAAT			intron-variant	TOM1L2	GRCh38.p7	17:17964759	ACCCTGTCTCAAAAA[-/AAAT]AAATAAATAAAAAGC	146691
rs371043869	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17959401	TGTCAGAAATGTCAT[A/C]CATCACAGACACCCT	146691
rs371043896	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17940716	CACAGCTGTCATTGG[G/T]GTGACCTCGCTAATT	146691
rs371094169	snp	C/T			upstream-variant-2KB, intron-variant	TOM1L2, DRC3	GRCh38.p7	17:17974062	GACAACTGTGAGAAA[C/T]ACTGTGAGCTGTGGC	146691
rs371116987	snp	A/G	0.000159987	0.00894248	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	TOM1L2, DRC3	GRCh38.p7	17:17972263	ACACGCGGCCTTACC[A/G]AGGCACTGCCCCACT	146691
rs371153984	snp	A/G	0.000875616	0.0209055	intron-variant	TOM1L2	GRCh38.p7	17:17866822	TCCAGCCTCCAAAAC[A/G]TGGAGGGGTAGGTCT	146691
rs371170595	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17864880	TCTGATACAGAAATA[C/G]TGGCTACAAATATAC	146691
rs371180188	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17957067	CGCTGCAGTCTCCAC[A/C]TCCTGGGCTCAAGCA	146691
rs371189715	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17929546	CGAGGCAGGAGAATC[A/G]CTTGAACCCGGGAAG	146691
rs371214368	snp	A/G/T	0.000296897	0.0121803	intron-variant	TOM1L2	GRCh38.p7	17:17850973	GAGGCGGCAAGCAGC[A/G/T]GGCCAGGCAGCCCCC	146691
rs371220435	snp	A/G/T			intron-variant	TOM1L2	GRCh38.p7	17:17955889	GCTGCAGACCTTCGC[A/G/T]GTGAGTGTTACAGCT	146691
rs371248512	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17897988	TGGAGTGCAGTGGTG[C/T]GATCTCAGCTCACGG	146691
rs371255833	snp	C/T			intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17859185	GGTTCAAGCGATTCT[C/T]CTACCCCAGCCTCCT	146691
rs371317539	snp	A/C/T			intron-variant	TOM1L2	GRCh38.p7	17:17882253	CACAACTCAGCTGCA[A/C/T]GTCTATGCTTTTGGC	146691
rs371318310	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17851790	CAGCTGAGCACTGGG[G/T]CGCAGCAGCCAGAGC	146691
rs371419866	snp	C/T			intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17860787	ACACACATTCTTTCC[C/T]CTTCAGTAATCCGAA	146691
rs371436530	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17887397	GGTGTCTCTCATCTC[G/T]GGGTGTCTCCCATTC	146691
rs371446968	snp	C/T	1.65051e-05	0.00287267	intron-variant	TOM1L2	GRCh38.p7	17:17884815	TTCTCAGAGCTGCCA[C/T]GGTATCTGAAAATCC	146691
rs371455911	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17864500	CAGGCGTTAGCCACC[A/G]CACCCGGCTTTTTTT	146691
rs371456416	snp	A/C/T	0.000133344	0.00816422	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847678	CGCTCTGGCTTCTTC[A/C/T]GGCCAGAAGGGTTTG	146691
rs371512082	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17967731	TTCCGCCTCAGCCTC[C/T]CGAGTAGCTGGGATT	146691
rs371519640	in-del	-/G	0.0150606	0.0854603	intron-variant	TOM1L2	GRCh38.p7	17:17893387	CCAAGTTTTCTCAGA[-/G]GCCTGTTGAGGCCAC	146691
rs371535609	snp	A/G	6.64684e-05	0.00576453	intron-variant, missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17893780	GGATGTGGAAGCGGT[A/G]GCCACAGTTCTTCAC	146691
rs371549893	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17876947	ACCAACTTCCTGGAA[A/G]GTCTCTCCCAACTCA	146691
rs371612900	snp	C/G	1.65236e-05	0.00287429	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17869390	GTTCACATGCAGCAG[C/G]TCCTCGGTGACCTCC	146691
rs371614278	snp	C/T	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17971937	GATAGCACCGGCACC[C/T]GGCGAAGGCCCAGCC	146691
rs371634438	in-del	-/T	0.353587	0.22753	intron-variant	TOM1L2	GRCh38.p7	17:17864212	CAGAATCCAATTTGA[-/T]TTTTTTTTTTTTTTT	146691
rs371659569	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17920651	CTTTTTTTCTTTTTC[G/T]TGAGACGGAGTATCA	146691
rs371693801	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17895868	TGAGGATCAGAGGTA[C/T]CATGTAACTTAACCT	146691
rs371703938	snp	A/G	0.00478085	0.0486577	intron-variant	TOM1L2	GRCh38.p7	17:17902416	AATACAAGAAGTGCA[A/G]GCAGCACTTCAGTGG	146691
rs371718506	snp	C/T			intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17862306	GCTATCAGAGGAGCC[C/T]CTGCTCTGACCACTT	146691
rs371720565	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17911980	TTGGGGGTAAGGTCA[C/T]AGATCAACAGGATCC	146691
rs371740816	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17874080	CCTGCCTCAGCCTTC[C/T]GAGTAGCTGGGATTA	146691
rs371792623	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17917687	AGCTTCCCAGGCCAG[C/G]TCATGCCTGTAAATC	146691
rs371800783	snp	A/G	4.94931e-05	0.00497434	intron-variant	TOM1L2	GRCh38.p7	17:17848882	AGGAGCAGAGAAAAT[A/G]AAATTAGGGCACTGG	146691
rs371810816	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17889515	CCACCATCCTCAGGG[A/C]AACCAAAGGGGCAGT	146691
rs371818533	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17956315	GATACAGAGTGCTGA[C/T]TGGTGCATTTACAAA	146691
rs371911723	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17962016	AATGTGGTATAAACA[A/C]ACAATGGAATATTAT	146691
rs372066308	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17872040	CTGCCTGGGCCTTGG[A/G]GCCTGCCAGACGTGG	146691
rs372084016	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17946926	AATGGAGTTTTACCA[C/T]GTTGGCCAGGCTGGT	146691
rs372085622	snp	A/G	0.00438332	0.0466095	intron-variant	TOM1L2	GRCh38.p7	17:17965281	CTACTTAGCCAACAT[A/G]TGAAGCAAGCCCTCC	146691
rs372105318	snp	A/G	0.000101673	0.00712923	intron-variant	TOM1L2	GRCh38.p7	17:17893824	ACCTGATGTGGGGAG[A/G]GAAGGAAAAGGGTCA	146691
rs372136305	snp	C/G	3.37143e-05	0.00410561	intron-variant	TOM1L2	GRCh38.p7	17:17893642	TGTTCCAACAAATTG[C/G]GCAAGGGGTCCAACC	146691
rs372208672	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17886307	ACTTATTTAATTTGC[A/G]TGCTCAGGGATTTAA	146691
rs372229292	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17880785	ATGCGGCGCCTGGCA[C/T]GCAGGTATGCTCTCT	146691
rs372249343	in-del	-/TGGAG			intron-variant	TOM1L2	GRCh38.p7	17:17851511	TGGTGCATTTCTGAG[-/TGGAG]AGGGGAACTGGAGGA	146691
rs372265719	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17896419	CAGAGCAACAGTGGC[A/G]GGAACCACTGCCCGC	146691
rs372271762	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17950639	AGGATCCTGCTAGAA[C/G]AATCTTGCTTTGATT	146691
rs372274309	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17969160	CTCCCAGGTTCAAGC[A/G]ATTCTCCTGTCTCAG	146691
rs372278346	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17941877	CACCTATAGTCCCTG[C/T]TACTAGGGAGGGAAG	146691
rs372280905	in-del	-/C	0.00279162	0.0372561	intron-variant	TOM1L2	GRCh38.p7	17:17883558	GCTAACACAATGAAA[-/C]CCTGTCTCTACTAAA	146691
rs372299180	snp	A/C/T	7.51673e-05	0.00613015	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847585	AGTGCCCGGTGTCCA[A/C/T]GGGGTGCGAGCGGGG	146691
rs372310496	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17906375	CTCAAGCAACTGGCC[C/T]ACCTTGGCCTCCCAA	146691
rs372332711	snp	C/T	0.00318978	0.0398085	intron-variant	TOM1L2	GRCh38.p7	17:17950889	AACCTAGGCCAGAGC[C/T]TTGGTGCAGAGGGAA	146691
rs372356587	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17916749	TGTTTAGGGCCAGGC[A/G]CAGTGGCTCACGCCT	146691
rs372390020	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17907131	GGAGGAGGGGAGGGA[C/T]GAGGTGACACTTGGG	146691
rs372423345	snp	G/T	4.96775e-05	0.0049836	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17862720	GAGCCACTAAAAGGG[G/T]CCCCACATACGTCTT	146691
rs372446417	snp	A/G	0.000139894	0.00836227	synonymous-codon, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847641	CAGAGCTGCTCACAG[A/G]GCGAAGAGGGCATCC	146691
rs372470867	snp	A/G	0.000153988	0.00877328	stop-gained, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17866917	GGCCAGACCTGTATC[A/G]TTCGAACCTAACAGG	146691
rs372488953	snp	C/T	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17905635	CCTCGAACTCCTAGG[C/T]GTAAGCAATCTTCCT	146691
rs372509876	in-del	-/TGTTT			intron-variant	TOM1L2	GRCh38.p7	17:17934589	TGTTTTGTTTTGTTT[-/TGTTT]AGGGGGATAATTTCT	146691
rs372567375	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17914239	AGGCTCCCAGCACAC[C/G]TGGGGCTCATTCTGT	146691
rs372623468	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17918706	CACAAGAGAGGCCCT[A/C]TGATGGGCTCCAGCA	146691
rs372626043	snp	A/G	3.2962e-05	0.00405954	missense, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17850907	CCAGGTCGGTCCTGA[A/G]CCACACCTCAATGTC	146691
rs372667099	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17965803	TCTGGCACATAGGAA[C/T]ACAACATTAAACTTT	146691
rs372780272	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17873216	AAAATTTTCAAACAT[A/G]CAGCAAAACAGGAAG	146691
rs372811565	in-del	-/T/TT	0.464096	0.129085	intron-variant	TOM1L2	GRCh38.p7	17:17938766	CAAAGGTTGAAAGGG[-/T/TT]TTTTTTTTTTTTTTT	146691
rs372812461	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17898002	GCGATCTCAGCTCAC[A/G]GCAACCTCCACCTCC	146691
rs372830327	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17970095	AGTCTCACTCTGTCG[A/C]CCAGGCTGGAGTGCA	146691
rs372864966	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17851311	CTAACTTCAGGAAGG[C/T]GCTGCCACGCAGGCT	146691
rs372875246	snp	C/T	0.00636936	0.0560724	intron-variant	TOM1L2	GRCh38.p7	17:17903080	TCCAGTCTGGTGTCA[C/T]TTCCTCCAAGAAGGC	146691
rs372942406	snp	A/G	0.000307953	0.0124049	intron-variant	TOM1L2	GRCh38.p7	17:17869497	CACATGCACCTCTGG[A/G]TAGCCTGCTGGGTGT	146691
rs372961286	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17966517	GTAGAATGCTACTTC[C/T]CACCCCAAACCTACT	146691
rs372982501	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17914148	GTCATTCCCTCTGGG[C/T]GTGGACAGAGGAGGG	146691
rs372993437	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17938911	CTTTCTATACACTGG[A/G]GTGGGGCCGCCCAGA	146691
rs372997791	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17945058	TTTCCCATTAATCAG[A/G]GCCGTGGACACCAAA	146691
rs372997989	snp	A/G	0.0422008	0.138995	intron-variant	TOM1L2	GRCh38.p7	17:17963535	TCTATTTCTTCACCT[A/G]TAAGATGAAGATAAC	146691
rs373063534	snp	G/T	0.000437904	0.0147905	intron-variant	TOM1L2	GRCh38.p7	17:17898540	TGTGAGGGGGGCAAG[G/T]CCAGGAGCAAGGAGT	146691
rs373072319	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17930920	CCTCTAGGATGGGGA[C/T]TTTTTTTCCCTAACA	146691
rs373106495	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17854601	GCGATCTCAGCTCAC[G/T]GCGACCTCTGCTTCC	146691
rs373175834	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17956292	CCAAGTCCCCACCAG[A/T]TTAACTAGATACAGA	146691
rs373277531	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17916974	CATCCTGGCCAACCA[A/G]CATGGTGAAACCCCA	146691
rs373286605	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17969535	TACATTAGAACCTAA[C/T]TCTGTCCATTAATCA	146691
rs373309082	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17962831	CTGGGCGTGGTGGCG[C/T]GTGCCTGTAGTCCCA	146691
rs373317024	snp	G/T			upstream-variant-2KB, intron-variant	TOM1L2, DRC3	GRCh38.p7	17:17973235	CAGGGCCAGAATGGA[G/T]TTTTAAGGGGTTCCG	146691
rs373358011	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17851431	CTCAGAGGGCAGGGC[A/G]GCACCAGCCCCGGGG	146691
rs373374421	in-del	-/GGCTCACTG			intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17858660	GATCTTGGCTCACTG[-/GGCTCACTG]CAACCTCTACCTCCT	146691
rs373434785	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17865359	CCAAAGAGCTGAAAC[C/T]TATCTGCCCTCCTTG	146691
rs373442514	in-del	-/C			intron-variant	TOM1L2	GRCh38.p7	17:17873667	ACAGAGCCCTAGCCC[-/C]AGCTGGGTGCTGGGG	146691
rs373471705	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17892519	CTCAGAGCCCTTCGA[A/T]GTCTTCCCACTGCCT	146691
rs373507323	in-del	-/G			intron-variant	TOM1L2	GRCh38.p7	17:17938772	TTGAAAGGGTTTTTT[-/G]TTTTTTTTTAATATT	146691
rs373526882	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17872615	GCCATGGACTGTTCC[A/G]GGCCACCGTGCGGGT	146691
rs373559844	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17895177	CTGGGAGTGCTCTGA[A/C]CTTCCCAGCACTGTG	146691
rs373561250	snp	C/G	0.00159617	0.0282053	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17845424	GGGGGCTCCCCAGGA[C/G]GGCGCCTATTTCAGC	146691
rs373565174	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17951963	AATTTGGCAGTCTCC[A/G]TCAAAATTTCCAATA	146691
rs373589806	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17906373	GGCTCAAGCAACTGG[C/T]CCACCTTGGCCTCCC	146691
rs373605111	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17940655	TCAGCAATGCCATTC[C/T]GATGAAGTTCAAGGC	146691
rs373612250	snp	A/G	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17927941	TATACTTTTAAAAAG[A/G]TTCCTTATCTTTTAG	146691
rs373621717	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17960183	TAGATTTTTCAGCTA[C/T]CAAGTTCATTCAGGC	146691
rs373623872	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17941082	CCCAGAACAGAGCTA[C/T]TGGAGACCATTTCTC	146691
rs373730677	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17899654	CAAAGCCCCTGTGCT[A/G]ACCTGACCCATCACC	146691
rs373788209	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17904982	TTCACCTTGGCATCC[C/T]GTAGCTGCTATACCT	146691
rs373811909	snp	A/G	3.30115e-05	0.00406259	intron-variant	TOM1L2	GRCh38.p7	17:17882697	ATGGCCCCGAAGTAT[A/G]CAAGTACCTGTTCTG	146691
rs373827216	in-del	-/TA			intron-variant	TOM1L2	GRCh38.p7	17:17868586	GTCCTTTCTGGTCCT[-/TA]TGCTGAGTCCTTCAT	146691
rs373861149	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17925965	CACTTGAGCCCAGGA[A/G]TTCAAAACCAGCCTG	146691
rs373890822	snp	A/G	9.89234e-05	0.0070322	intron-variant	TOM1L2	GRCh38.p7	17:17850958	CAACGGGGATCTATG[A/G]AGGCGGCAAGCAGCG	146691
rs373936757	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17897644	TGTTCCTTCCTGAAA[A/C]AAATCACTTGGCTGA	146691
rs373999990	in-del	-/A			intron-variant	TOM1L2	GRCh38.p7	17:17954866	GAAAACAAACAAAAA[-/A]CTCTCACACAGATAC	146691
rs374075561	snp	C/T	0.00126645	0.0251321	intron-variant	TOM1L2	GRCh38.p7	17:17907560	GAGAAAATGGGTTTA[C/T]ATTTCTCCTGGAATA	146691
rs374089226	snp	G/T	0.00716266	0.059414	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	TOM1L2, DRC3	GRCh38.p7	17:17972940	GGGAGACGCGTCTGC[G/T]GCGTGGAACCGCCGA	146691
rs374101464	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17864157	TACAGGCGTGAGCCA[C/T]TATGCCTGGCCTACT	146691
rs374135516	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17885523	CGAAAAATCCCAAGA[A/T]AAGCACAATCACCAG	146691
rs374168540	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17911273	GATTTAATGGGAGCC[A/G]TATCTGATTACCCGA	146691
rs374192888	in-del	-/GT/GTGT	0.472147	0.114677	intron-variant	TOM1L2	GRCh38.p7	17:17891784	AAAGTGCATGCACAC[-/GT/GTGT]GTGTGTGTGTGTGTG	146691
rs374197679	snp	C/T	6.6569e-05	0.00576889	intron-variant	TOM1L2	GRCh38.p7	17:17882896	AAGTCCTCTGTTTAC[C/T]TGGGCTGCCTGCATA	146691
rs374241020	snp	A/G	0.000148722	0.00862201	intron-variant	TOM1L2	GRCh38.p7	17:17882690	CTTGCCTATGGCCCC[A/G]AAGTATGCAAGTACC	146691
rs374243061	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17970472	AAGGAAAACAATTCT[C/T]GCAAGTTTTCTGGCT	146691
rs374245454	in-del	-/T			intron-variant	TOM1L2	GRCh38.p7	17:17929037	GCTATGGTTCCTAAT[-/T]ACCAAGTCTGAAGAT	146691
rs374266920	in-del	-/G/T			intron-variant	TOM1L2	GRCh38.p7	17:17847943	CGTGAGCTGCAGTGT[-/G/T]GGGGGGAGGCTCCTG	146691
rs374334914	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17959089	AGTTATATCCTTTGT[C/T]ACGAAAATGTAAGTA	146691
rs374340257	snp	A/G	0.0023933	0.0345097	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17844365	TTGCCCCAACTCTCC[A/G]GGCTGGGTCCTCTCC	146691
rs374353689	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17922406	TGGGGCTTTTCAACA[A/G]GAGTGACAAGAATAT	146691
rs374391286	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17912474	ACTTCTCAGACGGGG[C/T]GGCCGGGCAGAGACA	146691
rs374399761	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17923136	GGCGCAGTGGCTCAC[A/G]CCTGTAATCCCAGCA	146691
rs374413505	snp	A/G	1.64732e-05	0.0028699	missense, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17884674	AGAGCGTCCAAGTCT[A/G]CCATGGGAAATTCAA	146691
rs374423271	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17937631	GTGCTCTCAGCTCAT[A/G]AGCAGCTTTCTAAGG	146691
rs374477770	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17935898	ACTCACACTGGTGGT[G/T]CCTGCCTTGTGCAAC	146691
rs374501988	snp	C/T			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17844990	GTTTCCTGACAGAGC[C/T]GCACCCCCTTCCTGG	146691
rs374509790	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17917702	CTCATGCCTGTAAAT[C/T]CCATCACTTTGGGAG	146691
rs374511917	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17857713	GAAGACATGAGCTGT[C/T]ACACAGGTAGGGGCT	146691
rs374588384	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17963834	AACAACAGTAACAGT[A/G]GAGGGAAGGAATCAA	146691
rs374603550	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17868949	ATCCTTTTTCTTACT[A/G]GAGATTTTTTTTCCC	146691
rs374614830	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17852120	ACAAAAATGCCAGCT[C/G]TGTCTATAGCTGGCT	146691
rs374617820	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17909082	GCTACTCAGGAGGCT[A/G]AGGCAGGAGAATGGC	146691
rs374631375	snp	C/G	0.00159617	0.0282053	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17860173	TGGCCACGAGGAGGG[C/G]ATGTCCTCACCAGGC	146691
rs374637608	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17910522	CATGCCCCAGAGGTT[A/C]TACTTTGAATGGTAT	146691
rs374661887	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17907674	CTAGGAGTGCTATTA[C/T]CACAAGAGAACACCC	146691
rs374693901	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17854283	GGGAGGCCGAGGACG[C/T]GCTCCTTGTCAGGCT	146691
rs374738621	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17871152	GAGGCGGATGGATCA[C/T]GAGGTCAGGAGATCG	146691
rs374752531	in-del	-/ATTATT			intron-variant	TOM1L2	GRCh38.p7	17:17903990	TTCACTCAGGAAGAG[-/ATTATT]ATTATTATTATTATT	146691
rs374780153	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17873956	TACTTATTTACTTAC[C/T]TATTTTTTTTTTTTT	146691
rs374785028	snp	A/G	0.00279162	0.0372561	intron-variant	TOM1L2	GRCh38.p7	17:17902761	TCATGGGCAATGGAA[A/G]TCTTTAAAGTGAAAT	146691
rs374805696	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17955104	GGTGTCATAGTTAGT[C/T]TCTCATCTGCTGGTG	146691
rs374836133	in-del	-/CT			intron-variant	TOM1L2	GRCh38.p7	17:17967608	CTAGGCTTTCTCTCT[-/CT]TTTTTTTCTTTTTTG	146691
rs374844096	in-del	-/G	0.000541849	0.0164509	intron-variant	TOM1L2	GRCh38.p7	17:17869324	AAAAAAAAAAAAAAA[-/G]AAATCCGGCTCCCAC	146691
rs374852250	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17938546	AGAGAATGGAGTGAC[A/G]ACGTGCTCTGGAAAA	146691
rs374870930	snp	C/T			upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17972498	CTACGAAGCCCGCCT[C/T]CTATTGGTCGTTACA	146691
rs374872184	snp	A/G	0.00636936	0.0560724	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17858991	GGCGTGAGCCACTGC[A/G]CCCAGCCCTGGGATG	146691
rs374926542	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17943887	TAGCTGCCACAAACA[C/T]ACAGGCCCCTTTTCT	146691
rs374954415	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17948234	CTGTACTGGATAATC[G/T]TGATACCAAGATAAA	146691
rs374981320	snp	A/G			intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17861006	GACAAATGGCCATCA[A/G]AGATGTGGCTCGGGT	146691
rs374996807	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17950439	GCTGGTATTACAGGC[A/G]TGAGTCACTATGCCT	146691
rs375010022	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17898027	ACCTCCCGGGTTCAA[A/G]CAATTCTCCTGCCTC	146691
rs375019071	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17930795	GATAAGACAGTTATT[A/G]CAACTAGACACTAAT	146691
rs375035529	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17954826	GAGGAGAAAACTAAG[A/G]GCAAACACATGCTAA	146691
rs375083600	snp	A/G	4.12686e-05	0.00454231	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17866334	AGGGAAGATGGGGGC[A/G]CTGTGTTCCCCACCA	146691
rs375123712	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17946199	CAATTTTGTATAAGA[A/G]CTTTATTGAGATATA	146691
rs375139801	snp	A/G	6.61397e-05	0.00575026	synonymous-codon, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17869375	GTTGTTGAGGTCATC[A/G]TTCACATGCAGCAGC	146691
rs375171709	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17902968	GGCTCGCACAATAAG[C/T]GAGTGGTGACCTAGA	146691
rs375201706	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17850738	CTATGGGCTGATGTC[A/G]GGGAGGAGGGGCAGC	146691
rs375245609	in-del	-/CATATGTGAAAAAG	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17941454	AGCAGGAAAACAAAA[-/CATATGTGAAAAAG]CTAGACAAAAAGCTG	146691
rs375256018	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17929196	AGCGTCAGGCGGGGA[A/G]GTCAAGAACTGCCCA	146691
rs375284977	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17927751	TCACTGCAGCCTCAA[C/T]CTTCCAGGCTCAAGT	146691
rs375303274	snp	A/C/G	0.000148722	0.00862216	synonymous-codon, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847734	GGGCGAGGGGAGGTC[A/C/G]GGAACCATTTCAGCA	146691
rs375354925	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17961669	ATGAGGTGAGGAGAT[C/T]GAGACCATCCTGGCT	146691
rs375361037	snp	A/G	0.000248445	0.0111427	intron-variant, missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17893716	GGGTTGTTCTTGGGA[A/G]ATATAATTTTGACCA	146691
rs375411914	snp	G/T	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17853239	CAGCATCTCCAGAGA[G/T]AAAATAGTCCCACAC	146691
rs375415649	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17874195	TCCTGACCTCATGAT[A/C]TGCCCGCCTTAGCCT	146691
rs375417049	in-del	-/AGAGATCTCCTCTTGTCCC			intron-variant	TOM1L2	GRCh38.p7	17:17867217	CACACACCTGGGCCC[-/AGAGATCTCCTCTTGTCCC]TGGAGGGAGGGTGGC	146691
rs375428917	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17914888	TTTAGGTAAAAAAAA[A/T]TTTAAAAAGAGCAGT	146691
rs375497463	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17923250	CTAAACATACAAAAA[A/G]ATTAGCCAGGCGTGG	146691
rs375520114	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17888119	AGCTGCCTTTTCAGA[A/C]AGCAAAGTGATGCAG	146691
rs375527754	snp	C/T	0.00318978	0.0398085	intron-variant	TOM1L2	GRCh38.p7	17:17938019	ACTGGGATTTTGCCA[C/T]ACGGTGGCTCTGCTT	146691
rs375549455	snp	A/C/T	0.000148275	0.00860913	missense, upstream-variant-2KB, intron-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17862791	ATGTCAAAGCCGTCA[A/C/T]GGGGATTACATTGCT	146691
rs375618380	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17965584	TGAGGGCAGCACAGC[A/G]TGACAGGATACCAGC	146691
rs375619853	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17947118	CCACACAGTAAATAC[A/C]ATCTTCAGCAAGGAA	146691
rs375630726	in-del	-/A			intron-variant	TOM1L2	GRCh38.p7	17:17959682	GGAGCAGCAAAAAAA[-/A]CTCCACAGTGTCCTA	146691
rs375646820	snp	C/T			intron-variant, upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17971878	GAGGTGGCACCAGTG[C/T]CCGGGAGGAGGCCCG	146691
rs375650300	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17848358	CAAGATGAGCTTGGG[C/G]AGGCAGGATGTGAAG	146691
rs375692980	snp	A/G	4.95291e-05	0.00497615	intron-variant	TOM1L2	GRCh38.p7	17:17848804	AAAGGGGGCTGTAAG[A/G]CCACTGGCCAGGCCA	146691
rs375792381	snp	C/T	3.6507e-05	0.00427226	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847609	AGCGGGGACCCGCCA[C/T]CTGGGGAGGCAAACC	146691
rs375792854	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17872052	TGGGGCCTGCCAGAC[A/G]TGGTCTGGATTGCCA	146691
rs375807707	snp	A/G	0.000329587	0.012833	intron-variant	TOM1L2	GRCh38.p7	17:17898547	GGGGCAAGGCCAGGA[A/G]CAAGGAGTTCCCCAG	146691
rs375827085	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17918507	GAAGAGAAGACCCAT[G/T]TGAGTCCTTATTCCA	146691
rs375848127	snp	C/T	1.68007e-05	0.00289828	intron-variant, missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17893810	CACATGTCTCCAGCA[C/T]CTGATGTGGGGAGGG	146691
rs375892178	snp	C/G/T	4.95572e-05	0.0049776	intron-variant	TOM1L2	GRCh38.p7	17:17847814	AGGCAAGGGTCAGGG[C/G/T]TGGTGAGGGCAGGCC	146691
rs375917269	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17910581	ATTATTATTATTATT[A/T]TTATGTGAGACAGAG	146691
rs375941842	snp	A/T	0.00318978	0.0398085	intron-variant	TOM1L2	GRCh38.p7	17:17923564	GCGCAGTGGTGAGCA[A/T]CTGTAGTTTCACCTA	146691
rs375967044	in-del	-/CT			intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17858526	GATTCAAGCAATTCT[-/CT]GTCTCAGCCTCCCAA	146691
rs376062118	snp	C/G	0.00478085	0.0486577	intron-variant	TOM1L2	GRCh38.p7	17:17869002	GGATCATCAAAGGAG[C/G]AGGTGCAGAAGCTCT	146691
rs376068277	snp	A/G	0.000256777	0.011328	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847605	TGCGAGCGGGGACCC[A/G]CCATCTGGGGAGGCA	146691
rs376102381	snp	A/G	0.00199481	0.0315187	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	TOM1L2, DRC3	GRCh38.p7	17:17972946	CGCGTCTGCTGCGTG[A/G]AACCGCCGAGTTCCC	146691
rs376201287	snp	G/T			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17844259	GGGGGCCCAGGGTGG[G/T]GTGTGGCAGCGGGAA	146691
rs376234563	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17871050	CCCCAAGTACTTCTG[A/G]GAGAATTAATTAATG	146691
rs376236442	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17921470	TAATGGAATAACTTA[A/C]GTGTGAGTCAGTGTG	146691
rs376245975	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17945244	TAGGTGGAAAGAGCC[A/G]AATGTTTCACCACAC	146691
rs376386507	snp	C/T			missense, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17884715	CTTCAGCTCCTCATA[C/T]ATGTGCACAACGCCG	146691
rs376481224	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17917688	GCTTCCCAGGCCAGC[C/T]CATGCCTGTAAATCC	146691
rs376511664	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	TOM1L2, DRC3	GRCh38.p7	17:17972838	ACACGGAGATGTGGT[A/C]ACGTGACTTGTCAAC	146691
rs376559843	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17917200	AGCTGGGCGTGGTGG[C/T]GCACACCTGTTGTCC	146691
rs376561708	snp	C/T	1.73981e-05	0.00294936	intron-variant	TOM1L2	GRCh38.p7	17:17907569	GGTTTACATTTCTCC[C/T]GGAATAAGTGGGCCT	146691
rs376565471	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17865438	CTGGAGTGCAATGGC[A/G]CGATCTCGGCTCACT	146691
rs376566158	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17962639	ATATTTAATGCCATT[C/G]AACTGCACACTTAAA	146691
rs376577391	in-del	-/G			intron-variant	TOM1L2	GRCh38.p7	17:17955351	TTTTTTTTTTTTTTT[-/G]TTTTTGAGACAAGAG	146691
rs376591263	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17904043	TCACTACATTTCCTA[A/G]GCTGGTCTCAAACAC	146691
rs376709967	in-del	-/ACATACATACAT			intron-variant	TOM1L2	GRCh38.p7	17:17894935	AACTCTGTCTCAAAA[-/ACATACATACAT]ACATACATACATACA	146691
rs376806732	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17947284	CTGCCTCAGCCTCCC[A/C]AAGTGCTGGGATTAT	146691
rs376856791	snp	C/T	0.000332244	0.0128846	intron-variant, upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17972238	CCGCCGTTGCCCAGC[C/T]TCCTGCCCCACACGC	146691
rs376873550	snp	A/G	0.000461893	0.0151899	intron-variant	TOM1L2	GRCh38.p7	17:17850968	CTATGGAGGCGGCAA[A/G]CAGCGGGCCAGGCAG	146691
rs376937237	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17964152	TGGAGGGAGCAATAA[C/G]ATATGTAACCAAGTC	146691
rs376964995	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17956949	CTGAAGGGCTCCTCA[A/G]GCACAGCCAGAGAAG	146691
rs376983851	snp	A/G	0.0023933	0.0345097	intron-variant	TOM1L2	GRCh38.p7	17:17891870	GGGCAGAACAGGGAC[A/G]AGGGACAACCCTAGG	146691
rs377004879	in-del	-/ACAG			intron-variant	TOM1L2	GRCh38.p7	17:17965048	GGGCTTCATAGACAG[-/ACAG]TGTCCCTACCCTTGA	146691
rs377010407	snp	C/T	3.31093e-05	0.00406861	intron-variant	TOM1L2	GRCh38.p7	17:17879577	TCCTCCAACAGTGTA[C/T]GGTGGAAGAGCTGCC	146691
rs377078543	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17967854	CTCAGGTGATCCACC[C/T]GCCACGGCCTCCCAA	146691
rs377101456	snp	A/G	1.64792e-05	0.00287042	synonymous-codon, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17882768	CTGCGGTGCGGAGTA[A/G]GGAGCAGGAGGCGGC	146691
rs377113195	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17896849	ACAGATATGAAGTCC[A/G]GAGAGGGCCACAGGA	146691
rs377125715	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17910150	GCTGGGTCAGGGAGT[A/C]GCAGGGTGGGGATCA	146691
rs377150768	snp	A/G	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17864789	AGTCTTGGGATTACC[A/G]GTGTTACACTTTGAA	146691
rs377155114	snp	A/G			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847523	GTGGCATTTCCATGG[A/G]AACACAGGTGTGCAG	146691
rs377161114	in-del	-/GAG			intron-variant	TOM1L2	GRCh38.p7	17:17926655	ATTGCTTGAGCTCAG[-/GAG]TTCAAGACCAGCCAA	146691
rs377205086	snp	C/T	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17940979	GTAAGATTTGTACCA[C/T]TGGGATTCTCAATCT	146691
rs377211668	snp	A/G			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17845602	GCCCGAGGTCGGACC[A/G]CCCACCACCCGCAGG	146691
rs377278051	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17945010	CGCCGCCACACTAAT[C/T]CTTCATCCTCCGGGG	146691
rs377292312	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17889623	GAGGTGTTAGGGAGG[C/T]ACGTCTGTGTGGCCC	146691
rs377296337	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17912609	CGGGCAGAGACGCTC[C/T]TCACTTCCTAGATGG	146691
rs377302222	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17958817	ACCAAGGTACATTTC[A/G]GTGTTGGAACTTTTA	146691
rs377333411	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17914721	CCAGTCCTCTGGCTG[G/T]GTATTGCATTCATGT	146691
rs377346123	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17931036	AAAATATAAAATGTT[C/T]TTCCTGTAACTTAGC	146691
rs377359555	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17953589	CCCCTAACCCAGGAG[A/G]AAACCTGTGCCCCAC	146691
rs377410329	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17957822	TTAAGAAAAACTAGG[C/T]CAGGCGTGGTGGCTC	146691
rs377411236	snp	C/T	0.0425829	0.139564	intron-variant	TOM1L2	GRCh38.p7	17:17939413	GACAACTAAAAATTT[C/T]GAACACTAGTTGGAT	146691
rs377411467	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17877921	CTCCCCCCAAAACAC[A/G]AAGTATTCCTGCTGT	146691
rs377441634	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17903507	AGTCCCAGCTACTCA[G/T]GAGGCTGAGGCAGGA	146691
rs377509115	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17934093	AAATCAAGACACAAA[C/T]TAGTATATTTTTTAT	146691
rs377510045	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17953895	TGCCTTGCCTCTTCT[C/T]CCAAGTCACACAAGG	146691
rs377512079	snp	A/G			upstream-variant-2KB, intron-variant	TOM1L2, DRC3	GRCh38.p7	17:17973358	AATGATTTCATCTTG[A/G]TACTGTATATACCGC	146691
rs377530471	snp	A/G	3.29636e-05	0.00405964	intron-variant	TOM1L2	GRCh38.p7	17:17866960	AGAAGTAAGGAGAGA[A/G]GATGCCTGTGATATG	146691
rs377548130	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17851611	GAAACACAGCAAAAA[C/T]GAGGGCTCTGATGAC	146691
rs377565785	in-del	-/ACA			intron-variant	TOM1L2	GRCh38.p7	17:17956064	ATGGAGTAAGCAGCA[-/ACA]TTTGTTTCAAAGAGC	146691
rs386352375	snp	G/T			missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17898668	TTTTTCCAGGCCAAA[G/T]GATGCCATTCGAGCC	146691
rs386795953	multinucleotide-polymorphism	AT/GA			intron-variant	TOM1L2	GRCh38.p7	17:17918725	TGGGCTCCAGCACCT[AT/GA]TAGTACAGTTCACAC	146691
rs386795954	in-del	C/TT			intron-variant	TOM1L2	GRCh38.p7	17:17926261	TCTGAACATACAGAC[C/TT]AAGGATAAAAGCCTG	146691
rs397704474	in-del	-/A			intron-variant	TOM1L2	GRCh38.p7	17:17879414	TAATCAGGAAAAAAA[-/A]TGTTATTAAGGAAAA	146691
rs397704964	in-del	-/A	0	0	intron-variant	TOM1L2	GRCh38.p7	17:17875284	GAAAAAAAAAAAAAA[-/A]GGACAGAAGGTGAGA	146691
rs397732252	in-del	-/A	0	0	intron-variant	TOM1L2	GRCh38.p7	17:17869323	AAAAAAAAAAAAAAA[-/A]GAAATCCGGCTCCCA	146691
rs397763413	in-del	-/T			intron-variant	TOM1L2	GRCh38.p7	17:17938780	GTTTTTTTTTTTTTT[-/T]TAATATTTTGTAAAG	146691
rs397810383	in-del	-/CA			intron-variant	TOM1L2	GRCh38.p7	17:17946280	TAGTACATATATTCA[-/CA]GAGTTGTGCAACCAT	146691
rs397856352	in-del	-/T			intron-variant	TOM1L2	GRCh38.p7	17:17915858	TTTTTTTTTTTTTTT[-/T]GGTTGTTAAGCTGTA	146691
rs397856845	in-del	-/T			intron-variant	TOM1L2	GRCh38.p7	17:17962337	ATATTTTTTTTTTTT[-/T]AGGGATGGAGTCTCG	146691
rs397857287	in-del	-/CT			intron-variant	TOM1L2	GRCh38.p7	17:17852120	ACAAAAATGCCAGCT[-/CT]GTCTATAGCTGGCTT	146691
rs397967462	in-del	-/T			intron-variant	TOM1L2	GRCh38.p7	17:17954329	TTTTTTTTTTTTTTT[-/T]GTGATGGAGCTTCGC	146691
rs397968087	in-del	-/C			intron-variant	TOM1L2	GRCh38.p7	17:17904813	GATGCCACCCTTGGC[-/C]TACGGGACACATTTC	146691
rs398030468	in-del	-/A	0	0	intron-variant	TOM1L2	GRCh38.p7	17:17863583	AGACTCTGTCTCTTT[-/A]AAAAAAAAAAAAAAA	146691
rs398030469	in-del	-/T	0	0	intron-variant	TOM1L2	GRCh38.p7	17:17885949	TTCCAAAGAACAGAA[-/T]TTTTTTTTTTTTTTT	146691
rs527260871	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17894963	CATACATACATACAT[A/G]CATACATACATACAT	146691
rs527282562	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17862207	GAAAGCTCAAAACAT[G/T]TACAGTGCCTCCCTG	146691
rs527291985	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17958692	CAGTAAGAAATATAT[A/G]TTTGGTCTTTGTCCA	146691
rs527311662	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17964431	TTGTTCTACAATGTC[A/G]CCTCTTCAAGGCATG	146691
rs527316065	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17862928	GCCCCCAAGCTAGGA[C/T]GCCAGCCAGGTGGGT	146691
rs527317166	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17927319	TTACCATGTGAGTAA[C/T]GGGCAGAGAGAACCT	146691
rs527345181	in-del	-/T			intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17860219	CCTGGCTGGGCTCTC[-/T]TAATGCCCACGCTGG	146691
rs527352677	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17951596	AACTGAAGAATGGTG[A/G]CCAAAGGGTTTTTAG	146691
rs527353484	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17856118	ACCACCACCAGCTGC[C/G]AAGGCCACCCTCAGG	146691
rs527385920	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17849840	AGAGAAGCAATTTCT[C/T]TTCGAGACAGCCCCT	146691
rs527406610	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17899651	GCACAAAGCCCCTGT[A/G]CTGACCTGACCCATC	146691
rs527414515	snp	A/C/T	0.0142982	0.0835538	intron-variant	TOM1L2	GRCh38.p7	17:17927935	GTCAGCTATACTTTT[A/C/T]AAAAGATTCCTTATC	146691
rs527494790	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17876310	AGAAGTGACGCAGCA[A/G]GGTTTTCAGCTGATG	146691
rs527496209	in-del	-/AGAC	0.0058626	0.0538231	intron-variant	TOM1L2	GRCh38.p7	17:17965042	CTGAGGGGGCTTCAT[-/AGAC]AGACAGTGTCCCTAC	146691
rs527562222	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17922302	TCCCAGGGCCAGGGC[A/C]TCGGTGAAGGGGAGC	146691
rs527608383	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17922909	TTAACTGCCTCCTGG[A/G]GTGTGAGCAGAGAGG	146691
rs527614673	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17966011	CTGTAATCCCAGCTA[C/T]TTGGGAGGCTGAGAC	146691
rs527654569	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17885715	GGATCACGAGGTCAG[A/G]AGATCAAGACCATCC	146691
rs527708486	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17870831	CACACAGTGAAAAAG[C/T]CCAGTAATCATCTGC	146691
rs527726252	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17931203	CTTTTCGTTACTACC[C/T]ATTTTTACCCATCCT	146691
rs527736386	snp	C/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17871276	CTTGGGAGACTGAGG[C/G]AGGAGAATGGCGTGA	146691
rs527780448	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17871328	GTGAGCCGAGATCAC[A/G]CCACTGCACTCCAGA	146691
rs527788402	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17923792	AAGCCCAGGAACTGG[A/G]GGCTGGGAGACACTC	146691
rs527793286	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17916296	GCCAGGATGGTCTCG[A/G]TCTCCTGACCTCGTG	146691
rs527823399	snp	A/C	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17968898	ATGAACAGCCCTCAG[A/C]CTCAAAGAAGCCAGT	146691
rs527866869	snp	C/G	0.00597247	0.0543191	intron-variant	TOM1L2	GRCh38.p7	17:17952317	ATTACCTCTGGGGAG[C/G]CTAGTTGGGCTGAGA	146691
rs527880954	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17892742	ATTTCCCCTACTCTT[A/G]AGGCTAGGCCTGGTG	146691
rs527916516	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17945634	TATACATCTTAGTTA[A/T]TCATTGATATTTTGT	146691
rs527926503	snp	C/T	0.00159617	0.0282053	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17844171	AGGGGCTGGCCTGGC[C/T]CCAGGTGGGCCCATG	146691
rs527987822	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17930515	ACATCTTGTCCAAGA[C/G]ATAAAATACCCTTCC	146691
rs527994888	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17939385	CAGTCTTAAAAAATA[C/T]ATGACATTATGAGAC	146691
rs528014348	snp	G/T	0.00716266	0.059414	intron-variant	TOM1L2	GRCh38.p7	17:17852789	AGAATCACTTGAACC[G/T]GGGAGGCAGAGGTTG	146691
rs528027873	snp	A/G	8.23649e-05	0.00641683	synonymous-codon, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17884739	AACGCCGGTGAGATC[A/G]GGACTGCTTCGAAAG	146691
rs528078685	snp	C/T	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17939239	ATACCAGGCAAAAAG[C/T]TGGCAGCTGGCTTTT	146691
rs528090364	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17895235	CTTCCCATGCCAACA[A/G]CCCCCAGTGCCACAG	146691
rs528140882	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17931999	TATCACTGACCAATG[C/T]CTTGATAAACTACAG	146691
rs528167717	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17916761	GGCGCAGTGGCTCAC[A/G]CCTGTAATCCCGATA	146691
rs528168905	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17846469	GAATACATGTTACCA[G/T]CCCCTAGCTGCTCTG	146691
rs528238530	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17887572	ACCTCTGCCTCCGGG[A/C]TCAAGCAATCCTCCC	146691
rs528243007	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17879513	CATGGACTATCAACA[A/G]CAGGGCCACTGGACC	146691
rs528264383	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17864499	ACAGGCGTTAGCCAC[C/T]GCACCCGGCTTTTTT	146691
rs528294689	snp	C/G	0.00318978	0.0398085	intron-variant	TOM1L2	GRCh38.p7	17:17960973	GTGCATTAAAGGACA[C/G]TATAAACAGAGTATA	146691
rs528307026	snp	C/T	0.00676609	0.0577691	intron-variant	TOM1L2	GRCh38.p7	17:17961607	GGCCGGGCACGGTGG[C/T]TTACACCTGTAATCC	146691
rs528316549	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17864856	CTGACTGAAGGCAGA[C/G]ACATCTGTTCTGATA	146691
rs528353916	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17872942	CAAGTCAGGGGAGTG[C/T]GGCAGTAGGTTGTGG	146691
rs528362052	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17851018	GGGAGACAGAACACC[A/G]GAACAAAGGAAATCA	146691
rs528362234	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17858270	TGTATTCTTTTTCTA[A/G]ACTCTTGAATACTAA	146691
rs528376139	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17901267	CAGATTAGATAGTGT[A/G]GAGTTGGAAACCAGG	146691
rs528398829	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17851413	CAGAGCGGGGTACAG[G/T]TGCTCAGAGGGCAGG	146691
rs528403106	snp	C/T	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17901921	GGGTGCTCTGGCTCA[C/T]GCCTGTAATCCCAGC	146691
rs528417929	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17954152	TGGTCTAAACCATGA[A/G]CAAGAGAGAAGGGAT	146691
rs528424388	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17970307	CTGACCTTGTGATCC[A/G]CCCGCCTCAACCTCC	146691
rs528444059	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17963216	TCATACAAAAGCAGT[C/T]GCATCGAGAAGCAAA	146691
rs528450498	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17910953	TTGCTGAATGCAAAA[C/T]GCTAAAACCAGTCCT	146691
rs528482954	snp	C/T	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17866525	GAAGAAAAGTATCAG[C/T]GCTGCTCTAGTACAG	146691
rs528504740	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17955967	TTCATTCCTCCCAAT[A/G]GGTTCGTGGTCTGCG	146691
rs528517665	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17947936	TCTTTCCAGAATATA[C/T]CTGGTTACAGTCCAA	146691
rs528520721	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17859738	ACACAAAAATTAGCC[A/G]GCTGTGGTGGTGGGC	146691
rs528528692	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17904983	TCACCTTGGCATCCC[A/G]TAGCTGCTATACCTC	146691
rs528536433	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17853112	GCCTTGAGACATTCC[C/T]GGAACAGGACACACC	146691
rs528538687	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17956529	GCGGTCGATGGGACC[A/G]GGCGCAGTGGAGCAG	146691
rs528543998	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17860198	CCAGGCAGTATCCTG[A/G]TAGGCCCCTGGCTGG	146691
rs528552477	snp	A/T	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17949034	GTGACTGTCCCATAG[A/T]CCAGAGAATGGGGAG	146691
rs528568597	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17853614	CCTAGATTTTTCCAA[A/G]TAAGTAGTATGTTTA	146691
rs528584938	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847062	GGTCAAGAAGGTGAG[A/C]GACCCCCACCATGGA	146691
rs528589559	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17946056	TTTTTCATATTTTTT[G/T]GTAAGACGGGGTTTC	146691
rs528623318	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17904377	TATTTGAGCAATTCA[C/T]TGGAAAATAAGAGTT	146691
rs528652557	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17865470	CAACCTCTGCTTCCC[A/G]GGTTCAAGCAATTCT	146691
rs528653796	snp	G/T			missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17907486	TCACAGATCTCCATA[G/T]TCAACGTCCAATCCT	146691
rs528681848	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17970797	AATTTCATAAGCAAA[G/T]CAGAAAATAAACAAA	146691
rs528683798	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17880231	TAAACACTAGGATCC[C/T]TCTGAGAGGCTGGGC	146691
rs528702287	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17873219	ATTTTCAAACATACA[A/G]CAAAACAGGAAGAAT	146691
rs528718799	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17926228	CTGGCCTAAACATAA[A/G]TAAGCTTCATTACTT	146691
rs528741251	snp	A/G	0.00279162	0.0372561	intron-variant	TOM1L2	GRCh38.p7	17:17865860	AGTGATTCTCCTGCC[A/G]CAGCCTCCCGAGTAG	146691
rs528748348	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17971739	GAAGCAGACCAGCAG[C/T]TGGCACCACCTCTAG	146691
rs528761609	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17918052	ACGTTTTATAGTTTT[C/T]GGTGCACAATTTTTT	146691
rs528799689	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17918810	ACCGGCTTAATGAGC[C/T]GTTAAGTATCTTCTT	146691
rs528812603	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17910324	TGAGCTCTGTGAGGG[A/C]AGGGACTAGGTCTGT	146691
rs528845925	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17874479	TTTCACCATGTTGGC[C/T]AGGCTGGTCTCAAAC	146691
rs528869359	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	TOM1L2, DRC3	GRCh38.p7	17:17972859	ACTTGTCAACTTTCA[A/C]CCAGGATGTCTCCCT	146691
rs528882080	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	TOM1L2, DRC3	GRCh38.p7	17:17973519	TCCCTTTTTATGGCC[C/T]CCGGAGCTTACATGT	146691
rs528882376	snp	A/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17875289	AAAAAAAAAAAGGAC[A/T]GAAGGTGAGAAGGTG	146691
rs528923247	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17919852	CCTCATTTAACCCTA[C/G]CATCCCACGCCCCAG	146691
rs528933118	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17906320	TTTTTGTAAAGACAA[G/T]ATTCAACCGTGTTGC	146691
rs528936565	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17960691	AAAATATGACTGACA[A/G]GCCTGGGTGACACAG	146691
rs528937046	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17928208	TCATAACTTTGACCC[A/G]GCAATAGCCCCCTAA	146691
rs528944621	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17868270	GAGGTTTATTCACCT[A/G]TCAGGTGGGCACAGA	146691
rs528947567	snp	A/T	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	TOM1L2, DRC3	GRCh38.p7	17:17974381	TTCCCTTATTTTTTT[A/T]ATTTTTTGAGATGGA	146691
rs528960107	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17965139	GCTTTCATGGTAGAG[A/G]GAATGATCTTCTGGT	146691
rs528979404	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17939213	GTGCCTAACTTTTGG[C/T]GTTGAGACGAATACC	146691
rs528992859	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17921816	GTGCAGTCTGCTTTG[C/T]TGCCAATTTCTTCTT	146691
rs529021335	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17941871	GGCATGCACCTATAG[A/T]CCCTGCTACTAGGGA	146691
rs529049720	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17897081	GGAAGGCAAGTAAAC[A/G]CAGAGTTCACTTTAG	146691
rs529050799	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17889195	ACGGATGGCTGGAGG[A/G]CAGCCAGAAGACAGA	146691
rs529060391	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17926763	CTTGAGAGGTTGAGG[A/C]ACAAGAATCGCTTGA	146691
rs529072565	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17949490	CCACTCCGATGCTAC[A/G]ATCTGACCTGTGCCA	146691
rs529096384	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847575	AGGAGTGGCCAGTGC[C/T]CGGTGTCCACGGGGT	146691
rs529111911	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17942769	CAGTCACATCAGCAC[A/G]GTAGTTAGTATAGAA	146691
rs529139157	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17943420	GACAGAGGGCTGAAT[C/G]CTGCTGCCTGGAGAG	146691
rs529167857	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17935241	GGGGAGGCAGCTGAA[C/T]TGTGAGTCAGGTCTA	146691
rs529197885	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17881871	ATCCCTACACACACA[C/T]TGCTTGACCCCTCTG	146691
rs529202897	snp	A/T	0.00279162	0.0372561	intron-variant	TOM1L2	GRCh38.p7	17:17935993	CAGCAGCTAGTGGCT[A/T]TTCTGGAATGCAAAT	146691
rs529205025	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17927451	AGGACCTGCATGCAG[A/T]CCTTTCTTGATAAAG	146691
rs529221238	snp	G/T	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17890365	AAATTGCTAATATTT[G/T]GCCATTTTTGACCAA	146691
rs529253479	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17891642	GGTCAGAAAGCTCTA[C/T]CACAGGACATGCTTT	146691
rs529295929	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17883518	GGCGGGTGGATCACA[A/G]GGTCAGGAGATAGAG	146691
rs529332153	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17929155	GGGTACAAGCCAGAA[C/T]GCAGTCGGGACTGTG	146691
rs529333535	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17937709	TTTTCCTGCAGGCTG[C/T]AGGAATGAGAAAGTG	146691
rs529333598	snp	C/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17948478	ATGGTGAAACCCCGT[C/G]TCTACTAAAAATACA	146691
rs529352382	snp	C/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17849526	CAAGGAGCCATGGAG[C/G]CTCTGTGCACTCAAA	146691
rs529365872	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17950318	TGCACCACTATACCC[A/G]GCTCCTTTTTTTGAA	146691
rs529369803	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17929759	TGATAAGACCTTTCC[A/C]GAGAATTACACACAC	146691
rs529400488	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17904946	TCCTGCCAGGTGAGC[A/G]TTCAAGGGCAGGCTG	146691
rs529462914	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17869067	GGGGCTGGGGGTGGC[A/G]GGGCAGTGGGGAAAG	146691
rs529485298	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17861289	GTGGCCTCATCTCAC[A/G]GGGTGAGGTGAAGAC	146691
rs529487067	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17956894	AGGCGGCTCCGGCCT[C/T]GGCCAGCCCAGGGAG	146691
rs529488726	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17965774	GCAAGATGTATAAAG[C/T]GCCCACTTCAGTCTC	146691
rs529496573	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17861972	GTGGTCTCTGGGACC[C/G]GGGCCTGTCACTGAT	146691
rs529517114	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17969677	ATTTTCCTTCACAGG[G/T]CACAGACGGGCCAGT	146691
rs529536863	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17898218	TGTGAGTCACCGCGC[C/G]TGGCCAACATTTTTA	146691
rs529542526	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17950867	TGGAAACTGCAAGAT[C/T]TGGGAAAACCTAGGC	146691
rs529571297	snp	C/T	0.000184265	0.00959681	intron-variant	TOM1L2	GRCh38.p7	17:17898726	TCCCACTTGAGGACA[C/T]GATCCTACAGATATG	146691
rs529573591	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17951402	TAGAGATGAAAAGGA[C/G]GAACATTTAGTACTT	146691
rs529602661	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17944260	GTGGACAGGTGAGGA[C/T]GGCAGGATGCTGAGC	146691
rs529620616	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17848940	TGTCTGCCCATGGCC[A/G]CCCTAGGACAGCACT	146691
rs529651113	in-del	-/TTG	0.0023933	0.0345097	intron-variant	TOM1L2	GRCh38.p7	17:17938770	GGTTGAAAGGGTTTT[-/TTG]TTTTTTTTTTTAATA	146691
rs529656701	snp	C/T	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17863750	GACAAGGTCTCGTTA[C/T]GTTGCCCAGGCTGGT	146691
rs529668286	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17907645	AGCAGATGGGCTGAG[C/T]CAACAGAGCCATTCT	146691
rs529681556	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17952443	GTTCCCAGGCTGGAG[A/T]GCAGTGGTGTGATCT	146691
rs529681660	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17960905	GATAAGGGCATGACA[C/T]GGAAGGTACAAGCAA	146691
rs529693782	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17953248	TCTTGTCACTGCACT[C/G]CAGCCTGGGCAACAG	146691
rs529748053	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17844733	GCGCCATTCTCTGCC[A/G]CCCAGTGGCCAAAAA	146691
rs529768024	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17945724	CACATAAAACTGGAT[A/C]TTAAGTATCTTAATG	146691
rs529807170	snp	C/T	0.00716266	0.059414	intron-variant	TOM1L2	GRCh38.p7	17:17900144	CTTGAACCTGGGAGA[C/T]GGAGGTTGCAGTGAG	146691
rs529822557	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17908472	TCAAAATAAAAACTT[C/T]CAGGCATCAAAGGAC	146691
rs529827293	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17892846	ATCTTGATGTCCACA[C/T]GGTGATAAACTCAGG	146691
rs529835854	in-del	-/T	0.00835141	0.0640778	intron-variant	TOM1L2	GRCh38.p7	17:17847936	TCGTGAGCTGCAGTG[-/T]TGGGGGGAGGCTCCT	146691
rs529845302	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17901058	TGTGGGGGCCACGGG[A/G]TGGGAAATCAGACAG	146691
rs529874157	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17954427	AAATGATTCTCCTGT[C/T]TCAGCCTCTCTGGTA	146691
rs529898268	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17877112	AAATACAGCCACATA[C/T]CCATGAGTCTGCAGG	146691
rs529904017	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17966730	CAGAGCCTCGATTTC[C/T]TTATGTGATACAGGG	146691
rs529909700	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17884945	TGCCACGACACAGCT[A/G]GTGAAACCCTGGCTT	146691
rs529911007	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17967929	TCTCTCCCTAAACCA[C/T]GCTTTCTACTCAGGA	146691
rs529934890	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17869830	GGTACAGACTGCCTC[A/G]TTCCTTTCTGTGTGT	146691
rs529977941	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17870588	ACATGAAGGATAAGT[C/G]TCTCCTTCTCACAGC	146691
rs529998722	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17914670	ACTGACTTTGGTTAA[A/G]ATTGCTCCAAATCTC	146691
rs530002000	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17910799	GTCTCGAACTCCTGA[C/T]CTCAGGTGCTCCACC	146691
rs530020478	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17879301	TACATCAAAGCACCT[A/G]CAGTGGTTATTTACA	146691
rs530055227	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17872051	TTGGGGCCTGCCAGA[C/T]GTGGTCTGGATTGCC	146691
rs530076679	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17925424	GGCAAACTTTAAAAA[A/T]TTTTTATGTTATTAC	146691
rs530096090	snp	A/C	0.00318978	0.0398085	intron-variant	TOM1L2	GRCh38.p7	17:17864981	AAGTAGACGAGAAAT[A/C]TTTTTTAAAAAGGAA	146691
rs530096464	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17877351	TGTTGGTGGGAACAT[C/G]TGGGTTGTTTCCATG	146691
rs530159653	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17880305	GGGGAAGACGACAGG[A/G]GAGACACCTTCCCCA	146691
rs530170514	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17909112	CGTAAACCCAGGAGG[C/T]GGAGCTTGCAGTGAG	146691
rs530184569	in-del	-/A	0.486133	0.082104	intron-variant	TOM1L2	GRCh38.p7	17:17961871	GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA	146691
rs530238240	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17885823	CCAGCTACTCAGGAG[A/G]CTGAGGCAGGAGAAT	146691
rs530246879	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17917880	GGATGACTTGAGCCC[A/G]GGAGGTCAAGGCTGC	146691
rs530329016	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17915272	CCAAACTCAGGCTTT[A/G]CTAGCAGGTGAGACT	146691
rs530404394	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17938168	TGAGAGGGAGGCAGT[C/T]AGATCCAATTAAGCA	146691
rs530408511	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17940120	ATCACTTGAACCCAG[A/G]AGGCGGAGGTCGCAG	146691
rs530430985	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17880280	CTGCTGCGGCAAGAA[C/T]GAGAGAACAGGGGAA	146691
rs530439465	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17931742	GATCCAGGTTCAGAA[C/T]GCAAAGCTCCTATAA	146691
rs530441337	snp	A/T	0.00438332	0.0466095	intron-variant	TOM1L2	GRCh38.p7	17:17924365	AATACAATGTTTTTT[A/T]AAAAAAACTCTGTGA	146691
rs530471721	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17933281	CCAAAGGACTTTGCC[A/G]TCTTATTTATGAAGA	146691
rs530544377	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17926665	CTCAGGAGTTCAAGA[C/T]CAGCCAACATGGTGA	146691
rs530566730	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17846960	CTCTCCCTGCCCAGG[G/T]AGCCTGCAGGGACCC	146691
rs530588771	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17902108	TTGAGCCTGGGAGGC[A/G]GTGGTTGTGGTGAGC	146691
rs530610239	snp	C/T			intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17860712	GCCCCTGCAAACAGA[C/T]GTGCATTCATACACA	146691
rs530614466	snp	A/C	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17865737	AAACATGGCAGGTGA[A/C]CTTTCTTTTTTTTTT	146691
rs530617648	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17858338	AGATGAGGTCTCACT[A/G]TGTTGCCCGGACTGG	146691
rs530626438	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17903017	GTCCACCTTCCTCCC[A/C]TTCATCCACCTGCCT	146691
rs530701796	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17910156	TCAGGGAGTAGCAGG[G/T]TGGGGATCAGAGATC	146691
rs530703078	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17954398	GCTCACTGCAACCTC[A/T]GCCTCCCAGATTCAA	146691
rs530710477	snp	A/G	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17962292	TGCAAGACTAGAAGA[A/G]TTGTAGAGATGGCCA	146691
rs530752123	snp	A/G	0.00557542	0.0525036	intron-variant	TOM1L2	GRCh38.p7	17:17910253	AGCTCAGGATCGTCA[A/G]TGGCAGAGCCAGGAC	146691
rs530757856	snp	C/T	0.0023933	0.0345097	intron-variant	TOM1L2	GRCh38.p7	17:17895407	CAAGTGGGCTTTACC[C/T]GGACAAAACATAGCC	146691
rs530761595	snp	G/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17851464	ATGCAGGGGGTCTGT[G/T]TGCTCCGCTGAAGAG	146691
rs530770981	snp	A/C	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17858835	ATCCACCCACCTCAG[A/C]CTCTCAAAGTGCTGG	146691
rs530774650	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17940328	AATCAATAATTGGTA[A/G]CTTTATACAACCCTA	146691
rs530783474	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17933384	AGGGAAACTAAGTAA[C/G]AGAATATAGCTGGGC	146691
rs530797989	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17948111	GAGACATTAAATGAC[G/T]GTATCATGATACAAT	146691
rs530799996	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17852088	CGGGGCTCACTTGCA[A/G]GACCCCTATTTCTAT	146691
rs530835981	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17948917	GGTGGGGGGAAAGAG[C/T]TGGAGTACAGAGCCA	146691
rs530843480	in-del	-/GAGAGGGAGA	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17913240	ACCGTGGGGAGACGG[-/GAGAGGGAGA]GGGAGACCGTGGGGA	146691
rs530855425	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17949587	TGGTCAGAGGACATA[C/T]CTCAGTAAGTGTGGC	146691
rs530885459	snp	A/G	7.51061e-05	0.00612759	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847586	GTGCCCGGTGTCCAC[A/G]GGGTGCGAGCGGGGA	146691
rs530932442	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17860230	CTCTCTAATGCCCAC[A/G]CTGGGGCAGGTGGGA	146691
rs530935930	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17897237	CGTTTTGGGCATCAC[G/T]CCTGGTTTAGTGAAT	146691
rs530967394	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17918947	ATTATAAACCCTTCT[G/T]AGGCCCCCAGGTGAC	146691
rs530969800	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17853830	GTGGAGAGGCAGGAG[C/T]AGGGGACAGAGGCCT	146691
rs530980701	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17914062	CTTCCATCAGGATAA[G/T]TCTCCTCTTGAGGAG	146691
rs530986521	snp	C/T	0.00874735	0.0655527	intron-variant	TOM1L2	GRCh38.p7	17:17962915	GCAATGAGCCGAGGT[C/T]GTGCCACTGCACTCC	146691
rs531018135	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17963410	TGCTTGATGTCTAAA[A/G]GGCAACATGAACAAA	146691
rs531041980	snp	C/G	0.00318978	0.0398085	intron-variant	TOM1L2	GRCh38.p7	17:17943490	GGAGAGAATGTGGAT[C/G]ATCCAAAAGAGAATG	146691
rs531043529	snp	C/T	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17910657	TCACTGCAACCTTTA[C/T]CTCCTGGGTTCAAGC	146691
rs531062353	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17873298	ACATTTTACAGTGAC[A/G]GCTTTAACACGTACT	146691
rs531069000	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17889695	ACTTTTCCATAATGG[A/G]AAGGTTAAGGCTGTA	146691
rs531071713	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17859795	CTGAGGCAGGACAAT[C/T]GCTTGAACCTGGGAG	146691
rs531072823	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17897989	GGAGTGCAGTGGTGC[A/G]ATCTCAGCTCACGGC	146691
rs531084801	snp	A/G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17856661	TGGAGGGAGAGGCAC[A/G/T]TGTTTGCACTGCTTT	146691
rs531128456	in-del	-/G	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17899887	GTTGAGGAGGGGAAA[-/G]GGGTTGATGCTCTGC	146691
rs531138833	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17972729	CAAATGGACGGAACA[A/G]AGGTGAATCTAGGAA	146691
rs531170053	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17892979	AATGCAACCTCAAGA[A/G]AGACTCCAAGCCAGA	146691
rs531197441	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17868449	CCTGATGAATCCAGC[A/C]GTAGGTTGTGAGTCA	146691
rs531207972	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17945346	AACTTACATTAAAAA[A/T]ATATATATGGCTCAG	146691
rs531230641	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17957137	GGAGTAGCACTACCA[C/T]ACCCAGCTAATTTTT	146691
rs531265682	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17862072	AAGGGTACATGGGAC[C/T]TTGGGTTTCTGCTTA	146691
rs531268564	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17911722	GATTTGGCAGGGTCA[C/T]AGGACAATAGTGGAG	146691
rs531275432	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17966415	GAAAGATAAAGAAAA[A/G]ATTAAAGAAACAGAA	146691
rs531296848	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17961378	TTAAGACTAGTCTGG[A/G]ATACATGGGGAGGCC	146691
rs531333462	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17856206	GCTGGATCTTCCCAA[A/T]GAATGGACATGGTTT	146691
rs531341043	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17965956	TGAAACCCTGTCTCT[A/G]CTAACAATACAAAAA	146691
rs531375655	snp	C/T	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17898018	GCAACCTCCACCTCC[C/T]GGGTTCAAGCAATTC	146691
rs531429742	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17913658	GGTTGGTTCTTTATA[A/G]TCAAAATGGGTATAT	146691
rs531438482	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17894413	ATTCAGACCCTGCCT[A/G]CTCCTCCCTTGTCTG	146691
rs531467613	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17905661	TTCCTGCCTCAGCCT[C/T]GTACAGTGCTGGGAT	146691
rs531489229	snp	A/G	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17936803	ACAGGAAGAAAATAC[A/G]CCAAAATGTTTATAG	146691
rs531534937	snp	A/T	0.00478085	0.0486577	upstream-variant-2KB, intron-variant	TOM1L2, DRC3	GRCh38.p7	17:17973642	TTTATTTATTTATTT[A/T]TTATTTTTAAAAATG	146691
rs531544382	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17848632	CTGTTTCCCAATAAG[C/T]GAGATAAATCACACT	146691
rs531567930	in-del	-/G	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17864499	CAGGCGTTAGCCACC[-/G]GCACCCGGCTTTTTT	146691
rs531580486	snp	C/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17936095	TCTGTCACTTGGCCT[C/G]GCTTGCTCCTGCCCT	146691
rs531588569	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17875466	TGTGATTCTCTTTGG[C/G]CCTAAGACACCCAAG	146691
rs531667857	snp	C/T	0.00279162	0.0372561	intron-variant	TOM1L2	GRCh38.p7	17:17849930	GGCAAGGCATGTGTT[C/T]GGAAAGCTGACCTTC	146691
rs531693919	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17930438	CTGCAGAGACCCTCA[C/T]GGTAGACAGACACCT	146691
rs531711001	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17884280	CATCAAGCCCTGAGG[C/T]GCTATGGTGCTCTGA	146691
rs531760494	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17898820	GAACAAACTGAATGT[C/G]CATCAATACACAACA	146691
rs531774849	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17920644	CGCCCGGCTTTTTTT[C/G]TTTTTCTTGAGACGG	146691
rs531781426	snp	C/G	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17906701	ACCAAGCTTGAGAGG[C/G]TGGTCCCCAGTTCAC	146691
rs531788855	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17844585	CCTTGTCCCATGCAC[A/G]CTGGTAAGCGAGCCA	146691
rs531839265	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17917581	TGGGAATACATGTGC[A/C]TGCCACCATGCCTGG	146691
rs531841157	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17953927	TGCCTTCCCTTGTAC[A/C]CTGTACAGTTAGCCA	146691
rs531845138	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17856050	AAGTTAGAGACTGGA[C/G]CTCTACGTGGGACCT	146691
rs531921572	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17951018	AAGATCCCTGGCAGG[A/T]TGTCTCCAGGGATCT	146691
rs531928276	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17892067	TTAGCAAAGCCAGTC[C/T]TGAAGACCACAAAAA	146691
rs531963124	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17953297	AAAAATATAAATAAA[C/T]AAAGGTAAATGTTAT	146691
rs531974298	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17966129	CCATCTGGAAAACAA[A/C]GAAACAAAAAAACAA	146691
rs531985273	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17951483	GGAATTTGAGTTTGT[A/G]CATAAAAAGTTGCTG	146691
rs531986037	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17901172	AAAAGCAAGTATTTA[A/T]CTCTCTCCCCGGGGG	146691
rs532050686	snp	A/T	0.00517822	0.0506191	intron-variant	TOM1L2	GRCh38.p7	17:17945296	CACACACACACTCTC[A/T]CTCTCTCTCTCTCTC	146691
rs532057096	snp	C/T	0.00159617	0.0282053	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17844056	AGACGTCCCCAAAGC[C/T]GACAGTGCAGAAGCT	146691
rs532088966	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17845805	TGAGAAACATTGAGG[A/C]GGCAGGGGCTCATCA	146691
rs532155337	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17894010	GACAGCAGCCCCTTA[C/T]TGACTGAAGTCTCCT	146691
rs532160674	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17854231	GACTCAGACTAAACA[C/T]GTACACTGCTTGGAA	146691
rs532178137	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17890328	AGCAACCTCACACCC[C/T]GGTATGAGGTGGATA	146691
rs532238510	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17923894	TGTAATCTCAGCACT[C/T]TGGGAGGTCGAGGTG	146691
rs532272097	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17916165	TGCAAGCTCTACCTC[C/T]TGGGTTCACGCCCTT	146691
rs532276747	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17960916	GACACGGAAGGTACA[A/G]GCAACAAAAGAAAAA	146691
rs532341963	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17960130	TGAGTACATAATTTA[C/G]AATACTAGTGTAGGT	146691
rs532355371	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17968795	ACTGGTACTCACAGA[G/T]GTGCCTGTGCCCCAC	146691
rs532364970	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17865276	AGATATTGACAATCA[A/T]TCAATCACAGACTTT	146691
rs532364995	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17970718	GGCTCCTAAATGCTA[A/G]TTAGCCAACAGGAGA	146691
rs532372325	snp	C/T	0.00398564	0.0444627	intron-variant	TOM1L2	GRCh38.p7	17:17917312	GCACTCCAGCCTGGG[C/T]GACAGAGCAAGACCC	146691
rs532400294	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17856933	CTGGGCTTTGTTTTC[C/T]TTTTACTCTGTTTCT	146691
rs532436762	in-del	-/C	0.00557542	0.0525036	intron-variant	TOM1L2	GRCh38.p7	17:17912990	GGAGCTGGAGACCGG[-/C]CAGGCCAACACAGCG	146691
rs532456489	in-del	-/TA	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17852164	GATCTAGGGTAAGAC[-/TA]TAAAGTAAAAATAAG	146691
rs532470721	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17955225	CTCTCCACCTCTTCT[A/G]TCATACTCAGCAGAC	146691
rs532471702	snp	A/G	0.000798403	0.0199641	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17859652	TTGGGAGGCCAAGAC[A/G]GGCAGAGTGCCTGAG	146691
rs532489904	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17849625	GGGGACTGGGGAAGA[A/G]CAGCATGTGCAGGGC	146691
rs532516304	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17877401	CTCTGTATTCTCTGC[A/C]CCGAGCACTCTGGCT	146691
rs532569690	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17915636	TCCTCCCACCTCAGC[C/T]TCCCAAGTAGCTGGG	146691
rs532613343	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17879386	TGAGCATGTATTCTA[A/C]AACTGGCATTTTATA	146691
rs532690774	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17910771	GATGGGTTTCGGCAC[G/T]TTGGCCAGACTGGTC	146691
rs532699922	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17970011	TCTTTCCACTTGCTA[C/T]ATATCCCTATATCTC	146691
rs532821952	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17898727	CCCACTTGAGGACAC[A/G]ATCCTACAGATATGT	146691
rs532824695	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17932792	CCATTTTATTGTGCA[C/T]CCGAATCATCTGTAG	146691
rs532839357	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17925462	AAAAGAAGGAAAGAG[A/G]ATATTATACAGCAAA	146691
rs532843037	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17970313	TTGTGATCCGCCCGC[C/T]TCAACCTCCCAAAGT	146691
rs532844035	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17870198	GCTCCCTGGCTGGCC[A/G]AAAGAGGAAATTCGC	146691
rs532861352	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17926121	GGCCGCAGTGAGTTG[C/T]GATCATACCACTGTA	146691
rs532878696	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17917250	GCCAGGAGAATCACT[C/T]GAACCTGGGAGGCAG	146691
rs532911630	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17903145	ACTGCACTAGTCTCC[A/G]TAGCTATATATAGCT	146691
rs532986035	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17935134	GCAAACCCTTGCCCA[C/T]AATTTCCTCAGGAAG	146691
rs532994654	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17874356	GCTCACTGCAACCTC[C/T]GCCTCCCAGGTTCAA	146691
rs533019955	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17846614	CAGGGAGCAGAGCAG[G/T]GGCCTTAGTGCTGCC	146691
rs533056793	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17929772	CCAGAGAATTACACA[C/T]ACAATTCTGCACACA	146691
rs533080647	snp	A/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17934376	CACTTGAGCCCGGGG[A/T]TCAAGGCTGCAGTGA	146691
rs533095763	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17889093	TGGTGCGGGTAAGCC[A/G]ACTGAGCCCTCGCAC	146691
rs533098012	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	TOM1L2, DRC3	GRCh38.p7	17:17972831	TTTCACCACACGGAG[A/G]TGTGGTCACGTGACT	146691
rs533122102	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17903568	CAGTGAGCCGAGATC[A/G]CGCCACTGCACTCCA	146691
rs533183945	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17943579	GCCCGAAGGCTGAGC[A/T]GCCTCCAGATCTCTC	146691
rs533221603	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17944148	ATTAACACTACTAGC[A/G]ACATAAATAATGCAG	146691
rs533231302	snp	A/G	0.00398564	0.0444627	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847033	CTGGGCTGGCAGCTG[A/G]ATGATGGAGAGAGGG	146691
rs533231938	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17941806	ATCCACAGATAACCT[A/G]TGAACCTCATTTTGC	146691
rs533255092	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17936873	TACTTCTCTACATTT[C/T]TTTCTGCTTTCAAAT	146691
rs533270731	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17942603	CAACCCTATGAGGGA[A/G]GTATTATGTCCCCCA	146691
rs533302939	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17911991	GTCACAGATCAACAG[G/T]ATCCCAAGGCAGAAG	146691
rs533309319	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17920784	GGATTACAGGCGCCC[A/G]CCACCATGCCCAGCT	146691
rs533344889	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17950379	GGCCGCGCTTGTCTC[A/G]AACTCCTGACCTAAA	146691
rs533372071	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17956636	TCCAGAGTCCTGCCC[C/T]GCAGGGAGACCGCTG	146691
rs533392339	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17868163	TGGCAAGACAAAGGG[G/T]CCTCGGGCTGGGAGT	146691
rs533403592	snp	G/T	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17848300	GGGTCTGGCAGACCT[G/T]GGGAGAGGAGGACAG	146691
rs533426371	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17854013	AACTGACTCATTACA[A/G]TATAGAAGCCACTTG	146691
rs533433172	in-del	-/T	0.0799831	0.183287	intron-variant	TOM1L2	GRCh38.p7	17:17962324	GGTGATTGTTGCATA[-/T]TTTTTTTTTTTTTAG	146691
rs533443184	snp	C/G	0.00398564	0.0444627	intron-variant	TOM1L2	GRCh38.p7	17:17912598	CGATGGGCGGCCGGG[C/G]AGAGACGCTCTTCAC	146691
rs533445708	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17953586	TGGCCCCTAACCCAG[G/T]AGGAAACCTGTGCCC	146691
rs533446733	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17904546	GAGGGGCCTGGTTGG[G/T]GTTTTTAACCTAAGT	146691
rs533474021	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17894117	TGGGATCAAAATGAC[C/T]GAGCGGTCCCTGAAA	146691
rs533514176	snp	C/T	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17891603	CCACCCTGCTGGGCC[C/T]GCCACCCTGCAGACA	146691
rs533536585	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17854685	GTGAGCCACCACACC[C/T]GCCTAATTTTTTTTT	146691
rs533540289	in-del	-/A	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17857313	GATATAAGCAACTAT[-/A]TTATAAAAATCTGTC	146691
rs533553346	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17957906	CCATCCTGGCTAACA[C/T]GGTGAAACCCCGTCT	146691
rs533559924	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17867514	CAGGCAGTGCAGGGG[A/G]AGTTGGCTTTGAGCA	146691
rs533560438	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17853021	TTAACAATGCCTAAG[G/T]CTGGCACTTCCTTGC	146691
rs533571669	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17855473	CTGATCACCAGCCAA[C/G]AGAGGCAAAAAGACC	146691
rs533597780	snp	A/C	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17860404	CGCCCTCTGGTGACC[A/C]GTGCAGAGGGATGCA	146691
rs533629586	in-del	-/TTTTTTTTTTT	0.0138799	0.0821421	intron-variant	TOM1L2	GRCh38.p7	17:17955326	AGACCACACAATTCC[-/TTTTTTTTTTT]TTTTTTTTTTTTTTG	146691
rs533640837	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17899019	TAGCACAGGTGCCAG[A/C]GTAGGGAAGAGACTC	146691
rs533647472	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17956842	AGCCCGGTTCCCGCC[A/C]GCGCCTCTCCCTCCA	146691
rs533655377	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17843824	TCTCCGGGAGAGCCT[A/G]GAGGTATGGACAGAC	146691
rs533716521	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17904928	GGCCACAGCCCTTGC[C/G]AGTCCTGCCAGGTGA	146691
rs533720049	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17905936	TGACCACTCTGCTCC[A/G]GGCCCATTAGCCACC	146691
rs533724753	snp	C/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17875502	ACTGCTTGCTCAGGT[C/G]ACCCTTTCCACTGTG	146691
rs533735756	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17898299	GGCTGGTGACAGAAA[A/G]GGGACCCACCCAAAA	146691
rs533753362	snp	C/G	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17860884	GCCGCACCCCCTCAC[C/G]GCCACAGGACACCCT	146691
rs533761273	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17965335	TTCCCAGTCTCACCC[C/G]CTATCACTCCCCTTT	146691
rs533763054	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17868609	GTCCTTCATGAAAGC[C/G]CAGTGTGCTCCCATC	146691
rs533784319	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17943798	GATCCTCAGGGTGAC[C/T]ATCTCTAACCAGCCC	146691
rs533791404	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17861587	CAAGCAGAGTTCATT[C/T]TCCTCCAGTGGTCAT	146691
rs533815458	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17848637	TCCCAATAAGCGAGA[C/T]AAATCACACTTCCCA	146691
rs533823293	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17944380	CAGGAGGCTAATTCA[A/G]TGCCTAAAAATGCTG	146691
rs533974905	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17915099	GTAAAACAAGGATAC[C/T]TCCAGCCTGTACAGA	146691
rs534010287	snp	C/T	0.0023933	0.0345097	intron-variant	TOM1L2	GRCh38.p7	17:17915741	TACCCAGGCTGATCT[C/T]GAACGCCTGGCCTCA	146691
rs534016590	snp	A/G	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17912411	GCTGCTGGGCAGAGG[A/G]GCTCCTCACTTCTCA	146691
rs534045190	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17907836	CCGTAGAGTCTGGAG[C/G]CAAACTACCTAGGTT	146691
rs534055320	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17912898	CAGCCGGGGCACCAC[G/T]GAGCACTGAGTGAAC	146691
rs534128046	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17848566	GGTGGCAATCTGCAC[C/G]CGCTATTCACCAGCT	146691
rs534132276	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17957041	AAGAGTACAGTGGCA[A/C]AATCATAGCTCGCTG	146691
rs534186339	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17959400	CTGTCAGAAATGTCA[C/T]ACATCACAGACACCC	146691
rs534225623	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17923228	CTTGATGAAATCCTG[A/G]TCTCTACTAAACATA	146691
rs534245342	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17856478	GCCCCTTGCTCCCAC[A/G]GCTCTGGGTGATCCT	146691
rs534270750	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17877392	CACTCTCAGCTCTGT[A/G]TTCTCTGCCCCGAGC	146691
rs534307863	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17930804	GTTATTGCAACTAGA[C/T]ACTAATTAGGCCCAT	146691
rs534355883	snp	A/G	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17957880	CGGATCATGAGGTCC[A/G]GAGATCAAGACCATC	146691
rs534417485	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17876697	AAGGGGGCCTGGAGA[C/T]GGCTGGTGACTTACC	146691
rs534424076	snp	A/G	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17916647	TCTTTCCTTATTCCA[A/G]TACCATGATGTTGTG	146691
rs534429905	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17929216	AGAACTGCCCATCTA[A/G]ACAGAAGTGGGCAGC	146691
rs534437025	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17969234	GCTCATTTTTGTATT[A/G]CTAGTAGAGACAGGG	146691
rs534468314	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17871445	GAGGCCGAGGCAGGC[A/G]GATCACTTGAGGTCA	146691
rs534468884	snp	A/C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17867658	AAATGCCATGGGCAG[A/C/T]GGTAGCTAAGAGACT	146691
rs534475897	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17944695	TATAAAACCAACGTC[C/T]CCTACAAGGAGAGGT	146691
rs534493772	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17952871	GGTCCTGCTGCAGGA[A/C]GGCCCCTTAGCCACC	146691
rs534531332	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17945962	CAGTCTCAACCTCCC[A/G]GGCTCAGGTGATCCT	146691
rs534573062	snp	C/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17878387	GACAAGTTGTTTCCC[C/G]GTCTATTTCCTGCAA	146691
rs534582066	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17844959	ACGGAGAGGCTGGTG[A/G]GCCTTGAGAGTCCAG	146691
rs534610962	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17879019	ATGCCCCCAGATCCA[A/T]GGGCTGTCCAGAGGC	146691
rs534625542	snp	A/G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17864384	CCTGGCTAATTTTTT[A/G/T]TATTTTTAGTAGAGA	146691
rs534665692	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17895027	AAAGTATCCTGCATA[G/T]GGGAGGTGCCCAATA	146691
rs534693570	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17952238	CTGTAAAATGAAGCC[C/T]ACAGTAGGATCCCAT	146691
rs534693727	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17851584	AGAGGCAGGCACATT[C/T]TACCATCAACAGAAA	146691
rs534707601	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17947647	GCCTTCCAGTCTGTG[A/G]TATTTTGTTATGGTA	146691
rs534714894	snp	C/T	0.00755907	0.0610114	intron-variant	TOM1L2	GRCh38.p7	17:17894940	TGTCTCAAAAACATA[C/T]ATACATACATACATA	146691
rs534728411	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17928657	TTGCTGAGGCTCATC[C/T]AGCCCCTATTGCTTG	146691
rs534731622	snp	C/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17852343	GGTGGTTTGGGGTCC[C/G]AGGTAGAGTCCAGCA	146691
rs534776941	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17963077	GATGTAAAACATAAC[A/G]ACACATTTTGCTTTT	146691
rs534803874	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17887402	CTCTCATCTCTGGGT[C/G]TCTCCCATTCATATG	146691
rs534808284	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17857087	AGCCTCCCAAGTAGT[G/T]GGGATTACAGGCACA	146691
rs534813857	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17850203	TGCACTTCTTCATCC[A/G]CCACCCTGGCCCCCT	146691
rs534847710	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17850597	AAAAGATACTGGGGG[C/G]AAGGCAAGTGTGTGT	146691
rs534876169	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17970148	CAAACTCCGCCTCCC[A/G]GGTTCAAGCAATTCT	146691
rs534908149	snp	A/C	0.000399281	0.0141238	intron-variant, downstream-variant-500B	TOM1L2, LOC100507131	GRCh38.p7	17:17858044	AGTTTAGTAACCAAG[A/C]ATCCCAACAGGATAA	146691
rs534922553	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17845401	TGGGTATGAAAAACA[C/G]TTTTGCTGGGGGCTC	146691
rs534937122	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17903825	AGGGGTTAGGGAAAT[C/G]AGATTCAAACTGAGA	146691
rs534960851	snp	C/T			intron-variant, upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17972076	AGCCCGCCCGTGAGG[C/T]GGCACAAGCGCCCGG	146691
rs534974816	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17851358	ACTATGACAGTCCGC[C/T]GTCAAGCCCAACCCA	146691
rs534993636	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17955256	AATATGGTGGTCACC[A/G]GCAGAGGGCCCTCAC	146691
rs534994226	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17965928	GAGTTTGAGACCAAC[A/G]TGGTCAACATGGTGA	146691
rs535054363	snp	C/G	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17948468	CTTGGCCAACATGGT[C/G]AAACCCCGTCTCTAC	146691
rs535095587	snp	C/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17941387	CGACTCCCTTATATG[C/G]TTGGCTTCCTTGTTT	146691
rs535110774	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17895506	TCCATAACATATGGA[A/G]TTTTATCCAATTCTC	146691
rs535133400	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17933613	GCATCATTTTGAGGG[A/C]CACCACCACACTTAC	146691
rs535153240	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17888322	TCATTCCTTTGGACC[A/G]TATACAAAACCCCAG	146691
rs535156281	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17867384	CAGGAGGAAGGCGGA[C/T]GCATGGCCCTGGCTA	146691
rs535160389	snp	A/C	0.000798403	0.0199641	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17860522	TGCTGCCTGCCTGGG[A/C]CCATTGGACAGGGGC	146691
rs535180464	snp	C/T	0.0178098	0.0926698	intron-variant	TOM1L2	GRCh38.p7	17:17912109	TTTCCCCACCTTTCC[C/T]GCCTTTCTATTCCAC	146691
rs535192696	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17904609	GGAGCAACTTGGTCG[C/T]TGTGCAGCAGGAAGG	146691
rs535227312	in-del	-/G	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17877424	TCTGGCTGCCCTCCA[-/G]GCTTGATGGAGGGTC	146691
rs535275242	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17873607	AAATACTCCCAGCAC[C/T]GGCGGCCTGATGGAA	146691
rs535307731	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17971185	AACTTAATATGAGGT[G/T]GGGGAGGAAGCAACA	146691
rs535337698	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17926406	TGAGAGCCAGTCTGG[A/G]CTGGCACAAGGGGAG	146691
rs535401417	in-del	-/T	0.0023933	0.0345097	intron-variant	TOM1L2	GRCh38.p7	17:17878459	GCCCCTAGGACTGTG[-/T]TTTGTGTCAGGCCTG	146691
rs535417304	snp	A/C	0.358728	0.225118	intron-variant	TOM1L2	GRCh38.p7	17:17867023	ATCCCTGGGACCAAG[A/C]CCAGCCAGTCCCACC	146691
rs535426678	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17866231	AAGAAAGAAAGAGAG[A/G]TGGCCTGCAAGGGAG	146691
rs535431572	snp	C/T	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17963528	TTAAGTCTCTATTTC[C/T]TCACCTGTAAGATGA	146691
rs535452826	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17882942	TACCCCACCCCATGC[A/G]GCACTTCCCCAAGGC	146691
rs535493950	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17958938	CACATAATGAAACCT[A/C]CATTAATACCCCTAA	146691
rs535504429	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17928560	GTTGCCTCCTCTCAG[C/T]GAGGGCCCCAGACGG	146691
rs535508883	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17956661	CCGCTGAGACCCGGC[A/G]AGAATTCCAGCACAG	146691
rs535578816	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17955798	CGTGTCTGGGGTTTG[C/T]TCCTTCTGATGTTCA	146691
rs535588374	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17938333	TGTGCCTAAGACCTT[A/G]CCCTCAGCAACCCAG	146691
rs535611340	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17858562	CTGGGATTACAGGTA[C/T]CTGCCACCACACCTG	146691
rs535695772	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17934512	GAAAGGCTAGCCCCT[C/G]ATACGGTAACAATGG	146691
rs535719810	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17935729	TGATGCCATCATGCT[C/T]CAAGAGCCATTAGGA	146691
rs535747836	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17943683	ACTGCCCCAGGTGGT[C/T]TGCACCAAACAGAAA	146691
rs535791693	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17962707	GCTCACGCCTGTAAT[C/T]TCAGCACTTTGGGAG	146691
rs535805763	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17890738	AAGGTGGGAGGTTTT[A/G]GGTGTGGTCATATTC	146691
rs535826508	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17948300	TACAGCTGGGGAGGG[A/C]AATAGCCCCCCAGAG	146691
rs535856970	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17875581	CCTTCTCCCATTTCT[A/G]GTCCTCAACAGAGGG	146691
rs535860441	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	TOM1L2, DRC3	GRCh38.p7	17:17974021	CCCATAGAAGAGGAC[G/T]GTTTGGGCCTTGGCC	146691
rs535876940	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17850013	GGTGTGGGAGGTAGC[C/T]AGGTCACCAGCCCAC	146691
rs535877155	snp	C/G			upstream-variant-2KB, intron-variant	TOM1L2, DRC3	GRCh38.p7	17:17973373	GTACTGTATATACCG[C/G]TTTGGATGTGAATAC	146691
rs535911441	snp	C/G			intron-variant, upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17970924	TTCAAACAAACTAAT[C/G]AGCATTCTTGACTGA	146691
rs535965442	snp	A/G	0.0209421	0.100162	intron-variant	TOM1L2	GRCh38.p7	17:17912946	CCCGGCACCTCGGGA[A/G]GCCGAGGCTGGCGGA	146691
rs535990257	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17868849	ACACCCGCCTGCTTC[A/C]CCTGAATGCTCTAGA	146691
rs535995843	snp	A/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17884379	ATGGCTCCGCCCAAG[A/T]AGCCATTTCCATGAA	146691
rs536000426	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17897568	TTCTCAAGACAGAAA[A/T]AACACCTGAAGTCGT	146691
rs536019480	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17913929	TACTTTCTTCTCCAT[G/T]AGAGTCTGTGCCACA	146691
rs536023845	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17949726	GTGTCCCGAAAAGGT[A/G]CACAGTCCAGTGGCC	146691
rs536051627	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847382	CCGCTCTTCCTGGGA[A/G]GAAACATGGGCAGAG	146691
rs536082713	snp	A/C	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17943083	CTTAGAAGCTGAGTC[A/C]TGGGTACACAGAGGT	146691
rs536090442	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17847891	AGGGCAGGCATGAAG[C/T]CCACCTAGGAGCAGG	146691
rs536118544	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17855548	TCCCTGAGAGCCGCC[C/T]GGCCCTAGCCCATTG	146691
rs536140827	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17889897	ATCCTGATACCACGA[G/T]GGTGCAGAGAAGTCT	146691
rs536185827	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17882316	GGGCCCTACATATGC[A/G]CCTGCTCTCCAATCA	146691
rs536187455	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17856049	GAAGTTAGAGACTGG[A/C]GCTCTACGTGGGACC	146691
rs536214524	snp	A/G	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17891832	GTGTCAGAGGGAGAC[A/G]GAGAGACAGAAGGAT	146691
rs536238823	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17856268	GTGGGCCAGAGGCCA[C/G]CCTGTCCCTGAAGAA	146691
rs536240949	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17944466	GCTCCCTTCACCTCC[A/C]TGGCTGCAAACCTAA	146691
rs536273880	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17857156	GACAGGGTTTCACCA[C/T]GTTGGCCAGAAGGGT	146691
rs536274980	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17908803	CAAGTGTTGGCAAGG[A/T]TATAGACAAATTGGA	146691
rs536279654	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17843878	TGATGGCTGCTCCCT[A/G]TGGCTGGTGGCCGCA	146691
rs536323729	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17878645	GACTGACAACGGAGG[G/T]CCAGACACAAATGGC	146691
rs536337613	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17940532	GTCCTGTGGGTGCAG[A/G]GCATGGAGAAGTCAG	146691
rs536355894	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17938682	CACAAACCAATACTA[C/G]CTAACCTTTACTGAC	146691
rs536359221	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17929491	ACAAAATTAGCCAGG[C/G]GTGGTGGAATGTGCC	146691
rs536364562	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17930092	AAAACAAAAAAGACA[C/T]TCCATTCTAGTTCTT	146691
rs536379219	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17901485	CTGGACCCTAGACTT[A/T]TAAGAACTCTTCCCT	146691
rs536380193	in-del	-/C			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847000	GGCTCGGCTGCTGAG[-/C]CAGCTTGGGTGTGAA	146691
rs536387059	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17881795	CGTACTCCCTGCTCA[G/T]AGCTAGCAGGGAAGT	146691
rs536417771	snp	G/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17877498	GTATTTCTCCACATG[G/T]AAGGTTGGCTGTTCA	146691
rs536434387	snp	A/G/T	0.000893426	0.0211169	missense, synonymous-codon, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17869363	TCGAAGGAAGACGTT[A/G/T]TTGAGGTCATCGTTC	146691
rs536454479	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17878126	TGTGCATCTGGGTAA[C/T]GCCTGGCCGAACCTT	146691
rs536456907	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17870196	CAGCTCCCTGGCTGG[C/T]CGAAAGAGGAAATTC	146691
rs536513446	snp	C/T	0.00279162	0.0372561	intron-variant	TOM1L2	GRCh38.p7	17:17897061	GTCCATCATGCCCTG[C/T]TAGAGGAAGGCAAGT	146691
rs536551005	in-del	-/C			intron-variant	TOM1L2	GRCh38.p7	17:17913698	CTTGAAAACTCAAAT[-/C]CCAGTAATTGAATAG	146691
rs536567710	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17906850	GTTAGTGGTATGGAC[A/G]GAGGGCTAAATACAG	146691
rs536572372	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17968433	GCACTTTGGGAGGCC[A/G]AGGAGGGTGGATCAC	146691
rs536581889	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17899096	AAGGGAACCAAAGGC[A/G]GAGGGAGGTTTTTCA	146691
rs536583333	snp	A/C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17871239	GCCGGGCGTTGGTGG[A/C/T]GGGCACCTGTAGTCC	146691
rs536589561	in-del	-/A	0.00279162	0.0372561	intron-variant	TOM1L2	GRCh38.p7	17:17933259	GGCAGGAAGAACACG[-/A]AAAGGGCCAAAGGAC	146691
rs536643807	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17968971	AGCACTTACAATCTA[C/T]ACCACTCATTGTTTC	146691
rs536651797	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17952978	CTGCCCACCACAATA[A/G]GGCTGCAATGGGGCT	146691
rs536669695	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17864555	CTTGCTCTGTTGCTC[A/T]GGCTGCAGTGCAGTG	146691
rs536692119	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17925662	GCCTGGCCAACATAG[C/T]GACCTCACCTCGTGT	146691
rs536704640	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17850691	AGCACAGTTGGCCTC[C/T]GCAGGCCGGGAGGCC	146691
rs536708059	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17946040	CGCCTGCCTGGCTAA[A/C]TTTTTCATATTTTTT	146691
rs536711661	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17865907	CCACCATGCGCAGCT[A/G]ATTTTTGTATTTTTA	146691
rs536712056	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17857644	ACCCCTGCCAGAAAG[A/C]AAGCGTGTGGCCTTG	146691
rs536735921	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17926316	GCATTTTATTCTGAC[C/G]AGGCCTCCCTGCTAA	146691
rs536778068	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17961866	AACAGAGCGAGACTC[C/T]GTCTCAAAAAAAAAA	146691
rs536819999	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17894283	GCAAATGCACACACA[A/C]ATCCCCCACTCAACC	146691
rs536834111	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17917602	CCATGCCTGGCTTCA[C/T]TGCAATTTTAACTGG	146691
rs536848971	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17946855	TCAGCCTCCCAAGCA[G/T]CTGGGACTACAGGGA	146691
rs536854548	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17894846	TGAGGCAGGAGAATC[A/G]CTTGAACCTGGGAGG	146691
rs536868884	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17967581	CACACTTCTTAGCCT[C/T]GCACACCATGGCTAG	146691
rs536896047	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17930614	CACTGCCCTGTTCCA[G/T]CCCTTTATTAACTTT	146691
rs536915512	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17946637	TAAACCACAAGTTAC[C/T]GACCCTAAGCTAGGC	146691
rs536932246	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17923847	TTGTGTCTAAAAAAG[A/G]AAAAAAAAGGCCGGG	146691
rs536933582	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17915132	TCTTCTATGTTATTA[C/T]CTGAGTATCGGCGAA	146691
rs536939646	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17887890	TTACTAAGCATCCTT[A/T]TTTTCCTACTTCAGA	146691
rs536955151	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17932188	CTTAAGTGACTTAAC[C/T]CTAGAAAATCTATGG	146691
rs536989704	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17879085	CCTGGGAATCCTCAG[C/T]GTTAGGGAAAAGCAT	146691
rs537027112	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17891681	AAGCCACCATTTGTT[C/T]TCCTAACATGAATTC	146691
rs537095847	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17865469	GCAACCTCTGCTTCC[C/T]GGGTTCAAGCAATTC	146691
rs537115633	snp	A/C	0.00199529	0.0315338	intron-variant	TOM1L2	GRCh38.p7	17:17871040	GGGAGGCTCTCCCCA[A/C]GTACTTCTGAGAGAA	146691
rs537135043	snp	C/T			intron-variant, upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17970789	TAAGCTAAAATTTCA[C/T]AAGCAAAGCAGAAAA	146691
rs537178977	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17970990	CAAGTTGCTTTCTTA[C/G]TAAGGAAGTCCCATA	146691
rs537189500	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17873270	TATGCCTATCACCTA[C/G]ATTGTACCATTAACA	146691
rs537196135	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17967015	ACTGTGGGACCTCAT[A/C]TTGTGATTGTGTGAG	146691
rs537242577	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17851124	ACAGGGCAGCCACGT[C/G]TGAGATGGCAGGTGA	146691
rs537253180	snp	C/T	0.00279162	0.0372561	intron-variant	TOM1L2	GRCh38.p7	17:17955391	GTCGCCAGGCTGGAG[C/T]ACAGTGACGACATCT	146691
rs537277318	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17845447	ATTTCAGCTTCACGC[A/G]CTATGGAATCCCTGC	146691
rs537285339	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17947567	GAGGCTTCTGAAGAA[A/G]CCAAACCTGCAGCTT	146691
rs537304654	snp	A/C	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17948537	CACGTCTGTAATCCC[A/C]GCTACTCGGGAGGCT	146691
rs537305430	snp	C/T	0.000115619	0.00760239	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17869409	TCGGTGACCTCCTCA[C/T]TGGACACGCGGGAGA	146691
rs537315458	snp	A/G	0.00199481	0.0315187	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17846119	TGAATGCTCCCCAAC[A/G]ACCATGTCGCTGGTC	146691
rs537322660	snp	C/G	0.00438332	0.0466095	intron-variant	TOM1L2	GRCh38.p7	17:17940316	TATAGCAAGAGTAAT[C/G]AATAATTGGTAGCTT	146691
rs537330010	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17945067	AATCAGGGCCGTGGA[C/T]ACCAAAATAGCTCAT	146691
rs537341485	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17908429	GACACCAAAAGCACA[A/G]GCAACAAAAGAAAAA	146691
rs537351398	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17948588	ACCCGGGAGGTGGAG[A/G]TTGCAGTGAGCTGGG	146691
rs537394280	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17887250	ACCCTTATCTGGGAC[C/T]TCTGTGCAGACTGGA	146691
rs537413024	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17896531	GGACAGAGATGCATG[A/T]GCCACAGAGCAGCCC	146691
rs537413536	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17903944	GGGGTGGGTGGGGTG[C/T]CCTACTGTCAGTCCA	146691
rs537436727	in-del	-/TT			intron-variant	TOM1L2	GRCh38.p7	17:17863563	GGGAAGACACTAGAC[-/TT]TTTTTTTTTTTTTTT	146691
rs537455379	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17867970	CACTCTAACCAGGAT[A/G]GCACTTCCAGCCACC	146691
rs537484185	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17942147	GGAGTCTAAGGAAAA[C/T]TTGTAATCCAGTTCA	146691
rs537508118	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17854588	GGTGTGCAGTGGTGC[C/G]ATCTCAGCTCACTGC	146691
rs537525243	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17881848	GCCATCCCTACACAC[A/T]CATTGCTATCCCTAC	146691
rs537542944	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17905017	CCCTGGGGGTCAGTA[A/C]ACATGGCCAGATGAC	146691
rs537546379	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17897704	AGTTTTTACCCCATG[C/T]AAAAGACCACTTTAT	146691
rs537550154	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17927039	TCTAAGTGGGTCACC[C/T]TGAATAATACGAAAC	146691
rs537586026	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17898254	AGGAAACTGATATCT[A/G]GAGAAGGAGTTGGTC	146691
rs537601508	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17972422	CCCCTCCCCACTCTC[C/T]GGAACGCCGAGCTTA	146691
rs537624314	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17881919	AGTCATGACATTGTC[A/G]CAAATAGTAAATAAG	146691
rs537625190	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17865994	TGATCCACCCACCTC[A/G]GCCTCCCATAGTGCT	146691
rs537631598	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17874062	CCGGGTTCATGACAT[C/T]CTCCTGCCTCAGCCT	146691
rs537644851	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17962604	AAGGCATGAGCCACC[A/G]CGACTGGCCCAATGT	146691
rs537666327	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17874590	TTACTTTAAAAAAAC[A/G]TTTGGAAAGTGTTAG	146691
rs537668341	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17867044	CAGTCCCACCTGGGG[C/G]CTAGGGAGTGAAACC	146691
rs537672715	in-del	-/G	0.00398564	0.0444627	intron-variant	TOM1L2	GRCh38.p7	17:17955249	AGCAGACAATATGGT[-/G]GTCACCGGCAGAGGG	146691
rs537673630	snp	A/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17859134	CAGGCCCGAGTGCAA[A/T]GGCATGATGTCGGCT	146691
rs537715056	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17946200	AATTTTGTATAAGAG[C/T]TTTATTGAGATATAA	146691
rs537774844	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17903685	TCACAGCCTTGCGGG[A/G]GTTGCAGGGCAAGAC	146691
rs537775002	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17895811	TGGTCCTTGAAATAA[C/T]CCTGTAAGATGGGAA	146691
rs537834981	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17956686	GCACAGCACTGGCGG[A/G]CCGGCACTGCTGGGG	146691
rs537837675	snp	A/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17860714	CCCTGCAAACAGACG[A/T]GCATTCATACACATT	146691
rs537847458	snp	A/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17949859	CTATTTTTTATTTTT[A/T]TTTTTTAAATTTTAT	146691
rs537895391	snp	G/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17922459	TGGTAACAGCATGGG[G/T]GCTGTAGTGGAGTGG	146691
rs537904404	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17847977	AGTCCTCCTGCCCTG[A/G]AGGGAAAGGCTCTGG	146691
rs537932259	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17923172	GAAGGCCAAGGCAGG[C/T]GGATCGCCTGAGATC	146691
rs537934066	snp	C/T	0.00636936	0.0560724	intron-variant	TOM1L2	GRCh38.p7	17:17913985	CTACTACCCCCTAGC[C/T]AGCTGGCCTCTCCCC	146691
rs537941272	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17848571	CAATCTGCACCCGCT[A/G]TTCACCAGCTCTGCA	146691
rs537971759	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17914889	TTAGGTAAAAAAAAA[A/T]TTAAAAAGAGCAGTA	146691
rs538000631	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17951007	CCACTAGGGGGAAGA[A/T]CCCTGGCAGGATGTC	146691
rs538056486	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17878135	GGGTAACGCCTGGCC[A/G]AACCTTCCTGCAGGC	146691
rs538083740	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17927705	TCTCACTCAGTCACT[C/T]AGGCTGGGAATGCAG	146691
rs538089112	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17928582	CCCAGACGGCCCCCG[C/T]GTGAGCATGCACACA	146691
rs538127224	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17937187	TTCCAGAGTTATCTG[G/T]CAGGCTATTCAACAT	146691
rs538150644	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17925352	CATATGGATAATGCC[C/T]GGAAGATAAATGGGA	146691
rs538166162	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17912214	CAGAGGGGCTCCTCA[C/T]TTCCCAGTAGGGGCG	146691
rs538173997	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17964525	TGAGGACGCACATTG[C/T]GGAGATTTTTTTCTC	146691
rs538197019	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17883713	CACTCCAGCCTGGGC[A/G]ACACAGCAAGACTCC	146691
rs538215192	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17918594	AAGCCCTGAGAAAGT[C/T]ACCTCAGACTTCTGT	146691
rs538240720	snp	G/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17945876	TTATTTTTTAAAAAA[G/T]ATGTCTATTTTTGAG	146691
rs538285614	snp	C/T	0.00119737	0.0244387	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17844945	GATTTCTAACACTCA[C/T]GGAGAGGCTGGTGGG	146691
rs538297695	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17862465	AGAAAAGAGAAAAGC[C/T]GTCTCTTACAACTGA	146691
rs538297805	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17869979	GGGCAAGCACTTCCA[C/T]AGGACAGGTTCCTTA	146691
rs538320528	in-del	-/A	0.0023933	0.0345097	intron-variant	TOM1L2	GRCh38.p7	17:17885768	CTCTACTAAAAATAC[-/A]AAAAAAATTAGCTGG	146691
rs538326344	in-del	-/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17932946	CAATATGTAAATACA[-/T]TTCCCCCTTGTAAAA	146691
rs538358633	snp	C/G	0.00279162	0.0372561	intron-variant	TOM1L2	GRCh38.p7	17:17906213	GGCTCACTGCAGCCT[C/G]GACCTCCTGGGCTCA	146691
rs538368832	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17958083	CAACAGAGCAAGACT[C/T]TGTCTCAAAAAAAAA	146691
rs538394688	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17878316	GGACTCCTCACTGGG[A/G]CTGGGCCAAGGGTAC	146691
rs538415533	snp	C/T	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17906937	AAATAACAACAGGAA[C/T]GGATCCAGCAGTGCA	146691
rs538434540	snp	A/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17943720	TCTCATCTTCCCCCT[A/T]AGTATTAAAAACCTC	146691
rs538435577	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17883203	CAAGTGGAGGGAGGG[A/C]GGTTATTAAGTTTTG	146691
rs538473216	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17944313	TCCTTCCTGACCTTG[C/G]CTGAGGCAGCCTTGC	146691
rs538482681	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17856394	ACTATGAGAGGTGGC[A/G]GGAGACCTGCCCAGG	146691
rs538513422	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17843714	AGTGGACAGCAAACG[C/T]GACATTCAACACATT	146691
rs538519833	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17850051	CAGGCTGACCCTGTG[A/G]TTAAAGAACTCAACA	146691
rs538556553	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17899851	ACCAAATGAAAAGGC[C/T]CCTTCAAATGTGTAT	146691
rs538557548	snp	C/T			upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	TOM1L2, DRC3	GRCh38.p7	17:17972874	CCCAGGATGTCTCCC[C/T]TCTGACTTCCCCTTA	146691
rs538558132	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17848268	AGTTTCCCTCCCTGC[A/G]GAGCGGTCTGGCCAC	146691
rs538568570	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17875765	TATGGATTTCCTCTG[A/G]GCCCTCCACAAGTTT	146691
rs538612111	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17893031	GAATTCCTGGCCCAC[A/T]GAAACTAAGAGATAA	146691
rs538619125	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17938153	GACTACAGGTAGAAA[A/T]GAGAGGGAGGCAGTT	146691
rs538640785	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17885175	GCCTGCCCTCTGTGC[A/G]GGAGCACCTCTGCCC	146691
rs538642052	snp	A/C			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17846009	AGCTGGAGGGCTGCT[A/C]GCCTGGCACAGGGTC	146691
rs538652952	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17953869	CAAGCAGGTGCTCTA[C/T]GCATGTTCATTGCCT	146691
rs538672755	snp	C/T	0.000798403	0.0199641	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17858386	CGCAAGTGATCCTTC[C/T]GCCTCAGCCTCCTGA	146691
rs538687020	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17851174	ATGATAAGAAGCAGG[C/T]TCCCGGCAGGGCCGG	146691
rs538703845	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17848740	CTCTGGCAGCGGGGG[C/G]TCCAAGATGATGGGG	146691
rs538730898	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17931381	TTTGGAGTCAGACCA[A/G]TTGAGCTCAAATCTG	146691
rs538735384	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17894471	GCTCAGAAAAGCCCA[A/G]CATACTGGTTCTGGC	146691
rs538785121	snp	A/G	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17894913	TCCAGCTCAGGCAAC[A/G]GAACAAAACTCTGTC	146691
rs538829460	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17863004	CAGTGCACCACATGC[C/T]GGAGGAGCCAGGGCG	146691
rs538852603	snp	A/T	0.00358779	0.0422022	intron-variant	TOM1L2	GRCh38.p7	17:17871413	GGTGCCTCATGCCTG[A/T]AATCCCAGCACTTTG	146691
rs538870576	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17969202	GCTGGGATTACAGGC[A/G]CCCACCACCACACCC	146691
rs538895922	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17864604	GCAACCTCCGCCTCC[C/T]GGGTTCAAGCGATCC	146691
rs538927939	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17850553	CCCTCCCCCAAAAAA[A/C]CAAAGCACGGCACAT	146691
rs538958845	snp	C/G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17900377	ATACAAAAAAATTAG[C/G/T]TGGGCATGGTGATGT	146691
rs538967606	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17932462	TGCCAGAAAACATAC[A/G]TCCCTTTGTTTCCTG	146691
rs538971859	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17892333	TGCCTCCCTTTGCCC[C/T]TGCTGGAGCCCCACG	146691
rs538976687	snp	C/T			downstream-variant-500B	TOM1L2	GRCh38.p7	17:17843186	TCAGGCCTGCTTGCT[C/T]AAGGCCTGGGTGCCC	146691
rs538977749	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17908794	AGAAAATAACAAGTG[G/T]TGGCAAGGATATAGA	146691
rs539000068	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17961294	AAGTGCAGGGGTTCA[C/T]GTCCTATAATCCCAA	146691
rs539018321	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17961698	CTAACACGATGAAAC[C/G]CTGTCTCTACTAAAA	146691
rs539032449	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17954469	AGGAACCCACCACCA[C/T]GTCCTGCTAATTTTT	146691
rs539084668	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17918426	AGAAGTGGTGAAAGG[C/T]AGCATCGTTGCGCCT	146691
rs539085707	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17851517	ATTTCTGAGTGGAGA[A/G]GGGAACTGGAGGAGG	146691
rs539089165	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17947600	TCTTGGATTTTCAGC[C/T]TCCAGAACTATGAGA	146691
rs539122003	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17910595	TTTTATGTGAGACAG[A/G]GTCTCACTCCATTGT	146691
rs539122299	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17902377	CACCAGGACCACAGC[C/T]TCCCATTGGTAAAGT	146691
rs539124416	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17846176	TTCCCTGCTTGGCTG[A/G]TGGTCTGGGCCGTCC	146691
rs539162538	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17911185	TTCAGGGCATCCTGG[A/C]CTGGGTCCTACCCCA	146691
rs539195349	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17955465	AGCCTCCATCTCCCA[C/T]GTAGCTGGGATTACA	146691
rs539200508	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17878976	AGGGGTAGACTGCAG[A/G]CCGCCCACTCCTGGA	146691
rs539210263	snp	A/C	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17887277	TGGATGAGATGGCTG[A/C]TAACAGAGCAGATAT	146691
rs539229860	snp	A/G	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17870079	AAAAATATGACATCA[A/G]TTTACTTACACTTCC	146691
rs539234435	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17871435	AGCACTTTGGGAGGC[C/T]GAGGCAGGCGGATCA	146691
rs539257882	snp	A/G	1.64901e-05	0.00287137	synonymous-codon, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17879666	ATCCTCCTGTCCAGG[A/G]ACCATTTCTGTTAAC	146691
rs539267263	in-del	-/GCTCATACCTGCTGT	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17923079	CAGAAGTTTCCCAGG[-/GCTCATACCTGCTGT]GCTCATACCTGCTGT	146691
rs539275208	snp	C/T	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17915916	ATCCCGCCTATTTTA[C/T]GGTTGTCTTTTCACT	146691
rs539285330	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17932461	ATGCCAGAAAACATA[C/T]GTCCCTTTGTTTCCT	146691
rs539322279	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17925917	GCCTCATGCCCATAA[C/T]CCCAGCACTTTGGAA	146691
rs539380572	snp	A/G			intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17860740	ACATTTCTTTGTTAG[A/G]CAAAAACAAAAATCT	146691
rs539398085	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17873472	CAGCCCCCATCTGCA[C/T]TCCACACAGCAGAAG	146691
rs539439435	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17934725	ATCTTATCTGGTCTT[C/T]GGGTAAAATTAAAAG	146691
rs539491682	snp	A/G	8.24436e-05	0.00641989	intron-variant	TOM1L2	GRCh38.p7	17:17866968	GGAGAGAGGATGCCT[A/G]TGATATGGCCCTGTG	146691
rs539493428	snp	C/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17859216	GAGTAGCTGGGATTA[C/G]AGGCATGTGCCACCA	146691
rs539522714	in-del	-/T	0.0023933	0.0345097	intron-variant	TOM1L2	GRCh38.p7	17:17965337	CCCAGTCTCACCCCC[-/T]ATCACTCCCCTTTGC	146691
rs539554742	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17928411	GAAATCGGCATAGGA[A/C]TGCTAAGAGGAAAAC	146691
rs539605716	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17892548	CTACAGGACCAAGCA[C/T]GCCTCCTCAGCATGC	146691
rs539643499	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17972585	GCTAGGTCACCGGAG[A/T]CCCTGTCAGCCGTGG	146691
rs539659079	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17949263	GTGTGGAACTCGTGC[C/T]AGGAAAACCCAGCTC	146691
rs539687944	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17933445	GTCAGAAAAGAAGAA[A/G]TGAGGAACAGGTATT	146691
rs539724902	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17926362	AAGGAGGTCACCCAG[A/G]GTACCCAGCTAGTTA	146691
rs539750130	snp	A/G/T	6.66327e-05	0.0057717	synonymous-codon, missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847679	GCTCTGGCTTCTTCC[A/G/T]GCCAGAAGGGTTTGA	146691
rs539768958	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17897382	AAGTTTTGGGGTTTC[C/G]CTTGGGCAAAAAATC	146691
rs539802849	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17890300	GCCCAGTGGAGCCCA[C/T]TCCCCACCACACAGC	146691
rs539818182	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17889755	CAAAAGCCAGTTTAA[C/G]TCCTTCCTGGCTGGG	146691
rs539840665	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17848021	GAGTGCTCACCCTAC[C/T]GCTGACCATTTTCCA	146691
rs539847549	snp	C/T	0.0023933	0.0345097	intron-variant	TOM1L2	GRCh38.p7	17:17935545	CCTGGTAACTGTGCC[C/T]GCTCTAGGAGGTAGC	146691
rs539945267	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17920077	TAGACGGTCCAGAGT[A/G]TTGGATGCAGCCCAC	146691
rs539973980	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17883240	ACAGATCTTTACTTG[A/G]TACCATAAGAATTAC	146691
rs539997640	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17927964	TCTTTTAGAAATGCA[C/T]ACTTAGGTATTCATA	146691
rs540021769	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17956106	AAGCCTCCCCCGCAC[A/G]AAAAAGGACCCAAGT	146691
rs540023003	snp	C/T	0.00159617	0.0282053	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17860183	GAGGGGATGTCCTCA[C/T]CAGGCAGTATCCTGG	146691
rs540032175	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17859859	GCACCCCAACCTGGG[C/T]GCCAGAGCGAGACTC	146691
rs540055823	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17853258	ATAGTCCCACACTAG[C/T]GGTTAGAGTGTGCAC	146691
rs540058953	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17962474	CACACTGCCATGCCC[A/G]GCTAATTTTTTTGTA	146691
rs540061162	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17925787	TTGAGCCCAGGAGAT[A/G]GAGGCTGCAGTAAGC	146691
rs540079197	snp	A/G	0.00318978	0.0398085	intron-variant	TOM1L2	GRCh38.p7	17:17956764	CTGCCCGGGGCCTGC[A/G]GTGCTGGGCCCGCTG	146691
rs540089545	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17923731	TTTATGTTATACACA[C/T]CTTTAAAATGGTAAA	146691
rs540092505	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847309	CCATGGGCGGGTGGA[A/G]GAAAGACAGTCCGGG	146691
rs540107304	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17851471	GGGTCTGTTTGCTCC[A/G]CTGAAGAGATTTTGA	146691
rs540114817	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17896755	TGATGTTTAAGTCCA[C/T]AAATGAAGACACAAG	146691
rs540123784	in-del	-/AAAC	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17958193	AACCTCTGTTCTTCA[-/AAAC]AAACGAACGAACAAA	146691
rs540133147	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17904715	CTTGACTACCTTTCC[A/G]GCCGGATTCCAGACC	146691
rs540210164	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17943364	GCAAAGCAGTCTCTA[C/T]AGGGGTCAGATAGTG	146691
rs540225942	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17959488	AGACCCTTTCAACTA[A/G]AGTCTTCTGATTCTT	146691
rs540269522	snp	A/T	0.0023933	0.0345097	intron-variant	TOM1L2	GRCh38.p7	17:17951320	GAGGAAACAGAATCA[A/T]ACTTCTCTGTTCTGA	146691
rs540274075	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17906277	GGGACTACAGGTGTG[C/T]ACCACCACGCCTGGC	146691
rs540327352	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17849480	CAGCCTCCTCCCGTG[A/G]CCCAGATTATATTAT	146691
rs540350191	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17899320	AACTCCTTTTCCCAG[A/G]GAAAGCTTAAGTGAG	146691
rs540359144	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17875274	AAGAAAAAAAGAAAA[A/G]AAAAAAAAAAGGACA	146691
rs540367584	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	TOM1L2, DRC3	GRCh38.p7	17:17973441	CATTGTACGACTTTG[C/G]ACAAGTTCCTTTACC	146691
rs540387211	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17891894	CCCTAGGGTAAACAG[A/G]GGAAGGCCTCCCAGA	146691
rs540411460	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17956509	CTGCACTCCTCAGCC[C/T]TTGGGCGGTCGATGG	146691
rs540413135	in-del	-/GC	0.00279162	0.0372561	intron-variant	TOM1L2	GRCh38.p7	17:17917014	AAAATACATAAATTA[-/GC]TGGGCGCAGGGGCAC	146691
rs540424546	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17956944	GCGGGCTGAAGGGCT[C/G]CTCAAGCACAGCCAG	146691
rs540461415	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17928805	CTCAGGATTTTTTTT[C/T]TCTTTAGAGCTATTC	146691
rs540479331	snp	A/C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847506	GCCTGGGAGCAGACA[A/C/T]GGTGGCATTTCCATG	146691
rs540482044	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17868999	AAAGGATCATCAAAG[A/G]AGCAGGTGCAGAAGC	146691
rs540491500	snp	C/G	0.00279162	0.0372561	intron-variant	TOM1L2	GRCh38.p7	17:17913249	GAGACGGGGGAGACC[C/G]TGGGGAGACGGGAGA	146691
rs540494858	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17942735	ACTGTTCTTATTGTC[A/G]TTACAATGGTACTAT	146691
rs540498237	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17921796	GTCTTCCTCTCGGCC[G/T]CTTCGTGCAGTCTGC	146691
rs540528180	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17905439	GTCTTATGTCAGCCA[A/G]TTCCATTGGCTCTAC	146691
rs540545266	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17915279	CAGGCTTTGCTAGCA[C/G]GTGAGACTATATCAT	146691
rs540553419	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17917202	CTGGGCGTGGTGGCG[A/C]ACACCTGTTGTCCCA	146691
rs540613057	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17855033	CCTCTGAAGATAGGT[A/G]GGCCAGGCTGGCTTG	146691
rs540617110	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17862621	CATGCTTTAAAGTTC[C/T]TGGCAGTCCTGGACA	146691
rs540651423	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17855805	CTTCCTATGTCACTT[C/T]AAGCACCACCCCACT	146691
rs540666348	snp	A/G	1.64855e-05	0.00287097	intron-variant	TOM1L2	GRCh38.p7	17:17898677	GGCATCCTTTGGCCT[A/G]GAAAAAAGAACAGAC	146691
rs540704812	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17865119	AGAGTCATATACACA[C/T]TTTGAATGTACAAAC	146691
rs540754267	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17960750	AGAGTGATAATACCT[A/G]CCTTACAGAATTGTT	146691
rs540768848	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17869800	AAATATTCCAGACAC[C/T]GTTCTCCATCACTTG	146691
rs540776788	in-del	-/A	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17871215	CTCTACTAAAAACAC[-/A]AAAAATTAGCCGGGC	146691
rs540776846	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17856744	CACAGCTTTGGGCTC[C/T]GCTAGAGGTGAAATG	146691
rs540781542	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	TOM1L2, DRC3	GRCh38.p7	17:17974175	GGCATGTTAATTAAC[A/C]TTTTTAACTAGCTTC	146691
rs540796248	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17868170	ACAAAGGGGCCTCGG[A/G]CTGGGAGTCAGGTCC	146691
rs540826135	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17937637	TCAGCTCATGAGCAG[C/T]TTTCTAAGGCTGACA	146691
rs540839507	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17919618	TCCCCATAAGTCCAC[A/G]TTTCCTGGACCCCAG	146691
rs540842853	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17965718	AAATGGAGATAATCA[C/T]AGTACCTTCCTCACA	146691
rs540864622	snp	A/C	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17938380	CTTAGACCCTTGGTG[A/C]CTTTGATTTCACTGC	146691
rs540909976	snp	A/G			intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17859549	TGTATCGCTAAGGCT[A/G]TGGCCATGGCATTGC	146691
rs540933453	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17919301	TTATTACAGCTCTTC[C/T]GAAAGGAGCTCTGCC	146691
rs540949560	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17957567	GTATGCATTTTACTA[C/T]AAGTAAACTACCTCA	146691
rs540971838	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17861909	AACACAAAGTAACAT[C/T]AATTCTTATTTTATT	146691
rs541033363	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17871109	GGTGTGGTGGCTCAC[A/G]CCTGTAATCCCAAAA	146691
rs541049729	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17923935	AAGGTCAGGAGTTTG[A/G]GACCAGCCTGGCCAA	146691
rs541060817	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17929211	AGTCAAGAACTGCCC[A/G]TCTAGACAGAAGTGG	146691
rs541073856	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17915375	ATCCTGGCTTACCAG[A/G]TGTGAAGTGGTATCC	146691
rs541110582	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17907591	AGTGGGCCTTGGCAG[A/G]AAATGGGAAGAGACC	146691
rs541131258	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17908365	TCTTAGAAGAAAACA[G/T]AGTGAAAAAACTTCA	146691
rs541148886	snp	A/C/G			intron-variant	TOM1L2	GRCh38.p7	17:17906214	GCTCACTGCAGCCTC[A/C/G]ACCTCCTGGGCTCAA	146691
rs541161194	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17879874	GGTTGCCTTTCTGAG[G/T]GCACACTGCAGAGGC	146691
rs541200240	snp	C/T	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17871961	AACTCCACAAAATAC[C/T]CACTCTCCTCTGTTG	146691
rs541207838	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17857289	CAAATCATTTTGACG[G/T]ACTTAGTGGATATAA	146691
rs541212466	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17923814	GAGACACTCCAGTCT[C/G]AGAGACAGAGCAAGA	146691
rs541220622	snp	A/T	0.117537	0.212022	intron-variant	TOM1L2	GRCh38.p7	17:17945286	CACACACACACACAC[A/T]CACACTCTCTCTCTC	146691
rs541246071	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17850748	ATGTCGGGGAGGAGG[A/G]GCAGCTATGGAGCTT	146691
rs541252707	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17844485	TCACTCACATGGAGG[C/T]GCTAATAGAAAGACA	146691
rs541256232	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17953188	AGGAGGCTGAGGCAG[C/G]AGAACTGCTTGAACT	146691
rs541305368	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17900910	ACTGCTGTCCCTGAC[C/G]CACAGCTGCCACACC	146691
rs541362021	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17935004	GGAACTCAGGGCACC[A/G]TGTGCACTGCATACA	146691
rs541374070	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17886784	AGTTGGAGGATACTT[A/C]TTCGGGTCCACTTTC	146691
rs541413034	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17845612	GGACCGCCCACCACC[C/T]GCAGGCCCAGCTCTG	146691
rs541418481	in-del	-/GAG	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17848305	TGGCAGACCTGGGGA[-/GAG]GAGGACAGGAGCACG	146691
rs541419533	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17895288	CTCAAAACGATGTCA[C/G]CAGCAACAGGGAACA	146691
rs541496894	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17926334	GCCTCCCTGCTAACT[C/G]TCCCTTGTCCCAAAG	146691
rs541501818	in-del	-/G	0.00676609	0.0577691	intron-variant	TOM1L2	GRCh38.p7	17:17939291	TTTCATCTGATGGGA[-/G]GCCTCCCAGATGGGC	146691
rs541510122	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17932590	AGCATGGCTGTATTG[C/T]TGGGGGAAAGCCAGG	146691
rs541594435	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17872722	CGCTCCAGGTGTCTG[C/T]GGAAAATCTCTGATG	146691
rs541615323	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17953985	AGCATTGTTCATCTT[C/T]GAATTCAAAATCCCA	146691
rs541630002	snp	A/T	0.00358779	0.0422022	intron-variant	TOM1L2	GRCh38.p7	17:17864891	AATAGTGGCTACAAA[A/T]ATACGAAATATTGAG	146691
rs541670727	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17947005	GCTGGGATTACAGGC[C/G]TACGCCACCGTGCCA	146691
rs541675466	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17933867	CATCCTTCAAAAGAT[A/G]ATGATCTGCCACCCT	146691
rs541685095	snp	A/G	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17909311	AGAGTCATGTTCATA[A/G]CAGCAATAGTCACAA	146691
rs541699712	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17929261	CATGCTCCACCCAGT[A/C]TGAATGTTTCTCCAT	146691
rs541775525	snp	C/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17964056	CTAGGAAGGCTGCCT[C/G]TAGGAAGAGGTGAGG	146691
rs541813529	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	TOM1L2, DRC3	GRCh38.p7	17:17973167	AGTCCTGGGCTTGTC[A/C]AGCTTTTGAATAAAA	146691
rs541837741	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17955716	GAATTGGTGGGTTCT[C/T]GGTCTCACTGACTTC	146691
rs541870640	snp	A/T	0.00478085	0.0486577	intron-variant	TOM1L2	GRCh38.p7	17:17852865	ACTGAAACTCTGTCT[A/T]AAAAAAAAAAAAAAA	146691
rs541902893	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17896122	ACCGTGAGGTAATTG[A/G]CATTCACTCTCTTGT	146691
rs541903620	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17920382	GTCTCGCTCTGTTGC[A/C]CAGGCTGGAGTGCAG	146691
rs541940416	snp	C/T	0.00318978	0.0398085	intron-variant	TOM1L2	GRCh38.p7	17:17912522	GGGGTCACGGCCTGG[C/T]AGAGGCGCTCCTCAC	146691
rs541951129	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17956803	CCCACCCAGAACTCG[A/C]GCTGGCCCGCAAGCG	146691
rs541996753	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17932284	GCTTTTTATTTCATT[A/C]TTCTTATTATTTTAT	146691
rs541999999	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17954231	GAACGGCAAAGTAAG[C/T]AGAGACCTTGGTAAG	146691
rs542005989	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17860970	CTTCTAATGGGGTTG[A/G]TACTGCTCTGCTAGG	146691
rs542014501	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17934092	GAAATCAAGACACAA[A/C]CTAGTATATTTTTTA	146691
rs542053820	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17917723	ACTTTGGGAGGCCAA[A/G]GTGGGAAGACTGCTT	146691
rs542055161	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17942420	CCCTCAATCATATCA[A/T]ATGTAAAATGGGGAT	146691
rs542055305	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17934789	ACTGTGTATGCAGGG[C/T]ACGGTGACAAGGCCA	146691
rs542150179	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17964340	CCTCTGGGCAATGTA[C/T]TTACACCGTTTTCCT	146691
rs542155962	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17858825	TGACCTCGTGATCCA[C/T]CCACCTCAGCCTCTC	146691
rs542178625	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17867361	GGCACACATAGGGTG[A/G]GCACCAGCAGGAGGA	146691
rs542197595	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17889084	CAGATCCTGTGGTGC[A/G]GGTAAGCCGACTGAG	146691
rs542206351	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17969270	CCATATTGGTCAGGC[C/T]GGCCTCCAACTCCTG	146691
rs542285833	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17956112	CCCCCGCACGAAAAA[A/G]GACCCAAGTGGGTTA	146691
rs542353193	in-del	-/A	0.00119737	0.0244387	downstream-variant-500B	TOM1L2	GRCh38.p7	17:17843162	GGCTTAGAGGGGGTC[-/A]GGGGTGGCTCAGGCC	146691
rs542356854	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17876803	CTGCTGTGCTGCTGC[C/T]CGAAGTCTAACCAAG	146691
rs542364271	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17922816	AAAGACGGAATTCCA[A/G]CGGGGAAGCAGAAGG	146691
rs542397966	snp	A/C	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17854404	CACCAGGCCCTTAGG[A/C]GGCCTCGGTATCCTC	146691
rs542409639	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17880815	TACTACACACATACG[A/G]CCCTTGTTCCTGCTC	146691
rs542430267	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17944857	TCCCAGAGATGTCTG[C/T]CTGATGGCAATGGAG	146691
rs542446425	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17873816	TGCAGAAGGCCACTG[C/T]CATGCTGCAGCGGCC	146691
rs542485807	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17939631	TGTTGAAGTTCTATA[A/G]AGGGTTTGTAGAAGT	146691
rs542505234	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17848241	TGAGAGCTAGGGAGC[A/G]GGGTCCTCTGAAGTT	146691
rs542516861	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17919608	GTAAAAAGATTCCCC[A/G]TAAGTCCACATTTCC	146691
rs542530298	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17893053	AAGAGATAATGAACA[C/T]TTTCCGTTTGAAGGT	146691
rs542536197	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17881603	CTTGGGTAGCCACAA[C/T]GAGGACCTCTTCCAT	146691
rs542551443	snp	A/T	0.00119737	0.0244387	upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17972700	ATTATTGGACAAAAG[A/T]CGAGTCAATCACGCA	146691
rs542587544	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17891442	GAGGGCAGGGTGTGC[A/G]GGGACAGGCATCCTC	146691
rs542641163	snp	A/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17936699	AGCTGTTTTTTAATT[A/T]AAAATGATTATTCTA	146691
rs542675844	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17928852	TTCAGGAAAGGCATT[C/T]CTCAGTATCAGAGAA	146691
rs542690997	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	TOM1L2, DRC3	GRCh38.p7	17:17974448	ACGATCTCGGCTCAC[C/G]GCAACCTCCGCCTCC	146691
rs542712305	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17938434	ACTGGTAACATAAGG[C/G]TGACAACAGTCCCGC	146691
rs542751102	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17892504	CTGCACACATCCCAG[C/G]TCAGAGCCCTTCGAT	146691
rs542792668	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17869597	TGCTTGTTCATAAAA[C/G]CAGACATGTGCCGAA	146691
rs542799504	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17950195	GGCGTATCACTCTGT[C/T]GCCCAGGCTGGAGTG	146691
rs542812247	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17966392	AAAACCTACATTTAA[C/T]GTTTGAAGAAAGATA	146691
rs542827880	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17943438	GCTGCCTGGAGAGTG[C/T]AGAAAAGGCCTCAGC	146691
rs542899320	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17906564	CCTGCCTCCCTACTA[C/T]TCTAGACTGGCCGCT	146691
rs542899671	snp	C/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17890375	TATTTGGCCATTTTT[C/G]ACCAACAAAGATGGC	146691
rs542900421	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17936047	TTATAGCTCCTTTAC[A/G]GTTTCCCACTGCTGT	146691
rs542902050	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17914402	ATTCTTCCTAGGCCT[A/G]CCTGCCCTCCCTTGG	146691
rs542904350	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17855855	TTTGATCTCACTCAA[C/T]AGTACAAAAAGTTTC	146691
rs542936156	snp	G/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17899417	TCTTGCAGAATTATA[G/T]ACAGTACTCAGTTCA	146691
rs542936523	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17882470	GGTGCCTCCCAGGCA[C/G]CACTCAACCCTGGGC	146691
rs542967154	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17892025	TGGGTTCTTAGGGAA[C/T]GAAGAATGAGGCAGA	146691
rs542988636	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17872708	CCTCTTTGCTCCAGC[A/G]CTCCAGGTGTCTGCG	146691
rs542989629	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17944764	ATGGAAGCCTTCCGG[C/T]GGGGAAACAGGAGGT	146691
rs543030979	snp	C/T	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17864380	CACGCCTGGCTAATT[C/T]TTTGTATTTTTAGTA	146691
rs543031410	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17848116	GGGCCAGCTTCTGAT[A/T]AAACAGGCAGGAACC	146691
rs543034065	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17953266	GCCTGGGCAACAGAG[C/T]GAGACTCTGTCTCAA	146691
rs543066372	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17850257	GCTTTGTAAAGAACA[A/G]AGGGAGGGGCCAGCA	146691
rs543100433	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17908493	ATCAAAGGACACAAC[A/G]CAGTGAACCTGCAGA	146691
rs543102639	snp	A/G			upstream-variant-2KB, intron-variant	TOM1L2, DRC3	GRCh38.p7	17:17974140	AATGAACTCTGCCAC[A/G]TGCTAAGTGTATGAA	146691
rs543127364	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17872076	ATTGCCAGGCAATAA[C/T]GGCCACAGGCGCCAA	146691
rs543127770	snp	A/C			utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	TOM1L2, DRC3	GRCh38.p7	17:17972334	GTGGACAACACGCAG[A/C]GGCCCGGGCCCCCTG	146691
rs543184530	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17861988	GGGCCTGTCACTGAT[G/T]ATGGGAGGTCTTCCT	146691
rs543246635	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17923551	TTTAATTAGCTGGGC[A/G]CAGTGGTGAGCATCT	146691
rs543311843	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17873794	TGCATTCATGAGGAA[A/G]TTTTTCTGCAGAAGG	146691
rs543319864	snp	A/C	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17924807	CTCAAATATAAAATA[A/C]AAAAGTGATGATTAA	146691
rs543326081	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17907117	GAGGCAGAGGCCAGG[A/G]AGGAGGGGAGGGACG	146691
rs543362259	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17916129	CCCAGGCTGGAGTGC[A/G]GTGGCGCGATCTCAG	146691
rs543365584	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17969304	TCAAGTGATCCACCA[C/T]CTTGGCCTCCCAAAG	146691
rs543373576	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17951419	AACATTTAGTACTTG[C/G]GTAGACACTGTAGAT	146691
rs543393560	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17905599	GCTAGAATGCAGTGA[C/T]ACCGTCCTGGTTCAT	146691
rs543393852	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17942399	GTTCATTAATCCTGG[C/G]TTTAACCCTCAATCA	146691
rs543420508	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17871691	AATAAAAATAAAATA[C/T]AAAGTATTCTGAACT	146691
rs543429750	in-del	-/AAAAAAA	0.0341387	0.126111	intron-variant	TOM1L2	GRCh38.p7	17:17869309	CAATCTTTTCAAGGG[-/AAAAAAA]AAAAAAAAGAAATCC	146691
rs543435161	snp	C/T	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17943375	TCTATAGGGGTCAGA[C/T]AGTGGCAGACCAGCC	146691
rs543455279	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17939053	GCTACTCAGTAATGG[G/T]ATGAAAAGGATAAAA	146691
rs543455770	in-del	-/AG	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17880302	ACAGGGGAAGACGAC[-/AG]GGGAGACACCTTCCC	146691
rs543457575	snp	C/T	0.00159617	0.0282053	intron-variant, downstream-variant-500B	TOM1L2, LOC100507131	GRCh38.p7	17:17858130	AAGGTTGACCAGAGC[C/T]GCTTCTCTCAATTAC	146691
rs543459051	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17864746	TGAACTCCTGACTTC[A/C]GGTGATCCACCTGCC	146691
rs543486042	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17933714	GGATATTTACTCTCA[C/T]CCTCTTTCCTTCCCC	146691
rs543488368	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17875604	ACAGAGGGAAGAACA[C/G]CTGGTCACTTGTACA	146691
rs543491855	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17908909	ATTACCCAGCCAGGC[A/G]CGGTGGCTCACGTCT	146691
rs543507901	in-del	-/T	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17968802	TCACAGATGTGCCTG[-/T]TGCCCCACTCCCTGC	146691
rs543528310	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17901086	CAGTCAGCAGCTTCC[C/T]GGATGAGGTTTAAAA	146691
rs543533492	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17970669	TGGGGTCCCTCATGC[A/G]TTATAAAAGATACTA	146691
rs543552745	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17873656	CAGTCTCCTCAACAG[A/G]GCCCTAGCCCCAGCT	146691
rs543552912	snp	C/T	0.00716266	0.059414	intron-variant	TOM1L2	GRCh38.p7	17:17865748	GTGACCTTTCTTTTT[C/T]TTTTTTTTTTTTTTG	146691
rs543589666	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17947208	TTTCAGTTTTATACG[A/G]TGGGGGGGTCTCACT	146691
rs543598559	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17962351	TTAGGGATGGAGTCT[C/T]GCTCTGTCACCCAGG	146691
rs543603823	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17954619	CGCCTGGCCCTATTT[A/G]TAAATCATTCTAAAG	146691
rs543609258	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17877798	GGAAGGAAAACGTCA[C/T]GGGAAGCAACCTATT	146691
rs543627685	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17947781	GAGCTGGGACTCAAA[A/G]TGAAGTCTGATTTTG	146691
rs543635839	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17845719	TCCCAGCCACCTTTT[C/T]TGCAGCTCAAGTGAA	146691
rs543641685	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17844991	TTTCCTGACAGAGCC[A/G]CACCCCCTTCCTGGA	146691
rs543672600	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17846285	AGCAGACTGACCCAG[C/T]GAGCTGGGCCCAAGA	146691
rs543748501	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17886846	AGACTGGAGTGGGAG[G/T]GAAATGCACACCCAA	146691
rs543764259	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17880062	CGGCTCTCCCACCAC[A/G]GGAACTTGAGTAGAA	146691
rs543767306	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17896945	AAGCGCGCTAGGATG[C/G]GGCCTCAGTGTAGGG	146691
rs543798300	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17899933	AAGAGAAACTGGGCC[A/G]GGCATGGTGGCTCAC	146691
rs543825057	in-del	-/T			intron-variant	TOM1L2	GRCh38.p7	17:17918251	CTCTAGCAGTTTTTC[-/T]TTTTTTTTTTGTTTT	146691
rs543871529	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17926114	ATGTCGAGGCCGCAG[C/T]GAGTTGTGATCATAC	146691
rs543892712	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17889519	CATCCTCAGGGCAAC[C/T]AAAGGGGCAGTGGGC	146691
rs543908162	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17917903	AAGGCTGCACTGAGC[C/T]GTAATTGAGCCACTG	146691
rs543927257	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17943244	CTGTCCCCAAATTCT[A/G]AGTCCTCTCCAATCC	146691
rs543934557	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17889918	AGAGAAGTCTGTTAC[C/T]GCTCTGGCACCCCAC	146691
rs543941103	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17971478	CTCCAAGAGCCCCTC[C/G]TCCTATCCCAGTCCC	146691
rs543984787	snp	G/T	0.000399281	0.0141238	synonymous-codon, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17866321	AAGCTGGGAGGAGAG[G/T]GAAGATGGGGGCGCT	146691
rs544009718	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17969782	ATTTACTGAGCTTCT[A/G]CTATGTTCCAGATAC	146691
rs544049797	snp	C/T	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17940852	CAGTCTCATAAATTG[C/T]TTTCTTGGCTGGATC	146691
rs544095258	snp	G/T	0.00318978	0.0398085	intron-variant	TOM1L2	GRCh38.p7	17:17963607	CACAGCACTCAGCAA[G/T]GTGCCTGGCACATGG	146691
rs544122629	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17887454	CATCCAGAGATGCCA[C/T]GTGTCCCTAGCATCT	146691
rs544125088	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17895099	TGTACACACGACGAA[A/G]GGGATGGCCTCTTAT	146691
rs544130021	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17860145	CAGGGCTGCTCCCAG[C/T]GCAGGCCAGGGTTGG	146691
rs544163483	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17911372	CCAGTCCTTGGCCAT[C/T]AGCATATCACCAGAG	146691
rs544205191	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17903937	GCACAAAGGGGTGGG[C/T]GGGGTGCCCTACTGT	146691
rs544216638	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17846962	CTCCCTGCCCAGGGA[A/G]CCTGCAGGGACCCTC	146691
rs544254104	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847488	GGTCCTGACTAGTGG[A/G]AGGCCTGGGAGCAGA	146691
rs544301635	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17957367	CACAAAAGAGCATAT[A/G]CTGTATGACTCCACT	146691
rs544320611	snp	C/G	0.0209421	0.100162	intron-variant	TOM1L2	GRCh38.p7	17:17912988	TAGGAGCTGGAGACC[C/G]GCCAGGCCAACACAG	146691
rs544330940	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17854979	AGGAAGCTAGCAGAG[A/G]AATGCCCTCCAATAG	146691
rs544334017	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17950791	TCAATACACAGAAAA[C/T]CTGTGACAGCATAGG	146691
rs544350398	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17917090	ACTTGAACTCAGCAG[A/G]CAGAGGTTGCAATGA	146691
rs544365735	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17905337	CTGATCTCTGCTCCC[C/T]AGCCTGCTCCACCTC	146691
rs544417091	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17914072	GATAAGTCTCCTCTT[C/G]AGGAGGCTGCTGGAT	146691
rs544445317	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17882366	AGAGCAGCGTCTGCA[A/T]CTCTGCATTTAAATG	146691
rs544445813	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17852996	GACGCACAAATGACT[A/G]ACAGATGTGTTAACA	146691
rs544469525	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17920587	TCGTGATCCACCCGC[C/T]TTGGCCTCCCAAAGT	146691
rs544470261	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17883192	ACCTCGGGATCCAAG[C/T]GGAGGGAGGGCGGTT	146691
rs544472096	snp	A/C	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17935773	GTCACAAGTGATGAA[A/C]TACAGTTGGCAAATC	146691
rs544480153	snp	G/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17875033	AGGCCGAGGTTGGTG[G/T]ATCACTTGAGGTCAC	146691
rs544531594	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17849173	TGGGCTGCAGAGGGC[A/G]GGACCCCACCTTTGG	146691
rs544550849	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17956356	GACACAGAGTGCTGA[C/T]TGGTGTATTTACAAT	146691
rs544558982	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17948934	GGAGTACAGAGCCAG[A/G]GCTGCTCAGAGTAAG	146691
rs544597773	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17861044	GTCCTTCCTGGTGCA[A/G]GCCATGGTTTTATCA	146691
rs544608222	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17869722	ATGTATACAAGTACA[G/T]GCTTGTACAAATCAT	146691
rs544672213	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17929333	GGTGAGAGGGGTTGA[C/T]AGGGATATTCAAGAA	146691
rs544741493	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17870294	TTAGCACTTTATGGC[C/T]TGGCTTCCATGAGCC	146691
rs544752221	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17946025	TGGGGTGCACCATCA[C/T]GCCTGCCTGGCTAAA	146691
rs544761931	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17913711	ATCCCAGTAATTGAA[C/T]AGAATGCACTGACCC	146691
rs544783375	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17943924	TTCTCTCTTCCTTGC[A/C]CATCCCTCCCCCTCC	146691
rs544790896	snp	C/T			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17843961	GGGGAGGCGAGCACT[C/T]CAGGGGCTGACAGAC	146691
rs544800441	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17951223	CCCAGTAGACGGCAG[C/T]TCCCTCGCCCACCCA	146691
rs544819091	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17944577	TCTGCTCTTGGGTGG[C/G]GAAAGAGATTCCCAT	146691
rs544831213	snp	A/C	0.000399281	0.0141238	downstream-variant-500B	TOM1L2	GRCh38.p7	17:17843362	CAGGAATTTTCCTGG[A/C]CAGGTAAGGGGCTGC	146691
rs544891008	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17912591	TCTCAGACGATGGGC[A/G]GCCGGGCAGAGACGC	146691
rs544952544	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17876303	CCAGATGAGAAGTGA[C/T]GCAGCAGGGTTTTCA	146691
rs544958163	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17868105	TAAATAGGTTTAATA[G/T]GTTAAACCCAAGCCC	146691
rs544970349	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	TOM1L2, DRC3	GRCh38.p7	17:17974120	AGTTGAGTCATGATT[A/T]GGAAAATGAACTCTG	146691
rs544982900	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17935623	CCTGGTCCCAGGGAC[A/C]CAGGGCAAGTCACCT	146691
rs544989609	snp	A/C	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17877562	TGGCTTTTGACTGCC[A/C]GGGGAAGAAGGGGTG	146691
rs545026865	snp	A/G			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847369	TGGGCCACTCTGCCC[A/G]CTCTTCCTGGGAGGA	146691
rs545089552	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17914586	CTTCCTCTCCTCCTC[C/T]ACTTTCCCCATCTTG	146691
rs545099314	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17885607	ATTATCATTTCTGTT[A/G]ACTCATGAAACTTAA	146691
rs545123910	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17886524	GCTAAGTCCTGTGAC[A/G]CCAACCTCAAAATGC	146691
rs545126728	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17915280	AGGCTTTGCTAGCAG[A/G]TGAGACTATATCATG	146691
rs545135827	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17910462	GCCCTGGCTGTACAC[A/G]AGAACCACCTGGGGA	146691
rs545173191	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17863388	AACACAACAGTGGGT[C/G]TGTAAGGATAATGAG	146691
rs545186005	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17891530	TCCCCACACAGTCAG[C/G]AGGGACAGTGCAGTT	146691
rs545205292	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17936839	ACCTTTGTGTAGTGG[A/G]ATAATGAAAATTTTT	146691
rs545207463	in-del	-/TGTTT	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17934564	AATTATGTCTTACTG[-/TGTTT]TGTTTTGTTTTGTTT	146691
rs545208745	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17878579	CAGGGCCTTCACAGG[C/T]GGCAAGCATGTGCCA	146691
rs545250973	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17857238	GATTACAGGCGTGAG[C/T]CACTGCACCCGGCCT	146691
rs545267664	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17891891	CAACCCTAGGGTAAA[C/G]AGGGGAAGGCCTCCC	146691
rs545317662	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17907327	TCAGCTTATTCGATG[C/T]CAAACCAAACATACT	146691
rs545321338	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17891869	TGGGCAGAACAGGGA[C/T]GAGGGACAACCCTAG	146691
rs545352568	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17900042	CATGGTGAAACCCCG[A/T]CTTTACTGAAATATA	146691
rs545378915	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17850698	TTGGCCTCCGCAGGC[C/T]GGGAGGCCACTGCAG	146691
rs545422622	in-del	-/A	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17905037	GCCAGATGACTGGAC[-/A]AAACAAGTGAATGAG	146691
rs545448039	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17845003	GCCGCACCCCCTTCC[C/T]GGACCAGGCAGCCTA	146691
rs545470543	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17939910	AAGAATTCTGCTTTG[A/G]GCCAGGTGTGGTGGC	146691
rs545498254	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17851376	CAAGCCCAACCCAGG[C/G]AAGGCCAAGTGACAG	146691
rs545520458	snp	A/C	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17901892	GGAAAACAGAGTCTA[A/C]AACAGTCCCAGCTGG	146691
rs545582280	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17924174	AAAAATGACTACATA[C/T]TGTATGATTCCATTT	146691
rs545604877	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17926573	ACATTTAAATGTAAC[C/T]ATATTTGGGCCTGGT	146691
rs545650271	snp	C/G	0.00199481	0.0315187	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17843982	GCTGACAGACAATGT[C/G]TCTGGGGTGGAAACA	146691
rs545692930	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17917652	ATCACTTTGGGTAGT[A/G]TTGTCATCTTAAAAA	146691
rs545697838	snp	C/T	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17900656	GCCCTGTAGGAATTC[C/T]TGGCCCCTGGGTCAA	146691
rs545718479	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17953029	AGACTGGTCCCCACC[C/T]CTTCATTTGGGAGGC	146691
rs545744089	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17971571	GAGGGTGCCCAGTCT[A/G]AGGGTTGCTGGTACC	146691
rs545756416	snp	A/T	0.0023933	0.0345097	intron-variant	TOM1L2	GRCh38.p7	17:17945298	CACACACACTCTCTC[A/T]CTCTCTCTCTCTCAT	146691
rs545793282	snp	G/T	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17865546	CAAGTCTGGCTAATT[G/T]TTTTGTATTTTTAGT	146691
rs545831641	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17858731	GGGATTACAAGCATG[C/T]GCTGCCACGCCCAGC	146691
rs545836972	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17851863	GGTTGCCTGAGCAGT[C/T]ACCTTGCTTGGGCCC	146691
rs545870938	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17849826	GCCTTGCTTCTGTGA[C/G]AGAAGCAATTTCTTT	146691
rs545882774	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17865088	AATTGGTATCATCCA[A/G]TATAACCAATGTGCT	146691
rs545892435	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17884316	AACAGGATTCCCACA[C/T]CAGATTCTAGGGGCC	146691
rs545898037	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17895133	CCCATAGGACAGGTA[C/T]GTAGCCTCTTGGAAT	146691
rs545902801	snp	C/T	0.00279162	0.0372561	intron-variant	TOM1L2	GRCh38.p7	17:17927137	TTCGGATTTTTACTG[C/T]AGAAAAATAAACACA	146691
rs545920217	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17963904	ATTTTAAGCACATTA[C/T]CTCATTTAATCGTCA	146691
rs545947289	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17879154	GGGGTGAGGTGCCAC[C/T]ACAAGGGCTCCTGTG	146691
rs545963786	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17948695	TGAAAGCAGCCCCAG[A/G]GCACAGCCTTGCTGA	146691
rs545981302	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17871878	AAACATACAGACAAG[C/T]GCTAGAATTAATAAG	146691
rs546010016	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17924999	AATATCTGGTCAGTT[A/G]AAAGTGTGTGGCACT	146691
rs546027669	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17867102	TGTGTGGGGCTCCCC[C/T]TGAGAGGATCAGCTT	146691
rs546058437	snp	A/G	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17956832	CGCCACGCGCAGCCC[A/G]GTTCCCGCCCGCGCC	146691
rs546095539	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17932975	AATATTAAAACATTA[A/C]CTTATCAGTTATGAT	146691
rs546105102	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17969505	TTTGACACTTTGTCA[C/T]AACAGTACGGAATAT	146691
rs546109574	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17846827	CCAGGACCAGGTGTG[C/T]GGGTGTGAGCCTGCA	146691
rs546143422	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17934539	ATGGCAAACATCTTA[C/G]TAGTGAGAGTAATTA	146691
rs546146235	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17881847	TGCCATCCCTACACA[C/T]ACATTGCTATCCCTA	146691
rs546166062	snp	A/G	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17970286	AGCCAAGATGGTCTC[A/G]ATCTCCTGACCTTGT	146691
rs546189790	snp	C/G/T	0.0001099	0.00741202	intron-variant	TOM1L2	GRCh38.p7	17:17866436	TGTCAGAACATGAGA[C/G/T]TGGCCATAAGCCCCA	146691
rs546222805	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17919011	GTTCCCAGCTGTCCC[C/T]GGTTCTCCCTTCAGA	146691
rs546225945	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17919997	TCCTGGTAAGCCTGG[C/T]CTTGGACCCTGATCC	146691
rs546249719	snp	A/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17918726	GGGCTCCAGCACCTG[A/T]TAGTACAGTTCACAC	146691
rs546288395	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17919423	GATTCAAAACCCTGG[A/G]AGCTCTAGCTTTCTG	146691
rs546298198	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17912065	ACTTCTTTCTACACA[A/G]ACACGGCAACCATCC	146691
rs546350399	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17919713	CCCTTAAAGCTACCA[C/T]TGAACCACTGGTCTC	146691
rs546380324	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17887535	CTGGAGTACAATGGT[A/G]GTGCCATCTCAGCTC	146691
rs546400093	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17887958	CTGAAGTGACAGTGA[A/C]AAAGGAGGGGTGCTG	146691
rs546426773	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17933920	CTTGGGCCCAAAACA[C/T]GGCTGAAGCATGAGA	146691
rs546435234	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17888256	GGCTTGGAAGACCCA[A/G]AGGAAGGTCTAATGA	146691
rs546461322	in-del	-/AAC			intron-variant	TOM1L2	GRCh38.p7	17:17923416	AAACAACAACAACAA[-/AAC]AACAACAACAACAAC	146691
rs546472285	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17889103	AAGCCGACTGAGCCC[C/T]CGCACATGTTGGTAA	146691
rs546497502	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847042	CAGCTGAATGATGGA[A/G]AGAGGGTCAAGAAGG	146691
rs546517751	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17888496	GGGAGCTTCTGTCAG[C/T]TCCTGCTTATGCCCC	146691
rs546530113	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17916468	ATAAGATAATGGTCC[A/G]ACTTCACTCTTTTGC	146691
rs546539585	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17967720	TCAAGGGATTCTTCC[A/G]CCTCAGCCTCCCGAG	146691
rs546550486	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17918192	CAACTGATTTTTGAA[C/T]GTTGATTTTGTATCC	146691
rs546556383	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17880616	CAAGAGACCAAATAA[C/T]GCTGGACAGAGGTCA	146691
rs546574206	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17943590	GAGCTGCCTCCAGAT[C/G]TCTCTTGGGGATTGC	146691
rs546607117	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17877404	TGTATTCTCTGCCCC[G/T]AGCACTCTGGCTGCC	146691
rs546611280	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17936174	CTTAGCTCCCCCAGG[A/C]GTGTGCCCTTCAGCA	146691
rs546612908	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17944168	AAATAATGCAGCCCC[C/T]GGATAGGCAGGCAGG	146691
rs546614872	in-del	-/A	0.124837	0.216412	intron-variant	TOM1L2	GRCh38.p7	17:17900522	GTAAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA	146691
rs546617516	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17935187	AAACTAATAAATACA[A/T]TAATAGGCAAGATCT	146691
rs546648436	snp	A/G	0.00835141	0.0640778	intron-variant	TOM1L2	GRCh38.p7	17:17939396	AATATATGACATTAT[A/G]AGACAACTAAAAATT	146691
rs546649635	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17936913	AAAAAGGCTTTTTAA[C/G]AGTCTAAGTTCAACC	146691
rs546668391	snp	A/G			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17845869	GCATGTGCTGCCAGA[A/G]AGGACAGGGCTAGAA	146691
rs546669609	snp	A/G	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17866981	CTGTGATATGGCCCT[A/G]TGGGGTGCTCACTAG	146691
rs546675609	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17905148	CTATTTGTGAGTCAC[A/G]TCTGTGTACCAGGCA	146691
rs546722340	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17890612	AGAATCACAGGCAAC[A/G]ATGCGTGTGACACCC	146691
rs546731783	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17848040	GACCATTTTCCAGAT[C/T]AGCACTGGGTTTTGT	146691
rs546735849	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17917072	GGCTGAGGCAGGAGA[A/G]TCACTTGAACTCAGC	146691
rs546758505	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17846618	GAGCAGAGCAGGGGC[C/T]TTAGTGCTGCCCAGG	146691
rs546783146	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17921509	GCTGGGGGAAGAGGC[C/T]AATTTAGGGCCAGGA	146691
rs546818930	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17912605	CGGCCGGGCAGAGAC[A/G]CTCTTCACTTCCTAG	146691
rs546820808	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17904552	CCTGGTTGGGGTTTT[G/T]AACCTAAGTGCCTGC	146691
rs546857785	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17904942	CCAGTCCTGCCAGGT[C/G]AGCGTTCAAGGGCAG	146691
rs546876643	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17934453	TCTCAAAAATAAAAA[A/C]CACACAAAAAAACAG	146691
rs546941880	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17958762	TGAGAGATAAGTGTC[C/T]TTTGTATGCTAATGA	146691
rs546984112	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17898171	CCTTGAGATCCTCCC[A/G]CTTCAGCCTCCCAAA	146691
rs547005157	snp	C/T			intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17860309	TTTGAGTGTCCCAGT[C/T]TCAGGGGTTCAGGTG	146691
rs547007392	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17908328	ATCAAAGACATAAAT[C/G]TAAGAGCTCAAACTA	146691
rs547029679	snp	G/T	0.000798403	0.0199641	downstream-variant-500B	TOM1L2	GRCh38.p7	17:17843436	ATGGCCACCCCTGCT[G/T]AAATAAAGCAGGTGG	146691
rs547050540	in-del	-/CT	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17867102	TGTGTGGGGCTCCCC[-/CT]GAGAGGATCAGCTTC	146691
rs547051817	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17891606	CCCTGCTGGGCCCGC[C/T]ACCCTGCAGACAGGC	146691
rs547086166	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17929532	GCTACTCAGGAGGCC[A/G]AGGCAGGAGAATCGC	146691
rs547097430	snp	C/T	0.00023076	0.010739	synonymous-codon, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17882837	GGACCTGGGCATGGT[C/T]GCAGCTGGATCCACT	146691
rs547123691	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17956644	CCTGCCCCGCAGGGA[A/G]ACCGCTGAGACCCGG	146691
rs547136211	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17883462	CCCCTGGGCCAGGTG[C/T]GGTGGCTTACGCCTG	146691
rs547181583	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17880689	AGCAACATCCAGAGC[C/T]GGACCTGAGCCTCTC	146691
rs547218631	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17854514	TTATTTATTTATTTA[G/T]TTATTTATTTAATTA	146691
rs547222349	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17854059	CCATGGTGGAGCAGG[A/G]TGATGGTTAACAGTT	146691
rs547270805	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17966037	GAGACAGGAGAATCC[C/T]TTAAACCCAGGAGGT	146691
rs547315454	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17915431	CTAATGACTACTGAT[A/G]TTGAGCATTTTTTCA	146691
rs547362311	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17854532	ATTTATTTAATTAAT[C/T]AATTTATTTAGAGAC	146691
rs547369838	snp	C/G/T	3.3172e-05	0.00407248	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17869344	CCGGCTCCCACCTCT[C/G/T]GTATCGAAGGAAGAC	146691
rs547421443	snp	C/T	3.29468e-05	0.00405861	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17898642	CGGTTCCCGTTGAGC[C/T]GCTTCTTCAGGGCTC	146691
rs547474238	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17923709	GAAAAAAGTTAAAAT[C/T]GTAGATTTTATGTTA	146691
rs547492893	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17908635	GGGAAAGGACTTCAA[C/T]AGACATTTCTCCAAA	146691
rs547497766	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17952322	CTCTGGGGAGCCTAG[C/T]TGGGCTGAGAAATTA	146691
rs547667138	snp	C/T	3.29658e-05	0.00405978	intron-variant	TOM1L2	GRCh38.p7	17:17884778	CCATGCCTGGGATAA[C/T]AGAAGGCCTGTTAGG	146691
rs547685239	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17913816	ATGGATTCTGCTGCT[A/T]AACCGAACTTGGAAA	146691
rs547721611	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17914624	GTATCAAATACTGCT[G/T]CTGTAACTGCCAGCC	146691
rs547767105	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17940272	GAGATGAGCTTATAC[A/G]GGTCAAGCACTGATA	146691
rs547779565	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17968393	GTCTTTGGGCCGGGC[A/G]CAATGGCTCACTCCT	146691
rs547800848	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17932021	AAACTACAGATAAAA[G/T]CTATCAGTTCTTGAT	146691
rs547801552	in-del	-/TCTC	0.478285	0.101912	intron-variant	TOM1L2	GRCh38.p7	17:17949839	ACTGAATCTGTTCTC[-/TCTC]TCTATTTTTTATTTT	146691
rs547827465	snp	C/T	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17857382	GAGGGCTTCCCTGAC[C/T]GGTCAGATGCTTTGA	146691
rs547834147	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17966544	TACTGAAACAGAAAC[C/T]CTGAGGGTAGGATCC	146691
rs547838508	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17933246	CAGTCTATAAAGCAG[A/G]CAGGAAGAACACGAA	146691
rs547879832	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17961560	AGCCTGGGTGACAGA[A/G]GGAGAACGTGTCTCT	146691
rs547890933	snp	C/G	0.00358779	0.0422022	intron-variant	TOM1L2	GRCh38.p7	17:17968929	CCCTGTCACCCCAGC[C/G]TCTTCTGAATTGTTT	146691
rs547895046	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17889626	GTGTTAGGGAGGCAC[A/G]TCTGTGTGGCCCCTT	146691
rs547903032	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17864501	AGGCGTTAGCCACCG[C/T]ACCCGGCTTTTTTTT	146691
rs547933186	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17925608	GCACTTTGCCACGCT[A/G]AGGTGGGAGGATCTC	146691
rs547954058	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17961080	GAGAACTCCTAAAAC[C/T]GAACAACAACAAAAC	146691
rs547957805	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17885662	GGGTGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC	146691
rs547961775	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17946417	TCTGCCTTTTCTCTA[C/T]ATAGATGTGTCTATT	146691
rs547992797	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17844686	AGCAGGCAGGCCAAA[A/G]GCCCATGGTGCCAGG	146691
rs547999511	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17948548	TCCCAGCTACTCGGG[A/C]GGCTAAGGCAGGAGA	146691
rs548025932	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17909097	GAGGCAGGAGAATGG[C/T]GTAAACCCAGGAGGC	146691
rs548026698	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17850546	CAACACTCCCTCCCC[C/G]AAAAAACCAAAGCAC	146691
rs548031367	snp	A/C	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17932729	GGCCTCAATGTTCTT[A/C]TCTATAAAATGGAGT	146691
rs548062300	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17902051	CGTGGTGGTACACAC[C/T]TATAATCCCAGCTAC	146691
rs548121945	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17891154	TCAAGGCCCTGTTCT[G/T]CTCAGGTCCCCATGG	146691
rs548123639	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17887102	CCCAGGGCGGGGTGA[C/T]CTGGACTTCTGGGAG	146691
rs548154263	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17846075	TTCCTGTTGGTGCTC[A/G]GCATGACCCCCAGCT	146691
rs548188421	snp	A/C	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17853157	CAATGACTGTAAGTC[A/C]GAATGTGTGGCCTCT	146691
rs548250929	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17856585	TGCTGGCCTTTCCTC[C/T]GGCCACAGCCTAGCA	146691
rs548260741	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17859751	CCGGCTGTGGTGGTG[A/G]GCACCTGTAATACCA	146691
rs548299884	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17879524	AACAACAGGGCCACT[A/G]GACCTGTCCCGCCTT	146691
rs548334344	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17880271	AGCACTTTTCTGCTG[C/T]GGCAAGAATGAGAGA	146691
rs548360700	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17961616	CGGTGGCTTACACCT[A/G]TAATCCCAGCACTTT	146691
rs548415636	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17851070	ACCAAAATGTACACA[A/G]AGCAAAAAAACACAA	146691
rs548415736	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17858274	TTCTTTTTCTAAACT[C/T]TTGAATACTAAATTT	146691
rs548423262	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17949507	TCTGACCTGTGCCAG[C/G]GTGGGTATATGAAAA	146691
rs548479183	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17889562	CTGGTAATCAGAGCC[A/G]TGGGTTCTACCTCTG	146691
rs548485140	snp	A/G	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17894835	ACTTGGGAGGCTGAG[A/G]CAGGAGAATCGCTTG	146691
rs548509498	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17947457	CTTTAAAGAAGTGAT[A/T]AAGTTAAAATGGGGC	146691
rs548513842	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17963290	GAAGAGAACAAAGAG[A/G]GAGCAATGGGAATCC	146691
rs548514249	snp	G/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17955341	TTTTTTTTTTTTTTT[G/T]TTTTTTTTTGTTTTT	146691
rs548558112	in-del	-/TG			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17846561	GGGAGGAGGCCAGAC[-/TG]TCAGGAGAGTCTGTG	146691
rs548573564	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17868292	GGGCACAGAGCCACT[G/T]GTGTGTACTTCCGTA	146691
rs548575400	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17918811	CCGGCTTAATGAGCC[A/G]TTAAGTATCTTCTTG	146691
rs548608049	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17910990	CCTTCTGGTGTTGGC[C/T]GCTTCTGAAGTCACT	146691
rs548647791	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17896512	CTGGTCTTGGAAGTG[A/C]CCTGGACAGAGATGC	146691
rs548678176	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17889206	GAGGGCAGCCAGAAG[A/G]CAGAAAGCCCCCATA	146691
rs548709043	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17942027	ATGTGCATGAACTTT[C/T]TATTTGAATGTTCTG	146691
rs548720865	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17897222	TTATTGAAAGCCACT[C/T]GTTTTGGGCATCACT	146691
rs548723473	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17942474	TTACTATACTAACCA[A/G]AAAATCATATCAATT	146691
rs548736625	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17921025	TCCAGATGTTATTTG[C/G]ATTTCTCCAGTTTTT	146691
rs548751588	in-del	-/TCTCTCTC	0.00801992	0.0628143	intron-variant	TOM1L2	GRCh38.p7	17:17949835	TAACACTGAATCTGT[-/TCTCTCTC]TCTATTTTTTATTTT	146691
rs548754563	snp	C/T	0.00557542	0.0525036	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847576	GGAGTGGCCAGTGCC[C/T]GGTGTCCACGGGGTG	146691
rs548766131	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17873245	AGAATTTTACAGTGA[A/C]CAGACACCATATGCC	146691
rs548767030	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17865943	GACTGGGTTTCGCCA[C/T]GTTGGTCAGGCTGGT	146691
rs548777794	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17912700	GCTCCTCACTTCCCA[C/G]ACTGGGCAGCCAGGC	146691
rs548801548	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17918089	TTGGTTAATTCCTAG[A/G]TATTTTATTTTTTTA	146691
rs548814185	snp	A/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17894041	GTCCCTGCACAATAA[A/T]CAGGCAATTAGTTGG	146691
rs548821605	snp	G/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17881294	CCAGTAGACTCTGAA[G/T]CCCTGGGTCCTCTTG	146691
rs548844926	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17861297	ATCTCACGGGGTGAG[A/G]TGAAGACTCAATGAG	146691
rs548859282	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17889674	AAGTGCTAACACATT[C/T]GATCTACTTTTCCAT	146691
rs548886160	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17942777	TCAGCACGGTAGTTA[A/G]TATAGAAAAGGAAGC	146691
rs548897117	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17874534	CCTCAGCTTCCCAAA[C/G]TGCTGGGATTACAGG	146691
rs548910167	in-del	-/A			intron-variant	TOM1L2	GRCh38.p7	17:17962960	GTGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAT	146691
rs548951073	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17881821	GAAGTGTGAGGAACA[C/T]GACACAACACTGCCA	146691
rs548965166	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17860565	AAAATTGGGACCCAG[C/T]AAGCAAACAGCCCTT	146691
rs548982942	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17929162	AGCCAGAATGCAGTC[A/G]GGACTGTGGCTGCTC	146691
rs548997874	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17912133	ATTCCACAAAACCGC[C/T]ACTGTCATCATGGCC	146691
rs548998218	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17881879	ACACACATTGCTTGA[A/C]CCCTCTGCTTCAGTG	146691
rs549061061	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17883566	AATGAAACCCTGTCT[C/T]TACTAAAAATACAAA	146691
rs549080683	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17906820	TTAAGAGGGCATGGC[C/T]ACAGTAAAGTAAGTG	146691
rs549143978	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17956919	AGGGAGGGGTTCTCA[C/G]AGTGCAGCGGCGGGC	146691
rs549155609	snp	A/C			upstream-variant-2KB, intron-variant	TOM1L2, DRC3	GRCh38.p7	17:17973831	TTCAGATCCTGTTGA[A/C]TTCAGGTTATCATTT	146691
rs549181932	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17874790	TCCCAACCCCACAGG[C/T]AGGGCCTCTATGCTC	146691
rs549182778	snp	G/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17934537	CAATGGCAAACATCT[G/T]AGTAGTGAGAGTAAT	146691
rs549219907	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17935337	ATCTGTTGGCAAATA[A/G]CAGCCTTAGCTGAGC	146691
rs549251056	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17898777	ACTATTTGCTGGCTG[A/C]AGCATGTTTGTAAAT	146691
rs549267981	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	TOM1L2, DRC3	GRCh38.p7	17:17972873	ACCCAGGATGTCTCC[C/T]TTCTGACTTCCCCTT	146691
rs549288383	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17854540	AATTAATTAATTTAT[G/T]TAGAGACAGAGTCTT	146691
rs549318887	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17936844	TGTGTAGTGGGATAA[G/T]GAAAATTTTTCTCTA	146691
rs549324525	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17952475	ACCTCACTGCAGCCT[C/T]GACCTTCCCAGGCTC	146691
rs549342664	snp	C/G	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17850028	CAGGTCACCAGCCCA[C/G]AGACAGCCAGGCTGA	146691
rs549378520	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17937741	AAGGATAAATGACAC[C/T]AAATAATGCAGAGGT	146691
rs549385910	snp	C/T	0.00358779	0.0422022	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17843666	GCCCACAGAAACACA[C/T]GACAGTGACAAAAAC	146691
rs549418132	snp	A/C	1.64844e-05	0.00287087	intron-variant	TOM1L2	GRCh38.p7	17:17850861	TCTGCCGCTCCACAC[A/C]CCACAGATGAAATAG	146691
rs549420080	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17887112	GGTGACCTGGACTTC[C/T]GGGAGACTCTGCCCT	146691
rs549433016	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17891649	AAGCTCTACCACAGG[A/G]CATGCTTTGTGAGAA	146691
rs549448146	snp	C/T	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17884262	TTTTTGACCCAAGAG[C/T]GACATCAAGCCCTGA	146691
rs549455183	snp	C/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17944290	CAAAGGGATGCTGAG[C/G]AGAGGGCTCCTTCCT	146691
rs549516431	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17945821	AGAAAAGCTAGTCAC[A/G]TAAGTCTGCCACCAC	146691
rs549525209	snp	A/G	0.000214757	0.0103601	synonymous-codon, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17869396	ATGCAGCAGCTCCTC[A/G]GTGACCTCCTCATTG	146691
rs549529107	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17877184	CACTATGGGAAGCTA[C/T]ACCCAAAAGTGCTTT	146691
rs549556109	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17957689	TATGTATATATTTAC[C/T]TGTGTGCATGTATTT	146691
rs549622073	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17930462	GACACCTGGCAGGCC[C/T]CTCCTGACACTTGGG	146691
rs549624715	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17885051	AATAACACCTATGCA[C/T]GGTGGTGCATCCTAA	146691
rs549647113	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17958859	ATCCCACCTTACCTC[A/C]GGAAAGGGGAGAGGG	146691
rs549649795	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17849008	TGTTTCCAGATTTCT[A/G]TAATAGTAAAATACT	146691
rs549651399	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17938769	AAGGTTGAAAGGGTT[G/T]TTTTTTTTTTTTAAT	146691
rs549680169	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17966921	GCTTTGCAAATTCCT[G/T]CCCTTGAACATCAGA	146691
rs549710347	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17951676	GCAAGGGGAGGCCAA[C/G]GATGCAGGAGGAACG	146691
rs549715103	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17862971	GGGAGGGTGGGGCGG[A/G]ACTTTCCTTGGTACT	146691
rs549744208	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17914794	GAGCAGGGGCTTGGA[A/G]GCACCTGGGTGGTCA	146691
rs549764985	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17865076	TCATTTGTTATAAAT[C/T]GGTATCATCCAGTAT	146691
rs549780668	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17906853	AGTGGTATGGACAGA[A/G]GGCTAAATACAGACC	146691
rs549824379	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17898944	TGTGCATAAAGTTCT[C/T]TGCATAACAGTGTAC	146691
rs549844374	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17856308	AGGCCTGGGCCAGCA[C/T]ATCTCTCTAAGAATG	146691
rs549864128	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17902132	GGTGAGCTGAGATCA[C/T]ACCATTGCACTCCAG	146691
rs549879121	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17961223	AAATCAAAACCACAA[G/T]GAGACACCAATTCAT	146691
rs549888268	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17892891	TCATCAAGGAACTGA[A/G]GCTTCCTGCCAACAG	146691
rs549911761	snp	C/T	0.000187178	0.00967234	intron-variant, downstream-variant-500B	TOM1L2, LOC100507131	GRCh38.p7	17:17857751	ACAGCAGGCTTGGCT[C/T]GGCTGGTGACTCCTC	146691
rs549934260	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17908754	ATCACCTCACACCCA[C/T]TAGGATGGCTACTAT	146691
rs549941471	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17929877	TTGGTATGAACACTT[A/G]GACAAGTTAAACACA	146691
rs549959950	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17928614	GAGATGAATTAATTG[C/T]ACTCTTCTGGGATCT	146691
rs549978487	snp	C/T	0.00438332	0.0466095	intron-variant	TOM1L2	GRCh38.p7	17:17931633	AGAAGACCTTACACA[C/T]GAGGGGACCTCAAAA	146691
rs550017751	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17910158	AGGGAGTAGCAGGGT[A/G]GGGATCAGAGATCAT	146691
rs550031482	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17967951	TACTCAGGAACTGCC[C/T]TCCAGAATAAAGGGC	146691
rs550056805	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17878226	ATATTCAGCTGGATC[C/T]GCTGAGCTGAGGCAA	146691
rs550058478	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17907657	GAGCCAACAGAGCCA[C/T]TCTAGGAGTGCTATT	146691
rs550111090	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17888862	ACAAATGGGACTTAA[G/T]GTAAGCAAACAAAAA	146691
rs550120543	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17855906	AGGAGGCTTGAAAAG[A/T]CTCAAGGTTTCTACA	146691
rs550123412	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17969951	GCCAAGAAATGGGGG[A/C]CAGGTCAAAATTCAA	146691
rs550176715	snp	A/T	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17917176	AAAAATTAAAAAATT[A/T]AAAAAATTAGCTGGG	146691
rs550189616	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17925431	TTTAAAAATTTTTTA[C/T]GTTATTACTGTTACA	146691
rs550216924	snp	C/G/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17926684	CCAACATGGTGAAAC[C/G/T]CCATCTTTACAAAAT	146691
rs550234891	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17879304	ATCAAAGCACCTACA[C/G]TGGTTATTTACAGAT	146691
rs550272756	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17850640	TACGGCTAGGACTGT[A/G]TGGGTGAAGGAGGCT	146691
rs550391828	snp	C/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17880907	CAACTTCTCTCCCCA[C/G]TGAAGCCTTTTCTGA	146691
rs550397535	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17965301	GCAAGCCCTCCACAC[A/C]ATCAGGCCTTATCCT	146691
rs550399091	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17894854	GAGAATCGCTTGAAC[C/T]TGGGAGGTGGAGGTT	146691
rs550399526	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17928266	CTGATTCTGCAAAGA[C/T]GCATAATTGAGAAAA	146691
rs550409008	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17962487	CCGGCTAATTTTTTT[A/G]TATTTTAGTAGAGAC	146691
rs550413669	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17931370	GCAGCAAGATCTTTG[A/G]AGTCAGACCAATTGA	146691
rs550418562	snp	G/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17960906	ATAAGGGCATGACAC[G/T]GAAGGTACAAGCAAC	146691
rs550439589	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17878828	AGGTCACTGCTTCTA[A/T]GGGCAGTACCACTGA	146691
rs550450935	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17924417	TGTACATTGTAAATG[G/T]GTGAATTGTATGGCA	146691
rs550477729	snp	C/T	0.00358779	0.0422022	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17858845	CTCAGCCTCTCAAAG[C/T]GCTGGGATTACAGGC	146691
rs550501452	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17880298	GAGAACAGGGGAAGA[C/T]GACAGGGGAGACACC	146691
rs550516437	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17852199	AAAAGGAATGCATAC[C/T]CCAGTGTCTATCAAA	146691
rs550522120	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17949603	CTCAGTAAGTGTGGC[A/G]TCCAAGCCTCACCTT	146691
rs550527889	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17955013	GTCTTTATGTTCAAA[A/C]AGCATTTATGGAATT	146691
rs550551120	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17903058	ATACCCTGGCACTCT[C/G]TAAGACTCCAGTCTG	146691
rs550565312	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17940359	TGCAATAAATACTAT[C/T]AGAATCATTTTACAG	146691
rs550681464	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17853884	CTCATCTGTGAAATA[A/G]GGCGATTGCTAGATT	146691
rs550705084	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17971975	GAGGTGGCACCGGCG[C/T]CCGGCGAACGCCCGA	146691
rs550723408	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17873896	TTAAACACTGCCATT[C/T]ACTGTAAAATTTTAT	146691
rs550751083	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17918965	GCCCCCAGGTGACAG[A/G]CACTGGGCAGTCTGG	146691
rs550754226	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17955143	TTGCCCAGCTGACAA[C/G]TGAGAAGACTGTGAC	146691
rs550755635	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17950572	TTCCAATACTTTGTA[C/T]GCTCCCATTCTAATG	146691
rs550788193	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17919642	ACCCCAGGAAGTGGG[A/G]CATGGGGGAGGAGGG	146691
rs550788985	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17875551	TTTCCTAAACGCTGA[C/T]GACTTCAGCTTTGGC	146691
rs550811488	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17846127	CCCCAACGACCATGT[C/T]GCTGGTCTCTTCTCC	146691
rs550841043	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17910698	TCTCAGCCTCCCGAG[C/T]AGCTGGGATTACAGG	146691
rs550845930	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17846561	GGGAGGAGGCCAGAC[C/T]GTCAGGAGAGTCTGT	146691
rs550849704	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17924000	AAAATTAGCCAGGCA[C/T]GGTGGTATGCACCTG	146691
rs550888294	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17949226	CCCAGTGCTAGGTGA[C/T]GTTCTCCAATGGGGA	146691
rs550893349	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17941141	TAAGAAAGGCTTCTA[C/T]GTTTGCTAACTGCCC	146691
rs550927074	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17869193	TTTTTCCTGTCAGCC[A/G]GGAACAAATTAGCAT	146691
rs550933246	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17861410	GAATTACCCAGCCAG[C/T]TTTGCCAAACCACCT	146691
rs550957326	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17911761	AGCAGATAAACAAGT[A/G]AACAAAGGTCTCTGG	146691
rs550965747	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17862082	GGGACCTTGGGTTTC[C/T]GCTTACCCTACTGAG	146691
rs550991906	snp	C/T	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17904516	GGAGCTGCCGAGGGG[C/T]CTGGGGCTCCTCATG	146691
rs551007637	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17848258	GGTCCTCTGAAGTTT[C/G]CCTCCCTGCGGAGCG	146691
rs551037014	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17956618	GGCATGGTGAGCTGC[A/G]GGTCCAGAGTCCTGC	146691
rs551063228	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17965980	ACAAAAATTAGCCGG[A/G]CATGATGGTGGGCAC	146691
rs551079172	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17881940	AGTAAATAAGGATTT[A/G]GTAAATATAAACATT	146691
rs551080880	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17889719	GGCTGTACCCCACTC[C/T]ACCCCCAAGCCACAA	146691
rs551089899	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17961568	TGACAGAAGGAGAAC[A/G]TGTCTCTTAAAAAAA	146691
rs551091670	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17935458	ATGGCAGAAAAGTGA[A/C]CTTCTCCACATCCTC	146691
rs551101860	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17877211	CTTTGCGATGTGCAG[A/G]AGGCAACCGGGACAT	146691
rs551119621	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17890583	CTTGGCACAGCAATG[G/T]CAACGAAAGACCTAG	146691
rs551128453	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17963449	CTGGAGCTAGAGCCC[C/T]TGGCTGGAGAGGACC	146691
rs551160408	snp	C/T	0.00019772	0.00994086	intron-variant	TOM1L2	GRCh38.p7	17:17866850	TCTGGCCTCAGGAGA[C/T]GACAGGATTCTGAAG	146691
rs551168869	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17972756	GGAATATCCCCGCCC[A/G]TAGAAAGTACTGATT	146691
rs551189977	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17898847	AACAGGTTAAATTAA[A/G]TCATTGACACAATGG	146691
rs551197665	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17867444	CTACAGAGAGGCCTG[G/T]GCCAGTCATCGAAGG	146691
rs551221262	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17903715	CAGACACTAACAACC[A/G]TCCCACAGATCTGTA	146691
rs551229094	snp	C/T	0.00358779	0.0422022	intron-variant	TOM1L2	GRCh38.p7	17:17855403	GTTTTGACTTAGATT[C/T]TCTCACATGAGGATA	146691
rs551240043	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	TOM1L2, DRC3	GRCh38.p7	17:17973643	TTATTTATTTATTTT[C/T]TATTTTTAAAAATGG	146691
rs551249288	snp	G/T	1.64811e-05	0.00287059	synonymous-codon, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17882747	AGTCACACTCAGAGC[G/T]GGGGCCTGCGGTGCG	146691
rs551263823	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17936113	TTGCTCCTGCCCTGT[C/T]TTCCTCTGCAGCCCA	146691
rs551297398	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17868532	CTGTCCTGTCCTCTC[A/G]AGCCTCATCTTTAAG	146691
rs551300504	snp	C/T	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17928291	AGAAAAACACTGCTG[C/T]TCCCAACAAACGAGA	146691
rs551338699	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17860270	AAGTAATGGGAGAAT[C/T]AGAGCCATGAGCACT	146691
rs551375287	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17923177	CCAAGGCAGGCGGAT[C/T]GCCTGAGATCAAGAG	146691
rs551389835	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17912863	AGGTTGTAGCGAGCC[A/G]AGATCATGCCACTGC	146691
rs551412122	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17923658	TCGCACCACTGCACT[C/G]CAGCCTGGGCAAGAG	146691
rs551413396	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17958535	TCCATTAAAATGACA[G/T]ACTTACTACCCCATG	146691
rs551416764	in-del	-/GC	0.00279162	0.0372561	intron-variant	TOM1L2	GRCh38.p7	17:17906209	TCATGGCTCACTGCA[-/GC]CTCGACCTCCTGGGC	146691
rs551420806	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17913685	ATATATCTTTTAGCT[C/T]GAAAACTCAAATCCC	146691
rs551445730	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17877219	TGTGCAGGAGGCAAC[C/T]GGGACATAACCTGCC	146691
rs551456473	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17906714	GGCTGGTCCCCAGTT[C/T]ACACATGGCAAGGCT	146691
rs551555530	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17921032	GTTATTTGGATTTCT[C/T]CAGTTTTTCCAATAA	146691
rs551598972	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17891739	GCCCCAGAAGGAAGG[A/G]CTGTGGTAGAGTGGG	146691
rs551606814	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17928950	CAAAATCAAGCAGAC[C/T]TTCTGTCTAGATCCT	146691
rs551652880	snp	C/T	0.00557542	0.0525036	intron-variant	TOM1L2	GRCh38.p7	17:17921325	TTAGCCACACAGGCC[C/T]GAGGCTGCTGACCCA	146691
rs551664079	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17849106	TAGGTTTTGATCCTC[C/T]AGAAAGGCTGGAAAG	146691
rs551671147	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17881114	GCACAGAGACAGGGA[C/T]AGGAGACCTCAATCA	146691
rs551679814	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17884286	GCCCTGAGGTGCTAT[G/T]GTGCTCTGAGGGACA	146691
rs551680207	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17876236	CAGTGTCTTGAATTT[C/T]GGGCCCAGACCTAAG	146691
rs551694085	snp	C/T			upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	TOM1L2, DRC3	GRCh38.p7	17:17972886	CCCTTCTGACTTCCC[C/T]TTAGCAACCAAGTCG	146691
rs551759017	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17940077	GGGTGCCTGTAATCC[C/T]AGCTGCCTGAGAGGC	146691
rs551892205	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17940181	CTGGGCGACAGAGCA[A/C]GACTCTATCTCAAAA	146691
rs551930285	snp	C/T	0.00318978	0.0398085	intron-variant	TOM1L2	GRCh38.p7	17:17891955	CATTATAAAGAAATA[C/T]TGAACACCCGCTCTA	146691
rs551930578	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17856057	AGACTGGAGCTCTAC[A/G]TGGGACCTGGCAGTG	146691
rs551946414	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17931418	CTGCTTATATGCTGT[A/G]TGATCCTAACCAAAT	146691
rs551966162	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17951493	TTTGTGCATAAAAAG[C/T]TGCTGCCCTGGAGTG	146691
rs551967351	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17849760	GGACACATCCCCTCC[C/T]TGTCTGGACCCTGGG	146691
rs551991637	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17899560	ACATATTACATGTAG[A/G]TCTTGTGTCTAACAT	146691
rs552090204	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17922048	CTTCCCAGCTCAATT[G/T]AAAAACTTCAACTGT	146691
rs552104380	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17846442	AGACACACCAGTGAG[G/T]ACACGGGATGGGAAT	146691
rs552106308	snp	C/T	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17962453	GAGTACCTGGGACTA[C/T]AGGCGCACACTGCCA	146691
rs552118091	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17907725	GGCTGATGTTATAAC[A/G]AGGTTCTTCATTCAC	146691
rs552122753	snp	C/G	0.000798403	0.0199641	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17858394	ATCCTTCCGCCTCAG[C/G]CTCCTGAGTAGCTAG	146691
rs552133455	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17850998	GCCCCCACACAGCCA[C/G]CGAGGGGAGACAGAA	146691
rs552138706	in-del	-/AAAA	0.00478085	0.0486577	intron-variant	TOM1L2	GRCh38.p7	17:17852864	ACTGAAACTCTGTCT[-/AAAA]AAAAAAAAAAAAAAA	146691
rs552153041	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17900404	ATGTGTGCCTGTAGT[C/T]CCAGGTACTCTGGAG	146691
rs552163227	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17886791	GGATACTTCTTCGGG[C/T]CCACTTTCTAAGGCA	146691
rs552170240	snp	A/G	0.0023933	0.0345097	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17845356	CCAGCTGGCGCTGGC[A/G]CTGGAGCTGGAGCGG	146691
rs552280861	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17894770	GCCCTGCGTCTACTA[C/T]AAATACAAAAACTAG	146691
rs552284863	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17886121	CACAGAATTTAACTG[C/T]CTCCCTCACTCCAGC	146691
rs552323480	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17886975	GCCATGTGCCAGCAC[A/C]GGACTGGAAGCAGAG	146691
rs552352287	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17968796	CTGGTACTCACAGAT[A/G]TGCCTGTGCCCCACT	146691
rs552362910	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17960926	GTACAAGCAACAAAA[G/T]AAAAAGTAGAGAAAC	146691
rs552365287	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17915745	CAGGCTGATCTTGAA[C/T]GCCTGGCCTCAAGTG	146691
rs552372801	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17863870	ACACTTTTGTTGTTG[C/T]TGTTGTTTTGTTTGA	146691
rs552394044	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17903592	CACTCCAGCCTGGGC[A/G]ACAGAGCGAGACTCC	146691
rs552398859	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17965062	AGTGTCCCTACCCTT[A/G]ACCACAGCTGACATC	146691
rs552437504	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17947110	GGACAATCCCACACA[A/G]TAAATACAATCTTCA	146691
rs552448932	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17901182	ATTTATCTCTCTCCC[C/T]GGGGGAAAAGCTTCA	146691
rs552471026	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17953428	ATTCCTGTAAGGTGC[C/T]AGAGACAAGCAGGAG	146691
rs552489013	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17865280	ATTGACAATCAATCA[A/G]TCACAGACTTTTCTA	146691
rs552544408	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17918432	GGTGAAAGGCAGCAT[C/T]GTTGCGCCTATATAT	146691
rs552555707	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17955228	TCCACCTCTTCTATC[A/G]TACTCAGCAGACAAT	146691
rs552574116	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17945880	TTTTTAAAAAAGATG[C/T]CTATTTTTGAGACAA	146691
rs552583160	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17910607	CAGAGTCTCACTCCA[C/T]TGTGCAGGCTGGAGC	146691
rs552597743	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17918038	AATTTCTTTCAGCAA[C/T]GTTTTATAGTTTTCG	146691
rs552620471	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17911203	GGGTCCTACCCCAGG[C/T]GAGAGAAAATGCCAT	146691
rs552632937	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17873162	CTTACTCATCCTTCA[A/G]GGCCTCAGGATGTTT	146691
rs552635003	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17961708	GAAACCCTGTCTCTA[A/C]TAAAAATACAAAAAT	146691
rs552683363	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17852261	AAGAACAAAGAACAC[A/G]TATCACCAGCAGTGA	146691
rs552740187	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17947588	CCTGCAGCTTGATCT[C/T]GGATTTTCAGCCTCC	146691
rs552752349	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17948255	CCAAGATAAATACGC[C/T]CTAGTCCCTACCTTG	146691
rs552753764	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17945584	CATTAAACTTCCTTA[C/T]CACATACATACCCAT	146691
rs552793390	snp	G/T	1.64936e-05	0.00287168	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17879688	TCTGTTAACATCTCA[G/T]ACATGACTTTTGTGT	146691
rs552832416	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17880362	CCCTTGAAAAATACC[C/T]AAGTTGCCCATCAGC	146691
rs552833210	snp	C/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17872153	AAACCAACAACACAG[C/G]GGAAACACTCATTAC	146691
rs552858309	snp	A/C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17917251	CCAGGAGAATCACTC[A/C/G]AACCTGGGAGGCAGA	146691
rs552882386	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17867854	GTTTTTTCAACAGTG[G/T]TCTACAAGGAGAACA	146691
rs552913408	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17933463	AGGAACAGGTATTGG[C/G]AGCCTGTGGAACAGT	146691
rs552932414	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17948542	CTGTAATCCCAGCTA[C/G]TCGGGAGGCTAAGGC	146691
rs552935115	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17935665	CTCTATGGGATCCAA[C/T]GCAAAGCTGAATTAT	146691
rs552988292	snp	A/T	0.00716266	0.059414	intron-variant	TOM1L2	GRCh38.p7	17:17952711	ATATTTTATAATTTT[A/T]AAAAACAAAAATGGG	146691
rs553012262	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17955631	GGCATAAGCCACTGC[A/G]CCCAGCCTCTTCTTT	146691
rs553020848	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17908922	GCGCGGTGGCTCACG[C/T]CTGTAATCCCAGCAC	146691
rs553027139	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17930608	TCACATCACTGCCCT[A/G]TTCCAGCCCTTTATT	146691
rs553032270	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17878781	GTGTGTGGGGCCTTG[C/T]AGTTCACAGCATCCT	146691
rs553040771	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17896110	CTGATTCTGGTAACC[A/G]TGAGGTAATTGGCAT	146691
rs553041426	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant, utr-variant-5-prime	TOM1L2, DRC3	GRCh38.p7	17:17973021	CTTGCAGGGACAGAT[A/G]GTGCCCGACGTAACT	146691
rs553055524	snp	A/G	0.00398564	0.0444627	intron-variant	TOM1L2	GRCh38.p7	17:17964729	ACTGCATTCCAGCCT[A/G]GGCGACAAAGCAAGA	146691
rs553083366	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17963469	TGGAGAGGACCGCTC[C/G]GCCTACTTGAGCCAG	146691
rs553084549	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17904718	GACTACCTTTCCAGC[C/T]GGATTCCAGACCCTC	146691
rs553099640	in-del	-/A	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17907348	AAACATACTAGGAAC[-/A]AAAACAAAAAATAAA	146691
rs553101920	snp	A/G	0.00119737	0.0244387	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17859311	AACTTCCGACCTCAC[A/G]TGATCCGCCCGCCTC	146691
rs553117396	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17927897	CAAAGTGTTGGGATT[A/G]CAGGCATGAACCACC	146691
rs553140705	snp	A/C	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17859861	ACCCCAACCTGGGCG[A/C]CAGAGCGAGACTCCA	146691
rs553140823	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17852800	AACCTGGGAGGCAGA[C/G]GTTGCAGTGAGCCGA	146691
rs553148438	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17920174	AGAGTGCTGGTGAAA[A/G]TGTCAAGTTAAATTA	146691
rs553155612	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17925994	TGGGTAACACAGCAA[C/G]ACCTTGTCTCTACCA	146691
rs553174899	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17874718	AACATCTGCTCTGGC[C/T]TTGTGTTTGCTGCCT	146691
rs553178637	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17868619	AAAGCCCAGTGTGCT[C/T]CCATCAGGTGATGAG	146691
rs553213523	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17868026	TGTGTAATGCTTGGA[C/T]TGGGAGACTCTTGGG	146691
rs553253311	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17865655	AAATGCTGGGATTAC[A/G]CGCCCGGCCTTGACC	146691
rs553262702	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17949273	CGTGCCAGGAAAACC[A/C]AGCTCACCATCCACG	146691
rs553301450	snp	A/C/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847322	GAGGAAAGACAGTCC[A/C/G]GGTGGTCTGCTCAGG	146691
rs553362126	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17849262	CACACACAGGGTCAC[A/G]TGTGCCCAACACAAC	146691
rs553429875	snp	A/G	0	0	intron-variant	TOM1L2	GRCh38.p7	17:17883245	TCTTTACTTGGTACC[A/G]TAAGAATTACTTTTT	146691
rs553448714	snp	C/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17882099	TTTATCAGGAAGTAA[C/G]CCGGGAGGGTGGGGA	146691
rs553511395	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17860889	ACCCCCTCACCGCCA[C/G]AGGACACCCTCCCAG	146691
rs553533021	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17891400	GGAAAGTGTGGAGGG[G/T]TGATCCTGATAGGAA	146691
rs553559585	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17891994	ACTGCTCTAGACCCT[A/G]GGGACAGCATGTCCC	146691
rs553577557	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17853269	CTAGCGGTTAGAGTG[C/T]GCACCAGCCCTTTCT	146691
rs553620760	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17925632	GGATCTCTTGAGCTC[A/C]GGAGTTCAAGACCAG	146691
rs553630879	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17957052	GGCACAATCATAGCT[C/T]GCTGCAGTCTCCACC	146691
rs553648938	snp	C/T	5.01333e-05	0.00500641	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17861590	GCAGAGTTCATTTTC[C/T]TCCAGTGGTCATGGA	146691
rs553683004	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17889395	CAGGCAGATATGCAC[A/G]GATGAGCTCTATCAC	146691
rs553684106	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17951128	CCCTGAGAGGCTTCT[A/G]GGATGTCAATCAGCC	146691
rs553685655	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17854744	TTGCCATGTTGGCCA[C/G]GCTGATCTCAAACTC	146691
rs553737638	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17944394	AGTGCCTAAAAATGC[G/T]GTAACAGTTTCTTTG	146691
rs553772713	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17943848	CTTGCCAGGGCCCCA[C/T]GTGAACATCCAGAGC	146691
rs553774309	snp	C/T	0	0	intron-variant	TOM1L2	GRCh38.p7	17:17899035	GTAGGGAAGAGACTC[C/T]CTAGAAAGAGCTATA	146691
rs553791494	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17898308	CAGAAAAGGGACCCA[C/T]CCAAAACCTTTAGCT	146691
rs553809541	snp	C/T	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17936537	ATATAAGCCCTAAGA[C/T]GTTTATCACTGCATT	146691
rs553813185	snp	C/T	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17891780	AAGGTAAAGTGCATG[C/T]ACACGTGTGTGTGTG	146691
rs553857488	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17900539	AAAAAAAAAAAAAAA[A/T]GAGAGAAAGAAAGAA	146691
rs553880485	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17843844	TATGGACAGACAGAA[A/G]CAGTTCTGACTCGGG	146691
rs553890199	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17868677	CCTATTTAAAACTAG[A/G]TCTAAATAAGACATT	146691
rs553904062	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17876719	TGACTTACCTGGCAT[C/T]GCCCAGCTCATCAGT	146691
rs553956221	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17951934	TCTGTTGGTGAGGGG[C/G]TCATTTAGAGGGCAA	146691
rs553956533	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17937304	TATTCAAGGAACACC[A/G]ACATTTTTATTTTTA	146691
rs553984572	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17892466	CCTTCTGTGTCACCA[C/T]GTGCTCTGTCTAAAA	146691
rs554003861	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17912436	TTCTCAGACGGGGCG[C/G]TTGCCAGGCAGAGGG	146691
rs554036850	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17877418	CGAGCACTCTGGCTG[C/T]CCTCCAGCTTGATGG	146691
rs554042385	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17912913	TGAGCACTGAGTGAA[C/T]GAGACTCCGTCTGCA	146691
rs554078560	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17905180	CAAGCTGATCACCTA[C/T]ATTTAGCTGGTGAAA	146691
rs554091579	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17922731	AAACAGGGAACCTGG[A/G]ACATAGTGAGGGCGC	146691
rs554128727	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17931469	CAGTTTCCACATCTA[C/T]AGAACAGAAACAGGG	146691
rs554178812	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17959410	TGTCATACATCACAG[A/T]CACCCTCTCTGGCCT	146691
rs554211504	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17856507	CTGCATGGCCCAAGT[G/T]CCTACTCACTGGTCA	146691
rs554251190	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17924030	GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG	146691
rs554276021	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17919544	GGCACACCACAATTT[C/T]CTTAAGAATCCAAGC	146691
rs554284725	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17952928	CTGACAGAACAGGAA[G/T]GTTGAAAAGGTGTAT	146691
rs554322795	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17901577	CTTCAGGACTACTCT[C/T]TGGAAAAGCTTTCTC	146691
rs554342427	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17857102	TGGGATTACAGGCAC[A/G]TGCCACCACACCCAG	146691
rs554346604	snp	C/T	0.0023933	0.0345097	intron-variant	TOM1L2	GRCh38.p7	17:17850218	GCCACCCTGGCCCCC[C/T]ACTGGGCTGCTGAGA	146691
rs554361020	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17848734	TAGGTGCTCTGGCAG[C/T]GGGGGCTCCAAGATG	146691
rs554362914	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17896393	AGCAGCCTGGGGCTC[C/T]ACTCCACTCTCAGAG	146691
rs554374172	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17883268	TACTTTTTTGGTCTT[C/T]ACAAGTAGACTAATA	146691
rs554426431	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17930035	CCTGGGCACACACAG[A/G]AAGGCAAGAGCACCA	146691
rs554443321	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17844486	CACTCACATGGAGGC[A/G]CTAATAGAAAGACAG	146691
rs554444677	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17870672	TATTCACAGGAGACA[C/T]GGCAATCTCTCTTTA	146691
rs554465263	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17955780	TACAGTTCTTAAAGG[C/T]GGCGTGTCTGGGGTT	146691
rs554478729	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17870132	ATGACTGCATTAGGT[A/G]TATTTTGGTGGCACG	146691
rs554513924	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17967466	TGTATGTCATCCAAC[G/T]CCAAGCAGTTGTGGA	146691
rs554519105	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17846231	ACCATGGATCAGGAA[C/T]CTGTGCTGACCTAGG	146691
rs554557969	snp	C/T	0.00119737	0.0244387	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17846687	CTGTTTGCTGCTGGC[C/T]CTTGAGGCAGATGTG	146691
rs554558986	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17879034	TGGGCTGTCCAGAGG[C/T]GGGGAGGCCAGTTTG	146691
rs554567745	in-del	-/A			intron-variant	TOM1L2	GRCh38.p7	17:17914879	ATATCTTTTTTAGGT[-/A]AAAAAAAAATTTAAA	146691
rs554570794	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17924640	ATGGTGGTACATGCC[C/T]GTAGTCCCCAGCTAC	146691
rs554621463	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17879927	CTGCCTGTCAGCTCT[C/G]AGAGAGCTGAATGGG	146691
rs554658296	snp	A/C	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17880477	TCCTGTGCCTCAGAT[A/C]TGCCCCTTCACTCCC	146691
rs554671519	snp	C/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17941411	CTTGTTTAAAATCTT[C/G]GTTTTAAACAAGTTT	146691
rs554698449	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17871460	GGATCACTTGAGGTC[A/G]GGAGTTTGAGACCAG	146691
rs554713535	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17954028	AGTGCATTCAAATAG[C/T]CAGATAATTATTAAA	146691
rs554714232	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17895513	CATATGGAGTTTTAT[A/C]CAATTCTCACAACTA	146691
rs554760815	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17844965	AGGCTGGTGGGCCTT[A/G]AGAGTCCAGGTTTCC	146691
rs554795611	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17893230	CATCATTCTTCAGGG[A/T]CCAATGGAAATGTCA	146691
rs554825732	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17954578	TTGGCCTCCCAAAGT[A/G]CTGGGATTACAAGTG	146691
rs554831201	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17865413	TTTTGAGATGGAGTC[A/G]TCCCCCAGGCTGGAG	146691
rs554912685	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17920991	AAAGTTAACATTGGT[A/G]TAGTACTATTAACTG	146691
rs554920255	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17878390	AAGTTGTTTCCCGGT[C/T]TATTTCCTGCAAAAA	146691
rs554921051	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17949423	GGTCAGGAGAATAAA[C/T]GTTACAAAGTGCCCC	146691
rs554987047	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17887426	TCATATGTGAAAACG[A/T]ACAGATGGGAGACAT	146691
rs555019495	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17904623	GTTGTGCAGCAGGAA[C/G]GGGTAGGAGGGAAGG	146691
rs555019561	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17896873	CACAGGAAACAGGAG[A/G]ACTGAAAGTGACTAA	146691
rs555026688	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17859985	CAAAGGGTGAAGGGC[A/G]GGAAGTCACTCACAT	146691
rs555055219	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17897571	TCAAGACAGAAATAA[A/C]ACCTGAAGTCGTCTT	146691
rs555066137	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17911239	CGGCATCAGGATGCT[A/G]TGCTGCTCTTGCACT	146691
rs555094200	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17873608	AATACTCCCAGCACC[A/G]GCGGCCTGATGGAAG	146691
rs555103342	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17878492	ACAGGTCTCCACCCA[A/C]CCTCACCCCCATAAG	146691
rs555109350	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	TOM1L2, LOC100507131	GRCh38.p7	17:17858084	ATGCCAACTACTCCC[A/G]TGCCCTTGGAAAATC	146691
rs555119388	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17876793	ATTTGTATGCCTGCT[A/G]TGCTGCTGCCCGAAG	146691
rs555142678	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17933672	TTTAAAATGTTTAGC[C/T]TGGTGGAGCCATAAT	146691
rs555142774	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17929498	TAGCCAGGCGTGGTG[A/G]AATGTGCCTGTAATC	146691
rs555217185	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17949745	AGTCCAGTGGCCAGA[A/G]GGCAGAAGAGCACTC	146691
rs555230179	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17898279	TTGGTCTCAGTCTCA[A/G]AGCAGGCTGGTGACA	146691
rs555254628	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17895036	TGCATAGGGGAGGTG[C/T]CCAATAACTGATGAC	146691
rs555268331	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17938350	CCTCAGCAACCCAGA[A/G]AGCTCCTTCTACCTC	146691
rs555273702	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17902466	TGCTTGCATCCTGCA[A/T]GTGCCCTTCCAAGCT	146691
rs555274787	snp	C/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17947688	ACGTCTCATTTAATG[C/G]CCCGACACATACTTT	146691
rs555319717	snp	C/G	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17928580	GCCCCAGACGGCCCC[C/G]GCGTGAGCATGCACA	146691
rs555331238	snp	A/G			intron-variant, upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17971689	GCTGGGCTGGATAAA[A/G]ACACATGCAGTGGCA	146691
rs555341990	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17953141	CAAAAATTAGCCAGG[C/T]GTGGTGGTCACACCT	146691
rs555373687	snp	C/T	0.00318978	0.0398085	intron-variant	TOM1L2	GRCh38.p7	17:17956302	ACCAGATTAACTAGA[C/T]ACAGAGTGCTGATTG	146691
rs555405039	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17867028	TGGGACCAAGACCAG[C/T]CAGTCCCACCTGGGG	146691
rs555432358	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17949310	CTGAACATCTAGCAC[A/G]GCAGAGCATAGAGCA	146691
rs555440826	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17889490	CCTCAATCTGGCTGC[A/G]GCTCTGCTTCCACCA	146691
rs555486076	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17956683	CCAGCACAGCACTGG[C/T]GGGCCGGCACTGCTG	146691
rs555529660	snp	G/T	0.0310518	0.120672	intron-variant	TOM1L2	GRCh38.p7	17:17912976	ATCGCTCGCGGTTAG[G/T]AGCTGGAGACCGGCC	146691
rs555540711	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847424	GGGAGGGGAGAGAGT[C/T]TCTGGCTGCAGTTGT	146691
rs555545139	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17935754	TTAGGACATAAGGAA[C/T]GAGGTCACAAGTGAT	146691
rs555555427	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17925035	CTCCACTCTCTCTCT[C/T]TGTTTTTTGTTCCTG	146691
rs555579724	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17926421	ACTGGCACAAGGGGA[A/G]ATGCGGACATAAATG	146691
rs555589144	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17910670	TACCTCCTGGGTTCA[A/G]GCAATTCTCCTGTCT	146691
rs555683064	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17955887	AAGCTGCAGACCTTC[A/G]CGGTGAGTGTTACAG	146691
rs555697811	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17962905	GGCAGAGGTTGCAAT[A/G]AGCCGAGGTCGTGCC	146691
rs555754425	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17844279	GGCAGCGGGAAGGAG[G/T]GGGGCAGGAGCGTGA	146691
rs555760125	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17882346	AAGCCACCTGCTGCT[A/C]CGAGAGAGCAGCGTC	146691
rs555788036	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17959282	TAACCTCTGGGGTCC[A/G]CACCAGCTCCAGGTA	146691
rs555815890	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17876808	GTGCTGCTGCCCGAA[A/G]TCTAACCAAGATGTC	146691
rs555817431	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17928443	GGCAGGATAAAATAT[C/T]ATGTGCATACTAATC	146691
rs555841610	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17966078	GTGAGCTGAGATCGC[A/G]CCACTGCACTCCACC	146691
rs555853459	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17937429	GGTCCCATCAGGCTC[A/G]GATTAGGGGACTTTC	146691
rs555885926	snp	C/T	0.00358779	0.0422022	intron-variant	TOM1L2	GRCh38.p7	17:17868870	ATGCTCTAGATAACA[C/T]TGACATTTGCAAAGG	146691
rs555889816	snp	G/T			intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17858750	GCCACGCCCAGCTAA[G/T]TTTTGTATTTTTAGT	146691
rs555904865	snp	C/T	0.0023933	0.0345097	intron-variant	TOM1L2	GRCh38.p7	17:17922987	AGGCCAACCAGGGAC[C/T]GCAGGCATCACCAGG	146691
rs555913554	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17950732	TTCAATTGAGAGTGA[C/T]AGAAGCCTTTTAAAA	146691
rs555924873	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17883858	TATCCTTCTCAGAGA[C/T]GGGCAGTGGGGGCAG	146691
rs555944362	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17848733	GTAGGTGCTCTGGCA[A/G]CGGGGGCTCCAAGAT	146691
rs555975537	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17847924	GGTAGGGAGGGGTTC[A/G]TGAGCTGCAGTGTGG	146691
rs556025088	snp	C/T	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17895480	ATATGCCAGGCACTA[C/T]GAGAGATCCTTCCAT	146691
rs556051942	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17854886	TCCAAGCTGAAGGCT[G/T]GTCTGAGGGATCTGA	146691
rs556065610	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17896600	TGGGCTGGCAAGAGC[C/T]GCTTTAGGCCACCCT	146691
rs556068976	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17936370	CCCTGCCCCAACCTG[C/G]GCCAGGTTAGGTGGG	146691
rs556080792	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17849339	ACCAATAGCTGGAAA[A/C]CGCATGAGGCCTTGA	146691
rs556108795	snp	A/G			intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17858347	CTCACTGTGTTGCCC[A/G]GACTGGTCTCAAAAA	146691
rs556110685	snp	G/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17874976	AAAAAGGAAGAAAAG[G/T]CCATGCGTGGTGGCT	146691
rs556199792	snp	G/T	0	0	intron-variant	TOM1L2	GRCh38.p7	17:17884391	AAGTAGCCATTTCCA[G/T]GAAAACCCTGAACTG	146691
rs556200477	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17929302	TAGAGCTGCTTTGAG[C/T]AGCAGGCTTTGGGTG	146691
rs556210104	in-del	-/A	0.00318978	0.0398085	intron-variant	TOM1L2	GRCh38.p7	17:17917952	CAATGAGGCTGCCTT[-/A]AAAAAAAAACTGTCT	146691
rs556237347	snp	C/T	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17877520	GGCTGTTCAGTGTGG[C/T]TCTGACCCTTGGGAG	146691
rs556305396	snp	G/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17959396	TTTGCTGTCAGAAAT[G/T]TCATACATCACAGAC	146691
rs556314681	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17913970	TGTGAAGGGGAGAGA[C/T]TACTACCCCCTAGCC	146691
rs556336139	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17878386	AGACAAGTTGTTTCC[C/T]GGTCTATTTCCTGCA	146691
rs556336783	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17930245	GTGCTCCAGAAAGTG[A/G]GGTATAGAGAATTAC	146691
rs556376499	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17964188	CTGGTTTTAAAAGTC[A/G]CCTCTTTTAACCTCA	146691
rs556393221	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17885491	TGCCAAAAATGTCAG[C/T]ACATGTGTGCCCAAA	146691
rs556409695	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17939137	TGAAGTATCTTCCAT[C/G]TGAATTAAACCTTTG	146691
rs556425834	snp	A/G	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17851147	GCAGGTGAGGAAAGC[A/G]ATGAGGTGCAAATGA	146691
rs556466508	snp	G/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17864074	AGGTTTTGCTATGTT[G/T]CCCAGGCTGGTCTTG	146691
rs556488514	snp	A/G	0.0023933	0.0345097	intron-variant	TOM1L2	GRCh38.p7	17:17857189	CGATCTCCTGACCTC[A/G]TGATCTGCCTGCCTC	146691
rs556494235	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17915142	TATTATCTGAGTATC[A/G]GCGAAGTGTGGATTG	146691
rs556509116	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17907971	TTATGAAAATTAAAT[G/T]GGTTGATATACATGA	146691
rs556519848	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17916824	GGTTAGGAGTTTGAC[A/G]CCAGTCTGGTCAACA	146691
rs556608674	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17856604	CACAGCCTAGCATAG[C/T]ACACTATGGGCAGTT	146691
rs556719792	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17892559	AGCATGCCTCCTCAG[C/T]ATGCATGGCCACTGG	146691
rs556722106	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17946923	AGAAATGGAGTTTTA[C/T]CACGTTGGCCAGGCT	146691
rs556736442	snp	A/C/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17844997	GACAGAGCCGCACCC[A/C/G]CTTCCTGGACCAGGC	146691
rs556768440	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17915814	GGCATGAGCCACAAT[A/G]CTTGGCTCCATTTTT	146691
rs556775499	snp	C/T	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17923261	AAAAAATTAGCCAGG[C/T]GTGGTGGTGGGTGCC	146691
rs556775757	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17875089	TGGTGAAACCCCATC[C/T]CTACTAAAAATACAA	146691
rs556813639	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17968445	GCCAAGGAGGGTGGA[C/T]CACGAGGTCAGGAGT	146691
rs556813946	snp	A/C	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17923851	GTCTAAAAAAGAAAA[A/C]AAAAGGCCGGGCGCG	146691
rs556861133	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17926028	ATTTAAAAATTAGCA[A/G]GGCTCAGTGGCACGC	146691
rs556874525	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17924842	AGTATATTGATTCCA[C/T]TGAATATTATATAGC	146691
rs556881079	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17970255	ATTTTTAGTAGAGAC[A/G]GGGTTTCACCGTGTT	146691
rs556917518	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847302	TCTTTCTCCATGGGC[A/G]GGTGGAGGAAAGACA	146691
rs556922582	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17958415	TTTAAACCATCAAAT[A/C]TAGAGCTAAATAGTA	146691
rs556932463	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17868892	TTGCAAAGGGAAAAG[C/G]TTTTTTTCTTTTTTC	146691
rs556939865	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17904014	TATTATTATTATTTT[C/T]AAGATATGGGGTCTC	146691
rs556957115	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17864761	AGGTGATCCACCTGC[C/T]GCAGCCTCCCAAAGT	146691
rs556957229	snp	G/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17872604	CTCTCTGCTCTGCCA[G/T]GGACTGTTCCGGGCC	146691
rs556978036	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17969380	TGTTTTTAATCATTA[A/G]CTTTGTAGTTGTTAT	146691
rs556998662	snp	A/G	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17879554	TGCCGCTGTGTCCCC[A/G]GGTGGGATCCTCCAA	146691
rs557012941	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17932270	GAACTTATGAACATG[C/T]TTTTTATTTCATTAT	146691
rs557037351	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17942204	TGAAAACAGCAGACA[A/G]AAGTAAGGACCAGAC	146691
rs557037874	snp	A/C	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17972461	GGCCCCGCCCCCTTG[A/C]CGCGTCTCTATTGGG	146691
rs557081705	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17934627	TTCTCCTAAAAATAC[A/G]TATTTATTTTGTAAC	146691
rs557081943	in-del	-/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17878030	AGAGCAAATCCCCCC[-/T]GTCAGCAGGAATTCC	146691
rs557083372	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17865507	TCAGCCTCCTGAGTA[A/G]CTGGGACTACAGGTG	146691
rs557088524	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17956558	AGGGGTTTGCGCTCC[C/T]TGGGGAGGTTCGGGC	146691
rs557119490	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17931571	TTCTCTCCCCCTCCC[C/G]CGTACAAAATGAGCT	146691
rs557161741	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17881307	AAGCCCTGGGTCCTC[G/T]TGGCCAGGCTGGGTG	146691
rs557161834	snp	A/G	0.00318978	0.0398085	intron-variant, upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17972189	GCACCGGCGCCCGGC[A/G]GAGGCCCGCGGTCCT	146691
rs557170084	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17886481	CCCCACCAGCTGCGC[C/T]GGCTGCCTCCACCTG	146691
rs557196495	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17874144	GTATTTTAATAGAGA[C/T]GGGGTTTTACCATGT	146691
rs557197758	in-del	-/T			intron-variant	TOM1L2	GRCh38.p7	17:17915990	TGTCCCATTTATCTA[-/T]TTTTTTCTTTTGTTG	146691
rs557216107	in-del	-/CT	0.00279162	0.0372561	intron-variant	TOM1L2	GRCh38.p7	17:17906217	CACTGCAGCCTCGAC[-/CT]CCTGGGCTCAAGTGA	146691
rs557220054	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17948610	TGAGCTGGGACCATG[C/T]CACTGAACTCCAGCC	146691
rs557261684	snp	C/T	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17910567	TGATTATTACTATTA[C/T]TATTATTATTATTTT	146691
rs557276282	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17852592	TGAATTGAGCAGGGC[A/G]CGGTGGCTCATGCCT	146691
rs557288702	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17933755	CCAGAAAACCCACTC[A/G]TTTGTTACAACCACA	146691
rs557298714	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17903293	AATATTTATTAACAG[C/T]TAATCAAATGCATTG	146691
rs557316338	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17871716	TGAACTCTTGGTCCC[C/T]GCAAATTACCAGCTC	146691
rs557322848	in-del	-/A			intron-variant	TOM1L2	GRCh38.p7	17:17945217	GCCAGTAGGACCAAC[-/A]AGGTTAAAAATTAGG	146691
rs557359105	snp	A/C	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17897801	GAGCCTCAGTTTCAT[A/C]ATCTGTACGGGGGAG	146691
rs557402478	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17890180	AAGGTTGACCCAATG[A/C]AATGCTACTCCATGC	146691
rs557413695	snp	C/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17873679	CCCCAGCTGGGTGCT[C/G]GGGACGAAGCTGCAG	146691
rs557438837	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17889363	CTCTGAAAGGGAATC[A/G]GAAGGTGGGCTGGGG	146691
rs557441052	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17891233	TGGTGCTGGCCACTT[C/T]ACACCTTGGGCTGAT	146691
rs557460044	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17904690	GACACCAGAGAATGC[A/G]GCACCTGACCTTGAC	146691
rs557476200	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17847979	TCCTCCTGCCCTGGA[G/T]GGAAAGGCTCTGGAA	146691
rs557529521	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17922715	AGTGATATAAGACAC[A/G]AAACAGGGAACCTGG	146691
rs557615844	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17895101	TACACACGACGAAGG[C/G]GATGGCCTCTTATCC	146691
rs557626475	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17860164	GGCCAGGGTTGGCCA[C/T]GAGGAGGGGATGTCC	146691
rs557652552	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17895881	TACCATGTAACTTAA[C/T]CTAGGAGGCCAAAGC	146691
rs557660323	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17941543	ATCTTTTAGAATAGG[A/G]ATTCCAAGCCACGAG	146691
rs557668128	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17909521	CTAGATGATTCTACT[C/T]ACAATCAGGTACCTA	146691
rs557686991	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17956984	CGGGGCTGAGGAGGC[A/G]CCTGAGAGCGAGCAA	146691
rs557697692	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17888436	TTCAGACCAATAAAC[C/G]ATTGCTGATTTAAAC	146691
rs557723015	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17912362	GACGGGGTGGCTGCC[A/G]GGCGGAGAGGCTCCT	146691
rs557736633	snp	A/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17949865	TTTATTTTTATTTTT[A/T]AAATTTTATTTATTT	146691
rs557743608	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17854627	CTTCCCAGGTTCAGA[C/T]AATCCTTGTGCCTCA	146691
rs557746010	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17964551	TTCTCCTTTGCATTT[C/T]TTCTATATCTTTCAT	146691
rs557747247	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17913993	CCCTAGCCAGCTGGC[A/C]TCTCCCCTTCCTGGC	146691
rs557764269	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17905070	GCATGTTAGGAGGAC[A/G]TGAGGAAGGTAGCCA	146691
rs557784170	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17914944	GCAGACAGAAGACTG[C/T]TGCACAAATGTTTTG	146691
rs557799849	snp	G/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17950583	TGTATGCTCCCATTC[G/T]AATGAGAGTGAGTCT	146691
rs557857501	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17963275	GAGTGCTAAGTGCTG[A/G]AAGAGAACAAAGAGA	146691
rs557866607	in-del	-/G			intron-variant	TOM1L2	GRCh38.p7	17:17930877	CCACAGTCCTTCCTT[-/G]CTGATTAAAGGCAGA	146691
rs557894823	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17874631	AGGCTCTAACATTGT[A/G]ACCTCAGCTTGGAGG	146691
rs557899667	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17963610	AGCACTCAGCAAGGT[A/G]CCTGGCACATGGTGA	146691
rs557911573	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17927721	AGGCTGGGAATGCAG[C/T]GGCACAATCTTGGCT	146691
rs557919473	snp	A/G	0.00279162	0.0372561	intron-variant	TOM1L2	GRCh38.p7	17:17906215	CTCACTGCAGCCTCG[A/G]CCTCCTGGGCTCAAG	146691
rs557963542	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17919196	ACAGCACTCTCTCAC[A/G]CAGTGGCTGTTAGAG	146691
rs557985430	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17903945	GGGTGGGTGGGGTGC[A/C]CTACTGTCAGTCCAA	146691
rs558002116	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17919992	GGTCTTCCTGGTAAG[C/T]CTGGCCTTGGACCCT	146691
rs558002840	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17855762	TTCTGTAGCTCAGGT[A/G]TACTATTTCCAGAGA	146691
rs558007977	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17956480	GAGCTGCCTGCCAGT[C/T]CCTGGCAGTGCGCCT	146691
rs558025362	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	TOM1L2, DRC3	GRCh38.p7	17:17973407	TACTCAAGTTCTGTA[A/T]CCGTCTCTGTCAGTA	146691
rs558065803	snp	G/T	0.00636936	0.0560724	intron-variant	TOM1L2	GRCh38.p7	17:17853482	AATTTTCTTCTTTGG[G/T]GATAAATCTTGAGAG	146691
rs558070717	snp	G/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17921712	GGTGATCAGGTTACA[G/T]TTTCTGCTTAAAGCA	146691
rs558071129	snp	C/G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17928692	ATGGTTCCTCATGGA[C/G/T]CTGCCTTCCCTGATG	146691
rs558115931	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17938902	TAATTCTCACTTTCT[A/G]TACACTGGGGTGGGG	146691
rs558132916	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17897702	TCAGTTTTTACCCCA[C/T]GCAAAAGACCACTTT	146691
rs558147668	snp	C/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17966181	AGCTATTATTATTAC[C/G]ACCTGAGGTCACCCC	146691
rs558195539	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17950891	CCTAGGCCAGAGCCT[G/T]GGTGCAGAGGGAAAA	146691
rs558204022	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17899873	AATGTGTATGAGGAA[A/G]TTGAGGAGGGGAAAG	146691
rs558236060	snp	A/G	0.00318978	0.0398085	intron-variant	TOM1L2	GRCh38.p7	17:17968528	AAATTAGCCCGGCAC[A/G]GTGCCAGGCACCAGT	146691
rs558253107	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17930263	TATAGAGAATTACCA[A/G]CATACAAACTTTAGC	146691
rs558258423	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17967202	AGTAGTTTATGTCCA[A/G]CACCAGTCAGTCTAC	146691
rs558272408	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17867516	GGCAGTGCAGGGGGA[A/G]TTGGCTTTGAGCAAC	146691
rs558282678	snp	A/C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17862536	GTGTGTGTGTGTTTG[A/C/G]GGGGGTGGGGGAGGA	146691
rs558316291	snp	A/C	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17877613	GAGGCGTGCAGCCAA[A/C]CAGCCAGGACGGCTG	146691
rs558319633	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17863071	ACTGCTCAAGGAGGC[A/G]AAAGAGTCATAACAA	146691
rs558332983	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17916882	ACAAAAATTAGCCAG[A/G]CACAGTGGCTCACAC	146691
rs558355401	snp	C/T	3.29647e-05	0.00405971	intron-variant	TOM1L2	GRCh38.p7	17:17850874	ACCCCACAGATGAAA[C/T]AGAAAAGTCGAGTCT	146691
rs558429746	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17965684	CATACTTTCTCATTG[C/T]CTTAATGTCCCCATC	146691
rs558438787	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17849463	CCTCCTGGGAGCTGC[A/G]CCAGCCTCCTCCCGT	146691
rs558447703	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17876552	TTATAGGGAGCCACA[C/T]CTTAGATCAATGTGT	146691
rs558465449	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17899239	AGAAACCATATGAGA[C/G]ACACAGAAGAGAGCG	146691
rs558466449	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17844396	TCCCCAGGGGCTGGA[A/G]TGACAGCACAGGCCC	146691
rs558472492	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17938234	GGGATGTGCTGCCTA[A/T]GAGATAATGAGTTTT	146691
rs558499683	snp	C/T	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17926972	GGGCTAACAGACTTA[C/T]CACACACAGGTTGTG	146691
rs558568490	snp	C/G	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17900012	AGGACAGGAGTTTGA[C/G]ACCAGCCTGGCCAAC	146691
rs558595863	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17886602	TTCACAGCCCACTGT[C/T]GGAGGCTGGGGAAAA	146691
rs558602906	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17867830	TGTGGTTTTAAAAAC[A/G]ACTTGTGTGTTTTTT	146691
rs558604471	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17878318	ACTCCTCACTGGGGC[A/T]GGGCCAAGGGTACTT	146691
rs558632338	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17885185	TGTGCGGGAGCACCT[C/G]TGCCCTGAAAGCTTC	146691
rs558633006	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17887350	GAGGAAAAAATGGGG[C/T]GCAGGGGCGCCTCTG	146691
rs558670153	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17951835	TGTGGACCAACAACC[A/G]AATGCCTTTTCCCCT	146691
rs558687159	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17851535	GAACTGGAGGAGGTG[C/T]GTGCTCCGCTGGGCT	146691
rs558710568	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17906958	CAGCAGTGCAGGAAT[C/G]CAGGAGGGGCAACGT	146691
rs558712815	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17902412	CACAAATACAAGAAG[C/T]GCAGGCAGCACTTCA	146691
rs558745305	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17899902	AGGGTTGATGCTCTG[C/T]TAATCAGCTTAATTT	146691
rs558756828	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17856417	TGCCCAGGCTGACAG[C/T]AGAGCTGTGCAGAGG	146691
rs558765862	in-del	-/A	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17945797	ATAGAAAACTGGAAG[-/A]AAAAAAGAAGAAAAG	146691
rs558824786	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17864615	CTCCCGGGTTCAAGC[A/G]ATCCTCCTGCCTCAA	146691
rs558824817	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17857250	GAGCCACTGCACCCG[A/G]CCTGTGTATTCTTCA	146691
rs558846805	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17871606	AATCCGGGAGGCAGA[A/G]GCTACAGTGAGCAGA	146691
rs558854222	snp	A/C	0.000798403	0.0199641	intron-variant, downstream-variant-500B	TOM1L2, LOC100507131	GRCh38.p7	17:17857992	CCCAACCTCCACCCC[A/C]GCACGTCCCCCTTAC	146691
rs558862633	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17924519	TATTTAAAATCCTTA[A/G]CTGGGTGCAGTGGCT	146691
rs558881043	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17947319	ATGAGCCACCGTGCC[C/G]AGGCCAGTGAGCTTT	146691
rs558882111	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17851191	CCCGGCAGGGCCGGC[A/G]GTAAGGAAGGTGGCT	146691
rs558894168	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17893102	TAACACAGTGAGTGA[C/T]AACAAATACAACCCA	146691
rs558919083	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17845599	ACTGCCCGAGGTCGG[A/G]CCGCCCACCACCCGC	146691
rs558967859	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17939167	GCAAAGAGAGGCCAG[C/T]CCTCTCTAGTGTGAC	146691
rs559002754	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17947608	TTTCAGCCTCCAGAA[C/G]TATGAGAAAATAAGT	146691
rs559002854	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17940021	AACATGGTGAAACCT[C/G]ATCTCTACTAAAAAT	146691
rs559047630	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17911527	GGTGACAAAATAAAT[G/T]AGACTGAACTTTGCT	146691
rs559054329	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17940977	TTGTAAGATTTGTAC[C/T]ATTGGGATTCTCAAT	146691
rs559086742	snp	A/G	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17907260	CCTCCAAGCACTGCC[A/G]TTGGGCAAGTGGGGG	146691
rs559119828	snp	C/T	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17902843	GATACATCATATATA[C/T]TTACTCCTTTAATCC	146691
rs559125758	snp	C/T	0.00835141	0.0640778	intron-variant	TOM1L2	GRCh38.p7	17:17884323	TTCCCACACCAGATT[C/T]TAGGGGCCTCTGAAA	146691
rs559131061	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17874245	AGGCGTGAGCCACCA[C/T]GCCCAGCCATTACTT	146691
rs559155437	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17895208	TAAACCAACCCATAG[A/G]ATTACCTGGCCCTTC	146691
rs559179249	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17909045	AATTAGCCAGGTGTG[A/G]TGGTGGGCACCTGTC	146691
rs559179399	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17947982	ATTTCAGAAATACTT[C/T]TGATGGAGGAAAAGA	146691
rs559219985	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17846447	CACCAGTGAGGACAC[A/G]GGATGGGAATACATG	146691
rs559297077	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17901902	GTCTAAAACAGTCCC[A/G]GCTGGGTGCTCTGGC	146691
rs559329853	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17871933	AGGGGACACTACTAT[C/G]CAGTAAAGAGAAAAC	146691
rs559354235	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17963157	CTCCCTTCACCACCA[C/T]AGTTTACAGATTGGG	146691
rs559355682	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17972636	CCCCAAAGGGGAAGC[C/T]GCGCATTTTGATTCC	146691
rs559356780	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17876176	CCAGAAAGCCAAACT[C/G]AGGCTTTCTGCAGGT	146691
rs559417740	snp	C/T			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17844125	GGCTGCAAGCAAGTG[C/T]TCCTCCACACTGCTC	146691
rs559441933	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17866485	CTGAGGTAGAAGCTG[A/G]CAAGGCAACTATGCA	146691
rs559449215	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17860197	ACCAGGCAGTATCCT[A/G]GTAGGCCCCTGGCTG	146691
rs559474471	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17918727	GGCTCCAGCACCTGA[C/T]AGTACAGTTCACACA	146691
rs559490143	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17933044	TTAAACAGATGGGGG[G/T]TATTTTTCTCAGGGA	146691
rs559566472	snp	C/T			upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17972611	CGTGGCGGCACCTCC[C/T]CTGGCCCGCCCCCAA	146691
rs559605074	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17954219	AGGAGGGAGTGGGAA[C/T]GGCAAAGTAAGTAGA	146691
rs559688386	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17872776	CTCAGGACCCACCCC[C/T]TCCAGCAAACAGGCC	146691
rs559692461	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17962158	TATGAGGTTTCATAA[C/T]AAATATATGATTCCA	146691
rs559722575	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17919453	GGATTTCTGGGTTAC[A/T]GAGCCAGGAAGACCT	146691
rs559789198	snp	C/T	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17867237	GGGAGGGTGGCTTAA[C/T]CACCTTACCTTGGAG	146691
rs559809556	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17910892	CTTGATGGTTGGGGA[A/G]GTAGATCATTTGGCT	146691
rs559834965	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17876032	TTATGCTGATGAACG[C/G]CCACAGAAGAACATA	146691
rs559845622	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17961601	TTGAAGGGCCGGGCA[C/T]GGTGGCTTACACCTG	146691
rs559847772	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17911541	TGAGACTGAACTTTG[C/T]TTTCCTCTGGCCTGG	146691
rs559878523	in-del	-/G	0.00438332	0.0466095	intron-variant	TOM1L2	GRCh38.p7	17:17947209	TCAGTTTTATACGGT[-/G]GGGGGGGTCTCACTA	146691
rs559880179	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17853573	CTTCCCAAAAGCTGG[C/T]TCATGGGAACCCTTT	146691
rs559904140	in-del	-/A			intron-variant	TOM1L2	GRCh38.p7	17:17947462	AGAAGTGATTAAGTT[-/A]AAAATGGGGCCCTAA	146691
rs559950134	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	TOM1L2, DRC3	GRCh38.p7	17:17973492	CTAGCTGGGAAATAA[A/G]GGCATTAGGACTCCC	146691
rs560008730	snp	A/G	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17868245	TGGGGATGCCCCCAC[A/G]CTTACTGCAGAGGTT	146691
rs560030638	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17888595	GCCCAGCTACCAGGC[C/T]CTGACGTCTTCAAAG	146691
rs560032272	snp	C/T	0.00318978	0.0398085	intron-variant	TOM1L2	GRCh38.p7	17:17880223	TTTACATCTAAACAC[C/T]AGGATCCCTCTGAGA	146691
rs560045473	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17949481	AATACCACCCCACTC[C/T]GATGCTACAATCTGA	146691
rs560057896	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17927888	CAGGCCTCCCAAAGT[G/T]TTGGGATTACAGGCA	146691
rs560212445	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	TOM1L2, DRC3	GRCh38.p7	17:17974275	TCTACATCTTGCTAA[C/T]ACCCTGGTCATCTCT	146691
rs560213598	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17883689	CAGTGAGCCAAGATT[A/G]TGCCAGTGCACTCCA	146691
rs560225617	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17885861	ATCCGGGAGGCAGAG[C/T]TTGCAGTGAGCTGAG	146691
rs560240687	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17928814	TTTTTTTTCTTTAGA[A/G]CTATTCCCACCCACA	146691
rs560242996	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17937676	AGCAATGACACACAG[C/T]CCACATGCTACAGTC	146691
rs560243638	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17944257	TGAGTGGACAGGTGA[A/G]GACGGCAGGATGCTG	146691
rs560283005	snp	A/C	1.65853e-05	0.00287964	intron-variant	TOM1L2	GRCh38.p7	17:17898712	AAAGATACTTACAAT[A/C]CCACTTGAGGACACG	146691
rs560283630	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17923869	AAGGCCGGGCGCGGT[A/G]GCTGTCGCCTGTAAT	146691
rs560286976	snp	C/G	0.000399281	0.0141238	downstream-variant-500B	TOM1L2	GRCh38.p7	17:17843498	GCCAATTCAACAGAC[C/G]ACACAGGCATAATTT	146691
rs560299687	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17912606	GGCCGGGCAGAGACG[C/T]TCTTCACTTCCTAGA	146691
rs560321447	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17891625	CTGCAGACAGGCCTC[G/T]GGGTCAGAAAGCTCT	146691
rs560337039	snp	A/G	0.00517822	0.0506191	intron-variant	TOM1L2	GRCh38.p7	17:17913415	GGGCCATCCTGCCCC[A/G]GCTCTAAGCCCAGCC	146691
rs560375557	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17950075	GATGGGGTTTCACCA[C/T]GTTTCTCGATCTCCT	146691
rs560399875	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17890348	TGAGGTGGATACATA[A/T]GAAATTGCTAATATT	146691
rs560432115	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17861288	TGTGGCCTCATCTCA[C/T]GGGGTGAGGTGAAGA	146691
rs560481129	snp	C/T	0.000115751	0.00760672	intron-variant	TOM1L2	GRCh38.p7	17:17848911	GGTCCAAGCACTGCC[C/T]GCCCAGCCACCTCTG	146691
rs560481506	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17855850	AAGCCTTTGATCTCA[C/T]TCAATAGTACAAAAA	146691
rs560583324	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17959759	CTCTGAGATGAAAGA[A/C]TCAGTCTCTCTCCAT	146691
rs560584780	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17919676	ACGGTGTTGTTGCAA[A/G]TTCCCTATGGGCAGT	146691
rs560628798	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17944672	ACAATGATTTTTATT[C/T]AACATAGTATAAAAC	146691
rs560638344	snp	A/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17856797	GAGATGAGCTGACCC[A/T]CTCTCCATGCACCAG	146691
rs560646585	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17960814	CATAACCCAGTACCT[A/G]GTAAGGAGAGACATT	146691
rs560698837	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17965720	ATGGAGATAATCACA[A/G]TACCTTCCTCACAGC	146691
rs560718026	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17880013	CGTAGTGAAGGGCTC[C/T]GTGTCAGGAGTGCAC	146691
rs560725895	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17892302	CTTCCTGCATTCTCC[A/G]CTGCCTCTGCCTGGT	146691
rs560743690	snp	G/T	0.0023933	0.0345097	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17844680	CTCTGCAGCAGGCAG[G/T]CCAAAGGCCCATGGT	146691
rs560752497	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17930360	CTTGTGAAAGTGGTT[A/T]AAAAAAAGGGGGGTC	146691
rs560865295	snp	G/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17917305	CATCACTGCACTCCA[G/T]CCTGGGCGACAGAGC	146691
rs560868151	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17967896	ACAGGTGTGAGCCAC[C/T]GCACCTGTCCAGCTT	146691
rs560890438	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17897779	GGGTAAACCTCCAGA[C/T]CTCTCTGAGCCTCAG	146691
rs560891319	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17907644	AAGCAGATGGGCTGA[A/G]CCAACAGAGCCATTC	146691
rs560897879	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17863649	TGACCTCCCGGGCTA[A/C]GTGATCCTCCCACCT	146691
rs560925941	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17908445	GCAACAAAAGAAAAA[C/T]TTTGAACTACATCAA	146691
rs560929766	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17922980	GCCTGTGAGGCCAAC[C/T]AGGGACCGCAGGCAT	146691
rs560987141	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17879291	AGAAAGAAAATACAT[C/T]AAAGCACCTACAGTG	146691
rs561017368	snp	A/G	0.00398564	0.0444627	intron-variant	TOM1L2	GRCh38.p7	17:17849244	CAGGGGGCTGAGCCT[A/G]AGCACACACAGGGTC	146691
rs561060101	snp	C/G	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17872863	CCTTGGCTGGGGAGG[C/G]AGAAGGAAAAAAGTC	146691
rs561100173	snp	C/T	0.00557542	0.0525036	intron-variant	TOM1L2	GRCh38.p7	17:17874262	CCCAGCCATTACTTA[C/T]TTATTTATTTATTTA	146691
rs561108779	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17850800	TGACCCAGACAGGGG[C/T]GGAGCCCCTGCTGAT	146691
rs561204747	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17914319	CATTGTGTCCTCCCC[A/C]TTAACCTTCCTGGAA	146691
rs561246318	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17878712	TCATGCCAGGTTGCT[A/C]AATCAGTCTGGCTCC	146691
rs561249158	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17970535	GAGTGTGGCTGCCAT[A/G]CAAGAGCACCTGAAG	146691
rs561286861	snp	C/G	0.00159617	0.0282053	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17845641	TGGCAGGGCCTCAGA[C/G]ACAACCCAAGTCACA	146691
rs561346744	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17848512	CACCTCCACAAACTG[C/T]GTGTCTGAGCTGGGC	146691
rs561383928	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17896151	GTAGTGATCCATGGG[A/G]GCACTGAAATGAACC	146691
rs561389300	snp	C/T	0.0023933	0.0345097	intron-variant	TOM1L2	GRCh38.p7	17:17961639	AGCACTTTGGGAGGC[C/T]GAGGCGGGCGCATCA	146691
rs561395737	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17969684	TTCACAGGTCACAGA[C/T]GGGCCAGTTGTTTCA	146691
rs561396763	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17894545	CCCTGAATGGCCCAG[A/G]ACAGATCTTTCTGAG	146691
rs561415674	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17947014	ACAGGCGTACGCCAC[C/T]GTGCCAGCCTAAGTG	146691
rs561450524	snp	A/G			intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17860044	CTGATAATGGCAGGG[A/G]TGCAGCAGGACACAC	146691
rs561465524	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17900983	GAAAATAGGAAGAGC[A/G]CCTGAGGGCTGCAAT	146691
rs561479070	snp	G/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17948905	GACCCTGTGAGGGGT[G/T]GGGGGAAAGAGTTGG	146691
rs561483338	in-del	-/C	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17918582	GCAGGTCTTTGCAAG[-/C]CCTGAGAAAGTCACC	146691
rs561513058	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17964366	TTCCTTTCCTAATAT[A/C]CCAAGTAAATAAATA	146691
rs561518445	in-del	-/CAAT	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17865270	CTCTGTAGATATTGA[-/CAAT]CAATCAATCACAGAC	146691
rs561522708	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17909107	AATGGCGTAAACCCA[A/G]GAGGCGGAGCTTGCA	146691
rs561541222	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17959587	ATTCAGCTTTCAAAC[C/T]CCAAGCAACATCATT	146691
rs561591066	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17885768	TCTCTACTAAAAATA[C/T]AAAAAAATTAGCTGG	146691
rs561592295	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17888718	GCTGGGGCATGGGGA[G/T]GGGGGCTGGAGAGGC	146691
rs561597869	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17931244	AATCCTTCCTCTTCT[A/G]CAGATTTCCCCAATT	146691
rs561599370	snp	A/C	0.00318978	0.0398085	intron-variant	TOM1L2	GRCh38.p7	17:17902978	ATAAGCGAGTGGTGA[A/C]CTAGAATTGCTCCAG	146691
rs561632163	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17852930	GGGAGTCTTATCACC[C/T]AGACATGAAACCTAG	146691
rs561668806	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17846943	CCCAATTGTCCTTGG[A/C]CCTCTCCCTGCCCAG	146691
rs561682471	snp	G/T	0.0314385	0.121371	intron-variant	TOM1L2	GRCh38.p7	17:17865734	ATAAAACATGGCAGG[G/T]GACCTTTCTTTTTTT	146691
rs561760918	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17887590	AAGCAATCCTCCCAC[C/T]TTAGCCTCCAGAGTA	146691
rs561773232	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17961602	TGAAGGGCCGGGCAC[A/G]GTGGCTTACACCTGT	146691
rs561784035	snp	C/T	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17956588	CCGCATAGGAGCCCA[C/T]GGCAGGGAGGCTCAG	146691
rs561828210	snp	A/C	0.000798403	0.0199641	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17858828	CCTCGTGATCCACCC[A/C]CCTCAGCCTCTCAAA	146691
rs561829268	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17960965	AAACTTTTGTGCATT[A/G]AAGGACACTATAAAC	146691
rs561843980	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17956811	GAACTCGCGCTGGCC[C/G]GCAAGCGCCACGCGC	146691
rs561845826	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17949584	CTCTGGTCAGAGGAC[A/G]TATCTCAGTAAGTGT	146691
rs561856880	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17950273	ACAATTCTTGTGCCT[C/T]AGTCTTCCGAGTAGC	146691
rs561876770	snp	G/T	0.00159617	0.0282053	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17858321	TTTAAAATATTTATT[G/T]GAGATGAGGTCTCAC	146691
rs561888302	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17860227	GGGCTCTCTAATGCC[C/T]ACGCTGGGGCAGGTG	146691
rs561899958	snp	A/G	0.00557542	0.0525036	intron-variant	TOM1L2	GRCh38.p7	17:17962240	TAGTTGCCAGGGGCT[A/G]GGGGGAGGAGGGAAC	146691
rs561914093	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17934792	GTGTATGCAGGGCAC[A/G]GTGACAAGGCCACTG	146691
rs561914148	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17926661	TGAGCTCAGGAGTTC[A/G]AGACCAGCCAACATG	146691
rs561949890	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17927214	CTGCATTCTTCAATG[C/G]GGGTGGAGTCCAAAG	146691
rs561972064	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17955734	TCTCACTGACTTCAA[C/G]AATGAAGCCATAGAC	146691
rs562031745	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17948072	GAGATATATATTAGT[C/T]ATAATTGAGGAAACT	146691
rs562032552	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17853806	TCCTAAGAAGCCTTA[A/G]AGATTTGGGTGGAGA	146691
rs562059219	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17889223	AGAAAGCCCCCATAC[A/G]GGAAAGGAAGGAGTA	146691
rs562060317	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17956402	AAAGGTTCTCTAAGT[C/T]CTCACTAGACTCAGA	146691
rs562080722	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17852468	CTTCGGACCCAATGT[A/G]GGAAGCCCACAAGAG	146691
rs562115954	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17897226	TGAAAGCCACTCGTT[C/T]TGGGCATCACTCCTG	146691
rs562122399	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17870582	GATAAGACATGAAGG[A/G]TAAGTCTCTCCTTCT	146691
rs562123837	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17885380	GACTGTGGTTCAAGG[C/G]AAGAAGAGCCCATTG	146691
rs562127796	snp	C/G	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17912533	CTGGCAGAGGCGCTC[C/G]TCACATCCCAGACGG	146691
rs562149653	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17964818	TCCGATAGCCCACTC[C/T]TAAGCAGTGGCATTC	146691
rs562204587	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17861017	ATCAGAGATGTGGCT[C/T]GGGTCAGCATTGTCC	146691
rs562206016	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17972714	GACGAGTCAATCACG[A/C]AAATGGACGGAACAG	146691
rs562229638	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17869155	CTGCTTCTGCTGCTC[A/T]GTTCCCAGGAGGACA	146691
rs562248376	in-del	-/AGACATAA	0.00517822	0.0506191	intron-variant	TOM1L2	GRCh38.p7	17:17956381	TACAATCCCTTAGCT[-/AGACATAA]AGGTTCTCTAAGTCC	146691
rs562257519	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17869655	CCTGCCCCTCCTTCC[A/G]CAGAGGAAACAAGTA	146691
rs562307670	snp	G/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17918878	GGCAGGACATCTTCA[G/T]GTCAAGAAGGCCTGG	146691
rs562308770	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17873827	ACTGTCATGCTGCAG[C/T]GGCCTCCATGGCACG	146691
rs562344320	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17881620	AGGACCTCTTCCATC[C/T]GCCTGTCAAGCCCAC	146691
rs562345869	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17874312	GTCTTGCTCTGTCAC[C/T]CAGGCTGGAGTACGG	146691
rs562347568	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17866722	CAGGGGTGCCTGCTA[C/G]CTCTGCCCTAGTATC	146691
rs562382056	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17867381	CAGCAGGAGGAAGGC[A/G]GACGCATGGCCCTGG	146691
rs562398646	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17926589	ATATTTGGGCCTGGT[A/G]TGATGGATTACACCT	146691
rs562431286	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17928863	CATTCCTCAGTATCA[C/G]AGAACAATGCTTCCA	146691
rs562432660	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17965902	AAGGTGGGTGGATCA[C/T]CTGAGGTCAGGAGTT	146691
rs562465339	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17862026	CCGACTCCTTTAGCT[A/G]TATCTGTTTTACAAT	146691
rs562467551	snp	A/G	0.00438332	0.0466095	intron-variant	TOM1L2	GRCh38.p7	17:17921898	ACCACCAGCACTCTC[A/G]GAGAAGAGAGGAGGT	146691
rs562482854	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	TOM1L2	GRCh38.p7	17:17843078	CAGTTCTCAAATTCA[A/G]TGCCCAGCACAGGCT	146691
rs562488071	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17913634	GAAAAGAAAGAAGCA[C/T]TCTTTTTGGGTTGGT	146691
rs562496351	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17943478	ACACTTGGGTATGGA[A/G]AGAATGTGGATGATC	146691
rs562533596	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17892034	AGGGAACGAAGAATG[A/T]GGCAGACAAAAGAAA	146691
rs562533745	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17900014	GACAGGAGTTTGAGA[C/G]CAGCCTGGCCAACAT	146691
rs562570468	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17892517	AGCTCAGAGCCCTTC[A/G]ATGTCTTCCCACTGC	146691
rs562577842	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17890458	CTCAAGAAAAGTCAA[A/G]TGCTAGATGCTCATA	146691
rs562615503	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17882542	GACCACAATCCATCA[C/T]GACTTCCTCAGCATC	146691
rs562626631	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17966399	ACATTTAATGTTTGA[A/T]GAAAGATAAAGAAAA	146691
rs562631672	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17936055	CCTTTACGGTTTCCC[A/G]CTGCTGTTAGGACAA	146691
rs562637011	snp	C/T	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17962829	AGCTGGGCGTGGTGG[C/T]GCGTGCCTGTAGTCC	146691
rs562661143	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17897971	CACTCTGTTGCCCAA[A/G]CTGGAGTGCAGTGGT	146691
rs562670225	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17930428	ACAAGGAGGACTGCA[C/G]AGACCCTCACGGTAG	146691
rs562777897	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17884275	AGTGACATCAAGCCC[C/T]GAGGTGCTATGGTGC	146691
rs562794425	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17899460	GTCCAAAAGTTGGAG[C/T]GGAGCTGTTTGGAAG	146691
rs562796815	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17928269	ATTCTGCAAAGATGC[A/G]TAATTGAGAAAAACA	146691
rs562813796	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17883271	TTTTTTGGTCTTTAC[A/G]AGTAGACTAATATAA	146691
rs562837702	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17850262	GTAAAGAACAGAGGG[A/C]GGGGCCAGCAGTTAT	146691
rs562852672	snp	A/T	0.0240643	0.107019	intron-variant	TOM1L2	GRCh38.p7	17:17945294	CACACACACACACTC[A/T]CTCTCTCTCTCTCTC	146691
rs562861764	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17920053	CAAAGAAGACCCTGG[A/C]CTCCACAATAGACGG	146691
rs562889117	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17953376	TCTGGTCCTTGAGCA[C/T]GAATTAATCAGGAAG	146691
rs562899133	snp	G/T	0.00398564	0.0444627	intron-variant	TOM1L2	GRCh38.p7	17:17855236	TGCCTGCCCAAGGGG[G/T]AGAGGCATGTCTGTC	146691
rs562919399	in-del	-/A	0.00438332	0.0466095	intron-variant	TOM1L2	GRCh38.p7	17:17939376	ATTCTATTCAGTCTT[-/A]AAAAAATATATGACA	146691
rs562921400	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17905636	CTCGAACTCCTAGGC[A/G]TAAGCAATCTTCCTG	146691
rs562926513	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17917505	GGTCTTGCTATGTTG[A/C]CCAGTCTGGACTCAA	146691
rs563006130	in-del	-/AGGCTGACCCAGCTGAG	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17887976	AGGAGGGGTGCTGGA[-/AGGCTGACCCAGCTGAG]AATACTCCCTAGAGA	146691
rs563018969	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17954136	GTTTCAAAGGGTATA[C/T]TGGTCTAAACCATGA	146691
rs563051881	snp	A/C/G	8.2386e-05	0.00641774	missense, upstream-variant-2KB, intron-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17862764	AAGGAGTTTCCTCTC[A/C/G]TCTGGGCAAACATGT	146691
rs563100661	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17961535	AGCTATGATCATGCC[A/G]CTGTACTCTAGCCTG	146691
rs563106550	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17870238	GTTGCCCCTGGAGCC[C/T]TCTCTACCCTTAGAA	146691
rs563110421	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17906623	ACTGCTGTGTCCTCA[A/G]TATTTACAATAGGGC	146691
rs563115124	in-del	-/A	0.00318978	0.0398085	intron-variant	TOM1L2	GRCh38.p7	17:17949792	AGATCACCAGTGGGC[-/A]AAGTTTAGGTGGGCC	146691
rs563143963	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17924140	AGACTCTGTCTCAAA[C/T]AAAAACAAAAACAAA	146691
rs563155470	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17908921	GGCGCGGTGGCTCAC[A/G]TCTGTAATCCCAGCA	146691
rs563187868	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17855990	ACAAACTGCAGTCAG[G/T]CAGGCAAGACACCAG	146691
rs563203458	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17849557	AATTAAAGTGCATCA[C/G]ACTTGATTTTGTTTG	146691
rs563234759	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	TOM1L2, LOC100507131	GRCh38.p7	17:17858146	GCTTCTCTCAATTAC[A/G]GCTATCAGGGTTGGG	146691
rs563301923	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17931136	TCCCATCCCCACAAA[A/G]AACTACACATTCAAC	146691
rs563327286	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17893934	ATCAGCTTTCTGACA[C/T]GTCTCCTCCAGAGCC	146691
rs563344662	snp	A/G	0.00358779	0.0422022	intron-variant	TOM1L2	GRCh38.p7	17:17932420	CAGGTATGAGTTACC[A/G]TGCCCAGCCCTCTTT	146691
rs563353415	snp	A/G			intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17860495	GAAGGAGCATCCCGT[A/G]GAAACCAGCACTGCT	146691
rs563386963	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17878480	GTCAGGCCTGGAACA[A/G]GTCTCCACCCACCCT	146691
rs563390919	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17936324	CCTTCTTCCAGGAAG[C/T]TTTCCCCAACCCTGT	146691
rs563418692	snp	C/G			utr-variant-5-prime, upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17972421	CCCCCTCCCCACTCT[C/G]TGGAACGCCGAGCTT	146691
rs563428810	snp	G/T	0.00597247	0.0543191	intron-variant	TOM1L2	GRCh38.p7	17:17865781	ACAGTGTCTTGCTCT[G/T]TCGCCCAGGCTGGAG	146691
rs563559027	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17871227	CACAAAAAATTAGCC[A/G]GGCGTTGGTGGCGGG	146691
rs563560874	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17863840	AAGTGTGAGCCACCA[C/T]CCCTGGTGGACACTA	146691
rs563589845	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17968756	CTTGCCACCACTCCC[C/T]ACAGCCACCTCTGCT	146691
rs563594083	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17910119	GACAGAAAAATTATA[C/T]ATAGGTCAATGGACT	146691
rs563600260	snp	A/C	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17960914	ATGACACGGAAGGTA[A/C]AAGCAACAAAAGAAA	146691
rs563633473	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17962975	CAAAAAAAAAAAAAA[C/T]GTAAATTTTGTTATA	146691
rs563643215	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17916136	TGGAGTGCAGTGGCG[C/T]GATCTCAGCTCACTG	146691
rs563661070	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17897984	AAGCTGGAGTGCAGT[A/G]GTGCGATCTCAGCTC	146691
rs563734082	snp	A/C	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17888919	GGCATGAGGTGAAAA[A/C]ATAGGGGTGAAGCTG	146691
rs563761765	snp	C/T			intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17859326	GTGATCCGCCCGCCT[C/T]GGCCTCCCAAAGTGC	146691
rs563793725	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17962413	GCAACCTCCTCCTCT[A/G]GCAATTCTCCTGCTT	146691
rs563816504	snp	C/T	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17940855	TCTCATAAATTGTTT[C/T]CTTGGCTGGATCCCA	146691
rs563818412	in-del	-/T			intron-variant	TOM1L2	GRCh38.p7	17:17969058	AGGGACCAGCTCTCC[-/T]TTTTTTTTTTTTTTT	146691
rs563823299	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17858854	TCAAAGTGCTGGGAT[C/T]ACAGGCGTGAGCCAT	146691
rs563838196	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17880099	CCTCTCAGGGCTTCC[A/G]TTCCTGCTCTTTAAA	146691
rs563855793	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17947511	GAGGAATGACCATGT[A/G]AGGACACAGCAAGAC	146691
rs563863724	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17894637	GATTAGCAAGAATAC[A/G]TTTAAAGCATAGGCC	146691
rs563875503	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17856189	GGCACAAGGGCATGT[A/G]GGCTGGATCTTCCCA	146691
rs563879896	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17940150	GTGAGCTGAGATCAC[A/G]CCTCTGCATTCCAGG	146691
rs563994421	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17896268	GGTGTTGGGGTCAAG[A/G]CAGATGGCAAGAAGT	146691
rs563997354	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17881787	GCTCTCACCGTACTC[C/T]CTGCTCAGAGCTAGC	146691
rs564019089	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17925451	TTACTGTTACAAAAA[C/G]AAGGAAAGAGGATAT	146691
rs564039660	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17936581	AGGAAAAAAAGAAAA[G/T]AAATAATCTAAATGT	146691
rs564074909	snp	A/C	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17927270	ACACTGTACCAAGTC[A/C]AGCTGGTATGTGGAT	146691
rs564079321	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847495	ACTAGTGGGAGGCCT[A/G]GGAGCAGACACGGTG	146691
rs564091654	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17955821	GATGTTCAGCTGTGT[C/T]CTGAGTTTCTTCCTC	146691
rs564105924	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17910765	AGTAGAGATGGGTTT[C/T]GGCACGTTGGCCAGA	146691
rs564140466	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17881001	TGCCATCTTCCACTA[C/T]TGCAGCTGTAGCAGC	146691
rs564144962	snp	C/T	0.00318978	0.0398085	intron-variant	TOM1L2	GRCh38.p7	17:17903537	AGAATGGCATGAACC[C/T]GGGAGGCGGAGCTTG	146691
rs564160668	in-del	-/A	0.00478085	0.0486577	intron-variant	TOM1L2	GRCh38.p7	17:17929638	CTCCATCTCAAAAAC[-/A]AAAAAAAAGAATGTC	146691
rs564183477	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17964711	TTTAACTACGATCCT[G/T]CCACTGCATTCCAGC	146691
rs564218803	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17950803	AAATCTGTGACAGCA[C/T]AGGTGGCTCATAGAT	146691
rs564237739	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17943573	AGGGGAGCCCGAAGG[C/T]TGAGCTGCCTCCAGA	146691
rs564249406	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17902737	CCCAAATGAAAGTGA[C/T]GACAAAAGTCATGGG	146691
rs564257514	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847006	GCTGCTGAGCCAGCT[C/T]GGGTGTGAAGCCTGG	146691
rs564283267	in-del	-/TC	0.157599	0.232298	intron-variant	TOM1L2	GRCh38.p7	17:17969861	GAATAGGAATCTTTC[-/TC]TCTCTCTCTCTCTCT	146691
rs564318634	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17904871	CAGGAAGCATTGATA[C/T]CCACCTTTCCCTCTG	146691
rs564353743	snp	A/G	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17958359	TGCCAGAAAAAGTAG[A/G]TAAAACAGAAGACCA	146691
rs564355537	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17898147	GCCAGGCTGGTCTTG[A/G]ACTCCTGACCTTGAG	146691
rs564362509	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17911776	GAACAAAGGTCTCTG[C/G]TTTTCCTAGGCAGAG	146691
rs564362612	snp	C/T	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17920703	GCAGTGGTGCGATCT[C/T]GGCTCACTGAAACCT	146691
rs564369328	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17904930	CCACAGCCCTTGCCA[C/G]TCCTGCCAGGTGAGC	146691
rs564387265	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17893888	GAGGAGCGCAGCTGA[A/G]TTTCCACCATCCCCT	146691
rs564398223	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17912597	ACGATGGGCGGCCGG[A/G]CAGAGACGCTCTTCA	146691
rs564409580	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17949426	CAGGAGAATAAATGT[G/T]ACAAAGTGCCCCTTC	146691
rs564449601	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17926420	GACTGGCACAAGGGG[A/T]GATGCGGACATAAAT	146691
rs564469564	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17957437	CTGCAGTGTGTTGGA[A/G]GAGAGGATTAACTGG	146691
rs564506825	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17914656	GGTGCCATCTGAGGA[A/C]TGACTTTGGTTAAGA	146691
rs564522063	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17905342	CTCTGCTCCCCAGCC[A/T]GCTCCACCTCAGGAA	146691
rs564541318	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17890608	ACCTAGAATCACAGG[C/T]AACAATGCGTGTGAC	146691
rs564566335	in-del	-/A	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17957934	CTCTACTAAAAATAC[-/A]AAAAAATTAGCCGGG	146691
rs564567519	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17966522	ATGCTACTTCCCACC[C/T]CAAACCTACTGAAAC	146691
rs564599401	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17854986	TAGCAGAGGAATGCC[C/T]TCCAATAGAGACTGC	146691
rs564617202	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17965005	TCAATGCTCCATCAA[C/T]CTGCCTTGGCACCTT	146691
rs564620829	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17862922	TGAAGGGCCCCCAAG[C/T]TAGGACGCCAGCCAG	146691
rs564631069	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17967751	TAGCTGGGATTATAC[A/G]CGCGTGCCACCATGC	146691
rs564637967	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17848766	TGGGGGCTGGCTCCT[C/G]TGCAGCCTGCACAGA	146691
rs564658164	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17863529	TGGTAATACCTCAAA[C/T]GCCAGGTAAAGGAGT	146691
rs564686510	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17893234	ATTCTTCAGGGTCCA[A/G]TGGAAATGTCATCTC	146691
rs564693493	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17865412	TTTTTGAGATGGAGT[C/T]GTCCCCCAGGCTGGA	146691
rs564699635	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	TOM1L2, DRC3	GRCh38.p7	17:17973389	TTTGGATGTGAATAC[A/G]GCTACTCAAGTTCTG	146691
rs564709273	snp	A/G	0.00159617	0.0282053	downstream-variant-500B	TOM1L2	GRCh38.p7	17:17843415	AAGGGTGGACTGAGG[A/G]TCCCCATGGCCACCC	146691
rs564715572	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17867463	AGTCATCGAAGGACT[A/G]CTAGGAGGGTGGAGT	146691
rs564752390	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17868123	TAAACCCAAGCCCAT[G/T]TACCATGGAGAAACT	146691
rs564756606	snp	A/G	0.000798403	0.0199641	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17860352	CCTGTGGAAAGGCAC[A/G]GCACTGAGGACCCAA	146691
rs564769064	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17855565	GCCCTAGCCCATTGA[C/G]AAGTCTCATTTCTCT	146691
rs564784802	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17906788	CAGCTGCTCTCCTTG[C/G]CACTCCTGAAAATGG	146691
rs564822254	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17958638	AAGAGTCATAAAACT[C/G]AGTCACTGTGGGACC	146691
rs564829065	snp	A/G			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847467	AGAAAAGAAGTGGCT[A/G]AAGCTGGTCCTGACT	146691
rs564834203	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17951550	GAGTAGCAGACAGGT[A/G]AGGCAAATAAATAAA	146691
rs564898243	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17854120	TTCTTGTGGCCAGAC[A/C]CAAAACCTTAGCTAT	146691
rs564941500	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17869753	TAAAAAATATTAAAA[C/T]GTGATTCTTTCCAGA	146691
rs564981096	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17885709	GCGGACGGATCACGA[A/G]GTCAGGAGATCAAGA	146691
rs565002938	snp	A/G	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17876237	AGTGTCTTGAATTTC[A/G]GGCCCAGACCTAAGG	146691
rs565019646	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17914058	GCTGCTTCCATCAGG[A/G]TAAGTCTCCTCTTGA	146691
rs565041197	snp	C/T	8.32882e-05	0.00645269	intron-variant	TOM1L2	GRCh38.p7	17:17869330	AAAAAAAAAGAAATC[C/T]GGCTCCCACCTCTCG	146691
rs565066495	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17891553	GTGCAGTTCACACCC[A/C]TTGTGATAACTGTGC	146691
rs565098824	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17856708	CTGCATTCTCTCCAG[C/T]TCAGGCTCCATCACA	146691
rs565177115	snp	A/G			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17844244	GAGATGCGTGTCTGC[A/G]GGGGCCCAGGGTGGG	146691
rs565191915	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17876958	GGAAGGTCTCTCCCA[A/G]CTCAGAGAGTGGAGG	146691
rs565193064	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17943568	TGGAAAGGGGAGCCC[A/G]AAGGCTGAGCTGCCT	146691
rs565207531	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17892612	CATCTCCTGCCTGCT[C/G]CCCCACCCCAAGCCC	146691
rs565229128	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17922258	AGGAATTTGAAGAGA[A/G]AGGAACATCATAGGC	146691
rs565241802	snp	A/G	4.94173e-05	0.00497053	synonymous-codon, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17884727	ATATATGTGCACAAC[A/G]CCGGTGAGATCAGGA	146691
rs565243673	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17893433	GAGCAGCAGAGGGAT[A/G]GCACCCAGAAAGCTT	146691
rs565294559	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17939717	AAAGTAAATTTGAAG[A/G]TAAAATTGACACATT	146691
rs565328934	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17910563	TCAGTGATTATTACT[A/G]TTATTATTATTATTA	146691
rs565331243	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17899601	TTATTCTAACTCAGG[A/T]TTCAACAAAGCTGTG	146691
rs565360425	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17876016	GGCCTCTGTTATTAT[C/T]TTATGCTGATGAACG	146691
rs565395752	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17968844	GTCCCTAGGCCCAAT[G/T]ATATTGTTTTCTGCA	146691
rs565408199	in-del	-/TGTTT			intron-variant	TOM1L2	GRCh38.p7	17:17934565	AATTATGTCTTACTG[-/TGTTT]TGTTTTGTTTTGTTT	146691
rs565408799	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17900705	ACAAGGCTCCATGGG[G/T]ACTGGGCCCAAGGCC	146691
rs565418791	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17953124	TCTCTACAAAAAAAA[C/T]ACAAAAATTAGCCAG	146691
rs565475350	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17850710	GGCCGGGAGGCCACT[C/G]CAGCACCCACAGCTA	146691
rs565491796	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17942404	TTAATCCTGGCTTTA[A/C]CCCTCAATCATATCA	146691
rs565501237	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17845370	CGCTGGAGCTGGAGC[A/G]GGGCAGTTCTGGGAG	146691
rs565506686	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17900043	ATGGTGAAACCCCGT[C/T]TTTACTGAAATATAC	146691
rs565536500	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17894105	CTAGTGTTTTAATGG[C/G]ATCAAAATGACTGAG	146691
rs565572908	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17945452	ACATCAAAACAAACA[C/T]GGATTTCAATGTGCA	146691
rs565611997	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17938616	CTCCAGATTCCACTT[C/T]TACCCACATACTCAT	146691
rs565619229	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17945922	CACCCAGGCTGGAGT[A/G]CAGTGGCACAATCAT	146691
rs565635115	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17854670	GCTGGGATTACAGGC[A/G]TGAGCCACCACACCT	146691
rs565655338	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17938920	CACTGGGGTGGGGCC[A/G]CCCAGAGAAGCTAAA	146691
rs565657301	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17946763	AGAGTCTCACTCTAT[C/T]GCCCAGGCTGGAGCG	146691
rs565671786	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17931927	AACCCGAGGTGGCCA[C/T]CTTACCCAAAGATCT	146691
rs565686896	snp	G/T	0.00279162	0.0372561	intron-variant	TOM1L2	GRCh38.p7	17:17851558	GCTGGGCTGGGTGTG[G/T]CCTGGTAGACAGAGG	146691
rs565688809	snp	A/G	0.00953873	0.0683987	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17858979	GCTGGGATTACAGGC[A/G]TGAGCCACTGCGCCC	146691
rs565708165	snp	A/C	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17886138	TCCCTCACTCCAGCA[A/C]TGTGGTACAACCAAT	146691
rs565714871	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17941440	TTAAACTTCATGGCA[G/T]CAGGAAAACAAAACA	146691
rs565772091	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17871443	GGGAGGCCGAGGCAG[A/G]CGGATCACTTGAGGT	146691
rs565785104	snp	A/C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17879476	CCTGTCCGTAGGCAA[A/C/T]GTGAGGCTGCATGTG	146691
rs565802504	snp	A/C	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17924596	CAACATAAACCTTGC[A/C]TCTACAAAAAATACA	146691
rs565828957	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17953534	GAGGCAGATCCCAAA[C/T]AGGGACCACCATGGG	146691
rs565832479	snp	A/G	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17857049	AATCTCTGCCTCCCA[A/G]GTTCAAGCGATTCTC	146691
rs565890230	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17900440	GGCAAGAGAATTGCT[A/T]GAACCTGAGATGTGA	146691
rs565920678	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17870519	TAAAGCAGAGGGAAA[C/T]GCTGTTCCCACCTAC	146691
rs565938371	snp	A/C			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17846392	CTGGCTGGACCAGGG[A/C]CTGGGATGACCCGAG	146691
rs565964374	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17857511	AAGGAAGGAAAGGAC[C/G]CTCTCCTCATCCCTG	146691
rs565977322	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17970047	TTTGGTTTTTTGTTG[C/T]TGTTGTTGTTGTTTG	146691
rs565990770	snp	C/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17844947	TTTCTAACACTCACG[C/G]AGAGGCTGGTGGGCC	146691
rs566051511	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17962514	AGACAGGGTTTCACC[A/G]TGTTGCGCAGGCTGG	146691
rs566132892	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17911208	CTACCCCAGGCGAGA[C/G]AAAATGCCATGGCAA	146691
rs566173566	snp	A/G	0.00438332	0.0466095	intron-variant	TOM1L2	GRCh38.p7	17:17874404	GCCTCCCAAGTAGCT[A/G]GGATTACAGGCACCC	146691
rs566186276	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17872286	ATCACATAGATCACG[A/T]GAAGGATTCCAACAG	146691
rs566197465	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17941377	TGACTATGGACGACT[C/T]CCTTATATGCTTGGC	146691
rs566223129	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17865286	AATCAATCAATCACA[G/T]ACTTTTCTAAGCCCT	146691
rs566275703	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17887820	TCTCTCACCCGTGTA[C/T]AGAGAAGGCAGTCAG	146691
rs566278444	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17912092	ATCCGATTTCTCAAT[A/C]TTTTCCCCACCTTTC	146691
rs566301508	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17896525	TGCCCTGGACAGAGA[C/T]GCATGTGCCACAGAG	146691
rs566310447	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17919052	GGAGAAATGTGCATT[A/G]TAATGGAGTCTAGAA	146691
rs566311977	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17936969	AAGCTGCCTCATACC[A/T]TGAGGGCTCAGAGTT	146691
rs566319510	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17888292	AAAAAGGAAAGAGAT[C/G]AATTCAGATCTCCTT	146691
rs566357488	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17889104	AGCCGACTGAGCCCT[C/T]GCACATGTTGGTAAA	146691
rs566364892	snp	C/T	0.00318978	0.0398085	intron-variant	TOM1L2	GRCh38.p7	17:17970685	TTATAAAAGATACTA[C/T]GCCAGAAAGTAAAGA	146691
rs566373428	snp	C/G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17970174	ATTCTCCTGCCTCAG[C/G/T]CTCCCGAGTAGCTGG	146691
rs566379607	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17865815	AATGATGCGATATCG[A/G]CTCACTGCAACCTCC	146691
rs566382742	snp	C/G	0.21303	0.247251	intron-variant	TOM1L2	GRCh38.p7	17:17867022	AATCCCTGGGACCAA[C/G]ACCAGCCAGTCCCAC	146691
rs566383758	snp	G/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17954515	ACGGGGTTTCGCCAT[G/T]TTGGCCAGGCTAGTC	146691
rs566423895	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17909483	TTGTGCTAAGTGAAA[A/T]AAGCCTTTCACCAAG	146691
rs566443280	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17954770	AACTTACAGCCTCAA[A/G]CAATGGTCCAGGCAT	146691
rs566462690	snp	C/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17972175	CCGCTCGTGAAGTGG[C/T]ACCGGCGCCCGGCGG	146691
rs566481974	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17936181	CCCCCAGGCGTGTGC[A/C]CTTCAGCAGCTCTGG	146691
rs566506673	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	TOM1L2, DRC3	GRCh38.p7	17:17972849	TGGTCACGTGACTTG[C/T]CAACTTTCACCCAGG	146691
rs566521951	snp	A/G	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17963470	GGAGAGGACCGCTCC[A/G]CCTACTTGAGCCAGG	146691
rs566538100	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17885699	AGAGGCCGAGGCGGA[C/T]GGATCACGAGGTCAG	146691
rs566543426	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17867587	AAGAGTAGTTATGAG[G/T]TGTGTGTTGGGGTGG	146691
rs566554658	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17859865	CAACCTGGGCGCCAG[A/G]GCGAGACTCCATCTC	146691
rs566556264	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17922742	CTGGAACATAGTGAG[A/G]GCGCAATAAATATGA	146691
rs566569196	in-del	-/CA	0.00279162	0.0372561	intron-variant	TOM1L2	GRCh38.p7	17:17906202	GGCATGCTCATGGCT[-/CA]CTGCAGCCTCGACCT	146691
rs566619752	snp	G/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17928538	CCCTCCCTTTAACAC[G/T]CAGCTCGTTGCCTCC	146691
rs566623679	snp	A/G	0.00159617	0.0282053	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847055	GAGAGAGGGTCAAGA[A/G]GGTGAGAGACCCCCA	146691
rs566655513	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17873961	ATTTACTTACTTATT[A/T]TTTTTTTTTTTTAGA	146691
rs566681667	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17926924	GAAGAAGAGCCCCAA[C/T]ACAAGCATGTATTCC	146691
rs566710524	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17904586	ACCCCTGAAGGCTTG[C/T]TAGCAAGGGAGCAAC	146691
rs566747596	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17904945	GTCCTGCCAGGTGAG[C/T]GTTCAAGGGCAGGCT	146691
rs566774253	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17918455	CTATATATATTTTTA[C/T]AAAACACAGTCATAC	146691
rs566835671	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17873986	TTTAGATGGGAGTCT[C/T]GCTCTGTCGCCCAGC	146691
rs566853465	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17868827	AAGCAGCAGCATTCC[A/G]GCACTTACACCCGCC	146691
rs566875974	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17849323	GGAAGACGCTGTTGA[C/T]ACCAATAGCTGGAAA	146691
rs566878013	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17856267	TGTGGGCCAGAGGCC[A/C]GCCTGTCCCTGAAGA	146691
rs566908494	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17911238	ACGGCATCAGGATGC[C/T]ATGCTGCTCTTGCAC	146691
rs566974683	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17876411	CTGCCAAATGCCACA[G/T]TTGTTCCATGTGGAG	146691
rs566987554	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17949712	AGAAGGCTGGTGGTG[C/T]GTCCCGAAAAGGTGC	146691
rs567004410	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17889894	AGCATCCTGATACCA[C/T]GATGGTGCAGAGAAG	146691
rs567005190	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17955490	ATTACAGGCACACGC[C/T]ACCAAGCCCAGATAA	146691
rs567014406	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17849941	TGTTTGGAAAGCTGA[C/T]CTTCTGGGGAGGAGG	146691
rs567021981	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17854087	GTTAAGCTTATATAA[C/T]GTAAGCTTAAATTGA	146691
rs567043265	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17847884	CTCCTCTAGGGCAGG[C/T]ATGAAGCCCACCTAG	146691
rs567183202	snp	G/T	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17958021	TGTGAACCCAGGAGG[G/T]GGAGCTTGCAGTAAG	146691
rs567198426	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17848422	CTAAGACCCCGCTGC[A/T]CCCATCCAGCCCATC	146691
rs567242412	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17855547	CTCCCTGAGAGCCGC[C/T]CGGCCCTAGCCCATT	146691
rs567245428	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17899049	CTCTAGAAAGAGCTA[A/T]AACAACCTGGTAACT	146691
rs567246658	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17958835	GTTGGAACTTTTAGC[C/T]GTACCCTCATCCCAC	146691
rs567253944	in-del	-/G	0.00676609	0.0577691	intron-variant	TOM1L2	GRCh38.p7	17:17855159	GCCATCCTGCTGTCA[-/G]CTGATTCTCACTTGG	146691
rs567284073	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17899768	GTCAATATACTGGTC[C/T]TTCCCAGCTTGCACG	146691
rs567295529	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17881834	CACGACACAACACTG[C/T]CATCCCTACACACAC	146691
rs567305364	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17892296	ACTCCACTTCCTGCA[A/T]TCTCCGCTGCCTCTG	146691
rs567322554	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17907889	CTAGTTGTGTGGTCT[A/T]GGGTAAATTACTTAA	146691
rs567332091	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17944974	TACTCCTGACATTGC[A/G]GCAGATGCTGCCCGC	146691
rs567363561	snp	C/G	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17871354	CCAGACTGGGAGAGA[C/G]AGCGAGACTCCATCT	146691
rs567396924	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17950579	ACTTTGTATGCTCCC[A/G]TTCTAATGAGAGTGA	146691
rs567421895	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17922316	CCTCGGTGAAGGGGA[A/G]CGGTGAGAGGAGGCC	146691
rs567456716	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17913820	ATTCTGCTGCTAAAC[C/T]GAACTTGGAAACGAG	146691
rs567458006	snp	A/G	0.00517822	0.0506191	intron-variant	TOM1L2	GRCh38.p7	17:17908640	AGGACTTCAATAGAC[A/G]TTTCTCCAAAGAAGA	146691
rs567462696	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17862954	TGGGTTTAGGTTCCA[C/T]GGGGAGGGTGGGGCG	146691
rs567472892	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17951160	CATCCATAAATCCTA[C/G]ATGATAATACCCACT	146691
rs567489930	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17914632	TACTGCTTCTGTAAC[A/T]GCCAGCCTGGTGCCA	146691
rs567493479	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17962070	TTTGACATGCTCCAA[C/T]AGAGATGAAACTTGA	146691
rs567521473	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17924343	GTAATGGCTGAACAA[C/T]GCTGTGAATACAATG	146691
rs567561150	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17948252	ATACCAAGATAAATA[C/T]GCCCTAGTCCCTACC	146691
rs567582593	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17878061	GACGCTGACACAGCA[C/T]AAAGCTGCCTCAAGA	146691
rs567600431	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17968960	CTGACTCCTTCAGCA[C/T]TTACAATCTACACCA	146691
rs567606091	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17905996	TCTGTCCCAGGACTT[C/T]TGGGTTTGCTGTTCC	146691
rs567621336	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17870978	TCCCGTCTAGACTGA[A/T]GCTCCTTGAGGGCAG	146691
rs567636715	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17968414	GCTCACTCCTATAAT[C/G]CTAGCACTTTGGGAG	146691
rs567639820	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17910705	CTCCCGAGTAGCTGG[A/G]ATTACAGGCACGTGC	146691
rs567670121	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17932061	GGTACAACATGAATA[C/T]TGTGAGTTCTAATAA	146691
rs567692188	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17864034	ACCACTCGCAGCTAA[C/T]TTTTTTGTATTTTTA	146691
rs567692582	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17873647	GGTTGATGTCAGTCT[C/T]CTCAACAGAGCCCTA	146691
rs567704945	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17891755	CTGTGGTAGAGTGGG[A/G]TGTATGAGGAAGGTA	146691
rs567711780	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17960425	AGCAACCTCTGCCTC[C/T]TGGGCTCATGCCATC	146691
rs567784493	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17953728	GTGTAGTGGGCCTCA[C/T]TGGGTTTCAATCCTG	146691
rs567805069	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17933258	CAGGCAGGAAGAACA[C/T]GAAAGGGCCAAAGGA	146691
rs567811000	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17930066	TGGTTAAGACACTCC[A/G]TTCCAAAAACAAAAC	146691
rs567814784	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17938680	GTCACAAACCAATAC[C/T]ACCTAACCTTTACTG	146691
rs567840230	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17926299	CCAATATCTCTCAAA[A/G]GGCATTTTATTCTGA	146691
rs567846872	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17884355	GCAGGTGCTAATGAC[C/T]CTCACAGGATGGCTC	146691
rs567892455	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17901427	AGTGCTCACAGCCTC[A/G]TGATTTGGCCTCTGG	146691
rs567952808	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17930563	TCAGCTCATCAATAT[C/G]CCATGAAAATGTTTT	146691
rs567963447	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17887245	TTCCAACCCTTATCT[A/G]GGACCTCTGTGCAGA	146691
rs567979192	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17923768	ACTTGGGAGGCAAGA[A/G]GATCACTTAAGCCCA	146691
rs568012941	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17924917	GAATTGTAGTTCCCA[A/G]TGCTGGAGGTAGGGC	146691
rs568037264	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17894886	CAATGAGCTAAGATC[A/G]CGCCATTGCACTCCA	146691
rs568067632	snp	C/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17853173	GAATGTGTGGCCTCT[C/G]GGAGGACGCATGCCA	146691
rs568069284	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17846700	GCTCTTGAGGCAGAT[G/T]TGTGAGGCTACGGCA	146691
rs568100679	snp	C/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17970180	CTGCCTCAGCCTCCC[C/G]AGTAGCTGGGACTAC	146691
rs568135550	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17880272	GCACTTTTCTGCTGC[A/G]GCAAGAATGAGAGAA	146691
rs568158413	in-del	-/AC	0.00318978	0.0398085	intron-variant	TOM1L2	GRCh38.p7	17:17960970	TTTGTGCATTAAAGG[-/AC]ACTATAAACAGAGTA	146691
rs568159775	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17941772	ATGCCTCACTAACTC[A/G]GCTGACTGAAAAACA	146691
rs568172197	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17873268	CATATGCCTATCACC[G/T]AGATTGTACCATTAA	146691
rs568196869	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17917323	TGGGCGACAGAGCAA[A/G]ACCCCATCTCAAAAA	146691
rs568214655	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17851078	GTACACAGAGCAAAA[A/C]AACACAATTGGCACA	146691
rs568215615	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17894840	GGAGGCTGAGGCAGG[A/C]GAATCGCTTGAACCT	146691
rs568242490	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17947466	AGTGATTAAGTTAAA[A/T]TGGGGCCCTAATCCA	146691
rs568279536	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17940303	AGAGTGGCTGGCATA[C/T]AGCAAGAGTAATCAA	146691
rs568285014	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17946836	TTCAAGCCATTCTCC[C/T]GCCTCAGCCTCCCAA	146691
rs568305086	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17886277	CAGTACTGTCAGCCC[A/G]GCTTTCCCTGATGCA	146691
rs568321127	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17939789	AAATGTAATGAAAGT[A/G]TAAGTAAGGGAAAGA	146691
rs568342746	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17962596	TAGGATTAAAGGCAT[A/G]AGCCACCGCGACTGG	146691
rs568355957	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17851448	CACCAGCCCCGGGGG[A/G]ATGCAGGGGGTCTGT	146691
rs568356017	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17845428	GCTCCCCAGGAGGGC[A/G]CCTATTTCAGCTTCA	146691
rs568382503	snp	A/G	0.00478085	0.0486577	intron-variant	TOM1L2	GRCh38.p7	17:17970212	GGCGCATGCCACCAC[A/G]CCTGGCTAATTTTCT	146691
rs568392790	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17846107	AAGTCGCCATCCTGA[A/T]TGCTCCCCAACGACC	146691
rs568392984	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17921840	TCTTCTTCCCCAGAG[C/T]GCCTCCCAGGGGCTG	146691
rs568422411	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17889294	TGCAGTTGGCCAGGG[C/T]GCTACTGATGGCAAA	146691
rs568436106	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17852512	GCCCAAGCCAGTCAC[C/T]GATCAGATTAGGAAG	146691
rs568438834	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17942097	TAACAGCTCCTAAAA[C/T]GAGAGGCAGAAAGAA	146691
rs568440225	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17956011	AAAAACTGCAGACCT[C/T]TGCAGCCAGTGTTAC	146691
rs568441897	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17903681	GAGATCACAGCCTTG[C/T]GGGGGTTGCAGGGCA	146691
rs568442043	snp	C/G	0.00279162	0.0372561	intron-variant	TOM1L2	GRCh38.p7	17:17895706	GGCCACAGGGCCATC[C/G]CTCCCTCACAGCTCT	146691
rs568496001	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17922598	GGTCAGTCTTGGCTC[C/T]CTCTGACCTAGGACA	146691
rs568516429	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17904624	TTGTGCAGCAGGAAG[A/G]GGTAGGAGGGAAGGG	146691
rs568530265	snp	A/G	0.00279162	0.0372561	intron-variant	TOM1L2	GRCh38.p7	17:17918235	AAATTTATGTTATTC[A/G]CTCTAGCAGTTTTTC	146691
rs568561345	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17868318	CCGTAGTCAAAAGAT[A/G]AGACAAGGCCCAAGG	146691
rs568617720	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17950920	AAGAAAGATCAGACA[C/G]TGCAGTTTCTTCTTT	146691
rs568643891	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17859099	ATTTATTTTTGAGAC[A/G]GAGTTTCACTCTTCT	146691
rs568648275	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17881660	GTGGGGTAACAAATC[A/G]CTTGTTCTACTGATG	146691
rs568677898	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17848374	AGGCAGGATGTGAAG[A/G]GCAGGGGATGTGGGG	146691
rs568698190	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17963390	GTCCAAATGGAAACA[C/G]ACCATGCTTGATGTC	146691
rs568749369	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17874056	CGCCTCCCGGGTTCA[C/T]GACATTCTCCTGCCT	146691
rs568752536	snp	A/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17859772	TGTAATACCAGCTAC[A/T]CAGGAGGCTGAGGCA	146691
rs568813238	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17903248	TGTGAGTACCTTAGA[G/T]ACTTCATTCATTTAT	146691
rs568834091	snp	C/G	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17921211	GCTCTGTGTGAGCCC[C/G]AATTCCACACCCTGG	146691
rs568840437	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17912701	CTCCTCACTTCCCAG[A/C]CTGGGCAGCCAGGCA	146691
rs568843536	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17922695	TGGTTAAGATCAAAT[A/G]AGTTAGTGATATAAG	146691
rs568862857	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17965215	TTCCATGCTATTCCC[C/T]TCCCTAGAAGTCTTT	146691
rs568865827	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17853494	TGGGGATAAATCTTG[A/T]GAGCCAACATGCTCA	146691
rs568880206	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17872369	AAAACACAGTGAGCA[C/T]CTGTTCAGGGCTGAC	146691
rs568884510	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17929175	TCGGGACTGTGGCTG[C/T]TCAGCAGCGTCAGGC	146691
rs568917801	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17861336	TGGGTTCCACGGGGT[A/G]TCCCCCGTGGGTCTC	146691
rs568976566	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17904991	GCATCCCGTAGCTGC[C/T]ATACCTCCACCCCTG	146691
rs568986689	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17935400	AGAACTCCTTGATTT[A/T]AATTGGGCTTGCTGC	146691
rs569000272	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17929832	CCTCAGTCAGATACC[A/T]CTTCTGCCCTAGAGC	146691
rs569013626	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17890721	GGCAAGTGGTCATCC[A/G]GAAGGTGGGAGGTTT	146691
rs569024629	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17926996	GGTTGTGTAACTTAT[C/T]AATGACAATGTGACT	146691
rs569124782	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17898799	TTTGTAAATGTAAAA[A/G]ACTGGGAACAAACTG	146691
rs569128363	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17848267	AAGTTTCCCTCCCTG[A/C]GGAGCGGTCTGGCCA	146691
rs569128926	snp	A/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17891001	GAGCTCTTCAGGAAC[A/T]CTGCAAATCTGGAGA	146691
rs569148030	snp	A/T	0.00795532	0.062565	upstream-variant-2KB, intron-variant	TOM1L2, DRC3	GRCh38.p7	17:17973638	TTTATTTATTTATTT[A/T]TTTTTTATTTTTAAA	146691
rs569162167	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17927654	TATGATAATAAGCTG[C/T]TGGCTATACTTTTTT	146691
rs569205334	snp	C/T	0.00318978	0.0398085	intron-variant	TOM1L2	GRCh38.p7	17:17919863	CCTACCATCCCACGC[C/T]CCAGCCGCCAGGAAG	146691
rs569224641	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17875647	CTATTAGAACACCTT[A/G]GTAAATATCCTCTTT	146691
rs569225435	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17877201	CCCAAAAGTGCTTTG[C/T]GATGTGCAGGAGGCA	146691
rs569265074	snp	A/G	0.00238379	0.0344414	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17862424	GGGCCAGGCAGGGTG[A/G]TGTCTGCAGCAGCAG	146691
rs569314407	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17943712	AAATCTGATCTCATC[C/T]TCCCCCTAAGTATTA	146691
rs569385729	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17869914	TCTTTTTGTGGCCAA[A/C]CTAAATAATGCAGCA	146691
rs569407062	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17844891	CTTATAAGGAATCCC[A/G]GCAATAATTTAGTGT	146691
rs569407926	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17883123	AGCAACTCCAAAAGG[C/T]AGCACCGAGAGTGCT	146691
rs569431212	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17848536	GCTGGGCTGAGCACC[C/T]GTGGGTCAGGACCAG	146691
rs569437317	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17950993	CTGTTTCATCTTCCC[A/C]ACTAGGGGGAAGATC	146691
rs569449990	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17936381	CCTGGGCCAGGTTAG[A/G]TGGGGTCTCCATAAA	146691
rs569458316	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17881093	GGGTTGAGCTTTATA[A/C]CCTCAGCACAGAGAC	146691
rs569488871	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17948566	CTAAGGCAGGAGAAT[A/G]ACTTGAACCCGGGAG	146691
rs569488963	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17906165	ACAGGGTTTTTCTCT[A/G]TCACCAAAACTGGAG	146691
rs569507357	snp	C/T	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17850543	CCCCAACACTCCCTC[C/T]CCCAAAAAACCAAAG	146691
rs569570233	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17937154	CCTGGCAAATTGTCC[C/G]TACTCCAGTGGTACA	146691
rs569602190	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17843713	GAGTGGACAGCAAAC[A/G]CGACATTCAACACAT	146691
rs569602648	in-del	-/GTG	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17875370	ACCTGCATGTCCTCT[-/GTG]GTGTCATCACAGCCA	146691
rs569604890	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17951706	GAGTCTGGGCAGCTC[C/T]ACCAGCAGGCATTCT	146691
rs569617130	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17952487	CCTCGACCTTCCCAG[C/G]CTCAAGCAATCCTCC	146691
rs569649889	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17892319	TGCCTCTGCCTGGTT[C/G]CCTCCCTTTGCCCTT	146691
rs569649956	snp	A/G	0.00398564	0.0444627	intron-variant	TOM1L2	GRCh38.p7	17:17900306	GGGTGGATCACTTGA[A/G]GTCAGGAGTTCAAGA	146691
rs569655456	snp	C/T	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17857474	GAAAAGTGAATACTG[C/T]TCGGAGCTCCGGAGA	146691
rs569692233	snp	G/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17885074	CATCCTAAAAAGCAG[G/T]AATTTCCCTAATGGC	146691
rs569724873	in-del	-/T	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17970011	TCTTTCCACTTGCTA[-/T]ATATCCCTATATCTC	146691
rs569725615	snp	A/T			intron-variant, upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17971255	GAACTTTAAGGGATC[A/T]ATCACATCTCATCTC	146691
rs569732619	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17938771	GGTTGAAAGGGTTTT[G/T]TTTTTTTTTTAATAT	146691
rs569767447	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17930636	ATTAACTTTCCTTGT[A/G]ATGGTACAAGAAGGG	146691
rs569793169	snp	A/G			intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17860766	AATCTCATGAGAAGC[A/G]TTAAGACACACATTC	146691
rs569798236	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17914824	AAGTCTTTGAGTCTT[C/T]GAGTGCCAAGTGTGA	146691
rs569836964	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17906913	CTGTAAAACAAAAGA[A/G]GATTCAGGAAATAAC	146691
rs569840269	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17959939	CCGTCTTTTCCTCCA[C/T]CCATCACTGTAGTTC	146691
rs569872029	snp	C/T	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17856908	ACTGTGTTTACAACA[C/T]TGAACTCCCCTGGGC	146691
rs569884681	snp	A/C	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17889645	GTGTGGCCCCTTTAC[A/C]TTGAAAGCTTTTCAA	146691
rs569939974	snp	C/G/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17866041	GCCACTGCGCACGGC[C/G/T]GTGACCTTTCTTTAA	146691
rs569947057	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17871044	GGCTCTCCCCAAGTA[A/C]TTCTGAGAGAATTAA	146691
rs569971782	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17909328	AGCAATAGTCACAAG[A/G]GCCAAAAGGTGTAAA	146691
rs569980052	snp	C/T	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17961689	CCATCCTGGCTAACA[C/T]GATGAAACCCTGTCT	146691
rs570008800	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17899834	TAAAACATTTATACT[C/G]TACCAAATGAAAAGG	146691
rs570017163	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17908770	TAGGATGGCTACTAT[A/C]AAAAAAATAGAAAAT	146691
rs570036234	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17938677	ATAGTCACAAACCAA[C/T]ACTACCTAACCTTTA	146691
rs570040173	snp	C/G/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17858371	TCAAAAACTCCTGGG[C/G/T]GCAAGTGATCCTTCC	146691
rs570069284	in-del	-/A	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17855785	TCCAGAGAAGCTGTG[-/A]ATCCCTTCCTATGTC	146691
rs570071228	snp	G/T	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17851492	GAGATTTTGAAATGC[G/T]TCCTGGTGCATTTCT	146691
rs570072235	snp	C/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17941105	CATTTCTCCAGTGAA[C/G]AGGTGGAAGGGTCAT	146691
rs570073910	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17894252	TAGTGAGTTACTGGC[A/C]CTTATATGTGAGAAA	146691
rs570082658	snp	A/G	0.000551521	0.0165969	intron-variant, missense, downstream-variant-500B	TOM1L2, LOC100507131	GRCh38.p7	17:17857842	CCTCTCTTCTGGGCC[A/G]AGGACAGAAAAGTCT	146691
rs570086106	snp	C/T			intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17860554	TCAGAAGGCTAAAAA[C/T]TGGGACCCAGTAAGC	146691
rs570093858	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17953796	AAAATGCCATCTCAC[A/G]AAGTCAAGAGGGTTA	146691
rs570119776	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17918416	CATGTTGAATAGAAG[C/T]GGTGAAAGGCAGCAT	146691
rs570154265	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17954464	ATTACAGGAACCCAC[C/T]ACCATGTCCTGCTAA	146691
rs570158858	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17945202	GCTAAGAAACAGATT[G/T]CCAGTAGGACCAACA	146691
rs570186302	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17947578	AGAAGCCAAACCTGC[A/C]GCTTGATCTTGGATT	146691
rs570187748	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17878891	TGGGTGTGGTGGAGA[C/T]CTGGGCACTGGCTCT	146691
rs570227922	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17878281	GGAGTGAGGTCTGGG[A/G]ACTAGGGAGAGGCCA	146691
rs570245448	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17896227	TCTAGGATTCTCTAA[A/C]ACCTTCCTCCCAACT	146691
rs570259347	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17962612	AGCCACCGCGACTGG[C/T]CCAATGTGAATATAT	146691
rs570271192	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17970002	GTATCAAGCTCTTTC[C/T]ACTTGCTATATATCC	146691
rs570293006	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17894892	GCTAAGATCGCGCCA[C/T]TGCACTCCAGCTCAG	146691
rs570319593	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17923127	TGTTGGCTGGGCGCA[A/G]TGGCTCACGCCTGTA	146691
rs570331600	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17887275	ACTGGATGAGATGGC[A/T]GCTAACAGAGCAGAT	146691
rs570386834	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17873381	CCACCCCACCCTCCT[C/G]AAGACTCCCAAAGCA	146691
rs570404931	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17895418	TACCTGGACAAAACA[C/T]AGCCGTAAAGAAAGG	146691
rs570408502	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17916456	TTTGCATATGGTATA[A/C]GATAATGGTCCGACT	146691
rs570462959	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17912184	GCACACCTCCCAGAC[G/T]GGGTGGTGGCCGGGC	146691
rs570469573	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17963456	TAGAGCCCCTGGCTG[C/G]AGAGGACCGCTCCGC	146691
rs570472193	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17942978	TAAAGTAATTATTAT[A/G]AAGTAATATGATGCC	146691
rs570480617	in-del	-/T	0.00438332	0.0466095	intron-variant	TOM1L2	GRCh38.p7	17:17961414	ACTACAAAAAAATAA[-/T]TTTTTTTTTAATTGG	146691
rs570503684	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17971099	GGTGTCCACATCCCC[C/G]CTATAGGATTAACAG	146691
rs570550626	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17892958	GCTATAGTCGAGCCT[C/T]CAGACAATGCAACCT	146691
rs570619704	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17846128	CCCAACGACCATGTC[A/G]CTGGTCTCTTCTCCC	146691
rs570652629	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17941186	TTGGGGAGGGGCTAC[C/T]GGCCCCCTGAAGTTC	146691
rs570683564	snp	C/G	1.65315e-05	0.00287498	intron-variant	TOM1L2	GRCh38.p7	17:17879585	CAGTGTACGGTGGAA[C/G]AGCTGCCACCACAGG	146691
rs570691091	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17933430	ACAAAATCAGACTCC[A/G]TCAGAAAAGAAGAAA	146691
rs570755262	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17846602	CAAGGCCTATGCCAG[A/G]GAGCAGAGCAGGGGC	146691
rs570798982	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17965694	CATTGTCTTAATGTC[C/G]CCATCTGAAAATGGA	146691
rs570813598	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17949617	CATCCAAGCCTCACC[C/T]TGCAGGAGCAGAATC	146691
rs570818373	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17897381	TAAGTTTTGGGGTTT[C/T]GCTTGGGCAAAAAAT	146691
rs570824804	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17899932	TAAGAGAAACTGGGC[C/G]GGGCATGGTGGCTCA	146691
rs570825168	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17881972	GAGAGTTTTTTTTTC[C/T]CCCAAGTCTGACCAA	146691
rs570831805	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17942249	TGACCCAAGATCAGC[A/G]TGTTCTTTTTCACAA	146691
rs570836218	snp	A/G	0.0115144	0.0749975	intron-variant	TOM1L2	GRCh38.p7	17:17949693	AAGGACAGAAGCAAC[A/G]GCCAGAAGGCTGGTG	146691
rs570845956	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17939356	ACTTGTGATAGACCT[C/T]AGCAGATTCTATTCA	146691
rs570851544	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17889367	GAAAGGGAATCAGAA[A/G]GTGGGCTGGGGGCAG	146691
rs570851883	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17935513	CCTTGAGCTTGCCGA[C/G]CTGTGCTTTCCAAGG	146691
rs570957714	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17862158	CCTGGGAAAGGTGGG[A/C]AAAAGTGTGTTTCAC	146691
rs570960623	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17936148	TCTCCACCCTCCCTT[C/T]GGCCTCTGGCCTTAG	146691
rs570976310	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17903768	AGTACAACACGGGTT[A/G]TGAAATCATATAACA	146691
rs570992376	in-del	-/T			intron-variant	TOM1L2	GRCh38.p7	17:17873958	TTATTTACTTACTTA[-/T]TTTTTTTTTTTTTTT	146691
rs571081038	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847306	TCTCCATGGGCGGGT[A/G]GAGGAAAGACAGTCC	146691
rs571092897	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17853019	TGTTAACAATGCCTA[A/C]GGCTGGCACTTCCTT	146691
rs571099648	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17958052	TCGAGATTGTGCCAC[C/T]GCACTCCAGCCTGGG	146691
rs571106737	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17859838	GTGAGCCAAGATCGC[A/G]CCACTGCACCCCAAC	146691
rs571115943	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17956623	GGTGAGCTGCAGGTC[C/T]AGAGTCCTGCCCCGC	146691
rs571149803	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17867924	ACCTTTCCCACACTC[A/G]TCTTCAATGAACAAT	146691
rs571163443	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17965333	CCTTCCCAGTCTCAC[C/T]CCCTATCACTCCCCT	146691
rs571176600	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17898273	AAGGAGTTGGTCTCA[C/G]TCTCAGAGCAGGCTG	146691
rs571241214	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17848615	GACATGTTCTTTCTG[A/G]CCTGTTTCCCAATAA	146691
rs571280909	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17898900	GAATAAAGAAACTCA[C/T]GCACCAATATACACC	146691
rs571312756	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17951058	CAACCTAACAAGCCA[A/G]GTAAGGGCTTTAGTG	146691
rs571385286	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17944360	AGTCTGTAAGCTCAC[A/G]GCTGCAGGAGGCTAA	146691
rs571442836	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17920062	CCCTGGCCTCCACAA[C/T]AGACGGTCCAGAGTA	146691
rs571451997	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17875490	ACCCAAGAGCCTACT[A/G]CTTGCTCAGGTCACC	146691
rs571457309	snp	C/T	0	0	intron-variant	TOM1L2	GRCh38.p7	17:17906971	ATGCAGGAGGGGCAA[C/T]GTGTTCTAAGTCCAC	146691
rs571457447	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17915728	GGTCTTGCTATGTTA[C/G]CCAGGCTGATCTTGA	146691
rs571479399	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17921381	TGAGGAGGATCCACA[A/G]ATTTAAAATGCATTT	146691
rs571481718	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17882060	TCATCTAAAAAATCC[A/C]GTGTGGGGTTAAAAC	146691
rs571490515	snp	G/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17868571	GTTGGCCTGATCATG[G/T]TCCTTTCTGGTCCTT	146691
rs571503729	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17891746	AAGGAAGGGCTGTGG[C/T]AGAGTGGGGTGTATG	146691
rs571540993	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17892228	CAGGGAATGGACAGA[A/G]GCTCCTCTCCAGCTG	146691
rs571576452	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17884311	GGGACAACAGGATTC[C/T]CACACCAGATTCTAG	146691
rs571594062	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17877948	CTGTCTGGGTCTGCT[C/T]TGGCTGTCTGGAAGC	146691
rs571612795	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17912896	TCCAGCCGGGGCACC[A/G]CTGAGCACTGAGTGA	146691
rs571712650	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17849828	CTTGCTTCTGTGAGA[A/G]AAGCAATTTCTTTTC	146691
rs571722325	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17870967	CTTATCTGCCCTCCC[A/G]TCTAGACTGAAGCTC	146691
rs571733666	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17960232	ACAAACAATACTAAG[C/T]TCTCTGGTTTAGTGG	146691
rs571783895	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17856445	AGGGCACCAGCCCAA[A/G]CTGGGTGGCAGGCAG	146691
rs571785863	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17863909	CTCACTCTGGATGCC[C/G]AAGCTGGAGTGCAGT	146691
rs571828698	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17944932	CCATTTTTCATAGGC[C/T]GGATGCTCCTGCAAT	146691
rs571844121	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17929191	TCAGCAGCGTCAGGC[A/G]GGGAAGTCAAGAACT	146691
rs571864502	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17903899	GAACAGAAGGGACAG[C/T]AGGTCAGAGGCCTTC	146691
rs571901296	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17930764	AAAGAAGAAATGTTT[C/T]ACCAAGAACCAGAGA	146691
rs571915080	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17877293	CTTCCTATTCCCCCC[A/G]CCTCCTACCCCAGGA	146691
rs571939887	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17929981	GAGGGCTGTCTCTGT[C/G]TCTTTATGAAGACCA	146691
rs571951758	snp	A/T	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17945284	CACACACACACACAC[A/T]CACACACTCTCTCTC	146691
rs571960458	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17923418	AACAACAACAACAAA[A/G]CAACAACAACAACAA	146691
rs571997118	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17877624	CCAACCAGCCAGGAC[A/G]GCTGTGTCTGTTCAC	146691
rs572034790	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17967914	ACCTGTCCAGCTTAC[C/T]CTCTCCCTAAACCAT	146691
rs572036580	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17923925	GGCAGATCATAAGGT[C/T]AGGAGTTTGAGACCA	146691
rs572046618	snp	C/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17864298	TCACTGCAAGCTCCG[C/G]CTCCCGGGTTCACGC	146691
rs572098472	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17878374	GTAGTTACATGGAGA[C/T]AAGTTGTTTCCCGGT	146691
rs572099025	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17850169	TACCCCATGACTCTG[G/T]GCAAGCCACTTCCCA	146691
rs572107476	in-del	-/A	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17896404	CTCCACTCCACTCTC[-/A]AGAGCAACAGTGGCA	146691
rs572122061	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17886645	TTCTTCCTGGCACCA[C/T]TTCATGCCTTTGTAC	146691
rs572156157	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17843981	GGCTGACAGACAATG[C/T]CTCTGGGGTGGAAAC	146691
rs572158808	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17879237	AATACAGAAATAGTA[A/C]AAGCTCAACTACATT	146691
rs572161629	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17915363	TTCAATGATGGGATC[C/T]TGGCTTACCAGGTGT	146691
rs572234198	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17844474	CCAAGGCACCATCAC[C/T]CACATGGAGGCGCTA	146691
rs572244829	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17938359	CCCAGAGAGCTCCTT[C/G]TACCTCTTAGACCCT	146691
rs572246419	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17935862	ACTTCCACCTATCAA[C/T]TTAGCAAATTCTGAG	146691
rs572301710	snp	C/T	0.00199481	0.0315187	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17845601	TGCCCGAGGTCGGAC[C/T]GCCCACCACCCGCAG	146691
rs572320586	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17930281	TACAAACTTTAGCCC[A/G]TTCTCCTAACAAAAA	146691
rs572343374	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17857277	TTCAAGAGGTTTCAA[A/G]TCATTTTGACGGACT	146691
rs572350915	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17961388	TCTGGGATACATGGG[A/G]AGGCCTTGCCACTAC	146691
rs572380660	snp	A/C	0.00119737	0.0244387	intron-variant, downstream-variant-500B	TOM1L2, LOC100507131	GRCh38.p7	17:17858006	CAGCACGTCCCCCTT[A/C]CCTGCCTGGAAAAAA	146691
rs572418704	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17851210	AGGAAGGTGGCTGTA[C/T]GCGTTCTTGAAATGG	146691
rs572447695	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17893328	GGCCCCTGCCCTGTG[A/G]CCTCACCAAACCCGC	146691
rs572450904	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17959348	CATTTGATATCAGAA[A/G]AAAGACAAAAACAAC	146691
rs572457937	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17855293	TTCCAGAGTAAGAGC[A/C]TTGGGGGCCTCCAGG	146691
rs572468592	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17902903	TGGCAACCCCATTTT[A/G]TAAGTGAGGAAATGG	146691
rs572491785	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17846215	GGGAAGGGCTAACTA[C/T]ACCATGGATCAGGAA	146691
rs572506824	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17903399	GAGGCTGAGGCGGGC[A/G]GATCACGAGGTAAGG	146691
rs572522715	snp	A/G			intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17858877	TGAGCCATTGTGCCC[A/G]GCCCTAATTTTTGCA	146691
rs572584175	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17861342	CCACGGGGTGTCCCC[C/T]GTGGGTCTCTCCCCC	146691
rs572585967	in-del	-/GGCTCACTG	0.00438332	0.0466095	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17858651	CAGTGGCACGATCTT[-/GGCTCACTG]GGCTCACTGCAACCT	146691
rs572590366	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17932479	CCCTTTGTTTCCTGG[A/G]GATAGATGAATTATG	146691
rs572605697	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17941576	GATATCCACGGGCAG[C/T]CTAAGTCTTCCCTGT	146691
rs572610189	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17953956	CACTCTCAGGACAGG[A/C]ATAGGACAGGGCAAG	146691
rs572653603	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17947004	TGCTGGGATTACAGG[C/T]GTACGCCACCGTGCC	146691
rs572689004	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17879860	CACTGGGAGATCTGG[A/G]TTGCCTTTCTGAGTG	146691
rs572713066	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17845057	GGGTCTGGGAGCAGA[A/G]ATCTCAGGACAGGCC	146691
rs572734383	snp	C/T	0.00318978	0.0398085	intron-variant	TOM1L2	GRCh38.p7	17:17872701	CTGAGCTCCTCTTTG[C/T]TCCAGCGCTCCAGGT	146691
rs572747826	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17893546	GCACCAAATATTTTA[A/T]ATGTAGAAGTCTCCA	146691
rs572798543	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17955681	AGTCTTGCTCTGCCA[C/T]CCAGGCTAGAGTGTG	146691
rs572821509	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17846878	TTTATTGGTAGTGTC[A/G]TCTCAGCAGCGTGCC	146691
rs572828584	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17910015	GCCTAGGCAACAGAG[G/T]AAGACCCTGTCTCTT	146691
rs572855489	snp	C/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17956179	TTGGTCCATTTTACA[C/G]AGAACTGATTGGTCT	146691
rs572860715	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17879032	CATGGGCTGTCCAGA[G/T]GCGGGGAGGCCAGTT	146691
rs572860812	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17962832	TGGGCGTGGTGGCGC[A/G]TGCCTGTAGTCCCAG	146691
rs572868291	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17846896	TCAGCAGCGTGCCAC[A/G]TGGCCACCATCTGCG	146691
rs572890490	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17896119	GTAACCGTGAGGTAA[C/T]TGGCATTCACTCTCT	146691
rs572896609	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17949302	CGACATTACTGAACA[C/T]CTAGCACGGCAGAGC	146691
rs572912279	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17963991	TGAATGATATGGATA[A/G]CAAGCACTGTGAGCT	146691
rs572975322	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17964733	CATTCCAGCCTGGGC[A/G]ACAAAGCAAGACCCT	146691
rs572984643	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17871960	AAACTCCACAAAATA[C/T]CCACTCTCCTCTGTT	146691
rs573018359	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17865703	GAAATTACTTCAATC[A/G]TAGGGAATGTTCCAT	146691
rs573043163	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17917696	GGCCAGCTCATGCCT[A/G]TAAATCCCATCACTT	146691
rs573086463	snp	C/T	0.00716266	0.059414	intron-variant	TOM1L2	GRCh38.p7	17:17970416	CATTTACTACCTTGT[C/T]ATTTTAAAGGTGTAG	146691
rs573093710	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17866145	GAATTGAAAGTAAGG[C/T]GGTACAACTGGCTAG	146691
rs573104536	snp	A/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17919588	GAGGTCTTAGAGACC[A/T]TCTAGTAAAAAGATT	146691
rs573146800	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17962188	ACTTATATGAGGTTC[C/T]TAGAGTAGTCAAATT	146691
rs573149021	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17971173	TCAGCTTTGGTAAAC[G/T]TAATATGAGGTGGGG	146691
rs573179599	snp	A/T	0.000798403	0.0199641	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17858805	CCAGGACGGTCTCAA[A/T]CTCCTGACCTCGTGA	146691
rs573180082	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17934753	AAGGCAAATAAGAAC[A/G]GCATCCAAAGCAAGG	146691
rs573184467	snp	A/C	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17867350	AAAGGGGGTGGGGCA[A/C]ACATAGGGTGGGCAC	146691
rs573199419	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant, utr-variant-5-prime	TOM1L2, DRC3	GRCh38.p7	17:17973049	ACTCTTTCCTGTGAC[C/T]TTTTTCTCGGAGAAC	146691
rs573224267	snp	G/T	0.00318978	0.0398085	intron-variant	TOM1L2	GRCh38.p7	17:17958980	CAAAGAACTTCCAAG[G/T]TGAACACATAAAGGT	146691
rs573252586	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17868035	CTTGGACTGGGAGAC[C/T]CTTGGGTGAAAATAC	146691
rs573263327	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17882284	CTCACATTCTGCCAT[A/G]GTTTCCTCCCAGATC	146691
rs573269918	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17908978	ACCAGGTCAGGAGAT[C/T]GAGACCATCTGGCTA	146691
rs573276841	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17920251	ACATCTTTTATTTTG[C/G]AATAATTTTATATTT	146691
rs573323113	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17942817	TCCAGGAAAGGCTTT[C/T]GCCAGCTTTAGTCGC	146691
rs573325798	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17883255	GTACCATAAGAATTA[C/T]TTTTTTGGTCTTTAC	146691
rs573340585	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847346	GCTCAGGAAGCACTG[C/T]CTGGGGCTGGGCCAC	146691
rs573361082	snp	C/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17896783	AAGCAGAGAGCCCCT[C/G]AGGGCTTCTTACTAA	146691
rs573362153	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17876123	AAATTGGGAGAGACA[C/G]AGGACACTGGATGAC	146691
rs573364417	snp	C/T	0.00358779	0.0422022	intron-variant	TOM1L2	GRCh38.p7	17:17883811	ACATTAAAATTAAGT[C/T]GTGTTCCTACGAGAG	146691
rs573485934	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17965414	CCAGCATTTGCTCAA[A/G]TTGTCTCTGCCAAGA	146691
rs573500823	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17880814	CTACTACACACATAC[G/T]GCCCTTGTTCCTGCT	146691
rs573528118	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17881569	GGGCCAAAAGCCAGA[C/G]ACCTTCTTTCCCACA	146691
rs573541129	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17854332	CCCTGGTTGGAGCAG[A/G]GGGCACTGCGCTGAG	146691
rs573549413	snp	A/C	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17957057	AATCATAGCTCGCTG[A/C]AGTCTCCACCTCCTG	146691
rs573557675	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17891405	GTGTGGAGGGGTGAT[C/T]CTGATAGGAAAGCTT	146691
rs573569666	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17891826	GTGTGTGTGTCAGAG[A/G]GAGACAGAGAGACAG	146691
rs573577662	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17854820	ATTACAGATGTGAGC[C/G]ACTGCACCCAGCCTG	146691
rs573613920	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17848697	CCACCCGTGAAGCCC[A/G]TGGCTCAGGGCCTGG	146691
rs573618813	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17942645	GAGGCTACTTAGTAG[A/G]CTCAGAGTAAGTAAT	146691
rs573646540	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17843857	AAGCAGTTCTGACTC[A/G]GGGGCTGATGGCTGC	146691
rs573661313	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17953184	ACTTAGGAGGCTGAG[A/G]CAGGAGAACTGCTTG	146691
rs573663196	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17907042	CCTGGACCTCCCTCC[A/G]TGGACACGGTGGTGC	146691
rs573719702	snp	A/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17936669	TTATGTAGTCATTTA[A/T]TAATGATATTTATAA	146691
rs573754378	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17928835	CCCACCCACAGTAGC[C/T]ATTCAGGAAAGGCAT	146691
rs573756980	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17937354	AATAAGGAAATGGTA[A/G]CCTGTGTGCCAATAT	146691
rs573795435	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17861619	GAGGGATGGGGTAGT[A/G]GCCTGTAATCACTTC	146691
rs573796235	in-del	-/GTGA	0.00676609	0.0577691	intron-variant	TOM1L2	GRCh38.p7	17:17903234	ATTCCTCATCAGACT[-/GTGA]GTACCTTAGAGACTT	146691
rs573797797	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17938401	ATTTCACTGCAGTGG[A/C]CTGAAGCTGCCTTCT	146691
rs573807742	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17900425	TACTCTGGAGGCTGA[C/G]GCAAGAGAATTGCTT	146691
rs573836349	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17900561	AAGAAAGAAAAAAAG[C/T]TTAAGGAGCAAGGCT	146691
rs573839870	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17950666	GATTTCAATGTATTT[A/C]TTTATTTTAATTTTT	146691
rs573843462	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17912942	CAATCCCGGCACCTC[A/G]GGAGGCCGAGGCTGG	146691
rs573880157	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17905204	GGTGAAAATATGCCA[C/T]CTTTCACCAAAGACT	146691
rs573895744	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17876735	GCCCAGCTCATCAGT[A/G]GGAGGGCAAGGATGG	146691
rs573917655	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17898339	CCTCTGCTCTGGGCT[C/T]CTGTACCTGACAGCA	146691
rs573967615	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17870134	GACTGCATTAGGTAT[A/T]TTTTGGTGGCACGTC	146691
rs573995927	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17912661	CTCCTCACTTCCTAG[A/G]TGGGATGGCGGCCGG	146691
rs574051704	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17946036	ATCACGCCTGCCTGG[C/T]TAAATTTTTCATATT	146691
rs574097240	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17844491	ACATGGAGGCGCTAA[C/T]AGAAAGACAGGAGGA	146691
rs574119126	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17892501	GGTCTGCACACATCC[C/T]AGCTCAGAGCCCTTC	146691
rs574123814	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17856538	CGCTTTGCTCAAGCA[G/T]GTGGACCCTGTGCTG	146691
rs574132087	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17951985	TTTCCAATACTCTTA[C/T]AGTCTGACATGAGCA	146691
rs574144301	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17952943	GGTTGAAAAGGTGTA[C/T]ACACATTCTCAAAAG	146691
rs574145618	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17961493	GGCAGGAGGATTGCT[C/T]GAGTTCAGAAGTTCG	146691
rs574160833	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17850255	GTGCTTTGTAAAGAA[C/T]AGAGGGAGGGGCCAG	146691
rs574183956	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17876878	TGGGGACACGCAGAA[A/C]GACCCAACAGATAAG	146691
rs574197575	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17850637	AGCTACGGCTAGGAC[C/T]GTGTGGGTGAAGGAG	146691
rs574207754	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17954048	TAATTATTAAATACA[A/T]ATAAGTTATAAGTGC	146691
rs574223632	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17967520	ATTTTGAAGCTTGTT[A/G]CAGAACAGAAAATTA	146691
rs574239650	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17923239	CCTGGTCTCTACTAA[A/G]CATACAAAAAAATTA	146691
rs574247504	snp	A/C/T	3.30105e-05	0.00406256	missense, upstream-variant-2KB, intron-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17862734	GGCCCCACATACGTC[A/C/T]TGCGCTGCTCAGCCA	146691
rs574269700	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17914295	GGCACACTGCTGTCT[C/T]AGTGGCTACATTGTG	146691
rs574277184	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17915124	TACAGAGGTCTTCTA[G/T]GTTATTATCTGAGTA	146691
rs574329339	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17916053	TTGCTAAATCCAATG[C/T]CATGATTTCCCCTTT	146691
rs574335842	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17958401	ATGAGCTAATTTCAT[G/T]TAAACCATCAAATCT	146691
rs574349810	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17968607	GGGGCGGAGGTTGCA[G/T]TGAGCTTAGATCGTG	146691
rs574390412	snp	A/C	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17969279	TCAGGCTGGCCTCCA[A/C]CTCCTGACCTCAAGT	146691
rs574404512	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17931506	ACACAGGAGTCCTCA[A/G]GAGAACTGGGGGAGC	146691
rs574411279	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17864369	CCGCCCACCACCACG[C/T]CTGGCTAATTTTTTG	146691
rs574423054	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17864678	CACCATGCCCAGCTG[A/C]TTTTTGTATTTTTAG	146691
rs574457360	snp	C/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	TOM1L2, LOC100507131	GRCh38.p7	17:17858114	CTCCAGGAGATCACA[C/G]AAGGTTGACCAGAGC	146691
rs574485021	snp	C/T	0	0	intron-variant	TOM1L2	GRCh38.p7	17:17879053	GAGGCCAGTTTGCAA[C/T]GGCAAACCACAATAT	146691
rs574485098	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17871142	ATTGGAGGCCGAGGC[A/G]GATGGATCACGAGGT	146691
rs574524693	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17893297	CCCCTTACCTTGCTC[C/T]GCCTGACCCAGAGTT	146691
rs574657118	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17851368	TCCGCTGTCAAGCCC[A/G]ACCCAGGGAAGGCCA	146691
rs574717588	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17954604	AAGTGTGAGCCACCG[C/T]GCCTGGCCCTATTTA	146691
rs574737657	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17851258	AGTGTCCACTCTCAC[A/G]TTGCGGGGCCTCTCA	146691
rs574798401	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17888366	ACAAACATAAACCAT[A/C]ACCTATTCATTTCTG	146691
rs574815478	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17941496	TGAGAATCATCATTA[C/T]GCTGACTCCCATTAA	146691
rs574834058	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17953632	GATGGGGTGTAGAAA[A/C]AGCCCACAGCTGACC	146691
rs574845033	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17932640	GGATGTGGTGGGGAA[C/T]GTACTTTGGAACCAG	146691
rs574862191	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17903928	TCAGGGAGGGCACAA[A/C]GGGGTGGGTGGGGTG	146691
rs574880243	snp	A/C	0.0115144	0.0749975	intron-variant	TOM1L2	GRCh38.p7	17:17931597	GAGCTCCTTGAAAGG[A/C]AATACAATGAAGCAT	146691
rs574898892	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17896899	ACTAAGAGAGTAAGT[A/G]AAGCCCTATCAGCAG	146691
rs574938522	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17919076	TCTAGAACAGGGAGT[A/G]TGAACTCAGATTTTG	146691
rs574972227	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17951637	TTCAAGAAACGTAAA[C/G]GTCTTGCATAGCCTT	146691
rs575001655	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17926423	TGGCACAAGGGGAGA[C/T]GCGGACATAAATGTA	146691
rs575018759	snp	G/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17947758	GCTCAGGCTCAAAGA[G/T]GTTACTGGAGCTGGG	146691
rs575023206	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17858538	TCTCTGTCTCAGCCT[C/T]CCAAGTGGCTGGGAT	146691
rs575025272	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17947015	CAGGCGTACGCCACC[A/G]TGCCAGCCTAAGTGT	146691
rs575188500	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17903485	GGGCGTGGTGGCGGG[C/T]GCCTGTAGTCCCAGC	146691
rs575207125	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17921601	CCAGGCTTTGGGGAA[C/G]AGGGGGCTGTGGCCA	146691
rs575234195	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17942453	AAAACTATATACTTC[A/G]CAGGATTACTATACT	146691
rs575238899	snp	A/G	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17853414	CAGATTTTTCTTGTA[A/G]TTGTTTTGTTGCTGC	146691
rs575247946	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17895061	GATGACCATGATTAC[A/G]TGATTACTGTTCAGA	146691
rs575285624	snp	C/T	0.00318978	0.0398085	intron-variant	TOM1L2	GRCh38.p7	17:17869176	CAGGAGGACAAGAAG[C/T]ATTTTTCCTGTCAGC	146691
rs575288829	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17957282	CACCACTCCCTTATA[C/T]AGCCTTTCAAAATGG	146691
rs575299940	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17918516	ACCCATTTGAGTCCT[C/T]ATTCCATAAAAAATT	146691
rs575321226	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17943221	CAGGTCTCAAACTGG[A/G]GTATGTTCTGTCCCC	146691
rs575359229	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17949320	AGCACGGCAGAGCAT[A/G]GAGCATAGGGCCCAG	146691
rs575366724	snp	C/T	0.00279162	0.0372561	intron-variant	TOM1L2	GRCh38.p7	17:17956617	AGGCATGGTGAGCTG[C/T]AGGTCCAGAGTCCTG	146691
rs575394241	snp	A/C	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847449	AGTTGTCCCACCACT[A/C]AGAGAAAAGAAGTGG	146691
rs575400156	snp	A/T	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17949847	TGTTCTCTCTCTCTA[A/T]TTTTTATTTTTATTT	146691
rs575408509	snp	A/G	0.0023933	0.0345097	intron-variant	TOM1L2	GRCh38.p7	17:17914199	GAAGAGCAGGGGCAG[A/G]AGGCAGGCACCATTT	146691
rs575429598	snp	C/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17847938	CGTGAGCTGCAGTGT[C/G]GGGGGAGGCTCCTGG	146691
rs575434619	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	TOM1L2, DRC3	GRCh38.p7	17:17972380	TCCGCTGTAACCCGC[C/T]GGACTCCCGTCCTGA	146691
rs575450758	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17879377	TTCTTTCTGTGAGCA[G/T]GTATTCTACAACTGG	146691
rs575466317	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17946263	GTACAATTCAGTGGC[A/G]TTAGTACATATATTC	146691
rs575486968	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17919119	TCTGCCAATTACTGT[A/G]TGACTACAGGCAATA	146691
rs575501141	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17860087	AAGGCAGGTCCTGGA[C/T]CCAGAGTGAGGGACA	146691
rs575523765	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17911333	AGCCCAGCCTGGCCT[A/G]CCCTACCCAGCCTCT	146691
rs575530965	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17964916	CAGGCTGACGCCCCA[C/T]GTGACTTTCAATGTC	146691
rs575566265	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17920585	CCTCGTGATCCACCC[A/G]CCTTGGCCTCCCAAA	146691
rs575586184	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17861024	ATGTGGCTCGGGTCA[G/T]CATTGTCCTTCCTGG	146691
rs575603617	snp	A/T	0.0310518	0.120672	intron-variant	TOM1L2	GRCh38.p7	17:17912977	TCGCTCGCGGTTAGG[A/T]GCTGGAGACCGGCCA	146691
rs575624454	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17956310	AACTAGATACAGAGT[A/G]CTGATTGGTGCATTT	146691
rs575636578	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17965583	CTGAGGGCAGCACAG[C/T]GTGACAGGATACCAG	146691
rs575663985	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17958066	CTGCACTCCAGCCTG[G/T]GCAACAGAGCAAGAC	146691
rs575668904	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17861733	TCTGTCTCCCTGCAG[C/T]GGATGCTAGGAGGCC	146691
rs575689662	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17869689	TTTCAGCAGACAAAT[A/G]TCCAGACATACTGTT	146691
rs575704262	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17875692	ATCCCAATGCCTTTA[G/T]CTTTTCTTCAAGGGA	146691
rs575705094	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17854977	GAAGGAAGCTAGCAG[A/G]GGAATGCCCTCCAAT	146691
rs575708864	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17949322	CACGGCAGAGCATAG[A/G]GCATAGGGCCCAGTG	146691
rs575723523	snp	A/G			utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	TOM1L2, DRC3	GRCh38.p7	17:17972381	CCGCTGTAACCCGCC[A/G]GACTCCCGTCCTGAC	146691
rs575731299	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17881682	CTACTGATGGGAGAC[C/T]GGGGTTAAATGTCCT	146691
rs575738272	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17905325	AAAGATCTACTGCTG[A/C]TCTCTGCTCCCCAGC	146691
rs575740518	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17868897	AAGGGAAAAGCTTTT[C/T]TTCTTTTTTCTTTTT	146691
rs575777331	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17890163	CTCAAAGGGGCTAAA[A/G]AAAGGTTGACCCAAT	146691
rs575804931	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17933732	TCTTTCCTTCCCCTA[C/T]AAGTCACCCAGAAAA	146691
rs575816616	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17882358	GCTCCGAGAGAGCAG[C/T]GTCTGCATCTCTGCA	146691
rs575867014	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17929194	GCAGCGTCAGGCGGG[A/G]AAGTCAAGAACTGCC	146691
rs575912439	in-del	-/TATTAT	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17910562	TTCAGTGATTATTAC[-/TATTAT]TATTATTATTATTTT	146691
rs575914792	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17849357	CATGAGGCCTTGATG[G/T]CTCAGGGCCACAAAG	146691
rs575916735	snp	A/G	0	0	downstream-variant-500B	TOM1L2	GRCh38.p7	17:17843344	CACAACCTGGGCCAC[A/G]CACAGGAATTTTCCT	146691
rs575968457	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17884401	TTCCATGAAAACCCT[A/G]AACTGATCCCTTTAT	146691
rs576008643	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17876841	TTTGAAAGCAAGAGG[A/G]CTGCTGTGAACAGCC	146691
rs576048505	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17893412	GGCCACCCTACCTGC[C/T]TTTGTGAGCAGCAGA	146691
rs576055554	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17930246	TGCTCCAGAAAGTGG[A/G]GTATAGAGAATTACC	146691
rs576124176	snp	C/T	0.00279162	0.0372561	intron-variant	TOM1L2	GRCh38.p7	17:17906207	GCTCATGGCTCACTG[C/T]AGCCTCGACCTCCTG	146691
rs576165588	snp	A/G	0.000798403	0.0199641	intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17858503	CTCACTGCAACCTCC[A/G]CCTCCTGGATTCAAG	146691
rs576225554	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17870242	CCCCTGGAGCCCTCT[C/T]TACCCTTAGAAGCAA	146691
rs576286385	snp	C/G/T	0.000148296	0.00860985	intron-variant	TOM1L2	GRCh38.p7	17:17898557	CAGGAGCAAGGAGTT[C/G/T]CCCAGATGACTTCTC	146691
rs576298613	snp	G/T	0.00557542	0.0525036	intron-variant	TOM1L2	GRCh38.p7	17:17864210	TAGCAGAATCCAATT[G/T]GATTTTTTTTTTTTT	146691
rs576308406	snp	G/T	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17937449	AGGGGACTTTCACAG[G/T]TAAGAATGGTGAGGG	146691
rs576324020	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17891514	CTGCCCTCAGCCATG[G/T]TCCCCACACAGTCAG	146691
rs576340001	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17900645	GACATATGGCTGCCC[C/T]GTAGGAATTCTTGGC	146691
rs576355325	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17958474	AGACTAACTTTCAAA[C/T]AATAAAATGTATTTA	146691
rs576401691	snp	C/T	0.00398564	0.0444627	intron-variant	TOM1L2	GRCh38.p7	17:17874323	TCACCCAGGCTGGAG[C/T]ACGGTGGTACGATCT	146691
rs576408894	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17850697	GTTGGCCTCCGCAGG[C/T]CGGGAGGCCACTGCA	146691
rs576425947	in-del	-/T			intron-variant	TOM1L2	GRCh38.p7	17:17915843	TTAAACTGAGTAGGT[-/T]TTTTTTTTTTTTTTT	146691
rs576466470	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17939177	GCCAGCCCTCTCTAG[C/T]GTGACTTTCTCTCCC	146691
rs576476246	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17854644	ATCCTTGTGCCTCAG[C/T]CTCCTGAGTAGCTGG	146691
rs576499620	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17931146	ACAAAGAACTACACA[C/T]TCAACCAAACCAGAC	146691
rs576523236	in-del	-/AGC	0.00199481	0.0315187	downstream-variant-500B	TOM1L2	GRCh38.p7	17:17843058	GTCTACCTGGCTTGG[-/AGC]AGCAGTTCTCAAATT	146691
rs576551559	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17946138	CTGCCTCAGCCTCCG[A/T]AAGTGCTGGGATTAT	146691
rs576595976	snp	C/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17844998	ACAGAGCCGCACCCC[C/G]TTCCTGGACCAGGCA	146691
rs576610448	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17929693	TTTTCAGAGCAGTAG[C/T]TAACTTTTTGGATAA	146691
rs576611020	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17851715	AGCTCCCTTTAGTCT[C/T]GTCCTTTCTTCCCTG	146691
rs576633754	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17845541	GGCTCTTCCCTCTGA[G/T]GACACTGGGTCTGGG	146691
rs576649110	snp	C/T	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17856606	CAGCCTAGCATAGCA[C/T]ACTATGGGCAGTTAT	146691
rs576675668	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17857233	GCTGGGATTACAGGC[A/G]TGAGCCACTGCACCC	146691
rs576693968	snp	A/G	0.00199481	0.0315187	intron-variant	TOM1L2	GRCh38.p7	17:17899097	AGGGAACCAAAGGCG[A/G]AGGGAGGTTTTTCAC	146691
rs576710587	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17907975	GAAAATTAAATGGGT[C/T]GATATACATGAAACA	146691
rs576718243	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17854284	GGAGGCCGAGGACGC[A/G]CTCCTTGTCAGGCTG	146691
rs576720331	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17924947	CCTGGTGGGCAGATC[C/T]TTCATGCCTTGATGA	146691
rs576756078	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17892576	TGCATGGCCACTGGC[A/C]TCTGGGCATCCTTCT	146691
rs576763749	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17925673	ATAGCGACCTCACCT[C/T]GTGTCTACCAAAAAA	146691
rs576764362	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17952205	AAATGTACAATGACA[C/T]GGCAAAACAAAAGCG	146691
rs576771158	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17909942	GCTGAGGCAGGAAGA[C/T]TGCTTAAGTCCAGGA	146691
rs576806965	snp	A/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17962029	CACACAATGGAATAT[A/T]ATACAGCCTTAACAA	146691
rs576833337	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17971544	AAGTCCCGGAGCAGG[A/G]GGCATTTCTGGGAGG	146691
rs576843100	snp	A/C	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17926973	GGCTAACAGACTTAT[A/C]ACACACAGGTTGTGT	146691
rs576875573	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17851846	ACTAAGGTGTACCAC[C/G]GGGTTGCCTGAGCAG	146691
rs576886754	snp	A/G	0.00159617	0.0282053	intron-variant	TOM1L2	GRCh38.p7	17:17903350	AGTAATTGGCTGGGC[A/G]CGGTGGCTCACGCCT	146691
rs576887331	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17970279	CCGTGTTAGCCAAGA[C/T]GGTCTCGATCTCCTG	146691
rs576888169	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17892006	CCTGGGGACAGCATG[C/T]CCCTGGGTTCTTAGG	146691
rs576894860	snp	C/T	2.85923e-05	0.00378091	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17866397	AGGTCTATTAAGTTG[C/T]CTTCGGTTACTTCAT	146691
rs576910448	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17902775	AATCTTTAAAGTGAA[A/G]TAGTACATCCACATA	146691
rs576929620	snp	C/T	0.00636936	0.0560724	intron-variant	TOM1L2	GRCh38.p7	17:17867083	ACTCTGCCACGGCTT[C/T]CTCTGTGTGGGGCTC	146691
rs576961436	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17878548	GGGCACAATAAGCAG[C/G]AACTTGGGACCAGGA	146691
rs577038723	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17870019	TTTCTAGGTGAAAGG[C/G]TATGGTCATTTATAA	146691
rs577068501	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17948663	CCTCAAAAAAAAAAG[A/G]TGGCCCTTTCTTAGA	146691
rs577126265	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17934703	AAATAACAATATGCG[A/G]TATTTCATCTTATCT	146691
rs577160085	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17880606	CACTCAGTGACAAGA[C/G]ACCAAATAACGCTGG	146691
rs577181117	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17969405	TGTTATTTTATTTCT[A/G]TATTCCCCCTCCCTC	146691
rs577199124	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17881396	CCTGTGCTACCTATG[C/T]CCAGACCCTGCAGAC	146691
rs577262928	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17927125	TTTTCCTAGCTTTTC[A/G]GATTTTTACTGTAGA	146691
rs577271112	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17882405	GAGCATGCGGTCTCA[C/G]CTGACAAAGCCCAAC	146691
rs577272955	snp	G/T	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17891363	GGTTAGCAGCAGGAC[G/T]GGGTAAAAGCTAGGA	146691
rs577345336	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17887881	TTCTCACAGTTACTA[A/G]GCATCCTTATTTTCC	146691
rs577414052	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17852594	AATTGAGCAGGGCAC[A/G]GTGGCTCATGCCTGT	146691
rs577414962	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17918725	TGGGCTCCAGCACCT[A/G]ATAGTACAGTTCACA	146691
rs577435112	in-del	-/G			intron-variant	TOM1L2	GRCh38.p7	17:17938771	GTTGAAAGGGTTTTT[-/G]TTTTTTTTTTAATAT	146691
rs577453929	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17846814	GTCCCTCCACAAGCC[A/T]GGACCAGGTGTGCGG	146691
rs577497915	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17895122	CCTCTTATCCTCCCA[C/T]AGGACAGGTATGTAG	146691
rs577517073	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17847981	CTCCTGCCCTGGAGG[A/G]AAAGGCTCTGGAAAA	146691
rs577528780	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17887520	GAGCTGTCCCCCAGG[C/T]TGGAGTACAATGGTG	146691
rs577551479	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17897804	CCTCAGTTTCATCAT[A/C]TGTACGGGGGAGGAT	146691
rs577567145	snp	A/C/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17923414	CTCAAACAACAACAA[A/C/G]AAAACAACAACAACA	146691
rs577681055	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17938946	CTAAATGACTTGCCC[A/G]GACACACACACAGCA	146691
rs577685554	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17928134	TCTTTTTCCTTTTGT[A/G]TATGTCTGAAATTTT	146691
rs577688367	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17936489	ATTCTATTTAAAGGA[A/G]TTTATTATATGTAAA	146691
rs577721082	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17929056	AAGTCTGAAGATTCC[C/T]CAAGCACTGCTGTGA	146691
rs577746773	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17963740	CTGTGAAGGTCACAA[A/G]GAAACAGAAAGTAGA	146691
rs577755143	snp	A/C	0	0	intron-variant	TOM1L2	GRCh38.p7	17:17943285	TCACTTTAAAAAACC[A/C]TTTCTTCTTTCCATC	146691
rs577794307	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17943775	ATAAGGTCTACACTC[C/T]TCAACCTGATCCTCA	146691
rs577805640	in-del	-/ACAGCCAAGAC	0.00159617	0.0282053	upstream-variant-2KB, intron-variant	TOM1L2, DRC3	GRCh38.p7	17:17973136	TTACAGTCGTGTGAG[-/ACAGCCAAGAC]ACTTTAGTCCTGGGC	146691
rs577814180	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17964654	TCCCAGCACTTTGGG[A/G]GGCTGAAGCGGGAGG	146691
rs577837844	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17853495	GGGGATAAATCTTGA[A/G]AGCCAACATGCTCAG	146691
rs577883714	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17854274	AGAAACTGTGGGAGG[A/C]CGAGGACGCGCTCCT	146691
rs577912547	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1L2	GRCh38.p7	17:17921752	AGGGAAAGTGGGGGC[A/G]GGGTGGGGGGGTGGG	146691
rs577917773	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17904695	CAGAGAATGCAGCAC[C/T]TGACCTTGACTACCT	146691
rs577923228	snp	G/T	0.00636936	0.0560724	intron-variant	TOM1L2	GRCh38.p7	17:17912372	CTGCCGGGCGGAGAG[G/T]CTCCTCACTTCTCAG	146691
rs577942173	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17957485	CTTTCTGGGGTGAGG[C/T]TGACAGTGCGTATCT	146691
rs577950638	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17899896	GGGGAAAGGGTTGAT[A/G]CTCTGCTAATCAGCT	146691
rs577951815	snp	A/G	0.0209421	0.100162	intron-variant	TOM1L2	GRCh38.p7	17:17913074	TGCCTGCAATCGCAG[A/G]CACTCGGCAGGCTGA	146691
rs577952743	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17863011	CCACATGCCGGAGGA[C/G]CCAGGGCGGGCCAGA	146691
rs577976972	snp	A/C	0.00279162	0.0372561	intron-variant	TOM1L2	GRCh38.p7	17:17906219	CTGCAGCCTCGACCT[A/C]CTGGGCTCAAGTGAT	146691
rs577991731	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17897806	TCAGTTTCATCATCT[C/G]TACGGGGGAGGATAG	146691
rs578004342	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17941994	ACTTTCCCACAAAAA[C/T]GTAGCACAAAAGAGC	146691
rs578006170	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17958307	TCCCAGACTTTCCCA[A/G]TCCTAGCCTGGGATT	146691
rs578014236	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17951291	CCAGTCTCTGAGAAC[A/G]TTCATAAGATTTAGA	146691
rs578046803	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17956756	GCCCCTCACTGCCCG[A/G]GGCCTGCGGTGCTGG	146691
rs578048543	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17951862	CCCTCCTCAGATGTG[C/T]AGAAATTAAAAGATG	146691
rs578059808	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17849476	GCACCAGCCTCCTCC[C/T]GTGGCCCAGATTATA	146691
rs578085701	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17899254	GACACAGAAGAGAGC[A/G]TGCCAGGTCCTTGTG	146691
rs578098456	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1L2	GRCh38.p7	17:17855011	GACTGCTGCCTGAAG[C/T]TCAGCCCCTCTGAAG	146691
rs578101726	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17862537	TGTGTGTGTGTTTGG[C/G]GGGGTGGGGGAGGAG	146691
rs578147042	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17875972	GAAGCAAGAGGAGAT[A/T]CACCATCTGCTACTT	146691
rs578191280	snp	A/G	0.000115637	0.00760295	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17869419	CCTCATTGGACACGC[A/G]GGAGATGAGCTCCAC	146691
rs578211185	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1L2	GRCh38.p7	17:17922678	TACCTCCTCACAGGG[A/T]GTGGTTAAGATCAAA	146691
rs578254737	snp	A/T			intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17859097	TTATTTATTTTTGAG[A/T]CGGAGTTTCACTCTT	146691
rs745306136	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17916219	GCTGAGACTACAGGC[A/G]CCCACCACTATGCCA	146691
rs745307064	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17877852	AGGAGATTAGGTTCT[C/G]TTTGTCTTGGCTGAT	146691
rs745316269	in-del	-/ATT			intron-variant	TOM1L2	GRCh38.p7	17:17868653	GGAACTGTGCTTGCC[-/ATT]ATTCCTCCTATTTAA	146691
rs745316506	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17944697	TAAAACCAACGTCTC[C/T]TACAAGGAGAGGTGA	146691
rs745333988	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17932085	CTAATAACTCACAGG[A/T]GACTATTCTAGTACT	146691
rs745341044	in-del	-/GT			intron-variant	TOM1L2	GRCh38.p7	17:17891786	AGTGCATGCACACGT[-/GT]GTGTGTGTGTGTGTG	146691
rs745366951	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17899508	TTAATTACTCTTATA[C/T]CTTAGAGTCAGGATT	146691
rs745368133	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17882997	GCTCCACTGCTGCCC[A/G]GGTGAGGTTCACAGA	146691
rs745400911	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17945062	CCATTAATCAGGGCC[A/G]TGGACACCAAAATAG	146691
rs745418480	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17898522	TGGGCAGAGGGAAGG[C/T]CCTGTGAGGGGGGCA	146691
rs745464985	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17879547	CCCGCCTTGCCGCTG[C/T]GTCCCCGGGTGGGAT	146691
rs745464991	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17862968	ATGGGGAGGGTGGGG[C/T]GGGACTTTCCTTGGT	146691
rs745485659	in-del	-/C	1.65209e-05	0.00287405	intron-variant	TOM1L2	GRCh38.p7	17:17847823	CAGGGTTGGTGAGGG[-/C]CAGGCCACCAGAGGA	146691
rs745506066	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17944547	AAAGGTCACAAGACA[A/G]ACTAACGCAGACCAT	146691
rs745531283	snp	C/T	6.59718e-05	0.00574296	intron-variant	TOM1L2	GRCh38.p7	17:17884799	GCCTGTTAGGAAGCA[C/T]TTCTCAGAGCTGCCA	146691
rs745534671	snp	A/G			intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17860949	CAAACCCTGGCTCTC[A/G]AGTGCCTTCTAATGG	146691
rs745542210	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17910616	ACTCCATTGTGCAGG[C/G]TGGAGCGCAATGGTG	146691
rs745557175	snp	A/G	1.6473e-05	0.00286988	missense, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17884735	GCACAACGCCGGTGA[A/G]ATCAGGACTGCTTCG	146691
rs745559062	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17956379	TTTACAATCCCTTAG[C/G]TAGACATAAAGGTTC	146691
rs745590174	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17893071	TCCGTTTGAAGGTAT[A/G]TTTTGAGGTAATTTG	146691
rs745605701	snp	A/C/G/T	6.63027e-05	0.00575743	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17869349	TCCCACCTCTCGTAT[A/C/G/T]GAAGGAAGACGTTGT	146691
rs745618875	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17906964	TGCAGGAATGCAGGA[A/G]GGGCAACGTGTTCTA	146691
rs745639899	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17855589	TTTCTCTTCAACCAG[C/T]AATAAGCCTGGTGGT	146691
rs745655410	in-del	-/AC/ACAC			intron-variant	TOM1L2	GRCh38.p7	17:17945267	ACCACACACACACAT[-/AC/ACAC]ACACACACACACACA	146691
rs745658152	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17856858	GAGACCCTTGCAGGT[C/G]TGTGGGCCAGGAAAG	146691
rs745665118	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17952806	AAGACCAAAGAGAAG[A/G]CAGCCTCTGGGGTAG	146691
rs745712804	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17905707	CTATGCCAGGCCATC[A/G]CTGGGTTTTCTGCAT	146691
rs745722018	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17921662	ATGTCAGACAGGTGG[A/G]GGTGGCTGGGAGGAT	146691
rs745747417	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17879871	CTGGGTTGCCTTTCT[A/G]AGTGCACACTGCAGA	146691
rs745778205	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17966359	TCTAAATAATCACTC[A/T]TTTAGCCTGTCCACA	146691
rs745783615	snp	C/T	1.64933e-05	0.00287165	intron-variant	TOM1L2	GRCh38.p7	17:17850969	TATGGAGGCGGCAAG[C/T]AGCGGGCCAGGCAGC	146691
rs745797143	snp	A/G	5.70131e-05	0.00533885	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	TOM1L2, DRC3	GRCh38.p7	17:17972266	CGCGGCCTTACCGAG[A/G]CACTGCCCCACTGGT	146691
rs745811169	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17955963	ATTGTTCATTCCTCC[C/T]AATGGGTTCGTGGTC	146691
rs745815982	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17849756	TACTGGACACATCCC[C/T]TCCCTGTCTGGACCC	146691
rs745829131	in-del	-/T			intron-variant	TOM1L2	GRCh38.p7	17:17907028	GTCTGCCCCATGCCC[-/T]TGGACCTCCCTCCAT	146691
rs745836923	snp	A/G	1.65179e-05	0.00287379	synonymous-codon, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17869408	CTCGGTGACCTCCTC[A/G]TTGGACACGCGGGAG	146691
rs745858209	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17964520	ATTTGTGAGGACGCA[A/C]ATTGTGGAGATTTTT	146691
rs745885112	snp	A/C/G	4.94395e-05	0.00497169	missense, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17882757	AGAGCTGGGGCCTGC[A/C/G]GTGCGGAGTAGGGAG	146691
rs745939172	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17880377	CAAGTTGCCCATCAG[C/T]GATCCCAAAGCCTGG	146691
rs745964947	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17959166	ATGGGGAAGGCATCA[C/T]GGGAATCCCCAATTT	146691
rs745994971	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17878718	CAGGTTGCTAAATCA[A/G]TCTGGCTCCTGACCT	146691
rs745996324	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17928545	TTTAACACTCAGCTC[A/G]TTGCCTCCTCTCAGT	146691
rs746028180	snp	C/G			upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	TOM1L2, DRC3	GRCh38.p7	17:17973876	GGATCTGTTATCTGT[C/G]AGGAGGCCACTCCGT	146691
rs746046553	in-del	-/GA			intron-variant	TOM1L2	GRCh38.p7	17:17871348	TGCACTCCAGACTGG[-/GA]GAGAGAGCGAGACTC	146691
rs746047482	snp	A/C/G	6.23466e-05	0.00558302	synonymous-codon, missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17866411	GTCTTCGGTTACTTC[A/C/G]TTCAGTACCTGTCAG	146691
rs746054615	in-del	-/AGG			intron-variant	TOM1L2	GRCh38.p7	17:17953469	CACTTTCCCCACCTC[-/AGG]AGGACAGAGAACCAC	146691
rs746076363	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17927260	TATTTTCAGCACACT[A/G]TACCAAGTCAAGCTG	146691
rs746112680	snp	C/T			intron-variant, downstream-variant-500B	TOM1L2, LOC100507131	GRCh38.p7	17:17857938	AAGTCACTCTTCAGA[C/T]GTGATCCTTTGCCAC	146691
rs746114940	snp	C/T	6.59196e-05	0.00574068	synonymous-codon, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17882819	TGTCCTCTGCTGTGA[C/T]TGGGACCTGGGCATG	146691
rs746130285	snp	G/T	4.04637e-05	0.0044978	intron-variant	TOM1L2	GRCh38.p7	17:17866285	CCCTTTTGTCCCTGT[G/T]AGACACTCACCTAAG	146691
rs746143440	snp	C/T			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17844433	CACCAGGTGGCATGG[C/T]GGGGTGGTGGGGGAA	146691
rs746179627	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17967735	GCCTCAGCCTCCCGA[C/G]TAGCTGGGATTATAC	146691
rs746232571	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17965594	ACAGCGTGACAGGAT[A/G]CCAGCTCTGGAGCCA	146691
rs746252800	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17935783	ATGAAATACAGTTGG[C/T]AAATCAACCTAAAAA	146691
rs746270704	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17902350	CTTTCGGGCAGTTTA[C/T]CAATCTGCACCCACC	146691
rs746278350	snp	A/G	8.27191e-05	0.00643061	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847717	GCAGGAGCCTCCATG[A/G]GGGGCGAGGGGAGGT	146691
rs746286022	in-del	-/GA			intron-variant	TOM1L2	GRCh38.p7	17:17942843	TCGCGACAGCCCTGG[-/GA]GATGGGCCATCACCA	146691
rs746301987	snp	C/T	1.64765e-05	0.00287019	intron-variant	TOM1L2	GRCh38.p7	17:17866859	AGGAGATGACAGGAT[C/T]CTGAAGGAATACTTA	146691
rs746357732	snp	C/T	1.64732e-05	0.0028699	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17898621	AGCATCACCTCTCTG[C/T]AGTTCCGGTTCCCGT	146691
rs746388369	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17850627	TTTTGGAGCCAGCTA[C/T]GGCTAGGACTGTGTG	146691
rs746393977	snp	C/G	1.65157e-05	0.0028736	intron-variant	TOM1L2	GRCh38.p7	17:17847805	TACAAACCAAGGCAA[C/G]GGTCAGGGTTGGTGA	146691
rs746397095	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17901369	GTGTTGAGATGGCAT[C/G]AAGCCCTAGCAGCTT	146691
rs746407239	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17947327	CCGTGCCCAGGCCAG[C/T]GAGCTTTCTGTTTTG	146691
rs746408032	snp	C/G	3.45752e-05	0.00415769	intron-variant	TOM1L2	GRCh38.p7	17:17893852	TCACCCCAGTGGGAG[C/G]TGGAGAAGACACTGG	146691
rs746456339	snp	A/C	1.69392e-05	0.00291021	intron-variant	TOM1L2	GRCh38.p7	17:17893631	TCATCTTACTCTGTT[A/C]CAACAAATTGGGCAA	146691
rs746459280	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17853218	AACTGAAGCTTAGAA[A/T]GTCAGCAGCATCTCC	146691
rs746463373	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17885008	AAAACTTAATTTAGC[A/G]TGTATTTCCTTGGAG	146691
rs746518158	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17943028	ATGCAGAGTGGGAGG[G/T]GAGGATGATTAGATG	146691
rs746520440	in-del	-/A			intron-variant	TOM1L2	GRCh38.p7	17:17899948	GGCATGGTGGCTCAC[-/A]AGTCTGTAATCCCAG	146691
rs746521827	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17956249	TGATTGGTGCGTTTA[C/T]AATCCCTGAGCTAGA	146691
rs746522840	snp	A/G			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847283	AGGGCGGGGCCGGGC[A/G]TGCTCTTTCTCCATG	146691
rs746562460	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17881722	CTAGAGTGAGCAGCA[C/G]AGCTGGGGGCTCACA	146691
rs746566696	snp	C/T	8.7273e-05	0.00660522	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847643	GAGCTGCTCACAGGG[C/T]GAAGAGGGCATCCTC	146691
rs746623439	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17908677	AATGACTAACAAGTA[C/T]GTGAAAAGAGGTTCA	146691
rs746637566	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17923950	AGACCAGCCTGGCCA[A/C]CATGGTGAAACCCCG	146691
rs746642575	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17955779	TTACAGTTCTTAAAG[G/T]CGGCGTGTCTGGGGT	146691
rs746657546	snp	G/T			intron-variant, upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17970987	AGGCAAGTTGCTTTC[G/T]TAGTAAGGAAGTCCC	146691
rs746666657	snp	A/G	1.65677e-05	0.00287812	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17869353	ACCTCTCGTATCGAA[A/G]GAAGACGTTGTTGAG	146691
rs746677069	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17969607	AGTGGGGAGCCATCA[C/T]CATCTTTAGTCAAGC	146691
rs746685451	snp	A/G	0.000115976	0.00761409	intron-variant, synonymous-codon, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17893742	GACCAGAACACTGTC[A/G]ATGAAATCTCGGTTG	146691
rs746711770	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17906184	CCAAAACTGGAGTAC[A/G]GTGGCATGCTCATGG	146691
rs746712401	in-del	-/TTTT			intron-variant	TOM1L2	GRCh38.p7	17:17868901	GAAAAGCTTTTTTTC[-/TTTT]TTCTTTTTTTTTAAG	146691
rs746743519	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17904705	AGCACCTGACCTTGA[C/T]TACCTTTCCAGCCGG	146691
rs746755511	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17919974	TGCCAACCACATGAC[C/T]CAGGTCTTCCTGGTA	146691
rs746771297	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17870251	CCCTCTCTACCCTTA[A/G]AAGCAACATCCCCGT	146691
rs746830043	in-del	ATGGAGTCTCGCTCTGTTG/TGGGGTCT			intron-variant	TOM1L2	GRCh38.p7	17:17920362	TTTTTTTTTTTTGAG[ATGGAGTCTCGCTCTGTTG/TGGGGTCT]CCCAGGCTGGAGTGC	146691
rs746833748	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17964453	CAAGGCATGAGAAGA[C/T]GAAGAGTGAAATACA	146691
rs746836170	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17933512	TGAGGTTCATATTCC[A/C]TTGGGGCCTCTTTCC	146691
rs746859347	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17869013	GGAGCAGGTGCAGAA[A/G]CTCTGGGGCCCAGAG	146691
rs746875894	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17931800	CACTGTTAGCCCCTT[C/G]AGGGTCTCAACACAC	146691
rs746882159	snp	C/T	1.64996e-05	0.0028722	intron-variant	TOM1L2	GRCh38.p7	17:17850985	AGCGGGCCAGGCAGC[C/T]CCCACACAGCCAGCG	146691
rs746887217	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17930710	AATAATTTATACCCA[A/T]GACAAATAAAACAAG	146691
rs746888783	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17963442	AAAAACGCTGGAGCT[A/G]GAGCCCCTGGCTGGA	146691
rs746897087	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17912186	ACACCTCCCAGACGG[G/T]GTGGTGGCCGGGCAG	146691
rs746922305	snp	C/T	1.65825e-05	0.00287941	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17861459	CTCCAGGCAGAAAAA[C/T]AGGGTTAAAGACCTA	146691
rs746931125	in-del	-/A			intron-variant	TOM1L2	GRCh38.p7	17:17930359	CTTGTGAAAGTGGTT[-/A]AAAAAAAAGGGGGGT	146691
rs746942840	snp	A/G	4.94466e-05	0.00497201	missense, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17882830	GTGATTGGGACCTGG[A/G]CATGGTCGCAGCTGG	146691
rs746950450	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17900931	CTGCCACACCCCTCA[A/G]TCCTCTCTTCTGTCC	146691
rs746973884	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17881909	GAGGTTCCACAGTCA[C/T]GACATTGTCGCAAAT	146691
rs746976899	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17856414	ACCTGCCCAGGCTGA[C/G]AGCAGAGCTGTGCAG	146691
rs747000915	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17848046	TTTCCAGATCAGCAC[C/T]GGGTTTTGTCCATTT	146691
rs747024339	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17926985	TATCACACACAGGTT[A/G]TGTAACTTATTAATG	146691
rs747032744	snp	C/T	3.23326e-05	0.00402061	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17866413	CTTCGGTTACTTCAT[C/T]CAGTACCTGTCAGAA	146691
rs747046671	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17877375	TTCCATGGCCTAGCC[A/G]GCACTCTCAGCTCTG	146691
rs747046878	snp	A/G			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17844254	TCTGCGGGGGCCCAG[A/G]GTGGGGTGTGGCAGC	146691
rs747056259	snp	A/G	1.65083e-05	0.00287296	intron-variant	TOM1L2	GRCh38.p7	17:17884595	TGGCTCACCCGTTCT[A/G]CAGTAGGTCTTTCTA	146691
rs747069422	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17939935	GGTGGCTCATGCCTG[C/T]AAATCCTAGCACTCT	146691
rs747076349	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17893976	GCACACGCATTCCCA[C/T]ACTCCATTCTCCAGG	146691
rs747077488	snp	A/G			upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17972583	GAGCTAGGTCACCGG[A/G]GTCCCTGTCAGCCGT	146691
rs747133609	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17892950	AGCCTCCAGCTATAG[C/T]CGAGCCTTCAGACAA	146691
rs747165786	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17856749	CTTTGGGCTCTGCTA[A/G]AGGTGAAATGGTCAT	146691
rs747179993	snp	C/T			intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17862263	AATCAACTCCCTGAA[C/T]TCCAGATGGCTCATC	146691
rs747248724	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17938642	CTCATAAATGCACAG[A/G]GACGCAACCCAGCAG	146691
rs747252656	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17952946	TGAAAAGGTGTATAC[A/G]CATTCTCAAAAGCAG	146691
rs747256499	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17905665	TGCCTCAGCCTCGTA[C/G]AGTGCTGGGATTGCA	146691
rs747260299	in-del	-/T			intron-variant	TOM1L2	GRCh38.p7	17:17849879	ATGTCCCGGGGTGTG[-/T]TCTTCCTCCCTGACA	146691
rs747269852	snp	C/G	3.29478e-05	0.00405867	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17866886	CTTACTCCATTACTG[C/G]CATTTTGAACGGATC	146691
rs747279229	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17876849	CAAGAGGGCTGCTGT[A/G]AACAGCCTGTCACTG	146691
rs747281852	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17901273	AGATAGTGTGGAGTT[A/G]GAAACCAGGAGAAGA	146691
rs747313668	in-del	-/TCC			cds-indel, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17843729	CGACATTCAACACAT[-/TCC]TCTTTTCAGTAGCCC	146691
rs747325600	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17948211	TATCAACCTTTCACT[A/G]AGACTTGCTGTACTG	146691
rs747378720	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17946945	GGCCAGGCTGGTCTC[C/G]AGCTCCTGACCTCAA	146691
rs747386892	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17940732	GTGACCTCGCTAATT[C/T]AAATAAATAGCCACA	146691
rs747415329	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17865972	GTCTCAAACTCCTGA[A/C]CTCAGGTGATCCACC	146691
rs747446015	snp	C/T	1.6492e-05	0.00287154	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17848844	TTGTGACACCCTCCT[C/T]CAGATCATCACCCTT	146691
rs747447159	snp	A/G	1.65228e-05	0.00287422	intron-variant	TOM1L2	GRCh38.p7	17:17879765	GGGGCCACGAGGAAG[A/G]AAAGCAGGAAGGAAA	146691
rs747466004	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17967819	TGCCACATTAACCAG[A/G]CTGGTCTTGAACTCC	146691
rs747474891	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17899782	CTTTCCCAGCTTGCA[C/T]GTTTGTTAAGTCAGG	146691
rs747499154	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17897558	AAACTGTTAGTTCTC[A/G]AGACAGAAATAACAC	146691
rs747500901	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17914222	CACCATTTCACTGCT[A/G]CAGGCTCCCAGCACA	146691
rs747502553	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17863481	GTGTGAAGTGAACAA[C/T]GCTCACAGGAAAAAA	146691
rs747508549	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17957042	AGAGTACAGTGGCAC[A/C]ATCATAGCTCGCTGC	146691
rs747587595	snp	A/T			upstream-variant-2KB, utr-variant-5-prime, intron-variant	TOM1L2, DRC3	GRCh38.p7	17:17973669	AATGGAGACAGGGTC[A/T]TCCTATGTTGCCCGG	146691
rs747599352	snp	C/T	6.6107e-05	0.00574884	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17869434	GGGAGATGAGCTCCA[C/T]GATGCGCTGCTGCAT	146691
rs747601347	snp	A/C	1.71428e-05	0.00292765	intron-variant	TOM1L2	GRCh38.p7	17:17893844	GAAAAGGGTCACCCC[A/C]GTGGGAGCTGGAGAA	146691
rs747646725	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17941609	GTCCCTCACCTGCCC[A/G]TCCCTAAAGGCAGAG	146691
rs747662142	in-del	-/C			intron-variant	TOM1L2	GRCh38.p7	17:17954949	CATCCATTTGCTCAG[-/C]CCCCTTCCTGACCTC	146691
rs747668712	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17954509	GTAGAGACGGGGTTT[C/T]GCCATGTTGGCCAGG	146691
rs747688594	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17969336	GCTGGGATTACAGGC[A/G]TGAGCCACCACAACC	146691
rs747706029	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17872810	TACAAGAAAGTGTGG[C/T]CTCTGGGGCTTGTGG	146691
rs747765487	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17935699	CCTTATTATACCATC[C/T]CTAAAGTCCACCAAT	146691
rs747792852	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17968169	CATGTTACCTCTACC[A/G]AAGGCTCCCTAAGAG	146691
rs747804798	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17851605	TCAACAGAAACACAG[C/T]AAAAACGAGGGCTCT	146691
rs747813834	snp	C/T	4.95937e-05	0.0049794	missense, upstream-variant-2KB, intron-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17861489	ACCCCTTCTGAACTC[C/T]GTTTTCGATTGTCTA	146691
rs747829782	snp	C/T	1.71947e-05	0.00293207	intron-variant	TOM1L2	GRCh38.p7	17:17869519	GCTGGGTGTGCTTTT[C/T]GTCACATTCTATCTC	146691
rs747833234	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17874715	AGGAACATCTGCTCT[A/G]GCCTTGTGTTTGCTG	146691
rs747847465	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17949564	CTGGGGTGAAGACAG[C/T]GGCTCTCTGGTCAGA	146691
rs747879783	in-del	-/CT			intron-variant	TOM1L2	GRCh38.p7	17:17880593	CTACTGGTCCCATCA[-/CT]CAGTGACAAGAGACC	146691
rs747898269	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17917582	GGGAATACATGTGCA[G/T]GCCACCATGCCTGGC	146691
rs747952288	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17908651	AGACATTTCTCCAAA[G/T]AAGATATATAAATGA	146691
rs747971457	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17913373	TGCCAGCCTAGGCTG[G/T]GCTGTGAGCTCCATG	146691
rs747997662	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17896694	TTTTCCAGAATGAAG[C/G]CAAAAGCCATGGAGA	146691
rs747997839	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17880631	CGCTGGACAGAGGTC[A/C]AGAACTGCACAGGAC	146691
rs748001425	snp	C/T	1.64741e-05	0.00286998	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17866901	GCATTTTGAACGGAT[C/T]GGCCAGACCTGTATC	146691
rs748054540	snp	C/T	3.29984e-05	0.00406179	intron-variant	TOM1L2	GRCh38.p7	17:17884609	TGCAGTAGGTCTTTC[C/T]AGAAAGTGCCAGCTG	146691
rs748067352	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17936212	GTTTTCACACATTCT[A/G]TTCTCTCTGCCTGGA	146691
rs748084321	snp	C/G	1.6473e-05	0.00286988	missense, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17884693	TGGGAAATTCAACCC[C/G]TTTCCTCTTCAGCTC	146691
rs748092164	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17906418	ACAGATGTGACCCAC[C/T]GAGCCCAGCCAAGAC	146691
rs748122035	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17890535	TCAACAGTGGGAGGG[A/G]TAAATAAACTGTAGT	146691
rs748137143	snp	A/C			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17845684	CCAAAGGGCTGGGGC[A/C]TCTGGGTGCACCTGG	146691
rs748142911	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17955623	GGATTACAGGCATAA[A/G]CCACTGCGCCCAGCC	146691
rs748163921	in-del	-/AGAGGGAGAGGGAGACCGTGGGGAGACGGG			intron-variant	TOM1L2	GRCh38.p7	17:17913181	GGAGACCGTGGAAAC[lengthTooLong]AGAGGGAGAGGGAGA	146691
rs748189699	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17938379	TCTTAGACCCTTGGT[C/G]CCTTTGATTTCACTG	146691
rs748251469	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17937391	CTGATGAATAACCAG[C/T]CATGATCAATGCCTC	146691
rs748293360	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17904515	TGGAGCTGCCGAGGG[G/T]TCTGGGGCTCCTCAT	146691
rs748294220	snp	C/G	1.65255e-05	0.00287445	intron-variant	TOM1L2	GRCh38.p7	17:17847834	GAGGGCAGGCCACCA[C/G]AGGAAGCGCACCCTT	146691
rs748314928	snp	A/C	6.02391e-05	0.0054878	intron-variant	TOM1L2	GRCh38.p7	17:17869229	ATGAGTATTTTCCAA[A/C]TCTAATCTCTCTCCC	146691
rs748317970	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17964245	GAATGTTATTTATAT[C/T]TTCTCAGACTACTAG	146691
rs748340121	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17927213	ACTGCATTCTTCAAT[A/G]GGGGTGGAGTCCAAA	146691
rs748341857	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17853387	ATTAAGGGGTCAGGG[A/G]CCTTAAACCTTCAGA	146691
rs748348493	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17902785	GTGAAATAGTACATC[A/C]ACATAGATATAGTAT	146691
rs748374050	in-del	-/T			intron-variant	TOM1L2	GRCh38.p7	17:17910044	TTAAAAAACTTTTTG[-/T]TGAATGGTTAAAATG	146691
rs748402080	in-del	-/GAAA	1.65012e-05	0.00287234	intron-variant	TOM1L2	GRCh38.p7	17:17879612	AGGCCAAGTGCTTCT[-/GAAA]GAAAGATGACTCACC	146691
rs748412305	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17945432	TTCTCTGAGAGAACA[C/G]TTATACATCAAAACA	146691
rs748433507	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17868840	CCGGCACTTACACCC[G/T]CCTGCTTCCCCTGAA	146691
rs748456867	snp	C/G	1.65699e-05	0.00287831	intron-variant	TOM1L2	GRCh38.p7	17:17879791	GGAAAGGTCAGTCAG[C/G]CTGCACTTGCAATAT	146691
rs748473076	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17919658	CATGGGGGAGGAGGG[A/G]CCACGGTGTTGTTGC	146691
rs748480864	snp	C/T	3.29462e-05	0.00405857	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17898634	TGTAGTTCCGGTTCC[C/T]GTTGAGCCGCTTCTT	146691
rs748490426	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17863109	ATTGCTGGGGTGACA[A/T]GGCAGGGACTGGCGC	146691
rs748520130	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17956969	AGCCAGAGAAGGCAT[C/T]GGGGCTGAGGAGGCG	146691
rs748578182	snp	C/T			intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17861319	CTCAATGAGGCACTA[C/T]CTGGGTTCCACGGGG	146691
rs748596966	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17876996	GCATAGCTCAAGAGG[A/G]GGAGTTGCTGTGTTC	146691
rs748605305	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17910716	CTGGGATTACAGGCA[C/T]GTGCCACCATGCCTG	146691
rs748630488	snp	C/G	1.65581e-05	0.00287728	intron-variant	TOM1L2	GRCh38.p7	17:17862893	TGAGAACAAAATGTA[C/G]ACTGTAGATCTGATG	146691
rs748636859	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17875801	AACACGGAATAAGGT[A/C]CTGAAGATCTGTTTT	146691
rs748642747	snp	A/G			utr-variant-5-prime, upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17972463	CCCCGCCCCCTTGCC[A/G]CGTCTCTATTGGGGG	146691
rs748681398	snp	A/G	1.64822e-05	0.00287068	missense, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17882736	GTGATGGGGCCAGTC[A/G]CACTCAGAGCTGGGG	146691
rs748695672	snp	C/T			intron-variant, upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17971303	AGGGGAACTTCAAAC[C/T]AGAAAGGGCACAAGG	146691
rs748719552	in-del	-/T	1.66815e-05	0.00288799	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17861585	CACAAGCAGAGTTCA[-/T]TTTCCTCCAGTGGTC	146691
rs748721824	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17892630	CCACCCCAAGCCCTG[C/T]CCCCAACATTCTTCA	146691
rs748739941	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17921853	AGCGCCTCCCAGGGG[C/T]TGTTCCCCTCGCCCT	146691
rs748771416	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17871403	GGCCAAGTGCGGTGC[C/T]TCATGCCTGTAATCC	146691
rs748785968	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17886360	CTCTTGGCCAACACT[C/T]CTTCTGGATTCTGAG	146691
rs748789426	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17939607	TCTAATAGGTCATGA[A/G]TTGATAATTGTTGAA	146691
rs748838950	snp	C/T	1.64895e-05	0.00287132	intron-variant	TOM1L2	GRCh38.p7	17:17884790	TAATAGAAGGCCTGT[C/T]AGGAAGCATTTCTCA	146691
rs748862069	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17932318	TATTTTTTGTAGAGA[C/G]AGAGTCTTGGTACTT	146691
rs748862321	snp	C/T	0.000132229	0.00813001	missense, upstream-variant-2KB, intron-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17861523	CAGAAGCAAGTCCTC[C/T]GACAGCCTGAGGATC	146691
rs748862936	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17966477	AACCAGTAGCATCAG[C/G]ATCACTAGAGAACTT	146691
rs748865481	snp	C/T			intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17862215	AAAACATGTACAGTG[C/T]CTCCCTGAGATGTAG	146691
rs748892599	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17964556	CTTTGCATTTTTTCT[A/G]TATCTTTCATATTTT	146691
rs748919013	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17899709	CGGCTGTGGGCCAGC[A/G]CTTTGCAATCACACA	146691
rs748970792	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17865103	GTATAACCAATGTGC[C/T]AGAGTCATATACACA	146691
rs748982732	snp	A/C	1.66112e-05	0.00288189	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17862706	CCAATATCTTTAGAG[A/C]GCCACTAAAAGGGGC	146691
rs749027579	snp	C/T			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17845369	GCGCTGGAGCTGGAG[C/T]GGGGCAGTTCTGGGA	146691
rs749045062	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17928666	CTCATCCAGCCCCTA[C/T]TGCTTGTCTAATGGT	146691
rs749059907	snp	A/G			upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	TOM1L2, DRC3	GRCh38.p7	17:17973905	GTTGACAGTTGTGTA[A/G]AACTCTGCTGCTTTC	146691
rs749074543	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17894398	TAATGTCCATGTTCA[A/G]TTCAGACCCTGCCTG	146691
rs749089338	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17953443	TAGAGACAAGCAGGA[A/G]TGCCCCGGATCACTT	146691
rs749155020	snp	A/T	1.64993e-05	0.00287218	intron-variant	TOM1L2	GRCh38.p7	17:17848886	GCAGAGAAAATGAAA[A/T]TAGGGCACTGGTCCA	146691
rs749159172	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17922878	AGCCTCCAGGTGGAA[C/T]AGTGAAGTGGCCACC	146691
rs749164024	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17908284	GGACCCTTTATCTTA[C/T]ACCATATACAAAAAT	146691
rs749182631	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17954257	GTAAGAGAAAAGACG[A/G]GAAGAAGCCCAGTCA	146691
rs749235975	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17968045	ATGAACACGCTAAGT[A/G]TTCTACTAAATCGTA	146691
rs749254571	snp	A/T	1.64895e-05	0.00287132	intron-variant	TOM1L2	GRCh38.p7	17:17884789	ATAATAGAAGGCCTG[A/T]TAGGAAGCATTTCTC	146691
rs749254637	snp	C/G	3.5113e-05	0.0041899	intron-variant	TOM1L2	GRCh38.p7	17:17869263	CCCTCTCTTTCCTTT[C/G]TTTATGAAAGAAATC	146691
rs749266578	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17871934	GGGGACACTACTATC[C/T]AGTAAAGAGAAAACT	146691
rs749268375	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17902692	GTGAATCCACCAAGA[C/T]AGTCACCAAGACTGG	146691
rs749282889	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17936149	CTCCACCCTCCCTTC[A/G]GCCTCTGGCCTTAGC	146691
rs749294956	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17868305	CTGGTGTGTACTTCC[A/G]TAGTCAAAAGATGAG	146691
rs749332559	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17851938	GGCTAAAAAGGTTTA[A/G]GTTGCCATCAAATAT	146691
rs749335247	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17949515	GTGCCAGGGTGGGTA[C/T]ATGAAAAAAGTTAAC	146691
rs749386546	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17948594	GAGGTGGAGGTTGCA[C/G]TGAGCTGGGACCATG	146691
rs749424036	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17867289	GGGCTGTGTTCAGGA[C/G]CAACTAGCTAGTGTT	146691
rs749448921	snp	C/T	1.64817e-05	0.00287064	intron-variant	TOM1L2	GRCh38.p7	17:17850888	ATAGAAAAGTCGAGT[C/T]TCACCAGGTCGGTCC	146691
rs749487565	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17902107	CTTGAGCCTGGGAGG[C/T]GGTGGTTGTGGTGAG	146691
rs749491298	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17929364	TGTCAGAGCCTGGGC[A/G]TGGTGGCTCACGCCT	146691
rs749496502	snp	C/T	0.000335965	0.0129565	intron-variant, upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17972230	ATCAGCGGCCGCCGT[C/T]GCCCAGCCTCCTGCC	146691
rs749513155	snp	C/T			upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17972755	AGGAATATCCCCGCC[C/T]ATAGAAAGTACTGAT	146691
rs749543208	snp	A/T	1.66178e-05	0.00288247	intron-variant	TOM1L2	GRCh38.p7	17:17882667	GATGAAAAAGGATAG[A/T]CAGCTGGCTTGCCTA	146691
rs749547547	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17925250	CCTAATACAGCCATT[A/G]TAAGTAATAATTCTT	146691
rs749559586	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17880479	CTGTGCCTCAGATCT[A/G]CCCCTTCACTCCCTC	146691
rs749583525	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17909658	CAGTTTGGGGAAAAT[A/G]AAAGAGTTCTGGAGA	146691
rs749600116	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17889209	GGCAGCCAGAAGACA[A/G]AAAGCCCCCATACGG	146691
rs749661601	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17875574	GCTTTGGCCTTCTCC[A/C]ATTTCTGGTCCTCAA	146691
rs749674386	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17938154	ACTACAGGTAGAAAT[C/G]AGAGGGAGGCAGTTA	146691
rs749714960	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17874333	TGGAGTACGGTGGTA[C/G]GATCTCAGCTCACTG	146691
rs749717710	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17924091	GCAGTGAGCCGAGAT[C/T]GCGCCACTGCACTCC	146691
rs749725555	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17919914	AGAAAATGAAGCCTG[C/G]TGGGGTGACTAGCCC	146691
rs749736892	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17970036	TATCTCTTATATTTG[G/T]TTTTTTGTTGTTGTT	146691
rs749737963	in-del	-/AATATT			intron-variant	TOM1L2	GRCh38.p7	17:17867872	TACAAGGAGAACAGG[-/AATATT]AATACATCTGAAACA	146691
rs749744673	snp	A/G	1.65583e-05	0.00287731	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847714	GGGGCAGGAGCCTCC[A/G]TGGGGGGCGAGGGGA	146691
rs749767014	in-del	-/A	1.64959e-05	0.00287188	intron-variant	TOM1L2	GRCh38.p7	17:17884611	AGTAGGTCTTTCTAG[-/A]AAAGTGCCAGCTGGA	146691
rs749774885	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17937207	CTATTCAACATGAAC[C/G]CTTCCTCCCACAGAA	146691
rs749797892	snp	A/G	3.43855e-05	0.00414627	synonymous-codon, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847647	TGCTCACAGGGCGAA[A/G]AGGGCATCCTCTGAC	146691
rs749804679	snp	A/G	3.31549e-05	0.0040714	intron-variant, missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17893761	AAATCTCGGTTGGCC[A/G]CAAGGATGTGGAAGC	146691
rs749826095	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17904251	ACTTGAAGAGAAAGA[C/T]GTGTGTGACCAGCCT	146691
rs749841438	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17888600	GCTACCAGGCTCTGA[C/T]GTCTTCAAAGAACAC	146691
rs749865300	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17946512	AACATAATATTTTTA[C/T]CCAATTCTATTTTTT	146691
rs749913395	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17960239	ATACTAAGCTCTCTG[A/G]TTTAGTGGTTAAGAG	146691
rs749916322	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17958217	AACGAACAAACCATG[A/C]TCTTCAAATGAGTAA	146691
rs749992298	snp	C/T	2.1339e-05	0.00326635	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17866344	GGGGCGCTGTGTTCC[C/T]CACCATTGGGCTCAC	146691
rs750044741	in-del	-/T			intron-variant, upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17970871	GGCTCATAAAAGACG[-/T]TTTACCAGTCCTTCA	146691
rs750068888	in-del	-/G			intron-variant	TOM1L2	GRCh38.p7	17:17947771	GAGGTTACTGGAGCT[-/G]GGACTCAAAGTGAAG	146691
rs750097221	snp	C/T	1.65037e-05	0.00287256	intron-variant	TOM1L2	GRCh38.p7	17:17862858	CCAAGTCTGTGGCAA[C/T]AAAACAAATGGGTGG	146691
rs750109036	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17876805	GCTGTGCTGCTGCCC[A/G]AAGTCTAACCAAGAT	146691
rs750116499	in-del	-/A			intron-variant	TOM1L2	GRCh38.p7	17:17933422	AATCCAAACAAAATC[-/A]AGACTCCGTCAGAAA	146691
rs750125189	snp	C/T			utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	TOM1L2, DRC3	GRCh38.p7	17:17972370	CACCTAGGCCTCCGC[C/T]GTAACCCGCCGGACT	146691
rs750130496	snp	C/T	3.31307e-05	0.00406992	intron-variant, missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17893720	TGTTCTTGGGAGATA[C/T]AATTTTGACCAGAAC	146691
rs750178998	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17886880	GGGCCAATCAGATGC[C/T]CCTCCTTCCAGGAAC	146691
rs750185610	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17887425	TTCATATGTGAAAAC[A/G]TACAGATGGGAGACA	146691
rs750191506	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17960625	TTACAGGCATGAGCC[A/T]GTGAGCCCAGCTGGT	146691
rs750220704	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17884862	TCTCCCCGAGACCAG[C/T]GCTCTCCTACTTGCA	146691
rs750224529	snp	C/T	1.6585e-05	0.00287962	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847697	CAGAAGGGTTTGAGG[C/T]TGGGGCAGGAGCCTC	146691
rs750238318	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17967972	AATAAAGGGCGGGAT[A/G]GATGCAAGAAATGCA	146691
rs750285479	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17885847	GGAGAATGGTGTGAA[C/T]CCGGGAGGCAGAGCT	146691
rs750311763	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17934702	GAAATAACAATATGC[A/G]ATATTTCATCTTATC	146691
rs750334449	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17851200	GCCGGCGGTAAGGAA[A/G]GTGGCTGTACGCGTT	146691
rs750339716	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17947313	ATAGACATGAGCCAC[C/T]GTGCCCAGGCCAGTG	146691
rs750341953	snp	C/T	1.66358e-05	0.00288402	intron-variant	TOM1L2	GRCh38.p7	17:17869482	TGAGCTCCTAGGGAA[C/T]ACATGCACCTCTGGG	146691
rs750353103	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17947915	TATTTTTTTTTAAAT[A/G]TATACTCTTTCCAGA	146691
rs750364926	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17933614	CATCATTTTGAGGGC[C/T]ACCACCACACTTACA	146691
rs750372060	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17849920	TGCCTTCTTTGGCAA[C/G]GCATGTGTTTGGAAA	146691
rs750393007	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17900789	AATATGGGACTTAAC[C/G]GGCTCTCTGCTTTGA	146691
rs750398681	in-del	-/CC			intron-variant	TOM1L2	GRCh38.p7	17:17848079	AGATCAGCACTGGGG[-/CC]GTGGGGCAGGGTAAG	146691
rs750408389	snp	A/T	1.6836e-05	0.00290133	intron-variant	TOM1L2	GRCh38.p7	17:17893814	TGTCTCCAGCACCTG[A/T]TGTGGGGAGGGAAGG	146691
rs750422363	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17922379	AGTCTGGGCTTTCCA[C/T]AGGAGGCAACATGGG	146691
rs750461122	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17915308	ATGCAAACATCCAGG[C/T]TTTAGAGACAGAACT	146691
rs750514553	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17895281	ATGCCTCCTCAAAAC[A/G]ATGTCACCAGCAACA	146691
rs750563948	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17942298	CATTAATAAATAGCA[A/G]TAATAAGGATGGGGG	146691
rs750569886	snp	A/G	1.6638e-05	0.00288422	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17861442	ACTTTCCCTCCAGAA[A/G]ACTCCAGGCAGAAAA	146691
rs750570366	snp	A/C	1.64991e-05	0.00287215	intron-variant	TOM1L2	GRCh38.p7	17:17879615	GCCAAGTGCTTCTGA[A/C]AGATGACTCACCTGC	146691
rs750589862	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17938147	ACCCAGGACTACAGG[C/T]AGAAATGAGAGGGAG	146691
rs750626922	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17873551	AGAACCAAACCAGAT[C/T]CCTCAGTAGACTGCA	146691
rs750638324	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17908150	GGTGTTGGGTGTTTC[A/G]CGTACATTATTTTAT	146691
rs750642205	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17907973	ATGAAAATTAAATGG[A/G]TTGATATACATGAAA	146691
rs750644729	snp	C/T	8.26166e-05	0.00642662	intron-variant	TOM1L2	GRCh38.p7	17:17884589	GCAGCTTGGCTCACC[C/T]GTTCTGCAGTAGGTC	146691
rs750659543	snp	C/G	5.0176e-05	0.00500854	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17861592	AGAGTTCATTTTCCT[C/G]CAGTGGTCATGGAGG	146691
rs750778180	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17869721	TATGTATACAAGTAC[A/G]TGCTTGTACAAATCA	146691
rs750786670	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17919551	CACAATTTCCTTAAG[A/C]ATCCAAGCATTAAAA	146691
rs750845304	in-del	-/A			intron-variant	TOM1L2	GRCh38.p7	17:17877878	CTGATGGGCTTGTTT[-/A]AAAAAAAAAAAAAAT	146691
rs750846831	snp	A/C/G	4.95232e-05	0.0049759	intron-variant	TOM1L2	GRCh38.p7	17:17848808	GGGGCTGTAAGGCCA[A/C/G]TGGCCAGGCCATACC	146691
rs750897013	snp	A/C	1.6661e-05	0.00288621	intron-variant	TOM1L2	GRCh38.p7	17:17869327	AAAAAAAAAAAAGAA[A/C]TCCGGCTCCCACCTC	146691
rs750919459	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17954710	GTGTAGAAAGGGAGG[A/G]AGAATATGAAGGAGG	146691
rs750931556	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17848390	GCAGGGGATGTGGGG[G/T]TGGCCATGTGGGAGA	146691
rs750938085	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17881279	GCTATGGGCAGCCAC[A/C]CAGTAGACTCTGAAG	146691
rs750960868	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17962765	AGAGATCGAGACCAA[C/G]CTGGCCAACATGGTG	146691
rs750983349	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17956776	TGCGGTGCTGGGCCC[G/T]CTGAGCTCACGCCCA	146691
rs750995209	in-del	-/TT			intron-variant	TOM1L2	GRCh38.p7	17:17875937	CTTGGCCGTTCTGTC[-/TT]TGTTGAAATGAGACG	146691
rs750999644	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17876593	TCTAACAATAGTCAC[A/G]AAAGCTAGGATTTGT	146691
rs751008531	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17921962	ACCAGCCTTTTTTTT[G/T]AGCTTCTCCCGATGA	146691
rs751043539	snp	A/G			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17843891	CTATGGCTGGTGGCC[A/G]CAGGGGAAGCCTGAC	146691
rs751084535	snp	A/G			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17845184	GGGCAGGCTACCTCC[A/G]GATAGGAGGTGCAAG	146691
rs751100466	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17939235	ACGAATACCAGGCAA[A/G]AAGTTGGCAGCTGGC	146691
rs751128344	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17947626	TGAGAAAATAAGTTC[A/G]GTTAAGCCTTCCAGT	146691
rs751129069	snp	C/G	1.65225e-05	0.00287419	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847736	GCGAGGGGAGGTCGG[C/G]AACCATTTCAGCAGC	146691
rs751132404	snp	C/T	4.70389e-05	0.00484946	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17866362	CCATTGGGCTCACCA[C/T]GGCTGGAGACCCTGG	146691
rs751134122	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17925026	CACTCCCTCCTCCAC[A/T]CTCTCTCTCTGTTTT	146691
rs751134511	snp	C/T	1.65924e-05	0.00288027	intron-variant	TOM1L2	GRCh38.p7	17:17882885	TGGCAACAACAAAGT[C/T]CTCTGTTTACCTGGG	146691
rs751136885	snp	C/T			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17843831	GAGAGCCTGGAGGTA[C/T]GGACAGACAGAAGCA	146691
rs751164339	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17873492	CACAGCAGAAGCCCC[A/G]AAACAAAGAGTAGGC	146691
rs751183454	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17945012	CCGCCACACTAATCC[C/T]TCATCCTCCGGGGCC	146691
rs751205487	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17892304	TCCTGCATTCTCCGC[A/T]GCCTCTGCCTGGTTG	146691
rs751221794	snp	A/G	3.38495e-05	0.00411383	intron-variant	TOM1L2	GRCh38.p7	17:17893823	CACCTGATGTGGGGA[A/G]GGAAGGAAAAGGGTC	146691
rs751226171	snp	A/G	1.648e-05	0.0028705	intron-variant	TOM1L2	GRCh38.p7	17:17866839	GGAGGGGTAGGTCTG[A/G]CCTCAGGAGATGACA	146691
rs751237099	snp	A/G	1.65707e-05	0.00287838	synonymous-codon, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847704	GTTTGAGGCTGGGGC[A/G]GGAGCCTCCATGGGG	146691
rs751260400	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17905096	AGCCACTCGGAGCCC[A/G]GTGACGATGGGATTA	146691
rs751272575	in-del	-/GA			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847416	CCCATGGTGGGAGGG[-/GA]GAGAGTCTCTGGCTG	146691
rs751331021	in-del	-/CT			intron-variant	TOM1L2	GRCh38.p7	17:17935884	AATTCTGAGGAATGA[-/CT]CACACTGGTGGTGCC	146691
rs751336157	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17933188	GCCTGAGGCTTCCCT[A/C]CTTTCCATCCTTCCA	146691
rs751340525	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17849843	GAAGCAATTTCTTTT[C/T]GAGACAGCCCCTTGG	146691
rs751345435	snp	G/T			intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17860998	AGGCCAGTGACAAAT[G/T]GCCATCAGAGATGTG	146691
rs751366095	snp	C/T	1.67562e-05	0.00289444	intron-variant	TOM1L2	GRCh38.p7	17:17869494	GAACACATGCACCTC[C/T]GGGTAGCCTGCTGGG	146691
rs751412899	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17891698	CCTAACATGAATTCC[C/T]GGGGGTATTGAGGTA	146691
rs751419089	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17899442	AGTTCACAAATGGGC[C/T]CTGTCCAAAAGTTGG	146691
rs751443530	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17863920	TGCCCAAGCTGGAGT[A/G]CAGTGGCATGATCTC	146691
rs751454637	snp	A/T	1.6476e-05	0.00287014	intron-variant	TOM1L2	GRCh38.p7	17:17898586	TCTCCTCAAGGAGAA[A/T]AGCACTCACTGTTAA	146691
rs751460739	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17946438	TGTGTCTATTCTGAA[C/G]ATTTCTTATAAATGC	146691
rs751484434	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17958195	CCTCTGTTCTTCAAA[A/G]CAAACGAACGAACAA	146691
rs751507886	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17944958	GCAATTCCCAACACC[A/G]TACTCCTGACATTGC	146691
rs751515077	snp	C/T	4.94743e-05	0.0049734	synonymous-codon, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17879633	ATGACTCACCTGCAG[C/T]AACTCCAGATCAGAT	146691
rs751526505	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17911196	CTGGCCTGGGTCCTA[C/T]CCCAGGCGAGAGAAA	146691
rs751533252	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17877931	AACACGAAGTATTCC[C/T]GCTGTCTGGGTCTGC	146691
rs751564934	in-del	-/A			intron-variant	TOM1L2	GRCh38.p7	17:17948675	AGGTGGCCCTTTCTT[-/A]AGAGTGAAAGCAGCC	146691
rs751577933	in-del	-/C			intron-variant	TOM1L2	GRCh38.p7	17:17937287	GCATTCTACTGTAAT[-/C]CTATTCAAGGAACAC	146691
rs751615684	snp	A/G/T			intron-variant	TOM1L2	GRCh38.p7	17:17941028	AGTGTTTTCTTAGGG[A/G/T]AAACTACACTTCTGA	146691
rs751628213	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17906691	TGAAAGCAGGACCAA[G/T]CTTGAGAGGCTGGTC	146691
rs751630579	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17880433	CTCCAGCAACAGAGA[C/T]ATCATACACTTTCTC	146691
rs751640416	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17907852	CAAACTACCTAGGTT[C/T]AAATACAGGCTCCAC	146691
rs751672657	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17953842	TGAAAGAACACAGCA[C/T]AGTCCCCTGCACAAG	146691
rs751678159	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17857649	TGCCAGAAAGAAAGC[A/G]TGTGGCCTTGTACTG	146691
rs751704990	in-del	-/G			intron-variant	TOM1L2	GRCh38.p7	17:17866458	AAGCCCCAGAACCCT[-/G]GGAGTCAGGCTCTGA	146691
rs751763566	snp	C/T	1.6473e-05	0.00286988	missense, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17884687	CTGCCATGGGAAATT[C/T]AACCCCTTTCCTCTT	146691
rs751768019	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17872168	GGGAAACACTCATTA[C/T]AGAATGAAGCATACT	146691
rs751774414	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17967676	CAAATGGCACGATCT[C/T]GGCTCACTGCAACCT	146691
rs751871997	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17960808	AAACTACATAACCCA[A/G]TACCTAGTAAGGAGA	146691
rs751939469	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17931564	ATCTGTCTTCTCTCC[C/T]CCTCCCCCGTACAAA	146691
rs751964140	snp	A/G			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17846264	GTGCATGCTGGAGGG[A/G]ACAGGAGCAGACTGA	146691
rs751984670	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17942047	TGAATGTTCTGTTCT[C/T]TCTACTTCTCTCCAT	146691
rs752009757	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17896212	ACAGGCACCCTTCTC[C/T]CTAGGATTCTCTAAA	146691
rs752065415	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17894822	TGTAATCCCAGCTAC[C/T]TGGGAGGCTGAGGCA	146691
rs752085780	snp	C/T	1.64727e-05	0.00286986	intron-variant	TOM1L2	GRCh38.p7	17:17907423	AGCTCAGAGAGGCTT[C/T]CCAGGAGAGGGGGGC	146691
rs752132587	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17937755	CTAAATAATGCAGAG[A/G]TGAACACCACTCATG	146691
rs752144027	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17889688	TCGATCTACTTTTCC[A/G]TAATGGAAAGGTTAA	146691
rs752155751	snp	C/T			intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17858690	TGGGTTCAAGCAATT[C/T]GCCTGCCTCAGCCTC	146691
rs752170901	in-del	-/A/AA/GA			intron-variant	TOM1L2	GRCh38.p7	17:17869308	CAATCTTTTCAAGGG[-/A/AA/GA]AAAAAAAAAAAAAAA	146691
rs752171882	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17892606	TGGTCCCATCTCCTG[C/T]CTGCTCCCCCACCCC	146691
rs752191956	in-del	-/AAAAAAAAAAAA			intron-variant	TOM1L2	GRCh38.p7	17:17852865	ACTGAAACTCTGTCT[-/AAAAAAAAAAAA]AAAAAAAAAAAAAAG	146691
rs752259631	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17936902	ATTTTCAGGGGAAAA[A/C]GGCTTTTTAACAGTC	146691
rs752268766	snp	A/G	1.65732e-05	0.00287859	intron-variant	TOM1L2	GRCh38.p7	17:17898710	ATAAAGATACTTACA[A/G]TCCCACTTGAGGACA	146691
rs752273917	snp	A/G	1.65135e-05	0.00287341	synonymous-codon, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847755	CATTTCAGCAGCTTT[A/G]GCTCTTTCTTCAAGG	146691
rs752299702	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17888089	CTGAGGGTGGGGGAG[A/G]CTGCCCCCTCTTAAA	146691
rs752320229	snp	A/G	6.59055e-05	0.00574007	intron-variant	TOM1L2	GRCh38.p7	17:17866932	GTTCGAACCTAACAG[A/G]GGAAGGGAAAGCAGA	146691
rs752369407	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17950653	AGAATCTTGCTTTGA[C/T]TTCAATGTATTTATT	146691
rs752374687	snp	A/C	1.64901e-05	0.00287137	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17879661	GATGAATCCTCCTGT[A/C]CAGGGACCATTTCTG	146691
rs752391241	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17944812	ATATTAAATGCTTAG[A/C]GACAAGGCCTAACAG	146691
rs752417986	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17911031	TCAAAGTGTAGAAAG[C/T]GGCAGCCAAAAAGCC	146691
rs752422631	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17902226	AGGTTATTCAGTCAG[C/G]CACTCCTGGTTAATG	146691
rs752425451	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17918126	AGTGTAAATGGAATT[A/G]TTTTCTTTTCTTTTC	146691
rs752427521	snp	C/G/T	6.58951e-05	0.00573969	synonymous-codon, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17898602	AGCACTCACTGTTAA[C/G/T]GCCAGCATCACCTCT	146691
rs752429874	snp	A/G			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17845937	ACCTGAGCAACTGGA[A/G]TGAGACATCCCAGCT	146691
rs752478002	snp	A/G			intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17862544	GTGTTTGGGGGGGTG[A/G]GGGAGGAGGTGGGCA	146691
rs752549363	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17943936	TGCACATCCCTCCCC[A/C]TCCAGGTAAACTCCT	146691
rs752566122	snp	C/T			intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17860509	TGGAAACCAGCACTG[C/T]TGCCTGCCTGGGCCC	146691
rs752600188	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17969110	CGCCCAGGCTGGAGC[A/G]CGGTGGCACAATCTT	146691
rs752605260	snp	A/G	9.90181e-05	0.00703557	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17879731	CGTCCAGTTCACTCC[A/G]CAGCCTGGCAATCTG	146691
rs752635695	snp	A/G			intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17861343	CACGGGGTGTCCCCC[A/G]TGGGTCTCTCCCCCA	146691
rs752635967	snp	C/G	1.64825e-05	0.00287071	missense, intron-variant	TOM1L2	GRCh38.p7	17:17862835	GGTGCCACTGACGCT[C/G]TCTGTCCCCAAGTCT	146691
rs752639009	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17876420	GCCACATTTGTTCCA[C/T]GTGGAGACTGTGCAG	146691
rs752641018	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17927367	AAACCACATGAGGCC[A/G]GCTGCAGAGGCTGTG	146691
rs752662182	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17895761	GAGTGCCTCAGATGA[A/C]AGGCAACATGTGTTA	146691
rs752667466	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17967434	GACACAATGGACCTG[A/C]CTTGGGGAACTCCCC	146691
rs752673044	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17956146	CTACTGCCTCTGGCC[C/T]CACCCACATCCTGCT	146691
rs752674777	snp	A/C			intron-variant, upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17971952	CGGCGAAGGCCCAGC[A/C]CCCCCGGGAGGTGGC	146691
rs752692473	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17891397	GCTGGAAAGTGTGGA[A/G]GGGTGATCCTGATAG	146691
rs752704927	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17931853	AAGATCCTCTTCCTT[A/G]TCAGAAAATAATTCT	146691
rs752719650	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17905603	GAATGCAGTGACACC[A/G]TCCTGGTTCATCACA	146691
rs752763407	snp	C/T	1.87408e-05	0.00306105	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847592	GGTGTCCACGGGGTG[C/T]GAGCGGGGACCCGCC	146691
rs752772057	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17952225	AAACAAAAGCGAGCT[A/G]TAAAATGAAGCCTAC	146691
rs752775745	snp	A/G	1.6483e-05	0.00287076	intron-variant	TOM1L2	GRCh38.p7	17:17884779	CATGCCTGGGATAAT[A/G]GAAGGCCTGTTAGGA	146691
rs752779917	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17855361	GGTTTTGGCAGCAGC[A/G]TTCTTTACTAACCTA	146691
rs752794342	snp	G/T			intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17858250	TTCTCTTTTCTAGTG[G/T]CATGTGTATTCTTTT	146691
rs752823043	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17965900	CCAAGGTGGGTGGAT[C/G]ATCTGAGGTCAGGAG	146691
rs752865783	snp	A/C	0.000200501	0.0100105	splice-donor-variant	TOM1L2	GRCh38.p7	17:17869338	AGAAATCCGGCTCCC[A/C]CCTCTCGTATCGAAG	146691
rs752914306	snp	A/C/T	3.29626e-05	0.00405961	intron-variant	TOM1L2	GRCh38.p7	17:17850883	ATGAAATAGAAAAGT[A/C/T]GAGTCTCACCAGGTC	146691
rs752915063	snp	C/T	1.65291e-05	0.00287476	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17869382	AGGTCATCGTTCACA[C/T]GCAGCAGCTCCTCGG	146691
rs752918202	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17884112	CTAAAGGGACCTTCC[C/T]AGGGCTTTGATCCCA	146691
rs752937756	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17946293	CACAGAGTTGTGCAA[C/T]CATCACCACTATGTA	146691
rs752960667	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17848718	CAGGGCCTGGCACCA[A/G]TAGGTGCTCTGGCAG	146691
rs752966416	snp	C/G	1.65715e-05	0.00287845	intron-variant, synonymous-codon, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17893694	TTTGTCCTGTACAAT[C/G]GTGGGAGGGTTGTTC	146691
rs752973448	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17882608	GTCCCTAACACCCAG[C/T]ACAATACCTGGCTTG	146691
rs752988335	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17874081	CTGCCTCAGCCTTCC[A/G]AGTAGCTGGGATTAC	146691
rs753000513	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17878260	TGGGCTGATGCAGGT[G/T]TGTCAGGAGTGAGGT	146691
rs753012496	snp	C/T			upstream-variant-2KB, intron-variant	TOM1L2, DRC3	GRCh38.p7	17:17973353	TATCAAATGATTTCA[C/T]CTTGGTACTGTATAT	146691
rs753013706	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17958491	ATAAAATGTATTTAC[C/G]TTCATGAGGCTGAGT	146691
rs753042741	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17928026	AAAAATAATCCAGGA[C/T]AAAAGTGTGTGGGGC	146691
rs753053728	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17893534	TTGAAGTATTTTGCA[C/G]CAAATATTTTAAATG	146691
rs753077279	snp	A/G			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17844967	GCTGGTGGGCCTTGA[A/G]AGTCCAGGTTTCCTG	146691
rs753103138	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17894764	GGCGAAGCCCTGCGT[C/G]TACTACAAATACAAA	146691
rs753104834	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17857485	ACTGCTCGGAGCTCC[A/G]GAGACAGTAAAAGGA	146691
rs753110590	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17953676	CCCACCAGCCCAACA[C/T]ACATGAAGACACATG	146691
rs753111994	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17907784	GGCCTAAGCCATCAA[A/C]AATCACCCCAAACAT	146691
rs753148964	snp	A/G	0.000115396	0.00759505	synonymous-codon, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17850950	TGGCTGCGCAACGGG[A/G]ATCTATGGAGGCGGC	146691
rs753169663	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17940801	ATAAGGATTCTGGAT[C/T]ACAGCCCAAAGCTTT	146691
rs753221982	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17935873	TCAATTTAGCAAATT[C/T]TGAGGAATGACTCAC	146691
rs753224690	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17939686	TGTTTAAAATTTTCT[A/G]TAACACAAAGTTTAA	146691
rs753236656	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17906487	CCTCCTCTCTCCCCA[A/T]CTCCCTTCCACAGTC	146691
rs753243638	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17969718	ATCCTCTCCAGATAG[A/G]AAATCCAACCCTAAC	146691
rs753245889	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17935510	AGACCTTGAGCTTGC[C/T]GAGCTGTGCTTTCCA	146691
rs753297574	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17856532	TGGTCACGCTTTGCT[C/G]AAGCAGGTGGACCCT	146691
rs753332131	snp	A/C	3.3465e-05	0.0040904	intron-variant	TOM1L2	GRCh38.p7	17:17898724	AATCCCACTTGAGGA[A/C]ACGATCCTACAGATA	146691
rs753397726	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17967478	AACTCCAAGCAGTTG[G/T]GGAAGGCTGAGATTA	146691
rs753411232	snp	C/T	0.000148384	0.0086122	missense, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17882715	AGTACCTGTTCTGAA[C/T]TGGCTGTGATGGGGC	146691
rs753428300	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17901171	CAAAAGCAAGTATTT[A/C]TCTCTCTCCCCGGGG	146691
rs753430176	snp	C/G	1.64844e-05	0.00287087	intron-variant	TOM1L2	GRCh38.p7	17:17850863	TGCCGCTCCACACCC[C/G]ACAGATGAAATAGAA	146691
rs753460185	in-del	-/TTT			intron-variant	TOM1L2	GRCh38.p7	17:17920218	TTTATTCTCTCGTTC[-/TTT]TTTTTTTTAATTAAT	146691
rs753482261	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17960558	GCCCAGACTGGTCTC[A/G]AACTCCTGAGCTCAA	146691
rs753521545	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17924295	GATTGCTAATGGGTA[C/T]GGAATGATGAAAATG	146691
rs753540800	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17879817	AATATCAGAATCAGC[C/T]TGCTCCTAGTCTAGT	146691
rs753560204	snp	A/C	1.65053e-05	0.0028727	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17879740	CACTCCGCAGCCTGG[A/C]AATCTGGTGGGGGCC	146691
rs753565372	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17929043	GGTTCCTAATACCAA[A/G]TCTGAAGATTCCCCA	146691
rs753572206	snp	C/T			upstream-variant-2KB, intron-variant	TOM1L2, DRC3	GRCh38.p7	17:17974251	TTAAGTTTCTAGAAA[C/T]TTCTCCCATCTACAT	146691
rs753599438	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17875022	AGCACTTTGAGAGGC[C/T]GAGGTTGGTGGATCA	146691
rs753628789	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17880776	GAGTTTCCCATGCGG[C/T]GCCTGGCATGCAGGT	146691
rs753661029	snp	G/T			intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17859136	GGCCCGAGTGCAATG[G/T]CATGATGTCGGCTCA	146691
rs753703432	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17970504	CCTCCATTAACTGGC[C/T]GGAAATTAGTTTTTG	146691
rs753728813	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17944632	ACCAGGCACCTGCTT[C/T]TCTTGTGAAAATCTA	146691
rs753745234	snp	A/G	1.65669e-05	0.00287805	intron-variant, synonymous-codon, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17893703	TACAATGGTGGGAGG[A/G]TTGTTCTTGGGAGAT	146691
rs753756874	snp	C/T	4.9458e-05	0.00497258	missense, intron-variant	TOM1L2	GRCh38.p7	17:17862843	TGACGCTCTCTGTCC[C/T]CAAGTCTGTGGCAAC	146691
rs753780207	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17887628	CTATAAGCATGTGCC[A/C]CCATACCTGGCTAAT	146691
rs753790766	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17936730	TATTAAGTGGGAAAA[A/C]CAGGGCACAAAATTG	146691
rs753811600	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17969227	ACACCCGGCTCATTT[C/T]TGTATTACTAGTAGA	146691
rs753843178	snp	C/T	7.33595e-05	0.00605594	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847604	GTGCGAGCGGGGACC[C/T]GCCATCTGGGGAGGC	146691
rs753847623	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17931439	CTAACCAAATAACTA[A/G]ATGTCTCTGAGCCTC	146691
rs753897149	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17918641	CCAGCCTATCTGCCC[A/G]TATCTAGCTCCCATC	146691
rs753900991	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17948791	CAGAGCAAGGCAGGG[A/G]TCCTAGGAAGGGCTT	146691
rs753967157	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17848475	CTCCCTTCTGGCTCA[A/G]TGGCCCAAGGGTGCT	146691
rs753978800	snp	A/G	1.67683e-05	0.00289549	intron-variant, synonymous-codon, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17893807	TCACACATGTCTCCA[A/G]CACCTGATGTGGGGA	146691
rs753983877	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17962758	AAGGTCAAGAGATCG[A/G]GACCAACCTGGCCAA	146691
rs753985012	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17935877	TTTAGCAAATTCTGA[C/G]GAATGACTCACACTG	146691
rs753985339	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17930378	AAAAAGGGGGGTCTG[C/G]GAATGTGTAGGACCT	146691
rs754015131	snp	A/G	3.29804e-05	0.00406068	intron-variant	TOM1L2	GRCh38.p7	17:17850961	CGGGGATCTATGGAG[A/G]CGGCAAGCAGCGGGC	146691
rs754020024	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17897777	CTGGGTAAACCTCCA[A/G]ACCTCTCTGAGCCTC	146691
rs754045651	snp	A/G	0.000183942	0.00958838	intron-variant, downstream-variant-500B	TOM1L2, LOC100507131	GRCh38.p7	17:17857869	GTCTCAGAAAGAAAA[A/G]TCACAGCAAGACCCA	146691
rs754056131	snp	C/T			intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17860399	TTCTGCGCCCTCTGG[C/T]GACCAGTGCAGAGGG	146691
rs754065157	snp	G/T	0.000132611	0.00814173	synonymous-codon, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17869468	CCGACAGGTCCTGTT[G/T]AGCTCCTAGGGAACA	146691
rs754084671	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17924586	CCAGCCTGAGCAACA[A/T]AAACCTTGCCTCTAC	146691
rs754125495	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17848213	GGGGGGAGTGCCCCA[C/T]TTCTATGGGCACTGA	146691
rs754130490	in-del	-/T			intron-variant	TOM1L2	GRCh38.p7	17:17887832	GTACAGAGAAGGCAG[-/T]CAGTCAACATTTATC	146691
rs754142091	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17892513	TCCCAGCTCAGAGCC[C/T]TTCGATGTCTTCCCA	146691
rs754186084	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17856426	TGACAGCAGAGCTGT[A/G]CAGAGGGCACCAGCC	146691
rs754197006	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17905280	CCTGTGCAGTTCCCT[G/T]TCACATCTTCCAGGA	146691
rs754305360	snp	C/T	1.67349e-05	0.0028926	intron-variant	TOM1L2	GRCh38.p7	17:17882910	CCTGGGCTGCCTGCA[C/T]AGCTGGACCTGGTAC	146691
rs754324486	in-del	-/C			intron-variant	TOM1L2	GRCh38.p7	17:17873445	TACAAAAACCTCCAG[-/C]CAAGGGGTGACCAGC	146691
rs754365679	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17919659	ATGGGGGAGGAGGGG[A/C]CACGGTGTTGTTGCA	146691
rs754367558	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17965661	GCTGTGTGACCTTAG[A/G]TAGGTTCCATACTTT	146691
rs754389023	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17869841	CCTCATTCCTTTCTG[C/T]GTGTTTCATAATGTA	146691
rs754417052	snp	C/T	1.64795e-05	0.00287045	intron-variant	TOM1L2	GRCh38.p7	17:17866840	GAGGGGTAGGTCTGG[C/T]CTCAGGAGATGACAG	146691
rs754447428	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17887705	GGTCTTGAACTCCTG[A/G]ACTCAAGGGATTCAC	146691
rs754460667	in-del	-/ACAT/ACATACAT			intron-variant	TOM1L2	GRCh38.p7	17:17894934	AACTCTGTCTCAAAA[-/ACAT/ACATACAT]ACATACATACATACA	146691
rs754470814	in-del	-/ATT			intron-variant	TOM1L2	GRCh38.p7	17:17903991	TTCACTCAGGAAGAG[-/ATT]ATTATTATTATTATT	146691
rs754498566	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17886407	GCCTCACAGAGCACT[A/G]TCTGGAAGGCCCAGC	146691
rs754514174	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17922131	ACTGAAAGCACTCCC[C/T]AGGAAAGACCTGCAG	146691
rs754532596	in-del	-/ACA			intron-variant	TOM1L2	GRCh38.p7	17:17947821	TTCTTTCCAGAAAGT[-/ACA]ACAAGTTGTATTCAT	146691
rs754533449	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17902048	GGGCGTGGTGGTACA[C/T]ACCTATAATCCCAGC	146691
rs754537760	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17935629	CCCAGGGACCCAGGG[A/C]AAGTCACCTCCTCCC	146691
rs754556673	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17948094	GAGGAAACTAAGGCT[C/G]AGAGACATTAAATGA	146691
rs754587372	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17901183	TTTATCTCTCTCCCC[A/G]GGGGAAAAGCTTCAG	146691
rs754601752	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17866540	CGCTGCTCTAGTACA[A/G]AAGCAAGGCCACTTC	146691
rs754604280	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17851389	GGGAAGGCCAAGTGA[C/T]AGCCTGCCCAGAGCG	146691
rs754681097	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17960613	AGAATACTAGTATTA[C/T]AGGCATGAGCCAGTG	146691
rs754685754	snp	A/G	1.64868e-05	0.00287109	synonymous-codon, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17879642	CTGCAGCAACTCCAG[A/G]TCAGATGAATCCTCC	146691
rs754690089	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17850357	TCATCTTCTAGCCCT[A/G]TCTCTGAGGATGGAG	146691
rs754753103	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17935886	TTCTGAGGAATGACT[C/G]ACACTGGTGGTGCCT	146691
rs754753295	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17942546	TATTATGGGCCGATA[C/T]GTATGGGCCGATATG	146691
rs754754378	snp	G/T			intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17860414	TGACCAGTGCAGAGG[G/T]ATGCATGCCCTCAGA	146691
rs754760541	snp	A/T	1.65803e-05	0.00287922	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17861460	TCCAGGCAGAAAAAC[A/T]GGGTTAAAGACCTAC	146691
rs754775951	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17896613	GCCGCTTTAGGCCAC[C/G]CTGCCAAACAGGACC	146691
rs754808358	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17955462	TCCAGCCTCCATCTC[C/T]CACGTAGCTGGGATT	146691
rs754813363	snp	A/G	1.67674e-05	0.00289541	intron-variant	TOM1L2	GRCh38.p7	17:17869496	ACACATGCACCTCTG[A/G]GTAGCCTGCTGGGTG	146691
rs754825396	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17909155	CACTGCATTCCAACC[C/T]GGGCGACAGAGCCAG	146691
rs754834329	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17875023	GCACTTTGAGAGGCC[A/G]AGGTTGGTGGATCAC	146691
rs754859688	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17923812	GGGAGACACTCCAGT[C/G]TGAGAGACAGAGCAA	146691
rs754887795	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17873781	AAAATAAGGGGGCTG[A/C]ATTCATGAGGAAGTT	146691
rs754896705	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17963541	TCTTCACCTGTAAGA[C/T]GAAGATAACAGTGCT	146691
rs754904790	in-del	-/TTAA			intron-variant	TOM1L2	GRCh38.p7	17:17949085	CAGGTCAGGGACACC[-/TTAA]TTGAGTGTTCTCAGG	146691
rs754911492	snp	A/G			intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17859051	GATTTGTAGAGGTGC[A/G]GCTACACGATTTTCT	146691
rs754922403	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17970632	AGAGACAAGATGTCA[A/C]AAAGGTGGGAAAACA	146691
rs754948319	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17854566	GTCTTGCTCTGTTGC[C/T]CAGGCTGGTGTGCAG	146691
rs754958272	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17887573	CCTCTGCCTCCGGGC[C/T]CAAGCAATCCTCCCA	146691
rs755028411	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17969246	ATTACTAGTAGAGAC[A/G]GGGTTTCACCATATT	146691
rs755080510	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17931572	TCTCTCCCCCTCCCC[C/T]GTACAAAATGAGCTC	146691
rs755082666	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17918672	CAACGTCCTCTCCAG[A/T]ACCTTCTTTGCTGCC	146691
rs755108630	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17927116	GAATAGGCATTTTCC[C/T]AGCTTTTCGGATTTT	146691
rs755133240	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17868399	AATGCAAGCATCTGT[C/T]CCACTCACCCTAACT	146691
rs755135730	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17930439	TGCAGAGACCCTCAC[A/G]GTAGACAGACACCTG	146691
rs755190785	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17963015	TCAGGTTTTTTTTTT[A/G]AAGAATAAATAGAAA	146691
rs755191571	snp	C/T	1.64798e-05	0.00287047	synonymous-codon, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17884766	AAAGGCATCAGCCCA[C/T]GCCTGGGATAATAGA	146691
rs755205741	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17877024	TTCACTCTGGGCACC[C/T]TTCCTTCCTTCTCCT	146691
rs755233238	snp	A/C	3.29468e-05	0.00405861	intron-variant	TOM1L2	GRCh38.p7	17:17869333	AAAAAAGAAATCCGG[A/C]TCCCACCTCTCGTAT	146691
rs755236976	snp	A/C/G/T	9.89736e-05	0.00703412	intron-variant	TOM1L2	GRCh38.p7	17:17848874	TCTGTGGGAGGAGCA[A/C/G/T]AGAAAATGAAATTAG	146691
rs755259062	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17893501	TAGAATTTCATTCCA[A/G]TGGGATGAGAATTTT	146691
rs755288399	snp	C/T	4.95062e-05	0.004975	intron-variant	TOM1L2	GRCh38.p7	17:17866974	AGGATGCCTGTGATA[C/T]GGCCCTGTGGGGTGC	146691
rs755317592	snp	A/G	1.66582e-05	0.00288597	intron-variant	TOM1L2	GRCh38.p7	17:17907430	AGAGGCTTCCCAGGA[A/G]AGGGGGGCACACGTA	146691
rs755357637	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17876823	GTCTAACCAAGATGT[C/G]CATTTGAAAGCAAGA	146691
rs755400946	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17925309	TGTAAGAAAAAAAAG[A/G]CACAAAATTGATTTT	146691
rs755425372	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17939540	GCTGAAATAATATGA[C/T]TTGGGGGACTTACTT	146691
rs755484609	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17938328	CCTGCTGTGCCTAAG[A/G]CCTTGCCCTCAGCAA	146691
rs755486569	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17952210	TACAATGACATGGCA[A/G]AACAAAAGCGAGCTG	146691
rs755488095	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17904308	AGGCATTGGCCCCTT[C/G]AGAATAAGGAAGCTC	146691
rs755506258	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17905296	TCACATCTTCCAGGA[A/G]CCTGGCTGGCAGCAA	146691
rs755529883	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17919858	TTAACCCTACCATCC[C/G]ACGCCCCAGCCGCCA	146691
rs755550378	snp	A/G	1.6543e-05	0.00287597	intron-variant	TOM1L2	GRCh38.p7	17:17879789	AAGGAAAGGTCAGTC[A/G]GCCTGCACTTGCAAT	146691
rs755558704	snp	C/G	1.65102e-05	0.00287312	intron-variant	TOM1L2	GRCh38.p7	17:17848803	AAAAGGGGGCTGTAA[C/G]GCCACTGGCCAGGCC	146691
rs755564555	snp	C/T			intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17861755	TAGGAGGCCTGGGTC[C/T]TAGCTCAGGCTGAGC	146691
rs755576657	snp	G/T	1.64776e-05	0.00287028	missense, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17884755	GGACTGCTTCGAAAG[G/T]CATCAGCCCATGCCT	146691
rs755601838	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17850033	CACCAGCCCACAGAC[A/G]GCCAGGCTGACCCTG	146691
rs755625943	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17893272	AAACATCCCTTAACA[A/C]CATCCCCAGCCCCTT	146691
rs755628234	in-del	-/G			intron-variant	TOM1L2	GRCh38.p7	17:17918268	TTTTTTTTGTTTTGT[-/G]GGTATCTTCAAGGTT	146691
rs755652930	snp	C/T	3.43578e-05	0.0041446	intron-variant	TOM1L2	GRCh38.p7	17:17893846	AAAGGGTCACCCCAG[C/T]GGGAGCTGGAGAAGA	146691
rs755654975	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17915696	AATTTTCTTTAAAAA[A/C]ATTTATGTAGAGATG	146691
rs755673239	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17946619	GTTAAGTCTGTTTTT[C/T]GCTAAACCACAAGTT	146691
rs755699776	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17958238	AAATGAGTAACTGAC[A/G]GGATGTGCCCCACCC	146691
rs755706938	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17924460	CTCAATAAAGCTGTT[C/G]AAAAATGGGAGAAAA	146691
rs755723692	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17864840	AGTCATATATGCTGG[A/C]CTGACTGAAGGCAGA	146691
rs755750801	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17888570	GCTGTCCACACAGAA[A/T]CTGGCCAGAGCCCAG	146691
rs755780359	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17956889	GAGGGAGGCGGCTCC[A/G]GCCTCGGCCAGCCCA	146691
rs755813631	snp	C/T	1.65034e-05	0.00287253	synonymous-codon, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17879735	CAGTTCACTCCGCAG[C/T]CTGGCAATCTGGTGG	146691
rs755821142	snp	C/T			intron-variant, downstream-variant-500B	TOM1L2, LOC100507131	GRCh38.p7	17:17858099	GTGCCCTTGGAAAAT[C/T]TCCAGGAGATCACAG	146691
rs755824410	snp	A/C			upstream-variant-2KB, intron-variant	TOM1L2, DRC3	GRCh38.p7	17:17973323	GAATTTAGCCATCAT[A/C]ACTGACCTCATAACT	146691
rs755832900	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17922504	GGAAGCAGGGGGCAG[G/T]TTATCACAACTGCTC	146691
rs755859155	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17879580	TCCAACAGTGTACGG[C/T]GGAAGAGCTGCCACC	146691
rs755869161	snp	C/T	1.64893e-05	0.0028713	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17879662	ATGAATCCTCCTGTC[C/T]AGGGACCATTTCTGT	146691
rs755874617	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17873564	ATTCCTCAGTAGACT[A/G]CAGGAAGTGTCTCAG	146691
rs755907701	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17872331	AACAATTAAAATAAT[C/T]ATAGTATTTCTAATA	146691
rs755964927	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17967998	ATGCACAGTTAACTA[C/T]GTCAGACTGTGGTCT	146691
rs755991564	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17934987	CACATAGCAATTAGA[A/G]TGGAACTCAGGGCAC	146691
rs756002024	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17941558	GATTCCAAGCCACGA[G/T]GAGATATCCACGGGC	146691
rs756006287	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17910948	GGATGTTGCTGAATG[C/T]AAAATGCTAAAACCA	146691
rs756007896	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17851211	GGAAGGTGGCTGTAC[A/G]CGTTCTTGAAATGGA	146691
rs756018909	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17886236	AAAAAGCCTCCTTAA[C/T]TATGACTGATGCATC	146691
rs756048395	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17948023	GTCAAGTGCTTTACA[C/T]GCATTATCCAATTTG	146691
rs756061321	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17939342	AGTCACCTCACTGTA[C/T]TTGTGATAGACCTTA	146691
rs756119930	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17933684	AGCCTGGTGGAGCCA[C/T]AATAGTTGTCTGATG	146691
rs756196956	snp	C/T	1.64871e-05	0.00287111	intron-variant	TOM1L2	GRCh38.p7	17:17884785	TGGGATAATAGAAGG[C/T]CTGTTAGGAAGCATT	146691
rs756213349	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17932304	TATTATTTTATTTTT[A/T]TTTTTTGTAGAGACA	146691
rs756217281	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17943828	CTGACTTCCACTTCC[C/T]ACCCCTTGCCAGGGC	146691
rs756274574	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17942398	AGTTCATTAATCCTG[A/G]CTTTAACCCTCAATC	146691
rs756282247	snp	A/T	1.6486e-05	0.00287102	missense, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17850951	GGCTGCGCAACGGGG[A/T]TCTATGGAGGCGGCA	146691
rs756326531	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17895294	ACGATGTCACCAGCA[A/G]CAGGGAACATTTCTG	146691
rs756369483	snp	A/C			intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17859058	AGAGGTGCGGCTACA[A/C]GATTTTCTCCCATTC	146691
rs756395091	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17955076	AAATGTGCCATCACA[A/G]GTGACATTTTCGGGT	146691
rs756399202	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17941481	AGCTAGACAAAAAGC[A/T]GAGAATCATCATTAC	146691
rs756401831	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17909061	TGGTGGGCACCTGTC[G/T]TTCCAGCTACTCAGG	146691
rs756417499	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17854510	ATTTTTATTTATTTA[G/T]TTAGTTATTTATTTA	146691
rs756419453	snp	C/G	3.29614e-05	0.00405951	missense, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17882746	CAGTCACACTCAGAG[C/G]TGGGGCCTGCGGTGC	146691
rs756461837	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17950711	TAATGCCAAGTGAAA[C/T]TACTTTTCAATTGAG	146691
rs756504060	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17890095	TCAGAGTCTCTGGGG[C/G]AGTCTTAAGTTTTCT	146691
rs756571338	snp	C/T			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17844312	ATCGGCAGCAGCTGC[C/T]CTGCGAGCATCTGTT	146691
rs756580129	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17949465	AGAGTCTTACAGGAT[A/G]AATACCACCCCACTC	146691
rs756607757	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17907634	TTCTTCTCCCAAGCA[A/G]ATGGGCTGAGCCAAC	146691
rs756673972	snp	C/T	4.95471e-05	0.00497705	intron-variant	TOM1L2	GRCh38.p7	17:17879757	ATCTGGTGGGGGCCA[C/T]GAGGAAGGAAAGCAG	146691
rs756682926	snp	C/G	6.59141e-05	0.00574045	missense, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17882782	AGGGAGCAGGAGGCG[C/G]CGAGGAATAGGAACC	146691
rs756683984	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17902537	TCAGTTTCCTTAACA[C/T]TGAAACAGGCTGTCA	146691
rs756742362	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17898448	CCCAAAGGCAATACC[A/G]GAAGGCTTTGCTGGA	146691
rs756743583	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17864847	TATGCTGGACTGACT[C/G]AAGGCAGAGACATCT	146691
rs756745031	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17962822	AAAATTTAGCTGGGC[A/G]TGGTGGCGCGTGCCT	146691
rs756748438	snp	A/G	1.65002e-05	0.00287225	intron-variant	TOM1L2	GRCh38.p7	17:17862854	GTCCCCAAGTCTGTG[A/G]CAACAAAACAAATGG	146691
rs756757857	in-del	-/AAA			intron-variant	TOM1L2	GRCh38.p7	17:17869309	CAATCTTTTCAAGGG[-/AAA]AAAAAAAAAAAAGAA	146691
rs756779415	in-del	-/TGACCGCTCTGGCTTCTTCCGGCCAGAAGGGTT	1.69395e-05	0.00291024	cds-indel, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847659	GAAGAGGGCATCCTC[lengthTooLong]TGAGGCTGGGGCAGG	146691
rs756788634	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17967637	TTGGAGATGCAGTCT[C/T]GCTCTGTCATTCAGG	146691
rs756819030	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17956262	TACAATCCCTGAGCT[A/G]GACACAAAGATTCTC	146691
rs756872535	snp	A/G			intron-variant, upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17971010	GAAGTCCCATATGGT[A/G]GCCATTTCAGTATTC	146691
rs756890215	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17876647	TGCGCCAGGCACTGC[C/T]AAGGTGCAAGTGATC	146691
rs756922125	snp	A/G	3.2993e-05	0.00406145	intron-variant	TOM1L2	GRCh38.p7	17:17862851	TCTGTCCCCAAGTCT[A/G]TGGCAACAAAACAAA	146691
rs756945299	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17892339	CCTTTGCCCTTGCTG[A/G]AGCCCCACGCCCAGC	146691
rs756977667	snp	C/T	1.64841e-05	0.00287085	missense, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17882725	CTGAATTGGCTGTGA[C/T]GGGGCCAGTCACACT	146691
rs756979700	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17893418	CCTACCTGCCTTTGT[A/G]AGCAGCAGAGGGATG	146691
rs757003275	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17918872	CTTGGAGGCAGGACA[C/T]CTTCATGTCAAGAAG	146691
rs757014791	snp	C/T	1.64757e-05	0.00287012	missense, upstream-variant-2KB, intron-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17862788	AACATGTCAAAGCCG[C/T]CACGGGGATTACATT	146691
rs757064319	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17849855	TTTCGAGACAGCCCC[C/T]TGGGAAAGATGTCCC	146691
rs757107426	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17899453	GGGCTCTGTCCAAAA[C/G]TTGGAGTGGAGCTGT	146691
rs757153371	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17933303	TTATGAAGAGGTGCT[C/G]TCCTCAGGAGCTCCT	146691
rs757197674	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17848751	GGGGCTCCAAGATGA[C/T]GGGGGCTGGCTCCTG	146691
rs757202307	in-del	-/A/C/CA	0.000225105	0.0106071	intron-variant	TOM1L2	GRCh38.p7	17:17869307	ACAATCTTTTCAAGG[-/A/C/CA]GAAAAAAAAAAAAAA	146691
rs757206728	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17931835	TTCCTATTTCACACA[A/G]TAAAGATCCTCTTCC	146691
rs757209796	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17958202	TCTTCAAAACAAACG[A/T]ACGAACAAACCATGC	146691
rs757254175	in-del	-/A			intron-variant	TOM1L2	GRCh38.p7	17:17941825	ACCTCATTTTGCCTT[-/A]AAGAGTTTCAGCCTC	146691
rs757264574	snp	C/T			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17845077	CAGGACAGGCCATCT[C/T]GCCAGGGCTAAGTGG	146691
rs757275238	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17874326	CCCAGGCTGGAGTAC[A/G]GTGGTACGATCTCAG	146691
rs757283586	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17894885	GCAATGAGCTAAGAT[C/T]GCGCCATTGCACTCC	146691
rs757287930	snp	A/G	1.6617e-05	0.00288239	intron-variant	TOM1L2	GRCh38.p7	17:17869478	CTGTTGAGCTCCTAG[A/G]GAACACATGCACCTC	146691
rs757323615	snp	C/T	1.6492e-05	0.00287154	intron-variant	TOM1L2	GRCh38.p7	17:17850962	GGGGATCTATGGAGG[C/T]GGCAAGCAGCGGGCC	146691
rs757330278	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17908018	CCTAGCACACAGTCA[A/G]TACTATACAGGTATT	146691
rs757342443	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17894050	CAATAATCAGGCAAT[C/T]AGTTGGTAATTGAGG	146691
rs757344032	in-del	-/C			intron-variant	TOM1L2	GRCh38.p7	17:17951187	CACTCCCTTGCGGGG[-/C]TGCAAGGAAAATGAC	146691
rs757401837	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17953981	GGCAAGCATTGTTCA[C/T]CTTTGAATTCAAAAT	146691
rs757459977	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17932898	GGCCCAGAAATCTGT[A/G]GGGATTTAAATTATT	146691
rs757486987	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17935878	TTAGCAAATTCTGAG[A/G]AATGACTCACACTGG	146691
rs757520450	snp	C/T	2.95164e-05	0.00384153	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17866401	CTATTAAGTTGTCTT[C/T]GGTTACTTCATTCAG	146691
rs757532875	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17952717	TATAATTTTTAAAAA[C/T]AAAAATGGGTCTCTG	146691
rs757532966	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17967732	TCCGCCTCAGCCTCC[C/T]GAGTAGCTGGGATTA	146691
rs757540054	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17962617	CCGCGACTGGCCCAA[G/T]GTGAATATATTTAAT	146691
rs757570434	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17872250	AACAAAATAAAAATG[C/T]CCAAACTTATGAAAG	146691
rs757570556	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17856831	CAGGCCACCTGAACA[C/G]ACAAGGCAGGAGAGA	146691
rs757574996	snp	C/T	1.64792e-05	0.00287042	synonymous-codon, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17882804	ATAGGAACCAGCACT[C/T]GTCCTCTGCTGTGAT	146691
rs757593770	snp	A/C	1.65236e-05	0.00287429	intron-variant	TOM1L2	GRCh38.p7	17:17884587	CAGCAGCTTGGCTCA[A/C]CCGTTCTGCAGTAGG	146691
rs757643958	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17902288	CAGCATTCCTCAGGC[C/T]GATGGTGACCTCAGC	146691
rs757682444	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17881130	AGGAGACCTCAATCA[A/G]TGGTCTACCAGGGAG	146691
rs757683577	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17866798	CCAGTTAGAAAAACT[A/G]GAGGTCTCTCCAGCC	146691
rs757696971	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17917194	AAAATTAGCTGGGCG[A/T]GGTGGCGCACACCTG	146691
rs757705065	in-del	-/G			intron-variant	TOM1L2	GRCh38.p7	17:17875848	GGGAGGGAGAAAAAA[-/G]TCTTTGTTGATGAGA	146691
rs757740528	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17928323	GATGGCTAAGCAACG[A/G]GGGTACATCAATAAG	146691
rs757741242	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17960895	TCGACTGAAAGATAA[A/G]GGCATGACACGGAAG	146691
rs757751528	snp	C/T	1.65116e-05	0.00287324	splice-acceptor-variant	TOM1L2	GRCh38.p7	17:17847785	GAATTTATCAAACTC[C/T]GCAATACAAACCAAG	146691
rs757780708	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17951771	GGAAGGAAGTTAGCC[A/G]AAGGCAACTTTCATC	146691
rs757784069	snp	A/G			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17846286	GCAGACTGACCCAGC[A/G]AGCTGGGCCCAAGAC	146691
rs757808183	snp	C/G	1.65285e-05	0.00287471	intron-variant	TOM1L2	GRCh38.p7	17:17862876	AACAAATGGGTGGCA[C/G]ATGAGAACAAAATGT	146691
rs757829832	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17915938	CTTTTCACTCTCTTG[A/G]TTGTATCTTTTAATG	146691
rs757857259	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17875149	GTAATCCCAGCTACT[C/T]GGGAGGCTGAAGCAG	146691
rs757868789	in-del	-/GACGG			intron-variant	TOM1L2	GRCh38.p7	17:17913180	GGGAGACCGTGGAAA[-/GACGG]CAGAGGGAGAGGGAG	146691
rs757903836	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17874145	TATTTTAATAGAGAC[A/G]GGGTTTTACCATGTT	146691
rs757904086	in-del	-/T			intron-variant	TOM1L2	GRCh38.p7	17:17955326	AGACCACACAATTCC[-/T]TTTTTTTTTTTTTTT	146691
rs757939533	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17923865	AAAAAAGGCCGGGCG[C/T]GGTGGCTGTCGCCTG	146691
rs757953244	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17868211	GCTCCTGTTCTCCAA[A/C]TGATGCACTGGGGGG	146691
rs757954961	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17888139	AAGTGATGCAGCGGT[A/G]TGAGCACACTCTGAG	146691
rs758083495	in-del	-/G	0.000200948	0.0100217	intron-variant	TOM1L2	GRCh38.p7	17:17869321	GGAAAAAAAAAAAAA[-/G]AAGAAATCCGGCTCC	146691
rs758116852	snp	C/T	4.37149e-05	0.00467499	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17866350	CTGTGTTCCCCACCA[C/T]TGGGCTCACCACGGC	146691
rs758170434	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17899170	CAAGTATTATTTATT[A/C]AAAACCCTAACTAAC	146691
rs758202376	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17944027	AGTGCATGCTGCTAC[A/G]TTATCAGAGCACCCC	146691
rs758205959	snp	A/T			intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17858853	CTCAAAGTGCTGGGA[A/T]TACAGGCGTGAGCCA	146691
rs758219410	snp	C/T	1.65652e-05	0.0028779	intron-variant, missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17893723	TCTTGGGAGATATAA[C/T]TTTGACCAGAACACT	146691
rs758226510	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17882629	ACCTGGCTTGGGAGG[C/T]CTTTGTAAGTGTCTC	146691
rs758256518	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17847850	AGGAAGCGCACCCTT[C/T]CACTCCCCAGCCCGT	146691
rs758261479	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17910279	AGGACTACAGCCAGG[C/G]TCACTTGACTCCCTT	146691
rs758279717	in-del	-/T			intron-variant	TOM1L2	GRCh38.p7	17:17934934	AAAGAGAAATGCGGG[-/T]TCATTACTCAGCCAC	146691
rs758285829	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17944854	TGCTCCCAGAGATGT[C/T]TGCCTGATGGCAATG	146691
rs758295939	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17855612	CTGGTGGTGTCAGTT[A/T]ACTTCTGTGTTGGCT	146691
rs758310693	snp	C/T	0.000133318	0.0081634	intron-variant	TOM1L2	GRCh38.p7	17:17869486	CTCCTAGGGAACACA[C/T]GCACCTCTGGGTAGC	146691
rs758319915	snp	A/C	3.32646e-05	0.00407814	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17861443	CTTTCCCTCCAGAAG[A/C]CTCCAGGCAGAAAAA	146691
rs758346271	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17884925	TCCTCTCCTTCCGCA[A/T]CTGCTGCCACGACAC	146691
rs758346630	snp	C/T			intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17860718	GCAAACAGACGTGCA[C/T]TCATACACATTTCTT	146691
rs758361755	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17892650	AACATTCTTCATTAC[A/T]CCCCCTTCCCCACAT	146691
rs758404280	snp	C/G/T	5.04641e-05	0.00502294	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17861602	TTCCTCCAGTGGTCA[C/G/T]GGAGGGATGGGGTAG	146691
rs758412091	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17909388	TAAGCCAAATGGATA[C/T]ACATATAATGGATTA	146691
rs758426615	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17906512	ACAGTCTTGTCCTCA[C/T]CTGACCAGGTTATAT	146691
rs758463932	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17956216	CAGAGACCTGATTGG[C/T]CTATTTTGACAGGGT	146691
rs758474305	in-del	-/A			intron-variant	TOM1L2	GRCh38.p7	17:17925238	ATGCAAGAACAACCT[-/A]ATACAGCCATTATAA	146691
rs758481814	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17905612	GACACCGTCCTGGTT[C/G]ATCACAGCCTCGAAC	146691
rs758514219	in-del	-/TCT			intron-variant	TOM1L2	GRCh38.p7	17:17849026	ATAGTAAAATACTGC[-/TCT]TCTTATTGGAGAAAC	146691
rs758591917	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17871166	ACGAGGTCAGGAGAT[C/T]GAGACCATCCTGGCT	146691
rs758609449	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17919906	TAATAGGAAGAAAAT[A/G]AAGCCTGGTGGGGTG	146691
rs758609639	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17874432	CCCGCCACCACACCC[A/G]GCTAATTTTTGTATT	146691
rs758623530	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17880014	GTAGTGAAGGGCTCC[A/G]TGTCAGGAGTGCACC	146691
rs758651903	snp	A/G	4.95569e-05	0.00497755	intron-variant	TOM1L2	GRCh38.p7	17:17847812	CAAGGCAAGGGTCAG[A/G]GTTGGTGAGGGCAGG	146691
rs758656068	snp	A/T			upstream-variant-2KB, intron-variant	TOM1L2, DRC3	GRCh38.p7	17:17974309	CTCAGTACTTTTGCA[A/T]TTCTCAGTACTGTTG	146691
rs758669501	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17884146	CTGATGGAATCAAGG[A/T]TTGAATCCAGAATCA	146691
rs758684271	snp	C/G/T			intron-variant	TOM1L2	GRCh38.p7	17:17931798	GACACTGTTAGCCCC[C/G/T]TGAGGGTCTCAACAC	146691
rs758734665	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17938400	GATTTCACTGCAGTG[A/G]CCTGAAGCTGCCTTC	146691
rs758794418	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17865169	GGTGAGTTTCTTTTA[A/C]GTTCCAGACAATGGA	146691
rs758800169	snp	C/G	1.64787e-05	0.00287038	intron-variant	TOM1L2	GRCh38.p7	17:17866944	CAGGGGAAGGGAAAG[C/G]AGAAGTAAGGAGAGA	146691
rs758847316	snp	C/G	1.64751e-05	0.00287007	intron-variant	TOM1L2	GRCh38.p7	17:17866866	GACAGGATTCTGAAG[C/G]AATACTTACTCCATT	146691
rs758849357	snp	A/G	3.29457e-05	0.00405854	synonymous-codon, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17884679	GTCCAAGTCTGCCAT[A/G]GGAAATTCAACCCCT	146691
rs758855995	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17878270	CAGGTGTGTCAGGAG[C/T]GAGGTCTGGGAACTA	146691
rs758863474	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17928199	TAAAACCATTCATAA[C/T]TTTGACCCGGCAATA	146691
rs758869712	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17897197	AGAGCTCATTCCCTC[A/G]TGATATGAGTTATTG	146691
rs758873319	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17893561	AATGTAGAAGTCTCC[A/T]TTTTTTTTTTCCTCC	146691
rs758903284	snp	G/T			upstream-variant-2KB, intron-variant	TOM1L2, DRC3	GRCh38.p7	17:17973591	AGTAAGTGATTGATT[G/T]TATTCTTTTTTAAGA	146691
rs758919288	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17926730	GGGCCTGGTAGCACA[C/T]GCCTGTAATCCCAGC	146691
rs758949960	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17869209	GGAACAAATTAGCAT[C/T]TCTGATGAGTATTTT	146691
rs758951721	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17857573	AGGGAGGTATTTTTG[A/G]GACTGGGAATCTGTG	146691
rs759002706	snp	C/T	9.88354e-05	0.00702908	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17898627	ACCTCTCTGTAGTTC[C/T]GGTTCCCGTTGAGCC	146691
rs759067702	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17963569	GCTTCCAGAGAAAAA[A/C]ATTTTTAAATGAGAT	146691
rs759069442	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17949031	AGAGTGACTGTCCCA[A/T]AGACCAGAGAATGGG	146691
rs759173361	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17875704	TTATCTTTTCTTCAA[A/G]GGACATTCTCATCTC	146691
rs759186241	snp	C/T	2.25828e-05	0.00336019	intron-variant	TOM1L2	GRCh38.p7	17:17869288	GAAATCCCTCTGTTA[C/T]GGCAACAATCTTTTC	146691
rs759204570	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17897203	CATTCCCTCGTGATA[C/T]GAGTTATTGAAAGCC	146691
rs759206629	snp	C/T	1.64749e-05	0.00287005	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17866920	CAGACCTGTATCGTT[C/T]GAACCTAACAGGGGA	146691
rs759231778	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17873772	TCCCTGGGTAAAATA[A/G]GGGGGCTGCATTCAT	146691
rs759252685	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17880888	TGTGACCCAGCTTAA[A/G]TGACAACTTCTCTCC	146691
rs759258458	snp	A/G			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847336	CGGGTGGTCTGCTCA[A/G]GAAGCACTGCCTGGG	146691
rs759271794	snp	A/C	1.64863e-05	0.00287104	intron-variant	TOM1L2	GRCh38.p7	17:17850844	CTGTCCTCAGAAGAG[A/C]CTCTGCCGCTCCACA	146691
rs759305150	in-del	-/CT			intron-variant	TOM1L2	GRCh38.p7	17:17856988	TGAGAGGGAGTCTCA[-/CT]CTATCACCAGGCTGG	146691
rs759309557	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17863669	TCCTCCCACCTTGGC[C/T]TCCCAAGTAGCTAGG	146691
rs759327052	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17939021	ACCCAAGTGTTTCAC[C/T]AATAAGTTATAATGC	146691
rs759341306	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17895329	CCTCAATTATTCTCA[C/T]TTGCCCAAACTAATC	146691
rs759356488	in-del	-/A			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847449	GTTGTCCCACCACTC[-/A]AGAGAAAAGAAGTGG	146691
rs759362498	snp	C/T	1.65501e-05	0.00287659	intron-variant	TOM1L2	GRCh38.p7	17:17898702	ACAGACATATAAAGA[C/T]ACTTACAATCCCACT	146691
rs759371425	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17889547	GGCTTTGGCCAGCAG[C/T]TGGTAATCAGAGCCA	146691
rs759378806	snp	A/G			intron-variant, upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17971714	GTGGCATCTCCCAAA[A/G]CGCATTGGGGAAGCA	146691
rs759427861	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17966633	AAAAGTAACATAAAT[G/T]GCAGCACAGAATGAG	146691
rs759443246	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17953923	AGGATGCCTTCCCTT[C/G]TACCCTGTACAGTTA	146691
rs759473696	snp	A/G	1.64798e-05	0.00287047	synonymous-codon, intron-variant	TOM1L2	GRCh38.p7	17:17862832	GAGGGTGCCACTGAC[A/G]CTCTCTGTCCCCAAG	146691
rs759491810	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17904780	GACAGCTTGTATCCC[G/T]TGACACACTGGCCCT	146691
rs759501836	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17937582	GATTGAGGACCCCAA[C/G]TCATGCAGGCTTTGC	146691
rs759540134	snp	C/T	6.61299e-05	0.00574983	intron-variant	TOM1L2	GRCh38.p7	17:17882689	GCTTGCCTATGGCCC[C/T]GAAGTATGCAAGTAC	146691
rs759581127	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17853894	AAATAAGGCGATTGC[C/T]AGATTGTATTTGGCT	146691
rs759595245	snp	C/G	1.64871e-05	0.00287111	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17907481	TGATGTCACAGATCT[C/G]CATATTCAACGTCCA	146691
rs759595372	snp	C/G	1.65031e-05	0.00287251	synonymous-codon, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17879729	GACGTCCAGTTCACT[C/G]CGCAGCCTGGCAATC	146691
rs759618925	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17944786	ACAGGAGGTCCGCAC[C/T]TGTGCTCTCCATATT	146691
rs759620108	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17900049	AAACCCCGTCTTTAC[C/T]GAAATATACAAAAAT	146691
rs759620232	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17886202	AACAGACCCATTTGA[A/C]GTTAAAAGGTCAGTT	146691
rs759629277	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17871012	AGGTATTTCCCTGGT[A/T]CCCATGACACATGGG	146691
rs759670779	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17863646	CCTTGACCTCCCGGG[A/C]TAAGTGATCCTCCCA	146691
rs759692024	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17946193	GTAATTCAATTTTGT[A/G]TAAGAGCTTTATTGA	146691
rs759709360	in-del	-/CT	4.64371e-05	0.00481834	intron-variant	TOM1L2	GRCh38.p7	17:17869250	TCTCTCTCCCTCTCC[-/CT]CTCTTTCCTTTGTTT	146691
rs759716524	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17914453	AGGCCCAGGTCTGCT[A/C]CTTGCTGGCTTTATG	146691
rs759741029	snp	C/G/T			intron-variant	TOM1L2	GRCh38.p7	17:17956647	GCCCCGCAGGGAGAC[C/G/T]GCTGAGACCCGGCGA	146691
rs759742577	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17957562	AAAATGTATGCATTT[A/T]ACTACAAGTAAACTA	146691
rs759751295	snp	C/T	1.66062e-05	0.00288146	intron-variant, missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17893776	ACAAGGATGTGGAAG[C/T]GGTGGCCACAGTTCT	146691
rs759758595	snp	G/T			intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17862467	AAAAGAGAAAAGCTG[G/T]CTCTTACAACTGACA	146691
rs759762655	in-del	-/G	1.66579e-05	0.00288595	intron-variant	TOM1L2	GRCh38.p7	17:17907431	AGGCTTCCCAGGAGA[-/G]GGGGGGCACACGTAC	146691
rs759769484	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17906965	GCAGGAATGCAGGAG[C/G]GGCAACGTGTTCTAA	146691
rs759775536	snp	C/T	1.6865e-05	0.00290383	synonymous-codon, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847662	GAGGGCATCCTCTGA[C/T]CGCTCTGGCTTCTTC	146691
rs759783053	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17877545	TGGGAGACCCTGCCT[A/G]CTGGCTTTTGACTGC	146691
rs759787784	snp	C/G	1.65806e-05	0.00287924	intron-variant, missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17893682	CAGAGCAAGCACTTT[C/G]TCCTGTACAATGGTG	146691
rs759803066	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17910920	GCTGTTTTCTTCTCC[A/G]TTCTCACCAAAAGGA	146691
rs759890583	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17967128	CAATCTGAGGGACAA[C/T]TAACTATTCTTGGTA	146691
rs759902409	snp	G/T			upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17972644	GGGAAGCTGCGCATT[G/T]TGATTCCTCTGTATA	146691
rs759908385	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17907573	TACATTTCTCCTGGA[A/G]TAAGTGGGCCTTGGC	146691
rs759911481	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17922393	ACAGGAGGCAACATG[C/G]GGCTTTTCAACAGGA	146691
rs759965313	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17968448	AAGGAGGGTGGATCA[C/T]GAGGTCAGGAGTTCA	146691
rs759982924	snp	A/G	1.65422e-05	0.0028759	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17869451	ATGCGCTGCTGCATG[A/G]CCCGACAGGTCCTGT	146691
rs759998682	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17953317	GTAAATGTTATGTTA[C/T]GTGTATTTTACCACC	146691
rs760011535	in-del	-/C			intron-variant	TOM1L2	GRCh38.p7	17:17915656	AAGTAGCTGGGACTT[-/C]AGGGATGCACCACCA	146691
rs760030159	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17934247	CCCAGGAGTTCAAGA[C/T]CAGCCTGGGCAACAT	146691
rs760034205	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17921012	CTATTAACTGAACTC[C/T]AGATGTTATTTGGAT	146691
rs760050360	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17927812	TGGGACTACAGGCAT[A/G]TGCCACCACACCTGG	146691
rs760075995	snp	A/T			intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17858240	CATTTTTTTTTTCTC[A/T]TTTCTAGTGGCATGT	146691
rs760077767	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17931585	CCCGTACAAAATGAG[A/C]TCCTTGAAAGGCAAT	146691
rs760083379	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17932692	ACTTTAAAATATTGG[G/T]GTAAGGTGTTTCAAC	146691
rs760086012	in-del	-/TAAC			intron-variant	TOM1L2	GRCh38.p7	17:17928531	GCGACACCCTCCCTT[-/TAAC]TAACACTCAGCTCGT	146691
rs760086238	snp	A/G	0.000186968	0.00966691	intron-variant, downstream-variant-500B	TOM1L2, LOC100507131	GRCh38.p7	17:17857752	CAGCAGGCTTGGCTC[A/G]GCTGGTGACTCCTCA	146691
rs760105625	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17929024	TAACAAGTCTCATTG[C/T]TATGGTTCCTAATAC	146691
rs760132671	in-del	-/CAA			intron-variant	TOM1L2	GRCh38.p7	17:17931004	AATATGGAATGTCTT[-/CAA]CAACAGTTTCATATA	146691
rs760141683	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17885149	CTGGAGCCTTGTCAG[C/T]TCAGCAGGGTGCCTG	146691
rs760159436	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17965738	CCTTCCTCACAGCAT[C/T]GTTGTGAGGATCGAA	146691
rs760165652	snp	A/T	1.70915e-05	0.00292326	intron-variant	TOM1L2	GRCh38.p7	17:17869315	TTTCAAGGGAAAAAA[A/T]AAAAAAAAGAAATCC	146691
rs760172598	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17895872	GATCAGAGGTACCAT[A/G]TAACTTAACCTAGGA	146691
rs760206829	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17880734	CTCACCTACAGAAAG[A/G]TGGCACTAACCTCAC	146691
rs760343103	snp	A/C	1.64857e-05	0.00287099	intron-variant	TOM1L2	GRCh38.p7	17:17850853	GAAGAGCCTCTGCCG[A/C]TCCACACCCCACAGA	146691
rs760353750	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17894647	AATACGTTTAAAGCA[C/T]AGGCCGGGCATAGTG	146691
rs760408888	snp	C/G			intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17858406	CAGCCTCCTGAGTAG[C/G]TAGAATGACTTTTTC	146691
rs760440231	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17954580	GGCCTCCCAAAGTGC[C/T]GGGATTACAAGTGTG	146691
rs760476621	snp	A/G	0.000108584	0.00736749	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	TOM1L2, DRC3	GRCh38.p7	17:17972335	TGGACAACACGCAGC[A/G]GCCCGGGCCCCCTGT	146691
rs760507746	snp	C/G	1.64885e-05	0.00287123	missense, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17882710	ATGCAAGTACCTGTT[C/G]TGAATTGGCTGTGAT	146691
rs760519347	in-del	-/AGAAGTCAAT			intron-variant, downstream-variant-500B	TOM1L2, LOC100507131	GRCh38.p7	17:17857891	CAAGACCCATGAGAA[-/AGAAGTCAAT]AGCACATATTGTGGA	146691
rs760525091	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17903066	GCACTCTGTAAGACT[C/T]CAGTCTGGTGTCACT	146691
rs760571858	in-del	-/C			intron-variant	TOM1L2	GRCh38.p7	17:17898711	AAAGATACTTACAAT[-/C]CCCACTTGAGGACAC	146691
rs760574577	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17852313	GGTTGACACCTGCTG[C/T]TGATGGTGGGGGAGG	146691
rs760633519	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17917839	TTACACCTGTCATTT[C/G]ATCTACTCAGGAGGC	146691
rs760649428	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17962384	GGAGTGCAGTGACAC[A/G]ATCTTAGCTCACTGC	146691
rs760685544	snp	C/G	2.03942e-05	0.00319323	synonymous-codon, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17866330	GGAGAGGGAAGATGG[C/G]GGCGCTGTGTTCCCC	146691
rs760692632	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17867597	ATGAGGTGTGTGTTG[G/T]GGTGGGGCAGAATAG	146691
rs760704865	snp	A/G	1.65685e-05	0.00287819	intron-variant, missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17893699	CCTGTACAATGGTGG[A/G]AGGGTTGTTCTTGGG	146691
rs760746771	snp	C/T	1.64841e-05	0.00287085	missense, intron-variant	TOM1L2	GRCh38.p7	17:17862837	TGCCACTGACGCTCT[C/T]TGTCCCCAAGTCTGT	146691
rs760766914	snp	A/G			intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17860723	CAGACGTGCATTCAT[A/G]CACATTTCTTTGTTA	146691
rs760786075	snp	C/T			intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17862319	CCTCTGCTCTGACCA[C/T]TTATTTTAGTCAGGA	146691
rs760795691	in-del	-/A			upstream-variant-2KB, intron-variant	TOM1L2, DRC3	GRCh38.p7	17:17973179	GTCAAGCTTTTGAAT[-/A]AAAAAAAAAAAAAAT	146691
rs760807390	in-del	-/G			intron-variant	TOM1L2	GRCh38.p7	17:17886775	TTCTCTCCAGTTGGA[-/G]GGATACTTCTTCGGG	146691
rs760831811	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17874895	CTTCCACATCAGGGA[C/T]TTCCAGGGGTCTCTG	146691
rs760843312	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17956566	GCGCTCCTTGGGGAG[G/T]TTCGGGCCGCATAGG	146691
rs760854771	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17937470	ATGGTGAGGGCCAAA[A/G]ATCTGTAGCAAATGA	146691
rs760889847	snp	C/T			intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17858251	TCTCTTTTCTAGTGG[C/T]ATGTGTATTCTTTTT	146691
rs760898362	snp	C/T			intron-variant, upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17971494	TCCTATCCCAGTCCC[C/T]CCTACAGCACAGCTG	146691
rs760905456	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17876031	CTTATGCTGATGAAC[G/T]GCCACAGAAGAACAT	146691
rs760911204	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17890685	GGAACAGAGAAGACT[C/T]GTCTATGCTGTGAGA	146691
rs760939410	snp	C/T	1.656e-05	0.00287745	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17869463	ATGGCCCGACAGGTC[C/T]TGTTGAGCTCCTAGG	146691
rs760944836	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17886851	GGAGTGGGAGGGAAA[C/T]GCACACCCAAGTTGG	146691
rs761009861	in-del	-/G			intron-variant	TOM1L2	GRCh38.p7	17:17872923	CACAAGGCACAGGAC[-/G]GTGCAAGTCAGGGGA	146691
rs761014624	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17883663	GGCGTGAACCCAGAA[A/G]GCGGAGCGTGCAGTG	146691
rs761027324	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17923607	AGGCAGGAGGATCAC[C/T]TGAGGCTAGGAGGTC	146691
rs761031922	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17932394	CTTAGCCTTCCAAAG[G/T]GCTGGGATTACAGGT	146691
rs761036412	snp	C/T	0.000551521	0.0165969	intron-variant, synonymous-codon, downstream-variant-500B	TOM1L2, LOC100507131	GRCh38.p7	17:17857841	ACCTCTCTTCTGGGC[C/T]GAGGACAGAAAAGTC	146691
rs761037887	in-del	-/CT			intron-variant	TOM1L2	GRCh38.p7	17:17910022	CAACAGAGTAAGACC[-/CT]GTCTCTTAAAAAACT	146691
rs761069513	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17898948	CATAAAGTTCTTTGC[A/C]TAACAGTGTACAAAG	146691
rs761112529	snp	A/C	3.30677e-05	0.00406605	missense, upstream-variant-2KB, intron-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17861530	AAGTCCTCCGACAGC[A/C]TGAGGATCCTCATAG	146691
rs761125918	in-del	-/TA			intron-variant	TOM1L2	GRCh38.p7	17:17943361	AGGCAAAGCAGTCTC[-/TA]TATAGGGGTCAGATA	146691
rs761156360	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17946088	TCATGTTGGAGACCA[C/G]GCTGGTCTCCAACCC	146691
rs761166684	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17931321	CACTGCCAAGCAAGG[C/T]AGAGCACCAACAAGG	146691
rs761215696	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17935874	CAATTTAGCAAATTC[A/T]GAGGAATGACTCACA	146691
rs761221909	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17944761	GCTATGGAAGCCTTC[C/T]GGCGGGGAAACAGGA	146691
rs761224631	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17882390	TTAAATGTCATTGCT[A/G]AGCATGCGGTCTCAC	146691
rs761264925	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17927477	TAAAGAACTCAACCT[A/C]AATGTGATACATCAA	146691
rs761266752	snp	C/T	4.95454e-05	0.00497697	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17907519	CTTTGCAGGGAGCCA[C/T]CTGTTGCCTTTTCTG	146691
rs761344002	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17877958	CTGCTCTGGCTGTCT[A/G]GAAGCATCTTGGCTT	146691
rs761384051	in-del	-/CT			intron-variant	TOM1L2	GRCh38.p7	17:17946310	ATCACCACTATGTAA[-/CT]CTAGAATATATTCAT	146691
rs761402820	snp	A/G	1.65086e-05	0.00287298	intron-variant	TOM1L2	GRCh38.p7	17:17850994	GGCAGCCCCCACACA[A/G]CCAGCGAGGGGAGAC	146691
rs761427311	in-del	-/TTA			intron-variant	TOM1L2	GRCh38.p7	17:17932288	TTTATTTCATTATTC[-/TTA]TTATTTTATTTTTAT	146691
rs761451871	snp	A/G	2.07531e-05	0.0032212	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17866337	GAAGATGGGGGCGCT[A/G]TGTTCCCCACCATTG	146691
rs761458506	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17856203	TGGGCTGGATCTTCC[A/C]AATGAATGGACATGG	146691
rs761469248	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17893360	CGTAGCTCTAACATG[A/G]TTCTTCCTACTCCAA	146691
rs761488768	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17867433	GCCAGTAGCTGCTAC[A/G]GAGAGGCCTGGGCCA	146691
rs761489869	snp	C/G	0.000109284	0.0073912	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	TOM1L2, DRC3	GRCh38.p7	17:17972349	CGGCCCGGGCCCCCT[C/G]TCTGCCACCTAGGCC	146691
rs761544512	in-del	-/A			intron-variant	TOM1L2	GRCh38.p7	17:17958117	AAGAAAAGAAAAACT[-/A]AAAGCCACTTTGATT	146691
rs761548279	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17953064	GTGGGCAGATCACTT[A/G]AGGCCAGGAGTTTGA	146691
rs761553098	snp	A/G			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17844884	ATTAGTGCTTATAAG[A/G]AATCCCAGCAATAAT	146691
rs761584609	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17851042	GAAATCATCAACAGC[A/C]ACCCCAAATAAAACC	146691
rs761599783	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17966831	TGGTACTTAATAATT[A/G]TAAGTTCCTTCCAGT	146691
rs761605630	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17956102	AACAAAGCCTCCCCC[A/G]CACGAAAAAGGACCC	146691
rs761638997	in-del	-/ACAT			intron-variant	TOM1L2	GRCh38.p7	17:17894935	AACTCTGTCTCAAAA[-/ACAT]ACATACATACATACA	146691
rs761643258	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17851136	CGTGTGAGATGGCAG[A/G]TGAGGAAAGCAATGA	146691
rs761653220	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17916580	AAATCAATTGACCAT[A/G]TACGGGAGAGTTTAT	146691
rs761708172	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17915418	GTTTTGTATTTCTCT[A/G]ATGACTACTGATGTT	146691
rs761723092	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17900427	CTCTGGAGGCTGAGG[A/C]AAGAGAATTGCTTGA	146691
rs761731410	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17866047	GCGCACGGCCGTGAC[C/T]TTTCTTTAATTCATT	146691
rs761736347	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17947834	GTACAACAAGTTGTA[C/T]TCATTTTTAATTTCT	146691
rs761758453	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17924170	AGGTAAAAATGACTA[C/T]ATATTGTATGATTCC	146691
rs761760720	snp	C/T	3.29571e-05	0.00405924	intron-variant	TOM1L2	GRCh38.p7	17:17898559	GGAGCAAGGAGTTCC[C/T]CAGATGACTTCTCTC	146691
rs761812249	snp	G/T	8.26262e-05	0.006427	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847731	GGGGGGCGAGGGGAG[G/T]TCGGGAACCATTTCA	146691
rs761832063	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17938026	TTTTGCCATACGGTG[A/G]CTCTGCTTTGGAGGG	146691
rs761861107	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17949574	GACAGTGGCTCTCTG[A/G]TCAGAGGACATATCT	146691
rs761867100	snp	C/T	1.66344e-05	0.0028839	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847682	CTGGCTTCTTCCGGC[C/T]AGAAGGGTTTGAGGC	146691
rs761867412	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17879215	AAATGTGATGTTGAG[A/G]GACCAAAATACAGAA	146691
rs761878501	snp	A/G			upstream-variant-2KB, intron-variant	TOM1L2, DRC3	GRCh38.p7	17:17973998	GTTGGGTGGTAAACT[A/G]TAAGATCCCCATAGA	146691
rs761903481	snp	C/T	6.60939e-05	0.00574827	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847733	GGGGCGAGGGGAGGT[C/T]GGGAACCATTTCAGC	146691
rs761911675	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17895014	TAATGCACATAGCAA[A/G]GTATCCTGCATAGGG	146691
rs761921998	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17887157	TTCTCTTTGCCTAGG[C/T]AAGCTGGAGTTGGCA	146691
rs761932492	snp	C/T			intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17858837	CCACCCACCTCAGCC[C/T]CTCAAAGTGCTGGGA	146691
rs761957749	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17968805	ACAGATGTGCCTGTG[A/C]CCCACTCCCTGCCTC	146691
rs761971210	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17852142	TAGCTGGCTTCACCC[A/G]ATGCCATGATCTAGG	146691
rs761984725	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17968342	GGGAAAATTAGGTCC[A/G]AAGAGACTAAAAGTT	146691
rs762021018	snp	C/T	1.64942e-05	0.00287173	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17879703	GACATGACTTTTGTG[C/T]TTCCTCGAACGACGT	146691
rs762021743	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17888943	GAAGCTGAAAGCTGC[C/T]GGAAGGGAAGTCTTT	146691
rs762074469	snp	A/G	1.65102e-05	0.00287312	intron-variant	TOM1L2	GRCh38.p7	17:17879605	GCCACCACAGGCCAA[A/G]TGCTTCTGAAAGATG	146691
rs762091820	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17930192	CTGGAATGCTGACAC[C/T]ACTCATTATGCAGTC	146691
rs762120575	snp	C/T			intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17860827	AAAGCATGGTTATGT[C/T]TGGGGAGGCCCAAAC	146691
rs762171971	in-del	-/AGG			intron-variant	TOM1L2	GRCh38.p7	17:17901280	GTGGAGTTGGAAACC[-/AGG]AGAAGAGACAGAAGC	146691
rs762178172	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17934669	TTTTTAAAAATGTGT[C/T]GACCTATACAGCCAT	146691
rs762181239	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17879298	AAATACATCAAAGCA[C/T]CTACAGTGGTTATTT	146691
rs762214201	snp	A/G	1.64768e-05	0.00287021	intron-variant	TOM1L2	GRCh38.p7	17:17866937	AACCTAACAGGGGAA[A/G]GGAAAGCAGAAGTAA	146691
rs762216940	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17918177	ATATTAACAGAAACA[A/C]AACTGATTTTTGAAT	146691
rs762225035	in-del	-/GT			intron-variant	TOM1L2	GRCh38.p7	17:17891785	AAAGTGCATGCACAC[-/GT]GTGTGTGTGTGTGTG	146691
rs762230059	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17897280	ATTCTGAGAAAAAAT[A/G]AAATAAAAGCTTCAA	146691
rs762265362	in-del	-/CTGGAGGGAG			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17845986	ACAGAGGTTTCCTCT[-/CTGGAGGGAG]CTGGAGGGCTGCTAG	146691
rs762307732	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17914945	CAGACAGAAGACTGT[G/T]GCACAAATGTTTTGA	146691
rs762314372	in-del	-/A			intron-variant	TOM1L2	GRCh38.p7	17:17853073	GGGTACACTGCTACT[-/A]CTGTGCTTGCTGGCA	146691
rs762322988	snp	C/T			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847375	ACTCTGCCCGCTCTT[C/T]CTGGGAGGAAACATG	146691
rs762348623	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17955973	CCTCCCAATGGGTTC[C/G]TGGTCTGCGCCAGCC	146691
rs762370551	snp	A/G	1.64741e-05	0.00286998	synonymous-codon, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17884742	GCCGGTGAGATCAGG[A/G]CTGCTTCGAAAGGCA	146691
rs762404352	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17951745	GCATTTCCATGGGGA[C/T]GTGGTGCTTAGGAAG	146691
rs762405956	snp	A/G	1.64787e-05	0.00287038	missense, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17882778	GAGTAGGGAGCAGGA[A/G]GCGGCGAGGAATAGG	146691
rs762433168	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17870663	TAACTGATTTATTCA[C/G]AGGAGACACGGCAAT	146691
rs762484758	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17905904	TCGGTAACTTCCTCT[C/T]CAGGTACTCTCTTCT	146691
rs762566400	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17906805	ACTCCTGAAAATGGT[A/T]TAAGAGGGCATGGCT	146691
rs762585210	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17854276	AAACTGTGGGAGGCC[A/G]AGGACGCGCTCCTTG	146691
rs762612347	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17914711	TAGCCCCTGCCCAGT[C/G]CTCTGGCTGTGTATT	146691
rs762619592	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17883351	AACACTGCTCTCTGT[C/T]ATTATTAGAAGAATG	146691
rs762640105	snp	C/T	1.64931e-05	0.00287163	missense, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17882851	TCGCAGCTGGATCCA[C/T]TTCAGGGACACTCTG	146691
rs762675374	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17869561	TTTGTACTGATTCTT[A/T]AAAGTCACAAAAGGA	146691
rs762732382	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17963703	AGAGTGAATAACTAT[A/G]AAGAATATACTCTAC	146691
rs762750960	snp	C/T	1.64741e-05	0.00286998	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17866911	CGGATCGGCCAGACC[C/T]GTATCGTTCGAACCT	146691
rs762782172	snp	A/G	1.64914e-05	0.00287149	intron-variant	TOM1L2	GRCh38.p7	17:17898679	CATCCTTTGGCCTGG[A/G]AAAAAGAACAGACAT	146691
rs762814951	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17923673	CCAGCCTGGGCAAGA[C/G]GGTGAGACCCCATCT	146691
rs762818553	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17911096	CTGCCTTAGGTTTCA[C/G]AGAACATAGGAGGGT	146691
rs762860877	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17957981	TGTAGTCCTAGCTAT[C/T]CAGCAGGCTGAGGCA	146691
rs762869521	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17926224	CAAGCTGGCCTAAAC[A/T]TAAGTAAGCTTCATT	146691
rs762872409	snp	G/T	1.64966e-05	0.00287194	synonymous-codon, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17879714	TGTGTTTCCTCGAAC[G/T]ACGTCCAGTTCACTC	146691
rs762877497	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17940411	AAAGTATGATAACTT[A/G]TCCAAAAAGTCATGC	146691
rs762920433	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17947364	TTGTAGGCTAAATTG[A/T]GCCATCCTCAAGTTC	146691
rs762920451	in-del	-/AC			intron-variant	TOM1L2	GRCh38.p7	17:17885029	TTCCTTGGAGAAGAG[-/AC]AGAGAAATAACACCT	146691
rs762931310	snp	A/G	1.64985e-05	0.0028721	intron-variant	TOM1L2	GRCh38.p7	17:17879618	AAGTGCTTCTGAAAG[A/G]TGACTCACCTGCAGC	146691
rs762967900	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17893146	CTCTCTTTGATGCGT[C/T]TGGGCCTTTGCACAT	146691
rs762976114	snp	C/T	1.65263e-05	0.00287452	intron-variant	TOM1L2	GRCh38.p7	17:17848784	CAGCCTGCACAGAGG[C/T]AACAAAAGGGGGCTG	146691
rs762992435	snp	C/G	1.64776e-05	0.00287028	intron-variant	TOM1L2	GRCh38.p7	17:17898572	CCCCAGATGACTTCT[C/G]TCCTCAAGGAGAATA	146691
rs762997818	in-del	-/C	0.000165573	0.00909719	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17862720	AGCCACTAAAAGGGG[-/C]CCCCACATACGTCTT	146691
rs763013628	snp	A/T			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17843786	ATTAAGTGCAAACTT[A/T]AGGAAATAAATATCC	146691
rs763035617	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17922490	AGAGACTGCAGGCAG[C/G]AAGCAGGGGGCAGGT	146691
rs763069178	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17932846	TGAGTCCCATCCCCA[A/G]AGATTCAAAGATTCT	146691
rs763075851	snp	C/G	4.94474e-05	0.00497205	synonymous-codon, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17850929	CTCAATGTCGTCCAT[C/G]ACAGATGGCTGCGCA	146691
rs763102373	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17934527	GATACGGTAACAATG[A/G]CAAACATCTTAGTAG	146691
rs763131283	snp	C/G/T	3.29572e-05	0.00405928	missense, intron-variant	TOM1L2	GRCh38.p7	17:17862827	GAACTGAGGGTGCCA[C/G/T]TGACGCTCTCTGTCC	146691
rs763159614	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17901422	CAGGCAGTGCTCACA[A/G]CCTCGTGATTTGGCC	146691
rs763162352	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17866006	CTCGGCCTCCCATAG[C/T]GCTGGGATTACGGGC	146691
rs763182884	snp	A/G	4.94947e-05	0.00497443	missense, upstream-variant-2KB, intron-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17862738	CCACATACGTCTTGC[A/G]CTGCTCAGCCAAGGA	146691
rs763199988	snp	C/T			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17846142	CGCTGGTCTCTTCTC[C/T]CGTCAAGCCCAGCCC	146691
rs763236649	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17896132	AATTGGCATTCACTC[C/T]CTTGTAGTGATCCAT	146691
rs763254512	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17941911	GAAGGATCCCTTGAG[A/G]CCAGAAGGTCAAGTC	146691
rs763257649	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17947517	TGACCATGTGAGGAC[A/G]CAGCAAGACAGTAGC	146691
rs763303387	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17946338	TCATCATCCTAAAAA[C/T]AAATCCTGTACCTGT	146691
rs763309121	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17959597	CAAACCCCAAGCAAC[A/G]TCATTTCTCAGGCCT	146691
rs763310647	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17954661	TTCCAGAAATTTTCT[C/G]GTAGAGTTGTCCAAA	146691
rs763326982	in-del	-/GGTC			intron-variant	TOM1L2	GRCh38.p7	17:17910353	TCTTGCCTTCCACTG[-/GGTC]GGTCCCCAGTGCCCA	146691
rs763335303	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17923262	AAAAATTAGCCAGGC[A/G]TGGTGGTGGGTGCCT	146691
rs763356707	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17854017	GACTCATTACAATAT[A/G]GAAGCCACTTGGCCT	146691
rs763363266	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17894766	CGAAGCCCTGCGTCT[A/G]CTACAAATACAAAAA	146691
rs763366138	snp	A/G	3.29658e-05	0.00405978	intron-variant	TOM1L2	GRCh38.p7	17:17850866	CGCTCCACACCCCAC[A/G]GATGAAATAGAAAAG	146691
rs763374689	snp	A/T	1.64757e-05	0.00287012	missense, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17884751	ATCAGGACTGCTTCG[A/T]AAGGCATCAGCCCAT	146691
rs763404528	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17955894	AGACCTTCGCGGTGA[A/G]TGTTACAGCTCTTAA	146691
rs763415717	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17907823	TAGGTTTATGAACCC[A/G]TAGAGTCTGGAGCCA	146691
rs763486300	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17883306	TAATTATGCAATTTA[A/C]CAAATGTTTTTTGTA	146691
rs763488691	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17896170	CTGAAATGAACCAGA[A/G]GGGTTCTTTCTGTTC	146691
rs763499038	snp	A/C	1.6623e-05	0.00288292	intron-variant	TOM1L2	GRCh38.p7	17:17898716	ATACTTACAATCCCA[A/C]TTGAGGACACGATCC	146691
rs763566748	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17939225	TGGTGTTGAGACGAA[C/T]ACCAGGCAAAAAGTT	146691
rs763600302	in-del	-/C			intron-variant	TOM1L2	GRCh38.p7	17:17850514	CAAAACAAAACAAAA[-/C]AAAAAACATGCTCCC	146691
rs763600521	snp	C/T			intron-variant, upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17972060	GACGACCAGGATGCC[C/T]AGCCCGCCCGTGAGG	146691
rs763605866	snp	C/T	1.69896e-05	0.00291454	intron-variant	TOM1L2	GRCh38.p7	17:17869328	AAAAAAAAAAAGAAA[C/T]CCGGCTCCCACCTCT	146691
rs763620356	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17854341	GAGCAGGGGGCACTG[C/T]GCTGAGTCTTAGGGG	146691
rs763629822	in-del	-/AT			intron-variant	TOM1L2	GRCh38.p7	17:17931632	CAGAAGACCTTACAC[-/AT]GAGGGGACCTCAAAA	146691
rs763691164	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17937867	CAAATCATAGCTCTT[A/T]AGCTTAAAGACAGCT	146691
rs763737427	snp	C/T	4.9476e-05	0.00497348	synonymous-codon, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17907506	CGTCCAATCCTCACT[C/T]TGCAGGGAGCCATCT	146691
rs763757770	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17951750	TCCATGGGGACGTGG[C/T]GCTTAGGAAGGAAGT	146691
rs763761771	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17944626	CAAAGCACCAGGCAC[A/C]TGCTTCTCTTGTGAA	146691
rs763767594	snp	A/G	1.648e-05	0.0028705	synonymous-codon, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17882762	TGGGGCCTGCGGTGC[A/G]GAGTAGGGAGCAGGA	146691
rs763773589	snp	A/G	1.65053e-05	0.0028727	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17879739	TCACTCCGCAGCCTG[A/G]CAATCTGGTGGGGGC	146691
rs763811929	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17849838	TGAGAGAAGCAATTT[C/T]TTTTCGAGACAGCCC	146691
rs763821451	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17863903	CAGGGTCTCACTCTG[A/G]ATGCCCAAGCTGGAG	146691
rs763886725	snp	A/T			upstream-variant-2KB, intron-variant, utr-variant-5-prime	TOM1L2, DRC3	GRCh38.p7	17:17973092	CTTCTCATTTATAAA[A/T]TGAGCACGTAGGTCC	146691
rs763897661	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17915010	CTTGTAAAGTATAGC[C/T]TTTGTTTGGATGTGT	146691
rs763937698	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17938776	AAAGGGTTTTTTTTT[C/T]TTTTTAATATTTTGT	146691
rs763953806	snp	C/T	1.6486e-05	0.00287102	missense, intron-variant	TOM1L2	GRCh38.p7	17:17862842	CTGACGCTCTCTGTC[C/T]CCAAGTCTGTGGCAA	146691
rs763970351	snp	A/T			upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	TOM1L2, DRC3	GRCh38.p7	17:17972896	TTCCCCTTAGCAACC[A/T]AGTCGCGGCGCTTGG	146691
rs763971752	snp	C/G	1.64876e-05	0.00287116	stop-gained, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17882712	GCAAGTACCTGTTCT[C/G]AATTGGCTGTGATGG	146691
rs763973355	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17867863	ACAGTGGTCTACAAG[G/T]AGAACAGGAATATTA	146691
rs763977896	in-del	-/TTTC			intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17860728	GTGCATTCATACACA[-/TTTC]TTTGTTAGGCAAAAA	146691
rs763997155	in-del	-/A			intron-variant	TOM1L2	GRCh38.p7	17:17869309	CAATCTTTTCAAGGG[-/A]AAAAAAAAAAAAAAG	146691
rs764026015	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17857605	CTTACAGAGATTATG[A/C]AAAAATAGGAGGGGA	146691
rs764054455	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17922585	TCTGGGGACTGGGGG[A/T]CAGTCTTGGCTCTCT	146691
rs764061081	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17864262	GTCACCCAGGCTGGA[A/G]TGTAGTAGAGCGATG	146691
rs764066754	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17953705	TGAGTGGGGGGAGCA[A/C]ATAGGGTGTGTAGTG	146691
rs764083091	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17887030	CAGCTAGAGTGCTCG[A/G]AGGTGCAGGCGTACA	146691
rs764127169	in-del	-/CACC			intron-variant	TOM1L2	GRCh38.p7	17:17935875	ATTTAGCAAATTCTG[-/CACC]AGGAATGACTCACAC	146691
rs764138261	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17876540	CCAGGATCAAAGTTA[C/T]AGGGAGCCACACCTT	146691
rs764155638	snp	C/T	1.6708e-05	0.00289028	intron-variant, synonymous-codon, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17893799	ACAGTTCTTCACACA[C/T]GTCTCCAGCACCTGA	146691
rs764167124	snp	C/T	1.65685e-05	0.00287819	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17869466	GCCCGACAGGTCCTG[C/T]TGAGCTCCTAGGGAA	146691
rs764172507	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17893298	CCCTTACCTTGCTCC[A/G]CCTGACCCAGAGTTG	146691
rs764180348	snp	G/T	1.65671e-05	0.00287807	intron-variant, missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17893701	TGTACAATGGTGGGA[G/T]GGTTGTTCTTGGGAG	146691
rs764189024	snp	C/T	4.11751e-05	0.00453717	synonymous-codon, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17866333	GAGGGAAGATGGGGG[C/T]GCTGTGTTCCCCACC	146691
rs764201570	snp	C/T	8.26084e-05	0.00642631	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17869395	CATGCAGCAGCTCCT[C/T]GGTGACCTCCTCATT	146691
rs764387332	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17932993	TATCAGTTATGATTG[C/T]ATTCAGCTGCAAGCA	146691
rs764412291	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17900329	GTTCAAGACCAGCCT[C/G]GCCAACATGGTGAAA	146691
rs764501922	snp	A/C	3.32508e-05	0.00407729	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17861564	ACCCTGGAGATGAAG[A/C]AGCAGCACAAGCAGA	146691
rs764518109	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17929075	GCACTGCTGTGAGAA[C/T]GGGCCTTTCCTTGGC	146691
rs764523616	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17908833	AACCCCTTTACACTT[C/T]TGATGGAAATGTAAA	146691
rs764537039	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17876096	TTCATTGAAGACAAA[C/G]CTCAAAAGGCTAAAT	146691
rs764549020	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17880038	GTGCACCAAGCTGGC[G/T]CTCCGTCTCGGCTCT	146691
rs764650052	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17907826	GTTTATGAACCCGTA[C/G]AGTCTGGAGCCAAAC	146691
rs764653662	snp	A/G	1.64838e-05	0.00287083	synonymous-codon, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17882726	TGAATTGGCTGTGAT[A/G]GGGCCAGTCACACTC	146691
rs764661705	snp	A/C			intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17858661	GATCTTGGCTCACTG[A/C]AACCTCTACCTCCTG	146691
rs764665585	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17954796	GGCATGACCAAGGGC[C/T]GGACTAAGTTAGAGG	146691
rs764767701	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17867688	TTTTTCCAGCTGGAG[C/T]CTTAGACACCCAGCT	146691
rs764772285	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17949085	CAGGTCAGGGACACC[C/T]TAATTGAGTGTTCTC	146691
rs764778677	snp	A/G	1.69226e-05	0.00290878	intron-variant	TOM1L2	GRCh38.p7	17:17907550	TGAAATCAGAGAGAA[A/G]ATGGGTTTACATTTC	146691
rs764820375	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17903470	CAAAAAAAATTAGCT[A/G]GGCGTGGTGGCGGGC	146691
rs764825094	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17962605	AGGCATGAGCCACCG[C/T]GACTGGCCCAATGTG	146691
rs764829383	snp	C/T			synonymous-codon, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17869393	CACATGCAGCAGCTC[C/T]TCGGTGACCTCCTCA	146691
rs764845408	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17880986	GGTTCCCACTCGCTG[G/T]GCCATCTTCCACTAT	146691
rs764890724	snp	A/C	1.64787e-05	0.00287038	missense, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17882773	GTGCGGAGTAGGGAG[A/C]AGGAGGCGGCGAGGA	146691
rs765019809	snp	A/G	1.68346e-05	0.00290121	intron-variant	TOM1L2	GRCh38.p7	17:17893813	ATGTCTCCAGCACCT[A/G]ATGTGGGGAGGGAAG	146691
rs765044123	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17947244	GCCCATGCTGGTCTT[C/G]AACTCCTGGGCTCAA	146691
rs765045148	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17930081	ATTCCAAAAACAAAA[C/T]AAAAAAGACACTCCA	146691
rs765072717	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17891157	AGGCCCTGTTCTGCT[C/G]AGGTCCCCATGGCCA	146691
rs765104318	snp	A/G	3.32441e-05	0.00407688	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847684	GGCTTCTTCCGGCCA[A/G]AAGGGTTTGAGGCTG	146691
rs765145771	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17875048	GATCACTTGAGGTCA[C/T]GAGTTCAAGACCAGA	146691
rs765161676	snp	C/T			intron-variant, upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17971778	GGAAGGGCTGAGCCT[C/T]GATGGGCAGGGAAGC	146691
rs765177582	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17919012	TTCCCAGCTGTCCCC[A/G]GTTCTCCCTTCAGAC	146691
rs765197663	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17932723	TCCTTGGGCCTCAAT[A/G]TTCTTATCTATAAAA	146691
rs765201504	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17940959	GATGCTTGCAAATCA[C/T]ACTTGTAAGATTTGT	146691
rs765270469	snp	A/G	1.66388e-05	0.00288429	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17861440	TGACTTTCCCTCCAG[A/G]AGACTCCAGGCAGAA	146691
rs765274456	snp	A/G	1.65075e-05	0.00287289	intron-variant	TOM1L2	GRCh38.p7	17:17879607	CACCACAGGCCAAGT[A/G]CTTCTGAAAGATGAC	146691
rs765284245	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17970660	ACACTCTTTTGGGGT[C/T]CCTCATGCATTATAA	146691
rs765327633	snp	A/G	1.66236e-05	0.00288297	intron-variant	TOM1L2	GRCh38.p7	17:17869480	GTTGAGCTCCTAGGG[A/G]ACACATGCACCTCTG	146691
rs765331014	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17910536	TCTACTTTGAATGGT[A/G]TGGGGTGGGATTCAG	146691
rs765383988	snp	A/G	1.64776e-05	0.00287028	intron-variant	TOM1L2	GRCh38.p7	17:17898562	GCAAGGAGTTCCCCA[A/G]ATGACTTCTCTCCTC	146691
rs765444230	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17863721	GCCCAGCTGTTTTAA[A/C]ATTATTTTGTAGAGA	146691
rs765500440	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17944798	CACTTGTGCTCTCCA[C/T]ATTAAATGCTTAGCG	146691
rs765502240	snp	G/T	1.67122e-05	0.00289064	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17861591	CAGAGTTCATTTTCC[G/T]CCAGTGGTCATGGAG	146691
rs765522493	snp	A/G			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17844952	AACACTCACGGAGAG[A/G]CTGGTGGGCCTTGAG	146691
rs765560944	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17966339	GAATAAATAAATGAA[C/G]AAATTCTAAATAATC	146691
rs765565789	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17910933	CCATTCTCACCAAAA[C/G]GATGTTGCTGAATGC	146691
rs765568832	in-del	-/TC			intron-variant	TOM1L2	GRCh38.p7	17:17969862	GAATAGGAATCTTTC[-/TC]TCTCTCTCTCTCTCT	146691
rs765596067	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17851017	GGGGAGACAGAACAC[C/T]GGAACAAAGGAAATC	146691
rs765614583	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17907767	CTGAAAAGCTTATGA[C/T]AGGCCTAAGCCATCA	146691
rs765632307	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17856481	CCTTGCTCCCACGGC[C/T]CTGGGTGATCCTGCA	146691
rs765656492	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17893510	ATTCCAGTGGGATGA[G/T]AATTTTTTTTGAAGT	146691
rs765669626	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17906457	ATCACTCTATTTAAC[A/G]TTGCTAATTCCCAGC	146691
rs765692631	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17940797	CATAATAAGGATTCT[A/G]GATTACAGCCCAAAG	146691
rs765694471	snp	A/C	1.64738e-05	0.00286995	missense, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17884672	ACAGAGCGTCCAAGT[A/C]TGCCATGGGAAATTC	146691
rs765717747	snp	A/G/T	6.5908e-05	0.00574023	intron-variant	TOM1L2	GRCh38.p7	17:17866938	ACCTAACAGGGGAAG[A/G/T]GAAAGCAGAAGTAAG	146691
rs765743563	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17953403	GAAGCAGCAGTTTGG[C/T]TGCTGCAGTATTCCT	146691
rs765784686	snp	A/G	1.64749e-05	0.00287005	synonymous-codon, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17884745	GGTGAGATCAGGACT[A/G]CTTCGAAAGGCATCA	146691
rs765794422	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17921169	CCAACTTATTCTCCT[A/G]TCTGGAGAGCTCAGT	146691
rs765794471	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17876276	ACAGGATGACAAAGA[G/T]AGGCTTAACCACCAG	146691
rs765799706	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17967319	TTCTGGTCAGAATTA[A/G]CTAACTACTCACTGA	146691
rs765841228	snp	C/G	2.32431e-05	0.00340896	synonymous-codon, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17866360	CACCATTGGGCTCAC[C/G]ACGGCTGGAGACCCT	146691
rs765841259	snp	C/G	3.31559e-05	0.00407147	intron-variant	TOM1L2	GRCh38.p7	17:17882883	CATGGCAACAACAAA[C/G]TCCTCTGTTTACCTG	146691
rs765859515	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17962393	TGACACGATCTTAGC[G/T]CACTGCAACCTCCTC	146691
rs765874166	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17952220	TGGCAAAACAAAAGC[A/G]AGCTGTAAAATGAAG	146691
rs765894365	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17885150	TGGAGCCTTGTCAGC[G/T]CAGCAGGGTGCCTGC	146691
rs765910316	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17915702	CTTTAAAAAAATTTA[G/T]GTAGAGATGGGGTCT	146691
rs765929422	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17867599	GAGGTGTGTGTTGGG[G/T]TGGGGCAGAATAGAT	146691
rs765936175	snp	C/T	1.64914e-05	0.00287149	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17879673	TGTCCAGGGACCATT[C/T]CTGTTAACATCTCAG	146691
rs765959123	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17928002	TTATATGATGTCTGG[A/G]ATTTACTGAAAAATA	146691
rs766007361	snp	C/T			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17846138	ATGTCGCTGGTCTCT[C/T]CTCCCGTCAAGCCCA	146691
rs766035170	snp	A/G	1.65225e-05	0.00287419	intron-variant	TOM1L2	GRCh38.p7	17:17848788	CTGCACAGAGGCAAC[A/G]AAAGGGGGCTGTAAG	146691
rs766073094	snp	A/C	0.000126649	0.00795666	intron-variant	TOM1L2	GRCh38.p7	17:17866457	ATAAGCCCCAGAACC[A/C]TGGAGTCAGGCTCTG	146691
rs766079786	snp	A/C	1.64762e-05	0.00287016	intron-variant	TOM1L2	GRCh38.p7	17:17898584	TCTCTCCTCAAGGAG[A/C]ATAGCACTCACTGTT	146691
rs766087661	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17929037	TGCTATGGTTCCTAA[C/T]ACCAAGTCTGAAGAT	146691
rs766120755	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17873610	TACTCCCAGCACCGG[C/T]GGCCTGATGGAAGGG	146691
rs766142664	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17941846	TTTCAGCCTCTAAGC[C/G]AGGCGCAGTGGCATG	146691
rs766164554	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17937483	AAGATCTGTAGCAAA[A/T]GAAGGCTGTCACATA	146691
rs766168764	snp	C/G	1.64925e-05	0.00287158	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17879632	GATGACTCACCTGCA[C/G]CAACTCCAGATCAGA	146691
rs766172203	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17903069	CTCTGTAAGACTCCA[C/G]TCTGGTGTCACTTCC	146691
rs766187358	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17970494	TTTCTGGCTCCCTCC[A/G]TTAACTGGCTGGAAA	146691
rs766193767	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17889320	GCAAAGGTGCCACTG[C/G]GTAGGCTGACCATGC	146691
rs766199692	snp	C/G	1.65228e-05	0.00287422	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847735	GGCGAGGGGAGGTCG[C/G]GAACCATTTCAGCAG	146691
rs766289206	in-del	-/ACTA			intron-variant	TOM1L2	GRCh38.p7	17:17958461	AGTCAAAAACAGGAG[-/ACTA]ACTTTCAAACAATAA	146691
rs766304843	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17848371	GGGAGGCAGGATGTG[A/T]AGGGCAGGGGATGTG	146691
rs766358379	snp	A/G	8.26166e-05	0.00642662	intron-variant	TOM1L2	GRCh38.p7	17:17898691	TGGAAAAAAGAACAG[A/G]CATATAAAGATACTT	146691
rs766375648	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17901837	GCCATTCCCAAATCC[A/G]CAAGCTGTGCCTTGA	146691
rs766396570	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17897776	GCTGGGTAAACCTCC[A/G]GACCTCTCTGAGCCT	146691
rs766406012	snp	A/G			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17845078	AGGACAGGCCATCTC[A/G]CCAGGGCTAAGTGGA	146691
rs766416704	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17930376	AAAAAAAGGGGGGTC[C/T]GGGAATGTGTAGGAC	146691
rs766416833	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17944777	GGCGGGGAAACAGGA[A/G]GTCCGCACTTGTGCT	146691
rs766459285	snp	A/G/T	3.29708e-05	0.00406011	synonymous-codon, upstream-variant-2KB, intron-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17862745	CGTCTTGCGCTGCTC[A/G/T]GCCAAGGAGTTTCCT	146691
rs766461149	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17879851	AATCCTTCTCACTGG[A/G]AGATCTGGGTTGCCT	146691
rs766472530	in-del	-/CT	1.64781e-05	0.00287033	frameshift-variant, upstream-variant-2KB, intron-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17862759	CAGCCAAGGAGTTTC[-/CT]CTCGTCTGGGCAAAC	146691
rs766592157	snp	C/T			intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17860384	GCAGCCAGCTGGCTC[C/T]TCTGCGCCCTCTGGT	146691
rs766612416	in-del	-/A			intron-variant	TOM1L2	GRCh38.p7	17:17962232	AAAATGGTAGTTGCC[-/A]AGGGGCTGGGGGGAG	146691
rs766630564	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17920890	ATCCACCCGCCTCAG[A/C]CTTCAAAGTGCTGGG	146691
rs766643444	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17910209	GACGGGAAACCCGGG[C/G]CCCGCAGAAGAAAAG	146691
rs766740210	snp	A/G	1.8763e-05	0.00306286	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847587	TGCCCGGTGTCCACG[A/G]GGTGCGAGCGGGGAC	146691
rs766745475	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17905187	ATCACCTATATTTAG[C/T]TGGTGAAAATATGCC	146691
rs766766518	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17924232	TATAGAGACAGAAAA[C/T]AGATTAGTGATTGCC	146691
rs766846988	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17952064	TATGCTGTTCCAGTA[C/T]TACTTATAAGGACAA	146691
rs766851403	in-del	-/TCTC			intron-variant	TOM1L2	GRCh38.p7	17:17903161	TAGCTATATATAGCT[-/TCTC]TCTCTCTCCCTGCCC	146691
rs766870008	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17919650	AAGTGGGGCATGGGG[A/G]AGGAGGGGCCACGGT	146691
rs766904000	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17965587	GGGCAGCACAGCGTG[A/T]CAGGATACCAGCTCT	146691
rs766949845	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17899020	AGCACAGGTGCCAGC[A/G]TAGGGAAGAGACTCT	146691
rs766958630	snp	G/T	1.64746e-05	0.00287002	missense, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17884660	TGTGTATGGGAGACA[G/T]AGCGTCCAAGTCTGC	146691
rs766966190	snp	C/G/T	3.29664e-05	0.00405984	intron-variant	TOM1L2	GRCh38.p7	17:17850867	GCTCCACACCCCACA[C/G/T]ATGAAATAGAAAAGT	146691
rs766985318	snp	A/G	1.64765e-05	0.00287019	intron-variant	TOM1L2	GRCh38.p7	17:17866931	CGTTCGAACCTAACA[A/G]GGGAAGGGAAAGCAG	146691
rs766985378	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17924255	TGATTGCCTGGGGTT[A/G]GAAGGGCTGGGGGAA	146691
rs766989418	snp	C/T	1.65135e-05	0.00287341	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847754	CCATTTCAGCAGCTT[C/T]GGCTCTTTCTTCAAG	146691
rs767031647	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17927533	TGGAGCAAATAAACA[C/T]TTGGCCTCGTGAGAA	146691
rs767036101	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17926556	AACAAACAGGGAAGA[C/T]TACATTTAAATGTAA	146691
rs767041568	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17958204	TTCAAAACAAACGAA[C/G]GAACAAACCATGCTC	146691
rs767044612	snp	A/G	1.64779e-05	0.00287031	intron-variant	TOM1L2	GRCh38.p7	17:17866846	TAGGTCTGGCCTCAG[A/G]AGATGACAGGATTCT	146691
rs767047484	snp	A/G	4.96192e-05	0.00498067	synonymous-codon, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17869372	GACGTTGTTGAGGTC[A/G]TCGTTCACATGCAGC	146691
rs767068906	snp	C/G			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17843988	AGACAATGTCTCTGG[C/G]GTGGAAACACTTCTC	146691
rs767100984	snp	C/T			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17844698	AAAGGCCCATGGTGC[C/T]AGGGGCCCAACTGCA	146691
rs767141444	in-del	-/G	0.00394559	0.0442406	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847597	CCACGGGGTGCGAGC[-/G]GGGACCCGCCATCTG	146691
rs767150986	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17857357	CCAAATTCACAGGCA[C/G]TGGGCTACAGAGGGC	146691
rs767218531	snp	A/G	1.65198e-05	0.00287395	intron-variant	TOM1L2	GRCh38.p7	17:17848796	AGGCAACAAAAGGGG[A/G]CTGTAAGGCCACTGG	146691
rs767238338	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17851187	GGCTCCCGGCAGGGC[C/G]GGCGGTAAGGAAGGT	146691
rs767294561	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17953155	GCGTGGTGGTCACAC[A/C]TGTAATCCCAGCTAC	146691
rs767308444	snp	C/T	1.64874e-05	0.00287113	intron-variant	TOM1L2	GRCh38.p7	17:17850851	CAGAAGAGCCTCTGC[C/T]GCTCCACACCCCACA	146691
rs767313526	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17948850	ACACCCAGCCTCCCT[C/T]CTATTGCCTGATGGA	146691
rs767364974	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17960235	AACAATACTAAGCTC[C/T]CTGGTTTAGTGGTTA	146691
rs767376067	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17916583	TCAATTGACCATATA[C/T]GGGAGAGTTTATTTC	146691
rs767382159	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17900597	AAGAAAATTTTAAAA[C/T]ACCCTGAATCACCTG	146691
rs767388904	snp	C/T	3.30071e-05	0.00406232	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17879730	ACGTCCAGTTCACTC[C/T]GCAGCCTGGCAATCT	146691
rs767390778	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17934670	TTTTAAAAATGTGTC[A/G]ACCTATACAGCCATC	146691
rs767441675	snp	C/G	1.65575e-05	0.00287724	intron-variant	TOM1L2	GRCh38.p7	17:17898704	AGACATATAAAGATA[C/G]TTACAATCCCACTTG	146691
rs767454634	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17849914	GGCAGCTGCCTTCTT[C/T]GGCAAGGCATGTGTT	146691
rs767472379	in-del	-/CA			intron-variant	TOM1L2	GRCh38.p7	17:17966715	AGTCTCTTAACTTCT[-/CA]GAGCCTCGATTTCCT	146691
rs767497661	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17946463	AAATGCAATCATACA[A/C]TATATAGCTGTTTGT	146691
rs767508859	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17915434	ATGACTACTGATGTT[A/G]AGCATTTTTTCATGT	146691
rs767545045	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17970374	CAACCACATTTGTAT[A/T]TTAAATCCCCTTTAA	146691
rs767575657	snp	C/T	1.65721e-05	0.0028785	intron-variant, missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17893693	CTTTGTCCTGTACAA[C/T]GGTGGGAGGGTTGTT	146691
rs767580290	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17955974	CTCCCAATGGGTTCG[C/T]GGTCTGCGCCAGCCT	146691
rs767581425	snp	A/G	3.30136e-05	0.00406273	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847591	CGGTGTCCACGGGGT[A/G]CGAGCGGGGACCCGC	146691
rs767644184	snp	A/G			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17846400	ACCAGGGCCTGGGAT[A/G]ACCCGAGTCCCTTGC	146691
rs767644230	snp	C/G			intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17860020	TGGGCTCAGACCCAG[C/G]CCTGGGCGCTGATAA	146691
rs767724052	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17886453	TGCCCGTAGGGAGTG[C/T]CTCTGGCCCCGCCCC	146691
rs767751728	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17931265	TTCCCCAATTCTCCA[A/G]TCAAAAGAGGTCTCA	146691
rs767761596	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17963876	TAGTTGATTGCAGGA[C/T]ACCGTGCTAGGGATT	146691
rs767781016	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17923398	AAGAGTGAAACTCCA[C/T]CTCAAACAACAACAA	146691
rs767812363	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17968956	GTTTCTGACTCCTTC[A/G]GCACTTACAATCTAC	146691
rs767898569	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17918297	TTTTCTACATGTAAA[A/G]TCATGTCATCAGGGA	146691
rs767898853	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17907045	GGACCTCCCTCCATG[A/G]ACACGGTGGTGCTCT	146691
rs767900512	snp	C/T	1.65463e-05	0.00287626	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17869454	CGCTGCTGCATGGCC[C/T]GACAGGTCCTGTTGA	146691
rs767906568	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17922830	AGCGGGGAAGCAGAA[A/G]GGGAGGGTGACTGTC	146691
rs767946263	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17896273	TGGGGTCAAGGCAGA[C/T]GGCAAGAAGTATGCT	146691
rs767967807	snp	A/G	1.64849e-05	0.00287092	synonymous-codon, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17850947	AGATGGCTGCGCAAC[A/G]GGGATCTATGGAGGC	146691
rs767978741	snp	A/T			intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17858243	TTTTTTTTTCTCTTT[A/T]CTAGTGGCATGTGTA	146691
rs767981068	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17857235	TGGGATTACAGGCGT[A/G]AGCCACTGCACCCGG	146691
rs768028583	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17943436	CTGCTGCCTGGAGAG[C/T]GCAGAAAAGGCCTCA	146691
rs768031165	in-del	-/T			intron-variant	TOM1L2	GRCh38.p7	17:17873959	TTATTTACTTACTTA[-/T]TTTTTTTTTTTTTTA	146691
rs768031454	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17930279	CATACAAACTTTAGC[C/T]CATTCTCCTAACAAA	146691
rs768052391	in-del	-/A			intron-variant	TOM1L2	GRCh38.p7	17:17906131	TTGTCTTCTCTTTTC[-/A]ATTTTTTTTTTTTTT	146691
rs768074715	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17921863	AGGGGCTGTTCCCCT[C/T]GCCCTCGTGCCCACC	146691
rs768108957	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17910059	TTGAATGGTTAAAAT[A/G]ATAAATTTAATGTTA	146691
rs768126093	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17933746	ACAAGTCACCCAGAA[A/C]ACCCACTCGTTTGTT	146691
rs768193109	snp	A/G	0.000331066	0.0128617	synonymous-codon, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17869360	GTATCGAAGGAAGAC[A/G]TTGTTGAGGTCATCG	146691
rs768202695	snp	G/T	0.000574988	0.0169459	intron-variant, downstream-variant-500B	TOM1L2, LOC100507131	GRCh38.p7	17:17857758	GCTTGGCTCGGCTGG[G/T]GACTCCTCACCATTC	146691
rs768213281	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17853242	CATCTCCAGAGAGAA[A/C]ATAGTCCCACACTAG	146691
rs768253550	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17968057	AGTGTTCTACTAAAT[C/T]GTACCAGGTTAGAAT	146691
rs768256975	snp	C/G	1.65184e-05	0.00287384	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17869423	ATTGGACACGCGGGA[C/G]ATGAGCTCCACGATG	146691
rs768263789	snp	C/T	3.31384e-05	0.00407039	intron-variant, missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17893744	CCAGAACACTGTCGA[C/T]GAAATCTCGGTTGGC	146691
rs768289539	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17880536	CACAGGGACCTTCCT[A/T]GCCCACAGTGAAATA	146691
rs768296193	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17884912	AAACCTATTCTGTTC[C/T]TCTCCTTCCGCAACT	146691
rs768297194	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17920712	CGATCTCGGCTCACT[A/G]AAACCTCTGCCTCCT	146691
rs768306290	in-del	-/ATT			intron-variant	TOM1L2	GRCh38.p7	17:17903993	ACTCAGGAAGAGATT[-/ATT]ATTATTATTATTATT	146691
rs768347011	snp	C/T	1.65002e-05	0.00287225	intron-variant	TOM1L2	GRCh38.p7	17:17850986	GCGGGCCAGGCAGCC[C/T]CCACACAGCCAGCGA	146691
rs768356880	snp	C/T	0.00010869	0.0073711	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	TOM1L2, DRC3	GRCh38.p7	17:17972337	GACAACACGCAGCGG[C/T]CCGGGCCCCCTGTCT	146691
rs768416256	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17903380	TGTAATCCCAGCACT[C/T]TGGGAGGCTGAGGCG	146691
rs768423724	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17932342	GGTACTTTGCCCAGG[A/T]TGGTCTCAAACTCCT	146691
rs768436115	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17866018	TAGTGCTGGGATTAC[A/G]GGCGTGAGCCACTGC	146691
rs768465150	snp	A/G			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17844539	TTCCCTCTAGCCCAG[A/G]CCAGCAACAACCCCT	146691
rs768530732	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17856895	TACATGAGAACCAAC[C/T]GTGTTTACAACATTG	146691
rs768532380	snp	C/T			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17845427	GGCTCCCCAGGAGGG[C/T]GCCTATTTCAGCTTC	146691
rs768540767	in-del	-/AGTC			intron-variant	TOM1L2	GRCh38.p7	17:17930485	CACTTGGGGCTCCTA[-/AGTC]TGACTTATTCCACAT	146691
rs768544792	snp	C/G			upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	TOM1L2, DRC3	GRCh38.p7	17:17973935	CCCCAGCTCCAACCT[C/G]TCTGGTCTTCAACAA	146691
rs768569904	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17959741	CTCAAAGACAGCCCA[A/G]TTCTCTGAGATGAAA	146691
rs768573380	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17933536	TCTTTCCCTTGACCC[C/T]CATCAATCCTGGCCT	146691
rs768626903	snp	C/T	1.65081e-05	0.00287293	intron-variant	TOM1L2	GRCh38.p7	17:17884599	TCACCCGTTCTGCAG[C/T]AGGTCTTTCTAGAAA	146691
rs768643173	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17894615	TCCCTTGCAAGATTG[C/T]TGGAAAGATTAGCAA	146691
rs768645207	in-del	-/AA			intron-variant	TOM1L2	GRCh38.p7	17:17900195	TCCAGCCTGGGCGAC[-/AA]GAGTGAAACTTCATC	146691
rs768681187	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17853372	AGCTACAACAAAGAC[A/G]TTAAGGGGTCAGGGG	146691
rs768704936	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17894407	TGTTCAATTCAGACC[C/T]TGCCTGCTCCTCCCT	146691
rs768728978	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17848753	GGCTCCAAGATGATG[G/T]GGGCTGGCTCCTGTG	146691
rs768730361	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17888783	CCATTTCCGCTCCTG[A/G]AAACAATTTCAAGGG	146691
rs768745604	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17901447	TTGGCCTCTGGGCCA[C/T]GATCAGGCTCCTCAA	146691
rs768756002	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17907210	TTCCACTTGTGATTA[A/G]AAGCAGGTGATTAAA	146691
rs768768771	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17851943	AAAAGGTTTAAGTTG[C/T]CATCAAATATGACAT	146691
rs768807403	snp	A/C/G	3.30585e-05	0.00406551	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847726	TCCATGGGGGGCGAG[A/C/G]GGAGGTCGGGAACCA	146691
rs768809501	snp	A/C/T	6.5895e-05	0.00573967	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17866896	TACTGGCATTTTGAA[A/C/T]GGATCGGCCAGACCT	146691
rs768833972	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17949760	AGGCAGAAGAGCACT[C/T]CTCAGAGAGTGGCCT	146691
rs768852539	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17917313	CACTCCAGCCTGGGC[G/T]ACAGAGCAAGACCCC	146691
rs768864554	snp	A/G	3.52964e-05	0.00420083	intron-variant	TOM1L2	GRCh38.p7	17:17866430	AGTACCTGTCAGAAC[A/G]TGAGATTGGCCATAA	146691
rs768903930	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17916451	TCATTTTTGCATATG[A/G]TATAAGATAATGGTC	146691
rs768907659	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17929458	CCAACGTGGAGAAAC[C/G]CCATCTCTACTAAAA	146691
rs768962757	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17948665	TCAAAAAAAAAAGGT[A/G]GCCCTTTCTTAGAGT	146691
rs768975586	in-del	-/CT			intron-variant	TOM1L2	GRCh38.p7	17:17851906	CCTCAGGGACAGAGA[-/CT]CTGAAAAATGCACAT	146691
rs768983782	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17923379	GCATTCCAGTCTGGG[C/T]GACAAGAGTGAAACT	146691
rs768984648	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17924102	AGATCGCGCCACTGC[A/G]CTCCAGAATGGGCAA	146691
rs768989569	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17914360	CAGTCTTTTCTTCTC[C/T]AAACAGATGTGCCTA	146691
rs768989668	snp	A/C	1.64923e-05	0.00287156	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17879695	ACATCTCAGACATGA[A/C]TTTTGTGTTTCCTCG	146691
rs769004751	in-del	-/CATGC			intron-variant, upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17971434	GGGAGGCACTGCAGG[-/CATGC]CATCCCCCTGCCAAG	146691
rs769013577	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17961391	GGGATACATGGGGAG[A/G]CCTTGCCACTACAAA	146691
rs769040668	snp	A/C	1.65315e-05	0.00287498	intron-variant	TOM1L2	GRCh38.p7	17:17879591	ACGGTGGAAGAGCTG[A/C]CACCACAGGCCAAGT	146691
rs769041760	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17890337	ACACCCCGGTATGAG[A/G]TGGATACATATGAAA	146691
rs769042139	snp	C/G	1.65201e-05	0.00287398	intron-variant	TOM1L2	GRCh38.p7	17:17847816	GCAAGGGTCAGGGTT[C/G]GTGAGGGCAGGCCAC	146691
rs769042756	snp	C/T	4.94197e-05	0.00497066	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17898636	TAGTTCCGGTTCCCG[C/T]TGAGCCGCTTCTTCA	146691
rs769048052	in-del	-/G			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17844749	CCCAGTGGCCAAAAA[-/G]GTAGGCAGGAGGGAA	146691
rs769071002	snp	C/G			intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17860954	CCTGGCTCTCGAGTG[C/G]CTTCTAATGGGGTTG	146691
rs769083500	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17940788	TCTGCTTTCCATAAT[A/G]AGGATTCTGGATTAC	146691
rs769102232	snp	A/C			intron-variant, upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17971092	GTCCCCAGGTGTCCA[A/C]ATCCCCCCTATAGGA	146691
rs769111096	snp	A/G	1.65119e-05	0.00287327	missense, upstream-variant-2KB, intron-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17862731	AGGGGCCCCACATAC[A/G]TCTTGCGCTGCTCAG	146691
rs769113196	in-del	-/A			intron-variant	TOM1L2	GRCh38.p7	17:17954835	ACTAAGAGCAAACAC[-/A]TGCTAAACACATTAT	146691
rs769160652	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17875790	AAGTTTGAAGGAACA[C/G]GGAATAAGGTCCTGA	146691
rs769180874	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17964576	TTTCATATTTTCTAT[C/T]GGTTATACATCGTTT	146691
rs769193463	in-del	-/T	1.65082e-05	0.00287295	intron-variant	TOM1L2	GRCh38.p7	17:17848808	GGGCTGTAAGGCCAC[-/T]TGGCCAGGCCATACC	146691
rs769223608	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17849099	CATGTTTTAGGTTTT[G/T]ATCCTCCAGAAAGGC	146691
rs769247640	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17897598	TCTTTTTAAATTCTC[C/T]GACAGCTTTGGTAAG	146691
rs769266819	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17945253	AGAGCCAAATGTTTC[A/G]CCACACACACACATA	146691
rs769270179	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17923275	GCGTGGTGGTGGGTG[C/T]CTGTAATCCCAGCTA	146691
rs769302557	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17883101	GAATGTGTGGCAGAC[C/T]AATGAAAGCAACTCC	146691
rs769317296	in-del	-/TGT			intron-variant	TOM1L2	GRCh38.p7	17:17954976	CTCCGTTTCTTTTGC[-/TGT]TGTTGCTCACCCTAG	146691
rs769354989	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17937313	AACACCGACATTTTT[A/G]TTTTTATCTTTGATC	146691
rs769430448	snp	C/G	1.65323e-05	0.00287505	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17869443	GCTCCACGATGCGCT[C/G]CTGCATGGCCCGACA	146691
rs769449870	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17962209	TAGTCAAATTCATAG[C/T]GACAAAGTAAAATGG	146691
rs769453331	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17932112	TACTTACCAGCTATA[C/T]GTCTTCCACACTCAT	146691
rs769476296	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17885437	AGTTCACCCCCAGGG[G/T]TCCTTTTCCCAGACC	146691
rs769479302	snp	C/G			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17844888	GTGCTTATAAGGAAT[C/G]CCAGCAATAATTTAG	146691
rs769482159	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17897223	TATTGAAAGCCACTC[A/G]TTTTGGGCATCACTC	146691
rs769503926	snp	A/G	1.64866e-05	0.00287106	missense, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17882844	GGCATGGTCGCAGCT[A/G]GATCCACTTCAGGGA	146691
rs769508253	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17931213	CTACCTATTTTTACC[C/T]ATCCTATCCTCTTTA	146691
rs769532771	in-del	-/T			intron-variant	TOM1L2	GRCh38.p7	17:17930936	TTTTTTCCCTAACAG[-/T]TAAGTTTTGAGATTT	146691
rs769533678	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17910623	TGTGCAGGCTGGAGC[A/G]CAATGGTGTGATCTC	146691
rs769547330	in-del	-/ACAGACATACAC/ACAT			intron-variant	TOM1L2	GRCh38.p7	17:17894946	AAAACATACATACAT[-/ACAGACATACAC/ACAT]ACATACATACATACA	146691
rs769550289	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17944553	CACAAGACAAACTAA[C/T]GCAGACCATCTGCTC	146691
rs769606765	snp	C/T	3.30535e-05	0.00406518	missense, upstream-variant-2KB, intron-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17861495	TCTGAACTCTGTTTT[C/T]GATTGTCTAGTGCAG	146691
rs769681432	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17952907	CACACTTCCTCCTCC[A/G]CTGCCCTGACAGAAC	146691
rs769735536	snp	C/T	1.64784e-05	0.00287035	synonymous-codon, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17898671	TCGAATGGCATCCTT[C/T]GGCCTGGAAAAAAGA	146691
rs769753139	snp	C/T			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17843523	TAATTTGTTCAATTA[C/T]TTATTTATTGTGGAG	146691
rs769753590	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17905727	GTTTTCTGCATTGTC[C/G]TTGGCCTGCCCCCAG	146691
rs769772666	snp	A/T	0.000119083	0.0077154	intron-variant	TOM1L2	GRCh38.p7	17:17869230	TGAGTATTTTCCAAC[A/T]CTAATCTCTCTCCCT	146691
rs769784423	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17966377	TAGCCTGTCCACAAG[A/G]AAACCTACATTTAAT	146691
rs769797815	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17908778	CTACTATCAAAAAAA[G/T]AGAAAATAACAAGTG	146691
rs769833356	snp	A/G	1.64741e-05	0.00286998	stop-gained, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17866902	CATTTTGAACGGATC[A/G]GCCAGACCTGTATCG	146691
rs769844824	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17855549	CCCTGAGAGCCGCCC[A/G]GCCCTAGCCCATTGA	146691
rs769848024	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17914510	GAAAAGGGCAGAGAG[C/G]GGGTATGGCATCTCT	146691
rs769913914	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17865661	TGGGATTACGCGCCC[A/G]GCCTTGACCTAGTTA	146691
rs769922740	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17906419	CAGATGTGACCCACC[C/G]AGCCCAGCCAAGACT	146691
rs769961716	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17961281	AAAAAAATGAACCAA[A/G]TGCAGGGGTTCACGT	146691
rs769973265	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17927305	CAGCACAGCTGGGTT[C/T]ACCATGTGAGTAACG	146691
rs770006780	snp	A/G	1.65307e-05	0.0028749	intron-variant	TOM1L2	GRCh38.p7	17:17848775	GCTCCTGTGCAGCCT[A/G]CACAGAGGCAACAAA	146691
rs770014925	in-del	-/AAGG			intron-variant	TOM1L2	GRCh38.p7	17:17926864	CTCTGTCTCAAAAAA[-/AAGG]AAGAAAGAAAAAGAA	146691
rs770023091	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17900063	CTGAAATATACAAAA[A/C]TTAGCTGGGTGTGGT	146691
rs770046435	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17954638	ATCATTCTAAAGGAG[A/G]TGGGGAGTTCCAGAA	146691
rs770065822	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17872972	GGAAACAGATCCAAG[C/T]TACCCTCCAGAAGAC	146691
rs770071204	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17927236	AGTCCAAAGGGACAG[A/G]CCCGACATTATTTTC	146691
rs770102493	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17968523	TACAAAAATTAGCCC[G/T]GCACGGTGCCAGGCA	146691
rs770109067	snp	A/G	1.65946e-05	0.00288046	intron-variant	TOM1L2	GRCh38.p7	17:17907439	CCAGGAGAGGGGGGC[A/G]CACGTACCCTTCCTC	146691
rs770131170	in-del	-/GCA	2.58896e-05	0.0035978	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17862429	GGCAGGGTGGTGTCT[-/GCA]GCAGCAGCAGCAGCA	146691
rs770137220	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17945549	TCTTAGGGAGACCCA[C/G]ATTACATAGGATGAA	146691
rs770144279	snp	C/G			upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	TOM1L2, DRC3	GRCh38.p7	17:17973878	ATCTGTTATCTGTGA[C/G]GAGGCCACTCCGTTG	146691
rs770145206	snp	A/C	1.65745e-05	0.00287871	intron-variant	TOM1L2	GRCh38.p7	17:17879795	AGGTCAGTCAGCCTG[A/C]ACTTGCAATATCAGA	146691
rs770151031	snp	A/C/T	4.9504e-05	0.00497493	missense, upstream-variant-2KB, intron-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17862737	CCCACATACGTCTTG[A/C/T]GCTGCTCAGCCAAGG	146691
rs770178685	in-del	-/AGGAAGGAAAGC	1.65166e-05	0.00287368	intron-variant	TOM1L2	GRCh38.p7	17:17879759	CTGGTGGGGGCCACG[-/AGGAAGGAAAGC]AGGAAGGAAAGGTCA	146691
rs770219168	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17851833	AGCTTCCAGGCATAC[C/T]AAGGTGTACCACGGG	146691
rs770259852	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17948503	AATACAAAACAAAAA[G/T]CAGCCAGGTATGGTG	146691
rs770272217	in-del	-/CCTG			intron-variant	TOM1L2	GRCh38.p7	17:17852786	GGAGAATCACTTGAA[-/CCTG]CCTGGGAGGCAGAGG	146691
rs770291890	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17888495	AGGGAGCTTCTGTCA[A/G]CTCCTGCTTATGCCC	146691
rs770296627	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17881986	CCCCCAAGTCTGACC[A/G]ATTCTCAAATTGTAA	146691
rs770319721	snp	A/G	1.73222e-05	0.00294292	synonymous-codon, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847644	AGCTGCTCACAGGGC[A/G]AAGAGGGCATCCTCT	146691
rs770324932	snp	C/T	1.6582e-05	0.00287936	intron-variant	TOM1L2	GRCh38.p7	17:17862895	AGAACAAAATGTAGA[C/T]TGTAGATCTGATGAA	146691
rs770350098	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17897072	CCTGCTAGAGGAAGG[C/T]AAGTAAACGCAGAGT	146691
rs770391284	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17869685	ACTTTTTCAGCAGAC[A/G]AATGTCCAGACATAC	146691
rs770395178	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17944015	TCTGCCCCTCTCAGT[A/G]CATGCTGCTACATTA	146691
rs770469338	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17901378	TGGCATCAAGCCCTA[C/G]CAGCTTTCAGGGGAA	146691
rs770481247	snp	A/G	3.29832e-05	0.00406085	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17879676	CCAGGGACCATTTCT[A/G]TTAACATCTCAGACA	146691
rs770518778	snp	C/T	1.65932e-05	0.00288034	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17862711	ATCTTTAGAGAGCCA[C/T]TAAAAGGGGCCCCAC	146691
rs770540822	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17929833	CTCAGTCAGATACCA[C/T]TTCTGCCCTAGAGCT	146691
rs770540968	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17944450	ACACCGACAGCTTGA[C/T]GCTCCCTTCACCTCC	146691
rs770554022	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17909523	AGATGATTCTACTTA[C/T]AATCAGGTACCTAGA	146691
rs770586024	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17909159	GCATTCCAACCCGGG[C/T]GACAGAGCCAGACTC	146691
rs770602040	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17895938	GCAGCCAGCCAGAAT[C/T]GTTCCTTGCCTTGCT	146691
rs770606864	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17923972	GAAACCCCGTCTCCA[C/T]TAAAAAAATACAAAA	146691
rs770625527	snp	C/G	3.29527e-05	0.00405898	missense, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17884642	AGCTTACCCGCTGTG[C/G]TGTGTGTATGGGAGA	146691
rs770662248	snp	A/G	2.70852e-05	0.00367993	intron-variant	TOM1L2	GRCh38.p7	17:17869275	TTTGTTTATGAAAGA[A/G]ATCCCTCTGTTATGG	146691
rs770663633	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17943034	AGTGGGAGGGGAGGA[G/T]GATTAGATGAAACAA	146691
rs770677720	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17964897	AACAGAGCAGGAGGA[A/G]GAGCAGGCTGACGCC	146691
rs770678264	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17951487	TTTGAGTTTGTGCAT[A/T]AAAAGTTGCTGCCCT	146691
rs770717113	snp	A/C	1.64741e-05	0.00286998	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17866916	CGGCCAGACCTGTAT[A/C]GTTCGAACCTAACAG	146691
rs770803074	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17964467	ATGAAGAGTGAAATA[C/G]AAAAGTATTCCATTA	146691
rs770812967	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17855326	TGAGGAGGGAGTCCC[A/G]CCCTCCAAACCCAAG	146691
rs770819502	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17953449	CAAGCAGGAGTGCCC[C/T]GGATCACTTTCCCCA	146691
rs770842618	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17917851	TTTCATCTACTCAGG[A/T]GGCTAAGGTGGGAGG	146691
rs770847198	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17919009	CGGTTCCCAGCTGTC[C/G]CCGGTTCTCCCTTCA	146691
rs770851384	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17950363	AGGGTTTTACCAAGT[C/T]GGCCGCGCTTGTCTC	146691
rs770856083	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17963443	AAAACGCTGGAGCTA[A/G]AGCCCCTGGCTGGAG	146691
rs770869564	snp	A/C	8.243e-05	0.00641936	missense, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17882842	TGGGCATGGTCGCAG[A/C]TGGATCCACTTCAGG	146691
rs770898804	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17853667	AGCCCTAGAGGGCAC[A/G]CTGAGGAGAGTGCAC	146691
rs770932579	snp	C/G	3.2962e-05	0.00405954	missense, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17850898	CGAGTCTCACCAGGT[C/G]GGTCCTGAGCCACAC	146691
rs770939105	snp	A/G	1.65307e-05	0.0028749	intron-variant	TOM1L2	GRCh38.p7	17:17848908	ACTGGTCCAAGCACT[A/G]CCCGCCCAGCCACCT	146691
rs770971613	in-del	-/A			intron-variant	TOM1L2	GRCh38.p7	17:17896894	AGTGACTAAGAGAGT[-/A]AAGTGAAGCCCTATC	146691
rs770976138	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17863498	CTCACAGGAAAAAAT[G/T]TGTGGAGGAAGTGGC	146691
rs770988131	snp	A/C			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17844499	GCGCTAATAGAAAGA[A/C]AGGAGGACAGACGGA	146691
rs771011577	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17877480	CTTTCTAAGCAGACA[C/G]TGGTATTTCTCCACA	146691
rs771044361	in-del	-/T	0.00025083	0.0111961	intron-variant	TOM1L2	GRCh38.p7	17:17893657	GCAAGGGGTCCAACC[-/T]TACCTGGATCAGAGC	146691
rs771067229	snp	A/C			intron-variant, upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17971533	CTCAAATTAGCAAGT[A/C]CCGGAGCAGGGGGCA	146691
rs771071673	snp	C/G			downstream-variant-500B	TOM1L2	GRCh38.p7	17:17843057	AGTCTACCTGGCTTG[C/G]AGCAGCAGTTCTCAA	146691
rs771105975	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17905671	AGCCTCGTACAGTGC[C/T]GGGATTGCAGGTGCA	146691
rs771115076	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17940027	GTGAAACCTCATCTC[C/T]ACTAAAAATACAAAA	146691
rs771122365	in-del	-/T			intron-variant	TOM1L2	GRCh38.p7	17:17920335	CGCTAATGTTCAATA[-/T]TTTTTTTTTTTTTTT	146691
rs771136426	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17893058	ATAATGAACATTTTC[C/T]GTTTGAAGGTATGTT	146691
rs771142793	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17871632	GCAGAGATTGCACTA[A/C]TGCACTCCAGCCTGG	146691
rs771160539	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17910846	AGTGCTGGGATTACA[A/G]GCGTGAGCCACTGTG	146691
rs771164302	snp	A/G	3.30338e-05	0.00406397	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17907456	ACGTACCCTTCCTCC[A/G]TCTCATTGATGATGT	146691
rs771193467	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17890755	GTGTGGTCATATTCT[A/G]TTTCTAGATGCAGGG	146691
rs771204409	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17885077	CCTAAAAAGCAGGAA[C/T]TTCCCTAATGGCAAG	146691
rs771240659	snp	A/G	1.7129e-05	0.00292647	synonymous-codon, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847650	TCACAGGGCGAAGAG[A/G]GCATCCTCTGACCGC	146691
rs771276499	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17886559	GCATTTTAGTTTAGG[G/T]TGTTGACTTTAGGGT	146691
rs771291457	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17857709	AGAGGAAGACATGAG[C/T]TGTTACACAGGTAGG	146691
rs771331114	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17865376	ATCTGCCCTCCTTGA[C/T]CTAGTTAATATTTAT	146691
rs771387359	snp	C/T	1.65825e-05	0.00287941	intron-variant, missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17893680	ATCAGAGCAAGCACT[C/T]TGTCCTGTACAATGG	146691
rs771387673	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17947009	GGATTACAGGCGTAC[A/G]CCACCGTGCCAGCCT	146691
rs771396440	snp	C/T	1.6591e-05	0.00288015	intron-variant, missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17893768	GGTTGGCCACAAGGA[C/T]GTGGAAGCGGTGGCC	146691
rs771411240	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17886108	AGTCTGTCATTGTCA[C/G]AGAATTTAACTGTCT	146691
rs771429950	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17901342	GAAAGGATCAGGAAG[A/G]ATCAGTGGCCTGTGT	146691
rs771449834	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17941770	CCATGCCTCACTAAC[G/T]CGGCTGACTGAAAAA	146691
rs771458119	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17849340	CCAATAGCTGGAAAC[C/T]GCATGAGGCCTTGAT	146691
rs771505899	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17923034	GGCCTCAAAGAGTGA[C/T]TACAAAATTCCACAC	146691
rs771517270	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17908660	TCCAAAGAAGATATA[C/T]AAATGACTAACAAGT	146691
rs771620846	snp	C/T			intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17858346	TCTCACTGTGTTGCC[C/T]GGACTGGTCTCAAAA	146691
rs771657492	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17923123	ACAGTGTTGGCTGGG[C/T]GCAGTGGCTCACGCC	146691
rs771680754	snp	A/C	0.000164938	0.00907973	intron-variant	TOM1L2	GRCh38.p7	17:17884802	TGTTAGGAAGCATTT[A/C]TCAGAGCTGCCATGG	146691
rs771693513	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17911597	CATTGAGTGGCCTTA[A/G]TTCCAGAGGCAATCA	146691
rs771724120	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17872846	CAGCAAGCCCTGGCT[C/G]TCCTTGGCTGGGGAG	146691
rs771735894	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17963280	CTAAGTGCTGGAAGA[C/G]AACAAAGAGAGAGCA	146691
rs771771905	snp	C/T	2.05675e-05	0.00320676	intron-variant	TOM1L2	GRCh38.p7	17:17869302	ATGGCAACAATCTTT[C/T]CAAGGGAAAAAAAAA	146691
rs771778314	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17940318	TAGCAAGAGTAATCA[A/G]TAATTGGTAGCTTTA	146691
rs771799911	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17954520	GTTTCGCCATGTTGG[C/T]CAGGCTAGTCTCGAA	146691
rs771808887	snp	C/G	1.64808e-05	0.00287057	missense, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17850908	CAGGTCGGTCCTGAG[C/G]CACACCTCAATGTCG	146691
rs771826244	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17922317	CTCGGTGAAGGGGAG[C/T]GGTGAGAGGAGGCCA	146691
rs771922193	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17867499	TCCTCTGCACCCAGT[C/T]AGGCAGTGCAGGGGG	146691
rs771924095	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17930169	TGAGACAGCCTCTTT[C/T]TGTTGGACTGGAATG	146691
rs771960708	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17928874	ATCAGAGAACAATGC[C/T]TCCATTTCTGATTCA	146691
rs771961539	snp	A/G	1.64868e-05	0.00287109	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17907483	ATGTCACAGATCTCC[A/G]TATTCAACGTCCAAT	146691
rs771977467	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17929534	TACTCAGGAGGCCGA[A/G]GCAGGAGAATCGCTT	146691
rs772001738	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17962082	CAATAGAGATGAAAC[C/T]TGAAGACATTATGCA	146691
rs772011316	snp	C/T			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847243	AATGCCTGAGAAGGT[C/T]GCTGAGCCAGGCAGA	146691
rs772024120	snp	A/G	1.97963e-05	0.00314607	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17866307	TCACCTAAGCCTGCA[A/G]GCTGGGAGGAGAGGG	146691
rs772037979	snp	C/T	4.94841e-05	0.00497389	intron-variant	TOM1L2	GRCh38.p7	17:17850972	GGAGGCGGCAAGCAG[C/T]GGGCCAGGCAGCCCC	146691
rs772076266	snp	C/G	5.7784e-05	0.00537482	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	TOM1L2, DRC3	GRCh38.p7	17:17972314	CAGGAGGAACTCCAT[C/G]TTGGGTGGACAACAC	146691
rs772118140	in-del	-/A			intron-variant	TOM1L2	GRCh38.p7	17:17949417	CAACTGGGTCAGGAG[-/A]ATAAATGTTACAAAG	146691
rs772133243	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17880691	CAACATCCAGAGCCG[G/T]ACCTGAGCCTCTCTG	146691
rs772168419	snp	C/T			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17846850	AGCCTGCAGTGTGTG[C/T]GTGGCAGTTTGGTTT	146691
rs772175200	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17889105	GCCGACTGAGCCCTC[A/G]CACATGTTGGTAAAA	146691
rs772186384	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17895743	AGCAGCCACATCAGC[C/T]AAGAGTGCCTCAGAT	146691
rs772198251	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17890550	GTAAATAAACTGTAG[C/T]GTGTTCACACAACAG	146691
rs772227609	in-del	-/AG	1.67234e-05	0.00289161	intron-variant	TOM1L2	GRCh38.p7	17:17907542	CTTTTCTGTGAAATC[-/AG]AGAGAAAATGGGTTT	146691
rs772235089	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17854793	CCCAGCTTGGCCTCC[C/T]AAAGTGCTGGGATTA	146691
rs772252818	snp	A/G	1.68071e-05	0.00289884	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847664	GGGCATCCTCTGACC[A/G]CTCTGGCTTCTTCCG	146691
rs772255966	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17938492	TGACTACCAGGAGAG[A/G]CACTGGGGAGGAATA	146691
rs772296196	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17951148	GTCAATCAGCCTCAT[C/T]CATAAATCCTAGATG	146691
rs772296884	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17923144	GGCTCACGCCTGTAA[C/T]CCCAGCACTTTGGAA	146691
rs772301870	snp	A/G	1.73372e-05	0.0029442	intron-variant	TOM1L2	GRCh38.p7	17:17893857	CCAGTGGGAGCTGGA[A/G]AAGACACTGGGAACT	146691
rs772321781	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17902892	ATAGGTATTATTGGC[A/G]ACCCCATTTTATAAG	146691
rs772321994	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17918829	AAGTATCTTCTTGGC[C/T]CCCAACCCCAACCTA	146691
rs772354264	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17937421	CACACCTGGGTCCCA[A/T]CAGGCTCGGATTAGG	146691
rs772391750	in-del	-/C			intron-variant	TOM1L2	GRCh38.p7	17:17865742	TGGCAGGTGACCTTT[-/C]TTTTTTTTTTTTTTT	146691
rs772399187	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17937258	ATGAATTCCCTCCTC[C/T]GGTTTTGTAACAAGC	146691
rs772402961	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17967750	GTAGCTGGGATTATA[C/T]GCGCGTGCCACCATG	146691
rs772403465	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17910747	GCTAATTTTTGTATT[C/T]GTAGTAGAGATGGGT	146691
rs772474503	snp	C/T			upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17972515	TATTGGTCGTTACAC[C/T]TCTGTCAGCAAAGCC	146691
rs772504166	snp	C/G/T	0.000115752	0.00760683	synonymous-codon, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847722	AGCCTCCATGGGGGG[C/G/T]GAGGGGAGGTCGGGA	146691
rs772516795	snp	A/G	1.66112e-05	0.00288189	intron-variant, missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17893777	CAAGGATGTGGAAGC[A/G]GTGGCCACAGTTCTT	146691
rs772518636	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17914043	AGGCCCGCAGGCAAA[C/G]CTGCTTCCATCAGGA	146691
rs772519751	snp	G/T	1.65384e-05	0.00287557	intron-variant	TOM1L2	GRCh38.p7	17:17879578	CCTCCAACAGTGTAC[G/T]GTGGAAGAGCTGCCA	146691
rs772531326	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17956971	CCAGAGAAGGCATCG[A/G]GGCTGAGGAGGCGCC	146691
rs772614418	snp	C/T			intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17859966	CTAGTCCAAGCCACA[C/T]ACACAAAGGGTGAAG	146691
rs772700157	snp	C/G			intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17861721	GGGCTCATGTTGTCT[C/G]TCTCCCTGCAGTGGA	146691
rs772719061	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17928972	CTAGATCCTTGCTGG[A/T]CCACACAGAAAAATC	146691
rs772725338	snp	A/G			upstream-variant-2KB, intron-variant	TOM1L2, DRC3	GRCh38.p7	17:17974048	GGCCCTGAACCCAGG[A/G]CAACTGTGAGAAACA	146691
rs772742687	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17889698	TTTCCATAATGGAAA[A/G]GTTAAGGCTGTACCC	146691
rs772743120	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17925229	TTTATGGCAATGCAA[A/G]AACAACCTAATACAG	146691
rs772748379	snp	A/G	3.29728e-05	0.00406021	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17907492	ATCTCCATATTCAAC[A/G]TCCAATCCTCACTTT	146691
rs772749418	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17895792	GATTTATTGTTCCCC[C/T]CTTTGGTCCTTGAAA	146691
rs772790024	in-del	-/AGAA			upstream-variant-2KB, intron-variant	TOM1L2, DRC3	GRCh38.p7	17:17973270	CCAGCCTCCTTTCAT[-/AGAA]AGAGAGGTACCCGGT	146691
rs772799062	snp	A/C	3.29848e-05	0.00406095	missense, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17882850	GTCGCAGCTGGATCC[A/C]CTTCAGGGACACTCT	146691
rs772805848	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17872924	CACAAGGCACAGGAC[A/G]TGCAAGTCAGGGGAG	146691
rs772828407	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17923553	TAATTAGCTGGGCGC[A/G]GTGGTGAGCATCTGT	146691
rs772840957	snp	A/G	1.65252e-05	0.00287443	missense, upstream-variant-2KB, intron-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17861507	TTTCGATTGTCTAGT[A/G]CAGAAGCAAGTCCTC	146691
rs772874374	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17908664	AAGAAGATATATAAA[C/T]GACTAACAAGTATGT	146691
rs772877503	snp	C/T			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847320	TGGAGGAAAGACAGT[C/T]CGGGTGGTCTGCTCA	146691
rs772890967	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17857385	GGCTTCCCTGACTGG[G/T]CAGATGCTTTGAGTC	146691
rs772892360	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17934372	GTATCACTTGAGCCC[A/G]GGGATCAAGGCTGCA	146691
rs772921498	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17941804	AAATCCACAGATAAC[C/T]TATGAACCTCATTTT	146691
rs772956323	snp	C/G	0.00021486	0.0103626	intron-variant	TOM1L2	GRCh38.p7	17:17848778	CCTGTGCAGCCTGCA[C/G]AGAGGCAACAAAAGG	146691
rs772974977	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17875243	CCTGGGTGACAAAGC[A/G]AGACTCCTTCTCAAA	146691
rs773003515	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17962097	TTGAAGACATTATGC[A/T]AGTGAAGTCAGTCAT	146691
rs773005336	snp	C/T	4.94336e-05	0.00497135	intron-variant	TOM1L2	GRCh38.p7	17:17898567	GAGTTCCCCAGATGA[C/T]TTCTCTCCTCAAGGA	146691
rs773028858	snp	C/G/T	3.29567e-05	0.00405924	missense, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17884635	AGCTGGAAGCTTACC[C/G/T]GCTGTGGTGTGTGTA	146691
rs773045572	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17963380	GCTCCTTCTTGTCCA[A/G]ATGGAAACAGACCAT	146691
rs773052629	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17929562	CTTGAACCCGGGAAG[C/T]GGAGGTTGTGGTGAG	146691
rs773084795	snp	A/C/T			intron-variant	TOM1L2	GRCh38.p7	17:17936499	AAGGAATTTATTATA[A/C/T]GTAAATAATCTGAAA	146691
rs773094679	in-del	-/TAA			intron-variant	TOM1L2	GRCh38.p7	17:17883478	GGTGGCTTACGCCTG[-/TAA]TCTCAGCACTTTGGG	146691
rs773096067	snp	C/T	1.65638e-05	0.00287778	intron-variant	TOM1L2	GRCh38.p7	17:17866450	ATTGGCCATAAGCCC[C/T]AGAACCCTGGAGTCA	146691
rs773111864	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17944332	AGGCAGCCTTGCTGC[A/G]GTGCCCTTCATGAGT	146691
rs773142860	snp	C/T			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17844977	CTTGAGAGTCCAGGT[C/T]TCCTGACAGAGCCGC	146691
rs773144616	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17876168	TAAAGATCCCAGAAA[A/G]CCAAACTCAGGCTTT	146691
rs773147713	in-del	-/A			intron-variant	TOM1L2	GRCh38.p7	17:17869784	TTGCTTTTTCTCAAC[-/A]AAATATTCCAGACAC	146691
rs773152958	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17910066	GTTAAAATGATAAAT[G/T]TAATGTTATGTGTAT	146691
rs773154426	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17868947	AAATCCTTTTTCTTA[C/T]TAGAGATTTTTTTTC	146691
rs773213119	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17956528	GGCGGTCGATGGGAC[C/T]GGGCGCAGTGGAGCA	146691
rs773226131	snp	A/G			intron-variant, upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17971380	TGATTCCCAGTCCAG[A/G]GCTCTTATCATTAAA	146691
rs773232917	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17916830	GAGTTTGACACCAGT[A/C]TGGTCAACACAGTGA	146691
rs773242434	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17867566	CTCCTGTCAGGTGGG[A/G]AACGGAAGAGTAGTT	146691
rs773262232	snp	G/T	1.66225e-05	0.00288287	intron-variant	TOM1L2	GRCh38.p7	17:17882664	AAAGATGAAAAAGGA[G/T]AGTCAGCTGGCTTGC	146691
rs773340889	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17880730	TTTCCTCACCTACAG[A/G]AAGGTGGCACTAACC	146691
rs773352083	in-del	-/C	3.32557e-05	0.00407759	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17862698	CAATCCCCCCAATAT[-/C]TTTAGAGAGCCACTA	146691
rs773409145	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17941004	CAATCTTCTGCTAAA[A/G]TCTGTTCTAGTGTTT	146691
rs773414221	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17925568	AGGTATAGCCCAGGC[A/G]CAGTGGCTCATGCCT	146691
rs773435585	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17932360	GTCTCAAACTCCTGG[A/C]CTCAAGCAATCCTCC	146691
rs773440286	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17904697	GAGAATGCAGCACCT[A/G]ACCTTGACTACCTTT	146691
rs773440314	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17889222	CAGAAAGCCCCCATA[C/T]GGGAAAGGAAGGAGT	146691
rs773446024	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17874808	GGCCTCTATGCTCCA[A/G]TCCTGGAGAAGCATC	146691
rs773465702	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17924192	TATGATTCCATTTAT[A/C]TAAAATGTCCAGAAT	146691
rs773493334	snp	C/T	1.64958e-05	0.00287187	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17879713	TTGTGTTTCCTCGAA[C/T]GACGTCCAGTTCACT	146691
rs773534509	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17853813	AAGCCTTAGAGATTT[G/T]GGTGGAGAGGCAGGA	146691
rs773538313	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17883434	GATGAAAACAGCCTC[C/T]AGAAAGGGCAATCCC	146691
rs773560651	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17958276	CACAGCAAATCAGCA[A/G]CAGAGCAGTGAACAG	146691
rs773562974	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17885700	GAGGCCGAGGCGGAC[A/G]GATCACGAGGTCAGG	146691
rs773580157	in-del	-/A			intron-variant	TOM1L2	GRCh38.p7	17:17910105	CCACCACCAAAAAAG[-/A]CAGAAAAATTATACA	146691
rs773608074	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17945771	CCATTTAAAAAAAGA[A/G]AAAAAGTAATTATAG	146691
rs773614320	snp	G/T	4.94311e-05	0.00497123	missense, intron-variant	TOM1L2	GRCh38.p7	17:17862821	TGGAGTGAACTGAGG[G/T]TGCCACTGACGCTCT	146691
rs773629735	snp	A/G			intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17862212	CTCAAAACATGTACA[A/G]TGCCTCCCTGAGATG	146691
rs773666865	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17931309	CCCATGCCTCTGCAC[G/T]GCCAAGCAAGGCAGA	146691
rs773672073	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17965189	CCCTACCTCTGTAAT[C/G]ATATTCATGCTTCCA	146691
rs773723970	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17898826	ACTGAATGTCCATCA[A/G]TACACAACAGGTTAA	146691
rs773730802	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17944694	GTATAAAACCAACGT[C/G]TCCTACAAGGAGAGG	146691
rs773786811	snp	G/T	1.65641e-05	0.00287781	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17862718	GAGAGCCACTAAAAG[G/T]GGCCCCACATACGTC	146691
rs773805032	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17848318	GAGAGGAGGACAGGA[A/G]CACGGAGAGGCAGAT	146691
rs773831819	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17856121	ACCACCAGCTGCCAA[A/G]GCCACCCTCAGGGGA	146691
rs773854749	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17940504	GACTCTGGCATGCCA[C/T]AGCCAGGAGAGAGTC	146691
rs773860151	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17910766	GTAGAGATGGGTTTC[A/G]GCACGTTGGCCAGAC	146691
rs773862235	snp	A/G	1.64751e-05	0.00287007	stop-gained, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17884750	GATCAGGACTGCTTC[A/G]AAAGGCATCAGCCCA	146691
rs773863712	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17857287	TTCAAATCATTTTGA[C/T]GGACTTAGTGGATAT	146691
rs773934143	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17885006	ACAAAACTTAATTTA[G/T]CATGTATTTCCTTGG	146691
rs773951337	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17871528	ATACAAAAATAAATT[C/G]GGCACAGTGGCATGC	146691
rs773951419	snp	C/T	3.29484e-05	0.00405871	synonymous-codon, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17866918	GCCAGACCTGTATCG[C/T]TCGAACCTAACAGGG	146691
rs773961319	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17921948	TGTGCCACACTGTCA[C/T]CAGCCTTTTTTTTGA	146691
rs773981773	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17953047	TCATTTGGGAGGCTG[A/T]GGTGGGCAGATCACT	146691
rs774005970	snp	A/G	1.6476e-05	0.00287014	missense, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17884648	CCCGCTGTGGTGTGT[A/G]TATGGGAGACAGAGC	146691
rs774015131	snp	A/G	1.64727e-05	0.00286986	synonymous-codon, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17884730	TATGTGCACAACGCC[A/G]GTGAGATCAGGACTG	146691
rs774037815	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17870764	CATAAACTCTTGAGG[A/G]GGTGTTACCATTTAT	146691
rs774055848	in-del	-/TT			intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17858237	TACATTTTTTTTTTC[-/TT]TCTTTTCTAGTGGCA	146691
rs774072940	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17959841	AGACTACAAGGCTTA[C/T]GCTTCATTAATGATT	146691
rs774084956	in-del	-/A			intron-variant	TOM1L2	GRCh38.p7	17:17906888	GGAAGAAGTACAAAT[-/A]AGAGTGCAGCTGTAA	146691
rs774120020	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17879209	CCTGCAAAATGTGAT[C/G]TTGAGGGACCAAAAT	146691
rs774126086	snp	C/G			upstream-variant-2KB, intron-variant	TOM1L2, DRC3	GRCh38.p7	17:17973988	GGGGACCCAGGTTGG[C/G]TGGTAAACTATAAGA	146691
rs774127424	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17966627	AGTGCAAAAAGTAAC[A/C]TAAATGGCAGCACAG	146691
rs774128533	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17916496	TGCATGTGGATATTC[A/C]GTTTTCCCAGCACCA	146691
rs774131488	in-del	-/AG			upstream-variant-2KB, intron-variant	TOM1L2, DRC3	GRCh38.p7	17:17974297	GTCATCTCTCACCTC[-/AG]TACTTTTGCAATTCT	146691
rs774179630	snp	A/T	4.65864e-05	0.00482608	intron-variant	TOM1L2	GRCh38.p7	17:17869285	AAAGAAATCCCTCTG[A/T]TATGGCAACAATCTT	146691
rs774180023	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17915183	TTATTAAAATAGTGG[C/T]GATGGTATCCTTTCA	146691
rs774249640	snp	A/G	0.000115646	0.00760327	intron-variant	TOM1L2	GRCh38.p7	17:17848792	ACAGAGGCAACAAAA[A/G]GGGGCTGTAAGGCCA	146691
rs774279637	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17923350	AGGTTGCAGTGAGCC[A/G]AGATCGCGCCACTGC	146691
rs774304707	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17927434	CATCTCTTTCTGAGG[C/T]CAGGACCTGCATGCA	146691
rs774378173	in-del	-/AG	1.68213e-05	0.00290006	intron-variant	TOM1L2	GRCh38.p7	17:17907413	GGCCCCTAAAAGCTC[-/AG]AGAGGCTTCCCAGGA	146691
rs774380990	snp	A/G	1.64958e-05	0.00287187	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17907468	TCCGTCTCATTGATG[A/G]TGTCACAGATCTCCA	146691
rs774389722	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17902782	AAAGTGAAATAGTAC[A/T]TCCACATAGATATAG	146691
rs774432293	snp	A/G	1.65318e-05	0.002875	intron-variant	TOM1L2	GRCh38.p7	17:17898695	AAAAAGAACAGACAT[A/G]TAAAGATACTTACAA	146691
rs774472699	snp	C/T	3.29592e-05	0.00405938	missense, intron-variant	TOM1L2	GRCh38.p7	17:17862831	TGAGGGTGCCACTGA[C/T]GCTCTCTGTCCCCAA	146691
rs774487903	snp	A/C/G	7.49702e-05	0.00612214	utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847589	CCCGGTGTCCACGGG[A/C/G]TGCGAGCGGGGACCC	146691
rs774525826	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17944610	TTGGAGTTATTCTCC[C/T]CAAAGCACCAGGCAC	146691
rs774529386	snp	C/T	1.65416e-05	0.00287586	intron-variant	TOM1L2	GRCh38.p7	17:17882687	TGGCTTGCCTATGGC[C/T]CCGAAGTATGCAAGT	146691
rs774558994	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17921016	TAACTGAACTCCAGA[C/T]GTTATTTGGATTTCT	146691
rs774590511	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17887041	CTCGGAGGTGCAGGC[A/G]TACAGGAGAGGATTT	146691
rs774592316	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17851121	AACACAGGGCAGCCA[C/T]GTGTGAGATGGCAGG	146691
rs774592333	in-del	-/AG	4.94258e-05	0.00497096	intron-variant	TOM1L2	GRCh38.p7	17:17866930	TCGTTCGAACCTAAC[-/AG]GGGAAGGGAAAGCAG	146691
rs774612139	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17917893	CCGGGAGGTCAAGGC[C/T]GCACTGAGCCGTAAT	146691
rs774642358	snp	C/T	1.65822e-05	0.00287938	intron-variant, missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17893681	TCAGAGCAAGCACTT[C/T]GTCCTGTACAATGGT	146691
rs774645677	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17901534	CTGTCATCCCTCCAG[C/T]CACAGCCTTTGTATC	146691
rs774663891	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17897270	TGTGGCTCAAATTCT[A/G]AGAAAAAATAAAATA	146691
rs774716816	snp	G/T	1.69568e-05	0.00291172	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847657	GCGAAGAGGGCATCC[G/T]CTGACCGCTCTGGCT	146691
rs774721688	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17935632	AGGGACCCAGGGCAA[A/G]TCACCTCCTCCCTGG	146691
rs774723592	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17930102	AGACACTCCATTCTA[A/G]TTCTTCAGAAATGAG	146691
rs774740888	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17948786	GTGCCCAGAGCAAGG[C/T]AGGGGTCCTAGGAAG	146691
rs774776691	snp	C/G			intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17859668	GGCAGAGTGCCTGAG[C/G]TCAGGAGTTCGAGAC	146691
rs774819294	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17958989	TCCAAGTTGAACACA[C/T]AAAGGTGCTGGGAGG	146691
rs774848252	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17943268	CCAATCCACTGTAAC[A/T]GTCACTTTAAAAAAC	146691
rs774925810	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17924155	CAAAAACAAAAACAA[A/G]GGTAAAAATGACTAC	146691
rs774932395	snp	C/G	1.64741e-05	0.00286998	missense, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17884741	CGCCGGTGAGATCAG[C/G]ACTGCTTCGAAAGGC	146691
rs774933868	snp	G/T	1.66043e-05	0.00288129	intron-variant, synonymous-codon, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17893775	CACAAGGATGTGGAA[G/T]CGGTGGCCACAGTTC	146691
rs774935203	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17875791	AGTTTGAAGGAACAC[A/G]GAATAAGGTCCTGAA	146691
rs774957842	snp	A/G	1.65411e-05	0.00287581	synonymous-codon, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17869450	GATGCGCTGCTGCAT[A/G]GCCCGACAGGTCCTG	146691
rs774963184	in-del	-/TCC			intron-variant	TOM1L2	GRCh38.p7	17:17868658	TGTGCTTGCCATTAT[-/TCC]TCCTATTTAAAACTA	146691
rs774969443	snp	A/G	5.17996e-05	0.00508892	intron-variant	TOM1L2	GRCh38.p7	17:17869520	CTGGGTGTGCTTTTC[A/G]TCACATTCTATCTCC	146691
rs774973270	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17963644	GCCAGGAAATGATGG[C/G]TAGTAATGTTAGCTT	146691
rs774999748	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17951670	TACAGGGCAAGGGGA[C/G]GCCAAGGATGCAGGA	146691
rs775006135	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17911606	GCCTTAGTTCCAGAG[A/G]CAATCAGATCCAACT	146691
rs775020276	snp	C/T	4.11599e-05	0.00453633	intron-variant	TOM1L2	GRCh38.p7	17:17869303	TGGCAACAATCTTTT[C/T]AAGGGAAAAAAAAAA	146691
rs775053984	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17883334	GTAATTATAGGAACA[A/T]CAACACTGCTCTCTG	146691
rs775067664	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17848239	ACTGAGAGCTAGGGA[C/G]CAGGGTCCTCTGAAG	146691
rs775083326	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17870542	CCACCTACCTGGGCA[C/T]TGGAGGGTGCCAGTG	146691
rs775117811	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17932124	ATATGTCTTCCACAC[C/T]CATAAAACAACCATA	146691
rs775133629	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17920112	CTGATTTTTAGGTGA[A/C]GTCTAAAGACCCTCC	146691
rs775139589	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17849979	CAGCCAGAGGCCCCA[A/G]CCTGAGGCCTGCTGT	146691
rs775176915	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17882254	ACAACTCAGCTGCAC[A/G]TCTATGCTTTTGGCC	146691
rs775210022	in-del	-/T			intron-variant	TOM1L2	GRCh38.p7	17:17875820	AAGATCTGTTTTCTG[-/T]TGCTGCAAAGATGGG	146691
rs775292981	snp	A/G	3.86593e-05	0.00439638	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	TOM1L2, DRC3	GRCh38.p7	17:17972317	GAGGAACTCCATCTT[A/G]GGTGGACAACACGCA	146691
rs775306249	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17940131	CCAGGAGGCGGAGGT[C/T]GCAGTGAGCTGAGAT	146691
rs775313323	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17952923	CTGCCCTGACAGAAC[A/T]GGAAGGTTGAAAAGG	146691
rs775314255	snp	C/T	4.94442e-05	0.00497188	missense, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17850922	GCCACACCTCAATGT[C/T]GTCCATGACAGATGG	146691
rs775331072	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17894397	TTAATGTCCATGTTC[A/T]ATTCAGACCCTGCCT	146691
rs775383481	snp	C/T			upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant	TOM1L2, DRC3	GRCh38.p7	17:17973889	GTGAGGAGGCCACTC[C/T]GTTGACAGTTGTGTA	146691
rs775385204	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17957764	ACGTACACACACATA[C/T]GATTCATAGGTATGT	146691
rs775432751	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17939050	GCAGCTACTCAGTAA[C/T]GGGATGAAAAGGATA	146691
rs775438283	snp	C/G			upstream-variant-2KB, nc-transcript-variant	TOM1L2, DRC3	GRCh38.p7	17:17972766	CGCCCATAGAAAGTA[C/G]TGATTGGAGAAACAT	146691
rs775497234	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17947445	TGGAGACAGGGTCTT[C/T]AAAGAAGTGATTAAG	146691
rs775513473	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17849414	TAGGTACTTTGGGAG[C/T]GGAGGCTGTGCCTCC	146691
rs775517972	snp	C/G			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17843549	TGGAGTATTTTACAT[C/G]CAAGAACCCAATTAG	146691
rs775520074	snp	A/C/T	3.29599e-05	0.00405944	missense, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17882761	CTGGGGCCTGCGGTG[A/C/T]GGAGTAGGGAGCAGG	146691
rs775523599	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17916364	AGGCATGAATCACCG[C/T]GCCCGGCCTATTTTA	146691
rs775529259	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17927618	TTATGATATTAAGGA[G/T]TATGATTAATTTATT	146691
rs775581607	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17905847	TGAAGCCAGAGTTGC[C/T]CTGGTTCTACATGGC	146691
rs775584579	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17948577	GAATGACTTGAACCC[A/G]GGAGGTGGAGGTTGC	146691
rs775631393	snp	A/C	1.66868e-05	0.00288845	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847674	TGACCGCTCTGGCTT[A/C]TTCCGGCCAGAAGGG	146691
rs775641202	snp	C/G	1.66142e-05	0.00288216	intron-variant, missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17893778	AAGGATGTGGAAGCG[C/G]TGGCCACAGTTCTTC	146691
rs775645193	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17866003	CACCTCGGCCTCCCA[C/T]AGTGCTGGGATTACG	146691
rs775679440	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17885203	CCCTGAAAGCTTCTA[C/T]TGGTGGAGTTGGGAA	146691
rs775685610	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17956215	ACAGAGACCTGATTG[A/G]CCTATTTTGACAGGG	146691
rs775698263	snp	A/T	3.13809e-05	0.00396099	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17866412	TCTTCGGTTACTTCA[A/T]TCAGTACCTGTCAGA	146691
rs775704130	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17889949	ACTTAGCTGAACCTC[C/T]TCTCAGCCTAGCCGC	146691
rs775706872	snp	C/T			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17844847	TTGACAAAATAAATA[C/T]TTTAACCTATAATCA	146691
rs775731394	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17863788	ACCTGGCCTCAAGTG[A/G]TCTTCCCACCTCGGC	146691
rs775753326	snp	A/G	4.08038e-05	0.00451666	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17866329	AGGAGAGGGAAGATG[A/G]GGGCGCTGTGTTCCC	146691
rs775756759	snp	A/G	4.96438e-05	0.00498191	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17869455	GCTGCTGCATGGCCC[A/G]ACAGGTCCTGTTGAG	146691
rs775773355	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17969841	ATTTAAACTACATTA[C/T]TCTGTGAATAGGAAT	146691
rs775780909	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17914633	ACTGCTTCTGTAACT[G/T]CCAGCCTGGTGCCAT	146691
rs775878441	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17923256	ATACAAAAAAATTAG[C/T]CAGGCGTGGTGGTGG	146691
rs775899124	snp	A/G	4.94434e-05	0.00497184	intron-variant	TOM1L2	GRCh38.p7	17:17898546	GGGGGCAAGGCCAGG[A/G]GCAAGGAGTTCCCCA	146691
rs775926878	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17941850	AGCCTCTAAGCCAGG[C/T]GCAGTGGCATGCACC	146691
rs775981133	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17954659	AGTTCCAGAAATTTT[C/G]TGGTAGAGTTGTCCA	146691
rs775982045	snp	A/T	0.00018558	0.00963098	intron-variant, missense, downstream-variant-500B	TOM1L2, LOC100507131	GRCh38.p7	17:17857780	TCACCATTCCTTGGG[A/T]TATAAGCCAGCTGTC	146691
rs775992105	snp	A/G	1.6483e-05	0.00287076	missense, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17850937	CGTCCATGACAGATG[A/G]CTGCGCAACGGGGAT	146691
rs776013093	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17922478	GTAGTGGAGTGGAGA[A/G]ACTGCAGGCAGGAAG	146691
rs776013226	in-del	-/CATTA			intron-variant	TOM1L2	GRCh38.p7	17:17943100	GGGTACACAGAGGTT[-/CATTA]CACTGTTCTCCCAAT	146691
rs776040142	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17851862	GGGTTGCCTGAGCAG[C/T]CACCTTGCTTGGGCC	146691
rs776041143	in-del	-/A			intron-variant	TOM1L2	GRCh38.p7	17:17928159	ATTTTCTGTAACAAC[-/A]AAAAAAAATCAGTAG	146691
rs776070227	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17872979	GATCCAAGTTACCCT[C/G]CAGAAGACTGGGGTA	146691
rs776074804	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17963514	GTTTCTGAACCCCTT[C/T]AAGTCTCTATTTCTT	146691
rs776078170	snp	A/G			synonymous-codon, intron-variant	TOM1L2	GRCh38.p7	17:17862847	GCTCTCTGTCCCCAA[A/G]TCTGTGGCAACAAAA	146691
rs776079260	snp	A/G	3.30726e-05	0.00406635	intron-variant	TOM1L2	GRCh38.p7	17:17879581	CCAACAGTGTACGGT[A/G]GAAGAGCTGCCACCA	146691
rs776087817	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17853265	CACACTAGCGGTTAG[A/C]GTGTGCACCAGCCCT	146691
rs776099677	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17935842	TGAAAATTTAAGTGA[A/C]ATGCACTTCCACCTA	146691
rs776159693	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17896112	GATTCTGGTAACCGT[A/G]AGGTAATTGGCATTC	146691
rs776182476	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17882056	CAATTCATCTAAAAA[A/C]TCCAGTGTGGGGTTA	146691
rs776195752	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17917992	TGAACACAGGATGTT[C/T]TTCCATATATTTATG	146691
rs776217378	snp	A/T			intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17859730	TAGTAAAAACACAAA[A/T]ATTAGCCGGCTGTGG	146691
rs776279483	snp	A/G	3.30087e-05	0.00406242	intron-variant	TOM1L2	GRCh38.p7	17:17850991	CCAGGCAGCCCCCAC[A/G]CAGCCAGCGAGGGGA	146691
rs776288895	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17872748	TGATGAGCAAAAGGA[G/T]CTCAAGTCCCAGCTC	146691
rs776306143	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17897175	CAGTAAAATTCCCTG[A/G]TATATTAGAGCTCAT	146691
rs776317860	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17929943	AGTGAGGTACTACAG[A/T]GAGTGAGTGACAGCT	146691
rs776322417	snp	C/G	0.000108915	0.00737872	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	TOM1L2, DRC3	GRCh38.p7	17:17972340	AACACGCAGCGGCCC[C/G]GGCCCCCTGTCTGCC	146691
rs776341945	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17906344	GTGTTGCCCAGGCTG[C/G]TCTCGAATTCCTGGG	146691
rs776385948	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17870429	GGATGCTACAGAGGA[A/G]GGAGCTGGCAACACT	146691
rs776398222	in-del	-/TTTCT			intron-variant	TOM1L2	GRCh38.p7	17:17865160	GTGGAAAGTGGTGAG[-/TTTCT]TTTAAGTTCCAGACA	146691
rs776411611	snp	C/T			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17846139	TGTCGCTGGTCTCTT[C/T]TCCCGTCAAGCCCAG	146691
rs776427516	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17938713	TTATAATATCCTACA[A/T]GCCTTAACTCATTAC	146691
rs776440985	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17955965	TGTTCATTCCTCCCA[A/G]TGGGTTCGTGGTCTG	146691
rs776443471	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17943110	AGGTTCATTACACTG[C/T]TCTCCCAATTCATAT	146691
rs776443509	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17956082	TTTGTTTCAAAGAGC[A/C]AAAGAACAAAGCCTC	146691
rs776451196	snp	A/G	1.64844e-05	0.00287087	missense, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17882838	GACCTGGGCATGGTC[A/G]CAGCTGGATCCACTT	146691
rs776515059	snp	C/T			intron-variant, upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17971636	ATCCCACAAAGGGTT[C/T]GGGAGAACTGGGTCC	146691
rs776559462	snp	C/T	1.64806e-05	0.00287054	missense, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17882766	GCCTGCGGTGCGGAG[C/T]AGGGAGCAGGAGGCG	146691
rs776751795	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17869114	CTTACAAAGGGCAGA[A/G]CCTAATTCTGCACGT	146691
rs776785602	snp	A/G	1.65195e-05	0.00287393	intron-variant	TOM1L2	GRCh38.p7	17:17879596	GGAAGAGCTGCCACC[A/G]CAGGCCAAGTGCTTC	146691
rs776816714	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17968396	TTTGGGCCGGGCGCA[A/G]TGGCTCACTCCTATA	146691
rs776823842	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17894761	CACGGCGAAGCCCTG[A/C]GTCTACTACAAATAC	146691
rs776836153	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17886752	ATAAAGATGAAAGAA[C/T]TATGGCTCTTCTCTC	146691
rs776837035	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17966240	ATCTATCCAATCTTG[A/C]AACTACTTTCTATCT	146691
rs776844460	snp	A/G	1.65247e-05	0.00287438	intron-variant	TOM1L2	GRCh38.p7	17:17847826	GGGTTGGTGAGGGCA[A/G]GCCACCAGAGGAAGC	146691
rs776846516	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17899074	GTAACTGTGGCTGCC[C/T]CTAAGGAAGGGAACC	146691
rs776850129	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17914357	CCTCAGTCTTTTCTT[A/C]TCTAAACAGATGTGC	146691
rs776879417	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17956574	TGGGGAGGTTCGGGC[C/T]GCATAGGAGCCCACG	146691
rs776896305	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17893059	TAATGAACATTTTCC[A/G]TTTGAAGGTATGTTT	146691
rs776900861	snp	A/C	1.66457e-05	0.00288489	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17861574	TGAAGAAGCAGCACA[A/C]GCAGAGTTCATTTTC	146691
rs776905706	in-del	-/AA			intron-variant	TOM1L2	GRCh38.p7	17:17908316	TACTCCAAATGGATC[-/AA]AGACATAAATGTAAG	146691
rs776946786	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17926090	GTGAGAGGATCACTT[A/G]AGCACAGGATGTCGA	146691
rs776958861	snp	G/T			upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17972619	CACCTCCCCTGGCCC[G/T]CCCCCAAAGGGGAAG	146691
rs776970099	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17879289	TCAGAAAGAAAATAC[A/G]TCAAAGCACCTACAG	146691
rs776971318	snp	C/T			downstream-variant-500B	TOM1L2	GRCh38.p7	17:17843181	GTGGCTCAGGCCTGC[C/T]TGCTCAAGGCCTGGG	146691
rs776971832	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17916453	ATTTTTGCATATGGT[A/G]TAAGATAATGGTCCG	146691
rs777017061	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17934176	GGCATGGTAGCCATT[C/T]TCAAAGTGCTCCAAT	146691
rs777022972	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17920983	AAAACTAAAAAGTTA[A/G]CATTGGTATAGTACT	146691
rs777024931	snp	C/T	1.64933e-05	0.00287165	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17879698	TCTCAGACATGACTT[C/T]TGTGTTTCCTCGAAC	146691
rs777032334	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17863224	CTATTTATTCAGCAA[A/G]TATTTCTTAGGTACC	146691
rs777040845	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17871671	GTGAGACCCTGTCTC[C/T]AAAAAATAAAAATAA	146691
rs777071178	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17953164	TCACACCTGTAATCC[C/G]AGCTACTTAGGAGGC	146691
rs777072681	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17849341	CAATAGCTGGAAACC[A/G]CATGAGGCCTTGATG	146691
rs777087311	in-del	-/C	1.64942e-05	0.00287173	intron-variant	TOM1L2	GRCh38.p7	17:17850969	TATGGAGGCGGCAAG[-/C]AGCGGGCCAGGCAGC	146691
rs777114761	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17967099	GTCCCTCTAGAGAAC[C/G]CTAATACACATAGCA	146691
rs777119567	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17909422	TTCAGCCTTAAAAAG[G/T]AAGGAAATCCTATTG	146691
rs777143699	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17932657	TACTTTGGAACCAGA[C/G]AGAACTACATGCAAA	146691
rs777157335	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17885128	TTCAGCTGCAGGGAG[A/T]GGAAGCTGGAGCCTT	146691
rs777173833	snp	A/G	3.29489e-05	0.00405874	synonymous-codon, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17884661	GTGTATGGGAGACAG[A/G]GCGTCCAAGTCTGCC	146691
rs777176892	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17875415	GCTCACTTGGGAGAC[G/T]TTCCTCTGCTTCCTC	146691
rs777213681	snp	C/G			intron-variant, upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17970777	AAGGCTGGAAAGTAA[C/G]CTAAAATTTCATAAG	146691
rs777229693	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17924630	TTAGCCAGGCATGGT[A/G]GTACATGCCTGTAGT	146691
rs777229886	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17890054	GTCTCATGGTGGGAG[C/G]AGCACTTTCTCTCCT	146691
rs777253791	snp	C/G			intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17861878	CCCTAATACTCCTCA[C/G]AGGGAAGACTAGATA	146691
rs777259902	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17931917	ACATTAATATAACCC[A/G]AGGTGGCCACCTTAC	146691
rs777272185	snp	A/G			intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17859450	CATGGCTTGGGATGG[A/G]ACAAGGTAACCTGAA	146691
rs777316694	in-del	-/A			intron-variant	TOM1L2	GRCh38.p7	17:17958090	GCAAGACTCTGTCTC[-/A]AAAAAAAAAAAAAGA	146691
rs777341786	snp	A/G			intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17859570	ATGGCATTGCCCCAT[A/G]GAGCAGCAAACATGA	146691
rs777359917	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17956243	GGGTGCTGATTGGTG[C/T]GTTTACAATCCCTGA	146691
rs777360187	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17923903	AGCACTTTGGGAGGT[C/T]GAGGTGGGCAGATCA	146691
rs777374433	in-del	-/TTTTTTTTTTTTTT			intron-variant	TOM1L2	GRCh38.p7	17:17917451	AAAATACCATTGGTC[-/TTTTTTTTTTTTTT]TTTTTTTTTTTTTTT	146691
rs777385731	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17964310	GGTCAAGAGCAACAA[C/T]CCCTAACTGATGCTC	146691
rs777391955	snp	C/G	1.64732e-05	0.0028699	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17898618	GCCAGCATCACCTCT[C/G]TGTAGTTCCGGTTCC	146691
rs777403780	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17937124	TGCAGCCCCAAAGGA[C/T]AAAGGAGAGCAATGC	146691
rs777409996	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17923135	GGGCGCAGTGGCTCA[C/T]GCCTGTAATCCCAGC	146691
rs777423892	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17874201	CCTCATGATCTGCCC[A/G]CCTTAGCCTCCCAAA	146691
rs777440568	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17893341	TGACCTCACCAAACC[C/T]GCACGTAGCTCTAAC	146691
rs777473851	snp	A/T	1.75047e-05	0.00295839	intron-variant	TOM1L2	GRCh38.p7	17:17869525	TGTGCTTTTCGTCAC[A/T]TTCTATCTCCTTTGA	146691
rs777476165	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17964412	TACAGAAATATGCTA[A/C]AAGTTGTTCTACAAT	146691
rs777488235	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17955772	GTTAGTTTTACAGTT[C/G]TTAAAGGCGGCGTGT	146691
rs777529542	snp	A/G	1.64727e-05	0.00286986	missense, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17884722	TCCTCATATATGTGC[A/G]CAACGCCGGTGAGAT	146691
rs777548802	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17888442	CCAATAAACCATTGC[C/T]GATTTAAACTATGGG	146691
rs777593836	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17877365	TCTGGGTTGTTTCCA[C/T]GGCCTAGCCAGCACT	146691
rs777622489	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17918915	GCTGATGAGGGCCCT[C/T]TATAAGTAAAATGAT	146691
rs777631998	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17896963	CCTCAGTGTAGGGAC[C/G]GCAGCCCTGCGCATT	146691
rs777669686	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17930709	TAATAATTTATACCC[A/C]AGACAAATAAAACAA	146691
rs777699955	snp	C/T	0.000674263	0.0183488	intron-variant	TOM1L2	GRCh38.p7	17:17869250	TCTCTCTCCCTCTCC[C/T]TCTCTTTCCTTTGTT	146691
rs777735503	snp	A/G	1.64773e-05	0.00287026	synonymous-codon, upstream-variant-2KB, intron-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17862769	GTTTCCTCTCGTCTG[A/G]GCAAACATGTCAAAG	146691
rs777765116	in-del	-/AG			intron-variant	TOM1L2	GRCh38.p7	17:17937329	TTTTTATCTTTGATC[-/AG]AGTCAACCAATAAGG	146691
rs777786312	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17881883	ACATTGCTTGACCCC[C/T]CTGCTTCAGTGAGGT	146691
rs777805155	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17911051	GCCAAAAAGCCAAGC[C/T]GCTGGATTGCGAGGC	146691
rs777805495	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17906520	GTCCTCATCTGACCA[C/G]GTTATATGTTTAATT	146691
rs777809730	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17892907	GCTTCCTGCCAACAG[C/T]CATGTGGGTGCACCA	146691
rs777875540	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17919941	GCCCCACAGTGTGCA[G/T]AGAGGAGGTAGCAAT	146691
rs777879455	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17951203	TGCAAGGAAAATGAC[C/T]AGCACCCAGTAGACG	146691
rs777880690	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17944239	CCGTGAGAGGCTGCC[G/T]GGTGAGTGGACAGGT	146691
rs777893465	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17939887	CTCATCTATAAAATG[C/G]AAGTGTTAAGAATTC	146691
rs777918519	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17932315	TTTTATTTTTTGTAG[A/C]GACAGAGTCTTGGTA	146691
rs777940466	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17856601	GGCCACAGCCTAGCA[C/T]AGCACACTATGGGCA	146691
rs777969705	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17899780	GTCTTTCCCAGCTTG[C/T]ACGTTTGTTAAGTCA	146691
rs777990022	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17966076	CAGTGAGCTGAGATC[A/G]CGCCACTGCACTCCA	146691
rs778006575	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17865297	CACAGACTTTTCTAA[A/G]CCCTGATGTGGCTTC	146691
rs778018173	snp	A/G	0.000112937	0.0075137	intron-variant, upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17972213	CGGTCCTCACCAGCC[A/G]GATCAGCGGCCGCCG	146691
rs778062547	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17958823	GTACATTTCAGTGTT[A/G]GAACTTTTAGCCGTA	146691
rs778083115	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17878351	CTCAGCTTCAAGAGC[A/G]GGCTGGTGTAGTTAC	146691
rs778106835	snp	C/G	2.09334e-05	0.00323516	intron-variant	TOM1L2	GRCh38.p7	17:17866265	AGTGGTAGGAAGTAG[C/G]TAGGCCCTTTTGTCC	146691
rs778120751	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17871187	CATCCTGGCTAATAC[A/G]GTGAAACCCCGTCTC	146691
rs778138312	snp	C/G			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17845039	TGTGCTCCCCAGATG[C/G]TGGGGTCTGGGAGCA	146691
rs778179861	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17884278	GACATCAAGCCCTGA[A/G]GTGCTATGGTGCTCT	146691
rs778194590	snp	A/C	1.72246e-05	0.00293462	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847646	CTGCTCACAGGGCGA[A/C]GAGGGCATCCTCTGA	146691
rs778207737	in-del	-/TAGC	0.000116989	0.00764729	intron-variant	TOM1L2	GRCh38.p7	17:17882910	CCTGGGCTGCCTGCA[-/TAGC]TGGACCTGGTACCTA	146691
rs778232045	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17954497	TTTGTATTTTTAGTA[A/G]AGACGGGGTTTCGCC	146691
rs778242923	in-del	-/A			intron-variant	TOM1L2	GRCh38.p7	17:17867509	CCAGTCAGGCAGTGC[-/A]GGGGGAGTTGGCTTT	146691
rs778283278	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17923053	AAAATTCCACACCAG[C/G]AGAAAGACTCCCAGA	146691
rs778304200	snp	A/G			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17844317	CAGCAGCTGCCCTGC[A/G]AGCATCTGTTGCCCT	146691
rs778365117	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17902096	CAGGAGAATTGCTTG[A/C]GCCTGGGAGGCGGTG	146691
rs778378450	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17914164	GTGGACAGAGGAGGG[A/G]TGTTCAGAGACAGCT	146691
rs778407290	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17872709	CTCTTTGCTCCAGCG[C/T]TCCAGGTGTCTGCGG	146691
rs778410649	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17877336	ACTGGGAGCAGCTTC[C/T]GTTGGTGGGAACATC	146691
rs778441930	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17935685	AGCTGAATTATACAC[C/T]TTATTATACCATCTC	146691
rs778516125	snp	A/G	1.65315e-05	0.00287498	synonymous-codon, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847725	CTCCATGGGGGGCGA[A/G]GGGAGGTCGGGAACC	146691
rs778535220	snp	A/G	3.3042e-05	0.00406447	intron-variant	TOM1L2	GRCh38.p7	17:17879763	TGGGGGCCACGAGGA[A/G]GGAAAGCAGGAAGGA	146691
rs778561601	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17886494	GCTGGCTGCCTCCAC[A/C]TGGTTCAAAATCCAG	146691
rs778610154	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17956140	TTACCACTACTGCCT[A/C]TGGCCCCACCCACAT	146691
rs778614085	snp	A/G	3.2981e-05	0.00406071	intron-variant	TOM1L2	GRCh38.p7	17:17884793	TAGAAGGCCTGTTAG[A/G]AAGCATTTCTCAGAG	146691
rs778616418	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17955859	GTTCGTAGTCTCGCT[C/G]GCTTCAAGAGTGAAG	146691
rs778637684	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17968115	GAGTAAGAATTACTC[C/T]ACCAACCGCTCAGAC	146691
rs778659575	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17933982	GGTGACTCACTGCCT[A/G]GAAAGGCTTGCCCCT	146691
rs778667027	snp	A/G	3.31554e-05	0.00407144	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17869347	GCTCCCACCTCTCGT[A/G]TCGAAGGAAGACGTT	146691
rs778678639	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17851443	GGCAGCACCAGCCCC[A/G]GGGGGATGCAGGGGG	146691
rs778682093	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17896933	TGAGACCATGCAAAG[C/T]GCGCTAGGATGGGGC	146691
rs778686466	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17866595	GTGGGCCTGGATGTC[A/G]GTGAGCCCTGCTCAC	146691
rs778688465	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17901269	GATTAGATAGTGTGG[A/G]GTTGGAAACCAGGAG	146691
rs778713581	in-del	-/TTTTTTT					GRCh38.p7	17:17952377	TGCTTCTTTATTTTC[-/TTTTTTT]TTTTTTTTTTTTTTT	146691
rs778757730	snp	C/T	1.65649e-05	0.00287788			GRCh38.p7	17:17893718	GTTGTTCTTGGGAGA[C/T]ATAATTTTGACCAGA	146691
rs778758776	snp	A/G	3.29625e-05	0.00405958			GRCh38.p7	17:17850899	GAGTCTCACCAGGTC[A/G]GTCCTGAGCCACACC	146691
rs778776857	in-del	-/G	1.65564e-05	0.00287714	frameshift-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847715	GGCAGGAGCCTCCAT[-/G]GGGGGGCGAGGGGAG	146691
rs778799644	snp	A/C			intron-variant, nc-transcript-variant	TOM1L2, LOC100507131	GRCh38.p7	17:17859162	GCTCACTGCAACGTC[A/C]GCCTTTGGGTTCAAG	146691
rs778802696	snp	A/C			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17846930	TGCCTGCTGCCCTCC[A/C]AATTGTCCTTGGCCC	146691
rs778807083	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17942555	CCGATATGTATGGGC[C/T]GATATGTACACCTTC	146691
rs778825659	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17884832	GTATCTGAAAATCCA[A/G]AGTGGCCCACGTCCT	146691
rs778829767	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17896689	GGTAATTTTCCAGAA[C/T]GAAGCCAAAAGCCAT	146691
rs778840424	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17852287	AGTGATGTGACAACT[C/T]CAGTCCTGGGGGTTG	146691
rs778866096	in-del	-/AT			intron-variant	TOM1L2	GRCh38.p7	17:17906132	TTGTCTTCTCTTTTC[-/AT]TTTTTTTTTTTTTGA	146691
rs778872607	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17909156	ACTGCATTCCAACCC[A/G]GGCGACAGAGCCAGA	146691
rs778943790	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17955551	TCACCATATTGGCCA[C/G]GACAGTCTTGATCTC	146691
rs778958684	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17895477	ACTATATGCCAGGCA[C/G]TATGAGAGATCCTTC	146691
rs778991720	snp	A/G	1.6492e-05	0.00287154	intron-variant	TOM1L2	GRCh38.p7	17:17850963	GGGATCTATGGAGGC[A/G]GCAAGCAGCGGGCCA	146691
rs779014895	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17935882	CAAATTCTGAGGAAT[G/T]ACTCACACTGGTGGT	146691
rs779019783	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17904384	GCAATTCACTGGAAA[A/G]TAAGAGTTGCCAACA	146691
rs779054214	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17869990	TCCATAGGACAGGTT[C/T]CTTAGCAGGGAAATT	146691
rs779059206	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17918688	ACCTTCTTTGCTGCC[A/G]CCCACAAGAGAGGCC	146691
rs779061452	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17908059	ATTATTAAAAATCAA[C/T]TGCAGTAGTTAAAAA	146691
rs779110751	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17930447	CCCTCACGGTAGACA[C/G]ACACCTGGCAGGCCC	146691
rs779113149	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17893987	CCCACACTCCATTCT[A/C]CAGGGATGACAGCAG	146691
rs779124310	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17950994	TGTTTCATCTTCCCC[A/G]CTAGGGGGAAGATCC	146691
rs779157435	snp	C/T	1.64792e-05	0.00287042	synonymous-codon, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17882810	ACCAGCACTTGTCCT[C/T]TGCTGTGATTGGGAC	146691
rs779175243	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17949820	GCCAGGGCAATGTTA[C/T]AACACTGAATCTGTT	146691
rs779175296	snp	A/G	0.000107152	0.00731879	missense, upstream-variant-2KB, nc-transcript-variant	TOM1L2, DRC3	GRCh38.p7	17:17972265	ACGCGGCCTTACCGA[A/G]GCACTGCCCCACTGG	146691
rs779193017	snp	A/G			upstream-variant-2KB, intron-variant	TOM1L2, DRC3	GRCh38.p7	17:17973339	ACTGACCTCATAACT[A/G]TCAAATGATTTCATC	146691
rs779194814	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17956895	GGCGGCTCCGGCCTC[A/G]GCCAGCCCAGGGAGG	146691
rs779220243	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17882578	CCCCTGGGGATTGAG[C/G]CCTTCCATCTCTGTG	146691
rs779225751	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17892609	TCCCATCTCCTGCCT[A/G]CTCCCCCACCCCAAG	146691
rs779234293	snp	C/T	1.6513e-05	0.00287336	intron-variant	TOM1L2	GRCh38.p7	17:17847796	ACTCTGCAATACAAA[C/T]CAAGGCAAGGGTCAG	146691
rs779246477	snp	C/G	1.72042e-05	0.00293288	intron-variant	TOM1L2	GRCh38.p7	17:17893847	AAGGGTCACCCCAGT[C/G]GGAGCTGGAGAAGAC	146691
rs779274554	snp	C/T			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17844085	CTCCCAGGGACCACT[C/T]CAGCAGTGCCAGAGG	146691
rs779319299	snp	A/G			utr-variant-5-prime, upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17972452	AGGGCCTTTGGCCCC[A/G]CCCCCTTGCCGCGTC	146691
rs779346878	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17881729	GAGCAGCAGAGCTGG[G/T]GGCTCACACCCAGGC	146691
rs779386287	snp	A/G	5.9657e-05	0.00546122	synonymous-codon, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17866402	TATTAAGTTGTCTTC[A/G]GTTACTTCATTCAGT	146691
rs779424686	in-del	-/C			intron-variant	TOM1L2	GRCh38.p7	17:17894369	GTTTGTGGACCTCAG[-/C]TGCCAGGTGACTTTA	146691
rs779426666	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17933715	GATATTTACTCTCAT[C/T]CTCTTTCCTTCCCCT	146691
rs779444255	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17876984	GGAGGATTTGACGCA[C/T]AGCTCAAGAGGAGGA	146691
rs779468648	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17939651	TTTGTAGAAGTTCAT[C/T]ATACTATTCTACTTT	146691
rs779517398	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17901045	AGGGCTCTCCTGGTG[C/T]GGGGGCCACGGGGTG	146691
rs779521366	snp	C/T	1.64773e-05	0.00287026	missense, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17884756	GACTGCTTCGAAAGG[C/T]ATCAGCCCATGCCTG	146691
rs779530451	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17854587	TGGTGTGCAGTGGTG[C/T]GATCTCAGCTCACTG	146691
rs779535298	snp	C/T	1.65685e-05	0.00287819	intron-variant, missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17893741	TGACCAGAACACTGT[C/T]GATGAAATCTCGGTT	146691
rs779536575	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17890466	AAGTCAAGTGCTAGA[C/T]GCTCATAGCAGCATT	146691
rs779537615	in-del	-/AG			intron-variant	TOM1L2	GRCh38.p7	17:17919084	AGGGAGTGTGAACTC[-/AG]ATTTTGGTGAGTTCT	146691
rs779559828	in-del	-/TC			intron-variant	TOM1L2	GRCh38.p7	17:17903163	GCTATATATAGCTTC[-/TC]TCTCTCTCCCTGCCC	146691
rs779566865	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17923066	AGGAGAAAGACTCCC[A/G]GAAGTTTCCCAGGGC	146691
rs779613781	in-del	-/AG			intron-variant	TOM1L2	GRCh38.p7	17:17911952	CACAGCACATGTTTC[-/AG]AGAGCACAGGGTTGG	146691
rs779631050	snp	A/G	1.65754e-05	0.00287879	synonymous-codon, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847701	AGGGTTTGAGGCTGG[A/G]GCAGGAGCCTCCATG	146691
rs779636802	snp	A/G	4.95987e-05	0.00497965	intron-variant	TOM1L2	GRCh38.p7	17:17862879	AAATGGGTGGCAGAT[A/G]AGAACAAAATGTAGA	146691
rs779643729	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17899694	GGGGAGCCCTCAGTC[C/T]GGCTGTGGGCCAGCG	146691
rs779661750	in-del	-/T			intron-variant	TOM1L2	GRCh38.p7	17:17876204	GGTAAGGGCATGCAC[-/T]TTAGCAGGGACAGAT	146691
rs779716266	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17958354	ACCAGTGCCAGAAAA[A/T]GTAGATAAAACAGAA	146691
rs779733605	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17849135	AGAAAACTCCAAAAA[C/T]GGTGCAGGCTGGTTC	146691
rs779766547	snp	C/T	1.6519e-05	0.00287388	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17869416	CCTCCTCATTGGACA[C/T]GCGGGAGATGAGCTC	146691
rs779784962	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17855900	GTACTCAGGAGGCTT[C/G]AAAAGACTCAAGGTT	146691
rs779788493	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17945424	AGTAGCTGTTCTCTG[A/C]GAGAACACTTATACA	146691
rs779798611	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17878048	CAGCAGGAATTCCGA[C/T]GCTGACACAGCACAA	146691
rs779828956	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17864932	TACAGCAACTGATAG[A/C]CACTAGAAGTTTAAC	146691
rs779872854	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17885001	AAAACACAAAACTTA[A/G]TTTAGCATGTATTTC	146691
rs779887079	in-del	-/AC			intron-variant	TOM1L2	GRCh38.p7	17:17957738	CATATCACAGGCTAT[-/AC]ACACACACACACGTA	146691
rs779892956	in-del	-/TTT			intron-variant	TOM1L2	GRCh38.p7	17:17932912	TGGGGATTTAAATTA[-/TTT]TTCATTTTTAATTGC	146691
rs779893258	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17871392	AAGTATTCAGAGGCC[A/C]AGTGCGGTGCCTCAT	146691
rs779897100	snp	A/C	8.35499e-05	0.00646281	intron-variant	TOM1L2	GRCh38.p7	17:17869490	TAGGGAACACATGCA[A/C]CTCTGGGTAGCCTGC	146691
rs779900262	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17868472	GTGAGTCAGCTGGTG[C/T]GGCAGAGGGGACCAG	146691
rs779910323	snp	A/G	1.66101e-05	0.0028818	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17861453	AGAAGACTCCAGGCA[A/G]AAAAACAGGGTTAAA	146691
rs779918700	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17863066	CTCAAACTGCTCAAG[A/G]AGGCGAAAGAGTCAT	146691
rs779939927	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17954212	ACAGAAAAGGAGGGA[A/G]TGGGAACGGCAAAGT	146691
rs779948108	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17961494	GCAGGAGGATTGCTC[A/G]AGTTCAGAAGTTCGA	146691
rs779971888	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17908252	AATTGGATTGCCACA[G/T]GCAAAAGAATGAACT	146691
rs780038631	in-del	-/AGGTCT			intron-variant	TOM1L2	GRCh38.p7	17:17952585	TTCTTTGTAGCAACA[-/AGGTCT]TACTGTGTTGCCTAG	146691
rs780064550	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17968039	CTTGAGATGAACACG[C/T]TAAGTGTTCTACTAA	146691
rs780099057	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17907050	TCCCTCCATGGACAC[A/G]GTGGTGCTCTCTGAC	146691
rs780116406	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17867185	TGGAGGTCATTGTGA[G/T]TGTCCCCAGCCTCTC	146691
rs780179718	snp	C/T			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847094	ACCCAGCAGAGCCTT[C/T]TCAAATGCTGATAAG	146691
rs780252990	snp	C/T	1.64928e-05	0.00287161	synonymous-codon, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17848842	ACTTGTGACACCCTC[C/T]TCCAGATCATCACCC	146691
rs780253891	in-del	-/CT			intron-variant	TOM1L2	GRCh38.p7	17:17966679	AGATTCTAGGCTTCA[-/CT]CTGCCATTGACCTTG	146691
rs780259520	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17896547	GCCACAGAGCAGCCC[C/T]AAAGCCTATCTGAGC	146691
rs780262199	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17928624	AATTGCACTCTTCTG[A/G]GATCTCACAGTCCTC	146691
rs780267534	snp	A/G			intron-variant, upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17971204	GAGGAAGCAACAGTC[A/G]ATGTGCAGAGTACTA	146691
rs780273765	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17924031	TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG	146691
rs780322281	snp	C/T	3.29603e-05	0.00405944	synonymous-codon, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17882825	CTGCTGTGATTGGGA[C/T]CTGGGCATGGTCGCA	146691
rs780334675	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17937201	GGCAGGCTATTCAAC[A/G]TGAACCCTTCCTCCC	146691
rs780360775	snp	C/G	3.29484e-05	0.00405871	synonymous-codon, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17866885	ACTTACTCCATTACT[C/G]GCATTTTGAACGGAT	146691
rs780385874	snp	A/G	1.64925e-05	0.00287158	synonymous-codon, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17879680	GGACCATTTCTGTTA[A/G]CATCTCAGACATGAC	146691
rs780398631	snp	A/G			intron-variant, upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17971011	AAGTCCCATATGGTG[A/G]CCATTTCAGTATTCC	146691
rs780481486	snp	C/T			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17845355	ACCAGCTGGCGCTGG[C/T]GCTGGAGCTGGAGCG	146691
rs780483960	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17918617	ACTTCTGTCTGGAAA[C/G]CCTTCTCTCCAGCCT	146691
rs780498700	snp	G/T			intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17862116	CAAGCAGGACTCAGG[G/T]TGCTGAGTGCACCAA	146691
rs780501308	snp	C/G	3.35728e-05	0.00409698	intron-variant	TOM1L2	GRCh38.p7	17:17907416	CCCTAAAAGCTCAGA[C/G]AGGCTTCCCAGGAGA	146691
rs780511852	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17853264	CCACACTAGCGGTTA[C/G]AGTGTGCACCAGCCC	146691
rs780585626	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17890268	TCTTGGGTGCTGGTG[A/G]CTGAGAACACCCAAG	146691
rs780601686	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17868242	TCCTGGGGATGCCCC[C/G]ACACTTACTGCAGAG	146691
rs780608703	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17956795	AGCTCACGCCCACCC[A/G]GAACTCGCGCTGGCC	146691
rs780654742	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17898487	GCCCAGGCACCAAGC[C/T]ATTCAGAGGTTGTGC	146691
rs780668460	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17902690	CAGTGAATCCACCAA[G/T]ATAGTCACCAAGACT	146691
rs780707839	snp	C/T	1.65564e-05	0.00287714	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17847713	TGGGGCAGGAGCCTC[C/T]ATGGGGGGCGAGGGG	146691
rs780714535	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17894370	TTTGTGGACCTCAGC[G/T]GCCAGGTGACTTTAA	146691
rs780748143	in-del	-/G			intron-variant	TOM1L2	GRCh38.p7	17:17856952	TACTCTGTTTCTACT[-/G]TGTTTATTTTTTTAT	146691
rs780775292	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17922171	CAGGACACAGGGCAC[A/C]GACCTGAGGCTGAAC	146691
rs780781643	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17910600	TGTGAGACAGAGTCT[C/T]ACTCCATTGTGCAGG	146691
rs780792080	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17961764	GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG	146691
rs780828291	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17919606	TAGTAAAAAGATTCC[C/G]CATAAGTCCACATTT	146691
rs780833117	snp	A/G	1.69539e-05	0.00291147	intron-variant	TOM1L2	GRCh38.p7	17:17893825	CCTGATGTGGGGAGG[A/G]AAGGAAAAGGGTCAC	146691
rs780839066	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17944999	GCCCGCACTGCCGCC[A/G]CCACACTAATCCTTC	146691
rs780870495	snp	A/G	1.65745e-05	0.00287871	intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17861462	CAGGCAGAAAAACAG[A/G]GTTAAAGACCTACCC	146691
rs780906114	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17952781	GCTTTAGGATGCCCA[C/G]TATGCACAAAAGACC	146691
rs780918008	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17956351	AGCTAGACACAGAGT[C/G]CTGATTGGTGTATTT	146691
rs780920994	snp	C/G	3.35909e-05	0.00409809	intron-variant	TOM1L2	GRCh38.p7	17:17869500	ATGCACCTCTGGGTA[C/G]CCTGCTGGGTGTGCT	146691
rs781027451	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17875552	TTCCTAAACGCTGAC[A/G]ACTTCAGCTTTGGCC	146691
rs781046166	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17849023	GTAATAGTAAAATAC[C/T]GCTCTTCTTATTGGA	146691
rs781100672	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17921628	GCCAGCTTGTCCCAG[C/G]CTAGCAGGCTGTGCT	146691
rs781125700	snp	A/G	6.39366e-05	0.00565369	intron-variant	TOM1L2	GRCh38.p7	17:17869216	ATTAGCATCTCTGAT[A/G]AGTATTTTCCAACTC	146691
rs781130664	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17920008	CTGGCCTTGGACCCT[C/G]ATCCATCCTCAGGTA	146691
rs781144572	snp	C/T			intron-variant, upstream-variant-2KB	TOM1L2, LOC100507131	GRCh38.p7	17:17861230	CAGCCTGTCTCCCAC[C/T]TGCCTGGGACTGTTT	146691
rs781156044	snp	A/G	1.64868e-05	0.00287109	missense, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17879647	GCAACTCCAGATCAG[A/G]TGAATCCTCCTGTCC	146691
rs781173638	snp	A/C	6.58913e-05	0.00573945	synonymous-codon, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17884691	CATGGGAAATTCAAC[A/C]CCTTTCCTCTTCAGC	146691
rs781229912	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17933425	TCCAAACAAAATCAG[A/G]CTCCGTCAGAAAAGA	146691
rs781262054	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17959102	GTCACGAAAATGTAA[A/G]TAAAGTGTTGTCCTG	146691
rs781270422	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17878639	GACCAAGACTGACAA[C/T]GGAGGGCCAGACACA	146691
rs781283244	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17931894	GTCTCCAAATACCCA[A/T]GCAAATCACATTAAT	146691
rs781323089	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17906890	GAAGAAGTACAAATA[C/G]AGTGCAGCTGTAAAA	146691
rs781331390	snp	C/G/T			intron-variant	TOM1L2	GRCh38.p7	17:17872299	CGTGAAGGATTCCAA[C/G/T]AGCCAGGACTGAAGT	146691
rs781385369	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17941099	GGAGACCATTTCTCC[A/G]GTGAACAGGTGGAAG	146691
rs781398608	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17945316	CTCTCTCTCTCATTC[C/T]TTGATGAATTATTTA	146691
rs781401020	snp	C/G	1.78784e-05	0.00298979	intron-variant	TOM1L2	GRCh38.p7	17:17907579	TCTCCTGGAATAAGT[C/G]GGCCTTGGCAGGAAA	146691
rs781427105	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17955271	GGCAGAGGGCCCTCA[C/T]TTCTCAAACCACAGC	146691
rs781445737	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17851700	AGCCCTGAAAGCAAC[A/C]GCTCCCTTTAGTCTC	146691
rs781445986	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17948347	TGGAGCTTCTGTGCA[A/G]TCAAAAAATGTGCCC	146691
rs781450532	snp	C/T			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17845110	CCCACTCTGGGGCAC[C/T]GGGGCTATACTTGCT	146691
rs781526846	snp	G/T	3.31192e-05	0.00406921	intron-variant	TOM1L2	GRCh38.p7	17:17879790	AGGAAAGGTCAGTCA[G/T]CCTGCACTTGCAATA	146691
rs781535968	snp	C/T			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17844382	GCTGGGTCCTCTCCT[C/T]CCCAGGGGCTGGAGT	146691
rs781540091	snp	A/G			intron-variant, missense, downstream-variant-500B	TOM1L2, LOC100507131	GRCh38.p7	17:17857852	GGGCCGAGGACAGAA[A/G]AGTCTCAGAAAGAAA	146691
rs781565426	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17853133	AGGACACACCAGTTA[C/T]CATGCTCTCAATGAC	146691
rs781572421	snp	A/T			intron-variant	TOM1L2	GRCh38.p7	17:17960997	GAGTATAAAAAGGCA[A/T]CCCACAGAATGGGAG	146691
rs781580283	snp	A/G/T	4.98271e-05	0.00499114	intron-variant	TOM1L2	GRCh38.p7	17:17907437	TCCCAGGAGAGGGGG[A/G/T]CACACGTACCCTTCC	146691
rs781590984	in-del	-/TCTC			intron-variant	TOM1L2	GRCh38.p7	17:17969860	GTGAATAGGAATCTT[-/TCTC]TCTCTCTCTCTCTCT	146691
rs781604349	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17949186	TCTTGCCACCTGCCA[C/T]TAAGGGTCTCCACCT	146691
rs781610588	snp	A/G	1.6483e-05	0.00287076	synonymous-codon, intron-variant, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17882729	ATTGGCTGTGATGGG[A/G]CCAGTCACACTCAGA	146691
rs781624109	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17856844	CAGACAAGGCAGGAG[A/G]GACCCTTGCAGGTCT	146691
rs781650728	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17943556	AGTGCAAATGCATGG[A/G]AAGGGGAGCCCGAAG	146691
rs781670311	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17902301	GCTGATGGTGACCTC[A/G]GCTCTGGACATTAGG	146691
rs781729635	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17900475	TGCAGTGAGCTGAGA[C/T]TATGCCACTGCACTC	146691
rs781734789	snp	A/T			intron-variant, upstream-variant-2KB	TOM1L2, DRC3	GRCh38.p7	17:17971695	CTGGATAAAGACACA[A/T]GCAGTGGCATCTCCC	146691
rs781748969	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17901357	AATCAGTGGCCTGTG[C/T]TGAGATGGCATCAAG	146691
rs781749023	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17917196	AATTAGCTGGGCGTG[G/T]TGGCGCACACCTGTT	146691
rs781757565	snp	A/C			intron-variant	TOM1L2	GRCh38.p7	17:17865423	GAGTCGTCCCCCAGG[A/C]TGGAGTGCAATGGCG	146691
rs796109976	in-del	-/TC			intron-variant	TOM1L2	GRCh38.p7	17:17969880	CTCTCTCTCTCTCTC[-/TC]AGAAGACTGACAAAC	146691
rs796129390	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17890422	CTTAATATATTCCCA[C/T]TAAAAAGGAATATAT	146691
rs796145399	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17967638	TGGAGATGCAGTCTC[A/G]CTCTGTCATTCAGGC	146691
rs796179760	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17964968	GGCAATTAAGGACAA[A/G]TGCTCTAGACTAGAC	146691
rs796284800	in-del	-/GGGAGA			intron-variant	TOM1L2	GRCh38.p7	17:17913258	AGACCGTGGGGAGAC[-/GGGAGA]GGGAGAGGGAGAGGG	146691
rs796298183	multinucleotide-polymorphism	CT/GG			utr-variant-3-prime, nc-transcript-variant	TOM1L2	GRCh38.p7	17:17846911	TGGCCACCATCTGCG[CT/GG]CTGCCTGCTGCCCTC	146691
rs796315171	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17931242	TAAATCCTTCCTCTT[C/T]TACAGATTTCCCCAA	146691
rs796319237	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17904833	GGACACATTTCTCCT[C/G]CCATCCTGGAAGACA	146691
rs796329951	in-del	-/AA			intron-variant	TOM1L2	GRCh38.p7	17:17869309	CAATCTTTTCAAGGG[-/AA]AAAAAAAAAAAAAGA	146691
rs796369675	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17887648	ACCTGGCTAATTTTT[G/T]TATTTTTTGTAGAAA	146691
rs796386838	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17963884	TGCAGGACACCGTGC[C/T]AGGGATTTTAAGCAC	146691
rs796392233	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17944598	AGATTCCCATATTTG[A/G]AGTTATTCTCCCCAA	146691
rs796441654	in-del	-/A			intron-variant	TOM1L2	GRCh38.p7	17:17877877	CTGATGGGCTTGTTT[-/A]AAAAAAAAAAAAAAA	146691
rs796468771	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17961670	TGAGGTGAGGAGATC[A/G]AGACCATCCTGGCTA	146691
rs796470396	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17911452	ACTTGCCCCACTGTT[C/G]CCTAGAACACTTGTG	146691
rs796476150	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17926773	TGAGGCACAAGAATC[A/G]CTTGAACCTGGGAGG	146691
rs796502316	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17909876	TCTACAAAAAATTTA[A/G]AAATTAGCTGGGCAT	146691
rs796538907	in-del	-/GA			intron-variant	TOM1L2	GRCh38.p7	17:17869308	ACAATCTTTTCAAGG[-/GA]AAAAAAAAAAAAAAG	146691
rs796618240	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17955351	TTTTTTTTTTTTTTT[G/T]TTTTTGAGACAAGAG	146691
rs796659224	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17879169	TACAAGGGCTCCTGT[A/G]CACAGTCAAGGTTGA	146691
rs796709401	snp	G/T			intron-variant	TOM1L2	GRCh38.p7	17:17966745	CTTATGTGATACAGG[G/T]ATGATAACACCCAAA	146691
rs796712685	in-del	-/C			intron-variant	TOM1L2	GRCh38.p7	17:17878511	CACCCCCATAAGAGC[-/C]GATGGCTTTGGAGTA	146691
rs796715140	snp	C/T			intron-variant	TOM1L2	GRCh38.p7	17:17956861	CCTCTCCCTCCACAT[C/T]TCCCTGCAAGCTGAG	146691
rs796724347	in-del	-/AA			intron-variant	TOM1L2	GRCh38.p7	17:17885948	AAAAAAAAAAAAAAA[-/AA]TTCTGTTCTTTGGAA	146691
rs796746629	in-del	AGAT/CAAGCTCTACCTCCTGGGTTCACG			intron-variant	TOM1L2	GRCh38.p7	17:17916152	ATCTCAGCTCACTGC[AGAT/CAAGCTCTACCTCCTGGGTTCACG]CCTTCTCCTGCCTCA	146691
rs796803455	in-del	-/TCTC			intron-variant	TOM1L2	GRCh38.p7	17:17945602	CATACATACCCATCT[-/TCTC]TCTATTTACAGCCTA	146691
rs796876803	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17891182	TGGCCAGCACACACT[A/G]CTACTGCCAGACCAG	146691
rs796888144	in-del	-/G			intron-variant	TOM1L2	GRCh38.p7	17:17917382	GTTGTTTGGCTATTT[-/G]GGGTCCCTTGAGATT	146691
rs796898959	in-del	-/A			intron-variant	TOM1L2	GRCh38.p7	17:17925855	GTGAGACCCTGTCTC[-/A]AAAAAAAAAAAAAAA	146691
rs796904384	snp	C/G			intron-variant	TOM1L2	GRCh38.p7	17:17949767	AGAGCACTCCTCAGA[C/G]AGTGGCCTGCAGATC	146691
rs796914464	snp	A/G			intron-variant	TOM1L2	GRCh38.p7	17:17913958	CAGCTTGAGTTCTGT[A/G]AAGGGGAGAGACTAC	146691
rs796964580	in-del	-/A			intron-variant	TOM1L2	GRCh38.p7	17:17875269	CAAAAAGAAAAAAAG[-/A]AAAAAAAAAAAAAAA	146691

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