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

TFG

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs7297	snp	A/T	0.459347	0.136653	utr-variant-3-prime	TFG	GRCh38.p7	3:100748832	GGCTAAACCTCACCC[A/T]AGCATTTTAATATCC	10342
rs11353	snp	C/T	0.42058	0.182764	synonymous-codon	TFG	GRCh38.p7	3:100748174	TCAGCAGACTGGACC[C/T]CAACAACCTCAGCAG	10342
rs12128	snp	C/T	0	0	utr-variant-3-prime, downstream-variant-500B	TFG, ABI3BP	GRCh38.p7	3:100748901	ATAATATCTTGTATT[C/T]TCAAAGGGCTCTACT	10342
rs12562	snp	G/T	0.0095275	0.0683592	synonymous-codon	TFG	GRCh38.p7	3:100736589	AGGGCCACCCAGTGC[G/T]CCTGCAGAAGATCGT	10342
rs186920	snp	A/G	0	0	intron-variant	TFG	GRCh38.p7	3:100732261	ATGTTTCTTACAAAA[A/G]GAGGTAAATAATTTT	10342
rs186956	snp	C/G	0	0	intron-variant	TFG	GRCh38.p7	3:100740715	ATTATTTATTACACA[C/G]AGTAGCCAACCTCTA	10342
rs193210	snp	A/C	0	0	intron-variant	TFG	GRCh38.p7	3:100736733	TAAAATAGAGTTTAG[A/C]ACACATGTTTGGGAA	10342
rs368423	snp	A/G	0	0	intron-variant	TFG	GRCh38.p7	3:100720434	gcgactactgGTTTC[A/G]AGTATCAGACTTACA	10342
rs392104	snp	A/C			intron-variant	TFG	GRCh38.p7	3:100723100	GCATTGATTGTGACA[A/C]AATTAATAGTCTTAT	10342
rs395000	snp	G/T	0	0	intron-variant	TFG	GRCh38.p7	3:100735750	CATTCATTTCTGTGT[G/T]CATTATTTTGTAAGA	10342
rs397320	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100732195	GCTCCAAAAAAACCC[A/G]AAAAAGTAAAATGTT	10342
rs407114	snp	A/C			intron-variant	TFG	GRCh38.p7	3:100723138	AAACAATTTGGGACA[A/C]AAATACTGGGCAATA	10342
rs420281	snp	C/G	0	0	intron-variant	TFG	GRCh38.p7	3:100722928	GAAGCAATGTGAGCA[C/G]ATAAACTGTTGCTTG	10342
rs420630	snp	C/G			intron-variant	TFG	GRCh38.p7	3:100722377	aagcacacaaacaCA[C/G]GCGAAAGAGAAGTTG	10342
rs421275	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100722470	AAATACATTGAGGTA[A/G]TGACTAAAGAAATTT	10342
rs421344	snp	C/G			intron-variant	TFG	GRCh38.p7	3:100720509	ctatggaagggggca[C/G]gagaaggtttgggga	10342
rs422081	snp	A/C			intron-variant	TFG	GRCh38.p7	3:100723128	TATGGAATAAAAACA[A/C]TTTGGGACACAAATA	10342
rs423966	snp	G/T			intron-variant	TFG	GRCh38.p7	3:100720474	tgcactggaaactgg[G/T]ttcgtgtaagacagt	10342
rs424381	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100732254	TTTACCTCCTTTTGT[A/G]AGAAACATTAGATGA	10342
rs427906	snp	C/G			intron-variant	TFG	GRCh38.p7	3:100722357	tccaaagaaattaca[C/G]agtaaagcacaaaaa	10342
rs430945	snp	A/G	0.244417	0.252512	missense	TFG	GRCh38.p7	3:100736627	GCTGAGGAGGAGGAA[A/G]CAATGCTGTGGGGTG	10342
rs435035	snp	A/C			intron-variant	TFG	GRCh38.p7	3:100732228	GATGAAAAAAATACA[A/C]GCTCCTTGATAAAGA	10342
rs447236	snp	C/G			intron-variant	TFG	GRCh38.p7	3:100735290	TCTGATGTATCCCCA[C/G]AACTTACCACAGTAT	10342
rs448493	snp	G/T			intron-variant	TFG	GRCh38.p7	3:100723096	ATGAGCATTGATTGT[G/T]ACAAAATTAATAGTC	10342
rs448919	snp	A/C	0	0	intron-variant	TFG	GRCh38.p7	3:100732289	AACAGAAGATGAACA[A/C]AAGCTTTCCAAAAAA	10342
rs453716	snp	C/T	0	0	intron-variant	TFG	GRCh38.p7	3:100735355	TGCCATATAAGTACT[C/T]GCTATTATCAGCAGA	10342
rs497835	snp	G/T	0	0	intron-variant	TFG	GRCh38.p7	3:100737494	CTGGAAGGCACCCTA[G/T]AGATTAGTTAAGTAC	10342
rs571403	snp	A/C			downstream-variant-500B	TFG, ABI3BP	GRCh38.p7	3:100749037	AAGACCACCACACCA[A/C]TAAGGACTTCTGAAA	10342
rs571521	snp	G/T			downstream-variant-500B	TFG, ABI3BP	GRCh38.p7	3:100748996	TTTTTCACATAATGT[G/T]AGTGACTAAATTAAA	10342
rs572352	snp	A/T	0	0	utr-variant-3-prime, downstream-variant-500B	TFG, ABI3BP	GRCh38.p7	3:100748931	TTAACCTATCATCAG[A/T]GTTACATTTTATACA	10342
rs573376	snp	G/T			utr-variant-3-prime	TFG	GRCh38.p7	3:100748798	GGACAAGGGAAGCTA[G/T]AAAGTCAAGTCAATC	10342
rs574795	snp	A/T			intron-variant	TFG	GRCh38.p7	3:100718542	aaaaaaaCCCTTGAA[A/T]TACAAAGTTGTAACT	10342
rs591728	snp	A/G	0.239614	0.249784	intron-variant	TFG	GRCh38.p7	3:100714748	ACTCCTACAATAAAG[A/G]AACACTTTTGTCTTT	10342
rs628268	snp	A/C/G/T	0	0	utr-variant-3-prime	TFG	GRCh38.p7	3:100748830	GAGGATATTAAAATG[A/C/G/T]TAGGGTGAGGTTTAG	10342
rs664333	snp	A/T	0.101403	0.201045	intron-variant	TFG	GRCh38.p7	3:100736422	TGGAGCAAAGGAAAA[A/T]ATAAAGTACATACAT	10342
rs665230	snp	G/T	0	0	missense	TFG	GRCh38.p7	3:100736624	GAACACCCGACAGCA[G/T]TGCTTCCTCCTCCTC	10342
rs931206	snp	A/G	0.427575	0.175975	intron-variant	TFG	GRCh38.p7	3:100735434	TTATAAGCCCATGCT[A/G]TAAGCTCTTGTAAAC	10342
rs967308	snp	C/T	0.0577344	0.159793	upstream-variant-2KB	TFG	GRCh38.p7	3:100708832	TTGGCTATAAATTCC[C/T]ACTTACTCATACTGT	10342
rs967309	snp	C/T	0.0577344	0.159793	upstream-variant-2KB	TFG	GRCh38.p7	3:100708894	AGAGTACGTAGGACA[C/T]ACTCAAATGCCTTAT	10342
rs1012364	snp	A/T	0.420733	0.18262	intron-variant	TFG	GRCh38.p7	3:100734067	agtttttttttttgc[A/T]tttttttttgcaaag	10342
rs1015198	snp	A/C			intron-variant	TFG	GRCh38.p7	3:100734560	AAACCAGAGGAGTTT[A/C]CCCCAATAAAATTAG	10342
rs1055213	snp	A/G	0.19459	0.243782	intron-variant	TFG	GRCh38.p7	3:100746432	TGCAGAATGATACAG[A/G]GAAATACTGAACTGA	10342
rs1059363	snp	C/G	0.409041	0.192888	intron-variant, utr-variant-5-prime, upstream-variant-2KB	TFG	GRCh38.p7	3:100709616	CGAAGGGCAACCGAG[C/G]GGGCCGTGACCACCG	10342
rs1059503	snp	A/G	0.123105	0.215401	utr-variant-3-prime	TFG	GRCh38.p7	3:100748829	GGAGGATATTAAAAT[A/G]CTAGGGTGAGGTTTA	10342
rs1065628	snp	A/C/T	1.6504e-05	0.00287258	missense	TFG	GRCh38.p7	3:100713729	AGCTAATCATCAAAG[A/C/T]TCAACTTGGGGAGGA	10342
rs1133721	snp	A/T			intron-variant	TFG	GRCh38.p7	3:100746301	cccagagattttgaa[A/T]ttcatttgattgggt	10342
rs1143775	snp	A/T	0.295088	0.245901	intron-variant	TFG	GRCh38.p7	3:100728572	AGTAACTTTTTTTTT[A/T]AAAAAAAAGAATTCT	10342
rs1143776	snp	A/G	0.227369	0.248974	upstream-variant-2KB	TFG	GRCh38.p7	3:100709274	AATACCCGCTTTCGA[A/G]AAAACCGGAAGTGCG	10342
rs1143777	snp	A/T	0.127599	0.217986	upstream-variant-2KB	TFG	GRCh38.p7	3:100708090	agaaggactccatac[A/T]tctatacttgaatcc	10342
rs1144104	snp	G/T	0.251578	0.249995	intron-variant	TFG	GRCh38.p7	3:100729339	ATGGTATGTTGTAAA[G/T]TTGAAACACAGTTTT	10342
rs1144105	snp	C/T	0.228547	0.249078	intron-variant	TFG	GRCh38.p7	3:100724075	AAAAACTTGGTTACA[C/T]AGAAGTCATTATCTA	10342
rs1144106	snp	C/T	0.241627	0.24986	intron-variant	TFG	GRCh38.p7	3:100723542	TCTTTTCCTAGCCCT[C/T]TACTTTCAAGCTTTG	10342
rs1144107	snp	C/T	0.240478	0.249819	intron-variant	TFG	GRCh38.p7	3:100722872	TAACAGTGGTCTTCA[C/T]CAAGAAGGAAATTTA	10342
rs1384198	snp	C/G	0.409212	0.192748	intron-variant	TFG	GRCh38.p7	3:100729920	TCTGAAATAGAAGTG[C/G]AACTAGGAATAATCA	10342
rs1402252	snp	C/G	0.459347	0.136653	intron-variant	TFG	GRCh38.p7	3:100729644	TTTCATAGTTTAAAA[C/G]TGTCCATATTGTGAA	10342
rs1503838	snp	A/G	0.446972	0.153955	intron-variant	TFG	GRCh38.p7	3:100719940	CTGAAAATTTAAAAA[A/G]TTAAAAAACAACCTT	10342
rs1520649	snp	C/T	0.427575	0.175975	intron-variant	TFG	GRCh38.p7	3:100723634	TTCTTTTTATCATCA[C/T]AAAGTGACTATTACT	10342
rs1628175	snp	C/G			intron-variant	TFG	GRCh38.p7	3:100729399	ACAAACAGTACATGT[C/G]ATTATACAATGGGGA	10342
rs1718279	snp	A/C	0.228547	0.249078	intron-variant	TFG	GRCh38.p7	3:100741122	aatatagtatagtaa[A/C]ttcacaaatgagtaa	10342
rs1809962	snp	C/G			intron-variant	TFG	GRCh38.p7	3:100734973	CCCTCCTTCCCACTG[C/G]CACATTCATTATTCT	10342
rs1812160	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100735285	GCATAATACTGTGGT[A/G]AGTTGTGGGGACACA	10342
rs1903744	snp	C/T	0.459347	0.136653	intron-variant	TFG	GRCh38.p7	3:100728321	GAGCTTTTTAAGTTA[C/T]ATAATTTTTATTAAA	10342
rs1915309	snp	A/G	0.434253	0.168969	intron-variant	TFG	GRCh38.p7	3:100716575	atcgaactaacacac[A/G]attcagcgatgccac	10342
rs2126540	snp	A/C	0.409212	0.192748	intron-variant	TFG	GRCh38.p7	3:100743683	CTACCCAGCACTAAA[A/C]ACTTAGACACGTATA	10342
rs2126541	snp	A/C	0.41023	0.191902	downstream-variant-500B	TFG, ABI3BP	GRCh38.p7	3:100749273	AGTGATTTTCCTTCT[A/C]GATAAAAGGTATAGT	10342
rs2139691	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100724589	TGAATTAGTGTATAT[C/T]CCCTCTTTGCCTATG	10342
rs2272082	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100736550	AAAAAAAAGTCAGTT[C/T]AGTATCCAACACAAG	10342
rs2293030	snp	G/T	0.427879	0.175668	intron-variant	TFG	GRCh38.p7	3:100744424	CTTCCTAAAGCACTG[G/T]ATTTGCCCTCTAAAG	10342
rs2316942	snp	A/T			intron-variant	TFG	GRCh38.p7	3:100728368	aaatttaataaatat[A/T]taaGAACAGCATGAA	10342
rs2447456	snp	A/G	0.251578	0.249995	intron-variant	TFG	GRCh38.p7	3:100715498	AACTTATACTGTGGA[A/G]GAGAAGTGTAAATCA	10342
rs2449252	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100718516	TAACTAATTGGGGAA[A/G]ACAAACTACAACGAG	10342
rs2455873	snp	G/T	0	0	intron-variant	TFG	GRCh38.p7	3:100729493	AACACATACTTAAAG[G/T]TCAGTCCACATTTTA	10342
rs2455874	snp	G/T	0.00199481	0.0315187	intron-variant	TFG	GRCh38.p7	3:100718618	GCTGGAGTACAGTGG[G/T]GTGATCTTGGCTCAC	10342
rs2460720	snp	A/T	0	0	intron-variant	TFG	GRCh38.p7	3:100732131	TGGGCACTCTGGAAA[A/T]AATAATTATAGGAAC	10342
rs2929616	snp	G/T			intron-variant	TFG	GRCh38.p7	3:100722401	AAATATTCTGGATGT[G/T]CTCATTTTCAACTTC	10342
rs2947093	snp	G/T	0.5	0	intron-variant	TFG	GRCh38.p7	3:100718550	CTTTGTATTTCATGG[G/T]TTTTTTTTTTTTTTT	10342
rs3057194	in-del	-/TTTA	0.375	0.216506	intron-variant	TFG	GRCh38.p7	3:100728367	TAAATTTAATAAATA[-/TTTA]AGAACAGCATGAAAT	10342
rs3087787	snp	A/T	0.443598	0.158176	intron-variant	TFG	GRCh38.p7	3:100742598	GTTAGGTTACTTAGC[A/T]TGTCTAAATGATCTC	10342
rs3101519	snp	A/C			intron-variant	TFG	GRCh38.p7	3:100718471	ttttgtccgttggtc[A/C]cagttcatggaccct	10342
rs3102101	snp	A/T			intron-variant	TFG	GRCh38.p7	3:100718479	TCAAGCTAAGGGTCC[A/T]TGAACTGGGACCAAC	10342
rs3773921	snp	A/G	0.427575	0.175975	intron-variant	TFG	GRCh38.p7	3:100736295	CATGTCTGCAATGCC[A/G]ATATCCCCCTACTCC	10342
rs3773922	snp	A/G	0.459574	0.136304	intron-variant	TFG	GRCh38.p7	3:100730657	CACATTTCTTGGTGA[A/G]GGTAAGCCACAGGTT	10342
rs3773924	snp	C/T	0.42803	0.175514	intron-variant	TFG	GRCh38.p7	3:100729865	TATCATTAACATAAT[C/T]CCATATGACTATTAG	10342
rs3796275	snp	C/G	0.00199481	0.0315187	intron-variant	TFG	GRCh38.p7	3:100747134	TGACTATTTCCATAT[C/G]TCTCAATCAAATTCA	10342
rs3796276	snp	C/T	0.443464	0.15834	intron-variant	TFG	GRCh38.p7	3:100746765	CACCTGAAATCTGAA[C/T]TGTTTTTTTTTAACT	10342
rs3821726	snp	C/T	0.137867	0.223442	intron-variant	TFG	GRCh38.p7	3:100711924	ACACAACCAACTCTT[C/T]GCCTTCTGCAATGCC	10342
rs3830581	in-del	-/C	0.419944	0.183355	intron-variant	TFG	GRCh38.p7	3:100736766	CAATGCTGTAATAAA[-/C]ACTTCTACACATGTA	10342
rs3832236	in-del	-/A	0.448323	0.15221	intron-variant	TFG	GRCh38.p7	3:100747343	GCATTAAAAAAAAAA[-/A]GGATTGAATGAATTT	10342
rs3839089	in-del	-/T			intron-variant	TFG	GRCh38.p7	3:100747032	GACCCTGACTAAATT[-/T]ATTAAGAGCAAGCTT	10342
rs3841652	in-del	-/T	0.0626037	0.165477	intron-variant	TFG	GRCh38.p7	3:100732184	TTTTTTGGTTTTTTT[-/T]GGAGCCCAATAACCT	10342
rs4928085	snp	C/T	0.428182	0.17536	intron-variant	TFG	GRCh38.p7	3:100733729	AGTGACTTGGACTTA[C/T]ATTCTTTTGAGGATT	10342
rs4928086	snp	G/T	0.42803	0.175514	intron-variant	TFG	GRCh38.p7	3:100741759	taccattttttatct[G/T]ttttgccatattttc	10342
rs5851219	in-del	-/C			intron-variant	TFG	GRCh38.p7	3:100735569	ACAGCTAGTGAGTGA[-/C]AGCACTAGGATTTGA	10342
rs5851220	in-del	-/AAAC	0.5	0	downstream-variant-500B	TFG, ABI3BP	GRCh38.p7	3:100749209	GTTAATTTAGGACAT[-/AAAC]AAACAAACAGTAGAT	10342
rs6772054	snp	A/C	0.00265044	0.036307	missense	TFG	GRCh38.p7	3:100748418	CCAAGACCAGGTTTT[A/C]CTTCACTTCCTGGAA	10342
rs6773482	snp	C/G	0.409041	0.192888	intron-variant, upstream-variant-2KB, utr-variant-5-prime	TFG	GRCh38.p7	3:100710003	CCAGGAGGCGCGCCT[C/G]GGGGGCTCCGGGAGG	10342
rs6775161	snp	A/G	0.481087	0.0953875	intron-variant	TFG	GRCh38.p7	3:100719048	AATGTGTTTATGAAA[A/G]TTGAACATTAAACAA	10342
rs6777552	snp	A/G	0.0456336	0.143994	intron-variant	TFG	GRCh38.p7	3:100711664	TTCTAGGTGCTGCTG[A/G]GAATAGATAGTACCA	10342
rs6777763	snp	A/G	0.459687	0.136129	intron-variant	TFG	GRCh38.p7	3:100711831	ATATTTACCATCTTG[A/G]TGAAGTAATTATACT	10342
rs6806786	snp	C/T	0.459118	0.137002	upstream-variant-2KB	TFG	GRCh38.p7	3:100708142	gcttaacagacaaga[C/T]tgaaaacctaactta	10342
rs6810101	snp	C/T	0.43221	0.171171	upstream-variant-2KB	TFG	GRCh38.p7	3:100709093	ATAGGCTCCCAATAA[C/T]GAATGAATGGATTTA	10342
rs7431500	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100734533	GGTCAGCGCTTTTAA[C/T]TCTTATCCATTCTAA	10342
rs7617184	snp	A/G	0.465683	0.126415	intron-variant	TFG	GRCh38.p7	3:100739416	ACCAAAAGGGATAAT[A/G]TTACTCTTTTTCATA	10342
rs7620552	snp	A/G	0.0256215	0.110247	intron-variant, upstream-variant-2KB	TFG	GRCh38.p7	3:100710649	TGGTTCAGGAGGCAG[A/G]CTTTTTATATGACCT	10342
rs7620718	snp	A/T	0.0111196	0.0737302	intron-variant	TFG	GRCh38.p7	3:100724157	atattagtaaaCTGG[A/T]TTGGAAATTTTTGAG	10342
rs7629427	snp	C/T	0.0248432	0.108648	intron-variant	TFG	GRCh38.p7	3:100726286	cagcaagcaaactta[C/T]cctaccttcttctgc	10342
rs7635652	snp	A/G	0.409721	0.192325	intron-variant	TFG	GRCh38.p7	3:100720979	AACTTAGAGTTCAGT[A/G]TGAAATATGATCATG	10342
rs7637250	snp	C/G	0.409041	0.192888	intron-variant	TFG	GRCh38.p7	3:100726311	ttctgcctgttttgt[C/G]atagctgcactggca	10342
rs7637272	snp	C/G	0.409041	0.192888	intron-variant	TFG	GRCh38.p7	3:100726398	gactcaaatgtcagt[C/G]tcctctggcaacacc	10342
rs7645118	snp	C/T	0.0260105	0.111035	intron-variant	TFG	GRCh38.p7	3:100731279	GTTTGTTTCTTTTGA[C/T]GTCTTTTGTATCTTG	10342
rs7645141	snp	C/T	0.00119737	0.0244387	intron-variant	TFG	GRCh38.p7	3:100746221	TAGTCATCATTTAAT[C/T]TCGGGATTTCGGTCC	10342
rs7647299	snp	C/T	0.0252325	0.109451	intron-variant	TFG	GRCh38.p7	3:100737203	GCAATATGTCTTTAA[C/T]GGAAAAAAAGCAGTG	10342
rs7650690	snp	A/G	0.459687	0.136129	intron-variant	TFG	GRCh38.p7	3:100714585	TTTTTTACAAGCATT[A/G]TTTTCTCCTTTTGTC	10342
rs7653531	snp	C/T	0.481087	0.0953875	intron-variant	TFG	GRCh38.p7	3:100714953	TGCCTTCTTTGTTAA[C/T]ATCTCTGCTGAAATT	10342
rs7653838	snp	A/C	0	0	intron-variant	TFG	GRCh38.p7	3:100745560	TATTTAAGTATGATA[A/C]ATATTATTAATGTAA	10342
rs9809520	snp	A/G/T	0.0626037	0.165477	intron-variant	TFG	GRCh38.p7	3:100737562	GGGACCTTTAAAGCC[A/G/T]CATTCCACTTCAAAA	10342
rs9811878	snp	A/G	0.466515	0.124985	intron-variant	TFG	GRCh38.p7	3:100716383	acttcattctttttt[A/G]tggctgaattgtatt	10342
rs9811997	snp	A/T	0.0622301	0.165053	intron-variant	TFG	GRCh38.p7	3:100746510	GATGTCCTATGTATT[A/T]AAAAAAAAACTCACA	10342
rs9817550	snp	A/C	0.0368353	0.130617	intron-variant	TFG	GRCh38.p7	3:100747727	GATTAGTACAATAAG[A/C]TGTATTTATAGTATT	10342
rs9817756	snp	A/G	0.0352966	0.128072	intron-variant	TFG	GRCh38.p7	3:100747864	GTCTTCCTAGAAAGT[A/G]TAATTCTTTCATTTA	10342
rs9818055	snp	A/G	0.0622301	0.165053	intron-variant	TFG	GRCh38.p7	3:100742076	CTCTTCATATATCCT[A/G]TAGATCTCTCAAGTA	10342
rs9824942	snp	A/T	0.499743	0.0113364	intron-variant	TFG	GRCh38.p7	3:100713908	TTTTAAAGTCTTTTT[A/T]AAAAAAAAAAAAAAA	10342
rs9825075	snp	A/G	0.0543475	0.155628	intron-variant	TFG	GRCh38.p7	3:100713923	AAAAAAAAAAAAAAA[A/G]agacagagcctctgt	10342
rs9830473	snp	C/G	0.0134861	0.0810011	intron-variant	TFG	GRCh38.p7	3:100723845	AGTTTTTTTTTTTTT[C/G]GAGTACTCATAGTGC	10342
rs9833043	snp	A/G	0.0622301	0.165053	intron-variant	TFG	GRCh38.p7	3:100720347	TTTTAATTTAGCTGT[A/G]TTAGAATTTTTAAAT	10342
rs9834987	snp	A/T	0.0622301	0.165053	intron-variant	TFG	GRCh38.p7	3:100745694	AGAAATAATTTATGC[A/T]GGTTGAATCTAGTCT	10342
rs9839133	snp	A/G	0.0622301	0.165053	intron-variant	TFG	GRCh38.p7	3:100721826	tagtctacaaaatta[A/G]aagttatttaagaca	10342
rs9840505	snp	A/G	0.431769	0.17164	intron-variant	TFG	GRCh38.p7	3:100718966	CTGTTTCTGTTGTAG[A/G]ATTCAGAAAAGAAAA	10342
rs9843956	snp	A/G	0.443866	0.157848	intron-variant	TFG	GRCh38.p7	3:100722419	atccagaatatttct[A/G]ttcagagtttcaaga	10342
rs9850735	snp	A/G	0.0368353	0.130617	intron-variant	TFG	GRCh38.p7	3:100720612	gaactgacaggaggc[A/G]gagcccaccacttaa	10342
rs9853377	snp	C/T	0.0577344	0.159793	upstream-variant-2KB	TFG	GRCh38.p7	3:100708409	tcgtgaaatcgttca[C/T]tgctcaattaaactc	10342
rs9853496	snp	C/G	0.0622301	0.165053	intron-variant	TFG	GRCh38.p7	3:100726010	tacaaggcgaagtcc[C/G]gtgataggccatctg	10342
rs9853591	snp	C/T	0.0622301	0.165053	intron-variant	TFG	GRCh38.p7	3:100723666	aattcactaggacta[C/T]atagcaatctgaaca	10342
rs9853596	snp	C/T	0.0622301	0.165053	intron-variant	TFG	GRCh38.p7	3:100723686	caatctgaacactta[C/T]gcatgttagctttag	10342
rs9855255	snp	A/G	0.0368353	0.130617	intron-variant	TFG	GRCh38.p7	3:100724888	atgttgaaaagtcgt[A/G]gcaaactatgaataa	10342
rs9859204	snp	C/T	0.040671	0.13668	intron-variant	TFG	GRCh38.p7	3:100739807	ttcagtatatatgtc[C/T]aactgataatcttct	10342
rs9859445	snp	A/G	0.0622301	0.165053	intron-variant	TFG	GRCh38.p7	3:100725186	gcagggattacagat[A/G]tgagccaccacgcct	10342
rs9859730	snp	A/T	0.0622301	0.165053	intron-variant	TFG	GRCh38.p7	3:100725326	TATATACAACAAAAG[A/T]TACTTGGGATAAATC	10342
rs9861416	snp	A/G	0.0622301	0.165053	intron-variant	TFG	GRCh38.p7	3:100722635	TTAAAAGTAGCCAGA[A/G]AGAATAAGACTGATC	10342
rs9863695	snp	C/T	0.0360663	0.129354	intron-variant	TFG	GRCh38.p7	3:100740252	tttagacagatatcc[C/T]ggaatggtttagctg	10342
rs9866866	snp	A/G	0.0622301	0.165053	intron-variant	TFG	GRCh38.p7	3:100723769	aattatggGAGAGCC[A/G]ATAAATCAAGCAGGC	10342
rs9868472	snp	C/T	0.0573587	0.15934	intron-variant	TFG	GRCh38.p7	3:100746984	TACCATGAGTTAATG[C/T]GTTAAAGATACTTGA	10342
rs9870028	snp	C/T	0.0622301	0.165053	intron-variant	TFG	GRCh38.p7	3:100741922	gtagtaggctatata[C/T]atctaggtttgtgta	10342
rs9871767	snp	A/C/G	0.0622301	0.165053	intron-variant	TFG	GRCh38.p7	3:100724482	GAAGTAGAAAAATTG[A/C/G]TTGCCCCAATTAACA	10342
rs9876383	snp	G/T	0.432797	0.170544	intron-variant	TFG	GRCh38.p7	3:100725098	TTTTTAGTAGAGACG[G/T]GGTTTCACCGTGTTA	10342
rs9881780	snp	A/T	0.0622301	0.165053	intron-variant	TFG	GRCh38.p7	3:100739259	TGTGTTAATAGTCCA[A/T]ACTAAAATTAAGAAT	10342
rs9881943	snp	G/T	0.0622301	0.165053	intron-variant	TFG	GRCh38.p7	3:100739355	TAGTCTTAATATGTT[G/T]TTCAGTTAAAAGGAT	10342
rs9883133	snp	A/C			downstream-variant-500B	TFG, ABI3BP	GRCh38.p7	3:100749104	TCCATTCAGAGAAAA[A/C]AGTGCCATTTGGTTT	10342
rs9883418	snp	C/T	0.0622301	0.165053	intron-variant	TFG	GRCh38.p7	3:100719137	GTTTTGTCATCTTTG[C/T]CCAAAATAAATCCAA	10342
rs10537172	in-del	-/A	0.5	0	intron-variant	TFG	GRCh38.p7	3:100738098	AAAACAAACAAAGCC[-/A]AAAAAAAAAAAATCC	10342
rs10936343	snp	C/T	0.421209	0.182174	intron-variant	TFG	GRCh38.p7	3:100732936	AAAGAATAAGCACTG[C/T]TGGGTTCAAGTAAAT	10342
rs10936345	snp	C/G	0.45946	0.136478	intron-variant	TFG	GRCh38.p7	3:100733800	ACttaacataaataa[C/G]aaacagaaaagcgct	10342
rs10936346	snp	C/G	0.45946	0.136478	intron-variant	TFG	GRCh38.p7	3:100733824	aagcgctctctaaaa[C/G]aaaaaggtatttggg	10342
rs10936349	snp	C/T	0.409041	0.192888	intron-variant	TFG	GRCh38.p7	3:100735015	CAAACATGGAATGAA[C/T]ATTAACTGTAATAAA	10342
rs11342443	in-del	-/T	0.463451	0.130149	intron-variant	TFG	GRCh38.p7	3:100714568	ACATTTTCACATACA[-/T]TTTTTTTACAAGCAT	10342
rs11354328	in-del	-/T	0.452965	0.145963	intron-variant	TFG	GRCh38.p7	3:100711104	GTATACGTGACTCAA[-/T]TTTTTTTTTTTTTTG	10342
rs11557849	snp	C/G			intron-variant, utr-variant-5-prime, upstream-variant-2KB	TFG	GRCh38.p7	3:100709672	GGCCTCGCGTCCGCC[C/G]ATTCAGCGGAGACCT	10342
rs11557850	snp	A/T	0.00491398	0.0493238	stop-gained	TFG	GRCh38.p7	3:100713725	GGGAAGCTAATCATC[A/T]AAGCTCAACTTGGGG	10342
rs11716198	snp	A/C			intron-variant	TFG	GRCh38.p7	3:100725284	ATATAAAAGGATTAT[A/C]AATGTAACTAAAATA	10342
rs12493765	snp	A/C	0.0372196	0.131242	upstream-variant-2KB	TFG	GRCh38.p7	3:100709228	AAGTTTAGAACAGCG[A/C]ACTACGCCCCGCCCA	10342
rs12494895	snp	C/T	0.0154538	0.0865337	intron-variant, utr-variant-5-prime	TFG	GRCh38.p7	3:100711008	GCTTTAGGAAAGAAG[C/T]ACTGGTTCCTGGCCA	10342
rs12495397	snp	A/G	0.431325	0.172108	upstream-variant-2KB	TFG	GRCh38.p7	3:100707682	TTGTGGTTTTACCCC[A/G]TCCCAAACCATCTTA	10342
rs12631524	snp	G/T			intron-variant	TFG	GRCh38.p7	3:100718660	catcccaggttcaag[G/T]gattctcctgcctcg	10342
rs13059686	snp	C/T	0.459574	0.136304	intron-variant	TFG	GRCh38.p7	3:100714131	CCCATCCTCTCTTCA[C/T]GGTAGTTGAGACCTC	10342
rs13073146	snp	G/T	0.428333	0.175206	intron-variant	TFG	GRCh38.p7	3:100717687	tgcattttttatttt[G/T]tattgtatgtgtata	10342
rs13078643	snp	C/T	0.427575	0.175975	intron-variant	TFG	GRCh38.p7	3:100740531	TGGTATACAGGTCAG[C/T]CCTATTCAGTATGTG	10342
rs13086822	snp	A/G	0.427575	0.175975	intron-variant	TFG	GRCh38.p7	3:100724264	AAATTGGAATTGTTA[A/G]GATCAACAATTTTGA	10342
rs13087035	snp	C/T	0	0	intron-variant	TFG	GRCh38.p7	3:100744804	TAAACATGCCTTTTT[C/T]CCTTGTGTGTGTGTG	10342
rs13090850	snp	A/C			intron-variant	TFG	GRCh38.p7	3:100726581	ACTGAGTAGATAATA[A/C]CAGATTATAGGCCAT	10342
rs13092027	snp	C/T	0.45946	0.136478	intron-variant	TFG	GRCh38.p7	3:100745140	GTGGGGAGATAAAAC[C/T]TACAGTAGATGATTC	10342
rs13100523	snp	A/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	TFG	GRCh38.p7	3:100710384	TTTCGAATGTGATGA[A/G]AGTGAGCCTTGGAGG	10342
rs13315123	snp	C/T	0.0622301	0.165053	intron-variant	TFG	GRCh38.p7	3:100716089	tcaatattctccttc[C/T]agctatttgaaatta	10342
rs13316513	snp	C/T	0.0622301	0.165053	intron-variant	TFG	GRCh38.p7	3:100742693	agaatgtgcagactc[C/T]acacagaacagtaac	10342
rs13317522	snp	C/G	0.0622301	0.165053	intron-variant	TFG	GRCh38.p7	3:100728474	TACCAAACCTTTTTA[C/G]CAGTAAGGTCATAGG	10342
rs13317752	snp	A/G	0.0629771	0.165899	intron-variant	TFG	GRCh38.p7	3:100744514	CTCACTTGGCTTTTA[A/G]TGAACATTAGCGTTA	10342
rs13318765	snp	A/G	0.0573587	0.15934	intron-variant	TFG	GRCh38.p7	3:100717781	gttctaagggttttg[A/G]tagagtttttaggtt	10342
rs13318793	snp	C/G	0.0622301	0.165053	intron-variant	TFG	GRCh38.p7	3:100717904	ctctggctagtactt[C/G]cTTAACTGTCttttt	10342
rs13319530	snp	C/T	0.0622301	0.165053	intron-variant	TFG	GRCh38.p7	3:100715796	catgattatagctca[C/T]cataacctttaactc	10342
rs13325014	snp	C/G	0.0626037	0.165477	intron-variant	TFG	GRCh38.p7	3:100716927	atgtttgagttcctt[C/G]tatattctgaatatt	10342
rs13326828	snp	C/T	0.0622301	0.165053	intron-variant	TFG	GRCh38.p7	3:100718288	AACTGACCTCATTGA[C/T]TGGCTTTCTCTTAAC	10342
rs13327329	snp	A/G	0.0622301	0.165053	intron-variant	TFG	GRCh38.p7	3:100731667	gttcaagtgattctc[A/G]tgactcagcctcctg	10342
rs13433681	snp	A/G	0.0577344	0.159793	upstream-variant-2KB	TFG	GRCh38.p7	3:100707371	CAAGTTGCTTTCGGA[A/G]TCCATGAGCTCCATG	10342
rs13433684	snp	A/G	0.0577344	0.159793	upstream-variant-2KB	TFG	GRCh38.p7	3:100707436	GCCTCTCTTCCTAGC[A/G]TACAGATGACCACAG	10342
rs13434023	snp	C/T	0.0577344	0.159793	upstream-variant-2KB	TFG	GRCh38.p7	3:100707367	GCCTCAAGTTGCTTT[C/T]GGAGTCCATGAGCTC	10342
rs16842638	snp	G/T	0.0622301	0.165053	intron-variant	TFG	GRCh38.p7	3:100715003	AGTGTTTTTTACTGT[G/T]GAACTTACTTGCAGT	10342
rs16842640	snp	A/G	0.0134861	0.0810011	intron-variant	TFG	GRCh38.p7	3:100719410	GATCTGGGGGATTTC[A/G]CGGTCATAAATACAC	10342
rs16842674	snp	C/T	0.030665	0.119967	intron-variant	TFG	GRCh38.p7	3:100738124	TGTCTGTTGGATGAA[C/T]ACCAGTCATTATGGA	10342
rs16842679	snp	C/T	0.0622301	0.165053	intron-variant	TFG	GRCh38.p7	3:100743731	TAATAGAGTGGGCTC[C/T]GTCTCATTTTCTAAG	10342
rs28364602	snp	A/G	0.137867	0.223442	upstream-variant-2KB	TFG	GRCh38.p7	3:100709222	CTCAAAAAGTTTAGA[A/G]CAGCGCACTACGCCC	10342
rs28380383	snp	A/G	0.0622301	0.165053	intron-variant	TFG	GRCh38.p7	3:100729853	TCTTCCTGTCTTCTA[A/G]TAGTCATATGGAATT	10342
rs28469597	snp	A/G	0.0626037	0.165477	intron-variant	TFG	GRCh38.p7	3:100723881	AGAAGTTGACTGTAA[A/G]TCAAGTCTTCCAGAA	10342
rs28523825	snp	A/G	0.0622301	0.165053	intron-variant	TFG	GRCh38.p7	3:100737988	TGTTTGCATTGTTGA[A/G]TTGAAGTGGGTGGTC	10342
rs28530760	snp	A/G	0.0622301	0.165053	intron-variant	TFG	GRCh38.p7	3:100737916	TTAAAAAAATTAGCC[A/G]GGTGCTATGGCATGT	10342
rs34095495	in-del	-/A			intron-variant	TFG	GRCh38.p7	3:100741359	ATAGGCCTAGGCTAA[-/A]TGTGTATGTTTGTGT	10342
rs34112649	snp	C/G			missense	TFG	GRCh38.p7	3:100736617	CGTTCAGGAACACCC[C/G]ACAGCATTGCTTCCT	10342
rs34219697	in-del	-/A			intron-variant	TFG	GRCh38.p7	3:100739572	AGCATATAATTAAAA[-/A]TCTTTAAAATCATAT	10342
rs34256650	in-del	-/T			intron-variant	TFG	GRCh38.p7	3:100718242	TTTAACTGCCTTTTT[-/T]CCCACTTGAAGATGC	10342
rs34440147	snp	C/G			intron-variant	TFG	GRCh38.p7	3:100747971	AAATTGTAGAGAATG[C/G]CTCTTTGATAACTAC	10342
rs34584213	in-del	-/A			intron-variant	TFG	GRCh38.p7	3:100747814	AGGTCTCCCCTGAAA[-/A]CCTGGTTAATGACTA	10342
rs34654372	in-del	-/G			intron-variant	TFG	GRCh38.p7	3:100721529	CGTCAGGGGCTTGGG[-/G]AAGTCTCCCTTCAGG	10342
rs34733412	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100741934	ATACATCTAGGTTTG[C/T]GTAAGTATACTATAT	10342
rs34793873	in-del	-/C			splice-acceptor-variant	TFG	GRCh38.p7	3:100719972	TTTTTTTTAAATTCC[-/C]AGATGGAGATCTTAT	10342
rs34803009	in-del	-/C			intron-variant	TFG	GRCh38.p7	3:100726412	TGTCCTCTGGCAACA[-/C]CCCTCACAGACACAC	10342
rs34848913	snp	C/T	0.0115144	0.0749975	intron-variant	TFG	GRCh38.p7	3:100737740	ATAGAATCCTATCAT[C/T]CTGTGGTGATACTTT	10342
rs34857143	in-del	-/AAAC/AACA	0	0	downstream-variant-500B	TFG, ABI3BP	GRCh38.p7	3:100749210	GGACATAAACAAACA[-/AAAC/AACA]GTAGATATAATGGGG	10342
rs34860451	in-del	-/G	0.427271	0.176281	intron-variant	TFG	GRCh38.p7	3:100720281	CAGAGTGTTAAGTAT[-/G]TTTTTTTTGAAATCA	10342
rs34892615	in-del	-/A			intron-variant	TFG	GRCh38.p7	3:100723985	AATATGTAACCCAAA[-/A]TTTCCCTACTTTTGG	10342
rs35122746	in-del	-/C			intron-variant	TFG	GRCh38.p7	3:100723336	AGAAAAAAAGAAAAC[-/C]AAGGGTACCTGTTCA	10342
rs35133199	in-del	-/A			intron-variant	TFG	GRCh38.p7	3:100739551	GACAGCCTAAAAAAA[-/A]TGAAAAAGCATATAA	10342
rs35152775	in-del	-/A	0.455263	0.142713	intron-variant	TFG	GRCh38.p7	3:100742890	ATGCAAAAAAAAAAA[-/A]GCTTTATGAAGAGTT	10342
rs35235686	in-del	-/T			intron-variant	TFG	GRCh38.p7	3:100727852	TTTTTTAAAATTTTT[-/T]GAGACAAGGTCTCCC	10342
rs35239192	in-del	-/T			intron-variant	TFG	GRCh38.p7	3:100734506	GTGGTTTTCTGCCAT[-/T]GGAGCTGCAGAGGTC	10342
rs35353873	snp	C/T	0.430583	0.172886	upstream-variant-2KB	TFG	GRCh38.p7	3:100707633	AGTAGTATAATTCAC[C/T]TCCTTCAGGGAATAT	10342
rs35367963	in-del	-/C			intron-variant	TFG	GRCh38.p7	3:100747841	ACTATTTAGCTTTCC[-/C]ATTTTTGGTCTTCCT	10342
rs35393997	in-del	-/G			intron-variant	TFG	GRCh38.p7	3:100734930	TTGTAGTTCTTCAGG[-/G]TGTGATGTGGTAAAA	10342
rs35420245	in-del	-/A			intron-variant	TFG	GRCh38.p7	3:100725823	ACATATTAAGCTTTA[-/A]CAAAGATGGGTGTTT	10342
rs35446602	snp	C/T	0.0425829	0.139564	intron-variant	TFG	GRCh38.p7	3:100740385	CCATTTGGACTTCTC[C/T]ATGGGGCTGCTTGGG	10342
rs35495062	in-del	-/TT	0.45946	0.136478	intron-variant	TFG	GRCh38.p7	3:100745180	TTGTAGTATAAAAAG[-/TT]TTTAATACAAAGCTG	10342
rs35496426	in-del	-/G			intron-variant, upstream-variant-2KB	TFG	GRCh38.p7	3:100710896	TGAAGTAATGTTGGG[-/G]TTGGGATTTCCCCTT	10342
rs35648279	snp	C/T	0.0255488	0.110098	synonymous-codon	TFG	GRCh38.p7	3:100732644	ATCTGTTAAGCCAAA[C/T]GCTGACATAACATTT	10342
rs35685595	in-del	-/C/G/GT	0.0107246	0.0724382	intron-variant	TFG	GRCh38.p7	3:100744806	ACATGCCTTTTTTCC[-/C/G/GT]TTGTGTGTGTGTGTG	10342
rs35896919	multinucleotide-polymorphism	GG/TC			intron-variant	TFG	GRCh38.p7	3:100748014	TATTATGTGATGGAA[GG/TC]TACCACTCTGCTTGT	10342
rs35955581	in-del	-/T			intron-variant	TFG	GRCh38.p7	3:100743027	AATCTCAGCCTTTTT[-/T]GATGATGCCCAAGTT	10342
rs36116984	in-del	-/C	0.409041	0.192888	intron-variant	TFG	GRCh38.p7	3:100725676	GTGCGTGCCTGTAAT[-/C]CCAGCCACTTGGGAG	10342
rs41272979	snp	A/G/T	0.0253053	0.109601	intron-variant	TFG	GRCh38.p7	3:100744825	TGTGTGTGTGTGTGT[A/G/T]TTTTCAGGTCAGATG	10342
rs41373752	snp	A/G	0.430583	0.172886	intron-variant	TFG	GRCh38.p7	3:100740152	ATGTTTCTAAAATCA[A/G]AACTATGTGTATTAT	10342
rs55662971	snp	A/G	0.00279162	0.0372561	intron-variant	TFG	GRCh38.p7	3:100747612	AAGTAAAAATTTTGA[A/G]TTGTAAAGGCAAAAA	10342
rs55750598	in-del	-/T	0	0	intron-variant	TFG	GRCh38.p7	3:100717594	GTTTTTTTTTTTTTT[-/T]GTAGAGGTTTTTCAT	10342
rs57230594	in-del	-/GTAGT			intron-variant	TFG	GRCh38.p7	3:100745014	TTAATTCCTTGATTT[-/GTAGT]ACATTGATATAATAG	10342
rs57611480	in-del	-/TTTT	0	0	intron-variant	TFG	GRCh38.p7	3:100718572	TTTTTTTTTTTTTTT[-/TTTT]GAGACAAAGTCTTGC	10342
rs57687306	snp	C/T	0.0622301	0.165053	intron-variant	TFG	GRCh38.p7	3:100718600	TCTTGCTTTGTCGTT[C/T]AGGCTGGAGTACAGT	10342
rs59027223	snp	G/T	0.5	0	intron-variant	TFG	GRCh38.p7	3:100718553	TGTATTTCATGGTTT[G/T]TTTTTTTTTTTTTTT	10342
rs59789493	snp	C/T	0.00676609	0.0577691	intron-variant	TFG	GRCh38.p7	3:100735541	AGAGATTATGTAACA[C/T]GTCCAGAGTTACACA	10342
rs61204459	in-del	-/AA	0.434223	0.169003	intron-variant	TFG	GRCh38.p7	3:100738086	AAAACAAACAAAGCC[-/AA]AAAAAAAAAAATCCA	10342
rs61230753	snp	G/T	0.131702	0.22024	intron-variant	TFG	GRCh38.p7	3:100744807	ACATGCCTTTTTTCC[G/T]TGTGTGTGTGTGTGT	10342
rs61736338	snp	A/G	0.00898133	0.0664078	synonymous-codon	TFG	GRCh38.p7	3:100748273	ACTGCCTGCTCAGCC[A/G]CCACAGCAGTACCAG	10342
rs62274023	snp	C/T	0.00438332	0.0466095	upstream-variant-2KB	TFG	GRCh38.p7	3:100708363	TCTGCTGGAGTCTCT[C/T]AATCTGCTGTGATTC	10342
rs62274024	snp	A/C			intron-variant	TFG	GRCh38.p7	3:100715837	GCAATACTGCCAACC[A/C]GGCCTCCCAAAGGCA	10342
rs62274025	snp	C/T	0.0267878	0.112589	intron-variant	TFG	GRCh38.p7	3:100716672	TAATGTGTAAGAGTT[C/T]CCTTTTCTCTTCATT	10342
rs62274049	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100747341	TCAAATTCATTCAAT[C/T]CTTTTTTTTTTTAAT	10342
rs63670060	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100747343	GCATTAAAAAAAAAA[A/G]GGATTGAATGAATTT	10342
rs66530346	in-del	-/AGTG			downstream-variant-500B	TFG, ABI3BP	GRCh38.p7	3:100749258	CCTGAATAAAACTTA[-/AGTG]GTGATTTTCCTTCTC	10342
rs66907338	in-del	-/TATT	0.432651	0.170701	intron-variant	TFG	GRCh38.p7	3:100728365	ATTAAATTTAATAAA[-/TATT]TAAGAACAGCATGAA	10342
rs66999419	in-del	-/A	0.0626037	0.165477	intron-variant	TFG	GRCh38.p7	3:100746754	CCCAGTTAAAAAAAA[-/A]CAATTCAGATTTCAG	10342
rs67862637	in-del	-/A			downstream-variant-500B	TFG, ABI3BP	GRCh38.p7	3:100749274	TGATTTTCCTTCTCG[-/A]ATAAAAGGTATAGTT	10342
rs71132531	in-del	-/TCAAATCAACTATACCTTTTATCTGAGAAGGAAAATCAC	0	0	downstream-variant-500B	TFG, ABI3BP	GRCh38.p7	3:100749262	TATCTAGAAGGAAAA[lengthTooLong]TCACTAAGTTTTATT	10342
rs71625567	in-del	-/TTA	0.479984	0.0980171	intron-variant	TFG	GRCh38.p7	3:100729583	ATTTAAAGAAAACTC[-/TTA]TTATTATTTTTTTCT	10342
rs72919404	snp	C/G	0.0126979	0.078662	upstream-variant-2KB	TFG	GRCh38.p7	3:100707832	TCTTCTGCAGTACTC[C/G]ACTCCCTTATCCCTG	10342
rs72919406	snp	C/T	0.0126979	0.078662	upstream-variant-2KB	TFG	GRCh38.p7	3:100707978	AGATCACACTACTTA[C/T]GGTTGTAAAAGAACG	10342
rs72919417	snp	G/T	0.0463947	0.145069	intron-variant, upstream-variant-2KB, utr-variant-5-prime	TFG	GRCh38.p7	3:100709442	CCTGGGTATGTCCAC[G/T]CGCAATAAGGAGGGG	10342
rs72919423	snp	A/C	0.0622301	0.165053	intron-variant	TFG	GRCh38.p7	3:100711893	GTAGTTCCTGAATAC[A/C]GAAAGCATTGCAGAA	10342
rs72919426	snp	C/T	0.0622301	0.165053	intron-variant	TFG	GRCh38.p7	3:100711967	TAATCACTGTCTTCA[C/T]GAGAAGTCCATTGTG	10342
rs72919429	snp	G/T	0.0352966	0.128072	intron-variant	TFG	GRCh38.p7	3:100712171	TGAGGGGTCTAGAGA[G/T]ATTAATTTAAGGACT	10342
rs72919433	snp	A/G	0.0622301	0.165053	intron-variant	TFG	GRCh38.p7	3:100715307	GCATTGACATTGGCA[A/G]GCAGATGAGTGAAGA	10342
rs72919437	snp	G/T	0.0123036	0.0774623	intron-variant	TFG	GRCh38.p7	3:100715687	ACATTGATTTGCACC[G/T]CTGTGACTTTGAAAT	10342
rs72928625	snp	A/G/T	0.0122112	0.0771805	intron-variant	TFG	GRCh38.p7	3:100732722	TTCCTTCATCTTTCC[A/G/T]TTCTTCCCTTTCCTT	10342
rs72928626	snp	A/G	0.0622301	0.165053	intron-variant	TFG	GRCh38.p7	3:100732998	AATCTGAACTATTTT[A/G]TAATTTGATTAGTTG	10342
rs72928628	snp	C/G	0.0573587	0.15934	intron-variant	TFG	GRCh38.p7	3:100734032	GGCAGTTTCTGGGCA[C/G]ATGTCCTCACAGTCA	10342
rs72928630	snp	A/G	0.0577344	0.159793	intron-variant	TFG	GRCh38.p7	3:100734129	TTGAACTCTTTTGTG[A/G]TAGTTTTTGCAAGAA	10342
rs72928632	snp	C/G/T	0.0622301	0.165053	intron-variant	TFG	GRCh38.p7	3:100734341	TCTTGAGATATCCTC[C/G/T]TCTGCTCTCCCAGCC	10342
rs72928634	snp	G/T	0.0622301	0.165053	intron-variant	TFG	GRCh38.p7	3:100734401	GTATATACCTAGATC[G/T]TGGGTCTTACCCTTT	10342
rs72928638	snp	C/T	0.0221141	0.102801	intron-variant	TFG	GRCh38.p7	3:100735712	TTGACTGTCACAGCA[C/T]TGGAACTGTAATATA	10342
rs72928641	snp	C/T	0.0368353	0.130617	intron-variant	TFG	GRCh38.p7	3:100736958	ATACAGAGTGAAAGA[C/T]CAGTCATTAGTCAGT	10342
rs72928650	snp	A/G	0.0182019	0.0936463	intron-variant	TFG	GRCh38.p7	3:100740995	CACAAGGCATTACTT[A/G]CGTGTTTGTGGTGAT	10342
rs72928653	snp	C/T	0.0126979	0.078662	intron-variant	TFG	GRCh38.p7	3:100742262	AATTGTAACTTTAAG[C/T]GAGATGACGTATGAG	10342
rs72928658	snp	C/T	0.0573587	0.15934	intron-variant	TFG	GRCh38.p7	3:100743418	GTTAGTTATGAAGTA[C/T]AATCCAGGATTAAGG	10342
rs72928662	snp	C/G	0.0622301	0.165053	intron-variant	TFG	GRCh38.p7	3:100743657	TAAACATAGTTGTAT[C/G]TCCTTTAGTGCTACC	10342
rs72928666	snp	A/G	0.0126979	0.078662	intron-variant	TFG	GRCh38.p7	3:100743694	TAAAAACTTAGACAC[A/G]TATAGGGCTGAGCAG	10342
rs72928670	snp	A/G	0.0126979	0.078662	intron-variant	TFG	GRCh38.p7	3:100744029	TAAAGACATAAACCA[A/G]TAAATCTTTGCTTGA	10342
rs72928677	snp	G/T	0.0622301	0.165053	intron-variant	TFG	GRCh38.p7	3:100745878	TAGAATGGCAGAGTT[G/T]AGTAGTTGCAACAGA	10342
rs72928680	snp	A/C	0.0622301	0.165053	intron-variant	TFG	GRCh38.p7	3:100745920	CCCACAAAGCCTAAA[A/C]TATTTACTATCTGGC	10342
rs72928681	snp	A/C	0.0573587	0.15934	intron-variant	TFG	GRCh38.p7	3:100746086	TAATTGTATAAAATA[A/C]ATAGAACTTAAGTTT	10342
rs72928981	snp	A/G	0.0622301	0.165053	intron-variant	TFG	GRCh38.p7	3:100717576	TTGGTTTCTTTCATC[A/G]GTGTTTTTTTTTTTT	10342
rs72928991	snp	C/G	0.0368353	0.130617	intron-variant	TFG	GRCh38.p7	3:100719515	CTGAAAGAATTTACT[C/G]TCTATCCATTCATTA	10342
rs72928994	snp	C/T	0.0123036	0.0774623	intron-variant	TFG	GRCh38.p7	3:100720814	ATCTTAATAGATATG[C/T]AAGGCAGAACTCTTA	10342
rs72928997	snp	A/G	0.0352966	0.128072	intron-variant	TFG	GRCh38.p7	3:100721012	CTATTGATTTAATTT[A/G]TATCTATTTCATCTC	10342
rs72929000	snp	C/T	0.0622301	0.165053	intron-variant	TFG	GRCh38.p7	3:100721227	TTACAAATGTGTTTT[C/T]TGAATTCTGTAACTC	10342
rs72930703	snp	G/T	0.0622301	0.165053	intron-variant	TFG	GRCh38.p7	3:100723015	AAAAGTCAAGGAAGC[G/T]TAACTCTTAAACCTT	10342
rs72930705	snp	A/G	0.0221141	0.102801	intron-variant	TFG	GRCh38.p7	3:100723814	TCTTGTACATCTAGC[A/G]GTTAGGGAGAAATAC	10342
rs72930713	snp	A/C	0.0622301	0.165053	intron-variant	TFG	GRCh38.p7	3:100726466	TCTAGGCATTCCTCA[A/C]TCTAATCAAGCTGAC	10342
rs72930714	snp	C/T	0.0221141	0.102801	intron-variant	TFG	GRCh38.p7	3:100726852	GCTCTGCATTGGATG[C/T]TCTCAGGAAGTAGAG	10342
rs72930716	snp	A/T	0.0618563	0.164627	intron-variant	TFG	GRCh38.p7	3:100727804	CAGTCATGATGTAGA[A/T]AAGTTCTGCATATAT	10342
rs72930720	snp	C/T	0.0126979	0.078662	intron-variant	TFG	GRCh38.p7	3:100729254	AATTGAAAATCATTT[C/T]ATGAATAATTACATA	10342
rs72930730	snp	A/G	0.0622301	0.165053	intron-variant	TFG	GRCh38.p7	3:100730935	GGGATTAGAGGAAGG[A/G]AGTTGGTAGGGAAGA	10342
rs72930734	snp	A/T	0.0573587	0.15934	intron-variant	TFG	GRCh38.p7	3:100732327	GCCCTCTTCTCCCTG[A/T]TACTAGAAGGAAAAA	10342
rs73861203	snp	A/G	0.00478085	0.0486577	intron-variant	TFG	GRCh38.p7	3:100737735	TTGGAATAGAATCCT[A/G]TCATCCTGTGGTGAT	10342
rs73864125	snp	A/G	0.0166325	0.0896639	intron-variant	TFG	GRCh38.p7	3:100718305	GGCTTTCTCTTAACT[A/G]CTGTTTAGGGCAAAG	10342
rs74551414	snp	A/G	0.178465	0.239547	intron-variant	TFG	GRCh38.p7	3:100746391	CTTGTCAAAGCACAT[A/G]CAGCCATTCAGTGGA	10342
rs74592983	snp	C/T	0.5	0	intron-variant	TFG	GRCh38.p7	3:100743815	TGTCTTTTTTTTTTT[C/T]TCACTTCAGCAGTAA	10342
rs74732564	snp	C/T	0.030278	0.119257	intron-variant	TFG	GRCh38.p7	3:100720628	GAGCCCACCACTTAA[C/T]CTCCTGCTGTGCTGC	10342
rs74745511	snp	A/G	0.0182019	0.0936463	intron-variant	TFG	GRCh38.p7	3:100729928	CCTAGTTGCACTTCT[A/G]TTTCAGAACATAATG	10342
rs74764942	snp	A/T	0.5	0	intron-variant	TFG	GRCh38.p7	3:100746508	TAGATGTCCTATGTA[A/T]TAAAAAAAAAACTCA	10342
rs74797541	snp	A/G	0.030278	0.119257	intron-variant	TFG	GRCh38.p7	3:100735787	GTGGCTCCATATGTA[A/G]GTTAGAGTGCTAGGC	10342
rs74882965	snp	G/T			intron-variant	TFG	GRCh38.p7	3:100726845	GAGCTTTGCTCTGCA[G/T]TGGATGCTCTCAGGA	10342
rs74895058	snp	A/G	0.0283406	0.115616	intron-variant	TFG	GRCh38.p7	3:100733770	GTTGATCTAGCAGGG[A/G]GTTGATTTGTATGGA	10342
rs75064040	snp	A/G	0.137867	0.223442	intron-variant	TFG	GRCh38.p7	3:100726684	ACACACCTGTAGTTG[A/G]ATGAAGTTGGGTTTA	10342
rs75110350	snp	A/G	0.0138799	0.0821421	intron-variant	TFG	GRCh38.p7	3:100742271	TTTAAGTGAGATGAC[A/G]TATGAGGAAATCAGT	10342
rs75155854	snp	A/T	0.5	0	intron-variant	TFG	GRCh38.p7	3:100729320	TTAGTAATGTTCATT[A/T]AAAATGGTATGTTGT	10342
rs75172826	snp	C/T	0.030278	0.119257	intron-variant	TFG	GRCh38.p7	3:100731138	AAGATACATTTTGTA[C/T]TGATTACAGGGGTGA	10342
rs75195575	snp	A/G	0.0166325	0.0896639	intron-variant	TFG	GRCh38.p7	3:100746917	AGGATAGGAGAACTT[A/G]TATGACATTCAGAAT	10342
rs75268146	snp	C/T	0.0622301	0.165053	upstream-variant-2KB	TFG	GRCh38.p7	3:100709217	CAACTCTCAAAAAGT[C/T]TAGAACAGCGCACTA	10342
rs75342836	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100745160	GTAGATGATTCTGCA[A/G]TAACTTGTAGTATAA	10342
rs75658281	snp	A/G	0.00358779	0.0422022	intron-variant	TFG	GRCh38.p7	3:100743064	TATATTGTTTTGTTC[A/G]TGGGATAATATATGC	10342
rs75682335	snp	G/T	0.00358779	0.0422022	upstream-variant-2KB	TFG	GRCh38.p7	3:100708598	GACCATCTGTGCATC[G/T]TCTTGTAAAACTCAG	10342
rs75759315	snp	A/C	0.00279162	0.0372561	intron-variant	TFG	GRCh38.p7	3:100737165	TGTTAAGATTAGTAG[A/C]CTTTTATAATTTTGT	10342
rs75776618	snp	G/T	0.021333	0.101051	intron-variant	TFG	GRCh38.p7	3:100733773	GATCTAGCAGGGAGT[G/T]GATTTGTATGGACTT	10342
rs75787011	snp	G/T	0.5	0	intron-variant	TFG	GRCh38.p7	3:100711116	CAATTTTTTTTTTTT[G/T]TTGAGACGGAGTCTG	10342
rs75884251	snp	A/C/G	0.021333	0.101051	intron-variant	TFG	GRCh38.p7	3:100741257	TCATAGGAGATGAGA[A/C/G]CTCCATGGATGTTCT	10342
rs76055782	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100731104	TTATATTCGGTTTAG[C/T]ACTTAACATTTTTTT	10342
rs76071304	snp	A/G	0.0267878	0.112589	intron-variant	TFG	GRCh38.p7	3:100722176	AAACAAAACGAGAAC[A/G]TAAGAGCAAGATGCT	10342
rs76381753	snp	C/T	0.0256215	0.110247	intron-variant	TFG	GRCh38.p7	3:100735864	AGAGTGCAGAGTCTT[C/T]AAGAGGGAAAGTGAG	10342
rs76475971	snp	A/C	0.5	0	intron-variant	TFG	GRCh38.p7	3:100741178	CTTATTTAAAAAAAA[A/C]CAAAGCTGTAGAACC	10342
rs76613240	snp	C/T	0.138546	0.223781	downstream-variant-500B	TFG, ABI3BP	GRCh38.p7	3:100749160	TTTGGTAATCGTTGG[C/T]TTAAAATGAACTTTA	10342
rs76698104	snp	A/G	0.00398564	0.0444627	intron-variant	TFG	GRCh38.p7	3:100732361	AAAAAAAATAAAGGA[A/G]TTAAAATGATCTGTA	10342
rs76786969	snp	C/G	0.0399052	0.1355	intron-variant	TFG	GRCh38.p7	3:100727340	GATTGTATTGAACTT[C/G]ATAGCTATGCAGGGA	10342
rs76868158	snp	A/G	0.0256215	0.110247	intron-variant	TFG	GRCh38.p7	3:100733326	GGTTGGGTGATTTCT[A/G]TTGAACTCTTCAAGG	10342
rs76892252	snp	G/T	0.0126979	0.078662	utr-variant-3-prime	TFG	GRCh38.p7	3:100748803	ACTTGACTTTCTAGC[G/T]TCCCTTGTCCGGAGG	10342
rs77118429	snp	A/G	8.25471e-05	0.00642392	missense	TFG	GRCh38.p7	3:100728742	GACCCCTTGAATCAA[A/G]TCAGGTGAAATATCT	10342
rs77240709	snp	A/T	0.5	0	intron-variant	TFG	GRCh38.p7	3:100719968	CTTTTTTTTTTTTAA[A/T]TTCCAGATGGAGATC	10342
rs77500037	snp	A/T	0.0372196	0.131242	intron-variant	TFG	GRCh38.p7	3:100715933	GAGTACTTTTTTTTT[A/T]AAATTTTGTTTTAAT	10342
rs77524401	snp	A/C	0.0622301	0.165053	intron-variant	TFG	GRCh38.p7	3:100733730	GTGACTTGGACTTAT[A/C]TTCTTTTGAGGATTT	10342
rs77872365	snp	A/G	0.00358779	0.0422022	intron-variant	TFG	GRCh38.p7	3:100725923	GATACATTATTATGT[A/G]TGCTAGGGTTCTCCA	10342
rs77976480	snp	G/T	0.0622301	0.165053	intron-variant	TFG	GRCh38.p7	3:100735007	AAATATTACAAACAT[G/T]GAATGAATATTAACT	10342
rs78081928	snp	C/T	0.00557542	0.0525036	intron-variant	TFG	GRCh38.p7	3:100719918	CTAGTTTACTGCTTA[C/T]ACAAATCTGAAAATT	10342
rs78201157	snp	A/G	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100730502	ATGATAAGATGATAT[A/G]AGAATAATACAATCT	10342
rs78235415	snp	A/G	0.137867	0.223442	intron-variant	TFG	GRCh38.p7	3:100722192	TAAGAGCAAGATGCT[A/G]TTGTATTATGGAAAA	10342
rs78613988	snp	A/G	0.0256215	0.110247	intron-variant	TFG	GRCh38.p7	3:100722376	AAAGCACAAAAACAC[A/G]GGCAAAAGAGAAGTT	10342
rs78834500	snp	A/G	0.00358779	0.0422022	intron-variant	TFG	GRCh38.p7	3:100719360	CTTTTGAGACACACA[A/G]TTGGTATGCCAATTA	10342
rs78836077	snp	G/T	0.00398564	0.0444627	intron-variant	TFG	GRCh38.p7	3:100723749	AGAGAAATCAATAAA[G/T]TTACAATTATGGGAG	10342
rs79009614	snp	G/T	0.5	0	intron-variant	TFG	GRCh38.p7	3:100715740	AATTTTTTTTTTTTT[G/T]GAGACAGGGTCTCAC	10342
rs79126015	snp	G/T	0.0217236	0.101931	intron-variant	TFG	GRCh38.p7	3:100729555	TTCTTCTTTTAAGAT[G/T]CTTAGATGTTGCATT	10342
rs79254103	snp	C/T	0.0193772	0.0965046	intron-variant	TFG	GRCh38.p7	3:100745721	GTCTAAATTCTATTT[C/T]ATAGAGTTTTGTGGT	10342
rs79280650	in-del	-/TT			intron-variant	TFG	GRCh38.p7	3:100747352	CAATCCTTTTTTTTT[-/TT]AATGCAGGGTTGTAC	10342
rs79323767	snp	C/T	0.0256215	0.110247	intron-variant	TFG	GRCh38.p7	3:100748001	CTTGGTCTTGAAATA[C/T]TATGTGATGGAATCT	10342
rs79401794	snp	A/G	0.0023933	0.0345097	intron-variant	TFG	GRCh38.p7	3:100734641	TTTAGTTGTTACCTG[A/G]GAGAGAGTTTATCTG	10342
rs79456971	snp	C/T	0.00119737	0.0244387	intron-variant	TFG	GRCh38.p7	3:100721211	GATCTGCTAGATAAA[C/T]TTACAAATGTGTTTT	10342
rs79468618	snp	A/G	0.0622301	0.165053	intron-variant	TFG	GRCh38.p7	3:100737250	TTTTCTTCTGAAATA[A/G]TCTGTCCTTGGATAT	10342
rs79588165	snp	C/T	0	0	intron-variant	TFG	GRCh38.p7	3:100743814	ATGTCTTTTTTTTTT[C/T]CTCACTTCAGCAGTA	10342
rs79615414	snp	A/C	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100723747	AAAGAGAAATCAATA[A/C]ATTTACAATTATGGG	10342
rs79631225	snp	A/C/T	0	0	intron-variant	TFG	GRCh38.p7	3:100719965	AACCTTTTTTTTTTT[A/C/T]AAATTCCAGATGGAG	10342
rs79701142	snp	A/G	0.0221141	0.102801	intron-variant, upstream-variant-2KB, utr-variant-5-prime	TFG	GRCh38.p7	3:100710295	TTTGCTGGACACTAC[A/G]GTAAGTATTTTGGAT	10342
rs79701652	snp	A/G	0.030278	0.119257	intron-variant	TFG	GRCh38.p7	3:100729088	TAGACCTACTGGAGC[A/G]TAGCACCTGGAAATC	10342
rs79708960	snp	C/T	0.137867	0.223442	intron-variant, utr-variant-5-prime	TFG	GRCh38.p7	3:100711051	AGTCAATAGGAAACA[C/T]AAAAAGTGAATTTGC	10342
rs79791526	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100712692	AATCGTTTACTTCCT[A/G]CCATCAAGTGGAAAA	10342
rs79809822	snp	G/T	0.5	0	intron-variant	TFG	GRCh38.p7	3:100717592	GTGTTTTTTTTTTTT[G/T]TTGTAGAGGTTTTTC	10342
rs79846896	snp	A/C	0.00993419	0.0697739	intron-variant	TFG	GRCh38.p7	3:100712762	TAAGTGCTTTGAAGA[A/C]AAATAAAGCAGGATA	10342
rs79976450	in-del	-/GT			intron-variant	TFG	GRCh38.p7	3:100717595	TTTTTTTTTTTTTTT[-/GT]AGAGGTTTTTCATCT	10342
rs80232856	snp	C/G	0.0182019	0.0936463	intron-variant, upstream-variant-2KB	TFG	GRCh38.p7	3:100710521	CTTGGCTTAGTATTT[C/G]TTGAAGGAAACTGCT	10342
rs80254166	snp	C/G	0.0573587	0.15934	intron-variant	TFG	GRCh38.p7	3:100713001	GATTTTATAGGTCTT[C/G]CTTTTTGGGATGAGA	10342
rs111356679	snp	C/G	0.0026671	0.0364203	missense	TFG	GRCh38.p7	3:100748388	ATGGCTCCAAGCCAA[C/G]CTGGGGCCTATCAAC	10342
rs111492604	snp	A/G	0.5	0	intron-variant	TFG	GRCh38.p7	3:100724518	GAAATTGGGCCAACT[A/G]TTTTACCAAATATCT	10342
rs111540048	snp	A/G	0.0182019	0.0936463	intron-variant, upstream-variant-2KB, utr-variant-5-prime	TFG	GRCh38.p7	3:100709454	CACGCGCAATAAGGA[A/G]GGGCGAAAGGACATT	10342
rs111616660	snp	A/G	0.0221141	0.102801	intron-variant	TFG	GRCh38.p7	3:100725061	GGCACCTGCCACCAC[A/G]CCCGGCTAATTTGTT	10342
rs111734696	snp	A/T			utr-variant-3-prime, downstream-variant-500B	TFG, ABI3BP	GRCh38.p7	3:100748965	AGATGATTGAATCCA[A/T]TAGTGGTCTTGAAAT	10342
rs111983454	snp	A/C			intron-variant, upstream-variant-2KB	TFG	GRCh38.p7	3:100709831	GCTGGGGTCGGAGGC[A/C]CTGTGGGAAGGGGCT	10342
rs112080920	snp	A/G	0.0622301	0.165053	intron-variant, upstream-variant-2KB	TFG	GRCh38.p7	3:100710881	ACCAGAATTCTGTAT[A/G]TGAAGTAATGTTGGG	10342
rs112148271	snp	A/G	0.0573587	0.15934	intron-variant	TFG	GRCh38.p7	3:100725286	ATAAAAGGATTATAA[A/G]TGTAACTAAAATACC	10342
rs112446290	snp	C/T	0.0622301	0.165053	intron-variant	TFG	GRCh38.p7	3:100711334	TCTTGGACTCCTGAC[C/T]TCGTGATCTGCCCGC	10342
rs112587963	snp	G/T	0.0225045	0.103662	intron-variant	TFG	GRCh38.p7	3:100735022	GGAATGAATATTAAC[G/T]GTAATAAATTACATA	10342
rs112647894	snp	A/C/G	5.07378e-05	0.0050365	utr-variant-5-prime	TFG	GRCh38.p7	3:100713683	AACATCCTGGAGTCC[A/C/G]CCATGAACGGACAGT	10342
rs112687896	snp	G/T			intron-variant	TFG	GRCh38.p7	3:100739461	GTTACAGGAAGACTA[G/T]GTGATGTTGCCAGAA	10342
rs112746341	snp	C/T	0	0	intron-variant	TFG	GRCh38.p7	3:100733028	GCAGTATTCGAATTA[C/T]ATTTGATTTGTCTTA	10342
rs112759386	snp	C/T	0.0126979	0.078662	utr-variant-5-prime, upstream-variant-2KB	TFG	GRCh38.p7	3:100709399	CGGGACCCAGCCAGC[C/T]CTGCGCCTCGCGCCG	10342
rs112892780	snp	C/G	0.5	0	intron-variant	TFG	GRCh38.p7	3:100726771	AAGTATGTTAGAAAA[C/G]TATTTTTTTTTGGGC	10342
rs112902891	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100715891	ATTCAGATTTTTAAC[C/T]TTTTTTTTTTTTTAG	10342
rs113216779	snp	C/T	0.00159617	0.0282053	intron-variant	TFG	GRCh38.p7	3:100716876	CAGATCATTTGCCGA[C/T]TTTAAAATCGGATTG	10342
rs113246505	snp	A/C			intron-variant	TFG	GRCh38.p7	3:100725683	GCCTGTAATCCAGCC[A/C]CTTGGGAGGCTGAGA	10342
rs113291340	snp	C/T	0.5	0	intron-variant	TFG	GRCh38.p7	3:100717263	TTTTTATGTCAGTTC[C/T]GTTGGTCTGTGGGTC	10342
rs113426329	snp	C/T	0.5	0	intron-variant, upstream-variant-2KB, utr-variant-5-prime	TFG	GRCh38.p7	3:100709490	TTTTCTTGCTCCCGC[C/T]TCTGTTCTTCCCCCA	10342
rs113505805	snp	A/T	0.5	0	intron-variant	TFG	GRCh38.p7	3:100745355	AGGTGATGTTATTTA[A/T]ATAAGAGCTCAATTA	10342
rs113590781	snp	A/G	0.00920632	0.0672191	utr-variant-3-prime	TFG	GRCh38.p7	3:100748569	ATGTAGCTGCTAGCT[A/G]TTGGCCTCCCAAAAG	10342
rs113630353	snp	G/T	0.0622301	0.165053	intron-variant	TFG	GRCh38.p7	3:100725672	TAGTGGTGCGTGCCT[G/T]TAATCCAGCCACTTG	10342
rs113702248	snp	A/G	0.0260105	0.111035	intron-variant	TFG	GRCh38.p7	3:100723439	ACACAGAAATTGACT[A/G]CATATATCGGTTAAA	10342
rs113740006	snp	A/T	0.0221141	0.102801	intron-variant	TFG	GRCh38.p7	3:100729347	TTGTAAATTTGAAAC[A/T]CAGTTTTTAATAATA	10342
rs113903462	snp	A/C			intron-variant	TFG	GRCh38.p7	3:100725625	CTACCAAAAATACAA[A/C]AAAAAAAAAAAAAAA	10342
rs113982085	snp	A/T			utr-variant-3-prime, downstream-variant-500B	TFG, ABI3BP	GRCh38.p7	3:100748966	GATGATTGAATCCAT[A/T]AGTGGTCTTGAAATT	10342
rs114055260	snp	C/G/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100718311	CTCTTAACTACTGTT[C/G/T]AGGGCAAAGGTCAGC	10342
rs114124529	snp	A/G	0.0252325	0.109451	intron-variant, upstream-variant-2KB, utr-variant-5-prime	TFG	GRCh38.p7	3:100709512	CTTCCCCCACCTGCC[A/G]CGTACAGAGCCCAAG	10342
rs114182138	snp	C/T	0.00517822	0.0506191	intron-variant	TFG	GRCh38.p7	3:100731875	TATTTTGATGCAGAT[C/T]CCATATACATCATTT	10342
rs114195574	snp	A/G	0.0142736	0.0832652	intron-variant	TFG	GRCh38.p7	3:100728947	AGTAGGAGAAGGATG[A/G]CATCCCCAATGTCAC	10342
rs114232641	snp	C/T	0.00517822	0.0506191	intron-variant	TFG	GRCh38.p7	3:100730819	AAGTAGTAGGACGTA[C/T]AGTATGTTTCCTGAT	10342
rs114259024	snp	G/T	0.0138799	0.0821421	intron-variant	TFG	GRCh38.p7	3:100715311	TGACATTGGCAAGCA[G/T]ATGAGTGAAGACAGA	10342
rs114269876	snp	C/G	0.0622301	0.165053	intron-variant	TFG	GRCh38.p7	3:100736985	CAGTGGTGACCCTTG[C/G]AGGGGAGGATAGTGA	10342
rs114298311	snp	A/G	0.0023933	0.0345097	intron-variant	TFG	GRCh38.p7	3:100727613	CTGAGTGGTGACAGT[A/G]TTTGTTGCTGAATGA	10342
rs114305882	snp	A/T	0.00517822	0.0506191	intron-variant	TFG	GRCh38.p7	3:100717803	TTTTAGGTTTTTGTT[A/T]ATATAAGATTATGTC	10342
rs114425837	snp	C/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100721458	AAAAAGAATATTTTA[C/G]AAAAGTCTACCTTGA	10342
rs114535253	snp	A/G	0.00557542	0.0525036	intron-variant	TFG	GRCh38.p7	3:100722364	AAATTACAGAGTAAA[A/G]CACAAAAACACAGGC	10342
rs114606395	snp	A/T	0.00478085	0.0486577	intron-variant	TFG	GRCh38.p7	3:100740461	GAGTGAGGTAGAAGA[A/T]AACCTTTTATAGCCT	10342
rs114652332	snp	C/T	0.0138799	0.0821421	upstream-variant-2KB	TFG	GRCh38.p7	3:100708347	TCTTCCACCACGTGG[C/T]TCTGCTGGAGTCTCT	10342
rs114658094	snp	A/T	0.00597247	0.0543191	intron-variant	TFG	GRCh38.p7	3:100724664	AAATGCAAACCAGTG[A/T]CACGTATGAACATAG	10342
rs114709278	snp	C/T	0.00517822	0.0506191	intron-variant	TFG	GRCh38.p7	3:100745165	TGATTCTGCAGTAAC[C/T]TGTAGTATAAAAAGT	10342
rs114737517	snp	C/T	0.00279162	0.0372561	intron-variant	TFG	GRCh38.p7	3:100728449	TTAAAAAGTAGAGCT[C/T]GGATTTTCCTACCAA	10342
rs114798796	snp	A/G	0.0236746	0.106192	intron-variant	TFG	GRCh38.p7	3:100740691	TGCAGAAGCCGTTGA[A/G]GGTCATGATAGAGGT	10342
rs115001931	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100724920	AGGGAATTCTTTTTT[A/G]TGAGGCAGAGTCTCT	10342
rs115063872	snp	C/T	0.00199481	0.0315187	intron-variant	TFG	GRCh38.p7	3:100730122	AGAATTCATAGATGC[C/T]GACACAACATTTGCA	10342
rs115091367	snp	A/G	0.00755907	0.0610114	intron-variant	TFG	GRCh38.p7	3:100721587	TGGGTTTAAATTTAA[A/G]CTATCCATGTAGTTT	10342
rs115119283	snp	G/T	0.0023933	0.0345097	intron-variant	TFG	GRCh38.p7	3:100744036	ATAAACCAATAAATC[G/T]TTGCTTGAAAATCAC	10342
rs115126937	snp	C/T	0.0023933	0.0345097	intron-variant	TFG	GRCh38.p7	3:100718847	ACAGGTGTGAGCCAC[C/T]GCACTTGGCCAAAAA	10342
rs115129534	snp	G/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100734164	CTCTTCATGGCCTTA[G/T]CAGAGTTTTTAATTT	10342
rs115191986	snp	A/G	0.0240643	0.107019	intron-variant	TFG	GRCh38.p7	3:100723058	GATTGGGAAGCACCA[A/G]TGAAATTTATGTGTA	10342
rs115462724	snp	A/C	0.00636936	0.0560724	intron-variant	TFG	GRCh38.p7	3:100747577	TATGGTATGCTTTTT[A/C]TGTGTTATGCTGTAC	10342
rs115469584	snp	A/G	0.00755907	0.0610114	intron-variant	TFG	GRCh38.p7	3:100742273	TAAGTGAGATGACGT[A/G]TGAGGAAATCAGTTC	10342
rs115506116	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100744236	TTATTAAATAGTGCA[A/G]TGAAGAACCATTTAG	10342
rs115518854	snp	A/G	0.030278	0.119257	intron-variant	TFG	GRCh38.p7	3:100715983	ATATTTATGGGGTAC[A/G]TAGTAATGTTTCATT	10342
rs115588147	snp	G/T	0.0182019	0.0936463	intron-variant	TFG	GRCh38.p7	3:100712369	CAGAGAAGTGTGGTG[G/T]TAATGAAATAACAGA	10342
rs115622078	snp	A/C	0.0107246	0.0724382	intron-variant	TFG	GRCh38.p7	3:100746519	TGTATTAAAAAAAAA[A/C]CTCACATAATTTCCA	10342
rs115656907	snp	A/G	0.0622301	0.165053	intron-variant	TFG	GRCh38.p7	3:100736986	AGTGGTGACCCTTGG[A/G]GGGGAGGATAGTGAA	10342
rs115659798	snp	G/T	0.00557542	0.0525036	intron-variant	TFG	GRCh38.p7	3:100731205	AAAGTGATAATCATT[G/T]TCCCTTAATTGAGTA	10342
rs115795124	snp	A/G	0.00914312	0.0669923	intron-variant	TFG	GRCh38.p7	3:100741862	TCAGTACAGGAACAT[A/G]CTCTACAGGTTTGTA	10342
rs115821936	snp	A/G	0.00874735	0.0655527	intron-variant	TFG	GRCh38.p7	3:100741255	TATCATAGGAGATGA[A/G]AGCTCCATGGATGTT	10342
rs115858291	snp	C/T	0.0123036	0.0774623	intron-variant	TFG	GRCh38.p7	3:100714863	CTTTATGGAAATAGG[C/T]TTTGAATGAAAAATG	10342
rs115861305	snp	A/T	0.0138799	0.0821421	intron-variant	TFG	GRCh38.p7	3:100719116	AAAACAGTTATAAAA[A/T]TCTCAGTTTTGTCAT	10342
rs115896544	snp	C/T	0.0100045	0.0700155	intron-variant	TFG	GRCh38.p7	3:100732499	TTGTTTATTCCTCTA[C/T]TTTTACAGATACTGT	10342
rs116111855	snp	G/T	0.0023933	0.0345097	intron-variant	TFG	GRCh38.p7	3:100733161	AGTACCTATATTGTT[G/T]TATTCTGTTTAACTT	10342
rs116194209	snp	A/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100721621	AACTCCCAAGCCCAG[A/T]TGTTACCATTTTAGA	10342
rs116217929	snp	A/G	0.00517822	0.0506191	intron-variant, upstream-variant-2KB	TFG	GRCh38.p7	3:100710334	TCATTTAATCATCAC[A/G]AGGATTCCTCCAAAT	10342
rs116251760	snp	A/C/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100743424	TATGAAGTACAATCC[A/C/G]GGATTAAGGTGGCAT	10342
rs116296871	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100744091	CAGAAAAATAAAAAG[C/T]AAAAAGAAAAATCAT	10342
rs116331452	snp	C/T	0.00517822	0.0506191	intron-variant	TFG	GRCh38.p7	3:100729971	ATACTATAATGAGAT[C/T]CTCTTGGTCACTTTA	10342
rs116468556	snp	A/G	0.030278	0.119257	intron-variant	TFG	GRCh38.p7	3:100735280	ACTGTGCCTAATACT[A/G]TGGTAAGTTCTGGGG	10342
rs116604834	snp	G/T	0.00517822	0.0506191	intron-variant	TFG	GRCh38.p7	3:100745609	TATTTTTTACAGTTA[G/T]GTCAGAGAGTTTGTG	10342
rs116622528	snp	C/T	0.00517822	0.0506191	upstream-variant-2KB	TFG	GRCh38.p7	3:100708315	CTGTACCTCATTTCC[C/T]TTTTTTTGTCTATAA	10342
rs116630229	snp	A/G	0.0166325	0.0896639	intron-variant	TFG	GRCh38.p7	3:100742620	TAACCTAACATACAC[A/G]TCTTTGGGATGTGGG	10342
rs116650206	snp	A/T	0.00914312	0.0669923	upstream-variant-2KB	TFG	GRCh38.p7	3:100708307	GCCAATTTCTGTACC[A/T]CATTTCCCTTTTTTT	10342
rs116712784	snp	A/G	0.00517822	0.0506191	intron-variant, upstream-variant-2KB	TFG	GRCh38.p7	3:100710864	TGGAAGAGAAAATGA[A/G]TACCAGAATTCTGTA	10342
rs116722727	snp	A/G	0.0111196	0.0737302	intron-variant	TFG	GRCh38.p7	3:100715438	CTTTGCTAAGATGCA[A/G]ATGGGTTGGGAAGTA	10342
rs116776998	snp	A/G	0.030278	0.119257	intron-variant	TFG	GRCh38.p7	3:100732924	ACCCTCCCCCTTAAA[A/G]AATAAGCACTGTTGG	10342
rs116848500	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100726298	TTATCCTACCTTCTT[C/T]TGCCTGTTTTGTGAT	10342
rs116891811	snp	G/T	0.00755907	0.0610114	intron-variant	TFG	GRCh38.p7	3:100733758	TTTTCTGTTATTGTT[G/T]ATCTAGCAGGGAGTT	10342
rs117485319	snp	G/T	0.185155	0.241444	intron-variant	TFG	GRCh38.p7	3:100711153	TCGCCCAGGCTGTAG[G/T]GCAGTGGCGTGATCC	10342
rs117615600	snp	A/G	0.00557542	0.0525036	intron-variant	TFG	GRCh38.p7	3:100726118	GAAGCTGATAGTGCA[A/G]CCTTTGTCTGTTGCC	10342
rs117690900	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100728625	TTGTTTTTTTAAAGG[A/G]ATTGTATTTATTTTT	10342
rs118050713	snp	A/G	0.00159617	0.0282053	intron-variant	TFG	GRCh38.p7	3:100730808	GCTAATGGAGCAAGT[A/G]GTAGGACGTATAGTA	10342
rs137920624	snp	A/C	0.0103295	0.0711199	intron-variant	TFG	GRCh38.p7	3:100723441	ACAGAAATTGACTAC[A/C]TATATCGGTTAAAAT	10342
rs137969865	snp	A/T	0.00279162	0.0372561	intron-variant	TFG	GRCh38.p7	3:100713261	ATTTTCTTGGCAGTT[A/T]GGATGTAAGGTTTGA	10342
rs138036078	snp	C/T	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100717110	CATGAAATCTTTTCC[C/T]GACCTATTAAAGAGG	10342
rs138185005	snp	C/T	0.000165333	0.00909061	missense	TFG	GRCh38.p7	3:100748473	GGCCTAATCCTTATG[C/T]GCGTAACCGTCCTCC	10342
rs138202541	snp	A/C	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100741885	GGTTTGTAGACTGCT[A/C]TGTACCATATAGCCT	10342
rs138238536	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, utr-variant-5-prime	TFG	GRCh38.p7	3:100710181	TTGGGGTCATAGAAT[C/G]GGAGCCTAGTTCCTT	10342
rs138245563	snp	A/G	0.0123036	0.0774623	intron-variant	TFG	GRCh38.p7	3:100730480	TGTGTCCTGTCTGAC[A/G]TATCTGATGATAAGA	10342
rs138595404	snp	A/G	0.00279162	0.0372561	intron-variant	TFG	GRCh38.p7	3:100726944	CTAAATCTTATCTGG[A/G]AGGTGAGAGGAATGA	10342
rs138624638	snp	C/T	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100722917	GAAAGATGCAAGAAG[C/T]AATGTGAGCAGATAA	10342
rs138632976	snp	G/T	0.00636936	0.0560724	intron-variant	TFG	GRCh38.p7	3:100712259	ATATTCATATAATAG[G/T]ATTCATGAAAACTTT	10342
rs138780648	snp	A/G	0.00358779	0.0422022	intron-variant, upstream-variant-2KB, utr-variant-5-prime	TFG	GRCh38.p7	3:100709526	CACGTACAGAGCCCA[A/G]GTTCTCGCTAGGCTT	10342
rs138858804	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100734708	TGTACAGTCCATTTT[A/G]TATTTCTTAGAGACT	10342
rs138901438	in-del	-/T			intron-variant, upstream-variant-2KB, utr-variant-5-prime	TFG	GRCh38.p7	3:100710266	ATGATTCTAGCTAAC[-/T]TTTAAGAGTTTGCTT	10342
rs138901713	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100727216	GCAACACTAAGGCCT[A/G]TCTTACTGTACCAGA	10342
rs138912047	snp	C/T	0.00318978	0.0398085	intron-variant	TFG	GRCh38.p7	3:100737383	ATAACCTGAAAGCTC[C/T]ATATTTAAAATAGGG	10342
rs138915064	snp	C/T	0.0170251	0.090679	intron-variant	TFG	GRCh38.p7	3:100738889	GCCTAATGTATCCAA[C/T]GTGTACTCACTATTA	10342
rs138982414	snp	G/T	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100743170	TTCTTAGCTATTGAC[G/T]GCAGGTAAGTTGCTT	10342
rs139051286	snp	A/G	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100747261	TTTTGTTCATGGACT[A/G]TGTCATAAAGGTTTC	10342
rs139114111	in-del	-/TGAC	0.0622301	0.165053	intron-variant	TFG	GRCh38.p7	3:100717838	CAAACAGGGACAGTT[-/TGAC]TGCTTCCTTCCCAAT	10342
rs139169678	in-del	-/CT/CTT/T/TT	0.0919063	0.197263	intron-variant	TFG	GRCh38.p7	3:100713902	CTATTTTTTAAAGTC[-/CT/CTT/T/TT]TTTTTAAAAAAAAAA	10342
rs139186664	snp	C/T	0.00318978	0.0398085	intron-variant, upstream-variant-2KB	TFG	GRCh38.p7	3:100710717	TACCTGGTAGAGGGT[C/T]ATATTATACAAGTTA	10342
rs139253819	in-del	-/GTAA			downstream-variant-500B, utr-variant-3-prime	TFG, ABI3BP	GRCh38.p7	3:100749425	GAAGCATGTTGAAAG[-/GTAA]GTAAGTACAGGGAAA	10342
rs139267538	snp	C/G	0.030278	0.119257	intron-variant	TFG	GRCh38.p7	3:100725029	CCATCTCAGCTTCCC[C/G]AGTAGCTGGGACTAC	10342
rs139510666	snp	C/T	0.021333	0.101051	intron-variant	TFG	GRCh38.p7	3:100744990	CTATACTCATTAAAC[C/T]TTAAGTTCTTAATTC	10342
rs139543668	snp	C/G	0.000798403	0.0199641	upstream-variant-2KB	TFG	GRCh38.p7	3:100708039	CTCCAGGTCCTTTAG[C/G]AGTATCTGGTGTTAA	10342
rs139601254	snp	A/G	1.64904e-05	0.00287139	missense	TFG	GRCh38.p7	3:100736695	TATACAGGAGCTCAG[A/G]CTCAAGCAGGTCAGA	10342
rs139621969	snp	G/T	0.00517822	0.0506191	intron-variant	TFG	GRCh38.p7	3:100739053	GTGATTATTTTAAGA[G/T]CACAGCTTTAGATAA	10342
rs139751879	snp	A/G	0.00159617	0.0282053	upstream-variant-2KB	TFG	GRCh38.p7	3:100707580	TATCTCCTGCCTCAG[A/G]ATCTGACCTCTTTTT	10342
rs139766916	snp	G/T	0.021333	0.101051	intron-variant	TFG	GRCh38.p7	3:100720654	GCTGCCCAGCCCGGT[G/T]TGGTTCCTAACAGGC	10342
rs139788926	snp	C/T	0.00398564	0.0444627	intron-variant	TFG	GRCh38.p7	3:100711161	GCTGTAGTGCAGTGG[C/T]GTGATCCCCCAGCTC	10342
rs139823622	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100713477	AAGCTTATTTTATTA[C/T]CCCTACAGTAAAATA	10342
rs139973683	snp	A/C	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100715101	CTCTTAACATCTCTG[A/C]CACTGCTTAACCTAG	10342
rs140003035	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100728421	TGATTTTTATTAAAT[C/T]TAATCATTTCTATTA	10342
rs140040665	snp	A/T	0.00597247	0.0543191	intron-variant	TFG	GRCh38.p7	3:100716128	GTTATTGTTAACTGT[A/T]GTCATCCTATAGTGC	10342
rs140108086	snp	A/G	0.00358779	0.0422022	intron-variant	TFG	GRCh38.p7	3:100719426	CGGTCATAAATACAC[A/G]CTGTTTTGAATATAT	10342
rs140172180	in-del	-/T	0.0182019	0.0936463	intron-variant	TFG	GRCh38.p7	3:100714991	AGGTGGTTACCAGTG[-/T]TTTTTTACTGTGGAA	10342
rs140174542	snp	C/G	6.62153e-05	0.00575354	missense	TFG	GRCh38.p7	3:100720046	AGTAGGATACTGAAA[C/G]TGACATTATTTGGTG	10342
rs140174756	snp	G/T	0.0244538	0.107838	intron-variant	TFG	GRCh38.p7	3:100723958	TCTGGCTTCTTTAGA[G/T]ACTATTGGACAGAAT	10342
rs140327635	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100728864	CCTGAAAATGGTAAA[C/T]CCTGAATCCATTGTA	10342
rs140393115	snp	C/G	0.00398564	0.0444627	intron-variant	TFG	GRCh38.p7	3:100716733	TAATAACCATCCTAA[C/G]TGGGGTGAACCTTGT	10342
rs140466338	snp	G/T	0.000313436	0.0125148	missense	TFG	GRCh38.p7	3:100732549	TCTGCTTCTGATTCT[G/T]CTGGAAAACAGTCTA	10342
rs140529972	snp	C/G	0.00517822	0.0506191	intron-variant	TFG	GRCh38.p7	3:100735494	AGGAATTAGTATATC[C/G]TTTGTACAGATGAGG	10342
rs140534284	snp	C/T	0.00318978	0.0398085	intron-variant	TFG	GRCh38.p7	3:100741242	AAGAAGGCATTGTTA[C/T]CATAGGAGATGAGAG	10342
rs140669729	snp	A/C/G/T	0.00431113	0.0462336	synonymous-codon	TFG	GRCh38.p7	3:100736658	AGCTCACCCACCAGG[A/C/G/T]GTTCAGCCACAGCAG	10342
rs140713495	snp	C/G	0.0107246	0.0724382	upstream-variant-2KB	TFG	GRCh38.p7	3:100708680	ATGGGGTTCCTCATC[C/G]TCCACCACCCCCAGG	10342
rs140990513	snp	A/G	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100747056	CAGGGTCTTCACTCT[A/G]AGTAAAATTTAGTCT	10342
rs141024756	snp	C/G	0.00517822	0.0506191	utr-variant-5-prime, upstream-variant-2KB	TFG	GRCh38.p7	3:100709351	AAATCCCGTCATCCA[C/G]TGAGAAAGCAGGGAC	10342
rs141043777	snp	A/G	0.00199481	0.0315187	intron-variant	TFG	GRCh38.p7	3:100722544	CGGGGAGCCTTGAGC[A/G]GGGATAAGTAAAAGT	10342
rs141090139	snp	C/T	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100729788	AGTTTTTGTTTTCTA[C/T]TTTTATTTTAGTTAC	10342
rs141158265	snp	C/G	0.00517822	0.0506191	intron-variant	TFG	GRCh38.p7	3:100733613	TGGGTTCCTCTCCCC[C/G]ACACACACTCCCCCC	10342
rs141205213	snp	A/G	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100722989	TAGAAAAGCTTTTCC[A/G]TTGATACAGAAAAAG	10342
rs141295142	in-del	-/TTTA	0.0573587	0.15934	intron-variant	TFG	GRCh38.p7	3:100741138	TTACTATACTATATT[-/TTTA]AATCATTAGAGTGTA	10342
rs141367649	snp	A/G	0.00438332	0.0466095	intron-variant	TFG	GRCh38.p7	3:100737218	TGGAAAAAAAGCAGT[A/G]TATTTTAAGTCAGAC	10342
rs141412018	snp	A/G	6.59489e-05	0.00574196	synonymous-codon	TFG	GRCh38.p7	3:100736667	ACCAGGCGTTCAGCC[A/G]CAGCAGCCACCATAT	10342
rs141424854	snp	A/G	0.00517822	0.0506191	intron-variant	TFG	GRCh38.p7	3:100739507	AGAAGAACGCTAAAA[A/G]TCATCAGAGATCGGG	10342
rs141437466	snp	A/G	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100734991	GTGGGAAGGAGGGAT[A/G]AAATATTACAAACAT	10342
rs141580409	snp	C/T	0.0622301	0.165053	intron-variant, utr-variant-5-prime, upstream-variant-2KB	TFG	GRCh38.p7	3:100709800	GCTGGGAGGGCCTCG[C/T]TCGAACCGCGCGGCA	10342
rs141580665	snp	C/T	0.00557542	0.0525036	intron-variant	TFG	GRCh38.p7	3:100718698	AAGTAGCTGGAATTA[C/T]AGGCACACACCACCA	10342
rs141642300	snp	A/G	0.030278	0.119257	intron-variant	TFG	GRCh38.p7	3:100711378	AGTGCTGGGATTACA[A/G]GTGTGAGCCACCGTG	10342
rs141678323	in-del	-/A	0.0622301	0.165053	intron-variant	TFG	GRCh38.p7	3:100737095	TGATTTTTCTAATTT[-/A]AAAAAGATTTCTGAA	10342
rs141723121	snp	A/T	0.00279162	0.0372561	intron-variant	TFG	GRCh38.p7	3:100743858	CTCATAGTCTTTTGA[A/T]TAATAGGTAGTTTGA	10342
rs141786985	snp	C/T	9.89838e-05	0.00703435	synonymous-codon	TFG	GRCh38.p7	3:100736616	TCGTTCAGGAACACC[C/T]GACAGCATTGCTTCC	10342
rs141826568	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100737914	ATTTAAAAAAATTAG[C/T]CAGGTGCTATGGCAT	10342
rs141872904	in-del	-/TA	0.00517822	0.0506191	intron-variant	TFG	GRCh38.p7	3:100742794	TGAGGATCTGCTGTG[-/TA]AAAGGAATCTTGTGT	10342
rs141910988	in-del	-/TG	0.0573587	0.15934	intron-variant	TFG	GRCh38.p7	3:100742790	TATTTGAGGATCTGC[-/TG]TGTAAAAGGAATCTT	10342
rs141932112	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100731767	TTGCCAGGCTGGTCT[C/T]GAGCTCCTGACCTCA	10342
rs141995994	snp	C/G	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100726620	TGTAAATGCAAGGTT[C/G]TTAAAAGTTCTGGTA	10342
rs142048727	snp	A/G	0.0166325	0.0896639	intron-variant	TFG	GRCh38.p7	3:100713482	TATTTTATTATCCCT[A/G]CAGTAAAATAATGTT	10342
rs142052867	snp	A/T	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100739413	AAAACCAAAAGGGAT[A/T]ATGTTACTCTTTTTC	10342
rs142060861	snp	A/G	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100729182	CACAGGTCAGTTTTC[A/G]AATCCTTTTGACACA	10342
rs142325067	snp	C/T	0.00199481	0.0315187	intron-variant	TFG	GRCh38.p7	3:100711995	GTGAGAACTGGCAGA[C/T]AAAAAGCTAACTGTA	10342
rs142356585	snp	A/G	0.00279162	0.0372561	intron-variant	TFG	GRCh38.p7	3:100724755	GTGTCAAAATTGCTC[A/G]CCCAAGGAGTCTAAG	10342
rs142358942	snp	A/G/T	0.0225045	0.103662	intron-variant	TFG	GRCh38.p7	3:100716408	TGTATTCCATTGTGT[A/G/T]TATATACCATATTTT	10342
rs142461512	snp	A/C	0.00279162	0.0372561	intron-variant	TFG	GRCh38.p7	3:100713329	ACTCGAAGGAAGATA[A/C]AGAAGCCTCTAGGAG	10342
rs142528467	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100717206	CTTTTGTTCTATGTG[C/T]TCTATTGATCTATGT	10342
rs142537338	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100735856	CGGCCAAAAGAGTGC[A/G]GAGTCTTTAAGAGGG	10342
rs142835522	snp	C/T	0.00517822	0.0506191	intron-variant	TFG	GRCh38.p7	3:100738941	TGTGTATTGGAAGTC[C/T]GGGATTTGACACTGA	10342
rs142862287	snp	C/T	0.00159617	0.0282053	intron-variant	TFG	GRCh38.p7	3:100730646	GTGCTATTTAGAACC[C/T]GTGGCTTACCCTCAC	10342
rs142900885	snp	C/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100743250	AAATGTGTTTATTGC[C/G]TGTTTGCTTATTTTT	10342
rs142916668	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100745413	AAGTATGTAGGAATA[C/T]CAGAAATAGGCCATA	10342
rs142928170	snp	C/T	0.00279162	0.0372561	intron-variant	TFG	GRCh38.p7	3:100734273	GTATAGCAGCTGATA[C/T]GTATGCTCAGTCCTT	10342
rs143129431	snp	C/G	1.65636e-05	0.00287776	missense	TFG	GRCh38.p7	3:100748290	CACAGCAGTACCAGG[C/G]GAGCAATTATCCTGC	10342
rs143216354	snp	C/T	0.00517822	0.0506191	intron-variant	TFG	GRCh38.p7	3:100745031	AGTACATTGATATAA[C/T]AGGTATTAAGTTTTT	10342
rs143229558	snp	G/T	0.00358779	0.0422022	intron-variant	TFG	GRCh38.p7	3:100716530	CTCTTCAATATACTG[G/T]TTTCCTTTCCTTTAG	10342
rs143499374	snp	A/G	0.00517822	0.0506191	intron-variant	TFG	GRCh38.p7	3:100728424	TTTTTATTAAATTTA[A/G]TCATTTCTATTAAAA	10342
rs143508894	snp	C/T	0.00517822	0.0506191	intron-variant	TFG	GRCh38.p7	3:100725920	GAAGATACATTATTA[C/T]GTGTGCTAGGGTTCT	10342
rs143670310	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	TFG	GRCh38.p7	3:100707871	TGCTCAAAGGTCAAT[A/G]CAACTGTTGGAAAAT	10342
rs143795364	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100734043	GGCAGATGTCCTCAC[A/G]GTCACAGAAGTTTTT	10342
rs143855434	snp	A/G	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100740049	ATGAGGGGCCTAACA[A/G]GGTTCACACTTTGCA	10342
rs143918475	snp	C/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100745265	CTTCCCTCCACCTCT[C/G]CATTTATATGTAACA	10342
rs143933645	snp	G/T	0.00517822	0.0506191	intron-variant	TFG	GRCh38.p7	3:100739247	AATCTCTTACAATGT[G/T]TTAATAGTCCATACT	10342
rs143977554	snp	C/T			upstream-variant-2KB	TFG	GRCh38.p7	3:100708403	CCCAATTCGTGAAAT[C/T]GTTCACTGCTCAATT	10342
rs144012059	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	TFG	GRCh38.p7	3:100710736	TTATACAAGTTAGAA[A/G]CCGAGTCATTTCTGG	10342
rs144100816	snp	A/T	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100727078	TTGTCTGGAGTTTTG[A/T]CATGGTTATGGACTG	10342
rs144101732	snp	A/C	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	TFG	GRCh38.p7	3:100710352	GATTCCTCCAAATTC[A/C]GATATGGTTGTTTTC	10342
rs144108914	snp	C/T	0.0166325	0.0896639	intron-variant	TFG	GRCh38.p7	3:100735387	TTTCTGAGTAGTAGT[C/T]ACTTTTATAAGCTTT	10342
rs144193250	snp	C/T	0.00795532	0.062565	intron-variant	TFG	GRCh38.p7	3:100725060	AGGCACCTGCCACCA[C/T]GCCCGGCTAATTTGT	10342
rs144232206	in-del	-/GT	0.021333	0.101051	intron-variant	TFG	GRCh38.p7	3:100735875	TCTTTAAGAGGGAAA[-/GT]GAGAGCTATTCAGAA	10342
rs144233495	snp	C/T	0.0166325	0.0896639	intron-variant	TFG	GRCh38.p7	3:100728293	TTATTTTAAGAATAG[C/T]GTGAAATAAAATGAG	10342
rs144325884	snp	A/G/T	0.00517997	0.0506535	intron-variant	TFG	GRCh38.p7	3:100732930	CCCCTTAAAGAATAA[A/G/T]CACTGTTGGGTTCAA	10342
rs144326585	in-del	-/A	0.021333	0.101051	intron-variant	TFG	GRCh38.p7	3:100744043	ATAAATCTTTGCTTG[-/A]AAAATCACAGGTATG	10342
rs144368144	snp	A/G	4.94645e-05	0.00497291	missense	TFG	GRCh38.p7	3:100736659	GCTCACCCACCAGGC[A/G]TTCAGCCACAGCAGC	10342
rs144387996	snp	A/G	0.0023933	0.0345097	intron-variant	TFG	GRCh38.p7	3:100735508	CCTTTGTACAGATGA[A/G]GAAACTGAGGCACAG	10342
rs144391999	in-del	-/GTGATTTTCCTTCTCAGATAAAAGGTATAGTTGATTTGA			downstream-variant-500B	TFG, ABI3BP	GRCh38.p7	3:100749224	AAACAAACAGTAGAT[lengthTooLong]ATAATGGGGGTTGGT	10342
rs144544617	snp	C/T	0.00318978	0.0398085	intron-variant	TFG	GRCh38.p7	3:100713242	TAAAGGCAGTGGCAA[C/T]CATATTTTCTTGGCA	10342
rs144643993	snp	A/G	0.0111196	0.0737302	intron-variant	TFG	GRCh38.p7	3:100731800	TGATCTACCCACCTC[A/G]GCCTCTCAAAGTGCT	10342
rs144700412	snp	C/T	0.00318978	0.0398085	intron-variant	TFG	GRCh38.p7	3:100717342	GGTCAGTAAGTGTGA[C/T]ACCTTCAGCTTTGTT	10342
rs144750357	snp	A/G	0.0119091	0.0762411	intron-variant	TFG	GRCh38.p7	3:100727729	CAACTAGAGATTACC[A/G]AGTAATCTCTGGCAT	10342
rs144763564	snp	A/C	0.0023933	0.0345097	intron-variant	TFG	GRCh38.p7	3:100722742	GCAAACAGTAAAGAA[A/C]AATAACTAGAAAAGT	10342
rs144969743	snp	A/G	0.00358779	0.0422022	intron-variant	TFG	GRCh38.p7	3:100729021	TTCCTAAACTTTGCT[A/G]TTCATCAGAATTACT	10342
rs145057582	in-del	-/T	0.00755907	0.0610114	utr-variant-3-prime	TFG	GRCh38.p7	3:100748640	TTTAAAAGCAGAGCA[-/T]TTTTTTATGATATCA	10342
rs145068939	snp	A/C	0.00517822	0.0506191	intron-variant	TFG	GRCh38.p7	3:100734564	TTTTATTGGGGTAAA[A/C]TCCTCTGGTTTCTGA	10342
rs145104559	snp	A/G	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100737220	GAAAAAAAGCAGTGT[A/G]TTTTAAGTCAGACTT	10342
rs145209312	in-del	-/AGAT	0.00716266	0.059414	downstream-variant-500B, utr-variant-3-prime	TFG, ABI3BP	GRCh38.p7	3:100749405	TAGCGTTGATAAGAT[-/AGAT]TGAAGCATGTTGAAA	10342
rs145391261	snp	C/T	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100711234	CAGTCTCCTGAGTAT[C/T]TGGGATTACAGGCGT	10342
rs145466793	snp	C/G			intron-variant	TFG	GRCh38.p7	3:100716244	TGCAGCCTCTACTGT[C/G]ATCTGTTCTGCTTTT	10342
rs145495077	snp	C/T	0.00993419	0.0697739	upstream-variant-2KB	TFG	GRCh38.p7	3:100708277	TAACCAATCCAGCTG[C/T]TTCTGTACTTCACTG	10342
rs145559125	in-del	-/AC	0.0659589	0.169201	intron-variant	TFG	GRCh38.p7	3:100746619	GGAGACTATATATAT[-/AC]ACACACACACATGAT	10342
rs145570102	snp	C/T	0.00517822	0.0506191	intron-variant	TFG	GRCh38.p7	3:100725340	GATACTTGGGATAAA[C/T]CTAACATGGCAAGAT	10342
rs145580726	snp	C/T	0.00119737	0.0244387	intron-variant	TFG	GRCh38.p7	3:100721806	ACTTCAGTTAAGATA[C/T]GTGATAGTCTACAAA	10342
rs145712619	snp	A/T			intron-variant	TFG	GRCh38.p7	3:100721129	TTACAGTATTGAATG[A/T]AAAATACTTAACTAT	10342
rs145735377	snp	A/G	4.94703e-05	0.0049732	synonymous-codon	TFG	GRCh38.p7	3:100728767	ATATCTCCGTCGAGA[A/G]CTGATAGAACTTCGA	10342
rs145835282	snp	A/G	0.00135322	0.0259765	missense	TFG	GRCh38.p7	3:100748316	CCTGCACAAACTTAC[A/G]CTGCCCAAACTTCTC	10342
rs145846729	snp	C/T	0.00159617	0.0282053	upstream-variant-2KB	TFG	GRCh38.p7	3:100708885	GAGAAGGGAAGAGTA[C/T]GTAGGACACACTCAA	10342
rs145889213	snp	A/G	0.00517822	0.0506191	intron-variant	TFG	GRCh38.p7	3:100733724	GTTGTAGTGACTTGG[A/G]CTTATATTCTTTTGA	10342
rs145939508	snp	A/C	0.00517822	0.0506191	intron-variant, upstream-variant-2KB	TFG	GRCh38.p7	3:100710737	TATACAAGTTAGAAG[A/C]CGAGTCATTTCTGGA	10342
rs145957989	snp	A/G	0.00318978	0.0398085	intron-variant	TFG	GRCh38.p7	3:100713449	AGAAAAAATAATAGT[A/G]GACGTAAAATAAAAG	10342
rs146004809	snp	C/T	1.64996e-05	0.0028722	missense, intron-variant	TFG	GRCh38.p7	3:100736711	CTCAAGCAGGTCAGA[C/T]TGAAGGTAAAATAGA	10342
rs146047683	in-del	-/A			intron-variant	TFG	GRCh38.p7	3:100724374	TATAGTAGAAACTTT[-/A]AAAATTTATATATAC	10342
rs146060181	snp	C/T	0.0217236	0.101931	intron-variant	TFG	GRCh38.p7	3:100728348	TAAATTTAATAATTT[C/T]TATTAAATTTAATAA	10342
rs146078119	snp	C/T	0.000399281	0.0141238	missense	TFG	GRCh38.p7	3:100748475	CCTAATCCTTATGCG[C/T]GTAACCGTCCTCCCT	10342
rs146081098	snp	A/G	0.0023933	0.0345097	intron-variant	TFG	GRCh38.p7	3:100731083	GCCAGTGTGTGCTGT[A/G]GGTACTTATATTCGG	10342
rs146183551	snp	A/T	0.00517822	0.0506191	intron-variant	TFG	GRCh38.p7	3:100745036	ATTGATATAATAGGT[A/T]TTAAGTTTTTATTAG	10342
rs146202800	snp	A/G	9.9272e-05	0.00704458	missense	TFG	GRCh38.p7	3:100748476	CTAATCCTTATGCGC[A/G]TAACCGTCCTCCCTT	10342
rs146354348	snp	C/T	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100742354	GATCACAAAAATACC[C/T]CCAGACTTCTAGATA	10342
rs146375360	in-del	-/T			intron-variant	TFG	GRCh38.p7	3:100742732	GGAATAATTTTTTTT[-/T]CCTTCTCAGTGTTTT	10342
rs146510520	snp	A/G	0.0023933	0.0345097	intron-variant	TFG	GRCh38.p7	3:100721926	GAGGCCAAGGCGGGC[A/G]GATTGCCTGAGTGCA	10342
rs146647314	snp	G/T	0.00676609	0.0577691	intron-variant	TFG	GRCh38.p7	3:100739442	TCATATAAAGCCAGT[G/T]CCTGTTACAGGAAGA	10342
rs146808807	in-del	-/TTAG	0.00318978	0.0398085	intron-variant	TFG	GRCh38.p7	3:100724310	AAATCTTTATGAGGA[-/TTAG]TTAAGGAGAAACAAG	10342
rs146870214	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100745275	CCTCTCCATTTATAT[A/G]TAACACGTAATTCCA	10342
rs146889339	snp	A/C	0.00517822	0.0506191	upstream-variant-2KB	TFG	GRCh38.p7	3:100708439	CCTTTAAATTTAATT[A/C]AGCTTAAGTTTTTCT	10342
rs147033614	snp	C/T	0.0166325	0.0896639	intron-variant, upstream-variant-2KB, utr-variant-5-prime	TFG	GRCh38.p7	3:100710127	AATACCCGAAGGAGC[C/T]CGGAAGGGTGTGGAG	10342
rs147227120	snp	C/T	0.0023933	0.0345097	intron-variant	TFG	GRCh38.p7	3:100738177	TGAATCAGTGGTTTG[C/T]GAAGAATTTCTTATT	10342
rs147299025	snp	A/G	0.00199481	0.0315187	intron-variant	TFG	GRCh38.p7	3:100724553	AACAGATGATTCTAA[A/G]TTATACAAACTATTC	10342
rs147315783	snp	A/G	0.00159617	0.0282053	intron-variant	TFG	GRCh38.p7	3:100727114	CTATCACAGATTATA[A/G]TCTTGTGTGATGTTG	10342
rs147368104	in-del	-/TGTAG	0.0573587	0.15934	intron-variant	TFG	GRCh38.p7	3:100745013	CTTAATTCCTTGATT[-/TGTAG]TACATTGATATAATA	10342
rs147404890	snp	C/T	0.0107246	0.0724382	intron-variant	TFG	GRCh38.p7	3:100739006	ATTTCAAACAAGCCA[C/T]ATTTCAGGTGCTCAA	10342
rs147421587	snp	C/T	0.0023933	0.0345097	intron-variant	TFG	GRCh38.p7	3:100743382	TTTTTATTTTAGATT[C/T]TGGTCACTTCTATTC	10342
rs147546544	snp	A/T	8.27109e-05	0.00643029	synonymous-codon	TFG	GRCh38.p7	3:100720024	CCTTTCCTTTGCAAT[A/T]CAGTGCAGTAGGATA	10342
rs147643235	in-del	-/TTTT			intron-variant	TFG	GRCh38.p7	3:100718550	TTTTTTTTTTTTTTT[-/TTTT]GAGACAAAGTCTTGC	10342
rs147686421	snp	G/T	0.00993419	0.0697739	intron-variant	TFG	GRCh38.p7	3:100716278	TTGTATAAGATCAAC[G/T]TTTTTTAGCTTCCAC	10342
rs147702539	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100720463	GCCAACCTTTTTGCA[C/T]TGGAAACTGGTTTCG	10342
rs147790951	snp	C/T	0.00318978	0.0398085	intron-variant	TFG	GRCh38.p7	3:100733044	ATTTGATTTGTCTTA[C/T]CTCCTCATCTTAGAG	10342
rs147807984	snp	C/T	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100735574	TAGTGAGTGACAGCA[C/T]TAGGATTTGAACCTG	10342
rs147930713	snp	A/T	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100716016	ATATAATGGGATTAG[A/T]TCAGGGTAATTCGCA	10342
rs148039733	snp	A/G	0.00318978	0.0398085	intron-variant	TFG	GRCh38.p7	3:100743833	ACTTCAGCAGTAAGT[A/G]TCTGGTTTGCTCATA	10342
rs148091587	snp	C/T	0.00279162	0.0372561	intron-variant	TFG	GRCh38.p7	3:100737805	TATAATCCCAGCACT[C/T]TGGGAGGCCGAGCCA	10342
rs148250975	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	TFG	GRCh38.p7	3:100710436	AGTGAGAATCTTTAC[C/T]GTCTTGCTGCACTGC	10342
rs148372078	snp	A/T	0.00119737	0.0244387	intron-variant	TFG	GRCh38.p7	3:100730061	CAAACAAAAATTTCC[A/T]ATTTTAGATCAAGAA	10342
rs148408757	snp	A/C	0.000798403	0.0199641	upstream-variant-2KB	TFG	GRCh38.p7	3:100708375	TCTTAATCTGCTGTG[A/C]TTCTGGGGGCTGCCC	10342
rs148479730	snp	C/T	0.0134861	0.0810011	intron-variant	TFG	GRCh38.p7	3:100732155	GTGCCCAGTGGGTAT[C/T]TGATACTAGGATATA	10342
rs148531260	snp	G/T	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100728170	TTTCTTTTAAGATCA[G/T]CTATTTTAGTTAGCT	10342
rs148618705	snp	C/T	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100739294	AGTTGTTACTTAACT[C/T]CCATAAAAGGGACTT	10342
rs148758742	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100724692	TAGATAGAAAATATT[A/G]AGTAATATTTACAAA	10342
rs148829000	in-del	-/T	0.303438	0.244222	intron-variant	TFG	GRCh38.p7	3:100717580	TTTCTTTCATCAGTG[-/T]TTTTTTTTTTTTTTG	10342
rs148835012	snp	A/G	0.000132833	0.00814855	synonymous-codon	TFG	GRCh38.p7	3:100748177	GCAGACTGGACCTCA[A/G]CAACCTCAGCAGTTC	10342
rs148867194	snp	A/C	0.00517822	0.0506191	intron-variant	TFG	GRCh38.p7	3:100725485	GCAAAGATGAAAAAA[A/C]TACTAAGATTTGGCC	10342
rs148918849	snp	C/T	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100721665	AAAGGCCAAAATCTC[C/T]CTTGAGGGGTATATT	10342
rs148988779	snp	A/G	0.00119737	0.0244387	intron-variant	TFG	GRCh38.p7	3:100745367	TTAAATAAGAGCTCA[A/G]TTAAGCTACTTAGAT	10342
rs149039595	in-del	-/TG	0.0573587	0.15934	intron-variant	TFG	GRCh38.p7	3:100718276	GCCTTTATCTCAAAC[-/TG]ACCTCATTGACTGGC	10342
rs149089836	in-del	-/AAA	0.0134861	0.0810011	intron-variant	TFG	GRCh38.p7	3:100736856	ACATGATTTGATGTT[-/AAA]AAACCAAATAGAACA	10342
rs149148159	snp	G/T	0.00953873	0.0683987	intron-variant	TFG	GRCh38.p7	3:100742155	CTTAATTAATTTTCA[G/T]AATACTGTGACAGTC	10342
rs149198442	snp	A/G	0.00517822	0.0506191	intron-variant	TFG	GRCh38.p7	3:100711257	ACAGGCGTGCGCCAC[A/G]ACAACTGGCTCATTT	10342
rs149306856	snp	A/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100712280	TGAAAACTTTTTTGA[A/T]GTACTTGAAGGGTTG	10342
rs149396913	snp	G/T	0.00438332	0.0466095	intron-variant	TFG	GRCh38.p7	3:100727461	TATTTTCACGTAGAT[G/T]TCCTTTTCTAATTAG	10342
rs149450472	snp	C/T	0.0217236	0.101931	intron-variant	TFG	GRCh38.p7	3:100723604	AACAGAATAGACTTA[C/T]ATAAAAACTTGAGTA	10342
rs149539646	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100735265	GACTGTCAGCTGTCA[A/G]CTGTGCCTAATACTG	10342
rs149695544	snp	A/C	0.00517822	0.0506191	upstream-variant-2KB	TFG	GRCh38.p7	3:100708192	ATAAGCGAGTCTTGG[A/C]CAATTCCAGCCGCCA	10342
rs149785062	snp	C/G	0.0023933	0.0345097	intron-variant	TFG	GRCh38.p7	3:100720700	GGTTGGGGACCCTTG[C/G]TTTAGACAGTATTTC	10342
rs149837398	snp	A/G	0.00478085	0.0486577	intron-variant	TFG	GRCh38.p7	3:100715674	TTATGCTTATCATAC[A/G]TTGATTTGCACCTCT	10342
rs149908287	snp	A/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100739119	ATAGGCTACTTTTAC[A/T]TTTTGTTGTATAATG	10342
rs149927288	snp	C/G/T	0.00068256	0.0184614	intron-variant	TFG	GRCh38.p7	3:100728865	CTGAAAATGGTAAAC[C/G/T]CTGAATCCATTGTAT	10342
rs149970772	in-del	-/TC	0.00517822	0.0506191	intron-variant	TFG	GRCh38.p7	3:100743596	GATTTTTATTTGTAT[-/TC]TTTTTTTATTATAAA	10342
rs150224373	snp	A/G	0.0023933	0.0345097	intron-variant, upstream-variant-2KB, utr-variant-5-prime	TFG	GRCh38.p7	3:100709521	CCTGCCACGTACAGA[A/G]CCCAAGTTCTCGCTA	10342
rs150294144	snp	C/T	0.00557542	0.0525036	intron-variant	TFG	GRCh38.p7	3:100733619	CCTCTCCCCCACACA[C/T]ACTCCCCCCAACTCC	10342
rs150308181	in-del	-/AAAT	0.00835141	0.0640778	downstream-variant-500B	TFG, ABI3BP	GRCh38.p7	3:100749311	TGATGAACCATTCAG[-/AAAT]AAATAACAAACAAAA	10342
rs150364470	snp	C/T	0.00358779	0.0422022	intron-variant	TFG	GRCh38.p7	3:100716739	CCATCCTAACTGGGG[C/T]GAACCTTGTTGTGGT	10342
rs150435581	snp	C/T	0.0111196	0.0737302	intron-variant	TFG	GRCh38.p7	3:100741426	TTAAAATTAAAAGAA[C/T]AGAAAAATGCTTATA	10342
rs150488725	snp	A/G	1.64868e-05	0.00287109	synonymous-codon	TFG	GRCh38.p7	3:100736676	TCAGCCACAGCAGCC[A/G]CCATATACAGGAGCT	10342
rs150545034	snp	C/G			intron-variant	TFG	GRCh38.p7	3:100744334	TCCAAAAGTGTCTTT[C/G]AGCTCTGGAACAAAA	10342
rs150561256	snp	A/T	0.00159617	0.0282053	upstream-variant-2KB	TFG	GRCh38.p7	3:100707923	TAAACTTACATTATT[A/T]CACTCTCAAACAGAA	10342
rs150620449	snp	G/T	0.00223264	0.0333367	synonymous-codon	TFG	GRCh38.p7	3:100720048	TAGGATACTGAAACT[G/T]ACATTATTTGGTGAG	10342
rs150701125	snp	C/G	0.0256215	0.110247	intron-variant	TFG	GRCh38.p7	3:100714423	GAGAATTACTTGAAC[C/G]CGGGAGGTGGAGCTT	10342
rs150842663	snp	C/T	0.00159617	0.0282053	intron-variant	TFG	GRCh38.p7	3:100725028	CCCATCTCAGCTTCC[C/T]GAGTAGCTGGGACTA	10342
rs150876309	snp	A/C	0.00993419	0.0697739	intron-variant	TFG	GRCh38.p7	3:100730285	TTTTTGCTTTAGGTG[A/C]AACTTTTTCCTCACC	10342
rs150933046	snp	G/T	0.0166325	0.0896639	intron-variant	TFG	GRCh38.p7	3:100736154	AGGCATGTGAGAAGA[G/T]AAATTGTGAGAAATA	10342
rs151074626	snp	C/T	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100745998	GTCATTAATTAAAAT[C/T]TGAAATATTTTGACA	10342
rs151284869	snp	C/T	0.00953873	0.0683987	intron-variant	TFG	GRCh38.p7	3:100711347	ACCTCGTGATCTGCC[C/T]GCCTCGGCCTCCCAA	10342
rs180769412	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100725005	GCCTCCGGGGCTCAC[C/T]CCATTCTCCCATCTC	10342
rs180996914	snp	A/C	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100712892	GAAAGGGTCAAGACA[A/C]AGGGAAAACTTGAAG	10342
rs181112569	snp	C/T	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100724239	AATAATAAGAGCAGA[C/T]GTGAACTAGAAATTG	10342
rs181319138	snp	A/C	0.00716266	0.059414	upstream-variant-2KB	TFG	GRCh38.p7	3:100708690	TCATCCTCCACCACC[A/C]CCAGGTGATGTCTGC	10342
rs181330183	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100729268	TCATGAATAATTACA[C/T]AGTGTTGGAAGTATT	10342
rs181455025	snp	C/T	0.00159617	0.0282053	intron-variant	TFG	GRCh38.p7	3:100720571	CAATAGGGTTCACAC[C/T]CCTATGTGAATCTAA	10342
rs181525104	snp	C/T	0.00755907	0.0610114	intron-variant	TFG	GRCh38.p7	3:100743398	TGGTCACTTCTATTC[C/T]GAAAGTTAGTTATGA	10342
rs181598398	snp	G/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100744366	ATGTCATATAGTTCC[G/T]TGCTACCAAAGAGTT	10342
rs181736342	snp	A/C	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100720161	AGCAATAACTTATTC[A/C]AATATTATTACATTT	10342
rs181777182	snp	A/G	0.00755907	0.0610114	intron-variant	TFG	GRCh38.p7	3:100719082	TGTTATGGGAAGTGG[A/G]TCTGGCTATAAGGAG	10342
rs181797193	snp	A/G	0.00119737	0.0244387	intron-variant	TFG	GRCh38.p7	3:100742051	CTATAAACAATGTCT[A/G]CATTTTGCTCTCTTC	10342
rs181800796	snp	A/T	0.031825	0.122064	intron-variant	TFG	GRCh38.p7	3:100728571	GAGAATTCTTTTTTT[A/T]TAAAAAAAAAGTTAC	10342
rs181937717	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	TFG	GRCh38.p7	3:100708905	GACACACTCAAATGC[C/T]TTATCCTCTAAAAAT	10342
rs182061215	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100713417	AAATGGTCATGTCAG[A/G]TGAACAGTTAAATAT	10342
rs182077211	snp	G/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100737750	ATCATCCTGTGGTGA[G/T]ACTTTCAGAGTTACC	10342
rs182228082	snp	A/G	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100731046	AGCCTGGAATGGTAT[A/G]TTAGGAATGAATGAG	10342
rs182505840	snp	A/G	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100738890	CCTAATGTATCCAAC[A/G]TGTACTCACTATTAA	10342
rs182542007	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100738452	GTTTGCTGTTTATGT[A/G]TAAATAAATGGGAAT	10342
rs182554215	snp	G/T	0.000399281	0.0141238	downstream-variant-500B, utr-variant-3-prime	TFG, ABI3BP	GRCh38.p7	3:100749378	AGAATTTATACTTGT[G/T]TGAAAAATACAAAAT	10342
rs182556158	snp	C/T	0.00159617	0.0282053	intron-variant	TFG	GRCh38.p7	3:100726009	TTACAAGGCGAAGTC[C/T]GGTGATAGGCCATCT	10342
rs182688059	snp	C/T	0.00478085	0.0486577	intron-variant	TFG	GRCh38.p7	3:100734347	GATATCCTCGTCTGC[C/T]CTCCCAGCCCTATAG	10342
rs182764806	snp	A/C	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100714815	AAGTTAGTAGTATGC[A/C]GTGTTCCCAGACTCA	10342
rs182959769	snp	A/G	0.00119737	0.0244387	intron-variant	TFG	GRCh38.p7	3:100733022	TTAGTTGCAGTATTC[A/G]AATTATATTTGATTT	10342
rs183107149	snp	C/T	0.00199481	0.0315187	intron-variant	TFG	GRCh38.p7	3:100721399	CATCTGGTGTCTACA[C/T]GGTGTAGGCCCTTGG	10342
rs183118682	snp	A/G	0.00159617	0.0282053	intron-variant	TFG	GRCh38.p7	3:100746003	TAATTAAAATTTGAA[A/G]TATTTTGACACAATT	10342
rs183239613	snp	C/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100715650	GGATAGTACTTTTTT[C/G]CTGTTTTCTTATGCT	10342
rs183267036	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100739385	TCAACAAGATATTGA[A/G]CATCATTAAAAAAAA	10342
rs183368255	snp	A/G	0.00159617	0.0282053	intron-variant	TFG	GRCh38.p7	3:100746315	ATTTCATTTGATTGG[A/G]TGTGGGACTCAGGCG	10342
rs183606004	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100722022	CAGCTGTAGTGGTGT[A/G]TGCCTGTAGTCCCAG	10342
rs183734166	snp	C/T	0.00159617	0.0282053	intron-variant, utr-variant-5-prime	TFG	GRCh38.p7	3:100710988	GACTGCAAGAGCAAA[C/T]GACAGCTTTAGGAAA	10342
rs183743841	snp	C/T	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100727579	CAGAGCCTTGTGTCA[C/T]TTTCTTTTTAAAAAT	10342
rs183885488	snp	A/G	0.000954704	0.0218275	utr-variant-3-prime	TFG	GRCh38.p7	3:100748556	TCTACACCAATTAAT[A/G]TAGCTGCTAGCTATT	10342
rs183892295	snp	A/G	0.00199481	0.0315187	intron-variant	TFG	GRCh38.p7	3:100723582	AATGCAAAGAAAGCT[A/G]GTTATTAACAGAATA	10342
rs183934201	snp	A/G	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100735483	CCTTATCAAGTAGGA[A/G]TTAGTATATCCTTTG	10342
rs184097099	snp	A/T			intron-variant	TFG	GRCh38.p7	3:100725785	GTGACAGAGCAAGAC[A/T]CTGTCTCAAAAAAAA	10342
rs184298243	snp	A/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100711484	TATCTTCAAAGCTGG[A/T]ATTTTTTTCTTAATT	10342
rs184305199	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100735830	ACAAAAAGAATCAAC[A/G]GTCAGGAGCCCGGCC	10342
rs184336057	snp	A/G	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100741128	ATTTGTGAATTTACT[A/G]TACTATATTTTTAAA	10342
rs184425200	snp	C/T	0.0111196	0.0737302	intron-variant	TFG	GRCh38.p7	3:100728602	TCCATTACATTGATA[C/T]CTTGTTTTTGTTTTT	10342
rs184430770	snp	A/G	0	0	upstream-variant-2KB	TFG	GRCh38.p7	3:100708488	CTGGAGACCAGGTAG[A/G]GTCTAAATGCTTTAT	10342
rs184443193	snp	A/G	0.00199481	0.0315187	intron-variant	TFG	GRCh38.p7	3:100717743	TATTTTGTTTCTGGC[A/G]GCTTTATTGAATTCA	10342
rs184644353	snp	G/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100716676	GTGTAAGAGTTCCCT[G/T]TTCTCTTCATTCTTG	10342
rs184781223	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100740253	TTAGACAGATATCCC[A/G]GAATGGTTTAGCTGG	10342
rs184784052	snp	A/G	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100722766	GAAAAGTAGCATCCT[A/G]TACTCCACTAAATTT	10342
rs184813827	snp	A/C	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100736467	CGTATTTGTGGTTAT[A/C]TACTTATTCTATAGT	10342
rs184882356	snp	A/G	0.0119091	0.0762411	intron-variant	TFG	GRCh38.p7	3:100720897	AAATAAAATGTGTAC[A/G]CTTTTTCCGGCTGTT	10342
rs184910095	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100712023	GTATTCTTATTTTGC[A/G]TTAAGATAAGCATGG	10342
rs184918989	snp	G/T	0.00557542	0.0525036	intron-variant	TFG	GRCh38.p7	3:100747206	CATTGGACCATCTTT[G/T]ACACTGTTGGTTTGC	10342
rs184965074	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100742653	GAAATTGAAGTGCCC[A/G]GAGAAAACCCACACA	10342
rs185078148	snp	A/C	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100730036	TTGCCTATTCTGAGC[A/C]CTACCTCTCCAAACA	10342
rs185165011	snp	A/G	0.000798403	0.0199641	downstream-variant-500B, utr-variant-3-prime	TFG, ABI3BP	GRCh38.p7	3:100749403	CAAAATGTAGCGTTG[A/G]TAAGATTGAAGCATG	10342
rs185214240	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100725197	AGATATGAGCCACCA[C/T]GCCTGGCCAAAAGGG	10342
rs185270664	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100724225	ATAACTTGGAAGGAA[A/G]TAATAAGAGCAGACG	10342
rs185528345	snp	A/G	0.00398564	0.0444627	intron-variant	TFG	GRCh38.p7	3:100724590	ATAGGCAAAGAGGGA[A/G]TATACACTAATTCAT	10342
rs185581189	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100728152	CATATATTTTTTTAA[C/T]GATTTCTTTTAAGAT	10342
rs185701987	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	TFG	GRCh38.p7	3:100708252	TTCAAATAAGGCCAA[C/T]GCCAACCTGTAACCA	10342
rs185779153	snp	A/G	0.00716266	0.059414	intron-variant	TFG	GRCh38.p7	3:100745267	TCCCTCCACCTCTCC[A/G]TTTATATGTAACACG	10342
rs185908616	snp	A/T	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100737928	GCCAGGTGCTATGGC[A/T]TGTGCCTATAGTTCC	10342
rs185934660	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	TFG	GRCh38.p7	3:100708812	CACTGACCGACTTCC[A/G]CCCCTTGGCTATAAA	10342
rs186077668	snp	A/G	0.00478085	0.0486577	intron-variant	TFG	GRCh38.p7	3:100713063	TAGGTTTTACTTAAC[A/G]GTGTTAACTCTGGTG	10342
rs186086461	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100713453	AAAATAATAGTAGAC[A/G]TAAAATAAAAGCTTA	10342
rs186235725	snp	C/T	0.00755907	0.0610114	intron-variant, upstream-variant-2KB, utr-variant-5-prime	TFG	GRCh38.p7	3:100710175	AGTTGATTGGGGTCA[C/T]AGAATCGGAGCCTAG	10342
rs186247817	snp	A/C	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100733627	CCACACACACTCCCC[A/C]CAACTCCAGTAGGGT	10342
rs186447013	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100738548	AAATTTTAAAAATGC[A/G]AAAGGACATACAGTG	10342
rs186466460	snp	G/T	0.0107246	0.0724382	intron-variant	TFG	GRCh38.p7	3:100719083	GTTATGGGAAGTGGG[G/T]CTGGCTATAAGGAGC	10342
rs186634162	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100723082	ATGTGTACGTTTTAA[C/T]GAGCATTGATTGTTA	10342
rs186650823	snp	A/G	0.00358779	0.0422022	intron-variant	TFG	GRCh38.p7	3:100714260	ATCCCAGCACTTTGG[A/G]AGACCGAGGTAGGCG	10342
rs186659523	snp	A/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100747538	AGTAAATAATGAATA[A/T]AGATGTTGCTTTTTA	10342
rs186794564	snp	A/G	0.00597247	0.0543191	intron-variant	TFG	GRCh38.p7	3:100715379	CTGATGGTGTTGTAT[A/G]TCATTTCTGCCCTTA	10342
rs186915793	snp	A/C	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100720429	TAACATGTAAGTCTG[A/C]TACTTGAAACCAGTA	10342
rs187102705	snp	A/G	0.0107246	0.0724382	intron-variant	TFG	GRCh38.p7	3:100744141	GGTTTCTTCATAGGA[A/G]CAGTGGTTGTTGACC	10342
rs187223006	snp	C/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100716092	ATATTCTCCTTCTAG[C/G]TATTTGAAATTATAT	10342
rs187245034	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100739491	AATGTAACTGGTAAG[A/G]AGAAGAACGCTAAAA	10342
rs187254626	snp	C/T	0.0107246	0.0724382	intron-variant	TFG	GRCh38.p7	3:100726820	ATTTTGGATAAGGTT[C/T]AAGGAAGTAGAGCTT	10342
rs187270210	snp	C/T	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100731254	TTTTGTTTACTTGTT[C/T]GTGTTTTTTGTTTGT	10342
rs187442311	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TFG	GRCh38.p7	3:100710539	GAAGGAAACTGCTCC[C/T]CTCAGGAGGTGCTTA	10342
rs187498385	snp	A/G	0.00279162	0.0372561	upstream-variant-2KB	TFG	GRCh38.p7	3:100709275	ATACCCGCTTTCGAG[A/G]AAACCGGAAGTGCGT	10342
rs187702670	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100734912	ATGCATAGCTAGGAT[A/G]CTTTTGTAGTTCTTC	10342
rs187769812	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100727646	GATTTCATTTTTTTC[A/G]GTCAACTGAAAATCA	10342
rs187832694	snp	C/G	0.00279162	0.0372561	intron-variant	TFG	GRCh38.p7	3:100721829	TCTACAAAATTAAAA[C/G]TTATTTAAGACATAG	10342
rs188032258	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	TFG	GRCh38.p7	3:100707613	TTTAAATATACTACT[A/G]TAACAGTAGTATAAT	10342
rs188038211	snp	A/C	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100739241	CATAGCAATCTCTTA[A/C]AATGTGTTAATAGTC	10342
rs188296676	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100741304	CCAGTGGGACAGGAT[A/G]TGGAGGTGGAAAATA	10342
rs188472126	snp	C/T	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100718668	GTTCAAGTGATTCTC[C/T]TGCCTCGGCCTCCCA	10342
rs188479249	snp	G/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100725904	TTATATTCACACTAA[G/T]GAAGATACATTATTA	10342
rs188480123	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	TFG	GRCh38.p7	3:100708501	AGGGTCTAAATGCTT[C/T]ATTTATCAGCTTAGT	10342
rs188492296	snp	C/T	0.000402637	0.014183	intron-variant	TFG	GRCh38.p7	3:100728890	TTGTATTCTGACTTA[C/T]TGTTCTTACGTCTTT	10342
rs188548566	snp	C/T	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100722107	AGTGAGTCGAGATCG[C/T]GCCACTGCACTCCAG	10342
rs188679289	snp	A/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100735530	GAGGCACAGAAAGAG[A/T]TTATGTAACATGTCC	10342
rs188841493	snp	C/T	0.00159617	0.0282053	intron-variant	TFG	GRCh38.p7	3:100746618	GGGAGACTATATATA[C/T]ACACACACACACATG	10342
rs188938237	snp	A/T	0.00119737	0.0244387	intron-variant	TFG	GRCh38.p7	3:100719780	TTGCCATAAGAGTAA[A/T]AAGCAAAATTGATTT	10342
rs188948596	snp	C/T	0.00279162	0.0372561	intron-variant	TFG	GRCh38.p7	3:100743249	TAAATGTGTTTATTG[C/T]CTGTTTGCTTATTTT	10342
rs189027146	snp	G/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100712082	TGTTCTGCATTGACC[G/T]TAGAGTGTTATATTT	10342
rs189113409	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100711565	GTGAGGGGTCGGATG[C/T]AAAAACTGATCTATA	10342
rs189131409	snp	A/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100735858	GCCAAAAGAGTGCAG[A/T]GTCTTTAAGAGGGAA	10342
rs189196153	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100731036	ATATTAGGGTAGCCT[A/G]GAATGGTATGTTAGG	10342
rs189319922	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100736504	AGTATCTTTTAACCA[A/G]ACTTATTCCTTGAGC	10342
rs189396633	snp	G/T	0.0023933	0.0345097	downstream-variant-500B	TFG, ABI3BP	GRCh38.p7	3:100749089	ACTAACTTACAGATT[G/T]CCATTCAGAGAAAAC	10342
rs189400604	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100723623	AAAACTTGAGTAGTA[A/G]TAGTCACTTTATGAT	10342
rs189412388	snp	A/G	0.00199481	0.0315187	intron-variant	TFG	GRCh38.p7	3:100713108	TAAAAGTGGGCAAAG[A/G]TAAAAAGCAGGCAGA	10342
rs189489590	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100740706	GGGTCATGATAGAGG[C/T]TGGCTACTCTGTGTA	10342
rs189597535	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100724715	TTTACAAATCAAACT[C/T]ATCAGTGAATATTTA	10342
rs189737698	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100720999	ATATGATCATGGTCT[A/G]TTGATTTAATTTGTA	10342
rs189760519	snp	C/G	0.00318978	0.0398085	intron-variant	TFG	GRCh38.p7	3:100745854	TATTCTCTACTGCTA[C/G]TTGGGCACTAGAATG	10342
rs189771059	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100717231	CTATGTGTTTGTTCT[C/T]TTGGTCAATGGGTCT	10342
rs189851471	snp	A/C/T	0.000399281	0.0141238	upstream-variant-2KB	TFG	GRCh38.p7	3:100708339	TCTATAAATCTTCCA[A/C/T]CACGTGGCTCTGCTG	10342
rs189990998	snp	A/T	0.00119737	0.0244387	intron-variant	TFG	GRCh38.p7	3:100724228	ACTTGGAAGGAAATA[A/T]TAAGAGCAGACGTGA	10342
rs190093317	snp	G/T			intron-variant	TFG	GRCh38.p7	3:100728260	CTTTAAACATGTATA[G/T]AGTAAGGTATTTTTG	10342
rs190211383	snp	G/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB, utr-variant-5-prime	TFG	GRCh38.p7	3:100710185	GGTCATAGAATCGGA[G/T]CCTAGTTCCTTGGCT	10342
rs190231832	snp	A/G	0.00199481	0.0315187	intron-variant	TFG	GRCh38.p7	3:100733740	CTTATATTCTTTTGA[A/G]GATTTTCTGTTATTG	10342
rs190343745	snp	C/T	0.00119737	0.0244387	intron-variant	TFG	GRCh38.p7	3:100737669	AGTGATTAAGGTTAT[C/T]AATTACATTAAAACA	10342
rs190536612	snp	A/G	0.00557542	0.0525036	utr-variant-5-prime, upstream-variant-2KB	TFG	GRCh38.p7	3:100709361	ATCCAGTGAGAAAGC[A/G]GGGACTCTTCGGCCT	10342
rs190654500	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100713549	GGGATAATGAATCTT[C/T]TGGAGGCTAGAGTTT	10342
rs190673048	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100738267	CCAAAACTAGAACAA[A/G]CTAGAACTAAAGCAG	10342
rs191003968	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100746233	AATCTCGGGATTTCG[A/G]TCCTCACTATGCTTT	10342
rs191029429	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	TFG	GRCh38.p7	3:100708864	TTTCTATTTGAACAG[A/G]TAAGGGAGAAGGGAA	10342
rs191152647	snp	C/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100744365	GATGTCATATAGTTC[C/G]TTGCTACCAAAGAGT	10342
rs191295634	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100714454	ACATTGAGCCAAGAT[C/T]GTGCCACTGCACTCC	10342
rs191380185	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100720522	CAGGAGAAGGTTTGG[A/G]GATGAAACTCTTCCA	10342
rs191484683	snp	A/G	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100711748	TTGTAGGAAGGAGAA[A/G]GTAACAAATACATTG	10342
rs191493868	snp	A/T	0.00159617	0.0282053	intron-variant	TFG	GRCh38.p7	3:100723475	CTCTTAATGGAATTT[A/T]AAAAAAAATCCAGTT	10342
rs191500949	snp	C/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100735859	CCAAAAGAGTGCAGA[C/G]TCTTTAAGAGGGAAA	10342
rs191501984	snp	A/G	1.66446e-05	0.00288479	missense	TFG	GRCh38.p7	3:100748494	ACCGTCCTCCCTTTG[A/G]TCAGGGCTATACCCA	10342
rs191527708	snp	A/C	0.00159617	0.0282053	intron-variant	TFG	GRCh38.p7	3:100738763	CTATTAATAACTGAT[A/C]TAATTCTAGATCAGT	10342
rs191619136	snp	A/C	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100725928	ATTATTATGTGTGCT[A/C]GGGTTCTCCAGAGGG	10342
rs191727673	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100732020	GTTGGCTTGATTTCC[A/G]TGTAATTTAATAGTG	10342
rs191888866	snp	A/T	0.00119737	0.0244387	intron-variant	TFG	GRCh38.p7	3:100727150	CTTTGAAATATTTAT[A/T]TTCAACGGGAGAACA	10342
rs192059503	snp	A/T	0.00636936	0.0560724	intron-variant	TFG	GRCh38.p7	3:100721993	CTATCTCTACTGAAA[A/T]GCAAAAAATTAGCCA	10342
rs192147065	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100716106	GCTATTTGAAATTAT[A/G]TAATATGTTATTGTT	10342
rs192162544	snp	A/C	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100739618	AGCTGAGTAGCCTTT[A/C]TTATGTAAATATTGA	10342
rs192264496	snp	C/T	0.00159617	0.0282053	intron-variant	TFG	GRCh38.p7	3:100725506	AGATTTGGCCAGGTG[C/T]GGTGGCTCACACCTG	10342
rs192373517	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100735219	TGCATTACCACTATT[A/G]TATCCTAGTTTAGGT	10342
rs192472785	snp	A/G	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100715406	CTTATGACATTGGTC[A/G]GTACCCAGTTACATG	10342
rs192488141	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100739316	AAGGGACTTTGGAAC[C/T]GTGAATTTTATTCCA	10342
rs192531120	snp	C/T	0.0023933	0.0345097	intron-variant	TFG	GRCh38.p7	3:100746748	AGATTACTTCCAGGC[C/T]CAGTTAAAAAAAAAC	10342
rs192637703	snp	C/T	0.00478085	0.0486577	intron-variant	TFG	GRCh38.p7	3:100711394	GTGTGAGCCACCGTG[C/T]CCGGCCCTCAAATTT	10342
rs192735867	snp	C/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	TFG	GRCh38.p7	3:100710670	TATATGACCTTGGGC[C/G]TGTCAGATTATTCCC	10342
rs192776258	snp	C/T	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100717431	GGTTTGTTTTTAAAT[C/T]TTTATGAATAATTTT	10342
rs192911154	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100722733	ATCACAGTTGCAAAC[A/G]GTAAAGAAAAATAAC	10342
rs192982693	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100741051	GTCATATAAAAGTGT[A/G]GCTCACATAATTATG	10342
rs193094135	snp	A/G			upstream-variant-2KB	TFG	GRCh38.p7	3:100707952	AAGTTTCAGAGACTT[A/G]TAACTGAAAAAGATC	10342
rs193206581	snp	G/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100727838	TAAATTTATATTTAT[G/T]TTTTAAAATTTTTTG	10342
rs199724547	snp	C/T	9.9341e-05	0.00704703	missense	TFG	GRCh38.p7	3:100732637	TCAATAAAAATGTTA[C/T]GTCAGCGTTTGGCTT	10342
rs199791485	snp	A/C	1.71891e-05	0.00293159	intron-variant	TFG	GRCh38.p7	3:100732479	GATAAAAAGGAAACA[A/C]GTTTTTGTTTATTCC	10342
rs199852969	in-del	-/A	0.0225045	0.103662	intron-variant	TFG	GRCh38.p7	3:100725792	GCAAGACTCTGTCTC[-/A]AAAAAAAATATAAAT	10342
rs199973526	in-del	-/A			downstream-variant-500B	TFG, ABI3BP	GRCh38.p7	3:100749273	GTGATTTTCCTTCTC[-/A]GATAAAAGGTATAGT	10342
rs200167748	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100730170	TAACCATCTGCAGAA[C/T]ATTAAGAAGTGTAGA	10342
rs200195571	snp	A/C	6.69344e-05	0.0057847	synonymous-codon	TFG	GRCh38.p7	3:100713847	GAGTAATGATGAAGT[A/C]ACAATAAAGTATAAA	10342
rs200206121	in-del	-/AGTG			downstream-variant-500B	TFG, ABI3BP	GRCh38.p7	3:100749257	GCCTGAATAAAACTT[-/AGTG]AGTGATTTTCCTTCT	10342
rs200277448	snp	G/T			intron-variant	TFG	GRCh38.p7	3:100720281	CAGAGTGTTAAGTAT[G/T]TTTTTTTTGAAATCA	10342
rs200291758	snp	C/T			missense	TFG	GRCh38.p7	3:100728811	GTTTATTGGATAGCT[C/T]GGAACCACCTGGAGA	10342
rs200298775	in-del	-/A	0.0618563	0.164627	intron-variant	TFG	GRCh38.p7	3:100734177	ATCAGAGTTTTTAAT[-/A]TTTTTTTTAACATTA	10342
rs200304217	snp	G/T			intron-variant	TFG	GRCh38.p7	3:100720915	TTTTCCGGCTGTTTT[G/T]TTGTTTTGTTTAGCA	10342
rs200318071	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100734468	TCTTCAGCTGCTTGT[A/G]TAGCCATAAGGTTGT	10342
rs200340854	snp	A/T	0.000426412	0.0145953	intron-variant	TFG	GRCh38.p7	3:100719934	ACAAATCTGAAAATT[A/T]AAAAAATTAAAAAAC	10342
rs200661886	in-del	-/T	0.0622301	0.165053	intron-variant	TFG	GRCh38.p7	3:100728526	GACTGATAATTCTGC[-/T]TTTTTTTCCAAAATA	10342
rs200695895	snp	A/G			missense	TFG	GRCh38.p7	3:100713722	AGTGGGAAGCTAATC[A/G]TCAAAGCTCAACTTG	10342
rs200716443	snp	A/G	1.65734e-05	0.00287862	missense	TFG	GRCh38.p7	3:100713710	CAGTTGGATCTAAGT[A/G]GGAAGCTAATCATCA	10342
rs200768169	snp	C/T	1.68388e-05	0.00290158	synonymous-codon	TFG	GRCh38.p7	3:100748159	TTCAGCAAGCTATAG[C/T]CAGCAGACTGGACCT	10342
rs200924045	snp	C/T	0.00154586	0.0277586	intron-variant	TFG	GRCh38.p7	3:100713880	TGAAGGTAAGAGTGT[C/T]TTTAAAGCTATTTTT	10342
rs200957255	in-del	-/AT			intron-variant	TFG	GRCh38.p7	3:100735903	GAAATGCAAAGTAGA[-/AT]AGTCAGTATGAGTTA	10342
rs201110427	in-del	-/T	0.0150606	0.0854603	intron-variant	TFG	GRCh38.p7	3:100743041	TTGATGATGCCCAAG[-/T]TAATATTTATATTGT	10342
rs201230953	snp	G/T			downstream-variant-500B	TFG, ABI3BP	GRCh38.p7	3:100749259	CCTGAATAAAACTTA[G/T]TGATTTTCCTTCTCG	10342
rs201290760	snp	A/G	0.00609354	0.0548602	intron-variant	TFG	GRCh38.p7	3:100728874	GTAAACCCTGAATCC[A/G]TTGTATTCTGACTTA	10342
rs201326908	snp	A/G	1.68233e-05	0.00290023	synonymous-codon	TFG	GRCh38.p7	3:100713856	TGAAGTAACAATAAA[A/G]TATAAAGATGAAGGT	10342
rs201376425	in-del	-/T	0.0659589	0.169201	intron-variant	TFG	GRCh38.p7	3:100726773	TATGTTAGAAAAGTA[-/T]TTTTTTTTTGGGCTT	10342
rs201496527	snp	A/G			synonymous-codon	TFG	GRCh38.p7	3:100728776	TCGAGAACTGATAGA[A/G]CTTCGAAATAAAGTG	10342
rs201513436	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100722608	AAAATGTCTTAAGAC[A/G]GAGAGATTACCTTAA	10342
rs201620598	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100741601	AAAAATAAATGTAGT[A/G]TAGCCTAAGTGTATA	10342
rs201629915	snp	C/T			synonymous-codon	TFG	GRCh38.p7	3:100744915	GCAGCCTCAACAGTA[C/T]GGTATTCAGTATTCA	10342
rs201694302	in-del	-/TT	0.00243952	0.0348397	intron-variant, upstream-variant-2KB, utr-variant-5-prime	TFG	GRCh38.p7	3:100710267	ATGATTCTAGCTAAC[-/TT]TAAGAGTTTGCTTTG	10342
rs201727842	in-del	-/T	0.0023933	0.0345097	intron-variant	TFG	GRCh38.p7	3:100728564	AGCCATAGAGAATTC[-/T]TTTTTTTTAAAAAAA	10342
rs201734724	in-del	-/AACA			downstream-variant-500B	TFG, ABI3BP	GRCh38.p7	3:100749315	GAACCATTCAGAAAT[-/AACA]AACAAACAAAAACTC	10342
rs201899226	snp	A/C			intron-variant	TFG	GRCh38.p7	3:100728093	CCCTCCTTGGCTTCC[A/C]AAAGTGGTGGGATTA	10342
rs202007036	snp	G/T			downstream-variant-500B	TFG, ABI3BP	GRCh38.p7	3:100749263	AATAAAACTTAGTGA[G/T]TTTCCTTCTCGATAA	10342
rs202022416	in-del	-/CT	0.0383715	0.133092	utr-variant-3-prime	TFG	GRCh38.p7	3:100748752	GCAGCTTCTTAGTTA[-/CT]TTGGAACACTACTCT	10342
rs202072421	in-del	-/G/TG			intron-variant	TFG	GRCh38.p7	3:100720280	CAGAGTGTTAAGTAT[-/G/TG]GTTTTTTTTGAAATC	10342
rs202077935	in-del	-/ATCTA	0.0573587	0.15934	intron-variant	TFG	GRCh38.p7	3:100713571	CTAGAGTTTCTTAGC[-/ATCTA]ATAGTAGCTTTGCTC	10342
rs202154009	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100738621	TTTTTCAGAGGTAGC[A/G]GATTAACACTGTTTA	10342
rs207482230	snp	C/T			missense	TFG	GRCh38.p7	3:100748182	CTGGACCTCAACAAC[C/T]TCAGCAGTTCCAGGG	10342
rs367684829	in-del	-/T			intron-variant	TFG	GRCh38.p7	3:100717413	GTTCTGTACAAATTT[-/T]ATGGTTTGTTTTTAA	10342
rs367770979	snp	C/T	1.65274e-05	0.00287462	missense	TFG	GRCh38.p7	3:100748301	CAGGCGAGCAATTAT[C/T]CTGCACAAACTTACA	10342
rs367782308	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100719079	GTATGTTATGGGAAG[C/T]GGGTCTGGCTATAAG	10342
rs367852812	snp	A/G	1.65173e-05	0.00287374	intron-variant	TFG	GRCh38.p7	3:100744934	ATTCAGTATTCAGGT[A/G]AGCAGGTGTTGAAAG	10342
rs368031014	in-del	-/AAATG			intron-variant	TFG	GRCh38.p7	3:100738458	TGTTTATGTATAAAT[-/AAATG]GGAATTAAGGCGCTA	10342
rs368037715	snp	A/C			intron-variant	TFG	GRCh38.p7	3:100729612	TTCTTTTTACAAATT[A/C]TTTGTTTGCTTATAA	10342
rs368291436	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100720729	TCCCGAGGGGTACTT[A/G]AAGATTAAAAATAGT	10342
rs368491161	snp	C/T	1.66877e-05	0.00288852	intron-variant	TFG	GRCh38.p7	3:100744959	TGAAAGGGAGTTGGC[C/T]CATGGTTTTTTGTTT	10342
rs368538441	snp	C/G			intron-variant, upstream-variant-2KB	TFG	GRCh38.p7	3:100710617	GAACCAGAAGTTTGT[C/G]CGCCGAACCTAGAAC	10342
rs368696930	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100715663	TTCCTGTTTTCTTAT[A/G]CTTATCATACATTGA	10342
rs368807078	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100740938	TTATAATGGAGGTGA[A/G]AAATTTCTATTGCCT	10342
rs368907613	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100714656	TCTATTCTTATTTCC[C/T]GAAATGAAAGGTTTT	10342
rs368994316	snp	C/T	1.7022e-05	0.00291731	missense	TFG	GRCh38.p7	3:100748149	ATTTTGCCTTTTCAG[C/T]AAGCTATAGTCAGCA	10342
rs369040028	snp	A/T			intron-variant	TFG	GRCh38.p7	3:100728096	TCCTTGGCTTCCCAA[A/T]GTGGTGGGATTACAG	10342
rs369045243	snp	A/T			synonymous-codon	TFG	GRCh38.p7	3:100736703	AGCTCAGACTCAAGC[A/T]GGTCAGATTGAAGGT	10342
rs369059624	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	TFG	GRCh38.p7	3:100708073	AAACTAAATATGGCC[G/T]GAGAAGGACTCCATA	10342
rs369214559	snp	A/C			intron-variant	TFG	GRCh38.p7	3:100732240	AGCTTGTATTTTTTT[A/C]ATCTAATGTTTCTTA	10342
rs369343773	snp	A/G/T	1.65315e-05	0.00287498	synonymous-codon	TFG	GRCh38.p7	3:100713718	TCTAAGTGGGAAGCT[A/G/T]ATCATCAAAGCTCAA	10342
rs369409024	snp	C/T	1.64942e-05	0.00287173	synonymous-codon	TFG	GRCh38.p7	3:100728761	GGTGAAATATCTCCG[C/T]CGAGAACTGATAGAA	10342
rs369508900	snp	A/G	3.29962e-05	0.00406165	synonymous-codon	TFG	GRCh38.p7	3:100728752	ATCAAGTCAGGTGAA[A/G]TATCTCCGTCGAGAA	10342
rs369559199	snp	C/T	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100731930	TTTTAATAAGTAATA[C/T]ATATTAAAATAGAAG	10342
rs369615915	snp	A/C	8.27561e-05	0.00643205	intron-variant	TFG	GRCh38.p7	3:100736570	GACTTTTTTTTGACT[A/C]TCCAGGGCCACCCAG	10342
rs369701577	snp	A/G			upstream-variant-2KB	TFG	GRCh38.p7	3:100708974	CCTTTACACAGTTAC[A/G]GATTTTCCTTGCTCA	10342
rs369887753	in-del	-/T			intron-variant	TFG	GRCh38.p7	3:100737150	TAGTGGGTTTTTTTT[-/T]GTTAAGATTAGTAGC	10342
rs369922274	in-del	-/AGAC			intron-variant	TFG	GRCh38.p7	3:100713924	AAAAAAAAAAAAAAA[-/AGAC]AGAGCCTCTGTTGCC	10342
rs369981362	snp	A/G	4.98219e-05	0.00499084	missense	TFG	GRCh38.p7	3:100732649	TTATGTCAGCGTTTG[A/G]CTTAACAGATGATCA	10342
rs370226940	snp	A/C			intron-variant	TFG	GRCh38.p7	3:100743083	GATAATATATGCAAA[A/C]TGACTTTATAAACTA	10342
rs370243114	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100724614	AATTCATTTTGTGGG[A/G]TTAATATAACATTAA	10342
rs370273888	snp	C/G	8.23866e-05	0.00641767	missense	TFG	GRCh38.p7	3:100744849	TCAGATGTACCAACA[C/G]TACCAGCAACAGGCC	10342
rs370438736	snp	A/G	0.000204841	0.0101182	intron-variant	TFG	GRCh38.p7	3:100744977	TGGTTTTTTGTTTCT[A/G]TACTCATTAAACTTT	10342
rs370447670	snp	A/T			missense	TFG	GRCh38.p7	3:100732659	GTTTGGCTTAACAGA[A/T]GATCAGGTTTCAGGT	10342
rs370579431	snp	C/T	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100715817	CCTTTAACTCCTGTC[C/T]CCAGGCAATACTGCC	10342
rs370716880	in-del	-/G			intron-variant	TFG	GRCh38.p7	3:100745903	AACAGAAGACCATGT[-/G]GCCCACAAAGCCTAA	10342
rs370894142	snp	C/T	0.00119737	0.0244387	intron-variant	TFG	GRCh38.p7	3:100732388	TGTAATCCTATATTC[C/T]GACATGCTTAACATT	10342
rs371150426	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100738971	ATTTGGAACACTTCA[A/G]ACAACAAACAACATA	10342
rs371226161	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100719770	TGTAAATACCTTGCC[A/G]TAAGAGTAATAAGCA	10342
rs371285224	snp	A/C/T	6.84275e-05	0.00584885	utr-variant-5-prime	TFG	GRCh38.p7	3:100713674	TATATATAGAACATC[A/C/T]TGGAGTCCACCATGA	10342
rs371318665	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100730226	ACTGTTCAGAAATTA[A/G]CTACAGTGGCCCACA	10342
rs371412179	snp	A/G	1.65021e-05	0.00287241	synonymous-codon	TFG	GRCh38.p7	3:100736595	ACCCAGTGCTCCTGC[A/G]GAAGATCGTTCAGGA	10342
rs371420797	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100714021	TCCTGCCTCGGCCTC[C/T]CAAAGTGCTGGGATT	10342
rs371457918	in-del	-/A			intron-variant	TFG	GRCh38.p7	3:100716276	CTTGTATAAGATCAA[-/A]CTTTTTTTAGCTTCC	10342
rs371467052	snp	A/G	1.67601e-05	0.00289478	intron-variant	TFG	GRCh38.p7	3:100736525	TTCCTTGAGCTTGCT[A/G]GGGGAAGGCCTTGTG	10342
rs371474073	snp	C/T			utr-variant-3-prime, downstream-variant-500B	TFG, ABI3BP	GRCh38.p7	3:100748859	AGCCATCTTACTTGG[C/T]TTTTTACTATTAACA	10342
rs371598194	in-del	-/TTA			downstream-variant-500B	TFG, ABI3BP	GRCh38.p7	3:100749172	GGTTTAAAATGAACT[-/TTA]TTATTACTTCATAGG	10342
rs371617678	snp	A/T			intron-variant	TFG	GRCh38.p7	3:100729591	AAAACTCTTATTATT[A/T]TTTTTTTCTTTTTAC	10342
rs371681149	snp	C/T	4.9507e-05	0.00497504	missense	TFG	GRCh38.p7	3:100748334	GCCCAAACTTCTCAG[C/T]CTACTAATTATACTG	10342
rs371684906	in-del	-/T			intron-variant	TFG	GRCh38.p7	3:100734066	AGTTTTTTTTTTTGC[-/T]TTTTTTTTTTGCAAA	10342
rs371704682	in-del	-/G/TG/TGTG/TT	0.214098	0.253023	intron-variant	TFG	GRCh38.p7	3:100744807	CATGCCTTTTTTCCT[-/G/TG/TGTG/TT]TGTGTGTGTGTGTGT	10342
rs371789195	in-del	-/T			intron-variant	TFG	GRCh38.p7	3:100725620	CGTCTCTACCAAAAA[-/T]ACAAAAAAAAAAAAA	10342
rs371799325	snp	A/T			intron-variant	TFG	GRCh38.p7	3:100737400	TATTTAAAATAGGGG[A/T]TTGAAGGGCAACAGA	10342
rs371822732	snp	G/T			intron-variant	TFG	GRCh38.p7	3:100745336	CAGTTTACTATACAT[G/T]GAAAGGTGATGTTAT	10342
rs372174157	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100732122	AAAGCCTTAGTTCCT[A/G]TAATTATTTTTTCCA	10342
rs372196251	snp	C/T	3.37001e-05	0.00410474	intron-variant	TFG	GRCh38.p7	3:100732678	CAGGTTTCAGGTAAG[C/T]TGGTTTCCAACTCCT	10342
rs372197209	snp	A/G			upstream-variant-2KB	TFG	GRCh38.p7	3:100708078	AAATATGGCCTGAGA[A/G]GGACTCCATACATCT	10342
rs372286781	snp	A/G	0.000329799	0.0128371	synonymous-codon	TFG	GRCh38.p7	3:100736700	AGGAGCTCAGACTCA[A/G]GCAGGTCAGATTGAA	10342
rs372494286	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100732842	ATGTAAAAGACTAAC[C/T]AGATTAAGATGTAGA	10342
rs372641906	snp	C/T	6.74605e-05	0.00580738	synonymous-codon	TFG	GRCh38.p7	3:100748156	CTTTTCAGCAAGCTA[C/T]AGTCAGCAGACTGGA	10342
rs372850210	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100736264	AATTTTGGTTCCTGT[A/G]CAGAATACATTGCTT	10342
rs372931217	snp	A/G	3.45495e-05	0.00415615	intron-variant	TFG	GRCh38.p7	3:100732705	TCCTTTACACCCTTC[A/G]TTTCCTTCATCTTTC	10342
rs372946652	snp	C/G			intron-variant	TFG	GRCh38.p7	3:100735439	AGCCCATGCTATAAG[C/G]TCTTGTAAACTCATA	10342
rs373033831	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100740643	TCTAAGAATATAAAC[A/G]ATACCAACCCATTGT	10342
rs373139698	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100711139	GGAGTCTGGCTCTGT[C/T]GCCCAGGCTGTAGTG	10342
rs373148333	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100720362	ATTAGAATTTTTAAA[C/T]TGTAATTATCTTCCT	10342
rs373307369	snp	A/G	6.59729e-05	0.005743	missense	TFG	GRCh38.p7	3:100728763	TGAAATATCTCCGTC[A/G]AGAACTGATAGAACT	10342
rs373535747	snp	C/G	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100740058	CTAACAAGGTTCACA[C/G]TTTGCATTGTTAATG	10342
rs373541032	snp	A/C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100715021	ACTTACTTGCAGTGT[A/C/T]TTTAATCTTGACCTC	10342
rs373574068	snp	C/T			downstream-variant-500B	TFG, ABI3BP	GRCh38.p7	3:100749257	AGCCTGAATAAAACT[C/T]AGTGATTTTCCTTCT	10342
rs373703935	snp	C/T	0.000153988	0.00877328	utr-variant-5-prime	TFG	GRCh38.p7	3:100713665	CTAGAGTTGTATATA[C/T]AGAACATCCTGGAGT	10342
rs373719892	snp	A/G	3.31439e-05	0.00407073	missense	TFG	GRCh38.p7	3:100748482	CTTATGCGCGTAACC[A/G]TCCTCCCTTTGGTCA	10342
rs373760894	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100728237	CAGACCTATCAGTCA[C/T]GTTATATCTTTAAAC	10342
rs373972322	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100716156	TGCTATAGAACACTG[A/G]AACTACTTCTATCTA	10342
rs374000062	snp	C/G/T	3.40733e-05	0.00412741	intron-variant	TFG	GRCh38.p7	3:100728904	ATTGTTCTTACGTCT[C/G/T]TTTGGAGGTTTTAAA	10342
rs374006808	snp	A/G	0.000153988	0.00877328	synonymous-codon	TFG	GRCh38.p7	3:100744882	CTATGGTGCACAGCA[A/G]CCGCAGGCTCCACCT	10342
rs374039705	snp	A/G	0.00119737	0.0244387	intron-variant	TFG	GRCh38.p7	3:100727455	AACTTTTATTTTCAC[A/G]TAGATGTCCTTTTCT	10342
rs374056914	snp	A/G			upstream-variant-2KB, utr-variant-5-prime	TFG	GRCh38.p7	3:100709289	GAAAACCGGAAGTGC[A/G]TGGTCACGCCCCGCG	10342
rs374135579	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100744451	GAAGGACTTAGATGA[C/T]ATAAATGGTATTTGT	10342
rs374152144	snp	A/G	0.0023933	0.0345097	intron-variant, upstream-variant-2KB, utr-variant-5-prime	TFG	GRCh38.p7	3:100710075	CGTTTGGATTGAGAG[A/G]AGAGGGGCTTTGGGA	10342
rs374160782	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100725943	AGGGTTCTCCAGAGG[A/G]ATGGAACCAATAAGA	10342
rs374210483	in-del	-/A			intron-variant	TFG	GRCh38.p7	3:100713908	TTTTAAAGTCTTTTT[-/A]AAAAAAAAAAAAAAA	10342
rs374540797	snp	A/G	1.67534e-05	0.0028942	intron-variant	TFG	GRCh38.p7	3:100736529	TTGAGCTTGCTGGGG[A/G]AAGGCCTTGTGTTGG	10342
rs374592104	snp	G/T			intron-variant	TFG	GRCh38.p7	3:100714366	ATTAGCTGGGCGTGG[G/T]GGTGTGCGCCTGTAA	10342
rs374612559	snp	A/G	1.64963e-05	0.00287192	missense	TFG	GRCh38.p7	3:100732552	GCTTCTGATTCTTCT[A/G]GAAAACAGTCTACTC	10342
rs374837743	in-del	-/TAC			intron-variant	TFG	GRCh38.p7	3:100725620	CGTCTCTACCAAAAA[-/TAC]AAAAAAAAAAAAAAA	10342
rs375017002	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100718283	TCTCAAACTGACCTC[A/G]TTGACTGGCTTTCTC	10342
rs375301992	in-del	-/T			intron-variant	TFG	GRCh38.p7	3:100742526	CAACCCTGACAGGTT[-/T]GCTATTCCATTGCAG	10342
rs375313660	snp	A/C			intron-variant	TFG	GRCh38.p7	3:100712982	CAGGGACTGGAGGCC[A/C]GATGATTTTATAGGT	10342
rs375422548	snp	A/G	0.000153988	0.00877328	synonymous-codon	TFG	GRCh38.p7	3:100732605	TGCTTTTGATCCTTT[A/G]AAAAACCAAGATGAA	10342
rs375483576	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100713602	GCTCTCAACTTTTAC[A/G]GTATGTTTTGTTGTT	10342
rs375507112	snp	A/T			intron-variant	TFG	GRCh38.p7	3:100740738	TAAATAATTCCCAGA[A/T]GTCTTACCATTACTC	10342
rs375578333	snp	C/T	0.00119737	0.0244387	intron-variant	TFG	GRCh38.p7	3:100730501	GATGATAAGATGATA[C/T]AAGAATAATACAATC	10342
rs376052568	snp	C/G			upstream-variant-2KB	TFG	GRCh38.p7	3:100707934	TATTTCACTCTCAAA[C/G]AGAAGTTTCAGAGAC	10342
rs376064665	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100735609	GTCTAGCTCCAAAAC[C/T]TATGCTTTTAACCAC	10342
rs376065132	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100746037	TTTAGATTGTATTTG[C/T]TGTAGAGTGACTTAA	10342
rs376113336	snp	A/T			intron-variant	TFG	GRCh38.p7	3:100728369	AATTTAATAAATATT[A/T]AAGAACAGCATGAAA	10342
rs376176495	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100736922	AAAAAATACCTCAAA[A/G]AAGTGTTTCTATGAA	10342
rs376274130	snp	C/T	4.44336e-05	0.00471326	intron-variant	TFG	GRCh38.p7	3:100744810	TGCCTTTTTTCCTTG[C/T]GTGTGTGTGTGTGTG	10342
rs376385254	snp	C/G			intron-variant	TFG	GRCh38.p7	3:100714837	CCAGACTCATTTGTT[C/G]ACAAAATTATCTTTA	10342
rs376396150	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100733909	GTGAGGTAAAGGCAG[A/G]CAAAGGTTTTTAAAG	10342
rs376577330	snp	A/G	0.00199481	0.0315187	intron-variant	TFG	GRCh38.p7	3:100730181	AGAATATTAAGAAGT[A/G]TAGATGAGAATTTAA	10342
rs376602644	snp	A/G	0.00199481	0.0315187	intron-variant	TFG	GRCh38.p7	3:100720551	CACTTTGCATGTGCA[A/G]TTCACAATAGGGTTC	10342
rs376804190	snp	A/G	3.29794e-05	0.00406061	missense	TFG	GRCh38.p7	3:100728796	GAAATAAAGTGAATC[A/G]TTTATTGGATAGCTT	10342
rs376837970	snp	G/T			intron-variant	TFG	GRCh38.p7	3:100736766	TACATGTGTAGAAGT[G/T]TTTATTACAGCATTG	10342
rs376971794	snp	A/G	0.000164935	0.00907966	missense	TFG	GRCh38.p7	3:100728760	AGGTGAAATATCTCC[A/G]TCGAGAACTGATAGA	10342
rs377094635	snp	A/T	0.0217236	0.101931	intron-variant	TFG	GRCh38.p7	3:100728573	GAATTCTTTTTTTTT[A/T]AAAAAAAAGTTACTC	10342
rs377136610	snp	A/G	3.29717e-05	0.00406015	missense	TFG	GRCh38.p7	3:100713746	CAACTTGGGGAGGAT[A/G]TTCGGCGAATTCCTA	10342
rs377256112	snp	A/C			intron-variant	TFG	GRCh38.p7	3:100718974	GTTGTAGGATTCAGA[A/C]AAGAAAAAAAGAACA	10342
rs377277975	snp	A/G	0.000275962	0.0117433	intron-variant	TFG	GRCh38.p7	3:100744983	TTTGTTTCTATACTC[A/G]TTAAACTTTAAGTTC	10342
rs377381727	in-del	-/TG	0.198879	0.244718	intron-variant	TFG	GRCh38.p7	3:100744808	CATGCCTTTTTTCCT[-/TG]TGTGTGTGTGTGTGT	10342
rs377453870	snp	A/C/G			intron-variant	TFG	GRCh38.p7	3:100716274	TTACTTGTATAAGAT[A/C/G]AACTTTTTTTAGCTT	10342
rs377495804	in-del	-/C	0.00159617	0.0282053	utr-variant-3-prime	TFG	GRCh38.p7	3:100748585	TGGCCTCCCAAAAGA[-/C]CTCCAGTACTATTTT	10342
rs377646586	snp	A/G	0.000153988	0.00877328	missense	TFG	GRCh38.p7	3:100736584	TATCCAGGGCCACCC[A/G]GTGCTCCTGCAGAAG	10342
rs377690337	snp	G/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100726924	GGTGAGAGGAATGAA[G/T]CTTACTAAATCTTAT	10342
rs386397409	in-del	-/T			intron-variant	TFG	GRCh38.p7	3:100718550	CTTTGTATTTCATGG[-/T]TTTTTTTTTTTTTTT	10342
rs397700484	in-del	-/A	0	0	intron-variant	TFG	GRCh38.p7	3:100742901	ATGCAAAAAAAAAAA[-/A]GCTTTATGAAGAGTT	10342
rs397735838	in-del	-/A			intron-variant	TFG	GRCh38.p7	3:100744047	ATCTTTGCTTGAAAA[-/A]TCACAGGTATGGGAA	10342
rs397747466	in-del	-/T	0	0	intron-variant	TFG	GRCh38.p7	3:100711118	ATTTTTTTTTTTTTT[-/T]GAGACGGAGTCTGGC	10342
rs397767156	in-del	-/C	0	0	intron-variant	TFG	GRCh38.p7	3:100725678	GCGTGCCTGTAATCC[-/C]AGCCACTTGGGAGGC	10342
rs397803753	in-del	-/T	0	0	intron-variant	TFG	GRCh38.p7	3:100747353	AATCCTTTTTTTTTT[-/T]AATGCAGGGTTGTAC	10342
rs397876128	in-del	-/TT			intron-variant	TFG	GRCh38.p7	3:100745183	TAGTATAAAAAGTTT[-/TT]AATACAAAGCTGTCT	10342
rs397877549	in-del	-/C			intron-variant	TFG	GRCh38.p7	3:100726414	TCCTCTGGCAACACC[-/C]TCACAGACACACCCA	10342
rs398106214	in-del	-/AACA			downstream-variant-500B	TFG, ABI3BP	GRCh38.p7	3:100749218	GGACATAAACAAACA[-/AACA]GTAGATATAATGGGG	10342
rs527274305	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100726876	AGTAGAGATGATTCT[A/G]TGTTTGGGTATCTTA	10342
rs527286821	snp	A/T	0.00159617	0.0282053	intron-variant	TFG	GRCh38.p7	3:100719621	GGTAAAAGATGTAAA[A/T]TTTTTGGAATGAAAA	10342
rs527312655	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100726181	TACAAGCCCTGGAGT[C/T]CAAAGGCCAAAAAAC	10342
rs527588999	snp	A/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100739888	AATTGTGACAGGGTG[A/T]CACTCTGTTGCCCAG	10342
rs527672555	snp	C/T	0.0134861	0.0810011	intron-variant	TFG	GRCh38.p7	3:100711821	GCAAGATGGAATATT[C/T]ACCATCTTGGTGAAG	10342
rs527764234	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100746396	CAAAGCACATACAGC[C/T]ATTCAGTGGAGGGAG	10342
rs527920414	snp	A/G	0.00159617	0.0282053	intron-variant	TFG	GRCh38.p7	3:100723904	TTCCAGAAAATCCCA[A/G]AATGTAACAGATAAT	10342
rs527940043	snp	C/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100717959	AGACAGGGTCTTGCT[C/G]TGTCTCCCAAGCTGG	10342
rs528144404	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100738476	TGGGAATTAAGGCGC[C/T]ACTAGCAATATCTAA	10342
rs528224385	in-del	-/AAAC	0.0876117	0.190079	downstream-variant-500B	TFG, ABI3BP	GRCh38.p7	3:100749210	GTTAATTTAGGACAT[-/AAAC]AAACAGTAGATATAA	10342
rs528296910	snp	A/T			intron-variant	TFG	GRCh38.p7	3:100736269	TGGTTCCTGTGCAGA[A/T]TACATTGCTTGGAGT	10342
rs528299271	snp	C/T	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100716280	GTATAAGATCAACTT[C/T]TTTTAGCTTCCACAT	10342
rs528416162	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TFG	GRCh38.p7	3:100710581	CTGAAATTGAGCAGG[G/T]TCTTACCCTTAGAGG	10342
rs528484969	snp	A/C	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100722769	AAGTAGCATCCTATA[A/C]TCCACTAAATTTCAC	10342
rs528487596	snp	C/G			intron-variant	TFG	GRCh38.p7	3:100719534	ATCCATTCATTAAAG[C/G]AGTTTTGCAACAGTA	10342
rs528549004	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100715772	CTCATCCAGGCTACA[A/G]TGCAGTGGCATGATT	10342
rs528790559	snp	A/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100742973	GACCAGGAGTTCCTT[A/T]CTCATTGATGACCAC	10342
rs528921282	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100738656	CATTTAATTTTTAGA[A/G]TAGTATTGTATGCCT	10342
rs528950835	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100732427	TCATTATACACCTGC[A/G]TTATTTCCCTTGTAC	10342
rs528970040	in-del	-/AC	0.00119737	0.0244387	intron-variant	TFG	GRCh38.p7	3:100733233	TTTCGGATTCTAATA[-/AC]ACATACATTGGAGAG	10342
rs529090114	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TFG	GRCh38.p7	3:100710699	CCAGTGCTGAGAAAA[A/G]TGTACCTGGTAGAGG	10342
rs529097741	snp	C/T	0.00119737	0.0244387	intron-variant	TFG	GRCh38.p7	3:100740642	TTCTAAGAATATAAA[C/T]GATACCAACCCATTG	10342
rs529180362	snp	C/G	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100745582	TTAATGTAACTTTGG[C/G]TATAATTCCAGTATT	10342
rs529276198	snp	A/G	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100716412	TTCCATTGTGTATAT[A/G]TACCATATTTTCTTT	10342
rs529280610	in-del	-/GATT			intron-variant	TFG	GRCh38.p7	3:100716887	CCGATTTTAAAATCG[-/GATT]GATTGTTTTTTAGCT	10342
rs529294281	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100723794	GCAGGCTCAAACAGC[A/G]TTGGTCTTGTACATC	10342
rs529331503	snp	A/T	0.0023933	0.0345097	intron-variant	TFG	GRCh38.p7	3:100723476	TCTTAATGGAATTTT[A/T]AAAAAAATCCAGTTC	10342
rs529504871	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100743759	AAGCCTGTGAGTCCT[A/G]GCTGCCTACTGCAGC	10342
rs529618764	snp	G/T	0.00119737	0.0244387	intron-variant	TFG	GRCh38.p7	3:100729450	GTCAACATTTGGAAC[G/T]GACATAATTTTGGGA	10342
rs529634091	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	TFG	GRCh38.p7	3:100709292	AACCGGAAGTGCGTG[A/G]TCACGCCCCGCGCAT	10342
rs529671064	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100715617	TTTTGAGAGTTGCCC[A/G]TGTTAAGAAACAATA	10342
rs529828992	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100721872	GAATATAAAAGCAGC[C/T]GGCCGTGGTGGCTCA	10342
rs529952734	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100715016	GTGGAACTTACTTGC[A/G]GTGTATTTAATCTTG	10342
rs529996647	in-del	-/T			intron-variant	TFG	GRCh38.p7	3:100732287	ATTTTTTTGGAAAGC[-/T]TTTGTTCATCTTCTG	10342
rs530209377	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	TFG, ABI3BP	GRCh38.p7	3:100748893	TGTACTAAAGTAGAG[A/C]CCTTTGAGAATACAA	10342
rs530219173	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	TFG	GRCh38.p7	3:100707709	CTTAATGACATCATA[A/C]TACTATTATCTGACA	10342
rs530306790	snp	A/G	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100740669	ATTGTCATAAATGCT[A/G]TACATGTGCAGAAGC	10342
rs530375521	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	TFG	GRCh38.p7	3:100708259	AAGGCCAACGCCAAC[C/T]TGTAACCAATCCAGC	10342
rs530440281	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, utr-variant-5-prime	TFG	GRCh38.p7	3:100710011	CGCGCCTGGGGGGCT[C/G]CGGGAGGGGAGTGCG	10342
rs530532437	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100743911	ACATGTGATTATTTT[A/G]AAGATTTAAATACCA	10342
rs530620794	in-del	-/T	0.00438332	0.0466095	intron-variant	TFG	GRCh38.p7	3:100717410	GTAGTTCTGTACAAA[-/T]TTTATGGTTTGTTTT	10342
rs530817674	snp	A/G			downstream-variant-500B, utr-variant-3-prime	TFG, ABI3BP	GRCh38.p7	3:100749399	AATACAAAATGTAGC[A/G]TTGATAAGATTGAAG	10342
rs530870348	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100730659	CCTGTGGCTTACCCT[C/T]ACCAAGAAATGTGGC	10342
rs530973347	snp	A/G	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100735523	GGAAACTGAGGCACA[A/G]AAAGAGATTATGTAA	10342
rs530984317	snp	C/T			upstream-variant-2KB	TFG	GRCh38.p7	3:100708774	CCCTTGCCCCTGATA[C/T]TTCCTCTTAGTAATT	10342
rs530998240	in-del	-/TGAGTGATTTTCCTTCTCAGATAAAAGGTATAGTTGATT	0.497359	0.0362457	downstream-variant-500B	TFG, ABI3BP	GRCh38.p7	3:100749259	CTGAATAAAACTTAG[lengthTooLong]TGATTTTCCTTCTCG	10342
rs531085592	snp	C/T	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100734859	GAAGACCATTTTTCT[C/T]ACAGCTTTGTATGTT	10342
rs531178960	snp	G/T	0.00279162	0.0372561	downstream-variant-500B	TFG, ABI3BP	GRCh38.p7	3:100749234	GTAGATATAATGGGG[G/T]TTGGTAGAGCCTGAA	10342
rs531202710	snp	C/G	1.71349e-05	0.00292697	utr-variant-5-prime	TFG	GRCh38.p7	3:100713673	GTATATATAGAACAT[C/G]CTGGAGTCCACCATG	10342
rs531206126	snp	A/G	0.00119737	0.0244387	intron-variant	TFG	GRCh38.p7	3:100742233	TCACTTAACATTGTT[A/G]ATAGGTTCTTGGAAA	10342
rs531243169	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100741329	AAAATAGTGATATCA[A/G]TGATCCTGATGCTGT	10342
rs531261298	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	TFG	GRCh38.p7	3:100707854	TTATCCCTGCAAACA[A/G]TTGCTCAAAGGTCAA	10342
rs531442516	snp	A/G	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100740446	TGAGTAATCAGAAGA[A/G]AGTGAGGTAGAAGAT	10342
rs531446215	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100733477	ACATTCATTAAGTCT[A/G]TATTTTCCTTTAATT	10342
rs531634711	snp	C/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100733816	AAACAGAAAAGCGCT[C/G]TCTAAAAGAAAAAGG	10342
rs531673175	in-del	-/A	0.00438332	0.0466095	intron-variant	TFG	GRCh38.p7	3:100713436	ACAGTTAAATATGAG[-/A]AAAAATAATAGTAGA	10342
rs531687789	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100739922	GGAGTGTACTGGCTT[A/G]ATTACAGCTCACCTG	10342
rs531817689	snp	C/T	0.00159617	0.0282053	intron-variant	TFG	GRCh38.p7	3:100718015	TTGAAGCCTTGAACT[C/T]CTGGGCTCAAGCAGT	10342
rs531817740	snp	G/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100725169	CCTCGGCCTCCCAAA[G/T]TGCAGGGATTACAGA	10342
rs531861762	snp	C/T	0.00119737	0.0244387	intron-variant	TFG	GRCh38.p7	3:100711854	ATTATACTTTAGAGT[C/T]GGCACATAGTAGGTA	10342
rs531909665	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100721873	AATATAAAAGCAGCC[A/G]GCCGTGGTGGCTCAC	10342
rs532126868	snp	G/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100714981	ATTTTCTCTTTAGGT[G/T]GTTACCAGTGTTTTT	10342
rs532206104	snp	C/T	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100720618	ACAGGAGGCGGAGCC[C/T]ACCACTTAACCTCCT	10342
rs532210696	snp	A/G/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100734598	ACTTTCAGTTATTTC[A/G/T]AATAGTTTCTTTTGT	10342
rs532238545	snp	C/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100727132	TTGTGTGATGTTGGT[C/G]TTCTTTGAAATATTT	10342
rs532335103	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100727714	TTCATTAAAAAATCA[C/T]AACTAGAGATTACCG	10342
rs532417370	snp	A/C/G	0.00159617	0.0282053	intron-variant	TFG	GRCh38.p7	3:100739967	ATTCTTAATGTCAAC[A/C/G]TGTGCTAGTCTGTGT	10342
rs532439528	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100734018	TCTGAGGTTGGACAG[A/G]CAGTTTCTGGGCAGA	10342

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