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

TMF1

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs551591550	snp	A/T	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69038143	AAGTATAAATAACCC[A/T]TATGCCCATCAACTG	7110
rs551782084	snp	C/T	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69051353	GGTGGTGGGCGCCTG[C/T]AATCCCAGCTACTAG	7110
rs551974466	snp	C/T	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69023383	TCTTTAATATTTATA[C/T]TGCCATAGGAGTCAA	7110
rs552018794	snp	G/T			intron-variant	TMF1	GRCh38.p7	3:69033348	ATCTGATACCATTGT[G/T]TAATGGGAAAAAATG	7110
rs552122583	snp	C/T	0.000798403	0.0199641	intron-variant	TMF1	GRCh38.p7	3:69040488	TTTCAAATGAGTTGA[C/T]AAAAGGGTAGTGTAT	7110
rs552181575	snp	A/G	0.00159617	0.0282053	intron-variant	TMF1	GRCh38.p7	3:69032858	TCAAGTGATCCACCC[A/G]CCTAGGCCTCCCAAA	7110
rs552268386	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	TMF1	GRCh38.p7	3:69052509	GATAGAGGTCGATTT[C/T]CCCGGAAGGAATATT	7110
rs552322263	snp	A/G	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69034201	TCTTTGGCCAGGCAC[A/G]GTGGCTCATGTGTGT	7110
rs552335311	snp	C/T	0.00119737	0.0244387	intron-variant	TMF1	GRCh38.p7	3:69046057	AGAGACCCTGTGAGC[C/T]GCGATCGCACCACTG	7110
rs552340998	in-del	-/C			intron-variant	TMF1	GRCh38.p7	3:69046235	TCTAATTCCTTAGGT[-/C]CTACTCAAATGGTGA	7110
rs552371315	snp	C/T	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69027156	ACATGCCACCATGCC[C/T]GGCTAATTTTTGTAT	7110
rs552379448	snp	A/T	0.00159617	0.0282053	intron-variant	TMF1	GRCh38.p7	3:69032091	TTTTTCTAGACCAAA[A/T]CTTTCATGGAACTCC	7110
rs552398573	snp	A/G	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69046555	TACATGGCACTTACA[A/G]GACATTTCTTCAAGA	7110
rs552469538	snp	A/G			utr-variant-3-prime	TMF1	GRCh38.p7	3:69020332	CACTGTACAACTGGC[A/G]ATTCTCAAAAAATAG	7110
rs552478304	snp	C/G	0.000798403	0.0199641	upstream-variant-2KB	TMF1	GRCh38.p7	3:69053015	AGCCAGAATAGCAGC[C/G]CTCACCAGACACCAA	7110
rs552667261	snp	A/G	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69051421	CGGAGGTTGCAGTGA[A/G]CCGAGATCGCGCCAC	7110
rs552777040	snp	C/T	0.000798403	0.0199641	intron-variant	TMF1	GRCh38.p7	3:69030444	ACAAGGCAGATTTGA[C/T]ACAAAAAGCAAGAGC	7110
rs552795510	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	TMF1	GRCh38.p7	3:69022703	TACTTTAACACTTAA[C/T]GTACATTTTCATGAG	7110
rs552809093	snp	C/T	0.000798403	0.0199641	intron-variant	TMF1	GRCh38.p7	3:69044291	AGTTTTCCAGTTTTG[C/T]AAAATGACTCTCTTC	7110
rs552853657	snp	A/C	0.000798403	0.0199641	intron-variant	TMF1	GRCh38.p7	3:69035759	TACAATAAATGTATA[A/C]AACATGTAAAAAAAA	7110
rs553040315	in-del	-/C	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	TMF1, MIR3136	GRCh38.p7	3:69050271	CTCAAAAAAAAAAAA[-/C]AACAAAAAAACAAAT	7110
rs553370849	snp	C/T	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69032408	ATTTTATCACTACAC[C/T]GTGATTTCTCAAATT	7110
rs553379087	snp	A/G	0.00119737	0.0244387	intron-variant	TMF1	GRCh38.p7	3:69043408	CTCCTGGGCTCAAGC[A/G]ATCCACCCTCTTCGG	7110
rs553448896	snp	G/T	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69025470	ATCTTGTTTCTCAAT[G/T]TGCTCAGAATTCAGA	7110
rs553574462	snp	C/T	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69038264	GAGTTAAATGGATTC[C/T]CTCAAAATTATATGC	7110
rs553707302	snp	A/C	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69031665	AGAGCAATGGGTAAG[A/C]TTCTGAGATTTAACC	7110
rs553708834	snp	A/G	0.00159617	0.0282053	intron-variant	TMF1	GRCh38.p7	3:69039398	TGAGCCACCCCACTC[A/G]GCTAAAAAATCTTAT	7110
rs553774057	snp	A/G	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69033333	AGTACTTTAGCCAGT[A/G]TCTGATACCATTGTG	7110
rs553782809	snp	A/G	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69046927	TAATATTTGCTACAA[A/G]TAATGTAAACATGTA	7110
rs553808487	snp	A/G	1.65655e-05	0.00287793	missense	TMF1	GRCh38.p7	3:69047596	CCTTCAGCAGATTCA[A/G]CTGTTTTAGACTTTG	7110
rs553858679	in-del	-/A			intron-variant	TMF1	GRCh38.p7	3:69024929	AGCATGTCAGCACTC[-/A]AAGTTTTGGATTTGG	7110
rs554005748	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, utr-variant-5-prime	TMF1	GRCh38.p7	3:69052334	AGCAACCAAATCTAC[C/G]AGCCCAGAGTTCGGT	7110
rs554056519	snp	C/T	0.00119737	0.0244387	intron-variant	TMF1	GRCh38.p7	3:69027105	GGTTCAAGCAATTCT[C/T]CCACCTCTGCCTCCC	7110
rs554068376	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	TMF1	GRCh38.p7	3:69052720	AAAAGACAGGATCAC[A/G]TATGAACACTGTGTC	7110
rs554184121	snp	C/T	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69039076	TAAATAACTGTATTC[C/T]AGGAATCTATAATAA	7110
rs554245185	snp	C/G	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69039372	CTCCGAAAGTGTTGG[C/G]ATTACAGGCGTGAGC	7110
rs554260190	snp	C/T	0.000798403	0.0199641	intron-variant	TMF1	GRCh38.p7	3:69040813	TATAGTCTCAGCTAT[C/T]CGGGAGGCTGAGGCA	7110
rs554308410	snp	A/G	0.000798403	0.0199641	intron-variant	TMF1	GRCh38.p7	3:69046200	AGTATAAAGCTAAAC[A/G]AAAAGTAATGCTTGG	7110
rs554394906	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69024605	TTAGGTCCCTGTATA[A/G]CATACCAGCTATACA	7110
rs554525832	snp	A/G	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69045502	ATAAAAGTAGAGGCC[A/G]GGCATGGTGGCTCAT	7110
rs554600797	snp	G/T	0.00279162	0.0372561	upstream-variant-2KB	TMF1	GRCh38.p7	3:69053731	TTTCAAACAGCTAAG[G/T]AGTCTGCAGAGGAGA	7110
rs554707288	snp	A/C	0.00119737	0.0244387	intron-variant	TMF1	GRCh38.p7	3:69033224	GCTTGCAGTGAGCCG[A/C]GATCGCGCCACTGCA	7110
rs554766844	snp	A/C	1.65644e-05	0.00287783	missense	TMF1	GRCh38.p7	3:69033611	GGGATCCCAGGGTTG[A/C]TTGCAAATTTTCTAT	7110
rs554863042	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime	TMF1	GRCh38.p7	3:69052281	AGCTGAGACGAAGGG[A/G]GCCCATGTGCGCATG	7110
rs554951619	snp	A/G	0.00199481	0.0315187	intron-variant	TMF1	GRCh38.p7	3:69026956	TAACTCCAAGTACAC[A/G]GTAATTCTTTCAATA	7110
rs555064282	snp	A/G	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69047091	TTTTGAAGTGATAAG[A/G]ACTCAAAAATAAAGA	7110
rs555154145	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	TMF1	GRCh38.p7	3:69020854	TTTAATTTTATAAAA[C/T]TGAAAAGTTTAGGAA	7110
rs555193345	snp	C/T	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69026425	AACATGGAAAAACCT[C/T]GTCTCTACTAAAAAT	7110
rs555253232	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69031258	GGGAGGAAGGGTTGA[A/G]AGAGTGGTAGGTGTG	7110
rs555275161	snp	A/C			intron-variant	TMF1	GRCh38.p7	3:69046629	AAATTTGTATATCTA[A/C]AAGTCACAGTAAAAA	7110
rs555276262	in-del	-/CA			intron-variant	TMF1	GRCh38.p7	3:69032322	ATAAGTGACTTGTTC[-/CA]CACTGTTTTGCTGGA	7110
rs555312854	snp	A/G	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69040741	AGCCTGGCCAACATG[A/G]TGAAACCCCATCTCT	7110
rs555456139	snp	G/T	0.000164596	0.00907032	intron-variant	TMF1	GRCh38.p7	3:69042567	CAGCACAAATTTCTG[G/T]CTATTTTACAGGGAC	7110
rs555516012	in-del	-/T	0.00318978	0.0398085	intron-variant	TMF1	GRCh38.p7	3:69030313	AAAAACCAAAAAGCC[-/T]TACACATCACATCAT	7110
rs555706833	snp	A/C			intron-variant	TMF1	GRCh38.p7	3:69024751	TTGTGTTTAACACTG[A/C]AAAGAGGTATCCTGA	7110
rs555902928	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime	TMF1	GRCh38.p7	3:69021333	CCATGGGTAAGAGGG[A/T]ACTACTATATTTTCT	7110
rs556000543	snp	A/C/G	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69027458	ATATTTCAAGTCCTA[A/C/G]AAATCATAGATCTCT	7110
rs556084277	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	TMF1	GRCh38.p7	3:69053569	GAACTCTGCAAAAAA[A/G]AATTATTTTTCTTTT	7110
rs556110039	snp	C/G	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69033897	GTGCAGTGGCACAAT[C/G]GTGGCTCACTGTAGC	7110
rs556112641	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TMF1, MIR3136	GRCh38.p7	3:69049317	AGGTGGAAGCTGCAG[G/T]GAGCCATGATCAAAC	7110
rs556199438	snp	A/T	0.000798403	0.0199641	intron-variant	TMF1	GRCh38.p7	3:69041765	ACTAGAAAAAATTAA[A/T]AGTTCCTTATAATAT	7110
rs556280719	snp	C/G	3.71188e-05	0.0043079	intron-variant, downstream-variant-500B	TMF1, MIR3136	GRCh38.p7	3:69048569	AACTTATTCCTTTAA[C/G]AAAAAAGTAAATATT	7110
rs556291363	snp	G/T	0.000399281	0.0141238	downstream-variant-500B	TMF1	GRCh38.p7	3:69019780	ATATTCATTCTTCAC[G/T]CATTACTATTGACCA	7110
rs556325562	in-del	-/A	0.00026908	0.011596	intron-variant	TMF1	GRCh38.p7	3:69030022	CTGATTACAGGACAG[-/A]AAAAAAAAATCACAT	7110
rs556445577	snp	C/T	4.98351e-05	0.0049915	synonymous-codon	TMF1	GRCh38.p7	3:69047424	TTCACACTGCTCAGC[C/T]ACCTTGTCTAACACA	7110
rs556539135	snp	G/T			utr-variant-3-prime	TMF1	GRCh38.p7	3:69021683	AAATTAAATAAGAGT[G/T]TGTTTTTTTTTTTTT	7110
rs556580880	snp	C/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	TMF1, MIR3136	GRCh38.p7	3:69049237	TAATTAGCTGGGCCT[C/G]GTGGCCCACATATGT	7110
rs556716990	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69037114	AAATGTGCAAAGGAT[C/T]TGAATATTTTAATTA	7110
rs556730464	snp	A/C			intron-variant	TMF1	GRCh38.p7	3:69045151	TTTTTAAAATATGAC[A/C]TATTGCATTTAAAAA	7110
rs556784630	snp	A/G	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69037076	CTCATAATAACAATA[A/G]AAAGACAAACCGCCC	7110
rs556794172	snp	C/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	TMF1, MIR3136	GRCh38.p7	3:69050216	AGTGAACAGAGATGG[C/G]ACCACTGCACTCCAG	7110
rs556925113	snp	C/T	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69029441	TTGTTTATTTACTTA[C/T]TTAATTTATTTTTTT	7110
rs557095897	in-del	-/AAGT	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	TMF1, MIR3136	GRCh38.p7	3:69049912	TGGTGGAGAGAGCAC[-/AAGT]AACTAAAAGCTTCTA	7110
rs557231888	snp	C/T	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69029736	GTGAGCCACGGCGCC[C/T]GGCCCAACAACATAC	7110
rs557392645	snp	A/G	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69044685	TGTAACAAAGAAAAC[A/G]GCTTTATCTCATAAA	7110
rs557440291	snp	A/C	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69024683	TTCTTTAATATTTTC[A/C]TATAACTAAAAGTAT	7110
rs557509397	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TMF1, MIR3136	GRCh38.p7	3:69050927	TAGACTTAAGAGTCA[A/G]AAGCAACTGAATGAA	7110
rs557512548	snp	A/G	0.00199481	0.0315187	intron-variant	TMF1	GRCh38.p7	3:69041646	ACAGCCACTAATAAT[A/G]ATAAAAAGCATTTAA	7110
rs557548870	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69033051	ACTACTGCAGACAAG[C/T]TACAAAGGGGTCAGA	7110
rs557585923	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69035395	ATATTGGAGAAAAGA[C/T]AGTGCGTCTATAAAT	7110
rs557687596	snp	A/G	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69037630	CTGGGCAACAAGAGC[A/G]AAACTCTGTCTCACA	7110
rs557850616	snp	A/C	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69037180	CAAATGAAAAGACAT[A/C]CAACATCATTAGTCA	7110
rs558039220	snp	G/T	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69036196	ATCATCAGGATATTT[G/T]ACTAAGTAAATAAAA	7110
rs558102752	snp	G/T	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69028657	AAAAGTTCAGATATT[G/T]TACTTTAGAAATCAT	7110
rs558191464	snp	A/G	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69044937	ATAAATGCACTAGGC[A/G]ACATGTATAAGAATA	7110
rs558249219	snp	A/C			intron-variant	TMF1	GRCh38.p7	3:69031730	GTAGAGCTAGTAATA[A/C]CTCTATTTCACATTT	7110
rs558285530	snp	A/G	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69023894	TGAATATGTAAAGAT[A/G]CAAGCAAGATAAAAG	7110
rs558324934	snp	C/G	0.00159617	0.0282053	utr-variant-5-prime	TMF1	GRCh38.p7	3:69052237	AGCCTCCCGCGAGCC[C/G]GGGATGTTACCCTCG	7110
rs558373926	snp	C/T	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69024479	AAATGACATATATTT[C/T]AGTTATTCTAAATTA	7110
rs558436831	snp	G/T	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69031490	TAAAATCAGTAGATT[G/T]TATCAATGTCAATAC	7110
rs558449961	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TMF1, MIR3136	GRCh38.p7	3:69050167	CGGGAGGTTGAGGCA[C/T]GAGAATCACTTGAGC	7110
rs558506655	snp	A/G	0.000798403	0.0199641	intron-variant	TMF1	GRCh38.p7	3:69043587	GCTGGGATTATAGAC[A/G]TGAGCCACCACACGT	7110
rs558506828	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TMF1, MIR3136	GRCh38.p7	3:69050835	CAAGTACATCTCTTA[C/T]CCTTTTTCACACAAA	7110
rs558524306	snp	A/C	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69051477	GAGACTCCGTCTCAA[A/C]AACAACATAAAACCA	7110
rs558633787	snp	A/C	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69026292	CCCATAAAATGGCTT[A/C]TTAAGTCAAAAATAC	7110
rs558653821	snp	G/T			utr-variant-5-prime	TMF1	GRCh38.p7	3:69052185	GCTCCCCTTTTCCAC[G/T]CGGCTGGTTCTGTCA	7110
rs558924700	snp	C/G/T	0.00438332	0.0466095	intron-variant	TMF1	GRCh38.p7	3:69043555	CAAGTGATCCGCCCA[C/G/T]TTCAGCCTCCCAGTG	7110
rs558936624	snp	C/T	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69047156	AAGTATCAACTTATT[C/T]TACCATAATTGCCTT	7110
rs558995481	snp	A/G	0.000798403	0.0199641	intron-variant	TMF1	GRCh38.p7	3:69033147	GGCATGGTGGCAGAC[A/G]CCTGTAATCCCAGCT	7110
rs559012356	snp	C/T	0.000798403	0.0199641	intron-variant	TMF1	GRCh38.p7	3:69040548	GGCAAGATGTTAACA[C/T]CTGATGAATCTAGGT	7110
rs559045567	snp	A/C	0.00119737	0.0244387	upstream-variant-2KB	TMF1	GRCh38.p7	3:69052883	TAATCTCCAATGGGA[A/C]AGTATTAAGGGGAGC	7110
rs559219231	snp	C/T	1.65712e-05	0.00287843	missense	TMF1	GRCh38.p7	3:69025635	GCTTGATCCTGCTCC[C/T]ATCCTTACAGCATCA	7110
rs559257144	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TMF1, MIR3136	GRCh38.p7	3:69049616	TTCAGAAATGTGTGT[G/T]TTTTTAAGAACTATT	7110
rs559673100	snp	C/G	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69037693	TGCCTGTAGTCCCAG[C/G]TACTCAGGAGGCTGA	7110
rs559825650	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69037989	AGCCACTGTGGAAAA[A/G]TTTGCCAGTTCCTCA	7110
rs559834999	snp	C/G	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69026489	TAATCCCAGCTACTC[C/G]GGAGGCTGAGGCAGA	7110
rs559855913	snp	C/T	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69051331	AATACAAAAAGTTGC[C/T]GGGCGTGGTGGTGGG	7110
rs559874579	snp	A/G	0.000798403	0.0199641	intron-variant	TMF1	GRCh38.p7	3:69032743	GCCTCCCAAATAGCT[A/G]GGATTACAGGCATGC	7110
rs559919884	snp	A/G	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69051667	GAGGGAGAGCTTGAG[A/G]GCAAGACCAACCAAC	7110
rs560035932	snp	C/T	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69031992	GCTGTCAGAGATAAA[C/T]GACAGACCTAACATT	7110
rs560108984	snp	A/G	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69047143	CTTAACTGTATTGAA[A/G]TATCAACTTATTCTA	7110
rs560109600	snp	C/G	1.66391e-05	0.00288431	missense	TMF1	GRCh38.p7	3:69024180	GATTGCCAATTTCTA[C/G]CTGAGAAGCATTACC	7110
rs560115582	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69033853	TATTAATTTTAGAAA[C/T]GGGGTCCCGCTCTGT	7110
rs560209554	snp	C/T			utr-variant-3-prime	TMF1	GRCh38.p7	3:69022462	CATTATCCAATCACA[C/T]CTAGATAACATTGAA	7110
rs560403398	snp	C/G	0.000798403	0.0199641	intron-variant	TMF1	GRCh38.p7	3:69034106	GCATGAACCACCATG[C/G]CCAGCCCTTAATTAT	7110
rs560462851	snp	C/T			upstream-variant-2KB	TMF1	GRCh38.p7	3:69053469	GCCACAGACCCCTAT[C/T]ACTCATCCTATTACA	7110
rs560473112	snp	C/G			downstream-variant-500B	TMF1	GRCh38.p7	3:69019781	TATTCATTCTTCACT[C/G]ATTACTATTGACCAC	7110
rs560652600	snp	A/G	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69032674	GGAGTGCTGTAGCGC[A/G]ATCTCAGCTCACTGC	7110
rs560762408	in-del	-/A	0.0023933	0.0345097	utr-variant-3-prime	TMF1	GRCh38.p7	3:69020285	ATCTTAAGTCACAAC[-/A]TAGATATATTTGGTA	7110
rs560779940	snp	G/T			intron-variant	TMF1	GRCh38.p7	3:69029055	TTATTTTTTTTTTTT[G/T]GGAGACGGAGTCTCG	7110
rs560863788	snp	C/T	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69037833	ATTGAAAAAAAAAAA[C/T]GCAAATCAACACCAT	7110
rs560876896	snp	A/G/T			utr-variant-5-prime	TMF1	GRCh38.p7	3:69052313	GCTTGCTTCTTCCAC[A/G/T]TACACAGCAACCAAA	7110
rs560939632	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	TMF1	GRCh38.p7	3:69052930	GATGATGATGGAGCC[C/G]TCATAAATGGGGTTA	7110
rs560976528	snp	A/C	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69051512	ACGCGCTACCAAGCG[A/C]GAAATGTTCACTGAC	7110
rs561061677	snp	C/T	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69025068	CATCAACAACTCATG[C/T]TGTTTCCTCCCATGT	7110
rs561158492	snp	G/T			intron-variant	TMF1	GRCh38.p7	3:69045918	CAAAAAAATAGCCAG[G/T]CGTGGTGCGAGCCTA	7110
rs561286054	snp	A/G	3.38765e-05	0.00411547	intron-variant	TMF1	GRCh38.p7	3:69025747	TCACACAGTTACTCA[A/G]TTATCATAGCTTGTC	7110
rs561297966	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69037200	ATCATTAGTCATTAA[A/G]AGAATGCAAATCAGC	7110
rs561328693	snp	C/T	0.000798403	0.0199641	intron-variant	TMF1	GRCh38.p7	3:69045919	AAAAAAATAGCCAGG[C/T]GTGGTGCGAGCCTAT	7110
rs561726684	snp	A/T	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69035681	TGGAAATATTCTAAA[A/T]CTCCATCACTAGTAA	7110
rs561731763	snp	A/G	0.000399281	0.0141238	downstream-variant-500B, upstream-variant-2KB	UBA3, TMF1	GRCh38.p7	3:69054235	AGAAACAAAAACATG[A/G]TCAGGCATGGTGGCT	7110
rs561748335	snp	G/T			synonymous-codon	TMF1	GRCh38.p7	3:69026086	GCTAGAAACAGAAAA[G/T]GGCTTGCGTTCCTTA	7110
rs561769538	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime	TMF1	GRCh38.p7	3:69019851	TAAAATCTTTATTCA[A/G]TCAGATCCATGCTTA	7110
rs561794015	in-del	-/A			intron-variant, upstream-variant-2KB	TMF1, MIR3136	GRCh38.p7	3:69050259	GTGAGACTGTGTCTC[-/A]AAAAAAAAAAAAAAC	7110
rs561897272	snp	C/G	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69040365	TTCTGAATTAATGCT[C/G]ATTTCTTAGGTTTGA	7110
rs561898033	snp	A/C	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69026638	AAACAAACAAACAAA[A/C]AAAAAGTACAATATT	7110
rs561904220	snp	G/T	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69033997	TTTTGTATTTTTTTG[G/T]AGAGACGAGGTTTCA	7110
rs561983955	snp	A/G			upstream-variant-2KB	TMF1	GRCh38.p7	3:69053474	AGACCCCTATCACTC[A/G]TCCTATTACACCCTC	7110
rs562061695	snp	C/G	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69035196	TACATATTTTGTGTT[C/G]TGTCAACATTGTTCA	7110
rs562200198	snp	A/T	0.000798403	0.0199641	intron-variant	TMF1	GRCh38.p7	3:69040991	TTGTGAAATGTAAAT[A/T]CTCTGTGAATATAAA	7110
rs562423879	snp	A/T	0.000798403	0.0199641	intron-variant	TMF1	GRCh38.p7	3:69041915	AGAGAGATTCACTTG[A/T]CCACGTTTTCCAAAG	7110
rs562580878	snp	A/T	1.65611e-05	0.00287755	missense	TMF1	GRCh38.p7	3:69035057	TCATGGCGTAAATAA[A/T]CCTCCTTTCTGGCAG	7110
rs562634049	in-del	-/T			utr-variant-3-prime	TMF1	GRCh38.p7	3:69022888	CTTCTTCTCTAGCCA[-/T]ATTTATATGAGGATA	7110
rs562664537	snp	C/T	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69033434	TAAAAATCTACATAT[C/T]AGACACAAAATGTAA	7110
rs562671321	snp	C/T	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69039230	AGCTGGGACTACAGA[C/T]GTGCACCACCACGCC	7110
rs562671846	snp	C/T			upstream-variant-2KB	TMF1	GRCh38.p7	3:69054032	TTATTTGTCAATATG[C/T]AGCTAGAAAGATTAC	7110
rs562734612	snp	A/C	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69039454	TTCTTACATGATATA[A/C]CCCATTAAATCTTTT	7110
rs562841108	snp	G/T	2.47638e-05	0.00351871	missense	TMF1	GRCh38.p7	3:69027901	ACAAAATTCAATACC[G/T]TTTCTTTTATTGTTT	7110
rs562856189	snp	G/T	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69040494	ATGAGTTGACAAAAG[G/T]GTAGTGTATGTATGT	7110
rs562929952	snp	A/T	0.00119737	0.0244387	upstream-variant-2KB	TMF1	GRCh38.p7	3:69053994	AGCTTATAAATTTAT[A/T]CCGTATGGTTTTATA	7110
rs562991853	snp	A/G	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69047287	TATGCATCAATGAAA[A/G]TATTTTTTAAAACAA	7110
rs563119465	snp	A/C			intron-variant	TMF1	GRCh38.p7	3:69032955	TGTCTCTTCTAAGGT[A/C]GATCTTGACTCTCCT	7110
rs563124650	in-del	-/T	0.00159617	0.0282053	utr-variant-3-prime	TMF1	GRCh38.p7	3:69020904	TCTCTGCAAATGAAG[-/T]TTTTTTTCTACTAGT	7110
rs563126934	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	TMF1, MIR3136	GRCh38.p7	3:69048829	CTGGACTACCAGATG[C/T]GAGTATGTTATTCCT	7110
rs563347156	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TMF1, MIR3136	GRCh38.p7	3:69049487	AGAACAAATTCATTT[C/T]CATCCACTTAATCAC	7110
rs563388499	snp	G/T	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69043011	CTGTCCATAATCACA[G/T]TTGCAATAAGAATCT	7110
rs563486330	snp	C/T	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69028739	TTAAAAAATACTAAC[C/T]ATTGCCTTAATATAA	7110
rs563662909	snp	C/T	1.81787e-05	0.0030148	utr-variant-3-prime	TMF1	GRCh38.p7	3:69023131	CATTAAATGTTTAGA[C/T]ATTAAATGCTTACAT	7110
rs563736083	in-del	-/T	0.030665	0.119967	intron-variant	TMF1	GRCh38.p7	3:69038318	TCTCTTCTAAGAGGG[-/T]TTCCTAGCTTTTATA	7110
rs563768041	snp	C/T	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69029637	GGAGAGAGTAGGTTT[C/T]GCCATGTTGGCCAGG	7110
rs563841067	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69039429	CATTTATCTATTGTT[C/T]GAAAAATCCTTCTTA	7110
rs564025548	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime	TMF1	GRCh38.p7	3:69020943	TAAAGGGACTATTTT[A/G]TAATTCCAAAACGTC	7110
rs564167979	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	TMF1	GRCh38.p7	3:69021922	CTCCTGACATCAGGT[A/G]ATATGCCCGCCTTGG	7110
rs564203220	in-del	-/A	0.00159617	0.0282053	intron-variant	TMF1	GRCh38.p7	3:69030395	TATAAAACTTTTAGG[-/A]AAAAAACAGAGGAGA	7110
rs564206778	snp	A/C	0.000399281	0.0141238	intron-variant, downstream-variant-500B	TMF1, MIR3136	GRCh38.p7	3:69048771	AACTGGTGTGGGTCC[A/C]CCTGAGAGGAAGGAG	7110
rs564270470	snp	C/G			intron-variant	TMF1	GRCh38.p7	3:69029299	TCAGCCTCCCAAAGT[C/G]CTGGATAACAGGCAT	7110
rs564370705	snp	G/T	0.000399281	0.0141238	synonymous-codon	TMF1	GRCh38.p7	3:69029955	AGCAAGGAGTTCTTC[G/T]GTAGCTGCACGTTCT	7110
rs564390836	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime	TMF1	GRCh38.p7	3:69020277	TTTAGAATATCTTAA[C/G]TCACAACATAGATAT	7110
rs564648083	snp	C/T	0.00199481	0.0315187	intron-variant	TMF1	GRCh38.p7	3:69029010	TGAATCCCAGTACTA[C/T]CTTCTTGTTATAATA	7110
rs564664589	snp	C/G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TMF1, MIR3136	GRCh38.p7	3:69049360	GCCTGGGTGACAGAT[C/G/T]GAGAACCTGTCTCGA	7110
rs564668706	snp	C/T	0.000798403	0.0199641	intron-variant	TMF1	GRCh38.p7	3:69042075	AAAGTCTCACTCTGT[C/T]GCCCAGGCTGCAGTA	7110
rs564727888	snp	C/T	1.6585e-05	0.00287962	synonymous-codon	TMF1	GRCh38.p7	3:69042874	AGTTTCACTACTATT[C/T]AATCTAGTGGCAAGT	7110
rs564828027	snp	A/T			intron-variant, downstream-variant-500B	TMF1, MIR3136	GRCh38.p7	3:69048606	GAACACATATATGTT[A/T]CATTAATATTTCAAT	7110
rs564907503	snp	A/G	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69045393	AACCCAGGAGGTGGA[A/G]GTTGCAGTGAGCCAA	7110
rs565013929	snp	A/C	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69031212	TTTAGAAACAGAGGA[A/C]AGATTAGTGATTGCC	7110
rs565060625	in-del	-/GATTATGTCT	0.00358779	0.0422022	intron-variant, upstream-variant-2KB	TMF1, MIR3136	GRCh38.p7	3:69050438	CAAATGAACAACCAA[-/GATTATGTCT]GATTAATTTAAATAC	7110
rs565320981	snp	C/T	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69031765	CTCTGCTCCACAGCA[C/T]AGCTATGGTCTTTTT	7110
rs565341762	snp	C/T	0.000798403	0.0199641	intron-variant	TMF1	GRCh38.p7	3:69037658	ACAAAAAAAGAAAAT[C/T]AGCCAGGCATGGTAG	7110
rs565487448	snp	C/T	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69034200	TTCTTTGGCCAGGCA[C/T]GGTGGCTCATGTGTG	7110
rs565569446	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69036726	TAAATCAAAAGGGCA[C/T]AGGAGTCAATAAAAA	7110
rs565595821	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69027157	CATGCCACCATGCCC[A/G]GCTAATTTTTGTATT	7110
rs565609092	snp	C/T	0.00478085	0.0486577	intron-variant, downstream-variant-500B	TMF1, MIR3136	GRCh38.p7	3:69048888	ATATGTTTTATAACC[C/T]ACAGTAAGTCCAAGA	7110
rs565737645	snp	C/T	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69029178	AGCTGGAATTACAGG[C/T]GTCTGCCACCATGCC	7110
rs565799521	snp	C/G	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69029677	ACCTCCTGACCTCAA[C/G]TGATCCGCCCGCCTT	7110
rs565838826	snp	A/C			utr-variant-3-prime	TMF1	GRCh38.p7	3:69022122	AAGAAGGCATAGCTA[A/C]TTTTAAAAGCTATTC	7110
rs565967914	snp	A/T			intron-variant	TMF1	GRCh38.p7	3:69033828	AAATAATTTGCTTTT[A/T]AATTATTATTATTAA	7110
rs565998810	snp	C/T	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69042174	CCTGAGTAGCTGGGA[C/T]TAGAGGCACGCACCA	7110
rs566199116	snp	A/G	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69037511	GCCGGGCATGGTGGT[A/G]GGCACCTGTAATCCC	7110
rs566243995	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69031114	AACCTCTTCCTGGGA[A/G]TTACACTGAGTGAAA	7110
rs566283008	snp	A/T			intron-variant	TMF1	GRCh38.p7	3:69027767	CATTCAAAATCATCC[A/T]GGGCCACATGCCAAC	7110
rs566435186	snp	C/T	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69024459	TATATTTTTCTAATC[C/T]AAGGAAATGACATAT	7110
rs566623608	snp	A/C			intron-variant	TMF1	GRCh38.p7	3:69051489	CAACAACAACATAAA[A/C]CCACATTACGCGCTA	7110
rs566636712	in-del	-/AGAG			intron-variant	TMF1	GRCh38.p7	3:69046091	GCTAGCCTGGACAAT[-/AGAG]AGAGACCCTGTCTCA	7110
rs566735075	snp	A/C	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69045307	TACTGAAAATACAAA[A/C]ATTAGCTGGGCATGG	7110
rs566735309	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	TMF1	GRCh38.p7	3:69052504	CTACCGATAGAGGTC[G/T]ATTTCCCCGGAAGGA	7110
rs566937883	snp	A/T	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69026178	ATTTCCTAGGGTTAA[A/T]GAGAACAAAGATTCA	7110
rs567085559	snp	C/G	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69039332	ATCTCAAACTCCTGG[C/G]CTCAAGTGATCTGCC	7110
rs567177283	snp	A/C	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69037485	TCTCTACTAAAAAAA[A/C]ACAAAAATTAGCCGG	7110
rs567238650	snp	C/T	0.0023933	0.0345097	intron-variant	TMF1	GRCh38.p7	3:69030356	ACTCAAAATGGATCA[C/T]AGACTTATATGTAAA	7110
rs567313035	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69038322	CTTCTAAGAGGGTTC[C/T]TAGCTTTTATAATAC	7110
rs567341805	snp	C/T	0.000798403	0.0199641	intron-variant	TMF1	GRCh38.p7	3:69044010	ACAGTTTTAGGCCTA[C/T]TAACTTTTAAGAAAA	7110
rs567353651	snp	C/T			utr-variant-3-prime	TMF1	GRCh38.p7	3:69022621	TTCAGACAGTGTCAG[C/T]GTGACTCTTACTTTT	7110
rs567458856	snp	A/G	0.00159617	0.0282053	intron-variant	TMF1	GRCh38.p7	3:69042076	AAGTCTCACTCTGTC[A/G]CCCAGGCTGCAGTAC	7110
rs567600502	snp	A/T	0.0174175	0.0916809	intron-variant	TMF1	GRCh38.p7	3:69040937	AAAAAAAAAAAAAAA[A/T]TTTTTCTGGGGCACG	7110
rs567756306	snp	A/G	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69025372	TAGCAGGTTCAGTTG[A/G]CTGTTATCCTTAGCT	7110
rs567778220	snp	A/G	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69033045	TCCTACACTACTGCA[A/G]ACAAGCTACAAAGGG	7110
rs567830712	snp	A/G	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69051860	CTCTCAGCAAGGAAG[A/G]ACCCCTCTCTACACC	7110
rs567850949	snp	C/T	0.00318978	0.0398085	intron-variant	TMF1	GRCh38.p7	3:69051397	GGAGAATCGCTAGAA[C/T]CTGGGAGGCGGAGGT	7110
rs567893214	snp	C/G	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69045226	ACTTTGGGAGGCTGA[C/G]GTGGGGGGATCACCT	7110
rs567916035	snp	C/G	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69044799	ACAACCAAATAGCTA[C/G]TGGGAGTGTAAGTTG	7110
rs568034133	snp	C/T	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69046793	CTATCAATAGGAGAT[C/T]TCAAAAATAACATAA	7110
rs568081930	snp	A/T			intron-variant, upstream-variant-2KB	TMF1, MIR3136	GRCh38.p7	3:69050903	CACATCAAATGCTGA[A/T]CTGTTCCTTAGACTT	7110
rs568095492	snp	G/T	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69039960	AGAAAAATCTGGCAG[G/T]CAACTCCTTAACTAA	7110
rs568108504	snp	C/T	0.000798403	0.0199641	intron-variant	TMF1	GRCh38.p7	3:69028064	AGTCAATCTCAAAGT[C/T]AGAAGCATAAAGTAT	7110
rs568158325	snp	A/G	8.28123e-05	0.00643423	missense	TMF1	GRCh38.p7	3:69026055	TTATTGAACTTGAGC[A/G]TGACATGGTGGGAGT	7110
rs568177626	snp	C/T	1.76552e-05	0.00297108	missense	TMF1	GRCh38.p7	3:69047359	CTTACTAGAGTTACC[C/T]TGCAAACATCTTCCT	7110
rs568370857	snp	A/G	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69034463	GGGCAACAGAGCAAG[A/G]CTCTGTCTCAAAATA	7110
rs568409510	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	TMF1	GRCh38.p7	3:69052565	GGAAAATAGTTCACG[C/T]GCTAAAAGCTTGCAC	7110
rs568421862	snp	A/G	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69027331	AAATTACCCTCATTA[A/G]CCAGAAAGAAAACAA	7110
rs568474492	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	TMF1	GRCh38.p7	3:69020555	TCCTATCCATTAAAA[C/T]ATAAATATTATTTTG	7110
rs568631256	snp	C/T	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69040550	CAAGATGTTAACACC[C/T]GATGAATCTAGGTGA	7110
rs568822772	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	TMF1	GRCh38.p7	3:69052517	TCGATTTCCCCGGAA[A/G]GAATATTCAAGTTTT	7110
rs568836296	snp	C/G	0.000399281	0.0141238	utr-variant-5-prime	TMF1	GRCh38.p7	3:69052275	CCGCACAGCTGAGAC[C/G]AAGGGGGCCCATGTG	7110
rs568886563	snp	A/G	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69034245	TGGGAGGCTGAGGTG[A/G]GTGGATCACCTGAAG	7110
rs568929420	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69047288	ATGCATCAATGAAAG[C/T]ATTTTTTAAAACAAA	7110
rs569019981	snp	A/T	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69025150	GTAGCTGGAACAACT[A/T]ATCTAAGAGGTAAAT	7110
rs569099971	snp	A/G	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69039361	CCTGTCGCAGCCTCC[A/G]AAAGTGTTGGGATTA	7110
rs569156890	snp	C/T	0.00358779	0.0422022	intron-variant	TMF1	GRCh38.p7	3:69026724	CAACAATGTAATTTG[C/T]TGGGTTTTTATAATA	7110
rs569157607	snp	A/T	0.000798403	0.0199641	intron-variant	TMF1	GRCh38.p7	3:69039830	ACAATGTTACAACTA[A/T]TTTGGACAGCAATCA	7110
rs569271740	snp	C/G	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69027202	GGTTTTGCCATGTTG[C/G]CCAGGCTGGTCTTGA	7110
rs569720939	snp	C/T	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69035362	CAAATATGTATAAGG[C/T]ATAGCCATTACCATA	7110
rs569756433	snp	G/T	0.000399281	0.0141238	downstream-variant-500B, upstream-variant-2KB	UBA3, TMF1	GRCh38.p7	3:69054294	GCCGAGGGGGGCGGG[G/T]GGGGGTGGATCACCT	7110
rs569817813	snp	A/G	0.00112588	0.0236997	missense	TMF1	GRCh38.p7	3:69047459	GTCCTTCATTTATTG[A/G]TGTGGAAGAAACCAA	7110
rs570083202	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TMF1, MIR3136	GRCh38.p7	3:69050610	GTAAAACCTATATTC[A/T]ATCTTATCTAAAGTT	7110
rs570101907	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	TMF1, MIR3136	GRCh38.p7	3:69049986	GACTTCAGGCCAGGC[A/G]CAGTGGCTCACGCTT	7110
rs570209311	snp	G/T	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69029048	ACTTTATTTATTTTT[G/T]TTTTTTTGGAGACGG	7110
rs570277367	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	TMF1	GRCh38.p7	3:69022022	AGTAAAGGCAGTTAA[A/G]TAACTTTCAGTAATA	7110
rs570316215	snp	A/C			intron-variant	TMF1	GRCh38.p7	3:69036297	TATAATCTATCAATA[A/C]GAAAGAGCTGAAAAT	7110
rs570484259	snp	A/G			utr-variant-3-prime	TMF1	GRCh38.p7	3:69021350	CTACTATATTTTCTA[A/G]TTCTATACATTTCTT	7110
rs570488254	snp	C/T	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69034654	AAATTGTATTTTCTC[C/T]CCCTTTTCCTCTGCA	7110
rs570504697	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime	TMF1	GRCh38.p7	3:69021254	TATAGGAAAAAACAG[A/T]GTATAGAGGTGTCTA	7110
rs570520706	snp	A/T			intron-variant	TMF1	GRCh38.p7	3:69023779	AATCAACAAAATATT[A/T]CTAAGATCATACAAA	7110
rs570534509	snp	C/G	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69040674	GCTCACGCCTGTAAT[C/G]CCAGCACTTTTGGGA	7110
rs570544698	snp	C/T	3.39098e-05	0.00411749	synonymous-codon	TMF1	GRCh38.p7	3:69028238	TACCTTTTCTTTCCT[C/T]GTCTCTTCAAGTGTT	7110
rs570648430	in-del	-/TC	0.00199481	0.0315187	utr-variant-3-prime	TMF1	GRCh38.p7	3:69022914	GGATAAAGTAATAAA[-/TC]TCTGTGCTATTCAAG	7110
rs570689162	snp	A/G	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69027392	CAAATGATGTGCACT[A/G]GTTTCAGTGACAGAC	7110
rs570744969	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	TMF1	GRCh38.p7	3:69053437	GGTCACCAAATAATT[C/T]TCACTCACTCCAGTT	7110
rs570773242	snp	A/G	0.00597247	0.0543191	downstream-variant-500B, upstream-variant-2KB	UBA3, TMF1	GRCh38.p7	3:69054282	GCACTTTGGGAAGCC[A/G]AGGGGGGCGGGGGGG	7110
rs570915882	in-del	-/A	0.0019972	0.0315375	intron-variant	TMF1	GRCh38.p7	3:69035767	ATGTATAAAACATGT[-/A]AAAAAAATTTCTAAT	7110
rs571021994	snp	A/T	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69035292	CAATTCTAAAACTGT[A/T]TGTATATTCAATGTT	7110
rs571090110	snp	A/C/T	0.000104177	0.00721663	intron-variant	TMF1	GRCh38.p7	3:69028213	AGAGCTGAGTGGTCA[A/C/T]GAAGAGAAATACCTT	7110
rs571119294	snp	C/T	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69042396	TAATTTAAAAATTAA[C/T]ACAATGAAAAATTCA	7110
rs571215343	snp	C/T	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69030163	GTCTACTGAGACAAA[C/T]GAACCAATCTTAACT	7110
rs571329468	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	TMF1	GRCh38.p7	3:69022200	TCACAAAATTAAAAA[C/T]GCCAAATTCAAGTTA	7110
rs571425605	snp	C/T	0.00199481	0.0315187	intron-variant	TMF1	GRCh38.p7	3:69036250	ATAAACTATCATTTA[C/T]GTAAAAAGGATGTAG	7110
rs571555361	snp	C/T	0.000798403	0.0199641	intron-variant	TMF1	GRCh38.p7	3:69036989	GAAAAAGAAAGACAA[C/T]CCACAGAGAGGCACA	7110
rs571657867	snp	C/T	1.79303e-05	0.00299413	intron-variant	TMF1	GRCh38.p7	3:69044646	AGCTTTAAAAAAGAC[C/T]ATTTTTACATGCAGG	7110
rs571721331	snp	A/G	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69038155	CCCATATGCCCATCA[A/G]CTGATGATTTGATAA	7110
rs571727513	snp	A/C	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69031505	GTATCAATGTCAATA[A/C]CATGGTTGTGATATT	7110
rs571806282	snp	C/G	0.000514698	0.0160338	intron-variant	TMF1	GRCh38.p7	3:69038733	TCTCTTAAAAAATTA[C/G]ATTGAGTTTATAAAT	7110
rs571839250	snp	A/T			intron-variant	TMF1	GRCh38.p7	3:69031185	TATGTAACATTTTTG[A/T]AATGACAGAATTTTA	7110
rs571874838	snp	C/G	0.000798403	0.0199641	intron-variant	TMF1	GRCh38.p7	3:69051365	CTGTAATCCCAGCTA[C/G]TAGGGAGGCTGGGGA	7110
rs571915884	snp	G/T	0.000798403	0.0199641	intron-variant	TMF1	GRCh38.p7	3:69028648	AATGTTTCTAAAAGT[G/T]CAGATATTTTACTTT	7110
rs571925873	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	TMF1	GRCh38.p7	3:69020046	GAACATAAATGTATA[C/T]GTACTAAACATACAG	7110
rs571951367	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69028951	CCCTGGAAAAAAAAA[C/T]AAATACAAAACATGC	7110
rs571962341	snp	C/T			utr-variant-3-prime	TMF1	GRCh38.p7	3:69020454	CAAACAACCTTCCCT[C/T]TGTTTACTCATTTTT	7110
rs572282999	snp	C/T	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69035460	TACGGATTATAAAAG[C/T]TGGGGGCTCCACTCA	7110
rs572388762	in-del	-/A			intron-variant	TMF1	GRCh38.p7	3:69027681	ATAGCTGATGAACTA[-/A]AAAAAAAAAAAAAAA	7110
rs572411022	snp	A/C	0.0023933	0.0345097	intron-variant	TMF1	GRCh38.p7	3:69027628	GCCTCATTTGAAGAA[A/C]AAGAATTGTCTTGGG	7110
rs572414169	snp	C/T	0.000798403	0.0199641	intron-variant	TMF1	GRCh38.p7	3:69036491	AAATAGGTGTATAAG[C/T]GAATGTGTATGTACG	7110
rs572419761	snp	A/G	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69037170	GGCCAATAAGCAAAT[A/G]AAAAGACATCCAACA	7110
rs572588556	snp	A/G	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69044333	GTAAAGACAATCAAA[A/G]GAGAAAAGTAATCTT	7110
rs572590622	snp	A/G	0.0023933	0.0345097	intron-variant	TMF1	GRCh38.p7	3:69051424	AGGTTGCAGTGAGCC[A/G]AGATCGCGCCACTGC	7110
rs572652412	snp	C/T	0.00199481	0.0315187	intron-variant	TMF1	GRCh38.p7	3:69044869	GGGATCTACATACTC[C/T]TTGATATAGAAAATT	7110
rs572704882	snp	C/T	6.62405e-05	0.00575464	missense	TMF1	GRCh38.p7	3:69048422	AGGCACTGAAGAAAT[C/T]TTCAGATTCATCGAC	7110
rs572747641	snp	C/T	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69042586	TTTTACAGGGACTTA[C/T]TTTTCTTTTTACTTC	7110
rs572943280	snp	A/G	0.0023933	0.0345097	intron-variant	TMF1	GRCh38.p7	3:69037700	AGTCCCAGCTACTCA[A/G]GAGGCTGAGGCAGAA	7110
rs573054459	snp	A/G			upstream-variant-2KB	TMF1	GRCh38.p7	3:69052481	TCTTAGCGAAGGGGA[A/G]GCTATGGCTACCGAT	7110
rs573083261	snp	A/T			intron-variant	TMF1	GRCh38.p7	3:69043003	CAAAGAAGCTGTCCA[A/T]AATCACATTTGCAAT	7110
rs573320577	snp	C/T	1.66032e-05	0.0028812	intron-variant	TMF1	GRCh38.p7	3:69038731	GTTCTCTTAAAAAAT[C/T]AGATTGAGTTTATAA	7110
rs573430907	snp	G/T	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69031706	TTCTTGTATTTTTTC[G/T]CCACCAAAGTAGAGC	7110
rs573516049	snp	G/T	0.000798403	0.0199641	intron-variant	TMF1	GRCh38.p7	3:69032460	AGGCATACATGAATT[G/T]TTCATGAATTTGCTA	7110
rs573664056	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TMF1, MIR3136	GRCh38.p7	3:69050266	CTGTGTCTCAAAAAA[A/C]AAAAAAACAAAAAAA	7110
rs573861707	snp	C/T			missense	TMF1	GRCh38.p7	3:69052073	GAGAGCTGGGAGGCG[C/T]TGAACCAACTCATCG	7110
rs574020936	snp	A/G	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69024685	CTTTAATATTTTCAT[A/G]TAACTAAAAGTATAT	7110
rs574054509	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69035755	AAATTACAATAAATG[C/T]ATAAAACATGTAAAA	7110
rs574156933	snp	A/T	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69044241	CAAATACGTTTTAAA[A/T]CTCTAATACTAAAAG	7110
rs574188591	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69036772	CTGGTCCTGCAACAA[C/T]TGGATATCCACATGC	7110
rs574224415	snp	C/T	0.00279162	0.0372561	intron-variant	TMF1	GRCh38.p7	3:69033265	AGTGAAAGAGTGAGA[C/T]TCCATCTCAAAAAAA	7110
rs574355415	snp	C/T	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69039092	AGGAATCTATAATAA[C/T]GGAGAAAAATATATA	7110
rs574429155	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime	TMF1	GRCh38.p7	3:69022151	TCTATGCTTTCCTTG[A/T]GTTTGAAATTTCAAG	7110
rs574438409	snp	A/C			upstream-variant-2KB, utr-variant-5-prime	TMF1	GRCh38.p7	3:69052335	GCAACCAAATCTACG[A/C]GCCCAGAGTTCGGTC	7110
rs574672673	snp	C/T	0.000798403	0.0199641	intron-variant	TMF1	GRCh38.p7	3:69026448	CTAAAAATACAAAAT[C/T]AGCTGGGCGTGGTGG	7110
rs574689796	snp	A/C	0.000798403	0.0199641	intron-variant	TMF1	GRCh38.p7	3:69045573	TCACTTGAGGTCAGG[A/C]GTTCAAGACCAGCCT	7110
rs574768008	snp	G/T	0.000798403	0.0199641	utr-variant-5-prime	TMF1	GRCh38.p7	3:69052301	ATGTGCGCATGCGCT[G/T]GCTTCTTCCACGTAC	7110
rs574768414	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69047245	GAAATGGCAAAATGC[A/G]TATGTTTTTAAATCT	7110
rs574821078	snp	A/C	0.00119737	0.0244387	intron-variant	TMF1	GRCh38.p7	3:69047106	GACTCAAAAATAAAG[A/C]TGTAAGATGAAAACT	7110
rs574882003	snp	C/T	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69040370	AATTAATGCTGATTT[C/T]TTAGGTTTGACTATG	7110
rs574905922	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69044130	AAAAATAAGAGAAGA[A/G]TAAATACAATGTTTC	7110
rs574958593	snp	C/T	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69045455	GTGACAAGAGTGAAA[C/T]TCCATCTCAAAAAGT	7110
rs574958756	snp	C/T	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69038446	TAGCAGAATCCAGTA[C/T]TCTGAAATCTAACAC	7110
rs575032355	in-del	-/AA	0.0004584	0.0151324	intron-variant	TMF1	GRCh38.p7	3:69024031	AAATATCTTAGACTC[-/AA]ATCCTTAGGTGAAGA	7110
rs575236725	snp	A/C			intron-variant, downstream-variant-500B	TMF1, MIR3136	GRCh38.p7	3:69048813	AAAGACTGGGCCTGG[A/C]CTGGACTACCAGATG	7110
rs575491960	snp	C/T	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69051480	ACTCCGTCTCAACAA[C/T]AACATAAAACCACAT	7110
rs575508437	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69043558	GTGATCCGCCCACTT[C/T]AGCCTCCCAGTGTGC	7110
rs575692547	snp	C/T	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69046289	GGAAGGGTTCCTTTT[C/T]GGACTCAAAAAAATA	7110
rs575739572	snp	A/G	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69032667	CCAGGCTGGAGTGCT[A/G]TAGCGCAATCTCAGC	7110
rs575820380	snp	C/T	5.00622e-05	0.00500286	synonymous-codon	TMF1	GRCh38.p7	3:69025707	TGAGTGATCATGAGA[C/T]TCATCCTATGTTAAT	7110
rs575847278	snp	A/G	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69033193	GCAGGAGAATTGTGT[A/G]AACCTGGGAGGCGGA	7110
rs575916121	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69039264	CTAATTTTTGTATTA[A/G]GTTGGTGCAGTATTT	7110
rs575956932	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69028629	TATTAGGGAGTTCTA[C/T]GAAAATGTTTCTAAA	7110
rs576059874	snp	C/T	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69027465	AAGTCCTAGAAATCA[C/T]AGATCTCTTTGGATA	7110
rs576098555	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	TMF1	GRCh38.p7	3:69019808	CCACTATAAATTTTG[C/T]TAAAAATGAAATACA	7110
rs576192210	snp	C/T	0.000798403	0.0199641	intron-variant	TMF1	GRCh38.p7	3:69047062	AAATTGACATACTAA[C/T]AAGCATAACAGAATT	7110
rs576198429	in-del	-/AAAT	0.00716266	0.059414	utr-variant-3-prime	TMF1	GRCh38.p7	3:69022953	AATGAATGCTTTAAA[-/AAAT]AAATCTTTAAAGAAT	7110
rs576307374	snp	A/G	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69039496	TAACCATGGCCAACT[A/G]TTCATACAGGAAGTA	7110
rs576362694	snp	C/T	0.00318978	0.0398085	intron-variant, upstream-variant-2KB	TMF1, MIR3136	GRCh38.p7	3:69049250	CTGGTGGCCCACATA[C/T]GTGGTCCCAGCTACT	7110
rs576371207	snp	C/G	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69040162	TGTGGGACAACTGCC[C/G]TAGACTCTACAGAGT	7110
rs576425259	snp	C/T	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69042545	CCTGTTTAAAGTTTT[C/T]TTAGGGCAGCACAAA	7110
rs576479720	snp	A/G	0.000798403	0.0199641	intron-variant	TMF1	GRCh38.p7	3:69026561	AGCGGTGGAGGTGGC[A/G]GTGAGCTGAGATAGC	7110
rs576624976	snp	C/G			utr-variant-3-prime	TMF1	GRCh38.p7	3:69021769	CATTGTAACCTCCAC[C/G]TCCCAGGTTCAAGCA	7110
rs576678341	snp	C/T	0.00119737	0.0244387	intron-variant	TMF1	GRCh38.p7	3:69045290	CGGTGAAAACCAGTC[C/T]CTACTGAAAATACAA	7110
rs576715531	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	TMF1, MIR3136	GRCh38.p7	3:69048658	ATATAAATTTAGAAA[A/G]AATACCCTATGAAAT	7110
rs576739752	snp	A/C			intron-variant	TMF1	GRCh38.p7	3:69023679	CACACCACAGGAAAG[A/C]TCAAAAGAAAACATA	7110
rs576775354	snp	A/G	0.000798403	0.0199641	intron-variant	TMF1	GRCh38.p7	3:69033377	TGGTTTGAAAGAGAC[A/G]TAATAAAGGTATTAA	7110
rs576784960	snp	C/T	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69040042	GCTGATGTGATATAG[C/T]TGTTCAATATCACCC	7110
rs576797382	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69032568	TTTATTAACATCACA[A/G]AAGGGCAACCTGGGG	7110
rs576829246	snp	A/G	3.31329e-05	0.00407005	missense	TMF1	GRCh38.p7	3:69047614	GTTTTAGACTTTGGA[A/G]TTGAAGAATTAACTA	7110
rs576853135	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69029132	TCTGCCTCCCAGGTT[C/T]AAGCAATTCTCCTGC	7110
rs576890650	snp	C/T	0.00199481	0.0315187	intron-variant	TMF1	GRCh38.p7	3:69040839	AGGCAGGAGAATTGC[C/T]TGAACCTGGGAGGCG	7110
rs576951422	snp	C/G	0.0023933	0.0345097	intron-variant	TMF1	GRCh38.p7	3:69041689	ATGTAAGAGAAGGAA[C/G]ATTGGAAATTAAATA	7110
rs576986170	snp	C/T			missense	TMF1	GRCh38.p7	3:69047788	TGGAAATCATCTAAA[C/T]GATTATATTCAGGAC	7110
rs577070817	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69051570	ATGATTTACGTACTT[C/T]AGACCTTGGATCCCA	7110
rs577087237	snp	A/C	0.000798403	0.0199641	downstream-variant-500B	TMF1	GRCh38.p7	3:69019662	GTCAAAAAAAAAAAA[A/C]AAAACTACACTTAAT	7110
rs577113943	snp	A/G	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69039406	CCCACTCGGCTAAAA[A/G]ATCTTATCATTTATC	7110
rs577133588	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	TMF1	GRCh38.p7	3:69052727	AGGATCACGTATGAA[C/T]ACTGTGTCCAACTCG	7110
rs577444637	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	TMF1	GRCh38.p7	3:69053869	CAGCTCTCAGATAGA[G/T]TCACCTTCTTACAAT	7110
rs577446571	in-del	-/TGTG	0.000798403	0.0199641	intron-variant	TMF1	GRCh38.p7	3:69024258	TATAAAAATATTTAA[-/TGTG]TGTGTGGTTTTTTTT	7110
rs577727935	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69033322	AATGACATGGAAGTA[C/T]TTTAGCCAGTATCTG	7110
rs577755661	snp	A/G/T	0.00119737	0.0244387	intron-variant	TMF1	GRCh38.p7	3:69035507	TTATAAACTACCATA[A/G/T]CCTTTTTGGAAAACG	7110
rs577809372	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69035400	GGAGAAAAGACAGTG[C/T]GTCTATAAATATTTG	7110
rs577843072	snp	G/T	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69028680	GAAATCATTTTTACT[G/T]GACATTTTTTTAAAA	7110
rs577849719	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TMF1, MIR3136	GRCh38.p7	3:69049373	ATCGAGAACCTGTCT[C/T]GAAAACAAACAAAAC	7110
rs577959064	snp	C/T	0.000514262	0.0160271	missense	TMF1	GRCh38.p7	3:69029957	CAAGGAGTTCTTCTG[C/T]AGCTGCACGTTCTCT	7110
rs578007463	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	TMF1	GRCh38.p7	3:69020998	TTGTAACTTAAGTTT[C/T]ATATAGAGTAGTCTC	7110
rs578042406	snp	A/T	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69023975	ATAAATCACTAACAC[A/T]TACTATAAATTAAAA	7110
rs578060408	snp	A/G	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69037607	AGATTGCGCTATTGC[A/G]CTCCAGCCTGGGCAA	7110
rs578217863	snp	C/T	2.10804e-05	0.0032465	intron-variant	TMF1	GRCh38.p7	3:69042958	AAGAATGACTTTCAC[C/T]CTAAGTACAGTTCTC	7110
rs578240569	snp	A/G	0.000399281	0.0141238	intron-variant	TMF1	GRCh38.p7	3:69043601	CATGAGCCACCACAC[A/G]TGGCCAAAAATCTAC	7110
rs578245247	snp	A/G			synonymous-codon	TMF1	GRCh38.p7	3:69052075	GAGCTGGGAGGCGTT[A/G]AACCAACTCATCGCC	7110
rs745445454	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69040783	AAAAACTAGCTAGGC[A/G]TGGTGGCAGGTAGCT	7110
rs745450060	snp	A/C	1.66955e-05	0.0028892	intron-variant	TMF1	GRCh38.p7	3:69042771	CTTTTCCTGTTCTTA[A/C]AGTATTTTTCATAGT	7110
rs745516372	snp	C/T	1.67139e-05	0.00289079	intron-variant	TMF1	GRCh38.p7	3:69039712	GTGATGGTAAAGAAG[C/T]ATAAACTCAAATGAT	7110
rs745528615	snp	C/T			upstream-variant-2KB	TMF1	GRCh38.p7	3:69053302	GTCTGCAGCTATATT[C/T]GGTTTGGGCCCAAGT	7110
rs745582270	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69039975	TCAACTCCTTAACTA[A/G]GCATTCAGTTTTGGC	7110
rs745641858	snp	A/G	3.34381e-05	0.00408876	missense	TMF1	GRCh38.p7	3:69047408	GCTGACTTTCAGCAG[A/G]TTCACACTGCTCAGC	7110
rs745695301	snp	C/T	1.65616e-05	0.00287759	missense	TMF1	GRCh38.p7	3:69047507	AGTTAACAGGAGTTG[C/T]ACTTCGTCCACTTTC	7110
rs745778612	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69034083	CTCCCAAAGCATTGG[A/G]ATTATAGGCATGAAC	7110
rs745782471	snp	C/T	1.65902e-05	0.00288008	missense, downstream-variant-500B	TMF1, MIR3136	GRCh38.p7	3:69048505	CTCTGAGGTTCAGTG[C/T]TTGATTTCAACCCCC	7110
rs745792738	snp	C/T	1.6582e-05	0.00287936	missense	TMF1	GRCh38.p7	3:69033685	AGTTCCTGGTTTCGA[C/T]TCTCTGCTTCCTGGA	7110
rs745797445	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69045023	AAAGAAGAAGGGAGA[C/T]GGATGCAATCAAAAG	7110
rs745834535	snp	A/T	0.000182266	0.00954461	missense	TMF1	GRCh38.p7	3:69025636	CTTGATCCTGCTCCC[A/T]TCCTTACAGCATCAT	7110
rs745889262	snp	C/T	0.000236972	0.0108826	intron-variant	TMF1	GRCh38.p7	3:69023359	TTTTTAAAATAACTA[C/T]ACAGAACATCTTTAA	7110
rs745914483	in-del	-/AA	2.19522e-05	0.00331295	intron-variant	TMF1	GRCh38.p7	3:69028008	CTAATAGAGAGAAAT[-/AA]AGTTAGACAATTTCT	7110
rs745925179	snp	G/T			intron-variant	TMF1	GRCh38.p7	3:69038163	CCCATCAACTGATGA[G/T]TTGATAAGACAAAGC	7110
rs745945971	snp	A/T	3.31203e-05	0.00406928	synonymous-codon	TMF1	GRCh38.p7	3:69048288	AGTTCTTGACTGGCC[A/T]ATGTGCAAGGATTCA	7110
rs745986945	snp	G/T	1.7318e-05	0.00294256	intron-variant	TMF1	GRCh38.p7	3:69043905	AATATTTGAGAATGA[G/T]GATGGTGTCTATATA	7110
rs746099056	snp	G/T			intron-variant	TMF1	GRCh38.p7	3:69029431	ACGACATACTTTGTT[G/T]ATTTACTTATTTAAT	7110
rs746120702	snp	C/T	1.76083e-05	0.00296712	synonymous-codon	TMF1	GRCh38.p7	3:69023210	TAAAAGTTCATCTAT[C/T]TGAGTTTTGTACATA	7110
rs746127092	snp	A/G	3.58699e-05	0.00423482	intron-variant	TMF1	GRCh38.p7	3:69030023	CTGATTACAGGACAG[A/G]AAAAAAAATCACATA	7110
rs746290752	snp	A/T			intron-variant, upstream-variant-2KB	TMF1, MIR3136	GRCh38.p7	3:69050784	CCTGACTTTTCAATG[A/T]TGTAAAATTAAGAAC	7110
rs746297689	snp	C/G	2.04668e-05	0.00319891	missense	TMF1	GRCh38.p7	3:69027977	TTTCCATTTCTAACT[C/G]ACTATTCAACAATGT	7110
rs746320846	snp	A/G	0.000132624	0.00814213	intron-variant	TMF1	GRCh38.p7	3:69035143	AAACAATACATTCAC[A/G]AACAATGGTACAGTA	7110
rs746362274	snp	C/T	1.70429e-05	0.0029191	intron-variant	TMF1	GRCh38.p7	3:69026143	TAAAGAGCAAAGAGA[C/T]AAGCAGAGAAAGCAA	7110
rs746375788	snp	A/G	1.65726e-05	0.00287855	stop-gained	TMF1	GRCh38.p7	3:69038587	CTAATGTTTCTTGCT[A/G]CTGACGGGCTTCTTC	7110
rs746407861	snp	A/T			intron-variant, upstream-variant-2KB	TMF1, MIR3136	GRCh38.p7	3:69049483	CTAGAGAACAAATTC[A/T]TTTTCATCCACTTAA	7110
rs746449341	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69038245	ATGTTATGAATGAGC[C/T]CAGGAGTTAAATGGA	7110
rs746592428	snp	C/T	1.6808e-05	0.00289892	intron-variant	TMF1	GRCh38.p7	3:69039519	AGGAAGTAATAACAA[C/T]ATATATGTAGAGAAT	7110
rs746607109	snp	C/G			intron-variant	TMF1	GRCh38.p7	3:69028984	CACAATCTCAACAAT[C/G]TACATGACAATGAAT	7110
rs746638304	snp	G/T	3.35194e-05	0.00409372	intron-variant	TMF1	GRCh38.p7	3:69026119	GAGTAAAAAAAATTC[G/T]GTTCATATTAAAGAG	7110
rs746660016	snp	C/G			intron-variant	TMF1	GRCh38.p7	3:69036628	AGGAAATGGGGAGCA[C/G]CTAAATTGGAAGTAA	7110
rs746689513	snp	C/T	4.1148e-05	0.00453567	synonymous-codon	TMF1	GRCh38.p7	3:69027933	TTGAGTAAAAATGGC[C/T]TTCTTCCTTTCTTGT	7110
rs746796691	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69034215	CGGTGGCTCATGTGT[A/G]TAATCCCAGCACTTT	7110
rs746836393	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69024217	TAGTTTAAATCAAAA[C/T]ATATCTTTTTTAATA	7110
rs746843152	snp	A/G	1.706e-05	0.00292057	intron-variant	TMF1	GRCh38.p7	3:69044615	ATAAGGCGAATACAT[A/G]AAAGTCAGAACGCTT	7110
rs746897025	snp	A/G	4.9755e-05	0.00498748	missense	TMF1	GRCh38.p7	3:69039667	TGATGTTAGAATTGT[A/G]CAGCTGCTGTTTTGA	7110
rs746940972	snp	A/T			downstream-variant-500B	TMF1	GRCh38.p7	3:69019565	GCTAAGGCAGGAGGA[A/T]CACTTGAACCTGGGA	7110
rs747112278	snp	A/G	1.65778e-05	0.002879	synonymous-codon	TMF1	GRCh38.p7	3:69029922	CTGTGACTCCATGGA[A/G]GACATCTGAATTTTG	7110
rs747135809	snp	C/T	1.65767e-05	0.00287891	synonymous-codon	TMF1	GRCh38.p7	3:69048150	TGGCACCTTCATATC[C/T]GATTCTTTATTAACA	7110
rs747176028	snp	C/T	1.67973e-05	0.00289799	intron-variant	TMF1	GRCh38.p7	3:69038819	TTCATTCTAAATGGG[C/T]TGCATATTTGTTCAT	7110
rs747180967	in-del	-/TTC	4.6934e-05	0.00484405	intron-variant	TMF1	GRCh38.p7	3:69042589	TACAGGGACTTACTT[-/TTC]TTTTTACTTCCAAAA	7110
rs747220550	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69045122	GTATTATTCTTTACC[C/T]GAAACACATACCCTT	7110
rs747364855	snp	C/G			intron-variant, upstream-variant-2KB	TMF1, MIR3136	GRCh38.p7	3:69050813	ACAGAAACCAGAAAG[C/G]AGTAGTCAAGTACAT	7110
rs747414786	in-del	-/ATG	0.000294486	0.0121308	intron-variant	TMF1	GRCh38.p7	3:69028043	ATAGTAATTCATGCC[-/ATG]ATAAGTCAATCTCAA	7110
rs747428881	snp	C/G	1.85431e-05	0.00304486	intron-variant	TMF1	GRCh38.p7	3:69043716	ATCTATATCTCTATA[C/G]AGTTTAATTAATATT	7110
rs747430989	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69039447	AAAATCCTTCTTACA[C/T]GATATACCCCATTAA	7110
rs747471322	snp	G/T	1.65605e-05	0.0028775	missense	TMF1	GRCh38.p7	3:69048274	TCAGTTGTTTCAGGA[G/T]TTCTTGACTGGCCAA	7110
rs747472805	snp	A/G	1.65677e-05	0.00287812	intron-variant	TMF1	GRCh38.p7	3:69035122	GTCCCCCACCTGTAG[A/G]AGGAGAAACAATACA	7110
rs747513745	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69023930	TTTTTAAACTTCTTT[A/G]CTCAAATATTAGTAC	7110
rs747525969	in-del	-/CTTA			intron-variant	TMF1	GRCh38.p7	3:69043650	TGATATCCTTTTCAC[-/CTTA]CTTCTCTTTTTTCCA	7110
rs747570305	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69047338	CACATCTAAAAATCC[C/T]TTCCACTTACTAGAG	7110
rs747603788	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69038236	CTCCCACAGATGTTA[C/T]GAATGAGCTCAGGAG	7110
rs747747556	snp	A/T			intron-variant	TMF1	GRCh38.p7	3:69041466	ATGACTGCTTCCAAC[A/T]GTTCTCAAACGCTAC	7110
rs747758953	snp	C/G	1.68488e-05	0.00290243	intron-variant	TMF1	GRCh38.p7	3:69051926	CGGGAGCCAGGAACC[C/G]CGCTCCTCTCTCTCT	7110
rs747835809	snp	A/C	1.70432e-05	0.00291913	intron-variant	TMF1	GRCh38.p7	3:69025967	TTATTATTCTAAGAA[A/C]TAAGCACATATAAAA	7110
rs747839610	snp	C/G			intron-variant	TMF1	GRCh38.p7	3:69030775	CTAAAAGAAAAAACA[C/G]GGACGACATAAAATG	7110
rs747939196	snp	A/C			upstream-variant-2KB	TMF1	GRCh38.p7	3:69053790	TGTACAGTTACAGTT[A/C]CAAGACTTCTAATTG	7110
rs748028319	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69042098	CTGCAGTACAGTGGC[A/G]TGATCTTGGCTCACT	7110
rs748031337	snp	A/G	1.65897e-05	0.00288003	synonymous-codon	TMF1	GRCh38.p7	3:69047754	AGCATCAGATGAACA[A/G]CAACTCTCAGTGAGT	7110
rs748069966	snp	C/T	1.66164e-05	0.00288235	missense	TMF1	GRCh38.p7	3:69038936	AGATCTTTCTCTTGG[C/T]GTTCTACCATGGAAT	7110
rs748082705	snp	C/T	2.08893e-05	0.00323175	intron-variant	TMF1	GRCh38.p7	3:69039061	GAAATAATACCATGG[C/T]AAATAACTGTATTCC	7110
rs748083904	snp	C/G			intron-variant	TMF1	GRCh38.p7	3:69025216	CCTTTATTCTGTTGG[C/G]AAAGAGCTGCTTGAA	7110
rs748156142	snp	G/T			intron-variant	TMF1	GRCh38.p7	3:69051265	GTGGATCGCCTTAAG[G/T]CAGGAGTTCCACCAG	7110
rs748175304	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69046383	TCAAAAATATCTGAT[A/G]GTAATTAGTGCTGGT	7110
rs748194587	snp	C/T			utr-variant-3-prime	TMF1	GRCh38.p7	3:69020425	CAGTCTGTGCTTAAT[C/T]GTCTATAAATGACCA	7110
rs748234261	in-del	-/T	0.000186098	0.00964441	intron-variant	TMF1	GRCh38.p7	3:69042376	CAGAGACAAAAGTGC[-/T]TTAATAATTTAAAAA	7110
rs748236467	snp	C/T	1.6799e-05	0.00289814	intron-variant	TMF1	GRCh38.p7	3:69038811	TCTGATAATTCATTC[C/T]AAATGGGTTGCATAT	7110
rs748334862	snp	C/G	1.74211e-05	0.00295132	missense	TMF1	GRCh38.p7	3:69047369	TTACCTTGCAAACAT[C/G]TTCCTTCTCAGAAAG	7110
rs748358239	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69035568	CTCACATCCTTTCAC[C/T]GGGCCATCCTAGTCT	7110
rs748494359	in-del	-/TTAATTAAACTCTATAGAGATATAGAT	1.7184e-05	0.00293117	intron-variant	TMF1	GRCh38.p7	3:69043893	AAATTTAAAATAATA[-/TTAATTAAACTCTATAGAGATATAGAT]TTTGAGAATGAGGAT	7110
rs748495669	snp	C/T	6.72224e-05	0.00579713	intron-variant	TMF1	GRCh38.p7	3:69039521	GAAGTAATAACAATA[C/T]ATATGTAGAGAATTA	7110
rs748565493	snp	C/T	9.97656e-05	0.00706207	synonymous-codon	TMF1	GRCh38.p7	3:69048060	TGCTGTGAGAGACTG[C/T]GTAGACGTATTAGAT	7110
rs748582331	in-del	-/A	1.72734e-05	0.00293878	intron-variant	TMF1	GRCh38.p7	3:69028316	AACAAGGCAGAATTT[-/A]AAAAAAACAGAAAAT	7110
rs748616783	snp	C/T	1.65869e-05	0.00287979	intron-variant	TMF1	GRCh38.p7	3:69042800	GTCAACCAAATACTA[C/T]ACGCACCTTCTTCCA	7110
rs748692992	in-del	-/AG			intron-variant	TMF1	GRCh38.p7	3:69033409	AATACATGTAGAAAA[-/AG]AGAAAATGTAAAAAT	7110
rs748705424	snp	C/G	3.31664e-05	0.00407211	missense	TMF1	GRCh38.p7	3:69048140	AACTTACAGTTGGCA[C/G]CTTCATATCCGATTC	7110
rs748810761	snp	A/G	1.65737e-05	0.00287864	synonymous-codon	TMF1	GRCh38.p7	3:69025659	AGCATCATAAAGATT[A/G]CTTCCATTTGCTGAT	7110
rs748837400	in-del	-/C	1.66183e-05	0.00288251	frameshift-variant	TMF1	GRCh38.p7	3:69044559	ATAATAACTGAGCCT[-/C]CCTTTTTTCCAGCTT	7110
rs748855420	snp	A/G	1.69438e-05	0.00291061	intron-variant	TMF1	GRCh38.p7	3:69051902	CTGCATCAAGAGAAC[A/G]GCAGCCTCCGGGAGC	7110
rs748889586	snp	C/G	1.65636e-05	0.00287776	missense	TMF1	GRCh38.p7	3:69035025	CCTGTGACAGTACCT[C/G]CTGAAGTTCACCGAT	7110
rs748900609	snp	C/T	1.65996e-05	0.00288089	missense	TMF1	GRCh38.p7	3:69033697	CGATTCTCTGCTTCC[C/T]GGAGTCTCTGAATCA	7110
rs748901427	snp	A/C	3.32077e-05	0.00407465	intron-variant	TMF1	GRCh38.p7	3:69042791	TTTTTCATAGTCAAC[A/C]AAATACTATACGCAC	7110
rs749062344	snp	A/G	0.000152363	0.00872687	intron-variant	TMF1	GRCh38.p7	3:69044607	CTGTCTGGATAAGGC[A/G]AATACATAAAAGTCA	7110
rs749140650	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69030993	AGAGCTTGGAATCAG[C/T]CTGGACGTCCCTTGT	7110
rs749208621	snp	A/G	1.65641e-05	0.00287781	missense	TMF1	GRCh38.p7	3:69047548	GCTTCCTCAGTGGGT[A/G]TAACTAATGTTTCAT	7110
rs749208790	snp	C/T			missense	TMF1	GRCh38.p7	3:69044556	GAGATAATAACTGAG[C/T]CTCCCTTTTTTCCAG	7110
rs749221070	snp	G/T	1.72285e-05	0.00293495	intron-variant	TMF1	GRCh38.p7	3:69025949	ATTTGCATATTTCCT[G/T]TATTATTATTCTAAG	7110
rs749231601	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69043239	TAGTGGTACAATGAC[A/G]ACTCACCACAGCCTC	7110
rs749261735	snp	C/T	5.02449e-05	0.00501198	missense	TMF1	GRCh38.p7	3:69038843	TGTTCATTTTCTTAC[C/T]TGTATGCACTATCCA	7110
rs749305823	in-del	-/C			intron-variant	TMF1	GRCh38.p7	3:69025457	ATGCCACTATGTCAT[-/C]TTGTTTCTCAATTTG	7110
rs749366085	snp	G/T			intron-variant	TMF1	GRCh38.p7	3:69035646	CCCTACAGTATTAAA[G/T]AGGCTAGCAAAAACA	7110
rs749396514	snp	A/G	1.77439e-05	0.00297853	splice-donor-variant, missense	TMF1	GRCh38.p7	3:69047356	CCACTTACTAGAGTT[A/G]CCTTGCAAACATCTT	7110
rs749438309	snp	A/G	3.31351e-05	0.00407019	missense	TMF1	GRCh38.p7	3:69038593	TTTCTTGCTGCTGAC[A/G]GGCTTCTTCTTGGGC	7110
rs749483085	in-del	-/G			intron-variant	TMF1	GRCh38.p7	3:69032798	ATTTTTGGTAGAGAC[-/G]GGGGGTCTCATCATG	7110
rs749492783	snp	A/T	7.53116e-05	0.00613597	intron-variant	TMF1	GRCh38.p7	3:69023367	ATAACTACACAGAAC[A/T]TCTTTAATATTTATA	7110
rs749511014	snp	C/T			utr-variant-3-prime	TMF1	GRCh38.p7	3:69020561	CCATTAAAATATAAA[C/T]ATTATTTTGCAAGAA	7110
rs749540646	in-del	-/GG			intron-variant	TMF1	GRCh38.p7	3:69040456	GGAGCAGAATGTTAC[-/GG]GGTATTTGTAACCTC	7110
rs749560538	snp	C/G			intron-variant	TMF1	GRCh38.p7	3:69037228	AGCCGGGCGTAGTGG[C/G]TCACGCCTGTAATCC	7110
rs749640687	snp	A/T			intron-variant	TMF1	GRCh38.p7	3:69027303	GCTCAGCCTCAGAAA[A/T]CTCATTTCAGAAAAA	7110
rs749655632	snp	C/T	0.00013356	0.00817082	synonymous-codon	TMF1	GRCh38.p7	3:69047886	CTCTTGTCTCGAGCT[C/T]GCTGAGCTCTCACTT	7110
rs749708544	snp	A/G	0.000558503	0.0167015	intron-variant	TMF1	GRCh38.p7	3:69042322	AGATTACAGTCATAA[A/G]CCACCACACTCAGCC	7110
rs749747334	snp	A/C/T	6.62409e-05	0.00575471	missense	TMF1	GRCh38.p7	3:69048304	ATGTGCAAGGATTCA[A/C/T]GTAAGCTGCTTTTCA	7110
rs749777502	snp	C/T	2.10884e-05	0.00324711	synonymous-codon	TMF1	GRCh38.p7	3:69027990	CTGACTATTCAACAA[C/T]GTCTAATAGAGAGAA	7110
rs749829696	snp	G/T	3.36791e-05	0.00410346	synonymous-codon	TMF1	GRCh38.p7	3:69028250	CCTCGTCTCTTCAAG[G/T]GTTCTTACATATTCA	7110
rs749839125	snp	C/T	3.31829e-05	0.00407313	missense	TMF1	GRCh38.p7	3:69029882	GGGCTTGAAATCTAC[C/T]GTTTTCCTGTCTTAA	7110
rs749939727	in-del	-/TTA	3.44768e-05	0.00415177	intron-variant	TMF1	GRCh38.p7	3:69025948	ATTTGCATATTTCCT[-/TTA]TTATTATTATTCTAA	7110
rs750019352	snp	A/C	1.65963e-05	0.0028806	missense	TMF1	GRCh38.p7	3:69048101	TAGTTGTTTTCACAT[A/C]AATTACACTTTCAGA	7110
rs750048741	snp	A/G	1.66685e-05	0.00288686	intron-variant	TMF1	GRCh38.p7	3:69038770	AGTGATCAGATAATA[A/G]AAAAAGTATTTCTTC	7110
rs750068147	snp	C/G			upstream-variant-2KB	TMF1	GRCh38.p7	3:69053688	CAATTTAGTCATGTA[C/G]ACAAGTAGTACCAAG	7110
rs750111351	snp	C/G	1.6684e-05	0.00288821	missense	TMF1	GRCh38.p7	3:69047993	AAGGTGTATTGCTCT[C/G]CCTGTCTTCATGTTT	7110
rs750115675	snp	A/G	1.79748e-05	0.00299784	intron-variant	TMF1	GRCh38.p7	3:69028341	GAAAATGAAAAAGAT[A/G]CTAGTATAGACTATT	7110
rs750250286	snp	A/T			intron-variant	TMF1	GRCh38.p7	3:69026636	CAAAACAAACAAACA[A/T]AAAAAAAGTACAATA	7110
rs750301856	snp	C/T	1.65968e-05	0.00288065	missense	TMF1	GRCh38.p7	3:69051993	TGCTCGGCTCCTCTT[C/T]CTGGATGTCCAGAAC	7110
rs750304317	snp	A/G	1.68687e-05	0.00290414	synonymous-codon	TMF1	GRCh38.p7	3:69042901	AAGTTCTTCTTTTAT[A/G]TTTTTGATTTCCTAA	7110
rs750317404	snp	C/T			synonymous-codon	TMF1	GRCh38.p7	3:69047529	TCCACTTTCTTCCAT[C/T]TCTGCTTCCTCAGTG	7110
rs750406354	snp	C/T	8.50145e-05	0.0065192	synonymous-codon	TMF1	GRCh38.p7	3:69043783	CTCTTTGCAGGCTAG[C/T]TGAACTTTCTTTTCT	7110
rs750411190	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69046126	TCATACATACATCCA[C/T]CCACACTAAAAGTAA	7110
rs750476904	snp	A/G	1.69261e-05	0.00290908	intron-variant	TMF1	GRCh38.p7	3:69033532	CTGCATCGAGCATAA[A/G]AACTAAAGCAGTTAC	7110
rs750499315	snp	G/T			intron-variant	TMF1	GRCh38.p7	3:69051829	CGGGCCGGGGAGAAA[G/T]TACTTCCTGAAAACT	7110
rs750536810	snp	C/T	1.65603e-05	0.00287747	missense	TMF1	GRCh38.p7	3:69048389	TCTGAATGGTCTGGA[C/T]ATCAGTTGGCGAGAG	7110
rs750561259	in-del	-/ATG	1.67371e-05	0.0028928	intron-variant	TMF1	GRCh38.p7	3:69039723	GAAGTATAAACTCAA[-/ATG]ATAACTATTCCCTAA	7110
rs750565625	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69040406	CCTGTCAAGGAAAAC[A/G]TACTTGCCCTTGGGA	7110
rs750590071	snp	C/G	3.33172e-05	0.00408136	missense	TMF1	GRCh38.p7	3:69047837	GCTGAAAAGATGTCT[C/G]CATCAAGTGAAGACT	7110
rs750642388	snp	A/C	1.65704e-05	0.00287836	missense	TMF1	GRCh38.p7	3:69039611	GTTCAGCTTTGCAAC[A/C]ATATTTTCATTCTCC	7110
rs750815472	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69030523	TCTATGTGAAGAGGA[C/T]GAAAAGGCAAACTAC	7110
rs750843320	snp	A/G	1.65622e-05	0.00287764	missense	TMF1	GRCh38.p7	3:69038661	ATTTCACGGCTCAGA[A/G]CAGCTTCCTGTGCCT	7110
rs750845512	snp	A/C	1.65699e-05	0.00287831	missense	TMF1	GRCh38.p7	3:69047446	TCTAACACAGTCTGT[A/C]CTTCATTTATTGGTG	7110
rs750884923	snp	G/T	1.65647e-05	0.00287786	synonymous-codon, downstream-variant-500B	TMF1, MIR3136	GRCh38.p7	3:69048480	TGCTTTAGGAGAGGC[G/T]ATTGGTGGACTCTGA	7110
rs750896478	snp	A/C			intron-variant	TMF1	GRCh38.p7	3:69044110	GTCACCAATATCTGA[A/C]ATGTAAAAATAAGAG	7110
rs750924359	snp	C/G	1.7174e-05	0.00293031	missense, downstream-variant-500B	TMF1, MIR3136	GRCh38.p7	3:69048553	CCTCCACTGACAGGG[C/G]AACTTATTCCTTTAA	7110
rs751017885	snp	A/G	1.66927e-05	0.00288895	missense	TMF1	GRCh38.p7	3:69025568	CCAATACCTGTAAAT[A/G]AGTGATTTCCCCTTC	7110
rs751070995	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69037752	CAGAGGTTGCAGTGA[A/G]CTGAGATCGTGCCAC	7110
rs751091122	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69041129	TTCGATATTAATATT[C/T]CAAATAACTCTTTTA	7110
rs751189467	snp	C/T	1.8371e-05	0.00303071	intron-variant	TMF1	GRCh38.p7	3:69047325	AATCTCCAAAAAGCA[C/T]ATCTAAAAATCCCTT	7110
rs751219859	snp	C/G	0.00011753	0.00766492	intron-variant	TMF1	GRCh38.p7	3:69042645	TCTGTCTCAATATAT[C/G]TTATTCCTCATTCTT	7110
rs751252042	snp	C/T			upstream-variant-2KB	TMF1	GRCh38.p7	3:69053852	ATCTAAAACTATTTA[C/T]TCAGCTCTCAGATAG	7110
rs751328762	snp	C/G			intron-variant, upstream-variant-2KB	TMF1, MIR3136	GRCh38.p7	3:69049300	GATCATCTGAGCCCA[C/G]GAGGTGGAAGCTGCA	7110
rs751400878	snp	A/G	1.66949e-05	0.00288915	missense	TMF1	GRCh38.p7	3:69047977	GTACTAACAGGAGGA[A/G]AAGGTGTATTGCTCT	7110
rs751410162	snp	A/G	1.65803e-05	0.00287922	synonymous-codon	TMF1	GRCh38.p7	3:69042871	TGCAGTTTCACTACT[A/G]TTTAATCTAGTGGCA	7110
rs751412476	snp	C/T	1.65677e-05	0.00287812	missense	TMF1	GRCh38.p7	3:69033664	GTTGATGAAACACTT[C/T]GACTCAGTTCCTGGT	7110
rs751415367	in-del	-/A	1.67125e-05	0.00289067	intron-variant	TMF1	GRCh38.p7	3:69026108	CGTTCCTTAGGGAGT[-/A]AAAAAAATTCTGTTC	7110
rs751445739	snp	A/C	1.70772e-05	0.00292204	intron-variant	TMF1	GRCh38.p7	3:69028305	TGGTACCTATTAAAC[A/C]AGGCAGAATTTAAAA	7110
rs751498260	snp	A/G	2.17734e-05	0.00329943	intron-variant	TMF1	GRCh38.p7	3:69042638	ACGTATCTCTGTCTC[A/G]ATATATCTTATTCCT	7110
rs751510899	in-del	-/AA	3.36649e-05	0.0041026	intron-variant	TMF1	GRCh38.p7	3:69039517	ACAGGAAGTAATAAC[-/AA]TATATATGTAGAGAA	7110
rs751559934	snp	A/G			intron-variant, upstream-variant-2KB	TMF1, MIR3136	GRCh38.p7	3:69049162	AGTCATTTGAGTCCA[A/G]GAGTTCAAGACAAGC	7110
rs751569693	in-del	-/CTT	6.62427e-05	0.00575473	cds-indel	TMF1	GRCh38.p7	3:69048320	GTAAGCTGCTTTTCA[-/CTT]CTTCTTCTGGTCGTT	7110
rs751670647	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69040508	GGGTAGTGTATGTAT[A/G]TGCAGAAAGATATGG	7110
rs751675497	snp	C/T	1.74561e-05	0.00295428	utr-variant-5-prime	TMF1	GRCh38.p7	3:69052134	CACCAAGCGGGAAGG[C/T]CTCAGGCCTGGGGAA	7110
rs751708201	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69028522	GCATTTTATTTATTG[A/G]TGCTCTGGGTTAAGA	7110
rs751732796	snp	C/T	3.31472e-05	0.00407093	missense	TMF1	GRCh38.p7	3:69047710	CGGCTATCTAATGAC[C/T]GTACACTAAATGAGT	7110
rs751747249	snp	A/T	0.000647914	0.0179871	intron-variant	TMF1	GRCh38.p7	3:69039020	AGGACCTATATGTTA[A/T]AAAAACAGACAAAAG	7110
rs751800184	snp	C/G	1.65902e-05	0.00288008	missense	TMF1	GRCh38.p7	3:69024132	TTGTTAATTTAACTA[C/G]TTCTTCAGCCATTAT	7110
rs751871298	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69026742	GGTTTTTATAATAGA[A/G]TAAGAATGTTTCTGT	7110
rs751931528	snp	A/T	1.66161e-05	0.00288232	missense	TMF1	GRCh38.p7	3:69044550	TACTAAGAGATAATA[A/T]CTGAGCCTCCCTTTT	7110
rs751933294	in-del	-/A			downstream-variant-500B	TMF1	GRCh38.p7	3:69019649	GAGTGAGACTCTGTC[-/A]AAAAAAAAAAAAAAA	7110
rs751962703	snp	A/G	3.31285e-05	0.00406978	missense, downstream-variant-500B	TMF1, MIR3136	GRCh38.p7	3:69048478	ATTGCTTTAGGAGAG[A/G]CTATTGGTGGACTCT	7110
rs751976108	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69033734	TCTGAAGTCATTACC[A/G]ATGACAGCAATAAAA	7110
rs752024389	snp	A/T			upstream-variant-2KB	TMF1	GRCh38.p7	3:69052943	CCCTCATAAATGGGG[A/T]TAGTGCCCTTATAAG	7110
rs752077971	snp	C/T	1.68272e-05	0.00290057	missense	TMF1	GRCh38.p7	3:69030007	AAGGTCTGGGATTCA[C/T]CTGATTACAGGACAG	7110
rs752085857	snp	C/G	1.65605e-05	0.0028775	missense	TMF1	GRCh38.p7	3:69048350	GTTGTGATTTTGCTG[C/G]AGGTTTTGATACCAC	7110
rs752114256	snp	A/G			utr-variant-5-prime	TMF1	GRCh38.p7	3:69052252	CGGGATGTTACCCTC[A/G]GCCGTTCCCGCACAG	7110
rs752126049	snp	A/G	1.97955e-05	0.00314601	intron-variant	TMF1	GRCh38.p7	3:69023323	TTTGATCCAAATCCT[A/G]AAAAATGTATTTGTT	7110
rs752131340	snp	A/G	3.42853e-05	0.00414023	intron-variant	TMF1	GRCh38.p7	3:69033511	ATAAACAAGATGGAA[A/G]AGCTTCTGCATCGAG	7110
rs752183025	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69046101	ACAATAGAGAGAGAC[C/T]CTGTCTCATTCATAC	7110
rs752311118	snp	G/T	1.65982e-05	0.00288077	missense	TMF1	GRCh38.p7	3:69038564	TCATCCATTGCTTAC[G/T]TGAATGGCTAATGTT	7110
rs752341173	snp	C/T	3.7e-05	0.00430101	synonymous-codon	TMF1	GRCh38.p7	3:69023306	CAGAATAGTGTTGTA[C/T]CTTTGATCCAAATCC	7110
rs752343019	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69045789	AAGTAGGGCTGGACA[C/T]GGGTTCATGCTTATA	7110
rs752345720	snp	C/G			intron-variant	TMF1	GRCh38.p7	3:69032264	ACTAATCTAGTTCAC[C/G]CCCCCGATTCACAAG	7110
rs752428768	snp	C/T	1.66211e-05	0.00288275	missense	TMF1	GRCh38.p7	3:69044537	AGTGCTTTTTCCTTA[C/T]TAAGAGATAATAACT	7110
rs752463828	in-del	-/A	1.88156e-05	0.00306715	intron-variant	TMF1	GRCh38.p7	3:69039027	ATATGTTATAAAAAC[-/A]GACAAAAGTATTTTT	7110
rs752496751	in-del	-/ACAA	0.000278841	0.0118043	intron-variant	TMF1	GRCh38.p7	3:69027872	CTAAATGGTTACACC[-/ACAA]ACAAACAAAAACAAA	7110
rs752538965	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69031149	CCAAACCCAAAATGT[C/T]ATACACTGTATAATT	7110
rs752549801	snp	A/T	1.67049e-05	0.00289002	synonymous-codon	TMF1	GRCh38.p7	3:69047949	ACTGGTGGTAGAAGT[A/T]CCTGATGAAAAGGTA	7110
rs752549954	snp	C/G	1.65712e-05	0.00287843	missense	TMF1	GRCh38.p7	3:69039623	AACCATATTTTCATT[C/G]TCCTTGTCTTTAGCT	7110
rs752554571	snp	C/T			intron-variant, upstream-variant-2KB	TMF1, MIR3136	GRCh38.p7	3:69050394	CATTTGCACAATATC[C/T]AAACCAGAGAAAATC	7110
rs752639521	snp	A/G	3.33294e-05	0.00408211	missense	TMF1	GRCh38.p7	3:69047846	ATGTCTGCATCAAGT[A/G]AAGACTTGATTTTGA	7110
rs752648169	snp	A/T	1.65636e-05	0.00287776	missense	TMF1	GRCh38.p7	3:69038630	TAATGCTGCAGAAAG[A/T]TCTTCTTTAGCTTTC	7110
rs752650242	snp	C/G	2.20914e-05	0.00332343	missense	TMF1	GRCh38.p7	3:69027917	TTTCTTTTATTGTTT[C/G]TTGAGTAAAAATGGC	7110
rs752655739	snp	C/T			utr-variant-3-prime	TMF1	GRCh38.p7	3:69022590	TTTTTAAGTTTAAAT[C/T]ATTCACTCTTTAAAT	7110
rs752701615	snp	C/T	3.56576e-05	0.00422227	intron-variant	TMF1	GRCh38.p7	3:69028176	TGCTGCCATCCCCAA[C/T]CATTCTCTAATGTAT	7110
rs752747282	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69037904	TTAAAAACAGACAAT[A/G]ATAAATCTTGGCAAG	7110
rs752753542	snp	A/T	1.65688e-05	0.00287821	missense	TMF1	GRCh38.p7	3:69026015	GACAGAAAAGATGTC[A/T]GTAGTCCTGCCATAT	7110
rs752776857	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69028854	CCTTGTAATATAAAA[A/G]TAACTCCAAAGAGTA	7110
rs752787057	snp	A/T			intron-variant	TMF1	GRCh38.p7	3:69042500	GTTACACACTTTGAA[A/T]GTCTTGGTTTAAATG	7110
rs752930296	snp	C/T			intron-variant, upstream-variant-2KB	TMF1, MIR3136	GRCh38.p7	3:69049216	GTCCCTACAAAAAAA[C/T]TTTTTTAATTAGCTG	7110
rs752947169	snp	A/G	3.32138e-05	0.00407502	missense	TMF1	GRCh38.p7	3:69029966	CTTCTGTAGCTGCAC[A/G]TTCTCTCTCAACTGC	7110
rs752975636	snp	A/C	1.65614e-05	0.00287757	missense	TMF1	GRCh38.p7	3:69047468	TTATTGGTGTGGAAG[A/C]AACCAAGATATCAGG	7110
rs752985130	snp	C/G			intron-variant	TMF1	GRCh38.p7	3:69030022	CCTGATTACAGGACA[C/G]AAAAAAAAATCACAT	7110
rs753001272	snp	A/G	1.76459e-05	0.00297029	utr-variant-3-prime	TMF1	GRCh38.p7	3:69023175	AATTCAATTTTCACA[A/G]GTTAACTGAGACTTT	7110
rs753073898	snp	A/G	6.62416e-05	0.00575469	synonymous-codon	TMF1	GRCh38.p7	3:69048240	TGAAACACACAAAGA[A/G]GAGTCTTTTACTTGT	7110
rs753094855	snp	A/G			upstream-variant-2KB	TMF1	GRCh38.p7	3:69053120	ACCCAGTTTATGGCA[A/G]TTTGTTACAGCAGTC	7110
rs753116686	snp	A/G			downstream-variant-500B	TMF1	GRCh38.p7	3:69019344	AGCACTGTGTTTTCC[A/G]AAAACATATCTTCAT	7110
rs753154529	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69041488	AAACGCTACCCTTTC[C/T]CTGGAAATTTACTTA	7110
rs753172138	snp	A/T	1.76874e-05	0.00297378	missense	TMF1	GRCh38.p7	3:69039002	ACCTCTTCTTTGCCA[A/T]CAAGGACCTATATGT	7110
rs753208457	in-del	-/CA	1.66023e-05	0.00288113	frameshift-variant	TMF1	GRCh38.p7	3:69052003	CTCTTCCTGGATGTC[-/CA]GAACCCTGTCAATAG	7110
rs753242425	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69040668	GCAGTGGCTCACGCC[C/T]GTAATCCCAGCACTT	7110
rs753276792	snp	G/T	1.65784e-05	0.00287905	missense	TMF1	GRCh38.p7	3:69029902	TCCTGTCTTAAAAGA[G/T]AATTCTGTGACTCCA	7110
rs753290736	in-del	-/GG			utr-variant-3-prime	TMF1	GRCh38.p7	3:69020866	AAATTGAAAAGTTTA[-/GG]AATGAGTTTTATTGC	7110
rs753305971	snp	A/G	1.76627e-05	0.00297171	missense	TMF1	GRCh38.p7	3:69023262	AATCGAAGTTCTTCT[A/G]CCTCTTCTGCTTTTT	7110
rs753474704	snp	A/C			intron-variant	TMF1	GRCh38.p7	3:69033959	GCTGGGACTACAGGT[A/C]CACGCCACCACACCT	7110
rs753539370	snp	C/T	1.81714e-05	0.0030142	utr-variant-3-prime	TMF1	GRCh38.p7	3:69023133	TTAAATGTTTAGATA[C/T]TAAATGCTTACATTC	7110
rs753547284	snp	C/T	0.000189599	0.00973465	intron-variant	TMF1	GRCh38.p7	3:69042936	AAAGAAATCTGTGAA[C/T]ACCGTAAAGAATGAC	7110
rs753566303	snp	C/T	1.67573e-05	0.00289454	missense	TMF1	GRCh38.p7	3:69047405	CTGGCTGACTTTCAG[C/T]AGGTTCACACTGCTC	7110
rs753604745	snp	C/T	5.32666e-05	0.00516047	intron-variant	TMF1	GRCh38.p7	3:69027892	CAAACAAAAACAAAA[C/T]TCAATACCTTTTCTT	7110
rs753669553	in-del	-/GATTATATTCAG	1.66153e-05	0.00288225	cds-indel	TMF1	GRCh38.p7	3:69047789	GGAAATCATCTAAAC[-/GATTATATTCAG]GACAAGCAGATGCAG	7110
rs753701010	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69026457	CAAAATTAGCTGGGC[A/G]TGGTGGCGCATGCCT	7110
rs753701504	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69039104	TAATGGAGAAAAATA[C/T]ATATTTTTTTGAGAC	7110
rs753734674	snp	A/G	1.65798e-05	0.00287917	synonymous-codon	TMF1	GRCh38.p7	3:69047736	TGAGTCTATTCTTTC[A/G]AAAGCATCAGATGAA	7110
rs753795416	snp	C/T	1.65776e-05	0.00287898	synonymous-codon	TMF1	GRCh38.p7	3:69025605	CTTTAGCTGAGACTG[C/T]AGGTTTTCAATTATG	7110
rs753836179	snp	A/T	1.7051e-05	0.0029198	intron-variant	TMF1	GRCh38.p7	3:69038517	TAATTTGTAGAAGCA[A/T]AAACAAATATTTTTA	7110
rs753880976	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69024932	ATGTCAGCACTCAAA[A/G]TTTTGGATTTGGGGG	7110
rs754009480	snp	C/T	1.81952e-05	0.00301617	intron-variant, downstream-variant-500B	TMF1, MIR3136	GRCh38.p7	3:69048566	GGGAACTTATTCCTT[C/T]AACAAAAAAGTAAAT	7110
rs754027645	snp	A/C	1.65712e-05	0.00287843	missense, downstream-variant-500B	TMF1, MIR3136	GRCh38.p7	3:69048492	GGCTATTGGTGGACT[A/C]TGAGGTTCAGTGTTT	7110
rs754030755	snp	A/G	0.000135547	0.00823136	intron-variant	TMF1	GRCh38.p7	3:69042619	AAAAACAAAAGCTAG[A/G]AACACGTATCTCTGT	7110
rs754031694	snp	C/T	6.62559e-05	0.00575531	synonymous-codon	TMF1	GRCh38.p7	3:69033639	TATTTGTCGAAGCAA[C/T]GGTCTTGTTGTTGAT	7110
rs754061581	snp	A/G	3.33317e-05	0.00408224	synonymous-codon	TMF1	GRCh38.p7	3:69033555	GCAGTTACCAAGCCT[A/G]TCAGAAAGATTCTTC	7110
rs754073166	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69038125	TTATTGATAATAACC[A/G]CAAAGTATAAATAAC	7110
rs754097134	snp	C/T	1.66156e-05	0.00288228	missense	TMF1	GRCh38.p7	3:69038879	GCCTGAATACTTCGG[C/T]TCTTTTCTTCAAGTT	7110
rs754144981	snp	G/T	1.79319e-05	0.00299427	intron-variant	TMF1	GRCh38.p7	3:69029767	TTTTAAAAAGTGCTT[G/T]AGGATGTCACGGAAC	7110
rs754162760	snp	A/C			intron-variant, upstream-variant-2KB	TMF1, MIR3136	GRCh38.p7	3:69050519	ACTTTATATAATCCC[A/C]GGGTTATTTGGTATC	7110
rs754219033	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69041749	TAAAAAATACATTAA[A/G]ACTAGAAAAAATTAA	7110
rs754336188	snp	C/T	1.65649e-05	0.00287788	synonymous-codon	TMF1	GRCh38.p7	3:69047577	ATTTACTTCTTCAGA[C/T]TTTCCTTCAGCAGAT	7110
rs754344397	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69042566	GCAGCACAAATTTCT[A/G]TCTATTTTACAGGGA	7110
rs754351822	snp	C/T	1.65663e-05	0.002878	missense	TMF1	GRCh38.p7	3:69047462	CTTCATTTATTGGTG[C/T]GGAAGAAACCAAGAT	7110
rs754364352	snp	A/G	1.67111e-05	0.00289055	synonymous-codon	TMF1	GRCh38.p7	3:69025710	GTGATCATGAGACTC[A/G]TCCTATGTTAATTAA	7110
rs754375389	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69045324	TTAGCTGGGCATGGT[A/G]GCAGGCACCTGTAAT	7110
rs754405047	snp	C/T	1.6797e-05	0.00289797	intron-variant	TMF1	GRCh38.p7	3:69038796	TCTTCAACATCCTAC[C/T]CTGATAATTCATTCT	7110
rs754459990	snp	G/T			intron-variant	TMF1	GRCh38.p7	3:69041187	CCCCTCAGTCTCTGA[G/T]ATTGTAAGGCAAGGC	7110
rs754480255	snp	A/G			utr-variant-3-prime	TMF1	GRCh38.p7	3:69022451	TAAATTTTCTCCATT[A/G]TCCAATCACATCTAG	7110
rs754518514	in-del	-/AC			intron-variant	TMF1	GRCh38.p7	3:69023971	TCAAATAAATCACTA[-/AC]ACATACTATAAATTA	7110
rs754532270	snp	C/T	0.000397404	0.0140906	synonymous-codon	TMF1	GRCh38.p7	3:69048234	TTCCCCTGAAACACA[C/T]AAAGAAGAGTCTTTT	7110
rs754534849	snp	A/G	1.6808e-05	0.00289892	missense	TMF1	GRCh38.p7	3:69043808	TTTTCTGCTTCTGCA[A/G]TTCTTTGAGTAAACT	7110
rs754534910	snp	A/T	3.31263e-05	0.00406965	missense	TMF1	GRCh38.p7	3:69035027	TGTGACAGTACCTGC[A/T]GAAGTTCACCGATCT	7110
rs754571898	in-del	-/T			intron-variant	TMF1	GRCh38.p7	3:69030217	CCAAAAGTATTTTAA[-/T]TTCAAAATGGAGTCA	7110
rs754576694	snp	A/T	1.79635e-05	0.0029969	utr-variant-3-prime	TMF1	GRCh38.p7	3:69023151	AATGCTTACATTCAG[A/T]TTGATGGGAATTCAA	7110
rs754584229	snp	C/T	1.65614e-05	0.00287757	synonymous-codon	TMF1	GRCh38.p7	3:69035089	CGCTTGTTCTGTACG[C/T]TGCAATGCAAGCCTA	7110
rs754620726	snp	A/G	3.89401e-05	0.00441231	intron-variant	TMF1	GRCh38.p7	3:69042940	AAATCTGTGAATACC[A/G]TAAAGAATGACTTTC	7110
rs754686283	snp	C/G			intron-variant	TMF1	GRCh38.p7	3:69042668	TCATTCTTCCATAAA[C/G]TGTCACCTATTTCTA	7110
rs754710284	snp	A/G			intron-variant, upstream-variant-2KB	TMF1, MIR3136	GRCh38.p7	3:69049182	TCAAGACAAGCCTGG[A/G]CAACATAGTGAGACC	7110
rs754736536	snp	A/T	1.65831e-05	0.00287945	missense	TMF1	GRCh38.p7	3:69047743	ATTCTTTCAAAAGCA[A/T]CAGATGAACAGCAAC	7110
rs754742270	snp	C/G			intron-variant	TMF1	GRCh38.p7	3:69035508	TATAAACTACCATAG[C/G]CTTTTTGGAAAACGT	7110
rs754743678	in-del	-/AC			intron-variant	TMF1	GRCh38.p7	3:69042312	CCAAGTGCTGAGATT[-/AC]AGTCATAAGCCACCA	7110
rs754753231	snp	C/T	2.05442e-05	0.00320495	intron-variant	TMF1	GRCh38.p7	3:69039058	CAAGAAATAATACCA[C/T]GGTAAATAACTGTAT	7110
rs754758055	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69024917	TTTCCTTTGAGCAGC[A/G]TGTCAGCACTCAAAG	7110
rs754791633	snp	A/G	1.66613e-05	0.00288623	synonymous-codon	TMF1	GRCh38.p7	3:69047843	AAGATGTCTGCATCA[A/G]GTGAAGACTTGATTT	7110
rs754878017	snp	C/T			utr-variant-3-prime	TMF1	GRCh38.p7	3:69022457	TTCTCCATTATCCAA[C/T]CACATCTAGATAACA	7110
rs754884241	snp	A/C	3.31472e-05	0.00407093	intron-variant	TMF1	GRCh38.p7	3:69027894	AACAAAAACAAAATT[A/C]AATACCTTTTCTTTT	7110
rs754905622	snp	C/T	1.65649e-05	0.00287788	missense	TMF1	GRCh38.p7	3:69026064	TTGAGCGTGACATGG[C/T]GGGAGTGCTAGAAAC	7110
rs754937454	snp	A/C			utr-variant-3-prime	TMF1	GRCh38.p7	3:69020008	GATTCACTTTAATGA[A/C]AATGAAAAATTTTGA	7110
rs754943423	in-del	-/A			upstream-variant-2KB	TMF1	GRCh38.p7	3:69054019	TTTATAATAAAACTT[-/A]TTTGTCAATATGTAG	7110
rs754967829	in-del	-/A	1.67125e-05	0.00289067	intron-variant	TMF1	GRCh38.p7	3:69026107	CGTTCCTTAGGGAGT[-/A]AAAAAAAATTCTGTT	7110
rs754977133	snp	A/T			intron-variant	TMF1	GRCh38.p7	3:69026836	GAGTGTTACAAATCA[A/T]AAAATTTCTGGCTTA	7110
rs755071944	snp	A/G	0.000149151	0.00863442	synonymous-codon	TMF1	GRCh38.p7	3:69025614	AGACTGTAGGTTTTC[A/G]ATTATGCTTGATCCT	7110
rs755105455	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69040525	GCAGAAAGATATGGA[A/G]GAGTTGTGGCAAGAT	7110
rs755115899	snp	C/T	3.32613e-05	0.00407793	synonymous-codon	TMF1	GRCh38.p7	3:69024178	TAGATTGCCAATTTC[C/T]AGCTGAGAAGCATTA	7110
rs755125523	in-del	-/A			intron-variant	TMF1	GRCh38.p7	3:69040524	TGCAGAAAGATATGG[-/A]AGAGTTGTGGCAAGA	7110
rs755149328	in-del	-/C	1.85159e-05	0.00304264	intron-variant, downstream-variant-500B	TMF1, MIR3136	GRCh38.p7	3:69048569	AACTTATTCCTTTAA[-/C]AAAAAAGTAAATATT	7110
rs755291100	snp	A/C			utr-variant-5-prime	TMF1	GRCh38.p7	3:69052259	TTACCCTCGGCCGTT[A/C]CCGCACAGCTGAGAC	7110
rs755322077	snp	C/G	8.96419e-05	0.00669424	intron-variant	TMF1	GRCh38.p7	3:69029769	TTAAAAAGTGCTTTA[C/G]GATGTCACGGAACTA	7110
rs755360040	snp	C/T	1.66101e-05	0.0028818	missense	TMF1	GRCh38.p7	3:69038883	GAATACTTCGGTTCT[C/T]TTCTTCAAGTTCATC	7110
rs755377129	snp	A/G	3.3162e-05	0.00407184	synonymous-codon	TMF1	GRCh38.p7	3:69029897	TGTTTTCCTGTCTTA[A/G]AAGAGAATTCTGTGA	7110
rs755377624	snp	A/C	3.35982e-05	0.00409853	intron-variant	TMF1	GRCh38.p7	3:69038803	CATCCTACTCTGATA[A/C]TTCATTCTAAATGGG	7110
rs755477058	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69039450	ATCCTTCTTACATGA[C/T]ATACCCCATTAAATC	7110
rs755528560	in-del	-/AG	3.69734e-05	0.00429945	intron-variant	TMF1	GRCh38.p7	3:69043715	AATCTATATCTCTAT[-/AG]AGTTTAATTAATATT	7110
rs755654207	snp	C/T	1.65938e-05	0.00288039	missense	TMF1	GRCh38.p7	3:69048109	TTCACATCAATTACA[C/T]TTTCAGATACTTTCA	7110
rs755671358	snp	G/T	1.71006e-05	0.00292404	synonymous-codon	TMF1	GRCh38.p7	3:69042907	TTCTTTTATGTTTTT[G/T]ATTTCCTAATAAAAA	7110
rs755728031	snp	C/G	5.46055e-05	0.00522492	intron-variant	TMF1	GRCh38.p7	3:69028345	ATGAAAAAGATGCTA[C/G]TATAGACTATTAAAA	7110
rs755768396	snp	G/T			intron-variant	TMF1	GRCh38.p7	3:69033816	TTTTCCAAGAGAAAA[G/T]AATTTGCTTTTTAAT	7110
rs755833447	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69037907	AAAACAGACAATAAT[A/G]AATCTTGGCAAGGAT	7110
rs755849885	snp	C/G	1.66004e-05	0.00288096	missense	TMF1	GRCh38.p7	3:69052000	CTCCTCTTCCTGGAT[C/G]TCCAGAACCCTGTCA	7110
rs755851674	snp	A/C/G	3.31237e-05	0.00406952	missense	TMF1	GRCh38.p7	3:69035084	GCAGCCGCTTGTTCT[A/C/G]TACGCTGCAATGCAA	7110
rs755861204	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69032276	CACCCCCCCGATTCA[C/T]AAGGAATAGCACAGA	7110
rs755886151	in-del	-/G			intron-variant	TMF1	GRCh38.p7	3:69051653	TGGAAGCTGCGTCGA[-/G]GGGAGAGCTTGAGGG	7110
rs755890716	snp	A/T	3.31329e-05	0.00407005	missense	TMF1	GRCh38.p7	3:69047615	TTTTAGACTTTGGAG[A/T]TGAAGAATTAACTAT	7110
rs755905180	snp	C/T			utr-variant-3-prime	TMF1	GRCh38.p7	3:69021399	CATTCTGCCCTTGAA[C/T]ATTACACACACAAAA	7110
rs755941049	in-del	-/TT	1.93489e-05	0.00311032	intron-variant	TMF1	GRCh38.p7	3:69039038	AAACAGACAAAAGTA[-/TT]TTTCAAGAAATAATA	7110
rs755947477	snp	A/T	1.65638e-05	0.00287778	missense	TMF1	GRCh38.p7	3:69026028	TCTGTAGTCCTGCCA[A/T]ATCAACACCACTTAT	7110
rs755992927	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69037056	TATGCAGATTATACA[A/G]AGAACTCATAATAAC	7110
rs756032574	snp	A/G			intron-variant, upstream-variant-2KB	TMF1, MIR3136	GRCh38.p7	3:69050457	ATGTCTGATTAATTT[A/G]AATACATTCAAAAGA	7110
rs756055938	snp	A/C			intron-variant	TMF1	GRCh38.p7	3:69028499	AAGTGAAAAAGCTCC[A/C]CTTCTGTGCATTTTA	7110
rs756119965	snp	A/G	2.92274e-05	0.00382267	intron-variant, downstream-variant-500B	TMF1, MIR3136	GRCh38.p7	3:69048608	ACACATATATGTTAC[A/G]TTAATATTTCAATCA	7110
rs756205978	snp	C/G	1.65605e-05	0.0028775	missense	TMF1	GRCh38.p7	3:69048392	GAATGGTCTGGACAT[C/G]AGTTGGCGAGAGAAA	7110
rs756210733	snp	C/G			intron-variant	TMF1	GRCh38.p7	3:69025236	AGCTGCTTGAAAGGA[C/G]GAGGGATTCTCTGCT	7110
rs756217117	snp	C/G/T	0.000551194	0.0165922	missense	TMF1	GRCh38.p7	3:69044589	TTTCATTCAGAAATT[C/G/T]AACTGTCTGGATAAG	7110
rs756228728	snp	A/G	1.72374e-05	0.00293571	intron-variant	TMF1	GRCh38.p7	3:69030026	ATTACAGGACAGAAA[A/G]AAAAATCACATACAC	7110
rs756245817	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69028882	GTAGTCTCAAAACTA[C/T]TTTGTGGTGTTATAG	7110
rs756293915	snp	C/T	1.65721e-05	0.0028785	synonymous-codon	TMF1	GRCh38.p7	3:69039617	CTTTGCAACCATATT[C/T]TCATTCTCCTTGTCT	7110
rs756305488	snp	C/T	6.63856e-05	0.00576094	missense	TMF1	GRCh38.p7	3:69024167	CGAGTTTTTTCTAGA[C/T]TGCCAATTTCTAGCT	7110
rs756321147	snp	C/T			utr-variant-3-prime	TMF1	GRCh38.p7	3:69020771	TTTGTAGATAAAGAG[C/T]AATATATGGTAATAT	7110
rs756386533	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69037931	CAAGGATGTGGAGAA[A/G]CTGAAACCCTCACCT	7110
rs756502879	snp	C/T			upstream-variant-2KB	TMF1	GRCh38.p7	3:69053140	TTACAGCAGTCCAAA[C/T]GGACTAAGACACCTA	7110
rs756556496	snp	A/C	1.81181e-05	0.00300977	intron-variant	TMF1	GRCh38.p7	3:69047341	ATCTAAAAATCCCTT[A/C]CACTTACTAGAGTTA	7110
rs756642722	snp	C/G	1.66194e-05	0.00288261	missense	TMF1	GRCh38.p7	3:69025580	AATGAGTGATTTCCC[C/G]TTCCCTTAGCTTTAG	7110
rs756645994	snp	A/T			intron-variant	TMF1	GRCh38.p7	3:69035421	TAAATATTTGCCACA[A/T]CACACAGAAAGTGAT	7110
rs756696411	snp	A/C	1.66763e-05	0.00288753	synonymous-codon	TMF1	GRCh38.p7	3:69047868	TGATTTTGAATCTGT[A/C]GTCTCTTGTCTCGAG	7110
rs756704366	in-del	-/CCT	5.09238e-05	0.00504572	cds-indel	TMF1	GRCh38.p7	3:69052091	AACCAACTCATCGCC[-/CCT]CCTCAGCCGGCAGTG	7110
rs756747423	snp	C/T	1.66349e-05	0.00288395	splice-acceptor-variant	TMF1	GRCh38.p7	3:69039694	TTGAAAGTTTTTCTC[C/T]TGGTGATGGTAAAGA	7110
rs756750761	snp	A/G			utr-variant-3-prime	TMF1	GRCh38.p7	3:69021054	TGGTTTCGGTTACTC[A/G]CGGTCAACCACAGTC	7110
rs756792533	snp	C/G	1.65619e-05	0.00287762	missense	TMF1	GRCh38.p7	3:69038659	TCATTTCACGGCTCA[C/G]AGCAGCTTCCTGTGC	7110
rs756820108	snp	A/G	1.66893e-05	0.00288867	missense	TMF1	GRCh38.p7	3:69047983	ACAGGAGGAGAAGGT[A/G]TATTGCTCTGCCTGT	7110
rs756864910	snp	A/C	1.99519e-05	0.00315841	synonymous-codon	TMF1	GRCh38.p7	3:69027951	CTTCCTTTCTTGTTC[A/C]ACTTTCATTCTTTCC	7110
rs756892716	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69035246	TCCAATGAACTTTTA[C/T]ATATGATTATCACAT	7110
rs757089270	snp	C/T	1.65864e-05	0.00287974	intron-variant	TMF1	GRCh38.p7	3:69034990	AAAAACACATACTTC[C/T]TGGATTTGTGTTTTG	7110
rs757140443	in-del	-/T			intron-variant	TMF1	GRCh38.p7	3:69051036	ATCTTGGGTCACACA[-/T]TTTTCCGGCTAATAC	7110
rs757153451	snp	A/T	2.1365e-05	0.00326834	intron-variant, downstream-variant-500B	TMF1, MIR3136	GRCh38.p7	3:69048585	AAAAAAGTAAATATT[A/T]AAAAAGAACACATAT	7110
rs757177638	snp	A/T	1.80052e-05	0.00300038	missense	TMF1	GRCh38.p7	3:69023296	CATACATCTGCAGAA[A/T]AGTGTTGTACCTTTG	7110
rs757186156	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69046756	CTTAGACATTTCTCT[C/T]TCTCGTTCATGTGAA	7110
rs757277655	snp	A/C			intron-variant	TMF1	GRCh38.p7	3:69028738	GTTAAAAAATACTAA[A/C]CATTGCCTTAATATA	7110
rs757330236	snp	G/T	1.65605e-05	0.0028775	missense	TMF1	GRCh38.p7	3:69048275	CAGTTGTTTCAGGAG[G/T]TCTTGACTGGCCAAT	7110
rs757367062	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69031659	AAAAAAAGAGCAATG[A/G]GTAAGATTCTGAGAT	7110
rs757397317	snp	C/T			intron-variant, upstream-variant-2KB	TMF1, MIR3136	GRCh38.p7	3:69049413	CTCAAACCAAGATAA[C/T]GGTGACAAATGTTCT	7110
rs757406492	snp	A/C	1.87317e-05	0.00306031	intron-variant	TMF1	GRCh38.p7	3:69039023	ACCTATATGTTATAA[A/C]AACAGACAAAAGTAT	7110
rs757442229	snp	C/T	1.6574e-05	0.00287867	synonymous-codon	TMF1	GRCh38.p7	3:69047712	GCTATCTAATGACTG[C/T]ACACTAAATGAGTCT	7110
rs757454617	in-del	-/CTTTT	5.0279e-05	0.00501368	frameshift-variant	TMF1	GRCh38.p7	3:69027900	AACAAAATTCAATAC[-/CTTTT]CTTTTATTGTTTCTT	7110
rs757459410	snp	G/T	1.68704e-05	0.00290429	intron-variant	TMF1	GRCh38.p7	3:69030010	GTCTGGGATTCACCT[G/T]ATTACAGGACAGAAA	7110
rs757496089	snp	A/T	1.65974e-05	0.0028807	missense	TMF1	GRCh38.p7	3:69038923	CTGAAGACGGCCAAG[A/T]TCTTTCTCTTGGCGT	7110
rs757540350	snp	A/C			intron-variant	TMF1	GRCh38.p7	3:69028975	AACATGCCACACAAT[A/C]TCAACAATCTACATG	7110
rs757586099	snp	C/T	1.6617e-05	0.00288239	synonymous-codon	TMF1	GRCh38.p7	3:69044551	ACTAAGAGATAATAA[C/T]TGAGCCTCCCTTTTT	7110
rs757622299	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69042588	TTACAGGGACTTACT[C/T]TTCTTTTTACTTCCA	7110
rs757659109	snp	C/G	1.65762e-05	0.00287886	missense	TMF1	GRCh38.p7	3:69038577	ACTTGAATGGCTAAT[C/G]TTTCTTGCTGCTGAC	7110
rs757709612	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69040811	GCTATAGTCTCAGCT[A/G]TTCGGGAGGCTGAGG	7110
rs757800287	snp	C/G	3.31752e-05	0.00407265	missense	TMF1	GRCh38.p7	3:69024153	CAGCCATTATTGATC[C/G]AGTTTTTTCTAGATT	7110
rs757812984	snp	A/G	1.65605e-05	0.0028775	stop-gained	TMF1	GRCh38.p7	3:69048377	CCACTGGACTCTTCT[A/G]AATGGTCTGGACATC	7110
rs757816843	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69030106	AATGATGCAAGTAGC[C/T]ACACTTAAAACTGAT	7110
rs757898172	snp	A/G			downstream-variant-500B	TMF1	GRCh38.p7	3:69019788	TCTTCACTCATTACT[A/G]TTGACCACTATAAAT	7110
rs757928297	snp	A/T	1.66189e-05	0.00288256	synonymous-codon	TMF1	GRCh38.p7	3:69044542	TTTTTCCTTACTAAG[A/T]GATAATAACTGAGCC	7110
rs757937820	snp	C/T	1.65905e-05	0.0028801	missense	TMF1	GRCh38.p7	3:69047755	GCATCAGATGAACAG[C/T]AACTCTCAGTGAGTT	7110
rs757969054	snp	G/T	3.33289e-05	0.00408207	intron-variant	TMF1	GRCh38.p7	3:69026106	TGCGTTCCTTAGGGA[G/T]TAAAAAAAATTCTGT	7110
rs758012143	snp	A/G			utr-variant-3-prime	TMF1	GRCh38.p7	3:69021184	CTATTTGCAGTTATT[A/G]TTTATCTCTTGCTGT	7110
rs758060628	snp	A/G	1.65666e-05	0.00287802	intron-variant	TMF1	GRCh38.p7	3:69035118	TAAGGTCCCCCACCT[A/G]TAGGAGGAGAAACAA	7110
rs758138758	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69024611	CCCTGTATAGCATAC[C/T]AGCTATACAAACATC	7110
rs758142303	snp	C/G			intron-variant	TMF1	GRCh38.p7	3:69046153	GTAATTTTAGAAAAC[C/G]CATAAGAATTTTTAA	7110
rs758187213	snp	C/T	1.65748e-05	0.00287874	synonymous-codon	TMF1	GRCh38.p7	3:69039632	TTCATTCTCCTTGTC[C/T]TTAGCTCTTAATTTC	7110
rs758242083	snp	A/G	0.000389788	0.013955	intron-variant	TMF1	GRCh38.p7	3:69042625	AAAAGCTAGAAACAC[A/G]TATCTCTGTCTCAAT	7110
rs758277193	snp	C/T	1.66665e-05	0.00288669	missense	TMF1	GRCh38.p7	3:69047851	TGCATCAAGTGAAGA[C/T]TTGATTTTGAATCTG	7110
rs758340340	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69034104	AGGCATGAACCACCA[C/T]GCCCAGCCCTTAATT	7110
rs758371356	snp	A/C	3.54805e-05	0.00421177	intron-variant	TMF1	GRCh38.p7	3:69028181	CCATCCCCAACCATT[A/C]TCTAATGTATGCCCT	7110
rs758372807	in-del	-/CTACT	1.69192e-05	0.00290849	intron-variant	TMF1	GRCh38.p7	3:69038536	CAAATATTTTTAAAA[-/CTACT]CTAATTCATCATCCA	7110
rs758456318	in-del	-/T			upstream-variant-2KB, utr-variant-5-prime	TMF1	GRCh38.p7	3:69052375	AAGAACAGAAGAACG[-/T]TGACGTCACATCCGG	7110
rs758470723	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69051882	CTCTACACCACTTAA[C/T]CTGCCTGCATCAAGA	7110
rs758517291	snp	C/G/T	4.96967e-05	0.00498461	synonymous-codon	TMF1	GRCh38.p7	3:69047610	AACTGTTTTAGACTT[C/G/T]GGAGTTGAAGAATTA	7110
rs758576751	snp	A/C	0.000134841	0.0082099	intron-variant	TMF1	GRCh38.p7	3:69025733	TTAATTAAGAAAGTT[A/C]ACACAGTTACTCAGT	7110
rs758653505	snp	A/C			intron-variant	TMF1	GRCh38.p7	3:69032027	CCTATAAATTTAAAT[A/C]TATATGAAGGTTTAT	7110
rs758674163	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69040410	TCAAGGAAAACGTAC[C/T]TGCCCTTGGGAGATG	7110
rs758700419	snp	A/G	1.66037e-05	0.00288125	missense	TMF1	GRCh38.p7	3:69051983	TCGGCCCAGATGCTC[A/G]GCTCCTCTTCCTGGA	7110
rs758748986	snp	A/G	1.65614e-05	0.00287757	missense	TMF1	GRCh38.p7	3:69047476	GTGGAAGAAACCAAG[A/G]TATCAGGCTGTTCAC	7110
rs758750329	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69030563	GCAAATAAATGCAAA[C/T]CATATATCTAGGATT	7110
rs758755983	snp	A/C			intron-variant	TMF1	GRCh38.p7	3:69031910	AGCATTCATTTATTG[A/C]TAAATATTTATTTCA	7110
rs758762147	snp	A/G	1.65611e-05	0.00287755	missense	TMF1	GRCh38.p7	3:69048241	GAAACACACAAAGAA[A/G]AGTCTTTTACTTGTG	7110
rs758764531	snp	C/T	1.65776e-05	0.00287898	missense	TMF1	GRCh38.p7	3:69029918	AATTCTGTGACTCCA[C/T]GGAAGACATCTGAAT	7110
rs758776241	snp	C/G	1.66272e-05	0.00288328	missense	TMF1	GRCh38.p7	3:69029971	GTAGCTGCACGTTCT[C/G]TCTCAACTGCTGCTG	7110
rs758815357	snp	A/G	1.67638e-05	0.0028951	missense	TMF1	GRCh38.p7	3:69043835	AACTCATCTTTCAAG[A/G]AAGAAATGCTACTGC	7110
rs759021746	snp	C/T	8.27986e-05	0.0064337	missense	TMF1	GRCh38.p7	3:69048446	CATCGACCACAGTCC[C/T]CCGAACTGGCTTTGT	7110
rs759131376	in-del	-/A	1.83068e-05	0.0030254	intron-variant	TMF1	GRCh38.p7	3:69047330	CCAAAAAGCACATCT[-/A]AAAATCCCTTCCACT	7110
rs759147166	snp	A/C			intron-variant	TMF1	GRCh38.p7	3:69026124	AAAAAAATTCTGTTC[A/C]TATTAAAGAGCAAAG	7110
rs759184531	snp	A/C/T	3.33563e-05	0.00408378	intron-variant	TMF1	GRCh38.p7	3:69039537	ATATGTAGAGAATTA[A/C/T]GATTGCTATTCACCT	7110
rs759213331	in-del	-/ATC			intron-variant	TMF1	GRCh38.p7	3:69036181	TGTTTTACTAGAGTG[-/ATC]ATCAGGATATTTTAC	7110
rs759235158	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69024521	CAGAGAAATAAAAAT[A/G]TACTTTAACGTAGCC	7110
rs759334888	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69051321	CCCTACTAAAAATAC[A/G]AAAAGTTGCCGGGCG	7110
rs759444437	snp	C/T	2.27167e-05	0.00337014	intron-variant	TMF1	GRCh38.p7	3:69028020	AATAAAGTTAGACAA[C/T]TTCTGTGATAGTAAT	7110
rs759507589	snp	C/T	1.69853e-05	0.00291416	intron-variant	TMF1	GRCh38.p7	3:69038529	GCATAAACAAATATT[C/T]TTAAAACTACTCTAA	7110
rs759518991	snp	A/G	0.000248911	0.0111532	intron-variant	TMF1	GRCh38.p7	3:69034974	ATTCTTTTATTTCTA[A/G]AAAAACACATACTTC	7110
rs759562627	snp	C/T	1.65638e-05	0.00287778	missense	TMF1	GRCh38.p7	3:69038623	CCTTCTCTAATGCTG[C/T]AGAAAGTTCTTCTTT	7110
rs759574122	snp	A/G	0.000117378	0.00765997	intron-variant	TMF1	GRCh38.p7	3:69025721	ACTCATCCTATGTTA[A/G]TTAAGAAAGTTCACA	7110
rs759595005	snp	C/T	3.6297e-05	0.00425995	intron-variant	TMF1	GRCh38.p7	3:69043740	TAATATTACTTTAAA[C/T]TTCAATTACCTTTTT	7110
rs759652439	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69040352	TGCTGGATTACACTT[C/T]TGAATTAATGCTGAT	7110
rs759684968	snp	A/C	4.9717e-05	0.00498558	synonymous-codon	TMF1	GRCh38.p7	3:69042859	TTTCAAAAGGTCTGC[A/C]GTTTCACTACTATTT	7110
rs759774953	snp	A/C			intron-variant	TMF1	GRCh38.p7	3:69042451	TATCATACAGTACTT[A/C]AGCTAGGTATTCAGA	7110
rs759788017	snp	C/G			missense	TMF1	GRCh38.p7	3:69048384	ACTCTTCTGAATGGT[C/G]TGGACATCAGTTGGC	7110
rs759812377	snp	G/T	1.6571e-05	0.0028784	missense	TMF1	GRCh38.p7	3:69047682	ATCATCTGAATTGAT[G/T]TCACTTACACTCCGG	7110
rs759877321	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69023705	ACATATTCTCACTTA[C/T]GGCTTAACAGTGTCT	7110
rs759944004	snp	A/G			utr-variant-3-prime	TMF1	GRCh38.p7	3:69020861	TTATAAAATTGAAAA[A/G]TTTAGGAATGAGTTT	7110
rs759974051	snp	C/T	8.28096e-05	0.00643412	missense	TMF1	GRCh38.p7	3:69035037	CCTGCTGAAGTTCAC[C/T]GATCTCATGGCGTAA	7110
rs760026516	snp	C/T	1.65641e-05	0.00287781	synonymous-codon	TMF1	GRCh38.p7	3:69047580	TACTTCTTCAGATTT[C/T]CCTTCAGCAGATTCA	7110
rs760038720	snp	C/T	4.97121e-05	0.00498534	synonymous-codon	TMF1	GRCh38.p7	3:69026011	CTGAGACAGAAAAGA[C/T]GTCTGTAGTCCTGCC	7110
rs760077599	snp	C/T			upstream-variant-2KB	TMF1	GRCh38.p7	3:69052472	TACAGCAGTTCTTAG[C/T]GAAGGGGAAGCTATG	7110
rs760099404	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69026414	CCAACTTGACTAACA[C/T]GGAAAAACCTCGTCT	7110
rs760143543	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69036091	CCCAAATATCCATCA[A/G]TAAGAAATAGCTGAA	7110
rs760281565	snp	C/T	0.000116367	0.00762692	missense	TMF1	GRCh38.p7	3:69038876	GCAGCCTGAATACTT[C/T]GGTTCTTTTCTTCAA	7110
rs760284848	snp	C/G	1.65622e-05	0.00287764	missense	TMF1	GRCh38.p7	3:69048202	GTTTTAGGTGATGAA[C/G]TACCTGCTGCCAGAG	7110
rs760317132	snp	A/C			intron-variant	TMF1	GRCh38.p7	3:69047286	TTATGCATCAATGAA[A/C]GTATTTTTTAAAACA	7110
rs760420683	snp	A/C			intron-variant	TMF1	GRCh38.p7	3:69031280	GTAGGTGTGTTTCCA[A/C]AAGGGTAACATTAAG	7110
rs760465095	snp	G/T	0.000101451	0.00712145	missense	TMF1	GRCh38.p7	3:69043793	GCTAGTTGAACTTTC[G/T]TTTCTGCTTCTGCAA	7110
rs760508304	snp	A/G	1.76459e-05	0.00297029	stop-gained	TMF1	GRCh38.p7	3:69023251	CTTCGAGATCTAATC[A/G]AAGTTCTTCTGCCTC	7110
rs760523573	snp	C/T	1.75062e-05	0.00295852	utr-variant-5-prime	TMF1	GRCh38.p7	3:69052137	CAAGCGGGAAGGCCT[C/T]AGGCCTGGGGAAGGG	7110
rs760523896	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69051564	TCCCTGATGATTTAC[A/G]TACTTCAGACCTTGG	7110
rs760562252	snp	A/T	6.64341e-05	0.00576304	intron-variant	TMF1	GRCh38.p7	3:69035162	AATGGTACAGTATTA[A/T]CTATAACTTCCCACT	7110
rs760624159	snp	C/T	1.65603e-05	0.00287747	missense	TMF1	GRCh38.p7	3:69048317	CATGTAAGCTGCTTT[C/T]CACTTCTTCTTCTGG	7110
rs760625235	in-del	-/TGT	1.65616e-05	0.00287759	cds-indel	TMF1	GRCh38.p7	3:69047484	ACCAAGATATCAGGC[-/TGT]TGTTCACAGTTAACA	7110
rs760699523	snp	C/G/T	1.66651e-05	0.00288657	missense	TMF1	GRCh38.p7	3:69038946	CTTGGCGTTCTACCA[C/G/T]GGAATTTAGTTTTTT	7110
rs760709514	snp	C/T	1.65638e-05	0.00287778	missense	TMF1	GRCh38.p7	3:69033624	TGCTTGCAAATTTTC[C/T]ATTTGTCGAAGCAAT	7110
rs760758303	snp	A/G	1.67984e-05	0.00289809	synonymous-codon	TMF1	GRCh38.p7	3:69028265	TGTTCTTACATATTC[A/G]TCTTTTAGGTTTTCC	7110
rs760779731	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69043549	TGGGCTCAAGTGATC[C/T]GCCCACTTCAGCCTC	7110
rs760795221	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69042183	CTGGGATTAGAGGCA[C/T]GCACCACCACCACCC	7110
rs760802883	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69042546	CTGTTTAAAGTTTTC[C/T]TAGGGCAGCACAAAT	7110
rs760823105	snp	A/G	3.34074e-05	0.00408688	synonymous-codon	TMF1	GRCh38.p7	3:69047921	CACTTTCATGATCTA[A/G]AACTTCAATATCACT	7110
rs760851579	snp	A/C	1.65803e-05	0.00287922	splice-donor-variant	TMF1	GRCh38.p7	3:69042805	CCAAATACTATACGC[A/C]CCTTCTTCCATTAAC	7110
rs760909405	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69031451	ATACACAAATGAGTA[C/T]CAATAAAACTTTGGA	7110
rs760915655	snp	C/T	1.66635e-05	0.00288643	missense	TMF1	GRCh38.p7	3:69051954	TCTTACCCGGCTCTC[C/T]ATACGGAATGGTCTC	7110
rs760946338	snp	A/C			intron-variant	TMF1	GRCh38.p7	3:69037379	GCATGGTGGCTCATG[A/C]CTGTAATCCAAGCAC	7110
rs760996031	snp	A/C/G	6.62541e-05	0.00575528	synonymous-codon	TMF1	GRCh38.p7	3:69047574	TTCATTTACTTCTTC[A/C/G]GATTTTCCTTCAGCA	7110
rs761008192	in-del	-/TATGAAA			intron-variant	TMF1	GRCh38.p7	3:69035829	ACGTAAGACATCAAT[-/TATGAAA]AACACATATATGGGA	7110
rs761142779	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69040664	GGGTGCAGTGGCTCA[C/T]GCCTGTAATCCCAGC	7110
rs761196054	snp	A/G	1.67307e-05	0.00289224	intron-variant	TMF1	GRCh38.p7	3:69033735	CTGAAGTCATTACCA[A/G]TGACAGCAATAAAAA	7110
rs761232643	in-del	-/TAA			intron-variant	TMF1	GRCh38.p7	3:69026817	GTAACATAAAATTAC[-/TAA]TGAGTGTTACAAATC	7110
rs761268611	snp	C/T	6.66278e-05	0.00577143	missense	TMF1	GRCh38.p7	3:69025700	GTCCAAATGAGTGAT[C/T]ATGAGACTCATCCTA	7110
rs761270002	snp	C/T			missense	TMF1	GRCh38.p7	3:69024086	AGTTTGGGTATCTCC[C/T]TCACCTTCTCTTCAA	7110
rs761271958	snp	C/G	1.67281e-05	0.00289202	missense	TMF1	GRCh38.p7	3:69038852	TCTTACTTGTATGCA[C/G]TATCCAGGGCAGCCT	7110
rs761301391	snp	A/C	1.65644e-05	0.00287783	missense	TMF1	GRCh38.p7	3:69047555	CAGTGGGTATAACTA[A/C]TGTTTCATTTACTTC	7110
rs761358152	snp	C/T			upstream-variant-2KB	TMF1	GRCh38.p7	3:69053380	ATTTCCAGCTGCTTT[C/T]GAAAAATATGAATAC	7110
rs761371561	snp	C/G	6.66267e-05	0.00577139	intron-variant	TMF1	GRCh38.p7	3:69038761	AATGTTGCCAGTGAT[C/G]AGATAATAGAAAAAG	7110
rs761387578	snp	C/T	4.97963e-05	0.00498955	missense	TMF1	GRCh38.p7	3:69047426	CACACTGCTCAGCCA[C/T]CTTGTCTAACACAGT	7110
rs761481712	snp	C/T	2.07699e-05	0.00322251	intron-variant, downstream-variant-500B	TMF1, MIR3136	GRCh38.p7	3:69048583	ACAAAAAAGTAAATA[C/T]TAAAAAAGAACACAT	7110
rs761489266	in-del	-/AA	1.72946e-05	0.00294058	intron-variant	TMF1	GRCh38.p7	3:69025540	ATTTACTTCTATAGC[-/AA]ATTTAATTTTTCCAA	7110
rs761508354	snp	A/T	3.32651e-05	0.00407817	synonymous-codon	TMF1	GRCh38.p7	3:69025692	AGGCATTGGTCCAAA[A/T]GAGTGATCATGAGAC	7110
rs761568235	snp	C/G			upstream-variant-2KB	TMF1	GRCh38.p7	3:69052528	GGAAGGAATATTCAA[C/G]TTTTCGTGTGTGTGC	7110
rs761572784	snp	C/T			intron-variant, upstream-variant-2KB	TMF1, MIR3136	GRCh38.p7	3:69049843	AAAATGTTTTCTTTT[C/T]CAAATTAAAATGTGG	7110
rs761595179	snp	C/G	1.66018e-05	0.00288108	missense	TMF1	GRCh38.p7	3:69048091	ATACTTTCCATAGTT[C/G]TTTTCACATCAATTA	7110
rs761609297	snp	C/T	9.97407e-05	0.00706119	synonymous-codon	TMF1	GRCh38.p7	3:69029865	TTTCTCTGATTCTAG[C/T]TGGGCTTGAAATCTA	7110
rs761663727	snp	A/G	1.65649e-05	0.00287788	missense	TMF1	GRCh38.p7	3:69048187	TCGTGCTTGCCTTCA[A/G]TTTTAGGTGATGAAG	7110
rs761671303	snp	A/C			intron-variant	TMF1	GRCh38.p7	3:69040363	ACTTCTGAATTAATG[A/C]TGATTTCTTAGGTTT	7110
rs761715035	snp	C/T	1.76232e-05	0.00296838	missense	TMF1	GRCh38.p7	3:69043755	TTTCAATTACCTTTT[C/T]AGCAGCATCTCTCTC	7110
rs761752378	snp	A/C			intron-variant, upstream-variant-2KB	TMF1, MIR3136	GRCh38.p7	3:69049077	TAGTTATGAGCTAGA[A/C]AAAGGGCAACACTCA	7110
rs761753339	snp	G/T			intron-variant	TMF1	GRCh38.p7	3:69034424	GGTGCAGTGAGCCAA[G/T]ATTGTGCCACTGCAC	7110
rs761867425	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69040996	AAATGTAAATACTCT[A/G]TGAATATAAAATACT	7110
rs761946532	snp	G/T	2.17621e-05	0.00329857	intron-variant	TMF1	GRCh38.p7	3:69028003	AATGTCTAATAGAGA[G/T]AAATAAAGTTAGACA	7110
rs761960395	snp	C/G			missense	TMF1	GRCh38.p7	3:69038719	GAAGATCAGTAAGTT[C/G]TCTTAAAAAATTAGA	7110
rs762003130	snp	C/T	1.67013e-05	0.0028897	missense	TMF1	GRCh38.p7	3:69047903	CTGAGCTCTCACTTA[C/T]TACACTTTCATGATC	7110
rs762067257	snp	G/T			missense	TMF1	GRCh38.p7	3:69024175	TTCTAGATTGCCAAT[G/T]TCTAGCTGAGAAGCA	7110
rs762179253	snp	C/T	1.67984e-05	0.00289809	synonymous-codon, downstream-variant-500B	TMF1, MIR3136	GRCh38.p7	3:69048540	TGAAGTATCCCATCC[C/T]CCACTGACAGGGGAA	7110
rs762188496	in-del	-/C			intron-variant	TMF1	GRCh38.p7	3:69042802	CAACCAAATACTATA[-/C]GCACCTTCTTCCATT	7110
rs762203584	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69045953	CCCAGCTACTAGAGC[A/G]GATTAGGTGGGAGGA	7110
rs762261436	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69043678	TTTCCAATATCAAAA[C/T]ACGATGAATGCACTC	7110
rs762339314	snp	A/G	1.66197e-05	0.00288263	intron-variant	TMF1	GRCh38.p7	3:69033712	TGGAGTCTCTGAATC[A/G]TGAAATTCTGAAGTC	7110
rs762372045	snp	A/C	6.38835e-05	0.00565134	intron-variant	TMF1	GRCh38.p7	3:69042555	GTTTTCTTAGGGCAG[A/C]ACAAATTTCTGTCTA	7110
rs762420849	in-del	-/TTA	3.44768e-05	0.00415177	intron-variant	TMF1	GRCh38.p7	3:69025949	ATTTGCATATTTCCT[-/TTA]TTATTATTCTAAGAA	7110
rs762422064	snp	C/G	1.66374e-05	0.00288417	synonymous-codon, downstream-variant-500B	TMF1, MIR3136	GRCh38.p7	3:69048522	TGATTTCAACCCCCA[C/G]GTTGAAGTATCCCAT	7110
rs762422390	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69036522	CAGAACATGTAAGTA[C/T]ATAGATACATATATT	7110
rs762461508	snp	C/G	1.66214e-05	0.00288278	missense	TMF1	GRCh38.p7	3:69024105	CCTTCTCTTCAAGTT[C/G]ATCATTTTGATTTGT	7110
rs762546989	snp	A/G	4.96816e-05	0.00498381	missense	TMF1	GRCh38.p7	3:69048449	CGACCACAGTCCTCC[A/G]AACTGGCTTTGTGAT	7110
rs762604760	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69030380	ATGTAAAACATGAAA[C/T]TATAAAACTTTTAGG	7110
rs762668838	snp	C/T	3.50067e-05	0.00418355	intron-variant	TMF1	GRCh38.p7	3:69025516	CTATTTATTAGGCCT[C/T]AAAACTTCATTTACT	7110
rs762699696	in-del	-/A	0.00026908	0.011596	intron-variant	TMF1	GRCh38.p7	3:69030023	CTGATTACAGGACAG[-/A]AAAAAAAATCACATA	7110
rs762722565	snp	C/T			upstream-variant-2KB	TMF1	GRCh38.p7	3:69053760	GATTTGGGGCAGATT[C/T]GGGTTGAAATTAGCT	7110
rs762736143	snp	A/T	1.6701e-05	0.00288968	missense	TMF1	GRCh38.p7	3:69047964	ACCTGATGAAAAGGT[A/T]CTAACAGGAGGAGAA	7110
rs762756295	snp	A/T	8.30792e-05	0.00644459	synonymous-codon	TMF1	GRCh38.p7	3:69048075	CGTAGACGTATTAGA[A/T]ATACTTTCCATAGTT	7110
rs762759417	snp	G/T	1.66261e-05	0.00288319	intron-variant	TMF1	GRCh38.p7	3:69038751	TGAGTTTATAAATGT[G/T]GCCAGTGATCAGATA	7110
rs762801975	snp	C/G			intron-variant	TMF1	GRCh38.p7	3:69042337	GCCACCACACTCAGC[C/G]AACCCTGTTTATTTT	7110
rs762903721	snp	C/G	1.70235e-05	0.00291744	missense	TMF1	GRCh38.p7	3:69029834	TGTTCTCATCCTCCA[C/G]TTTACACAGCCTATT	7110
rs762939997	snp	A/G	5.1553e-05	0.0050768	utr-variant-5-prime	TMF1	GRCh38.p7	3:69052111	TCAGCCGGCAGTGGC[A/G]GCGGCAGCACCAAGC	7110
rs762994883	snp	A/T	3.3699e-05	0.00410467	synonymous-codon	TMF1	GRCh38.p7	3:69028286	TAGGTTTTCCAATTC[A/T]ACCTGGTACCTATTA	7110
rs763024191	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69041307	TTATCTGTGTTCCTA[C/T]ATTTCCCTCTCACTG	7110
rs763044568	snp	C/T	3.49375e-05	0.00417942	intron-variant	TMF1	GRCh38.p7	3:69043919	AGGATGGTGTCTATA[C/T]ATCCCAAAGGTATAC	7110
rs763070190	snp	C/G			upstream-variant-2KB	TMF1	GRCh38.p7	3:69052881	CCTAATCTCCAATGG[C/G]ACAGTATTAAGGGGA	7110
rs763081282	in-del	-/ATTAT	1.66157e-05	0.00288229	frameshift-variant	TMF1	GRCh38.p7	3:69047790	GAAATCATCTAAACG[-/ATTAT]ATTCAGGACAAGCAG	7110
rs763090326	snp	A/G	6.30895e-05	0.00561612	intron-variant	TMF1	GRCh38.p7	3:69027859	ATCACAGCATCTACT[A/G]AATGGTTACACCACA	7110
rs763093192	snp	A/T			intron-variant	TMF1	GRCh38.p7	3:69027424	ATTAAATTCATTTTT[A/T]AAAAGGGCAAGAGGT	7110
rs763119083	snp	C/G	1.65611e-05	0.00287755	missense	TMF1	GRCh38.p7	3:69035072	TCCTCCTTTCTGGCA[C/G]CCGCTTGTTCTGTAC	7110
rs763144368	snp	A/G/T	9.94356e-05	0.00705046	synonymous-codon, missense	TMF1	GRCh38.p7	3:69047696	TTTCACTTACACTCC[A/G/T]GCTATCTAATGACTG	7110
rs763172290	snp	C/T	0.000116249	0.00762306	synonymous-codon	TMF1	GRCh38.p7	3:69026020	AAAAGATGTCTGTAG[C/T]CCTGCCATATCAACA	7110
rs763218958	in-del	-/A			intron-variant	TMF1	GRCh38.p7	3:69033275	TGAGACTCCATCTCA[-/A]AAAAAAAAAAAAAAA	7110
rs763267651	snp	A/T			intron-variant, upstream-variant-2KB	TMF1, MIR3136	GRCh38.p7	3:69049078	AGTTATGAGCTAGAC[A/T]AAGGGCAACACTCAA	7110
rs763395299	snp	G/T	1.66463e-05	0.00288494	intron-variant	TMF1	GRCh38.p7	3:69039542	TAGAGAATTATGATT[G/T]CTATTCACCTGTTTC	7110
rs763459868	snp	A/G	1.65625e-05	0.00287766	synonymous-codon	TMF1	GRCh38.p7	3:69038654	AGCTTTCATTTCACG[A/G]CTCAGAGCAGCTTCC	7110
rs763460465	snp	C/G			intron-variant	TMF1	GRCh38.p7	3:69045960	ACTAGAGCGGATTAG[C/G]TGGGAGGACTGCTTG	7110
rs763483475	snp	C/G	1.80007e-05	0.003	missense	TMF1	GRCh38.p7	3:69039009	CTTTGCCATCAAGGA[C/G]CTATATGTTATAAAA	7110
rs763485480	snp	C/G	1.66302e-05	0.00288355	missense	TMF1	GRCh38.p7	3:69047803	CGATTATATTCAGGA[C/G]AAGCAGATGCAGAGA	7110
rs763573473	snp	A/C			intron-variant	TMF1	GRCh38.p7	3:69033716	GTCTCTGAATCATGA[A/C]ATTCTGAAGTCATTA	7110
rs763633166	in-del	-/T			intron-variant, upstream-variant-2KB	TMF1, MIR3136	GRCh38.p7	3:69049461	AACTGATGGGAATGG[-/T]TAAGTTCTAGAGAAC	7110
rs763657861	snp	C/T			intron-variant, upstream-variant-2KB	TMF1, MIR3136	GRCh38.p7	3:69049480	GTTCTAGAGAACAAA[C/T]TCATTTTCATCCACT	7110
rs763664049	snp	G/T	1.66369e-05	0.00288412	intron-variant	TMF1	GRCh38.p7	3:69038756	TTATAAATGTTGCCA[G/T]TGATCAGATAATAGA	7110
rs763690307	snp	C/T	3.71223e-05	0.0043081	intron-variant	TMF1	GRCh38.p7	3:69047307	TTTTAAAACAAATGA[C/T]TTAATCTCCAAAAAG	7110
rs763700687	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69026426	ACATGGAAAAACCTC[A/G]TCTCTACTAAAAATA	7110
rs763701576	snp	G/T	1.74998e-05	0.00295797	intron-variant	TMF1	GRCh38.p7	3:69028204	TATGCCCTAAGAGCT[G/T]AGTGGTCACGAAGAG	7110
rs763706208	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69046209	CTAAACAAAAAGTAA[C/T]GCTTGGAATGTCTAA	7110
rs763717440	snp	C/T	1.65608e-05	0.00287752	missense, downstream-variant-500B	TMF1, MIR3136	GRCh38.p7	3:69048464	GAACTGGCTTTGTGA[C/T]TGCTTTAGGAGAGGC	7110
rs763753553	snp	A/G	3.32281e-05	0.0040759	synonymous-codon	TMF1	GRCh38.p7	3:69048078	AGACGTATTAGATAT[A/G]CTTTCCATAGTTGTT	7110
rs763786709	snp	A/T	3.32358e-05	0.00407637	missense	TMF1	GRCh38.p7	3:69044545	TTCCTTACTAAGAGA[A/T]AATAACTGAGCCTCC	7110
rs763786864	snp	A/C			intron-variant	TMF1	GRCh38.p7	3:69033871	GGTCCCGCTCTGTCA[A/C]CCAGGCTGGAGTGCA	7110
rs763817591	in-del	-/TTGGAG	1.65658e-05	0.00287795	cds-indel	TMF1	GRCh38.p7	3:69047609	CAACTGTTTTAGACT[-/TTGGAG]TTGAAGAATTAACTA	7110
rs763834203	snp	A/G	0.000124432	0.00788674	intron-variant	TMF1	GRCh38.p7	3:69042633	GAAACACGTATCTCT[A/G]TCTCAATATATCTTA	7110
rs763844614	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69034145	CTGTTCAATCCTTCC[A/G]AGAGAGTTAGATTGT	7110
rs763915078	snp	C/T			missense	TMF1	GRCh38.p7	3:69038988	TATGTTGTTTCTCAA[C/T]CTCTTCTTTGCCATC	7110
rs763925831	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69024918	TTCCTTTGAGCAGCA[C/T]GTCAGCACTCAAAGT	7110
rs764002680	snp	C/G			intron-variant	TMF1	GRCh38.p7	3:69051656	GAAGCTGCGTCGAGG[C/G]AGAGCTTGAGGGCAA	7110
rs764115187	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69040261	TGCAATGGGCAAACT[C/T]TGGATCCTGGGGCAG	7110
rs764131276	snp	C/G/T	0.000124283	0.00788214	intron-variant	TMF1	GRCh38.p7	3:69027870	TACTAAATGGTTACA[C/G/T]CACAAACAAACAAAA	7110
rs764136402	snp	A/T	1.6696e-05	0.00288924	synonymous-codon	TMF1	GRCh38.p7	3:69047973	AAAGGTACTAACAGG[A/T]GGAGAAGGTGTATTG	7110
rs764180739	snp	A/C	1.6912e-05	0.00290787	missense	TMF1	GRCh38.p7	3:69028295	CAATTCAACCTGGTA[A/C]CTATTAAACAAGGCA	7110
rs764194103	snp	C/T	1.66001e-05	0.00288094	synonymous-codon	TMF1	GRCh38.p7	3:69051988	CCAGATGCTCGGCTC[C/T]TCTTCCTGGATGTCC	7110
rs764208524	snp	A/T	1.72809e-05	0.00293941	intron-variant	TMF1	GRCh38.p7	3:69030028	TACAGGACAGAAAAA[A/T]AAATCACATACACAT	7110
rs764282646	snp	A/G	1.66313e-05	0.00288364	missense	TMF1	GRCh38.p7	3:69047806	TTATATTCAGGACAA[A/G]CAGATGCAGAGAGAA	7110
rs764282741	snp	C/T	1.81711e-05	0.00301417	intron-variant	TMF1	GRCh38.p7	3:69039013	GCCATCAAGGACCTA[C/T]ATGTTATAAAAACAG	7110
rs764310001	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69042398	ATTTAAAAATTAATA[C/T]AATGAAAAATTCACT	7110
rs764363343	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69040695	ACTTTTGGGAAGCAG[A/G]CGGATCACCAGAGGT	7110
rs764372262	snp	A/G	4.968e-05	0.00498373	missense	TMF1	GRCh38.p7	3:69048349	CGTTGTGATTTTGCT[A/G]GAGGTTTTGATACCA	7110
rs764407500	snp	C/T			intron-variant, upstream-variant-2KB	TMF1, MIR3136	GRCh38.p7	3:69050494	GAATTAATTTTGCCT[C/T]TTGGAGAATACTTTA	7110
rs764436684	snp	A/G	3.47856e-05	0.00417032	utr-variant-5-prime	TMF1	GRCh38.p7	3:69052129	GGCAGCACCAAGCGG[A/G]AAGGCCTCAGGCCTG	7110
rs764473344	snp	C/T			utr-variant-3-prime	TMF1	GRCh38.p7	3:69022144	AAGCTATTCTATGCT[C/T]TCCTTGTGTTTGAAA	7110
rs764494069	snp	A/G	1.71481e-05	0.0029281	intron-variant	TMF1	GRCh38.p7	3:69033510	TATAAACAAGATGGA[A/G]GAGCTTCTGCATCGA	7110
rs764547047	snp	A/T	1.65952e-05	0.00288051	missense	TMF1	GRCh38.p7	3:69024125	TTTTGATTTGTTAAT[A/T]TAACTAGTTCTTCAG	7110
rs764658306	snp	A/T			intron-variant, downstream-variant-500B	TMF1, MIR3136	GRCh38.p7	3:69048617	TGTTACATTAATATT[A/T]CAATCATCATTATAA	7110
rs764747722	snp	A/C			synonymous-codon	TMF1	GRCh38.p7	3:69047496	AGGCTGTTCACAGTT[A/C]ACAGGAGTTGCACTT	7110
rs764793888	snp	G/T	1.66518e-05	0.00288542	synonymous-codon	TMF1	GRCh38.p7	3:69044524	AGCTTCTTCTAGAAG[G/T]GCTTTTTCCTTACTA	7110
rs764841393	snp	G/T	1.65605e-05	0.0028775	missense	TMF1	GRCh38.p7	3:69048331	TTCACTTCTTCTTCT[G/T]GTCGTTGTGATTTTG	7110
rs764845155	snp	C/T	1.67829e-05	0.00289675	intron-variant	TMF1	GRCh38.p7	3:69038542	TTTTTAAAACTACTC[C/T]AATTCATCATCCATT	7110
rs764926509	in-del	-/C			intron-variant	TMF1	GRCh38.p7	3:69045847	GGAAGACCGCTTGAG[-/C]CCAGGAGTTCAAGAC	7110
rs764958080	snp	C/T	1.65718e-05	0.00287848	missense	TMF1	GRCh38.p7	3:69039618	TTTGCAACCATATTT[C/T]CATTCTCCTTGTCTT	7110
rs764980189	snp	A/G	1.66643e-05	0.0028865	synonymous-codon	TMF1	GRCh38.p7	3:69047844	AGATGTCTGCATCAA[A/G]TGAAGACTTGATTTT	7110
rs765030966	snp	C/T			upstream-variant-2KB	TMF1	GRCh38.p7	3:69053517	ATTTACCTTATATGC[C/T]TGCCTCCCATATTTG	7110
rs765049560	in-del	-/CA	1.68335e-05	0.00290111	intron-variant	TMF1	GRCh38.p7	3:69025733	TTAATTAAGAAAGTT[-/CA]CACAGTTACTCAGTT	7110
rs765237044	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69025845	AAAATCATTCACGTG[C/T]TTCCTCTCACTAAAA	7110
rs765260812	snp	A/C	1.65699e-05	0.00287831	missense	TMF1	GRCh38.p7	3:69026014	AGACAGAAAAGATGT[A/C]TGTAGTCCTGCCATA	7110
rs765274562	snp	C/T	3.31219e-05	0.00406938	synonymous-codon	TMF1	GRCh38.p7	3:69035059	ATGGCGTAAATAATC[C/T]TCCTTTCTGGCAGCC	7110
rs765329453	snp	A/G	3.31274e-05	0.00406972	synonymous-codon	TMF1	GRCh38.p7	3:69038627	CTCTAATGCTGCAGA[A/G]AGTTCTTCTTTAGCT	7110
rs765335168	snp	C/T	3.35604e-05	0.00409623	intron-variant	TMF1	GRCh38.p7	3:69025723	TCATCCTATGTTAAT[C/T]AAGAAAGTTCACACA	7110
rs765337517	snp	A/C/G	3.32095e-05	0.00407478	synonymous-codon	TMF1	GRCh38.p7	3:69051982	CTCGGCCCAGATGCT[A/C/G]GGCTCCTCTTCCTGG	7110
rs765424845	snp	G/T	1.65649e-05	0.00287788	missense	TMF1	GRCh38.p7	3:69047584	TCTTCAGATTTTCCT[G/T]CAGCAGATTCAACTG	7110
rs765488401	snp	C/T			upstream-variant-2KB	TMF1	GRCh38.p7	3:69052547	TCGTGTGTGTGCTTT[C/T]CAGGAAAATAGTTCA	7110
rs765510025	snp	A/T	1.65941e-05	0.00288041	intron-variant	TMF1	GRCh38.p7	3:69034977	CTTTTATTTCTAGAA[A/T]AACACATACTTCTTG	7110
rs765545925	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69042642	ATCTCTGTCTCAATA[C/T]ATCTTATTCCTCATT	7110
rs765554859	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69039150	TGCCCAGGGTGGAAT[A/G]TTCTGGCTCACTGCA	7110
rs765579675	in-del	-/ACC			intron-variant	TMF1	GRCh38.p7	3:69045956	GCTACTAGAGCGGAT[-/ACC]TAGGTGGGAGGACTG	7110
rs765584572	snp	A/G	1.76561e-05	0.00297115	synonymous-codon	TMF1	GRCh38.p7	3:69039001	AACCTCTTCTTTGCC[A/G]TCAAGGACCTATATG	7110
rs765609080	snp	G/T			intron-variant, downstream-variant-500B	TMF1, MIR3136	GRCh38.p7	3:69048577	CCTTTAACAAAAAAG[G/T]AAATATTAAAAAAGA	7110
rs765635285	snp	A/T			intron-variant	TMF1	GRCh38.p7	3:69043701	ATGCACTCCTCAAAA[A/T]TCTATATCTCTATAG	7110
rs765761104	in-del	-/GGAAA	1.65611e-05	0.00287755	frameshift-variant	TMF1	GRCh38.p7	3:69035066	AATAATCCTCCTTTC[-/GGAAA]TGGCAGCCGCTTGTT	7110
rs765764540	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69031780	TAGCTATGGTCTTTT[C/T]AATAGCATTCCTTGG	7110
rs765831200	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69037668	AAAATTAGCCAGGCA[C/T]GGTAGCACCTGCCTG	7110
rs765833089	snp	C/T			utr-variant-3-prime	TMF1	GRCh38.p7	3:69021237	TATCATAGGTATATA[C/T]GTATAGGAAAAAACA	7110
rs765847250	snp	A/G	1.65836e-05	0.0028795	synonymous-codon	TMF1	GRCh38.p7	3:69029946	AATTTTGTTAGCAAG[A/G]AGTTCTTCTGTAGCT	7110
rs765880426	snp	C/T	1.65712e-05	0.00287843	missense	TMF1	GRCh38.p7	3:69047690	AATTGATTTCACTTA[C/T]ACTCCGGCTATCTAA	7110
rs765919575	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69036686	TGGAATCATGTAAAT[A/G]TTTTACACATACAAA	7110
rs765949482	snp	A/G	3.31219e-05	0.00406938	missense	TMF1	GRCh38.p7	3:69048226	GCCAGAGTTTCCCCT[A/G]AAACACACAAAGAAG	7110
rs765967390	snp	A/G			intron-variant, upstream-variant-2KB	TMF1, MIR3136	GRCh38.p7	3:69050157	CCCAGCTACTCGGGA[A/G]GTTGAGGCACGAGAA	7110
rs766002872	snp	C/T	1.65603e-05	0.00287747	synonymous-codon	TMF1	GRCh38.p7	3:69048324	GCTGCTTTTCACTTC[C/T]TCTTCTGGTCGTTGT	7110
rs766029989	snp	A/G			utr-variant-3-prime	TMF1	GRCh38.p7	3:69022292	GTGCTAAAAATATGG[A/G]TTTACAAAATATGAA	7110
rs766069846	snp	C/G	0.000239337	0.0109367	intron-variant	TMF1	GRCh38.p7	3:69038515	TTTAATTTGTAGAAG[C/G]ATAAACAAATATTTT	7110
rs766155275	in-del	-/G	0.000374891	0.0136859	intron-variant	TMF1	GRCh38.p7	3:69028011	ATAGAGAGAAATAAA[-/G]TTAGACAATTTCTGT	7110
rs766232535	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69028441	TGATTTTCCAACAGT[A/G]TGTTCCAGATCCCAT	7110
rs766298701	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69040452	ATTTAGGAGCAGAAT[A/G]TTACGGTATTTGTAA	7110
rs766310094	in-del	-/CACATATT	1.71164e-05	0.00292539	intron-variant	TMF1	GRCh38.p7	3:69025964	TATTATTATTCTAAG[-/CACATATT]AACTAAGCACATATA	7110
rs766349936	snp	C/T	3.31389e-05	0.00407042	missense	TMF1	GRCh38.p7	3:69042846	GCTCATCTTTCTCTT[C/T]CAAAAGGTCTGCAGT	7110
rs766461388	snp	C/T	3.31279e-05	0.00406975	synonymous-codon	TMF1	GRCh38.p7	3:69033627	TTGCAAATTTTCTAT[C/T]TGTCGAAGCAATGGT	7110
rs766472914	snp	A/G			upstream-variant-2KB	TMF1	GRCh38.p7	3:69052927	TTAGATGATGATGGA[A/G]CCCTCATAAATGGGG	7110
rs766492330	snp	C/G	1.70734e-05	0.00292172	splice-donor-variant	TMF1	GRCh38.p7	3:69044491	TTTGCAGAATACTTA[C/G]TCTTTCAGGTTATCA	7110
rs766598547	snp	C/T	3.31576e-05	0.00407157	synonymous-codon	TMF1	GRCh38.p7	3:69025602	TAGCTTTAGCTGAGA[C/T]TGTAGGTTTTCAATT	7110
rs766681747	in-del	-/AAG	3.31225e-05	0.00406941	cds-indel	TMF1	GRCh38.p7	3:69048236	CCCCTGAAACACACA[-/AAG]AAGAGTCTTTTACTT	7110
rs766694324	snp	C/T	0.000156335	0.00883987	intron-variant	TMF1	GRCh38.p7	3:69042591	CAGGGACTTACTTTT[C/T]TTTTTACTTCCAAAA	7110
rs766738297	snp	A/G	1.66203e-05	0.00288268	stop-gained	TMF1	GRCh38.p7	3:69038877	CAGCCTGAATACTTC[A/G]GTTCTTTTCTTCAAG	7110
rs766771583	snp	G/T	1.76733e-05	0.0029726	missense, downstream-variant-500B	TMF1, MIR3136	GRCh38.p7	3:69048560	TGACAGGGGAACTTA[G/T]TCCTTTAACAAAAAA	7110
rs766821430	snp	C/T			intron-variant, upstream-variant-2KB	TMF1, MIR3136	GRCh38.p7	3:69049160	AGAGTCATTTGAGTC[C/T]AGGAGTTCAAGACAA	7110
rs766917575	snp	C/T	1.78854e-05	0.00299038	intron-variant	TMF1	GRCh38.p7	3:69028340	AGAAAATGAAAAAGA[C/T]GCTAGTATAGACTAT	7110
rs766974296	snp	A/T	1.66535e-05	0.00288556	missense	TMF1	GRCh38.p7	3:69051956	TTACCCGGCTCTCCA[A/T]ACGGAATGGTCTCGG	7110
rs766993601	snp	C/T	1.67083e-05	0.00289031	synonymous-codon	TMF1	GRCh38.p7	3:69038857	CTTGTATGCACTATC[C/T]AGGGCAGCCTGAATA	7110
rs766997695	in-del	-/AC			intron-variant	TMF1	GRCh38.p7	3:69044213	CTGTGTTATTGATTA[-/AC]ACAGTTTTCTTCAAA	7110
rs767017523	in-del	-/A			intron-variant	TMF1	GRCh38.p7	3:69031061	ATAACACTCAGCAAT[-/A]AAAAAGACTAAACTA	7110
rs767053061	snp	C/G			utr-variant-3-prime	TMF1	GRCh38.p7	3:69022564	TGAAATAAATTTTCA[C/G]ATCAAAATTTTTTTT	7110
rs767094815	snp	C/G			missense	TMF1	GRCh38.p7	3:69038716	TGTGAAGATCAGTAA[C/G]TTCTCTTAAAAAATT	7110
rs767152636	snp	A/G			intron-variant, upstream-variant-2KB	TMF1, MIR3136	GRCh38.p7	3:69050386	TACACATTCATTTGC[A/G]CAATATCCAAACCAG	7110
rs767166844	snp	G/T	1.71493e-05	0.0029282	stop-gained	TMF1	GRCh38.p7	3:69043774	AGCATCTCTCTCTTT[G/T]CAGGCTAGTTGAACT	7110
rs767226623	snp	C/T	1.66599e-05	0.00288611	intron-variant	TMF1	GRCh38.p7	3:69038765	TTGCCAGTGATCAGA[C/T]AATAGAAAAAGTATT	7110
rs767246951	in-del	-/A	3.11959e-05	0.0039493	intron-variant	TMF1	GRCh38.p7	3:69027866	ATCTACTAAATGGTT[-/A]ACACCACAAACAAAC	7110
rs767247203	snp	A/T	3.31559e-05	0.00407147	intron-variant	TMF1	GRCh38.p7	3:69034996	ACATACTTCTTGGAT[A/T]TGTGTTTTGGAAACC	7110
rs767302195	in-del	-/CAA			intron-variant	TMF1	GRCh38.p7	3:69051474	AGTGAGACTCCGTCT[-/CAA]CAACAACATAAAACC	7110
rs767336034	snp	A/G/T	5.08103e-05	0.00504014	missense	TMF1	GRCh38.p7	3:69028239	ACCTTTTCTTTCCTC[A/G/T]TCTCTTCAAGTGTTC	7110
rs767342448	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69037813	GTCTCAAAAAATATA[C/T]ATAAATTGAAAAAAA	7110
rs767408395	in-del	-/T	1.80432e-05	0.00300354	intron-variant	TMF1	GRCh38.p7	3:69047345	AAAAATCCCTTCCAC[-/T]TACTAGAGTTACCTT	7110
rs767453295	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69028614	AGATTCCACAAAGCT[C/T]ATTAGGGAGTTCTAT	7110
rs767475029	snp	C/T	3.31994e-05	0.00407414	missense	TMF1	GRCh38.p7	3:69048095	TTTCCATAGTTGTTT[C/T]CACATCAATTACACT	7110
rs767513071	in-del	-/AGTTTATAAATGTTGCC	1.66134e-05	0.00288208	intron-variant	TMF1	GRCh38.p7	3:69038738	TAAAAAATTAGATTG[-/AGTTTATAAATGTTGCC]AGTGATCAGATAATA	7110
rs767530233	snp	C/T	1.68655e-05	0.00290387	missense	TMF1	GRCh38.p7	3:69042900	CAAGTTCTTCTTTTA[C/T]GTTTTTGATTTCCTA	7110
rs767620523	snp	A/G	1.65776e-05	0.00287898	missense	TMF1	GRCh38.p7	3:69047728	ACACTAAATGAGTCT[A/G]TTCTTTCAAAAGCAT	7110
rs767711790	snp	A/G	6.81838e-05	0.00583843	intron-variant	TMF1	GRCh38.p7	3:69033524	AAGAGCTTCTGCATC[A/G]AGCATAAAAACTAAA	7110
rs767720534	snp	C/T	2.22437e-05	0.00333487	intron-variant	TMF1	GRCh38.p7	3:69028013	AGAGAGAAATAAAGT[C/T]AGACAATTTCTGTGA	7110
rs767785094	snp	A/C			intron-variant	TMF1	GRCh38.p7	3:69037850	CAAATCAACACCATA[A/C]TCAGTTACCACTTCA	7110
rs767791918	snp	A/G			missense	TMF1	GRCh38.p7	3:69029911	AAAAGAGAATTCTGT[A/G]ACTCCATGGAAGACA	7110
rs767821183	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69035138	AGGAGAAACAATACA[C/T]TCACAAACAATGGTA	7110
rs767822466	snp	A/C	1.66568e-05	0.00288585	missense	TMF1	GRCh38.p7	3:69047835	AAGCTGAAAAGATGT[A/C]TGCATCAAGTGAAGA	7110
rs767829018	snp	A/C	3.66468e-05	0.00428043	intron-variant	TMF1	GRCh38.p7	3:69047328	CTCCAAAAAGCACAT[A/C]TAAAAATCCCTTCCA	7110
rs767883193	snp	A/T	1.65806e-05	0.00287924	missense	TMF1	GRCh38.p7	3:69047435	CAGCCACCTTGTCTA[A/T]CACAGTCTGTCCTTC	7110
rs767955406	snp	C/T			downstream-variant-500B	TMF1	GRCh38.p7	3:69019343	TAGCACTGTGTTTTC[C/T]GAAAACATATCTTCA	7110
rs767965718	snp	C/T	1.69539e-05	0.00291147	intron-variant	TMF1	GRCh38.p7	3:69025554	CAAATTTAATTTTTC[C/T]AATACCTGTAAATGA	7110
rs768005498	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69027620	TTCCCTGGGCCTCAT[C/T]TGAAGAACAAGAATT	7110
rs768009095	snp	A/T			utr-variant-3-prime	TMF1	GRCh38.p7	3:69020863	ATAAAATTGAAAAGT[A/T]TAGGAATGAGTTTTA	7110
rs768056382	snp	C/T	1.65641e-05	0.00287781	missense	TMF1	GRCh38.p7	3:69047549	CTTCCTCAGTGGGTA[C/T]AACTAATGTTTCATT	7110
rs768097809	snp	A/G	8.45416e-05	0.00650105	intron-variant	TMF1	GRCh38.p7	3:69051914	AACAGCAGCCTCCGG[A/G]AGCCAGGAACCCCGC	7110
rs768103508	snp	C/T	3.44062e-05	0.00414752	intron-variant	TMF1	GRCh38.p7	3:69025953	GCATATTTCCTTTAT[C/T]ATTATTCTAAGAACT	7110
rs768200762	snp	A/G	1.65647e-05	0.00287786	synonymous-codon	TMF1	GRCh38.p7	3:69033606	TGTCTGGGATCCCAG[A/G]GTTGCTTGCAAATTT	7110
rs768362555	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69029287	GATCCACCTGCCTCA[A/G]CCTCCCAAAGTGCTG	7110
rs768365862	snp	A/G	1.66438e-05	0.00288472	missense, downstream-variant-500B	TMF1, MIR3136	GRCh38.p7	3:69048523	GATTTCAACCCCCAG[A/G]TTGAAGTATCCCATC	7110
rs768368424	snp	A/G	1.65996e-05	0.00288089	synonymous-codon	TMF1	GRCh38.p7	3:69033699	ATTCTCTGCTTCCTG[A/G]AGTCTCTGAATCATG	7110
rs768468840	snp	C/T	1.66034e-05	0.00288122	missense	TMF1	GRCh38.p7	3:69038928	GACGGCCAAGATCTT[C/T]CTCTTGGCGTTCTAC	7110
rs768496946	snp	A/G			upstream-variant-2KB	TMF1	GRCh38.p7	3:69052473	ACAGCAGTTCTTAGC[A/G]AAGGGGAAGCTATGG	7110
rs768507952	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69034679	TCTGCATGTTATAAA[C/T]GACTGAAAATTAACA	7110
rs768532667	snp	A/G	1.67441e-05	0.0028934	synonymous-codon	TMF1	GRCh38.p7	3:69038845	TTCATTTTCTTACTT[A/G]TATGCACTATCCAGG	7110
rs768537473	snp	C/T	3.37889e-05	0.00411015	synonymous-codon	TMF1	GRCh38.p7	3:69029841	ATCCTCCAGTTTACA[C/T]AGCCTATTTTTCTCT	7110
rs768596855	snp	A/T	1.65781e-05	0.00287902	synonymous-codon	TMF1	GRCh38.p7	3:69029931	CATGGAAGACATCTG[A/T]ATTTTGTTAGCAAGG	7110
rs768698258	snp	C/T			missense	TMF1	GRCh38.p7	3:69048223	GCTGCCAGAGTTTCC[C/T]CTGAAACACACAAAG	7110
rs768719782	in-del	-/AA			intron-variant	TMF1	GRCh38.p7	3:69027680	AATAGCTGATGAACT[-/AA]AAAAAAAAAAAAAAA	7110
rs768748417	snp	C/T	1.65704e-05	0.00287836	splice-acceptor-variant	TMF1	GRCh38.p7	3:69027994	CTATTCAACAATGTC[C/T]AATAGAGAGAAATAA	7110
rs768748751	snp	A/G			missense	TMF1	GRCh38.p7	3:69047854	ATCAAGTGAAGACTT[A/G]ATTTTGAATCTGTAG	7110
rs768775017	in-del	-/AA			intron-variant	TMF1	GRCh38.p7	3:69033274	GTGAGACTCCATCTC[-/AA]AAAAAAAAAAAAAAA	7110
rs768782185	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69045874	AGACCAGCCTGGCAG[C/T]ATAGTGAGACCTCAT	7110
rs768804033	snp	A/T	1.65875e-05	0.00287984	missense	TMF1	GRCh38.p7	3:69038717	GTGAAGATCAGTAAG[A/T]TCTCTTAAAAAATTA	7110
rs768834828	snp	G/T			missense	TMF1	GRCh38.p7	3:69025697	TTGGTCCAAATGAGT[G/T]ATCATGAGACTCATC	7110
rs768851779	in-del	-/T	3.3644e-05	0.00410132	frameshift-variant	TMF1	GRCh38.p7	3:69024066	TTACTCTTAGCTGAG[-/T]TCTAAGTTTGGGTAT	7110
rs769085795	snp	C/T	1.68162e-05	0.00289962	synonymous-codon	TMF1	GRCh38.p7	3:69028256	CTCTTCAAGTGTTCT[C/T]ACATATTCATCTTTT	7110
rs769176987	snp	A/G	3.31972e-05	0.004074	intron-variant	TMF1	GRCh38.p7	3:69042792	TTTTCATAGTCAACC[A/G]AATACTATACGCACC	7110
rs769210782	in-del	-/A			intron-variant	TMF1	GRCh38.p7	3:69028042	ATAGTAATTCATGCC[-/A]ATGATAAGTCAATCT	7110
rs769213445	snp	C/G	1.66161e-05	0.00288232	synonymous-codon, downstream-variant-500B	TMF1, MIR3136	GRCh38.p7	3:69048516	AGTGTTTGATTTCAA[C/G]CCCCAGGTTGAAGTA	7110
rs769230232	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69026822	ATAAAATTACTAATG[A/G]GTGTTACAAATCATA	7110
rs769312862	snp	A/G	3.31411e-05	0.00407056	missense	TMF1	GRCh38.p7	3:69033586	TCTAATTTCTCCCAC[A/G]ACGATGTCTGGGATC	7110
rs769314463	snp	A/C	1.71911e-05	0.00293177	intron-variant	TMF1	GRCh38.p7	3:69024229	AAACATATCTTTTTT[A/C]ATACTCCCAGTAATA	7110
rs769353050	snp	A/G	3.33968e-05	0.00408623	missense	TMF1	GRCh38.p7	3:69047887	TCTTGTCTCGAGCTC[A/G]CTGAGCTCTCACTTA	7110
rs769418982	snp	C/T			intron-variant, upstream-variant-2KB	TMF1, MIR3136	GRCh38.p7	3:69049990	TCAGGCCAGGCGCAG[C/T]GGCTCACGCTTGTAA	7110
rs769534570	snp	A/C			utr-variant-3-prime	TMF1	GRCh38.p7	3:69020285	ATCTTAAGTCACAAC[A/C]TAGATATATTTGGTA	7110
rs769543893	snp	A/G	0.000187459	0.00967958	intron-variant	TMF1	GRCh38.p7	3:69042307	CCTCCCCAAGTGCTG[A/G]GATTACAGTCATAAG	7110
rs769548331	in-del	-/TAC	0.000135217	0.00822134	intron-variant	TMF1	GRCh38.p7	3:69030013	TGGGATTCACCTGAT[-/TAC]AGGACAGAAAAAAAA	7110
rs769607190	snp	C/T	3.31241e-05	0.00406952	missense	TMF1	GRCh38.p7	3:69047512	ACAGGAGTTGCACTT[C/T]GTCCACTTTCTTCCA	7110
rs769648729	snp	C/T	1.65704e-05	0.00287836	missense	TMF1	GRCh38.p7	3:69025643	CTGCTCCCATCCTTA[C/T]AGCATCATAAAGATT	7110
rs769684907	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69041477	CAACTGTTCTCAAAC[A/G]CTACCCTTTCTCTGG	7110
rs769686540	snp	A/C	1.6612e-05	0.00288196	intron-variant	TMF1	GRCh38.p7	3:69038738	TAAAAAATTAGATTG[A/C]GTTTATAAATGTTGC	7110
rs769738701	snp	A/G	1.67899e-05	0.00289736	intron-variant	TMF1	GRCh38.p7	3:69038823	TTCTAAATGGGTTGC[A/G]TATTTGTTCATTTTC	7110
rs769742751	snp	A/G	1.67913e-05	0.00289748	synonymous-codon	TMF1	GRCh38.p7	3:69028273	CATATTCATCTTTTA[A/G]GTTTTCCAATTCAAC	7110
rs769780303	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69042199	GCACCACCACCACCC[A/G]GCTAATTTTTGTATT	7110
rs769842459	snp	C/T	0.000156979	0.00885804	intron-variant	TMF1	GRCh38.p7	3:69043917	TGAGGATGGTGTCTA[C/T]ATATCCCAAAGGTAT	7110
rs769844282	in-del	-/C			intron-variant	TMF1	GRCh38.p7	3:69026167	AAAGCAAGAACATTT[-/C]CTAGGGTTAATGAGA	7110
rs769889654	snp	C/T	1.65842e-05	0.00287955	intron-variant	TMF1	GRCh38.p7	3:69035149	TACATTCACAAACAA[C/T]GGTACAGTATTATCT	7110
rs769890758	snp	C/T			utr-variant-3-prime	TMF1	GRCh38.p7	3:69022996	AATAAAGTTCAAATA[C/T]TGCACAAAATAATTT	7110
rs769911515	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69035585	GGCCATCCTAGTCTT[A/G]GGAATTCACTCTAAG	7110
rs769947418	snp	C/T	0.000165832	0.00910431	synonymous-codon	TMF1	GRCh38.p7	3:69048135	TTTCAAACTTACAGT[C/T]GGCACCTTCATATCC	7110
rs769975460	snp	A/G	4.96808e-05	0.00498377	missense	TMF1	GRCh38.p7	3:69048289	GTTCTTGACTGGCCA[A/G]TGTGCAAGGATTCAT	7110
rs769984015	snp	A/G	2.46084e-05	0.00350765	intron-variant	TMF1	GRCh38.p7	3:69023365	AAATAACTACACAGA[A/G]CATCTTTAATATTTA	7110
rs770038235	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69051595	ATCCCAACAGTGCCC[A/G]AGACGCGAAGCAATT	7110
rs770046524	snp	A/G	2.09453e-05	0.00323608	synonymous-codon	TMF1	GRCh38.p7	3:69027986	CTAACTGACTATTCA[A/G]CAATGTCTAATAGAG	7110
rs770067424	snp	C/T	1.8083e-05	0.00300686	intron-variant	TMF1	GRCh38.p7	3:69043743	TATTACTTTAAATTT[C/T]AATTACCTTTTTAGC	7110
rs770131669	in-del	-/AT			intron-variant	TMF1	GRCh38.p7	3:69031437	CACACACACACACAT[-/AT]ACACAAATGAGTACC	7110
rs770232399	snp	G/T	1.66125e-05	0.00288201	missense	TMF1	GRCh38.p7	3:69047784	TTTTTGGAAATCATC[G/T]AAACGATTATATTCA	7110
rs770246456	in-del	-/ATT	1.77351e-05	0.00297779	intron-variant	TMF1	GRCh38.p7	3:69044466	CAGAAAATGTGTAAC[-/ATT]ATTCACATTTGCAGA	7110
rs770275016	snp	C/T	1.72877e-05	0.00293999	intron-variant	TMF1	GRCh38.p7	3:69026147	GAGCAAAGAGATAAG[C/T]AGAGAAAGCAAGAAC	7110
rs770404957	snp	C/G			intron-variant	TMF1	GRCh38.p7	3:69032693	TCAGCTCACTGCAGC[C/G]TCTGCTTCCCAGGTT	7110
rs770457737	snp	C/T	1.78159e-05	0.00298457	intron-variant	TMF1	GRCh38.p7	3:69030045	AATCACATACACATA[C/T]AGCCCAGAGACCAAA	7110
rs770580394	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69038425	AAAAACACAACTGGT[C/T]AAATTTAGCAGAATC	7110
rs770624563	in-del	-/AGTC	1.70983e-05	0.00292384	intron-variant	TMF1	GRCh38.p7	3:69044618	AGGCGAATACATAAA[-/AGTC]AGAACGCTTAGCTTT	7110
rs770631381	snp	C/G	3.33406e-05	0.00408279	missense	TMF1	GRCh38.p7	3:69038948	TGGCGTTCTACCATG[C/G]AATTTAGTTTTTTAA	7110
rs770632577	snp	C/G			utr-variant-5-prime	TMF1	GRCh38.p7	3:69052309	ATGCGCTTGCTTCTT[C/G]CACGTACACAGCAAC	7110
rs770670657	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69042375	TTCAGAGACAAAAGT[A/G]CTTAATAATTTAAAA	7110
rs770707299	snp	C/T	5.10877e-05	0.00505384	intron-variant	TMF1	GRCh38.p7	3:69024221	TTAAATCAAAACATA[C/T]CTTTTTTAATACTCC	7110
rs770709960	snp	G/T			intron-variant	TMF1	GRCh38.p7	3:69043265	GCCTCAACCTCCCAG[G/T]CTCAGGTGATCCTCC	7110
rs770715786	snp	G/T	3.39242e-05	0.00411837	synonymous-codon	TMF1	GRCh38.p7	3:69024057	GAAGAATACTTACTC[G/T]TAGCTGAGTTCTAAG	7110
rs770794140	snp	C/T	3.3129e-05	0.00406982	missense	TMF1	GRCh38.p7	3:69038611	CTTCTTCTTGGGCCT[C/T]CTCTAATGCTGCAGA	7110
rs770795198	snp	A/C	1.65778e-05	0.002879	missense	TMF1	GRCh38.p7	3:69033579	ATTCTTCTCTAATTT[A/C]TCCCACGACGATGTC	7110
rs770829431	snp	A/G	3.42513e-05	0.00413817	intron-variant	TMF1	GRCh38.p7	3:69044619	GGCGAATACATAAAA[A/G]TCAGAACGCTTAGCT	7110
rs770847331	snp	G/T			intron-variant	TMF1	GRCh38.p7	3:69039952	TTTTAAAGAGAAAAA[G/T]CTGGCAGTCAACTCC	7110
rs770884617	snp	C/T	5.2198e-05	0.00510845	synonymous-codon	TMF1	GRCh38.p7	3:69047370	TACCTTGCAAACATC[C/T]TCCTTCTCAGAAAGT	7110
rs770904242	snp	G/T			intron-variant	TMF1	GRCh38.p7	3:69030996	GCTTGGAATCAGCCT[G/T]GACGTCCCTTGTGCA	7110
rs770944463	snp	A/G	3.31521e-05	0.00407123	missense	TMF1	GRCh38.p7	3:69048151	GGCACCTTCATATCC[A/G]ATTCTTTATTAACAG	7110
rs771018932	snp	C/T			utr-variant-3-prime	TMF1	GRCh38.p7	3:69020668	AGTTTTTCAAGAAAC[C/T]GTTTAAGTTCACTTT	7110
rs771027317	in-del	-/TTTA			intron-variant	TMF1	GRCh38.p7	3:69042036	TGCTATTAATTTTAT[-/TTTA]TTTATTTATTTTTTT	7110
rs771029555	snp	C/T	1.65605e-05	0.0028775	missense	TMF1	GRCh38.p7	3:69048434	AATTTTCAGATTCAT[C/T]GACCACAGTCCTCCG	7110
rs771065230	snp	C/T			utr-variant-3-prime	TMF1	GRCh38.p7	3:69021513	AAGAATATTTATTAA[C/T]ACTACCAATCAGAGA	7110
rs771086763	snp	G/T			intron-variant	TMF1	GRCh38.p7	3:69037257	CCCCGCACTTTGGGA[G/T]GCCAAGGCAGGCGGA	7110
rs771088565	snp	A/G	1.75823e-05	0.00296493	missense	TMF1	GRCh38.p7	3:69023185	TCACAAGTTAACTGA[A/G]ACTTTGTCTTAAAAG	7110
rs771139026	snp	A/G	1.67933e-05	0.00289765	synonymous-codon	TMF1	GRCh38.p7	3:69052072	GGAGAGCTGGGAGGC[A/G]TTGAACCAACTCATC	7110
rs771167739	snp	A/G	1.6571e-05	0.0028784	intron-variant	TMF1	GRCh38.p7	3:69035132	TGTAGGAGGAGAAAC[A/G]ATACATTCACAAACA	7110
rs771201238	snp	G/T			intron-variant	TMF1	GRCh38.p7	3:69035817	CTATAAAATAACACG[G/T]AAGACATCAATTATG	7110
rs771208458	snp	A/C	3.31356e-05	0.00407022	missense	TMF1	GRCh38.p7	3:69047657	AAGCATATCCCTTGC[A/C]TGACAATTCATCATC	7110
rs771214047	snp	A/G	1.66192e-05	0.00288259	synonymous-codon	TMF1	GRCh38.p7	3:69048072	CTGCGTAGACGTATT[A/G]GATATACTTTCCATA	7110
rs771219527	snp	C/G	1.70971e-05	0.00292374	missense	TMF1	GRCh38.p7	3:69029831	TATTGTTCTCATCCT[C/G]CAGTTTACACAGCCT	7110
rs771220648	snp	C/T	1.68148e-05	0.0028995	intron-variant	TMF1	GRCh38.p7	3:69026127	AAAATTCTGTTCATA[C/T]TAAAGAGCAAAGAGA	7110
rs771294958	snp	A/G	1.65787e-05	0.00287907	missense	TMF1	GRCh38.p7	3:69026003	AACATCACCTGAGAC[A/G]GAAAAGATGTCTGTA	7110
rs771340707	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69023604	TTAATGTAAGCACAC[C/T]TGATATAAAATTTAG	7110
rs771383317	snp	A/C			intron-variant	TMF1	GRCh38.p7	3:69046948	TAAACATGTAAAAAC[A/C]AATTCTGATACAAGA	7110
rs771442384	in-del	-/AA			intron-variant	TMF1	GRCh38.p7	3:69044615	ATAAGGCGAATACAT[-/AA]AAGTCAGAACGCTTA	7110
rs771443525	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69039987	CTAAGCATTCAGTTT[C/T]GGCATCACCAATTGT	7110
rs771459766	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69035896	CAGTACTTGGAAAAA[A/G]TGATGGATTTATGCA	7110
rs771481761	snp	C/T	1.71457e-05	0.0029279	intron-variant	TMF1	GRCh38.p7	3:69043889	TCACTAAATTTAAAA[C/T]AATATTTGAGAATGA	7110
rs771499690	in-del	-/A			upstream-variant-2KB	TMF1	GRCh38.p7	3:69053584	AATTATTTTTCTTTT[-/A]AAAAAATCAGATTGA	7110
rs771549396	snp	A/G	3.3134e-05	0.00407012	synonymous-codon	TMF1	GRCh38.p7	3:69047646	AATAGGCACTAAAGC[A/G]TATCCCTTGCCTGAC	7110
rs771579360	snp	C/T	1.65605e-05	0.0028775	missense	TMF1	GRCh38.p7	3:69048334	ACTTCTTCTTCTGGT[C/T]GTTGTGATTTTGCTG	7110
rs771727208	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69026249	TCAAAAGAAGAAAAA[A/G]AACTTTTTTAAGATT	7110
rs771779990	snp	C/T	1.65647e-05	0.00287786	missense	TMF1	GRCh38.p7	3:69047558	TGGGTATAACTAATG[C/T]TTCATTTACTTCTTC	7110
rs771783869	snp	C/T	1.67913e-05	0.00289748	intron-variant	TMF1	GRCh38.p7	3:69025978	AGAACTAAGCACATA[C/T]AAAAAATAAAACATC	7110
rs771795347	snp	A/C	1.66427e-05	0.00288462	missense	TMF1	GRCh38.p7	3:69052041	GGGCCTGGGACAGGG[A/C]CTGCTTAGCGAAGCT	7110
rs771806553	snp	A/C			intron-variant	TMF1	GRCh38.p7	3:69033093	ACAAGAAAAAAAAAT[A/C]GAGTGCAGCAGTCTA	7110
rs771850302	snp	G/T	1.65803e-05	0.00287922	missense	TMF1	GRCh38.p7	3:69029934	GGAAGACATCTGAAT[G/T]TTGTTAGCAAGGAGT	7110
rs771895905	snp	C/T	1.75329e-05	0.00296077	intron-variant	TMF1	GRCh38.p7	3:69030035	CAGAAAAAAAAATCA[C/T]ATACACATACAGCCC	7110
rs771896549	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69044958	TATAAGAATACTTTA[C/T]GTAGCTTCCTGGTAA	7110
rs771896637	snp	C/G			intron-variant	TMF1	GRCh38.p7	3:69031104	CAACTGTGTGAACCT[C/G]TTCCTGGGAATTACA	7110
rs771945102	snp	C/G	1.65605e-05	0.0028775	missense	TMF1	GRCh38.p7	3:69048309	CAAGGATTCATGTAA[C/G]CTGCTTTTCACTTCT	7110
rs771952884	snp	C/G	1.78544e-05	0.00298779	intron-variant	TMF1	GRCh38.p7	3:69024023	AATGAACTAAAATAT[C/G]TTAGACTCATCCTTA	7110
rs771971795	snp	G/T			downstream-variant-500B	TMF1	GRCh38.p7	3:69019340	TCTTAGCACTGTGTT[G/T]TCCGAAAACATATCT	7110
rs771997538	snp	C/T	1.67024e-05	0.0028898	missense	TMF1	GRCh38.p7	3:69047908	CTCTCACTTATTACA[C/T]TTTCATGATCTAAAA	7110
rs772022897	snp	A/G	0.000132477	0.00813761	missense	TMF1	GRCh38.p7	3:69048407	CAGTTGGCGAGAGAA[A/G]GGCACTGAAGAAATT	7110
rs772042333	snp	C/T	1.68015e-05	0.00289836	synonymous-codon	TMF1	GRCh38.p7	3:69028262	AAGTGTTCTTACATA[C/T]TCATCTTTTAGGTTT	7110
rs772183916	in-del	-/ATTTTT			intron-variant	TMF1	GRCh38.p7	3:69043171	TTAACTTTCCTTTTC[-/ATTTTT]ATTTTTATTTTTTGA	7110
rs772268910	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69043449	AGCTGTGACCACAGG[C/T]GCACACCAGCATGAC	7110
rs772344809	snp	C/T	1.67483e-05	0.00289377	intron-variant	TMF1	GRCh38.p7	3:69051941	CCGCTCCTCTCTCTC[C/T]TACCCGGCTCTCCAT	7110
rs772345743	snp	C/T			utr-variant-3-prime	TMF1	GRCh38.p7	3:69021805	CCTGCCTCAGCCTCC[C/T]GAGTAGCTAGGATTA	7110
rs772399787	in-del	-/A			intron-variant	TMF1	GRCh38.p7	3:69035797	TATACTATTAAATGG[-/A]AAAACTATAAAATAA	7110
rs772445278	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69036137	AAAGTATTATAAAAC[C/T]GTAAAGAGATATTTT	7110
rs772534383	snp	C/G	1.66346e-05	0.00288393	intron-variant	TMF1	GRCh38.p7	3:69033720	CTGAATCATGAAATT[C/G]TGAAGTCATTACCAA	7110
rs772589382	snp	A/G	1.66349e-05	0.00288395	missense	TMF1	GRCh38.p7	3:69025693	GGCATTGGTCCAAAT[A/G]AGTGATCATGAGACT	7110
rs772589423	snp	A/T	1.65616e-05	0.00287759	missense	TMF1	GRCh38.p7	3:69035039	TGCTGAAGTTCACCG[A/T]TCTCATGGCGTAAAT	7110
rs772606655	in-del	-/TT	2.0714e-05	0.00321816	intron-variant	TMF1	GRCh38.p7	3:69023333	ATCCTGAAAAATGTA[-/TT]TGTTTACAATTTTTA	7110
rs772646032	snp	A/C	3.32973e-05	0.00408014	missense	TMF1	GRCh38.p7	3:69038943	TCTCTTGGCGTTCTA[A/C]CATGGAATTTAGTTT	7110
rs772698238	snp	C/T	1.65842e-05	0.00287955	intron-variant	TMF1	GRCh38.p7	3:69042802	CAACCAAATACTATA[C/T]GCACCTTCTTCCATT	7110
rs772719322	snp	A/T			intron-variant, downstream-variant-500B	TMF1, MIR3136	GRCh38.p7	3:69048640	CATTATAAATCAGTA[A/T]AAATATAAATTTAGA	7110
rs772821830	snp	C/G	3.31279e-05	0.00406975	missense	TMF1	GRCh38.p7	3:69047567	CTAATGTTTCATTTA[C/G]TTCTTCAGATTTTCC	7110
rs772826421	snp	A/G	1.77786e-05	0.00298144	intron-variant	TMF1	GRCh38.p7	3:69044459	AGGTTTCCAGAAAAT[A/G]TGTAACATTATTCAC	7110
rs772832032	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69037620	GCACTCCAGCCTGGG[C/T]AACAAGAGCGAAACT	7110
rs772834560	snp	C/T	1.76999e-05	0.00297483	intron-variant	TMF1	GRCh38.p7	3:69024029	CTAAAATATCTTAGA[C/T]TCATCCTTAGGTGAA	7110
rs772876814	snp	A/T	3.31351e-05	0.00407019	synonymous-codon	TMF1	GRCh38.p7	3:69047649	AGGCACTAAAGCATA[A/T]CCCTTGCCTGACAAT	7110
rs772910727	snp	C/T			intron-variant, upstream-variant-2KB	TMF1, MIR3136	GRCh38.p7	3:69049995	CCAGGCGCAGTGGCT[C/T]ACGCTTGTAATCTCA	7110
rs773003630	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69037217	GAATGCAAATCAGCC[A/G]GGCGTAGTGGCTCAC	7110
rs773059425	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69041117	AAAATAATAACATTC[A/G]ATATTAATATTTCAA	7110
rs773079006	snp	C/G	0.000186133	0.0096453	intron-variant	TMF1	GRCh38.p7	3:69042335	AAGCCACCACACTCA[C/G]CCAACCCTGTTTATT	7110
rs773193492	snp	C/G			intron-variant	TMF1	GRCh38.p7	3:69034860	TTGTATAATTTTTAA[C/G]GTGCCCACTCTGATT	7110
rs773243297	snp	C/T	1.76521e-05	0.00297081	missense	TMF1	GRCh38.p7	3:69023250	TCTTCGAGATCTAAT[C/T]GAAGTTCTTCTGCCT	7110
rs773261472	snp	A/G	3.31252e-05	0.00406958	missense	TMF1	GRCh38.p7	3:69048199	TCAGTTTTAGGTGAT[A/G]AAGTACCTGCTGCCA	7110
rs773264428	snp	A/C			intron-variant	TMF1	GRCh38.p7	3:69039397	GTGAGCCACCCCACT[A/C]GGCTAAAAAATCTTA	7110
rs773314310	snp	C/T	1.65605e-05	0.0028775	missense	TMF1	GRCh38.p7	3:69048310	AAGGATTCATGTAAG[C/T]TGCTTTTCACTTCTT	7110
rs773438070	snp	A/C			upstream-variant-2KB	TMF1	GRCh38.p7	3:69053910	GAATTATTATAGCAC[A/C]TATATGGTGCTAAAT	7110
rs773459052	snp	C/T	1.76621e-05	0.00297165	synonymous-codon	TMF1	GRCh38.p7	3:69023261	TAATCGAAGTTCTTC[C/T]GCCTCTTCTGCTTTT	7110
rs773478687	snp	A/C			utr-variant-3-prime	TMF1	GRCh38.p7	3:69020477	TCATTTTTTTATATT[A/C]TTGAAAATGTTATTT	7110
rs773515795	snp	A/G	1.67038e-05	0.00288992	synonymous-codon	TMF1	GRCh38.p7	3:69047913	ACTTATTACACTTTC[A/G]TGATCTAAAACTTCA	7110
rs773588897	snp	A/G	1.65616e-05	0.00287759	synonymous-codon	TMF1	GRCh38.p7	3:69035044	AAGTTCACCGATCTC[A/G]TGGCGTAAATAATCC	7110
rs773673201	snp	C/T	1.66788e-05	0.00288775	missense	TMF1	GRCh38.p7	3:69051951	CTCTCTTACCCGGCT[C/T]TCCATACGGAATGGT	7110
rs773673945	snp	A/G	3.32685e-05	0.00407837	missense	TMF1	GRCh38.p7	3:69025694	GCATTGGTCCAAATG[A/G]GTGATCATGAGACTC	7110
rs773725323	snp	A/C	1.6607e-05	0.00288153	splice-donor-variant	TMF1	GRCh38.p7	3:69025994	AAAAAATAAAACATC[A/C]CCTGAGACAGAAAAG	7110
rs773733808	in-del	-/A	1.74897e-05	0.00295712	intron-variant	TMF1	GRCh38.p7	3:69044636	AGAACGCTTAGCTTT[-/A]AAAAAAGACCATTTT	7110
rs773737233	in-del	-/T	1.66181e-05	0.00288249	frameshift-variant	TMF1	GRCh38.p7	3:69044544	TTCCTTACTAAGAGA[-/T]TAATAACTGAGCCTC	7110
rs773763239	in-del	-/ATCC			intron-variant	TMF1	GRCh38.p7	3:69045958	TACTAGAGCGGATTA[-/ATCC]GGTGGGAGGACTGCT	7110
rs773792115	snp	A/C	1.65638e-05	0.00287778	stop-gained	TMF1	GRCh38.p7	3:69047554	TCAGTGGGTATAACT[A/C]ATGTTTCATTTACTT	7110
rs773835562	snp	A/T			intron-variant	TMF1	GRCh38.p7	3:69046611	AAGATACCAGATCCA[A/T]CTAAATTTGTATATC	7110
rs773844072	snp	G/T			intron-variant	TMF1	GRCh38.p7	3:69039880	TTGGGTAAAAGGTTG[G/T]TGGGAACTGGATATT	7110
rs773917764	snp	A/C	1.66134e-05	0.00288208	missense	TMF1	GRCh38.p7	3:69025690	ATAGGCATTGGTCCA[A/C]ATGAGTGATCATGAG	7110
rs773919339	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69045707	ATCACTTGAACCTGG[A/G]AGGCAGACTAGCCTG	7110
rs773928400	in-del	-/A	1.70214e-05	0.00291726	intron-variant	TMF1	GRCh38.p7	3:69038526	GAAGCATAAACAAAT[-/A]TTTTTAAAACTACTC	7110
rs773938151	snp	C/G			intron-variant	TMF1	GRCh38.p7	3:69030406	TTAGGAAAAAACAGA[C/G]GAGAAAGTCTTCAGG	7110
rs773958491	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69031000	GGAATCAGCCTGGAC[A/G]TCCCTTGTGCAGTGA	7110
rs773961705	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69024355	CAGTGGCAGAAAAAC[A/G]GTCCCAACTTTCCTG	7110
rs773979278	snp	A/C/T	3.31599e-05	0.00407174	missense	TMF1	GRCh38.p7	3:69029933	TGGAAGACATCTGAA[A/C/T]TTTGTTAGCAAGGAG	7110
rs773980296	snp	C/T	4.99513e-05	0.00499731	missense, downstream-variant-500B	TMF1, MIR3136	GRCh38.p7	3:69048524	ATTTCAACCCCCAGG[C/T]TGAAGTATCCCATCC	7110
rs773997725	snp	C/G	1.68778e-05	0.00290493	intron-variant	TMF1	GRCh38.p7	3:69051921	GCCTCCGGGAGCCAG[C/G]AACCCCGCTCCTCTC	7110
rs774044003	snp	C/G/T	8.54831e-05	0.00653721	intron-variant	TMF1	GRCh38.p7	3:69025548	CTATAGCAAATTTAA[C/G/T]TTTTCCAATACCTGT	7110
rs774070834	snp	C/G	1.65669e-05	0.00287805	missense	TMF1	GRCh38.p7	3:69048177	AACAGTTTCTTCGTG[C/G]TTGCCTTCAGTTTTA	7110
rs774163292	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69043313	TAGTTGGGACCACAC[A/G]CATGTACCACCATGG	7110
rs774339640	snp	A/C	1.67357e-05	0.00289268	missense	TMF1	GRCh38.p7	3:69038850	TTTCTTACTTGTATG[A/C]ACTATCCAGGGCAGC	7110
rs774378027	snp	A/G	2.16856e-05	0.00329277	intron-variant	TMF1	GRCh38.p7	3:69028000	AACAATGTCTAATAG[A/G]GAGAAATAAAGTTAG	7110
rs774392877	snp	C/G	1.68374e-05	0.00290145	missense	TMF1	GRCh38.p7	3:69029844	CTCCAGTTTACACAG[C/G]CTATTTTTCTCTGAT	7110
rs774431119	snp	A/G			upstream-variant-2KB	TMF1	GRCh38.p7	3:69054114	AACTGCCATATCTAA[A/G]TCAAAAACAAAGAAT	7110
rs774434901	snp	C/T	3.31884e-05	0.00407346	intron-variant	TMF1	GRCh38.p7	3:69035157	CAAACAATGGTACAG[C/T]ATTATCTATAACTTC	7110
rs774516145	snp	A/G			utr-variant-3-prime	TMF1	GRCh38.p7	3:69021623	TCTTCAAGATGGTGT[A/G]CTTGTATCTATATTC	7110
rs774547838	snp	C/T	1.66335e-05	0.00288383	missense	TMF1	GRCh38.p7	3:69047807	TATATTCAGGACAAG[C/T]AGATGCAGAGAGAAG	7110
rs774584932	snp	A/T			intron-variant	TMF1	GRCh38.p7	3:69047096	AAGTGATAAGGACTC[A/T]AAAATAAAGATGTAA	7110
rs774682939	snp	A/C	1.65655e-05	0.00287793	stop-gained	TMF1	GRCh38.p7	3:69038602	GCTGACGGGCTTCTT[A/C]TTGGGCCTTCTCTAA	7110
rs774689435	snp	A/G	1.67022e-05	0.00288978	synonymous-codon	TMF1	GRCh38.p7	3:69047898	GCTCGCTGAGCTCTC[A/G]CTTATTACACTTTCA	7110
rs774903275	snp	A/C			intron-variant, upstream-variant-2KB	TMF1, MIR3136	GRCh38.p7	3:69049193	CTGGGCAACATAGTG[A/C]GACCCCTGTCCCTAC	7110
rs774916383	snp	C/T	1.74449e-05	0.00295332	intron-variant	TMF1	GRCh38.p7	3:69044633	AGTCAGAACGCTTAG[C/T]TTTAAAAAAGACCAT	7110
rs774937509	snp	A/C	1.75173e-05	0.00295945	intron-variant	TMF1	GRCh38.p7	3:69025510	AGGGTGCTATTTATT[A/C]GGCCTCAAAACTTCA	7110
rs774975354	snp	G/T			intron-variant	TMF1	GRCh38.p7	3:69027499	TCAAAATTACTTTGG[G/T]TCCACTCTGAGCAGG	7110
rs774981011	snp	A/G			missense	TMF1	GRCh38.p7	3:69048352	TGTGATTTTGCTGGA[A/G]GTTTTGATACCACTG	7110
rs775000257	snp	A/G	0.000186237	0.009648	intron-variant	TMF1	GRCh38.p7	3:69042315	AGTGCTGAGATTACA[A/G]TCATAAGCCACCACA	7110
rs775021218	snp	C/T	0.00148782	0.0272341	intron-variant	TMF1	GRCh38.p7	3:69042381	GACAAAAGTGCTTAA[C/T]AATTTAAAAATTAAT	7110
rs775050943	snp	C/T	6.628e-05	0.00575635	synonymous-codon	TMF1	GRCh38.p7	3:69033588	TAATTTCTCCCACGA[C/T]GATGTCTGGGATCCC	7110
rs775055731	snp	A/G	9.93855e-05	0.00704861	intron-variant	TMF1	GRCh38.p7	3:69035019	TGGAAACCTGTGACA[A/G]TACCTGCTGAAGTTC	7110
rs775070854	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69039998	GTTTTGGCATCACCA[A/G]TTGTAGTACAGCCTG	7110
rs775118045	snp	C/G	1.6625e-05	0.00288309	missense, downstream-variant-500B	TMF1, MIR3136	GRCh38.p7	3:69048519	GTTTGATTTCAACCC[C/G]CAGGTTGAAGTATCC	7110
rs775271991	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69026385	GTGGATCACCTGAGG[C/T]TGGGAGATCAAGACC	7110
rs775295932	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69033101	AAAAAATCGAGTGCA[A/G]CAGTCTACTAAAAAT	7110
rs775356915	snp	A/C	1.68145e-05	0.00289948	missense	TMF1	GRCh38.p7	3:69028280	ATCTTTTAGGTTTTC[A/C]AATTCAACCTGGTAC	7110
rs775358528	snp	C/T	1.67837e-05	0.00289682	intron-variant	TMF1	GRCh38.p7	3:69038826	TAAATGGGTTGCATA[C/T]TTGTTCATTTTCTTA	7110
rs775363372	in-del	-/C	1.79641e-05	0.00299696	intron-variant, splice-donor-variant	TMF1	GRCh38.p7	3:69047348	AATCCCTTCCACTTA[-/C]TAGAGTTACCTTGCA	7110
rs775446201	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69045236	GCTGAGGTGGGGGGA[C/T]CACCTGAGGTCAGGA	7110
rs775479634	snp	A/G	1.65899e-05	0.00288005	intron-variant	TMF1	GRCh38.p7	3:69035155	CACAAACAATGGTAC[A/G]GTATTATCTATAACT	7110
rs775520031	snp	C/T			upstream-variant-2KB	TMF1	GRCh38.p7	3:69052451	TATTGATGTCGATTT[C/T]GTGCTTACAGCAGTT	7110
rs775636518	snp	C/G			intron-variant	TMF1	GRCh38.p7	3:69051501	AAAACCACATTACGC[C/G]CTACCAAGCGCGAAA	7110
rs775723981	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69036251	TAAACTATCATTTAC[A/G]TAAAAAGGATGTAGG	7110
rs775755274	snp	G/T	1.71111e-05	0.00292494	utr-variant-5-prime	TMF1	GRCh38.p7	3:69052102	CGCCCCTCCTCAGCC[G/T]GCAGTGGCGGCGGCA	7110
rs775757767	snp	G/T			intron-variant	TMF1	GRCh38.p7	3:69043467	ACACCAGCATGACCA[G/T]CTAACTTTATGTATT	7110
rs775898011	in-del	-/CTTA	1.78541e-05	0.00298776	intron-variant	TMF1	GRCh38.p7	3:69024022	AATGAACTAAAATAT[-/CTTA]CTTAGACTCATCCTT	7110
rs775959968	snp	C/G	1.73797e-05	0.0029478	intron-variant	TMF1	GRCh38.p7	3:69026149	GCAAAGAGATAAGCA[C/G]AGAAAGCAAGAACAT	7110
rs776050216	snp	A/G	5.52379e-05	0.00525508	intron-variant	TMF1	GRCh38.p7	3:69030059	ACAGCCCAGAGACCA[A/G]AATACCAAGTCAATT	7110
rs776065417	snp	C/T	1.65605e-05	0.0028775	missense	TMF1	GRCh38.p7	3:69048325	CTGCTTTTCACTTCT[C/T]CTTCTGGTCGTTGTG	7110
rs776096305	snp	A/T			synonymous-codon	TMF1	GRCh38.p7	3:69048453	CACAGTCCTCCGAAC[A/T]GGCTTTGTGATTGCT	7110
rs776112655	snp	C/T	1.65982e-05	0.00288077	synonymous-codon	TMF1	GRCh38.p7	3:69047769	GCAACTCTCAGTGAG[C/T]TTTTGGAAATCATCT	7110
rs776113153	snp	C/T			utr-variant-3-prime	TMF1	GRCh38.p7	3:69021948	CTTGGCCTCCCAAAG[C/T]GCTGGGATTACAGGC	7110
rs776115228	snp	C/G	1.65723e-05	0.00287852	missense	TMF1	GRCh38.p7	3:69047692	TTGATTTCACTTACA[C/G]TCCGGCTATCTAATG	7110
rs776154493	in-del	-/A			intron-variant	TMF1	GRCh38.p7	3:69040922	GTGAGACTCTGTTTC[-/A]AAAAAAAAAAAAAAA	7110
rs776167537	snp	A/G	1.67925e-05	0.00289758	intron-variant	TMF1	GRCh38.p7	3:69039522	AAGTAATAACAATAT[A/G]TATGTAGAGAATTAT	7110
rs776170016	snp	C/T	0.000199432	0.00998379	missense	TMF1	GRCh38.p7	3:69047794	TCATCTAAACGATTA[C/T]ATTCAGGACAAGCAG	7110
rs776197372	snp	A/C			utr-variant-3-prime	TMF1	GRCh38.p7	3:69020811	AACTATGTAACTAGA[A/C]ATTGTTAATACGGAT	7110
rs776287027	in-del	-/CTAA			upstream-variant-2KB	TMF1	GRCh38.p7	3:69053331	GTTAAAGACAAAATC[-/CTAA]CTAAAAGCCAGATTT	7110
rs776344528	snp	G/T	3.33968e-05	0.00408623	synonymous-codon	TMF1	GRCh38.p7	3:69038953	TTCTACCATGGAATT[G/T]AGTTTTTTAATATTT	7110
rs776416094	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69037028	ACAAATCCTATATCT[A/G]ATAAAGGTCTAGTAT	7110
rs776497116	snp	A/G			upstream-variant-2KB	TMF1	GRCh38.p7	3:69053553	TTTACCCCACTGCAA[A/G]GAACTCTGCAAAAAA	7110
rs776578404	snp	C/T			upstream-variant-2KB	TMF1	GRCh38.p7	3:69052506	ACCGATAGAGGTCGA[C/T]TTCCCCGGAAGGAAT	7110
rs776588989	snp	A/C	1.7067e-05	0.00292117	intron-variant	TMF1	GRCh38.p7	3:69024222	TAAATCAAAACATAT[A/C]TTTTTTAATACTCCC	7110
rs776622988	snp	A/G	9.93575e-05	0.00704761	missense	TMF1	GRCh38.p7	3:69048439	TCAGATTCATCGACC[A/G]CAGTCCTCCGAACTG	7110
rs776630158	snp	A/C	1.81655e-05	0.0030137	intron-variant	TMF1	GRCh38.p7	3:69043739	TTAATATTACTTTAA[A/C]TTTCAATTACCTTTT	7110
rs776682311	snp	C/T	1.69666e-05	0.00291256	missense	TMF1	GRCh38.p7	3:69044496	AGAATACTTACTCTT[C/T]CAGGTTATCAAAAGC	7110
rs776713357	snp	C/T	1.68687e-05	0.00290414	intron-variant	TMF1	GRCh38.p7	3:69033745	TACCAATGACAGCAA[C/T]AAAAACATTAAAAAC	7110
rs776737178	snp	A/G	1.71947e-05	0.00293207	intron-variant	TMF1	GRCh38.p7	3:69044623	AATACATAAAAGTCA[A/G]AACGCTTAGCTTTAA	7110
rs776780126	snp	A/T			intron-variant	TMF1	GRCh38.p7	3:69040286	GGGCAGAACAAATGA[A/T]CAATTATAACAGACA	7110
rs776782051	snp	A/T			synonymous-codon	TMF1	GRCh38.p7	3:69047955	GGTAGAAGTACCTGA[A/T]GAAAAGGTACTAACA	7110
rs776807922	snp	A/G	1.66181e-05	0.00288249	missense	TMF1	GRCh38.p7	3:69048073	TGCGTAGACGTATTA[A/G]ATATACTTTCCATAG	7110
rs776865818	snp	A/C	1.6571e-05	0.0028784	synonymous-codon	TMF1	GRCh38.p7	3:69048162	ATCCGATTCTTTATT[A/C]ACAGTTTCTTCGTGC	7110
rs776867549	snp	C/G	1.65693e-05	0.00287826	missense	TMF1	GRCh38.p7	3:69042847	CTCATCTTTCTCTTT[C/G]AAAAGGTCTGCAGTT	7110
rs776879235	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69034708	CAGAGGCATAGAAAC[C/T]GGGAACTATTACCTG	7110
rs776947132	snp	C/T			intron-variant, downstream-variant-500B	TMF1, MIR3136	GRCh38.p7	3:69048819	TGGGCCTGGCCTGGA[C/T]TACCAGATGCGAGTA	7110
rs776976891	snp	A/G	1.70417e-05	0.002919	missense	TMF1	GRCh38.p7	3:69029833	TTGTTCTCATCCTCC[A/G]GTTTACACAGCCTAT	7110
rs776993883	snp	A/C			missense	TMF1	GRCh38.p7	3:69024090	TGGGTATCTCCTTCA[A/C]CTTCTCTTCAAGTTC	7110
rs777000112	snp	C/T	1.65685e-05	0.00287819	missense	TMF1	GRCh38.p7	3:69047669	TGCCTGACAATTCAT[C/T]ATCTGAATTGATTTC	7110
rs777012513	snp	A/C	1.69218e-05	0.00290871	intron-variant	TMF1	GRCh38.p7	3:69026135	GTTCATATTAAAGAG[A/C]AAAGAGATAAGCAGA	7110
rs777052010	snp	A/G	4.97335e-05	0.00498641	synonymous-codon	TMF1	GRCh38.p7	3:69026004	ACATCACCTGAGACA[A/G]AAAAGATGTCTGTAG	7110
rs777130370	in-del	-/A	1.6549e-05	0.0028765	intron-variant	TMF1	GRCh38.p7	3:69028185	CCCCAACCATTCTCT[-/A]ATGTATGCCCTAAGA	7110
rs777148689	in-del	-/AT	3.39331e-05	0.00411891	intron-variant	TMF1	GRCh38.p7	3:69024218	AGTTTAAATCAAAAC[-/AT]ATCTTTTTTAATACT	7110
rs777149507	snp	G/T			intron-variant	TMF1	GRCh38.p7	3:69043631	CAATTTAAATGTTAA[G/T]AGATGATATCCTTTT	7110
rs777181784	in-del	-/AC			intron-variant	TMF1	GRCh38.p7	3:69031419	TTTAGAACTTAATAC[-/AC]ACACACACACACACA	7110
rs777243466	snp	C/T	1.65745e-05	0.00287871	intron-variant	TMF1	GRCh38.p7	3:69035136	GGAGGAGAAACAATA[C/T]ATTCACAAACAATGG	7110
rs777261366	snp	C/T	4.99471e-05	0.00499711	synonymous-codon	TMF1	GRCh38.p7	3:69051958	ACCCGGCTCTCCATA[C/T]GGAATGGTCTCGGCC	7110
rs777273848	snp	G/T	1.65916e-05	0.00288019	missense	TMF1	GRCh38.p7	3:69047759	CAGATGAACAGCAAC[G/T]CTCAGTGAGTTTTTG	7110
rs777276833	snp	G/T	1.65677e-05	0.00287812	intron-variant	TMF1	GRCh38.p7	3:69035121	GGTCCCCCACCTGTA[G/T]GAGGAGAAACAATAC	7110
rs777277643	snp	A/C/T	3.37942e-05	0.0041105	missense	TMF1	GRCh38.p7	3:69052083	AGGCGTTGAACCAAC[A/C/T]CATCGCCCCTCCTCA	7110
rs777352221	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69032562	TTTCTTTTTATTAAC[A/G]TCACAGAAGGGCAAC	7110
rs777385319	in-del	-/A			intron-variant	TMF1	GRCh38.p7	3:69024660	GATCTACTTTTTGCC[-/A]ATTCAAGTTCTTTAA	7110
rs777446364	snp	A/C			intron-variant	TMF1	GRCh38.p7	3:69041611	ACATATTATGGTATA[A/C]CCATATAATGGACTT	7110
rs777447126	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69030789	AGGGACGACATAAAA[C/T]GTTGGCAAGGGTGTG	7110
rs777559163	snp	C/G			utr-variant-3-prime	TMF1	GRCh38.p7	3:69022915	GATAAAGTAATAAAT[C/G]TCTGTGCTATTCAAG	7110
rs777562709	snp	A/C	1.66679e-05	0.00288681	missense	TMF1	GRCh38.p7	3:69047855	TCAAGTGAAGACTTG[A/C]TTTTGAATCTGTAGT	7110
rs777608536	snp	A/T	1.67158e-05	0.00289096	intron-variant	TMF1	GRCh38.p7	3:69026113	CTTAGGGAGTAAAAA[A/T]AATTCTGTTCATATT	7110
rs777661595	snp	A/C	4.96808e-05	0.00498377	missense	TMF1	GRCh38.p7	3:69048416	AGAGAAAGGCACTGA[A/C]GAAATTTTCAGATTC	7110
rs777673026	snp	C/T	3.4727e-05	0.00416681	missense	TMF1	GRCh38.p7	3:69029818	AACCATGCTCACCTA[C/T]TGTTCTCATCCTCCA	7110
rs777731676	snp	C/T	1.65743e-05	0.00287869	missense	TMF1	GRCh38.p7	3:69039634	CATTCTCCTTGTCTT[C/T]AGCTCTTAATTTCTT	7110
rs777732774	snp	G/T			intron-variant	TMF1	GRCh38.p7	3:69043182	TTTCATTTTTATTTT[G/T]ATTTTTTGAGACAGG	7110
rs777813714	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69025408	CTCTTTTTAGCCTTT[A/G]TCATTGATATATGTG	7110
rs777859397	in-del	-/TG			upstream-variant-2KB	TMF1	GRCh38.p7	3:69052730	ATCACGTATGAACAC[-/TG]TGTCCAACTCGTGGA	7110
rs777862218	in-del	-/TTAT			intron-variant	TMF1	GRCh38.p7	3:69024418	CAGAGATAAATCCAA[-/TTAT]TTATTTGTTTGAAAA	7110
rs777921802	snp	A/G	3.31549e-05	0.0040714	synonymous-codon	TMF1	GRCh38.p7	3:69029919	ATTCTGTGACTCCAT[A/G]GAAGACATCTGAATT	7110
rs777930892	snp	G/T	1.69951e-05	0.00291501	missense	TMF1	GRCh38.p7	3:69043873	TTTCACTCTGAACAT[G/T]TCACTAAATTTAAAA	7110
rs777974167	snp	A/T	5.85543e-05	0.00541052	missense	TMF1	GRCh38.p7	3:69023317	TGTACCTTTGATCCA[A/T]ATCCTGAAAAATGTA	7110
rs778032733	snp	A/G			missense	TMF1	GRCh38.p7	3:69048262	TTTACTTGTGATTCA[A/G]TTGTTTCAGGAGTTC	7110
rs778132977	snp	A/G	1.65616e-05	0.00287759	synonymous-codon	TMF1	GRCh38.p7	3:69047490	GATATCAGGCTGTTC[A/G]CAGTTAACAGGAGTT	7110
rs778222258	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69040703	GAAGCAGGCGGATCA[C/T]CAGAGGTCAGGAGTT	7110
rs778270542	snp	C/G	1.65608e-05	0.00287752	missense	TMF1	GRCh38.p7	3:69048254	AAGAGTCTTTTACTT[C/G]TGATTCAGTTGTTTC	7110
rs778293404	snp	C/T	3.31329e-05	0.00407005	missense	TMF1	GRCh38.p7	3:69026070	GTGACATGGTGGGAG[C/T]GCTAGAAACAGAAAA	7110
rs778345911	snp	A/C/T	4.98561e-05	0.00499259	synonymous-codon, missense	TMF1	GRCh38.p7	3:69052024	CCTGTCAATAGACTT[A/C/T]TGGGCCTGGGACAGG	7110
rs778439124	snp	A/G	1.72166e-05	0.00293394	intron-variant	TMF1	GRCh38.p7	3:69025957	ATTTCCTTTATTATT[A/G]TTCTAAGAACTAAGC	7110
rs778519079	snp	G/T	1.65625e-05	0.00287766	missense	TMF1	GRCh38.p7	3:69035107	CAATGCAAGCCTAAG[G/T]TCCCCCACCTGTAGG	7110
rs778598307	snp	C/T			upstream-variant-2KB	TMF1	GRCh38.p7	3:69053284	GGTGGCCTTCCTAAT[C/T]CAGTCTGCAGCTATA	7110
rs778614786	snp	A/G			downstream-variant-500B	TMF1	GRCh38.p7	3:69019509	ATACAAAAATTAGCC[A/G]GATGTGCTGGTGCGC	7110
rs778696865	snp	A/G	1.97556e-05	0.00314284	intron-variant	TMF1	GRCh38.p7	3:69042947	TGAATACCGTAAAGA[A/G]TGACTTTCACTCTAA	7110
rs778731112	snp	G/T	4.18778e-05	0.00457571			GRCh38.p7	3:69039060	AGAAATAATACCATG[G/T]TAAATAACTGTATTC	7110
rs778765748	snp	C/T	1.66078e-05	0.00288161	missense	TMF1	GRCh38.p7	3:69038931	GGCCAAGATCTTTCT[C/T]TTGGCGTTCTACCAT	7110
rs778791803	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69046062	CCCTGTGAGCCGCGA[C/T]CGCACCACTGCACGC	7110
rs778822791	snp	C/T	1.65924e-05	0.00288027	synonymous-codon	TMF1	GRCh38.p7	3:69038720	AAGATCAGTAAGTTC[C/T]CTTAAAAAATTAGAT	7110
rs778873295	snp	A/G	1.65875e-05	0.00287984	synonymous-codon	TMF1	GRCh38.p7	3:69047751	AAAAGCATCAGATGA[A/G]CAGCAACTCTCAGTG	7110
rs778905433	snp	G/T			intron-variant	TMF1	GRCh38.p7	3:69025017	TGACTGCATAAAGTT[G/T]TTTAAAAGCCAAAAA	7110
rs778977831	snp	C/T	5.04206e-05	0.00502073	missense	TMF1	GRCh38.p7	3:69028258	CTTCAAGTGTTCTTA[C/T]ATATTCATCTTTTAG	7110
rs779015389	snp	A/G	1.65622e-05	0.00287764	missense	TMF1	GRCh38.p7	3:69047465	CATTTATTGGTGTGG[A/G]AGAAACCAAGATATC	7110
rs779036305	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69044907	TAGGTATACCTTAGA[A/G]GAGAAAATTCTTGCA	7110
rs779066237	in-del	-/T			utr-variant-5-prime	TMF1	GRCh38.p7	3:69052307	GCATGCGCTTGCTTC[-/T]TCCACGTACACAGCA	7110
rs779066515	snp	A/G	0.000151168	0.00869258	intron-variant	TMF1	GRCh38.p7	3:69038807	CTACTCTGATAATTC[A/G]TTCTAAATGGGTTGC	7110
rs779070346	snp	A/T	1.65726e-05	0.00287855	missense	TMF1	GRCh38.p7	3:69025616	ACTGTAGGTTTTCAA[A/T]TATGCTTGATCCTGC	7110
rs779082423	snp	A/G	1.6585e-05	0.00287962	missense	TMF1	GRCh38.p7	3:69048136	TTCAAACTTACAGTT[A/G]GCACCTTCATATCCG	7110
rs779084468	snp	C/G			intron-variant	TMF1	GRCh38.p7	3:69030284	GTCCTGGAGCAACTG[C/G]ACAGCTATATGCAAA	7110
rs779151780	in-del	-/G	2.03793e-05	0.00319205	frameshift-variant	TMF1	GRCh38.p7	3:69027975	CTTTCCATTTCTAAC[-/G]TGACTATTCAACAAT	7110
rs779253956	snp	A/G	1.78341e-05	0.00298609	utr-variant-3-prime	TMF1	GRCh38.p7	3:69023160	ATTCAGTTTGATGGG[A/G]ATTCAATTTTCACAA	7110
rs779264823	snp	A/G			intron-variant, upstream-variant-2KB	TMF1, MIR3136	GRCh38.p7	3:69049455	CATATTAAACTGATG[A/G]GAATGGTAAGTTCTA	7110
rs779361749	snp	A/C			intron-variant	TMF1	GRCh38.p7	3:69028981	CCACACAATCTCAAC[A/C]ATCTACATGACAATG	7110
rs779445426	snp	A/C	1.65655e-05	0.00287793	splice-donor-variant	TMF1	GRCh38.p7	3:69035022	AAACCTGTGACAGTA[A/C]CTGCTGAAGTTCACC	7110
rs779464362	snp	C/T	1.7912e-05	0.0029926	intron-variant	TMF1	GRCh38.p7	3:69029775	AGTGCTTTAGGATGT[C/T]ACGGAACTACCAAAA	7110
rs779497960	snp	C/T	1.66394e-05	0.00288434	synonymous-codon	TMF1	GRCh38.p7	3:69048048	GTCCTTTGTTTCTGC[C/T]GTGAGAGACTGCGTA	7110
rs779552233	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69038204	TTGTTTTTCCTACTT[C/T]ATCTGAGGTCCTTGG	7110
rs779573685	snp	A/T	1.65949e-05	0.00288048	missense	TMF1	GRCh38.p7	3:69033694	TTTCGATTCTCTGCT[A/T]CCTGGAGTCTCTGAA	7110
rs779626431	snp	C/T	1.6571e-05	0.0028784	missense	TMF1	GRCh38.p7	3:69025646	CTCCCATCCTTACAG[C/T]ATCATAAAGATTGCT	7110
rs779631430	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69040815	TAGTCTCAGCTATTC[A/G]GGAGGCTGAGGCAGG	7110
rs779671834	snp	C/T	1.85941e-05	0.00304905	intron-variant	TMF1	GRCh38.p7	3:69042929	TAATAAAAAAGAAAT[C/T]TGTGAATACCGTAAA	7110
rs779727514	snp	G/T			intron-variant	TMF1	GRCh38.p7	3:69042072	GACAAAGTCTCACTC[G/T]GTCGCCCAGGCTGCA	7110
rs779806673	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69028048	AATTCATGCCATGAT[A/G]AGTCAATCTCAAAGT	7110
rs779831523	snp	C/G	4.96989e-05	0.00498467	missense	TMF1	GRCh38.p7	3:69047620	GACTTTGGAGTTGAA[C/G]AATTAACTATAATAG	7110
rs779847595	snp	A/C/T	3.33052e-05	0.00408065	missense	TMF1	GRCh38.p7	3:69048032	TAGGTTCCAAAGCTA[A/C/T]GTCCTTTGTTTCTGC	7110
rs779852692	snp	A/G	9.26856e-05	0.00680692	intron-variant, downstream-variant-500B	TMF1, MIR3136	GRCh38.p7	3:69048612	ATATATGTTACATTA[A/G]TATTTCAATCATCAT	7110
rs779878755	snp	C/T	4.96899e-05	0.00498422	missense	TMF1	GRCh38.p7	3:69026039	GCCATATCAACACCA[C/T]TTATTGAACTTGAGC	7110
rs779900492	snp	A/C	1.66219e-05	0.00288283	intron-variant	TMF1	GRCh38.p7	3:69042784	TACAGTATTTTTCAT[A/C]GTCAACCAAATACTA	7110
rs779902483	snp	G/T	1.6593e-05	0.00288031	missense	TMF1	GRCh38.p7	3:69048110	TCACATCAATTACAC[G/T]TTCAGATACTTTCAA	7110
rs779930297	in-del	-/TCTG	0.000169305	0.00919912	intron-variant	TMF1	GRCh38.p7	3:69042563	AGGGCAGCACAAATT[-/TCTG]TCTATTTTACAGGGA	7110
rs779967198	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69035486	ACTCATATGCAGGAG[C/T]ATACATTATAAACTA	7110
rs779981737	snp	A/G	1.66048e-05	0.00288134	synonymous-codon	TMF1	GRCh38.p7	3:69052006	TTCCTGGATGTCCAG[A/G]ACCCTGTCAATAGAC	7110
rs780112508	snp	A/G			synonymous-codon	TMF1	GRCh38.p7	3:69025607	TTAGCTGAGACTGTA[A/G]GTTTTCAATTATGCT	7110
rs780141154	snp	A/G	1.65679e-05	0.00287814	missense, downstream-variant-500B	TMF1, MIR3136	GRCh38.p7	3:69048487	GGAGAGGCTATTGGT[A/G]GACTCTGAGGTTCAG	7110
rs780153809	snp	C/T	1.65603e-05	0.00287747	synonymous-codon	TMF1	GRCh38.p7	3:69048396	GGTCTGGACATCAGT[C/T]GGCGAGAGAAAGGCA	7110
rs780181091	snp	A/G			downstream-variant-500B	TMF1	GRCh38.p7	3:69019451	AGGTCACTTGAGTTC[A/G]AAACCAGCCTGGCCA	7110
rs780208741	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69039423	TCTTATCATTTATCT[A/G]TTGTTTGAAAAATCC	7110
rs780260921	snp	C/G/T	3.31957e-05	0.00407394	missense	TMF1	GRCh38.p7	3:69024168	GAGTTTTTTCTAGAT[C/G/T]GCCAATTTCTAGCTG	7110
rs780405293	snp	C/T	3.58667e-05	0.00423463	intron-variant	TMF1	GRCh38.p7	3:69029765	ACTTTTAAAAAGTGC[C/T]TTAGGATGTCACGGA	7110
rs780580921	snp	C/T	1.65649e-05	0.00287788	missense	TMF1	GRCh38.p7	3:69038683	CCTGTGCCTCACTAT[C/T]CTTTGCAGCATTGGC	7110
rs780593239	snp	A/C			intron-variant, upstream-variant-2KB	TMF1, MIR3136	GRCh38.p7	3:69050803	AAAATTAAGAACAGA[A/C]ACCAGAAAGGAGTAG	7110
rs780597222	snp	A/G	1.80549e-05	0.00300452	intron-variant	TMF1	GRCh38.p7	3:69047343	CTAAAAATCCCTTCC[A/G]CTTACTAGAGTTACC	7110
rs780610373	snp	A/T			intron-variant	TMF1	GRCh38.p7	3:69032021	TTTATACCTATAAAT[A/T]TAAATATATATGAAG	7110
rs780682771	snp	C/G	1.66554e-05	0.00288573	intron-variant	TMF1	GRCh38.p7	3:69039699	AGTTTTTCTCCTGGT[C/G]ATGGTAAAGAAGTAT	7110
rs780773073	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69038302	ATGTGCATTTTTGCT[C/T]TTCTCTTCTAAGAGG	7110
rs780786282	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69042741	AGGAAGCATCAGCTA[A/G]TTATGTGGCAAGTAC	7110
rs780970902	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69036758	AGTTTTCTCAACAAC[C/T]GGTCCTGCAACAACT	7110
rs780984515	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69030688	ATAAAATGATGTTCA[A/G]TAACATTAGCCATTA	7110
rs780995516	snp	C/T	2.50888e-05	0.00354172	intron-variant, downstream-variant-500B	TMF1, MIR3136	GRCh38.p7	3:69048598	TTAAAAAAGAACACA[C/T]ATATGTTACATTAAT	7110
rs781001108	snp	A/G	3.31669e-05	0.00407215	synonymous-codon, downstream-variant-500B	TMF1, MIR3136	GRCh38.p7	3:69048501	TGGACTCTGAGGTTC[A/G]GTGTTTGATTTCAAC	7110
rs781080832	snp	C/T	0.000105406	0.0072589	missense	TMF1	GRCh38.p7	3:69023188	CAAGTTAACTGAGAC[C/T]TTGTCTTAAAAGTTC	7110
rs781090049	snp	A/G			utr-variant-3-prime	TMF1	GRCh38.p7	3:69021280	GTCTATACTATCCAT[A/G]GTTTCAGACGTTCAC	7110
rs781093992	snp	C/T	3.31549e-05	0.0040714	missense	TMF1	GRCh38.p7	3:69033581	TCTTCTCTAATTTCT[C/T]CCACGACGATGTCTG	7110
rs781243067	snp	C/T			synonymous-codon	TMF1	GRCh38.p7	3:69047982	AACAGGAGGAGAAGG[C/T]GTATTGCTCTGCCTG	7110
rs781368004	snp	C/T	1.65737e-05	0.00287864	synonymous-codon	TMF1	GRCh38.p7	3:69038582	AATGGCTAATGTTTC[C/T]TGCTGCTGACGGGCT	7110
rs781368738	snp	C/G	1.70067e-05	0.002916	intron-variant	TMF1	GRCh38.p7	3:69030018	TTCACCTGATTACAG[C/G]ACAGAAAAAAAAATC	7110
rs781381447	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69026920	TTAAATTTACCTATC[A/G]GTAGTTTAAATATAT	7110
rs781421230	snp	C/T	4.07577e-05	0.00451411	synonymous-codon	TMF1	GRCh38.p7	3:69027975	TCTTTCCATTTCTAA[C/T]TGACTATTCAACAAT	7110
rs781430005	snp	A/C	2.16908e-05	0.00329316	intron-variant	TMF1	GRCh38.p7	3:69023342	AATGTATTTGTTTAC[A/C]ATTTTTAAAATAACT	7110
rs781454444	in-del	-/A	0.000258152	0.0113582	intron-variant, downstream-variant-500B	TMF1, MIR3136	GRCh38.p7	3:69048578	CTTTAACAAAAAAGT[-/A]AATATTAAAAAAGAA	7110
rs781530618	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69046379	AAATTCAAAAATATC[C/T]GATAGTAATTAGTGC	7110
rs781550450	snp	C/T	1.65987e-05	0.00288082	missense	TMF1	GRCh38.p7	3:69038925	GAAGACGGCCAAGAT[C/T]TTTCTCTTGGCGTTC	7110
rs781643362	snp	G/T	0.000364275	0.0134909	missense	TMF1	GRCh38.p7	3:69048380	CTGGACTCTTCTGAA[G/T]GGTCTGGACATCAGT	7110
rs781659534	snp	A/G	1.72973e-05	0.00294081	intron-variant	TMF1	GRCh38.p7	3:69043903	ATAATATTTGAGAAT[A/G]AGGATGGTGTCTATA	7110
rs781700955	in-del	-/AT			upstream-variant-2KB	TMF1	GRCh38.p7	3:69054087	AAGTAACCAAAAAAC[-/AT]TTGAACAGAAAACTG	7110
rs781775711	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69033110	AGTGCAGCAGTCTAC[C/T]AAAAATACAAAAAAT	7110
rs781777146	in-del	-/AAT	3.42144e-05	0.00413594	intron-variant	TMF1	GRCh38.p7	3:69043887	TTTCACTAAATTTAA[-/AAT]AATATTTGAGAATGA	7110
rs796098683	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69045872	CAAGACCAGCCTGGC[A/G]GCATAGTGAGACCTC	7110
rs796169371	snp	G/T			intron-variant	TMF1	GRCh38.p7	3:69044663	TTTTTACATGCAGGT[G/T]TATCACTGTAACAAA	7110
rs796195640	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69033016	AGTGATGAGAATCAT[A/G]TATGATCTCTACCTC	7110
rs796239797	snp	G/T			intron-variant	TMF1	GRCh38.p7	3:69045071	TAAAGCCTCTATATT[G/T]TAGCTAGGTGGTGGA	7110
rs796246651	in-del	-/G			downstream-variant-500B, upstream-variant-2KB	UBA3, TMF1	GRCh38.p7	3:69054290	GAAGCCGAGGGGGGC[-/G]GGGGGGGGGTGGATC	7110
rs796339940	snp	A/C			intron-variant	TMF1	GRCh38.p7	3:69025427	TTGATATATGTGATA[A/C]ATTTTGGGCTTCACA	7110
rs796361589	in-del	-/AC			intron-variant	TMF1	GRCh38.p7	3:69031418	TGTTTAGAACTTAAT[-/AC]ACACACACACACACA	7110
rs796525596	snp	A/T			intron-variant	TMF1	GRCh38.p7	3:69039997	AGTTTTGGCATCACC[A/T]ATTGTAGTACAGCCT	7110
rs796656895	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69037471	ATGGTGAAGCCTCGT[C/T]TCTACTAAAAAAAAA	7110
rs796756715	snp	A/G			upstream-variant-2KB	TMF1	GRCh38.p7	3:69053885	TCACCTTCTTACAAT[A/G]CTACTTTGAGAATTA	7110
rs796820903	snp	A/G			intron-variant, upstream-variant-2KB	TMF1, MIR3136	GRCh38.p7	3:69050666	ATATGAAAAAACAGA[A/G]TTACTCCAGCAAGGT	7110
rs796823115	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69032178	CCAGCCTCTTATTTA[C/T]CAAGCTTCCCTCTCA	7110
rs796860322	snp	A/G			intron-variant	TMF1	GRCh38.p7	3:69031645	AAAATTTTCAATTGA[A/G]AAAAAGAGCAATGGG	7110
rs796910431	in-del	-/A			intron-variant	TMF1	GRCh38.p7	3:69037477	AGCCTCGTCTCTACT[-/A]AAAAAAAAACAAAAA	7110
rs796977082	snp	C/T			intron-variant	TMF1	GRCh38.p7	3:69025891	AAGTATTCAGATGAA[C/T]TACCCATAGAATGGC	7110

Page 1 | 2