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

FANCD2

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs3826	snp	A/C	0.366885	0.220993	intron-variant, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10099381	cctaccttggcctca[A/C]aaagtgctaggatta	2177
rs166485	snp	A/G/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10083849	ccaggctggagtgca[A/G/T]tggcgcgatctcggt	2177
rs174728	snp	G/T	0	0	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092935	ggaggctgaggctgg[G/T]ggatcactagagccc	2177
rs200167	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10050554	ctcactgcaagctcc[A/G]cctcctgggttcacg	2177
rs200168	snp	A/G	0.100944	0.200705	intron-variant	FANCD2	GRCh38.p7	3:10050539	gcctcctgggttcac[A/G]ccattctcctgcctc	2177
rs200169	snp	C/G	0	0	intron-variant	FANCD2	GRCh38.p7	3:10052628	ggttcaagcgattct[C/G]ctgcctcagcctccc	2177
rs266884	snp	G/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10083892	ttttttttttttttt[G/T]ttttgagacggagtc	2177
rs266885	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10083885	tttttttttttttga[A/G]atggagtcttgctct	2177
rs266886	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10083875	tttgagacggagtct[C/T]gctctgtcgcccagg	2177
rs271993	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10050617	ttttttttttgagac[A/G]gagtcttgctctgtc	2177
rs271994	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10050595	tgctctgtcgcccag[A/G]ctggagtgcagtggt	2177
rs271995	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10055545	gattacaggcgtgag[C/T]caccgtgcccggcca	2177
rs271996	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10055608	agccaggatggtctc[A/G]atctcctgacctcat	2177
rs365100	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10075240	caggctggagtgcag[G/T]ggcgcggatctccac	2177
rs375954	snp	A/G	0	0	intron-variant	FANCD2	GRCh38.p7	3:10072281	aaaaaaaaaaaaaaa[A/G]GGGAAAGGTAtatat	2177
rs401900	snp	C/T	0	0	intron-variant	FANCD2	GRCh38.p7	3:10076148	GCTATATTACACTGC[C/T]AGAAGCAGAATGGGT	2177
rs419999	snp	C/G	0.00597247	0.0543191	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10089116	tgtatttttagtagg[C/G]acagggtttcactat	2177
rs455913	snp	A/C/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10059731	gaatggcatgaagcc[A/C/G]ggaggtggagctagc	2177
rs460965	snp	A/G	0.0153892	0.0863585	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10081243	CTTAGCAGCTTCTAA[A/G]TCTAGGCTTCTGACC	2177
rs462262	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10091435	atccaggttggagtg[C/T]agtggtgcaaacttg	2177
rs462674	snp	C/T	0.0126979	0.078662	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10091068	agaaaaaaCATATAC[C/T]GGCTGTAGCTTCTCT	2177
rs626693	snp	A/G	0.040671	0.13668	intron-variant	FANCD2	GRCh38.p7	3:10044394	GATGATTGGCCGGGC[A/G]CGGTAGCTCACGCCT	2177
rs664233	snp	A/G	0.000733235	0.0191332	intron-variant	FANCD2	GRCh38.p7	3:10043596	GCCTGGATTAAGGTG[A/G]GATCTTTGGAACTTT	2177
rs722509	snp	A/T	0.295599	0.245806	intron-variant	FANCD2	GRCh38.p7	3:10060693	CTGATTCTTTTAGAA[A/T]GCATTTTTCTTTATC	2177
rs722510	snp	C/G	0	0	intron-variant	FANCD2	GRCh38.p7	3:10060738	GCACTAGACAATGCA[C/G]GTGTCTACATTGCTG	2177
rs780961	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10079339	ccagcctgggagaca[C/G]agcgagactccgtct	2177
rs781871	snp	A/T	0.31503	0.241394	upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10025121	ACTGCACCTGGCTAA[A/T]GTTTAAATTTTTTTG	2177
rs803334	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10030793	cctgcctcagcctcc[C/T]gagtagctgagatta	2177
rs803335	snp	A/C	0.0905309	0.192535	intron-variant	FANCD2	GRCh38.p7	3:10043351	ATAAACTTGCACTGT[A/C]GTCTGTCTGGGATTG	2177
rs803336	snp	A/G	0.332568	0.235971	intron-variant	FANCD2	GRCh38.p7	3:10054673	acacggtgaaacccc[A/G]actctactaaaaata	2177
rs803341	snp	A/G	0.0611083	0.163768	intron-variant	FANCD2	GRCh38.p7	3:10053361	caaagtccccagagt[A/G]tgatgttccccttcc	2177
rs803342	snp	A/T	0	0	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090444	aaaaaaaaaaaaaaa[A/T]TCAGCAACTTCCAAG	2177
rs812380	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10083883	tttttttttttgaga[C/T]ggagtcttgctctgt	2177
rs1008636	snp	G/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092684	aaaaaaaaaaaaaaa[G/T]ACATGAAAGAGGTGG	2177
rs1066724	snp	A/C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10069309	acccatttttcaatc[A/C/T]gaataattttttttc	2177
rs1151609	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10041049	gtaccaccacgccca[C/G]ctaatttttgtatgt	2177
rs1179924	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10089281	tttttttttttgaga[C/T]ggagtttcgctcttg	2177
rs1552244	snp	A/G	0.381308	0.21274	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093893	ATGTGGGAGATGGGC[A/G]AGTTGGAGAGAGGAG	2177
rs1642642	snp	C/G	0	0	intron-variant	FANCD2	GRCh38.p7	3:10055072	TGCTAAATGCAAAAG[C/G]TAAGATGTAGAACAA	2177
rs1703145	snp	A/G	0	0	intron-variant	FANCD2	GRCh38.p7	3:10036278	TGGCAGGCTAAAAAA[A/G]AAGACATAGGGAGTT	2177
rs1798959	snp	A/C/G	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10055236	tggttgtataacatt[A/C/G]tgaatatacttaatg	2177
rs1798960	snp	A/C			intron-variant	FANCD2	GRCh38.p7	3:10055152	tattttatcaaaatt[A/C]aaaaataaaaTAAAA	2177
rs1798966	snp	A/G	0	0	intron-variant	FANCD2	GRCh38.p7	3:10036275	CAGGCTAAAAAAAAA[A/G]ACATAGGGAGTTAGG	2177
rs1983415	snp	C/G	0.267091	0.249415	intron-variant	FANCD2	GRCh38.p7	3:10046275	AGTCAGGATGGTCTC[C/G]ATCTCCTGACCTTGT	2177
rs1983416	snp	A/G	0.0618563	0.164627	intron-variant	FANCD2	GRCh38.p7	3:10046327	CAAAGTGCTGGGATT[A/G]CAGATGTGAGCCACT	2177
rs2075310	snp	A/G	0.459801	0.135955	upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10025967	GCAGGCGTTGTGTCA[A/G]TTTGCCTAGGTTCAC	2177
rs2160869	snp	C/T	0.333952	0.235483	intron-variant	FANCD2	GRCh38.p7	3:10037571	TCCAATTTTAGTATA[C/T]GTGCTGCCAAAGCAA	2177
rs2241276	snp	A/G	0.0146672	0.084371	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088704	GTATAAAACAGAACC[A/G]GAGGATCTTAAGATC	2177
rs2272123	snp	C/T	0.310632	0.242536	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098431	TTGGTGACTCTAAGT[C/T]GATGCTGAACATGGT	2177
rs2272124	snp	A/G	0.303931	0.244114	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096505	ACAAAGAATAAGAGT[A/G]GGGGATTATCACTAG	2177
rs2272125	snp	A/C	0.30382	0.244138	synonymous-codon, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096385	GACTCTGCAAACTAA[A/C]AGTTCCAGGGTCTTT	2177
rs2276798	snp	C/G	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10060658	CCCATTTTGTGCAAA[C/G]ATTTCTAGAATTTTA	2177
rs2287435	snp	A/C	0.00398564	0.0444627	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090218	GGAAGAACCAGGAAC[A/C]AAAAGTAGCTTCCTT	2177
rs2287439	snp	A/C	0.115088	0.210473	intron-variant	FANCD2	GRCh38.p7	3:10044132	TGGCTTCTTTGACTG[A/C]ACCTTGATGTGCTTG	2177
rs2302844	snp	A/G	3.36831e-05	0.00410371	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10095190	ATCTTCCTATAACCA[A/G]TAAGTTTATAAATGC	2177
rs2347581	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10064196	AAAAGAGAGAGTGCA[C/T]AAAAAGCACTTAGCA	2177
rs2347582	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10064195	AAAGAGAGAGTGCAT[A/G]AAAAGCACTTAGCAC	2177
rs2347583	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10064183	CATAAAAAGCACTTA[G/T]CACAAGGCCCAGCAC	2177
rs2347584	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10064173	ACTTAGCACAAGGCC[C/T]AGCACAGAATAGGGC	2177
rs2347585	snp	C/T	0.0501905	0.150254	intron-variant	FANCD2	GRCh38.p7	3:10064163	AGGCCCAGCACAGAA[C/T]AGGGCTCTCAGACAG	2177
rs2347586	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10064103	TCTCTTCTTTACTAT[C/T]GTGATTGTTATTAAG	2177
rs2600013	snp	C/G	0	0			GRCh38.p7	3:10101748	CCTGAGCCAGGGACT[C/G]TGATGGTGTTAGACA	2177
rs2600014	snp	A/C/G					GRCh38.p7	3:10101700	GTTAATAAAGACCCC[A/C/G]CTTTAAGAACAAAAT	2177
rs2662144	snp	A/C	0	0	intron-variant	FANCD2	GRCh38.p7	3:10061801	AGAATTCTGACTTCC[A/C]TAGGGTAGGGTAAAG	2177
rs2662145	snp	A/C	0.00576364	0.0533723	intron-variant	FANCD2	GRCh38.p7	3:10061615	AGTGCATATTATGTA[A/C]TAAACATtgttctaa	2177
rs2687893	snp	A/G	0.114387	0.210022	intron-variant	FANCD2	GRCh38.p7	3:10047230	TAAAATAATACAACC[A/G]TTAAATCTATTCCTA	2177
rs3095773	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10041071	gagtagctagaatta[C/T]aagtgcgtaccacca	2177
rs3100098	snp	A/C	0.497907	0.0322805	intron-variant	FANCD2	GRCh38.p7	3:10031320	GAGACGGGGTTTCAC[A/C]ATGTTAGCCAAGATG	2177
rs3105784	snp	A/G	0.499382	0.017561	intron-variant	FANCD2	GRCh38.p7	3:10031319	AGACGGGGTTTCACC[A/G]TGTTAGCCAAGATGG	2177
rs3107667	snp	A/C	0.496034	0.0443518	intron-variant	FANCD2	GRCh38.p7	3:10031344	CCGTCTCTACTAAAA[A/C]TACAAAAAATTAGCC	2177
rs3172417	snp	C/T	0.44092	0.161398	utr-variant-3-prime, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101265	TGACTCTGATTAGAC[C/T]CCAGATAAATTGTTG	2177
rs3732974	snp	C/G	0.0131889	0.080128	utr-variant-5-prime	FANCD2	GRCh38.p7	3:10028652	TGGAAACCATTTTGA[C/G]CAATGTCTTGTGCAC	2177
rs3843378	snp	C/G/T	0	0	intron-variant	FANCD2	GRCh38.p7	3:10073491	AGGAGATTACTCCAA[C/G/T]GCCTAAGAGAGTTTT	2177
rs3846170	snp	A/T			intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10026746	GCTTTTCTGGAAGCC[A/T]GATGGTATCGCACGT	2177
rs3846171	snp	C/G			intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10026747	CTTTTCTGGAAGCCA[C/G]ATGGTATCGCACGTG	2177
rs3846172	snp	A/T			intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10026748	TTTTCTGGAAGCCAG[A/T]TGGTATCGCACGTGT	2177
rs3846173	snp	G/T			intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10026749	TTTCTGGAAGCCAGA[G/T]GGTATCGCACGTGTT	2177
rs3846174	snp	A/G			intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10026751	TCTGGAAGCCAGATG[A/G]TATCGCACGTGTTAA	2177
rs3846175	snp	A/T			intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10026752	CTGGAAGCCAGATGG[A/T]ATCGCACGTGTTAAA	2177
rs3846176	snp	A/G			intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10026753	TGGAAGCCAGATGGT[A/G]TCGCACGTGTTAAAG	2177
rs3846177	snp	G/T	0.329783	0.236927	intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10026888	TTTAGCACAGGGCCC[G/T]GTACCTCGTAAATGT	2177
rs3864015	snp	C/T	0.0238492	0.106564	intron-variant	FANCD2	GRCh38.p7	3:10064460	CTGCTGGCTTGGTTG[C/T]ACTGGTGAAGTTACA	2177
rs3864017	snp	A/G	0.26124	0.249747	FANCD2	3	allele_origin=G(germline)/A(germline)	3:10064848	TCCTGTGAGGTCACC[A/G]GACCCCCATCTTTTG	2177
rs3895942	snp	C/G	0.32955	0.237006	intron-variant	FANCD2	GRCh38.p7	3:10067061	CAACAACGTGGTATA[C/G]AGAAAAAAAATCTCT	2177
rs3930484	snp	C/T	0.0607341	0.163335	intron-variant	FANCD2	GRCh38.p7	3:10046157	CTCCCGGGTTCACGC[C/T]ATTCTCCTGCCTCAG	2177
rs3936531	snp	C/T	0.0418186	0.138422	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085398	CTTTTTTCTTTCTTT[C/T]TTTTTTTTTTTTGAG	2177
rs4019705	snp	A/G	0.00279162	0.0372561	intron-variant	FANCD2	GRCh38.p7	3:10071102	caaatccccctctgc[A/G]agaaacacccaagaa	2177
rs4019706	snp	A/G	0.342358	0.232314	intron-variant	FANCD2	GRCh38.p7	3:10071178	tggcttttatccaaa[A/G]gacaggcaataacag	2177
rs4019707	snp	A/G	0.295343	0.245854	intron-variant	FANCD2	GRCh38.p7	3:10071366	aaagaaaggaaatca[A/G]tataccaaggagata	2177
rs4019708	snp	A/C	0.295343	0.245854	intron-variant	FANCD2	GRCh38.p7	3:10071387	caaggagatatctgc[A/C]ctcccatgtttattg	2177
rs4019772	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10064977	AAAAAGTTTCTCTCG[A/G]GACAAATGGTATTTG	2177
rs4019779	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10064079	GGCTCTTCTCTGAGG[C/G]CTCCTTCACTTAATA	2177
rs4019780	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10064102	ACTTAATAACAATCA[C/T]GATAGTAAAGAAGAG	2177
rs4019781	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10064120	TAGTAAAGAAGAGAT[G/T]GACTTTGTTAATGAT	2177
rs4019782	snp	C/T	1.64803e-05	0.00287052	intron-variant	FANCD2	GRCh38.p7	3:10064682	GTTTTCCCTGTAGCC[C/T]TGCGTATTCCTGAGC	2177
rs4019783	snp	A/G	0.000428491	0.0146309	intron-variant	FANCD2	GRCh38.p7	3:10064702	TATTCCTGAGCTGCA[A/G]CATCAGATTCTGGTT	2177
rs4019784	snp	A/C/T	0.00478114	0.0486627	intron-variant	FANCD2	GRCh38.p7	3:10064724	ATTCTGGTTTTTCTC[A/C/T]GCAGTGACTTTCCAT	2177
rs4019785	snp	C/T	0.169463	0.236672	intron-variant	FANCD2	GRCh38.p7	3:10064924	TGTTTTGAATGTTCA[C/T]GGGGAATTCCACAGC	2177
rs4019786	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10064939	TGGGGAATTCCACAG[C/T]TCTTGGTGGGGAAGT	2177
rs4019792	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10064058	TTCTGCCCTACCCTG[C/T]CTCACGGCTCTTCTC	2177
rs4019853	snp	C/T	0	0	intron-variant	FANCD2	GRCh38.p7	3:10028587	TTCTCAGAATTTATC[C/T]TCTAGAGGGTAACTT	2177
rs4260416	snp	C/T	0.333491	0.235646	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10083599	ggaaatgaaagcata[C/T]gtccacCgaccaggc	2177
rs4269070	snp	C/G	0.333722	0.235565	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10084399	CAGGCTATAAATCCT[C/G]CCACCTCAGCCTCCC	2177
rs4299466	snp	C/G	0	0	intron-variant	FANCD2	GRCh38.p7	3:10070904	gcggtgcaagatgtg[C/G]tttgttaaacagatg	2177
rs4441636	snp	A/G	0.29789	0.24537	intron-variant	FANCD2	GRCh38.p7	3:10042192	TGAGCCACCGTGCCT[A/G]GCCCACAGGTCTGTT	2177
rs4501095	snp	C/G	0.295343	0.245854	intron-variant	FANCD2	GRCh38.p7	3:10053306	CACCGCATATTCTCA[C/G]TCATAGGTGGGAATT	2177
rs4622888	snp	C/T	0.333722	0.235565	intron-variant	FANCD2	GRCh38.p7	3:10042191	TTGAGCCACCGTGCC[C/T]GGCCCACAGGTCTGT	2177
rs5009357	snp	A/G	0.327741	0.237605	intron-variant	FANCD2	GRCh38.p7	3:10049249	AAAACTAGATAATAG[A/G]TGATGGGTTTGGGTT	2177
rs5009358	snp	C/T	0.0618563	0.164627	intron-variant	FANCD2	GRCh38.p7	3:10049178	GGAAATAGGTCAAGA[C/T]GGGATGGTCAAGTTA	2177
rs5029162	snp	A/T	0.0197687	0.0974348	intron-variant	FANCD2	GRCh38.p7	3:10049284	GTGATTTTAACAAAG[A/T]AGAGATTGGAGAGGC	2177
rs5029163	snp	A/T	0.296619	0.245615	intron-variant	FANCD2	GRCh38.p7	3:10049257	ATAATAGGTGATGGG[A/T]TTGGGTTGATTGTGA	2177
rs6414438	snp	C/G	0.363776	0.222609	intron-variant	FANCD2	GRCh38.p7	3:10032140	gtgagccactgtgct[C/G]ggtcggaaatatgca	2177
rs6442146	snp	C/T	0.33303	0.235809	intron-variant	FANCD2	GRCh38.p7	3:10031860	atatgcctttttttt[C/T]ctttgagacagagtg	2177
rs6442147	snp	A/G	0.364193	0.222396	intron-variant	FANCD2	GRCh38.p7	3:10036563	CTATTGGCCTGGTGC[A/G]GTGGCTCACACCTGT	2177
rs6442148	snp	C/G	0.333952	0.235483	intron-variant	FANCD2	GRCh38.p7	3:10036605	TTTGGGAAGCTGAGG[C/G]AGGAGGATTGCTTGA	2177
rs6442150	snp	C/T	0.295854	0.245759	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10080891	CTCAATCAAACACTG[C/T]TCCTACTCTACAAAA	2177
rs6764168	snp	A/G	0.29432	0.24604	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10082121	CACATCCAAAATGGA[A/G]TATGTCATCCCTAGC	2177
rs6769888	snp	C/T	0.0607341	0.163335	intron-variant	FANCD2	GRCh38.p7	3:10066087	CCAAGCACTAACCCC[C/T]GTGTGCTTCTCTAGC	2177
rs6770502	snp	A/T			intron-variant	FANCD2	GRCh38.p7	3:10053536	gtataataataataa[A/T]aataaaataaaatag	2177
rs6771931	snp	C/G	0.342358	0.232314	intron-variant	FANCD2	GRCh38.p7	3:10071724	gagggtggttaatag[C/G]ttcaaaaatataatt	2177
rs6772289	snp	C/G	0.293807	0.246132	intron-variant	FANCD2	GRCh38.p7	3:10071885	ctgcctcagcctcct[C/G]agtagccgggactag	2177
rs6772315	snp	A/G	0.29432	0.24604	intron-variant	FANCD2	GRCh38.p7	3:10071960	agatggggtttcacc[A/G]tgttggccgggcttg	2177
rs6780327	snp	A/G	0.0614824	0.164198	intron-variant	FANCD2	GRCh38.p7	3:10062014	taggagatatactta[A/G]tgctaaatgacgagt	2177
rs6781811	snp	C/T	0.342806	0.232136	intron-variant	FANCD2	GRCh38.p7	3:10080238	CTTTGTATTCACTAT[C/T]GGGTCTACtttttga	2177
rs6782602	snp	G/T	0.333952	0.235483	intron-variant	FANCD2	GRCh38.p7	3:10074857	TAAGTCATAAGGTTT[G/T]TAATAATGTGTCAGA	2177
rs6785127	snp	C/T	0.36606	0.221428	intron-variant	FANCD2	GRCh38.p7	3:10071884	cctgcctcagcctcc[C/T]gagtagccgggacta	2177
rs6785756	snp	C/T	0.0149522	0.0851617	synonymous-codon	FANCD2	GRCh38.p7	3:10049469	GTTGGTAGTGTTAAA[C/T]CCATCTGCTATGATG	2177
rs6786638	snp	C/G	0.295599	0.245806	intron-variant	FANCD2	GRCh38.p7	3:10076391	GAAAGGTATACAGAG[C/G]AATTTATAGAGAAAA	2177
rs6788609	snp	G/T	0.0108105	0.0727212	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10081881	AGATAACGGAAGGAA[G/T]TGGAAGGTACAACAT	2177
rs6789156	snp	A/G	0.365646	0.221644	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10082436	CCTAACATAAACCCA[A/G]TTTGATCCTATCCCA	2177
rs6791810	snp	C/T	0.333491	0.235646	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10082760	ACTCTGGTATCCGTT[C/T]GTGATAAAACTTAAT	2177
rs6792811	snp	A/G	0.488424	0.0751925	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10100768	GGAGGACCATAGCTT[A/G]TTTAAAATTATGCAA	2177
rs6792951	snp	A/C	0.342806	0.232136	intron-variant	FANCD2	GRCh38.p7	3:10077919	tgtgcctatagtccc[A/C]gctactcgggaggct	2177
rs6793396	snp	C/T	0.294576	0.245994	intron-variant	FANCD2	GRCh38.p7	3:10069243	atgcgagaaaatatt[C/T]gcaaactatgtatct	2177
rs6802260	snp	C/G	0.332337	0.236052	intron-variant	FANCD2	GRCh38.p7	3:10055913	agatggagtctcact[C/G]tgtcgcccaggcttg	2177
rs6802535	snp	A/G	0.29432	0.24604	intron-variant	FANCD2	GRCh38.p7	3:10056068	atttttagtagagat[A/G]ggattttgccatgtt	2177
rs6804649	snp	A/G	0.295599	0.245806	intron-variant	FANCD2	GRCh38.p7	3:10069325	gattgaaaaatgggt[A/G]aaaggtctgaataga	2177
rs6804967	snp	C/T	0.330016	0.236849	intron-variant	FANCD2	GRCh38.p7	3:10062350	ggttcaagtgattct[C/T]ctgcctcagcctcca	2177
rs6805869	snp	C/T	0.288797	0.246971	intron-variant	FANCD2	GRCh38.p7	3:10078233	AGGACTTGGGCATAG[C/T]GGATTTGGGAACAAA	2177
rs6807485	snp	C/G	0.193028	0.243422	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092636	CGTGGTTTTGCTCAG[C/G]TTGTTCCCCCAGCCT	2177
rs6807630	snp	A/T	0.295343	0.245854	intron-variant	FANCD2	GRCh38.p7	3:10053494	taactaacctgcaca[A/T]tgtgcacatgtaccc	2177
rs6807641	snp	A/T			intron-variant	FANCD2	GRCh38.p7	3:10053539	taataataataaaaa[A/T]aaaataaaatagaat	2177
rs6807846	snp	G/T	0.34989	0.229177	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092807	AAGAATCTTCCCACT[G/T]AAGCCTCTGGAGTAG	2177
rs6808853	snp	A/C/G	0.0566069	0.158427	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087869	ggtcaggctggtctc[A/C/G]aactcctgacctcgt	2177
rs6809572	snp	A/G	0.295088	0.245901	intron-variant	FANCD2	GRCh38.p7	3:10058461	tttcttctaagagaa[A/G]gttttagctcttaaa	2177
rs7426517	snp	A/G	0.0524604	0.153226	intron-variant	FANCD2	GRCh38.p7	3:10033528	tttgtgttttcttat[A/G]aaaaaataaatatCC	2177
rs7432976	snp	C/T	0	0	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10086316	GAAGACCTTATGTGG[C/T]TGAGGGGTAGGCAGT	2177
rs7610821	snp	C/T	0.36606	0.221428	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094466	TGTTCTACCTGGGCT[C/T]CTCTGGTCCACTTCA	2177
rs7612908	snp	A/G	0.295343	0.245854	intron-variant	FANCD2	GRCh38.p7	3:10047464	CATTAATGTCTATGT[A/G]CATTGAATTATTGGT	2177
rs7613239	snp	A/G	0.0663309	0.169604	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094472	ACCTGGGCTCCTCTG[A/G]TCCACTTCAGCTGTA	2177
rs7613823	snp	A/G	0.0644693	0.167566	intron-variant	FANCD2	GRCh38.p7	3:10034962	AGCTTGTGGTTATGA[A/G]CCTAACAATCAGTGT	2177
rs7615062	snp	A/T	0.0749854	0.178521	intron-variant	FANCD2	GRCh38.p7	3:10077564	tgtctcaaaaaaaaa[A/T]TTTTTTTTTCACCCA	2177
rs7615646	snp	A/C/G	0.584586	0.151126	intron-variant	FANCD2	GRCh38.p7	3:10048089	GCAAGGAGGGAACAC[A/C/G]GAAAGGGAAAATAAT	2177
rs7615764	snp	C/T	0.296873	0.245566	intron-variant	FANCD2	GRCh38.p7	3:10040908	TTTAGCATCTGTCAC[C/T]GTCTGTTGGGCGCAG	2177
rs7616334	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10056501	ttcctttcttaaaaa[C/T]ttcttttgattttta	2177
rs7619340	snp	C/T	0.289424	0.246872	intron-variant	FANCD2	GRCh38.p7	3:10066494	CTCATTTTACACATA[C/T]GAATTTCAATAGGGA	2177
rs7621551	snp	C/T	0.294576	0.245994	intron-variant	FANCD2	GRCh38.p7	3:10072521	tgacctcaggtgatc[C/T]gcgcgccttgacctc	2177
rs7622679	snp	C/T	0.0558544	0.157504	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10097818	tatgtttagagatta[C/T]agtaaagacaggcat	2177
rs7622963	snp	C/T	0.365853	0.221536	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098141	ATGAAATATATAAAA[C/T]AGCACCACAGAGAAT	2177
rs7622966	snp	C/T	0.364817	0.222075	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098149	TATAAAACAGCACCA[C/T]AGAGAATTAGCTTCC	2177
rs7625049	snp	C/T	0.334642	0.235236	intron-variant	FANCD2	GRCh38.p7	3:10073935	TGGCCCCTAAGCTCA[C/T]AGTTTTTTGTTTTTT	2177
rs7625685	snp	A/G	0.0611083	0.163768	intron-variant	FANCD2	GRCh38.p7	3:10074462	TATTTGTACTTTGAA[A/G]TTTTTATTAAAATTC	2177
rs7626117	snp	A/G	0.352622	0.227966	intron-variant, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10098987	TTTTGGGACCCAGAA[A/G]AAACAACGACACAAT	2177
rs7631678	snp	G/T	0.29789	0.24537	intron-variant	FANCD2	GRCh38.p7	3:10037132	atGTGGCCCTACCTG[G/T]TTTTTTTTAATTACT	2177
rs7633842	snp	C/T	0	0	intron-variant	FANCD2	GRCh38.p7	3:10052188	GTTGTAAGAATTTTC[C/T]CAGTTTATATCCAGT	2177
rs7633855	snp	A/C			intron-variant	FANCD2	GRCh38.p7	3:10052220	TATCAAACCTTTGGG[A/C]TCTGAGCATAGCTTT	2177
rs7637888	snp	C/T	0.298144	0.245321	intron-variant	FANCD2	GRCh38.p7	3:10039038	TCCCTTCTCTCTAAA[C/T]CCTCCCTGGATGTAG	2177
rs7639624	snp	A/G	0.333491	0.235646	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10083658	ctttgggaggccgag[A/G]cgggcagatcatgag	2177
rs7639696	snp	C/G	0.342806	0.232136	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10083720	ggtgaaactccgtct[C/G]tactaaaaatacaaa	2177
rs7640863	snp	C/G/T	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10079179	aacccaggaggcaga[C/G/T]gctgcagtgaaccaa	2177
rs7641192	snp	G/T	0.461703	0.132974	intron-variant	FANCD2	GRCh38.p7	3:10079420	agcgattctcctgct[G/T]cagcctcctgagtag	2177
rs7646073	snp	A/G	0.333491	0.235646	intron-variant	FANCD2	GRCh38.p7	3:10055721	ggaagctgaagcagg[A/G]gaatggcgtgaaccc	2177
rs7647987	snp	A/G	0.36606	0.221428	intron-variant, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10099012	CACAATCTTAGAATC[A/G]CTCCTGAGTATCTCG	2177
rs7648057	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10052525	ATGTTGGGAAAGAtt[C/T]ttttttttttgagac	2177
rs7648104	snp	A/C	0.29789	0.24537	intron-variant	FANCD2	GRCh38.p7	3:10031627	TCTTGTTTCTTATTT[A/C]TTTTTATGGGTTGAA	2177
rs7649243	snp	A/T	0.294064	0.246086	intron-variant	FANCD2	GRCh38.p7	3:10047786	TGTGTAAAACAAAGA[A/T]TAAGATTTCCTAAGT	2177
rs7649415	snp	G/T	0.0115603	0.0751433	intron-variant	FANCD2	GRCh38.p7	3:10056925	agtggtgttatcttg[G/T]cttactgcaacctcc	2177
rs7651058	snp	C/T	0.326976	0.237854	upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10025280	TTTTTTGATGGCCTA[C/T]CATGTGCCTTGCACT	2177
rs7652190	snp	A/G	0.288127	0.247076	intron-variant	FANCD2	GRCh38.p7	3:10063466	aaaaGCTATTTGAGA[A/G]AGAAAACAGAGAGCC	2177
rs7653132	snp	A/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10051449	CAGTGTTGGACACTG[A/T]AAAAGTTGAAGATGG	2177
rs7653136	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10051451	GTGTTGGACACTGAA[A/G]AAGTTGAAGATGGAG	2177
rs9681560	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10052659	aagtggctgggacta[C/T]aggcacgtgccacca	2177
rs9681567	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10052648	ctcagcctcccaagt[A/G]gctgggactacaggc	2177
rs9681570	snp	A/G/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10052714	catcaaaaagtgggc[A/G/T]aaggacatgaacaga	2177
rs9682264	snp	C/G/T			intron-variant	FANCD2	GRCh38.p7	3:10052534	AAGAttttttttttt[C/G/T]tgagacagagtctag	2177
rs9809061	snp	C/G	0.289901	0.246826	intron-variant	FANCD2	GRCh38.p7	3:10043446	AGTTCTTTTCTGGTA[C/G]GTAGAAGAGTAATTT	2177
rs9809716	snp	C/T	0.015601	0.0869317	synonymous-codon	FANCD2	GRCh38.p7	3:10064831	GTTTTCTCAGGACTT[C/T]GCAAAAGATGGGGGT	2177
rs9811771	snp	A/G	0.310023	0.242687	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092265	AAGGTGAGTATGGAG[A/G]CTGCTTGACACATCT	2177
rs9813284	snp	A/T	0.0573587	0.15934	intron-variant	FANCD2	GRCh38.p7	3:10040715	TAGAAGTATTTTTTT[A/T]AAATTCAGTTTGTAA	2177
rs9813647	snp	A/T	0.0383715	0.133092	intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10027305	CAAACTCCCTTAGGG[A/T]TAGGAggaacacttt	2177
rs9815335	snp	C/T	0.21303	0.247251	intron-variant	FANCD2	GRCh38.p7	3:10045136	gttgccctgaataca[C/T]gcccaatGTTTTCTC	2177
rs9819824	snp	C/T	0.207253	0.246318	intron-variant	FANCD2	GRCh38.p7	3:10045694	gcaacctctgtcacc[C/T]gggttcaagcgattc	2177
rs9820100	snp	A/G	0.333952	0.235483	intron-variant	FANCD2	GRCh38.p7	3:10075786	cacaggctggagtgc[A/G]gtggtgggatcttgg	2177
rs9820598	snp	C/G	0.334412	0.235318	intron-variant	FANCD2	GRCh38.p7	3:10076228	AACATTAGAGGAAAA[C/G]AAGTATGAAAGGATT	2177
rs9820818	snp	A/T	0.0569829	0.158885	intron-variant	FANCD2	GRCh38.p7	3:10037140	CTACCTGTTTTTTTT[A/T]AATTACTATGTtaag	2177
rs9824585	snp	C/T	0.34303	0.232046	intron-variant	FANCD2	GRCh38.p7	3:10073118	TTAGATTTATAAATA[C/T]ACTGTAATTTAGGGT	2177
rs9825871	snp	A/G	0.334182	0.235401	intron-variant	FANCD2	GRCh38.p7	3:10046838	AGATTTTTGAATTTT[A/G]TTTTTGCATTAATCA	2177
rs9827740	snp	C/T	0.333261	0.235728	intron-variant	FANCD2	GRCh38.p7	3:10078847	tggtgcagctatagt[C/T]ccagctacttgggag	2177
rs9832329	snp	C/T	0.0603597	0.1629	intron-variant	FANCD2	GRCh38.p7	3:10058427	tgccgaatccaaggt[C/T]atgaaagttttcttt	2177
rs9833228	snp	C/G	0.0151433	0.0856874	intron-variant	FANCD2	GRCh38.p7	3:10028733	TCCAGTAAGTATCTA[C/G]TCATTTGTTGCTTTA	2177
rs9833504	snp	C/T	0.0748431	0.178382	intron-variant	FANCD2	GRCh38.p7	3:10080131	tgttggccaggattg[C/T]cttgatctcttgacc	2177
rs9835189	snp	A/G	0.103082	0.202275	intron-variant	FANCD2	GRCh38.p7	3:10054112	agctactcaggaggc[A/G]gaggtgggaggatcc	2177
rs9835472	snp	A/G	0.0573587	0.15934	intron-variant	FANCD2	GRCh38.p7	3:10054238	ataaataaataaaAC[A/G]AAGAGATTAGATTGG	2177
rs9836605	snp	A/C	0.0752113	0.178743	intron-variant	FANCD2	GRCh38.p7	3:10072118	aataacttactgtac[A/C]tttaaaaataactaa	2177
rs9837779	snp	C/G	0.0554779	0.157039	intron-variant	FANCD2	GRCh38.p7	3:10059573	tttgggaggccaaga[C/G]aggcggatcacgagg	2177
rs9838049	snp	A/G	0.0618563	0.164627	intron-variant	FANCD2	GRCh38.p7	3:10067034	ctggctGAATCTCCT[A/G]TATTTTGGGCCAGAG	2177
rs9845756	snp	C/G	0.333261	0.235728	upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10025864	CACCTGTCTATGAGG[C/G]AGGTACTGTTATTAT	2177
rs9845773	snp	A/C	0.0603597	0.1629	intron-variant	FANCD2	GRCh38.p7	3:10079094	aaaaatacaaaaaaa[A/C]ttagccaggtatggt	2177
rs9848896	snp	C/T	0.347914	0.230028	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10091890	ATGAAGTCAGGAGTT[C/T]GAGACTAGCCTGGCC	2177
rs9849434	snp	A/G	0.36606	0.221428	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092026	CATGTGCAGGCCTCA[A/G]AACCATCTTGTGGAT	2177
rs9851222	snp	C/G	0	0	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087205	CTCTTTATCTCATCA[C/G]ACTTTTGATGGTTAT	2177
rs9855143	snp	C/T	0.0551013	0.156571	intron-variant	FANCD2	GRCh38.p7	3:10033229	ccggcctgggcaaca[C/T]gtctctactaaaata	2177
rs9856270	snp	C/G	0.0618563	0.164627	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088151	TGGCCTTCCCACTGC[C/G]CAGCAGCATTCCTTT	2177
rs9859815	snp	C/G	0.0482946	0.147699	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093886	TTGCGCAATGTGGGA[C/G]ATGGGCAAGTTGGAG	2177
rs9862958	snp	A/G	0.15698	0.23205	intron-variant, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10099488	aatAAACctgggtgc[A/G]gtggctcacacctgt	2177
rs9869743	snp	A/G	0.0577344	0.159793	intron-variant	FANCD2	GRCh38.p7	3:10041281	GCACCACCTACATGT[A/G]TCTCTCATACTTATC	2177
rs9873794	snp	G/T	0.340333	0.233109	intron-variant	FANCD2	GRCh38.p7	3:10032469	TGTGGAGGGGGGGAA[G/T]GGGGGTGAAGGGGGG	2177
rs9875081	snp	A/G	0.333261	0.235728	intron-variant	FANCD2	GRCh38.p7	3:10042251	TTCCATGTTGTCTGA[A/G]TCATACCTGCTTCCC	2177
rs9879080	snp	C/T	0.287812	0.247124	intron-variant	FANCD2	GRCh38.p7	3:10042540	AAACCTATTAAGTTT[C/T]TGTGCTTTTAATTTT	2177
rs9881859	snp	A/T	0.338069	0.233974	intron-variant	FANCD2	GRCh38.p7	3:10031130	AATGAACAAACTGAA[A/T]CTTTCATTCTGGTTG	2177
rs9882700	snp	A/C			intron-variant	FANCD2	GRCh38.p7	3:10078608	atccgcccaccttgg[A/C]ctcccaaagtgctgg	2177
rs10212432	snp	C/T	0.175254	0.238565	intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10027480	ATTCAGGCACTTCCC[C/T]CACCTCTGCTGTCTG	2177
rs10212541	snp	A/T	0.33303	0.235809	intron-variant	FANCD2	GRCh38.p7	3:10032569	GCCTTGGCCTCCTAA[A/T]TTGCTGGGATTACCA	2177
rs10212542	snp	C/T	0.0614824	0.164198	intron-variant	FANCD2	GRCh38.p7	3:10062701	TGGCTTGGGTAGCAT[C/T]TAtttttatgtttat	2177
rs10222446	snp	C/G/T	0.350502	0.228931	intron-variant	FANCD2	GRCh38.p7	3:10049351	TTTGTTTTACACTGT[C/G/T]CTGTTGACTCTCCCC	2177
rs11705998	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10065119	cgtggcgaaacactg[G/T]ctctactaaaaatac	2177
rs11710252	snp	A/G	0.00318978	0.0398085	intron-variant	FANCD2	GRCh38.p7	3:10077746	atttaaaaaTTCGCT[A/G]GGCccaggtgtggtg	2177
rs11716842	snp	C/T	0.327211	0.237778	intron-variant, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10099500	TGCGGTGGCTCACAC[C/T]TGTAATCCCAGCACT	2177
rs11720494	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10073156	TTACCTCTTCTACCT[C/T]TAGGCAGTTTCCAAC	2177
rs11921819	snp	A/G	0.0603597	0.1629	intron-variant	FANCD2	GRCh38.p7	3:10048803	ATTTAAAGTAGAGCA[A/G]TAGTTGCAGCTGACA	2177
rs11921952	snp	A/G	0.0592355	0.161582	intron-variant	FANCD2	GRCh38.p7	3:10049174	TATGGGAAATAGGTC[A/G]AGATGGGATGGTCAA	2177
rs11925559	snp	C/T	0.212122	0.247114	intron-variant	FANCD2	GRCh38.p7	3:10070033	agcgtctctgcccgg[C/T]cacccatcgtctgag	2177
rs11926481	snp	G/T	0.350982	0.228698	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10100418	tccctctgtcgccca[G/T]gctagcatgcagtgg	2177
rs12152341	snp	A/G	0.366473	0.221211	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096942	ATTTTCCTAAGTGTC[A/G]GCTGGCTTGAGAAAT	2177
rs12152512	snp	C/T	0.36606	0.221428	downstream-variant-500B, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10102086	AAGAACCAACTTCAT[C/T]TGAGATGAGATATAT	2177
rs12152515	snp	C/T	0.364193	0.222396	downstream-variant-500B, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10102292	GGGACTACAGGCACA[C/T]GCCACCATGCCTGGC	2177
rs12152520	snp	G/T	0.350982	0.228698	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10097093	TTTCAAAAGGGGAGG[G/T]AGTGTGCGAATAGGT	2177
rs12330369	snp	A/G	0.494895	0.0502635	synonymous-codon	FANCD2	GRCh38.p7	3:10048039	TAAGTTTTTTGACAC[A/G]TACTGCCAGCAGGTA	2177
rs12330599	snp	C/T	0.490396	0.0686276	intron-variant	FANCD2	GRCh38.p7	3:10048065	AGGTATGTTGAAACA[C/T]TTATTTTGGCAAGGA	2177
rs12374115	snp	C/T	0.311369	0.242351	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093082	GGAATCAGTTTATTT[C/T]TCTTTGCTCGTCTCT	2177
rs12491122	snp	A/C			intron-variant	FANCD2	GRCh38.p7	3:10067778	actccagcctgggtg[A/C]cagagcgagactccc	2177
rs12629301	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10061714	AAAATATATAGGATA[A/G]CCATCCTTTGCTCTA	2177
rs13068708	snp	C/T			utr-variant-3-prime, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101378	CCTTTTTTGTTCCTC[C/T]ttttttttttttttt	2177
rs13070248	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10051212	ggtgaaaccccgtct[C/T]tactaaaaatacaaa	2177
rs13075146	snp	A/G	0.32768	0.237625	intron-variant	FANCD2	GRCh38.p7	3:10051330	agcttgcagtgagcc[A/G]agatcccgccactgc	2177
rs13089624	snp	A/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092688	CTCTTTCATGTCttt[A/T]ttttttttttttttt	2177
rs13098680	snp	A/C			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10091143	tggagtgtagtggtg[A/C]aaacttggctcactg	2177
rs13098715	snp	A/C			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10091197	atgatcctcccacgt[A/C]agcctcccaaatagc	2177
rs13319477	snp	C/T	0.342358	0.232314	intron-variant	FANCD2	GRCh38.p7	3:10051151	tttgggaggccgagg[C/T]gggcggatcacgagg	2177
rs13319510	snp	C/T	0.363568	0.222716	intron-variant	FANCD2	GRCh38.p7	3:10051249	agccgggcgtagtgg[C/T]gggcgcctgtagtcc	2177
rs13319597	snp	G/T	0.333952	0.235483	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10084628	TTAAGTACATGAAGT[G/T]TATTGTACATCAACT	2177
rs13323438	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094252	CCTTTCAGTGAGATA[C/T]CTCAGCTAGAGGTAA	2177
rs13326410	snp	C/T	0.333722	0.235565	intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10027821	gaggcaggagaatgg[C/T]gtgaacccgggaggt	2177
rs13433680	snp	A/T	0.347253	0.230308	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094706	TCTCAGAAATGATTT[A/T]AAAAAAAAAAAAGCT	2177
rs13434077	snp	G/T	0.0479149	0.147179	intron-variant	FANCD2	GRCh38.p7	3:10053467	caccagcatggcaca[G/T]gtatacatatgtaac	2177
rs13434249	snp	A/T	0.0479149	0.147179	intron-variant	FANCD2	GRCh38.p7	3:10053568	ataaaattaaaaaaa[A/T]tTTTTTTGTATTCTC	2177
rs17032268	snp	C/T	0.328616	0.237317	upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10026288	TGGGCCTTCTCTCGC[C/T]CCTATGCCCGGCTAG	2177
rs17032276	snp	A/C	0.296619	0.245615	intron-variant	FANCD2	GRCh38.p7	3:10035291	TTGTGGTGTATGCTC[A/C]AGTCTAAATAGCGGG	2177
rs17032277	snp	C/T	0.29789	0.24537	intron-variant	FANCD2	GRCh38.p7	3:10035339	GGTTAATTGGAGAAT[C/T]TGGGTTTGTAGCAGC	2177
rs17032278	snp	A/G	0.277143	0.248522	intron-variant	FANCD2	GRCh38.p7	3:10036271	ATCTCCTAACTCCCT[A/G]TGTCTTCTTTTTTAG	2177
rs17032279	snp	A/G	0.00196575	0.0312892	intron-variant	FANCD2	GRCh38.p7	3:10036349	TGAAAAGTAAGTGGC[A/G]TTATTATGGAATGTT	2177
rs17032283	snp	C/G	0.276692	0.248571	intron-variant	FANCD2	GRCh38.p7	3:10039861	GTGGATAAACCCTCT[C/G]TCATCATCTAAGTGA	2177
rs17032289	snp	C/G/T	0.0976427	0.19821	intron-variant	FANCD2	GRCh38.p7	3:10041861	TTTTTTTTTTTTCCC[C/G/T]TCAATGAGTTTCAGA	2177
rs17032295	snp	A/G	0.298398	0.245271	intron-variant	FANCD2	GRCh38.p7	3:10044996	TGGTCTAATAACTCA[A/G]TTTTGGTGTCCTAAG	2177
rs17032299	snp	C/T	0.298398	0.245271	intron-variant	FANCD2	GRCh38.p7	3:10045954	TTGGCAACAAATACA[C/T]GCTGGAGTTGGCAAG	2177
rs17032306	snp	C/G	0.333722	0.235565	intron-variant	FANCD2	GRCh38.p7	3:10049715	TAGGCCCTTACCTTT[C/G]ATGTTAAAGACTAAG	2177
rs17032348	snp	C/T	0.0611083	0.163768	intron-variant	FANCD2	GRCh38.p7	3:10075521	TACGGCATTAATGGT[C/T]TGAACCAAGGACTAG	2177
rs17032365	snp	A/G	0.0341408	0.126114	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088294	CAGTGGATCAGGAAC[A/G]TGACAGCTTTTTGTA	2177
rs17032380	snp	C/G	0.113685	0.209567	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098573	ATCCCTCCTCTAGAT[C/G]CTGAATCACAAGTTG	2177
rs17032386	snp	A/G	0.0607341	0.163335	intron-variant, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10099085	AGCCTCTCATTTTCC[A/G]TGAATTCATATCTGA	2177
rs17536371	snp	A/G	0.0419388	0.138602	intron-variant	FANCD2	GRCh38.p7	3:10052371	AGCCTCATTGTTGGC[A/G]TCATTTTTTCCACAG	2177
rs17608820	snp	A/G	0.0138799	0.0821421	intron-variant	FANCD2	GRCh38.p7	3:10076320	CTGTGTGTGGCATTC[A/G]AAGTCATTTTTTAAA	2177
rs17609118	snp	A/G	0.031825	0.122064	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087434	CAGAACAACCTGACT[A/G]ATTTCTGCTAAAATT	2177
rs28393527	snp	A/C	0	0	intron-variant	FANCD2	GRCh38.p7	3:10051408	AAAAAAAAAAAAAAA[A/C]AAAAAGGAGTGAGGG	2177
rs28405546	snp	C/T	0.333491	0.235646	intron-variant	FANCD2	GRCh38.p7	3:10030774	GCGTGGTGTCACGTG[C/T]CTGTAATCTCAGCTA	2177
rs28428922	snp	C/T	0.387812	0.208586	intron-variant	FANCD2	GRCh38.p7	3:10049063	TTGTACAACCTCAAC[C/T]TAAAGGGTAAAATTT	2177
rs28438417	snp	A/T			intron-variant	FANCD2	GRCh38.p7	3:10064668	GGTTTGCTCTAGTGG[A/T]TTTCCCTGTAGCCTT	2177
rs28455664	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10064661	TGAAATTGGTTTGCT[C/T]TAGTGGTTTTCCCTG	2177
rs28473100	snp	A/G	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10051414	AAAAAAAAACAAAAA[A/G]GAGTGAGGGATTTAT	2177
rs28525456	snp	C/T	0.0944967	0.195752	intron-variant	FANCD2	GRCh38.p7	3:10031309	GAGATTGAGACCATC[C/T]TGGCTAACATGGTGA	2177
rs28575370	snp	A/G	0	0	intron-variant	FANCD2	GRCh38.p7	3:10049033	TGCCATCTTTTTGAG[A/G]AATTTCAACTGATCT	2177
rs28654079	snp	A/G	0.0603597	0.1629	intron-variant	FANCD2	GRCh38.p7	3:10052140	GTTTCCTGATAGTTA[A/G]TTCCTAGTCTCTGAT	2177
rs28674015	snp	C/T	0.33303	0.235809	intron-variant	FANCD2	GRCh38.p7	3:10031499	AGAGCAAGACTCCAT[C/T]TCAAAAAAAAAAAAA	2177
rs28674575	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10041875	CCTCAATGAGTTTCA[A/G]ATGCTATTCTATGGT	2177
rs28684871	snp	A/C	0.363776	0.222609	intron-variant	FANCD2	GRCh38.p7	3:10030951	ATTAGTAATGGGGTT[A/C]TAGAATTAGAATATA	2177
rs28810991	snp	C/T	0.0566069	0.158427	intron-variant	FANCD2	GRCh38.p7	3:10072084	TTTTTGATAGCACAA[C/T]AGGGTGACTACAGTC	2177
rs33917318	snp	C/T	0.333261	0.235728	upstream-variant-2KB, nc-transcript-variant	FANCD2, CIDECP	GRCh38.p7	3:10026113	TAGTGGCGGATCATG[C/T]CTACGAAGAGTGATA	2177
rs33956334	snp	A/G	0.00557542	0.0525036	intron-variant	FANCD2	GRCh38.p7	3:10031376	GGCGTGGTGGTGTGC[A/G]CCTGTAGTCCCAGCT	2177
rs33972700	snp	A/G	0.0715223	0.175059	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10086951	CCTGGCTTTTTCCAT[A/G]CAAAGGTATGGTTTT	2177
rs33983541	in-del	-/C/CTC	0.128976	0.218754	intron-variant	FANCD2	GRCh38.p7	3:10033807	CAGGTTCACACCATT[-/C/CTC]CTGCCTCAGCTTCCC	2177
rs33998487	snp	C/G	3.35239e-05	0.004094	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087273	AAAATTGGTGATGGG[C/G]CTAGATCCTTTTTTT	2177
rs34004365	snp	A/G	0.0209421	0.100162	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085083	ATTAATGTAGGAGAA[A/G]GGGTAAGTACCACTA	2177
rs34016180	in-del	-/A	0.0189856	0.0955633	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10086425	CTCACTTCCCTTGGT[-/A]ACCTAGACCATCACT	2177
rs34029039	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10029603	TTTTTATTTTACTAG[G/T]TTTTTTGGGAACAGG	2177
rs34044551	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10053720	TTTTCTTACCACAAA[C/T]ATTAAGTGCCTATTC	2177
rs34046352	snp	A/G	0.217138	0.247831	synonymous-codon	FANCD2	GRCh38.p7	3:10043852	AAACACTGCCTCAGT[A/G]TCTGAACACAAGGTA	2177
rs34053835	snp	A/G	0.000399281	0.0141238	synonymous-codon	FANCD2	GRCh38.p7	3:10065454	ACTTTGTGTGGAGAG[A/G]CAGCATAACGGAAAC	2177
rs34067296	snp	A/G	0.0543475	0.155628	intron-variant	FANCD2	GRCh38.p7	3:10031459	GTGAGCCAAGATCGC[A/G]CCACTGCACTCCAGC	2177
rs34067373	snp	A/T	0.000798403	0.0199641	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094504	CCAGAGATCCCCAAA[A/T]TGGACTGAATATTCC	2177
rs34080274	snp	A/G	0.288127	0.247076	intron-variant	FANCD2	GRCh38.p7	3:10065240	GTTGCAGTGAGCTGA[A/G]ATCGTGCCACTGCAC	2177
rs34080457	snp	C/T	0.0105817	0.0719645	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10091557	TTACTTGTCTAGCTC[C/T]GTTCTGGTTAGCAGG	2177
rs34092072	snp	C/G	0.00318978	0.0398085	intron-variant, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10099213	ATGTGAAAGCATTTG[C/G]TGAAAGCCAAAGCAC	2177
rs34112657	snp	A/C/G	0.00557925	0.0525759	intron-variant	FANCD2	GRCh38.p7	3:10061983	TGTGGGGTGGGGGAG[A/C/G]GGGGAGGGATAGCAT	2177
rs34112779	snp	C/G	0.0279526	0.114869	intron-variant	FANCD2	GRCh38.p7	3:10035920	ATTATTTTAACGTTG[C/G]CTTGATAATCATTTT	2177
rs34113138	snp	G/T	0.00725416	0.0597868	intron-variant	FANCD2	GRCh38.p7	3:10032981	CAACTAGGTAATATT[G/T]TAATCTAATTTTATT	2177
rs34115008	in-del	-/T			intron-variant	FANCD2	GRCh38.p7	3:10033698	TATCAAAGCTAAGTC[-/T]TTTTTTTTTTTTTTT	2177
rs34131370	snp	A/G	0.0325976	0.123435	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093109	CTCTTCCTTTTCTTG[A/G]ACTTCAGTTGTGATA	2177
rs34136078	in-del	-/A	0.110872	0.20771	intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10028069	AAAAAAAAAAAAAAA[-/A]TTCAAGGAGATTGTC	2177
rs34149319	snp	A/T	0.0142736	0.0832652	intron-variant	FANCD2	GRCh38.p7	3:10057791	ATTACTATTAAAATT[A/T]AAAAAAACAGCATAT	2177
rs34157687	snp	C/T	0.0614824	0.164198	intron-variant	FANCD2	GRCh38.p7	3:10063715	CAGAAAGTGAAAAAA[C/T]AGTCTTGAAAGGGGC	2177
rs34168978	in-del	-/A			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092403	TGTCCCCCTACCCAT[-/A]CCTGGATAACCCCTT	2177
rs34175149	snp	C/T	0.00755907	0.0610114	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10081635	TCATTTGATCTTGTA[C/T]CCTCTGAGTCCTTTG	2177
rs34175232	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10029618	GTTTTTTGGGAACAG[C/G]TGGTGTTCGGTTACA	2177
rs34177396	in-del	-/A	0.201664	0.245283	intron-variant	FANCD2	GRCh38.p7	3:10062128	GTATAATAATAATTT[-/A]AAAAAAAATTCTTTG	2177
rs34179822	snp	A/G	0.366266	0.221319	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098333	TGAAACCACCTCACC[A/G]TACTGTCCTTTAGCC	2177
rs34197804	snp	A/G	0.0107246	0.0724382	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087060	AAGGGACTTGGGCAC[A/G]TCATGTGGATTTAAA	2177
rs34198574	in-del	-/A			upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10024971	CACCCAGGCTGGACC[-/A]AAAAGGTCGAGGCTG	2177
rs34199062	snp	A/G	0.00953873	0.0683987	intron-variant	FANCD2	GRCh38.p7	3:10047231	AGGAATAGATTTAAC[A/G]GTTGTATTATTTTAT	2177
rs34206187	snp	A/C	0.0314385	0.121371	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10089347	CACACAACTGCCTTG[A/C]TCCTCCTCATCTAAT	2177
rs34210924	in-del	-/C			intron-variant	FANCD2	GRCh38.p7	3:10077634	ATGCCTGTCCATAAT[-/C]CCCAATACCTTGGGA	2177
rs34215311	snp	A/C	0.296109	0.245711	intron-variant	FANCD2	GRCh38.p7	3:10049115	GAGGAAAACTACGCC[A/C]AGGAGCAAAATCAGG	2177
rs34220994	snp	A/G	0.0142736	0.0832652	intron-variant	FANCD2	GRCh38.p7	3:10075566	GAGAATGATGTTTAT[A/G]TAGAAGTTGGGAGTA	2177
rs34224126	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10065296	TCTGTCTCAAAAAAA[A/G]AAGTTGTGTTCCCTA	2177
rs34242752	snp	C/G	0.00755907	0.0610114	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10082249	GTCTTTTTCCCACAT[C/G]TGATTGCCAAATCCT	2177
rs34254235	snp	C/T	0.0121208	0.0768991	intron-variant	FANCD2	GRCh38.p7	3:10040551	GGTGATTCATTCTAA[C/T]GCACAGTCCTGCATC	2177
rs34280496	snp	A/G	0.00478085	0.0486577	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093660	TTTTCTTTAAAGTCT[A/G]TGGGTGGCCTTACAA	2177
rs34288918	snp	C/T	0.0197687	0.0974348	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090147	TTACTGAGTCCTTTC[C/T]GCTCCCCCATCCTCT	2177
rs34304469	snp	C/G	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10076380	ATCCACAACTAGAAA[C/G]GTATACAGAGGAATT	2177
rs34305518	snp	A/T	0.329861	0.236901	intron-variant, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10099372	TCATGCTTGTAATCC[A/T]AGCACTTTTTGAGGC	2177
rs34309598	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098625	TGAATGGCTAAAATA[C/T]CTTCCTTTGTATTGC	2177
rs34316435	snp	G/T	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10074128	TTTTTGTATTTTTAG[G/T]AGAGACGGGGTTTCA	2177
rs34318454	snp	A/G	0.0379877	0.132479	intron-variant	FANCD2	GRCh38.p7	3:10032474	AGGGGGGGAATGGGG[A/G]TGAAGGGGGGGAGAT	2177
rs34323624	snp	A/G	0.0185644	0.0945387	intron-variant	FANCD2	GRCh38.p7	3:10065531	TCCTTTCTTCTTTAT[A/G]CTCTTCCTTTGGTAA	2177
rs34357080	snp	C/T	0.00755907	0.0610114	intron-variant	FANCD2	GRCh38.p7	3:10062329	CACTGCAACCTCCAC[C/T]TCTCAGGTTCAAGTG	2177
rs34363202	snp	A/G	0.0107246	0.0724382	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10095133	GAGCTTTTGATTGCA[A/G]GGGTATCTTGAATCT	2177
rs34366572	snp	A/G	0.0314056	0.121312	intron-variant	FANCD2	GRCh38.p7	3:10065577	AGATCAATACATGGT[A/G]TATGTGGGGAGGAAT	2177
rs34388064	snp	A/G	0.0209421	0.100162	intron-variant	FANCD2	GRCh38.p7	3:10035993	ATATTCTAAAAATGA[A/G]GACATATTCGTGTGG	2177
rs34389308	snp	A/C			intron-variant	FANCD2	GRCh38.p7	3:10054300	GTGCTACCTTATGGC[A/C]GTAATTCATACTGGA	2177
rs34398688	in-del	-/AGT	0.0341408	0.126114	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093635	AAGGGAGGAAGGAGG[-/AGT]AGATGATTTTTCTTT	2177
rs34409711	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092941	AAGTGATCCACCAGC[C/T]TCAGCCTCCCAAAAT	2177
rs34414402	in-del	-/T			frameshift-variant	FANCD2	GRCh38.p7	3:10067244	GAAACATCACCTGAG[-/T]ATGAAGGGGAAGGTG	2177
rs34417922	snp	A/C/G	0.00199529	0.0315338	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10089697	CTAGTCTTGAACCCA[A/C/G]CCTCAGGTGATCTGC	2177
rs34423558	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10072647	TATCATTATTTAAAG[G/T]GGTTTTATGATAATT	2177
rs34441486	snp	C/T	0.00676609	0.0577691	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094419	GTTGCTCAGAAGATA[C/T]GTCCTTGGTGACTCC	2177
rs34447614	snp	A/C	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10052146	TGATAGTTAGTTCCT[A/C]GTCTCTGATAATAAG	2177
rs34470023	snp	A/C	0.00119737	0.0244387	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10095737	AGCCTTCTTATAGTT[A/C]ATGAGGTATTGTCAC	2177
rs34489692	in-del	-/T	0.375	0.216506	intron-variant	FANCD2	GRCh38.p7	3:10059805	TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTCAC	2177
rs34491509	snp	C/G	0.0252325	0.109451	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10100408	AGACGGAGTCTCCCT[C/G]TGTCGCCCAGGCTAG	2177
rs34512457	snp	C/T	0.00517822	0.0506191	upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10024841	ATTCAGCAGCGTAAA[C/T]ATAGGAGAGCTAGAT	2177
rs34527587	in-del	-/GT	0.408163	0.193609	intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10026979	TGCTGAAGCCAGACT[-/GT]CCGAGTTAGAATCCC	2177
rs34545266	in-del	-/G			intron-variant	FANCD2	GRCh38.p7	3:10061930	ACAATGAGAACACAT[-/G]GGACACAGGAAAGGG	2177
rs34549096	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10062494	TGATCCACCTGCCTC[A/G]GCCTCCCAAAGTGCT	2177
rs34550475	snp	C/T	0.233235	0.249437	intron-variant	FANCD2	GRCh38.p7	3:10052734	ACATGAACAGACACT[C/T]CTCAAAAGAAGACAT	2177
rs34551164	snp	C/T	0.0134861	0.0810011	intron-variant	FANCD2	GRCh38.p7	3:10031285	AAGGCGGGCAGATCA[C/T]GAGGTCAGGAGATTG	2177
rs34557223	snp	C/G	0.00184338	0.0303033	missense	FANCD2	GRCh38.p7	3:10047974	AGTTTGCTTCACTCT[C/G]TAGACCAGAGTATAA	2177
rs34560466	in-del	-/T			intron-variant	FANCD2	GRCh38.p7	3:10047751	TGAGAGTAATCTCAG[-/T]AATGATGAAGGATTA	2177
rs34561577	in-del	-/G	0.022469	0.103584	intron-variant	FANCD2	GRCh38.p7	3:10032489	TGAAGGGGGGGAGAT[-/G]GGGGGGGTGGTCTCA	2177
rs34569725	snp	C/T	0.040671	0.13668	intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10027829	AGAATGGTGTGAACC[C/T]GGGAGGTGGAGCTTG	2177
rs34576781	in-del	-/T			intron-variant	FANCD2	GRCh38.p7	3:10061250	CTGGCTGCCCAGTGC[-/T]TTTCTTGCAACGTAC	2177
rs34599169	snp	G/T	0.00874735	0.0655527	intron-variant	FANCD2	GRCh38.p7	3:10031373	CCGGGCGTGGTGGTG[G/T]GCACCTGTAGTCCCA	2177
rs34603919	snp	G/T	0.0755793	0.179102	intron-variant	FANCD2	GRCh38.p7	3:10061709	AGAAAAAAATATATA[G/T]GATAACCATCCTTTG	2177
rs34608006	snp	G/T	0.285979	0.247398	intron-variant	FANCD2	GRCh38.p7	3:10065836	TGGCTTGCACTAAAG[G/T]TAGTTGGAAATGTTT	2177
rs34610029	snp	C/G	0.00398564	0.0444627	intron-variant	FANCD2	GRCh38.p7	3:10050244	GGAGTGAGAGTAAGG[C/G]CCAGATTTTGGTCAC	2177
rs34632086	snp	C/T	0.311614	0.242289	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10091794	CTTGGACCCAAGACA[C/T]AGAAGAATCAGCAAC	2177
rs34641718	snp	C/T	0.00953873	0.0683987	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093658	ATTTTTCTTTAAAGT[C/T]TATGGGTGGCCTTAC	2177
rs34659188	snp	A/C			intron-variant	FANCD2	GRCh38.p7	3:10054334	TGACTTTGAACAACC[A/C]GCATATATATATATA	2177
rs34672469	snp	C/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10075432	CCTCGTGATCACCCG[C/G]CTTGGCCTCCCAAAG	2177
rs34680226	snp	C/T	0.0361195	0.129442	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10091820	GCAACTACCACCGGG[C/T]GCAGTGGCGCACGTC	2177
rs34684179	snp	A/G	0.153	0.230415	intron-variant	FANCD2	GRCh38.p7	3:10031360	TACAAAAAATTAGCC[A/G]GGCGTGGTGGTGTGC	2177
rs34684855	snp	C/T	0.0952156	0.196321	intron-variant	FANCD2	GRCh38.p7	3:10043667	TATAACTGAGGTAGA[C/T]TGAAATAAAAATCTC	2177
rs34691009	snp	A/G	0.0106949	0.0723399	missense	FANCD2	GRCh38.p7	3:10032865	TTTCCAAAAAGACAA[A/G]GAAATCTCATATTGC	2177
rs34698410	snp	G/T	0.00279162	0.0372561	intron-variant	FANCD2	GRCh38.p7	3:10073953	TTTTTTGTTTTTTGT[G/T]TTTTGTTTTTGAGAT	2177
rs34742948	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10058130	ATGCCTTTGTTCTTA[C/T]TGGTGTCTGTGTAAG	2177
rs34750074	snp	A/G	0.305186	0.243833	intron-variant	FANCD2	GRCh38.p7	3:10050056	TAAGACATAGGACAG[A/G]CCCATGTTGCAAAGA	2177
rs34751191	snp	A/G	0.000345938	0.0131472	intron-variant	FANCD2	GRCh38.p7	3:10065506	CTAGGTATGGGATGA[A/G]GTCATCAGATCCTTT	2177
rs34758446	snp	A/C	0.0197687	0.0974348	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10091610	AAACAGGCTGGCTTA[A/C]CTCATGCCAGTTAGC	2177
rs34760051	snp	C/T	0.17461	0.238362	intron-variant	FANCD2	GRCh38.p7	3:10053401	GGGAGGCGGGAGGGA[C/T]AGCATTGGGAGATAC	2177
rs34765690	snp	C/T	0.332799	0.23589	intron-variant	FANCD2	GRCh38.p7	3:10033854	AGGCGCCCGCCACCA[C/T]GCCTGACTAATTTTT	2177
rs34765852	snp	C/T	0.00398564	0.0444627	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10100709	TATTTCATTCTATAT[C/T]GAATGCCCTCTTTGT	2177
rs34774358	in-del	-/GTTT	0.478674	0.101035	intron-variant	FANCD2	GRCh38.p7	3:10032668	TCTATTTGTTTGTTT[-/GTTT]TGGAAGCCACTATTG	2177
rs34777974	snp	A/G	0.00076539	0.0195476	intron-variant	FANCD2	GRCh38.p7	3:10043881	TAATGTTCATGTACT[A/G]TGCATTTTCAGTATT	2177
rs34796094	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10029646	ACATAAATAAGTTCT[C/T]TAGTGGTGATTTCTG	2177
rs34798714	snp	A/G	0.0667028	0.170006	intron-variant	FANCD2	GRCh38.p7	3:10060985	GTGGAATCCTAATTA[A/G]GGAAAAGGAGTCACA	2177
rs34810856	snp	A/G	0.0429695	0.140137	intron-variant	FANCD2	GRCh38.p7	3:10078244	ATAGTGGATTTGGGA[A/G]CAAAGGAGGTATTAT	2177
rs34824514	in-del	-/T			intron-variant	FANCD2	GRCh38.p7	3:10036616	AGGGAGGAGGATTGC[-/T]TTGAGTTCAGGAATT	2177
rs34826850	snp	A/G	0.00438332	0.0466095	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093875	TTACTCCACCCTTGC[A/G]CAATGTGGGAGATGG	2177
rs34829085	snp	A/G	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10067536	CACGAGGTGGCTCAC[A/G]CCTGTAATCCTAGCA	2177
rs34840334	snp	A/G	0.0112991	0.0743093	intron-variant	FANCD2	GRCh38.p7	3:10032471	TGGAGGGGGGGAATG[A/G]GGGTGAAGGGGGGGA	2177
rs34840725	snp	G/T	0.00795532	0.062565	intron-variant	FANCD2	GRCh38.p7	3:10052121	AGGATAAAGAAAACT[G/T]TATGTTTCCTGATAG	2177
rs34847112	snp	A/C			intron-variant	FANCD2	GRCh38.p7	3:10054212	GTGAGACTCTATCTC[A/C]AAATAAATAAATAAA	2177
rs34896340	in-del	-/G			intron-variant	FANCD2	GRCh38.p7	3:10064924	GTTTTGAATGTTCAT[-/G]GGGGAATTCCACAGC	2177
rs34896574	snp	G/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092874	TTTTTCTATTTTTTG[G/T]GGAAACAGGGTCTCA	2177
rs34909440	snp	C/T	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10028103	AAGAAATGGTCCTTG[C/T]TTCTCTTTACCACCC	2177
rs34914111	snp	A/G	0.0603597	0.1629	intron-variant	FANCD2	GRCh38.p7	3:10069029	AGACTTCAAATTATG[A/G]AACTACTAACAACAA	2177
rs34915180	snp	C/G	0.00914312	0.0669923	intron-variant	FANCD2	GRCh38.p7	3:10065122	GGCGAAACACTGTCT[C/G]TACTAAAAATACAAA	2177
rs34927374	snp	C/G	0.0141837	0.08301	intron-variant	FANCD2	GRCh38.p7	3:10046254	GAGACGGGGTTTCAC[C/G]GTGTTAGTCAGGATG	2177
rs34930341	snp	A/G	0.00199481	0.0315187	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098532	TGTATCAGGGCCACA[A/G]ACATCTCAGAAACCT	2177
rs34936017	snp	A/G	0.0125903	0.0783366	FANCD2	3	allele_origin=G(germline)/A(germline)	3:10039727	CTACTGCAGGACCTC[A/G]CCACCAAGATCATGC	2177
rs34941997	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10027672	GCACTTTGGGAGTCC[A/G]AGGCGGGCGGATTAT	2177
rs34964213	snp	C/T	0.5	0	missense	FANCD2	GRCh38.p7	3:10067240	GCCAGGAAACATCAC[C/T]TGAGATGAAGGGGAA	2177
rs34965509	snp	A/G	0.29789	0.24537	intron-variant	FANCD2	GRCh38.p7	3:10042108	TCACCATATTGTCCA[A/G]GCTGGTCTTGAACTC	2177
rs34966633	in-del	-/T	0.365853	0.221536	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10097989	TGAGCATTTATAAGG[-/T]TTTTTTTAGTTGTCT	2177
rs34981366	snp	A/G	0.0108105	0.0727212	intron-variant	FANCD2	GRCh38.p7	3:10048667	TGGAAAATGTTTATG[A/G]AAGCAAGTAAAGAAC	2177
rs34989998	snp	A/G	0.32699	0.23785	intron-variant	FANCD2	GRCh38.p7	3:10031497	ACAGAGCAAGACTCC[A/G]TTTCAAAAAAAAAAA	2177
rs35015252	snp	A/G	0.0121208	0.0768991	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087584	ATAAATCATGAGGTT[A/G]ATAAAGTAGGAAATA	2177
rs35017428	snp	A/G	0.331179	0.236453	intron-variant	FANCD2	GRCh38.p7	3:10036107	TTTTTTTTTTTTTTG[A/G]GTCAGAGTCTCCTTT	2177
rs35043882	snp	C/T	0.0121208	0.0768991	intron-variant	FANCD2	GRCh38.p7	3:10038115	CCTGCCTCAGCCCCC[C/T]GAGTAGCTGGGATTA	2177
rs35065342	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10041048	AACATACAAAAATTA[A/G]GTGGGCGTGGTGGTA	2177
rs35070534	in-del	-/T	0.347914	0.230028	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092442	TTTTCTCACTAGGCA[-/T]TTTTTTTTTTGTCTT	2177
rs35080865	in-del	-/A			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10095069	TTTGAGAGGCAAATT[-/A]AAGATGATTATCAGC	2177
rs35086642	in-del	-/T			intron-variant	FANCD2	GRCh38.p7	3:10030113	TTTTTTTTTTTTTTT[-/T]GAGATGGAGTTTGGC	2177
rs35096513	in-del	-/TG	0.332106	0.236133	intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10026978	GTGCTGAAGCCAGAC[-/TG]TCCGAGTTAGAATCC	2177
rs35104427	snp	C/T	0.0314385	0.121371	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087901	ATCCACCTGCCTCAG[C/T]CTCCCAAAGTGCTGG	2177
rs35105956	in-del	-/T			intron-variant	FANCD2	GRCh38.p7	3:10037717	CAAAAAATAGAAATA[-/T]TTATGTGCACATTAA	2177
rs35108101	snp	A/C	0.00795532	0.062565	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096614	ACTGTTTAACTCTTA[A/C]AGTTATGGTACATTA	2177
rs35110529	snp	C/T	0.000694582	0.0186228	missense	FANCD2	GRCh38.p7	3:10032949	GAATTATTCTTAAAA[C/T]GGGAGAGAGTCAGAA	2177
rs35134252	in-del	-/A	0.303187	0.244277	intron-variant	FANCD2	GRCh38.p7	3:10071126	CCAAGAATGATCGAT[-/A]AAAAAAAAAAAAGAA	2177
rs35139285	snp	C/T	0.0104709	0.0715948	utr-variant-5-prime, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10026407	CGTCATGGCGCGCCT[C/T]GGTGGCGTCAGAGCG	2177
rs35140296	snp	C/T	0.333491	0.235646	intron-variant	FANCD2	GRCh38.p7	3:10030035	CAAGTGATCCATCCA[C/T]CTCGGCCTCCCAAAG	2177
rs35148833	snp	A/C	0.294832	0.245947	intron-variant	FANCD2	GRCh38.p7	3:10075253	AGTGGCGCGGATCTC[A/C]ACTCACTGCAAGCTC	2177
rs35149829	snp	A/T	0.289424	0.246872	intron-variant	FANCD2	GRCh38.p7	3:10062502	CTGCCTCGGCCTCCC[A/T]AAGTGCTGGGAGTAC	2177
rs35167719	snp	G/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10043697	CAAAACTCATTCAAG[G/T]GGAAATGATAGCTGA	2177
rs35173688	snp	A/C/G	0.0117288	0.0756758	FANCD2	3	allele_origin=G(germline)/A(germline)	3:10039303	TGATGAAATCAACAT[A/C/G]CCTCGACTCATTGTC	2177
rs35183009	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10029583	TCTTGATTTGTGTTG[G/T]TTTGTTTTTATTTTA	2177
rs35192086	in-del	-/G			intron-variant	FANCD2	GRCh38.p7	3:10056234	CATTGATGGACACTT[-/G]GGGTTGTTTCCACCT	2177
rs35193583	snp	A/T	0.00636936	0.0560724	intron-variant	FANCD2	GRCh38.p7	3:10031265	TCCCAGCACTTTGGG[A/T]GGCCAAGGCGGGCAG	2177
rs35196855	in-del	-/C			intron-variant	FANCD2	GRCh38.p7	3:10074521	TTGTTGCTGTGACTT[-/C]CCCCATAGGAGTTCA	2177
rs35198209	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10057452	TCACTCCAACCTCCG[C/G]CTCCCAGGTTCAAGT	2177
rs35198334	snp	C/G	0.290718	0.246662	intron-variant	FANCD2	GRCh38.p7	3:10062869	TTTGTATTTTTAGTA[C/G]AGACGGGGTTTCACC	2177
rs35204141	snp	A/C	0.0174175	0.0916809	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088044	AAAAATGCAAAACAA[A/C]CCTTTATTTATCCCT	2177
rs35208474	snp	C/T	0.308166	0.243139	intron-variant	FANCD2	GRCh38.p7	3:10046332	TGCTGGGATTACAGA[C/T]GTGAGCCACTGTGCC	2177
rs35209620	snp	G/T	0.00636936	0.0560724	intron-variant	FANCD2	GRCh38.p7	3:10031357	AACTACAAAAAATTA[G/T]CCGGGCGTGGTGGTG	2177
rs35213033	snp	C/T	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10075284	TGCCTCCCGGGTTCA[C/T]GCCATTCTGCTGCCT	2177
rs35220123	snp	C/T	0.29789	0.24537	intron-variant	FANCD2	GRCh38.p7	3:10041485	CAATTTTTAAAGAAA[C/T]ATACTATAAACGGTA	2177
rs35238230	snp	A/G	0.0108105	0.0727212	intron-variant	FANCD2	GRCh38.p7	3:10075277	CAAGCTCTGCCTCCC[A/G]GGTTCACGCCATTCT	2177
rs35247345	snp	A/C/G	0.0170603	0.0910578	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10091907	AGACTAGCCTGGCCA[A/C/G]CATGGTCAGTATATG	2177
rs35249095	snp	A/G	0.327741	0.237605	intron-variant	FANCD2	GRCh38.p7	3:10049225	AATCTCCTGAAGCCA[A/G]CATTAATGAAAACTA	2177
rs35268843	snp	C/T	0.00478085	0.0486577	intron-variant	FANCD2	GRCh38.p7	3:10035482	TTCCTGTTCTTAAAG[C/T]TGCATCCTGTGTATC	2177
rs35274744	snp	C/T	0.0322114	0.122752	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087678	TTTGAGACAGAGTCT[C/T]GTTCTGTCACCCAGG	2177
rs35293461	snp	A/G	0.381891	0.212379	intron-variant	FANCD2	GRCh38.p7	3:10048673	ATGTTTATGAAAGCA[A/G]GTAAAGAACAGTGTC	2177
rs35329575	snp	C/T	0.0137924	0.0818901	intron-variant	FANCD2	GRCh38.p7	3:10046262	GTTTCACCGTGTTAG[C/T]CAGGATGGTCTCGAT	2177
rs35345250	snp	G/T	0.000661835	0.0181791	intron-variant	FANCD2	GRCh38.p7	3:10052366	CTGCTAGCCTCATTG[G/T]TGGCATCATTTTTTC	2177
rs35348576	in-del	-/C			intron-variant	FANCD2	GRCh38.p7	3:10060113	AGAGGTTGCAGTGAG[-/C]CCGAGATTGCCCCTT	2177
rs35403996	snp	C/G	0.0418186	0.138422	intron-variant	FANCD2	GRCh38.p7	3:10073475	TAGGAAACAGCGAGC[C/G]AAAACTCTCTTAGGC	2177
rs35414488	snp	A/G	0.295854	0.245759	intron-variant	FANCD2	GRCh38.p7	3:10030826	AATTGCTTGAACCCC[A/G]GAGGTGGAGGTTGCA	2177
rs35431489	snp	G/T	0.0416478	0.138164	intron-variant	FANCD2	GRCh38.p7	3:10065711	GTTATATTTGTTGAT[G/T]GCTATATGATATGCA	2177
rs35435971	in-del	-/GG	0.00178192	0.0297957	intron-variant	FANCD2	GRCh38.p7	3:10046536	TAGCAAATGTACTGA[-/GG]TTTGTTAACTGTTTT	2177
rs35438680	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10075420	TCGATCTCCTGACCT[C/T]GTGATCACCCGCCTT	2177
rs35441595	snp	A/G	0.00953873	0.0683987	intron-variant	FANCD2	GRCh38.p7	3:10040121	CTCACTGCAACCTCC[A/G]CCTCCTGGGTTCACC	2177
rs35445187	snp	A/G	0.0279526	0.114869	intron-variant	FANCD2	GRCh38.p7	3:10052666	TGGGACTACAGGCAC[A/G]TGCCACCATACCCAG	2177
rs35474341	snp	A/C	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093084	AATCAGTTTATTTCT[A/C]TTTGCTCGTCTCTTC	2177
rs35480284	snp	C/G/T	0.000798403	0.0199641	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10081682	CCATTTGACAGATTA[C/G/T]GTGACTTGCTGATGA	2177
rs35480406	snp	C/T	0.00199481	0.0315187	intron-variant	FANCD2	GRCh38.p7	3:10031330	AACATGGTGAAACCC[C/T]GTCTCTACTAAAACT	2177
rs35481654	snp	C/T	0.0104709	0.0715948	utr-variant-5-prime, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10026472	GCGGCGACGGCTTCT[C/T]GGTGAGTAAGTGGAG	2177
rs35485751	snp	C/T	0.00159617	0.0282053	upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10025987	ACAACGCCTGCACTT[C/T]CTTGTCCAAGGTCAC	2177
rs35489304	snp	C/G	0.0104709	0.0715948	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096963	CTTGAGAAATAAAGG[C/G]ACAGAGTACAAAAGA	2177
rs35490742	snp	A/G	0.0314385	0.121371	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10089454	TAATATATTTGAGAG[A/G]ACCATGGTGGTTTTT	2177
rs35495399	snp	G/T	0.0431173	0.140355	FANCD2	3	allele_origin=G(germline)/T(germline)	3:10073349	CGCCATCTCATAGAG[G/T]CCAGCTAAACAAGGT	2177
rs35497255	snp	C/T	0.0146672	0.084371	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10089420	AGTCTGTTATGCATT[C/T]CTTTCAAGGGCTCTC	2177
rs35503714	snp	G/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088599	TCTATTTTGCTACTG[G/T]TGTTTGTCAGAGACT	2177
rs35513300	snp	A/G	0.0755793	0.179102	intron-variant	FANCD2	GRCh38.p7	3:10061891	TACCAAACACCGCAT[A/G]TTCTCACTCATAGGT	2177
rs35515831	snp	A/G	0.333491	0.235646	intron-variant	FANCD2	GRCh38.p7	3:10029678	AATTTTGGTGCACCT[A/G]TCACCCGAAAAGTGT	2177
rs35523931	snp	C/T	0.0134861	0.0810011	intron-variant	FANCD2	GRCh38.p7	3:10066182	ATTCACTTCACATTG[C/T]CCATGCTTTATTTTC	2177
rs35528998	snp	C/T	0.0314385	0.121371	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094641	GCACTCTCAGGTCCT[C/T]ATGTATCAGTGTGTC	2177
rs35546777	snp	A/G	0.0638572	0.166886	missense	FANCD2	GRCh38.p7	3:10072970	CAAAAATCAGAAAGA[A/G]AGGAAAAATAGGTAA	2177
rs35557429	snp	C/T	0.133448	0.221169	intron-variant	FANCD2	GRCh38.p7	3:10049365	TTCTGTTGACTCTCC[C/T]CTGTATAGGAAGTGG	2177
rs35561623	in-del	-/G			intron-variant	FANCD2	GRCh38.p7	3:10051484	GAGGCTATTGGCTTT[-/G]GGCAATTAGGATACC	2177
rs35563860	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10041925	TTTTTTTGAGACGGA[A/G]TATCACTCTGTCACC	2177
rs35568585	snp	A/G	0.00604385	0.0546388	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101157	AGAGCAGTAACCTAA[A/G]ATGCTTATTTATTTA	2177
rs35575700	snp	C/T	0.00636936	0.0560724	intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10027490	TTCCCCCACCTCTGC[C/T]GTCTGATTTCTAACT	2177
rs35585404	snp	C/T	0.0607341	0.163335	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10082239	GCTCTCCACCGTCTT[C/T]TTCCCACATCTGATT	2177
rs35586456	snp	A/G	0.334182	0.235401	intron-variant	FANCD2	GRCh38.p7	3:10075254	GTGGCGCGGATCTCC[A/G]CTCACTGCAAGCTCT	2177
rs35589432	snp	C/T	0.0193772	0.0965046	intron-variant	FANCD2	GRCh38.p7	3:10041987	AACTGCAACCTCTAC[C/T]TACCAAGTTCAAGCA	2177
rs35590470	snp	A/G	0.26271	0.249677	intron-variant	FANCD2	GRCh38.p7	3:10031489	CCTGGGCGACAGAGC[A/G]AGACTCCATTTCAAA	2177
rs35594075	snp	C/T	0.0178507	0.0927724	synonymous-codon	FANCD2	GRCh38.p7	3:10073359	TAGAGGCCAGCTAAA[C/T]AAGGTATTGGAATGA	2177
rs35619439	snp	A/G	0.00119737	0.0244387	intron-variant, utr-variant-3-prime	FANCD2, FANCD2OS	GRCh38.p7	3:10099291	CTTACGCTTTTTTGT[A/G]GTACAGATGCTTTCG	2177
rs35625434	snp	A/G	0.0078644	0.0622121	FANCD2	3	allele_origin=G(germline)/A(germline)	3:10043144	TGAAAAGTAAAGGAC[A/G]AGCAAGGTAAAGAGC	2177
rs35643728	in-del	-/A			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10089768	CATTGTGCCCAGCTG[-/A]AGATATTTTAGCCAT	2177
rs35650217	snp	A/G	0.00438332	0.0466095	intron-variant	FANCD2	GRCh38.p7	3:10031419	AGGCAGGAGAATGGC[A/G]TGAACCCGGGAGGCG	2177
rs35664310	in-del	-/T	0.0112991	0.0743093	intron-variant	FANCD2	GRCh38.p7	3:10032553	TTCAAGTGATCCTCC[-/T]GCCTTGGCCTCCTAA	2177
rs35668731	snp	A/G	0.0414363	0.137845	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10086146	TGAATGCATCAGCCC[A/G]TAAACTCAGCCTTTT	2177
rs35670565	snp	A/G	0.340265	0.233136	intron-variant	FANCD2	GRCh38.p7	3:10048940	TAGAGACACTGTCAT[A/G]ATCCATGTTTGCTTG	2177
rs35674884	in-del	-/C			intron-variant	FANCD2	GRCh38.p7	3:10051876	CAAAGTAAATAGTTT[-/C]CCTTGTGACTCCTTC	2177
rs35678855	snp	A/G	0.00343888	0.0413233	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094389	AGAGCAGAGAACAAA[A/G]ATATGCACTGAAGAG	2177
rs35700074	snp	A/G	0.0123036	0.0774623	intron-variant	FANCD2	GRCh38.p7	3:10062901	TGTTGGGGTTTCGCT[A/G]TGTTGACCAGGCTGG	2177
rs35711405	snp	C/T	0.295343	0.245854	intron-variant	FANCD2	GRCh38.p7	3:10075255	TGGCGCGGATCTCCA[C/T]TCACTGCAAGCTCTG	2177
rs35721602	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10036445	AAAGTCATATTTATC[A/G]TTATATTTCTTAAGT	2177
rs35723639	snp	C/T	0.0603597	0.1629	intron-variant	FANCD2	GRCh38.p7	3:10048460	AGGCACACACCACCA[C/T]GCCCGGTTAATTTTT	2177
rs35730671	snp	C/T	0.00557542	0.0525036	intron-variant	FANCD2	GRCh38.p7	3:10053392	TGGGGTGGGGGGAGG[C/T]GGGAGGGATAGCATT	2177
rs35734930	snp	A/G	0.00557542	0.0525036	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10097534	GGTTCTGTTCCGCCC[A/G]GCTCACCGGCGGTCA	2177
rs35741213	snp	A/G	0.298651	0.24522	intron-variant	FANCD2	GRCh38.p7	3:10045977	TTGGCAAGTGATTGA[A/G]TCTTTCTTTTAATAA	2177
rs35744325	snp	G/T	0.0607341	0.163335	intron-variant	FANCD2	GRCh38.p7	3:10046516	GGAAAAGCTGCTGTT[G/T]CATTGTAGCAAATGT	2177
rs35749514	snp	A/G	0.0173474	0.0915027	intron-variant	FANCD2	GRCh38.p7	3:10039690	TATTCTGGGTAATGT[A/G]CTGCAGTTCTAATAG	2177
rs35760922	in-del	-/A			intron-variant	FANCD2	GRCh38.p7	3:10051381	GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA	2177
rs35770561	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10086132	ATGCTAAATCTTCAT[A/G]AATGCATCAGCCCAT	2177
rs35771188	snp	C/G	0.00597247	0.0543191	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092416	CATCCTGGATAACCC[C/G]TTTTCTCACTAGGCA	2177
rs35775868	snp	A/G	0.0562307	0.157967	intron-variant	FANCD2	GRCh38.p7	3:10039947	TCTCTTCTATCTAAA[A/G]AGAGGATGATACCCC	2177
rs35777355	snp	A/C			intron-variant	FANCD2	GRCh38.p7	3:10054153	GGAAGTTGAGGCTAC[A/C]GTAAGCCATGTTTGT	2177
rs35782247	snp	G/T	0.0173266	0.09145	FANCD2	3	allele_origin=G(germline)/T(germline)	3:10048005	TTTCATTTGGCAGTC[G/T]CCTATACAAATATGC	2177
rs35784207	in-del	-/T	0	0	intron-variant	FANCD2	GRCh38.p7	3:10033708	TTTTTTTTTTTTTTT[-/T]GAGACGGAGTCTTGC	2177
rs35793548	snp	C/T	0.0607341	0.163335	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10082149	AGCATGCTCCTTCAG[C/T]TTTGCCTGGCTTAGT	2177
rs35805444	in-del	-/G			intron-variant	FANCD2	GRCh38.p7	3:10052660	GTGGCTGGGACTACA[-/G]GGCACGTGCCACCAT	2177
rs35817402	snp	C/T	8.23608e-05	0.00641667	synonymous-codon	FANCD2	GRCh38.p7	3:10065463	GGAGAGACAGCATAA[C/T]GGAAACTTGGAGGAG	2177
rs35818818	snp	G/T	0.0109286	0.0731087	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096300	GATAAACTCACAAAA[G/T]ATGGATGTTATTTAT	2177
rs35819769	snp	A/C	0.332799	0.23589	intron-variant	FANCD2	GRCh38.p7	3:10033990	GCATGAGCCACCGCG[A/C]CCAGCCAAAGCTAAG	2177
rs35821330	in-del	-/GT			intron-variant	FANCD2	GRCh38.p7	3:10054369	TATATATATATATAC[-/GT]GTATATACATATATA	2177
rs35835698	in-del	-/TCA	0.00358779	0.0422022	upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10025886	GTTATTATCCCCATT[-/TCA]TCACAGAGGACAAAA	2177
rs35844573	in-del	-/A	0.00478085	0.0486577	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10095449	TTGGGCAGTCCTCTA[-/A]GAGGGGAATCTCCGC	2177
rs35848502	snp	A/G	0.00636936	0.0560724	intron-variant	FANCD2	GRCh38.p7	3:10031369	TTAGCCGGGCGTGGT[A/G]GTGTGCACCTGTAGT	2177
rs35857570	snp	A/C	0.0104709	0.0715948	intron-variant	FANCD2	GRCh38.p7	3:10034943	ACTAAGTTTAAAATT[A/C]CTAAGCTTGTGGTTA	2177
rs35868820	snp	C/T	0.0106949	0.0723399	intron-variant	FANCD2	GRCh38.p7	3:10062443	GACGAGGTTTCACCA[C/T]GTTGGCCCCGCTGGT	2177
rs35870071	snp	G/T	0.341797	0.232537	intron-variant	FANCD2	GRCh38.p7	3:10043940	GCTTGCCTTCCCACT[G/T]TCTTTCTTTCTCCCC	2177
rs35870339	snp	C/T	0.0314385	0.121371	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088167	CAGCAGCATTCCTTT[C/T]CTCTGTGTGTCTGTA	2177
rs35888164	snp	A/G	0.0923359	0.194016	intron-variant	FANCD2	GRCh38.p7	3:10067417	GACAAAGACACATCA[A/G]AAAAAGAAATCTCAG	2177
rs35898115	snp	C/T	0.00557542	0.0525036	intron-variant	FANCD2	GRCh38.p7	3:10029974	TATCTTTAGTAGAGA[C/T]GGGGTTTCACCATGC	2177
rs35898916	snp	A/G	0.0116955	0.0755709	intron-variant	FANCD2	GRCh38.p7	3:10030929	AGTTGTGAAGCTCCA[A/G]TGGTTGATTAGTAAT	2177
rs35947447	snp	A/G	0.0744748	0.178019	intron-variant	FANCD2	GRCh38.p7	3:10048548	GACCTCAGGTGAACC[A/G]CCTGCCTCAGCCTCT	2177
rs35954417	snp	C/T	0.0134861	0.0810011	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096709	TGATATAAACAATGC[C/T]TCAGACATAAAGGAG	2177
rs35956820	snp	C/T	0.33099	0.236518	intron-variant	FANCD2	GRCh38.p7	3:10049137	AAAATCAGGAGGGCT[C/T]AGGTAGAGCTCACTG	2177
rs35966961	snp	C/T	0.00676609	0.0577691	intron-variant	FANCD2	GRCh38.p7	3:10050101	GCTAAAGAGTTTCAA[C/T]TTTATTTTTTAGACA	2177
rs35972737	snp	C/T	0.0105817	0.0719645	intron-variant	FANCD2	GRCh38.p7	3:10053356	GCACAGGAAGGGGAA[C/T]ATCACACTCTGGGGA	2177
rs35988239	snp	G/T	0.242775	0.249896	intron-variant	FANCD2	GRCh38.p7	3:10032461	AGTTTGTGTGTGGAG[G/T]GGGGGAATGGGGGTG	2177
rs35993975	snp	A/G	0.224709	0.248717	upstream-variant-2KB, nc-transcript-variant	FANCD2, CIDECP	GRCh38.p7	3:10026110	ACGTAGTGGCGGATC[A/G]TGTCTACGAAGAGTG	2177
rs36009699	in-del	-/T	0.00874735	0.0655527	intron-variant	FANCD2	GRCh38.p7	3:10061599	GAGAACATTAAAGGG[-/T]TTAGAACAATGTTTA	2177
rs36014300	snp	A/G	0.295088	0.245901	intron-variant	FANCD2	GRCh38.p7	3:10048565	CTGCCTCAGCCTCTC[A/G]AAGTGCTGGGATTAT	2177
rs36025301	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10057450	GCTCACTCCAACCTC[C/T]GCCTCCCAGGTTCAA	2177
rs36028199	in-del	-/AA			intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10028068	AACCCTGTCTCTACT[-/AA]AAAAAAAAAAAAAAA	2177
rs36037541	snp	A/G	0.0283406	0.115616	intron-variant	FANCD2	GRCh38.p7	3:10057639	AAGTGCTGTGATTAC[A/G]GGCATGAGCTACTGC	2177
rs36042034	snp	C/T	0.00676609	0.0577691	intron-variant	FANCD2	GRCh38.p7	3:10052306	TCTATGTGTGTCTCT[C/T]TTACAGGGATTTTAA	2177
rs36044753	in-del	-/A			intron-variant	FANCD2	GRCh38.p7	3:10064598	AGCTCCAAAATTCCT[-/A]AAAGGTTCACTGTTT	2177
rs36046453	in-del	-/T			intron-variant	FANCD2	GRCh38.p7	3:10078001	TCTTGCCACTGCACA[-/T]TTAACAAAAAAGAAA	2177
rs36051635	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10040571	AGTCCTGCATCAGAC[C/T]GCTTGCGGAGACCCA	2177
rs36052469	snp	A/G	0.00318978	0.0398085	intron-variant	FANCD2	GRCh38.p7	3:10065268	CACTCCAGACTGGGC[A/G]ACAGAGCAAGACTCT	2177
rs36066500	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10043665	TGTATAACTGAGGTA[A/G]ACTGAAATAAAAATC	2177
rs36072588	snp	C/T	0.00199481	0.0315187	intron-variant	FANCD2	GRCh38.p7	3:10057802	AATTAAAAAAAACAG[C/T]ATATTCATTTAACCA	2177
rs36075953	snp	A/T	0.0140615	0.0826621	intron-variant	FANCD2	GRCh38.p7	3:10073213	TTGGCAAACATGATT[A/T]TTAATTACTTGAGTC	2177
rs36080989	snp	C/T	0.00197912	0.031395	intron-variant	FANCD2	GRCh38.p7	3:10043197	AATTTTCTGACATCC[C/T]ACTGTCAGAGTTAGA	2177
rs36084488	snp	A/C/G	0.00608284	0.0548133	FANCD2	3	allele_origin=G(germline)/C(germline)	3:10032962	AACGGGAGAGAGTCA[A/C/G]AATCAACTAGGTAAT	2177
rs36086483	snp	A/C			intron-variant	FANCD2	GRCh38.p7	3:10054330	ACTGTGACTTTGAAC[A/C]ACCAGCATATATATA	2177
rs36091875	snp	A/T			intron-variant	FANCD2	GRCh38.p7	3:10054233	AATAAATAAATAAAT[A/T]AAACGAAGAGATTAG	2177
rs36103262	snp	A/C	0.00636936	0.0560724	intron-variant	FANCD2	GRCh38.p7	3:10060733	TATAGGCACTAGACA[A/C]TGCAGGTGTCTACAT	2177
rs36116894	snp	C/T	0.00636936	0.0560724	intron-variant	FANCD2	GRCh38.p7	3:10052049	GAGAACTGGGAGGTG[C/T]ATTAGAATGACTAAG	2177
rs36211699	in-del	-/TATATACATG			intron-variant	FANCD2	GRCh38.p7	3:10054420	ATATACGTATATACA[-/TATATACATG]TATATACATGTATAT	2177
rs41291203	snp	A/G	3.34146e-05	0.00408732	missense	FANCD2	GRCh38.p7	3:10039308	AAATCAACATACCTC[A/G]ACTCATTGTCAGTCA	2177
rs45510294	snp	A/C	0.00114264	0.023875	missense	FANCD2	GRCh38.p7	3:10032845	AGAAACCAGGAAGCA[A/C]CCACTTTCCAAAAAG	2177
rs45573142	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10091914	CCTGGCCAACATGGT[C/T]AGTATATGTTGCAAA	2177
rs45593431	snp	C/T	8.85857e-05	0.0066547	intron-variant	FANCD2	GRCh38.p7	3:10034815	TGTGGAGAGGAGGCA[C/T]GGAATCTTGCTGAAA	2177
rs45622438	snp	C/T	0.014617	0.0842308	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10081061	TTTCTGAGACGCTAT[C/T]CAGCAGTTTCTTCAC	2177
rs55663440	snp	A/C			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10095780	TGAACACAGAACCCT[A/C]GAGTTCTGCAGTCAC	2177
rs55682812	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10091860	AGCACTTTGGGAGGC[C/T]GAGGTGGGTGGATCA	2177
rs55716118	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090735	AGTGCTGAGATTACA[A/G]ACGTGCGCCACTGCG	2177
rs55719769	in-del	-/TTT/TTTT	0	0	intron-variant	FANCD2	GRCh38.p7	3:10054501	TTTTTTTTTTTTTTT[-/TTT/TTTT]GAGATGGAGTCTCGC	2177
rs55724940	snp	C/T	0.228547	0.249078	intron-variant	FANCD2	GRCh38.p7	3:10050495	GGGCATCGTGGCGGT[C/T]GCCTGTAGTCCCAGC	2177
rs55736797	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10086073	TGAGCTTTCTCATCT[A/G]TGTATTCTGATAAAT	2177
rs55741606	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10046873	AATTGTCTATCTCAA[G/T]GCAGTTTGCAACTTT	2177
rs55766724	snp	C/T	0.0611083	0.163768	intron-variant	FANCD2	GRCh38.p7	3:10056592	GCTGCAGTGCAGTGG[C/T]GTGATCATACTTCAC	2177
rs55774491	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093974	TTACCCAGTTTTTCC[C/T]TCTTGGGAGTAAGTT	2177
rs55789830	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10064160	TATCTGTCTGAGAGC[C/T]CTATTCTGTGCTGGG	2177
rs55804542	snp	C/T	0.00106638	0.0230663	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088562	GATGTTTGGTTTCTT[C/T]CAATGAGCCAAATAG	2177
rs55804747	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10064664	AATTGGTTTGCTCTA[C/G]TGGTTTTCCCTGTAG	2177
rs55817207	snp	A/G			intron-variant, utr-variant-5-prime, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10026543	TAATCTCTAAGTCCG[A/G]GCCGCGGTCGGCGTT	2177
rs55822690	snp	A/G	0.314544	0.241524	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10086319	GACCTTATGTGGCTG[A/G]GGGGTAGGCAGTGGA	2177
rs55829328	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10042358	TCACATTTATTGCCC[A/G]TCTATTTTTGATGAA	2177
rs55830075	snp	A/T			intron-variant	FANCD2	GRCh38.p7	3:10078801	AAACCCCATCTCTAC[A/T]AAAAATACAAAAAGA	2177
rs55839320	snp	C/T	0.0189856	0.0955633	intron-variant	FANCD2	GRCh38.p7	3:10046288	TCGATCTCCTGACCT[C/T]GTGATCTGCCCGCCT	2177
rs55856815	snp	C/G	0.0204165	0.0989516	synonymous-codon	FANCD2	GRCh38.p7	3:10064855	TGGGGGTCCGGTGAC[C/G]TCACAGGAATCAGGC	2177
rs55861393	in-del	-/GGCTAATCTCTA			intron-variant	FANCD2	GRCh38.p7	3:10049676	ACAGGCTAATCTCTA[-/GGCTAATCTCTA]TTCTGGGTGCTGTGA	2177
rs55861547	snp	C/G/T	3.29512e-05	0.00405891	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085889	GCCGACTGAAACAGG[C/G/T]AGAACACAGCCAGCC	2177
rs55863920	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10073170	TCTAGGCAGTTTCCA[A/G]CAGGTTGTTTTCTGA	2177
rs55882090	snp	C/T	0.366473	0.221211	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10097398	AGAGACAGGTACACC[C/T]GGGGGGGCCCAGTTC	2177
rs55891340	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090504	TTGTTCTGTTGCCCA[A/G]ACTGGAGTGCAGTGG	2177
rs55892753	snp	C/T	0.0103295	0.0711199	intron-variant	FANCD2	GRCh38.p7	3:10028913	TAACTTTGAGTATGA[C/T]CACAGCCTCTGGACC	2177
rs55895921	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10028404	TTATCCTTCAGCAAC[A/G]GCGAAGTAGTCTGCC	2177
rs55914626	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10095753	ATGAGGTATTGTCAC[A/G]TTTTGTCTGAATGAA	2177
rs55921165	snp	A/G	0.00504578	0.0499743	intron-variant	FANCD2	GRCh38.p7	3:10042712	GCAACTTAAGTGCCA[A/G]TTGCTCTTCTCTGTC	2177
rs55926585	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10042757	GAATACTGACTAATC[C/T]GGATAGCATTCAGAG	2177
rs55932659	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10034641	AGAATGATTTTTAAC[A/G]GCAAATATTAAACTA	2177
rs55951275	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094032	TATGCTCTCACTCCT[A/G]AGCTGAGCAAGTTCC	2177
rs55951691	in-del	-/G	0	0	intron-variant	FANCD2	GRCh38.p7	3:10051466	AAAGTTGAAGATGGA[-/G]GCAGAGGCTATTGGC	2177
rs55963803	snp	G/T	0.00318978	0.0398085	intron-variant, utr-variant-5-prime, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10026618	CCTGAGATGGGATAA[G/T]CCCCACAGGTACCTT	2177
rs55965714	snp	C/T	0.0119091	0.0762411	intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10026842	CTGATAATGGTTATC[C/T]GTATTAACCGAAGCG	2177
rs55973240	in-del	-/TT	0.333929	0.235491	intron-variant	FANCD2	GRCh38.p7	3:10035159	TGGAAAACAGATTTC[-/TT]TTTTTTTTACAGTAT	2177
rs55975672	snp	A/G	0.00199481	0.0315187	intron-variant	FANCD2	GRCh38.p7	3:10028443	TAACTAAGACTTGAA[A/G]GGAAGGTAGTATTGG	2177
rs55980657	snp	A/G	0.00536458	0.0515122	synonymous-codon	FANCD2	GRCh38.p7	3:10067307	AATAATCCTGGAAAA[A/G]TACTTGGCAGGTAAG	2177
rs55982342	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10049700	GCTGTGAATGTAAAG[G/T]AGGCCCTTACCTTTC	2177
rs55989944	snp	A/G	0.0314385	0.121371	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10085541	GGACTACAGGTGCCC[A/G]CCACCACACCCAGCT	2177
rs55990405	in-del	-/T			intron-variant	FANCD2	GRCh38.p7	3:10039431	GGTTGTATTTTTTTT[-/T]CTTTCTAAACAGAAA	2177
rs55997008	snp	G/T	0.0603597	0.1629	intron-variant	FANCD2	GRCh38.p7	3:10056171	GGCGTGAGCCACTGC[G/T]CCCGGCCCCCATTCT	2177
rs56002714	snp	G/T	0.00716266	0.059414	intron-variant	FANCD2	GRCh38.p7	3:10032759	TTTTCCTCTCATGAT[G/T]ATTATTCCTGGGTTT	2177
rs56036549	snp	A/G	0.5	0	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090577	AATTCTCCTGCCTCA[A/G]ACTCCTGAATAGCTG	2177
rs56041034	snp	A/C	0.00411881	0.0451934	missense	FANCD2	GRCh38.p7	3:10073260	TATAAAAGAAAGGAA[A/C]CAAAAAACAGATGGC	2177
rs56044667	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10034901	AATTTCATTTTTGGT[A/G]TAAGCTCTGTTTTCC	2177
rs56048698	snp	C/G	0.0023933	0.0345097	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10082605	CTATATAGCTTTTAC[C/G]TGGGAGGCTTTGCAC	2177
rs56048825	snp	C/G	0.0103295	0.0711199	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10086145	ATGAATGCATCAGCC[C/G]ATAAACTCAGCCTTT	2177
rs56061908	snp	A/G	0.00914312	0.0669923	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094112	TTAGTTAACAGGCCT[A/G]TTTGATTTTTGTATT	2177
rs56070953	snp	A/G	0.0023933	0.0345097	upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10025961	CGAGACGTGAACCTA[A/G]GCAAACTGACACAAC	2177
rs56071305	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10052206	GTTTATATCCAGTCT[A/G]TCAAACCTTTGGGCT	2177
rs56077532	in-del	-/CTA			intron-variant	FANCD2	GRCh38.p7	3:10074936	CTACTACTACTACTA[-/CTA]ATAAGCTACCTAGAT	2177
rs56083801	snp	G/T	0.000461612	0.0151853	intron-variant	FANCD2	GRCh38.p7	3:10041605	TATACAACTTTTTTC[G/T]TTTTCTACCATTCAC	2177
rs56093431	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10040464	ACTTGTTCTTCAGGG[A/G]GTCCTTAACCCTGGC	2177
rs56096530	in-del	-/C	0	0	intron-variant	FANCD2	GRCh38.p7	3:10051432	GTGAGGGATTTATCT[-/C]CCAGTGTTGGACACT	2177
rs56098809	snp	A/G	0.00557542	0.0525036	intron-variant	FANCD2	GRCh38.p7	3:10028886	CTGAGTTTTTGCCTC[A/G]AATTCTGCGTATAAC	2177
rs56102803	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090728	CTCCCAAAGTGCTGA[A/G]ATTACAGACGTGCGC	2177
rs56123930	snp	A/G	0.0279526	0.114869	intron-variant	FANCD2	GRCh38.p7	3:10028869	AAATATCAGATTTGG[A/G]ACTGAGTTTTTGCCT	2177
rs56146486	snp	A/G	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10065184	ATCCCAGCTACTCAG[A/G]AGGCTGAGGCAGGAT	2177
rs56156755	snp	A/G	0.0162398	0.0886349	intron-variant	FANCD2	GRCh38.p7	3:10043223	TTAGAGCTTAATACT[A/G]CTACAAATAATGATA	2177
rs56162920	snp	C/T	0.00119737	0.0244387	utr-variant-5-prime, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10026416	GCGCCTCGGTGGCGT[C/T]AGAGCGGCGTCGGGC	2177
rs56169295	snp	C/T	0.0150606	0.0854603	intron-variant	FANCD2	GRCh38.p7	3:10065104	TTACTTTCTGGCCAA[C/T]GTGGCGAAACACTGT	2177
rs56176124	snp	C/G	0.0209421	0.100162	intron-variant	FANCD2	GRCh38.p7	3:10028868	GAAATATCAGATTTG[C/G]GACTGAGTTTTTGCC	2177
rs56219631	snp	A/G	0.0263992	0.111815	intron-variant	FANCD2	GRCh38.p7	3:10040651	AAGAAGGGGAGAACA[A/G]TATCCCTAGGTAATA	2177
rs56224827	snp	C/T	0.0103295	0.0711199	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10081035	GACTTGACTCCATTG[C/T]GAACCCTTAGTTTCT	2177
rs56238688	in-del	-/A			intron-variant	FANCD2	GRCh38.p7	3:10039993	TATGGGATTTGACTT[-/A]AAAAAAAAAGGTATA	2177
rs56238808	snp	A/T			intron-variant	FANCD2	GRCh38.p7	3:10054473	TATATATATATATAT[A/T]TTTTTTTTTTTTTTT	2177
rs56241637	snp	C/G	0.29789	0.24537	intron-variant	FANCD2	GRCh38.p7	3:10045852	TAATCCACCCATCTC[C/G]GCCTCCCAAAGTGCT	2177
rs56252804	snp	C/T	0.0107246	0.0724382	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10089141	AATACAAAAATTAGC[C/T]GGGCGTGGTGGCACA	2177
rs56262334	in-del	-/G			intron-variant	FANCD2	GRCh38.p7	3:10049307	GGAGAGGCCTTGGGG[-/G]TGAATCCCTTTAGAA	2177
rs56270432	snp	C/G	0.34303	0.232046	intron-variant	FANCD2	GRCh38.p7	3:10045833	TCTTGAACTCCTGAC[C/G]TCGTAATCCACCCAT	2177
rs56276708	snp	C/T	0.365232	0.22186	intron-variant	FANCD2	GRCh38.p7	3:10055770	TGAGCCGAGATCGCA[C/T]CACTGCACTCCAGCC	2177
rs56295307	in-del	-/G			intron-variant	FANCD2	GRCh38.p7	3:10051415	AAAAAAAACAAAAAG[-/G]AGTGAGGGATTTATC	2177
rs56314425	snp	C/T	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10074784	AGAAGTTAGACTGAC[C/T]TTTAAAGCCTTTATA	2177
rs56321271	in-del	-/T			intron-variant	FANCD2	GRCh38.p7	3:10028466	GTATTGGCTAGATGT[-/T]AAGAGTTGAAATTTG	2177
rs56339684	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10078776	CAAGACCAGCCTGGC[C/T]AACATGGTGAAACCC	2177
rs56350437	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10043722	AGCTGATGGTTGCCA[G/T]ATGGACACATTGGCT	2177
rs56402359	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10065517	ATGAAGTCATCAGAT[C/G]CTTTCTTCTTTATAC	2177
rs56402413	snp	A/C/G	0.000115376	0.00759447	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093350	ACTGGGCCCTGTTTC[A/C/G]TATTTATTCTTCCTG	2177
rs56405709	snp	C/G	3.30568e-05	0.00406538	missense	FANCD2	GRCh38.p7	3:10032908	AGAAAATGACAGCAT[C/G]TTTGTAAAGCTTCTT	2177
rs56720597	snp	A/T			intron-variant	FANCD2	GRCh38.p7	3:10078734	TTTGGGAGGCCAAGG[A/T]GGGCAGATCACTTGA	2177
rs56931017	in-del	-/TTTTTGTTTTTG			intron-variant	FANCD2	GRCh38.p7	3:10045187	TTGTTTTTGTTTTTG[-/TTTTTGTTTTTG]AGACGGGTTCTCACT	2177
rs57198896	in-del	-/G			intron-variant	FANCD2	GRCh38.p7	3:10051414	AAAAAAAAACAAAAA[-/G]GAGTGAGGGATTTAT	2177
rs57434752	snp	A/C	0.0629771	0.165899	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10083187	AGCCAAGATTGCAAC[A/C]CTGCACTCCAACCTG	2177
rs57631744	snp	C/G/T	0.494168	0.23205	intron-variant	FANCD2	GRCh38.p7	3:10077278	AATTATTTACCCTGC[C/G/T]GGGCGCAGTGGCTCA	2177
rs57661428	in-del	-/TTTTTTTTTTTT			intron-variant	FANCD2	GRCh38.p7	3:10046070	TTTTTTTTTTTTTTT[-/TTTTTTTTTTTT]GAGAATGGAATCTCG	2177
rs57693909	in-del	-/T			intron-variant	FANCD2	GRCh38.p7	3:10075200	TTCTTTTTTTTTTTT[-/T]GAGATGGAGTCTCTC	2177
rs57788422	snp	A/C	0.333491	0.235646	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10083866	GCACTCCAGCCTGGG[A/C]GACAGAGCAAGACTC	2177
rs58265237	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10100528	AGGTGCCTGCAACCA[C/T]GCCCGGCTAGTTTTT	2177
rs58275763	snp	C/T	0.309894	0.242719	utr-variant-3-prime, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101590	GGGGTTTTACCATGT[C/T]GGCCAGATGGTCTCA	2177
rs58316932	in-del	-/A			intron-variant	FANCD2	GRCh38.p7	3:10050643	AAAAAAAAAAAAAAA[-/A]GGCTTAGAAGAGCAC	2177
rs58380785	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10078748	GAGGGCAGATCACTT[A/G]AGTTCAGGAGTTCAA	2177
rs58543053	snp	C/T	0.342582	0.232225	intron-variant	FANCD2	GRCh38.p7	3:10070275	GCCCGGCAGCCACCC[C/T]GTCTGGGAAGTGAGG	2177
rs58598088	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10100581	TTCACCATGTTGGCC[A/G]GGCTGGTCTCGAACT	2177
rs58896767	in-del	-/TT			intron-variant	FANCD2	GRCh38.p7	3:10076285	GTCTTTTTTTTTTTT[-/TT]CCCAAACCCTGTGTG	2177
rs59318799	snp	A/T	0.310878	0.242475	utr-variant-3-prime, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101644	TGCCTCAGCCTCCCA[A/T]AGTGCTGGGATTACA	2177
rs59403769	snp	A/C	0.212122	0.247114	intron-variant	FANCD2	GRCh38.p7	3:10068141	AAGTCCTAGCTAGAA[A/C]AATTAGACAAGAGAG	2177
rs60061292	snp	A/G	0.295599	0.245806	intron-variant	FANCD2	GRCh38.p7	3:10070180	GTGAGGAGACCCTCC[A/G]CCCGGCAACCGCCCC	2177
rs60206342	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10100538	AACCATGCCCGGCTA[A/G]TTTTTGTATATTTAG	2177
rs60370969	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10078751	GGCAGATCACTTGAG[G/T]TCAGGAGTTCAAGAC	2177
rs60393040	snp	A/C			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10100580	TTTCACCATGTTGGC[A/C]GGGCTGGTCTCGAAC	2177
rs60481412	snp	A/C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10100414	AGTCTCCCTCTGTCG[A/C/T]CCAGGCTAGCATGCA	2177
rs60546930	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10078739	GAGGCCAAGGAGGGC[A/G]GATCACTTGAGTTCA	2177
rs60829238	in-del	-/CCT			intron-variant	FANCD2	GRCh38.p7	3:10033809	GGTTCACACCATTCT[-/CCT]GCCTCAGCTTCCCAA	2177
rs60853982	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10078857	ATAGTTCCAGCTACT[C/T]GGGAGGCTGAGGCAT	2177
rs60979132	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10078781	CCAGCCTGGCCAACA[C/T]GGTGAAACCCCATCT	2177
rs61017294	snp	C/G	0.0558544	0.157504	intron-variant	FANCD2	GRCh38.p7	3:10056573	GTCTTATTCTGTTAC[C/G]CAAGCTGCAGTGCAG	2177
rs61077902	snp	G/T	0.313326	0.241847	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10084469	TGATTTTTCCTTTTT[G/T]TTTTCTTTGGTAGAG	2177
rs61213308	in-del	-/C			intron-variant	FANCD2	GRCh38.p7	3:10051408	AAAAAAAAAAAAAAA[-/C]AAAAAGGAGTGAGGG	2177
rs61438880	in-del	-/A	0.344815	0.231323	intron-variant	FANCD2	GRCh38.p7	3:10051083	AAGAGCGAAACTGTC[-/A]AAAAAAAAAGAGTGA	2177
rs61529210	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10100475	CTCCCGAGTTCAAGC[A/G]ATTCTCCTGCCTCAG	2177
rs61692836	snp	A/G	0.0755793	0.179102	intron-variant	FANCD2	GRCh38.p7	3:10072342	GGAGTGTGGTGGTGC[A/G]ATCTCTGCTTACTAC	2177
rs61740079	snp	C/T	0.0798611	0.183174	synonymous-codon	FANCD2	GRCh38.p7	3:10072905	TCCTCTTGGAAACTT[C/T]GATGTGGAAACTTTA	2177
rs61751576	snp	G/T			synonymous-codon	FANCD2	GRCh38.p7	3:10039771	TGCTCCAGAGAACCT[G/T]CAGCATGACATCATC	2177
rs61751577	snp	G/T	0.00023855	0.0109187	synonymous-codon	FANCD2	GRCh38.p7	3:10067241	CCAGGAAACATCACC[G/T]GAGATGAAGGGGAAG	2177
rs61751578	snp	A/C/G	0.000428297	0.0146277	missense	FANCD2	GRCh38.p7	3:10074617	ATTGAGGTCTTCTCT[A/C/G]TTCTACATTGTGGAC	2177
rs61753270	snp	C/G	0.000115427	0.00759606	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098767	GAGCACAGCAGATGA[C/G]AGTGAGGATGACATG	2177
rs62245504	snp	A/T	0	0	intron-variant	FANCD2	GRCh38.p7	3:10030097	TGGCCCATTATATCA[A/T]TTTTTTTTTTTTTTT	2177
rs62245505	snp	A/G	0.0142736	0.0832652	intron-variant	FANCD2	GRCh38.p7	3:10031230	GAAAGGAGGCCAGGC[A/G]CGGTGGCTCACGCCT	2177
rs62245506	snp	A/T	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10037092	CTCAAGTGGTCCACC[A/T]GCCTTAGCCTCTCAA	2177
rs62245507	snp	A/G	0.0444908	0.142359	intron-variant	FANCD2	GRCh38.p7	3:10045142	CTGAATACACGCCCA[A/G]TGTTTTCTCTTTTTT	2177
rs62245508	snp	A/G	0.493201	0.0579094	intron-variant	FANCD2	GRCh38.p7	3:10048054	GTACTGCCAGCAGGT[A/G]TGTTGAAACATTTAT	2177
rs62245509	snp	C/T	0.0498117	0.149749	intron-variant	FANCD2	GRCh38.p7	3:10050350	ATGTGGCGGTCCGGG[C/T]GCGGTGGCTCATGCT	2177
rs62245510	snp	C/T	0.0364509	0.129988	intron-variant	FANCD2	GRCh38.p7	3:10050362	GGGTGCGGTGGCTCA[C/T]GCTTGTAATCCCAGC	2177
rs62245511	snp	C/T	0.0463947	0.145069	intron-variant	FANCD2	GRCh38.p7	3:10050365	TGCGGTGGCTCATGC[C/T]TGTAATCCCAGCACT	2177
rs62245512	snp	A/T			intron-variant	FANCD2	GRCh38.p7	3:10052961	CAACCATTGTGGAAG[A/T]CAGTGTGGCGATTCC	2177
rs62245514	snp	A/C/G	0.0580493	0.160174	intron-variant	FANCD2	GRCh38.p7	3:10063755	TTGGGAAAGATTGGC[A/C/G]GCCCAAGGTTTAAAC	2177
rs62245515	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10064529	CTTCACCTCAGCCAC[A/G]GCTGCCCAGTCCCAC	2177
rs62245516	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10064580	CAGCACCCCTGCACC[C/T]TTAGCTCCAAAATTC	2177
rs62245518	snp	C/T	0.00636936	0.0560724	intron-variant	FANCD2	GRCh38.p7	3:10072670	TGATAATTGATCATA[C/T]TTAATATGATATTTC	2177
rs62245546	snp	C/T	2.37358e-05	0.0034449	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087280	GTGATGGGCCTAGAT[C/T]CTTTTTTTTTTTTTT	2177
rs66493421	snp	A/G	0.201727	0.245295	intron-variant	FANCD2	GRCh38.p7	3:10050885	TGAGGTTGGGAGTTC[A/G]AATCAGCCTGACCAA	2177
rs66543323	snp	A/G	0.29789	0.24537	intron-variant	FANCD2	GRCh38.p7	3:10044697	TTAGTTTTGTTATCC[A/G]ATTTTGGGATGATTA	2177
rs66797209	snp	A/G	0.29789	0.24537	intron-variant	FANCD2	GRCh38.p7	3:10036842	TACCTTTTAAATTTT[A/G]TAGTGTATGTTCAGA	2177
rs66798126	in-del	-/A	0.375	0.216506	intron-variant	FANCD2	GRCh38.p7	3:10030060	GTGGCTCAAGCCTGT[-/A]ATCCTTGCACTTTGG	2177
rs66915020	snp	A/G	0.32885	0.23724	intron-variant	FANCD2	GRCh38.p7	3:10068490	TTGATGCAAGAAATT[A/G]AAGAGCAAATAAAAA	2177
rs71052292	in-del	-/A/T			intron-variant	FANCD2	GRCh38.p7	3:10075748	TTTTTTTTTTTTTTT[-/A/T]GAGATGGAGTCTCGC	2177
rs71052293	in-del	-/A/T	6.26494e-05	0.0055965	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087300	TTAGTCCTATTCATT[-/A/T]AAAAAAAAAAAAAAA	2177
rs71314387	snp	C/G	0.00358779	0.0422022	intron-variant	FANCD2	GRCh38.p7	3:10044673	GGAATCTGTTTTGTG[C/G]GATTTTTGTTAGTTT	2177
rs71314388	snp	A/G	0.0146672	0.084371	intron-variant	FANCD2	GRCh38.p7	3:10077931	CCCCGCTACTCGGGA[A/G]GCTGAGATGGGAGGA	2177
rs71314389	snp	A/G	0.5	0	utr-variant-3-prime, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101570	TTTGTATTTTTAGTA[A/G]ATACGGGGTTTTACC	2177
rs71626957	in-del	-/G	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10033260	AAAAAATTAGCCGGG[-/G]CATGGTGGCATGTGC	2177
rs71626958	in-del	-/T	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10059041	TATTTTGAGACAATG[-/T]CTGGCTCTGTCACCC	2177
rs71626959	in-del	-/C	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10080744	CACTGCACTCCAGCC[-/C]TGGGTGACAGAGCAG	2177
rs72492715	in-del	-/AA			intron-variant	FANCD2	GRCh38.p7	3:10059821	AAAGAAAAAAAAAAA[-/AA]GTCCCCATTTCACAG	2177
rs72492997	snp	G/T	0.468497	0.121486	synonymous-codon	FANCD2	GRCh38.p7	3:10046582	TTATTGACAATAGGT[G/T]TTTGACCTGGTGATG	2177
rs72492998	snp	C/T	0.49106	0.0662561	synonymous-codon	FANCD2	GRCh38.p7	3:10046624	CTATAGCACCAATAC[C/T]CAGACAAAGAAGTAC	2177
rs72492999	snp	A/G	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10046898	AACTTTGACAAACTG[A/G]CCTTCCGTATCCTAT	2177
rs72493000	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10047349	ATTGCATTTTCCCCA[A/G]TAAAGCATTATACCC	2177
rs72493001	snp	A/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10047514	TCTTGATCTTCTTTT[A/T]AAAAAATCAGCTTAG	2177
rs73014597	snp	C/T	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10047192	CTAATGAGAATACCT[C/T]GCTGGGTCTTAAATT	2177
rs73014600	snp	C/T	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10047194	AATGAGAATACCTCG[C/T]TGGGTCTTAAATTTT	2177
rs73016506	snp	C/T	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10047525	TTTTAAAAAAATCAG[C/T]TTAGTTAGCATTGAA	2177
rs73016516	snp	C/T	0.0637235	0.166737	intron-variant	FANCD2	GRCh38.p7	3:10057064	TTTTGTCATGTTACC[C/T]AGACTGGTTTGGAAC	2177
rs73016531	snp	C/T	0.0166325	0.0896639	intron-variant	FANCD2	GRCh38.p7	3:10067827	AGAAAGATTATTCAT[C/T]ATGGCCAAATGGGAT	2177
rs73016558	snp	A/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10079815	CGGGGAAGCAGTTGG[A/T]CGGTACATATAACAA	2177
rs73016577	snp	C/T	0.0314385	0.121371	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10091385	TGCACCTGGCATAAA[C/T]CAGTGCAGCCCAGAA	2177
rs73126218	snp	A/G	0.487221	0.0789068	missense	FANCD2	GRCh38.p7	3:10046659	ACAGGGTGCTAAGAA[A/G]TAAGATTCGATCAGG	2177
rs73128264	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10073532	GTTCAGATTAGACTT[C/T]AGGTCCTTATTCCTG	2177
rs73811815	snp	A/G	0.0603597	0.1629	intron-variant	FANCD2	GRCh38.p7	3:10046872	TAATTGTCTATCTCA[A/G]TGCAGTTTGCAACTT	2177
rs73811818	snp	G/T	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10048202	CCAGCCTTGATGAAA[G/T]GAAGAGACTTGACTG	2177
rs74207582	snp	A/T	0.444444	0.157135	intron-variant	FANCD2	GRCh38.p7	3:10047391	AAATATAAGATTTTT[A/T]AAAATTATGGTATCA	2177
rs74341139	snp	A/G	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10046974	GAAACTAGTAGAAAT[A/G]TAAATATGTACCTAT	2177
rs74351786	snp	A/T	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10048150	ACTGAAGGGGAAGGA[A/T]CTCTGACCTGGGTCT	2177
rs74509181	snp	A/C	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10048157	GGGAAGGAACTCTGA[A/C]CTGGGTCTCAAGAAA	2177
rs74584011	snp	A/G	0.00676609	0.0577691	intron-variant	FANCD2	GRCh38.p7	3:10042240	GAGTGGAAATCTTCC[A/G]TGTTGTCTGAGTCAT	2177
rs74627529	snp	C/G	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10047624	AACTGGGATTTAGAA[C/G]ATCTGGCCTCCAATC	2177
rs74644901	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10082066	ATATCCAACTGCCTA[C/T]GCAACACCTCCTTAG	2177
rs74696761	snp	A/G	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10047594	ATCCCTGGGGGTAGT[A/G]TGATTGCATGGGGAA	2177
rs74734198	snp	C/T	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10047550	ATTGAACCTTATAGA[C/T]CTACTTCAAATTATA	2177
rs74742086	snp	G/T	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10047280	TTTATTTCTGCCAAT[G/T]ATACATGTTTTGGGC	2177
rs74748421	snp	G/T	0.5	0	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10095898	TTTTTTTTTTTTTTT[G/T]TGAGACGGAGTCTCG	2177
rs74803504	snp	A/G	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10047278	TGTTTATTTCTGCCA[A/G]TTATACATGTTTTGG	2177
rs74873878	snp	C/G	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10047068	TAAATTATTCAAAGT[C/G]GAATTTTATAAGCTA	2177
rs74882077	snp	A/G	0	0	intron-variant	FANCD2	GRCh38.p7	3:10059822	AAGAAAAAAAAAAAA[A/G]GTCCCCATTTCACAG	2177
rs74923817	snp	A/C/T	1.64825e-05	0.00287071	intron-variant	FANCD2	GRCh38.p7	3:10035170	TTTCTTTTTTTTTTA[A/C/T]AGTATGGGTGCATCT	2177
rs74925173	snp	A/G	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10048451	TGTGATTACAGGCAC[A/G]CACCACCACGCCCGG	2177
rs75087355	snp	A/C/G	0.000197785	0.0099425	intron-variant	FANCD2	GRCh38.p7	3:10035169	ATTTCTTTTTTTTTT[A/C/G]CAGTATGGGTGCATC	2177
rs75123690	snp	A/G	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10048449	GCTGTGATTACAGGC[A/G]CACACCACCACGCCC	2177
rs75205435	snp	A/G	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10047577	TATAACCAAGGTGGA[A/G]CATCCCTGGGGGTAG	2177
rs75274508	snp	A/G	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10048168	CTGACCTGGGTCTCA[A/G]GAAAGCTCAATTCTA	2177
rs75307634	snp	A/G	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10047156	CTGGATGGGCCAGTG[A/G]TTTGGGGTTTGGGTT	2177
rs75356275	snp	C/T	0.00318978	0.0398085	intron-variant	FANCD2	GRCh38.p7	3:10031237	GGCCAGGCACGGTGG[C/T]TCACGCCTGTAATCC	2177
rs75389047	snp	A/G	0.483936	0.0881695	intron-variant	FANCD2	GRCh38.p7	3:10048091	AAGGAGGGAACACAG[A/G]AAGGGAAAATAATCT	2177
rs75478634	in-del	-/TCA/TCG			upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10025889	ATTATCCCCATTTCA[-/TCA/TCG]CAGAGGACAAAAGTG	2177
rs75488127	snp	G/T	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10059823	AGAAAAAAAAAAAAA[G/T]TCCCCATTTCACAGA	2177
rs75492034	snp	A/T	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10047663	AGCAGATAGGAATGT[A/T]CTATTAGGCTTGTAA	2177
rs75494031	snp	A/G	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10073589	ATTATTTTCTTGACT[A/G]TTTTACTCCCTTTTT	2177
rs75639982	snp	A/G	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10047605	TAGTATGATTGCATG[A/G]GGAAACTGGGATTTA	2177
rs75659199	snp	C/T	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10048551	CTCAGGTGAACCGCC[C/T]GCCTCAGCCTCTCAA	2177
rs75667124	snp	A/G	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10047675	TGTTCTATTAGGCTT[A/G]TAATTTAACTTCTTT	2177
rs75735845	snp	A/G	0.0707826	0.174302	intron-variant	FANCD2	GRCh38.p7	3:10079569	TCGGCCTCCCAATCC[A/G]CCCACCTCGGCCTCC	2177
rs75749119	snp	G/T	0	0	intron-variant	FANCD2	GRCh38.p7	3:10036103	TTTTTTTTTTTTTTT[G/T]TTGAGTCAGAGTCTC	2177
rs75794111	snp	A/G	0.0566069	0.158427	intron-variant	FANCD2	GRCh38.p7	3:10041143	AAGCTACAGTGAGCT[A/G]TGATGACACCACTGT	2177
rs75828230	snp	A/G	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10047046	GGTGATAATTCCTCT[A/G]GAAATGTAAATTATT	2177
rs75982987	snp	C/G	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10048491	TGTATTTTTAGTAGA[C/G]ACAGCGTTTCACCAT	2177
rs75992391	snp	C/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10082506	AAACTCTCTTACCTA[C/G]CCTCTAGGTCTTCTT	2177
rs76034195	snp	A/G	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10047083	GGAATTTTATAAGCT[A/G]GGAATAGTGTTTTGC	2177
rs76041173	snp	G/T	0.297128	0.245518	intron-variant	FANCD2	GRCh38.p7	3:10037011	CAGCTAATTTTCGTG[G/T]TTTTTTTTTTTTTGG	2177
rs76052788	snp	C/T	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10047465	ATTAATGTCTATGTA[C/T]ATTGAATTATTGGTA	2177
rs76158484	snp	G/T	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10038598	TTTTTTTTTTTTTTT[G/T]AGACAGAGTCTTGGC	2177
rs76222773	snp	G/T	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10047483	TGAATTATTGGTAGG[G/T]TATGATCACTTCTCT	2177
rs76340293	in-del	-/TT			intron-variant	FANCD2	GRCh38.p7	3:10045100	ACTGTTTTTTTTTTT[-/TT]CCTGGAAGCATAGAC	2177
rs76349278	snp	A/G	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10048660	GTATTTGTGGAAAAT[A/G]TTTATGAAAGCAAGT	2177
rs76378341	snp	A/C	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10047470	TGTCTATGTACATTG[A/C]ATTATTGGTAGGTTA	2177
rs76489091	snp	C/T	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10047107	GTTTTGCCAGCTGAA[C/T]GTTCAGGATATTAGC	2177
rs76519400	snp	C/T	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10048604	GCCATTGGGCCTGGC[C/T]GAGACACATTTTAAT	2177
rs76640678	snp	C/T	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10047544	GTTAGCATTGAACCT[C/T]ATAGACCTACTTCAA	2177
rs76702750	snp	C/T	0.5	0	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087284	TGGGCCTAGATCCTT[C/T]TTTTTTTTTTTTTTT	2177
rs76714355	snp	C/T	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10047537	CAGCTTAGTTAGCAT[C/T]GAACCTTATAGACCT	2177
rs76721152	snp	G/T	0	0	intron-variant	FANCD2	GRCh38.p7	3:10079933	CTTCTTTTTTTTTTT[G/T]GAGGCGGAGTCTTGC	2177
rs76763819	snp	A/C	0.0554779	0.157039	intron-variant	FANCD2	GRCh38.p7	3:10057016	TGCACCACCATGCCC[A/C]GCTAATTTTTTATAA	2177
rs76772579	snp	G/T	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10047232	GGAATAGATTTAACG[G/T]TTGTATTATTTTATC	2177
rs76825922	snp	C/T	0	0	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087283	ATGGGCCTAGATCCT[C/T]TTTTTTTTTTTTTTT	2177
rs77015110	snp	A/T	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10046983	AGAAATGTAAATATG[A/T]ACCTATTTGAACTAT	2177
rs77076948	snp	A/C			intron-variant	FANCD2	GRCh38.p7	3:10049568	TGGGAGGTGGTGGGA[A/C]GGAGGTGARATGATG	2177
rs77099000	snp	C/T	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10047484	GAATTATTGGTAGGT[C/T]ATGATCACTTCTCTT	2177
rs77148318	snp	C/T	0.0150606	0.0854603	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10080831	CCTAAATGATTTCTA[C/T]TTTTATGTGACCTTT	2177
rs77169020	snp	A/C	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10048131	TTCTTGTTGGTTGGA[A/C]CTCACTGAAGGGGAA	2177
rs77192427	in-del	-/CC			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087280	GTGATGGGCCTAGAT[-/CC]TTTTTTTTTTTTTTT	2177
rs77210797	snp	A/G/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10047056	CCTCTAGAAATGTAA[A/G/T]TTATTCAAAGTGGAA	2177
rs77246387	snp	A/G	0.0858781	0.188584	synonymous-codon	FANCD2	GRCh38.p7	3:10067214	TACTTTGCAGATTGT[A/G]AATGCCTTCTGCCAG	2177
rs77263972	snp	A/G	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10048144	GAACTCACTGAAGGG[A/G]AAGGAACTCTGACCT	2177
rs77270659	snp	C/G	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10069460	ACCCTAGTTAAGATG[C/G]CTCTCCCCCTCCCCC	2177
rs77302521	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10047246	GGTTGTATTATTTTA[C/T]CTTGCAGTTCTTTCT	2177
rs77384918	snp	A/G	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10047274	TCTGTGTTTATTTCT[A/G]CCAATTATACATGTT	2177
rs77391196	snp	C/G	0.5	0	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090472	TTTTTTTTTTTTTTT[C/G]TGAGACAGAGTCTTG	2177
rs77441281	snp	C/T	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10047554	AACCTTATAGACCTA[C/T]TTCAAATTATAACCA	2177
rs77470126	snp	C/T	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10046973	AGAAACTAGTAGAAA[C/T]GTAAATATGTACCTA	2177
rs77520528	snp	A/G	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10047825	GAGCTAGGGAGGAGA[A/G]GTCTGACATTCCAAA	2177
rs77529198	snp	C/T	0	0	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090467	TTTTTTTTTTTTTTT[C/T]TTTTCTGAGACAGAG	2177
rs77580712	snp	A/G	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10046905	ACAAACTGGCCTTCC[A/G]TATCCTATTTAAGTA	2177
rs77582776	snp	C/T	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10069468	TAAGATGCCTCTCCC[C/T]CTCCCCCTCCCCCTC	2177
rs77646774	snp	C/T	0.00358779	0.0422022	intron-variant	FANCD2	GRCh38.p7	3:10057582	GTTGGCCAGGATGAT[C/T]TCAATCTCTTAACCT	2177
rs77683157	snp	C/T	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10048424	TTCTCCTGTCTCAGC[C/T]TCCTAAGTAGCTGTG	2177
rs77759895	snp	C/T			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10082507	AACTCTCTTACCTAG[C/T]CTCTAGGTCTTCTTC	2177
rs77921366	snp	A/G	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10047571	TCAAATTATAACCAA[A/G]GTGGAACATCCCTGG	2177
rs77957756	snp	C/T	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10047284	TTTCTGCCAATTATA[C/T]ATGTTTTGGGCTGTA	2177
rs78023816	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10027301	GTAGCAAACTCCCTT[A/G]GGGATAGGAGGAACA	2177
rs78035056	snp	A/G	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10047007	GAACTATCACTCTTT[A/G]GCCATTCAAAACTGT	2177
rs78121496	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10073609	ACTCCCTTTTTTGTA[C/T]CCCAGCAGTACATTG	2177
rs78196917	snp	G/T	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10047310	CTGTAATTTTCTAGA[G/T]GCAGAAACCACATGT	2177
rs78255811	snp	G/T	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10038596	TTTTTTTTTTTTTTT[G/T]TGAGACAGAGTCTTG	2177
rs78300723	snp	C/G	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10048496	TTTTAGTAGACACAG[C/G]GTTTCACCATGTTGG	2177
rs78402514	snp	A/G	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10047602	GGGTAGTATGATTGC[A/G]TGGGGAAACTGGGAT	2177
rs78434344	in-del	-/AA			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101078	TTTAAAAAAAAAAAA[-/AA]GTTTTAACAGTGATA	2177
rs78459965	snp	A/G	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10047625	ACTGGGATTTAGAAC[A/G]TCTGGCCTCCAATCC	2177
rs78520277	snp	A/G	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10047100	GAATAGTGTTTTGCC[A/G]GCTGAACGTTCAGGA	2177
rs78552151	snp	A/G	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10047431	CTATGTTTATTAACT[A/G]GTTATTTAGTCTGGG	2177
rs78628790	snp	A/G	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10046952	AGGGGAATAGGACCA[A/G]CCTGTAGAAACTAGT	2177
rs78641140	snp	C/G	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10047066	TGTAAATTATTCAAA[C/G]TGGAATTTTATAAGC	2177
rs78802160	snp	A/G	0	0	intron-variant	FANCD2	GRCh38.p7	3:10071147	AAAAAAAGAAAAAAA[A/G]AAAAAAAAAAAAAGA	2177
rs78859947	snp	C/T	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10048563	GCCTGCCTCAGCCTC[C/T]CAAAGTGCTGGGATT	2177
rs78896323	snp	A/C	0.00103735	0.0227508	FANCD2, FANCD2OS	3	allele_origin=A(germline)/C(germline)	3:10098930	CAAATGCTTCTATGC[A/C]CATTTCCATTCCCTC	2177
rs78941087	snp	C/T	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10048467	CACCACCACGCCCGG[C/T]TAATTTTTTGTATTT	2177
rs78988497	snp	C/T	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10048134	TTGTTGGTTGGAACT[C/T]ACTGAAGGGGAAGGA	2177
rs78993983	snp	C/T	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10048554	AGGTGAACCGCCTGC[C/T]TCAGCCTCTCAAAGT	2177
rs78994332	snp	A/G	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10047250	GTATTATTTTATCTT[A/G]CAGTTCTTTCTGTGT	2177
rs79038975	snp	A/G	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10047121	ACGTTCAGGATATTA[A/G]CAGTATAGAACTTAG	2177
rs79155092	snp	A/C	0	0	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10083889	CAAGACTCCGTCTCA[A/C]AAAAAAAAAAAAAAA	2177
rs79162593	snp	A/G	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10047485	AATTATTGGTAGGTT[A/G]TGATCACTTCTCTTC	2177
rs79194339	snp	C/T	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10047099	GGAATAGTGTTTTGC[C/T]AGCTGAACGTTCAGG	2177
rs79299475	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10024700	TTAAAAATTTCTTGC[A/G]GAATTTGCAAACTTC	2177
rs79368137	snp	G/T	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10048438	CTTCCTAAGTAGCTG[G/T]GATTACAGGCACACA	2177
rs79400344	snp	A/T	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10048545	CCTGACCTCAGGTGA[A/T]CCGCCTGCCTCAGCC	2177
rs79493774	snp	G/T	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10071969	AGTTCAAAACCAGCC[G/T]GACCAACATGGAGAA	2177
rs79512030	snp	A/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10082505	AAAACTCTCTTACCT[A/G]GCCTCTAGGTCTTCT	2177
rs79545295	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10030369	CCCAAAGTGCTGGGA[G/T]ATCGGACGTGAGCCA	2177
rs79617503	snp	G/T	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10046969	CTGTAGAAACTAGTA[G/T]AAATGTAAATATGTA	2177
rs79671520	snp	C/T	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10046964	CCAGCCTGTAGAAAC[C/T]AGTAGAAATGTAAAT	2177
rs79830642	snp	C/G	0.483444	0.0894635	intron-variant	FANCD2	GRCh38.p7	3:10048088	GGCAAGGAGGGAACA[C/G]AGAAAGGGAAAATAA	2177
rs79856812	snp	A/G	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10047482	TTGAATTATTGGTAG[A/G]TTATGATCACTTCTC	2177
rs79933580	snp	C/T	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10079922	TTCTTCTTCGTCTTC[C/T]TTTTTTTTTTTGAGG	2177
rs79961023	snp	A/G	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10048552	TCAGGTGAACCGCCT[A/G]CCTCAGCCTCTCAAA	2177
rs80104520	snp	C/T	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10047402	TTTTAAAAATTATGG[C/T]ATCAATAAGGAAGCT	2177
rs80125759	snp	C/T	0.5	0	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10086496	GGACCTTATATCTTC[C/T]TTTTTTTTTCTTTGA	2177
rs80128604	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10049577	GTGGGAAGGAGGTGA[A/G]ATGATGGGCAAGTAA	2177
rs80153629	snp	C/T	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10048594	ATAGGCGTGAGCCAT[C/T]GGGCCTGGCCGAGAC	2177
rs80187485	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10067771	CCACTGCACTCCAGC[C/G]TGGGTGACAGAGCGA	2177
rs80210301	snp	G/T	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10047234	AATAGATTTAACGGT[G/T]GTATTATTTTATCTT	2177
rs80258959	snp	G/T	0.0338695	0.125649	missense	FANCD2	GRCh38.p7	3:10067229	AAATGCCTTCTGCCA[G/T]GAAACATCACCTGAG	2177
rs80277271	snp	C/G	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10047440	TTAACTGGTTATTTA[C/G]TCTGGGTCCATTAAT	2177
rs80319361	snp	A/G/T	4.17672e-05	0.00456967	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087300	TTTTTTTTTTTTTTT[A/G/T]AATGAATAGGACTAA	2177
rs111326998	snp	G/T	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10049727	TTTCATGTTAAAGAC[G/T]AAGACACATAAGCAA	2177
rs111338639	in-del	-/A	0.330714	0.236612	intron-variant	FANCD2	GRCh38.p7	3:10030900	CAAGACTCTTATCTC[-/A]AAAAAAAAAAGGAAG	2177
rs111392584	snp	A/G	0.296619	0.245615	intron-variant	FANCD2	GRCh38.p7	3:10034307	TCCAGCCTAGGCAAC[A/G]GAACAAAACTCCATC	2177
rs111422104	in-del	-/C	0	0	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10086506	CTTCTTTTTTTTTTC[-/C]TTTGAGAGAGAGTCT	2177
rs111422914	snp	A/G	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10049956	CTGGTGCCCAAGTCA[A/G]TGGTGTGACTGAGGA	2177
rs111431131	in-del	-/G	0	0	intron-variant	FANCD2	GRCh38.p7	3:10041861	TTTTTTTTTTTCCCC[-/G]TCAATGAGTTTCAGA	2177
rs111469552	snp	A/C/G	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10047193	TAATGAGAATACCTC[A/C/G]CTGGGTCTTAAATTT	2177
rs111551651	snp	A/C	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10038494	GATAATTGAGCCAAC[A/C]TTTCTTTATTTATAA	2177
rs111589951	in-del	-/AA	0	0	intron-variant	FANCD2	GRCh38.p7	3:10060167	ACGAAAGTCCGTCTC[-/AA]AAAAAAAAAAAAAAA	2177
rs111688280	snp	A/G	0.5	0	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088273	GTTTATGTCTGGCAA[A/G]AGGGCCAGTGGATCA	2177
rs111738952	snp	A/G	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10061919	GGTGGTAATTGAACA[A/G]TGAGAACACATGGAC	2177
rs111782737	snp	G/T	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10031234	GGAGGCCAGGCACGG[G/T]GGCTCACGCCTGTAA	2177
rs111812387	in-del	-/T	0	0	intron-variant	FANCD2	GRCh38.p7	3:10040883	TCCTTTTGTATAGTC[-/T]TTTTTTTTTTTTAGC	2177
rs111898046	snp	C/G	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10077488	TGAACCTGGGACGCA[C/G]AGGTTGTAGTGAGCC	2177
rs111908971	snp	A/G			intron-variant	FANCD2	GRCh38.p7	3:10029082	AATATTATGATCTAG[A/G]CACATGCTATGTTAG	2177
rs111913511	snp	C/T	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10045100	ACTGTTTTTTTTTTT[C/T]TCCTGGAAGCATAGA	2177
rs112027741	snp	C/T	0.0667028	0.170006	intron-variant	FANCD2	GRCh38.p7	3:10054684	GAGTTGGGGTTTCAC[C/T]GTGTTAGCCAGGATG	2177
rs112029614	snp	C/G	0.00557542	0.0525036	upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10025078	CACACCTCAGCCTCC[C/G]GAGTAGCTGGGACTA	2177
rs112051825	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10054181	TGTGCCACTGCACTC[C/T]AGCCAGGGCAACAGA	2177
rs112070765	snp	C/T	0.0644693	0.167566	intron-variant	FANCD2	GRCh38.p7	3:10045110	TTTTTTTCCTGGAAG[C/T]ATAGACTCAGGTTGC	2177
rs112070870	snp	C/G			intron-variant	FANCD2	GRCh38.p7	3:10046125	GTGGCGCGATCTCGG[C/G]TCACTGTAAGCTCTG	2177
rs112071263	in-del	-/T/TT	0.305934	0.243663	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10084290	GCCACTACACCTGGC[-/T/TT]TTTTTTTTTTTTCTT	2177
rs112145845	in-del	-/TTTG	0.460589	0.13473	intron-variant	FANCD2	GRCh38.p7	3:10032657	GTGAAAATAATTCTA[-/TTTG]TTTGTTTGTTTTGGA	2177
rs112179204	snp	A/C/G	0.0442802	0.142054	intron-variant	FANCD2	GRCh38.p7	3:10067178	AAATCTGAACATTTG[A/C/G]AAGTATGAGAATGTA	2177
rs112220334	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10037429	TCAGGCATCGATTCG[A/G]AAGAGCAATAGATTG	2177
rs112249425	snp	C/T	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10028284	TTGTAACCCCAGCAC[C/T]TAGCACAGTCCCTAA	2177
rs112324505	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10069484	CTCCCCCTCCCCCTC[C/T]CCCTCTCCCGTCTCC	2177
rs112389812	snp	G/T			intron-variant	FANCD2	GRCh38.p7	3:10066565	CAAGTGCTGGACTCA[G/T]TTCTTTATGAAGAAA	2177
rs112406629	snp	A/T			intron-variant	FANCD2	GRCh38.p7	3:10054398	ATATATGTATATACG[A/T]ATATGTATATACGTA	2177
rs112418189	snp	A/G	0.0618563	0.164627	intron-variant	FANCD2	GRCh38.p7	3:10077023	CCCAAAGTACTGGGA[A/G]TTTGAGACCAGCCTG	2177
rs112421046	snp	C/G	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10075321	CCTGAGTAGCTGGGG[C/G]TATAGGCATCCGCCA	2177
rs112433757	snp	C/T	0.0566069	0.158427	intron-variant	FANCD2	GRCh38.p7	3:10044710	CCAATTTTGGGATGA[C/T]TATCTTAAAAGCTTT	2177
rs112438386	snp	A/G	0.00358779	0.0422022	intron-variant	FANCD2	GRCh38.p7	3:10053825	TCAGCTAACCATGAA[A/G]CTGTTCAGTTTCTGA	2177
rs112453789	snp	C/G/T	0.00795532	0.062565	intron-variant	FANCD2	GRCh38.p7	3:10069494	CCCTCCCCCTCTCCC[C/G/T]TCTCCCTCTGATGCC	2177
rs112487636	in-del	-/A	0	0	intron-variant	FANCD2	GRCh38.p7	3:10059809	GACTCCTTCTCAAAG[-/A]AAAAAAAAAAAAAGT	2177
rs112529037	snp	G/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10067855	GATGATTTATCCCAG[G/T]GATGCAAGGATTGTT	2177
rs112534969	snp	A/T			intron-variant	FANCD2	GRCh38.p7	3:10069470	AGATGCCTCTCCCCC[A/T]CCCCCTCCCCCTCCC	2177
rs112544276	snp	A/G	0.0759472	0.179459	intron-variant	FANCD2	GRCh38.p7	3:10045270	GCCTCCTGGGTTCAC[A/G]CCATTCTCCCGCTTC	2177
rs112626800	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10077836	GGAGTTTGAGACCAG[C/T]TTGGGCAATATAGTG	2177
rs112744109	in-del	-/A	0	0	intron-variant	FANCD2	GRCh38.p7	3:10039992	TATGGGATTTGACTT[-/A]AAAAAAAAAAGGTAT	2177
rs112776277	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10070523	GGGGTCAGCCCCCTG[C/T]CCGGCCAGCCGCCCC	2177
rs112820708	in-del	-/T	0.333491	0.235646	intron-variant	FANCD2	GRCh38.p7	3:10077333	AGGCTGAGACAGGCG[-/T]TATCACCTGAGGTCG	2177
rs112832879	snp	A/G	0.00034869	0.0131994	splice-acceptor-variant	FANCD2	GRCh38.p7	3:10043483	TCTCTGCTACTTGTA[A/G]TTCCTCAGGAAATCA	2177
rs112838104	snp	G/T	0.00119737	0.0244387	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10097472	CCATGCTGAGAAAAA[G/T]AATTCAGTGATATTT	2177
rs112847840	snp	C/T	0.295599	0.245806	intron-variant	FANCD2	GRCh38.p7	3:10059968	CTGAGGTCAGGAGTT[C/T]ACCAGCCTAGCCAAC	2177
rs112887807	snp	C/T	0.490307	0.068938	synonymous-codon	FANCD2	GRCh38.p7	3:10046615	TTTCATCATCTATAG[C/T]ACCAATACTCAGACA	2177
rs112895735	snp	A/C	0.00795532	0.062565	intron-variant	FANCD2	GRCh38.p7	3:10029689	ACCTGTCACCCGAAA[A/C]GTGTATGGTGTACCC	2177
rs112902928	snp	A/G	0.5	0	missense	FANCD2	GRCh38.p7	3:10048001	ATAATTTCATTTGGC[A/G]GTCTCCTATACAAAT	2177
rs112906586	snp	A/G/T			intron-variant	FANCD2	GRCh38.p7	3:10070484	TCTGCCGGGCCAGCC[A/G/T]CCCGGTCCGGGAGGG	2177
rs112934348	in-del	-/A	0	0	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10087539	TTCAAAAAAAAAAAA[-/A]TTTATCTGAGACATT	2177
rs112958263	snp	A/G	0.0205511	0.0992634	intron-variant	FANCD2	GRCh38.p7	3:10077717	ACAAAGTGAGACCCC[A/G]TCTGTATAAAAAAAT	2177
rs112979775	in-del	-/C	0	0	intron-variant	FANCD2	GRCh38.p7	3:10031861	TATGCCTTTTTTTTC[-/C]TTTGAGACAGAGTGT	2177
rs113006919	snp	A/T	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10048396	GCAACCTTCACCTCC[A/T]GGGTTCAAGCGATTC	2177
rs113017725	in-del	-/T	0	0	intron-variant	FANCD2	GRCh38.p7	3:10036684	TATTTCAAAACAGAA[-/T]TTTTTTTTTTTTTTT	2177
rs113043076	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10053370	ACATCACACTCTGGG[A/G]ACTTTGTGGGGTGGG	2177
rs113047424	in-del	-/TGTATTGA	0.057027	0.158938	intron-variant	FANCD2	GRCh38.p7	3:10045543	TTATTGAACCTTTCC[-/TGTATTGA]TGTATTGATGGGCAT	2177
rs113072264	snp	C/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10032748	GGACACATCAGTTTT[C/T]CTCTCATGATTATTA	2177
rs113076874	snp	A/G	0.00517822	0.0506191	intron-variant, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10027473	TCATGTGATTCAGGC[A/G]CTTCCCCCACCTCTG	2177
rs113097509	snp	C/G/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10050919	GGAGAAAGCCCTCCT[C/G/T]TACTAAAAATACAAA	2177
rs113107475	snp	C/T	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10032656	AGGTGAAAATAATTC[C/T]ATTTGTTTGTTTTGG	2177
rs113134644	snp	A/G	0.337386	0.23423	intron-variant	FANCD2	GRCh38.p7	3:10044602	AAAAGATAAAAAGCC[A/G]GATGATTGAGTTCCT	2177
rs113172818	snp	C/T	0.0209421	0.100162	intron-variant	FANCD2	GRCh38.p7	3:10045229	GCTGGACTGCACTGG[C/T]GTGATCTCGGCTCAC	2177
rs113192640	snp	C/T	0.5	0	synonymous-codon	FANCD2	GRCh38.p7	3:10042648	TCATTCCGTAACAGC[C/T]ATGGATACACTTGAG	2177
rs113246607	snp	A/G	0	0	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10089297	TCTCAAAAAAAAAAA[A/G]AATCATAATCACACT	2177
rs113250678	snp	C/T	0.5	0	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096390	CCCTGGAACTTTTAG[C/T]TTGCAGAGTCAAAGC	2177
rs113253588	in-del	-/ACT	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10074917	CCTTACATTTAGGTT[-/ACT]ACTACTACTACTACT	2177
rs113336560	snp	A/C/G			intron-variant	FANCD2	GRCh38.p7	3:10072549	CTCCCAAAGTGCTTG[A/C/G]GGTTACAGGCGCGAG	2177
rs113338938	snp	A/G	0.000149265	0.00863772	intron-variant	FANCD2	GRCh38.p7	3:10028612	TAACTTCTGTTTCCC[A/G]ATTTTGCTCTAGGAA	2177
rs113363588	snp	A/G	0.5	0	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094912	GAGAAAGGGAAGGTG[A/G]TATTTTATCCTAATG	2177
rs113381879	snp	A/T	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10075384	TAGAGACAGGGTTTC[A/T]CCATGTTAGCCAGGA	2177
rs113403330	snp	C/T	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10033218	GGAATTTGCGACCGG[C/T]CTGGGCAACACGTCT	2177
rs113408117	snp	G/T	0.0644693	0.167566	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10091165	GGCTCACTGCAGCCT[G/T]TGCCTTCTGGGCTCA	2177
rs113439931	in-del	-/AT	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10048861	AATTCTGTTATGACT[-/AT]TATGGAGTGACAGTA	2177
rs113441432	in-del	-/C	0.00159617	0.0282053	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10096014	ATTCTCTTAGCTAAA[-/C]AGGGCTACTCTATTG	2177
rs113466708	snp	C/T	0.00199481	0.0315187	intron-variant	FANCD2	GRCh38.p7	3:10053287	GCAAGAACAAAAAAC[C/T]GCACACCGCATATTC	2177
rs113469756	snp	A/G	0.5	0	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088381	CAATAATCATCCTCA[A/G]AAACCTGAAAAGCAA	2177
rs113512106	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101408	TTTTTTTTTTAAAGA[C/T]GGGGACTCGCTGTGT	2177
rs113549185	snp	A/C	0	0	intron-variant	FANCD2	GRCh38.p7	3:10076179	TATTCCACTGGGATC[A/C]CTCTGGGGTCCTGCC	2177
rs113549347	snp	A/G	0.0737376	0.17729	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10091478	CCCTGTCTCAAAAAG[A/G]AAAAAAAAAGAAAAA	2177
rs113574694	in-del	-/ACTA	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10047866	ACTCTTAGGTTGTGT[-/ACTA]ACTGTTTCCTACAGC	2177
rs113593713	snp	A/G	0	0	utr-variant-3-prime, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101606	GGCCAGATGGTCTCA[A/G]TCTCCTGAACTCATG	2177
rs113602719	snp	A/G	0.0603597	0.1629	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10084087	TAACCTCTGCTGCCC[A/G]GGTTCAAGCGATTCT	2177
rs113622283	snp	A/G	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10032657	GGTGAAAATAATTCT[A/G]TTTGTTTGTTTTGGA	2177
rs113623641	snp	A/G	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10042733	CTTCTCTGTCCCCAG[A/G]CTAACTGAGAATACT	2177
rs113633744	snp	A/G	0.311369	0.242351	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090776	GTTGCTGATTCTTCT[A/G]TGTCTTGGGTCCAAG	2177
rs113638061	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, upstream-variant-2KB	FANCD2, CIDECP	GRCh38.p7	3:10026538	CGGCCTAATCTCTAA[A/G]TCCGGGCCGCGGTCG	2177
rs113663828	in-del	-/G	0.333261	0.235728	intron-variant	FANCD2	GRCh38.p7	3:10034217	TAGTCCCAGCTACTT[-/G]GGGGGGCTGAGGCAG	2177
rs113688266	snp	A/G	0.33303	0.235809	intron-variant	FANCD2	GRCh38.p7	3:10078630	AAGTGCTGGGATTAC[A/G]GGCATGAGCCACCGC	2177
rs113697900	snp	A/G	0.00279162	0.0372561	intron-variant	FANCD2	GRCh38.p7	3:10080190	AGTGCTAGGATTACA[A/G]GCAAGAGCTACAGTG	2177
rs113698763	snp	C/G	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10069278	AGGGACTAATAACTG[C/G]AATATATAAAGATAG	2177
rs113706956	snp	C/G	0.5	0	intron-variant	FANCD2	GRCh38.p7	3:10048993	ACTATATGGAGAAAA[C/G]CTTTAAAGCTTTTAG	2177
rs113771705	snp	C/T	0.29789	0.24537	intron-variant	FANCD2	GRCh38.p7	3:10034299	CACTGCACTCCAGCC[C/T]AGGCAACAGAACAAA	2177
rs113788167	snp	C/G/T			intron-variant	FANCD2	GRCh38.p7	3:10070488	CCGGGCCAGCCTCCC[C/G/T]GTCCGGGAGGGAGGT	2177
rs113873284	snp	C/T	0	0	intron-variant	FANCD2	GRCh38.p7	3:10045101	CTGTTTTTTTTTTTT[C/T]CCTGGAAGCATAGAC	2177
rs113890152	snp	A/G	0.298398	0.245271	intron-variant	FANCD2	GRCh38.p7	3:10044302	GACTAGAGTAAATCA[A/G]TCTGTCCACTGTCAA	2177
rs113930338	snp	C/T	0.5	0	synonymous-codon, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092244	AGTATCCTCATCAAC[C/T]TGATAAAGGTGAGTA	2177
rs114101942	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10047813	AAGTTAAAATGAGAG[C/T]TAGGGAGGAGAAGTC	2177
rs114108275	snp	C/T	0.00755907	0.0610114	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10094518	ATTGGACTGAATATT[C/T]CAAAGTAGGCTGAAC	2177
rs114109836	snp	A/G	0.0566069	0.158427	intron-variant	FANCD2	GRCh38.p7	3:10059903	GGGCTGGGTATGGTG[A/G]TTCACACCTGTAATC	2177
rs114362791	snp	A/C	0.0566069	0.158427	intron-variant	FANCD2	GRCh38.p7	3:10068279	CTATTAGATAAATTC[A/C]GTAAAGTTGCAAGAT	2177
rs114395370	snp	A/T	0.0162398	0.0886349	intron-variant	FANCD2	GRCh38.p7	3:10029187	AAATAGTTGACAAAG[A/T]TCCCAAGAGTTCCAG	2177
rs114554709	snp	C/T	0.0376037	0.131863	intron-variant	FANCD2	GRCh38.p7	3:10029231	ATGGCTGGGTGCTAT[C/T]GCTCACACCTGTAAT	2177
rs114848937	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10086282	ACTGATAGCCTGTTT[C/G]TTTCCCCTTGTCTTG	2177
rs115159701	snp	A/G	0.0154538	0.0865337	intron-variant	FANCD2	GRCh38.p7	3:10069197	ctctgcatagcaaag[A/G]aaacaccaaagtgaa	2177
rs115236195	snp	C/G	0.00279162	0.0372561	intron-variant	FANCD2	GRCh38.p7	3:10079890	TATATCCCGTTTCTT[C/G]GTTTCTTGATTCATT	2177
rs115247173	snp	A/G	0.00511523	0.0503135	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090270	TCATGGTGTGGGCAC[A/G]CATGCTTTTCCCGTC	2177
rs115303265	snp	C/T	0.00398564	0.0444627	intron-variant	FANCD2	GRCh38.p7	3:10069231	ACAGCCCACAGAATG[C/T]GAGAAAATATTTGCA	2177
rs115349693	snp	G/T	0.00279162	0.0372561	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10083985	GTATATTCTAAACTT[G/T]TTTCCCATGCTTTTG	2177
rs115393988	snp	C/T	0.0154538	0.0865337	intron-variant	FANCD2	GRCh38.p7	3:10061080	TGCAGCCCTCCTGCG[C/T]CCAACTTAATCACCA	2177
rs115405316	snp	C/T	0.0146672	0.084371	intron-variant	FANCD2	GRCh38.p7	3:10075028	AACATTTGTTCAGCA[C/T]CTGACAGTTGCTTAC	2177
rs115447266	snp	A/C	0.0154538	0.0865337	intron-variant	FANCD2	GRCh38.p7	3:10041218	AAACAAACAAACAAA[A/C]AAAAAAGCAATCTAT	2177
rs115497679	snp	A/G	0.0154538	0.0865337	intron-variant	FANCD2	GRCh38.p7	3:10068308	ATACAAAATCATCAT[A/G]TAAAAATGAGTAGCA	2177
rs115630604	snp	C/T	0.00279162	0.0372561	upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10024405	ATAGATTCTTAAGAA[C/T]ATGGAACTCTGGTTT	2177
rs115813235	snp	A/G	0.0138799	0.0821421	intron-variant	FANCD2	GRCh38.p7	3:10076092	AGGAGATGCCACATA[A/G]ATGTGTATTGAGTGA	2177
rs116207455	snp	A/G	0.00953873	0.0683987	downstream-variant-500B, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10102010	ATTGAGATTTGTGCA[A/G]AGAAATTATGGAGAC	2177
rs116321370	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	FANCD2, CIDECP	GRCh38.p7	3:10024922	GAACAAGTGTTTTTT[C/T]GTTTGTTTTTCTGGA	2177
rs116340149	snp	C/T	0.00636936	0.0560724	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10084682	ACCAAAAACCTGACA[C/T]CTAATAGGCCCTCAG	2177
rs116398158	snp	A/G	0.00318978	0.0398085	intron-variant	FANCD2	GRCh38.p7	3:10056593	CTGCAGTGCAGTGGC[A/G]TGATCATACTTCACT	2177
rs116621886	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10047796	AAAGATTAAGATTTC[C/T]TAAGTTAAAATGAGA	2177
rs116635111	snp	A/G	1.67742e-05	0.002896	intron-variant	FANCD2	GRCh38.p7	3:10052340	TTTGAATTTTAAGGG[A/G]AAAATGTTAGCTGCT	2177
rs116736407	snp	C/G	0.000531244	0.0162892	missense	FANCD2	GRCh38.p7	3:10043147	AAAGTAAAGGACGAG[C/G]AAGGTAAAGAGCTCA	2177
rs116832443	snp	C/T	0.0150606	0.0854603	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10092482	TATGCCACAATACTA[C/T]TTAATGACTCCTTCC	2177
rs116922603	snp	A/G	0.00953873	0.0683987	intron-variant	FANCD2	GRCh38.p7	3:10050343	TAAGAATATGTGGCG[A/G]TCCGGGTGCGGTGGC	2177
rs116962388	snp	C/T			intron-variant	FANCD2	GRCh38.p7	3:10067151	TCTGGATAAATAATA[C/T]AAACAAGGTTAAAAT	2177
rs117017234	snp	A/G	0.0263992	0.111815	intron-variant	FANCD2	GRCh38.p7	3:10071301	TCCTCAAAAAACTAA[A/G]AATAGAATCACCATA	2177
rs117037473	snp	A/C	0.000798403	0.0199641	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10080859	TTTATCTGATTAGTT[A/C]TGATAGGGCTATATG	2177
rs117408636	snp	A/T	0.00159617	0.0282053	intron-variant	FANCD2	GRCh38.p7	3:10041824	TTGAAACCATAGTGA[A/T]TCACATTTGATATCT	2177
rs117703947	snp	A/T	0.00279162	0.0372561	intron-variant	FANCD2	GRCh38.p7	3:10037330	CAGTAAAATAAATGC[A/T]TTTTTTCCTACTCTC	2177
rs117901192	snp	C/T	0.00318978	0.0398085	intron-variant	FANCD2	GRCh38.p7	3:10059151	TCCGAGTAGCCAGGA[C/T]CACAGGCATGCACCA	2177
rs121917786	snp	A/G	4.97855e-05	0.00498902	FANCD2, FANCD2OS	3	allele_origin=G(germline)/A(germline)	3:10090315	TTGTTGTTTTCTTCC[A/G]TGTGATGATGGCTGA	2177
rs121917787	snp	C/T			missense	FANCD2	GRCh38.p7	3:10043065	GTAATTTCTGAGCTT[C/T]GGGAGAAGTTGGATC	2177
rs121917788	snp	C/T			stop-gained	FANCD2	GRCh38.p7	3:10043119	CGGTTACAGGCTTCC[C/T]AAGTAAAGTTGAAAA	2177
rs137916747	snp	A/G	0.0023933	0.0345097	intron-variant	FANCD2	GRCh38.p7	3:10068109	TATAATACCACTATT[A/G]TAAAATACAGTATTG	2177
rs137922964	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10041127	TGAGCGTGGAAGGTC[A/G]AAGCTACAGTGAGCT	2177
rs137927195	snp	A/G	0.0154538	0.0865337	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10098158	GCACCACAGAGAATT[A/G]GCTTCCTTTCTTCAC	2177
rs138111025	in-del	-/A			utr-variant-3-prime, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10101402	TTTTTTTTTTTTTTT[-/A]AAAGACGGGGACTCG	2177
rs138115961	snp	A/C	0.00279162	0.0372561	intron-variant	FANCD2	GRCh38.p7	3:10073150	ATAAAATTACCTCTT[A/C]TACCTCTAGGCAGTT	2177
rs138155691	in-del	-/T	0.372391	0.217992	intron-variant	FANCD2	GRCh38.p7	3:10076036	GCGCCCAGCCATATC[-/T]TTTTTTTTTTTTTTT	2177
rs138183965	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10030633	GGCCGGGCACAGTGG[C/T]TCACACCTGTAATCC	2177
rs138189144	snp	C/G	0.000856319	0.0206743	synonymous-codon	FANCD2	GRCh38.p7	3:10064412	CTTCGTAGTGGACTC[C/G]TGTGTTGTTCCGGAA	2177
rs138189159	snp	A/T	0.000313069	0.0125075	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088399	ACCTGAAAAGCAAGA[A/T]TGAGGTCAAGTTCCC	2177
rs138242590	snp	C/T	0.0154538	0.0865337	intron-variant	FANCD2	GRCh38.p7	3:10077299	CAGTGGCTCACGCCT[C/T]TAATCACAGCACTTT	2177
rs138283015	snp	A/G	0.292008	0.246445	intron-variant	FANCD2	GRCh38.p7	3:10050853	GCACTTTGGGAGGCC[A/G]AGGCGGACGGATCAC	2177
rs138347896	snp	A/G	0.299411	0.245069	intron-variant	FANCD2	GRCh38.p7	3:10054361	TATATACGTATATAT[A/G]TATATACGTGTATAT	2177
rs138377091	snp	A/T	0.00914312	0.0669923	intron-variant	FANCD2	GRCh38.p7	3:10044329	TCAAGGCAGTGGTAC[A/T]GGATCTTATGTCTCT	2177
rs138398760	snp	A/G	0.000263661	0.0114787	missense, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10093312	CATCCTGTTCTGCAT[A/G]TATGTTTGAAGGTGA	2177
rs138409505	snp	A/G	3.29538e-05	0.00405904	synonymous-codon, intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088525	CATCTCTAATGACCA[A/G]CTCCATGCTCTGCTC	2177
rs138480262	snp	A/C	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10090542	TCGGCTCACTGCAAC[A/C]TCACCTCCTGGGTTC	2177
rs138520747	snp	A/G	0.000153988	0.00877328	splice-acceptor-variant	FANCD2	GRCh38.p7	3:10067207	TAATTTGTACTTTGC[A/G]GATTGTAAATGCCTT	2177
rs138587722	snp	G/T	9.8837e-05	0.00702914	missense	FANCD2	GRCh38.p7	3:10042583	TTGGTGATGGATAAG[G/T]TGTCGTCTATTAGAT	2177
rs138608475	snp	A/T	1.64754e-05	0.00287009	missense	FANCD2	GRCh38.p7	3:10035232	GGATTGACATACTGC[A/T]GGTAAGACTGTCACT	2177
rs138608601	snp	C/G	0.00676609	0.0577691	intron-variant	FANCD2	GRCh38.p7	3:10067376	TGAGGCAATAAAGCA[C/G]TTAGCTTTCCCTGAT	2177
rs138668703	snp	A/G	0.0146672	0.084371	intron-variant	FANCD2	GRCh38.p7	3:10076695	TCTAGGGCCACTGGC[A/G]TGCCCCACTACACCC	2177
rs138849770	snp	A/C	0.00557542	0.0525036	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10081944	TTAAATACTTTTGTT[A/C]CTCAGGGACAGGCGT	2177
rs138892285	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10084686	AAAACCTGACACCTA[A/G]TAGGCCCTCAGAATA	2177
rs138930007	snp	A/T	0.000798403	0.0199641	intron-variant	FANCD2	GRCh38.p7	3:10060808	AAGATCTTGTGTATT[A/T]CCCCTCACCTTGTTC	2177
rs138960268	snp	A/G	0.00398564	0.0444627	intron-variant	FANCD2	GRCh38.p7	3:10041055	AAAAATTAGGTGGGC[A/G]TGGTGGTACGCACTT	2177
rs139025231	snp	C/T	0.000115702	0.00760509	missense	FANCD2	GRCh38.p7	3:10032889	ATATTGCTAATGAAG[C/T]TGAAGAAAATGACAG	2177
rs139033444	snp	A/G/T	0.000889391	0.0210723	synonymous-codon	FANCD2	GRCh38.p7	3:10064810	CATAAACCTCCTGCC[A/G/T]CTGCTGTTTTCTCAG	2177
rs139084322	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10058544	ATTTTAAGGATTTAA[C/T]GTCATTCTTTTGCAC	2177
rs139107010	snp	C/T	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10036486	ATTTTACTGGAGTGT[C/T]TTTGAAGTTTCATCT	2177
rs139114811	snp	C/G			intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10095786	CAGAACCCTAGAGTT[C/G]TGCAGTCACTGGCAA	2177
rs139190448	snp	C/T	0.00119737	0.0244387	intron-variant	FANCD2	GRCh38.p7	3:10062778	TGCGGTGGTGCTTCC[C/T]GGGTTCAAGCAATTC	2177
rs139397618	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10088675	TTAAAAATGAACACA[A/G]TTTGGAACATGTGGA	2177
rs139435401	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10082365	AACCTGGACTGGGCT[A/G]GGTTCACACTTGGCC	2177
rs139532890	snp	A/G	0.000399281	0.0141238	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10083607	AAGCATACGTCCACC[A/G]ACCAGGCGCAGTGGC	2177
rs139600289	snp	C/T	0.0314385	0.121371	intron-variant	FANCD2, FANCD2OS	GRCh38.p7	3:10086468	AGTGCTTATCATCCC[C/T]GTCTATAGGTCAGGA	2177
rs139604883	snp	C/G	0.000399281	0.0141238	intron-variant	FANCD2	GRCh38.p7	3:10036775	AATGGTAGTTGTCTC[C/G]AAAGAGGGTAGCCAG	2177
rs139619722	in-del	-/T			intron-variant	FANCD2	GRCh38.p7	3:10073612	CCTTTTTTGTACCCC[-/T]AGCAGTACATTGAAT	2177
rs139676351	in-del	-/A	0.00199481	0.0315187	intron-variant	FANCD2	GRCh38.p7	3:10037852	TGCAATAAGTAGTTC[-/A]GTATTTTGTTTAAAA	2177
rs139729777	snp	A/G	0.329317	0.237084	intron-variant	FANCD2	GRCh38.p7	3:10044399	TTGGCCGGGCGCGGT[A/G]GCTCACGCCTATAAT	2177

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