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

TOM1

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs368880702	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35341761	CCCACAGGGAGGAAA[C/T]GCACCACACAACTCC	10043
rs368935761	snp	C/T			intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35333998	CCCCATTTTGCATCA[C/T]TAATGCTATACTTTT	10043
rs368995430	snp	C/G			intron-variant	TOM1	GRCh38.p7	22:35317076	TGCCTCTAGGAAGAG[C/G]GGGCTGGGGCAGGGG	10043
rs368997639	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35318046	TTCCAGGGAGCCCCT[A/G]CCCCAGCCCCATTGC	10043
rs369055636	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35302238	CTTGTTAAATAATGT[C/T]GGGGCCCCAACCCCA	10043
rs369065347	snp	A/G	0.00478085	0.0486577	intron-variant	TOM1	GRCh38.p7	22:35302484	CGGGATTACAGGCAC[A/G]CTCCGCCACACCCGA	10043
rs369085232	snp	C/T	0.000701051	0.0187092	intron-variant	TOM1	GRCh38.p7	22:35346981	GAAGGTAGTAGTCCC[C/T]GCCCCTGCCCGCCCT	10043
rs369112238	snp	C/G			intron-variant, downstream-variant-500B	TOM1, MIR3909	GRCh38.p7	22:35335896	CCATTTCAGGCACTA[C/G]GAACAGCATGTGCAA	10043
rs369114634	snp	G/T	0.000150702	0.00867919	intron-variant	TOM1	GRCh38.p7	22:35323189	CCAGGTGAGTGCCAG[G/T]ACAGGGCAGGGCACG	10043
rs369150706	snp	A/G			intron-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35337378	AGCAGGCCTTCTCTG[A/G]GTCAGAAGTCAGCAA	10043
rs369281525	snp	C/G	0.000153988	0.00877328	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35347139	CTGAGGGGCCCCCGG[C/G]TCCCCCATCTGGCCC	10043
rs369332706	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35328261	CCAGTAAGGGCTCCG[A/G]AAGAGAGAAGACTGC	10043
rs369343111	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35317001	TGTTAGTAATGGAGC[A/G]TTTGCTTCCTAGGTA	10043
rs369344190	snp	A/G	4.94686e-05	0.00497311	intron-variant	TOM1	GRCh38.p7	22:35345794	GACGTGGTATGTTGG[A/G]GCCCACTCCTCACCC	10043
rs369385770	snp	A/C			intron-variant	TOM1	GRCh38.p7	22:35303131	TCCACCTCCCCTCCC[A/C]ACACACACACACACA	10043
rs369412767	snp	C/T			intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334550	GGAAGGGCACACGGA[C/T]CCTGCTTAGTAAGCA	10043
rs369485648	snp	A/G	1.6679e-05	0.00288777	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35347081	TTCCTGGAAGAACGG[A/G]CCAAAGCCGCGGACC	10043
rs369494560	in-del	-/CA			intron-variant	TOM1	GRCh38.p7	22:35300906	CCATATAAAAAAAAA[-/CA]GTTGTAATATTTATT	10043
rs369506084	in-del	-/A			intron-variant	TOM1	GRCh38.p7	22:35310551	GTGAGACTCTGTCTC[-/A]AAAAAAAAAATGTAT	10043
rs369651820	snp	G/T	0.000115486	0.007598	intron-variant	TOM1	GRCh38.p7	22:35345821	ACCCACACAGCAGGA[G/T]GACCCGTTGTTCTCA	10043
rs369662655	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35302224	AATTCCTAGGAGGGC[C/T]TGTTAAATAATGTCG	10043
rs369683318	snp	A/G	1.64743e-05	0.00287	utr-variant-5-prime, missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35317904	ATGGCTCCCTGCAGA[A/G]CGAGGACTGGGCCCT	10043
rs369720490	snp	C/G	1.68783e-05	0.00290498	intron-variant	TOM1	GRCh38.p7	22:35323213	GGGCACGGCCAGGAA[C/G]AGCTGTCAGTGCAGG	10043
rs369730160	snp	C/G			intron-variant	TOM1	GRCh38.p7	22:35300318	CGTGGTTGGCAGTGG[C/G]TGGGCCACTCTGCTG	10043
rs369817715	in-del	-/ACCTACACACTCATACACCTACACACCCCCACAC			intron-variant	TOM1	GRCh38.p7	22:35342885	CACCCCTACACACAC[lengthTooLong]CACACACACATCTAC	10043
rs369952232	snp	A/G	0.000380087	0.0137804	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35330411	TCCCTCAGATCGCCA[A/G]TGAGCAGCTGACAGA	10043
rs369956519	snp	A/T			intron-variant	TOM1	GRCh38.p7	22:35303669	TGCCCGGCTAATTTT[A/T]GTATTTTTAGTAGAG	10043
rs369971492	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35322844	TAGGCCGTGCCCTCC[A/G]GTAAACAAGTCCCCC	10043
rs370123651	snp	A/T	0.00119737	0.0244387	intron-variant	TOM1	GRCh38.p7	22:35329257	CACCGGGTGTAGCCA[A/T]TTTTTTTATTTTTCA	10043
rs370196286	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1	GRCh38.p7	22:35324938	ACCCACCTCAGAGCA[A/G]GTGGCACCCTGGGCA	10043
rs370245441	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35325842	CTTTTGTCTCTTGGG[A/C]CATGTTAAGACATCA	10043
rs370264729	snp	A/G			intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35335613	CTGGAGAACCCTGGC[A/G]CCTGCCCTGGTCACC	10043
rs370310071	snp	A/G	0.000132048	0.00812444	intron-variant	TOM1	GRCh38.p7	22:35345789	CCACTGACGTGGTAT[A/G]TTGGGGCCCACTCCT	10043
rs370310445	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35333719	GATCTCAGAAATCCT[A/G]CCATCCTAGGATTGG	10043
rs370359842	snp	A/C			intron-variant	TOM1	GRCh38.p7	22:35310028	CACATGGTAGGGTTA[A/C]TAAAAATTTCACATA	10043
rs370418030	snp	A/G	0.000149809	0.00865344	synonymous-codon, nc-transcript-variant	TOM1	GRCh38.p7	22:35347092	ACGGGCCAAAGCCGC[A/G]GACCGATTGCCCAAC	10043
rs370472618	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35339072	GTGGTGGCTCACACC[C/T]GTAATCCCAGCACTT	10043
rs370515099	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35319626	CCCCAGGTCAGTGGC[A/G]CATGGCGGAACATGC	10043
rs370544258	snp	A/G	3.29576e-05	0.00405928	missense, intron-variant, nc-transcript-variant	TOM1	GRCh38.p7	22:35323601	ATGACTGACCTGGAC[A/G]TGCTGTCACCCATCC	10043
rs370649560	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35330038	TAATCCCAGCACTTT[A/G]GGAGGCCGAGGCAGG	10043
rs370726976	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35329974	CAGGGGCTGGAGGCC[C/T]GTGCATTAGAGATGG	10043
rs370787206	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35324688	TGAGTAGCTGGGACT[A/G]CAGGCATGAGCCACC	10043
rs370798451	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35318497	TGGTGTTGGGGTCAC[A/G]GTATCGTCTTGCTCA	10043
rs370914527	snp	A/G			intron-variant, upstream-variant-2KB	TOM1	GRCh38.p7	22:35299485	CAGCCCAGAGAGGCT[A/G]TCACCCAGGGTAGGT	10043
rs370926538	snp	C/G	4.94173e-05	0.00497053	intron-variant	TOM1	GRCh38.p7	22:35333031	TAAAAGTCTTCTTTT[C/G]TGTGACTAGATCAGG	10043
rs370952296	snp	G/T	3.37952e-05	0.00411053	intron-variant	TOM1	GRCh38.p7	22:35333363	GAAAGGAACGAAGCT[G/T]CAGACAGCGGGGATG	10043
rs370955972	snp	G/T			intron-variant	TOM1	GRCh38.p7	22:35314966	TAATGCTGCTTGATA[G/T]TCTATGGCATATAAC	10043
rs370968300	snp	C/T	1.65277e-05	0.00287464	intron-variant	TOM1	GRCh38.p7	22:35318008	GAGACGGCCATCCCA[C/T]CACGCAGCACACTCC	10043
rs370999345	snp	C/T	0.000132866	0.00814956	intron-variant	TOM1	GRCh38.p7	22:35322074	CCTGTGGCAGGACTA[C/T]GGTCCACTGAAAGTC	10043
rs371002429	snp	C/G/T	0.000117976	0.00767954	intron-variant	TOM1	GRCh38.p7	22:35346880	CTGCCCCAGGCTGAC[C/G/T]GTACTGGGGGCCCGG	10043
rs371008974	snp	C/G			intron-variant	TOM1	GRCh38.p7	22:35342933	CCACACGTCATACCT[C/G]CACTCATACACCTAC	10043
rs371013420	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35343537	CACACCACACACACA[C/T]CTACACCCACCACAC	10043
rs371074047	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35302898	AGGAAGTACTGCTCC[C/T]TGGCTGTGATTACTG	10043
rs371088274	snp	A/C/G	0.000135883	0.00824156	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35323771	TCCTCCCACTAGACC[A/C/G]TGTTCAACTCAGAGA	10043
rs371177891	snp	C/T	8.46633e-05	0.00650572	intron-variant	TOM1	GRCh38.p7	22:35338822	CTGCCACCCTGGGGC[C/T]CTCCTGAAGGAGGTG	10043
rs371178160	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35338627	TGGAGGATGGGAGCC[A/G]TCAATCTGTGCCCCC	10043
rs371189937	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35305358	AGGGTTGATGCCAGA[A/G]GGAAGAAAGAAACTG	10043
rs371317428	snp	G/T	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35315022	TGGAAGGGCATGCAG[G/T]CCAGGTCGAAGACTA	10043
rs371323267	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35346282	GAGCAGAAGGGGCAG[A/G]GCCAGACTCAGCTTC	10043
rs371363414	snp	C/T	0.000153988	0.00877328	intron-variant	TOM1	GRCh38.p7	22:35346923	TCCTTTCCTTCTACC[C/T]TCCCAGGGTAATGAT	10043
rs371431626	in-del	-/AAAG			intron-variant	TOM1	GRCh38.p7	22:35313362	AAAAAAAAAAGAAAG[-/AAAG]GGGTGATACCATACC	10043
rs371441856	snp	A/G	7.1623e-05	0.00598384	synonymous-codon, nc-transcript-variant	TOM1	GRCh38.p7	22:35323908	CATAGCACCAACCCC[A/G]GAACAGGTAAACGAG	10043
rs371534879	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35321059	GACGGGGCATCAGAA[C/T]ACTATGCTAGCTGGG	10043
rs371595266	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35320729	CTTCTTTGGATCTCC[C/T]CGCAAGGTGGGGAGG	10043
rs371627770	snp	C/T	0.0185938	0.0946107	intron-variant	TOM1	GRCh38.p7	22:35310040	TTAATAAAAATTTCA[C/T]ATAGTCACTGAGTAC	10043
rs371642949	snp	A/G			intron-variant, downstream-variant-500B	TOM1, MIR3909	GRCh38.p7	22:35335985	ATGCTCTTCACACAG[A/G]GAAGGGGGCAGGATG	10043
rs371646700	snp	C/G			intron-variant	TOM1	GRCh38.p7	22:35316424	AGAAAACAGGCCATG[C/G]GGCACCTCCCTTTCC	10043
rs371665132	snp	A/G	9.93016e-05	0.00704563	intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334497	GTTCGGGTGGCTCTC[A/G]GGGTTCTGGAACCCG	10043
rs371740258	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1	GRCh38.p7	22:35326157	TTAGGTAGTCTATAA[A/G]TGGTAGCTGCTGTCA	10043
rs371750946	snp	A/C			intron-variant	TOM1	GRCh38.p7	22:35331259	CACCACCACACCCAG[A/C]TAATTTTCTTTTCTT	10043
rs371761805	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35306058	AAATGAATGAGAATG[A/G]CTGTGCATAAATAAA	10043
rs371767152	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35310837	CCTGGGAGAGAGAGA[C/T]GTAGAAACAAAGAGA	10043
rs371788468	snp	C/T	0.000275962	0.0117433	intron-variant	TOM1	GRCh38.p7	22:35327439	CTCCTGCCCAGCTGC[C/T]CACATGCATTCTTTC	10043
rs371791801	snp	A/G	3.31186e-05	0.00406918	missense, nc-transcript-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35323094	GCCAGCCAGGACTTC[A/G]TGGAGAGTGTGCTGG	10043
rs371835133	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35302330	TTTCTTTTTCTTTTT[C/T]TTTTTTTTTTTTTTT	10043
rs372011654	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35330671	GCCCCTCCTTCCAGC[C/T]GCCCTGTATCTCCTT	10043
rs372092119	snp	C/T	1.80367e-05	0.003003	intron-variant	TOM1	GRCh38.p7	22:35322983	GGTTCTGAGCACCTC[C/T]TCTCCTCTGACCAAG	10043
rs372131346	snp	A/G	0.00398564	0.0444627	intron-variant	TOM1	GRCh38.p7	22:35344324	CTGCCAGGCATGGGC[A/G]TGGGGCACCGTGCTG	10043
rs372166863	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35302312	AATTTCTTTTTTTTT[C/T]TTTTTCTTTTTCTTT	10043
rs372197038	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35344457	GGCCAGCCCAGCTTC[C/T]GCAGCTCCTCTGTGC	10043
rs372211207	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35315918	CCAGTGCCTGGAACC[A/G]GCTTGGCTTACAAAT	10043
rs372267431	in-del	-/TTCA	0.00159617	0.0282053	intron-variant	TOM1	GRCh38.p7	22:35310704	AATACAGCCTCATCT[-/TTCA]TTCAGTCATTCAGCA	10043
rs372382571	snp	A/G	0.000116056	0.00761674	intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334307	GGATGGGTCTTTCAC[A/G]TGGCCTTTCTGTCCC	10043
rs372403364	snp	C/T	0.000153988	0.00877328	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35327364	CCCACCCAGGCCGAG[C/T]CCGCAGACCTGGAGC	10043
rs372488046	snp	A/G	3.33539e-05	0.00408361	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35347166	GCCCAGCGCCCCGGA[A/G]GAAGACCCAGGAGAA	10043
rs372622725	snp	G/T			intron-variant	TOM1	GRCh38.p7	22:35328061	GACAGAGCGCTTCGT[G/T]TAACTGTTCGAGTTC	10043
rs372649109	snp	C/T	0.000133605	0.00817219	intron-variant	TOM1	GRCh38.p7	22:35346991	GTCCCCGCCCCTGCC[C/T]GCCCTCTCCTTTCCC	10043
rs372659429	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35314304	TCCTCCTCTTCCTCT[C/T]CCCTTTCTCGTTTAG	10043
rs372700472	snp	C/T	7.90233e-05	0.00628533	intron-variant	TOM1	GRCh38.p7	22:35299996	GTGAGTCCCTGGAGC[C/T]CCCCACAGCTCCGCC	10043
rs372713079	snp	C/T	0.00398564	0.0444627	intron-variant	TOM1	GRCh38.p7	22:35341825	TCACTGATTTATCTC[C/T]GATAACCTGGGAGAT	10043
rs372823285	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35311708	ACAAGTTTGGAGCAC[A/G]CAGGCCTGGCTTTGC	10043
rs372827998	snp	A/G	0.00159617	0.0282053	intron-variant	TOM1	GRCh38.p7	22:35338863	CACCCACTGGGTGCC[A/G]TTGTGGGCCAAGCAC	10043
rs372832295	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35340907	GGCAAGGTGGAGGAC[A/G]CTGGGGTGGGCCATC	10043
rs373005018	in-del	-/TCT	0.000856221	0.0206731	intron-variant	TOM1	GRCh38.p7	22:35333022	CCACCAAGGTAAAAG[-/TCT]TCTTTTCTGTGACTA	10043
rs373034912	snp	C/T	6.59554e-05	0.00574224	synonymous-codon, intron-variant, nc-transcript-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35323525	GTTCCGCAGCTCGCC[C/T]GATCTGACAGGTGTG	10043
rs373082834	in-del	-/GT	0.00159617	0.0282053	intron-variant	TOM1	GRCh38.p7	22:35341474	GGAGAGTGAGTGGAG[-/GT]GTGTGTCTCCCTCCT	10043
rs373113007	snp	A/G	0.000164731	0.00907405	utr-variant-5-prime, missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35317906	GGCTCCCTGCAGAGC[A/G]AGGACTGGGCCCTCA	10043
rs373191919	snp	A/G	0.000950975	0.0217849	intron-variant	TOM1	GRCh38.p7	22:35346982	AAGGTAGTAGTCCCC[A/G]CCCCTGCCCGCCCTC	10043
rs373196492	in-del	-/CATT	0.00835141	0.0640778	intron-variant	TOM1	GRCh38.p7	22:35329978	GGCTGGAGGCCCGTG[-/CATT]AGAGATGGCCTCACT	10043
rs373259061	snp	C/T			synonymous-codon, nc-transcript-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35338747	CAAGCAACAGACGGC[C/T]TGGCTGGAGCCCTGG	10043
rs373263325	snp	A/G	0.0287284	0.116357	upstream-variant-2KB	TOM1	GRCh38.p7	22:35297601	GCTGGGACTACAGGC[A/G]CCCACCACGGCGCCC	10043
rs373334938	snp	C/G	0.000105387	0.00725826	intron-variant	TOM1	GRCh38.p7	22:35330529	CTGCCCCAACCCTCT[C/G]CCTTCCCTTCCTCCC	10043
rs373378851	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35328919	AAGAAATAATTGACC[A/G]ATCTTAAAAATGAAA	10043
rs373387929	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35318090	AAGTCTGACCCAACC[C/T]GCTTGGCTGCAGAGG	10043
rs373417436	snp	A/C	6.77117e-05	0.00581818	intron-variant, missense, nc-transcript-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35299974	TCTCCAGTGGGACAG[A/C]GCATCGGTGAGTCCC	10043
rs373453526	snp	C/T	1.64912e-05	0.00287147	intron-variant	TOM1	GRCh38.p7	22:35345803	TGTTGGGGCCCACTC[C/T]TCACCCACACAGCAG	10043
rs373497265	snp	A/G	4.97566e-05	0.00498757	intron-variant	TOM1	GRCh38.p7	22:35323474	CTGTGGTTACCGGCT[A/G]TGTCCCCTTGTCCCC	10043
rs373515910	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35333658	TGCAAGGTGGGGCAC[C/T]CGGGGTCACTGCCCC	10043
rs373562278	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35339193	AAAATTAGCTGGGCG[C/T]GGTGGCACATGCCTG	10043
rs373602081	snp	C/T	0.000145693	0.00853377	intron-variant	TOM1	GRCh38.p7	22:35323938	GCCTGGGGTCAGAAC[C/T]GTCAGGTCCAGGCAG	10043
rs373641250	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35341538	CGGAACCAACACACC[A/G]CGAGCCTGCTGTAGG	10043
rs373649990	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35324302	AGCTTTCATTTGAGC[C/T]GGGCATGGTCACGTG	10043
rs373746058	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35318682	TCCAGCAATAAGCCC[A/G]AGTCCCTGGAGGGAG	10043
rs373781855	snp	C/T	8.43747e-05	0.00649463	intron-variant	TOM1	GRCh38.p7	22:35333368	GAACGAAGCTGCAGA[C/T]AGCGGGGATGATCAG	10043
rs373804111	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35305428	GCACGTTGGGAGGCC[A/G]AGGCGGGTGGATCAC	10043
rs373904125	snp	A/G	0.000153988	0.00877328	intron-variant	TOM1	GRCh38.p7	22:35332977	TGTCTTTTCTGTCTT[A/G]TAGGTTTGAACGGTT	10043
rs373916281	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35313892	CTGGAAGACAAGAGC[A/G]CAGCTGCTACCCGGA	10043
rs374004180	snp	C/T	0.000166561	0.0091243	synonymous-codon, nc-transcript-variant	TOM1	GRCh38.p7	22:35347089	AGAACGGGCCAAAGC[C/T]GCGGACCGATTGCCC	10043
rs374035810	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35330045	AGCACTTTGGGAGGC[C/T]GAGGCAGGCAGATCG	10043
rs374037100	snp	A/T	0.0107246	0.0724382	intron-variant	TOM1	GRCh38.p7	22:35330910	TAGGATAATAATCTT[A/T]ATTAAATGGGTAGCT	10043
rs374092477	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35302318	TTTTTTTTTCTTTTT[C/T]TTTTTCTTTTTCTTT	10043
rs374115421	snp	A/G	9.88452e-05	0.00702942	missense, nc-transcript-variant, intron-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35321976	CCAAAGATGCCCTCC[A/G]AGCAGTAAAGAAGAG	10043
rs374166505	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35330005	CCTCACTTGGCCAGG[C/T]GCGGTGGCTCACGCC	10043
rs374257520	snp	A/G/T	0.000383771	0.0138478	intron-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35338694	GCAGCATCCAATGGC[A/G/T]TGGTGGTCTCTCTTT	10043
rs374300103	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35301807	AAAGGACCCCTGCCC[C/T]CCCCGGACACACACC	10043
rs374307816	in-del	-/TCCTTGTGGA			intron-variant	TOM1	GRCh38.p7	22:35342567	TGGGATCCTTGTGGA[-/TCCTTGTGGA]GAGAGTTGAGAAGCT	10043
rs374383947	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35309567	GAGAATCGCTTGAAC[C/T]GGTGAGGCGGAAGTT	10043
rs374453651	in-del	-/AA	0.474	0.111014	intron-variant	TOM1	GRCh38.p7	22:35312244	ACAAGACTCCGTCTC[-/AA]AAAAAAAAAAAAAAG	10043
rs374487892	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1	GRCh38.p7	22:35323291	TCCGCTTCTCATTTC[A/G]GGGCGTCTCGGTTGT	10043
rs374494441	snp	A/G	0.00597247	0.0543191	intron-variant	TOM1	GRCh38.p7	22:35329669	GTATGCTTTGGTTGC[A/G]AAAATCACAGCATAC	10043
rs374495709	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35304680	AGACGGGGTTTCACC[A/G]TGTTAGCCAGGATGG	10043
rs374574167	snp	C/T	0.00199481	0.0315187	intron-variant	TOM1	GRCh38.p7	22:35325301	TATCATTTGAACTCA[C/T]TCTCACCCTAACCTA	10043
rs374599021	snp	A/G			upstream-variant-2KB	TOM1	GRCh38.p7	22:35298075	AAGTTCATGCTAAAC[A/G]TAACTCCATATGACC	10043
rs374642723	snp	A/G	3.30846e-05	0.00406709	intron-variant	TOM1	GRCh38.p7	22:35318012	CGGCCATCCCACCAC[A/G]CAGCACACTCCTGCA	10043
rs374756692	snp	A/G	0.000153988	0.00877328	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35323790	TCAACTCAGAGACAC[A/G]ATCAGGACAGGATTC	10043
rs374774753	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35344458	GCCAGCCCAGCTTCC[A/G]CAGCTCCTCTGTGCC	10043
rs374837673	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1	GRCh38.p7	22:35310337	AGACGGGTGGATCAC[A/G]AGGTCAAGAGATCGA	10043
rs374885646	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35343256	CCCACCACACACACC[C/T]CCACACACCTCCACT	10043
rs374900298	snp	C/T	1.64776e-05	0.00287028	synonymous-codon, nc-transcript-variant	TOM1	GRCh38.p7	22:35327312	GATGGTGAGTGGGAA[C/T]GTGAGGGTGATGTCG	10043
rs374904693	snp	A/T	3.30169e-05	0.00406293	intron-variant	TOM1	GRCh38.p7	22:35317850	CAGGACCCCCTCATG[A/T]CTTTATGACTCCTGG	10043
rs374947714	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35326754	CTAGGAGGAGAGAGA[C/T]GGCGGGATCCCAGTC	10043
rs374981805	snp	C/G			intron-variant	TOM1	GRCh38.p7	22:35304160	ACTCAAGGTCAGAAT[C/G]CAGACCCAGGTCTTC	10043
rs375038627	snp	A/G	4.98004e-05	0.00498976	missense, nc-transcript-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35323148	AACCCACCCACCATC[A/G]TGCATGACAAAGTGC	10043
rs375040017	snp	A/G	1.64727e-05	0.00286986	intron-variant	TOM1	GRCh38.p7	22:35333040	TCTTTTCTGTGACTA[A/G]ATCAGGCCCTGTTCA	10043
rs375067562	snp	A/C/G			intron-variant	TOM1	GRCh38.p7	22:35320522	CTTAGTTCCTCCAAG[A/C/G]CATCAAGCTCCTCTG	10043
rs375089799	snp	A/G/T	0.000200507	0.0100109	intron-variant	TOM1	GRCh38.p7	22:35346992	TCCCCGCCCCTGCCC[A/G/T]CCCTCTCCTTTCCCC	10043
rs375112395	snp	C/G	1.68462e-05	0.00290221	intron-variant	TOM1	GRCh38.p7	22:35323207	AGGGCAGGGCACGGC[C/G]AGGAAGAGCTGTCAG	10043
rs375225284	in-del	-/C			intron-variant	TOM1	GRCh38.p7	22:35302330	TTTCTTTTTCTTTTT[-/C]TTTTTTTTTTTTTTT	10043
rs375240421	snp	A/G	0.00011548	0.00759781	intron-variant	TOM1	GRCh38.p7	22:35345818	CTCACCCACACAGCA[A/G]GAGGACCCGTTGTTC	10043
rs375280634	in-del	-/CA			intron-variant	TOM1	GRCh38.p7	22:35343463	ACACCTACACACACA[-/CA]TTCATACACCTACAC	10043
rs375322570	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35339245	CTAAAGCAGGAGAAT[C/T]GCTTGAACCCAGATG	10043
rs375466877	snp	A/G	0.00071409	0.0188821	intron-variant	TOM1	GRCh38.p7	22:35322075	CTGTGGCAGGACTAC[A/G]GTCCACTGAAAGTCA	10043
rs375495087	snp	C/T			intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334511	CGGGGTTCTGGAACC[C/T]GGTTTTATGGTGGCA	10043
rs375520893	snp	A/G	0.00199481	0.0315187	intron-variant	TOM1	GRCh38.p7	22:35340206	AGTCCAGGGAGTCCG[A/G]GGGAGTGAGGGTGGT	10043
rs375581604	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35343414	CACACACAGCCCTAC[A/G]CACACCACACACACA	10043
rs375597002	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35314809	CACCTGCGCCACAGC[A/G]TCAGCGGCTGCCCCG	10043
rs375711882	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1	GRCh38.p7	22:35332098	TCATTTTTTGTGTCT[C/T]TCTCCATCAAAAGAC	10043
rs375718275	snp	A/C/T	3.29811e-05	0.00406075	intron-variant	TOM1	GRCh38.p7	22:35323649	AGAGAACTGCCGTAC[A/C/T]GGGAACCAAGGGAAG	10043
rs375781850	snp	C/T	0.000115452	0.00759687	intron-variant	TOM1	GRCh38.p7	22:35345707	GGGCACTGCCTTACC[C/T]TCTGCCCTTCCTTCC	10043
rs375817161	snp	A/C			intron-variant	TOM1	GRCh38.p7	22:35300133	CCCAGCTTTCCTCCC[A/C]CTCTTGATTGACAAG	10043
rs375818696	snp	A/G	8.41489e-05	0.00648594	intron-variant	TOM1	GRCh38.p7	22:35346888	GGCTGACCGTACTGG[A/G]GGCCCGGCTAACCTC	10043
rs375831359	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35322404	TTTGGTGCTCTGGCA[A/G]ATGAATGTAAAATAA	10043
rs375837120	snp	C/T	0.00159617	0.0282053	intron-variant	TOM1	GRCh38.p7	22:35321477	AATCTCGGCTCACTG[C/T]AACCTCTGCCTCCTG	10043
rs375840046	in-del	-/TACAAA			intron-variant	TOM1	GRCh38.p7	22:35301285	ATAAAAATATACACA[-/TACAAA]CATACATATACATAC	10043
rs375882814	snp	A/G	0.000307953	0.0124049	intron-variant	TOM1	GRCh38.p7	22:35327434	GATGACTCCTGCCCA[A/G]CTGCCCACATGCATT	10043
rs375908275	snp	C/T	1.80788e-05	0.0030065	intron-variant	TOM1	GRCh38.p7	22:35300018	AGCTCCGCCCCGGTG[C/T]TCCGCACCCAGCTTC	10043
rs376075534	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35314063	AAATATTGCCAGGTT[C/T]CTGTGGGTTTAAAAT	10043
rs376078810	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35307572	CTCCTCAAGGGACAC[A/G]GGAAACTTAGAAGTT	10043
rs376101206	snp	A/G			intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35335290	CTTAGAGGTCATTCT[A/G]GTGTCTTTTGGAACT	10043
rs376157405	snp	A/G	1.66189e-05	0.00288256	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35346939	TCCCAGGGTAATGAT[A/G]CGGAAGAGCCTAAGG	10043
rs376245725	snp	A/C/G	0.00159617	0.0282053	intron-variant	TOM1	GRCh38.p7	22:35333318	TGACAGATCCCTGGG[A/C/G]AAAGCCTGCAAGCCA	10043
rs376289758	in-del	-/A			intron-variant	TOM1	GRCh38.p7	22:35314542	TTTAAAAGCCACTTA[-/A]CTTGCCTTTCCAAAA	10043
rs376457227	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35341315	ACGCTTCGCAGTACC[A/G]CCATGTCCTCATCCC	10043
rs376457954	snp	C/T	0.000676595	0.0183804	intron-variant	TOM1	GRCh38.p7	22:35317997	GGTTGGGGGCAGAGA[C/T]GGCCATCCCACCACG	10043
rs376490654	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35308900	TGGTTTATGGTTAAA[A/G]AAAATACAGGGGAGA	10043
rs376495359	snp	A/C			intron-variant	TOM1	GRCh38.p7	22:35309127	TTGATATGTTTGTAG[A/C]GGATAGCATTTATTT	10043
rs376525660	in-del	-/GTCAT			intron-variant	TOM1	GRCh38.p7	22:35342924	CACACACCTCCACAC[-/GTCAT]ACCTCCACTCATACA	10043
rs376543972	snp	A/C			intron-variant	TOM1	GRCh38.p7	22:35346533	TCAGCCTTTCCCCCC[A/C]AGGGGTGAGGACCAC	10043
rs376544852	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35346804	CCTGGGTGGTGGGGG[C/T]GTGCAGAGCCTGAGC	10043
rs376546070	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35329032	GCGATCTCGGCTCAC[C/T]GCAGCCTCTGCCTCT	10043
rs376589424	snp	C/T			intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35333735	CCATCCTAGGATTGG[C/T]CCTCTACACTGAATT	10043
rs376676238	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35315005	TTAAAATATTATTAT[C/T]GTGGAAGGGCATGCA	10043
rs376973081	snp	G/T	8.23621e-05	0.00641672	intron-variant	TOM1	GRCh38.p7	22:35333046	CTGTGACTAGATCAG[G/T]CCCTGTTCATGGGAA	10043
rs377002453	snp	C/T			intron-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35337411	TGACGCCCCACCTCC[C/T]CCGCCACTGGCTTTA	10043
rs377022468	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35338314	CAGCAGAATGGAATC[C/T]CCCATTCAAATACGA	10043
rs377171728	snp	C/T	6.58892e-05	0.00573936	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35332988	TCTTGTAGGTTTGAA[C/T]GGTTCCGAACAGGCC	10043
rs377225709	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35303659	CACACCACCATGCCC[A/G]GCTAATTTTTGTATT	10043
rs377229955	snp	A/G	0.000798403	0.0199641	downstream-variant-500B	TOM1	GRCh38.p7	22:35348457	TCGATGTATAGATGC[A/G]GAGACTAGGACTCCA	10043
rs377231744	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1	GRCh38.p7	22:35330678	CTTCCAGCCGCCCTG[C/T]ATCTCCTTTCCAGGG	10043
rs377233068	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35331303	TTTTGCAGAGACAGG[A/G]GTCTCACTGTGTTGC	10043
rs377235211	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35311093	CAGAAGCCTGAGGAG[A/G]GTGATGGGGTGGCTG	10043
rs377284505	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334892	GGAGCAGGGAAGTTT[C/T]CTGATAAATCCTCAG	10043
rs377287426	snp	C/G	0.00119737	0.0244387	intron-variant	TOM1	GRCh38.p7	22:35328439	CGCTCACGTAATCCT[C/G]ACCACCCCCATTTTC	10043
rs377290270	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35345142	CCCCATCTGTAGCAC[C/T]GCCCCTCTGGGTCTA	10043
rs377292047	snp	C/T	0.00318978	0.0398085	intron-variant	TOM1	GRCh38.p7	22:35328238	CAGTGAATACACAAA[C/T]TTGAAACCCAGTAAG	10043
rs377296197	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35326613	CCCAGTCCACTAGGA[A/G]GAGAAAGAGGGCAGA	10043
rs377303679	snp	C/T	0.000148389	0.00861234	missense, nc-transcript-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334417	ATGTTTGCGCTGACA[C/T]GGGGCAGCTCACTGG	10043
rs377307531	snp	A/G	0.00358779	0.0422022	intron-variant	TOM1	GRCh38.p7	22:35346301	AGACTCAGCTTCTCC[A/G]TCCAGGGCTCCTACC	10043
rs377345112	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35342782	CACATCTACACCCAC[C/T]ACACACACCTCCACA	10043
rs377489139	snp	C/T	3.31098e-05	0.00406864	intron-variant	TOM1	GRCh38.p7	22:35323489	GTGTCCCCTTGTCCC[C/T]TCTCAGTCCTGGGCT	10043
rs377547348	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35318472	AGCACTGGCGTTTGC[C/T]GGGCGTTTCTGGTGT	10043
rs377560801	snp	A/G	1.64781e-05	0.00287033	missense, intron-variant, nc-transcript-variant	TOM1	GRCh38.p7	22:35323586	GGCCTGGAGTTCCCC[A/G]TGACTGACCTGGACA	10043
rs377588320	snp	A/C	0.0123036	0.0774623	intron-variant	TOM1	GRCh38.p7	22:35343174	CCACACACCACACCT[A/C]CACACACCACACCTC	10043
rs377589164	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35322834	CTGCCCACCCTAGGC[C/T]GTGCCCTCCAGTAAA	10043
rs377589869	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35324318	GGGCATGGTCACGTG[C/T]GTCTGTGATCTTAGC	10043
rs377607335	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35314681	ACTGAGAGGCCTGCC[A/G]GTGGAGCTCAGGGAG	10043
rs377620586	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35318896	CAGGGTTCCTCTCAG[C/T]CCGGGAGGGCTTTGC	10043
rs377627754	snp	C/T	0.000187899	0.00969094	intron-variant	TOM1	GRCh38.p7	22:35300023	CGCCCCGGTGCTCCG[C/T]ACCCAGCTTCGGTCC	10043
rs377656904	snp	C/G			intron-variant	TOM1	GRCh38.p7	22:35303056	TGACATCCCTCAGAT[C/G]GTGATTCTAATGATG	10043
rs377691974	in-del	-/G	0.00279162	0.0372561	intron-variant	TOM1	GRCh38.p7	22:35338897	CCCAGCACGTCCACA[-/G]GCCCTTCCTCGTTTG	10043
rs386395321	in-del	-/GT			intron-variant	TOM1	GRCh38.p7	22:35314219	TGGTCTGGGCAGATG[-/GT]TCCCACAGCCTCCCA	10043
rs386820992	multinucleotide-polymorphism	AA/TC			intron-variant	TOM1	GRCh38.p7	22:35300101	AGGCTGGCGTGTAGC[AA/TC]TCCGACCTGGCTCCG	10043
rs386820993	multinucleotide-polymorphism	GA/TG			intron-variant	TOM1	GRCh38.p7	22:35305729	AGGGCTCCAAGGGCA[GA/TG]GTGTGTGGTTACAGG	10043
rs397703691	in-del	-/AAAAAAAAAAAAAA	0	0	intron-variant	TOM1	GRCh38.p7	22:35321001	GAAAAAAAAAAAAAA[-/AAAAAAAAAAAAAA]CTTGAATGGAAGGGT	10043
rs397717757	in-del	-/C			intron-variant	TOM1	GRCh38.p7	22:35306750	ATCATTCCTGGGACC[-/C]CAGTCTAAGTTAGTA	10043
rs397744998	in-del	-/TATAT			intron-variant	TOM1	GRCh38.p7	22:35301320	CACATACATATATAT[-/TATAT]GTATTTACACACACA	10043
rs397777435	in-del	-/C	0	0	intron-variant	TOM1	GRCh38.p7	22:35306751	TCATTCCTGGGACCC[-/C]AGTCTAAGTTAGTAG	10043
rs397783649	in-del	-/T			intron-variant	TOM1	GRCh38.p7	22:35306154	TTCAGCTTTTTTTTT[-/T]CCCAACTATTTAAAA	10043
rs397803533	in-del	-/C	0.49395	0.0546662	intron-variant, upstream-variant-2KB	TOM1	GRCh38.p7	22:35299684	GCGCTTCCCGGGCCC[-/C]GACCCCAGACCCTAC	10043
rs397828441	in-del	-/GT	0	0	intron-variant	TOM1	GRCh38.p7	22:35314220	GGTCTGGGCAGATGT[-/GT]CCCACAGCCTCCCAA	10043
rs397831668	in-del	-/AAAT	0	0	upstream-variant-2KB	TOM1	GRCh38.p7	22:35297396	AATAAATAAATAAAT[-/AAAT]CCATATACTTCCATT	10043
rs397832065	in-del	-/GGCGCCCACCAC			upstream-variant-2KB	TOM1	GRCh38.p7	22:35297610	ACAGGCGCCCACCAC[-/GGCGCCCACCAC]CACGCCCAGCTAATT	10043
rs397832066	in-del	-/G			intron-variant	TOM1	GRCh38.p7	22:35302464	CCTCAGCCTCCCAAG[-/G]TAGCCGGGATTACAG	10043
rs397832067	in-del	-/T			intron-variant	TOM1	GRCh38.p7	22:35308290	Ctttttttttttttt[-/T]cttttttttttgaga	10043
rs397832068	in-del	-/T			intron-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35336958	TTTTTTTTTTTTTTT[-/T]GAGCCGGAGTCTCGC	10043
rs398037017	in-del	-/A	0	0	intron-variant	TOM1	GRCh38.p7	22:35342149	TATCTCAAAAAAAAA[-/A]GAAACAGAATCAAGT	10043
rs398081756	in-del	-/C			intron-variant, upstream-variant-2KB	TOM1	GRCh38.p7	22:35299683	CGCGCTTCCCGGGCC[-/C]CGACCCCAGACCCTA	10043
rs527275590	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334220	TTCCCCCACCCACAC[A/G]TGCCACTTCCCCAGC	10043
rs527286460	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35340523	AGGCCGAGGTGGGCA[G/T]ATCACTTGAGGTCAG	10043
rs527305954	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	TOM1	GRCh38.p7	22:35298521	CACTGCAATCTCTGC[C/T]CCCCTGGGTCCAAGC	10043
rs527321630	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35339937	GGACCCTAAAGCAGC[A/G]GGGAGAAATGCGAGG	10043
rs527466689	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35322941	CGGGCCTCCTCTCTG[A/G]GACACAGGAGGAGCC	10043
rs527593511	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35328305	CACGCCCCAAGCCAA[C/G]GCCATGAGATGTGAG	10043
rs527598163	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334671	GGGGAGGGGGAGCCT[A/C]ATGACCCACTGTATG	10043
rs527755017	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35311847	TCTTCACTGAATGAT[A/G]GCTGTCATTGTTCTC	10043
rs527815449	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35317380	AGTTAGTAAAGACGG[A/G]GCTTCACCATGTTGG	10043
rs527818133	snp	A/G	0.00478085	0.0486577	intron-variant	TOM1	GRCh38.p7	22:35308558	AAGTGCTAGGATTAC[A/G]GGCATGAGCTACCAC	10043
rs527879044	snp	A/G	0.000798403	0.0199641	intron-variant, nc-transcript-variant	TOM1, MIR3909	GRCh38.p7	22:35335681	TGGGGAGCAGGCTCC[A/G]GGGGACAGGGAAAAG	10043
rs527880242	snp	A/G	0.00438332	0.0466095	intron-variant	TOM1	GRCh38.p7	22:35322256	AGCATGGGAACAGAC[A/G]CTTACATCACTCCAG	10043
rs527922468	snp	A/G	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35335125	GGGAGAACTGGCCCC[A/G]TACAGGCTTGTAAGA	10043
rs527925032	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35341756	GCCCGCCCACAGGGA[A/G]GAAACGCACCACACA	10043
rs527947014	snp	C/T	0.000136008	0.00824534	intron-variant	TOM1	GRCh38.p7	22:35321694	ATGAGCCACCGCGCC[C/T]GGCCAGGTTCTGCAC	10043
rs527965628	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35306690	CACTTCCTGCCAGAC[A/G]GGAAGTCTCTGTAAT	10043
rs528011988	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	TOM1	GRCh38.p7	22:35348058	TTTGGGCAGGGCTGG[A/G]GGCCATCCGAGAGGT	10043
rs528062097	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35324955	TGGCACCCTGGGCAT[A/G]TCACTTCCTTCCTCC	10043
rs528067636	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35318645	CTAGGTCTTTGTCCT[C/T]GAAGGTGCTCTGTTA	10043
rs528146697	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35324094	GGTCCATTCACTTGC[C/G]CAGAGCACACAGTCA	10043
rs528160344	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35330711	AGCGCTGCTGCCTGT[A/G]CCCAAGTCCAGCCCT	10043
rs528184443	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35330228	CACAGCTTGCAGTGA[A/G]CCAAGATCGCACCAC	10043
rs528196839	snp	C/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	TOM1, MIR3909, MIR6069	GRCh38.p7	22:35336244	GTCAGGCGTGGACCT[C/G]AGCATCCATTTCGTC	10043
rs528270956	snp	A/C	0.00119737	0.0244387	intron-variant	TOM1	GRCh38.p7	22:35319876	CCCTTCCACCGCAGG[A/C]CTGACCGCCTCCATA	10043
rs528278997	snp	G/T	0.00438332	0.0466095	intron-variant	TOM1	GRCh38.p7	22:35307641	AAGCCCTGAGGAGGG[G/T]AACTGGGCCTCGCTC	10043
rs528336744	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35319499	ATCATGGGCCCACAG[C/T]AGTGGCAAGGCCAGA	10043
rs528342094	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35313515	GTCATACTGACATTG[C/T]CTGGCTGCAAGGTCA	10043
rs528374589	snp	A/T	0.00159617	0.0282053	downstream-variant-500B	TOM1	GRCh38.p7	22:35348078	ATCCGAGAGGTGAGC[A/T]TCTGTAGATGGTGCA	10043
rs528396424	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35316884	TTACTGTGCTGGTAC[C/T]TTGCATGAATCATCA	10043
rs528398137	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35318963	GGAGTGCCCAGCTCT[A/G]AGCTGGAGGGAGGCT	10043
rs528502491	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35337112	TGGCTAATTTTTTGT[A/G]TTTTTAGTAGAGACG	10043
rs528512909	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35302488	ATTACAGGCACGCTC[C/T]GCCACACCCGACTAA	10043
rs528560916	in-del	-/T	0.271972	0.249033	intron-variant	TOM1	GRCh38.p7	22:35303505	CATTTTTATTATTTC[-/T]TTTTTTTTTTTTTTT	10043
rs528586663	snp	C/T	0.00159617	0.0282053	intron-variant	TOM1	GRCh38.p7	22:35343573	TACACACACCACACC[C/T]ACACTCATACACCTA	10043
rs528623827	in-del	-/A			intron-variant	TOM1	GRCh38.p7	22:35323386	GGGCAGATGTAGTTA[-/A]AAAAAAAAAAAAAAG	10043
rs528885689	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35344844	GCTAAGCTTTTGACA[C/T]CCCATTTCATCCTCA	10043
rs529026294	snp	A/G	0.00636936	0.0560724	intron-variant	TOM1	GRCh38.p7	22:35321012	AAAAACTTGAATGGA[A/G]GGGTAAATGGACAGA	10043
rs529050638	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35343827	ACCTACACATACACA[C/T]CTACATTCATACACC	10043
rs529067009	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	TOM1	GRCh38.p7	22:35297690	TAGCCAGGATGGTCT[C/T]GATCTCCTGACTTCG	10043
rs529084693	snp	C/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35333717	TGGATCTCAGAAATC[C/G]TACCATCCTAGGATT	10043
rs529136623	snp	A/G	0.00358779	0.0422022	intron-variant	TOM1	GRCh38.p7	22:35339062	CAGGCCGGGCGTGGT[A/G]GCTCACACCTGTAAT	10043
rs529196964	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1	GRCh38.p7	22:35345522	TCCAGCTGCTGGGAG[C/T]CTGGTCCCCTGCTTA	10043
rs529204805	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35338466	ATCCTGGTCATAGCC[A/G]TTGGTGGTCTTGGTC	10043
rs529224497	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35303301	TACTCTCCCTTTATC[C/G]TAGATCCTCAGGCCC	10043
rs529401000	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35327660	ATGGCACAAGTTTGA[C/T]GTGAGTTAAATAAGG	10043
rs529418558	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334197	CAGCAGGTGGCCTGC[C/T]TCGCGCATTCCCCCA	10043
rs529456751	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35346754	CCAAGGAAGGTCCTA[C/T]GGCTCAGGGAGGAGC	10043
rs529462908	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35307592	ACTTAGAAGTTGATA[A/G]AGCACTGCAAAGTGC	10043
rs529509508	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35317176	GTTACCAACTCAAAA[A/G]ATAATTCTTTTTTGC	10043
rs529619268	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35335067	AGCATAGGCACGTGG[C/T]CTGAGTGTGTCCACC	10043
rs529706448	snp	A/G	6.67445e-05	0.00577649	intron-variant, missense, nc-transcript-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35299972	GCTCTCCAGTGGGAC[A/G]GCGCATCGGTGAGTC	10043
rs529708970	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35322576	CAGCATTTATATCCA[G/T]GTGAATTGGCTTAAG	10043
rs529733440	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1	GRCh38.p7	22:35299449	TCAAACAGGAAGAGT[C/T]TTACCGGGACAAGGA	10043
rs529741924	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35340700	TGTGGTGAGCTGAGA[C/T]TGCACTACGACACTC	10043
rs529750012	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35300351	TCCCGCCGCCTGGGC[G/T]CTGGCCAGCTCCTTC	10043
rs529789593	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35305366	TGCCAGAGGGAAGAA[A/G]GAAACTGATGGCGGG	10043
rs529848327	snp	A/G	0.000798403	0.0199641	intron-variant, downstream-variant-500B	TOM1, MIR3909	GRCh38.p7	22:35335762	TGCACCAGGACCACC[A/G]CTGTGAAGGGCTAAG	10043
rs529918523	in-del	-/TCCA			intron-variant	TOM1	GRCh38.p7	22:35343257	CACCACACACACCTC[-/TCCA]CACACACCTCCACTC	10043
rs529982972	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35329392	AACCTGAATAAAGTC[C/T]GCAGTTTAGTTAATA	10043
rs530170422	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35341284	GCCTGGCACACACTA[C/T]GGTATTACGGCACTT	10043
rs530179920	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35323252	GCCCAGTGGAGAGTC[A/G]AGGCCATCGTGTTTG	10043
rs530180915	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35312828	CCAGCCCCTGGAGAG[G/T]TCAGGCTTTTGATCC	10043
rs530243631	snp	A/G	0.00279162	0.0372561	intron-variant	TOM1	GRCh38.p7	22:35318466	CTGAACAGCACTGGC[A/G]TTTGCCGGGCGTTTC	10043
rs530380495	snp	A/C	0.000399281	0.0141238	intron-variant, downstream-variant-500B	TOM1, MIR6069	GRCh38.p7	22:35336357	TGCCAGCTTGGTGTC[A/C]AGCCCGCTCCTCCCT	10043
rs530396583	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35301255	ACATACACACACACA[A/C]ACGCACACATATATA	10043
rs530423334	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35342729	ACACACCTCCACACA[C/G]CACACCTCCACCCAT	10043
rs530496267	snp	A/G	0.00438332	0.0466095	intron-variant	TOM1	GRCh38.p7	22:35319078	CTCCCTGATCTTGCC[A/G]AGGACTCATGAGAGT	10043
rs530604715	in-del	-/CAC	0.00636936	0.0560724	intron-variant	TOM1	GRCh38.p7	22:35343231	TACACACACCACACA[-/CAC]ATCTACACCCACCAC	10043
rs530639909	snp	A/G	0.00438332	0.0466095	intron-variant	TOM1	GRCh38.p7	22:35302127	GAATGCTACTAAATC[A/G]TAATACCTTAAAGCA	10043
rs530648097	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35343866	CACCCCTGCATATAC[A/C]ACCCCTACACACTCA	10043
rs530660368	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35331510	GGTATGGGAGAGGGC[C/G]CTTTGATGGCAGCCC	10043
rs530725164	snp	A/G	0.0138799	0.0821421	intron-variant	TOM1	GRCh38.p7	22:35344210	ACCCAGATGGGAGGC[A/G]GCTGCGGGAAAAGCC	10043
rs530790277	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35326734	GAGGGCGGGATCCCA[A/G]TCCTCTAGGAGGAGA	10043
rs530801468	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35320341	ACAAGAGCAGTCAGG[A/G]CAGCACTGAGTATAC	10043
rs530877444	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35332538	GTAGCTCCATAAAAC[A/G]AGATTAGAGATACAT	10043
rs531200954	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35345987	GCACAGTAGCCTCTC[A/G]GCTGCTTCCCAGAGC	10043
rs531277283	snp	A/G	0.00358779	0.0422022	intron-variant	TOM1	GRCh38.p7	22:35327021	TTCCAGCCACACGTG[A/G]TGGCTCATTCCGGTG	10043
rs531294887	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	TOM1	GRCh38.p7	22:35297794	TTATGATTCCACTTC[A/C]TGTTTGGGGGCATAT	10043
rs531330583	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35339102	TCGGGAGGCTGAGGC[A/G]GGTGGATCACCTGAG	10043
rs531366567	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35345662	CAGCTGCAGGGTGCT[C/G]AGCTGGCACGTCTTC	10043
rs531483720	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35309683	AACTGAGAGACCTGC[A/T]GGGTTTCCCTTTGAG	10043
rs531603336	snp	A/C	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334207	CCTGCCTCGCGCATT[A/C]CCCCACCCACACGTG	10043
rs531618442	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35317327	CCCAAGTAGCCAGGA[A/T]TACAGGCATGTGCCA	10043
rs531640004	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35333743	GGATTGGCCCTCTAC[A/G]CTGAATTCTCCATGG	10043
rs531683697	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35322835	TGCCCACCCTAGGCC[A/G]TGCCCTCCAGTAAAC	10043
rs531804636	snp	A/C	0.0126979	0.078662	intron-variant	TOM1	GRCh38.p7	22:35341253	GAAACCACAGGTGTA[A/C]TGTCCTCGGTATGGT	10043
rs531811766	snp	C/G	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35305862	GAAGGCAGAAGCCGG[C/G]GTGGGGAGGGCGACT	10043
rs531867437	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35322317	GACCTGTGGGTGACA[C/T]TGAAGCTCAGTAAAC	10043
rs531883796	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35328675	ACCCGCCCTGTCCCC[A/G]TGCTAAGGGCGATGA	10043
rs531930445	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35311671	GGCAGTCTTCACAGG[C/G]ACAGAGCAGAGTGGA	10043
rs531961266	snp	C/T	0.000461353	0.015181	missense, intron-variant, nc-transcript-variant	TOM1	GRCh38.p7	22:35323611	TGGACATGCTGTCAC[C/T]CATCCACACACCCCA	10043
rs531961398	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35330151	TAGCCAGGCGTGGTG[G/T]CAGACGCCTGTAGTC	10043
rs532005667	snp	C/G			intron-variant	TOM1	GRCh38.p7	22:35307312	TCCATGAAATCATGG[C/G]TTTGATGTTCGTGTT	10043
rs532011101	in-del	-/A	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35337310	TTCAGCCTTGCCCAC[-/A]ATGCGCCAAGCATGT	10043
rs532046220	in-del	-/C			intron-variant	TOM1	GRCh38.p7	22:35311594	CAAAAGTATGTAATG[-/C]CCCCCCTCTGCTCTG	10043
rs532132260	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35328683	TGTCCCCGTGCTAAG[A/G]GCGATGAGGAAATCC	10043
rs532277029	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35318521	TTGCTCAGTGCCAAG[G/T]AGCCCTGCCAAGGCA	10043
rs532315566	snp	C/T	0.00159617	0.0282053	intron-variant	TOM1	GRCh38.p7	22:35324032	TTCCTCACAGCAGCC[C/T]ACAGGGTATGTGTGG	10043
rs532343879	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35318889	GCCAGTGCAGGGTTC[C/T]TCTCAGCCCGGGAGG	10043
rs532398502	snp	A/G	0.000798403	0.0199641	intron-variant, downstream-variant-500B	TOM1, MIR6069	GRCh38.p7	22:35336454	AGCTCCTTATCAGCC[A/G]CTGTTTCTGCTCCAG	10043
rs532434923	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35342853	CACACCACACCTACA[C/T]ACTCATGCACCTACA	10043
rs532496544	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1	GRCh38.p7	22:35324006	TTTACCATCCACGGA[A/G]CCTCCACTTCTTCCT	10043
rs532505006	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35301951	CTTACTACTTAAAAA[G/T]AAACAAGTAAATAAA	10043
rs532659431	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35332667	CCTTACCTTTACTGC[A/G]TGCCATGCATTCCTA	10043
rs532686081	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35313416	TGCCCGTGGTGTGGC[A/G]TGTCTTTGGTGACTA	10043
rs532697170	snp	A/C	0.00119737	0.0244387	intron-variant	TOM1	GRCh38.p7	22:35307044	TTAGAAAAAAAAAAA[A/C]CCAAACCCTCAGTGT	10043
rs532729611	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35307658	ACTGGGCCTCGCTCC[C/T]GCTGGGGAAGGTAGA	10043
rs532823062	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35331626	CAGTGGCTCACACCT[A/G]TAATCCTAGCACTTT	10043
rs532858421	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35314133	AGGAAATCCACATGA[C/T]TCACCGCAATCCTGT	10043
rs532948386	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35314458	CACGGGGTGGGGGCG[A/G]GGGGTCCTTCTGCTC	10043
rs532979721	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35303229	AGATCACCCTTCAAA[C/G]TACAGGGCATCATCA	10043
rs533016193	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35320295	AGGAGCCTTCAGGGT[A/G]CAAGTGGGGGCCCTG	10043
rs533102408	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35326536	TTCAAGGTGGGGTAC[A/G]GGGCAAGGACTATCC	10043
rs533103196	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35308972	AGATGGATGGAACTT[C/T]CCACGCTGGGTCTGG	10043
rs533147250	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35338338	AATACGACCTCATAC[A/G]CAACCACAGTCTATA	10043
rs533196069	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35344789	TAAATAGGAACTGGC[C/T]TATTGGTTTCTTGAG	10043
rs533223715	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35327169	TGGGAGGTCGGCTCC[C/T]TGGTGCTGCACCCAG	10043
rs533312585	snp	C/G	1.64846e-05	0.0028709	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35345728	CCTTCCTTCCAGATC[C/G]CAGTCACCCAGGCCT	10043
rs533368149	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35316425	GAAAACAGGCCATGC[A/G]GCACCTCCCTTTCCT	10043
rs533467935	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35314350	CCACCCCGCAGAAAA[C/T]CTCCGTCTTCTGATT	10043
rs533643592	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35315951	CCGTGTAGCAAGCGA[A/G]GAGTCACCCACCCTC	10043
rs533673673	snp	A/C	0.00159617	0.0282053	intron-variant	TOM1	GRCh38.p7	22:35339272	GATGGTGGAAGTTGC[A/C]GGGAGCAGAGATTGT	10043
rs533913786	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	TOM1	GRCh38.p7	22:35297421	ACTTCCATTTCTGTT[G/T]CAATAGCTATATAGT	10043
rs533921668	snp	A/G	0.00318978	0.0398085	intron-variant	TOM1	GRCh38.p7	22:35314141	CACATGATTCACCGC[A/G]ATCCTGTTGTCCACA	10043
rs533933484	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	TOM1	GRCh38.p7	22:35298931	AGTGTGTAGGTGTCA[A/G]CAGACACACCACACA	10043
rs533983135	snp	A/T	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35310758	CATGGCCCAGGTCCC[A/T]TCTGGGGTAGACAGT	10043
rs534011633	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	TOM1, MIR6069	GRCh38.p7	22:35336490	ACCACAGCTGGCACC[A/G]TCACAGCCTTCCTGC	10043
rs534063893	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35311325	GCAGGTAACAGGAAA[C/T]GCAACCAGCAGAGTC	10043
rs534096006	snp	A/G	1.64749e-05	0.00287005	synonymous-codon, nc-transcript-variant, intron-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35321980	AGATGCCCTCCGAGC[A/G]GTAAAGAAGAGAATC	10043
rs534230644	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35346829	CTGAGCTGGGACCCA[G/T]TGCTGAGGTTCAGCG	10043
rs534234406	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35340240	CCTGGGGCCGAGGAG[A/G]CTAGAGGAGGCTCAA	10043
rs534260501	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1	GRCh38.p7	22:35299799	GGCGGGGCTTGTGGT[A/C]GAGCTTCGCGGTGCC	10043
rs534274438	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1	GRCh38.p7	22:35347648	CTGCCGAGCCTCTTG[C/T]CCCTTCCCTGCTCTG	10043
rs534296388	snp	G/T			intron-variant	TOM1	GRCh38.p7	22:35312991	TGAGACTGTTGGAAT[G/T]TGCAGGATGGGAGCG	10043
rs534308997	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35342379	GGGAGCAGGACTCTC[A/G]TCTCCCTCCACTCTG	10043
rs534368769	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35318183	GCTGCCACCCCACCC[C/T]GCCTCTCTTAGTGGC	10043
rs534442700	snp	A/G			intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334037	TCGACTACCCATCTG[A/G]TTACTGTCCTCCTGC	10043
rs534577689	snp	C/G			intron-variant	TOM1	GRCh38.p7	22:35314594	CACTGATGTTCCCTC[C/G]TCCAGGAGATGAGAG	10043
rs534619378	snp	C/T	0.0146672	0.084371	intron-variant	TOM1	GRCh38.p7	22:35341539	GGAACCAACACACCG[C/T]GAGCCTGCTGTAGGA	10043
rs534689495	in-del	-/T	0.00159617	0.0282053	intron-variant	TOM1	GRCh38.p7	22:35308589	AGCCAGCCTAGTTCC[-/T]TTTCTCTAGAGATCC	10043
rs534763516	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35316617	GCTTCCAGAACTCTG[C/T]AGCCGACTCCCGGCC	10043
rs534818490	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35300766	GACGCAGCCTCCCTG[A/G]GCCGAGGTTTCCTCA	10043
rs534829867	snp	C/G			intron-variant	TOM1	GRCh38.p7	22:35329225	CCTCCCCAAGTGCTG[C/G]GATTATAGGCACGAG	10043
rs534830631	snp	A/G	8.2778e-05	0.0064329	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35330440	GAGGAGCTGCTCATC[A/G]TCAATGACAATCTCA	10043
rs534879341	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35300204	TATGACAGCCAGTAG[A/G]TAAGGAGAGAGGGTG	10043
rs534896855	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35307852	TATAAACCCTGTAGT[A/G]GTTAACTTTATGTGT	10043
rs534932784	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	TOM1	GRCh38.p7	22:35348267	GAGGCCAGCTCCTGC[C/T]CTGCACAGAGCACAC	10043
rs535017716	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35326012	TGCAGGTTTTGGAAG[C/G]TGTCAGTGAACCATA	10043
rs535054290	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35330989	AAGATGGATCCCAGG[A/G]CAGCTCAGATGTCTC	10043
rs535165485	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35309055	AAAAATAGCTTCTGC[A/G]TATTTGTGATTTAAA	10043
rs535219117	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35314144	ATGATTCACCGCAAT[C/T]CTGTTGTCCACACCT	10043
rs535269762	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35320595	CTCTGCCCCCACTCC[C/T]CCCAGGTGGTCCTTC	10043
rs535275362	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35344919	ACGAGGGAAATCAGG[C/T]GCAGAGAAGTTAAGT	10043
rs535334819	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35309792	CATTGGTTTCATCCT[C/T]GTGCTTGCATTCTCA	10043
rs535334912	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35338913	GCCCTTCCTCGTTTG[A/G]CCGTCAGGTCGGTTC	10043
rs535353121	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35319271	TGGGAGGAACAGGCT[C/T]GGCGTCGGTCAGGTG	10043
rs535445863	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35315986	AGCCGGGGCACAGCC[A/G]TGAGGAGAGAGCCTC	10043
rs535470692	snp	A/G	0.00318978	0.0398085	intron-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35337270	ATCATGGGTTTCTGC[A/G]TGTTCTGGGGCTGGG	10043
rs535508405	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35315500	GGAACCCCCAAGGGC[A/C]GGGGTGTGGTACAAA	10043
rs535558246	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35344014	ACTCATACACCTACA[C/T]ACACACCTACACTCA	10043
rs535678470	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35339506	TAGAAGTGTGAGAGG[A/G]TATATTTAGGGAGCT	10043
rs535738231	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1	GRCh38.p7	22:35304124	CTAAGAGAAAGCATC[A/G]CTTTCCAGGGTTCCA	10043
rs535741501	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35332682	GTGCCATGCATTCCT[A/G]TTTTCTTTGCTGTTC	10043
rs535786647	snp	G/T	0.00023298	0.0107905	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35345773	ATCGAGCAGTGGCTG[G/T]CCACTGACGTGGTAT	10043
rs535799856	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35310611	AGGATTTCCACACAA[C/T]AGCTAGTAAGGGATC	10043
rs535870105	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35322371	GGCCGGCTGACTGAG[C/T]TGGGTGCTGCTCGGC	10043
rs535930262	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35328388	GCACTGGGCACTTCC[C/T]GTGTCCCGGGCTATA	10043
rs536011177	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35346857	GCGGGGCCCGAGCTG[C/T]AGCACCACTGCCCCA	10043
rs536082752	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35305493	GGTGAAACCCTGTCT[C/T]TACTAAAAATACAAA	10043
rs536173531	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35303684	TGTATTTTTAGTAGA[A/G]ATGGGGTTTCACCAT	10043
rs536174076	snp	A/C			intron-variant	TOM1	GRCh38.p7	22:35328529	AGTAGCAGAGCTGCG[A/C]TTTGAACCCGGGGGC	10043
rs536203554	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35342939	GTCATACCTCCACTC[A/G]TACACCTACACACAC	10043
rs536233072	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35323967	AGGTGGGCCACACAC[A/G]TCAGGGAGGGCCCCC	10043
rs536257727	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1	GRCh38.p7	22:35311220	CAGGTCCATGCCGTA[A/G]TTGTCCACCGCGGAG	10043
rs536323428	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35318363	TCTGCGAGCAAAAAC[A/G]GACTTCCATTTCCTT	10043
rs536347726	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35327942	ACTGGAGCAGAAGGG[A/G]CACTGAATTTGGCAA	10043
rs536360175	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35320915	TGAGCCCAGGAGTTC[C/T]GGGCTACAGCGAGCT	10043
rs536394063	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	TOM1	GRCh38.p7	22:35298536	CCCCCTGGGTCCAAG[C/G]AATTCTCATGCCTCA	10043
rs536443997	snp	C/G			intron-variant	TOM1	GRCh38.p7	22:35305024	GAAAAGTGAAAAAGT[C/G]AGAGAGAGCTGTCTT	10043
rs536460260	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35311970	AGAAGATGAGGGGAG[C/T]TCGGCTGGGCACGGT	10043
rs536587601	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35316836	TGTTTATTTTGGGCC[C/T]GTACCGTGCTGATAC	10043
rs536637218	snp	C/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35335176	TTCTTCAGCCTTTTG[C/G]CCACTGTGACCCCCA	10043
rs536652911	snp	A/T	0.00795532	0.062565	intron-variant	TOM1	GRCh38.p7	22:35300129	TCCGCCCAGCTTTCC[A/T]CCCACTCTTGATTGA	10043
rs536674361	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334864	CACTGTGTACCGCAT[A/G]GTAAGCCCTCCAGGA	10043
rs536761252	snp	C/G	0.00358779	0.0422022	intron-variant	TOM1	GRCh38.p7	22:35340827	AAGTCTTCGTGACCC[C/G]CAAGGGCACTCTCTC	10043
rs536770128	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1	GRCh38.p7	22:35347342	CCTCCTCTTTGAAGA[C/T]GGAGCTGCCCCAGCT	10043
rs536831253	snp	A/G	0.00358779	0.0422022	intron-variant	TOM1	GRCh38.p7	22:35324319	GGCATGGTCACGTGC[A/G]TCTGTGATCTTAGCT	10043
rs536839595	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35331206	GCTCAAGCAGTCCTC[C/T]CACCTCAGCCTGCCA	10043
rs536877028	snp	A/C	0.00159617	0.0282053	intron-variant, downstream-variant-500B	TOM1, MIR6069	GRCh38.p7	22:35336627	CTTTGTCCGCATCTT[A/C]GTCAGTGCTGCTGTA	10043
rs536889647	in-del	-/CCT	0.00119737	0.0244387	intron-variant	TOM1	GRCh38.p7	22:35331952	TGTGTGCCCATCACA[-/CCT]CCTCTGTATCTGTAA	10043
rs536912164	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35330294	AAAAAAAAAAAGAGA[C/T]GGCCTCACTCTGAGT	10043
rs536994119	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35300887	GCCTGGTACATGGCC[A/G]GTGCCATATAAAAAA	10043
rs537063040	snp	A/G			utr-variant-3-prime, nc-transcript-variant	TOM1	GRCh38.p7	22:35347599	CCCACACTGCCAGTC[A/G]AGGCCTGGCTGGAGG	10043
rs537097697	snp	C/G			intron-variant	TOM1	GRCh38.p7	22:35342756	CCATAGACCTACACA[C/G]ACACCACACACACAT	10043
rs537136295	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35330750	GTCACAGGTCACAGC[C/T]GAGAGCACGGCCCTG	10043
rs537153758	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35325424	GGACAAAATTATTAA[C/T]GCACTGCCCGTTTGC	10043
rs537199618	in-del	-/A/AA	0.495483	0.0473088	intron-variant	TOM1	GRCh38.p7	22:35309643	GTGAGACTCCATCTC[-/A/AA]AAAAAAAAAAAAAAA	10043
rs537369602	snp	A/G	0.00557542	0.0525036	intron-variant	TOM1	GRCh38.p7	22:35343023	CACACATCTACACCC[A/G]CCACACACACCTCCA	10043
rs537378404	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35320478	TCTTCAGCCCTCCCC[A/G]ACCTCCCCCACACTC	10043
rs537449541	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35319907	GCTCTAGCCCCCAGG[C/T]AGGCTCTGTCCCTAG	10043
rs537471524	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35338638	AGCCGTCAATCTGTG[C/T]CCCCCAGCCCGCTCC	10043
rs537640298	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35321900	CAACTCTCCAGGGTC[A/T]CTGGTGTTAGGTAAG	10043
rs537653510	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35309133	TGTTTGTAGAGGATA[G/T]CATTTATTTTGGTGC	10043
rs537709549	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35308490	AGTTTCACCATGTTG[A/G]CCAGGCTGGTCTTGA	10043
rs537833195	snp	C/T	4.98045e-05	0.00498997	synonymous-codon, nc-transcript-variant	TOM1	GRCh38.p7	22:35333439	GGCAGCTGACCTGAT[C/T]GACATGGGCCCTGAC	10043
rs537856594	snp	G/T	0.00279162	0.0372561	intron-variant	TOM1	GRCh38.p7	22:35311280	ACCTCACTCCTTAAA[G/T]AGGAATATTAATCAC	10043
rs537962495	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35337765	AACAGGAATCGCAGG[A/C]CTTTCCCTTTGTGAC	10043
rs537987585	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35316078	ACTCCTGACAGATAA[C/T]AGACAGCCGGCAGCA	10043
rs538041470	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334839	TCTCCACCCCCCGCC[C/T]CCCTCCCTGCACTGT	10043
rs538043632	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35328491	GGAGATCAGATAACA[C/T]GTCCAGGGTTATATG	10043
rs538101824	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1	GRCh38.p7	22:35321450	GTTGCCCAGGCTGGA[A/G]TACAGTGGCGTAATC	10043
rs538143209	snp	C/T	0.000399281	0.0141238	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35327283	CAGATTGGGAAGCTG[C/T]GCAGTGAGCTGGAGA	10043
rs538143927	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	TOM1	GRCh38.p7	22:35298722	TACAGGCGTGAGCCA[C/T]CACACCTTGCTTAAT	10043
rs538198443	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35339612	CAGAGAGGAATAAAA[A/G]AGCGGACCCTGGCCA	10043
rs538233298	snp	A/C			intron-variant	TOM1	GRCh38.p7	22:35306518	CCCAGGGTGAGCTTG[A/C]GTCAGACTGAATGGT	10043
rs538249711	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35317523	AAGGGAGAACATCTT[A/G]TCTACAGAAATGAAG	10043
rs538277790	snp	G/T			intron-variant	TOM1	GRCh38.p7	22:35328704	GAGGAAATCCCGGAG[G/T]CCTGACCTTGGAGGG	10043
rs538314000	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35330060	CGAGGCAGGCAGATC[A/G]TGAGGTCAGGAGATC	10043
rs538323306	snp	C/T	0.000116139	0.00761946	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35323141	CAAGAACAACCCACC[C/T]ACCATCGTGCATGAC	10043
rs538578622	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	TOM1	GRCh38.p7	22:35298035	TAAAAATAAATAAAT[A/C]AAGGTTAATGGAAGA	10043
rs538612585	in-del	-/CTAAGGG	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	TOM1	GRCh38.p7	22:35299527	GTGAGGTCCCAAGGA[-/CTAAGGG]CTATGACCCTAAGAG	10043
rs538634160	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35304009	TTGTGAGCAAACACC[A/G]TAATAACTCTGCCAG	10043
rs538691963	snp	C/T	0.000134542	0.00820079	intron-variant	TOM1	GRCh38.p7	22:35323203	GGACAGGGCAGGGCA[C/T]GGCCAGGAAGAGCTG	10043
rs538738172	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35301205	GTACTCCAGCCTGGA[C/T]GACGCAGGGAGAGCC	10043
rs538845751	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35306183	AAATATAAAGACCAT[C/G]TGTAGCTCGAGTACC	10043
rs538902276	snp	A/G	0.00358779	0.0422022	intron-variant	TOM1	GRCh38.p7	22:35313071	CTGGCCGGACACAGT[A/G]GGCAGTGGCTCACAC	10043
rs538967777	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35311993	GGCACGGTGGCTCAC[A/G]CCTGTAATCCCAGCA	10043
rs539024857	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35336800	GCCCAGGGGTCACCA[C/T]CCAGTGCAGGAGGTG	10043
rs539029207	snp	A/G	1.66255e-05	0.00288314	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35330366	TCAACCGCACGTGCC[A/G]AGCCATGCAGCAGCG	10043
rs539056979	snp	A/G	0.00119737	0.0244387	intron-variant, downstream-variant-500B	TOM1, MIR3909	GRCh38.p7	22:35335838	AGCATGCAACTCTGC[A/G]GAGGGTACTCAGAGC	10043
rs539068369	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35330017	AGGCGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC	10043
rs539117294	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35300692	GCCCAGGGCACCTGG[C/T]GCCTGTCTGCTGGTC	10043
rs539216650	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35319193	GGGAGCTTCATGGAC[A/G]TCGCAGCTGCAAGTC	10043
rs539281917	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35305341	ATATATAGGGACAGG[A/G]AAGGGTTGATGCCAG	10043
rs539308770	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35325172	AGGCCCATCACATCC[A/G]CGGAGCGTAAAGGTG	10043
rs539348468	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35324501	CAAAAAATAAAAAAC[A/G]TATGTACATTGTACC	10043
rs539395500	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1	GRCh38.p7	22:35302290	TGCGGTGGGACTCTA[A/G]AATGTGAATTTCTTT	10043
rs539397162	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35343925	TACACACACCACACA[C/G]ATCTACACACACCAC	10043
rs539489674	snp	A/C	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35343221	CACACACCCCTACAC[A/C]CACCACACACACATC	10043
rs539501722	snp	C/G	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35320497	TCCCCCACACTCAGT[C/G]TGGCCTCCTCTTAGT	10043
rs539550469	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35313638	TTAGGTCAGGCCAGA[C/T]TCGTCCCACTCCACC	10043
rs539553800	snp	C/G	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35326787	CTAGGAGGAGAGAGG[C/G]TGGGATCCCAGTCCT	10043
rs539561770	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35320028	AGCCAGGCAGACAGC[C/T]GGATGGGTCCCAGTG	10043
rs539652356	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35332140	GATTCTAAATCAGTG[G/T]AAAGTGGGGGGTACC	10043
rs539711044	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35309875	AAGCAAAACCTTCCC[A/C]AGGAGCCGCCCAAGA	10043
rs539741051	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35337207	TCCCAAAGTGCTGGG[A/T]TTTCAGCCACTGCAC	10043
rs539775939	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35315452	GACACTTGTTTGGCC[C/T]GCTCTGTTCTTCCCA	10043
rs539985088	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35338648	CTGTGCCCCCCAGCC[C/T]GCTCCGTTCTTGCAT	10043
rs540157095	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35309344	CCATCTCACCGATTC[A/C]CCCTTAGAACTGAAA	10043
rs540203575	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1	GRCh38.p7	22:35315160	GGAAGAAGCTGAGGC[A/G]GTAGTCTAGCGGGAG	10043
rs540211705	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35321468	CAGTGGCGTAATCTC[A/G]GCTCACTGCAACCTC	10043
rs540225389	snp	C/T	0.00358779	0.0422022	intron-variant	TOM1	GRCh38.p7	22:35328155	GTCTGTGTGCCTGAC[C/T]GAGCTGACTCTGCAG	10043
rs540270525	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35320787	ACTGTGTCCCCAGCA[C/T]CTAGCATGGTGCTAC	10043
rs540351530	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35326947	CCTCCCCGCCTTGTG[A/G]GGAGCCACCCTCCAG	10043
rs540357991	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35304376	TGAGAGGATTCCAGA[G/T]CCTTTGTACCAGCTG	10043
rs540401659	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35345918	ACACTTAAAGTCCCC[A/G]TCTCCTGCCACCTGC	10043
rs540402878	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35317090	GGGGGCTGGGGCAGG[A/G]GACAGAGATAGATTT	10043
rs540414582	snp	C/G			intron-variant	TOM1	GRCh38.p7	22:35305485	GCCAACATGGTGAAA[C/G]CCTGTCTCTACTAAA	10043
rs540464553	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35322504	CGTGGGCCTCCTAGC[C/G]GTCAGCATGGGTTTG	10043
rs540472581	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35345451	CCCGAAGGGTGTGTC[A/G]GAACTGGGGTTCTTC	10043
rs540704985	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35346639	CGTGCTGTGTGTTAT[C/T]CCATTTCAGCTTCCC	10043
rs540716687	snp	C/G	0.00119737	0.0244387	intron-variant	TOM1	GRCh38.p7	22:35339748	TCTCTACTAAAAATA[C/G]AAAAAATTAGCCGGG	10043
rs540721212	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35337181	GACCTCGTGATCCGC[A/G]CGCCTTGGCCTCCCA	10043
rs540735002	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35333692	CAGCCCCACAAGTCC[A/T]GAGCCGCCTTGGATC	10043
rs540784559	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35311537	AGGGGCAGTCAGCAT[C/T]GAACTGAGCACCTAG	10043
rs540835258	snp	A/G			intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35335049	TCAGGGGGTACTTTC[A/G]GCAGCATAGGCACGT	10043
rs540947201	in-del	-/CA	0.00597247	0.0543191	intron-variant	TOM1	GRCh38.p7	22:35342782	CACATCTACACCCAC[-/CA]CACACACCTCCACAC	10043
rs540986716	in-del	-/C	0.00358779	0.0422022	intron-variant	TOM1	GRCh38.p7	22:35343595	ATACACCTACACACA[-/C]CCCTACACACACCAC	10043
rs541018879	snp	C/T	0.00438332	0.0466095	utr-variant-5-prime, upstream-variant-2KB	TOM1	GRCh38.p7	22:35299366	AACCCCTTGCCCTTG[C/T]CTCTGATTTAAGGTA	10043
rs541029877	snp	A/G	0.000798403	0.0199641	downstream-variant-500B	TOM1	GRCh38.p7	22:35348071	GGGGGCCATCCGAGA[A/G]GTGAGCATCTGTAGA	10043
rs541074314	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1	GRCh38.p7	22:35312099	CTCTACTAAAAATAC[A/G]AAAAAAAATTAGGCG	10043
rs541080744	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35343141	ACACACACACATCTA[C/T]ACCCACCACACACAC	10043
rs541100955	in-del	-/T			upstream-variant-2KB	TOM1	GRCh38.p7	22:35297827	TTGTCTCTGTTTTTG[-/T]TTTTTTTTTGTTTTT	10043
rs541118762	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35302910	TCCCTGGCTGTGATT[A/G]CTGATGACACAGTAT	10043
rs541183937	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35322637	AGTGGAGAGTGGGGA[A/G]GGAAGTTCAGTGCCT	10043
rs541209182	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35330087	GATCGAGACCACCCT[A/G]GCTAATATGGCGAAA	10043
rs541216710	snp	C/T	0.00358779	0.0422022	intron-variant	TOM1	GRCh38.p7	22:35323443	TGAGTGCCAGGTGGG[C/T]AGGCTCACAGGTGAG	10043
rs541412288	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1	GRCh38.p7	22:35318794	GGAAGTGCTGCCAGA[C/T]GAGGCCTCCATCCTG	10043
rs541486288	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35331563	GGAGGAGCAGTTCCT[C/T]TAAAGAGTACTTAGG	10043
rs541499926	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35318342	TACTAGAGAGACTCC[A/G]GCTTTTCTGCGAGCA	10043
rs541539476	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35340917	AGGACGCTGGGGTGG[G/T]CCATCTGGGCCTCTC	10043
rs541575009	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35330758	TCACAGCTGAGAGCA[C/T]GGCCCTGCAACCAGA	10043
rs541589837	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	TOM1, MIR6069	GRCh38.p7	22:35336306	TTAAATGCTTCTGGT[A/G]GATCTTCCAGCTCTG	10043
rs541589994	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35343367	TCTACACCCACCACA[C/T]ACCTCCACACACACC	10043
rs541623345	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35314331	TTAGGCCACATATCC[C/T]CTCCCACCCCGCAGA	10043
rs541681326	snp	C/T	0.0023933	0.0345097	intron-variant	TOM1	GRCh38.p7	22:35313929	TGAAGGTTACAGCTC[C/T]GAGGTCGGGGAATCA	10043
rs541682668	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35342692	TGCCTCATCCCTCTA[C/T]ACCAGCCGCCACATC	10043
rs541692090	snp	C/G	0.000399281	0.0141238	downstream-variant-500B	TOM1	GRCh38.p7	22:35348456	CTCGATGTATAGATG[C/G]GGAGACTAGGACTCC	10043
rs541724771	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35313265	GGCAGGAGAATCGCT[A/T]AAACCCGGGAGGCAG	10043
rs541744792	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35319578	GGACGCTGTCCCTGC[A/G]CTCTAGGAGGCTTCT	10043
rs541758741	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35326222	AACTATAACTCAGCC[A/T]CATGATTTAGAATGT	10043
rs541777382	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35338209	CTCCCATGCTGCTGA[A/G]ACAAGGTGGGGGCAG	10043
rs541837237	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35331473	CTTGGATTGGCTGAG[C/G]TTCATTGTGCCTACC	10043
rs541868832	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35303086	GCTAATCAGGAATGA[A/G]TGTCAGTCACTGGAA	10043
rs541901757	snp	G/T	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35344533	TGGCAGCTAAGAGGC[G/T]ATGGGGATAGCGGAG	10043
rs541901919	snp	C/T	0.00159617	0.0282053	intron-variant	TOM1	GRCh38.p7	22:35344171	GGCGCTGCCGTCCCT[C/T]CGCCATCAGCGTGAC	10043
rs541930521	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35309387	AGTGGCTCACACCTG[C/T]AATCCCAGCACTTTG	10043
rs541975235	in-del	-/ACCTGGAGGA	0.00159617	0.0282053	intron-variant	TOM1	GRCh38.p7	22:35314162	GTTGTCCACACCTGG[-/ACCTGGAGGA]ACCTGGAGGAACCTA	10043
rs541981917	in-del	-/A			intron-variant	TOM1	GRCh38.p7	22:35307033	CTCTTCTGGTTTTAG[-/A]AAAAAAAAAACCCAA	10043
rs542045200	in-del	-/C	0.00119737	0.0244387	intron-variant	TOM1	GRCh38.p7	22:35305440	CCGAGGCGGGTGGAT[-/C]CACGAGGTCAAGAAA	10043
rs542048704	snp	C/G	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35327456	ACATGCATTCTTTCC[C/G]AATCCTCATGACAGT	10043
rs542134476	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35332924	AAGCTCTGCCTGGCC[A/G]TGTGTGGGGGCCTGT	10043
rs542160301	in-del	-/A	0.00438332	0.0466095	intron-variant	TOM1	GRCh38.p7	22:35339331	GCAAGACTCCATCTC[-/A]AAAAAAAAAGAAAGA	10043
rs542303009	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35321047	GCAGCTGGCCAGGAC[A/G]GGGCATCAGAACACT	10043
rs542426022	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35321078	ATGCTAGCTGGGCTC[A/G]GGGACTCATGCCTGT	10043
rs542437392	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35326980	CCTTGTTAGCTGCTG[G/T]GTTAGACCCAGGAGA	10043
rs542464461	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	TOM1	GRCh38.p7	22:35298295	ACATCCAGACTCGTG[A/G]GGGCAAAGGCATTTG	10043
rs542507521	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	TOM1	GRCh38.p7	22:35297487	TTGAGACGGAGTCTC[A/G]CTCTGTCTCCCAGGC	10043
rs542531709	snp	C/G	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35304429	TCAAGGATTTCAAAC[C/G]CTTTCCAGATATTCT	10043
rs542576138	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35345552	AGTCTCCTGGCTCTG[C/T]ACCTCCATCACCCAC	10043
rs542594073	snp	G/T			intron-variant	TOM1	GRCh38.p7	22:35313561	CAGGCAGTCTTATCC[G/T]GATTTTACGGGTGCA	10043
rs542598869	snp	A/G			upstream-variant-2KB	TOM1	GRCh38.p7	22:35299012	GAGATTCTTAGCTTG[A/G]GGTCCACGGTTGTAC	10043
rs542640314	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35322750	CCATGTTTAGCTCAG[A/G]GACAGCATTGGGATT	10043
rs542642933	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35316226	GCCCTGTGTCAGAAC[A/G]GGGTCTCACCCTTAA	10043
rs542685494	snp	G/T	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35328664	TGTTGAAAGGCACCC[G/T]CCCTGTCCCCGTGCT	10043
rs542704632	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35315895	CCCACCGAGTCCACC[A/G]TGGTATCCCAGTGCC	10043
rs542760224	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35321722	CACTTTTAACAAAAC[A/G]CTCTCATCTTTTCTC	10043
rs542798606	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35340390	AGTGAGGTGGAGGCC[G/T]CGGGGAAGTCTTGAG	10043
rs542817962	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35304951	TCAGTGGTTGGGGTG[G/T]TGGGAGCTGGGTGTG	10043
rs542872506	snp	A/T	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35317707	AGTGACGATGGGACA[A/T]TGTGTATAGAGCAGT	10043
rs542944803	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35303839	TACTAATATGCCACC[A/G]TCCCACTCTGTTAGT	10043
rs543069124	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	TOM1	GRCh38.p7	22:35348081	CGAGAGGTGAGCATC[C/T]GTAGATGGTGCAGGC	10043
rs543074106	snp	A/G	0.00481496	0.0488292	intron-variant	TOM1	GRCh38.p7	22:35317839	GTTTACCCATTCAGG[A/G]CCCCCTCATGACTTT	10043
rs543104514	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35313308	GCCAAGATCGTGCCA[C/T]TGTACTCCAACCTGG	10043
rs543125730	snp	A/C	8.27164e-05	0.0064305	intron-variant	TOM1	GRCh38.p7	22:35300000	GTCCCTGGAGCCCCC[A/C]ACAGCTCCGCCCCGG	10043
rs543148126	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35312717	TGTGAACTGGATGAG[C/G]CTGACTGAATGAGGA	10043
rs543153148	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	TOM1	GRCh38.p7	22:35299089	GCTGCCTTTTTTCTT[C/T]AGAAAGGCTCATGGC	10043
rs543161341	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334565	CCCTGCTTAGTAAGC[A/G]CGCCCTTAGTATCCC	10043
rs543244407	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35330543	TCCCTTCCCTTCCTC[C/G]CTGTTCTCCTGGTCT	10043
rs543282473	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35324004	AATTTACCATCCACG[A/G]AGCCTCCACTTCTTC	10043
rs543327991	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	TOM1, MIR3909	GRCh38.p7	22:35336012	GATGCTGAGAGGGTG[A/G]TGGGGCCCACTGGGC	10043
rs543365795	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35304758	GCTGGGATTACAGGC[A/G]TGAGCCACTGCACCC	10043
rs543417023	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1	GRCh38.p7	22:35300297	TTTTCGTGGTTAAAG[A/G]GACTGCGTGGTTGGC	10043
rs543445635	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35341691	CACACAGCAATTCAG[G/T]CGTGACTAAAACTAG	10043
rs543481830	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1	GRCh38.p7	22:35347823	GAGGCTTCAGGGGAT[A/G]CTGGGGCCCCACTGC	10043
rs543510609	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35319281	AGGCTCGGCGTCGGT[C/T]AGGTGCATTGCTATT	10043
rs543596111	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35324778	TAGTCTCGAACTCCT[C/G]AGCTCAAGTGATCTA	10043
rs543762079	in-del	-/TACACA	0.00159617	0.0282053	intron-variant	TOM1	GRCh38.p7	22:35343762	ACACACCCCTACACC[-/TACACA]TACACACCTACACAC	10043
rs543776032	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35330271	TGGGCGACAGAGCTC[C/T]GTCTCACAAAAAAAA	10043
rs543835173	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35313826	GCCATAAACAACTGC[A/T]AAGCCGCCTGATGAC	10043
rs543889421	snp	C/T	0.00279162	0.0372561	intron-variant	TOM1	GRCh38.p7	22:35342713	CCGCCACATCCACCA[C/T]ACACACCTCCACACA	10043
rs543895726	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35313353	CTGTCTCAAAAAAAA[A/G]AAAGAAAGAAAGGGG	10043
rs543916790	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35318871	TCATCCAGCTCTCCC[A/G]CGGCCAGTGCAGGGT	10043
rs544076712	snp	A/C	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35343439	CACACATATCTACAC[A/C]CACCACACACACCTA	10043
rs544119472	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35314424	TTGCCTGCACTGCTT[A/G]GGTCACATCAGACTC	10043
rs544138638	snp	C/G			upstream-variant-2KB	TOM1	GRCh38.p7	22:35298592	GCGTGTACCACCACA[C/G]CTGGCTAATTTTTGT	10043
rs544156300	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35333672	CTCGGGGTCACTGCC[C/G]CTGGCAGCCCCACAA	10043
rs544159650	snp	A/G	0.00159617	0.0282053	intron-variant	TOM1	GRCh38.p7	22:35307972	TAAATCACCAGACCC[A/G]CGTAAAGCGTATTGC	10043
rs544177161	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35320269	GGCTTCACCTCATGG[A/G]TGTGGAGGTCAGGAG	10043
rs544333978	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1	GRCh38.p7	22:35310098	GACAGGTAAATGTGG[C/T]GTGTGGGTTCCCACA	10043
rs544343855	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35332278	TCTGGTAGCAGCTGG[C/T]ACCCTCAGATATCCA	10043
rs544363407	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35345234	CTATCATGAAATCTG[C/T]GTCTGCAGAGACACC	10043
rs544364391	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35344699	AAACTGGCCTGGTTG[A/G]GGAAAGACTCTGTCT	10043
rs544524396	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35327509	CTTGGTCACAGTTGG[C/G]GACATGTTACCACCA	10043
rs544562698	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35324868	AAGGTTTGAGGCTTA[A/G]TATGAGATTCTAGGG	10043
rs544592425	snp	C/T	4.98227e-05	0.00499088	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35323054	CTGTGTCAAGAACTG[C/T]GGGCACCGCTTCCAC	10043
rs544616578	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35346002	GGCTGCTTCCCAGAG[C/T]CTGCTCCCAAGGTGA	10043
rs544674859	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35338281	ACCTCACCCAGCAGT[A/T]TATAGATGTGTTTTC	10043
rs544833572	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35321580	ATTTTTGTATTTTTA[A/G]TAGAGACAGGGTTTC	10043
rs545005523	snp	A/G			downstream-variant-500B	TOM1	GRCh38.p7	22:35348402	GCTACGCACTGGCTC[A/G]TAGCATCACAACAGC	10043
rs545013097	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35311430	CAGCTCCACGATGTC[C/T]CAAAACAGCCAGACT	10043
rs545044182	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35316903	CATGAATCATCACCT[C/G]TCTTTGGGGTAGTTC	10043
rs545079474	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35311090	GCACAGAAGCCTGAG[A/G]AGGGTGATGGGGTGG	10043
rs545181950	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35328686	CCCCGTGCTAAGGGC[A/G]ATGAGGAAATCCCGG	10043
rs545187605	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35306652	CCTATCAGATAGGGC[C/T]GTCGTGTTGTTGTGC	10043
rs545232014	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35340983	CAAGAGAATCCAGTA[C/G]CTCCCATGTGTGGTG	10043
rs545245749	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35341744	CACTACCTTGCAGCC[C/T]GCCCACAGGGAGGAA	10043
rs545289719	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35320005	TCCTGGATGGGGTCA[A/G]CACTGACAGCCAGGC	10043
rs545345130	snp	A/G	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35335334	TCCAGAGAGCCCAGG[A/G]ATAACCTCTCCACAC	10043
rs545355892	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35305170	GCGATGTTGAGGAGA[C/T]ACCAGGCTGGGAGGC	10043
rs545393868	snp	A/G	0.00159617	0.0282053	intron-variant	TOM1	GRCh38.p7	22:35312176	TTAAACCCAGGAGAC[A/G]GAAGTTGCAGTGAGC	10043
rs545438992	snp	A/C			intron-variant	TOM1	GRCh38.p7	22:35324622	GGCACCATCTAGGCT[A/C]ACTGCAACCTCTCTC	10043
rs545452132	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35323350	AGGCTTGCCAACTGC[A/G]TGCTTTGCTGTGGAG	10043
rs545567667	snp	A/C/G	0.000798403	0.0199641	intron-variant, nc-transcript-variant	TOM1, MIR3909	GRCh38.p7	22:35335668	GCTGTCCTTCCTCTG[A/C/G]GGAGCAGGCTCCGGG	10043
rs545625728	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1	GRCh38.p7	22:35347886	GTTCCTTCTGGCCGG[G/T]CACCACAGCACTGGG	10043
rs545627421	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35325513	AGGATTGGAGACAAG[C/T]TCTGTTTAGAAATAA	10043
rs545638842	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35312761	CAGAAGCTCAGAGGC[A/G]TGAGAGGGCAAGCCA	10043
rs545678215	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35341762	CCACAGGGAGGAAAC[A/G]CACCACACAACTCCA	10043
rs545701981	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35318237	GAAGCCCAGCCTTGT[A/G]TGCAGCATCTGCCTA	10043
rs545764539	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35344104	AAGTGGCAGCAGGCC[C/T]CCTGACCCGAAAGGC	10043
rs545802008	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35331254	GCATGCACCACCACA[C/T]CCAGCTAATTTTCTT	10043
rs545802979	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35343569	CACCTACACACACCA[C/T]ACCTACACTCATACA	10043
rs545832717	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	TOM1, MIR3909	GRCh38.p7	22:35336184	GTTCTCCTGCAGGCC[C/T]TCCCCAGGGCTTGGT	10043
rs545871430	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1	GRCh38.p7	22:35342659	TGTGGCTCACCCCCC[A/G]GTGGGTACCACAATA	10043
rs545931266	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35314305	CCTCCTCTTCCTCTC[C/G]CCTTTCTCGTTTAGG	10043
rs546018910	in-del	-/T	0.00517822	0.0506191	intron-variant	TOM1	GRCh38.p7	22:35346556	AGGACCACCCACCCC[-/T]TGTGACCCTCCAAGG	10043
rs546034684	snp	A/G	0.00199481	0.0315187	intron-variant	TOM1	GRCh38.p7	22:35305592	TTGAACCTGGGAGGC[A/G]AAGGTTGCAGTGAGC	10043
rs546130178	snp	A/G	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35338109	GCCCATCAGCCTTGC[A/G]TGCCCTCCCAGTTCC	10043
rs546212885	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35301978	TAAAAGACCTGGCTT[C/T]AAAGTCAGCCACATA	10043
rs546256436	snp	A/G	0	0	intron-variant	TOM1	GRCh38.p7	22:35308977	GATGGAACTTTCCAC[A/G]CTGGGTCTGGAAAGA	10043
rs546259745	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35331836	GAGGTTGCAATGAGC[C/T]GAGATCGCACCACTG	10043
rs546274518	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35308080	GGGAACTTGGCCAGC[A/T]GGCTCCCCTTGTCCT	10043
rs546295723	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35313869	GCAGGGCCCGGTTCT[C/G]TCAGGAGCTGGAAGA	10043
rs546380719	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35326561	CTATCCTTAGATGAG[C/T]CTGGGACACCAAAAT	10043
rs546426543	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35332362	CCATGTCCTAATTTG[G/T]GCTTCAGCACTTCAG	10043
rs546428214	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35333293	CCAGTCCTAGCTCCT[A/G]GGGCCCTGGTGACAG	10043
rs546494305	in-del	-/AT	0.00557542	0.0525036	intron-variant	TOM1	GRCh38.p7	22:35343511	CACACCTACACACTC[-/AT]ACACCTACACACACC	10043
rs546504611	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35302697	CCATCCCCTTCATTT[C/T]ACACTGGCGGAGACT	10043
rs546518066	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35338428	GGCACTGGAGCTATT[G/T]ATCAGTCTCCTGAGT	10043
rs546548267	snp	A/G			intron-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35337262	GAAGGGAAATCATGG[A/G]TTTCTGCGTGTTCTG	10043
rs546550167	snp	A/G	0.00358779	0.0422022	intron-variant	TOM1	GRCh38.p7	22:35302471	CTCCCAAGGTAGCCG[A/G]GATTACAGGCACGCT	10043
rs546576470	snp	A/G	0.000272035	0.0116595	intron-variant	TOM1	GRCh38.p7	22:35321695	TGAGCCACCGCGCCC[A/G]GCCAGGTTCTGCACT	10043
rs546703053	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35327207	GGTACTGGGTTCTGT[C/T]GCTGTGAGTAACATG	10043
rs546705801	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35321116	ACATATTGGGAGGCC[A/G]AGGTGGGAGAATCAT	10043
rs546745873	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35322924	AGTCCCATCTCCTCT[C/T]CCGGGCCTCCTCTCT	10043
rs546753705	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35346091	GAGGAAGCATAACAG[C/T]GCCAGGCTCTTACCT	10043
rs546894901	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1	GRCh38.p7	22:35344805	TATTGGTTTCTTGAG[C/T]ATCTCCTCCATGCCA	10043
rs546959050	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35315453	ACACTTGTTTGGCCC[A/G]CTCTGTTCTTCCCAG	10043
rs547030833	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35328306	ACGCCCCAAGCCAAG[A/G]CCATGAGATGTGAGC	10043
rs547060393	in-del	-/T	0.080339	0.183617	intron-variant	TOM1	GRCh38.p7	22:35331273	GCTAATTTTCTTTTC[-/T]TTTTTTTTTTTTCTT	10043
rs547117053	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334233	ACGTGCCACTTCCCC[A/G]GCACCAAGCCCTGGG	10043
rs547193592	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35304083	TGCGGTTTTGCTATT[C/T]TTTTCCCATTTCACC	10043
rs547260156	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35329778	ACCTTTATTCTGGAA[C/T]CTGCACGAAGCCAAG	10043
rs547320576	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334711	TACATAGTCTGATCA[A/G]AGGGGGAAACTGAGG	10043
rs547480559	snp	A/G	0.00438332	0.0466095	intron-variant	TOM1	GRCh38.p7	22:35308647	CTGACCATCCAGATT[A/G]TCAGCAATACCTTTT	10043
rs547530409	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35304542	GGAGTGCAGTGGCGC[A/G]ATCTCGGCTCACTGC	10043
rs547534576	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35305472	TGAGACCATCCTGGC[A/C]AACATGGTGAAACCC	10043
rs547539810	snp	A/C/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35332146	AAATCAGTGGAAAGT[A/C/G]GGGGGTACCCTGCAG	10043
rs547606292	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1	GRCh38.p7	22:35311983	AGTTCGGCTGGGCAC[A/G]GTGGCTCACGCCTGT	10043
rs547638829	snp	C/G/T	0.000104746	0.00723623	intron-variant	TOM1	GRCh38.p7	22:35322995	CTCCTCTCCTCTGAC[C/G/T]AAGGTGCTCGACGGC	10043
rs547716813	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35329784	ATTCTGGAATCTGCA[C/T]GAAGCCAAGTTAAAC	10043
rs547769053	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35313101	CCTGTAATCCCAGCA[A/C]TTTGGGAGGCCAAGG	10043
rs547769231	snp	G/T	0.00199481	0.0315187	intron-variant	TOM1	GRCh38.p7	22:35306057	TAAATGAATGAGAAT[G/T]ACTGTGCATAAATAA	10043
rs547781610	snp	A/G	0.00358779	0.0422022	intron-variant	TOM1	GRCh38.p7	22:35341302	TATTACGGCACTTAC[A/G]CTTCGCAGTACCGCC	10043
rs547828925	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35318646	TAGGTCTTTGTCCTC[A/G]AAGGTGCTCTGTTAG	10043
rs547831801	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1	GRCh38.p7	22:35312333	CACTGTCTCAGCACC[C/T]GGTCTTTCCTGCCAT	10043
rs547886096	snp	A/G	0.00199481	0.0315187	upstream-variant-2KB	TOM1	GRCh38.p7	22:35298378	TACAGTAAAGACATC[A/G]GACCCCATGGCTGCT	10043
rs547901228	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35346837	GGACCCAGTGCTGAG[C/G]TTCAGCGGGGCCCGA	10043
rs547904470	snp	G/T	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35325005	GAGCTGCTTGTGGAG[G/T]GCCATGGCTGCTGTA	10043
rs547905351	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35308711	TCTGTACCTCAGCCA[A/G]CCACTTCAAGCCTCT	10043
rs547923097	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35330260	GCACTCCAGCCTGGG[C/T]GACAGAGCTCCGTCT	10043
rs547948936	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35343675	CTACACACACCCTTA[C/T]ACACACCACACCTAC	10043
rs547980190	in-del	-/T	0.00119737	0.0244387	intron-variant	TOM1	GRCh38.p7	22:35328950	CCCATATGGCTATGG[-/T]TTTTTTATTTTTTTA	10043
rs547986917	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35342943	TACCTCCACTCATAC[A/G]CCTACACACACCCCT	10043
rs548082349	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35308141	TCCAGCCTGCCAGCT[C/T]ACCCTACAGATTTTC	10043
rs548090865	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35341809	GCTGATAAACCGGTT[A/G]TCACTGATTTATCTC	10043
rs548120691	snp	A/G	0.00398564	0.0444627	downstream-variant-500B	TOM1	GRCh38.p7	22:35348159	CTCCCACCTCACATG[A/G]CAGGCTCCAGCCACC	10043
rs548141988	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35302878	TCTTTTAGATAAAGA[A/G]GCGGAGGAAGTACTG	10043
rs548228782	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35304844	GCTGTCAGCTTACCC[C/G]TAAGCACTTGGAGTC	10043
rs548242307	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35332474	ACAAGGCCACGACTT[A/G]AACAGACCCCACACT	10043
rs548257583	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35337148	TCACCATGTTAGCCA[A/G]CATGGTCTCGATCTC	10043
rs548282262	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35324142	CCAAGCTCACGTCTG[A/T]CTGACTCCTGGCAGG	10043
rs548377099	in-del	-/CA			intron-variant	TOM1	GRCh38.p7	22:35343527	TACACCTACACACAC[-/CA]CACACACATCTACAC	10043
rs548765245	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35309576	TTGAACCGGTGAGGC[A/G]GAAGTTGCAGTGAGC	10043
rs548782460	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35314598	GATGTTCCCTCCTCC[A/G]GGAGATGAGAGGTGC	10043
rs548859575	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35327671	TTGATGTGAGTTAAA[C/T]AAGGTATTGCATGAA	10043
rs548893158	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35314487	TCCCACCTGATTGCC[A/G]GGTATGGGATTTCTC	10043
rs548950261	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35310626	TAGCTAGTAAGGGAT[C/G]AATGAGTGCCCAAGT	10043
rs548966135	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35338594	AATGAGACCCTTTTT[A/G]CCATTTCCAGGCAGG	10043
rs548996612	snp	A/G	0.00358779	0.0422022	intron-variant	TOM1	GRCh38.p7	22:35342293	ACATGCCTGCTGTGT[A/G]CCCTGTGCCATGTGC	10043
rs549009743	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35316016	CCCTTGCAGGACAGC[A/G]TGACATCACGTGGAA	10043
rs549020147	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35302896	GGAGGAAGTACTGCT[A/C]CCTGGCTGTGATTAC	10043
rs549134607	snp	C/T	0.000547895	0.0165423	intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334303	TTGTGGATGGGTCTT[C/T]CACGTGGCCTTTCTG	10043
rs549277030	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35339068	GGGCGTGGTGGCTCA[C/T]ACCTGTAATCCCAGC	10043
rs549278938	snp	C/G/T	3.37469e-05	0.00410762	intron-variant	TOM1	GRCh38.p7	22:35333371	CGAAGCTGCAGACAG[C/G/T]GGGGATGATCAGGGC	10043
rs549310488	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB	TOM1	GRCh38.p7	22:35298550	GCAATTCTCATGCCT[C/T]AGCCTCCCAAGTAGC	10043
rs549322223	snp	A/T	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35329426	TTTTACCAGTTTTAA[A/T]GTTTAATGGTAGTTT	10043
rs549406920	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35346177	TACAGATCAGAAGAC[C/T]GATAAGCAGCTGTCC	10043
rs549407804	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35335086	AGTGTGTCCACCAGG[G/T]TCTGACCCCTTGCCG	10043
rs549448666	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334786	ATTTGGCAGCACTAG[A/G]TTAGGAGCCTAGGGC	10043
rs549526016	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35340709	CTGAGATTGCACTAC[A/G]ACACTCCAGCCTGGG	10043
rs549564518	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35346755	CAAGGAAGGTCCTAC[A/G]GCTCAGGGAGGAGCC	10043
rs549585413	snp	A/C			intron-variant	TOM1	GRCh38.p7	22:35341240	GAAGAGCTTAAGTGA[A/C]ACCACAGGTGTACTG	10043
rs549595195	snp	C/G			intron-variant	TOM1	GRCh38.p7	22:35307799	ATTTAGGGACAGACA[C/G]AGGGGTCTACTGTTT	10043
rs549644957	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35332448	ATTTACCCGAGGTCA[C/T]GTGATAAGTGACAAG	10043
rs549692508	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35318475	ACTGGCGTTTGCCGG[G/T]CGTTTCTGGTGTTGG	10043
rs549878713	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35342801	CACACCTCCACACAC[A/G]CCTACACTCATACAC	10043
rs549885408	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1	GRCh38.p7	22:35299502	CACCCAGGGTAGGTG[A/T]GCAGTCACAGTGAGG	10043
rs549934302	snp	C/G			intron-variant	TOM1	GRCh38.p7	22:35323971	GGGCCACACACGTCA[C/G]GGAGGGCCCCCTGTC	10043
rs549964483	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1	GRCh38.p7	22:35314445	CATCAGACTCATGCA[C/T]GGGGTGGGGGCGGGG	10043
rs549967353	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35312359	GCCATGGAAACGACC[C/T]TTTGGAATTGTCAGT	10043
rs550001425	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35341454	GAAAAGCCCTAAGGT[A/G]CAAAGGAGAGTGAGT	10043
rs550044273	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1	GRCh38.p7	22:35347383	GTGTGGAGGCAGTGG[A/G]ATGAACTGGGGGACA	10043
rs550105628	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35317479	AGGCGTGAGCCACCG[C/T]GCCCAGCTCAAAAGA	10043
rs550113510	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35312654	TGACTGAGGGTGTGA[C/T]GTGCTTATTAGTCCC	10043
rs550141508	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35313979	CTGGCAACCACTGTC[C/T]GTGTTTTTATTCCCC	10043
rs550156418	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35342047	TTGGGAGGCTGAAGC[A/G]GGAGGATCACTTAAA	10043
rs550168885	snp	C/G	0.0023933	0.0345097	intron-variant, downstream-variant-500B	TOM1, MIR3909	GRCh38.p7	22:35335794	GCTGTCCTGGAGGGG[C/G]CACCAGGCTCTGTGG	10043
rs550204689	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35313603	TCAGAGGGGCTGGAT[C/T]TTTGCCCACATTCTA	10043
rs550257238	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35306958	TATGGATAGAACTGG[A/T]GAATAGGTTTTATTC	10043
rs550317761	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35312892	AGAGGAAGTTGTGCT[G/T]GGAGTTATGTTTGAG	10043
rs550348891	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35319705	GGAAAGAAGTCACTA[C/T]AAAGCGCTGAAGTAG	10043
rs550419486	snp	C/T	0.00159617	0.0282053	intron-variant	TOM1	GRCh38.p7	22:35308800	GACATTTCCTTTTGT[C/T]AGGTACTATAGTTAG	10043
rs550477432	snp	A/G	0.00199481	0.0315187	intron-variant	TOM1	GRCh38.p7	22:35308189	CACCTGCATAAGCCA[A/G]TTCCTTAAGCGCTCG	10043
rs550480088	snp	C/T	5.15495e-05	0.00507662	intron-variant	TOM1	GRCh38.p7	22:35330317	CTCTGAGTCATGTGA[C/T]TGTGGTTGCCTCACT	10043
rs550480240	snp	C/T	0.00318978	0.0398085	intron-variant, downstream-variant-500B	TOM1, MIR6069	GRCh38.p7	22:35336362	GCTTGGTGTCCAGCC[C/T]GCTCCTCCCTGTACC	10043
rs550508380	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35344216	ATGGGAGGCGGCTGC[A/G]GGAAAAGCCTCAGTG	10043
rs550519981	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35327050	TGTGGAGATGGTAAC[A/G]GTTGGTAGCGCCTCT	10043
rs550534992	in-del	-/AC	0.496034	0.0443518	intron-variant	TOM1	GRCh38.p7	22:35343294	TACACACACAGCCCT[-/AC]ACACACCACACCTAC	10043
rs550607883	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35333133	TTATCCAGGCCCATA[A/G]AGAAATCCCCTTCTA	10043
rs550608036	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35326755	TAGGAGGAGAGAGAC[A/G]GCGGGATCCCAGTCC	10043
rs550619742	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35320586	CCCAAACTGCTCTGC[C/T]CCCACTCCCCCCAGG	10043
rs550655968	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35319122	GGAGTGGTGGGCAGA[A/G]GTCAGAAGAAAGAAA	10043
rs550695404	snp	A/G/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35344294	CCCGGAAAGCTGGGG[A/G/T]TGCTCGCAGGGCTCC	10043
rs550731935	snp	G/T			intron-variant	TOM1	GRCh38.p7	22:35346589	AGGAACCAGCACTCA[G/T]CAAGGTCCCACTGGG	10043
rs550785843	snp	A/T			intron-variant	TOM1	GRCh38.p7	22:35329272	TTTTTTTTATTTTTC[A/T]TAAGTTTAAATATGA	10043
rs550898559	snp	A/T			intron-variant	TOM1	GRCh38.p7	22:35326606	ACAAAATCCCAGTCC[A/T]CTAGGAGGAGAAAGA	10043
rs550917997	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35320479	CTTCAGCCCTCCCCG[A/G]CCTCCCCCACACTCA	10043
rs550995842	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35321173	TGGGCAACATAGCAA[A/G]ACCCCATCTCTATTT	10043
rs551102226	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35339134	TCAGGAGTTCAAGAC[A/C]AGCCTGGCCAACATG	10043
rs551186214	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35345672	GTGCTGAGCTGGCAC[A/G]TCTTCCACCTTGTCA	10043
rs551331483	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35339928	AAAAAGAGCGGACCC[C/T]AAAGCAGCGGGGAGA	10043
rs551367678	snp	A/G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35333773	GCTTCAATCATCTGC[A/G/T]TGAGCTTGGGCAAGT	10043
rs551490872	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35344977	GGGGTGAGCTAGGTC[C/T]AGCTCTTTCTCACTC	10043
rs551518354	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35303537	TGAGACAGAGTCTCA[A/G]AAAAGGCTGGAATGC	10043
rs551590628	snp	G/T	0.00318978	0.0398085	intron-variant	TOM1	GRCh38.p7	22:35307664	CCTCGCTCCTGCTGG[G/T]GAAGGTAGAGAAGGG	10043
rs551638386	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334213	TCGCGCATTCCCCCA[C/G]CCACACGTGCCACTT	10043
rs551687320	snp	A/G	0.00478085	0.0486577	intron-variant	TOM1	GRCh38.p7	22:35327827	CCAGCCTTGAGATGC[A/G]CCAGCCACTGATCTT	10043
rs551716747	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35324063	TTCTTCCTGTTTGAG[C/T]GATGAGACTCAGAGA	10043
rs551738424	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	TOM1	GRCh38.p7	22:35299568	GGCTTCTGTGTAACT[C/T]ACCCAAGTCACTTCC	10043
rs551783539	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35340773	GAAAGCAGGGAGGGA[C/T]GAGTTGTGGAAACCG	10043
rs551802778	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35330182	CCAGCTACTTGGGAG[A/G]CTGAGGCAGGAGAAT	10043
rs551850939	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35318100	CAACCCGCTTGGCTG[A/C]AGAGGCCATCTGAGC	10043
rs551908919	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35322857	CCAGTAAACAAGTCC[C/T]CCAGTCCTGGCATTG	10043
rs551916982	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35342234	GTCGTGTGACGAGGT[C/G]GTATTGCATGCTGTG	10043
rs551961261	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35341260	CAGGTGTACTGTCCT[C/T]GGTATGGTGCCTGGC	10043
rs552037151	snp	A/G			upstream-variant-2KB	TOM1	GRCh38.p7	22:35298122	TGAAGAAAGACATGG[A/G]AAGTGCCTTGACCTG	10043
rs552063037	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35313455	TTCTCTTGGCCCAAG[A/T]CATAGTCATTGTAGC	10043
rs552195257	in-del	-/T	0.00159617	0.0282053	intron-variant	TOM1	GRCh38.p7	22:35308170	TCAACTTGCTAAGCC[-/T]TCACACCTGCATAAG	10043
rs552232006	in-del	-/TTT	0.00159617	0.0282053	intron-variant	TOM1	GRCh38.p7	22:35321574	CGGCAAATTTTTGTA[-/TTT]TTAGTAGAGACAGGG	10043
rs552376468	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35307088	TGAGGCCATCACCCC[A/G]TGAGAAGCAGGGGGA	10043
rs552389217	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35313068	ATACTGGCCGGACAC[A/C]GTGGGCAGTGGCTCA	10043
rs552504251	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35326495	GCCCACATCCCTTGG[A/G]ACAAGTGCTAAATCT	10043
rs552561602	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35332853	CCAGGGCACACCAGA[C/T]GTGTCATCACCCTGA	10043
rs552571366	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35346600	CTCATCAAGGTCCCA[A/C]TGGGCACCAGGTGCT	10043
rs552580694	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35331655	TTGGGAGGCTGAGCC[A/G]GGAGGATCACTTGAG	10043
rs552591067	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35301627	ATTCTTAGTGTCTTG[C/T]GAAACCTCACGAAAG	10043
rs552641126	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35307791	GACAGAGAATTTAGG[A/G]ACAGACAGAGGGGTC	10043
rs552657592	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35337259	AGTGAAGGGAAATCA[C/T]GGGTTTCTGCGTGTT	10043
rs552680901	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35327903	CACATGGTATTCCCA[C/T]GGCCCCAGCCCAGAT	10043
rs552701942	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35326817	TCTAGGAGGAGAGAG[A/G]GGGGGGGATCCCAGT	10043
rs552717608	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35300737	CCCTGGTGACAGGAT[A/G]CTCACAGTTCTGTGA	10043
rs552722575	snp	G/T	0.00119737	0.0244387	intron-variant	TOM1	GRCh38.p7	22:35320035	CAGACAGCCGGATGG[G/T]TCCCAGTGGCCACTG	10043
rs552795949	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35306353	GGTGCTTATCCCCAC[A/C]GTGTGCCCATGTGAG	10043
rs552862660	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35335155	AGGAACAGTCTGCTT[A/G]ATGTTTTCTTCAGCC	10043
rs552897834	snp	A/G	0.000200582	0.0100125	intron-variant	TOM1	GRCh38.p7	22:35331350	CTCTTGGCCTCAAGC[A/G]GTCCTCCCTCCTTGG	10043
rs552926745	in-del	-/GGTGACG	0.00478085	0.0486577	intron-variant	TOM1	GRCh38.p7	22:35312630	TGTCTTAAAGGTTGT[-/GGTGACG]GGTGACTGAGGGTGT	10043
rs552953589	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35302413	CCATCTTGGCTCACT[A/G]CAACTTCCGCCTCCC	10043
rs553061865	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35320507	TCAGTGTGGCCTCCT[C/T]TTAGTTCCTCCAAGG	10043
rs553091733	snp	C/T	0.00199481	0.0315187	intron-variant	TOM1	GRCh38.p7	22:35343280	CTCCACTCATACACC[C/T]ACACACACAGCCCTA	10043
rs553097333	snp	G/T	1.91893e-05	0.00309746	intron-variant	TOM1	GRCh38.p7	22:35327425	TGGGGCTCAGATGAC[G/T]CCTGCCCAGCTGCCC	10043
rs553141995	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35314773	CCTGCTGAGAGATGC[A/G]GATGGCACAGAAGCC	10043
rs553200673	in-del	-/TTG/TTTG			upstream-variant-2KB	TOM1	GRCh38.p7	22:35297839	TTGTTTTTTTTTGTT[-/TTG/TTTG]TTTTTTTTTTTTTTT	10043
rs553245710	snp	A/G	0.00358779	0.0422022	intron-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35338154	GCCTAGCTGGCTGGC[A/G]CCCCCCAGAGGACAT	10043
rs553300514	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35324390	TTTGAGACCAGGCTG[A/G]GCAACATAGAGAGAC	10043
rs553441637	snp	A/G/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35314319	CCCCTTTCTCGTTTA[A/G/T]GCCACATATCCCCTC	10043
rs553659914	snp	A/G			intron-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35338087	GGGTCAGCCTCTGCC[A/G]CTCCCAGCCCATCAG	10043
rs553672936	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35304390	ATCCTTTGTACCAGC[G/T]GGTGTTGTCACAGCC	10043
rs553732419	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35310796	TTTGTGAGCTATAAC[C/T]GCCACCCTTAAAGAG	10043
rs553774835	snp	A/G	1.64822e-05	0.00287068	missense, nc-transcript-variant, intron-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35322017	AATAAGAACTTCCAC[A/G]AGGTGATGCTGGCTC	10043
rs553807116	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35333892	GGTTGCACTCTGGCT[A/G]AGTAGTTGGCCATTG	10043
rs553848806	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35328563	GCTCCAAGTGCTGCT[C/T]TTCTGCTCTTGAGAG	10043
rs553901997	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35323689	ACTCATCCCCAGAGA[C/T]ATCACCAGGCTGGCC	10043
rs553918374	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35317644	AGTCATGGTTTCCTC[A/G]TCCATTGAAGAGCAG	10043
rs553920643	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35311326	CAGGTAACAGGAAAC[G/T]CAACCAGCAGAGTCT	10043
rs553975189	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35305532	GGACGTGGTGGCACA[C/T]GCCTGTAGTCCCAGC	10043
rs554012103	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35306847	GGCAAATGAGCGGTC[A/G]CTGGCTGGGTGGCCA	10043
rs554025992	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1	GRCh38.p7	22:35345951	ACCTTGTGTTTGGCA[C/T]GCCCCCCAGAGAAGT	10043
rs554029453	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35324239	AGAGGTGTCCTGTAC[A/G]CAGCCCCTTCAGGCC	10043
rs554056714	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35316630	TGCAGCCGACTCCCG[G/T]CCTGGAAATCTTACC	10043
rs554119579	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1	GRCh38.p7	22:35316140	AGGTGTGCCAAGGCC[A/G]GCAGGGTGGCTGCAG	10043
rs554253481	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35318196	CCCGCCTCTCTTAGT[A/G]GCAGCCCAGATTCCA	10043
rs554354096	snp	A/G			intron-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35337183	CCTCGTGATCCGCGC[A/G]CCTTGGCCTCCCAAA	10043
rs554375870	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35312114	AAAAAAAAATTAGGC[A/G]GGCGCCTGTAATCCC	10043
rs554425541	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35328920	AGAAATAATTGACCA[A/G]TCTTAAAAATGAAAA	10043
rs554433658	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35342390	TCTCGTCTCCCTCCA[C/T]TCTGGGGCCCTAGGA	10043
rs554439382	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35335417	CTGTTAGCTGTATCT[A/T]TCTTTAGTCTGGGCA	10043
rs554571026	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1	GRCh38.p7	22:35347745	AGGAGCTGCGGCGGC[C/T]CAGGTACGAAGCTGC	10043
rs554592119	snp	C/T	0.00398564	0.0444627	intron-variant	TOM1	GRCh38.p7	22:35307236	CTTCATTATTATTTT[C/T]GTAGGGTTTTCTTTT	10043
rs554595314	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35312690	TGGTGCATGCTGAGT[A/G]CCAGATGAGCATGTG	10043
rs554613621	in-del	-/T	0.00159617	0.0282053	intron-variant	TOM1	GRCh38.p7	22:35308594	GCCTAGTTCCTTTTC[-/T]CTAGAGATCCCTGAC	10043
rs554715100	snp	A/C/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35317470	TGGGATTACAGGCGT[A/C/G]AGCCACCGCGCCCAG	10043
rs554778428	snp	A/T	0.0023933	0.0345097	intron-variant	TOM1	GRCh38.p7	22:35330130	TAAAACTACAAAAAA[A/T]AAAATTAGCCAGGCG	10043
rs554845489	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35308429	GCTGGGACTACAGGC[A/G]CGTGCCACCACACCT	10043
rs554866275	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35300780	GGGCCGAGGTTTCCT[C/T]ACCTGTAGTTGGCGG	10043
rs554922301	snp	G/T	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35300287	AGGGAGAAAGTTTTC[G/T]TGGTTAAAGGGACTG	10043
rs554942619	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35309808	GTGCTTGCATTCTCA[C/T]GGTAGGAAGCACAGG	10043
rs554944617	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35339670	AGCACTTTGGGAGGC[C/T]GAGGCGGGCGGATCA	10043
rs555027417	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35324714	CCACCATGCCCAGCT[A/C]ATTTTTTGTATTTTT	10043
rs555034390	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35318803	GCCAGACGAGGCCTC[C/T]ATCCTGAGAAATCAG	10043
rs555110569	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35314822	GCGTCAGCGGCTGCC[C/T]CGCCCTTACCTCTGT	10043
rs555127886	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35301712	CGAGGTTTTGTAATC[A/G]ATGCTCTCCAAGGGG	10043
rs555191144	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35307895	GCCAGGGGAGAAAGA[G/T]AGTTGGTCAAACATT	10043
rs555204913	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35344024	CTACACACACACCTA[C/T]ACTCATACACCTACA	10043
rs555248787	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35314157	ATCCTGTTGTCCACA[C/T]CTGGACCTGGAGGAA	10043
rs555308274	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35313793	GGTGCCCAGTGATCC[C/G]AAGCCACAGGCTTGC	10043
rs555313670	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35326271	ATAAAAAGGTTCTTC[A/G]GTCAAATAAATCTTA	10043
rs555355800	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35326838	GGATCCCAGTCTTCT[A/G]GGAGAGAGGGCGGAA	10043
rs555408564	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35332259	AGGTGACTGAGGGGC[C/T]CCATCTGGTAGCAGC	10043
rs555423294	snp	A/C	1.64814e-05	0.00287061	intron-variant	TOM1	GRCh38.p7	22:35317869	TATGACTCCTGGTTT[A/C]TTCTCAGAGAAAGCC	10043
rs555496906	snp	C/T	0.00398564	0.0444627	intron-variant	TOM1	GRCh38.p7	22:35345172	ACCCACCTGGCCTTG[C/T]CTGGTTAACTTCGCG	10043
rs555498412	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35337294	GGCTGGGCATGGCTT[A/C]TTCAGCCTTGCCCAC	10043
rs555549699	snp	C/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334049	CTGATTACTGTCCTC[C/G]TGCCCAGCCACTTCC	10043
rs555588958	in-del	-/T	0.0023933	0.0345097	intron-variant	TOM1	GRCh38.p7	22:35339792	GCCTGTAGTCCCAGC[-/T]ACTTGGGAGGCTGAG	10043
rs555752369	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334566	CCTGCTTAGTAAGCA[C/T]GCCCTTAGTATCCCC	10043
rs555888147	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35325171	CAGGCCCATCACATC[C/T]GCGGAGCGTAAAGGT	10043
rs555978102	snp	C/T	1.6795e-05	0.0028978	intron-variant	TOM1	GRCh38.p7	22:35322089	CGGTCCACTGAAAGT[C/T]ACCTCCCCTCAGACC	10043
rs555986955	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	TOM1	GRCh38.p7	22:35297906	AGCTTAAAGGAAGGG[C/G]CAGAGATGGTGGCTC	10043
rs555998112	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35318566	AGGATTGGGGTCTTG[A/G]CCTCCAATGTCTGAC	10043
rs556046133	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35304146	AGGGTTCCACAGCCA[C/T]TCAAGGTCAGAATCC	10043
rs556062081	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	TOM1	GRCh38.p7	22:35299097	TTTTCTTCAGAAAGG[C/T]TCATGGCTTTTGTCA	10043
rs556109246	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35340392	TGAGGTGGAGGCCGC[A/G]GGGAAGTCTTGAGCA	10043
rs556125327	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35305017	TGGAGGGGAAAAGTG[A/T]AAAAGTCAGAGAGAG	10043
rs556225198	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35316247	TCACCCTTAAAAGGC[A/G]GAGCAAAGCCTGTCT	10043
rs556501764	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1	GRCh38.p7	22:35311358	AAACCACCACAACAA[C/T]GCACTTTGTTTACCT	10043
rs556525022	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35324383	CCAGGAGTTTGAGAC[C/T]AGGCTGGGCAACATA	10043
rs556567438	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35329848	GTGGATTAAATTTTA[A/G]CATCTAACACTTGGA	10043
rs556633791	snp	C/G	6.89917e-05	0.00587291	intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	TOM1	GRCh38.p7	22:35299880	GTCGGTGGCGCTGGC[C/G]GTTGCTGTCAGCTGA	10043
rs556641402	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35313204	ATACAAAACTTAGCC[A/T]GGTGTGTTGGCAGGT	10043
rs556643652	snp	A/G	0.00279162	0.0372561	intron-variant	TOM1	GRCh38.p7	22:35306449	TTCTGTCTTGAGGAT[A/G]ACAGAGCTTTGTCTA	10043
rs556724944	snp	C/T	0.0233782	0.105558	intron-variant	TOM1	GRCh38.p7	22:35331343	TCTCAAACTCTTGGC[C/T]TCAAGCAGTCCTCCC	10043
rs556746249	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35318221	ATTCCACACGGATCT[A/G]GAAGCCCAGCCTTGT	10043
rs556747946	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35331276	AATTTTCTTTTCTTT[C/T]TTTTTTTTTCTTTTT	10043
rs556806233	in-del	-/AC			intron-variant	TOM1	GRCh38.p7	22:35342833	TACACAGACACCCCT[-/AC]ACACACACCACACCT	10043
rs556824863	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1	GRCh38.p7	22:35347853	CCCCTCCGCTGCCTT[A/G]CCCTCCATCCTTCCT	10043
rs556835426	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35330581	TCTGAGCCTTCTCTC[A/G]TCCTCCTCTCAAACA	10043
rs556874366	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	TOM1, MIR3909	GRCh38.p7	22:35336118	TCATCTTTGAAACTG[C/T]CTTCAGCTGAGCACA	10043
rs556895619	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35300894	ACATGGCCAGTGCCA[C/T]ATAAAAAAAAACAGT	10043
rs556897300	snp	A/G	0.00159617	0.0282053	intron-variant	TOM1	GRCh38.p7	22:35318559	TGGGGGAAGGATTGG[A/G]GTCTTGGCCTCCAAT	10043
rs556975943	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	TOM1, MIR6069	GRCh38.p7	22:35336628	TTTGTCCGCATCTTC[A/G]TCAGTGCTGCTGTAC	10043
rs556992298	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35301448	ATGAGAACCGACATG[A/C]CTTCACCCAAACAGC	10043
rs557090766	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35325434	ATTAACGCACTGCCC[A/G]TTTGCCCCAAGAATA	10043
rs557104432	snp	A/G	0.00199481	0.0315187	intron-variant	TOM1	GRCh38.p7	22:35319949	TCTGCCTTCACTCCT[A/G]CTGAGAACCAGTGCC	10043
rs557115228	in-del	-/A	0.00398564	0.0444627	intron-variant	TOM1	GRCh38.p7	22:35332606	CACACACACACACAC[-/A]TACACACACACAAAT	10043
rs557130241	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35317669	GAGCAGAGGTACTCC[A/G]GCCTCAGTGGCTACA	10043
rs557229872	snp	A/C/G	0.000199086	0.00997524	intron-variant	TOM1	GRCh38.p7	22:35323470	TGAGCTGTGGTTACC[A/C/G]GCTGTGTCCCCTTGT	10043
rs557417701	snp	C/T	0.00159617	0.0282053	intron-variant	TOM1	GRCh38.p7	22:35319305	TGCTATTTATTTGAG[C/T]ACTTTGTGTGTTCCA	10043
rs557492354	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35310227	CAGGTCCTGAGGATG[C/T]TGGAGGACAGATTAA	10043
rs557547762	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35339934	AGCGGACCCTAAAGC[A/G]GCGGGGAGAAATGCG	10043
rs557569028	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35302993	TCTTCTCAAGCCTGC[C/T]GACTCCCATGCCCTT	10043
rs557576392	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35302445	GGTTCAAGCGATTCT[C/T]CTGCCTCAGCCTCCC	10043
rs557602661	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35337820	GCCTCAAAGCTGCAC[G/T]GAGCCAGTGCTGAAG	10043
rs557638079	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35314684	GAGAGGCCTGCCGGT[A/G]GAGCTCAGGGAGGAG	10043
rs557739449	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35314705	CAGGGAGGAGAGGGC[C/T]AACTCCCTGTGTGGT	10043
rs557767717	snp	A/G	0.00199481	0.0315187	intron-variant	TOM1	GRCh38.p7	22:35304332	CTCATCGATGAGTAG[A/G]GGAGCTTCCCAAGGG	10043
rs557799756	snp	A/G	0.00019913	0.00997625	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35333467	GACCCAGCAGCCACC[A/G]GCAACCTCTCATCCC	10043
rs557831070	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35310734	AGCAAACAGGTACTG[C/T]AGGTTTATCATGGCC	10043
rs557831705	snp	A/C	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35338642	GTCAATCTGTGCCCC[A/C]CAGCCCGCTCCGTTC	10043
rs557848243	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	TOM1	GRCh38.p7	22:35298068	CCAAAAGAAGTTCAT[A/G]CTAAACATAACTCCA	10043
rs557875094	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35344957	TCAGAGTCACACTGT[A/G]TTAAGGGGTGAGCTA	10043
rs557880323	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35322489	GGGCGGCCAGACACA[C/T]GTGGGCCTCCTAGCC	10043
rs557899682	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35316086	CAGATAATAGACAGC[C/T]GGCAGCACTGTGCTC	10043
rs557904640	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35328868	ACCCAGGCACCTGCC[A/G]TGACCCAGGAACCTT	10043
rs557941872	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35328523	CTGGTAAGTAGCAGA[A/G]CTGCGATTTGAACCC	10043
rs558082408	snp	C/G	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35315780	CTGGCTAGAAGAGGG[C/G]CCTGTCCAGTCCCGC	10043
rs558199059	snp	G/T	0.00143343	0.0267331	intron-variant	TOM1	GRCh38.p7	22:35323641	AGAGGGTGAGAGAAC[G/T]GCCGTACCGGGAACC	10043
rs558217681	snp	C/T	1.66059e-05	0.00288144	missense, nc-transcript-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35323151	CCACCCACCATCGTG[C/T]ATGACAAAGTGCTCA	10043
rs558404663	snp	C/T			upstream-variant-2KB	TOM1	GRCh38.p7	22:35298377	GTACAGTAAAGACAT[C/T]GGACCCCATGGCTGC	10043
rs558421255	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1	GRCh38.p7	22:35347634	CCACAGTGGAAATTC[G/T]GCCGAGCCTCTTGTC	10043
rs558453690	snp	A/C/G	8.31339e-05	0.00644681	synonymous-codon, missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35346953	TGCGGAAGAGCCTAA[A/C/G]GGGGTCACCAGCGAA	10043
rs558464668	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35340233	TGGTGGACCTGGGGC[C/T]GAGGAGGCTAGAGGA	10043
rs558562256	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35341034	AGCACATTGCACACC[C/T]GTGTCACATCCACCG	10043
rs558577716	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35312535	GACTTCTCTGGCTTT[A/G]AATCTGCTGTGCATC	10043
rs558702826	snp	C/T	0.00199481	0.0315187	intron-variant	TOM1	GRCh38.p7	22:35305389	ATGGCGGGCCAGGCA[C/T]GGTGGCTCACGCCTG	10043
rs558718871	snp	A/T	0.00159617	0.0282053	intron-variant	TOM1	GRCh38.p7	22:35341477	GAGTGAGTGGAGGTG[A/T]GTGTCTCCCTCCTCA	10043
rs558759981	snp	A/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	TOM1, MIR3909	GRCh38.p7	22:35335857	GGTACTCAGAGCTGG[A/T]CCAGGTGCTGGGTGA	10043
rs558761269	snp	A/C	0.00874735	0.0655527	intron-variant	TOM1	GRCh38.p7	22:35300193	TGATAGATGTATATG[A/C]CAGCCAGTAGGTAAG	10043
rs558817377	snp	A/C			intron-variant	TOM1	GRCh38.p7	22:35329831	CATGTTGATGGTTTC[A/C]TGTGGATTAAATTTT	10043
rs558820594	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35314551	CCACTTACTTGCCTT[G/T]CCAAAACAACCACAG	10043
rs558826299	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35306238	TATGGGTTCATAGTT[C/T]GCTGACTTCTGAATC	10043
rs558831291	snp	C/T			intron-variant, nc-transcript-variant	TOM1, MIR3909	GRCh38.p7	22:35335647	CTGGCTGAGGTATGC[C/T]GTTGCGCTGTCCTTC	10043
rs558848779	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35313693	GTCTTGCCATCATGC[C/T]AGGCAGATTATCTGG	10043
rs558889313	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1	GRCh38.p7	22:35324950	GCAGGTGGCACCCTG[A/G]GCATGTCACTTCCTT	10043
rs558893704	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35305677	AAAAAAAAAAAAACT[A/G]ATGGGTGCTGGGGAG	10043
rs559043579	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35304200	CTCACCACACTGCCT[C/T]GAGCTGCCCAGTGCT	10043
rs559069455	snp	A/T	0.00159617	0.0282053	intron-variant	TOM1	GRCh38.p7	22:35330030	CACGCCTGTAATCCC[A/T]GCACTTTGGGAGGCC	10043
rs559089902	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35330706	GGGTTAGCGCTGCTG[C/T]CTGTGCCCAAGTCCA	10043
rs559154916	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35313245	CCAGCTACTCGGGAG[A/G]CTGAGGCAGGAGAAT	10043
rs559162879	snp	A/C			intron-variant	TOM1	GRCh38.p7	22:35319872	GTGTCCCTTCCACCG[A/C]AGGCCTGACCGCCTC	10043
rs559175607	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	TOM1, MIR3909	GRCh38.p7	22:35336193	CAGGCCCTCCCCAGG[A/G]CTTGGTTTCCACCCT	10043
rs559215372	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35318764	TGGGCAGAGGTGTGG[A/G]AGCCGTGGGCAGCAG	10043
rs559220901	snp	A/T	0.00119737	0.0244387	intron-variant	TOM1	GRCh38.p7	22:35319240	GGACAGCAAGCCCCC[A/T]TGTCCCTTATAAACA	10043
rs559376152	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35343570	ACCTACACACACCAC[A/G]CCTACACTCATACAC	10043
rs559391542	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35330209	GAATGGCATGAACCC[A/G]GGACACAGCTTGCAG	10043
rs559402299	snp	C/T			stop-gained, nc-transcript-variant, intron-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35321975	CCCAAAGATGCCCTC[C/T]GAGCAGTAAAGAAGA	10043
rs559430297	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	TOM1, MIR3909	GRCh38.p7	22:35335680	CTGGGGAGCAGGCTC[C/T]GGGGGACAGGGAAAA	10043
rs559535456	in-del	-/C	0.00159617	0.0282053	intron-variant	TOM1	GRCh38.p7	22:35346585	GGAAAGGAACCAGCA[-/C]TCATCAAGGTCCCAC	10043
rs559603709	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35308081	GGAACTTGGCCAGCA[A/G]GCTCCCCTTGTCCTT	10043
rs559789539	snp	G/T	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35332386	ACTTCAGGGAGGCAG[G/T]TGCCTACAGATACTA	10043
rs559824386	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35337388	CTCTGGGTCAGAAGT[C/T]AGCAACCTGACGCCC	10043
rs559865154	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35326971	CCTCCAGGGCCTTGT[C/T]AGCTGCTGTGTTAGA	10043
rs559896700	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB	TOM1	GRCh38.p7	22:35297609	TACAGGCGCCCACCA[C/T]GGCGCCCACCACCAC	10043
rs559901895	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35332884	TCATAACCCACCGTG[C/T]TGATGTTGAGACCCA	10043
rs559925778	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35315186	GGGAGGATGGTGGCC[A/G]GGCTGGGGCAGGGGC	10043
rs560284587	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35320916	GAGCCCAGGAGTTCC[A/G]GGCTACAGCGAGCTG	10043
rs560376730	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35327642	GCTCTAACAATAGCC[C/T]TCATGGCACAAGTTT	10043
rs560405125	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35339057	GAGACCAGGCCGGGC[A/G]TGGTGGCTCACACCT	10043
rs560411674	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35333698	CACAAGTCCTGAGCC[A/G]CCTTGGATCTCAGAA	10043
rs560447875	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35345490	GGGAAGGAGCTCCCT[C/G]TGACCCCTGGCCCTG	10043
rs560556701	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1	GRCh38.p7	22:35311229	GCCGTAGTTGTCCAC[C/T]GCGGAGCAGTCCCGT	10043
rs560571917	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35341105	GCCATCATTTGCTGA[A/G]CCTGTGCTCCGGGCC	10043
rs560628637	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334157	CTGGGAAGAGGAAGC[C/T]GCTTGCCCAAGGCCC	10043
rs560652383	snp	C/T	1.67049e-05	0.00289002	intron-variant	TOM1	GRCh38.p7	22:35346993	CCCCGCCCCTGCCCG[C/T]CCTCTCCTTTCCCCA	10043
rs560782116	snp	C/T	0.000100271	0.00707992	intron-variant	TOM1	GRCh38.p7	22:35346995	CCGCCCCTGCCCGCC[C/T]TCTCCTTTCCCCAGG	10043
rs560882212	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35335063	CAGCAGCATAGGCAC[A/G]TGGCCTGAGTGTGTC	10043
rs560888779	snp	A/C/T	0.000147186	0.00857737	intron-variant	TOM1	GRCh38.p7	22:35323966	CAGGTGGGCCACACA[A/C/T]GTCAGGGAGGGCCCC	10043
rs560912011	snp	A/T	0.00199481	0.0315187	intron-variant	TOM1	GRCh38.p7	22:35303032	TAGAGCTGTAGAGCC[A/T]TATGGAATTGACATC	10043
rs561063353	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35304452	GATATTCTCTGCAGA[C/T]AAATCTTACTGGATC	10043
rs561085331	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35346683	GTTAGCTTCAGCCCC[C/T]ACCCCGCCCCCATTT	10043
rs561099626	snp	C/G			intron-variant	TOM1	GRCh38.p7	22:35303090	ATCAGGAATGAGTGT[C/G]AGTCACTGGAATCAC	10043
rs561143777	snp	C/T	4.98144e-05	0.00499047	intron-variant	TOM1	GRCh38.p7	22:35323469	GTGAGCTGTGGTTAC[C/T]GGCTGTGTCCCCTTG	10043
rs561236378	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35313302	CAGTGAGCCAAGATC[A/G]TGCCACTGTACTCCA	10043
rs561239059	snp	A/C/G	0.000136191	0.00825107	intron-variant, nc-transcript-variant	TOM1	GRCh38.p7	22:35323005	CTGACCAAGGTGCTC[A/C/G]ACGGCACCTCTCGGC	10043
rs561302929	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35319597	TAGGAGGCTTCTTCT[C/T]TCCCAGGGTGGGCCC	10043
rs561362539	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1	GRCh38.p7	22:35318352	ACTCCGGCTTTTCTG[C/T]GAGCAAAAACAGACT	10043
rs561368399	snp	G/T	0.0023933	0.0345097	intron-variant	TOM1	GRCh38.p7	22:35301206	TACTCCAGCCTGGAC[G/T]ACGCAGGGAGAGCCC	10043
rs561432278	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35307458	TTTGATCACTGGGAC[A/G]TAAGCAGCCTGAAAT	10043
rs561509391	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35339160	ACATGGTGAAACCCC[A/G]TATCTACTAAAAATA	10043
rs561576819	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35314341	TATCCCCTCCCACCC[C/T]GCAGAAAACCTCCGT	10043
rs561622708	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35331503	CAGCTGGGGTATGGG[A/G]GAGGGCCCTTTGATG	10043
rs561642126	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35313936	TACAGCTCCGAGGTC[A/G]GGGAATCAGTTGTCA	10043
rs561678384	in-del	-/CAC	0.0126979	0.078662	intron-variant	TOM1	GRCh38.p7	22:35343133	CACACACCACACACA[-/CAC]ATCTACACCCACCAC	10043
rs561769937	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35332501	CACTAAAGTCTTCTC[A/G]ATCTATCACACCGGC	10043
rs561818238	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35325011	CTTGTGGAGTGCCAT[G/T]GCTGCTGTATCTGCT	10043
rs561822182	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35306531	TGAGTCAGACTGAAT[A/G]GTCTGAGTCCTGGTT	10043
rs562077789	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35332928	TCTGCCTGGCCGTGT[G/T]TGGGGGCCTGTCTCA	10043
rs562091574	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35344182	CCCTCCGCCATCAGC[A/G]TGACTCTCTCTCACC	10043
rs562107802	snp	A/C			intron-variant	TOM1	GRCh38.p7	22:35311668	AGAGGCAGTCTTCAC[A/C]GGGACAGAGCAGAGT	10043
rs562118669	snp	C/G			intron-variant	TOM1	GRCh38.p7	22:35331506	CTGGGGTATGGGAGA[C/G]GGCCCTTTGATGGCA	10043
rs562123750	in-del	-/A			intron-variant	TOM1	GRCh38.p7	22:35339649	GTGGCTCACGCCTGT[-/A]ATCCCAGCACTTTGG	10043
rs562155795	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35340788	CGAGTTGTGGAAACC[A/G]TCCAGGCCAGTCCAC	10043
rs562218125	snp	A/G	0.00557542	0.0525036	intron-variant	TOM1	GRCh38.p7	22:35315287	TGTGGCTAGGGAGGG[A/G]GATGACACTAATCCT	10043
rs562263177	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35321556	GGGTCATACCACCAC[A/G]CCCGGCAAATTTTTG	10043
rs562315610	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35327457	CATGCATTCTTTCCC[A/G]ATCCTCATGACAGTC	10043
rs562330339	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35345637	GGGTGGGAGGCTGCC[C/T]AGGGCCACCCAGCTG	10043
rs562349672	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35313935	TTACAGCTCCGAGGT[C/T]GGGGAATCAGTTGTC	10043
rs562356833	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35305608	AAGGTTGCAGTGAGC[C/T]AAGATCACGCCGCTG	10043
rs562433287	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35311019	TGGGCTTAGGAGCAC[A/G]AGTTGAGGTGGGGAG	10043
rs562498146	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35310367	AGACCATCCTGGCCA[A/G]TGTGGTGAAACCCTG	10043
rs562561006	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35315917	CCCAGTGCCTGGAAC[C/T]GGCTTGGCTTACAAA	10043
rs562588594	snp	C/T	0.00199481	0.0315187	intron-variant	TOM1	GRCh38.p7	22:35328743	ACAGGGTCCACATGA[C/T]AGCCAAAATAAACAC	10043
rs562771331	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35312170	AATTGCTTAAACCCA[G/T]GAGACGGAAGTTGCA	10043
rs562805671	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35304456	TTCTCTGCAGACAAA[C/T]CTTACTGGATCTGTT	10043
rs562819229	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35339088	GTAATCCCAGCACTT[C/T]GGGAGGCTGAGGCGG	10043
rs562850459	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35345982	CCTGGGCACAGTAGC[C/T]TCTCGGCTGCTTCCC	10043
rs562913531	snp	G/T			intron-variant	TOM1	GRCh38.p7	22:35311412	GTTTCAGGGTGGGTT[G/T]GACAGCTCCACGATG	10043
rs562967919	snp	C/T	0.00597247	0.0543191	intron-variant, nc-transcript-variant	TOM1, MIR3909	GRCh38.p7	22:35335652	TGAGGTATGCTGTTG[C/T]GCTGTCCTTCCTCTG	10043
rs562968264	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35329455	TTACCAGTTTTGACA[A/G]ATGCCAGACTAAGGG	10043
rs562993784	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35346761	AGGTCCTACGGCTCA[A/G]GGAGGAGCCCAGGTC	10043
rs563004983	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35335090	TGTCCACCAGGGTCT[G/T]ACCCCTTGCCGGGAC	10043
rs563056675	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35307237	TTCATTATTATTTTC[A/G]TAGGGTTTTCTTTTC	10043
rs563106277	in-del	-/AAAG	0.00279162	0.0372561	intron-variant	TOM1	GRCh38.p7	22:35313354	TGTCTCAAAAAAAAA[-/AAAG]AAAGAAAGGGGTGAT	10043
rs563180006	snp	A/G	0.00279162	0.0372561	intron-variant	TOM1	GRCh38.p7	22:35300313	GACTGCGTGGTTGGC[A/G]GTGGCTGGGCCACTC	10043
rs563182740	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35343816	CCCACACCTACACCT[A/G]CACATACACACCTAC	10043
rs563196809	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35341693	CACAGCAATTCAGGC[A/G]TGACTAAAACTAGAG	10043
rs563281685	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35330144	AAAAAATTAGCCAGG[C/T]GTGGTGGCAGACGCC	10043
rs563291134	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35318875	CCAGCTCTCCCGCGG[A/C]CAGTGCAGGGTTCCT	10043
rs563402595	snp	C/G	8.38118e-05	0.00647293	intron-variant	TOM1	GRCh38.p7	22:35300002	CCCTGGAGCCCCCCA[C/G]AGCTCCGCCCCGGTG	10043
rs563419774	snp	G/T			intron-variant	TOM1	GRCh38.p7	22:35345337	CCTGGGGTCTGACCC[G/T]GGGCTTGGCGTGTCT	10043
rs563424320	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1	GRCh38.p7	22:35313010	AGGATGGGAGCGAGC[A/G]GGCTCCAGGCTGCTT	10043
rs563445227	snp	A/G	0.0126979	0.078662	intron-variant	TOM1	GRCh38.p7	22:35341252	TGAAACCACAGGTGT[A/G]CTGTCCTCGGTATGG	10043
rs563485512	in-del	-/A	0.00279162	0.0372561	intron-variant	TOM1	GRCh38.p7	22:35344219	GGAGGCGGCTGCGGG[-/A]AAAGCCTCAGTGACT	10043
rs563512183	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35318500	TGTTGGGGTCACGGT[A/T]TCGTCTTGCTCAGTG	10043
rs563586265	snp	G/T	0.00676609	0.0577691	intron-variant	TOM1	GRCh38.p7	22:35344918	GACGAGGGAAATCAG[G/T]CGCAGAGAAGTTAAG	10043
rs563658416	in-del	-/TG			intron-variant	TOM1	GRCh38.p7	22:35308214	GCTCGCTCTTTCTCC[-/TG]TGTGTGTGTGTGTGT	10043
rs563663228	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35301264	CACACACACGCACAC[A/G]TATATATAAAAATAT	10043
rs563698705	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35307537	GCTCCGCCCCTTCCC[A/G]GCTGTGTCCCCCAGG	10043
rs563700786	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35313862	GAGGATTGCAGGGCC[C/T]GGTTCTGTCAGGAGC	10043
rs563828146	snp	A/G	0.00279162	0.0372561	intron-variant	TOM1	GRCh38.p7	22:35301777	TCCTGAACCAGGGAG[A/G]GGAACTGCCCTCTCA	10043
rs563854870	snp	C/T	0.00279162	0.0372561	intron-variant	TOM1	GRCh38.p7	22:35343459	ACACACACCTACACA[C/T]ACACATTCATACACC	10043
rs563873970	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35331610	GGAGAAGGGCTGGGC[A/G]CAGTGGCTCACACCT	10043
rs563938231	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35320293	TCAGGAGCCTTCAGG[G/T]TGCAAGTGGGGGCCC	10043
rs563967585	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35302627	ATGACCACCGTGTCC[A/G]GCCTAGAATGTGAAT	10043
rs563967703	snp	A/G	0.0023933	0.0345097	intron-variant	TOM1	GRCh38.p7	22:35309523	GTGGTGGGCGCCTGT[A/G]ATCCCAGCTACCCTG	10043
rs564036745	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	TOM1, MIR6069	GRCh38.p7	22:35336374	GCCCGCTCCTCCCTG[C/T]ACCTGCCTGGCTCCC	10043
rs564061142	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35320730	TTCTTTGGATCTCCC[C/T]GCAAGGTGGGGAGGA	10043
rs564102813	snp	C/G	0.00119737	0.0244387	intron-variant	TOM1	GRCh38.p7	22:35327537	CCAGGGACTTTGGAC[C/G]CCATCAGATTGGAAT	10043
rs564141533	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35327059	GGTAACGGTTGGTAG[C/T]GCCTCTGTGAGGGGT	10043
rs564205007	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35332293	TACCCTCAGATATCC[A/G]CAGTCATTAGGCTTA	10043
rs564205079	snp	C/T	0.00199481	0.0315187	intron-variant	TOM1	GRCh38.p7	22:35310325	TTTGGGAGGCCAAGA[C/T]GGGTGGATCACGAGG	10043
rs564231662	snp	A/G	0.00279162	0.0372561	intron-variant	TOM1	GRCh38.p7	22:35333184	TTTAAGGTAAATAAG[A/G]CTGTGCCACCACCTG	10043
rs564293952	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35314277	GATCTGCCTTGTCCC[A/G]ATTTTGTCTCCTCCT	10043
rs564376557	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35322219	GCAAGAGGCCATTTG[A/G]AAAGGTTCTCCCCAA	10043
rs564409626	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35311231	CGTAGTTGTCCACCG[C/T]GGAGCAGTCCCGTGG	10043
rs564481858	in-del	-/T			intron-variant	TOM1	GRCh38.p7	22:35317247	TTGTCCAGGCTGGAG[-/T]GTGATGGCTCAATCT	10043
rs564506270	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35333673	TCGGGGTCACTGCCC[C/T]TGGCAGCCCCACAAG	10043
rs564548049	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	TOM1	GRCh38.p7	22:35297581	CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC	10043
rs564593783	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35346014	GAGCCTGCTCCCAAG[G/T]TGAGGTCCCAGTGGG	10043
rs564595102	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35338890	GCACTGGCCCAGCAC[A/G]TCCACAGGCCCTTCC	10043
rs564598591	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35345235	TATCATGAAATCTGC[A/G]TCTGCAGAGACACCA	10043
rs564637904	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35301884	GCTCTCCTCTCATCT[A/G]TATTTCTCTGACTAC	10043
rs564675610	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35316399	TAGCATCTAGGAAGG[C/T]GCAGAGAACAGAAAA	10043
rs564710333	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	TOM1	GRCh38.p7	22:35298467	AGACACAGCCTTACT[C/G]TGTCACCCAGGCTGG	10043
rs564745885	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35339936	CGGACCCTAAAGCAG[C/T]GGGGAGAAATGCGAG	10043
rs564754303	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35311431	AGCTCCACGATGTCT[C/T]AAAACAGCCAGACTC	10043
rs564840719	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35305202	GGACACCTGGTTCCA[A/G]CTCTGGTTCTGCTCC	10043
rs564921904	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35346379	TTCAGGCCCAGAAGC[C/T]GCCTTCTGCAGGTGA	10043
rs564932818	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35335025	CCCTTCCCTGTGCAC[C/T]GTGCATTTTCAGGGG	10043
rs565021219	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35320148	GCCCTATAGCAAGCT[G/T]CTTCTCTACCCAGGG	10043
rs565033097	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35322860	GTAAACAAGTCCCCC[A/G]GTCCTGGCATTGTCC	10043
rs565038987	snp	C/T	0.00159617	0.0282053	intron-variant	TOM1	GRCh38.p7	22:35329202	CTCAGGTGATCCACC[C/T]GCCTCGGCCTCCCCA	10043
rs565064824	snp	C/G			intron-variant	TOM1	GRCh38.p7	22:35322184	ACTGTCCTGTCTACA[C/G]TGCAGGCGGATGCAG	10043
rs565074738	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35328700	CGATGAGGAAATCCC[A/G]GAGGCCTGACCTTGG	10043
rs565124128	snp	A/G	0.0023933	0.0345097	intron-variant	TOM1	GRCh38.p7	22:35307798	AATTTAGGGACAGAC[A/G]GAGGGGTCTACTGTT	10043
rs565173748	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334620	GAGCCCTGTGGTCAG[C/T]TGACAGACTGCGCTC	10043
rs565182681	snp	A/G	0.00318978	0.0398085	intron-variant	TOM1	GRCh38.p7	22:35322234	GAAAGGTTCTCCCCA[A/G]TCCCCCAGCATGGGA	10043
rs565185036	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35306667	TGTCGTGTTGTTGTG[C/T]TATAAAGCACTTCCT	10043
rs565195255	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35317195	ATTCTTTTTTGCTTG[C/T]TTGTTTGTTTGTTTT	10043
rs565249623	snp	A/G	0.00438332	0.0466095	intron-variant	TOM1	GRCh38.p7	22:35305968	AATACTTGTGGCTTC[A/G]TGAACCAGATGGTCT	10043
rs565254933	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35312196	TTGCAGTGAGCCGAG[A/G]TCGCACCACTGTACT	10043
rs565296661	snp	C/T	0.00597247	0.0543191	intron-variant	TOM1	GRCh38.p7	22:35318611	CAGCCGTGTGACCTT[C/T]GGAAGTCACTTTACC	10043
rs565339927	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35324080	ATGAGACTCAGAGAG[A/G]TCCATTCACTTGCCC	10043
rs565429899	snp	A/G	1.64895e-05	0.00287132	intron-variant	TOM1	GRCh38.p7	22:35323663	CCGGGAACCAAGGGA[A/G]GGGAGGCAGGACTCA	10043
rs565450803	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35312781	AGGGCAAGCCACATA[A/G]AGGAAGGGGGTACAG	10043
rs565492137	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35316841	ATTTTGGGCCCGTAC[C/T]GTGCTGATACCTTGC	10043
rs565499076	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35339835	CGTGAACCCAGGAGG[C/T]GGAGCTTGCAGTGAG	10043
rs565530216	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	TOM1	GRCh38.p7	22:35348036	GCCTCACAGAGGCAG[C/T]GACTACTTTGGGCAG	10043
rs565611100	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	TOM1	GRCh38.p7	22:35348237	CCTCAAGGCACCTTC[A/G]TGCTGCTGTTCCATG	10043
rs565621448	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35314592	AACACTGATGTTCCC[C/T]CCTCCAGGAGATGAG	10043
rs565691103	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35318170	CTGGCCCCTGGGGGC[C/T]GCCACCCCACCCCGC	10043
rs565693682	in-del	-/AC	0.00318978	0.0398085	intron-variant	TOM1	GRCh38.p7	22:35326753	TCTAGGAGGAGAGAG[-/AC]GGCGGGATCCCAGTC	10043
rs565841553	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35307594	TTAGAAGTTGATAGA[A/G]CACTGCAAAGTGCGG	10043
rs565848221	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35300742	GTGACAGGATACTCA[C/G]AGTTCTGTGACGCAG	10043
rs565877283	snp	G/T	0.00119737	0.0244387	intron-variant	TOM1	GRCh38.p7	22:35342859	ACACCTACACACTCA[G/T]GCACCTACACACACC	10043
rs565941521	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35326819	TAGGAGGAGAGAGAG[A/G]GGGGGATCCCAGTCT	10043
rs565958438	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35330973	TCCCAACAGAACAAG[A/G]AAGATGGATCCCAGG	10043
rs565995191	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	TOM1, MIR6069	GRCh38.p7	22:35336497	CTGGCACCGTCACAG[C/T]CTTCCTGCAGCCAGT	10043
rs566002656	snp	C/T	0.00142757	0.0266786	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35347136	CAGCTGAGGGGCCCC[C/T]GGGTCCCCCATCTGG	10043
rs566163547	snp	C/T	0.0244538	0.107838	intron-variant	TOM1	GRCh38.p7	22:35302336	TTTCTTTTTCTTTTT[C/T]TTTTTTTTTTTTTTT	10043
rs566191344	snp	A/T	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35301273	GCACACATATATATA[A/T]AAATATACACATACA	10043
rs566297245	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35319871	CGTGTCCCTTCCACC[A/G]CAGGCCTGACCGCCT	10043
rs566358550	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35319262	TTATAAACATGGGAG[A/G]AACAGGCTCGGCGTC	10043
rs566388432	in-del	-/CCTACACACACC	0.0174175	0.0916809	intron-variant	TOM1	GRCh38.p7	22:35343585	ACCTACACTCATACA[-/CCTACACACACC]CCTACACACACCACA	10043
rs566407486	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35325223	GAGTTAGACACGGAT[A/G]TGTGATGGAAAGAAA	10043
rs566429562	snp	G/T			stop-gained, nc-transcript-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35323097	AGCCAGGACTTCGTG[G/T]AGAGTGTGCTGGTGA	10043
rs566458763	snp	A/G	0.00199481	0.0315187	intron-variant	TOM1	GRCh38.p7	22:35344282	CAGGCCCGGCCACCC[A/G]GAAAGCTGGGGGTGC	10043
rs566485966	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35315985	GAGCCGGGGCACAGC[C/T]GTGAGGAGAGAGCCT	10043
rs566493742	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35309036	ACAAGTTTCTGGCTG[A/G]AAAAAAAATAGCTTC	10043
rs566546996	snp	C/T	0.000240067	0.0109534	intron-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35321750	CTCAAAGTGACTCTG[C/T]TGCTGGAGGTCCAGG	10043
rs566569885	snp	G/T	0.00159617	0.0282053	intron-variant	TOM1	GRCh38.p7	22:35326820	AGGAGGAGAGAGAGG[G/T]GGGGATCCCAGTCTT	10043
rs566607942	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35321264	ACCCTTGGGGAGCAT[A/G]AGAAGCATTCAGATT	10043
rs566706490	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35339379	CCGGGCTTCACATTC[C/T]AGCTCTACCAGTTAC	10043
rs566730261	snp	A/T	0.00358779	0.0422022	intron-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35338429	GCACTGGAGCTATTT[A/T]TCAGTCTCCTGAGTT	10043
rs566792976	snp	A/G	0.000610616	0.0174624	synonymous-codon, nc-transcript-variant	TOM1	GRCh38.p7	22:35345772	CATCGAGCAGTGGCT[A/G]TCCACTGACGTGGTA	10043
rs566805416	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35305301	CCTCTGCTTCCCAGA[A/G]GATTGGTAAGGAACG	10043
rs566922364	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35304580	ACCTCCCGGGTTCAC[A/G]CCATTCTCCTGCCTC	10043
rs567088312	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35304103	CCCATTTCACCAAAA[A/G]TCAGTCTAAGAGAAA	10043
rs567121305	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1	GRCh38.p7	22:35303688	TTTTTAGTAGAGATG[A/G]GGTTTCACCATGTTA	10043
rs567292993	snp	G/T			upstream-variant-2KB	TOM1	GRCh38.p7	22:35297719	CGTGATCTGCCTGCC[G/T]GGGTCTCCCAAAGTG	10043
rs567295340	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35333949	AATATAATTTACTGT[C/G]TGCTTCATGCCAAGC	10043
rs567313643	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334238	CCACTTCCCCAGCAC[C/G]AAGCCCTGGGTCTGG	10043
rs567349525	snp	A/G	0.00438332	0.0466095	intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	TOM1	GRCh38.p7	22:35299849	CTCGCCGGCCTCCGA[A/G]TGCGTCACGTGACGG	10043
rs567373958	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35309898	GCCCAAGAGACACCC[A/G]CTTCCATCTCTGTGG	10043
rs567379582	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	TOM1	GRCh38.p7	22:35298535	CCCCCCTGGGTCCAA[C/G]CAATTCTCATGCCTC	10043
rs567381698	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35346624	AGGTGCTGGGCTTGG[C/T]GTGCTGTGTGTTATC	10043
rs567387602	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35317734	CAGTCTCACACAGGG[C/T]CAGGCCCTGTGCCCA	10043
rs567481163	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35328780	GTGCCGAGCCTCAGC[A/G]TTGCCTCCAGGAGAA	10043
rs567489740	snp	C/G			intron-variant	TOM1	GRCh38.p7	22:35324315	GCTGGGCATGGTCAC[C/G]TGCGTCTGTGATCTT	10043
rs567519412	snp	A/G	0.00159617	0.0282053	intron-variant	TOM1	GRCh38.p7	22:35300088	AGGGAGGGCAAGGAG[A/G]CTGGCGTGTAGCTCT	10043
rs567545752	snp	C/T	0.0023933	0.0345097	intron-variant	TOM1	GRCh38.p7	22:35316829	TGCTGAGTGTTTATT[C/T]TGGGCCCGTACCGTG	10043
rs567608071	snp	A/G	0.00358779	0.0422022	intron-variant	TOM1	GRCh38.p7	22:35322360	GGGGGCAGGGAGGCC[A/G]GCTGACTGAGTTGGG	10043
rs567637763	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35326849	TTCTAGGAGAGAGGG[C/T]GGAATCCCAGTCCTC	10043
rs567735094	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35319061	TGTCTTCCTCAGCCC[C/T]GCTCCCTGATCTTGC	10043
rs567736352	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35340824	GCAAAGTCTTCGTGA[C/T]CCCCAAGGGCACTCT	10043
rs567741679	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35305511	CTAAAAATACAAAAA[G/T]TAGCTGGACGTGGTG	10043
rs567793262	snp	G/T	0.00199481	0.0315187	intron-variant	TOM1	GRCh38.p7	22:35318657	CCTCGAAGGTGCTCT[G/T]TTAGATCCTTCCAGC	10043
rs567871031	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35323709	CCAGGCTGGCCCCTG[A/C]CTTCCTGGGCTCTTG	10043
rs567898847	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	TOM1, MIR6069	GRCh38.p7	22:35336619	TTCCCCCGCTTTGTC[C/T]GCATCTTCGTCAGTG	10043
rs568003604	snp	G/T	0.0023933	0.0345097	intron-variant	TOM1	GRCh38.p7	22:35307282	TAAAATTTGACCTCA[G/T]CCTATATAATTATAT	10043
rs568043643	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	TOM1	GRCh38.p7	22:35348317	CTGTGTGGACTGTGT[A/G]CGCATGTGGGGTGCA	10043
rs568093426	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35330699	CTTTCCAGGGTTAGC[A/G]CTGCTGCCTGTGCCC	10043
rs568102443	snp	C/T			upstream-variant-2KB	TOM1	GRCh38.p7	22:35298475	CCTTACTCTGTCACC[C/T]AGGCTGGAGTGCAGT	10043
rs568181494	in-del	-/AG	0.00398564	0.0444627	intron-variant	TOM1	GRCh38.p7	22:35309626	TCCAGCCTGGGCAAC[-/AG]AGTGAGACTCCATCT	10043
rs568191826	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35301437	GCACCAACACCATGA[A/G]AACCGACATGCCTTC	10043
rs568213904	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35302092	GCCTTTCTTGGGCAA[A/G]AAATACTTCTGTGCA	10043
rs568264308	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35337172	CGATCTCCTGACCTC[A/G]TGATCCGCGCGCCTT	10043
rs568585911	snp	A/G			intron-variant, downstream-variant-500B	TOM1, MIR3909, MIR6069	GRCh38.p7	22:35336257	CTGAGCATCCATTTC[A/G]TCTTCCCTTTGTTCT	10043
rs568699041	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35319887	CAGGCCTGACCGCCT[C/G]CATAGCTCTAGCCCC	10043
rs568714472	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35320449	GGGCCTCCCAACACC[A/G]TGACCCCTAGGCTTC	10043
rs568771000	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35326694	GGAGAGAGAGAGGAC[A/G]GAATCCCAGTCCTCT	10043
rs568797887	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	TOM1	GRCh38.p7	22:35297277	GTCCCACCTACTCAA[C/G]AGGCTGAAGTGGGAA	10043
rs568847258	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35302953	TTCTGTAAACCAGGC[C/T]CCTCCTTGCTGCAGG	10043
rs568862700	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35311267	CCAGGGCAGCTGGAC[C/T]TCACTCCTTAAAGAG	10043
rs568907273	snp	C/T	0.00318978	0.0398085	intron-variant	TOM1	GRCh38.p7	22:35344899	CTGCTAGCCTCACCC[C/T]AAGGACGAGGGAAAT	10043
rs568923038	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35310638	GATCAATGAGTGCCC[A/G]AGTGTGGAGGTGTTT	10043
rs568926773	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35316585	GCAGCCAGTGGTCCC[A/G]GCCATGGCCCTGACA	10043
rs568946739	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35337760	TTCCTAACAGGAATC[A/G]CAGGCCTTTCCCTTT	10043
rs568958659	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35321415	CTGGAGTACAGTGGC[A/G]CAATCTCGGCTCTCA	10043
rs569184710	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35305417	CTGTAATCCCAGCAC[A/G]TTGGGAGGCCGAGGC	10043
rs569320598	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1	GRCh38.p7	22:35299504	CCCAGGGTAGGTGTG[C/T]AGTCACAGTGAGGTC	10043
rs569336033	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35336964	TTTTTTTTTTGAGCC[A/G]GAGTCTCGCTCTGTC	10043
rs569373391	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35321879	ATGGGCCAATAAGAA[C/G]TGTTCCAACTCTCCA	10043
rs569400907	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35328831	ACAGTCGGCAATGCC[A/G]GGCAGCTCCCTGGAC	10043
rs569438623	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334827	CAAAACACAGTGTCT[C/G]CACCCCCCGCCCCCC	10043
rs569465439	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	TOM1	GRCh38.p7	22:35298714	GTTGGGATTACAGGC[A/G]TGAGCCACCACACCT	10043
rs569494954	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1	GRCh38.p7	22:35347555	GTGATACCCTGCTCC[A/G]GGCCCATGCCCCAAG	10043
rs569519289	snp	G/T			intron-variant	TOM1	GRCh38.p7	22:35308005	TCAATAACATGGGTG[G/T]GCCTCGTCCAATCAG	10043
rs569523141	snp	C/T	0.00478085	0.0486577	intron-variant	TOM1	GRCh38.p7	22:35304733	ACCACCCACCTCGGC[C/T]TCCCAAAGTGCTGGG	10043
rs569555453	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35314450	GACTCATGCACGGGG[C/T]GGGGGCGGGGGGTCC	10043
rs569574238	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35346281	GGAGCAGAAGGGGCA[A/G]GGCCAGACTCAGCTT	10043
rs569825727	snp	C/G	0.00398564	0.0444627	intron-variant	TOM1	GRCh38.p7	22:35318052	GGAGCCCCTGCCCCA[C/G]CCCCATTGCTGCCAT	10043
rs569872293	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35312790	CACATAGAGGAAGGG[A/G]GTACAGCTGACTGTG	10043
rs569879059	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35312499	ATAGCATCGTGGTTA[C/T]GAATATGGACTTGAG	10043
rs569888560	snp	C/G	1.64833e-05	0.00287078	missense, intron-variant, nc-transcript-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35323533	GCTCGCCCGATCTGA[C/G]AGGTGTGGTCACCAT	10043
rs569965807	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	TOM1, MIR3909	GRCh38.p7	22:35335837	GAGCATGCAACTCTG[C/T]GGAGGGTACTCAGAG	10043
rs569971489	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35317522	CAAGGGAGAACATCT[C/T]ATCTACAGAAATGAA	10043
rs569977860	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1	GRCh38.p7	22:35300679	CGGGCCAAGCCAAGC[C/T]CAGGGCACCTGGCGC	10043
rs569983054	in-del	-/CA			intron-variant	TOM1	GRCh38.p7	22:35343548	CACATCTACACCCAC[-/CA]CACACACCTACACAC	10043
rs570017385	snp	A/G	0.00199481	0.0315187	intron-variant	TOM1	GRCh38.p7	22:35324003	GAATTTACCATCCAC[A/G]GAGCCTCCACTTCTT	10043
rs570087713	snp	C/T	0.00358779	0.0422022	intron-variant	TOM1	GRCh38.p7	22:35301527	AAACCATCGCATTAC[C/T]GTGAAATTACTCTTC	10043
rs570114722	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35335212	GAGCTGTGGGCAGCC[A/C]GGATTCTTATAGCTA	10043
rs570124851	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35300151	CTTGATTGACAAGAA[C/T]TTGGGCCATTAGGAA	10043
rs570148965	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35307685	TAGAGAAGGGAAGGA[C/T]GGAGCCTGGAGTCTT	10043
rs570264268	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35325131	CACTGTGGAGACACC[A/C]ACGTTAAAGGTGTTG	10043
rs570327374	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35332126	GACACTCACTGATTG[A/G]TTCTAAATCAGTGGA	10043
rs570351906	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35330842	ACAAGTGACTTCACT[A/G]CTGCAAGCTACACAA	10043
rs570408044	snp	C/T	0.00438332	0.0466095	intron-variant	TOM1	GRCh38.p7	22:35343189	ACACACACCACACCT[C/T]CACTCATACGCCTAC	10043
rs570453126	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35313622	GCCCACATTCTATGA[A/G]TTAGGTCAGGCCAGA	10043
rs570464329	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1	GRCh38.p7	22:35314111	TGCCTACCCTGTGGG[C/T]ATCTGAAGGAAATCC	10043
rs570601046	snp	C/T	0.00438332	0.0466095	intron-variant	TOM1	GRCh38.p7	22:35326757	GGAGGAGAGAGACGG[C/T]GGGATCCCAGTCCTC	10043
rs570606438	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35337193	CGCGCGCCTTGGCCT[C/T]CCAAAGTGCTGGGAT	10043
rs570639000	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35337594	ACTGCGTGGGAACTG[A/G]GGGTCATATTCAAGA	10043
rs570639274	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35332586	CTGAAGAGAGCACTA[A/G]CACACACACACACAC	10043
rs570692886	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35343921	CCCCTACACACACCA[A/C]ACACATCTACACACA	10043
rs570780220	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35320481	TCAGCCCTCCCCGAC[A/C]TCCCCCACACTCAGT	10043
rs570907417	snp	A/C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35312175	CTTAAACCCAGGAGA[A/C/T]GGAAGTTGCAGTGAG	10043
rs571030519	snp	C/T	0.0023933	0.0345097	intron-variant	TOM1	GRCh38.p7	22:35310502	GAGGTTGCAGTGAGC[C/T]GAGATCGTGCCACTG	10043
rs571052339	snp	C/G	1.65083e-05	0.00287296	intron-variant	TOM1	GRCh38.p7	22:35345689	CTTCCACCTTGTCAC[C/G]TAGGGCACTGCCTTA	10043
rs571077919	in-del	-/AT	0.00159617	0.0282053	intron-variant	TOM1	GRCh38.p7	22:35306169	CCCAACTATTTAAAA[-/AT]ATATAAAGACCATCT	10043
rs571090995	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1	GRCh38.p7	22:35309759	TTCTTCTGTATTTCT[A/G]CCTAACCTTCTTGAC	10043
rs571116633	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35314808	GCACCTGCGCCACAG[C/T]GTCAGCGGCTGCCCC	10043
rs571123711	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35315451	GGACACTTGTTTGGC[C/G]CGCTCTGTTCTTCCC	10043
rs571208836	snp	A/G	0.000316569	0.0125771	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35333488	CTCTCATCCCAGCTG[A/G]CAGGAATGAGTAAGT	10043
rs571261889	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	TOM1	GRCh38.p7	22:35297352	TACCACTGTACGCCA[A/G]CCTGGGTGACAGAGA	10043
rs571275162	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35339224	TAATCCCAGCTACTC[A/G]GGAGGCTAAAGCAGG	10043
rs571290397	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35309186	CACACATCCCTGGAA[A/G]GTGAGTGCTTTGGTC	10043
rs571297996	snp	A/C	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35338643	TCAATCTGTGCCCCC[A/C]AGCCCGCTCCGTTCT	10043
rs571327898	snp	C/G/T	0.000399281	0.0141238	upstream-variant-2KB	TOM1	GRCh38.p7	22:35297486	TTTGAGACGGAGTCT[C/G/T]GCTCTGTCTCCCAGG	10043
rs571373614	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35316088	GATAATAGACAGCCG[G/T]CAGCACTGTGCTCAA	10043
rs571489406	snp	C/G	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35322336	AGCTCAGTAAACCCA[C/G]GCCTCCGCGGGGGCA	10043
rs571526149	snp	C/G	0.00159617	0.0282053	intron-variant	TOM1	GRCh38.p7	22:35328901	CCTGGTGGCAGGTAC[C/G]TGAAGAAATAATTGA	10043
rs571530049	snp	A/G	0.00119737	0.0244387	intron-variant	TOM1	GRCh38.p7	22:35340234	GGTGGACCTGGGGCC[A/G]AGGAGGCTAGAGGAG	10043
rs571589539	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35311841	GACACTTCTTCACTG[A/C]ATGATGGCTGTCATT	10043
rs571614372	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1	GRCh38.p7	22:35299777	GGGCGGGACCCTGGC[A/G]TCTCAGGGCGGGGCT	10043
rs571647853	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35317358	CCATGCCCAGCTACT[G/T]TTTTGTAGTTAGTAA	10043
rs571653068	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35313982	GCAACCACTGTCCGT[A/G]TTTTTATTCCCCCTT	10043
rs571745443	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35346638	GCGTGCTGTGTGTTA[C/T]CCCATTTCAGCTTCC	10043
rs571838715	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35323258	TGGAGAGTCGAGGCC[A/G]TCGTGTTTGTCCCAG	10043
rs571949969	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35340774	AAAGCAGGGAGGGAC[A/G]AGTTGTGGAAACCGT	10043
rs571964905	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35312069	ACCAGCCTGGCCAAG[A/G]TGGTGAAACCTCATC	10043
rs571980128	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35341514	GGCTTCCAGTGTGTC[A/G]GGATTCATCGGAACC	10043
rs572016770	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35341035	GCACATTGCACACCC[A/G]TGTCACATCCACCGC	10043
rs572019153	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1	GRCh38.p7	22:35347638	AGTGGAAATTCTGCC[A/G]AGCCTCTTGTCCCTT	10043
rs572028293	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35317581	CAGGAATAAGCACAC[A/G]GAGGCCCACCTAGAT	10043
rs572028833	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35305712	GATAGAACTGAATGT[G/T]CAGGGCTCCAAGGGC	10043
rs572091395	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35311532	TAGGCAGGGGCAGTC[A/G]GCATCGAACTGAGCA	10043
rs572127163	snp	C/T			intron-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35337173	GATCTCCTGACCTCG[C/T]GATCCGCGCGCCTTG	10043
rs572130994	in-del	-/CGGGC	0.00119737	0.0244387	intron-variant	TOM1	GRCh38.p7	22:35300663	GGGCAGCCGGGAACT[-/CGGGC]CGGGCCAAGCCAAGC	10043
rs572131745	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35335408	CTGCCCTGGCTGTTA[C/G]CTGTATCTTTCTTTA	10043
rs572198442	snp	C/T	0.00398564	0.0444627	intron-variant	TOM1	GRCh38.p7	22:35300613	CAGTGGTCGGACAAA[C/T]CCTCCTGGTCAGCCC	10043
rs572265593	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35301160	TGGATCTGGGAGGTC[A/G]GGGCTGCAGTGAGCC	10043
rs572266531	snp	C/T	0.00279162	0.0372561	intron-variant	TOM1	GRCh38.p7	22:35314615	GAGATGAGAGGTGCC[C/T]ATCGTTTTCAGGGGG	10043
rs572275745	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35335055	GGTACTTTCAGCAGC[A/G]TAGGCACGTGGCCTG	10043
rs572367609	snp	C/T			intron-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35337759	GTTCCTAACAGGAAT[C/T]GCAGGCCTTTCCCTT	10043
rs572369052	snp	A/C	0.000247081	0.0111121	intron-variant, missense, nc-transcript-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35299938	GCAGCAATGGACTTT[A/C]TCCTGGGGAACCCGT	10043
rs572435797	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35343108	CACACCCATACACCA[C/T]ACACACCCACACACA	10043
rs572478144	snp	A/G	0.0023933	0.0345097	intron-variant	TOM1	GRCh38.p7	22:35318318	CTGCATTCTGCAGGC[A/G]GGAGTGTGTACTAGA	10043
rs572529174	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35323959	GTCCAGGCAGGTGGG[C/T]CACACACGTCAGGGA	10043
rs572559403	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35307839	TGTGTTGGTGCAGTA[A/T]AAACCCTGTAGTGGT	10043
rs572601289	snp	C/T	0.00199481	0.0315187	intron-variant	TOM1	GRCh38.p7	22:35301697	TGTCGGTGGCTCTTC[C/T]GAGGTTTTGTAATCA	10043
rs572620811	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35313743	ATCTGCACCAGACCC[A/C]ATAGGGAGAGGACAG	10043
rs572819706	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35318778	GGAGCCGTGGGCAGC[A/G]GGAAGTGCTGCCAGA	10043
rs572821230	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35336849	GTGCTTGGCCCTCCA[C/T]CACCACAGGCATGGC	10043
rs572846958	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35325627	ATTAAATGAGTGCTG[A/G]CAGCGAGCTGCACTT	10043
rs572901809	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35344532	CTGGCAGCTAAGAGG[C/T]GATGGGGATAGCGGA	10043
rs572980412	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1	GRCh38.p7	22:35343341	ACACCCCCACACACA[C/T]ACCACACACATCTAC	10043
rs572983057	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35314776	GCTGAGAGATGCGGA[C/T]GGCACAGAAGCCTCA	10043
rs572993437	snp	G/T			downstream-variant-500B	TOM1	GRCh38.p7	22:35348315	ACCTGTGTGGACTGT[G/T]TGCGCATGTGGGGTG	10043
rs573043999	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35320515	GCCTCCTCTTAGTTC[A/C]TCCAAGGCATCAAGC	10043
rs573144401	snp	A/G	0.00199481	0.0315187	intron-variant	TOM1	GRCh38.p7	22:35303053	AATTGACATCCCTCA[A/G]ATGGTGATTCTAATG	10043
rs573205595	snp	A/G/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35309370	TGAAAGAGGCCAGGC[A/G/T]CAGTGGCTCACACCT	10043
rs573212615	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35338178	AGGACATTTAGAAGA[A/G]CTGTAACCAAGCCAC	10043
rs573212879	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35345129	GAAAGTGAAATGTCC[C/G]CATCTGTAGCACCGC	10043
rs573235621	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35308629	ACAAAGCCCACTCCA[C/T]CCCTGACCATCCAGA	10043
rs573280151	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35324512	AAACATATGTACATT[A/G]TACCATGCTGCTTCC	10043
rs573431008	snp	G/T	0.00358779	0.0422022	intron-variant	TOM1	GRCh38.p7	22:35332891	CCACCGTGTTGATGT[G/T]GAGACCCACAGTTTG	10043
rs573614253	snp	C/G	0.00119737	0.0244387	intron-variant	TOM1	GRCh38.p7	22:35327879	CTAGTGGTTCCTGCT[C/G]CCGGGTGTCACATGG	10043
rs573620432	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35316365	AATTTCCTGTGTGCA[C/T]GTGGTTGACGCGTGA	10043
rs573623484	snp	C/G			intron-variant	TOM1	GRCh38.p7	22:35300782	GCCGAGGTTTCCTCA[C/G]CTGTAGTTGGCGGGC	10043
rs573682871	snp	A/G	1.6498e-05	0.00287206	intron-variant	TOM1	GRCh38.p7	22:35322042	TGGCTCTCACAGTGA[A/G]TGCCCCATCTGTCTG	10043
rs573689705	snp	C/T	0.00119737	0.0244387	intron-variant	TOM1	GRCh38.p7	22:35321650	GTGATCCACCTGCCT[C/T]AGCCTCCCAAAGTCC	10043
rs573743820	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35321518	ATTCTCCCGCCTCAA[C/T]CTCCCAAGTAGCTGG	10043
rs573750645	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35346441	GACCAAGGACTCAGG[C/G]TTTCTGTCTGGTGGC	10043
rs573763510	snp	G/T			intron-variant	TOM1	GRCh38.p7	22:35345539	TGGTCCCCTGCTTAG[G/T]CTCCTGGCTCTGCAC	10043
rs573772789	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35311332	ACAGGAAACGCAACC[A/T]GCAGAGTCTGAAACC	10043
rs573799984	snp	C/T			utr-variant-3-prime, nc-transcript-variant	TOM1	GRCh38.p7	22:35347664	CCCTTCCCTGCTCTG[C/T]TGCATGGGGCCCCAT	10043
rs573815119	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35345959	TTTGGCACGCCCCCC[A/C]GAGAAGTCCTGGGCA	10043
rs573899751	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35317668	AGAGCAGAGGTACTC[C/T]GGCCTCAGTGGCTAC	10043
rs573963779	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35328609	CAGAAGCAAAGCCAC[C/T]GTGTGCTTGGTCATA	10043
rs574009406	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	TOM1	GRCh38.p7	22:35298957	ACACACAGCCAGGAA[C/G]GCTGAAGAGATTAGA	10043
rs574013700	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35302241	GTTAAATAATGTCGG[A/G]GCCCCAACCCCAGAG	10043
rs574092117	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35341604	AGAGGTTGACTCCAC[C/T]ACCCAGTGGGCAGCA	10043
rs574154377	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334547	TGAGGAAGGGCACAC[A/G]GACCCTGCTTAGTAA	10043
rs574232558	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35312117	AAAAAATTAGGCGGG[C/T]GCCTGTAATCCCAGC	10043
rs574302602	snp	C/G/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35322679	CACAGGCTCACCAGT[C/G/T]GATTGACATCTCAGA	10043
rs574353393	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35303426	ACAAGATAGTCCTCT[A/G]AGAGTGTCTCGCACA	10043
rs574363717	snp	A/G	0.00279162	0.0372561	intron-variant, downstream-variant-500B	TOM1, MIR3909	GRCh38.p7	22:35336005	GGGGCAGGATGCTGA[A/G]AGGGTGGTGGGGCCC	10043
rs574402437	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35335556	CTTGCAGCCAGACAC[A/G]CCCATCCACAGAGGC	10043
rs574441888	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35317698	CAAGAATCTAGTGAC[A/G]ATGGGACAATGTGTA	10043
rs574450379	snp	C/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35305791	TATCCCCAGAGCCTT[C/G]CAAAGATGGAACTGG	10043
rs574533269	snp	A/G	1.68468e-05	0.00290226	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35330476	GTGTTCCTGCGCCAT[A/G]AACGGTAGCCCCAGC	10043
rs574649756	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35330108	TATGGCGAAACCCCG[C/T]CTCTACTAAAACTAC	10043
rs574685087	in-del	-/ACAAA			intron-variant	TOM1	GRCh38.p7	22:35301047	CGAGACCCCGTCTCT[-/ACAAA]AAAAAAAAAAAAAAA	10043
rs574686540	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35342401	TCCACTCTGGGGCCC[C/T]AGGAAACTGCATGTG	10043
rs574746599	in-del	-/CCA	0.0460142	0.144533	intron-variant	TOM1	GRCh38.p7	22:35343732	CACACACATCTACAC[-/CCA]CCACACCTACACACA	10043
rs574805023	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35328427	CTTGGTTCACATCGC[C/T]CACGTAATCCTGACC	10043
rs574836293	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35325373	TATGAAATCACCCCT[C/T]AGAGTTACAGATATT	10043
rs574950918	snp	C/T	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35318840	CCCTCCTTTCCCTCT[C/T]CAGTTCTCACTGGGA	10043
rs574965977	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334859	CCCTGCACTGTGTAC[C/T]GCATAGTAAGCCCTC	10043
rs574998452	snp	A/G	0.00398564	0.0444627	intron-variant	TOM1	GRCh38.p7	22:35343437	CACACACATATCTAC[A/G]CCCACCACACACACC	10043
rs575064344	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35336930	AGCTAAGCTTAGGAA[A/G]GGCAGATAGTTCTTT	10043
rs575247879	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35313818	GCTTGCCAGCCATAA[A/G]CAACTGCAAAGCCGC	10043
rs575297787	snp	A/G	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35332781	TTGGGACACTTTTGC[A/G]AGGGAAAGAGGAGCA	10043
rs575361494	snp	C/G	0.00279162	0.0372561	intron-variant	TOM1	GRCh38.p7	22:35332277	ATCTGGTAGCAGCTG[C/G]TACCCTCAGATATCC	10043
rs575372014	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35315641	CCCTCTGCCTCAGCC[A/G]CCTGGCATGTGTCCT	10043
rs575374029	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35309403	AATCCCAGCACTTTG[A/G]GAGGCCAAGACAGGC	10043
rs575385340	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35324797	TCAAGTGATCTACTC[A/G]TCTTGGCCTCCTAAA	10043
rs575423753	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35310503	AGGTTGCAGTGAGCC[A/G]AGATCGTGCCACTGC	10043
rs575447123	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35328033	GCCCAGGAGTCACCA[G/T]AATCCATGAGGAGAC	10043
rs575458930	snp	C/T	0	0	intron-variant	TOM1	GRCh38.p7	22:35320663	GAGGTCTTTTCTGAC[C/T]ACCCCCATCCTCACC	10043
rs575482713	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334066	GCCCAGCCACTTCCC[C/T]AGCAGAATCAATGGA	10043
rs575499736	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35320169	CTACCCAGGGTGGGC[A/C]CCCAGTTCAATGTGG	10043
rs575544343	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35326850	TCTAGGAGAGAGGGC[A/G]GAATCCCAGTCCTCT	10043
rs575548509	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	TOM1	GRCh38.p7	22:35297521	AGTGCAGTGGTGCAA[A/T]CTCTGCTCACTGCAA	10043
rs575609612	snp	C/G	0.00438332	0.0466095	intron-variant	TOM1	GRCh38.p7	22:35303726	TGGTCTTGAACTCCT[C/G]ACCTCAAGTGATCCA	10043
rs575738966	snp	G/T			intron-variant	TOM1	GRCh38.p7	22:35331557	AATGGGGGAGGAGCA[G/T]TTCCTCTAAAGAGTA	10043
rs575840745	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	TOM1	GRCh38.p7	22:35297930	GTGGCTCATGCCTGT[A/G]ACCCAGGGCTTTGGG	10043
rs575857676	in-del	-/T			intron-variant	TOM1	GRCh38.p7	22:35308291	TTTTTTTTTTTTTTC[-/T]TTTTTTTTTTGAGAC	10043
rs575887890	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35339606	TGTGGGCAGAGAGGA[A/G]TAAAAGAGCGGACCC	10043
rs576074477	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35316376	TGCACGTGGTTGACG[C/T]GTGAAGATAGCATCT	10043
rs576110046	snp	G/T	0.000137637	0.00829454	intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	TOM1	GRCh38.p7	22:35299881	TCGGTGGCGCTGGCG[G/T]TTGCTGTCAGCTGAT	10043
rs576129779	snp	G/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35311027	GGAGCACGAGTTGAG[G/T]TGGGGAGGAGCACAT	10043
rs576135702	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35322108	TCCCCTCAGACCCAG[C/T]AGGACTCCCAGCCTC	10043
rs576251975	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35312752	CATTGCAGACAGAAG[A/C]TCAGAGGCGTGAGAG	10043
rs576255096	snp	C/T	0.00279162	0.0372561	intron-variant	TOM1	GRCh38.p7	22:35340419	AGCACAGGAGGGACT[C/T]GACTTCCAATCTGAA	10043
rs576284235	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334589	GTATCCCCTAAGTCA[A/G]TCCAGCATGGCCTGG	10043
rs576286010	snp	G/T	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35346594	CCAGCACTCATCAAG[G/T]TCCCACTGGGCACCA	10043
rs576401439	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35305157	AGTGGACACTTAAGC[A/G]ATGTTGAGGAGACAC	10043
rs576520406	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35329984	AGGCCCGTGCATTAG[A/C]GATGGCCTCACTTGG	10043
rs576647635	snp	A/C	0.00438332	0.0466095	intron-variant	TOM1	GRCh38.p7	22:35318224	CCACACGGATCTGGA[A/C]GCCCAGCCTTGTGTG	10043
rs576649405	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334948	GTTGTTCCATAGCCA[C/T]CGTTAATTTCCAGAG	10043
rs576681161	snp	A/G	0.00530917	0.0512484	intron-variant	TOM1	GRCh38.p7	22:35331297	TTTTCTTTTTGCAGA[A/G]ACAGGGGTCTCACTG	10043
rs576681236	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35324862	GCCAAGAAGGTTTGA[A/G]GCTTAGTATGAGATT	10043
rs576691911	snp	A/G	5.16916e-05	0.00508361	synonymous-codon, nc-transcript-variant	TOM1	GRCh38.p7	22:35323869	CCCTCTGCCCGCCCC[A/G]CCCATACTCTCCGGT	10043
rs576698899	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	TOM1	GRCh38.p7	22:35347883	TCTGTTCCTTCTGGC[C/G]GGGCACCACAGCACT	10043
rs576700472	snp	G/T	0.00318978	0.0398085	intron-variant	TOM1	GRCh38.p7	22:35319656	CCAGGGAATGATTCT[G/T]ATTCCCTTGTGTCTA	10043
rs576703049	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35313406	TCTCTGATCCTGCCC[A/G]TGGTGTGGCGTGTCT	10043
rs576716262	in-del	-/C	0.00478085	0.0486577	intron-variant	TOM1	GRCh38.p7	22:35311227	TGCCGTAGTTGTCCA[-/C]CCGCGGAGCAGTCCC	10043
rs576744483	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	TOM1, MIR3909	GRCh38.p7	22:35336165	GCACCTTCTCAGGCC[A/G]TTGGTTCTCCTGCAG	10043
rs576766745	snp	A/T	6.58892e-05	0.00573936	synonymous-codon, nc-transcript-variant	TOM1	GRCh38.p7	22:35332996	GTTTGAACGGTTCCG[A/T]ACAGGCCAGACCACC	10043
rs576799030	snp	A/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35300897	TGGCCAGTGCCATAT[A/T]AAAAAAAACAGTTGT	10043
rs576814105	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35340595	CTACAAAATATTTAA[A/G]AATTATCCGGGCATG	10043
rs576831561	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35342513	AGACCATCTGACAGC[C/T]GCCTGCCCTGCTATC	10043
rs576876443	snp	C/T	0.00478085	0.0486577	intron-variant	TOM1	GRCh38.p7	22:35341732	TCCTGGCTCCCACAC[C/T]ACCTTGCAGCCCGCC	10043
rs577013667	snp	A/G	0.00159617	0.0282053	downstream-variant-500B	TOM1	GRCh38.p7	22:35348345	GCACAGGCCACAGGA[A/G]GATGCTGGCCTTCCG	10043
rs577089246	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35344475	AGCTCCTCTGTGCCC[A/G]GTTCCTGCTCTTGAG	10043
rs577110990	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	TOM1, MIR6069	GRCh38.p7	22:35336704	GTGGCCCAGGTGCAG[C/T]CCCTGCCCACCAGCC	10043
rs577124351	snp	A/G/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35344101	CCAAAGTGGCAGCAG[A/G/T]CCTCCTGACCCGAAA	10043
rs577190797	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35314249	AACAGCTGTCTTGTA[C/T]TGGAATTGCTCAGAT	10043
rs577313026	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35319361	CAGCAGTGATCAAAG[A/G]CAGGCATGACCCTTG	10043
rs577356764	snp	C/G			intron-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35337223	TTTCAGCCACTGCAC[C/G]TGGCCCAGATAGTTG	10043
rs577401788	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35339989	GTTCCTTGACTGTGT[A/G]TTGAGTGACAGCCAC	10043
rs577550842	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35302996	TCTCAAGCCTGCCGA[C/T]TCCCATGCCCTTGTT	10043
rs577611473	snp	C/T	0.00358779	0.0422022	intron-variant	TOM1	GRCh38.p7	22:35302469	GCCTCCCAAGGTAGC[C/T]GGGATTACAGGCACG	10043
rs577690650	snp	C/T	0.00279162	0.0372561	intron-variant	TOM1	GRCh38.p7	22:35313228	GGCAGGTACCTGTAA[C/T]CCCAGCTACTCGGGA	10043
rs577710698	snp	C/G	0.000798403	0.0199641	intron-variant	TOM1	GRCh38.p7	22:35332863	CCAGACGTGTCATCA[C/G]CCTGATCATAACCCA	10043
rs577710799	snp	A/G	0.00318978	0.0398085	intron-variant	TOM1	GRCh38.p7	22:35304356	CCAAGGGCAGCACCC[A/G]TAGCTGAGAGGATTC	10043
rs577715174	snp	C/G	0.00279162	0.0372561	upstream-variant-2KB	TOM1	GRCh38.p7	22:35297587	CAGCCTCCCGAGTAG[C/G]TGGGACTACAGGCGC	10043
rs577717106	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35343428	CACACACCACACACA[C/T]ATATCTACACCCACC	10043
rs577720219	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35320731	TCTTTGGATCTCCCC[A/G]CAAGGTGGGGAGGAG	10043
rs577730267	snp	A/G	0.000481044	0.0155013	synonymous-codon, nc-transcript-variant	TOM1	GRCh38.p7	22:35327357	GCTGGTGCCCACCCA[A/G]GCCGAGCCCGCAGAC	10043
rs577787561	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35310251	AGATTAAGGAGGGAC[A/G]TGGTACTTTTTAAAA	10043
rs577823721	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35322490	GGCGGCCAGACACAC[A/G]TGGGCCTCCTAGCCG	10043
rs577872880	snp	C/T	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35328527	TAAGTAGCAGAGCTG[C/T]GATTTGAACCCGGGG	10043
rs577992337	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35319097	ACTCATGAGAGTGAG[A/G]GTGAGGGAAGGAGTG	10043
rs578024602	snp	A/G	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35339741	AACCCCGTCTCTACT[A/G]AAAATACAAAAAATT	10043
rs578031743	snp	A/C	0.000399281	0.0141238	intron-variant	TOM1	GRCh38.p7	22:35321465	GTACAGTGGCGTAAT[A/C]TCGGCTCACTGCAAC	10043
rs578039574	snp	C/T	0.0023933	0.0345097	intron-variant	TOM1	GRCh38.p7	22:35338915	CCTTCCTCGTTTGGC[C/T]GTCAGGTCGGTTCTT	10043
rs578074630	snp	C/G	0.00199481	0.0315187	upstream-variant-2KB	TOM1	GRCh38.p7	22:35298455	TTTTTTTTTTTAAGA[C/G]ACAGCCTTACTCTGT	10043
rs578123280	snp	A/C/T	0.000192042	0.00979727	synonymous-codon, nc-transcript-variant	TOM1	GRCh38.p7	22:35323881	CCCGCCCATACTCTC[A/C/T]GGTGACACGCCCATA	10043
rs578218594	snp	C/T	4.94776e-05	0.00497357	missense, nc-transcript-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334427	TGACACGGGGCAGCT[C/T]ACTGGCTGACCAACG	10043
rs745422726	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35339192	AAAAATTAGCTGGGC[A/G]TGGTGGCACATGCCT	10043
rs745475934	snp	C/G/T	4.94534e-05	0.00497239	missense, nc-transcript-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334409	AGTTTGACATGTTTG[C/G/T]GCTGACACGGGGCAG	10043
rs745477880	snp	C/T	1.70194e-05	0.00291709	intron-variant	TOM1	GRCh38.p7	22:35323751	AGCCCTCACTGATCC[C/T]GTTTTCCTCCCACTA	10043
rs745525698	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35328071	TTCGTGTAACTGTTC[A/G]AGTTCCTACTGCTCG	10043
rs745541221	in-del	-/GC			intron-variant	TOM1	GRCh38.p7	22:35318449	GAAGCTGAACCGTGA[-/GC]CTGAACAGCACTGGC	10043
rs745568024	in-del	-/CTC	1.79774e-05	0.00299806	intron-variant	TOM1	GRCh38.p7	22:35322985	TTCTGAGCACCTCCT[-/CTC]CTCTGACCAAGGTGC	10043
rs745578352	snp	C/T	1.92888e-05	0.00310549	intron-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35321748	TTCTCAAAGTGACTC[C/T]GCTGCTGGAGGTCCA	10043
rs745648240	snp	A/T			intron-variant	TOM1	GRCh38.p7	22:35345596	GGGCCCAGTGGTGGG[A/T]CCGGGCAGCTAGGCA	10043
rs745719013	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35332294	ACCCTCAGATATCCA[C/T]AGTCATTAGGCTTAA	10043
rs745745307	snp	C/T	3.31884e-05	0.00407346	synonymous-codon, nc-transcript-variant	TOM1	GRCh38.p7	22:35333466	TGACCCAGCAGCCAC[C/T]GGCAACCTCTCATCC	10043
rs745751433	snp	C/T	1.65422e-05	0.0028759	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35330434	CTGACAGAGGAGCTG[C/T]TCATCGTCAATGACA	10043
rs745766211	snp	C/G			intron-variant	TOM1	GRCh38.p7	22:35319478	GCTCCCAGCAGAGTA[C/G]CGGACATCATGGGCC	10043
rs745796312	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35320628	ATCTTTCAAGGCCCA[A/G]CTACAAGACCACCCC	10043
rs745868375	snp	C/T	0.000196676	0.00991461	intron-variant	TOM1	GRCh38.p7	22:35331285	TTCTTTTTTTTTTTT[C/T]CTTTTTGCAGAGACA	10043
rs745946515	snp	A/C	0.000116809	0.00764138	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35338728	GGTAAAATACGAAGC[A/C]CCCCAAGCAACAGAC	10043
rs746013745	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35325265	ACTTTCCCAATAAGC[A/G]TCCCCACTGCCCACT	10043
rs746066718	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35314028	TGAATTACTTCTGTG[A/G]TGAAGAACAAAAACA	10043
rs746193519	in-del	-/CACACCTACACCTACC			intron-variant	TOM1	GRCh38.p7	22:35343787	CACCTACACACACCA[-/CACACCTACACCTACC]CACACCTACACCTAC	10043
rs746242930	snp	C/G	3.34924e-05	0.00409208	intron-variant	TOM1	GRCh38.p7	22:35347038	GGGCCTACCCTCACC[C/G]TCTCCCCTTCCTCTA	10043
rs746244306	snp	C/T			downstream-variant-500B	TOM1	GRCh38.p7	22:35348174	GCAGGCTCCAGCCAC[C/T]GCCCCTGCCCGGAGG	10043
rs746244494	in-del	-/TG			intron-variant	TOM1	GRCh38.p7	22:35308216	TCGCTCTTTCTCCTG[-/TG]TGTGTGTGTGTGTGT	10043
rs746286549	snp	C/T	3.29538e-05	0.00405904	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35317947	CTGCGACATCATCAA[C/T]GAGACGGAGGAAGGG	10043
rs746325920	snp	C/T	3.29663e-05	0.00405981	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35327326	ACGTGAGGGTGATGT[C/T]GGAGATGCTGACGGA	10043
rs746336831	snp	A/G			intron-variant, nc-transcript-variant	TOM1, MIR3909	GRCh38.p7	22:35335683	GGGAGCAGGCTCCGG[A/G]GGACAGGGAAAAGCA	10043
rs746392683	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35310024	GCTCCACATGGTAGG[A/G]TTAATAAAAATTTCA	10043
rs746398937	snp	A/C	1.92077e-05	0.00309895	intron-variant	TOM1	GRCh38.p7	22:35322960	ACAGGAGGAGCCACG[A/C]GGGTGGGGGTTCTGA	10043
rs746400046	snp	A/G			intron-variant, nc-transcript-variant	TOM1, MIR6069	GRCh38.p7	22:35336765	ACCCTCCTGCACTGG[A/G]CAGGGGGCAGCAGGC	10043
rs746563663	snp	A/C			intron-variant	TOM1	GRCh38.p7	22:35342154	TCAAAAAAAAAGAAA[A/C]AGAATCAAGTGCCAA	10043
rs746563723	snp	G/T	1.66114e-05	0.00288192	synonymous-codon, nc-transcript-variant	TOM1	GRCh38.p7	22:35347140	TGAGGGGCCCCCGGG[G/T]CCCCCATCTGGCCCA	10043
rs746632701	snp	C/T	1.66021e-05	0.0028811	synonymous-codon, nc-transcript-variant	TOM1	GRCh38.p7	22:35333434	GAGCCGGCAGCTGAC[C/T]TGATCGACATGGGCC	10043
rs746677596	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35316809	TAAAAAGAACCACCA[C/T]CACTTGCTGAGTGTT	10043
rs746687192	snp	A/G	7.17502e-05	0.00598915	intron-variant	TOM1	GRCh38.p7	22:35333546	ACATTATGGTACTGT[A/G]GGCACCCCTGCAGAT	10043
rs746720662	snp	C/T	3.2962e-05	0.00405954	synonymous-codon, intron-variant, nc-transcript-variant	TOM1	GRCh38.p7	22:35323615	CATGCTGTCACCCAT[C/T]CACACACCCCAGAGG	10043
rs746725954	snp	A/G			intron-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35338419	GAGCCTACGGGCACT[A/G]GAGCTATTTATCAGT	10043
rs746801273	in-del	-/C			intron-variant	TOM1	GRCh38.p7	22:35328663	ATGTTGAAAGGCACC[-/C]GCCCTGTCCCCGTGC	10043
rs746807235	snp	C/T	3.30551e-05	0.00406528	synonymous-codon, nc-transcript-variant	TOM1	GRCh38.p7	22:35330406	GCTCATCCCTCAGAT[C/T]GCCAATGAGCAGCTG	10043
rs746873196	in-del	-/GT			intron-variant	TOM1	GRCh38.p7	22:35303016	ATGCCCTTGTTGATA[-/GT]AGAGCTGTAGAGCCA	10043
rs746887313	snp	A/C	1.6495e-05	0.0028718	intron-variant	TOM1	GRCh38.p7	22:35345706	AGGGCACTGCCTTAC[A/C]CTCTGCCCTTCCTTC	10043
rs746917163	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35310582	TCAGAGGATTGCAAG[C/T]TGGAAGAAGGATTAG	10043
rs746926122	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35311250	GCAGTCCCGTGGGAA[A/G]GCCAGGGCAGCTGGA	10043
rs746972793	snp	C/T			intron-variant, utr-variant-5-prime, nc-transcript-variant	TOM1	GRCh38.p7	22:35299915	CGGGGTTGGTGGCAG[C/T]GGCGGTAGCAGCAAT	10043
rs747023539	snp	C/T	1.64833e-05	0.00287078	synonymous-codon, nc-transcript-variant	TOM1	GRCh38.p7	22:35345760	CCTCATGGAGGACAT[C/T]GAGCAGTGGCTGTCC	10043
rs747054394	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35322060	CCCCATCTGTCTGTC[C/T]TGTGGCAGGACTACG	10043
rs747095460	snp	A/G	6.27766e-05	0.00560217	intron-variant, utr-variant-5-prime, nc-transcript-variant	TOM1	GRCh38.p7	22:35299926	GCAGCGGCGGTAGCA[A/G]CAATGGACTTTCTCC	10043
rs747164647	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35345108	ACAGCCCATGTCTTT[A/G]TGGCCGAAAGTGAAA	10043
rs747180894	snp	C/T	1.65622e-05	0.00287764	missense, nc-transcript-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35323116	GTGTGCTGGTGAGGA[C/T]CATCCTGCCCAAGAA	10043
rs747262658	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35305186	ACCAGGCTGGGAGGC[A/G]GGACACCTGGTTCCA	10043
rs747268467	snp	G/T	1.68496e-05	0.0029025	intron-variant	TOM1	GRCh38.p7	22:35323205	ACAGGGCAGGGCACG[G/T]CCAGGAAGAGCTGTC	10043
rs747330668	snp	C/T	1.64904e-05	0.00287139	synonymous-codon, nc-transcript-variant, intron-variant	TOM1	GRCh38.p7	22:35322031	CGAGGTGATGCTGGC[C/T]CTCACAGTGAGTGCC	10043
rs747427560	snp	A/C			intron-variant, downstream-variant-500B	TOM1, MIR3909	GRCh38.p7	22:35335840	CATGCAACTCTGCGG[A/C]GGGTACTCAGAGCTG	10043
rs747507868	snp	G/T			intron-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35337872	GGCGAGAATAACAGG[G/T]CTCTTTCCCTGCAAC	10043
rs747582416	in-del	-/TT			intron-variant	TOM1	GRCh38.p7	22:35302332	TCTTTTTCTTTTTCT[-/TT]TTTTTTTTTTTTTTT	10043
rs747596395	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35313026	GGCTCCAGGCTGCTT[C/T]CCAGAAGGCTGGTGT	10043
rs747645107	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35329117	TACACCACCATGCCC[A/G]GCTAATTTTTGTATT	10043
rs747651946	snp	G/T			intron-variant	TOM1	GRCh38.p7	22:35316944	CTCGGCATCGGTCCC[G/T]TCTGTGGGTGCCTCA	10043
rs747699607	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35330295	AAAAAAAAAAGAGAC[A/G]GCCTCACTCTGAGTC	10043
rs747775077	snp	A/G	1.94015e-05	0.00311454	intron-variant	TOM1	GRCh38.p7	22:35322954	TGGGACACAGGAGGA[A/G]CCACGAGGGTGGGGG	10043
rs747791297	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35318445	AAGTGAAGCTGAACC[A/G]TGAGCCTGAACAGCA	10043
rs747810511	snp	G/T	1.67309e-05	0.00289226	intron-variant	TOM1	GRCh38.p7	22:35347009	CCTCTCCTTTCCCCA[G/T]GGCTCTGGCCTCAGG	10043
rs747889483	snp	A/G	1.64727e-05	0.00286986	synonymous-codon, nc-transcript-variant	TOM1	GRCh38.p7	22:35333005	GTTCCGAACAGGCCA[A/G]ACCACCAAGGTAAAA	10043
rs747939957	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35324073	TTGAGCGATGAGACT[C/T]AGAGAGGTCCATTCA	10043
rs748047226	snp	C/T	1.65765e-05	0.00287888	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35323069	CGGGCACCGCTTCCA[C/T]GTGCTGGTGGCCAGC	10043
rs748048887	snp	C/T	1.64792e-05	0.00287042	missense, intron-variant, nc-transcript-variant	TOM1	GRCh38.p7	22:35323605	CTGACCTGGACATGC[C/T]GTCACCCATCCACAC	10043
rs748068985	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35300794	TCACCTGTAGTTGGC[A/G]GGCAATAATGGTCCC	10043
rs748096047	snp	A/G			intron-variant, upstream-variant-2KB	TOM1	GRCh38.p7	22:35299764	CCCTCCGCCTCGGGG[A/G]CGGGACCCTGGCGTC	10043
rs748134719	snp	A/G	1.64781e-05	0.00287033	missense, nc-transcript-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35317948	TGCGACATCATCAAC[A/G]AGACGGAGGAAGGGT	10043
rs748222112	snp	C/T			utr-variant-3-prime, nc-transcript-variant	TOM1	GRCh38.p7	22:35347844	GCCCCACTGCCCCTC[C/T]GCTGCCTTGCCCTCC	10043
rs748253816	snp	C/T	8.27945e-05	0.00643354	missense, nc-transcript-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35323110	TGGAGAGTGTGCTGG[C/T]GAGGACCATCCTGCC	10043
rs748271310	snp	C/T	6.8653e-05	0.00585848	intron-variant	TOM1	GRCh38.p7	22:35330318	TCTGAGTCATGTGAC[C/T]GTGGTTGCCTCACTT	10043
rs748275387	snp	C/T			intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334902	AGTTTCCTGATAAAT[C/T]CTCAGGGACTTTCAA	10043
rs748319311	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35305315	AGGATTGGTAAGGAA[C/T]GACAGAGGTCATATA	10043
rs748360916	snp	G/T	1.66538e-05	0.00288559	stop-gained, nc-transcript-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35323034	GCCCTCCAGGTCTTA[G/T]AAACCTGTGTCAAGA	10043
rs748386637	snp	C/T	8.33132e-05	0.00645365	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35347162	TCTGGCCCAGCGCCC[C/T]GGAAGAAGACCCAGG	10043
rs748403817	snp	G/T			upstream-variant-2KB	TOM1	GRCh38.p7	22:35297686	GTGTTAGCCAGGATG[G/T]TCTTGATCTCCTGAC	10043
rs748506969	snp	C/G			intron-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35338521	CCCTAACCTCTCCAG[C/G]CTTTGCTGCTGTCTG	10043
rs748511616	snp	A/T	1.73664e-05	0.00294667	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35323877	CCGCCCCGCCCATAC[A/T]CTCCGGTGACACGCC	10043
rs748557304	snp	G/T			intron-variant	TOM1	GRCh38.p7	22:35315209	GCAGGGGCAGTGGCA[G/T]AGGGGATGGTGTGAT	10043
rs748621118	snp	C/G			intron-variant	TOM1	GRCh38.p7	22:35327908	GGTATTCCCACGGCC[C/G]CAGCCCAGATTGGGG	10043
rs748631277	in-del	-/T	1.64804e-05	0.00287053	intron-variant	TOM1	GRCh38.p7	22:35327245	GAACCCTGGCTTCTC[-/T]CACCACGATCAACTG	10043
rs748657264	snp	A/G	1.64871e-05	0.00287111	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334413	TGACATGTTTGCGCT[A/G]ACACGGGGCAGCTCA	10043
rs748684506	in-del	-/G	1.66412e-05	0.00288449	frameshift-variant, nc-transcript-variant	TOM1	GRCh38.p7	22:35346969	GGGGTCACCAGCGAA[-/G]GTAGTAGTCCCCGCC	10043
rs748686231	snp	C/G			intron-variant, downstream-variant-500B	TOM1, MIR6069	GRCh38.p7	22:35336425	CCAGCTCTGCCCTGG[C/G]TGGCAGGGAAACCAG	10043
rs748813088	snp	C/T	0.000197025	0.00992339	intron-variant	TOM1	GRCh38.p7	22:35331318	GGTCTCACTGTGTTG[C/T]CCAGGCTAGTCTCAA	10043
rs748815065	in-del	-/G	1.65142e-05	0.00287347	frameshift-variant, intron-variant, nc-transcript-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35323507	CAGTCCTGGGCTGAC[-/G]GCGTTCCGCAGCTCG	10043
rs748865489	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35307549	CCCGGCTGTGTCCCC[C/T]AGGTCTCCTCCTCAA	10043
rs748914491	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35308853	GGTTGCGGAAGCAAT[A/G]CCCTCTGTAAGGTAT	10043
rs749025244	snp	A/G	1.64779e-05	0.00287031	missense, intron-variant, nc-transcript-variant	TOM1	GRCh38.p7	22:35323592	GAGTTCCCCATGACT[A/G]ACCTGGACATGCTGT	10043
rs749029529	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35342575	CTTGTGGAGAGAGTT[A/G]AGAAGCTTTGTTTAG	10043
rs749080184	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35321510	TTCAAGCGATTCTCC[C/T]GCCTCAACCTCCCAA	10043
rs749153525	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35301189	CCCTGATGGCGCCAC[C/T]GTACTCCAGCCTGGA	10043
rs749192174	snp	A/G	4.94173e-05	0.00497053	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35332995	GGTTTGAACGGTTCC[A/G]AACAGGCCAGACCAC	10043
rs749201037	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35331856	TCGCACCACTGCACT[C/T]CAGCCTAGGCGACAG	10043
rs749206244	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35302980	CAGGAGTACCATCTC[C/T]TCTCAAGCCTGCCGA	10043
rs749213029	snp	C/T	3.31301e-05	0.00406989	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35330380	CGAGCCATGCAGCAG[C/T]GGGTCCTGGAGCTCA	10043
rs749240422	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35318489	GGCGTTTCTGGTGTT[A/G]GGGTCACGGTATCGT	10043
rs749288558	snp	C/T	1.65012e-05	0.00287234	missense, intron-variant, nc-transcript-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35323514	TGGGCTGACGCGTTC[C/T]GCAGCTCGCCCGATC	10043
rs749378574	snp	A/G	1.89406e-05	0.00307733	intron-variant	TOM1	GRCh38.p7	22:35322967	GAGCCACGAGGGTGG[A/G]GGTTCTGAGCACCTC	10043
rs749385763	snp	A/C	1.72095e-05	0.00293333	intron-variant	TOM1	GRCh38.p7	22:35330311	GCCTCACTCTGAGTC[A/C]TGTGACTGTGGTTGC	10043
rs749413768	snp	C/G	0.00254777	0.0356004	intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35335607	GCCATACTGGAGAAC[C/G]CTGGCGCCTGCCCTG	10043
rs749418614	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35323278	GTTTGTCCCAGGCTC[C/T]GCTTCTCATTTCGGG	10043
rs749433167	snp	A/G	4.84015e-05	0.00491919	missense, nc-transcript-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35338741	GCCCCCCAAGCAACA[A/G]ACGGCCTGGCTGGAG	10043
rs749473852	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35312693	TGCATGCTGAGTGCC[A/G]GATGAGCATGTGAAC	10043
rs749523049	snp	A/G	1.65119e-05	0.00287327	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35327346	ATGCTGACGGAGCTG[A/G]TGCCCACCCAGGCCG	10043
rs749575881	snp	A/G	3.40675e-05	0.00412705	intron-variant	TOM1	GRCh38.p7	22:35338832	GGGGCCCTCCTGAAG[A/G]AGGTGAGGGAATGCT	10043
rs749657188	snp	A/G	1.6656e-05	0.00288578	intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334284	CAGCAGCTCACACAC[A/G]AGCTTGTGGATGGGT	10043
rs749771091	snp	A/G	5.00588e-05	0.00500269	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35347079	AATTCCTGGAAGAAC[A/G]GGCCAAAGCCGCGGA	10043
rs749828374	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35306402	TCTGTTTCCTGATCC[A/G]TAAGTACAGGACCCA	10043
rs749926182	snp	A/G	0.000132582	0.00814085	intron-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35338689	TAAGGGCAGCATCCA[A/G]TGGCTTGGTGGTCTC	10043
rs750007427	snp	G/T			intron-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35321742	CATCTTTTCTCAAAG[G/T]GACTCTGCTGCTGGA	10043
rs750022778	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35322686	TCACCAGTCGATTGA[C/T]ATCTCAGATGCTCCT	10043
rs750027686	snp	A/G	1.65935e-05	0.00288036	intron-variant	TOM1	GRCh38.p7	22:35323471	GAGCTGTGGTTACCG[A/G]CTGTGTCCCCTTGTC	10043
rs750044798	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35311216	CCTTCAGGTCCATGC[C/T]GTAGTTGTCCACCGC	10043
rs750077304	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35311807	CAAATGGAGGTCCTC[C/T]GAGCATCCTGCACAG	10043
rs750107231	in-del	-/GGCTGGCT			utr-variant-3-prime, nc-transcript-variant	TOM1	GRCh38.p7	22:35347489	GGAGGCCCCAGGACA[-/GGCTGGCT]GGCTGGCTGGCTGGC	10043
rs750116536	in-del	-/GAA	1.6473e-05	0.00286988	intron-variant	TOM1	GRCh38.p7	22:35333059	AGGCCCTGTTCATGG[-/GAA]GAAGGAGTGCCATTC	10043
rs750118972	snp	C/T	4.95593e-05	0.00497767	intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334474	TGGCCCTGCCCTGGT[C/T]CCCTGCAGTTCGGGT	10043
rs750123288	snp	A/G	7.9255e-05	0.00629454	intron-variant	TOM1	GRCh38.p7	22:35299994	CGGTGAGTCCCTGGA[A/G]CCCCCCACAGCTCCG	10043
rs750284827	snp	A/T			intron-variant	TOM1	GRCh38.p7	22:35346165	CACCACCCTGTTTAC[A/T]GATCAGAAGACCGAT	10043
rs750309786	snp	A/G	1.6476e-05	0.00287014	synonymous-codon, nc-transcript-variant, intron-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35321998	AAAGAAGAGAATCGT[A/G]GGGAATAAGAACTTC	10043
rs750391365	snp	A/G	0.000263809	0.0114819	missense, nc-transcript-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334418	TGTTTGCGCTGACAC[A/G]GGGCAGCTCACTGGC	10043
rs750482002	snp	C/T	1.64743e-05	0.00287	utr-variant-5-prime, synonymous-codon, nc-transcript-variant	TOM1	GRCh38.p7	22:35317905	TGGCTCCCTGCAGAG[C/T]GAGGACTGGGCCCTC	10043
rs750536713	snp	A/G			intron-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35337726	CAGCCCCGCTTCACT[A/G]GCGTGTCAGGTGGCC	10043
rs750609493	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35340324	TCTATGGGTATATAG[C/T]AGGGACCAGAGGACC	10043
rs750646372	snp	C/G	1.66352e-05	0.00288398	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35333484	CAACCTCTCATCCCA[C/G]CTGGCAGGAATGAGT	10043
rs750649369	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35327505	ACTCCTTGGTCACAG[C/T]TGGGGACATGTTACC	10043
rs750649492	snp	G/T			intron-variant	TOM1	GRCh38.p7	22:35314774	CTGCTGAGAGATGCG[G/T]ATGGCACAGAAGCCT	10043
rs750692958	snp	C/T	1.64795e-05	0.00287045	synonymous-codon, intron-variant, nc-transcript-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35323585	AGGCCTGGAGTTCCC[C/T]ATGACTGACCTGGAC	10043
rs750797707	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35340891	TCCCAAGTCAGAACA[A/G]GGCAAGGTGGAGGAC	10043
rs750848373	snp	A/G	1.6729e-05	0.00289209	intron-variant	TOM1	GRCh38.p7	22:35338801	GCGGTAAGCAGAGGG[A/G]CCATCCTGCCACCCT	10043
rs750921746	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35319086	TCTTGCCAAGGACTC[A/G]TGAGAGTGAGGGTGA	10043
rs750980581	snp	C/T	1.64846e-05	0.0028709	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35345729	CTTCCTTCCAGATCC[C/T]AGTCACCCAGGCCTG	10043
rs751001604	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35308230	TGTGTGTGTGTGTGT[A/G]TCTGTCTCTCTCTCT	10043
rs751007796	snp	C/G	3.45728e-05	0.00415755	intron-variant	TOM1	GRCh38.p7	22:35330296	AAAAAAAAAGAGACG[C/G]CCTCACTCTGAGTCA	10043
rs751021039	snp	A/C/T	3.50977e-05	0.00418902	utr-variant-3-prime, nc-transcript-variant	TOM1	GRCh38.p7	22:35347230	GGGTCTGGCACCCTG[A/C/T]AGCCCAGGTCCCCAC	10043
rs751050907	snp	C/T	1.68906e-05	0.00290603	intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	TOM1	GRCh38.p7	22:35299886	GGCGCTGGCGGTTGC[C/T]GTCAGCTGATTCCCG	10043
rs751075456	snp	C/T	6.59207e-05	0.00574073	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334374	GCAGTCTCTGGAGGC[C/T]TCTGGTCGACTGGAA	10043
rs751079811	snp	C/G			utr-variant-3-prime, nc-transcript-variant	TOM1	GRCh38.p7	22:35347321	GGTGGCTTGTTACCC[C/G]CTTTTCCTCCTCTTT	10043
rs751123999	snp	C/T			intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	TOM1	GRCh38.p7	22:35299866	GCGTCACGTGACGGG[C/T]CGGTGGCGCTGGCGG	10043
rs751143698	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35313630	TCTATGAGTTAGGTC[A/G]GGCCAGACTCGTCCC	10043
rs751186163	snp	C/G			intron-variant	TOM1	GRCh38.p7	22:35330210	AATGGCATGAACCCA[C/G]GACACAGCTTGCAGT	10043
rs751194351	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35302576	TGAACAGGTGACCCA[C/T]CCACCTCAGCCTCCC	10043
rs751194991	snp	A/G	1.65696e-05	0.00287828	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35323072	GCACCGCTTCCACGT[A/G]CTGGTGGCCAGCCAG	10043
rs751196335	snp	C/G			intron-variant	TOM1	GRCh38.p7	22:35300505	AGCCCGCGGCCAGGC[C/G]TCACAGACCCGGGTC	10043
rs751226226	snp	A/C			intron-variant	TOM1	GRCh38.p7	22:35344439	CTGTTTCCGGGTTGG[A/C]CCGGCCAGCCCAGCT	10043
rs751229262	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35306222	CAGACTGAATTTGGC[A/G]TATGGGTTCATAGTT	10043
rs751280686	snp	A/G	1.66299e-05	0.00288352	missense, nc-transcript-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35323160	ATCGTGCATGACAAA[A/G]TGCTCAACCTCATCC	10043
rs751292572	snp	A/G	1.64749e-05	0.00287005	synonymous-codon, nc-transcript-variant, intron-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35321977	CAAAGATGCCCTCCG[A/G]GCAGTAAAGAAGAGA	10043
rs751298014	snp	A/T			intron-variant	TOM1	GRCh38.p7	22:35306031	ACAAAAGCAGCTACA[A/T]AGGCCATAGGTAAAT	10043
rs751353748	snp	C/G			utr-variant-3-prime, nc-transcript-variant	TOM1	GRCh38.p7	22:35347445	GCCTCCTTTCCCACC[C/G]CAGCTGACCATGAGA	10043
rs751364020	in-del	-/ACACACACAC			intron-variant	TOM1	GRCh38.p7	22:35332586	CTGAAGAGAGCACTA[-/ACACACACAC]ACACACACACATACA	10043
rs751440861	snp	C/T	1.65094e-05	0.00287305	intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334463	AGTGAGTGGCCTGGC[C/T]CTGCCCTGGTCCCCT	10043
rs751465929	snp	A/T			intron-variant	TOM1	GRCh38.p7	22:35329558	CCAAAGCTAAAAGTT[A/T]GTTTAAAAAGACAAA	10043
rs751496038	snp	A/T			intron-variant	TOM1	GRCh38.p7	22:35307065	CCCTCAGTGTCTCCT[A/T]ATTAGCTTGAGGCCA	10043
rs751525601	snp	A/G			upstream-variant-2KB	TOM1	GRCh38.p7	22:35298803	GATTTAAAAACCACA[A/G]ACATCACAATAAGTA	10043
rs751548792	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35322788	CACTGACGCCAGTCA[A/G]GGAAGGAAGTCCAGC	10043
rs751623243	snp	C/T	4.96783e-05	0.00498364	intron-variant	TOM1	GRCh38.p7	22:35323487	CTGTGTCCCCTTGTC[C/T]CCTCTCAGTCCTGGG	10043
rs751638973	in-del	-/CACAC			intron-variant	TOM1	GRCh38.p7	22:35343636	ACACCCACACCTACA[-/CACAC]CACACCTATACTCAT	10043
rs751754859	snp	A/G	5.00714e-05	0.00500332	intron-variant	TOM1	GRCh38.p7	22:35346920	GCCTCCTTTCCTTCT[A/G]CCTTCCCAGGGTAAT	10043
rs751762217	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35315707	GGGTAGAACTGAAGT[C/T]GGGCCAATTGCAAAA	10043
rs751787373	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35328492	GAGATCAGATAACAC[A/G]TCCAGGGTTATATGG	10043
rs751817721	snp	C/T	1.6473e-05	0.00286988	intron-variant	TOM1	GRCh38.p7	22:35332973	CTCGTGTCTTTTCTG[C/T]CTTGTAGGTTTGAAC	10043
rs751867925	snp	A/C			intron-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35337338	TGTCTTAGAGACAGC[A/C]ACAAGCACCTCCAGA	10043
rs751968341	snp	A/C			intron-variant	TOM1	GRCh38.p7	22:35300991	CCAAGGCGGGCAGAT[A/C]GCTTGAGCCCAGGAG	10043
rs751982967	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35320266	TGAGGCTTCACCTCA[C/T]GGATGTGGAGGTCAG	10043
rs751999436	snp	A/G	1.64787e-05	0.00287038	synonymous-codon, intron-variant, nc-transcript-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35323564	CTATGAGGACCTGCG[A/G]AGGAAAGGCCTGGAG	10043
rs752017475	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35340662	TGAGGTGGGAGGATC[A/G]CTTGAGCACAGGAGG	10043
rs752027351	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35311109	GTGATGGGGTGGCTG[C/T]GGGCGATCAGCTGAG	10043
rs752077217	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35310151	TGGCTGGCCTATATC[C/T]AGAGGGGTCGGTCAG	10043
rs752119958	snp	C/G			upstream-variant-2KB	TOM1	GRCh38.p7	22:35298927	ATCTAGTGTGTAGGT[C/G]TCAGCAGACACACCA	10043
rs752134095	snp	C/T	1.64754e-05	0.00287009	utr-variant-5-prime, missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35317895	AAGCCACAGATGGCT[C/T]CCTGCAGAGCGAGGA	10043
rs752135465	snp	G/T			upstream-variant-2KB	TOM1	GRCh38.p7	22:35297460	TGCATGGAGTTGTTT[G/T]TCTTTTTTTTTTTGA	10043
rs752159736	snp	A/G	1.65982e-05	0.00288077	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35338716	TCTCTCTTTCAGGGT[A/G]AAATACGAAGCCCCC	10043
rs752188110	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35341188	CCCTTAGGGTATGTT[A/G]TTATCCCGTTTTACA	10043
rs752194520	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35314520	ATTTATCAATGTCCC[C/T]GCTTCCCTTTAAAAG	10043
rs752194840	snp	A/C			intron-variant	TOM1	GRCh38.p7	22:35302883	TAGATAAAGAGGCGG[A/C]GGAAGTACTGCTCCC	10043
rs752240918	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35344544	AGGCGATGGGGATAG[C/T]GGAGCGGGAGACGGA	10043
rs752294350	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35331701	CCAGCCAGGCCAACA[C/T]GGTGAAACCCCGTCT	10043
rs752347385	snp	C/G			intron-variant	TOM1	GRCh38.p7	22:35332921	GAAAAGCTCTGCCTG[C/G]CCGTGTGTGGGGGCC	10043
rs752422737	snp	C/T	6.67134e-05	0.00577514	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35330360	AGGAGCTCAACCGCA[C/T]GTGCCGAGCCATGCA	10043
rs752485513	snp	C/T	1.73297e-05	0.00294356	utr-variant-3-prime, nc-transcript-variant	TOM1	GRCh38.p7	22:35347219	TTATGAGTGTGGGGT[C/T]TGGCACCCTGCAGCC	10043
rs752535105	snp	A/G			synonymous-codon, nc-transcript-variant	TOM1	GRCh38.p7	22:35327279	GTTTCAGATTGGGAA[A/G]CTGCGCAGTGAGCTG	10043
rs752550816	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35324612	GGAGTGCAGTGGCAC[C/T]ATCTAGGCTCACTGC	10043
rs752615990	snp	C/T	1.64944e-05	0.00287175	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334335	CCCTGCAGACCTGGG[C/T]TCCAGCAGTGTGAGA	10043
rs752628698	snp	A/G	1.74977e-05	0.00295779	intron-variant	TOM1	GRCh38.p7	22:35333538	CTGAGGGTACATTAT[A/G]GTACTGTGGGCACCC	10043
rs752708440	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35325831	TCGAGAGTCCCCTTT[C/T]GTCTCTTGGGACATG	10043
rs752709823	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35313675	TCCATGAGGGGCAGG[C/T]GGGTCTTGCCATCAT	10043
rs752739099	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35314421	AGCTTGCCTGCACTG[C/T]TTGGGTCACATCAGA	10043
rs752766189	snp	C/G	1.6974e-05	0.0029132	intron-variant	TOM1	GRCh38.p7	22:35330486	GCCATGAACGGTAGC[C/G]CCAGCACCTCCCCTG	10043
rs752828989	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35306117	TCACGTAATTTTCAC[A/G]TATCATGAAATATTA	10043
rs752895917	snp	A/G	4.3536e-05	0.00466542	intron-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35321822	GATTCTGATGTGATC[A/G]GAACCTGGCTGGATA	10043
rs752899583	snp	A/G	1.76649e-05	0.00297189	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35323894	TCCGGTGACACGCCC[A/G]TAGCACCAACCCCGG	10043
rs752962669	snp	C/T	1.64923e-05	0.00287156	intron-variant	TOM1	GRCh38.p7	22:35345805	TTGGGGCCCACTCCT[C/T]ACCCACACAGCAGGA	10043
rs752974181	snp	C/T			intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35335418	TGTTAGCTGTATCTT[C/T]CTTTAGTCTGGGCAG	10043
rs752986404	snp	G/T			intron-variant	TOM1	GRCh38.p7	22:35307178	CTCCAAACTTCTGTC[G/T]TTCATGTAGCTCATT	10043
rs752987703	snp	C/T	1.64751e-05	0.00287007	missense, nc-transcript-variant, intron-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35321961	TTGTCCTCCTTAGTC[C/T]CAAAGATGCCCTCCG	10043
rs752997428	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35311170	GCCAGGTCTCAGTGC[C/T]GGCTCCCGAGGGCTT	10043
rs753011753	in-del	-/TTT			intron-variant	TOM1	GRCh38.p7	22:35302331	TTCTTTTTCTTTTTC[-/TTT]TTTTTTTTTTTTTTT	10043
rs753031196	in-del	-/TGT			upstream-variant-2KB	TOM1	GRCh38.p7	22:35298698	CTCAGCCTCCCAAAA[-/TGT]TGGGATTACAGGCGT	10043
rs753067853	snp	C/G	1.64846e-05	0.0028709	intron-variant	TOM1	GRCh38.p7	22:35317865	ACTTTATGACTCCTG[C/G]TTTCTTCTCAGAGAA	10043
rs753210443	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35341582	GGCCACCTGGCCTCT[C/T]GTGGTCAGAGGTTGA	10043
rs753240085	snp	A/G			upstream-variant-2KB	TOM1	GRCh38.p7	22:35298935	TGTAGGTGTCAGCAG[A/G]CACACCACACACAGC	10043
rs753257434	snp	G/T			intron-variant	TOM1	GRCh38.p7	22:35328658	ACAGGATGTTGAAAG[G/T]CACCCGCCCTGTCCC	10043
rs753274783	snp	C/T	1.65707e-05	0.00287838	intron-variant	TOM1	GRCh38.p7	22:35323481	TACCGGCTGTGTCCC[C/T]TTGTCCCCTCTCAGT	10043
rs753331109	snp	C/T	1.66413e-05	0.0028845	intron-variant	TOM1	GRCh38.p7	22:35322082	AGGACTACGGTCCAC[C/T]GAAAGTCACCTCCCC	10043
rs753371159	snp	A/G	1.68695e-05	0.00290422	synonymous-codon, nc-transcript-variant	TOM1	GRCh38.p7	22:35327375	CGAGCCCGCAGACCT[A/G]GAGCTGCTGCAGGTG	10043
rs753378696	snp	G/T	0.00226289	0.0335608	intron-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35338696	AGCATCCAATGGCTT[G/T]GTGGTCTCTCTTTCA	10043
rs753458638	snp	G/T			intron-variant	TOM1	GRCh38.p7	22:35333125	GTGCTGTCTTATCCA[G/T]GCCCATAGAGAAATC	10043
rs753470504	snp	A/G	3.29495e-05	0.00405877	synonymous-codon, nc-transcript-variant	TOM1	GRCh38.p7	22:35327291	GAAGCTGCGCAGTGA[A/G]CTGGAGATGGTGAGT	10043
rs753518638	in-del	-/C	1.67304e-05	0.00289222	intron-variant	TOM1	GRCh38.p7	22:35333391	ATGATCAGGGCATCT[-/C]CCTTCCCACCAGGCC	10043
rs753565943	snp	C/G	1.65337e-05	0.00287517	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35338767	TGGAGCCCTGGACGC[C/G]CGGCAGCAGAGCACT	10043
rs753632416	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35325915	CCCATCTGATTTGGA[C/T]ACATGGGGTTTGTGA	10043
rs753678934	snp	C/T	8.55147e-05	0.00653835	intron-variant	TOM1	GRCh38.p7	22:35333520	TGGTTTGGAGGGCTC[C/T]AGCTGAGGGTACATT	10043
rs753686652	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35314618	ATGAGAGGTGCCCAT[C/T]GTTTTCAGGGGGTAC	10043
rs753773374	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35311282	CTCACTCCTTAAAGA[A/G]GAATATTAATCACGA	10043
rs753799675	snp	C/G			intron-variant	TOM1	GRCh38.p7	22:35307278	CTGTTAAAATTTGAC[C/G]TCATCCTATATAATT	10043
rs753829882	snp	A/C			intron-variant	TOM1	GRCh38.p7	22:35345905	AGAGCAGAGGGGCAC[A/C]CTTAAAGTCCCCATC	10043
rs753834065	snp	A/C			intron-variant	TOM1	GRCh38.p7	22:35315528	AAAGAAGCCACACTC[A/C]GTAAACCTTCACAGG	10043
rs753840370	snp	A/G	1.66302e-05	0.00288355	intron-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35321806	AGCAATGGGCTAGGA[A/G]GATTCTGATGTGATC	10043
rs753856651	snp	A/T			intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35335516	GAGGCTACCCTGCAA[A/T]GGCAAGCTAATGAGT	10043
rs753861150	snp	C/T	6.59337e-05	0.0057413	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35345735	TCCAGATCCCAGTCA[C/T]CCAGGCCTGCCTCAT	10043
rs753861824	in-del	-/G			intron-variant	TOM1	GRCh38.p7	22:35308167	TTTTCAACTTGCTAA[-/G]CCTTCACACCTGCAT	10043
rs753869647	snp	C/G	1.67209e-05	0.00289139	intron-variant	TOM1	GRCh38.p7	22:35333392	TGATCAGGGCATCTC[C/G]CTTCCCACCAGGCCC	10043
rs754031352	snp	A/G	1.64885e-05	0.00287123	intron-variant	TOM1	GRCh38.p7	22:35323651	AGAACTGCCGTACCG[A/G]GAACCAAGGGAAGGG	10043
rs754065345	snp	C/T			intron-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35337520	CAGCTAGTGGTCACA[C/T]TCCACCAGCAAACTC	10043
rs754120930	snp	A/G	1.65056e-05	0.00287272	intron-variant	TOM1	GRCh38.p7	22:35317994	AGAGGTTGGGGGCAG[A/G]GACGGCCATCCCACC	10043
rs754140635	snp	C/T	1.68508e-05	0.0029026	stop-gained, nc-transcript-variant	TOM1	GRCh38.p7	22:35323798	GAGACACAATCAGGA[C/T]AGGATTCTGTGGGCA	10043
rs754296213	snp	A/G			missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35347093	CGGGCCAAAGCCGCG[A/G]ACCGATTGCCCAACC	10043
rs754298197	snp	G/T			intron-variant	TOM1	GRCh38.p7	22:35317722	ATGTGTATAGAGCAG[G/T]CTCACACAGGGCCAG	10043
rs754318553	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35328725	CCTTGGAGGGGGCAG[A/G]GGACAGGGTCCACAT	10043
rs754322284	snp	A/G	1.67122e-05	0.00289064	intron-variant, utr-variant-5-prime, nc-transcript-variant	TOM1	GRCh38.p7	22:35299907	CTGATTCCCGGGGTT[A/G]GTGGCAGCGGCGGTA	10043
rs754426884	snp	C/G			intron-variant	TOM1	GRCh38.p7	22:35317721	AATGTGTATAGAGCA[C/G]TCTCACACAGGGCCA	10043
rs754435263	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35342190	CGCAGCCCAGGTTTG[C/T]GCCCTGGGATTCAGA	10043
rs754495829	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35300576	CAAATGGACCCGCAC[A/G]GACTCTCAGAACCTG	10043
rs754513314	in-del	-/CA			intron-variant	TOM1	GRCh38.p7	22:35318993	TGTGGGCATCTGAGT[-/CA]CACAGTCAAGGCCCA	10043
rs754571706	in-del	-/A	1.66693e-05	0.00288693	intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334284	CAGCAGCTCACACAC[-/A]AGCTTGTGGATGGGT	10043
rs754587941	snp	C/G			intron-variant	TOM1	GRCh38.p7	22:35313640	AGGTCAGGCCAGACT[C/G]GTCCCACTCCACCCT	10043
rs754633511	snp	C/T	1.64746e-05	0.00287002	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35327299	GCAGTGAGCTGGAGA[C/T]GGTGAGTGGGAACGT	10043
rs754651567	snp	A/T			intron-variant	TOM1	GRCh38.p7	22:35326469	TGGAACCCTTTGACC[A/T]TTGAAAACCTGCCCA	10043
rs754667806	in-del	-/AAAT			upstream-variant-2KB	TOM1	GRCh38.p7	22:35297384	TCTGTCTTTAAAAAT[-/AAAT]AAATAAATAAATCCA	10043
rs754719274	snp	A/C			intron-variant	TOM1	GRCh38.p7	22:35330264	TCCAGCCTGGGCGAC[A/C]GAGCTCCGTCTCACA	10043
rs754751420	snp	C/G	1.71243e-05	0.00292607	intron-variant	TOM1	GRCh38.p7	22:35333522	GTTTGGAGGGCTCCA[C/G]CTGAGGGTACATTAT	10043
rs754830013	snp	C/T			intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35335349	GATAACCTCTCCACA[C/T]CCACAAATCCAGGTC	10043
rs754841460	snp	A/T	3.29728e-05	0.00406021	intron-variant	TOM1	GRCh38.p7	22:35323654	ACTGCCGTACCGGGA[A/T]CCAAGGGAAGGGAGG	10043
rs754853608	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35322167	AGGTCTGTAGGCAAC[A/G]CACTGTCCTGTCTAC	10043
rs754908920	snp	A/G	0.000269879	0.0116132	intron-variant	TOM1	GRCh38.p7	22:35322959	CACAGGAGGAGCCAC[A/G]AGGGTGGGGGTTCTG	10043
rs754926696	snp	C/T	1.66286e-05	0.0028834	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35347102	GCCGCGGACCGATTG[C/T]CCAACCTCTCCAGCC	10043
rs754946902	snp	A/G	1.66214e-05	0.00288278	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35333420	CCCCAAGTGAGGCCG[A/G]GCCGGCAGCTGACCT	10043
rs754988570	snp	C/G	1.64827e-05	0.00287073	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35345737	CAGATCCCAGTCACC[C/G]AGGCCTGCCTCATGG	10043
rs755034808	snp	C/T	4.94344e-05	0.00497139	missense, intron-variant, nc-transcript-variant	TOM1	GRCh38.p7	22:35323596	TCCCCATGACTGACC[C/T]GGACATGCTGTCACC	10043
rs755154240	snp	A/C			intron-variant	TOM1	GRCh38.p7	22:35332481	CACGACTTGAACAGA[A/C]CCCACACTAAAGTCT	10043
rs755182744	snp	C/G	1.65089e-05	0.00287301	intron-variant	TOM1	GRCh38.p7	22:35345684	CACGTCTTCCACCTT[C/G]TCACCTAGGGCACTG	10043
rs755260120	in-del	-/GT			intron-variant, downstream-variant-500B	TOM1, MIR6069	GRCh38.p7	22:35336678	GGAGCACTTAGACAA[-/GT]GTCACCCCAGTGGCC	10043
rs755284759	snp	G/T	0.000127445	0.00798163	intron-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35321807	GCAATGGGCTAGGAA[G/T]ATTCTGATGTGATCA	10043
rs755344935	snp	A/T			intron-variant	TOM1	GRCh38.p7	22:35310301	GGCTCACGCCTGTAA[A/T]CCCAGCACTTTGGGA	10043
rs755368477	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35308843	TAACATTGTGGGTTG[C/T]GGAAGCAATACCCTC	10043
rs755396669	snp	A/G			intron-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35337929	GGGCACCCCCACTGC[A/G]GCAGCTGGGAAAGAC	10043
rs755397578	in-del	-/ACACCTACACACACACCACATGCATCT			intron-variant	TOM1	GRCh38.p7	22:35343736	ACATCTACACCCACC[-/ACACCTACACACACACCACATGCATCT]ACACCTACACACACA	10043
rs755406722	snp	G/T	0.000195561	0.00988646	intron-variant, utr-variant-5-prime, nc-transcript-variant	TOM1	GRCh38.p7	22:35299908	TGATTCCCGGGGTTG[G/T]TGGCAGCGGCGGTAG	10043
rs755480828	snp	A/T	1.65578e-05	0.00287726	missense, nc-transcript-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35323100	CAGGACTTCGTGGAG[A/T]GTGTGCTGGTGAGGA	10043
rs755494045	snp	C/T	3.54459e-05	0.00420971	utr-variant-3-prime, nc-transcript-variant	TOM1	GRCh38.p7	22:35347242	CTGCAGCCCAGGTCC[C/T]CACTGCTCTCACACC	10043
rs755501340	snp	C/G	1.67868e-05	0.00289709	intron-variant	TOM1	GRCh38.p7	22:35323198	TGCCAGGACAGGGCA[C/G]GGCACGGCCAGGAAG	10043
rs755522669	snp	A/G			upstream-variant-2KB	TOM1	GRCh38.p7	22:35298824	ACAATAAGTACTTAA[A/G]CACCCACAGTAGCCA	10043
rs755594837	snp	C/T	3.29544e-05	0.00405908	synonymous-codon, nc-transcript-variant, intron-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35322010	CGTGGGGAATAAGAA[C/T]TTCCACGAGGTGATG	10043
rs755598296	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35340686	CAGGAGGTGGAGGTT[A/G]TGGTGAGCTGAGATT	10043
rs755636415	snp	C/T	1.64768e-05	0.00287021	intron-variant	TOM1	GRCh38.p7	22:35327261	CACCACGATCAACTG[C/T]GTGTTTCAGATTGGG	10043
rs755648617	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35331713	ACATGGTGAAACCCC[A/G]TCTCTACTAAAAAAT	10043
rs755663564	in-del	-/CAGGG	1.67461e-05	0.00289357	intron-variant	TOM1	GRCh38.p7	22:35323190	AGGTGAGTGCCAGGA[-/CAGGG]CAGGGCAGGGCACGG	10043
rs755670421	snp	G/T			intron-variant	TOM1	GRCh38.p7	22:35302951	AATTCTGTAAACCAG[G/T]CCCCTCCTTGCTGCA	10043
rs755709789	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35319213	AGCTGCAAGTCACTG[C/T]AGTATCCTTGGGGAC	10043
rs755709838	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35333106	TAGTAAACTGGACAG[A/G]GTGGTGCTGTCTTAT	10043
rs755744384	snp	C/T	6.61212e-05	0.00574945	intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334485	TGGTCCCCTGCAGTT[C/T]GGGTGGCTCTCGGGG	10043
rs755761907	snp	C/T			missense, nc-transcript-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334375	CAGTCTCTGGAGGCC[C/T]CTGGTCGACTGGAAG	10043
rs755834590	snp	A/G	1.81023e-05	0.00300846	intron-variant	TOM1	GRCh38.p7	22:35323923	GGAACAGGTAAACGA[A/G]CCTGGGGTCAGAACC	10043
rs755837687	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35323249	CCTGCCCAGTGGAGA[A/G]TCGAGGCCATCGTGT	10043
rs755911133	snp	C/T			intron-variant, downstream-variant-500B	TOM1, MIR6069	GRCh38.p7	22:35336573	ACAGCAGAGACGCCT[C/T]GGCTAGGCCTTCACA	10043
rs755922213	snp	G/T			utr-variant-3-prime, nc-transcript-variant	TOM1	GRCh38.p7	22:35347900	GGCACCACAGCACTG[G/T]GGCTCACCTCTTGGT	10043
rs755931626	in-del	-/AGTGCC	1.64727e-05	0.00286986	intron-variant	TOM1	GRCh38.p7	22:35333066	TTCATGGGAAGAAGG[-/AGTGCC]AGTGCCATTCTCACC	10043
rs756006812	snp	C/T	1.66103e-05	0.00288182	intron-variant	TOM1	GRCh38.p7	22:35322077	GTGGCAGGACTACGG[C/T]CCACTGAAAGTCACC	10043
rs756045190	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35313698	GCCATCATGCCAGGC[A/G]GATTATCTGGAGCCC	10043
rs756078210	in-del	-/C			intron-variant	TOM1	GRCh38.p7	22:35339903	AGCGAGACTCCGTCT[-/C]AAAAAAAAAAAAAAG	10043
rs756133636	snp	C/T			utr-variant-3-prime, nc-transcript-variant	TOM1	GRCh38.p7	22:35347867	TGCCCTCCATCCTTC[C/T]TCTGTTCCTTCTGGC	10043
rs756145508	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35305378	GAAAGAAACTGATGG[C/T]GGGCCAGGCACGGTG	10043
rs756190773	snp	A/G	3.2981e-05	0.00406071	intron-variant	TOM1	GRCh38.p7	22:35317976	GGTAAGGGCCCCCCA[A/G]GGAGAGGTTGGGGGC	10043
rs756194101	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35317591	CACACGGAGGCCCAC[C/T]TAGATTCCCCTCTGG	10043
rs756245541	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35307206	ATTTGTGATTTGTGT[C/T]TACCCCCATGCCACC	10043
rs756249063	snp	C/G	1.67284e-05	0.00289205	intron-variant	TOM1	GRCh38.p7	22:35338802	CGGTAAGCAGAGGGG[C/G]CATCCTGCCACCCTG	10043
rs756345269	snp	A/G			intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35335501	GTTAGGGGTGCTGCC[A/G]AGGCTACCCTGCAAA	10043
rs756364078	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35317207	TTGTTTGTTTGTTTG[C/T]TTTGGAGATGGAGTT	10043
rs756407724	in-del	-/GT			upstream-variant-2KB	TOM1	GRCh38.p7	22:35297841	gtttttttttgtttt[-/GT]ttttttttttttttt	10043
rs756421009	in-del	-/CTA			intron-variant	TOM1	GRCh38.p7	22:35343741	CTACACCCACCACAC[-/CTA]CACACACACCCCTAC	10043
rs756456409	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35311177	CTCAGTGCCGGCTCC[C/T]GAGGGCTTCAGTGGA	10043
rs756558197	snp	A/G	1.64841e-05	0.00287085	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35345731	TCCTTCCAGATCCCA[A/G]TCACCCAGGCCTGCC	10043
rs756573571	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35327971	AAAAAGCACCCTCCC[C/T]ATGGAGGCCAGTCAT	10043
rs756574663	snp	C/G	6.64319e-05	0.00576295	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35347145	GGCCCCCGGGTCCCC[C/G]ATCTGGCCCAGCGCC	10043
rs756617322	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35321414	GCTGGAGTACAGTGG[C/T]GCAATCTCGGCTCTC	10043
rs756628567	snp	A/C			intron-variant	TOM1	GRCh38.p7	22:35328711	TCCCGGAGGCCTGAC[A/C]TTGGAGGGGGCAGGG	10043
rs756667480	snp	A/C	1.72698e-05	0.00293847	intron-variant	TOM1	GRCh38.p7	22:35330301	AAAAGAGACGGCCTC[A/C]CTCTGAGTCATGTGA	10043
rs756689543	snp	C/T	4.94401e-05	0.00497168	stop-gained, nc-transcript-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334381	CTGGAGGCCTCTGGT[C/T]GACTGGAAGATGAGT	10043
rs756741564	snp	A/G	6.85883e-05	0.00585572	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35323864	GCTGCCCCTCTGCCC[A/G]CCCCGCCCATACTCT	10043
rs756753096	snp	C/T	3.32768e-05	0.00407888	stop-gained, nc-transcript-variant	TOM1	GRCh38.p7	22:35330365	CTCAACCGCACGTGC[C/T]GAGCCATGCAGCAGC	10043
rs756755433	snp	A/G	1.69458e-05	0.00291078	intron-variant, nc-transcript-variant	TOM1	GRCh38.p7	22:35323008	ACCAAGGTGCTCGAC[A/G]GCACCTCTCGGCCCT	10043
rs756778467	snp	A/G			utr-variant-3-prime, nc-transcript-variant	TOM1	GRCh38.p7	22:35347375	GGCTGGGGGTGTGGA[A/G]GCAGTGGGATGAACT	10043
rs756778964	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35320547	CCTCTGCACCCAAGA[C/T]CTTGGTCCAGGCTCT	10043
rs756784696	snp	C/G	1.65113e-05	0.00287322	intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334466	GAGTGGCCTGGCCCT[C/G]CCCTGGTCCCCTGCA	10043
rs756832022	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35310426	GGCATGGTGGCACAC[A/G]CCTGTAGTCCCAGCT	10043
rs756850796	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35318371	CAAAAACAGACTTCC[A/G]TTTCCTTAAGATTTG	10043
rs756865303	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35321654	TCCACCTGCCTCAGC[C/T]TCCCAAAGTCCTGGG	10043
rs756889006	snp	A/C	1.81233e-05	0.00301021	intron-variant	TOM1	GRCh38.p7	22:35333549	TTATGGTACTGTGGG[A/C]ACCCCTGCAGATTTT	10043
rs756911084	snp	C/T	0.000677094	0.0183872	intron-variant, utr-variant-5-prime, nc-transcript-variant	TOM1	GRCh38.p7	22:35299896	GTTGCTGTCAGCTGA[C/T]TCCCGGGGTTGGTGG	10043
rs756997167	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35313863	AGGATTGCAGGGCCC[A/G]GTTCTGTCAGGAGCT	10043
rs757033778	snp	A/C	3.33673e-05	0.00408442	intron-variant	TOM1	GRCh38.p7	22:35346921	CCTCCTTTCCTTCTA[A/C]CTTCCCAGGGTAATG	10043
rs757036160	in-del	-/ACACACACACAT			intron-variant	TOM1	GRCh38.p7	22:35332596	CACTAACACACACAC[-/ACACACACACAT]ACACACACACAAATA	10043
rs757104780	snp	G/T	1.75755e-05	0.00296436	intron-variant	TOM1	GRCh38.p7	22:35330532	CCCCAACCCTCTCCC[G/T]TCCCTTCCTCCCTGT	10043
rs757176222	snp	C/G			intron-variant	TOM1	GRCh38.p7	22:35303867	AGTGGTTGTGCATGT[C/G]TGTCTCCACAGCTAG	10043
rs757346371	snp	A/G	1.64789e-05	0.0028704	synonymous-codon, intron-variant, nc-transcript-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35323567	TGAGGACCTGCGGAG[A/G]AAAGGCCTGGAGTTC	10043
rs757400563	snp	C/T	4.94181e-05	0.00497057	intron-variant	TOM1	GRCh38.p7	22:35332974	TCGTGTCTTTTCTGT[C/T]TTGTAGGTTTGAACG	10043
rs757520181	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35340727	ACTCCAGCCTGGGCA[A/G]TGGAGTAAGACCCTG	10043
rs757531876	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35343904	ACACACCTGCACACA[C/T]ACCCCTACACACACC	10043
rs757584955	snp	C/G			intron-variant	TOM1	GRCh38.p7	22:35330076	TGAGGTCAGGAGATC[C/G]AGACCACCCTGGCTA	10043
rs757629430	snp	C/T	1.65938e-05	0.00288039	missense, nc-transcript-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35338787	AGCAGAGCACTGGCG[C/T]GGTAAGCAGAGGGGC	10043
rs757635404	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35304846	TGTCAGCTTACCCCT[A/G]AGCACTTGGAGTCCA	10043
rs757644333	in-del	-/CA			intron-variant	TOM1	GRCh38.p7	22:35339903	AGCGAGACTCCGTCT[-/CA]AAAAAAAAAAAAAGA	10043
rs757717708	snp	G/T			intron-variant	TOM1	GRCh38.p7	22:35316718	TATTCAGTATTACAG[G/T]TGTACCAAATGCCAC	10043
rs757725290	snp	C/T	6.58989e-05	0.00573978	utr-variant-5-prime, synonymous-codon, nc-transcript-variant	TOM1	GRCh38.p7	22:35317897	GCCACAGATGGCTCC[C/T]TGCAGAGCGAGGACT	10043
rs757770544	snp	A/T			intron-variant	TOM1	GRCh38.p7	22:35317783	CCTCCTCCCCATCTC[A/T]TCCGGCCCTGCACCC	10043
rs757823744	snp	C/T	0.000136808	0.00826955	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35338722	TTTCAGGGTAAAATA[C/T]GAAGCCCCCCAAGCA	10043
rs757860202	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35315611	TCCAGGCCTGATCTA[A/G]GGGTAAAGCAACCGC	10043
rs757871154	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35311242	ACCGCGGAGCAGTCC[C/T]GTGGGAAGGCCAGGG	10043
rs757877286	snp	C/T	0.000123525	0.00785795	intron-variant	TOM1	GRCh38.p7	22:35333542	GGGTACATTATGGTA[C/T]TGTGGGCACCCCTGC	10043
rs757949241	snp	C/G			intron-variant	TOM1	GRCh38.p7	22:35322762	CAGAGACAGCATTGG[C/G]ATTCTGCGTGCACTG	10043
rs757982649	snp	C/T			upstream-variant-2KB	TOM1	GRCh38.p7	22:35299188	GATCTAATTCCAGTA[C/T]CTAGAGAAAATGGGA	10043
rs758004483	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35311838	GCTGACACTTCTTCA[C/T]TGAATGATGGCTGTC	10043
rs758061997	snp	A/C	3.34778e-05	0.00409119	intron-variant	TOM1	GRCh38.p7	22:35347019	CCCCAGGGCTCTGGC[A/C]TCAGGGCCTACCCTC	10043
rs758126845	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35303942	CCTCAGCACCTAGCA[C/T]GGTGCCTGGCACATA	10043
rs758129430	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35341909	TGCCTGCTCCTGGGG[C/T]GCTGGAGTTTGGCTG	10043
rs758148626	in-del	-/T			intron-variant	TOM1	GRCh38.p7	22:35304431	AAGGATTTCAAACCC[-/T]TTCCAGATATTCTCT	10043
rs758149749	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35329246	TAGGCACGAGCCACC[A/G]GGTGTAGCCATTTTT	10043
rs758200021	in-del	-/CAC			intron-variant	TOM1	GRCh38.p7	22:35343638	ACCCACACCTACACA[-/CAC]CACACCTATACTCAT	10043
rs758225957	snp	A/C	1.64827e-05	0.00287073	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35345741	TCCCAGTCACCCAGG[A/C]CTGCCTCATGGAGGA	10043
rs758247047	snp	G/T			intron-variant	TOM1	GRCh38.p7	22:35346215	GGAAGCACCCAGGAG[G/T]AGGAGGGCGGGTGCC	10043
rs758279472	snp	A/G	4.24169e-05	0.00460507	intron-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35321823	ATTCTGATGTGATCA[A/G]AACCTGGCTGGATAC	10043
rs758300139	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35333532	CTCCAGCTGAGGGTA[C/T]ATTATGGTACTGTGG	10043
rs758301872	snp	C/T			utr-variant-3-prime, nc-transcript-variant	TOM1	GRCh38.p7	22:35347281	GGGACCTCCCTCCCT[C/T]CTCTGGTGTTAAGGC	10043
rs758302817	in-del	-/T			intron-variant	TOM1	GRCh38.p7	22:35330945	GAATCCAGAGAAAAG[-/T]GAAACTGATGTCTCC	10043
rs758331810	snp	A/G	1.64841e-05	0.00287085	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334350	CTCCAGCAGTGTGAG[A/G]GCTGGCCTGCAGTCT	10043
rs758402338	snp	C/T	0.000104417	0.00722478	intron-variant	TOM1	GRCh38.p7	22:35330518	CCTCTGGCCTACTGC[C/T]CCAACCCTCTCCCTT	10043
rs758476188	snp	C/G/T	5.05151e-05	0.00502548	missense, synonymous-codon, nc-transcript-variant	TOM1	GRCh38.p7	22:35323836	CAGCCAGCAAGAGGA[C/G/T]TCTGGCCAGCATGCT	10043
rs758526638	snp	A/C/G	0.000218721	0.0104556	intron-variant	TOM1	GRCh38.p7	22:35323204	GACAGGGCAGGGCAC[A/C/G]GCCAGGAAGAGCTGT	10043
rs758529972	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35309636	GCAACAGAGTGAGAC[C/T]CCATCTCAAAAAAAA	10043
rs758559691	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35327508	CCTTGGTCACAGTTG[A/G]GGACATGTTACCACC	10043
rs758591727	snp	A/G			upstream-variant-2KB	TOM1	GRCh38.p7	22:35297322	GGAGATCAGGGCTAC[A/G]GTGAGCTACAGTTGT	10043
rs758603572	snp	C/T	1.64942e-05	0.00287173	intron-variant	TOM1	GRCh38.p7	22:35345809	GGCCCACTCCTCACC[C/T]ACACAGCAGGAGGAC	10043
rs758658028	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35331570	CAGTTCCTCTAAAGA[A/G]TACTTAGGTGCTATT	10043
rs758713411	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35319091	CCAAGGACTCATGAG[A/G]GTGAGGGTGAGGGAA	10043
rs758717719	snp	A/G	3.64485e-05	0.00426883	intron-variant	TOM1	GRCh38.p7	22:35323939	CCTGGGGTCAGAACC[A/G]TCAGGTCCAGGCAGG	10043
rs758797122	snp	C/T	1.65644e-05	0.00287783	intron-variant	TOM1	GRCh38.p7	22:35323483	CCGGCTGTGTCCCCT[C/T]GTCCCCTCTCAGTCC	10043
rs758800192	snp	A/G			intron-variant, downstream-variant-500B	TOM1, MIR3909	GRCh38.p7	22:35335779	TGTGAAGGGCTAAGT[A/G]CTGTCCTGGAGGGGG	10043
rs758803688	snp	A/G			upstream-variant-2KB	TOM1	GRCh38.p7	22:35298850	AGCCAGACTACTAAG[A/G]CCATGGTTATTGTAT	10043
rs758819306	snp	G/T	1.67626e-05	0.002895	intron-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35338707	GCTTGGTGGTCTCTC[G/T]TTCAGGGTAAAATAC	10043
rs758847495	snp	A/G			intron-variant, downstream-variant-500B	TOM1, MIR3909	GRCh38.p7	22:35335823	GGACACAGAGGAGGG[A/G]GCATGCAACTCTGCG	10043
rs758885009	snp	C/G	3.5073e-05	0.00418751	intron-variant	TOM1	GRCh38.p7	22:35300004	CTGGAGCCCCCCACA[C/G]CTCCGCCCCGGTGCT	10043
rs758905614	snp	A/G	6.42901e-05	0.00566929	intron-variant, utr-variant-5-prime, nc-transcript-variant	TOM1	GRCh38.p7	22:35299916	GGGGTTGGTGGCAGC[A/G]GCGGTAGCAGCAATG	10043
rs758913159	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35308485	GGCAGAGTTTCACCA[C/T]GTTGGCCAGGCTGGT	10043
rs759064716	snp	C/G	1.64844e-05	0.00287087	intron-variant	TOM1	GRCh38.p7	22:35317966	ACGGAGGAAGGGTAA[C/G]GGCCCCCCAAGGAGA	10043
rs759085181	snp	A/G	0.000132594	0.00814121	missense, nc-transcript-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35338769	GAGCCCTGGACGCCC[A/G]GCAGCAGAGCACTGG	10043
rs759098704	snp	C/T	1.67209e-05	0.00289139	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35330356	TGGCAGGAGCTCAAC[C/T]GCACGTGCCGAGCCA	10043
rs759116251	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35324064	TCTTCCTGTTTGAGC[A/G]ATGAGACTCAGAGAG	10043
rs759174674	snp	C/T	1.79493e-05	0.00299572	intron-variant	TOM1	GRCh38.p7	22:35327400	CAGGTGAGCAGGTGG[C/T]ACCACCCCCTGGGGC	10043
rs759198959	in-del	-/CACC			intron-variant	TOM1	GRCh38.p7	22:35327584	ACTTTCTGGTTTGAA[-/CACC]CAAAGTAGCCCCCCT	10043
rs759234825	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35330759	CACAGCTGAGAGCAC[A/G]GCCCTGCAACCAGAC	10043
rs759272685	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35315392	GACATGACTAACCCC[C/T]GCCCCAAAACCCTCC	10043
rs759285690	snp	C/G			intron-variant	TOM1	GRCh38.p7	22:35318711	AGCAGAAAGGGGATG[C/G]GAGGGTCCCTGTCCT	10043
rs759297607	snp	C/T	1.64928e-05	0.00287161	intron-variant	TOM1	GRCh38.p7	22:35345709	GCACTGCCTTACCCT[C/T]TGCCCTTCCTTCCAG	10043
rs759330819	snp	G/T			intron-variant, downstream-variant-500B	TOM1, MIR3909	GRCh38.p7	22:35335990	CTTCACACAGGGAAG[G/T]GGGCAGGATGCTGAG	10043
rs759358878	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35317525	GGGAGAACATCTTAT[C/T]TACAGAAATGAAGCA	10043
rs759364170	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35307128	GTTTAACTCTTTACT[A/G]CCTTACTAAGGAGAT	10043
rs759423891	snp	A/G	1.6507e-05	0.00287284	splice-acceptor-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334327	CTTTCTGTCCCTGCA[A/G]ACCTGGGCTCCAGCA	10043
rs759425193	snp	C/T	3.31779e-05	0.00407282	missense, nc-transcript-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35323061	AAGAACTGCGGGCAC[C/T]GCTTCCACGTGCTGG	10043
rs759461558	snp	C/T	1.69861e-05	0.00291424	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35347198	GATGATGACATGCTG[C/T]TTGCCTTATGAGTGT	10043
rs759480857	snp	C/G			intron-variant	TOM1	GRCh38.p7	22:35342193	AGCCCAGGTTTGCGC[C/G]CTGGGATTCAGAGCA	10043
rs759517096	snp	C/T	1.65853e-05	0.00287964	missense, nc-transcript-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35323139	CCCAAGAACAACCCA[C/T]CCACCATCGTGCATG	10043
rs759540727	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35339643	GGCGCAGTGGCTCAC[A/G]CCTGTAATCCCAGCA	10043
rs759639799	snp	C/T	6.59652e-05	0.00574267	intron-variant	TOM1	GRCh38.p7	22:35345801	TATGTTGGGGCCCAC[C/T]CCTCACCCACACAGC	10043
rs759652887	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35341537	TCGGAACCAACACAC[C/T]GCGAGCCTGCTGTAG	10043
rs759674633	in-del	-/TT	0.0537957	0.154932	intron-variant	TOM1	GRCh38.p7	22:35331273	GCTAATTTTCTTTTC[-/TT]TTTTTTTTTTTCTTT	10043
rs759732497	snp	G/T			intron-variant	TOM1	GRCh38.p7	22:35329731	CCTTTGCAGACTCAG[G/T]TTTTTTTTGACTAAG	10043
rs759777404	snp	A/T			intron-variant	TOM1	GRCh38.p7	22:35301271	ACGCACACATATATA[A/T]AAAAATATACACATA	10043
rs759785188	in-del	-/A			intron-variant	TOM1	GRCh38.p7	22:35325011	TTGTGGAGTGCCATG[-/A]GCTGCTGTATCTGCT	10043
rs759796857	snp	A/G	1.68388e-05	0.00290158	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35323799	AGACACAATCAGGAC[A/G]GGATTCTGTGGGCAC	10043
rs759836435	snp	A/G			upstream-variant-2KB	TOM1	GRCh38.p7	22:35298276	AGTAGCCCAGCCCCC[A/G]GGGACATCCAGACTC	10043
rs759894563	snp	A/G/T	0.000105697	0.00726893	synonymous-codon, nc-transcript-variant	TOM1	GRCh38.p7	22:35323890	ACTCTCCGGTGACAC[A/G/T]CCCATAGCACCAACC	10043
rs759938389	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35321555	AGGGTCATACCACCA[C/T]GCCCGGCAAATTTTT	10043
rs759993369	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35322477	GCCCAGATCTCAGGG[C/T]GGCCAGACACACGTG	10043
rs760037000	snp	A/C/G	3.30192e-05	0.00406309	intron-variant	TOM1	GRCh38.p7	22:35322049	CACAGTGAGTGCCCC[A/C/G]TCTGTCTGTCCTGTG	10043
rs760045148	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35311132	CAGCTGAGCTGGTGA[A/G]TGGGAGTGGGAGGAA	10043
rs760153398	snp	A/G	1.64735e-05	0.00286993	intron-variant	TOM1	GRCh38.p7	22:35332944	TGGGGGCCTGTCTCA[A/G]TCTGTCTCCATAACT	10043
rs760191015	snp	G/T			intron-variant	TOM1	GRCh38.p7	22:35346987	AGTAGTCCCCGCCCC[G/T]GCCCGCCCTCTCCTT	10043
rs760254304	snp	G/T	1.64811e-05	0.00287059	stop-gained, nc-transcript-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35317957	ATCAACGAGACGGAG[G/T]AAGGGTAAGGGCCCC	10043
rs760301150	snp	G/T			intron-variant	TOM1	GRCh38.p7	22:35315468	GCTCTGTTCTTCCCA[G/T]GTGGCTCTATAAGTG	10043
rs760400373	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35310860	CAAAGAGATCGCCCA[A/G]CAGAGTTATTTTAAT	10043
rs760452243	snp	C/T	3.2987e-05	0.00406108	intron-variant	TOM1	GRCh38.p7	22:35317859	CTCATGACTTTATGA[C/T]TCCTGGTTTCTTCTC	10043
rs760572052	snp	C/T	0.000116806	0.00764129	synonymous-codon, nc-transcript-variant	TOM1	GRCh38.p7	22:35327366	CACCCAGGCCGAGCC[C/T]GCAGACCTGGAGCTG	10043
rs760572851	snp	A/C/T	4.99225e-05	0.00499591	synonymous-codon, stop-gained, nc-transcript-variant	TOM1	GRCh38.p7	22:35347096	GCCAAAGCCGCGGAC[A/C/T]GATTGCCCAACCTCT	10043
rs760595118	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35339615	AGAGGAATAAAAGAG[C/T]GGACCCTGGCCAGGC	10043
rs760659874	snp	C/T	1.7112e-05	0.00292501	intron-variant	TOM1	GRCh38.p7	22:35330326	ATGTGACTGTGGTTG[C/T]CTCACTTCCTTTCCT	10043
rs760661472	in-del	-/AG			upstream-variant-2KB	TOM1	GRCh38.p7	22:35297363	GCCAGCCTGGGTGAC[-/AG]AGACTCTGTCTTTAA	10043
rs760661822	snp	A/C	1.79383e-05	0.0029948	intron-variant	TOM1	GRCh38.p7	22:35322985	TTCTGAGCACCTCCT[A/C]TCCTCTGACCAAGGT	10043
rs760667426	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35344323	CCTGCCAGGCATGGG[C/T]GTGGGGCACCGTGCT	10043
rs760830531	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35329867	CTAACACTTGGAAGT[A/G]AAGTTCAAGTTCATG	10043
rs760885543	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35330838	TTAGACAAGTGACTT[C/T]ACTGCTGCAAGCTAC	10043
rs760961756	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35308073	AACAAGAGGGAACTT[A/G]GCCAGCAGGCTCCCC	10043
rs760967997	in-del	-/T	1.71749e-05	0.00293038	intron-variant	TOM1	GRCh38.p7	22:35330500	CCCCAGCACCTCCCC[-/T]GGCCTCTGGCCTACT	10043
rs760970255	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35319561	GAGAAGGCGTCCAAC[A/G]AGGACGCTGTCCCTG	10043
rs760987789	in-del	-/C			intron-variant	TOM1	GRCh38.p7	22:35327772	GAGATTTACACCATT[-/C]AGAATCCGAGACTCA	10043
rs761045294	snp	C/T	1.6713e-05	0.00289072	intron-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35321800	CTGCTAAGCAATGGG[C/T]TAGGAAGATTCTGAT	10043
rs761119697	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35300214	AGTAGGTAAGGAGAG[A/G]GGGTGGGTCCGGATG	10043
rs761139519	snp	G/T	1.67598e-05	0.00289476	synonymous-codon, nc-transcript-variant	TOM1	GRCh38.p7	22:35330469	CAACAATGTGTTCCT[G/T]CGCCATGAACGGTAG	10043
rs761281135	in-del	-/TGGCACACCA			intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334522	AACCCGGTTTTATGG[-/TGGCACACCA]TGAGGAAGGGCACAC	10043
rs761314467	snp	C/T	3.30136e-05	0.00406273	intron-variant	TOM1	GRCh38.p7	22:35345790	CACTGACGTGGTATG[C/T]TGGGGCCCACTCCTC	10043
rs761410442	snp	A/C			intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334226	CACCCACACGTGCCA[A/C]TTCCCCAGCACCAAG	10043
rs761517973	snp	A/G	4.99729e-05	0.0049984	missense, nc-transcript-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35323167	ATGACAAAGTGCTCA[A/G]CCTCATCCAGGTGAG	10043
rs761519247	snp	C/T	1.65485e-05	0.00287645	intron-variant	TOM1	GRCh38.p7	22:35322063	CATCTGTCTGTCCTG[C/T]GGCAGGACTACGGTC	10043
rs761582915	snp	C/G			upstream-variant-2KB	TOM1	GRCh38.p7	22:35298482	CTGTCACCCAGGCTG[C/G]AGTGCAGTGGCACGA	10043
rs761645107	snp	A/G	0.000197964	0.00994701	synonymous-codon, nc-transcript-variant	TOM1	GRCh38.p7	22:35327339	GTCGGAGATGCTGAC[A/G]GAGCTGGTGCCCACC	10043
rs761653052	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35332978	GTCTTTTCTGTCTTG[C/T]AGGTTTGAACGGTTC	10043
rs761700288	in-del	-/AA	4.94173e-05	0.00497053	intron-variant	TOM1	GRCh38.p7	22:35333017	CCAGACCACCAAGGT[-/AA]AAGTCTTCTTTTCTG	10043
rs761710485	snp	A/G	5.51212e-05	0.00524953	intron-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35338672	CTTGCATCAGCCATC[A/G]GTAAGGGCAGCATCC	10043
rs761717841	snp	A/C	1.64814e-05	0.00287061	intron-variant	TOM1	GRCh38.p7	22:35327246	AACCCTGGCTTCTCT[A/C]ACCACGATCAACTGT	10043
rs761791915	snp	C/T	1.65266e-05	0.00287455	intron-variant	TOM1	GRCh38.p7	22:35317841	TTACCCATTCAGGAC[C/T]CCCTCATGACTTTAT	10043
rs761800192	snp	A/G	0.000134382	0.00819589	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35338749	AGCAACAGACGGCCT[A/G]GCTGGAGCCCTGGAC	10043
rs761864828	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35346349	GTCTCTGGGCACCAA[A/G]GCCCACATGGGCACT	10043
rs762046267	snp	C/T	1.84653e-05	0.00303848	intron-variant	TOM1	GRCh38.p7	22:35322977	GGTGGGGGTTCTGAG[C/T]ACCTCCTCTCCTCTG	10043
rs762068881	in-del	-/G			intron-variant	TOM1	GRCh38.p7	22:35344289	GCCACCCGGAAAGCT[-/G]GGGGGTGCTCGCAGG	10043
rs762071134	snp	A/C			intron-variant	TOM1	GRCh38.p7	22:35313438	TGGTGACTACTCATT[A/C]TTTCTCTTGGCCCAA	10043
rs762136881	in-del	-/CAGT			upstream-variant-2KB	TOM1	GRCh38.p7	22:35298766	CATCCAAAATTTGTG[-/CAGT]CAATTTACTAGCCTT	10043
rs762162733	snp	A/G	0.000972815	0.0220332	intron-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35321767	GCTGGAGGTCCAGGG[A/G]CCACAGGTTGTGAGT	10043
rs762268413	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35344431	GGCTCAGGCTGTTTC[C/T]GGGTTGGCCCGGCCA	10043
rs762272840	snp	C/T	3.29761e-05	0.00406041	intron-variant	TOM1	GRCh38.p7	22:35323644	GGGTGAGAGAACTGC[C/T]GTACCGGGAACCAAG	10043
rs762290638	snp	A/G	9.89038e-05	0.00703151	splice-acceptor-variant	TOM1	GRCh38.p7	22:35345724	CTGCCCTTCCTTCCA[A/G]ATCCCAGTCACCCAG	10043
rs762323548	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35330987	GAAAGATGGATCCCA[A/G]GGCAGCTCAGATGTC	10043
rs762359033	snp	C/G	1.64885e-05	0.00287123	intron-variant	TOM1	GRCh38.p7	22:35317972	GAAGGGTAAGGGCCC[C/G]CCAAGGAGAGGTTGG	10043
rs762360815	snp	A/T	1.70119e-05	0.00291644	intron-variant	TOM1	GRCh38.p7	22:35323763	TCCTGTTTTCCTCCC[A/T]CTAGACCGTGTTCAA	10043
rs762401511	snp	C/G			intron-variant	TOM1	GRCh38.p7	22:35301468	ACCCAAACAGCCACA[C/G]TTCTCCGGAGGATGG	10043
rs762519557	snp	A/C			intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35335225	CCAGGATTCTTATAG[A/C]TAAGGAAAGTTCTAG	10043
rs762563338	snp	A/G	1.73993e-05	0.00294947	utr-variant-3-prime, nc-transcript-variant	TOM1	GRCh38.p7	22:35347222	TGAGTGTGGGGTCTG[A/G]CACCCTGCAGCCCAG	10043
rs762573871	snp	A/G			intron-variant, downstream-variant-500B	TOM1, MIR3909	GRCh38.p7	22:35335906	CACTAGGAACAGCAT[A/G]TGCAAAGTCTCAGAG	10043
rs762708424	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35329481	AAGGGGAAGCCAGGG[C/T]CAAGGGTATATGGGA	10043
rs762734069	snp	G/T			intron-variant	TOM1	GRCh38.p7	22:35328415	TATATGTGGACACTT[G/T]GTTCACATCGCTCAC	10043
rs762755248	snp	C/T	1.66051e-05	0.00288137	intron-variant	TOM1	GRCh38.p7	22:35323460	GGCTCACAGGTGAGC[C/T]GTGGTTACCGGCTGT	10043
rs762759612	snp	A/T			intron-variant	TOM1	GRCh38.p7	22:35305804	TTGCAAAGATGGAAC[A/T]GGCTGCCTTGTTCAG	10043
rs762789134	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35316324	ATGTGTGTAATGGAA[C/T]GTTACCTGCAAGAAA	10043
rs762839850	snp	C/T	1.67027e-05	0.00288982	intron-variant, missense, nc-transcript-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35299966	CGTTCAGCTCTCCAG[C/T]GGGACAGCGCATCGG	10043
rs762864428	snp	A/G	1.64996e-05	0.0028722	missense, nc-transcript-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334442	CACTGGCTGACCAAC[A/G]GAAAGAGTGAGTGGC	10043
rs762891976	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35306861	CACTGGCTGGGTGGC[C/T]ACCACATTCACAGAC	10043
rs762951289	snp	A/G	8.40824e-05	0.00648337	intron-variant	TOM1	GRCh38.p7	22:35346894	CCGTACTGGGGGCCC[A/G]GCTAACCTCTGCCTC	10043
rs762964236	snp	A/C/T	3.34109e-05	0.00408712	intron-variant	TOM1	GRCh38.p7	22:35346979	GCGAAGGTAGTAGTC[A/C/T]CCGCCCCTGCCCGCC	10043
rs762972935	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35340344	ACCAGAGGACCTCAG[C/T]GCGGCTAGGAGCGCT	10043
rs762985586	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35311001	GAGACCTGACCTTTG[A/G]TCTGGGCTTAGGAGC	10043
rs763005369	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35316178	ATGAGTACTTTGCAT[A/G]TGACACTTGCAGGGG	10043
rs763072163	snp	G/T			intron-variant	TOM1	GRCh38.p7	22:35329780	CTTTATTCTGGAATC[G/T]GCACGAAGCCAAGTT	10043
rs763176053	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35341314	TACGCTTCGCAGTAC[C/T]GCCATGTCCTCATCC	10043
rs763195415	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35340230	GGGTGGTGGACCTGG[A/G]GCCGAGGAGGCTAGA	10043
rs763196398	snp	A/G	1.64822e-05	0.00287068	intron-variant	TOM1	GRCh38.p7	22:35327230	GTAACATGGGCCCCA[A/G]AACCCTGGCTTCTCT	10043
rs763219136	snp	C/G			upstream-variant-2KB	TOM1	GRCh38.p7	22:35298683	AGGTGATCCACCTGC[C/G]TCAGCCTCCCAAAAT	10043
rs763244921	snp	G/T			intron-variant	TOM1	GRCh38.p7	22:35300639	AGCCCATCTCGGTGC[G/T]CCGTAGGTGGGGCAG	10043
rs763269373	snp	C/G/T	6.59776e-05	0.00574326	intron-variant	TOM1	GRCh38.p7	22:35345813	CACTCCTCACCCACA[C/G/T]AGCAGGAGGACCCGT	10043
rs763314023	snp	A/G	3.29625e-05	0.00405958	missense, intron-variant, nc-transcript-variant	TOM1	GRCh38.p7	22:35323626	CCATCCACACACCCC[A/G]GAGGGTGAGAGAACT	10043
rs763328082	snp	C/G			intron-variant	TOM1	GRCh38.p7	22:35332854	CAGGGCACACCAGAC[C/G]TGTCATCACCCTGAT	10043
rs763328166	snp	A/G	4.98649e-05	0.00499299	synonymous-codon, nc-transcript-variant	TOM1	GRCh38.p7	22:35346941	CCAGGGTAATGATGC[A/G]GAAGAGCCTAAGGGG	10043
rs763378506	in-del	-/A			intron-variant	TOM1	GRCh38.p7	22:35326322	TTCCCAGGCATTCCC[-/A]GTGTGCATGAGGGCA	10043
rs763381223	snp	C/T			intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334078	CCCCAGCAGAATCAA[C/T]GGATAGCGTTTTGAC	10043
rs763417558	snp	A/C	1.64727e-05	0.00286986	intron-variant	TOM1	GRCh38.p7	22:35333047	TGTGACTAGATCAGG[A/C]CCTGTTCATGGGAAG	10043
rs763449681	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35345893	TATAGCACCCTGAGA[A/G]CAGAGGGGCACACTT	10043
rs763490527	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35315489	TCTATAAGTGTGGAA[C/T]CCCCAAGGGCAGGGG	10043
rs763511484	snp	C/T	1.65957e-05	0.00288055	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35333455	GACATGGGCCCTGAC[C/T]CAGCAGCCACCGGCA	10043
rs763539486	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35323260	GAGAGTCGAGGCCAT[C/T]GTGTTTGTCCCAGGC	10043
rs763570062	snp	C/T	6.59163e-05	0.00574054	missense, intron-variant, nc-transcript-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35323562	ATCTATGAGGACCTG[C/T]GGAGGAAAGGCCTGG	10043
rs763644908	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35333108	GTAAACTGGACAGGG[C/T]GGTGCTGTCTTATCC	10043
rs763768588	snp	A/C	8.72821e-05	0.00660556	utr-variant-3-prime, nc-transcript-variant	TOM1	GRCh38.p7	22:35347225	GTGTGGGGTCTGGCA[A/C]CCTGCAGCCCAGGTC	10043
rs763798783	snp	C/G			intron-variant	TOM1	GRCh38.p7	22:35306198	CTGTAGCTCGAGTAC[C/G]ATACAAAACAGACTG	10043
rs763835229	snp	C/G	1.65778e-05	0.002879	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35330446	CTGCTCATCGTCAAT[C/G]ACAATCTCAACAATG	10043
rs763835880	snp	A/G	1.64825e-05	0.00287071	intron-variant	TOM1	GRCh38.p7	22:35327231	TAACATGGGCCCCAG[A/G]ACCCTGGCTTCTCTC	10043
rs763840152	snp	A/G			intron-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35337452	CAGCAGGGCCCTGCC[A/G]TAGTCACTGGCCCAC	10043
rs763902208	snp	C/T	1.78385e-05	0.00298646	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35323904	CGCCCATAGCACCAA[C/T]CCCGGAACAGGTAAA	10043
rs763961240	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35325864	AAGACATCAGGTGTG[C/T]AGTGATGTTACTCCC	10043
rs764071952	snp	C/G	6.65535e-05	0.00576822	intron-variant, missense, nc-transcript-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35299971	AGCTCTCCAGTGGGA[C/G]AGCGCATCGGTGAGT	10043
rs764118788	snp	C/T	0.000115305	0.00759205	intron-variant	TOM1	GRCh38.p7	22:35332962	TGTCTCCATAACTCG[C/T]GTCTTTTCTGTCTTG	10043
rs764206650	snp	A/G	1.69358e-05	0.00290992	intron-variant	TOM1	GRCh38.p7	22:35333357	GGGGCAGAAAGGAAC[A/G]AAGCTGCAGACAGCG	10043
rs764219591	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35330850	CTTCACTGCTGCAAG[C/T]TACACAAAACATTTC	10043
rs764219658	snp	A/C			intron-variant	TOM1	GRCh38.p7	22:35317667	AAGAGCAGAGGTACT[A/C]CGGCCTCAGTGGCTA	10043
rs764234669	snp	A/C	1.64735e-05	0.00286993	intron-variant	TOM1	GRCh38.p7	22:35346907	CCGGCTAACCTCTGC[A/C]TCCTTTCCTTCTACC	10043
rs764272494	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35318873	ATCCAGCTCTCCCGC[A/G]GCCAGTGCAGGGTTC	10043
rs764304250	snp	C/T	1.64757e-05	0.00287012	utr-variant-5-prime, synonymous-codon, nc-transcript-variant	TOM1	GRCh38.p7	22:35317884	CTTCTCAGAGAAAGC[C/T]ACAGATGGCTCCCTG	10043
rs764386798	snp	A/G	1.6483e-05	0.00287076	synonymous-codon, intron-variant, nc-transcript-variant	TOM1	GRCh38.p7	22:35323630	CCACACACCCCAGAG[A/G]GTGAGAGAACTGCCG	10043
rs764403238	snp	C/G	1.65395e-05	0.00287567	intron-variant	TOM1	GRCh38.p7	22:35322059	GCCCCATCTGTCTGT[C/G]CTGTGGCAGGACTAC	10043
rs764419024	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35311751	ACAAACCTCTGCACA[C/T]TGGCTGCCCCCACGA	10043
rs764470458	snp	G/T			intron-variant	TOM1	GRCh38.p7	22:35300219	GTAAGGAGAGAGGGT[G/T]GGTCCGGATGCCCAC	10043
rs764555099	snp	A/C/T	4.9464e-05	0.00497292	intron-variant	TOM1	GRCh38.p7	22:35317971	GGAAGGGTAAGGGCC[A/C/T]CCCAAGGAGAGGTTG	10043
rs764578585	snp	A/G	0.000131828	0.00811768	missense, intron-variant, nc-transcript-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35323563	TCTATGAGGACCTGC[A/G]GAGGAAAGGCCTGGA	10043
rs764602499	snp	A/G	1.67058e-05	0.00289009	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35330357	GGCAGGAGCTCAACC[A/G]CACGTGCCGAGCCAT	10043
rs764609922	snp	A/G	9.53698e-05	0.00690477	missense, nc-transcript-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35338778	ACGCCCGGCAGCAGA[A/G]CACTGGCGCGGTAAG	10043
rs764612464	in-del	-/CT			intron-variant	TOM1	GRCh38.p7	22:35326372	CCACAGCATAAGATC[-/CT]TATACCAATGGCCTT	10043
rs764646034	snp	C/G			intron-variant	TOM1	GRCh38.p7	22:35302073	CTTCTTACCTTGAAG[C/G]GTTGCCTTTCTTGGG	10043
rs764750596	snp	C/T	8.56318e-05	0.00654283	intron-variant, nc-transcript-variant	TOM1	GRCh38.p7	22:35323004	TCTGACCAAGGTGCT[C/T]GACGGCACCTCTCGG	10043
rs764801875	snp	A/G			downstream-variant-500B	TOM1	GRCh38.p7	22:35348444	AAAGTGAGCGTCCTC[A/G]ATGTATAGATGCGGA	10043
rs764854897	in-del	-/A			intron-variant	TOM1	GRCh38.p7	22:35327721	GGTACAGAGTAAAGC[-/A]ACCCAGTAAGGGGTC	10043
rs764946156	snp	A/C/T	3.65439e-05	0.00427444	intron-variant	TOM1	GRCh38.p7	22:35327406	AGCAGGTGGCACCAC[A/C/T]CCCTGGGGCTCAGAT	10043
rs764985875	snp	C/G/T	3.29768e-05	0.00406048	intron-variant	TOM1	GRCh38.p7	22:35345715	CCTTACCCTCTGCCC[C/G/T]TCCTTCCAGATCCCA	10043
rs764988880	snp	C/T	1.64974e-05	0.00287201	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334437	CAGCTCACTGGCTGA[C/T]CAACGGAAAGAGTGA	10043
rs765005954	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35322616	AAGGCAATTCCTGCA[A/G]TGGGAAGTGGAGAGT	10043
rs765038615	snp	C/T	1.65037e-05	0.00287256	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334329	TTCTGTCCCTGCAGA[C/T]CTGGGCTCCAGCAGT	10043
rs765069473	snp	A/G	1.7224e-05	0.00293457	utr-variant-3-prime, nc-transcript-variant	TOM1	GRCh38.p7	22:35347212	GTTTGCCTTATGAGT[A/G]TGGGGTCTGGCACCC	10043
rs765094252	snp	A/G			upstream-variant-2KB	TOM1	GRCh38.p7	22:35298579	GCTGGGACTACAGGC[A/G]TGTACCACCACACCT	10043
rs765095657	snp	A/T			intron-variant	TOM1	GRCh38.p7	22:35315568	TCTGTCTCTCAGCCC[A/T]GTCAGAGGAGCTTTC	10043
rs765314928	snp	C/T			missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35347142	AGGGGCCCCCGGGTC[C/T]CCCATCTGGCCCAGC	10043
rs765345756	snp	G/T	1.64757e-05	0.00287012	synonymous-codon, nc-transcript-variant, intron-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35321959	TCTTGTCCTCCTTAG[G/T]CCCAAAGATGCCCTC	10043
rs765356262	snp	G/T	3.36661e-05	0.00410267	intron-variant	TOM1	GRCh38.p7	22:35346890	CTGACCGTACTGGGG[G/T]CCCGGCTAACCTCTG	10043
rs765414001	snp	C/T	1.68801e-05	0.00290512	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35330479	TTCCTGCGCCATGAA[C/T]GGTAGCCCCAGCACC	10043
rs765443157	snp	C/T			intron-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35337182	ACCTCGTGATCCGCG[C/T]GCCTTGGCCTCCCAA	10043
rs765470183	snp	C/T	1.6577e-05	0.00287893	intron-variant	TOM1	GRCh38.p7	22:35323479	GTTACCGGCTGTGTC[C/T]CCTTGTCCCCTCTCA	10043
rs765491777	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35340320	AAGCTCTATGGGTAT[A/G]TAGCAGGGACCAGAG	10043
rs765516607	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35344432	GCTCAGGCTGTTTCC[A/G]GGTTGGCCCGGCCAG	10043
rs765590148	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35322915	ACTCCAGGAAGTCCC[A/G]TCTCCTCTCCCGGGC	10043
rs765648616	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35331181	GCTCACTGCAGCCTC[A/G]ACCTCCTGGGCTCAA	10043
rs765662954	snp	A/G	1.64732e-05	0.0028699	intron-variant	TOM1	GRCh38.p7	22:35332954	TCTCAGTCTGTCTCC[A/G]TAACTCGTGTCTTTT	10043
rs765670611	snp	C/T	1.648e-05	0.0028705	missense, intron-variant, nc-transcript-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35323550	GGTGTGGTCACCATC[C/T]ATGAGGACCTGCGGA	10043
rs765723000	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35320369	TACCTGTATAGGGCC[A/G]AGGGTGGAGGATGGT	10043
rs765762993	snp	C/T	8.7127e-05	0.00659969	missense, nc-transcript-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35338766	CTGGAGCCCTGGACG[C/T]CCGGCAGCAGAGCAC	10043
rs765811779	snp	C/G			intron-variant	TOM1	GRCh38.p7	22:35332697	ATTTTCTTTGCTGTT[C/G]TAACCTATTCCTGTT	10043
rs765833083	snp	A/G	1.64757e-05	0.00287012	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35327284	AGATTGGGAAGCTGC[A/G]CAGTGAGCTGGAGAT	10043
rs765945607	snp	G/T			intron-variant, downstream-variant-500B	TOM1, MIR3909	GRCh38.p7	22:35335908	CTAGGAACAGCATGT[G/T]CAAAGTCTCAGAGGC	10043
rs765949592	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35322770	GCATTGGGATTCTGC[A/G]TGCACTGACGCCAGT	10043
rs766004651	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35324002	AGAATTTACCATCCA[C/T]GGAGCCTCCACTTCT	10043
rs766014012	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35326290	AAATAAATCTTAGAA[A/G]CTTTCAGACTGATCT	10043
rs766028977	snp	A/G			utr-variant-3-prime, nc-transcript-variant	TOM1	GRCh38.p7	22:35347381	GGGTGTGGAGGCAGT[A/G]GGATGAACTGGGGGA	10043
rs766089484	in-del	-/GTT			intron-variant	TOM1	GRCh38.p7	22:35317231	TGGAGTTTCGCTCTC[-/GTT]GTCCAGGCTGGAGTG	10043
rs766105155	snp	A/C/T			intron-variant	TOM1	GRCh38.p7	22:35343905	CACACCTGCACACAC[A/C/T]CCCCTACACACACCA	10043
rs766114081	snp	C/T	3.29755e-05	0.00406038	intron-variant	TOM1	GRCh38.p7	22:35317862	ATGACTTTATGACTC[C/T]TGGTTTCTTCTCAGA	10043
rs766117781	snp	C/G			intron-variant	TOM1	GRCh38.p7	22:35316358	GGCACAAAATTTCCT[C/G]TGTGCACGTGGTTGA	10043
rs766125707	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35313570	TTATCCTGATTTTAC[A/G]GGTGCAAAAACAGAG	10043
rs766180887	in-del	-/A			intron-variant	TOM1	GRCh38.p7	22:35326817	TCTAGGAGGAGAGAG[-/A]GGGGGGGATCCCAGT	10043
rs766211743	in-del	-/TT			intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35335031	CCTGTGCACCGTGCA[-/TT]TTCAGGGGGTACTTT	10043
rs766300009	snp	A/G	0.000158215	0.00889284	intron-variant	TOM1	GRCh38.p7	22:35322992	CACCTCCTCTCCTCT[A/G]ACCAAGGTGCTCGAC	10043
rs766313056	snp	A/T	1.64969e-05	0.00287196	intron-variant	TOM1	GRCh38.p7	22:35317984	CCCCCCAAGGAGAGG[A/T]TGGGGGCAGAGACGG	10043
rs766329661	snp	C/G	1.69916e-05	0.00291471	intron-variant	TOM1	GRCh38.p7	22:35333514	TAAGTGTGGTTTGGA[C/G]GGCTCCAGCTGAGGG	10043
rs766363490	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35306928	TACTTGGAAATTAAG[A/G]CCTTTGCCTTCCCCT	10043
rs766430605	snp	C/T	1.69304e-05	0.00290945	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35323787	TGTTCAACTCAGAGA[C/T]ACAATCAGGACAGGA	10043
rs766463159	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35311012	TTTGATCTGGGCTTA[A/G]GAGCACGAGTTGAGG	10043
rs766466851	snp	C/T			intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35335238	AGCTAAGGAAAGTTC[C/T]AGATTATGGGATCTT	10043
rs766507715	snp	A/G	8.24463e-05	0.00642	intron-variant	TOM1	GRCh38.p7	22:35323650	GAGAACTGCCGTACC[A/G]GGAACCAAGGGAAGG	10043
rs766518538	snp	C/T	1.66921e-05	0.00288891	intron-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35321801	TGCTAAGCAATGGGC[C/T]AGGAAGATTCTGATG	10043
rs766541001	snp	C/T	1.64838e-05	0.00287083	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35345732	CCTTCCAGATCCCAG[C/T]CACCCAGGCCTGCCT	10043
rs766547379	snp	C/G			upstream-variant-2KB	TOM1	GRCh38.p7	22:35297366	AGCCTGGGTGACAGA[C/G]ACTCTGTCTTTAAAA	10043
rs766562689	snp	C/G			intron-variant	TOM1	GRCh38.p7	22:35319771	AGGGACGGGCGAGGG[C/G]CTGCCCAGGGAGGCA	10043
rs766596608	snp	C/T			upstream-variant-2KB	TOM1	GRCh38.p7	22:35298799	TTCAGATTTAAAAAC[C/T]ACAAACATCACAATA	10043
rs766620280	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35304454	TATTCTCTGCAGACA[A/G]ATCTTACTGGATCTG	10043
rs766709130	snp	C/G	1.65184e-05	0.00287384	intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334322	GTGGCCTTTCTGTCC[C/G]TGCAGACCTGGGCTC	10043
rs766794578	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35317375	TTTGTAGTTAGTAAA[A/G]ACGGGGCTTCACCAT	10043
rs766804156	snp	A/G	0.000181577	0.00952656	intron-variant	TOM1	GRCh38.p7	22:35345792	CTGACGTGGTATGTT[A/G]GGGCCCACTCCTCAC	10043
rs766810565	snp	C/G	1.64738e-05	0.00286995	intron-variant	TOM1	GRCh38.p7	22:35332930	TGCCTGGCCGTGTGT[C/G]GGGGCCTGTCTCAGT	10043
rs766866249	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35310099	ACAGGTAAATGTGGC[A/G]TGTGGGTTCCCACAC	10043
rs766891991	snp	C/T	3.33957e-05	0.00408616	splice-donor-variant	TOM1	GRCh38.p7	22:35323179	TCAACCTCATCCAGG[C/T]GAGTGCCAGGACAGG	10043
rs766956377	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35333345	GCCACAGTGCTTGGG[A/G]CAGAAAGGAACGAAG	10043
rs766975330	snp	C/T	1.65157e-05	0.0028736	intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334467	AGTGGCCTGGCCCTG[C/T]CCTGGTCCCCTGCAG	10043
rs766980335	snp	A/C			intron-variant	TOM1	GRCh38.p7	22:35321525	CGCCTCAACCTCCCA[A/C]GTAGCTGGGATTACA	10043
rs767077865	snp	G/T	0.000141383	0.00840663	intron-variant, splice-donor-variant	TOM1	GRCh38.p7	22:35299982	GGGACAGCGCATCGG[G/T]GAGTCCCTGGAGCCC	10043
rs767090065	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35313674	CTCCATGAGGGGCAG[A/G]TGGGTCTTGCCATCA	10043
rs767143772	snp	A/G			utr-variant-3-prime, nc-transcript-variant	TOM1	GRCh38.p7	22:35347406	GGGGGACAGGTCTGC[A/G]CTGCAGTGGGATCTG	10043
rs767149026	snp	A/T			intron-variant	TOM1	GRCh38.p7	22:35344468	CTTCCGCAGCTCCTC[A/T]GTGCCCGGTTCCTGC	10043
rs767248629	snp	G/T	1.81688e-05	0.00301398	intron-variant	TOM1	GRCh38.p7	22:35322981	GGGGTTCTGAGCACC[G/T]CCTCTCCTCTGACCA	10043
rs767254512	in-del	-/TT			intron-variant	TOM1	GRCh38.p7	22:35308994	TGGGTCTGGAAAGAG[-/TT]ATTCCTTTGGAAAAT	10043
rs767275153	snp	C/T	0.000133496	0.00816885	intron-variant	TOM1	GRCh38.p7	22:35346983	AGGTAGTAGTCCCCG[C/T]CCCTGCCCGCCCTCT	10043
rs767289389	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35314328	CGTTTAGGCCACATA[C/T]CCCCTCCCACCCCGC	10043
rs767383893	snp	C/G			missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35333419	GCCCCAAGTGAGGCC[C/G]AGCCGGCAGCTGACC	10043
rs767441363	snp	C/T	6.59131e-05	0.0057404	intron-variant	TOM1	GRCh38.p7	22:35327251	TGGCTTCTCTCACCA[C/T]GATCAACTGTGTGTT	10043
rs767473057	snp	A/G			intron-variant, downstream-variant-500B	TOM1, MIR3909	GRCh38.p7	22:35336140	CTGAGCACAGCTGAA[A/G]TGACATCATGCACCT	10043
rs767539597	snp	A/G	0.000148296	0.00860964	missense, intron-variant, nc-transcript-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35323578	GGAGGAAAGGCCTGG[A/G]GTTCCCCATGACTGA	10043
rs767589256	snp	C/G	8.30834e-05	0.00644475	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35333480	CCGGCAACCTCTCAT[C/G]CCAGCTGGCAGGAAT	10043
rs767599715	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35300107	GCGTGTAGCTCTCCG[A/G]CCTGGCTCCGCCCAG	10043
rs767625095	snp	A/G	0.000148379	0.00861205	intron-variant	TOM1	GRCh38.p7	22:35323645	GGTGAGAGAACTGCC[A/G]TACCGGGAACCAAGG	10043
rs767638948	snp	C/G	1.6859e-05	0.00290331	intron-variant	TOM1	GRCh38.p7	22:35333370	ACGAAGCTGCAGACA[C/G]CGGGGATGATCAGGG	10043
rs767696347	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35317580	TCAGGAATAAGCACA[C/T]GGAGGCCCACCTAGA	10043
rs767803073	snp	C/T	0.000282446	0.0118804	intron-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35321784	CACAGGTTGTGAGTC[C/T]CTGCTAAGCAATGGG	10043
rs767820552	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35314881	GTGCTTCAGTTTCCT[C/T]ATGAGATGAGGGCAA	10043
rs767859246	snp	C/T	6.66023e-05	0.00577033	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35347091	AACGGGCCAAAGCCG[C/T]GGACCGATTGCCCAA	10043
rs767869030	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35311140	CTGGTGAGTGGGAGT[A/G]GGAGGAAGGACTGGG	10043
rs768045111	snp	G/T	4.9525e-05	0.00497595	synonymous-codon, nc-transcript-variant	TOM1	GRCh38.p7	22:35345784	GCTGTCCACTGACGT[G/T]GTATGTTGGGGCCCA	10043
rs768151455	snp	C/G	5.39767e-05	0.00519475	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35338788	GCAGAGCACTGGCGC[C/G]GTAAGCAGAGGGGCC	10043
rs768164153	snp	G/T			intron-variant	TOM1	GRCh38.p7	22:35310209	ATCAGAGTGGAGTGG[G/T]CACAGGTCCTGAGGA	10043
rs768189049	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35328276	AAAGAGAGAAGACTG[C/T]GCAGGCAGCCTCGCA	10043
rs768244234	snp	C/G	1.66062e-05	0.00288146	intron-variant	TOM1	GRCh38.p7	22:35323461	GCTCACAGGTGAGCT[C/G]TGGTTACCGGCTGTG	10043
rs768252788	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35316820	ACCACCACTTGCTGA[A/G]TGTTTATTTTGGGCC	10043
rs768268121	in-del	-/A	1.64795e-05	0.00287045	frameshift-variant, intron-variant, nc-transcript-variant	TOM1	GRCh38.p7	22:35323608	CCTGGACATGCTGTC[-/A]ACCCATCCACACACC	10043
rs768289372	snp	G/T	0.00013815	0.00830999	intron-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35338666	TCCGTTCTTGCATCA[G/T]CCATCGGTAAGGGCA	10043
rs768363961	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35305550	CTGTAGTCCCAGCAA[C/T]TTGGGAGGCTGAGGC	10043
rs768369114	snp	A/C			intron-variant	TOM1	GRCh38.p7	22:35310628	GCTAGTAAGGGATCA[A/C]TGAGTGCCCAAGTGT	10043
rs768517941	snp	A/G	1.64768e-05	0.00287021	missense, nc-transcript-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35317942	GAGATCTGCGACATC[A/G]TCAACGAGACGGAGG	10043
rs768543066	snp	A/G	1.65296e-05	0.00287481	intron-variant	TOM1	GRCh38.p7	22:35317838	AGTTTACCCATTCAG[A/G]ACCCCCTCATGACTT	10043
rs768549662	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35320925	AGTTCCGGGCTACAG[C/T]GAGCTGTGATTGCAC	10043
rs768555345	snp	C/T	0.000172013	0.00927238	intron-variant	TOM1	GRCh38.p7	22:35330312	CCTCACTCTGAGTCA[C/T]GTGACTGTGGTTGCC	10043
rs768566232	in-del	-/AAGG			upstream-variant-2KB	TOM1	GRCh38.p7	22:35297897	CTTGTTAAAAGCTTA[-/AAGG]AAGGGCCAGAGATGG	10043
rs768571603	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35345111	GCCCATGTCTTTGTG[A/G]CCGAAAGTGAAATGT	10043
rs768709290	snp	C/G			intron-variant	TOM1	GRCh38.p7	22:35318870	ATCATCCAGCTCTCC[C/G]GCGGCCAGTGCAGGG	10043
rs768760110	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35345986	GGCACAGTAGCCTCT[C/T]GGCTGCTTCCCAGAG	10043
rs768792079	snp	A/C			intron-variant	TOM1	GRCh38.p7	22:35346567	CCCCTTGTGACCCTC[A/C]AAGGAAAGGAACCAG	10043
rs768792996	snp	A/G/T	5.67149e-05	0.00532492	intron-variant	TOM1	GRCh38.p7	22:35322968	AGCCACGAGGGTGGG[A/G/T]GTTCTGAGCACCTCC	10043
rs768862150	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35332583	GCACTGAAGAGAGCA[C/T]TAACACACACACACA	10043
rs768878996	snp	C/T	1.67528e-05	0.00289415	intron-variant, nc-transcript-variant	TOM1	GRCh38.p7	22:35323020	GACGGCACCTCTCGG[C/T]CCTCCAGGTCTTAGA	10043
rs768889913	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35305521	AAAAATTAGCTGGAC[A/G]TGGTGGCACACGCCT	10043
rs768910426	snp	A/C	1.65707e-05	0.00287838	synonymous-codon, nc-transcript-variant	TOM1	GRCh38.p7	22:35327354	GGAGCTGGTGCCCAC[A/C]CAGGCCGAGCCCGCA	10043
rs768952976	snp	C/T	1.66504e-05	0.0028853	intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334291	TCACACACAAGCTTG[C/T]GGATGGGTCTTTCAC	10043
rs769044619	snp	G/T	1.70156e-05	0.00291677	intron-variant	TOM1	GRCh38.p7	22:35323756	TCACTGATCCTGTTT[G/T]CCTCCCACTAGACCG	10043
rs769067919	snp	C/T	1.66391e-05	0.00288431	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35347159	CCATCTGGCCCAGCG[C/T]CCCGGAAGAAGACCC	10043
rs769071685	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35325494	TATACATTTCTGTTA[C/T]GTTAGGATTGGAGAC	10043
rs769082710	in-del	-/ATACACACA			intron-variant	TOM1	GRCh38.p7	22:35332606	CACACACACACACAC[-/ATACACACA]CACAAATATGTAATT	10043
rs769149011	snp	C/T	1.65949e-05	0.00288048	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35333459	TGGGCCCTGACCCAG[C/T]AGCCACCGGCAACCT	10043
rs769210403	snp	C/G			intron-variant	TOM1	GRCh38.p7	22:35314276	AGATCTGCCTTGTCC[C/G]GATTTTGTCTCCTCC	10043
rs769272978	snp	A/C			intron-variant	TOM1	GRCh38.p7	22:35307496	CAGCTTAGTCTCCGC[A/C]TCAGAAGAGCTGGGT	10043
rs769273959	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35330308	ACGGCCTCACTCTGA[A/G]TCATGTGACTGTGGT	10043
rs769328967	snp	C/G			intron-variant	TOM1	GRCh38.p7	22:35318476	CTGGCGTTTGCCGGG[C/G]GTTTCTGGTGTTGGG	10043
rs769388553	snp	G/T	0.000148926	0.00862792	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35330438	CAGAGGAGCTGCTCA[G/T]CGTCAATGACAATCT	10043
rs769411764	snp	A/G	3.38621e-05	0.0041146	intron-variant	TOM1	GRCh38.p7	22:35323218	CGGCCAGGAAGAGCT[A/G]TCAGTGCAGGAGCTT	10043
rs769418766	snp	C/T	1.72107e-05	0.00293343	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35323868	CCCCTCTGCCCGCCC[C/T]GCCCATACTCTCCGG	10043
rs769436491	snp	A/C			intron-variant	TOM1	GRCh38.p7	22:35318451	AGCTGAACCGTGAGC[A/C]TGAACAGCACTGGCG	10043
rs769558187	snp	C/T	4.70854e-05	0.00485185	intron-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35321845	GCTGGATACACAAAA[C/T]AGGTGGGGCACAGGG	10043
rs769558856	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35327079	CTGTGAGGGGTCTGT[A/G]GAAGGGGTGGGGCAG	10043
rs769603757	snp	C/T	0.000127089	0.00797047	intron-variant, synonymous-codon, nc-transcript-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35299958	GGGGAACCCGTTCAG[C/T]TCTCCAGTGGGACAG	10043
rs769606600	snp	C/T	0.454339	0.144033	intron-variant	TOM1	GRCh38.p7	22:35331286	TCTTTTTTTTTTTTT[C/T]TTTTTGCAGAGACAG	10043
rs769684397	snp	G/T			intron-variant	TOM1	GRCh38.p7	22:35311390	GCAAGAAGCCTGAAG[G/T]TTGGCAGTTTCAGGG	10043
rs769706359	snp	A/C	5.28471e-05	0.00514011	missense, nc-transcript-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35338733	AATACGAAGCCCCCC[A/C]AGCAACAGACGGCCT	10043
rs769712479	snp	C/T			intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35333915	GGCCATTGTCACTGT[C/T]ATCACTGTGATAGGT	10043
rs769856847	in-del	-/C			intron-variant	TOM1	GRCh38.p7	22:35325160	TGTACACACATCAGG[-/C]CCATCACATCCGCGG	10043
rs769919041	snp	C/T			intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334935	CAAGTCTTTTTCTGT[C/T]GTTCCATAGCCACCG	10043
rs770093989	snp	C/T	1.67091e-05	0.00289038	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35347066	CTAGAATTTGACAAA[C/T]TCCTGGAAGAACGGG	10043
rs770097884	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35325219	TGGTGAGTTAGACAC[A/G]GATGTGTGATGGAAA	10043
rs770203680	snp	A/C			intron-variant	TOM1	GRCh38.p7	22:35310859	ACAAAGAGATCGCCC[A/C]ACAGAGTTATTTTAA	10043
rs770271834	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35345507	GACCCCTGGCCCTGC[C/T]CCAGCTGCTGGGAGC	10043
rs770276203	snp	A/G	1.64827e-05	0.00287073	missense, nc-transcript-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35317961	ACGAGACGGAGGAAG[A/G]GTAAGGGCCCCCCAA	10043
rs770392419	snp	C/G			intron-variant	TOM1	GRCh38.p7	22:35319423	TCGTTGCTAAAGTGT[C/G]TCCCCCACTGGGTTG	10043
rs770405517	snp	A/C	5.10295e-05	0.00505096	intron-variant	TOM1	GRCh38.p7	22:35323738	TGATGTTCCCAGGAG[A/C]CCTCACTGATCCTGT	10043
rs770405974	snp	G/T	1.9204e-05	0.00309865	intron-variant	TOM1	GRCh38.p7	22:35322961	CAGGAGGAGCCACGA[G/T]GGTGGGGGTTCTGAG	10043
rs770417451	in-del	-/A			intron-variant	TOM1	GRCh38.p7	22:35324413	AGAGAGACCTGTTTC[-/A]AAAAAAAAAAAAAAA	10043
rs770447405	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35308882	ATTTTAGGGTTTCTC[C/T]TGTGGTTTATGGTTA	10043
rs770472814	snp	C/T	1.64814e-05	0.00287061	synonymous-codon, intron-variant, nc-transcript-variant	TOM1	GRCh38.p7	22:35323618	GCTGTCACCCATCCA[C/T]ACACCCCAGAGGGTG	10043
rs770514727	in-del	-/AAATAAAT			upstream-variant-2KB	TOM1	GRCh38.p7	22:35297380	AGACTCTGTCTTTAA[-/AAATAAAT]AAATAAATAAATCCA	10043
rs770543663	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35315787	GAAGAGGGCCCTGTC[C/T]AGTCCCGCAGAAACT	10043
rs770575858	snp	C/G			intron-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35337243	CCAGATAGTTGTTTT[C/G]AGTGAAGGGAAATCA	10043
rs770632043	snp	G/T			intron-variant	TOM1	GRCh38.p7	22:35330643	GCTGTCTTCTTCCAG[G/T]ATGTTTATGAGGGCC	10043
rs770654000	snp	A/G	3.30562e-05	0.00406534	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35330407	CTCATCCCTCAGATC[A/G]CCAATGAGCAGCTGA	10043
rs770668218	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35313755	CCCAATAGGGAGAGG[A/G]CAGACTGCTGTAAGG	10043
rs770714305	snp	A/T			intron-variant	TOM1	GRCh38.p7	22:35329506	ATGGGAACTTGTGGT[A/T]CTATCTTTGCATCTC	10043
rs770736121	in-del	-/CA			intron-variant	TOM1	GRCh38.p7	22:35343363	CACATCTACACCCAC[-/CA]CACACCTCCACACAC	10043
rs770765544	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35339124	TCACCTGAGGTCAGG[A/G]GTTCAAGACCAGCCT	10043
rs770767021	snp	A/G	1.6483e-05	0.00287076	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35345761	CTCATGGAGGACATC[A/G]AGCAGTGGCTGTCCA	10043
rs770777907	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35325569	TTTTCATGTTGAAAA[C/T]CAGTCAGGTTTACTT	10043
rs770845348	snp	A/T			intron-variant	TOM1	GRCh38.p7	22:35301192	TGATGGCGCCACTGT[A/T]CTCCAGCCTGGACGA	10043
rs770846227	snp	A/C	1.69536e-05	0.00291145	intron-variant	TOM1	GRCh38.p7	22:35330339	TGCCTCACTTCCTTT[A/C]CTGGCAGGAGCTCAA	10043
rs770877475	snp	C/G			intron-variant	TOM1	GRCh38.p7	22:35300055	CTGGGAAGCCTCCGG[C/G]TGCCTAGTCACGGAG	10043
rs770909639	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35318683	CCAGCAATAAGCCCG[A/G]GTCCCTGGAGGGAGC	10043
rs770939397	snp	C/G	1.67136e-05	0.00289076	synonymous-codon, nc-transcript-variant	TOM1	GRCh38.p7	22:35347173	GCCCCGGAAGAAGAC[C/G]CAGGAGAAAGATGAT	10043
rs770944518	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35311525	GGCAGGGTAGGCAGG[A/G]GCAGTCAGCATCGAA	10043
rs771218612	snp	C/T	7.72992e-05	0.0062164	intron-variant	TOM1	GRCh38.p7	22:35322958	ACACAGGAGGAGCCA[C/T]GAGGGTGGGGGTTCT	10043
rs771221028	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35342613	TCAGCTCTGCCTCAG[C/T]CTACCCAGGGCGCTG	10043
rs771242580	snp	A/G	0.000116489	0.00763092	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35346966	AAGGGGGTCACCAGC[A/G]AAGGTAGTAGTCCCC	10043
rs771245207	snp	A/G	1.6625e-05	0.00288309	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35346955	CGGAAGAGCCTAAGG[A/G]GGTCACCAGCGAAGG	10043
rs771257747	snp	C/G	4.94727e-05	0.00497332	missense, nc-transcript-variant, intron-variant	TOM1	GRCh38.p7	22:35322032	GAGGTGATGCTGGCT[C/G]TCACAGTGAGTGCCC	10043
rs771488933	in-del	-/AA			intron-variant	TOM1	GRCh38.p7	22:35305660	TGAGACTCAATCTCA[-/AA]AAAAAAAAAAAAACT	10043
rs771490363	snp	C/G			intron-variant	TOM1	GRCh38.p7	22:35340957	GGTTGACTCTACCAC[C/G]CAGTGGGCAACAAGA	10043
rs771498171	snp	C/T			intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35335100	GGTCTGACCCCTTGC[C/T]GGGACCTGCGGGAGA	10043
rs771548371	snp	G/T	0.000132904	0.00815071	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35333425	AGTGAGGCCGAGCCG[G/T]CAGCTGACCTGATCG	10043
rs771566490	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35339223	GTAATCCCAGCTACT[C/T]GGGAGGCTAAAGCAG	10043
rs771605480	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35310508	GCAGTGAGCCGAGAT[C/T]GTGCCACTGCACTCC	10043
rs771616676	snp	A/G			upstream-variant-2KB	TOM1	GRCh38.p7	22:35298071	AAAGAAGTTCATGCT[A/G]AACATAACTCCATAT	10043
rs771617048	snp	A/G	1.64727e-05	0.00286986	synonymous-codon, nc-transcript-variant	TOM1	GRCh38.p7	22:35333014	AGGCCAGACCACCAA[A/G]GTAAAAGTCTTCTTT	10043
rs771648997	snp	A/G	3.29745e-05	0.00406031	missense, intron-variant, nc-transcript-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35323526	TTCCGCAGCTCGCCC[A/G]ATCTGACAGGTGTGG	10043
rs771704680	snp	C/G			intron-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35338113	ATCAGCCTTGCGTGC[C/G]CTCCCAGTTCCTGCC	10043
rs771704785	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35310460	CGGGAGGCCGAGTGA[A/G]GCAGGTGAACTTCAA	10043
rs771738827	snp	A/G	1.64803e-05	0.00287052	synonymous-codon, intron-variant, nc-transcript-variant	TOM1	GRCh38.p7	22:35323609	CCTGGACATGCTGTC[A/G]CCCATCCACACACCC	10043
rs771760401	in-del	-/G			intron-variant	TOM1	GRCh38.p7	22:35311986	TCGGCTGGGCACGGT[-/G]GCTCACGCCTGTAAT	10043
rs771800465	snp	C/T	4.98434e-05	0.00499192	synonymous-codon, nc-transcript-variant	TOM1	GRCh38.p7	22:35327360	GGTGCCCACCCAGGC[C/T]GAGCCCGCAGACCTG	10043
rs771846116	snp	A/C			intron-variant	TOM1	GRCh38.p7	22:35309252	GAGGCCGAGGAGTTA[A/C]CCAGGCTCACACAGC	10043
rs771892434	snp	C/G	1.71369e-05	0.00292714	intron-variant	TOM1	GRCh38.p7	22:35330322	AGTCATGTGACTGTG[C/G]TTGCCTCACTTCCTT	10043
rs771904449	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35315419	CTCCAAAGCAGGGCA[C/T]GGCCCTCTGCTCAGA	10043
rs771972019	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35332369	CTAATTTGGGCTTCA[A/G]CACTTCAGGGAGGCA	10043
rs771978857	snp	A/G	1.656e-05	0.00287745	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35323114	GAGTGTGCTGGTGAG[A/G]ACCATCCTGCCCAAG	10043
rs771996974	snp	A/C	0.000131133	0.00809626	missense, nc-transcript-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35338764	GGCTGGAGCCCTGGA[A/C]GCCCGGCAGCAGAGC	10043
rs772018359	snp	G/T			intron-variant	TOM1	GRCh38.p7	22:35324120	AGTCATCAGAGACAG[G/T]TGGGATCCAAGCTCA	10043
rs772087164	snp	C/G	1.6607e-05	0.00288153	intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334304	TGTGGATGGGTCTTT[C/G]ACGTGGCCTTTCTGT	10043
rs772107351	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35325267	TTTCCCAATAAGCGT[C/T]CCCACTGCCCACTTT	10043
rs772160251	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35314104	TGGAATATGCCTACC[C/T]TGTGGGCATCTGAAG	10043
rs772266505	snp	A/G/T	3.30569e-05	0.00406541	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35330404	GAGCTCATCCCTCAG[A/G/T]TCGCCAATGAGCAGC	10043
rs772277453	snp	A/G			intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35335110	CTTGCCGGGACCTGC[A/G]GGAGAACTGGCCCCG	10043
rs772445751	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35307421	CCCATGAGCCCACCT[A/G]GCATGATCCCAGGTA	10043
rs772448490	snp	C/T	6.80168e-05	0.00583128	synonymous-codon, nc-transcript-variant	TOM1	GRCh38.p7	22:35323770	TTCCTCCCACTAGAC[C/T]GTGTTCAACTCAGAG	10043
rs772450038	snp	A/G	1.64789e-05	0.0028704	intron-variant	TOM1	GRCh38.p7	22:35321918	GGTGTTAGGTAAGGG[A/G]GCTCTATTCCTAAGC	10043
rs772469490	snp	A/G/T	3.33196e-05	0.00408153	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35347163	CTGGCCCAGCGCCCC[A/G/T]GAAGAAGACCCAGGA	10043
rs772489716	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35344987	AGGTCCAGCTCTTTC[C/T]CACTCTGAAGTCTGT	10043
rs772491889	snp	A/G			intron-variant, nc-transcript-variant	TOM1, MIR3909	GRCh38.p7	22:35335684	GGAGCAGGCTCCGGG[A/G]GACAGGGAAAAGCAC	10043
rs772593543	in-del	-/TG	3.29522e-05	0.00405894	intron-variant	TOM1	GRCh38.p7	22:35327259	CTCACCACGATCAAC[-/TG]TGTGTTTCAGATTGG	10043
rs772622931	snp	A/C	1.64874e-05	0.00287113	missense, nc-transcript-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334414	GACATGTTTGCGCTG[A/C]CACGGGGCAGCTCAC	10043
rs772623455	snp	A/C/T	1.65605e-05	0.0028775	intron-variant	TOM1	GRCh38.p7	22:35323486	GCTGTGTCCCCTTGT[A/C/T]CCCTCTCAGTCCTGG	10043
rs772641612	in-del	-/CA			intron-variant	TOM1	GRCh38.p7	22:35343116	TACACCACACACACC[-/CA]CACACACCACACACA	10043
rs772645605	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35318477	TGGCGTTTGCCGGGC[A/G]TTTCTGGTGTTGGGG	10043
rs772651151	in-del	-/G	1.66504e-05	0.0028853	splice-donor-variant, intron-variant	TOM1	GRCh38.p7	22:35346973	TCACCAGCGAAGGTA[-/G]TAGTCCCCGCCCCTG	10043
rs772816357	snp	A/T	1.64999e-05	0.00287222	intron-variant	TOM1	GRCh38.p7	22:35317854	ACCCCCTCATGACTT[A/T]ATGACTCCTGGTTTC	10043
rs772849873	snp	C/T	3.29451e-05	0.00405851	intron-variant	TOM1	GRCh38.p7	22:35333027	AAGGTAAAAGTCTTC[C/T]TTTCTGTGACTAGAT	10043
rs772905845	snp	A/C			intron-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35338340	TACGACCTCATACAC[A/C]ACCACAGTCTATAAA	10043
rs772912853	snp	A/G	4.94385e-05	0.0049716	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35317953	CATCATCAACGAGAC[A/G]GAGGAAGGGTAAGGG	10043
rs772938813	snp	A/G	1.64836e-05	0.0028708	missense, intron-variant, nc-transcript-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35323532	AGCTCGCCCGATCTG[A/G]CAGGTGTGGTCACCA	10043
rs772946063	snp	A/G	1.66161e-05	0.00288232	missense, nc-transcript-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35323047	TAGAAACCTGTGTCA[A/G]GAACTGCGGGCACCG	10043
rs772948986	snp	C/G			missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35323824	GGGCACTGACTCCAG[C/G]CAGCAAGAGGACTCT	10043
rs772965850	snp	A/G	1.7119e-05	0.00292562	intron-variant	TOM1	GRCh38.p7	22:35330325	CATGTGACTGTGGTT[A/G]CCTCACTTCCTTTCC	10043
rs772976479	snp	C/T			intron-variant, downstream-variant-500B	TOM1, MIR3909	GRCh38.p7	22:35335854	GAGGGTACTCAGAGC[C/T]GGACCAGGTGCTGGG	10043
rs772993868	in-del	-/T			intron-variant	TOM1	GRCh38.p7	22:35312211	ATCGCACCACTGTAC[-/T]CCAGCCTGGGCGACA	10043
rs773049759	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35328379	AGCTCCCATGCACTG[A/G]GCACTTCCCGTGTCC	10043
rs773071776	snp	A/G/T	0.000218056	0.0104398	missense, nc-transcript-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35338765	GCTGGAGCCCTGGAC[A/G/T]CCCGGCAGCAGAGCA	10043
rs773102885	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35316315	GCCAGAGTGATGTGT[A/G]TAATGGAACGTTACC	10043
rs773103141	snp	G/T			intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	TOM1	GRCh38.p7	22:35299858	CTCCGAGTGCGTCAC[G/T]TGACGGGTCGGTGGC	10043
rs773104807	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35329235	TGCTGGGATTATAGG[C/T]ACGAGCCACCGGGTG	10043
rs773159832	snp	A/T			intron-variant	TOM1	GRCh38.p7	22:35317178	TACCAACTCAAAAGA[A/T]AATTCTTTTTTGCTT	10043
rs773159993	snp	A/G	1.64977e-05	0.00287203	intron-variant	TOM1	GRCh38.p7	22:35345704	CTAGGGCACTGCCTT[A/G]CCCTCTGCCCTTCCT	10043
rs773263738	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35319484	AGCAGAGTACCGGAC[A/G]TCATGGGCCCACAGC	10043
rs773287192	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35321440	CTCTCACTCTGTTGC[C/T]CAGGCTGGAGTACAG	10043
rs773293970	snp	A/G			downstream-variant-500B	TOM1	GRCh38.p7	22:35348447	GTGAGCGTCCTCGAT[A/G]TATAGATGCGGAGAC	10043
rs773308798	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35341310	CACTTACGCTTCGCA[A/G]TACCGCCATGTCCTC	10043
rs773318728	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35346636	TGGCGTGCTGTGTGT[C/T]ATCCCATTTCAGCTT	10043
rs773398404	in-del	-/AGA	1.65332e-05	0.00287512	cds-indel, nc-transcript-variant	TOM1	GRCh38.p7	22:35330424	CAATGAGCAGCTGAC[-/AGA]GGAGCTGCTCATCGT	10043
rs773534236	snp	A/G	1.64789e-05	0.0028704	intron-variant	TOM1	GRCh38.p7	22:35321919	GTGTTAGGTAAGGGG[A/G]CTCTATTCCTAAGCC	10043
rs773560743	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35303623	CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGATTAG	10043
rs773568229	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35332747	ATGACTAAGGTTGCC[C/T]TATAATTGATCATCC	10043
rs773576583	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35304377	GAGAGGATTCCAGAT[C/T]CTTTGTACCAGCTGG	10043
rs773616991	snp	G/T			upstream-variant-2KB	TOM1	GRCh38.p7	22:35298601	ACCACACCTGGCTAA[G/T]TTTTGTATTTTTAGT	10043
rs773620607	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35311401	GAAGGTTGGCAGTTT[C/T]AGGGTGGGTTTGACA	10043
rs773623729	in-del	-/T			intron-variant	TOM1	GRCh38.p7	22:35331093	AAACACCTGTCCACC[-/T]TTTTTTTTTTTTTTT	10043
rs773722590	snp	A/G	8.08506e-05	0.00635757	intron-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35321795	AGTCCCTGCTAAGCA[A/G]TGGGCTAGGAAGATT	10043
rs773737225	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35307459	TTGATCACTGGGACG[C/T]AAGCAGCCTGAAATG	10043
rs773797571	snp	C/T			intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334023	ACTTTTTGAAAAAAT[C/T]GACTACCCATCTGAT	10043
rs773808057	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35305346	TAGGGACAGGGAAGG[A/G]TTGATGCCAGAGGGA	10043
rs773989875	snp	A/G/T	6.74018e-05	0.00580491	intron-variant	TOM1	GRCh38.p7	22:35346881	TGCCCCAGGCTGACC[A/G/T]TACTGGGGGCCCGGC	10043
rs774076895	snp	A/C			intron-variant	TOM1	GRCh38.p7	22:35314403	TGCCACTCATGGCTC[A/C]GGAGCTTGCCTGCAC	10043
rs774084309	snp	A/G	1.65993e-05	0.00288086	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35330449	CTCATCGTCAATGAC[A/G]ATCTCAACAATGTGT	10043
rs774119178	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35325599	TCAGCCTCAAAGAGC[A/G]TGTTTATGTAAAATT	10043
rs774133911	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35330698	CCTTTCCAGGGTTAG[C/T]GCTGCTGCCTGTGCC	10043
rs774304642	snp	C/T	0.00041774	0.0144463	intron-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35338671	TCTTGCATCAGCCAT[C/T]GGTAAGGGCAGCATC	10043
rs774309553	in-del	-/AAA			intron-variant	TOM1	GRCh38.p7	22:35305659	GTGAGACTCAATCTC[-/AAA]AAAAAAAAAAAAACT	10043
rs774320696	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35307608	AGCACTGCAAAGTGC[A/G]GTGGAGAACCACTGT	10043
rs774337989	snp	A/C			intron-variant	TOM1	GRCh38.p7	22:35318686	GCAATAAGCCCGAGT[A/C]CCTGGAGGGAGCAGA	10043
rs774443606	in-del	-/ACACACACA			intron-variant	TOM1	GRCh38.p7	22:35332596	CACTAACACACACAC[-/ACACACACA]CATACACACACACAA	10043
rs774638447	snp	A/G			downstream-variant-500B	TOM1	GRCh38.p7	22:35348169	ACATGGCAGGCTCCA[A/G]CCACCGCCCCTGCCC	10043
rs774644191	snp	C/T	1.66452e-05	0.00288484	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35347160	CATCTGGCCCAGCGC[C/T]CCGGAAGAAGACCCA	10043
rs774671873	snp	C/T	1.70229e-05	0.00291739	intron-variant	TOM1	GRCh38.p7	22:35323757	CACTGATCCTGTTTT[C/T]CTCCCACTAGACCGT	10043
rs774689650	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35342624	TCAGCCTACCCAGGG[C/T]GCTGGCATCCCAGAG	10043
rs774744360	snp	G/T	1.6473e-05	0.00286988	intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334299	AAGCTTGTGGATGGG[G/T]CTTTCACGTGGCCTT	10043
rs774749182	snp	C/G			intron-variant	TOM1	GRCh38.p7	22:35344246	GACTGGATGGTGAGA[C/G]AAGGCATGGTGAGCA	10043
rs774757988	snp	C/T	0.000112152	0.00748754	intron-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35321762	CTGCTGCTGGAGGTC[C/T]AGGGGCCACAGGTTG	10043
rs774759700	snp	A/G			intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334158	TGGGAAGAGGAAGCC[A/G]CTTGCCCAAGGCCCC	10043
rs774801951	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35327032	CGTGGTGGCTCATTC[C/T]GGTGTGGAGATGGTA	10043
rs774842627	snp	C/T	1.65537e-05	0.0028769	synonymous-codon, nc-transcript-variant	TOM1	GRCh38.p7	22:35330439	AGAGGAGCTGCTCAT[C/T]GTCAATGACAATCTC	10043
rs774858180	snp	A/T			intron-variant	TOM1	GRCh38.p7	22:35322427	TAAAATAAATACCAG[A/T]GGCTGAGAACAGTCT	10043
rs774899107	in-del	-/TTTGAACGGTTCCGA	1.64727e-05	0.00286986	cds-indel, nc-transcript-variant	TOM1	GRCh38.p7	22:35332981	TTTCTGTCTTGTAGG[-/TTTGAACGGTTCCGA]TTTGAACGGTTCCGA	10043
rs774929369	snp	C/T			upstream-variant-2KB	TOM1	GRCh38.p7	22:35298193	ATACCATTACTGAAA[C/T]GTAGATCTATTTAAG	10043
rs774932722	snp	C/G	1.66001e-05	0.00288094	missense, nc-transcript-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35323147	CAACCCACCCACCAT[C/G]GTGCATGACAAAGTG	10043
rs775043446	in-del	-/CA	0.000293532	0.0121111	intron-variant	TOM1	GRCh38.p7	22:35323960	TCCAGGCAGGTGGGC[-/CA]CACACGTCAGGGAGG	10043
rs775075889	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35307723	GGGAAGGACGGAGCC[A/G]GGGGAGAAGGGAGGG	10043
rs775127963	snp	C/G	2.13641e-05	0.00326827	intron-variant	TOM1	GRCh38.p7	22:35321850	ATACACAAAACAGGT[C/G]GGGCACAGGGAGGAT	10043
rs775169115	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35332871	GTCATCACCCTGATC[A/G]TAACCCACCGTGTTG	10043
rs775201856	snp	A/C			intron-variant	TOM1	GRCh38.p7	22:35328269	GGCTCCGAAAGAGAG[A/C]AGACTGCGCAGGCAG	10043
rs775273136	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35315427	CAGGGCACGGCCCTC[C/T]GCTCAGAGGGACACT	10043
rs775323622	snp	A/C			intron-variant	TOM1	GRCh38.p7	22:35339236	CTCGGGAGGCTAAAG[A/C]AGGAGAATCGCTTGA	10043
rs775424511	snp	A/G	1.6989e-05	0.00291449	intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB	TOM1	GRCh38.p7	22:35299878	GGGTCGGTGGCGCTG[A/G]CGGTTGCTGTCAGCT	10043
rs775514989	snp	C/T	3.39023e-05	0.00411704	intron-variant	TOM1	GRCh38.p7	22:35323220	GCCAGGAAGAGCTGT[C/T]AGTGCAGGAGCTTCC	10043
rs775683778	snp	A/C/G	4.9558e-05	0.00497764	intron-variant	TOM1	GRCh38.p7	22:35322053	GTGAGTGCCCCATCT[A/C/G]TCTGTCCTGTGGCAG	10043
rs775691549	snp	G/T	0.000164785	0.00907555	missense, intron-variant, nc-transcript-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35323555	GGTCACCATCTATGA[G/T]GACCTGCGGAGGAAA	10043
rs775747380	snp	C/G			intron-variant	TOM1	GRCh38.p7	22:35300104	CTGGCGTGTAGCTCT[C/G]CGACCTGGCTCCGCC	10043
rs775772069	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35322533	TGGCTGGGGAAGATA[C/T]AAATGCTGTCCCACC	10043
rs775773543	snp	A/G	5.74069e-05	0.00535725	intron-variant	TOM1	GRCh38.p7	22:35322963	GGAGGAGCCACGAGG[A/G]TGGGGGTTCTGAGCA	10043
rs775773718	snp	G/T			intron-variant	TOM1	GRCh38.p7	22:35344304	TGGGGGTGCTCGCAG[G/T]GCTCCTGCCAGGCAT	10043
rs775798856	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35325259	AGCTTAACTTTCCCA[A/G]TAAGCGTCCCCACTG	10043
rs775808746	snp	A/G	1.6601e-05	0.00288101	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35333440	GCAGCTGACCTGATC[A/G]ACATGGGCCCTGACC	10043
rs775819011	in-del	-/AC			intron-variant	TOM1	GRCh38.p7	22:35332594	AGCACTAACACACAC[-/AC]ACACACACACATACA	10043
rs775878174	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35332514	TCGATCTATCACACC[A/G]GCCCCTAAGTAGCTC	10043
rs775879864	snp	A/G	6.5937e-05	0.00574144	intron-variant	TOM1	GRCh38.p7	22:35327222	CGCTGTGAGTAACAT[A/G]GGCCCCAGAACCCTG	10043
rs775917077	snp	A/C	1.66593e-05	0.00288607	intron-variant	TOM1	GRCh38.p7	22:35346978	AGCGAAGGTAGTAGT[A/C]CCCGCCCCTGCCCGC	10043
rs775947070	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35316087	AGATAATAGACAGCC[A/G]GCAGCACTGTGCTCA	10043
rs775967499	snp	G/T	0.000135053	0.00821634	intron-variant	TOM1	GRCh38.p7	22:35321701	ACCGCGCCCGGCCAG[G/T]TTCTGCACTTTTAAC	10043
rs775987283	snp	C/T	1.64817e-05	0.00287064	missense, intron-variant, nc-transcript-variant	TOM1	GRCh38.p7	22:35323622	TCACCCATCCACACA[C/T]CCCAGAGGGTGAGAG	10043
rs775989818	snp	A/T	1.64936e-05	0.00287168	intron-variant	TOM1	GRCh38.p7	22:35345708	GGCACTGCCTTACCC[A/T]CTGCCCTTCCTTCCA	10043
rs776007349	snp	C/T	3.33868e-05	0.00408562	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35347078	AAATTCCTGGAAGAA[C/T]GGGCCAAAGCCGCGG	10043
rs776023641	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35312911	GTTATGTTTGAGTAG[A/G]GCGTGGAGGTGACAG	10043
rs776356471	snp	G/T	1.64822e-05	0.00287068	splice-donor-variant	TOM1	GRCh38.p7	22:35317962	CGAGACGGAGGAAGG[G/T]TAAGGGCCCCCCAAG	10043
rs776365405	snp	A/G	1.68371e-05	0.00290143	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35330347	TTCCTTTCCTGGCAG[A/G]AGCTCAACCGCACGT	10043
rs776393900	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35339365	TGGAGACCAGTGGCC[C/T]GGGCTTCACATTCCA	10043
rs776397225	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35306669	TCGTGTTGTTGTGCT[A/G]TAAAGCACTTCCTGC	10043
rs776441804	in-del	-/G			intron-variant	TOM1	GRCh38.p7	22:35317709	TGACGATGGGACAAT[-/G]TGTATAGAGCAGTCT	10043
rs776468986	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35340304	TTGGGGGTAGGAAGT[A/G]AAGCTCTATGGGTAT	10043
rs776473922	snp	A/T			intron-variant, upstream-variant-2KB	TOM1	GRCh38.p7	22:35299640	TAGACCTCGCCCTAA[A/T]AGGTCAGGGGCGTGG	10043
rs776502430	snp	C/G			intron-variant	TOM1	GRCh38.p7	22:35310725	CAGTCATTCAGCAAA[C/G]AGGTACTGCAGGTTT	10043
rs776530727	in-del	-/CACA			intron-variant	TOM1	GRCh38.p7	22:35343420	CAGCCCTACACACAC[-/CACA]CACACATATCTACAC	10043
rs776563626	snp	A/G	1.64846e-05	0.0028709	stop-gained, nc-transcript-variant	TOM1	GRCh38.p7	22:35345769	GGACATCGAGCAGTG[A/G]CTGTCCACTGACGTG	10043
rs776568796	snp	C/T	1.65935e-05	0.00288036	missense, nc-transcript-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35323058	GTCAAGAACTGCGGG[C/T]ACCGCTTCCACGTGC	10043
rs776600278	snp	A/G/T	8.23833e-05	0.00641764	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35327313	ATGGTGAGTGGGAAC[A/G/T]TGAGGGTGATGTCGG	10043
rs776726298	in-del	-/GAA			intron-variant	TOM1	GRCh38.p7	22:35313168	CCTGACCAACATGGT[-/GAA]GCCCCATCTCTACTA	10043
rs776768946	in-del	-/GGGCCATGAGCTGCTTGTGGA			intron-variant	TOM1	GRCh38.p7	22:35324982	TCCTCATGGCCCACT[-/GGGCCATGAGCTGCTTGTGGA]GGGCCATGAGCTGCT	10043
rs776795357	snp	A/C			intron-variant	TOM1	GRCh38.p7	22:35300072	GCCTAGTCACGGAGG[A/C]AGGGAGGGCAAGGAG	10043
rs776837055	snp	A/C	1.64787e-05	0.00287038	intron-variant	TOM1	GRCh38.p7	22:35321927	TAAGGGGGCTCTATT[A/C]CTAAGCCCACCCTTT	10043
rs776843610	snp	A/G	6.58935e-05	0.00573955	intron-variant	TOM1	GRCh38.p7	22:35332934	TGGCCGTGTGTGGGG[A/G]CCTGTCTCAGTCTGT	10043
rs776900318	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35322423	AATGTAAAATAAATA[C/T]CAGTGGCTGAGAACA	10043
rs776912039	in-del	-/T/TT	0.494793	0.119619	intron-variant	TOM1	GRCh38.p7	22:35331272	GCTAATTTTCTTTTC[-/T/TT]TTTTTTTTTTTTTCT	10043
rs776917573	snp	C/T	9.18721e-05	0.00677699	intron-variant	TOM1	GRCh38.p7	22:35323964	GGCAGGTGGGCCACA[C/T]ACGTCAGGGAGGGCC	10043
rs776931943	snp	C/T	1.65121e-05	0.00287329	intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334325	GCCTTTCTGTCCCTG[C/T]AGACCTGGGCTCCAG	10043
rs776963797	snp	A/G	1.66272e-05	0.00288328	synonymous-codon, nc-transcript-variant	TOM1	GRCh38.p7	22:35346956	GGAAGAGCCTAAGGG[A/G]GTCACCAGCGAAGGT	10043
rs776997794	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35313294	AGAGGTTGCAGTGAG[C/T]CAAGATCGTGCCACT	10043
rs777022000	snp	C/G	1.64947e-05	0.00287177	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334431	ACGGGGCAGCTCACT[C/G]GCTGACCAACGGAAA	10043
rs777040017	snp	C/G	1.68457e-05	0.00290216	intron-variant	TOM1	GRCh38.p7	22:35346886	CAGGCTGACCGTACT[C/G]GGGGCCCGGCTAACC	10043
rs777194528	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35331743	TACAAAAAAATTAGC[C/T]GGAGGTGGTGGTGGG	10043
rs777198340	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35345149	TGTAGCACCGCCCCT[C/T]TGGGTCTACCCACCT	10043
rs777306500	snp	C/T	1.7903e-05	0.00299185	intron-variant	TOM1	GRCh38.p7	22:35333545	TACATTATGGTACTG[C/T]GGGCACCCCTGCAGA	10043
rs777332465	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35308844	AACATTGTGGGTTGC[A/G]GAAGCAATACCCTCT	10043
rs777337863	snp	C/T	1.6748e-05	0.00289374	intron-variant	TOM1	GRCh38.p7	22:35347032	GCCTCAGGGCCTACC[C/T]TCACCCTCTCCCCTT	10043
rs777342341	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35304464	AGACAAATCTTACTG[A/G]ATCTGTTTTGTTTTT	10043
rs777365636	snp	A/C			intron-variant	TOM1	GRCh38.p7	22:35344916	AGGACGAGGGAAATC[A/C]GGCGCAGAGAAGTTA	10043
rs777394466	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35319236	TTGGGGACAGCAAGC[C/T]CCCATGTCCCTTATA	10043
rs777396894	snp	C/G	1.64972e-05	0.00287199	intron-variant	TOM1	GRCh38.p7	22:35323675	GGAAGGGAGGCAGGA[C/G]TCATCCCCAGAGACA	10043
rs777404484	snp	A/G	3.29652e-05	0.00405974	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35345758	TGCCTCATGGAGGAC[A/G]TCGAGCAGTGGCTGT	10043
rs777439333	snp	G/T			intron-variant	TOM1	GRCh38.p7	22:35320436	CCCCAGCTTCCAGGG[G/T]CCTCCCAACACCGTG	10043
rs777439847	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35313745	CTGCACCAGACCCAA[C/T]AGGGAGAGGACAGAC	10043
rs777657300	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35302621	ACAGGCATGACCACC[A/G]TGTCCGGCCTAGAAT	10043
rs777659743	snp	A/C/G	0.000140496	0.00838038	intron-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35321837	AGAACCTGGCTGGAT[A/C/G]CACAAAACAGGTGGG	10043
rs777760954	snp	C/T	1.66763e-05	0.00288753	intron-variant, utr-variant-5-prime, nc-transcript-variant	TOM1	GRCh38.p7	22:35299924	TGGCAGCGGCGGTAG[C/T]AGCAATGGACTTTCT	10043
rs777923674	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35302955	CTGTAAACCAGGCCC[C/T]TCCTTGCTGCAGGAG	10043
rs777971421	snp	A/G			intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35335537	GCTAATGAGTGTGAT[A/G]GGACTTGCAGCCAGA	10043
rs777983804	snp	A/C	8.75235e-05	0.00661469	intron-variant	TOM1	GRCh38.p7	22:35330524	GCCTACTGCCCCAAC[A/C]CTCTCCCTTCCCTTC	10043
rs778069270	snp	A/G	1.65605e-05	0.0028775	missense, nc-transcript-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35323115	AGTGTGCTGGTGAGG[A/G]CCATCCTGCCCAAGA	10043
rs778086504	snp	C/G			upstream-variant-2KB	TOM1	GRCh38.p7	22:35299096	TTTTTCTTCAGAAAG[C/G]CTCATGGCTTTTGTC	10043
rs778128686	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35312213	CGCACCACTGTACTC[C/T]AGCCTGGGCGACAGA	10043
rs778136300	snp	A/T			intron-variant	TOM1	GRCh38.p7	22:35341636	TCCCAGCCAATCTGC[A/T]CCTGCTGCAGCCCAG	10043
rs778165256	snp	C/T	1.83118e-05	0.00302582	intron-variant	TOM1	GRCh38.p7	22:35323955	TCAGGTCCAGGCAGG[C/T]GGGCCACACACGTCA	10043
rs778168261	snp	C/T	1.64879e-05	0.00287118	synonymous-codon, nc-transcript-variant, intron-variant	TOM1	GRCh38.p7	22:35322026	TTCCACGAGGTGATG[C/T]TGGCTCTCACAGTGA	10043
rs778212717	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35328052	CCATGAGGAGACAGA[A/G]CGCTTCGTGTAACTG	10043
rs778249286	snp	C/G	8.42496e-05	0.00648981	missense, nc-transcript-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35338713	TGGTCTCTCTTTCAG[C/G]GTAAAATACGAAGCC	10043
rs778280836	snp	A/C			utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B	TOM1	GRCh38.p7	22:35347975	AAGGTAGAAAACCAC[A/C]CTGCTAGCAGCATTG	10043
rs778334914	snp	C/T	8.82729e-05	0.00664294	intron-variant	TOM1	GRCh38.p7	22:35300008	AGCCCCCCACAGCTC[C/T]GCCCCGGTGCTCCGC	10043
rs778359761	snp	G/T			intron-variant	TOM1	GRCh38.p7	22:35338897	CCCAGCACGTCCACA[G/T]GCCCTTCCTCGTTTG	10043
rs778361543	snp	G/T	3.30967e-05	0.00406783	intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334499	TCGGGTGGCTCTCGG[G/T]GTTCTGGAACCCGGT	10043
rs778361846	snp	G/T			intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334169	AGCCGCTTGCCCAAG[G/T]CCCCACAGCCAGCAG	10043
rs778407440	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35310442	CCTGTAGTCCCAGCT[A/G]CTCGGGAGGCCGAGT	10043
rs778408858	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35315940	CTTACAAATAGCCGT[A/G]TAGCAAGCGAAGAGT	10043
rs778408859	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35328721	CTGACCTTGGAGGGG[A/G]CAGGGGACAGGGTCC	10043
rs778456902	snp	C/G/T	3.32531e-05	0.00407746	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35346954	GCGGAAGAGCCTAAG[C/G/T]GGGTCACCAGCGAAG	10043
rs778456974	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35340843	CAAGGGCACTCTCTC[C/T]GCTCCTGGGTCTCCC	10043
rs778459644	snp	C/T	1.67253e-05	0.00289178	intron-variant	TOM1	GRCh38.p7	22:35347006	CGCCCTCTCCTTTCC[C/T]CAGGGCTCTGGCCTC	10043
rs778460156	snp	C/G			intron-variant	TOM1	GRCh38.p7	22:35316594	GGTCCCGGCCATGGC[C/G]CTGACAGGCTTCCAG	10043
rs778472244	in-del	-/ACACACACAT			intron-variant	TOM1	GRCh38.p7	22:35332597	CTAACACACACACAC[-/ACACACACAT]ACACACACATACACA	10043
rs778513783	in-del	-/CA			intron-variant	TOM1	GRCh38.p7	22:35342907	CACATCTACACCCAC[-/CA]CACACACCTCCACAC	10043
rs778522375	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35314754	GAAAACAGTGTTCCC[C/T]GCCCCTGCTGAGAGA	10043
rs778523295	in-del	-/C	4.36138e-05	0.00466958	frameshift-variant, nc-transcript-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35338757	ACGGCCTGGCTGGAG[-/C]CCTGGACGCCCGGCA	10043
rs778537779	snp	G/T	1.6473e-05	0.00286988	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35333001	AACGGTTCCGAACAG[G/T]CCAGACCACCAAGGT	10043
rs778540391	snp	G/T	1.94158e-05	0.00311569	intron-variant	TOM1	GRCh38.p7	22:35322952	TCTGGGACACAGGAG[G/T]AGCCACGAGGGTGGG	10043
rs778592532	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35339162	ATGGTGAAACCCCGT[A/G]TCTACTAAAAATACA	10043
rs778601750	snp	G/T			intron-variant	TOM1	GRCh38.p7	22:35311198	CTTCAGTGGAGCCCG[G/T]TGCCTTCAGGTCCAT	10043
rs778629719	snp	C/T	1.66189e-05	0.00288256	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35333423	CAAGTGAGGCCGAGC[C/T]GGCAGCTGACCTGAT	10043
rs778750737	snp	A/C/T	3.30143e-05	0.00406279			GRCh38.p7	22:35345688	TCTTCCACCTTGTCA[A/C/T]CTAGGGCACTGCCTT	10043
rs778761682	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35319473	TTTGTGCTCCCAGCA[A/G]AGTACCGGACATCAT	10043
rs778809680	snp	A/G	1.64904e-05	0.00287139	intron-variant	TOM1	GRCh38.p7	22:35323661	TACCGGGAACCAAGG[A/G]AAGGGAGGCAGGACT	10043
rs778815300	snp	A/G	0.00016509	0.00908393	intron-variant	TOM1	GRCh38.p7	22:35317998	GTTGGGGGCAGAGAC[A/G]GCCATCCCACCACGC	10043
rs778820960	snp	A/G	4.96841e-05	0.00498393	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35330381	GAGCCATGCAGCAGC[A/G]GGTCCTGGAGCTCAT	10043
rs778870921	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35324025	CCACTTCTTCCTCAC[A/G]GCAGCCCACAGGGTA	10043
rs778894485	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35309424	CAAGACAGGCAGATC[A/G]CCTGAGGTCAGGAGT	10043
rs778898133	snp	A/G			intron-variant, downstream-variant-500B	TOM1, MIR6069	GRCh38.p7	22:35336717	AGCCCCTGCCCACCA[A/G]CCCCACTGGGACCAC	10043
rs778916681	snp	G/T	1.65614e-05	0.00287757	missense, nc-transcript-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35323109	GTGGAGAGTGTGCTG[G/T]TGAGGACCATCCTGC	10043
rs778923802	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35321559	TCATACCACCACGCC[C/T]GGCAAATTTTTGTAT	10043
rs778960919	in-del	-/G			intron-variant	TOM1	GRCh38.p7	22:35310958	AGGCCCTGGCGGGGT[-/G]GGGGGGTGTCAGGGC	10043
rs779003638	snp	C/T	1.71566e-05	0.00292883	intron-variant	TOM1	GRCh38.p7	22:35333524	TTGGAGGGCTCCAGC[C/T]GAGGGTACATTATGG	10043
rs779062832	in-del	-/C			intron-variant	TOM1	GRCh38.p7	22:35319844	TTGGTGGGCCACCAT[-/C]CCTTTCCCCACCGTG	10043
rs779124879	snp	A/G	4.94466e-05	0.00497201	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35345738	AGATCCCAGTCACCC[A/G]GGCCTGCCTCATGGA	10043
rs779134594	in-del	-/AC			intron-variant	TOM1	GRCh38.p7	22:35343398	TCCACTCATAAACCT[-/AC]ACACACAGCCCTACA	10043
rs779207585	snp	A/G	1.65304e-05	0.00287488	intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334486	GGTCCCCTGCAGTTC[A/G]GGTGGCTCTCGGGGT	10043
rs779235123	snp	G/T			intron-variant	TOM1	GRCh38.p7	22:35313909	AGCTGCTACCCGGAG[G/T]CCCTTGAAGGTTACA	10043
rs779259622	snp	C/T			intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35333855	CTCGTGTATGAGAAG[C/T]GCTTAGACCATGCCA	10043
rs779296524	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35330081	TCAGGAGATCGAGAC[C/T]ACCCTGGCTAATATG	10043
rs779311008	snp	C/T	3.55088e-05	0.00421345	utr-variant-3-prime, nc-transcript-variant	TOM1	GRCh38.p7	22:35347245	CAGCCCAGGTCCCCA[C/T]TGCTCTCACACCCTT	10043
rs779371557	snp	A/T	0.000195103	0.00987489	intron-variant, utr-variant-5-prime, nc-transcript-variant	TOM1	GRCh38.p7	22:35299909	GATTCCCGGGGTTGG[A/T]GGCAGCGGCGGTAGC	10043
rs779377961	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35316807	TTTAAAAAGAACCAC[C/T]ACCACTTGCTGAGTG	10043
rs779421266	snp	A/G			intron-variant, nc-transcript-variant	TOM1, MIR3909	GRCh38.p7	22:35335674	CTTCCTCTGGGGAGC[A/G]GGCTCCGGGGGACAG	10043
rs779430094	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35306542	GAATGGTCTGAGTCC[C/T]GGTTCAGTCCTCAAC	10043
rs779441456	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35317977	GTAAGGGCCCCCCAA[A/G]GAGAGGTTGGGGGCA	10043
rs779445069	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35311861	TGGCTGTCATTGTTC[C/T]CCATGATGTTGTTAT	10043
rs779477487	snp	A/G	1.6795e-05	0.0028978	intron-variant	TOM1	GRCh38.p7	22:35323199	GCCAGGACAGGGCAG[A/G]GCACGGCCAGGAAGA	10043
rs779492546	snp	A/G	1.64781e-05	0.00287033	missense, nc-transcript-variant, intron-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35322015	GGAATAAGAACTTCC[A/G]CGAGGTGATGCTGGC	10043
rs779559343	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35341008	GTGGTGTGTGACCTG[C/T]CACCAAGCACAGCAC	10043
rs779586928	snp	A/C	1.6638e-05	0.00288422	intron-variant	TOM1	GRCh38.p7	22:35322080	GCAGGACTACGGTCC[A/C]CTGAAAGTCACCTCC	10043
rs779620228	in-del	-/TG	0.000199064	0.0099746	intron-variant	TOM1	GRCh38.p7	22:35323473	GCTGTGGTTACCGGC[-/TG]TGTCCCCTTGTCCCC	10043
rs779629370	in-del	-/AGCTGCAGAC	1.68977e-05	0.00290665	intron-variant	TOM1	GRCh38.p7	22:35333359	GGCAGAAAGGAACGA[-/AGCTGCAGAC]AGCGGGGATGATCAG	10043
rs779643136	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35300478	ACTGGCCAGAGGGGC[C/T]CAGCGCCGGACAGCC	10043
rs779689376	snp	C/T	1.81115e-05	0.00300922	intron-variant	TOM1	GRCh38.p7	22:35323925	AACAGGTAAACGAGC[C/T]TGGGGTCAGAACCGT	10043
rs779779538	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35305182	AGACACCAGGCTGGG[A/G]GGCGGGACACCTGGT	10043
rs779893591	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35310509	CAGTGAGCCGAGATC[A/G]TGCCACTGCACTCCA	10043
rs779932190	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35326372	CCACAGCATAAGATC[C/T]TTATACCAATGGCCT	10043
rs779949839	snp	A/T	1.64779e-05	0.00287031	missense, intron-variant, nc-transcript-variant	TOM1	GRCh38.p7	22:35323587	GCCTGGAGTTCCCCA[A/T]GACTGACCTGGACAT	10043
rs779959720	snp	A/G	8.42652e-05	0.00649041	intron-variant	TOM1	GRCh38.p7	22:35333372	GAAGCTGCAGACAGC[A/G]GGGATGATCAGGGCA	10043
rs780055027	snp	C/G	1.72594e-05	0.00293758	intron-variant	TOM1	GRCh38.p7	22:35330304	AGAGACGGCCTCACT[C/G]TGAGTCATGTGACTG	10043
rs780102365	in-del	-/G			intron-variant	TOM1	GRCh38.p7	22:35303972	AGCAGGAAGGAGGAA[-/G]GGAGAAAAGGAAAGT	10043
rs780135917	snp	C/T	1.64988e-05	0.00287213	missense, nc-transcript-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334441	TCACTGGCTGACCAA[C/T]GGAAAGAGTGAGTGG	10043
rs780156731	snp	A/G	0.000296467	0.0121715	missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35332989	CTTGTAGGTTTGAAC[A/G]GTTCCGAACAGGCCA	10043
rs780241918	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35314849	CTGTGTGCCCTTTGC[A/G]AGTTGGTGATCTCTC	10043
rs780298986	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35303955	CACGGTGCCTGGCAC[A/G]TAGCAGGAAGGAGGA	10043
rs780319038	snp	G/T	0.000148262	0.00860865	utr-variant-5-prime, missense, nc-transcript-variant	TOM1	GRCh38.p7	22:35317915	CAGAGCGAGGACTGG[G/T]CCCTCAACATGGAGA	10043
rs780345630	snp	A/G	5.2017e-05	0.00509959	synonymous-codon, nc-transcript-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35338734	ATACGAAGCCCCCCA[A/G]GCAACAGACGGCCTG	10043
rs780429369	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35319107	GTGAGGGTGAGGGAA[A/G]GAGTGGTGGGCAGAG	10043
rs780447355	snp	A/G			intron-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35337847	GAAGTCCTGTCTGCC[A/G]GCAGTTCAGGGCGAG	10043
rs780464794	snp	C/T	3.33611e-05	0.00408405	intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334277	AGCTCAGCAGCAGCT[C/T]ACACACAAGCTTGTG	10043
rs780470993	snp	C/G	0.000105734	0.00727021	utr-variant-3-prime, nc-transcript-variant	TOM1	GRCh38.p7	22:35347235	TGGCACCCTGCAGCC[C/G]AGGTCCCCACTGCTC	10043
rs780518383	snp	C/T	8.28013e-05	0.0064338	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35323093	GGCCAGCCAGGACTT[C/T]GTGGAGAGTGTGCTG	10043
rs780573900	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35302626	CATGACCACCGTGTC[C/T]GGCCTAGAATGTGAA	10043
rs780621838	snp	C/G			intron-variant	TOM1	GRCh38.p7	22:35344016	TCATACACCTACACA[C/G]ACACCTACACTCATA	10043
rs780633927	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35325305	ATTTGAACTCATTCT[C/T]ACCCTAACCTATTTG	10043
rs780651664	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35318447	GTGAAGCTGAACCGT[A/G]AGCCTGAACAGCACT	10043
rs780705191	snp	A/C			intron-variant	TOM1	GRCh38.p7	22:35300768	CGCAGCCTCCCTGGG[A/C]CGAGGTTTCCTCACC	10043
rs780714554	snp	C/T	3.37183e-05	0.00410585	intron-variant, nc-transcript-variant	TOM1	GRCh38.p7	22:35323012	AGGTGCTCGACGGCA[C/T]CTCTCGGCCCTCCAG	10043
rs780725033	snp	A/G	1.70177e-05	0.00291694	intron-variant	TOM1	GRCh38.p7	22:35323746	CCAGGAGCCCTCACT[A/G]ATCCTGTTTTCCTCC	10043
rs780757860	snp	G/T			intron-variant	TOM1	GRCh38.p7	22:35318330	GGCGGGAGTGTGTAC[G/T]AGAGAGACTCCGGCT	10043
rs780778465	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35345185	TGTCTGGTTAACTTC[A/G]CGCCTCTGCTCTCAG	10043
rs780780463	snp	A/G			intron-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35335395	TAGGTCCTTAGGGCT[A/G]CCCTGGCTGTTAGCT	10043
rs780807621	snp	A/G	2.67964e-05	0.00366025	intron-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35321839	AACCTGGCTGGATAC[A/G]CAAAACAGGTGGGGC	10043
rs780817226	snp	C/T	0.000386473	0.0138956	intron-variant	TOM1	GRCh38.p7	22:35331284	TTTCTTTTTTTTTTT[C/T]TCTTTTTGCAGAGAC	10043
rs780838595	snp	A/G	1.64806e-05	0.00287054	missense, nc-transcript-variant, upstream-variant-2KB	TOM1, MIR3909	GRCh38.p7	22:35334382	TGGAGGCCTCTGGTC[A/G]ACTGGAAGATGAGTT	10043
rs780935006	in-del	-/GCTCCGCCCCGGT	0.000251225	0.0112049	intron-variant	TOM1	GRCh38.p7	22:35300004	CTGGAGCCCCCCACA[-/GCTCCGCCCCGGT]GCTCCGCACCCAGCT	10043
rs780990957	snp	A/G	9.885e-05	0.0070296	missense, nc-transcript-variant, intron-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35321996	GTAAAGAAGAGAATC[A/G]TGGGGAATAAGAACT	10043
rs781020541	snp	A/T	1.6861e-05	0.00290348	intron-variant	TOM1	GRCh38.p7	22:35323211	CAGGGCACGGCCAGG[A/T]AGAGCTGTCAGTGCA	10043
rs781095070	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35315807	CCGCAGAAACTGCCC[C/T]CCTCTGTCCTCCGGC	10043
rs781187000	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35316313	CAGCCAGAGTGATGT[A/G]TGTAATGGAACGTTA	10043
rs781264342	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35305257	TTGCCCATCTCCCCT[A/G]TTGGCAACACAGAGG	10043
rs781264866	snp	C/T	1.66774e-05	0.00288763	synonymous-codon, nc-transcript-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35323030	CTCGGCCCTCCAGGT[C/T]TTAGAAACCTGTGTC	10043
rs781266807	snp	A/C			intron-variant	TOM1	GRCh38.p7	22:35311353	GTCTGAAACCACCAC[A/C]ACAACGCACTTTGTT	10043
rs781323401	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35312439	GATTTGCTCACTGAC[A/G]TCTCCCTGTAGCCTG	10043
rs781400342	snp	C/T	1.65332e-05	0.00287512	missense, intron-variant, nc-transcript-variant, utr-variant-5-prime	TOM1	GRCh38.p7	22:35323496	CTTGTCCCCTCTCAG[C/T]CCTGGGCTGACGCGT	10043
rs781457631	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35306106	AAATTTGAATTTCAC[A/G]TAATTTTCACATATC	10043
rs781462062	snp	A/C/T	8.49054e-05	0.00651509	intron-variant, nc-transcript-variant	TOM1	GRCh38.p7	22:35323007	GACCAAGGTGCTCGA[A/C/T]GGCACCTCTCGGCCC	10043
rs781489033	snp	A/G	0.000131036	0.00809325	missense, nc-transcript-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35338723	TTCAGGGTAAAATAC[A/G]AAGCCCCCCAAGCAA	10043
rs781517150	in-del	-/T			intron-variant	TOM1	GRCh38.p7	22:35343734	ACACATCTACACCCA[-/T]CCACACCTACACACA	10043
rs781621652	snp	A/G			upstream-variant-2KB	TOM1	GRCh38.p7	22:35297643	CAGCTAATTTTTTCT[A/G]TTTTTTTAGTAGAGA	10043
rs781639521	snp	A/T			intron-variant, upstream-variant-2KB	TOM1, MIR6069	GRCh38.p7	22:35337980	TTAGCCAGCTTCTCC[A/T]CTCACTCAGGTTATT	10043
rs781656945	snp	C/T	2.00648e-05	0.00316733	intron-variant	TOM1	GRCh38.p7	22:35327431	TCAGATGACTCCTGC[C/T]CAGCTGCCCACATGC	10043
rs781721807	snp	G/T			intron-variant	TOM1	GRCh38.p7	22:35326717	AGTCCTCTAGGAGGA[G/T]AGAGGGCGGGATCCC	10043
rs781749410	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35315171	AGGCGGTAGTCTAGC[A/G]GGAGGATGGTGGCCG	10043
rs781757634	snp	A/G			intron-variant, downstream-variant-500B	TOM1, MIR3909	GRCh38.p7	22:35335933	AGAGGCAGGGCGGGA[A/G]AGAGGTGCCCTGGCT	10043
rs796065360	in-del	-/TC			intron-variant	TOM1	GRCh38.p7	22:35308235	GTGTGTGTGTGTCTG[-/TC]TCTCTCTCTCTCTCT	10043
rs796146259	snp	A/T			intron-variant	TOM1	GRCh38.p7	22:35306283	GAGGCAGAATGATGG[A/T]GCACACTGTTCCTCA	10043
rs796165362	in-del	-/T			intron-variant, downstream-variant-500B	TOM1, MIR3909, MIR6069	GRCh38.p7	22:35336256	CTGAGCATCCATTTC[-/T]GTCTTCCCTTTGTTC	10043
rs796295620	snp	A/T			intron-variant	TOM1	GRCh38.p7	22:35322512	TCCTAGCCGTCAGCA[A/T]GGGTTTGGCTGGGGA	10043
rs796354958	in-del	-/ACA			intron-variant	TOM1	GRCh38.p7	22:35343934	CACACACATCTACAC[-/ACA]CCACCTACACACACC	10043
rs796597049	in-del	-/CAC			intron-variant	TOM1	GRCh38.p7	22:35343179	CACCACACCTACACA[-/CAC]CACACCTCCACTCAT	10043
rs796603500	in-del	-/A			intron-variant	TOM1	GRCh38.p7	22:35312259	AAAAAAAAAAAAAAA[-/A]GACAAGGGGAGTTCA	10043
rs796609905	in-del	-/AC			intron-variant	TOM1	GRCh38.p7	22:35300905	GCCATATAAAAAAAA[-/AC]AGTTGTAATATTTAT	10043
rs796640901	in-del	-/A			intron-variant	TOM1	GRCh38.p7	22:35320988	CTCTGTCTCAGAAGG[-/A]AAAAAAAAAAAAACT	10043
rs796804227	snp	A/G			intron-variant	TOM1	GRCh38.p7	22:35316375	GTGCACGTGGTTGAC[A/G]CGTGAAGATAGCATC	10043
rs796879172	snp	C/T			intron-variant	TOM1	GRCh38.p7	22:35330580	ATCTGAGCCTTCTCT[C/T]GTCCTCCTCTCAAAC	10043

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