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
rs532443375	snp	G/T	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100741196	AAGCTGTAGAACCAG[G/T]CTCAGATAGGTCCTT	10342
rs532477859	snp	A/G	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100740507	ACTGTCATTTCTGCA[A/G]TATTTTCTTGGTATA	10342
rs532637875	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100724017	GACAAAATATGGTTT[C/T]AAATAAGTCAAAGAA	10342
rs532820351	snp	C/T	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100718777	TGGCCAGGCTGGTCT[C/T]GAACTCCTGACCTCA	10342
rs532829609	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100726038	CTGCAAGCTGGGGAA[A/G]GAGAGAAGCTGATGC	10342
rs532999891	snp	A/T			intron-variant	TFG	GRCh38.p7	3:100721183	ATAATCTGAAGACCC[A/T]TACTTTAAACAGGAT	10342
rs533229324	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100731969	TTCAAAAATGTTTTT[A/G]ATGTGCTATTTATGG	10342
rs533236015	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100739293	GAGTTGTTACTTAAC[C/T]CCCATAAAAGGGACT	10342
rs533331565	snp	A/C	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100715490	CTTAGCACAACTTAT[A/C]CTGTGGAGGAGAAGT	10342
rs533359616	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100730705	GCTCTCTATTACAGC[A/G]GTTCTTGGATGCTTG	10342
rs533383804	snp	G/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100737660	CCAGAAGCAAGTGAT[G/T]AAGGTTATCAATTAC	10342
rs533385344	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100717170	AAAAGTCAGTTGGCT[A/G]TAGATAACATGGATT	10342
rs533495818	in-del	-/A	0.0622301	0.165053	downstream-variant-500B, utr-variant-3-prime	TFG, ABI3BP	GRCh38.p7	3:100749337	CAAAAACTCAATCTT[-/A]AAAAAAAACTACATC	10342
rs533568166	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100723565	GGAAAAGAGACTAGA[C/T]AAATGCAAAGAAAGC	10342
rs534084098	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100724878	TATCTCAATCATGTT[A/G]AAAAGTCGTAGCAAA	10342
rs534152867	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100737528	ATGAAGTGTGATTTT[C/T]GTATTGTCTATGTGT	10342
rs534268112	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100731209	TGATAATCATTGTCC[C/T]TTAATTGAGTAAATG	10342
rs534318421	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100745752	ATCAGCTAGAGCAGG[A/G]GTCAGTAAAGTATAG	10342
rs534400407	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100717218	GTGTTCTATTGATCT[A/G]TGTGTTTGTTCTCTT	10342
rs534667170	in-del	-/TT	0.00517822	0.0506191	upstream-variant-2KB	TFG	GRCh38.p7	3:100707591	TCAGGATCTGACCTC[-/TT]TTTAGTTTAAATATA	10342
rs534696907	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	TFG	GRCh38.p7	3:100708533	TCCACCTTAGAAGTG[A/G]CAAACATTCTCCGTT	10342
rs534696971	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100715236	GAGAAATCTTTCAGG[A/G]ATCCAGGTTGAAAGA	10342
rs534701398	snp	A/C			intron-variant	TFG	GRCh38.p7	3:100729649	TAGTTTAAAACTGTC[A/C]ATATTGTGAAATAGT	10342
rs534718539	snp	A/C	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100723279	GTATGCATGGTGTAC[A/C]TGTAAGAGTTATAAT	10342
rs534731722	snp	G/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100714772	TAGGAGTTTTCAGAT[G/T]ATGTAATATGCTTAT	10342
rs534744263	snp	C/T	0.00119737	0.0244387	intron-variant	TFG	GRCh38.p7	3:100722105	GCAGTGAGTCGAGAT[C/T]GCGCCACTGCACTCC	10342
rs535039096	in-del	-/AAC	0.00119737	0.0244387	intron-variant	TFG	GRCh38.p7	3:100735088	TATATTTAGGCTAAT[-/AAC]AGTGTCTTTTGTGGG	10342
rs535083115	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100734880	TTTGTATGTTGAATT[A/G]TAGTAGGAAAAACTG	10342
rs535121293	snp	G/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100723654	GATAAAAAGAATAAT[G/T]CACTAGGACTATATA	10342
rs535181861	snp	A/T	0.00159617	0.0282053	intron-variant	TFG	GRCh38.p7	3:100723974	ACTATTGGACAGAAT[A/T]TGTAACCCAAATTTC	10342
rs535463823	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	TFG	GRCh38.p7	3:100709109	GAATGAATGGATTTA[C/T]AGAAGAAAAGGTTTT	10342
rs535472200	snp	C/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100730986	TTTAAAGGAATACTT[C/G]TAGTAGTAGTTTTCT	10342
rs535507998	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100715845	GCCAACCCGGCCTCC[C/T]AAAGGCATAAGCCAC	10342
rs535534207	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100714184	GTTCCTATAGTTACT[A/G]TAATTCTCTCATCAG	10342
rs535596310	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100744353	TCTGGAACAAAAGAT[A/G]TCATATAGTTCCTTG	10342
rs535871566	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	TFG	GRCh38.p7	3:100709114	AATGGATTTATAGAA[A/G]AAAAGGTTTTTTCTT	10342
rs535941990	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100735740	ATATTCTCTCCATTC[A/G]TTTCTGTGTTCATTA	10342
rs535978348	snp	C/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100742366	ACCCCCAGACTTCTA[C/G]ATAAAGACTAAAAAC	10342
rs536049048	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100714494	GACACAGCAAGACTC[C/T]GTCTCAAAAAAAAAA	10342
rs536094517	snp	A/T	1.66807e-05	0.00288792	intron-variant	TFG	GRCh38.p7	3:100728869	AAATGGTAAACCCTG[A/T]ATCCATTGTATTCTG	10342
rs536162117	snp	A/G	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100722108	GTGAGTCGAGATCGC[A/G]CCACTGCACTCCAGC	10342
rs536168502	snp	C/T	0.00318978	0.0398085	utr-variant-3-prime	TFG	GRCh38.p7	3:100748813	CTAGCTTCCCTTGTC[C/T]GGAGGATATTAAAAT	10342
rs536190743	snp	A/C			intron-variant	TFG	GRCh38.p7	3:100729892	GATAGATGTTTAATA[A/C]ATATTTGGTGATTGA	10342
rs536195355	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100737544	GTATTGTCTATGTGT[A/G]TTGGGACCTTTAAAG	10342
rs536255800	snp	C/G			intron-variant	TFG	GRCh38.p7	3:100713573	AGAGTTTCTTAGCAT[C/G]TAATAGTAGCTTTGC	10342
rs536352581	snp	G/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100727241	ACCAGACCAGTTTCT[G/T]GCTGCTAGGAGCTGT	10342
rs536439793	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	TFG	GRCh38.p7	3:100708056	GTATCTGGTGTTAAA[A/G]CAAACTAAATATGGC	10342
rs536455791	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100724644	ACATGAAAACCAGCC[A/G]AGGAAAATGCAAACC	10342
rs536471724	snp	A/T			intron-variant	TFG	GRCh38.p7	3:100727650	TCATTTTTTTCAGTC[A/T]ACTGAAAATCATTTG	10342
rs536471836	snp	A/T	0.00119737	0.0244387	intron-variant	TFG	GRCh38.p7	3:100713907	TTTTTAAAGTCTTTT[A/T]AAAAAAAAAAAAAAA	10342
rs536501127	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	TFG	GRCh38.p7	3:100708404	CCAATTCGTGAAATC[A/G]TTCACTGCTCAATTA	10342
rs536514545	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100716151	TATAGTGCTATAGAA[C/T]ACTGGAACTACTTCT	10342
rs536656549	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100736425	AGCAAAGGAAAAAAT[A/G]AAGTACATACATTTA	10342
rs536673868	snp	A/G	1.64787e-05	0.00287038	missense	TFG	GRCh38.p7	3:100744842	TTTCAGGTCAGATGT[A/G]CCAACAGTACCAGCA	10342
rs536714219	snp	G/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100720699	GGGTTGGGGACCCTT[G/T]CTTTAGACAGTATTT	10342
rs536761688	snp	C/G	1.65677e-05	0.00287812	intron-variant	TFG	GRCh38.p7	3:100736568	CTGACTTTTTTTTGA[C/G]TATCCAGGGCCACCC	10342
rs536810167	snp	A/T			utr-variant-5-prime, upstream-variant-2KB	TFG	GRCh38.p7	3:100709327	GCATCGGGGCAGCTC[A/T]CGCTTCCTAAATCCC	10342
rs536846798	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	TFG	GRCh38.p7	3:100708997	CTTGCTCATAAACGC[A/T]GTAGGTCTTCCCTGC	10342
rs536932911	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100742522	GGGACCAACCCTGAC[A/G]GGTTGCTATTCCATT	10342
rs536970274	snp	C/T	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100740061	ACAAGGTTCACACTT[C/T]GCATTGTTAATGTGT	10342
rs536971928	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100741894	ACTGCTATGTACCAT[A/G]TAGCCTAGCTATGTA	10342
rs537042804	snp	C/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100714012	CTCAAGCAATCCTGC[C/G]TCGGCCTCCCAAAGT	10342
rs537044567	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100721467	ATTTTAGAAAAGTCT[A/G]CCTTGATACAGGGAA	10342
rs537081367	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100720720	GACAGTATTTCCCGA[A/G]GGGTACTTAAAGATT	10342
rs537085100	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100727989	AGGCATGTGCTGCCA[C/T]ACTTGGCTAATTTTT	10342
rs537106350	snp	A/T	0.00119737	0.0244387	intron-variant	TFG	GRCh38.p7	3:100714633	TTTTAGCTTAAAAAA[A/T]TTTTTTTTCTATTCT	10342
rs537132343	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100730085	TCAAGAATCAATGAA[A/G]AAGTTAGACAATTTT	10342
rs537138618	in-del	-/AT			intron-variant	TFG	GRCh38.p7	3:100746631	TATACACACACACAC[-/AT]GATAGAAGCATTGCC	10342
rs537160734	snp	C/T	0.000608231	0.0174283	intron-variant	TFG	GRCh38.p7	3:100728899	GACTTATTGTTCTTA[C/T]GTCTTTTTGGAGGTT	10342
rs537270619	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	TFG	GRCh38.p7	3:100708446	ATTTAATTCAGCTTA[A/C]GTTTTTCTTTTATAA	10342
rs537516377	snp	C/T	0.00398564	0.0444627	intron-variant	TFG	GRCh38.p7	3:100736512	TTAACCAAACTTATT[C/T]CTTGAGCTTGCTGGG	10342
rs537651097	snp	C/G			upstream-variant-2KB	TFG	GRCh38.p7	3:100708538	CTTAGAAGTGACAAA[C/G]ATTCTCCGTTTGGCC	10342
rs537690704	snp	A/G	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100740701	GTTGAGGGTCATGAT[A/G]GAGGTTGGCTACTCT	10342
rs537716471	snp	C/T	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100712093	GACCTTAGAGTGTTA[C/T]ATTTAGTTTTAATGA	10342
rs537723084	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100727395	TTCTAAAAGCTTATA[A/G]TTGGTGGTTTGATTT	10342
rs537758183	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100734217	TTTTGGTTTTGATAA[C/T]TTTCACATACTCAAA	10342
rs537874688	snp	A/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100713139	CTGGTTAGGAGTCTT[A/T]TCCAGTCATTTAGGC	10342
rs537924917	snp	A/T	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100740128	TTACATGTTTCTAAA[A/T]TCCCTTACATGTTTC	10342
rs537963070	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100732176	CTAGGATATAGGTTA[C/T]TGGGCTCCAAAAAAA	10342
rs538084991	snp	C/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	TFG	GRCh38.p7	3:100710970	TGTTTACTCTGGGGA[C/G]ATGACTGCAAGAGCA	10342
rs538171180	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100745255	AGTTTTCCCCCTTCC[C/T]TCCACCTCTCCATTT	10342
rs538313618	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100732865	GATGTAGATGATTTC[C/T]AGCACTTCAGAAAGC	10342
rs538453943	snp	C/G/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100742190	TTGGACTTGAATGAG[C/G/T]TGGGTTTAAAGTAAG	10342
rs538461731	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100747475	TTTCATGGTAGAGAT[A/G]AAAGTTTTCAGTGAA	10342
rs538539038	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100727156	AATATTTATATTCAA[C/T]GGGAGAACACCACAG	10342
rs538550553	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100748081	GTCCACCTAACAGTA[A/G]GACTAATTCTTTGGA	10342
rs538566254	snp	A/T			intron-variant	TFG	GRCh38.p7	3:100719161	AATCCAACTAATTAG[A/T]GTTAAAGTAGGTGCA	10342
rs538586137	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	TFG	GRCh38.p7	3:100748784	TACATGTATAAAGTG[A/G]TTGACTTGACTTTCT	10342
rs538721503	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100734336	AGCCTTCTTGAGATA[C/T]CCTCGTCTGCTCTCC	10342
rs538759301	snp	A/C	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100740945	GGAGGTGAAAAATTT[A/C]TATTGCCTAGTGATG	10342
rs538895694	snp	A/C	0.00517822	0.0506191	upstream-variant-2KB	TFG	GRCh38.p7	3:100707358	ACATAAAGAGCCTCA[A/C]GTTGCTTTCGGAGTC	10342
rs538966351	snp	C/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100739150	AGTCTTTGACATTGT[C/G]AGTTATTTAGATCAA	10342
rs539042172	snp	C/T	0.000798403	0.0199641	intron-variant, utr-variant-5-prime	TFG	GRCh38.p7	3:100711021	AGCACTGGTTCCTGG[C/T]CACAAGATGTTTACA	10342
rs539063438	snp	C/T	0.00199481	0.0315187	intron-variant	TFG	GRCh38.p7	3:100714424	AGAATTACTTGAACC[C/T]GGGAGGTGGAGCTTA	10342
rs539123305	snp	C/T	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100744522	GCTTTTAATGAACAT[C/T]AGCGTTACTTATCTG	10342
rs539146928	snp	G/T	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100737143	TTTAGTTGTAGTGGG[G/T]TTTTTTTGTTAAGAT	10342
rs539714977	snp	G/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB, utr-variant-5-prime	TFG	GRCh38.p7	3:100710169	GGAATAAGTTGATTG[G/T]GGTCATAGAATCGGA	10342
rs539738413	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100737229	CAGTGTATTTTAAGT[C/T]AGACTTTTTCTTCTG	10342
rs539769353	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100734668	TCTGATGGATTTACT[C/T]TGCCTTTATCAGTAG	10342
rs539860862	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, utr-variant-5-prime	TFG	GRCh38.p7	3:100710205	GTTCCTTGGCTAAGT[C/T]AGCGCTTAATCAAGC	10342
rs539928640	snp	A/C	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100731595	ATACACATTTCCGCC[A/C]CTCCTGTTACCCAGA	10342
rs539959475	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100744387	CCAAAGAGTTTGTTC[A/G]TATGGTAATAGAGGC	10342
rs539987066	in-del	-/AA			intron-variant	TFG	GRCh38.p7	3:100738557	AATGCGAAAGGACAT[-/AA]ACAGTGAAAATTCTC	10342
rs540056526	snp	C/G			intron-variant	TFG	GRCh38.p7	3:100717095	TTTTGAGGTCTTATT[C/G]ATGAAATCTTTTCCC	10342
rs540082426	snp	C/T	0.00199481	0.0315187	intron-variant, utr-variant-5-prime, upstream-variant-2KB	TFG	GRCh38.p7	3:100709567	CGCGATTGGCCGGGG[C/T]CCGCGCGAGCCTGCG	10342
rs540091753	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100716960	TCCTCTGCCAGATGA[A/G]TAGTTGTATTTCCTC	10342
rs540098278	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100716552	TTCCTTTAGTTAAAT[A/G]TTCAGTAGTGGCATC	10342
rs540117244	snp	A/T			intron-variant	TFG	GRCh38.p7	3:100742719	GTAACCCCAACTGGG[A/T]ATAATTTTTTTTTCC	10342
rs540157340	snp	C/T	0.00119737	0.0244387	intron-variant	TFG	GRCh38.p7	3:100731560	ACAGTTACCAACTTA[C/T]AGTATCATATAATTA	10342
rs540313858	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100739233	TTTGTTAACATAGCA[A/G]TCTCTTACAATGTGT	10342
rs540343777	snp	C/T	0.00119737	0.0244387	intron-variant	TFG	GRCh38.p7	3:100723768	CAATTATGGGAGAGC[C/T]GATAAATCAAGCAGG	10342
rs540513022	snp	A/T	0.00119737	0.0244387	intron-variant	TFG	GRCh38.p7	3:100716270	CTTTTTACTTGTATA[A/T]GATCAACTTTTTTTA	10342
rs540576655	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100738696	TAACTGTTAGCTTAC[A/G]TTAAAACATACAGTA	10342
rs540588745	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100737539	TTTTTGTATTGTCTA[C/T]GTGTGTTGGGACCTT	10342
rs540588851	snp	G/T	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100730020	TTCAGGTCAAAGAAG[G/T]TTGCCTATTCTGAGC	10342
rs540710035	snp	A/G	0.00358779	0.0422022	intron-variant	TFG	GRCh38.p7	3:100722496	AATTTTCAGAGTTAT[A/G]TAAAAGCTATAGACC	10342
rs540733157	snp	A/G	0.00199481	0.0315187	intron-variant	TFG	GRCh38.p7	3:100723443	AGAAATTGACTACAT[A/G]TATCGGTTAAAATAA	10342
rs540748916	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100730533	GCATTATATTTTTAG[A/G]GATAGTTCTTATTTT	10342
rs540785986	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100743051	CCAAGTTAATATTTA[C/T]ATTGTTTTGTTCATG	10342
rs540855291	snp	C/G	0.00159617	0.0282053	intron-variant, utr-variant-5-prime, upstream-variant-2KB	TFG	GRCh38.p7	3:100709784	CGGGAGACTAGGAGG[C/G]GCTGGGAGGGCCTCG	10342
rs540907540	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100729082	TCATCATAGACCTAC[C/T]GGAGCGTAGCACCTG	10342
rs541049186	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100730603	ACTGAAATCTAGTCC[A/G]CAAAATGAAATTGCC	10342
rs541063093	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	TFG	GRCh38.p7	3:100708200	GTCTTGGCCAATTCC[A/T]GCCGCCACACTTCAA	10342
rs541158434	snp	A/G	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100742067	CATTTTGCTCTCTTC[A/G]TATATCCTATAGATC	10342
rs541377237	in-del	-/AACA			downstream-variant-500B	TFG, ABI3BP	GRCh38.p7	3:100749215	TTAGGACATAAACAA[-/AACA]ACAGTAGATATAATG	10342
rs541564577	snp	G/T			intron-variant	TFG	GRCh38.p7	3:100711949	TTGTGTGGAGATTTC[G/T]GTTAATCACTGTCTT	10342
rs541576403	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100729136	TTTGGGTGATTCTTT[C/T]GCAACTAGTCTTAGA	10342
rs541673855	in-del	-/T	0.00795532	0.062565	intron-variant	TFG	GRCh38.p7	3:100720281	AGAGTGTTAAGTATG[-/T]TTTTTTTTGAAATCA	10342
rs541699925	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100723293	CATGTAAGAGTTATA[A/G]TTGAAAAATTAGACA	10342
rs541946821	snp	G/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100735992	CTTACTAGAAGTGTG[G/T]AATTATAATTGGATT	10342
rs541983665	snp	A/G	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100742694	GAATGTGCAGACTCT[A/G]CACAGAACAGTAACC	10342
rs542124577	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	TFG	GRCh38.p7	3:100708564	TGGCCAAACTTCGGG[C/T]TCCTGGGCCTTCTCC	10342
rs542254473	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100743874	TAATAGGTAGTTTGA[A/G]TATTTTTCAAAGAAT	10342
rs542402905	in-del	-/CTCT			intron-variant	TFG	GRCh38.p7	3:100747948	ATTATGTCTTAGAGA[-/CTCT]GTTTAAAAAATTGTA	10342
rs542414158	snp	A/T	0.00159617	0.0282053	intron-variant	TFG	GRCh38.p7	3:100747499	CAGTGAAGCAGACTT[A/T]CGTTGTAAAAAAAAT	10342
rs542469836	snp	C/G			intron-variant	TFG	GRCh38.p7	3:100733179	TTCTGTTTAACTTTT[C/G]GTTATAATTTCTTCA	10342
rs542485058	snp	A/T	0.00119737	0.0244387	intron-variant	TFG	GRCh38.p7	3:100721701	TCCAGGTCACATAGG[A/T]TTCTCACAGACAAAA	10342
rs542501635	snp	C/T			upstream-variant-2KB	TFG	GRCh38.p7	3:100708691	CATCCTCCACCACCC[C/T]CAGGTGATGTCTGCT	10342
rs542597936	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100726902	TCTTATCAAATCTTA[C/T]CTAGAAGGTGAGAGG	10342
rs542724844	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100720922	GCTGTTTTGTTGTTT[C/T]GTTTAGCATTAATTT	10342
rs542757673	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100727542	AGTTTAATTTTTGAA[C/T]GCCTGTCTTGGGGTT	10342
rs542762385	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100732399	ATTCCGACATGCTTA[A/G]CATTCCAGACTATCA	10342
rs542888864	snp	G/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100725833	CTTTAACAAAGATGG[G/T]TGTTTAGTAAGTTTA	10342
rs542926993	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100717811	TTTTGTTTATATAAG[A/G]TTATGTCATCTGCAA	10342
rs542927606	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100732993	TTAAAAATCTGAACT[A/G]TTTTATAATTTGATT	10342
rs543050972	snp	C/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100719213	CTTGTGGCCTCCCCA[C/G]GACAGAACTCCTCCC	10342
rs543108373	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100712662	TGTTGTAGACTCTGG[A/G]AATATGGAAAACATA	10342
rs543171160	snp	A/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100741164	AGAGTGTACTCCTAC[A/T]TATTTAAAAAAAAAC	10342
rs543391130	in-del	-/TCTTGTA	0.00358779	0.0422022	intron-variant	TFG	GRCh38.p7	3:100744715	GTTGAACAAATACTT[-/TCTTGTA]TATTGTTACTCTGTT	10342
rs543424740	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100725952	CAGAGGGATGGAACC[A/G]ATAAGATACATGGGA	10342
rs543507568	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, downstream-variant-500B	TFG, ABI3BP	GRCh38.p7	3:100748881	CTATTAACATGATGT[A/G]CTAAAGTAGAGCCCT	10342
rs543508975	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	TFG	GRCh38.p7	3:100708104	CATCTATACTTGAAT[C/T]CTTGTGGATGAACTG	10342
rs543542721	snp	A/G	0.000626422	0.0176867	missense	TFG	GRCh38.p7	3:100748376	TCTCAACCTGGAATG[A/G]CTCCAAGCCAACCTG	10342
rs543548304	snp	A/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100721731	ACCGTAAGACACATG[A/T]AGCTGTCAGGTAAGC	10342
rs543679063	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100720245	TTTTAAGAAAATGAT[A/G]GAAGTTTAATTCAGT	10342
rs543720032	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100734524	AGCTGCAGAGGTCAG[C/T]GCTTTTAATTCTTAT	10342
rs543727804	snp	C/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100712771	TGAAGAAAAATAAAG[C/G]AGGATAAGAAGATAA	10342
rs543794300	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	TFG	GRCh38.p7	3:100707582	TCTCCTGCCTCAGGA[C/T]CTGACCTCTTTTTAG	10342
rs543860232	snp	G/T			intron-variant	TFG	GRCh38.p7	3:100740825	TCTGTCATTGATTCT[G/T]TTTGAAAATATACAT	10342
rs544108900	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100711198	ACCTCCGCCTCCCGG[A/G]TTCAAGCGATTCTCC	10342
rs544167552	snp	A/T			intron-variant	TFG	GRCh38.p7	3:100722853	CCCTTGTTAAAATAA[A/T]TTTTAACAGTGGTCT	10342
rs544188432	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100747020	TTATTAAGAACTAAG[C/T]TTGCTCTTAATAAAT	10342
rs544297504	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100735358	GCTGATAATAGCAAG[C/T]ACTTATATGGAACTT	10342
rs544345933	snp	A/C	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100739756	TTGCTGGAGTAGTTT[A/C]AATCAAATTATGAAC	10342
rs544362448	snp	G/T	0.00119737	0.0244387	intron-variant	TFG	GRCh38.p7	3:100744548	ATCTGTTGGCAGCTG[G/T]GTTGGAAAACATTTG	10342
rs544403624	snp	A/G	0.0103295	0.0711199	intron-variant	TFG	GRCh38.p7	3:100714212	CAGTTAAAATTAGCT[A/G]AGTGGGGCCGGGCGC	10342
rs544406025	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100713116	GGCAAAGGTAAAAAG[C/T]AGGCAGACTGGTTAG	10342
rs544460636	snp	C/G	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100718316	AACTACTGTTTAGGG[C/G]AAAGGTCAGCAAACA	10342
rs544499188	snp	A/G	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100711634	AAGTCTTTAAATTCT[A/G]TATGTCAGGCACTTT	10342
rs544600764	snp	G/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100737606	GTGCTCTAACTATTT[G/T]TTTAACGGGTCAGAT	10342
rs544663798	snp	G/T			intron-variant	TFG	GRCh38.p7	3:100745552	ATTATATGTATTTAA[G/T]TATGATAAATATTAT	10342
rs544728466	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100724321	AGGATTAGTTAAGGA[A/G]AAACAAGGCACAAAT	10342
rs544843003	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100746327	TGGGTGTGGGACTCA[A/G]GCGTTTGCATTTTAT	10342
rs544971364	in-del	-/T	0.00159617	0.0282053	intron-variant	TFG	GRCh38.p7	3:100737553	ATGTGTGTTGGGACC[-/T]TTAAAGCCGCATTCC	10342
rs544974355	snp	A/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100733230	TCTTTTCGGATTCTA[A/T]TAACACATACATTGG	10342
rs544976244	snp	C/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100740213	TAGATACTTAGACAA[C/G]AAAAGTTAATTATCT	10342
rs544982423	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100718938	AGGTAAAGTTCCTGC[C/T]ATCAGAGATACTCTG	10342
rs545360680	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100724460	TAAATTTAATGTACT[A/G]TTTCAAGAAGTAGAA	10342
rs545390226	in-del	-/ACT	0.0023933	0.0345097	downstream-variant-500B, cds-indel	TFG, ABI3BP	GRCh38.p7	3:100749345	CAATCTTAAAAAAAA[-/ACT]ACATCTCTTTATTGC	10342
rs545398034	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100731361	CTTTCACAAGACAGT[A/G]GTATAAATGCCTGTG	10342
rs545431416	snp	C/T	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100725036	AGCTTCCCGAGTAGC[C/T]GGGACTACAGGCACC	10342
rs545433526	snp	C/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100739898	GGGTGTCACTCTGTT[C/G]CCCAGGTTGGAGTGT	10342
rs545466218	snp	C/T	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100717919	GCTTAACTGTCTTTT[C/T]TTTATTTTTTATTTT	10342
rs545490867	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100711665	TCTAGGTGCTGCTGG[A/G]AATAGATAGTACCAG	10342
rs545495293	snp	A/C	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100718434	ACCATTTTTCATTCA[A/C]AGACCTATAACAACA	10342
rs545523364	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100744776	ATCTTAAAAATATTT[C/T]TCTTTGCCACATTAA	10342
rs545599363	in-del	-/TACTA	0.00119737	0.0244387	intron-variant	TFG	GRCh38.p7	3:100741124	ACTCATTTGTGAATT[-/TACTA]TACTATATTTTTAAA	10342
rs545666308	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100716874	TTCAGATCATTTGCC[A/G]ATTTTAAAATCGGAT	10342
rs545704871	snp	G/T	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100716271	TTTTTACTTGTATAA[G/T]ATCAACTTTTTTTAG	10342
rs545728938	snp	C/T	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100723371	AGTAGAAAGTGGTGG[C/T]GGAATAAAAGAGGTA	10342
rs545848442	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100731621	CCAGAGTGGAGTACA[A/G]TCTCAGCTCACTACA	10342
rs546004672	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100733463	AGATTCTTTATTTTA[C/T]ATTCATTAAGTCTAT	10342
rs546066222	in-del	-/TT	0.00676609	0.0577691	downstream-variant-500B	TFG, ABI3BP	GRCh38.p7	3:100749129	GGTTTTTGCCCTTCC[-/TT]TTTGAAAAAAATGCA	10342
rs546072382	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100738404	GTATACTGTGATACA[A/G]TGACAGTTGGAAGGA	10342
rs546077061	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	TFG	GRCh38.p7	3:100709227	AAAGTTTAGAACAGC[A/G]CACTACGCCCCGCCC	10342
rs546154171	snp	G/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100730263	TCTAAGGAATGGATT[G/T]ATGAGTTTTTTGCTT	10342
rs546178392	snp	C/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100736231	GGTCAGTGAAGACCC[C/G]TTGAAGAATGAAGTG	10342
rs546337896	snp	A/C	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100736893	GTCAGGTATGTTTCC[A/C]ATTATTGGAATGAAA	10342
rs546513553	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100742808	GTAAAAGGAATCTTG[C/T]GTAGAGATATAATAA	10342
rs546575770	snp	C/T	1.64817e-05	0.00287064	intron-variant	TFG	GRCh38.p7	3:100744829	TGTGTGTGTGTGTTT[C/T]CAGGTCAGATGTACC	10342
rs546632734	snp	A/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100722783	ACTCCACTAAATTTC[A/T]CGAATGAGGAGAAGT	10342
rs546654441	in-del	-/ATT	0.00755907	0.0610114	utr-variant-3-prime	TFG	GRCh38.p7	3:100748679	TTAATTGAAAGTATA[-/ATT]ATTTGCTGGAACACA	10342
rs546738342	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	TFG	GRCh38.p7	3:100709017	GTCTTCCCTGCTTAA[C/T]TGGAAACTCCTTGCT	10342
rs546881634	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100742331	TTGAGTTCCTACAGC[A/G]TATCTCTGATCACAA	10342
rs547179052	snp	G/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100735694	GTCCTCAGAATATCT[G/T]TTTTGACTGTCACAG	10342
rs547265955	snp	A/G	0.00119737	0.0244387	intron-variant	TFG	GRCh38.p7	3:100722106	CAGTGAGTCGAGATC[A/G]CGCCACTGCACTCCA	10342
rs547343695	snp	A/G	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100736333	ATTTTTGCAGGGAGA[A/G]GTTAAGACTCAGGAA	10342
rs547345487	snp	C/G	0.000399281	0.0141238	downstream-variant-500B, utr-variant-3-prime	TFG, ABI3BP	GRCh38.p7	3:100749380	AATTTATACTTGTTT[C/G]AAAAATACAAAATGT	10342
rs547350616	snp	G/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100733622	CTCCCCCACACACAC[G/T]CCCCCCAACTCCAGT	10342
rs547548283	snp	G/T	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100746276	GGGAGGCTATGTGTG[G/T]GGCCCCATTCCCAGA	10342
rs547691065	snp	C/T	0.00119737	0.0244387	intron-variant	TFG	GRCh38.p7	3:100714436	ACCCGGGAGGTGGAG[C/T]TTACATTGAGCCAAG	10342
rs547754608	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100742426	GATTAATAAAAACAA[A/G]TAAGATAATGATTTA	10342
rs547876263	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100744675	CTTCTAAAATGGTTC[A/G]TTCTCTTCTTCATAG	10342
rs547917993	snp	A/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100743227	TACTAATATGGTTGA[A/T]TTTTTTTAAATGTGT	10342
rs547991906	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100724074	GTAGATAATGACTTC[C/T]ATGTAACCAAGTTTT	10342
rs548021591	in-del	-/AA	0.00199481	0.0315187	intron-variant	TFG	GRCh38.p7	3:100721076	TTAAATGTTAATAAC[-/AA]AAACTGTTTAAAATT	10342
rs548073663	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100736180	AAATAATGTTTGGAC[C/T]CTTAATGCCAAACTA	10342
rs548109303	snp	A/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100747748	TTATAGTATTATTTC[A/T]TATAAAAATGTTCAT	10342
rs548153419	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100726055	AGAGAAGCTGATGCT[A/G]ATAGTGGCTCAGTGG	10342
rs548210502	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	TFG	GRCh38.p7	3:100709312	GCCCCGCGCATGCGT[A/G]CATCGGGGCAGCTCA	10342
rs548226230	in-del	-/A			intron-variant	TFG	GRCh38.p7	3:100732345	TAGAAGGAAAAATAT[-/A]AAAAAAAATAAAGGA	10342
rs548248492	snp	A/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100734744	GGAATTACTCACAAA[A/T]GAGAATTGTGTGAAA	10342
rs548299421	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100727857	TAAAATTTTTTGAGA[C/T]AAGGTCTCCCTCTGT	10342
rs548412114	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100714566	GAACATTTTCACATA[C/T]ATTTTTTTTACAAGC	10342
rs548417339	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	TFG	GRCh38.p7	3:100707726	ACTATTATCTGACAG[C/T]AGTGCATCTCCCCAA	10342
rs548435417	in-del	-/AGA	0.00676609	0.0577691	downstream-variant-500B	TFG, ABI3BP	GRCh38.p7	3:100749025	AAGGAACAATTTTTC[-/AGA]AGAAGTCCTTATTGG	10342
rs548599953	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100741317	ATATGGAGGTGGAAA[A/G]TAGTGATATCAATGA	10342
rs548749561	snp	A/G	0.00119737	0.0244387	intron-variant	TFG	GRCh38.p7	3:100724035	ATAAGTCAAAGAAGA[A/G]ATAATAATGGGAATT	10342
rs548772203	snp	C/T	8.28164e-05	0.00643439	missense	TFG	GRCh38.p7	3:100748481	CCTTATGCGCGTAAC[C/T]GTCCTCCCTTTGGTC	10342
rs548783611	snp	A/G	0.00199481	0.0315187	intron-variant	TFG	GRCh38.p7	3:100713554	AATGAATCTTTTGGA[A/G]GCTAGAGTTTCTTAG	10342
rs548809582	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100747916	GAATTATGCTATGTC[A/G]GGAATTTGCTCTCAG	10342
rs548897973	snp	G/T	0.00159617	0.0282053	intron-variant	TFG	GRCh38.p7	3:100740676	TAAATGCTATACATG[G/T]GCAGAAGCCGTTGAG	10342
rs548917951	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100719662	TAAACCAACAATTTA[C/T]GATATTGCTCTCTAT	10342
rs548927183	snp	A/G			upstream-variant-2KB	TFG	GRCh38.p7	3:100707313	AAGACTTTACTGATG[A/G]CTTCGGGATGAAGCA	10342
rs548935532	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	TFG, ABI3BP	GRCh38.p7	3:100749171	TTGGTTTAAAATGAA[C/T]TTTATTACTTCATAG	10342
rs548990310	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100719025	TACATACTTTATTTT[C/T]TTTAAAAAATGTGTT	10342
rs549117251	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100720482	AAACTGGTTTCGTGT[A/G]AGACAGTTCTTCTAT	10342
rs549117878	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100724565	TAAATTATACAAACT[A/G]TTCAAGAGCATAGGC	10342
rs549160292	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100732781	ATGGTGAAGTGCACA[A/G]ATCTTAAGGGTTCTG	10342
rs549238508	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100719129	AATTCTCAGTTTTGT[C/T]ATCTTTGCCCAAAAT	10342
rs549247291	snp	A/G	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100739021	CATTTCAGGTGCTCA[A/G]TAGCCACATGTAGCT	10342
rs549260284	in-del	-/AAAGGTAA/AAAGGTAAGTACAGGGAAAGGTCCTTTCAAAAG	0.0111288	0.0738526	downstream-variant-500B, utr-variant-3-prime	TFG, ABI3BP	GRCh38.p7	3:100749421	GATTGAAGCATGTTG[lengthTooLong]AAAGGTAAGTACAGG	10342
rs549263866	snp	A/G	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100717280	TTGGTCTGTGGGTCC[A/G]TTTTTGTGCCAGTCC	10342
rs549289210	snp	A/G	0.0023933	0.0345097	intron-variant	TFG	GRCh38.p7	3:100726223	TGTCCAAGGGCAGGA[A/G]GAGTGGAAGCAAGCA	10342
rs549319927	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100725406	GTAGGGGAATGGGTT[C/T]TGAGGAAAGGTACTC	10342
rs549325801	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100733329	TGGGTGATTTCTGTT[A/G]AACTCTTCAAGGTCG	10342
rs549668803	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100717992	CGCAGTGGTGTGATC[A/G]TGGCTCATTGAAGCC	10342
rs549691397	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100742093	AGATCTCTCAAGTAT[A/G]TGAAGAAGTTCATCC	10342
rs549851401	snp	A/T	1.66877e-05	0.00288852	missense	TFG	GRCh38.p7	3:100713696	CCACCATGAACGGAC[A/T]GTTGGATCTAAGTGG	10342
rs549894599	snp	G/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100739929	ACTGGCTTGATTACA[G/T]CTCACCTGCAACCTC	10342
rs549912850	snp	A/G	0.00478085	0.0486577	intron-variant	TFG	GRCh38.p7	3:100714402	ACTACTCGGGAGGAT[A/G]AGGCAGAGAATTACT	10342
rs550006384	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100718705	TGGAATTATAGGCAC[A/G]CACCACCACACTCGG	10342
rs550123935	snp	A/C	0.00159617	0.0282053	intron-variant	TFG	GRCh38.p7	3:100719850	AAGTTTAAGGTTTCT[A/C]TGGGAGAGTCCAACT	10342
rs550135231	snp	A/T			intron-variant	TFG	GRCh38.p7	3:100736492	TATAGTACTTTTAGT[A/T]TCTTTTAACCAAACT	10342
rs550244435	snp	A/G	0.00358779	0.0422022	intron-variant	TFG	GRCh38.p7	3:100733592	TTGGAGTCAGTTTCT[A/G]TTGACTGGGTTCCTC	10342
rs550247950	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100718039	AAGCAGTCCTTGCAA[C/T]TCAGCCTCCCGTGTA	10342
rs550514605	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100718615	TAGGCTGGAGTACAG[C/T]GGGGTGATCTTGGCT	10342
rs550533366	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100745929	CCTAAACTATTTACT[A/G]TCTGGCTCTTTACAG	10342
rs550633066	snp	G/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100737910	AAAGATTTAAAAAAA[G/T]TAGCCAGGTGCTATG	10342
rs550694478	snp	A/G/T	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100739077	TAGATAAATATAGTC[A/G/T]TTATTTATAGATTCC	10342
rs550936668	in-del	-/A	0.385801	0.2099	intron-variant	TFG	GRCh38.p7	3:100738087	AAACAAACAAAGCCA[-/A]AAAAAAAAAAATCCA	10342
rs551039434	snp	C/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100711970	TCACTGTCTTCACGA[C/G]AAGTCCATTGTGAGA	10342
rs551039700	snp	A/G	0.00318978	0.0398085	intron-variant	TFG	GRCh38.p7	3:100716465	ACTTAGGTTGATTCC[A/G]TATCTTGACTATTGT	10342
rs551103450	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100717139	GGTTATCCTTTTCCT[A/G]ATGAGTGGTCTTGTC	10342
rs551116092	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100737038	CTTTATTTTGTGTTA[C/T]AGATGCTATTTTATC	10342
rs551167167	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100719519	AAGAATTTACTGTCT[A/G]TCCATTCATTAAAGC	10342
rs551175627	snp	G/T			intron-variant	TFG	GRCh38.p7	3:100730769	CCTTAGATAGAAGAT[G/T]GACCTGTTGCAGTAT	10342
rs551277682	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100723500	CCAGTTCCATGCTAC[C/T]TCCAAGAGACATAAA	10342
rs551311310	snp	A/C	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100725296	TATAAATGTAACTAA[A/C]ATACCTATTATAATT	10342
rs551378377	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100724796	ATTAGAAAATCACAT[A/G]CTATTTTCCATAAAA	10342
rs551468643	snp	A/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100718808	GGTGATCCGCCCACC[A/T]CAGCCTCCCAAACTG	10342
rs551557918	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100745710	GGTTGAATCTAGTCT[A/G]AATTCTATTTTATAG	10342
rs551623673	snp	A/G	0.00478085	0.0486577	intron-variant	TFG	GRCh38.p7	3:100745101	TTTTACATTAATATT[A/G]TAAATCAACATTTCA	10342
rs551761727	snp	A/G	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100743320	AGTTCATTGTTATGT[A/G]CTATACGTATTTATT	10342
rs551847451	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TFG	GRCh38.p7	3:100710738	ATACAAGTTAGAAGC[C/T]GAGTCATTTCTGGAC	10342
rs551905854	snp	A/G	0.00119737	0.0244387	intron-variant	TFG	GRCh38.p7	3:100730797	TATCTCCAGCAGCTA[A/G]TGGAGCAAGTAGTAG	10342
rs551986981	in-del	-/A	0.00119737	0.0244387	intron-variant	TFG	GRCh38.p7	3:100743363	TTTCTGTACCTACTT[-/A]ACCTTTTTATTTTAG	10342
rs552017175	snp	A/T			intron-variant	TFG	GRCh38.p7	3:100712179	CTAGAGATATTAATT[A/T]AAGGACTAGTTAGAT	10342
rs552038289	snp	C/G			intron-variant	TFG	GRCh38.p7	3:100733681	GTCTGATAGTGTTTG[C/G]TTGAAAACTAGACAT	10342
rs552088851	snp	C/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100717178	GTTGGCTATAGATAA[C/G]ATGGATTATGTTCTT	10342
rs552131078	snp	A/T			intron-variant	TFG	GRCh38.p7	3:100727033	AAAGGTTGTTTGGTC[A/T]TTTTTCTGGTGTGGT	10342
rs552237288	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100715121	GCTTAACCTAGTTTT[C/T]TTATCACTAACAGTT	10342
rs552397638	snp	C/T	0.00318978	0.0398085	upstream-variant-2KB	TFG	GRCh38.p7	3:100708999	TGCTCATAAACGCTG[C/T]AGGTCTTCCCTGCTT	10342
rs552544929	snp	A/G	0.00755907	0.0610114	intron-variant	TFG	GRCh38.p7	3:100735902	CAGAAATGCAAAGTA[A/G]AAGTCAGTATGAGTT	10342
rs552574986	snp	A/G	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	TFG	GRCh38.p7	3:100710915	GGATTTCCCCTTGAA[A/G]GGAAAGTTTTGTTGC	10342
rs552626098	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100722750	TAAAGAAAAATAACT[A/G]GAAAAGTAGCATCCT	10342
rs552659872	snp	C/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100723281	ATGCATGGTGTACAT[C/G]TAAGAGTTATAATTG	10342
rs552679536	snp	A/T	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100723627	CTTGAGTAGTAATAG[A/T]CACTTTATGATGATA	10342
rs552774613	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100741337	GATATCAATGATCCT[A/G]ATGCTGTATAGGCCT	10342
rs552846584	snp	A/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100729809	TTTTAGTTACAGTTT[A/T]AATAAAGATGTATTT	10342
rs552902616	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	TFG	GRCh38.p7	3:100708545	GTGACAAACATTCTC[C/T]GTTTGGCCAAACTTC	10342
rs553024709	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100716708	CAGCATTTGTTATTT[A/G]TCTTTTTGATAATAA	10342
rs553066212	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	TFG	GRCh38.p7	3:100709101	CCAATAATGAATGAA[C/T]GGATTTATAGAAGAA	10342
rs553106359	snp	A/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100743411	TCCGAAAGTTAGTTA[A/T]GAAGTACAATCCAGG	10342
rs553381753	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100714806	CATTTTCAGAAGTTA[A/G]TAGTATGCAGTGTTC	10342
rs553498792	snp	G/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100720885	TGATTATGTGAAAAA[G/T]AAAATGTGTACACTT	10342
rs553500490	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	TFG	GRCh38.p7	3:100748800	TTGACTTGACTTTCT[A/G]GCTTCCCTTGTCCGG	10342
rs553569290	snp	A/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100728180	GATCAGCTATTTTAG[A/T]TAGCTGTTTTTTTTC	10342
rs553661407	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100727157	ATATTTATATTCAAC[A/G]GGAGAACACCACAGC	10342
rs553922509	snp	C/T	0.00795532	0.062565	intron-variant	TFG	GRCh38.p7	3:100739169	TATTTAGATCAACTA[C/T]TGGTTATAATTTGAG	10342
rs553948522	snp	C/T	0.00119737	0.0244387	intron-variant	TFG	GRCh38.p7	3:100734340	TTCTTGAGATATCCT[C/T]GTCTGCTCTCCCAGC	10342
rs553999168	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100726400	CTCAAATGTCAGTGT[C/T]CTCTGGCAACACCCT	10342
rs554084006	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100739519	AAAATCATCAGAGAT[C/T]GGGAGATATTGCTGT	10342
rs554098922	snp	A/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100725713	ACATGAGAATTGCTG[A/T]ACCTGGGAGGCAGAG	10342
rs554106855	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100747036	TTGCTCTTAATAAAT[C/T]TAGTCAGGGTCTTCA	10342
rs554168192	snp	C/T			intron-variant, upstream-variant-2KB	TFG	GRCh38.p7	3:100710475	CAGGGTTTGAGGCCT[C/T]TTGGCATTCTTTAGA	10342
rs554203345	snp	A/T			intron-variant	TFG	GRCh38.p7	3:100742660	AAGTGCCCAGAGAAA[A/T]CCCACACAGACTTGG	10342
rs554236886	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100735070	GCCAAAGTAATAAAT[A/G]TATATATTTAGGCTA	10342
rs554283149	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100722187	GAACATAAGAGCAAG[A/G]TGCTATTGTATTATG	10342
rs554319956	snp	G/T			intron-variant	TFG	GRCh38.p7	3:100720083	AAACTTTCTAATGAA[G/T]TTACTATTTTATTCA	10342
rs554488770	snp	C/T	0.000399281	0.0141238	downstream-variant-500B, utr-variant-3-prime	TFG, ABI3BP	GRCh38.p7	3:100749454	AAGGTCCTTTCAGAA[C/T]GACTGCAACAGTGCA	10342
rs554500836	snp	C/T	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100720151	GACTCAGGTAAGCAA[C/T]AACTTATTCAAATAT	10342
rs554704665	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100721711	ATAGGTTTCTCACAG[A/G]CAAAACCGTAAGACA	10342
rs554837272	snp	A/C	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100740111	TAGCCATTAGAAAAA[A/C]CTTACATGTTTCTAA	10342
rs554842055	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100726469	AGGCATTCCTCACTC[C/T]AATCAAGCTGACACC	10342
rs554887602	snp	A/C			upstream-variant-2KB	TFG	GRCh38.p7	3:100707705	CCATCTTAATGACAT[A/C]ATAATACTATTATCT	10342
rs554901393	snp	C/T	0.00199481	0.0315187	intron-variant	TFG	GRCh38.p7	3:100735887	AAAGTGAGAGCTATT[C/T]AGAAATGCAAAGTAG	10342
rs555040159	snp	C/T	0.00318978	0.0398085	intron-variant	TFG	GRCh38.p7	3:100712044	ATAAGCATGGCATCC[C/T]TAGAGTGGAATGCAG	10342
rs555064687	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100713393	TTTTAGATATATTAA[A/G]AAAAATCTAAATGGT	10342
rs555156298	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100739639	TAAATATTGAAACAT[A/G]CATAGAATAATCAAC	10342
rs555229713	snp	A/G	0.00159617	0.0282053	intron-variant	TFG	GRCh38.p7	3:100717694	TTTATTTTTTATTGT[A/G]TGTGTATAGAAACAC	10342
rs555385974	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100746224	TCATCATTTAATCTC[A/G]GGATTTCGGTCCTCA	10342
rs555518087	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100714882	GAATGAAAAATGTTT[C/T]GGCAAACACACTGAG	10342
rs555538704	in-del	-/AACA			downstream-variant-500B	TFG, ABI3BP	GRCh38.p7	3:100749316	GAACCATTCAGAAAT[-/AACA]AACAAAAACTCAATC	10342
rs555619774	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100711573	TCGGATGTAAAAACT[A/G]ATCTATATTACAGCT	10342
rs555640434	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100742751	TCTCAGTGTTTTAAC[A/G]AAACAATGTCGAACA	10342
rs555680222	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100716949	CTGAATATTCATCCT[C/T]TGCCAGATGAGTAGT	10342
rs555894087	snp	A/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100732146	TTTTCCAGAGTGCCC[A/T]GTGGGTATCTGATAC	10342
rs555932615	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100731246	AACAGTCTTTTTGTT[C/T]ACTTGTTCGTGTTTT	10342
rs556146247	snp	G/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100739090	TCGTTATTTATAGAT[G/T]CCCAGCATGAATTAT	10342
rs556174854	snp	A/C			intron-variant	TFG	GRCh38.p7	3:100716276	ACTTGTATAAGATCA[A/C]CTTTTTTTAGCTTCC	10342
rs556175963	snp	G/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100748073	CATTTTTGGTCCACC[G/T]AACAGTAAGACTAAT	10342
rs556378675	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100725516	AGGTGCGGTGGCTCA[C/T]ACCTGTAATCCCAGC	10342
rs556459532	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100719912	TTTTTACTAGTTTAC[C/T]GCTTATACAAATCTG	10342
rs556482794	snp	G/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100738271	AACTAGAACAAACTA[G/T]AACTAAAGCAGATGT	10342
rs556485363	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100713170	AAGTGATGATGGTGG[C/T]TTGAATCAAGTTGAT	10342
rs556501312	snp	G/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100716810	TGATTTTGAGCATTT[G/T]TTCATATATTTATTG	10342
rs556661831	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100717520	TTTTAACAATATTTG[C/T]TCTTATATAAGCATG	10342
rs556691702	snp	A/G	0.00159617	0.0282053	intron-variant	TFG	GRCh38.p7	3:100718385	TTGTGGGTCACATAA[A/G]GCCTCTGTCTCATCT	10342
rs556697639	snp	A/C			intron-variant	TFG	GRCh38.p7	3:100739680	GTCATGTGGCTTCAA[A/C]ACTTACCAATATTTT	10342
rs556802342	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	TFG	GRCh38.p7	3:100710479	GTTTGAGGCCTCTTG[A/G]CATTCTTTAGAATAA	10342
rs556822753	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100714274	GGAGACCGAGGTAGG[C/T]GGATCATTTGAGGTC	10342
rs556849298	snp	A/G	0.00119737	0.0244387	intron-variant	TFG	GRCh38.p7	3:100729878	GGAATTATGTTAATG[A/G]TAGATGTTTAATAAA	10342
rs556886245	snp	C/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100736810	ATGTATTTAGTCATG[C/G]CTTAAACACAGGAAA	10342
rs556890022	in-del	-/T	0.00398564	0.0444627	intron-variant	TFG	GRCh38.p7	3:100740785	CTCTTTTCCCCTTAA[-/T]TTTTTTTATTACTTT	10342
rs556897242	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100711463	TCAGAAGGACATACC[A/G]TCAATTATCTTCAAA	10342
rs557088402	snp	G/T	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100737260	AAATAATCTGTCCTT[G/T]GATATGCAGTTTAGT	10342
rs557229022	snp	C/T			upstream-variant-2KB	TFG	GRCh38.p7	3:100708627	AGTTTCAGCAAAGAA[C/T]CTTGTTAAGGCAGTG	10342
rs557254318	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100730353	TATATTTTTTATACA[C/T]ACTGTTAGCTTTTTA	10342
rs557374799	snp	G/T			intron-variant	TFG	GRCh38.p7	3:100733217	TTCCTGCTTTTTCTC[G/T]TTTCGGATTCTAATA	10342
rs557388693	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100715337	ACAGAGTATGAAGAA[C/T]CATATGGGAGATTTT	10342
rs557419381	snp	C/T	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100718164	ACTCCTGGGCTCAAG[C/T]GATCCTCCTGCCTTG	10342
rs557443412	snp	A/T	0.00636936	0.0560724	intron-variant	TFG	GRCh38.p7	3:100711492	AAGCTGGAATTTTTT[A/T]CTTAATTAGGAGTGT	10342
rs557534599	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100743543	TTTTTTTCTTGTCAT[A/G]TTTGGGAATAGGATA	10342
rs557929660	snp	A/C			intron-variant	TFG	GRCh38.p7	3:100734834	AATATTAATATGATT[A/C]ACATTATTTGAAGAC	10342
rs557960913	snp	C/T	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100737546	ATTGTCTATGTGTGT[C/T]GGGACCTTTAAAGCC	10342
rs558022448	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100717622	CATCTTCTTGGTTAA[A/G]CTGCTTCCTAGATAT	10342
rs558104514	in-del	-/AACCAAATTCCTT	0.00159617	0.0282053	intron-variant	TFG	GRCh38.p7	3:100738594	ACCTCTGTCCACAGC[-/AACCAAATTCCTT]TTTTCAGAGGTAGCA	10342
rs558321856	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100737421	GGGCAACAGACTTCA[C/T]ACAGCAGGCACTAAG	10342
rs558464028	snp	A/T	0.00159617	0.0282053	intron-variant	TFG	GRCh38.p7	3:100742532	CTGACAGGTTGCTAT[A/T]CCATTGCAGGGTGCA	10342
rs558474966	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100714049	ATTACAGGCATGAAC[C/T]GCCATGCCTGACCTT	10342
rs558483062	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100721505	GAAGCTTAACTCTTA[C/T]ACCTTGGGCCGTCAG	10342
rs558497376	in-del	-/GAA	0.00358779	0.0422022	upstream-variant-2KB	TFG	GRCh38.p7	3:100708876	AGGTAAGGGAGAAGG[-/GAA]GAAGAGTACGTAGGA	10342
rs558624780	in-del	-/TGAT	0.0023933	0.0345097	utr-variant-3-prime, downstream-variant-500B	TFG, ABI3BP	GRCh38.p7	3:100748935	AAAATGTAACACTGA[-/TGAT]TGATAGGTTAATAAA	10342
rs558649342	snp	A/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100714634	TTTAGCTTAAAAAAA[A/T]TTTTTTTCTATTCTT	10342
rs558656792	snp	A/C	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100732918	AGTAGCACCCTCCCC[A/C]TTAAAGAATAAGCAC	10342
rs558673323	snp	C/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100715432	ACATGGCTTTGCTAA[C/G]ATGCAAATGGGTTGG	10342
rs558693573	snp	A/C/G			intron-variant	TFG	GRCh38.p7	3:100730251	CCCACATTCTACTCT[A/C/G]AGGAATGGATTTATG	10342
rs558814645	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100720747	GATTAAAAATAGTTC[C/T]GATAAAAACCAATAG	10342
rs559016130	snp	A/G	0.00119737	0.0244387	intron-variant	TFG	GRCh38.p7	3:100727434	GTTTAACAAAGAATC[A/G]CCCTGAACTTTTATT	10342
rs559073923	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100726738	ATGAATACCACGGAG[A/G]ACAATAGGATGTCTT	10342
rs559384039	snp	G/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100715009	TTTTACTGTGGAACT[G/T]ACTTGCAGTGTATTT	10342
rs559421216	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100721841	AAAGTTATTTAAGAC[A/G]TAGAAGAAGGAATAA	10342
rs559470070	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100734690	TATCAGTAGTTGGAA[A/G]TGTGTACAGTCCATT	10342
rs559511137	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	TFG, ABI3BP	GRCh38.p7	3:100749154	AATGCATTTGGTAAT[C/T]GTTGGTTTAAAATGA	10342
rs559594897	snp	A/C	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100722501	TCAGAGTTATATAAA[A/C]GCTATAGACCCTCAG	10342
rs559650544	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	TFG	GRCh38.p7	3:100707694	CCCATCCCAAACCAT[C/T]TTAATGACATCATAA	10342
rs559657895	snp	A/C	0.00159617	0.0282053	intron-variant	TFG	GRCh38.p7	3:100713493	CCCTACAGTAAAATA[A/C]TGTTGCCTCCAGACC	10342
rs559696194	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100720431	ACATGTAAGTCTGAT[A/G]CTTGAAACCAGTAGT	10342
rs559819002	snp	A/T	0.00199481	0.0315187	intron-variant	TFG	GRCh38.p7	3:100717647	AGATATTTAAAAAAA[A/T]TTTTGTAGCTGTGGT	10342
rs559819211	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100721493	GGGAAAGTCAAGGAA[A/G]CTTAACTCTTATACC	10342
rs560023297	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100714173	TTGAATGTGATGTTC[C/T]TATAGTTACTATAAT	10342
rs560077242	snp	C/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100747245	CTCTGACCTTTTCCA[C/G]TTTTGTTCATGGACT	10342
rs560196123	snp	A/C			intron-variant	TFG	GRCh38.p7	3:100714913	TAGAATTATAGTAGT[A/C]GACTGTATTTCCTAT	10342
rs560201567	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100733264	GCTTGATACTGTCTC[A/G]TGGGTCATTAAGGTT	10342
rs560226768	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100719550	AGTTTTGCAACAGTA[A/G]TGTTTTACTCTACCT	10342
rs560238140	snp	A/C	0.00119737	0.0244387	intron-variant	TFG	GRCh38.p7	3:100739815	ATATGTCCAACTGAT[A/C]ATCTTCTTTTTAATA	10342
rs560256667	snp	A/C			upstream-variant-2KB	TFG	GRCh38.p7	3:100707686	GGTTTTACCCCATCC[A/C]AAACCATCTTAATGA	10342
rs560291570	snp	C/T	0.00119737	0.0244387	intron-variant	TFG	GRCh38.p7	3:100731536	CCCAGAAACCCACAT[C/T]CAGTTTCAACAGTTA	10342
rs560465412	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100740313	TTGCAGTTAAAAATG[A/G]CTGCTGGGGTTATAG	10342
rs560482524	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100711282	TCATTTTTGTATTTT[C/T]AGTAGAGACAGGGTT	10342
rs560506320	snp	G/T			intron-variant	TFG	GRCh38.p7	3:100715575	TTTGTTTTTGTGATG[G/T]GTAGTCTAAGAATAC	10342
rs560542666	snp	A/T	0.00199481	0.0315187	intron-variant	TFG	GRCh38.p7	3:100717923	AACTGTCTTTTTTTT[A/T]TTTTTTATTTTTTTG	10342
rs560548416	in-del	-/CAT/CATCT	0.0103295	0.0711199	downstream-variant-500B, utr-variant-3-prime	TFG, ABI3BP	GRCh38.p7	3:100749348	CTTAAAAAAAAACTA[-/CAT/CATCT]CATCTCTTTATTGCA	10342
rs560907262	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100740414	GGTGACCTCATGACA[C/T]GACAGCTTCACCAGA	10342
rs560928587	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100747959	AGAGAGTTTAAAAAA[C/T]TGTAGAGAATGCCTC	10342
rs561001770	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100720958	TTTTTTAATTTTGTT[A/G]CATGAAACTTAGAGT	10342
rs561003438	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100747501	GTGAAGCAGACTTTC[A/G]TTGTAAAAAAAATTA	10342
rs561074805	snp	C/T	0.00119737	0.0244387	intron-variant	TFG	GRCh38.p7	3:100733812	TAACAAACAGAAAAG[C/T]GCTCTCTAAAAGAAA	10342
rs561083791	in-del	-/T	0.00119737	0.0244387	intron-variant	TFG	GRCh38.p7	3:100741782	TATTTTCACTGTACC[-/T]TTTTTTATGTTTTGA	10342
rs561114854	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100725107	GAGACGGGGTTTCAC[C/T]GTGTTAGCCAGGATG	10342
rs561119543	snp	G/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100733451	GTTTTTCTGTTGAGA[G/T]TCTTTATTTTACATT	10342
rs561153548	snp	C/T	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100732426	ATCATTATACACCTG[C/T]ATTATTTCCCTTGTA	10342
rs561156256	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100739914	CCCAGGTTGGAGTGT[A/G]CTGGCTTGATTACAG	10342
rs561497809	in-del	-/T	0.0850919	0.187897	intron-variant, upstream-variant-2KB, utr-variant-5-prime	TFG	GRCh38.p7	3:100709468	AGGGGCGAAAGGACA[-/T]TTTTTTTTTTCTTGC	10342
rs561545686	in-del	-/AAAC/AAACAAAC	0.447968	0.19333	downstream-variant-500B	TFG, ABI3BP	GRCh38.p7	3:100749213	ATTTAGGACATAAAC[-/AAAC/AAACAAAC]AAACAGTAGATATAA	10342
rs561625148	snp	C/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100711836	TACCATCTTGGTGAA[C/G]TAATTATACTTTAGA	10342
rs561663430	snp	A/G	0.00119737	0.0244387	intron-variant	TFG	GRCh38.p7	3:100718675	TGATTCTCCTGCCTC[A/G]GCCTCCCAAGTAGCT	10342
rs561708150	snp	C/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100738641	AACACTGTTTATATG[C/G]ATTTAATTTTTAGAG	10342
rs561739143	in-del	-/CTT			intron-variant	TFG	GRCh38.p7	3:100716085	ACATTCAATATTCTC[-/CTT]CTAGCTATTTGAAAT	10342
rs561744783	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100745526	TCTATTTTACCATCT[A/G]TCCACTGAAGATTAT	10342
rs561791332	snp	C/T	9.88631e-05	0.00703006	synonymous-codon	TFG	GRCh38.p7	3:100744864	GTACCAGCAACAGGC[C/T]GGCTATGGTGCACAG	10342
rs561840485	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100718522	GTAGTTTGTCTTCCA[C/T]ATTTAGTTACAACTT	10342
rs561846127	snp	A/C	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	TFG	GRCh38.p7	3:100710525	GCTTAGTATTTCTTG[A/C]AGGAAACTGCTCCCC	10342
rs561904697	snp	A/G	0.000214195	0.0103466	missense	TFG	GRCh38.p7	3:100744865	TACCAGCAACAGGCC[A/G]GCTATGGTGCACAGC	10342
rs561914739	snp	G/T			intron-variant	TFG	GRCh38.p7	3:100715975	AATTGTACATATTTA[G/T]GGGGTACATAGTAAT	10342
rs561945054	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100739020	ACATTTCAGGTGCTC[A/G]ATAGCCACATGTAGC	10342
rs561979573	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100720575	AGGGTTCACACTCCT[A/G]TGTGAATCTAATGCC	10342
rs562035741	snp	C/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100730625	GAAATTGCCAATCAG[C/G]TATCAGTGCTATTTA	10342
rs562046423	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100735232	TTATATCCTAGTTTA[A/G]GTTCTTATTAATACT	10342
rs562111811	snp	G/T			intron-variant	TFG	GRCh38.p7	3:100734987	GGCAGTGGGAAGGAG[G/T]GATAAAATATTACAA	10342
rs562124673	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100736445	ACATACATTTAATGT[A/G]AAAAGGCGTATTTGT	10342
rs562206606	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100717028	CTTTGCTGTGCAGAA[A/G]AGTTTTCCAGTTTGA	10342
rs562216989	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100728290	GTATTATTTTAAGAA[C/T]AGCGTGAAATAAAAT	10342
rs562293232	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100743732	AATAGAGTGGGCTCC[A/G]TCTCATTTTCTAAGC	10342
rs562445618	snp	G/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100739768	TTTAAATCAAATTAT[G/T]AACAGCTTATTATAC	10342
rs562488074	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100733111	GCTTGAGTATACAGT[A/G]GGTTTTTATATAAAT	10342
rs562493927	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100718201	CAAAGTACTGAGATT[A/G]CAGGCATGAGCCAGT	10342
rs562634215	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100711646	TCTATATGTCAGGCA[C/T]TTTTCTAGGTGCTGC	10342
rs562664884	snp	A/T	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100745684	AACTGTAATTAGAAA[A/T]AATTTATGCAGGTTG	10342
rs562726242	snp	G/T	0.00159617	0.0282053	intron-variant	TFG	GRCh38.p7	3:100746277	GGAGGCTATGTGTGG[G/T]GCCCCATTCCCAGAG	10342
rs562744211	snp	A/G	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100731319	TCCTATTTGTAAAAT[A/G]TATGTTAAAATTCTT	10342
rs562762020	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100744613	GTTGCACTTAATGTT[C/T]ATTGCCAGTTAGTTC	10342
rs562835672	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100717163	TCTTGTCAAAAGTCA[A/G]TTGGCTATAGATAAC	10342
rs562837623	snp	G/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100724356	AATGTTAGAAATGAA[G/T]TTTATAGTAGAAACT	10342
rs562872300	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100723830	GTTAGGGAGAAATAC[A/G]GTTTTTTTTTTTTTC	10342
rs562897632	snp	A/C	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100713199	ATAGCAGTGAAGGTG[A/C]TGAAGTGGTTGGACC	10342
rs562956363	snp	A/G	0.00358779	0.0422022	intron-variant	TFG	GRCh38.p7	3:100737118	TTTCTGAATAGAGGT[A/G]AAGGATAACTTTAGT	10342
rs562989473	snp	C/G	0.0134861	0.0810011	intron-variant	TFG	GRCh38.p7	3:100711221	GATTCTCCTGCCTCA[C/G]TCTCCTGAGTATCTG	10342
rs563076150	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100737618	TTTGTTTAACGGGTC[A/G]GATAGTGGTATAATG	10342
rs563115789	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100722673	AAACAATTAGACTGT[C/T]AGTAGACTTCTTCAT	10342
rs563152131	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100721938	GGCGGATTGCCTGAG[C/T]GCAGGAGTTCGCGAC	10342
rs563178841	in-del	-/A	0.00119737	0.0244387	upstream-variant-2KB	TFG	GRCh38.p7	3:100709283	TTTCGAGAAAACCGG[-/A]AGTGCGTGGTCACGC	10342
rs563238418	snp	C/T	0.00159617	0.0282053	intron-variant	TFG	GRCh38.p7	3:100730701	TTCAGCTCTCTATTA[C/T]AGCGGTTCTTGGATG	10342
rs563239525	snp	C/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100716252	CTACTGTCATCTGTT[C/G]TGCTTTTTACTTGTA	10342
rs563279738	snp	A/G	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100723341	AAAAAGAAAACAAGG[A/G]TACCTGTTCAGTTCA	10342
rs563279746	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100715662	TTTCCTGTTTTCTTA[C/T]GCTTATCATACATTG	10342
rs563373031	in-del	-/A	0.00119737	0.0244387	intron-variant	TFG	GRCh38.p7	3:100726913	CTTATCTAGAAGGTG[-/A]GAGGAATGAATCTTA	10342
rs563508042	snp	C/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100729163	TAGACTTTTGGATTT[C/G]TTACACAGGTCAGTT	10342
rs563642047	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100723939	TATCTTAAAGGTCAT[A/G]TTCTCTGGCTTCTTT	10342
rs563655938	snp	A/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100742754	CAGTGTTTTAACGAA[A/T]CAATGTCGAACAAAA	10342
rs563672032	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100728593	AAAAGTTACTCCATT[A/G]CATTGATATCTTGTT	10342
rs563690369	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	TFG	GRCh38.p7	3:100708289	CTGTTTCTGTACTTC[A/G]CTGCCAATTTCTGTA	10342
rs563796291	snp	C/G			intron-variant, utr-variant-5-prime, upstream-variant-2KB	TFG	GRCh38.p7	3:100709803	GGGAGGGCCTCGTTC[C/G]AACCGCGCGGCAGCT	10342
rs563851198	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100736065	TATATGGGATCTAGT[A/G]GGAGAGAAATAGAGG	10342
rs563865777	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	TFG, ABI3BP	GRCh38.p7	3:100749194	CTTCATAGGATGAAA[A/G]GTTAATTTAGGACAT	10342
rs563867321	snp	A/G	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100714888	AAAATGTTTCGGCAA[A/G]CACACTGAGTAGAAT	10342
rs563927440	snp	C/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100741327	GGAAAATAGTGATAT[C/G]AATGATCCTGATGCT	10342
rs563976982	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100745330	TATGAACAGTTTACT[A/G]TACATGGAAAGGTGA	10342
rs564012100	snp	C/T			upstream-variant-2KB	TFG	GRCh38.p7	3:100708768	GAATCTCCCTTGCCC[C/T]TGATATTTCCTCTTA	10342
rs564069655	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, utr-variant-5-prime	TFG	GRCh38.p7	3:100710123	GCCCAATACCCGAAG[A/G]AGCTCGGAAGGGTGT	10342
rs564093843	snp	A/G	0.00517822	0.0506191	intron-variant	TFG	GRCh38.p7	3:100714374	GGCGTGGTGGTGTGC[A/G]CCTGTAATCCCAACT	10342
rs564231555	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100736017	TGGATTTTAAATAAT[A/G]TTATATTTAAATATG	10342
rs564376512	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100733493	TATTTTCCTTTAATT[A/G]TTTGAATGTATTTAT	10342
rs564392883	snp	A/T			intron-variant	TFG	GRCh38.p7	3:100738492	ACTAGCAATATCTAA[A/T]CATTCTATGAAGTGT	10342
rs564449085	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100736894	TCAGGTATGTTTCCA[A/G]TTATTGGAATGAAAA	10342
rs564484825	snp	G/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100736240	AGACCCCTTGAAGAA[G/T]GAAGTGACAATTTTG	10342
rs564642052	snp	G/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100729948	AGAACATAATGGAGA[G/T]TTGCTGAATACTATA	10342
rs564700668	snp	C/T			intron-variant, upstream-variant-2KB, utr-variant-5-prime	TFG	GRCh38.p7	3:100710238	CGGCTGGAGGCCCAG[C/T]CTGGTTTATAGTGAT	10342
rs564722084	snp	A/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100742864	ATGTTTTTCAAAATC[A/T]ATTTATAGCAGTTTA	10342
rs564751750	snp	C/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100741184	TAAAAAAAAACAAAG[C/G]TGTAGAACCAGGCTC	10342
rs564963407	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	TFG	GRCh38.p7	3:100708753	GTGTTGGTTTAGCCA[C/G]AATCTCCCTTGCCCC	10342
rs564990969	snp	A/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100740470	AGAAGATAACCTTTT[A/T]TAGCCTGTCCTCAGA	10342
rs564998300	snp	C/G	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100714958	TCTTTGTTAATATCT[C/G]TGCTGAAATTTTCTC	10342
rs565076194	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100727698	GTGAAGTAATGTTGC[C/T]TTCATTAAAAAATCA	10342
rs565101208	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100719505	GGTCAGTGACCTGAA[A/G]GAATTTACTGTCTAT	10342
rs565265876	snp	A/C	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100712825	AGATGGTTAGGAAAG[A/C]TCTCTCTCAGTTAAC	10342
rs565435433	in-del	-/T			intron-variant	TFG	GRCh38.p7	3:100746203	GCAGAGCTGAAGAGA[-/T]TTTAGTCATCATTTA	10342
rs565573002	snp	C/T	0.000798403	0.0199641	downstream-variant-500B, utr-variant-3-prime	TFG, ABI3BP	GRCh38.p7	3:100749398	AAATACAAAATGTAG[C/T]GTTGATAAGATTGAA	10342
rs565601894	snp	A/G			utr-variant-3-prime	TFG	GRCh38.p7	3:100748580	AGCTATTGGCCTCCC[A/G]AAAGACTCCAGTACT	10342
rs565723610	snp	A/G	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100726409	CAGTGTCCTCTGGCA[A/G]CACCCTCACAGACAC	10342
rs565826890	in-del	-/T	0.0372634	0.131313	intron-variant, upstream-variant-2KB, utr-variant-5-prime	TFG	GRCh38.p7	3:100710268	GATTCTAGCTAACTT[-/T]TAAGAGTTTGCTTTG	10342
rs565837446	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100721283	TATCCAGGGAACAAA[A/G]AAGTAGAGGGAACTA	10342
rs566014079	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	TFG	GRCh38.p7	3:100708055	AGTATCTGGTGTTAA[A/C]GCAAACTAAATATGG	10342
rs566139220	snp	A/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100747820	CCCCTGAAAACCTGG[A/T]TAATGACTATTTAGC	10342
rs566177508	snp	A/C	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100733658	CACATTTTTCTGTTT[A/C]TTTGCCTGTCTGATA	10342
rs566182700	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100746311	TTGAATTTCATTTGA[C/T]TGGGTGTGGGACTCA	10342
rs566191548	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100722296	AGTGGATAGGTTAAA[C/T]ACATTAGTCATAGCT	10342
rs566224935	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100713062	CTAGGTTTTACTTAA[C/T]AGTGTTAACTCTGGT	10342
rs566265156	in-del	-/TGGG			intron-variant	TFG	GRCh38.p7	3:100733314	CTCTGTTCTTCAGGT[-/TGGG]TGATTTCTGTTGAAC	10342
rs566297672	snp	G/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100746911	ATGTAGAGGATAGGA[G/T]AACTTGTATGACATT	10342
rs566471137	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100718229	AGTGTGCCTGGCCTT[C/T]AACTGCCTTTTTTCC	10342
rs566658520	snp	C/T	0.0023933	0.0345097	intron-variant	TFG	GRCh38.p7	3:100732112	TTTATAAAATAAAGC[C/T]TTAGTTCCTATAATT	10342
rs566694870	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100738984	CAAACAACAAACAAC[A/G]TATCACATTTCAAAC	10342
rs566806353	snp	A/G	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100724862	AAAGAAAAGCCATTC[A/G]TATCTCAATCATGTT	10342
rs566819958	snp	C/T	6.81385e-05	0.00583649	intron-variant	TFG	GRCh38.p7	3:100732691	AGTTGGTTTCCAACT[C/T]CTTTACACCCTTCGT	10342
rs566840197	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100739280	AATTAAGAATTCTGA[A/G]TTGTTACTTAACTCC	10342
rs566855870	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100745115	TGTAAATCAACATTT[C/T]AGTTTTCTGGTGGGG	10342
rs566930464	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100723885	GTTGACTGTAAGTCA[A/G]GTCTTCCAGAAAATC	10342
rs566931858	snp	A/C	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100738072	GAGACCCTGTCTCAA[A/C]AACAAACAAAGCCAA	10342
rs567124043	snp	A/C	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100713121	AGGTAAAAAGCAGGC[A/C]GACTGGTTAGGAGTC	10342
rs567204327	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	TFG	GRCh38.p7	3:100710299	CTGGACACTACAGTA[A/G]GTATTTTGGATGCAC	10342
rs567281839	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100719710	CTAATAAATATTAAG[A/G]CACTTAATGGATTCA	10342
rs567314451	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100746494	ACTCCATAAAAGGCT[A/G]GATGTCCTATGTATT	10342
rs567336770	snp	A/G	0.00279162	0.0372561	intron-variant	TFG	GRCh38.p7	3:100747990	TTTGATAACTACTTG[A/G]TCTTGAAATATTATG	10342
rs567370387	snp	A/G	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100732804	GGGTTCTGCTTAACA[A/G]ATTTTTACATATGTG	10342
rs567611065	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100726238	GGAGTGGAAGCAAGC[A/G]TCTGGCATAGGAGGG	10342
rs567701231	snp	A/C	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100730957	TAGGGAAGATAGATA[A/C]CTGGTAGACATGTTT	10342
rs567707459	snp	A/G	0.00755907	0.0610114	intron-variant	TFG	GRCh38.p7	3:100742178	TGACAGTCCCATTTG[A/G]ACTTGAATGAGGTGG	10342
rs567732668	snp	C/T	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100717998	GGTGTGATCATGGCT[C/T]ATTGAAGCCTTGAAC	10342
rs567739098	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100730279	ATGAGTTTTTTGCTT[C/T]AGGTGAAACTTTTTC	10342
rs567864320	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100723964	TTCTTTAGAGACTAT[C/T]GGACAGAATATGTAA	10342
rs567901297	snp	A/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100711372	TCCCAAAGTGCTGGG[A/T]TTACAGGTGTGAGCC	10342
rs567985984	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100737802	GCCTATAATCCCAGC[A/G]CTTTGGGAGGCCGAG	10342
rs568001372	snp	A/C	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100734309	TTGCTCTAGGTGCTG[A/C]ATTTTTCTCTGAGCC	10342
rs568292167	snp	A/T			intron-variant	TFG	GRCh38.p7	3:100714171	TATTGAATGTGATGT[A/T]CCTATAGTTACTATA	10342
rs568374347	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100715309	ATTGACATTGGCAAG[C/T]AGATGAGTGAAGACA	10342
rs568493891	snp	A/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100717541	TATAAGCATGGGATG[A/T]CATTACATATGTATG	10342
rs568574172	snp	G/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB, utr-variant-5-prime	TFG	GRCh38.p7	3:100709488	TTTTTTCTTGCTCCC[G/T]CCTCTGTTCTTCCCC	10342
rs568649046	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100718054	CTCAGCCTCCCGTGT[A/G]GCTGGGACTGCAGGC	10342
rs568713801	snp	A/T			upstream-variant-2KB	TFG	GRCh38.p7	3:100708463	TTTTTCTTTTATAAC[A/T]GGTAAACAACTGGAG	10342
rs568797625	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100714362	AAAAATTAGCTGGGC[A/G]TGGTGGTGTGCGCCT	10342
rs568815328	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100729439	AAGCAAAATGTGTCA[A/G]CATTTGGAACTGACA	10342
rs569098530	snp	A/C	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100737376	ATGAAATATAACCTG[A/C]AAGCTCCATATTTAA	10342
rs569191223	snp	C/G			intron-variant, upstream-variant-2KB	TFG	GRCh38.p7	3:100710756	GTCATTTCTGGACTT[C/G]AGAGGGGGCGGGGCA	10342
rs569196991	snp	C/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB, utr-variant-5-prime	TFG	GRCh38.p7	3:100710193	AATCGGAGCCTAGTT[C/T]CTTGGCTAAGTCAGC	10342
rs569330839	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100730159	TTCAGGGGATTTAAC[C/T]ATCTGCAGAATATTA	10342
rs569340136	snp	A/C/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100742514	GCAAAGTGGGGACCA[A/C/G]CCCTGACAGGTTGCT	10342
rs569451282	snp	C/T	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100729494	AAAATGTGGACTGAC[C/T]TTTAAGTATGTGTTA	10342
rs569486879	snp	A/G	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100715026	CTTGCAGTGTATTTA[A/G]TCTTGACCTCACTGT	10342
rs569542286	snp	C/T	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100735809	GTGCTAGGCCTTGTT[C/T]GGCAGACAAAAAGAA	10342
rs569609872	snp	A/C	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100715968	AAATAATAATTGTAC[A/C]TATTTATGGGGTACA	10342
rs569645200	in-del	-/A	0.00279162	0.0372561	intron-variant	TFG	GRCh38.p7	3:100739392	ATATTGAGCATCATT[-/A]AAAAAAAAACCAAAA	10342
rs569691478	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100720708	ACCCTTGCTTTAGAC[A/G]GTATTTCCCGAGGGG	10342
rs569693444	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100727925	CTGGACTTCCCCTCC[C/T]GGGATCAAGCAATCC	10342
rs569732194	snp	C/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100727370	AGTATGTGAATTACT[C/G]TGAGTTTTCTTCTAA	10342
rs569790011	snp	C/T	5.17112e-05	0.00508458	intron-variant	TFG	GRCh38.p7	3:100732477	TAGATAAAAAGGAAA[C/T]AAGTTTTTGTTTATT	10342
rs569855086	snp	C/T	0.00119737	0.0244387	intron-variant	TFG	GRCh38.p7	3:100721465	ATATTTTAGAAAAGT[C/T]TACCTTGATACAGGG	10342
rs569865754	in-del	-/ATT			intron-variant	TFG	GRCh38.p7	3:100729591	AAAACTCTTATTATT[-/ATT]TTTTTCTTTTTACAA	10342
rs570049394	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100734824	AGACTAGAATAATAT[C/T]AATATGATTCACATT	10342
rs570099094	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100737196	AAATTTAGCAATATG[C/T]CTTTAATGGAAAAAA	10342
rs570099131	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100729653	TTAAAACTGTCCATA[C/T]TGTGAAATAGTAATT	10342
rs570141541	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	TFG	GRCh38.p7	3:100707317	CTTTACTGATGGCTT[C/T]GGGATGAAGCATGAG	10342
rs570167142	in-del	-/TAAAG	0.00318978	0.0398085	utr-variant-3-prime, downstream-variant-500B	TFG, ABI3BP	GRCh38.p7	3:100748882	ATTAACATGATGTAC[-/TAAAG]TAAAGTAGAGCCCTT	10342
rs570259627	snp	G/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100730203	AGAATTTAACCAGTA[G/T]AGCCAATACTGTTCA	10342
rs570260388	snp	A/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100740124	AAACTTACATGTTTC[A/T]AAAATCCCTTACATG	10342
rs570278179	snp	A/T	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB	TFG	GRCh38.p7	3:100709401	GGACCCAGCCAGCCC[A/T]GCGCCTCGCGCCGTC	10342
rs570287832	in-del	-/T/TT	0.0581099	0.160244	intron-variant	TFG	GRCh38.p7	3:100743803	AGTTGATATAATGTC[-/T/TT]TTTTTTTTTTTCTCA	10342
rs570653415	snp	A/G	0.00159617	0.0282053	intron-variant	TFG	GRCh38.p7	3:100715184	GTAATGCCAGCAGAT[A/G]TAATAGAAATCTTAA	10342
rs570781818	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100713531	CATAAATATGGTAAC[A/G]TGGGGATAATGAATC	10342
rs570804056	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100722026	TGTAGTGGTGTGTGC[C/T]TGTAGTCCCAGCTAC	10342
rs570838774	snp	G/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100728629	TTTTTTAAAGGAATT[G/T]TATTTATTTTTCCTT	10342
rs570908899	in-del	-/ATAG	0.00279162	0.0372561	intron-variant	TFG	GRCh38.p7	3:100729216	ACCCTTTTTAGTATA[-/ATAG]ATAAGTAATGAACCT	10342
rs570933424	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100731092	TGCTGTGGGTACTTA[C/T]ATTCGGTTTAGCACT	10342
rs571009450	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100728166	ACGATTTCTTTTAAG[A/G]TCAGCTATTTTAGTT	10342
rs571047034	snp	C/T	0.00159617	0.0282053	intron-variant	TFG	GRCh38.p7	3:100734927	ACTTTTGTAGTTCTT[C/T]AGGTGTGATGTGGTA	10342
rs571137638	snp	C/T			intron-variant, utr-variant-5-prime, upstream-variant-2KB	TFG	GRCh38.p7	3:100709720	GCGGCCTCCGCAAGC[C/T]GGTATGGCCACTGGA	10342
rs571154470	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime	TFG	GRCh38.p7	3:100748636	AGAAATTTAAAAGCA[C/G]AGCATTTTTTATGAT	10342
rs571283315	snp	A/C	0.000798403	0.0199641	downstream-variant-500B, utr-variant-3-prime	TFG, ABI3BP	GRCh38.p7	3:100749346	AATCTTAAAAAAAAA[A/C]TACATCTCTTTATTG	10342
rs571298392	snp	C/T	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100739957	CTCAACAGTGATTCT[C/T]AATGTCAACGTGTGC	10342
rs571325711	snp	A/C	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100740899	TCAACAGTGGACTGC[A/C]TATATGATGGTGGTC	10342
rs571333036	snp	A/G	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100739460	TGTTACAGGAAGACT[A/G]TGTGATGTTGCCAGA	10342
rs571508088	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100711397	TGAGCCACCGTGCCC[A/G]GCCCTCAAATTTTAA	10342
rs571508198	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100718708	AATTATAGGCACACA[C/T]CACCACACTCGGCTG	10342
rs571830968	snp	A/G	0.00755907	0.0610114	intron-variant	TFG	GRCh38.p7	3:100721980	ACACGGTAAAACCCT[A/G]TCTCTACTGAAATGC	10342
rs571851419	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100712187	ATTAATTTAAGGACT[A/G]GTTAGATGGAAGGAC	10342
rs572039756	snp	C/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100741012	GTGTTTGTGGTGATT[C/G]TGGTGTAAACAGACT	10342
rs572085156	in-del	-/TTTA	0.00517822	0.0506191	intron-variant	TFG	GRCh38.p7	3:100747683	GTGAAAATGGTACTT[-/TTTA]TTTATTTGCAAAATT	10342
rs572101227	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100727356	ATAGCTATGCAGGGA[A/G]TATGTGAATTACTGT	10342
rs572126486	snp	A/G	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100725810	AAAAAATATAAATAC[A/G]TATTAAGCTTTAACA	10342
rs572128937	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100727512	TATGTATACTGGCAA[C/T]GTGCAAAGCATTTTA	10342
rs572213238	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100713310	GATTTTTTTGTCTTA[C/T]ACAACTCGAAGGAAG	10342
rs572241531	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	TFG	GRCh38.p7	3:100707368	CCTCAAGTTGCTTTC[A/G]GAGTCCATGAGCTCC	10342
rs572300331	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100732389	GTAATCCTATATTCC[A/G]ACATGCTTAACATTC	10342
rs572336017	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100719198	CATCCCAGAAGTAGT[C/T]TTGTGGCCTCCCCAG	10342
rs572477047	snp	C/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100711502	TTTTTTCTTAATTAG[C/G]AGTGTGTCTGATGGA	10342
rs572486636	snp	G/T	0.00398564	0.0444627	intron-variant, upstream-variant-2KB	TFG	GRCh38.p7	3:100710923	CCTTGAAGGGAAAGT[G/T]TTGTTGCACACTTAC	10342
rs572495446	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100712639	AATGACTGTTGTCTG[C/T]TAGGCACTGTTGTAG	10342
rs572514786	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100718067	GTAGCTGGGACTGCA[A/G]GCATGTGCCACTGCA	10342
rs572514904	snp	C/G	0.00795532	0.062565	intron-variant	TFG	GRCh38.p7	3:100711101	AAAGTATACGTGACT[C/G]AATTTTTTTTTTTTT	10342
rs572585416	snp	G/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100739205	TTACCAACATAAAAT[G/T]TATTACTTATAATTT	10342
rs572595977	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100739528	AGAGATCGGGAGATA[C/T]TGCTGTTTGACAGCC	10342
rs573056303	snp	G/T			intron-variant	TFG	GRCh38.p7	3:100737271	CCTTGGATATGCAGT[G/T]TAGTCTCTCTGGGTT	10342
rs573190955	snp	A/G	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100744454	GGACTTAGATGATAT[A/G]AATGGTATTTGTCCC	10342
rs573273361	snp	A/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100737477	CTGCAGAATGTGACT[A/T]AGTACTTAACTAATC	10342
rs573306366	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100736948	ATGAATATAGATACA[A/G]AGTGAAAGACCAGTC	10342
rs573444372	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, upstream-variant-2KB	TFG	GRCh38.p7	3:100709644	CCGCCTCCCCGCGAC[A/G]CCCCAGTCCAGTGGC	10342
rs573454673	snp	C/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100743700	CTTAGACACGTATAG[C/G]GCTGAGCAGCTGGTA	10342
rs573482633	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	TFG	GRCh38.p7	3:100709271	GGAAATACCCGCTTT[A/C]GAGAAAACCGGAAGT	10342
rs573484602	snp	C/T	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100716028	TAGATCAGGGTAATT[C/T]GCATATCCATCACCT	10342
rs573620695	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100739689	CTTCAACACTTACCA[A/G]TATTTTGGCATTCTT	10342
rs573755850	snp	C/G	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100711189	CTCACTGCAACCTCC[C/G]CCTCCCGGGTTCAAG	10342
rs573783786	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100747003	AAAGATACTTGATTT[A/G]CTTATTAAGAACTAA	10342
rs573836171	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100720892	GTGAAAAATAAAATG[C/T]GTACACTTTTTCCGG	10342
rs573892114	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100711633	AAAGTCTTTAAATTC[C/T]ATATGTCAGGCACTT	10342
rs573936916	snp	A/T	0.00517822	0.0506191	intron-variant	TFG	GRCh38.p7	3:100741513	AAAGTATTAAAAAAG[A/T]TAAAAAATCAAGTTT	10342
rs573951607	snp	A/C			intron-variant	TFG	GRCh38.p7	3:100735296	TGGTAAGTTCTGGGG[A/C]TACATCAGAGCAGAA	10342
rs573963306	snp	C/T	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100745198	TTAATACAAAGCTGT[C/T]TTACTAACATTATCA	10342
rs573982536	snp	A/T	0.00159617	0.0282053	intron-variant	TFG	GRCh38.p7	3:100738222	TCAACCAACTTTAAT[A/T]AACTCCTCCTCTGCA	10342
rs574116853	snp	A/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100723292	ACATGTAAGAGTTAT[A/T]ATTGAAAAATTAGAC	10342
rs574134215	snp	G/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100724286	CAATTTTGAAAAGAT[G/T]CAGTTGGCAAATCTT	10342
rs574136922	snp	G/T			intron-variant	TFG	GRCh38.p7	3:100717031	TGCTGTGCAGAAAAG[G/T]TTTCCAGTTTGAGAT	10342
rs574278341	snp	C/T	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100744545	CTTATCTGTTGGCAG[C/T]TGGGTTGGAAAACAT	10342
rs574283910	snp	C/G	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100729092	CCTACTGGAGCGTAG[C/G]ACCTGGAAATCCCAT	10342
rs574440601	snp	C/G			intron-variant, utr-variant-5-prime, upstream-variant-2KB	TFG	GRCh38.p7	3:100709601	GAGGTGCGGCGGTCG[C/G]GAAGGGCAACCGAGG	10342
rs574501125	snp	A/G	0.0023933	0.0345097	upstream-variant-2KB	TFG	GRCh38.p7	3:100708561	GTTTGGCCAAACTTC[A/G]GGCTCCTGGGCCTTC	10342
rs574524440	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, upstream-variant-2KB	TFG	GRCh38.p7	3:100709821	CCGCGCGGCAGCTGG[C/G]GTCGGAGGCACTGTG	10342
rs574645040	in-del	-/TAACTAACTA/TAACTAACTT	0.00557933	0.0525774	downstream-variant-500B	TFG, ABI3BP	GRCh38.p7	3:100749071	GAAGTATAAACATTT[-/TAACTAACTA/TAACTAACTT]TAACTAACTTACAGA	10342
rs574911490	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100716822	TTTTTTCATATATTT[A/G]TTGACCATTTCTATG	10342
rs574962439	snp	A/G	0.0023933	0.0345097	intron-variant	TFG	GRCh38.p7	3:100721685	AGGGGTATATTCTCA[A/G]TCCAGGTCACATAGG	10342
rs574967168	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100744614	TTGCACTTAATGTTT[A/G]TTGCCAGTTAGTTCT	10342
rs575087670	snp	G/T	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100723347	AAAACAAGGGTACCT[G/T]TTCAGTTCAGTAGAA	10342
rs575106192	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100728208	TTCAAGACAAAGTTA[C/T]GCAAGAGGGATAACA	10342
rs575151410	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100723673	TAGGACTATATAGCA[A/G]TCTGAACACTTATGC	10342
rs575199509	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100711589	ATCTATATTACAGCT[C/T]TCTTCTCCCATAATT	10342
rs575201546	snp	A/C			intron-variant	TFG	GRCh38.p7	3:100712327	GGTGAGTGCTTTCAC[A/C]TACCCCGAAAGAATA	10342
rs575314937	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100735984	CAAGAAGGCTTACTA[A/G]AAGTGTGGAATTATA	10342
rs575334936	snp	C/T	0.00159617	0.0282053	intron-variant	TFG	GRCh38.p7	3:100730407	AAAATTGGTTTCTTC[C/T]CTGCATTTTGGAAAT	10342
rs575407088	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100733357	TCGCTGTGATTTCTA[A/G]TATGCTGTGGAACCT	10342
rs575607488	in-del	-/AAG	0.0134861	0.0810011	intron-variant	TFG	GRCh38.p7	3:100730663	TGGCTTACCCTCACC[-/AAG]AAATGTGGCCACCTG	10342
rs575658967	snp	C/G	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100736883	AGAACAATATGTCAG[C/G]TATGTTTCCAATTAT	10342
rs575746716	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100742806	GTGTAAAAGGAATCT[C/T]GTGTAGAGATATAAT	10342
rs575881992	snp	C/G	0.0217236	0.101931	intron-variant, upstream-variant-2KB	TFG	GRCh38.p7	3:100709838	TCGGAGGCACTGTGG[C/G]AAGGGGCTGGAGGGA	10342
rs575896933	snp	C/T	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100741893	GACTGCTATGTACCA[C/T]ATAGCCTAGCTATGT	10342
rs575924374	snp	A/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100714894	TTTCGGCAAACACAC[A/T]GAGTAGAATTATAGT	10342
rs575962978	snp	G/T			intron-variant	TFG	GRCh38.p7	3:100737591	AACAAACACCAGGTG[G/T]TGCTCTAACTATTTG	10342
rs576014877	snp	A/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100735195	ATTTTGGCAATCATC[A/T]GTCTCTCTTGCATTA	10342
rs576145051	snp	A/G	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100714226	TAAGTGGGGCCGGGC[A/G]CAGCAGCTCATGCCT	10342
rs576162644	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100721718	TCTCACAGACAAAAC[C/T]GTAAGACACATGAAG	10342
rs576220463	snp	A/G	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100734458	TCCTCCTAAATCTTC[A/G]GCTGCTTGTCTAGCC	10342
rs576424089	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100725231	TCTTTTACCTCATAT[A/G]GGGGCATTTATTACG	10342
rs576572803	snp	G/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100733727	GTAGTGACTTGGACT[G/T]ATATTCTTTTGAGGA	10342
rs576843480	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100714108	TGCCCATTTTTATTG[A/G]ACTCTTTCCCATCCT	10342
rs576910438	snp	A/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100723240	ACCTTTAGATTTTTT[A/T]AATTGCATACTACAT	10342
rs577028897	snp	A/C			upstream-variant-2KB	TFG	GRCh38.p7	3:100708249	GTGTTCAAATAAGGC[A/C]AACGCCAACCTGTAA	10342
rs577276141	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, downstream-variant-500B	TFG, ABI3BP	GRCh38.p7	3:100748937	AAATGTAACACTGAT[A/G]ATAGGTTAATAAAGA	10342
rs577351174	snp	G/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100720373	TAAATTGTAATTATC[G/T]TCCTTCACATTACAG	10342
rs577352514	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100727454	GAACTTTTATTTTCA[C/T]GTAGATGTCCTTTTC	10342
rs577370105	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100722993	AAAGCTTTTCCATTG[A/G]TACAGAAAAAGTCAA	10342
rs577389897	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100726751	AGAACAATAGGATGT[C/T]TTACAAGTATGTTAG	10342
rs577420420	snp	G/T	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100720750	TAAAAATAGTTCTGA[G/T]AAAAACCAATAGAAG	10342
rs577569924	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	TFG	GRCh38.p7	3:100707318	TTTACTGATGGCTTC[A/G]GGATGAAGCATGAGG	10342
rs577602832	snp	C/T	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100748076	TTTTGGTCCACCTAA[C/T]AGTAAGACTAATTCT	10342
rs577711433	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100740182	TTTATTACTGTGTAA[C/T]TATTATCCCAAAACA	10342
rs577746953	snp	C/G	0.00199481	0.0315187	intron-variant	TFG	GRCh38.p7	3:100738355	ATCAAGCGAACTAAA[C/G]ATTTGTTTTTAAATA	10342
rs577750619	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100739786	CAGCTTATTATACTC[A/G]GGTATTTCAGTATAT	10342
rs577891444	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100714383	GTGTGCGCCTGTAAT[C/T]CCAACTACTCGGGAG	10342
rs577916591	snp	A/C	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100745935	CTATTTACTATCTGG[A/C]TCTTTACAGAAAAGT	10342
rs577918435	snp	C/G	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100738325	GTATAGGTATGATGA[C/G]AGTTTAATGCCTACA	10342
rs577929149	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100719111	AGCTAAAAACAGTTA[C/T]AAAATTCTCAGTTTT	10342
rs577948114	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100725033	CTCAGCTTCCCGAGT[A/G]GCTGGGACTACAGGC	10342
rs577992349	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100724450	GTATCCTAGGTAAAT[C/T]TAATGTACTGTTTCA	10342
rs578009544	snp	C/T	0.000798403	0.0199641	intron-variant	TFG	GRCh38.p7	3:100725544	AGCACTTTGGGAGGC[C/T]GAAGTGGGCAGATCA	10342
rs578077016	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100738056	GCCTGGGCAACAGAA[C/T]GAGACCCTGTCTCAA	10342
rs578110879	snp	A/G	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100718411	CATCTTTTTTTTACA[A/G]TGTAAAAACCATTTT	10342
rs578170566	snp	C/T	0.000399281	0.0141238	intron-variant	TFG	GRCh38.p7	3:100731338	GTTAAAATTCTTGAA[C/T]TCTTTTTCTTTCACA	10342
rs578255104	snp	C/T			intron-variant, upstream-variant-2KB	TFG	GRCh38.p7	3:100710328	ACTGTCTCATTTAAT[C/T]ATCACAAGGATTCCT	10342
rs587777175	snp	C/T	9.89707e-05	0.00703389	TFG	3	allele_origin=T(germline)/C(germline)	3:100728759	CAGGTGAAATATCTC[C/T]GTCGAGAACTGATAG	10342
rs587777789	snp	G/T			missense	TFG	GRCh38.p7	3:100744917	AGCCTCAACAGTATG[G/T]TATTCAGTATTCAGG	10342
rs745351773	snp	A/G			upstream-variant-2KB	TFG	GRCh38.p7	3:100707438	CTCTCTTCCTAGCGT[A/G]CAGATGACCACAGTG	10342
rs745437158	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100740523	TATTTTCTTGGTATA[C/T]AGGTCAGCCCTATTC	10342
rs745447595	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100737786	AGGTGTGGTGCCTCA[C/T]GCCTATAATCCCAGC	10342
rs745478256	snp	C/G	1.6489e-05	0.00287128	missense	TFG	GRCh38.p7	3:100713738	TCAAAGCTCAACTTG[C/G]GGAGGATATTCGGCG	10342
rs745496440	snp	C/T	1.72734e-05	0.00293878	intron-variant	TFG	GRCh38.p7	3:100748141	TGTTATTTATTTTGC[C/T]TTTTCAGCAAGCTAT	10342
rs745520197	snp	A/C			intron-variant	TFG	GRCh38.p7	3:100729338	AATGGTATGTTGTAA[A/C]TTTGAAACACAGTTT	10342
rs745536459	snp	A/T	0.000190301	0.00975266	intron-variant	TFG	GRCh38.p7	3:100713896	TTTAAAGCTATTTTT[A/T]AAAGTCTTTTTAAAA	10342
rs745554610	in-del	-/T			intron-variant	TFG	GRCh38.p7	3:100743661	CATAGTTGTATCTCC[-/T]TTAGTGCTACCCAGC	10342
rs745627731	snp	A/T			intron-variant	TFG	GRCh38.p7	3:100713296	GAGAGATCAACCAAG[A/T]TTTTTTTGTCTTATA	10342
rs745681029	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100711992	ATTGTGAGAACTGGC[A/G]GATAAAAAGCTAACT	10342
rs745681175	in-del	-/G			intron-variant	TFG	GRCh38.p7	3:100736765	TACATGTGTAGAAGT[-/G]GTTTATTACAGCATT	10342
rs745741115	snp	C/T	1.65081e-05	0.00287293	synonymous-codon	TFG	GRCh38.p7	3:100732539	GGAAGAAAAGTCTGC[C/T]TCTGATTCTTCTGGA	10342
rs745767046	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100719278	CCCTGATGAACTCCT[C/T]GTCTCTGGCTGCTTT	10342
rs745801389	snp	C/T	1.6577e-05	0.00287893	missense	TFG	GRCh38.p7	3:100732643	AAAATGTTATGTCAG[C/T]GTTTGGCTTAACAGA	10342
rs745833586	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100742285	CGTATGAGGAAATCA[A/G]TTCTACCATAGGCTA	10342
rs745847259	in-del	-/AAGAT	1.80237e-05	0.00300192	intron-variant	TFG	GRCh38.p7	3:100748113	AAGTAGTTTTACTAA[-/AAGAT]AAGATACATGTTATT	10342
rs745926478	snp	C/G			upstream-variant-2KB	TFG	GRCh38.p7	3:100709263	CGAGAAACGGAAATA[C/G]CCGCTTTCGAGAAAA	10342
rs745985607	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100713317	TTGTCTTATACAACT[C/T]GAAGGAAGATAAAGA	10342
rs746044234	snp	C/T	4.9543e-05	0.00497685	synonymous-codon	TFG	GRCh38.p7	3:100748468	AAGTGGGCCTAATCC[C/T]TATGCGCGTAACCGT	10342
rs746086227	snp	A/G	3.30077e-05	0.00406236	synonymous-codon	TFG	GRCh38.p7	3:100728746	CCTTGAATCAAGTCA[A/G]GTGAAATATCTCCGT	10342
rs746097471	snp	A/G	1.72832e-05	0.00293961	utr-variant-3-prime	TFG	GRCh38.p7	3:100748535	GGTTATCGATAAGGA[A/G]GCTCCTCTACACCAA	10342
rs746154931	snp	C/T			intron-variant, upstream-variant-2KB	TFG	GRCh38.p7	3:100710409	TGGAGGACTTAAGAT[C/T]ACATAGCTAGTAGTG	10342
rs746234370	snp	C/G	1.64955e-05	0.00287184	missense	TFG	GRCh38.p7	3:100728816	TTGGATAGCTTGGAA[C/G]CACCTGGAGAACCAG	10342
rs746429597	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100717156	TGAGTGGTCTTGTCA[A/G]AAGTCAGTTGGCTAT	10342
rs746447288	in-del	-/T			intron-variant	TFG	GRCh38.p7	3:100737054	AGATGCTATTTTATC[-/T]CCCTCCTTTCTTCAA	10342
rs746506910	snp	A/C			intron-variant	TFG	GRCh38.p7	3:100725131	CAGGATGGTCTCGAT[A/C]TCCTGACCTTGTGAT	10342
rs746596847	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100726516	AATTTAAACTTAGCT[A/G]ATTTAAACTTTTAAT	10342
rs746654375	in-del	-/T			intron-variant	TFG	GRCh38.p7	3:100715891	ATTCAGATTTTTAAC[-/T]TTTTTTTTTTTTTAG	10342
rs746679944	snp	A/C/T	3.47254e-05	0.00416674	utr-variant-5-prime	TFG	GRCh38.p7	3:100713650	TTTATCAGTCTTTCT[A/C/T]TAGAGTTGTATATAT	10342
rs746691912	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100724648	GAAAACCAGCCAAGG[A/G]AAATGCAAACCAGTG	10342
rs746764716	snp	A/G	3.30115e-05	0.00406259	missense	TFG	GRCh38.p7	3:100713728	AAGCTAATCATCAAA[A/G]CTCAACTTGGGGAGG	10342
rs746792001	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100746257	ATGCTTTAGAATCAC[C/T]TGGGGGAGGCTATGT	10342
rs746801392	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100714458	TGAGCCAAGATCGTG[C/T]CACTGCACTCCAGCC	10342
rs746873285	snp	A/G	1.65386e-05	0.00287559	utr-variant-3-prime	TFG	GRCh38.p7	3:100748583	TATTGGCCTCCCAAA[A/G]GACTCCAGTACTATT	10342
rs746903056	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100740276	TTAGCTGGGTGATTT[C/T]GGCTCAGCATCTCTC	10342
rs747127184	in-del	-/C			intron-variant	TFG	GRCh38.p7	3:100734434	GTAGCACCTTCACTT[-/C]CGGGATTTTCCTCCT	10342
rs747140985	snp	A/T			intron-variant	TFG	GRCh38.p7	3:100729670	GTGAAATAGTAATTT[A/T]AAAAAAGTCTAGACT	10342
rs747158824	snp	C/G			intron-variant	TFG	GRCh38.p7	3:100740482	TTTATAGCCTGTCCT[C/G]AGAAATGTCACTGTC	10342
rs747193334	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100742988	ACTCATTGATGACCA[C/T]AGTCTACTACTACGT	10342
rs747261358	snp	C/T	6.61233e-05	0.00574955	missense	TFG	GRCh38.p7	3:100748298	TACCAGGCGAGCAAT[C/T]ATCCTGCACAAACTT	10342
rs747309093	in-del	-/TAC			upstream-variant-2KB	TFG	GRCh38.p7	3:100709140	TTCTTTTTCAGCTGT[-/TAC]TACAATGGTCAACAA	10342
rs747351961	snp	G/T			intron-variant	TFG	GRCh38.p7	3:100718386	TGTGGGTCACATAAG[G/T]CCTCTGTCTCATCTT	10342
rs747353898	snp	C/G	3.30879e-05	0.00406729	synonymous-codon	TFG	GRCh38.p7	3:100720015	TAGTTCTGACCTTTC[C/G]TTTGCAATTCAGTGC	10342
rs747373198	snp	C/T	1.6486e-05	0.00287102	missense	TFG	GRCh38.p7	3:100748437	CACTTCCTGGAAGTA[C/T]CATGACCCCTCCTCC	10342
rs747459358	snp	G/T			intron-variant	TFG	GRCh38.p7	3:100736357	TCAGGAATATAGTAC[G/T]CTACACTTTATAAGG	10342
rs747476366	snp	A/T	3.38301e-05	0.00411265	intron-variant	TFG	GRCh38.p7	3:100728703	AGCAAATAAATGTTT[A/T]TATTTCAGTTAATGG	10342
rs747477300	snp	A/C			intron-variant	TFG	GRCh38.p7	3:100747489	TAAAAGTTTTCAGTG[A/C]AGCAGACTTTCGTTG	10342
rs747589738	snp	A/G			missense	TFG	GRCh38.p7	3:100748254	TTTCTGGTCAGCCTC[A/G]ACAACTGCCTGCTCA	10342
rs747646332	snp	C/G	1.76372e-05	0.00296956	intron-variant	TFG	GRCh38.p7	3:100728664	CATATTATTAGTATA[C/G]TTATTCATGAACTTC	10342
rs747685403	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100727101	ATGGACTGTTGATCT[A/G]TCACAGATTATAGTC	10342
rs747750136	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100747032	AAGCTTGCTCTTAAT[A/G]AATTTAGTCAGGGTC	10342
rs747842186	snp	C/T	1.65141e-05	0.00287346	missense	TFG	GRCh38.p7	3:100736582	ACTATCCAGGGCCAC[C/T]CAGTGCTCCTGCAGA	10342
rs747882164	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100722029	AGTGGTGTGTGCCTG[C/T]AGTCCCAGCTACTTG	10342
rs747882521	snp	C/T	1.64866e-05	0.00287106	missense	TFG	GRCh38.p7	3:100736677	CAGCCACAGCAGCCA[C/T]CATATACAGGAGCTC	10342
rs747995643	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100747729	TTAGTACAATAAGAT[A/G]TATTTATAGTATTAT	10342
rs748038848	in-del	-/TT	0.00203709	0.0318496	intron-variant	TFG	GRCh38.p7	3:100713910	TAAAGTCTTTTTAAA[-/TT]AAAAAAAAAAAAAAG	10342
rs748160989	snp	C/G			intron-variant	TFG	GRCh38.p7	3:100730815	GAGCAAGTAGTAGGA[C/G]GTATAGTATGTTTCC	10342
rs748248786	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100718445	TTCACAGACCTATAA[C/T]AACACAGGGATTTTG	10342
rs748305210	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100732098	TAGTTCAGTTTCTTT[C/T]TATAAAATAAAGCCT	10342
rs748541515	snp	A/C			upstream-variant-2KB	TFG	GRCh38.p7	3:100707766	ATTCAGTTTTAAAAA[A/C]TAAGCAATGAATAAC	10342
rs748541751	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100738128	TGTTGGATGAACACC[A/G]GTCATTATGGACTAG	10342
rs748545117	snp	A/T			intron-variant	TFG	GRCh38.p7	3:100739244	AGCAATCTCTTACAA[A/T]GTGTTAATAGTCCAT	10342
rs748570723	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100719177	GTTAAAGTAGGTGCA[A/G]CAGAGCATCCCAGAA	10342
rs748573409	in-del	-/G			intron-variant, upstream-variant-2KB	TFG	GRCh38.p7	3:100710550	CTCCCCTCAGGAGGT[-/G]CTTAAGCCACAGCCT	10342
rs748670012	snp	A/G	1.66131e-05	0.00288206	missense	TFG	GRCh38.p7	3:100719977	TTTTAAATTCCAGAT[A/G]GAGATCTTATAACAA	10342
rs748748401	in-del	-/A			intron-variant	TFG	GRCh38.p7	3:100718230	GTGTGCCTGGCCTTT[-/A]ACTGCCTTTTTTCCC	10342
rs748798297	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100746534	ACTCACATAATTTCC[A/G]TATTTCCATTTTTTT	10342
rs748815070	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100719666	CCAACAATTTATGAT[A/G]TTGCTCTCTATGAAT	10342
rs748826156	snp	A/G			missense	TFG	GRCh38.p7	3:100748188	CTCAACAACCTCAGC[A/G]GTTCCAGGGATATGG	10342
rs748871102	snp	C/T	1.68912e-05	0.00290608	intron-variant	TFG	GRCh38.p7	3:100719958	AAAAAACAACCTTTT[C/T]TTTTTTTAAATTCCA	10342
rs748874477	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100744973	CTCATGGTTTTTTGT[C/T]TCTATACTCATTAAA	10342
rs749019066	snp	A/G			intron-variant, upstream-variant-2KB	TFG	GRCh38.p7	3:100710786	AAGGACAAGATGGGA[A/G]AAGAGCTTGTCGTAG	10342
rs749070427	snp	A/T			intron-variant	TFG	GRCh38.p7	3:100735725	CATTGGAACTGTAAT[A/T]TATTCTCTCCATTCA	10342
rs749073068	snp	A/G	1.66657e-05	0.00288662	missense	TFG	GRCh38.p7	3:100732658	CGTTTGGCTTAACAG[A/G]TGATCAGGTTTCAGG	10342
rs749129135	snp	A/C			intron-variant	TFG	GRCh38.p7	3:100723329	AGGAAAGGAGAAAAA[A/C]AGAAAACAAGGGTAC	10342
rs749145428	in-del	-/A	1.91203e-05	0.00309189	intron-variant	TFG	GRCh38.p7	3:100719943	AAAATTTAAAAAATT[-/A]AAAAACAACCTTTTT	10342
rs749175014	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100741994	TACTCTTGTCATTAA[A/G]CAATGCATGACCATA	10342
rs749200284	snp	A/G	1.65891e-05	0.00287998	intron-variant	TFG	GRCh38.p7	3:100736566	AACTGACTTTTTTTT[A/G]ACTATCCAGGGCCAC	10342
rs749401466	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100732411	TTAACATTCCAGACT[A/G]TCATTATACACCTGC	10342
rs749474872	snp	C/T	1.65531e-05	0.00287686	missense	TFG	GRCh38.p7	3:100728841	AACCAGGACCTTCCA[C/T]CAATATTCCTGAAAA	10342
rs749541589	snp	A/G			upstream-variant-2KB	TFG	GRCh38.p7	3:100708622	AACTCAGTTTCAGCA[A/G]AGAACCTTGTTAAGG	10342
rs749557696	in-del	-/TTTT			intron-variant	TFG	GRCh38.p7	3:100718551	TTTGTATTTCATGGT[-/TTTT]TTTTTTTTTTTTTTT	10342
rs749579157	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100721516	CTTATACCTTGGGCC[A/G]TCAGGGGCTTGGGAA	10342
rs749654396	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100727242	CCAGACCAGTTTCTG[A/G]CTGCTAGGAGCTGTT	10342
rs749678709	snp	C/G			upstream-variant-2KB	TFG	GRCh38.p7	3:100709225	AAAAAGTTTAGAACA[C/G]CGCACTACGCCCCGC	10342
rs749758617	snp	A/G	1.64887e-05	0.00287125	synonymous-codon	TFG	GRCh38.p7	3:100744909	ACCTCAGCAGCCTCA[A/G]CAGTATGGTATTCAG	10342
rs749921268	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100718902	CCGTTAGATTCTGTT[A/G]GTAGAGTGGAGGGAT	10342
rs749972236	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100731701	AGCTGGGATTACAGG[C/T]ATGCATCACTGTGCC	10342
rs750061557	snp	G/T	1.66482e-05	0.0028851	synonymous-codon	TFG	GRCh38.p7	3:100748243	AGCTCCTGCCTTTTC[G/T]GGTCAGCCTCAACAA	10342
rs750194417	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100739627	GCCTTTATTATGTAA[A/G]TATTGAAACATACAT	10342
rs750204762	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100723793	AGCAGGCTCAAACAG[C/T]GTTGGTCTTGTACAT	10342
rs750217275	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100719951	AAAAATTAAAAAACA[A/G]CCTTTTTTTTTTTTA	10342
rs750232252	snp	C/G	1.64939e-05	0.0028717	missense	TFG	GRCh38.p7	3:100748355	AATTATACTGTGGCT[C/G]CTGCCTCTCAACCTG	10342
rs750270027	snp	A/T	1.66123e-05	0.00288199	intron-variant	TFG	GRCh38.p7	3:100720077	AGTAGTAAACTTTCT[A/T]ATGAATTTACTATTT	10342
rs750288276	snp	G/T			intron-variant	TFG	GRCh38.p7	3:100744560	CTGGGTTGGAAAACA[G/T]TTGTTTTTCTAGACT	10342
rs750392468	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100727728	ACAACTAGAGATTAC[C/T]GAGTAATCTCTGGCA	10342
rs750452438	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100714385	GTGCGCCTGTAATCC[C/T]AACTACTCGGGAGGA	10342
rs750463614	in-del	-/C			intron-variant	TFG	GRCh38.p7	3:100716813	TTTTGAGCATTTTTT[-/C]ATATATTTATTGACC	10342
rs750497893	snp	C/G/T			intron-variant	TFG	GRCh38.p7	3:100734740	TCATGGAATTACTCA[C/G/T]AAAAGAGAATTGTGT	10342
rs750499084	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100741387	TGTCATAATTTTTTT[C/T]TAAATGTTTAAAAAA	10342
rs750529550	in-del	-/ATTA			intron-variant	TFG	GRCh38.p7	3:100720930	GTTGTTTTGTTTAGC[-/ATTA]ATTTTATTTTTTTTT	10342
rs750558914	snp	A/G			downstream-variant-500B	TFG, ABI3BP	GRCh38.p7	3:100749105	CCATTCAGAGAAAAC[A/G]GTGCCATTTGGTTTT	10342
rs750581270	snp	C/T	3.37986e-05	0.00411074	utr-variant-5-prime	TFG	GRCh38.p7	3:100713684	ACATCCTGGAGTCCA[C/T]CATGAACGGACAGTT	10342
rs750723468	snp	G/T			intron-variant	TFG	GRCh38.p7	3:100723692	GAACACTTATGCATG[G/T]TAGCTTTAGATGTTT	10342
rs750736240	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100742818	TCTTGTGTAGAGATA[C/T]AATAAACCTCTGAAA	10342
rs750743499	snp	A/T			intron-variant	TFG	GRCh38.p7	3:100712520	AGGAGGAAGGAGTTA[A/T]GCTTGGAAAATGTTC	10342
rs750759898	in-del	-/CTT	1.65089e-05	0.00287301	cds-indel	TFG	GRCh38.p7	3:100732538	GGGAAGAAAAGTCTG[-/CTT]CTGATTCTTCTGGAA	10342
rs750797278	snp	C/T	1.73369e-05	0.00294417	intron-variant	TFG	GRCh38.p7	3:100732460	TTAGGCCTTACTGAA[C/T]ATAGATAAAAAGGAA	10342
rs750890272	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100730520	AATAATACAATCTGC[A/G]TTATATTTTTAGAGA	10342
rs750964585	snp	A/G	1.64972e-05	0.00287199	missense	TFG	GRCh38.p7	3:100732575	GTCTACTCAGGTTAT[A/G]GCAGCAAGTATGTCT	10342
rs750970124	in-del	-/G			intron-variant	TFG	GRCh38.p7	3:100746274	GGGGAGGCTATGTGT[-/G]GGGGCCCCATTCCCA	10342
rs751048857	in-del	-/AAA			intron-variant	TFG	GRCh38.p7	3:100713908	TTTTAAAGTCTTTTT[-/AAA]AAAAAAAAAAAAAAG	10342
rs751144573	snp	C/G			intron-variant	TFG	GRCh38.p7	3:100739818	TGTCCAACTGATAAT[C/G]TTCTTTTTAATATAA	10342
rs751225466	in-del	-/A	1.66468e-05	0.00288498	intron-variant	TFG	GRCh38.p7	3:100736555	TTGGATACTAAACTG[-/A]ACTTTTTTTTGACTA	10342
rs751322076	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100729056	GGTTTCATTATACCA[A/G]TTTCTGGATCTCATC	10342
rs751335113	snp	A/T			intron-variant	TFG	GRCh38.p7	3:100715341	AGTATGAAGAATCAT[A/T]TGGGAGATTTTACTC	10342
rs751338510	snp	C/T	1.78471e-05	0.00298718	intron-variant	TFG	GRCh38.p7	3:100748124	CTAAAAGATAAGATA[C/T]ATGTTATTTATTTTG	10342
rs751393611	snp	A/C/G	4.98304e-05	0.00499131	missense, synonymous-codon	TFG	GRCh38.p7	3:100748210	GGGATATGGCCAGCA[A/C/G]CCAACTTCCCAGGCA	10342
rs751406877	snp	A/G	0.000114416	0.00756275	intron-variant	TFG	GRCh38.p7	3:100713887	AAGAGTGTTTTTAAA[A/G]CTATTTTTTAAAGTC	10342
rs751516464	snp	A/T	0.000106366	0.00729189	intron-variant	TFG	GRCh38.p7	3:100719935	CAAATCTGAAAATTT[A/T]AAAAATTAAAAAACA	10342
rs751630061	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100724873	ATTCATATCTCAATC[A/G]TGTTGAAAAGTCGTA	10342
rs751673654	snp	C/G	3.34806e-05	0.00409136	intron-variant	TFG	GRCh38.p7	3:100736532	AGCTTGCTGGGGGAA[C/G]GCCTTGTGTTGGATA	10342
rs751676150	snp	A/C			intron-variant	TFG	GRCh38.p7	3:100736191	GGACCCTTAATGCCA[A/C]ACTAGGAGGTTGAAC	10342
rs751712852	snp	G/T			intron-variant	TFG	GRCh38.p7	3:100737219	GGAAAAAAAGCAGTG[G/T]ATTTTAAGTCAGACT	10342
rs751806481	snp	A/T	1.70702e-05	0.00292144	utr-variant-5-prime	TFG	GRCh38.p7	3:100713675	ATATATAGAACATCC[A/T]GGAGTCCACCATGAA	10342
rs751847082	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100731792	ACCTCAAGTGATCTA[C/T]CCACCTCGGCCTCTC	10342
rs751857236	snp	A/G	6.59848e-05	0.00574352	intron-variant	TFG	GRCh38.p7	3:100744817	TTTCCTTGTGTGTGT[A/G]TGTGTGTGTTTTCAG	10342
rs751878413	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100714098	TGTGTTATTTTGCCC[A/G]TTTTTATTGGACTCT	10342
rs751879716	in-del	-/AAATC			intron-variant	TFG	GRCh38.p7	3:100723481	ATGGAATTTTAAAAA[-/AAATC]CAGTTCCATGCTACT	10342
rs751918979	snp	A/C			intron-variant	TFG	GRCh38.p7	3:100715315	ATTGGCAAGCAGATG[A/C]GTGAAGACAGAGTAT	10342
rs751968052	snp	C/T	1.70536e-05	0.00292002	synonymous-codon	TFG	GRCh38.p7	3:100748522	CCAACCTGGACCTGG[C/T]TATCGATAAGGAGGC	10342
rs752017367	snp	C/T	1.64925e-05	0.00287158	synonymous-codon	TFG	GRCh38.p7	3:100728806	GAATCGTTTATTGGA[C/T]AGCTTGGAACCACCT	10342
rs752036404	snp	G/T			intron-variant	TFG	GRCh38.p7	3:100712640	ATGACTGTTGTCTGC[G/T]AGGCACTGTTGTAGA	10342
rs752127715	snp	A/C			intron-variant	TFG	GRCh38.p7	3:100741070	CACATAATTATGGGT[A/C]GTACCTAATACTTGA	10342
rs752170335	in-del	-/C			downstream-variant-500B	TFG, ABI3BP	GRCh38.p7	3:100749090	CTAACTTACAGATTT[-/C]CATTCAGAGAAAACA	10342
rs752177985	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100728005	ACTTGGCTAATTTTT[C/T]AAGGTTTTTGTAGAG	10342
rs752241457	snp	A/G	1.6736e-05	0.0028927	missense	TFG	GRCh38.p7	3:100748503	CCTTTGGTCAGGGCT[A/G]TACCCAACCTGGACC	10342
rs752280328	in-del	-/TTTT	1.69039e-05	0.00290717	intron-variant	TFG	GRCh38.p7	3:100736558	GGATACTAAACTGAC[-/TTTT]TTTTGACTATCCAGG	10342
rs752281521	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100740010	AATTGTTTCAAGATT[C/T]GTTTGTTAAATTGAC	10342
rs752292956	snp	A/G	1.64887e-05	0.00287125	missense	TFG	GRCh38.p7	3:100728784	TGATAGAACTTCGAA[A/G]TAAAGTGAATCGTTT	10342
rs752362534	snp	A/C			intron-variant	TFG	GRCh38.p7	3:100729289	TGGAAGTATTTTCAA[A/C]TAAAAATCACTTAGA	10342
rs752417508	snp	G/T	1.67075e-05	0.00289023	intron-variant	TFG	GRCh38.p7	3:100728876	AAACCCTGAATCCAT[G/T]GTATTCTGACTTATT	10342
rs752451749	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100717938	ATTTTTTATTTTTTT[A/G]TCTTGAGACAGGGTC	10342
rs752480195	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100727918	CAGCCAACTGGACTT[C/T]CCCTCCCGGGATCAA	10342
rs752506772	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100716779	CCTGATATGTGTGCA[C/T]TTCCCTGATGATTTG	10342
rs752525957	snp	A/G			downstream-variant-500B, utr-variant-3-prime	TFG, ABI3BP	GRCh38.p7	3:100749358	AAACTACATCTCTTT[A/G]TTGCAGAATTTATAC	10342
rs752551115	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100730096	TGAAAAAGTTAGACA[A/G]TTTTTCCAGAAGAAT	10342
rs752589628	snp	A/T	1.80977e-05	0.00300808	intron-variant	TFG	GRCh38.p7	3:100748101	AATTCTTTGGAAAAG[A/T]AGTTTTACTAAAAGA	10342
rs752613620	snp	G/T			intron-variant	TFG	GRCh38.p7	3:100735496	GAATTAGTATATCCT[G/T]TGTACAGATGAGGAA	10342
rs752617677	snp	C/G			intron-variant	TFG	GRCh38.p7	3:100728451	AAAAAGTAGAGCTCG[C/G]ATTTTCCTACCAAAC	10342
rs752678301	snp	A/G			upstream-variant-2KB	TFG	GRCh38.p7	3:100707347	GGGAAATTACAACAT[A/G]AAGAGCCTCAAGTTG	10342
rs752762145	snp	C/T	3.29603e-05	0.00405944	missense	TFG	GRCh38.p7	3:100744884	ATGGTGCACAGCAGC[C/T]GCAGGCTCCACCTCA	10342
rs752787175	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100714254	CCTGTAATCCCAGCA[C/T]TTTGGGAGACCGAGG	10342
rs752840628	snp	A/T			intron-variant	TFG	GRCh38.p7	3:100713061	ACTAGGTTTTACTTA[A/T]CAGTGTTAACTCTGG	10342
rs752850223	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100745789	GGCCAAATCTGGACT[A/G]TTGCCTGTTTTTTTG	10342
rs752852103	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100721275	AAGGGAAATATCCAG[A/G]GAACAAAAAAGTAGA	10342
rs752939341	in-del	-/AAAG			intron-variant	TFG	GRCh38.p7	3:100724847	AGATCATCTCTAGAT[-/AAAG]AAAAGCCATTCATAT	10342
rs752977830	snp	G/T			intron-variant	TFG	GRCh38.p7	3:100721302	TAGAGGGAACTAAAG[G/T]CCTGATGTACCAAAA	10342
rs752996611	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100712038	ATTAAGATAAGCATG[A/G]CATCCCTAGAGTGGA	10342
rs753018198	snp	A/T			intron-variant	TFG	GRCh38.p7	3:100715095	TTTTACCTCTTAACA[A/T]CTCTGACACTGCTTA	10342
rs753055588	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100735923	AGTATGAGTTAACAA[A/G]AGTAAACTAGATAGA	10342
rs753131570	in-del	-/T			intron-variant	TFG	GRCh38.p7	3:100734673	TGGATTTACTTTGCC[-/T]TTATCAGTAGTTGGA	10342
rs753204924	snp	A/G			upstream-variant-2KB	TFG	GRCh38.p7	3:100709182	AAACCACTTAAAGTT[A/G]GACAGACGTCTACTG	10342
rs753259754	snp	A/G	0.000280179	0.0118326	missense	TFG	GRCh38.p7	3:100748407	GGGCCTATCAACCAA[A/G]ACCAGGTTTTACTTC	10342
rs753375115	snp	C/T	0.00013295	0.00815214	missense	TFG	GRCh38.p7	3:100748272	AACTGCCTGCTCAGC[C/T]GCCACAGCAGTACCA	10342
rs753411578	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100729451	TCAACATTTGGAACT[A/G]ACATAATTTTGGGAC	10342
rs753425220	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100735409	ATAAGCTTTTGCTGT[A/G]TAATTCCTTTTATAA	10342
rs753441024	snp	C/T	1.64887e-05	0.00287125	synonymous-codon	TFG	GRCh38.p7	3:100748378	TCAACCTGGAATGGC[C/T]CCAAGCCAACCTGGG	10342
rs753456081	snp	A/G	0.0002836	0.0119046	intron-variant	TFG	GRCh38.p7	3:100720094	TGAATTTACTATTTT[A/G]TTCATTGTATTTTAA	10342
rs753581066	snp	C/G			upstream-variant-2KB	TFG	GRCh38.p7	3:100708137	ACCTAGCTTAACAGA[C/G]AAGATTGAAAACCTA	10342
rs753634042	snp	G/T			upstream-variant-2KB	TFG	GRCh38.p7	3:100707396	TCCATGAGCTCCAGC[G/T]TTTCCACAAGGCCAG	10342
rs753673346	snp	C/G			intron-variant	TFG	GRCh38.p7	3:100718784	GCTGGTCTCGAACTC[C/G]TGACCTCAGGTGATC	10342
rs753789196	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100738600	GTCCACAGCAACCAA[A/G]TTCCTTTTTTCAGAG	10342
rs753841176	snp	A/T	1.64893e-05	0.0028713	missense	TFG	GRCh38.p7	3:100736660	CTCACCCACCAGGCG[A/T]TCAGCCACAGCAGCC	10342
rs753850050	in-del	-/TAAG			intron-variant	TFG	GRCh38.p7	3:100714708	GATTTTATGGTCAAC[-/TAAG]TAAGGGAAAGCTGGT	10342
rs753896613	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100733680	TGTCTGATAGTGTTT[A/G]GTTGAAAACTAGACA	10342
rs753897840	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100746088	ATTGTATAAAATACA[C/T]AGAACTTAAGTTTGG	10342
rs753936141	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100747090	CAAATTATTATCTTT[A/G]TATTTCTGATCCTAC	10342
rs753951057	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100720558	CATGTGCAATTCACA[A/G]TAGGGTTCACACTCC	10342
rs753963694	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100741895	CTGCTATGTACCATA[C/T]AGCCTAGCTATGTAG	10342
rs753980451	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100715187	ATGCCAGCAGATATA[A/G]TAGAAATCTTAAAAT	10342
rs754111575	snp	A/T			intron-variant, upstream-variant-2KB, utr-variant-5-prime	TFG	GRCh38.p7	3:100710285	AAGAGTTTGCTTTGC[A/T]GGACACTACAGTAAG	10342
rs754169542	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100723665	TAATTCACTAGGACT[A/G]TATAGCAATCTGAAC	10342
rs754187991	snp	A/G	1.65195e-05	0.00287393	missense	TFG	GRCh38.p7	3:100732625	ACCAAGATGAAATCA[A/G]TAAAAATGTTATGTC	10342
rs754241191	snp	C/T	1.7472e-05	0.00295562	intron-variant	TFG	GRCh38.p7	3:100732713	ACCCTTCGTTTCCTT[C/T]ATCTTTCCGTTCTTC	10342
rs754332825	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100741343	AATGATCCTGATGCT[A/G]TATAGGCCTAGGCTA	10342
rs754405501	in-del	-/TA			intron-variant	TFG	GRCh38.p7	3:100741945	TTTGTGTAAGTATAC[-/TA]TATGATTATACAGTG	10342
rs754467437	snp	A/C			intron-variant	TFG	GRCh38.p7	3:100746500	TAAAAGGCTAGATGT[A/C]CTATGTATTAAAAAA	10342
rs754512804	in-del	-/AAAA			intron-variant	TFG	GRCh38.p7	3:100713908	TTTTAAAGTCTTTTT[-/AAAA]AAAAAAAAAAAAAGA	10342
rs754581149	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100727826	TGCATATATTTTTAA[A/G]TTTATATTTATTTTT	10342
rs754592602	snp	C/T	1.67055e-05	0.00289006	intron-variant	TFG	GRCh38.p7	3:100720099	TTACTATTTTATTCA[C/T]TGTATTTTAAAGATG	10342
rs754670520	in-del	-/T			intron-variant	TFG	GRCh38.p7	3:100736558	GGATACTAAACTGAC[-/T]TTTTTTTGACTATCC	10342
rs754749470	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100746269	CACCTGGGGGAGGCT[A/G]TGTGTGGGGCCCCAT	10342
rs754768452	snp	A/T			intron-variant	TFG	GRCh38.p7	3:100738093	ACAAAGCCAAAAAAA[A/T]AAAAATCCACAGAGT	10342
rs754775791	snp	G/T			intron-variant	TFG	GRCh38.p7	3:100715442	GCTAAGATGCAAATG[G/T]GTTGGGAAGTATAGT	10342
rs754932789	snp	G/T			downstream-variant-500B	TFG, ABI3BP	GRCh38.p7	3:100749155	ATGCATTTGGTAATC[G/T]TTGGTTTAAAATGAA	10342
rs754985791	snp	C/T			utr-variant-3-prime	TFG	GRCh38.p7	3:100748807	GACTTTCTAGCTTCC[C/T]TTGTCCGGAGGATAT	10342
rs755002578	snp	C/G	1.64784e-05	0.00287035	missense	TFG	GRCh38.p7	3:100744837	TGTGTTTTCAGGTCA[C/G]ATGTACCAACAGTAC	10342
rs755013539	snp	A/C			intron-variant	TFG	GRCh38.p7	3:100712956	GTAGGAAATGAAGTT[A/C]AATACTTGGCCAGGG	10342
rs755200692	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100718889	TTTTGATTTGTGTCC[A/G]TTAGATTCTGTTAGT	10342
rs755242228	snp	A/C/G	9.92825e-05	0.00704503	missense	TFG	GRCh38.p7	3:100732636	ATCAATAAAAATGTT[A/C/G]TGTCAGCGTTTGGCT	10342
rs755353690	in-del	-/T			intron-variant	TFG	GRCh38.p7	3:100718104	TTCTTATTCTTAATG[-/T]TTATCAAAATGGGGG	10342
rs755364960	snp	C/T	0.000123985	0.00787255	intron-variant	TFG	GRCh38.p7	3:100732721	TTTCCTTCATCTTTC[C/T]GTTCTTCCCTTTCCT	10342
rs755394014	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100721162	ACTAGGCATAAAGCA[A/G]ATTAGATAATCTGAA	10342
rs755469234	snp	C/T			synonymous-codon	TFG	GRCh38.p7	3:100732512	TATTTTTACAGATAC[C/T]GTGGATGGTAGGGAA	10342
rs755490448	snp	C/G			upstream-variant-2KB	TFG	GRCh38.p7	3:100708342	ATAAATCTTCCACCA[C/G]GTGGCTCTGCTGGAG	10342
rs755514457	in-del	-/CA			intron-variant	TFG	GRCh38.p7	3:100733613	TGGGTTCCTCTCCCC[-/CA]CACACACTCCCCCCA	10342
rs755634269	snp	C/T			missense	TFG	GRCh38.p7	3:100748320	CACAAACTTACACTG[C/T]CCAAACTTCTCAGCC	10342
rs755641091	snp	G/T			intron-variant	TFG	GRCh38.p7	3:100728165	AACGATTTCTTTTAA[G/T]ATCAGCTATTTTAGT	10342
rs755717705	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100716803	TGATTTGTGATTTTG[A/G]GCATTTTTTCATATA	10342
rs755728694	snp	C/T	3.33023e-05	0.00408044	missense	TFG	GRCh38.p7	3:100748250	GCCTTTTCTGGTCAG[C/T]CTCAACAACTGCCTG	10342
rs755756124	in-del	-/ACACCAATTAA	1.74418e-05	0.00295307	utr-variant-3-prime	TFG	GRCh38.p7	3:100748543	TAAGGAGGCTCCTCT[-/ACACCAATTAA]ACACCAATTAATGTA	10342
rs755767571	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100748050	TACATATTTATTAAA[C/T]TTCTCACCATTTTTG	10342
rs755785221	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100731745	TATTTTTGGTAGAGA[C/T]TGGGTTTTGCCAGGC	10342
rs755786028	in-del	-/TATTTTT			intron-variant	TFG	GRCh38.p7	3:100742007	AGCAATGCATGACCA[-/TATTTTT]TATTTTTTATTACTC	10342
rs755824460	snp	C/G			intron-variant	TFG	GRCh38.p7	3:100719953	AAATTAAAAAACAAC[C/G]TTTTTTTTTTTTAAA	10342
rs755835566	snp	A/T	1.66136e-05	0.00288211	intron-variant	TFG	GRCh38.p7	3:100720078	GTAGTAAACTTTCTA[A/T]TGAATTTACTATTTT	10342
rs756086157	in-del	-/A			intron-variant	TFG	GRCh38.p7	3:100741389	TCATAATTTTTTTCT[-/A]AATGTTTAAAAAAGT	10342
rs756099155	in-del	-/A	1.65113e-05	0.00287322	intron-variant	TFG	GRCh38.p7	3:100736723	GATTGAAGGTAAAAT[-/A]AGAGTTTAGAACACA	10342
rs756131903	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100735671	AAGGAATAAGACATA[C/T]TTACATTGTCCTCAG	10342
rs756172934	snp	C/T	1.67447e-05	0.00289345	intron-variant	TFG	GRCh38.p7	3:100736534	CTTGCTGGGGGAAGG[C/T]CTTGTGTTGGATACT	10342
rs756303367	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100714265	AGCACTTTGGGAGAC[C/T]GAGGTAGGCGGATCA	10342
rs756327717	snp	C/T	1.7505e-05	0.00295841	utr-variant-3-prime	TFG	GRCh38.p7	3:100748547	GGAGGCTCCTCTACA[C/T]CAATTAATGTAGCTG	10342
rs756431310	snp	G/T			intron-variant	TFG	GRCh38.p7	3:100722400	AGAAGTTGAAAATGA[G/T]AACATCCAGAATATT	10342
rs756503382	snp	A/G	3.46476e-05	0.00416204	intron-variant	TFG	GRCh38.p7	3:100732461	TAGGCCTTACTGAAT[A/G]TAGATAAAAAGGAAA	10342
rs756555265	snp	C/G			intron-variant	TFG	GRCh38.p7	3:100721403	TGGTGTCTACATGGT[C/G]TAGGCCCTTGGTCCT	10342
rs756556370	snp	A/T	1.65179e-05	0.00287379	missense	TFG	GRCh38.p7	3:100732622	AAAACCAAGATGAAA[A/T]CAATAAAAATGTTAT	10342
rs756716497	snp	C/G			intron-variant	TFG	GRCh38.p7	3:100718594	ACAAAGTCTTGCTTT[C/G]TCGTTTAGGCTGGAG	10342
rs756768135	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100717024	TTTCCTTTGCTGTGC[A/G]GAAAAGTTTTCCAGT	10342
rs756789337	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100718187	CTGCCTTGGCCTGCC[A/G]AAGTACTGAGATTAC	10342
rs756844330	snp	A/C			upstream-variant-2KB	TFG	GRCh38.p7	3:100707435	TGCCTCTCTTCCTAG[A/C]GTACAGATGACCACA	10342
rs756879809	snp	C/G			intron-variant	TFG	GRCh38.p7	3:100730380	TTTACCTATGTTAAT[C/G]TAAAAGGTGTTAAAA	10342
rs756895173	snp	A/T	1.64806e-05	0.00287054	synonymous-codon	TFG	GRCh38.p7	3:100744873	ACAGGCCGGCTATGG[A/T]GCACAGCAGCCGCAG	10342
rs756903764	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100735752	TTCATTTCTGTGTTC[A/G]TTATTTTGTAAGAAT	10342
rs756950367	snp	C/T	1.76546e-05	0.00297102	intron-variant	TFG	GRCh38.p7	3:100748131	ATAAGATACATGTTA[C/T]TTATTTTGCCTTTTC	10342
rs756989102	in-del	-/CT			intron-variant	TFG	GRCh38.p7	3:100744503	CTGATTTTCAACTCA[-/CT]TGGCTTTTAATGAAC	10342
rs757062394	in-del	-/T	3.34655e-05	0.00409043	intron-variant	TFG	GRCh38.p7	3:100736767	ACATGTGTAGAAGTG[-/T]TTATTACAGCATTGT	10342
rs757071170	snp	A/C	1.65274e-05	0.00287462	intron-variant	TFG	GRCh38.p7	3:100713888	AGAGTGTTTTTAAAG[A/C]TATTTTTTAAAGTCT	10342
rs757115704	in-del	-/ATATA			intron-variant	TFG	GRCh38.p7	3:100716104	TAGCTATTTGAAATT[-/ATATA]ATATGTTATTGTTAA	10342
rs757183417	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100742127	TTCTTTTTTTAAACA[A/G]TTAAACAGACTTCTT	10342
rs757212703	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100726294	AAACTTATCCTACCT[C/T]CTTCTGCCTGTTTTG	10342
rs757265695	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100724995	TGCAAGCTCCGCCTC[C/T]GGGGCTCACCCCATT	10342
rs757292239	snp	A/T			upstream-variant-2KB	TFG	GRCh38.p7	3:100708283	ATCCAGCTGTTTCTG[A/T]ACTTCACTGCCAATT	10342
rs757343326	snp	G/T			intron-variant	TFG	GRCh38.p7	3:100747136	AATTTGATTGAGAGA[G/T]ATGGAAATAGTCAAC	10342
rs757477171	snp	C/G			intron-variant	TFG	GRCh38.p7	3:100721780	CTAATAGCAGGATTA[C/G]ATTTTCAACAACTTC	10342
rs757575632	in-del	-/AACTA			downstream-variant-500B	TFG, ABI3BP	GRCh38.p7	3:100749072	AAGTATAAACATTTT[-/AACTA]AACTAACTTACAGAT	10342
rs757661070	snp	A/C/T	5.14093e-05	0.00506976	synonymous-codon, stop-gained	TFG	GRCh38.p7	3:100748526	CCTGGACCTGGTTAT[A/C/T]GATAAGGAGGCTCCT	10342
rs757712332	snp	A/G	4.95094e-05	0.00497517	missense	TFG	GRCh38.p7	3:100728808	ATCGTTTATTGGATA[A/G]CTTGGAACCACCTGG	10342
rs757856523	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100741353	ATGCTGTATAGGCCT[A/G]GGCTAATGTGTATGT	10342
rs757985623	in-del	-/T			utr-variant-3-prime, downstream-variant-500B	TFG, ABI3BP	GRCh38.p7	3:100748859	GCCATCTTACTTGGC[-/T]TTTTTACTATTAACA	10342
rs758011641	snp	C/T	1.64901e-05	0.00287137	missense	TFG	GRCh38.p7	3:100728795	CGAAATAAAGTGAAT[C/T]GTTTATTGGATAGCT	10342
rs758015143	in-del	-/AA			intron-variant	TFG	GRCh38.p7	3:100713908	TTTTAAAGTCTTTTT[-/AA]AAAAAAAAAAAAAAA	10342
rs758059257	snp	A/T			intron-variant	TFG	GRCh38.p7	3:100740012	TTGTTTCAAGATTCG[A/T]TTGTTAAATTGACTT	10342
rs758121354	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100747047	AAATTTAGTCAGGGT[C/T]TTCACTCTGAGTAAA	10342
rs758183860	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100726439	CACCCAGAAACAGTA[C/T]TTTACCAGCCATCTA	10342
rs758264624	snp	G/T	1.80361e-05	0.00300295	intron-variant	TFG	GRCh38.p7	3:100748110	GAAAAGTAGTTTTAC[G/T]AAAAGATAAGATACA	10342
rs758305155	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100715272	TTACCTTCAACACAT[A/G]GCTTATAAGCTCACC	10342
rs758360186	snp	G/T			intron-variant	TFG	GRCh38.p7	3:100727732	CTAGAGATTACCGAG[G/T]AATCTCTGGCATTTT	10342
rs758417817	snp	C/T	1.73845e-05	0.00294821	intron-variant	TFG	GRCh38.p7	3:100713882	AAGGTAAGAGTGTTT[C/T]TAAAGCTATTTTTTA	10342
rs758464718	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100735441	CCCATGCTATAAGCT[C/T]TTGTAAACTCATAAT	10342
rs758524457	snp	A/G	1.65647e-05	0.00287786	synonymous-codon	TFG	GRCh38.p7	3:100732641	TAAAAATGTTATGTC[A/G]GCGTTTGGCTTAACA	10342
rs758565539	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100711557	GGTACAGTGTGAGGG[A/G]TCGGATGTAAAAACT	10342
rs758797968	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100712680	TATGGAAAACATAAT[C/T]GTTTACTTCCTACCA	10342
rs758853852	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100712066	GGAATGCAGTTCACT[C/T]TGTTCTGCATTGACC	10342
rs758854451	snp	G/T			intron-variant	TFG	GRCh38.p7	3:100734366	CCAGCCCTATAGTCA[G/T]CTGGGGATTTGGACA	10342
rs758860090	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100742962	ACTGTGGTTTTGACC[A/G]GGAGTTCCTTACTCA	10342
rs758874813	snp	A/C	1.67809e-05	0.00289658	missense	TFG	GRCh38.p7	3:100748506	TTGGTCAGGGCTATA[A/C]CCAACCTGGACCTGG	10342
rs758909505	snp	C/G			intron-variant	TFG	GRCh38.p7	3:100735962	AGTAGAAAAAGTATT[C/G]ATGAGTCAAGAAGGC	10342
rs758930003	snp	G/T			intron-variant	TFG	GRCh38.p7	3:100731703	CTGGGATTACAGGCA[G/T]GCATCACTGTGCCTA	10342
rs758934125	snp	G/T			intron-variant	TFG	GRCh38.p7	3:100718320	ACTGTTTAGGGCAAA[G/T]GTCAGCAAACATTTT	10342
rs758939134	snp	G/T	9.89038e-05	0.00703151	missense	TFG	GRCh38.p7	3:100748415	CAACCAAGACCAGGT[G/T]TTACTTCACTTCCTG	10342
rs758985034	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100730631	GCCAATCAGCTATCA[A/G]TGCTATTTAGAACCT	10342
rs759009062	snp	G/T			intron-variant	TFG	GRCh38.p7	3:100735079	ATAAATATATATATT[G/T]AGGCTAATAACAGTG	10342
rs759020275	snp	C/T	3.52156e-05	0.00419602	intron-variant	TFG	GRCh38.p7	3:100728670	ATTAGTATACTTATT[C/T]ATGAACTTCTAATTT	10342
rs759028594	snp	C/T	1.7321e-05	0.00294282	utr-variant-5-prime	TFG	GRCh38.p7	3:100713656	AGTCTTTCTCTAGAG[C/T]TGTATATATAGAACA	10342
rs759062638	in-del	-/GAAAG	3.31049e-05	0.00406834	intron-variant	TFG	GRCh38.p7	3:100744945	AGGTGAGCAGGTGTT[-/GAAAG]GGAGTTGGCTCATGG	10342
rs759068709	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100740852	ACATAAAACATAGCT[C/T]ATATATAGTCATGCA	10342
rs759129253	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100722190	CATAAGAGCAAGATG[C/T]TATTGTATTATGGAA	10342
rs759168672	snp	C/T	1.64909e-05	0.00287144	synonymous-codon	TFG	GRCh38.p7	3:100728768	TATCTCCGTCGAGAA[C/T]TGATAGAACTTCGAA	10342
rs759196593	snp	A/G	1.66713e-05	0.0028871	missense	TFG	GRCh38.p7	3:100748497	GTCCTCCCTTTGGTC[A/G]GGGCTATACCCAACC	10342
rs759200856	snp	A/G			intron-variant, upstream-variant-2KB	TFG	GRCh38.p7	3:100710838	GAACTAGTTAATACC[A/G]GTCTCTACTTTGGAA	10342
rs759324975	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100729981	GAGATCCTCTTGGTC[A/G]CTTTATGATGAAACC	10342
rs759372341	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100729093	CTACTGGAGCGTAGC[A/G]CCTGGAAATCCCATT	10342
rs759426050	snp	G/T			intron-variant	TFG	GRCh38.p7	3:100742206	TGGGTTTAAAGTAAG[G/T]ACCGTAAATCCTCAC	10342
rs759500423	snp	C/T	4.27168e-05	0.00462132	intron-variant	TFG	GRCh38.p7	3:100719933	TACAAATCTGAAAAT[C/T]TAAAAAATTAAAAAA	10342
rs759578675	snp	A/G	1.65173e-05	0.00287374	synonymous-codon	TFG	GRCh38.p7	3:100748309	CAATTATCCTGCACA[A/G]ACTTACACTGCCCAA	10342
rs759635605	snp	A/G			upstream-variant-2KB	TFG	GRCh38.p7	3:100708771	TCTCCCTTGCCCCTG[A/G]TATTTCCTCTTAGTA	10342
rs759642479	in-del	-/T			intron-variant	TFG	GRCh38.p7	3:100738099	CCAAAAAAAAAAAAA[-/T]CCACAGAGTTGTCTG	10342
rs759739396	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100738401	AGTGTATACTGTGAT[A/G]CAATGACAGTTGGAA	10342
rs759794499	in-del	-/G	0.000643439	0.017925	splice-acceptor-variant	TFG	GRCh38.p7	3:100713642	AAACCACTTTTATCA[-/G]TCTTTCTCTAGAGTT	10342
rs759843478	in-del	-/A			intron-variant	TFG	GRCh38.p7	3:100733964	TGTTTTGAAATAATT[-/A]TTGTTGGCTACAAAG	10342
rs759899065	snp	A/G	1.64977e-05	0.00287203	synonymous-codon	TFG	GRCh38.p7	3:100736607	TGCAGAAGATCGTTC[A/G]GGAACACCCGACAGC	10342
rs759966634	snp	A/T			intron-variant	TFG	GRCh38.p7	3:100733593	TGGAGTCAGTTTCTA[A/T]TGACTGGGTTCCTCT	10342
rs760040607	snp	C/G			intron-variant	TFG	GRCh38.p7	3:100746734	AATAATTAAGGATCA[C/G]ATTACTTCCAGGCCC	10342
rs760041026	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100734266	CTATGGTGTATAGCA[A/G]CTGATATGTATGCTC	10342
rs760089237	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100712173	AGGGGTCTAGAGATA[C/T]TAATTTAAGGACTAG	10342
rs760146685	snp	C/T	1.65059e-05	0.00287275	missense	TFG	GRCh38.p7	3:100736591	GGCCACCCAGTGCTC[C/T]TGCAGAAGATCGTTC	10342
rs760197199	snp	C/G			intron-variant	TFG	GRCh38.p7	3:100730197	TAGATGAGAATTTAA[C/G]CAGTATAGCCAATAC	10342
rs760211948	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100724382	AAACTTTAAAAATTT[A/G]TATATACCATGAATT	10342
rs760232443	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100735189	CATTTTATTTTGGCA[A/G]TCATCAGTCTCTCTT	10342
rs760303712	snp	A/C	1.64893e-05	0.0028713	missense	TFG	GRCh38.p7	3:100748373	GCCTCTCAACCTGGA[A/C]TGGCTCCAAGCCAAC	10342
rs760416726	in-del	-/T	0.000130031	0.00806216	intron-variant	TFG	GRCh38.p7	3:100713903	CTATTTTTTAAAGTC[-/T]TTTTAAAAAAAAAAA	10342
rs760449533	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100718738	GATTTTTGTATTTTT[A/G]GTAGAGACGGAGTTT	10342
rs760506542	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100718049	TGCAACTCAGCCTCC[C/T]GTGTAGCTGGGACTG	10342
rs760538512	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100711733	GCTGGTTTACACTTC[C/T]TGTAGGAAGGAGAAG	10342
rs760541258	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100720168	ACTTATTCAAATATT[A/G]TTACATTTATTTGTG	10342
rs760562204	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100731477	TTTAAACATTTTATT[A/G]TAGAAAAGTTTAAGT	10342
rs760595911	snp	C/G	1.65982e-05	0.00288077	missense	TFG	GRCh38.p7	3:100728852	TCCACCAATATTCCT[C/G]AAAATGGTAAACCCT	10342
rs760607344	snp	C/T	0.000755654	0.0194231	intron-variant	TFG	GRCh38.p7	3:100713903	CTATTTTTTAAAGTC[C/T]TTTTAAAAAAAAAAA	10342
rs760613274	snp	C/T	1.64944e-05	0.00287175	stop-gained	TFG	GRCh38.p7	3:100728762	GTGAAATATCTCCGT[C/T]GAGAACTGATAGAAC	10342
rs760798289	in-del	-/T	0.0112403	0.0741201	intron-variant	TFG	GRCh38.p7	3:100719954	AATTAAAAAACAACC[-/T]TTTTTTTTTTTAAAT	10342
rs760824621	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100715153	TTTCTCTGTCTGTGT[C/T]AGGGTTGGGCTTAAA	10342
rs760849944	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100746829	AGTGTTAAAATGAAT[A/G]GGCATTTTCAGTATA	10342
rs760894126	snp	C/G	1.66054e-05	0.00288139	missense	TFG	GRCh38.p7	3:100748178	CAGACTGGACCTCAA[C/G]AACCTCAGCAGTTCC	10342
rs760922330	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100716297	TTTAGCTTCCACATA[C/T]GAGAGAGAGCATGTG	10342
rs760933284	in-del	-/ATAA			intron-variant	TFG	GRCh38.p7	3:100739065	AGAGCACAGCTTTAG[-/ATAA]ATATAGTCGTTATTT	10342
rs761025851	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100735202	CAATCATCAGTCTCT[C/T]TTGCATTACCACTAT	10342
rs761043626	snp	A/T	0.000191644	0.009787	intron-variant	TFG	GRCh38.p7	3:100713911	TAAAGTCTTTTTAAA[A/T]AAAAAAAAAAAAAGA	10342
rs761080881	snp	C/T			utr-variant-3-prime	TFG	GRCh38.p7	3:100748771	GGAACACTACTCTTA[C/T]ATGTATAAAGTGATT	10342
rs761238366	snp	C/T	6.89869e-05	0.00587271	intron-variant	TFG	GRCh38.p7	3:100732704	CTCCTTTACACCCTT[C/T]GTTTCCTTCATCTTT	10342
rs761340524	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100713465	GACGTAAAATAAAAG[C/T]TTATTTTATTATCCC	10342
rs761357419	snp	A/G	1.64958e-05	0.00287187	missense	TFG	GRCh38.p7	3:100732573	CAGTCTACTCAGGTT[A/G]TGGCAGCAAGTATGT	10342
rs761436238	in-del	-/A			intron-variant	TFG	GRCh38.p7	3:100742398	ATGTGAGTTATAGAT[-/A]ACATTTAAGAAAGAT	10342
rs761455928	in-del	-/C			intron-variant	TFG	GRCh38.p7	3:100730293	TAGGTGAAACTTTTT[-/C]CCTCACCTCTTTCTT	10342
rs761558430	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100745290	GTAACACGTAATTCC[A/G]GTGTACTCTTAGTAC	10342
rs761558908	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100731666	GGTTCAAGTGATTCT[C/T]GTGACTCAGCCTCCT	10342
rs761586874	snp	G/T			upstream-variant-2KB	TFG	GRCh38.p7	3:100709282	CTTTCGAGAAAACCG[G/T]AAGTGCGTGGTCACG	10342
rs761683764	snp	G/T	9.90181e-05	0.00703557	synonymous-codon	TFG	GRCh38.p7	3:100748330	CACTGCCCAAACTTC[G/T]CAGCCTACTAATTAT	10342
rs761786549	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100734917	TAGCTAGGATACTTT[C/T]GTAGTTCTTCAGGTG	10342
rs761808608	snp	A/G	3.3173e-05	0.00407252	intron-variant	TFG	GRCh38.p7	3:100720068	TATTTGGTGAGTAGT[A/G]AACTTTCTAATGAAT	10342
rs761808737	snp	A/G	9.92178e-05	0.00704266	synonymous-codon	TFG	GRCh38.p7	3:100748474	GCCTAATCCTTATGC[A/G]CGTAACCGTCCTCCC	10342
rs761819172	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100738634	GCAGATTAACACTGT[C/T]TATATGCATTTAATT	10342
rs761969042	in-del	-/AAC			downstream-variant-500B	TFG, ABI3BP	GRCh38.p7	3:100749319	CATTCAGAAATAACA[-/AAC]AACAAAAACTCAATC	10342
rs761992713	in-del	-/CTAG			utr-variant-3-prime	TFG	GRCh38.p7	3:100748797	GATTGACTTGACTTT[-/CTAG]CTAGCTTCCCTTGTC	10342
rs762052285	snp	C/G			intron-variant	TFG	GRCh38.p7	3:100735389	TCTGAGTAGTAGTCA[C/G]TTTTATAAGCTTTTG	10342
rs762071964	snp	G/T	1.64838e-05	0.00287083	intron-variant	TFG	GRCh38.p7	3:100744821	CTTGTGTGTGTGTGT[G/T]TGTGTTTTCAGGTCA	10342
rs762104730	snp	C/T			utr-variant-3-prime, downstream-variant-500B	TFG, ABI3BP	GRCh38.p7	3:100748930	ATGTATAAAATGTAA[C/T]ACTGATGATAGGTTA	10342
rs762125227	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100725734	GGAGGCAGAGGTTGC[A/G]GTGAGCCAAGATCAG	10342
rs762164186	snp	A/T	3.39749e-05	0.00412144	utr-variant-5-prime	TFG	GRCh38.p7	3:100713680	TAGAACATCCTGGAG[A/T]CCACCATGAACGGAC	10342
rs762194108	snp	C/G	6.63383e-05	0.00575888	intron-variant	TFG	GRCh38.p7	3:100744950	AGCAGGTGTTGAAAG[C/G]GAGTTGGCTCATGGT	10342
rs762247551	snp	A/C	1.65872e-05	0.00287981	missense	TFG	GRCh38.p7	3:100713827	GTTTTCAGAGGAAAA[A/C]TTCTGAGTAATGATG	10342
rs762248597	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100712451	TAGAATGTGGCCAGT[A/G]GTAGTTTGTAGGATA	10342
rs762265045	in-del	-/ATTC	5.00588e-05	0.00500269	intron-variant	TFG	GRCh38.p7	3:100720094	TGAATTTACTATTTT[-/ATTC]ATTGTATTTTAAAGA	10342
rs762325030	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100717898	TAATTGCTCTGGCTA[A/G]TACTTGCTTAACTGT	10342
rs762673065	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100740673	TCATAAATGCTATAC[A/G]TGTGCAGAAGCCGTT	10342
rs762789381	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100739757	TGCTGGAGTAGTTTA[A/G]ATCAAATTATGAACA	10342
rs762834955	snp	A/C			utr-variant-5-prime, upstream-variant-2KB	TFG	GRCh38.p7	3:100709412	GCCCTGCGCCTCGCG[A/C]CGTCGCGCATGCGTC	10342
rs762919188	in-del	-/C			intron-variant	TFG	GRCh38.p7	3:100711388	TACAGGTGTGAGCCA[-/C]CCGTGCCCGGCCCTC	10342
rs762932536	snp	A/C	1.66023e-05	0.00288113	missense	TFG	GRCh38.p7	3:100748192	ACAACCTCAGCAGTT[A/C]CAGGGATATGGCCAG	10342
rs762952687	in-del	-/TTT			intron-variant	TFG	GRCh38.p7	3:100732129	TAGTTCCTATAATTA[-/TTT]TTTCCAGAGTGCCCA	10342
rs763052199	in-del	-/AAAC			intron-variant	TFG	GRCh38.p7	3:100738072	GAGACCCTGTCTCAA[-/AAAC]AAACAAAGCCAAAAA	10342
rs763069975	snp	C/T			upstream-variant-2KB	TFG	GRCh38.p7	3:100708024	AAACACCAGAATTTA[C/T]TCCAGGTCCTTTAGG	10342
rs763129513	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100748052	CATATTTATTAAATT[C/T]CTCACCATTTTTGGT	10342
rs763163559	in-del	-/A			intron-variant	TFG	GRCh38.p7	3:100725623	CTCTACCAAAAATAC[-/A]AAAAAAAAAAAAAAA	10342
rs763183981	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100724625	TGGGGTTAATATAAC[A/G]TTAACATGAAAACCA	10342
rs763194905	in-del	-/T			intron-variant	TFG	GRCh38.p7	3:100745899	TGCAACAGAAGACCA[-/T]TGTGGCCCACAAAGC	10342
rs763199836	snp	G/T	2.67849e-05	0.00365947	intron-variant	TFG	GRCh38.p7	3:100744809	ATGCCTTTTTTCCTT[G/T]TGTGTGTGTGTGTGT	10342
rs763216920	snp	G/T			intron-variant	TFG	GRCh38.p7	3:100738282	ACTAGAACTAAAGCA[G/T]ATGTCAGCTGAAATG	10342
rs763264826	snp	A/T			intron-variant	TFG	GRCh38.p7	3:100725442	GATTTAATTATGTCT[A/T]TGCTGTTTCATTTCT	10342
rs763266792	in-del	-/AATC	1.65162e-05	0.00287365	frameshift-variant	TFG	GRCh38.p7	3:100732620	AAAAAACCAAGATGA[-/AATC]AATAAAAATGTTATG	10342
rs763290821	snp	C/G	1.64893e-05	0.0028713	missense	TFG	GRCh38.p7	3:100736645	CCTCCTCCTCAGCAG[C/G]TCACCCACCAGGCGT	10342
rs763363405	in-del	-/G	1.64822e-05	0.00287068	intron-variant	TFG	GRCh38.p7	3:100744823	TGTGTGTGTGTGTGT[-/G]TGTTTTCAGGTCAGA	10342
rs763374197	in-del	-/GAA			downstream-variant-500B	TFG, ABI3BP	GRCh38.p7	3:100749056	GTTTGGTCTTAAAAT[-/GAA]GAAGTATAAACATTT	10342
rs763380407	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100744563	GGTTGGAAAACATTT[A/G]TTTTTCTAGACTTTA	10342
rs763475850	snp	C/G			intron-variant	TFG	GRCh38.p7	3:100745590	ACTTTGGCTATAATT[C/G]CAGTATTTTTTACAG	10342
rs763523148	snp	A/T	6.59435e-05	0.00574172	missense	TFG	GRCh38.p7	3:100713783	ATGAAGATATTACTT[A/T]TGATGAATTAGTGCT	10342
rs763697897	snp	G/T	1.67885e-05	0.00289724	intron-variant	TFG	GRCh38.p7	3:100728891	TGTATTCTGACTTAT[G/T]GTTCTTACGTCTTTT	10342
rs763727259	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100712231	ATGAAGAATAGTAGG[A/G]CATTAATATATAATA	10342
rs763782320	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100718050	GCAACTCAGCCTCCC[A/G]TGTAGCTGGGACTGC	10342
rs763829002	snp	C/T	1.64961e-05	0.00287189	stop-gained	TFG	GRCh38.p7	3:100732558	GATTCTTCTGGAAAA[C/T]AGTCTACTCAGGTTA	10342
rs763842843	snp	A/C			intron-variant	TFG	GRCh38.p7	3:100730239	TAGCTACAGTGGCCC[A/C]CATTCTACTCTAAGG	10342
rs763864239	snp	G/T			intron-variant	TFG	GRCh38.p7	3:100718752	TAGTAGAGACGGAGT[G/T]TCTCCATGTTGGCCA	10342
rs763914860	in-del	-/T			utr-variant-5-prime, upstream-variant-2KB	TFG	GRCh38.p7	3:100709401	GGACCCAGCCAGCCC[-/T]GCGCCTCGCGCCGTC	10342
rs763922142	in-del	-/GTT			intron-variant	TFG	GRCh38.p7	3:100720192	ATTTGTGTTCAGGTA[-/GTT]GTTTTAGATTACTTG	10342
rs763940289	snp	A/G	5.40994e-05	0.00520065	intron-variant	TFG	GRCh38.p7	3:100748111	AAAAGTAGTTTTACT[A/G]AAAGATAAGATACAT	10342
rs763995407	snp	A/C	1.66106e-05	0.00288184	missense	TFG	GRCh38.p7	3:100748208	CAGGGATATGGCCAG[A/C]AACCAACTTCCCAGG	10342
rs764032619	snp	C/G			upstream-variant-2KB	TFG	GRCh38.p7	3:100708117	ATCCTTGTGGATGAA[C/G]TGTAACCTAGCTTAA	10342
rs764168152	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100731197	TGGTAACAAAAGTGA[C/T]AATCATTGTCCCTTA	10342
rs764168184	snp	C/G			intron-variant	TFG	GRCh38.p7	3:100737295	CTGGGTTTTGATATT[C/G]TTTCACTGTAAAATG	10342
rs764202888	snp	A/C			intron-variant	TFG	GRCh38.p7	3:100715175	GGGCTTAAAGTAATG[A/C]CAGCAGATATAATAG	10342
rs764265580	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100747085	CTTTTCAAATTATTA[C/T]CTTTGTATTTCTGAT	10342
rs764376318	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100722414	AGAACATCCAGAATA[C/T]TTCTATTCAGAGTTT	10342
rs764420674	in-del	-/TT			intron-variant	TFG	GRCh38.p7	3:100740726	ACTCTGTGTAATAAA[-/TT]TAATTCCCAGAAGTC	10342
rs764503472	in-del	-/T			intron-variant	TFG	GRCh38.p7	3:100740784	CTCTTTTCCCCTTAA[-/T]TTTTTTTTATTACTT	10342
rs764567079	in-del	-/TGAT			intron-variant	TFG	GRCh38.p7	3:100739038	GCCACATGTAGCTAG[-/TGAT]TGATTATTTTAAGAG	10342
rs764609228	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100723659	AAAGAATAATTCACT[A/G]GGACTATATAGCAAT	10342
rs764626833	snp	C/T	5.04164e-05	0.00502052	synonymous-codon	TFG	GRCh38.p7	3:100748507	TGGTCAGGGCTATAC[C/T]CAACCTGGACCTGGT	10342
rs764693876	snp	A/C			intron-variant	TFG	GRCh38.p7	3:100741149	TATTTTTAAATCATT[A/C]GAGTGTACTCCTACT	10342
rs764886075	snp	A/T			intron-variant	TFG	GRCh38.p7	3:100738649	TTATATGCATTTAAT[A/T]TTTAGAGTAGTATTG	10342
rs764906439	snp	A/G	1.66818e-05	0.00288802	synonymous-codon	TFG	GRCh38.p7	3:100748498	TCCTCCCTTTGGTCA[A/G]GGCTATACCCAACCT	10342
rs764919571	snp	G/T			upstream-variant-2KB	TFG	GRCh38.p7	3:100708188	TACAATAAGCGAGTC[G/T]TGGCCAATTCCAGCC	10342
rs764959531	snp	A/C	1.64885e-05	0.00287123	synonymous-codon	TFG	GRCh38.p7	3:100728780	GAACTGATAGAACTT[A/C]GAAATAAAGTGAATC	10342
rs764971958	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100718900	GTCCGTTAGATTCTG[C/T]TAGTAGAGTGGAGGG	10342
rs765007275	snp	A/G			upstream-variant-2KB	TFG	GRCh38.p7	3:100708870	TTTGAACAGGTAAGG[A/G]AGAAGGGAAGAGTAC	10342
rs765015665	in-del	-/G			intron-variant	TFG	GRCh38.p7	3:100720831	AGGCAGAACTCTTAA[-/G]GGACAAGATAGAAAA	10342
rs765052576	snp	A/G	1.64789e-05	0.0028704	missense	TFG	GRCh38.p7	3:100744840	GTTTTCAGGTCAGAT[A/G]TACCAACAGTACCAG	10342
rs765179117	snp	A/T			downstream-variant-500B	TFG, ABI3BP	GRCh38.p7	3:100748995	TTTTAATTTAGTCAC[A/T]AACATTATGTGAAAA	10342
rs765206014	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100727473	GATGTCCTTTTCTAA[C/T]TAGGTGCTTCAGGAG	10342
rs765212854	snp	A/T			intron-variant	TFG	GRCh38.p7	3:100744992	ATACTCATTAAACTT[A/T]AAGTTCTTAATTCCT	10342
rs765257165	snp	C/G			intron-variant	TFG	GRCh38.p7	3:100739509	AAGAACGCTAAAAAT[C/G]ATCAGAGATCGGGAG	10342
rs765295824	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100717716	TAGAAACACTACTTA[C/T]TTTTGTGTACTTATT	10342
rs765359621	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100747287	GTTTCTTTCATGAGT[A/G]AATTTTGAACCCAGG	10342
rs765413318	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100735428	TTCCTTTTATAAGCC[C/T]ATGCTATAAGCTCTT	10342
rs765480156	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100736983	GTCAGTGGTGACCCT[C/T]GGAGGGGAGGATAGT	10342
rs765514283	snp	C/G			intron-variant	TFG	GRCh38.p7	3:100744118	TCATAGGTAATAAGT[C/G]TCTAAAGGGTTTCTT	10342
rs765636091	snp	A/G	1.64969e-05	0.00287196	synonymous-codon	TFG	GRCh38.p7	3:100736610	AGAAGATCGTTCAGG[A/G]ACACCCGACAGCATT	10342
rs765671948	in-del	-/AA			intron-variant	TFG	GRCh38.p7	3:100741585	AAGAAATGGAATTTT[-/AA]AAAATAAATGTAGTA	10342
rs765751527	in-del	-/A	5.00146e-05	0.00500048	intron-variant	TFG	GRCh38.p7	3:100728869	AAATGGTAAACCCTG[-/A]ATCCATTGTATTCTG	10342
rs765753301	snp	A/T			intron-variant	TFG	GRCh38.p7	3:100712464	GTAGTAGTTTGTAGG[A/T]TACCTTGAAAAGTCT	10342
rs765777802	snp	A/C/G	0.000103662	0.0071987	utr-variant-5-prime	TFG	GRCh38.p7	3:100713662	TCTCTAGAGTTGTAT[A/C/G]TATAGAACATCCTGG	10342
rs765831498	snp	A/C			intron-variant	TFG	GRCh38.p7	3:100744476	ATTTGTCCCTTTTCT[A/C]ATTTTTATTTACTGA	10342
rs765882997	snp	G/T			intron-variant	TFG	GRCh38.p7	3:100735196	TTTTGGCAATCATCA[G/T]TCTCTCTTGCATTAC	10342
rs765888491	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100742702	AGACTCTACACAGAA[C/T]AGTAACCCCAACTGG	10342
rs765918854	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100720938	GTTTAGCATTAATTT[C/T]ATTTTTTTTTAATTT	10342
rs766030746	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100727772	ATACTGTTTCTGGAA[A/G]TAACTGCTTTGAAGG	10342
rs766049461	snp	C/T	1.65869e-05	0.00287979	missense	TFG	GRCh38.p7	3:100748485	ATGCGCGTAACCGTC[C/T]TCCCTTTGGTCAGGG	10342
rs766049936	in-del	-/TACACCC	3.40669e-05	0.00412702	intron-variant	TFG	GRCh38.p7	3:100732694	GGTTTCCAACTCCTT[-/TACACCC]TACACCCTTCGTTTC	10342
rs766085001	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100734253	TCCTTCTTTCTCCCT[A/G]TGGTGTATAGCAGCT	10342
rs766088240	snp	G/T			utr-variant-3-prime	TFG	GRCh38.p7	3:100748705	ACACAAAGACCAAAA[G/T]GAAAGTTTTTTCCTC	10342
rs766093952	snp	C/T			splice-donor-variant, upstream-variant-2KB, utr-variant-5-prime	TFG	GRCh38.p7	3:100709433	CGCATGCGTCCTGGG[C/T]ATGTCCACGCGCAAT	10342
rs766103728	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100740686	ACATGTGCAGAAGCC[A/G]TTGAGGGTCATGATA	10342
rs766158298	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100720093	ATGAATTTACTATTT[C/T]ATTCATTGTATTTTA	10342
rs766315965	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100716568	TTCAGTAGTGGCATC[A/G]CTGAATTGTGTGTTA	10342
rs766331035	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100729024	CTAAACTTTGCTGTT[C/T]ATCAGAATTACTAGG	10342
rs766374092	snp	A/C	1.66032e-05	0.0028812	missense	TFG	GRCh38.p7	3:100748181	ACTGGACCTCAACAA[A/C]CTCAGCAGTTCCAGG	10342
rs766429583	snp	G/T			upstream-variant-2KB	TFG	GRCh38.p7	3:100708030	CAGAATTTACTCCAG[G/T]TCCTTTAGGAGTATC	10342
rs766430750	snp	C/T	1.72225e-05	0.00293444	intron-variant	TFG	GRCh38.p7	3:100744980	TTTTTTGTTTCTATA[C/T]TCATTAAACTTTAAG	10342
rs766481768	snp	A/T			intron-variant	TFG	GRCh38.p7	3:100741584	GAAGAAATGGAATTT[A/T]AAAAAATAAATGTAG	10342
rs766483726	snp	A/G	5.06333e-05	0.00503131	synonymous-codon	TFG	GRCh38.p7	3:100713862	AACAATAAAGTATAA[A/G]GATGAAGGTAAGAGT	10342
rs766495385	snp	A/T	0.00012093	0.00777498	intron-variant	TFG	GRCh38.p7	3:100713912	AAAGTCTTTTTAAAA[A/T]AAAAAAAAAAAAGAC	10342
rs766538439	snp	G/T			intron-variant	TFG	GRCh38.p7	3:100724688	AACATAGATAGAAAA[G/T]ATTAAGTAATATTTA	10342
rs766593431	in-del	-/G	1.64814e-05	0.00287061	intron-variant	TFG	GRCh38.p7	3:100744825	TGTGTGTGTGTGTGT[-/G]TTTTCAGGTCAGATG	10342
rs766716590	snp	A/T			intron-variant	TFG	GRCh38.p7	3:100744639	AGTTCTCTGCAGTTA[A/T]TCCACAGCAGAGGAA	10342
rs766735962	snp	C/T	1.65201e-05	0.00287398	synonymous-codon	TFG	GRCh38.p7	3:100732623	AAACCAAGATGAAAT[C/T]AATAAAAATGTTATG	10342
rs766739527	in-del	-/AGAAC			intron-variant	TFG	GRCh38.p7	3:100723402	GAAAGCTCAATAGAT[-/AGAAC]AGAATACTAATCACA	10342
rs766781580	snp	A/T			intron-variant	TFG	GRCh38.p7	3:100733099	TCTTGTTAAATTGCT[A/T]GAGTATACAGTGGGT	10342
rs766837297	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100714086	TTAAGTATTGTATGT[A/G]TTATTTTGCCCATTT	10342
rs766899074	snp	C/T	1.64963e-05	0.00287192	missense	TFG	GRCh38.p7	3:100732574	AGTCTACTCAGGTTA[C/T]GGCAGCAAGTATGTC	10342
rs767003179	in-del	-/T			intron-variant	TFG	GRCh38.p7	3:100746293	CCCCATTCCCAGAGA[-/T]TTTTGAATTTCATTT	10342
rs767064551	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100742207	GGGTTTAAAGTAAGT[A/G]CCGTAAATCCTCACT	10342
rs767096549	in-del	-/T			intron-variant	TFG	GRCh38.p7	3:100736557	GGATACTAAACTGAC[-/T]TTTTTTTTGACTATC	10342
rs767146719	snp	C/G			intron-variant	TFG	GRCh38.p7	3:100729211	CATGAACCCTTTTTA[C/G]TATAATAGATAAGTA	10342
rs767193344	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100745911	ACCATGTGGCCCACA[A/G]AGCCTAAACTATTTA	10342
rs767236753	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100730095	ATGAAAAAGTTAGAC[A/G]ATTTTTCCAGAAGAA	10342
rs767236849	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100716747	ACTGGGGTGAACCTT[A/G]TTGTGGTCTTCATTT	10342
rs767238036	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100740996	ACAAGGCATTACTTA[C/T]GTGTTTGTGGTGATT	10342
rs767292808	snp	C/G			intron-variant, upstream-variant-2KB	TFG	GRCh38.p7	3:100710843	AGTTAATACCAGTCT[C/G]TACTTTGGAAGAGAA	10342
rs767297003	snp	A/G	3.32347e-05	0.00407631	missense	TFG	GRCh38.p7	3:100748221	AGCAACCAACTTCCC[A/G]GGCACCAGCTCCTGC	10342
rs767308241	snp	A/G	1.85706e-05	0.00304712	intron-variant	TFG	GRCh38.p7	3:100719948	TTAAAAAATTAAAAA[A/G]CAACCTTTTTTTTTT	10342
rs767327465	in-del	-/T	6.67523e-05	0.00577683	intron-variant	TFG	GRCh38.p7	3:100744958	TGAAAGGGAGTTGGC[-/T]TCATGGTTTTTTGTT	10342
rs767431238	snp	A/T	1.66167e-05	0.00288237	intron-variant	TFG	GRCh38.p7	3:100720076	GAGTAGTAAACTTTC[A/T]AATGAATTTACTATT	10342
rs767657694	snp	C/G			intron-variant	TFG	GRCh38.p7	3:100714172	ATTGAATGTGATGTT[C/G]CTATAGTTACTATAA	10342
rs767723297	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100745769	TCAGTAAAGTATAGC[C/T]CACAGGCCAAATCTG	10342
rs767814550	in-del	-/T			intron-variant	TFG	GRCh38.p7	3:100738718	CATACAGTATGAAAA[-/T]TGTACAATTAATATG	10342
rs767892218	snp	A/G	1.67192e-05	0.00289125	missense	TFG	GRCh38.p7	3:100713845	CTGAGTAATGATGAA[A/G]TAACAATAAAGTATA	10342
rs767951153	snp	C/G			intron-variant	TFG	GRCh38.p7	3:100720246	TTTAAGAAAATGATA[C/G]AAGTTTAATTCAGTA	10342
rs768204691	in-del	-/A			intron-variant	TFG	GRCh38.p7	3:100741169	TACTCCTACTTATTT[-/A]AAAAAAAAACAAAGC	10342
rs768205562	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100713410	AAAATCTAAATGGTC[A/G]TGTCAGATGAACAGT	10342
rs768236185	snp	A/G	1.67189e-05	0.00289122	synonymous-codon	TFG	GRCh38.p7	3:100732665	CTTAACAGATGATCA[A/G]GTTTCAGGTAAGTTG	10342
rs768404956	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100745214	TTACTAACATTATCA[A/G]TTTATCTCTTAGGCG	10342
rs768456880	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100734783	AGGTCAGACTTTTAA[A/G]TTTTGATTTAAATGT	10342
rs768550035	snp	C/G			upstream-variant-2KB	TFG	GRCh38.p7	3:100708792	CCTCTTAGTAATTTT[C/G]CATCCACTGACCGAC	10342
rs768551069	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100728927	GTTTTAAAAAACTCT[C/T]TTTAAGTAGGAGAAG	10342
rs768565054	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100732855	ACTAGATTAAGATGT[A/G]GATGATTTCCAGCAC	10342
rs768565255	in-del	-/T	0.0112403	0.0741201	intron-variant	TFG	GRCh38.p7	3:100719953	AATTAAAAAACAACC[-/T]TTTTTTTTTTTTAAA	10342
rs768680846	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100728122	TACAGGTGTGAGCCA[C/T]CATGCCTGGCCCTGC	10342
rs768710296	snp	A/T			intron-variant	TFG	GRCh38.p7	3:100741975	TGACACAATTTTCAG[A/T]ACCTACTCTTGTCAT	10342
rs768746409	snp	A/G	0.000248495	0.0111439	missense	TFG	GRCh38.p7	3:100728844	CAGGACCTTCCACCA[A/G]TATTCCTGAAAATGG	10342
rs768778239	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100716417	TTGTGTATATATACC[A/G]TATTTTCTTTATCAG	10342
rs768945051	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100729710	CATATAAAGGGCTTA[A/G]CATGAGATAATTTTT	10342
rs768966865	snp	A/T			intron-variant	TFG	GRCh38.p7	3:100717502	CTTTGAGTAATTTTG[A/T]CATTTTAACAATATT	10342
rs769041703	snp	C/T	3.29723e-05	0.00406018	synonymous-codon	TFG	GRCh38.p7	3:100713784	TGAAGATATTACTTA[C/T]GATGAATTAGTGCTA	10342
rs769119645	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100742569	CCACACACACACCCA[C/T]AGTCGTTCAGACTGA	10342
rs769126767	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100724384	ACTTTAAAAATTTAT[A/G]TATACCATGAATTCC	10342
rs769197543	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100718419	TTTTACAATGTAAAA[A/G]CCATTTTTCATTCAC	10342
rs769228702	in-del	-/TTGA			intron-variant	TFG	GRCh38.p7	3:100717002	GTTCTCTTTTCACTC[-/TTGA]TTGTTTCCTTTGCTG	10342
rs769256046	snp	A/G	0.000915912	0.0213803	intron-variant	TFG	GRCh38.p7	3:100713900	AAGCTATTTTTTAAA[A/G]TCTTTTTAAAAAAAA	10342
rs769283291	snp	A/G	0.000134971	0.00821385	missense	TFG	GRCh38.p7	3:100748155	CCTTTTCAGCAAGCT[A/G]TAGTCAGCAGACTGG	10342
rs769287647	snp	G/T			upstream-variant-2KB	TFG	GRCh38.p7	3:100707696	CATCCCAAACCATCT[G/T]AATGACATCATAATA	10342
rs769347583	snp	G/T			intron-variant	TFG	GRCh38.p7	3:100714612	TGTCCATATAATTCT[G/T]GTTTCTTTTAGCTTA	10342
rs769373702	snp	A/G	4.28018e-05	0.00462591	intron-variant	TFG	GRCh38.p7	3:100713897	TTAAAGCTATTTTTT[A/G]AAGTCTTTTTAAAAA	10342
rs769516147	in-del	-/TTTT			intron-variant	TFG	GRCh38.p7	3:100737143	TTTAGTTGTAGTGGG[-/TTTT]TTTTGTTAAGATTAG	10342
rs769693454	snp	G/T			intron-variant	TFG	GRCh38.p7	3:100722052	GCTACTTGAGAGGCT[G/T]AGGCAGGAGAATTGC	10342
rs769746368	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100719372	ACAGTTGGTATGCCA[A/G]TTATAGCATTCTTTA	10342
rs769864892	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100723154	AAATACTGGGCAATA[A/G]TATGTAAGAAAGGAA	10342
rs769868796	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100719422	TTCACGGTCATAAAT[A/G]CACACTGTTTTGAAT	10342
rs769879097	snp	A/T	1.65162e-05	0.00287365	missense	TFG	GRCh38.p7	3:100748469	AGTGGGCCTAATCCT[A/T]ATGCGCGTAACCGTC	10342
rs769885874	in-del	-/AAAGAC	0.000260256	0.0114044	intron-variant	TFG	GRCh38.p7	3:100713922	TAAAAAAAAAAAAAA[-/AAAGAC]AGAGCCTCTGTTGCC	10342
rs769902536	in-del	-/T			intron-variant	TFG	GRCh38.p7	3:100723832	TAGGGAGAAATACAG[-/T]TTTTTTTTTTTTCGA	10342
rs769930436	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100730816	AGCAAGTAGTAGGAC[A/G]TATAGTATGTTTCCT	10342
rs770021533	snp	C/G			upstream-variant-2KB	TFG	GRCh38.p7	3:100707837	TGCAGTACTCCACTC[C/G]CTTATCCCTGCAAAC	10342
rs770053266	snp	C/T	1.65247e-05	0.00287438	missense	TFG	GRCh38.p7	3:100728834	CCTGGAGAACCAGGA[C/T]CTTCCACCAATATTC	10342
rs770072237	snp	C/G			intron-variant	TFG	GRCh38.p7	3:100718463	CACAGGGATTTTGTC[C/G]GTTGGTCACAGTTCA	10342
rs770108643	snp	C/T			upstream-variant-2KB	TFG	GRCh38.p7	3:100708498	GGTAGGGTCTAAATG[C/T]TTTATTTATCAGCTT	10342
rs770158032	in-del	-/TTT			intron-variant	TFG	GRCh38.p7	3:100718552	TTGTATTTCATGGTT[-/TTT]TTTTTTTTTTTTTTT	10342
rs770184325	snp	A/C	1.65636e-05	0.00287776	intron-variant	TFG	GRCh38.p7	3:100736749	ACACATGTTTGGGAA[A/C]GTACATGTGTAGAAG	10342
rs770200478	in-del	-/TTTTT			intron-variant	TFG	GRCh38.p7	3:100718550	CTTTGTATTTCATGG[-/TTTTT]TTTTTTTTTTTTTTT	10342
rs770221247	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100725354	ATCTAACATGGCAAG[A/G]TTGTTTTGGATGAAA	10342
rs770280574	snp	A/G			missense	TFG	GRCh38.p7	3:100748269	AACAACTGCCTGCTC[A/G]GCCGCCACAGCAGTA	10342
rs770376829	snp	C/G	4.94442e-05	0.00497188	missense	TFG	GRCh38.p7	3:100744892	CAGCAGCCGCAGGCT[C/G]CACCTCAGCAGCCTC	10342
rs770383052	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100725064	ACCTGCCACCACGCC[C/T]GGCTAATTTGTTTTT	10342
rs770392242	snp	A/T			intron-variant	TFG	GRCh38.p7	3:100737610	TCTAACTATTTGTTT[A/T]ACGGGTCAGATAGTG	10342
rs770405717	snp	C/G			intron-variant	TFG	GRCh38.p7	3:100734121	TGTGGTTTTTGAACT[C/G]TTTTGTGATAGTTTT	10342
rs770439532	snp	C/G	8.24491e-05	0.0064201	missense	TFG	GRCh38.p7	3:100736696	ATACAGGAGCTCAGA[C/G]TCAAGCAGGTCAGAT	10342
rs770678209	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100723346	GAAAACAAGGGTACC[C/T]GTTCAGTTCAGTAGA	10342
rs770811877	snp	A/G	3.30748e-05	0.00406649	synonymous-codon	TFG	GRCh38.p7	3:100732524	TACTGTGGATGGTAG[A/G]GAAGAAAAGTCTGCT	10342
rs770911064	snp	A/T			intron-variant, upstream-variant-2KB	TFG	GRCh38.p7	3:100710790	ACAAGATGGGAGAAG[A/T]GCTTGTCGTAGGGCT	10342
rs771095995	snp	C/T	1.64901e-05	0.00287137	missense	TFG	GRCh38.p7	3:100748445	GGAAGTACCATGACC[C/T]CTCCTCCAAGTGGGC	10342
rs771190550	snp	A/G			upstream-variant-2KB	TFG	GRCh38.p7	3:100708649	AAGGCAGTGTAGTGA[A/G]AATCCCTCACCCTTG	10342
rs771218685	snp	A/G	0.000249064	0.0111566	synonymous-codon	TFG	GRCh38.p7	3:100728722	TTCAGTTAATGGCCA[A/G]CCAAGACCCCTTGAA	10342
rs771223027	snp	A/G	1.65446e-05	0.00287612	synonymous-codon	TFG	GRCh38.p7	3:100720021	TGACCTTTCCTTTGC[A/G]ATTCAGTGCAGTAGG	10342
rs771271513	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100727247	CCAGTTTCTGGCTGC[C/T]AGGAGCTGTTTTTCT	10342
rs771274688	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100734539	CGCTTTTAATTCTTA[C/T]CCATTCTAATTTTAT	10342
rs771311509	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100738296	AGATGTCAGCTGAAA[C/T]GGACAAAAGCAGAGT	10342
rs771329796	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100733416	AGCTCTAGAATTTCC[A/G]TTGGGTTTTTATAGT	10342
rs771357762	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100714824	GTATGCAGTGTTCCC[A/G]GACTCATTTGTTGAC	10342
rs771454367	snp	C/G			intron-variant	TFG	GRCh38.p7	3:100746576	TGTCCTTCACCTAAA[C/G]TTATTTATTATTTTG	10342
rs771511466	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100745228	AGTTTATCTCTTAGG[C/T]GACTTAGTGCAAGTT	10342
rs771619425	snp	C/T	1.65091e-05	0.00287303	synonymous-codon	TFG	GRCh38.p7	3:100736586	TCCAGGGCCACCCAG[C/T]GCTCCTGCAGAAGAT	10342
rs771637543	snp	C/G			intron-variant	TFG	GRCh38.p7	3:100724200	ACAGTTACAAAAGGA[C/G]AAACCTCAAATAACT	10342
rs771737493	in-del	-/T			intron-variant	TFG	GRCh38.p7	3:100719003	CAGGAAGTTTTCTTC[-/T]TTTACATACATACTT	10342
rs771795676	snp	A/G	1.64879e-05	0.00287118	missense	TFG	GRCh38.p7	3:100736683	CAGCAGCCACCATAT[A/G]CAGGAGCTCAGACTC	10342
rs771836549	snp	C/T	5.03529e-05	0.00501736	synonymous-codon	TFG	GRCh38.p7	3:100713691	GGAGTCCACCATGAA[C/T]GGACAGTTGGATCTA	10342
rs771896098	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100722449	AAGGAGAGAATGGGA[A/G]AGTGGAAATACATTG	10342
rs771928028	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100745154	CTTACAGTAGATGAT[C/T]CTGCAGTAACTTGTA	10342
rs771983068	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100739499	TGGTAAGGAGAAGAA[C/T]GCTAAAAATCATCAG	10342
rs772089337	in-del	-/TACC			intron-variant	TFG	GRCh38.p7	3:100743363	ATTTCTGTACCTACT[-/TACC]TTTTTATTTTAGATT	10342
rs772205995	in-del	-/TA	1.73791e-05	0.00294775	utr-variant-5-prime	TFG	GRCh38.p7	3:100713646	ACTTTTATCAGTCTT[-/TA]TCTCTAGAGTTGTAT	10342
rs772310607	in-del	-/C	1.8332e-05	0.00302748	intron-variant	TFG	GRCh38.p7	3:100719952	AAAATTAAAAAACAA[-/C]CTTTTTTTTTTTTAA	10342
rs772530102	snp	C/T	1.72305e-05	0.00293513	intron-variant	TFG	GRCh38.p7	3:100732702	AACTCCTTTACACCC[C/T]TCGTTTCCTTCATCT	10342
rs772577239	snp	A/G	1.65545e-05	0.00287697	synonymous-codon	TFG	GRCh38.p7	3:100748291	ACAGCAGTACCAGGC[A/G]AGCAATTATCCTGCA	10342
rs772577601	snp	A/T	0.474376	0.110251	intron-variant	TFG	GRCh38.p7	3:100713909	TTTAAAGTCTTTTTA[A/T]AAAAAAAAAAAAAAA	10342
rs772614502	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100735133	ATTTATCTACATAGA[C/T]ATAAATTTAAGTAAA	10342
rs772617560	snp	G/T			intron-variant	TFG	GRCh38.p7	3:100745440	CATAAAAATAAAATC[G/T]TATAAAATGTAATTC	10342
rs772624258	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100716112	TGAAATTATATAATA[C/T]GTTATTGTTAACTGT	10342
rs772701898	snp	A/G	3.31076e-05	0.0040685	missense	TFG	GRCh38.p7	3:100720002	TAACAATTTTTGATA[A/G]TTCTGACCTTTCCTT	10342
rs772982883	in-del	-/TA			intron-variant	TFG	GRCh38.p7	3:100730795	AGTATCTCCAGCAGC[-/TA]ATGGAGCAAGTAGTA	10342
rs773054020	snp	C/G			intron-variant	TFG	GRCh38.p7	3:100720723	AGTATTTCCCGAGGG[C/G]TACTTAAAGATTAAA	10342
rs773056124	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100734016	AGTCTGAGGTTGGAC[A/G]GGCAGTTTCTGGGCA	10342
rs773089017	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100723171	ATGTAAGAAAGGAAG[A/G]GATGATAGGAATAAA	10342
rs773141921	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100722099	GAGGTTGCAGTGAGT[C/T]GAGATCGCGCCACTG	10342
rs773147150	snp	G/T			intron-variant	TFG	GRCh38.p7	3:100711718	TCCTTTTACATTATT[G/T]CTGGTTTACACTTCT	10342
rs773234775	snp	C/G	1.84337e-05	0.00303587	utr-variant-3-prime	TFG	GRCh38.p7	3:100748579	TAGCTATTGGCCTCC[C/G]AAAAGACTCCAGTAC	10342
rs773343687	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100717768	AATTCATTTATTGGT[C/T]CTAAGGGTTTTGGTA	10342
rs773349605	snp	C/T			upstream-variant-2KB	TFG	GRCh38.p7	3:100708005	AACGTAGCTTCTCAC[C/T]CTGAAACACCAGAAT	10342
rs773391088	snp	C/T	1.66994e-05	0.00288953	intron-variant	TFG	GRCh38.p7	3:100744960	GAAAGGGAGTTGGCT[C/T]ATGGTTTTTTGTTTC	10342
rs773582951	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100725438	GGGAGATTTAATTAT[A/G]TCTATGCTGTTTCAT	10342
rs773638091	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100738210	TTAAGCCTTTTCTCA[A/G]CCAACTTTAATTAAC	10342
rs773643503	snp	A/T	0.024177	0.107257	intron-variant	TFG	GRCh38.p7	3:100713910	TTAAAGTCTTTTTAA[A/T]AAAAAAAAAAAAAAG	10342
rs773643790	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100727235	TACTGTACCAGACCA[A/G]TTTCTGGCTGCTAGG	10342
rs773684378	in-del	-/CAGAGAGATTACCTTAAAAGTAGC			intron-variant	TFG	GRCh38.p7	3:100722607	GAAAATGTCTTAAGA[-/CAGAGAGATTACCTTAAAAGTAGC]CAGAGAGAATAAGAC	10342
rs773721621	in-del	-/A			intron-variant, upstream-variant-2KB	TFG	GRCh38.p7	3:100710695	ATTCCCAGTGCTGAG[-/A]AAAGTGTACCTGGTA	10342
rs773749922	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100734185	TTTTTAATTTTTTTT[C/T]AACATTAATGACTTC	10342
rs773769795	snp	C/T	1.65529e-05	0.00287683	synonymous-codon	TFG	GRCh38.p7	3:100720003	AACAATTTTTGATAG[C/T]TCTGACCTTTCCTTT	10342
rs773773830	in-del	-/GTG	2.86668e-05	0.00378584	intron-variant	TFG	GRCh38.p7	3:100744809	ATGCCTTTTTTCCTT[-/GTG]TGTGTGTGTGTGTGT	10342
rs773786874	snp	C/G	1.64947e-05	0.00287177	missense	TFG	GRCh38.p7	3:100732560	TTCTTCTGGAAAACA[C/G]TCTACTCAGGTTATG	10342
rs773873058	snp	C/G			intron-variant	TFG	GRCh38.p7	3:100735023	GAATGAATATTAACT[C/G]TAATAAATTACATAT	10342
rs774086902	snp	C/T	1.67626e-05	0.002895	missense	TFG	GRCh38.p7	3:100732669	ACAGATGATCAGGTT[C/T]CAGGTAAGTTGGTTT	10342
rs774100103	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100742181	CAGTCCCATTTGGAC[C/T]TGAATGAGGTGGGTT	10342
rs774145581	snp	A/G			intron-variant, upstream-variant-2KB	TFG	GRCh38.p7	3:100710809	TGTCGTAGGGCTCCT[A/G]CTGGCAGTTCTAGGA	10342
rs774200693	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100723358	ACCTGTTCAGTTCAG[C/T]AGAAAGTGGTGGCGG	10342
rs774298210	snp	A/G	0.00046213	0.0151938	synonymous-codon	TFG	GRCh38.p7	3:100748324	AACTTACACTGCCCA[A/G]ACTTCTCAGCCTACT	10342
rs774357786	snp	C/T	1.65762e-05	0.00287886	missense	TFG	GRCh38.p7	3:100728847	GACCTTCCACCAATA[C/T]TCCTGAAAATGGTAA	10342
rs774509063	snp	G/T			intron-variant	TFG	GRCh38.p7	3:100728186	CTATTTTAGTTAGCT[G/T]TTTTTTTTCAAGACA	10342
rs774542851	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100738356	TCAAGCGAACTAAAG[A/G]TTTGTTTTTAAATAA	10342
rs774731833	snp	C/G			intron-variant	TFG	GRCh38.p7	3:100714827	TGCAGTGTTCCCAGA[C/G]TCATTTGTTGACAAA	10342
rs774780984	in-del	-/CAGCAGCCGCAGGCTCCACCT	1.64836e-05	0.0028708	cds-indel	TFG	GRCh38.p7	3:100744877	GCCGGCTATGGTGCA[-/CAGCAGCCGCAGGCTCCACCT]CAGCAGCCTCAACAG	10342
rs774787553	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100746631	TATACACACACACAC[A/G]TGATAGAAGCATTGC	10342
rs774790215	snp	C/T	1.65247e-05	0.00287438	intron-variant	TFG	GRCh38.p7	3:100744937	CAGTATTCAGGTGAG[C/T]AGGTGTTGAAAGGGA	10342
rs774808090	snp	A/G	3.29701e-05	0.00406005	missense	TFG	GRCh38.p7	3:100713753	GGGAGGATATTCGGC[A/G]AATTCCTATTCATAA	10342
rs774838217	snp	C/T	1.65384e-05	0.00287557	synonymous-codon	TFG	GRCh38.p7	3:100713817	GATGCAACGAGTTTT[C/T]AGAGGAAAACTTCTG	10342
rs774865395	snp	C/G			intron-variant	TFG	GRCh38.p7	3:100727296	AAACAGTAATACCAA[C/G]TGAAAACCAATAATT	10342
rs774867242	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100723605	ACAGAATAGACTTAT[A/G]TAAAAACTTGAGTAG	10342
rs774895555	in-del	-/TT			intron-variant	TFG	GRCh38.p7	3:100717281	TGGTCTGTGGGTCCG[-/TT]TTTGTGCCAGTCCAT	10342
rs775034252	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100719393	GCATTCTTTATCCCT[A/G]AGATCTGGGGGATTT	10342
rs775088744	in-del	-/T			intron-variant	TFG	GRCh38.p7	3:100719756	TCATGTGGATATGTG[-/T]TAAATACCTTGCCAT	10342
rs775112338	snp	A/T			intron-variant	TFG	GRCh38.p7	3:100731421	ATGATTTTAAATTTA[A/T]CCTGCTCATAATATT	10342
rs775165387	snp	G/T			intron-variant	TFG	GRCh38.p7	3:100743820	TTTTTTTTTTCTCAC[G/T]TCAGCAGTAAGTATC	10342
rs775248788	snp	A/T			intron-variant	TFG	GRCh38.p7	3:100712035	TGCATTAAGATAAGC[A/T]TGGCATCCCTAGAGT	10342
rs775281979	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100742238	TAACATTGTTGATAG[A/G]TTCTTGGAAATTGTA	10342
rs775354552	snp	C/T	4.94907e-05	0.00497422	missense	TFG	GRCh38.p7	3:100732550	CTGCTTCTGATTCTT[C/T]TGGAAAACAGTCTAC	10342
rs775457145	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100718715	GGCACACACCACCAC[A/G]CTCGGCTGATTTTTG	10342
rs775485992	snp	A/G	1.65581e-05	0.00287728	synonymous-codon	TFG	GRCh38.p7	3:100720054	ACTGAAACTGACATT[A/G]TTTGGTGAGTAGTAA	10342
rs775549986	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100732773	ACTTGGATATGGTGA[A/G]GTGCACAAATCTTAA	10342
rs775608477	snp	C/T	3.29951e-05	0.00406159	missense	TFG	GRCh38.p7	3:100728753	TCAAGTCAGGTGAAA[C/T]ATCTCCGTCGAGAAC	10342
rs775617560	in-del	-/C	0.0066556	0.0573019	intron-variant	TFG	GRCh38.p7	3:100713901	GCTATTTTTTAAAGT[-/C]CTTTTTAAAAAAAAA	10342
rs775646299	in-del	-/TT	0.00664845	0.0572715	intron-variant	TFG	GRCh38.p7	3:100719954	AATTAAAAAACAACC[-/TT]TTTTTTTTTTAAATT	10342
rs775654340	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100739500	GGTAAGGAGAAGAAC[A/G]CTAAAAATCATCAGA	10342
rs775673360	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100727402	AGCTTATAATTGGTG[A/G]TTTGATTTTGAAACA	10342
rs775802926	snp	A/G			utr-variant-3-prime	TFG	GRCh38.p7	3:100748573	AGCTGCTAGCTATTG[A/G]CCTCCCAAAAGACTC	10342
rs775856048	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100746795	GCCAGGATGAAAAGG[C/T]ACTTTTCTTTTTTCT	10342
rs775895691	snp	A/G	3.29663e-05	0.00405981	synonymous-codon	TFG	GRCh38.p7	3:100744894	GCAGCCGCAGGCTCC[A/G]CCTCAGCAGCCTCAA	10342
rs775947594	snp	G/T			intron-variant	TFG	GRCh38.p7	3:100717243	TCTCTTGGTCAATGG[G/T]TCTGTTTTTATGTCA	10342
rs775968930	snp	C/T	1.66643e-05	0.0028865	intron-variant	TFG	GRCh38.p7	3:100744788	TTTCTCTTTGCCACA[C/T]TAAACATGCCTTTTT	10342
rs776000679	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100716137	AACTGTAGTCATCCT[A/G]TAGTGCTATAGAACA	10342
rs776008045	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100712243	AGGGCATTAATATAT[A/G]ATATTCATATAATAG	10342
rs776038175	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100742618	AGTAACCTAACATAC[A/G]CATCTTTGGGATGTG	10342
rs776068618	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100713457	TAATAGTAGACGTAA[A/G]ATAAAAGCTTATTTT	10342
rs776123523	snp	A/T			intron-variant	TFG	GRCh38.p7	3:100725313	TACCTATTATAATTA[A/T]ATACAACAAAAGATA	10342
rs776179502	snp	A/G	1.7342e-05	0.0029446	utr-variant-5-prime	TFG	GRCh38.p7	3:100713652	TATCAGTCTTTCTCT[A/G]GAGTTGTATATATAG	10342
rs776254365	snp	C/G			intron-variant	TFG	GRCh38.p7	3:100744200	TCAAGAACACATCAC[C/G]GTTGTTAAAAAGGTC	10342
rs776282551	in-del	-/ATTTAAG			intron-variant	TFG	GRCh38.p7	3:100728366	TTAAATTTAATAAAT[-/ATTTAAG]AACAGCATGAAATAA	10342
rs776301041	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100732867	TGTAGATGATTTCCA[A/G]CACTTCAGAAAGCTT	10342
rs776597646	snp	C/T			upstream-variant-2KB	TFG	GRCh38.p7	3:100708804	TTTCCATCCACTGAC[C/T]GACTTCCACCCCTTG	10342
rs776620173	snp	G/T	0.000280906	0.011848	missense	TFG	GRCh38.p7	3:100748304	GCGAGCAATTATCCT[G/T]CACAAACTTACACTG	10342
rs776659928	snp	A/G	3.306e-05	0.00406558	missense	TFG	GRCh38.p7	3:100732526	CTGTGGATGGTAGGG[A/G]AGAAAAGTCTGCTTC	10342
rs776693527	in-del	-/A	0.000219317	0.0104695	intron-variant	TFG	GRCh38.p7	3:100719966	ACCTTTTTTTTTTTT[-/A]AATTCCAGATGGAGA	10342
rs776703898	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100741988	AGAACCTACTCTTGT[C/T]ATTAAGCAATGCATG	10342
rs776763646	snp	G/T			intron-variant	TFG	GRCh38.p7	3:100717537	CTTATATAAGCATGG[G/T]ATGTCATTACATATG	10342
rs776764490	snp	G/T	1.66015e-05	0.00288105	missense	TFG	GRCh38.p7	3:100748189	TCAACAACCTCAGCA[G/T]TTCCAGGGATATGGC	10342
rs776784973	snp	A/T			intron-variant	TFG	GRCh38.p7	3:100728935	AAACTCTTTTTAAGT[A/T]GGAGAAGGATGGCAT	10342
rs776795702	in-del	-/AA			utr-variant-3-prime	TFG	GRCh38.p7	3:100748777	TACTCTTACATGTAT[-/AA]AAAGTGATTGACTTG	10342
rs776819497	snp	A/G	3.24649e-05	0.00402882	intron-variant	TFG	GRCh38.p7	3:100713920	TTTAAAAAAAAAAAA[A/G]AAAAGACAGAGCCTC	10342
rs776996464	in-del	-/TA			intron-variant	TFG	GRCh38.p7	3:100746167	ATCAGTGTTACAAAC[-/TA]TGTTATTTATAGAAA	10342
rs777000435	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100735319	GAGCAGAAGATAGAG[A/G]TTTGCCCTTAGAGAA	10342
rs777058539	snp	C/G			intron-variant	TFG	GRCh38.p7	3:100738001	GAATTGAAGTGGGTG[C/G]TCTAGGCTGCAGTGA	10342
rs777065922	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100747677	AAGATTGTGAAAATG[A/G]TACTTTTTATTTATT	10342
rs777093212	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100729426	TTGTGTTAAGATAAA[A/G]CAAAATGTGTCAACA	10342
rs777123497	in-del	-/T			intron-variant	TFG	GRCh38.p7	3:100713903	TATTTTTTAAAGTCT[-/T]TTTTAAAAAAAAAAA	10342
rs777143620	snp	C/T	1.65015e-05	0.00287237	missense	TFG	GRCh38.p7	3:100736602	GCTCCTGCAGAAGAT[C/T]GTTCAGGAACACCCG	10342
rs777211186	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100715594	GTCTAAGAATACCCA[A/G]AACAAATTTTTGAGA	10342
rs777228595	in-del	-/G			utr-variant-5-prime, upstream-variant-2KB	TFG	GRCh38.p7	3:100709291	AAACCGGAAGTGCGT[-/G]GTCACGCCCCGCGCA	10342
rs777434458	snp	A/G	3.29761e-05	0.00406041	synonymous-codon	TFG	GRCh38.p7	3:100736685	GCAGCCACCATATAC[A/G]GGAGCTCAGACTCAA	10342
rs777437297	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100716866	AATGTCTGTTCAGAT[C/T]ATTTGCCGATTTTAA	10342
rs777523583	in-del	-/CTACT			intron-variant	TFG	GRCh38.p7	3:100741978	CACAATTTTCAGAAC[-/CTACT]CTTGTCATTAAGCAA	10342
rs777544718	snp	A/C			downstream-variant-500B	TFG, ABI3BP	GRCh38.p7	3:100748992	AAATTTTAATTTAGT[A/C]ACTAACATTATGTGA	10342
rs777546498	snp	A/C	1.74811e-05	0.00295639	intron-variant	TFG	GRCh38.p7	3:100713885	GTAAGAGTGTTTTTA[A/C]AGCTATTTTTTAAAG	10342
rs777562750	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100711892	AGTAGTTCCTGAATA[C/T]CGAAAGCATTGCAGA	10342
rs777606172	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100716525	GATTTCTCTTCAATA[C/T]ACTGGTTTCCTTTCC	10342
rs777654574	snp	A/G	1.65696e-05	0.00287828	missense	TFG	GRCh38.p7	3:100732642	AAAAATGTTATGTCA[A/G]CGTTTGGCTTAACAG	10342
rs777663613	in-del	-/T	4.307e-05	0.00464038	intron-variant	TFG	GRCh38.p7	3:100719931	ATACAAATCTGAAAA[-/T]TTTAAAAAATTAAAA	10342
rs777664032	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100735707	CTTTTTTGACTGTCA[C/T]AGCATTGGAACTGTA	10342
rs777688107	snp	A/G	1.651e-05	0.0028731	missense	TFG	GRCh38.p7	3:100713726	GGAAGCTAATCATCA[A/G]AGCTCAACTTGGGGA	10342
rs777712960	snp	G/T			intron-variant	TFG	GRCh38.p7	3:100734884	TATGTTGAATTATAG[G/T]AGGAAAAACTGTATG	10342
rs777782723	snp	C/G			intron-variant	TFG	GRCh38.p7	3:100732243	TTGTATTTTTTTCAT[C/G]TAATGTTTCTTACAA	10342
rs777843693	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100724885	ATCATGTTGAAAAGT[C/T]GTAGCAAACTATGAA	10342
rs777898865	in-del	-/AT	1.65272e-05	0.0028746	intron-variant	TFG	GRCh38.p7	3:100736738	TAGAGTTTAGAACAC[-/AT]GTTTGGGAAAGTACA	10342
rs777959308	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100721469	TTTAGAAAAGTCTAC[C/T]TTGATACAGGGAAAG	10342
rs777971787	in-del	-/AT			intron-variant	TFG	GRCh38.p7	3:100747266	TTCATGGACTATGTC[-/AT]AAAGGTTTCTTTCAT	10342
rs778011783	snp	C/G			intron-variant	TFG	GRCh38.p7	3:100712183	AGATATTAATTTAAG[C/G]ACTAGTTAGATGGAA	10342
rs778013117	snp	G/T			intron-variant	TFG	GRCh38.p7	3:100733656	GTCACATTTTTCTGT[G/T]TCTTTGCCTGTCTGA	10342
rs778046364	snp	A/G			upstream-variant-2KB	TFG	GRCh38.p7	3:100708546	TGACAAACATTCTCC[A/G]TTTGGCCAAACTTCG	10342
rs778101625	snp	G/T			intron-variant	TFG	GRCh38.p7	3:100719794	ATAAGCAAAATTGAT[G/T]TAGTATATTTTTGAA	10342
rs778132572	snp	A/G	4.95987e-05	0.00497965	missense	TFG	GRCh38.p7	3:100748296	AGTACCAGGCGAGCA[A/G]TTATCCTGCACAAAC	10342
rs778367465	snp	G/T			intron-variant, upstream-variant-2KB, utr-variant-5-prime	TFG	GRCh38.p7	3:100710036	AGTGCGCCAGCTAAT[G/T]CCTTGGTGCAGCCTG	10342
rs778390629	snp	C/G	1.74885e-05	0.00295701	intron-variant	TFG	GRCh38.p7	3:100728679	CTTATTCATGAACTT[C/G]TAATTTTAAGCAAAT	10342
rs778395973	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100740073	CTTTGCATTGTTAAT[A/G]TGTCTTGAGTCGTTT	10342
rs778430201	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100724081	ATGACTTCTATGTAA[C/T]CAAGTTTTTAGAGAA	10342
rs778438842	snp	A/T	3.36151e-05	0.00409957	intron-variant	TFG	GRCh38.p7	3:100719966	ACCTTTTTTTTTTTT[A/T]AATTCCAGATGGAGA	10342
rs778479554	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100735875	TCTTTAAGAGGGAAA[A/G]TGAGAGCTATTCAGA	10342
rs778506905	snp	A/G	1.64844e-05	0.00287087	missense	TFG	GRCh38.p7	3:100748392	CTCCAAGCCAACCTG[A/G]GGCCTATCAACCAAG	10342
rs778539872	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100724127	TAGAGTAGTACTTAC[A/G]GCCTTAAATACTTTA	10342
rs778631802	snp	A/G	1.76216e-05	0.00296825	intron-variant	TFG	GRCh38.p7	3:100728661	TTGCATATTATTAGT[A/G]TACTTATTCATGAAC	10342
rs778824685	in-del	-/T			upstream-variant-2KB	TFG	GRCh38.p7	3:100708459	TAAGTTTTTCTTTTA[-/T]AACTGGTAAACAACT	10342
rs778916909	snp	C/G	3.37929e-05	0.00411039	intron-variant	TFG	GRCh38.p7	3:100732494	AGTTTTTGTTTATTC[C/G]TCTATTTTTACAGAT	10342
rs778999225	snp	C/G			intron-variant	TFG	GRCh38.p7	3:100734646	TTGTTACCTGGGAGA[C/G]AGTTTATCTGATGGA	10342
rs779026404	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100713233	GAGTTATTTTAAAGG[C/T]AGTGGCAACCATATT	10342
rs779042645	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100728177	TAAGATCAGCTATTT[C/T]AGTTAGCTGTTTTTT	10342
rs779137562	snp	C/T			upstream-variant-2KB	TFG	GRCh38.p7	3:100709236	AACAGCGCACTACGC[C/T]CCGCCCATTGGCGAG	10342
rs779143904	snp	G/T			intron-variant	TFG	GRCh38.p7	3:100722810	AAGTAAAAATACTTT[G/T]AAAGACTGAGAATTT	10342
rs779373748	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100741363	GGCCTAGGCTAATGT[A/G]TATGTTTGTGTCATA	10342
rs779397822	snp	C/G			missense	TFG	GRCh38.p7	3:100744844	TCAGGTCAGATGTAC[C/G]AACAGTACCAGCAAC	10342
rs779462910	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100717111	ATGAAATCTTTTCCC[A/G]ACCTATTAAAGAGGT	10342
rs779496708	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100737815	GCACTTTGGGAGGCC[A/G]AGCCAGGAGGATCAC	10342
rs779498234	snp	A/G	1.66643e-05	0.0028865	synonymous-codon	TFG	GRCh38.p7	3:100748270	ACAACTGCCTGCTCA[A/G]CCGCCACAGCAGTAC	10342
rs779532304	snp	A/C	1.66059e-05	0.00288144	synonymous-codon	TFG	GRCh38.p7	3:100748276	GCCTGCTCAGCCGCC[A/C]CAGCAGTACCAGGCG	10342
rs779553427	snp	C/T	0.000366502	0.0135321	intron-variant	TFG	GRCh38.p7	3:100719954	AATTAAAAAACAACC[C/T]TTTTTTTTTTTAAAT	10342
rs779563177	snp	C/G/T	3.38302e-05	0.00411269	missense, synonymous-codon	TFG	GRCh38.p7	3:100748153	TGCCTTTTCAGCAAG[C/G/T]TATAGTCAGCAGACT	10342
rs779567860	snp	C/G			intron-variant	TFG	GRCh38.p7	3:100713338	AAGATAAAGAAGCCT[C/G]TAGGAGAGGCAGGTT	10342
rs779603038	in-del	-/T			intron-variant	TFG	GRCh38.p7	3:100737015	AGTTCAGACTGGTGA[-/T]TTTCACACTTTATTT	10342
rs779605524	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100729501	GGACTGACCTTTAAG[C/T]ATGTGTTAATGACTT	10342
rs779618813	in-del	-/A			intron-variant	TFG	GRCh38.p7	3:100713907	TTTTAAAGTCTTTTT[-/A]AAAAAAAAAAAAAAA	10342
rs779684384	snp	A/C/G	7.50259e-05	0.0061244	intron-variant	TFG	GRCh38.p7	3:100713898	TAAAGCTATTTTTTA[A/C/G]AGTCTTTTTAAAAAA	10342
rs779839508	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100714425	GAATTACTTGAACCC[A/G]GGAGGTGGAGCTTAC	10342
rs779907886	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100746231	TTAATCTCGGGATTT[C/T]GGTCCTCACTATGCT	10342
rs779913597	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100721939	GCGGATTGCCTGAGT[A/G]CAGGAGTTCGCGACC	10342
rs779938080	snp	A/G			intron-variant, upstream-variant-2KB	TFG	GRCh38.p7	3:100710554	CCTCAGGAGGTGCTT[A/G]AGCCACAGCCTCTGA	10342
rs780113476	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100736557	TGGATACTAAACTGA[C/T]TTTTTTTTGACTATC	10342
rs780169436	snp	A/C	0.000227896	0.0106722	utr-variant-3-prime	TFG	GRCh38.p7	3:100748549	AGGCTCCTCTACACC[A/C]ATTAATGTAGCTGCT	10342
rs780219953	snp	A/C	3.30797e-05	0.00406679	missense	TFG	GRCh38.p7	3:100728838	GAGAACCAGGACCTT[A/C]CACCAATATTCCTGA	10342
rs780283780	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100742976	CAGGAGTTCCTTACT[C/T]ATTGATGACCACAGT	10342
rs780350066	snp	A/G	1.7288e-05	0.00294002	intron-variant	TFG	GRCh38.p7	3:100732471	TGAATATAGATAAAA[A/G]GGAAACAAGTTTTTG	10342
rs780378420	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100741781	CATATTTTCACTGTA[C/T]CTTTTTTATGTTTTG	10342
rs780425792	snp	G/T			intron-variant	TFG	GRCh38.p7	3:100729393	ATTTTTTCCCCATTG[G/T]ATAATGACATGTACT	10342
rs780483601	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100713384	GGAATTTATTTTTAG[A/G]TATATTAAGAAAAAT	10342
rs780514051	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100730655	AGAACCTGTGGCTTA[C/T]CCTCACCAAGAAATG	10342
rs780516926	snp	G/T			intron-variant	TFG	GRCh38.p7	3:100740008	CTAATTGTTTCAAGA[G/T]TCGTTTGTTAAATTG	10342
rs780630673	in-del	-/AC			upstream-variant-2KB	TFG	GRCh38.p7	3:100708964	CAGCTTTTGTCCTTT[-/AC]ACAGTTACAGATTTT	10342
rs780736379	snp	C/T	1.64792e-05	0.00287042	missense	TFG	GRCh38.p7	3:100744883	TATGGTGCACAGCAG[C/T]CGCAGGCTCCACCTC	10342
rs780745398	snp	G/T			intron-variant	TFG	GRCh38.p7	3:100718338	CAGCAAACATTTTCT[G/T]TAATAGATCAGAGAG	10342
rs780756667	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100739163	GTCAGTTATTTAGAT[C/T]AACTACTGGTTATAA	10342
rs780787806	snp	A/G	1.64947e-05	0.00287177	synonymous-codon	TFG	GRCh38.p7	3:100713733	AATCATCAAAGCTCA[A/G]CTTGGGGAGGATATT	10342
rs780789453	snp	C/T	5.25666e-05	0.00512645	intron-variant	TFG	GRCh38.p7	3:100748135	GATACATGTTATTTA[C/T]TTTGCCTTTTCAGCA	10342
rs780805856	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100715489	ACTTAGCACAACTTA[C/T]ACTGTGGAGGAGAAG	10342
rs780860951	snp	A/T			intron-variant	TFG	GRCh38.p7	3:100727843	TTATATTTATTTTTT[A/T]AAATTTTTTGAGACA	10342
rs780861077	snp	C/G/T			intron-variant	TFG	GRCh38.p7	3:100714592	CAAGCATTATTTTCT[C/G/T]CTTTTGTCCATATAA	10342
rs780912232	snp	C/T	3.73769e-05	0.00432285	intron-variant	TFG	GRCh38.p7	3:100713891	GTGTTTTTAAAGCTA[C/T]TTTTTAAAGTCTTTT	10342
rs780983041	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100723039	AAACCTTGGGCTGTC[A/G]GGGGATTGGGAAGCA	10342
rs781206996	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100743276	TTTTTTTATTGTGGA[A/G]TTAAGCCTTCTAATT	10342
rs781260646	in-del	-/AAAAAAA	0.000608129	0.0174268	intron-variant	TFG	GRCh38.p7	3:100713908	TTTTAAAGTCTTTTT[-/AAAAAAA]AAAAAAAAAAGACAG	10342
rs781269738	snp	A/T			intron-variant	TFG	GRCh38.p7	3:100713044	GTTTTGAACAGAATG[A/T]TACTAGGTTTTACTT	10342
rs781323715	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100734798	ATTTTGATTTAAATG[C/T]AGTATATTCCAGACT	10342
rs781349955	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100719140	TTGTCATCTTTGCCC[A/G]AAATAAATCCAACTA	10342
rs781388759	snp	C/G			intron-variant	TFG	GRCh38.p7	3:100726996	GGTAAAGTAGTAGCA[C/G]TTACTCATATTAGCC	10342
rs781399393	snp	G/T			intron-variant	TFG	GRCh38.p7	3:100712851	TTAACACTTGATAAG[G/T]AATCTGAATCATATG	10342
rs781469450	snp	C/G			intron-variant	TFG	GRCh38.p7	3:100718421	TTACAATGTAAAAAC[C/G]ATTTTTCATTCACAG	10342
rs781480581	snp	C/T	3.29837e-05	0.00406088	synonymous-codon	TFG	GRCh38.p7	3:100728810	CGTTTATTGGATAGC[C/T]TGGAACCACCTGGAG	10342
rs781504257	snp	A/C	1.64925e-05	0.00287158	missense	TFG	GRCh38.p7	3:100748448	AGTACCATGACCCCT[A/C]CTCCAAGTGGGCCTA	10342
rs781524559	snp	C/T			intron-variant	TFG	GRCh38.p7	3:100730779	AAGATTGACCTGTTG[C/T]AGTATCTCCAGCAGC	10342
rs781669290	in-del	-/AG			intron-variant	TFG	GRCh38.p7	3:100724768	CACCCAAGGAGTCTA[-/AG]AGATTGCTTTAAATT	10342
rs781710527	snp	A/G	1.70589e-05	0.00292047	intron-variant	TFG	GRCh38.p7	3:100728908	TTCTTACGTCTTTTT[A/G]GAGGTTTTAAAAAAC	10342
rs781759972	snp	C/T			upstream-variant-2KB	TFG	GRCh38.p7	3:100709173	TAACGACAAAAACCA[C/T]TTAAAGTTGGACAGA	10342
rs796111738	in-del	-/A			intron-variant	TFG	GRCh38.p7	3:100738086	AAAACAAACAAAGCC[-/A]AAAAAAAAAAAATCC	10342
rs796348999	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100732869	TAGATGATTTCCAGC[A/G]CTTCAGAAAGCTTTC	10342
rs796588365	in-del	-/A			intron-variant	TFG	GRCh38.p7	3:100742891	TTTATGAAAACATGC[-/A]AAAAAAAAAAGCTTT	10342
rs796729574	snp	A/G			intron-variant	TFG	GRCh38.p7	3:100715958	TTTAATTGACAAATA[A/G]TAATTGTACATATTT	10342
rs796825838	in-del	-/T			intron-variant	TFG	GRCh38.p7	3:100714575	CACATACATTTTTTT[-/T]ACAAGCATTATTTTC	10342
rs796880682	snp	C/G			intron-variant	TFG	GRCh38.p7	3:100721877	TAAAAGCAGCCGGCC[C/G]TGGTGGCTCACGCCT	10342
rs796898302	multinucleotide-polymorphism	CG/GA			intron-variant	TFG	GRCh38.p7	3:100736985	AGTGGTGACCCTTGG[CG/GA]GGGAGGATAGTGAAG	10342
rs796926741	in-del	-/TT			intron-variant	TFG	GRCh38.p7	3:100744807	ACATGCCTTTTTTCC[-/TT]GTGTGTGTGTGTGTG	10342
rs796934283	in-del	-/TG			intron-variant	TFG	GRCh38.p7	3:100720280	ACAGAGTGTTAAGTA[-/TG]TTTTTTTTGAAATCA	10342
rs797002439	in-del	-/AA			intron-variant	TFG	GRCh38.p7	3:100738097	AGCCAAAAAAAAAAA[-/AA]TCCACAGAGTTGTCT	10342

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